iUUCD 2.0 - integrated annotations for ubiquitin and ubiquitin-like conjugation database

LNX1

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs62325512	snp	A/T	0.0310518	0.120672	intron-variant	LNX1	GRCh38.p7	4:53642358	TTTAAAATGTATACA[A/T]GCTTTTGAACATATT	84708
rs66686407	in-del	-/TGTT			intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53462356	AGGTACAGGCCAAGT[-/TGTT]GTTAACTATGTTATA	84708
rs66696444	in-del	-/G			intron-variant	LNX1	GRCh38.p7	4:53491801	ACGATACTTTTTTTT[-/G]GTTTGTTTGTTTTTT	84708
rs66944126	snp	A/T	0.482831	0.0910472	intron-variant	LNX1	GRCh38.p7	4:53612517	ATAAATTATGGCATA[A/T]CCATATGATGGAAAA	84708
rs67041466	snp	A/G	0.479095	0.100076	intron-variant	LNX1	GRCh38.p7	4:53612618	TGAGCCTAGGAGTTC[A/G]AAACTGGCCTGGGCA	84708
rs67043790	in-del	-/CT			intron-variant	LNX1	GRCh38.p7	4:53475072	ACACCCAGCCCAGAC[-/CT]TACTTCCAGCAAAAG	84708
rs67069112	in-del	-/ACAGAAGTAG			intron-variant	LNX1	GRCh38.p7	4:53590516	TTGGGCTGTCAAGAT[-/ACAGAAGTAG]ACAGGCTGTGTGATC	84708
rs67415683	multinucleotide-polymorphism	AA/GC	0.5	0	intron-variant	LNX1	GRCh38.p7	4:53649344	TGTCAATCCCACAAG[AA/GC]GACTACTATTACAAT	84708
rs67587333	in-del	-/G			intron-variant	LNX1	GRCh38.p7	4:53491809	TTTTTTTTTTTTTTT[-/G]TTTTTTGAGAAAAGT	84708
rs68028807	snp	A/G	0.0456336	0.143994	nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53604689	CCAAAAATGAATTAT[A/G]AATATCAGTCCAAAG	84708
rs68056217	snp	A/C	0.390277	0.206936	intron-variant	LNX1	GRCh38.p7	4:53472700	CAAAAAAAAAAAAAA[A/C]AAAAAACAATGGGGA	84708
rs68099236	snp	A/G	0	0	intron-variant	LNX1	GRCh38.p7	4:53528685	CCTGTGGATAAGGGG[A/G]GGACTACTGTATAGC	84708
rs68111012	in-del	-/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53595976	CATCTCTACAAAAAC[-/G]CTCTTTGGCTATCTT	84708
rs68134111	multinucleotide-polymorphism	AT/GG	0	0	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53510103	AAAGATGCACCCAAG[AT/GG]AATTAAAAGTGGTGT	84708
rs71197029	in-del	-/TT			intron-variant	LNX1	GRCh38.p7	4:53545824	ACTTCAGAGGCCACA[-/TT]TTTTTTTTTTTTTTT	84708
rs71197031	in-del	-/GGGCACAAGACAGGG	0	0	intron-variant	LNX1	GRCh38.p7	4:53568610	GGGCACAAGACAGGG[-/GGGCACAAGACAGGG]ATGCCCTCTCTCACC	84708
rs71197033	in-del	-/AT	0.5	0	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53594156	TATATATATATATAT[-/AT]GTATATATAAATATG	84708
rs71197034	in-del	-/T	0	0	intron-variant	LNX1	GRCh38.p7	4:53612705	GTATTTTTTTTTTTT[-/T]GTAGAGATGGGGTCT	84708
rs71197035	in-del	-/GTCA	0	0	intron-variant	LNX1	GRCh38.p7	4:53616723	CTTATCAATATGCCA[-/GTCA]TTCACTTTAATTAAT	84708
rs71597842	snp	A/G	0.5	0	intron-variant	LNX1	GRCh38.p7	4:53472778	AGGTGTATGAAAGCA[A/G]ATATAGAGGCCAAGC	84708
rs71597843	snp	A/G	0.5	0	intron-variant	LNX1	GRCh38.p7	4:53472849	GAAATGAGTGTTCCA[A/G]AGAGTTGTTATATTG	84708
rs71597844	snp	A/C	0.5	0	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507549	TCTGATAAGATATAC[A/C]CAATAAGACATTAAC	84708
rs71597845	snp	A/C	0.5	0	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507563	CACAATAAGACATTA[A/C]CAGTGACTACCTCTG	84708
rs71597846	snp	A/G	0.104504	0.2033	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53516056	AGGAGTTAGAGACCC[A/G]TAGCAGGACCCATAT	84708
rs71597847	snp	A/C	0.5	0	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53521062	CTGGGCTATGGATCA[A/C]CGGTGCTTTCTATTT	84708
rs71597849	snp	A/G	0.499325	0.0183582	intron-variant	LNX1	GRCh38.p7	4:53570095	TTCAACCATTGTGGA[A/G]GTCAGTGTGGCGATT	84708
rs71639504	multinucleotide-polymorphism	CA/TG	0	0	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53513277	ATGTATTATGCTTTA[CA/TG]GATGTGGTCTCATTT	84708
rs71662228	in-del	-/AATT	0.338069	0.233974	intron-variant, downstream-variant-500B, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460056	GGCCTCTATGAAATA[-/AATT]AATTAATTACCCATA	84708
rs71662229	in-del	-/GAA	0.432797	0.170544	intron-variant	LNX1	GRCh38.p7	4:53463638	AAATTTAGGCCTATC[-/GAA]GAAGATTTGGCATAG	84708
rs71662232	in-del	-/CTAT	0.5	0	intron-variant	LNX1	GRCh38.p7	4:53479639	AAAGAGATGACTTTT[-/CTAT]CTATCTTTTTTCGCC	84708
rs71662233	in-del	-/AGTA	0.250732	0.249999	intron-variant	LNX1	GRCh38.p7	4:53490521	CCCAGGCTGCTGCTG[-/AGTA]AGTAAGCTGAGGTTA	84708
rs71662234	in-del	-/C	0.5	0	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53505290	TTTGAGATGGAGTCA[-/C]CCCAGGCTGGAGTGC	84708
rs71662235	in-del	-/G	0.5	0	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53505294	AGATGGAGTCACCCA[-/G]GGCTGGAGTGCAGTG	84708
rs71662236	in-del	-/GT	0.5	0	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53512487	CCCTACCCAGTGTTT[-/GT]GTGTGTGTGTGTGTG	84708
rs71662238	in-del	-/G			intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53574982	TCCATTAGATATTTC[-/G]TTTTTTTTTTTTCTT	84708
rs71662240	in-del	-/GT	0.5	0	intron-variant	LNX1	GRCh38.p7	4:53625844	CAGCAATTCCACCCC[-/GT]GTGTGTGTGTGTGTG	84708
rs71928074	in-del	-/TCT			intron-variant	LNX1	GRCh38.p7	4:53536331	ATTCTCACTCCACAT[-/TCT]CTTCAAGAGGGGACT	84708
rs72489917	in-del	-/GA			intron-variant	LNX1	GRCh38.p7	4:53492533	GAGAGAGAGAGAGAG[-/GA]AGAGAGAGAGTGGCA	84708
rs72599380	in-del	-/TTC			intron-variant	LNX1	GRCh38.p7	4:53536334	CTCACTCCACWTCTT[-/TTC]CAAGAGGGGACTTTT	84708
rs72599381	in-del	-/AA			intron-variant	LNX1	GRCh38.p7	4:53541145	TAACTCAAAAAAAAA[-/AA]ARRAAAAAAAAAAAG	84708
rs72599384	in-del	-/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53595974	GTCATCTCTACAAAA[-/G]ACCTCTTTGGCTATC	84708
rs72624195	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53490096	CTGTTGTCAAATGTT[C/T]TTTGATGAAATGAAT	84708
rs73145476	snp	A/G	0.00517822	0.0506191	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53516264	TAAAAAAAGAATCAC[A/G]CAAAATGCCAAACAG	84708
rs73145478	snp	A/C	0.23846	0.249734	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519853	TTGCGCAGTTTGCAT[A/C]TAGGGTGACCAACCA	84708
rs73145486	snp	A/C	0.0138799	0.0821421	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53522726	ATTGAGGCTCAGAGA[A/C]GAAACTTTTTAGAAT	84708
rs73145488	snp	C/T	0.040671	0.13668	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53522820	AAAACCAAAACCAAA[C/T]CAAACCAAACCAAAA	84708
rs73145499	snp	A/C	0.0248432	0.108648	intron-variant	LNX1	GRCh38.p7	4:53531636	TATAAGCCTGGGGTG[A/C]ATGTAAAGGGAGGTG	84708
rs73145501	snp	C/T	0.0437281	0.141251	intron-variant	LNX1	GRCh38.p7	4:53533261	AGGTCCAATAGAACA[C/T]ACAAAGGAACCAGAT	84708
rs73147405	snp	C/T	0.0134861	0.0810011	intron-variant	LNX1	GRCh38.p7	4:53537713	TACCATTTCCCCATC[C/T]GTCATTAGGCTGTGC	84708
rs73147411	snp	A/G	0.270621	0.249148	intron-variant	LNX1	GRCh38.p7	4:53544140	ATAGACTATCTAGGT[A/G]TTTGAGAGCAGTACA	84708
rs73147477	snp	C/T	0.240478	0.249819	intron-variant	LNX1	GRCh38.p7	4:53561438	TCACTGTGTTGGCCA[C/T]GATGGTCTTGATCTC	84708
rs73147485	snp	A/G	0.309154	0.242901	intron-variant	LNX1	GRCh38.p7	4:53584009	TTTTTGCATTGATTC[A/G]GAGCTCTGTTCATGC	84708
rs73147488	snp	C/T	0.0107246	0.0724382	intron-variant	LNX1	GRCh38.p7	4:53585345	TCCTTGCCTGTACTT[C/T]GCTCAGTATTTCAGC	84708
rs73147489	snp	C/T	0.0197687	0.0974348	intron-variant	LNX1	GRCh38.p7	4:53589911	GCTGACATACAGTGA[C/T]GAAATTATTTATTTA	84708
rs73147490	snp	A/G	0.0197687	0.0974348	intron-variant	LNX1	GRCh38.p7	4:53590228	TCTGTCTAAGGCAAA[A/G]ATGATCTCAGCTTGT	84708
rs73147492	snp	A/T	0.0185938	0.0946107	utr-variant-5-prime, upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53591443	GCAGGCAGCTCTCAT[A/T]CCTTGTGGGTGAACC	84708
rs73147495	snp	C/G	0.0185938	0.0946107	upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53591761	GCACGTGTCCAGCCC[C/G]GTGTTCAGATCTGAA	84708
rs73147498	snp	C/G	0.0185938	0.0946107	upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53592191	TACGGCAGTTACAGT[C/G]CACTGCAGGCCTGCA	84708
rs73147500	snp	C/T	0.0283406	0.115616	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53602589	ACCTCCTATAATGGG[C/T]GGTCTGTGAGGGCAC	84708
rs73149325	snp	A/G	0.0689305	0.172377	intron-variant	LNX1	GRCh38.p7	4:53617136	TCTAAAGGGACTTAC[A/G]CTATTTTGAAGAGAC	84708
rs73149387	snp	A/G	0.0325976	0.123435	intron-variant	LNX1	GRCh38.p7	4:53617769	TTGACTAAACCTGTA[A/G]CAACTGGGTTTGTCT	84708
rs73149389	snp	C/T	0.0325976	0.123435	intron-variant	LNX1	GRCh38.p7	4:53618821	TATTAAACATGTATT[C/T]ACATATTTATGTCCC	84708
rs73149391	snp	C/T	0.0876345	0.190099	intron-variant	LNX1	GRCh38.p7	4:53619585	TCCATTGTAAGGGTA[C/T]ACAGCACATGTTGTT	84708
rs73151316	snp	C/T	0.0103295	0.0711199	intron-variant	LNX1	GRCh38.p7	4:53629112	ATAAACCACTTGTAC[C/T]CCCAAAGCTATTGAA	84708
rs73151321	snp	C/T	0.0755793	0.179102	intron-variant	LNX1	GRCh38.p7	4:53630131	TAACAACCATGTAAG[C/T]TTTCCCTTTACCCTG	84708
rs73151327	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53638194	TAACTTTTGATTATT[C/T]CTCTGACTTGGCTTC	84708
rs73157815	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53462015	CTTTGAATAATCTCA[A/G]TGAAAGCAGTTTAAG	84708
rs73157877	snp	A/G	0.0322114	0.122752	intron-variant	LNX1	GRCh38.p7	4:53494496	GGAGAACTCCAGCTC[A/G]TTCCTCAAGCCCCAA	84708
rs73250968	snp	A/G	0.0142736	0.0832652	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498431	TTTATATACAGAGAG[A/G]AAGGGGGGAGAGAGT	84708
rs73250969	snp	A/G	0.187685	0.242109	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53502419	AGTGTACAATAGCAT[A/G]TTTTTTAAAATGTAC	84708
rs73250970	snp	A/G	0.0193772	0.0965046	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53511014	GGGTTCTAAAGATAA[A/G]TTTTTGAGTCCAGGA	84708
rs73250971	snp	C/T	0.0437281	0.141251	intron-variant	LNX1	GRCh38.p7	4:53534331	CCTGAATGTCATAAA[C/T]TGATATAAGGAGAGC	84708
rs73250972	snp	C/T	0.079617	0.182947	intron-variant	LNX1	GRCh38.p7	4:53587877	AGGCATTTCCACTGG[C/T]AGCCACTCTACCCTG	84708
rs73250973	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53590252	AGCTTGTTTCAATTC[A/G]TACCTTGGGAGAATT	84708
rs73250974	snp	A/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53594311	CTTGAGGGACCCCTC[A/G]AGAATGACCAGTTGT	84708
rs73250975	snp	A/T	0.370974	0.218781	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53605650	ATTCATGTTTTTTTT[A/T]AAATTCCATATATAA	84708
rs73250976	snp	C/T	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53642460	GGACAAAGGGTCTCC[C/T]GGCCATTGACCACTT	84708
rs73250977	snp	G/T	0.0562307	0.157967	intron-variant	LNX1	GRCh38.p7	4:53646554	CCAATCTACATTTTT[G/T]GCTGAGTGAATGAAC	84708
rs73816216	snp	C/T	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53589481	TCTCCTCCAAGCAAC[C/T]TAGGAAAATTCCTTC	84708
rs73816562	snp	C/T	0.185472	0.241529	intron-variant	LNX1	GRCh38.p7	4:53542490	CAAAGAGTGTCCTAA[C/T]AATCACCATCACATT	84708
rs73816883	snp	G/T	0.5	0	intron-variant	LNX1	GRCh38.p7	4:53486723	AAACTAAGTAGCGTC[G/T]GTATGGAAGGACTGG	84708
rs73816885	snp	A/G	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53493922	TCCAAGAATGCCCCC[A/G]TGGCTTTGCGGATAA	84708
rs73816893	snp	C/T	0.00795532	0.062565	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53506086	TGGTTTGGGTTCTGC[C/T]TCCCAACTCCCAAGA	84708
rs73818505	snp	A/G	0.00676609	0.0577691	intron-variant	LNX1	GRCh38.p7	4:53564447	AGGGGATGAGGAGGA[A/G]TGGCTGGGTTTTCAC	84708
rs73818511	snp	A/G	0.00636936	0.0560724	intron-variant	LNX1	GRCh38.p7	4:53589223	CAGGATGAGAGCCTT[A/G]GAGTGGGAAAAGGAA	84708
rs73818919	snp	G/T	0.0138799	0.0821421	intron-variant	LNX1	GRCh38.p7	4:53524871	TTCTTTGCAAAAAAA[G/T]CTCTGTCTGCTTGCC	84708
rs73818920	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53526957	ATCATTATGCTAAAG[C/T]AATAGAAATGAAACA	84708
rs74347547	snp	A/C	0.101658	0.201233	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53516966	GAACTGCTGCCCCTG[A/C]CTGCCAGTCACACTC	84708
rs74364256	snp	G/T	0.5	0	intron-variant	LNX1	GRCh38.p7	4:53582932	CAAATGGTGGCCTCA[G/T]CTCTCTTTCTAAAAT	84708
rs74366481	snp	G/T	0.449218	0.151037	intron-variant	LNX1	GRCh38.p7	4:53471023	accaaaaaagagccc[G/T]cattgccaagtcaat	84708
rs74393931	snp	C/T	0.5	0	intron-variant	LNX1	GRCh38.p7	4:53491792	GCTGAGGATACGATA[C/T]TTTTTTTTGTTTGTT	84708
rs74488918	in-del	-/AAAA			intron-variant	LNX1	GRCh38.p7	4:53610730	GAAAAAAAAAAAAAA[-/AAAA]GAAATAAACCAAATC	84708
rs74551202	snp	C/T	0.00557542	0.0525036	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53502097	ATTTGTTCAATATTA[C/T]GTCCTCACTCAAGGA	84708
rs74568157	snp	A/T			missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507334	TCAGGGGCAGTGGTG[A/T]TTTCAGAATTTTCCC	84708
rs74575329	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53603414	AGCTGGGTTATAGGC[A/G]GGGTGGATATGCAGC	84708
rs74599218	snp	C/T	0.02016	0.0983543	utr-variant-5-prime	LNX1	GRCh38.p7	4:53652357	CCTGGGCATCCCCTG[C/T]CCCTTCTGCAAGGCT	84708
rs74628866	snp	C/T	0.0189856	0.0955633	intron-variant	LNX1	GRCh38.p7	4:53463511	TAAGTTGGGTTATTT[C/T]ACTCCCCACTGGGAA	84708
rs74658403	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53476056	AATCCCAGCACTTTG[C/T]CAGGCCGAGGCAGGC	84708
rs74687349	snp	A/G	0.444444	0.157135	intron-variant	LNX1	GRCh38.p7	4:53470015	CATCATCCTGATACC[A/G]AAGCCGGGCAGAAAC	84708
rs74714929	snp	A/G	0.0209421	0.100162	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53605406	TGCATCATCTTACAT[A/G]GTAACTACCTTGTGT	84708
rs74717127	snp	C/T	0.0205511	0.0992634	intron-variant	LNX1	GRCh38.p7	4:53640227	TATTAAAAACAAGAA[C/T]GACTGTCAGGAAGGC	84708
rs74765964	snp	C/G	0.00676609	0.0577691	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53505617	AGGAAGAGACTGGTG[C/G]AAAGGAAGTTCTAAT	84708
rs74794020	snp	C/T	0.449345	0.150869	intron-variant	LNX1	GRCh38.p7	4:53471029	aaagagcccgcattg[C/T]caagtcaatcctaag	84708
rs74866954	snp	A/G	0.27278	0.24896	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53516022	TTGATAGGCTGGGGT[A/G]GAAAGATCACTTGAA	84708
rs74880941	snp	A/T	0.1652	0.235179	intron-variant	LNX1	GRCh38.p7	4:53649497	GAGCTCTTGTCCTGA[A/T]GTCTACAATCCAGCA	84708
rs74993616	snp	C/T	0.00755907	0.0610114	intron-variant	LNX1	GRCh38.p7	4:53492589	AGCTCATTCTCTCTG[C/T]TGTGCATAGAGTAGG	84708
rs74999992	snp	A/T	0.5	0	intron-variant	LNX1	GRCh38.p7	4:53561928	CGTGTATCCCAGAAT[A/T]AAAAAAAAGGAAAAA	84708
rs75004476	snp	A/C	0.00716266	0.059414	intron-variant	LNX1	GRCh38.p7	4:53547455	CAGCTAGAGGAGACT[A/C]TATAGGAACTGGGGT	84708
rs75016439	snp	A/G	0.0414363	0.137845	intron-variant	LNX1	GRCh38.p7	4:53496735	GATAAGGTAGGAAAA[A/G]GCAAAAGAAAAGCAT	84708
rs75016695	in-del	-/A	0.306927	0.243432	intron-variant	LNX1	GRCh38.p7	4:53631708	TGGATATATTTTTTT[-/A]ATGCCCTAGGTGATT	84708
rs75039427	snp	A/C	0.00398564	0.0444627	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53597680	TAGGAGGCTGCCATG[A/C]CTACATCTGCCCAGT	84708
rs75046089	snp	A/G	0.0138799	0.0821421	intron-variant	LNX1	GRCh38.p7	4:53586484	GCCTGTGACAAATGC[A/G]TCAAACACAAGAAGC	84708
rs75088166	snp	C/T	0.00318978	0.0398085	intron-variant	LNX1	GRCh38.p7	4:53488117	CTCTATAGCCTATAA[C/T]TCAATTTCCCTACAA	84708
rs75107561	snp	A/G	0.0166325	0.0896639	intron-variant	LNX1	GRCh38.p7	4:53482272	TAAAGAAAAAGAGAT[A/G]GAGTTAATGGCAGTA	84708
rs75114615	snp	C/G	0.0189856	0.0955633	intron-variant	LNX1	GRCh38.p7	4:53525675	TTTTGCACCAACCTA[C/G]TAACTTGAGGGTTCA	84708
rs75119916	snp	C/G	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53541797	GATTTACAAGTAAAA[C/G]AGGCAAACACTAAAA	84708
rs75188344	snp	C/T	0.105569	0.204058	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53522853	CTGTAATTCCACCCC[C/T]AGAGAAAACTGCTGC	84708
rs75195425	snp	A/G/T	0.00755907	0.0610114	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53595782	CCCATGAAGCTTGGC[A/G/T]TTCTCAAGGACTCCT	84708
rs75206406	snp	A/G	0.0125309	0.0781565	intron-variant	LNX1	GRCh38.p7	4:53557855	TAAACACACAGGCAC[A/G]GACAGAGAGGGGACT	84708
rs75313288	snp	A/G	0.029116	0.117091	intron-variant	LNX1	GRCh38.p7	4:53581157	GTATACTGGTCACCC[A/G]GGACCATGACAGTTG	84708
rs75319249	snp	C/T	0.0402882	0.136092	intron-variant	LNX1	GRCh38.p7	4:53614754	ATCTCCTCCTTGATG[C/T]CAACTGAATGCTTGC	84708
rs75320378	snp	A/T	0	0	intron-variant	LNX1	GRCh38.p7	4:53469972	TAGAAAAAGAGGGAA[A/T]CCTCCCTAACTCATT	84708
rs75358681	snp	A/G	0.00953873	0.0683987	intron-variant	LNX1	GRCh38.p7	4:53589733	CTTGAACCAATGGGT[A/G]GAGTTACCACAGGAA	84708
rs75361154	snp	G/T	0	0	intron-variant	LNX1	GRCh38.p7	4:53545820	TTTTTTTTTTTTTTT[G/T]TTTTTGAGACAGGGT	84708
rs75373223	snp	A/G	0.5	0	intron-variant	LNX1	GRCh38.p7	4:53490069	TCTCATTAAAAAAAA[A/G]GTTTGAAGAGCCTGT	84708
rs75398409	snp	A/T	0.5	0	intron-variant	LNX1	GRCh38.p7	4:53526116	CTAGAAAAGAAAAAA[A/T]ATTAAAAAAAGATAA	84708
rs75418012	snp	C/T	0.00358779	0.0422022	intron-variant	LNX1	GRCh38.p7	4:53586651	TACCATGCCAAGGAA[C/T]TTGGCTTTCTAGAGC	84708
rs75421795	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53553517	TTCATCTACAAGTCT[C/T]TCCACATGCAGGGCT	84708
rs75487561	snp	A/T	0.25045	0.25	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53596045	ACATTACATACCATC[A/T]TATTGGCCGTAATTA	84708
rs75490087	snp	A/C	0.0256215	0.110247	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53513580	TGTGTTACTAAATAG[A/C]TCCTTATCTGTCATT	84708
rs75492489	snp	C/T	0.00993419	0.0697739	intron-variant, nc-transcript-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53523020	GCTGAGCAACAGACC[C/T]ATTTGGGAAGATTTT	84708
rs75510082	snp	A/C	0.0448719	0.142907	intron-variant	LNX1	GRCh38.p7	4:53465986	AGTGACTTTAATTAA[A/C]TACTCTTTCAAAAAA	84708
rs75510187	snp	G/T	0.00119737	0.0244387	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53515226	ACATCACTTAAGGCC[G/T]CCAGTCAAGACACAT	84708
rs75514385	snp	C/T	0.0232847	0.105357	intron-variant	LNX1	GRCh38.p7	4:53583772	TCAGGGAATGCCTTT[C/T]ATAAGCAGGTTAGAG	84708
rs75557521	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53572046	AGCACAAATGTATAA[C/T]TGCAACACGGGACTG	84708
rs75570238	snp	A/T	0.5	0	intron-variant	LNX1	GRCh38.p7	4:53619169	ATTAGATGGCCTTAA[A/T]TTTTTTTACATTGAG	84708
rs75584279	snp	C/T	0	0	intron-variant	LNX1	GRCh38.p7	4:53469996	ACTCATTTCATGAGG[C/T]CAGCATCATCCCGAT	84708
rs75631830	snp	G/T	0.0482946	0.147699	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53593964	AAGAAAAGAGGGAAG[G/T]TTCTGATTTCATGCT	84708
rs75649001	snp	C/T			intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53575309	TTAAACAGTAGAATA[C/T]TACCACAATACATAT	84708
rs75681982	snp	A/T	0.5	0	intron-variant	LNX1	GRCh38.p7	4:53613348	CTGCTTTCCAGGAAT[A/T]TTTTTTTTTTAACTT	84708
rs75716340	snp	A/G	0.0023933	0.0345097	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507129	TTCTTCAATCTATGT[A/G]AAAAGATGATAATAC	84708
rs75718680	snp	C/T	0.0232847	0.105357	intron-variant	LNX1	GRCh38.p7	4:53643854	AAAGTTTGTTGGGGC[C/T]TAGCACATGGGAAGA	84708
rs75721555	snp	A/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519669	GTATCTGACACACAC[A/T]CACATGCGCGCACAT	84708
rs75789541	snp	A/G	0	0	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53594730	TTAATTTTTTTTTTT[A/G]GAGACAACTCTCCCT	84708
rs75822562	snp	G/T	0.5	0	missense, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461453	ATTCTTCCATCATTG[G/T]ATGCTGGTGTTCCTT	84708
rs75824785	snp	G/T	0.5	0	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53505278	AACTTTTTTTTTTTT[G/T]GAGATGGAGTCACCC	84708
rs75857635	snp	A/G	0.164219	0.234823	intron-variant	LNX1	GRCh38.p7	4:53635709	AAACAGGAAGAAACA[A/G]CCAAGAGATTGAAAA	84708
rs75893784	snp	A/T	0.0146672	0.084371	intron-variant	LNX1	GRCh38.p7	4:53647955	ATTTCCTTCCTTTTT[A/T]AGGCTGAATTTATCC	84708
rs75895214	snp	A/T	0.116138	0.211142	intron-variant	LNX1	GRCh38.p7	4:53547382	TGTGAGGTAAGTGTT[A/T]TTCCCATTTATAGGT	84708
rs75912591	snp	A/G	0.0611083	0.163768	intron-variant	LNX1	GRCh38.p7	4:53647528	TTTCTCAGAGAAGAA[A/G]TCTGCTATTTTCCCA	84708
rs75939404	snp	C/T	0.0154538	0.0865337	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53594122	GTAATCTGGTCTATA[C/T]GCTGAAAGTGTGTGT	84708
rs75939724	snp	G/T	0	0	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53502948	TCTTTTTTTTTTTTT[G/T]TAGATGGAATCTTGC	84708
rs75947364	snp	C/G	0.00438332	0.0466095	intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53559573	AGTGCTTAACTCAGA[C/G]TGCTAGTAAGAAGGT	84708
rs75958584	snp	A/G	0.0126979	0.078662	intron-variant	LNX1	GRCh38.p7	4:53644898	GGAAGTCTGGGTAAG[A/G]ATTACAAGTAGCACA	84708
rs75962210	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53622519	CTCACCCCAGGGCTA[A/G]CAATGGACCATTATC	84708
rs75994048	snp	C/T	0.0197687	0.0974348	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS2	GRCh38.p7	4:53591208	GGGAGAAGTTTATTG[C/T]GCAACTAGAATGTCA	84708
rs76027543	snp	C/T	0.0197687	0.0974348	intron-variant	LNX1	GRCh38.p7	4:53632422	CTGCCTTCTGCTAAA[C/T]AGCTGCTCCCTTGAG	84708
rs76034902	snp	C/G	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53637538	TACTTTTTCACAACT[C/G]TGTGAAGTTGTAGCA	84708
rs76067669	snp	A/T	0.00517822	0.0506191	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53518103	AGCTGGAAAGTCATG[A/T]GAAAATGCAGGCCAC	84708
rs76086045	snp	A/G	0.0948562	0.196037	intron-variant	LNX1	GRCh38.p7	4:53548085	GAAAGCTGGAAGGGC[A/G]TGGGGCCACATGAGC	84708
rs76096421	snp	C/T	0.0383715	0.133092	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53506170	CCTGATTTAAAATCT[C/T]GGTTCTGCCATTTTT	84708
rs76097839	snp	C/T	0.0368353	0.130617	intron-variant	LNX1	GRCh38.p7	4:53463479	AGTTGGGTCTGACTT[C/T]GTGGGCATTTTTTTC	84708
rs76150571	snp	A/G	0.00993419	0.0697739	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53605443	GTATGGGGGTGGGGG[A/G]TAAAGTACCTAAATA	84708
rs76163141	snp	A/G	0.5	0	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53502894	AATGCCTCTACACTC[A/G]TTCAAGTTTTATTAT	84708
rs76194249	snp	A/C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53580515	CTTGCAGCAATAGCA[A/C/T]ACACTACTGCTGTTA	84708
rs76235758	snp	C/G	0.0193772	0.0965046	intron-variant	LNX1	GRCh38.p7	4:53538495	TTTTGAATGCATGAG[C/G]GTTCATCGTTGAAAA	84708
rs76256022	snp	A/T	0.0659589	0.169201	intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53559159	AGAAAAGTCTACAGG[A/T]TGAGACGAGTTGCAA	84708
rs76289468	snp	A/G	0.5	0	intron-variant	LNX1	GRCh38.p7	4:53556100	CAATTAAGGATCTCA[A/G]GATAAGATTACCATG	84708
rs76305068	snp	C/T	0.0221141	0.102801	intron-variant	LNX1	GRCh38.p7	4:53492655	CAAAGAGGCTCCAGC[C/T]GTCACTCAGACCAGG	84708
rs76306873	snp	A/C	0.5	0	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507748	GACACTGCAGGAGTG[A/C]TGAATCATTAGGTCT	84708
rs76309111	snp	A/G	0.151001	0.229563	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519955	GCAAACCGATGTGCT[A/G]GTGCTCACCCTATAA	84708
rs76341726	snp	A/G	0.0193772	0.0965046	intron-variant	LNX1	GRCh38.p7	4:53628257	TGCATCCAACAAAGT[A/G]TTAGTATTCAGAATC	84708
rs76342881	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53641185	CTGCTTGGCCACTTT[C/G]TCTGTTCTGGGGAAG	84708
rs76358501	snp	A/G	0.00953873	0.0683987	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498413	TATAGAGACAGATAA[A/G]TATTTATATACAGAG	84708
rs76360996	snp	A/G	0.0158469	0.0875917	intron-variant	LNX1	GRCh38.p7	4:53633891	TCACCAGAAAAGCCC[A/G]ACAGTGAAATGTGTG	84708
rs76364435	snp	C/T	0.236144	0.249616	intron-variant	LNX1	GRCh38.p7	4:53588646	CTTCAGTTGTAAGGA[C/T]GGAGGGGGCCTGTGA	84708
rs76403530	snp	A/T	0.120326	0.21374	intron-variant	LNX1	GRCh38.p7	4:53552331	ACAGGCAAGAGCAGG[A/T]CACACCATCAGAATA	84708
rs76410339	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53645046	CCAGASAGCCAAAAG[A/T]TGATCCAGGTGATAA	84708
rs76412590	snp	A/T	0.5	0	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519667	AGGTATCTGACACAC[A/T]CACACATGCGCGCAC	84708
rs76413910	snp	C/T	0.00676609	0.0577691	intron-variant	LNX1	GRCh38.p7	4:53580625	TTACGAGTAAAAAGG[C/T]AGAAATGAAGAAGTT	84708
rs76453422	snp	C/T	0.00199481	0.0315187	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53594645	CTCCAGGCACACTAG[C/T]AGTTGGTTTTACCCC	84708
rs76466376	snp	C/T	0.277778	0.248452	intron-variant	LNX1	GRCh38.p7	4:53548834	ATATACCATGGAATA[C/T]TATGTAGTTATATAA	84708
rs76516048	snp	A/C	0.232943	0.249417	intron-variant	LNX1	GRCh38.p7	4:53590080	TGGTGGCCAAACCCC[A/C]CCCCTTAAACTCACA	84708
rs76535674	snp	G/T	0.299916	0.244966	intron-variant	LNX1	GRCh38.p7	4:53541572	GGGATCTATTCAGTT[G/T]TGTGTCAAATTCTTA	84708
rs76556809	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53479647	GACTTTTCTATCTAT[C/T]TTTTTTCGCCATTCT	84708
rs76577510	snp	A/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53623645	TGTAATTTTAGCCAA[A/T]CAAATTCTCAATTTG	84708
rs76604683	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53627861	TCTCCTTCTGCATGC[C/T]CCTTTGGGAGATTTG	84708
rs76656265	snp	A/C	0	0	intron-variant	LNX1	GRCh38.p7	4:53607127	GGATGCCCTTTATTT[A/C]TTTCTCTTGCCTGAT	84708
rs76659636	snp	A/C	0.00755907	0.0610114	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53520207	TCACAGCAACCCCTG[A/C]GGGTCCAAACCTTAT	84708
rs76667930	in-del	-/TGT			intron-variant	LNX1	GRCh38.p7	4:53534901	TCTTAACAGCCTTGT[-/TGT]AAAAATCGTTGAGTG	84708
rs76693459	snp	C/T	0.288127	0.247076	intron-variant	LNX1	GRCh38.p7	4:53466551	AGGCGTCGCCTCACC[C/T]GGGAAGCACAAGGGA	84708
rs76712257	snp	A/G	0.163892	0.234703	intron-variant	LNX1	GRCh38.p7	4:53642953	AATGGTTCTCTGTGT[A/G]GGGTGATTTTGCCCT	84708
rs76760155	snp	A/T			missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507335	CAGGGGCAGTGGTGT[A/T]TTCAGAATTTTCCCT	84708
rs76797593	snp	C/T	0.00755907	0.0610114	intron-variant	LNX1	GRCh38.p7	4:53557041	GCACACACAGCAACA[C/T]TTTTCATATGATTGC	84708
rs76817462	snp	C/T	0.0209421	0.100162	intron-variant	LNX1	GRCh38.p7	4:53614738	TATGGCTCACGAGTT[C/T]ATCTCCTCCTTGATG	84708
rs76855251	snp	A/G	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53625211	GCACAAACAGAAGAA[A/G]AAATAAATTGGTTTT	84708
rs76888878	snp	C/T	0.0383715	0.133092	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53506573	CAGGAATAGGAGTGG[C/T]GCCAGGTGCGGTGGC	84708
rs76902982	snp	C/T	0.0126979	0.078662	intron-variant	LNX1	GRCh38.p7	4:53634661	CTACTTACTACCTCT[C/T]ATGCAGGAAGGGTGG	84708
rs76912190	snp	C/T	0.00914312	0.0669923	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53597927	ATTTCTCACATTTGT[C/T]GAACCATTGCCTAGA	84708
rs76916145	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53491445	TTTTGAGATAAAAGG[C/T]AGGAATACATTCCAA	84708
rs76930004	snp	C/T	0.02016	0.0983543	intron-variant	LNX1	GRCh38.p7	4:53487732	TGCGACTGATAACTA[C/T]ATAAGCTGCTTATAG	84708
rs76940133	snp	C/T	0.0887219	0.191022	intron-variant	LNX1	GRCh38.p7	4:53545768	AGTGATGAGCCAGGA[C/T]TTGTACTCAGATTTG	84708
rs76984661	snp	A/C/T	0.0197687	0.0974348	intron-variant	LNX1	GRCh38.p7	4:53638592	ACTTAGTGCCCCGTT[A/C/T]TTCCTCATTTTTGTG	84708
rs76987071	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53515237	GGCCGCCAGTCAAGA[C/T]ACATCAGCTCTGCCT	84708
rs77005321	in-del	-/TT			intron-variant	LNX1	GRCh38.p7	4:53470035	AGTTTTCTTTTTTTT[-/TT]TGTTGTATCTCTGGT	84708
rs77006669	snp	A/C	0.5	0	intron-variant	LNX1	GRCh38.p7	4:53523828	ATCCTAAAATACTCA[A/C]TGAAGCCTCCATTCA	84708
rs77008304	snp	G/T	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53536976	TGGTGTTAACAGTGA[G/T]GATTTCTAATTACTT	84708
rs77015893	snp	C/T	0.00318978	0.0398085	intron-variant	LNX1	GRCh38.p7	4:53548119	CAGAAGGAGTGATGG[C/T]TGAAAAAAAAAAAAA	84708
rs77022810	snp	A/G	0.00478085	0.0486577	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53520050	TTTTCCTTTGTGGAT[A/G]TTCTGTCCCCACGTT	84708
rs77039857	snp	A/G	0.00874735	0.0655527	intron-variant	LNX1	GRCh38.p7	4:53491446	TTTGAGATAAAAGGC[A/G]GGAATACATTCCAAG	84708
rs77052286	snp	A/C			intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53575308	TTTAAACAGTAGAAT[A/C]CTACCACAATACATA	84708
rs77074224	snp	C/G	0.0517044	0.152246	intron-variant	LNX1	GRCh38.p7	4:53534947	CAATTACAACAGAAA[C/G]AAATGATTGCTCATG	84708
rs77091431	snp	A/C/T	0.00994088	0.0698686	intron-variant	LNX1	GRCh38.p7	4:53549151	AAACCTTGACATGTA[A/C/T]CCCCCAAATCTAAAA	84708
rs77100607	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53529141	CACACACACAAACAC[A/C]TGCACACACAGAAAA	84708
rs77169843	snp	A/T	0	0	intron-variant	LNX1	GRCh38.p7	4:53491286	GAGAAAAAAAAAAAA[A/T]ATCTTGCTAAGAATG	84708
rs77175813	snp	A/G	0.0655868	0.168795	intron-variant	LNX1	GRCh38.p7	4:53554178	TTCTGTCCAGCTCTC[A/G]CCATTGGACTATATG	84708
rs77178500	snp	A/G	0.0193772	0.0965046	intron-variant	LNX1	GRCh38.p7	4:53481585	AAATATGGGACTTTG[A/G]GCTTTTAGTTTTACA	84708
rs77190821	snp	A/G	0.0146672	0.084371	intron-variant	LNX1	GRCh38.p7	4:53586693	CTTTCAGATGGATAG[A/G]TGAAGAAGGGCAAAG	84708
rs77197241	snp	C/T	0.0111196	0.0737302	intron-variant	LNX1	GRCh38.p7	4:53640329	TAGAGAAGTCTTTCT[C/T]TGGGAGAGCATCCTT	84708
rs77208111	snp	C/T	0.0193772	0.0965046	intron-variant	LNX1	GRCh38.p7	4:53624734	ACCTTGACCTTTCTG[C/T]AGCATTTGGTCCTGC	84708
rs77287932	snp	C/T	0.162253	0.234095	intron-variant	LNX1	GRCh38.p7	4:53649466	CCAGGATTTGAACTC[C/T]GGAAGTCTGGCTCCA	84708
rs77358790	in-del	-/GTT	0.0111196	0.0737302	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53598722	GAGGGCTTACTCGTT[-/GTT]AAGTTACATCTTGAG	84708
rs77413219	snp	C/T	0.5	0	intron-variant	LNX1	GRCh38.p7	4:53617236	GAGAGCAAAGGAGTT[C/T]TGAGACCTCACCTTT	84708
rs77429364	snp	C/G	0.0448719	0.142907	intron-variant	LNX1	GRCh38.p7	4:53489989	CACAAAAGTTCTACC[C/G]TTTTTTGCAGGTATG	84708
rs77453629	snp	C/T	0.299916	0.244966	intron-variant	LNX1	GRCh38.p7	4:53542845	CCCGGTAAGAACCCC[C/T]CTCTCCCATCAGGAA	84708
rs77466171	snp	A/G	0.00676609	0.0577691	intron-variant, utr-variant-3-prime	LNX1, LOC101928879	GRCh38.p7	4:53577291	TCTAGGTCTTTTAAA[A/G]CTTCTCTGTAGTGTT	84708
rs77531402	snp	C/T	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53482015	CCATCTTGTAATTTG[C/T]CAAGAGCATGAGAGC	84708
rs77541461	snp	C/G	0.497933	0.032082	intron-variant	LNX1	GRCh38.p7	4:53470907	tatcatgaaaatggg[C/G]atactgcccaaggta	84708
rs77546058	snp	A/G	0.5	0	intron-variant	LNX1	GRCh38.p7	4:53548122	AAGGAGTGATGGTTG[A/G]AAAAAAAAAAAAGTC	84708
rs77617175	snp	A/G	0.0452528	0.143452	intron-variant	LNX1	GRCh38.p7	4:53492460	GCAGGCCATAGTAAC[A/G]ATCTGCAACTTTAAC	84708
rs77629803	snp	C/T	0.0166325	0.0896639	intron-variant	LNX1	GRCh38.p7	4:53647588	AAAAGCCAGGATTCA[C/T]TGGCATTTTTTACTT	84708
rs77649474	snp	A/T	0	0	intron-variant	LNX1	GRCh38.p7	4:53630307	TTGCTAAAATTTTTT[A/T]GTAACCCCCAGATCA	84708
rs77653635	snp	A/T			intron-variant, downstream-variant-500B, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460059	CTCTATGAAATAAAT[A/T]AATTAATTACCCATA	84708
rs77679303	snp	A/G	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53630050	AATCATGTTGAAAAC[A/G]TGAGTATTTTCCCAT	84708
rs77680450	snp	G/T	0	0	intron-variant	LNX1	GRCh38.p7	4:53544214	TCTCTCTTTTTTTTT[G/T]GAGACAGTCTCACTC	84708
rs77692430	snp	A/G	0.0236746	0.106192	intron-variant	LNX1	GRCh38.p7	4:53578348	TACACACACCTTCAC[A/G]GTATAGCTGACTATA	84708
rs77704934	snp	A/G	0.164873	0.23506	intron-variant	LNX1	GRCh38.p7	4:53646379	CCATTCTCAGTCTCT[A/G]TCCTCTAACTCTGCT	84708
rs77755110	snp	C/G	0.00478085	0.0486577	intron-variant	LNX1	GRCh38.p7	4:53529686	AGAGAGTCAGGAGGA[C/G]GTGTACAAGCTACCA	84708
rs77818307	snp	C/T	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53499811	AAGAAGAGGCCAAGG[C/T]CTAGTTGGTGGCCTT	84708
rs77839254	snp	C/T	0.00755907	0.0610114	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53518950	GTGAGTCTGTCATAA[C/T]GGGGTTGGCATCTTC	84708
rs77894545	snp	A/C/G	0.0213452	0.101169	intron-variant	LNX1	GRCh38.p7	4:53646940	TTGAAATGAACCTGT[A/C/G]TGTTTAGAAGTGGAG	84708
rs78002060	snp	A/C	0.444444	0.157135	intron-variant	LNX1	GRCh38.p7	4:53470025	ATACCGAAGCCGGGC[A/C]GAAACACAACCAAAA	84708
rs78024794	snp	C/T	0.0134861	0.0810011	intron-variant	LNX1	GRCh38.p7	4:53613141	TGGAGAATTTATATG[C/T]GTGGAAGAGAAGAGG	84708
rs78069778	snp	C/T	0.0799831	0.183287	intron-variant	LNX1	GRCh38.p7	4:53555220	ATTCCTGCTCCCAAG[C/T]GTGCTAAACTGGCCC	84708
rs78071344	in-del	-/TT			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53513114	CAACAATTTTTTTTT[-/TT]AACTCAAAAACCGCC	84708
rs78096209	snp	C/T	0.0146672	0.084371	intron-variant	LNX1	GRCh38.p7	4:53649654	ACACCACTCCCTTTA[C/T]TCCCCTTCTAGTCAG	84708
rs78152271	snp	G/T	0.163892	0.234703	intron-variant	LNX1	GRCh38.p7	4:53640086	TACATATACCAAGTA[G/T]ACAAAAGTATGCCTG	84708
rs78196802	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53495161	AAACAGTAACGAGAC[A/G]TGGGATCTCTCTGTA	84708
rs78216904	snp	A/C	0.0260105	0.111035	intron-variant	LNX1	GRCh38.p7	4:53617931	AGACCTCTTTTTTCC[A/C]TGGAAAGATAGATAT	84708
rs78220446	snp	A/T	0.0107246	0.0724382	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53596219	CTGGTTCTGTGTATA[A/T]GGAAGATATTCCATT	84708
rs78223142	in-del	-/C	0.117537	0.212022	intron-variant	LNX1	GRCh38.p7	4:53571331	GCGTAAATTAAGAAT[-/C]TTGAGATGAAGGAGC	84708
rs78236582	snp	A/T	0.5	0	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53605754	TTACAAATGGCAGTA[A/T]CTCCTTCTTTAAGGC	84708
rs78249784	snp	C/T	0.0260105	0.111035	intron-variant	LNX1	GRCh38.p7	4:53562952	ACAATGGCTCAAGCC[C/T]GTAATCCCAGAACTT	84708
rs78285727	snp	A/G	0.00755907	0.0610114	intron-variant	LNX1	GRCh38.p7	4:53555595	GAGGTACCATGCCTC[A/G]ATTCTTATTGCCTGG	84708
rs78291969	snp	C/G	0.0225045	0.103662	intron-variant	LNX1	GRCh38.p7	4:53483429	CACATGTGTCAGGTA[C/G]TATGGGCCATTATTC	84708
rs78309209	snp	C/T	0.0429648	0.14013	intron-variant	LNX1	GRCh38.p7	4:53483020	TCCACTCCACATCAT[C/T]GATATGGTTTGACTG	84708
rs78313591	snp	C/T	0.0209421	0.100162	intron-variant	LNX1	GRCh38.p7	4:53615335	AGTATTTCTTACTCC[C/T]GTGAATCTACCTGGG	84708
rs78314539	snp	G/T	0.0325976	0.123435	intron-variant	LNX1	GRCh38.p7	4:53588721	AACTGACATGCAGGG[G/T]GGTTGAGGTTCTCCC	84708
rs78315295	snp	C/G	0.0123036	0.0774623	intron-variant	LNX1	GRCh38.p7	4:53642818	ATGAGAGGGGTCGCT[C/G]CACTTGAAGAATCCC	84708
rs78375877	snp	A/G	0.5	0	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53500516	TTGTGAGCATTTTCA[A/G]AACCCGTGACCTTAG	84708
rs78398268	snp	C/T	0.0807149	0.183963	intron-variant	LNX1	GRCh38.p7	4:53590239	CAAAAATGATCTCAG[C/T]TTGTTTCAATTCATA	84708
rs78433571	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53543755	CTGGGCTCCTTTGAG[A/G]TCCATATGCCTCAAT	84708
rs78462855	snp	A/T	0	0	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53502947	ATCTTTTTTTTTTTT[A/T]TTAGATGGAATCTTG	84708
rs78468739	snp	C/T	0.0588605	0.161139	intron-variant	LNX1	GRCh38.p7	4:53557339	ATGGAAATATGGGTG[C/T]TCAAGGCATGTTTCT	84708
rs78472635	snp	A/T	0.0479149	0.147179	intron-variant	LNX1	GRCh38.p7	4:53611881	GCCAAAAGCTCTGAG[A/T]GTAAAGATAGCTGTA	84708
rs78487283	snp	C/T	0.00953873	0.0683987	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53602952	AGACCACTTTTGAAG[C/T]TAGAAAAGGCAAGGA	84708
rs78519493	snp	C/T	0.0142736	0.0832652	intron-variant	LNX1	GRCh38.p7	4:53572028	AAATGAACACAGCTC[C/T]CCAGCACAAATGTAT	84708
rs78561336	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519832	CAAAGATTCACTTGC[A/G]CAGGTTTGCGCAGTT	84708
rs78635711	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53553017	AAACCAACCAGGGTC[C/T]TCTTTATCACAGCTT	84708
rs78679231	in-del	-/G	0.25801	0.249872	intron-variant	LNX1	GRCh38.p7	4:53606207	TAATAAAGAAAAAAA[-/G]GGAGAAGTTCCAAAT	84708
rs78716877	snp	C/T	0.249038	0.249998	intron-variant	LNX1	GRCh38.p7	4:53552934	TCAAGTACAGTGCTG[C/T]ATCCTGAAACATCTG	84708
rs78738977	in-del	-/AA			intron-variant	LNX1	GRCh38.p7	4:53466165	TTTTAAGAAAAAAAA[-/AA]TCACATATTATTTGG	84708
rs78777611	snp	A/T	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53583362	GTGTCTGTGTGTGCA[A/T]GATGGGGGGCAAATA	84708
rs78800179	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53490954	CTGCTTATAAAGCAC[A/G]TTGGCTTTGTTTAGT	84708
rs78829667	snp	C/T	0.0372196	0.131242	intron-variant	LNX1	GRCh38.p7	4:53563289	TCAAGCAAACCAATG[C/T]AAAATTTATAAACAA	84708
rs78861026	snp	C/T	0.00517822	0.0506191	intron-variant	LNX1	GRCh38.p7	4:53479039	AATGGAGGAAGGAAC[C/T]GATTACAGACCATTA	84708
rs78887947	snp	A/T	0.0197687	0.0974348	intron-variant	LNX1	GRCh38.p7	4:53463471	CCTTGGTTAGTTGGG[A/T]CTGACTTTGTGGGCA	84708
rs78893305	snp	A/G	0.0197687	0.0974348	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53597153	AGCCTGGAGATGAGT[A/G]CCTCTACCTATGTAT	84708
rs78896495	snp	C/G	0.0146672	0.084371	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53513133	CTCAAAAACCGCCCA[C/G]GGAAATGTTCCCATC	84708
rs78897156	snp	A/G	0.0410537	0.137264	intron-variant	LNX1	GRCh38.p7	4:53530259	AATCGTAAGTAAAAA[A/G]GCCTAATGATAATAG	84708
rs78905594	snp	A/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53512377	TCTAATCTCTGGTAA[A/T]TAAAAAAAACTGCCA	84708
rs78907433	snp	G/T	0.0158469	0.0875917	intron-variant	LNX1, LOC101928879	GRCh38.p7	4:53575574	CAAACTAGGGCTCTG[G/T]GTCAACTTTCATGGT	84708
rs78928406	snp	C/T	0.0142736	0.0832652	intron-variant	LNX1	GRCh38.p7	4:53552088	TAGTGATTCCACTTA[C/T]AAACCAAAAATATTT	84708
rs78933713	snp	A/G	0.0205511	0.0992634	upstream-variant-2KB	LNX1	GRCh38.p7	4:53654435	TTTCCATTCAGAAAG[A/G]TAAGGTAGGTGGGGA	84708
rs78938969	snp	A/G	0.00676609	0.0577691	intron-variant	LNX1	GRCh38.p7	4:53613715	GTCTATGATTGATGG[A/G]TATTTAGGTTGATTC	84708
rs78939933	snp	A/C	0.0236746	0.106192	intron-variant	LNX1	GRCh38.p7	4:53584428	GAGAATACATAATAC[A/C]TGGCAATGTGTATAA	84708
rs78940916	snp	C/T	0.444444	0.157135	intron-variant	LNX1	GRCh38.p7	4:53589263	GCCAGCCAGCAACTC[C/T]TAAAAGCTTTGCCTG	84708
rs78952313	snp	G/T	0.0236746	0.106192	nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53604167	AAGTTGCCAAACTGC[G/T]GATTTTTGTTCTACC	84708
rs78961005	snp	G/T	0.5	0	intron-variant	LNX1	GRCh38.p7	4:53490445	TAGCTACATAAATCA[G/T]CAGCACCATATTTGA	84708
rs78973334	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53640143	GAATGACAGTGGTGG[G/T]GGGAGTATAGGTTTT	84708
rs78973935	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53543939	TAAAAACACCACCAC[A/G]GTAAACAAACAGAAA	84708
rs78979693	snp	C/T	0.0170251	0.090679	intron-variant	LNX1	GRCh38.p7	4:53617337	TTTTGAAGGTCACAG[C/T]AGTAAAAGATGGTTC	84708
rs78980142	snp	A/G	0.0236746	0.106192	nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53604690	CAAAAATGAATTATG[A/G]ATATCAGTCCAAAGT	84708
rs78982775	snp	A/G	0.00716266	0.059414	intron-variant	LNX1	GRCh38.p7	4:53619985	AAAAATGCAACAGCA[A/G]TTTTAATATTCTTAT	84708
rs78986674	in-del	-/A	0.212122	0.247114	intron-variant	LNX1	GRCh38.p7	4:53472794	ATATAGAGGCCAAGC[-/A]GGGGGAAGGCTGATA	84708
rs78988521	snp	A/G	0.0325976	0.123435	intron-variant	LNX1	GRCh38.p7	4:53587362	TGGGGATAGTTAATG[A/G]TTAAATCATATTAAC	84708
rs78996218	snp	A/G	0.02016	0.0983543	intron-variant	LNX1	GRCh38.p7	4:53648714	CCAACAATGGGGGCT[A/G]AAAGGCCACTGGAGA	84708
rs79028487	snp	C/T	0.0119091	0.0762411	intron-variant	LNX1	GRCh38.p7	4:53621018	CATGGCTTTCAAACA[C/T]TTTATTAACTGGCTT	84708
rs79047286	snp	A/T	0.24932	0.249999	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53597475	ATTTCCATAGAGAAC[A/T]GGTTTTCTAAGCACA	84708
rs79056134	snp	C/T	0.234401	0.249513	intron-variant	LNX1	GRCh38.p7	4:53590085	GCCAAACCCCCCCCC[C/T]TAAACTCACAAGCTT	84708
rs79066530	snp	C/T	0.0349115	0.127424	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53518805	TTTGGGGGGCAACTG[C/T]AACATGGGACGTAGG	84708
rs79117883	snp	A/G	0.0150606	0.0854603	intron-variant	LNX1	GRCh38.p7	4:53649442	ATCAACAAATCTTAG[A/G]TCACAGAACCAGGAT	84708
rs79162003	snp	A/C	0.214239	0.247429	intron-variant	LNX1	GRCh38.p7	4:53647859	TAAGTGGAATTATAT[A/C]GTATTTGTCCTTCTG	84708
rs79177594	snp	A/T	0.5	0	intron-variant	LNX1	GRCh38.p7	4:53540226	GTCTCTAAAAAAAAA[A/T]ACAAAAATTAGCCAG	84708
rs79182667	snp	A/T	0.00795532	0.062565	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53595458	TCTTGGGCATGGGGT[A/T]ATTTCTTATGCATGA	84708
rs79214165	snp	C/G	0.5	0	intron-variant	LNX1	GRCh38.p7	4:53491985	AGAGATAGGATTTCA[C/G]CCTGTTGACCAGGCT	84708
rs79262058	snp	C/T	0.0252325	0.109451	intron-variant	LNX1	GRCh38.p7	4:53539049	AAAGTGAAGTCAGTT[C/T]CAAGGGCTGAATGTG	84708
rs79264616	snp	G/T	0.00835141	0.0640778	intron-variant	LNX1	GRCh38.p7	4:53549954	TGGCATCTTGAAACT[G/T]CTGGGTTTTGTTTAG	84708
rs79272461	snp	A/C	0.0111196	0.0737302	intron-variant	LNX1	GRCh38.p7	4:53527441	ATGAATTCCCCCACA[A/C]CCATAATTAGTCTCT	84708
rs79272978	snp	A/G	0.187369	0.242028	intron-variant	LNX1	GRCh38.p7	4:53623187	CCTGAGGATGAGAGC[A/G]TTTGCGTTGAGAGCA	84708
rs79282990	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53475617	CCTATGCTAGTATAT[C/G]TTCAGTGATGCTAAT	84708
rs79315933	snp	C/T	0.00755907	0.0610114	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53521364	ACATTTCCTCCGTTC[C/T]TCAAAGTGCATTCCA	84708
rs79318302	snp	G/T	0.5	0	intron-variant	LNX1	GRCh38.p7	4:53491816	GTTTGTTTGTTTTTT[G/T]AGAAAAGTTTCACTC	84708
rs79318513	snp	C/T	0.0329836	0.124112	intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53574284	GCCTCTGTTTTTCCA[C/T]GCATGCCAGTGGGAA	84708
rs79321696	in-del	-/AA			intron-variant	LNX1	GRCh38.p7	4:53527046	TTAGACTCTTCCCTG[-/AA]CCCCTAAAAAAAAAA	84708
rs79324622	snp	A/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53594030	CCCATTATTCAGAAG[A/G]AGAAGTAGAAACCTG	84708
rs79325125	snp	C/G	0	0	intron-variant	LNX1	GRCh38.p7	4:53548827	AAATGTGGTAGTCCA[C/G]GGAATACTATGCAGC	84708
rs79327109	snp	C/T	0.00478085	0.0486577	intron-variant	LNX1	GRCh38.p7	4:53630943	ATGGGAACCATCCAC[C/T]AGGGTGGATCAGGGC	84708
rs79393640	snp	C/T	0.0228947	0.104514	intron-variant	LNX1	GRCh38.p7	4:53529336	GGGACGGCAGCATAG[C/T]TGAGGAGACAAGGTA	84708
rs79406103	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53478270	TTAGAATGAATGGAA[C/T]TACATTATGCCATTT	84708
rs79419627	snp	A/G	0.0142736	0.0832652	intron-variant	LNX1	GRCh38.p7	4:53553076	AGGCAAATTCATTCA[A/G]TTTGGTTTAACTTAA	84708
rs79424028	snp	A/G	0.5	0	intron-variant	LNX1	GRCh38.p7	4:53548121	GAAGGAGTGATGGTT[A/G]AAAAAAAAAAAAAGT	84708
rs79437553	snp	C/T	0.02016	0.0983543	intron-variant	LNX1	GRCh38.p7	4:53556328	CCCCTATAGCCTTCA[C/T]AGGGAGCATGACCTT	84708
rs79442539	snp	G/T	0.0240643	0.107019	intron-variant, utr-variant-3-prime	LNX1, LOC101928879	GRCh38.p7	4:53577413	ACTGAAAATACAACT[G/T]CATGTTTCTGGGCCA	84708
rs79454278	snp	C/G	0.00755907	0.0610114	intron-variant	LNX1	GRCh38.p7	4:53580655	TTTTAAAAACAAAAG[C/G]AATGGCTATGAATGA	84708
rs79460906	snp	A/G	0.5	0	intron-variant	LNX1	GRCh38.p7	4:53491276	TTTTCAAAGTGAGAA[A/G]AAAAAAAAAAATCTT	84708
rs79475771	snp	A/G	0.0146672	0.084371	intron-variant	LNX1	GRCh38.p7	4:53643445	CTGAGACACCATCCC[A/G]GTCAAGAAACCTTGG	84708
rs79479868	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	LNX1, LOC101928879	GRCh38.p7	4:53577892	TTGTTTTGTTTTTGA[C/T]GATTTGATGTTTGGG	84708
rs79503218	snp	A/G	0.0193772	0.0965046	intron-variant	LNX1	GRCh38.p7	4:53626209	ATGCAGATAGAAAAT[A/G]TGTTCGTTTTCAAGG	84708
rs79542175	snp	A/G	0.0158469	0.0875917	intron-variant	LNX1	GRCh38.p7	4:53650295	GGAGGACATACGGTA[A/G]CTCCAGAATTCCAGG	84708
rs79543133	snp	A/G	0.117537	0.212022	intron-variant	LNX1	GRCh38.p7	4:53572598	GGAACCAGGATAAAC[A/G]ACATCTTCCAAATTT	84708
rs79586549	in-del	-/AAA			intron-variant	LNX1	GRCh38.p7	4:53491285	TGAGAAAAAAAAAAA[-/AAA]TCTTGCTAAGAATGC	84708
rs79588563	in-del	-/T	0.162253	0.234095	intron-variant	LNX1	GRCh38.p7	4:53541478	CACATTTCATATATA[-/T]TTTTTTTTCTAAAAG	84708
rs79623906	snp	C/T			synonymous-codon, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507336	AGGGGCAGTGGTGTT[C/T]TCAGAATTTTCCCTG	84708
rs79625021	snp	C/T	0.164873	0.23506	intron-variant	LNX1	GRCh38.p7	4:53646003	AATTGCTTTATTTAT[C/T]CCTTTCTGAAAAATG	84708
rs79626532	snp	C/T	0.00597247	0.0543191	intron-variant	LNX1	GRCh38.p7	4:53528126	CTAATCCTTTGTGTC[C/T]GCTCAGCGTATTTTC	84708
rs79669082	snp	A/G	0.0107246	0.0724382	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53598782	AGCCTGAACACTTTG[A/G]GAAGGGAGCTAACTT	84708
rs79676281	snp	A/G	0.0524604	0.153226	intron-variant	LNX1, LOC101928879	GRCh38.p7	4:53575430	AAATAGTTTTCAAGC[A/G]CCAACTCTGAGCTAG	84708
rs79687623	snp	C/T	0.0433465	0.140692	intron-variant	LNX1	GRCh38.p7	4:53465018	CAAATTTATCACCTA[C/T]TTGATAATTGTTATC	84708
rs79706781	snp	C/T	0.0310518	0.120672	intron-variant	LNX1	GRCh38.p7	4:53464088	AAAGACGACAGTGGA[C/T]GTAGGATGTTTTGAG	84708
rs79707195	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53588158	TTTCAATTATTCCTC[C/T]CAACAGCTCTGAGTC	84708
rs79741309	snp	C/T	0.5	0	intron-variant	LNX1	GRCh38.p7	4:53470126	AATCCAGCAGCACAT[C/T]AAAAAGCTTATCTAC	84708
rs79784874	snp	A/T	0.215446	0.2476	intron-variant	LNX1	GRCh38.p7	4:53648346	TGGTTTTTGATTTGC[A/T]TTTTCCTAACCATTA	84708
rs79836019	snp	G/T	0	0	intron-variant	LNX1	GRCh38.p7	4:53572801	GGTGTGTGTGTGTGT[G/T]GGTGTGTGTGTGCAC	84708
rs79897439	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53526109	GCACTTTCTAGAAAA[A/G]AAAAAATATTAAAAA	84708
rs79905052	snp	C/T	0	0	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53511342	AGAAGCGGGGAAGAG[C/T]TGATTAGCATTGGCC	84708
rs79909585	snp	A/G	0.145305	0.227022	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53520496	CTTTGGGGTCACCGA[A/G]TTCATTTCCTCCATA	84708
rs79936534	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53553018	AACCAACCAGGGTCT[C/T]CTTTATCACAGCTTG	84708
rs79967236	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53543537	AAAGAARRAAAAAAA[A/T]TCACACTATACAAAG	84708
rs79974771	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53555443	CAATTTCACCAACAT[A/G]GACAATCTCTACCTC	84708
rs80031012	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53616724	CTTATCAATATGCCA[G/T]TCACTTTAATTAATT	84708
rs80087458	snp	C/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53571723	GCTGGAGTGCAGTAG[C/G]GCATCACAGCTCACT	84708
rs80104178	snp	A/G	0.0372196	0.131242	intron-variant	LNX1	GRCh38.p7	4:53572874	GCTTGGAAGACAAAA[A/G]TTTCCTAAATTTCTC	84708
rs80134958	snp	C/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	LNX1, FIP1L1	GRCh38.p7	4:53462957	GTACAAAGCAGGTAA[C/G]TGGCTATTCTGTAAA	84708
rs80136106	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53613521	CCTCCACCCCCCACC[A/G]TCCAGTAAGCCCCAG	84708
rs80241864	snp	C/T	0.00795532	0.062565	intron-variant	LNX1	GRCh38.p7	4:53590213	GGTGAGGAACGACTG[C/T]CTGTCTAAGGCAAAA	84708
rs80274042	snp	A/G	0.0146672	0.084371	intron-variant	LNX1	GRCh38.p7	4:53531023	TACAAAAAATTAGCC[A/G]GTGTGGTGGTGTGTG	84708
rs80279096	snp	A/G	0.0448719	0.142907	intron-variant	LNX1	GRCh38.p7	4:53490948	TTTTTCCTGCTTATA[A/G]AGCACGTTGGCTTTG	84708
rs80287776	snp	A/T	0.0178098	0.0926698	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53511630	GGTAAATCTGTCTTA[A/T]TATAAGAATGTTAAT	84708
rs80297174	snp	A/T	0.0150606	0.0854603	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53500062	AAGTGAGGAGGTTTA[A/T]GGCTGAGAGAAGGGG	84708
rs80298161	snp	A/C	0.0154538	0.0865337	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53593957	CACTGGAAAGAAAAG[A/C]GGGAAGGTTCTGATT	84708
rs80301484	snp	A/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53513105	TAACCATACCAACAA[A/T]TTTTTTTTTTAACTC	84708
rs80306563	snp	A/C	0.287867	0.247116	intron-variant	LNX1	GRCh38.p7	4:53472239	AACTATTGCAAGGAC[A/C]AAAAACCAAATACTG	84708
rs80327624	snp	C/G	0.0189856	0.0955633	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53595519	AGGATATGCCATTTC[C/G]GCAACCACATGATCT	84708
rs80339093	snp	C/T	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53588746	TCTCCCTTAGGGCTC[C/T]GTAGGCAAGCTAGTA	84708
rs80356119	snp	C/G	0.00953873	0.0683987	intron-variant	LNX1	GRCh38.p7	4:53611730	ATTTTATTGCACACT[C/G]AAGGATACGCTACAA	84708
rs111246396	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53596054	ACCATCATATTGGCC[A/G]TAATTACTTTTTTAA	84708
rs111253710	snp	A/G	0.00914312	0.0669923	intron-variant	LNX1	GRCh38.p7	4:53622858	TTGGAAATCTGACCT[A/G]TGTAACTGGAAGCCA	84708
rs111254217	snp	C/T	0.0345262	0.126772	intron-variant	LNX1	GRCh38.p7	4:53616971	CATAAGCTACAATCG[C/T]CAAAGCTTTTAAATA	84708
rs111261370	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53570521	GACTGTTGTGGGGTG[G/T]GGGGAGGGGGGAGGG	84708
rs111277471	snp	C/T	0.000428301	0.0146276	synonymous-codon	LNX1	GRCh38.p7	4:53496263	GGGTCTGTAGGCATC[C/T]GGGGCCTGTCCATTG	84708
rs111301664	snp	C/T	0.0298908	0.118541	intron-variant	LNX1	GRCh38.p7	4:53553391	CCCCTCTCCCAAAGA[C/T]TTTCATTTTAGTAGG	84708
rs111317353	snp	C/T	0	0	intron-variant	LNX1	GRCh38.p7	4:53541432	TTTTGGAAGATGACA[C/T]ACTTGGTAGTTTCTA	84708
rs111392206	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53579380	GATTTTTAGAGATAT[A/G]TGGAGCCAAAACCCC	84708
rs111395826	snp	C/T	0	0	intron-variant	LNX1	GRCh38.p7	4:53560669	ACTTGTACATAACAC[C/T]GAAGCATGCAGCCAT	84708
rs111404799	snp	C/G	0.00795532	0.062565	intron-variant	LNX1	GRCh38.p7	4:53583711	GGGAAGTGGTTAAGC[C/G]AAAAGAGTCCCAAGT	84708
rs111441827	in-del	-/TATTT	0.347694	0.230122	intron-variant	LNX1	GRCh38.p7	4:53535547	TAGATTTTATCATTC[-/TATTT]TGTTAGTGAATACTT	84708
rs111479919	snp	A/G	0	0	intron-variant	LNX1	GRCh38.p7	4:53529628	GAACAGAGCAAGCAC[A/G]GCATCTGACAGCTCC	84708
rs111483194	snp	A/G	0.00636936	0.0560724	intron-variant	LNX1	GRCh38.p7	4:53536993	ATTTCTAATTACTTA[A/G]GAAAATCTACCTTTT	84708
rs111507989	snp	C/T	0.021333	0.101051	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53594906	TTCTAGAGATGAGGT[C/T]TCACTATGGTGCCCA	84708
rs111558394	snp	A/G	0	0	intron-variant	LNX1	GRCh38.p7	4:53494136	CATGTGTTGTGGGAG[A/G]GACCCAGTGGGAGAT	84708
rs111560695	snp	C/T	1.66829e-05	0.00288811	intron-variant	LNX1	GRCh38.p7	4:53478766	ACAGATGGAAAAACA[C/T]GGCACATGAATTCAC	84708
rs111591248	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53535259	TAAACCATGGAGACC[A/G]GGCTTTGTTGTTTTG	84708
rs111591286	snp	C/T	0.184838	0.241358	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53600833	GCTCCTGGGTTCAAG[C/T]GATTTTCCTGCCTCA	84708
rs111593614	snp	C/G	0.00914312	0.0669923	intron-variant	LNX1	GRCh38.p7	4:53562992	GAGACGGATCACGAG[C/G]TCAGGAGATCGAGAC	84708
rs111613842	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53483333	AAATGACCCATTCTC[A/G]GGTATGTCTTTAATA	84708
rs111714552	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53608659	CACAAAGACATGCAC[A/G]TGTATGTTAATTGCA	84708
rs111763058	snp	A/G	0.5	0	intron-variant	LNX1	GRCh38.p7	4:53561937	CAGAATTAAAAAAAA[A/G]GAAAAAGGAGAGAAA	84708
rs111775227	snp	A/G	0.00874735	0.0655527	intron-variant	LNX1	GRCh38.p7	4:53587995	TCTTTGGCCCTCAAC[A/G]TACTACCGTTTCCAT	84708
rs111803323	snp	A/C	0.0391387	0.134304	intron-variant	LNX1	GRCh38.p7	4:53564937	AATACTGCGCTTTTC[A/C]GACGGGCTTAAAAAA	84708
rs111821977	snp	C/G	0.00914312	0.0669923	intron-variant	LNX1	GRCh38.p7	4:53623965	AAAGATCTGTATAAG[C/G]GTAGTTATTCCTCAA	84708
rs111890036	snp	A/G	0.0244538	0.107838	intron-variant	LNX1	GRCh38.p7	4:53494856	TGAAACGTCGCTGAG[A/G]CACAAAACTATCAGA	84708
rs111903043	snp	A/G	0.5	0	intron-variant	LNX1	GRCh38.p7	4:53482025	ATTTGCCAAGAGCAT[A/G]AGAGCTCTTTCCTTT	84708
rs111915634	snp	C/T	0.0146672	0.084371	utr-variant-5-prime, upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53591470	AACCGAGCAGCTCCT[C/T]GGGCCGCCGGAGTTG	84708
rs111919468	snp	G/T	0	0	intron-variant	LNX1	GRCh38.p7	4:53552555	ATATTTAGGCTAGGC[G/T]CAGTGGCTCACGCCT	84708
rs111944599	snp	A/T	0.00914312	0.0669923	intron-variant	LNX1	GRCh38.p7	4:53621942	GTAGGTCTCCCCCAC[A/T]ACCCACCCCACCACC	84708
rs111968738	snp	C/T	0.0138799	0.0821421	intron-variant	LNX1	GRCh38.p7	4:53481549	CTTGGATGGGAGACA[C/T]CTGTTATCTCTCCAA	84708
rs111980455	snp	A/G	0.0205511	0.0992634	intron-variant	LNX1	GRCh38.p7	4:53652132	TTTTTTAAATTGTAT[A/G]AGATTCTACCTGGTG	84708
rs111984928	snp	A/G	0	0	intron-variant	LNX1	GRCh38.p7	4:53487190	GCATTTTGCAGAGCT[A/G]TACACTGGAGCACAG	84708
rs112051361	snp	A/C	0.0150606	0.0854603	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53512920	TGGGCTCTCCCTGAG[A/C]ACTCGGGTGAGTTTG	84708
rs112150726	snp	A/G	0.0248432	0.108648	intron-variant	LNX1	GRCh38.p7	4:53536667	TACTGATGTGACACA[A/G]CTTCCTCAAATGAAT	84708
rs112154837	snp	C/G	0.0166325	0.0896639	intron-variant	LNX1	GRCh38.p7	4:53464325	GGATCAGGTACCTCT[C/G]AGTCTGTGGTGAAGG	84708
rs112175623	snp	A/G	0	0	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53595975	GTCATCTCTACAAAA[A/G]CCTCTTTGGCTATCT	84708
rs112177733	snp	A/G	0.00636936	0.0560724	intron-variant	LNX1	GRCh38.p7	4:53538902	GTTCTGTAACTTCTG[A/G]AAGTAATCACAGGGA	84708
rs112196083	snp	A/G	0.00597247	0.0543191	intron-variant	LNX1	GRCh38.p7	4:53627961	ACTTCACAAGTCTCT[A/G]AGGAAAAAAGTGCAT	84708
rs112215225	snp	A/G	0.5	0	intron-variant	LNX1	GRCh38.p7	4:53623676	AAGTTATATGGCTAT[A/G]TTTTATTTTTGTTAA	84708
rs112287804	snp	A/C	0.5	0	intron-variant	LNX1	GRCh38.p7	4:53536524	ACACTGTGTTCTACA[A/C]AAGCACATTACAAAA	84708
rs112288461	in-del	-/AT	0.0221141	0.102801	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53593747	GAAAAAAATGTAATC[-/AT]AAAAATGAACATTGT	84708
rs112288640	snp	A/G	0.00914312	0.0669923	intron-variant	LNX1	GRCh38.p7	4:53628418	AATCATCAGAGAAAT[A/G]CAAATTAAAACCATG	84708
rs112295046	snp	C/T	0.000576412	0.0169668	missense	LNX1	GRCh38.p7	4:53496165	ATGAAAACCCCAGGC[C/T]CATCCACCTTGCGCA	84708
rs112296992	snp	C/T	0.021333	0.101051	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53596121	ATGTGCTTAGCATAA[C/T]GCAGATGAGCAGATC	84708
rs112310703	in-del	-/C	0.5	0	intron-variant	LNX1	GRCh38.p7	4:53472700	CAAAAAAAAAAAAAA[-/C]AAAAAACAATGGGGA	84708
rs112316503	snp	A/C	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53627398	GTAAACTGATTCTAA[A/C]AGGGTTGAGCAATCT	84708
rs112354089	snp	A/G	0.0418186	0.138422	intron-variant	LNX1	GRCh38.p7	4:53538962	CACAGACAGTCTTCC[A/G]TGGCCAAGTCCAGGA	84708
rs112354403	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53569078	ATATCGTGAAAATGG[C/T]CATACTGCCCAAGGT	84708
rs112367602	snp	C/T	0.00953873	0.0683987	intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53560092	AGAAGTGACATGTTA[C/T]AGTCTTATCCTAAAT	84708
rs112411912	snp	C/G	0.00676609	0.0577691	intron-variant	LNX1	GRCh38.p7	4:53647107	GCTTCATCTGACAGA[C/G]GCTGTGACCTCTAAT	84708
rs112423717	snp	A/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53527127	CATTAGTTACAACTG[A/T]AATATACTATTGGGA	84708
rs112441328	snp	A/G	0	0	intron-variant	LNX1	GRCh38.p7	4:53527917	AAAATGCCACCAGCA[A/G]TTAGGTGATGTTTAT	84708
rs112445879	snp	C/G	0.00755907	0.0610114	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53522657	ATTCATGAAATACTT[C/G]TTTACTTTTATTAGG	84708
rs112458093	snp	C/T	0.0221141	0.102801	intron-variant	LNX1	GRCh38.p7	4:53584556	CCTTGGGAAGGATCA[C/T]GAATGATAAATGCGA	84708
rs112482437	snp	A/G	0.0310518	0.120672	intron-variant	LNX1	GRCh38.p7	4:53650066	AGCCCACATCCATAT[A/G]GATGAGCAGACCGAG	84708
rs112494387	in-del	-/CAGT	0.477853	0.102875	intron-variant	LNX1	GRCh38.p7	4:53616721	ACCTTATCAATATGC[-/CAGT]CATTCACTTTAATTA	84708
rs112500114	in-del	-/TCTA	0.49681	0.0398085	intron-variant	LNX1	GRCh38.p7	4:53479638	GAAAGAGATGACTTT[-/TCTA]TCTATCTTTTTTCGC	84708
rs112550826	snp	A/G	0.0126979	0.078662	intron-variant	LNX1	GRCh38.p7	4:53562770	TTACTAAGTGAGTAC[A/G]TTTTAAGTGTTTTCA	84708
rs112562784	snp	C/T	0	0	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53600448	TCCCAGGAACTTTTG[C/T]TTCCAAGAAAGGGCA	84708
rs112575086	snp	C/T	0.117537	0.212022	intron-variant	LNX1	GRCh38.p7	4:53563723	AATTTTTGGTAGAGA[C/T]GGGGTTTCACCATTT	84708
rs112590417	snp	A/G	0.5	0	utr-variant-5-prime	LNX1	GRCh38.p7	4:53652333	CACCTTTGTACGTGC[A/G]GGGGTTAACCTGGGC	84708
rs112603708	in-del	-/A	0	0	intron-variant	LNX1	GRCh38.p7	4:53470235	TAATCCAGCAAAGAC[-/A]AAAACCACATGATTA	84708
rs112613152	snp	C/G	0.5	0	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53512304	AAAATCTTAAAAACA[C/G]TGTGTGGTCCAAACA	84708
rs112618641	snp	A/G	0	0	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53515053	CTGTGACTCAAGGAT[A/G]TTTCACAGAGAGATG	84708
rs112637802	snp	C/T	0.0244538	0.107838	intron-variant	LNX1	GRCh38.p7	4:53580639	GTAGAAATGAAGAAG[C/T]TTTTAAAAACAAAAG	84708
rs112637890	snp	A/G	0.00636936	0.0560724	intron-variant	LNX1	GRCh38.p7	4:53536627	TTCCATTTCCATATT[A/G]CTTCTTCATAAAAAG	84708
rs112646544	snp	A/G	0.0142736	0.0832652	intron-variant	LNX1	GRCh38.p7	4:53553416	AGTAGGTTTGATTTA[A/G]AGCCCTCCAAATCTG	84708
rs112675733	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53566215	ATTCACCAAAGTTGA[A/C]ATGAAGGAAAAAATG	84708
rs112679820	snp	C/T	0.0185938	0.0946107	intron-variant	LNX1	GRCh38.p7	4:53651223	TTGTGTATCTGAATG[C/T]TCTCCCTCAATCCAA	84708
rs112689467	snp	A/T	0.0252325	0.109451	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508438	AATTTGAGATTTTTT[A/T]AAGACGCCCACTGCA	84708
rs112746971	snp	A/G	0.5	0	intron-variant	LNX1	GRCh38.p7	4:53626215	ATAGAAAATATGTTC[A/G]TTTTCAAGGACTGAG	84708
rs112758350	in-del	-/T	0	0	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53598235	TTTTACTGACTGTGA[-/T]TTTTTTTTTTTTTTT	84708
rs112778100	snp	C/T	0.0166325	0.0896639	intron-variant, utr-variant-3-prime, downstream-variant-500B	LNX1, FIP1L1	GRCh38.p7	4:53459921	ATATTAAGAGACTCA[C/T]ACATTTTTGATATCA	84708
rs112787861	snp	C/T	0.0138799	0.0821421	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53523431	AGTTGGGACTACAGG[C/T]GTGCACCACCACGCC	84708
rs112807083	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53480487	AAAAACTTCAATTAA[G/T]TAATTAAGCTAATAA	84708
rs112810733	snp	A/T	0.5	0	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53521978	CTAACTTTTTCATTA[A/T]TTTTTTTGTAGAGAC	84708
rs112834129	snp	A/C	0.0123036	0.0774623	intron-variant	LNX1	GRCh38.p7	4:53534133	TCTCAGGAGAAGCCT[A/C]GGGCCCAGTTACCCC	84708
rs112838327	in-del	-/A/AGG	0.345704	0.230956	intron-variant	LNX1	GRCh38.p7	4:53539388	TTTAATTTTTGAGAC[-/A/AGG]CTGTCTCACTCTGTC	84708
rs112839755	snp	A/G	0.0146672	0.084371	intron-variant	LNX1	GRCh38.p7	4:53645213	AAGAATCCAGAGGAA[A/G]GGCTCCTTTGGCAAG	84708
rs112887245	snp	A/G	0	0	intron-variant	LNX1	GRCh38.p7	4:53526956	AATCATTATGCTAAA[A/G]CAATAGAAATGAAAC	84708
rs112891399	snp	C/G	0.5	0	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519668	GGTATCTGACACACA[C/G]ACACATGCGCGCACA	84708
rs112903126	snp	A/G	0.040671	0.13668	intron-variant	LNX1	GRCh38.p7	4:53525292	TTTGAGACCAGCCTG[A/G]CCAACAAGGTGAAAC	84708
rs113020466	in-del	-/C	0	0	intron-variant	LNX1	GRCh38.p7	4:53549460	GAGAAGAGGAGGAGG[-/C]AGGTTGAAAGAAACT	84708
rs113035999	snp	A/C	0.0876345	0.190099	intron-variant	LNX1	GRCh38.p7	4:53493266	GCCACCACACCCAGC[A/C]AGAAAATGCCTCTTC	84708
rs113053793	snp	A/G	0.5	0	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53520494	ATCTTTGGGGTCACC[A/G]AGTTCATTTCCTCCA	84708
rs113107410	snp	A/G	0.5	0	intron-variant	LNX1	GRCh38.p7	4:53651659	TGCTGGTCACCCACA[A/G]CCCTACACACCCGTG	84708
rs113116041	snp	A/G	0.0166325	0.0896639	intron-variant	LNX1	GRCh38.p7	4:53481048	GCATCCAAATGAAGA[A/G]GTTAAGGCATTGCCT	84708
rs113189215	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53495795	GTGATACACCTGCCT[C/T]GGCCTCCCAAAGTGC	84708
rs113193199	snp	C/G	0.191461	0.24305	intron-variant	LNX1	GRCh38.p7	4:53561475	TCATGATCCGCCCAC[C/G]TCATCCTCCCAAAGT	84708
rs113223124	snp	C/T	0	0	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519218	GTCTAAGTGTGCGGG[C/T]ACCTCCAGGTGATTT	84708
rs113226138	snp	A/C	0	0	intron-variant	LNX1	GRCh38.p7	4:53528278	TCCGCAGTTTCAGTT[A/C]CCTGTGGTCAACTGC	84708
rs113242141	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53479645	ATGACTTTTCTATCT[A/T]TCTTTTTTCGCCATT	84708
rs113250218	in-del	-/CTAA	0.47709	0.104548	intron-variant	LNX1	GRCh38.p7	4:53616005	TCTTACTAATTCTTT[-/CTAA]CTATTTTTTGTATTC	84708
rs113264363	snp	A/G	0.0166325	0.0896639	intron-variant	LNX1	GRCh38.p7	4:53473738	ACTGAACTCATCTGT[A/G]CAACAAACCCCTGTG	84708
rs113289808	snp	A/G	0	0	intron-variant	LNX1	GRCh38.p7	4:53483568	CAGCTGACCTCATTT[A/G]TCACTTTAGTAAAAG	84708
rs113332758	snp	A/G	0.0174175	0.0916809	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53595661	CCTAGTTAACCAGCC[A/G]GCTCACTTGGGCTTT	84708
rs113334420	snp	C/G	0.00795532	0.062565	intron-variant	LNX1	GRCh38.p7	4:53578244	GCTCTATTGCAAGTA[C/G]AATCATGTGTTGCTT	84708
rs113361137	snp	C/T	0.0146672	0.084371	intron-variant	LNX1	GRCh38.p7	4:53486821	TTATATGATGGAACT[C/T]AGCATTTTGCAGAGC	84708
rs113361839	snp	A/G	0.0103295	0.0711199	intron-variant	LNX1	GRCh38.p7	4:53571316	GAGCCTCCATGCCCC[A/G]CGTAAATTAAGAATC	84708
rs113393997	snp	C/T	0.00716266	0.059414	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53598195	TGCCTGTTCTGCACT[C/T]GTGACATACTCTACT	84708
rs113421075	snp	A/T	0.5	0	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53597445	GTGTTAGAGGGGTGC[A/T]CTCCCCTCACCCCCA	84708
rs113424704	snp	A/C	0.0193772	0.0965046	intron-variant	LNX1	GRCh38.p7	4:53580155	TGGATAGCTTTGATT[A/C]ATAGAGGAAAAAGTC	84708
rs113442164	snp	A/G	0.5	0	intron-variant	LNX1	GRCh38.p7	4:53472214	AAGCTGGAAACCATC[A/G]TTCTCAGCAAACTAT	84708
rs113449560	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53554061	GGGCTGTATAGGAGA[C/T]GGATGACGTCCTTTC	84708
rs113495911	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53588862	AGAGAAGTGACCAGG[G/T]CCCTGGGCACACAAC	84708
rs113551436	snp	A/G	0.00557542	0.0525036	utr-variant-5-prime	LNX1	GRCh38.p7	4:53652218	ACGTCTCAGGAGATA[A/G]TCCGTTTGAGAGCTG	84708
rs113605201	snp	C/T	0.00953873	0.0683987	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53601330	TCCAGTTGTGGCTGT[C/T]CCCCTGAAGTGGCAT	84708
rs113633365	snp	C/T	0.0244538	0.107838	intron-variant, utr-variant-3-prime	LNX1, LOC101928879	GRCh38.p7	4:53576977	TGAAGAGGTTGCTGG[C/T]AAATGCCCTTAATAT	84708
rs113650219	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53472703	AAAAAAAAAAAACAA[A/C]AAACAATGGGGAAGT	84708
rs113675104	snp	C/T	0.00874735	0.0655527	intron-variant	LNX1	GRCh38.p7	4:53479894	TACCTCAAAACCCTA[C/T]ATCAGAAATAAACAT	84708
rs113693300	snp	A/G	0.00755907	0.0610114	intron-variant	LNX1	GRCh38.p7	4:53550383	CCTCCTTCCTTCCAG[A/G]TCCTCGTCCAAATTC	84708
rs113712244	snp	A/T	0.0166325	0.0896639	intron-variant	LNX1	GRCh38.p7	4:53477577	TATAATCCTCTAGCT[A/T]ATGTTCTGTTAACAA	84708
rs113748981	snp	A/G	0	0	intron-variant	LNX1	GRCh38.p7	4:53497278	GAAAACAATTTCGCA[A/G]CAATTGCTGCACTCT	84708
rs113762614	snp	A/G	0	0	intron-variant, downstream-variant-500B	LNX1, FIP1L1	GRCh38.p7	4:53462759	TCATACATACACATC[A/G]TCTATAACAATTTCT	84708
rs113783745	snp	C/G	0.318656	0.240388	intron-variant	LNX1	GRCh38.p7	4:53606643	tcaaaacctggcaga[C/G]atacaataaaaaaag	84708
rs113793240	in-del	-/A	0.5	0	intron-variant	LNX1	GRCh38.p7	4:53532320	ATCTCTACTAAAAAT[-/A]CAAAAATTAGCCGGG	84708
rs113885098	in-del	-/A	0.170408	0.236992	intron-variant	LNX1	GRCh38.p7	4:53612657	AGACCCTGTCTCTAC[-/A]AAAAAATACAAAAAT	84708
rs113885431	snp	A/C	0.5	0	intron-variant	LNX1	GRCh38.p7	4:53584569	CACGAATGATAAATG[A/C]GATCTGGACAAGTGG	84708
rs113915420	snp	C/T	0.00438332	0.0466095	intron-variant	LNX1	GRCh38.p7	4:53640242	CGACTGTCAGGAAGG[C/T]GAGGAAGCACTGCCT	84708
rs113915759	in-del	-/AC	0.0460142	0.144533	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53514661	AAGATTTGGGTGAGG[-/AC]ACAGTCAAACCATAT	84708
rs113935786	snp	A/C	0.00835141	0.0640778	intron-variant	LNX1	GRCh38.p7	4:53579013	TCAGACATATCAGAG[A/C]CTTGCTGCTGAATGG	84708
rs113956699	snp	G/T	0.220544	0.248259	intron-variant	LNX1	GRCh38.p7	4:53474992	AGGCTGGTCTTGAAC[G/T]CCTGGTCTCAAGTGA	84708
rs113963378	snp	A/C/G/T	0.000173465	0.00931152	missense, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573975	CACACAGGGGTTCAG[A/C/G/T]ATCGTTGGCAGACTC	84708
rs114103555	snp	C/T	0.00874735	0.0655527	intron-variant	LNX1	GRCh38.p7	4:53585600	ATTCAATGACAGATG[C/T]CCTTAGACACTTATA	84708
rs114110249	snp	A/C/G	0.00557542	0.0525036	intron-variant	LNX1	GRCh38.p7	4:53628252	AACTATGCATCCAAC[A/C/G]AAGTATTAGTATTCA	84708
rs114141429	snp	A/G	0.00914312	0.0669923	intron-variant	LNX1	GRCh38.p7	4:53480583	CATCACGGAGTCCTT[A/G]TCCATAAAATGTTTT	84708
rs114143863	snp	A/G	0.0103295	0.0711199	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507907	AAAAACATTTACAGA[A/G]CTTTCCACAGTAAGT	84708
rs114149929	snp	C/T	0.0271762	0.113356	intron-variant	LNX1	GRCh38.p7	4:53550461	AACACTTTTTTTTCC[C/T]CTTTTCAATTTTGAT	84708
rs114154411	snp	A/T	0.0107246	0.0724382	intron-variant	LNX1	GRCh38.p7	4:53526384	TGAATTACCAACTGA[A/T]CAAACCACCAAACCC	84708
rs114157402	snp	C/T	0.00993419	0.0697739	intron-variant	LNX1	GRCh38.p7	4:53540117	GACAACATGGTGGCT[C/T]ACATCTGTAATCCCA	84708
rs114174923	snp	C/T	0.0197687	0.0974348	intron-variant	LNX1	GRCh38.p7	4:53616252	TTTTTTCTTAGAAAC[C/T]TAGATAGACACCTTC	84708
rs114175780	snp	A/T	0.0158469	0.0875917	intron-variant	LNX1	GRCh38.p7	4:53641788	AACATTGTGTATTCT[A/T]TTTGGTGTCTGGCTT	84708
rs114180216	snp	A/G	0.0314385	0.121371	intron-variant	LNX1	GRCh38.p7	4:53582120	AAAACTGTGGTTTGG[A/G]TGCAGCTCTGCTACC	84708
rs114187185	snp	C/T	0.0197687	0.0974348	intron-variant	LNX1	GRCh38.p7	4:53639026	TCTACCAAAAAGACA[C/T]ATACTTGCATGTTCA	84708
rs114222480	snp	A/T	0.02016	0.0983543	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507262	TTGCGTCATCCCTGA[A/T]GTCCCCCTGGAAGCC	84708
rs114241705	snp	C/T	0.00676609	0.0577691	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508306	CCTCTTCAAATACAA[C/T]TGAAGAATGTATAAT	84708
rs114241867	snp	A/T	0.00318978	0.0398085	intron-variant	LNX1	GRCh38.p7	4:53544750	GACACTGATCAATAA[A/T]GCCCATGCGCCAGGC	84708
rs114260591	snp	A/G	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53630992	CAACCTGGGCAAGCC[A/G]GTCAGGTAAACCAAC	84708
rs114266556	snp	C/T	0.0228947	0.104514	intron-variant	LNX1	GRCh38.p7	4:53537206	GGCAGCTAACTTGCA[C/T]GAACATCTGACGCTT	84708
rs114290771	snp	C/G	0.021333	0.101051	intron-variant	LNX1	GRCh38.p7	4:53631478	CTATTATCCATAGAG[C/G]CCTCTTTTCCTCTTC	84708
rs114294397	snp	A/T	0.00438332	0.0466095	intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53574927	AAGCTAGAGCTCCTA[A/T]AAGGGGCCTTTAAGC	84708
rs114337634	snp	A/G	0.0197687	0.0974348	intron-variant	LNX1	GRCh38.p7	4:53583860	GGGTTTGTTTGTAAA[A/G]ACTCTGTAACAGAAA	84708
rs114356062	snp	C/T	0.0352966	0.128072	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498531	GAAAGTCACTATCCA[C/T]ATTTATTTTACCATT	84708
rs114373398	snp	G/T	0.0193772	0.0965046	intron-variant	LNX1	GRCh38.p7	4:53628540	TGGCTGGAATGTAAA[G/T]CACAACCTCTATAGA	84708
rs114391945	snp	A/G	0.00914312	0.0669923	intron-variant	LNX1	GRCh38.p7	4:53551369	GTTGAAGCCAGGGCC[A/G]GGCAGTTTCCCAATA	84708
rs114395204	snp	A/G	0.0383715	0.133092	intron-variant	LNX1	GRCh38.p7	4:53645010	TCTTGCCAACAGCAG[A/G]AGAGTGAGCCCAGGA	84708
rs114399834	snp	C/T	0.0185938	0.0946107	intron-variant	LNX1	GRCh38.p7	4:53538072	ACATAGCAATTGGTT[C/T]CAACCAACCATTGGC	84708
rs114454567	snp	C/T	0.00795532	0.062565	intron-variant	LNX1	GRCh38.p7	4:53486249	GCTCCTGGCAGAGCA[C/T]CATATTGATGCCAAA	84708
rs114455329	snp	C/T	0.00461137	0.0477956	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461066	AAAAACAAAACAAGA[C/T]ATGATTAGTATTTTA	84708
rs114476699	snp	C/T	0.00795532	0.062565	intron-variant	LNX1	GRCh38.p7	4:53614908	GAATCTGGCTCCCTT[C/T]TATTTTACTAAAACA	84708
rs114483620	snp	C/T	0.0205511	0.0992634	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53517907	AGTATGAACTTGAGG[C/T]TGAATGGCCCTCGCC	84708
rs114497566	snp	C/T	0.0205511	0.0992634	utr-variant-5-prime	LNX1	GRCh38.p7	4:53652366	CCCCTGCCCCTTCTG[C/T]AAGGCTTTGAGTAGA	84708
rs114508237	snp	A/G	0.00557542	0.0525036	intron-variant	LNX1	GRCh38.p7	4:53586192	TATGTTGTGGAAGAT[A/G]TAATATAAGTCAGAC	84708
rs114593513	snp	C/T	0.0352966	0.128072	intron-variant	LNX1	GRCh38.p7	4:53497497	CTCACCACCTTTGTC[C/T]AAGCACAGGTGAGGA	84708
rs114623553	snp	C/T	0.0166325	0.0896639	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53521501	GTGTTCTTCCTTGCT[C/T]GGGGTTTGGAAACGT	84708
rs114630067	snp	G/T	0.0115144	0.0749975	intron-variant	LNX1	GRCh38.p7	4:53641209	GGGGAAGGGCGGGGT[G/T]GGGGGGCACCTCCTT	84708
rs114656663	snp	C/T	0.0023933	0.0345097	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53520458	CGCCAGAATCGTTTG[C/T]TCATTCTGTGAGTCT	84708
rs114683329	snp	C/G	0.0372196	0.131242	intron-variant	LNX1	GRCh38.p7	4:53497962	GGGAGGGGTTTCTTG[C/G]CACTTTTGGCAAACA	84708
rs114687347	snp	A/G	0.0197687	0.0974348	intron-variant	LNX1	GRCh38.p7	4:53493807	TGGATAATTGAGAAT[A/G]CTTCTTAAGGCCGCT	84708
rs114688619	snp	C/T	0.0126979	0.078662	intron-variant	LNX1	GRCh38.p7	4:53572025	AAGAAATGAACACAG[C/T]TCCCCAGCACAAATG	84708
rs114707189	snp	A/G	0.0150606	0.0854603	intron-variant	LNX1	GRCh38.p7	4:53528491	TTTGAGATAGACCAC[A/G]TATGCACAATTATTA	84708
rs114713006	snp	C/T	0.0189856	0.0955633	intron-variant	LNX1	GRCh38.p7	4:53480585	TCACGGAGTCCTTAT[C/T]CATAAAATGTTTTAG	84708
rs114817610	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53601569	CAGCTGTGACAACTG[C/G]GTGAGCCTGGTAGCA	84708
rs114820452	snp	A/G	0.0197687	0.0974348	intron-variant	LNX1	GRCh38.p7	4:53583761	AGTTTTAGAAGTCAG[A/G]GAATGCCTTTCATAA	84708
rs114894604	snp	A/G	0.0134861	0.0810011	intron-variant	LNX1	GRCh38.p7	4:53611834	TGTTATATAATGGGG[A/G]TAGGACAAACCCTCC	84708
rs114898573	snp	A/G	0.00557542	0.0525036	intron-variant	LNX1	GRCh38.p7	4:53495844	CCACCACGCCCAGCC[A/G]AGTAATGTTCTTACC	84708
rs114902663	snp	C/T	0.0130921	0.0798413	upstream-variant-2KB	LNX1	GRCh38.p7	4:53653458	CTGGATGTTATCTTA[C/T]GTATATGCAACATGC	84708
rs114905343	snp	A/G	0.0209421	0.100162	intron-variant	LNX1	GRCh38.p7	4:53615088	TTGCTGAAAGAAACA[A/G]TAGAGATAATTACAC	84708
rs114905757	snp	G/T	0.00755907	0.0610114	intron-variant	LNX1	GRCh38.p7	4:53581465	CCATTTTCATACTGC[G/T]ATGAAGAAATTACCC	84708
rs114907164	snp	G/T	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53640557	AATAAAGAATCAAAA[G/T]TGCTTTTGTTTAAGC	84708
rs114919445	snp	A/T	0.00993419	0.0697739	intron-variant	LNX1	GRCh38.p7	4:53525715	ACAGGCAGCCTCAGT[A/T]AGGGGAGGTTCTTCT	84708
rs114923484	snp	C/T	0.00755907	0.0610114	intron-variant	LNX1	GRCh38.p7	4:53493330	GGCATGAGCTCGGGC[C/T]CTCTAGGGCAGATGA	84708
rs114941612	snp	C/T	0.00358779	0.0422022	intron-variant	LNX1	GRCh38.p7	4:53581983	TTTTTTTAAATATTG[C/T]ATTCACATTAGGATT	84708
rs114988530	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53551314	CAACCATCAGGTGAT[A/G]GTCAGGCAGTTGTTA	84708
rs115028904	snp	C/T	0.114036	0.209795	intron-variant	LNX1	GRCh38.p7	4:53548151	TCGGGGGAAATATGA[C/T]TATGAGAAAAGGATG	84708
rs115031027	snp	A/C/T	0.00398564	0.0444627	intron-variant	LNX1	GRCh38.p7	4:53554357	TTTGGCCCAACATTA[A/C/T]GAATTGGTTTGGCCA	84708
rs115039213	snp	C/T	0.0614824	0.164198	intron-variant	LNX1	GRCh38.p7	4:53556464	AAACCAACATAGCAA[C/T]GAAGAAGGATAGCGC	84708
rs115043341	snp	C/T	0.00914312	0.0669923	intron-variant	LNX1	GRCh38.p7	4:53629844	AAAATATTGCAGGTA[C/T]GCCTTGGTTTGATTT	84708
rs115045950	snp	C/T	0.00358779	0.0422022	intron-variant	LNX1	GRCh38.p7	4:53650078	TATAGATGAGCAGAC[C/T]GAGTGGAATAGAATG	84708
rs115072812	snp	C/T	0.0178098	0.0926698	intron-variant	LNX1	GRCh38.p7	4:53464672	ACTACAATAAGTTGA[C/T]ACTGCTACTTGCAGA	84708
rs115095304	snp	A/G	0.0197687	0.0974348	intron-variant	LNX1	GRCh38.p7	4:53489417	TGGGGTCATACAGAT[A/G]TCAGTGACAAGGGCA	84708
rs115101712	snp	C/T	0.084364	0.187256	intron-variant	LNX1	GRCh38.p7	4:53583793	CAGGTTAGAGAAGAG[C/T]GTTCCTTCTCTTGAC	84708
rs115122786	snp	A/G	0.00358779	0.0422022	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507800	GTCAGATTACACACA[A/G]TTTTAATGATTGGAG	84708
rs115123099	snp	C/T	0.00318978	0.0398085	intron-variant	LNX1	GRCh38.p7	4:53551459	GTGGACTCAAGCATG[C/T]GCACTAAGAGGCAAA	84708
rs115138603	snp	A/T	0.00478085	0.0486577	intron-variant	LNX1	GRCh38.p7	4:53537249	AACACCAAACAAATT[A/T]TAAAGGAAGTAAAAG	84708
rs115161882	snp	A/G	0.0134861	0.0810011	upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53592163	ATCTCGGCTGGCTTG[A/G]CAGTTAGAGTCATAC	84708
rs115173903	snp	A/G	0.00795532	0.062565	intron-variant	LNX1	GRCh38.p7	4:53651261	CTTTATGTTGAGCTC[A/G]TTTGAAGCTCACCTC	84708
rs115185527	snp	A/G	0.00636936	0.0560724	intron-variant	LNX1	GRCh38.p7	4:53553865	TTTAAAGAAGGAAAG[A/G]CCCTGGTATAAACAC	84708
rs115223877	snp	C/T	0.0209421	0.100162	intron-variant	LNX1	GRCh38.p7	4:53485233	GGTCAAAACCCCAAT[C/T]ACTGAGCTCGAATTT	84708
rs115228983	snp	A/G	0.0209421	0.100162	intron-variant	LNX1	GRCh38.p7	4:53613478	AAGCCTAGTATCCAT[A/G]TTTGTTATTTTTCCT	84708
rs115243128	snp	C/T	0.0197687	0.0974348	intron-variant	LNX1	GRCh38.p7	4:53579018	CATATCAGAGCCTTG[C/T]TGCTGAATGGAGAAG	84708
rs115295366	snp	A/T	0.0130921	0.0798413	intron-variant	LNX1	GRCh38.p7	4:53636559	AAAATGGAGATGATA[A/T]TGCCCATATTGTGGT	84708
rs115313586	snp	A/G	0.00676609	0.0577691	intron-variant	LNX1	GRCh38.p7	4:53533722	ATTTTTGATTGCCAC[A/G]ATTTGGGAGGGTGCT	84708
rs115324897	snp	A/C	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53535877	CTACATTTGATATGA[A/C]CCCTGATAACTGTTG	84708
rs115342620	snp	A/G	0.0103295	0.0711199	intron-variant	LNX1	GRCh38.p7	4:53526544	GCTTTTCACAATAAC[A/G]GTGATGAGAGGCTTT	84708
rs115350887	snp	C/G	0.0368353	0.130617	intron-variant	LNX1	GRCh38.p7	4:53483137	TGGGGGTGGGTCTTT[C/G]CCATGCTGTTCTCGA	84708
rs115370757	snp	C/T	0.107694	0.205546	intron-variant	LNX1	GRCh38.p7	4:53530201	ACTTTCCCAAACATT[C/T]GTTAAGATTATTTTT	84708
rs115372520	snp	A/G	0.0111196	0.0737302	intron-variant	LNX1	GRCh38.p7	4:53573212	TGGAGACAAAAAGTG[A/G]AATGGTGGCTGCCAG	84708
rs115417696	snp	C/T	0.0197687	0.0974348	intron-variant	LNX1	GRCh38.p7	4:53495487	TCGAAGTCACCTGGA[C/T]TTAGCCATGGAGACT	84708
rs115431490	snp	C/T	0.0189856	0.0955633	intron-variant	LNX1	GRCh38.p7	4:53473215	AGGAAGATGAGACAA[C/T]AGAAGAAATGAGCCA	84708
rs115451817	snp	A/G	0.0221141	0.102801	intron-variant	LNX1	GRCh38.p7	4:53552998	TCAATATTCCCTTCC[A/G]TAGAAACCAACCAGG	84708
rs115454401	snp	A/G/T	0.0158469	0.0875917	intron-variant	LNX1	GRCh38.p7	4:53633925	GCTACTTCACAAAGG[A/G/T]TCTCCTAGAGTTCCT	84708
rs115462069	snp	C/T	0.0123036	0.0774623	upstream-variant-2KB	LNX1	GRCh38.p7	4:53653527	AATCACAGGTGGTGC[C/T]GCTGGCTGCGGTGCC	84708
rs115506292	snp	A/G	0.0256215	0.110247	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53510157	CAAAAAGGATTGCCT[A/G]TTTCATGCCAAGCAA	84708
rs115507348	snp	G/T	0.00597247	0.0543191	intron-variant	LNX1	GRCh38.p7	4:53524098	CATTGTTCTCTTACT[G/T]TTAATAGTATTAATA	84708
rs115510168	snp	G/T	0.00755907	0.0610114	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53514716	TATCTACACTAATCA[G/T]ATGACTCAGGCCATC	84708
rs115548765	snp	C/T	0.0158469	0.0875917	intron-variant	LNX1	GRCh38.p7	4:53649599	ACCCTGAGGTAGCTC[C/T]TGATATTCTCTATCA	84708
rs115588745	snp	C/T	0.00716266	0.059414	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53505763	ATGAAACATGATCAT[C/T]GCTGATACAGGTGCT	84708
rs115589697	snp	C/T	0.0126979	0.078662	intron-variant	LNX1	GRCh38.p7	4:53528028	TAAGTTTATTTAATA[C/T]TCAGAATTCAGGATT	84708
rs115612878	snp	A/G	0.00438332	0.0466095	intron-variant	LNX1	GRCh38.p7	4:53639669	GCTGTTTCTTCTGTC[A/G]CCCACTTACCAGCTG	84708
rs115613709	snp	C/G/T	0.02016	0.0983543	intron-variant	LNX1	GRCh38.p7	4:53584718	TCATAGGATTTTGAT[C/G/T]GGTTAAGGAACTTAG	84708
rs115637472	snp	A/T	0.0193772	0.0965046	intron-variant	LNX1	GRCh38.p7	4:53538500	AATGCATGAGGGTTC[A/T]TCGTTGAAAAACCAC	84708
rs115639083	snp	A/G	0.029116	0.117091	intron-variant	LNX1	GRCh38.p7	4:53642293	TGAAGTTCTTGGGAT[A/G]TTAAAAATGAAAGAA	84708
rs115667460	snp	C/G	0.0115144	0.0749975	intron-variant	LNX1	GRCh38.p7	4:53634678	TGCAGGAAGGGTGGG[C/G]ACATGACCCAGCCTC	84708
rs115673147	snp	C/G	0.0185938	0.0946107	intron-variant	LNX1	GRCh38.p7	4:53531920	AATGTTTAGGGAACA[C/G]ACACAGTGAGTCCTC	84708
rs115685301	snp	C/T	0.0134861	0.0810011	intron-variant	LNX1	GRCh38.p7	4:53525224	GAGCAGTGGCTCACA[C/T]ACATCCCAGCACCTT	84708
rs115692427	snp	C/T	0.0193772	0.0965046	intron-variant	LNX1	GRCh38.p7	4:53630243	AGAATTGGGTATTTA[C/T]ACAGTCGAGCCTATT	84708
rs115699873	snp	C/T	0.0146672	0.084371	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53597619	GTGAGCCAGAGCTTT[C/T]GTCTGTGGCTCCACA	84708
rs115734833	snp	C/T	0.00953873	0.0683987	intron-variant	LNX1	GRCh38.p7	4:53480433	TGACTTAGAATATGA[C/T]GTATTCTAGTTAATT	84708
rs115740006	snp	A/G	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53633408	TTATTGCTTCTTCCC[A/G]GGATTTCTTCATCTC	84708
rs115741120	snp	A/T	0.0158469	0.0875917	intron-variant	LNX1	GRCh38.p7	4:53641565	AGGGGTTCAACCTAA[A/T]GCACATATTTAATTT	84708
rs115742775	snp	C/T	0.00953873	0.0683987	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53595348	GACTGTAAAGAGCCT[C/T]GGGAACCTCAAGGGC	84708
rs115752654	snp	A/G	0.00636936	0.0560724	intron-variant	LNX1	GRCh38.p7	4:53640211	TCTTTGTAGATTTAC[A/G]TATTAAAAACAAGAA	84708
rs115798100	snp	C/T	0.0123036	0.0774623	intron-variant	LNX1	GRCh38.p7	4:53530487	CATGTATCAAATCAG[C/T]GATGATAACATCCAT	84708
rs115799265	snp	A/T	0.0178098	0.0926698	intron-variant	LNX1	GRCh38.p7	4:53483159	TGTTCTCGAGATAGT[A/T]AGTCTCACGAGATCT	84708
rs115803821	snp	A/G	0.0166325	0.0896639	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507856	GCGAATTGGACATTG[A/G]GTTCCTGCCAAAACT	84708
rs115872114	snp	A/T	0.0352966	0.128072	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508963	AATCCAGAAAACTCC[A/T]CAAAAACCAAACTTT	84708
rs115885793	snp	A/T	0.0197687	0.0974348	intron-variant	LNX1	GRCh38.p7	4:53631929	TTAGATGTTTGAAAA[A/T]TTTAAGTAAAATCTG	84708
rs115906984	snp	A/C	0.0197687	0.0974348	intron-variant	LNX1	GRCh38.p7	4:53493396	GACACCACCAAGTGG[A/C]ACAGCTCAAAAGCTA	84708
rs115919672	snp	C/T	0.0111196	0.0737302	intron-variant	LNX1	GRCh38.p7	4:53549208	CTTAAAGCTTCTGGG[C/T]AACAAGGTCATAAAA	84708
rs115921949	snp	C/T	0.0197687	0.0974348	intron-variant	LNX1	GRCh38.p7	4:53490547	GGTTAGAGCTCAACA[C/T]ATGTAAAGCTGGTCA	84708
rs115931379	snp	C/G	0.02016	0.0983543	utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460757	CATATTTTCTGAGGT[C/G]TAACTGGCTTTCATT	84708
rs115938011	snp	A/G	0.00755907	0.0610114	intron-variant	LNX1	GRCh38.p7	4:53619689	CATGTGAAAGTTTTC[A/G]CAAGAACCAATGTTT	84708
rs115948594	snp	A/C	0.00358779	0.0422022	intron-variant	LNX1	GRCh38.p7	4:53648953	AGATCATGGTGAATG[A/C]AAAACCAATAGAAGA	84708
rs115978786	snp	C/T	0.0126979	0.078662	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53503494	AGGATGCATTATCAA[C/T]GAGTAGCAATATTTT	84708
rs115982320	snp	C/T	0.0221141	0.102801	intron-variant	LNX1	GRCh38.p7	4:53537928	GAGTTGCATCTGTAC[C/T]TCTCTGAGGACAGAA	84708
rs115993470	snp	A/G	0.0193772	0.0965046	intron-variant	LNX1	GRCh38.p7	4:53483963	GTAGGGCCTTTGGGA[A/G]GTGATTAGGTCATGA	84708
rs116007637	snp	C/T	0.00438332	0.0466095	intron-variant	LNX1	GRCh38.p7	4:53571626	GTCCACCGAGATGTA[C/T]GTTAGACCTCTGACC	84708
rs116044609	snp	A/C	0.00438332	0.0466095	intron-variant	LNX1	GRCh38.p7	4:53530867	GGGGTACAGGGAATT[A/C]AAATTGTAAAATGAG	84708
rs116045380	snp	C/T	0.00318978	0.0398085	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53506538	AACCTCTCTGTGCCA[C/T]AGTTTCCTCATCTGT	84708
rs116046382	snp	A/G	0.0448719	0.142907	intron-variant	LNX1	GRCh38.p7	4:53473386	ATTTACAATAGCAAA[A/G]ATACAGAATCAACCT	84708
rs116058945	snp	A/C/T	0.0213452	0.101169	intron-variant	LNX1	GRCh38.p7	4:53564051	GAGAGCTGCTGTGGG[A/C/T]GCCTGTGAAGGACTC	84708
rs116065787	snp	A/T	0.00597247	0.0543191	intron-variant	LNX1	GRCh38.p7	4:53529169	AAACAACACGAGAAA[A/T]CTTAGAAAACCAAAA	84708
rs116068599	snp	C/T	0.0154538	0.0865337	intron-variant	LNX1	GRCh38.p7	4:53634950	CCTGCCTCAGCTTCC[C/T]ATGTTGCTGGGACTA	84708
rs116095427	snp	A/G	0.00953873	0.0683987	intron-variant	LNX1	GRCh38.p7	4:53495311	AGTGACCCTGACGAA[A/G]TCAACAAAATACATA	84708
rs116100576	snp	C/T	0.0178098	0.0926698	intron-variant	LNX1	GRCh38.p7	4:53483835	CCATGCTCTTTTGCA[C/T]TGACTCAGACAATGG	84708
rs116109212	snp	C/T	0.0115144	0.0749975	intron-variant	LNX1	GRCh38.p7	4:53550251	TAAACATGTGCTGAA[C/T]TGAAATGCTTCGAGA	84708
rs116118081	snp	C/G	0.00636936	0.0560724	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53515200	AGAGAAGTGTTGGCT[C/G]ATGGAGTCCCACATC	84708
rs116132390	snp	C/T	0.0107246	0.0724382	intron-variant	LNX1	GRCh38.p7	4:53613283	GTGTGTTTCCATACA[C/T]GAAGAAATCACCTTG	84708
rs116140925	snp	C/G	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53473023	TTTTTGTGACTCTCA[C/G]GCCTTGACTATGAAA	84708
rs116152434	snp	A/C	0.00597247	0.0543191	intron-variant	LNX1	GRCh38.p7	4:53555655	ATGTGTCACTAATTC[A/C]CTGATTAATTATCCC	84708
rs116153369	snp	A/G	0.00557542	0.0525036	intron-variant	LNX1	GRCh38.p7	4:53534111	GGACCTATCAGAAAG[A/G]GATGGTTCTCAGGAG	84708
rs116172001	snp	A/C/G	0.00975461	0.069154	missense	LNX1	GRCh38.p7	4:53481842	CGACGAGGTGAACAC[A/C/G]TCTTTCACTGGCCTG	84708
rs116179143	snp	A/T	0.00835141	0.0640778	intron-variant	LNX1	GRCh38.p7	4:53551422	TGATCAGCTTCCTAG[A/T]AAGATCTCAGGAGTT	84708
rs116185707	snp	A/G	0.021333	0.101051	intron-variant	LNX1	GRCh38.p7	4:53619708	GAACCAATGTTTTCA[A/G]TTCTACTGGACATAA	84708
rs116199088	snp	A/G	0.00953873	0.0683987	intron-variant	LNX1	GRCh38.p7	4:53541233	TCTAGTGAGTGGGTG[A/G]AGGTAACAACCAAGT	84708
rs116211287	snp	C/T	0.0352966	0.128072	intron-variant	LNX1	GRCh38.p7	4:53473817	ATTTTGCTTTCTTGG[C/T]TTTTAACTTTTATTT	84708
rs116218900	snp	A/G	0.0126979	0.078662	intron-variant	LNX1	GRCh38.p7	4:53644766	GAGGTTCCTGCTGGA[A/G]GGAGCTCAGAGTATA	84708
rs116244605	snp	A/G	0.021333	0.101051	intron-variant	LNX1	GRCh38.p7	4:53466494	TGCCAGACGGTGCAG[A/G]ACAGTGGGTGCAGCA	84708
rs116274861	snp	C/T	0.00795532	0.062565	intron-variant	LNX1	GRCh38.p7	4:53630122	GGGTGGGAATAACAA[C/T]CATGTAAGTTTTCCC	84708
rs116275534	snp	G/T	0.0829062	0.185956	intron-variant	LNX1	GRCh38.p7	4:53552857	AAAAGACTTAAATAT[G/T]TAAAGGAATGTTACA	84708
rs116310072	snp	A/T	0.00597247	0.0543191	intron-variant	LNX1	GRCh38.p7	4:53544193	AGGTGCTGATTTCTC[A/T]CTCTCTCTCTCTTTT	84708
rs116329440	snp	G/T	0.0209421	0.100162	intron-variant	LNX1	GRCh38.p7	4:53473462	TACATCATGGAATAC[G/T]ATGCAGTCATAAAGA	84708
rs116337493	snp	A/G	0.0170251	0.090679	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53510296	ATTATTTAACTGATG[A/G]CACATTTTAAAATGT	84708
rs116339968	snp	C/T	0.0372196	0.131242	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53504609	CTTGGCTGTTTGGCA[C/T]GAGAGGCCTAGCTTT	84708
rs116365567	snp	C/T	0.0178098	0.0926698	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53600155	GCAAATTACTATTTT[C/T]CTCACATCAATCCTC	84708
rs116401356	snp	A/T	0.00358779	0.0422022	intron-variant	LNX1	GRCh38.p7	4:53590016	TTAGATGCACTTTTA[A/T]CAGAAGATCCAAGCT	84708
rs116435486	snp	A/C	0.0197687	0.0974348	intron-variant	LNX1	GRCh38.p7	4:53638499	GGGATGCACGTGTTC[A/C]CAGCTGAGGTCCAAC	84708
rs116509095	snp	C/T	0.00159617	0.0282053	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53521066	GCTATGGATCAACGG[C/T]GCTTTCTATTTCAGG	84708
rs116520234	snp	C/T	0.0205511	0.0992634	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53509532	GATCTAGGGAAATTT[C/T]ATTTACCTGGCTAAA	84708
rs116520390	snp	A/C/T	0.00628829	0.0557197	intron-variant	LNX1	GRCh38.p7	4:53478533	TTGATTCTCTGCCAC[A/C/T]CCAGTGCCTTTAAAA	84708
rs116523473	snp	G/T	0.00835141	0.0640778	intron-variant	LNX1	GRCh38.p7	4:53614633	TAGAATTTTAGACTT[G/T]CCTAAGTTGTGAAAT	84708
rs116556143	snp	C/T	0.0197687	0.0974348	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53504398	CTCTCTCAGCCTTCA[C/T]AGAATCAAAGAAAGT	84708
rs116557129	snp	A/G	0.0115144	0.0749975	intron-variant	LNX1	GRCh38.p7	4:53634749	GCTCCGAGGGGTGGC[A/G]GTTTACTAAGTCAAT	84708
rs116656453	snp	A/G	0.0138799	0.0821421	intron-variant	LNX1	GRCh38.p7	4:53630747	CTTATGTATTGATTG[A/G]CTGATAAAAATGTTG	84708
rs116675773	snp	C/T	0.0178098	0.0926698	intron-variant	LNX1	GRCh38.p7	4:53497822	TGCTTTAGGTTATTT[C/T]TCCTCTTATTCCAAT	84708
rs116704069	snp	A/G	0.0209421	0.100162	intron-variant	LNX1	GRCh38.p7	4:53485299	CCCAGCAGAGTGTCC[A/G]TAGGCTTGCAAATTG	84708
rs116708357	snp	G/T	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53583040	AAATAATTGCCAAAG[G/T]TAGGGCAAAGTCTAT	84708
rs116715607	snp	A/G	0.0115144	0.0749975	intron-variant	LNX1	GRCh38.p7	4:53587290	TCCTGATTTCAGCTC[A/G]GTGTAGTTTTCCACA	84708
rs116735529	snp	C/T	0.00438332	0.0466095	intron-variant	LNX1	GRCh38.p7	4:53537775	ACCCTGTAATACAGT[C/T]AAGGAAGAGAATGTC	84708
rs116740871	snp	C/G/T	0.0197687	0.0974348	intron-variant	LNX1	GRCh38.p7	4:53637952	GAAGCAAGAGAGAAG[C/G/T]CTCCCACTGTGTATT	84708
rs116743508	snp	G/T	0.0142736	0.0832652	intron-variant	LNX1	GRCh38.p7	4:53606060	AAACAAGAGCAAACC[G/T]ACACACAGTTAGCAG	84708
rs116744860	snp	C/T	0.00404952	0.0448147	missense, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573978	ACAGGGGTTCAGGAT[C/T]GTTGGCAGACTCTGG	84708
rs116771817	snp	A/G	0.00279162	0.0372561	intron-variant	LNX1	GRCh38.p7	4:53495519	AGACTTACTCTGTCC[A/G]TAGGATCCCTGGAGA	84708
rs116778496	snp	C/T	0.0260105	0.111035	intron-variant	LNX1	GRCh38.p7	4:53628430	AATGCAAATTAAAAC[C/T]ATGATGAGACACCAT	84708
rs116797242	snp	C/G	0.0126979	0.078662	intron-variant	LNX1	GRCh38.p7	4:53491471	TCCAAGCTCTACCAG[C/G]CCAGGAACTGTACCA	84708
rs116822991	snp	A/T	0.00318978	0.0398085	intron-variant	LNX1	GRCh38.p7	4:53626155	AGGCCACATGTCACA[A/T]GATTCCATTTAAAAG	84708
rs116837952	snp	A/T	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53612452	CTTTACTTTGTTTTG[A/T]TTTTGCAAATTAGAA	84708
rs116839884	snp	C/T	0.0267878	0.112589	intron-variant	LNX1	GRCh38.p7	4:53581385	ATAGTTTTGTTTTCC[C/T]GGCTTTAAAGGAAAC	84708
rs116893512	snp	G/T	0.00914312	0.0669923	intron-variant	LNX1	GRCh38.p7	4:53651328	CGTCAGCATTCCTTG[G/T]GCACCGGACTTGCAC	84708
rs116957885	snp	A/G	0.00636936	0.0560724	intron-variant	LNX1	GRCh38.p7	4:53546768	AAAATAGGAAAGAGG[A/G]GCTGCAGTGTGAGGG	84708
rs116971077	snp	A/G	0.0103295	0.0711199	intron-variant	LNX1	GRCh38.p7	4:53480830	AACATATAGATTGAC[A/G]TAGAAAGAAAAGGGC	84708
rs117135571	snp	A/C	0.00557542	0.0525036	intron-variant	LNX1	GRCh38.p7	4:53532855	CCTTCCCTCAAGGAA[A/C]ACTGCAGGCTGCCCA	84708
rs117278793	snp	C/T	0.00279162	0.0372561	intron-variant	LNX1	GRCh38.p7	4:53561101	CAGGAAAATGTTGGG[C/T]TCAGAGTTAGAAGGT	84708
rs117395833	snp	A/C	0.0327778	0.123752	intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53574378	ATGCCTAAAGTAACT[A/C]TAAAAAATGTAATTT	84708
rs117401196	snp	C/G	0.00383207	0.0436044	intron-variant, missense	LNX1	GRCh38.p7	4:53557888	CAGTTCTGAATACAG[C/G]AAGTGCAGGTTGCCC	84708
rs117447769	snp	G/T	0.00279162	0.0372561	intron-variant	LNX1	GRCh38.p7	4:53539534	CCATGCCCAGCTAAT[G/T]TTTTTAGTTTCTCCT	84708
rs117620663	snp	A/G	0.00716266	0.059414	intron-variant	LNX1	GRCh38.p7	4:53642556	GTCATATGTGGCACG[A/G]TTATTCTTTATATGC	84708
rs117645204	snp	A/G	0.00557542	0.0525036	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53516636	CATGGCAGGTGCCAG[A/G]AATGGTAGATTCTGG	84708
rs117712999	snp	A/T	0.00478085	0.0486577	intron-variant	LNX1	GRCh38.p7	4:53561256	TTTTTTGAGATGGAG[A/T]CTCATTCTGTCACCA	84708
rs117718890	snp	C/G	0.00993419	0.0697739	intron-variant	LNX1	GRCh38.p7	4:53549507	TAATTGCAACGTGTA[C/G]ATTGTATTTAGCTCA	84708
rs117719421	snp	A/G	0.00914312	0.0669923	intron-variant	LNX1	GRCh38.p7	4:53547400	CCCATTTATAGGTGA[A/G]AAAAGCTCAGAGAAG	84708
rs117721596	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53536377	CACACAGTCAAAGTC[A/G]TTCCCTAAGGAACTC	84708
rs117855925	snp	C/T	0.00517822	0.0506191	intron-variant	LNX1	GRCh38.p7	4:53542270	CAGTTTGCATTTAAA[C/T]GATCACAGACAAATT	84708
rs117907046	snp	C/G	0.0337553	0.125452	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53521594	TTCCAGCCAGTTTCT[C/G]TATTTGCTAAATGAG	84708
rs117908527	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53585664	AGGTGATGTGAGGAG[A/G]GAGGCAGAGATTGGA	84708
rs117964991	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53620529	GGTGTTGGGTGCATT[C/T]GGGTTGAGGATTCAA	84708
rs118020895	snp	G/T	0.00914312	0.0669923	intron-variant	LNX1	GRCh38.p7	4:53651329	GTCAGCATTCCTTGG[G/T]CACCGGACTTGCACC	84708
rs118183423	snp	A/G	0.00755907	0.0610114	intron-variant	LNX1	GRCh38.p7	4:53550421	GATGCTCAAAACACA[A/G]GACAAGACAAATCCA	84708
rs118190461	snp	C/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53560214	AAAGGTTGTGGACTT[C/T]ATATTGGTATTGGAT	84708
rs137883311	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53637568	ATTGCTCAATCCCCA[C/T]GACACTGTAAGGTAG	84708
rs137886645	snp	A/G	0.000380212	0.0137827	missense	LNX1	GRCh38.p7	4:53496058	TTTCTGGGCTGCCAT[A/G]TCGAAGATCATGTCC	84708
rs137896863	snp	C/T	0.0228947	0.104514	intron-variant	LNX1	GRCh38.p7	4:53640531	GAAAACACATACATT[C/T]CATTGCTAAAAATAA	84708
rs137948070	in-del	-/A			intron-variant	LNX1	GRCh38.p7	4:53583552	CACCCAAAAATACAG[-/A]AAAAAAAAAACCCTT	84708
rs137976885	snp	C/T	0.00279162	0.0372561	intron-variant	LNX1	GRCh38.p7	4:53650290	GGTGTGGAGGACATA[C/T]GGTAGCTCCAGAATT	84708
rs137982939	snp	A/T	0.0103295	0.0711199	intron-variant	LNX1	GRCh38.p7	4:53528765	AAACTGGGTAAGTTT[A/T]CCTACCCTGGCACCA	84708
rs138021296	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53533322	CTGGGCCCCATTCTC[C/T]CTTTAGCAATTAGAA	84708
rs138053326	snp	A/G	0.00716266	0.059414	intron-variant	LNX1	GRCh38.p7	4:53636552	GAACCATAAAATGGA[A/G]ATGATAATGCCCATA	84708
rs138069784	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53561715	GCCAGCCTTCAGCCA[C/T]GTATGTCTTGGGCCA	84708
rs138076504	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53522204	AACCCATCTCTACCA[C/T]AGGTCTTTGTCCAAT	84708
rs138092169	snp	A/C/G	3.33565e-05	0.00408379	missense, stop-gained, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461562	CAGCTGTGTTTCTTC[A/C/G]TAATACAATATCTTT	84708
rs138093259	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53596607	TTTTGGTGGTGGCTG[C/T]TGCTATTTCGAAGGT	84708
rs138143322	snp	C/T	0.00318978	0.0398085	intron-variant	LNX1	GRCh38.p7	4:53590218	GGAACGACTGTCTGT[C/T]TAAGGCAAAAATGAT	84708
rs138151311	snp	C/G/T	0.00024953	0.0111672	missense	LNX1	GRCh38.p7	4:53481779	CATTGCTGTTCCAGC[C/G/T]GGCTTCCTGAAAGAT	84708
rs138192103	snp	A/G	0.00597247	0.0543191	intron-variant	LNX1	GRCh38.p7	4:53624096	TCTTGAGCTCTTTCC[A/G]TCTGTCCTCCTTACT	84708
rs138193792	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53488570	GATGAACCAGCTGCA[C/T]TGAGGACCTCATTAA	84708
rs138199518	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53518082	AGACAGGAAAAATTC[A/G]AAACAAGCTGGAAAG	84708
rs138203437	snp	C/G/T	0.000399281	0.0141238	upstream-variant-2KB	LNX1	GRCh38.p7	4:53654358	GCTCCTCATCTGCTT[C/G/T]GTGGCTTTTCACCAA	84708
rs138220871	snp	A/G/T	0.0252325	0.109451	intron-variant	LNX1	GRCh38.p7	4:53581673	GACTTACTCACTATC[A/G/T]CAAGAATAGCATGGG	84708
rs138271957	snp	C/G	0.0310518	0.120672	intron-variant	LNX1	GRCh38.p7	4:53650403	GTGGTCATGATGGCA[C/G]TTGATGACATTTGGG	84708
rs138293080	snp	A/G	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53533750	GCTCCTGGCATGTAG[A/G]GGGTAGAGGACAGGG	84708
rs138328090	snp	C/T			intron-variant, utr-variant-3-prime	LNX1, LOC101928879	GRCh38.p7	4:53576585	ACTTCACAGAGCTGA[C/T]ATTCTAGTGGGGCTA	84708
rs138338265	snp	A/G	0.0023933	0.0345097	utr-variant-3-prime, downstream-variant-500B	LNX1, FIP1L1	GRCh38.p7	4:53460377	AACATGGTATTTGAA[A/G]GAATAAATTACTAGG	84708
rs138364209	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53549366	TTTCAGTTACTAGCC[C/G]AGTATTTGGAATTTG	84708
rs138368297	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53593680	TATGGGCTTTTTTTT[G/T]GGGCCATTAGGGCTG	84708
rs138379885	snp	C/G	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53645853	GTATGAAATACCAGA[C/G]TCCTGGGCATGCATT	84708
rs138403769	snp	A/G	0.00279162	0.0372561	intron-variant	LNX1	GRCh38.p7	4:53554161	TTTGCAAGCATTTGC[A/G]GTTCTGTCCAGCTCT	84708
rs138408090	snp	A/G	0.00478085	0.0486577	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53601813	AAGGAATAAGGAACC[A/G]CATGCCAGGGGTCAC	84708
rs138414756	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53528265	CATAGTTTTGCTTTC[C/T]GCAGTTTCAGTTACC	84708
rs138451862	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53500656	CGAGATGTTGTAAAT[G/T]TGGGTCCTTAATCTC	84708
rs138458211	snp	C/G	4.9489e-05	0.00497414	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508198	CTCTTCCTATCTTTG[C/G]TCAGGCCGTAGTGGG	84708
rs138458284	snp	A/G	0.0111196	0.0737302	intron-variant	LNX1	GRCh38.p7	4:53616482	TTAGTACTTGGATTT[A/G]TCACAGAATGAATGG	84708
rs138467169	snp	A/G	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53544446	GTGATCCACCCCTTC[A/G]GCCTCCCAAAGTGCT	84708
rs138480833	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53622672	TCATGAGATTGAAAA[G/T]GTTTAAAAGTGTAAA	84708
rs138484757	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53547640	GGAAGAAAGTCGGGA[A/G]GGGCTCACAGGTACA	84708
rs138502595	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53606059	TAAACAAGAGCAAAC[C/T]GACACACAGTTAGCA	84708
rs138540976	snp	A/C/T	0.00318978	0.0398085	intron-variant	LNX1	GRCh38.p7	4:53633914	AATGTGTGCCAGCTA[A/C/T]TTCACAAAGGGTCTC	84708
rs138598823	snp	C/T	0.00318978	0.0398085	intron-variant	LNX1	GRCh38.p7	4:53494180	GAGTGGTTTCCCCCA[C/T]ACCATTCTTGTGGTA	84708
rs138607270	in-del	-/GTCA			intron-variant	LNX1	GRCh38.p7	4:53616720	AACCTTATCAATATG[-/GTCA]CCATTCACTTTAATT	84708
rs138613905	snp	A/C	0.00358779	0.0422022	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53596321	AGTTTAGGAGGAAAC[A/C]CTTCTCTGGTTTGTG	84708
rs138635997	snp	A/G	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53478370	TTTACTTGCAGGCAA[A/G]TTGGCCTGCAACTAA	84708
rs138671505	in-del	-/AATG	0.0189856	0.0955633	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53462014	CCTTTGAATAATCTC[-/AATG]AAAGCAGTTTAAGCC	84708
rs138707403	snp	C/T	1.71923e-05	0.00293187	missense	LNX1	GRCh38.p7	4:53481839	ACACGACGAGGTGAA[C/T]ACGTCTTTCACTGGC	84708
rs138708314	snp	A/G	0.00914312	0.0669923	intron-variant	LNX1	GRCh38.p7	4:53610355	TTGACCATCTTAAAA[A/G]CCATGAAAGGTCGAA	84708
rs138717214	snp	A/G	0.00835141	0.0640778	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53522031	AATTTCTAGGCACAA[A/G]CAATCCTTCCATCTC	84708
rs138735021	snp	A/C	0.00597247	0.0543191	intron-variant	LNX1	GRCh38.p7	4:53571312	GTGTGAGCCTCCATG[A/C]CCCGCGTAAATTAAG	84708
rs138737055	snp	A/G	0.00318978	0.0398085	intron-variant	LNX1	GRCh38.p7	4:53490246	AGTCTGGAATTGCCT[A/G]TGGAAAAAAGGCTTA	84708
rs138741019	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53637489	TCCTTAATTCCAAAT[A/G]CTTTGCACTACACCT	84708
rs138742127	snp	C/T	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53561881	CCATCATGACACACA[C/T]ACACCTATGTAACAA	84708
rs138761896	snp	A/G	0.00318978	0.0398085	intron-variant	LNX1	GRCh38.p7	4:53639948	TGAGGCACAAAAATT[A/G]CTTGAACCCAGAGGC	84708
rs138763548	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53518399	CTTAATGTTAATGAC[C/T]CTCCTTTAATGCCGA	84708
rs138782850	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53559234	AAGAGTTTAAATACA[C/G]AAGACTCTTAGAATG	84708
rs138792232	snp	C/T	0.0244538	0.107838	intron-variant	LNX1	GRCh38.p7	4:53472122	ACTGGATTAAGAAAA[C/T]GTGGTACATATACAC	84708
rs138813024	snp	A/G	4.94295e-05	0.00497115	synonymous-codon, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498737	GACCAGTGGGGTTTC[A/G]CTACCTCCCACCAGC	84708
rs138909330	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53571710	CTTTGTCACTTAGGC[G/T]GGAGTGCAGTAGCGC	84708
rs138915510	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53491073	TTCTGTTATTAATCT[A/G]CAAAAGCAAAATGCC	84708
rs138930964	snp	G/T	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53553177	GTAGAAGTTCCTGAT[G/T]CATATAGCACTGAGT	84708
rs138951645	snp	A/C	0.0205511	0.0992634	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507892	AACGATTTCCCCTTA[A/C]AAAACATTTACAGAA	84708
rs138962898	in-del	-/A	0.0872718	0.189788	intron-variant	LNX1	GRCh38.p7	4:53618841	ATTTATGTCCCTTTT[-/A]AAAAAAATTTGGTCT	84708
rs138967279	in-del	-/ACTATAAAAACTACGCATTGTTCATTTAAGA			intron-variant	LNX1	GRCh38.p7	4:53464462	ACCTAACAAATATAA[lengthTooLong]AATGTTTTAATATAA	84708
rs138984699	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461798	TGTTTTCCATAATTT[G/T]GAATATCCTTAAAAA	84708
rs138986336	snp	C/G	0.00557542	0.0525036	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53517463	TAATTGAGTCCTGAT[C/G]ATGCTACTTGGAGGA	84708
rs138997594	in-del	-/G	0.00716266	0.059414	intron-variant	LNX1	GRCh38.p7	4:53631163	TTGGAGACAGTTTTA[-/G]TACCCAGGGGGAGAC	84708
rs139022562	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53538986	TCCAGGAGATCTGAC[A/G]GGTTGAAGGGGATCC	84708
rs139051833	in-del	-/A	0.02016	0.0983543	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53504893	GTGGCACGCTAAAAC[-/A]ATTACAATAGTAACG	84708
rs139073479	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53560227	TTCATATTGGTATTG[G/T]ATTGTATTTCTGACG	84708
rs139078390	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53473736	GTACTGAACTCATCT[G/T]TACAACAAACCCCTG	84708
rs139080150	in-del	-/A	0.0441095	0.141807	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53521701	TGCAAACGAAGGGGG[-/A]AAAGGAGGGGATGCT	84708
rs139090978	snp	C/T	0.00795532	0.062565	utr-variant-5-prime, upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53591390	GGTTTCAACTCACCT[C/T]TTCAAGCGACTGTCT	84708
rs139105889	snp	A/C	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53632016	GTGGAGAAGGAGCGG[A/C]CAAAGCTCCTGGGTC	84708
rs139105982	snp	C/T	0.0142736	0.0832652	intron-variant	LNX1	GRCh38.p7	4:53585317	TAGTGATGATGGCTG[C/T]CAATTCTGACTCTCC	84708
rs139119930	snp	A/G	0.0256215	0.110247	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508844	GATCTGAGAAGTGTC[A/G]TTCATTGCCATGTTG	84708
rs139130829	snp	A/G	0.00517822	0.0506191	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53594353	ACATCTTTTATGGTC[A/G]TTTTTCTCTGTAACT	84708
rs139138814	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53465504	AAGTTACATTCTTCT[C/T]CAGCAGCTGCTTTAA	84708
rs139138914	snp	C/G	0.00318978	0.0398085	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519518	CACTGGTTGTATTAG[C/G]CCCATCTTATAGATG	84708
rs139141754	snp	A/G	0.00795532	0.062565	intron-variant	LNX1	GRCh38.p7	4:53589966	GCACTAATCAACCAT[A/G]GTAAACCAGAGGCAA	84708
rs139158365	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53513645	TTCTTTCTCTGGATA[C/T]CCCAAATACAATCCA	84708
rs139163037	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53573137	TGAGATGAGCTGGTC[A/G]CAAAAGGACAAATAC	84708
rs139163655	in-del	-/A	0.495745	0.0459295	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53515520	GGCCCCCACCCCACC[-/A]AAAAAAAAAATGACA	84708
rs139178248	snp	A/T	0.0119091	0.0762411	intron-variant	LNX1	GRCh38.p7	4:53628904	ACTGCATGTTCTCAC[A/T]TATAAGTTGGAGCTA	84708
rs139185442	snp	A/G	0.0209421	0.100162	intron-variant	LNX1	GRCh38.p7	4:53555218	TCATTCCTGCTCCCA[A/G]GCGTGCTAAACTGGC	84708
rs139199297	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53515284	TGCGGGCAAGTTGTG[A/G]CCACAGAGCTATACA	84708
rs139204809	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53509495	GATCTAAATCCTTGC[C/T]CTGAAATTTACATAG	84708
rs139265415	snp	C/G	0.00716266	0.059414	intron-variant	LNX1	GRCh38.p7	4:53643743	GGGCAGCTTGCTAAA[C/G]CTCTTTGAACCTCAG	84708
rs139266392	snp	A/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53600610	ACTAACAGGGTCTCA[A/G]TATAATAATAGGGGA	84708
rs139274061	snp	A/G	0.00755907	0.0610114	intron-variant	LNX1	GRCh38.p7	4:53646821	AGACATCTGTTTCAC[A/G]TTTTACAAAGCATTG	84708
rs139303198	in-del	-/TGTG			intron-variant	LNX1	GRCh38.p7	4:53652010	CTCTCCTCAATTTGA[-/TGTG]TGTGTGTGAGAGAGA	84708
rs139317729	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53648866	TCCCTCCAGCTTTGG[A/G]GTTGTCAGGACAATC	84708
rs139339008	snp	A/G	0.0209421	0.100162	intron-variant	LNX1	GRCh38.p7	4:53466916	GGCTCCATCTCTGGG[A/G]GCAGGGCACAGACAA	84708
rs139368753	snp	A/C	0.00755907	0.0610114	intron-variant	LNX1	GRCh38.p7	4:53637732	AAACCAAAACACAGC[A/C]AGTTTCTGAGATATT	84708
rs139490422	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53625628	ATAGTGACACCCTGT[C/G]TCTACAAAATAAAAA	84708
rs139493245	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53595076	GAAGCAAAAATATTG[A/G]TGTTGGCTGGTGCCA	84708
rs139501766	snp	A/C	0.0322114	0.122752	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519731	GCTATTCTGAGCACT[A/C]TACCCTTTATTCATT	84708
rs139503920	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53608211	GAAAATATTTGTAAA[C/T]TGTGCATCCTACAAA	84708
rs139544141	snp	C/T	0.0134861	0.0810011	intron-variant	LNX1	GRCh38.p7	4:53612574	CTTGTAATCCCAGCA[C/T]TTTGGGAGGCTGAGG	84708
rs139556428	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53486184	AGACTCCCTCTCTCT[C/T]TTCCGCCCTGCGCCA	84708
rs139558462	snp	C/T	0.00676609	0.0577691	intron-variant	LNX1	GRCh38.p7	4:53540339	AGTAAGTCATGACTC[C/T]GCCACTGCACTCCAG	84708
rs139568259	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53578557	CATTGACCAACATGT[C/T]GTTATGGGGTCCATG	84708
rs139570472	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53651001	AACGCTATGAGGGAT[G/T]TATTACCATCATTCT	84708
rs139606192	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53590900	CAGAATTTGCCCTGA[C/G]GAACAGGTTTTCAGG	84708
rs139624578	snp	C/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53549895	TATCCGCCTGACATA[C/G]TCATGGAACTAGAAA	84708
rs139625293	snp	A/C	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53535995	TATTCAGGGACCACA[A/C]TGATAGAAGCCTTGT	84708
rs139628331	snp	A/G	0.00636936	0.0560724	intron-variant	LNX1	GRCh38.p7	4:53464237	ATATGAACTATGACC[A/G]TTAACTTAATAGATT	84708
rs139657717	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53586342	ATAAGCAAGTTATGC[A/C]AATCATCTCAGCAGA	84708
rs139659308	snp	A/G	0.00517822	0.0506191	intron-variant	LNX1	GRCh38.p7	4:53541928	AAAAAATAGGTGAAG[A/G]AATATTTGGCAAACA	84708
rs139688826	snp	A/C	0.0158469	0.0875917	intron-variant	LNX1	GRCh38.p7	4:53648293	TTTTTTTAACTTGAT[A/C]GTAGCCATGCTAATG	84708
rs139696053	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53528681	ATTCCCTGTGGATAA[A/G]GGGGGGACTACTGTA	84708
rs139696663	snp	C/T	0.000461133	0.0151774	missense	LNX1	GRCh38.p7	4:53496130	GTCGATATGCCACAC[C/T]GCCATCCAGCACATT	84708
rs139697976	snp	A/G	0.10237	0.201756	intron-variant	LNX1	GRCh38.p7	4:53545847	GGGTCTTACTCTGTC[A/G]CCCAGGCTGGAGTAC	84708
rs139704869	in-del	-/G	0.00597247	0.0543191	intron-variant	LNX1	GRCh38.p7	4:53583062	AAAGTCTATCTTTCT[-/G]TATTAAACAAAGTAA	84708
rs139716533	snp	A/G	0.0154538	0.0865337	intron-variant	LNX1	GRCh38.p7	4:53496831	TCCCAAAAATCTCCA[A/G]TTGAATTTTTCTCCC	84708
rs139720032	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53583151	TGTGCCATCAAACTC[C/T]TATGGCAATTTTATA	84708
rs139746863	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53491257	TGGTCACCTAAAAGG[C/T]TAGTTTTCAAAGTGA	84708
rs139778379	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53544639	CAGCACTGCTGCCCA[C/G]TACCATGCGAGAATC	84708
rs139808393	snp	A/C/T	0.00478244	0.0486902	intron-variant	LNX1	GRCh38.p7	4:53629973	AAGCCAAAATCTCCA[A/C/T]CTTGTACCTATACTA	84708
rs139830610	snp	C/T	0.00517822	0.0506191	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53510656	TTGCATTTGAGCGGC[C/T]CCAACGTAACAAATA	84708
rs139830703	snp	C/T	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53559912	AGCAATATTCCTGCC[C/T]CAACCTTCAAGTAGC	84708
rs139919946	in-del	-/CTAT	0.213635	0.247341	intron-variant	LNX1	GRCh38.p7	4:53477199	TTTTCTAAAGCACAG[-/CTAT]GCTATCGGTGTTTTA	84708
rs139929888	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53608878	AAACCAAATACCACA[C/T]GTTCTCACTTATAAG	84708
rs139953981	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53462283	AATCCTCAACTAAAA[C/T]AGCAAATGAGATTGA	84708
rs139954893	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53481512	CAGGTTTCAAAACTT[A/T]CCTGCACCTTCTTCT	84708
rs140022085	snp	A/G	0.0248432	0.108648	intron-variant	LNX1	GRCh38.p7	4:53572379	AGCATCTGGCTGAAC[A/G]TCTTGGGGAGAAAAA	84708
rs140054656	in-del	-/TAGGGAGAGTAG			intron-variant	LNX1	GRCh38.p7	4:53582087	GTCACTGTTAATTTT[-/TAGGGAGAGTAG]AGAAACCTAAGAATA	84708
rs140073966	snp	A/G	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53621429	TTTATTTTTCTCTGT[A/G]ATTTGCAGGATTCAA	84708
rs140079240	snp	A/G	0.00795532	0.062565	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53602814	CTGTACATCCATGAC[A/G]TATCATTTTACTCTA	84708
rs140079438	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53492328	CCTGAGGCAGAAATG[C/T]TTGAAGAGCACCAAG	84708
rs140083096	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53560944	CCATGGCTTCCTTGC[C/T]GGTAAACAGCCCTAA	84708
rs140091601	snp	C/T	0.00279162	0.0372561	intron-variant	LNX1	GRCh38.p7	4:53546879	AGACCGAGCCACTTG[C/T]GGAGGCAGAGCTGTG	84708
rs140094412	snp	A/C/G	0.000115318	0.00759261	synonymous-codon	LNX1	GRCh38.p7	4:53496206	TCCAAGCTGCTCCTC[A/C/G]GGGCTACTTTTGTTG	84708
rs140122571	snp	C/G	0.00517822	0.0506191	intron-variant	LNX1	GRCh38.p7	4:53563638	CTCCCAGGTTCAAGC[C/G]ATTCTCCTGCCTCAG	84708
rs140127345	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53499518	AGGGCATAAACTCTC[A/G]CTGTTCCATGGTTCT	84708
rs140141466	snp	A/G	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53630577	GGTGTTCCTAAGTGC[A/G]AGAAGGCTGTGATGT	84708
rs140168664	snp	A/G	0.00478085	0.0486577	intron-variant	LNX1	GRCh38.p7	4:53534911	CTTGTTGTAAAAATC[A/G]TTGAGTGAGGACCTG	84708
rs140269130	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53510853	CAAAGGTACAAGCCA[C/T]GGCTTTGTTGGGAGG	84708
rs140308406	snp	G/T	0.000153988	0.00877328	missense	LNX1	GRCh38.p7	4:53476799	GGGACCAGTCACTGG[G/T]TGGGGCCATGTTGTG	84708
rs140331986	in-del	-/A			intron-variant	LNX1	GRCh38.p7	4:53606481	ACAAACAAACAAAAA[-/A]CAAACAAAAAAAAAA	84708
rs140334180	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53645007	AATTCTTGCCAACAG[C/G]AGGAGAGTGAGCCCA	84708
rs140348387	snp	C/T	0.0182019	0.0936463	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53600047	ACCTTTTTAAAAAGG[C/T]CCCTCTCCCCAATAC	84708
rs140357471	snp	C/T	0.00914312	0.0669923	intron-variant	LNX1	GRCh38.p7	4:53527463	TTAGTCTCTACGAGC[C/T]TGGTGCTGACTCCTG	84708
rs140380940	snp	G/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53484925	CTTCTGATCTCCCCA[G/T]ACAAGGCTAATGTGC	84708
rs140440998	snp	G/T	0.000560058	0.0167247	missense	LNX1	GRCh38.p7	4:53496267	CTGTAGGCATCCGGG[G/T]CCTGTCCATTGTTCC	84708
rs140441599	snp	C/T	0.00993419	0.0697739	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53517803	TTATGAGCATTTTTG[C/T]GTAGTCAGAGGTGAA	84708
rs140464929	in-del	-/G	0.188	0.24219	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53512307	TCTTAAAAACACTGT[-/G]GTGGTCCAAACAAAA	84708
rs140473497	snp	A/G	0.0123036	0.0774623	intron-variant	LNX1	GRCh38.p7	4:53561547	GTATTTTTTCTTTCA[A/G]TAAAGTCTTCCCCAC	84708
rs140493707	snp	C/T	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53624394	TATAAGGGGAAACCC[C/T]TTTCACTTGGTTCTT	84708
rs140534002	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53582298	GTTACACTTGACAGA[A/G]ACACACAGGTGAACA	84708
rs140539343	snp	A/G	0.0115144	0.0749975	intron-variant	LNX1	GRCh38.p7	4:53616131	TTTTTAGATCCCACA[A/G]ATAAGTGAGAACATG	84708
rs140546259	snp	C/G	0.00119737	0.0244387	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53504204	AGATCTTCTGGAAAA[C/G]CTGCTGCAGCTTCTA	84708
rs140550729	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53512174	ACTTAAGGACACAGT[A/G]GCTGCTCCACCCTTC	84708
rs140570241	snp	G/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53620604	TGATGGGTACAACGT[G/T]CATTGCTCCACTGAT	84708
rs140579966	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53631082	GACCGCTGGGTCAAT[A/G]TAGAGAAGTGTGTGT	84708
rs140581525	snp	G/T	0.00914312	0.0669923	intron-variant	LNX1	GRCh38.p7	4:53530207	CCAAACATTCGTTAA[G/T]ATTATTTTTAAGTAA	84708
rs140611153	snp	C/T	0.00557542	0.0525036	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498160	ATTTTCAGGGAGGGC[C/T]GTAAGACTATAGGAA	84708
rs140611416	snp	C/T	0.0197687	0.0974348	intron-variant	LNX1	GRCh38.p7	4:53482293	AATGGCAGTAACTTG[C/T]CACTGCAGGAAGAGA	84708
rs140649246	in-del	-/T	0.00795532	0.062565	intron-variant	LNX1	GRCh38.p7	4:53463596	AATGTGAATGTTGGC[-/T]TTTTTTCCTATTCTG	84708
rs140659995	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53588833	ATTTGTGGTATCCCT[A/G]AAGGGCGAGACCCAG	84708
rs140679434	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53547198	TTATCTTTGCATGGC[A/G]TTATCAATTCTAAGA	84708
rs140694354	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53583500	AAGCCACTCATTAAT[A/G]AATCTGTGAATGACA	84708
rs140716226	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53645557	CACGTTGCAAAGAAC[G/T]GTTAATTATAATCTT	84708
rs140798396	snp	G/T	0.00636936	0.0560724	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53506183	CTTGGTTCTGCCATT[G/T]TTTAGCTGGGTGACT	84708
rs140838609	snp	C/T	0.00398564	0.0444627	intron-variant	LNX1	GRCh38.p7	4:53639868	GAAACCCTGTCTCTA[C/T]TAAAAATAAAAAAAA	84708
rs140845076	in-del	-/AT	0.0448719	0.142907	intron-variant	LNX1	GRCh38.p7	4:53465746	AAGTTAAAATGAAAA[-/AT]ATGTTGCTAGCTTTT	84708
rs140848626	snp	C/G	0.00676609	0.0577691	intron-variant	LNX1	GRCh38.p7	4:53536387	AAGTCGTTCCCTAAG[C/G]AACTCTTACAAAAAT	84708
rs140862102	snp	A/G	0.0130921	0.0798413	intron-variant	LNX1	GRCh38.p7	4:53527771	AGGGGAAAAGGGGCT[A/G]CCAGGGCTGTCAGCT	84708
rs140862181	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53551254	AGGTAGTTAGACAGA[C/T]ATGAGGCAGGGAAGG	84708
rs140911540	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53642139	AGATGGGAGGATTGC[C/T]TGAGCTCAAAAGGTT	84708
rs140956191	snp	A/C	0.000399281	0.0141238	intron-variant, nc-transcript-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53523214	TCCTGACAAAGAATA[A/C]GGATTGTTATGAAGA	84708
rs140967287	snp	A/G	0.00279162	0.0372561	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53521711	AGGGGGAAAGGAGGG[A/G]ATGCTTTTCCTGTTT	84708
rs140973009	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53638590	CTACTTAGTGCCCCG[C/T]TTTTCCTCATTTTTG	84708
rs140989232	snp	G/T	0.0126979	0.078662	intron-variant	LNX1	GRCh38.p7	4:53563949	TTGTGGAAATGTTGG[G/T]TTCAACCTACTTAGG	84708
rs140992277	snp	C/T	0.00676609	0.0577691	nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53604066	TGATAGTCATTCCAC[C/T]GCAACCTAAGGTCAC	84708
rs141014445	in-del	-/A			intron-variant	LNX1	GRCh38.p7	4:53542070	AATTACCTTGCACTC[-/A]GGGGGATGTCAGAAG	84708
rs141026198	snp	G/T	0.00159617	0.0282053	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519958	AACCGATGTGCTGGT[G/T]CTCACCCTATAAGTG	84708
rs141033971	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	LNX1	GRCh38.p7	4:53653472	ATGTATATGCAACAT[G/T]CAAGAAAGACACATA	84708
rs141038361	snp	G/T	0.0217236	0.101931	intron-variant	LNX1	GRCh38.p7	4:53552629	AGATCAGGAGTTCGA[G/T]ACCAGCCTGACCAAT	84708
rs141045704	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53483408	CTTTCTGCCACAGAT[C/T]AGTTTCACATGTGTC	84708
rs141071349	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53592450	CTGGCATCTTCCCAG[A/G]AGGGCTGTAAACATC	84708
rs141099044	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53466689	CACACCAGGAGATTA[C/T]ATCCCGCACCTGGCT	84708
rs141100556	snp	C/T	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53650218	CACAAATGCATAGCG[C/T]GTGTCACAGTCCTTA	84708
rs141120731	in-del	-/TC			intron-variant	LNX1	GRCh38.p7	4:53647375	TGTTTTAGGAAGCAA[-/TC]TCTCTCTCTCTTTTT	84708
rs141148300	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53532632	TTCTCCTCATGCCAG[C/T]TGGAAAATAACATTC	84708
rs141159009	snp	C/T	0.000395702	0.0140604	missense	LNX1	GRCh38.p7	4:53481841	ACGACGAGGTGAACA[C/T]GTCTTTCACTGGCCT	84708
rs141180496	snp	G/T	0.00517822	0.0506191	intron-variant	LNX1	GRCh38.p7	4:53490257	GCCTATGGAAAAAAG[G/T]CTTAAGAGGGACATT	84708
rs141236658	snp	A/G	0.000955251	0.0218338	missense	LNX1	GRCh38.p7	4:53478688	CGAGAGATTCACCGG[A/G]GTCTTTTTGGATATT	84708
rs141250443	snp	A/C/T	0.0287284	0.116357	intron-variant	LNX1	GRCh38.p7	4:53554591	GGGCACAGTGGCTCA[A/C/T]GCCTGTAATCCCAGC	84708
rs141255291	snp	A/G	0.00755907	0.0610114	intron-variant	LNX1	GRCh38.p7	4:53468175	AGCCAGAAGAGAGTG[A/G]GGGCCAATATTCAAC	84708
rs141305092	snp	A/G	0.00716266	0.059414	intron-variant	LNX1	GRCh38.p7	4:53484140	ATCTTTGACTTCTTG[A/G]CCTCCAGAACTGTGA	84708
rs141341676	snp	A/G	0.00597247	0.0543191	intron-variant	LNX1	GRCh38.p7	4:53626349	CCTCATATAATAAAT[A/G]TACTACAAAACAATG	84708
rs141362574	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53583846	GGGGTGCCATACTTG[A/G]GTTTGTTTGTAAAAA	84708
rs141365558	snp	A/C	0.0372196	0.131242	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53506680	ACCAACATGGAGAAA[A/C]CCCGTCTCTACTAAA	84708
rs141403212	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53623243	GAGTCTCACTCTGTC[A/G]CCCAGGCTGGAGTAC	84708
rs141405241	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53548998	ACAGAAGGAAATGAC[C/T]GACACTGGGGTCTAC	84708
rs141415300	snp	C/T	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53607465	AGAAATCAGAGATGA[C/T]GCAAACAAATGGAAA	84708
rs141450379	in-del	-/AT/ATAT			intron-variant	LNX1	GRCh38.p7	4:53652035	GAGAGAGAGAGAGAG[-/AT/ATAT]AGAGAGAGAGAGAGA	84708
rs141473202	in-del	-/TTTG	0.02016	0.0983543	intron-variant	LNX1	GRCh38.p7	4:53485634	TGCTCACAGGAAGAC[-/TTTG]TTTGATGTACTTTTG	84708
rs141475857	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53622716	TGAGAAAAACAAGAT[A/G]GCCCTAACACAGTGC	84708
rs141501251	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53634207	TTTCACAAGCCCAGT[G/T]GAATGGGCTGAGATA	84708
rs141528394	snp	C/T	0.00835141	0.0640778	intron-variant, synonymous-codon	LNX1, LOC101928879	GRCh38.p7	4:53576132	GCCCCTCCTTGATTC[C/T]GTGGCCCAGCAGCAG	84708
rs141528508	snp	G/T	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53593140	ACCTTTTACACTCAG[G/T]TGTTTCAGGAAAAGG	84708
rs141542711	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53637496	TTCCAAATGCTTTGC[A/G]CTACACCTGTCATTT	84708
rs141544843	snp	C/T	0.0154538	0.0865337	intron-variant	LNX1	GRCh38.p7	4:53561919	CGTTCTGTACGTGTA[C/T]CCCAGAATTAAAAAA	84708
rs141560605	in-del	-/A	0.164873	0.23506	intron-variant	LNX1	GRCh38.p7	4:53629222	TTGTCTGGATTGATT[-/A]GGGGGCTACCGAAAT	84708
rs141569891	snp	A/G	0.00159617	0.0282053	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53595816	GGCAATGAACCTACA[A/G]CGAAGACCATGCCTT	84708
rs141603317	snp	C/T	0.000231157	0.0107482	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507446	ATGATCTGCTTCTAA[C/T]AGTGGATCTCTCAAA	84708
rs141620414	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53583563	TACAGAAAAAAAAAA[A/C]CCTTTTAAATGGTCT	84708
rs141678192	in-del	-/AAAT	0.0821764	0.185298	utr-variant-3-prime, downstream-variant-500B	LNX1, FIP1L1	GRCh38.p7	4:53460358	ATCGGTGATGGTAAC[-/AAAT]AACATGGTATTTGAA	84708
rs141694542	snp	G/T	0.00318978	0.0398085	intron-variant	LNX1	GRCh38.p7	4:53636500	AGGGCTTGAGTGACC[G/T]TAAGCAAATCATTTC	84708
rs141705080	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53637654	TGCAACCTTATTTTT[C/T]GTGCCCACCCAGAAA	84708
rs141708035	snp	C/T	0.00795532	0.062565	intron-variant	LNX1	GRCh38.p7	4:53563160	GCAGTGAGCTGAGAT[C/T]GTGCCAGCCTGGGCG	84708
rs141724892	snp	A/G	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53590223	GACTGTCTGTCTAAG[A/G]CAAAAATGATCTCAG	84708
rs141726937	snp	C/T	0.00159617	0.0282053	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53514358	CCAATAAAGACATAC[C/T]CAAGACTGGGTAATT	84708
rs141739200	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53522129	GGCAGACGAGGCTTC[C/T]TGGGCTAGACAAGGC	84708
rs141746561	snp	C/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	LNX1, FIP1L1	GRCh38.p7	4:53462822	TCATTAAATTTCCTA[C/T]TGTAAAATATTTATC	84708
rs141776180	in-del	-/GT			intron-variant	LNX1	GRCh38.p7	4:53572787	CTGCCACCAGTGTGG[-/GT]GTGTGTGTGTGTGGG	84708
rs141798659	snp	C/T	0.0185938	0.0946107	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519127	GGCTGTCTCACTGCC[C/T]CTCTTCCTCTCCAAA	84708
rs141809459	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53633509	TACTGATCCTTGTTC[C/T]GTGGGCTATGGCCAG	84708
rs141828494	snp	A/G	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53584998	TCTTTGGTTCTTCCA[A/G]TTGTCTTCCTGGGTA	84708
rs141843535	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53571946	GATTACAGGTGTGAG[A/C]CACTGCGCCCAGCAA	84708
rs141847770	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53544489	GTGAGCCACCATGTC[C/T]GGCCTGAGAGGTGCT	84708
rs141863224	snp	C/T	0.0221141	0.102801	intron-variant	LNX1	GRCh38.p7	4:53474449	TTGCCACAGAGACTG[C/T]GTGGCCCTCAAAGCC	84708
rs141918725	snp	A/G	0.00358779	0.0422022	intron-variant	LNX1	GRCh38.p7	4:53650652	CTAGCTCTTTTCACC[A/G]TTCTATACTACCGCC	84708
rs141936072	snp	A/G	0.00279162	0.0372561	intron-variant, utr-variant-3-prime	LNX1, LOC101928879	GRCh38.p7	4:53577221	ATGGGCCATGCAAAA[A/G]ATTATCATCTACAAT	84708
rs141946274	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53641784	ATCAAACATTGTGTA[C/T]TCTTTTTGGTGTCTG	84708
rs141948592	snp	A/G	0.0115144	0.0749975	intron-variant	LNX1	GRCh38.p7	4:53610140	TTTTCATATGTCCGC[A/G]GAACATTTATAGAGA	84708
rs141949006	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53537294	CTTTCAAATGGTAAA[C/T]AACACCCTTGAAGTC	84708
rs141957672	snp	C/T			upstream-variant-2KB	LNX1	GRCh38.p7	4:53654015	CTTGGATTTGTTTGG[C/T]GACGCTTTGGGGGTA	84708
rs141959810	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53538389	AGCTTTCCCTGTGAA[G/T]TTCTGCTGTATTTGG	84708
rs141975035	snp	C/T	0.0134861	0.0810011	intron-variant	LNX1	GRCh38.p7	4:53580795	TCCTTAGAACCATTG[C/T]TATCTGAGGAATGTG	84708
rs141985449	snp	A/G	0.0170251	0.090679	intron-variant	LNX1	GRCh38.p7	4:53613968	CACAACCTCACCAGC[A/G]TCTGTTATTTTTTGA	84708
rs141985747	snp	G/T	0.00398564	0.0444627	intron-variant	LNX1	GRCh38.p7	4:53543163	ACCACGTCTGTCCTG[G/T]GTGCTACTGTTATCC	84708
rs141991617	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53488751	CAGAGCAGCCCACCC[C/T]TGAGACCACATGATG	84708
rs142047741	snp	C/T	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53587637	TCGAGTAGTCAAGAT[C/T]GTATCCTGGTCAAGA	84708
rs142056076	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53473371	AAAACATGCAGCACT[A/G]TTTACAATAGCAAAG	84708
rs142078107	snp	C/T	0.433963	0.169285	intron-variant	LNX1	GRCh38.p7	4:53471071	AAGCTGGAGGCATCG[C/T]ACTACCTGACTTCAA	84708
rs142116740	snp	A/G	0.00636936	0.0560724	utr-variant-5-prime, upstream-variant-2KB	LNX1	GRCh38.p7	4:53652462	CATGCATTAGCATCA[A/G]TGACAAATCTCTTCT	84708
rs142168503	snp	A/G	0.0142736	0.0832652	intron-variant	LNX1	GRCh38.p7	4:53613555	GCATTGTTCCAATGC[A/G]GTATTTGGTTTTCTG	84708
rs142170657	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53541864	CAGATAGCTTTGTAA[A/T]AAGTGAAATTTGGAG	84708
rs142190654	snp	C/G	8.27959e-05	0.00643359	synonymous-codon, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498668	GTCTCCTGGCAGTAG[C/G]CGGCCGTCTCTGGCG	84708
rs142201649	snp	C/T	0.00358779	0.0422022	intron-variant	LNX1	GRCh38.p7	4:53540082	TAGCAACTACCCCAT[C/T]CTTGCTAACAACTCC	84708
rs142259886	snp	A/C	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53637727	TACATAAACCAAAAC[A/C]CAGCCAGTTTCTGAG	84708
rs142320407	snp	C/T	4.94222e-05	0.00497078	missense	LNX1	GRCh38.p7	4:53496246	TGAAAGCTGTCATCT[C/T]GGGGTCTGTAGGCAT	84708
rs142321173	snp	C/T	0.00159617	0.0282053	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53594774	TATAGTGCAGTGGTG[C/T]CATCATGGCTCACTG	84708
rs142330087	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53631498	TTTTCCTCTTCCTAG[C/G]ACACTGATCCCAATA	84708
rs142338961	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53559066	TTAATAGAAATGGCT[A/C]GAAGGGATAATTACA	84708
rs142358903	snp	C/T	0.0263992	0.111815	intron-variant	LNX1	GRCh38.p7	4:53561403	CAGCTAATTTTTCTA[C/T]TTTTAGTAGAGATGG	84708
rs142360009	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53596866	TAGATCTTGTTATCA[C/T]CCCAAAATCTCCCAT	84708
rs142370075	snp	C/T	0.0134861	0.0810011	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53599789	TCTATGTATGTCACC[C/T]GAGAAAACCTATACC	84708
rs142376028	snp	C/G	0.00318978	0.0398085	intron-variant	LNX1	GRCh38.p7	4:53492440	GCCACAAGACGTATG[C/G]CATTGCAGGCCATAG	84708
rs142387120	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53630899	TTGCATCAGCTTTTA[G/T]AATTTGGGAAGGGGA	84708
rs142388156	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53557796	AAAATGGATATATCA[G/T]CTAGGGAATGGACTC	84708
rs142407662	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53511189	CTCATACTGTGTAAT[A/G]TTAGCTTTCTCCAGT	84708
rs142431172	snp	G/T	0.00716266	0.059414	intron-variant	LNX1	GRCh38.p7	4:53485747	GAGAAACATCCCCTA[G/T]CACCAGAGAATCTTT	84708
rs142450551	snp	A/G	4.94205e-05	0.0049707	synonymous-codon	LNX1	GRCh38.p7	4:53476878	CTCTTTGACTTCCAA[A/G]GCTTTGAGTACTATC	84708
rs142478177	snp	C/T	0.0414363	0.137845	intron-variant	LNX1	GRCh38.p7	4:53567692	AAACCCTTCAAAAAA[C/T]TGATGAATCCAGGAG	84708
rs142518564	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53505805	TAAAAAGGGGGCTGA[A/G]GGAGTGAGGTTTCCA	84708
rs142543865	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53561736	TCTTGGGCCAATTAC[A/G]TCACGTTTTCATTCA	84708
rs142558891	snp	C/G	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53477810	AGAAAGGCCTTGAGT[C/G]CTTTCTGACCCGAAA	84708
rs142604643	snp	A/G	0.0221141	0.102801	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53517376	GATAAAAATAAATGC[A/G]TCAGTCAGCGCCTTC	84708
rs142621826	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53578500	GGTACAGTAAAAACA[A/G]TATTTTAATCTTATG	84708
rs142672720	snp	A/G	0.000153988	0.00877328	synonymous-codon	LNX1	GRCh38.p7	4:53476809	ACTGGGTGGGGCCAT[A/G]TTGTGGTTGGAGTCC	84708
rs142693119	snp	C/T	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53528587	GCTTTATCACAGTTA[C/T]GTACATGTAGGAGAA	84708
rs142709000	snp	A/C	0.0130921	0.0798413	intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53559612	GCAATGCCCATAAAC[A/C]ACAAAGGGCTTAACG	84708
rs142734822	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53612873	CTGGTTGACAGAGTG[A/G]GACCCCATTTCAAAA	84708
rs142772194	snp	A/G	0.00676609	0.0577691	intron-variant	LNX1	GRCh38.p7	4:53616619	TTTCCAGTTGTTGGT[A/G]GACTGAGCTTATTGG	84708
rs142773441	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53645992	ACTTATAAAGGAATT[C/G]CTTTATTTATTCCTT	84708
rs142809991	snp	C/T	0.00478085	0.0486577	intron-variant	LNX1	GRCh38.p7	4:53632176	CTGCCTGAGGCTGGC[C/T]GCTGCGGTGGCCAGG	84708
rs142810080	snp	A/G	0.00835141	0.0640778	intron-variant	LNX1	GRCh38.p7	4:53585998	AAAATATTTGGAGAC[A/G]GCAGCCACATAGATT	84708
rs142817216	snp	C/T	0.00159617	0.0282053	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508952	CTATAAAAAAAAATC[C/T]AGAAAACTCCACAAA	84708
rs142885651	snp	C/G/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53639215	AGGCCATTCTTCTCA[C/G/T]TGAATTATCACAGGA	84708
rs142904350	snp	C/G	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53591884	GTAATTTAGCAGACA[C/G]AAAAAGGAAGAGTGT	84708
rs142912744	snp	A/T	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53516777	GCCAGTCCATCTACC[A/T]ACTTCTGGGGTTCAG	84708
rs142927302	snp	A/G	0.00716266	0.059414	intron-variant	LNX1	GRCh38.p7	4:53624450	TAAGACATGTCTTTC[A/G]CCATCTGCCATGATT	84708
rs142947795	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53501421	TCAGACCAAGAAGCT[A/G]GGAGTACAGGTGTGT	84708
rs142988224	snp	A/G	0.00874735	0.0655527	intron-variant	LNX1	GRCh38.p7	4:53635750	TTAGCCTATAATCTC[A/G]GCACTCCCAGGTTTT	84708
rs142996124	snp	C/T	0.00795532	0.062565	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53462129	ATAGAGAAGCATGCA[C/T]GCATAAAGTGAATGG	84708
rs142998694	snp	C/T	0.00398564	0.0444627	intron-variant	LNX1	GRCh38.p7	4:53529640	CACGGCATCTGACAG[C/T]TCCATGTACATTGTG	84708
rs143011902	snp	A/C	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53495831	TTACAGGCATGGGCC[A/C]CCACGCCCAGCCGAG	84708
rs143067453	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53513719	GCCACCATACTGGTC[C/T]AAGCCACCATCATCA	84708
rs143086522	snp	C/T	0.00358779	0.0422022	intron-variant	LNX1	GRCh38.p7	4:53641686	TCTCCCTCTCACTCC[C/T]CATTCACCAGGTCCC	84708
rs143108165	snp	A/G	0.00199481	0.0315187	intron-variant, utr-variant-3-prime	LNX1, LOC101928879	GRCh38.p7	4:53576793	TGGAAACAGCCCAGC[A/G]GTCATAAACTGTATT	84708
rs143110665	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53593888	AGAAACTGCCTAAGG[A/G]CAAGCTCATCGGCAA	84708
rs143112697	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53518319	CATGAGACACACTGG[C/T]TAGTCTCTGCACAGT	84708
rs143139952	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53510683	AATACTTGAATGAAA[C/T]ACTTCCAGGCAGGCT	84708
rs143155722	snp	C/G	0.0142736	0.0832652	intron-variant	LNX1	GRCh38.p7	4:53590083	TGGCCAAACCCCCCC[C/G]CTTAAACTCACAAGC	84708
rs143180000	snp	A/T	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53649891	TGTTCCACCCTAGCC[A/T]AGCACCTGGAACCTC	84708
rs143181790	snp	A/T	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53646871	CACTATTATTTCATT[A/T]TTGTTCCAATTTAAC	84708
rs143197560	snp	A/C	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53637251	AGAAACTTGTGTTTT[A/C]CTTTCTTCACAGCTG	84708
rs143199807	snp	C/T	0.000399281	0.0141238	nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53604142	ATTTAATCAAATTGA[C/T]GACAATTTGAAGTTG	84708
rs143207058	snp	C/G	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53531220	TTTGTCTAGCAGGAA[C/G]TGCTGTGGACATGAG	84708
rs143216294	snp	A/C	0.0123036	0.0774623	intron-variant	LNX1	GRCh38.p7	4:53589819	TCTGACTCTGAATTC[A/C]AGTCTTTGTCACTTC	84708
rs143221927	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53602258	GATGCCAAGACGAAA[C/T]TAAATATGCAGGGAC	84708
rs143228088	snp	A/C	0.0123036	0.0774623	intron-variant	LNX1	GRCh38.p7	4:53475172	TTTGGAGCAAAAAGC[A/C]CCTCACATTGTCCTC	84708
rs143228724	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53528793	CCATCTCCCTGGAAG[G/T]TGGGGACTAGCTGGG	84708
rs143241829	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461659	GGGAATACTTACTGT[A/G]ACTCATCCTCCATTC	84708
rs143266799	snp	A/G	0.0189856	0.0955633	intron-variant	LNX1	GRCh38.p7	4:53625797	AGGTAACAGAGCAAG[A/G]TCCTGTCTCAAAATG	84708
rs143307492	snp	A/G	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53630208	AATTAACAGCAAGTC[A/G]TTAAAATGTTTTGTT	84708
rs143311709	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53556614	AAAAGCTTCTGCAAG[A/G]TCATTATTTCCTCAG	84708
rs143350032	snp	G/T	0.0111196	0.0737302	intron-variant	LNX1	GRCh38.p7	4:53642454	GGCCTAGGACAAAGG[G/T]TCTCCTGGCCATTGA	84708
rs143391695	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53548532	GGAGATATTTCTCCA[C/G]TCTCTTAAAGTTCTC	84708
rs143409896	snp	A/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53484642	TCTGACACTAACCAG[A/T]CCAAATCTTCATGAC	84708
rs143471257	snp	A/G	0.00279162	0.0372561	intron-variant	LNX1	GRCh38.p7	4:53533425	TTTATTTGAGGTGGC[A/G]TCTCCCTCTGTCGCC	84708
rs143475085	snp	A/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53479556	GCAATGGAAAAAGAA[A/T]ATCATCTGTGAAAGC	84708
rs143491569	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53615914	TTATAAACAATCCAA[C/T]CATACTATTCTAGTT	84708
rs143497847	snp	C/G	6.59033e-05	0.00573997	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507384	GGCAACTGCACTCCC[C/G]CTCTTTGTCCTTCGA	84708
rs143518303	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53495222	ATTATCTCAAAATAC[A/G]AAGGTGAGTTACAAT	84708
rs143525182	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53632491	AGTCAGACAATGATC[A/G]ACTGACTAGGGTACA	84708
rs143567270	snp	A/G	0.00398564	0.0444627	intron-variant	LNX1	GRCh38.p7	4:53529895	GCTTCTCTATTCCAA[A/G]ACATGTACAGAGAAC	84708
rs143573829	snp	C/T	9.89315e-05	0.00703249	missense	LNX1	GRCh38.p7	4:53476753	TGTGTTTGGACTTAC[C/T]GTGGTAATTCCAGCC	84708
rs143600488	snp	A/G/T	6.61238e-05	0.00574962	synonymous-codon	LNX1	GRCh38.p7	4:53478740	AATTGTAGGATGGAG[A/G/T]GGCTGAAGGCACAGA	84708
rs143601532	snp	C/T	0.0655868	0.168795	intron-variant	LNX1	GRCh38.p7	4:53609836	AATTTCTACATAATG[C/T]TATATAAATAAATCA	84708
rs143608926	snp	A/G	0.00438332	0.0466095	intron-variant	LNX1	GRCh38.p7	4:53535157	TTTTAAGGAACACAA[A/G]GGATGTAATCAAAGT	84708
rs143622691	snp	C/T	0.0267878	0.112589	intron-variant	LNX1	GRCh38.p7	4:53570753	AATCTTTTGGCTGGG[C/T]GTGGTGGCTCACGCC	84708
rs143625072	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53488404	CAGGTCAACTATTCC[C/T]AGTTTTTTCCACATT	84708
rs143640303	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53521621	TGAGCTTCCTCTTCC[A/C]TCCCAATATATTTAA	84708
rs143640763	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53624189	ACTCTTTTATACCTT[C/T]CCAATCATTAGCCTA	84708
rs143648692	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53549522	GATTGTATTTAGCTC[A/G]TGATTCACACAAACT	84708
rs143659476	snp	C/T	9.92113e-05	0.00704243	synonymous-codon, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508221	GTAGTGGGAGGCACC[C/T]TTACAGCTGTAACAG	84708
rs143693465	snp	C/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53644758	GAGACTGGGAGGTTC[C/G]TGCTGGAGGGAGCTC	84708
rs143736534	snp	C/T	0.00279162	0.0372561	intron-variant	LNX1	GRCh38.p7	4:53648482	GTTGAACTGTAGGGG[C/T]TCTTTACATATTCTG	84708
rs143740978	snp	A/G	0.00318978	0.0398085	intron-variant	LNX1	GRCh38.p7	4:53572415	TCACTGACATAATGA[A/G]CGTGGAAAACATGTG	84708
rs143771450	snp	C/G	0.00398564	0.0444627	intron-variant	LNX1	GRCh38.p7	4:53466514	TGGGTGCAGCACACC[C/G]AGCACGAGCCAAAGC	84708
rs143801332	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53588157	ATTTCAATTATTCCT[C/T]CCAACAGCTCTGAGT	84708
rs143827192	snp	A/G	0.0256215	0.110247	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508507	AAATTTATTCAGGTC[A/G]CCATGGTGTCTACAT	84708
rs143854890	snp	C/T	0.0189856	0.0955633	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53522358	TTTATTCCACAAATA[C/T]TGAAGTGATTACTAA	84708
rs143887483	snp	C/T	0.0023933	0.0345097	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53503485	TGGGTAACTAGGATG[C/T]ATTATCAATGAGTAG	84708
rs143890609	snp	C/T	0.00318978	0.0398085	intron-variant	LNX1	GRCh38.p7	4:53554242	GGACTCTCTCCCCTA[C/T]ATGTAAGTCCCCAGT	84708
rs143905652	snp	C/G/T	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53629278	CCCTGTCTCCAGCCA[C/G/T]CCCTGGGTGCATCCA	84708
rs143933941	snp	C/T	0.00478085	0.0486577	intron-variant	LNX1	GRCh38.p7	4:53628312	AATACAAAACAATCC[C/T]ATCAAAAAGTAGGCA	84708
rs143972844	snp	A/G	0.00716266	0.059414	intron-variant	LNX1	GRCh38.p7	4:53606468	CCAGAAAAAACAAAC[A/G]AACAAACAAAAAACA	84708
rs143977596	snp	C/T	0.00478085	0.0486577	intron-variant	LNX1	GRCh38.p7	4:53550445	AAATCCAGGGATCAG[C/T]AACACTTTTTTTTCC	84708
rs143979542	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53465610	TCCAATTCACCAACA[A/G]TGTAAACTTCCTTAG	84708
rs143993695	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53555355	TTCCTCTTTCTACCC[A/G]TTTCTGCCTCATTCC	84708
rs144074631	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53648884	TGTCAGGACAATCAT[A/G]ACAATCACTATTGCC	84708
rs144099794	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53566178	CCTGGAGAAGAGCAA[A/C]TCCAAGACACATAAT	84708
rs144125909	snp	C/T	0.00795532	0.062565	intron-variant	LNX1	GRCh38.p7	4:53586915	TTAATCTAAAATAAT[C/T]CTATGAGATCATTAA	84708
rs144132490	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53510644	ATAAAAGCCAACTTG[C/G]ATTTGAGCGGCTCCA	84708
rs144168008	snp	C/G	0.00914312	0.0669923	intron-variant	LNX1	GRCh38.p7	4:53614016	TAGCCGTTCTGACTG[C/G]TGTGAGATGGTATCT	84708
rs144193893	snp	A/G	0.0228947	0.104514	intron-variant	LNX1	GRCh38.p7	4:53486293	CCCAATCGGCAGAGC[A/G]CACTACAGCCCCAGA	84708
rs144214359	snp	G/T	0.0197687	0.0974348	intron-variant	LNX1	GRCh38.p7	4:53491626	CAGATTTGGTGCTTC[G/T]TTGGTAAATGGTTTG	84708
rs144220715	in-del	-/GA	0.164219	0.234823	intron-variant	LNX1	GRCh38.p7	4:53644388	CCTGGGCAACAGAGT[-/GA]TGAGAGTCTATCTCA	84708
rs144252061	in-del	-/AA	0.395635	0.2032	intron-variant	LNX1	GRCh38.p7	4:53606487	AAACAAAAAACAAAC[-/AA]AAAAAAAACAGAACA	84708
rs144277700	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53582284	TGCTTCAGCTGATTG[A/T]TACACTTGACAGAGA	84708
rs144286823	snp	C/T	0.000399281	0.0141238	nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53603780	TCACCTCCCACCAGG[C/T]CCCAACTCCGACACT	84708
rs144288492	snp	C/T	0.00318978	0.0398085	intron-variant	LNX1	GRCh38.p7	4:53651020	TACCATCATTCTCAT[C/T]TTACATATTGGCAAG	84708
rs144296938	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53541274	TTAGCAACTGAATCA[A/T]CTTCAGCAAATGGCT	84708
rs144302447	snp	A/G	0.000115322	0.00759261	synonymous-codon	LNX1	GRCh38.p7	4:53478662	TGATGCTCCCCCTGC[A/G]ACGGTCATGCCGAGA	84708
rs144318358	snp	A/T	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53485271	TTGGGGAAACTCCGA[A/T]GTTTTGAAGGATCCC	84708
rs144331117	snp	A/C	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53608223	AAACTGTGCATCCTA[A/C]AAATGTCTAATATCC	84708
rs144345559	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53536233	CATATTCTCAGGTCA[A/G]TCTCTTAGTGGAAAT	84708
rs144358287	in-del	-/A			intron-variant	LNX1	GRCh38.p7	4:53628797	ATACTACTCAGCCAT[-/A]AAAAGAAATGAAATA	84708
rs144380065	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53582471	GTCAAGTAATAAAGA[A/G]TTCTCTCCAGCAAGG	84708
rs144383546	snp	G/T	0.00874735	0.0655527	intron-variant	LNX1	GRCh38.p7	4:53650627	AGCTGGGATTCAAAA[G/T]TAGATCTGTCTAGCT	84708
rs144391746	snp	A/G	0.00279162	0.0372561	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53504489	TATCCAGGTTACTCA[A/G]ACTTTCTCCATATCA	84708
rs144403182	snp	C/T	0.00676609	0.0577691	intron-variant	LNX1	GRCh38.p7	4:53551569	TAAACACACTGCGCA[C/T]GCTCACCCCCCAAGT	84708
rs144424207	snp	A/G	0.00105435	0.022936	synonymous-codon	LNX1	GRCh38.p7	4:53478602	GCTTATGACTCCTCC[A/G]GGCTCAACACTGATG	84708
rs144506643	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53601994	CTGACTTCTCCAGTC[A/G]GCACCATTGTCCTCC	84708
rs144512754	snp	A/T	0.0111196	0.0737302	intron-variant	LNX1	GRCh38.p7	4:53620689	TTGCACTTGTACCCC[A/T]TGAATATATAAAAAT	84708
rs144577115	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53636435	ATCTTTGGGACTCTG[A/G]TGAGACATTCTTGTC	84708
rs144588444	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53624552	AGGTGTGTCTTTATC[A/G]GCAGCATGAAAATGG	84708
rs144600422	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53550081	CAAAGGGGGGAAAAA[A/G]TAAAATCATGAAACA	84708
rs144716642	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53506263	GGGAATGATAGTCCT[A/G]TCCCCTTAACATTAT	84708
rs144738661	snp	A/G	0.0543475	0.155628	intron-variant	LNX1	GRCh38.p7	4:53564785	CAGGTCAGTGGGTGC[A/G]CGCACCCTGCGCCAG	84708
rs144748793	snp	C/G	0.00676609	0.0577691	intron-variant	LNX1	GRCh38.p7	4:53496885	CCAGTCCTCACCACT[C/G]TGTGTGTATGTAGAT	84708
rs144777706	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53522020	GGCTGGTCTTGAATT[A/T]CTAGGCACAAGCAAT	84708
rs144794824	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53598286	TGCCCAGGCTGGAGT[A/G]CAGTGGCACAATCAC	84708
rs144812809	snp	A/G	0.0154538	0.0865337	intron-variant	LNX1	GRCh38.p7	4:53634897	GGCTGGAGTGCAATC[A/G]TGGGATCGTAGCTCA	84708
rs144839849	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53473889	ATGAAATATAAAATA[C/T]ATCAAAGAAACAAAT	84708
rs144851600	snp	A/G	0.00398564	0.0444627	intron-variant	LNX1	GRCh38.p7	4:53571724	CTGGAGTGCAGTAGC[A/G]CATCACAGCTCACTT	84708
rs144860514	in-del	-/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53518811	GGCAACTGTAACATG[-/G]GGACGTAGGGAAAAG	84708
rs144909612	snp	C/T	0.0103295	0.0711199	intron-variant	LNX1	GRCh38.p7	4:53561875	AGCAAACCATCATGA[C/T]ACACATACACCTATG	84708
rs144922620	snp	A/T	0.0225045	0.103662	intron-variant	LNX1	GRCh38.p7	4:53638652	GGCCCCGAAGCATAA[A/T]GCTGAAGTGCTGCCA	84708
rs144932510	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53621992	GCACAAACAATTCTC[A/G]TATACATTGGTGCAG	84708
rs144943429	snp	A/G	0.00358779	0.0422022	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53515973	TTCGCACAAAAGGCC[A/G]AGTGTGGTGGCTCAT	84708
rs144948760	in-del	-/TTTTTA	0.201717	0.245293	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53600711	TGGACGGCCTCTGTT[-/TTTTTA]TTTTTATTTTTATTT	84708
rs144950563	snp	G/T	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53579720	ACTCATCAGAACAAT[G/T]GGATCCTTGGTGTGC	84708
rs144958465	snp	C/T	0.00438332	0.0466095	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53499757	GTTCTTTCTACCAGA[C/T]ATTGTTGTTAACAAA	84708
rs144972515	snp	A/G	0.00755907	0.0610114	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53520055	CTTTGTGGATGTTCT[A/G]TCCCCACGTTTAGTA	84708
rs144976944	snp	C/T	0.00597247	0.0543191	intron-variant	LNX1	GRCh38.p7	4:53530856	GAAAAAAGGAGGGGG[C/T]ACAGGGAATTAAAAT	84708
rs144986746	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime	LNX1	GRCh38.p7	4:53652228	AGATAGTCCGTTTGA[A/G]AGCTGAGCTTTTCTG	84708
rs145074923	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53526963	ATGCTAAAGCAATAG[A/G]AATGAAACACCTAAA	84708
rs145092359	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53583882	TAACAGAAAAGATGT[C/G]CTTCCATTTCCTAGT	84708
rs145095316	snp	A/C/G	0.0197687	0.0974348	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53506798	GAGGCAGAGGTTGCA[A/C/G]TGAGCCGAGATCATG	84708
rs145145208	snp	C/T	0.00597247	0.0543191	intron-variant	LNX1	GRCh38.p7	4:53525790	ACAGTATCTCCCTTT[C/T]AGGGAGGGCACTCTG	84708
rs145158033	snp	A/G	0.00358779	0.0422022	intron-variant	LNX1	GRCh38.p7	4:53622932	ATTATTCTTCTGGAG[A/G]AGAGTTTTAATGAGT	84708
rs145178075	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53626390	TTTAAAAGGGTAAAT[A/T]TTAGGTATGTGAATT	84708
rs145178533	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53580272	GCCTAACTTTTTAAG[A/T]CCTTTAATTATTTGA	84708
rs145181591	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53501746	GCTGAAGCAATGAGG[A/C]CCTCTGGCCATTTTG	84708
rs145209772	snp	C/T	0.0111196	0.0737302	intron-variant	LNX1	GRCh38.p7	4:53619937	GTCAGCTGGTGTTCT[C/T]ACTAATTAAGAACAA	84708
rs145209844	snp	C/T	0.00358779	0.0422022	intron-variant	LNX1	GRCh38.p7	4:53545928	TTCTCCCGCCTCAAC[C/T]TCCTGAGTAGCTGGT	84708
rs145212335	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53631370	CAGCAGAAAGAGACC[C/T]GCTAAAGAAGACCTG	84708
rs145254515	snp	A/T	0.0205511	0.0992634	intron-variant	LNX1	GRCh38.p7	4:53497333	GAGGAGAAATAACTT[A/T]CTTGAATTTCTGTAG	84708
rs145317292	snp	A/G	0.00517822	0.0506191	intron-variant	LNX1	GRCh38.p7	4:53542194	AGCTTGAAAAATTGG[A/G]AATAACTATTAGGAA	84708
rs145332459	snp	C/T	0.0154538	0.0865337	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53595925	GATTGAATGCCACAA[C/T]TAAAATGGACATATT	84708
rs145352117	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53598996	TTGCTTAACAGAGGA[A/G]TGTTACAGATGCAGT	84708
rs145391591	snp	A/G	0.00795532	0.062565	intron-variant	LNX1	GRCh38.p7	4:53589289	GCCTGTGAGGCTAGC[A/G]GAGACAAATCTGCCC	84708
rs145399112	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53464493	TCAACATGAAAAAGA[A/T]GTTTATGGGAGATTA	84708
rs145407071	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53600762	TTGAGACAGAGTCTC[A/G]CTCTGTTGCCAAGGC	84708
rs145425393	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53527758	AGTGAGCCTCAGCAG[A/G]GGAAAAGGGGCTACC	84708
rs145462345	in-del	-/G			intron-variant	LNX1	GRCh38.p7	4:53497753	TGCCCCGAGGGCCCT[-/G]GTCTTATGCTCCACC	84708
rs145503218	snp	A/G	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53557213	TTTCAGAGATGCACA[A/G]TGATGTATTTAGGGG	84708
rs145510342	snp	C/G	0.310386	0.242597	intron-variant	LNX1	GRCh38.p7	4:53470310	CATGCTAAAAACTCT[C/G]AATAAATTAGGTATT	84708
rs145540693	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53480309	TAAGACATATGACAG[A/G]GGGTTGCAGCAGAAA	84708
rs145553772	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53640184	TTGTTCCCATTTCCA[A/G]TTGTTGGCATTTCTT	84708
rs145581170	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53645024	GGAGAGTGAGCCCAG[A/G]AAATCTCCAGACAGC	84708
rs145593080	snp	A/G	0.0107246	0.0724382	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53596537	ATTACACATATTTTT[A/G]TGTTTCTATGATCTC	84708
rs145599611	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53522151	AGACAAGGCTTCTTG[C/T]AGTCAGACACATTGA	84708
rs145636095	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53609168	TGGGGAAAGGACTCC[C/T]GATGTTTATTACCTG	84708
rs145640428	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53536632	TTTCCATATTGCTTC[C/T]TCATAAAAAGTTTTG	84708
rs145652095	snp	C/T	0.00597247	0.0543191	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53504715	TGGCTCTTCCTTTCA[C/T]TTGAATACTCAAAGG	84708
rs145684663	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53482136	ATCAGATATTGCTAA[C/T]TCATTTTTAATTAAT	84708
rs145700645	snp	A/T	0.000153988	0.00877328	synonymous-codon	LNX1	GRCh38.p7	4:53478704	GTCTTTTTGGATATT[A/T]ACCACCTTCTCATGA	84708
rs145707110	in-del	-/ACTTT	0.108048	0.20579	upstream-variant-2KB	LNX1	GRCh38.p7	4:53652856	CAATACCTTGCCAAA[-/ACTTT]CAAAGATTTTCTATT	84708
rs145708153	snp	C/T	0.00716266	0.059414	intron-variant	LNX1	GRCh38.p7	4:53561165	ATGAGATGCTTAGTC[C/T]GGCTAAAATGACCAG	84708
rs145730929	snp	C/T	0.253824	0.249971	intron-variant	LNX1	GRCh38.p7	4:53570983	GGTGAGCAGAGATCG[C/T]GCCACTGCACTCCAA	84708
rs145733237	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53564255	TGAAATTCCCAGTCT[C/G]CTTCAGGCAGCTGAG	84708
rs145739859	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53482713	AGAAAAGGGGAGGGT[A/G]AGTGGGGTGAGGGAT	84708
rs145741011	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53489162	CATGCTGAAGAGGTG[A/G]TAGCTCCTTCAATGA	84708
rs145752200	snp	A/G	0.0119091	0.0762411	intron-variant	LNX1	GRCh38.p7	4:53622650	TAAATATAACAAAGG[A/G]GGAAGTTCATGAGAT	84708
rs145760212	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53547251	TTAAGAAGTATGTCT[C/T]AGAATTGATGAAATA	84708
rs145765753	snp	C/G	0.000798403	0.0199641	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53603226	TGGTTGCAGGGCTTC[C/G]TTGGGAGCCGACTCC	84708
rs145771836	snp	C/T	0.00318978	0.0398085	intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53574767	TCACAGGCTACTTCA[C/T]AGAACTCTTGTGAGG	84708
rs145775437	snp	C/T	0.0123036	0.0774623	intron-variant	LNX1	GRCh38.p7	4:53493215	CTCATGATCTGCCTG[C/T]CTCGGCCTCCCAAAG	84708
rs145790322	snp	G/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53560698	ATTTGAGACCATGAG[G/T]TGACAAACTTGAGGA	84708
rs145799275	snp	A/G	0.0023933	0.0345097	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53500556	CCTAATGAATTAATA[A/G]GTACTCAACTCTCTA	84708
rs145852429	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53626859	CTAATAAAAACCACA[C/T]CATGCACCCATCTGT	84708
rs145862081	snp	A/T	0.0138799	0.0821421	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53605649	TATTCATGTTTTTTT[A/T]AAAATTCCATATATA	84708
rs145875378	snp	C/G/T	6.79548e-05	0.00582867	missense	LNX1	GRCh38.p7	4:53481827	GAACCTGGCGGGACA[C/G/T]GACGAGGTGAACACG	84708
rs145898168	snp	A/G	0.00318978	0.0398085	intron-variant	LNX1	GRCh38.p7	4:53610178	GGTACCTGACTACAA[A/G]GAAAACTTGAGCAAA	84708
rs145907043	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53616428	TATGTTGACCAGATT[A/G]TCTCATGTGACACCT	84708
rs145914450	snp	G/T	0.0236746	0.106192	intron-variant	LNX1	GRCh38.p7	4:53544370	GGCTAATTTTCTGCA[G/T]TTTTAGTAAAGACAG	84708
rs145916448	snp	A/G	0.000115375	0.00759437	synonymous-codon, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498695	GGCGATCACCCCATC[A/G]CGATAAATGTGTTGG	84708
rs145922655	snp	C/T	0.0154538	0.0865337	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53597393	TTTGCAAGCACAGAA[C/T]GCCACCACCTGCCAG	84708
rs145929273	snp	A/C	0.0193772	0.0965046	intron-variant	LNX1	GRCh38.p7	4:53469336	TCTGGGACACATTCA[A/C]AGCAGTGTGTAAAGG	84708
rs145945720	in-del	-/TTG	0.159622	0.233092	intron-variant	LNX1	GRCh38.p7	4:53534897	CCTGTCTTAACAGCC[-/TTG]TTGTAAAAATCGTTG	84708
rs146013750	in-del	-/TTC			intron-variant, downstream-variant-500B, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53459960	GATGGCTTTTCAATA[-/TTC]TTCTAAATTTGGGTT	84708
rs146022876	in-del	-/T			intron-variant	LNX1	GRCh38.p7	4:53490917	CTAGCTTTGCTCCCA[-/T]TTTTTTTTTAAAAGG	84708
rs146045438	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53572024	CAAGAAATGAACACA[A/G]CTCCCCAGCACAAAT	84708
rs146046345	snp	C/T	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53616792	AGGAAATGGAGGCAA[C/T]GATGGGTTACTTGAT	84708
rs146048328	snp	C/T	0.0178098	0.0926698	intron-variant	LNX1	GRCh38.p7	4:53491936	GGGATCACAGGCGTG[C/T]GCCCCCACCCCTGGC	84708
rs146095628	snp	C/T	0.000399281	0.0141238	missense	LNX1	GRCh38.p7	4:53496205	TTCCAAGCTGCTCCT[C/T]GGGGCTACTTTTGTT	84708
rs146095724	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53613396	TGTGCAGGATGTGCA[A/G]TTTCATTACATAGTA	84708
rs146131445	snp	C/T	1.64779e-05	0.00287031	intron-variant, missense	LNX1	GRCh38.p7	4:53557905	AGTGCAGGTTGCCCA[C/T]ATTGTCAATGTAGTT	84708
rs146152504	snp	A/C	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53496732	GAAGATAAGGTAGGA[A/C]AAGGCAAAAGAAAAG	84708
rs146168883	snp	C/G	0.0197687	0.0974348	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS2	GRCh38.p7	4:53591034	TAGCCCCCGTTAAAC[C/G]GGCTGAACAGATCTG	84708
rs146170386	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53515159	CTCTCTCTCCAGGAC[G/T]GAGATGGCTTCCTCA	84708
rs146218780	snp	A/C/T	0.0107246	0.0724382	intron-variant	LNX1	GRCh38.p7	4:53634366	CTCCTGCCTCAGTCT[A/C/T]CCGAGTAGCTGGGAC	84708
rs146270849	snp	A/C/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519370	GGGGAGGTACCCTTT[A/C/G]TCTCCTGTTAATAAC	84708
rs146284102	snp	A/C	0.0448719	0.142907	intron-variant	LNX1	GRCh38.p7	4:53468321	ACCACCAGGCCTGCC[A/C]TAAAAGAGCTCCTGG	84708
rs146291146	snp	C/T	0.00557542	0.0525036	intron-variant	LNX1	GRCh38.p7	4:53535708	TGGCTCTATAGCCAG[C/T]GCCTTACATATGCCA	84708
rs146315949	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	LNX1	GRCh38.p7	4:53654266	ATTTATAACAGTCAA[A/T]TTGGCCTTTTCAACC	84708
rs146318552	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53513376	GAGAAATGCCTTGTC[C/T]GAGTTCAGAGGTGGA	84708
rs146334878	snp	A/T	0.00953873	0.0683987	intron-variant	LNX1	GRCh38.p7	4:53650706	AAACCTCTGTCCCCT[A/T]CCGTGTCCCCCCAAG	84708
rs146354804	snp	A/C	0.0178098	0.0926698	intron-variant	LNX1	GRCh38.p7	4:53495650	CAGTTTCAAGTGATT[A/C]TCCTGCCTCAGCCTC	84708
rs146378122	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53613842	AATGGGATTGCTGGG[G/T]TTAATGGTATTTCTG	84708
rs146382079	snp	C/T	0.0225045	0.103662	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53517420	CTTGCACTCCCTGAG[C/T]CCACCCTCAAATAGG	84708
rs146388590	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53612105	TACAGAAAAGCACAT[A/G]CGAAGGGTTGAGAAA	84708
rs146388665	in-del	-/TAAG			intron-variant	LNX1	GRCh38.p7	4:53490527	CTGCTGCTGAGTAAG[-/TAAG]CTGAGGTTAGAGCTC	84708
rs146391491	snp	A/G	1.64779e-05	0.00287031	missense	LNX1	GRCh38.p7	4:53496091	TGATGGCTAACACAC[A/G]GTCATTCTCCTCAAG	84708
rs146393363	snp	G/T	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53540211	ACATGGCAAAACCCT[G/T]TCTCTAAAAAAAAAT	84708
rs146399102	snp	A/G	1.65589e-05	0.00287736	synonymous-codon, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508101	TGTCATTAAGGAGAT[A/G]GTGGCAGCTGCAGAA	84708
rs146403411	snp	C/T	0.00279162	0.0372561	intron-variant	LNX1	GRCh38.p7	4:53491192	AGGATGTGAGTTGCA[C/T]CGATTGACCTGCAGA	84708
rs146421244	in-del	-/A	0.0138799	0.0821421	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53593808	ACTTTATACAAGAAC[-/A]CCTGTGTCAGGTATC	84708
rs146449230	snp	C/T	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53547197	ATTATCTTTGCATGG[C/T]GTTATCAATTCTAAG	84708
rs146449578	snp	A/C	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53591478	AGCTCCTTGGGCCGC[A/C]GGAGTTGTGACCAGC	84708
rs146460282	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53550906	GGAAATAGATACAGA[A/T]AATGGAGGCAAGCAA	84708
rs146461503	snp	C/T	0.021333	0.101051	intron-variant	LNX1	GRCh38.p7	4:53465990	ACTTTAATTAAATAC[C/T]CTTTCAAAAAATTAT	84708
rs146497826	snp	A/G	0.00953873	0.0683987	nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53603790	CCAGGCCCCAACTCC[A/G]ACACTGGAGATTACA	84708
rs146516908	snp	A/C	0.00636936	0.0560724	intron-variant	LNX1	GRCh38.p7	4:53628316	CAAAACAATCCCATC[A/C]AAAAGTAGGCAAATG	84708
rs146562527	snp	C/T	3.29516e-05	0.00405891	synonymous-codon	LNX1	GRCh38.p7	4:53478680	GGTCATGCCGAGAGA[C/T]TCACCGGGGTCTTTT	84708
rs146574115	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53483386	CAATGATACATTTAC[A/G]AATTGTCTTTCTGCC	84708
rs146581062	snp	G/T	0.0267878	0.112589	intron-variant	LNX1	GRCh38.p7	4:53570021	AGGAAAGAACAGGTG[G/T]TGGAGAGGATGTGGA	84708
rs146585876	snp	C/T	0.00914312	0.0669923	intron-variant	LNX1	GRCh38.p7	4:53631613	CACATTACAAGTATC[C/T]GAGAGACTTAAGAAG	84708
rs146585914	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53486390	TCACCCAGCATCCCT[C/T]TCTTTTTTCTACAGG	84708
rs146622662	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53534420	GAGGCAGGAGGGTCT[C/T]GAGCCTAGGAGATCC	84708
rs146626340	snp	A/G	0.00517822	0.0506191	intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53559114	AGCCAAGCCATGATA[A/G]CAAACTCCACTCCAC	84708
rs146640087	snp	A/C/T			intron-variant	LNX1	GRCh38.p7	4:53535551	TTTTATCATTCTATT[A/C/T]TGTTAGTGAATACTT	84708
rs146688536	snp	C/T	0.00318978	0.0398085	intron-variant	LNX1	GRCh38.p7	4:53630438	CCTTCTTGTTTCAGC[C/T]CTCATACTGGATGTA	84708
rs146691018	snp	A/G	0.00636936	0.0560724	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53506404	GACAGTATTTCCTCA[A/G]CTCCACTTATATTGG	84708
rs146700661	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53587810	CGCTCCAGGAAGACC[C/T]GCTGTTTACTCACAT	84708
rs146701117	snp	G/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53510782	AGGCAGCAATGCTCT[G/T]GACCATGTGCCCTGC	84708
rs146739391	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53644797	TCTGGAAGGTCGTTA[C/T]TACCAACCCAGAGAA	84708
rs146756277	snp	G/T	0.0197687	0.0974348	intron-variant	LNX1	GRCh38.p7	4:53465497	CTGTATTAAGTTACA[G/T]TCTTCTCCAGCAGCT	84708
rs146771090	in-del	-/GGTTGTTTTT			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53504462	GGAATGTTGTGGCTG[-/GGTTGTTTTT]TTTTGTTTTTCTATC	84708
rs146807256	snp	G/T	0.00318978	0.0398085	intron-variant	LNX1	GRCh38.p7	4:53648733	GGCCACTGGAGAAAG[G/T]CCACTAAGTCCTATG	84708
rs146823828	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53529896	CTTCTCTATTCCAAG[A/G]CATGTACAGAGAACA	84708
rs146916916	snp	G/T	0.00914312	0.0669923	intron-variant	LNX1	GRCh38.p7	4:53466711	CACCTGGCTCGGAGG[G/T]TCCTATGCCCAAGGA	84708
rs146921627	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53532858	TCCCTCAAGGAACAC[C/T]GCAGGCTGCCCAGGA	84708
rs146921876	snp	A/G/T	0.00438332	0.0466095	intron-variant	LNX1	GRCh38.p7	4:53579587	AAGCCAGTTGGTGCC[A/G/T]CCTGCAACCAAGAGG	84708
rs146963285	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53650286	GCGGGGTGTGGAGGA[C/T]ATACGGTAGCTCCAG	84708
rs146964647	snp	C/T	0.0209421	0.100162	intron-variant, missense	LNX1, LOC101928879	GRCh38.p7	4:53575690	CACCCCCTGGGCTGG[C/T]TAATCAAGGAGGAAG	84708
rs147028908	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53467136	GCTGGGTACTCCTCT[A/G]AGACAAAACTTCAGA	84708
rs147037492	snp	C/T	0.00716266	0.059414	intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53558309	GTACATTTACATCAC[C/T]GGCTGGGAGCAGACA	84708
rs147059292	snp	C/T	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53590200	GCAGATTCTTAGTGG[C/T]GAGGAACGACTGTCT	84708
rs147069224	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53593417	CGCATAAAGCTTCAC[C/G]GAACAGCCTGGAGAT	84708
rs147163757	snp	C/T	0.000153988	0.00877328	missense	LNX1	GRCh38.p7	4:53476763	CTTACCGTGGTAATT[C/T]CAGCCACATGACCCA	84708
rs147166201	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53479558	AATGGAAAAAGAAAA[C/T]CATCTGTGAAAGCTT	84708
rs147176050	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53484857	TCTGAAAAGGGCCCA[A/G]AAAAGAAGTTGGAGT	84708
rs147181005	snp	A/C	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53624332	GGGGCAATTTCCCCC[A/C]TACTGTTCTAGTGGT	84708
rs147182887	snp	C/T	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53549754	AGGCCACATGGAGTT[C/T]TATTATAATCTTTTC	84708
rs147223497	snp	C/T	0.0111196	0.0737302	intron-variant	LNX1	GRCh38.p7	4:53620342	CAAACTCTCAAGCCC[C/T]GACCCAGATGTAGTG	84708
rs147271049	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53503888	CCTGTAATCCTAGCA[C/T]TTTGGGAGGCCGAGG	84708
rs147272442	snp	C/T	0.00676609	0.0577691	intron-variant	LNX1	GRCh38.p7	4:53554267	CCCAGTAAAACCCAG[C/T]GTCTCATTTGCCAGT	84708
rs147282118	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508752	AGCATTGCTATCCTC[C/T]AGTGGCAGCTTGGTG	84708
rs147311226	snp	A/G/T	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53641847	TTATTCATATTGTAG[A/G/T]TATCAACAGTTCATT	84708
rs147324591	in-del	-/TGATTTGCC	0.0349115	0.127424	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508343	GTTGAACTTGGAATT[-/TGATTTGCC]TGCCGCTATATCCTC	84708
rs147331868	snp	G/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53563829	TGGGCCACTGCACCT[G/T]GCCAGGTTAACTTCA	84708
rs147375914	snp	A/G	0.00438332	0.0466095	intron-variant	LNX1	GRCh38.p7	4:53571318	GCCTCCATGCCCCGC[A/G]TAAATTAAGAATCTT	84708
rs147377797	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53523145	AACTAGATTGAAGAA[C/T]AGGACCCTCCAGAGA	84708
rs147391724	snp	A/G	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53586197	TGTGGAAGATGTAAT[A/G]TAAGTCAGACAATCA	84708
rs147435252	snp	A/C	0.0142736	0.0832652	intron-variant	LNX1	GRCh38.p7	4:53583002	GCCCTAGCTGTAACT[A/C]CTAAATCAGGTTACT	84708
rs147480472	snp	C/T	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53545509	TCAGCCTCAATAAAT[C/T]AGAGTTTTCTCATCA	84708
rs147490058	snp	C/T	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53549333	AGTAAATTAAAACCA[C/T]TGTTCTATTTTTCTC	84708
rs147492649	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53462154	GAATGGAAACAGAAA[C/T]GTTTAAAGATTATAA	84708
rs147497361	snp	C/G	0.0023933	0.0345097	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53602266	GACGAAATTAAATAT[C/G]CAGGGACTTGATTAG	84708
rs147530768	snp	C/G/T	0.00636936	0.0560724	intron-variant	LNX1	GRCh38.p7	4:53642706	CCCTTGCTCTACTCA[C/G/T]CAAAATCAGCAAGCC	84708
rs147540626	snp	C/T	0.0023933	0.0345097	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53598301	GCAGTGGCACAATCA[C/T]GGTTTACTGTAGCCT	84708
rs147540641	snp	A/G	0.00438332	0.0466095	intron-variant	LNX1	GRCh38.p7	4:53646972	AAGCTGTAAAAGGCA[A/G]GAAGTGTCCCGGCAG	84708
rs147565558	in-del	-/TGT	0.183568	0.241012	intron-variant	LNX1	GRCh38.p7	4:53464522	AATATGGACAATCAG[-/TGT]TGTTATAAACTCATA	84708
rs147573162	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53610103	AAACCTCCATATTCC[C/T]GATCTAAAGTATTTT	84708
rs147574147	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53537207	GCAGCTAACTTGCAC[A/G]AACATCTGACGCTTC	84708
rs147603381	snp	A/T	0.00636936	0.0560724	intron-variant	LNX1	GRCh38.p7	4:53497407	CTTGGAATGGGCTTT[A/T]CAAAGGCCTTTCTTG	84708
rs147629162	snp	A/C/T	0.00119737	0.0244387	missense	LNX1	GRCh38.p7	4:53496339	ACCTGGCAGGGCTGC[A/C/T]GCAGGAGACGCACAG	84708
rs147636390	snp	C/G	0.00279162	0.0372561	intron-variant	LNX1	GRCh38.p7	4:53543098	ACTCCTGAGCTCAAA[C/G]AATTCTCCTGCCTCA	84708
rs147680423	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53558598	AGTGACAGCTTCCTC[A/G]CTAATTTTGAAATCT	84708
rs147709262	snp	A/G	0.00953873	0.0683987	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519947	AGTCCAAGGCAAACC[A/G]ATGTGCTGGTGCTCA	84708
rs147730137	in-del	-/TAAAT	0.0166325	0.0896639	utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460533	AAAATATTTTAGCTG[-/TAAAT]TAAATTAAAAATGGC	84708
rs147737569	snp	G/T	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53636034	GCAGGTCAGTTAAAA[G/T]CTCTGTGTTGCAGTG	84708
rs147741449	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53561255	TTTTTTTGAGATGGA[A/G]TCTCATTCTGTCACC	84708
rs147751410	snp	C/T	0.00557542	0.0525036	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53516967	AACTGCTGCCCCTGC[C/T]TGCCAGTCACACTCT	84708
rs147781772	snp	C/T	0.0111196	0.0737302	intron-variant	LNX1	GRCh38.p7	4:53620769	AGACATTTCTTTCCT[C/T]CCAGTGCTTAGAGTC	84708
rs147844191	snp	A/G	0.00398564	0.0444627	intron-variant	LNX1	GRCh38.p7	4:53579193	ACAGAGCTGTGATAC[A/G]GTGTTTTGGCAGTTT	84708
rs147847312	snp	A/G/T	0.000812176	0.0201355	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498599	CAGAAGCATTTTTTT[A/G/T]TATCAAGCCCCTTGC	84708
rs147887464	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53592864	CAAGGGGGAGGAGAA[A/G]GAAGAGAAATTGTAG	84708
rs147887505	snp	A/G	0.00478085	0.0486577	intron-variant	LNX1	GRCh38.p7	4:53638739	AGAGAAGCATCATTC[A/G]GGCATGAGTTATAGC	84708
rs147903831	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53636452	GAGACATTCTTGTCC[C/T]TCAGAGTAGAAAAAG	84708
rs147919633	snp	C/T	0.00517822	0.0506191	intron-variant	LNX1	GRCh38.p7	4:53474258	GGAGTGTATATGCTA[C/T]CATTGTGTTTGTGTG	84708
rs147952640	snp	C/G	0.0107246	0.0724382	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53521310	GATATCGAGATGGAG[C/G]TGTGGGGGAAGGTGA	84708
rs147962492	snp	C/T	0.00716266	0.059414	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53523443	AGGCGTGCACCACCA[C/T]GCCTGGCTTATTTTT	84708
rs147992678	snp	A/G	0.0056545	0.0528704	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507412	CGAAGAACACTCAAA[A/G]CTCGATTTATTTTTT	84708
rs147998816	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53602113	GGGACAGAGTGAGAA[A/C]TAGAAACTAGGATCT	84708
rs148000168	snp	A/G	0.000798403	0.0199641	intron-variant, synonymous-codon	LNX1, LOC101928879	GRCh38.p7	4:53576072	ACTCTGCATCCCCCA[A/G]GACCTGGTCGGGGAC	84708
rs148013635	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53472794	ATATAGAGGCCAAGC[A/G]GGGGGAAGGCTGATA	84708
rs148033059	snp	C/G	0.00358779	0.0422022	intron-variant	LNX1	GRCh38.p7	4:53633365	GTCTCTATTCTCTTT[C/G]TCTTCTCCTTTTTAT	84708
rs148044702	snp	A/T	0.00358779	0.0422022	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53514047	ATGCCTTCCCCAGAT[A/T]CCCATCCAGTTTGTT	84708
rs148060948	snp	A/G	0.00676609	0.0577691	intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53559582	CTCAGAGTGCTAGTA[A/G]GAAGGTGAAATGAGG	84708
rs148065023	snp	C/G	0.00517822	0.0506191	intron-variant	LNX1	GRCh38.p7	4:53527767	CAGCAGGGGAAAAGG[C/G]GCTACCAGGGCTGTC	84708
rs148098163	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53584932	AACATGACACACACA[C/T]CCCCAAATTAAAGAC	84708
rs148100134	snp	A/G/T	0.00835141	0.0640778	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508394	ACACATCGGTACTCA[A/G/T]TATACATTTGCCAAC	84708
rs148150086	snp	C/T	0.00478085	0.0486577	upstream-variant-2KB	LNX1	GRCh38.p7	4:53653087	TTATTAAGTGCTTAC[C/T]GTCTACCAGGTTCTG	84708
rs148150543	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53579981	AGGATTCCATATTAT[G/T]AAAAAGAATCCTTCT	84708
rs148182335	in-del	-/ATA	0.00119737	0.0244387	nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53604274	TCATTTATCACAAGC[-/ATA]ATATGTTCTCCTTAA	84708
rs148192011	snp	A/C	0.00318978	0.0398085	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53597653	TGAGTCTCTCCAGGG[A/C]AGATTTCTGTCTAGG	84708
rs148192973	in-del	-/C	0.0185938	0.0946107	intron-variant	LNX1	GRCh38.p7	4:53543959	AACAAACAGAAAAAA[-/C]CAAACACACATTGAC	84708
rs148215116	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53537661	TCAGCACTGCCAGGA[A/G]CCCCACACAGGTGGA	84708
rs148257586	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53554473	TTAAATTGAATTTGA[A/G]TGCTTTCAGGCATTA	84708
rs148259479	snp	C/G	0.0209421	0.100162	intron-variant	LNX1	GRCh38.p7	4:53468076	GAAGGAAAAAATGTT[C/G]AGGGCAGCCAGAGAG	84708
rs148267038	snp	A/G	0.00358779	0.0422022	intron-variant	LNX1	GRCh38.p7	4:53531576	TTTTAGCTTGAAACT[A/G]GTTTTAAGTTCTTCC	84708
rs148273808	snp	A/G	0.0154538	0.0865337	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53593899	AAGGACAAGCTCATC[A/G]GCAAGCGGCAGAGCA	84708
rs148277048	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53484088	GCCATCTGTGAGGAA[A/G]TAGCCATCCCCAGAC	84708
rs148306987	snp	C/T	0.00557542	0.0525036	intron-variant	LNX1	GRCh38.p7	4:53650651	TCTAGCTCTTTTCAC[C/T]GTTCTATACTACCGC	84708
rs148307958	snp	A/G	0.00676609	0.0577691	intron-variant	LNX1	GRCh38.p7	4:53623055	ACTTAGCTTGGGGCT[A/G]GAAGAGATTTCAAAA	84708
rs148308981	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53548767	TAGCAAAGATATGGA[A/G]TCAAACTAAATGCCC	84708
rs148329662	in-del	-/A	0.396551	0.218935	intron-variant, utr-variant-3-prime	LNX1, LOC101928879	GRCh38.p7	4:53576642	TAATAAAAATAAATT[-/A]TAAAAAAAAAAGAAT	84708
rs148359117	snp	C/T	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53616049	CCTGCTCCTCACCAC[C/T]CCCGTCCTTCCAAGA	84708
rs148371553	snp	A/G	0.0023933	0.0345097	intron-variant, nc-transcript-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53501938	GTCTTCTGGAAACAC[A/G]GCTCCAATCCTGCAA	84708
rs148408443	snp	C/T	0.00358779	0.0422022	intron-variant	LNX1	GRCh38.p7	4:53624635	CCCTCACTGCCTACC[C/T]TCCCACCATGCTGAA	84708
rs148431982	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53479211	GGAATCTTAAGCACA[C/G]AGAGTGAACTGCACC	84708
rs148463575	snp	A/C	0.00398564	0.0444627	intron-variant	LNX1	GRCh38.p7	4:53619371	CCCTTCTTTTCCCAG[A/C]CCTGGCAATCACTAA	84708
rs148465178	in-del	-/TAT	0.0138799	0.0821421	intron-variant	LNX1	GRCh38.p7	4:53464051	TTCATTGCTAAGTGG[-/TAT]TATTAGAATAGCAGA	84708
rs148474204	snp	A/G	0.00318978	0.0398085	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53505728	AGAAAAATAATCCCT[A/G]CACTTTGAGGTACAG	84708
rs148527442	snp	A/G	0.0158469	0.0875917	intron-variant	LNX1	GRCh38.p7	4:53496955	ATGGAGTGTATGTGC[A/G]TGTGATACTGTGTGT	84708
rs148555304	snp	A/G	0.0158469	0.0875917	intron-variant	LNX1	GRCh38.p7	4:53635521	CCATTTGGTATTAAT[A/G]TATTGCAATTATTTT	84708
rs148566819	in-del	-/A	0.00755907	0.0610114	intron-variant, downstream-variant-500B	LNX1, LOC101928879	GRCh38.p7	4:53578061	CTTGTCAATCACACC[-/A]AAAAAAAGAAACAAA	84708
rs148576207	snp	A/T	0.0126979	0.078662	intron-variant	LNX1	GRCh38.p7	4:53571913	TGATCCTCCTGCCTC[A/T]GCCTCCCAAAATGCT	84708
rs148586032	snp	A/G	0.00835141	0.0640778	intron-variant	LNX1	GRCh38.p7	4:53529326	GCAGGCAGTGGGGAC[A/G]GCAGCATAGTTGAGG	84708
rs148619585	snp	C/T	0.02016	0.0983543	intron-variant	LNX1	GRCh38.p7	4:53587525	AGGAATAGTTGTATG[C/T]TACTGGGAAGTCCAT	84708
rs148623729	snp	A/G	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53472938	ATAACTGAGTTTGCT[A/G]GTTTCTGAGTTAAAT	84708
rs148640781	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53522498	TTGCTTAGTGCTGGG[A/T]CCTTAGGGTTTTATT	84708
rs148682365	snp	A/C	0.0217236	0.101931	intron-variant	LNX1	GRCh38.p7	4:53546571	TAGCTTGTTACTGGC[A/C]GGGCTGAGTCATTTG	84708
rs148731887	snp	G/T	0.0189856	0.0955633	intron-variant	LNX1	GRCh38.p7	4:53644727	CAGCAGGGCCTCCTT[G/T]CCAGATGGCCAGGCA	84708
rs148767848	snp	A/G	0.0154538	0.0865337	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53595522	ATATGCCATTTCGGC[A/G]ACCACATGATCTTTC	84708
rs148788221	snp	C/T	1.64741e-05	0.00286998	missense	LNX1	GRCh38.p7	4:53476861	TCTTCCTGGGGCTCA[C/T]ACTCTTTGACTTCCA	84708
rs148799061	snp	G/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53485593	TGCAAGACTGGATCT[G/T]TGGCTCTTACCAGCC	84708
rs148822541	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53495005	AGGAGGACGTGGGGC[A/G]GGGAGGGAAATGGAT	84708
rs148840316	snp	G/T	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53543800	CATGCCAAGAAAGAA[G/T]AGAGCAGCTTATGTC	84708
rs148862051	snp	C/T	0.0256215	0.110247	intron-variant	LNX1	GRCh38.p7	4:53615840	TACAGGCATGCAATG[C/T]GTAATAATCTTATCA	84708
rs148873176	snp	A/G	0.0154538	0.0865337	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53596502	GTTTATAATGGTCAC[A/G]AGACCTATATCTTAT	84708
rs148874669	snp	A/T	0.0267878	0.112589	intron-variant	LNX1	GRCh38.p7	4:53570649	TGCACATGTACCCTA[A/T]AACTTAAAGTATAAT	84708
rs148876188	snp	G/T	0.00795532	0.062565	intron-variant	LNX1	GRCh38.p7	4:53488372	TCTCATTGCTCTCTC[G/T]TAGCTCTTTCCCTTT	84708
rs148910237	snp	A/G	0.000153988	0.00877328	missense	LNX1	GRCh38.p7	4:53478729	TCATGACAAGTAATT[A/G]TAGGATGGAGGGGCT	84708
rs148925132	snp	A/T	0.0310518	0.120672	intron-variant	LNX1	GRCh38.p7	4:53638984	GCAATTCCATTACAG[A/T]TATATATCCAAAAGA	84708
rs148926260	snp	A/G	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53564279	AGCTGAGGGGCACCT[A/G]TGTCATCTTTCTCCT	84708
rs148927406	in-del	-/AG	0.108048	0.20579	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53516923	CAGTCAGCTCCTTGC[-/AG]AGACTCCCTGACCAT	84708
rs148933757	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53626884	ATCTGTGCCAACAGT[C/T]TGAAATGGAAATTGA	84708
rs148936202	snp	C/T	0.00835141	0.0640778	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53521514	CTCGGGGTTTGGAAA[C/T]GTGTCATGCAAAGAT	84708
rs148984974	snp	C/T	0.00438332	0.0466095	intron-variant	LNX1	GRCh38.p7	4:53622520	TCACCCCAGGGCTAG[C/T]AATGGACCATTATCT	84708
rs149046185	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53579871	GGCATGTGGCAACGA[C/T]AATTTTACGTGTTCT	84708
rs149051373	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53466460	CCAACTGAGATACTG[A/G]GTTCATCTCACTAGG	84708
rs149079993	snp	A/G	0.00636936	0.0560724	intron-variant	LNX1	GRCh38.p7	4:53637194	AAAACACAACATCAT[A/G]ATTGCAGCATCATGG	84708
rs149084976	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53530993	AACATGGTAAAACCC[C/T]GACTCCACAAAAAAT	84708
rs149101450	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53574674	AAGTGGGCTCTGGAC[A/G]CTTTGCCTGGGTTCA	84708
rs149124102	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53649641	TCATCCTTCCTGCAC[A/C]CCACTCCCTTTACTC	84708
rs149136676	snp	C/T	0.00517822	0.0506191	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53599503	GCCCTTGGGCCTGCT[C/T]TGTCTATGGAGTAGC	84708
rs149136906	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53526768	TTTCTCTTGAACTTT[G/T]GTAACCTCTGGAACT	84708
rs149142380	snp	A/G	0.00795532	0.062565	intron-variant	LNX1	GRCh38.p7	4:53589554	GGCATTGGTCGCTGG[A/G]TGCTAACATATATTA	84708
rs149202349	snp	C/T	0.0225045	0.103662	intron-variant	LNX1	GRCh38.p7	4:53470660	CAGGATACAAATCAA[C/T]GTGCAAAAATCACAA	84708
rs149205463	snp	C/T	0.00478085	0.0486577	intron-variant	LNX1	GRCh38.p7	4:53548418	GTAGTAGTATATGTA[C/T]ATAATTTTATATAGA	84708
rs149239049	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53601968	AACCCTCCTCACCCC[C/T]GCTCACGTGACTGAC	84708
rs149248225	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS2	GRCh38.p7	4:53590961	CAGGTTTAGATCAAA[A/C]TACAGGGAGGAAGAA	84708
rs149250867	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53478460	AAGTCCTGGCCGATC[A/G]CTCCCACATTCTCTC	84708
rs149303829	snp	C/T	0.00676609	0.0577691	intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53559467	GTTAGAGTTCTAGCT[C/T]TGCTGCATACTAGCT	84708
rs149346825	snp	C/T	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53496859	CCCTGGGTCAACTCA[C/T]ACCAGAACTTCCAGT	84708
rs149379569	in-del	-/A	0.00914312	0.0669923	intron-variant	LNX1	GRCh38.p7	4:53625128	TGTGAAACTCTTGGG[-/A]AAAAAACATAAGAGT	84708
rs149389431	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53545256	CCATCTTCAGCATAA[G/T]TTTAACTGGCCAGAG	84708
rs149401022	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53491159	TATTGCGAAGTATAG[C/T]TGGCAAACATTATCT	84708
rs149419250	snp	C/T	0.000399281	0.0141238	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508000	CCCCTAGTTCGGTTG[C/T]TCCGGCCAGAGTCCA	84708
rs149440996	snp	C/T	0.0111196	0.0737302	intron-variant	LNX1	GRCh38.p7	4:53611576	AGTAAGGGACATCCT[C/T]GCTAGTTACTAGAAC	84708
rs149444029	snp	C/T	0.00358581	0.0421906	missense	LNX1	GRCh38.p7	4:53496090	TTGATGGCTAACACA[C/T]GGTCATTCTCCTCAA	84708
rs149449434	snp	A/G	0.00478085	0.0486577	intron-variant	LNX1	GRCh38.p7	4:53641559	ATACCCAGGGGTTCA[A/G]CCTAATGCACATATT	84708
rs149452462	in-del	-/GGGCACAAGACAGGG			intron-variant	LNX1	GRCh38.p7	4:53568581	TTCCCTTTGAAAACG[-/GGGCACAAGACAGGG]GGCACAAGACAGGGG	84708
rs149458092	snp	A/G	0.00993419	0.0697739	intron-variant	LNX1	GRCh38.p7	4:53629233	GATTAGGGGGCTACC[A/G]AAATAGAGGGGTGGC	84708
rs149463897	snp	A/C	0.00159617	0.0282053	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53522252	GTGGCCACCACTCAA[A/C]CAAATCCTACTCTTT	84708
rs149514533	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53593743	ACTAGAAAAAAATGT[A/T]ATCATAAAAATGAAC	84708
rs149515634	snp	A/C	0.00318978	0.0398085	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53518087	GGAAAAATTCAAAAC[A/C]AGCTGGAAAGTCATG	84708
rs149558702	snp	C/T	0.0193772	0.0965046	intron-variant	LNX1	GRCh38.p7	4:53540736	TATTATAAACAGAGC[C/T]ACAGACTGTGTAGAC	84708
rs149601171	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53581970	CATTCATTTTGCATT[G/T]TTTTAAATATTGCAT	84708
rs149609945	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53534048	CTGACAGTCACAGCC[A/T]ACTTTACGAGTGTAT	84708
rs149621132	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53485269	CTTTGGGGAAACTCC[A/G]ATGTTTTGAAGGATC	84708
rs149631003	snp	G/T	0.0001541	0.00877647	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461605	GCACCTGAAATAGAA[G/T]GTAATCAGTGTACAT	84708
rs149651531	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53650531	CTCTGTGGTGTTGGA[C/T]TGGAATTGGAAGTAT	84708
rs149680127	snp	A/T	0.219648	0.248151	intron-variant	LNX1	GRCh38.p7	4:53470152	TCCACCATGATCAAG[A/T]GGGCTTCATCCCTGG	84708
rs149689122	in-del	-/T	0.1652	0.235179	intron-variant	LNX1	GRCh38.p7	4:53648454	ATTGGGTTGTTTTTT[-/T]GTTGTTGTTGAACTG	84708
rs149702386	snp	C/T	0.00438332	0.0466095	intron-variant	LNX1	GRCh38.p7	4:53583564	ACAGAAAAAAAAAAC[C/T]CTTTTAAATGGTCTT	84708
rs149709751	snp	C/T	0.0236746	0.106192	intron-variant	LNX1	GRCh38.p7	4:53608995	GTGAGAATCAGAATA[C/T]CCAACTTCAAACCAT	84708
rs149711636	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53536389	GTCGTTCCCTAAGGA[A/T]CTCTTACAAAAATGG	84708
rs149721934	snp	C/T	0.00914312	0.0669923	intron-variant	LNX1	GRCh38.p7	4:53486915	AAGAGAAGAAAAACA[C/T]AGTCCAGAAGCCTCA	84708
rs149733523	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53465208	TGGCTGCCCAGTTTA[C/T]ATCTTTAAAAAGTTG	84708
rs149752593	snp	A/T	0.0314385	0.121371	intron-variant	LNX1	GRCh38.p7	4:53652075	AGACAGAGAAAGAGA[A/T]AGGGGTGAGAGCTGG	84708
rs149762084	snp	A/C	1.64781e-05	0.00287033	missense	LNX1	GRCh38.p7	4:53478691	GAGATTCACCGGGGT[A/C]TTTTTGGATATTTAC	84708
rs149764909	snp	C/T	0.00279162	0.0372561	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53603186	CCTGGTTGTGCTGGC[C/T]GTGGGGCCATGGAGG	84708
rs149769065	in-del	-/ACAGAAGTAG			intron-variant	LNX1	GRCh38.p7	4:53590506	AGTTTGACTATTGGG[-/ACAGAAGTAG]CTGTCAAGATACAGG	84708
rs149774712	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53564143	CTGCTGTTTTCCAAA[A/C]GTGCATCTCATTATG	84708
rs149775399	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53481531	GCACCTTCTTCTCTC[C/T]TGCTTGGATGGGAGA	84708
rs149789223	in-del	-/TTTT			intron-variant	LNX1	GRCh38.p7	4:53491792	CTGAGGATACGATAC[-/TTTT]TTTTTTTTGTTTGTT	84708
rs149826743	snp	C/T	0.00318978	0.0398085	intron-variant	LNX1	GRCh38.p7	4:53634659	ACCTACTTACTACCT[C/T]TCATGCAGGAAGGGT	84708
rs149827033	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53560574	TTACTGGGTAAGGCA[A/T]CTCAGAAGGCTCTTT	84708
rs149917864	snp	A/G	0.00199481	0.0315187	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53515581	TTCATGTATTTCCCT[A/G]GTAATTTTGATATGA	84708
rs149923767	snp	A/T	0.0256215	0.110247	intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573495	ATCATGACCATAAAC[A/T]CCTAGCTGTTTTTTT	84708
rs149925831	snp	A/G	0.0150606	0.0854603	intron-variant	LNX1	GRCh38.p7	4:53493031	CTGGAGTGCAGTGGT[A/G]CGATCTTGGCTCACT	84708
rs149959711	snp	A/G	0.000131878	0.00811922	missense	LNX1	GRCh38.p7	4:53496289	CATTGTTCCTGCTGC[A/G]GAACTTCTGTTCACG	84708
rs149966434	snp	C/T	0.0225045	0.103662	intron-variant	LNX1	GRCh38.p7	4:53613878	AGGTCTTTGAGCAAT[C/T]GCCACACTGTCTTCC	84708
rs149969546	snp	C/T	0.00874735	0.0655527	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53510326	TCATCTTCTTTGCTG[C/T]TATATGAACATACCT	84708
rs149974830	snp	A/G	0.00478085	0.0486577	intron-variant	LNX1	GRCh38.p7	4:53644193	ATCACTTGAGGCCAG[A/G]AGTTTGAGACCAGCC	84708
rs149975454	snp	A/G	0.0119091	0.0762411	intron-variant	LNX1	GRCh38.p7	4:53569991	ACCAGTTAGAATGGC[A/G]ATCATTGAAAAGTCA	84708
rs149985404	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53525738	GTTCTTCTTGGATCA[A/G]TGCTATGGTAGGCAA	84708
rs150026404	snp	A/G/T	0.00755907	0.0610114	intron-variant	LNX1	GRCh38.p7	4:53638024	GATGGCAGCCACGAT[A/G/T]GTGGCATTTTAACAA	84708
rs150035905	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53595323	TGATTGCTAAATTTA[A/G]ATGGGCTGAGACTGT	84708
rs150040275	snp	A/G	0.00636936	0.0560724	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519761	TTAATCTTCACAACA[A/G]CCTCATGAGATGGGC	84708
rs150074932	snp	A/G	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53645815	TGTCTCAATAAAGAT[A/G]TTTTGAATGAATATC	84708
rs150088904	snp	C/T	0.00279162	0.0372561	intron-variant	LNX1	GRCh38.p7	4:53527796	TCAGCTACTGGACTT[C/T]GTGAGGACAATGACT	84708
rs150154523	snp	A/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53600200	TTTTTATGCTGTCCA[A/G]TAGAGTACTCTGTCC	84708
rs150164447	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53601524	GACCAACACTGTTCG[C/T]GTTCTGGCCACCTGC	84708
rs150177369	snp	A/C	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53477869	CTCTTAAGATACCAT[A/C]CCCCTGTGGCTCCTC	84708
rs150204623	in-del	-/G	0.0310518	0.120672	intron-variant	LNX1	GRCh38.p7	4:53621930	ATAGGCAATCCTGTA[-/G]GTCTCCCCCACTACC	84708
rs150270211	snp	C/T	0.0322114	0.122752	upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53592770	AGGAAGAAGGAAAAA[C/T]GGGAGAGGGAAGAAA	84708
rs150274451	snp	C/T	0.0023933	0.0345097	upstream-variant-2KB	LNX1	GRCh38.p7	4:53653664	GACTTTCAGAGCCAG[C/T]TGCTACAAGTTTCTT	84708
rs150277056	in-del	-/AATC	0.326741	0.23793	utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460624	TCAGTGGGGTATACA[-/AATC]AATCATTTTAGTTGT	84708
rs150279335	snp	A/G	0.0829062	0.185956	intron-variant	LNX1	GRCh38.p7	4:53552722	TAGTCCCAGCTACTC[A/G]GGAGGCTGAGACAGG	84708
rs150286885	snp	A/G	0.00874735	0.0655527	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53605413	TCTTACATGGTAACT[A/G]CCTTGTGTATGCGTG	84708
rs150291086	snp	G/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53499533	GCTGTTCCATGGTTC[G/T]CTGCATATATCTCTG	84708
rs150298229	snp	A/G/T	0.0437457	0.141368	intron-variant	LNX1	GRCh38.p7	4:53484424	AAAAATCAGCCAGTC[A/G/T]TGGTGGCAGGCACCT	84708
rs150358881	snp	A/T			splice-acceptor-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461044	GAATATCACCACATC[A/T]AAAAAAAAAAACAAA	84708
rs150428031	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53561682	CTGGATGCAAAGTTA[A/G]TCCGGAAAATATTCC	84708
rs150438258	snp	C/T	0.00795532	0.062565	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53517919	AGGCTGAATGGCCCT[C/T]GCCCCAGAGGACAGG	84708
rs150443773	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53650399	GACAGTGGTCATGAT[A/G]GCAGTTGATGACATT	84708
rs150444471	snp	A/G	0.00438332	0.0466095	intron-variant, synonymous-codon	LNX1, LOC101928879	GRCh38.p7	4:53576234	TCGCTTCCTGCAGCC[A/G]AGGGTCCTGATGCAG	84708
rs150449377	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime, downstream-variant-500B	LNX1, FIP1L1	GRCh38.p7	4:53459935	ATACATTTTTGATAT[C/T]ACAACTTTTTGATGG	84708
rs150482753	snp	A/G	0.0232847	0.105357	intron-variant	LNX1	GRCh38.p7	4:53631205	CCCACTACCTGGTGA[A/G]AGTGAAGGATCGGGA	84708
rs150490058	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53589105	CCCTGGAGATAGCAC[A/G]ACTGACAGCAAAAAG	84708
rs150494500	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53512431	TTCTTTCTCAGTCCT[A/C]TAGAATGCAACACTA	84708
rs150529654	snp	A/G	0.00318978	0.0398085	intron-variant	LNX1	GRCh38.p7	4:53637715	CACACCATCAATTAC[A/G]TAAACCAAAACACAG	84708
rs150534510	snp	A/G	0.0107246	0.0724382	intron-variant	LNX1	GRCh38.p7	4:53563247	TTTATTTAGATGCAT[A/G]TTTATTGAGTAAAGT	84708
rs150534887	snp	C/T	0.00478085	0.0486577	intron-variant	LNX1	GRCh38.p7	4:53533520	TCTCCTTCCTCAGCC[C/T]CCTGAGTAGCTGGGA	84708
rs150544065	snp	C/T	0.00755907	0.0610114	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519694	GCACATGCACACACA[C/T]ACACTCCTTAACAGG	84708
rs150585187	snp	C/T	0.00318978	0.0398085	intron-variant	LNX1	GRCh38.p7	4:53633721	TGTTTGACATGAGCG[C/T]CCTCATCCATCTTCC	84708
rs150595275	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53590280	ATTTACATGCATTTT[C/G]TATTTCTGGGTGGAT	84708
rs150604437	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53544585	CCAAGGAGGCCAAAA[G/T]GTGGGTACTTCAGGG	84708
rs150627742	snp	A/G	0.00478085	0.0486577	intron-variant	LNX1	GRCh38.p7	4:53648250	TCCAATTTCTCCATG[A/G]CCTTCACAACATTGG	84708
rs150646552	snp	C/T	0.0146672	0.084371	intron-variant	LNX1	GRCh38.p7	4:53585226	GATATCTCACACTGT[C/T]GACTGGAAGAACTCA	84708
rs150667280	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53490344	AGACAGTTCCAAAAA[G/T]CTGCCTCTTTCATAC	84708
rs150682308	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53583566	AGAAAAAAAAAACCC[C/T]TTTAAATGGTCTTTA	84708
rs150689449	snp	C/T	0.00914312	0.0669923	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53603065	TCAAGTCTAAAATTC[C/T]AAAATCAATGCTCAG	84708
rs150689837	snp	A/G	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53529650	GACAGCTCCATGTAC[A/G]TTGTGAGCTCCCAGA	84708
rs150740791	snp	A/G	0.00557542	0.0525036	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53598117	TATTCCTCCATCTGC[A/G]GGGCTCAGCTCAGAT	84708
rs150750192	snp	C/T	0.00676609	0.0577691	intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53560179	ATAGATCAGAACTCT[C/T]AAGTAGCATGATGTA	84708
rs150754187	snp	C/T	0.00279162	0.0372561	intron-variant	LNX1	GRCh38.p7	4:53473461	ATACATCATGGAATA[C/T]GATGCAGTCATAAAG	84708
rs150762733	snp	A/C	0.00636936	0.0560724	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53509142	TAGGTTTTGGTCAGG[A/C]AATGGTGATTTAACT	84708
rs150802075	snp	C/T	0.0130921	0.0798413	intron-variant	LNX1	GRCh38.p7	4:53628835	TTACAATGACTTGGA[C/T]GAAGCAGGAGGCCAT	84708
rs150804961	in-del	-/ATTTTT			intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53462506	AATCAGATATGGCTA[-/ATTTTT]TTTTGTTTATATACC	84708
rs150805897	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53554882	ATCCTGCCTTGCCCC[C/T]GCAGGCATTTGACTT	84708
rs150813974	snp	C/T	0.0103295	0.0711199	intron-variant	LNX1	GRCh38.p7	4:53581628	CATGTGCAGGGGAAC[C/T]GCCCTTTATAAAACC	84708
rs150836388	snp	A/G	0.00716266	0.059414	intron-variant	LNX1	GRCh38.p7	4:53607887	CTCCCTATTCAAAAA[A/G]TGGTGCTGGGATAAC	84708
rs150857715	snp	C/T	0.00438332	0.0466095	intron-variant	LNX1	GRCh38.p7	4:53623698	TTTTGTTAAAACCAC[C/T]GAGAATTTATAACTA	84708
rs150920680	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53505952	TATAGGACTGTAATA[A/G]GCTGAGAGCTGTTAG	84708
rs150943057	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53583479	CAATGATCTCGAAGA[G/T]GGACTAAGCCACTCA	84708
rs150959646	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53625604	GAATTTGACACCAAA[C/T]TGGGCAACATAGTGA	84708
rs150971831	snp	A/G	0.00835141	0.0640778	intron-variant	LNX1	GRCh38.p7	4:53578546	GTGGAGTCTGTCATT[A/G]ACCAACATGTCGTTA	84708
rs151000270	snp	C/T	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53645332	TGGAGTTTGGCAGAG[C/T]CCTCTTGTGCAGAGG	84708
rs151060746	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53536299	CAAAGCCACCTACCT[C/T]GCAGTGCGAATGAAC	84708
rs151067002	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53521628	CCTCTTCCCTCCCAA[C/T]ATATTTAAAAGAAAC	84708
rs151101975	snp	A/C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53551825	TGGCCTCTCACCCTG[A/C/T]CTTATGACCCTTGGT	84708
rs151118366	snp	A/G	0.00358779	0.0422022	upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53592062	AGCAGTTTCAAAGTG[A/G]TTTTCAAACACTTTT	84708
rs151124685	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53480853	AAAAGGGCATTCCCT[A/G]CTTTCTGTTGCAAGA	84708
rs151131226	snp	A/G	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53546830	GCTGGGGAGGGAGTC[A/G]GGGGCAGAGTCAAGA	84708
rs151140045	snp	A/G	0.433963	0.169285	intron-variant	LNX1	GRCh38.p7	4:53471072	AGCTGGAGGCATCGC[A/G]CTACCTGACTTCAAA	84708
rs151152267	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53650176	AGCTTTGTCCCCCAT[A/C]AAAGACAGTGACAAC	84708
rs151183105	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53541867	ATAGCTTTGTAATAA[A/G]TGAAATTTGGAGAAT	84708
rs151214373	snp	C/G	0.00279162	0.0372561	nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53604563	TTATGGGTTGTGGTA[C/G]TGGCATTCAGGCCAG	84708
rs151269186	snp	A/C	0.00199481	0.0315187	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53599803	CCGAGAAAACCTATA[A/C]CTCTTATAGCTTTAG	84708
rs151278706	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53561468	CCTGATCTCATGATC[C/T]GCCCACGTCATCCTC	84708
rs151279438	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53475635	CAGTGATGCTAATAT[A/T]TAGCATTATTCACAC	84708
rs151287413	snp	A/G	0.0115144	0.0749975	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53511333	AAAGATGGAAGAAGC[A/G]GGGAAGAGCTGATTA	84708
rs151307827	in-del	-/TCTGACACAC	0.0991586	0.199366	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519656	GTGTCTGTCAAGGTA[-/TCTGACACAC]ATCTGACACACACAC	84708
rs151307935	snp	G/T	6.59011e-05	0.00573988	synonymous-codon	LNX1	GRCh38.p7	4:53476902	TACTATCGAGGATGA[G/T]GTTCTTTTCAATAAT	84708
rs151329306	snp	C/G	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53631020	AACAGGGGAAATGAG[C/G]CAGAACCTTGCAGTA	84708
rs180672304	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	LNX1, LOC101928879	GRCh38.p7	4:53577970	CAGGCACTGTGCTAG[A/G]GGCCTTATATTATAG	84708
rs180675514	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53624868	TAGAATGTATTTATT[G/T]AAGATTCCAGAATTT	84708
rs180678186	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53605772	CCTTTTTAACAGCTG[A/G]ATAATATTCCATTGT	84708
rs180683250	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53560348	ATGAAATTAATTAAT[C/T]AATGTGACTGCAATA	84708
rs180684543	snp	A/C	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53585006	TCTTCCAATTGTCTT[A/C]CTGGGTAGTCCAGAT	84708
rs180705409	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53542388	AGTGTCTTGGGATTT[C/T]ATATTCACTGTTAGT	84708
rs180707320	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53617673	CTATGTGTGCACTGT[A/G]AATGTCTCTCTTGTT	84708
rs180715149	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53637503	TGCTTTGCACTACAC[C/T]TGTCATTTCACATGT	84708
rs180726845	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53596617	GGCTGTTGCTATTTC[A/G]AAGGTTGCCATGTCT	84708
rs180799944	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53483115	CTGGCAGGAGGTAAC[C/T]GATTCATGGGGGTGG	84708
rs180801789	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53533651	GTGATCCGCCCGCCT[C/T]GGCCTCCCAAAGTGC	84708
rs180806017	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53504160	AAAAGAAAATCTGCT[G/T]AGTGGAGCCACCTTC	84708
rs180815510	snp	A/G/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53524985	AGGGAGTCTTAGAGC[A/G/T]TAAAGATGGGGATTT	84708
rs180818657	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53569959	CAAATCAAAACCACA[A/G]TGAGATACTATCTCA	84708
rs180825101	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53551037	TGCAGTTTGTCAGAG[A/G]TGTATGTCGCAGGTT	84708
rs180835567	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53467351	TCAGTACGTCACCAT[C/T]ATCAAAGACCAAAGG	84708
rs180838867	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53487045	TTTGTGTTCAGCCTG[C/G]AACTGACTCTTTCTC	84708
rs180848626	snp	A/C	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53493260	ATGTGAGCCACCACA[A/C]CCAGCCAGAAAATGC	84708
rs180854153	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507899	TCCCCTTAAAAAACA[G/T]TTACAGAACTTTCCA	84708
rs180861302	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53528318	CTATTAAGTAGAAAA[C/T]TCCAGAAACAATTCA	84708
rs180870719	snp	A/T	0.00478085	0.0486577	intron-variant	LNX1	GRCh38.p7	4:53471559	GTGAACAGGCAACCT[A/T]CAGAATGGGAGAACA	84708
rs180880974	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53478300	TAATAGAGGTAACTT[C/G]CTCATAACTGTAGCA	84708
rs180884189	snp	G/T	0.00914312	0.0669923	intron-variant	LNX1	GRCh38.p7	4:53468820	ATGCACCCAATACAG[G/T]AGCACTCAGATTCAT	84708
rs180890270	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53511676	TTTTGTCTCTTTTGG[C/G]GTTGGAGGGGGGATA	84708
rs180902343	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53464682	GTTGACACTGCTACT[C/T]GCAGAGGATAAGGGA	84708
rs180905126	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53581316	AGGTATATCAAAACT[C/T]AAAACATCAATTTAA	84708
rs180910917	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53546082	AAAGTACTGAGATTA[C/T]AGGCATGAGCCACTG	84708
rs180942775	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53591880	GACAGTAATTTAGCA[A/G]ACACAAAAAGGAAGA	84708
rs180948865	snp	C/T	0.0154538	0.0865337	intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53575178	GTAGAGACAGGGTTT[C/T]GCCATGTTGGCCAGG	84708
rs180951113	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53620197	TGTCTATTTATCTAT[C/G]TACCTATCTATCTAT	84708
rs180955966	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53520841	GTGGTGAGTGCCTGT[A/T]ATCCCAGCTACTTGG	84708
rs180962102	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53554899	CAGGCATTTGACTTT[A/G]AGAAACCTGGGCCAC	84708
rs180965599	snp	A/G	0.0387552	0.1337	intron-variant	LNX1	GRCh38.p7	4:53563163	GTGAGCTGAGATCGT[A/G]CCAGCCTGGGCGACA	84708
rs180981063	snp	A/C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53499612	AATCATTTTTAATGG[A/C/G]ATGAATTGCAGTTTT	84708
rs180990482	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53600678	GACACCCCTTTTTAA[C/T]TTGGACATGAACCTG	84708
rs180996728	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53539358	GATGTCCTTTAGTTT[C/G]TCTTTATTGTATTAG	84708
rs181104944	snp	C/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53645722	TGGCCTCTCACATGA[C/G]CACCTTCCCTGAGTT	84708
rs181127292	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53625599	CCCAGGAATTTGACA[C/T]CAAACTGGGCAACAT	84708
rs181129073	snp	A/G	0.0236746	0.106192	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53462021	ATAATCTCAATGAAA[A/G]CAGTTTAAGCCTAAT	84708
rs181143207	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53638314	GTCAATTCTAGTTAG[A/C]AAGACTGTACAATAT	84708
rs181149797	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53497745	ACTGCGGCCTGCCCC[A/G]AGGGCCCTGTCTTAT	84708
rs181278340	snp	C/G	0.00874735	0.0655527	intron-variant	LNX1	GRCh38.p7	4:53528955	TACCCATAAAAAAAA[C/G]CCATCACAGAGGAAA	84708
rs181303300	snp	C/T	0.00478085	0.0486577	intron-variant	LNX1	GRCh38.p7	4:53563476	AGGGGGGCCTACTGG[C/T]CCATCACAGACCCAA	84708
rs181308093	snp	A/C/T			intron-variant	LNX1	GRCh38.p7	4:53547277	AAATATATTCTAACT[A/C/T]CCTCCATTACTCATG	84708
rs181317896	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53620656	TTCACCATAATGCAA[C/T]ACATCAGTGTAGCAG	84708
rs181322337	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53601556	CATAAACTCGCAGCA[A/G]CTGTGACAACTGCGT	84708
rs181331358	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53581997	GCATTCACATTAGGA[C/T]TACTGAATTTTTCTG	84708
rs181354395	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53641598	TGCATCTGATCAATT[G/T]TGGCATACATATATG	84708
rs181402324	snp	A/G	0.00755907	0.0610114	intron-variant	LNX1	GRCh38.p7	4:53468960	AACAAGGATATCCAG[A/G]AATTGAACTCAGCTC	84708
rs181415944	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53537575	AGTATTTTCTCACTC[C/T]TTCCATCTCTCCATT	84708
rs181422075	snp	A/C	0.0023933	0.0345097	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508465	TGCATTCTCTTAAAG[A/C]AATCTCTACATTGGC	84708
rs181428278	snp	C/T	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53621827	GAGTTGGATTCTAAG[C/T]CTGGTGCCAGCCAGT	84708
rs181429587	snp	C/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53641854	TATTGTAGGTATCAA[C/G]AGTTCATTCCTTTTT	84708
rs181438021	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS2	GRCh38.p7	4:53590985	GGAAGAAAAGGAAAA[A/G]TAAGAACTCTGAATC	84708
rs181447571	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53574910	GTTGGCCCAGAAACT[A/G]AAAGCTAGAGCTCCT	84708
rs181457328	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53554544	CTTTGTGTTATGCCC[A/G]AATGATACATGTTTT	84708
rs181500051	snp	A/G	0.00398564	0.0444627	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53602211	ATCTGTGACCTTGAC[A/G]TCACCATCTATTCTA	84708
rs181500558	snp	G/T	0.00438332	0.0466095	intron-variant	LNX1	GRCh38.p7	4:53553897	CCTGATAGCAATAAC[G/T]TAAGCATACCCTGAG	84708
rs181508247	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53631221	AGTGAAGGATCGGGA[A/G]TGGGGTGGGATAATG	84708
rs181509927	snp	C/T	0.00318978	0.0398085	intron-variant	LNX1	GRCh38.p7	4:53563916	TCAGGCATATGGTGA[C/T]TAATACATACAACAT	84708
rs181528662	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519805	CCAGTTTGCAAATGC[A/G]GGAACTTAATACAAA	84708
rs181528824	snp	C/T	0.00676609	0.0577691	intron-variant	LNX1	GRCh38.p7	4:53489294	ATTAGGGCAGCAATA[C/T]GGTTTATTTTTCCCA	84708
rs181555457	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498899	ATGGACCTTTCCAAC[C/T]ACTCTTCTTGCCAAA	84708
rs181558420	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53520493	CATCTTTGGGGTCAC[C/T]GAGTTCATTTCCTCC	84708
rs181575727	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53538985	GTCCAGGAGATCTGA[C/T]GGGTTGAAGGGGATC	84708
rs181589555	snp	G/T	0.00279162	0.0372561	intron-variant, downstream-variant-500B	LNX1, FIP1L1	GRCh38.p7	4:53462906	CTGTGGTGTGTCACA[G/T]AACACACTTTACATA	84708
rs181592497	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53478071	CAAAGTAGCCCAGAA[C/T]ACATGAGCTTAAAGT	84708
rs181600291	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53503452	ACATCATTACTCTTG[C/T]GTCTCCATCGAAGTA	84708
rs181607310	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53472669	ATGATTTATTCAACA[A/G]CAACAACAACAACAA	84708
rs181631926	snp	C/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53650276	AGGCACCTGTGCGGG[C/G]TGTGGAGGACATACG	84708
rs181638222	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53582545	GCCCTACTGTATTCA[C/T]GTTTGCTTTGAATTT	84708
rs181639712	snp	G/T	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53611652	TTTTTACCACTAAAA[G/T]TGCAAAACTGCAATT	84708
rs181770761	snp	A/G	0.00795532	0.062565	intron-variant	LNX1	GRCh38.p7	4:53551307	TGTCAGGCAACCATC[A/G]GGTGATGGTCAGGCA	84708
rs181797694	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53513464	TGATCCCTAGACTCA[C/T]ATCAAACTGCCCATT	84708
rs181811886	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53585463	GGTCCCTGCAAAAGA[C/T]ATATCCATGTCTTAA	84708
rs181842574	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53632033	AAAGCTCCTGGGTCC[A/G]CTGGTTCTTCTAATC	84708
rs181847536	snp	A/C/G	0.00358779	0.0422022	intron-variant	LNX1	GRCh38.p7	4:53650597	GAAATAAATAGATAC[A/C/G]TAAATAGAGGAGGAA	84708
rs181856865	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53612557	TTAAGAATAAATTAA[C/T]GCTTGTAATCCCAGC	84708
rs181935329	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53493538	TTGGTCCTCTTCCAC[A/G]AAGAGGGATAAGCTA	84708
rs181970356	snp	A/C	0.0178098	0.0926698	intron-variant	LNX1	GRCh38.p7	4:53466929	GGGGCAGGGCACAGA[A/C]AAACAAAAGGCAGCA	84708
rs182003167	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53515175	GAGATGGCTTCCTCA[C/T]ATTAGTGCCAGAGAA	84708
rs182006075	snp	A/C	0.00438332	0.0466095	intron-variant	LNX1	GRCh38.p7	4:53466372	AAAGAAACCTGAAGA[A/C]AGCCGAATAGGAACA	84708
rs182009279	snp	C/T	0.00279162	0.0372561	intron-variant	LNX1	GRCh38.p7	4:53534954	AACAGAAAGAAATGA[C/T]TGCTCATGGGTACAA	84708
rs182020345	snp	A/C/G	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53551409	CACCTGAAACTGGTG[A/C/G]TCAGCTTCCTAGTAA	84708
rs182026704	snp	A/G			intron-variant, utr-variant-3-prime	LNX1, LOC101928879	GRCh38.p7	4:53577486	TTTTCAAACTGTGCT[A/G]TGGAAGGCATCAGAT	84708
rs182036763	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53493973	GCTCGCAATATTTCA[C/T]ATGATCTGTCTCTTG	84708
rs182042689	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53636259	ATGCATGCTTGCCTC[A/G]GTCGAGCAAAAACAA	84708
rs182056237	snp	G/T	0.0111196	0.0737302	intron-variant	LNX1	GRCh38.p7	4:53617411	GAAAAGAAAATTTAC[G/T]TTGGGATTTAAGATG	84708
rs182056266	snp	A/G	0.0267878	0.112589	intron-variant	LNX1	GRCh38.p7	4:53570830	CAGGAGATCGAGACC[A/G]TCCTGGCTAACACAG	84708
rs182056806	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53606117	CTGAACCGAAGGAAA[C/T]TGGGAAAAACCATAC	84708
rs182061201	snp	A/T	0.00119737	0.0244387	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53596067	CCGTAATTACTTTTT[A/T]AAATGGGCTCAGCTC	84708
rs182064589	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53534545	TATTCAGAAGGCTGA[C/G]GTGGGAGGATCACTT	84708
rs182100290	snp	C/G	0.00358779	0.0422022	intron-variant	LNX1	GRCh38.p7	4:53526967	TAAAGCAATAGAAAT[C/G]AAACACCTAAATGAA	84708
rs182111540	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53587352	CCCTATTCTTTGGGG[A/C]TAGTTAATGATTAAA	84708
rs182116931	snp	C/G	0.00398564	0.0444627	intron-variant	LNX1	GRCh38.p7	4:53544244	CTGTTGCCCAGGCTG[C/G]AGTGCAGTGGTGCCA	84708
rs182120583	snp	A/G	0.00716266	0.059414	intron-variant	LNX1	GRCh38.p7	4:53468303	ATGCTGAGAGATTTT[A/G]TCACCACCAGGCCTG	84708
rs182120655	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53571385	CCAAGGTAATCACAT[A/G]AGTTCTTATAGGAGG	84708
rs182127484	snp	A/T	0.00438332	0.0466095	intron-variant	LNX1	GRCh38.p7	4:53485301	CAGCAGAGTGTCCAT[A/T]GGCTTGCAAATTGTA	84708
rs182132127	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53552045	AAAGTATAATTTTCT[A/C]TCCAGATTCTATAAT	84708
rs182137156	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53627297	ACGGCCTTTGAAGGT[A/G]CAGGGTGGTCCTCAG	84708
rs182142053	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53646892	CCAATTTAACATGAG[C/T]AAATAAACCACTCCC	84708
rs182152992	snp	C/T	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53608643	ATATAAATTTTTCTA[C/T]CACAAAGACATGCAC	84708
rs182249862	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53503812	CTAGATGGCATCTTC[C/T]CCCAATATAAGGCTG	84708
rs182261017	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53482372	CACTTTAGAAATATG[G/T]GGATGACTTCATACA	84708
rs182272857	snp	A/G	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53541964	ATGCATAAATCAGCT[A/G]CTCCAGATGACACAT	84708
rs182301408	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53640701	AGACTGTGTTGTTAT[A/G]GAAATACTGTGCCTA	84708
rs182313928	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53646402	ACTCTGCTTTATTCA[C/T]ATCCTCTAACCCTGC	84708
rs182334146	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53607370	ATTCACGATGGTCAC[A/G]AAAAGATAAAATACC	84708
rs182342017	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53509688	ACATGACTACAAGCA[A/G]TTCTCATGAGATTGT	84708
rs182349278	snp	C/T	0.00318978	0.0398085	intron-variant	LNX1	GRCh38.p7	4:53529966	TAGAAAAAATGTAGG[C/T]GAATACTTTTCAGAC	84708
rs182362342	snp	C/G	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53548135	TGAAAAAAAAAAAAA[C/G]TCGGGGGAAATATGA	84708
rs182367208	snp	C/T	0.0189856	0.0955633	intron-variant	LNX1	GRCh38.p7	4:53470333	TAGGTATTGATGGGA[C/T]GTATCTCAAAATAAT	84708
rs182380785	snp	A/G	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53491396	TCTCATTGATTGGCC[A/G]GCTAATGCCACCTGC	84708
rs182381442	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53494461	GTCTCCTTAGGATGA[C/T]CCTTGCTGACTTGTA	84708
rs182400074	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53535866	TAACTGTATGTCTAC[A/T]TTTGATATGACCCCT	84708
rs182409161	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53599111	ACATTTGAGTGGCAT[A/G]TGAACCAGGGCAATT	84708
rs182444855	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53561733	ATGTCTTGGGCCAAT[C/T]ACATCACGTTTTCAT	84708
rs182449635	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53639380	AAACTATTGGGTGCT[A/G]TGCTCAGTACCTGGG	84708
rs182457938	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53598415	TTTTTGTATTTTTTG[C/T]AGAGATGGGGTCTTG	84708
rs182463021	snp	A/G	0.00517822	0.0506191	intron-variant	LNX1	GRCh38.p7	4:53578298	GGTGCATTGTTAGGC[A/G]ATTTGGTCCTTGGGT	84708
rs182531872	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53559985	CTAATAACTATTAGC[A/G]ATAGTGAATGAGCCT	84708
rs182540460	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53523640	TGAAATCAGATAGTA[A/G]CCTATTAGTAGGAGA	84708
rs182560875	snp	G/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53586688	AAGTTCTTTCAGATG[G/T]ATAGGTGAAGAAGGG	84708
rs182600364	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53626217	AGAAAATATGTTCGT[C/T]TTCAAGGACTGAGCA	84708
rs182623370	snp	C/T	0.000214315	0.0103495	missense	LNX1	GRCh38.p7	4:53478592	TTCCATCTCTGCTTA[C/T]GACTCCTCCGGGCTC	84708
rs182635356	snp	C/T	0.0023933	0.0345097	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53521068	TATGGATCAACGGTG[C/T]TTTCTATTTCAGGAC	84708
rs182643324	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53515972	ATTCGCACAAAAGGC[C/T]GAGTGTGGTGGCTCA	84708
rs182653510	snp	A/C	0	0	intron-variant	LNX1	GRCh38.p7	4:53465114	TATTGGCCATTGAAA[A/C]ACATCTTGCATTTTT	84708
rs182672641	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53579141	TTTACTGAATGTATC[A/G]GCCATCAGCATCTCT	84708
rs182689654	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53643730	GCCTGGTAACCTTGG[A/G]CAGCTTGCTAAAGCT	84708
rs182693587	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53622327	GACTTTTCAAAGTGC[A/G]TGGATTAGAAATACT	84708
rs182695086	snp	C/T	0.00398564	0.0444627	nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53603738	TGGTGCTAAATCATT[C/T]ATGAGAAATCTGCCC	84708
rs182718421	snp	C/T	0.00279162	0.0372561	intron-variant	LNX1	GRCh38.p7	4:53540202	GTCTAGACAACATGG[C/T]AAAACCCTGTCTCTA	84708
rs182729586	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53619366	TCATTCCCTTCTTTT[C/T]CCAGCCCTGGCAATC	84708
rs182734919	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LOC101928879	GRCh38.p7	4:53575419	AGAAAGTCAATAAAT[A/G]GTTTTCAAGCGCCAA	84708
rs182740468	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53556104	TAAGGATCTCAAGAT[A/G]AGATTACCATGGAGT	84708
rs182746263	snp	C/T	0.00119737	0.0244387	intron-variant, nc-transcript-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53501935	TCTGTCTTCTGGAAA[C/T]ACGGCTCCAATCCTG	84708
rs182752048	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53521694	TTGTGTTATGCAAAC[A/G]AAGGGGGAAAGGAGG	84708
rs182762807	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53613762	TGAATAGCACTGCAC[C/T]GAATATATGGGTGTA	84708
rs182766737	snp	C/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53593729	TATATTTCTAAACTA[C/G]TAGAAAAAAATGTAA	84708
rs182829151	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53583726	GAAAAGAGTCCCAAG[A/T]GGCTAGACAATTAGA	84708
rs182841450	snp	C/T	0.0287284	0.116357	intron-variant	LNX1	GRCh38.p7	4:53564956	GGGCTTAAAAAATGG[C/T]GCACCACGAGATTAT	84708
rs182851109	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53548787	ACTAAATGCCCATCA[A/G]TGACAGTCTGGGTAA	84708
rs182900034	snp	C/T	0.00438332	0.0466095	intron-variant	LNX1	GRCh38.p7	4:53552689	CAAAAATTAGCCAGA[C/T]GTAGTGGCAGGTGCC	84708
rs182909003	snp	A/G	0.00517822	0.0506191	intron-variant	LNX1	GRCh38.p7	4:53627633	AATTTTTAAATAAAT[A/G]CACAGAGGTGAGTAA	84708
rs182928238	snp	G/T	0.00914312	0.0669923	intron-variant	LNX1	GRCh38.p7	4:53526028	TTATTGACATTCAAT[G/T]TTTTAAAATGCAAGC	84708
rs182934373	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53587624	TACAGACGGCATTTC[A/G]AGTAGTCAAGATCGT	84708
rs182935009	snp	A/C	0.00636936	0.0560724	intron-variant	LNX1	GRCh38.p7	4:53542634	GTTAGACATGGGTAC[A/C]TCTGCAATTAGAGAA	84708
rs182936375	snp	C/T	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53495155	TAGGAAAAACAGTAA[C/T]GAGACATGGGATCTC	84708
rs182954017	snp	C/T	0.00398564	0.0444627	intron-variant	LNX1	GRCh38.p7	4:53560855	ACAATTTTCCATTAC[C/T]TGCCATCTGATGTAA	84708
rs182964760	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53504520	GCAATAAGGCTGTTT[C/T]GCTTTGTAAATCATG	84708
rs182966597	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53474891	CATGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA	84708
rs182968190	snp	A/G	0.00159617	0.0282053	intron-variant, downstream-variant-500B, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460017	TTCATATCCAAATTA[A/G]TAAAACCTATAAGGC	84708
rs183002512	snp	C/G	0.0448719	0.142907	intron-variant	LNX1	GRCh38.p7	4:53469787	CCTCCCAAGACTAAA[C/G]CAGGAAGAAGCTGAA	84708
rs183018125	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53651438	AGGAATGGAAGTAAA[C/T]AGGAATACATGACAA	84708
rs183121468	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53470641	AGCAACTTCAGCAAA[G/T]TCTCAGGATACAAAT	84708
rs183166359	snp	C/T	0.00398564	0.0444627	intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53575341	TTCCTTTAACATAGA[C/T]AGGAGTCAACAATAA	84708
rs183176340	snp	A/T	0.00398564	0.0444627	intron-variant	LNX1	GRCh38.p7	4:53615633	AATTGTGAACAATAA[A/T]AAAGGTTGTTGTTTT	84708
rs183178854	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53594406	TCTGAAAATTTAATC[C/T]GAGTGGCCATAAGAA	84708
rs183181430	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53572280	TCCTCCTTTAACCAC[A/G]TCTATTTCTGGGGAA	84708
rs183196922	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	LNX1	GRCh38.p7	4:53654094	TTTGTTCTTAACAGA[C/G]ACTGAAGACTTATTT	84708
rs183205238	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53634392	GGGACTACAGGTGCA[C/T]GCTGCCAGACCTGGC	84708
rs183205683	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53539837	AGGGACAATGGTTTC[A/T]TGTAATCTGCTGAGG	84708
rs183210363	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53510366	AGTGGCATCTTAGAT[C/T]AGATGAAATGTGGTT	84708
rs183216021	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53609038	CAATAACCAAAACAG[A/C]GTGGTACTGGTACAA	84708
rs183219789	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53613108	TATTAATATGGGCTT[A/T]CTGGGTAAGTGGGTG	84708
rs183240578	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53647860	AAGTGGAATTATATC[A/G]TATTTGTCCTTCTGA	84708
rs183255378	snp	C/T	0.00318978	0.0398085	intron-variant	LNX1	GRCh38.p7	4:53529325	AGCAGGCAGTGGGGA[C/T]GGCAGCATAGTTGAG	84708
rs183264400	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53638773	GTTGGCCATGAGCTC[A/C]AAATTGGTGTATTAA	84708
rs183264953	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53588879	CCTGGGCACACAACT[A/G]CTCATATGCAATGAC	84708
rs183305193	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53564364	CCCTTCTGGCTTCAC[C/T]CTCAGATCCACACAC	84708
rs183322529	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53633539	GGGAAGCTGCCATGA[A/G]TTTATCAGTTTTTGC	84708
rs183401785	snp	C/G	0.00478085	0.0486577	intron-variant	LNX1	GRCh38.p7	4:53489981	TACAGTACCACAAAA[C/G]TTCTACCCTTTTTTG	84708
rs183405900	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53465293	CAAACATTTTTGACA[A/G]AACTTCTCTTTACTT	84708
rs183430029	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53555855	GTTATTCAGCAAAAA[C/T]GTTGCCTTTGATTTA	84708
rs183439921	snp	C/T	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53618834	TTCACATATTTATGT[C/T]CCTTTTAAAAAAAAT	84708
rs183441243	snp	A/G	0.00358779	0.0422022	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53598597	AATGTGACTTTCCAC[A/G]TACTCTCAGGACTTA	84708
rs183442035	snp	A/C	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53491622	AAAGCAGATTTGGTG[A/C]TTCTTTGGTAAATGG	84708
rs183449392	snp	G/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53632859	TTTCAGGAATCATTT[G/T]TTTCTCCAGGTCTTC	84708
rs183458491	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53531519	GAAATAGACAGTAGT[A/T]GGGACAATATTTAGT	84708
rs183463556	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53592743	TTTGGGGTTTGGTTT[G/T]GGGGAGGGTGGAGGA	84708
rs183471956	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53547492	GACTGCAGAGCATGT[A/G]CCTTGAATCACTAGG	84708
rs183488823	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53479501	ATGAACCAGTGTCCA[A/T]GACCATTTCCTTTCT	84708
rs183501487	snp	A/G	0.00279162	0.0372561	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53516375	GGATGCAAAGAAAAC[A/G]ACAATGTATGCACTT	84708
rs183517504	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53610791	AAAGAGAGATAAATA[A/G]AGGCAAAAGCTTAAA	84708
rs183523606	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53563240	AAACAATTTTATTTA[C/G]ATGCATATTTATTGA	84708
rs183526161	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53473859	AGTTGAAAAGGATCC[A/G]AGAACACTAAATATA	84708
rs183527324	snp	G/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53483694	TTGGTGGTTCCTCTC[G/T]TCATCCCATCCCTTG	84708
rs183529775	snp	C/G	0.00517822	0.0506191	intron-variant	LNX1	GRCh38.p7	4:53589667	GAGAAGTAACTTGCT[C/G]AAGGATATAAATGAA	84708
rs183534100	snp	G/T	0.000498806	0.0157846	missense, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573997	GGCAGACTCTGGCTG[G/T]TTCATGATGGATTGG	84708
rs183562747	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53652146	TGAGATTCTACCTGG[C/T]GGAGGAACCGGGCCA	84708
rs183638390	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53509190	GGAGGGTAGCTACAG[C/G]TAACCACTCCAGTTT	84708
rs183699101	snp	A/G	0.00517822	0.0506191	intron-variant	LNX1	GRCh38.p7	4:53467635	AATAGCCAATGCAGA[A/G]AAGTCCTTAAAGGAC	84708
rs183726813	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53629845	AAATATTGCAGGTAC[A/G]CCTTGGTTTGATTTT	84708
rs183731214	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53649064	CAAAATATATCAAAA[A/G]ATAAGCAACAGTAAG	84708
rs183746511	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53536372	CGCCACACACAGTCA[A/C]AGTCGTTCCCTAAGG	84708
rs183778568	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53556819	TTACAAAGGAGGCAC[A/G]GGCTACCACTACATA	84708
rs183781591	snp	C/T	0.00557542	0.0525036	intron-variant	LNX1	GRCh38.p7	4:53582608	CTCCCTTCAGCCAAC[C/T]TCTTGTTTTACAGCA	84708
rs183806864	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53622126	CTCTTATTTCCCTAG[A/G]TATTTTTAAAAACAT	84708
rs183887798	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53609201	TGGAAAAATCATCTG[C/T]ATACAAAACCCCTGT	84708
rs183931099	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53648305	GATAGTAGCCATGCT[A/G]ATGGGTGGGAGGTGG	84708
rs183959324	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53602701	GGGAAGGCAATCAGG[A/G]TATTGTTTCAAGGAA	84708
rs183985559	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53643190	GGATCTTGCTCTGTT[A/G]CCCAAGCTGGAGTGC	84708
rs183988097	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53570035	GGTGGAGAGGATGTG[A/G]AGAAATACGAACACT	84708
rs183993610	snp	A/C	0.0244538	0.107838	intron-variant	LNX1	GRCh38.p7	4:53540709	CAAAAAACAAAAAAA[A/C]CCCCCTGTTATTATT	84708
rs183997224	snp	A/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53468108	AAGGTCGGGTTACCC[A/T]CAAAGGGAAGCCCAT	84708
rs184002268	snp	A/G	0.000399281	0.0141238	intron-variant, synonymous-codon	LNX1, LOC101928879	GRCh38.p7	4:53575835	GGACCAGCTACTAGG[A/G]GACCTAAACAGGAGC	84708
rs184015652	snp	C/T	0.00795532	0.062565	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53504884	GCATGGCTCGTGGCA[C/T]GCTAAAACAATTACA	84708
rs184020222	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53605923	ATCAGCTGGTGATTC[C/T]GTTTCCCAGAAGAGG	84708
rs184021664	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53585009	TCCAATTGTCTTCCT[A/G]GGTAGTCCAGATGGT	84708
rs184054961	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53625190	TTCTCAGCTATGACA[C/T]GAAAAGCACAAACAG	84708
rs184055133	snp	C/T	0.0119091	0.0762411	intron-variant	LNX1	GRCh38.p7	4:53645264	GCCATGACAGAGCTC[C/T]CCAGGAACATTCTAG	84708
rs184058244	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53629038	ACAATATACACTACC[C/T]GGGTGATGGGTGCAC	84708
rs184068192	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53545277	CTGGCCAGAGAAACT[A/T]CCCAATCATTACCCA	84708
rs184075663	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53520356	TCAGAATTCCAAAGC[A/C]ACAACCAGATGTGGA	84708
rs184086703	snp	A/C	0.00478085	0.0486577	intron-variant	LNX1	GRCh38.p7	4:53543408	GCCTGATATGTCATA[A/C]ACATTTGATAAGTAT	84708
rs184088699	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53578612	GAAGAAAAAGATTCC[C/T]TGATTTCACTGAGTG	84708
rs184094570	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53462249	GGAGAAGGAAAGGCC[C/T]AGCTCTTCTGTAAAT	84708
rs184102008	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53580165	TGATTAATAGAGGAA[A/G]AAGTCCACATAATGA	84708
rs184107290	snp	A/C	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53527217	TAAACATATGAATTT[A/C]AATGAACAGATATTG	84708
rs184110241	snp	C/G/T	0.00279258	0.0372817	intron-variant	LNX1	GRCh38.p7	4:53477367	GCTCCAGCATTTGCA[C/G/T]GGAGCCAGGCATGTA	84708
rs184110432	snp	A/C	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53562180	TCGCTCAGGATCAAG[A/C]AGTAAAAGCTTGGCT	84708
rs184110505	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498329	GAAAGAGGAGGTGGA[G/T]AAAGGGAATGAAGAG	84708
rs184115137	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53640046	TGTCTCAAAAAAAAA[C/T]AAAAATAAAAAAGAA	84708
rs184122838	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53497245	ACACAGGCCCAGCCA[A/G]AGCCCCCTATGTTGG	84708
rs184141922	snp	A/T	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53619799	TCAAACTGTTTTTCC[A/T]AAGTGGTTGCACCGT	84708
rs184145217	snp	A/G	0.00597247	0.0543191	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53599802	CCCGAGAAAACCTAT[A/G]CCTCTTATAGCTTTA	84708
rs184145509	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461882	TTTTAACTTAAGACA[A/G]TGCTTGAATATGTAT	84708
rs184167470	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53484759	GAGACAACTGCTAGC[A/G]TACAGTAAGAGTGTC	84708
rs184169968	snp	A/C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53492078	AGGCATGAGCCACTG[A/C/T]GCTTGGCTGAGGATA	84708
rs184195637	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53537386	AAGTTCTAGTCTTCC[C/T]TCTGTCTAATCTAGT	84708
rs184199788	snp	A/G	0.00398564	0.0444627	intron-variant	LNX1	GRCh38.p7	4:53561353	CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC	84708
rs184230028	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53526807	GTGAATTCCTTCGAC[C/T]TCTTCTGTTATATTG	84708
rs184256656	snp	A/G	0.000116267	0.00762363	intron-variant	LNX1	GRCh38.p7	4:53477030	GAGAGCACAAACAGG[A/G]ACTTCTGCTTAAAGT	84708
rs184302761	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53553507	TTCTAAGGTTTTCAT[C/T]TACAAGTCTCTCCAC	84708
rs184313098	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53522369	AATACTGAAGTGATT[A/G]CTAAAGTCTACTAAA	84708
rs184320116	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53541309	AAAACTACACTGACT[G/T]GGCAAGATCATGTCA	84708
rs184328706	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53518893	ATAAATGCCAGCTAC[C/T]GAGTAACTGCCATGA	84708
rs184335894	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53466031	TGTTTGTAAGAGGCA[C/T]TTATGATTCCATTGT	84708
rs184340340	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53481340	AATCACTCATTTCTA[A/G]GCAGACTGAAAAATT	84708
rs184345236	snp	C/T	0.00755907	0.0610114	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53503027	GCTCCGCCTCCCAGG[C/T]TCACATCATTCTCCT	84708
rs184405532	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53480245	GAATATAAGTTAAAA[C/T]GGAAATAATTACAAT	84708
rs184421607	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53595878	CTTCCTATTTTTTTT[C/T]CCCATGACATATTTC	84708
rs184422947	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53644302	GCTACTTGGGAGGCT[A/G]AGGCACGAAAATCGC	84708
rs184425971	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	LNX1, LOC101928879	GRCh38.p7	4:53576739	TTTCCACAAGAACAT[A/G]AAGACACACGAATAA	84708
rs184428217	snp	A/C	0.000399281	0.0141238	intron-variant, nc-transcript-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53523019	GGCTGAGCAACAGAC[A/C]CATTTGGGAAGATTT	84708
rs184432991	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53558655	ATTCTCTGTCAGAAT[A/C]ACAAAGAGCCTGGAT	84708
rs184435648	snp	A/C	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53541621	GACTTGAGACAAGAA[A/C]AATATAAGGCCAAGA	84708
rs184468204	snp	C/T	0.00279162	0.0372561	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53600851	TTTTCCTGCCTCAGC[C/T]TCCTGAGTAGCTGGG	84708
rs184493568	snp	G/T	0.00398564	0.0444627	intron-variant	LNX1	GRCh38.p7	4:53640859	TTGAAAATGAAGCTG[G/T]GTTTCAGGTTCGACT	84708
rs184528611	snp	A/T	0.00438332	0.0466095	intron-variant	LNX1	GRCh38.p7	4:53465673	GCCAAAGAACTTTTT[A/T]AAAATTCTGATACAT	84708
rs184546413	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53502740	AAATTAGAGTCAATC[C/G]TCTACTAACCTTGCT	84708
rs184590833	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53620204	TTATCTATCTACCTA[C/T]CTATCTATCTACTCT	84708
rs184604784	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53581442	TCCTCTTTGCTCACT[G/T]TATTAGTCCATTTTC	84708
rs184613329	snp	A/C	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53533046	CCTGTTATTAAGCAC[A/C]TATGCTCCCTAGGTG	84708
rs184632734	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53635947	CAGTGTGGGCTGATA[A/C]GGCCAGTGATGGGGA	84708
rs184638692	snp	A/G	0.00953873	0.0683987	intron-variant	LNX1	GRCh38.p7	4:53568801	CTTAAGCTGATAAGC[A/G]ACTTCAGCAAAGTCT	84708
rs184640256	snp	C/T	0.0821764	0.185298	intron-variant	LNX1	GRCh38.p7	4:53471185	CCTCAGAAATAATGC[C/T]GCATATCTACAACCA	84708
rs184640375	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53493063	AAACCTCCGCCTCCC[A/G]AGTTCAAGCAGTTCT	84708
rs184643917	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53616858	ATCTTTTAGCAAACA[C/G]CCTGGCTTGAAATGT	84708
rs184647164	snp	A/G	0.00318978	0.0398085	intron-variant	LNX1	GRCh38.p7	4:53550605	AAATGAAGTGGGGAG[A/G]AAATGGATGCTAAGG	84708
rs184651420	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53511309	GGGGCAGCTTGATTT[A/G]CAAGCATTAAAGATG	84708
rs184676839	snp	A/T	0.00279162	0.0372561	intron-variant	LNX1	GRCh38.p7	4:53554375	ATTGGTTTGGCCAAG[A/T]CGTTATAAACTATTG	84708
rs184683132	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53584639	ATCAAGGAAGAGTAG[C/T]GATCTCTTGATGTGA	84708
rs184704982	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53590146	GAAGAACAATAGGGA[C/T]CTCCAAACAGTAAGA	84708
rs184765852	snp	A/G	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53631128	AGGAAGTCGCCCATG[A/G]AGTTAAGGGATGCAG	84708
rs184779622	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53551053	TGTATGTCGCAGGTT[A/G]GGTTAGAGTCAGTTA	84708
rs184787637	snp	A/G	0.00676609	0.0577691	intron-variant, missense	LNX1, LOC101928879	GRCh38.p7	4:53576097	GGGGACTTGGCCAGC[A/G]TGGTATTTGGGAGCC	84708
rs184806441	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53537882	TTTGCTTCCTTTCAG[A/G]AAACGGTGTGGGGAG	84708
rs184820993	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507087	ATAATGGTACTAGCG[C/T]CTGAAGGTGAGGGTT	84708
rs184822129	snp	A/C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53616156	AACATGTGATGTTTG[A/C/T]GTTTCTGTGGGCTTG	84708
rs184839700	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53536994	TTTCTAATTACTTAG[A/G]AAAATCTACCTTTTT	84708
rs184844038	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53611607	TGTCTATAAACCCAT[C/T]GTATTAGGTTGGGGC	84708
rs184853130	snp	A/G	0.00795532	0.062565	intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53574671	GCTAAGTGGGCTCTG[A/G]ACACTTTGCCTGGGT	84708
rs184855550	snp	A/G	0.0142736	0.0832652	intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573423	TTAGAATTTTAAAAA[A/G]TCCCATAAACACATA	84708
rs184858743	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53650003	GGACTGCCCAAATAG[C/T]AGTTTTCACCCTGGA	84708
rs184864202	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53495925	GGAGGCACTGCATGA[C/T]ACATGTGGTAGTGAC	84708
rs184866198	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53553224	GTGATAATTTTCAAC[A/T]GGGAAAGTCAGGGTA	84708
rs184875347	snp	C/T	0.00993419	0.0697739	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53517102	TGCAAAGAGCACTGG[C/T]GGACAGGGTCTGGCA	84708
rs184880221	snp	C/T	0.00795532	0.062565	intron-variant	LNX1	GRCh38.p7	4:53468659	GATCTACCAAGCAAA[C/T]GGAAAACAAAAAAAG	84708
rs184895645	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53594664	TGGTTTTACCCCCCA[A/T]GATCAAACCCTTTTC	84708
rs184901973	snp	C/G	0.00358779	0.0422022	intron-variant	LNX1	GRCh38.p7	4:53636890	TGTAGTTTAAAACAT[C/G]TGTTTGGAGTGAAGG	84708
rs184908478	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53557343	AAATATGGGTGCTCA[A/G]GGCATGTTTCTTCGT	84708
rs184916508	snp	A/C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53533738	ATTTGGGAGGGTGCT[A/C/G]CTGGCATGTAGGGGG	84708
rs184929206	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53635300	CTGACGTTGTTTGAA[C/G]TAGATCCCCCCTTCC	84708
rs184945545	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53640521	GCAAGCATATGAAAA[C/T]ACATACATTTCATTG	84708
rs184949720	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53511722	TCTCCTTCCTGCAAA[A/C]CTTCTGAGTTCACTG	84708
rs184966655	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53488488	TAAAGTTGTGTGTGT[A/G]CACATGCAGAATAGA	84708
rs184973358	snp	A/G	0.00795532	0.062565	intron-variant	LNX1	GRCh38.p7	4:53546127	CCACATTTTTAATCA[A/G]TACAAGCTAAAGCTT	84708
rs184975464	snp	A/C	1.70142e-05	0.00291664	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507987	CCCATTTGACTCACC[A/C]CTAGTTCGGTTGCTC	84708
rs184979828	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53528515	ATTATTACAATATAT[G/T]GCTATAATTATTGTA	84708
rs184981283	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53466695	AGGAGATTATATCCC[A/G]CACCTGGCTCGGAGG	84708
rs184995386	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53532370	GCCCCGGCTACTCGG[A/G]AGGCTGAGGCAGGAG	84708
rs185036117	snp	A/C	0.00358779	0.0422022	intron-variant	LNX1	GRCh38.p7	4:53567685	ACACAAAAAACCCTT[A/C]AAAAAATTGATGAAT	84708
rs185053066	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53503474	ATCGAAGTACTTGGG[C/T]AACTAGGATGCATTA	84708
rs185062739	snp	A/T			nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53605203	ACATTGAAGAGCATG[A/T]GGAATGGGAATTGTG	84708
rs185096491	snp	C/G	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53511217	AGTCTCTTGGCTTAG[C/G]TTGAGCCAGAGACAG	84708
rs185107244	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53482144	TTGCTAATTCATTTT[A/T]AATTAATGGTTGTAC	84708
rs185135922	snp	A/C	0.00557542	0.0525036	intron-variant	LNX1	GRCh38.p7	4:53584073	ATCAGAGGGGTATGG[A/C]AAAGAAGCAAACTGA	84708
rs185150973	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53549587	GGTGTGATATTAGTA[C/T]TGTGCTCACATTTCT	84708
rs185167600	snp	C/T	0.00358779	0.0422022	intron-variant	LNX1	GRCh38.p7	4:53624025	TTCATGTAACCCAAG[C/T]TCTTAACTCCATCCT	84708
rs185238604	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53486096	GATCTAGGCAAATTC[C/T]GGACACACTGGTTAC	84708
rs185293347	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53641613	TTGGCATACATATAT[G/T]CCCATGAAATCATCA	84708
rs185422765	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53563515	AGAGATCCACAGTCT[C/G]GTTCTAGGTTAGCTT	84708
rs185432973	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53547483	GGTCAGTCTGACTGC[A/C]GAGCATGTGCCTTGA	84708
rs185437280	snp	A/C/T	0.00517822	0.0506191	intron-variant	LNX1	GRCh38.p7	4:53632568	ATTCATGTTCCCTGT[A/C/T]GGATCAGGCTAAAGC	84708
rs185450347	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53612824	CAGGAGTTTGAGGCT[G/T]CAGTGATCTGTGGTC	84708
rs185451261	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53621073	CCCAGGGAGCATTAC[C/T]CAGAGTGTGGTGCAC	84708
rs185453187	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53601628	CTCAATGCCATGTGG[C/T]TGCGGGGGTTTGGCA	84708
rs185467649	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53582091	ACTGTTAATTTTAGA[A/G]ACCTAAGAATATCAA	84708
rs185476728	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53650709	CCTCTGTCCCCTTCC[A/G]TGTCCCCCCAAGAAC	84708
rs185477201	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53542530	CAATACTCTGACTGA[A/T]GACCTAGGAGCAAGT	84708
rs185486236	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53522283	TTTCCTAAGGCCTGC[C/T]TCTCATCTCACTTTC	84708
rs185495900	snp	A/C	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53483330	TATAAATGACCCATT[A/C]TCGGGTATGTCTTTA	84708
rs185507428	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53560500	GTTACTACATGTAGA[A/C]CCTCTCACAGATGGG	84708
rs185508637	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53624449	GTAAGACATGTCTTT[C/T]GCCATCTGCCATGAT	84708
rs185512470	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53504390	TTCTTCACCTCTCTC[A/G]GCCTTCACAGAATCA	84708
rs185519699	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53525397	TGAGGCAGGAGAATC[A/G]CTTGAACCTGGGAAA	84708
rs185560711	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53581194	TATCAGTTGCAGCCT[A/G]AGGTCAAAGGAAAAA	84708
rs185576815	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53545920	TCAAGCAATTCTCCC[A/G]CCTCAACCTCCTGAG	84708
rs185585586	snp	A/C	0.00358779	0.0422022	intron-variant	LNX1	GRCh38.p7	4:53620151	ATTAATATTAATTTG[A/C]AGTTACTGGGTGTTT	84708
rs185641219	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53467432	TATAAAAATCAGAGC[A/G]CCTCTCCTCCTCCAA	84708
rs185655025	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53605425	ACTACCTTGTGTATG[C/T]GTGTATGGGGGTGGG	84708
rs185676430	snp	C/T	0.00755907	0.0610114	intron-variant	LNX1	GRCh38.p7	4:53644663	GGGAGCGGGATTCCA[C/T]GTCAGGTGACTTGGA	84708
rs185697990	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53562726	ACGAGGTGATTATAG[C/T]TAATAACAATGTATT	84708
rs185714479	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507668	AATCCTGCTTTTCTT[C/T]TTTGTTTCTGGGCTG	84708
rs185733921	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53600134	GTCAGTGCTCAGTGG[A/G]TAGGAGCAAATTACT	84708
rs185779997	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53646975	CTGTAAAAGGCAGGA[A/G]GTGTCCCGGCAGCCA	84708
rs185787850	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53608725	TAAATGCCCATCAAC[A/G]GTAGAATGGATAAAA	84708
rs185798934	snp	A/G	0.00438332	0.0466095	utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460684	ATAAACAATGTTGTA[A/G]AGTAATGAGAAATCC	84708
rs185814488	snp	G/T			intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53499615	CATTTTTAATGGAAT[G/T]AATTGCAGTTTTATC	84708
rs185829244	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53539497	CAGCCTTCCCAGTAG[C/T]TGGGACTACAGGCAT	84708
rs185840288	snp	A/G	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53486982	TCTTATAGCTGGAAG[A/G]AGTCTGGGAGCGTTG	84708
rs185847572	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53465040	ATTGTTATCAAGTTA[C/T]ATCCTAACAATTTAT	84708
rs185854997	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53528127	TAATCCTTTGTGTCC[G/T]CTCAGCGTATTTTCC	84708
rs185883828	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53642195	TTACTGCACTCCAGC[C/G]TGGGCAATGCAGAGC	84708
rs185948526	snp	C/G	0.00318978	0.0398085	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53520916	GCAGTGAGCCAAGAT[C/G]GTACCACTGCACTCC	84708
rs185952238	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53513868	ACTAAAGCATAAGGT[C/T]CTTACAACGATCTAT	84708
rs185969266	snp	C/T	0.00279162	0.0372561	intron-variant	LNX1	GRCh38.p7	4:53560878	TGATGTAATCCTAAT[C/T]AATACAATCCCTTGG	84708
rs185980047	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53473115	AAGAAAAGAAAATTG[A/T]TAACCAACCATATTA	84708
rs185980494	snp	A/C	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53478405	AGTGGAACCTGGTCT[A/C]GTATCTATACTCAAA	84708
rs185989832	snp	G/T	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53618463	GGCTTTCTACTCAAA[G/T]AACAAAAACTGGAAA	84708
rs185992615	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53493617	CATAACCAGATCTCA[A/G]GTGCAGGCAAATTTA	84708
rs185999293	snp	C/G	0.00279162	0.0372561	intron-variant	LNX1	GRCh38.p7	4:53542931	CAGGTGCCAGCTCCT[C/G]TAACGTGGTTCTCAC	84708
rs186004275	snp	G/T	0.000798403	0.0199641	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53598489	CCTCCTGCCTTGGCC[G/T]CCCAAAATGGTAGGA	84708
rs186007501	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53578395	AGTCTATGGCTCTTA[C/T]GCTGCAAACCTGTAC	84708
rs186025953	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53638412	AAATTGAATTGTAAC[C/G]CCAAACTCAATGCTC	84708
rs186062320	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53575197	ATGTTGGCCAGGCTG[A/G]TCTTGAACTCCTGGC	84708
rs186162401	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53632991	GTCCTAAGACAAGAC[A/G]TCATTAGTGTGTGAG	84708
rs186175038	snp	C/T	0.00199481	0.0315187	upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53592877	AAGGAAGAGAAATTG[C/T]AGTCGAGGGCGGGGT	84708
rs186198735	snp	C/T	0.0189856	0.0955633	intron-variant	LNX1	GRCh38.p7	4:53467066	TGTGTCCCTGACCCC[C/T]GAGTAGCCTAACTGG	84708
rs186203297	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53555054	AAACAAGGAATACAG[A/G]GCAAGCTTCCCCCAG	84708
rs186230206	snp	G/T	0.00279162	0.0372561	upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53592546	ACCTGAGGAAACTGT[G/T]GATTCCCCGTCCCGG	84708
rs186261997	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53489311	GTTTATTTTTCCCAG[C/T]AGACTATAGCTCCAT	84708
rs186294547	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53607404	GAATATAGCTAACCA[A/G]GGAGGGGAACAATCT	84708
rs186301807	snp	A/G	0.0263992	0.111815	intron-variant	LNX1	GRCh38.p7	4:53613401	AGGATGTGCAGTTTC[A/G]TTACATAGTAAACAT	84708
rs186335430	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53555909	TTAAGTGGTATAAGG[A/T]CCTTCCTTCAATTAG	84708
rs186351320	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53651504	TTCTGGATTTTCCAG[A/G]AGAGTTCCAATTTCT	84708
rs186374067	snp	C/T	0.00438332	0.0466095	intron-variant	LNX1	GRCh38.p7	4:53578139	TTTGTCTCCCAGAAT[C/T]TTTCTTGATTATGGC	84708
rs186376272	snp	A/G	0.00795532	0.062565	intron-variant	LNX1	GRCh38.p7	4:53493993	TCTGTCTCTTGCCTC[A/G]TCTATGGCTGCTTTT	84708
rs186401957	snp	A/C	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53617763	ATGTTATTGACTAAA[A/C]CTGTAACAACTGGGT	84708
rs186416678	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53469282	AAATAAAGATGTTCT[G/T]TGAAACCAACGAGAA	84708
rs186424876	snp	A/C	0.00557542	0.0525036	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53515387	GGAATTGTGGGATTC[A/C]CTCACACCACCCTGA	84708
rs186427722	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53586733	ACAAGAGTAAACAGA[C/T]GATTGTAAAAACTGC	84708
rs186430426	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508603	ACCATGAAAGCCCTT[A/G]GTCACACCCTCACTC	84708
rs186432333	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53535282	TTGTTTTGGATGCTT[A/C]AGCCATGACTCTTTT	84708
rs186433713	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53617453	TTACTTCTCAAGAGG[C/T]TTAGAAACCCAAAGC	84708
rs186433748	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53570838	CGAGACCATCCTGGC[C/T]AACACAGTGAAAACC	84708
rs186439037	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53551734	CACCCGCTTGGCCCT[C/T]TTCTAAGTGTACTTC	84708
rs186456738	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS2	GRCh38.p7	4:53591204	GCCTGGGAGAAGTTT[A/G]TTGTGCAACTAGAAT	84708
rs186460357	snp	A/G	0.00676609	0.0577691	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53499395	AAATCCTGAGCCCAG[A/G]TGATCCACCCACCTC	84708
rs186463563	snp	C/T	0.0236746	0.106192	intron-variant	LNX1	GRCh38.p7	4:53469895	AGATGGATTCACAGC[C/T]GAATTCTACCAGAAG	84708
rs186465583	snp	A/C	0.00199481	0.0315187	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53520804	CCATCTCTACTAAAA[A/C]TACAAAAATTAGTTG	84708
rs186466474	snp	A/C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53491217	TGCAGAGGGAGTTAA[A/C/G]AAGTGTAACATGAAA	84708
rs186469164	snp	C/T	0.00716266	0.059414	intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53575004	TTTTTTCTTTTTAGA[C/T]GGAGTCTTGCTCTGT	84708
rs186470917	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53539083	TAAAGGTTTTTGTTT[C/T]TTCCTTTAGGTTAAA	84708
rs186473972	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53554558	CGAATGATACATGTT[A/T]TAAAATAATTCCTGG	84708
rs186479896	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53631677	ATCAGAATTTCCAGG[A/G]TATGAGACCCAAGCA	84708
rs186494681	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53611762	TATATGAATGAAAAA[C/T]ATAAAAGGTAAAGTA	84708
rs186505242	snp	G/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53472273	ATTCTCACTCATAGG[G/T]GGGAATTGAACAATG	84708
rs186522542	snp	C/G	0.000399281	0.0141238	intron-variant, missense	LNX1, LOC101928879	GRCh38.p7	4:53575374	AAGTTTTTCAACATG[C/G]TTGCTTTGCATCTAG	84708
rs186598932	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53534687	TTTTGGTCACTTGGC[A/G]TAAAACAACCTATTT	84708
rs186603131	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53504630	GCCTAGCTTTCAGCC[C/T]ACCTTAGCTTTCAAT	84708
rs186615845	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53637746	CCAGTTTCTGAGATA[C/T]TAAAATGTAAAAGAA	84708
rs186621903	snp	A/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53597186	TTTGCAATGCTAGCT[A/G]CACTTGTCACTCTCC	84708
rs186662967	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53470345	GGACGTATCTCAAAA[C/T]AATAAGAGCTATCTG	84708
rs186664561	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53491539	AAGAAGTTGCTCAGT[C/G]AATAATCACTGAACA	84708
rs186730448	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53493385	CTTGGAACTGGGACA[A/C]CACCAAGTGGCACAG	84708
rs186808878	snp	A/C	0.000798403	0.0199641	upstream-variant-2KB	LNX1	GRCh38.p7	4:53654260	AAGGTAATTTATAAC[A/C]GTCAAATTGGCCTTT	84708
rs186827018	snp	A/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53634826	TTTTTTTTTCTTTTT[A/T]AATTTTTTATTATTA	84708
rs186832854	snp	A/T	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53484273	GCACACAACTCACTC[A/T]CTCTCAGGAACTAGG	84708
rs186850713	snp	A/G	0.00795532	0.062565	intron-variant	LNX1	GRCh38.p7	4:53551309	TCAGGCAACCATCAG[A/G]TGATGGTCAGGCAGT	84708
rs186873575	snp	G/T	0.00318978	0.0398085	intron-variant	LNX1	GRCh38.p7	4:53606509	AAACAGAACAAGACA[G/T]ATTCACAGCCAAATT	84708
rs186891479	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53548238	CCCCATTCCTTCCAA[G/T]ACCAACTCCACAGAC	84708
rs186896183	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53570570	CCTAATGCTAAATGA[C/T]GAGTTAGTGGGTGCA	84708
rs186906550	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53645905	TTCATACTGATTACT[A/G]TTTCACTCAGAGTTT	84708
rs186916214	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53465779	TTGAAGTTGGTTTTC[A/G]TATCACTAGTTATGA	84708
rs186916452	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53510004	ACAATTGGATATTGA[A/T]GAAGTACATATTCAT	84708
rs186918106	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53602740	ACGTGTTGGGTGATA[A/G]TTCACAAGGCTTCAG	84708
rs186925818	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53582780	ATGTGGCAGAATGGT[C/T]GCTTAGTTTCAAACT	84708
rs186927969	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53531051	GTGCCTATGGTCTCA[C/G]CTACTCAGGAGGCTG	84708
rs186929874	snp	A/G	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53564875	CCTTTCCTAATCAAA[A/G]AAAGGGGTGACAGAC	84708
rs186936831	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53465116	TTGGCCATTGAAAAA[C/T]ATCTTGCATTTTTTT	84708
rs186965296	snp	A/G	0.00478085	0.0486577	intron-variant	LNX1	GRCh38.p7	4:53539966	CATGTGGTTAGAACT[A/G]GAAATTCAGTATTTT	84708
rs186983580	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53583809	GTTCCTTCTCTTGAC[A/G]AGATTTTACCACCTT	84708
rs186995419	snp	A/G	1.64776e-05	0.00287028	synonymous-codon	LNX1	GRCh38.p7	4:53478686	GCCGAGAGATTCACC[A/G]GGGTCTTTTTGGATA	84708
rs186998763	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53626897	GTCTGAAATGGAAAT[A/T]GAAGCTAGAAGCATT	84708
rs187004406	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53501326	GACAGGATCTCACTC[A/T]GTCACCCAGGCTGGA	84708
rs187007385	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53623106	TCAGGATTCATGATC[C/T]TGGACTGATCACTTG	84708
rs187014497	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53643837	GAAGTCAAACCATGT[A/G]AAAAGTTTGTTGGGG	84708
rs187014760	snp	A/T	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53521323	AGGTGTGGGGGAAGG[A/T]GAAAATCATTCCCAG	84708
rs187029183	snp	C/T			nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53604251	ATTAGCACCTAAAGC[C/T]TGTATATTCATTTAT	84708
rs187077918	snp	A/G	0.00358779	0.0422022	intron-variant	LNX1	GRCh38.p7	4:53585942	GTGAATGCTCCCAAC[A/G]ATCCTTTCCAACACT	84708
rs187100269	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53482493	AGATAAAGAAAATGT[C/G]GTATGTATATACCAT	84708
rs187100903	snp	C/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53526555	TAACAGTGATGAGAG[C/G]CTTTTCCTTCCAGAC	84708
rs187112847	snp	A/G	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53523819	TTGCTAATTATCCTA[A/G]AATACTCAATGAAGC	84708
rs187123783	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53625730	GAGGATTGCTTGAGC[A/C]TGAGAGGTTGAGGCT	84708
rs187155097	snp	C/T	0.00716266	0.059414	intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53560064	TATCCCTTCTTTCCT[C/T]CTATACTATTAGAGA	84708
rs187178810	snp	G/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53596247	ATTTCTCTCACAAAC[G/T]TACAACCTGTGTGTT	84708
rs187182927	snp	C/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53468345	CTCCTGGAGGAAGCA[C/G]TAAATATGGAAAGGA	84708
rs187183592	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53509468	TGGCAAGATGGAAGG[C/T]CCTATTGTCTAGATC	84708
rs187192982	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53485341	TTTTGGATGAGGAGT[A/G]GCCACATGATCTAAG	84708
rs187200845	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53646640	GAATTTTTATATGAA[A/G]TCTCCTGATTGTTAG	84708
rs187211454	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53547779	TACAGGAAAATATGA[C/G]AGAATAAGAAGAAGG	84708
rs187226432	snp	C/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53544802	CATGATATAGTCTGT[C/G]AGTCCTCACAGTAGC	84708
rs187226708	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53587529	ATAGTTGTATGCTAC[C/T]GGGAAGTCCATGAAT	84708
rs187246821	snp	A/T	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53506334	AAGAGCTCAATTTTT[A/T]AAAAAAGCTGTTACT	84708
rs187249824	snp	C/T	0.00358779	0.0422022	intron-variant	LNX1	GRCh38.p7	4:53579766	TCTCCTTTCAATGCA[C/T]CCTGGCTTTATAGAA	84708
rs187250222	snp	C/T	0.00914312	0.0669923	intron-variant	LNX1	GRCh38.p7	4:53526973	AATAGAAATGAAACA[C/T]CTAAATGAAGGGTGA	84708
rs187264901	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460113	TACACACACTCTTCA[C/T]TGTGGCACAAATTTA	84708
rs187268762	snp	A/C	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53650353	GTGTCAGGGCCTAAG[A/C]AGGGTGCGGAGGGCA	84708
rs187270425	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53582547	CCTACTGTATTCATG[C/T]TTGCTTTGAATTTTT	84708
rs187276065	snp	C/T	0.00199481	0.0315187	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53503908	GGAGGCCGAGGCAGG[C/T]GGATGACCTGCGGTC	84708
rs187284713	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53473928	TCCCTGAAAAGCAGC[C/T]ACAAAATAATAGAAC	84708
rs187297500	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53633561	AGTTTTTGCCAGCTA[A/G]GCAGAGTTAGGTTGG	84708
rs187301989	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime	LNX1	GRCh38.p7	4:53652292	TTTCCAGTGTTCTTC[A/G]TCCCAGCTATGCATG	84708
rs187310811	snp	A/C	0.00279162	0.0372561	intron-variant	LNX1	GRCh38.p7	4:53621872	GACCTTTCATTTCAC[A/C]CCCACCGGATTTGTT	84708
rs187341306	snp	A/T	0.02016	0.0983543	intron-variant, downstream-variant-500B	LNX1, LOC101928879	GRCh38.p7	4:53577778	AGAATCCTAGCTTTT[A/T]AAAAAAACTTGCAAA	84708
rs187366949	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53542180	GATATGCAATTGTCA[A/G]CTTGAAAAATTGGGA	84708
rs187384394	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53478086	TACATGAGCTTAAAG[G/T]AGTGAAATAATTTTC	84708
rs187404912	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53529482	ATTCACATAAGACTG[C/T]GATGCCTTGGAAATG	84708
rs187455160	snp	C/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53602351	TGTCAGACCACCATC[C/T]GATCTGACACCAGTG	84708
rs187463200	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53536601	GGGCCTCTGTGTCCC[C/T]GGTTTGGTGCTTCCA	84708
rs187483676	snp	C/T	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53475558	CACCCTCAAGAAAAA[C/T]GTACTAAAACTAAAC	84708
rs187487986	snp	A/G	0.00676609	0.0577691	intron-variant	LNX1	GRCh38.p7	4:53495780	AACTCCTGACCTCAT[A/G]TGATACACCTGCCTC	84708
rs187489974	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53516778	CCAGTCCATCTACCT[A/C]CTTCTGGGGTTCAGT	84708
rs187499998	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53564156	AAAGTGCATCTCATT[A/G]TGAGCTGAGTGTTCA	84708
rs187538762	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53619525	GTCATGCTTATCCAT[A/G]TTAGAGAAAAAAGTA	84708
rs187541195	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573537	ATCATTTCATTGGTT[A/G]GAAGCCCTCAGGAGA	84708
rs187545931	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53553315	GGGAGTTTGTCAAGA[A/G]TGAAAATGGGGTGGC	84708
rs187562673	snp	A/G	0.00795532	0.062565	intron-variant	LNX1	GRCh38.p7	4:53537111	AGTGGTAGTGGGGAC[A/G]GTATGAGTACTGATT	84708
rs187565593	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53610023	AGATTTGAAAATGGA[C/T]ATTTTCTCTAAAGTC	84708
rs187568722	snp	C/T	0.00358779	0.0422022	intron-variant	LNX1	GRCh38.p7	4:53589165	GACAACTGGACATTT[C/T]CCCCGAAAGGCCCAT	84708
rs187570013	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53642067	TCTCTACAAAAAATA[A/G]AAACATCAGCCAGGT	84708
rs187573322	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53638892	ACTATTGGTGGGAAG[A/G]CAAATTAGTTCAGCC	84708
rs187619234	snp	A/G	0.00517822	0.0506191	intron-variant	LNX1	GRCh38.p7	4:53629720	TTTAGGGTAATCAGA[A/G]GTGGTAGGGTGGATG	84708
rs187641060	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53463405	TGTTTTGAGTATTTA[A/C]CTTTATTGCCGCAGC	84708
rs187652746	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53580807	TTGCTATCTGAGGAA[C/T]GTGGGGCTCTCTTAT	84708
rs187676118	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53619812	CCAAAGTGGTTGCAC[C/T]GTTTTACACACCCAG	84708
rs187677713	snp	A/C	0.00597247	0.0543191	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53599933	GCATTGCACCTTGGG[A/C]AGAACTTGAAAAAGA	84708
rs187689981	snp	G/T	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53541169	AAAAAAGAAAGAAAA[G/T]AAAAGAAAGAAAGAA	84708
rs187722355	snp	A/G	0.00438332	0.0466095	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53502951	TTTTTTTTTTTTTTA[A/G]ATGGAATCTTGCTCT	84708
rs187727286	snp	C/G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53643229	GATCATGGCTCACTG[C/G/T]AGCCTCAAATTCCCA	84708
rs187732168	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53615685	GTTGGTAATACAACC[A/T]TGCCTTATTAATACA	84708
rs187737302	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53517973	CCAACCACACACGGC[G/T]TCCCCTCATTAGCCC	84708
rs187752883	snp	C/T	0.00119737	0.0244387	intron-variant, missense	LNX1, LOC101928879	GRCh38.p7	4:53575984	TGGCAGGCATGCACA[C/T]GCTGCTCCAGCAGGC	84708
rs187772211	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53639803	TTGGGAGGCCGAGGC[A/G]GGTGGATCACTTGAC	84708
rs187779204	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53522047	CAATCCTTCCATCTC[A/G]ATCTCCCAACTAGCT	84708
rs187812597	snp	A/C	0.00398564	0.0444627	intron-variant	LNX1	GRCh38.p7	4:53556582	TTCATAATCTCTGCC[A/C]TTGTCTGTTTGTCTA	84708
rs187838593	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53540366	CCAGCCTGAGTGAGA[C/G]TGAGACCCTGTCCCC	84708
rs187840799	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53614669	AGGGTCTAATAAAAG[A/T]AATAAGCAGCCAAGA	84708
rs187848648	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53593785	CAGGTGCTACTTATT[A/G]TTCTGAGCACTTTAT	84708
rs187852798	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1, LOC101928879	GRCh38.p7	4:53575553	CACACAAGTAGGAGC[A/C]CAGTGCAAACTAGGG	84708
rs187870767	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53468180	GAAGAGAGTGGGGGC[C/T]AATATTCAACATCCT	84708
rs187888420	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53484831	TCATTTCACAAAAAC[C/T]AGAAAATCCTTCTGA	84708
rs187936701	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53491702	ATATACACATAGATG[A/T]TCATAATTTGACTCC	84708
rs187950102	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53532339	AAATTAGCCGGGCGT[A/G]TTGGCACGCACTGTA	84708
rs187970182	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53522320	GATGCTTCATAGTGA[C/T]CTCTCCCCTCTCAAT	84708
rs187993300	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53556852	CATGGGTGGTAGCAC[C/T]ATCTAATGTGACCAG	84708
rs187994192	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53516197	CAGTAGGCCATGACT[A/G]GGCTACTGCACTCCA	84708
rs187999453	snp	C/T	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53480849	AAAGAAAAGGGCATT[C/T]CCTACTTTCTGTTGC	84708
rs188022061	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53594608	TCAACTCAGAAGGAA[C/T]TTTGGAATCTTGAAG	84708
rs188027835	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53474525	TAGAATACACAAGAA[A/T]TTGATAATGGTGATC	84708
rs188030174	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53622210	CTTTGGAAAGATGTA[C/T]GTATGTCATATGCCA	84708
rs188049345	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53552267	TACTTTGAAAAGCGA[A/G]TCCCAAACTAACTGT	84708
rs188055510	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53610937	GAAATGCAAAATTAT[A/G]AAAGATCAGAAAGCA	84708
rs188059147	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53563412	GGTCTCCAGAGGTAT[C/T]AACTACTTCTTAAGT	84708
rs188070408	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53546802	CAAGGAGCTAAATAG[C/T]TGAGGAATGAAGGCT	84708
rs188079564	snp	A/T	0.00874735	0.0655527	intron-variant	LNX1	GRCh38.p7	4:53528951	AGGCTACCCATAAAA[A/T]AAAGCCATCACAGAG	84708
rs188083426	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53649159	ATGCCAAAATCTATT[G/T]GTTTAAATTTCTGTC	84708
rs188086422	snp	A/G	0.0142736	0.0832652	intron-variant	LNX1	GRCh38.p7	4:53548991	TGAACACACAGAAGG[A/G]AATGACCGACACTGG	84708
rs188093542	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53630839	GCTAATTCAGTGTTT[A/G]CAGTGATTTTAAAGA	84708
rs188095707	snp	A/C	0.00119737	0.0244387	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53600904	CCTGGCTAATGAAAC[A/C]CCATCTCTACTAAAA	84708
rs188103973	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53581851	ATGTTTGATCATTTC[G/T]CTTAACTAAGTGATG	84708
rs188224933	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53510514	TCCTGGCTTGAATTC[A/G]TGAGGTTTTACTGTA	84708
rs188229812	snp	C/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53467873	TGTCTGATTGGTGTA[C/G]CTGAAAGTGACGAGG	84708
rs188252163	snp	C/T	0.00557542	0.0525036	intron-variant	LNX1	GRCh38.p7	4:53470693	ATTCTTATACACCAA[C/T]AACAGACAAACAGAG	84708
rs188259201	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53493168	GAGATGGGGTTTTAC[C/T]ATGTTGGCCAGGCTG	84708
rs188264477	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53494529	TCAAGATCTTCCTCC[C/T]CTGAGGAATTCACAG	84708
rs188271669	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53511365	CATTGGCCAGGACAA[A/G]AACATACGGTAAACC	84708
rs188284219	snp	A/C	0.00318978	0.0398085	intron-variant	LNX1	GRCh38.p7	4:53535940	GGGAAGCTCAAATAC[A/C]AAAGGATTGGACTTA	84708
rs188289778	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53624039	GCTCTTAACTCCATC[C/T]TTTTGCTTGCCTCTC	84708
rs188299413	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53584326	GTGGGAGTTCCTGTA[A/G]GGAATTCCATTTCAT	84708
rs188314134	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53550643	CTGTATTCCACTCAC[C/T]CCCGACTCATTCACC	84708
rs188324928	snp	C/T	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53571563	GCAAGGAAAGGGATT[C/T]TCCCCTGAAGCCAAC	84708
rs188328341	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53533090	ACATATCAACACATG[G/T]CATAATTGTGTTTAT	84708
rs188330001	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53624492	CCAGCCACATGCAAC[C/T]GTGAGTCCATTAAAC	84708
rs188332185	snp	A/G	0.00953873	0.0683987	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53605676	TATAAGTGAAATCAC[A/G]CAGTATTTTTCTTGT	84708
rs188341202	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53599193	TCCCAGACAGTTATG[A/G]CATTCTAAGTCACAG	84708
rs188348033	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53584853	GCTAGTGCTTCCCAC[A/G]TTACTTTGACCTTTG	84708
rs188410030	snp	A/C	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53606009	CTTGCCAATTCTTAT[A/C]ATTCCTTGTCTTTAT	84708
rs188442629	snp	A/C	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53645705	TCTACACTGCATTAT[A/C]TTGGCCTCTCACATG	84708
rs188444769	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53625450	TGCACAAAGGGTCAA[C/T]AAGCACATGAAAAGA	84708
rs188505825	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53572754	TCAGCCATCAGCAGC[A/G]GCAATCACACCAGAA	84708
rs188507136	snp	A/G	0.00279162	0.0372561	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53503345	CAGCTATAGCCTTTC[A/G]AAATTTATTTCTTAA	84708
rs188515422	snp	A/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53522896	TTTATTCTTTCAATC[A/T]TTTTTCTATGCATAG	84708
rs188517463	snp	A/G	0.00874735	0.0655527	intron-variant, missense	LNX1, LOC101928879	GRCh38.p7	4:53576116	TATTTGGGAGCCAGC[A/G]GCCCCTCCTTGATTC	84708
rs188523305	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53541319	TGACTTGGCAAGATC[A/G]TGTCAAAAAAAAGAG	84708
rs188527288	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53557724	GACAGCTAAGCATGC[C/T]GTTTTAAACTGCTGG	84708
rs188544110	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53609152	TGACAAAAACAAGCA[A/C]TGGGGAAAGGACTCC	84708
rs188565834	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53648056	TGTGAATAATGCTGC[C/T]ATAAATATGGGAGTA	84708
rs188574139	snp	G/T	0.000399281	0.0141238	nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53605288	CTTAAAAAGAAATTT[G/T]AGTGTGTTATCGTCT	84708
rs188589801	snp	C/T	0.00398564	0.0444627	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53598898	TCAATATGACAAAGA[C/T]GGAAAGAATCTCTGC	84708
rs188604904	snp	A/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53644476	AAAGTGACTTAAGCT[A/T]GACTGATGTATTATA	84708
rs188605707	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53489188	AATGAGCTAAAAGCA[A/G]TCAGTCTGGCCAAGG	84708
rs188611636	snp	A/G	0.000399281	0.0141238	synonymous-codon, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508008	TCGGTTGCTCCGGCC[A/G]GAGTCCACTGGGCTG	84708
rs188638530	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53466194	TGGAATCACTAATAT[C/T]GTACTGTTTTCAGAA	84708
rs188640593	snp	C/T	0.00120482	0.0245144	missense	LNX1	GRCh38.p7	4:53481811	TCAGGGCTCCGCTGC[C/T]GAACCTGGCGGGACA	84708
rs188708315	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53467910	GAACCAAGTTGGAAA[A/G]CACTCTGCAAGATAA	84708
rs188732339	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53526896	CCACAGAAGGCTCAC[A/G]ATGTTTATAAAATTA	84708
rs188751408	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53561382	ACAGGCATGCACCAC[C/T]ACACCCAGCTAATTT	84708
rs188757992	snp	G/T	0.00199481	0.0315187	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53462012	ATCCTTTGAATAATC[G/T]CAATGAAAGCAGTTT	84708
rs188783222	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53479622	GAGGAGAGTTACGTA[A/T]GAAAGAGATGACTTT	84708
rs188797809	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53552690	AAAAATTAGCCAGAC[A/G]TAGTGGCAGGTGCCT	84708
rs188819089	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53628011	GGAAATCATGGATAT[C/T]GGTTTACAACACTCC	84708
rs188825583	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53588110	AACACTCACTGAACA[C/T]TTAAAATATGCCAGG	84708
rs188866850	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53549839	GTCAACCAACATGAA[A/G]CGGTCAGTGAGATTC	84708
rs188874525	snp	A/G	0.0107246	0.0724382	intron-variant	LNX1	GRCh38.p7	4:53578866	AGAAACAGATTATGA[A/G]ATAATTGACTGAACA	84708
rs188900198	snp	A/G	0.00478085	0.0486577	intron-variant	LNX1	GRCh38.p7	4:53619048	GAGCCACTGCACTCG[A/G]CCTCACTTTAGTCAC	84708
rs188929299	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53648591	GTGTCCTTTGGTGCC[C/T]AGACATTTTTTATTT	84708
rs188978208	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53595924	TGATTGAATGCCACA[A/G]TTAAAATGGACATAT	84708
rs188980353	snp	C/T	0.00438332	0.0466095	intron-variant, utr-variant-3-prime	LNX1, LOC101928879	GRCh38.p7	4:53577054	CACAGAAGGCAAAGA[C/T]AGAGGGTGCAGGAGG	84708
rs188992746	snp	C/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53558839	ACCTTTGAAATGGAG[C/G]TAATTATGCCTTACC	84708
rs189001093	snp	C/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53636147	AGAGTGGAAATCAAA[C/G]AGGGATCTCAGAGAC	84708
rs189005365	snp	C/T	0	0	intron-variant	LNX1	GRCh38.p7	4:53476045	CTCACACCTGTAATC[C/T]CAGCACTTTGCCAGG	84708
rs189012513	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53616912	TTTAAACTAAGAAGT[A/G]TTAAGCATAGTCATT	84708
rs189021385	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53543450	TTATACTCTTCCCAG[A/G]AATGAATGTTTTCTT	84708
rs189053889	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53505191	GACAGCACCTAGGCC[A/G]GTGCCTTACATATAA	84708
rs189068278	snp	A/C	0.00119737	0.0244387	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53501986	TCCCAGGTGTGTTCA[A/C]TACCCCCAAATCAAG	84708
rs189098888	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53620415	GCAAGCCCTGCAGGG[A/G]ATTCTAATGCAGGCT	84708
rs189100257	snp	A/T	0.00795532	0.062565	intron-variant	LNX1	GRCh38.p7	4:53465481	TTTTCTGAAGGAGGC[A/T]CTGTATTAAGTTACA	84708
rs189155094	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53532863	CAAGGAACACTGCAG[G/T]CTGCCCAGGAAGTTG	84708
rs189157361	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53486993	GAAGGAGTCTGGGAG[A/C]GTTGCACTGTGACCT	84708
rs189171920	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507828	GAGGTACTTGCGGTT[C/T]CATTTCACTTTGGCG	84708
rs189179975	snp	A/C	0.00398564	0.0444627	intron-variant	LNX1	GRCh38.p7	4:53617474	AACCCAAAGCTGTAA[A/C]CACAGCTGGGGAAAC	84708
rs189185713	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53477904	TCAGCAGCTGTACTT[A/G]GGAAACTTCACAGTT	84708
rs189189345	snp	C/T	1.65562e-05	0.00287712	missense, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498669	TCTCCTGGCAGTAGC[C/T]GGCCGTCTCTGGCGA	84708
rs189196533	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53644855	CATATTTAGTCAGAG[A/T]AAGGGAGAGATGTGG	84708
rs189219889	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53554444	TAAATTGGACACAGG[G/T]TTGTTGTTTTGTTTT	84708
rs189237133	snp	A/G	0.0103295	0.0711199	intron-variant	LNX1	GRCh38.p7	4:53562321	CAACTCAATAAGTCC[A/G]TCACCACCCTGGGAA	84708
rs189253594	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53520399	TAATGAGGGATGGTC[A/G]AGGGCTTGGGCACAG	84708
rs189260442	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53538612	TGCTTAAACCTAGTA[A/T]CATGGCATGCATTTG	84708
rs189276220	snp	G/T	0.0182019	0.0936463	intron-variant	LNX1	GRCh38.p7	4:53471347	AAATTAATTCAAGAT[G/T]GATTAAAGACTTATA	84708
rs189297046	snp	A/G	0.00795532	0.062565	intron-variant	LNX1	GRCh38.p7	4:53468660	ATCTACCAAGCAAAT[A/G]GAAAACAAAAAAAGA	84708
rs189324916	snp	A/T			utr-variant-5-prime, upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53591544	GACGGCATTGGTCGC[A/T]CCAGACCAGGAAATG	84708
rs189326123	snp	C/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53542329	TGTTGTTGTAATTAA[C/G]AATACAAAGGGATGG	84708
rs189327421	snp	C/T			intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53575066	TGCTCACTACAACTG[C/T]CACCTCCCAGATGCA	84708
rs189345972	snp	A/G	0.449218	0.151037	intron-variant	LNX1	GRCh38.p7	4:53471050	caatcctaagccaaa[A/G]gaacaaagctggagg	84708
rs189347083	snp	A/G	0.00636936	0.0560724	intron-variant	LNX1	GRCh38.p7	4:53631875	CCTTTTTTTTTTTAA[A/G]TCCTTGAGAATCCTT	84708
rs189349186	snp	C/G	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53650547	TGGAATTGGAAGTAT[C/G]AATTTATGGTTTTCT	84708
rs189354271	snp	A/G	0.0023933	0.0345097	intron-variant, downstream-variant-500B	LNX1, LOC101928879	GRCh38.p7	4:53577863	CTGTGCTAATCAAGT[A/G]AGGTTTTTATGTTTT	84708
rs189360326	snp	C/T	0.0023933	0.0345097	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53504133	GAGCGAGCGAGACTC[C/T]GTCTCAAAAAAAAAA	84708
rs189366700	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53612124	AGGGTTGAGAAACTC[A/G]GAAATATCCTCAAAT	84708
rs189375432	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53574354	AATCATTTGGGTAAT[A/G]TCTGGGAAATGCCTA	84708
rs189379931	snp	C/T	0.0119091	0.0762411	intron-variant	LNX1	GRCh38.p7	4:53534222	TTAATTATTCCACCA[C/T]TGCCTTCACGGCTTT	84708
rs189400182	snp	C/T	0.00159617	0.0282053	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53595119	TCATGAAGAAAGGAA[C/T]ATGAATTGGGCCTTG	84708
rs189407468	snp	C/T	0.00279162	0.0372561	intron-variant	LNX1	GRCh38.p7	4:53492584	TAAAGAGCTCATTCT[C/T]TCTGCTGTGCATAGA	84708
rs189409748	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53493401	CACCAAGTGGCACAG[C/T]TCAAAAGCTAAGGTA	84708
rs189411350	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53511295	TGGTGACTAATACTG[A/G]GGCAGCTTGATTTAC	84708
rs189422545	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53641172	GAGGAGATCCAAGCT[G/T]CTTGGCCACTTTCTC	84708
rs189440523	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53635676	GCAACTCATGAAAAA[C/T]AAGCCATTTTATATA	84708
rs189466240	snp	A/G	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53636914	GTGAAGGTGTTATAC[A/G]CTTATCTTGTATGCA	84708
rs189481107	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53596309	CTGTGGACCTACAGT[G/T]TAGGAGGAAACACTT	84708
rs189538096	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53541659	CTGTTTCAATTAAGC[G/T]CAGCAGAAAAAAATA	84708
rs189633179	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519312	AAACACATAGCATTT[A/G]AGGTGGGAAACAGGA	84708
rs189644651	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53560088	TTAGAGAAGTGACAT[G/T]TTATAGTCTTATCCT	84708
rs189652021	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53524816	TGCTTTCCAAGAGGC[A/G]TGCTAGCAGGAGATG	84708
rs189658264	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53512099	CAAATTCATATGCTC[G/T]TCAGGTGAGAGAATG	84708
rs189663014	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53553640	GAAATTCAAAAAGAA[A/T]GTTCATGGAGGTCTG	84708
rs189665139	snp	A/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53477145	TAGCAAATGGTAAAC[A/T]GTGTGTGCATTCCAA	84708
rs189683977	snp	G/T	0.00755907	0.0610114	intron-variant	LNX1	GRCh38.p7	4:53551108	AATCCTTGGTTCTAA[G/T]AGCTTGGTGTGTTCT	84708
rs189688218	snp	C/T	0.0193772	0.0965046	intron-variant	LNX1	GRCh38.p7	4:53472385	GAGATATACCTAATG[C/T]TAAATGACGAGTTAA	84708
rs189719083	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53616375	TCTTCAGTGTCCTGC[A/G]CCTGGGTCAGCAGCA	84708
rs189772300	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53548722	ATAAAGACATATGCA[C/T]GCAAATGTTCTTTGC	84708
rs189807767	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53583204	ACACAGAGGATGGGC[A/T]GTGTTCTGTGGGCTA	84708
rs189809553	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53632782	AAAGAGGCCTCTATG[C/G]ACAACAGACAAGGAA	84708
rs189816156	snp	C/T	0.00676609	0.0577691	intron-variant	LNX1	GRCh38.p7	4:53564920	CAGGTCACTCCCACC[C/T]GAATACTGCGCTTTT	84708
rs189823612	snp	A/G	0.00279162	0.0372561	intron-variant	LNX1	GRCh38.p7	4:53467103	CCCCCCAGTAGGGGC[A/G]GACTGACACCTCACA	84708
rs189838081	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53622268	TGGCATTTGCAATAA[A/G]TCCAACTTTGTTCTG	84708
rs189840037	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53651396	GAACATAGTTTATCG[A/G]CATTTGTTGAAGTGA	84708
rs189844094	snp	C/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53602854	AAGCCAAATATACCT[C/G]AAAGCATAGAAATTT	84708
rs189848564	snp	A/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53586924	AATAATCCTATGAGA[A/T]CATTAAGGTAATCTT	84708
rs189860464	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53571252	CTCAAACTCCTGATC[C/T]CAAGTGATCTGCCTG	84708
rs189870639	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53551824	TTGGCCTCTCACCCT[A/G]CCTTATGACCCTTGG	84708
rs189881202	snp	A/G	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53646754	TCTATTCTCCAGTTG[A/G]AGCAACCACAGTTTC	84708
rs189891160	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53626964	TTACTCATCATACAC[A/C]TTTGACAAAATGTAT	84708
rs189892054	snp	C/T	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53483070	CCTTGAATTGTAGCT[C/T]CCATAATTCCCATAT	84708
rs189895226	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53608427	GATACCATCTCACAC[C/T]AGTCAGAATGGCTAT	84708
rs189899195	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53468947	GACACAGAAAGTTAA[C/G]AAGGATATCCAGGAA	84708
rs189905167	snp	A/G	0.00676609	0.0577691	intron-variant	LNX1	GRCh38.p7	4:53537514	ATAGCAATACACAGT[A/G]AGTAGTTTCAAAGGA	84708
rs189923801	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53504417	ATCAAAGAAAGTTAG[A/G]ACCTTCCTCTGGATT	84708
rs189934307	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53525801	CTTTCAGGGAGGGCA[C/T]TCTGAAGGCCAGGAA	84708
rs189935355	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53497254	CAGCCAGAGCCCCCT[A/G]TGTTGGAAGAAAACA	84708
rs189950925	snp	C/T	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53626086	TATTGACATATGTTG[C/T]GACATGGATGAACCT	84708
rs189954396	snp	A/C	0.0402882	0.136092	intron-variant	LNX1	GRCh38.p7	4:53467595	TTAAAAACCTTGAAA[A/C]AAAATTAGACAAATG	84708
rs189968871	snp	C/T	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53560649	CCTAATTCTTTCTGC[C/T]TGGAACTTGTACATA	84708
rs189989104	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53650079	ATAGATGAGCAGACC[A/G]AGTGGAATAGAATGA	84708
rs189993350	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53542565	CAAAATTTATGGATG[A/G]CACTGAGGTGGGGAA	84708
rs189997774	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53598008	TGAACTAACTACAAA[C/T]AGGTGAAGAGACTGA	84708
rs190005491	snp	G/T	0.00517822	0.0506191	intron-variant	LNX1	GRCh38.p7	4:53611628	AGGTTGGGGCAAAAG[G/T]AATTGTGGTTTTTAC	84708
rs190007679	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53578221	TAGAAAGCTTTAAAT[A/C]TCTTCAGGCTCTATT	84708
rs190008629	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53515543	AAATGACAAGAAGAC[C/T]GACTTAAGAAACTGA	84708
rs190014749	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53535602	CTCAGAGGTAAATGT[C/T]ACTATCAATTATAAA	84708
rs190126975	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53468560	GGCAAACTGGATAAA[C/G]TCAAGACCCATCAGT	84708
rs190162561	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53545357	CAGCCCCCCAACCTG[A/G]CCCTACTGAATTATA	84708
rs190169191	snp	C/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53465075	GCTATTCTTCCAAGC[C/G]TCTTGCATTTTGCCC	84708
rs190173320	snp	A/C	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53478467	GGCCGATCACTCCCA[A/C]ATTCTCTCATTAATT	84708
rs190181069	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53574854	GCTCAATAATTCTTA[C/T]ATGTATTTGTTACTG	84708
rs190193764	snp	G/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53646290	GAGTGGAGTAATAGG[G/T]CATGGTGGGGACTGT	84708
rs190221857	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53562933	AATAAAATTTGGGCC[C/T]GGCACAATGGCTCAA	84708
rs190232241	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53528134	TTGTGTCCGCTCAGC[A/G]TATTTTCCCTTTGAA	84708
rs190242576	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53640536	CACATACATTTCATT[A/G]CTAAAAATAAAGAAT	84708
rs190250730	snp	A/C	0.000798403	0.0199641	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53600345	TGGAGTGGGAAAGGC[A/C]AAAGCCAGAGGAGAA	84708
rs190261369	snp	C/G	0.00358779	0.0422022	intron-variant	LNX1	GRCh38.p7	4:53631200	TCTTCCCCACTACCT[C/G]GTGAGAGTGAAGGAT	84708
rs190346505	snp	A/G	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53627589	GAATCCTGTCAAATG[A/G]AAGAAAAGAAAATTC	84708
rs190354176	snp	C/T	0.00398564	0.0444627	intron-variant	LNX1	GRCh38.p7	4:53527365	GATGTAGAGCACTTT[C/T]ATAATGTGGTGTGAT	84708
rs190375207	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461232	AGCTTGTGTTAGAAG[A/G]AATGCTAAAAGTATG	84708
rs190382978	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53486158	CTTTCCCTCCCAAGA[A/G]CTGAAGCATTAGACT	84708
rs190387778	snp	C/T	0.00438332	0.0466095	intron-variant	LNX1	GRCh38.p7	4:53647786	CTTTCCCTCAGCCCC[C/T]GGCAACTGCCATTCA	84708
rs190420364	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53590457	AGCTGGGCTTAAAAA[C/T]GGTTTCCTTTCTCTG	84708
rs190449864	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53523237	TATGAAGAATGTTCT[A/G]TTTTGAATTGTGAAA	84708
rs190453628	snp	A/C	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53618705	CATACAGAGGTTTAA[A/C]TTTTCCAGTAGCCAC	84708
rs190459315	snp	A/G	0.00438332	0.0466095	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53598501	GCCTCCCAAAATGGT[A/G]GGACTAGAGGTGTGA	84708
rs190460008	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53581254	TTTAATGGCTAATTT[C/T]TTTCAGATCATTAAG	84708
rs190470948	snp	C/T	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53578571	TCGTTATGGGGTCCA[C/T]GACTGTAGATATGTC	84708
rs190479739	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53482167	GGTTGTACCACACAC[A/G]AGCCATGCCCTAAGT	84708
rs190480542	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53546041	CAAACTCCTGACCTC[A/T]AGTGATCCACCCACC	84708
rs190495189	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53620179	TTTTATCTATCTGTC[A/G]TCTGTCTATTTATCT	84708
rs190499937	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53638539	CTGGCTTCTTGTGTC[A/G]GCTTTCATACTATCA	84708
rs190501904	snp	C/G			intron-variant, missense	LNX1, LOC101928879	GRCh38.p7	4:53575393	CTTTGCATCTAGGAA[C/G]TCTCTTGCGTAGAAA	84708
rs190510184	snp	G/T	0.00597247	0.0543191	intron-variant	LNX1	GRCh38.p7	4:53555985	GGAATCTTTGTGTAG[G/T]AATAGCAGGAATCTG	84708
rs190512136	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53602080	TAGCCTTATGGTTCT[A/G]CTGGTGTGATAGAAA	84708
rs190518091	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53582410	AAGATCACAAAACGA[C/G]CGGATCCTGTAAGAG	84708
rs190530698	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53540014	CCAGTTGTTTTTGCT[C/T]GGGCTACTAATCAAT	84708
rs190541251	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53551387	CAGTTTCCCAATAAA[C/T]AGAAAACACCTGAAA	84708
rs190543683	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53621804	ACATGAAATGGGCAC[C/T]GATTTGAGAGTTGGA	84708
rs190547307	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53641735	CTTTCTATAACTAGA[C/T]TGCTTGCACATTCCA	84708
rs190565943	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53514124	ACCTGATTTAAACAG[C/T]GGCTTCTTTTCTGGC	84708
rs190575377	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53534705	AAACAACCTATTTGT[C/T]TTTGGGGGAGGATGT	84708
rs190663297	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53501549	TTTGGCCTCCAAGTG[C/T]TAGGATTACCGGTGT	84708
rs190667345	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53521373	CCGTTCCTCAAAGTG[C/T]ATTCCATCGCATTCT	84708
rs190689030	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53503683	TTTTGAAATGATAAA[G/T]GAGCACTGGACCCCA	84708
rs190694684	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53465287	ATGGTTCAAACATTT[G/T]TGACAGAACTTCTCT	84708
rs190723000	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53555221	TTCCTGCTCCCAAGC[A/G]TGCTAAACTGGCCCA	84708
rs190725515	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53521063	TGGGCTATGGATCAA[C/T]GGTGCTTTCTATTTC	84708
rs190728468	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53466719	TCGGAGGGTCCTATG[C/T]CCAAGGAGCCTTGCT	84708
rs190751922	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53592554	AAACTGTGGATTCCC[C/G]GTCCCGGAAGATGGC	84708
rs190843258	snp	A/G	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53470205	TGCAAATCAATAAAC[A/G]TAATCCAGCATATAA	84708
rs190849481	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53491240	ACATGAAAAAGTACT[G/T]GTGGTCACCTAAAAG	84708
rs190850649	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53619231	TAAAACGTACACTTT[A/G]GTGGTTTTTAGTTTA	84708
rs190855446	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53539265	AGGCCAGGGTCTGGA[C/T]CTTCTCACTATAAAA	84708
rs190908412	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53509660	CAAATTCATTAAAGT[C/T]GTCATGGTATCTACA	84708
rs190920495	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53529746	AACTTATTACACAGT[A/G]CAGGTAAGGCTGGGC	84708
rs190933735	snp	A/G	0.00716266	0.059414	intron-variant	LNX1	GRCh38.p7	4:53539789	TCAAAGATATTGCTC[A/G]CTTCATATTTTCAAA	84708
rs190966649	snp	C/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53575235	GATCCACCTGCTTTG[C/G]CCTCCCAAAGTGCTG	84708
rs190967131	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53474366	AAATTTTATTGGAAC[A/G]CAGCCTTCCTCATTC	84708
rs190967648	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53500600	ATTAAAATTATTTCT[A/G]AGTATGTTAGGGCAA	84708
rs190996604	snp	G/T	0.00279162	0.0372561	intron-variant	LNX1	GRCh38.p7	4:53613104	AGATTATTAATATGG[G/T]CTTTCTGGGTAAGTG	84708
rs191006095	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53643571	TGATATAGACACAGA[C/G]ATAGGGTAACAAAAT	84708
rs191016072	snp	A/G	0.000798403	0.0199641	utr-variant-5-prime	LNX1	GRCh38.p7	4:53652329	GCTCCACCTTTGTAC[A/G]TGCGGGGGTTAACCT	84708
rs191055409	snp	A/C	0.00159617	0.0282053	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53598990	TAGAAATTGCTTAAC[A/C]GAGGAGTGTTACAGA	84708
rs191059913	snp	C/T	0.00358779	0.0422022	intron-variant	LNX1	GRCh38.p7	4:53494997	AAGGGTTAAGGAGGA[C/T]GTGGGGCGGGGAGGG	84708
rs191064053	snp	A/C	0.0107246	0.0724382	intron-variant	LNX1	GRCh38.p7	4:53571806	ACTAAGACTGCAGGC[A/C]GACATCACCAGGTCT	84708
rs191077033	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53536262	ATCCCATGGGAAATA[C/T]CTAACAATTTCTTCC	84708
rs191090255	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53473620	GAACTCATGGACACA[A/G]TGAGGGTGACAACAG	84708
rs191099079	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53639378	AAAAACTATTGGGTG[C/T]TATGCTCAGTACCTG	84708
rs191108367	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53493652	TGTTTAGATAACCAA[A/G]TCCTTGAAAGCAAAC	84708
rs191131601	snp	A/G	0.00795532	0.062565	intron-variant	LNX1	GRCh38.p7	4:53645209	AATTAAGAATCCAGA[A/G]GAAGGGCTCCTTTGG	84708
rs191179744	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53494395	GTCTTTATCAGCAGC[A/G]AGAGAATGGACTAAC	84708
rs191247849	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53474852	GCTCACTGCAACCTC[C/T]GCCTCCTGGGTTCAA	84708
rs191299131	snp	A/G	0.00517822	0.0506191	intron-variant	LNX1	GRCh38.p7	4:53608879	AACCAAATACCACAC[A/G]TTCTCACTTATAAGT	84708
rs191301024	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53638020	GATAGATGGCAGCCA[C/T]GATGGTGGCATTTTA	84708
rs191304593	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53587585	TTAGAGCATCTCTTA[C/T]GTGTCCTCGCCTTGC	84708
rs191311917	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53516263	TTAAAAAAAGAATCA[C/T]GCAAAATGCCAAACA	84708
rs191312573	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53553473	CTTCTGATATGGGTG[G/T]TCCTCAGAACCTACA	84708
rs191317967	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53552567	GGCGCAGTGGCTCAC[A/G]CCTGTAATTCCAGCA	84708
rs191329163	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53465963	ATAGTATATTGGCAT[C/G]TACTTCCAGTGACTT	84708
rs191335609	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53510298	TATTTAACTGATGGC[A/T]CATTTTAAAATGTCA	84708
rs191341236	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53610414	AAACTATATATGAAA[A/C]ATTTTGTAGTTAAAA	84708
rs191343032	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53589169	ACTGGACATTTCCCC[C/T]GAAAGGCCCATGGAG	84708
rs191343606	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53480956	TGAAAGAAGCTCATC[A/G]GCATCACAACAGGAT	84708
rs191345484	snp	A/C	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53531298	AAACTGGGTCAGAAA[A/C]GAAAAGGCCACCTGT	84708
rs191347614	snp	A/C	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53503022	TGCAAGCTCCGCCTC[A/C]CAGGTTCACATCATT	84708
rs191353233	snp	A/G	0.000399281	0.0141238	missense, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573747	TGGACTTCTTGCAGT[A/G]CTGCAGAACCAGAGG	84708
rs191372211	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53629832	TTTTATTTTTAAAAA[A/T]TATTGCAGGTACGCC	84708
rs191374800	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53648594	TCCTTTGGTGCCCAG[A/G]CATTTTTTATTTTGA	84708
rs191455703	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53505201	AGGCCGGTGCCTTAC[A/G]TATAATAATCTGTTT	84708
rs191461109	snp	A/C	0.00279162	0.0372561	intron-variant	LNX1	GRCh38.p7	4:53526926	ATAGAGCTAATTCTT[A/C]TTTGTAAGAGACACA	84708
rs191485797	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53526675	ACAATACCCTATTCC[A/G]TCTTTCTGCCTTCAC	84708
rs191508283	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53561114	GGTTCAGAGTTAGAA[A/G]GTCACAGTAAGGATG	84708
rs191512114	snp	A/G/T			intron-variant	LNX1	GRCh38.p7	4:53586287	GCCTAAACATGCTGC[A/G/T]CTCTATTCAGAAAAG	84708
rs191514022	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53484568	ACTCCATCTCAAAAA[A/C]AGAAAAAAAAAATCT	84708
rs191585206	snp	C/T	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53468213	AAAGAAAAGAATTTT[C/T]AACCCAGAATTTCAT	84708
rs191587224	snp	A/C	0.00636936	0.0560724	intron-variant	LNX1	GRCh38.p7	4:53484856	TTCTGAAAAGGGCCC[A/C]AAAAAGAAGTTGGAG	84708
rs191615199	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53613704	TTCTTTATCCAGTCT[A/G]TGATTGATGGGTATT	84708
rs191657623	snp	C/T	0.00755907	0.0610114	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53506905	GCTACCTCATAGGGT[C/T]GTTGTGAGGCTTAAA	84708
rs191660645	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53651738	ATGCAACACCTACTC[C/T]TACTGTGGAATGAAA	84708
rs191674429	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53544951	GCACTCGACCAGCAC[A/G]TCCCCAGTGACACCT	84708
rs191690389	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53485872	TTTCACACCTATGTG[A/G]TATGTACCAAGAAAG	84708
rs191748415	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53543060	AGATGAGGGTCTCAC[C/T]ATGTTGCTCAGGCTT	84708
rs191761685	snp	A/G	0.0103295	0.0711199	intron-variant	LNX1	GRCh38.p7	4:53469310	GAACAAAGACACAGC[A/G]TACCAGAATCTCTGG	84708
rs191766155	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53467885	GTACCTGAAAGTGAC[A/G]AGGAGAATGGAACCA	84708
rs191768809	snp	C/G/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53606862	GACAAAAACCCACAT[C/G/T]ATTATCTCAATAGGT	84708
rs191772267	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53547484	GTCAGTCTGACTGCA[C/G]AGCATGTGCCTTGAA	84708
rs191784094	snp	G/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53504741	AAAGGCTATTGTAGG[G/T]TTACTAATTGGCTTA	84708
rs191784165	snp	C/T	0.0267878	0.112589	intron-variant	LNX1	GRCh38.p7	4:53570625	CGTATGTAACTAACC[C/T]GCGTAATGTGCACAT	84708
rs191786133	snp	A/G	0.00159617	0.0282053	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53509033	AAAAAGAACATTCTC[A/G]AGGCTCAGAAGACCA	84708
rs191786192	snp	A/G			intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53499411	TGATCCACCCACCTC[A/G]GCCTCCCAAAGTGCT	84708
rs191818874	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53464087	GAAAGACGACAGTGG[A/G]TGTAGGATGTTTTGA	84708
rs191842206	snp	C/G	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53649759	GGTGCCCTCCGATGG[C/G]AGGCTGTGTAGGGTC	84708
rs191858112	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53602408	ACTGTACCTGGGCCA[A/G]CATCAGCTGTCAGAG	84708
rs191864743	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53599532	GCCGTTCTTTTATTC[C/G]TCTACTTTCTTAATA	84708
rs191871898	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53580011	TTTATAGTCACATGG[C/T]GGTGTGTCCTGCATT	84708
rs191875528	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53564330	ACAGCCACCTGCTAG[A/C]CCTTCCCCTTCCCCA	84708
rs191878526	snp	C/T	0.00318978	0.0398085	intron-variant	LNX1	GRCh38.p7	4:53562134	GATGAGATTACAAAA[C/T]GGAAATGTGGTCTTG	84708
rs191892327	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53619782	AATTTTTCGATGAAC[G/T]GTCAAACTGTTTTTC	84708
rs191908281	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53633299	ACCACCCCCATCCAC[A/G]CATGGTTCTGCACTA	84708
rs191916317	snp	C/G	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53593382	GGGTGGGCAGGGGAA[C/G]GGTGTAGGTGAAATG	84708
rs191964297	snp	C/T	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53640298	GCAGACCAGGGAGCC[C/T]ACAAGGAGACAATGA	84708
rs191979731	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53599966	TGTGCTCAGCAGGTG[A/G]CAGTAACATCTGTAG	84708
rs191990027	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53475574	GTACTAAAACTAAAC[A/G]TCTCACTTTCATTTT	84708
rs191995071	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53495835	AGGCATGGGCCACCA[C/T]GCCCAGCCGAGTAAT	84708
rs192009642	snp	A/C	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53516894	AAGGAATGAAGTTGA[A/C]AACAGAGGGCTCGCA	84708
rs192040199	snp	A/G	0.00318978	0.0398085	utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460676	GAAAAAATATAAACA[A/G]TGTTGTAGAGTAATG	84708
rs192041348	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53529202	TAGGCACTGAACTGA[C/T]ACAATCTAGGAGATA	84708
rs192046881	snp	C/T	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53573077	TCAGAGAAATCTGCT[C/T]ATACACCCTCTCTGG	84708
rs192048766	snp	C/T	0.00358779	0.0422022	intron-variant	LNX1	GRCh38.p7	4:53642724	AAATCAGCAAGCCTG[C/T]GGGGTCTGAGGTTTC	84708
rs192057894	snp	A/G	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53553208	GGGGACACAGAGAGG[A/G]GTGATAATTTTCAAC	84708
rs192064197	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53563612	TGATCTCAGCTCACT[A/G]CAACCTCTGCCTCCC	84708
rs192071864	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53536623	GTGCTTCCATTTCCA[C/T]ATTGCTTCTTCATAA	84708
rs192079349	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53489977	TGTTTACAGTACCAC[A/C]AAAGTTCTACCCTTT	84708
rs192135515	snp	C/T	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53478283	AACTACATTATGCCA[C/T]TTAATAGAGGTAACT	84708
rs192139949	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53547928	CTGACAGGGACCTAC[A/C]AGTTGTGAATTCACA	84708
rs192157125	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53635099	TCTTCCAAAGTGCTG[A/G]AATAGCACGCATGAG	84708
rs192163920	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53522948	TATGATTTTTGTATT[C/G]ATTCTGCTATCAATT	84708
rs192174069	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53541381	AAAGTGTGAACAATT[A/G]GTGCCAAACTATTCA	84708
rs192176396	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53582569	TGAATTTTTGCACAT[C/T]TAAAAGTTATTCAAA	84708
rs192207322	snp	A/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53595223	TCATAGCAGATATCT[A/G]TTGGGGAGGAACATG	84708
rs192215690	snp	A/T	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53623689	ATGTTTTATTTTTGT[A/T]AAAACCACCGAGAAT	84708
rs192215830	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53644073	TAGACTGCACTTACT[A/G]TGTTTTGTACTTCAT	84708
rs192224003	snp	C/T	0.000399281	0.0141238	intron-variant, missense	LNX1, LOC101928879	GRCh38.p7	4:53576220	ACCAGTGCCCTGGCT[C/T]GCTTCCTGCAGCCGA	84708
rs192231017	snp	A/G	0.00557542	0.0525036	intron-variant, utr-variant-5-prime	LNX1	GRCh38.p7	4:53558263	ACCAGCCCCTCCTGC[A/G]GGATGCGGACTGGTT	84708
rs192233709	snp	C/G	0.00358779	0.0422022	nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53604399	AAGGGAATGTTTGGA[C/G]AAAAGTGATGAATTC	84708
rs192263922	snp	C/T	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53491542	AAGTTGCTCAGTCAA[C/T]AATCACTGAACAAAT	84708
rs192267921	snp	C/T	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53557128	CTGGAAAAATATCAC[C/T]AGAGGTTGGTGACAT	84708
rs192299598	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53522324	CTTCATAGTGATCTC[C/T]CCCCTCTCAATGCAT	84708
rs192301336	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53594661	AGTTGGTTTTACCCC[C/G]CAAGATCAAACCCTT	84708
rs192359191	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53492765	CATTTTTATAGACTA[C/G]GAATGGCCTAGGGGA	84708
rs192359847	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53476460	CCTCTGCCTGTCTGT[A/G]GAGCTCTCTGCTGCA	84708
rs192360209	snp	A/G	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53579098	CAAAAGTAAGAGAGA[A/G]GGCCTGTCAGCTTTG	84708
rs192364891	snp	A/G	0.00478085	0.0486577	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53511296	GGTGACTAATACTGG[A/G]GCAGCTTGATTTACA	84708
rs192369595	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53518244	AAGCAAGCACACTGA[C/T]TTGGTTTACCAAAGA	84708
rs192377722	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53556723	AATCCTGAAATGCAG[A/G]ACAAATGATCACTTC	84708
rs192393124	snp	G/T	0.00953873	0.0683987	intron-variant	LNX1	GRCh38.p7	4:53471089	TACCTGACTTCAAAC[G/T]ATACTACAAGGCTAC	84708
rs192425032	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53621897	TTTGTTGCCTCATTA[A/G]TAAGTGAAGAAGTTG	84708
rs192537149	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53615838	GATACAGGCATGCAA[C/T]GCGTAATAATCTTAT	84708
rs192604216	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53468389	GCTACTGCAAAAACA[C/T]GCCAAATTGTAAAGA	84708
rs192605758	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53615312	GCTTCTCCCAACAGG[A/G]GGCAGGGAGTATTTC	84708
rs192621130	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53550361	CCCATTTCCTCTGTA[A/G]ACTCTACCTCCTTCC	84708
rs192622612	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53593790	GCTACTTATTGTTCT[C/G]AGCACTTTATACAAG	84708
rs192631074	snp	C/T	0.00358779	0.0422022	intron-variant, synonymous-codon	LNX1, LOC101928879	GRCh38.p7	4:53575613	ATCCCACCTTGGGAC[C/T]AGGCCCGCTTTTGGC	84708
rs192631530	snp	G/T	0.00755907	0.0610114	intron-variant	LNX1	GRCh38.p7	4:53532983	GGGGAGCCCATATAT[G/T]GTTTTCCTGGGGTTA	84708
rs192642898	snp	A/C	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53633780	AGAGCTGATTGCCAC[A/C]GTCAGGCACTAAGAT	84708
rs192708962	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53541268	ATACCATTAGCAACT[A/G]AATCAACTTCAGCAA	84708
rs192710259	snp	A/G	0.00159617	0.0282053	intron-variant, missense	LNX1, LOC101928879	GRCh38.p7	4:53576083	CCCAAGACCTGGTCG[A/G]GGACTTGGCCAGCGT	84708
rs192717781	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53537217	TGCACGAACATCTGA[C/T]GCTTCTCATGGAGTC	84708
rs192737620	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53496809	TCAAGCCGAGTTGAC[A/G]TTTTCTTCCCAAAAA	84708
rs192740665	snp	C/T	0.00835141	0.0640778	intron-variant	LNX1	GRCh38.p7	4:53561485	CCCACGTCATCCTCC[C/T]AAAGTGCTGGGATTA	84708
rs192767930	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53640038	TGAGACTCTGTCTCA[A/G]AAAAAAATAAAAATA	84708
rs192768838	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53611107	CTAGAAAACCCAAAG[G/T]AATCTAATAAAAGTC	84708
rs192777885	snp	C/G	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53574649	TTCACTCAGTTGGTC[C/G]TTAGTGGCTAAGTGG	84708
rs192798205	snp	C/G	0.000103939	0.00720825	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461621	GTAATCAGTGTACAT[C/G]CATATTTAAGTTTCA	84708
rs192888711	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53467923	AAACACTCTGCAAGA[C/T]AATATCCAGGAGAAC	84708
rs192892238	snp	A/C	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53486711	AAAAGAGGGTTAAAA[A/C]TAAGTAGCGTCTGTA	84708
rs192895364	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53628828	ATGTCTTTTACAATG[A/G]CTTGGACGAAGCAGG	84708
rs192896620	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53562651	TAAGTCTCCTGTTGG[A/G]CAACAGGTGCAGAAA	84708
rs192898804	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53527536	CTCCTTGGCTCCACT[A/G]GTTCTGGAGGGCAGG	84708
rs192903046	snp	A/G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53588678	GTACACCATTTTAGC[A/G/T]TCCTTTGGGGAAAAA	84708
rs192918549	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53584008	ATTTTTGCATTGATT[C/T]GGAGCTCTGTTCATG	84708
rs192920543	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53510877	TGGGAGGACACAGCA[C/T]GTCCTAGTAAAAGAA	84708
rs192925753	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53549449	GAATGAAGAACGGAG[A/C]AGAGGAGGAGGAGGT	84708
rs192952341	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53616380	AGTGTCCTGCGCCTG[C/G]GTCAGCAGCACATGA	84708
rs192989908	snp	A/G	0.0185938	0.0946107	intron-variant	LNX1	GRCh38.p7	4:53470955	CATCCCCATCGAGCT[A/G]CCAATGACTTTCTTC	84708
rs192999052	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53631038	GAACCTTGCAGTAAG[A/T]GCTCCTGGGCCAAAA	84708
rs193018260	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53648116	TTCTTTTGGGTATAT[A/G]CCAAGAAATTGAATT	84708
rs193032425	snp	C/T	0.0197687	0.0974348	intron-variant	LNX1	GRCh38.p7	4:53540625	AGGGGGAGGTTGCAG[C/T]GAGCCGAGATTGCGC	84708
rs193042659	snp	A/G	0.00279162	0.0372561	intron-variant	LNX1	GRCh38.p7	4:53465570	AATGCAACTGCACCA[A/G]CATAACATACCCCTA	84708
rs193066253	snp	A/C	0.00676609	0.0577691	intron-variant	LNX1	GRCh38.p7	4:53468601	CAGGAAACCCATCTC[A/C]AGTGCAGAGACACAC	84708
rs193126931	snp	A/G	0.00755907	0.0610114	intron-variant	LNX1	GRCh38.p7	4:53568171	TTCATTCTGATACCA[A/G]AGCCGGGCAGAGACA	84708
rs193128556	snp	A/C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53581152	AGGAGGTATACTGGT[A/C/T]ACCCGGGACCATGAC	84708
rs193132847	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53609187	GTTTATTACCTGGCT[A/G]GAAAAATCATCTGTA	84708
rs193136631	snp	C/T	0.000399281	0.0141238	nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53605370	TTATTAAAGTGATTA[C/T]TAGTCAAGCAAATTA	84708
rs193141781	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53644614	GACTCTCATAGCAAA[C/T]ACCTGGGAACTCATA	84708
rs193146415	snp	A/G	0.00159617	0.0282053	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507568	TAAGACATTAACAGT[A/G]ACTACCTCTGGGTGG	84708
rs193154105	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53545626	TATAGTGCACTTAAA[A/G]TGTTCCAGGCATCTA	84708
rs193160893	snp	A/C	0.00597247	0.0543191	intron-variant	LNX1	GRCh38.p7	4:53491976	ATTTTTAGTAGAGAT[A/C]GGATTTCACCCTGTT	84708
rs193163479	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53566410	ACTAAGCTTCAGAAG[C/T]GAAGGAGAAAGAAAA	84708
rs193166422	snp	A/C	0.00478085	0.0486577	intron-variant	LNX1	GRCh38.p7	4:53532357	GGCACGCACTGTAGC[A/C]CCGGCTACTCGGGAG	84708
rs193174639	snp	A/G	0.00318978	0.0398085	intron-variant	LNX1	GRCh38.p7	4:53635906	TATTTCAAGCTGTAA[A/G]TATTTACTAAGTGTG	84708
rs193216574	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53522212	TCTACCACAGGTCTT[C/T]GTCCAATCTGGCTTC	84708
rs193225437	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53480187	ATGTCTCAGTTTTTT[A/T]AAATATGTTACTTTT	84708
rs193284535	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53624190	CTCTTTTATACCTTT[C/T]CAATCATTAGCCTAT	84708
rs193289347	snp	A/G	0.00279162	0.0372561	intron-variant	LNX1	GRCh38.p7	4:53584436	ATAATACATGGCAAT[A/G]TGTATAATGCCCCAA	84708
rs199501887	snp	C/G	1.71499e-05	0.00292825	missense	LNX1	GRCh38.p7	4:53496023	TGACCTCTGACTCAC[C/G]TGAATCAGATGAGCC	84708
rs199520931	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53646584	CAAATATAGGACCAA[C/T]ATGGCCAGAGTTTCC	84708
rs199525597	in-del	-/C			intron-variant	LNX1	GRCh38.p7	4:53543916	AAACAAACAAAAAAA[-/C]AAAACAATAAAAACA	84708
rs199531206	in-del	-/G			intron-variant	LNX1	GRCh38.p7	4:53466156	AACTTTTTGTTTTAA[-/G]AAAAAAAAAATCACA	84708
rs199532279	in-del	-/GA			intron-variant	LNX1	GRCh38.p7	4:53618286	GGACTTGAGCCTTGG[-/GA]GAAAAGAGTATTCTA	84708
rs199543447	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53565815	TAAAGGAGCTGATGG[A/G]GCTGAAAACCAAGGC	84708
rs199546074	snp	A/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53596019	AACATTATGATTTGG[A/T]CTTGCTTATTACATT	84708
rs199547299	snp	G/T	0.150333	0.229274	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53501309	TTTTTTGGGGGTGGG[G/T]GGACAGGATCTCACT	84708
rs199552515	snp	A/C/G	0.000378913	0.0137593	missense, synonymous-codon, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498727	TAATGATATGGACCA[A/C/G]TGGGGTTTCGCTACC	84708
rs199574435	snp	G/T	6.61485e-05	0.00575064	missense	LNX1	GRCh38.p7	4:53478741	ATTGTAGGATGGAGG[G/T]GCTGAAGGCACAGAT	84708
rs199598971	in-del	-/C			intron-variant	LNX1	GRCh38.p7	4:53544204	TCTCTCTCTCTCTCT[-/C]TTTTTTTTTTGAGAC	84708
rs199607707	snp	A/G	0.00199792	0.0315431	synonymous-codon	LNX1	GRCh38.p7	4:53496218	CTCGGGGCTACTTTT[A/G]TTGAGAATCACATGA	84708
rs199638031	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53570664	AAACTTAAAGTATAA[A/T]AATAAATAAATAAAT	84708
rs199652288	in-del	-/G			intron-variant	LNX1	GRCh38.p7	4:53618288	ACTTGAGCCTTGGGA[-/G]AAAGAGTATTCTAAA	84708
rs199669260	snp	C/T	0.000399281	0.0141238	intron-variant, missense	LNX1, LOC101928879	GRCh38.p7	4:53576313	AAGTTCCAGGAGCTG[C/T]GGTACAGCGTGGCCC	84708
rs199684449	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53590516	ATTGGGCTGTCAAGA[A/T]ACAGGCTGTGTGATC	84708
rs199684639	in-del	-/T			intron-variant	LNX1	GRCh38.p7	4:53495549	GCTTTTTTTTTTTTT[-/T]AAGATGGGTCTTGCT	84708
rs199688504	snp	C/T	0.000399281	0.0141238	synonymous-codon, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507432	ATTTATTTTTTTAAA[C/T]GATCTGCTTCTAATA	84708
rs199689159	snp	C/G/T			intron-variant	LNX1	GRCh38.p7	4:53568396	GCCAAAGACAAAAAC[C/G/T]ACATGATTATCTCAA	84708
rs199695427	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53614984	GAAATTTGTTCATCT[A/C]TGAACACCGAGAATG	84708
rs199698757	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53505800	ACACCTAAAAAGGGG[A/G]CTGAGGGAGTGAGGT	84708
rs199728272	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53583963	AACAACAACAACAAC[A/G]ACAACAACAACGACA	84708
rs199747919	snp	C/G	0.000378977	0.0137603	missense, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573966	CACACACTGCACACA[C/G]GGGTTCAGGATCGTT	84708
rs199766830	snp	C/T	0.305685	0.24372	intron-variant	LNX1	GRCh38.p7	4:53567868	GAATACTACAAACAC[C/T]TCTATGCAAATAAAC	84708
rs199788423	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53615389	TTCCAGAGCCTAGGT[A/G]TTCAAGAGGCTTCGC	84708
rs199817409	snp	A/G	4.94572e-05	0.00497254	missense	LNX1	GRCh38.p7	4:53476754	GTGTTTGGACTTACC[A/G]TGGTAATTCCAGCCA	84708
rs199823248	snp	A/G	0.000182091	0.00954003	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507467	ATCTCTCAAAGGGCC[A/G]TGCTGAGGAATAGCG	84708
rs199824448	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53568448	ATAAAATTCAACAAC[A/C]TTTCATGCTAAAAAC	84708
rs199833713	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53561711	CCCAGCCAGCCTTCA[A/G]CCACGTATGTCTTGG	84708
rs199867862	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53473770	CATGAGTTTACCTAT[A/G]TAACAAACCTGCACA	84708
rs199872849	in-del	-/T			intron-variant	LNX1	GRCh38.p7	4:53466167	TTAAGAAAAAAAAAA[-/T]CACATATTATTTGGA	84708
rs199877213	in-del	-/TC			intron-variant	LNX1	GRCh38.p7	4:53544189	TGAGAGGTGCTGATT[-/TC]TCTCTCTCTCTCTCT	84708
rs199893471	in-del	-/CAACAA			intron-variant	LNX1	GRCh38.p7	4:53472664	GAACAATGATTTATT[-/CAACAA]CAACAACAACAACAA	84708
rs199901616	snp	C/G	3.66764e-05	0.00428215	missense, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573810	CCAGGAAGTTGGTGA[C/G]GCAGAGGGTGCAGTA	84708
rs199911645	in-del	-/C	0.0197687	0.0974348	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53521671	TCTATAAAACATATT[-/C]CCAAAAATTGTGTTA	84708
rs199941942	in-del	-/AG			intron-variant	LNX1	GRCh38.p7	4:53644389	GCAACAGAGTGAGAG[-/AG]TCTATCTCAAAACAA	84708
rs199942853	in-del	-/G			intron-variant	LNX1	GRCh38.p7	4:53618292	TGAGCCTTGGGAAAA[-/G]AGTATTCTAAAGAGG	84708
rs199956752	snp	A/G	0.00199802	0.0315439	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507474	AAAGGGCCGTGCTGA[A/G]GAATAGCGACAGGAG	84708
rs199972385	snp	A/T			intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53574983	CCATTAGATATTTCG[A/T]TTTTTTTTTTTCTTT	84708
rs199980906	in-del	-/GAA	0.0174175	0.0916809	intron-variant	LNX1	GRCh38.p7	4:53468638	TCAAATAAAGGGATG[-/GAA]GAAGATCTACCAAGC	84708
rs199987263	in-del	-/TG			intron-variant	LNX1	GRCh38.p7	4:53642203	CTCCAGCCTGGGCAA[-/TG]CAGAGCAAAATCCTA	84708
rs200005530	in-del	-/AC			intron-variant	LNX1	GRCh38.p7	4:53472686	ACAACAACAACAACA[-/AC]AAAAAAAAAAAAACA	84708
rs200008404	snp	G/T			intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461960	CTTATGGATGTCATA[G/T]TTTTATTTACTTGAT	84708
rs200018589	in-del	-/C			intron-variant	LNX1	GRCh38.p7	4:53543908	AAAAACAAAAACAAA[-/C]AAAAAAACAAAACAA	84708
rs200020412	snp	A/G	0.00199792	0.0315431	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507322	GTTCATTTACCTTCA[A/G]GGGCAGTGGTGTTTT	84708
rs200028759	snp	A/C			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53515520	AGGCCCCCACCCCAC[A/C]AAAAAAAAAATGACA	84708
rs200029268	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53549476	AGGTTGAAAGAAACT[A/T]AAGAGATGTGGCAAC	84708
rs200040467	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53474823	CCAGGCTGGAGTGCA[G/T]TGGCGCGATCTCAGC	84708
rs200081802	snp	C/T	1.64735e-05	0.00286993	synonymous-codon	LNX1	GRCh38.p7	4:53496185	CACCTTGCGCACCAG[C/T]TTTATTCCAAGCTGC	84708
rs200094733	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53652018	AATTTGATGTGTGTG[A/T]GTGAGAGAGAGAGAG	84708
rs200119516	snp	A/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53512379	TAATCTCTGGTAATT[A/T]AAAAAAACTGCCAAC	84708
rs200142116	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53479641	AGAGATGACTTTTCT[A/T]TCTATCTTTTTTCGC	84708
rs200173285	snp	C/T	3.33106e-05	0.00408095	intron-variant, utr-variant-5-prime	LNX1	GRCh38.p7	4:53557977	TCATTCTCCGAGCAG[C/T]GTGCTGCCTTCTCCC	84708
rs200182710	snp	C/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53603534	TGCTTCATGATTCTG[C/T]AGGCTGTAAAGGATG	84708
rs200184950	snp	C/T	0.000516533	0.0160624	missense	LNX1	GRCh38.p7	4:53496348	GGCTGCCGCAGGAGA[C/T]GCACAGCGTAGTTGT	84708
rs200186848	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53552499	ACTAGCACCACTCCA[C/T]CAAATTCTAAGTTTT	84708
rs200191377	snp	G/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53501298	TTTTTTTTTTTTTTT[G/T]TGGGGGTGGGGGGAC	84708
rs200206377	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53570607	CAGCATGGCACATGT[A/G]TACGTATGTAACTAA	84708
rs200216018	in-del	-/A			intron-variant	LNX1	GRCh38.p7	4:53495279	ATAAAAAAGCTAAAG[-/A]AAAAAAAAATTTCAA	84708
rs200237039	snp	A/G	1.64895e-05	0.00287132	missense, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498826	CATCTGGAATCAGGT[A/G]GTACAACCTTGGAAA	84708
rs200260602	snp	C/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53501304	TTTTTTTTTTTGGGG[C/G]TGGGGGGACAGGATC	84708
rs200324062	snp	A/G	0.00199792	0.0315431	synonymous-codon, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508197	CCTCTTCCTATCTTT[A/G]GTCAGGCCGTAGTGG	84708
rs200331237	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53523319	GTATCACTCTGAAGA[C/T]AAGGTCACCCAGGCT	84708
rs200339068	snp	C/G/T	0.000513419	0.0160139	synonymous-codon	LNX1	GRCh38.p7	4:53478566	CCTTTACTTTTTACC[C/G/T]GTTTTTATTCTTCCA	84708
rs200343239	in-del	-/A			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53501285	TGATAATAATCTTTT[-/A]TTTTTTTTTTTTTTG	84708
rs200360982	in-del	-/CACA/CACACACACACACACACA	0	0	intron-variant	LNX1	GRCh38.p7	4:53529135	ACACACACACACACA[-/CACA/CACACACACACACACACA]AACACATGCACACAC	84708
rs200384757	snp	A/C/G	9.97888e-05	0.00706289	missense	LNX1	GRCh38.p7	4:53481781	TTGCTGTTCCAGCCG[A/C/G]CTTCCTGAAAGATGT	84708
rs200392918	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53516159	AGGCAGGAGGACTGC[C/T]TGAGCCCAGAAGTTC	84708
rs200405268	in-del	-/AACAACAACAAC			intron-variant	LNX1	GRCh38.p7	4:53583933	AACTGACCCCCTGCA[-/AACAACAACAAC]AACAACAACAACAAC	84708
rs200410776	snp	G/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53517974	CAACCACACACGGCT[G/T]CCCCTCATTAGCCCC	84708
rs200448899	in-del	-/AG	0.020168	0.098373	intron-variant	LNX1	GRCh38.p7	4:53647487	ACCAATTTCTAACCA[-/AG]AGATATTTTTCTGTA	84708
rs200473786	in-del	-/CGGCC			intron-variant	LNX1	GRCh38.p7	4:53613984	TCTGTTATTTTTTGA[-/CGGCC]CTTTTTTGATAATAG	84708
rs200529974	in-del	-/TAAA			intron-variant	LNX1	GRCh38.p7	4:53570698	AAATAAATAAATAAA[-/TAAA]AGAAAAATATTTACA	84708
rs200552235	snp	C/T	0.305685	0.24372	intron-variant	LNX1	GRCh38.p7	4:53568293	CATCAAAAAGCTTAT[C/T]CACCATGATCAAGTG	84708
rs200583618	snp	A/C/T	3.30196e-05	0.00406309	intron-variant, synonymous-codon	LNX1	GRCh38.p7	4:53557957	GACCAGCAACAGAAG[A/C/T]GCCTTCATTCTCCGA	84708
rs200593333	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53554006	GGTCATTCCTTATCT[A/G]TGAGAAACAGCTTAG	84708
rs200607142	in-del	-/A			intron-variant	LNX1	GRCh38.p7	4:53540216	CAAAACCCTGTCTCT[-/A]AAAAAAAAATACAAA	84708
rs200612730	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53623206	GCGTTGAGAGCAATT[C/T]TTTTTTTTTTTTTTT	84708
rs200622106	snp	G/T			intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53574460	ACAAGAAAAAAAAAA[G/T]AAAAAACAGTTAACA	84708
rs200623322	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53590517	TTGGGCTGTCAAGAT[A/C]CAGGCTGTGTGATCA	84708
rs200623888	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53568399	AAAGACAAAAACCAC[A/G]TGATTATCTCAATAG	84708
rs200629009	snp	A/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53502949	CTTTTTTTTTTTTTT[A/T]AGATGGAATCTTGCT	84708
rs200643292	snp	A/C/T	0.00399205	0.0444982	intron-variant	LNX1	GRCh38.p7	4:53496435	GGTCAGCTCCACCTG[A/C/T]CACAACCCTTCCTGA	84708
rs200711838	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53466157	ACTTTTTGTTTTAAG[A/G]AAAAAAAAATCACAT	84708
rs200713622	in-del	-/A	0.0158469	0.0875917	intron-variant	LNX1	GRCh38.p7	4:53587662	CAAGAGAGTGAAAGG[-/A]AAAAAAAAAGTAGTC	84708
rs200751020	in-del	-/AGG			intron-variant	LNX1	GRCh38.p7	4:53539390	TAATTTTTGAGACCT[-/AGG]GTCTCACTCTGTCGC	84708
rs200764921	in-del	-/ATC			intron-variant	LNX1	GRCh38.p7	4:53479645	ATGACTTTTCTATCT[-/ATC]TTTTTTCGCCATTCT	84708
rs200773812	snp	C/T	0.000119205	0.00771934	missense	LNX1	GRCh38.p7	4:53481830	CCTGGCGGGACACGA[C/T]GAGGTGAACACGTCT	84708
rs200779003	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53466694	CAGGAGATTATATCC[C/T]GCACCTGGCTCGGAG	84708
rs200781307	in-del	-/AG	0.00018261	0.00955363	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498857	GACTGAAATGGACAA[-/AG]AGTGTTTATTTAAGA	84708
rs200783327	in-del	-/T	0.492037	0.0625946	intron-variant	LNX1	GRCh38.p7	4:53612706	CAGCTAATTTTTGTA[-/T]TTTTTTTTTTTGTAG	84708
rs200784104	in-del	-/GTT			intron-variant	LNX1	GRCh38.p7	4:53464523	TGGACAATCAGTGTT[-/GTT]ATAAACTCATAATTC	84708
rs200811374	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53634266	GCTTTTTTTTTTTTT[G/T]AGATGGAGTCTCTGT	84708
rs200825695	snp	A/G			intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53559415	GTAGAAAGAAGTTAG[A/G]TTTGATATGTAGGTG	84708
rs200834035	in-del	-/A			intron-variant	LNX1	GRCh38.p7	4:53590079	TGGTGGCCAAACCCC[-/A]CCCCCTTAAACTCAC	84708
rs200836210	in-del	-/T			intron-variant	LNX1	GRCh38.p7	4:53590085	GCCAAACCCCCCCCC[-/T]TAAACTCACAAGCTT	84708
rs200839375	in-del	-/T			intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53462365	GCCAAGTGTTAACTA[-/T]GTTATAATTGCCATA	84708
rs200842570	snp	C/T	0.000148267	0.00860879	missense	LNX1	GRCh38.p7	4:53478673	CTGCGACGGTCATGC[C/T]GAGAGATTCACCGGG	84708
rs200893538	in-del	-/C			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53515508	CACTTCAATTTAAGG[-/C]CCCCACCCCACCAAA	84708
rs200903290	snp	A/G	0.000296839	0.0121791	intron-variant	LNX1	GRCh38.p7	4:53476745	AGGGATGTTGTGTTT[A/G]GACTTACCGTGGTAA	84708
rs200905735	snp	C/G/T	0.000198214	0.0099534	missense	LNX1	GRCh38.p7	4:53478736	AAGTAATTGTAGGAT[C/G/T]GAGGGGCTGAAGGCA	84708
rs200908824	in-del	-/CAG			intron-variant	LNX1	GRCh38.p7	4:53491277	TTCAAAGTGAGAAAA[-/CAG]AAAAAAAAAATCTTG	84708
rs200910255	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53536330	AGATTCTCACTCCAC[A/T]TCTTCAAGAGGGGAC	84708
rs200916039	in-del	-/A	0.0197687	0.0974348	intron-variant	LNX1	GRCh38.p7	4:53496488	CAGGATCCTGTCTTT[-/A]AAAGACTGCTCTGCT	84708
rs200927489	in-del	-/C	0.0111196	0.0737302	upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53592416	GCAGCTGGGAGGTAT[-/C]CCAGGACTGTTAAAC	84708
rs200936024	in-del	-/GTGTGA			intron-variant	LNX1	GRCh38.p7	4:53652017	CAATTTGATGTGTGT[-/GTGTGA]GAGAGAGAGAGAGAG	84708
rs200944901	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53495843	GCCACCACGCCCAGC[C/T]GAGTAATGTTCTTAC	84708
rs200983628	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53526456	GAATGCCTACTTTTT[A/C]GAAGAAATTTTAAAG	84708
rs201002899	snp	A/C			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53515517	TTAAGGCCCCCACCC[A/C]ACCAAAAAAAAAATG	84708
rs201006267	in-del	-/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53515509	CTTCAATTTAAGGCC[-/G]CCCACCCCACCAAAA	84708
rs201007329	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53549474	GGAGGTTGAAAGAAA[A/C]TTAAGAGATGTGGCA	84708
rs201017055	in-del	-/ACAC			intron-variant	LNX1	GRCh38.p7	4:53529103	TAAGAGTCCTGACCA[-/ACAC]ACACACACACACACA	84708
rs201020607	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53563691	AGGCATCTGTCACCA[C/T]GCCTGGTTAATTTTT	84708
rs201022410	snp	A/T	1.92502e-05	0.00310238	missense, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573785	TCCATGGGACAGAAG[A/T]CCTTCTCCACCAGGA	84708
rs201038343	in-del	-/TT			intron-variant	LNX1	GRCh38.p7	4:53557066	GATTGCTAGAAGTCA[-/TT]CACATTAGTCTATAA	84708
rs201062570	snp	A/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	LNX1, LOC101928879	GRCh38.p7	4:53577576	TCCTCCAGCTCTGCC[A/T]TTACTATTATTATTA	84708
rs201062827	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53620914	TGACTTTTGAGCTTC[A/C]AATAAACTTAGAAAG	84708
rs201064242	in-del	-/AAC			intron-variant	LNX1	GRCh38.p7	4:53583974	AACAACAACAACAAC[-/AAC]GACAAATGAAGGCAG	84708
rs201107535	in-del	-/CTAATCTT	0.0244538	0.107838	intron-variant	LNX1	GRCh38.p7	4:53571079	GTCTCGCTCTGTCAC[-/CTAATCTT]CTAATCTTGGCTTAC	84708
rs201113367	snp	C/G	3.32657e-05	0.0040782	synonymous-codon	LNX1	GRCh38.p7	4:53481780	ATTGCTGTTCCAGCC[C/G]GCTTCCTGAAAGATG	84708
rs201126543	snp	C/T	0.000118873	0.00770858	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507994	GACTCACCCCTAGTT[C/T]GGTTGCTCCGGCCAG	84708
rs201131725	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	LNX1	GRCh38.p7	4:53654287	CTTTTCAACCTTATC[A/G]CATGAAATAAAAAAC	84708
rs201132714	snp	C/T	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53467102	ACCCCCCAGTAGGGG[C/T]GGACTGACACCTCAC	84708
rs201149126	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53568532	ATGACAAACCTACAG[A/C]CAATATCATACTGAA	84708
rs201157691	snp	A/C/T	6.60059e-05	0.00574449	missense, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498682	GCCGGCCGTCTCTGG[A/C/T]GATCACCCCATCACG	84708
rs201159053	snp	C/T	9.88419e-05	0.00702931	missense	LNX1	GRCh38.p7	4:53496240	ATCACATGAAAGCTG[C/T]CATCTCGGGGTCTGT	84708
rs201161795	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53636205	TTTTTTTTTTTTTTC[A/G]TTTTCAGGGGAGAAG	84708
rs201170379	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53528688	GTGGATAAGGGGGGG[A/C]CTACTGTATAGCCTA	84708
rs201201503	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53469117	TCAGCAAATGTAAAA[C/G]AACAGAAATTATAAC	84708
rs201213236	in-del	-/C	0.0275645	0.114116	upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53593213	AAAGGCCCCCCTCTT[-/C]ACGCGGACAGGGTGT	84708
rs201258597	snp	C/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53595976	TCATCTCTACAAAAA[C/G]CTCTTTGGCTATCTT	84708
rs201301020	snp	C/T	3.32779e-05	0.00407895	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507481	CGTGCTGAGGAATAG[C/T]GACAGGAGGAACAGT	84708
rs201312756	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53541149	CTCAAAAAAAAAAGA[A/G]AAAAAAAAAAGAAAG	84708
rs201327120	in-del	-/T	0.35207	0.228214	intron-variant	LNX1	GRCh38.p7	4:53613347	CCTGCTTTCCAGGAA[-/T]TTTTTTTTTTTAACT	84708
rs201366924	in-del	-/A/AA			intron-variant	LNX1	GRCh38.p7	4:53583562	TACAGAAAAAAAAAA[-/A/AA]CCCTTTTAAATGGTC	84708
rs201385122	snp	A/C			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53512386	TGGTAATTAAAAAAA[A/C]CTGCCAACACAAGTA	84708
rs201391314	in-del	-/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53502313	ACCTCTGAGATATTG[-/T]GGGTTTGGTTCCAGA	84708
rs201394450	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53475689	TGAAGGCCAACAGTT[A/T]ATGCTCTCATGCAGG	84708
rs201461021	snp	A/G	9.91097e-05	0.00703882	intron-variant	LNX1	GRCh38.p7	4:53476722	ATCGTTTTCTCCCAC[A/G]CCCCTACAGGGATGT	84708
rs201463731	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53608317	AATAAATGAACATGC[A/G]CTTTTTAAAAGAAGA	84708
rs201484541	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53570610	CATGGCACATGTATA[C/G]GTATGTAACTAACCT	84708
rs201491701	in-del	-/T	0.0154538	0.0865337	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53593671	AAAAATAATATGGGC[-/T]TTTTTTTTTGGGCCA	84708
rs201496774	in-del	-/G	0.0228947	0.104514	intron-variant	LNX1	GRCh38.p7	4:53538451	AGGAGGCAGGCATGA[-/G]GGGTGGCATGAGACT	84708
rs201500451	in-del	-/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53501298	TTTTTTTTTTTTTTT[-/G]TGGGGGTGGGGGGAC	84708
rs201530493	snp	A/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53540883	GGCTGACGCCTGTAA[A/T]CCCAGCACTTTGGGA	84708
rs201535637	snp	A/G	0.315516	0.241263	intron-variant	LNX1	GRCh38.p7	4:53565641	CAACAGAACAAAGCT[A/G]GACAGAGAATGACTT	84708
rs201541285	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53516503	TGATTCTGCTTGGGG[C/T]AATTGGAGAAGGCTT	84708
rs201585301	in-del	-/GGGCACAAGACAGGG			intron-variant	LNX1	GRCh38.p7	4:53568580	ATTCCCTTTGAAAAC[-/GGGCACAAGACAGGG]GGGCACAAGACAGGG	84708
rs201589105	in-del	-/G			intron-variant	LNX1	GRCh38.p7	4:53541986	ATGACACATGGCCCT[-/G]GGGAATAGAATTTGA	84708
rs201590969	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53535142	TAAAGGTTTAGACTT[C/T]TTTAAGGAACACAAA	84708
rs201597301	snp	G/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53568416	GATTATCTCAATAGA[G/T]GCAGAAAAGGCCTTT	84708
rs201633776	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53466723	AGGGTCCTATGCCCA[A/T]GGAGCCTTGCTCATT	84708
rs201643861	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53590515	TATTGGGCTGTCAAG[A/G]TACAGGCTGTGTGAT	84708
rs201644628	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53549475	GAGGTTGAAAGAAAC[A/T]TAAGAGATGTGGCAA	84708
rs201663477	snp	A/G	0.00299544	0.0385843	intron-variant, missense	LNX1, LOC101928879	GRCh38.p7	4:53576221	CCAGTGCCCTGGCTC[A/G]CTTCCTGCAGCCGAG	84708
rs201670080	in-del	-/CC	0.43309	0.17023	intron-variant	LNX1	GRCh38.p7	4:53625841	GACCCAGCAATTCCA[-/CC]CCGTGTGTGTGTGTG	84708
rs201685096	snp	C/T	0.000358944	0.0133919	intron-variant	LNX1	GRCh38.p7	4:53481884	ACAGGCATTAGCCAC[C/T]GTCAGTTTCCATCCA	84708
rs201718120	in-del	-/TATC			intron-variant	LNX1	GRCh38.p7	4:53477200	TAAAGCACAGCTATC[-/TATC]GGTGTTTTACACAAG	84708
rs201764158	snp	G/T	0.00398564	0.0444627	intron-variant	LNX1	GRCh38.p7	4:53553552	ATATAGGGCCAGAAA[G/T]ATGAGAAGGCTGTTT	84708
rs201765779	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53606312	ATGAACACCTCTATG[A/C]ACACAAGCTAGGAAA	84708
rs201792197	snp	A/C/G	0.00111737	0.0236104	missense	LNX1	GRCh38.p7	4:53496349	GCTGCCGCAGGAGAC[A/C/G]CACAGCGTAGTTGTG	84708
rs201804292	snp	A/G	1.64863e-05	0.00287104	missense	LNX1	GRCh38.p7	4:53476939	GCCTCACTCCGGCTG[A/G]CCTCTGTCAGTTCGA	84708
rs201839868	in-del	-/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53518789	CCTGGTGGCTGATTA[-/T]TTTGGGGGGCAACTG	84708
rs201852981	snp	A/G	0.0103295	0.0711199	intron-variant	LNX1	GRCh38.p7	4:53470950	AGTGCCATCCCCATC[A/G]AGCTACCAATGACTT	84708
rs201855102	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53490139	ATTGATTCATATAAG[A/G]AAAAAACAATTACAC	84708
rs201873280	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53472274	TTCTCACTCATAGGT[C/G]GGAATTGAACAATGA	84708
rs201886907	snp	C/T			intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53574995	TCGTTTTTTTTTTTT[C/T]TTTTTAGACGGAGTC	84708
rs201887408	in-del	-/T			intron-variant	LNX1	GRCh38.p7	4:53615710	ATACAGAGCCTTGGA[-/T]TTTTTTTTTACTACC	84708
rs201951948	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53470376	TGACAAACCCACAGC[C/T]AATATCATACTGAAT	84708
rs201956700	snp	C/G/T	0.000265376	0.0115165	intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573600	GGGGGTGGGACTTAC[C/G/T]GGCTCGCTGATGGGG	84708
rs201971090	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53634523	TGCTGGGATTACAGG[C/T]GTGAGCCACCGCCCC	84708
rs201977041	snp	A/C			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53515518	TAAGGCCCCCACCCC[A/C]CCAAAAAAAAAATGA	84708
rs201983233	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53545414	AAGCAAATCCATCTC[C/T]ATGACAACACAGTAG	84708
rs202028809	in-del	-/TC			intron-variant	LNX1	GRCh38.p7	4:53534416	GCTGAGGCAGGAGGG[-/TC]TCTCGAGCCTAGGAG	84708
rs202074624	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53464494	CAACATGAAAAAGAT[C/G]TTTATGGGAGATTAA	84708
rs202114434	in-del	-/A			intron-variant	LNX1	GRCh38.p7	4:53541331	TCATGTCAAAAAAAA[-/A]GAGGTTGGGCTGAAA	84708
rs202139713	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53570579	AAATGACGAGTTAGT[G/T]GGTGCAGCACACCAG	84708
rs202145063	in-del	-/GCCA			intron-variant	LNX1	GRCh38.p7	4:53616719	AAACCTTATCAATAT[-/GCCA]GCCATTCACTTTAAT	84708
rs202162185	snp	C/T	0.00199792	0.0315431	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508172	CGTCTGGACAGCCAT[C/T]TTGTGAGCGCCTCTT	84708
rs202180102	snp	C/T	1.6625e-05	0.00288309	intron-variant	LNX1	GRCh38.p7	4:53478756	GGCTGAAGGCACAGA[C/T]GGAAAAACATGGCAC	84708
rs202186179	snp	C/T	0.000429176	0.0146425	intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573580	GGGGTCCAGCTGTCC[C/T]GCTTGGGGGTGGGAC	84708
rs202229204	snp	A/C/T	6.84381e-05	0.0058493	intron-variant	LNX1	GRCh38.p7	4:53481698	CCTTGCAGGAGCAGG[A/C/T]GACCTGCCCTAGAGG	84708
rs207464698	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53561777	CAAATTATTGAACAA[C/T]GAACTCTGTATTCAT	84708
rs207464699	snp	C/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53599706	CCACAGCCTTATCTT[C/G]GCTCTTATCCATGAA	84708
rs367553282	snp	C/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53597175	CCTATGTATGCTTTG[C/T]AATGCTAGCTGCACT	84708
rs367566829	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53544338	AGCTGGGACTACAGG[C/T]GCATGCCACCATGCC	84708
rs367568339	snp	A/G			intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53558430	CCAGTTTGCTATAGC[A/G]ACACTGTAAGAAATT	84708
rs367581810	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53570342	TGTAGCCATAAAAAA[G/T]GATGAGTTCATGTCC	84708
rs367591653	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53502173	TGGCATTGAGCTAAG[C/T]TACTTGAATGCATTT	84708
rs367622298	snp	A/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53516870	ACAGGAGAGGGGAGG[A/T]GGTTTCAGAAGGAAT	84708
rs367628853	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53522409	CCAGGCTTGGTGCTC[C/T]TATGACTCTATACCA	84708
rs367679321	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53648167	ATTTTTCATTTTTTG[G/T]TGAACCACCATACCA	84708
rs367685755	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53606705	CAATGCAAAAATCCT[C/T]AATAAAATACTGGCA	84708
rs367689951	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53630970	GGGCTTACCTGGTTG[C/T]AGAGGTCAACCTGGG	84708
rs367705327	snp	C/T	0.000153988	0.00877328	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461425	ATTTTTGATTAGTCA[C/T]TATTATTACCTAATT	84708
rs367707408	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53488440	TCTTTTCAAGTCATC[C/T]AAAAAATGTAATAAG	84708
rs367712145	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53582096	TAATTTTAGAAACCT[A/T]AGAATATCAAAACTG	84708
rs367712185	in-del	-/AACAACAAC			intron-variant	LNX1	GRCh38.p7	4:53583933	AACTGACCCCCTGCA[-/AACAACAAC]AACAACAACAACAAC	84708
rs367739278	snp	C/T	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53481580	GTCTTAAATATGGGA[C/T]TTTGGGCTTTTAGTT	84708
rs367740196	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53615958	CAATTATTATTGACT[A/G]CAGTCACCCTGTTGT	84708
rs367743562	snp	C/G			upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53592744	TTGGGGTTTGGTTTG[C/G]GGGAGGGTGGAGGAA	84708
rs367772068	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53620576	TGAAGACTGTGGACC[A/G]GAAGCAGTTGCTTGA	84708
rs367789342	in-del	-/T			intron-variant	LNX1	GRCh38.p7	4:53634265	GGCTTTTTTTTTTTT[-/T]GAGATGGAGTCTCTG	84708
rs367802598	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53614580	TTCCATCACAGGTAC[A/C]CAGGAAAATGACCAA	84708
rs367812617	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53633424	GGATTTCTTCATCTC[A/G]TTTTTTACAGTGTTT	84708
rs367815411	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53554426	CATGCCTAAGTGATC[C/T]GCTAAATTGGACACA	84708
rs367832733	snp	A/C			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53594638	GATATTACTCCAGGC[A/C]CACTAGCAGTTGGTT	84708
rs367838246	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53526476	AAATTTTAAAGCCCA[A/G]TGAAAACCCTTGGCC	84708
rs367852101	in-del	-/AATA/AATAAATA	0.487995	0.0765403	intron-variant	LNX1	GRCh38.p7	4:53570664	AACTTAAAGTATAAT[-/AATA/AATAAATA]AATAAATAAATAAAT	84708
rs367860926	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53565615	TCCAAAGGAACGCAG[C/T]TCCTCACCAGCAACA	84708
rs367928776	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53648294	TTTTTTAACTTGATA[A/G]TAGCCATGCTAATGG	84708
rs367979533	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53648373	ATTAGTGATGAGGAT[A/C]TTTTCCTGTGCTTAT	84708
rs368007280	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53505916	TAATGGAAGGGAGGT[A/G]AAAGAAAGATATACA	84708
rs368028008	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53620780	TCCTCCCAGTGCTTA[C/G]AGTCCAGTGCATTTG	84708
rs368055555	snp	A/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53594877	CCACCATGCCCTGCT[A/G]GTTTTTAAATTTTTT	84708
rs368072499	snp	C/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53601886	CTCCAAACTGGTTAC[C/T]GCTGTTTCTCCCTGC	84708
rs368088715	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53638068	AGTTTCAGAGGGAAA[C/T]ATGAATGACCACTTG	84708
rs368094011	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53631879	TTTTTTTTTAAGTCC[C/T]TGAGAATCCTTGACT	84708
rs368096605	snp	C/T	4.94531e-05	0.00497234	intron-variant	LNX1	GRCh38.p7	4:53557854	ATAAACACACAGGCA[C/T]GGACAGAGAGGGGAC	84708
rs368127516	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53609241	TTTACCTATGTAACA[A/T]ATATGCACATGTACC	84708
rs368130481	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53532509	CTGGTGACACAAAAC[C/T]GTCAGCTGCAAAATG	84708
rs368158737	multinucleotide-polymorphism	CA/TG			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53513277	ATGTATTATGCTTTA[CA/TG]GATGTGGTCTCATTT	84708
rs368180873	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53565374	AACTGGGAGGCACCC[C/T]CCAGCAGGGGCACAC	84708
rs368180921	snp	A/G	0.00676609	0.0577691	intron-variant	LNX1	GRCh38.p7	4:53532928	CTGGGAGCCTGCTAG[A/G]CTGATGCTCTGTCCT	84708
rs368184950	snp	C/T	0.00517822	0.0506191	intron-variant	LNX1	GRCh38.p7	4:53587795	AAGCCAGGAAATCAC[C/T]GCTCCAGGAAGACCC	84708
rs368204679	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53517977	CCACACACGGCTTCC[C/T]CTCATTAGCCCCTTT	84708
rs368208857	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53554023	GAGAAACAGCTTAGC[A/C]CCTAGCCTGTCCCAG	84708
rs368228379	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53468931	CATTAGACAGATCAA[C/T]GACACAGAAAGTTAA	84708
rs368232092	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53539784	CACTATCAAAGATAT[G/T]GCTCGCTTCATATTT	84708
rs368283407	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53495993	TGTCCGGGGTTTCTG[A/C]CTGGGATCCTGGAAT	84708
rs368294521	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53553755	CCCATGCCCTGATCT[A/G]TGGATTGGGACTCCA	84708
rs368324239	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53480949	AGATGACTGAAAGAA[A/G]CTCATCAGCATCACA	84708
rs368330504	snp	G/T	0.00358779	0.0422022	intron-variant	LNX1	GRCh38.p7	4:53651334	CATTCCTTGGGCACC[G/T]GACTTGCACCACGCC	84708
rs368365386	snp	A/T	0.000214205	0.0103468	intron-variant, synonymous-codon	LNX1	GRCh38.p7	4:53557879	GGGGACTCACAGTTC[A/T]GAATACAGGAAGTGC	84708
rs368374408	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53492281	GATATTTAGAAGATT[C/T]TTCCAGGCAGAGGAA	84708
rs368391218	snp	C/T	3.41041e-05	0.00412927	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498592	GTTTGCTCAGAAGCA[C/T]TTTTTTATATCAAGC	84708
rs368395398	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53549742	GAAGATGGGTATAGG[A/C]CACATGGAGTTTTAT	84708
rs368419007	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53642095	GGTTTGGTGGTACAC[A/G]CCTGTGATCCCAGCT	84708
rs368427943	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53635964	GCCAGTGATGGGGAA[C/T]TAGAAGCATTAGGCT	84708
rs368447386	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53504545	ATCATGTGTTCACTG[A/G]AAGTAGCACTTTTAA	84708
rs368458600	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53531418	TGGATTGGACAATCT[C/T]TAAGACCCCTAATAA	84708
rs368472958	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53641695	CACTCCCCATTCACC[A/G]GGTCCCCAGGCAAGT	84708
rs368478340	snp	A/G	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53550878	AAGCCAGACCAGGGC[A/G]TAATGGATAGATGGA	84708
rs368480816	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53564240	TGGGCTAAGGGTGAA[G/T]GAAATTCCCAGTCTG	84708
rs368484997	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53544994	GAGTTTGCATTGCAC[A/G]AAGGTGGAGGGAGTG	84708
rs368508357	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53514582	GAACTGCCCCCATGA[C/T]TCATGGATCTCCAAC	84708
rs368519562	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53562560	TAGACAAGTATTGTT[G/T]ACAAATGAAACGCAT	84708
rs368562142	snp	A/C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53639138	CATATACACCATGAA[A/C/G]TACTATGCATCCATG	84708
rs368578125	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53513972	GTCCTCAAACTTGCC[C/T]ACCATGTTCCTACTT	84708
rs368582943	snp	C/T	1.70667e-05	0.00292114	intron-variant, utr-variant-5-prime	LNX1	GRCh38.p7	4:53558006	CCTGGCCACCTTCTG[C/T]CAGCTACAAGGGCCC	84708
rs368587411	snp	C/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53513475	CTCATATCAAACTGC[C/G]CATTCCATGTCATCA	84708
rs368592804	snp	C/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53514661	CAAGATTTGGGTGAG[C/G]ACAGTCAAACCATAT	84708
rs368604988	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53485398	AGACTTGCACATCGA[A/G]TCAACTTGCCAGGCA	84708
rs368609772	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53475911	CTAAGGAGAGATGAT[A/C]TAAGAAATGTCTCCA	84708
rs368610424	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53529816	CCTGGTTCCTAAATG[A/C]ATGACAATCAGAGCC	84708
rs368611299	snp	A/C			intron-variant, nc-transcript-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53501897	CACTCCAGCCCGCCT[A/C]CTCATTGAACATGGC	84708
rs368613125	snp	C/T	3.29728e-05	0.00406021	missense	LNX1	GRCh38.p7	4:53478598	CTCTGCTTATGACTC[C/T]TCCGGGCTCAACACT	84708
rs368654764	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LOC101928879	GRCh38.p7	4:53575501	GGATATGCTTCTGCC[C/T]TCAGGGAGTCCCCAT	84708
rs368664273	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53530884	AATTGTAAAATGAGG[C/T]CAGGCATAGTGACTC	84708
rs368693443	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53515769	AAAGATGGCACAGCA[C/T]GGAGGAAAAAGCACA	84708
rs368724938	snp	C/T	0.00636936	0.0560724	intron-variant	LNX1	GRCh38.p7	4:53651671	ACAACCCTACACACC[C/T]GTGAGCAGGTCACAG	84708
rs368761749	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53610738	AAAAAAAAAAAGAAA[A/T]AAACCAAATCTTCAT	84708
rs368768462	snp	G/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53599016	ACAGATGCAGTTACA[G/T]GAGACAGCAGGCCAG	84708
rs368779316	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53496535	TGTCCAATAACCGCA[A/C]CTTCCAACAGCGTTT	84708
rs368814822	in-del	-/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53520679	ATTCTGTTTACTTTT[-/T]GGCTGGGCATGGAGG	84708
rs368838123	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53485808	TGAGGAGGGGGAGTA[A/T]AGGGGAGACACAGAA	84708
rs368839190	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53634055	GCAAATCAGCTCAAT[A/G]GGGCAGGAAGTATGC	84708
rs368851158	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53551498	GTTTAACTGGTATAT[A/G]AATCCTCAACTGATA	84708
rs368876051	snp	C/T	0.00318978	0.0398085	intron-variant	LNX1	GRCh38.p7	4:53632489	TCAGTCAGACAATGA[C/T]CGACTGACTAGGGTA	84708
rs368890952	snp	A/C/T	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53503009	GATCTCGGCTCACTG[A/C/T]AAGCTCCGCCTCCCA	84708
rs368893611	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53502745	AGAGTCAATCCTCTA[C/T]TAACCTTGCTGTTTT	84708
rs368914513	snp	A/C			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53602679	GAGTCCACAGGACCC[A/C]AGTCAAGGGAAGGCA	84708
rs368922333	snp	A/T			utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460785	ATTAGATGATCATAC[A/T]TTTCCTGACATTTTT	84708
rs368946180	snp	C/T	0.0111196	0.0737302	intron-variant	LNX1	GRCh38.p7	4:53562058	AGAAATCACAACTTA[C/T]TTTTCTTTCATTCAG	84708
rs368950465	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53572850	GCCACAAAGTTAGCA[A/G]AACAAATTGCTTGGA	84708
rs368961690	snp	C/T			nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53603849	ATATCCAGACTATAT[C/T]GGGGCTGTACCAGCA	84708
rs368962271	snp	A/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53513115	AACAATTTTTTTTTT[A/T]AACTCAAAAACCGCC	84708
rs368964234	snp	A/C/G	4.7016e-05	0.00484832	missense, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573689	TGCTCCCTGAATGGG[A/C/G]AGGTCACCAGTAGCT	84708
rs368969660	snp	A/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53500595	AAAGAATTAAAATTA[A/T]TTCTAAGTATGTTAG	84708
rs368974607	snp	A/G	0.0130921	0.0798413	intron-variant	LNX1	GRCh38.p7	4:53564957	GGCTTAAAAAATGGC[A/G]CACCACGAGATTATA	84708
rs368982377	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53530653	ATTCAGAGTAAAAAA[A/T]GTAGTATTATTTAGG	84708
rs369000832	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53469089	GACCACATAGTTGGA[A/G]GTAAAGCACTCCTCA	84708
rs369003698	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53603235	GGCTTCCTTGGGAGC[C/T]GACTCCTCACTGCAT	84708
rs369004252	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53492936	GTGGGCACATGAATT[C/T]GGGAATAGATGGCAT	84708
rs369011995	in-del	-/A/AA/AAA/AAAAAAAAAAAAAAAAAA			intron-variant	LNX1	GRCh38.p7	4:53527051	CTCTTCCCTGCCCCT[-/A/AA/AAA/AAAAAAAAAAAAAAAAAA]AAAAAAAAAAAAAAA	84708
rs369017319	snp	A/C	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53466937	GCACAGACAAACAAA[A/C]GGCAGCAGTAACCTC	84708
rs369040583	snp	C/G/T	0.000613922	0.0175095	intron-variant	LNX1	GRCh38.p7	4:53495997	CGGGGTTTCTGACTG[C/G/T]GATCCTGGAATGACC	84708
rs369058262	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53545110	TTGATCCTTTGTAAT[C/T]TTTCATCAATTAGCT	84708
rs369063630	snp	G/T			upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53593301	GCCACGCCTTCAGCG[G/T]TCTTGCCTTTGGCGA	84708
rs369075994	snp	A/G	0.00398564	0.0444627	intron-variant	LNX1	GRCh38.p7	4:53612840	CAGTGATCTGTGGTC[A/G]TATCACTGCACTCCA	84708
rs369076050	in-del	-/AACAACAACAACAACAAC			intron-variant	LNX1	GRCh38.p7	4:53583957	AACAACAACAACAAC[-/AACAACAACAACAACAAC]GACAAATGAAGGCAG	84708
rs369099268	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53650216	TACACAAATGCATAG[C/T]GCGTGTCACAGTCCT	84708
rs369107035	snp	A/G	0.0225045	0.103662	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519176	CAGGCAGCAAGCATC[A/G]TAGAAGCAGAGGCCT	84708
rs369115896	in-del	-/C	0.00318978	0.0398085	intron-variant	LNX1	GRCh38.p7	4:53466300	GCCAATAATGTTGAA[-/C]TACATACTTAAAGCA	84708
rs369126631	in-del	-/GGGGCACAA			intron-variant	LNX1	GRCh38.p7	4:53568609	GGGGCACAAGACAGG[-/GGGGCACAA]GATGCCCTCTCTCAC	84708
rs369167469	snp	C/T	0.000153988	0.00877328	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508133	CCTCTGGGGAGGGAG[C/T]CGTGGCTGTGAGGCT	84708
rs369187313	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53642705	TCCCTTGCTCTACTC[A/G]CCAAAATCAGCAAGC	84708
rs369210850	snp	G/T			nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53604165	TGAAGTTGCCAAACT[G/T]CTGATTTTTGTTCTA	84708
rs369227276	snp	A/T	0.00318978	0.0398085	upstream-variant-2KB	LNX1	GRCh38.p7	4:53652762	AGGTCCTATAATCCT[A/T]GGCATCTTTTATTTT	84708
rs369229696	snp	G/T	0.00835141	0.0640778	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507173	CTACATACGTGAGAA[G/T]TAGGCTAATCAAAGT	84708
rs369235567	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53628231	GAATAGGAGAAAATA[C/T]ATGCAAACTATGCAT	84708
rs369294756	snp	C/T	1.66194e-05	0.00288261	missense, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461498	ATGAAAAAAGGTTTG[C/T]TTCCATTGTATTCTT	84708
rs369336528	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53563035	CATGGTAAAAACCTG[C/T]CTCTACTTAAAATAC	84708
rs369343580	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53552270	TTTGAAAAGCGAGTC[A/C]CAAACTAACTGTGCA	84708
rs369353200	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53631239	GGGTGGGATAATGCA[A/G]GAGCCTGGACTCTTT	84708
rs369373384	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53527073	AAAAAAAAAAAAAAA[A/C]TAGAAGAACAAAACC	84708
rs369410082	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53474166	TCCTAATTGGCAGTG[A/G]ATACAACGATGGTGC	84708
rs369415881	snp	G/T	1.72558e-05	0.00293728	missense, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573863	AGGGGGTCCAGCAAA[G/T]CCTGCAGGCAGATGT	84708
rs369417673	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53634410	TGCCAGACCTGGCTA[A/C]CTTTTTGTATTTTAG	84708
rs369428500	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53617841	TGATAAGTAAATGCT[C/T]TATTATTTGTTAACC	84708
rs369466761	snp	A/G			intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53499646	GCTTGCTTATTGAGA[A/G]GTAAAAAACAGAACC	84708
rs369503956	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53573321	AGATGGATGGTGGTG[A/G]TAGTTGCACAATACA	84708
rs369512854	in-del	-/ATCT			intron-variant	LNX1	GRCh38.p7	4:53479645	ATGACTTTTCTATCT[-/ATCT]TTTTTCGCCATTCTC	84708
rs369519134	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53633839	GCTGTGGGACTTTGG[A/G]GAGATTGCATAACCT	84708
rs369527761	snp	A/C			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53514827	TTTCAAGCTAAGGGA[A/C]CTGAACCATGAACAA	84708
rs369556334	in-del	A/GG			intron-variant	LNX1	GRCh38.p7	4:53528685	CCTGTGGATAAGGGG[A/GG]GACTACTGTATAGCC	84708
rs369570747	snp	A/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519655	CTGTGTCTGTCAAGG[A/T]ATCTGACACACACAC	84708
rs369583472	snp	C/T	0.00636936	0.0560724	intron-variant	LNX1	GRCh38.p7	4:53646628	AACTTGAAATTTGAA[C/T]TTTTATATGAAATCT	84708
rs369590952	snp	A/G	0.000150204	0.00866484	missense	LNX1	GRCh38.p7	4:53481751	CTCTCCCCTGGCCCT[A/G]GGGACCAGCTGCCAT	84708
rs369592789	snp	A/G			intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573549	GTTGGAAGCCCTCAG[A/G]AGACTGGGGGGTGGA	84708
rs369594729	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53466261	TATATTCACCATCTA[C/T]AAATAGGCTACTTCT	84708
rs369611212	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53540663	CTCCAGCCTGGGCAA[C/T]AAGCAAAGCTCTGTC	84708
rs369615830	snp	C/T	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53541610	TGAATAGTTCTGACT[C/T]GAGACAAGAACAATA	84708
rs369633991	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53555991	TTTGTGTAGGAATAG[C/T]AGGAATCTGTAGTCA	84708
rs369665869	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53485944	TTACTGCAAGAAAGA[A/G]GTAAGACAGCTTCTC	84708
rs369692642	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53618445	AGCTCTGTTTTTGCA[A/G]GTGGCTTTCTACTCA	84708
rs369705482	snp	A/C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53521381	CAAAGTGCATTCCAT[A/C/T]GCATTCTCAGAATAA	84708
rs369724914	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53578708	TTTATCTTTTCCCTT[C/T]CTTTCTTTTTCTTTC	84708
rs369736491	in-del	-/CA			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519686	ACATGCGCGCACATG[-/CA]CACACACACACTCCT	84708
rs369759079	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53615076	CAAATGAATTAATTG[C/T]TGAAAGAAACAGTAG	84708
rs369759869	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53646464	TATCTTACTTATCTG[C/T]CTACTTGGTTATTAT	84708
rs369778097	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53477368	CTCCAGCATTTGCAC[A/G]GAGCCAGGCATGTAG	84708
rs369790580	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53531594	TTTAAGTTCTTCCTG[C/T]TCTGATGCTTCTCCA	84708
rs369793229	in-del	-/G			intron-variant	LNX1	GRCh38.p7	4:53547920	CAAGAACCTGACAGG[-/G]GACCTACCAGTTGTG	84708
rs369861663	snp	C/T	0.00874735	0.0655527	intron-variant	LNX1	GRCh38.p7	4:53560599	CTCTTTAAAGGAAGG[C/T]GTCTCCATTGGCACA	84708
rs369869240	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53631876	CTTTTTTTTTTTAAG[C/T]CCTTGAGAATCCTTG	84708
rs369871241	snp	A/C			upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53592845	CAGTCAATAGCTCGC[A/C]AAGCAAGGGGGAGGA	84708
rs369871933	snp	G/T	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53466652	CCTAATACTGTGCTG[G/T]TCCAATGGGCTTAAC	84708
rs369874848	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53527681	CCTGAACTTTGCACC[C/T]TCACTGGATTGGTGG	84708
rs369900253	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53564912	GGGAAAATCAGGTCA[C/T]TCCCACCCGAATACT	84708
rs369944320	snp	C/T	0.00874735	0.0655527	intron-variant	LNX1	GRCh38.p7	4:53584060	GGGAAGAGCTGATAT[C/T]AGAGGGGTATGGAAA	84708
rs369970352	snp	C/T			intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53559291	GTGCAGATGAACAAC[C/T]TTGATAAAACATGGG	84708
rs369973193	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53581738	TGCGTCCCTCCCACA[A/G]CATGTGGGGATTATG	84708
rs370002308	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53530587	AATTTAGCATATGTA[G/T]CAAGTATTTTTAAAA	84708
rs370003712	in-del	-/AG	0.00199481	0.0315187	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53602792	CAGTGTGAAGGAAAC[-/AG]AAAGTCTGTACATCC	84708
rs370033584	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53471803	TACCATCTCACACCA[A/G]TTAGAATGGCGATCA	84708
rs370072303	snp	G/T	0.00398564	0.0444627	intron-variant	LNX1	GRCh38.p7	4:53613618	CCAGCTCCACCCATA[G/T]TCCCACAAAAGACAT	84708
rs370099678	snp	A/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53601287	ATATCAGTGCCAGCC[A/G]TCAGCCCAGGGTGGC	84708
rs370129787	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53570548	AGGGATAGCATTGGG[A/C]GATATACCTAATGCT	84708
rs370137179	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53472038	AAGACACATGCACAC[G/T]TATGTTTATTGCGGC	84708
rs370140283	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53532650	GAAAATAACATTCCC[C/T]ATGTGACCATTTGGA	84708
rs370175649	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53584119	AGCTGAAAAACAATT[C/T]CAAAAAGTGTTTATG	84708
rs370228515	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53544673	TCTAAAGAAAAAAGT[G/T]TGCAGGGGGCGAAGA	84708
rs370238417	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53612963	TGAATGAGTAAAGCA[C/T]AATGCAGTGAAAAGT	84708
rs370247973	snp	A/G	0.00478085	0.0486577	intron-variant	LNX1	GRCh38.p7	4:53468242	ATATCCAGCCAAAAT[A/G]AGCTCTATAAGTGAA	84708
rs370284853	snp	A/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53600734	TTTATTTTTATTTTT[A/T]TTTTTTCAATTTTTG	84708
rs370303260	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53638142	AGATCTTGTCATTGG[G/T]CATATTTTGTGTCTA	84708
rs370305004	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53572992	CAAGGGTCAAACTGG[G/T]GCACCTTTTTTTCCT	84708
rs370330664	snp	C/T	0.000234639	0.0108289	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508263	AGGTGAAGAAGAGCT[C/T]TGGCTCTGCTGCCAT	84708
rs370331844	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53485019	GAACAGAACAAAAAT[A/T]AAAAGCCCAGGAAAC	84708
rs370344275	in-del	-/AT			intron-variant	LNX1	GRCh38.p7	4:53545802	GACTTCAGAGGCCAC[-/AT]TTTTTTTTTTTTTTT	84708
rs370345536	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53637725	ATTACATAAACCAAA[A/G]CACAGCCAGTTTCTG	84708
rs370366722	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53644052	TCAAAAGCAAAACCC[C/T]GTGGGTAGACTGCAC	84708
rs370372262	snp	A/G			upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53593338	GGATCCAACTTGGGA[A/G]GGGATCACAGGCTTC	84708
rs370379641	snp	C/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53538518	GTTGAAAAACCACTC[C/G]ATTACTCTTCAGGTA	84708
rs370430045	in-del	-/AC			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53515513	CAATTTAAGGCCCCC[-/AC]CCCACCAAAAAAAAA	84708
rs370432543	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53561429	GATGGGGTTTCACTG[C/T]GTTGGCCATGATGGT	84708
rs370440021	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53606093	GACAGGAAATAATCA[A/C]AATCAGAGCTGAACC	84708
rs370457052	snp	C/T	3.2963e-05	0.00405961	missense	LNX1	GRCh38.p7	4:53476933	CACAAACAGGGACT[C/T]	84708
rs370464725	snp	C/T	1.74272e-05	0.00295183	missense, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573980	AGGGGTTCAGGATCG[C/T]TGGCAGACTCTGGCT	84708
rs370491577	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53475071	CCACACCCAGCCCAG[A/T]CTACTTCCAGCAAAA	84708
rs370527617	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53535371	CCATGACACAAAACA[A/T]ACATTTTGATGTTGT	84708
rs370537618	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53564100	AAAAAGGTGACTCAC[C/T]TTCAGTCAGTTTTGG	84708
rs370543661	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53582094	GTTAATTTTAGAAAC[A/C]TAAGAATATCAAAAC	84708
rs370569537	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53629896	TATCCTCTATATGTA[C/T]GCACAATAAAGACAA	84708
rs370583967	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53484056	CCCTCTACCATGTAA[G/T]GACAAAGTGAGATGG	84708
rs370608041	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53502896	TGCCTCTACACTCAT[C/T]CAAGTTTTATTATGA	84708
rs370618910	snp	C/G	0.00398564	0.0444627	intron-variant	LNX1	GRCh38.p7	4:53465122	ATTGAAAAACATCTT[C/G]CATTTTTTTCCTTGC	84708
rs370659059	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53651146	ATGCTCCTCTCCCCT[C/T]GGCTCTGCCACATGG	84708
rs370669789	snp	A/G	0.000164427	0.00906568	utr-variant-5-prime, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53574018	GATGGATTGGAGAGC[A/G]GTATAACAGGAAACT	84708
rs370672561	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53619390	GGCAATCACTAACCT[A/G]ATTTCTGTTTTGTGA	84708
rs370678208	snp	A/C/T	0.00953873	0.0683987	intron-variant	LNX1	GRCh38.p7	4:53568800	CCTTAAGCTGATAAG[A/C/T]GACTTCAGCAAAGTC	84708
rs370682663	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53581779	TACAAGATGAGATTT[A/G]GGTGGGGACGCAGCC	84708
rs370692048	in-del	-/TT			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53502514	CTTGTTGTAATCTTT[-/TT]GCTGGTAGAGAGTCT	84708
rs370694474	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53509235	GCAGAAATCATATCA[C/T]GAGCCCCTTTAGGAA	84708
rs370703061	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53529152	ACACATGCACACACA[C/G]AAAACAACACGAGAA	84708
rs370707109	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53542936	GCCAGCTCCTCTAAC[A/G]TGGTTCTCACTTGCT	84708
rs370738649	in-del	-/ACG			intron-variant	LNX1	GRCh38.p7	4:53583972	ACAACAACAACAACA[-/ACG]ACGACAAATGAAGGC	84708
rs370766966	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53634433	TATTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT	84708
rs370769248	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53606130	AACTGGGAAAAACCA[C/T]ACACAAACCCAACAC	84708
rs370783888	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53529559	CTGGAAGAAACAGTC[C/T]ACCCAGTAAAACATG	84708
rs370799507	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53521452	GGTGTCACAGGCCCT[C/T]CTGGATATGCTGCAT	84708
rs370822390	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53515898	GTGTCTTAATTCCTC[C/T]GAGCCTTGTTTCTCA	84708
rs370832025	in-del	-/CTTT			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53594710	TTCTTTTCTTTCTTT[-/CTTT]TTTAATTTTTTTTTT	84708
rs370847216	snp	A/G	1.64732e-05	0.0028699	missense	LNX1	GRCh38.p7	4:53496106	GGTCATTCTCCTCAA[A/G]CTGACCATGTCGATA	84708
rs370857392	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53479203	GCCATGGAGGAATCT[G/T]AAGCACACAGAGTGA	84708
rs370923970	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53563553	TTTTTTTTTTTTTTT[G/T]AGACAGAGTCTCGCT	84708
rs370932377	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53466707	CCCGCACCTGGCTCG[A/G]AGGGTCCTATGCCCA	84708
rs370939193	snp	C/G/T			intron-variant	LNX1	GRCh38.p7	4:53635016	TTTATTTTTTGTACG[C/G/T]AAGAAGTCTCACTAT	84708
rs370947476	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53629242	GCTACCGAAATAGAG[A/G]GGTGGCTAAAGGTCC	84708
rs370992742	snp	G/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53596948	GGATTTTTCATTCCC[G/T]TCCTCAAATTTTACA	84708
rs370993413	snp	C/T	0.00835141	0.0640778	intron-variant	LNX1	GRCh38.p7	4:53469883	AAGTCCAGGACCAGA[C/T]GGATTCACAGCCGAA	84708
rs371013012	in-del	-/CT			intron-variant	LNX1	GRCh38.p7	4:53544204	TCTCTCTCTCTCTCT[-/CT]TTTTTTTTTGAGACA	84708
rs371053734	snp	C/T	8.24273e-05	0.00641926	missense	LNX1	GRCh38.p7	4:53496288	CCATTGTTCCTGCTG[C/T]GGAACTTCTGTTCAC	84708
rs371097326	snp	A/C			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53600062	CCCCTCTCCCCAATA[A/C]CATATGCTTTTTAAG	84708
rs371120556	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53613054	GTCTACCTACGATTA[C/T]ATAGCCATGAGTAAA	84708
rs371167938	snp	A/T	0.000127183	0.00797342	missense, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573728	AGTTTGTTGACCAGG[A/T]TGCTGGACTTCTTGC	84708
rs371170163	snp	A/G			intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461104	GCTGAAGTTAATGCA[A/G]GTTTATCTTAGTGGT	84708
rs371176467	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53513320	TTGTCCTATTAGTTA[C/T]ACCACCTCACTTCAC	84708
rs371185131	snp	G/T	5.01182e-05	0.00500566	synonymous-codon, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461455	TCTTCCATCATTGTA[G/T]GCTGGTGTTCCTTCA	84708
rs371190686	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53586584	TACCAAAAATGTCCC[C/T]GGTTAATTGGGATAG	84708
rs371197835	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53531362	AGTAAATCACTTTAT[C/T]TTCCAGAGCCACAGT	84708
rs371219326	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53637511	ACTACACCTGTCATT[C/T]CACATGTTATTTACT	84708
rs371225675	in-del	-/TG	0.0807149	0.183963	intron-variant	LNX1	GRCh38.p7	4:53652010	TTTGATGTGTGTGTG[-/TG]AGAGAGAGAGAGAGA	84708
rs371248077	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53625414	AGCAAAGGATTTGAA[C/T]AGATATTAATCCAAA	84708
rs371262219	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53641797	TATTCTTTTTGGTGT[C/G]TGGCTTACTTCACTT	84708
rs371278195	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53564007	TGTGTTGAGGCCCAC[A/G]CCTCCCTGATGTGGG	84708
rs371291378	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53511900	CTTATAATAGAATAA[A/G]AGTTGTTCACAAAGT	84708
rs371312672	snp	A/G	0.0189856	0.0955633	intron-variant	LNX1	GRCh38.p7	4:53471525	GAGCTTCTGCACAGC[A/G]AAAGAAACTACCATC	84708
rs371313684	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53473640	GGTGACAACAGACAC[C/T]AGGGCCTACTTGAGG	84708
rs371315530	snp	C/T	0.00358779	0.0422022	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53499055	CCTTCAAGGCCCTTC[C/T]AATTAAACTCTACCC	84708
rs371349648	snp	G/T	1.65416e-05	0.00287586	missense, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461009	CATTCCTGATGTACT[G/T]CTACCATTGACAGCA	84708
rs371372169	snp	C/G/T			intron-variant	LNX1	GRCh38.p7	4:53635107	AGTGCTGGAATAGCA[C/G/T]GCATGAGCCATGGTG	84708
rs371375451	snp	A/G			upstream-variant-2KB	LNX1	GRCh38.p7	4:53654296	CTTATCACATGAAAT[A/G]AAAAACCAAAATGTT	84708
rs371392337	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53527221	CATATGAATTTCAAT[A/G]AACAGATATTGTTTT	84708
rs371395164	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53619915	ACCATCCCAGTGGGT[A/G]TGGCAAGTCAGCTGG	84708
rs371399015	in-del	-/TGTGTA/TGTGTGTA/TGTGTGTGTGTA	0.170408	0.236992	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53512508	GTGTGTGTGTGTGTG[-/TGTGTA/TGTGTGTA/TGTGTGTGTGTA]TGTGTGTGTGCATGC	84708
rs371407184	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53526426	GGGGAAACCAACAAA[C/T]GCAACTTAGTATCAG	84708
rs371432033	snp	C/T			intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461313	AGAAGTTGAATGCTA[C/T]GTACATACTTTTAAT	84708
rs371436665	snp	A/G/T	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53589170	CTGGACATTTCCCCC[A/G/T]AAAGGCCCATGGAGA	84708
rs371439440	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53633214	TTTGATGAGAAAATG[A/G]ATGTGAAAACCTATG	84708
rs371440807	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53465648	TGGTCCAGAGCTAGT[A/T]GTGTTTATTGCCAAA	84708
rs371441278	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53494899	GTGAAAAAAGCCAGT[C/T]CCCCAAGTCCGTATA	84708
rs371447924	snp	C/T	1.68641e-05	0.00290375	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508036	CTGATTGCTGGCTGC[C/T]CGTCCTCTGCCGAGG	84708
rs371453566	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53633510	ACTGATCCTTGTTCC[A/G]TGGGCTATGGCCAGG	84708
rs371467050	snp	A/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53651980	AAAGATACCTAGATA[A/T]TTCCATCTTTTAGAC	84708
rs371499442	in-del	-/AAA/AAAA			intron-variant	LNX1	GRCh38.p7	4:53610715	CCCGTCTCAAAGAGG[-/AAA/AAAA]AAAAAAAAAAAAAAA	84708
rs371500871	snp	C/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53595329	CTAAATTTAGATGGG[C/T]TGAGACTGTAAAGAG	84708
rs371505959	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53554097	GGTGAATGTTGCTAG[C/G]TGGAGACTGTTAGGG	84708
rs371507321	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53471222	CTTTGACAAACCTGA[C/G]AAAAACAAGCAATGG	84708
rs371509591	in-del	-/G			intron-variant	LNX1	GRCh38.p7	4:53580549	GAGTGGGTAGAGGAG[-/G]AGACACTGCCCTGAG	84708
rs371519456	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53541403	AACTATTCACATAGT[A/G]GAAAGTTCCATGCTT	84708
rs371519596	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53555289	GCTTTGGTGACAACC[A/C]CAGCCAGCCCCTAAC	84708
rs371525082	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53566372	GAAAAGAATTTTCAA[C/T]CCAGAATTTCATATC	84708
rs371530157	in-del	-/CT			intron-variant	LNX1	GRCh38.p7	4:53526646	TCTGCTTGAAATTCT[-/CT]TTTTTCTGCTCAACA	84708
rs371534197	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53571157	CCCAAGTAGCTGGGA[G/T]TACAGGCTTGGGCCA	84708
rs371580008	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519049	GGCCATTTATCATTG[C/T]TGCATGCCTCATAGG	84708
rs371589553	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53621109	ACGGTGACATCACCT[G/T]GGAGCTTGTTAGTGC	84708
rs371602183	in-del	CAAAAATCTAG/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53512234	GGAGAAATTTGGAAG[CAAAAATCTAG/T]TTTTCAATGTAAAAT	84708
rs371617240	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53546966	CCCCTAAGCTAGTTA[A/C]CCCTTTCTCAGCTCA	84708
rs371631200	snp	A/C			intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53558982	GAATGCCACAGAAGC[A/C]CCCAGGACTCTCGCT	84708
rs371644657	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53570386	GGATGAAATTGGAAA[C/T]CATCATTCTCAGTAA	84708
rs371692165	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53627814	GTCTAGAAGTGCTTG[A/G]GTTAGAGCAGAAACC	84708
rs371692276	snp	A/G			intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461890	TAAGACAATGCTTGA[A/G]TATGTATTAGCAAAA	84708
rs371699659	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53644893	GAGGAGGAAGTCTGG[A/G]TAAGGATTACAAGTA	84708
rs371711274	snp	C/T			intron-variant, downstream-variant-500B	LNX1, LOC101928879	GRCh38.p7	4:53578000	GTATATTATGTTATT[C/T]AATCCTCACAAATGG	84708
rs371711749	snp	A/G			nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53603948	TAAATATTTTATGCT[A/G]TACCAATTATTAAAT	84708
rs371712335	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53537172	TATAATAAAAGTGCA[C/T]GTATTAATAAATAAA	84708
rs371723436	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53506423	CACTTATATTGGGGA[A/G]AACATATGGGATCTA	84708
rs371735255	snp	A/C	0.0444908	0.142359	intron-variant	LNX1	GRCh38.p7	4:53639149	TGAAGTACTATGCAT[A/C]CATGAAAAAGAACAA	84708
rs371747609	snp	A/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519389	CCTGTTAATAACAGC[A/T]GTCATAACAGTAACC	84708
rs371751977	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53465877	CTTGGCAATGTGTAT[A/G]CACATTTTTAATCTT	84708
rs371751993	snp	C/T	1.67287e-05	0.00289207	intron-variant	LNX1	GRCh38.p7	4:53478771	TGGAAAAACATGGCA[C/T]ATGAATTCACAACTC	84708
rs371754261	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53492056	CCTCCCAAAATGCTG[A/G]GATTACAGGCATGAG	84708
rs371772139	snp	C/G	0.00398564	0.0444627	intron-variant	LNX1	GRCh38.p7	4:53540411	GATAGTGAGGCTTTA[C/G]TTGAGTGTGCTCCAA	84708
rs371781685	in-del	-/TCT			intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53559859	AGAGATGAGGGTCCC[-/TCT]ATGTTGCCCAGGCTG	84708
rs371791414	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53544103	CCTGCCTAGCTGTCA[C/T]TGGGCTTTTAAATTC	84708
rs371816985	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53553863	TATTTAAAGAAGGAA[A/C]GGCCCTGGTATAAAC	84708
rs371823392	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53539248	GAGCTGAGGGATGCT[C/T]GAGGCCAGGGTCTGG	84708
rs371835646	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53618083	GTGATTTTTAAAAGT[A/G]AACAACTTAGCTTCT	84708
rs371839280	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53564688	ACAGCTCCCAGCCTG[A/C]GCGACACAGAAGACG	84708
rs371840201	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53588283	ATACACAGACCTGTC[C/T]GATACTATCAACTAT	84708
rs371860635	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53482848	GTATTCCTAAAGCTA[C/T]TGAAATACAAAATGT	84708
rs371947963	snp	A/T			intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53559076	TGGCTCGAAGGGATA[A/T]TTACATTCATCACAT	84708
rs371961800	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53636006	CCCTTTGCTAATTCC[C/T]GTGTGACCTTGGGCA	84708
rs371968881	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53530424	TTATCCTCATTTATA[A/G]TTAAAGAAGTGCAAC	84708
rs371969478	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53624469	TCTGCCATGATTGTG[A/G]GTCCTCCCCAGCCAC	84708
rs371976288	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53612046	GGCAAGAAAAACAAG[A/G]ACAAACCAATAGGAA	84708
rs371979692	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53562318	ATTCAACTCAATAAG[C/T]CCATCACCACCCTGG	84708
rs372021685	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53550794	TCTGACTGAAGTTAG[C/T]AGGCAGGAAAAGGAG	84708
rs372025669	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53584389	GAGTTTATCCACAGG[A/C]AAAAAAATGTAAAAA	84708
rs372073514	in-del	-/A			intron-variant	LNX1	GRCh38.p7	4:53586139	AAAGGGCCTCAAGGG[-/A]AAAAAAAAAGGCCAC	84708
rs372078248	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53463332	GAAGCATCCATTCAA[A/G]TTGATATCAGTGTTC	84708
rs372083422	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53474434	AGCAGAAATGAGTAA[C/T]TGCCACAGAGACTGC	84708
rs372127589	in-del	-/TG			intron-variant	LNX1	GRCh38.p7	4:53529142	ACACACACAAACACA[-/TG]CACACACAGAAAACA	84708
rs372135243	snp	A/G	0.00358779	0.0422022	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53502248	ATTACACTGTCCCCT[A/G]TGGCTGCTATGGTCA	84708
rs372142632	snp	A/C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53642677	AATCACAAACACTGG[A/C/T]CTTTTGGAGAGATCC	84708
rs372147808	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53623108	AGGATTCATGATCCT[A/G]GACTGATCACTTGAA	84708
rs372157659	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53631051	AGTGCTCCTGGGCCA[A/G]AAGTACAGTTCTATG	84708
rs372164985	snp	C/T			synonymous-codon	LNX1	GRCh38.p7	4:53476851	GCTGCTGCAGTCTTC[C/T]TGGGGCTCATACTCT	84708
rs372198482	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53493519	CAGTAATACCATCCA[A/C]CACTTGGTCCTCTTC	84708
rs372209583	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53523360	GGCATGGTCTCAGCT[C/T]ACTGCAACCTCTGCC	84708
rs372243142	snp	A/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53602951	GAGACCACTTTTGAA[A/G]CTAGAAAAGGCAAGG	84708
rs372245824	snp	C/T			utr-variant-5-prime, upstream-variant-2KB	LNX1	GRCh38.p7	4:53652497	TGGATGGGGCTGAGA[C/T]GCCCCTGAACTTCCT	84708
rs372348409	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53535832	GTTGGCACAGTTCAT[C/G]AGCATGTCGGGCTGG	84708
rs372352624	snp	A/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53521650	AAAAGAAACAACCTT[A/T]CTCCTTCTATAAAAC	84708
rs372359870	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53570440	AATACCGCATATTCT[C/G]ACTCATAGGTGGGAA	84708
rs372360153	snp	A/G	8.2426e-05	0.0064192	synonymous-codon, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507327	TTTACCTTCAGGGGC[A/G]GTGGTGTTTTCAGAA	84708
rs372360790	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53610261	AGAAAAAATTATCAA[A/T]AGGTAACAAAAAGTT	84708
rs372368114	snp	C/T	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53477680	AAAATATACATCTCC[C/T]CTATTTCCATTTTCT	84708
rs372369981	in-del	-/TGAGAGAGAGAGAGAG			intron-variant	LNX1	GRCh38.p7	4:53652020	TTTGATGTGTGTGTG[-/TGAGAGAGAGAGAGAG]AGAGAGAGAGAGAGA	84708
rs372370274	in-del	-/T	0.0107246	0.0724382	intron-variant	LNX1	GRCh38.p7	4:53584865	CACGTTACTTTGACC[-/T]TTGGCCTTGTTCTGC	84708
rs372377333	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53481211	GCCATATAACATGTG[C/T]TCTCTGGTTTGCCCC	84708
rs372378539	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53492294	TTCTTCCAGGCAGAG[A/G]AACAGCAAGAATGCC	84708
rs372414090	in-del	ACT/CC			intron-variant	LNX1	GRCh38.p7	4:53583563	TACAGAAAAAAAAAA[ACT/CC]CTTTTAAATGGTCTT	84708
rs372444748	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53502860	CTCAAGAAACCACTT[C/T]ATTTGCTCATCCGTA	84708
rs372449313	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53517286	GAAAGAAAGCAGATA[C/T]ATAGTTTAAATATAT	84708
rs372460560	snp	C/T	0.0126979	0.078662	intron-variant	LNX1	GRCh38.p7	4:53564931	CACCCGAATACTGCG[C/T]TTTTCCGACGGGCTT	84708
rs372488277	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53494027	AATACACACCCCAGG[C/T]TCCAGGTACTATTTA	84708
rs372501456	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53482831	GTAACCAAAAACCAC[A/G]TGTATTCCTAAAGCT	84708
rs372512530	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53643873	CACATGGGAAGAATT[C/T]AGTAAGTGACAGTGA	84708
rs372522908	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53640683	CAACAGTAGGAACAA[C/T]TAAGACTGTGTTGTT	84708
rs372523955	in-del	-/T	0	0	intron-variant	LNX1	GRCh38.p7	4:53634265	GCTTTTTTTTTTTTT[-/T]GAGATGGAGTCTCTG	84708
rs372531647	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53490497	TTTCTTCTTAAAAGG[A/G]CCTGGCAAACCCAGG	84708
rs372535613	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53629450	GCTTTGGCCCATTCT[C/T]TTCAAAATGTCCCAG	84708
rs372539229	snp	C/G			upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53593518	AACAGAAAGAAAATA[C/G]AGAAATAAGAGTTAA	84708
rs372541950	snp	G/T	1.66479e-05	0.00288508	missense, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461552	CCCAGACTTCCAGCT[G/T]TGTTTCTTCGTAATA	84708
rs372543467	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53617191	AAAAATAAGACCTAG[G/T]ACCTAGTCTAATAAT	84708
rs372553096	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53462115	ACGTTTGATAAGTCA[G/T]AGAGAAGCATGCACG	84708
rs372557184	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53521409	TAACCAAGATATCTC[C/T]GAGTTTGCCCAAGCC	84708
rs372566811	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53590004	TTGAGGAGAGGTTTA[C/G]ATGCACTTTTATCAG	84708
rs372575029	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53579206	ACAGTGTTTTGGCAG[A/T]TTAGAGTAAGAAAGA	84708
rs372578709	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53606647	AACCTGGCAGACATA[C/T]AATAAAAAAAGAAAA	84708
rs372605579	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53630801	AACGTGGTAGTTCCT[C/T]TAGGAGCAATGATTC	84708
rs372666873	snp	A/G/T	0.0260105	0.111035	intron-variant	LNX1	GRCh38.p7	4:53581697	GCATGGGAAAAACCC[A/G/T]CCCCCATGATTCAAT	84708
rs372697452	in-del	-/TA			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53593748	AAAAAAATGTAATCA[-/TA]AAAATGAACATTGTG	84708
rs372713351	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53556562	TTGAGAGAGGAATGA[A/G]CCTTTTCATAATCTC	84708
rs372774825	in-del	-/AC			intron-variant	LNX1, LOC101928879	GRCh38.p7	4:53575533	CCAGAGGTGACATGG[-/AC]ACACACACAAGTAGG	84708
rs372788192	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53518965	CGGGGTTGGCATCTT[C/T]AGCCTGGAGTTGACA	84708
rs372792932	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53506531	CCTAAGTAACCTCTC[C/T]GTGCCACAGTTTCCT	84708
rs372811982	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53525972	GCAAATTGGACTCTG[C/T]AAATTTCTAGTATCT	84708
rs372851227	snp	A/G	0.000165188	0.00908663	synonymous-codon, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498674	TGGCAGTAGCCGGCC[A/G]TCTCTGGCGATCACC	84708
rs372855121	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53491131	CATGATGAGTAAGAG[A/T]TTTTCTTTTGCTTAT	84708
rs372862221	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53646689	AAAAAATTAAAAACA[C/T]TATGCTGGCCAGAAA	84708
rs372872732	snp	A/G	0.000167695	0.0091553	missense	LNX1	GRCh38.p7	4:53496039	TGAATCAGATGAGCC[A/G]CACTTTCTGGGCTGC	84708
rs372889405	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53467321	AACAGAAAGGGCATC[A/G]ACACCAAAAACCCAT	84708
rs372913825	snp	C/T	0.000265278	0.0115139	intron-variant, utr-variant-5-prime	LNX1	GRCh38.p7	4:53557970	AGCGCCTTCATTCTC[C/T]GAGCAGTGTGCTGCC	84708
rs372924994	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53627587	GTGAATCCTGTCAAA[G/T]GAAAGAAAAGAAAAT	84708
rs372956438	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53572605	GGATAAACAACATCT[C/T]CCAAATTTCCTCTTA	84708
rs372965764	snp	A/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53593818	AAGAACCCTGTGTCA[A/G]GTATCATTGCTATTT	84708
rs372970840	snp	A/G	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53636764	TTACACACCCAATTA[A/G]CTGATTCCATCCTAT	84708
rs372975095	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53523609	GTATGATTTTATATG[A/G]TATGCACATCTCATG	84708
rs372996101	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53527074	AAAAAAAAAAAAAAC[A/T]AGAAGAACAAAACCT	84708
rs373017767	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53534704	AAAACAACCTATTTG[C/T]CTTTGGGGGAGGATG	84708
rs373035833	in-del	-/AG			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53515243	CAGTCAAGACACATC[-/AG]CTCTGCCTTGGCTAG	84708
rs373038810	snp	C/T	0.000153988	0.00877328	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507502	GAGGAACAGTAGTTA[C/T]GATTTAATAGAAATA	84708
rs373058751	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53469304	CAACGAGAACAAAGA[C/T]ACAGCGTACCAGAAT	84708
rs373064720	snp	A/C	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53551656	AGAGATGCAACCCCC[A/C]TGGAAGCATGCCAAC	84708
rs373064882	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53564870	AGTTCCCTTTCCTAA[C/T]CAAAGAAAGGGGTGA	84708
rs373088390	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53531444	AATAATCTTGAAATT[C/T]GATGGCTCAGCCATT	84708
rs373094002	snp	C/T	0.00358779	0.0422022	intron-variant	LNX1	GRCh38.p7	4:53493062	GAAACCTCCGCCTCC[C/T]GAGTTCAAGCAGTTC	84708
rs373128701	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53622822	ACCAGAAAGATTGCA[C/T]ATCATTGTCTGCCAC	84708
rs373152119	in-del	-/GG			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53601327	CTTCCAGTTGTGGCT[-/GG]GTCCCCCTGAAGTGG	84708
rs373155498	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53556735	CAGAACAAATGATCA[C/T]TTCCAAGAACCTAGC	84708
rs373157133	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53466706	TCCCGCACCTGGCTC[A/G]GAGGGTCCTATGCCC	84708
rs373173517	in-del	-/G	0.0490535	0.14873	intron-variant	LNX1	GRCh38.p7	4:53491805	TACTTTTTTTTGTTT[-/G]TTTGTTTTTTGAGAA	84708
rs373186997	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53475088	TACTTCCAGCAAAAG[C/T]AGAGAAGTGCCATGC	84708
rs373189871	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53515374	AATTACAGCATTGGG[A/G]ATTGTGGGATTCACT	84708
rs373190732	snp	G/T			upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53592406	ACCAGAGCAGGCAGC[G/T]GGGAGGTATCCCAGG	84708
rs373201232	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53463238	CTATTTTCTAACCTC[C/T]TGATACTGGAGAGAA	84708
rs373209404	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53469634	GAAGAATCAAATAGA[C/T]GCAATAAAAAATGAC	84708
rs373215777	snp	A/T	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53567339	ACTCAGGATTAAGAA[A/T]CTCACTCAAAACCAC	84708
rs373231101	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53650761	CTTAAAGGATTCCAC[C/T]CTCATGGTTCCAGAG	84708
rs373232050	snp	G/T	1.71587e-05	0.002929	missense, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573885	GGCAGATGTGGCAGA[G/T]GAGGTCATCATCCAC	84708
rs373241346	snp	A/G	0.000153988	0.00877328	synonymous-codon, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508191	TGAGCGCCTCTTCCT[A/G]TCTTTGGTCAGGCCG	84708
rs373349111	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53634542	AGCCACCGCCCCCAG[C/G]CTCAGCTCGGTTTTC	84708
rs373369251	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53517794	GGAAAAAAGTTATGA[A/G]CATTTTTGCGTAGTC	84708
rs373378100	snp	C/T	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53478497	TTTGAAAATAGTCAC[C/T]TAACAAGCTACTAAT	84708
rs373390915	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53579505	CTAAAACCTGTATAG[A/T]AGCTTCTCTGCCTAA	84708
rs373404788	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53643295	AGCTGGGACCACAGA[A/C]GCATGCCACCATGCC	84708
rs373407136	in-del	-/A			intron-variant	LNX1	GRCh38.p7	4:53583561	ATACAGAAAAAAAAA[-/A]ACCCTTTTAAATGGT	84708
rs373413810	in-del	-/T			intron-variant	LNX1	GRCh38.p7	4:53626796	TTCAGAAAAGAGCTT[-/T]ATAATCATAAAAACC	84708
rs373435602	snp	C/T	0.000153988	0.00877328	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508205	TATCTTTGGTCAGGC[C/T]GTAGTGGGAGGCACC	84708
rs373438400	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53632703	TTTTAAACTATGCCA[C/T]GGGGAACCATATCAG	84708
rs373440060	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53512456	ACACTACCCTTTCCT[C/T]TTTCTCCAGTCTTCC	84708
rs373442330	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53649726	GGCATCTCCTCTGTG[C/T]CCACCCAGTCTGGGC	84708
rs373452550	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53495627	AGCTCACTGCAACCT[C/T]CGCCTCCCAGTTTCA	84708
rs373486046	snp	A/C			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519656	TGTGTCTGTCAAGGT[A/C]TCTGACACACACACA	84708
rs373491018	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53569067	AGGAAGAATCAATAT[C/T]GTGAAAATGGCCATA	84708
rs373498081	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53581806	AGCCAAACCATATCA[C/T]GCATCTTGTTTTTGA	84708
rs373504403	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53549084	TGGGTTTAATACCTA[C/T]GTGATGAAATAATAT	84708
rs373516823	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53615034	CTTTTCCTTCAAAAC[A/G]TTGACCCTAGTTTTG	84708
rs373521781	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53543152	AGAAACGAGCCACCA[C/T]GTCTGTCCTGTGTGC	84708
rs373568452	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53573171	ATGATGTCGTTGATA[A/T]GAAGCACTTAGAGCA	84708
rs373568944	snp	A/C/T	4.58958e-05	0.00479018	synonymous-codon, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573694	CCTGAATGGGCAGGT[A/C/T]ACCAGTAGCTTGTTG	84708
rs373582961	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53545848	GGTCTTACTCTGTCG[C/T]CCAGGCTGGAGTACA	84708
rs373615974	snp	A/G	0.0158469	0.0875917	intron-variant	LNX1	GRCh38.p7	4:53471562	AACAGGCAACCTACA[A/G]AATGGGAGAACATTT	84708
rs373622830	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53620698	TACCCCATGAATATA[C/T]AAAAATAAAAATAAT	84708
rs373637202	snp	C/G	8.23811e-05	0.00641746	missense	LNX1	GRCh38.p7	4:53478614	TCCGGGCTCAACACT[C/G]ATGACATAGATAGGC	84708
rs373670121	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53502126	GACTAAAGGATATAA[C/T]AATAATTATTAACTG	84708
rs373672079	snp	C/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53599914	CCACAGTCAGGGCTG[C/G]CTGGCATTGCACCTT	84708
rs373688855	snp	C/G			upstream-variant-2KB	LNX1	GRCh38.p7	4:53653012	TAAGGATTTCTTCTG[C/G]TCATTCTTCAGCATC	84708
rs373693978	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53570987	AGCAGAGATCGCGCC[A/G]CTGCACTCCAACCTG	84708
rs373699885	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53618673	AGTGCTGGCCAATAG[A/G]ATGACAATGCAAGCC	84708
rs373702906	in-del	-/A			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53599220	ACAGGATGAGATAAA[-/A]GATTGGCACAAGACA	84708
rs373707026	snp	A/G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53639530	TCTTGAAACAGAAAC[A/G/T]TACATTAAACAAGGT	84708
rs373739652	snp	C/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519670	TATCTGACACACACA[C/G]ACATGCGCGCACATG	84708
rs373743823	snp	A/C			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53506426	TTATATTGGGGAAAA[A/C]ATATGGGATCTAAGA	84708
rs373800950	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53529885	TTCTCAAAAAGCTTC[C/T]CTATTCCAAGACATG	84708
rs373802626	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53564929	CCCACCCGAATACTG[C/T]GCTTTTCCGACGGGC	84708
rs373808158	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53510901	AAAAGAAACTGGCAC[C/T]TTTCTCTGCTGCCCC	84708
rs373900628	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53612734	TAGAGATGGGGTCTC[A/G]CTATATTGGGTATGG	84708
rs373923397	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53528118	GTTGTTGCCTAATCC[G/T]TTGTGTCCGCTCAGC	84708
rs373938655	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53570652	ACATGTACCCTAAAA[C/T]TTAAAGTATAATAAT	84708
rs373943523	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53606267	TTATCACTGACCCCA[C/T]AGAAATATAAAAAAC	84708
rs373949008	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53635953	GGGCTGATACGGCCA[A/G]TGATGGGGAATTAGA	84708
rs373950311	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53584910	TATATCACATTTGCT[C/T]ACTCAAAACATGACA	84708
rs373953710	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53641129	TGAACACTGGAATGT[G/T]GCATGGTTTTTTGGC	84708
rs373982058	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53583341	GGGTTGGAAGTTTGG[A/G]GTGATGTGTCTGTGT	84708
rs374012426	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53570388	ATGAAATTGGAAACC[A/G]TCATTCTCAGTAAAC	84708
rs374056118	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53542073	TACCTTGCACTCAGG[A/G]GGATGTCAGAAGACT	84708
rs374071943	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53527089	TAGAAGAACAAAACC[C/T]GACCCAAGCTTGTGT	84708
rs374104028	in-del	G/TC			intron-variant	LNX1	GRCh38.p7	4:53562468	AGAGCTCTCTAGTCT[G/TC]AAGACAATCAATGAT	84708
rs374152096	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53582095	TTAATTTTAGAAACC[G/T]AAGAATATCAAAACT	84708
rs374160510	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53626153	AAAGGCCACATGTCA[C/T]ATGATTCCATTTAAA	84708
rs374169191	snp	C/T			intron-variant, utr-variant-3-prime	LNX1, LOC101928879	GRCh38.p7	4:53577468	ATTGGACCAGATTTT[C/T]GTTTTTCAAACTGTG	84708
rs374178802	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53617381	AACCTGTGTTAGCAA[C/T]TAGGATAATATCCAG	84708
rs374188521	in-del	G/TT			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53593681	ATGGGCTTTTTTTTT[G/TT]GGCCATTAGGGCTGT	84708
rs374203553	snp	A/C	0.00318978	0.0398085	intron-variant	LNX1	GRCh38.p7	4:53613013	TTGTAAAACAAAAGC[A/C]CCTGTGTGTGTATGT	84708
rs374206326	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53641842	AGGATTTATTCATAT[C/T]GTAGGTATCAACAGT	84708
rs374210186	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53633595	CATTTTTGTAAACAA[A/G]ACTCAGGGGGCTGGT	84708
rs374210959	snp	A/T	0.000237859	0.0109029	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461063	AAAAAAAACAAAACA[A/T]GATATGATTAGTATT	84708
rs374241693	snp	A/G			utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460508	CAACGTTTCTCAGCA[A/G]TGCATTTTAAAAAAT	84708
rs374250370	snp	G/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53521116	TAGAATAACTGGAAA[G/T]GGTGGGTTTCATGGT	84708
rs374265224	in-del	-/G			intron-variant	LNX1	GRCh38.p7	4:53563879	AAAATGTCAAGGGGG[-/G]TGGGAGGCGAAGGAA	84708
rs374272980	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53637266	ACTTTCTTCACAGCT[A/G]TAGTTCTCAAACTCT	84708
rs374277612	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53633111	AATCCATCAAGTTAT[A/G]TGGACTCTATGATCC	84708
rs374278317	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53647038	AGGATGGAAAGGTTC[C/T]CCATGCTCCATTTTT	84708
rs374284310	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53470325	CAATAAATTAGGTAT[C/T]GATGGGACGTATCTC	84708
rs374285786	snp	A/G	1.64735e-05	0.00286993	missense	LNX1	GRCh38.p7	4:53496178	GCTCATCCACCTTGC[A/G]CACCAGTTTTATTCC	84708
rs374299857	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53606495	AACAAACAAAAAAAA[A/C]ACAGAACAAGACAGA	84708
rs374306344	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53638297	TTTAATAATGCAGAA[C/T]AGTCAATTCTAGTTA	84708
rs374355140	snp	A/C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53502993	TGGAGTGCAGTGGTG[A/C/T]GATCTCGGCTCACTG	84708
rs374358778	in-del	-/ATAA			utr-variant-3-prime, downstream-variant-500B	LNX1, FIP1L1	GRCh38.p7	4:53460360	CGGTGATGGTAACAA[-/ATAA]CATGGTATTTGAAAG	84708
rs374372599	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53471867	GATGTGGAGAAATAG[A/G]AACACTTTTACACTG	84708
rs374412765	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53549385	ATTTGGAATTTGCCA[A/G]AGCTATATTCCTCAG	84708
rs374413015	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53570414	TAAACTATCACAAGA[A/C]CAAAAAACCAAATAC	84708
rs374415255	in-del	-/G			intron-variant	LNX1	GRCh38.p7	4:53555019	GAAAGGAAAATCCAG[-/G]AGGGTCTGTGCATCT	84708
rs374421615	snp	C/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53513289	TTATGGATGTGGTCT[C/G]ATTTAAGCCTCCCAC	84708
rs374434280	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53546052	CCTCAAGTGATCCAC[C/T]CACCTCAGCCTCCCA	84708
rs374444269	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53571173	TACAGGCTTGGGCCA[C/G]CATGCCCAGCTAATT	84708
rs374448115	snp	A/C	1.64868e-05	0.00287109	missense, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498688	CGTCTCTGGCGATCA[A/C]CCCATCACGATAAAT	84708
rs374449561	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53544206	TCTCTCTCTCTCTCT[C/T]TTTTTTTTGAGACAG	84708
rs374452844	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53505230	TTTATAAATGTTTTT[A/G]TAATAAATATGCAAA	84708
rs374458968	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53635447	TTTCATTTAGATTGA[C/T]GTTCTTTTTCCTCAA	84708
rs374477815	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53481406	TTCAAAGTGAATAAA[A/G]TAAGTCCTCAAACAA	84708
rs374510129	snp	A/G			intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53462511	AGATATGGCTATTTT[A/G]TTTATATACCGTACC	84708
rs374511030	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53610734	AAAAAAAAAAAAAAA[A/G]AAATAAACCAAATCT	84708
rs374529742	snp	C/T			nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53604622	GGGGGATATCTGATA[C/T]CTGGAATATTCTTAG	84708
rs374558011	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53564145	GCTGTTTTCCAAAAG[G/T]GCATCTCATTATGAG	84708
rs374572088	snp	C/T	0.00358779	0.0422022	intron-variant	LNX1	GRCh38.p7	4:53554253	CCTATATGTAAGTCC[C/T]CAGTAAAACCCAGTG	84708
rs374587228	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53580728	TATATAAACAGAAGA[C/T]AGTCTTCAGTGGCTA	84708
rs374591085	snp	A/G	4.94784e-05	0.00497361	synonymous-codon	LNX1	GRCh38.p7	4:53476953	GACCTCTGTCAGTTC[A/G]ACCCCATCCACATTC	84708
rs374629146	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53491156	GCTTATTGCGAAGTA[C/T]AGTTGGCAAACATTA	84708
rs374694215	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53622473	ATTGGCGTGGCGAGA[A/C]CACAGCTCCCCTTGT	84708
rs374696140	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53471243	CAAGCAATGGGGAAA[C/G]GATTCCCTATTTAAT	84708
rs374702866	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53531888	CCTGGCAATATATTT[A/C]TTTCTCTCTCTAGAG	84708
rs374713188	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53569658	AAAAGACAAAATTGA[C/G]AAATGGGATCTAATT	84708
rs374719559	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53493836	CTGGATCTTGCCCTT[C/T]TCTTTTCAGCTCTCC	84708
rs374745548	in-del	-/T	0	0	intron-variant	LNX1	GRCh38.p7	4:53541746	CTCAGTCTGAGTCAT[-/T]AAAAAAAAGTAGGCC	84708
rs374765760	snp	A/G	9.9126e-05	0.0070394	stop-lost, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460909	CCCATCATTGATTCT[A/G]TAAAAAAGTGCCAGG	84708
rs374766866	in-del	-/C			intron-variant	LNX1	GRCh38.p7	4:53535425	ATCAAGAATAGCAAA[-/C]TTTATTTCACTCTGC	84708
rs374823159	snp	A/C	3.5076e-05	0.00418769	synonymous-codon, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573985	TTCAGGATCGTTGGC[A/C]GACTCTGGCTGGTTC	84708
rs374842893	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53485917	CTGTCATTCCAGCAA[A/G]CAAGGAATAGCTTAC	84708
rs374871759	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53633776	GAAGAGAGCTGATTG[C/T]CACAGTCAGGCACTA	84708
rs374924313	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53551540	CCCTCAAGTGAGCAC[A/G]TACACAACTTCAGTA	84708
rs374936447	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53505891	AAGGAGAGTGGGAGC[A/G]CAGGCTGGATAATGG	84708
rs374937759	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53522227	TGTCCAATCTGGCTT[C/T]CCACCTGGAGTGGCC	84708
rs374945491	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53583975	AACAACAACAACAAC[A/G]ACAAATGAAGGCAGA	84708
rs374955711	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53532661	TCCCTATGTGACCAT[A/T]TGGAGAGGAAGTTCC	84708
rs375009575	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53554930	ATGCCAAATTTGAAT[C/T]CATGTACTGGATTAG	84708
rs375015456	in-del	-/AG			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53522530	CATATTGACACAGAG[-/AG]TTGCATGGATGTTGG	84708
rs375024759	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53609275	GAACCTAAACTAAAA[A/G]TAAAAAAAAAAGGAA	84708
rs375030364	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53469319	CACAGCGTACCAGAA[A/T]CTCTGGGACACATTC	84708
rs375036382	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53535453	TGCTTACCTGCAAGG[C/G]TACATGACAAATCAA	84708
rs375039545	in-del	-/A			intron-variant	LNX1	GRCh38.p7	4:53472682	AACAACAACAACAAC[-/A]AACAAAAAAAAAAAA	84708
rs375046591	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53630244	GAATTGGGTATTTAT[A/G]CAGTCGAGCCTATTA	84708
rs375052712	snp	C/T	0.000153988	0.00877328	synonymous-codon, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508071	GTAGGCAGGGTTGTC[C/T]AGGCCAGGCTCGTCT	84708
rs375085449	snp	A/C			intron-variant, downstream-variant-500B	LNX1, LOC101928879	GRCh38.p7	4:53577627	GCTATGTTGACCAGG[A/C]TGGTCTTGAACTCCT	84708
rs375092041	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53474923	AGGCGTGTGCCACCA[C/T]GCTTGGCTAATTTTT	84708
rs375092315	snp	A/G			upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53592812	ATTCCCACAGCCTGG[A/G]CCTCAGCTGGCTGCA	84708
rs375115994	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53484685	TAACACTTCTTCTCA[A/G]GGCTCTCTTGAAACT	84708
rs375148509	in-del	-/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53501309	TTTTTGGGGGTGGGG[-/T]GGACAGGATCTCACT	84708
rs375183422	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53609849	TGCTATATAAATAAA[C/T]CATGTAATTTAGATA	84708
rs375199823	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53488210	TGTCCCAAGGCAACA[C/T]TGGCCATTTTTAGAT	84708
rs375204203	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53607005	CAGTCAACATCATAC[C/T]GAATGGGCATAAACT	84708
rs375252438	snp	A/G	0.00438332	0.0466095	intron-variant	LNX1	GRCh38.p7	4:53633827	AGCCACAAACCAGCT[A/G]TGGGACTTTGGGGAG	84708
rs375255593	in-del	-/GAG	0.00795532	0.062565	intron-variant	LNX1	GRCh38.p7	4:53556164	GTTTCCTTATAAGAA[-/GAG]GAGAAGGCAAAGAGA	84708
rs375261163	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53621192	TCCCCAGGTGACTTG[C/T]ATGCATATTCAAGTT	84708
rs375290421	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53586049	ACCCTATTAGAAAAT[A/G]TATTAATTTCCCTTT	84708
rs375314224	snp	C/T	0.000437904	0.0147905	intron-variant, utr-variant-5-prime	LNX1	GRCh38.p7	4:53558019	TGTCAGCTACAAGGG[C/T]CCAAACCAGCCAAGC	84708
rs375343681	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519677	CACACACACACATGC[A/G]CGCACATGCACACAC	84708
rs375354685	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53495028	AAATGGATGTGGCAA[C/T]AGAAGGCAACTTTTA	84708
rs375377267	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53622611	ATAAAAAACGCCAAA[C/T]CCTCTTATTACAACA	84708
rs375392169	snp	A/T	1.73504e-05	0.00294532	missense, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573854	GGAGTGTCCAGGGGG[A/T]CCAGCAAAGCCTGCA	84708
rs375397368	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53540041	CAATACCAAATCTAG[C/T]GCTATCTGAATAAAA	84708
rs375413499	in-del	-/C			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53601692	CTCATCTGTGCCCCC[-/C]TAGAGGCAGCTGCAC	84708
rs375425269	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53468020	TCCTCAAGAAGAGCA[A/G]CTCCAAGACACATAA	84708
rs375430303	snp	A/C/T	4.97668e-05	0.00498812	synonymous-codon, missense	LNX1	GRCh38.p7	4:53496335	CAGCACCTGGCAGGG[A/C/T]TGCCGCAGGAGACGC	84708
rs375438710	snp	A/C	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53574111	AGAACAAGAAGGCTC[A/C]CCTTTGCTTCCCAGC	84708
rs375481245	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53553986	CGGGAGTAGCCAACC[C/T]GGAGGGTCATTCCTT	84708
rs375509134	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53565582	TGGAAACTCTAAAAA[G/T]CAGAGCGCCTCTCCT	84708
rs375511100	snp	C/T	3.4071e-05	0.00412727	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461600	TACAAGCACCTGAAA[C/T]AGAATGTAATCAGTG	84708
rs375522456	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53635043	CTATGTTGCCCAGGC[C/T]GGTCTCAAACTTCTG	84708
rs375529108	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53606618	CATTCTATTTGGTAT[C/T]ATCCTGATATCAAAA	84708
rs375611262	snp	C/T			intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53462501	GCCAAAAATCAGATA[C/T]GGCTATTTTGTTTAT	84708
rs375614056	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53514660	ACAAGATTTGGGTGA[A/G]GACAGTCAAACCATA	84708
rs375642795	snp	A/C	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53582152	ACTACTTTTTTGGAT[A/C]TTGATATTTTCCTTT	84708
rs375678070	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53608495	GTGGAGAAAAGTAAA[C/T]GCTTATACACTGCTG	84708
rs375690901	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53639767	TCAGGTGTAGTGGCT[C/T]ATGCCTGTAATCCCA	84708
rs375692745	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53506984	AAAGAGTAAGGAGAG[C/T]GAATATATATATTGC	84708
rs375693589	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53501731	AGCTAACTGTAGGTT[A/G]CTGAAGCAATGAGGC	84708
rs375704378	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53565286	GTGGTTCTCCCAGTA[C/T]GCAGCTGGAGATCTG	84708
rs375713918	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53580238	GTGCCACCGTTACCC[C/T]AGGAGCTCTTTAGAA	84708
rs375726632	snp	A/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53594228	ACCAGGAAATCCATC[A/G]CCCCTGGGTGCACAC	84708
rs375744341	snp	G/T	0.00835141	0.0640778	intron-variant	LNX1	GRCh38.p7	4:53525754	TGCTATGGTAGGCAA[G/T]CCTGTTAATCTGTGG	84708
rs375751037	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53553971	CCAAGCTAAGGAATC[C/T]GGGAGTAGCCAACCC	84708
rs375765646	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53562981	TTTGGGAGGCCGAGA[C/T]GGATCACGAGGTCAG	84708
rs375777129	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53628417	TAATCATCAGAGAAA[C/T]GCAAATTAAAACCAT	84708
rs375798410	snp	C/G/T	0.000798403	0.0199641	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53601107	AGGGAGGGAGGGAGG[C/G/T]GGGGAGGGAAGGAAA	84708
rs375851345	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53528132	CTTTGTGTCCGCTCA[A/G]CGTATTTTCCCTTTG	84708
rs375867590	snp	A/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53598938	ACTTAGAGTCAATAA[A/G]GAAGCAGAGCTAAGG	84708
rs375976726	snp	C/G/T	4.94599e-05	0.00497272	intron-variant, synonymous-codon	LNX1	GRCh38.p7	4:53557945	GAGCCAAGGCAAGAC[C/G/T]AGCAACAGAAGCGCC	84708
rs375985925	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53514464	GGAGGAGCAAAGTGA[C/T]GTCTCATATGGCGGC	84708
rs376017636	snp	A/G	1.68035e-05	0.00289853	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508045	GGCTGCCCGTCCTCT[A/G]CCGAGGACACGTAGG	84708
rs376024121	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53623052	TTAACTTAGCTTGGG[A/G]CTGGAAGAGATTTCA	84708
rs376026498	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53644793	TATATCTGGAAGGTC[A/G]TTATTACCAACCCAG	84708
rs376036397	snp	A/G	3.3644e-05	0.00410132	synonymous-codon	LNX1	GRCh38.p7	4:53481723	TAGAGGCCTCACCTT[A/G]GGAGTGTTGCTCCTC	84708
rs376044170	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53633407	ATTATTGCTTCTTCC[A/C]AGGATTTCTTCATCT	84708
rs376066893	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53642694	TTTTGGAGAGATCCC[G/T]TGCTCTACTCACCAA	84708
rs376073013	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53555829	TTTTATAGATTGCTT[A/G]TGTCCGTTCAGTTAT	84708
rs376073033	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53526458	ATGCCTACTTTTTGG[A/G]AGAAATTTTAAAGCC	84708
rs376108788	snp	A/G			intron-variant, synonymous-codon	LNX1, LOC101928879	GRCh38.p7	4:53576324	GCTGCGGTACAGCGT[A/G]GCCCTGGTCCTAAAG	84708
rs376148136	snp	A/C			upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53593258	GGAGGGGAGGGAGAG[A/C]CCGCCAACCTGATGA	84708
rs376158214	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53542696	TAATTTAGAAGGCAA[C/T]ACAATTTCGGAATGA	84708
rs376160229	in-del	-/AAC			intron-variant	LNX1	GRCh38.p7	4:53541238	TGAGTGGGTGGAGGT[-/AAC]AACCAAGTTAGGATA	84708
rs376187802	snp	C/T	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53564953	GACGGGCTTAAAAAA[C/T]GGCGCACCACGAGAT	84708
rs376230540	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53533613	CTGTGTTGATCAGAC[G/T]GGTCTCAAACTCCTG	84708
rs376231830	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53527082	AAAAAACTAGAAGAA[A/C]AAAACCTGACCCAAG	84708
rs376232396	in-del	-/AAA			upstream-variant-2KB	LNX1	GRCh38.p7	4:53654299	ATCACATGAAATAAA[-/AAA]CCAAAATGTTGGAAA	84708
rs376233547	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53564456	GGAGGAGTGGCTGGG[G/T]TTTCACTTTCTCCCC	84708
rs376239541	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507869	TGGGTTCCTGCCAAA[A/G]CTACCAGAACGATTT	84708
rs376247079	snp	C/T	0.0154538	0.0865337	intron-variant	LNX1	GRCh38.p7	4:53534667	TAATAATTCTAGGCC[C/T]TGTATTTTGGTCACT	84708
rs376252360	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507167	CTTTAGCTACATACG[C/T]GAGAAGTAGGCTAAT	84708
rs376258638	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53495605	TAGAGTGCAGTGGCA[C/T]GATCTCAGCTCACTG	84708
rs376260848	snp	C/G			intron-variant, upstream-variant-2KB	LNX1, LNX1-AS2	GRCh38.p7	4:53591100	CTCTACTTCTCTTTA[C/G]GTTGTTGTTGTTGTT	84708
rs376261273	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53637653	GTGCAACCTTATTTT[A/T]TGTGCCCACCCAGAA	84708
rs376275145	snp	C/T	1.66194e-05	0.00288261	missense, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461496	TGATGAAAAAAGGTT[C/T]GTTTCCATTGTATTC	84708
rs376318327	snp	C/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53509996	AAAACAGAACAATTG[C/G]ATATTGATGAAGTAC	84708
rs376331351	snp	A/G			upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53593202	ATCACTCACACAAAG[A/G]CCCCCCTCTTCACGC	84708
rs376338061	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53464280	GTACAGCCTCCTACT[C/T]TGATTAACCTAGCAT	84708
rs376354595	in-del	-/ATGCCCTG			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53505406	CAGGTGCCCGCCACC[-/ATGCCCTG]GCTAATTTTTGTATT	84708
rs376395880	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53564006	ATGTGTTGAGGCCCA[C/T]GCCTCCCTGATGTGG	84708
rs376403086	snp	A/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53605484	AAATTTCCAGTATAC[A/T]ATACAATATTTGTAA	84708
rs376410324	snp	A/T			intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53574877	TGTTACTGAATTCAT[A/T]GTCTCTAGTCTAGCT	84708
rs376419969	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53535041	GCTGATGGGAGATGT[C/T]TGTCATTTTGCAGGG	84708
rs376420949	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53520778	ACCAGCCTGGCCAAC[A/G]TGGCAAAACCCCATC	84708
rs376428384	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53580120	CCTTTATTACTTTAT[A/G]AAATAGATGATTCTA	84708
rs376440792	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53550865	AGGGGATACTGAAAA[G/T]CCAGACCAGGGCGTA	84708
rs376445499	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53560589	TCTCAGAAGGCTCTT[G/T]AAAGGAAGGTGTCTC	84708
rs376447774	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53627880	TTGGGAGATTTGAAG[A/G]TGAGGGTTTCAATGG	84708
rs376452957	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53614707	TTTGAGATACCTTTG[G/T]TCAGCCTACGCTGTT	84708
rs376462058	snp	A/G	0.00358779	0.0422022	nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53604115	CTGTAGATGGTAGTG[A/G]GATGGAGGGTGATTT	84708
rs376469735	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53531017	AAAAAATACAAAAAA[A/T]TAGCCGGTGTGGTGG	84708
rs376471836	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53615579	AGCTAAAGGCAGCTG[A/G]ATGAAAACCCATAGA	84708
rs376496219	snp	A/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53504685	TCTAGTTTTTGATTT[A/T]AAGTGAGAGACATGT	84708
rs376500430	snp	C/T	0.00458853	0.0476782	missense	LNX1	GRCh38.p7	4:53478601	TGCTTATGACTCCTC[C/T]GGGCTCAACACTGAT	84708
rs376503033	snp	C/T	1.64738e-05	0.00286995	missense	LNX1	GRCh38.p7	4:53496204	ATTCCAAGCTGCTCC[C/T]CGGGGCTACTTTTGT	84708
rs376505399	snp	A/G			intron-variant, downstream-variant-500B, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460219	GGTGGAGCAGCATGA[A/G]TTTTTATACAGTTAC	84708
rs376505445	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53504364	CTAGCTTCCAACTTT[C/T]CTCCTTTAGCTTCTT	84708
rs376512020	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53467771	ATGAATGAAATGAAG[C/T]GAGAAGAGAAGTTTA	84708
rs376548993	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53632741	AGATTTGGAATTATA[C/T]TGGGATCTGTATCCT	84708
rs376580836	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53570626	GTATGTAACTAACCT[C/G]CGTAATGTGCACATG	84708
rs376599477	snp	A/T	8.94799e-05	0.00668819	missense, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53574002	ACTCTGGCTGGTTCA[A/T]GATGGATTGGAGAGC	84708
rs376607910	snp	G/T			intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53559957	CAAGCCACTGCACCT[G/T]GGTCTACTGTTACTA	84708
rs376608578	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53628812	AAAAAGAAATGAAAT[A/C]ATGTCTTTTACAATG	84708
rs376614040	snp	A/G	8.2373e-05	0.00641714	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507365	TGCCCTGGTCGGCAT[A/G]GTTGGCAACTGCACT	84708
rs376614225	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53494808	AGAGCCCAGAACAAA[C/G]TCTATTCTTCCAAGA	84708
rs376614565	snp	C/T	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53492695	GTTGGGGGAGCAAGA[C/T]GCTGAGGTGAGTCAA	84708
rs376671888	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53571005	GCACTCCAACCTGGG[C/T]GACAGAGCCAGACTC	84708
rs376687323	in-del	-/CT			intron-variant	LNX1	GRCh38.p7	4:53475315	AACTTTAAAGTCATA[-/CT]CTCTACTTTCACTCA	84708
rs376687449	snp	A/G	0.0205511	0.0992634	intron-variant	LNX1	GRCh38.p7	4:53545908	TGCCTCGCAGGTTCA[A/G]GCAATTCTCCCGCCT	84708
rs376688975	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53642279	CCATTTCCACTTTTT[A/G]AAGTTCTTGGGATAT	84708
rs376690297	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53630882	CAAATATCAAGAAAC[A/C]ATTGCATCAGCTTTT	84708
rs376695899	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53638642	CTGTAAAAATGGCCC[C/T]GAAGCATAATGCTGA	84708
rs376723296	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53488301	TATTGGTCTAGTTAT[G/T]CCCAGTAGGGCAACC	84708
rs376726400	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53644266	ATTAGATGGTTATGG[G/T]GGCATGCTCCTGTAG	84708
rs376746749	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53563307	AATTTATAAACAAAA[G/T]CTATGACAAGACTCC	84708
rs376756399	snp	A/G/T	0.000235207	0.0108422	intron-variant	LNX1	GRCh38.p7	4:53496421	TGGAACAATCGTGCG[A/G/T]TCAGCTCCACCTGCC	84708
rs376841105	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53589199	GAATCACATTTTGTG[C/G]GTCTGTTGCAGGATG	84708
rs376868367	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53610941	TGCAAAATTATAAAA[C/G]ATCAGAAAGCAGAAA	84708
rs376887211	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53636875	TACAGGGTCATGTTC[C/T]GTAGTTTAAAACATC	84708
rs376899569	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53581732	TCCCCTTGCGTCCCT[C/T]CCACAACATGTGGGG	84708
rs376915352	snp	G/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53582377	GCAAAGAATGTAACC[G/T]AGGGCCAGGTCTCAC	84708
rs376935915	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508530	GTCTACATGAGTAGG[A/G]TTTGAGGCTGGCAAT	84708
rs376984685	in-del	-/G			upstream-variant-2KB	LNX1	GRCh38.p7	4:53653854	CTCTTGTGTCATGGC[-/G]GGTTACCCAGGGCAG	84708
rs377005663	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53523846	AAGCCTCCATTCACA[C/T]TGTCCCACCATCCTC	84708
rs377014314	in-del	-/AAAG			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53601090	AAGAAAGAAAGAAAG[-/AAAG]GGAGGGAGGGAGGGG	84708
rs377026724	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53483092	TTCCCATATGTCATC[A/G]GAGGGACCTGGCAGG	84708
rs377032985	snp	C/T			intron-variant, nc-transcript-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53523077	AGATCAATCAATCCC[C/T]GGCAGTGGGTCTGCT	84708
rs377037461	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53468920	CCCATTGTCAACATT[A/T]GACAGATCAACGACA	84708
rs377045257	snp	C/T	1.64933e-05	0.00287165	synonymous-codon, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498830	TGGAATCAGGTGGTA[C/T]AACCTTGGAAAGACT	84708
rs377045906	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53471721	CATTTATGCAGCCAA[A/C]AGACACATGAAAAAA	84708
rs377046541	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53650543	GGATTGGAATTGGAA[A/G]TATGAATTTATGGTT	84708
rs377050263	snp	A/G	0.000200127	0.0100012	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507486	TGAGGAATAGCGACA[A/G]GAGGAACAGTAGTTA	84708
rs377052699	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53626445	AAGTAGAAATTAGCT[C/T]TCTGCAACCTAGTGT	84708
rs377066324	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53545041	TTCTATTAAAAACTG[A/C]ACCAGCATCTAAGAG	84708
rs377076205	snp	A/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53593744	CTAGAAAAAAATGTA[A/G]TCATAAAAATGAACA	84708
rs377096616	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53467512	CTTCAACAAGTTGAG[A/G]GAGGAAGGCTTCAGA	84708
rs377115410	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53494097	CACCCAAATCTCATC[G/T]TGAATTGTAGCTCCC	84708
rs377126472	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53582093	TGTTAATTTTAGAAA[C/G]CTAAGAATATCAAAA	84708
rs377140535	snp	C/G	0.00953873	0.0683987	intron-variant	LNX1	GRCh38.p7	4:53540963	CCAACATGGTGAAAC[C/G]CTGTCTCTTCTAAAA	84708
rs377165511	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53545844	ACAGGGTCTTACTCT[C/G]TCGCCCAGGCTGGAG	84708
rs377174724	in-del	-/ACAC	0.499872	0.0079862	intron-variant	LNX1	GRCh38.p7	4:53529102	TAAGAGTCCTGACCA[-/ACAC]ACACACACACACACA	84708
rs377199489	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53619606	ACATGTTGTTTAGCT[G/T]TTCATCACTTGATGA	84708
rs377216570	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53644038	ATAATCCCTGCTCCT[C/T]AAAAGCAAAACCCCG	84708
rs377221530	snp	C/G	0.000153988	0.00877328	missense	LNX1	GRCh38.p7	4:53476863	TTCCTGGGGCTCATA[C/G]TCTTTGACTTCCAAA	84708
rs377224217	snp	G/T	0.00716266	0.059414	intron-variant	LNX1	GRCh38.p7	4:53572800	GGGTGTGTGTGTGTG[G/T]GGGTGTGTGTGTGCA	84708
rs377236429	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53463798	GTATGCTGAAGTCTT[A/G]AGCTGCTCAAGAAGC	84708
rs377244943	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53630567	AGTGCCGCCTGGTGT[C/T]CCTAAGTGCAAGAAG	84708
rs377271170	in-del	-/A	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53606734	CAAACTGAATCTAGC[-/A]GCAGATCAAAAAGCT	84708
rs377290371	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53502801	CAATCCTTTGTTGTC[A/G]TTTCAACAATGTTCA	84708
rs377312588	snp	A/G	6.67835e-05	0.00577818	missense	LNX1	GRCh38.p7	4:53481806	AGATGTCAGGGCTCC[A/G]CTGCCGAACCTGGCG	84708
rs377352719	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53528927	CACACATGTCTGGTT[G/T]GTGGGAAGAGGCTAC	84708
rs377357726	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53556990	TGGTTAGGTTCATAA[A/G]GAGGAATACATTTTT	84708
rs377376627	snp	A/C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53645711	CTGCATTATCTTGGC[A/C/T]TCTCACATGACCACC	84708
rs377377111	snp	C/T	0.000137874	0.00830169	synonymous-codon, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573964	GCCACACACTGCACA[C/T]AGGGGTTCAGGATCG	84708
rs377427567	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53471876	AAATAGAAACACTTT[C/T]ACACTGTTGGTGGGA	84708
rs377435105	snp	A/C	9.91342e-05	0.00703969	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508217	GGCCGTAGTGGGAGG[A/C]ACCTTTACAGCTGTA	84708
rs377495221	snp	A/G	0.00517822	0.0506191	intron-variant	LNX1	GRCh38.p7	4:53470270	AATAGATGCAGAAAA[A/G]CCTTTGACAAAATTC	84708
rs377514616	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53564439	CCTGGATGAGGGGAT[A/G]AGGAGGAGTGGCTGG	84708
rs377527843	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53539119	TGGATAAAATCAGAT[C/G]AGCCGTGTAATCACC	84708
rs377530841	snp	C/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53596930	GTATTTTCTTATTCA[C/T]TCGGATTTTTCATTC	84708
rs377536456	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53553142	ACATTACTACAACCC[A/G]AGATCTCAGAACTCA	84708
rs377557023	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53486559	TGGTTCCTGCCCTCC[C/T]GGAATGTTTCCTACT	84708
rs377567091	snp	A/C			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53600058	AAGGCCCCTCTCCCC[A/C]ATACCATATGCTTTT	84708
rs377572315	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53635098	GTCTTCCAAAGTGCT[A/G]GAATAGCACGCATGA	84708
rs377589260	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53490236	TTCTGCATCAAGTCT[A/G]GAATTGCCTATGGAA	84708
rs377595894	in-del	-/GA			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53516926	TCAGCTCCTTGCAGA[-/GA]CTCCCTGACCATCAA	84708
rs377614115	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53619862	TGTTTTCTCCACATC[C/G]TTGCCAGTGCTTGTT	84708
rs377615913	snp	C/T	0.0352966	0.128072	intron-variant	LNX1	GRCh38.p7	4:53637092	TAAGAGCATACAGCA[C/T]AGACAGAAGCAGTTT	84708
rs377641414	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53633178	CATCCCTTGCAAGGA[A/T]ATTGTGATGATCACA	84708
rs377646560	snp	C/T	0.00557542	0.0525036	intron-variant	LNX1	GRCh38.p7	4:53538070	TTACATAGCAATTGG[C/T]TTCAACCAACCATTG	84708
rs377655910	snp	C/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519654	CCTGTGTCTGTCAAG[C/G]TATCTGACACACACA	84708
rs377656288	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53474712	TTGTCTATGCCGGGA[G/T]ATCATGCTTCCTTAC	84708
rs377672068	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53634704	GCCTCACAGTTGAAT[A/G]TAGTCCATTTCTCTC	84708
rs377690373	snp	A/C			intron-variant, downstream-variant-500B	LNX1, FIP1L1	GRCh38.p7	4:53462783	AATTTCTTTTACTGA[A/C]ATGATTGCTTAAAAG	84708
rs377691085	snp	A/G	0.000313387	0.0125138	synonymous-codon, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573979	CAGGGGTTCAGGATC[A/G]TTGGCAGACTCTGGC	84708
rs377730061	snp	A/G	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53491487	CCAGGAACTGTACCA[A/G]CCTAGTTCAGCATGG	84708
rs377745098	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53635093	CCTCAGTCTTCCAAA[A/G]TGCTGGAATAGCACG	84708
rs377749699	in-del	-/GA/GAGAGA/GAGAGAGAGA			intron-variant	LNX1	GRCh38.p7	4:53492506	GCCTCAGAGGGCTCT[-/GA/GAGAGA/GAGAGAGAGA]GAGAGAGAGAGAGAG	84708
rs377766459	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53563537	GGTTAGCTTCAAATT[C/T]TTTTTTTTTTTTTTT	84708
rs386400058	in-del	-/AGA			intron-variant	LNX1	GRCh38.p7	4:53463641	TTTAGGCCTATCGAA[-/AGA]GATTTGGCATAGTAT	84708
rs386400059	in-del	-/CA			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53514663	GATTTGGGTGAGGAC[-/CA]AGTCAAACCATATCA	84708
rs386400060	in-del	-/TCTGACACAC			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519657	TGTCTGTCAAGGTAT[-/TCTGACACAC]CTGACACACACACAC	84708
rs386400061	in-del	-/TT			intron-variant	LNX1	GRCh38.p7	4:53534419	GAGGCAGGAGGGTCT[-/TT]CGAGCCTAGGAGATC	84708
rs386400062	in-del	-/TTC			intron-variant	LNX1	GRCh38.p7	4:53536333	TCTCACTCCACATCT[-/TTC]TCAAGAGGGGACTTT	84708
rs386400063	in-del	-/G			intron-variant	LNX1	GRCh38.p7	4:53547921	AAGAACCTGACAGGG[-/G]ACCTACCAGTTGTGA	84708
rs386400064	in-del	-/AAA			intron-variant	LNX1	GRCh38.p7	4:53554865	CAAAAAAAAAAAAAA[-/AAA]AATCCTGCCTTGCCC	84708
rs386400065	in-del	-/T			intron-variant	LNX1	GRCh38.p7	4:53626795	TTTCAGAAAAGAGCT[-/T]TATAATCATAAAAAC	84708
rs386400066	in-del	-/T			intron-variant	LNX1	GRCh38.p7	4:53634259	AGCTTGGCTTTTTTT[-/T]TTTTTTGAGATGGAG	84708
rs386674431	multinucleotide-polymorphism	AA/CT			intron-variant	LNX1	GRCh38.p7	4:53475801	GTAATTAAGTGAGAC[AA/CT]GTAATTACGTCACTG	84708
rs386674432	multinucleotide-polymorphism	CA/TG			intron-variant	LNX1	GRCh38.p7	4:53493030	GCTGGAGTGCAGTGG[CA/TG]CGATCTTGGCTCACT	84708
rs386674433	multinucleotide-polymorphism	ATTTTTA/GTTTTTT			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53502419	AGTGTACAATAGCAT[ATTTTTA/GTTTTTT]AAAATGTACATATCT	84708
rs386674435	multinucleotide-polymorphism	AT/GG			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53510102	AAAGATGCACCCAAG[AT/GG]AATTAAAAGTGGTGT	84708
rs386674438	multinucleotide-polymorphism	CA/TG			intron-variant	LNX1	GRCh38.p7	4:53563162	AGTGAGCTGAGATCG[CA/TG]CCAGCCTGGGCGACA	84708
rs386674441	multinucleotide-polymorphism	CA/TG			intron-variant	LNX1	GRCh38.p7	4:53637600	CTTGTTTCATTACTA[CA/TG]GAATTTCATCACTTC	84708
rs386674442	multinucleotide-polymorphism	AA/GC			intron-variant	LNX1	GRCh38.p7	4:53649343	TGTCAATCCCACAAG[AA/GC]GACTACTATTACAAT	84708
rs397690444	in-del	-/TGTT	0	0	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53462359	TACAGGCCAAGTGTT[-/TGTT]AACTATGTTATAATT	84708
rs397692963	in-del	-/A			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508949	TGCTATAAAAAAAAA[-/A]TCCAGAAAACTCCAC	84708
rs397699852	in-del	-/TT			intron-variant	LNX1	GRCh38.p7	4:53463409	TGAGTATTTAACTTT[-/TT]ATTGCCGCAGCGAGA	84708
rs397700597	in-del	-/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53514501	AGGGCTTGTGTGGGG[-/G]AACTCTCCTTTATAA	84708
rs397719050	in-del	-/CT			intron-variant	LNX1	GRCh38.p7	4:53475073	CACCCAGCCCAGACT[-/CT]ACTTCCAGCAAAAGT	84708
rs397728162	in-del	-/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53521985	TTCATTAATTTTTTT[-/T]GTAGAGACTATGTTG	84708
rs397729391	in-del	-/ATCA			utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460629	GGGGTATACAAATCA[-/ATCA]TTTTAGTTGTTTTAG	84708
rs397730993	in-del	-/CA			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53514664	ATTTGGGTGAGGACA[-/CA]GTCAAACCATATCAG	84708
rs397736342	in-del	-/ATT			utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460869	ACTTCTTAGCCTATT[-/ATT]TGTGATTTTTCTGTT	84708
rs397740500	in-del	-/AA			intron-variant	LNX1	GRCh38.p7	4:53526115	CTAGAAAAGAAAAAA[-/AA]TATTAAAAAAAGATA	84708
rs397766595	in-del	-/T			intron-variant	LNX1	GRCh38.p7	4:53535113	ATAGCACCAATGTTT[-/T]TCTCTCTGCATCATA	84708
rs397767116	in-del	-/A	0	0	intron-variant	LNX1	GRCh38.p7	4:53552845	AAAAAAAAAAAAAAA[-/A]GACTTAAATATTTAA	84708
rs397773795	in-del	-/T	0	0	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508437	AATTTGAGATTTTTT[-/T]AAAGACGCCCACTGC	84708
rs397774782	in-del	-/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53518798	TGATTATTTGGGGGG[-/G]CAACTGTAACATGGG	84708
rs397805704	in-del	-/A	0	0	intron-variant	LNX1	GRCh38.p7	4:53490145	CATATAAGGAAAAAA[-/A]CAATTACACATATGC	84708
rs397828368	in-del	-/A			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53515530	CCACCAAAAAAAAAA[-/A]TGACAAGAAGACCGA	84708
rs397932703	in-del	-/T			intron-variant	LNX1	GRCh38.p7	4:53474784	TCTTCTTTTTTTTTT[-/T]GAGACAGAGTCTCTC	84708
rs397937111	in-del	-/TTTT			intron-variant	LNX1	GRCh38.p7	4:53563552	TTTTTTTTTTTTTTT[-/TTTT]GAGACAGAGTCTCGC	84708
rs397939876	in-del	-/A/AC	1.68587e-05	0.00290329	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461055	ATCTAAAAAAAAAAA[-/A/AC]CAAAACAAGATATGA	84708
rs397956013	in-del	-/TT			intron-variant	LNX1	GRCh38.p7	4:53623221	TTTTTTTTTTTTTTT[-/TT]AGGATGGAGTCTCAC	84708
rs397959137	in-del	-/A			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53517786	TGCACATGGAAAAAA[-/A]GTTATGAGCATTTTT	84708
rs397993369	in-del	-/A	0	0	intron-variant	LNX1	GRCh38.p7	4:53466166	TTTAAGAAAAAAAAA[-/A]TCACATATTATTTGG	84708
rs397993370	in-del	-/AT	0	0	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53506429	TATTGGGGAAAACAT[-/AT]GGGATCTAAGACTCA	84708
rs397993371	in-del	-/T	0	0	intron-variant	LNX1	GRCh38.p7	4:53535114	TAGCACCAATGTTTT[-/T]CTCTCTGCATCATAA	84708
rs397993373	in-del	-/A	0	0	intron-variant	LNX1	GRCh38.p7	4:53548134	TGAAAAAAAAAAAAA[-/A]GTCGGGGGAAATATG	84708
rs397993374	in-del	-/A	0	0	intron-variant	LNX1	GRCh38.p7	4:53583562	ATACAGAAAAAAAAA[-/A]CCCTTTTAAATGGTC	84708
rs397993375	in-del	-/AACAAC	0	0	intron-variant	LNX1	GRCh38.p7	4:53583969	AACAACAACAACAAC[-/AACAAC]GACAAATGAAGGCAG	84708
rs397993377	in-del	-/GAGAGAGA	0	0	intron-variant	LNX1	GRCh38.p7	4:53652055	AGAGAGAGAGAGAGA[-/GAGAGAGA]CAGAGAAAGAGATAG	84708
rs398039859	in-del	-/AAAAAAAAA	0.5	0	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53506873	AAAAAAAAAAAAAAA[-/AAAAAAAAA]AAGAGGAATAATAGT	84708
rs398051167	in-del	-/A/GT	0.5	0	intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53574982	TCCATTAGATATTTC[-/A/GT]TTTTTTTTTTTCTTT	84708
rs398083074	in-del	-/A			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53517785	CTGCACATGGAAAAA[-/A]AGTTATGAGCATTTT	84708
rs398092372	in-del	-/G			intron-variant	LNX1	GRCh38.p7	4:53528687	TGTGGATAAGGGGGG[-/G]ACTACTGTATAGCCT	84708
rs398092373	in-del	-/A			intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53574459	GACAAGAAAAAAAAA[-/A]CAAAAAACAGTTAAC	84708
rs398092374	in-del	-/A			intron-variant	LNX1	GRCh38.p7	4:53631709	GGATATATTTTTTTA[-/A]TGCCCTAGGTGATTC	84708
rs398107307	in-del	-/T			intron-variant	LNX1	GRCh38.p7	4:53541486	ATATATATTTTTTTT[-/T]CTAAAAGAGACTTAG	84708
rs398107308	in-del	-/A			intron-variant	LNX1	GRCh38.p7	4:53561936	CAGAATTAAAAAAAA[-/A]GGAAAAAGGAGAGAA	84708
rs527236683	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53491239	AACATGAAAAAGTAC[C/T]GGTGGTCACCTAAAA	84708
rs527292917	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53650045	TACCCTGAGCAGAGA[C/G]TGAGCAGCCCACATC	84708
rs527306062	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53587035	GCAAACATACACCAT[A/G]CACTAAATATGCCAA	84708
rs527342002	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53593679	ATATGGGCTTTTTTT[C/T]TGGGCCATTAGGGCT	84708
rs527342073	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53549590	GTGATATTAGTATTG[C/T]GCTCACATTTCTTAA	84708
rs527342524	snp	A/C	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53586307	ATTCAGAAAAGGCCA[A/C]GTGACTGTCAAAAGC	84708
rs527369692	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53634534	CAGGTGTGAGCCACC[A/G]CCCCCAGGCTCAGCT	84708
rs527373825	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53539124	AAAATCAGATCAGCC[A/G]TGTAATCACCCTGCT	84708
rs527373883	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53524408	ATCTATCACTTTTAA[C/T]ACTCGCCTCCAAATC	84708
rs527400488	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53640924	TTTCTCAGTCTCGTC[A/G]GCAGTCCTTCCGGGG	84708
rs527405570	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53633572	GCTAGGCAGAGTTAG[A/G]TTGGGTTCATTTTTG	84708
rs527406753	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53589307	GACAAATCTGCCCAC[C/G]TTGTTTGATGACATT	84708
rs527433272	snp	A/G	0.00914312	0.0669923	intron-variant	LNX1	GRCh38.p7	4:53565927	AATGAATGAAATGAA[A/G]CGAGAAGGAAAGTTT	84708
rs527438438	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53557716	AAGTCACAGACAGCT[A/T]AGCATGCCGTTTTAA	84708
rs527474873	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53608554	TGGAAAGCAGTGTGG[A/T]GATTTCTCACAGAAT	84708
rs527478140	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53627312	ACAGGGTGGTCCTCA[G/T]TATGTGTTTATCTTC	84708
rs527508159	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53564979	GAGATTATATCCCCC[A/T]CCTGGCTCGGAGGGT	84708
rs527530147	snp	A/G/T			intron-variant, utr-variant-3-prime	LNX1, LOC101928879	GRCh38.p7	4:53576540	TGTATTTTAGGTTGG[A/G/T]CATTTTCATTCTTCT	84708
rs527548268	snp	G/T	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53622226	GTATGTCATATGCCA[G/T]GAAAAGTGGATTTTG	84708
rs527562904	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53476006	CAAGGCCACTCAAAA[A/G]ATAAAACTGGCTGGA	84708
rs527588345	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53628383	TAGCCAAGAAACATG[C/G]AAAAATGTTCAACAT	84708
rs527661695	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53554965	AGCGTCTGAGCTGGG[A/C]ATGAACTCAGGAACA	84708
rs527670791	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53606014	CAATTCTTATCATTC[C/G]TTGTCTTTATCACAA	84708
rs527710079	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53612737	AGATGGGGTCTCGCT[A/G]TATTGGGTATGGCAG	84708
rs527722083	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53552280	GAGTCCCAAACTAAC[C/T]GTGCATCCACTCAAA	84708
rs527722116	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53524574	AGTAAAATGACAGAT[C/T]AAGAAATGAAAAACA	84708
rs527729079	snp	A/C	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53620233	CTCAAAATGTGGTCA[A/C]CACACCTGCAGAGTT	84708
rs527735062	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53532516	CACAAAACCGTCAGC[A/T]GCAAAATGTTTGCTT	84708
rs527736457	snp	A/C	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53581482	TGAAGAAATTACCCA[A/C]GACTGGGTGATTTAT	84708
rs527789885	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53626081	ATGAATATTGACATA[A/T]GTTGCGACATGGATG	84708
rs527801181	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53538417	TGGGGCTCCCACTAA[C/G]TCCAAGGAAAATTAG	84708
rs527813968	snp	C/T	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53609177	GACTCCCGATGTTTA[C/T]TACCTGGCTGGAAAA	84708
rs527824123	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53480978	CAACAGGATGCCAAG[C/T]CAAAGCTATAGGACT	84708
rs527854585	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53559226	CAGGGCTAAAGAGTT[A/T]AAATACAGAAGACTC	84708
rs527854867	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53552654	ACCAATATGGTGAAA[C/T]CCCATCTCTACTAAA	84708
rs527878604	in-del	-/T	0.00159617	0.0282053	utr-variant-5-prime, upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53591441	GGCAGGCAGCTCTCA[-/T]TTCCTTGTGGGTGAA	84708
rs527883173	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53600470	GAAAGGGCAGGCCCT[C/T]AAAAACACAGATTAT	84708
rs527913693	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53599923	GGGCTGGCTGGCATT[G/T]CACCTTGGGAAGAAC	84708
rs527924169	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53475810	TGAGACAAGTAATTA[C/G]GTCACTGTAAGGCTC	84708
rs527948381	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53464770	TTCAGGAGAACAGAA[G/T]ATTTTAAAGCAATTT	84708
rs527950727	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53606595	ATTAAAGGAGGGACT[A/C]CCTAACTCATTCTAT	84708
rs527961390	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53518694	CACACAGCTGGTAAG[C/T]GGAAGGGCTAGGATT	84708
rs527969219	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53558664	CAGAATAACAAAGAG[A/C]CTGGATAGACATAAA	84708
rs527971978	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53645750	GTTTAGTTTAGGTGA[A/C]GTATGCCACTAGAAA	84708
rs527976506	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53469690	CAGAAATACAAATTA[A/C]CATCAGAGAATACTA	84708
rs527978268	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53650856	GGTAGGCCTCCTCTT[A/G]TCTGTATTCCCTGCA	84708
rs527978638	in-del	-/A	0.00322255	0.0400111	intron-variant	LNX1	GRCh38.p7	4:53467592	AAGTTAAAAACCTTG[-/A]AAAAAAATTAGACAA	84708
rs527980498	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53474938	CGCTTGGCTAATTTT[C/T]TGTATTTTTAGTAGA	84708
rs527981344	snp	A/C	0.0178098	0.0926698	intron-variant	LNX1	GRCh38.p7	4:53469195	AGAAACTCACTCAAA[A/C]CTGCTCAACTACATG	84708
rs527986051	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53613224	GTACACATGAACATA[C/T]GTTTAAATTGATCCC	84708
rs528010791	in-del	-/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53641865	TCAACAGTTCATTCC[-/T]TTTTTTCTGCTTAGT	84708
rs528025689	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53569957	TGCAAATCAAAACCA[C/G]AATGAGATACTATCT	84708
rs528029098	snp	A/G	0.00676609	0.0577691	intron-variant	LNX1	GRCh38.p7	4:53564543	GAATAATTATTCCCC[A/G]GAGATGTCCAGCTCC	84708
rs528030704	snp	C/G	0.00119737	0.0244387	intron-variant, utr-variant-5-prime	LNX1	GRCh38.p7	4:53558146	CCGTAAGAAGATTAT[C/G]CTCTCTGATTCTCAG	84708
rs528045651	snp	A/G	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53471637	AATGAACTCAAACAA[A/G]TTTACAAGAAAAAAA	84708
rs528051645	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53521639	CCAATATATTTAAAA[A/G]AAACAACCTTACTCC	84708
rs528069927	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53610633	GAATGGCGTGAACCC[A/G]GGAGGCAGAGCCTGC	84708
rs528086004	snp	C/G	0.000399281	0.0141238	intron-variant, missense	LNX1, LOC101928879	GRCh38.p7	4:53575791	GTGAGTTTCTTGGGG[C/G]CCCAGCTTCCTCCAG	84708
rs528088637	snp	A/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53527164	ATATTCAGTTTTCTG[A/T]TCTCAGCACCAACAT	84708
rs528101816	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	LNX1	GRCh38.p7	4:53653870	GGTTACCCAGGGCAG[C/G]TGGCATCTGGTCAAA	84708
rs528102593	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53568541	CTACAGCCAATATCA[C/T]ACTGAATGGGCAAAA	84708
rs528106006	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53609875	AGATAGCATTATATA[C/T]AACTATATAGCATAT	84708
rs528128335	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53521258	TTTTTGTGAAGTCTA[C/T]GCAACCCCAGGGGCT	84708
rs528131989	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53529345	GCATAGTTGAGGAGA[C/T]AAGGTACTTCTAATT	84708
rs528141509	snp	C/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53624123	TACTTGTTTCCTCTA[C/G]TCATCACCTACATGC	84708
rs528144117	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53528623	TGTATACAGGGTTCA[A/G]TACTATGGTGGTTTC	84708
rs528153971	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53478307	GGTAACTTGCTCATA[A/G]CTGTAGCAGTTCTCT	84708
rs528155723	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53616392	CTGGGTCAGCAGCAC[A/G]TGATTGGTGGGAAGT	84708
rs528194385	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53623650	TTTTAGCCAATCAAA[C/T]TCTCAATTTGAAGTT	84708
rs528214661	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53485472	CACATTTTCAAGGAC[A/G]AATTTCTCACTGGAT	84708
rs528234175	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53644043	CCCTGCTCCTCAAAA[A/G]CAAAACCCCGTGGGT	84708
rs528250364	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53597339	CTTTTTATGATCTGG[C/T]CCCTGTCTGCCTTCA	84708
rs528260185	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53549881	CCAGCTTTGCCTCTT[A/G]TCCGCCTGACATAGT	84708
rs528270995	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53501669	TTGATAAACAGTGGC[A/G]CCAGTCCCTTTACTG	84708
rs528287509	snp	A/T	0.000399281	0.0141238	nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53604203	TAGAAGACAATTTGT[A/T]TTACTCTTTCCCTGC	84708
rs528302489	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53596689	ACCCAGTTCCACATA[C/T]CAGATTTAAAATGTC	84708
rs528315894	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53488051	GGTTCCATAAAATTA[G/T]AAAGTCACAGACACA	84708
rs528324619	snp	A/G	0.000399281	0.0141238	nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53603710	CACTATTGCGAGGAC[A/G]GTACCTTGGGGATGG	84708
rs528337535	snp	G/T	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53463349	TGATATCAGTGTTCC[G/T]AGTTTTATTTAATTA	84708
rs528353878	in-del	-/AG	0.00676609	0.0577691	intron-variant	LNX1	GRCh38.p7	4:53474790	TTTTTTTTTTGAGAC[-/AG]AGTCTCTCTCTGTCA	84708
rs528372598	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53555897	AAGAGAAAATTTTTA[A/G]GTGGTATAAGGACCT	84708
rs528375680	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53472079	ATAACAAAGACTTGG[A/T]ACCAACCCAAATTTC	84708
rs528390706	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53649913	TGGAACCTCGTAAGC[A/G]CTTTGTATCTGTTGT	84708
rs528392419	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53467606	GAAAAAAAATTAGAC[A/T]AATGGCTAACTACAA	84708
rs528428077	snp	C/G			intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53499782	AACAAATGGAAGAGG[C/G]CTGATTCATGATCAA	84708
rs528440543	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53471972	TACCATTTGACCCAG[C/T]CATCCCATTACTGGG	84708
rs528448838	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53642111	CCTGTGATCCCAGCT[A/G]CTTGGGAGGCTAAGA	84708
rs528464569	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53595206	GGGTGGAACAGGAAT[A/G]ATCATAGCAGATATC	84708
rs528475627	in-del	-/A	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53628224	CCCACAGAATAGGAG[-/A]AAAATATATGCAAAC	84708
rs528489816	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53513910	TTTTCTGTCTGTTGT[C/G]ACTTCTGACTTCCTC	84708
rs528491893	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53594659	GCAGTTGGTTTTACC[A/C]CCCAAGATCAAACCC	84708
rs528511057	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53602111	TAGGGACAGAGTGAG[A/G]AATAGAAACTAGGAT	84708
rs528522709	in-del	-/G	0.00676609	0.0577691	intron-variant	LNX1	GRCh38.p7	4:53623990	CCTCAAAAGAATATA[-/G]GTTTTTGTGATGCTG	84708
rs528523258	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53619906	TTAATTATAACCATC[C/T]CAGTGGGTGTGGCAA	84708
rs528540259	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53520523	CATACTTTGGGGAGG[G/T]GGAGCAGGCAATTTC	84708
rs528549583	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53609001	ATCAGAATACCCAAC[A/T]TCAAACCATACTACA	84708
rs528577379	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53641726	ATTGATCTGCTTTCT[A/G]TAACTAGACTGCTTG	84708
rs528579131	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53466549	CAAGGCGTCGCCTCA[C/T]CCGGGAAGCACAAGG	84708
rs528589633	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53470858	TACAAACAAATGGAA[A/G]AACATTCCATGCTCA	84708
rs528594301	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	LNX1	GRCh38.p7	4:53653071	GCATCTTTGCTAACA[C/T]TTATTAAGTGCTTAC	84708
rs528602525	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53560153	CTTCTTGGATGTCCA[C/T]GACCTCCTATATAGA	84708
rs528615480	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53647339	TCTTTTATTTCTGCA[G/T]AGTATAATATTAATC	84708
rs528630880	snp	A/T	0.00478085	0.0486577	intron-variant	LNX1	GRCh38.p7	4:53493234	GGCCTCCCAAAGTGC[A/T]GGAATTAAAGATGTG	84708
rs528643909	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53484893	GCCCATGTCCTTCAC[A/C]CAAAGTCTGGCCATC	84708
rs528651734	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53491402	TGATTGGCCGGCTAA[C/T]GCCACCTGCCTAATG	84708
rs528660855	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53521117	AGAATAACTGGAAAG[A/G]GTGGGTTTCATGGTG	84708
rs528698153	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53518493	TTCAAATCTCAACTC[A/G]CAAATTAATAGTAAC	84708
rs528702371	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53589069	ATCTGTGAGACTGGA[A/G]GAGACCAAACACCCA	84708
rs528704504	snp	A/G	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53542251	GGGATAAATAAACAA[A/G]GGACAGTTTGCATTT	84708
rs528705804	snp	C/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53492734	TTGGTTCAAGTCACT[C/G]GGTAAATAGAGGTGC	84708
rs528710414	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53499899	GATCATCTAGGCTGG[G/T]GTTTTCAAACTGTAT	84708
rs528726467	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53535131	TCTCTGCATCATAAA[G/T]GTTTAGACTTTTTTA	84708
rs528742990	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53544135	CTGAAATAGACTATC[C/T]AGGTGTTTGAGAGCA	84708
rs528774100	snp	C/T	0	0	intron-variant	LNX1	GRCh38.p7	4:53549153	ACCTTGACATGTACC[C/T]CCCAAATCTAAAATA	84708
rs528779861	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53629352	AAGGCCCCAACCACC[A/G]AGAAACAGACCAGGT	84708
rs528781445	snp	A/C	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53548659	TACCATCCCACCCAG[A/C]AATCCCATTACTGGG	84708
rs528802531	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53642591	GGTCAAATCAATGCT[A/G]CAGAGATAGCTCTGG	84708
rs528804621	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53570227	CACGTATGTTTATTG[C/T]GGCATTATTCACAAT	84708
rs528820296	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53588554	ATGGAATGAATAAGA[A/T]TGATATTTTCTAGTG	84708
rs528846592	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53477647	TTCCACCCAGATGTT[C/T]TGCAGAAAAGAGAAA	84708
rs528849202	snp	G/T	0.040671	0.13668	intron-variant	LNX1	GRCh38.p7	4:53567886	TATGCAAATAAACTA[G/T]AAAATCTAGAAGAAA	84708
rs528855890	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	LNX1	GRCh38.p7	4:53653341	CAGCAATGGCCAAAG[A/G]TTTTACTTAAATAAG	84708
rs528865808	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53629807	ACTTGGATAGAGCCC[A/T]TCTGTTTGGTTTTAT	84708
rs528867557	snp	A/G	0.00795532	0.062565	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53520715	GCCTGTAATCCCAAC[A/G]CTTTGGGAGGCTAAG	84708
rs528901535	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53615539	GCCAACTCCCAGACA[C/T]GAGTGAGGCAATTCT	84708
rs528933841	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53484853	TCCTTCTGAAAAGGG[C/G]CCAAAAAAGAAGTTG	84708
rs528953905	in-del	-/A			intron-variant	LNX1	GRCh38.p7	4:53482526	ATACTACTCAGCCAC[-/A]AAAAAAGAATGAAAA	84708
rs528959642	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53477088	GCAGGGATGCAGAGA[A/G]GGCAAAGGTTTTCTT	84708
rs528959972	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53534995	AGTGTTAACCTGTTG[A/G]GATGAAAATGTTTTT	84708
rs528963627	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53506035	GAAAAGGTCTGATAA[A/G]GCTGCTCATGAATTT	84708
rs528994145	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53484115	AGACACCAAACCGGC[C/T]AGTGTCTTGATCTTT	84708
rs529020381	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53534516	AGCATTGAGGACATG[C/T]TTGTAGGCCCAGCTA	84708
rs529045757	snp	A/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53649346	CAATCCCACAAGGCG[A/T]CTACTATTACAATCT	84708
rs529046056	snp	A/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53502453	TCTCAATTTAAAAAT[A/T]CTTTATTGCTAAAAC	84708
rs529056703	snp	G/T	0	0	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53514780	ACTATAGCATCTCAG[G/T]GTAAACACCATACCA	84708
rs529073524	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53583342	GGTTGGAAGTTTGGG[A/G]TGATGTGTCTGTGTG	84708
rs529083025	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53530836	ATTTGCTTTAAAATG[C/T]TCCAGAAAAAAGGAG	84708
rs529111318	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53611750	ATACGCTACAAATAT[A/G]TGAATGAAAAATATA	84708
rs529113876	in-del	-/CATT	0.00358779	0.0422022	intron-variant	LNX1	GRCh38.p7	4:53615219	GTCGTTGTTGTAAGC[-/CATT]CATTCGCTTTTAGGG	84708
rs529118252	snp	C/T	0.00795532	0.062565	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53514250	AAAGACAATGACTGG[C/T]ATATAGAAGGTGCTC	84708
rs529122011	snp	A/T	0.00318978	0.0398085	intron-variant	LNX1	GRCh38.p7	4:53609792	ATAATATATTATTTA[A/T]ATATAAAATATAAAT	84708
rs529125875	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53467554	CTACGAGCTAAAGGA[C/G]GAAGTTTGAACCAAT	84708
rs529148908	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53521164	GTCAGAACTGACTGC[C/T]TAGTGAGGTTTTCTG	84708
rs529159626	snp	A/G	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53616296	AAATAACTCCTATAT[A/G]CCATACACTTAAAAG	84708
rs529188147	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53471264	CCTATTTAATAAATG[A/G]TGCTGGGAAAACTGG	84708
rs529222101	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	LNX1	GRCh38.p7	4:53653843	TAGCAGTTAGCTCTC[C/T]TGTGTCATGGCGGTT	84708
rs529222263	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53585869	TATGGGTATTTGTTA[C/T]GGCAGCCCTAGAAAT	84708
rs529225370	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53550157	ATTTTGGTGAGTTCA[A/G]TGTAAATGAATGAGG	84708
rs529242738	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53553286	TAAACTGTAGTGCCC[A/G]TACGGATCCCCTGGG	84708
rs529246498	snp	G/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53470822	GAACTACAAACCACT[G/T]CTCAATGAAATAAAA	84708
rs529247689	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53560873	CCATCTGATGTAATC[C/T]TAATTAATACAATCC	84708
rs529298108	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53513197	CACGGTCTCTTGCCT[A/G]CAAATCTATGGCAGC	84708
rs529307286	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53600656	TCTCAAATCACGAGC[A/G]TGTGAAGACACCCCT	84708
rs529308637	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53512605	AGTCCAAAAATGAGA[A/C]TAATTTTTCAACTGT	84708
rs529324564	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53608224	AACTGTGCATCCTAC[A/G]AATGTCTAATATCCA	84708
rs529330175	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53559567	AGTAATAGTGCTTAA[C/T]TCAGAGTGCTAGTAA	84708
rs529333750	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53470396	TCATACTGAATGGGC[A/G]AAAACTGGAAGCATT	84708
rs529337048	in-del	-/ATT	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53464505	AGATGTTTATGGGAG[-/ATT]AATATGGACAATCAG	84708
rs529369944	snp	A/G			intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53558868	CCTACCTGGTCTGTC[A/G]GGGACTGGGCCACAT	84708
rs529378929	snp	C/T	0.00795532	0.062565	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519676	ACACACACACACATG[C/T]GCGCACATGCACACA	84708
rs529387966	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53587425	AGTTTTGAAAAGCCT[C/T]TGATACTTTGGAGGC	84708
rs529390482	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53490902	TCCATTTCTTTTTCA[A/G]CTAGCTTTGCTCCCA	84708
rs529402484	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53491858	GCTGGAGTACAATGG[C/T]GCGATCTTGGCTCAC	84708
rs529408265	snp	C/T	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53651892	AAGTAAAGAAGCTTT[C/T]AATGAAGGCCACTGC	84708
rs529418206	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53613875	TCTAGGTCTTTGAGC[A/G]ATCGCCACACTGTCT	84708
rs529421346	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53499374	ATGTTGTCCAGGCTG[A/G]TCTTGAAATCCTGAG	84708
rs529430714	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53588262	TACATGGTAGAACTG[G/T]GTCTGATACACAGAC	84708
rs529437041	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53475894	CTCCTCAGGAGCAGG[C/T]CCTAAGGAGAGATGA	84708
rs529461594	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53636258	GATGCATGCTTGCCT[C/T]GGTCGAGCAAAAACA	84708
rs529465743	snp	A/C	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53587648	AGATCGTATCCTGGT[A/C]AAGAGAGTGAAAGGA	84708
rs529508524	snp	C/T	3.34818e-05	0.00409143	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498625	CTTGCTGCAGCCCCA[C/T]AGCCACAGTCTCTAC	84708
rs529508889	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53647864	GGAATTATATCGTAT[G/T]TGTCCTTCTGAAACT	84708
rs529517778	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53616676	ATAGTAGTAACAGCA[A/G]CAGCAGTAGCAGCAG	84708
rs529528255	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53586039	TAGCAACTCTACCCT[A/G]TTAGAAAATGTATTA	84708
rs529547710	snp	A/C	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53540681	GCAAAGCTCTGTCTC[A/C]AAAAACAAAAAACAA	84708
rs529586729	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53547636	CAAAGGAAGAAAGTC[A/G]GGAAGGGCTCACAGG	84708
rs529590722	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53610228	AGTTAACATTATCTG[A/T]TCATAATTCAATAAA	84708
rs529600644	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53553946	ACACACCTGCATGTG[A/G]TTCGGAGTTCCAAGC	84708
rs529605951	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53635348	GAGCCAACAAAATTC[C/T]TCTTCCTTTAATTAA	84708
rs529608812	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53557357	AAGGCATGTTTCTTC[A/G]TATCCCATAGGTTTC	84708
rs529619902	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53506663	AGTTCGAGACTAGCA[C/T]GACCAACATGGAGAA	84708
rs529645685	snp	G/T	0.00438332	0.0466095	intron-variant	LNX1	GRCh38.p7	4:53631634	ACTTAAGAAGTCCCT[G/T]ATGTCAGACCACAAC	84708
rs529665051	snp	A/G	0.00119737	0.0244387	intron-variant, downstream-variant-500B	LNX1, FIP1L1	GRCh38.p7	4:53462870	AACCTTGATGTCAGT[A/G]GTAAATTCATTCTTT	84708
rs529682335	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53502463	AAAATACTTTATTGC[A/T]AAAACATGCTGTTTA	84708
rs529698253	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53521693	ATTGTGTTATGCAAA[C/T]GAAGGGGGAAAGGAG	84708
rs529703321	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53510487	CTTGTCCTCAGCTGG[A/G]AGAGTTCAAATTCCT	84708
rs529713430	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53509769	ATGTCTAAAATCAGG[A/T]TGCATGTGTGATTGA	84708
rs529722385	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53556775	CAAAGAGCATCTGCT[A/G]TGTTAGACAAATTGG	84708
rs529743244	snp	A/C	0.00318978	0.0398085	intron-variant	LNX1	GRCh38.p7	4:53468315	TTTGTCACCACCAGG[A/C]CTGCCCTAAAAGAGC	84708
rs529766070	snp	A/G	0.000399281	0.0141238	nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53604647	TCTTAGGCTCAATTC[A/G]TTTGTTTCTTCATTT	84708
rs529778579	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53516116	GCATGATGGTGCATG[C/G]TTGTAGTGTCAGCTA	84708
rs529779811	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53562528	CCTAAATGTTTTGCT[C/G]AAGTATTTATATTTA	84708
rs529790657	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53644222	CCTGGCCAGCATGAT[A/G]AAACTCTGTCTCTAC	84708
rs529794100	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53488478	CTCGCTGTAATAAAG[C/T]TGTGTGTGTGCACAT	84708
rs529829361	snp	C/T			intron-variant, utr-variant-5-prime	LNX1	GRCh38.p7	4:53558222	AGCTTAGGCTGAGAG[C/T]AGGCAAGCTGATGCC	84708
rs529840659	snp	A/G	0.000798403	0.0199641	nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53604734	ATTTGTTTCTCATAT[A/G]ATGAACTAGAAGGTA	84708
rs529863222	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53584810	TGAAACACTTCCACT[A/G]ATGGAGAACTGGTCA	84708
rs529891447	snp	A/G			intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53559674	TTTTCAGAGATGGGG[A/G]TCTTGCTCTGTCACC	84708
rs529928680	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53503955	CCTGGCCAACATGGC[A/G]AAACCCTGTCTCTAC	84708
rs529935627	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53544494	CCACCATGTCCGGCC[A/T]GAGAGGTGCTGATTT	84708
rs529941229	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53619309	ACACTTTCATTATCC[A/C]CCAAAGAAATCCCAT	84708
rs529949512	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53551171	GCAGGAAGGGCATAC[A/G]TAAGGCTGCCCATAA	84708
rs529994978	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53594548	GTGCTCCATTCCCCC[C/G]TCCCATACCATTCTC	84708
rs529998374	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53632127	GCAGACCTAGGGCTG[C/G]ATTATGAGGAGACCT	84708
rs529998609	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53465939	GTCCACAAAGTATAG[A/G]GTTTGTGCATAGTAT	84708
rs530000259	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53639702	CATATCTCATGACTG[C/T]AAACACAGTGGAGAA	84708
rs530027263	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53644077	CTGCACTTACTATGT[G/T]TTGTACTTCATTCTA	84708
rs530058968	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53630638	AACTTCCTTCAGGCA[C/T]GCATCACAGTGCTAT	84708
rs530060366	snp	C/T			intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53499478	CTCATTTCTTATATA[C/T]CTCATATCATGCCCA	84708
rs530073326	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53579447	CCCCCATCTCTTTTT[A/G]GTCCTAATCCCTGCT	84708
rs530099681	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53583431	GCTGCCGCCAAGGTC[A/G]TGGTTAGCTCTGCTT	84708
rs530124899	snp	A/C	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53542466	AAGCCCAGCCATGGG[A/C]AGGTGTTTCAAAGAG	84708
rs530131730	snp	C/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53601522	TGGACCAACACTGTT[C/T]GCGTTCTGGCCACCT	84708
rs530133782	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53549787	TCCTTTTATATTGTT[C/T]GTAGTTTTCCATTAT	84708
rs530136883	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53589776	CTTGTGTGTAAATTA[A/C]CCAACAGACCAACTG	84708
rs530140548	snp	C/G	0.000399281	0.0141238	nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53604855	AAAAGAGGCTGCAGG[C/G]GCAGAAAACTGGAAA	84708
rs530144296	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53555876	CTTTGATTTATGTAC[C/T]TGTAGAAGAGAAAAT	84708
rs530153823	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53637056	ATTACCGCCTCAATT[G/T]TTTCACTCTCCTGTT	84708
rs530163330	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53643378	TGATCTCAAACTCCC[A/G]GGCTCAAGTGATCCT	84708
rs530178746	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53589218	TGTTGCAGGATGAGA[A/G]CCTTAGAGTGGGAAA	84708
rs530188620	snp	G/T	0.00398564	0.0444627	intron-variant	LNX1	GRCh38.p7	4:53570374	TTGTAGGGACATGGA[G/T]GAAATTGGAAACCAT	84708
rs530206743	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53648823	GAACACATTCATGGT[A/G]CAGAATTGCTTTAGT	84708
rs530238703	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53500066	GAGGAGGTTTAAGGC[G/T]GAGAGAAGGGGAGTG	84708
rs530239916	snp	A/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	LNX1, LOC101928879	GRCh38.p7	4:53576504	GAGGCAGGCTCTTCA[A/T]CCAGGTGCTTTTGTA	84708
rs530276239	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53474269	GCTACCATTGTGTTT[G/T]TGTGTATGTGTGTGT	84708
rs530280818	snp	C/T	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53530041	AATAGAAGTTTGATA[C/T]GTTTTATCAAGTAAA	84708
rs530311929	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53646633	GAAATTTGAATTTTT[A/G]TATGAAATCTCCTGA	84708
rs530315984	snp	A/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53602858	CAAATATACCTGAAA[A/G]CATAGAAATTTCAAA	84708
rs530324917	snp	A/C			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53599597	GAATTCTTTCTTGCA[A/C]AAGATCCAAGAACCC	84708
rs530332289	snp	G/T	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53570020	CAGGAAAGAACAGGT[G/T]GTGGAGAGGATGTGG	84708
rs530360022	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53472325	GGGAACATCACACAC[C/T]GGGGACTGTTGTGGG	84708
rs530362420	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53617852	TGCTCTATTATTTGT[C/T]AACCAATAGTCAATG	84708
rs530368113	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53521746	GAAATGCTATTATAT[C/T]AAAATATTTATTGGA	84708
rs530393964	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53487107	CTCATACTGTCAGGG[C/T]GTAACATAGATTTGC	84708
rs530394101	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53478976	ACATTGTCCCAAATT[C/T]TACAGGTTAACTCAG	84708
rs530396933	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53562347	GGGAATTCTCTACAG[C/T]AGACCCATGTGATGG	84708
rs530397543	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53467929	TCTGCAAGATAATAT[C/T]CAGGAGAACTTCCCC	84708
rs530422435	snp	C/G	0.000399281	0.0141238	nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53604444	CCAGTTGGATAAAAA[C/G]CAGAACTGGCAGAGC	84708
rs530442890	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53624290	ACATGTAGTGGAAGG[A/G]ATCTGGTGGGAGATA	84708
rs530456127	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53486556	ACATGGTTCCTGCCC[C/T]CCCGGAATGTTTCCT	84708
rs530457018	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53613477	TAAGCCTAGTATCCA[C/T]ATTTGTTATTTTTCC	84708
rs530461755	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53533283	GAACCAGATTTGCCC[A/G]AGGAGCTTGGTAAAA	84708
rs530488329	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53521240	TCTTTTTGAGTCCTC[A/G]TGTTTTTGTGAAGTC	84708
rs530495719	snp	C/T	0	0	intron-variant	LNX1	GRCh38.p7	4:53556019	TCAGTGGAGTGGTGG[C/T]CCCCAAAAGATGTCT	84708
rs530505559	snp	C/T	0.00358779	0.0422022	intron-variant	LNX1	GRCh38.p7	4:53570299	ACTGGATTAAGAAAA[C/T]GTGGCACATATACAC	84708
rs530507483	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53472156	GGAATACTATGTAGC[C/T]ATAAAAAAGGATGAG	84708
rs530520221	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53649636	GTATTTCATCCTTCC[G/T]GCACACCACTCCCTT	84708
rs530529717	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53496972	GTGATACTGTGTGTG[C/T]GCGGATGGGAATGTG	84708
rs530564356	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53569980	TACTATCTCACACCA[A/G]TTAGAATGGCGATCA	84708
rs530565955	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53477083	GGATTGCAGGGATGC[A/C]GAGAGGGCAAAGGTT	84708
rs530592354	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53632182	GAGGCTGGCCGCTGC[A/G]GTGGCCAGGTCTTTG	84708
rs530600553	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53610757	CCAAATCTTCATTCT[A/G]AGAAATTAGAAGAAG	84708
rs530610814	snp	C/T	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53561859	ATAAGAGAGTAGGTG[C/T]AGCAAACCATCATGA	84708
rs530614926	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53495208	CATATTAATTGATAA[C/T]TATCTCAAAATACGA	84708
rs530633938	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53598212	TGACATACTCTACTT[C/T]AGCAATTATTTTACT	84708
rs530635155	snp	C/T	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53617194	AATAAGACCTAGTAC[C/T]TAGTCTAATAATAAT	84708
rs530640751	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53635210	TGTCACATGGGGTGA[A/G]GATGGGCAGAATGAT	84708
rs530669518	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	LNX1, FIP1L1	GRCh38.p7	4:53462672	ACTTGAAATAAAATG[A/G]GCTTTAGGGTTTGGC	84708
rs530675404	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53638870	AGAGAAAAGGGGACA[C/T]TTATACACTATTGGT	84708
rs530682306	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53631447	AGGAAATGTGACCAA[A/G]TTGGCTGTTCCTTGC	84708
rs530722926	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53556685	GGATCCTGGAGTTAT[A/G]TTCCAATAAGATGGG	84708
rs530727304	snp	A/C	0.00159617	0.0282053	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53503058	GCCTCAGCCTCCCGG[A/C]ATTTGGTCATATCTT	84708
rs530744369	snp	A/C	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53509563	CTTCCAAATTTGCAT[A/C]TACTTTCTGGATTGC	84708
rs530757284	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53543809	AAAGAAGAGAGCAGC[A/T]TATGTCCAAAGAAAC	84708
rs530779287	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53631571	AGTTTAAAAAATCCT[C/T]AAGCCAGTGGTTTTT	84708
rs530816734	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53509104	GAACACTGCCACTCG[A/G]CAAGTCATTGCAGCG	84708
rs530821055	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53609039	AATAACCAAAACAGC[A/G]TGGTACTGGTACAAA	84708
rs530828165	snp	A/C	0.000798403	0.0199641	utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460584	CTTCAGCATATACCA[A/C]ATTTTAAATTTAAAT	84708
rs530856986	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53644081	ACTTACTATGTTTTG[C/T]ACTTCATTCTAGTGA	84708
rs530857471	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53491086	CTACAAAAGCAAAAT[G/T]CCATATGTAGTCAAG	84708
rs530878528	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53514638	ATTAGGGGAGCTACA[A/G]TTCAACACAAGATTT	84708
rs530887152	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53636937	TGTATGCAGACCGCA[A/G]GTTCCCTCCCTCCCT	84708
rs530900472	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53641832	TGATAATTTCAGGAT[C/T]TATTCATATTGTAGG	84708
rs530918736	snp	C/T	0.00676609	0.0577691	intron-variant	LNX1	GRCh38.p7	4:53561315	TCATTGCAACCTCCG[C/T]CTCCCAGGTTCAAAC	84708
rs530937547	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53642173	GCTGCAGTGAGCCAT[A/G]ATCACATTACTGCAC	84708
rs530937994	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53499550	TGCATATATCTCTGC[A/G]TGCAGAGGCCTTCAG	84708
rs530973883	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53486386	CACTTCACCCAGCAT[C/T]CCTCTCTTTTTTCTA	84708
rs530993842	snp	A/G	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53529411	GAAAAACTGGGTAAC[A/G]TGGGTGCTGATTTTT	84708
rs531016214	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53583260	AATAGGGAAGAATTA[A/G]GAGCATTAATGACCT	84708
rs531036114	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53467030	CTTGAGATCTGAGAA[C/T]GGGCAGACTGCCTCC	84708
rs531045935	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53554592	GGCACAGTGGCTCAC[A/G]CCTGTAATCCCAGCA	84708
rs531068078	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53542844	ACCCGGTAAGAACCC[C/G]CCTCTCCCATCAGGA	84708
rs531087893	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53630575	CTGGTGTTCCTAAGT[G/T]CAAGAAGGCTGTGAT	84708
rs531124089	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53637516	ACCTGTCATTTCACA[C/T]GTTATTTACTTTTTC	84708
rs531148626	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53493843	TTGCCCTTCTCTTTT[C/T]AGCTCTCCACTGACT	84708
rs531153081	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53589671	AGTAACTTGCTCAAG[A/G]ATATAAATGAAGGAG	84708
rs531166707	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53476450	GTCTCTGCCCCCTCT[A/G]CCTGTCTGTGGAGCT	84708
rs531178913	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53624193	TTTTATACCTTTCCA[A/G]TCATTAGCCTATTTC	84708
rs531179167	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53537918	TGACCTGAGTGAGTT[A/G]CATCTGTACCTCTCT	84708
rs531185095	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53564437	GTCCTGGATGAGGGG[A/T]TGAGGAGGAGTGGCT	84708
rs531194318	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53535751	TCTATTCCCTGCCTT[C/T]ATGCCATCTCTCTTT	84708
rs531250128	snp	C/G	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53630098	TAAAAAAAGGTGGGG[C/G]GGGCATGCGGGTGGG	84708
rs531251590	snp	C/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53502338	TCCAGACTGCTATAA[C/G]AAAGTGAGTCTTTTG	84708
rs531252081	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53590055	AGTGAGAACCTTAGT[A/G]AGAGACAAGTGGTGG	84708
rs531264379	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53493278	AGCCAGAAAATGCCT[C/T]TTCTAACTCTGGTTT	84708
rs531277404	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53582456	ACATAAGCGAGCCCA[A/G]TCAAGTAATAAAGAG	84708
rs531306421	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53651331	CAGCATTCCTTGGGC[A/C]CCGGACTTGCACCAC	84708
rs531319295	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53646922	CACCCCTTTGCCCGG[A/G]AGTTGAAATGAACCT	84708
rs531336204	snp	C/G/T	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53511522	CCTTTTCAACCAAAG[C/G/T]ACAAGCTTTGGAGGT	84708
rs531368875	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53475103	TAGAGAAGTGCCATG[C/G]CCAAGGGCAAATGAC	84708
rs531376959	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53526864	TCTTAAAATCTTTGA[A/C]TCTCCAGCAGCTGGC	84708
rs531386430	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53465206	TTTGGCTGCCCAGTT[G/T]ACATCTTTAAAAAGT	84708
rs531407147	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53614344	CCCTCCCATGACACA[C/G]CATTTCATCTCACAA	84708
rs531429609	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53552554	AATATTTAGGCTAGG[C/T]GCAGTGGCTCACGCC	84708
rs531444901	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53558426	CCCTCCAGTTTGCTA[C/T]AGCGACACTGTAAGA	84708
rs531448138	in-del	-/A	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53550044	GGCTTTACTGCTGGC[-/A]AAAAAAGAATTTGCT	84708
rs531454268	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53525405	GAGAATCGCTTGAAC[C/T]TGGGAAATGAAGGTT	84708
rs531468380	snp	A/G	0.00795532	0.062565	intron-variant	LNX1	GRCh38.p7	4:53532834	TGAGGGTGAATTCAG[A/G]TTCACCCTTCCCTCA	84708
rs531494586	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53483153	CCATGCTGTTCTCGA[G/T]ATAGTAAGTCTCACG	84708
rs531516686	snp	A/C	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53526353	AATCGTTTTCATAAT[A/C]TTGAATTCTCATGTC	84708
rs531530004	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53588654	GTAAGGATGGAGGGG[G/T]CCTGTGAAGTACACC	84708
rs531583238	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53621279	ATTCCCTGTGCAGTG[C/T]CCTCTGCCTGGGATG	84708
rs531590995	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53579022	TCAGAGCCTTGCTGC[C/T]GAATGGAGAAGAAAT	84708
rs531612898	snp	A/T	0.00716266	0.059414	intron-variant, downstream-variant-500B	LNX1, LOC101928879	GRCh38.p7	4:53577663	CAAGCAATCCTCCCA[A/T]CTTAGCCTCCCAAAG	84708
rs531650337	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53555382	TTCCTCTAAGCACTT[A/C]AAGATCCAGCTTAAA	84708
rs531651324	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53634444	AGACGGGGTTTCACC[A/C]TGTTGGCCAGGCTGG	84708
rs531651920	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53532424	AGGTTGTAGTGAGCC[A/G]AGATAGACTCCATCT	84708
rs531654290	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53530939	GAGGCTTAGGCAGGA[A/G]GTATTGCTTGAGCTC	84708
rs531670885	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53625260	TTGAGCCTCCAAGGA[C/T]ACTATCAATAAAATA	84708
rs531673230	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53553720	ATGCTCTTTGTAGAC[A/C]TCAGGGCTGTCCTAG	84708
rs531677411	snp	A/G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53490191	CCCCTATTATCATTG[A/G/T]CTCTAGAAATGGCTT	84708
rs531726200	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53632024	GGAGCGGCCAAAGCT[A/C]CTGGGTCCGCTGGTT	84708
rs531726475	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53487404	TGAGATATAGGTATA[C/T]GCTTAAGTAAAATGT	84708
rs531754086	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53584706	TTTATTTAGAAGTCA[C/T]AGGATTTTGATCGGT	84708
rs531758143	snp	C/T	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53645110	AACAGAAAGTTTGGC[C/T]TAACTCTATTTTTGC	84708
rs531759676	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53496846	ATTGAATTTTTCTCC[C/T]TGGGTCAACTCATAC	84708
rs531770922	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53625932	TGTACACAAGATGTG[C/T]ACACAAACATTCATA	84708
rs531783513	snp	C/G	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	LNX1	GRCh38.p7	4:53558048	GCTCCTTTAAGCAAA[C/G]CTTGCCATGCCCCCA	84708
rs531804868	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53511101	GTTCTTACAACAGCT[A/G]GGGAGGGTGCAGATT	84708
rs531813108	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53650722	CCGTGTCCCCCCAAG[A/G]ACCTCAACCCTAACT	84708
rs531852107	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53516947	CTGACCATCAATCCA[A/G]AGTGAACTGCTGCCC	84708
rs531856242	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53524386	GTACTACCATTTCAC[A/C]CATAGCATCTATCAC	84708
rs531869626	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53652129	TTTTTTTTTAAATTG[C/T]ATGAGATTCTACCTG	84708
rs531904689	snp	C/T	6.58989e-05	0.00573978	missense	LNX1	GRCh38.p7	4:53478661	GTGATGCTCCCCCTG[C/T]GACGGTCATGCCGAG	84708
rs531914996	snp	C/G	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53469083	ATAACTGACCACATA[C/G]TTGGAAGTAAAGCAC	84708
rs531930882	snp	A/C	0.0170251	0.090679	intron-variant	LNX1	GRCh38.p7	4:53606490	CAAAAAACAAACAAA[A/C]AAAAAACAGAACAAG	84708
rs531939639	snp	A/G			utr-variant-5-prime	LNX1	GRCh38.p7	4:53652442	AGTGGTCCCCTGCAG[A/G]GCAGCATGCATTAGC	84708
rs531940280	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53599023	CAGTTACATGAGACA[A/G]CAGGCCAGATTGTTT	84708
rs531946666	snp	A/G	0.00676609	0.0577691	intron-variant	LNX1	GRCh38.p7	4:53551511	ATGAATCCTCAACTG[A/G]TAAGGAGAAAAAGCC	84708
rs531961734	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53473858	GAGTTGAAAAGGATC[C/T]GAGAACACTAAATAT	84708
rs531972089	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53639794	CCCAGCACTTTGGGA[A/G]GCCGAGGCGGGTGGA	84708
rs532020237	snp	C/T	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53474359	ATAAGTAAAATTTTA[C/T]TGGAACACAGCCTTC	84708
rs532022381	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53629592	AGCTGCTCGAAACCA[C/G]TGGCAAAGCCATTTG	84708
rs532029471	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53468728	TAAACCAACAAAGAT[A/C]AAAAGAGACAAAGAA	84708
rs532030587	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53595828	ACAGCGAAGACCATG[A/C]CTTGTGATTCAGCAG	84708
rs532049430	in-del	-/TT	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53591681	GGTAGGTGGCGTCTC[-/TT]TGTGGACAAATAAAT	84708
rs532074000	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53571744	ACAGCTCACTTCACC[C/T]TCAACTCCCAGGCTC	84708
rs532075274	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53551195	CCCATAACTCTTACC[A/G]CTTTTGGCAGTTTCT	84708
rs532078779	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53481451	AAAACATGCCATTTA[C/T]TTGGCTTAGGCTAGA	84708
rs532088803	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53557402	TAAAAATAACATGGA[C/T]ATATACATTTTATAC	84708
rs532144897	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53504017	GTGCACGCCTGTAAT[A/C]CCAGCTACTTGGGAG	84708
rs532152865	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53464540	TTATAAACTCATAAT[G/T]CTGTGTTCAACTTTT	84708
rs532200635	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53605812	CTATAATCTCTTTAT[C/G]CATCATCTATCAATG	84708
rs532206304	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53517500	AGTAACAATAATACA[A/G]CTTCTATTCATAGAA	84708
rs532227432	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53469025	TCTCCACCCTAAATC[A/T]ACAGAATATACATTC	84708
rs532265974	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53613928	ACATTCCCACCAATG[C/G]GGTGTAAAAGCATTC	84708
rs532272211	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53563658	TCCTGCCTCAGCCTC[C/T]CGAGTAGCTGGGATT	84708
rs532293045	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53641517	GGTGGACCTAACGAC[A/C]ATGCCTCTGTTTCTC	84708
rs532309166	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53466340	AAAATTTAAATGATC[A/G]TAAAAAATATGTTTA	84708
rs532328961	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53632903	TTTCTTACTCCCCTC[C/T]TCCTGATTACACTTC	84708
rs532340849	snp	C/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53558381	CACATTCAGACCCCA[C/T]GGTGTGAATAATTAA	84708
rs532360921	snp	A/G	0.00279162	0.0372561	intron-variant	LNX1	GRCh38.p7	4:53530981	ACCAGCCTGGCCAAC[A/G]TGGTAAAACCCCGAC	84708
rs532362166	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53487195	TTGCAGAGCTGTACA[C/G]TGGAGCACAGGGCAT	84708
rs532379043	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53532095	GACGTTATTTCTAAA[C/T]ACAACTATGCAATGG	84708
rs532397324	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53626963	TTTACTCATCATACA[A/C]CTTTGACAAAATGTA	84708
rs532437969	snp	A/G	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53638877	AGGGGACACTTATAC[A/G]CTATTGGTGGGAAGG	84708
rs532493031	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53543784	ATTCAACCCTGTCAA[C/T]CATGCCAAGAAAGAA	84708
rs532503929	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53502310	CATACCTCTGAGATA[C/T]TGTGGGTTTGGTTCC	84708
rs532513493	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	LNX1, LOC101928879	GRCh38.p7	4:53576666	AAGAATCCTGCCTCT[C/T]CCCTCAGCCCCAACT	84708
rs532522914	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53638138	GTACAGATCTTGTCA[C/T]TGGGCATATTTTGTG	84708
rs532551805	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53583925	TGAAATAGAACTGAC[C/T]CCCTGCAAACAACAA	84708
rs532565031	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53488679	CTGTCTTTACCTATG[C/G]ATTAATTGAAAGGTG	84708
rs532609411	snp	A/C	0.000399281	0.0141238	intron-variant, nc-transcript-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53523000	TCCAGTGGTTCTTAA[A/C]CTTGGCTGAGCAACA	84708
rs532622928	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53612016	TTTATAATATGCAAA[G/T]ATTTGTTATGATTTG	84708
rs532642568	snp	A/G	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53543113	CAATTCTCCTGCCTC[A/G]GCCTCCCGAAGTGTT	84708
rs532673790	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53462456	TGTAGTCCGGGAATT[A/G]GTTTGAAAGGAAATT	84708
rs532676028	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53494286	CATGTAAGACTGGCC[C/T]TTCACCTTCTGCCAT	84708
rs532678589	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53472186	GTTCATGTCCTTTGT[A/G]GGGACATGGATGAAG	84708
rs532681399	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53571086	CTCTGTCACCTAATC[G/T]TGGCTTACTGGCAGC	84708
rs532702843	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53535871	GTATGTCTACATTTG[A/T]TATGACCCCTGATAA	84708
rs532731730	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53612548	ATACAGTCATTAAGA[A/G]TAAATTAACGCTTGT	84708
rs532741401	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53605467	CTAAATATGTTCCCA[C/G]TAAATTTCCAGTATA	84708
rs532819679	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53634393	GGACTACAGGTGCAC[A/G]CTGCCAGACCTGGCT	84708
rs532837752	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53480631	CTGTCTAGACTCCTT[A/G]TTGTAGAGAAACAGG	84708
rs532842975	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53618001	GTGTTTGATTATTTA[C/T]TTTTCTTATTGGTGT	84708
rs532881128	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	LNX1, LOC101928879	GRCh38.p7	4:53577602	TATTATTTTTTAAAG[A/G]TGGGGTCATGCTATG	84708
rs532886529	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53488315	TGCCCAGTAGGGCAA[C/T]CCCACATCAATTTCC	84708
rs532898055	in-del	-/T			intron-variant	LNX1	GRCh38.p7	4:53634253	CTGTCCAGCTTGGCT[-/T]TTTTTTTTTTTTGAG	84708
rs532903283	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53479784	CTCAAACTATAAGAT[A/G]TATTTCCATTTTAGA	84708
rs532916873	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53491271	GCTAGTTTTCAAAGT[A/G]AGAAAAAAAAAAAAA	84708
rs532944821	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53480429	TTGATGACTTAGAAT[A/G]TGACGTATTCTAGTT	84708
rs532951106	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	LNX1	GRCh38.p7	4:53653757	AGATGAAGTCAGCAC[A/G]TGTATTTTCAGTCCT	84708
rs532970919	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53609115	TGCTTCACTCCTACA[A/G]CTATCTGATGCTCAA	84708
rs532973024	snp	A/C	0.00398564	0.0444627	intron-variant	LNX1	GRCh38.p7	4:53609737	ACAATATATAATATA[A/C]TATTATATATTATAT	84708
rs532990150	snp	G/T	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53534292	TCAAGGGCATATGTT[G/T]CTGGGTAGGGGCCCA	84708
rs533003747	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53540509	GACATGGTGAAACCC[C/T]GTCTCTACTGAAAAT	84708
rs533013380	snp	C/T	0.00438332	0.0466095	intron-variant	LNX1	GRCh38.p7	4:53527694	CCCTCACTGGATTGG[C/T]GGTAAAGCTCATACT	84708
rs533039496	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53632117	GGTACCAAGGGCAGA[C/T]CTAGGGCTGCATTAT	84708
rs533057996	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53622806	GGCTGACCCATGTGT[G/T]ACCAGAAAGATTGCA	84708
rs533061791	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53635222	TGAGGATGGGCAGAA[C/T]GATACCATTAGACTC	84708
rs533073838	in-del	-/T	0.00676609	0.0577691	intron-variant	LNX1	GRCh38.p7	4:53623988	TTCCTCAAAAGAATA[-/T]AGGTTTTTGTGATGC	84708
rs533107506	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53547227	GATGGAATCTATTTA[A/C]AGGAGACATTAAGAA	84708
rs533119249	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53484742	AATTAAAGGAACTTT[C/T]AGAGACAACTGCTAG	84708
rs533130837	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53471184	CCCTCAGAAATAATG[C/T]CGCATATCTACAACC	84708
rs533152154	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53602150	GCAGAAACCCAAGGT[A/G]GTGAAAATGAAGTTA	84708
rs533157951	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	LNX1	GRCh38.p7	4:53653152	TCTCCACAGAATCCT[A/G]TAATTATCACTCCCA	84708
rs533198964	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53606649	CCTGGCAGACATACA[A/G]TAAAAAAAGAAAACT	84708
rs533212525	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53533442	CTCCCTCTGTCGCCC[A/C]GGCTGGAGTGCAGCG	84708
rs533226035	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53531758	AAGCCACAATTTCTG[C/T]ACTTCATTTTTCTTG	84708
rs533232508	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53613308	ACCTTGCCAGTTTGA[C/G]GGTTTCTGTTTCACA	84708
rs533237060	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53474995	CTGGTCTTGAACTCC[C/T]GGTCTCAAGTGATCC	84708
rs533240651	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53573298	TATGGAAGATGAAAA[A/G]TTTCTAGAGATGGAT	84708
rs533249414	snp	A/C	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53567860	CCATCAGAGAATACT[A/C]CAAACACCTCTATGC	84708
rs533293343	snp	C/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53574980	ATTCCATTAGATATT[C/T]CGTTTTTTTTTTTTC	84708
rs533297410	in-del	-/AGAT	0.00119737	0.0244387	utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460835	ATATAAAAACTGACA[-/AGAT]AGATAAATATAGTGT	84708
rs533306649	snp	A/G	1.64751e-05	0.00287007	missense	LNX1	GRCh38.p7	4:53476894	GCTTTGAGTACTATC[A/G]AGGATGATGTTCTTT	84708
rs533311994	snp	A/G	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53566045	CCTGAAAGTGATGGG[A/G]AGAATGGAACCAAGT	84708
rs533332281	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53651758	GTGGAATGAAACAAA[A/G]TCTGTGTGTGAATGT	84708
rs533338943	snp	G/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53563992	GGAGGCTTGAGAGCA[G/T]GTGTTGAGGCCCACG	84708
rs533343417	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53497930	TATCTGAGTGTCAGA[C/T]AGAAAATATACGAGC	84708
rs533344385	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53587152	TTCTTCCTCTTACTG[A/G]TCTGAAGTGTGTATC	84708
rs533390861	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53613802	ATAATAGAATGATTT[A/C]TATTCCTTTGGGTAT	84708
rs533398988	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53600604	ATTCCGACTAACAGG[G/T]TCTCAATATAATAAT	84708
rs533407156	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53526126	AAAAATATTAAAAAA[A/G]GATAACATACGCCAC	84708
rs533421466	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53525396	TTGAGGCAGGAGAAT[C/T]GCTTGAACCTGGGAA	84708
rs533429707	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53621188	AAGATCCCCAGGTGA[C/T]TTGTATGCATATTCA	84708
rs533448628	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53641003	GAAAAGGTATTGGAA[A/G]GCTGGCTGCTAATTG	84708
rs533466572	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53620398	CACCAATCTGTGTTT[C/T]AGCAAGCCCTGCAGG	84708
rs533482566	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53532628	GAAATTCTCCTCATG[C/T]CAGTTGGAAAATAAC	84708
rs533533995	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53490474	GAGGCTTCTATCTCC[A/G]TAAGGACTTTCTTCT	84708
rs533562744	in-del	-/G	0.00676609	0.0577691	intron-variant	LNX1	GRCh38.p7	4:53641208	GGGGAAGGGCGGGGT[-/G]GGGGGGGCACCTCCT	84708
rs533577578	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53572221	CGTCTCCCATACCTG[G/T]GCAAAACTTTCAGCA	84708
rs533579764	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53524915	TCTTCTGATTTCACA[G/T]GATCTGGGGGTGCTT	84708
rs533626961	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53627151	CCAGCCTTGGTCTCA[C/T]AGGATAATGGTGGTT	84708
rs533629832	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53620060	TTGTAACGAAACACA[A/T]TGTGGCTTTTGTTAA	84708
rs533630157	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53465854	CAAATTTTAGTTTTC[A/G]CAAATACCTTGGCAA	84708
rs533664339	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53553216	AGAGAGGAGTGATAA[C/T]TTTCAACAGGGAAAG	84708
rs533690460	snp	A/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53559601	GGTGAAATGAGGCAA[A/T]GCCCATAAACAACAA	84708
rs533690728	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53559406	TGGAAAGCAGTAGAA[A/G]GAAGTTAGGTTTGAT	84708
rs533692696	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53552900	GATGACTGACCAGCA[C/T]AATGACAATCCCAGT	84708
rs533716779	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53470425	TTCACTTTGAAAACT[A/G]GCACAAGACAGGGAT	84708
rs533720994	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53640625	AGGAGAACCACAATA[C/T]ATCCATAACCCCCAA	84708
rs533724213	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53474754	TAGAGGAAATGAGCA[A/G]AGTGCAGACTCTACT	84708
rs533736872	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53593185	TTTGATAATTGAGAA[A/G]CATCACTCACACAAA	84708
rs533749358	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519905	CTGGATTCTTGAGAC[A/G]TGGGATTTTTGGTTT	84708
rs533750286	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53647272	AAATGTTTTAGTAAT[A/G]TGCATACACAAACAC	84708
rs533768709	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53572860	TAGCAGAACAAATTG[C/T]TTGGAAGACAAAAGT	84708
rs533776846	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53600191	ACTTGCTGTTTTTTA[C/T]GCTGTCCAATAGAGT	84708
rs533786821	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519710	ACACTCCTTAACAGG[C/T]GTCAGGCTATTCTGA	84708
rs533792854	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53579940	TGAAATTGTTGCCTG[A/G]GTCACAGTTTTCTAG	84708
rs533823985	in-del	-/A	0.00755907	0.0610114	intron-variant	LNX1	GRCh38.p7	4:53626708	ATAAATAGGCAAACC[-/A]AAAAAAAAGAAGGAA	84708
rs533880257	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53651454	AGGAATACATGACAA[A/G]GTGGTATATTGTACA	84708
rs533885159	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53469334	TCTCTGGGACACATT[C/G]AAAGCAGTGTGTAAA	84708
rs533891603	snp	A/T	0.00755907	0.0610114	intron-variant	LNX1	GRCh38.p7	4:53538414	ATTTGGGGCTCCCAC[A/T]AACTCCAAGGAAAAT	84708
rs533921525	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53489559	TCTCATGATTATGTT[C/T]TATAAAAATATATAT	84708
rs533922393	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53619140	AAATGAAAATGTTAG[C/T]ACCACCAAATAACAT	84708
rs533932936	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53598617	CTCAGGACTTAGCCT[G/T]GTATCTGGAAGAAAC	84708
rs533952205	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53562982	TTGGGAGGCCGAGAC[A/G]GATCACGAGGTCAGG	84708
rs533959779	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53605637	TCTGTTTCTCTGTAT[C/T]CATGTTTTTTTTAAA	84708
rs533960318	snp	A/C	0.0023933	0.0345097	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53505404	TACAGGTGCCCGCCA[A/C]CATGCCCTGGCTAAT	84708
rs533997734	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53516426	CCTCCATGCCACATT[A/G]TCAGAGAGACAGAGA	84708
rs534009028	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53607918	TGGCTAGCCAGATGC[A/G]GAAGATTGAAACAGT	84708
rs534014960	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53468452	ATGAGCAAGCTAACC[A/G]GCAAACATCATAATG	84708
rs534045544	snp	G/T	0.00119737	0.0244387	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53518958	GTCATAACGGGGTTG[G/T]CATCTTCAGCCTGGA	84708
rs534049113	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53606905	TCTGATAAAATTCAA[C/T]ATCCCTTCATGTTAA	84708
rs534075180	snp	G/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53470002	TTTATGAGGCCAGCA[G/T]TATCCTGATAACAAA	84708
rs534084047	snp	C/T	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53613503	TTTCCTGATCCTCTC[C/T]GTCCTCCACCCCCCA	84708
rs534120417	snp	A/G	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53564787	GGTCAGTGGGTGCGC[A/G]CACCCTGCGCCAGCC	84708
rs534133400	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53557572	CTTCAGTTCTATTTA[C/T]GGAAGGAAGAGAAGT	84708
rs534149370	snp	C/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53601790	AAGATGGCATCTTCT[C/T]CAGGATAAAGGAATA	84708
rs534159740	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53529676	CCAGAGTGTGAGAGA[G/T]TCAGGAGGAGGTGTA	84708
rs534164484	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53468759	GGCCACTACATAATG[C/G]TAAAGGGATCAATTC	84708
rs534194707	snp	C/T	0.00279162	0.0372561	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53503811	CCTAGATGGCATCTT[C/T]TCCCAATATAAGGCT	84708
rs534207804	snp	A/C	0.00438332	0.0466095	intron-variant	LNX1	GRCh38.p7	4:53544886	AAGACACACAGCCAG[A/C]AATTGGCAGGGCCAG	84708
rs534220633	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53632541	TCATGGCAGGATGAA[C/T]TCTGGGGTGCAATTC	84708
rs534234512	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53650657	TCTTTTCACCGTTCT[A/T]TACTACCGCCCTACA	84708
rs534250484	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53528266	ATAGTTTTGCTTTCC[A/G]CAGTTTCAGTTACCT	84708
rs534256839	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53639407	TGGGTGACAGGATCA[C/T]TTGTACCCCAAACCT	84708
rs534276082	snp	G/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53500593	ATAAAGAATTAAAAT[G/T]ATTTCTAAGTATGTT	84708
rs534279096	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53473901	ATATATCAAAGAAAC[A/G]AATTTCTAGAGTCCC	84708
rs534290969	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53467146	CCTCTGAGACAAAAC[A/T]TCAGAGGAATGATCA	84708
rs534303853	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507796	CCAAGTCAGATTACA[C/T]ACAGTTTTAATGATT	84708
rs534311922	snp	C/G	0.000798403	0.0199641	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53603027	TCTGGGCCTCAGTTC[C/G]TTCATCCCTAAAAAG	84708
rs534312504	in-del	-/C			intron-variant	LNX1	GRCh38.p7	4:53579741	TTGGTGTGCTGTTGT[-/C]CCTGCTAATTCTCCT	84708
rs534334656	snp	C/G			intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498406	AAAATGATATAGAGA[C/G]AGATAAATATTTATA	84708
rs534365869	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53545355	CTCAGCCCCCCAACC[C/T]GGCCCTACTGAATTA	84708
rs534374929	snp	A/G	0.00199481	0.0315187	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53520828	TTAGTTGGGTGTGGT[A/G]GTGAGTGCCTGTAAT	84708
rs534377561	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53601824	AACCACATGCCAGGG[A/G]TCACTGCAGGTCACT	84708
rs534402080	snp	C/T	0.000114748	0.00757369	intron-variant	LNX1	GRCh38.p7	4:53496419	GGTGGAACAATCGTG[C/T]GGTCAGCTCCACCTG	84708
rs534406231	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53560902	CCCTTGGGGCTAAAA[C/T]CCAACCTCAAATGAA	84708
rs534407942	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53584926	ACTCAAAACATGACA[A/C]ACACATCCCCAAATT	84708
rs534419591	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53592286	TGATATAGCCAGGAA[A/G]GAGACGTCAGAGTTA	84708
rs534430199	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53588187	TCTGGGAAGTATTTC[A/T]TTTCCCAGCTGATGA	84708
rs534457311	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53477706	TTTCTATTTTTTTAT[C/T]TTCATCCTGTTTTTT	84708
rs534468322	snp	G/T	0.00914312	0.0669923	intron-variant	LNX1	GRCh38.p7	4:53567935	CATACACTCTCCCAA[G/T]ACTAAACCAGGAAGA	84708
rs534478108	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53535448	CACTCTGCTTACCTG[C/T]AAGGGTACATGACAA	84708
rs534482381	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53611985	AATCTATATAGTGTG[A/G]ACACTAGTTATCATT	84708
rs534519825	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53500604	AAATTATTTCTAAGT[A/G]TGTTAGGGCAAAGTA	84708
rs534531274	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53589250	GGAAGAAATCACAGC[C/T]AGCCAGCAACTCCTA	84708
rs534544304	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53463919	GACTACAAAAAACAC[C/T]AAGGCAGAGCCTCTT	84708
rs534550417	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53554874	AAAAAAAAATCCTGC[C/T]TTGCCCCTGCAGGCA	84708
rs534567059	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53463447	ATGTTAATCTGTTTC[A/T]AAGTCATACCTTGGT	84708
rs534610858	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53648335	GTATCTCATTGTGGT[C/T]TTTGATTTGCTTTTT	84708
rs534611933	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53637147	TGGCAAAAAAAATCT[C/T]ATAAGTATAAGAGGA	84708
rs534673595	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53580875	TCCAAAATGTACCAA[C/T]ATAGTAAATAACACA	84708
rs534713174	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53587266	CGGGAGACAACAAAC[A/G]TTTTCTGTTCCTGAT	84708
rs534731015	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53520256	AGGGACTGAAAGAAC[C/T]GATTCCATTGTTTAG	84708
rs534748854	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53647738	TGCAAAACTGAAACT[C/T]GTCACCCATTAAACA	84708
rs534759312	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53560424	CAACCACTGCTGGTT[A/G]CCTATCAAATATTTA	84708
rs534760178	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53471006	TTTAAAGTTCATATG[A/G]AACCAAAAAAGAGCC	84708
rs534826043	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53582280	TTGTTGCTTCAGCTG[A/C]TTGTTACACTTGACA	84708
rs534830900	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53553328	GAATGAAAATGGGGT[A/G]GCCTCATGAGAATCA	84708
rs534833917	snp	A/G	0.00993419	0.0697739	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461730	GTCCCACTCAAAATT[A/G]TATCATACCTTGGTG	84708
rs534848218	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53477110	GGTTTTCTTTGTTGA[C/T]GGGAGGCTGGGTGCT	84708
rs534852453	snp	C/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53575124	GTAGCTGGGATTACA[C/G]GCGCGCGCCACCATG	84708
rs534870887	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53466484	CACTAGGGAGTGCCA[A/G]ACGGTGCAGGACAGT	84708
rs534891716	in-del	-/TT			utr-variant-3-prime, downstream-variant-500B	LNX1, FIP1L1	GRCh38.p7	4:53460424	AATACAAAAGTAATC[-/TT]TTAATTAGTATCACA	84708
rs534893720	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53549462	AGAAGAGGAGGAGGA[A/G]GTTGAAAGAAACTTA	84708
rs534897328	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53541827	ATAAAAATGTTTAAA[C/T]CCTGCAGTGCTAAAC	84708
rs534954028	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53636549	CTTGAACCATAAAAT[A/G]GAGATGATAATGCCC	84708
rs534956731	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53548888	AGGAACATGGACGGA[A/G]CTGGAGGCTACTATC	84708
rs534976856	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53635662	TTTAATGATTCTATG[A/C]AACTCATGAAAAACA	84708
rs534977008	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53628020	GGATATCGGTTTACA[A/G]CACTCCAACTTGAAG	84708
rs535013065	snp	A/G	0.0002307	0.0107376	synonymous-codon, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498698	GATCACCCCATCACG[A/G]TAAATGTGTTGGATA	84708
rs535021570	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53621873	ACCTTTCATTTCACC[C/T]CCACCGGATTTGTTG	84708
rs535028478	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498169	GAGGGCCGTAAGACT[A/G]TAGGAAATTGACTTT	84708
rs535078431	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53580637	AGGTAGAAATGAAGA[A/C]GTTTTTAAAAACAAA	84708
rs535093140	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53506139	AGCTAAGAGAGTAGG[C/T]TCTGGAACCAGAGGA	84708
rs535094026	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53468400	AACATGCCAAATTGT[A/G]AAGACCATCGAGGCT	84708
rs535108820	snp	C/T			upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53591629	AAAGAGTCAGGAGGC[C/T]CCGCCCACCTGTCAT	84708
rs535120447	snp	A/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53634869	GAGAGACAGGGTCTC[A/T]CTCTGTCACCCAGGC	84708
rs535125213	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53614744	TCACGAGTTCATCTC[C/T]TCCTTGATGTCAACT	84708
rs535126456	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53520093	AAGCTAGTTTTGGAG[A/G]AGCTTTGTGGTTTCA	84708
rs535127429	snp	G/T	0.00398564	0.0444627	intron-variant	LNX1	GRCh38.p7	4:53642080	TAAAAACATCAGCCA[G/T]GTTTGGTGGTACACG	84708
rs535140449	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519762	TAATCTTCACAACAA[C/T]CTCATGAGATGGGCA	84708
rs535177300	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53477014	AGAAGCTATCTTTAG[C/T]GAGAGCACAAACAGG	84708
rs535181097	snp	A/C	0.0372196	0.131242	intron-variant	LNX1	GRCh38.p7	4:53566681	AATGGACTAAATGCT[A/C]CAACTAAAAGACACA	84708
rs535184393	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53608051	CCATTCTGGACACAG[A/G]GTATGGCAAAGATTT	84708
rs535184728	snp	A/G			nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53603850	TATCCAGACTATATC[A/G]GGGCTGTACCAGCAA	84708
rs535198284	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53639695	AGCTGTTCATATCTC[A/G]TGACTGCAAACACAG	84708
rs535209097	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	LNX1	GRCh38.p7	4:53652542	AAGCCAAGGTCCTTT[C/T]GTTCACCTTTAGGGT	84708
rs535216823	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53622468	ACCTGATTGGCGTGG[C/T]GAGACCACAGCTCCC	84708
rs535240000	snp	A/G	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53474853	CTCACTGCAACCTCC[A/G]CCTCCTGGGTTCAAG	84708
rs535242431	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53574241	GAGTGACTGACAGGA[A/C]CTTGGGCAAGCCCCA	84708
rs535245914	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53652096	TGAGAGCTGGAGGCT[A/G]AGTGGGCAGAGGTGA	84708
rs535261149	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53615020	AAAATATATTTTTCC[C/T]TTTCCTTCAAAACAT	84708
rs535261785	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53548830	ATAGATATACCATGG[A/G]ATACTATGCAGCCAT	84708
rs535262639	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53527279	ATTCAAGGTGTAAGC[C/T]ATTTTTCTAAGACAA	84708
rs535271540	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507626	TTTTTTAAGTTTTCT[A/G]CAGTGAAATATGTAC	84708
rs535326310	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53595477	TCTTATGCATGACAA[C/T]GGTTTTCAGCATTGA	84708
rs535329522	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53534573	CTTAAACCCAGGAGT[C/T]TGGGGTTGCAAAGAG	84708
rs535343003	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53533813	GCCCCCACAACCAAG[A/G]ATTATCTGGTCCAAA	84708
rs535357730	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53602193	ATAAGGGGATGGATC[C/G]AAATCTGTGACCTTG	84708
rs535358346	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53642315	ATGAAAGAAGGAATC[C/T]CAAAATAGACCTATA	84708
rs535358360	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53635788	TGCTTTTAATATCAG[A/G]GAGACTGTGCCCAGT	84708
rs535365308	snp	A/G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53554784	TTAAACCCGGGAGGC[A/G/T]GAGGTTGCAGCTAGC	84708
rs535394005	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53560297	CTTTTATTAAAAAAG[A/G]ATGACTGCCCATTCA	84708
rs535399817	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53647540	GAAGTCTGCTATTTT[C/G]CCAAGAATCACTGGT	84708
rs535406602	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53466377	AACCTGAAGACAGCC[A/G]AATAGGAACAGCTCC	84708
rs535447016	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53484040	GAGGAATCTTGTTTG[C/T]CCCTCTACCATGTAA	84708
rs535458689	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53566429	GGAGAAAGAAAATAC[C/T]TTACAGACAAGCAAA	84708
rs535460272	snp	A/G	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53559848	AAATCTTTTTCAGAG[A/G]TGAGGGTCCCTCTAT	84708
rs535518831	snp	A/G	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53465526	CTGCTTTAATCTGGG[A/G]AGCCAGTACTCCAGA	84708
rs535525995	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53627965	CACAAGTCTCTGAGG[A/G]AAAAAGTGCATTTAG	84708
rs535554877	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53469957	AACTATTCCAATCAA[C/T]AGAAAAAGAGGGAAT	84708
rs535561458	snp	A/G	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53526814	CCTTCGACCTCTTCT[A/G]TTATATTGTGAGGAC	84708
rs535572516	snp	A/G	0.0240643	0.107019	intron-variant	LNX1	GRCh38.p7	4:53565302	GCAGCTGGAGATCTG[A/G]GAATGGGCAGACTCC	84708
rs535575884	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53476157	CAAAAATGAGCTGGG[C/T]GTGGTGGTGTGTGCC	84708
rs535585130	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53599336	ACCTCTGGTCGTCCT[C/T]ACTGCTACACTCCCA	84708
rs535602744	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53650136	CTGATGCTGAGGACA[C/T]GTGCCCTGCCTGTAT	84708
rs535602880	snp	A/C/T	0.00199481	0.0315187	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53503899	AGCACTTTGGGAGGC[A/C/T]GAGGCAGGCGGATGA	84708
rs535641298	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53499039	CTTAAACCCAATTTT[C/T]CCTTCAAGGCCCTTC	84708
rs535643322	snp	A/T			intron-variant, nc-transcript-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53500105	GACTGGACATCCCAA[A/T]GTTAGGTGGTCCTGA	84708
rs535645589	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53580867	AATCTCATTCCAAAA[G/T]GTACCAACATAGTAA	84708
rs535670542	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53483031	TCATCGATATGGTTT[G/T]ACTGTGTCCCCAGTC	84708
rs535703333	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507085	GCATAATGGTACTAG[C/T]GCCTGAAGGTGAGGG	84708
rs535708378	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53587245	AGGGTAAACACAGAA[A/G]GTTTACGGGAGACAA	84708
rs535749574	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53548565	ATTAGAATACTTATA[C/T]ACTGTTGGCAGGAGT	84708
rs535785277	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53554217	TTCTCCTGTCCAGCC[C/T]GCTGCCACTGGACTC	84708
rs535802030	snp	C/T	0.00398564	0.0444627	intron-variant	LNX1	GRCh38.p7	4:53498007	GGTAAACAGATCTTT[C/T]TATCCTTTCTGTTCT	84708
rs535805176	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53642815	ACCATGAGAGGGGTC[A/G]CTCCACTTGAAGAAT	84708
rs535815083	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53546393	CTGTGCAGGGTCACT[C/T]GCCACACTGTGTCAC	84708
rs535815215	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53641122	TCCTCAATGAACACT[A/G]GAATGTGGCATGGTT	84708
rs535829622	snp	A/G	0.00398564	0.0444627	intron-variant	LNX1	GRCh38.p7	4:53497267	CTATGTTGGAAGAAA[A/G]CAATTTCGCAGCAAT	84708
rs535836418	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53543309	CATGCCACTTATTTC[C/T]ATCTGATGTACTACA	84708
rs535843426	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53583733	GTCCCAAGTGGCTAG[A/T]CAATTAGACGCAAGT	84708
rs535843799	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53505135	GTCTTGAATAAACCC[C/T]TTGATGCCAAGAACT	84708
rs535843976	snp	A/G	1.66333e-05	0.00288381	synonymous-codon	LNX1	GRCh38.p7	4:53481792	GCCGGCTTCCTGAAA[A/G]ATGTCAGGGCTCCGC	84708
rs535902469	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53645405	GTTCTCAGCATTAAG[C/T]TGTCAGTGTGCACTA	84708
rs535913869	in-del	-/AT	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53544821	CCTCACAGTAGCTCC[-/AT]GAGGTTGATGCAATG	84708
rs535918675	snp	C/T	0.00199481	0.0315187	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53512032	CATTGAGTCAACTCT[C/T]ACTTTGGGTTCATTA	84708
rs535923410	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53552744	TGAGACAGGAGAATT[G/T]CTTGAACCCGGGAGA	84708
rs535947722	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53640548	ATTGCTAAAAATAAA[A/G]AATCAAAAGTGCTTT	84708
rs535947826	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53550005	AACACTTTGGACCAG[A/G]GAGTGAACAGCTTGG	84708
rs535985258	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53556180	AGGAGAAGGCAAAGA[C/G]AATTGAAGAGGACAC	84708
rs535986056	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53559010	GCTTACCCCATATTC[A/G]AGAAGATTAAATTCC	84708
rs535989187	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461319	TGAATGCTACGTACA[C/T]ACTTTTAATCCCCAC	84708
rs535996000	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53524763	TGCCCAGCTGAGGAA[C/T]TGAAGGAACTGAGGA	84708
rs536014418	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53583357	GTGATGTGTCTGTGT[A/G]TGCATGATGGGGGGC	84708
rs536058684	snp	A/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53479345	AGTAACCATATTTTA[A/T]AGAGTCTTCTTTCAC	84708
rs536073979	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53616783	TTTCCATAAAGGAAA[A/T]GGAGGCAACGATGGG	84708
rs536075361	in-del	-/C			intron-variant	LNX1	GRCh38.p7	4:53571633	GAGATGTACGTTAGA[-/C]CTCTGACCCTCAAAA	84708
rs536075460	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53540130	CTCACATCTGTAATC[C/T]CAGCACTTTGAGAGT	84708
rs536081101	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53533748	GTGCTCCTGGCATGT[A/C]GGGGGTAGAGGACAG	84708
rs536139188	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53624973	ATTGCAACAATAATC[C/T]TCTTTTACAGAGTAA	84708
rs536140564	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53627900	GGTTTCAATGGGATG[A/G]ATGTTAAGCTCTGGG	84708
rs536156755	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53581725	AATTACCTCCCCTTG[C/T]GTCCCTCCCACAACA	84708
rs536163617	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53591394	TCAACTCACCTCTTC[A/G]AGCGACTGTCTGGGG	84708
rs536165949	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53547045	TGGTTACAGCAACTC[C/T]AGTTTCTTGATCTCA	84708
rs536170763	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53486882	TGTTTTGGCATTGCA[A/T]GAATCCATACAGTGA	84708
rs536185522	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53634748	TGCTCCGAGGGGTGG[C/T]GGTTTACTAAGTCAA	84708
rs536211483	snp	A/G	0.00438332	0.0466095	intron-variant	LNX1	GRCh38.p7	4:53638439	GCTCATGGTGCTTTT[A/G]TGGTTATTTGTGGGC	84708
rs536235241	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53568137	GGGAATCCTCCCTAA[A/C]TCATTTTATGAGGCC	84708
rs536274829	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53535840	AGTTCATGAGCATGT[C/T]GGGCTGGGACTAACT	84708
rs536292591	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53623826	GCCTAGAACAATTAA[A/G]TAGCTTGCCCAAGGT	84708
rs536317324	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53509112	CCACTCGGCAAGTCA[A/T]TGCAGCGCACAGGCT	84708
rs536336522	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53535393	TGATGTTGTCACAAA[A/T]GAAATCTCTCCCGTC	84708
rs536347963	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53637806	CTTTCCCTTTTGCAG[A/T]TGAGGAAATTTCTGC	84708
rs536348594	snp	C/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53541737	ATTTGTAAGCTCAGT[C/G]TGAGTCATTAAAAAA	84708
rs536349457	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53467971	GCAGGCCAACATTCA[A/G]ATTCAGGAAATACAG	84708
rs536375677	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53532866	GGAACACTGCAGGCT[A/G]CCCAGGAAGTTGCTG	84708
rs536388768	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53492801	CGTTGGGCAAGGGGT[A/G]GAATGGGAGGAGCCA	84708
rs536389861	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53549561	GTTATTAAAGAATTA[C/T]GGTTGTTTTTGGTGT	84708
rs536399329	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53555675	TTAATTATCCCCAGT[A/G]GCATCGGGGAACAGC	84708
rs536413645	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53467713	AAGCCTCAGTAGCCG[A/C]TGCGATCAACTGGAA	84708
rs536446011	snp	C/T			intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498533	AAGTCACTATCCACA[C/T]TTATTTTACCATTTC	84708
rs536463051	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53561480	ATCCGCCCACGTCAT[C/T]CTCCCAAAGTGCTGG	84708
rs536508106	snp	C/T	0.000399281	0.0141238	intron-variant, missense	LNX1, LOC101928879	GRCh38.p7	4:53576203	TGGATGTGACAATCT[C/T]CACCAGTGCCCTGGC	84708
rs536523992	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53471757	ATCATCACTGGCCAT[C/G]AGAGAAATGCAAATC	84708
rs536539172	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53537118	GTGGGGACGGTATGA[A/G]TACTGATTTTCCTGT	84708
rs536541167	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53529828	ATGCATGACAATCAG[A/G]GCCACAGGAAATGAA	84708
rs536551595	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53536683	CTTCCTCAAATGAAT[A/G]CTTTAAATGCCTCTA	84708
rs536558141	snp	G/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53528959	CATAAAAAAAAGCCA[G/T]CACAGAGGAAAGCAG	84708
rs536571887	snp	C/G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53631519	GATCCCAATATAATT[C/G/T]CAAATCTCCCTAACT	84708
rs536576012	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53495293	AGAAAAAAAAATTTC[A/G]ACAGTGACCCTGACG	84708
rs536593692	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	LNX1	GRCh38.p7	4:53654180	TTTTTCTCCCAGAGG[A/T]TTATAACTAAGTGCA	84708
rs536604166	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53477888	CTGTGGCTCCTCAGG[C/T]TCAGCAGCTGTACTT	84708
rs536620307	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461174	CTTCTAATTGAGATA[C/T]TTCTTGCCTCTTATT	84708
rs536649025	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508373	TATATCCTCTCTTCC[C/G]TTTTCACACATCGGT	84708
rs536662068	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53485243	CCAATTACTGAGCTC[A/G]AATTTGCTCTCTTTG	84708
rs536667623	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53504172	GCTTAGTGGAGCCAC[C/T]TTCAATGATTTTAGC	84708
rs536681712	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53596266	AACCTGTGTGTTGCC[C/T]GGTTTGCAGATGAGT	84708
rs536690626	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53620831	TAGCTCACAGTGCAG[C/T]ACGCTCTAAATCAAG	84708
rs536719810	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53603138	ATCCAGAGCACCACA[A/G]TGTCACTGTATTAAG	84708
rs536731135	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53623339	TTACCAAGTAGCTGG[G/T]ACCCACCTCAGCTTC	84708
rs536734104	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53467642	AATGCAGAGAAGTCC[C/T]TAAAGGACCTGATGG	84708
rs536756264	snp	A/C/G	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53610799	ATAAATAAAGGCAAA[A/C/G]GCTTAAATTACTGAA	84708
rs536756560	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53610133	TTATTGTTTTTCATA[G/T]GTCCGCAGAACATTT	84708
rs536769244	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53492942	ACATGAATTTGGGAA[C/T]AGATGGCATACACCT	84708
rs536772612	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53629687	AAAAAGACACTCCTG[C/T]TCTGTGTTTGTTCAA	84708
rs536792201	snp	C/G	0	0	intron-variant	LNX1	GRCh38.p7	4:53561451	CATGATGGTCTTGAT[C/G]TCCTGATCTCATGAT	84708
rs536797485	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53471671	CCCATCAAAAAGTGG[G/T]GAAAGGATATGAACA	84708
rs536799345	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53467320	AAACAGAAAGGGCAT[C/T]GACACCAAAAACCCA	84708
rs536809570	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53624375	TCATGAGATCTGATG[A/G]TTTTATAAGGGGAAA	84708
rs536816845	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53515742	TAAACACTCATGGGA[A/G]GGTCTTCTAAGAAAG	84708
rs536825266	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53642881	CACCCTCTGAGGACC[A/G]TTATGGTCGCCTGGG	84708
rs536826623	snp	A/G	0.00199481	0.0315187	intron-variant, synonymous-codon	LNX1, LOC101928879	GRCh38.p7	4:53576117	ATTTGGGAGCCAGCG[A/G]CCCCTCCTTGATTCT	84708
rs536864492	snp	C/T	0.00279162	0.0372561	intron-variant	LNX1	GRCh38.p7	4:53494402	TCAGCAGCAAGAGAA[C/T]GGACTAACACATGGG	84708
rs536865807	snp	G/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53649100	AAATGAATCCAAAAG[G/T]TTCTGATTTTACTCA	84708
rs536870776	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53583642	AGGGAGACCATGTAA[C/T]ACATCTGGAGTCAAT	84708
rs536878683	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53603193	GTGCTGGCCGTGGGG[C/T]CATGGAGGACTCCAG	84708
rs536924215	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53470959	CCCATCGAGCTACCA[A/G]TGACTTTCTTCACAG	84708
rs536937430	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53630771	AATGTTGTCACCAGA[A/G]GATCATAGGAAGCTA	84708
rs536950707	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53616788	ATAAAGGAAATGGAG[A/G]CAACGATGGGTTACT	84708
rs536975508	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53637738	AAACACAGCCAGTTT[A/C]TGAGATATTAAAATG	84708
rs536994994	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53471355	TCAAGATGGATTAAA[A/G]ACTTATATGTGAGAC	84708
rs536995876	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53628451	GAGACACCATATTAC[G/T]CCTGCAAGAATGACC	84708
rs537016881	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53637326	TTATGACCCACTAAA[C/T]GAATCTCTTTGTACC	84708
rs537066590	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53588666	GGGGCCTGTGAAGTA[C/T]ACCATTTTAGCGTCC	84708
rs537139601	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53636436	TCTTTGGGACTCTGG[C/T]GAGACATTCTTGTCC	84708
rs537160848	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53602459	AAGCCTGTCTTAGGG[C/T]CCTGCAGCACTCAGT	84708
rs537161408	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53548021	GATCCTCCAGTTCCA[A/G]TCTTGGTGGTAATGA	84708
rs537185654	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53649024	TGGAGGCTGAAACGA[C/T]AAAAAAATTATGGTG	84708
rs537197185	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53554933	CCAAATTTGAATCCA[C/T]GTACTGGATTAGTTC	84708
rs537206608	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53568670	TGGCCAGGGCAATTA[G/T]GCAGGAGAAGGAAAT	84708
rs537210703	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53471321	GGATCCCTTCCTTAC[A/T]CCTTATACAAAAATT	84708
rs537216578	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53486747	GGACTGGCTTTCTGT[C/T]GTTTTGTTTAATGAC	84708
rs537220265	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53608162	CAGCAAAAGAAGTGA[C/T]CAACAGAGTAAACAG	84708
rs537254085	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53512433	CTTTCTCAGTCCTCT[A/G]GAATGCAACACTACC	84708
rs537267280	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53568072	TACCAGAGGTACAAG[A/G]AGGAACTGGTACCAT	84708
rs537269483	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53477777	CAGCAAGAGCAAAAA[C/G]ACAGGAGGAGAAAAA	84708
rs537284711	in-del	-/AT	0.242239	0.24988	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53594144	GTGTGTGTATAATAT[-/AT]ATATATATATATGTA	84708
rs537304001	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53536030	TAATTACTTGACCCT[G/T]CCCCCAAGTCCTCCT	84708
rs537306122	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53528005	CTATGTGCCAGGTTA[A/T]TATCTTCTAAGTTTA	84708
rs537307984	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53582796	GCTTAGTTTCAAACT[C/G]GTCACTGGGGTGACA	84708
rs537338897	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53630520	TTTCTTGGTGATTTT[C/G]CTGTTTAAAATGGCC	84708
rs537354818	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53542553	GAGCAAGTGTCACAA[A/C]ATTTATGGATGACAC	84708
rs537363906	snp	C/G	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53535278	TTTGTTGTTTTGGAT[C/G]CTTAAGCCATGACTC	84708
rs537380059	snp	A/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53501902	CAGCCCGCCTACTCA[A/T]TGAACATGGCTGCTA	84708
rs537381688	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53630384	CAAAAATTGGAGTGA[A/G]AGGACACACACATTA	84708
rs537391033	snp	C/T	0.00398564	0.0444627	intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53575130	GGGATTACAGGCGCG[C/T]GCCACCATGCCTGGC	84708
rs537394653	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53481191	AGAGTTTTCTGGATT[G/T]GAATGCCATATAACA	84708
rs537402674	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53622653	ATATAACAAAGGAGG[A/C]AGTTCATGAGATTGA	84708
rs537425934	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53589366	TTTCCAAACTGTTAA[C/T]ATTGCAGTTAATTAC	84708
rs537430148	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53571558	AAGAGGCAAGGAAAG[C/G]GATTCTCCCCTGAAG	84708
rs537437694	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53492787	CCTAGGGGAGAGCAC[A/G]TTGGGCAAGGGGTGG	84708
rs537451252	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53540912	GAGGCTGAGACGGGC[A/G]GATCACTTGAGGTCA	84708
rs537451825	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53492079	GGCATGAGCCACTGC[A/G]CTTGGCTGAGGATAT	84708
rs537457126	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53641303	CTTCTGGCCCCAAGA[A/G]GGGACTTACCCAGAT	84708
rs537465067	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53578229	TTTAAATCTCTTCAG[C/G]CTCTATTGCAAGTAG	84708
rs537484302	snp	C/T	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53534686	ATTTTGGTCACTTGG[C/T]GTAAAACAACCTATT	84708
rs537485188	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53538553	TAATCTGAATAAGCC[C/T]TACAATAGGAAAAGT	84708
rs537500069	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53584907	ACGTATATCACATTT[G/T]CTTACTCAAAACATG	84708
rs537506597	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53587819	AAGACCCGCTGTTTA[C/T]TCACATCACAGAAGC	84708
rs537529867	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53639626	CTAAGTAGAATGGAC[C/T]GTTTTGGGGTCCTAA	84708
rs537539489	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53612652	TAGCGAGACCCTGTC[C/T]CTACAAAAAAATACA	84708
rs537547379	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53540885	CTGACGCCTGTAATC[C/T]CAGCACTTTGGGAGG	84708
rs537574807	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53632472	TGCTTCAGCCAAGAG[G/T]GTCAGTCAGACAATG	84708
rs537578596	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53478453	GTAACAAAAGTCCTG[A/G]CCGATCACTCCCACA	84708
rs537600364	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53485678	TATAAGGTGGAAAAC[A/G]GGCTAATATGCTTGT	84708
rs537612966	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53469309	AGAACAAAGACACAG[C/T]GTACCAGAATCTCTG	84708
rs537630781	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53514407	TCATGGACACACAGT[C/T]CCACCTGGCTGGGGA	84708
rs537634566	in-del	-/A	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53472487	AACTTAAAGTATAAT[-/A]AAAAAAAAGAAGAAG	84708
rs537656410	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53495446	GGGGCTTCCTCTCAG[A/G]TTCATACTTGGGTTT	84708
rs537688316	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53520887	GAATCACTTGAACCC[A/G]GGAGGTGGAGGCTGC	84708
rs537725577	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53615984	GTTGTGCTATCAAAT[A/G]GCAGGTCTTACTAAT	84708
rs537762347	snp	C/T	0.00438332	0.0466095	intron-variant	LNX1	GRCh38.p7	4:53527425	CTGAGAGTGAGTTTG[C/T]ATGAATTCCCCCACA	84708
rs537775219	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53523665	AGGAGACTAGGAGAC[C/T]AGGGATTTTTCTGCT	84708
rs537810357	snp	A/G			upstream-variant-2KB	LNX1	GRCh38.p7	4:53652809	CATGCACCAAAATCT[A/G]TATCAGGCAAATAAG	84708
rs537820530	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53506816	AGCCGAGATCATGCC[A/G]CCGTTGCACTCCAGC	84708
rs537828654	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53650159	GCCTGTATGGAGGAG[A/G]CAGCTTTGTCCCCCA	84708
rs537829595	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53578994	TGTATGATGTATCAC[A/G]TTTTCAGACATATCA	84708
rs537855329	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53488633	AGGGGATTGTCTCTA[C/T]GCTCTATGAATCCAA	84708
rs537863658	in-del	-/A	0.0201919	0.0984289	intron-variant	LNX1	GRCh38.p7	4:53467592	AGTTAAAAACCTTGA[-/A]AAAAAAATTAGACAA	84708
rs537868541	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53585296	GAACATAGAAATAAA[C/T]GAAGGTAGTGATGAT	84708
rs537889385	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53515938	TGGGCACAGTGTTTA[C/T]TTACCATGAGGTTTA	84708
rs537902362	in-del	-/AGTT	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53465489	GGAGGCACTGTATTA[-/AGTT]AGTTACATTCTTCTC	84708
rs537937835	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53632956	AGAATCCTTTTGTAG[A/G]TTCTACTTCTAGACA	84708
rs537965241	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53624812	AAATTTATTCAATGA[G/T]TAATTAACTAAAATA	84708
rs537969921	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53495922	AAGGGAGGCACTGCA[C/T]GACACATGTGGTAGT	84708
rs537993532	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53479237	GCACCCAAAATTTCT[A/C]AAGTGAGTCATTTAT	84708
rs538010160	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53645424	CAGTGTGCACTACCA[C/T]TGGGGTTACCCAATG	84708
rs538015188	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53639255	CAAATACTGCATGTT[C/T]TCACTTGTAAGTGGG	84708
rs538017550	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53651366	TGACACATGACCAGT[C/T]AGTGTTGGAGCAGGG	84708
rs538022894	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53518843	ATGGAAAATTAGAAG[C/G]AGGTTTTTCATAACC	84708
rs538037638	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53551826	GGCCTCTCACCCTGC[C/G]TTATGACCCTTGGTT	84708
rs538053845	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53644874	GGAGAGATGTGGTAA[C/T]AGGGAGGAGGAAGTC	84708
rs538077828	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53518072	AATGAACACCAGACA[A/G]GAAAAATTCAAAACA	84708
rs538088471	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53550993	GGCCTGTGAGCCCCA[A/G]AATGAATGTTCTTGT	84708
rs538120042	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53474701	GAAAATCAGTGTTGT[C/T]TATGCCGGGATATCA	84708
rs538141522	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53550743	AAAAGGCACTTCCCC[A/C]GGTCCTGGAGTTCAT	84708
rs538158310	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53620002	TTTAATATTCTTATA[A/G]ATTTAAAAGATTAAG	84708
rs538164060	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53532203	GCAGGTGGCTAGGCA[C/T]GGTGGCTCATGCCTA	84708
rs538180079	snp	A/G	0.000103425	0.0071904	intron-variant	LNX1	GRCh38.p7	4:53481676	GCAGCCTTCCCAAGA[A/G]ATAGCCCCTTGCAGG	84708
rs538187861	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53644353	GTTGCAGTGAGCCGA[G/T]ATCACGCCACTGCAC	84708
rs538200423	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53473127	TTGATAACCAACCAT[A/T]TTACTATGAATGTAA	84708
rs538202888	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53556965	GCCAACTCTTGCTAT[G/T]TTTCCCGTCTGGTTA	84708
rs538205535	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53468161	GCAGAAACTCTACAA[A/G]CCAGAAGAGAGTGGG	84708
rs538211917	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53477492	AAGAAAAACATTTTC[A/C]TTGCTAAGGTGAAAA	84708
rs538226386	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	LNX1, LOC101928879	GRCh38.p7	4:53577081	GAGGGGGTAAAGTTG[C/T]TTCAAGGAAATCTGT	84708
rs538227062	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53612799	CTGAGCTGGGAGGAT[C/T]GCCTGAGTCCAGGAG	84708
rs538260434	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53479993	ATGCAAAATTTGATG[C/T]CTAGCATTCCTTAAC	84708
rs538260718	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53562065	ACAACTTATTTTTCT[A/T]TCATTCAGGGCCTGA	84708
rs538295110	snp	G/T	0.00318978	0.0398085	intron-variant	LNX1	GRCh38.p7	4:53530243	TAAAATATACAGAAA[G/T]AATCGTAAGTAAAAA	84708
rs538308878	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53539361	GTCCTTTAGTTTCTC[C/T]TTATTGTATTAGTTT	84708
rs538310798	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53590357	CTAACTTAAATCTCA[A/G]AAAAACAGCTGATGT	84708
rs538373157	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53570081	GGACTGTAAACTAGT[A/T]CAACCATTGTGGAAG	84708
rs538382411	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53638520	GAGGTCCAACAGTGA[C/T]GCTCTGGCTTCTTGT	84708
rs538404416	snp	A/C	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53473972	GTTAAGTAAAAAGAC[A/C]AAGCCACATATGGAG	84708
rs538410716	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53571953	GGTGTGAGCCACTGC[A/G]CCCAGCAATTTGGGT	84708
rs538417537	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53502265	GGCTGCTATGGTCAT[C/T]AATTTATACTTCATT	84708
rs538417962	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53463754	TGAGTATGGTGGCTC[A/G]TTTGATTTCCACTGA	84708
rs538427343	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53503559	ACAGTGGGCTTAAAA[C/T]ATTGAGTAAACTATG	84708
rs538434577	snp	A/G	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53495494	CACCTGGACTTAGCC[A/G]TGGAGACTAAGACTT	84708
rs538447963	snp	G/T	0.00279162	0.0372561	intron-variant	LNX1	GRCh38.p7	4:53540139	GTAATCCCAGCACTT[G/T]GAGAGTCTGAGGCTG	84708
rs538449375	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53571510	GGAAGAGGAGGCCAC[A/G]AGCCAAGGAAGACAG	84708
rs538473433	snp	C/T	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53590570	TCCTAGAGGTAAAAT[C/T]ACTTTAAAAGCCAGG	84708
rs538495058	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53612437	GTTTTAGCTTGCTTC[C/T]TTTACTTTGTTTTGT	84708
rs538509056	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53597719	CTTCTAGCTTTGTTT[A/C]CCTTGTTCTAACCTT	84708
rs538514740	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53557445	TTTTACTGATACTAT[A/C]CCTGTTTTCAGGTAT	84708
rs538547969	in-del	-/AAAAAAAAAAG			intron-variant	LNX1	GRCh38.p7	4:53541137	GCGAGACTCTAACTC[-/AAAAAAAAAAG]AAAAAAAAAAAAGAA	84708
rs538587375	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	LNX1, LOC101928879	GRCh38.p7	4:53577977	TGTGCTAGGGGCCTT[A/G]TATTATAGTATATTA	84708
rs538592730	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53480312	GACATATGACAGAGG[G/T]TTGCAGCAGAAATGT	84708
rs538600111	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53632273	CTTCTGGGCTCCCAT[C/G]CTCCCTTTTCTCTCA	84708
rs538604865	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53584845	TTCAAATAGCTAGTG[C/T]TTCCCACGTTACTTT	84708
rs538610425	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519055	TTATCATTGCTGCAT[A/G]CCTCATAGGTCAGTG	84708
rs538645008	snp	C/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53495430	GTCCCTCTCTTCTTA[C/G]GGGGCTTCCTCTCAG	84708
rs538645796	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS2	GRCh38.p7	4:53591331	ATTCCGTGTTCAGAT[A/C]CCTCAGGGGCCAGTG	84708
rs538678218	snp	A/G	0.00279162	0.0372561	intron-variant	LNX1	GRCh38.p7	4:53529644	GCATCTGACAGCTCC[A/G]TGTACATTGTGAGCT	84708
rs538707312	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53502565	GCTGACTGATCACAG[C/T]GGTGGTTGCTGAAGG	84708
rs538723372	snp	G/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53624326	ATCATGGGGGCAATT[G/T]CCCCCATACTGTTCT	84708
rs538739801	snp	C/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53528997	CAATACAGAGAGAAT[C/G]CATATTGATGTAGTT	84708
rs538769311	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	LNX1, FIP1L1	GRCh38.p7	4:53462953	TCATGTACAAAGCAG[A/G]TAACTGGCTATTCTG	84708
rs538772564	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53630703	TATATTAGATGCGGT[A/G]TATTTAAATAGGAAC	84708
rs538809605	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53504877	TATAAGGGCATGGCT[C/T]GTGGCACGCTAAAAC	84708
rs538820509	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53550105	TGAAACAGGATCACA[A/G]TGCTCTTTGGACATC	84708
rs538822007	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53644290	CCTGTAGCCCTAGCT[A/G]CTTGGGAGGCTGAGG	84708
rs538822075	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53617757	ACAGAGATGTTATTG[A/G]CTAAACCTGTAACAA	84708
rs538838530	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53462102	TACACCCAGTGCTAC[A/G]TTTGATAAGTCATAG	84708
rs538850702	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53650126	TTCTTCAGGCCTGAT[A/G]CTGAGGACACGTGCC	84708
rs538855717	snp	A/G	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53563141	AATCCCGGAGGCAGA[A/G]CTTGCAGTGAGCTGA	84708
rs538864603	snp	A/C	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53619935	AAGTCAGCTGGTGTT[A/C]TTACTAATTAAGAAC	84708
rs538867656	snp	A/G	0.00755907	0.0610114	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53523444	GGCGTGCACCACCAC[A/G]CCTGGCTTATTTTTG	84708
rs538888910	snp	C/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53595209	TGGAACAGGAATGAT[C/G]ATAGCAGATATCTGT	84708
rs538927560	snp	A/C/G	0.00358923	0.042236	intron-variant	LNX1	GRCh38.p7	4:53531164	ACTTTCTTGCTTCCA[A/C/G]TAAGTTAAACTCAGC	84708
rs538941097	in-del	-/C			intron-variant	LNX1	GRCh38.p7	4:53642676	AATCACAAACACTGG[-/C]CCTTTTGGAGAGATC	84708
rs538953886	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53530660	GTAAAAAAAGTAGTA[G/T]TATTTAGGATAGTGA	84708
rs538959797	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53625513	GATTAAAACCTAAAT[A/G]AGGCTAGGTGTGGTG	84708
rs538963553	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53610934	GAGGAAATGCAAAAT[C/T]ATAAAAGATCAGAAA	84708
rs538964240	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53521875	CATCATCATAGCTTA[C/T]CACAGCCTCAAACTC	84708
rs538988953	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53649815	GAAATTTATTGCTTG[C/T]CTGCTTCCCACAGTG	84708
rs538994351	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53479195	TGCTCCTGGCCATGG[A/C]GGAATCTTAAGCACA	84708
rs538994439	snp	C/G	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53471794	ACAATGAGATACCAT[C/G]TCACACCAATTAGAA	84708
rs539012622	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53562038	AAGGTCATTTCCTTA[C/G]AGGCAGAAATCACAA	84708
rs539028008	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519756	TTCATTTAATCTTCA[C/T]AACAACCTCATGAGA	84708
rs539037422	snp	A/C	0.00119737	0.0244387	intron-variant, missense	LNX1, LOC101928879	GRCh38.p7	4:53576096	CGGGGACTTGGCCAG[A/C]GTGGTATTTGGGAGC	84708
rs539042819	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53486699	ATTCAGAGAAAAAAA[A/T]GAGGGTTAAAACTAA	84708
rs539046617	snp	C/T	0.00557542	0.0525036	intron-variant	LNX1	GRCh38.p7	4:53569201	AAAGAGCCCCCATTG[C/T]CAAGTCAATCCTAAG	84708
rs539063152	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53610253	AATAAATAAGAAAAA[A/G]TTATCAAAAGGTAAC	84708
rs539066134	snp	G/T			intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53575330	CAATACATATTTTCC[G/T]TTAACATAGATAGGA	84708
rs539082130	snp	C/T	0.0126979	0.078662	intron-variant	LNX1	GRCh38.p7	4:53564798	GCGCGCACCCTGCGC[C/T]AGCCGAAGCAGGGCG	84708
rs539097934	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53616876	TGGCTTGAAATGTAG[C/T]TAGCTGTGTGGTTAC	84708
rs539124883	snp	C/G			nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53604920	GTAAAATGTAAATGA[C/G]TGATGAAACAACATC	84708
rs539125454	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53596478	AAAAAAGAACTTCAT[A/T]GTTACTGTGTTTATA	84708
rs539134121	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53621591	TACAGTCCACTCTGT[C/T]GCACTCATATAACTC	84708
rs539139648	snp	C/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53595116	ATTTCATGAAGAAAG[C/G]AACATGAATTGGGCC	84708
rs539149192	snp	A/G	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53464994	ATAACTTTTGCAGCT[A/G]TGCAATATCAAATTT	84708
rs539160393	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53564177	TGAGTGTTCATCAAG[C/G]CTCTATCTCAGGCTT	84708
rs539160415	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53627817	TAGAAGTGCTTGAGT[G/T]AGAGCAGAAACCCTC	84708
rs539170924	snp	A/C	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53620715	AAAATAAAAATAATA[A/C]GAAAAGAAAAATTAT	84708
rs539188330	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53637908	TGGACTCCACCCAAC[C/G]AGACCTAGTGATTTT	84708
rs539192561	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53468349	TGGAGGAAGCACTAA[A/C]TATGGAAAGGAACAA	84708
rs539201293	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53580745	GTCTTCAGTGGCTAA[A/G]TAGTTCAGTACTGGA	84708
rs539210346	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53641752	GCTTGCACATTCCAG[A/T]ACTCCATATAAATGA	84708
rs539215794	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53547335	ATGTACCAGGCACTA[C/T]ATTAAATGCTTTACA	84708
rs539217282	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53502068	ATCTTCTGTATTGGT[C/G]TGGAAAGAAAATGAT	84708
rs539224995	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53643793	GAAATAACAATAGGA[C/T]TTTTCAGAATTATGA	84708
rs539228982	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53466597	TCCTAGTCAAAGAAA[A/G]GGGTGACAGACGGCA	84708
rs539231107	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53554068	ATAGGAGACGGATGA[C/T]GTCCTTTCTTTTGGG	84708
rs539236293	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53501805	ACGACATTGATACCA[A/G]GCTAGCTGAGTCTTA	84708
rs539239428	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507067	AATTATTCTTCCTCA[C/T]ATGCATAATGGTACT	84708
rs539249144	snp	A/G	0.000806614	0.0200663	intron-variant	LNX1	GRCh38.p7	4:53647486	GACCAATTTCTAACC[A/G]AGAGATATTTTTCTG	84708
rs539261989	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53641238	TTTACTCTCTAAGAA[A/G]GAGGGATTTCTAGCT	84708
rs539266722	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53596990	TGGACTGTACTGTCT[G/T]GTTCCTGGACTCCGG	84708
rs539283949	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53611472	TTGTTTGTTGTTTTT[A/G]GTAATTGGATAAAGT	84708
rs539306383	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53562579	AATGAAACGCATTCT[A/G]GAGAAAACAGGCACC	84708
rs539325103	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53491549	TCAGTCAATAATCAC[A/T]GAACAAATTCAAGGA	84708
rs539331125	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53553431	GAGCCCTCCAAATCT[A/G]CATTTTGAAAACAAA	84708
rs539385339	snp	A/G	0.0107246	0.0724382	intron-variant	LNX1	GRCh38.p7	4:53472254	AAAAAACCAAATACT[A/G]CATATTCTCACTCAT	84708
rs539391143	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53646867	TTTTCACTATTATTT[A/C]ATTATTGTTCCAATT	84708
rs539394318	snp	C/G	0.0115144	0.0749975	intron-variant	LNX1	GRCh38.p7	4:53652057	AGAGAGAGAGAGAGA[C/G]AGAGACAGAGAAAGA	84708
rs539401138	snp	A/G	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53470042	AGACACAACAAAAAA[A/G]GAGAATTTGAGACCA	84708
rs539401357	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53476057	ATCCCAGCACTTTGC[C/T]AGGCCGAGGCAGGCA	84708
rs539431976	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53504240	AGCATTTGCTGCTTC[A/G]TTACAATCAGCATCT	84708
rs539441790	snp	A/G	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53592340	GACCCTGGACAAGTC[A/G]CTGGTTGCTTCACCT	84708
rs539467999	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53614005	TTTTTTGATAATAGC[C/T]GTTCTGACTGGTGTG	84708
rs539474933	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53599296	CCAGCTAAAACCCAC[A/C]AAAACCAAGATGGCT	84708
rs539495824	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53486591	CAGGGACAGTCAGAT[C/G]GGAGTGCCATGAAAG	84708
rs539513625	snp	A/G	0.00398564	0.0444627	intron-variant	LNX1	GRCh38.p7	4:53606078	ACACAGTTAGCAGAA[A/G]ACAGGAAATAATCAA	84708
rs539529634	snp	G/T	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53469245	CTGAATGACTACTAG[G/T]TACATAACGAAATGA	84708
rs539531101	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53484255	TGCATCTTCATTCCC[A/C]GAGCACACAACTCAC	84708
rs539547691	snp	G/T	0.000798403	0.0199641	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53605641	TTTCTCTGTATTCAT[G/T]TTTTTTTTAAAATTC	84708
rs539556393	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53482830	TGTAACCAAAAACCA[C/T]GTGTATTCCTAAAGC	84708
rs539568906	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53517103	GCAAAGAGCACTGGC[A/G]GACAGGGTCTGGCAG	84708
rs539583792	snp	C/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53572914	CTTAATTGAGAACAC[C/G]TCACACCTTCTTGAA	84708
rs539591336	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53468878	AGACTTAGACTCCCA[C/T]ACAATAATAATGGGA	84708
rs539606443	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53628214	GAAACAGACAACCCA[C/T]AGAATAGGAGAAAAT	84708
rs539617517	snp	A/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53510216	ATTCATCTGAATGGA[A/T]TTCAAAGCCACAAGA	84708
rs539620319	in-del	-/GGGCACAAGACAGGG			intron-variant	LNX1	GRCh38.p7	4:53568595	GGGCACAAGACAGGG[-/GGGCACAAGACAGGG]GGGCACAAGACAGGG	84708
rs539634566	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498314	AAAGAGATAAAAGGA[A/G]AAAGAGGAGGTGGAG	84708
rs539653064	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53497167	GGCCCTCTCATTTGT[A/G]CCTCACTAATGATGT	84708
rs539678783	snp	A/G	0.00358779	0.0422022	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53594163	TATATATATGTATAT[A/G]TAAATATGTATATAT	84708
rs539684027	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53466333	TTTGATTAAAATTTA[A/C]ATGATCGTAAAAAAT	84708
rs539687963	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53512900	TGGTCACTGGGAGAC[G/T]GAAATGGGCTCTCCC	84708
rs539696169	snp	A/G	0.00398564	0.0444627	intron-variant	LNX1	GRCh38.p7	4:53652058	GAGAGAGAGAGAGAG[A/G]GAGACAGAGAAAGAG	84708
rs539698757	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53585450	TGGGTAGAATGAGGG[C/T]CCCTGCAAAAGATAT	84708
rs539710997	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53581615	GCAGGCGAGAGAACA[A/T]GTGCAGGGGAACCGC	84708
rs539713913	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53504961	AATAATGAAAAAGTT[G/T]GAGATGCTGCAAGAA	84708
rs539726910	in-del	-/A	0.28578	0.247426	intron-variant	LNX1	GRCh38.p7	4:53554852	GCGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA	84708
rs539730952	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53607946	AGTACCCATTTCTTA[C/T]ACCATATACAAAAAT	84708
rs539739570	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53538750	TGCTGCACAAAGATT[C/T]GAAATGCAGCAGCCA	84708
rs539767567	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53559768	TCCTCCTGCCTCAGC[C/T]TCCCAAGTAGCTGGG	84708
rs539772660	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53633234	GAAAACCTATGGCAC[A/G]TAACAGGGATTCAGT	84708
rs539792619	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53470589	TGAATATCTAGAAAA[C/G]CCCATCATCTCAGCC	84708
rs539799980	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53464883	TAGAGTCAAATTTAA[A/G]TTATCTCTCAGTGAC	84708
rs539804805	snp	C/T	0.000214371	0.0103508	intron-variant, synonymous-codon	LNX1	GRCh38.p7	4:53557948	CCAAGGCAAGACCAG[C/T]AACAGAAGCGCCTTC	84708
rs539808462	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53645821	AATAAAGATGTTTTG[A/G]ATGAATATCTGAAAC	84708
rs539818210	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53552072	TAATGAATATTGTTC[C/T]TAGTGATTCCACTTA	84708
rs539827309	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53651183	TGTAAGCAAATGTTC[A/C]CTCAACAAATTCCTC	84708
rs539867532	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53468602	AGGAAACCCATCTCA[A/C]GTGCAGAGACACACA	84708
rs539871968	in-del	-/TAAATA			cds-indel	LNX1, FIP1L1	GRCh38.p7	4:53460818	AATGTATTCTTTCTT[-/TAAATA]TAAAAACTGACAAGA	84708
rs539899866	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53633484	AAAAATGCATGACAA[C/T]ACTCAGAAATACTGA	84708
rs539923836	snp	A/G	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53612820	AGTCCAGGAGTTTGA[A/G]GCTGCAGTGATCTGT	84708
rs539944436	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53531342	CAGCTCACTTCATTC[C/T]CTTAAGTAAATCACT	84708
rs539957148	snp	A/C	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53524648	ATATTGTCTCCAGGG[A/C]TGACTCAATTCCTAG	84708
rs539981373	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53650992	GCTGAAGACAACGCT[A/G]TGAGGGATGTATTAC	84708
rs539982241	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53615651	AGGTTGTTGTTTTAA[A/G]GTATTGAGTTTTGAA	84708
rs539983087	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53637646	GTAGAATGTGCAACC[G/T]TATTTTTTGTGCCCA	84708
rs539985832	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53473639	GGGTGACAACAGACA[C/T]CAGGGCCTACTTGAG	84708
rs540027290	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53585866	GTTTATGGGTATTTG[G/T]TATGGCAGCCCTAGA	84708
rs540041794	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53586388	TAGACCTCCCCATCA[C/T]GCATGTGCTATTGTG	84708
rs540053203	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53552356	AGAATATGGCACAAA[C/T]GTGAGAATAATTTTC	84708
rs540058009	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53539339	GGGCTGATAAAAATG[C/T]TCAGATGTCCTTTAG	84708
rs540066427	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53490706	GCAAATGTGATTCAC[A/G]GAGTAGACATACAAA	84708
rs540080521	snp	C/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53592852	TAGCTCGCAAAGCAA[C/G]GGGGAGGAGAAGGAA	84708
rs540125077	snp	A/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53465041	TTGTTATCAAGTTAC[A/T]TCCTAACAATTTATG	84708
rs540136054	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53546090	GAGATTACAGGCATG[A/G]GCCACTGCACTGGGC	84708
rs540141106	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53545179	AATGACTTTGAGAAC[A/T]CCTGTAGTCTGCTCT	84708
rs540143575	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53464391	GACTAATACTTTATC[A/G]TTAAATAAAAAATGA	84708
rs540148412	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53545419	AATCCATCTCCATGA[A/C]AACACAGTAGCGATG	84708
rs540150009	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53540631	AGGTTGCAGCGAGCC[A/G]AGATTGCGCCACTGC	84708
rs540153201	snp	C/T	0.00318978	0.0398085	intron-variant	LNX1	GRCh38.p7	4:53640481	TCTATGGCCTTAGTG[C/T]TTCTCTGCTTAGGAT	84708
rs540155796	snp	A/T	0.00597247	0.0543191	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53598962	GCTAAGGACAAACAA[A/T]TAAAGTGTAAGGTAG	84708
rs540162423	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53558331	GAGCAGACAGGCTGG[C/G]AGTTAAAATGTGTTG	84708
rs540171778	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53514984	ATACCCCATCCAAAC[A/G]ACATATTTAATGAAT	84708
rs540183014	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53468979	TGAACTCAGCTCTGC[A/C]CCAAGCAGACCTAAT	84708
rs540208174	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53556243	CAGAGGTAGAGTTAT[A/G]CAGCCACAAGCCAAG	84708
rs540209010	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53631216	GTGAGAGTGAAGGAT[C/T]GGGAGTGGGGTGGGA	84708
rs540248340	snp	C/T	0.00398564	0.0444627	intron-variant	LNX1	GRCh38.p7	4:53563637	CCTCCCAGGTTCAAG[C/T]GATTCTCCTGCCTCA	84708
rs540251873	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53474229	TTGTTTTTAAATAAA[A/T]TGCATGGTACATAGG	84708
rs540252996	snp	A/G	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53494910	CAGTCCCCCAAGTCC[A/G]TATATGATTTCATTT	84708
rs540257793	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53517478	CATGCTACTTGGAGG[A/T]CACTCAAGTAACAAT	84708
rs540270358	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53605751	TTGTCACAAATGAGA[A/G]GATCTCCTTTTTAAC	84708
rs540279834	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53472067	GCACTATTCACAATA[A/G]CAAAGACTTGGAACC	84708
rs540282496	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53550287	TGAGCCCAAATGGGC[C/T]CTGGCTTTGCCCCAA	84708
rs540284271	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53646128	ATGACATCCATACCT[A/G]GTTTGTATTTCTATT	84708
rs540314042	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53523855	TTCACACTGTCCCAC[A/C]ATCCTCCTGCTTCCC	84708
rs540317590	snp	A/G	0.00358779	0.0422022	intron-variant	LNX1	GRCh38.p7	4:53589320	ACCTTGTTTGATGAC[A/G]TTGTTTAAGAATTCT	84708
rs540331609	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53597226	TATCAATTGATATTC[C/T]TGATCAGTCCCTCTT	84708
rs540363337	snp	G/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53481291	CTTCCTGGGCCCTTC[G/T]GCAAACACAAACAAA	84708
rs540375475	snp	C/T	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53545789	CTCAGATTTGAATGA[C/T]TTCAGAGGCCACATT	84708
rs540392929	snp	G/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53530855	AGAAAAAAGGAGGGG[G/T]TACAGGGAATTAAAA	84708
rs540469725	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53571006	CACTCCAACCTGGGC[A/G]ACAGAGCCAGACTCC	84708
rs540482371	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53504455	GGTTTAAGGGAATGT[G/T]GTGGCTGTTTTGTTT	84708
rs540483410	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53613507	CTGATCCTCTCCGTC[C/T]TCCACCCCCCACCGT	84708
rs540490708	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53503959	GCCAACATGGCGAAA[A/C]CCTGTCTCTACTAAA	84708
rs540498923	in-del	-/AATT	0.00478085	0.0486577	intron-variant	LNX1	GRCh38.p7	4:53480481	TTGGATAAAAACTTC[-/AATT]AATTAATTAAGCTAA	84708
rs540505673	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53537442	TGTGGGTTTCTTCTA[C/T]CAACAGGTGGCCAGA	84708
rs540511514	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53485867	GTTTATTTCACACCT[A/C]TGTGATATGTACCAA	84708
rs540556022	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53646366	TGGCTCCCCCACCCC[A/C]TTCTCAGTCTCTATC	84708
rs540558971	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53631908	CTCGGTGTAATTCTA[G/T]AGTTGTTAGATGTTT	84708
rs540566737	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53536979	TGTTAACAGTGATGA[C/T]TTCTAATTACTTAGG	84708
rs540567553	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53645506	CAAGGGCCACTGAAA[A/T]TGCCTTCTGAGTAAT	84708
rs540568144	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53625171	CCTTGGATTAGGCAA[C/T]GGTTTCTCAGCTATG	84708
rs540572981	snp	C/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507917	ACAGAACTTTCCACA[C/G]TAAGTATTCCACAGA	84708
rs540573991	in-del	-/TAGCT			intron-variant	LNX1	GRCh38.p7	4:53648193	TACCATGTTACACAA[-/TAGCT]GTATCAGTCTACATT	84708
rs540575410	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53573243	GGGCTGGGGGAAGGT[A/G]GAATGGGGAATTCGT	84708
rs540587465	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53635940	AAAATAGCAGTGTGG[A/G]CTGATACGGCCAGTG	84708
rs540587551	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53628389	AGAAACATGGAAAAA[C/T]GTTCAACATCACTAA	84708
rs540607618	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53499207	CAGGGTCTTACTCTG[C/T]TGCCCAGGCTGGAAT	84708
rs540624397	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53635110	GCTGGAATAGCACGC[A/G]TGAGCCATGGTGCCC	84708
rs540640906	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53497999	TTCTGCCTGGTAAAC[A/C]GATCTTTTTATCCTT	84708
rs540671415	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53641869	CAGTTCATTCCTTTT[A/T]TTCTGCTTAGTATTG	84708
rs540672239	in-del	-/AGGG			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53601092	GAAAGAAAGAAAGAA[-/AGGG]AGGGAGGGAGGGGGG	84708
rs540701576	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53594865	CACAGGCACGTGCCA[C/T]CATGCCCTGCTAGTT	84708
rs540702108	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53462376	ACTATGTTATAATTG[C/T]CATAGAAGTGTGTGT	84708
rs540727994	snp	A/G	0.0178098	0.0926698	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53601104	GAAAGGGAGGGAGGG[A/G]GGGGGGGAGGGAAGG	84708
rs540728419	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53525763	AGGCAATCCTGTTAA[C/T]CTGTGGCCAAAACAG	84708
rs540736737	snp	C/T	1.73423e-05	0.00294463	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461622	TAATCAGTGTACATG[C/T]ATATTTAAGTTTCAC	84708
rs540746170	snp	A/G	0.00159617	0.0282053	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53505807	AAAAGGGGGCTGAGG[A/G]AGTGAGGTTTCCAGG	84708
rs540790510	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53513127	TTTTAACTCAAAAAC[C/T]GCCCAGGGAAATGTT	84708
rs540813325	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53466407	CAGTCTACAGCTCCC[A/T]GCGTGAGTGATGCAG	84708
rs540836944	snp	A/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53488289	CTATTGCCTGCCTAT[A/T]GGTCTAGTTATGCCC	84708
rs540842981	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	LNX1, LOC101928879	GRCh38.p7	4:53577541	GAGATAGGAGGAAAC[C/T]AAGGGGGAGCTTTGC	84708
rs540849463	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53546139	TCAATACAAGCTAAA[G/T]CTTGTTAATGTTTCA	84708
rs540858893	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53527553	TTCTGGAGGGCAGGC[C/T]CCAGCCTCCTTTCAA	84708
rs540880615	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53484634	TATGGTTGTCTGACA[C/T]TAACCAGTCCAAATC	84708
rs540894357	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53495616	GGCACGATCTCAGCT[C/T]ACTGCAACCTCCGCC	84708
rs540910813	snp	C/G			intron-variant, missense	LNX1, LOC101928879	GRCh38.p7	4:53575735	GCTGTGGGGGCCACA[C/G]CTCTGTATTGCATCA	84708
rs540922165	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53534844	TCCAGACTGCTATGT[C/G]TGGGGACCTTGGCAT	84708
rs540936308	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53534139	GAGAAGCCTAGGGCC[A/C]AGTTACCCCATGGAG	84708
rs540952733	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53629061	GGGTGCACTAAAATA[C/T]CAGAATTTATCACTA	84708
rs540963982	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53544334	GAGTAGCTGGGACTA[C/T]AGGCGCATGCCACCA	84708
rs540977651	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53632002	ATTAATGTATGAATG[C/T]GGAGAAGGAGCGGCC	84708
rs541020428	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53483130	TGATTCATGGGGGTG[A/G]GTCTTTCCCATGCTG	84708
rs541022442	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53474957	ATTTTTAGTAGAGAT[G/T]CGGTTTTGCCATGTT	84708
rs541063288	in-del	-/AAGCACTTC	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53555374	CTGCCTCATTCCTCT[-/AAGCACTTC]AAGATCCAGCTTAAA	84708
rs541106850	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53547457	GCTAGAGGAGACTAT[A/G]TAGGAACTGGGGTCA	84708
rs541146188	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53539408	CTCACTCTGTCGCCC[A/G]CCTTGGAGTGCAGTG	84708
rs541160453	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53641459	AGGAATGGCTACAAC[C/T]TCTGTGCTCAGCCAA	84708
rs541166839	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53589670	AAGTAACTTGCTCAA[A/G]GATATAAATGAAGGA	84708
rs541174106	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53553562	AGAAAGATGAGAAGG[C/T]TGTTTCCATGCTCAT	84708
rs541213581	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53485276	GAAACTCCGATGTTT[C/T]GAAGGATCCCAGCAG	84708
rs541216634	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53567735	AAGGATCAACAAAAT[A/T]GATAGACTGCTAACA	84708
rs541226914	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53477386	GCCAGGCATGTAGTA[G/T]GCCTCCAGTAAATAT	84708
rs541253807	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53557786	TGTGGAATTTAAAAT[G/T]GATATATCAGCTAGG	84708
rs541256588	in-del	-/TTCAGTATT	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53539971	GGTTAGAACTGGAAA[-/TTCAGTATT]TTCAGTATTTTCAGT	84708
rs541264921	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53557811	GCTAGGGAATGGACT[C/T]GGGTCCCACCCCCAA	84708
rs541267316	snp	G/T	0.000798403	0.0199641	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53600576	ATTACCAGAGAGAAG[G/T]ACTCTCAGTCAGATT	84708
rs541282312	snp	C/T	0.00279162	0.0372561	intron-variant	LNX1	GRCh38.p7	4:53581685	ATCGCAAGAATAGCA[C/T]GGGAAAAACCCGCCC	84708
rs541289076	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53565372	CTAACTGGGAGGCAC[C/T]CTCCAGCAGGGGCAC	84708
rs541292568	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53483985	AGGTCATGAAGGCAG[A/G]TCCCTCCTAAGGGGA	84708
rs541293448	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519831	ACAAAGATTCACTTG[C/T]GCAGGTTTGCGCAGT	84708
rs541392731	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53573254	AGGTGGAATGGGGAA[C/T]TCGTGTTTAATGGAT	84708
rs541394225	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53641388	CAATAAGCTGATGAA[C/T]TTTTAATGAGTTTCT	84708
rs541396242	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53634470	GCTGGTCTCGAACTC[C/T]TGAGCTCAGGCAATC	84708
rs541400165	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53549563	TATTAAAGAATTATG[A/G]TTGTTTTTGGTGTGA	84708
rs541403802	snp	A/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53533233	AGGCACACGGAGACT[A/T]GCAAATGAAGAGAGG	84708
rs541431282	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53640902	TTTTATTTGGACAGT[C/G]TTTGTTTTTCTCAGT	84708
rs541446553	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53535078	TATGAATCCTCCTTG[C/T]TATAAGGAAAGAGAG	84708
rs541446649	snp	C/T			intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53499410	GTGATCCACCCACCT[C/T]GGCCTCCCAAAGTGC	84708
rs541507608	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53600938	CAAAATTTAGCCAGG[C/T]GTGGCAGTGGGCGCC	84708
rs541509913	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53571853	TTTTATAGAGATGGG[G/T]TCTTGCTATGTTGTC	84708
rs541516554	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53532599	ACAGCACTGCATTTT[C/G]ATAGTCCCCATAGGA	84708
rs541550065	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519257	CTTTTCTAGAGAAAG[C/T]ACCTTAGTCCAGGCA	84708
rs541590920	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53646961	AGAAGTGGAGGAAGC[C/T]GTAAAAGGCAGGAAG	84708
rs541599815	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53470196	TTCAACATATGCAAA[C/T]CAATAAACGTAATCC	84708
rs541600173	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53553192	GCATATAGCACTGAG[G/T]GGGGACACAGAGAGG	84708
rs541602135	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53612800	TGAGCTGGGAGGATT[A/G]CCTGAGTCCAGGAGT	84708
rs541605282	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53465797	TCACTAGTTATGAAA[C/T]ATAGTACCCTTTTTA	84708
rs541657231	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53581659	AACATATCTCATGAG[A/G]CTTACTCACTATCGC	84708
rs541660985	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53652133	TTTTTAAATTGTATG[A/G]GATTCTACCTGGTGG	84708
rs541700908	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53651705	CTCTCAACCTCTTTA[A/T]CCATGGGTAAAACTG	84708
rs541705825	snp	A/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53627015	CCCAGTTTGGTTTGG[A/T]TGGACAGGAGTGGGG	84708
rs541723920	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498348	GGGAATGAAGAGGAA[C/G]ATTGAAAAAGCTAGA	84708
rs541746902	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53470298	TTCAACAACCTTCAT[A/G]CTAAAAACTCTCAAT	84708
rs541755232	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53635027	TACGCAAGAAGTCTC[A/T]CTATGTTGCCCAGGC	84708
rs541765469	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53648642	TGTGCTTCCACTTTT[A/G]TCTCCTCTGGCTCTA	84708
rs541765644	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53546664	CAAGCTCTCCTTCGG[C/T]TCTCAAAAATTTATG	84708
rs541790525	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53633836	CCAGCTGTGGGACTT[C/T]GGGGAGATTGCATAA	84708
rs541814345	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53489966	GGGGACTTGAATGTT[G/T]ACAGTACCACAAAAG	84708
rs541858961	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53496790	GATTGCATTAAACAG[C/T]TCTTCAAGCCGAGTT	84708
rs541894879	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53593516	AAAACAGAAAGAAAA[C/T]AGAGAAATAAGAGTT	84708
rs541900233	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53628932	CTAAGCTATGGATAC[A/G]CAAGGGCATACAGAG	84708
rs541931019	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53591824	CTTTCCCCATATCTG[C/T]CCACAAAGGAGTTAA	84708
rs541940877	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53608895	TTCTCACTTATAAGT[A/G]GAAGCTAAATATTGA	84708
rs541951889	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53646285	GACCGGAGTGGAGTA[A/G]TAGGGCATGGTGGGG	84708
rs541952831	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53626047	CATGTAACAGAATGT[C/T]ATTCACCAATAAAAA	84708
rs541955904	snp	C/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53600215	ATAGAGTACTCTGTC[C/T]TCTAAGAGCCCAAAT	84708
rs541961380	snp	G/T			upstream-variant-2KB	LNX1	GRCh38.p7	4:53653297	TTTTCCCACTGGTTT[G/T]CTTAAGCACTTCTGT	84708
rs541962048	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53622165	ATATATTTAGTGTTT[C/T]CTAAGAAGGAAACTG	84708
rs541975667	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53650694	GCCTCTGCTGTGAAA[A/C]CTCTGTCCCCTTCCG	84708
rs541976550	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53559168	TACAGGATGAGACGA[A/G]TTGCAATGAACTGCG	84708
rs542005286	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53624078	GCCCTCCATGACTCC[C/T]TTTCTTGAGCTCTTT	84708
rs542012155	snp	C/T	0.00279162	0.0372561	intron-variant	LNX1	GRCh38.p7	4:53475573	CGTACTAAAACTAAA[C/T]GTCTCACTTTCATTT	84708
rs542038010	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53483863	TGGTGGTGGAGATAT[C/T]TTCTTCCTGCCTGCT	84708
rs542055457	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53518412	ACTCTCCTTTAATGC[C/T]GATGTTTTTCCTATC	84708
rs542083619	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53525806	AGGGAGGGCACTCTG[A/G]AGGCCAGGAAAGGGC	84708
rs542098347	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53613168	GAGGAAGCACCAAGC[C/T]AAAAAAGGAAAAGGA	84708
rs542098428	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53620833	GCTCACAGTGCAGCA[C/T]GCTCTAAATCAAGGT	84708
rs542102937	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53628362	TCTCAAAAAAAGTTA[C/T]ACAAATAGCCAAGAA	84708
rs542109970	snp	C/T	0.000296633	0.0121749	missense, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498696	GCGATCACCCCATCA[C/T]GATAAATGTGTTGGA	84708
rs542117827	snp	A/C	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53587404	GACACAGTCTTCCTT[A/C]CAAACAGTTTTGAAA	84708
rs542139089	in-del	-/C	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53614386	AAAGCCTCCAAGATT[-/C]TTCTGGAAATGGATA	84708
rs542146803	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53481937	ACAAAAACATCACTT[C/T]GATTATACCATTTTT	84708
rs542156489	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53594307	CCAGCTTGAGGGACC[C/T]CTCAAGAATGACCAG	84708
rs542164189	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53626768	CAAGGAAAGCTCCAG[A/G]GTTTCTTAAGGGTTT	84708
rs542172321	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53606742	ATCTAGCAGCAGATC[A/G]AAAAGCTTATCTACC	84708
rs542201264	in-del	-/AA	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53481605	TTAGTTTTACAAGTC[-/AA]AGTGTTTCTTTAAGT	84708
rs542205207	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53579334	CACCCTTTCCTTCTT[C/T]CTGATCTGGAATAGG	84708
rs542210001	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53538878	GAAGACCCTCAATAG[C/T]GACAACATGTTCTGT	84708
rs542212702	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53624045	AACTCCATCCTTTTG[C/T]TTGCCTCTCAGAGCT	84708
rs542236266	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53640341	TCTTTGGGAGAGCAT[C/T]CTTAGCTGTGGAACA	84708
rs542250862	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53583027	GTTACTGGGGGGAAA[A/G]TAATTGCCAAAGTTA	84708
rs542302528	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53633325	CACTATCCTCTTTGG[A/T]CCCCCATGCACAATA	84708
rs542321809	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53545712	AAAACCTGATTTAAG[C/G]ATGAGAGGCTTGAAG	84708
rs542331195	snp	C/T	0.00557542	0.0525036	intron-variant	LNX1	GRCh38.p7	4:53493192	CAGGCTGGTCTCGAA[C/T]TACTGACCTCATGAT	84708
rs542363465	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53469478	TAGCAGAAGGCAAGA[A/T]ATAACTAAGATCAGA	84708
rs542376747	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53640010	GAACAGCACTCCAGC[A/C]TGGGCAACAGAGTGA	84708
rs542413284	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53467810	AGAATAAAAAGAAAT[A/G]AACAAAGTCTCCAAG	84708
rs542433961	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53564836	GCCTCACTTGGGAAG[C/T]GCAAGGAGTCAGGGA	84708
rs542444460	snp	C/T	0.00636936	0.0560724	intron-variant	LNX1	GRCh38.p7	4:53564539	GGCAGAATAATTATT[C/T]CCCAGAGATGTCCAG	84708
rs542469759	snp	A/G	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53572410	TGAATTCACTGACAT[A/G]ATGAGCGTGGAAAAC	84708
rs542472642	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53514476	TGACGTCTCATATGG[C/T]GGCAGGCAAGAGGGC	84708
rs542474622	snp	A/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53472031	TACTATAAAGACACA[A/T]GCACACTTATGTTTA	84708
rs542493884	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53610442	AAATGCTGCGGTGGC[C/T]CAAGCCTGTAATCCC	84708
rs542512619	snp	A/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53532477	TATGAATAAATAAAA[A/T]AAAAAAAAGAAAGTA	84708
rs542522777	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53563310	TTATAAACAAAAGCT[A/G]TGACAAGACTCCCAT	84708
rs542542903	snp	C/T	0.000181197	0.00951659	missense	LNX1	GRCh38.p7	4:53478643	GCAAATCCCATTCTC[C/T]ATGTGATGCTCCCCC	84708
rs542608392	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53536076	GCATTTTACAGTACC[C/G]TGTAGCTGCTTTGCC	84708
rs542610113	snp	A/G	0.000889548	0.0210709	synonymous-codon	LNX1	GRCh38.p7	4:53476929	TAATGCCACTGCCTC[A/G]CTCCGGCTGACCTCT	84708
rs542614799	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53567565	TCTAAAATTGACACC[C/T]TAACATCACAATTAA	84708
rs542651089	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53467269	ACTCCAACAGACCTG[C/G]AGCTGAGGGTCCTGA	84708
rs542655255	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519074	CATAGGTCAGTGCAT[A/G]GGGGAGGTGGTTGTG	84708
rs542676348	snp	A/G	0.0418186	0.138422	intron-variant	LNX1	GRCh38.p7	4:53565674	ACGAGCTGAGAGAAG[A/G]AGGCTTCAGACGATC	84708
rs542686460	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53493325	TACTTGGCATGAGCT[C/T]GGGCCCTCTAGGGCA	84708
rs542707763	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53520527	CTTTGGGGAGGGGGA[A/G]CAGGCAATTTCCATG	84708
rs542715219	snp	A/T	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53534808	GTGCTCTTTCTCATT[A/T]CTATTCAGCCATATA	84708
rs542720580	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53542605	GGACAGAGGCAAGAG[A/G]AGGGAAAAAATAGGT	84708
rs542724918	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53535642	AATTCATTGATACAG[A/C]TGTGAATAAGATGTG	84708
rs542726767	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53521539	AAAGATAGCTGGTTC[C/T]TCATACCAAATATTT	84708
rs542741062	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53630422	AGTTCAGACAAGGTG[A/G]CCTTCTTGTTTCAGC	84708
rs542762883	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53472507	AAAAGAAGAAGAAGA[A/G]AGACACAAGGGATCC	84708
rs542771596	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53622731	AGCCCTAACACAGTG[C/T]AGTTGCTTGTGTTTA	84708
rs542773802	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53487556	TTATTCTATACACAC[A/C]CTTGAAAGGAGACTC	84708
rs542776214	snp	A/G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53637380	ATTAGAATCATAGGG[A/G/T]TCCATGGTGCAGCTC	84708
rs542790100	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53549612	ATTTCTTAAGAATCT[A/G]TCTTTAGAGATAGGT	84708
rs542797039	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	LNX1, FIP1L1	GRCh38.p7	4:53460346	TAGGAGGTATTCATC[A/G]GTGATGGTAACAAAT	84708
rs542802827	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53588941	TGACAAGGCCAATCA[C/T]ATCCAATGGGTCATG	84708
rs542807796	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53570107	GGAAGTCAGTGTGGC[A/G]ATTCCTCAGGGATCT	84708
rs542831275	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53562163	TGAGCCTAAAATAAG[A/T]CTCGCTCAGGATCAA	84708
rs542833258	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53555890	CTTGTAGAAGAGAAA[A/T]TTTTTAAGTGGTATA	84708
rs542838867	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53499821	CAAGGCCTAGTTGGT[A/G]GCCTTGAGCAGTTCA	84708
rs542850659	snp	A/C	0.000798403	0.0199641	nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53603558	AAGGATGATGCCCGG[A/C]ATCTGCTCAGCTTCT	84708
rs542858794	in-del	-/A	0.0189856	0.0955633	intron-variant	LNX1	GRCh38.p7	4:53470958	CCCCATCGAGCTACC[-/A]ATGACTTTCTTCACA	84708
rs542865540	snp	C/T	0.00478085	0.0486577	intron-variant	LNX1	GRCh38.p7	4:53555088	CAGGAATCCAAAGCT[C/T]GGATAAAGGGTGGAG	84708
rs542883457	in-del	-/AAA	0.0310518	0.120672	upstream-variant-2KB	LNX1	GRCh38.p7	4:53654296	CTTATCACATGAAAT[-/AAA]AAACCAAAATGTTGG	84708
rs542892875	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53467418	GAAAAACCAGAAACT[A/C]TAAAAATCAGAGCGC	84708
rs542902478	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	LNX1	GRCh38.p7	4:53654466	TTTTATTTCTCCTTT[C/T]TCATCTGCGAGCAAC	84708
rs542996975	in-del	-/T			intron-variant	LNX1	GRCh38.p7	4:53644096	ACTTCATTCTAGTGA[-/T]TAAAAAAAAGTAAAT	84708
rs542998270	snp	A/G			upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53593375	AGGCCTTGGGTGGGC[A/G]GGGGAAGGGTGTAGG	84708
rs543000357	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53648518	TAACCCCTTCTCAGA[G/T]AGATGATTTGCCAAT	84708
rs543026309	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53470828	CAAACCACTGCTCAA[G/T]GAAATAAAATAGGAT	84708
rs543047391	snp	C/T	0.00398564	0.0444627	intron-variant	LNX1	GRCh38.p7	4:53582302	CACTTGACAGAGACA[C/T]ACAGGTGAACAGTTT	84708
rs543081117	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53499340	ATTTTTACATTTTTT[A/G]TGGAGACGGAGTTTT	84708
rs543082195	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53588865	GAAGTGACCAGGGCC[A/C]TGGGCACACAACTGC	84708
rs543084902	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53595718	TCTTGACAGGGAAAT[C/T]TAAGGGGGGAAGGAG	84708
rs543120108	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53594993	CTGGGATTACAGGTG[C/T]GAGCCACTTGGTCCC	84708
rs543124921	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53615291	CTCCTTCAGCAAGGT[A/G]AGGCTGCTTCTCCCA	84708
rs543159178	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53614714	TACCTTTGGTCAGCC[C/T]ACGCTGTTTATGGCT	84708
rs543173075	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53616936	AGTCATTTATAAAAG[A/T]TCCCTGACTATAAAT	84708
rs543239244	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	LNX1	GRCh38.p7	4:53654301	CACATGAAATAAAAA[A/T]CCAAAATGTTGGAAA	84708
rs543241662	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53532058	CAAGCATCTATTCAG[C/T]CTTGCAATGAGAAAC	84708
rs543248683	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53521111	GTTTTTAGAATAACT[G/T]GAAAGGGTGGGTTTC	84708
rs543270425	snp	G/T	0.00119737	0.0244387	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53595087	ATTGGTGTTGGCTGG[G/T]GCCATTGGGGAATAT	84708
rs543309248	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53624014	GATGCTGGGTTTTCA[G/T]GTAACCCAAGCTCTT	84708
rs543322189	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53651812	ATGTCACATAAACCC[A/T]GTTACTGTTAGTGGG	84708
rs543347401	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53609371	TAATTAAAAAGAAAA[C/T]AGTACCAGAACAATA	84708
rs543367147	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53513876	ATAAGGTCCTTACAA[C/T]GATCTATACGGCCCT	84708
rs543378361	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53485300	CCAGCAGAGTGTCCA[C/T]AGGCTTGCAAATTGT	84708
rs543404776	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53476603	TTCAGTTACAAATGG[A/G]AAGAGAGAATTATTT	84708
rs543405523	snp	A/C	0.00557542	0.0525036	intron-variant	LNX1	GRCh38.p7	4:53565556	ATGGGGAAAAAACAG[A/C]ACAGAAAAACTGGAA	84708
rs543410675	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53629146	AATGTGAAAAACAGA[C/T]CACAAACAAAAAGTC	84708
rs543422855	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53505288	TTTTTTGAGATGGAG[C/T]CACCCAGGCTGGAGT	84708
rs543430260	snp	A/G	0.000399281	0.0141238	missense, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573909	CATCCACTTCCTCTG[A/G]ATAGCTGTAGAAGTG	84708
rs543439254	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53581742	TCCCTCCCACAACAT[A/G]TGGGGATTATGGAAG	84708
rs543468779	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53573310	AAAATTTCTAGAGAT[A/G]GATGGTGGTGATAGT	84708
rs543497533	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53587113	AACCTACTACATTTT[C/T]GGACAACTCTAATTC	84708
rs543530006	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53541198	AAATGGCAGGAATGC[A/G]TTCTGTGATTTCAGG	84708
rs543533122	snp	C/G			utr-variant-5-prime	LNX1	GRCh38.p7	4:53652314	CTATGCATGAAAACT[C/G]CTCCACCTTTGTACG	84708
rs543551585	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53533963	CTGGCAGCCAACTGA[C/T]ACATCAAGGTGCCAG	84708
rs543560671	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53585514	ACCTTACAGGAAAAC[A/G]ATCTAAGAAGGTGTC	84708
rs543564078	snp	A/G	0.00478085	0.0486577	intron-variant	LNX1	GRCh38.p7	4:53540252	GCCAGGCATGGGGGC[A/G]TGCACCTGTAGTCCC	84708
rs543571243	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53466781	GCAGCAAGGCTGGGG[A/G]AGGGGCGCCCGCCAT	84708
rs543575346	snp	A/G			intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461086	TTAGTATTTTAATTC[A/G]TTGCTGAAGTTAATG	84708
rs543583085	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53642533	CCACATACCCTGTAC[A/T]CTCTAAAGTCATATG	84708
rs543593090	snp	A/C	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53471538	GCGAAAGAAACTACC[A/C]TCAGAGTGAACAGGC	84708
rs543613510	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53551821	GCCTTGGCCTCTCAC[C/T]CTGCCTTATGACCCT	84708
rs543626044	snp	C/G	0.000798403	0.0199641	upstream-variant-2KB	LNX1	GRCh38.p7	4:53653798	TTCTGACTCTTTTTG[C/G]TTCTACCCCTAATCT	84708
rs543633091	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507247	TGGAAGGTGATCAGA[C/T]TGCGTCATCCCTGAA	84708
rs543635325	snp	A/C	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53569648	CAATGGCAACAAAAG[A/C]CAAAATTGAGAAATG	84708
rs543636703	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53529224	TAGGAGATAAGGGCA[C/T]TGGAGCTGGAGCTGG	84708
rs543674001	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53560554	TAATGAGGTATGAGT[A/G]GAAATTACTGGGTAA	84708
rs543695311	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53601182	TCAGTTTTATGAATA[C/T]GGAGGTTTAGGAGTT	84708
rs543698872	snp	A/C	0.00199481	0.0315187	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53513763	CCCAACAGTCTCCCA[A/C]GAGGAGTCTTGCTTC	84708
rs543699687	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LOC101928879	GRCh38.p7	4:53575411	TCTTGCGTAGAAAGT[C/T]AATAAATAGTTTTCA	84708
rs543700414	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53482667	CTCTGGAGATGCAGA[A/G]GCAGAGTAATATAAT	84708
rs543710976	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	LNX1	GRCh38.p7	4:53652731	CTCCTAAATAGGCAG[A/G]GGCTACTGACTGGAC	84708
rs543720252	in-del	-/C	0.00438332	0.0466095	upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53593465	ATGTTCACATACACA[-/C]CAGTCATCTACATAT	84708
rs543721696	in-del	-/G			intron-variant, utr-variant-3-prime	LNX1, LOC101928879	GRCh38.p7	4:53577152	TACTGGAATCTCACA[-/G]GAAATACTTTAAGTG	84708
rs543737371	snp	A/G	0.00953873	0.0683987	intron-variant	LNX1	GRCh38.p7	4:53567504	CAAAGCAGTGTGTAG[A/G]GGGAAATTTATAGCA	84708
rs543745198	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53470787	CAACTTACAAGGGAC[A/G]TGAAGGACCTCTTCA	84708
rs543758129	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53614597	AGGAAAATGACCAAT[C/T]GCTCTTAAGGTCATA	84708
rs543777516	snp	A/C	0.00358779	0.0422022	intron-variant, missense	LNX1, LOC101928879	GRCh38.p7	4:53576044	CCAACACCTTCAGGG[A/C]CCAGCTCCAGGAACT	84708
rs543784739	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53652165	GGAACCGGGCCATCT[C/T]ACCTTTGCTGTATTG	84708
rs543788403	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507627	TTTTTAAGTTTTCTA[C/T]AGTGAAATATGTACG	84708
rs543869981	snp	C/T	0.00358779	0.0422022	intron-variant	LNX1	GRCh38.p7	4:53570304	ATTAAGAAAATGTGG[C/T]ACATATACACCATGG	84708
rs543873409	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53526914	GTTTATAAAATTATA[C/G]AGCTAATTCTTCTTT	84708
rs543878810	snp	A/C	0.0103295	0.0711199	intron-variant	LNX1	GRCh38.p7	4:53472691	CAACAACAACAAAAA[A/C]AAAAAAAACAAAAAA	84708
rs543913068	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53537384	TCAAGTTCTAGTCTT[C/T]CCTCTGTCTAATCTA	84708
rs543946308	snp	C/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53595862	TACTTTGCCCATTTT[C/G]CTTCCTATTTTTTTT	84708
rs543982680	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53529950	AAAATGCTACAGAGA[C/T]TAGAAAAAATGTAGG	84708
rs544001706	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53479500	CATGAACCAGTGTCC[A/G]TGACCATTTCCTTTC	84708
rs544010701	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53642041	GTCTGGGCAACATAG[C/T]GGAGAACTCATCTCT	84708
rs544034435	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53619105	GGCTAGTGGCTACCT[C/T]ATCAGATAGTGTAAC	84708
rs544035806	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53506645	GGATCACCTGAGTTC[A/C]GGAGTTCGAGACTAG	84708
rs544046360	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53647782	CTCCCTTTCCCTCAG[C/T]CCCCGGCAACTGCCA	84708
rs544047897	snp	G/T	0.00199481	0.0315187	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53513149	GGAAATGTTCCCATC[G/T]CTTCCAGGCCTTCCC	84708
rs544074097	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53463411	GAGTATTTAACTTTA[C/T]TGCCGCAGCGAGAAC	84708
rs544083129	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53647046	AAGGTTCTCCATGCT[C/T]CATTTTTTCTCTTTT	84708
rs544114530	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53608215	ATATTTGTAAACTGT[G/T]CATCCTACAAATGTC	84708
rs544128275	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53510409	GAAAAGGAGTTTGGT[C/T]ATACAACCTTATGTC	84708
rs544129483	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53563565	TTTGAGACAGAGTCT[C/T]GCTCTGTCACCCAGG	84708
rs544130100	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53609045	CAAAACAGCGTGGTA[C/T]TGGTACAAAAACAGA	84708
rs544131911	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53490978	GTTTAGTAAGCAAAA[G/T]AATCTTTTAGGAAGT	84708
rs544139757	snp	A/T	0.00358779	0.0422022	intron-variant	LNX1	GRCh38.p7	4:53468556	GACTGGCAAACTGGA[A/T]AAAGTCAAGACCCAT	84708
rs544148689	snp	C/T	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53623646	GTAATTTTAGCCAAT[C/T]AAATTCTCAATTTGA	84708
rs544182417	in-del	-/AG	0.00199481	0.0315187	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53522526	ATTACATATTGACAC[-/AG]AGAGTTGCATGGATG	84708
rs544182631	in-del	-/ATGTCCTTTGTAGGGACATGG	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53472175	AAAAAGGATGAGTTC[-/ATGTCCTTTGTAGGGACATGG]ATGAAGCTGGAAACC	84708
rs544206972	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53643204	TGCCCAAGCTGGAGT[G/T]CAATGGCACGATCAT	84708
rs544221731	snp	C/T	0.00398564	0.0444627	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53602726	AAGGAATGAAAAACA[C/T]GTGTTGGGTGATAGT	84708
rs544230489	snp	A/C	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53522707	TTTTCTGATTTCAAA[A/C]GTAATTGAGGCTCAG	84708
rs544262500	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53584423	TGCAAGAGAATACAT[A/G]ATACATGGCAATGTG	84708
rs544267232	snp	A/T	1.70769e-05	0.00292202	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461604	AGCACCTGAAATAGA[A/T]TGTAATCAGTGTACA	84708
rs544297511	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53555835	AGATTGCTTGTGTCC[A/G]TTCAGTTATTCAGCA	84708
rs544313769	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53514671	GTGAGGACAGTCAAA[C/T]CATATCAGGGGTGAA	84708
rs544319312	snp	G/T	0.00716266	0.059414	intron-variant	LNX1	GRCh38.p7	4:53618699	AAGCCACATACAGAG[G/T]TTTAAATTTTCCAGT	84708
rs544323389	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53522203	AAACCCATCTCTACC[A/G]CAGGTCTTTGTCCAA	84708
rs544324475	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53625065	TAGGCACATTGTACA[C/T]ACAGATTAACTTGAA	84708
rs544338754	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53622108	ACACTAAGTTATATG[A/C]TTCTCTTATTTCCCT	84708
rs544403014	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53549003	AGGAAATGACCGACA[C/T]TGGGGTCTACTTGAA	84708
rs544413908	snp	A/G	1.64798e-05	0.00287047	intron-variant	LNX1	GRCh38.p7	4:53557867	CACGGACAGAGAGGG[A/G]ACTCACAGTTCTGAA	84708
rs544431165	snp	A/G	0.00358779	0.0422022	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53514873	GTTTAATGAGTTTTG[A/G]GTTATTGACCTCAAG	84708
rs544447607	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53624490	CCCCAGCCACATGCA[A/C]CTGTGAGTCCATTAA	84708
rs544451728	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53536837	TTATTTAAATAACAC[A/G]AAAGACATGGTAGAT	84708
rs544475922	snp	A/C	0.000798403	0.0199641	intron-variant, missense	LNX1, LOC101928879	GRCh38.p7	4:53576379	TGTGAGGGCAGCCTG[A/C]AGGACTGACCCCTCA	84708
rs544478755	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53605674	TATATAAGTGAAATC[A/G]CGCAGTATTTTTCTT	84708
rs544484422	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53631171	AGTTTTAGTACCCAG[G/T]GGGAGACAGTTTGTC	84708
rs544510352	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53578347	TTACACACACCTTCA[C/T]GGTATAGCTGACTAT	84708
rs544536919	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53637957	AAGAGAGAAGGCTCC[C/T]ACTGTGTATTCTTGA	84708
rs544550089	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53556299	AAAACTAGAAGAATG[A/C]AAGAAAGCATTCTCC	84708
rs544600312	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53570277	CCCAAATGTCCAACA[A/G]TGATAGACTGGATTA	84708
rs544603456	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53649855	TTCCTTGAGGGTGGT[G/T]ACTAAGGTTTTAAAT	84708
rs544604431	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53479417	AAGAGATGTTTAGTT[A/G]TGCACTGAGGGGCTG	84708
rs544620919	snp	C/G	0.000399281	0.0141238	intron-variant, missense	LNX1, LOC101928879	GRCh38.p7	4:53576236	GCTTCCTGCAGCCGA[C/G]GGTCCTGATGCAGCT	84708
rs544641502	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53617679	GTGCACTGTAAATGT[C/T]TCTCTTGTTTTGTTG	84708
rs544710001	snp	A/C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53474152	CTTATTTAACCAGTT[A/C/T]CTAATTGGCAGTGGA	84708
rs544716693	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53649865	GTGGTGACTAAGGTT[G/T]TAAATCTCTATGTTC	84708
rs544751340	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53486368	CTGGGGCTACAGGCA[C/T]GCCACTTCACCCAGC	84708
rs544755201	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53471879	TAGAAACACTTTTAC[A/C]CTGTTGGTGGGACTG	84708
rs544756970	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53467520	AGTTGAGAGAGGAAG[C/G]CTTCAGAAGATCACA	84708
rs544825981	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53494849	CAGCTTATGAAACGT[C/T]GCTGAGACACAAAAC	84708
rs544851607	snp	A/T	0.000399281	0.0141238	nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53605162	GGAGAAATAGATTCT[A/T]CCTCTGGATGGGGAC	84708
rs544888180	snp	C/T	0.000399281	0.0141238	nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53604252	TTAGCACCTAAAGCT[C/T]GTATATTCATTTATC	84708
rs544894704	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53590071	AGAGACAAGTGGTGG[C/T]CAAACCCCCCCCCTT	84708
rs544897889	snp	C/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53468259	GCTCTATAAGTGAAG[C/G]AGAAATAAAATACTT	84708
rs544929935	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53516032	GGGGTGGAAAGATCA[A/C]TTGAAGCCAGGAGTT	84708
rs544930363	snp	A/G	0.00478085	0.0486577	intron-variant	LNX1	GRCh38.p7	4:53550207	CTTCAAAATACACAA[A/G]TTTAAAAATTCAAGG	84708
rs544931605	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53589675	ACTTGCTCAAGGATA[A/T]AAATGAAGGAGATTG	84708
rs545009568	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53562265	TCTCCAGGGGCCCCA[C/G]TACACACTGGTAATG	84708
rs545020556	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53517731	AAAACCCATGTTGCC[C/T]GGCACTGAATTACAT	84708
rs545033510	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53467434	TAAAAATCAGAGCGC[C/T]TCTCCTCCTCCAAAG	84708
rs545055929	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53521647	TTTAAAAGAAACAAC[C/T]TTACTCCTTCTATAA	84708
rs545058453	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53494675	CACACTGGAGGATCC[C/T]TTGGAAGAATAATCT	84708
rs545084196	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53536750	CTTGACAAACCACTC[C/T]TTTGTTTTTCTATAA	84708
rs545085964	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53617120	ATATAAGAATCTTGG[C/T]TCTAAAGGGACTTAC	84708
rs545104428	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53514599	CATGGATCTCCAACC[G/T]GGTCCCTCCCACAAC	84708
rs545120432	snp	C/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53513522	GCAGCTCAAACTTAA[C/G]ACTTTCATCCTCCCT	84708
rs545129391	snp	C/T	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53491890	GCAACCTTCACCTCC[C/T]GGGTTCAAGTGATTC	84708
rs545157133	snp	C/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53511423	TTATGCTTCCTTTCA[C/G]TTACTCTGAGCACTA	84708
rs545202360	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53553954	GCATGTGGTTCGGAG[C/T]TCCAAGCTAAGGAAT	84708
rs545204386	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53644652	CTATTCCAGGAGGGA[A/G]CGGGATTCCATGTCA	84708
rs545209281	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53562989	GCCGAGACGGATCAC[A/G]AGGTCAGGAGATCGA	84708
rs545236934	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53650273	AGTAGGCACCTGTGC[G/T]GGGTGTGGAGGACAT	84708
rs545241675	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53542808	TCTGTATTCGGAACA[C/T]GTGACCCAGAGTGAT	84708
rs545243117	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53556613	GAAAAGCTTCTGCAA[A/G]GTCATTATTTCCTCA	84708
rs545255677	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53493725	AGTCAGTTACTGCTG[C/T]TGACTTACTGCCTAT	84708
rs545263335	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53588891	ACTGCTCATATGCAA[C/T]GACTCAAGGTCACCC	84708
rs545273975	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53649958	ATGGAGAACCTAGAC[A/G]AGGACTTGACAGAGA	84708
rs545283378	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53549697	AGTTAAAGGAGATAT[C/T]GATAAGATGGCCTTG	84708
rs545293150	snp	A/G	0.000207562	0.0101852	intron-variant, utr-variant-5-prime	LNX1	GRCh38.p7	4:53558012	CACCTTCTGTCAGCT[A/G]CAAGGGCCCAAACCA	84708
rs545300947	snp	A/G	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53589566	TGGATGCTAACATAT[A/G]TTAGCTACCTCATTT	84708
rs545312391	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53618591	CCCATCTCACTAACC[C/T]TCGGATGTGCACACT	84708
rs545343254	snp	C/T	0.00676609	0.0577691	intron-variant	LNX1	GRCh38.p7	4:53555785	GGTAATGGTGATTCC[C/T]GGCAAAGTATGATTC	84708
rs545343347	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53549191	AAAAAATAAGTTCTC[C/T]CCTTAAAGCTTCTGG	84708
rs545346578	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53561524	AGCCACTGTGCCTGG[A/C]CCTCCGTGTATTTTT	84708
rs545363120	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53642614	AGCTCTGGAAAGAAA[A/G]AGCATTTTCTGGGTG	84708
rs545381355	snp	A/C	0.000798403	0.0199641	utr-variant-3-prime, downstream-variant-500B	LNX1, FIP1L1	GRCh38.p7	4:53460418	TAGTGATAATACAAA[A/C]GTAATCTTAATTAGT	84708
rs545409554	snp	A/C	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53651562	TGTCAGAATACGTGG[A/C]CAAGAATGTACTCTG	84708
rs545416100	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53643144	TGTTGAGTCAAGAAA[C/T]CTTGGTCTTTTTTTT	84708
rs545424033	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53528338	GAAACAATTCATAAG[C/T]TACAGTTCAATAGTA	84708
rs545439628	snp	C/T	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53471422	TTACCATTCAGGACA[C/T]AGGCATGGACAAGGA	84708
rs545440619	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53513933	ACTTCCTCTCCATCC[C/G]TTGCTCATACAGCCC	84708
rs545441271	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53559124	TGATAGCAAACTCCA[C/T]TCCACAGGAAGTAGA	84708
rs545459918	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53640166	TAGGTTTTTAACATT[C/T]TTTTGTTCCCATTTC	84708
rs545461817	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53512143	CATTGGGGACCATGG[C/T]GAGCAGTGCTGCTTG	84708
rs545495245	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53609735	GTACAATATATAATA[G/T]ACTATTATATATTAT	84708
rs545503554	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53520543	CAGGCAATTTCCATG[A/C]GACAGATGATTTGAG	84708
rs545510487	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53553521	TCTACAAGTCTCTCC[A/C]CATGCAGGGCTGTAA	84708
rs545514872	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53525051	ATTGGACAAACAGTA[A/G]TGGTCTACATTGGAT	84708
rs545525801	snp	A/G	0.0111196	0.0737302	intron-variant	LNX1	GRCh38.p7	4:53568176	TCTGATACCAAAGCC[A/G]GGCAGAGACACAACC	84708
rs545528550	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53607069	AGGATGCCTTCTCTC[A/G]CCACTCCTATTCAAC	84708
rs545552006	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53477935	TATCTCTTGAACCTG[G/T]ACTTTTAAATGGCAT	84708
rs545552763	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53564052	AGAGCTGCTGTGGGC[A/G]CCTGTGAAGGACTCA	84708
rs545577204	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53590022	GCACTTTTATCAGAA[A/G]ATCCAAGCTTTGAAT	84708
rs545582975	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53630557	ATGGTGCTGAAGTGC[C/T]GCCTGGTGTTCCTAA	84708
rs545589139	snp	G/T	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53592491	CCATTGAAACGCTGC[G/T]TATTTTTACCACCTG	84708
rs545596373	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53517527	AGAATTCCTCTAGTC[C/T]TCAGGCATCCTGGTC	84708
rs545606155	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53605814	ATAATCTCTTTATCC[A/G]TCATCTATCAATGGA	84708
rs545647238	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53634917	ATCGTAGCTCACTGC[A/G]TGGGCTTAATTGATC	84708
rs545649107	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53578656	AATGGAATGGAGTAA[A/G]CAAAAATGGCAGATT	84708
rs545650658	snp	C/T	0.000232535	0.0107802	missense, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461522	TATTCTTCATAACCT[C/T]CTACAATGCAGAAGC	84708
rs545667438	snp	A/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53614878	GGAGGACTCCAGAGG[A/T]GTGGCCTGACCTCAG	84708
rs545672958	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508572	TGGTAATTCCTGCTT[A/G]CTGGTGTTTATTTTG	84708
rs545674475	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53546629	ATCTATAAAATAGGG[A/G]GATTAGACTAAATCA	84708
rs545674942	snp	A/G/T	0.00398731	0.0445001	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53499943	AATCTGCTTTCCCCA[A/G/T]GAAATCTCTCCTAGC	84708
rs545687590	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53595882	CTATTTTTTTTTCCC[A/G]TGACATATTTCTAGA	84708
rs545703950	snp	A/C	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53515184	TCCTCACATTAGTGC[A/C]AGAGAAGTGTTGGCT	84708
rs545730428	snp	G/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53467757	CGATGGAAGACAAAA[G/T]GAATGAAATGAAGCG	84708
rs545758100	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53625232	AATTGGTTTTCATCA[A/C]AATTAAATATTTTTG	84708
rs545761088	snp	C/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53601431	TGCCATGGGTATGCT[C/T]GCACCCCCACATTGG	84708
rs545762547	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53613214	ACACATAACTGTACA[A/C]ATGAACATATGTTTA	84708
rs545824728	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53511496	GATGAATACAAGGAA[C/T]ACAGAAAACCCCTTT	84708
rs545838118	snp	A/G	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53469428	ACATCACAATTAAAA[A/G]AACTAGAGAAGCAAG	84708
rs545851846	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53537552	ATGGACATTTTTTAT[C/G]TTCCTTTAGTATTTT	84708
rs545858670	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53598750	TTGAGTCATCTCTTC[G/T]TTTTCTTGAGAGTCA	84708
rs545864218	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53599800	CACCCGAGAAAACCT[A/G]TACCTCTTATAGCTT	84708
rs545868039	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53488337	TCAATTTCCCTGTGA[A/C]AATCCTATTTGAGGA	84708
rs545871093	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53609149	AGTTGACAAAAACAA[A/G]CAATGGGGAAAGGAC	84708
rs545882268	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53631937	TTGAAAATTTTAAGT[A/G]AAATCTGCTGAAGAA	84708
rs545901963	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53598120	TCCTCCATCTGCAGG[A/G]CTCAGCTCAGATACC	84708
rs545910905	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53584624	TGAGCAAATGTGTCA[A/G]TCAAGGAAGAGTAGT	84708
rs545934958	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53650779	CATGGTTCCAGAGCA[A/T]GCATCACACCTCATG	84708
rs545952752	snp	C/T	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53539626	CTAGTATAATGTGAG[C/T]ACATGATTCATATGA	84708
rs545956572	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53469038	TCAACAGAATATACA[C/T]TCTTTCCAGCACCAC	84708
rs545973129	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53580366	TCCAAATCTCTTCTG[C/G]AAGCTCCCCAATTTA	84708
rs545977663	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53650711	TCTGTCCCCTTCCGT[G/T]TCCCCCCAAGAACCT	84708
rs545987222	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53627583	TAAAGTGAATCCTGT[C/T]AAATGAAAGAAAAGA	84708
rs546012356	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53586750	ATTGTAAAAACTGCA[A/G]ATCTCAAATTGGTGG	84708
rs546019174	snp	C/T	0.00279162	0.0372561	intron-variant	LNX1	GRCh38.p7	4:53628888	GAATGGAAAACCAGA[C/T]ACTGCATGTTCTCAC	84708
rs546022676	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53524252	TTGTCAAAACTGTGG[C/T]GGATTTGAAGAGCTA	84708
rs546023284	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53638839	AGCCAAAAACAACAG[A/T]TGTTAGCAAAGTTGC	84708
rs546023922	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53497540	TGGCAGGGCCGGGTT[C/T]CCCCATCACCTCTGG	84708
rs546077932	snp	A/C	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53626483	CTCATTTGTTCATTT[A/C]CCAAGTCTTTGTTGA	84708
rs546084343	snp	C/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53504480	TTGTTTTTCTATCCA[C/G]GTTACTCAAACTTTC	84708
rs546098884	snp	C/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53600644	TCATTTGACTTTTCT[C/G]AAATCACGAGCATGT	84708
rs546115077	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53625783	CTGCACTCCAGCCTA[C/G]GTAACAGAGCAAGGT	84708
rs546121076	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53502172	CTGGCATTGAGCTAA[A/G]CTACTTGAATGCATT	84708
rs546122382	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53640820	TTCACAAAATTGTGC[A/G]TTGACTATTTCTCAC	84708
rs546127723	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53592557	CTGTGGATTCCCCGT[C/T]CCGGAAGATGGCCTG	84708
rs546143089	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53632727	ATATCAGGTTAGGGA[G/T]ATTTGGAATTATATT	84708
rs546161669	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53624296	AGTGGAAGGGATCTG[C/G]TGGGAGATAATTGGA	84708
rs546179798	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53639535	AAACAGAAACGTACA[A/T]TAAACAAGGTTATTT	84708
rs546188480	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53544928	GGAGTCCCGCTTGTG[A/G]TCATAATGCACTCGA	84708
rs546211336	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53557366	TTCTTCGTATCCCAT[A/G]GGTTTCAAAAGCATC	84708
rs546281501	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53463373	TTAATTAAAAAGTAA[A/G]CGCCTTCTTTTAGTG	84708
rs546301352	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53550552	GCTCACCCTGTTGGT[C/T]TGAACTTTGAAAGTG	84708
rs546326850	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53556807	TGGTCCAGCTAATTA[A/C]AAAGGAGGCACGGGC	84708
rs546338421	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53629260	TGGCTAAAGGTCCCT[C/T]CTCCCTGTCTCCAGC	84708
rs546357961	snp	C/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53644958	AGTGAGGGAGAAGTA[C/G]TACCTTAGCCCCAGC	84708
rs546358489	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53597620	TGAGCCAGAGCTTTC[A/G]TCTGTGGCTCCACAC	84708
rs546372798	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53607770	TACTGGTACAAAAAC[A/G]GACACATAGACCAAC	84708
rs546375934	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53481013	ATTTGGACTAAACAA[A/G]GTTTGTGTTGCTTAA	84708
rs546389584	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53481379	AGAAACCAGGCAAAC[C/T]GCTTGCTTCATTTCA	84708
rs546399121	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53572263	TAGACTACCCTACCC[A/T]CTCCTCCTTTAACCA	84708
rs546400156	snp	C/T			upstream-variant-2KB	LNX1	GRCh38.p7	4:53653643	TGATTGCCACTTTGT[C/T]CTTTTGACTTTCAGA	84708
rs546404404	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53638133	TATAGGTACAGATCT[G/T]GTCATTGGGCATATT	84708
rs546418947	snp	C/T	0	0	intron-variant, downstream-variant-500B	LNX1, LOC101928879	GRCh38.p7	4:53577950	TTTGAATATTTACCA[C/T]GCGCCAGGCACTGTG	84708
rs546418999	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53585113	ATCCTGTTTTGGTTT[A/G]GAGGACTCAGGATTC	84708
rs546419677	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53590476	TTCCTTTCTCTGACA[A/T]CAATATTGGCTAAAG	84708
rs546437863	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53579221	TTTAGAGTAAGAAAG[A/G]GTAGTGGAGTGGATT	84708
rs546452737	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53619053	ACTGCACTCGACCTC[A/C]CTTTAGTCACATTTC	84708
rs546457715	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53584814	ACACTTCCACTGATG[A/G]AGAACTGGTCAGTTT	84708
rs546465057	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53489175	TGGTAGCTCCTTCAA[G/T]GAGCTAAAAGCAATC	84708
rs546471777	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53531494	CACAGCTCCCTGGAT[C/G]AGACACACGGAAATA	84708
rs546483811	snp	A/C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53538274	CCACTGGACTGCCTA[A/C/G]AGAACAGTTGGGCAA	84708
rs546597164	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53638986	AATTCCATTACAGAT[A/G]TATATCCAAAAGAAA	84708
rs546597837	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53495308	AACAGTGACCCTGAC[A/G]AAGTCAACAAAATAC	84708
rs546601055	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53630640	CTTCCTTCAGGCACG[C/T]ATCACAGTGCTATTG	84708
rs546612689	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53598314	CACGGTTTACTGTAG[A/C]CTTGACCTCCTTATG	84708
rs546613967	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53486344	CTCCCGCCTCAGCAT[A/C]CAGAGTAGCTGGGGC	84708
rs546634037	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53638469	CATGCTCAAAGCAGC[A/G]AAACTTTAAGTCATG	84708
rs546640810	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53624309	TGGTGGGAGATAATT[G/T]GATCATGGGGGCAAT	84708
rs546650328	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53502493	AACGATCATCTGAGG[A/C]TTCAGCTTGTTGTAA	84708
rs546652545	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53510513	TTCCTGGCTTGAATT[C/T]GTGAGGTTTTACTGT	84708
rs546669063	snp	C/T	0.000399281	0.0141238	intron-variant, synonymous-codon	LNX1, LOC101928879	GRCh38.p7	4:53576081	CCCCCAAGACCTGGT[C/T]GGGGACTTGGCCAGC	84708
rs546682170	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53516142	AGCTACTCAGGAGGC[A/G]GAGGCAGGAGGACTG	84708
rs546732395	snp	A/G	0.000399281	0.0141238	nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53604680	TTCTTGCAACCAAAA[A/G]TGAATTATGAATATC	84708
rs546738458	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53630236	GTTACTCAGAATTGG[A/G]TATTTATACAGTCGA	84708
rs546788258	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53562562	GACAAGTATTGTTTA[C/T]AAATGAAACGCATTC	84708
rs546788721	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53538421	GCTCCCACTAACTCC[A/T]AGGAAAATTAGTGGA	84708
rs546810527	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53468425	GAGGCTAAGAAGAAA[C/T]TGCATCAACTAATGA	84708
rs546817662	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53632877	TCTCCAGGTCTTCTT[C/T]AGTAGGTTTCTTTCT	84708
rs546827308	in-del	-/AA	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53484611	ATCCACCAATGAAAC[-/AA]TATCCCTATGGTTGT	84708
rs546873901	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53467991	AGGAAATACAGAGAA[C/T]GCCACAAAGATAGTC	84708
rs546887890	snp	C/T	0.0107246	0.0724382	intron-variant	LNX1	GRCh38.p7	4:53472250	GGACAAAAAACCAAA[C/T]ACTGCATATTCTCAC	84708
rs546891306	snp	C/G	0.00318978	0.0398085	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53499798	CTGATTCATGATCAA[C/G]AAGAGGCCAAGGCCT	84708
rs546936596	in-del	-/T	0.00517822	0.0506191	intron-variant	LNX1	GRCh38.p7	4:53578887	TGACTGAACAAGCAG[-/T]TTTGGCTCTAAGGGA	84708
rs546954424	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53528550	ATTGTTAATCTCTTC[A/C]TGTGCCTAATTTATT	84708
rs546960190	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53533647	TCGAGTGATCCGCCC[G/T]CCTCGGCCTCCCAAA	84708
rs546970559	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53623086	TGGTGGGCTGATGTC[A/G]TCACTCAGGATTCAT	84708
rs546990685	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53627785	TCTATTGACTTTACT[A/G]CTCCTAAAAGACGGT	84708
rs547002625	snp	G/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53617358	AAGATGGTTCAATAG[G/T]CCAGACTAACCTGTG	84708
rs547033462	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53501620	AGAAATGCTGAAGCT[C/T]AGAGCATTAAGCAAC	84708
rs547048465	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53497806	GTATTTCTGTGAAAA[C/T]TGCTTTAGGTTATTT	84708
rs547066311	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53470457	CCCTCTCTCACCACT[C/T]CTATTCAACATAGTG	84708
rs547072238	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53596616	TGGCTGTTGCTATTT[C/T]GAAGGTTGCCATGTC	84708
rs547143338	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53587104	CCAAAAGGCAACCTA[C/T]TACATTTTCGGACAA	84708
rs547168495	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53472895	CTGGAAAAGGCTAAG[A/G]TGAAATAACCCTACC	84708
rs547169001	snp	G/T	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53611401	TTAAATTCTACAAAT[G/T]GATTATGTGTGTGGT	84708
rs547182839	snp	C/G	0.0260105	0.111035	intron-variant	LNX1	GRCh38.p7	4:53570528	GTGGGGTGGGGGGAG[C/G]GGGGAGGGATAGCAT	84708
rs547183639	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53647341	TTTTATTTCTGCATA[A/G]TATAATATTAATCTT	84708
rs547223451	snp	A/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	LNX1, LOC101928879	GRCh38.p7	4:53576564	TTCTTCTGCCTTAAA[A/T]CCCTGACTTCACAGA	84708
rs547236609	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53521271	TATGCAACCCCAGGG[A/G]CTCTGCAGAGGTTGT	84708
rs547297199	snp	A/G	0.00676609	0.0577691	intron-variant	LNX1	GRCh38.p7	4:53526497	ACCCTTGGCCAAGCA[A/G]CTGGTAAAGATAAAG	84708
rs547303554	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53610817	TTAAATTACTGAAAT[A/G]GAAGGCAAAATAAGT	84708
rs547309326	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519982	ATAAGTGACAGAGAC[A/G]GAATTTAAGTCAAGA	84708
rs547343424	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53621433	TTTTTCTCTGTAATT[C/T]GCAGGATTCAAAACC	84708
rs547395433	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53474484	CTATCAGGCCCTTTT[A/T]AGAAAAGATTTGCCA	84708
rs547408624	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573472	CAAATGCTATTTCCT[C/T]ACACTGAATCATGAC	84708
rs547460285	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53481550	TTGGATGGGAGACAC[A/C]TGTTATCTCTCCAAG	84708
rs547463265	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53645249	TCTCGGGAGGCTGGA[G/T]CCATGACAGAGCTCC	84708
rs547476555	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53535830	CTGTTGGCACAGTTC[A/G]TGAGCATGTCGGGCT	84708
rs547484144	snp	A/T			intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461135	GCTAGATTTTGCTAC[A/T]TCTGACCATTTTAAT	84708
rs547488914	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53534249	CTTTGTTGGTTTGGC[C/T]CTTAAAGGGTCTCTG	84708
rs547489568	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53497111	CTCTTTTATTGAAAG[A/G]CTAGATCTCTTTATA	84708
rs547493483	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53551471	ATGCGCACTAAGAGG[C/T]AAAATGGCAGAGTTT	84708
rs547514190	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53539138	CGTGTAATCACCCTG[C/T]TACAATAAAAGGAGC	84708
rs547518859	snp	A/C			intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461051	ACCACATCTAAAAAA[A/C]AAAACAAAACAAGAT	84708
rs547541175	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53628023	TATCGGTTTACAACA[C/G]TCCAACTTGAAGGCA	84708
rs547558833	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53651786	TGTGTTTTAAATGAC[A/G]ATAAAGAATAATGTC	84708
rs547575251	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53608560	GCAGTGTGGAGATTT[C/T]TCACAGAATTCAAAG	84708
rs547580270	snp	A/G	0.0248432	0.108648	intron-variant	LNX1	GRCh38.p7	4:53470431	TTGAAAACTGGCACA[A/G]GACAGGGATGCCCTC	84708
rs547592552	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53502485	TGCTGTTTAACGATC[A/G]TCTGAGGCTTCAGCT	84708
rs547611317	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53470889	TGGGTAGGAAGAATC[A/G]ATTATCATGAAAATG	84708
rs547618190	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53504907	CAATTACAATAGTAA[C/T]GCCAAAGATAACTGA	84708
rs547679203	snp	C/T	0.0023933	0.0345097	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53511755	AATGAGAGTTGGAGA[C/T]GAGACACAGGAGGGA	84708
rs547679280	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53504222	GCTGCAGCTTCTACA[A/G]TCAGCATTTGCTGCT	84708
rs547699772	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53606625	TTTGGTATCATCCTG[A/G]TATCAAAACCTGGCA	84708
rs547708481	snp	C/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53596709	TTTAAAATGTCTCTT[C/T]TCCTTGTTAACTTTG	84708
rs547711312	snp	A/C	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53607920	GCTAGCCAGATGCGG[A/C]AGATTGAAACAGTAC	84708
rs547717181	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53552074	ATGAATATTGTTCCT[A/G]GTGATTCCACTTACA	84708
rs547738761	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53517868	GCTGGGCAAGTCCAC[C/T]ATCTGGTATTCAGTG	84708
rs547749487	in-del	-/AAG	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53539280	CCTTCTCACTATAAA[-/AAG]AATAGTGAAGTATAC	84708
rs547753539	in-del	-/T			intron-variant	LNX1	GRCh38.p7	4:53586056	TAGAAAATGTATTAA[-/T]TTCCCTTTAATTCAT	84708
rs547765605	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53469204	CTCAAAACTGCTCAA[C/T]TACATGGAAACTGAA	84708
rs547768768	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53503417	GCTGCAGAATGGATA[C/T]TGTGTTATCAGGCAT	84708
rs547780743	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53518701	CTGGTAAGTGGAAGG[A/G]CTAGGATTTAAACTG	84708
rs547781856	snp	A/G			upstream-variant-2KB	LNX1	GRCh38.p7	4:53653356	ATTTTACTTAAATAA[A/G]CGATTAGCTCTGGGA	84708
rs547800801	snp	C/T	0.00438332	0.0466095	intron-variant	LNX1	GRCh38.p7	4:53538606	TTAGATTGCTTAAAC[C/T]TAGTATCATGGCATG	84708
rs547810040	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	LNX1	GRCh38.p7	4:53558181	GAGGATGTAGGAACG[C/T]AAGGAGCCACCACGG	84708
rs547810748	snp	A/C	0.0138799	0.0821421	intron-variant	LNX1	GRCh38.p7	4:53469753	TAGAAGAAATGGATA[A/C]ATTCCTCGACACATA	84708
rs547842230	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53650946	GTTGTTATGCACCAG[A/G]AAAGACTTCACATGC	84708
rs547864062	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53524601	AACAGGTCTGTAATG[C/T]TTTAAGCCTACGCTC	84708
rs547869220	snp	A/G/T			intron-variant	LNX1	GRCh38.p7	4:53547118	TTATATCAAATCGAA[A/G/T]ACTATGTCTATTGTG	84708
rs547902227	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53494210	AGTAAGTCTCACAAG[A/T]TCCAATGGTTTTATA	84708
rs547906980	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53619836	CACCCAGCAGCAATG[C/T]ATGAAGTTTCTGTTT	84708
rs547952741	snp	A/T	0.000798403	0.0199641	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53605639	TGTTTCTCTGTATTC[A/T]TGTTTTTTTTAAAAT	84708
rs547984072	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53599876	AGACTATGTATATTT[C/G]AGATATGGTCTCAGT	84708
rs547991188	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53476158	AAAAATGAGCTGGGC[A/G]TGGTGGTGTGTGCCT	84708
rs548011279	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53592788	GAGAGGGAAGAAAAG[G/T]AAGTCCGGATTCCCA	84708
rs548019512	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53645786	ATCAGGCATGTTGGC[A/C]TCTGTAGAACCTGTG	84708
rs548026993	snp	A/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53633003	GACATCATTAGTGTG[A/T]GAGTGGTGGGGAGTT	84708
rs548034872	snp	A/C	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53552674	TCTCTACTAAAAATA[A/C]AAAAATTAGCCAGAC	84708
rs548044985	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53526360	TTCATAATCTTGAAT[C/T]CTCATGTCTGAATTA	84708
rs548076019	snp	A/C	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53475913	AAGGAGAGATGATCT[A/C]AGAAATGTCTCCAAA	84708
rs548085793	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53464815	AAGTGATAATTTAAC[C/T]TCAAAATTTGTCTTT	84708
rs548106756	snp	C/T	0.00398564	0.0444627	intron-variant	LNX1	GRCh38.p7	4:53633048	CATAAACTTTGGGAT[C/T]GGAAATGTCTGGGTT	84708
rs548132201	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53612215	AGATTGTCTAAAATT[A/G]TAAAGATTTGTAACA	84708
rs548152985	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53610242	GATCATAATTCAATA[A/C]ATAAGAAAAAATTAT	84708
rs548178746	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53621282	CCCTGTGCAGTGCCC[G/T]CTGCCTGGGATGCCC	84708
rs548192284	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53524241	TGGTCATTATCTTGT[A/C]AAAACTGTGGTGGAT	84708
rs548192867	snp	C/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53490202	ATTGGCTCTAGAAAT[C/G]GCTTTGAGTATTTTC	84708
rs548222180	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53627677	CATGTGCTTAGAGAT[A/G]GGCCAGTCTTGAGTC	84708
rs548234210	snp	A/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53586246	AAAACACATGGTGAC[A/T]CATGTATTCATGCGA	84708
rs548243358	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53488402	TCCAGGTCAACTATT[C/T]CTAGTTTTTTCCACA	84708
rs548252261	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53581281	TAAGGAAGTTGAAAA[A/G]TGTGGAAAACATGAA	84708
rs548259127	in-del	-/TTTTTA	0.0309932	0.120565	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53600716	GCCTCTGTTTTTTTA[-/TTTTTA]TTTTTATTTTTATTT	84708
rs548267946	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53619046	GTGAGCCACTGCACT[C/T]GACCTCACTTTAGTC	84708
rs548286934	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53650477	CCGGCTTCTGATGAA[C/T]GTCAGAGAAGGGAGT	84708
rs548287454	snp	A/G	0.00438332	0.0466095	intron-variant	LNX1	GRCh38.p7	4:53561929	GTGTATCCCAGAATT[A/G]AAAAAAAGGAAAAAG	84708
rs548288573	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53504134	AGCGAGCGAGACTCC[A/G]TCTCAAAAAAAAAAG	84708
rs548290622	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53571762	AACTCCCAGGCTCAA[A/G]CAATCCTCCCACCTT	84708
rs548331402	snp	G/T	0.00557542	0.0525036	intron-variant	LNX1	GRCh38.p7	4:53624762	TGCAGGCCATCTACC[G/T]CCTGGAGCACTGCAC	84708
rs548360282	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53469967	ATCAATAGAAAAAGA[C/G]GGAATCCTCCCTAAC	84708
rs548361548	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53639836	CAGGGATTTGAGACC[C/T]GCCTGAGCAACATGG	84708
rs548391079	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53649047	TTATGGTGCCTGTAA[C/T]CCAAAATATATCAAA	84708
rs548411337	snp	A/T	0.00199481	0.0315187	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53511115	TGGGGAGGGTGCAGA[A/T]TCTTGATTTAAGTAT	84708
rs548453639	in-del	-/TTT	0.494774	0.0508504	intron-variant	LNX1	GRCh38.p7	4:53545803	ACTTCAGAGGCCACA[-/TTT]TTTTTTTTTTTTTTT	84708
rs548472003	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53517595	AGTTTGGATAATTAC[A/G]TTCTACGTGTCACCT	84708
rs548483663	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53516954	TCAATCCAAAGTGAA[C/T]TGCTGCCCCTGCCTG	84708
rs548489548	snp	C/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53612703	TGCCAGCTAATTTTT[C/G]TATTTTTTTTTTTTG	84708
rs548491203	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53620601	GCTTGATGGGTACAA[C/T]GTGCATTGCTCCACT	84708
rs548512748	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53474370	TTTATTGGAACACAG[C/T]CTTCCTCATTCATTC	84708
rs548566897	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53557468	TCAGGTATAGAGACT[C/G]TCTCAATAAAGGGAC	84708
rs548568640	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53550324	ATCTTGTTCCTGTTG[C/G]AATATGATTTCTCCA	84708
rs548578775	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53563356	CCTGGAGGCCTCACA[A/G]AGAAAAGTAAACACT	84708
rs548601938	snp	A/C	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53524455	ACTCTCTCCATTTGA[A/C]AGATAAGAAAATAGA	84708
rs548618923	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53605557	CTCTATATAACTACA[A/G]CTTTGTATCCTTGGC	84708
rs548625241	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53540754	AGACTGTGTAGACAT[C/T]GACACAGTGCTGATT	84708
rs548641683	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53530946	AGGCAGGAGGTATTG[C/T]TTGAGCTCAGGGGTT	84708
rs548668368	snp	C/T	0.00199481	0.0315187	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53520726	CAACACTTTGGGAGG[C/T]TAAGGTGGGTGGATC	84708
rs548672068	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53584716	AGTCATAGGATTTTG[A/G]TCGGTTAAGGAACTT	84708
rs548672527	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53497748	GCGGCCTGCCCCGAG[A/G]GCCCTGTCTTATGCT	84708
rs548696691	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53471265	CTATTTAATAAATGG[G/T]GCTGGGAAAACTGGC	84708
rs548700615	snp	C/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53601532	CTGTTCGCGTTCTGG[C/T]CACCTGCCCATAAAC	84708
rs548713916	snp	A/C	0.0103295	0.0711199	intron-variant	LNX1	GRCh38.p7	4:53567908	TAGAAGAAATGGATA[A/C]ATTCCTTGACACATA	84708
rs548737450	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53537676	GCCCCACACAGGTGG[A/G]TGGCCCCGGGCACCT	84708
rs548744364	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53637071	GTTTCACTCTCCTGT[C/T]ACTGCTAAGAGCATA	84708
rs548755114	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53575079	TGCCACCTCCCAGAT[C/G]CAAGTGATTCTCCTG	84708
rs548766860	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	LNX1	GRCh38.p7	4:53558114	TTCAGATTAAGCCAC[A/G]TTAATAAATCACGGG	84708
rs548781554	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53587891	GCAGCCACTCTACCC[G/T]GGAACTCCAAGAGAA	84708
rs548782815	in-del	-/C	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53632603	TAGTTGAGGCTGTAT[-/C]TTTGCTTGGAATTTT	84708
rs548787019	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53513671	ATCCAACATGAAATA[C/T]TCAGAATCCAACTAC	84708
rs548787071	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53482310	ACTGCAGGAAGAGAA[A/G]TCCTGAGCCTGACAC	84708
rs548787486	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53645114	GAAAGTTTGGCTTAA[C/G]TCTATTTTTGCCTGT	84708
rs548798584	snp	C/G/T	3.33485e-05	0.0040833	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508244	TGTAACAGAACCAGC[C/G/T]GGGAGGTGAAGAAGA	84708
rs548805779	snp	C/G	0.00597247	0.0543191	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53599056	TCTAACTTTAAGGCT[C/G]CAAGTTATTATAAAG	84708
rs548820305	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53650744	ACCCTAACTCACACA[C/G]ACTTAAAGGATTCCA	84708
rs548832089	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53463778	CCACTGAAATGAGTT[A/G]ATAAGTATGCTGAAG	84708
rs548832708	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53622953	TTTAATGAGTGAATA[C/T]AGTTGCACAAGAAAG	84708
rs548842534	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53606006	ACCCTTGCCAATTCT[C/T]ATCATTCCTTGTCTT	84708
rs548845056	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53611909	GTATTTGACTGAAAA[C/T]AGTATAACTTTTCAG	84708
rs548850050	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53511768	GACGAGACACAGGAG[A/G]GAACTCAGATGTGAT	84708
rs548862005	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53514801	CACCATACCATCTCT[A/G]TACTCAGACTTTTCA	84708
rs548864599	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53563861	ATTCTTAATCCTTGC[A/C]AATAAAATGTCAAGG	84708
rs548865391	snp	C/T	0.00279162	0.0372561	intron-variant	LNX1	GRCh38.p7	4:53549430	GCTCCTTTGTATCGG[C/T]GGAGAATGAAGAACG	84708
rs548874091	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53514251	AAGACAATGACTGGC[A/G]TATAGAAGGTGCTCA	84708
rs548878540	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53609834	AAAATTTCTACATAA[A/T]GCTATATAAATAAAT	84708
rs548898540	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53472424	GCACACCAGCATGGC[A/G]CATGTATACATATGT	84708
rs548920669	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53642734	GCCTGCGGGGTCTGA[A/G]GTTTCCTTTGGGTTG	84708
rs548929457	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53468729	AAACCAACAAAGATC[A/G]AAAGAGACAAAGAAG	84708
rs548959566	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53648897	ATGACAATCACTATT[G/T]CCCTGAAACCCACTG	84708
rs548962327	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53562712	AGATTATTTGTACAA[C/T]GAGGTGATTATAGTT	84708
rs548963222	snp	A/G	0.0551013	0.156571	intron-variant	LNX1	GRCh38.p7	4:53568446	TGATAAAATTCAACA[A/G]CCTTTCATGCTAAAA	84708
rs548966799	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53488401	TTCCAGGTCAACTAT[G/T]CCTAGTTTTTTCCAC	84708
rs548981055	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53468050	ATTGTCAGATTCACC[A/G]AAGTTGAAATGAAGG	84708
rs548982080	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53602846	TTTAAAACAAGCCAA[A/G]TATACCTGAAAGCAT	84708
rs548990774	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	LNX1	GRCh38.p7	4:53653847	AGTTAGCTCTCTTGT[A/G]TCATGGCGGTTACCC	84708
rs548993892	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53640231	AAAAACAAGAACGAC[G/T]GTCAGGAAGGCGAGG	84708
rs549029439	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	LNX1	GRCh38.p7	4:53653385	GAATCAGATTCTAAG[C/T]GGAAACATGAATAAT	84708
rs549047434	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53509138	AGGCTAGGTTTTGGT[C/T]AGGAAATGGTGATTT	84708
rs549054043	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53611767	GAATGAAAAATATAA[A/T]AGGTAAAGTAAACCA	84708
rs549098131	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53553950	ACCTGCATGTGGTTC[A/G]GAGTTCCAAGCTAAG	84708
rs549132755	snp	G/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53647163	GTTTCTCTAAATTTT[G/T]TGTGCAGAACTAGAC	84708
rs549142184	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53535029	TTAAGTCATGAAGCT[A/G]ATGGGAGATGTTTGT	84708
rs549147488	snp	A/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53643423	CCAAAGTGCTGGGAT[A/T]ACAGGGCTGAGACAC	84708
rs549151398	snp	A/C	0.0111196	0.0737302	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53601351	GAAGTGGCATGGTCC[A/C]CCCCTCTCCCACTTT	84708
rs549167532	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime	LNX1	GRCh38.p7	4:53652256	CTGGCTTAGCAGTAG[C/T]TCGGAAAATTTTTCT	84708
rs549180231	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53467561	CTAAAGGAGGAAGTT[C/T]GAACCAATGGCAAAG	84708
rs549192942	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460797	TACTTTTCCTGACAT[G/T]TTTACAATGTATTCT	84708
rs549228391	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53587687	GTAGTCAAGATCCCA[A/C]CAGACCCTATTTTCT	84708
rs549241234	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53470410	CAAAAACTGGAAGCA[C/T]TCACTTTGAAAACTG	84708
rs549268463	snp	G/T	0.00358779	0.0422022	utr-variant-3-prime, downstream-variant-500B	LNX1, FIP1L1	GRCh38.p7	4:53460289	TAAAAACAAAACAAG[G/T]TTATAATTAATTCTC	84708
rs549284177	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53629258	GGTGGCTAAAGGTCC[C/T]TCCTCCCTGTCTCCA	84708
rs549348193	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53547098	TAAAGTTAGTTGTTA[C/T]CAAATTATATCAAAT	84708
rs549373274	snp	A/G	0.00279162	0.0372561	intron-variant	LNX1	GRCh38.p7	4:53622338	GTGCGTGGATTAGAA[A/G]TACTGACAATTTTCA	84708
rs549383729	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53641622	ATATATGCCCATGAA[A/C]TCATCACTGCAATCA	84708
rs549393042	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53506066	TGAGGGCATAATACA[C/T]ACAGTGGTTTGGGTT	84708
rs549409088	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53491121	TTCCAAATGACATGA[C/T]GAGTAAGAGTTTTTC	84708
rs549422359	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53641133	CACTGGAATGTGGCA[C/T]GGTTTTTTGGCCTGG	84708
rs549480224	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53608287	TAAAAAACAACCACA[C/T]TAAAAAGTAGGCAAA	84708
rs549485874	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53526996	AAGGGTGAGGAATAC[A/T]TAAGAGGCTAAATAT	84708
rs549494926	in-del	-/C	0.00119737	0.0244387	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53517921	GCTGAATGGCCCTCG[-/C]CCCAGAGGACAGGTG	84708
rs549495704	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53621767	GGCTTCTCAGACCCC[A/C]CCTCAAATGATAGAG	84708
rs549496464	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53512609	CAAAAATGAGACTAA[C/T]TTTTCAACTGTATTT	84708
rs549512351	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53484097	GAGGAAGTAGCCATC[C/T]CCAGACACCAAACCG	84708
rs549544020	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53574267	CCCCATGGCCTCCTC[A/G]TGCCTCTGTTTTTCC	84708
rs549546714	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53642178	AGTGAGCCATGATCA[C/T]ATTACTGCACTCCAG	84708
rs549548569	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53648837	TGCAGAATTGCTTTA[A/G]TGATAATTGAATTTC	84708
rs549553875	snp	A/C	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53541302	GCTCTCTAAAACTAC[A/C]CTGACTTGGCAAGAT	84708
rs549564848	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53628770	AAAACCGTGGTACAA[A/G]TATACCCTGAAATAC	84708
rs549582022	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53581303	AAACATGAAGAGTAG[A/G]TATATCAAAACTTAA	84708
rs549620593	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53528692	ATAAGGGGGGGACTA[C/T]TGTATAGCCTAGACA	84708
rs549663389	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53520580	GTTATCTGTCCATGC[A/G]TTCAAGTGTGTATGT	84708
rs549667846	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53602171	AATGAAGTTACTCTC[C/T]GAAGTGATAAGGGGA	84708
rs549674851	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498153	TACTTTTATTTTCAG[A/G]GAGGGCCGTAAGACT	84708
rs549695902	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53615403	TATTCAAGAGGCTTC[A/G]CAGCTTCCACCCTTG	84708
rs549702741	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53554620	GCACTTTGGGAGGCC[A/C]AGGTGGGTGGATCAC	84708
rs549702789	in-del	-/T	0.00119737	0.0244387	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508806	TGGTCTGGGAGGGCC[-/T]CCCTGGTGTTGGGGG	84708
rs549714432	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53470334	AGGTATTGATGGGAC[A/G]TATCTCAAAATAATA	84708
rs549750492	snp	A/C	0.000399281	0.0141238	utr-variant-5-prime	LNX1	GRCh38.p7	4:53652358	CTGGGCATCCCCTGC[A/C]CCTTCTGCAAGGCTT	84708
rs549768534	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	LNX1	GRCh38.p7	4:53653171	TTATCACTCCCATTA[C/T]ATAGATAAAGAAACT	84708
rs549781695	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53566122	AGCAAGGCAGGCCAA[C/T]GTTCAGATTCAGGAA	84708
rs549785466	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53554686	GTGAAACCCCTTCTC[A/T]ACTAAAAATACAAAA	84708
rs549836935	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53574166	AGACATGAGACAGGG[C/T]TGCCAATGCATGGGG	84708
rs549858799	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53580749	TCAGTGGCTAAATAG[G/T]TCAGTACTGGAACTC	84708
rs549864649	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53607553	AAAGCAGTTTACAGA[C/T]TCAATGTTATTCCTA	84708
rs549880802	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53533811	CAGCCCCCACAACCA[A/G]GAATTATCTGGTCCA	84708
rs549888456	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53475062	CATGAGCCACCACAC[C/T]CAGCCCAGACTACTT	84708
rs549899505	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53559461	CTTGAGGTTAGAGTT[C/G]TAGCTCTGCTGCATA	84708
rs549911243	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53555717	CTCTCACAAAGCATA[C/G]ACAGCAATTGGAAGC	84708
rs549929793	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53651778	TGTGTGAATGTGTTT[A/T]AAATGACGATAAAGA	84708
rs549989814	snp	A/G			intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461801	TTTCCATAATTTTGA[A/G]TATCCTTAAAAAACT	84708
rs550000453	snp	A/G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53497949	AAATATACGAGCAGG[A/G/T]AGGGGTTTCTTGGCA	84708
rs550003443	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53613814	TTTATATTCCTTTGG[A/G]TATATACCCAGTAAT	84708
rs550015477	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53560229	CATATTGGTATTGGA[C/T]TGTATTTCTGACGAT	84708
rs550016266	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53466623	CGGCACCTGGAAAAT[C/T]GGGTCACTTCCACCC	84708
rs550037698	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53513396	TCAGAGGTGGAGCTA[C/G]ACTCTGAAGCCAGGC	84708
rs550062126	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53527708	GTGGTAAAGCTCATA[C/T]TCACACATCCAAATT	84708
rs550074596	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53477550	TGTGCAGGATCATTT[C/T]CATATAGATCATATA	84708
rs550080410	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53600609	GACTAACAGGGTCTC[A/T]ATATAATAATAGGGG	84708
rs550082745	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53608642	AATATAAATTTTTCT[A/G]CCACAAAGACATGCA	84708
rs550083236	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53533289	GATTTGCCCGAGGAG[A/C]TTGGTAAAAATAGAA	84708
rs550083995	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53550071	TGCTAATTCTCAAAG[A/G]GGGGAAAAAATAAAA	84708
rs550113024	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53468308	GAGAGATTTTGTCAC[A/C]ACCAGGCCTGCCCTA	84708
rs550117377	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53630048	TTAATCATGTTGAAA[A/T]CATGAGTATTTTCCC	84708
rs550126236	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53470936	TAATTTATAGATTCA[A/G]TGCCATCCCCATCGA	84708
rs550146757	snp	A/G	0.00398564	0.0444627	intron-variant	LNX1	GRCh38.p7	4:53579273	TATGATGGGTACGGT[A/G]GAAATCTTACACTTT	84708
rs550154491	snp	A/G	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53558877	TCTGTCAGGGACTGG[A/G]CCACATCCCCTCTTC	84708
rs550157680	snp	A/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461895	CAATGCTTGAATATG[A/T]ATTAGCAAAAAGTTG	84708
rs550165832	snp	C/G	0.0126979	0.078662	intron-variant	LNX1	GRCh38.p7	4:53562468	AGAGCTCTCTAGTCT[C/G]AAGACAATCAATGAT	84708
rs550176412	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53467959	CAATCTAGCAAGGCA[A/G]GCCAACATTCAAATT	84708
rs550189651	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53552716	TGCCTGTAGTCCCAG[C/G]TACTCGGGAGGCTGA	84708
rs550201020	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53596780	TCCAGCATCCCTGAC[C/T]TCCCCCTATTATAAT	84708
rs550214550	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53613791	TATGTGTCTTTATAA[C/T]AGAATGATTTATATT	84708
rs550218387	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53645841	ATATCTGAAACCGTA[A/T]GAAATACCAGACTCC	84708
rs550218794	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53465915	TAAAATGCTACTTTA[A/T]TATAGGAAGTCCACA	84708
rs550222739	snp	A/G	0.0107246	0.0724382	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53512376	TTCTAATCTCTGGTA[A/G]TTAAAAAAAACTGCC	84708
rs550234260	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53532540	TTTGCTTTCCATAAA[A/G]ACCCTGCAAAAGGCC	84708
rs550234381	snp	G/T	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519530	TAGGCCCATCTTATA[G/T]ATGGGGAAAATGAGG	84708
rs550242422	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53606650	CTGGCAGACATACAA[A/T]AAAAAAAGAAAACTT	84708
rs550248853	snp	C/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53599617	TCCAAGAACCCTCTC[C/T]TGGGGTCTGGATCGG	84708
rs550293999	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53549975	TTTTGTTTAGGGTGG[C/G]CTCCCTAGGAGGAGA	84708
rs550295564	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53518836	GAAAAGCATGGAAAA[C/T]TAGAAGCAGGTTTTT	84708
rs550302352	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53540066	ATAAAATAAGATGGC[A/G]TAGCAACTACCCCAT	84708
rs550339838	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53487438	ATAAACTATATAAAA[G/T]GCACTGGGTTCATTT	84708
rs550341045	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53509103	TGAACACTGCCACTC[A/G]GCAAGTCATTGCAGC	84708
rs550383522	snp	C/T	0.00119737	0.0244387	nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53603789	ACCAGGCCCCAACTC[C/T]GACACTGGAGATTAC	84708
rs550394034	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53631783	ATTCTCAAACCTGGC[A/T]GCAAACAGTCACCCC	84708
rs550398501	snp	C/T	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53587212	TGTCCTCATGTCACA[C/T]AGAACAAAATGGAGG	84708
rs550415550	snp	C/T			intron-variant, utr-variant-3-prime	LNX1, LOC101928879	GRCh38.p7	4:53577292	CTAGGTCTTTTAAAG[C/T]TTCTCTGTAGTGTTC	84708
rs550420571	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53610785	AAGAATAAAGAGAGA[C/T]AAATAAAGGCAAAAG	84708
rs550462119	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53504998	AAATGTGACACAGAG[A/G]CATGAAGTGAGCACA	84708
rs550471232	snp	A/C/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	LNX1, FIP1L1	GRCh38.p7	4:53462734	ACTCTAACCAGTTCT[A/C/G]AATCTATCGTCATAC	84708
rs550471444	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53531508	TGAGACACACGGAAA[C/T]AGACAGTAGTTGGGA	84708
rs550509459	snp	A/G	0.000399281	0.0141238	nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53604452	ATAAAAAGCAGAACT[A/G]GCAGAGCCTATGCCA	84708
rs550513815	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53542360	GGTAGGGGGTGGATT[A/G]AGCTGAATGCGCAGT	84708
rs550539849	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53641005	AAAGGTATTGGAAGG[C/T]TGGCTGCTAATTGGA	84708
rs550577544	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53549286	CTCAATGTTTTGGAC[C/T]TTTGCTTTCTTACAT	84708
rs550604094	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53541123	GCCTGGGTGACAGAG[C/T]GAGACTCTAACTCAA	84708
rs550620010	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53516069	CCGTAGCAGGACCCA[C/T]ATTCTACAAAAAAAT	84708
rs550630956	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53465754	ATGAAAAATATGTTG[C/G]TAGCTTTTTTTGAAG	84708
rs550645992	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53611299	AAAATGCACAACAAA[A/G]TTATACTAAAATATG	84708
rs550680002	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53472184	GAGTTCATGTCCTTT[C/G]TAGGGACATGGATGA	84708
rs550695506	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53515646	TGTAATAAAACTGAA[C/G]GGTAATGACCATAAC	84708
rs550695692	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53521707	ACGAAGGGGGAAAGG[A/T]GGGGATGCTTTTCCT	84708
rs550705647	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53636953	GTTCCCTCCCTCCCT[C/T]CCCAAGAAAGCAAAA	84708
rs550750618	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53499591	CTGAATTAATAGAAG[A/T]GAATGAATCATTTTT	84708
rs550779117	in-del	-/G	0.00795532	0.062565	intron-variant	LNX1	GRCh38.p7	4:53580548	GGAGTGGGTAGAGGA[-/G]GAGACACTGCCCTGA	84708
rs550802200	snp	C/T	0	0	intron-variant	LNX1	GRCh38.p7	4:53568748	CAGATGACATGATTG[C/T]ATATCTAGAAAACCC	84708
rs550806037	snp	C/T	0.0023933	0.0345097	intron-variant, downstream-variant-500B, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53459987	GGTTCCTGGTGAAAC[C/T]AAATGGGGTACACTT	84708
rs550807546	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53543851	AAACAAATCTCCATG[A/G]TGCTTTCTTTAGATG	84708
rs550808119	snp	A/G	4.99397e-05	0.00499673	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507482	GTGCTGAGGAATAGC[A/G]ACAGGAGGAACAGTA	84708
rs550830037	snp	C/G			intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53558701	TCCAAACAATGTACA[C/G]GTTCCTGTTTGGTGA	84708
rs550848120	snp	A/G	0.00279162	0.0372561	intron-variant	LNX1	GRCh38.p7	4:53467772	TGAATGAAATGAAGC[A/G]AGAAGAGAAGTTTAG	84708
rs550882970	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53550442	GACAAATCCAGGGAT[C/T]AGCAACACTTTTTTT	84708
rs550889114	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53641541	GTTTCTCCCCACCCC[A/G]CAATACCCAGGGGTT	84708
rs550954021	in-del	-/T			intron-variant, utr-variant-3-prime	LNX1, LOC101928879	GRCh38.p7	4:53577020	AATTGTAGCATTTTA[-/T]TTTAGCATCAGATAG	84708
rs550970471	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53493285	AAATGCCTCTTCTAA[C/G]TCTGGTTTTGTTCCC	84708
rs550974062	snp	A/C	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53471655	TACAAGAAAAAAAAA[A/C]CCCATCAAAAAGTGG	84708
rs551001879	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53582482	AAGAGTTCTCTCCAG[C/T]AAGGACACCACATGG	84708
rs551005790	snp	A/G	3.31225e-05	0.00406941	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508096	TCGTCTGTCATTAAG[A/G]AGATGGTGGCAGCTG	84708
rs551030803	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53535755	TTCCCTGCCTTTATG[C/T]CATCTCTCTTTCACT	84708
rs551033739	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53492857	TGAGATGCCTTTGCC[C/T]TATCCACAGGAAGAT	84708
rs551035450	snp	C/G	0.00716266	0.059414	intron-variant	LNX1	GRCh38.p7	4:53471293	GGCTAGCCATACGTA[C/G]AGAGCTGAAACTGGA	84708
rs551073209	snp	A/T	0.00478085	0.0486577	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53602731	ATGAAAAACACGTGT[A/T]GGGTGATAGTTCACA	84708
rs551080783	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53595984	ACAAAAACCTCTTTG[A/G]CTATCTTCTAAAGGT	84708
rs551083074	snp	C/T	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53555246	GGCCCAGCAGCCCTA[C/T]TTACTGTTCCAAATG	84708
rs551089747	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53467630	ACTACAATAGCCAAT[G/T]CAGAGAAGTCCTTAA	84708
rs551096169	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53561410	TTTTTCTATTTTTAG[G/T]AGAGATGGGGTTTCA	84708
rs551117939	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53529457	CTGCTTTACATTCAC[A/G]TATTTCTACATTCAC	84708
rs551139762	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53494320	TGTGAGGCCTCCCGA[A/G]CCATGTGGAACTGTG	84708
rs551141335	snp	G/T	0.00358779	0.0422022	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53502313	ACCTCTGAGATATTG[G/T]GGGTTTGGTTCCAGA	84708
rs551146798	snp	C/T	1.69836e-05	0.00291402	intron-variant	LNX1	GRCh38.p7	4:53478794	CACAACTCTGGTAGT[C/T]TTTGAATGTAGAAAA	84708
rs551150285	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53617196	TAAGACCTAGTACCT[A/G]GTCTAATAATAATAA	84708
rs551157054	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53484846	TAGAAAATCCTTCTG[A/C]AAAGGGCCCAAAAAA	84708
rs551159537	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53568633	CTCTCACCACTCCTA[A/T]TCAACATAGTGTTGG	84708
rs551184157	in-del	-/AGTT	0.00304955	0.0389291	intron-variant, downstream-variant-500B, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460228	CATGAGTTTTTATAC[-/AGTT]AGTTACTAACGATTG	84708
rs551187901	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53610061	TTAACCTCTGTGTCA[C/T]GCTGCTTCCCAACAC	84708
rs551202264	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53614351	ATGACACACCATTTC[A/C]TCTCACAAACAGCAC	84708
rs551214184	snp	A/G			missense	LNX1	GRCh38.p7	4:53496304	GGAACTTCTGTTCAC[A/G]CATCACAGTCAGCCA	84708
rs551214356	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53470906	TTATCATGAAAATGG[A/G]CATACTGCCCAAGGT	84708
rs551222626	snp	A/G	0.00676609	0.0577691	intron-variant	LNX1	GRCh38.p7	4:53616478	TTTCTTAGTACTTGG[A/G]TTTGTCACAGAATGA	84708
rs551224623	in-del	-/T	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53632118	TACCAAGGGCAGACC[-/T]TAGGGCTGCATTATG	84708
rs551244446	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53596696	TCCACATACCAGATT[G/T]AAAATGTCTCTTCTC	84708
rs551246372	in-del	-/GAG	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53571499	GCTCTGAAGATGGAA[-/GAG]GAGGCCACGAGCCAA	84708
rs551249159	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53543120	CCTGCCTCAGCCTCC[C/T]GAAGTGTTATAATTA	84708
rs551263166	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53485677	ATATAAGGTGGAAAA[C/T]GGGCTAATATGCTTG	84708
rs551281308	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53596179	GTAATAATCACAAAC[A/T]TCAGCTGATGTGATA	84708
rs551289683	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53616513	TCTGATTCATTTGGC[C/T]TACCTGGGCAGCTTT	84708
rs551333160	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53589878	GTCTACAGCTTTGTT[C/T]CTTTAGTACTCAGAC	84708
rs551341601	snp	C/T	0.00279162	0.0372561	intron-variant	LNX1	GRCh38.p7	4:53643457	CCCGGTCAAGAAACC[C/T]TGGTCTTTATGATCT	84708
rs551354981	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53611805	TACCAAGAAATCTAG[C/T]GGATTATATGTACTG	84708
rs551379229	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53488311	GTTATGCCCAGTAGG[A/G]CAACCCCACATCAAT	84708
rs551381186	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53547880	GATGAATATGGTTCG[C/G]GGGTCCTGGCATGCA	84708
rs551385713	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53649546	AGCCTGCACCTGTCT[A/G]GACAGCTCCTCCTCT	84708
rs551392147	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53555491	ACTCTACTTATAAAT[G/T]ACTTATTTCCATCTG	84708
rs551392554	in-del	-/T			intron-variant	LNX1	GRCh38.p7	4:53532066	TATTCAGTCTTGCAA[-/T]GAGAAACAAGGATGA	84708
rs551418034	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53648023	TGGACACTTGGGTTG[A/C]ATGTACCTTTGGGCT	84708
rs551424822	snp	A/C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53648977	TAGAAGAGAGGAGGT[A/C/T]TCCTTAGCATGCAGG	84708
rs551459605	snp	C/G	0.000798403	0.0199641	upstream-variant-2KB	LNX1	GRCh38.p7	4:53654025	TTTGGCGACGCTTTG[C/G]GGGTATTTTGCCCTA	84708
rs551492226	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53554043	GCCTGTCCCAGGAAA[C/T]GTGGGCTGTATAGGA	84708
rs551497625	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53521266	AAGTCTATGCAACCC[C/T]AGGGGCTCTGCAGAG	84708
rs551498583	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53642135	GCTAAGATGGGAGGA[C/T]TGCTTGAGCTCAAAA	84708
rs551552054	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1, LOC101928879	GRCh38.p7	4:53575471	TGATATGCAGACCTT[A/T]GAGAGAGACTTAAAG	84708
rs551552649	in-del	-/A	0.00557542	0.0525036	intron-variant	LNX1	GRCh38.p7	4:53630176	CAGGAGCTCCTGCTT[-/A]AAAACAGGGACTTTC	84708
rs551588899	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53582449	CATGAGTACATAAGC[A/G]AGCCCAGTCAAGTAA	84708
rs551617547	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53466550	AAGGCGTCGCCTCAC[C/T]CGGGAAGCACAAGGG	84708
rs551622378	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53480899	TAAGAATTTTTTTTA[C/G]TTACAAGTGATGCCA	84708
rs551644731	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53550877	AAAGCCAGACCAGGG[C/T]GTAATGGATAGATGG	84708
rs551653878	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53535951	ATACCAAAGGATTGG[A/G]CTTAGTCAAGGTCAG	84708
rs551659225	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53506735	GTTGTGGGTGCCTGT[A/G]ATCCCACCTACTTGG	84708
rs551690186	snp	A/G	0.00398564	0.0444627	intron-variant	LNX1	GRCh38.p7	4:53467920	GGAAAACACTCTGCA[A/G]GATAATATCCAGGAG	84708
rs551715211	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53540782	ATTTAAGTATCCTCA[A/C]TTATTGGGGTCAAAC	84708
rs551716719	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53545224	AATGGGAAAATAGTT[A/C]TACAAACTAGGAACT	84708
rs551732819	snp	G/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53549466	GAGGAGGAGGAGGTT[G/T]AAAGAAACTTAAGAG	84708
rs551742055	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime, downstream-variant-500B	LNX1, FIP1L1	GRCh38.p7	4:53459903	GTGACACTCTTGCTT[A/G]GTATATTAAGAGACT	84708
rs551746608	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53492781	GAATGGCCTAGGGGA[A/G]AGCACGTTGGGCAAG	84708
rs551768663	snp	A/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53635668	GATTCTATGCAACTC[A/T]TGAAAAACAAGCCAT	84708
rs551778115	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53544647	CTGCCCAGTACCATG[C/T]GAGAATCTTTTCTAA	84708
rs551791511	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53588609	AGTCTGACCTACCCA[C/T]CTGGACATGCAGCCC	84708
rs551800938	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53528260	TTATCCATAGTTTTG[C/T]TTTCCGCAGTTTCAG	84708
rs551807360	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53641734	GCTTTCTATAACTAG[A/G]CTGCTTGCACATTCC	84708
rs551809147	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53645084	GCCAGGCAGTGTCCA[C/T]GCCAAAAAAGAACAG	84708
rs551812774	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53496974	GATACTGTGTGTGTG[C/T]GGATGGGAATGTGTC	84708
rs551813076	in-del	-/A			intron-variant	LNX1	GRCh38.p7	4:53526621	AATGCCTTTCCATGT[-/A]AATCTAGTATCTGCT	84708
rs551848673	snp	A/C	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53537954	CAGAATATCCTAAGG[A/C]TGGGGGAGAGAGCCT	84708
rs551898224	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53524607	TCTGTAATGCTTTAA[A/G]CCTACGCTCTTTCTA	84708
rs551903427	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53632398	ATGGCTGCCTCCCTT[A/C]TCAGACACCTGCCTT	84708
rs551907488	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53472620	GAAAAAGGTACAAAT[C/T]TTGATTTTCTGTATT	84708
rs551911724	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53464613	TCTATATGCATACTT[C/T]GAACAAACAGGTATA	84708
rs551920420	snp	A/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53535713	CTATAGCCAGCGCCT[A/T]ACATATGCCATGTAC	84708
rs551932601	snp	A/T	0.0138799	0.0821421	intron-variant	LNX1	GRCh38.p7	4:53567941	CTCTCCCAAGACTAA[A/T]CCAGGAAGAAGTTGA	84708
rs551936730	snp	C/T	0.00993419	0.0697739	intron-variant	LNX1	GRCh38.p7	4:53485514	GGCTTTGGTATTAAG[C/T]TGTTGACAGGAATAA	84708
rs551943460	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53474604	TTTACATTCTTTGGT[A/G]CATTCTGAATTTTCT	84708
rs552006945	in-del	-/TT	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53581432	CCAAAAACCTTCCTC[-/TT]TGCTCACTGTATTAG	84708
rs552007110	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53630079	ATGAAAATAGTTTCT[C/T]CATTAAAAAAAGGTG	84708
rs552013258	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53623127	TGATCACTTGAATAC[A/G]TTGCACGGCTGGACT	84708
rs552089242	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53490101	GTCAAATGTTCTTTG[A/T]TGAAATGAATTCTCA	84708
rs552098622	snp	A/T			intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53559647	TTAGCTTAATGTTAT[A/T]GTATTTTATTTTTTT	84708
rs552118533	snp	C/T	0.00279162	0.0372561	intron-variant	LNX1	GRCh38.p7	4:53564702	GAGCGACACAGAAGA[C/T]GGGTGATTTCTGCAT	84708
rs552131501	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53632915	CTCCTCCTGATTACA[C/T]TTCCTCAAGATATAT	84708
rs552142344	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53629395	TGGCAAAGAGGCAGA[C/G]TTGCAGTGCTAAGAG	84708
rs552157370	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53624755	TTGGTCCTGCAGGCC[A/G]TCTACCTCCTGGAGC	84708
rs552159092	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53586047	CTACCCTATTAGAAA[A/G]TGTATTAATTTCCCT	84708
rs552169047	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53545095	TGCAATAAGATCCCT[C/T]TGATCCTTTGTAATC	84708
rs552235356	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53582904	CCAAACAGACCAGCG[C/T]CTGCCACTTCTTCAA	84708
rs552246118	snp	A/T	0.00478085	0.0486577	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53504119	CAACCTGGGCTACAG[A/T]GCGAGCGAGACTCCG	84708
rs552246253	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53495862	TAATGTTCTTACCTG[A/G]GCAGAAGCTTTGAAA	84708
rs552248182	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53592063	GCAGTTTCAAAGTGG[G/T]TTTCAAACACTTTTG	84708
rs552259410	in-del	-/A	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53482429	CTTTACCTTCAATTC[-/A]CAATCACAAAGACAT	84708
rs552261060	snp	A/G	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53618058	ATAGTTTTTATAATC[A/G]AAAGATACTGTGATT	84708
rs552262151	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53463579	AGGTGGCTTTAAACT[G/T]TGAATGTGAATGTTG	84708
rs552266236	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53510569	TCATTCTGTTTAAAC[A/G]TAGTGAAGAGGTTGA	84708
rs552288576	snp	C/T	0.00318978	0.0398085	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53599002	AACAGAGGAGTGTTA[C/T]AGATGCAGTTACATG	84708
rs552325674	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53598448	TAGTTGCCCAGGCTG[C/G]TCTCGAACTCCTGGG	84708
rs552376417	in-del	-/A	0.00636936	0.0560724	intron-variant	LNX1	GRCh38.p7	4:53606359	GATCCCTGGAAACAT[-/A]ACAACCTCCCAAGAT	84708
rs552382443	in-del	-/A	0.00279162	0.0372561	intron-variant	LNX1	GRCh38.p7	4:53538852	GGGGAGAAAAAAAAT[-/A]AAAGGTAACTGAAGA	84708
rs552411877	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53489297	AGGGCAGCAATATGG[C/T]TTATTTTTCCCAGTA	84708
rs552413019	snp	A/G	0	0	intron-variant	LNX1	GRCh38.p7	4:53650137	TGATGCTGAGGACAC[A/G]TGCCCTGCCTGTATG	84708
rs552413233	in-del	-/AAGA	0.0197687	0.0974348	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53601075	AGAGGAAGATTCTGC[-/AAGA]AAGAAAGAAAGAAAG	84708
rs552440807	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53536459	CTAGATCACCAGCAA[A/C]TCCTGACCTAAAAAA	84708
rs552452641	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53585270	GTACAAAACACTTAC[C/T]ACTGTGGCATGAACA	84708
rs552460630	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53522290	AGGCCTGCCTCTCAT[C/T]TCACTTTCTCCACTG	84708
rs552486973	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53618943	TTTTTGTAGATACAG[A/G]GTCTTGCTATGTTAC	84708
rs552500819	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53556892	TCTGATCTGAACTCT[A/G]TGAACTCTATTTAAA	84708
rs552532547	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53479875	ACAGAATGACCTACC[C/T]ATGTACCTCAAAACC	84708
rs552545083	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53487270	AGGGCCAGTGAAAAC[A/G]TACAGGGGGAGTAAG	84708
rs552546950	snp	A/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53598158	TTATAGGACCTTCCT[A/G]ACTTCCCTAAGCAGA	84708
rs552568130	snp	C/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53480693	GGAGAACCTGGAGGG[C/G]TGTATAACCTTGTAG	84708
rs552584713	snp	G/T	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53516171	TGCTTGAGCCCAGAA[G/T]TTCAAGCCTGCAGTA	84708
rs552585731	snp	A/G	0.00755907	0.0610114	intron-variant	LNX1	GRCh38.p7	4:53570571	CTAATGCTAAATGAC[A/G]AGTTAGTGGGTGCAG	84708
rs552588967	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53475908	GCCCTAAGGAGAGAT[C/G]ATCTAAGAAATGTCT	84708
rs552615912	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53610600	GTAGTCCCAGCTGCT[C/T]GCGAGGCTGAGGCAG	84708
rs552627807	snp	A/G	0.00318978	0.0398085	intron-variant	LNX1	GRCh38.p7	4:53537030	CTGCTTTTTTATAAC[A/G]TGAGCCACTAGGCAT	84708
rs552629145	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53651017	TATTACCATCATTCT[C/G]ATTTTACATATTGGC	84708
rs552635635	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	LNX1, LOC101928879	GRCh38.p7	4:53576716	AAGTAAATTAAAAGA[C/T]CTTATGCTTTCCACA	84708
rs552648423	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53590204	ATTCTTAGTGGTGAG[A/G]AACGACTGTCTGTCT	84708
rs552663948	snp	A/G	0.00159617	0.0282053	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53601523	GGACCAACACTGTTC[A/G]CGTTCTGGCCACCTG	84708
rs552724592	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53611630	GTTGGGGCAAAAGTA[A/C]TTGTGGTTTTTACCA	84708
rs552725484	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53564315	CCTCACAGAGTTCCA[A/G]CAGCCACCTGCTAGC	84708
rs552732551	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53557404	AAAATAACATGGATA[C/T]ATACATTTTATACAT	84708
rs552745113	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53563249	TATTTAGATGCATAT[G/T]TATTGAGTAAAGTGA	84708
rs552797761	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53480299	TTCCAGGAATTAAGA[C/T]ATATGACAGAGGGTT	84708
rs552800839	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53501064	CAACACCAATGAGAT[C/T]CTAGTGACCTTAAAG	84708
rs552808149	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53479353	TATTTTATAGAGTCT[G/T]CTTTCACACCTGCTC	84708
rs552810816	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53589492	CAACCTAGGAAAATT[A/C]CTTCCAAAGGAAGAA	84708
rs552817441	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53468362	AAATATGGAAAGGAA[C/T]AACCGTTACCAGCTA	84708
rs552865142	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53474659	GGAGAGGATGGAATG[A/C]AAGAAACCAGGAATC	84708
rs552873792	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53542217	ATTAGGAAAGTAAAA[C/T]TGAGTTTCCAGAAAA	84708
rs552899239	snp	C/G	0.000399281	0.0141238	nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53604700	TTATGAATATCAGTC[C/G]AAAGTCAGAGACAGA	84708
rs552949910	snp	G/T	0.0912534	0.193131	intron-variant	LNX1	GRCh38.p7	4:53570124	TTCCTCAGGGATCTA[G/T]AACTAGAAATACCAT	84708
rs552953925	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53487906	TTTTTCAACATATGC[C/T]TGTGGGGATGGCTCT	84708
rs552965501	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53494557	CAGGCCTAGTCAAGC[A/C]AAAATCTCCCCTGCG	84708
rs552988167	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	LNX1	GRCh38.p7	4:53653541	CCGCTGGCTGCGGTG[C/G]CTTCAGCTCTCCACT	84708
rs553010509	snp	A/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53590005	TGAGGAGAGGTTTAG[A/T]TGCACTTTTATCAGA	84708
rs553033294	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53641526	AACGACCATGCCTCT[C/G]TTTCTCCCCACCCCA	84708
rs553041504	in-del	-/GGCAAAGTATGATTCCC	0.00676609	0.0577691	intron-variant	LNX1	GRCh38.p7	4:53555785	GTAATGGTGATTCCT[-/GGCAAAGTATGATTCCC]GGCAAAGTATGATTC	84708
rs553049159	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53596894	CATTTCAAAAGAAAT[C/T]TGAGAATGCAACTCT	84708
rs553054747	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53637854	TGCTGACGGAGATTA[C/G]ACCACCACTCAAAGT	84708
rs553060591	snp	A/G	0.00398564	0.0444627	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53521010	ACTTTTAAAACACTT[A/G]GAGACAACCAAAGTC	84708
rs553067744	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53550076	ATTCTCAAAGGGGGG[A/G]AAAAATAAAATCATG	84708
rs553073123	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53511150	ACTCACGTGCTTTGT[A/G]TAATAAAGGTTCTGC	84708
rs553075740	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53562966	CCGTAATCCCAGAAC[G/T]TTGGGAGGCCGAGAC	84708
rs553076971	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53471386	CTAAAACCATAAAAA[C/T]CCTAGAAGAAAACCT	84708
rs553096590	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53638032	CCACGATGGTGGCAT[A/T]TTAACAAGAAACAAC	84708
rs553096733	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53535423	CCATCAAGAATAGCA[A/C]ACTTTATTTCACTCT	84708
rs553103369	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53616056	CTCACCACCCCCGTC[A/C]TTCCAAGACTCTTGT	84708
rs553110041	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53509120	CAAGTCATTGCAGCG[C/T]ACAGGCTAGGTTTTG	84708
rs553139854	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53568169	GCTTCATTCTGATAC[C/T]AAAGCCGGGCAGAGA	84708
rs553149957	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53556198	TTGAAGAGGACACTG[A/G]GGAGAAGGACATGTA	84708
rs553158339	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53575271	ACAGGTGTGAGCCCC[C/T]ATGCCCAGCCTAGAT	84708
rs553162017	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53555681	ATCCCCAGTAGCATC[A/G]GGGAACAGCTGCACA	84708
rs553167251	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53462448	TTTGTAGCTGTAGTC[C/T]GGGAATTGGTTTGAA	84708
rs553240388	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53623425	TTTTTGGTAGAGACA[A/G]GATTTCACCATGTTG	84708
rs553257956	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	LNX1	GRCh38.p7	4:53654204	AAGTGCAGTTTTTAG[A/G]TATGTTTATGGACTC	84708
rs553265667	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53584664	ATGTGACCCATATGA[C/T]GACCTCTATGTGAGG	84708
rs553268068	in-del	-/T	0.00318978	0.0398085	utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460523	ATGCATTTTAAAAAA[-/T]ATTTTAGCTGTAAAT	84708
rs553317711	snp	C/T	0	0	intron-variant	LNX1	GRCh38.p7	4:53642912	TGTAACTTTAGTCTC[C/T]TTTTGCCTTTGGGTG	84708
rs553331442	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53623937	CTTTTAGCTTGAATA[A/C]AAACTTGCATCAAAA	84708
rs553333861	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53558332	AGCAGACAGGCTGGG[A/C]GTTAAAATGTGTTGG	84708
rs553377039	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53609395	AACAATATGTTTTAA[C/G]CCATAAACCATTGCC	84708
rs553471654	snp	C/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53564792	GTGGGTGCGCGCACC[C/G]TGCGCCAGCCGAAGC	84708
rs553497151	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53532347	CGGGCGTGTTGGCAC[A/G]CACTGTAGCCCCGGC	84708
rs553506377	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53606082	AGTTAGCAGAAGACA[A/G]GAAATAATCAAAATC	84708
rs553522785	snp	C/T	0.00358779	0.0422022	intron-variant	LNX1	GRCh38.p7	4:53548426	ATATGTATATAATTT[C/T]ATATAGATAACTATA	84708
rs553541502	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53467717	CTCAGTAGCCGATGC[A/G]ATCAACTGGAAGAAA	84708
rs553541763	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53639797	AGCACTTTGGGAGGC[C/T]GAGGCGGGTGGATCA	84708
rs553550098	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53466509	GACAGTGGGTGCAGC[A/G]CACCGAGCACGAGCC	84708
rs553555259	snp	C/G	0.000399281	0.0141238	nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53603838	GGTGGGGACAAATAT[C/G]CAGACTATATCGGGG	84708
rs553561932	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53649723	TTGGGCATCTCCTCT[A/G]TGCCCACCCAGTCTG	84708
rs553580978	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53646760	CTCCAGTTGGAGCAA[C/T]CACAGTTTCTTTGTA	84708
rs553593865	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53637413	ATGATGTTCCTTAGT[A/C]ATGTCAAAAGTAAAA	84708
rs553601193	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53471777	AAATGCAAATCAAAA[A/C]CACAATGAGATACCA	84708
rs553606867	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53489626	AAGTTTCAAGATCCC[C/T]TAATATTTGCAGTGT	84708
rs553612162	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53612909	AAAAAGAAGAAATTA[A/G]TTGTGCTAGTTGACA	84708
rs553638653	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53648804	CCTGCCCTTCCATCC[C/G]CCTGAACACATTCAT	84708
rs553678958	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53641192	GCCACTTTCTCTGTT[C/G]TGGGGAAGGGCGGGG	84708
rs553694616	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53518160	GGCTTGTCAGGGTGC[A/G]GCCAGGAGAGGCGTG	84708
rs553699285	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53545960	GTACAGTGCACCTCA[C/T]CATGCCCAGATAATT	84708
rs553709130	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53514574	GTATGGGGGAACTGC[C/T]CCCATGATTCATGGA	84708
rs553722288	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53465632	CTTCCTTAGTTTTGT[A/G]TGGTCCAGAGCTAGT	84708
rs553739560	snp	G/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53613088	AGGAAAGACACATAC[G/T]AGATTATTAATATGG	84708
rs553740933	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53633338	GGTCCCCCATGCACA[A/G]TAACTTTCTTAGTCT	84708
rs553756853	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53470020	TCCTGATAACAAAGC[C/T]GGGCAGAGACACAAC	84708
rs553776768	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53606300	TCAGAAATTATTATG[A/G]ACACCTCTATGCACA	84708
rs553779855	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53510753	AGCTGGTCTGGAAAT[A/G]GTCTTTTCTGAGGAG	84708
rs553798768	snp	C/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53572244	TTTCAGCAAAAGTCA[C/G]AAATAGACTACCCTA	84708
rs553834287	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53464078	CAGAGGTTGGAAAGA[C/T]GACAGTGGATGTAGG	84708
rs553847275	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53605638	CTGTTTCTCTGTATT[C/T]ATGTTTTTTTTAAAA	84708
rs553852343	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53474827	GCTGGAGTGCAGTGG[C/T]GCGATCTCAGCTCAC	84708
rs553878676	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53620062	GTAACGAAACACATT[A/G]TGGCTTTTGTTAAAC	84708
rs553885900	snp	A/C	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53612269	TAAGGGAGAACTTTC[A/C]TACAGCTTAGGTAGA	84708
rs553888415	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53593186	TTGATAATTGAGAAA[C/T]ATCACTCACACAAAG	84708
rs553908333	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53531345	CTCACTTCATTCTCT[C/T]AAGTAAATCACTTTA	84708
rs553914289	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53532686	AGTTCCAACCACAGG[A/G]GACAGACTAAACAGA	84708
rs553928837	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53546572	AGCTTGTTACTGGCA[A/G]GGCTGAGTCATTTGG	84708
rs553945922	snp	C/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53563452	AATATCCCTCCTAAG[C/G]GGAGTAAGAGGGGGG	84708
rs553961717	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53625737	GCTTGAGCATGAGAG[G/T]TTGAGGCTGTAGTAA	84708
rs553968348	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53517024	TCTCCCAGCAGAATA[C/T]AGATAGCTTCCATGG	84708
rs553970827	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53600810	ATCTTGGCTCACTGC[A/G]ACCTCCAGCTCCTGG	84708
rs553972521	snp	A/T	0.00199481	0.0315187	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53598068	CATGCCTGGTTGGTT[A/T]TGGGCAGACTTGAGA	84708
rs553990710	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53590318	AGCATAATTCCTAAC[A/T]GATTATTCCCTTGCA	84708
rs553999485	snp	A/T	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53625764	GTAAGCCACGACTGC[A/T]TCACTGCACTCCAGC	84708
rs554000613	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53645923	TCACTCAGAGTTTTC[C/T]TATAAAGCTGATATA	84708
rs554019654	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507208	AATATTGTATACCCT[C/T]GGGAAGAGAGGGGTC	84708
rs554029783	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53538674	TCACTTGATTCATCT[A/C]TTATTCAAAAGCTGT	84708
rs554038255	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53505459	GTTTCACTGTGTTGG[C/T]CAGGCTGGTCTCAAA	84708
rs554074483	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53647982	ATCCCATTGTATGTG[C/T]ATACTACATTTTGTT	84708
rs554085746	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53553004	TTCCCTTCCGTAGAA[A/G]CCAACCAGGGTCTTC	84708
rs554107217	snp	C/G	0.000798403	0.0199641	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53600197	TGTTTTTTATGCTGT[C/G]CAATAGAGTACTCTG	84708
rs554122212	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53639901	AGCCAGGCATGTTGG[C/T]GCATGCCTATAATCC	84708
rs554130777	snp	A/G	0.00636936	0.0560724	intron-variant	LNX1	GRCh38.p7	4:53563566	TTGAGACAGAGTCTC[A/G]CTCTGTCACCCAGGC	84708
rs554144438	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53606915	TTCAACATCCCTTCA[C/T]GTTAAAAACCCTCAA	84708
rs554148748	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53592307	GTCAGAGTTATTTCT[C/G]TCCCAAGCGTGGTGT	84708
rs554178244	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53463330	CTGAAGCATCCATTC[A/G]AGTTGATATCAGTGT	84708
rs554213028	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53468482	GACAGGATCAAATTC[A/G]CACATAACAATATTC	84708
rs554215815	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53557585	TACGGAAGGAAGAGA[A/G]GTTACATCTATTGAG	84708
rs554222275	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53532254	GCTGAGGCAGGCAGA[A/T]CACCTGAGGTCAGGA	84708
rs554245805	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53516507	TCTGCTTGGGGTAAT[C/T]GGAGAAGGCTTCTTA	84708
rs554277118	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53557133	AAAATATCACTAGAG[A/G]TTGGTGACATGAGGC	84708
rs554279390	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53626262	ATAGAAAAAGATCAC[A/G]AATTGGTCCAGAGTT	84708
rs554300319	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53465034	TTGATAATTGTTATC[A/C]AGTTACATCCTAACA	84708
rs554309537	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53650230	GCGCGTGTCACAGTC[C/T]TTAAATACATTACAT	84708
rs554368535	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53538196	CATGGCTTGAAGGAT[A/G]GGCATGTGGATTGCT	84708
rs554378910	snp	C/G			intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53559221	AGAGGCAGGGCTAAA[C/G]AGTTTAAATACAGAA	84708
rs554383514	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53481305	CGGCAAACACAAACA[A/G]AAACTAAAAGTAGCG	84708
rs554384942	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53488765	CCTGAGACCACATGA[C/T]GCCATACAGACCTTA	84708
rs554418984	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53564222	GGGGTCACACGGGCT[G/T]CATGGGCTAAGGGTG	84708
rs554422812	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53606791	TCCCTGGGATGCAAG[G/T]TTGCTTCAACATACA	84708
rs554444428	snp	A/T	0.00636936	0.0560724	intron-variant	LNX1	GRCh38.p7	4:53617472	GAAACCCAAAGCTGT[A/T]AACACAGCTGGGGAA	84708
rs554448679	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53585371	TCAGCCTCCAAGTGG[A/G]CAAGAAATCTCTCCA	84708
rs554450908	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53578311	GCGATTTGGTCCTTG[A/G]GTGAACATCATAGAG	84708
rs554460016	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53600291	TAACATAAAGTGACT[C/T]GAGGACACATGCACA	84708
rs554465444	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53645879	GCATTGGTGAGGATA[C/T]TGATTACTATTTCAT	84708
rs554470490	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53591579	ACATCACGGAAGCCC[C/T]GACAGATAAAGCATT	84708
rs554486849	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53544895	AGCCAGCAATTGGCA[A/G]GGCCAGGCTCTAACT	84708
rs554537203	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53474710	TGTTGTCTATGCCGG[A/G]ATATCATGCTTCCTT	84708
rs554541832	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53644358	AGTGAGCCGAGATCA[C/T]GCCACTGCACTCCAG	84708
rs554564915	snp	C/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53531223	GTCTAGCAGGAAGTG[C/G]TGTGGACATGAGGTG	84708
rs554571197	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53612500	TAATGGAGGATAGCT[A/G]AATAAATTATGGCAT	84708
rs554575223	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53571562	GGCAAGGAAAGGGAT[G/T]CTCCCCTGAAGCCAA	84708
rs554578533	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53505559	GTCTGGCCCAAGTAG[C/T]AGAGAACTTTACATG	84708
rs554606378	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53619457	ATGCAATATGTGGCC[A/T]TTGTGTCAGACTTCT	84708
rs554608580	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53524859	GGAAGGAACCCTTTC[A/T]TTGCAAAAAAAGCTC	84708
rs554638972	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53509238	GAAATCATATCACGA[A/G]CCCCTTTAGGAAGTG	84708
rs554641961	snp	A/G	0.00597247	0.0543191	intron-variant	LNX1	GRCh38.p7	4:53537056	GGCATGCCATTAGGT[A/G]AAAAGACTCACCTCT	84708
rs554651664	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53481200	TGGATTTGAATGCCA[C/T]ATAACATGTGCTCTC	84708
rs554671484	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53473181	ATGAACAAGAGCTCA[A/G]TGCAGAGATAAGACT	84708
rs554672713	snp	A/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53611020	TGATGGTAGCAAATT[A/T]TAAAACTGGAATAAA	84708
rs554729291	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53585940	GGGTGAATGCTCCCA[A/G]CGATCCTTTCCAACA	84708
rs554735725	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53544759	CAATAATGCCCATGC[A/G]CCAGGCACTGTACTG	84708
rs554737145	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53649876	GGTTTTAAATCTCTA[C/T]GTTCCACCCTAGCCA	84708
rs554743279	snp	C/T	0.00159617	0.0282053	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53522327	CATAGTGATCTCTCC[C/T]CTCTCAATGCATTTA	84708
rs554748472	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53552306	TCAAAGCTCACTCAG[A/G]CTTTGTACCACAGGC	84708
rs554777222	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53645438	ATTGGGGTTACCCAA[A/T]GGGGTCTATTCCAGA	84708
rs554818308	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53468956	AGTTAACAAGGATAT[C/T]CAGGAATTGAACTCA	84708
rs554866758	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53483684	GGAGTAAGGTTTGGT[G/T]GTTCCTCTCTTCATC	84708
rs554872972	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53620953	GGTTTAAAGAAATTC[A/T]ATTATAGTTGTTACT	84708
rs554905712	snp	C/T	0.000399281	0.0141238	nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53604786	GTGCTTGTGTTTGGA[C/T]TGGAGCTGAGCCTCT	84708
rs554911294	snp	A/T	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53506335	AGAGCTCAATTTTTT[A/T]AAAAAGCTGTTACTA	84708
rs554913262	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53513583	GTTACTAAATAGCTC[C/T]TTATCTGTCATTCAG	84708
rs554930509	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53612902	AAAAATAAAAAAGAA[A/G]AAATTAGTTGTGCTA	84708
rs554948935	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53517450	GTCCTATCCCTGCTA[A/G]TTGAGTCCTGATCAT	84708
rs554957572	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53636944	AGACCGCAGGTTCCC[G/T]CCCTCCCTCCCCAAG	84708
rs554987398	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53525315	GGTGAAACCTGGACT[C/T]TACTGAAAATACAGA	84708
rs554994059	snp	A/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53595476	TTCTTATGCATGACA[A/G]TGGTTTTCAGCATTG	84708
rs555014332	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53601772	CTACTTTCAACTCAT[C/G]TCAAGATGGCATCTT	84708
rs555027606	snp	A/C	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53512984	ATCTCCACGGCCAAA[A/C]CCTGGAGCTGGTCCT	84708
rs555031943	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53608709	AGACAAGGAAACAAC[C/T]TAAATGCCCATCAAC	84708
rs555050897	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53562073	TTTTTCTTTCATTCA[G/T]GGCCTGACCTATTGT	84708
rs555064889	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53510244	AGAGTCTAGTTCACC[A/G]ATCTATGCATCATGG	84708
rs555072984	snp	G/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53522623	CCACTGTACATACAG[G/T]GTTGAAGACACAACA	84708
rs555118624	snp	A/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53629717	ATTTTTAGGGTAATC[A/T]GAGGTGGTAGGGTGG	84708
rs555120509	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53483560	GAAGTAGCCAGCTGA[C/T]CTCATTTATCACTTT	84708
rs555140872	snp	C/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53545857	CTGTCGCCCAGGCTG[C/G]AGTACAATGGTGCTA	84708
rs555141582	snp	A/G/T	0.00239393	0.0345281	intron-variant	LNX1	GRCh38.p7	4:53470661	AGGATACAAATCAAC[A/G/T]TGCAAAAATCACAAG	84708
rs555155676	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53636531	ACCTTCAAGTATCAG[G/T]TCCTTGAACCATAAA	84708
rs555163690	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53541124	CCTGGGTGACAGAGC[A/G]AGACTCTAACTCAAA	84708
rs555182180	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53512750	TTAGGGGACTCTGTA[A/G]GGAAGTAAGTCTCCT	84708
rs555192360	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53635867	ATATGAGAGTACTTC[C/T]TGTCCTAACTGCAGC	84708
rs555207823	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53550786	GGCCCAGGTCTGACT[A/G]AAGTTAGTAGGCAGG	84708
rs555213382	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519787	TGGGCAGGATTATTA[C/T]CCCCAGTTTGCAAAT	84708
rs555241049	snp	C/G	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53591459	CCTTGTGGGTGAACC[C/G]AGCAGCTCCTTGGGC	84708
rs555272004	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53630677	AGTTTGATGTTAGTG[A/T]ACCAACAACATATAT	84708
rs555294891	in-del	-/A			intron-variant	LNX1	GRCh38.p7	4:53563461	CCTAAGGGGAGTAAG[-/A]GGGGGGCCTACTGGC	84708
rs555322339	snp	A/C	0.00119737	0.0244387	intron-variant, downstream-variant-500B	LNX1, FIP1L1	GRCh38.p7	4:53463000	ACATTCCCACCTGGG[A/C]GGATGTGTGCCCAAT	84708
rs555348733	snp	A/C	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53470987	CAGAATTGGAAAAAA[A/C]TACTTTAAAGTTCAT	84708
rs555392374	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53594803	TGCAGCCCCAACCTC[C/T]TGGGCTCAAGTGATC	84708
rs555410440	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53466383	AAGACAGCCGAATAG[G/T]AACAGCTCCAGTCTA	84708
rs555414169	snp	A/C	0.00914312	0.0669923	intron-variant	LNX1	GRCh38.p7	4:53566606	TAACGAGCAAAATAA[A/C]CAGCTAACATCATAA	84708
rs555417419	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53593026	GCTTAAAACAACAAC[A/C]ACCACCACAACAAAA	84708
rs555420196	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53520203	CCTCTCACAGCAACC[C/T]CTGCGGGTCCAAACC	84708
rs555430281	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53600977	CAGCTACTCAGGAGG[C/T]TGAAGCAGGAGAATC	84708
rs555444859	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53652101	GCTGGAGGCTGAGTG[A/G]GCAGAGGTGAAGTTT	84708
rs555459222	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53592453	GCATCTTCCCAGGAG[A/G]GCTGTAAACATCTCC	84708
rs555474007	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53559864	TGAGGGTCCCTCTAT[A/G]TTGCCCAGGCTGGTC	84708
rs555478939	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53586553	CCACATATTCTAAGT[C/T]ACAAATTAGTGATGT	84708
rs555479676	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53464277	AATGTACAGCCTCCT[A/G]CTTTGATTAACCTAG	84708
rs555480493	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53546501	CACATATCATAAAAC[A/G]ATGAATGCTTTACTC	84708
rs555490869	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53589608	CCACATTAGATCATG[A/G]GGATTATTATCTCCC	84708
rs555497376	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53541770	GTAGGCCAAGAAGCT[C/T]GAAGGAACACAGATT	84708
rs555503889	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53614252	TCCCTACATATTCTC[C/T]AGGAAAGAATTACTG	84708
rs555538849	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53557739	CGTTTTAAACTGCTG[A/G]CAGGGTGCTTTGTCC	84708
rs555543794	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53552787	TGAGCCAAGATGATG[C/T]CACTGTATTCCAGCC	84708
rs555552295	snp	G/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53629018	TTCAAAACTACACAT[G/T]AGGTACAATATACAC	84708
rs555553222	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53584481	ACAAGCTTTGGAGGA[A/G]AGACAATAGAGAGTG	84708
rs555559099	in-del	-/A	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53494735	AACCCAGGGGTACAT[-/A]AGCAGCAGAACTTAA	84708
rs555560456	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53548877	ATGTCTTTCACAGGA[A/G]CATGGACGGAGCTGG	84708
rs555586173	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53483522	GAAACTCACATAAAT[A/G]GAGCTCTCTGGTGGC	84708
rs555616080	snp	A/G	0.00199481	0.0315187	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53595511	AAACTTCCAGGATAT[A/G]CCATTTCGGCAACCA	84708
rs555641286	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53587251	AACACAGAAAGTTTA[C/T]GGGAGACAACAAACG	84708
rs555642720	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53581668	CATGAGACTTACTCA[C/T]TATCGCAAGAATAGC	84708
rs555646951	in-del	-/AC	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53487872	GTATCTCAAAATGAG[-/AC]AGTTTGGCTTTAAAT	84708
rs555659672	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53587492	AGAGAGTCTATGTAA[C/T]GTCAGTACATAAATA	84708
rs555659749	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53490943	AAAGGTTTTTCCTGC[C/T]TATAAAGCACGTTGG	84708
rs555664206	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53476265	ATTGCACCACTGCAC[C/T]CTAGCCTGGGTGACA	84708
rs555681110	snp	C/T	0.00279162	0.0372561	intron-variant	LNX1	GRCh38.p7	4:53587917	GAGAAACAACACAAT[C/T]TTTGTTAACAGGTTT	84708
rs555710770	snp	A/C	5.54554e-05	0.00526542	missense, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573648	AGTGATGCTCGAGGT[A/C]ACAGCGCTGCAACAC	84708
rs555720484	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53627352	GTAAACTACTCATTA[A/G]CATTTGTAAGAAAAG	84708
rs555736564	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53481678	AGCCTTCCCAAGAAA[G/T]AGCCCCTTGCAGGAG	84708
rs555776942	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53646146	TTGTATTTCTATTGG[A/T]CTTATCATCCTATTC	84708
rs555789586	snp	A/C	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53539393	ATTTTTGAGACCTGT[A/C]TCACTCTGTCGCCCG	84708
rs555815719	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519134	TCACTGCCCCTCTTC[C/T]TCTCCAAAAATAATT	84708
rs555815824	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53526570	GCTTTTCCTTCCAGA[C/T]CCCTGTGCTACTCTG	84708
rs555824797	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53496800	AACAGCTCTTCAAGC[C/T]GAGTTGACATTTTCT	84708
rs555839084	snp	A/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53602622	GAATGGCCTTTACAC[A/G]TGGTGACTAAACTAA	84708
rs555863541	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53559799	ACTACAGGTGCGTGC[C/T]GCCATGCCTGGCTAA	84708
rs555905048	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53486748	GACTGGCTTTCTGTC[A/G]TTTTGTTTAATGACT	84708
rs555908053	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53512042	ACTCTCACTTTGGGT[A/T]CATTAATTGTCCAGT	84708
rs555928046	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53540307	AGGATGGCTTGAGCC[C/T]GAGTGGTTGAGGCTG	84708
rs555945763	snp	A/C	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53525812	GGCACTCTGAAGGCC[A/C]GGAAAGGGCTGTGTT	84708
rs555951793	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53475324	GTCATACTCTCTACT[C/T]TCACTCAGGCTCAGT	84708
rs555978181	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53614006	TTTTTGATAATAGCC[A/G]TTCTGACTGGTGTGA	84708
rs555983552	snp	C/G	0.0329836	0.124112	intron-variant	LNX1	GRCh38.p7	4:53565316	GAGAATGGGCAGACT[C/G]CCTCCTCAAGTGGGT	84708
rs555989981	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53636698	GGACAGCAGATAAAG[C/G]AGCCTCCACATTTTC	84708
rs555997564	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53641253	GGAGGGATTTCTAGC[C/T]ATGCAAATATATCCA	84708
rs555997941	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53633732	AGCGCCCTCATCCAT[C/T]TTCCTCCTCTGGGCC	84708
rs556002116	in-del	-/TC	0.00914312	0.0669923	intron-variant	LNX1	GRCh38.p7	4:53526643	GTATCTGCTTGAAAT[-/TC]TCTTTTTTCTGCTCA	84708
rs556027706	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53580172	TAGAGGAAAAAGTCC[A/G]CATAATGAGCAAAAT	84708
rs556042173	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53548753	AGCAGTATTCACAAT[A/G]GCAAAGATATGGAAT	84708
rs556063106	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53620860	AGGTATGCATGTGTT[C/T]GCCACTCAGGGAAGG	84708
rs556099201	snp	C/G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53592385	GGAGGCGTAAACTCA[C/G/T]CCAGCACCAGAGCAG	84708
rs556128602	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53476062	AGCACTTTGCCAGGC[C/T]GAGGCAGGCAGATTG	84708
rs556147822	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53553450	TTTGAAAACAAACTC[C/T]ACCCCTACTTCTGAT	84708
rs556149310	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53600315	ATGCACACAAAAAAA[A/C]GTCCTAGTAGGGAAT	84708
rs556153667	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53465687	TAAAAATTCTGATAC[A/G]TGTTTAAATTGTACA	84708
rs556158847	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53644923	AGCACAGTCAAAATG[C/T]GCTTCTCAGTTTTCA	84708
rs556186337	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53470614	TCAGCCCAAAATCTC[C/T]TTAAGCTGATAAGCA	84708
rs556186887	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53618200	AAGGAATTTTTCCTT[G/T]CAGCAGAGTTTTATG	84708
rs556193703	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53651640	GAATGGAGACAGGAT[A/G]TGCTGCTGGTCACCC	84708
rs556198387	snp	C/G	0.00318978	0.0398085	intron-variant	LNX1	GRCh38.p7	4:53470109	AAAATACTGGCAAAC[C/G]AAATCCAGCAGCACA	84708
rs556205129	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53623863	GTAAATGAGTAGCAA[A/G]GCTGGAAGTTAAACC	84708
rs556234239	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53599307	CCACCAAAACCAAGA[C/T]GGCTATGTGAGTAAC	84708
rs556247052	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53564802	GCACCCTGCGCCAGC[C/T]GAAGCAGGGCGAGGC	84708
rs556265605	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573553	GAAGCCCTCAGGAGA[C/T]TGGGGGGTGGAGGGG	84708
rs556272954	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53598776	AGTCAAAGCCTGAAC[A/G]CTTTGGGAAGGGAGC	84708
rs556289508	snp	C/T	0.00517822	0.0506191	intron-variant	LNX1	GRCh38.p7	4:53525092	AACCACAGGGCCTCA[C/T]GTGTATCATGCTCCT	84708
rs556305902	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53620726	AATAAGAAAAGAAAA[A/G]TTATATTAAATGTAT	84708
rs556311240	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53504241	GCATTTGCTGCTTCG[C/T]TACAATCAGCATCTG	84708
rs556318049	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53464995	TAACTTTTGCAGCTG[G/T]GCAATATCAAATTTA	84708
rs556319276	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53464959	CAGAACATTCTATAA[A/T]ATCTGTAAGATGTTT	84708
rs556343696	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53634921	TAGCTCACTGCATGG[G/T]CTTAATTGATCCTCC	84708
rs556346442	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53627259	ATGACCTTGGAGGTT[A/C]CCTGTTCACTTAATC	84708
rs556348289	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	LNX1	GRCh38.p7	4:53558232	GAGAGCAGGCAAGCT[C/G]ATGCCCAGGAAAGGA	84708
rs556349545	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507072	TTCTTCCTCATATGC[A/G]TAATGGTACTAGCGC	84708
rs556353878	in-del	-/T	0.473174	0.112665	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53505265	CTTTTTCAAGATAAC[-/T]TTTTTTTTTTTTTGA	84708
rs556355049	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53594695	TTTTACTTTCTTACT[G/T]TCTTTTCTTTCTTTC	84708
rs556363023	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53551065	GTTAGGTTAGAGTCA[G/T]TTAACCTAGGAGGCG	84708
rs556385484	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53647657	CAATTTTTAAGAGTA[C/T]AGTTCAGTAGTGTTA	84708
rs556391853	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53497177	TTTGTGCCTCACTAA[A/T]GATGTGTAGGGCTGA	84708
rs556394246	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53489726	TTTATCAAGAATGCA[C/T]AAAATTTGGAGCCCT	84708
rs556415782	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53606079	CACAGTTAGCAGAAG[A/G]CAGGAAATAATCAAA	84708
rs556420271	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498327	GAGAAAGAGGAGGTG[A/G]AGAAAGGGAATGAAG	84708
rs556425094	snp	A/C			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53522036	CTAGGCACAAGCAAT[A/C]CTTCCATCTCGATCT	84708
rs556461607	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53482962	TGTACATTGATATTT[A/G]GACAGGCATTCAGAA	84708
rs556484880	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53626495	TTTACCAAGTCTTTG[A/T]TGAGCATGCATTGAG	84708
rs556495572	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53594170	ATGTATATATAAATA[C/T]GTATATATTCATAAA	84708
rs556512478	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53540382	TGAGACCCTGTCCCC[A/G]CCTCCCCAGAAAAGA	84708
rs556513983	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53600889	GTGCCCACCACCACA[A/C]CTGGCTAATGAAACC	84708
rs556539914	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53639968	AACCCAGAGGCAGAG[A/G]TTGCAGTGAGCTGAG	84708
rs556565949	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53586448	GAGTTTCGACTCTGC[C/T]GCTGGTGAAGTCTTT	84708
rs556624082	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53556529	ACTGGATTTCAAAGA[C/T]CCCAACCTCAGCATC	84708
rs556640130	snp	A/G	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53464125	GAGAGCAGAAAATTG[A/G]AAATTGAATCTATAG	84708
rs556652572	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53645372	GATATTTGGTCATTG[C/T]CTTCCCTGCTGTGGG	84708
rs556657111	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53625630	AGTGACACCCTGTCT[C/G]TACAAAATAAAAAAA	84708
rs556667646	snp	C/T	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53630409	ACATTACCAGCAGAG[C/T]TCAGACAAGGTGACC	84708
rs556667848	snp	A/G	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53467690	CGAGAACTATGTGAC[A/G]AATGCACAAGCCTCA	84708
rs556705281	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53527585	CACTGCATTCATGCA[C/T]AGGAAATGCTTTGAC	84708
rs556732060	snp	A/G	0.00676609	0.0577691	intron-variant	LNX1	GRCh38.p7	4:53532382	CGGGAGGCTGAGGCA[A/G]GAGAATCACTTGAAT	84708
rs556766250	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53570984	GTGAGCAGAGATCGC[A/G]CCACTGCACTCCAAC	84708
rs556777971	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53499803	TCATGATCAAGAAGA[A/G]GCCAAGGCCTAGTTG	84708
rs556796785	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53486195	CTCTTTTCCGCCCTG[C/T]GCCAGTTCACCCCTC	84708
rs556796977	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53494452	TTGTCTTGTGTCTCC[G/T]TAGGATGACCCTTGC	84708
rs556801388	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53579269	CGTGTATGATGGGTA[C/T]GGTGGAAATCTTACA	84708
rs556809752	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53579515	TATAGAAGCTTCTCT[G/T]CCTAATTCTCAAATT	84708
rs556839180	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53536713	AAAGAGACTTTGATT[A/G]CACTAAGAAGCAGAA	84708
rs556842215	snp	C/T	0	0	intron-variant	LNX1	GRCh38.p7	4:53538774	GCAGCCATTAGTGTC[C/T]AGTCTCATTATTTTC	84708
rs556894304	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53529309	ACAGAATCTGCCTGG[A/G]AGCAGGCAGTGGGGA	84708
rs556939202	snp	A/G	0.000399281	0.0141238	intron-variant, synonymous-codon	LNX1, LOC101928879	GRCh38.p7	4:53575727	CAGTGTCTGCTGTGG[A/G]GGCCACAGCTCTGTA	84708
rs556950417	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461203	TTTACATTCTCCAAA[C/T]TCACTATCCATTCAG	84708
rs556952609	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53500920	TTTCCCTCCCTCATT[A/C]CCCTTCCCTTGTTAC	84708
rs556976315	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53582961	ATAATTCACCCAGCA[G/T]GCATGTCTGCCTAAC	84708
rs556981635	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53555625	GATTCCTTAGAGAAC[A/T]TGACAGTACCTGAAA	84708
rs556984818	snp	C/T	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53574688	CACTTTGCCTGGGTT[C/T]AAATCCCACCACTAT	84708
rs556992378	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53534501	AGAAAAAATTAGCCA[A/T]GCATTGAGGACATGC	84708
rs557018292	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53637337	TAAATGAATCTCTTT[G/T]TACCAACCACTGCTT	84708
rs557020705	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53628498	AAAAACAGTAGAAGC[A/G]TTGTGGATGTGACAA	84708
rs557036850	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53603162	TATTAAGGCAGCAAA[A/T]AAATCAGCCCTGGTT	84708
rs557056662	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53642854	CCCTCCCAGCCATGG[C/T]ATGGAAGCTCCCACC	84708
rs557066068	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53539508	GTAGCTGGGACTACA[A/G]GCATGTGCCACCATG	84708
rs557098694	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53479303	CTGTCATTTATAAAT[A/T]TCAGAAACTTTTCTA	84708
rs557100409	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53543765	TTGAGATCCATATGC[C/T]TCAATTCAACCCTGT	84708
rs557103892	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53515106	AAAGTCTAGTTCCAC[A/G]ATTACACCAGTAGAA	84708
rs557138235	snp	C/G	0.00438332	0.0466095	intron-variant	LNX1	GRCh38.p7	4:53471329	TCCTTACACCTTATA[C/G]AAAAATTAATTCAAG	84708
rs557161804	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53633865	AACCTTCTTAGGGCC[A/G]TGTTTCTGCATCACC	84708
rs557169762	snp	C/T	0.00279162	0.0372561	intron-variant	LNX1	GRCh38.p7	4:53465679	GAACTTTTTAAAAAT[C/T]CTGATACATGTTTAA	84708
rs557183244	snp	A/G	0.00557542	0.0525036	intron-variant	LNX1	GRCh38.p7	4:53568075	CAGAGGTACAAGGAG[A/G]AACTGGTACCATTCC	84708
rs557184706	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53583672	TAAAGGAGGACATAG[A/T]TGTTCAGAATGTGGG	84708
rs557220851	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53628841	TGACTTGGACGAAGC[A/C]GGAGGCCATTTTTCT	84708
rs557227312	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53602509	AGCTGCACCTTGAAG[G/T]GTGGCTTGCTGCAAA	84708
rs557246306	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53567522	GAAATTTATAGCACT[A/G]AGTGCCCACAAGAGA	84708
rs557247734	snp	C/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53554968	GTCTGAGCTGGGCAT[C/G]AACTCAGGAACACAA	84708
rs557270440	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53630806	GGTAGTTCCTCTAGG[A/G]GCAATGATTCAGAAT	84708
rs557280129	in-del	-/T	0.0130921	0.0798413	intron-variant	LNX1	GRCh38.p7	4:53562466	AAGAGCTCTCTAGTC[-/T]TGAAGACAATCAATG	84708
rs557309076	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53648491	TAGGGGTTCTTTACA[C/T]ATTCTGGATATTAAC	84708
rs557322863	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53543183	TACTGTTATCCGAAG[A/G]TCAGTTGCCCTCATG	84708
rs557333211	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53629498	GTTCATCCCAGGACC[C/T]GGAGAGAAAGTATGT	84708
rs557340190	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	LNX1	GRCh38.p7	4:53653500	ATAGAGTCCAGGTAC[G/T]TGTGGCTGCCTAATC	84708
rs557357001	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53499217	CTCTGTTGCCCAGGC[A/T]GGAATGCAGTGTCTC	84708
rs557357593	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53615125	CACAGGAGAAAAATG[C/T]CACGATTGAAACAGT	84708
rs557362276	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53609290	GTAAAAAAAAAAGGA[A/T]ATCTAAAGAGAAAAA	84708
rs557373561	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53478459	AAAGTCCTGGCCGAT[C/G]ACTCCCACATTCTCT	84708
rs557376105	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53582005	ATTAGGATTACTGAA[C/T]TTTTCTGCACCTTAA	84708
rs557420772	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507175	ACATACGTGAGAAGT[A/G]GGCTAATCAAAGTAA	84708
rs557432164	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53502771	GTTTTATCAACTATG[C/T]TTATGTAATATTCTC	84708
rs557444500	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53492127	TCTGGCAGGTAATAT[C/T]AGTTGGTAGTAATTG	84708
rs557461780	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53601896	GTTACTGCTGTTTCT[C/G]CCTGCCCTGCATCCC	84708
rs557498663	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53642494	GATGGGTCCTGAGGG[A/G]CCAGCACCAGCTAGG	84708
rs557504224	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498938	TCAGCCAAACTAAAC[C/T]ATTCATTTTTCCTCA	84708
rs557512646	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53623980	GGTAGTTATTCCTCA[A/G]AAGAATATAGGTTTT	84708
rs557526659	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53572701	ACATGACAATGTAAG[C/T]GGACAAAATGAGAGG	84708
rs557549062	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53630290	GTTATGAATTTAGCT[A/G]CTTGCTAAAATTTTT	84708
rs557550950	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53623546	GACTCAAGAACAATT[C/T]TGATGCAAACCATAA	84708
rs557562895	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53514419	AGTCCCACCTGGCTG[A/G]GGAGGCCTCACAATC	84708
rs557564441	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	LNX1	GRCh38.p7	4:53654120	TATTTACTGGAGTTA[C/T]GGTAACAAAGAGAAA	84708
rs557570084	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53513693	TCCAACTACTTTTCA[A/T]CATGGCTACTGCCAC	84708
rs557587503	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53642542	CTGTACACTCTAAAG[G/T]CATATGTGGCACGGT	84708
rs557587691	snp	A/G	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53629778	CCTGGAAAATGTGGA[A/G]GCCAACACCCCTGAC	84708
rs557592592	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53466735	CCAAGGAGCCTTGCT[C/T]ATTGCTAGCACAGCA	84708
rs557644275	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53608389	CACTGATTACAGAGA[A/G]ATGCAAATCAAAGCC	84708
rs557674339	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53628221	ACAACCCACAGAATA[C/G]GAGAAAATATATGCA	84708
rs557686801	snp	C/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460150	CTCATGACCATGTCT[C/G]TGAGCCAGGGTCAAG	84708
rs557691959	in-del	-/T	0.00119737	0.0244387	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53506058	TGAATTTTGAGGGCA[-/T]TAATACATACAGTGG	84708
rs557695199	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53530525	AAAGATCTTCAGTGA[A/G]ACACTTCATAAAAGC	84708
rs557705093	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53485295	GGATCCCAGCAGAGT[A/G]TCCATAGGCTTGCAA	84708
rs557715911	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53615988	TGCTATCAAATAGCA[A/G]GTCTTACTAATTCTT	84708
rs557723085	snp	A/G	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53477226	TTACACAAGAATACC[A/G]CTGAAGGAAGGAAGG	84708
rs557726229	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53520442	GTCAATTCTTCAGAG[A/G]CGCCAGAATCGTTTG	84708
rs557730673	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53586934	TGAGATCATTAAGGT[A/G]ATCTTCACTTTACAG	84708
rs557745949	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53467177	GGCAGCAGCATTTGC[A/G]TTTCACCAATATCCA	84708
rs557757964	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53553594	CCCATGATGCTGAAA[A/G]TTATTTTCCCAGATT	84708
rs557773897	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53580992	CCACTGACATTCACT[A/C]TAAATGAAAAAGTTT	84708
rs557783476	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53548957	CATATCTAAGTGGGA[C/G]CTGAATGGTAAGAAC	84708
rs557789890	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53548303	GAAGTTGTTTTACCA[A/G]TGAGCCCTGAAAGTG	84708
rs557792693	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53641879	CTTTTTTTCTGCTTA[A/G]TATTGCATTGTGTGG	84708
rs557820449	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53542861	CTCTCCCATCAGGAA[G/T]AAATCAGGGGGAAAG	84708
rs557844238	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53483699	GGTTCCTCTCTTCAT[C/T]CCATCCCTTGCCCAC	84708
rs557853112	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53554326	CTGGTGTCTTTCCCA[C/T]TGGAGTCAATAGGTG	84708
rs557909906	snp	A/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53486082	GAATCCTAGATTGTG[A/T]TCTAGGCAAATTCTG	84708
rs557910653	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53510249	CTAGTTCACCAATCT[A/G]TGCATCATGGGGATA	84708
rs557918467	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53608125	GACACATGGGACCTA[C/G]TTAAACTAATGAGCA	84708
rs557921518	snp	C/T			synonymous-codon, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460967	TCCTTTAAGTTCTTT[C/T]AGCAGTCTTGCCAAG	84708
rs557929711	snp	G/T	0.00517822	0.0506191	intron-variant	LNX1	GRCh38.p7	4:53470752	CAATTGCTTCAAAGA[G/T]AATAAAATACCTAGG	84708
rs557931693	snp	A/G	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53477111	GTTTTCTTTGTTGAC[A/G]GGAGGCTGGGTGCTC	84708
rs557941514	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53633514	ATCCTTGTTCCGTGG[G/T]CTATGGCCAGGGAAG	84708
rs557956554	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53542519	TTGATCTGAATCAAT[A/G]CTCTGACTGATGACC	84708
rs557959532	snp	C/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53478008	GACAATATTATTAAG[C/G]ATACATATTTGTAGA	84708
rs557964957	in-del	-/A			intron-variant	LNX1	GRCh38.p7	4:53570415	AACTATCACAAGAAC[-/A]AAAAAACCAAATACC	84708
rs557994266	snp	A/G			nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53604388	TGCTTGGGGCAAAGG[A/G]AATGTTTGGAGAAAA	84708
rs558037956	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53581561	CCTCACAATCATGGC[A/G]GAAGGTGAAGGAGGA	84708
rs558040669	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53520352	CAACTCAGAATTCCA[A/G]AGCCACAACCAGATG	84708
rs558111945	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53566700	CTAAAAGACACAGAC[G/T]GGCAAATTGGATAAA	84708
rs558116584	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53621879	CATTTCACCCCCACC[A/G]GATTTGTTGCCTCAT	84708
rs558141078	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53636398	GATCACAGGAGAAAT[A/G]CTGGCAGAGGAACTG	84708
rs558147598	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53463786	ATGAGTTAATAAGTA[C/T]GCTGAAGTCTTGAGC	84708
rs558156177	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53648769	TAGACTTTCAGAACA[C/G]TTTCAAAAACTCCCT	84708
rs558184038	snp	G/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53491000	TTAGGAAGTCCCAGT[G/T]TTAGGCAAGGTTTTA	84708
rs558200908	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53628180	CAGGTAAGACTCTTC[C/T]TGAAAATAATCATCA	84708
rs558212499	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53532908	TGTTCCAAATATTTC[C/T]TCCTCTGGGAGCCTG	84708
rs558237653	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498221	TAAATAAAATACAAA[A/G]TGTTCTATTAATCTA	84708
rs558237753	snp	C/G	0.00636936	0.0560724	intron-variant	LNX1	GRCh38.p7	4:53634887	CTGTCACCCAGGCTG[C/G]AGTGCAATCATGGGA	84708
rs558243076	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53488601	TGGCGTTTCAATTTT[G/T]TCATTCATACAAGCA	84708
rs558258741	snp	C/T	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53544202	TTTCTCTCTCTCTCT[C/T]TCTTTTTTTTTTGAG	84708
rs558266110	snp	G/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53539426	TTGGAGTGCAGTGGT[G/T]CAATCTCTGCTCACT	84708
rs558277166	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53651313	TCCTGCTCTGCACTG[C/T]GTCAGCATTCCTTGG	84708
rs558301253	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53497481	TCATGCAAAGGCAAA[G/T]CTCACCACCTTTGTC	84708
rs558311910	snp	A/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53521949	GGACTACAGGTGTAT[A/T]CCACCACACCTGGCT	84708
rs558320314	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53468896	AATAATAATGGGAGA[C/T]TTTAACACCCCATTG	84708
rs558332415	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53474059	TGATGCAATGCCTAT[A/G]TAGTCCTATAGGAAT	84708
rs558334148	snp	C/T	0.00795532	0.062565	intron-variant	LNX1	GRCh38.p7	4:53468499	ACATAACAATATTCA[C/T]CTTAAATGTAAATGG	84708
rs558373168	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53638329	CAAGACTGTACAATA[C/T]AGGTATAGTCAATTG	84708
rs558380365	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53647751	CTCGTCACCCATTAA[A/G]CAGTAACTCTCCATT	84708
rs558384983	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53565379	GGAGGCACCCTCCAG[C/G]AGGGGCACACTGACA	84708
rs558391690	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53583801	AGAAGAGTGTTCCTT[C/T]TCTTGACGAGATTTT	84708
rs558402273	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53571526	AGCCAAGGAAGACAG[A/G]CAGCACTAGAAGCTG	84708
rs558424845	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	LNX1	GRCh38.p7	4:53652599	AGATGTTGTTTCCTG[A/C]AGGCAATGGGAAAAT	84708
rs558437457	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	LNX1, LOC101928879	GRCh38.p7	4:53578001	TATATTATGTTATTC[A/G]ATCCTCACAAATGGC	84708
rs558442873	snp	A/G	0.0103295	0.0711199	intron-variant	LNX1	GRCh38.p7	4:53570824	CGAGGTCAGGAGATC[A/G]AGACCATCCTGGCTA	84708
rs558507589	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53555813	TTCCCTAGCATCATA[A/C]TTTTATAGATTGCTT	84708
rs558525720	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53649830	TCTGCTTCCCACAGT[A/G]GACTGGGAGTTCCTT	84708
rs558535558	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53622622	CAAATCCTCTTATTA[C/G]AACAGGATACAGTAA	84708
rs558535586	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53526895	TCCACAGAAGGCTCA[C/T]GATGTTTATAAAATT	84708
rs558537052	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53481097	AGAAGTACAAATTGG[C/G]CTGAGTCACTTCATT	84708
rs558538667	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53537340	CCTTGGGTCCACCCT[C/T]TCTTAATTGACAATG	84708
rs558556152	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53618638	AAGACACTCACCCTG[C/T]TGGGGAGGGCCTTGA	84708
rs558567210	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53488053	TTCCATAAAATTAGA[A/G]AGTCACAGACACACA	84708
rs558567977	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53625549	CACCTGTAATCCCAG[C/T]ACTTTGGGAGGCCAA	84708
rs558593256	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53625048	GATATTTTTAAAACT[C/T]GTAGGCACATTGTAC	84708
rs558596305	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53645178	ACACTCCGGGATACA[C/T]GGTGGCCCTTACACA	84708
rs558606658	snp	A/G	0.00438332	0.0466095	intron-variant	LNX1	GRCh38.p7	4:53584243	TTCTCAACATTTTCC[A/G]GCTGTGTTTCAATTC	84708
rs558610976	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53619751	ATGTGCTGGGTTACA[C/T]GGTAATTCTATGTTT	84708
rs558643483	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53590455	GCAGCTGGGCTTAAA[A/G]ATGGTTTCCTTTCTC	84708
rs558653294	in-del	-/T	0.00318978	0.0398085	intron-variant	LNX1	GRCh38.p7	4:53609788	ATATATAATATATTA[-/T]TTAAATATAAAATAT	84708
rs558663938	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53631794	TGGCTGCAAACAGTC[A/T]CCCCAGGGACATGAA	84708
rs558670394	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53467770	AATGAATGAAATGAA[G/T]CGAGAAGAGAAGTTT	84708
rs558675823	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53529034	TACAGGGGTGTCTGG[A/G]GTTTTCAGTTCATGA	84708
rs558690351	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53610254	ATAAATAAGAAAAAA[A/T]TATCAAAAGGTAACA	84708
rs558715744	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53543424	ACATTTGATAAGTAT[C/T]TGTTATTAAATTATA	84708
rs558717631	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53550620	GAAATGGATGCTAAG[A/G]CAATCCACTGTATTC	84708
rs558730131	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53550170	CAATGTAAATGAATG[A/C]GGGCCATGCGGCTTC	84708
rs558748116	snp	A/T	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53644293	GTAGCCCTAGCTACT[A/T]GGGAGGCTGAGGCAC	84708
rs558748777	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53517337	CTCCTTTAGTGAAAA[A/G]CACTAGAAATCTTTA	84708
rs558779672	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53644969	AGTAGTACCTTAGCC[C/T]CAGCCCTGAGACCTA	84708
rs558783266	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53643806	GACTTTTCAGAATTA[C/T]GAAAATTAAACAAGA	84708
rs558816611	snp	G/T	0.00318978	0.0398085	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508311	TCAAATACAATTGAA[G/T]AATGTATAATAGGCT	84708
rs558826842	snp	A/G	0.00358779	0.0422022	intron-variant	LNX1	GRCh38.p7	4:53538654	TTCCCCATGTAGCCT[A/G]AGTCTCACTTGATTC	84708
rs558867281	snp	C/T	0.00199481	0.0315187	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53516646	GCCAGGAATGGTAGA[C/T]TCTGGGCAGGTTTTG	84708
rs558879459	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53523621	ATGATATGCACATCT[C/T]ATGTGAAATCAGATA	84708
rs558890072	snp	C/G	0.00358779	0.0422022	intron-variant	LNX1	GRCh38.p7	4:53560332	CTTGCATTTAAAGGG[C/G]ATGAAATTAATTAAT	84708
rs558892541	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53650479	GGCTTCTGATGAATG[C/T]CAGAGAAGGGAGTTA	84708
rs558936564	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53619163	AATAACATTAGATGG[C/G]CTTAATTTTTTTTAC	84708
rs558962651	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53603276	ACTCATTTTCATATT[C/T]ATGGTTCCTAGCTCA	84708
rs558975378	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53485443	AAGGAGAAGCCTGCA[A/G]GAACTATTTAATTCA	84708
rs558980141	snp	A/G	0.0107246	0.0724382	intron-variant	LNX1	GRCh38.p7	4:53472258	AACCAAATACTGCAT[A/G]TTCTCACTCATAGGT	84708
rs558989545	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508596	TATTTTGACCATGAA[A/T]GCCCTTAGTCACACC	84708
rs558994653	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53471810	TCACACCAATTAGAA[C/T]GGCGATCATTAAAAA	84708
rs559011838	snp	C/T	0.000365376	0.0135113	missense, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461529	CATAACCTCCTACAA[C/T]GCAGAAGCCCAGACT	84708
rs559019849	snp	C/T	0.000399281	0.0141238	intron-variant, synonymous-codon	LNX1, LOC101928879	GRCh38.p7	4:53575743	GGCCACAGCTCTGTA[C/T]TGCATCATCCTGGTG	84708
rs559049835	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53533528	CTCAGCCTCCTGAGT[A/G]GCTGGGACTACAGGC	84708
rs559062892	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53527296	TTTTTCTAAGACAAG[A/G]ATTATTTATTCAGTA	84708
rs559088453	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508788	CATTCTCTTTCTCTG[A/G]GCTGGTCTGGGAGGG	84708
rs559096611	snp	A/G	0.000399281	0.0141238	nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53604201	CGTAGAAGACAATTT[A/G]TATTACTCTTTCCCT	84708
rs559099148	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53526010	ATTTAATCAATAACT[G/T]GTTTATTGACATTCA	84708
rs559103245	snp	C/T	0.000399281	0.0141238	intron-variant, missense	LNX1, LOC101928879	GRCh38.p7	4:53575680	ATCTGGGACCCACCC[C/T]CTGGGCTGGCTAATC	84708
rs559109350	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53616312	CCATACACTTAAAAG[C/G]TCATAGGAGACAAAA	84708
rs559114644	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53531233	AAGTGCTGTGGACAT[C/G]AGGTGGGGAAAGAAC	84708
rs559117624	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53568453	ATTCAACAACCTTTC[A/C]TGCTAAAAACTCTCA	84708
rs559128764	snp	A/G			intron-variant, downstream-variant-500B	LNX1, LOC101928879	GRCh38.p7	4:53577809	CCACCAGACTAGATC[A/G]TGTACAACAGTCCCT	84708
rs559134004	snp	A/G	0.000399281	0.0141238	nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53603596	CCTCAGGAAGCTTCC[A/G]ATCATGGCAGAAGGC	84708
rs559134302	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53611154	AGAATTTGATAAAAT[A/T]GGTGGATCTACAAAC	84708
rs559151197	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53505289	TTTTTGAGATGGAGT[C/T]ACCCAGGCTGGAGTG	84708
rs559205248	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53515783	ACGGAGGAAAAAGCA[A/C]ATGCTTTCACTTCTA	84708
rs559245128	snp	C/G/T	0.000131805	0.00811706	missense	LNX1	GRCh38.p7	4:53478685	TGCCGAGAGATTCAC[C/G/T]GGGGTCTTTTTGGAT	84708
rs559250460	snp	A/C	0.00159617	0.0282053	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53516003	TGCTTATAATCCTAG[A/C]GCTTTGATAGGCTGG	84708
rs559265166	snp	C/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53549870	TTACGGACATCCCAG[C/G]TTTGCCTCTTATCCG	84708
rs559271637	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53610503	ACGAGGTCAGGAGAT[C/T]GAGACCATCCTGGCT	84708
rs559286908	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53617002	TCATTTGTACTTCTC[A/T]TTAGCCAAGAAACAA	84708
rs559314191	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53515156	GAGCTCTCTCTCCAG[A/G]ACTGAGATGGCTTCC	84708
rs559343587	snp	C/T	0.000798403	0.0199641	intron-variant, stop-gained	LNX1, LOC101928879	GRCh38.p7	4:53575773	GGTAGTCACAGTGGC[C/T]GAGTGAGTTTCTTGG	84708
rs559380471	snp	A/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53560127	AGTTTCACAAAGTCC[A/T]GAAACATGCTCTTCT	84708
rs559398139	snp	G/T	0.00119737	0.0244387	upstream-variant-2KB	LNX1	GRCh38.p7	4:53653019	TTCTTCTGCTCATTC[G/T]TCAGCATCACCATCA	84708
rs559411305	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53471574	ACAGAATGGGAGAAC[A/C]TTTTTGCAATCCACT	84708
rs559421171	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53554838	GCCTAGGCAACAGAG[C/T]GAGACTCTGTCTCAA	84708
rs559434910	snp	C/T	0.000798403	0.0199641	utr-variant-5-prime	LNX1	GRCh38.p7	4:53652281	TTTTCTTTCTCTTTC[C/T]AGTGTTCTTCGTCCC	84708
rs559440290	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53632054	TCTTCTAATCCATTG[A/G]ATCTTGACCTGGAGT	84708
rs559453643	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53535889	TGACCCCTGATAACT[A/G]TTGACAAAAGCACCA	84708
rs559478259	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53589048	TGGTTAGGGAGAAGG[A/G]TGTTTATCTGTGAGA	84708
rs559495625	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508418	TGCCAACCAAGTGAA[C/T]TCATAATTTGAGATT	84708
rs559531437	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53647895	GGCTTTATTTCATTC[A/G]ATATAACATCCTCAA	84708
rs559535930	snp	A/G	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53466540	AAAGCAGGGCAAGGC[A/G]TCGCCTCACCCGGGA	84708
rs559548543	snp	G/T	0.0275645	0.114116	intron-variant	LNX1	GRCh38.p7	4:53470838	CTCAATGAAATAAAA[G/T]AGGATACAAACAAAT	84708
rs559561168	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53472050	CACTTATGTTTATTG[C/T]GGCACTATTCACAAT	84708
rs559572807	snp	A/G	0.00438332	0.0466095	intron-variant	LNX1	GRCh38.p7	4:53556478	ACGAAGAAGGATAGC[A/G]CATGGGAATGGGTGG	84708
rs559588002	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53555099	AGCTCGGATAAAGGG[C/T]GGAGGAAGCCCAGCA	84708
rs559611952	snp	C/T	0.00676609	0.0577691	intron-variant	LNX1	GRCh38.p7	4:53565896	TGGAAGAAAGGGTAT[C/T]AGCAATGGAAGATGA	84708
rs559615340	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53588460	CACATGGTAGATCTG[G/T]GTTTCAAAAACCCAG	84708
rs559618587	snp	C/G	0.00795532	0.062565	intron-variant	LNX1	GRCh38.p7	4:53569931	CTCACCATCACTGGC[C/G]ATCAGAGAAATGCAA	84708
rs559625776	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53649912	CTGGAACCTCGTAAG[C/T]GCTTTGTATCTGTTG	84708
rs559684108	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53466931	GGCAGGGCACAGACA[A/G]ACAAAAGGCAGCAGT	84708
rs559699622	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	LNX1	GRCh38.p7	4:53654471	TTTCTCCTTTCTCAT[C/T]TGCGAGCAACCGGAT	84708
rs559701764	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53551509	ATATGAATCCTCAAC[C/T]GATAAGGAGAAAAAG	84708
rs559765618	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53548637	CTCAAAGAGCTAAAA[A/G]AAGAACTACCATCCC	84708
rs559770346	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53557385	TTCAAAAGCATCAAA[A/G]ATAAAAATAACATGG	84708
rs559787647	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53499515	CTGAGGGCATAAACT[C/T]TCGCTGTTCCATGGT	84708
rs559794231	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53650708	ACCTCTGTCCCCTTC[C/T]GTGTCCCCCCAAGAA	84708
rs559801043	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53574860	TAATTCTTACATGTA[C/T]TTGTTACTGAATTCA	84708
rs559825180	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53650369	AGGGTGCGGAGGGCA[C/T]CTGCATGGGCAGGGG	84708
rs559832014	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53563871	CTTGCCAATAAAATG[C/T]CAAGGGGGTGGGAGG	84708
rs559842152	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53527458	CATAATTAGTCTCTA[C/G]GAGCCTGGTGCTGAC	84708
rs559845587	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53547125	AAATCGAAGACTATG[C/T]CTATTGTGAGGCGCA	84708
rs559856788	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53464431	AAAATGAAATATTTA[C/G]CTCCAATTTTTATTG	84708
rs559863570	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53523858	ACACTGTCCCACCAT[C/T]CTCCTGCTTCCCCTG	84708
rs559866295	snp	A/T	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53513253	GCTCATATCTATTGA[A/T]CTTTTTTAATGTATT	84708
rs559891916	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53589782	TGTAAATTACCCAAC[A/G]GACCAACTGCATTCT	84708
rs559893103	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53468994	ACCAAGCAGACCTAA[C/T]AGACATCTACGGAAC	84708
rs559907905	snp	C/T	1.64991e-05	0.00287215	intron-variant	LNX1	GRCh38.p7	4:53476735	ACGCCCCTACAGGGA[C/T]GTTGTGTTTGGACTT	84708
rs559926496	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53499888	GGAGATTCAAAGATC[A/G]TCTAGGCTGGTGTTT	84708
rs559936452	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53615305	TGAGGCTGCTTCTCC[C/T]AACAGGAGGCAGGGA	84708
rs559943492	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53627311	TACAGGGTGGTCCTC[A/C]GTATGTGTTTATCTT	84708
rs559963691	snp	C/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53642577	CTTTATATGCTTGGG[C/G]TCAAATCAATGCTAC	84708
rs559970531	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53517495	ACTCAAGTAACAATA[A/G]TACAACTTCTATTCA	84708
rs559985881	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53552380	AATTTTCAAGGATGA[C/T]AGGAACTAAAAGTTT	84708
rs559998483	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53571674	ACAAATTTGTTTTTT[C/T]CTTTTTTTGAGACAG	84708
rs560018142	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53636903	ATCTGTTTGGAGTGA[A/G]GGTGTTATACACTTA	84708
rs560018681	in-del	-/TT	0.00398564	0.0444627	intron-variant	LNX1	GRCh38.p7	4:53525996	AGTATCTAATTACTA[-/TT]TAATCAATAACTTGT	84708
rs560020596	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53578567	CATGTCGTTATGGGG[A/T]CCATGACTGTAGATA	84708
rs560029481	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53602629	CTTTACACGTGGTGA[C/T]TAAACTAATGAAGTA	84708
rs560035143	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53612536	TATGATGGAAAAATA[C/T]AGTCATTAAGAATAA	84708
rs560039761	snp	C/T			intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461827	AAACTGACAGCCCTA[C/T]TGTGTTCTGTTACAC	84708
rs560098331	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53545836	TTTTTGAGACAGGGT[A/C]TTACTCTGTCGCCCA	84708
rs560103362	snp	A/C			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53511609	TCTTTTATCAAAGTG[A/C]GTAGAGGTAAATCTG	84708
rs560134778	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53645075	AAGGGCACAGCCAGG[C/T]AGTGTCCACGCCAAA	84708
rs560143647	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53631345	AGAAGGGAACTTCCC[C/T]GTGGGCCTTCAGCAG	84708
rs560155037	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53640136	AAAAATAGAATGACA[A/G]TGGTGGTGGGAGTAT	84708
rs560156130	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53468603	GGAAACCCATCTCAA[A/G]TGCAGAGACACACAT	84708
rs560184718	snp	C/T			nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53605087	GAACTGGCATAGCAC[C/T]ACTTCTCCCATGTTC	84708
rs560207089	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53502274	GGTCATTAATTTATA[C/G]TTCATTCTTCATAGT	84708
rs560226897	snp	A/C			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53520057	TTGTGGATGTTCTGT[A/C]CCCACGTTTAGTAGA	84708
rs560229023	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53606940	CCTCAACAAACTGGG[C/T]ATTGAAGGAACATAC	84708
rs560232951	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53516811	TCCTAAACCATGCCC[A/G]TGGGGGTAAGAGACA	84708
rs560233123	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53471743	ATGAAAAAATGCTCA[C/T]CATCACTGGCCATCA	84708
rs560247211	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53590827	AAGAGCAAAGAAAAT[G/T]GTAGACTTTTTCAGA	84708
rs560253673	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53474232	TTTTTAAATAAAATG[C/T]ATGGTACATAGGAGT	84708
rs560266099	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53510527	TCGTGAGGTTTTACT[A/G]TACCGATTAGCTGCG	84708
rs560282714	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53582693	TAGCTTCAAGAAAAT[A/G]AGCTTAAGATTTTTT	84708
rs560290042	snp	A/G			intron-variant, missense	LNX1, LOC101928879	GRCh38.p7	4:53576266	TGAAGCTTTCAGATG[A/G]GTTAGCATACCGCTT	84708
rs560306251	snp	A/C	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53538471	GGCATGAGACTAGGA[A/C]CCCTGCTTTTTTGAA	84708
rs560389505	snp	A/C	4.94303e-05	0.00497119	missense	LNX1	GRCh38.p7	4:53496268	TGTAGGCATCCGGGG[A/C]CTGTCCATTGTTCCT	84708
rs560391562	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53585171	ATACTATGTGTTTAC[G/T]AATGCAATCTATGAT	84708
rs560400022	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53639770	GGTGTAGTGGCTCAT[A/G]CCTGTAATCCCAGCA	84708
rs560447507	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53530158	AATAGTTGTGTTAGA[C/G]CAATTTGGTTATAGA	84708
rs560456173	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53632896	AGGTTTCTTTCTTAC[C/T]CCCCTCCTCCTGATT	84708
rs560458646	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53622736	TAACACAGTGCAGTT[A/G]CTTGTGTTTATTGGG	84708
rs560466820	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53504008	GGCATAGTGGTGCAC[A/G]CCTGTAATCCCAGCT	84708
rs560474774	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53599698	CAGGTCCCCCACAGC[C/T]TTATCTTGGCTCTTA	84708
rs560479637	snp	A/G	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53583914	CATAAACATGATGAA[A/G]TAGAACTGACCCCCT	84708
rs560546437	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53581421	CATCATTTTTTCCAA[A/G]AACCTTCCTCTTTGC	84708
rs560555729	snp	C/T	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53615260	TGCAGCAGTAGTTGG[C/T]GAATGCTGTGTGTAA	84708
rs560576966	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53488297	TGCCTATTGGTCTAG[C/T]TATGCCCAGTAGGGC	84708
rs560595747	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53468314	TTTTGTCACCACCAG[A/G]CCTGCCCTAAAAGAG	84708
rs560610068	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53562527	TCCTAAATGTTTTGC[C/T]CAAGTATTTATATTT	84708
rs560639064	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53644013	ATTTACTCTAAAAGT[C/G]TTATTAATAATAATC	84708
rs560644369	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53473693	GGATCAGCAAATATA[A/G]CTAATGAGTACTAGG	84708
rs560658650	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53537500	GCTTTATTCCTTTTA[C/T]AGCAATACACAGTGA	84708
rs560673034	snp	A/T	0.00716266	0.059414	intron-variant	LNX1	GRCh38.p7	4:53570326	ACACCATGGAATACT[A/T]TGTAGCCATAAAAAA	84708
rs560704037	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53591869	CACCAAAATGAGACA[A/G]TAATTTAGCAGACAC	84708
rs560720682	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53612011	TCATTTTTATAATAT[A/G]CAAAGATTTGTTATG	84708
rs560726624	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53638002	AAGAAATGATTTATC[A/C]CTGATAGATGGCAGC	84708
rs560767495	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53571069	TTTGAGATGGAGTCT[C/G]GCTCTGTCACCTAAT	84708
rs560778073	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53480537	AGATGATCAGTTAAA[C/T]TTAAACATTAAGCAT	84708
rs560782174	snp	G/T	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53570894	TAGCTGTGCGTGGTG[G/T]TGGGCACCTGTAGTC	84708
rs560786672	snp	C/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53584492	AGGAGAGACAATAGA[C/G]AGTGCATGTGGCCCA	84708
rs560786725	snp	A/T	0.00676609	0.0577691	intron-variant, utr-variant-3-prime	LNX1, LOC101928879	GRCh38.p7	4:53576648	AAAATAAATTAAAAA[A/T]AAAAGAATCCTGCCT	84708
rs560791287	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53464252	ATTAACTTAATAGAT[A/T]CCAGTGAGTAATGTA	84708
rs560799695	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53649327	AAGAATTTAATTTAC[A/G]TGTCAATCCCACAAG	84708
rs560801385	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53650065	CAGCCCACATCCATA[C/T]AGATGAGCAGACCGA	84708
rs560821586	snp	A/C	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	LNX1, LOC101928879	GRCh38.p7	4:53577388	ATTCAGGCTGCAGTG[A/C]GGCCATACCACTGAA	84708
rs560825844	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53516772	TGATGGCCAGTCCAT[C/G]TACCTACTTCTGGGG	84708
rs560829011	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53463446	TATGTTAATCTGTTT[C/T]AAAGTCATACCTTGG	84708
rs560841227	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS2	GRCh38.p7	4:53591132	TAATCAGATCAAGTA[C/T]GAGGACAAGCACAGG	84708
rs560854953	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53487161	AAGTCAAACATGCCA[A/C]CACACAAGGAGCAGC	84708
rs560887259	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53516086	TTCTACAAAAAAATT[A/T]AAAAAATTAGCTGGG	84708
rs560888943	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53503920	AGGCGGATGACCTGC[A/G]GTCAGGAGTTCAAGA	84708
rs560893297	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53525731	AGGGGAGGTTCTTCT[G/T]GGATCAATGCTATGG	84708
rs560921665	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53545115	CCTTTGTAATCTTTC[A/G]TCAATTAGCTCATGC	84708
rs560926648	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53557356	CAAGGCATGTTTCTT[C/T]GTATCCCATAGGTTT	84708
rs560928132	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53467409	AACAGAGCAGAAAAA[C/T]CAGAAACTATAAAAA	84708
rs560936026	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53551460	TGGACTCAAGCATGC[A/G]CACTAAGAGGCAAAA	84708
rs560945477	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53637959	GAGAGAAGGCTCCCA[C/T]TGTGTATTCTTGAAA	84708
rs560954558	snp	A/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53552983	TCATTATGAGCAAGG[A/T]CAATATTCCCTTCCG	84708
rs560972392	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53637553	CTGTGAAGTTGTAGC[A/G]TTGCTCAATCCCCAC	84708
rs560982174	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53643907	TTATTATTTCATGAA[C/T]GGAGCATGACCTGAC	84708
rs560996453	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53486113	GACACACTGGTTACA[A/G]CCTGCATAGCTTGAC	84708
rs561005785	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53611303	TGCACAACAAAGTTA[C/T]ACTAAAATATGCAAA	84708
rs561013177	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53598928	CATTTGAGGAACTTA[C/G]AGTCAATAAGGAAGC	84708
rs561014120	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53465088	GCGTCTTGCATTTTG[A/C]CCTTTGATGTTATTG	84708
rs561034730	snp	A/C/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53512141	GCCATTGGGGACCAT[A/C/G]GTGAGCAGTGCTGCT	84708
rs561051360	snp	A/G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53632852	ACTAGATTTTCAGGA[A/G/T]TCATTTGTTTCTCCA	84708
rs561057737	snp	A/C	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53479505	ACCAGTGTCCATGAC[A/C]ATTTCCTTTCTTAAC	84708
rs561071201	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53544490	TGAGCCACCATGTCC[A/G]GCCTGAGAGGTGCTG	84708
rs561078393	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53597183	TGCTTTGCAATGCTA[A/G]CTGCACTTGTCACTC	84708
rs561093008	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53639684	GCCCACTTACCAGCT[A/G]TTCATATCTCATGAC	84708
rs561107250	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53495823	TGCTGGGATTACAGG[C/T]ATGGGCCACCACGCC	84708
rs561114227	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53630595	AAGGCTGTGATGTAG[C/T]TTCCAGAGAAAATAC	84708
rs561119692	snp	A/G			intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53499429	CTCCCAAAGTGCTGG[A/G]ATTACAGGTGTGAGT	84708
rs561151342	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53536962	AAATATCTCTGACTT[A/G]GTGTTAACAGTGATG	84708
rs561210660	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53551114	TGGTTCTAAGAGCTT[G/T]GTGTGTTCTGTGGCT	84708
rs561211745	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53510439	CCTCATCTTCTAGAT[A/G]AGAAAACAGGCCTCC	84708
rs561213270	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53543556	CACTATACAAAGAAA[A/G]CGCTGAACAGAGAAC	84708
rs561220805	snp	G/T	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53503277	GGTGAATCCTTTCCA[G/T]AAGGTTTTCAATTTT	84708
rs561250620	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53619904	TTTTAATTATAACCA[A/T]CCCAGTGGGTGTGGC	84708
rs561267867	in-del	-/A/AAA	0.428128	0.197221	intron-variant	LNX1	GRCh38.p7	4:53583553	ACCCAAAAATACAGA[-/A/AAA]AAAAAAAAACCCTTT	84708
rs561271573	snp	A/G	3.30579e-05	0.00406544	synonymous-codon, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508146	AGCCGTGGCTGTGAG[A/G]CTCGCACAGCCGTCT	84708
rs561277036	in-del	-/CAAAAAA	0.00318978	0.0398085	intron-variant	LNX1	GRCh38.p7	4:53540680	AGCAAAGCTCTGTCT[-/CAAAAAA]CAAAAAACAAAAAAC	84708
rs561279000	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53536307	CCTACCTCGCAGTGC[A/G]AATGAACAGATTCTC	84708
rs561304582	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53501450	GTGCCACCATGTCCC[A/G]CTAATTTCATTTTTT	84708
rs561310007	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53625146	AAAACATAAGAGTAA[A/G]TCTTTGTGACCTTGG	84708
rs561313727	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53644124	AATGGAGGTCAGGAA[A/C]GGTGGCTCATGTCTG	84708
rs561320069	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53518438	CTATCGGTTTACAGA[A/G]TTAGTGTCTGTAAGA	84708
rs561331638	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53479619	GAGGAGGAGAGTTAC[A/G]TATGAAAGAGATGAC	84708
rs561336411	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53467792	GAGAAGTTTAGAGAA[A/G]AAAGAATAAAAAGAA	84708
rs561341069	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53539939	GGCATCCATGGCAAA[G/T]GTTGACTTGGCCATG	84708
rs561344713	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53549760	CATGGAGTTTTATTA[C/T]AATCTTTTCTCTCCT	84708
rs561360778	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53596581	ACAGGGTGGATTATT[A/C]CCAGGGAATTTTTTG	84708
rs561371924	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53641433	GTAACATTATCCAGG[C/T]AGTGCTGAAGAGGAA	84708
rs561373731	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53634533	ACAGGTGTGAGCCAC[C/T]GCCCCCAGGCTCAGC	84708
rs561386347	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53624253	CCAAATCTCACCTTG[A/C]ATTGCAGCTCCCATA	84708
rs561418086	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508624	ACCCTCACTCTTCTT[C/T]TGGATTTTGTTCCCA	84708
rs561428207	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53563719	TTTGAATTTTTGGTA[A/G]AGACGGGGTTTCACC	84708
rs561428980	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53505791	GCTTCAAAAACACCT[A/C]AAAAGGGGGCTGAGG	84708
rs561434283	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53502162	TTACTATATGCTGGC[A/T]TTGAGCTAAGCTACT	84708
rs561439970	snp	C/T	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53583413	GGAGGCAGGTGCTTA[C/T]AGGCTGCCGCCAAGG	84708
rs561458690	snp	C/T	0.00438332	0.0466095	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53603448	TGTCCACCATGGAGC[C/T]TGTGTTAGGCCGTTC	84708
rs561490348	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53512227	TGTCCCTGGAGAAAT[C/T]TGGAAGTTTTTCAAT	84708
rs561497304	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53497734	TAGCTGATTGTACTG[A/C]GGCCTGCCCCGAGGG	84708
rs561554745	snp	A/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53624498	ACATGCAACTGTGAG[A/T]CCATTAAACCTCTTT	84708
rs561567073	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53486396	AGCATCCCTCTCTTT[C/T]TTCTACAGGCCAAGA	84708
rs561569946	snp	A/C	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	LNX1, LOC101928879	GRCh38.p7	4:53576475	TCTTCCCAGGACAGC[A/C]CTGCCCTTCCCATGA	84708
rs561581344	snp	A/C	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53590075	ACAAGTGGTGGCCAA[A/C]CCCCCCCCCTTAAAC	84708
rs561602160	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53553143	CATTACTACAACCCG[A/C]GATCTCAGAACTCAC	84708
rs561604588	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53583848	GGTGCCATACTTGGG[G/T]TTGTTTGTAAAAACT	84708
rs561618799	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53593660	GCAGGGGTTAAAAAA[A/C]ATAATATGGGCTTTT	84708
rs561627568	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53607045	CCGTTTGAAAACCTG[C/T]ACAAGACAAGGATGC	84708
rs561644652	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53629765	CCAGCTGATGTCACC[C/T]GGAAAATGTGGAGGC	84708
rs561658252	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53600455	AACTTTTGCTTCCAA[A/G]AAAGGGCAGGCCCTC	84708
rs561679806	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53533461	TGGAGTGCAGCGGTG[C/T]GTTCTCAGCTCACCG	84708
rs561700408	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53535725	CCTTACATATGCCAT[A/G]TACTTCCTAGTCTAT	84708
rs561710303	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507720	TCTTGAGCAGCATGG[C/T]TGAAAAATTACTGAC	84708
rs561714100	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53627743	GATTTAACTAACACA[A/G]CACATTGAATCAGCA	84708
rs561738590	in-del	-/T	0.00279162	0.0372561	intron-variant	LNX1	GRCh38.p7	4:53477278	TAGTCTTGTTCACTA[-/T]TTAATCAAAGAAAAC	84708
rs561787078	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53628379	CAAATAGCCAAGAAA[C/T]ATGGAAAAATGTTCA	84708
rs561818803	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53553934	CCTGTATAGCAGACA[C/T]ACCTGCATGTGGTTC	84708
rs561845916	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53489124	AAGTGCCTGATATAT[C/T]ATTAAAAAGTTTATG	84708
rs561849683	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53614728	CTACGCTGTTTATGG[C/T]TCACGAGTTCATCTC	84708
rs561864873	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53585036	TGGTGGTAAAAGATC[C/T]ACCCAGGATGCCTTC	84708
rs561866121	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53504800	ACGGAGGCCCAAGAA[A/G]AGAGACATGGGGAAA	84708
rs561877672	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53582411	AGATCACAAAACGAC[C/T]GGATCCTGTAAGAGC	84708
rs561906898	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53622747	AGTTGCTTGTGTTTA[C/T]TGGGAAAACACTCAC	84708
rs561910092	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53607351	AAATTGAGAATGCAA[C/T]CTCATTCACGATGGT	84708
rs561944102	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53581156	GGTATACTGGTCACC[C/T]GGGACCATGACAGTT	84708
rs561945783	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53613726	ATGGGTATTTAGGTT[C/G]ATTCCATGTCTTTGC	84708
rs562011572	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53491602	TTGGGGACAAATGGC[A/C]CATGAAAGCAGATTT	84708
rs562021113	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53532510	TGGTGACACAAAACC[A/G]TCAGCTGCAAAATGT	84708
rs562068358	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53481980	ATGATTTCTAGTTTG[C/T]TGGGTTTTTTTGTTA	84708
rs562072271	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53524562	TCTAACACAACCAGT[A/G]AAATGACAGATCAAG	84708
rs562092501	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53613207	ACCCCCTACACATAA[A/C]TGTACACATGAACAT	84708
rs562094199	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53482720	GGGAGGGTGAGTGGG[G/T]TGAGGGATGAAAAAC	84708
rs562115676	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53633351	CAATAACTTTCTTAG[C/T]CTCTATTCTCTTTCT	84708
rs562136587	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53585933	AGGAATGGGGTGAAT[A/G]CTCCCAACGATCCTT	84708
rs562158030	snp	A/G			intron-variant, synonymous-codon	LNX1, LOC101928879	GRCh38.p7	4:53576057	GGACCAGCTCCAGGA[A/G]CTCTGCATCCCCCAA	84708
rs562163676	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53626051	TAACAGAATGTTATT[C/T]ACCAATAAAAAGGAA	84708
rs562187906	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53651674	ACCCTACACACCCGT[A/G]AGCAGGTCACAGCTT	84708
rs562226496	snp	A/C	0.00159617	0.0282053	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53518509	CAAATTAATAGTAAC[A/C]TAATTACAGCCAACA	84708
rs562230015	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53465252	TTCCTATCTTGCAGA[A/G]AAAATAAGGGTTTGG	84708
rs562247561	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53572413	ATTCACTGACATAAT[A/G]AGCGTGGAAAACATG	84708
rs562252330	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53559186	GCAATGAACTGCGTA[A/G]TCATTAGGAATTTGG	84708
rs562253330	snp	G/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53645105	AAAAGAACAGAAAGT[G/T]TGGCTTAACTCTATT	84708
rs562265059	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519285	GCACTCATATATTCA[C/T]ATTCATGGTCTAAAC	84708
rs562271531	snp	C/T			intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53574379	TGCCTAAAGTAACTC[C/T]AAAAAATGTAATTTG	84708
rs562279274	in-del	-/AAAC	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498466	GAGCAAGACAGAGAG[-/AAAC]AAAGATCTCAATTAA	84708
rs562290435	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53525238	ACACATCCCAGCACC[C/T]TGGGAGGGTGAGGAG	84708
rs562292929	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53470199	AACATATGCAAATCA[A/G]TAAACGTAATCCAGC	84708
rs562315312	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53564848	AAGCGCAAGGAGTCA[C/G]GGAGTTAGTTCCCTT	84708
rs562327413	snp	C/T	0.00636936	0.0560724	intron-variant	LNX1	GRCh38.p7	4:53564542	AGAATAATTATTCCC[C/T]AGAGATGTCCAGCTC	84708
rs562331667	in-del	-/T			intron-variant	LNX1	GRCh38.p7	4:53631862	GGTGGAGCCTGAGCC[-/T]TTTTTTTTTTAAGTC	84708
rs562381188	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53651314	CCTGCTCTGCACTGC[A/G]TCAGCATTCCTTGGG	84708
rs562381599	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53552551	TTAAATATTTAGGCT[A/G]GGCGCAGTGGCTCAC	84708
rs562405266	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53546638	ATAGGGGGATTAGAC[C/T]AAATCATCTCCAAGC	84708
rs562407290	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53470077	CCTGGATGAACACCA[A/G]TGCAAAAATCCTCAG	84708
rs562420641	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53592577	AAGATGGCCTGCCTG[C/T]CCAGAGAGAATTTTT	84708
rs562445686	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53467801	AGAGAAAAAAGAATA[A/G]AAAGAAATGAACAAA	84708
rs562451038	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53651260	ACTTTATGTTGAGCT[C/T]GTTTGAAGCTCACCT	84708
rs562492455	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53646637	TTTGAATTTTTATAT[G/T]AAATCTCCTGATTGT	84708
rs562501563	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53633513	GATCCTTGTTCCGTG[A/G]GCTATGGCCAGGGAA	84708
rs562515144	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53465143	TTTTCCTTGCAGGAA[A/G]TATTAAGCTCAGTAA	84708
rs562521962	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53618944	TTTTGTAGATACAGG[G/T]TCTTGCTATGTTACG	84708
rs562536721	snp	A/T	0.00438332	0.0466095	intron-variant	LNX1	GRCh38.p7	4:53469429	CATCACAATTAAAAG[A/T]ACTAGAGAAGCAAGA	84708
rs562564356	snp	C/T	0.00597247	0.0543191	intron-variant	LNX1	GRCh38.p7	4:53625236	GGTTTTCATCACAAT[C/T]AAATATTTTTGAGCC	84708
rs562580003	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53580378	CTGCAAGCTCCCCAA[G/T]TTATCAGTGTCTCTC	84708
rs562586449	snp	A/T	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53464639	GTATAGCAATGTTTA[A/T]TATAAGTGAGGTTGC	84708
rs562587669	snp	A/G	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53558928	TGAGACTGCATCACC[A/G]GCCTCAACACTAAGA	84708
rs562590701	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53504121	ACCTGGGCTACAGAG[A/C]GAGCGAGACTCCGTC	84708
rs562616365	snp	A/C	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	LNX1	GRCh38.p7	4:53558041	CAGCCAAGCTCCTTT[A/C]AGCAAACCTTGCCAT	84708
rs562617684	snp	A/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53586830	AAATAAAAAATAATG[A/T]TTATTACTATTTAAT	84708
rs562637119	in-del	-/TCACACAG	0.00199481	0.0315187	intron-variant, utr-variant-3-prime	LNX1, LOC101928879	GRCh38.p7	4:53577255	TAGGGGAAAAATGGT[-/TCACACAG]GATGAACTAAAGCTC	84708
rs562643740	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53503055	CCTGCCTCAGCCTCC[C/T]GGAATTTGGTCATAT	84708
rs562651164	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53511058	TAAGGTAGGTAAGTA[A/G]CCTTTCCTTTGGTCT	84708
rs562707931	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53491098	AATGCCATATGTAGT[C/T]AAGATTTTTCCAAAT	84708
rs562727845	snp	C/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53538375	CTGCTACCTAGAACA[C/G]CTTTCCCTGTGAAGT	84708
rs562727906	snp	A/G			nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53604825	GAAGACAGGTCACAG[A/G]CCACCTTTCTCAAGA	84708
rs562738931	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53643999	TAGTCTACAAAATTA[C/T]TTACTCTAAAAGTCT	84708
rs562746208	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53626760	TTGTGATCCAAGGAA[A/G]GCTCCAGGGTTTCTT	84708
rs562757908	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53524352	TGGCACTTAAGGTAA[C/T]AAATGTTTGTTGAGA	84708
rs562761898	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53632773	GGAAGAGGAAAAGAG[C/G]CCTCTATGGACAACA	84708
rs562763088	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53626994	TTATAAAGATTGGCC[A/G]GGGATCCCAGTTTGG	84708
rs562763104	snp	A/G	0.00199481	0.0315187	nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53603824	CAACATGAGATTTGG[A/G]TGGGGACAAATATCC	84708
rs562766471	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53490128	CTCATTTAAATATTG[A/T]TTCATATAAGGAAAA	84708
rs562777118	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53579832	ATACTCCACTAGAAG[G/T]ACAATTGGATAAATA	84708
rs562782443	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53496941	AGTGTGTGAGCACGA[C/T]GGAGTGTATGTGCGT	84708
rs562783862	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460247	TACTAACGATTGTGG[A/G]AAAAAAGAGCTTTAG	84708
rs562813619	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53505671	ACATTTAGTGGACAC[G/T]TATGTGCCAGACACT	84708
rs562833690	snp	A/C	0.000399281	0.0141238	intron-variant, downstream-variant-500B	LNX1, LOC101928879	GRCh38.p7	4:53577648	TTGAACTCCTGGCCT[A/C]AAGCAATCCTCCCAT	84708
rs562885839	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53619699	TTTTCACAAGAACCA[A/G]TGTTTTCAATTCTAC	84708
rs562891321	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53530928	CAGCACCCTGGGAGG[C/T]TTAGGCAGGAGGTAT	84708
rs562901842	snp	C/T	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53537629	AACACAGGGCTCTCC[C/T]GCCAGGCTTGTGAGA	84708
rs562920900	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53615522	TCTAGCCAATCGCCA[C/G]AGCCAACTCCCAGAC	84708
rs562928494	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53488341	TTTCCCTGTGACAAT[C/T]CTATTTGAGGATCAC	84708
rs562933022	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53544486	GATGTGAGCCACCAT[A/G]TCCGGCCTGAGAGGT	84708
rs562958155	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53622926	TAAAATATTATTCTT[A/C]TGGAGGAGAGTTTTA	84708
rs562980404	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53493084	AAGCAGTTCTCCTAC[C/T]TCAGCCTCCCAAGTA	84708
rs562993817	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53481427	CCTCAAACAAGATGA[C/T]TCTTGGTAAAAACAT	84708
rs563014901	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53526301	TGATGTAAAATGATG[A/G]GTACTGGTTATTAGT	84708
rs563053408	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53469081	CCATAACTGACCACA[C/T]AGTTGGAAGTAAAGC	84708
rs563066417	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53605903	GAATGCAGCAATCAC[C/T]AGATATCAGCTGGTG	84708
rs563095620	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53521559	ACCAAATATTTTTAC[A/G]TGAAACAAAAATCCT	84708
rs563101141	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53563785	TGATCCACCCGCCTC[A/G]GCCTCCCAAAGTGCT	84708
rs563119666	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53474344	CCAACACCTGGTTTT[A/G]TAAGTAAAATTTTAT	84708
rs563131054	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53527714	AAGCTCATACTCACA[C/T]ATCCAAATTACAGGG	84708
rs563138574	in-del	-/A/AAAAAAA	0.499035	0.0219437	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53506856	AGCAAAACTCTGTCT[-/A/AAAAAAA]AAAAAAAAAAAAAAA	84708
rs563142916	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53650721	TCCGTGTCCCCCCAA[A/G]AACCTCAACCCTAAC	84708
rs563175316	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53571301	TGGGATTACAGGTGT[A/G]AGCCTCCATGCCCCG	84708
rs563196343	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53494196	ACCATTCTTGTGGTA[C/G]TAAGTCTCACAAGAT	84708
rs563198537	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53629232	TGATTAGGGGGCTAC[C/T]GAAATAGAGGGGTGG	84708
rs563208257	snp	A/G			intron-variant, nc-transcript-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53523274	ATTTAAAGCTGTACA[A/G]TTTTTTTTGTTTGTT	84708
rs563215861	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53581758	TGGGGATTATGGAAG[C/G]TACAATACAAGATGA	84708
rs563232419	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53530082	TTTCTCCATCAAAAA[G/T]TGTTCTAAAGCTATT	84708
rs563271059	in-del	-/TG			intron-variant	LNX1	GRCh38.p7	4:53464926	TTCATGAATTTCTTC[-/TG]TGTTTTTTCTGAAAA	84708
rs563273693	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53520640	TTGGTTAACTTTTGG[C/T]CCCTGCAATTCTTGG	84708
rs563283455	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53616287	CATAGACACAAATAA[C/T]TCCTATATACCATAC	84708
rs563298409	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53637761	TTAAAATGTAAAAGA[A/C]GGAGTGTCTTAGAAT	84708
rs563311511	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53465948	GTATAGAGTTTGTGC[A/G]TAGTATATTGGCATC	84708
rs563322055	snp	A/G	0.00318978	0.0398085	intron-variant	LNX1	GRCh38.p7	4:53471894	ACTGTTGGTGGGACT[A/G]TAAACTAGTTCAACC	84708
rs563323571	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53470795	AAGGGACGTGAAGGA[A/C]CTCTTCAAGGAGAAC	84708
rs563324128	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53555290	CTTTGGTGACAACCA[A/C]AGCCAGCCCCTAACC	84708
rs563338704	snp	C/T	0.00318978	0.0398085	intron-variant	LNX1	GRCh38.p7	4:53609785	ATTATATATAATATA[C/T]TATTTAAATATAAAA	84708
rs563366964	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53565639	AGCAACAGAACAAAG[C/G]TGGACAGAGAATGAC	84708
rs563408792	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53499347	CATTTTTTGTGGAGA[C/T]GGAGTTTTGTCATGT	84708
rs563415234	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	LNX1	GRCh38.p7	4:53653799	TCTGACTCTTTTTGG[C/T]TCTACCCCTAATCTT	84708
rs563418845	snp	A/T	0.00119737	0.0244387	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519877	CCAACCATCTCAGAT[A/T]GCCCAGGACTGACTG	84708
rs563428803	snp	C/T	1.71366e-05	0.00292712	synonymous-codon, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573955	GTGGGCTTGGCCACA[C/T]ACTGCACACAGGGGT	84708
rs563442661	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53573333	GTGATAGTTGCACAA[C/T]ACATGAAAGTACTTA	84708
rs563454753	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53467522	TTGAGAGAGGAAGGC[A/T]TCAGAAGATCACACT	84708
rs563458814	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53561637	ACAGACGATCCAGGT[C/T]AGACCTTTGGAGAAG	84708
rs563460774	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53483519	TATGAAACTCACATA[A/G]ATAGAGCTCTCTGGT	84708
rs563472297	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53533689	ACAGGCATGAAACAC[G/T]GTACCCAGCCTGGAG	84708
rs563491110	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53595024	CTTTTCTATCTCTAG[C/T]TGGACAGTAAGTGAG	84708
rs563515326	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53641639	CATCACTGCAATCAA[A/G]GAACAAATTCATTTT	84708
rs563524124	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53569670	TGAGAAATGGGATCT[A/C]ATTAAACTAAAGAGC	84708
rs563524269	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53561345	CGATTCTCCTGCCTC[A/G]GCCTCCCGAGTAGCT	84708
rs563536434	snp	A/G	0.0271762	0.113356	intron-variant	LNX1	GRCh38.p7	4:53568402	GACAAAAACCACATG[A/G]TTATCTCAATAGATG	84708
rs563542894	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53471552	CATCAGAGTGAACAG[C/G]CAACCTACAGAATGG	84708
rs563545889	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53466792	GGGGGAGGGGCGCCC[G/T]CCATTGCCCAGGCTT	84708
rs563590335	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53475814	ACAAGTAATTACGTC[A/G]CTGTAAGGCTCTAAA	84708
rs563597788	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53567875	ACAAACACCTCTATG[C/G]AAATAAACTAGAAAA	84708
rs563627640	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519865	CATATAGGGTGACCA[A/G]CCATCTCAGATTGCC	84708
rs563660917	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53526205	CCCCATCACTGGACA[C/T]GGCACACTGCTCCCT	84708
rs563681904	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53537915	CAGTGACCTGAGTGA[A/G]TTGCATCTGTACCTC	84708
rs563688660	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519627	TCTGTCTGAGATCTT[G/T]TTGATTTAAGCCCTG	84708
rs563701893	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53607579	TCCTATCAAACTACT[A/T]ATGACATTCTTCACA	84708
rs563704578	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53605937	CCGTTTCCCAGAAGA[A/G]GGATTGCTGGGTCAT	84708
rs563715440	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53475185	GCACCTCACATTGTC[A/C]TCTCTTACACAAATG	84708
rs563719704	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53622299	AGTGATTAAGTTCTT[C/T]AGAAAACCTATTGAC	84708
rs563730933	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53636155	AATCAAAGAGGGATC[C/T]CAGAGACTGCACATC	84708
rs563744627	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53476642	CACAACCAAGACTGG[G/T]TCTAATTAAGATGCT	84708
rs563781715	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53651888	GTGAAAGTAAAGAAG[C/T]TTTTAATGAAGGCCA	84708
rs563789798	snp	C/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53603246	GAGCCGACTCCTCAC[C/T]GCATGTGAGGACCTA	84708
rs563811795	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53613819	ATTCCTTTGGGTATA[C/T]ACCCAGTAATGGGAT	84708
rs563813691	snp	A/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53622070	TAATAAGCAATTTTC[A/T]TGACATTTTTTATAG	84708
rs563814296	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53506648	TCACCTGAGTTCAGG[A/G]GTTCGAGACTAGCAT	84708
rs563827621	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498432	TTATATACAGAGAGA[A/T]AGGGGGGAGAGAGTG	84708
rs563831212	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53533977	ACACATCAAGGTGCC[A/T]GGGCAGTGAGGGTGG	84708
rs563840093	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53506566	TGTAAAACAGGAATA[G/T]GAGTGGCGCCAGGTG	84708
rs563841665	in-del	-/A			intron-variant	LNX1	GRCh38.p7	4:53541478	GCACATTTCATATAT[-/A]TTTTTTTTCTAAAAG	84708
rs563856991	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53601309	CAGGGTGGCCAGACT[A/G]GTCCTTCCAGTTGTG	84708
rs563870301	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53568580	CATTCCCTTTGAAAA[C/T]GGGCACAAGACAGGG	84708
rs563879514	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507250	AAGGTGATCAGATTG[C/T]GTCATCCCTGAAGTC	84708
rs563912850	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53547500	AGCATGTGCCTTGAA[G/T]CACTAGGTCATCTCA	84708
rs563929657	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53540498	TTAGCCTGGCTGACA[C/T]GGTGAAACCCCGTCT	84708
rs563943220	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53635265	GTGCAGAGGCCAGAT[A/G]TGGAGAGAGAAGGAA	84708
rs563952081	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53491787	TAAGTGCTGAGGATA[C/T]GATACTTTTTTTTGT	84708
rs563963580	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53527656	CATTGTCACCTTTGC[C/T]CAGCAAAAGCCTGAA	84708
rs563982231	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53647048	GGTTCTCCATGCTCC[A/G]TTTTTTCTCTTTTTC	84708
rs563989896	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	LNX1	GRCh38.p7	4:53653096	GCTTACCGTCTACCA[C/G]GTTCTGTAGTAATTA	84708
rs563996221	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53622787	GATGAGAATAAGAGA[A/G]GGAGGCTGACCCATG	84708
rs563998608	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53589920	CAGTGATGAAATTAT[G/T]TATTTAATCATAAAT	84708
rs564000103	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53601974	CCTCACCCCTGCTCA[C/T]GTGACTGACTTCTCC	84708
rs564017459	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53513154	TGTTCCCATCGCTTC[C/T]AGGCCTTCCCTGATC	84708
rs564025771	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53587580	ACACTTTAGAGCATC[A/T]CTTATGTGTCCTCGC	84708
rs564062624	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53551604	GAATGCCACTGTGGA[C/T]GCGGACAGCCCACTC	84708
rs564114824	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53475639	GATGCTAATATTTAG[C/T]ATTATTCACACATTG	84708
rs564155126	snp	A/G	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53567832	ACCACCGATCCCACA[A/G]AAATACAAACTACCA	84708
rs564184474	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53573270	TCGTGTTTAATGGAT[A/G]TAGAGTTTCCATTAT	84708
rs564221996	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53526635	GTAATCTAGTATCTG[C/T]TTGAAATTCTCTTTT	84708
rs564242837	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53484034	GGGCTGGAGGAATCT[C/T]GTTTGCCCCTCTACC	84708
rs564249944	snp	C/T	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53471164	ACCAATGGAACAGAA[C/T]GGAGCCCTCAGAAAT	84708
rs564287638	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53616165	TGTTTGCGTTTCTGT[G/T]GGCTTGGATATTTTA	84708
rs564305498	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53505861	TCTGGAAGAAGGAAC[A/G]TGAATGCCAGCTGAA	84708
rs564309534	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53601106	AAGGGAGGGAGGGAG[C/G]GGGGGAGGGAAGGAA	84708
rs564312865	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53477399	TAGGCCTCCAGTAAA[C/T]ATGGATTGAATGAAA	84708
rs564325658	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53607385	GAAAAGATAAAATAC[C/T]TAGGAATATAGCTAA	84708
rs564327612	snp	A/G	4.94214e-05	0.00497074	synonymous-codon	LNX1	GRCh38.p7	4:53476839	CAGGGCTGCTGGGCT[A/G]CTGCAGTCTTCCTGG	84708
rs564348235	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53600593	CTCTCAGTCAGATTC[C/T]GACTAACAGGGTCTC	84708
rs564356269	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53574940	TATAAGGGGCCTTTA[A/G]GCTTTGTTCTAATAG	84708
rs564406552	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53478508	TCACCTAACAAGCTA[C/T]TAATTTCTCTTGATT	84708
rs564432926	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53526081	AAAGGAAAAGCATTA[C/G]AGTATGTTTTGGGCA	84708
rs564437061	snp	A/G	0	0	intron-variant	LNX1	GRCh38.p7	4:53490005	TTTTTTGCAGGTATG[A/G]CAATGCAAATAGTCC	84708
rs564440499	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53534860	TGGGGACCTTGGCAT[C/T]CTTGCCCATAGTAAT	84708
rs564441200	snp	C/T	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53651112	AGAATCAAGAACAGA[C/T]AGTCTAATTCCTCAG	84708
rs564466822	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53518736	CAGAGAGAACTTTAA[C/T]TGAAGTGTGCACCTC	84708
rs564494830	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53533250	CAAATGAAGAGAGGT[C/T]CAATAGAACATACAA	84708
rs564497103	snp	A/G	0.00318978	0.0398085	intron-variant	LNX1	GRCh38.p7	4:53525331	TACTGAAAATACAGA[A/G]GTTAGCTGAGTGTGG	84708
rs564518362	snp	A/T	0.00478085	0.0486577	intron-variant	LNX1	GRCh38.p7	4:53467925	ACACTCTGCAAGATA[A/T]TATCCAGGAGAACTT	84708
rs564519723	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53641483	CAGCCAAAGACGAGA[A/G]AAATGGACAAAATAC	84708
rs564527176	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53627450	AATAACTTGGGTTGA[C/T]TCTCACATTATTTCA	84708
rs564533881	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53564545	ATAATTATTCCCCAG[A/C]GATGTCCAGCTCCTA	84708
rs564562449	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53629471	AATGTCCCAGGCCCT[A/G]CCAAAGCTTGGGTTC	84708
rs564565761	snp	A/G	0.0267878	0.112589	intron-variant	LNX1	GRCh38.p7	4:53570289	ACAATGATAGACTGG[A/G]TTAAGAAAATGTGGC	84708
rs564573088	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53465848	TCTAAGCAAATTTTA[A/G]TTTTCACAAATACCT	84708
rs564579580	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53559327	ATAATTCATGATTTT[A/G]TTGAGGTCCAAATTG	84708
rs564579929	snp	G/T	0.0107246	0.0724382	intron-variant	LNX1	GRCh38.p7	4:53472152	CCATGGAATACTATG[G/T]AGCCATAAAAAAGGA	84708
rs564583713	in-del	-/T			upstream-variant-2KB	LNX1	GRCh38.p7	4:53654077	TTGAGGTTGGTCAGC[-/T]TTTTGTTCTTAACAG	84708
rs564602661	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53512335	AAACACATCTGCAAG[C/G]CAGCTCTAGCTCCAG	84708
rs564612375	snp	A/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53594106	ATTTGGAAATTAATT[A/G]GTAATCTGGTCTATA	84708
rs564612698	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53619042	AGGTGTGAGCCACTG[A/C]ACTCGACCTCACTTT	84708
rs564622709	snp	A/G	0.000399281	0.0141238	intron-variant, synonymous-codon	LNX1, LOC101928879	GRCh38.p7	4:53576312	CAAGTTCCAGGAGCT[A/G]CGGTACAGCGTGGCC	84708
rs564627004	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53569978	GATACTATCTCACAC[C/T]AGTTAGAATGGCGAT	84708
rs564650624	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53553644	TTCAAAAAGAATGTT[C/T]ATGGAGGTCTGCGGA	84708
rs564661925	snp	C/T	0.00119737	0.0244387	intron-variant, synonymous-codon	LNX1, LOC101928879	GRCh38.p7	4:53575838	CCAGCTACTAGGGGA[C/T]CTAAACAGGAGCATG	84708
rs564667032	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53513128	TTTAACTCAAAAACC[A/G]CCCAGGGAAATGTTC	84708
rs564675686	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519411	ACAGTAACCACCTGA[A/G]CTATCATTTGTTCAG	84708
rs564677190	snp	G/T	0.0154538	0.0865337	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53593681	ATGGGCTTTTTTTTT[G/T]GGCCATTAGGGCTGT	84708
rs564690377	snp	A/G	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53466408	AGTCTACAGCTCCCA[A/G]CGTGAGTGATGCAGA	84708
rs564711269	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53502400	ACTGTACTCTAGTCT[A/G]TCAAGTGTACAATAG	84708
rs564726807	in-del	-/AGAT			intron-variant	LNX1	GRCh38.p7	4:53652033	GTGAGAGAGAGAGAG[-/AGAT]AGAGAGAGAGAGAGA	84708
rs564734900	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53640969	TGGCCGGGGCTGAGG[C/T]CTGGCCGTTGTTTGG	84708
rs564740304	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53646525	CAGAACAGTGCCTGG[A/C]ACAGAATTGTCACCC	84708
rs564756282	snp	C/G	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53592241	ATTCAGATTGGAATG[C/G]TAGTACTGTCATTAG	84708
rs564770490	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53479453	AATGGCTGAAATACC[A/G]CAAATATGGCATGTG	84708
rs564804560	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53468265	TAAGTGAAGGAGAAA[G/T]AAAATACTTTACAGA	84708
rs564827847	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53597407	ATGCCACCACCTGCC[A/T]GCCCCCATGCCATAG	84708
rs564856505	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53614419	CCTTTGGGATCTCTA[C/T]CTCTATCCCTTCTCA	84708
rs564864497	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53611251	AATAGTGAAAAACCA[A/G]CCTCTATGAAATACT	84708
rs564875472	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53616270	GATAGACACCTTCCC[C/T]ACATAGACACAAATA	84708
rs564879172	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53617750	TTGTAATACAGAGAT[A/G]TTATTGACTAAACCT	84708
rs564890164	snp	C/T	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53463395	CTTTTAGTGGTGTTT[C/T]GAGTATTTAACTTTA	84708
rs564920130	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53557848	AGGCACATAAACACA[A/C]AGGCACGGACAGAGA	84708
rs564932618	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53643176	TCTTTTTTAAGACAG[A/G]ATCTTGCTCTGTTGC	84708
rs564970014	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53638276	AAGAAATAGACCTTT[C/T]GATACTTTAATAATG	84708
rs564974580	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53557271	TCCAGACCATTGCAG[C/G]AAGAAATATATGAAG	84708
rs564998216	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53529388	GAGAACTAGAGGCCA[C/T]TGCAACAGAAAAACT	84708
rs564999001	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53465690	AAATTCTGATACATG[C/T]TTAAATTGTACATAC	84708
rs565009527	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53486372	GGCTACAGGCATGCC[A/C]CTTCACCCAGCATCC	84708
rs565016579	snp	A/G	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53624485	GTCCTCCCCAGCCAC[A/G]TGCAACTGTGAGTCC	84708
rs565039714	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53488091	TCAGACATCATCTCA[A/T]CCAACATTTTCTCTA	84708
rs565047762	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53554036	GCCCCTAGCCTGTCC[C/G]AGGAAACGTGGGCTG	84708
rs565060672	snp	C/T			utr-variant-5-prime, upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53591570	AAATGGGTGACATCA[C/T]GGAAGCCCCGACAGA	84708
rs565084795	snp	G/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53638865	GTTGCAGAGAAAAGG[G/T]GACACTTATACACTA	84708
rs565107915	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53644653	TATTCCAGGAGGGAG[C/T]GGGATTCCATGTCAG	84708
rs565112865	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53473423	CCATCAATGGTAGAC[C/T]AGATAAAGAAAATGT	84708
rs565113492	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53550388	TTCCTTCCAGGTCCT[C/T]GTCCAAATTCTACTT	84708
rs565131656	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53640959	CCTCAATCCCTGGCC[A/G]GGGCTGAGGCCTGGC	84708
rs565133900	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53462515	ATGGCTATTTTGTTT[A/G]TATACCGTACCTTAA	84708
rs565164984	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53486279	ACTTAGTGAAGCCAC[C/G]CAATCGGCAGAGCGC	84708
rs565167378	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53642634	TTTTCTGGGTGTACA[A/C]AGATTTTCTGCCAGA	84708
rs565172143	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53509534	TCTAGGGAAATTTTA[C/T]TTACCTGGCTAAACT	84708
rs565185304	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53649983	CAGAGAAGAAAAAGG[A/C]GCAGGGACTGCCCAA	84708
rs565191277	snp	G/T			intron-variant, nc-transcript-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53523191	CCAACCTAGGCATGG[G/T]TTTATGTTCCTGACA	84708
rs565200527	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53467025	AGCAGCTTGAGATCT[C/G]AGAACGGGCAGACTG	84708
rs565204113	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53557672	TTATTGAGAAAGTAC[C/T]GCATCTGTTAATATG	84708
rs565205219	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53549698	GTTAAAGGAGATATC[A/G]ATAAGATGGCCTTGA	84708
rs565244476	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460519	AGCAATGCATTTTAA[A/G]AAATATTTTAGCTGT	84708
rs565251527	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53560800	AGACTTTGTATTACA[A/T]GAGAAAAACAAAACT	84708
rs565273838	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53513997	CTACTTCTTCAGGGC[C/G]TCTGCACTTTGCTGC	84708
rs565283126	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53467437	AAATCAGAGCGCCTC[C/T]CCTCCTCCAAAGGAA	84708
rs565287703	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53602716	ATATTGTTTCAAGGA[A/C]TGAAAAACACGTGTT	84708
rs565309188	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53530248	TATACAGAAAGAATC[G/T]TAAGTAAAAAAGCCT	84708
rs565334020	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53561313	ACTCATTGCAACCTC[C/T]GCCTCCCAGGTTCAA	84708
rs565338292	snp	C/G/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53646273	GTATTGGTAAATGAC[C/G/T]GGAGTGGAGTAATAG	84708
rs565340066	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53465459	TTTGGCTGACATCAC[A/G]GCAAAATTTTCTGAA	84708
rs565344661	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53471524	AGAGCTTCTGCACAG[C/T]GAAAGAAACTACCAT	84708
rs565356570	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53514614	GGGTCCCTCCCACAA[C/T]ATGTGGGAATTAGGG	84708
rs565359614	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53546356	CAGACTCCATCAGAG[A/G]ATGCTGCATTCATGA	84708
rs565388836	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53477704	ATTTTCTATTTTTTT[A/G]TCTTCATCCTGTTTT	84708
rs565395453	snp	C/G	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53568255	ATCCTCAATAAAATA[C/G]TGGCAAACCAAATCC	84708
rs565420567	snp	C/T			upstream-variant-2KB	LNX1	GRCh38.p7	4:53653038	GCATCACCATCATCA[C/T]CATCGTCAGTGGCTG	84708
rs565423683	snp	A/T	0.00398564	0.0444627	intron-variant	LNX1	GRCh38.p7	4:53609736	TACAATATATAATAT[A/T]CTATTATATATTATA	84708
rs565425079	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53602115	GACAGAGTGAGAAAT[A/C]GAAACTAGGATCTGT	84708
rs565439056	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53582454	GTACATAAGCGAGCC[C/T]AGTCAAGTAATAAAG	84708
rs565453031	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53477091	GGGATGCAGAGAGGG[A/C]AAAGGTTTTCTTTGT	84708
rs565470071	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53522926	GACACATATACTTCT[A/G]TATGTTTATGATTTT	84708
rs565470087	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53493540	GGTCCTCTTCCACGA[A/G]GAGGGATAAGCTACT	84708
rs565476385	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53542832	GAGTGATGTTTAACC[C/T]GGTAAGAACCCCCCT	84708
rs565499529	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53630574	CCTGGTGTTCCTAAG[C/T]GCAAGAAGGCTGTGA	84708
rs565507667	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53521344	TCATTCCCAGACATT[C/T]GAAAACATTTCCTCC	84708
rs565566488	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53501173	AAGGACTAAAGGATA[C/T]AATCTTATTAGCTGA	84708
rs565589626	snp	A/G	0.00716266	0.059414	intron-variant	LNX1	GRCh38.p7	4:53470997	AAAAACTACTTTAAA[A/G]TTCATATGGAACCAA	84708
rs565614013	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53596518	AGACCTATATCTTAT[A/G]ACAATTACACATATT	84708
rs565618998	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508289	GCCATTCCTCAGTCA[A/G]CCCTCTTCAAATACA	84708
rs565624347	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53626303	GTCATAAAAATGTTC[A/T]GAAATTTAATGGTGG	84708
rs565624709	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53514332	GGTTGTATTAGTCCA[C/T]TTTTACACTGCCAAT	84708
rs565632401	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	LNX1	GRCh38.p7	4:53653854	TCTCTTGTGTCATGG[A/C]GGTTACCCAGGGCAG	84708
rs565643576	snp	A/G	0.0217236	0.101931	intron-variant	LNX1	GRCh38.p7	4:53566676	ATGTAAATGGACTAA[A/G]TGCTCCAACTAAAAG	84708
rs565650067	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53463421	CTTTATTGCCGCAGC[A/G]AGAACTCCGTATGTT	84708
rs565676560	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507680	CTTTTTTGTTTCTGG[C/G]CTGAACTGAATACAA	84708
rs565705286	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53587254	ACAGAAAGTTTACGG[C/G]AGACAACAAACGTTT	84708
rs565707777	snp	C/G	0.00438332	0.0466095	intron-variant	LNX1	GRCh38.p7	4:53471283	TGGGAAAACTGGCTA[C/G]CCATACGTAGAGAGC	84708
rs565726219	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53615670	TTGAGTTTTGAAGTG[A/G]TTGGTAATACAACCA	84708
rs565742301	in-del	-/A	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53606199	GGTAGACTAATAAAG[-/A]AAAAAAAGGGAGAAG	84708
rs565761531	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53567917	TGGATAAATTCCTTG[A/C]CACATACACTCTCCC	84708
rs565766337	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53512254	CAATGTAAAATCTCT[C/T]GATTTTTTAGATGGT	84708
rs565778221	snp	C/T			intron-variant, nc-transcript-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53500452	TTAAGAGTCTCCTTT[C/T]GTTATGGCATCTGGA	84708
rs565789804	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53548885	CACAGGAACATGGAC[A/G]GAGCTGGAGGCTACT	84708
rs565799757	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53628068	CTCTTCAAATTTTCA[A/G]GTGGGAGTGAAAATT	84708
rs565812326	snp	A/C	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53499696	TCAGATAATTTTGAA[A/C]ATTTCTTCCTTAAAG	84708
rs565837564	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53589247	AAAGGAAGAAATCAC[A/T]GCCAGCCAGCAACTC	84708
rs565881597	snp	A/C	3.44276e-05	0.00414881	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461056	ATCTAAAAAAAAAAA[A/C]AAAACAAGATATGAT	84708
rs565931277	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53534305	TTTCTGGGTAGGGGC[C/T]CATCTTCAACCCTGA	84708
rs565939378	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53555388	TAAGCACTTCAAGAT[C/T]CAGCTTAAACCCCCA	84708
rs565943402	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53642802	GAATGGTGCCATGAC[C/T]ATGAGAGGGGTCGCT	84708
rs565948240	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53593906	AGCTCATCGGCAAGC[C/G]GCAGAGCAGTTTTTA	84708
rs565960837	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53484193	AAGCCACCTAGGATA[A/G]TGTATTTTGTTATAG	84708
rs565966419	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460048	ATCTGGGTGGCCTCT[A/G]TGAAATAAATTAATT	84708
rs565974684	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53633393	TATATCTTCCTCATA[C/T]TATTGCTTCTTCCCA	84708
rs565980613	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53648907	CTATTGCCCTGAAAC[C/T]CACTGAGTGTGTATA	84708
rs565996469	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53554873	AAAAAAAAAATCCTG[C/T]CTTGCCCCTGCAGGC	84708
rs565999487	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53553325	CAAGAATGAAAATGG[G/T]GTGGCCTCATGAGAA	84708
rs566000383	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53561393	CCACCACACCCAGCT[A/C]ATTTTTCTATTTTTA	84708
rs566012190	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53529618	GAGACCCTGGGAACA[C/G]AGCAAGCACGGCATC	84708
rs566057278	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53646662	GATTGTTAGATGTTT[A/G]GTAGCTAATATAAAA	84708
rs566064898	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53540155	GAGAGTCTGAGGCTG[A/G]CAGATTGCTTGAGCT	84708
rs566065919	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53587758	AGCCAAGGTCTTGGA[G/T]ACAAGGAGACAGTGA	84708
rs566090024	snp	G/T	0.00398564	0.0444627	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53600711	TGGACGGCCTCTGTT[G/T]TTTTATTTTTATTTT	84708
rs566104541	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53584183	TTTTAAAACAGATAA[C/T]CAAGTTTTACAGAGG	84708
rs566139333	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53614968	CTTTTGGAGCTATTC[C/T]GAAATTTGTTCATCT	84708
rs566145844	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53647317	ATTAAGCATAATGCA[C/G]AGTGTCTCTTTTATT	84708
rs566161591	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53524393	CATTTCACACATAGC[A/G]TCTATCACTTTTAAT	84708
rs566166916	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53505723	GATTCAGAAAAATAA[C/T]CCCTGCACTTTGAGG	84708
rs566171619	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53551194	GCCCATAACTCTTAC[C/T]GCTTTTGGCAGTTTC	84708
rs566181260	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53534084	TAAGACTTGTGGAAG[A/G]CTTTCATAATAGGAC	84708
rs566185689	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53550569	GAACTTTGAAAGTGT[C/T]GGGAATGGCTAACAC	84708
rs566215091	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53556972	CTTGCTATTTTTCCC[G/T]TCTGGTTAGGTTCAT	84708
rs566258355	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53618067	ATAATCAAAAGATAC[G/T]GTGATTTTTAAAAGT	84708
rs566271253	snp	A/G			intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53559602	GTGAAATGAGGCAAT[A/G]CCCATAAACAACAAA	84708
rs566276622	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53535081	GAATCCTCCTTGCTA[A/T]AAGGAAAGAGAGGAG	84708
rs566289147	snp	A/G	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53534549	CAGAAGGCTGAGGTG[A/G]GAGGATCACTTAAAC	84708
rs566294712	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53542236	GTTTCCAGAAAACCA[A/G]GGATAAATAAACAAA	84708
rs566317706	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53633826	CAGCCACAAACCAGC[C/T]GTGGGACTTTGGGGA	84708
rs566318863	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS2	GRCh38.p7	4:53591214	AGTTTATTGTGCAAC[G/T]AGAATGTCAAAGTCA	84708
rs566336855	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53540722	AACCCCCCTGTTATT[A/T]TTATAAACAGAGCTA	84708
rs566337701	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53542911	CTGATGGTCATGAGC[C/T]CACCCAGGTGCCAGC	84708
rs566339713	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53496652	CAAGCCCACATATTT[A/G]TTCCCAGAATCCTAG	84708
rs566344076	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53628805	CAGCCATAAAAAGAA[A/G]TGAAATAATGTCTTT	84708
rs566351873	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53598407	CCAGCAAATTTTTGT[A/G]TTTTTTGTAGAGATG	84708
rs566359743	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53481018	GACTAAACAAGGTTT[C/G]TGTTGCTTAAACACG	84708
rs566375607	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53477742	CCCCTTTTGCTTAAC[C/T]TTCTTATACAGAATA	84708
rs566379185	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53635523	ATTTGGTATTAATAT[A/G]TTGCAATTATTTTAA	84708
rs566419071	snp	A/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53514754	CTGCCCAGGGAAAGT[A/T]CCCCCCTTGGACTAT	84708
rs566431677	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	LNX1, FIP1L1	GRCh38.p7	4:53462908	GTGGTGTGTCACATA[A/G]CACACTTTACATAAC	84708
rs566455165	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53471030	AAGAGCCCGCATTGC[C/G]AAGTCAATCCTAAGC	84708
rs566465945	snp	C/T	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53584836	GGTCAGTTTTTCAAA[C/T]AGCTAGTGCTTCCCA	84708
rs566539000	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53528990	AATAGCCCAATACAG[A/G]GAGAATGCATATTGA	84708
rs566568965	snp	C/G/T			intron-variant	LNX1	GRCh38.p7	4:53537510	TTTTATAGCAATACA[C/G/T]AGTGAGTAGTTTCAA	84708
rs566570194	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53644283	GCATGCTCCTGTAGC[C/G]CTAGCTACTTGGGAG	84708
rs566599878	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53535870	TGTATGTCTACATTT[A/G]ATATGACCCCTGATA	84708
rs566611267	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53510046	GAATCACAATTCTGT[A/G]TTTTCTTGCAAAGGG	84708
rs566625275	snp	A/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53596206	GATAGAATGCCATCT[A/G]GTTCTGTGTATATGG	84708
rs566625738	snp	G/T	0	0	intron-variant	LNX1	GRCh38.p7	4:53571401	AGTTCTTATAGGAGG[G/T]AGGCAGGAGTCTCAG	84708
rs566630627	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53630238	TACTCAGAATTGGGT[A/T]TTTATACAGTCGAGC	84708
rs566639560	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53612414	ATATAAAGATTCATA[C/T]ACAAGGTGTTTTAGC	84708
rs566647439	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53488509	GCAGAATAGAACCCA[A/G]AAGATGAGTTCTGGA	84708
rs566672169	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53532022	AGCTGTAAGAAATAT[A/C]CAAGACAAAAGCTGA	84708
rs566703742	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53626124	ATTATGCTAAGTGAA[A/G]GAAGTCTGACACAAA	84708
rs566706513	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53601549	ACCTGCCCATAAACT[C/T]GCAGCAGCTGTGACA	84708
rs566763920	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53488008	TCCATCTTGTGCTCA[C/T]AAAGCCCTGGGAAAT	84708
rs566823277	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53579602	GCCTGCAACCAAGAG[A/G]GTCATTCGAGATCGT	84708
rs566853675	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53552130	GGAAAGAGCGCATCA[C/T]TTCCTGGCTTCCTGG	84708
rs566862223	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53614625	ATAGGTCTTAGAATT[C/T]TAGACTTGCCTAAGT	84708
rs566884785	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53589814	GTCAATCTGACTCTG[A/G]ATTCCAGTCTTTGTC	84708
rs566889903	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53589965	AGCACTAATCAACCA[C/T]GGTAAACCAGAGGCA	84708
rs566897822	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53478471	GATCACTCCCACATT[A/C]TCTCATTAATTTTGA	84708
rs566903418	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53516148	TCAGGAGGCGGAGGC[A/G]GGAGGACTGCTTGAG	84708
rs566909613	in-del	-/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53646225	ATTTTATGGCAGAGC[-/T]CCAACTCTGAGATGC	84708
rs566912677	in-del	-/AAAT	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53532440	GATAGACTCCATCTC[-/AAAT]AAATAAATAAATAAA	84708
rs566961276	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53493380	ACCACCTTGGAACTG[A/G]GACACCACCAAGTGG	84708
rs566966952	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53583442	GGTCGTGGTTAGCTC[C/T]GCTTCTGCTTAATTT	84708
rs566982016	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53467966	GCAAGGCAGGCCAAC[A/G]TTCAAATTCAGGAAA	84708
rs567027609	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53462055	AATAAATGAATTCGT[A/G]TACTTTTTTTGACCT	84708
rs567044864	snp	A/C	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53467711	ACAAGCCTCAGTAGC[A/C]GATGCGATCAACTGG	84708
rs567044938	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53561877	CAAACCATCATGACA[C/T]ACATACACCTATGTA	84708
rs567045438	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53570541	AGGGGGGAGGGATAG[A/C]ATTGGGCGATATACC	84708
rs567061005	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53472459	AACCTGCACGTTGTG[C/T]ATATGTACCCTAAAA	84708
rs567068335	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53515770	AAGATGGCACAGCAC[A/G]GAGGAAAAAGCACAT	84708
rs567088914	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53611437	TTACTAAAAATCACA[A/G]CAAAGTGGGTATTTC	84708
rs567090892	snp	C/T	0.000399281	0.0141238	nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53604044	TAAATGGAAAGCAAT[C/T]GATTTCTGATAGTCA	84708
rs567092580	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53468004	AATGCCACAAAGATA[C/G]TCCTCAAGAAGAGCA	84708
rs567095633	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53487505	AAGTTAAGAAAGTTA[A/C]GAGTTGCCACCCTCT	84708
rs567118000	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53597508	CTGGCCATGTTCCAC[C/T]CTTCATTCTCTCTGT	84708
rs567121786	snp	C/T	0.0107246	0.0724382	intron-variant	LNX1	GRCh38.p7	4:53472253	CAAAAAACCAAATAC[C/T]GCATATTCTCACTCA	84708
rs567129603	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53610877	TTATATAAAAACATC[A/T]AAACTCTATACATGT	84708
rs567157918	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53570022	GGAAAGAACAGGTGG[C/T]GGAGAGGATGTGGAG	84708
rs567183312	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53633069	TGTCTGGGTTCAGCC[A/C]CAACATCATCACTTT	84708
rs567184124	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53479145	CTCCAAGTGCCTTGG[C/T]CTCCCAAAGTGCTGG	84708
rs567190517	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53521857	CAGGCTGGAGTGCAG[A/T]GGCATCATCATAGCT	84708
rs567253158	snp	G/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53543297	CTTTATTTATTTCAT[G/T]CCACTTATTTCCATC	84708
rs567263821	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53536306	ACCTACCTCGCAGTG[C/T]GAATGAACAGATTCT	84708
rs567270669	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53472189	CATGTCCTTTGTAGG[C/G]ACATGGATGAAGCTG	84708
rs567275949	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53562889	TTGTACACCATACAC[A/G]TATACAATATGTATT	84708
rs567303056	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53549990	CCTCCCTAGGAGGAG[A/G]ACACTTTGGACCAGG	84708
rs567310402	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53637774	GAAGGAGTGTCTTAG[A/G]ATTAATGAAATATGG	84708
rs567315719	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53556149	TAAATCCAGTGATAA[A/G]TTTCCTTATAAGAAG	84708
rs567331793	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53586596	CCCCGGTTAATTGGG[A/G]TAGAACTTGCTCCCA	84708
rs567337797	snp	A/G	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53625361	ATATACAGAACTCTT[A/G]TAACTCAACAATAAA	84708
rs567344945	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53643616	AACTAGCTGCCCAAG[A/G]CCTCTCGCCCTCTCT	84708
rs567358994	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53524612	AATGCTTTAAGCCTA[C/T]GCTCTTTCTAGAACC	84708
rs567360636	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53554288	ATTTGCCAGTTCTGG[A/G]TCTGCTCTTCATCCT	84708
rs567376577	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53632066	TTGAATCTTGACCTG[A/G]AGTGGAGGGAGGTGG	84708
rs567386074	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53637046	TTAGGACTGAATTAC[A/C]GCCTCAATTGTTTCA	84708
rs567400220	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53515732	CATTTTTCAATAAAC[A/G]CTCATGGGAGGGTCT	84708
rs567409733	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	LNX1, LOC101928879	GRCh38.p7	4:53576837	TTTCCAAATAAAGTC[A/G]GAGGTTGTTTGTGCA	84708
rs567431105	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53466347	AAATGATCGTAAAAA[A/T]TATGTTTAAAAAGAA	84708
rs567455176	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53463180	CATCAAAAATATTAC[A/G]TGTTCTAGTTCAAAG	84708
rs567495593	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53502454	CTCAATTTAAAAATA[C/T]TTTATTGCTAAAACA	84708
rs567519101	snp	C/T	1.66208e-05	0.00288273	synonymous-codon, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461500	GAAAAAAGGTTTGTT[C/T]CCATTGTATTCTTCA	84708
rs567546413	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53528056	ATTGCCCATGTTTAA[C/G]TGTTTTCCAGTCTGT	84708
rs567555138	snp	C/T	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53569996	TTAGAATGGCGATCA[C/T]TGAAAAGTCAGGAAA	84708
rs567567610	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53638326	TAGCAAGACTGTACA[A/G]TATAGGTATAGTCAA	84708
rs567579437	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53498070	GAGGACAGTAACACC[C/T]AAAGCATTCTATTCC	84708
rs567589964	snp	C/G	0.00478085	0.0486577	intron-variant	LNX1	GRCh38.p7	4:53623198	GAGCGTTTGCGTTGA[C/G]AGCAATTCTTTTTTT	84708
rs567605377	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53582515	TGTGACATTTTACAA[A/C]CAGTGTGAGGCTCTG	84708
rs567615336	snp	G/T	0.0185938	0.0946107	intron-variant	LNX1	GRCh38.p7	4:53568787	CAGCCCAAAATCTCC[G/T]TAAGCTGATAAGCGA	84708
rs567634072	snp	G/T			intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53559504	CAGTAGGCATGTTTG[G/T]TTAACCTCTCTGAAC	84708
rs567650825	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53623767	CTAGCAACTTGATTA[A/G]GTAGGTCTATTATTG	84708
rs567653073	in-del	-/C	0.00119737	0.0244387	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53513309	AAGCCTCCCACTTGT[-/C]CTATTAGTTATACCA	84708
rs567708336	snp	A/C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53616969	CCCATAAGCTACAAT[A/C/T]GTCAAAGCTTTTAAA	84708
rs567709798	snp	A/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53649088	CAGTAAGGCATAAAA[A/T]GAATCCAAAAGGTTC	84708
rs567719092	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53614640	TTAGACTTGCCTAAG[C/T]TGTGAAATTCTTTAG	84708
rs567724955	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53539105	TAGGTTAAATTTCCT[A/G]GATAAAATCAGATCA	84708
rs567728970	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53532332	AATACAAAAATTAGC[C/T]GGGCGTGTTGGCACG	84708
rs567738507	snp	C/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53596711	TAAAATGTCTCTTCT[C/T]CTTGTTAACTTTGAC	84708
rs567747546	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53466609	AAAGGGGTGACAGAC[A/G]GCACCTGGAAAATCG	84708
rs567756565	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53589190	GCCCATGGAGAATCA[C/G]ATTTTGTGGGTCTGT	84708
rs567788872	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53477053	CTTAAAGTGCAAGGG[A/G]ATAGGGGCTGACTGG	84708
rs567792251	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53588684	CATTTTAGCGTCCTT[C/T]GGGGAAAAATGTAGC	84708
rs567800014	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53478812	TGAATGTAGAAAATG[C/T]AAAGTGGGTTTCCAT	84708
rs567800625	snp	G/T	0.00119737	0.0244387	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53594507	AAGAATGGTTTAGAC[G/T]AGGCTTGGCAAATCC	84708
rs567817340	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53640243	GACTGTCAGGAAGGC[A/G]AGGAAGCACTGCCTA	84708
rs567819659	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53633022	TGGTGGGGAGTTCGG[A/G]GTGGAAAGAACATAA	84708
rs567857258	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53533247	TTGCAAATGAAGAGA[A/G]GTCCAATAGAACATA	84708
rs567866145	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53652002	CTTTTAGACTCTCCT[C/T]AATTTGATGTGTGTG	84708
rs567881404	snp	G/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53515547	GACAAGAAGACCGAC[G/T]TAAGAAACTGATCTT	84708
rs567882171	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53617328	AGCTTTCATTTTTGA[A/G]GGTCACAGCAGTAAA	84708
rs567885331	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53471733	CAACAGACACATGAA[A/C]AAATGCTCATCATCA	84708
rs567919273	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53579891	TTACGTGTTCTTCCC[A/G]TTGAAAGGACAAGAT	84708
rs567945971	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53559036	ATTCCATTTTGCCAA[C/T]TCAAGACCAGAATCT	84708
rs567948162	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53478451	GGGTAACAAAAGTCC[C/T]GGCCGATCACTCCCA	84708
rs567964742	snp	C/T	0.000399281	0.0141238	intron-variant, missense	LNX1, LOC101928879	GRCh38.p7	4:53575605	GATTAAGAATCCCAC[C/T]TTGGGACCAGGCCCG	84708
rs567989765	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53538472	GCATGAGACTAGGAC[A/C]CCTGCTTTTTTGAAT	84708
rs567999337	in-del	-/A	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53584040	TAGGAGTCACCAAGG[-/A]TCCCGGGAAGAGCTG	84708
rs568066758	snp	A/G/T	0.000120366	0.00775694	intron-variant	LNX1	GRCh38.p7	4:53496416	GCAGGTGGAACAATC[A/G/T]TGCGGTCAGCTCCAC	84708
rs568082040	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53620052	TGGTCTGTTTGTAAC[A/G]AAACACATTGTGGCT	84708
rs568100241	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53612733	GTAGAGATGGGGTCT[C/T]GCTATATTGGGTATG	84708
rs568130847	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53533888	CAAGCATCTGTGTTG[C/T]TGACAAACTCTCCAG	84708
rs568140539	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53612222	CTAAAATTGTAAAGA[C/T]TTGTAACACTTATTG	84708
rs568151760	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53489541	AGGATATCTAGAAGT[C/T]ACTCTCATGATTATG	84708
rs568153810	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53586286	AGCCTAAACATGCTG[C/T]GCTCTATTCAGAAAA	84708
rs568160318	snp	C/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53500011	AAACAGCTGCTCTAA[C/T]TGTCCTGCTGCTTGA	84708
rs568175890	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53592748	GGTTTGGTTTGGGGG[A/C]GGGTGGAGGAAGAAG	84708
rs568176974	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53619047	TGAGCCACTGCACTC[A/G]ACCTCACTTTAGTCA	84708
rs568199725	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53469969	CAATAGAAAAAGAGG[A/G]AATCCTCCCTAACTC	84708
rs568205839	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519700	GCACACACACACACT[A/C]CTTAACAGGCGTCAG	84708
rs568282981	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53475958	ACATCTTAGCAAAGG[C/T]GAAGTGCTCTGGGGC	84708
rs568284138	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53613879	GGTCTTTGAGCAATC[A/G]CCACACTGTCTTCCA	84708
rs568305115	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53621411	CCAGGACAGGGAGAC[G/T]GTTTTATTTTTCTCT	84708
rs568325388	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573418	TTTTATTAGAATTTT[A/T]AAAAATCCCATAAAC	84708
rs568359002	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53639837	AGGGATTTGAGACCT[C/G]CCTGAGCAACATGGT	84708
rs568365666	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53525284	GTCAGGAGTTTGAGA[C/T]CAGCCTGGCCAACAA	84708
rs568373600	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53482625	AAATCAAATACTGCA[C/T]GTTCTCACTTGTAAG	84708
rs568393001	in-del	-/A	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53550076	ATTCTCAAAGGGGGG[-/A]AAAAATAAAATCATG	84708
rs568393993	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53650492	TGTCAGAGAAGGGAG[C/T]TACAAATGTGGAAAG	84708
rs568427241	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53605582	CTTGGCCTACATAAC[C/T]CTGTCCTCTCACCCC	84708
rs568447603	in-del	-/AAAGA			intron-variant	LNX1	GRCh38.p7	4:53541160	AGAAAAAAAAAAAAG[-/AAAGA]AAAGAAAAGAAAAGA	84708
rs568451970	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53630174	TTCCAGGAGCTCCTG[A/C]TTAAAACAGGGACTT	84708
rs568457041	snp	A/G	0.00159617	0.0282053	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53517802	GTTATGAGCATTTTT[A/G]CGTAGTCAGAGGTGA	84708
rs568457349	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53571317	AGCCTCCATGCCCCG[C/T]GTAAATTAAGAATCT	84708
rs568465431	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53540783	TTTAAGTATCCTCAC[G/T]TATTGGGGTCAAACA	84708
rs568491750	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53530950	AGGAGGTATTGCTTG[A/G]GCTCAGGGGTTTGAG	84708
rs568501170	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53563397	TTTTCTAAATTCAAG[A/G]GTCTCCAGAGGTATT	84708
rs568539760	snp	C/T	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53473184	AACAAGAGCTCAATG[C/T]AGAGATAAGACTTCA	84708
rs568542694	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53545287	AAACTACCCAATCAT[C/T]ACCCAGAAAAGTTGA	84708
rs568547863	snp	G/T	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53570695	AAATAAATAAATAAA[G/T]AAAAGAAAAATATTT	84708
rs568555213	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53545241	ACAAACTAGGAACTG[C/T]CATCTTCAGCATAAT	84708
rs568562332	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53562909	CAATATGTATTTGTC[A/G]ATTAAAAAAATAAAA	84708
rs568565851	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53544733	TGGACACGTAAGTAG[C/T]TGACACTGATCAATA	84708
rs568645290	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53583902	CATTTCCTAGTCCAT[A/C]AACATGATGAAATAG	84708
rs568682682	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53468749	AGACAAAGAAGGCCA[C/T]TACATAATGGTAAAG	84708
rs568697767	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53469104	AGTAAAGCACTCCTC[A/G]GCAAATGTAAAAGAA	84708
rs568704045	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53607791	ATAGACCAACAGAAC[A/G]GACAGCCCAGAAGTA	84708
rs568709427	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53585277	ACACTTACTACTGTG[G/T]CATGAACATAGAAAT	84708
rs568710395	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53614428	TCTCTACCTCTATCC[C/T]TTCTCATCCATACTT	84708
rs568712750	snp	G/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53594520	ACTAGGCTTGGCAAA[G/T]CCTGGACATATAGTG	84708
rs568714582	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53503723	CACCAGCTGTATTAG[A/C]CCCGAACAAGAGAGC	84708
rs568728374	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	LNX1	GRCh38.p7	4:53558126	CACGTTAATAAATCA[C/T]GGGCCCGTAAGAAGA	84708
rs568760152	snp	A/C	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53463869	TAATTTAGTCAATAC[A/C]TATTTGAGAACACTG	84708
rs568773069	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53637113	GAAGCAGTTTGATGA[C/G]AGGAAACCCAATTTG	84708
rs568775953	in-del	-/GTT			intron-variant, upstream-variant-2KB	LNX1, LNX1-AS2	GRCh38.p7	4:53591100	TCTACTTCTCTTTAG[-/GTT]GTTGTTGTTGTTGTT	84708
rs568786928	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53484544	CTCAAGCCTGGGTGA[A/G]AAAGCAAGACTCCAT	84708
rs568796330	snp	A/C	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53632947	CTATGTACAAGAATC[A/C]TTTTGTAGGTTCTAC	84708
rs568816012	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53531190	TCAGCTGAGAGGTTT[C/T]CCCCACCCCACTACT	84708
rs568867987	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53492007	GACCAGGCTGGTCTC[A/G]AACTCCTGACCTCAG	84708
rs568870977	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519711	CACTCCTTAACAGGC[A/G]TCAGGCTATTCTGAG	84708
rs568875335	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53537972	GGGGAGAGAGCCTTG[A/G]CTACTGTCAATAATT	84708
rs568908047	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53625583	AGAAGGATTGCTTGG[A/G]CCCAGGAATTTGACA	84708
rs568921485	snp	C/T	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53584893	TGCCTTTCAGTGTAA[C/T]GTATATCACATTTGC	84708
rs568926677	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53618099	AACAACTTAGCTTCT[C/T]ACTGATAGACAGTCT	84708
rs568959251	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53495920	GAAAGGGAGGCACTG[A/C]ATGACACATGTGGTA	84708
rs568961353	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53592077	GTTTTCAAACACTTT[A/T]GCGCTACCCCCTCCC	84708
rs568988588	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53651012	GGATGTATTACCATC[A/T]TTCTCATTTTACATA	84708
rs568989116	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53474643	TATTCTGTTACTACA[A/G]GGAGAGGATGGAATG	84708
rs569009317	snp	A/C/T	0.00398731	0.0445001	intron-variant	LNX1	GRCh38.p7	4:53606108	AAATCAGAGCTGAAC[A/C/T]GAAGGAAACTGGGAA	84708
rs569019273	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53532608	CATTTTGATAGTCCC[A/C]ATAGGAAATTCTCCT	84708
rs569019998	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53616310	TACCATACACTTAAA[A/C]GCTCATAGGAGACAA	84708
rs569026016	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53532133	TCTTAAGAAAGGGAT[A/G]GACCAAGGACACAAA	84708
rs569050776	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53481646	CAGAGATGACACTTA[A/G]ACATGTTAAAACAAG	84708
rs569063880	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53525401	GCAGGAGAATCGCTT[C/G]AACCTGGGAAATGAA	84708
rs569072817	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53578993	ATGTATGATGTATCA[C/T]GTTTTCAGACATATC	84708
rs569088157	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53620515	CAGACACAGTGTTAG[C/G]TGTTGGGTGCATTCG	84708
rs569094898	in-del	-/A	0.15698	0.23205	intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53559813	CCGCCATGCCTGGCT[-/A]AAAAAAAAAAAAAAA	84708
rs569130766	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53516944	TCCCTGACCATCAAT[C/T]CAAAGTGAACTGCTG	84708
rs569139957	snp	C/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53481153	CTGAAGAATGAATTC[C/G]ACCCACAGATCCACA	84708
rs569155340	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53644866	AGAGTAAGGGAGAGA[A/T]GTGGTAACAGGGAGG	84708
rs569159344	snp	A/C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53644634	GGGAACTCATAGGCT[A/C/G]TCCTATTCCAGGAGG	84708
rs569189735	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53555204	GCAGGCATCACCCAT[C/T]ATTCCTGCTCCCAAG	84708
rs569191564	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53650446	TAAGCAAATAATATA[C/T]TAAGGATAATGGGAG	84708
rs569210642	snp	A/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53611561	AATAAGTAGAGATGG[A/T]GTAAGGGACATCCTC	84708
rs569221191	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53537047	GAGCCACTAGGCATG[C/T]CATTAGGTGAAAAGA	84708
rs569227509	snp	C/T	0.0023933	0.0345097	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53503191	AAAATCAACTTCCTC[C/T]AAACTCCTGTTAATG	84708
rs569230651	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53650140	TGCTGAGGACACGTG[C/T]CCTGCCTGTATGGAG	84708
rs569248943	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53487281	AAACGTACAGGGGGA[A/G]TAAGAACTGGTCAAG	84708
rs569258287	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53590008	GGAGAGGTTTAGATG[C/T]ACTTTTATCAGAAGA	84708
rs569266820	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53579393	ATATGGAGCCAAAAC[C/T]CCCAATCTAGTGCTG	84708
rs569303324	snp	A/G/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53520063	ATGTTCTGTCCCCAC[A/G/T]TTTAGTAGAAACAGA	84708
rs569311252	snp	A/G	0.0107246	0.0724382	intron-variant	LNX1	GRCh38.p7	4:53570611	ATGGCACATGTATAC[A/G]TATGTAACTAACCTG	84708
rs569322338	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53463702	CCAATGAGAAAATTA[C/T]GGTTACCTCAAGAAC	84708
rs569330914	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53479226	CAGAGTGAACTGCAC[C/T]CAAAATTTCTCAAGT	84708
rs569332689	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53623471	ACACATGAGCTCAGG[G/T]GATCCACCTGCCTTG	84708
rs569350303	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	LNX1, LOC101928879	GRCh38.p7	4:53576728	AGACCTTATGCTTTC[C/T]ACAAGAACATAAAGA	84708
rs569356172	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53605485	AATTTCCAGTATACA[A/G]TACAATATTTGTAAC	84708
rs569361880	snp	C/T	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53622463	TGTCAACCTGATTGG[C/T]GTGGCGAGACCACAG	84708
rs569373033	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53570071	ACTGTTGGTGGGACT[A/G]TAAACTAGTTCAACC	84708
rs569378107	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53557422	ACATTTTATACATAG[A/G]GTTCTTTTTTTACTG	84708
rs569394693	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53502872	CTTTATTTGCTCATC[C/T]GTAAGAAATGCCTCT	84708
rs569439734	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53563252	TTAGATGCATATTTA[C/T]TGAGTAAAGTGATGT	84708
rs569441019	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	LNX1, FIP1L1	GRCh38.p7	4:53462963	AGCAGGTAACTGGCT[A/G]TTCTGTAAATACCAA	84708
rs569441665	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53598480	CCAAGCGATCCTCCT[G/T]CCTTGGCCTCCCAAA	84708
rs569477649	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53620602	CTTGATGGGTACAAC[A/G]TGCATTGCTCCACTG	84708
rs569490796	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53612123	AAGGGTTGAGAAACT[C/T]GGAAATATCCTCAAA	84708
rs569515942	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53468694	GGGTTGCAATCCTAG[G/T]CTCTGATAAAACAGA	84708
rs569523220	snp	A/G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53556946	GACTGTAATTTACAC[A/G/T]TAAGCCAACTCTTGC	84708
rs569528441	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53468367	TGGAAAGGAACAACC[A/G]TTACCAGCTACTGCA	84708
rs569576591	snp	A/T	0.000399281	0.0141238	nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53604717	AAGTCAGAGACAGAC[A/T]AATTTGTTTCTCATA	84708
rs569639055	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53527097	CAAAACCTGACCCAA[C/G]CTTGTGTGTATAAAC	84708
rs569648311	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53513460	TCCCTGATCCCTAGA[C/G]TCATATCAAACTGCC	84708
rs569659955	snp	C/T			intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53559838	AAAAAAATTAAAATC[C/T]TTTTCAGAGATGAGG	84708
rs569668597	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53586386	TTTAGACCTCCCCAT[C/T]ATGCATGTGCTATTG	84708
rs569696667	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53610647	CGGGAGGCAGAGCCT[G/T]CAGTGAGCCGAGATC	84708
rs569700472	snp	C/G	0.00398564	0.0444627	intron-variant	LNX1	GRCh38.p7	4:53534421	AGGCAGGAGGGTCTC[C/G]AGCCTAGGAGATCCA	84708
rs569701331	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53470617	GCCCAAAATCTCCTT[A/C]AGCTGATAAGCAACT	84708
rs569710388	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53574227	GAGGGTCCACTCTGG[A/G]GTGACTGACAGGACC	84708
rs569711152	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498940	AGCCAAACTAAACTA[C/T]TCATTTTTCCTCATA	84708
rs569734958	in-del	-/G			intron-variant, downstream-variant-500B, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460244	GTTACTAACGATTGT[-/G]GGAAAAAAAGAGCTT	84708
rs569741159	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53528239	TAAGAAATACATAGT[C/T]CTCCCTTATCCATAG	84708
rs569747394	snp	C/T			upstream-variant-2KB	LNX1	GRCh38.p7	4:53653795	CACTTCTGACTCTTT[C/T]TGGTTCTACCCCTAA	84708
rs569765818	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53565092	GCCTACCATTGCCCA[A/G]GCTTGATTAGGTAAA	84708
rs569770957	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507073	TCTTCCTCATATGCA[C/T]AATGGTACTAGCGCC	84708
rs569772508	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53469896	GATGGATTCACAGCC[A/G]AATTCTACCAGAAGT	84708
rs569782502	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573554	AAGCCCTCAGGAGAC[C/T]GGGGGGTGGAGGGGT	84708
rs569793275	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53630318	TTTTTGTAACCCCCA[A/G]ATCAGGATTCACGGT	84708
rs569809451	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53471187	TCAGAAATAATGCCG[C/T]ATATCTACAACCATC	84708
rs569818620	snp	G/T	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53548829	TATAGATATACCATG[G/T]AATACTATGCAGCCA	84708
rs569834541	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53469293	TTCTTTGAAACCAAC[A/G]AGAACAAAGACACAG	84708
rs569834785	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53602172	ATGAAGTTACTCTCC[A/G]AAGTGATAAGGGGAT	84708
rs569835424	snp	C/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460009	GGTACACTTTCATAT[C/G]CAAATTAATAAAACC	84708
rs569870571	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53594725	CTTTTTTAATTTTTT[G/T]TTTTAGAGACAACTC	84708
rs569889754	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53491395	TTCTCATTGATTGGC[C/T]GGCTAATGCCACCTG	84708
rs569890728	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53601570	AGCTGTGACAACTGC[A/G]TGAGCCTGGTAGCAA	84708
rs569891312	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53481320	AAAACTAAAAGTAGC[A/G]GGGAAATCACTCATT	84708
rs569897541	snp	C/T			intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461943	ATTGGTGAACAAACA[C/T]ACTTATGGATGTCAT	84708
rs569908438	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53505098	ATAAAAATGAGGTAT[A/G]CTTTTATTTTATTAT	84708
rs569911649	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53467093	CTGGGAGGCACCCCC[C/G]AGTAGGGGCGGACTG	84708
rs569950573	snp	A/C/T	0.000399281	0.0141238	upstream-variant-2KB	LNX1	GRCh38.p7	4:53653245	AGTTAAAAATGTAAA[A/C/T]GTTGCACTTCTGGAA	84708
rs569979074	snp	A/C			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53506803	AGAGGTTGCAGTGAG[A/C]CGAGATCATGCCGCC	84708
rs569980957	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53477269	GAGGAAAATTAGTCT[C/T]GTTCACTATTTAATC	84708
rs569988676	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53560257	GATCTTGGACATGTC[A/G]GATTGCTTCTGACAT	84708
rs570002335	snp	C/T	0	0	intron-variant	LNX1	GRCh38.p7	4:53490880	GTTTTTCCAACATTC[C/T]GTGTTTTCCATTTCT	84708
rs570013468	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53614223	GAAAGTTTGCTGTTC[C/T]ATTTGCCACCCTGTC	84708
rs570017617	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53553225	TGATAATTTTCAACA[C/G]GGAAAGTCAGGGTAA	84708
rs570021028	in-del	-/GTT	0.00517822	0.0506191	utr-variant-3-prime, downstream-variant-500B	LNX1, FIP1L1	GRCh38.p7	4:53460287	CTAAAAACAAAACAA[-/GTT]GTTTATAATTAATTC	84708
rs570068878	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53651344	GCACCGGACTTGCAC[A/C]ACGCCCTGACACATG	84708
rs570070541	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53639570	ATTGGCTGATGAAAA[C/T]GGTGCAAACAAAGGC	84708
rs570100621	snp	C/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53599871	TAGAAAGACTATGTA[C/T]ATTTCAGATATGGTC	84708
rs570102722	snp	A/G	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53580779	CATAATGTATATCCA[A/G]TCCTTAGAACCATTG	84708
rs570111670	in-del	-/AGCTACT	0.00676609	0.0577691	intron-variant	LNX1	GRCh38.p7	4:53476181	TGTGCCTGTAATCCC[-/AGCTACT]AGCTACTTGGGGAGG	84708
rs570129970	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53621478	CATATAATGGGTGCT[C/T]GGTCAATGTTCATTT	84708
rs570143034	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53645846	TGAAACCGTATGAAA[C/T]ACCAGACTCCTGGGC	84708
rs570146657	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53477401	GGCCTCCAGTAAATA[C/T]GGATTGAATGAAAAG	84708
rs570153172	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53475098	AAAAGTAGAGAAGTG[A/C]CATGCCCAAGGGCAA	84708
rs570166413	snp	A/G	0	0	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53511304	ATACTGGGGCAGCTT[A/G]ATTTACAAGCATTAA	84708
rs570191398	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53510809	CTGCCAGAATAGTAA[C/T]GTTATTTTCCAGCTG	84708
rs570191537	snp	G/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53627871	CATGCCCCTTTGGGA[G/T]ATTTGAAGATGAGGG	84708
rs570192575	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53518842	CATGGAAAATTAGAA[A/G]CAGGTTTTTCATAAC	84708
rs570228178	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53634739	CACAGGGACTGCTCC[A/G]AGGGGTGGCGGTTTA	84708
rs570231779	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53628434	CAAATTAAAACCATG[A/G]TGAGACACCATATTA	84708
rs570263619	in-del	-/AG			intron-variant	LNX1	GRCh38.p7	4:53524841	GAGATGCATCTGTCA[-/AG]AGGAAGGAACCCTTT	84708
rs570279455	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53534520	TTGAGGACATGCTTG[C/T]AGGCCCAGCTATTCA	84708
rs570325468	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53520030	CCATGACATACACTG[C/T]ATCTTTTTCCTTTGT	84708
rs570332852	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53613985	CTGTTATTTTTTGAC[A/G]GCCCTTTTTTGATAA	84708
rs570340794	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53474707	CAGTGTTGTCTATGC[C/T]GGGATATCATGCTTC	84708
rs570363387	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53647375	TGTTTTAGGAAGCAA[C/T]CTCTCTCTCTCTTTT	84708
rs570366311	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53641051	CCCCAGCCTTGGAGG[C/T]GACTCGGCACAGGCT	84708
rs570373016	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53505939	GATATACAGCATTTA[A/T]AGGACTGTAATAAGC	84708
rs570395790	snp	A/C	0.000798403	0.0199641	utr-variant-5-prime	LNX1	GRCh38.p7	4:53652351	GGTTAACCTGGGCAT[A/C]CCCTGCCCCTTCTGC	84708
rs570400751	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53541303	CTCTCTAAAACTACA[C/T]TGACTTGGCAAGATC	84708
rs570445134	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53482749	ACTGCCTATTTGGTA[C/T]AGTGTACACTATTCA	84708
rs570457593	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53490358	AGCTGCCTCTTTCAT[A/T]CAGTTATTCCAGTCA	84708
rs570492970	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53540022	TTTTGCTCGGGCTAC[C/T]AATCAATACCAAATC	84708
rs570493548	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53475203	TCTTACACAAATGAA[A/T]AATGAAGGACTTTGA	84708
rs570497469	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53640676	TTGTTGTCAACAGTA[A/G]GAACAATTAAGACTG	84708
rs570561980	snp	A/G	0.00358779	0.0422022	intron-variant	LNX1	GRCh38.p7	4:53631847	CAGAGTCTCTTTGGA[A/G]GTGGAGCCTGAGCCT	84708
rs570564858	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53547337	GTACCAGGCACTATA[G/T]TAAATGCTTTACATA	84708
rs570625521	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53481553	GATGGGAGACACCTG[G/T]TATCTCTCCAAGTCT	84708
rs570628731	snp	A/G			intron-variant, utr-variant-3-prime	LNX1, LOC101928879	GRCh38.p7	4:53576783	TAGCCACATTTGGAA[A/G]CAGCCCAGCAGTCAT	84708
rs570629438	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53473956	AACAGTTATTTTGAA[C/T]GTTAAGTAAAAAGAC	84708
rs570630578	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53608584	TTCAAAGCAGGATTA[A/C]CATTCGACCCAACAA	84708
rs570646307	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53559727	ATTATACCTCACTGC[A/T]GTGGTGAACTCCTGG	84708
rs570676500	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53497148	CTTAAACAAGCTTAA[G/T]CTCGGCCCTCTCATT	84708
rs570695209	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53607929	ATGCGGAAGATTGAA[A/G]CAGTACCCATTTCTT	84708
rs570707112	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53627225	GATTGTATGATGGGA[A/G]CAGAGTTTAGAGTTT	84708
rs570708592	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53511240	AGAGACAGAGTGATC[G/T]ATGAAGGTAGCAGCT	84708
rs570713511	snp	C/T	0.00358779	0.0422022	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53605476	TTCCCAGTAAATTTC[C/T]AGTATACAATACAAT	84708
rs570714293	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53470530	AAGGGCATTCAATTA[A/G]GAAAAGAGGAAGTCA	84708
rs570715726	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53566011	TGTGAAGAGACCAAA[A/T]CTACGTCTGATTGGT	84708
rs570729356	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53464832	CAAAATTTGTCTTTA[C/T]TCCTCAATGATAGCC	84708
rs570770091	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53517873	GCAAGTCCACCATCT[C/G]GTATTCAGTGTAGAT	84708
rs570787149	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53504908	AATTACAATAGTAAC[A/G]CCAAAGATAACTGAT	84708
rs570787185	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53496573	TGTTCTCTCCAAGCG[C/T]GGCCTGCAGCACCTC	84708
rs570796857	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53469216	CAACTACATGGAAAC[C/T]GAACAACCTGCTCCT	84708
rs570797640	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53512063	ATTGTCCAGTCTGAT[C/T]TGACTTCAAACAAGA	84708
rs570800798	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53611198	ATTAGCTTTTTTGTA[C/G]TCTAGGAATAAGAAA	84708
rs570808118	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53570750	AAGAATCTTTTGGCT[A/G]GGCGTGGTGGCTCAC	84708
rs570814941	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53612809	AGGATTGCCTGAGTC[C/T]AGGAGTTTGAGGCTG	84708
rs570848525	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53504230	TTCTACAATCAGCAT[C/T]TGCTGCTTCGTTACA	84708
rs570854536	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53599954	TTGAAAAAGATCTGT[G/T]CTCAGCAGGTGACAG	84708
rs570877754	snp	A/G	0.00119737	0.0244387	nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53603756	GAGAAATCTGCCCCC[A/G]TGATCTAATCACCTC	84708
rs570916597	snp	A/G	0.00358779	0.0422022	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53603075	AATTCTAAAATCAAT[A/G]CTCAGATTGGCAAAG	84708
rs570926138	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53563464	AAGGGGAGTAAGAGG[C/G]GGGCCTACTGGCCCA	84708
rs570933443	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53539258	ATGCTCGAGGCCAGG[G/T]TCTGGACCTTCTCAC	84708
rs570944816	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53650958	CAGGAAAGACTTCAC[A/G]TGCATAATCTCATTT	84708
rs570965777	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53471668	AACCCCATCAAAAAG[G/T]GGGGAAAGGATATGA	84708
rs570966562	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53592807	TCCGGATTCCCACAG[C/G]CTGGGCCTCAGCTGG	84708
rs571010914	snp	G/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53568663	GAAGTTCTGGCCAGG[G/T]CAATTAGGCAGGAGA	84708
rs571012489	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53550912	AGATACAGAAAATGG[A/G]GGCAAGCAACCTCCC	84708
rs571014989	in-del	-/G	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53649099	AAAATGAATCCAAAA[-/G]GTTCTGATTTTACTC	84708
rs571025664	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53640427	CAGTAAAAAGTAAAC[A/C]GAAAAAAATGGGGGG	84708
rs571027098	snp	A/G	0.00716266	0.059414	intron-variant	LNX1	GRCh38.p7	4:53471295	CTAGCCATACGTAGA[A/G]AGCTGAAACTGGATC	84708
rs571099387	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53624368	AAAAGTCTCATGAGA[G/T]CTGATGGTTTTATAA	84708
rs571139715	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53558712	TACAGGTTCCTGTTT[G/T]GTGAGGAAATGAGTC	84708
rs571155483	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53588536	AGCATTGCCCCACCT[A/T]GAATGGAATGAATAA	84708
rs571160951	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53511795	TGATTCACAGACGTT[C/G]TGATAGGGTATCCTC	84708
rs571169363	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53592316	ATTTCTGTCCCAAGC[A/G]TGGTGTGTGACCCTG	84708
rs571176820	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53612471	TGCAAATTAGAAAAG[C/T]TAAGTGTTTTCTGTA	84708
rs571183313	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508353	GAATTTGATTTGCCT[A/G]CCGCTATATCCTCTC	84708
rs571193003	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461078	AGATATGATTAGTAT[C/T]TTAATTCGTTGCTGA	84708
rs571193975	snp	C/G	0.00119737	0.0244387	intron-variant, nc-transcript-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53501898	ACTCCAGCCCGCCTA[C/G]TCATTGAACATGGCT	84708
rs571210877	snp	C/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53467283	GCAGCTGAGGGTCCT[C/G]ACTGCTGGAAGGAAA	84708
rs571234637	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53596725	TCCTTGTTAACTTTG[A/G]CTTCATCCTGAAGGC	84708
rs571244323	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53514919	CAAATTAGGCTAAAC[A/G]TTTTAATTTTAAAAA	84708
rs571248575	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53555508	CTTATTTCCATCTGC[C/T]TTGAATCATTGCTTA	84708
rs571257073	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53500770	TGATTGAGTTCAATT[A/G]ATGTTTAAACTACTT	84708
rs571270005	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53478397	CTAAGAAAAGTGGAA[A/C]CTGGTCTAGTATCTA	84708
rs571289943	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53514376	AGACTGGGTAATTTA[C/T]AAAGAAAAAGAGGTT	84708
rs571311676	snp	C/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53642839	GAAGAATCCCCAGAT[C/G]CCTCCCAGCCATGGC	84708
rs571340555	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53563030	GCTAACATGGTAAAA[A/G]CCTGTCTCTACTTAA	84708
rs571340775	snp	A/G	0.00159617	0.0282053	upstream-variant-2KB	LNX1	GRCh38.p7	4:53654035	CTTTGGGGGTATTTT[A/G]CCCTAAGGCTGCATG	84708
rs571349798	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53548763	ACAATAGCAAAGATA[C/T]GGAATCAAACTAAAT	84708
rs571350207	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53649021	CTTTGGAGGCTGAAA[C/T]GATAAAAAAATTATG	84708
rs571357771	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53548010	TCATAAACCTGGATC[A/C]TCCAGTTCCAATCTT	84708
rs571392569	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53521301	TCAGAGCTTGATATC[C/G]AGATGGAGGTGTGGG	84708
rs571434000	snp	A/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461877	CATATTTTTAACTTA[A/T]GACAATGCTTGAATA	84708
rs571471472	snp	A/C	0.0267878	0.112589	intron-variant	LNX1	GRCh38.p7	4:53567981	TAGACCAATAACAGG[A/C]TCTGAAATTGTGGCA	84708
rs571473630	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53555817	CTAGCATCATACTTT[C/T]ATAGATTGCTTGTGT	84708
rs571478829	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53589291	CTGTGAGGCTAGCGG[A/G]GACAAATCTGCCCAC	84708
rs571503135	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53581605	TAACATGGTGGCAGG[A/C]GAGAGAACATGTGCA	84708
rs571510738	snp	C/T			intron-variant, nc-transcript-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53500460	CTCCTTTCGTTATGG[C/T]ATCTGGAAAGATCTC	84708
rs571522663	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53529299	AGACAGGAGGACAGA[A/G]TCTGCCTGGGAGCAG	84708
rs571523467	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53463509	CTTAAGTTGGGTTAT[C/T]TCACTCCCCACTGGG	84708
rs571536958	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53477762	TATACAGAATAACCA[A/C]AGCAAGAGCAAAAAG	84708
rs571537820	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53636298	TGTCTTGAAAAAATT[A/G]GCATGCACCTCCTTC	84708
rs571577163	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53643500	AGCAGAGTGGACAGA[A/G]GGTGGCTGATGTAGT	84708
rs571592255	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53541468	GATCTAATCAGCACA[A/T]TTCATATATATTTTT	84708
rs571608426	snp	A/G	0.00398564	0.0444627	intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53575129	TGGGATTACAGGCGC[A/G]CGCCACCATGCCTGG	84708
rs571629575	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53590225	CTGTCTGTCTAAGGC[A/T]AAAATGATCTCAGCT	84708
rs571633073	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53499540	CATGGTTCTCTGCAT[A/G]TATCTCTGCATGCAG	84708
rs571656076	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53470458	CCTCTCTCACCACTT[C/G]TATTCAACATAGTGT	84708
rs571665723	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53629467	TCAAAATGTCCCAGG[A/C]CCTGCCAAAGCTTGG	84708
rs571670718	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53644359	GTGAGCCGAGATCAC[A/G]CCACTGCACTCCAGC	84708
rs571693506	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53619784	TTTTTCGATGAACTG[G/T]CAAACTGTTTTTCCA	84708
rs571693852	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53528273	TGCTTTCCGCAGTTT[C/T]AGTTACCTGTGGTCA	84708
rs571703312	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53628836	TACAATGACTTGGAC[A/G]AAGCAGGAGGCCATT	84708
rs571708772	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	LNX1	GRCh38.p7	4:53653471	TATGTATATGCAACA[C/T]GCAAGAAAGACACAT	84708
rs571717418	in-del	-/TTC			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53596444	TTTGTGGTCAGCATG[-/TTC]TTCTTTAGTAGGGAG	84708
rs571728459	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53609233	ACATGCAATTTACCT[A/G]TGTAACAAATATGCA	84708
rs571730524	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53620092	CAACTGTTTTATCCT[G/T]TCTGTGCCAGCAGCA	84708
rs571734767	snp	C/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53594780	GCAGTGGTGCCATCA[C/T]GGCTCACTGCAGCCC	84708
rs571751901	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53635109	TGCTGGAATAGCACG[C/T]ATGAGCCATGGTGCC	84708
rs571765844	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53608724	CTAAATGCCCATCAA[C/T]GGTAGAATGGATAAA	84708
rs571833653	snp	A/C	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53513044	CCAACCCTGGCCTAT[A/C]CCTCTGCCCCTGGTC	84708
rs571835289	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53618626	ATGTTCTTTACAAAG[A/G]CACTCACCCTGTTGG	84708
rs571850579	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53484283	CACTCACTCTCAGGA[A/G]CTAGGACCTTGTTTT	84708
rs571859551	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53528753	GCTGGCCTAAACAAA[C/T]TGGGTAAGTTTACCT	84708
rs571871729	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53527946	ATGGTCTAATAAAGT[C/T]TACTTTTTCTTCATT	84708
rs571886223	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53535447	TCACTCTGCTTACCT[G/T]CAAGGGTACATGACA	84708
rs571896050	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53491512	GCATGGTACCACACA[C/T]CTCTTGGCACAAAGA	84708
rs571900777	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53485043	AGGAAACAATCGTGA[A/C]GAAAGCTGACATGAA	84708
rs571916900	snp	A/T	0.00358779	0.0422022	intron-variant	LNX1	GRCh38.p7	4:53650168	GAGGAGACAGCTTTG[A/T]CCCCCATCAAAGACA	84708
rs571922619	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53623150	GCTGGACTATATGTG[A/G]GCTAACATCTTCTTA	84708
rs571927155	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53622471	TGATTGGCGTGGCGA[G/T]ACCACAGCTCCCCTT	84708
rs571944046	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53581991	AATATTGCATTCACA[C/T]TAGGATTACTGAATT	84708
rs571973285	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53492786	GCCTAGGGGAGAGCA[C/T]GTTGGGCAAGGGGTG	84708
rs571978240	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53629029	ACATTAGGTACAATA[C/T]ACACTACCTGGGTGA	84708
rs571979964	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53636542	TCAGGTCCTTGAACC[A/G]TAAAATGGAGATGAT	84708
rs571985740	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53518848	AAATTAGAAGCAGGT[G/T]TTTCATAACCTTATA	84708
rs571993149	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53594858	CTGGGACCACAGGCA[C/T]GTGCCACCATGCCCT	84708
rs571993565	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53551416	AACTGGTGATCAGCT[C/T]CCTAGTAAGATCTCA	84708
rs572003143	snp	A/G	0.0178098	0.0926698	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53601100	GAAAGAAAGGGAGGG[A/G]GGGAGGGGGGGAGGG	84708
rs572030275	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53641455	GAAGAGGAATGGCTA[A/C]AACCTCTGTGCTCAG	84708
rs572058428	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53466386	ACAGCCGAATAGGAA[C/T]AGCTCCAGTCTACAG	84708
rs572079572	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53580212	CTATACCTCACCTGC[C/T]CTTTCCACAAGTGCC	84708
rs572158494	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53588766	GCAAGCTAGTAGAAC[A/G]GTAGAACCCACTGAC	84708
rs572162089	snp	G/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53595344	CTGAGACTGTAAAGA[G/T]CCTCGGGAACCTCAA	84708
rs572174039	snp	C/T	0.00676609	0.0577691	intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53559893	TCTTGAACTTTTGGC[C/T]TCAAGCAATATTCCT	84708
rs572178694	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53622761	ATTGGGAAAACACTC[A/T]CTGCTGGAAAGATGA	84708
rs572184157	snp	A/T			missense, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498654	ACCTTTAGAATGATG[A/T]CTCCTGGCAGTAGCC	84708
rs572194229	snp	A/G	0.000798403	0.0199641	nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53604157	TGACAATTTGAAGTT[A/G]CCAAACTGCTGATTT	84708
rs572194396	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	LNX1	GRCh38.p7	4:53652489	TTCTGGTTTGGATGG[A/G]GCTGAGACGCCCCTG	84708
rs572198939	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53623499	TTGGCCTCTCAAAGT[G/T]TTGGGATTACAGGTG	84708
rs572301930	in-del	-/TT	0.00318978	0.0398085	intron-variant	LNX1	GRCh38.p7	4:53465992	TTTAATTAAATACTC[-/TT]TCAAAAAATTATTTT	84708
rs572302426	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53608115	AACAAAAATTGACAC[A/G]TGGGACCTAGTTAAA	84708
rs572303116	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53625888	GTGTGTGTGTATCCA[A/G]GAAAACTGAAAATAC	84708
rs572305027	snp	A/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53600356	AGGCAAAAGCCAGAG[A/G]AGAATTGTTTTGCTG	84708
rs572322373	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53548188	TCCTTGGCCTGCCAA[A/G]TTTTATTTGGCCTGC	84708
rs572330993	snp	A/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53476296	GAGCAAGACTCTATA[A/T]AAAAATAAAATAAAA	84708
rs572345526	snp	A/C			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53504221	TGCTGCAGCTTCTAC[A/C]ATCAGCATTTGCTGC	84708
rs572368883	snp	C/T	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53624203	TTCCAATCATTAGCC[C/T]ATTTCTCTCTTATGT	84708
rs572374557	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53613731	TATTTAGGTTGATTC[C/T]ATGTCTTTGCTATTG	84708
rs572393108	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53483655	GTTTAGGGACAAGGG[A/G]GATGGAAGAGAGAGG	84708
rs572419113	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53587994	GTCTTTGGCCCTCAA[C/T]GTACTACCGTTTCCA	84708
rs572461704	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53546536	TTCCAAAAAAATGTC[A/T]TAACTTGTTCAAGGT	84708
rs572483462	snp	A/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53626881	CCCATCTGTGCCAAC[A/T]GTCTGAAATGGAAAT	84708
rs572485135	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53496803	AGCTCTTCAAGCCGA[A/G]TTGACATTTTCTTCC	84708
rs572491731	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53472051	ACTTATGTTTATTGC[A/G]GCACTATTCACAATA	84708
rs572518970	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53539407	TCTCACTCTGTCGCC[C/T]GCCTTGGAGTGCAGT	84708
rs572532948	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53538909	AACTTCTGGAAGTAA[C/T]CACAGGGAACAAGCC	84708
rs572564522	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519338	CAGGAGGCCAACTTA[A/C]CCATCTCCCACTGGG	84708
rs572567233	snp	C/T	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53565341	GTGGGTCCCTGACCC[C/T]TGACCCCCGAGCAGC	84708
rs572612642	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53526878	AATCTCCAGCAGCTG[G/T]CTCCACAGAAGGCTC	84708
rs572617150	in-del	-/CT			intron-variant	LNX1	GRCh38.p7	4:53561781	TTATTGAACAATGAA[-/CT]CTGTATTCATACTAG	84708
rs572626509	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53525852	GTGGGGAGGCACTGG[C/G]AAGCTAGGCTGGGCT	84708
rs572630718	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53564860	TCAGGGAGTTAGTTC[C/T]CTTTCCTAATCAAAG	84708
rs572650820	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53583126	TAGTAAGACTTGACA[C/G]GATCGATAATGTGCC	84708
rs572655901	snp	A/C	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53620975	GTTGTTACTCCTGTT[A/C]GTTTCAAAGAGAATC	84708
rs572681259	snp	C/T	0.000399281	0.0141238	nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53605051	AGTGGAAGCTGCCAG[C/T]TCAGTTAAGGGCTAT	84708
rs572683813	snp	A/G	0.00636936	0.0560724	intron-variant	LNX1	GRCh38.p7	4:53573214	GAGACAAAAAGTGGA[A/G]TGGTGGCTGCCAGGG	84708
rs572694542	snp	C/G/T	0.00086997	0.0208391	synonymous-codon, missense, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573703	GCAGGTCACCAGTAG[C/G/T]TTGTTGAGGAGTTTG	84708
rs572699651	snp	A/G			nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53605196	CAAAGTCACATTGAA[A/G]AGCATGTGGAATGGG	84708
rs572729731	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53473290	AGCAATGAAAGTGGC[A/T]GCAAAGGAACAGAAA	84708
rs572774976	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53651696	TCACAGCTTCTCTCA[A/G]CCTCTTTATCCATGG	84708
rs572779607	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53469381	TGAATGCTCACAAGA[C/G]AAAGCAGGAAAGATC	84708
rs572791834	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53472663	TGAACAATGATTTAT[A/T]CAACAACAACAACAA	84708
rs572804300	in-del	-/A	0.00793154	0.0624729	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461045	AATATCACCACATCT[-/A]AAAAAAAAAACAAAA	84708
rs572807733	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53479371	TTCACACCTGCTCAG[C/T]GCTTACCAGGCAGCC	84708
rs572827609	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53494655	ATAAAGTCCAGCTTT[C/T]CTGCCACACTGGAGG	84708
rs572858052	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53637859	ACGGAGATTAGACCA[C/T]CACTCAAAGTCGCAC	84708
rs572863403	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	LNX1	GRCh38.p7	4:53654224	TTTATGGACTCTGGT[C/T]TTGGAGTTCTTTGAT	84708
rs572870887	snp	G/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53625014	CAATTGTTTTAAAAA[G/T]ATTTATATATTTGTG	84708
rs572874024	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53486295	CAATCGGCAGAGCGC[A/T]CTACAGCCCCAGAGC	84708
rs572879699	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53505801	CACCTAAAAAGGGGG[C/T]TGAGGGAGTGAGGTT	84708
rs572881268	snp	C/G	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53554017	ATCTATGAGAAACAG[C/G]TTAGCCCCTAGCCTG	84708
rs572908928	snp	A/C	0.00517822	0.0506191	intron-variant	LNX1	GRCh38.p7	4:53542636	TAGACATGGGTACAT[A/C]TGCAATTAGAGAAAA	84708
rs572914965	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53562988	GGCCGAGACGGATCA[C/T]GAGGTCAGGAGATCG	84708
rs572925475	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53536237	TTCTCAGGTCAGTCT[C/T]TTAGTGGAAATCCCA	84708
rs572942018	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53586694	TTTCAGATGGATAGG[C/T]GAAGAAGGGCAAAGG	84708
rs572952459	snp	G/T	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53516629	GCAGGTGCATGGCAG[G/T]TGCCAGGAATGGTAG	84708
rs572965366	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53528163	AAAACTGCTCTTTTG[C/T]CAGTTGGAAGAACTG	84708
rs572982261	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53630499	TTTTTTCTTATTTTT[A/G]TGCTTTTTCTTGGTG	84708
rs572990412	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53467490	AACAAAGCTGAACAG[A/G]GAATGACTTCAACAA	84708
rs573000947	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	LNX1	GRCh38.p7	4:53653590	CAAGGAAGTACACTG[C/T]AAATCCCTTGGCCTC	84708
rs573008390	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53618482	AAAAACTGGAAATAT[C/T]CATTGAATTGGCCTG	84708
rs573023893	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53468250	CCAAAATAAGCTCTA[C/T]AAGTGAAGGAGAAAT	84708
rs573030933	snp	A/G	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53570799	TTGGGAGGCTGAGGC[A/G]GGCGGATCACGAGGT	84708
rs573056734	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53522057	ATCTCGATCTCCCAA[C/T]TAGCTAGACTACCAG	84708
rs573076198	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53522527	TTACATATTGACACA[A/G]AGAGTTGCATGGATG	84708
rs573095864	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53479618	AGAGGAGGAGAGTTA[C/T]GTATGAAAGAGATGA	84708
rs573120891	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53568881	TAACAGACAAACAGA[C/G]AGCCAAATCATGAGT	84708
rs573130125	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53570267	TTGGAACCAACCCAA[A/G]TGTCCAACAATGATA	84708
rs573138484	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53530650	AGAATTCAGAGTAAA[A/G]AAAGTAGTATTATTT	84708
rs573155391	snp	C/T	0.00478085	0.0486577	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53521458	ACAGGCCCTCCTGGA[C/T]ATGCTGCATGACACT	84708
rs573167569	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53485076	ACGATGGAATTAGCT[A/G]ACTAAATCCAATTCT	84708
rs573194066	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53555689	TAGCATCGGGGAACA[A/G]CTGCACAGAATTCTC	84708
rs573206382	snp	C/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53555182	AGAAGGCCTCCATCT[C/G]GGACATGCAGGCATC	84708
rs573220794	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53649142	TCAGAGTTTCTTTTA[C/T]AATGCCAAAATCTAT	84708
rs573225081	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53620962	AAATTCAATTATAGT[G/T]GTTACTCCTGTTAGT	84708
rs573271187	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53610249	ATTCAATAAATAAGA[A/C]AAAATTATCAAAAGG	84708
rs573308105	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53609669	TATTATAGTACTATT[A/T]TACTATTATAGTACT	84708
rs573311184	in-del	-/C			intron-variant	LNX1	GRCh38.p7	4:53590075	CAAGTGGTGGCCAAA[-/C]CCCCCCCCCTTAAAC	84708
rs573316329	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53525545	TCTATTTTGACCTCA[G/T]CAGAGCTTAGAAATA	84708
rs573321991	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53575298	AGATATTTCTTTTAA[A/T]CAGTAGAATACTACC	84708
rs573342932	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53596941	TTCATTCGGATTTTT[C/T]ATTCCCTTCCTCAAA	84708
rs573406338	snp	A/C	0.000798403	0.0199641	intron-variant, missense	LNX1, LOC101928879	GRCh38.p7	4:53575677	TGCATCTGGGACCCA[A/C]CCCCTGGGCTGGCTA	84708
rs573429232	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, downstream-variant-500B	LNX1, FIP1L1	GRCh38.p7	4:53460310	ATTAATTCTCTGAGC[A/G]AGCATTTTTAGGGAT	84708
rs573444525	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53573237	TGCCAGGGGCTGGGG[G/T]AAGGTGGAATGGGGA	84708
rs573447926	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53588932	GGTATTGCATGACAA[A/G]GCCAATCACATCCAA	84708
rs573473580	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53471790	AACCACAATGAGATA[C/T]CATCTCACACCAATT	84708
rs573474308	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53479322	GAAACTTTTCTATGT[A/T]AAAAAAAAGTAACCA	84708
rs573483497	snp	C/G	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53515183	TTCCTCACATTAGTG[C/G]CAGAGAAGTGTTGGC	84708
rs573490626	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508570	TTTGGTAATTCCTGC[C/T]TGCTGGTGTTTATTT	84708
rs573497165	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53467433	ATAAAAATCAGAGCG[A/C]CTCTCCTCCTCCAAA	84708
rs573535310	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53617476	CCCAAAGCTGTAAAC[A/T]CAGCTGGGGAAACAC	84708
rs573563493	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53582349	GGCAAGAGGAATGAC[C/T]CGCTTCAAAGAAGCA	84708
rs573583642	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53486864	CACATGGCATCTTTC[C/T]ACTGTTTTGGCATTG	84708
rs573601337	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53486234	ACTTGGTGGTCCTCC[A/G]CTCCTGGCAGAGCAC	84708
rs573605288	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507927	CCACAGTAAGTATTC[C/T]ACAGAGGGCAATCGC	84708
rs573612201	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53549555	ATATTTGTTATTAAA[G/T]AATTATGGTTGTTTT	84708
rs573622921	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53630414	ACCAGCAGAGTTCAG[A/G]CAAGGTGACCTTCTT	84708
rs573634737	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53629930	TACATCAATTCTTCT[C/T]ATTCCTCCAAAACAC	84708
rs573669265	snp	A/G	0.0267878	0.112589	intron-variant	LNX1	GRCh38.p7	4:53567532	GCACTAAGTGCCCAC[A/G]AGAGAAAGCAGGAAA	84708
rs573700163	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53549094	ACCTATGTGATGAAA[C/T]AATATGTGCAAACCC	84708
rs573701606	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53596314	GACCTACAGTTTAGG[A/T]GGAAACACTTCTCTG	84708
rs573724120	snp	A/G	0.0103295	0.0711199	intron-variant	LNX1	GRCh38.p7	4:53570104	TGTGGAAGTCAGTGT[A/G]GCGATTCCTCAGGGA	84708
rs573727993	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53535610	TAAATGTTACTATCA[A/G]TTATAAAAATCATTG	84708
rs573729613	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53542591	GGGAATGCCATAGAG[A/G]ACAGAGGCAAGAGGA	84708
rs573743142	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53563660	CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC	84708
rs573758983	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53637372	AAAATCTAATTAGAA[G/T]CATAGGGGTCCATGG	84708
rs573762578	snp	C/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53529800	CCAGAGACAGCATTT[C/G]CCTGGTTCCTAAATG	84708
rs573796328	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53636857	AACAAATGTGAACAA[A/G]GATACAGGGTCATGT	84708
rs573798159	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53642864	CATGGCATGGAAGCT[C/G]CCACCCTCTGAGGAC	84708
rs573806728	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53471933	AGTCAGTGTGGCGAT[A/T]CCTCAGGGATCTAGA	84708
rs573809692	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53582584	TTAAAAGTTATTCAA[A/G]ATATTTTACTCCCTT	84708
rs573825938	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53624395	ATAAGGGGAAACCCC[C/T]TTCACTTGGTTCTTA	84708
rs573891681	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53464377	CCTAGTTTATTGTAG[A/G]CTAATACTTTATCGT	84708
rs573909897	snp	C/T	0.000399281	0.0141238	intron-variant, synonymous-codon	LNX1, LOC101928879	GRCh38.p7	4:53575736	CTGTGGGGGCCACAG[C/T]TCTGTATTGCATCAT	84708
rs573916385	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	LNX1	GRCh38.p7	4:53652818	AAATCTATATCAGGC[A/G]AATAAGTACTTCTGA	84708
rs573931290	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53467410	ACAGAGCAGAAAAAC[C/T]AGAAACTATAAAAAT	84708
rs573951326	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53477225	TTTACACAAGAATAC[C/T]GCTGAAGGAAGGAAG	84708
rs573964732	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53569840	CAAACAACCCCATCA[A/G]AAAGTGGGCGAAGGA	84708
rs573991424	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53561133	ACAGTAAGGATGTAT[G/T]TCAAAGCACAATTAT	84708
rs573994633	snp	A/C			utr-variant-5-prime, upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53591481	TCCTTGGGCCGCCGG[A/C]GTTGTGACCAGCCTC	84708
rs573999756	snp	C/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460042	TAAGGCATCTGGGTG[C/G]CCTCTATGAAATAAA	84708
rs574001836	snp	A/C	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53568089	GGAACTGGTACCATT[A/C]CTTCTGAAACTATTC	84708
rs574035445	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53476665	AAGATGCTAGTGCCA[C/T]GAATCAGCCCTAGAG	84708
rs574036033	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53589609	CACATTAGATCATGG[A/G]GATTATTATCTCCCA	84708
rs574071790	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53648063	AATGCTGCCATAAAT[A/G]TGGGAGTACAAATAT	84708
rs574073819	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53580441	TCCATGCCAGAGTGA[A/G]GTGAGGGAATCTGTT	84708
rs574100349	in-del	-/CTT	0.00358779	0.0422022	intron-variant	LNX1	GRCh38.p7	4:53474768	AAAGTGCAGACTCTA[-/CTT]CTTCTTTTTTTTTTG	84708
rs574118193	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53528973	ATCACAGAGGAAAGC[A/G]GAATAGCCCAATACA	84708
rs574119249	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53556386	ATGCCAGAACTGTGG[A/G]AGAATACATTTCTGT	84708
rs574139794	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53578448	TGTAGGCAACTGTAA[C/T]ACAATGGTAAGTATT	84708
rs574167434	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507251	AGGTGATCAGATTGC[A/G]TCATCCCTGAAGTCC	84708
rs574183746	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53486773	ATGACTGCTTTTCTC[C/T]GTTGAGATTTGACTC	84708
rs574189586	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53611655	TTACCACTAAAATTG[C/T]AAAACTGCAATTACT	84708
rs574200429	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53602587	ACACCTCCTATAATG[C/G]GCGGTCTGTGAGGGC	84708
rs574212598	snp	C/T	0.00119737	0.0244387	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53601988	ACGTGACTGACTTCT[C/T]CAGTCAGCACCATTG	84708
rs574223581	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53651706	TCTCAACCTCTTTAT[C/T]CATGGGTAAAACTGC	84708
rs574231915	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53492201	AATTCTTAGTAGAAT[C/T]GACAGTGAAGAGCTC	84708
rs574242108	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53642554	AAGTCATATGTGGCA[C/T]GGTTATTCTTTATAT	84708
rs574247870	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53554397	AAACTATTGGCCCTC[A/G]AGGCCAAACCAGGCA	84708
rs574267950	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53648506	TATTCTGGATATTAA[C/T]CCCTTCTCAGATAGA	84708
rs574301281	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53514465	GAGGAGCAAAGTGAC[A/G]TCTCATATGGCGGCA	84708
rs574302460	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	LNX1	GRCh38.p7	4:53653510	GGTACTTGTGGCTGC[C/T]TAATCACAGGTGGTG	84708
rs574344086	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53609336	TGTTTTAAAATATAT[C/T]ACTTTAAAAATTTAA	84708
rs574355559	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53625018	TGTTTTAAAAAGATT[C/T]ATATATTTGTGATAG	84708
rs574375482	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53474173	TGGCAGTGGATACAA[C/T]GATGGTGCAGTGCCT	84708
rs574382551	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53558310	TACATTTACATCACC[A/G]GCTGGGAGCAGACAG	84708
rs574418263	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53520917	CAGTGAGCCAAGATC[A/G]TACCACTGCACTCCA	84708
rs574419311	snp	A/C	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53619502	TTTTCAAGTTTCATG[A/C]GTGTTGGGTCATGCT	84708
rs574445811	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53510164	GATTGCCTATTTCAT[A/G]CCAAGCAACACAACC	84708
rs574445857	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53638009	GATTTATCACTGATA[C/G]ATGGCAGCCACGATG	84708
rs574469711	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53624070	AGAGCTGGGCCCTCC[A/C]TGACTCCTTTTCTTG	84708
rs574519603	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53612512	GCTGAATAAATTATG[C/G]CATATCCATATGATG	84708
rs574528504	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53645893	ATTGATTACTATTTC[A/G]TACTGATTACTATTT	84708
rs574533207	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53592479	TCTCCCATCATCCCA[C/T]TGAAACGCTGCGTAT	84708
rs574561415	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53600168	TTCCTCACATCAATC[C/T]TCCACGCACTTGCTG	84708
rs574575019	snp	C/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53481286	ATTATCTTCCTGGGC[C/G]CTTCGGCAAACACAA	84708
rs574585243	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53480574	GCAAAAAGACATCAC[A/G]GAGTCCTTATCCATA	84708
rs574587751	snp	C/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53488736	TAGGACAAATTATAG[C/G]AGAGCAGCCCACCCC	84708
rs574592681	snp	G/T			upstream-variant-2KB	LNX1	GRCh38.p7	4:53653280	GCTTTTCTGAGTTTT[G/T]CTTTTCCCACTGGTT	84708
rs574608321	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53622381	TGCATTTTAATGTCC[C/G]GGTGTCGCAGGAGTG	84708
rs574629050	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53645490	ACTCAAGCCCAAAGA[A/G]CAAGGGCCACTGAAA	84708
rs574632619	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53598947	CAATAAGGAAGCAGA[A/G]CTAAGGACAAACAAT	84708
rs574666185	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53551492	GGCAGAGTTTAACTG[A/G]TATATGAATCCTCAA	84708
rs574678960	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53538081	TTGGTTTCAACCAAC[C/G]ATTGGCTAGATATGT	84708
rs574678976	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53530802	AAGTATTTCAGGGTC[A/T]AATTACATAGTGTCT	84708
rs574697950	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53644411	TATCTCAAAACAAAA[C/T]GAACAAACAAAAACA	84708
rs574722538	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53531876	TCACAACAACATCCT[A/G]GCAATATATTTATTT	84708
rs574724255	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53597966	ATGCTCTTTGCCCAT[A/G]TTCTGAATCCTGGCA	84708
rs574730931	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53502202	TTTCCAACACACAGT[C/T]AGCATCCCAACATCC	84708
rs574742182	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53606155	CAACACATCCAGAAG[C/T]TTCTTTTTTGAAAGA	84708
rs574765056	snp	A/C	0.000798403	0.0199641	nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53604823	GGGAAGACAGGTCAC[A/C]GGCCACCTTTCTCAA	84708
rs574772841	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53631906	GACTCGGTGTAATTC[C/T]ATAGTTGTTAGATGT	84708
rs574809719	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53550263	GAACTGAAATGCTTC[A/G]AGAGTCATTGAGCCC	84708
rs574813479	snp	A/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53468435	AGAAACTGCATCAAC[A/T]AATGAGCAAGCTAAC	84708
rs574816512	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53543616	TTTTTTTTTTCAGAA[A/C]ATTAATTTACTTTCA	84708
rs574847423	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53472419	GTGCAGCACACCAGC[A/G]TGGCACATGTATACA	84708
rs574866870	snp	C/T	0.00279162	0.0372561	intron-variant	LNX1	GRCh38.p7	4:53643954	GCTGTGTTCTCTAGC[C/T]ACTCAGCCACAGTTG	84708
rs574892584	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53501985	CTCCCAGGTGTGTTC[A/G]CTACCCCCAAATCAA	84708
rs574895616	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53503861	TCTGTTGGCTGAGTG[C/T]GGTGGCTCACACCTG	84708
rs574952039	snp	C/T	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53542955	TTCTCACTTGCTACT[C/T]AGGAATCCTGTGCTG	84708
rs574972187	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53582124	CTGTGGTTTGGATGC[A/G]GCTCTGCTACCAACT	84708
rs574983120	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53556432	AACTTGGGTTAATTC[A/G]TGACAGCAGCCCTAG	84708
rs574994419	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53544303	AGGTCAGGCAATATT[C/T]GTGCCTCAGCCTCCT	84708
rs575007718	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53475659	TTCACACATTGGAAC[A/G]GCAAGATAATCATCT	84708
rs575008436	in-del	-/ATCA	0.00318978	0.0398085	intron-variant, utr-variant-3-prime, downstream-variant-500B	LNX1, FIP1L1	GRCh38.p7	4:53459875	TTAAAACTAGTCTTT[-/ATCA]ATCATTACTGCTGTG	84708
rs575010867	snp	C/T	0.00279162	0.0372561	intron-variant	LNX1	GRCh38.p7	4:53544229	TGAGACAGTCTCACT[C/T]TGTTGCCCAGGCTGG	84708
rs575012407	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53495606	AGAGTGCAGTGGCAC[A/G]ATCTCAGCTCACTGC	84708
rs575016830	in-del	-/TCTT	0.00159617	0.0282053	utr-variant-3-prime, downstream-variant-500B	LNX1, FIP1L1	GRCh38.p7	4:53460393	AATAAATTACTAGGA[-/TCTT]TCTTTTAAATAGTGA	84708
rs575050698	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53488272	AACTTAAATTTGCCA[C/T]CCTATTGCCTGCCTA	84708
rs575051377	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53550845	ACACAGCCTTCACCT[A/G]GAGAAGGGGATACTG	84708
rs575058742	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53584919	TTTGCTTACTCAAAA[C/T]ATGACACACACATCC	84708
rs575067075	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53483798	TAGGGGAGAAAGGTC[A/G]TGAAATGAGGGCATT	84708
rs575101254	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53480414	TACCTTCTCCATAAT[C/T]TGATGACTTAGAATA	84708
rs575120143	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53494870	GACACAAAACTATCA[A/G]AACATTATACCGGGT	84708
rs575163522	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53563188	GCGACAGAGTGAGAT[G/T]CCAACTCAAAATAAA	84708
rs575174680	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53530775	AGCCAGTTAAAACTA[A/T]AATTTTTGTTTAAGT	84708
rs575180196	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53563559	TTTTTTTTTGAGACA[C/G]AGTCTCGCTCTGTCA	84708
rs575183586	snp	C/G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53563002	ACGAGGTCAGGAGAT[C/G/T]GAGACCATTCTGGCT	84708
rs575184574	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53571528	CCAAGGAAGACAGGC[A/C]GCACTAGAAGCTGGA	84708
rs575194305	snp	A/C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53649840	ACAGTGGACTGGGAG[A/C/T]TCCTTGAGGGTGGTG	84708
rs575203672	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53537361	ATTGACAATGTTTTG[C/T]CTGAGGGTCAAGTTC	84708
rs575230949	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53515796	CACATGCTTTCACTT[C/T]TAAAGAATCTGGATG	84708
rs575245501	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53637762	TAAAATGTAAAAGAA[A/G]GAGTGTCTTAGAATT	84708
rs575255062	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53631838	TAATCAATTCAGAGT[C/T]TCTTTGGAGGTGGAG	84708
rs575265931	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53516631	AGGTGCATGGCAGGT[A/G]CCAGGAATGGTAGAT	84708
rs575269126	snp	C/T	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53529929	TTAACATGGGGCCTG[C/T]GGACAAAAATGCTAC	84708
rs575284871	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53479465	ACCACAAATATGGCA[C/T]GTGTGCATGTGTCCT	84708
rs575293402	snp	C/T	0.0023933	0.0345097	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53522690	CAAATAGGAATTGCT[C/T]TTTTTCTGATTTCAA	84708
rs575301060	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53521515	TCGGGGTTTGGAAAC[A/G]TGTCATGCAAAGATA	84708
rs575337754	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53618658	GAGGGCCTTGAAGGC[A/G]GTGCTGGCCAATAGG	84708
rs575339187	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53510878	GGGAGGACACAGCAT[A/G]TCCTAGTAAAAGAAA	84708
rs575344075	in-del	-/TGA			intron-variant	LNX1	GRCh38.p7	4:53464974	AATCTGTAAGATGTT[-/TGA]TGATAACTTTTGCAG	84708
rs575347909	in-del	-/A			intron-variant	LNX1	GRCh38.p7	4:53489893	GTGTACTGATCTGTT[-/A]AAAAAAAAAATACAG	84708
rs575415560	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53535609	GTAAATGTTACTATC[A/G]ATTATAAAAATCATT	84708
rs575423293	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53624488	CTCCCCAGCCACATG[A/C]AACTGTGAGTCCATT	84708
rs575431433	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53487411	TAGGTATATGCTTAA[G/T]TAAAATGTATGATAA	84708
rs575442126	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53650604	ATAGATACGTAAATA[C/G]AGGAGGAAGCTGGGA	84708
rs575462097	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53644995	ACCTAACTCCTCAAT[C/T]CTTGCCAACAGCAGG	84708
rs575478620	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53543428	TTGATAAGTATTTGT[C/T]ATTAAATTATACTCT	84708
rs575490683	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53474084	AGGAATGAAGTGATA[A/C]AATAATTTGATATCC	84708
rs575493158	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53550179	TGAATGAGGGCCATG[C/T]GGCTTCAATTTCCTT	84708
rs575525445	snp	A/T	0.000399281	0.0141238	nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53604125	TAGTGGGATGGAGGG[A/T]GATTTAATCAAATTG	84708
rs575579606	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53516677	TCCTATGTGACACCA[A/G]TGAGGAAAGAACAGA	84708
rs575591263	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508599	TTTGACCATGAAAGC[A/C]CTTAGTCACACCCTC	84708
rs575607506	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53474122	CTGGCGCATGGCTGT[C/T]TAGATGTACCATAAC	84708
rs575627448	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53512927	TCCCTGAGCACTCGG[A/G]TGAGTTTGGGCCTCA	84708
rs575630034	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53555834	TAGATTGCTTGTGTC[C/T]GTTCAGTTATTCAGC	84708
rs575644476	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53610282	ACAAAAAGTTGACTA[C/T]TTGAAAATTTAAAAA	84708
rs575689898	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53596527	TCTTATGACAATTAC[A/T]CATATTTTTATGTTT	84708
rs575692958	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53561578	TTTGTAGACAGCTAG[C/T]TGTGTTGTCCTGAAC	84708
rs575777432	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53536836	GTTATTTAAATAACA[C/T]AAAAGACATGGTAGA	84708
rs575789410	snp	G/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53595371	TCAAGGGCTAACTGC[G/T]TCATGTCCTCACATG	84708
rs575795898	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53638588	GACTACTTAGTGCCC[C/T]GTTTTTCCTCATTTT	84708
rs575801923	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53618057	TATAGTTTTTATAAT[C/T]AAAAGATACTGTGAT	84708
rs575803402	snp	A/C	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53471872	GGAGAAATAGAAACA[A/C]TTTTACACTGTTGGT	84708
rs575815269	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53540927	GGATCACTTGAGGTC[A/G]GGAGCTCAAGACTAG	84708
rs575849393	snp	C/T			upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53593210	CACAAAGGCCCCCCT[C/T]TTCACGCGGACAGGG	84708
rs575864166	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53494782	GAAGTGAATGAATGG[G/T]TTAGAACATAAGAGC	84708
rs575871303	snp	C/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53556277	CACCTGCAGCACCCC[C/G]CTCCACAAAACTAGA	84708
rs575872895	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53635767	CACTCCCAGGTTTTA[A/G]CCTAGTGCTTTTAAT	84708
rs575876910	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53540308	GGATGGCTTGAGCCC[A/G]AGTGGTTGAGGCTGC	84708
rs575913990	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53590067	AGTAAGAGACAAGTG[A/G]TGGCCAAACCCCCCC	84708
rs575923851	snp	A/T	1.66651e-05	0.00288657	synonymous-codon, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461560	TCCAGCTGTGTTTCT[A/T]CGTAATACAATATCT	84708
rs575946008	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53641351	GAAAGTGAGAGGGTG[A/C]CACAGCAGGGCTTTC	84708
rs575949730	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53546644	GGATTAGACTAAATC[A/T]TCTCCAAGCTCTCCT	84708
rs575970507	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53600342	GAATGGAGTGGGAAA[A/G]GCAAAAGCCAGAGGA	84708
rs575989778	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53488972	CCCACTGAGCAACGA[C/G]TTGGAGGCTCCAGAA	84708
rs575992295	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53557625	TACCCCAAAAAAGCA[A/G]CACTGACACTGAAGC	84708
rs576008476	snp	G/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53588787	ACCCACTGACCTCAA[G/T]CCACTAATCCCTTAC	84708
rs576015445	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53607192	TGTTTGCAGATGATA[C/T]GATTCTACACCTAGA	84708
rs576019579	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53468909	GACTTTAACACCCCA[C/T]TGTCAACATTAGACA	84708
rs576023377	snp	C/G	0.00438332	0.0466095	intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53559837	AAAAAAAATTAAAAT[C/G]TTTTTCAGAGATGAG	84708
rs576024891	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53649849	TGGGAGTTCCTTGAG[G/T]GTGGTGACTAAGGTT	84708
rs576027547	snp	A/C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53468145	AACAGCTGATCTCTC[A/C/G]GCAGAAACTCTACAA	84708
rs576032604	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53592422	GGGAGGTATCCCAGG[A/T]CTGTTAAACTCTCTG	84708
rs576050346	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53597144	TTTTCTACGAGCCTG[A/G]AGATGAGTGCCTCTA	84708
rs576051446	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53559161	AAAAGTCTACAGGAT[G/T]AGACGAGTTGCAATG	84708
rs576082089	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53651641	AATGGAGACAGGATG[G/T]GCTGCTGGTCACCCA	84708
rs576091248	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53593426	CTTCACCGAACAGCC[C/T]GGAGATCGTGAGGTT	84708
rs576138805	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53534046	CACTGACAGTCACAG[A/C]CTACTTTACGAGTGT	84708
rs576158104	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53464200	CTGTGTTCAGAAAAG[C/T]TTAACTTCCTGGCCC	84708
rs576168191	snp	A/G	0.00199481	0.0315187	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53599327	ATGTGAGTAACCTCT[A/G]GTCGTCCTCACTGCT	84708
rs576170489	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53591814	AGGCCCTCCCCTTTC[C/T]CCATATCTGCCCACA	84708
rs576214565	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53564812	CCAGCCGAAGCAGGG[C/T]GAGGCATTGCCTCAC	84708
rs576229497	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53484297	AACTAGGACCTTGTT[C/T]TAAAAATCTCAAGTA	84708
rs576264266	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53482613	CAGAGGAATGGAAAA[C/T]CAAATACTGCATGTT	84708
rs576266360	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53613159	GGAAGAGAAGAGGAA[C/G]CACCAAGCCAAAAAA	84708
rs576270079	snp	G/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53587876	CAGGCATTTCCACTG[G/T]CAGCCACTCTACCCT	84708
rs576307537	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53587395	AGGAACAGTGACACA[A/G]TCTTCCTTCCAAACA	84708
rs576318429	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53506268	TGATAGTCCTATCCC[C/T]TTAACATTATTGTCA	84708
rs576325913	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53585499	GAACCTGTGACTATG[A/G]CCTTACAGGAAAACG	84708
rs576342614	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53606366	TGGAAACATACAACC[C/T]CCCAAGATTGAACCA	84708
rs576351722	snp	C/T	8.26317e-05	0.00642721	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507455	TTCTAATAGTGGATC[C/T]CTCAAAGGGCCGTGC	84708
rs576360935	snp	C/G			nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53604447	GTTGGATAAAAAGCA[C/G]AACTGGCAGAGCCTA	84708
rs576378165	snp	A/G	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53489793	AGGAGATTAAAAAAT[A/G]TTCTATAATCAAGTC	84708
rs576396795	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53633323	TGCACTATCCTCTTT[G/T]GTCCCCCATGCACAA	84708
rs576403618	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53504276	TTCGCTACAATCTGC[A/G]TTTGCTGCTTTGCCT	84708
rs576442189	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53552206	TCCTCCAGTGACCCC[A/G]CCTAGCTGTCTTGTT	84708
rs576444941	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53594249	GGGTGCACACTTGAA[A/C]TCATCTTTTGAGAGC	84708
rs576460396	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53632775	AAGAGGAAAAGAGGC[C/T]TCTATGGACAACAGA	84708
rs576467441	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53597318	TGCCTTGCCTGGCCT[G/T]TGAGGCTTTTTATGA	84708
rs576488317	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53538777	GCCATTAGTGTCCAG[C/T]CTCATTATTTTCAAG	84708
rs576526870	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53651246	CAATCCAAGTCCACA[C/T]TTTATGTTGAGCTCG	84708
rs576550103	snp	C/T	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53538383	TAGAACAGCTTTCCC[C/T]GTGAAGTTCTGCTGT	84708
rs576563660	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53545008	CGAAGGTGGAGGGAG[C/T]GGTACCCAGATGCTT	84708
rs576568486	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53525143	TCCCCAAACTACTCA[C/T]GGTGGGCTATAATCC	84708
rs576579789	snp	C/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53495212	TTAATTGATAATTAT[C/G]TCAAAATACGAAGGT	84708
rs576584101	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53639981	AGGTTGCAGTGAGCT[A/G]AGACTGCACCACTGA	84708
rs576625517	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53645417	AAGTTGTCAGTGTGC[A/G]CTACCATTGGGGTTA	84708
rs576633243	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53532422	AGAGGTTGTAGTGAG[A/C]CGAGATAGACTCCAT	84708
rs576639064	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53627264	CTTGGAGGTTCCCTG[C/T]TCACTTAATCTCTTT	84708
rs576652221	snp	C/G	0.000365176	0.0135076	missense	LNX1	GRCh38.p7	4:53481850	TGAACACGTCTTTCA[C/G]TGGCCTGGGCAAGAA	84708
rs576653433	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53546612	TAGGCCTTAGTTTCT[C/T]CATCTATAAAATAGG	84708
rs576663899	snp	A/C	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53573118	ATTTCAAAACATACA[A/C]ACATGAGATGAGCTG	84708
rs576665355	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53626554	CAGCATTTTGAAAAG[A/T]TCACCTGGCTTCAGT	84708
rs576670577	snp	A/G	5.00881e-05	0.00500415	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507284	CTGGAAGCCCAGCCC[A/G]TGTCCATCCAGCCTT	84708
rs576680399	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53564522	CTCTTACTCCTGGGG[A/T]GGGCAGAATAATTAT	84708
rs576714214	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53552956	AAACATCTGAGATGA[A/G]CCTAGCTTGTATCAT	84708
rs576726848	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53558333	GCAGACAGGCTGGGA[G/T]TTAAAATGTGTTGGA	84708
rs576736120	snp	A/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53564796	GTGCGCGCACCCTGC[A/G]CCAGCCGAAGCAGGG	84708
rs576758978	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53628796	AATACTACTCAGCCA[C/T]AAAAAGAAATGAAAT	84708
rs576768956	snp	A/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53598743	TTACATCTTGAGTCA[A/T]CTCTTCGTTTTCTTG	84708
rs576770581	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53597662	CCAGGGCAGATTTCT[A/G]TCTAGGAGGCTGCCA	84708
rs576773395	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53518181	GAGAGGCGTGATGTG[C/T]CTTCAAGGTAGAGTC	84708
rs576773552	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53620183	ATCTATCTGTCATCT[G/T]TCTATTTATCTATCT	84708
rs576779218	snp	A/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53503820	CATCTTCTCCCAATA[A/T]AAGGCTGTATCATCT	84708
rs576830855	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53598719	AGGGAGGGCTTACTC[A/G]TTGTTAAGTTACATC	84708
rs576921937	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53469832	AATAACAGGCTCTGA[A/T]ATTGAGGCAATAATT	84708
rs576932774	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53606330	ACAAGCTAGGAAACC[C/T]AGAGGAAATGGCTAG	84708
rs576944811	snp	A/G	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53469377	GCACTGAATGCTCAC[A/G]AGAGAAAGCAGGAAA	84708
rs576967419	snp	A/T	0.0275645	0.114116	upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53593214	AAGGCCCCCCTCTTC[A/T]CGCGGACAGGGTGTC	84708
rs576998309	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53643733	TGGTAACCTTGGGCA[A/G]CTTGCTAAAGCTCTT	84708
rs577005410	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53474829	TGGAGTGCAGTGGCG[C/T]GATCTCAGCTCACTG	84708
rs577011890	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53634368	CCTGCCTCAGTCTCC[C/T]GAGTAGCTGGGACTA	84708
rs577017621	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53474254	CATAGGAGTGTATAT[A/G]CTACCATTGTGTTTG	84708
rs577048894	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53572257	CACAAATAGACTACC[C/T]TACCCACTCCTCCTT	84708
rs577049915	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53640758	TGATGACTTAGGTCT[G/T]GAGGGCCTTTGAAGG	84708
rs577085099	snp	A/C	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53578277	TGATGGGGATATGTT[A/C]TGAGAGGTGCATTGT	84708
rs577093129	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53633203	ATCACATTAAATTTG[A/G]TGAGAAAATGGATGT	84708
rs577128078	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53632608	GAGGCTGTATCTTTG[C/T]TTGGAATTTTCCCTG	84708
rs577135351	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53505544	GGAGTAAGCCACCAC[A/G]TCTGGCCCAAGTAGT	84708
rs577148484	in-del	-/G	0.0209421	0.100162	intron-variant	LNX1	GRCh38.p7	4:53555018	AGAAAGGAAAATCCA[-/G]GAGGGTCTGTGCATC	84708
rs577153977	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53591689	GCGTCTCTTTGTGGA[C/T]AAATAAATCAGTTAG	84708
rs577170881	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53590893	AGGGCAACAGAATTT[G/T]CCCTGAGGAACAGGT	84708
rs577179677	snp	G/T	0.00318978	0.0398085	intron-variant	LNX1	GRCh38.p7	4:53492481	CAACTTTAACCTAAG[G/T]GTCTCAGGAGGCCTC	84708
rs577179738	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53499789	GGAAGAGGCCTGATT[C/T]ATGATCAAGAAGAGG	84708
rs577226193	snp	A/G	0.0023933	0.0345097	intron-variant	LNX1	GRCh38.p7	4:53470039	CAGAGACACAACAAA[A/G]AAAGAGAATTTGAGA	84708
rs577253659	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53644939	GCTTCTCAGTTTTCA[A/G]CAGAGTGAGGGAGAA	84708
rs577256574	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53648441	CAAGTCATTTGTCCA[C/T]TTGAATTGGGTTGTT	84708
rs577282427	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53468495	TCACACATAACAATA[C/T]TCACCTTAAATGTAA	84708
rs577327443	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53526061	TTGTGTGAAAGACTT[A/T]GCTTAAAGGAAAAGC	84708
rs577337737	in-del	-/AATC	0.00119737	0.0244387	intron-variant, utr-variant-3-prime, downstream-variant-500B	LNX1, FIP1L1	GRCh38.p7	4:53459792	CACAGTTTTTTTGTT[-/AATC]AATCAAACACCACTC	84708
rs577345627	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53473723	GCTTAGTACCTGGGT[A/G]CTGAACTCATCTGTA	84708
rs577356236	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53594987	AAAGTGCTGGGATTA[C/T]AGGTGCGAGCCACTT	84708
rs577358686	snp	G/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53620064	AACGAAACACATTGT[G/T]GCTTTTGTTAAACAA	84708
rs577376909	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53513663	CAAATACAATCCAAC[A/G]TGAAATATTCAGAAT	84708
rs577378947	snp	G/T	0.00199481	0.0315187	intron-variant	LNX1	GRCh38.p7	4:53585393	ATCTCTCCATAAGTA[G/T]TTGGAAGAGCTTGTG	84708
rs577385049	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53606064	AAGAGCAAACCGACA[C/T]ACAGTTAGCAGAAGA	84708
rs577395400	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53521091	TTCAGGACTGACTAG[A/G]AAGTGTTTTTAGAAT	84708
rs577396201	snp	A/C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53619591	GTAAGGGTATACAGC[A/C/G]CATGTTGTTTAGCTG	84708
rs577403614	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53550945	CTTGAAAGCCTGGAA[C/T]GCCCAGCTGGGTTTG	84708
rs577404079	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53538702	TGTGATTGAAAGAGC[C/T]TTCAAACTCACAGGT	84708
rs577405061	snp	G/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53616935	TAGTCATTTATAAAA[G/T]TTCCCTGACTATAAA	84708
rs577417097	snp	A/G	0.00159617	0.0282053	intron-variant	LNX1	GRCh38.p7	4:53557170	TTGCATAAAATGGAC[A/G]TGTGTCATGTAGGAA	84708
rs577431857	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53546454	AGTTTAAAATTTTAA[C/G]CACTAGCTCCAATTT	84708
rs577440447	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53539940	GCATCCATGGCAAAG[A/G]TTGACTTGGCCATGT	84708
rs577441397	snp	C/G	0.00597247	0.0543191	intron-variant	LNX1	GRCh38.p7	4:53623991	CTCAAAAGAATATAG[C/G]TTTTTGTGATGCTGG	84708
rs577445334	in-del	-/T	0.00438332	0.0466095	intron-variant	LNX1	GRCh38.p7	4:53627649	CACAGAGGTGAGTAA[-/T]TTTTCTCCTTTGCAT	84708
rs577446609	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53488855	AGTCATCAGTCATTC[C/T]GGTTGATATGTCAGT	84708
rs577459484	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53528301	TCAACTGCAGCTTCA[A/G]ACTATTAAGTAGAAA	84708
rs577475952	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53586882	ATACTGTGCTGGGTA[G/T]TCAACATGTTTTTTC	84708
rs577478211	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53623552	AGAACAATTCTGATG[C/T]AAACCATAAGTTCTT	84708
rs577479713	snp	A/C	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53544899	AGCAATTGGCAGGGC[A/C]AGGCTCTAACTCTGG	84708
rs577515616	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53584941	CACACATCCCCAAAT[C/T]AAAGACAGCATTGGG	84708
rs577524611	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53578316	TTGGTCCTTGGGTGA[A/C]CATCATAGAGTGCAC	84708
rs577528967	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53588850	AGGGCGAGACCCAGA[A/G]AAGTGACCAGGGCCC	84708
rs577568225	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53588108	TTAACACTCACTGAA[C/T]ATTTAAAATATGCCA	84708
rs577577256	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53517601	GATAATTACGTTCTA[C/T]GTGTCACCTCAACTC	84708
rs577588077	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507805	ATTACACACAGTTTT[A/C]ATGATTGGAGGTACT	84708
rs577594141	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53541197	GAAATGGCAGGAATG[C/T]GTTCTGTGATTTCAG	84708
rs577687492	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53642009	GAGGATTGCTTGAGG[C/T]CAGGAGTTAGAGACC	84708
rs577704119	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507200	AAGTAAAAAATATTG[C/T]ATACCCTTGGGAAGA	84708
rs577704852	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53581042	GCAACTGATGGAGAG[G/T]CAATGGGAGGAAATG	84708
rs577740994	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53580315	TGTTCTCCCCCAGGG[A/C]GAGTAGCCTCGGGTT	84708
rs577787181	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53616227	TATATATTGAGACAT[A/C]TTTTTTACTTTTTTT	84708
rs577796560	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53642521	TAGGGGCCCTTCCCA[C/T]ATACCCTGTACACTC	84708
rs577796772	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53601957	TCTATACCACCAACC[C/G]TCCTCACCCCTGCTC	84708
rs577802718	snp	C/G	0.00119737	0.0244387	intron-variant	LNX1	GRCh38.p7	4:53548333	GGGCAGATTGTCATA[C/G]AACTCTTAGGTATAT	84708
rs577814848	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53554354	GTGTTTGGCCCAACA[C/T]TACGAATTGGTTTGG	84708
rs577821606	snp	C/G	0.000206448	0.0101578	intron-variant, utr-variant-5-prime	LNX1	GRCh38.p7	4:53558009	GGCCACCTTCTGTCA[C/G]CTACAAGGGCCCAAA	84708
rs577822462	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53535567	TGTTAGTGAATACTT[C/T]AAAACTCTGCATTAA	84708
rs577833468	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53630381	CAGCAAAAATTGGAG[G/T]GAAAGGACACACACA	84708
rs577835250	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53648473	TTTGTTGTTGTTGAA[C/T]TGTAGGGGTTCTTTA	84708
rs577863812	snp	C/T	0.000399281	0.0141238	intron-variant, synonymous-codon	LNX1, LOC101928879	GRCh38.p7	4:53575682	CTGGGACCCACCCCC[C/T]GGGCTGGCTAATCAA	84708
rs577879838	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53629781	GGAAAATGTGGAGGC[A/C]AACACCCCTGACTTG	84708
rs577894565	snp	A/G	0.00279162	0.0372561	intron-variant, downstream-variant-500B	LNX1, FIP1L1	GRCh38.p7	4:53463014	GAGGATGTGTGCCCA[A/G]TTTTTTGGAGAAAGG	84708
rs577898583	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53535529	TAAATTATTTTTTAT[A/G]GCTAGATTTTATCAT	84708
rs577904708	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53643173	TTTTCTTTTTTAAGA[C/T]AGGATCTTGCTCTGT	84708
rs577908409	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53477124	ACGGGAGGCTGGGTG[C/G]TCACATAGCAAATGG	84708
rs577912209	snp	C/T	0.00398564	0.0444627	intron-variant	LNX1	GRCh38.p7	4:53470786	CCAACTTACAAGGGA[C/T]GTGAAGGACCTCTTC	84708
rs577924721	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53476539	TGAACGCCAAACAGT[A/G]TTTCCACATCCAGGC	84708
rs577940696	snp	C/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53483788	GTTATTGGGCTAGGG[C/G]AGAAAGGTCATGAAA	84708
rs577945889	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53543416	TGTCATACACATTTG[A/C]TAAGTATTTGTTATT	84708
rs577947950	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53614585	TCACAGGTACCCAGG[A/G]AAATGACCAATTGCT	84708
rs577970574	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53540948	TCAAGACTAGCCTGG[C/T]CAACATGGTGAAACC	84708
rs577990596	snp	C/T	0.000798403	0.0199641	intron-variant, stop-gained	LNX1, LOC101928879	GRCh38.p7	4:53575401	CTAGGAAGTCTCTTG[C/T]GTAGAAAGTCAATAA	84708
rs578003263	snp	A/C	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53533930	GCACGCTAAGGTTTG[A/C]GAACTTCTGCCCATG	84708
rs578012744	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53540251	AGCCAGGCATGGGGG[C/T]GTGCACCTGTAGTCC	84708
rs578018667	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53568112	AACTATTCCAATTGA[C/T]AGAAAAAGAGGGAAT	84708
rs578022105	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53483139	GGGGTGGGTCTTTCC[C/T]ATGCTGTTCTCGAGA	84708
rs578068827	snp	G/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53587313	TTTCCACATTTTATG[G/T]TTTTTTTATGGTTTT	84708
rs578132978	snp	C/T	0.000798403	0.0199641	intron-variant	LNX1	GRCh38.p7	4:53466458	TTCCAACTGAGATAC[C/T]GGGTTCATCTCACTA	84708
rs578137699	snp	C/G	0.00874735	0.0655527	intron-variant	LNX1	GRCh38.p7	4:53608774	ACCACAGAATACTAT[C/G]CAGCCATAAAAAGAA	84708
rs578152511	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53627488	TTCCTACTAATGGTG[A/G]GCTCTTATGTTGAAA	84708
rs578162805	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53615057	TAGTTTTGTCATGAT[A/G]CTTCAAATGAATTAA	84708
rs578187146	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53647777	CCATTCTCCCTTTCC[C/T]TCAGCCCCCGGCAAC	84708
rs578193814	snp	A/T	0.000798403	0.0199641	upstream-variant-2KB	LNX1	GRCh38.p7	4:53652680	CCACACCTTCAGGCC[A/T]TCATTAGGTCTGGAA	84708
rs578196994	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53565429	CCAACAGACCTGCAG[C/T]TGAGGGTCCTGTCTG	84708
rs578206090	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53464718	AAACCATTTTCTACT[A/G]CACTATTAGCAGAAA	84708
rs578234913	in-del	-/T			intron-variant	LNX1	GRCh38.p7	4:53589823	CTCTGAATTCCAGTC[-/T]TTTGTCACTTCTTTT	84708
rs578241114	snp	C/T	0.000399281	0.0141238	intron-variant	LNX1	GRCh38.p7	4:53527422	CTTCTGAGAGTGAGT[C/T]TGCATGAATTCCCCC	84708
rs578241476	snp	A/G	0.000399281	0.0141238	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519842	CTTGCGCAGGTTTGC[A/G]CAGTTTGCATATAGG	84708
rs745307044	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53464663	AGGTTGCTTACTACA[A/G]TAAGTTGACACTGCT	84708
rs745311214	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53649299	GCTATGCATTTTTGT[A/G]TACACTATGTAAAAG	84708
rs745360060	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53625758	GCTGTAGTAAGCCAC[A/G]ACTGCATCACTGCAC	84708
rs745375771	snp	A/G	0.000226856	0.0106478	utr-variant-5-prime, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53574043	GAAACTCAGTCACAC[A/G]ATATTTCCTCAGGAG	84708
rs745398820	in-del	-/AAAAA			intron-variant	LNX1	GRCh38.p7	4:53466157	ACTTTTTGTTTTAAG[-/AAAAA]AAAAATCACATATTA	84708
rs745401631	in-del	-/TTCTGCTGT			intron-variant	LNX1	GRCh38.p7	4:53565225	AAAGACAGCAGTAAC[-/TTCTGCTGT]CTCTGCAGACTTAAG	84708
rs745430010	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53585467	CCTGCAAAAGATATA[G/T]CCATGTCTTAACCCC	84708
rs745456503	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53646691	AAAATTAAAAACACT[A/G]TGCTGGCCAGAAATG	84708
rs745475895	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53547875	AGGCTGATGAATATG[A/G]TTCGGGGGTCCTGGC	84708
rs745475951	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53561151	AAAGCACAATTATTA[A/T]GAGATGCTTAGTCTG	84708
rs745476837	in-del	-/A			intron-variant	LNX1	GRCh38.p7	4:53642224	GCAAAATCCTATCTT[-/A]AAAAAAAAAAAAAAA	84708
rs745494002	snp	A/C/G	3.33841e-05	0.00408548	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507487	GAGGAATAGCGACAG[A/C/G]AGGAACAGTAGTTAT	84708
rs745497021	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53480541	GATCAGTTAAATTTA[A/C]ACATTAAGCATTTAC	84708
rs745501856	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53520205	TCTCACAGCAACCCC[C/T]GCGGGTCCAAACCTT	84708
rs745539651	snp	A/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53595896	CATGACATATTTCTA[A/G]AGTTGTCTATGATGA	84708
rs745578749	in-del	-/A			intron-variant	LNX1	GRCh38.p7	4:53528707	CTGTATAGCCTAGAC[-/A]GCAACTAGTGAGAAC	84708
rs745586626	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53482076	ATGTTGCTCCAAGGG[A/G]AAACTAGGGAAGGTT	84708
rs745607423	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53636624	AGAAGCAGCCTGATA[C/G]ACCCTGGGTTTCTAC	84708
rs745639284	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53491594	ATGGTATCTTGGGGA[C/T]AAATGGCACATGAAA	84708
rs745651431	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53492706	AAGACGCTGAGGTGA[A/G]TCAAAGTTCTTTTTG	84708
rs745652766	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53619206	TTTATGTACTGTAAA[A/G]TTCATGCTTTAAAAC	84708
rs745668899	snp	A/C			intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53559718	TGTGTCACAATTATA[A/C]CTCACTGCAGTGGTG	84708
rs745680183	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53615129	GGAGAAAAATGCCAC[A/G]ATTGAAACAGTAGAA	84708
rs745685512	snp	C/T	3.29468e-05	0.00405861	missense	LNX1	GRCh38.p7	4:53496172	CCCCAGGCTCATCCA[C/T]CTTGCGCACCAGTTT	84708
rs745686956	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53645937	CTTATAAAGCTGATA[C/T]ACTCAATTTCTACTC	84708
rs745694266	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53607341	GCTGAGAGCCAAATT[G/T]AGAATGCAATCTCAT	84708
rs745751439	in-del	-/A			intron-variant	LNX1	GRCh38.p7	4:53537013	TCTACCTTTTTGTTT[-/A]ACTGCTTTTTTATAA	84708
rs745767753	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53472860	TCCAGAGAGTTGTTA[C/T]ATTGTGCTGTGTTGT	84708
rs745791750	in-del	-/TGC	1.88984e-05	0.0030739	intron-variant, cds-indel	LNX1, FIP1L1	GRCh38.p7	4:53461088	AGTATTTTAATTCGT[-/TGC]TGAAGTTAATGCAAG	84708
rs745802030	snp	C/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53513340	CCTCACTTCACAGAT[C/G]AAGATATGGACAGTA	84708
rs745802090	snp	A/G	1.65021e-05	0.00287241	intron-variant	LNX1	GRCh38.p7	4:53476733	CCACGCCCCTACAGG[A/G]ATGTTGTGTTTGGAC	84708
rs745808195	in-del	-/GG	1.64821e-05	0.00287067	frameshift-variant	LNX1	GRCh38.p7	4:53496206	TCCAAGCTGCTCCTC[-/GG]GGCTACTTTTGTTGA	84708
rs745818534	snp	A/G	1.6476e-05	0.00287014	missense	LNX1	GRCh38.p7	4:53476819	GCCATGTTGTGGTTG[A/G]AGTCCAGGGCTGCTG	84708
rs745823704	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53618236	CTTTCACTGATATCT[A/G]GAAATACATGTCAAG	84708
rs745832355	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53542797	TTGCATTTAAATCTG[C/T]ATTCGGAACACGTGA	84708
rs745855504	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53581041	AGCAACTGATGGAGA[A/G]GCAATGGGAGGAAAT	84708
rs745874508	in-del	-/G			intron-variant	LNX1	GRCh38.p7	4:53490931	CATTTTTTTTTAAAA[-/G]GTTTTTCCTGCTTAT	84708
rs745909229	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53483746	GAAGGGGCAGTGACC[A/T]GCCAGCTTTCTTCCT	84708
rs745928075	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53562144	CAAAATGGAAATGTG[A/G]TCTTGAGCCTAAAAT	84708
rs745936962	in-del	-/TCTTGTGGTAGTAAG			intron-variant	LNX1	GRCh38.p7	4:53494186	TTTCCCCCATACCAT[-/TCTTGTGGTAGTAAG]TCTCACAAGATCCAA	84708
rs745993232	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53522386	TAAAGTCTACTAAAT[A/G]TAAGGCACCAGGCTT	84708
rs745993371	in-del	-/AAA			intron-variant	LNX1	GRCh38.p7	4:53554850	AGCGAGACTCTGTCT[-/AAA]CAAAAAAAAAAAAAA	84708
rs745995412	snp	C/T	1.66396e-05	0.00288436	missense	LNX1	GRCh38.p7	4:53481794	CGGCTTCCTGAAAGA[C/T]GTCAGGGCTCCGCTG	84708
rs746012621	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53553975	GCTAAGGAATCCGGG[A/G]GTAGCCAACCCGGAG	84708
rs746038654	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53620867	CATGTGTTCGCCACT[C/T]AGGGAAGGATGAGAA	84708
rs746075157	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53504549	TGTGTTCACTGGAAG[C/T]AGCACTTTTAATTCC	84708
rs746076636	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53476578	TTGCCCTAGAATGTC[C/T]GCATGCATTTTCAGT	84708
rs746091749	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53622001	ATTCTCATATACATT[C/G]GTGCAGAGGCCCCTT	84708
rs746092305	snp	G/T	1.66421e-05	0.00288458	missense, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461477	GTTCCTTCAACAATG[G/T]ATTTGATGAAAAAAG	84708
rs746103143	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53494002	TGCCTCGTCTATGGC[A/T]GCTTTTTAAAATACA	84708
rs746109210	snp	C/T			upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53592591	GCCCAGAGAGAATTT[C/T]TTTTCCCCTTCAGGA	84708
rs746124494	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53533516	CAATTCTCCTTCCTC[A/G]GCCTCCTGAGTAGCT	84708
rs746134132	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53580849	CGTTCCTTTACTTTG[A/T]TAAATCTCATTCCAA	84708
rs746151053	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53647921	CTCAAGTTTCAACCA[C/T]GATGTGGCATGTGCC	84708
rs746174608	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53475245	AATAGCTTTCAAACA[C/G]AAAAAACAAAATAAT	84708
rs746192045	snp	C/T	5.06197e-05	0.00503063	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508276	CTTTGGCTCTGCTGC[C/T]ATTCCTCAGTCAGCC	84708
rs746230898	snp	A/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53603363	TGGGAAGAGAAAGAG[A/G]AAAGGATTGGGGTAA	84708
rs746274443	snp	C/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53516049	TGAAGCCAGGAGTTA[C/G]AGACCCGTAGCAGGA	84708
rs746293684	snp	A/T			utr-variant-5-prime, upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53591466	GGTGAACCGAGCAGC[A/T]CCTTGGGCCGCCGGA	84708
rs746294640	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53538261	TCTGCACCCCTTTCC[A/C]CTGGACTGCCTACAG	84708
rs746312215	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53557250	GTCATGATGGCTACA[A/T]TTTGCTCCAGACCAT	84708
rs746318877	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53626834	TGAGTATTAAGTTTA[C/T]TTTTGAAATCTAATA	84708
rs746336204	snp	A/G	1.75631e-05	0.00296332	missense, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573839	TAGGTGTGTCCACAC[A/G]GAGTGTCCAGGGGGT	84708
rs746347395	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53487371	AAGCCAAATGCATGA[C/T]AACATTTGCTGCCTT	84708
rs746349310	snp	C/T			intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498170	AGGGCCGTAAGACTA[C/T]AGGAAATTGACTTTC	84708
rs746351938	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53627062	GCTTCTGCAGGAGTT[C/T]CTCTTGTCCTCTGCA	84708
rs746385362	in-del	-/GTT			intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53462218	GAAACTGGATAGGAA[-/GTT]GTTATAAAAGGAATG	84708
rs746409231	snp	C/T	1.68516e-05	0.00290268	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498608	TTTTTTATATCAAGC[C/T]CCTTGCTGCAGCCCC	84708
rs746413171	snp	A/C			utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460450	TCACATACTAAAAGA[A/C]AACTATAACTTCTGA	84708
rs746462216	snp	A/C			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53502681	ATTCTCTGTAGAATG[A/C]AATGCTGTTTGATAG	84708
rs746484419	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53488814	TGGAAGCATCAGAAC[C/T]GAATGATATGCTAGA	84708
rs746505760	snp	A/C			splice-acceptor-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53574089	GAGACATCCACACAC[A/C]TAAAAAAGAACAAGA	84708
rs746524220	snp	C/T			intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53575224	TGGCCTCAAGAGATC[C/T]ACCTGCTTTGGCCTC	84708
rs746525372	snp	C/T	2.34365e-05	0.00342311	intron-variant	LNX1	GRCh38.p7	4:53496415	GGCAGGTGGAACAAT[C/T]GTGCGGTCAGCTCCA	84708
rs746534370	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53526256	CCTCATGTTGATATC[A/G]GAAATTCAATTTGAG	84708
rs746537824	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53616416	GGGAAGTCAGCATAT[A/G]TTGACCAGATTATCT	84708
rs746541745	in-del	-/G	1.96965e-05	0.00313813	intron-variant	LNX1	GRCh38.p7	4:53496407	GACCTGGGGGCAGGT[-/G]GAACAATCGTGCGGT	84708
rs746559454	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53642887	CTGAGGACCGTTATG[G/T]TCGCCTGGGTGTAAC	84708
rs746565102	snp	A/T	1.65307e-05	0.0028749	intron-variant	LNX1	GRCh38.p7	4:53476986	CAAAATGTCACCTGA[A/T]GGCCAGAGAAGCAGA	84708
rs746571674	snp	A/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53603525	AGGTTTAATTGCTTC[A/T]TGATTCTGCAGGCTG	84708
rs746579587	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53528223	TGACAGCCAAAATAT[G/T]TAAGAAATACATAGT	84708
rs746606866	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53537585	CACTCTTTCCATCTC[C/T]CCATTTACATTAGTG	84708
rs746608894	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53550380	CTACCTCCTTCCTTC[C/T]AGGTCCTCGTCCAAA	84708
rs746609645	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53638281	ATAGACCTTTCGATA[C/G]TTTAATAATGCAGAA	84708
rs746645573	snp	C/T	1.71316e-05	0.00292669	missense, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573950	AAGGAGTGGGCTTGG[C/T]CACACACTGCACACA	84708
rs746649217	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53464749	AGACAATCTCACGTA[A/G]AAATGTTCAGGAGAA	84708
rs746660775	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53626898	TCTGAAATGGAAATT[A/G]AAGCTAGAAGCATTG	84708
rs746670616	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53585584	TCTGAGTGGGTCCTA[A/T]ATTCAATGACAGATG	84708
rs746696672	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53538557	CTGAATAAGCCCTAC[A/G]ATAGGAAAAGTCAGA	84708
rs746702156	snp	A/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53597810	TTAAAATTTTCTCAA[A/G]CTATCCTGAACCTAG	84708
rs746748455	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53647630	CACATAACATGAAAC[G/T]TGCCATCTTAACAAT	84708
rs746765287	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53637563	GTAGCATTGCTCAAT[C/T]CCCACGACACTGTAA	84708
rs746770337	snp	C/T	1.80536e-05	0.00300441	utr-variant-5-prime, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53574009	CTGGTTCATGATGGA[C/T]TGGAGAGCAGTATAA	84708
rs746770361	snp	C/T	1.64779e-05	0.00287031	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507397	CCGCTCTTTGTCCTT[C/T]GAAGAACACTCAAAG	84708
rs746771663	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53482343	GCAAATATTTGGGCA[C/T]AGGAAAGGTTTAGCA	84708
rs746779661	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53546285	GACCCAGGCTGCACG[C/T]GTTCAAAATTGGTCG	84708
rs746800411	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53561274	CATTCTGTCACCAGA[C/G]TGGAGTGCAATGGGG	84708
rs746828103	snp	A/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53596931	TATTTTCTTATTCAT[A/T]CGGATTTTTCATTCC	84708
rs746850375	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53562017	ACTTCTCTCTTTTAC[C/T]TTTAAAAGGTCATTT	84708
rs746851178	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53521360	GAAAACATTTCCTCC[A/G]TTCCTCAAAGTGCAT	84708
rs746883948	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53531206	CCCCACCCCACTACT[G/T]TGTCTAGCAGGAAGT	84708
rs746905166	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53619416	TGTGAATTTGCCTAT[G/T]TTGGACATTTCATAT	84708
rs746929301	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53631258	CCTGGACTCTTTGGA[C/T]TGAGTAAATTAATTC	84708
rs746931146	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53579784	TGGCTTTATAGAAAA[A/T]GGTTATCAGATGTAG	84708
rs746938533	snp	C/G	1.71908e-05	0.00293174	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461611	GAAATAGAATGTAAT[C/G]AGTGTACATGCATAT	84708
rs746939882	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53503138	AGTTACTTTTCTCCA[C/T]TGAAGTCTTGAACCC	84708
rs746953736	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53492789	TAGGGGAGAGCACGT[C/T]GGGCAAGGGGTGGAA	84708
rs746975454	snp	A/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53600533	ATTAAAGAATACAAG[A/G]AAGAGAATATCATGA	84708
rs746975516	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53520426	ACAGTCCACATGCCA[A/G]GTCAATTCTTCAGAG	84708
rs746977919	in-del	-/T			upstream-variant-2KB	LNX1	GRCh38.p7	4:53653792	TCACACTTCTGACTC[-/T]TTTTGGTTCTACCCC	84708
rs746987088	snp	C/T	1.64727e-05	0.00286986	missense	LNX1	GRCh38.p7	4:53496142	CACCGCCATCCAGCA[C/T]ATTGAAGATGAAAAC	84708
rs746996966	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53532360	ACGCACTGTAGCCCC[A/G]GCTACTCGGGAGGCT	84708
rs747014079	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53485874	TCACACCTATGTGAT[A/G]TGTACCAAGAAAGTG	84708
rs747025589	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53646874	TATTATTTCATTATT[C/G]TTCCAATTTAACATG	84708
rs747045406	snp	A/G	2.46679e-05	0.00351189	missense, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573675	ACACCTGGGTGCAGT[A/G]CTCCCTGAATGGGCA	84708
rs747060017	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53640386	CAGAGGAAGGATGGA[A/C]CTCTGTATAAGCTCT	84708
rs747068758	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53466826	TAGGTAAAGAAAGTG[G/T]CCTGGAAGCTCAAAC	84708
rs747080906	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53586024	AGATTGCTACATATT[A/T]AGCAACTCTACCCTA	84708
rs747084120	snp	A/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53599297	CAGCTAAAACCCACC[A/G]AAACCAAGATGGCTA	84708
rs747091004	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53551578	TGCGCACGCTCACCC[C/T]CCAAGTGCCTGAATG	84708
rs747100527	snp	A/G	3.982e-05	0.00446189	missense, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573768	GAACCAGAGGCTTGC[A/G]GTCCATGGGACAGAA	84708
rs747100679	snp	C/T	1.64776e-05	0.00287028	missense, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498736	GGACCAGTGGGGTTT[C/T]GCTACCTCCCACCAG	84708
rs747108307	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53587910	ACTCCAAGAGAAACA[A/G]CACAATCTTTGTTAA	84708
rs747187031	snp	G/T	3.41483e-05	0.00413195	intron-variant	LNX1	GRCh38.p7	4:53481699	CTTGCAGGAGCAGGC[G/T]ACCTGCCCTAGAGGC	84708
rs747199228	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53582966	TCACCCAGCAGGCAT[G/T]TCTGCCTAACTACTG	84708
rs747229435	snp	C/T	1.66596e-05	0.00288609	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498863	AATGGACAAAGAGTG[C/T]TTATTTAAGACACCC	84708
rs747254132	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53524201	AAATTATAGTGAAAG[C/T]TTTCACTAGACCTTG	84708
rs747254228	snp	A/G	1.65072e-05	0.00287286	missense, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460923	TATAAAAAAGTGCCA[A/G]GCCAAGAAACAATAG	84708
rs747304587	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53545422	CCATCTCCATGACAA[C/T]ACAGTAGCGATGCAG	84708
rs747315613	in-del	-/AAT			utr-variant-3-prime, downstream-variant-500B	LNX1, FIP1L1	GRCh38.p7	4:53460358	TCGGTGATGGTAACA[-/AAT]AATAACATGGTATTT	84708
rs747343217	snp	C/T	1.65353e-05	0.00287531	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508147	GCCGTGGCTGTGAGG[C/T]TCGCACAGCCGTCTG	84708
rs747344195	in-del	-/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53594074	GGGGAGGGTAGTTTC[-/T]GATAAAGGATGTCTC	84708
rs747351673	snp	A/G			intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53558287	ACTGGTTCTTGGGAA[A/G]CAGCTGGTACATTTA	84708
rs747395102	snp	C/T			missense, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461519	TTGTATTCTTCATAA[C/T]CTCCTACAATGCAGA	84708
rs747406686	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53529264	CACAATAGCTACCTT[C/T]CCCCAGGCATTAACT	84708
rs747490381	snp	C/T			nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53604681	TCTTGCAACCAAAAA[C/T]GAATTATGAATATCA	84708
rs747504510	snp	C/T			missense	LNX1	GRCh38.p7	4:53478565	CCCTTTACTTTTTAC[C/T]TGTTTTTATTCTTCC	84708
rs747533136	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53632942	ATATCCTATGTACAA[A/G]AATCCTTTTGTAGGT	84708
rs747534933	snp	A/G			upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53591598	AGATAAAGCATTGCT[A/G]AGACCTTAGGGATTG	84708
rs747538473	snp	C/T	1.6654e-05	0.00288561	missense, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461472	CTGGTGTTCCTTCAA[C/T]AATGGATTTGATGAA	84708
rs747540639	snp	A/G	3.33478e-05	0.00408323	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508247	AACAGAACCAGCGGG[A/G]AGGTGAAGAAGAGCT	84708
rs747543746	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53504699	TAAAGTGAGAGACAT[A/G]TGGCTCTTCCTTTCA	84708
rs747562572	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53625072	ATTGTACATACAGAT[A/T]AACTTGAAAGGGATC	84708
rs747571449	snp	C/T	0.00013231	0.0081325	intron-variant	LNX1	GRCh38.p7	4:53476709	TTTAAGAAATGTAAT[C/T]GTTTTCTCCCACGCC	84708
rs747592531	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53557483	GTCTCAATAAAGGGA[C/T]GATGCCTGCTTGCAA	84708
rs747595696	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53648883	TTGTCAGGACAATCA[A/T]GACAATCACTATTGC	84708
rs747644731	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53490225	GTATTTTCAGTTTCT[A/G]CATCAAGTCTGGAAT	84708
rs747660089	snp	A/C			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53605781	CAGCTGAATAATATT[A/C]CATTGTACATATGAA	84708
rs747678543	snp	A/C/G	4.94265e-05	0.00497104	missense	LNX1	GRCh38.p7	4:53496258	TCTCGGGGTCTGTAG[A/C/G]CATCCGGGGCCTGTC	84708
rs747681627	in-del	-/A			intron-variant, utr-variant-3-prime, downstream-variant-500B	LNX1, FIP1L1	GRCh38.p7	4:53459827	AAGAGGCTGCATCAC[-/A]AAAGGCAACAAAGGG	84708
rs747695074	snp	C/T			intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53558415	ATGAAAAGCTGCCCT[C/T]CAGTTTGCTATAGCG	84708
rs747702137	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53529932	ACATGGGGCCTGCGG[A/C]CAAAAATGCTACAGA	84708
rs747708174	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53517064	TCCTGCTTTTCTTGC[C/T]CGCCACTGAATCCTC	84708
rs747738295	snp	A/C			upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53593449	GTGAGGTTTCACTTG[A/C]CATGTTCACATACAC	84708
rs747755451	snp	C/T	3.29462e-05	0.00405857	missense	LNX1	GRCh38.p7	4:53476858	CAGTCTTCCTGGGGC[C/T]CATACTCTTTGACTT	84708
rs747761626	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53489410	ACTTATATGGGGTCA[C/T]ACAGATGTCAGTGAC	84708
rs747802822	snp	C/T	1.65419e-05	0.00287588	synonymous-codon	LNX1	GRCh38.p7	4:53496323	CACAGTCAGCCACAG[C/T]ACCTGGCAGGGCTGC	84708
rs747805199	snp	A/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53500133	TGAGAGCCAGGTCAG[A/T]ACCCAGAGTTCTTGT	84708
rs747832625	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53587631	GGCATTTCGAGTAGT[C/T]AAGATCGTATCCTGG	84708
rs747838951	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53631140	ATGGAGTTAAGGGAT[A/G]CAGCTACTTGGAGAC	84708
rs747863614	in-del	-/A			intron-variant	LNX1	GRCh38.p7	4:53578362	GGTATAGCTGACTAT[-/A]ACACCATATAGATGT	84708
rs747869291	snp	C/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53597963	GTTATGCTCTTTGCC[C/T]ATGTTCTGAATCCTG	84708
rs747893409	snp	C/T			upstream-variant-2KB	LNX1	GRCh38.p7	4:53653882	CAGCTGGCATCTGGT[C/T]AAACAAAAGTAAAAC	84708
rs747893979	snp	G/T	1.80984e-05	0.00300813	missense, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573818	TTGGTGAGGCAGAGG[G/T]TGCAGTAGGTGTGTC	84708
rs747919159	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53466676	GCTTAACAAACAGCA[C/T]ACCAGGAGATTATAT	84708
rs747947624	snp	C/T	1.71366e-05	0.00292712	missense, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573905	TCATCATCCACTTCC[C/T]CTGGATAGCTGTAGA	84708
rs747972504	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53521419	ATCTCCGAGTTTGCC[C/T]AAGCCCCTTCTGGGC	84708
rs747985840	snp	C/G	3.33072e-05	0.00408075	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507293	CAGCCCATGTCCATC[C/G]AGCCTTATGGGGAGT	84708
rs748042986	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53538756	ACAAAGATTCGAAAT[A/G]CAGCAGCCATTAGTG	84708
rs748055226	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53562071	TATTTTTCTTTCATT[C/T]AGGGCCTGACCTATT	84708
rs748055796	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53482468	CTTAAGTGCCCATCA[A/G]CTGATAGGTAGATAA	84708
rs748061531	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53647787	TTTCCCTCAGCCCCC[A/G]GCAACTGCCATTCAA	84708
rs748062520	snp	A/G	1.75342e-05	0.00296087	intron-variant	LNX1	GRCh38.p7	4:53481859	CTTTCACTGGCCTGG[A/G]CAAGAAGACACAGGC	84708
rs748081954	in-del	-/AC			intron-variant	LNX1	GRCh38.p7	4:53606485	ACAAACAAAAAACAA[-/AC]AAAAAAAAAACAGAA	84708
rs748139186	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53610371	CCATGAAAGGTCGAA[C/T]TTTATAACATACTCT	84708
rs748143358	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53522379	TGATTACTAAAGTCT[A/G]CTAAATGTAAGGCAC	84708
rs748149840	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53483515	GACCTATGAAACTCA[A/C]ATAAATAGAGCTCTC	84708
rs748152399	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53554177	GTTCTGTCCAGCTCT[C/T]GCCATTGGACTATAT	84708
rs748171459	snp	C/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53601829	CATGCCAGGGGTCAC[C/T]GCAGGTCACTCTGAA	84708
rs748173314	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53474279	TGTTTGTGTGTATGT[A/G]TGTGTATACATATAA	84708
rs748186546	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53638427	CCCAAACTCAATGCT[C/T]ATGGTGCTTTTGTGG	84708
rs748209540	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53548944	AAACCAAATGCTGCA[C/T]ATCTAAGTGGGAGCT	84708
rs748222431	in-del	-/TTG			intron-variant	LNX1	GRCh38.p7	4:53465026	TCACCTACTTGATAA[-/TTG]TTATCAAGTTACATC	84708
rs748229261	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53542166	AAATTAGTGTATGAG[A/T]TATGCAATTGTCAGC	84708
rs748267890	snp	A/C	3.80684e-05	0.00436265	intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573598	TTGGGGGTGGGACTT[A/C]CCGGCTCGCTGATGG	84708
rs748307949	snp	C/T	2.57563e-05	0.00358852	synonymous-codon, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573664	ACAGCGCTGCAACAC[C/T]TGGGTGCAGTGCTCC	84708
rs748359548	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53486325	CTCCTGAGCTCAAAC[A/G]ACTCTCCCGCCTCAG	84708
rs748369987	in-del	-/TT	1.6549e-05	0.0028765	utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460882	TTTGTGATTTTTCTG[-/TT]TTTTCCTCTGACCCA	84708
rs748371313	snp	A/G			nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53604791	TGTGTTTGGATTGGA[A/G]CTGAGCCTCTTGGGT	84708
rs748382388	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53496646	CTTACCCAAGCCCAC[A/C]TATTTATTCCCAGAA	84708
rs748388390	in-del	-/G	3.35509e-05	0.00409564	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461048	TCACCACATCTAAAA[-/G]AAAAAAACAAAACAA	84708
rs748392876	snp	A/G	1.67223e-05	0.00289151	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498627	TGCTGCAGCCCCACA[A/G]CCACAGTCTCTACCT	84708
rs748397311	snp	C/T	1.64855e-05	0.00287097	missense	LNX1	GRCh38.p7	4:53478709	TTTGGATATTTACCA[C/T]CTTCTCATGACAAGT	84708
rs748400334	snp	C/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53600318	CACACAAAAAAAAGT[C/T]CTAGTAGGGAATGGA	84708
rs748424201	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53495944	TGTGGTAGTGACAGG[A/G]TGCCTGGTTCAGGGG	84708
rs748425626	snp	C/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53513446	CCCCTTATATGGCTT[C/G]CCTGATCCCTAGACT	84708
rs748447315	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53538751	GCTGCACAAAGATTC[A/G]AAATGCAGCAGCCAT	84708
rs748450416	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53583169	TGGCAATTTTATAAA[G/T]GCCAATTGTAAATGA	84708
rs748466100	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53629163	ACAAACAAAAAGTCT[C/T]TTCTTGAGACACTGT	84708
rs748466809	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53480988	CCAAGCCAAAGCTAT[A/C]GGACTCTTAATTTGG	84708
rs748490423	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53535331	TACCGTAGTCATTAT[A/C]TTTCTCCTTGAAATG	84708
rs748520133	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53564847	GAAGCGCAAGGAGTC[A/T]GGGAGTTAGTTCCCT	84708
rs748520136	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53477633	TTGGCCTCATCATTT[C/T]CCACCCAGATGTTTT	84708
rs748520469	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53524378	TGAGACCTGTACTAC[C/T]ATTTCACACATAGCA	84708
rs748543145	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53557526	AATAGAGGCAGCAGA[C/T]CTATGCATACAAATT	84708
rs748558715	snp	C/T	5.1796e-05	0.00508875	intron-variant	LNX1	GRCh38.p7	4:53481681	CTTCCCAAGAAATAG[C/T]CCCTTGCAGGAGCAG	84708
rs748582904	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53612739	ATGGGGTCTCGCTAT[A/G]TTGGGTATGGCAGTG	84708
rs748607930	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53634188	TTTTTATTGTAATTA[G/T]GATTTTCACAAGCCC	84708
rs748609333	snp	C/T			missense	LNX1	GRCh38.p7	4:53476904	CTATCGAGGATGATG[C/T]TCTTTTCAATAATGC	84708
rs748610571	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53623608	GATTTAGTGGTAGCA[A/G]GAGTGTTATGATGGT	84708
rs748629307	in-del	-/A			intron-variant	LNX1	GRCh38.p7	4:53469034	AAATCAACAGAATAT[-/A]ACATTCTTTCCAGCA	84708
rs748644377	in-del	-/ACACACTCTGAC/ACACACTCTT			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519660	CTGTCAAGGTATCTG[-/ACACACTCTGAC/ACACACTCTT]ACACACACACACATG	84708
rs748681667	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53581922	GTCTTTATTTGAATA[A/C]ATTTTGATCTTTTGT	84708
rs748683851	snp	A/G			intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53462034	AAGCAGTTTAAGCCT[A/G]ATCCTAATAAATGAA	84708
rs748689039	snp	A/C			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53506312	TAAAACACTATGTGC[A/C]TGCAGAAAGAGCTCA	84708
rs748696712	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53644718	CCCCAGCACCAGCAG[G/T]GCCTCCTTGCCAGAT	84708
rs748702807	snp	A/G	1.65436e-05	0.00287602	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508130	AAACCTCTGGGGAGG[A/G]AGCCGTGGCTGTGAG	84708
rs748703447	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53495221	AATTATCTCAAAATA[C/T]GAAGGTGAGTTACAA	84708
rs748710539	snp	C/T	1.65295e-05	0.0028748	utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460899	TTTCCTCTGACCCAT[C/T]ATTGATTCTATAAAA	84708
rs748722664	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53544194	GGTGCTGATTTCTCT[C/G]TCTCTCTCTCTTTTT	84708
rs748724963	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53547017	CTTCAGTGAGAGGGA[A/G]GAAGAGACTGTATGG	84708
rs748749624	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53608941	AAGAAGGGAACAACA[G/T]ACATCAAGGCCTATG	84708
rs748762361	snp	C/T			intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53462564	GAAACCAATAAAAAG[C/T]CTTGTGAAATGTTAA	84708
rs748787831	in-del	-/TGTT			intron-variant	LNX1	GRCh38.p7	4:53463389	GCCTTCTTTTAGTGG[-/TGTT]TGTTTTGAGTATTTA	84708
rs748803185	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53607246	AGCTCACTGATCTGA[A/T]AAACAACTTAGCAAA	84708
rs748806362	in-del	-/CA			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53511138	TTAAGTATTCAGACT[-/CA]CGTGCTTTGTGTAAT	84708
rs748806959	snp	C/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53594826	AAGTGATCCTCCCAC[C/T]TCAGCCTCCCAAGTA	84708
rs748829036	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53530070	AAAATTAAATACTTT[A/C]TCCATCAAAAAGTGT	84708
rs748851486	snp	A/G			intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53558565	CTTGACTGCACTGAC[A/G]TATGAAAGAGATGTG	84708
rs748855277	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53571595	GGAATGCTACCCTGC[C/T]GACACCTCAATGTTA	84708
rs748883115	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53583353	TGGGGTGATGTGTCT[A/G]TGTGTGCATGATGGG	84708
rs748886508	snp	C/T	8.23649e-05	0.00641683	synonymous-codon	LNX1	GRCh38.p7	4:53496179	CTCATCCACCTTGCG[C/T]ACCAGTTTTATTCCA	84708
rs748893756	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53547847	GCTCCCATGGAGGGG[A/G]ATGATGACTGTAAGG	84708
rs748908607	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53578199	AAATACAAGAGACCC[A/G]GGAAATTAGAAAGCT	84708
rs748923681	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53490463	GCACCATATTTGAGG[C/T]TTCTATCTCCATAAG	84708
rs748962908	snp	C/T	1.6549e-05	0.0028765	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508112	AGATGGTGGCAGCTG[C/T]AGAAACCTCTGGGGA	84708
rs748979792	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53650664	ACCGTTCTATACTAC[C/T]GCCCTACATATAGGG	84708
rs749002701	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53506805	AGGTTGCAGTGAGCC[A/G]AGATCATGCCGCCGT	84708
rs749013209	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53628829	TGTCTTTTACAATGA[C/G]TTGGACGAAGCAGGA	84708
rs749016230	snp	A/G	1.64751e-05	0.00287007	stop-gained	LNX1	GRCh38.p7	4:53496247	GAAAGCTGTCATCTC[A/G]GGGTCTGTAGGCATC	84708
rs749044202	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53616836	CATAGGTAAATGGCA[A/G]AGTCTCATCTTTTAG	84708
rs749059967	in-del	-/A			intron-variant	LNX1	GRCh38.p7	4:53528946	GAAGAGGCTACCCAT[-/A]AAAAAAAAGCCATCA	84708
rs749071219	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53500413	ATGCTTCTGTCTTCC[A/G]TAGGTGCTGACAGCT	84708
rs749075696	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53540525	GTCTCTACTGAAAAT[A/G]CAAAAAATTAGCTGG	84708
rs749081530	in-del	-/C	0.000118557	0.00769833	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461056	ATCTAAAAAAAAAAA[-/C]AAAACAAGATATGAT	84708
rs749097924	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53541788	AGGAACACAGATTTA[C/T]AAGTAAAAGAGGCAA	84708
rs749104496	snp	A/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53596187	CACAAACATCAGCTG[A/T]TGTGATAGAATGCCA	84708
rs749124201	snp	C/T	1.64754e-05	0.00287009	synonymous-codon	LNX1	GRCh38.p7	4:53476833	GGAGTCCAGGGCTGC[C/T]GGGCTGCTGCAGTCT	84708
rs749129216	snp	A/G			upstream-variant-2KB	LNX1	GRCh38.p7	4:53654019	GATTTGTTTGGCGAC[A/G]CTTTGGGGGTATTTT	84708
rs749155676	in-del	-/GAGAGAGAGAGA			intron-variant	LNX1	GRCh38.p7	4:53652021	TTGATGTGTGTGTGT[-/GAGAGAGAGAGA]GAGAGAGAGAGAGAG	84708
rs749192091	in-del	-/CA			upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53592181	GTTAGAGTCATACGG[-/CA]GTTACAGTGCACTGC	84708
rs749213451	in-del	-/T			intron-variant	LNX1	GRCh38.p7	4:53493231	CTCGGCCTCCCAAAG[-/T]GCTGGAATTAAAGAT	84708
rs749216168	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53523876	CCTGCTTCCCCTGGC[A/G]GTGATAGAGGATTTG	84708
rs749248669	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53586990	ACAAATCCTCTTTGT[C/T]ATTCATTTATTAATT	84708
rs749250997	snp	C/T			intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53499517	GAGGGCATAAACTCT[C/T]GCTGTTCCATGGTTC	84708
rs749253905	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53627860	TTCTCCTTCTGCATG[A/C]CCCTTTGGGAGATTT	84708
rs749276451	in-del	-/A	3.30431e-05	0.00406454	frameshift-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460910	CATCATTGATTCTAT[-/A]AAAAAAGTGCCAGGC	84708
rs749277853	snp	C/T	1.67284e-05	0.00289205	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507278	GTCCCCCTGGAAGCC[C/T]AGCCCATGTCCATCC	84708
rs749279977	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53615426	CACCCTTGCCCTCTT[A/G]GAAGCTTGAAACTGC	84708
rs749303701	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53632909	ACTCCCCTCCTCCTG[A/G]TTACACTTCCTCAAG	84708
rs749313521	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53620738	AAAATTATATTAAAT[A/G]TATGAAGGAAAAAAA	84708
rs749318557	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53579837	CCACTAGAAGGACAA[C/T]TGGATAAATATAACA	84708
rs749324468	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53493012	GTCTTGCTCTGTCTC[C/T]AGGCTGGAGTGCAGT	84708
rs749347473	in-del	-/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53511346	GCGGGGAAGAGCTGA[-/T]TAGCATTGGCCAGGA	84708
rs749361403	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53646906	GTAAATAAACCACTC[C/G]CACCCCTTTGCCCGG	84708
rs749395934	snp	A/G			intron-variant, downstream-variant-500B	LNX1, LOC101928879	GRCh38.p7	4:53577719	CACACCCCGCCTGCC[A/G]TTATTTCCTTAATGC	84708
rs749426501	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53621878	TCATTTCACCCCCAC[C/T]GGATTTGTTGCCTCA	84708
rs749462739	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53555775	ACACCATCCTGGTAA[C/T]GGTGATTCCTGGCAA	84708
rs749462817	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53542956	TCTCACTTGCTACTC[A/G]GGAATCCTGTGCTGT	84708
rs749466054	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53644440	CAAAACAAACAAAAC[C/T]CCAAAACAAGAAATA	84708
rs749481532	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53630485	TCTACTAGTGCCACT[A/T]TTTTCTTATTTTTGT	84708
rs749491950	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53488465	AATAAGTTCTGGACT[C/T]GCTGTAATAAAGTTG	84708
rs749497674	snp	A/G	1.64914e-05	0.00287149	intron-variant, synonymous-codon	LNX1	GRCh38.p7	4:53557947	GCCAAGGCAAGACCA[A/G]CAACAGAAGCGCCTT	84708
rs749518360	snp	A/C			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53515051	AACTGTGACTCAAGG[A/C]TATTTCACAGAGAGA	84708
rs749536803	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53503453	CATCATTACTCTTGC[A/G]TCTCCATCGAAGTAC	84708
rs749549402	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53589971	AATCAACCATGGTAA[A/G]CCAGAGGCAATGTAA	84708
rs749565892	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53487250	GAGTCCATACAGTGA[C/T]TATGAGGGCCAGTGA	84708
rs749594038	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53475130	TGACAAAAGGTAGAG[G/T]GGAAGAAAGACATTC	84708
rs749610087	snp	C/G			intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53499528	CTCTCGCTGTTCCAT[C/G]GTTCTCTGCATATAT	84708
rs749610781	snp	A/C			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53600462	GCTTCCAAGAAAGGG[A/C]AGGCCCTCAAAAACA	84708
rs749621449	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53475449	CAACTAGTGAAGGCT[C/T]AAAAAGGAATCTAGT	84708
rs749637450	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53651340	TTGGGCACCGGACTT[A/G]CACCACGCCCTGACA	84708
rs749648629	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53613683	ATGGCATATATATGC[C/T]ACATTTTCTTTATCC	84708
rs749663073	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53497652	CACAAGAATCAAAAT[A/G]TTTTGTTATGCAACC	84708
rs749673105	snp	C/T	1.67618e-05	0.00289493	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498621	GCCCCTTGCTGCAGC[C/T]CCACAGCCACAGTCT	84708
rs749703696	snp	C/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53601992	GACTGACTTCTCCAG[C/T]CAGCACCATTGTCCT	84708
rs749732147	in-del	-/T			intron-variant	LNX1	GRCh38.p7	4:53544109	TAGCTGTCATTGGGC[-/T]TTTAAATTCTCTGAA	84708
rs749787232	snp	C/T	1.65231e-05	0.00287424	missense	LNX1	GRCh38.p7	4:53496060	TCTGGGCTGCCATAT[C/T]GAAGATCATGTCCAT	84708
rs749808387	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53612827	GAGTTTGAGGCTGCA[A/G]TGATCTGTGGTCGTA	84708
rs749841250	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53526142	GATAACATACGCCAC[A/G]TTCAGCAGGAAACCT	84708
rs749845120	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53494596	AGCATCATACTTAAT[A/T]TTTTCCATTGCAGCA	84708
rs749857405	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53581307	ATGAAGAGTAGGTAT[A/G]TCAAAACTTAAAACA	84708
rs749906087	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53561845	TCCATTTTTAGAAAA[C/T]AAGAGAGTAGGTGCA	84708
rs749914732	in-del	-/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53517920	GGCTGAATGGCCCTC[-/G]CCCCAGAGGACAGGT	84708
rs749934903	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53484141	TCTTTGACTTCTTGA[C/T]CTCCAGAACTGTGAG	84708
rs749957514	snp	C/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53597534	TCTGTCCCTGGGAGT[C/T]CTTGACTGGTAAAAT	84708
rs749974278	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53465688	AAAAATTCTGATACA[C/T]GTTTAAATTGTACAT	84708
rs749983896	snp	C/T	1.64781e-05	0.00287033	missense, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498786	CTGGGATCTACTCGA[C/T]TGATCTTGATGCTGG	84708
rs750051478	snp	C/T	5.02803e-05	0.00501374	missense	LNX1	GRCh38.p7	4:53481733	ACCTTGGGAGTGTTG[C/T]TCCTCTCCCCTGGCC	84708
rs750055973	in-del	-/G			intron-variant, utr-variant-3-prime	LNX1, LOC101928879	GRCh38.p7	4:53576840	CCAAATAAAGTCGGA[-/G]GTTGTTTGTGCAAAC	84708
rs750079677	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53496572	CTGTTCTCTCCAAGC[A/G]TGGCCTGCAGCACCT	84708
rs750096937	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53532164	TACTATCACAATATA[A/T]TGAGTGTTCCCTTCA	84708
rs750099982	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53616498	TCACAGAATGAATGG[C/T]CTGATTCATTTGGCC	84708
rs750109057	snp	C/T	3.36259e-05	0.00410022	utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460859	ATAGTGTTTCAACTT[C/T]TTAGCCTATTTGTGA	84708
rs750126718	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53474912	GCTGGGACTACAGGC[A/G]TGTGCCACCACGCTT	84708
rs750128396	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53589673	TAACTTGCTCAAGGA[C/T]ATAAATGAAGGAGAT	84708
rs750145214	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53502866	AAACCACTTTATTTG[C/T]TCATCCGTAAGAAAT	84708
rs750150164	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53640935	CGTCGGCAGTCCTTC[C/T]GGGGCCTTCCTCAAT	84708
rs750180775	snp	C/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53602802	GAAACAGAAAGTCTG[C/T]ACATCCATGACATAT	84708
rs750181309	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53494998	AGGGTTAAGGAGGAC[A/G]TGGGGCGGGGAGGGA	84708
rs750192359	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53582593	ATTCAAAATATTTTA[C/G]TCCCTTCAGCCAACC	84708
rs750192420	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53607690	AGCAAAAAGAACAAA[G/T]CTGGAGGCATCATAT	84708
rs750198958	snp	C/T	4.96389e-05	0.00498166	missense, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461011	TTCCTGATGTACTTC[C/T]ACCATTGACAGCAAG	84708
rs750206183	snp	C/T	1.65616e-05	0.00287759	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508100	CTGTCATTAAGGAGA[C/T]GGTGGCAGCTGCAGA	84708
rs750248028	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53638745	GCATCATTCAGGCAT[A/G]AGTTATAGCGCTGTT	84708
rs750261984	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53632046	CCGCTGGTTCTTCTA[A/C]TCCATTGAATCTTGA	84708
rs750266651	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53555089	AGGAATCCAAAGCTC[A/G]GATAAAGGGTGGAGG	84708
rs750268386	in-del	-/G	2.32886e-05	0.00341229	frameshift-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573691	CTCCCTGAATGGGCA[-/G]GTCACCAGTAGCTTG	84708
rs750277649	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53651233	GAATGCTCTCCCTCA[A/G]TCCAAGTCCACACTT	84708
rs750292841	snp	A/C/G	0.000181204	0.00951689	synonymous-codon, missense	LNX1	GRCh38.p7	4:53496242	CACATGAAAGCTGTC[A/C/G]TCTCGGGGTCTGTAG	84708
rs750322053	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53553985	CCGGGAGTAGCCAAC[A/C]CGGAGGGTCATTCCT	84708
rs750322343	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53641513	CCCAGGTGGACCTAA[A/C]GACCATGCCTCTGTT	84708
rs750329032	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53642490	TTGTGATGGGTCCTG[A/C]GGGGCCAGCACCAGC	84708
rs750334783	in-del	-/A			intron-variant	LNX1	GRCh38.p7	4:53607452	AAACATTGCTCAAAG[-/A]AATCAGAGATGACGC	84708
rs750356548	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53497549	CGGGTTCCCCCATCA[A/C]CTCTGGGCCCAGAGA	84708
rs750400934	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53483436	GTCAGGTAGTATGGG[C/G]CATTATTCCAGAATT	84708
rs750408647	snp	C/T			intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461352	AGTATAATAAATACA[C/T]GCCTTATCTCAAATG	84708
rs750413963	snp	A/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53601632	ATGCCATGTGGCTGC[A/G]GGGGTTTGGCAGAAG	84708
rs750417291	snp	C/T	1.6483e-05	0.00287076	missense	LNX1	GRCh38.p7	4:53496282	GCCTGTCCATTGTTC[C/T]TGCTGCGGAACTTCT	84708
rs750425165	snp	C/T	6.58957e-05	0.00573964	missense	LNX1	GRCh38.p7	4:53478657	CTATGTGATGCTCCC[C/T]CTGCGACGGTCATGC	84708
rs750444201	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53541066	CCCTTGAACCTGGGC[A/G]GCAGAGCTTGCAGTG	84708
rs750446169	snp	A/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53594335	CAGTTGTAACTCTCT[A/G]TGACATCTTTTATGG	84708
rs750457281	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53479395	GGCAGCCTTGCCTGC[A/G]GTGAGCAAGAGATGT	84708
rs750479396	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53477130	GGCTGGGTGCTCACA[C/T]AGCAAATGGTAAACA	84708
rs750513978	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53635015	ATTTATTTTTTGTAC[G/T]CAAGAAGTCTCACTA	84708
rs750546300	snp	A/C			intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53462517	GGCTATTTTGTTTAT[A/C]TACCGTACCTTAAAA	84708
rs750553836	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53534726	GGGAGGATGTAAATA[C/T]TTTCACAAGAAATAT	84708
rs750568769	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53547292	CCCTCCATTACTCAT[G/T]ATAAAATCCACAAGT	84708
rs750615181	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53489949	AATTCTTACTGGCTC[C/T]GGGGGACTTGAATGT	84708
rs750675072	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53477864	TAAATCTCTTAAGAT[A/G]CCATCCCCCTGTGGC	84708
rs750677564	snp	C/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53517931	CCTCGCCCCAGAGGA[C/G]AGGTGGATTTCTGAC	84708
rs750677984	snp	C/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53605464	TACCTAAATATGTTC[C/G]CAGTAAATTTCCAGT	84708
rs750699197	in-del	-/TAA			intron-variant	LNX1	GRCh38.p7	4:53463777	TCCACTGAAATGAGT[-/TAA]TAAGTATGCTGAAGT	84708
rs750707417	in-del	-/TT	1.65165e-05	0.00287367	frameshift-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460963	TCTTCCTTTAAGTTC[-/TT]TTTCAGCAGTCTTGC	84708
rs750711228	snp	A/G	3.46159e-05	0.00416014	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507963	AAGGAGCCCATTCCC[A/G]GACAACCACCCATTT	84708
rs750726527	in-del	-/AT			intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461957	ACACTTATGGATGTC[-/AT]ATTTTTATTTACTTG	84708
rs750741351	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53489330	CTATAGCTCCATGTT[A/C]ATCCTTATGTTCCCA	84708
rs750746200	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53628212	GAGAAACAGACAACC[C/T]ACAGAATAGGAGAAA	84708
rs750764291	snp	A/G	3.34549e-05	0.00408978	missense, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461570	TTTCTTCGTAATACA[A/G]TATCTTTACAGTTAT	84708
rs750767067	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53497313	TTGAGGAAAGAGGCC[A/C]CATGGAGGAGAAATA	84708
rs750767451	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53587372	TAATGATTAAATCAT[A/G]TTAACCCAGGAACAG	84708
rs750794130	in-del	-/ATA			intron-variant	LNX1	GRCh38.p7	4:53570660	CCTAAAACTTAAAGT[-/ATA]ATAATAAATAAATAA	84708
rs750811443	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53632569	TTCATGTTCCCTGTC[A/G]GATCAGGCTAAAGCT	84708
rs750812637	in-del	-/AGAGAT			intron-variant	LNX1	GRCh38.p7	4:53652031	GTGTGAGAGAGAGAG[-/AGAGAT]AGAGAGAGAGAGAGA	84708
rs750820498	snp	C/T			intron-variant, missense	LNX1, LOC101928879	GRCh38.p7	4:53575681	TCTGGGACCCACCCC[C/T]TGGGCTGGCTAATCA	84708
rs750826895	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53610474	GCACTTTGGGAGGCC[A/G]AGGTGGGCGGATCAC	84708
rs750883256	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53510860	ACAAGCCATGGCTTT[A/G]TTGGGAGGACACAGC	84708
rs750939239	snp	G/T			upstream-variant-2KB	LNX1	GRCh38.p7	4:53652764	GTCCTATAATCCTTG[G/T]CATCTTTTATTTTTG	84708
rs750950470	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53627466	TCTCACATTATTTCA[A/G]TGAGAATTCCTACTA	84708
rs750977689	snp	A/G	2.8366e-05	0.00376592	synonymous-codon, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573643	TTGAAAGTGATGCTC[A/G]AGGTCACAGCGCTGC	84708
rs750992772	snp	C/T			utr-variant-5-prime	LNX1	GRCh38.p7	4:53652419	AGCTATGGGGAGCTT[C/T]GAGGGAGAGTGGTCC	84708
rs751005523	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53466505	GCAGGACAGTGGGTG[C/T]AGCACACCGAGCACG	84708
rs751032595	snp	A/C	1.7704e-05	0.00297518	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461638	ATATTTAAGTTTCAC[A/C]GTTAAGGGAATACTT	84708
rs751046332	in-del	-/C			intron-variant	LNX1	GRCh38.p7	4:53616408	TGATTGGTGGGAAGT[-/C]AGCATATGTTGACCA	84708
rs751078488	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53511613	TTATCAAAGTGAGTA[A/G]AGGTAAATCTGTCTT	84708
rs751084286	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53552185	ACCAGTTTCCAGGAC[A/T]TGTCGTCCTCCAGTG	84708
rs751104118	snp	C/T	1.6906e-05	0.00290736	intron-variant, utr-variant-5-prime	LNX1	GRCh38.p7	4:53557997	TGCCTTCTCCCTGGC[C/T]ACCTTCTGTCAGCTA	84708
rs751126026	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53540024	TTGCTCGGGCTACTA[A/G]TCAATACCAAATCTA	84708
rs751174747	in-del	-/A			intron-variant	LNX1	GRCh38.p7	4:53472793	ATATAGAGGCCAAGC[-/A]AGGGGGAAGGCTGAT	84708
rs751176273	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53649469	GGATTTGAACTCCGG[A/C]AGTCTGGCTCCAGAG	84708
rs751181118	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53494753	CAGCAGAACTTAACA[A/G]ATATTTGCTGGATGA	84708
rs751193726	in-del	-/AACAAC			intron-variant	LNX1	GRCh38.p7	4:53583939	CCCCCTGCAAACAAC[-/AACAAC]AACAACAACAACAAC	84708
rs751218347	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53534457	GCCTGGGCAACATAG[A/C]AAGACCTTGTCTCTA	84708
rs751242446	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53611411	CAAATTGATTATGTG[G/T]GTGGTGTGTTTTACT	84708
rs751260018	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53580657	TTAAAAACAAAAGCA[A/G]TGGCTATGAATGAAG	84708
rs751268827	snp	A/G	1.64762e-05	0.00287016	synonymous-codon	LNX1	GRCh38.p7	4:53478674	TGCGACGGTCATGCC[A/G]AGAGATTCACCGGGG	84708
rs751272906	snp	A/C			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53523406	ATTCTCCTGCCTCAG[A/C]CTCCTGAGTAGTTGG	84708
rs751283882	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53484197	CACCTAGGATAGTGT[A/G]TTTTGTTATAGCAGC	84708
rs751303870	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53505571	TAGTAGAGAACTTTA[C/T]ATGGAGTGGAATTGA	84708
rs751329730	snp	C/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53605861	ATAGCTTGGCTATTA[C/T]GAATCATGCTGCAAT	84708
rs751344408	snp	A/C			upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53592463	AGGAGGGCTGTAAAC[A/C]TCTCCCATCATCCCA	84708
rs751365782	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53633450	TGTTTTTCACTTCTT[C/G]TGGCCATGATAAACT	84708
rs751413177	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53643221	AATGGCACGATCATG[G/T]CTCACTGCAGCCTCA	84708
rs751416679	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53546035	TGGTCTCAAACTCCT[A/G]ACCTCAAGTGATCCA	84708
rs751436120	snp	C/T			nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53604293	TATGTTCTCCTTAAG[C/T]TGGATAGAGAATGTT	84708
rs751436893	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53556971	TCTTGCTATTTTTCC[C/T]GTCTGGTTAGGTTCA	84708
rs751452224	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53516323	CAGTAACTAGCATAA[C/T]TATTGTCTAACATCA	84708
rs751468642	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53632198	GTGGCCAGGTCTTTG[G/T]AACTGACATCAGCAC	84708
rs751494229	snp	C/G	5.05838e-05	0.00502885	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508009	CGGTTGCTCCGGCCA[C/G]AGTCCACTGGGCTGA	84708
rs751506106	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53504267	ATCTGCTGCTTCGCT[A/G]CAATCTGCATTTGCT	84708
rs751517607	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53471166	CAATGGAACAGAACG[A/G]AGCCCTCAGAAATAA	84708
rs751549248	snp	C/T	3.31967e-05	0.00407397	synonymous-codon, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508080	GTTGTCTAGGCCAGG[C/T]TCGTCTGTCATTAAG	84708
rs751577049	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53561428	AGATGGGGTTTCACT[C/G]TGTTGGCCATGATGG	84708
rs751599576	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53544921	TAACTCTGGAGTCCC[A/G]CTTGTGATCATAATG	84708
rs751625447	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53463552	TGTTTTTGATCAGTG[A/T]CCTCAGATACTAGGT	84708
rs751641166	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53496531	CCTGTGTCCAATAAC[C/T]GCACCTTCCAACAGC	84708
rs751666963	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519384	TCTCTCCTGTTAATA[A/G]CAGCAGTCATAACAG	84708
rs751667500	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53547393	TGTTATTCCCATTTA[C/T]AGGTGAGAAAAGCTC	84708
rs751738764	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508321	TTGAAGAATGTATAA[C/T]AGGCTTGTTGAACTT	84708
rs751741935	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53646426	ACCCTGCTGTATTCA[C/T]AGCACTTACAATTTC	84708
rs751819317	snp	A/G			intron-variant, utr-variant-3-prime, downstream-variant-500B	LNX1, FIP1L1	GRCh38.p7	4:53462595	ATGATAAAGTTGATC[A/G]TTACATTTGTTACCA	84708
rs751820609	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53485516	CTTTGGTATTAAGTT[C/G]TTGACAGGAATAACA	84708
rs751821402	snp	A/T			intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461942	TATTGGTGAACAAAC[A/T]CACTTATGGATGTCA	84708
rs751872287	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508325	AGAATGTATAATAGG[C/T]TTGTTGAACTTGGAA	84708
rs751872960	in-del	-/AA			intron-variant	LNX1	GRCh38.p7	4:53652055	GAGAGAGAGAGAGAG[-/AA]AGAGAGACAGAGAAA	84708
rs751877942	snp	G/T	1.64757e-05	0.00287012	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507357	ATTTTCCCTGCCCTG[G/T]TCGGCATGGTTGGCA	84708
rs751897153	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53564842	CTTGGGAAGCGCAAG[A/G]AGTCAGGGAGTTAGT	84708
rs751928798	snp	A/G			intron-variant, downstream-variant-500B	LNX1, LOC101928879	GRCh38.p7	4:53577784	CTAGCTTTTAAAAAA[A/G]ACTTGCAAACCACCA	84708
rs751936308	in-del	-/AACAGAA/AACAGAAGTA			intron-variant	LNX1	GRCh38.p7	4:53590514	TATTGGGCTGTCAAG[-/AACAGAA/AACAGAAGTA]ATACAGGCTGTGTGA	84708
rs751943989	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53479711	TTGATGTTTAAAAAC[A/G]TAATTTATGGTAAAA	84708
rs751961822	in-del	-/TT			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519439	CAGTTTTGTTCAGTG[-/TT]TTTTTTTTTTTTTTT	84708
rs751969886	in-del	-/T			intron-variant	LNX1	GRCh38.p7	4:53556565	AGAGAGGAATGAGCC[-/T]TTTCATAATCTCTGC	84708
rs751974055	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53628299	TAAACATATTAGCAA[C/T]ACAAAACAATCCCAT	84708
rs751997056	snp	C/T	5.27431e-05	0.00513505	intron-variant	LNX1	GRCh38.p7	4:53495994	GTCCGGGGTTTCTGA[C/T]TGGGATCCTGGAATG	84708
rs751997758	snp	A/C			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53518536	AACACTTACAGTGCC[A/C]TCACCAGAGACCACA	84708
rs752003543	snp	C/T			upstream-variant-2KB	LNX1	GRCh38.p7	4:53653704	AATCCACCGAGTGAA[C/T]GAGGCAAAATTAGCA	84708
rs752004286	snp	C/T	1.6504e-05	0.00287258	synonymous-codon, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507435	TATTTTTTTAAATGA[C/T]CTGCTTCTAATAGTG	84708
rs752013527	snp	C/T	3.33456e-05	0.0040831	missense, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461561	CCAGCTGTGTTTCTT[C/T]GTAATACAATATCTT	84708
rs752031289	snp	A/G			intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53559166	TCTACAGGATGAGAC[A/G]AGTTGCAATGAACTG	84708
rs752072392	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53618013	TTATTTTTCTTATTG[A/G]TGTTTTTGAAATTTT	84708
rs752081527	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53529880	CACAGTTCTCAAAAA[A/G]CTTCTCTATTCCAAG	84708
rs752128999	in-del	-/CTT	3.32331e-05	0.0040762	cds-indel, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461542	ATGCAGAAGCCCAGA[-/CTT]CTTCCAGCTGTGTTT	84708
rs752167799	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53530459	TACTTAAAGAATACT[A/G]AGATTATATTTTCAT	84708
rs752177365	snp	A/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53501208	TTGTTATATGCTGAC[A/T]TTGAGTTAAGGTATT	84708
rs752193954	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53473288	ACAGCAATGAAAGTG[A/G]CTGCAAAGGAACAGA	84708
rs752202612	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53501567	GGATTACCGGTGTAA[A/G]CCACCATGCCCAGAC	84708
rs752219404	snp	A/G			intron-variant, downstream-variant-500B	LNX1, LOC101928879	GRCh38.p7	4:53577958	TTTACCATGCGCCAG[A/G]CACTGTGCTAGGGGC	84708
rs752222195	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53547818	AGAAAGGAAGGTGAA[A/T]TTGGTACCTCAGAGC	84708
rs752249693	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53617604	AATATTTTTATACAA[A/C]CTTGTTGGTGAAGAG	84708
rs752274036	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53589361	TTCTTTTTCCAAACT[C/G]TTAACATTGCAGTTA	84708
rs752321820	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53553545	GCTGTAAATATAGGG[C/T]CAGAAAGATGAGAAG	84708
rs752322889	snp	A/C	1.66239e-05	0.00288299	missense, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461546	CAGAAGCCCAGACTT[A/C]CAGCTGTGTTTCTTC	84708
rs752339516	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53571653	GACCCTCAAAACTGT[A/G]TGGTAACAAATTTGT	84708
rs752372881	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53495495	ACCTGGACTTAGCCA[C/T]GGAGACTAAGACTTA	84708
rs752397115	snp	G/T	1.64776e-05	0.00287028	intron-variant, missense	LNX1	GRCh38.p7	4:53557897	ATACAGGAAGTGCAG[G/T]TTGCCCACATTGTCA	84708
rs752398505	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53537323	TCCTATGTGTGCAAT[A/C]GCCTTGGGTCCACCC	84708
rs752400850	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53513179	CTGATCCATATTATC[A/G]ATCACGGTCTCTTGC	84708
rs752422303	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53541257	ACCAAGTTAGGATAC[A/C]ATTAGCAACTGAATC	84708
rs752431993	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53611614	AAACCCATCGTATTA[G/T]GTTGGGGCAAAAGTA	84708
rs752444647	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53624026	TCATGTAACCCAAGC[C/T]CTTAACTCCATCCTT	84708
rs752445387	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53645148	TTTCTCCTGGGGCAG[C/G]AGTGTAACCTAAAAA	84708
rs752450046	snp	A/G	1.80595e-05	0.0030049	synonymous-codon	LNX1	GRCh38.p7	4:53496389	GCTGATGTCCATCCC[A/G]TTGACCTGGGGGCAG	84708
rs752450195	snp	G/T	1.6684e-05	0.00288821	intron-variant, utr-variant-5-prime	LNX1	GRCh38.p7	4:53557979	ATTCTCCGAGCAGTG[G/T]GCTGCCTTCTCCCTG	84708
rs752453502	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53535803	TCAATAGATGAATTA[C/T]TTCTCATTCATCTGT	84708
rs752493198	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53582412	GATCACAAAACGACC[A/G]GATCCTGTAAGAGCT	84708
rs752502902	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53533622	TCAGACTGGTCTCAA[A/T]CTCCTGTCCTCGAGT	84708
rs752517035	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53485694	GGCTAATATGCTTGT[C/T]CTGGCTTTAACTCCT	84708
rs752531049	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53623914	CTCAAGTTCTAGGTT[C/T]CGAACCTCTTTTAGC	84708
rs752539522	snp	A/C			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53598948	AATAAGGAAGCAGAG[A/C]TAAGGACAAACAATT	84708
rs752546531	snp	C/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53594196	ATAAATTCATGCATA[C/T]ATTTATGAGAAATCA	84708
rs752557293	in-del	-/AGG			intron-variant, cds-indel	LNX1, FIP1L1	GRCh38.p7	4:53462183	AAGAACAATTCAAAT[-/AGG]AGGAAAAACAAACTG	84708
rs752572765	snp	A/C	0.495955	0.0447904	intron-variant	LNX1	GRCh38.p7	4:53496430	CGTGCGGTCAGCTCC[A/C]CCTGCCACAACCCTT	84708
rs752579862	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53535974	AAGGTCAGTACTTCC[A/G]AGAGGTATTCAGGGA	84708
rs752588156	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53612308	ACCTCTTGCAGGAGC[A/G]GCATGGCACTATCTA	84708
rs752589702	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53622896	TTTCTTTCACAATAT[G/T]ATTTCTCTTAGAAGT	84708
rs752605728	in-del	-/TC			intron-variant	LNX1	GRCh38.p7	4:53544190	AGAGGTGCTGATTTC[-/TC]TCTCTCTCTCTCTCT	84708
rs752610421	in-del	-/T			intron-variant	LNX1	GRCh38.p7	4:53589443	CAACCACATATGATC[-/T]TTATCTTGATAGAGT	84708
rs752640331	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53633517	CTTGTTCCGTGGGCT[A/G]TGGCCAGGGAAGCTG	84708
rs752644722	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53648690	GGGAAGGAGAACTGC[C/T]TCACAGCTCCAACAA	84708
rs752646608	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53556195	GAATTGAAGAGGACA[C/G]TGAGGAGAAGGACAT	84708
rs752658526	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53517652	AATAATAGCTCTTTG[A/G]CCTAAAGACATTAGG	84708
rs752665620	snp	C/T	4.9423e-05	0.00497082	missense	LNX1	GRCh38.p7	4:53478664	ATGCTCCCCCTGCGA[C/T]GGTCATGCCGAGAGA	84708
rs752669074	in-del	-/TGT	3.3e-05	0.00406189	intron-variant	LNX1	GRCh38.p7	4:53476735	ACGCCCCTACAGGGA[-/TGT]TGTGTTTGGACTTAC	84708
rs752697075	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53494882	TCAGAACATTATACC[A/G]GGTGAAAAAAGCCAG	84708
rs752704215	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53572420	GACATAATGAGCGTG[A/G]AAAACATGTGCTAAG	84708
rs752748061	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53573079	AGAGAAATCTGCTCA[C/T]ACACCCTCTCTGGTA	84708
rs752763825	snp	A/C/G			synonymous-codon, missense, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498812	GCTGGTAATTTCACC[A/C/G]TCTGGAATCAGGTGG	84708
rs752776105	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53586220	GACAATCATATTTAA[C/T]GAGGAGTCTGAAAAC	84708
rs752785508	snp	C/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53516334	ATAATTATTGTCTAA[C/G]ATCAAGGCATAATGT	84708
rs752803854	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53652114	TGGGCAGAGGTGAAG[G/T]TTTTTTTTAAATTGT	84708
rs752807038	snp	A/G	9.88419e-05	0.00702931	missense	LNX1	GRCh38.p7	4:53496232	TGTTGAGAATCACAT[A/G]AAAGCTGTCATCTCG	84708
rs752835069	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53585109	AGTTATCCTGTTTTG[G/T]TTTGGAGGACTCAGG	84708
rs752849268	snp	A/G	1.64751e-05	0.00287007	synonymous-codon	LNX1	GRCh38.p7	4:53476803	CCAGTCACTGGGTGG[A/G]GCCATGTTGTGGTTG	84708
rs752854724	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53489056	ATGAGTTTGGTCAGA[A/G]CAAATCTGGTCTGTA	84708
rs752857998	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53527455	ACCCATAATTAGTCT[C/G]TACGAGCCTGGTGCT	84708
rs752858547	snp	C/T	1.64803e-05	0.00287052	missense	LNX1	GRCh38.p7	4:53496279	GGGGCCTGTCCATTG[C/T]TCCTGCTGCGGAACT	84708
rs752881335	snp	C/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53603102	AAAGTTTCTAATAAT[C/T]AGGGAAAGCAGTTTT	84708
rs752882051	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53526841	GGACCTTAATGGTTG[A/C]AACTCTGTCTTAAAA	84708
rs752883873	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53613643	AGACATGATCTAATT[C/G]TTTTTCATGGCTGCA	84708
rs752896894	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53564453	TGAGGAGGAGTGGCT[A/G]GGTTTTCACTTTCTC	84708
rs752899602	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53549557	ATTTGTTATTAAAGA[A/T]TTATGGTTGTTTTTG	84708
rs752949713	in-del	-/TAAT			utr-variant-3-prime, downstream-variant-500B	LNX1, FIP1L1	GRCh38.p7	4:53460292	AACAAAACAAGTTTA[-/TAAT]TAATTAATTCTCTGA	84708
rs752955629	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53505298	TGGAGTCACCCAGGC[C/T]GGAGTGCAGTGACAC	84708
rs752968070	snp	C/G	3.295e-05	0.00405881	synonymous-codon	LNX1	GRCh38.p7	4:53476893	AGCTTTGAGTACTAT[C/G]GAGGATGATGTTCTT	84708
rs752973861	snp	C/G			upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53593344	AACTTGGGAGGGGAT[C/G]ACAGGCTTCGGTTCA	84708
rs752987686	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53538001	TTGCTTCTCTAATTA[G/T]TCTGTCTCATTCTGA	84708
rs753004945	snp	A/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507592	TGGGTGGTAGGATTG[A/T]AGAATTTGCTTACCT	84708
rs753008885	snp	A/C	2.08675e-05	0.00323006	missense, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573736	GACCAGGATGCTGGA[A/C]TTCTTGCAGTGCTGC	84708
rs753017104	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53626581	CAGTGTAGAGAACAG[C/T]TTAGCAGGGCATCAG	84708
rs753026139	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53615959	AATTATTATTGACTA[C/G]AGTCACCCTGTTGTG	84708
rs753026832	snp	A/G	3.44258e-05	0.0041487	missense, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573869	TCCAGCAAAGCCTGC[A/G]GGCAGATGTGGCAGA	84708
rs753035872	snp	A/G	1.67497e-05	0.00289389	missense	LNX1	GRCh38.p7	4:53481812	CAGGGCTCCGCTGCC[A/G]AACCTGGCGGGACAC	84708
rs753045757	snp	A/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53595700	TTTGAATTCCTTTAT[A/G]TATCTTGACAGGGAA	84708
rs753046766	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53608114	AAACAAAAATTGACA[C/T]ATGGGACCTAGTTAA	84708
rs753063914	snp	A/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53596400	ATTATTGAAGTTGGC[A/G]CACATTTTGTGAAAG	84708
rs753068531	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508504	TGCAAATTTATTCAG[A/G]TCACCATGGTGTCTA	84708
rs753080348	snp	C/G	1.6477e-05	0.00287024	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507347	TGTTTTCAGAATTTT[C/G]CCTGCCCTGGTCGGC	84708
rs753111044	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53491359	TGTGTGAAGGTTTTC[A/T]TAAACATAGCATATT	84708
rs753131312	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53471221	TCTTTGACAAACCTG[A/G]CAAAAACAAGCAATG	84708
rs753131561	snp	C/T	1.65045e-05	0.00287263	synonymous-codon, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498836	CAGGTGGTACAACCT[C/T]GGAAAGACTGAAATG	84708
rs753169782	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53548505	CAAGAAGTTGCAAGA[C/T]TATTGCCCTGTGGAG	84708
rs753206869	in-del	-/AAC			intron-variant	LNX1	GRCh38.p7	4:53569823	AATTTACAAGAAAAA[-/AAC]AAACAACCCCATCAA	84708
rs753212983	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53479818	TTTGCTTTGGATATT[C/T]AGAATAAAACATTTT	84708
rs753213418	in-del	-/GAC	6.59924e-05	0.00574385	cds-indel, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508201	TCCTATCTTTGGTCA[-/GAC]GGCCGTAGTGGGAGG	84708
rs753220555	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53502486	GCTGTTTAACGATCA[C/T]CTGAGGCTTCAGCTT	84708
rs753239699	snp	C/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53504086	GTTGCAGTGAGCTGA[C/G]ATCATGCCACTGCAC	84708
rs753257149	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53637886	GCACCTTCTAACTTC[A/G]ACCCAATGGACTCCA	84708
rs753277137	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53468132	AGCCCATCAGACTAA[C/T]AGCTGATCTCTCGGC	84708
rs753279777	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53619690	ATGTGAAAGTTTTCA[C/T]AAGAACCAATGTTTT	84708
rs753295988	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53579464	TCCTAATCCCTGCTT[C/T]CTTTCCTATGATTTT	84708
rs753331687	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53532083	AGAAACAAGGATGAC[A/G]TTATTTCTAAATACA	84708
rs753338600	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53492604	CTGTGCATAGAGTAG[G/T]AGAGAGATGATTAAG	84708
rs753353054	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53487326	CAGCCAAAGGCTTCA[A/C]CTGCTCATTGGCAGA	84708
rs753382157	snp	C/T	1.66944e-05	0.0028891	missense	LNX1	GRCh38.p7	4:53481748	CTCCTCTCCCCTGGC[C/T]CTGGGGACCAGCTGC	84708
rs753409291	snp	C/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53501779	AGCATTGTTGCCTCA[C/G]AAATGCTGTGACGAC	84708
rs753411874	snp	C/T			intron-variant, missense	LNX1, LOC101928879	GRCh38.p7	4:53576152	CCCAGCAGCAGGGGG[C/T]CTGGCTGCCCCATGT	84708
rs753422682	snp	A/C			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53602467	CTTAGGGTCCTGCAG[A/C]ACTCAGTCACTCTGA	84708
rs753426499	snp	A/G/T	5.41805e-05	0.00520455	intron-variant	LNX1	GRCh38.p7	4:53481896	CACTGTCAGTTTCCA[A/G/T]CCACTGCATTCAGCA	84708
rs753433715	snp	C/T	1.68284e-05	0.00290067	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461431	GATTAGTCATTATTA[C/T]TACCTAATTCTTCCA	84708
rs753449416	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53642417	AATGATATCAGGATT[C/T]TGAATTTGAAGCTCA	84708
rs753459676	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53589367	TTCCAAACTGTTAAC[A/T]TTGCAGTTAATTACC	84708
rs753466457	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53476445	GCTGGGTCTCTGCCC[A/C]CTCTGCCTGTCTGTG	84708
rs753472263	snp	A/C	1.6786e-05	0.00289702	missense	LNX1	GRCh38.p7	4:53481816	GCTCCGCTGCCGAAC[A/C]TGGCGGGACACGACG	84708
rs753477885	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53542576	GATGACACTGAGGTG[G/T]GGAATGCCATAGAGG	84708
rs753487497	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53629921	AGACAACAATACATC[A/G]ATTCTTCTCATTCCT	84708
rs753491643	in-del	-/T			intron-variant	LNX1	GRCh38.p7	4:53555855	GTTATTCAGCAAAAA[-/T]GTTGCCTTTGATTTA	84708
rs753505990	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53514472	AAAGTGACGTCTCAT[A/G]TGGCGGCAGGCAAGA	84708
rs753512092	snp	A/C	1.65999e-05	0.00288091	missense, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461031	TTGACAGCAAGAAGA[A/C]TATCACCACATCTAA	84708
rs753513635	snp	A/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53600174	ACATCAATCCTCCAC[A/G]CACTTGCTGTTTTTT	84708
rs753534163	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53513268	TCTTTTTTAATGTAT[C/T]ATGCTTTATGGATGT	84708
rs753542748	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53619057	CACTCGACCTCACTT[C/T]AGTCACATTTCAAGA	84708
rs753553030	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53530839	TGCTTTAAAATGCTC[C/T]AGAAAAAAGGAGGGG	84708
rs753569335	in-del	-/CTC			intron-variant, downstream-variant-500B, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460105	GCATGTGTACACACA[-/CTC]CTCTTCATTGTGGCA	84708
rs753591086	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53526379	ATGTCTGAATTACCA[A/G]CTGATCAAACCACCA	84708
rs753592455	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53502619	TAAAATAAGACAACA[A/G]TGAAGTTTGCCACAT	84708
rs753621317	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53641411	GAGTTTCTCACACTT[C/T]ACTCTAGTAACATTA	84708
rs753624899	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53613476	TTAAGCCTAGTATCC[A/G]TATTTGTTATTTTTC	84708
rs753676776	in-del	-/CAT			intron-variant	LNX1	GRCh38.p7	4:53606686	AATATCTTTGATGAA[-/CAT]CATCAATGCAAAAAT	84708
rs753691243	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53618679	GGCCAATAGGATGAC[A/G]ATGCAAGCCACATAC	84708
rs753693236	in-del	-/AG			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53596468	AGTAGGGAGAAAAAA[-/AG]AACTTCATTGTTACT	84708
rs753714717	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53649896	CACCCTAGCCAAGCA[C/T]CTGGAACCTCGTAAG	84708
rs753744046	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53612515	GAATAAATTATGGCA[C/T]ATCCATATGATGGAA	84708
rs753744467	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53553861	CATATTTAAAGAAGG[A/C]AAGGCCCTGGTATAA	84708
rs753747128	snp	G/T	3.36604e-05	0.00410232	missense	LNX1	GRCh38.p7	4:53496360	AGACGCACAGCGTAG[G/T]TGTGAGGGACATTGC	84708
rs753761132	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53564509	TTCTGTCTCCCCACT[C/G]TTACTCCTGGGGTGG	84708
rs753783520	in-del	-/C			intron-variant	LNX1	GRCh38.p7	4:53490095	CTGTTGTCAAATGTT[-/C]CTTTGATGAAATGAA	84708
rs753783893	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53561333	CCCAGGTTCAAACGA[C/T]TCTCCTGCCTCAGCC	84708
rs753806375	snp	C/T	6.93385e-05	0.00588765	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507962	CAAGGAGCCCATTCC[C/T]GGACAACCACCCATT	84708
rs753807614	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53476361	ATCCCAGGGCTGCCA[C/T]TAGCAGATTAGGCGA	84708
rs753813741	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53647918	ATCCTCAAGTTTCAA[C/G]CATGATGTGGCATGT	84708
rs753821879	snp	C/T	1.66966e-05	0.00288929	intron-variant	LNX1	GRCh38.p7	4:53478552	GTGCCTTTAAAATCC[C/T]TTTACTTTTTACCTG	84708
rs753854142	snp	C/T	1.71625e-05	0.00292933	missense, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573894	GGCAGATGAGGTCAT[C/T]ATCCACTTCCTCTGG	84708
rs753880231	in-del	-/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53595721	GACAGGGAAATCTAA[-/G]GGGGGGAAGGAGGTC	84708
rs753882827	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53609511	TATTTTTATTTATAC[A/G]GAAATTTTATAGCAT	84708
rs753885156	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53489822	TCTATGTGCATTAAA[C/T]TTACCACAAACCATG	84708
rs753904227	in-del	-/ATG			intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461853	ACACATCTACTGGGA[-/ATG]ATGATAATCATATTT	84708
rs753911594	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53516421	AAAAACCTCCATGCC[A/G]CATTATCAGAGAGAC	84708
rs753926594	snp	A/T			nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53605336	TTAAGGTGTATAATG[A/T]GATGTTTTGATGTAT	84708
rs753956142	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53644225	GGCCAGCATGATGAA[A/T]CTCTGTCTCTACTAA	84708
rs753975077	snp	C/T			intron-variant, utr-variant-5-prime	LNX1	GRCh38.p7	4:53557974	CCTTCATTCTCCGAG[C/T]AGTGTGCTGCCTTCT	84708
rs753986790	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53561627	GTAAAGGTCAACAGA[C/T]GATCCAGGTTAGACC	84708
rs753987553	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53477697	TATTTCCATTTTCTA[C/T]TTTTTTATCTTCATC	84708
rs753998864	snp	C/T	3.29451e-05	0.00405851	missense	LNX1	GRCh38.p7	4:53496120	AGCTGACCATGTCGA[C/T]ATGCCACACCGCCAT	84708
rs754003549	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53564045	TCTCCAGAGAGCTGC[A/T]GTGGGCGCCTGTGAA	84708
rs754006996	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53539502	TTCCCAGTAGCTGGG[A/T]CTACAGGCATGTGCC	84708
rs754007921	in-del	-/GT/GTGT			intron-variant	LNX1	GRCh38.p7	4:53625842	CCCAGCAATTCCACC[-/GT/GTGT]CCGTGTGTGTGTGTG	84708
rs754019542	in-del	-/A	1.64972e-05	0.00287199	intron-variant	LNX1	GRCh38.p7	4:53557825	TCGGGTCCCACCCCC[-/A]ACATACTAGGCACAT	84708
rs754062056	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53489121	GAAAAGTGCCTGATA[C/T]ATTATTAAAAAGTTT	84708
rs754083570	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53615830	GATGTTTTGATACAG[A/G]CATGCAATGCGTAAT	84708
rs754086178	in-del	-/C	1.69874e-05	0.00291435	intron-variant	LNX1	GRCh38.p7	4:53478524	TAATTTCTCTTGATT[-/C]TCTGCCACCCCAGTG	84708
rs754098583	snp	G/T			upstream-variant-2KB	LNX1	GRCh38.p7	4:53653310	TTGCTTAAGCACTTC[G/T]GTGGGCTGACAGCTC	84708
rs754110400	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53527157	AACTAAAATATTCAG[C/T]TTTCTGTTCTCAGCA	84708
rs754124074	snp	C/T	1.65302e-05	0.00287486	intron-variant	LNX1	GRCh38.p7	4:53476715	AAATGTAATCGTTTT[C/T]TCCCACGCCCCTACA	84708
rs754149020	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53497912	GGGATGGGATAGAAC[G/T]GTTATCTGAGTGTCA	84708
rs754163404	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53635847	TTTTACAAATGAATA[C/T]AAATATATGAGAGTA	84708
rs754168708	in-del	-/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53598529	TGAGCCACTGCACCT[-/G]GCCCTGACTGTAATT	84708
rs754174714	in-del	-/T			intron-variant	LNX1	GRCh38.p7	4:53493284	AAATGCCTCTTCTAA[-/T]CTCTGGTTTTGTTCC	84708
rs754183022	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53466459	TCCAACTGAGATACT[A/G]GGTTCATCTCACTAG	84708
rs754222898	in-del	-/TCTC			intron-variant	LNX1	GRCh38.p7	4:53528071	GTGTTTTCCAGTCTG[-/TCTC]CTAAAATTCTTTGTA	84708
rs754232206	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53579633	GTGTCTACTGTCAAC[A/G]CACTAGACAGATTTA	84708
rs754239139	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53627368	CATTTGTAAGAAAAG[C/T]GCAGTCAAGTGTTGG	84708
rs754249617	snp	C/T	0.000109093	0.00738475	missense, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573653	TGCTCGAGGTCACAG[C/T]GCTGCAACACCTGGG	84708
rs754260671	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53637232	AGGACTGCCTTGGCC[C/G]CTAAGAAACTTGTGT	84708
rs754271968	snp	A/G	0.000115362	0.00759393	missense, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498697	CGATCACCCCATCAC[A/G]ATAAATGTGTTGGAT	84708
rs754285136	snp	A/C			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53521058	GAAACTGGGCTATGG[A/C]TCAACGGTGCTTTCT	84708
rs754299383	snp	A/C/T	0.000192637	0.00981244	synonymous-codon, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573724	GAGGAGTTTGTTGAC[A/C/T]AGGATGCTGGACTTC	84708
rs754306018	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53538180	GAGGAAAGGAAACAC[A/G]CATGGCTTGAAGGAT	84708
rs754319408	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53647356	GTATAATATTAATCT[C/T]ATTTGTTTTAGGAAG	84708
rs754346342	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53464346	GTGGTGAAGGGACCA[C/T]CTTTCATTTTGTTTT	84708
rs754369262	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53493219	TGATCTGCCTGCCTC[A/G]GCCTCCCAAAGTGCT	84708
rs754372651	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53521851	TGACCCCAGGCTGGA[A/G]TGCAGTGGCATCATC	84708
rs754382226	in-del	-/TTTG			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53523280	AGCTGTACAATTTTT[-/TTTG]TTTGTTTGTTCTGAG	84708
rs754415885	snp	G/T			intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53499336	GCAAATTTTTACATT[G/T]TTTGTGGAGACGGAG	84708
rs754426385	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53489708	GTTTACCAAGTCACA[C/T]ACTTTATCAAGAATG	84708
rs754432571	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53609110	AATAATGCTTCACTC[A/C]TACAACTATCTGATG	84708
rs754436350	in-del	-/AA			intron-variant	LNX1	GRCh38.p7	4:53541146	AACTCAAAAAAAAAA[-/AA]GAAAAAAAAAAAAGA	84708
rs754457552	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53483062	AAACTTCACCTTGAA[C/T]TGTAGCTCCCATAAT	84708
rs754480185	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53540108	ACTCCAAATGACAAC[A/G]TGGTGGCTCACATCT	84708
rs754496849	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53541220	GATTTCAGGATTCTC[C/T]AGTGAGTGGGTGGAG	84708
rs754503232	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53552190	TTTCCAGGACTTGTC[A/G]TCCTCCAGTGACCCC	84708
rs754508636	snp	G/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53511698	GGGGGGATAAGGAAA[G/T]AAAATGAATCTCCTT	84708
rs754510150	snp	A/G/T	6.71021e-05	0.00579199	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461050	CACCACATCTAAAAA[A/G/T]AAAAACAAAACAAGA	84708
rs754511849	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53464083	GTTGGAAAGACGACA[A/G]TGGATGTAGGATGTT	84708
rs754569687	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53628297	CTTAAACATATTAGC[A/C]ATACAAAACAATCCC	84708
rs754572647	snp	A/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53597882	CTGTCTGTGGTTCTC[A/G]TAACAACCAGACTGG	84708
rs754589951	snp	G/T	1.65438e-05	0.00287605	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508120	GCAGCTGCAGAAACC[G/T]CTGGGGAGGGAGCCG	84708
rs754598639	snp	A/C	1.68026e-05	0.00289845	missense, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461437	TCATTATTATTACCT[A/C]ATTCTTCCATCATTG	84708
rs754609790	in-del	-/AAA			intron-variant	LNX1	GRCh38.p7	4:53610716	CCCGTCTCAAAGAGG[-/AAA]AAAAAAAAAAAAAAA	84708
rs754630234	snp	A/G			upstream-variant-2KB	LNX1	GRCh38.p7	4:53653175	CACTCCCATTATATA[A/G]ATAAAGAAACTGAGC	84708
rs754655662	snp	G/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53597775	TCAAAGGTGATATTT[G/T]GGCCTCCAAAATTAT	84708
rs754659513	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53621140	AGCAGAATTTCAGAG[G/T]TCACTCCTGACCTAT	84708
rs754729226	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53627758	GCACATTGAATCAGC[A/T]CCTGCTAACCCTCTA	84708
rs754749908	snp	C/T	1.64912e-05	0.00287147	synonymous-codon	LNX1	GRCh38.p7	4:53496296	CCTGCTGCGGAACTT[C/T]TGTTCACGCATCACA	84708
rs754757074	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53563063	TACAAAAAATTAGCC[A/G]GGCATGGTGGTGGGC	84708
rs754786705	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53533438	GCGTCTCCCTCTGTC[A/G]CCCAGGCTGGAGTGC	84708
rs754800365	snp	A/G	1.71091e-05	0.00292476	synonymous-codon	LNX1	GRCh38.p7	4:53496371	GTAGTTGTGAGGGAC[A/G]TTGCTGATGTCCATC	84708
rs754808312	in-del	-/T			intron-variant	LNX1	GRCh38.p7	4:53494196	CCATTCTTGTGGTAG[-/T]TAAGTCTCACAAGAT	84708
rs754810853	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53581516	GAAAAAGAGGTTTAA[A/T]GGACTCACAGTTCCA	84708
rs754814216	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53494797	GTTAGAACATAAGAG[C/T]CCAGAACAAAGTCTA	84708
rs754815839	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53531310	AAAAGAAAAGGCCAC[C/T]TGTTCTTTTCCTGCA	84708
rs754854738	snp	G/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53504378	TTCTCCTTTAGCTTC[G/T]TCACCTCTCTCAGCC	84708
rs754872755	snp	C/T	1.64803e-05	0.00287052	missense	LNX1	GRCh38.p7	4:53476930	AATGCCACTGCCTCA[C/T]TCCGGCTGACCTCTG	84708
rs754878841	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53632276	CTGGGCTCCCATCCT[A/C]CCTTTTCTCTCACAG	84708
rs754888035	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53641588	TTTAATTTTGTGCAT[C/T]TGATCAATTTTGGCA	84708
rs754896948	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53496911	TAGATGTGATAGTGT[A/G]TGAGTGAGGGTCTGA	84708
rs754898441	snp	C/T	1.71519e-05	0.00292842	missense, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573897	AGATGAGGTCATCAT[C/T]CACTTCCTCTGGATA	84708
rs754910740	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53587480	CAACCACATAAAAGA[C/G]AGTCTATGTAATGTC	84708
rs754924146	snp	A/C			intron-variant, upstream-variant-2KB	LNX1, LNX1-AS2	GRCh38.p7	4:53591162	GCTGGATTAATGATC[A/C]GAGAAACAAAAAGGA	84708
rs754930977	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53585764	CCTGGAGCCTTCAGA[A/G]GAGTGTGGCCCTGCT	84708
rs754971697	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53505860	ATCTGGAAGAAGGAA[C/T]GTGAATGCCAGCTGA	84708
rs754979887	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53544965	CGTCCCCAGTGACAC[C/T]TCAGACCTATGTAGA	84708
rs754995456	snp	C/T	1.67444e-05	0.00289343	missense	LNX1	GRCh38.p7	4:53496040	GAATCAGATGAGCCG[C/T]ACTTTCTGGGCTGCC	84708
rs754999372	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53537192	TAATAAATAAAAAAG[A/G]CAGCTAACTTGCACG	84708
rs755002624	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53621844	TGGTGCCAGCCAGTG[A/G]TAAATTGCTTTGGAC	84708
rs755015911	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53526594	TACTCTGGAAGTAAA[C/T]AGCCCCTATCTCAAT	84708
rs755030922	snp	C/T	5.07661e-05	0.00503791	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508003	CTAGTTCGGTTGCTC[C/T]GGCCAGAGTCCACTG	84708
rs755055988	snp	A/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53513341	CTCACTTCACAGATG[A/T]AGATATGGACAGTAG	84708
rs755071949	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53525528	CTGCCTGGAATTCCA[C/G]CTCTATTTTGACCTC	84708
rs755075523	snp	A/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53600292	AACATAAAGTGACTC[A/G]AGGACACATGCACAC	84708
rs755075608	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53613554	TGCATTGTTCCAATG[C/T]GGTATTTGGTTTTCT	84708
rs755078079	snp	A/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53514445	CAATCATGGCAGAAG[A/T]TGAGGAGGAGCAAAG	84708
rs755086500	snp	C/T	1.6473e-05	0.00286988	synonymous-codon	LNX1	GRCh38.p7	4:53496122	CTGACCATGTCGATA[C/T]GCCACACCGCCATCC	84708
rs755093359	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53636771	CCCAATTAGCTGATT[C/G]CATCCTATGTCCATA	84708
rs755116092	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53646209	GTTTATATTTCCCAT[A/G]ATTTTATGGCAGAGC	84708
rs755144388	in-del	-/AAC			upstream-variant-2KB, nc-transcript-variant, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53593017	GAGTTGAAGGCTTAA[-/AAC]AACAACAACCACCAC	84708
rs755174269	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508356	TTTGATTTGCCTGCC[A/G]CTATATCCTCTCTTC	84708
rs755184266	snp	C/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53595647	AAAGTTGGGCCTGTC[C/T]TAGTTAACCAGCCGG	84708
rs755190964	snp	A/G			intron-variant, downstream-variant-500B	LNX1, FIP1L1	GRCh38.p7	4:53462631	GTTAGTCAATGTGAC[A/G]TGACTTTTTTCATGA	84708
rs755194220	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53495893	ATGTTGGTCTTTCCA[A/T]CCTGACTCCTTGAAA	84708
rs755198295	snp	C/T	1.65277e-05	0.00287464	intron-variant	LNX1	GRCh38.p7	4:53476717	ATGTAATCGTTTTCT[C/T]CCACGCCCCTACAGG	84708
rs755210395	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53561712	CCAGCCAGCCTTCAG[A/C]CACGTATGTCTTGGG	84708
rs755232290	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53613944	GGTGTAAAAGCATTC[C/T]TTTTTCTCCACAACC	84708
rs755236749	snp	A/C	2.60855e-05	0.00361138	synonymous-codon, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573661	GTCACAGCGCTGCAA[A/C]ACCTGGGTGCAGTGC	84708
rs755261769	snp	G/T			intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53560261	TTGGACATGTCAGAT[G/T]GCTTCTGACATTTGA	84708
rs755265343	snp	C/T	3.295e-05	0.00405881	synonymous-codon	LNX1	GRCh38.p7	4:53476800	GGACCAGTCACTGGG[C/T]GGGGCCATGTTGTGG	84708
rs755271429	snp	A/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53594591	AAAGACCATGACACT[A/T]TTCAACTCAGAAGGA	84708
rs755283866	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53496532	CTGTGTCCAATAACC[A/G]CACCTTCCAACAGCG	84708
rs755288124	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53548382	ATGTTTTTGTGCCTG[C/T]TTTATCATGGATGTA	84708
rs755325902	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53502133	GGATATAATAATAAT[C/T]ATTAACTGAGAGTTT	84708
rs755347960	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53606896	GAAAAGGCTTCTGAT[A/G]AAATTCAACATCCCT	84708
rs755371559	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53501373	TTGGCTCAAAGCAGC[C/T]TTGACCTCATGGGCT	84708
rs755383217	snp	G/T			intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461753	CCTTGGTGACCTTTG[G/T]GCTGTTAGCTGGCTT	84708
rs755385273	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53479719	TAAAAACATAATTTA[C/T]GGTAAAATAGTTTAA	84708
rs755403952	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53588574	ATTTTCTAGTGAGGC[A/T]CTACCCAGTCCCCCC	84708
rs755434273	snp	C/T	0.000155668	0.00882097	intron-variant	LNX1	GRCh38.p7	4:53481670	AAACAAGCAGCCTTC[C/T]CAAGAAATAGCCCCT	84708
rs755446317	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53490009	TTGCAGGTATGGCAA[G/T]GCAAATAGTCCATTA	84708
rs755446858	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53633300	CCACCCCCATCCACG[C/T]ATGGTTCTGCACTAT	84708
rs755457415	snp	C/T			intron-variant, downstream-variant-500B	LNX1, LOC101928879	GRCh38.p7	4:53577812	CCAGACTAGATCGTG[C/T]ACAACAGTCCCTTCC	84708
rs755464521	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53547416	AAAAGCTCAGAGAAG[A/G]TAAGTAACCTGCCCA	84708
rs755478461	in-del	-/TAA	1.66785e-05	0.00288773	cds-indel, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461562	AGCTGTGTTTCTTCG[-/TAA]TAATACAATATCTTT	84708
rs755482335	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53617599	CAGTAAATATTTTTA[C/T]ACAACCTTGTTGGTG	84708
rs755502233	in-del	-/T			intron-variant	LNX1	GRCh38.p7	4:53578155	TTTCTTGATTATGGC[-/T]AGTCAGAATCCCAAT	84708
rs755515017	snp	C/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53597453	GGGGTGCACTCCCCT[C/T]ACCCCCATTTCCATA	84708
rs755535102	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53611897	GTAAAGATAGCTGTA[C/T]TTGACTGAAAACAGT	84708
rs755538410	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53579763	AATTCTCCTTTCAAT[G/T]CACCCTGGCTTTATA	84708
rs755620883	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53579386	TAGAGATATATGGAG[A/C]CAAAACCCCCAATCT	84708
rs755630061	snp	G/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53518927	ATACAAATGGCACAG[G/T]CTGGCAAGTGAGTCT	84708
rs755638829	snp	G/T			intron-variant, downstream-variant-500B	LNX1, LOC101928879	GRCh38.p7	4:53578086	AACAAAACAGGCAGG[G/T]GCTGTCTGACTCCAA	84708
rs755655655	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53628546	GAATGTAAAGCACAA[C/T]CTCTATAGAAAACAG	84708
rs755668547	in-del	-/T			intron-variant	LNX1	GRCh38.p7	4:53485906	TACAGCAGAGCTGTC[-/T]ATTCCAGCAAGCAAG	84708
rs755669707	snp	C/T	6.62219e-05	0.00575383	utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460872	TTCTTAGCCTATTTG[C/T]GATTTTTCTGTTTTC	84708
rs755677755	snp	A/G			intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53559553	AAAAGAAAGACAATA[A/G]TAATAGTGCTTAACT	84708
rs755716156	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53587724	TAAGTGAGGAATTCA[A/T]ATATAGAAAGGAAGT	84708
rs755721441	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508592	TGTTTATTTTGACCA[C/T]GAAAGCCCTTAGTCA	84708
rs755742756	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53530773	GCAGCCAGTTAAAAC[C/T]ATAATTTTTGTTTAA	84708
rs755759741	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53541551	TTATATCAAATGGAA[A/G]AAGCAGGGATCTATT	84708
rs755768648	snp	G/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53500248	TGAGCCAGCAGCACC[G/T]ACTGGCATTGTTTTT	84708
rs755771278	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53588663	GAGGGGGCCTGTGAA[A/G]TACACCATTTTAGCG	84708
rs755794039	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53552470	GTGTGTGGAGAACGA[A/G]ATGCACCACCAGTAC	84708
rs755797237	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53641143	TGGCATGGTTTTTTG[G/T]CCTGGGTATGCTGGA	84708
rs755824691	snp	A/G	1.65548e-05	0.002877	synonymous-codon, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461015	TGATGTACTTCTACC[A/G]TTGACAGCAAGAAGA	84708
rs755838964	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53629866	GTTTGATTTTTAAAA[C/T]GAGTGATGCTGCTTT	84708
rs755854451	in-del	-/AA			intron-variant	LNX1	GRCh38.p7	4:53608782	ATACTATGCAGCCAT[-/AA]AAAGAATGAGATCAT	84708
rs755858795	snp	A/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53501609	TTTTCAGATGAAGAA[A/T]TGCTGAAGCTTAGAG	84708
rs755870976	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53551426	CAGCTTCCTAGTAAG[A/G]TCTCAGGAGTTGGGT	84708
rs755885914	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53472326	GGAACATCACACACC[A/G]GGGACTGTTGTGGGG	84708
rs755890473	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53495050	CAACTTTTATAGGGA[C/T]CTTTGTGGTGATGGA	84708
rs755905799	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53564323	AGTTCCAACAGCCAC[C/T]TGCTAGCCCTTCCCC	84708
rs755912897	snp	C/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53523660	TTAGTAGGAGACTAG[C/G]AGACTAGGGATTTTT	84708
rs755917613	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53551083	AACCTAGGAGGCGGT[C/T]GGTGGTTGGAATCCT	84708
rs755928010	snp	A/G/T	3.30111e-05	0.00406259	stop-gained, synonymous-codon, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508206	ATCTTTGGTCAGGCC[A/G/T]TAGTGGGAGGCACCT	84708
rs755932020	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53525202	CTAAAAGCTCTGGCC[A/G]GGCTGGGAGCAGTGG	84708
rs755934216	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53494938	TTTATATAACATTCT[G/T]GAAATTCAAAATTAT	84708
rs755939303	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53485699	ATATGCTTGTCCTGG[C/T]TTTAACTCCTATCAG	84708
rs755981130	snp	C/T	8.24178e-05	0.00641889	missense	LNX1	GRCh38.p7	4:53496286	GTCCATTGTTCCTGC[C/T]GCGGAACTTCTGTTC	84708
rs755998520	snp	A/G	1.64746e-05	0.00287002	synonymous-codon	LNX1	GRCh38.p7	4:53476821	CATGTTGTGGTTGGA[A/G]TCCAGGGCTGCTGGG	84708
rs755999246	in-del	-/AG			intron-variant	LNX1	GRCh38.p7	4:53464945	TTTTTTCTGAAAATC[-/AG]AACATTCTATAAAAT	84708
rs756001173	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53511836	ACCCAACAGGGCAGC[A/G]TGATCTGGGTTCCCA	84708
rs756008961	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53534641	AGCAACACCCTGTCT[C/G]TAAAAAAACATAATA	84708
rs756011482	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53623134	TTGAATACATTGCAC[A/G]GCTGGACTATATGTG	84708
rs756035359	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53648703	GCCTCACAGCTCCAA[C/T]AATGGGGGCTGAAAG	84708
rs756079062	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53582651	ACAAGGGCTAACTCT[A/G]TATCAGATTATTTCT	84708
rs756086455	snp	A/C	3.29511e-05	0.00405887	synonymous-codon, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507381	GTTGGCAACTGCACT[A/C]CCGCTCTTTGTCCTT	84708
rs756087518	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53649813	TTGAAATTTATTGCT[C/T]GTCTGCTTCCCACAG	84708
rs756117841	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53639508	ATATCCCAGAAAAAA[A/T]AAGGCATCTTGAAAC	84708
rs756120759	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53527552	GTTCTGGAGGGCAGG[C/T]TCCAGCCTCCTTTCA	84708
rs756124507	snp	C/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53603136	GGATCCAGAGCACCA[C/T]AGTGTCACTGTATTA	84708
rs756157034	snp	C/T	1.76674e-05	0.0029721	missense, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573990	GATCGTTGGCAGACT[C/T]TGGCTGGTTCATGAT	84708
rs756173605	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53631339	GGCAGAAGAAGGGAA[C/T]TTCCCTGTGGGCCTT	84708
rs756176942	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53563174	TCGTGCCAGCCTGGG[C/T]GACAGAGTGAGATTC	84708
rs756191896	in-del	-/T	1.64925e-05	0.00287158	intron-variant	LNX1	GRCh38.p7	4:53476748	ATGTTGTGTTTGGAC[-/T]TTACCGTGGTAATTC	84708
rs756193707	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53479758	AAAACACAATGGGTA[C/G]CTGAATATTTCTCAA	84708
rs756218786	snp	A/C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53515960	TGAGGTTTAAAGATT[A/C/T]GCACAAAAGGCCGAG	84708
rs756229675	in-del	-/GTGTGAGAGAGA			intron-variant	LNX1	GRCh38.p7	4:53652017	CAATTTGATGTGTGT[-/GTGTGAGAGAGA]GAGAGAGAGAGAGAG	84708
rs756247315	in-del	-/AAAAC	1.67778e-05	0.00289631	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461052	CCACATCTAAAAAAA[-/AAAAC]AAAACAAGATATGAT	84708
rs756253781	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53622328	ACTTTTCAAAGTGCG[C/T]GGATTAGAAATACTG	84708
rs756272134	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53626400	TAAATTTTAGGTATG[C/T]GAATTATAACTCAAT	84708
rs756281682	snp	A/C/G	0.000115829	0.00760935	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507464	TGGATCTCTCAAAGG[A/C/G]CCGTGCTGAGGAATA	84708
rs756291975	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53497894	TCCCTCAGCAACCTA[A/G]AAGGGATGGGATAGA	84708
rs756299998	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53613644	GACATGATCTAATTC[C/T]TTTTCATGGCTGCAT	84708
rs756313535	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53475101	AGTAGAGAAGTGCCA[A/T]GCCCAAGGGCAAATG	84708
rs756315919	in-del	-/TCTA			intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53559859	AGAGATGAGGGTCCC[-/TCTA]TGTTGCCCAGGCTGG	84708
rs756319276	in-del	-/C			intron-variant	LNX1	GRCh38.p7	4:53642562	TGTGGCACGGTTATT[-/C]TTTATATGCTTGGGG	84708
rs756322387	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53585138	GGATTCAGTGGAGTG[A/G]TCACTTCCTTAACCA	84708
rs756338227	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53487230	CTACTGCCTTGGCAT[G/T]GCATGAGTCCATACA	84708
rs756358873	snp	A/G	5.07447e-05	0.00503684	missense	LNX1	GRCh38.p7	4:53496034	TCACCTGAATCAGAT[A/G]AGCCGCACTTTCTGG	84708
rs756360991	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53538060	GTGATGAAATTTACA[C/T]AGCAATTGGTTTCAA	84708
rs756382880	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53573169	GTATGATGTCGTTGA[C/T]ATGAAGCACTTAGAG	84708
rs756387512	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53587615	CCAGCATCTTACAGA[C/T]GGCATTTCGAGTAGT	84708
rs756402583	in-del	-/TAAGTG			intron-variant	LNX1	GRCh38.p7	4:53492615	TAGGAGAGAGATGAT[-/TAAGTG]TAAGTGTGGAAGGCA	84708
rs756430984	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53610780	AGAAGAAGAATAAAG[A/G]GAGATAAATAAAGGC	84708
rs756435993	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508663	AACGTAAATATAAAG[C/T]TCCTCCCAGATTCCA	84708
rs756482012	snp	C/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53596410	TTGGCGCACATTTTG[C/T]GAAAGTTTACCACAC	84708
rs756503462	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53625474	GAAAAGATGTTCAAC[A/G]TCATTAATAATTTGG	84708
rs756520285	snp	C/G	4.94197e-05	0.00497066	missense	LNX1	GRCh38.p7	4:53496107	GTCATTCTCCTCAAG[C/G]TGACCATGTCGATAT	84708
rs756526927	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53463863	TATTACTAATTTAGT[C/T]AATACATATTTGAGA	84708
rs756556920	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53537243	GAGTCAAACACCAAA[C/G]AAATTATAAAGGAAG	84708
rs756568473	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53573094	TACACCCTCTCTGGT[A/C]TATTTCACATTTCAA	84708
rs756578801	snp	A/G	2.80352e-05	0.0037439	missense, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573645	GAAAGTGATGCTCGA[A/G]GTCACAGCGCTGCAA	84708
rs756580885	snp	C/T	0.000117872	0.00767607	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498609	TTTTTATATCAAGCC[C/T]CTTGCTGCAGCCCCA	84708
rs756581145	snp	A/C			upstream-variant-2KB	LNX1	GRCh38.p7	4:53652768	TATAATCCTTGGCAT[A/C]TTTTATTTTTGAATA	84708
rs756601843	in-del	-/ATC			intron-variant	LNX1	GRCh38.p7	4:53490184	ATGAAAGCCCCTATT[-/ATC]ATTGGCTCTAGAAAT	84708
rs756608102	snp	A/G	1.65375e-05	0.0028755	intron-variant	LNX1	GRCh38.p7	4:53476710	TTAAGAAATGTAATC[A/G]TTTTCTCCCACGCCC	84708
rs756613503	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53635918	TAAATATTTACTAAG[C/T]GTGCATAAAATAGCA	84708
rs756632786	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53607215	CACCTAGAAAATTCC[A/G]TAGTCTTTGCCTAAA	84708
rs756633120	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53479930	GTGCACTTAGTCGCT[C/T]TATGACTCTTTCTGC	84708
rs756649310	snp	G/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53595747	AGGTCTGTCTTCAAA[G/T]CTCTTTTCTTGTAGA	84708
rs756661997	snp	A/C	1.69666e-05	0.00291256	intron-variant, utr-variant-5-prime	LNX1	GRCh38.p7	4:53558000	CTTCTCCCTGGCCAC[A/C]TTCTGTCAGCTACAA	84708
rs756691236	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53560974	ACTCTAATCTTTGCC[A/C]TATTCTTTGCCTGGC	84708
rs756696703	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53520189	TGCTGAAGGCACAGC[C/T]TCTCACAGCAACCCC	84708
rs756715156	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53505984	GCATGCAGCATGTAC[A/G]TGCAGGGTGAGAGGC	84708
rs756730579	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53547780	ACAGGAAAATATGAG[A/G]GAATAAGAAGAAGGA	84708
rs756764845	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53608184	AGTAAACAGACAGCC[A/T]ACAGTATGGGAGAAA	84708
rs756782813	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53561779	AATTATTGAACAATG[A/G]ACTCTGTATTCATAC	84708
rs756784897	in-del	-/AAT			intron-variant	LNX1	GRCh38.p7	4:53472099	ACCCAAATTTCCAAC[-/AAT]GATAGACTGGATTAA	84708
rs756803804	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53637263	TTTACTTTCTTCACA[A/G]CTGTAGTTCTCAAAC	84708
rs756804674	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53502630	AACAATGAAGTTTGC[C/T]ACATGAACTGACTCT	84708
rs756816021	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53548850	TATGCAGCCATAAAA[A/G]AGAACAAGATCATGT	84708
rs756818987	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53589401	AATTAATTACAATAA[C/T]AAGAACTATCAAGGT	84708
rs756833792	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53494881	ATCAGAACATTATAC[C/T]GGGTGAAAAAAGCCA	84708
rs756838864	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53647358	ATAATATTAATCTTA[A/T]TTGTTTTAGGAAGCA	84708
rs756869870	in-del	-/TTCAC			intron-variant	LNX1	GRCh38.p7	4:53528394	GTCATAGCTATGTCA[-/TTCAC]TTCACTTCATCTCAT	84708
rs756880177	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53482027	TTGCCAAGAGCATGA[C/G]AGCTCTTTCCTTTAT	84708
rs756880518	in-del	-/A			intron-variant	LNX1	GRCh38.p7	4:53638325	TTAGCAAGACTGTAC[-/A]ATATAGGTATAGTCA	84708
rs756884427	in-del	-/G			intron-variant	LNX1	GRCh38.p7	4:53555907	TTTTAAGTGGTATAA[-/G]GACCTTCCTTCAATT	84708
rs756886596	snp	A/G	3.62234e-05	0.00425563	utr-variant-5-prime, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53574012	GTTCATGATGGATTG[A/G]AGAGCAGTATAACAG	84708
rs756889564	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53550837	GTCTTGCCACACAGC[C/T]TTCACCTAGAGAAGG	84708
rs756919256	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53607298	GTACAAAAATCACTA[C/G]CATTTTGTATACACC	84708
rs756985376	in-del	-/AATCATGCTGC			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53605863	AGCTTGGCTATTATG[-/AATCATGCTGC]AATCAACAACATGGG	84708
rs757041921	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53514060	ATTCCCATCCAGTTT[A/G]TTCCTGCATCTCCTT	84708
rs757054456	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53588747	CTCCCTTAGGGCTCC[A/G]TAGGCAAGCTAGTAG	84708
rs757058076	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53514551	ACTTATTCACTACCA[C/T]GAGAACAGTATGGGG	84708
rs757064953	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53630065	ATGAGTATTTTCCCA[A/T]GAAAATAGTTTCTTC	84708
rs757078893	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53485799	GTGTGAGTGTGAGGA[A/G]GGGGAGTATAGGGGA	84708
rs757087928	snp	A/G	9.97324e-05	0.0070609	intron-variant	LNX1	GRCh38.p7	4:53478755	GGGCTGAAGGCACAG[A/G]TGGAAAAACATGGCA	84708
rs757095991	in-del	-/CT			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53594154	AATATATATATATAT[-/CT]ATGTATATATAAATA	84708
rs757101737	in-del	-/C	1.66399e-05	0.00288438	frameshift-variant	LNX1	GRCh38.p7	4:53481778	CCATTGCTGTTCCAG[-/C]CGGCTTCCTGAAAGA	84708
rs757101821	snp	C/T	1.68439e-05	0.00290201	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508013	TGCTCCGGCCAGAGT[C/T]CACTGGGCTGATTGC	84708
rs757136739	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53542659	AGAGAAAATCCATGA[C/T]AAAGACATGAACAGA	84708
rs757140151	in-del	-/A			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53598199	TGTTCTGCACTCGTG[-/A]CATACTCTACTTCAG	84708
rs757144764	snp	A/G	1.6473e-05	0.00286988	missense	LNX1	GRCh38.p7	4:53496163	AGATGAAAACCCCAG[A/G]CTCATCCACCTTGCG	84708
rs757156927	snp	C/T	1.65935e-05	0.00288036	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508082	TGTCTAGGCCAGGCT[C/T]GTCTGTCATTAAGGA	84708
rs757168865	snp	C/T			nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53604177	ACTGCTGATTTTTGT[C/T]CTACCCTTCGTAGAA	84708
rs757198156	snp	A/G	1.675e-05	0.00289391	missense	LNX1	GRCh38.p7	4:53496354	CGCAGGAGACGCACA[A/G]CGTAGTTGTGAGGGA	84708
rs757226242	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53641423	CTTCACTCTAGTAAC[A/G]TTATCCAGGCAGTGC	84708
rs757262631	snp	A/G			upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53592555	AACTGTGGATTCCCC[A/G]TCCCGGAAGATGGCC	84708
rs757268575	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53571864	TGGGGTCTTGCTATG[C/T]TGTCCAGGCTGGTCT	84708
rs757281235	snp	C/T			intron-variant, utr-variant-5-prime	LNX1	GRCh38.p7	4:53558029	AAGGGCCCAAACCAG[C/T]CAAGCTCCTTTAAGC	84708
rs757299870	snp	A/G	1.64768e-05	0.00287021	synonymous-codon	LNX1	GRCh38.p7	4:53476913	ATGATGTTCTTTTCA[A/G]TAATGCCACTGCCTC	84708
rs757303003	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53587539	GCTACTGGGAAGTCC[A/T]TGAATACTGAGGCAA	84708
rs757322072	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53545131	TCAATTAGCTCATGC[A/G]GCCAAAAATATTTCT	84708
rs757325453	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53504504	AACTTTCTCCATATC[A/G]GCAATAAGGCTGTTT	84708
rs757338555	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53533477	GTTCTCAGCTCACCG[C/T]AACTTTTGCCTCCCA	84708
rs757339182	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53505901	GGAGCGCAGGCTGGA[C/T]AATGGAAGGGAGGTG	84708
rs757341002	snp	C/T	1.9765e-05	0.00314358	missense, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573771	CCAGAGGCTTGCGGT[C/T]CATGGGACAGAAGTC	84708
rs757346292	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53546466	TAACCACTAGCTCCA[A/T]TTTTATTGCTTCCTC	84708
rs757379714	snp	A/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53516512	TTGGGGTAATTGGAG[A/T]AGGCTTCTTAGAAGA	84708
rs757401803	in-del	-/C	6.78357e-05	0.00582351	intron-variant, utr-variant-5-prime	LNX1	GRCh38.p7	4:53557999	CCTTCTCCCTGGCCA[-/C]CTTCTGTCAGCTACA	84708
rs757449816	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53586136	TGCAAAGGGCCTCAA[A/G]GGAAAAAAAAAAGGC	84708
rs757469473	snp	A/G	3.43342e-05	0.00414318	synonymous-codon, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573886	GCAGATGTGGCAGAT[A/G]AGGTCATCATCCACT	84708
rs757471467	snp	A/G	0.000100981	0.00710496	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498883	TTAAGACACCCACCC[A/G]ATGGACCTTTCCAAC	84708
rs757475626	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53471512	TAATTAAATGAAAGA[C/G]CTTCTGCACAGCGAA	84708
rs757488805	in-del	-/CTC			intron-variant	LNX1	GRCh38.p7	4:53463619	TATTCTGCACTCATT[-/CTC]CTCTAAATTTAGGCC	84708
rs757502547	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53515979	CAAAAGGCCGAGTGT[A/G]GTGGCTCATGCTTAT	84708
rs757506657	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53528831	TGTGATCAAACCTAG[A/C]CAATCAGGACATCCA	84708
rs757508589	in-del	-/AGG			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53594027	TACCCATTATTCAGA[-/AGG]AGGAGAAGTAGAAAC	84708
rs757509713	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53476375	ACTAGCAGATTAGGC[A/G]AAGGTGAACCTTCTC	84708
rs757521282	snp	C/T	1.64751e-05	0.00287007	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507358	TTTTCCCTGCCCTGG[C/T]CGGCATGGTTGGCAA	84708
rs757539859	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53510638	GAAAAAATAAAAGCC[A/G]ACTTGCATTTGAGCG	84708
rs757546856	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53557158	TGAGGCATTTCCTTG[C/T]ATAAAATGGACATGT	84708
rs757551751	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53643334	TTTAAGTTTTTTGTA[A/G]AGACAGGGTCTCCCT	84708
rs757565527	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53572699	GAACATGACAATGTA[A/G]GTGGACAAAATGAGA	84708
rs757584571	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53610359	CCATCTTAAAAGCCA[C/T]GAAAGGTCGAACTTT	84708
rs757603194	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53632483	AGAGGGTCAGTCAGA[C/T]AATGATCGACTGACT	84708
rs757609521	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53488469	AGTTCTGGACTCGCT[C/G]TAATAAAGTTGTGTG	84708
rs757620607	in-del	-/AAT			intron-variant, cds-indel	LNX1, FIP1L1	GRCh38.p7	4:53462005	GGCAAAAATCCTTTG[-/AAT]AATCTCAATGAAAGC	84708
rs757646616	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53484113	CCAGACACCAAACCG[A/G]CTAGTGTCTTGATCT	84708
rs757665685	snp	C/T			intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498952	CTATTCATTTTTCCT[C/T]ATACATGTTTTCCAT	84708
rs757702916	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53509661	AAATTCATTAAAGTC[A/G]TCATGGTATCTACAT	84708
rs757707563	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53465492	AGGCACTGTATTAAG[C/T]TACATTCTTCTCCAG	84708
rs757724392	in-del	-/T			intron-variant	LNX1	GRCh38.p7	4:53494171	GAATCACGGGAGTGG[-/T]TTCCCCCATACCATT	84708
rs757737946	in-del	-/C			intron-variant	LNX1	GRCh38.p7	4:53532891	TGCTGCCAGCATCAT[-/C]CTGTTCCAAATATTT	84708
rs757744785	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53549705	GAGATATCGATAAGA[C/T]GGCCTTGAATTCACA	84708
rs757757611	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53625615	CAAACTGGGCAACAT[A/C]GTGACACCCTGTCTC	84708
rs757758546	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53628620	CGCAGCAGTCCCACT[C/G]TTGGGTACCTACCCA	84708
rs757765550	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53464474	ATAAAATGTTTTAAT[A/G]TAATCAACATGAAAA	84708
rs757776029	in-del	-/AA			intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461628	TGTACATGCATATTT[-/AA]AAGTTTCACAGTTAA	84708
rs757798870	snp	A/C			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53597212	TCTCCTTGGCAAACT[A/C]TCAATTGATATTCCT	84708
rs757808954	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53626593	CAGCTTAGCAGGGCA[C/T]CAGAAGCCTTATGAA	84708
rs757816453	snp	G/T	1.64784e-05	0.00287035	intron-variant, stop-gained	LNX1	GRCh38.p7	4:53557915	GCCCACATTGTCAAT[G/T]TAGTTAGCAGGACTG	84708
rs757825002	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53537304	GTAAACAACACCCTT[G/T]AAGTCCTATGTGTGC	84708
rs757842638	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53525832	AGGGCTGTGTTGGGG[C/T]TGGTGTGGGGAGGCA	84708
rs757846207	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53585365	AGTATTTCAGCCTCC[A/T]AGTGGACAAGAAATC	84708
rs757869416	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53492236	ACAGTTGAGAGGAGA[A/C]CTGAATGAACTGTGG	84708
rs757870438	snp	A/G	0.000133618	0.0081726	missense, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461456	CTTCCATCATTGTAT[A/G]CTGGTGTTCCTTCAA	84708
rs757921177	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53551350	CTCTCTAAAATAATC[A/G]TTGGTTGAAGCCAGG	84708
rs757924195	in-del	-/ACAA			intron-variant	LNX1	GRCh38.p7	4:53466928	GGGGGCAGGGCACAG[-/ACAA]ACAAAAGGCAGCAGT	84708
rs757925168	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53562953	CAATGGCTCAAGCCC[A/G]TAATCCCAGAACTTT	84708
rs757926698	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53608331	CACTTTTTAAAAGAA[A/G]ACATACAAGCAGTCA	84708
rs757966042	in-del	-/C			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53599389	ATGCCACGGCAACAT[-/C]AGGAAGTTACCCTAT	84708
rs757967861	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53484168	TGAGAAATAAATTTA[C/T]GTTGTTTACAAGCCA	84708
rs757984712	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53621608	CACTCATATAACTCC[A/G]GTCAGTTGTCTGGTT	84708
rs757994257	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53510887	CAGCATGTCCTAGTA[A/G]AAGAAACTGGCACCT	84708
rs758095654	snp	C/T	1.8336e-05	0.00302782	missense	LNX1	GRCh38.p7	4:53496394	TGTCCATCCCGTTGA[C/T]CTGGGGGCAGGTGGA	84708
rs758109806	snp	A/T			intron-variant, utr-variant-3-prime	LNX1, LOC101928879	GRCh38.p7	4:53576939	TTCTGTACTGCAGTA[A/T]TATGCCTGAGAGGAC	84708
rs758110065	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53647564	CACTGGTCCACTTTG[C/T]TAAGAAAAAAAAGCC	84708
rs758133667	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53609214	TGTATACAAAACCCC[C/T]GTGACATGCAATTTA	84708
rs758141715	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53624076	GGGCCCTCCATGACT[C/G]CTTTTCTTGAGCTCT	84708
rs758160484	in-del	-/CT	1.75928e-05	0.00296582	frameshift-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573988	AGGATCGTTGGCAGA[-/CT]CTGGCTGGTTCATGA	84708
rs758160664	snp	C/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53515813	AAAGAATCTGGATGT[C/G]AATCCCAGATCTGCC	84708
rs758160861	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53638204	TTATTTCTCTGACTT[A/G]GCTTCTCTGCTGGGT	84708
rs758162977	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53648371	CCATTAGTGATGAGG[A/G]TCTTTTCCTGTGCTT	84708
rs758163190	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53580040	TTGGCACTTTAACCT[C/T]GTCAAAGATGAAACA	84708
rs758165542	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53580543	TTACTGGAGTGGGTA[C/G]AGGAGGAGACACTGC	84708
rs758196849	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53579615	AGGGTCATTCGAGAT[C/G]GTGTGTCTACTGTCA	84708
rs758215883	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53620307	ATTTTGCATTATAAC[C/T]TGTGAACATATTATA	84708
rs758221988	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53561229	TAGTCCCCTGTATTT[A/C]TTTTCTTTTCTTTTT	84708
rs758222945	snp	A/G			intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53559609	GAGGCAATGCCCATA[A/G]ACAACAAAGGGCTTA	84708
rs758242044	snp	C/T	1.79548e-05	0.00299617	utr-variant-5-prime, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53574005	CTGGCTGGTTCATGA[C/T]GGATTGGAGAGCAGT	84708
rs758242769	snp	A/C	1.64863e-05	0.00287104	missense	LNX1	GRCh38.p7	4:53478597	TCTCTGCTTATGACT[A/C]CTCCGGGCTCAACAC	84708
rs758250694	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53504249	TGCTTCGTTACAATC[A/G]GCATCTGCTGCTTCG	84708
rs758253773	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53473983	AGACCAAGCCACATA[C/T]GGAGGGAAAGAAATG	84708
rs758262099	in-del	-/TTTTTT			intron-variant	LNX1	GRCh38.p7	4:53545803	ACTTCAGAGGCCACA[-/TTTTTT]TTTTTTTTTTTTTTT	84708
rs758281430	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53532169	TCACAATATATTGAG[G/T]GTTCCCTTCAAGAAA	84708
rs758285138	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53514613	CGGGTCCCTCCCACA[A/G]CATGTGGGAATTAGG	84708
rs758288066	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53621562	GCCTCTGCAGTGAAT[C/T]GTACCTAAGGATTTA	84708
rs758297456	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53644071	GGTAGACTGCACTTA[C/G]TATGTTTTGTACTTC	84708
rs758302674	snp	A/G	1.65625e-05	0.00287766	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507469	CTCTCAAAGGGCCGT[A/G]CTGAGGAATAGCGAC	84708
rs758332865	snp	A/G	6.59022e-05	0.00573993	synonymous-codon	LNX1	GRCh38.p7	4:53478665	TGCTCCCCCTGCGAC[A/G]GTCATGCCGAGAGAT	84708
rs758349941	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53642493	TGATGGGTCCTGAGG[G/T]GCCAGCACCAGCTAG	84708
rs758359121	snp	A/C			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53601755	TCTATGAGGCTCCAG[A/C]TCTACTTTCAACTCA	84708
rs758360218	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53589777	TTGTGTGTAAATTAC[A/C]CAACAGACCAACTGC	84708
rs758360319	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53474917	GACTACAGGCGTGTG[C/T]CACCACGCTTGGCTA	84708
rs758361654	snp	C/G			intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53462520	TATTTTGTTTATATA[C/G]CGTACCTTAAAATAT	84708
rs758364177	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53556615	AAAGCTTCTGCAAGG[A/T]CATTATTTCCTCAGA	84708
rs758386673	snp	C/G	1.65053e-05	0.0028727	intron-variant	LNX1	GRCh38.p7	4:53476729	TCTCCCACGCCCCTA[C/G]AGGGATGTTGTGTTT	84708
rs758395029	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53582765	TTTGGATTAAGCTCC[A/G]TGTGGCAGAATGGTT	84708
rs758406769	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53488182	AGTACCCCCAATGAC[A/C]GGGAGCTCACTGTGT	84708
rs758424595	snp	A/T	9.88403e-05	0.00702925	missense	LNX1	GRCh38.p7	4:53496233	GTTGAGAATCACATG[A/T]AAGCTGTCATCTCGG	84708
rs758440004	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53564532	TGGGGTGGGCAGAAT[A/C]ATTATTCCCCAGAGA	84708
rs758451765	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53542802	TTTAAATCTGTATTC[A/G]GAACACGTGACCCAG	84708
rs758461362	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53534746	ACAAGAAATATCTCA[A/T]CTGTCTTCTGTACTC	84708
rs758468436	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53495706	TGCCACCACACCTGG[A/C]TAATTTTTTGTATTT	84708
rs758475830	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53524038	CATAAAACTTACATT[A/T]TAGATAAGGGTCTTT	84708
rs758485876	snp	A/G	1.67298e-05	0.00289217	synonymous-codon, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461449	CCTAATTCTTCCATC[A/G]TTGTATGCTGGTGTT	84708
rs758539547	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519064	CTGCATGCCTCATAG[A/G]TCAGTGCATGGGGGA	84708
rs758542966	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53583834	CACCTTTCCCCTGGG[A/G]TGCCATACTTGGGTT	84708
rs758544058	in-del	-/AATT			intron-variant	LNX1	GRCh38.p7	4:53590705	TTGCAGCAATGAGGG[-/AATT]AATTCTTACTGTAAC	84708
rs758554596	in-del	-/TGTGAG			intron-variant	LNX1	GRCh38.p7	4:53652018	AATTTGATGTGTGTG[-/TGTGAG]AGAGAGAGAGAGAGA	84708
rs758570307	snp	A/G	1.64746e-05	0.00287002	synonymous-codon	LNX1	GRCh38.p7	4:53476812	GGGTGGGGCCATGTT[A/G]TGGTTGGAGTCCAGG	84708
rs758572179	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53606447	CAGTAACAAAAAGCC[C/T]ACCAACCAGAAAAAA	84708
rs758572768	snp	A/C			upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53592793	GGAAGAAAAGGAAGT[A/C]CGGATTCCCACAGCC	84708
rs758598553	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53518240	ACCTAAGCAAGCACA[C/T]TGACTTGGTTTACCA	84708
rs758603680	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53478120	CTGGGAAAGTATCCA[C/G]CATGATACTTTCACT	84708
rs758603929	snp	C/T	2.50404e-05	0.0035383	missense, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573671	TGCAACACCTGGGTG[C/T]AGTGCTCCCTGAATG	84708
rs758616052	in-del	-/TCC			intron-variant	LNX1	GRCh38.p7	4:53523857	CACACTGTCCCACCA[-/TCC]TCCTGCTTCCCCTGG	84708
rs758623644	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53557302	CAAATGTGGCAAAAT[A/G]TTAACCCATTAAATC	84708
rs758633692	snp	A/G	1.65102e-05	0.00287312	missense, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498838	GGTGGTACAACCTTG[A/G]AAAGACTGAAATGGA	84708
rs758634548	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53506025	AAGTATACAAGAAAA[A/G]GTCTGATAAGGCTGC	84708
rs758646118	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53643668	CTTCTCCCTCCTGTT[A/G]AGAGCTTTGGAGTGT	84708
rs758662572	in-del	-/GAT			intron-variant, downstream-variant-500B	LNX1, FIP1L1	GRCh38.p7	4:53463039	GAAAGGTAAGAATTA[-/GAT]GATTGTTATCTAAGG	84708
rs758667336	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53626585	GTAGAGAACAGCTTA[A/G]CAGGGCATCAGAAGC	84708
rs758685135	in-del	-/A			utr-variant-3-prime, downstream-variant-500B	LNX1, FIP1L1	GRCh38.p7	4:53460293	ACAAAACAAGTTTAT[-/A]AATTAATTCTCTGAG	84708
rs758718629	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53628185	AAGACTCTTCTTGAA[A/T]ATAATCATCAGGAGA	84708
rs758724920	snp	C/T	2.07024e-05	0.00321726	missense, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573740	AGGATGCTGGACTTC[C/T]TGCAGTGCTGCAGAA	84708
rs758734454	snp	A/G			nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53604432	TAGACTTAAAAGCCA[A/G]TTGGATAAAAAGCAG	84708
rs758760499	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53627597	TCAAATGAAAGAAAA[G/T]AAAATTCAAATTAGA	84708
rs758768130	in-del	-/T	1.70644e-05	0.00292094	splice-acceptor-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461043	GAATATCACCACATC[-/T]TAAAAAAAAAAACAA	84708
rs758793252	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53539788	ATCAAAGATATTGCT[C/T]GCTTCATATTTTCAA	84708
rs758795239	in-del	-/TATTT			intron-variant	LNX1	GRCh38.p7	4:53535546	TAGATTTTATCATTC[-/TATTT]TATTTTGTTAGTGAA	84708
rs758803066	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53644477	AAGTGACTTAAGCTA[A/G]ACTGATGTATTATAT	84708
rs758814258	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53489984	AGTACCACAAAAGTT[C/T]TACCCTTTTTTGCAG	84708
rs758823053	snp	A/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53505461	TTCACTGTGTTGGCC[A/T]GGCTGGTCTCAAACT	84708
rs758864236	snp	C/G/T	3.29501e-05	0.00405884	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507355	GAATTTTCCCTGCCC[C/G/T]GGTCGGCATGGTTGG	84708
rs758871759	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53484431	AGCCAGTCGTGGTGG[C/G]AGGCACCTATAATCC	84708
rs758886486	snp	C/G			intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53499175	TACCTTTTTGTTTTT[C/G]TTTCTGTTTTTTGAG	84708
rs758934589	snp	A/G			upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53593430	ACCGAACAGCCTGGA[A/G]ATCGTGAGGTTTCAC	84708
rs758936938	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53489352	ATGTTCCCAGAAGCA[G/T]GTATCTTTAGATGCA	84708
rs758962360	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53571474	GAGCCTGGAAGATGC[C/T]ATGCGGCTGGCTCTG	84708
rs758980725	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53553495	GAACCTACACTGTTC[G/T]AAGGTTTTCATCTAC	84708
rs758987146	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53587455	CATTGTCAGAGGACA[A/G]TAAATTTGCCAACCA	84708
rs759026722	snp	A/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53599790	CTATGTATGTCACCC[A/G]AGAAAACCTATACCT	84708
rs759027024	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53625418	AAGGATTTGAATAGA[A/T]ATTAATCCAAAGAAA	84708
rs759034133	snp	A/G			intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53575168	TGTATTTTTAGTAGA[A/G]ACAGGGTTTCGCCAT	84708
rs759060753	snp	C/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53602667	AGATGGGGAGTGGAG[C/T]CCACAGGACCCAAGT	84708
rs759081807	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53537115	GTAGTGGGGACGGTA[G/T]GAGTACTGATTTTCC	84708
rs759086035	in-del	-/TT	4.95176e-05	0.00497558	frameshift-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460938	GCCAAGAAACAATAG[-/TT]TTAGAGTAATTCTTC	84708
rs759092496	snp	C/T	1.64849e-05	0.00287092	synonymous-codon, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507414	AAGAACACTCAAAGC[C/T]CGATTTATTTTTTTA	84708
rs759098910	snp	G/T			missense	LNX1	GRCh38.p7	4:53481800	CCTGAAAGATGTCAG[G/T]GCTCCGCTGCCGAAC	84708
rs759110642	snp	C/T	5.07189e-05	0.00503556	missense	LNX1	GRCh38.p7	4:53481820	CGCTGCCGAACCTGG[C/T]GGGACACGACGAGGT	84708
rs759128981	snp	A/G	1.79609e-05	0.00299669	intron-variant	LNX1	GRCh38.p7	4:53481885	CAGGCATTAGCCACT[A/G]TCAGTTTCCATCCAC	84708
rs759131054	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53535709	GGCTCTATAGCCAGC[A/G]CCTTACATATGCCAT	84708
rs759133088	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53561194	AGCAAGACTAATACA[C/T]GCTTACTTTTCATAG	84708
rs759164548	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53650307	GTAGCTCCAGAATTC[C/T]AGGAGCCAGCTCAGG	84708
rs759168902	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53478424	TCTATACTCAAACCA[A/G]TCATGGTCAATGGGT	84708
rs759176935	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53624771	TCTACCTCCTGGAGC[A/C]CTGCACGTGCACAGT	84708
rs759191802	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53612241	TAACACTTATTGCTG[G/T]CAGGTTAGTAGGTAA	84708
rs759196273	snp	A/G			missense	LNX1	GRCh38.p7	4:53496180	TCATCCACCTTGCGC[A/G]CCAGTTTTATTCCAA	84708
rs759216838	snp	A/G	1.66114e-05	0.00288192	missense, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461528	TCATAACCTCCTACA[A/G]TGCAGAAGCCCAGAC	84708
rs759222269	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53622779	GCTGGAAAGATGAGA[A/C]TAAGAGAGGGAGGCT	84708
rs759245743	snp	A/G			intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53462324	ATTCAGTGGCCCCCA[A/G]TGGATCAGTGTTCAT	84708
rs759260486	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53647457	ACAATGTCTCAGCCA[A/G]TGATGGAGAATATGA	84708
rs759280896	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53564183	TTCATCAAGCCTCTA[C/T]CTCAGGCTTCCTTGA	84708
rs759286567	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53583473	CTAAATCAATGATCT[C/T]GAAGAGGGACTAAGC	84708
rs759295848	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53506689	GAGAAACCCCGTCTC[C/T]ACTAAAAAATACAAA	84708
rs759324188	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53589130	AAAAAGAACTCTCTG[C/T]CAAGTCAGATTACAG	84708
rs759349994	snp	A/C	1.64781e-05	0.00287033	intron-variant, missense	LNX1	GRCh38.p7	4:53557890	GTTCTGAATACAGGA[A/C]GTGCAGGTTGCCCAC	84708
rs759368710	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53478866	AGCTGCATAAATTAT[G/T]CAAAGTGCATAAATA	84708
rs759374028	snp	G/T	6.91419e-05	0.0058793	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461620	TGTAATCAGTGTACA[G/T]GCATATTTAAGTTTC	84708
rs759377401	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53547128	TCGAAGACTATGTCT[A/G]TTGTGAGGCGCACCA	84708
rs759377481	in-del	-/TAGA			intron-variant	LNX1	GRCh38.p7	4:53609859	ATAAATCATGTAATT[-/TAGA]TAGCATTATATATAA	84708
rs759392243	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53490705	GGCAAATGTGATTCA[C/T]GGAGTAGACATACAA	84708
rs759395135	snp	A/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53593977	AGGTTCTGATTTCAT[A/G]CTCACTGGGACACTT	84708
rs759396289	snp	C/T			nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53605044	ATAGTGAAGTGGAAG[C/T]TGCCAGCTCAGTTAA	84708
rs759429855	in-del	-/T			intron-variant, splice-donor-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53523274	TTTAAAGCTGTACAA[-/T]TTTTTTTTGTTTGTT	84708
rs759444348	snp	A/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53594994	TGGGATTACAGGTGC[A/G]AGCCACTTGGTCCCC	84708
rs759455072	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53546691	TATGGTTCTGGGCCA[C/T]AGACACCACCAGCCA	84708
rs759456744	snp	A/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53516336	AATTATTGTCTAACA[A/T]CAAGGCATAATGTTA	84708
rs759474577	snp	A/G	1.65877e-05	0.00287986	intron-variant, utr-variant-5-prime	LNX1	GRCh38.p7	4:53557971	GCGCCTTCATTCTCC[A/G]AGCAGTGTGCTGCCT	84708
rs759483159	snp	A/G			upstream-variant-2KB	LNX1	GRCh38.p7	4:53654206	GTGCAGTTTTTAGAT[A/G]TGTTTATGGACTCTG	84708
rs759484056	snp	C/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53596582	CAGGGTGGATTATTC[C/T]CAGGGAATTTTTTGG	84708
rs759497959	snp	A/C/T	0.010326	0.0711159	intron-variant	LNX1	GRCh38.p7	4:53496427	AATCGTGCGGTCAGC[A/C/T]CCACCTGCCACAACC	84708
rs759509262	snp	C/T			intron-variant, missense	LNX1	GRCh38.p7	4:53557902	GGAAGTGCAGGTTGC[C/T]CACATTGTCAATGTA	84708
rs759528160	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53631861	AGGTGGAGCCTGAGC[C/G]TTTTTTTTTTTAAGT	84708
rs759539158	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53572205	ACTTCTTTCCCACCA[A/C]CGTCTCCCATACCTG	84708
rs759562786	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53477432	AAACTACCCATGAGA[G/T]TGTCTGGCAGAGGAG	84708
rs759574249	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53465325	TTAGCATGAATAGTT[C/T]GTTATGATTAGCTTC	84708
rs759582523	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53509859	CACTGCAAACCCAGT[C/T]GCACGAGTACCCCTT	84708
rs759585962	snp	A/G	4.95405e-05	0.00497673	synonymous-codon, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460958	AGTAATTCTTCCTTT[A/G]AGTTCTTTCAGCAGT	84708
rs759603327	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53585067	TAGTTTGTTAAGGTC[A/C]CTTTGAAAACCCGTA	84708
rs759607713	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53644979	TAGCCCCAGCCCTGA[C/G]ACCTAACTCCTCAAT	84708
rs759623194	snp	A/G/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53520823	AAAAATTAGTTGGGT[A/G/T]TGGTGGTGAGTGCCT	84708
rs759632502	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53626297	TTTGGGGTCATAAAA[A/G]TGTTCTGAAATTTAA	84708
rs759640428	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53564060	TGTGGGCGCCTGTGA[A/G]GGACTCACTCACAGG	84708
rs759657697	snp	C/T	9.88435e-05	0.00702937	synonymous-codon	LNX1	GRCh38.p7	4:53496227	ACTTTTGTTGAGAAT[C/T]ACATGAAAGCTGTCA	84708
rs759661554	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53537952	GACAGAATATCCTAA[A/G]GCTGGGGGAGAGAGC	84708
rs759663784	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53493059	ACTGAAACCTCCGCC[C/T]CCCGAGTTCAAGCAG	84708
rs759671063	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53549431	CTCCTTTGTATCGGC[A/G]GAGAATGAAGAACGG	84708
rs759680662	snp	A/G	1.66186e-05	0.00288254	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508072	TAGGCAGGGTTGTCT[A/G]GGCCAGGCTCGTCTG	84708
rs759688805	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53646978	TAAAAGGCAGGAAGT[A/G]TCCCGGCAGCCAGAG	84708
rs759708148	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53510415	GAGTTTGGTTATACA[A/G]CCTTATGTCCTCATC	84708
rs759711127	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53509322	CAAAACCCTATATGA[C/T]TGAGCTATTTTAAAT	84708
rs759732018	snp	A/C/G	3.29996e-05	0.00406189	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508163	TCGCACAGCCGTCTG[A/C/G]ACAGCCATCTTGTGA	84708
rs759733462	snp	C/T			intron-variant, missense	LNX1, LOC101928879	GRCh38.p7	4:53576233	CTCGCTTCCTGCAGC[C/T]GAGGGTCCTGATGCA	84708
rs759751748	in-del	-/GGCCCTT			intron-variant	LNX1	GRCh38.p7	4:53613985	CTGTTATTTTTTGAC[-/GGCCCTT]TTTTGATAATAGCCG	84708
rs759793728	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53615867	ATCATGGAGAATGGG[G/T]TATCCATCCCCTCAA	84708
rs759810177	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53608780	GAATACTATGCAGCC[A/G]TAAAAAGAATGAGAT	84708
rs759868957	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53530751	GGCATGCCAAAGACA[A/T]GACTATGCAGCCAGT	84708
rs759892916	snp	C/T	1.65638e-05	0.00287778	intron-variant	LNX1	GRCh38.p7	4:53477010	AAGCAGAAGCTATCT[C/T]TAGTGAGAGCACAAA	84708
rs759899218	in-del	-/ACA			intron-variant, utr-variant-3-prime, downstream-variant-500B	LNX1, FIP1L1	GRCh38.p7	4:53459935	TACATTTTTGATATC[-/ACA]ACAACTTTTTGATGG	84708
rs759906143	snp	C/T	1.64776e-05	0.00287028	missense	LNX1	GRCh38.p7	4:53496270	TAGGCATCCGGGGCC[C/T]GTCCATTGTTCCTGC	84708
rs759917690	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53646514	TTCCCAGCATCCAGA[A/G]CAGTGCCTGGCACAG	84708
rs759939213	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53470854	AGGATACAAACAAAT[G/T]GAAGAACATTCCATG	84708
rs759971289	in-del	-/C			upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53592084	AACACTTTTGCGCTA[-/C]CCCCTCCCCCGCCCA	84708
rs759993330	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53542370	GGATTGAGCTGAATG[A/C]GCAGTGTCTTGGGAT	84708
rs760001997	snp	C/T	1.64735e-05	0.00286993	missense	LNX1	GRCh38.p7	4:53476880	CTTTGACTTCCAAAG[C/T]TTTGAGTACTATCGA	84708
rs760111338	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53543662	CTGTTTCTGTAAACC[A/G]CTATTTTTATTAATA	84708
rs760119641	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53476112	GACCAGCCTGGGCAA[C/T]ATGGTGAATCCCCGT	84708
rs760126360	snp	A/T	6.44268e-05	0.00567532	missense, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573722	TTGAGGAGTTTGTTG[A/T]CCAGGATGCTGGACT	84708
rs760134066	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53630837	TTGCTAATTCAGTGT[C/T]TGCAGTGATTTTAAA	84708
rs760139655	in-del	-/C	0.000138699	0.00832647	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507960	GCCAAGGAGCCCATT[-/C]CCGGACAACCACCCA	84708
rs760151267	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53474635	ACCATGTTTATTCTG[C/T]TACTACAGGGAGAGG	84708
rs760152334	snp	A/C			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53515408	ACCACCCTGATAATG[A/C]ATAATTACTTGTGGT	84708
rs760156506	in-del	-/T			intron-variant	LNX1	GRCh38.p7	4:53626389	CTTTAAAAGGGTAAA[-/T]TTTAGGTATGTGAAT	84708
rs760157580	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53491932	AGCTGGGATCACAGG[A/C]GTGCGCCCCCACCCC	84708
rs760165331	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53589364	TTTTTCCAAACTGTT[A/T]ACATTGCAGTTAATT	84708
rs760179311	snp	A/G	1.64795e-05	0.00287045	synonymous-codon, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498803	GATCTTGATGCTGGT[A/G]ATTTCACCATCTGGA	84708
rs760186496	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53618952	ATACAGGGTCTTGCT[A/G]TGTTACGCAGGGTGG	84708
rs760186968	in-del	-/C	1.65121e-05	0.00287329	frameshift-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460952	GTTAGAGTAATTCTT[-/C]CCTTTAAGTTCTTTC	84708
rs760194239	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53477949	GGACTTTTAAATGGC[A/G]TAATTCCTCACCCAT	84708
rs760198960	in-del	-/A			intron-variant	LNX1	GRCh38.p7	4:53644916	ACAAGTAGCACAGTC[-/A]AAAATGCGCTTCTCA	84708
rs760223120	in-del	-/G			intron-variant	LNX1	GRCh38.p7	4:53539901	AACCAGCTGCAATTA[-/G]GATTTCTACTGTCCT	84708
rs760271973	snp	C/T			intron-variant, utr-variant-5-prime	LNX1	GRCh38.p7	4:53558179	GAGAGGATGTAGGAA[C/T]GCAAGGAGCCACCAC	84708
rs760277168	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53527124	AAACATTAGTTACAA[C/G]TGAAATATACTATTG	84708
rs760293300	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53642352	GCTATATTTAAAATG[C/T]ATACATGCTTTTGAA	84708
rs760304041	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53486720	TTAAAACTAAGTAGC[A/G]TCTGTATGGAAGGAC	84708
rs760304079	snp	G/T	1.64868e-05	0.00287109	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507323	TTCATTTACCTTCAG[G/T]GGCAGTGGTGTTTTC	84708
rs760310746	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53641056	GCCTTGGAGGCGACT[C/T]GGCACAGGCTACTGC	84708
rs760315858	snp	A/T			intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498310	AAAAAAAGAGATAAA[A/T]GGAGAAAGAGGAGGT	84708
rs760318994	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53526289	GCTTATGAATGTTGA[C/T]GTAAAATGATGAGTA	84708
rs760320962	snp	A/C	0.000184117	0.00959296	missense	LNX1	GRCh38.p7	4:53481738	GGGAGTGTTGCTCCT[A/C]TCCCCTGGCCCTGGG	84708
rs760338687	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53488001	CAGTGAATCCATCTT[A/G]TGCTCACAAAGCCCT	84708
rs760384306	snp	C/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53601415	CAGCTTTGACAAGTT[C/G]TGCCATGGGTATGCT	84708
rs760398788	in-del	-/TA	5.37014e-05	0.00518149	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461400	TTATGAAACAACATT[-/TA]ATACAAGTATTTTTG	84708
rs760404934	snp	G/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53514365	AGACATACCCAAGAC[G/T]GGGTAATTTATAAAG	84708
rs760427922	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53643374	AGGCTGATCTCAAAC[A/T]CCCGGGCTCAAGTGA	84708
rs760442570	snp	G/T	1.77451e-05	0.00297863	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461416	AATACAAGTATTTTT[G/T]ATTAGTCATTATTAT	84708
rs760444314	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53572631	TCTTACAAAATAATT[A/G]TGGTATGATTGTTCA	84708
rs760445171	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53548064	TTGGGGGTGGTGGGC[C/T]TCAGAGAAAGCTGGA	84708
rs760446071	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53553646	CAAAAAGAATGTTCA[C/T]GGAGGTCTGCGGATG	84708
rs760544969	snp	A/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53595470	GGTAATTTCTTATGC[A/G]TGACAATGGTTTTCA	84708
rs760569702	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53606554	AAGAAGAGCTGGTAC[C/T]ACTCCTACTGAAACT	84708
rs760572564	snp	A/T	0.000923118	0.0214641	intron-variant	LNX1	GRCh38.p7	4:53481875	CAAGAAGACACAGGC[A/T]TTAGCCACTGTCAGT	84708
rs760592657	snp	A/T	4.98351e-05	0.0049915	synonymous-codon, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461521	GTATTCTTCATAACC[A/T]CCTACAATGCAGAAG	84708
rs760614309	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53615693	TACAACCATGCCTTA[C/T]TAATACAGAGCCTTG	84708
rs760621564	snp	A/C			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53594277	AGCTTATCAAATCAA[A/C]CCCAAGATGGAAGGC	84708
rs760622225	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519256	CCTTTTCTAGAGAAA[A/G]CACCTTAGTCCAGGC	84708
rs760632328	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53543075	TATGTTGCTCAGGCT[G/T]GTCTCAAACTCCTGA	84708
rs760634604	snp	A/G	1.6585e-05	0.00287962	missense, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498661	GAATGATGTCTCCTG[A/G]CAGTAGCCGGCCGTC	84708
rs760654193	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53479077	ATATTTCTAAAATAT[C/T]TTCATAGAGAAAAAG	84708
rs760699467	in-del	-/T			intron-variant	LNX1	GRCh38.p7	4:53638473	TCAAAGCAGCGAAAC[-/T]TTTAAGTCATGGGAT	84708
rs760701811	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53629774	GTCACCTGGAAAATG[C/T]GGAGGCCAACACCCC	84708
rs760705515	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53489066	TCAGAGCAAATCTGG[G/T]CTGTATTAATTTGTT	84708
rs760712970	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53627924	CTCTGGGTCAAGTGG[A/G]CCCTGGATTTACATC	84708
rs760721605	snp	C/T	3.30344e-05	0.004064	missense	LNX1	GRCh38.p7	4:53478735	CAAGTAATTGTAGGA[C/T]GGAGGGGCTGAAGGC	84708
rs760729890	in-del	-/A	1.65696e-05	0.00287828	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508232	CACCTTTACAGCTGT[-/A]ACAGAACCAGCGGGG	84708
rs760760942	in-del	-/TT			intron-variant	LNX1	GRCh38.p7	4:53465806	TGAAACATAGTACCC[-/TT]TTTTTACCACAGATT	84708
rs760772809	snp	A/C			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53597367	TCAAACTTTATCCAT[A/C]TCTCTGATCCTTTGC	84708
rs760777739	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53615777	TAAAAAATTTTTAGT[A/G]GGCATATAGTAGGTG	84708
rs760782844	snp	A/G	1.72806e-05	0.00293938	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507964	AGGAGCCCATTCCCG[A/G]ACAACCACCCATTTG	84708
rs760807850	in-del	-/ATTA			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53500792	AACTACTTTGGTTAT[-/ATTA]ATTAAGTAGGCTATA	84708
rs760817052	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53510532	AGGTTTTACTGTACC[A/G]ATTAGCTGCGTTGGC	84708
rs760818422	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53539297	GAATAGTGAAGTATA[C/T]AGATATTTACCTACT	84708
rs760819071	snp	A/C			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53522783	GCCTGGGCAACAGAG[A/C]AGGGCCCTGTCTCAA	84708
rs760823923	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53586260	CTCATGTATTCATGC[A/G]AGTATGCAGGAGCCT	84708
rs760827624	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53524813	CTCTGCTTTCCAAGA[A/G]GCATGCTAGCAGGAG	84708
rs760829324	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53549107	AATAATATGTGCAAA[A/C]CCCCATGACATGTAT	84708
rs760845351	snp	A/C			intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53499549	CTGCATATATCTCTG[A/C]ATGCAGAGGCCTTCA	84708
rs760895753	in-del	-/ATT			intron-variant	LNX1	GRCh38.p7	4:53551350	CTCTCTAAAATAATC[-/ATT]GGTTGAAGCCAGGGC	84708
rs760901478	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53579451	CATCTCTTTTTGGTC[C/T]TAATCCCTGCTTCCT	84708
rs760908280	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53540630	GAGGTTGCAGCGAGC[C/T]GAGATTGCGCCACTG	84708
rs760908342	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53528732	GAGAACAGATAATTG[A/G]CCAAAGCTGGCCTAA	84708
rs760923199	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53465458	GTTTGGCTGACATCA[C/T]GGCAAAATTTTCTGA	84708
rs760931183	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53635315	CTAGATCCCCCCTTC[C/T]GGATGTGCCTGTTTT	84708
rs760966835	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53648081	GGAGTACAAATATAT[A/G]TTTGAGTCCCTACTT	84708
rs761021736	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53547170	GATAACCAAGAAAGA[C/T]AGACACTGCAAATTA	84708
rs761022595	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53536985	CAGTGATGATTTCTA[A/G]TTACTTAGGAAAATC	84708
rs761042906	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53531779	ATTTTTCTTGACATC[A/G]GATCATAATTGCTGC	84708
rs761054761	snp	C/T	1.67058e-05	0.00289009	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508057	TCTGCCGAGGACACG[C/T]AGGCAGGGTTGTCTA	84708
rs761056848	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53482959	CTATGTACATTGATA[C/T]TTGGACAGGCATTCA	84708
rs761083062	snp	G/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53521814	AGGCTTACTCTTTGG[G/T]TACTGCTCTGCTGGA	84708
rs761095874	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53561525	GCCACTGTGCCTGGC[C/T]CTCCGTGTATTTTTT	84708
rs761100567	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53609029	ACAAGGCTACAATAA[C/G]CAAAACAGCGTGGTA	84708
rs761137937	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53475518	AAACTCATTTGAAAT[A/G]TAAAAAGAGAGAGAG	84708
rs761142910	in-del	-/ACAC/ACACACACACACACACACAC			intron-variant	LNX1	GRCh38.p7	4:53529106	AGTCCTGACCAACAC[-/ACAC/ACACACACACACACACACAC]ACACACACACACACA	84708
rs761148826	in-del	-/AAAT			utr-variant-3-prime, downstream-variant-500B	LNX1, FIP1L1	GRCh38.p7	4:53460357	ATCGGTGATGGTAAC[-/AAAT]AAATAACATGGTATT	84708
rs761193472	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53580044	CACTTTAACCTTGTC[A/G]AAGATGAAACACTAT	84708
rs761194906	snp	A/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53511457	ACTCTCAGATGGTGA[A/T]GGGTGATGGCCATGA	84708
rs761199841	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53544501	GTCCGGCCTGAGAGG[C/T]GCTGATTTCTTTTGT	84708
rs761201223	snp	C/G	1.6476e-05	0.00287014	synonymous-codon	LNX1	GRCh38.p7	4:53476785	CATGACCCAGGATGG[C/G]GACCAGTCACTGGGT	84708
rs761223139	snp	C/T			upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53591760	AGCACGTGTCCAGCC[C/T]CGTGTTCAGATCTGA	84708
rs761253950	snp	A/G	8.23811e-05	0.00641746	synonymous-codon	LNX1	GRCh38.p7	4:53496266	TCTGTAGGCATCCGG[A/G]GCCTGTCCATTGTTC	84708
rs761258146	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53503862	CTGTTGGCTGAGTGC[A/G]GTGGCTCACACCTGT	84708
rs761274644	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53493112	GTAGCTGGAATTACA[C/G]GTGCCTGCCACCACA	84708
rs761278313	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53505084	TTCAATTTGTAAAAA[C/T]AAAAATGAGGTATGC	84708
rs761278908	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53473877	AACACTAAATATATG[A/G]AATATAAAATATATC	84708
rs761279070	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53497727	CACAGTGTAGCTGAT[A/T]GTACTGCGGCCTGCC	84708
rs761292976	snp	C/G/T	3.29469e-05	0.00405864	missense	LNX1	GRCh38.p7	4:53476865	CCTGGGGCTCATACT[C/G/T]TTTGACTTCCAAAGC	84708
rs761296183	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53647319	TAAGCATAATGCAGA[A/G]TGTCTCTTTTATTTC	84708
rs761296679	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53533049	GTTATTAAGCACATA[C/T]GCTCCCTAGGTGCAG	84708
rs761307697	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53580198	AAAATTTTCCTTTCC[C/T]ATACCTCACCTGCCC	84708
rs761333749	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53621042	CTGGCTTTTGCTGAG[A/G]TTCCCACCTTCACCT	84708
rs761349656	snp	C/T	2.27291e-05	0.00337106	synonymous-codon, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573697	GAATGGGCAGGTCAC[C/T]AGTAGCTTGTTGAGG	84708
rs761360674	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53581275	GATCATTAAGGAAGT[C/T]GAAAAATGTGGAAAA	84708
rs761379580	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53554953	TGGATTAGTTCCAGC[A/G]TCTGAGCTGGGCATG	84708
rs761387444	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53642956	GGTTCTCTGTGTGGG[A/G]TGATTTTGCCCTCCA	84708
rs761439218	snp	C/G	1.64855e-05	0.00287097	missense	LNX1	GRCh38.p7	4:53476756	GTTTGGACTTACCGT[C/G]GTAATTCCAGCCACA	84708
rs761451479	snp	C/T	0.000318827	0.0126219	synonymous-codon, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573640	GGTTTGAAAGTGATG[C/T]TCGAGGTCACAGCGC	84708
rs761474282	snp	C/T	3.29544e-05	0.00405908	missense, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498781	TTTCACTGGGATCTA[C/T]TCGATTGATCTTGAT	84708
rs761498654	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53542864	TCCCATCAGGAATAA[A/T]TCAGGGGGAAAGCAA	84708
rs761511132	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53572777	CACCAGAATTCTGCC[A/G]CCAGTGTGGGTGTGT	84708
rs761530709	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53627524	TCAACCACAGATCAA[C/T]AAAACAAGATTTTCT	84708
rs761539112	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53590434	TTTTCCAGCTCATCC[A/C]AGCAGGCAGCTGGGC	84708
rs761575421	in-del	-/GTTTG			intron-variant	LNX1	GRCh38.p7	4:53491801	ACGATACTTTTTTTT[-/GTTTG]TTTGTTTTTTGAGAA	84708
rs761600476	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53585817	AGCCTCCAGAACTGT[A/G]AGACAATAAATGGGA	84708
rs761613339	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53549210	TAAAGCTTCTGGGCA[A/T]CAAGGTCATAAAAGA	84708
rs761663239	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53527332	GACTTTCTTCTATTT[A/T]AGGAATTTATATACT	84708
rs761673380	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53614333	TCTAAGACTTCCCCT[C/G]CCATGACACACCATT	84708
rs761686192	in-del	-/T			intron-variant	LNX1	GRCh38.p7	4:53484581	AAAAGAAAAAAAAAA[-/T]CTTTAGTAAAAACCA	84708
rs761688492	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53651707	CTCAACCTCTTTATC[C/T]ATGGGTAAAACTGCA	84708
rs761690234	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53536899	AGTATAGATGTAGAA[C/T]TTCTGCTCCAACCCC	84708
rs761706942	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53540899	CCCAGCACTTTGGGA[A/G]GCTGAGACGGGCGGA	84708
rs761745567	in-del	-/T/TTTTTT/TTTTTTTTTTT			intron-variant	LNX1	GRCh38.p7	4:53495548	AATGCATGGCATAGC[-/T/TTTTTT/TTTTTTTTTTT]TTTTTTTTTTTTTAA	84708
rs761745938	snp	C/T	1.66815e-05	0.00288799	missense	LNX1	GRCh38.p7	4:53481802	TGAAAGATGTCAGGG[C/T]TCCGCTGCCGAACCT	84708
rs761756542	snp	A/G	6.60502e-05	0.00574637	intron-variant, missense	LNX1	GRCh38.p7	4:53557958	ACCAGCAACAGAAGC[A/G]CCTTCATTCTCCGAG	84708
rs761777197	snp	G/T	3.30666e-05	0.00406598	missense, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460993	CCAAGCAAGCATGTA[G/T]CATTCCTGATGTACT	84708
rs761779646	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53625115	GTAAGAGCAAAAGCT[A/G]TGAAACTCTTGGGAA	84708
rs761809402	snp	C/G	4.91075e-05	0.00495493	intron-variant	LNX1	GRCh38.p7	4:53496425	ACAATCGTGCGGTCA[C/G]CTCCACCTGCCACAA	84708
rs761869183	snp	A/G	5.36495e-05	0.00517898	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461402	ATGAAACAACATTTA[A/G]TACAAGTATTTTTGA	84708
rs761893141	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53540640	CGAGCCGAGATTGCG[C/T]CACTGCACTCCAGCC	84708
rs761909300	snp	C/G	1.67548e-05	0.00289432	missense	LNX1	GRCh38.p7	4:53496355	GCAGGAGACGCACAG[C/G]GTAGTTGTGAGGGAC	84708
rs761959739	snp	C/T			intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53499630	GAATTGCAGTTTTAT[C/T]GCTTGCTTATTGAGA	84708
rs761967070	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53489882	ATTCCAGATTAAGTG[A/T]ACTGATCTGTTAAAA	84708
rs761968423	snp	C/T			intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53558911	CTTTAAGATCTGGGA[C/T]TTGAGACTGCATCAC	84708
rs761995213	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53490837	ATAAAATCCACTCTT[C/T]AGAAACGGCATGCGA	84708
rs762022988	snp	A/G			intron-variant	LNX1, LOC101928879	GRCh38.p7	4:53575446	CCAACTCTGAGCTAG[A/G]TCATGAGTTTGATAT	84708
rs762032277	snp	A/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53598818	CATTTAATTTTCACA[A/G]TAATTCACAATAATG	84708
rs762040914	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53517749	CACTGAATTACATGG[C/T]TGCTCACATAGCTAC	84708
rs762043146	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53530432	ATTTATAATTAAAGA[A/C]GTGCAACATTATACT	84708
rs762060862	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53486938	AAGCCTCATTTATAT[A/G]TACCCATCTTTAAAT	84708
rs762093600	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53551743	GGCCCTCTTCTAAGT[A/G]TACTTCCTTTTGTTC	84708
rs762136193	in-del	-/A			intron-variant	LNX1	GRCh38.p7	4:53540240	ATACAAAAATTAGCC[-/A]GGCATGGGGGCGTGC	84708
rs762154699	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53563750	ATTTTGGTCAGGCTG[C/G]TCTTGAACTCCTGAC	84708
rs762217955	in-del	-/AA			intron-variant	LNX1	GRCh38.p7	4:53610717	CCGTCTCAAAGAGGA[-/AA]AAAAAAAAAAAAAAA	84708
rs762226344	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53494572	AAAAATCTCCCCTGC[A/G]CCTGCATCAGCATCA	84708
rs762238481	in-del	-/TATG			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53594154	TAATATATATATATA[-/TATG]TATATATAAATATGT	84708
rs762240570	in-del	-/A			intron-variant	LNX1	GRCh38.p7	4:53528076	TCCAGTCTGTCTCCT[-/A]AAAATTCTTTGTAAT	84708
rs762246202	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53539519	TACAGGCATGTGCCA[C/T]CATGCCCAGCTAATT	84708
rs762261458	snp	G/T	1.77792e-05	0.00298149	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461641	TTTAAGTTTCACAGT[G/T]AAGGGAATACTTACT	84708
rs762268317	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53627390	AAGTGTTGGTAAACT[C/G]ATTCTAACAGGGTTG	84708
rs762269969	snp	C/T	3.46795e-05	0.00416396	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507958	AAGCCAAGGAGCCCA[C/T]TCCCGGACAACCACC	84708
rs762304959	snp	A/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53599381	GTTTATAAATGCCAC[A/G]GCAACATCAGGAAGT	84708
rs762328480	in-del	-/T			intron-variant	LNX1	GRCh38.p7	4:53590516	ATTGGGCTGTCAAGA[-/T]ACAGGCTGTGTGATC	84708
rs762338879	snp	A/G	1.78166e-05	0.00298462	intron-variant	LNX1	GRCh38.p7	4:53495979	TGCATTCTTGCTCAT[A/G]TCCGGGGTTTCTGAC	84708
rs762343012	in-del	-/AG			intron-variant	LNX1	GRCh38.p7	4:53486901	TCCATACAGTGACTA[-/AG]AGAAGAAAAACATAG	84708
rs762348787	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53562867	ATACATATTTTAAAA[C/T]ATCATATTGTACACC	84708
rs762401059	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53648221	CTACATTTCCATCAA[C/G]AGTGCACAAGCATTC	84708
rs762412404	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53495405	CTTGCCTGAGTGATC[A/G]AGAATTTGCGTCCCT	84708
rs762446017	snp	G/T	1.64735e-05	0.00286993	synonymous-codon	LNX1	GRCh38.p7	4:53496188	CTTGCGCACCAGTTT[G/T]ATTCCAAGCTGCTCC	84708
rs762485003	snp	C/T	1.68001e-05	0.00289823	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507496	CGACAGGAGGAACAG[C/T]AGTTATGATTTAATA	84708
rs762498599	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53626021	AATGAATAAATAAAA[C/T]GTTGAATATTCATGT	84708
rs762501682	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53494530	CAAGATCTTCCTCCT[C/G]TGAGGAATTCACAGG	84708
rs762528457	snp	G/T	5.20974e-05	0.00510352	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461626	CAGTGTACATGCATA[G/T]TTAAGTTTCACAGTT	84708
rs762528691	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53505530	GTGCTGGGATTACAG[A/G]AGTAAGCCACCACGT	84708
rs762551077	in-del	-/GTC			intron-variant, utr-variant-3-prime, downstream-variant-500B	LNX1, FIP1L1	GRCh38.p7	4:53459869	TTGAGATTAAAACTA[-/GTC]GTCTTTATCATTACT	84708
rs762576069	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53649356	AGGCGACTACTATTA[C/T]AATCTCTAGTTTTAC	84708
rs762583139	snp	A/G	1.64846e-05	0.0028709	synonymous-codon	LNX1	GRCh38.p7	4:53496074	TCGAAGATCATGTCC[A/G]TTGATGGCTAACACA	84708
rs762608235	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53475957	AACATCTTAGCAAAG[A/G]CGAAGTGCTCTGGGG	84708
rs762608313	snp	A/G	3.42108e-05	0.00413573	intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573613	ACCGGCTCGCTGATG[A/G]GGGACCTACCTGGTT	84708
rs762615700	in-del	-/ACAACG			intron-variant	LNX1	GRCh38.p7	4:53583970	ACAACAACAACAACA[-/ACAACG]ACAAATGAAGGCAGA	84708
rs762619354	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53506430	ATTGGGGAAAACATA[C/T]GGGATCTAAGACTCA	84708
rs762620996	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53523359	TGGCATGGTCTCAGC[C/T]CACTGCAACCTCTGC	84708
rs762636435	snp	C/T	1.67629e-05	0.00289503	intron-variant, utr-variant-5-prime	LNX1	GRCh38.p7	4:53557986	GAGCAGTGTGCTGCC[C/T]TCTCCCTGGCCACCT	84708
rs762664250	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53622540	GACCATTATCTCCAA[A/T]TTTGACATCTGAAGA	84708
rs762666621	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53647644	CTTGCCATCTTAACA[A/G]TTTTTAAGAGTACAG	84708
rs762685469	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53581326	AAACTTAAAACATCA[A/G]TTTAAGTTTAAATAT	84708
rs762714977	snp	C/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53593684	GGCTTTTTTTTTGGG[C/T]CATTAGGGCTGTTAC	84708
rs762732700	snp	A/C			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53501261	CTTCACAATAACCCT[A/C]TGAAATAGATGATAA	84708
rs762747036	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53539038	TGGTCCCCCTGAAAG[C/T]GAAGTCAGTTCCAAG	84708
rs762753152	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53627172	AATGGTGGTTTCAGG[A/G]AGAAGGAAAGCGTAG	84708
rs762770695	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53632087	AGGGAGGTGGGTCAT[C/T]GAAGGGAGCAGAATG	84708
rs762792338	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53589632	ATCTCCCATCTTACC[A/G]ATGAAGAAACTGAAA	84708
rs762794767	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53489492	TGAGTCAGTAAAATG[A/G]CTCAGCATCCTTGCC	84708
rs762802529	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53615400	AGGTATTCAAGAGGC[C/T]TCGCAGCTTCCACCC	84708
rs762808291	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53482484	CTGATAGGTAGATAA[A/G]GAAAATGTGGTATGT	84708
rs762826524	snp	A/T			nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53603914	TCTGTTCTGATAGGT[A/T]GGTGCCTCTACTGAT	84708
rs762846749	snp	C/T	1.65362e-05	0.00287538	missense, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498673	CTGGCAGTAGCCGGC[C/T]GTCTCTGGCGATCAC	84708
rs762849769	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53643214	GGAGTGCAATGGCAC[A/G]ATCATGGCTCACTGC	84708
rs762860950	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53478889	CATAAATACAATGGT[A/G]GTTCTTGAAATCACA	84708
rs762879314	snp	A/G			nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53604810	AGCCTCTTGGGTGGG[A/G]AAGACAGGTCACAGG	84708
rs762885815	snp	C/T			intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53574586	ATAGTGCTGTTGAGC[C/T]TTTCATATTTTCACT	84708
rs762898352	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53614716	CCTTTGGTCAGCCTA[C/T]GCTGTTTATGGCTCA	84708
rs762911499	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519802	TCCCCAGTTTGCAAA[C/T]GCGGGAACTTAATAC	84708
rs762931668	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53544671	TTTCTAAAGAAAAAA[A/G]TGTGCAGGGGGCGAA	84708
rs762969714	snp	C/G/T	3.2986e-05	0.00406105	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508180	CAGCCATCTTGTGAG[C/G/T]GCCTCTTCCTATCTT	84708
rs762970381	snp	A/G	1.64768e-05	0.00287021	missense, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498760	CCACCAGCCTAATAG[A/G]GAGGCTTTCACTGGG	84708
rs762976702	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53613216	ACATAACTGTACACA[C/T]GAACATATGTTTAAA	84708
rs762992650	snp	A/G			upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53592036	AAACAATTTGAAATA[A/G]GATACCTGTCAGCAG	84708
rs762997215	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53488970	CTCCCACTGAGCAAC[A/G]AGTTGGAGGCTCCAG	84708
rs763004151	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53607970	CAAAAATCAGCTCAA[G/T]ATGAATTAAGAACTT	84708
rs763024805	snp	A/T	1.64819e-05	0.00287066	missense	LNX1	GRCh38.p7	4:53496280	GGGCCTGTCCATTGT[A/T]CCTGCTGCGGAACTT	84708
rs763034633	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53530500	AGCGATGATAACATC[C/T]ATTGCATATAAAGAT	84708
rs763035782	snp	A/G			upstream-variant-2KB	LNX1	GRCh38.p7	4:53653085	ATTTATTAAGTGCTT[A/G]CCGTCTACCAGGTTC	84708
rs763056436	snp	C/T			upstream-variant-2KB	LNX1	GRCh38.p7	4:53654363	TCATCTGCTTCGTGG[C/T]TTTTCACCAACAGGA	84708
rs763056460	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53629913	CACAATAAAGACAAC[A/G]ATACATCAATTCTTC	84708
rs763057241	snp	A/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53596110	TGGCTAATTATATGT[A/G]CTTAGCATAACGCAG	84708
rs763088617	in-del	-/AA			intron-variant	LNX1	GRCh38.p7	4:53541136	GCGAGACTCTAACTC[-/AA]AAAAAAAAAAGAAAA	84708
rs763096053	in-del	-/A			intron-variant	LNX1	GRCh38.p7	4:53472276	TCACTCATAGGTGGG[-/A]AATTGAACAATGAGA	84708
rs763100591	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53548177	GGATGTCTGCTTCCT[C/T]GGCCTGCCAAGTTTT	84708
rs763134982	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53543543	GAAAAAAAAATCACA[C/G]TATACAAAGAAAACG	84708
rs763139344	in-del	-/CTTTCTTTTCTTT			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53594693	TCTTTTACTTTCTTA[-/CTTTCTTTTCTTT]CTTTCTTTTTTAATT	84708
rs763147704	snp	C/T	1.66852e-05	0.0028883	synonymous-codon	LNX1	GRCh38.p7	4:53496350	CTGCCGCAGGAGACG[C/T]ACAGCGTAGTTGTGA	84708
rs763153349	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53520459	GCCAGAATCGTTTGT[C/T]CATTCTGTGAGTCTC	84708
rs763162307	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53606669	AAAAGAAAACTTCAG[A/G]CCAATATCTTTGATG	84708
rs763166059	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53479473	TATGGCATGTGTGCA[C/T]GTGTCCTGTCTCATG	84708
rs763167607	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53510071	AAAGGGACAAGCAAA[C/T]GTTTTATCTGCTTAG	84708
rs763183281	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507971	CATTCCCGGACAACC[A/G]CCCATTTGACTCACC	84708
rs763200159	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53629284	CTCCAGCCACCCCTG[C/G]GTGCATCCAGGAACT	84708
rs763239643	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53619538	ATGTTAGAGAAAAAA[G/T]TACTGCCTTCCTTTT	84708
rs763241083	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53617880	ATGACAGAAATTGAG[C/T]CAGTTTTCTCCATAT	84708
rs763270316	snp	C/T	1.70041e-05	0.00291577	intron-variant	LNX1	GRCh38.p7	4:53478515	ACAAGCTACTAATTT[C/T]TCTTGATTCTCTGCC	84708
rs763287945	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53553289	ACTGTAGTGCCCATA[C/T]GGATCCCCTGGGGAG	84708
rs763288143	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53540958	CCTGGCCAACATGGT[A/G]AAACCCTGTCTCTTC	84708
rs763295429	in-del	-/TTT	1.66396e-05	0.00288436	cds-indel	LNX1, FIP1L1	GRCh38.p7	4:53461479	TCCTTCAACAATGGA[-/TTT]GATGAAAAAAGGTTT	84708
rs763296441	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53578879	GAGATAATTGACTGA[A/G]CAAGCAGTTTTGGCT	84708
rs763311148	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53511498	TGAATACAAGGAACA[C/T]AGAAAACCCCTTTTC	84708
rs763325085	snp	C/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53598604	CTTTCCACGTACTCT[C/T]AGGACTTAGCCTGGT	84708
rs763347762	snp	A/T	3.2975e-05	0.00406035	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507419	CACTCAAAGCTCGAT[A/T]TATTTTTTTAAATGA	84708
rs763352478	snp	A/T	1.71781e-05	0.00293066	missense, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573876	AAGCCTGCAGGCAGA[A/T]GTGGCAGATGAGGTC	84708
rs763357358	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53532556	ACCCTGCAAAAGGCC[A/T]TTCCCTCTTGAATGG	84708
rs763401807	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53588373	CATTTCAACCCATTT[A/C]ATCTTCATGATAACC	84708
rs763409358	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53612107	CAGAAAAGCACATAC[A/G]AAGGGTTGAGAAACT	84708
rs763457066	snp	A/G			intron-variant, utr-variant-3-prime	LNX1, LOC101928879	GRCh38.p7	4:53577495	TGTGCTGTGGAAGGC[A/G]TCAGATACTTCCAGA	84708
rs763488982	snp	A/C/G			intron-variant	LNX1	GRCh38.p7	4:53552168	GTCACGCAGCTAGTG[A/C/G]CACCAGTTTCCAGGA	84708
rs763489686	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53650219	ACAAATGCATAGCGC[A/G]TGTCACAGTCCTTAA	84708
rs763500009	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53551956	ATTGCTCATTTTAAT[A/C]TCTGGAGTACAAAAC	84708
rs763509163	snp	G/T	1.64806e-05	0.00287054	missense	LNX1	GRCh38.p7	4:53496081	TCATGTCCATTGATG[G/T]CTAACACACGGTCAT	84708
rs763525664	snp	C/T	1.76852e-05	0.0029736	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461637	CATATTTAAGTTTCA[C/T]AGTTAAGGGAATACT	84708
rs763529044	snp	C/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53599637	GTCTGGATCGGGACC[C/T]CTTTCCTGTAACAGT	84708
rs763604835	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53543696	ATTCCCTGCCTTTGC[C/T]AAATGGTAAACAAAT	84708
rs763608857	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53630902	CATCAGCTTTTAGAA[C/T]TTGGGAAGGGGAACT	84708
rs763612909	in-del	-/TTT/TTTT			intron-variant	LNX1	GRCh38.p7	4:53563537	GTTAGCTTCAAATTC[-/TTT/TTTT]TTTTTTTTTTTTTTT	84708
rs763615989	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53640765	TTAGGTCTGGAGGGC[C/T]TTTGAAGGCAGTTTC	84708
rs763616220	snp	G/T	0.000101225	0.00711352	intron-variant, utr-variant-5-prime	LNX1	GRCh38.p7	4:53557995	GCTGCCTTCTCCCTG[G/T]CCACCTTCTGTCAGC	84708
rs763622638	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53629908	GTATGCACAATAAAG[A/G]CAACAATACATCAAT	84708
rs763650139	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53494674	CCACACTGGAGGATC[A/C]TTTGGAAGAATAATC	84708
rs763666140	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53619775	TATGTTTAATTTTTC[A/G]ATGAACTGTCAAACT	84708
rs763692898	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53473320	ATAATATTGAAAACA[C/G]AGTGAGCATTGAAGG	84708
rs763703547	snp	G/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53515950	TTATTTACCATGAGG[G/T]TTAAAGATTCGCACA	84708
rs763704519	in-del	-/G	1.77439e-05	0.00297853	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461415	AATACAAGTATTTTT[-/G]GATTAGTCATTATTA	84708
rs763774500	in-del	-/C			intron-variant	LNX1	GRCh38.p7	4:53626558	ATTTTGAAAAGATCA[-/C]CTGGCTTCAGTGTAG	84708
rs763811206	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53613472	GGTATTAAGCCTAGT[A/G]TCCATATTTGTTATT	84708
rs763818225	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53582348	AGGCAAGAGGAATGA[C/T]TCGCTTCAAAGAAGC	84708
rs763819252	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53526341	CAGCTACTTCTGAAT[C/G]GTTTTCATAATCTTG	84708
rs763822583	snp	G/T	9.37925e-05	0.00684744	synonymous-codon, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573625	ATGGGGGACCTACCT[G/T]GTTTGAAAGTGATGC	84708
rs763824656	in-del	-/G			intron-variant	LNX1	GRCh38.p7	4:53540617	AACCCAGGAGGGGGA[-/G]GTTGCAGCGAGCCGA	84708
rs763853431	snp	A/C	1.65605e-05	0.0028775	intron-variant	LNX1	GRCh38.p7	4:53496441	CTCCACCTGCCACAA[A/C]CCTTCCTGAAAGATC	84708
rs763859103	snp	C/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53602253	CAACAGATGCCAAGA[C/T]GAAATTAAATATGCA	84708
rs763868250	snp	G/T			intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53462513	ATATGGCTATTTTGT[G/T]TATATACCGTACCTT	84708
rs763890406	in-del	-/T			intron-variant	LNX1	GRCh38.p7	4:53640048	CTCAAAAAAAAATAA[-/T]AAATAAAAAAGAATT	84708
rs763915956	in-del	-/C			intron-variant	LNX1	GRCh38.p7	4:53472989	TTTTTAATGCACCTT[-/C]TGGAGTGATTTTCAA	84708
rs763926060	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53626031	TAAAATGTTGAATAT[C/T]CATGTAACAGAATGT	84708
rs763930380	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53651029	TCTCATTTTACATAT[C/T]GGCAAGGTGAAGTTA	84708
rs763934113	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53641165	TATGCTGGAGGAGAT[A/C]CAAGCTGCTTGGCCA	84708
rs763938904	snp	A/G	4.98517e-05	0.00499233	missense	LNX1	GRCh38.p7	4:53496340	CCTGGCAGGGCTGCC[A/G]CAGGAGACGCACAGC	84708
rs763941542	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53571756	ACCCTCAACTCCCAG[G/T]CTCAAGCAATCCTCC	84708
rs764003928	in-del	-/TTTGAG			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53515607	TATGATTTTATTTGC[-/TTTGAG]TTTAAGAAGCATTAT	84708
rs764022120	in-del	-/TGTGTA/TGTGTATA/TGTGTGTGTG			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53512510	GTGTGTGTGTGTGTG[-/TGTGTA/TGTGTATA/TGTGTGTGTG]TGTGTGTGCATGCAG	84708
rs764040043	snp	A/G			intron-variant, missense	LNX1, LOC101928879	GRCh38.p7	4:53575620	CTTGGGACCAGGCCC[A/G]CTTTTGGCTGCATTG	84708
rs764042342	in-del	-/T			utr-variant-3-prime, downstream-variant-500B	LNX1, FIP1L1	GRCh38.p7	4:53460324	GAGCATTTTTAGGGA[-/T]TAAGCCTAGGAGGTA	84708
rs764079579	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53536152	TTACATAAGCAGGAA[G/T]AACTGGGTAGACACT	84708
rs764080595	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53479418	AGAGATGTTTAGTTG[G/T]GCACTGAGGGGCTGG	84708
rs764086578	snp	C/T			upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53592357	TGGTTGCTTCACCTT[C/T]TCCAGCAGGAAAGGA	84708
rs764095293	snp	A/G			nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53604144	TTAATCAAATTGATG[A/G]CAATTTGAAGTTGCC	84708
rs764118768	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53557108	AAGCTTACTAACAAA[A/C]GGAGCTGGAAAAATA	84708
rs764142830	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53489743	AAATTTGGAGCCCTA[A/G]ATAAAAATCACTTGG	84708
rs764153655	snp	C/G	1.64822e-05	0.00287068	missense	LNX1	GRCh38.p7	4:53496281	GGCCTGTCCATTGTT[C/G]CTGCTGCGGAACTTC	84708
rs764157446	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53464851	TCAATGATAGCCAAT[C/T]ACAACAATTTGTACT	84708
rs764168308	snp	G/T	1.68165e-05	0.00289965	missense	LNX1	GRCh38.p7	4:53481724	AGAGGCCTCACCTTG[G/T]GAGTGTTGCTCCTCT	84708
rs764174136	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53617097	ATAAACTATAATACA[A/G]AAGCAGCATATAAGA	84708
rs764183960	snp	C/T	1.64754e-05	0.00287009	synonymous-codon	LNX1	GRCh38.p7	4:53476899	GAGTACTATCGAGGA[C/T]GATGTTCTTTTCAAT	84708
rs764203938	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53543617	TTTTTTTTTCAGAAC[A/T]TTAATTTACTTTCAC	84708
rs764204870	snp	A/T	1.67259e-05	0.00289183	synonymous-codon	LNX1	GRCh38.p7	4:53496353	CCGCAGGAGACGCAC[A/T]GCGTAGTTGTGAGGG	84708
rs764209701	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53489080	GTCTGTATTAATTTG[A/T]TTGCCATTGAAACTT	84708
rs764215494	snp	A/C			upstream-variant-2KB	LNX1	GRCh38.p7	4:53653302	CCACTGGTTTGCTTA[A/C]GCACTTCTGTGGGCT	84708
rs764220068	in-del	-/GAA	0.000133543	0.00817028	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508252	AACCAGCGGGGAGGT[-/GAA]GAAGAGCTTTGGCTC	84708
rs764262471	in-del	-/G			intron-variant	LNX1	GRCh38.p7	4:53630093	TCATTAAAAAAAGGT[-/G]GGGGGGGGCATGCGG	84708
rs764278245	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53627283	CTTAATCTCTTTTCA[C/T]GGCCTTTGAAGGTAC	84708
rs764283077	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53610137	TGTTTTTCATATGTC[C/T]GCAGAACATTTATAG	84708
rs764305888	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53466376	AAACCTGAAGACAGC[C/T]GAATAGGAACAGCTC	84708
rs764306292	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53638021	ATAGATGGCAGCCAC[A/G]ATGGTGGCATTTTAA	84708
rs764318678	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53549564	ATTAAAGAATTATGG[C/T]TGTTTTTGGTGTGAT	84708
rs764319081	snp	C/T			intron-variant	LNX1, LOC101928879	GRCh38.p7	4:53575429	TAAATAGTTTTCAAG[C/T]GCCAACTCTGAGCTA	84708
rs764330061	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53476308	ATATAAAAATAAAAT[A/G]AAATAAAGCCACAGA	84708
rs764341600	snp	C/T	3.3923e-05	0.0041183	intron-variant	LNX1	GRCh38.p7	4:53478530	CTCTTGATTCTCTGC[C/T]ACCCCAGTGCCTTTA	84708
rs764348485	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53551250	CAGTAGGTAGTTAGA[C/T]AGACATGAGGCAGGG	84708
rs764350248	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53651977	GAAAAAGATACCTAG[A/G]TATTTCCATCTTTTA	84708
rs764389421	snp	C/T			intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53574949	CCTTTAAGCTTTGTT[C/T]TAATAGGACTCTTTT	84708
rs764415822	in-del	-/T			intron-variant	LNX1	GRCh38.p7	4:53545021	GTGGTACCCAGATGC[-/T]TTTTTTCTATTAAAA	84708
rs764417661	snp	A/G	1.71631e-05	0.00292938	synonymous-codon, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573883	CAGGCAGATGTGGCA[A/G]ATGAGGTCATCATCC	84708
rs764433816	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53509592	GCTGTGAGGTTTGAT[C/T]GACATTAAGTCTTAT	84708
rs764444454	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53652141	TTGTATGAGATTCTA[A/C]CTGGTGGAGGAACCG	84708
rs764459153	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53648179	TTGGTGAACCACCAT[A/G]CCATGTTACACAATA	84708
rs764471025	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53539347	AAAAATGCTCAGATG[C/T]CCTTTAGTTTCTCTT	84708
rs764471203	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53562488	CAATCAATGATCTAG[C/G]CAGTCATGCATACCT	84708
rs764480110	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53647325	TAATGCAGAGTGTCT[C/G]TTTTATTTCTGCATA	84708
rs764496977	snp	C/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53597124	AAACCATGTTGCCAG[C/G]CTCTTTTTCTACGAG	84708
rs764498362	snp	C/G/T			intron-variant	LNX1	GRCh38.p7	4:53621095	GTGGTGCACAGGGCA[C/G/T]GGTGACATCACCTGG	84708
rs764512763	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53561530	TGTGCCTGGCCCTCC[A/G]TGTATTTTTTCTTTC	84708
rs764514850	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53471464	AAACATCAAAAGCAA[C/T]GGCAACAAAAGCCAA	84708
rs764531870	in-del	-/C			intron-variant	LNX1	GRCh38.p7	4:53616048	CCCTGCTCCTCACCA[-/C]CCCCGTCCTTCCAAG	84708
rs764585656	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53638809	GTGCCCCAGTCAGAA[G/T]GGCTATTACTAAAAA	84708
rs764588897	snp	C/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53595552	CTCTTTAGGAGCAAG[C/G]CTCTTTTGCAGTCAA	84708
rs764593346	snp	A/T	1.65029e-05	0.00287248	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507434	TTATTTTTTTAAATG[A/T]TCTGCTTCTAATAGT	84708
rs764610439	in-del	-/A			intron-variant	LNX1	GRCh38.p7	4:53473640	GTGACAACAGACACC[-/A]AGGGCCTACTTGAGG	84708
rs764631927	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53521056	GGGAAACTGGGCTAT[A/G]GATCAACGGTGCTTT	84708
rs764644433	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53493129	TGCCTGCCACCACAC[C/T]CAGCTAATTTTGTAT	84708
rs764651628	snp	C/T	1.64849e-05	0.00287092	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507415	AGAACACTCAAAGCT[C/T]GATTTATTTTTTTAA	84708
rs764668933	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53530261	TCGTAAGTAAAAAAG[C/T]CTAATGATAATAGAA	84708
rs764671436	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53622491	CAGCTCCCCTTGTTC[A/C]CTCCCTCACTCTCTC	84708
rs764676710	in-del	-/G			frameshift-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461589	TTTACAGTTATACAA[-/G]GCACCTGAAATAGAA	84708
rs764724392	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53552141	ATCATTTCCTGGCTT[C/T]CTGGGAAGTCAGTCA	84708
rs764747875	snp	A/T	5.41345e-05	0.00520234	intron-variant	LNX1	GRCh38.p7	4:53481895	CCACTGTCAGTTTCC[A/T]TCCACTGCATTCAGC	84708
rs764768752	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53621479	ATATAATGGGTGCTC[A/G]GTCAATGTTCATTTA	84708
rs764769577	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53556556	CATCCATTGAGAGAG[G/T]AATGAGCCTTTTCAT	84708
rs764794774	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53505190	TGACAGCACCTAGGC[C/T]GGTGCCTTACATATA	84708
rs764809077	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53494577	TCTCCCCTGCGCCTG[A/C]ATCAGCATCATACTT	84708
rs764871336	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53533890	AGCATCTGTGTTGTT[C/G]ACAAACTCTCCAGGC	84708
rs764882290	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53651937	TATAAAGAGCGCAAA[C/T]GCCCTGAGGCCTTTC	84708
rs764895334	in-del	-/CTGTATTT			intron-variant	LNX1	GRCh38.p7	4:53561221	ATAGGTAATAGTCCC[-/CTGTATTT]CTTTTCTTTTCTTTT	84708
rs764897920	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53648271	ACAACATTGGTTATT[C/T]TGGAATTTTTTTTAA	84708
rs764931475	in-del	-/T			intron-variant	LNX1	GRCh38.p7	4:53643977	CACAGTTGGTGTACA[-/T]TTTTATTAGTCTACA	84708
rs764946487	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53514564	CATGAGAACAGTATG[A/G]GGGAACTGCCCCCAT	84708
rs764953166	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53543993	TCTCTGGGTCTTTTG[C/T]AACTGAAGAAACAAC	84708
rs764983095	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53621148	TTCAGAGGTCACTCC[C/T]GACCTATGGCATCCA	84708
rs764985827	snp	C/T			synonymous-codon	LNX1	GRCh38.p7	4:53478653	TTCTCTATGTGATGC[C/T]CCCCCTGCGACGGTC	84708
rs764988148	snp	A/G	1.64781e-05	0.00287033	intron-variant, synonymous-codon	LNX1	GRCh38.p7	4:53557891	TTCTGAATACAGGAA[A/G]TGCAGGTTGCCCACA	84708
rs764993846	snp	C/T			upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53591854	AAAGGGAAGTTTAAA[C/T]ACCAAAATGAGACAG	84708
rs765009461	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53488963	AAAAATCCTCCCACT[A/G]AGCAACGAGTTGGAG	84708
rs765036759	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53555027	AATCCAGGAGGGTCT[A/G]TGCATCTGGAAAAAC	84708
rs765041569	snp	G/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53515734	TTTTTCAATAAACAC[G/T]CATGGGAGGGTCTTC	84708
rs765042946	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53544648	TGCCCAGTACCATGC[A/G]AGAATCTTTTCTAAA	84708
rs765082289	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53631066	AAAGTACAGTTCTAT[A/G]GACCGCTGGGTCAAT	84708
rs765082446	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53643097	AGGCAGCTGCCCACA[A/G]TAAAGAATTATTCAG	84708
rs765114799	snp	C/T	7.18004e-05	0.00599125	missense	LNX1	GRCh38.p7	4:53496388	TGCTGATGTCCATCC[C/T]GTTGACCTGGGGGCA	84708
rs765143192	snp	A/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53602727	AGGAATGAAAAACAC[A/G]TGTTGGGTGATAGTT	84708
rs765147194	in-del	-/TG			intron-variant	LNX1	GRCh38.p7	4:53652012	CTCCTCAATTTGATG[-/TG]TGTGTGTGAGAGAGA	84708
rs765166085	in-del	-/T			intron-variant	LNX1	GRCh38.p7	4:53473767	TGACATGAGTTTACC[-/T]ATATAACAAACCTGC	84708
rs765168749	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53645170	ACCTAAAAACACTCC[A/G]GGATACACGGTGGCC	84708
rs765180189	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53500983	TGCCAAACCTAAACC[A/G]CTAGAGAATGTTTGA	84708
rs765183255	snp	C/T			intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53558994	AGCCCCCAGGACTCT[C/T]GCTTACCCCATATTC	84708
rs765227384	in-del	-/A			intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498431	TTTATATACAGAGAG[-/A]AAGGGGGGAGAGAGT	84708
rs765228498	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53572785	TTCTGCCACCAGTGT[A/G]GGTGTGTGTGTGTGT	84708
rs765236942	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53521064	GGGCTATGGATCAAC[A/G]GTGCTTTCTATTTCA	84708
rs765249594	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53613492	TATTTGTTATTTTTC[C/T]TGATCCTCTCCGTCC	84708
rs765251107	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53651179	TTGGTGTAAGCAAAT[A/G]TTCACTCAACAAATT	84708
rs765257343	snp	C/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53601578	CAACTGCGTGAGCCT[C/G]GTAGCAAGCCCATTG	84708
rs765288800	snp	C/T	1.66178e-05	0.00288247	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508075	GCAGGGTTGTCTAGG[C/T]CAGGCTCGTCTGTCA	84708
rs765289405	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53479286	AGCATTTCAAAAACA[A/C]TCTGTCATTTATAAA	84708
rs765347447	snp	C/T	4.95954e-05	0.00497948	missense, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460987	GTCTTGCCAAGCAAG[C/T]ATGTATCATTCCTGA	84708
rs765350539	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53485293	AAGGATCCCAGCAGA[A/G]TGTCCATAGGCTTGC	84708
rs765369014	in-del	-/TTTC			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53512415	TAGATCAGACCCATT[-/TTTC]TTTCTCAGTCCTCTA	84708
rs765396827	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53649960	GGAGAACCTAGACAA[A/G]GACTTGACAGAGAAG	84708
rs765400353	snp	C/T	1.64743e-05	0.00287	missense	LNX1	GRCh38.p7	4:53496231	TTGTTGAGAATCACA[C/T]GAAAGCTGTCATCTC	84708
rs765401736	snp	C/G	1.64795e-05	0.00287045	missense	LNX1	GRCh38.p7	4:53496274	CATCCGGGGCCTGTC[C/G]ATTGTTCCTGCTGCG	84708
rs765402328	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53627933	AAGTGGGCCCTGGAT[G/T]TACATCATTCTGACT	84708
rs765407647	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53489939	TTTCACTGGCAATTC[G/T]TACTGGCTCCGGGGG	84708
rs765418996	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507065	ATAATTATTCTTCCT[C/T]ATATGCATAATGGTA	84708
rs765424299	in-del	-/C			intron-variant	LNX1	GRCh38.p7	4:53572310	ATGAGGGAGGTAGGG[-/C]ATCCTAGTTTAAACA	84708
rs765436017	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53617345	GTCACAGCAGTAAAA[C/G]ATGGTTCAATAGGCC	84708
rs765462557	in-del	-/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53505146	ACCCCTTGATGCCAA[-/G]AACTACATTTTATAT	84708
rs765464109	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53539528	GTGCCACCATGCCCA[C/G]CTAATTTTTTTAGTT	84708
rs765479047	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53634981	CAGGTGCACACTACC[A/G]TATACAGCTAATTTT	84708
rs765497451	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53588019	TTTCCATCATTATTA[C/T]ATCCAGATAGTAGCA	84708
rs765500697	snp	A/T			intron-variant, utr-variant-5-prime	LNX1	GRCh38.p7	4:53558116	CAGATTAAGCCACGT[A/T]AATAAATCACGGGCC	84708
rs765515251	snp	C/T	1.64738e-05	0.00286995	missense	LNX1	GRCh38.p7	4:53476882	TTGACTTCCAAAGCT[C/T]TGAGTACTATCGAGG	84708
rs765524940	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53644315	CTGAGGCACGAAAAT[C/T]GCTTGAACCCAGGAG	84708
rs765530683	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53551890	GGTTGCTACAGATTT[C/G]CCACCAGTAACACTT	84708
rs765543354	snp	A/G	1.64754e-05	0.00287009	missense	LNX1	GRCh38.p7	4:53476802	ACCAGTCACTGGGTG[A/G]GGCCATGTTGTGGTT	84708
rs765545563	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53529718	CATAGTAGGACAGAG[C/G]CACATTGGAAAGAAC	84708
rs765546689	in-del	-/ACAC			intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461940	CTTATTGGTGAACAA[-/ACAC]ACTTATGGATGTCAT	84708
rs765593958	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53615919	AACAATCCAATCATA[C/G]TATTCTAGTTATTTT	84708
rs765626337	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53638964	CAGAACTAACATTTG[A/G]CCCAGCAATTCCATT	84708
rs765635720	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53628189	CTCTTCTTGAAAATA[A/G]TCATCAGGAGAAACA	84708
rs765641162	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53615890	CCCCTCAAGCATTTA[A/T]CCTTTTTATTATAAA	84708
rs765654628	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53611229	AGGAATGAAAAAAAA[A/G]GTCTAAAATAGTGAA	84708
rs765666664	in-del	-/CTTT	1.65127e-05	0.00287334	frameshift-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460954	TTAGAGTAATTCTTC[-/CTTT]AAGTTCTTTCAGCAG	84708
rs765677727	in-del	-/GTG			intron-variant	LNX1	GRCh38.p7	4:53636222	TTCAGGGGAGAAGGA[-/GTG]GTGGTGGTGAAAGAG	84708
rs765678836	snp	C/T			upstream-variant-2KB	LNX1	GRCh38.p7	4:53653400	TGGAAACATGAATAA[C/T]TAGTGAATTAAGTAG	84708
rs765701269	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53527230	TTCAATGAACAGATA[C/T]TGTTTTATTTCTACA	84708
rs765714458	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53562904	ATATACAATATGTAT[C/T]TGTCAATTAAAAAAA	84708
rs765720751	in-del	-/CTT			intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53462083	CTTGGAAAAATACCA[-/CTT]CTTTACACCCAGTGC	84708
rs765725534	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53587341	TTTCATGTCAACCCT[A/C]TTCTTTGGGGATAGT	84708
rs765729438	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53528917	GAGTTGAGACCACAC[A/T]TGTCTGGTTGGTGGG	84708
rs765777821	in-del	-/T			intron-variant	LNX1	GRCh38.p7	4:53477697	TATTTCCATTTTCTA[-/T]TTTTTTATCTTCATC	84708
rs765789102	snp	G/T	1.64768e-05	0.00287021	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507346	GTGTTTTCAGAATTT[G/T]CCCTGCCCTGGTCGG	84708
rs765832790	snp	A/C	1.67298e-05	0.00289217	synonymous-codon	LNX1	GRCh38.p7	4:53481741	AGTGTTGCTCCTCTC[A/C]CCTGGCCCTGGGGAC	84708
rs765851667	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53495411	TGAGTGATCAAGAAT[C/T]TGCGTCCCTCTCTTC	84708
rs765857179	snp	G/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53599686	CCATGATTTTCCCAG[G/T]TCCCCCACAGCCTTA	84708
rs765866296	snp	A/G	1.64866e-05	0.00287106	missense, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498822	TCACCATCTGGAATC[A/G]GGTGGTACAACCTTG	84708
rs765869117	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53564008	GTGTTGAGGCCCACG[C/T]CTCCCTGATGTGGGG	84708
rs765873559	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53535584	AAACTCTGCATTAAT[A/G]TCCTCAGAGGTAAAT	84708
rs765890631	snp	C/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53598594	AGGAATGTGACTTTC[C/T]ACGTACTCTCAGGAC	84708
rs765893808	snp	C/T			utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460659	GGGCTTTTTATTGAA[C/T]AGAAAAAATATAAAC	84708
rs765917569	snp	A/G	1.64863e-05	0.00287104	synonymous-codon, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507324	TCATTTACCTTCAGG[A/G]GCAGTGGTGTTTTCA	84708
rs765923116	snp	A/C			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53523361	GCATGGTCTCAGCTC[A/C]CTGCAACCTCTGCCT	84708
rs765927170	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53639102	GCCAATCAATGGTGA[C/T]TGGATAAAGAAAATA	84708
rs765936708	snp	A/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53598679	GAACTAAAGATGAAT[A/G]TAAGTCAAGGGAAGG	84708
rs765952510	in-del	-/GACA			intron-variant	LNX1	GRCh38.p7	4:53529123	ACACACACACACACA[-/GACA]CACACACACACAAAC	84708
rs765976923	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53494749	TAAGCAGCAGAACTT[A/T]ACAGATATTTGCTGG	84708
rs765977289	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53648410	TTTATATATCTTCTT[A/T]GGAGAAATGTCCATG	84708
rs765982655	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53620606	ATGGGTACAACGTGC[A/G]TTGCTCCACTGATGG	84708
rs765991409	snp	C/T	1.65542e-05	0.00287695	missense, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461016	GATGTACTTCTACCA[C/T]TGACAGCAAGAAGAA	84708
rs766005292	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53622591	GGAAGTTTTTCCAAA[C/T]TGGTATAAAAAACGC	84708
rs766040347	in-del	-/AGAG			intron-variant, utr-variant-3-prime, downstream-variant-500B	LNX1, FIP1L1	GRCh38.p7	4:53459911	TTGCTTAGTATATTA[-/AGAG]AGAGACTCATACATT	84708
rs766050339	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53555801	GGCAAAGTATGATTC[C/T]CTAGCATCATACTTT	84708
rs766063938	snp	A/G			intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498330	AAAGAGGAGGTGGAG[A/G]AAGGGAATGAAGAGG	84708
rs766096153	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53633441	TTTTTACAGTGTTTT[C/T]CACTTCTTCTGGCCA	84708
rs766097670	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53533272	AACATACAAAGGAAC[C/T]AGATTTGCCCGAGGA	84708
rs766147944	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53544920	CTAACTCTGGAGTCC[C/T]GCTTGTGATCATAAT	84708
rs766160972	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53504264	AGCATCTGCTGCTTC[A/G]CTACAATCTGCATTT	84708
rs766164672	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53621655	AATCAGACAATCAGA[C/G]AGAAATTTAAGGTAT	84708
rs766177448	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53505540	TACAGGAGTAAGCCA[C/T]CACGTCTGGCCCAAG	84708
rs766180256	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53629790	GGAGGCCAACACCCC[C/T]GACTTGGATAGAGCC	84708
rs766195521	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53516272	GAATCACGCAAAATG[C/T]CAAACAGTACCTGGA	84708
rs766198872	in-del	-/GT			intron-variant	LNX1	GRCh38.p7	4:53586954	TCACTTTACAGATGA[-/GT]GTATGTGCAGCTGAA	84708
rs766245676	snp	A/G	1.67736e-05	0.00289595	synonymous-codon	LNX1	GRCh38.p7	4:53496356	CAGGAGACGCACAGC[A/G]TAGTTGTGAGGGACA	84708
rs766309996	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53643220	CAATGGCACGATCAT[A/G]GCTCACTGCAGCCTC	84708
rs766311239	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53641231	CACCTCCTTTACTCT[C/T]TAAGAAGGAGGGATT	84708
rs766323325	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53636598	ACAGTTATACAAAAT[A/G]ACCAGCACATAGAAG	84708
rs766334557	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53615505	AGGAAGAAGACTGAG[A/G]CTCTAGCCAATCGCC	84708
rs766335877	snp	A/C			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53520505	CACCGAGTTCATTTC[A/C]TCCATACTTTGGGGA	84708
rs766340547	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53556929	GTTTTCATTTGCCCA[C/T]TGACTGTAATTTACA	84708
rs766389186	snp	A/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53518923	AGGAATACAAATGGC[A/T]CAGGCTGGCAAGTGA	84708
rs766415195	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53650596	AGAAATAAATAGATA[C/T]GTAAATAGAGGAGGA	84708
rs766442166	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53543188	TTATCCGAAGGTCAG[C/T]TGCCCTCATGGCTGG	84708
rs766459074	snp	A/G			intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53462534	ACCGTACCTTAAAAT[A/G]TTAACTGCTTTTTAG	84708
rs766464713	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53590790	GCACACTGCAAAGTC[A/G]TATTTAAAAGAGTGT	84708
rs766466709	snp	C/G			nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53603983	TGAAAACCACCTACT[C/G]TTACATGGGCTATCA	84708
rs766501779	in-del	-/AAG			intron-variant	LNX1	GRCh38.p7	4:53472494	AAGTATAATAAAAAA[-/AAG]AAGAAGAAGAAAGAC	84708
rs766525992	snp	A/G/T	3.3257e-05	0.00407769	missense, synonymous-codon, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508068	CACGTAGGCAGGGTT[A/G/T]TCTAGGCCAGGCTCG	84708
rs766538360	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53470204	ATGCAAATCAATAAA[C/T]GTAATCCAGCATATA	84708
rs766547930	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53479496	GTCTCATGAACCAGT[A/G]TCCATGACCATTTCC	84708
rs766558453	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53646385	TCAGTCTCTATCCTC[G/T]AACTCTGCTTTATTC	84708
rs766558684	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53607973	AAATCAGCTCAAGAT[A/G]AATTAAGAACTTAAA	84708
rs766563817	snp	C/T			synonymous-codon, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508200	CTTCCTATCTTTGGT[C/T]AGGCCGTAGTGGGAG	84708
rs766584303	snp	A/C			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53509300	AAATTCTTATCAATT[A/C]ATTACTCAAAACCCT	84708
rs766589962	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53635097	AGTCTTCCAAAGTGC[G/T]GGAATAGCACGCATG	84708
rs766591502	in-del	-/A			intron-variant	LNX1	GRCh38.p7	4:53650669	CTATACTACCGCCCT[-/A]ACATATAGGGCCTCT	84708
rs766593687	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53529876	CAAACACAGTTCTCA[A/G]AAAGCTTCTCTATTC	84708
rs766609715	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53617540	ATCCATCCTTCTGCT[A/T]CATGACATGGATACT	84708
rs766616439	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53606847	ATAAACATAACTAAA[A/G]ACAAAAACCCACATG	84708
rs766632878	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53615778	AAAAAATTTTTAGTG[C/G]GCATATAGTAGGTGC	84708
rs766655852	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53578936	AAAAATATGATTAAT[A/G]TCTCCCTGGTGGTTC	84708
rs766675661	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519804	CCCAGTTTGCAAATG[C/T]GGGAACTTAATACAA	84708
rs766690663	snp	C/T			intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53559165	GTCTACAGGATGAGA[C/T]GAGTTGCAATGAACT	84708
rs766715335	snp	A/G			upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53592762	GAGGGTGGAGGAAGA[A/G]GGAAAAATGGGAGAG	84708
rs766728362	snp	A/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53599733	TGAAGGGCCAGGCAG[A/G]GGAGGCTCATGGGAA	84708
rs766757248	snp	C/T			intron-variant, synonymous-codon	LNX1, LOC101928879	GRCh38.p7	4:53575823	GGTGGCAGCAATGGA[C/T]CAGCTACTAGGGGAC	84708
rs766762059	snp	C/T	4.94173e-05	0.00497053	missense	LNX1	GRCh38.p7	4:53496117	TCAAGCTGACCATGT[C/T]GATATGCCACACCGC	84708
rs766812238	snp	G/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53511461	TCAGATGGTGATGGG[G/T]GATGGCCATGAACTT	84708
rs766814203	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53629301	TGCATCCAGGAACTG[A/G]AAACTGTCCCCAGCA	84708
rs766823194	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53645238	GGCAAGGGAACTCTC[A/G]GGAGGCTGGAGCCAT	84708
rs766837779	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53513080	CTCCATCCTCTACCC[C/T]ACTGCATCTTAACCA	84708
rs766839233	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53587494	AGAGTCTATGTAATG[C/T]CAGTACATAAATATT	84708
rs766841007	in-del	-/CCT	3.32237e-05	0.00407563	cds-indel	LNX1, FIP1L1	GRCh38.p7	4:53461519	TTGTATTCTTCATAA[-/CCT]CCTACAATGCAGAAG	84708
rs766869717	snp	A/C/G	4.94265e-05	0.00497104	missense	LNX1	GRCh38.p7	4:53476798	GGGGACCAGTCACTG[A/C/G]GTGGGGCCATGTTGT	84708
rs766872249	snp	A/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53513061	CTCTGCCCCTGGTCT[A/T]GCCCTCCATCCTCTA	84708
rs766883204	snp	A/C	0.000171585	0.00926085	missense, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573723	TGAGGAGTTTGTTGA[A/C]CAGGATGCTGGACTT	84708
rs766918914	in-del	-/CT			intron-variant	LNX1	GRCh38.p7	4:53540714	AACAAAAAAACCCCC[-/CT]GTTATTATTATAAAC	84708
rs766927614	snp	A/G	1.64855e-05	0.00287097	missense	LNX1	GRCh38.p7	4:53476757	TTTGGACTTACCGTG[A/G]TAATTCCAGCCACAT	84708
rs766934286	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53553295	GTGCCCATACGGATC[C/G]CCTGGGGAGTTTGTC	84708
rs766936610	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53540982	TCTCTTCTAAAAATA[C/G]AAAAATTAGTTGGGT	84708
rs766974602	snp	A/G	3.29875e-05	0.00406112	synonymous-codon, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498683	CCGGCCGTCTCTGGC[A/G]ATCACCCCATCACGA	84708
rs766979577	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53486692	ATCTAATATTCAGAG[A/G]AAAAAAAGAGGGTTA	84708
rs766999871	snp	C/T	5.74564e-05	0.00535956	missense, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573642	TTTGAAAGTGATGCT[C/T]GAGGTCACAGCGCTG	84708
rs767003095	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53553540	GCAGGGCTGTAAATA[C/T]AGGGCCAGAAAGATG	84708
rs767004930	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53640936	GTCGGCAGTCCTTCC[A/G]GGGCCTTCCTCAATC	84708
rs767010011	in-del	-/TTC/TTCT	3.30127e-05	0.00406269	frameshift-variant, cds-indel, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460947	CAATAGTTAGAGTAA[-/TTC/TTCT]TTCTTCCTTTAAGTT	84708
rs767036842	snp	C/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53601221	TGTTATTAACTAGAC[C/T]GGGGATCCCTAAGTT	84708
rs767063909	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53530602	TCAAGTATTTTTAAA[A/T]TCTCTTACTTTGAAT	84708
rs767078746	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53588585	AGGCACTACCCAGTC[C/T]CCCCAGTCAGTCTGA	84708
rs767080861	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53552199	CTTGTCGTCCTCCAG[C/T]GACCCCGCCTAGCTG	84708
rs767127099	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53513178	CCTGATCCATATTAT[C/T]GATCACGGTCTCTTG	84708
rs767127649	in-del	-/T			intron-variant	LNX1	GRCh38.p7	4:53612706	AGCTAATTTTTGTAT[-/T]TTTTTTTTTTTGTAG	84708
rs767147305	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53514309	CTTTTGCTAATGAAA[A/G]AGCATGGGGTTGTAT	84708
rs767147567	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53501559	AAGTGCTAGGATTAC[C/T]GGTGTAAGCCACCAT	84708
rs767211298	snp	A/C			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53517899	TAGATCCGAGTATGA[A/C]CTTGAGGCTGAATGG	84708
rs767219285	snp	A/G	1.64784e-05	0.00287035	stop-gained, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498784	CACTGGGATCTACTC[A/G]ATTGATCTTGATGCT	84708
rs767220192	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53623888	TAAACCCAGGTCTGT[A/C]TGCACCTGAGCTCAA	84708
rs767252567	in-del	-/TAGT	0.000198046	0.00994906	frameshift-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460935	CAGGCCAAGAAACAA[-/TAGT]TAGTTAGAGTAATTC	84708
rs767263916	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53564216	TGTGTGGGGGTCACA[C/T]GGGCTGCATGGGCTA	84708
rs767277296	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53649701	CTCTGCCCATTTAGG[A/T]TTCCCCTTGGGCATC	84708
rs767280967	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53534564	GGAGGATCACTTAAA[C/T]CCAGGAGTTTGGGGT	84708
rs767282218	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53571480	GGAAGATGCTATGCG[G/T]CTGGCTCTGAAGATG	84708
rs767298001	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53627543	ACAAGATTTTCTGCT[A/C]TGAATTGATGCCCCC	84708
rs767299972	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53649724	TGGGCATCTCCTCTG[C/T]GCCCACCCAGTCTGG	84708
rs767326041	snp	G/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53506733	TGGTTGTGGGTGCCT[G/T]TAATCCCACCTACTT	84708
rs767332688	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53540911	GGAGGCTGAGACGGG[A/C]GGATCACTTGAGGTC	84708
rs767342252	snp	G/T	1.67632e-05	0.00289505	missense	LNX1	GRCh38.p7	4:53481732	CACCTTGGGAGTGTT[G/T]CTCCTCTCCCCTGGC	84708
rs767351567	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53607649	CAGGGAACTAAAAAA[G/T]AGCCCAAATAGCCAA	84708
rs767356741	snp	A/G			upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53592484	CATCATCCCATTGAA[A/G]CGCTGCGTATTTTTA	84708
rs767368929	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53637870	ACCACCACTCAAAGT[C/T]GCACCTTCTAACTTC	84708
rs767380947	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53523498	TGCCATGTTGGCTAG[A/G]CTGGTCTTGAACTCC	84708
rs767418781	snp	A/G	1.64784e-05	0.00287035	intron-variant, missense	LNX1	GRCh38.p7	4:53557913	TTGCCCACATTGTCA[A/G]TGTAGTTAGCAGGAC	84708
rs767424399	in-del	-/CCGTGTGT			intron-variant	LNX1	GRCh38.p7	4:53625843	CCCAGCAATTCCACC[-/CCGTGTGT]GTGTGTGTGTGTGTG	84708
rs767436287	in-del	-/CT			intron-variant, downstream-variant-500B, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460106	GCATGTGTACACACA[-/CT]CTTCATTGTGGCACA	84708
rs767479556	snp	A/C			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53510450	AGATGAGAAAACAGG[A/C]CTCCAACTTACACTG	84708
rs767486713	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53542865	CCCATCAGGAATAAA[A/T]CAGGGGGAAAGCAAG	84708
rs767499140	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53477644	ATTTTCCACCCAGAT[A/G]TTTTGCAGAAAAGAG	84708
rs767522467	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53527450	CCCACACCCATAATT[A/G]GTCTCTACGAGCCTG	84708
rs767525508	snp	A/G	3.57379e-05	0.00422702	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461404	GAAACAACATTTAAT[A/G]CAAGTATTTTTGATT	84708
rs767544337	snp	C/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53594096	GGATGTCTCCATTTG[C/G]AAATTAATTAGTAAT	84708
rs767584386	snp	C/T	3.34169e-05	0.00408746	intron-variant	LNX1	GRCh38.p7	4:53478551	AGTGCCTTTAAAATC[C/T]CTTTACTTTTTACCT	84708
rs767589932	in-del	-/T			intron-variant	LNX1	GRCh38.p7	4:53464929	TGAATTTCTTCTGTG[-/T]TTTTTTCTGAAAATC	84708
rs767602850	snp	A/G	1.64732e-05	0.0028699	synonymous-codon	LNX1	GRCh38.p7	4:53478644	CAAATCCCATTCTCT[A/G]TGTGATGCTCCCCCT	84708
rs767608543	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53521238	GCTCTTTTTGAGTCC[C/T]CGTGTTTTTGTGAAG	84708
rs767620997	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53572936	CTTCTTGAAGGACAG[C/T]TGTGCCTTGTCAATT	84708
rs767634524	snp	A/C/T	0.000206025	0.0101478	intron-variant	LNX1	GRCh38.p7	4:53496426	CAATCGTGCGGTCAG[A/C/T]TCCACCTGCCACAAC	84708
rs767635134	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53489179	AGCTCCTTCAATGAG[A/C]TAAAAGCAATCAGTC	84708
rs767640040	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53651307	CCCCCATCCTGCTCT[A/G]CACTGCGTCAGCATT	84708
rs767661895	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53463848	TTATATTTCCCCTTA[C/T]ATTACTAATTTAGTC	84708
rs767684214	snp	A/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53597230	AATTGATATTCCTGA[A/T]CAGTCCCTCTTCCTG	84708
rs767698047	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53524691	GCTTCTGAAGAGACT[A/G]CAAGTAAGGTTTAGG	84708
rs767698905	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53578558	ATTGACCAACATGTC[A/G]TTATGGGGTCCATGA	84708
rs767702757	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53547030	GAGGAAGAGACTGTA[C/T]GGTTACAGCAACTCC	84708
rs767709398	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53488287	TCCTATTGCCTGCCT[A/G]TTGGTCTAGTTATGC	84708
rs767718343	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53482750	CTGCCTATTTGGTAC[A/G]GTGTACACTATTCAG	84708
rs767734073	in-del	-/GTT	1.68091e-05	0.00289901	cds-indel, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461580	TACAATATCTTTACA[-/GTT]GTTATACAAGCACCT	84708
rs767747662	in-del	-/T			intron-variant	LNX1	GRCh38.p7	4:53482655	GTGGGAGCTTAGCTC[-/T]GGAGATGCAGAGGCA	84708
rs767749697	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53492343	CTTGAAGAGCACCAA[G/T]AAGGCAATGGGGCAC	84708
rs767751937	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53465379	ATAAACTAGTAAACT[A/G]GTATCTAATGCACTA	84708
rs767753949	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53545001	CATTGCACGAAGGTG[A/G]AGGGAGTGGTACCCA	84708
rs767759394	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53625349	TATGTTCACAATATA[C/T]ACAGAACTCTTGTAA	84708
rs767777650	snp	C/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53596337	CTTCTCTGGTTTGTG[C/T]GCTTTTGGGGAGAGA	84708
rs767799066	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53531692	TGAACAGGATTAAAC[A/G]TGAGACTGAAATGCC	84708
rs767813065	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53646532	GTGCCTGGCACAGAA[C/T]TGTCACCCAATCTAC	84708
rs767818335	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53509404	AAATCAAAGGTCAGT[C/T]TACCGTGATATGCAC	84708
rs767821964	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53548496	GTCTGTGATCAAGAA[G/T]TTGCAAGATTATTGC	84708
rs767863621	snp	C/T	1.65149e-05	0.00287353	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507449	ATCTGCTTCTAATAG[C/T]GGATCTCTCAAAGGG	84708
rs767887289	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53520859	CCCAGCTACTTGGGA[A/G]GCTGAGGCAGGAGAA	84708
rs767900205	in-del	-/TT			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53512827	GAGTGATTCTGAAAC[-/TT]TGCTTGAGGTGGGGT	84708
rs767930509	snp	A/C			intron-variant	LNX1, LOC101928879	GRCh38.p7	4:53575555	CACAAGTAGGAGCCC[A/C]GTGCAAACTAGGGCT	84708
rs767995478	snp	C/T			intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53575282	CCCCCATGCCCAGCC[C/T]AGATATTTCTTTTAA	84708
rs768004909	snp	A/T			intron-variant, downstream-variant-500B	LNX1, LOC101928879	GRCh38.p7	4:53577873	CAAGTGAGGTTTTTA[A/T]GTTTTGTTTTGTTTT	84708
rs768018905	snp	G/T	1.64773e-05	0.00287026	missense	LNX1	GRCh38.p7	4:53496092	GATGGCTAACACACG[G/T]TCATTCTCCTCAAGC	84708
rs768027645	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53491313	AATGCAGTTTCTTCA[C/T]AAAGAAATACAATGG	84708
rs768033811	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53542371	GATTGAGCTGAATGC[A/G]CAGTGTCTTGGGATT	84708
rs768052554	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53631878	TTTTTTTTTTAAGTC[C/G]TTGAGAATCCTTGAC	84708
rs768060216	in-del	-/TGA			intron-variant, downstream-variant-500B, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53459944	GATATCACAACTTTT[-/TGA]TGATGGCTTTTCAAT	84708
rs768068783	in-del	-/CA	1.87845e-05	0.00306462	utr-variant-5-prime, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53574038	AACAGGAAACTCAGT[-/CA]CACAATATTTCCTCA	84708
rs768094254	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53502480	AAACATGCTGTTTAA[C/T]GATCATCTGAGGCTT	84708
rs768101882	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53642898	TATGGTCGCCTGGGT[A/G]TAACTTTAGTCTCCT	84708
rs768102232	in-del	-/CTAA			intron-variant	LNX1	GRCh38.p7	4:53616004	TCTTACTAATTCTTT[-/CTAA]CTAACTATTTTTTGT	84708
rs768102630	snp	C/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53510149	AGAACATTCAAAAAG[C/G]ATTGCCTATTTCATG	84708
rs768111489	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53489389	TTAATGATAATACAG[A/G]TGGTGACTTATATGG	84708
rs768113442	snp	C/T	3.30934e-05	0.00406763	intron-variant	LNX1	GRCh38.p7	4:53476705	GTGGTTTAAGAAATG[C/T]AATCGTTTTCTCCCA	84708
rs768123234	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53618963	TGCTATGTTACGCAG[G/T]GTGGTCTCTAACTCC	84708
rs768158951	snp	A/G	3.295e-05	0.00405881	missense	LNX1	GRCh38.p7	4:53496249	AAGCTGTCATCTCGG[A/G]GTCTGTAGGCATCCG	84708
rs768174861	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53570988	GCAGAGATCGCGCCA[C/T]TGCACTCCAACCTGG	84708
rs768178284	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53619685	TATTCATGTGAAAGT[G/T]TTCACAAGAACCAAT	84708
rs768184541	in-del	-/T	1.70075e-05	0.00291607	frameshift-variant, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507989	CATTTGACTCACCCC[-/T]AGTTCGGTTGCTCCG	84708
rs768187046	snp	G/T	1.6525e-05	0.00287441	utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460903	CTCTGACCCATCATT[G/T]ATTCTATAAAAAAGT	84708
rs768209163	in-del	-/T	6.82576e-05	0.00584159	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498592	GTTTGCTCAGAAGCA[-/T]TTTTTTATATCAAGC	84708
rs768213120	snp	C/T	1.68587e-05	0.00290329	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508037	TGATTGCTGGCTGCC[C/T]GTCCTCTGCCGAGGA	84708
rs768220506	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53475597	TTCATTTTTCCATAT[G/T]TAGTCCTATGCTAGT	84708
rs768227161	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53556359	GCTGACACCTTGATT[C/T]CAAGCTTCTGGATGC	84708
rs768238562	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53615152	CAGTAGAAAACAGGC[C/T]GTGGGAGATTTAGTG	84708
rs768263433	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53651602	TTAAAGAGTAGGGTC[A/T]CCATTCTACTGAAAA	84708
rs768268551	snp	A/C	1.6473e-05	0.00286988	missense	LNX1	GRCh38.p7	4:53496181	CATCCACCTTGCGCA[A/C]CAGTTTTATTCCAAG	84708
rs768272972	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53549161	ATGTACCCCCCAAAT[C/G]TAAAATAAAAGTAAA	84708
rs768294452	in-del	-/AAC			intron-variant	LNX1	GRCh38.p7	4:53583932	AACTGACCCCCTGCA[-/AAC]AACAACAACAACAAC	84708
rs768302067	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53584671	CCATATGACGACCTC[C/T]ATGTGAGGTTTTAAA	84708
rs768302211	in-del	-/GGATC			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53602123	GAGAAATAGAAACTA[-/GGATC]TGTCTGTGCAGAAAC	84708
rs768305235	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53585689	ATTGGAATTATGCAC[C/T]CACAAGCTAAGGAAT	84708
rs768309606	snp	C/T			intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498400	ACAGACAAAATGATA[C/T]AGAGACAGATAAATA	84708
rs768317193	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53557359	GGCATGTTTCTTCGT[A/T]TCCCATAGGTTTCAA	84708
rs768342257	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53465875	ACCTTGGCAATGTGT[A/G]TACACATTTTTAATC	84708
rs768344704	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53497051	GCAAAAGGAAGAAAT[C/T]CTTGCACAGTTTCAG	84708
rs768360402	in-del	-/A			intron-variant	LNX1	GRCh38.p7	4:53530985	CCTGGCCAACATGGT[-/A]AAAACCCCGACTCCA	84708
rs768370061	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53486199	TTTCCGCCCTGCGCC[A/C]GTTCACCCCTCCTTA	84708
rs768408647	snp	C/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53596975	TACATTCTTTCTGGA[C/T]GGACTGTACTGTCTG	84708
rs768423371	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53626981	TTGACAAAATGTATT[A/C]TAAAGATTGGCCGGG	84708
rs768454987	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53646887	TTGTTCCAATTTAAC[A/G]TGAGTAAATAAACCA	84708
rs768508591	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53482381	AATATGGGGATGACT[G/T]CATACATTAATATGT	84708
rs768525512	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53492864	CCTTTGCCTTATCCA[A/C]AGGAAGATATGAAGC	84708
rs768529230	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53637579	CCCACGACACTGTAA[A/G]GTAGGCTTGTTTCAT	84708
rs768544463	snp	C/T	1.85661e-05	0.00304676	missense, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573803	TTCTCCACCAGGAAG[C/T]TGGTGAGGCAGAGGG	84708
rs768557996	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53509170	ACTATCTCACTCTAC[C/T]GTGGGGAGGGTAGCT	84708
rs768566872	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53563438	TAAGTATTCTTCTTA[A/G]TATCCCTCCTAAGGG	84708
rs768588372	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53638360	GTCAACCCTTATTAT[C/T]TGCAGATTCCATAGT	84708
rs768621160	snp	C/T	1.6477e-05	0.00287024	missense, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498765	AGCCTAATAGAGAGG[C/T]TTTCACTGGGATCTA	84708
rs768624493	in-del	-/A			intron-variant	LNX1	GRCh38.p7	4:53584775	TTTCAAGATCCCTAC[-/A]GCACCTACCAGCTTC	84708
rs768634190	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53608545	CAGCCACCGTGGAAA[A/G]CAGTGTGGAGATTTC	84708
rs768652360	snp	G/T			intron-variant, downstream-variant-500B	LNX1, LOC101928879	GRCh38.p7	4:53577953	GAATATTTACCATGC[G/T]CCAGGCACTGTGCTA	84708
rs768670446	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53579808	GATGTAGTTGCCAGA[A/G]TAAACCACATACTCC	84708
rs768676304	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53615429	CCTTGCCCTCTTGGA[A/G]GCTTGAAACTGCCAT	84708
rs768681066	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53627953	TCATTCTGACTTCAC[A/G]AGTCTCTGAGGAAAA	84708
rs768718349	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53552932	ATTCAAGTACAGTGC[C/T]GCATCCTGAAACATC	84708
rs768720741	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53524277	GAGCTAGTGATGAAG[A/G]ATGGAGGTTTCCTGT	84708
rs768729947	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53500562	GAATTAATAAGTACT[C/T]AACTCTCTAAGAACA	84708
rs768748977	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53587983	TTTTTTGCTCAGTCT[C/T]TGGCCCTCAACGTAC	84708
rs768754306	snp	C/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53520429	GTCCACATGCCAGGT[C/G]AATTCTTCAGAGACG	84708
rs768837817	snp	C/T	8.30792e-05	0.00644459	missense, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461507	GGTTTGTTTCCATTG[C/T]ATTCTTCATAACCTC	84708
rs768849985	snp	C/T			upstream-variant-2KB	LNX1	GRCh38.p7	4:53654474	CTCCTTTCTCATCTG[C/T]GAGCAACCGGATTAG	84708
rs768858390	snp	C/T	1.7134e-05	0.00292689	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461607	ACCTGAAATAGAATG[C/T]AATCAGTGTACATGC	84708
rs768878942	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53541967	CATAAATCAGCTGCT[C/T]CAGATGACACATGGC	84708
rs768885349	snp	G/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53600865	CCTCCTGAGTAGCTG[G/T]GATTACAGGTGCCCA	84708
rs768895515	snp	C/T	1.68224e-05	0.00290016	intron-variant	LNX1	GRCh38.p7	4:53496422	GGAACAATCGTGCGG[C/T]CAGCTCCACCTGCCA	84708
rs768916984	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53534980	TACAAAGAAACCAGT[A/G]GTGTTAACCTGTTGA	84708
rs768936037	snp	A/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53598319	TTTACTGTAGCCTTG[A/G]CCTCCTTATGATTAA	84708
rs768936087	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53611788	AAGTAAACCAAAGCT[C/T]TTACCAAGAAATCTA	84708
rs768939340	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53475665	CATTGGAACAGCAAG[A/G]TAATCATCTGAAGGC	84708
rs768944364	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53484779	GTAAGAGTGTCTATT[A/G]TAACATCAAAATGGA	84708
rs768948566	snp	A/G	6.69961e-05	0.00578736	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498624	CCTTGCTGCAGCCCC[A/G]CAGCCACAGTCTCTA	84708
rs768951303	snp	A/G	0.000155703	0.00882196	intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573581	GGGTCCAGCTGTCCC[A/G]CTTGGGGGTGGGACT	84708
rs768959787	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53619823	GCACCGTTTTACACA[C/T]CCAGCAGCAATGCAT	84708
rs768964148	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53648983	AGAGGAGGTCTCCTT[A/G]GCATGCAGGGCAATG	84708
rs768997797	snp	A/G	1.64746e-05	0.00287002	missense	LNX1	GRCh38.p7	4:53478624	ACACTGATGACATAG[A/G]TAGGCAAATCCCATT	84708
rs769015357	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53611061	AAAAGAGGTAAAACT[A/G]TCTATTTTTGCAAAT	84708
rs769018059	snp	A/C	1.6483e-05	0.00287076	missense	LNX1	GRCh38.p7	4:53478705	TCTTTTTGGATATTT[A/C]CCACCTTCTCATGAC	84708
rs769020459	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53522792	ACAGAGCAGGGCCCT[A/G]TCTCAAAAACACAAA	84708
rs769043391	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53506229	TCCCTCTGGGTCTCC[A/G]TTTTCTCATCTGTAA	84708
rs769060518	snp	C/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53599330	TGAGTAACCTCTGGT[C/T]GTCCTCACTGCTACA	84708
rs769098124	in-del	-/CAGCATAGTTTCCA			intron-variant	LNX1	GRCh38.p7	4:53497676	TGCAACCCTGCCAGG[-/CAGCATAGTTTCCA]CTAGAACTGGGAGGC	84708
rs769113166	in-del	-/A			intron-variant	LNX1	GRCh38.p7	4:53606488	AACAAAAAACAAACA[-/A]AAAAAAAACAGAACA	84708
rs769125617	snp	C/T			intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53558429	TCCAGTTTGCTATAG[C/T]GACACTGTAAGAAAT	84708
rs769145351	snp	A/G			nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53604684	TGCAACCAAAAATGA[A/G]TTATGAATATCAGTC	84708
rs769152081	snp	A/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53593620	GGTGAGATCTTTCTT[A/G]GTACTCCTGGATTTC	84708
rs769155171	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519967	GCTGGTGCTCACCCT[A/G]TAAGTGACAGAGACA	84708
rs769169110	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53611172	TGGATCTACAAACAG[A/G]CAAAAATACCATTAG	84708
rs769181910	snp	C/G			intron-variant, utr-variant-3-prime, downstream-variant-500B	LNX1, FIP1L1	GRCh38.p7	4:53459888	TTTATCATTACTGCT[C/G]TGACACTCTTGCTTA	84708
rs769195264	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53506355	AGCTGTTACTACTAC[C/T]CTAAAGTTCTAACAT	84708
rs769216745	snp	C/T			upstream-variant-2KB, nc-transcript-variant, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53593032	AACAACAACAACCAC[C/T]ACAACAAAACTATTC	84708
rs769238111	in-del	-/GAGA			intron-variant, utr-variant-3-prime, downstream-variant-500B	LNX1, FIP1L1	GRCh38.p7	4:53459856	GCCCCTCTAAGGCTT[-/GAGA]GAGATTAAAACTAGT	84708
rs769243440	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53622388	TAATGTCCCGGTGTC[G/T]CAGGAGTGAACAGTA	84708
rs769257271	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53633391	TTTATATCTTCCTCA[C/T]ATTATTGCTTCTTCC	84708
rs769283764	snp	G/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53517175	TAAAAGCAGCTAATT[G/T]TTTTCTTGCTCCTTT	84708
rs769286338	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53570770	TGGTGGCTCACGCCT[A/G]TAATCCCAGCACTTT	84708
rs769306139	snp	A/C	1.69755e-05	0.00291332	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507508	CAGTAGTTATGATTT[A/C]ATAGAAATAATCATT	84708
rs769307260	snp	A/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53594583	TCATTGCTAAAGACC[A/G]TGACACTTTTCAACT	84708
rs769311467	snp	G/T			upstream-variant-2KB	LNX1	GRCh38.p7	4:53653939	CTCCAGTGGGCCCAA[G/T]TTGTCTGTTCTCATA	84708
rs769332027	in-del	-/A			intron-variant	LNX1	GRCh38.p7	4:53625459	GTCAATAAGCACATG[-/A]AAAAGATGTTCAACA	84708
rs769336727	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53545430	ATGACAACACAGTAG[C/G]GATGCAGTCCTGGAA	84708
rs769339958	snp	A/G			intron-variant, utr-variant-3-prime	LNX1, LOC101928879	GRCh38.p7	4:53576469	GCTGACTCTTCCCAG[A/G]ACAGCCCTGCCCTTC	84708
rs769343907	snp	A/G	1.89712e-05	0.00307981	utr-variant-5-prime, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53574044	AAACTCAGTCACACA[A/G]TATTTCCTCAGGAGC	84708
rs769353726	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53539674	ATGTTTTTGTTCTAA[C/G]TTGTTTAATGCCTGC	84708
rs769360834	snp	A/C	8.40696e-05	0.00648288	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508024	GAGTCCACTGGGCTG[A/C]TTGCTGGCTGCCCGT	84708
rs769457082	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53546999	TCAGCCATTTCCCTG[C/T]CTCTTCAGTGAGAGG	84708
rs769462121	snp	A/G			intron-variant, splice-donor-variant	LNX1, LOC101928879	GRCh38.p7	4:53575402	TAGGAAGTCTCTTGC[A/G]TAGAAAGTCAATAAA	84708
rs769467329	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53484301	AGGACCTTGTTTTAA[A/G]AATCTCAAGTAAACA	84708
rs769468228	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53644006	CAAAATTATTTACTC[G/T]AAAAGTCTTATTAAT	84708
rs769473912	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53529360	CAAGGTACTTCTAAT[G/T]TTCCCTAGTCCAGAG	84708
rs769476127	snp	A/G	1.65108e-05	0.00287317	stop-gained	LNX1	GRCh38.p7	4:53496061	CTGGGCTGCCATATC[A/G]AAGATCATGTCCATT	84708
rs769478103	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53516211	TGGGCTACTGCACTC[C/T]AGCCTGGGCAACAGA	84708
rs769500190	snp	A/G			nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53603746	AATCATTCATGAGAA[A/G]TCTGCCCCCATGATC	84708
rs769502400	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53616698	TAGCAGCAGCTAATA[A/T]TTATTGAAACCTTAT	84708
rs769520904	snp	C/T	8.23649e-05	0.00641683	missense	LNX1	GRCh38.p7	4:53496177	GGCTCATCCACCTTG[C/T]GCACCAGTTTTATTC	84708
rs769548916	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53586815	TCTTTTTAGAATATA[A/T]AATAAAAAATAATGA	84708
rs769572352	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53503220	TGTTGATATTTTGAC[C/T]TCCTCCCATGAATCA	84708
rs769573807	snp	A/G/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53522385	CTAAAGTCTACTAAA[A/G/T]GTAAGGCACCAGGCT	84708
rs769598947	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53490247	GTCTGGAATTGCCTA[C/T]GGAAAAAAGGCTTAA	84708
rs769611922	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53469032	CCTAAATCAACAGAA[A/T]ATACATTCTTTCCAG	84708
rs769648221	in-del	-/ATTG	1.65295e-05	0.0028748	utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460899	TTCCTCTGACCCATC[-/ATTG]ATTGATTCTATAAAA	84708
rs769650888	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53483676	AAGAGAGAGGAGTAA[C/G]GTTTGGTGGTTCCTC	84708
rs769654689	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53627827	TGAGTTAGAGCAGAA[A/G]CCCTCCTCATTAGCC	84708
rs769658972	snp	C/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53597187	TTGCAATGCTAGCTG[C/T]ACTTGTCACTCTCCT	84708
rs769661220	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53465124	TGAAAAACATCTTGC[A/G]TTTTTTTCCTTGCAG	84708
rs769673716	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53550770	TCATGGCCCAATACC[A/T]GGCCCAGGTCTGACT	84708
rs769685162	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53526705	CAACCCAGCTTAAAG[G/T]CATCTTTTAAGAGCC	84708
rs769735365	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53548431	TATATAATTTTATAT[A/C]GATAACTATACATAA	84708
rs769751252	snp	A/C/G	0.000453375	0.01505	intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573606	GGGACTTACCGGCTC[A/C/G]CTGATGGGGGACCTA	84708
rs769777564	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53615336	GTATTTCTTACTCCC[A/G]TGAATCTACCTGGGC	84708
rs769785479	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53585910	CATATTTCCAGGGGT[A/G]TTCCTGCAGGAATGG	84708
rs769814233	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53634732	CTCTGATCACAGGGA[C/G]TGCTCCGAGGGGTGG	84708
rs769817327	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53534454	GCAGCCTGGGCAACA[G/T]AGCAAGACCTTGTCT	84708
rs769820442	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53562126	ATGCAGATGATGAGA[C/T]TACAAAATGGAAATG	84708
rs769822088	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53572786	TCTGCCACCAGTGTG[G/T]GTGTGTGTGTGTGTG	84708
rs769843757	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53542853	GAACCCCCCTCTCCC[A/G]TCAGGAATAAATCAG	84708
rs769850047	snp	C/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53600344	ATGGAGTGGGAAAGG[C/T]AAAAGCCAGAGGAGA	84708
rs769866573	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53636675	ACTTTGATAGTAATT[G/T]GGCAATAGGACAGCA	84708
rs769870446	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53513586	ACTAAATAGCTCCTT[A/G]TCTGTCATTCAGGCC	84708
rs769875609	snp	C/T	4.86748e-05	0.00493306	synonymous-codon, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573679	CTGGGTGCAGTGCTC[C/T]CTGAATGGGCAGGTC	84708
rs769881410	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53619425	GCCTATTTTGGACAT[A/T]TCATATAAATGGAAT	84708
rs769912039	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53509863	GCAAACCCAGTCGCA[C/T]GAGTACCCCTTATCA	84708
rs769969759	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53589910	TGCTGACATACAGTG[A/G]TGAAATTATTTATTT	84708
rs769982111	snp	A/G	1.66449e-05	0.00288482	synonymous-codon	LNX1	GRCh38.p7	4:53481795	GGCTTCCTGAAAGAT[A/G]TCAGGGCTCCGCTGC	84708
rs770000194	snp	A/G	1.79544e-05	0.00299615	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461387	CAAGCTTTGGCATTT[A/G]TGAAACAACATTTAA	84708
rs770023997	snp	A/G	1.64939e-05	0.0028717	intron-variant	LNX1	GRCh38.p7	4:53557825	TCGGGTCCCACCCCC[A/G]ACATACTAGGCACAT	84708
rs770037317	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53651579	AAGAATGTACTCTGG[A/T]ATTTTGTTTAAAGAG	84708
rs770055718	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53640675	ATTGTTGTCAACAGT[A/G]GGAACAATTAAGACT	84708
rs770065637	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53525870	GCTAGGCTGGGCTGG[C/T]TAAGATAATGAAATT	84708
rs770070633	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53554239	ACTGGACTCTCTCCC[C/T]TATATGTAAGTCCCC	84708
rs770089999	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53564852	GCAAGGAGTCAGGGA[C/G]TTAGTTCCCTTTCCT	84708
rs770112996	snp	A/G	8.38633e-05	0.00647492	intron-variant	LNX1	GRCh38.p7	4:53496420	GTGGAACAATCGTGC[A/G]GTCAGCTCCACCTGC	84708
rs770130234	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53641813	TGGCTTACTTCACTT[A/G]GTATGATAATTTCAG	84708
rs770151628	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53495273	TCTTAAAATAAAAAA[A/G]CTAAAGAAAAAAAAA	84708
rs770153968	in-del	-/TT			intron-variant	LNX1	GRCh38.p7	4:53612697	TGGTATGCCAGCTAA[-/TT]TTTTTGTATTTTTTT	84708
rs770162008	snp	C/T	4.94246e-05	0.0049709	missense	LNX1	GRCh38.p7	4:53478621	TCAACACTGATGACA[C/T]AGATAGGCAAATCCC	84708
rs770173015	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53474301	TACATATAAACACAG[A/G]CCAGGGGTGAGCAAT	84708
rs770203909	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53589083	AGGAGACCAAACACC[A/C]AGTCTGCCCTGGAGA	84708
rs770209219	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53512798	TAGGTATTAGCTGCT[C/T]TACTGAATGGGATGA	84708
rs770209343	snp	A/T	8.30006e-05	0.00644154	intron-variant	LNX1	GRCh38.p7	4:53477027	AGTGAGAGCACAAAC[A/T]GGGACTTCTGCTTAA	84708
rs770217051	snp	A/G/T	5.19066e-05	0.00509422	missense, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573969	ACACTGCACACAGGG[A/G/T]TTCAGGATCGTTGGC	84708
rs770234229	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53650217	ACACAAATGCATAGC[A/G]CGTGTCACAGTCCTT	84708
rs770243216	snp	A/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53517358	GAAATCTTTATTGTG[A/T]GAGATAAAAATAAAT	84708
rs770275275	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53536466	ACCAGCAACTCCTGA[C/T]CTAAAAAAGTTTCCT	84708
rs770335800	snp	A/G	1.74078e-05	0.00295019	synonymous-codon, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573849	CACACGGAGTGTCCA[A/G]GGGGTCCAGCAAAGC	84708
rs770335898	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53583248	AGACTCTCATGTAAT[A/G]GGGAAGAATTAGGAG	84708
rs770336988	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53624559	TCTTTATCAGCAGCA[C/T]GAAAATGGACTAATA	84708
rs770340746	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53486334	TCAAACGACTCTCCC[A/G]CCTCAGCATCCAGAG	84708
rs770345720	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53644924	GCACAGTCAAAATGC[A/G]CTTCTCAGTTTTCAA	84708
rs770357355	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53563778	GACCTCGTGATCCAC[A/C]CGCCTCGGCCTCCCA	84708
rs770366448	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53536594	GATCTCAGGGCCTCT[A/G]TGTCCCTGGTTTGGT	84708
rs770393681	in-del	-/TT			intron-variant	LNX1	GRCh38.p7	4:53607221	GAAAATTCCATAGTC[-/TT]TGCCTAAAAGCTCAC	84708
rs770399124	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53463171	AAACATAACCATCAA[A/G]AATATTACGTGTTCT	84708
rs770441924	snp	A/C			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53500640	GTGGGCAGAGGAAAC[A/C]CGAGATGTTGTAAAT	84708
rs770449117	in-del	-/A			intron-variant	LNX1	GRCh38.p7	4:53471455	CATGTCTAAAACATC[-/A]AAAAGCAATGGCAAC	84708
rs770471744	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53535406	AATGAAATCTCTCCC[A/G]TCCATCAAGAATAGC	84708
rs770490631	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53509092	TGCCATGAACATGAA[C/T]ACTGCCACTCGGCAA	84708
rs770531645	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53636178	TGCACATCTATTACT[C/T]CTTTTTTTTTTTTTT	84708
rs770537672	snp	C/T			intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53558597	CAGTGACAGCTTCCT[C/T]GCTAATTTTGAAATC	84708
rs770549464	snp	C/T	1.6557e-05	0.00287719	intron-variant	LNX1	GRCh38.p7	4:53477004	CCAGAGAAGCAGAAG[C/T]TATCTTTAGTGAGAG	84708
rs770575097	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519115	CATGCCCAGGCTGGC[C/T]GTCTCACTGCCCCTC	84708
rs770594887	snp	C/G	1.64811e-05	0.00287059	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507408	CCTTCGAAGAACACT[C/G]AAAGCTCGATTTATT	84708
rs770597167	snp	A/G			intron-variant, nc-transcript-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53500453	TAAGAGTCTCCTTTC[A/G]TTATGGCATCTGGAA	84708
rs770627472	snp	A/G			intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53559627	AACAAAGGGCTTAAC[A/G]AGTATTAGCTTAATG	84708
rs770631954	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53529415	AACTGGGTAACGTGG[A/G]TGCTGATTTTTAAGG	84708
rs770641210	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53606081	CAGTTAGCAGAAGAC[A/G]GGAAATAATCAAAAT	84708
rs770643239	snp	C/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53593833	GGTATCATTGCTATT[C/T]GCATTCTACAGCTGG	84708
rs770652814	snp	A/G			intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53462130	TAGAGAAGCATGCAC[A/G]CATAAAGTGAATGGA	84708
rs770660076	in-del	-/AAAAAAT			intron-variant	LNX1	GRCh38.p7	4:53625640	TGTCTCTACAAAATA[-/AAAAAAT]AAAAAATAAAAATAG	84708
rs770673548	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53547027	AGGGAGGAAGAGACT[A/G]TATGGTTACAGCAAC	84708
rs770705157	snp	A/T	7.1727e-05	0.00598818	intron-variant	LNX1	GRCh38.p7	4:53481882	ACACAGGCATTAGCC[A/T]CTGTCAGTTTCCATC	84708
rs770716676	snp	G/T			intron-variant, nc-transcript-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53522997	CTATCCAGTGGTTCT[G/T]AACCTTGGCTGAGCA	84708
rs770723608	snp	C/G/T	3.30591e-05	0.00406554	synonymous-codon	LNX1	GRCh38.p7	4:53496059	TTCTGGGCTGCCATA[C/G/T]CGAAGATCATGTCCA	84708
rs770724547	in-del	-/AAC	1.68845e-05	0.0029055	intron-variant, cds-indel	LNX1, FIP1L1	GRCh38.p7	4:53461059	TAAAAAAAAAAACAA[-/AAC]AAGATATGATTAGTA	84708
rs770743182	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53480386	ATTCTAAAACCACAG[C/T]GCAGATGGAGGCTAC	84708
rs770760614	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53627884	GAGATTTGAAGATGA[A/G]GGTTTCAATGGGATG	84708
rs770767618	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53644870	TAAGGGAGAGATGTG[G/T]TAACAGGGAGGAGGA	84708
rs770783622	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53618135	CATTTAAACAAATTG[C/G]CCTTAACTACTTTGC	84708
rs770790071	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53464579	TTATGAGAGAAATGC[C/T]GAGTCCCCATATTAA	84708
rs770793109	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53466740	GAGCCTTGCTCATTG[C/G]TAGCACAGCAGTAAA	84708
rs770800928	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53587001	TTGTCATTCATTTAT[C/T]AATTCATTCACTCAT	84708
rs770817070	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53489536	CTTTTAGGATATCTA[C/G]AAGTTACTCTCATGA	84708
rs770861327	snp	A/G	1.72362e-05	0.00293561	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461615	TAGAATGTAATCAGT[A/G]TACATGCATATTTAA	84708
rs770904883	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53490561	ATATGTAAAGCTGGT[C/T]AAATATAAAATGGTT	84708
rs770911002	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53546312	GTCGAGGAAATCCCA[C/T]GTTACCATTCTGAGC	84708
rs770920708	snp	C/T	1.65471e-05	0.00287633	intron-variant, missense	LNX1	GRCh38.p7	4:53557965	ACAGAAGCGCCTTCA[C/T]TCTCCGAGCAGTGTG	84708
rs770928458	snp	C/T	1.70133e-05	0.00291657	intron-variant	LNX1	GRCh38.p7	4:53481703	CAGGAGCAGGCGACC[C/T]GCCCTAGAGGCCTCA	84708
rs770950464	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53646907	TAAATAAACCACTCC[C/G]ACCCCTTTGCCCGGG	84708
rs771001062	in-del	-/C			intron-variant	LNX1	GRCh38.p7	4:53526973	AATAGAAATGAAACA[-/C]CTAAATGAAGGGTGA	84708
rs771016443	snp	A/T	4.95258e-05	0.00497599	missense, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460936	CAGGCCAAGAAACAA[A/T]AGTTAGAGTAATTCT	84708
rs771043922	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53540549	TAGCTGGGCATGGTG[A/G]TGGGTGCCTGTAATC	84708
rs771052911	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53619584	GTCCATTGTAAGGGT[A/G]TACAGCACATGTTGT	84708
rs771095621	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53637230	AAAGGACTGCCTTGG[C/T]CCCTAAGAAACTTGT	84708
rs771143665	snp	A/C	1.66302e-05	0.00288355	missense	LNX1	GRCh38.p7	4:53481789	CCAGCCGGCTTCCTG[A/C]AAGATGTCAGGGCTC	84708
rs771152814	in-del	-/CC			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53515508	CACTTCAATTTAAGG[-/CC]CCCACCCCACCAAAA	84708
rs771217727	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53470688	CAAGCATTCTTATAC[A/C]CCAATAACAGACAAA	84708
rs771226520	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53554281	GTGTCTCATTTGCCA[A/G]TTCTGGGTCTGCTCT	84708
rs771230901	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53555832	TATAGATTGCTTGTG[C/T]CCGTTCAGTTATTCA	84708
rs771233328	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53620822	AATCAGTGTTAGCTC[A/G]CAGTGCAGCACGCTC	84708
rs771249384	snp	A/C	1.67531e-05	0.00289418	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508261	GGAGGTGAAGAAGAG[A/C]TTTGGCTCTGCTGCC	84708
rs771267548	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53581629	ATGTGCAGGGGAACC[A/G]CCCTTTATAAAACCA	84708
rs771312072	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53543109	CAAACAATTCTCCTG[A/C]CTCAGCCTCCCGAAG	84708
rs771316428	snp	C/T			utr-variant-3-prime, downstream-variant-500B	LNX1, FIP1L1	GRCh38.p7	4:53460381	TGGTATTTGAAAGAA[C/T]AAATTACTAGGATCT	84708
rs771325613	snp	A/G	1.65083e-05	0.00287296	synonymous-codon, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508158	GAGGCTCGCACAGCC[A/G]TCTGGACAGCCATCT	84708
rs771333592	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53502258	CCCCTATGGCTGCTA[C/T]GGTCATTAATTTATA	84708
rs771346244	in-del	-/TT			intron-variant	LNX1	GRCh38.p7	4:53545807	CAGAGGCCACATTTT[-/TT]TTTTTTTTTTTTTTT	84708
rs771372029	in-del	-/G			intron-variant	LNX1	GRCh38.p7	4:53490972	GGCTTTGTTTAGTAA[-/G]CAAAAGAATCTTTTA	84708
rs771382995	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53641950	ATTTGGGTTGTTTCC[A/C]GTCTGAGGCTATTAC	84708
rs771411959	snp	A/C			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53514094	GCCTCTGATTAAAAT[A/C]CCTCTTCTCTGACCA	84708
rs771421531	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53584445	GGCAATGTGTATAAT[A/G]CCCCAAGACAGGAGC	84708
rs771430050	in-del	-/T	1.64898e-05	0.00287135	frameshift-variant, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507421	TCAAAGCTCGATTTA[-/T]TTTTTTTAAATGATC	84708
rs771437348	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53650899	CCAGGCACATGGTCA[C/T]CACAATAGTTAGTAT	84708
rs771438101	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53630569	TGCCGCCTGGTGTTC[C/T]TAAGTGCAAGAAGGC	84708
rs771443063	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53562054	AGGCAGAAATCACAA[C/G]TTATTTTTCTTTCAT	84708
rs771477712	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53613686	GCATATATATGCCAC[A/G]TTTTCTTTATCCAGT	84708
rs771488588	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53642105	TACACGCCTGTGATC[A/C]CAGCTACTTGGGAGG	84708
rs771497205	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53487254	CCATACAGTGACTAT[A/G]AGGGCCAGTGAAAAC	84708
rs771533789	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53572529	GATTCATGACCTAAG[G/T]TATGTGACCTTTAAA	84708
rs771535224	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53497908	AGAAGGGATGGGATA[A/G]AACTGTTATCTGAGT	84708
rs771537117	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53496978	CTGTGTGTGTGCGGA[C/T]GGGAATGTGTCAGGT	84708
rs771555872	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53464370	TTGTTTTCCTAGTTT[A/G]TTGTAGACTAATACT	84708
rs771579483	snp	A/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53605388	GTCAAGCAAATTAAC[A/G]TATGCATCATCTTAC	84708
rs771581987	in-del	-/AGTT	0.000139213	0.0083419	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461093	TTAATTCGTTGCTGA[-/AGTT]AGTTAATGCAAGTTT	84708
rs771601884	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53526144	TAACATACGCCACGT[C/T]CAGCAGGAAACCTCT	84708
rs771611506	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53500304	TGTTCAGAGGGGACA[C/T]CAACAAGTGATGGGA	84708
rs771624893	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53487532	CTCTCCCCACAATGC[C/T]CCAGGGTATTATTCT	84708
rs771634890	snp	C/G/T			intron-variant	LNX1	GRCh38.p7	4:53651517	AGGAGAGTTCCAATT[C/G/T]CTAAAATTCCATCCT	84708
rs771639221	snp	C/T			intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498199	TCAAAAAGTAGATGA[C/T]TGTGATTAAATAAAA	84708
rs771660302	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53625762	TAGTAAGCCACGACT[A/G]CATCACTGCACTCCA	84708
rs771691242	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53482195	AGTTCTTCCCAGATA[A/G]AATTAGGTGCACTGT	84708
rs771694877	snp	A/C	1.66385e-05	0.00288426	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507296	CCCATGTCCATCCAG[A/C]CTTATGGGGAGTTCA	84708
rs771731130	snp	A/G	3.60549e-05	0.00424572	synonymous-codon, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573820	GGTGAGGCAGAGGGT[A/G]CAGTAGGTGTGTCCA	84708
rs771769366	snp	C/G	1.65888e-05	0.00287996	missense	LNX1	GRCh38.p7	4:53496333	CACAGCACCTGGCAG[C/G]GCTGCCGCAGGAGAC	84708
rs771780717	snp	C/T	0.000100169	0.00707632	missense	LNX1	GRCh38.p7	4:53481805	AAGATGTCAGGGCTC[C/T]GCTGCCGAACCTGGC	84708
rs771784538	snp	A/C	3.41822e-05	0.004134	stop-gained, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573930	TGTAGAAGTGGTTTT[A/C]CTCCAAGGAGTGGGC	84708
rs771796702	snp	C/T			intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53559910	CAAGCAATATTCCTG[C/T]CTCAACCTTCAAGTA	84708
rs771799556	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53613190	GGAAAAGGAATAAAA[A/G]GACCCCCTACACATA	84708
rs771823633	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53480602	ATAAAATGTTTTAGC[A/C]GGATATATCTGGTCT	84708
rs771836789	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53637528	ACATGTTATTTACTT[G/T]TTCACAACTCTGTGA	84708
rs771854110	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53588984	TGGTACAATGAGGCT[C/G]CAAACCAGGGGCTTC	84708
rs771879700	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53464683	TTGACACTGCTACTT[G/T]CAGAGGATAAGGGAT	84708
rs771885302	snp	A/G			intron-variant, downstream-variant-500B	LNX1, FIP1L1	GRCh38.p7	4:53463005	CCCACCTGGGAGGAT[A/G]TGTGCCCAATTTTTT	84708
rs771886442	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53547893	CGGGGGTCCTGGCAT[G/T]CATGTGCCTTTCCAA	84708
rs771897894	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53651394	GGGAACATAGTTTAT[C/T]GACATTTGTTGAAGT	84708
rs771904033	snp	A/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53520292	GAAGACCTGAGCTGA[A/T]AGCCTGGAGTGCCTG	84708
rs771904853	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53629697	TCCTGCTCTGTGTTT[A/G]TTCAATTTTTAGGGT	84708
rs771907452	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53578551	GTCTGTCATTGACCA[A/G]CATGTCGTTATGGGG	84708
rs771921486	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53486357	ATCCAGAGTAGCTGG[C/G]GCTACAGGCATGCCA	84708
rs771936334	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53607361	TGCAATCTCATTCAC[A/G]ATGGTCACGAAAAGA	84708
rs771941209	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53645955	TCAATTTCTACTCCA[A/C]GTCAGATGAGGAAAG	84708
rs771949797	in-del	-/G	1.66239e-05	0.00288299	frameshift-variant	LNX1	GRCh38.p7	4:53496340	CCTGGCAGGGCTGCC[-/G]CAGGAGACGCACAGC	84708
rs771965892	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53479009	AAAGTTTACACTTCA[A/T]AAGGAAAGAGTAAAA	84708
rs771996645	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53618278	TATGATGCAGGACTT[C/G]AGCCTTGGGAAAAGA	84708
rs772001189	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53531568	ATAAATGATTTTAGC[C/T]TGAAACTAGTTTTAA	84708
rs772010280	snp	A/C	1.76073e-05	0.00296705	intron-variant	LNX1	GRCh38.p7	4:53481860	TTTCACTGGCCTGGG[A/C]AAGAAGACACAGGCA	84708
rs772050102	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53619222	TTCATGCTTTAAAAC[G/T]TACACTTTAGTGGTT	84708
rs772071226	snp	C/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53598166	CCTTCCTGACTTCCC[C/T]AAGCAGATATTGATG	84708
rs772074629	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53583033	GGGGGGAAAATAATT[C/G]CCAAAGTTAGGGCAA	84708
rs772097288	snp	C/T	1.66183e-05	0.00288251	missense, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498649	TCTCTACCTTTAGAA[C/T]GATGTCTCCTGGCAG	84708
rs772103043	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53648891	ACAATCATGACAATC[A/G]CTATTGCCCTGAAAC	84708
rs772123545	snp	G/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53522405	GGCACCAGGCTTGGT[G/T]CTCCTATGACTCTAT	84708
rs772125906	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53494018	GCTTTTTAAAATACA[C/T]ACCCCAGGCTCCAGG	84708
rs772132674	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53563377	AGTAAACACTTGCCT[A/G]TTAGTTTTCTAAATT	84708
rs772142004	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53639594	CAAAGGCTCACAGGA[A/T]CCCAACTTCATTCTT	84708
rs772159685	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53572054	TGTATAATTGCAACA[C/T]GGGACTGTGGTGAGG	84708
rs772183052	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53466326	AAGCAGCTTTGATTA[A/C]AATTTAAATGATCGT	84708
rs772193941	snp	C/G/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53511200	TAATGTTAGCTTTCT[C/G/T]CAGTCTCTTGGCTTA	84708
rs772206486	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53627183	CAGGGAGAAGGAAAG[C/T]GTAGCTGGCTTAATG	84708
rs772211883	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53483790	TATTGGGCTAGGGGA[C/G]AAAGGTCATGAAATG	84708
rs772219387	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53551012	GAATGTTCTTGTTGC[A/G]TGAAGTCTGTGCAGT	84708
rs772239025	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53484512	AGGTTGCAGCGAACC[A/G]AGATTGTGGCACTGC	84708
rs772248975	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53562168	CTAAAATAAGTCTCG[C/T]TCAGGATCAAGAAGT	84708
rs772262556	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53647937	GATGTGGCATGTGCC[A/G]GAATTTCCTTCCTTT	84708
rs772276407	snp	C/T	3.79889e-05	0.0043581	intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573599	TGGGGGTGGGACTTA[C/T]CGGCTCGCTGATGGG	84708
rs772317581	snp	G/T	4.94654e-05	0.00497295	missense	LNX1	GRCh38.p7	4:53478718	TTACCACCTTCTCAT[G/T]ACAAGTAATTGTAGG	84708
rs772323835	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53533537	CTGAGTAGCTGGGAC[C/T]ACAGGCACATGCCAT	84708
rs772341494	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53635219	GGGTGAGGATGGGCA[G/T]AATGATACCATTAGA	84708
rs772367795	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53495088	TGTTATGACTGTTAA[C/T]GTCAATAGCATGCTT	84708
rs772373954	snp	G/T	1.64773e-05	0.00287026	missense, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498730	TGATATGGACCAGTG[G/T]GGTTTCGCTACCTCC	84708
rs772374413	snp	A/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53514650	ACAATTCAACACAAG[A/T]TTTGGGTGAGGACAG	84708
rs772377832	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53536966	ATCTCTGACTTGGTG[C/T]TAACAGTGATGATTT	84708
rs772395061	snp	A/C			utr-variant-5-prime, upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53591467	GTGAACCGAGCAGCT[A/C]CTTGGGCCGCCGGAG	84708
rs772418222	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53622112	TAAGTTATATGCTTC[C/T]CTTATTTCCCTAGAT	84708
rs772427505	snp	A/C	3.30251e-05	0.00406343	synonymous-codon, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460916	TTGATTCTATAAAAA[A/C]GTGCCAGGCCAAGAA	84708
rs772460211	snp	A/G/T			intron-variant	LNX1	GRCh38.p7	4:53481083	TAGAAGCCACAGAGA[A/G/T]AAGTACAAATTGGGC	84708
rs772467797	snp	A/G	1.71064e-05	0.00292454	intron-variant	LNX1	GRCh38.p7	4:53481697	CCCTTGCAGGAGCAG[A/G]CGACCTGCCCTAGAG	84708
rs772504944	snp	C/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53602175	AAGTTACTCTCCGAA[C/G]TGATAAGGGGATGGA	84708
rs772533928	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53500546	GTCCATTTTCCCTAA[C/T]GAATTAATAAGTACT	84708
rs772540657	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53516055	CAGGAGTTAGAGACC[C/T]GTAGCAGGACCCATA	84708
rs772592427	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53528181	GTTGGAAGAACTGTC[A/G]ATCAATCATTGGGGG	84708
rs772611948	snp	C/T	1.68029e-05	0.00289848	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508046	GCTGCCCGTCCTCTG[C/T]CGAGGACACGTAGGC	84708
rs772629393	snp	C/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53603393	AAAAGTGATGTGAAT[C/T]AGCAGAGCTGGGTTA	84708
rs772645894	snp	A/G/T			intron-variant	LNX1	GRCh38.p7	4:53476024	AAAACTGGCTGGACA[A/G/T]GGTGGCTCACACCTG	84708
rs772665431	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53515345	TGTCACCCTTTTGGT[A/G]TTCCGTTGATTGAAA	84708
rs772671012	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53557656	AGGAAAAAAAAATGC[C/T]TTATTGAGAAAGTAC	84708
rs772675576	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53534958	GAAAGAAATGATTGC[C/T]CATGGGTACAAAGAA	84708
rs772675647	snp	C/T			synonymous-codon, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573907	ATCATCCACTTCCTC[C/T]GGATAGCTGTAGAAG	84708
rs772713893	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53529372	AATTTTCCCTAGTCC[A/G]GAGAACTAGAGGCCA	84708
rs772730921	snp	C/T	0.000198396	0.00995785	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508139	GGGAGGGAGCCGTGG[C/T]TGTGAGGCTCGCACA	84708
rs772732891	snp	C/T	1.64738e-05	0.00286995	missense	LNX1	GRCh38.p7	4:53496190	TGCGCACCAGTTTTA[C/T]TCCAAGCTGCTCCTC	84708
rs772735233	snp	G/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53593667	TTAAAAAAAATAATA[G/T]GGGCTTTTTTTTTGG	84708
rs772770274	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53623686	GCTATGTTTTATTTT[A/T]GTTAAAACCACCGAG	84708
rs772788278	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53581996	TGCATTCACATTAGG[A/G]TTACTGAATTTTTCT	84708
rs772790934	snp	C/T	1.75823e-05	0.00296493	synonymous-codon, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573838	GTAGGTGTGTCCACA[C/T]GGAGTGTCCAGGGGG	84708
rs772795838	snp	A/G	1.64738e-05	0.00286995	missense	LNX1	GRCh38.p7	4:53476862	CTTCCTGGGGCTCAT[A/G]CTCTTTGACTTCCAA	84708
rs772808443	in-del	-/T			intron-variant	LNX1	GRCh38.p7	4:53550450	AGGGATCAGCAACAC[-/T]TTTTTTTTCCCCTTT	84708
rs772808582	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53643280	CTCAGTCTCCTGGGC[A/T]GCTGGGACCACAGAC	84708
rs772812839	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53495338	CATACAGGTGCTTGA[C/T]GACATTATACTGGTC	84708
rs772813822	in-del	-/T	1.65228e-05	0.00287422	utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460904	CTGACCCATCATTGA[-/T]TTCTATAAAAAAGTG	84708
rs772814928	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53547002	GCCATTTCCCTGCCT[C/G]TTCAGTGAGAGGGAG	84708
rs772863624	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53620271	CTGATATGTTCACAG[G/T]TTACAATTTTGCATT	84708
rs772886193	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53533918	GGCTATTCCAGTGCA[C/T]GCTAAGGTTTGAGAA	84708
rs772889036	in-del	-/A			intron-variant	LNX1	GRCh38.p7	4:53541148	ACTCAAAAAAAAAAG[-/A]AAAAAAAAAAAGAAA	84708
rs772915842	in-del	-/GTTTG			intron-variant	LNX1	GRCh38.p7	4:53491805	TACTTTTTTTTGTTT[-/GTTTG]TTTTTTGAGAAAAGT	84708
rs772918869	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53505450	AGAGATGGGGTTTCA[C/T]TGTGTTGGCCAGGCT	84708
rs772920583	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53517300	ATATAGTTTAAATAT[A/G]TGATAACTAATTATT	84708
rs772921833	snp	A/G/T			intron-variant	LNX1	GRCh38.p7	4:53644053	CAAAAGCAAAACCCC[A/G/T]TGGGTAGACTGCACT	84708
rs772936685	snp	C/T			intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53558552	CACCCATCACTGTCT[C/T]GACTGCACTGACATA	84708
rs772946059	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53463325	CCCTCCTGAAGCATC[A/C]ATTCAAGTTGATATC	84708
rs772963688	snp	C/T	3.29527e-05	0.00405898	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507389	CTGCACTCCCGCTCT[C/T]TGTCCTTCGAAGAAC	84708
rs772997316	snp	A/G	3.52249e-05	0.00419657	intron-variant	LNX1	GRCh38.p7	4:53481864	ACTGGCCTGGGCAAG[A/G]AGACACAGGCATTAG	84708
rs772998330	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53515078	GAGATGGGAATTAAC[C/T]GGTTGGGGGAGAAAA	84708
rs773018218	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53528428	TGTGGGCATTTTATC[A/G]CCTCATATTATCACA	84708
rs773072768	snp	C/T			intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53499481	ATTTCTTATATACCT[C/T]ATATCATGCCCATAA	84708
rs773074471	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53488969	CCTCCCACTGAGCAA[C/T]GAGTTGGAGGCTCCA	84708
rs773077265	snp	C/G	1.64808e-05	0.00287057	intron-variant	LNX1	GRCh38.p7	4:53557864	AGGCACGGACAGAGA[C/G]GGGACTCACAGTTCT	84708
rs773087356	snp	C/T	1.66139e-05	0.00288213	synonymous-codon, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461509	TTTGTTTCCATTGTA[C/T]TCTTCATAACCTCCT	84708
rs773091791	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53475935	GTCTCCAAACAAAAG[A/G]TGCTTAAACATCTTA	84708
rs773105609	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53619456	CATGCAATATGTGGC[C/T]TTTGTGTCAGACTTC	84708
rs773114435	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53556593	TGCCATTGTCTGTTT[C/G]TCTAGAAAAGCTTCT	84708
rs773124049	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53531383	GAGCCACAGTCCTCT[C/T]ATCTATAAAGTGAAA	84708
rs773150744	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53646286	ACCGGAGTGGAGTAA[C/T]AGGGCATGGTGGGGA	84708
rs773164284	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53489475	CTGAATCTGCTGGTG[G/T]CTGAGTCAGTAAAAT	84708
rs773201936	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53636517	AAGCAAATCATTTCA[C/T]CTTCAAGTATCAGGT	84708
rs773206564	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53651939	TAAAGAGCGCAAATG[A/C]CCTGAGGCCTTTCTA	84708
rs773207403	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53616934	ATAGTCATTTATAAA[A/T]GTTCCCTGACTATAA	84708
rs773207601	snp	A/G			nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53603815	ATTACATTTCAACAT[A/G]AGATTTGGGTGGGGA	84708
rs773256459	snp	A/G	3.56582e-05	0.0042223	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461408	CAACATTTAATACAA[A/G]TATTTTTGATTAGTC	84708
rs773277533	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53550967	CTGGGTTTGATTTAA[A/G]GCTCTCTTTGGGCCT	84708
rs773280070	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53467068	TGTCCCTGACCCCCG[A/C]GTAGCCTAACTGGGA	84708
rs773313169	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53637177	ATCCCAATAATTGGA[C/T]CAAAACACAACATCA	84708
rs773313418	snp	A/G	4.98186e-05	0.00499067	missense, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498651	TCTACCTTTAGAATG[A/G]TGTCTCCTGGCAGTA	84708
rs773339455	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53630371	ATACTCAGAGCAGCA[A/C]AAATTGGAGTGAAAG	84708
rs773344189	in-del	-/TTTT			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53594711	TCTTTTCTTTCTTTC[-/TTTT]TTAATTTTTTTTTTT	84708
rs773364491	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53615469	AAGCTTAGCCTAGCT[C/T]CCTCGTGTATGAGAG	84708
rs773380455	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53646888	TGTTCCAATTTAACA[A/T]GAGTAAATAAACCAC	84708
rs773386338	in-del	-/AAC			intron-variant	LNX1	GRCh38.p7	4:53543919	CAAACAAAAAAACAA[-/AAC]AATAAAAACACCACC	84708
rs773397722	in-del	-/T			intron-variant	LNX1	GRCh38.p7	4:53624880	TTTAAGATTCCAGAA[-/T]TTTTTTTACATGTAA	84708
rs773397975	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53613325	GTTTCTGTTTCACAG[A/G]TAACCTCCTGCTTTC	84708
rs773400444	snp	A/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53599520	GTCTATGGAGTAGCC[A/G]TTCTTTTATTCCTCT	84708
rs773414902	snp	C/G	5.03943e-05	0.00501942	synonymous-codon, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508047	CTGCCCGTCCTCTGC[C/G]GAGGACACGTAGGCA	84708
rs773458535	snp	C/T	1.65042e-05	0.0028726	synonymous-codon	LNX1	GRCh38.p7	4:53478728	CTCATGACAAGTAAT[C/T]GTAGGATGGAGGGGC	84708
rs773475446	in-del	-/CTGG	0.000282441	0.0118803	frameshift-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573990	GATCGTTGGCAGACT[-/CTGG]CTGGTTCATGATGGA	84708
rs773476809	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53542220	AGGAAAGTAAAATTG[A/G]GTTTCCAGAAAACCA	84708
rs773507687	snp	A/T	1.65075e-05	0.00287289	synonymous-codon, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460922	CTATAAAAAAGTGCC[A/T]GGCCAAGAAACAATA	84708
rs773512177	in-del	-/AAAAA			intron-variant	LNX1	GRCh38.p7	4:53610718	GTCTCAAAGAGGAAA[-/AAAAA]AAAAAAAAAAAAAAA	84708
rs773535994	in-del	-/TGTGTG/TGTGTGTG/TGTGTGTGTG			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53512486	TCCCTACCCAGTGTT[-/TGTGTG/TGTGTGTG/TGTGTGTGTG]TGTGTGTGTGTGTGT	84708
rs773551158	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53589104	GCCCTGGAGATAGCA[C/T]GACTGACAGCAAAAA	84708
rs773558070	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53612085	AAAGATATGAATGGG[A/C]AATATACAGAAAAGC	84708
rs773582592	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53583249	GACTCTCATGTAATA[A/G]GGAAGAATTAGGAGC	84708
rs773598951	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53524503	ACACACCCAAGTTCA[C/T]GCAGCAAGAAGGCCC	84708
rs773612204	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53553106	ATTCTGCCCTGACCT[A/G]TGCAGAAGCTGGCCA	84708
rs773629930	snp	A/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53600355	AAGGCAAAAGCCAGA[A/G]GAGAATTGTTTTGCT	84708
rs773646896	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53563784	GTGATCCACCCGCCT[C/T]GGCCTCCCAAAGTGC	84708
rs773659721	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53526048	AAAATGCAAGCCATT[G/T]TGTGAAAGACTTTGC	84708
rs773710678	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53640699	TAAGACTGTGTTGTT[A/G]TAGAAATACTGTGCC	84708
rs773712931	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53588063	CTAACTGTAAGCAAT[A/G]TAAAAATGTTTAAAA	84708
rs773717065	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53473007	GAGTGATTTTCAAAT[A/T]TTTTTGTGACTCTCA	84708
rs773745892	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53640823	ACAAAATTGTGCATT[C/G]ACTATTTCTCACAAG	84708
rs773768666	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53586654	CATGCCAAGGAACTT[A/G]GCTTTCTAGAGCAGA	84708
rs773792164	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53612192	TAAGATATGACTTTA[C/T]ACCCACCAGATTGTC	84708
rs773802579	snp	C/T	1.64738e-05	0.00286995	missense	LNX1	GRCh38.p7	4:53496193	GCACCAGTTTTATTC[C/T]AAGCTGCTCCTCGGG	84708
rs773807198	snp	C/G	3.0428e-05	0.00390039	missense, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573630	GGACCTACCTGGTTT[C/G]AAAGTGATGCTCGAG	84708
rs773818124	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53560776	AGTAATCCTGGGCTT[C/T]CTACCCTTAGACTTT	84708
rs773818208	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53485146	TATAAGCCTCCCTTC[C/T]TCTAAATAAGATTAT	84708
rs773829641	snp	A/C/T			intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53462231	GAAGTTATAAAAGGA[A/C/T]TGGGAGAAGGAAAGG	84708
rs773842071	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519116	ATGCCCAGGCTGGCT[A/G]TCTCACTGCCCCTCT	84708
rs773844620	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53624769	CATCTACCTCCTGGA[A/G]CACTGCACGTGCACA	84708
rs773868892	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53547060	CAGTTTCTTGATCTC[A/T]GTCCACCTGTGCTTA	84708
rs773886822	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53535795	ATAGTAATTCAATAG[A/T]TGAATTACTTCTCAT	84708
rs773907454	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53623727	TATCAAGAGATTTAT[A/G]TGTAGTCCTCATATA	84708
rs773908760	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53612912	AAGAAGAAATTAGTT[A/G]TGCTAGTTGACAGGA	84708
rs773923246	in-del	-/A			intron-variant	LNX1	GRCh38.p7	4:53623615	GGTAGCAAGAGTGTT[-/A]ATGATGGTATAAAAT	84708
rs773932552	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53486546	AACCTTGAGGACATG[G/T]TTCCTGCCCTCCCGG	84708
rs773954259	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53524878	CAAAAAAAGCTCTGT[A/C]TGCTTGCCCAAAGGG	84708
rs774007419	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53563653	GATTCTCCTGCCTCA[A/G]CCTCCCGAGTAGCTG	84708
rs774044936	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507588	CCTCTGGGTGGTAGG[A/G]TTGTAGAATTTGCTT	84708
rs774047248	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53495413	AGTGATCAAGAATTT[G/T]CGTCCCTCTCTTCTT	84708
rs774048121	snp	A/C			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53517768	TCACATAGCTACCAG[A/C]AACTGCACATGGAAA	84708
rs774049454	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53640875	GTTTCAGGTTCGACT[A/C]ACATGAGCTACTTTT	84708
rs774057158	in-del	-/AAT			utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460840	AAAACTGACAAGATA[-/AAT]AATATAGTGTTTCAA	84708
rs774100371	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53649467	CAGGATTTGAACTCC[A/G]GAAGTCTGGCTCCAG	84708
rs774100999	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53542784	TTGGCATTTGCAATT[A/G]CATTTAAATCTGTAT	84708
rs774105742	snp	C/T	1.66838e-05	0.00288818	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507288	AAGCCCAGCCCATGT[C/T]CATCCAGCCTTATGG	84708
rs774115439	snp	C/T	1.64743e-05	0.00287	synonymous-codon	LNX1	GRCh38.p7	4:53476857	GCAGTCTTCCTGGGG[C/T]TCATACTCTTTGACT	84708
rs774124681	in-del	-/A			intron-variant	LNX1	GRCh38.p7	4:53560290	GATACATCTTTTATT[-/A]AAAAAGGATGACTGC	84708
rs774129196	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53582247	GTGCCACTAAACTTC[A/G]CCCAAGGTCAGAATT	84708
rs774130905	in-del	-/TT/TTTTTT			intron-variant	LNX1	GRCh38.p7	4:53636179	CACATCTATTACTCC[-/TT/TTTTTT]TTTTTTTTTTTTTTT	84708
rs774158159	in-del	-/A			intron-variant	LNX1	GRCh38.p7	4:53474304	ATATAAACACAGGCC[-/A]GGGGTGAGCAATTTA	84708
rs774162598	snp	A/G	1.64776e-05	0.00287028	missense, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498780	CTTTCACTGGGATCT[A/G]CTCGATTGATCTTGA	84708
rs774180044	snp	A/G			intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53558635	CGAGAAGAATAGGCT[A/G]TGCCATTCTCTGTCA	84708
rs774187110	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53490633	AAAAAGCTGAATGTG[C/G]GGTACTGTGGGAGAG	84708
rs774226523	in-del	-/A			intron-variant	LNX1	GRCh38.p7	4:53628480	CATTATTAAGAGGTC[-/A]AAAAAAACAGTAGAA	84708
rs774247132	in-del	-/GTT	1.65056e-05	0.00287272	cds-indel, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460937	GGCCAAGAAACAATA[-/GTT]GTTAGAGTAATTCTT	84708
rs774250939	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53521521	TTTGGAAACGTGTCA[C/T]GCAAAGATAGCTGGT	84708
rs774294063	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53637845	AGACTAGGCTGCTGA[C/T]GGAGATTAGACCACC	84708
rs774302587	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53557758	GGTGCTTTGTCCAAG[C/T]GCATCTAGTATGTGT	84708
rs774312970	snp	C/T			intron-variant, utr-variant-3-prime	LNX1, LOC101928879	GRCh38.p7	4:53576990	GGCAAATGCCCTTAA[C/T]ATAAAAACATTTAGA	84708
rs774329248	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53647763	TAAACAGTAACTCTC[C/T]ATTCTCCCTTTCCCT	84708
rs774339088	in-del	-/GAT	1.69937e-05	0.00291488	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461063	AAAAAAACAAAACAA[-/GAT]GATATGATTAGTATT	84708
rs774346728	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53626253	GGGGTGGGAATAGAA[A/G]AAGATCACAAATTGG	84708
rs774351314	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53464887	GTCAAATTTAAATTA[G/T]CTCTCAGTGACATGA	84708
rs774362460	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53644074	AGACTGCACTTACTA[C/T]GTTTTGTACTTCATT	84708
rs774378500	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53617048	TCATATAAGTCTGTG[C/T]TTGTGCCAGTTACTA	84708
rs774392825	snp	C/T			intron-variant, nc-transcript-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53500502	CTGCTTCTAGTTCCT[C/T]GTGAGCATTTTCAAA	84708
rs774393528	snp	A/C			upstream-variant-2KB	LNX1	GRCh38.p7	4:53653215	ACTAAGTCATTCCTG[A/C]AAAGTGACCCAGCTA	84708
rs774408805	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53482682	GGCAGAGTAATATAA[C/T]GGACTTTGGAGACTC	84708
rs774409896	snp	A/C/T	3.35375e-05	0.00409485	missense	LNX1	GRCh38.p7	4:53481730	CTCACCTTGGGAGTG[A/C/T]TGCTCCTCTCCCCTG	84708
rs774421003	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53465211	CTGCCCAGTTTACAT[A/C]TTTAAAAAGTTGGGA	84708
rs774422395	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53489008	ACTCTAGAATGAATT[A/T]ATGGTGTACTATAAG	84708
rs774425232	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53483688	TAAGGTTTGGTGGTT[C/G]CTCTCTTCATCCCAT	84708
rs774448453	snp	G/T			upstream-variant-2KB	LNX1	GRCh38.p7	4:53654071	TTACACTTGAGGTTG[G/T]TCAGCTTTTTGTTCT	84708
rs774451900	in-del	-/CGCCTGTAATCCCAGCACTTTGGGAGGCCG			intron-variant	LNX1	GRCh38.p7	4:53549489	TTAAGAGATGTGGCA[lengthTooLong]ACTAATTGCAACGTG	84708
rs774476329	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53511406	TTCAAAGCAAGGAGG[A/G]TTTATGCTTCCTTTC	84708
rs774492276	snp	G/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53600875	AGCTGGGATTACAGG[G/T]GCCCACCACCACACC	84708
rs774492978	snp	A/T			upstream-variant-2KB	LNX1	GRCh38.p7	4:53654497	CGGATTAGCACTGAT[A/T]GATTTGGTTCCAAGA	84708
rs774494085	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53490681	TGTTGTCTGGGAATT[C/T]CTTTGTAAGGCAAAT	84708
rs774497649	snp	A/G	1.65329e-05	0.0028751	synonymous-codon, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460988	TCTTGCCAAGCAAGC[A/G]TGTATCATTCCTGAT	84708
rs774499743	snp	A/G	1.66746e-05	0.00288739	synonymous-codon	LNX1	GRCh38.p7	4:53481801	CTGAAAGATGTCAGG[A/G]CTCCGCTGCCGAACC	84708
rs774504452	snp	C/G	3.28931e-05	0.0040553	intron-variant	LNX1	GRCh38.p7	4:53496423	GAACAATCGTGCGGT[C/G]AGCTCCACCTGCCAC	84708
rs774577202	in-del	-/C			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53515509	ACTTCAATTTAAGGC[-/C]CCCACCCCACCAAAA	84708
rs774587176	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53578982	AGCTTATAAACATGT[A/G]TGATGTATCACGTTT	84708
rs774595645	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53635131	CATGGTGCCCAGCCC[A/C]TCTCTGCCTTTTTGA	84708
rs774601042	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53607997	ACTTAAATATAAAAC[C/G]TAAAACTTTAAAAAC	84708
rs774607768	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53492174	AAAGTGTATATGAGC[A/T]GAAATGGACACAATT	84708
rs774623288	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53579880	CAACGATAATTTTAC[A/G]TGTTCTTCCCATTGA	84708
rs774626938	snp	A/C	1.64743e-05	0.00287	missense	LNX1	GRCh38.p7	4:53478629	GATGACATAGATAGG[A/C]AAATCCCATTCTCTA	84708
rs774643585	snp	C/T	1.64833e-05	0.00287078	missense	LNX1	GRCh38.p7	4:53478706	CTTTTTGGATATTTA[C/T]CACCTTCTCATGACA	84708
rs774649673	snp	C/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53602068	CTTCTTGTCAGTTAG[C/T]CTTATGGTTCTACTG	84708
rs774652664	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53572559	AAAAAATACCTGCAC[C/G]TGCCTCTTGCCCTTG	84708
rs774748644	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53473768	GACATGAGTTTACCT[A/G]TATAACAAACCTGCA	84708
rs774758669	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53487325	CCAGCCAAAGGCTTC[A/T]CCTGCTCATTGGCAG	84708
rs774813213	in-del	-/TG			intron-variant	LNX1	GRCh38.p7	4:53475721	GAGCAAACACCAACT[-/TG]TCTGTTCTTTGAATA	84708
rs774820461	in-del	-/G	1.65861e-05	0.00287972	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507474	AAAGGGCCGTGCTGA[-/G]GAATAGCGACAGGAG	84708
rs774830435	snp	A/G	6.71051e-05	0.00579207	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507495	GCGACAGGAGGAACA[A/G]TAGTTATGATTTAAT	84708
rs774857885	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53542290	ACAGACAAATTCATG[A/C]GATTATCTTAAAGAT	84708
rs774868079	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53497702	CCACTAGAACTGGGA[A/G]GCAGCAGTGCACAGT	84708
rs774889671	in-del	-/A			intron-variant	LNX1	GRCh38.p7	4:53607273	AAAGTTTCAGGGTAC[-/A]AAAATCAATGTACAA	84708
rs774913053	in-del	-/AAC	1.79462e-05	0.00299546	intron-variant, cds-indel	LNX1, FIP1L1	GRCh38.p7	4:53461391	CTTTGGCATTTATGA[-/AAC]AACATTTAATACAAG	84708
rs774917458	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53487731	ATGCGACTGATAACT[A/G]TATAAGCTGCTTATA	84708
rs774927659	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53542378	CTGAATGCGCAGTGT[C/T]TTGGGATTTTATATT	84708
rs774939356	snp	G/T	1.74854e-05	0.00295676	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507941	CCACAGAGGGCAATC[G/T]CAAGCCAAGGAGCCC	84708
rs774973030	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53473119	AAAGAAAATTGATAA[A/C]CAACCATATTACTAT	84708
rs774983737	snp	A/C	1.6486e-05	0.00287102	stop-gained	LNX1	GRCh38.p7	4:53496073	ATCGAAGATCATGTC[A/C]ATTGATGGCTAACAC	84708
rs775007292	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53488772	CCACATGATGCCATA[C/T]AGACCTTACATGACA	84708
rs775009641	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53613822	CCTTTGGGTATATAC[A/C]CAGTAATGGGATTGC	84708
rs775012373	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53526213	CTGGACACGGCACAC[C/T]GCTCCCTGAACACAT	84708
rs775042592	snp	A/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53605509	TTGTAACTATAATCT[A/G]CATGCTGTACTTTAG	84708
rs775050448	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53642161	CAAAAGGTTGAGGCT[G/T]CAGTGAGCCATGATC	84708
rs775061672	snp	C/G	1.68142e-05	0.00289945	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508041	TGCTGGCTGCCCGTC[C/G]TCTGCCGAGGACACG	84708
rs775095614	in-del	-/ATC			intron-variant	LNX1	GRCh38.p7	4:53530689	AAAACTTAAGTATGT[-/ATC]ATCTAAGTAAATGTC	84708
rs775116057	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53554464	TGTTTTGTTTTAAAT[A/T]GAATTTGAATGCTTT	84708
rs775125628	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53650996	AAGACAACGCTATGA[A/G]GGATGTATTACCATC	84708
rs775129661	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53537553	TGGACATTTTTTATG[C/T]TCCTTTAGTATTTTC	84708
rs775155138	snp	A/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53595934	CCACAATTAAAATGG[A/G]CATATTCCATTTGAC	84708
rs775207621	snp	C/T	1.64953e-05	0.00287182	intron-variant	LNX1	GRCh38.p7	4:53476742	TACAGGGATGTTGTG[C/T]TTGGACTTACCGTGG	84708
rs775235157	snp	C/T	4.84707e-05	0.0049227	missense, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573680	TGGGTGCAGTGCTCC[C/T]TGAATGGGCAGGTCA	84708
rs775236837	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53626113	ACCTGGAGACTATTA[G/T]GCTAAGTGAAAGAAG	84708
rs775258232	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53484347	GCAGGCAGATCACTT[A/G]AGGTCAGGAGTCCAA	84708
rs775296172	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507853	TTGGCGAATTGGACA[C/T]TGGGTTCCTGCCAAA	84708
rs775304160	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53548031	TTCCAATCTTGGTGG[C/T]AATGAAAGCAGGTGT	84708
rs775313862	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53572609	AAACAACATCTTCCA[A/G]ATTTCCTCTTACAAA	84708
rs775333558	in-del	-/ACAC			intron-variant	LNX1	GRCh38.p7	4:53636751	CTCCCTTTTCATCTT[-/ACAC]ACCCAATTAGCTGAT	84708
rs775340665	snp	C/T			intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53558892	GCCACATCCCCTCTT[C/T]CAGCTTTAAGATCTG	84708
rs775353686	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53480623	TATCTGGTCTGTCTA[A/G]ACTCCTTATTGTAGA	84708
rs775366972	snp	A/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53520381	TGTGGAGTTGACAGT[A/T]GTTAATGAGGGATGG	84708
rs775367047	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53503368	TTTCTTAAATAATGA[A/G]ACTTAAAAGTAGAAA	84708
rs775409813	snp	C/T			intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53462454	GCTGTAGTCCGGGAA[C/T]TGGTTTGAAAGGAAA	84708
rs775430609	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53547138	TGTCTATTGTGAGGC[A/G]CACCATTATTTTTAC	84708
rs775432639	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53466608	GAAAGGGGTGACAGA[C/T]GGCACCTGGAAAATC	84708
rs775460198	snp	C/T			intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53499543	GGTTCTCTGCATATA[C/T]CTCTGCATGCAGAGG	84708
rs775482068	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53486764	TTTTGTTTAATGACT[A/G]CTTTTCTCTGTTGAG	84708
rs775490837	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53615590	GCTGAATGAAAACCC[A/G]TAGAGGAAGAGCTTA	84708
rs775541376	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53639610	CCCAACTTCATTCTT[A/G]CTAAGTAGAATGGAC	84708
rs775546792	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53530287	TAGAAAAAATATTGC[A/T]AGATATGTAATCAAA	84708
rs775579877	snp	C/T	1.64942e-05	0.00287173	synonymous-codon, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508173	GTCTGGACAGCCATC[C/T]TGTGAGCGCCTCTTC	84708
rs775580394	in-del	-/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53511344	AAGCGGGGAAGAGCT[-/G]ATTAGCATTGGCCAG	84708
rs775595347	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53475266	ACAAAATAATTTTAA[C/T]AGATCCTAGTTTCAG	84708
rs775596248	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53627893	AGATGAGGGTTTCAA[C/T]GGGATGAATGTTAAG	84708
rs775601059	in-del	-/ATA			intron-variant	LNX1	GRCh38.p7	4:53570662	AAAACTTAAAGTATA[-/ATA]ATAATAAATAAATAA	84708
rs775618885	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53619246	AGTGGTTTTTAGTTT[A/C]TTCACAAGACTATAC	84708
rs775629287	snp	A/G	3.29821e-05	0.00406078	intron-variant	LNX1	GRCh38.p7	4:53557826	CGGGTCCCACCCCCA[A/G]CATACTAGGCACATA	84708
rs775634773	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519200	GAGGCCTAAAAGGAT[C/T]TTGTCTAAGTGTGCG	84708
rs775636773	snp	C/T	0.000148284	0.00860929	missense, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498739	CCAGTGGGGTTTCGC[C/T]ACCTCCCACCAGCCT	84708
rs775655991	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53629909	TATGCACAATAAAGA[C/T]AACAATACATCAATT	84708
rs775657173	snp	C/T	1.79348e-05	0.00299451	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461396	GCATTTATGAAACAA[C/T]ATTTAATACAAGTAT	84708
rs775664006	snp	A/C			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53521715	GGAAAGGAGGGGATG[A/C]TTTTCCTGTTTGCAG	84708
rs775675588	in-del	-/A			intron-variant	LNX1	GRCh38.p7	4:53651638	GGGAATGGAGACAGG[-/A]TGTGCTGCTGGTCAC	84708
rs775679150	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53580028	GTGTGTCCTGCATTG[A/G]CACTTTAACCTTGTC	84708
rs775713534	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53562273	GGCCCCACTACACAC[C/T]GGTAATGGCCTCCAG	84708
rs775735059	in-del	-/G			intron-variant	LNX1	GRCh38.p7	4:53544913	CCAGGCTCTAACTCT[-/G]GAGTCCCGCTTGTGA	84708
rs775736401	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53642555	AGTCATATGTGGCAC[C/G]GTTATTCTTTATATG	84708
rs775736457	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53482797	AATCTCAGACTTCAC[A/C]ACCATACAATGCATC	84708
rs775749256	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53539123	TAAAATCAGATCAGC[C/T]GTGTAATCACCCTGC	84708
rs775753343	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53551514	AATCCTCAACTGATA[A/G]GGAGAAAAAGCCCTC	84708
rs775754221	snp	C/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53597269	TCAATTGATATTCCT[C/G]ATCTTTTCAGTAGTC	84708
rs775762433	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53533600	GGATGAGGTTTCACT[A/G]TGTTGATCAGACTGG	84708
rs775794557	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53532921	TCCTCCTCTGGGAGC[C/T]TGCTAGGCTGATGCT	84708
rs775840416	in-del	-/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519440	AGTTTTGTTCAGTGT[-/T]TTTTTTTTTTTTTTT	84708
rs775875823	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53551080	GTTAACCTAGGAGGC[C/G]GTTGGTGGTTGGAAT	84708
rs775894519	in-del	-/C			intron-variant	LNX1	GRCh38.p7	4:53614579	GTTCCATCACAGGTA[-/C]CCAGGAAAATGACCA	84708
rs775928850	snp	G/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53504680	TCATTTCTAGTTTTT[G/T]ATTTAAAGTGAGAGA	84708
rs775931210	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53621007	CAATATGATAGCATG[A/G]CTTTCAAACATTTTA	84708
rs775953250	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53590410	CGCAGATTTATTTCT[A/T]TTTCCAGTTTTTCCA	84708
rs775966795	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53648019	TCACTGGACACTTGG[A/G]TTGCATGTACCTTTG	84708
rs775977447	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53647382	GGAAGCAATCTCTCT[C/T]TCTCTTTTTCTCCCT	84708
rs775988328	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53586483	TGCCTGTGACAAATG[C/T]GTCAAACACAAGAAG	84708
rs776016745	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53494122	GCTCCCATCATTCCC[A/T]TGTGTTGTGGGAGGG	84708
rs776023444	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53475374	TTTAAACTGACTCAA[C/T]GCTCAGATTTTAACT	84708
rs776036171	snp	A/C/G	6.58984e-05	0.00573983	missense, synonymous-codon	LNX1	GRCh38.p7	4:53478623	AACACTGATGACATA[A/C/G]ATAGGCAAATCCCAT	84708
rs776053580	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53622270	GCATTTGCAATAAAT[C/T]CAACTTTGTTCTGAG	84708
rs776062895	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53543439	TTGTTATTAAATTAT[A/G]CTCTTCCCAGGAATG	84708
rs776080216	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53584538	GTTAATGGGATAGAC[A/G]GTCCTTGGGAAGGAT	84708
rs776083798	snp	C/G/T			intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53574136	CCCAGCACATGAAAG[C/G/T]CTTATGCTTATGGTA	84708
rs776111028	in-del	-/T			intron-variant	LNX1	GRCh38.p7	4:53586890	TGGGTATTCAACATG[-/T]TTTTTTCATTTAATC	84708
rs776113435	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53643970	ACTCAGCCACAGTTG[A/G]TGTACATTTTTATTA	84708
rs776114354	snp	A/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53602546	GGTGGCTTTTAGAGT[A/G]CAGCCACTTGAGTCC	84708
rs776122418	snp	A/G	3.29712e-05	0.00406011	stop-gained, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507416	GAACACTCAAAGCTC[A/G]ATTTATTTTTTTAAA	84708
rs776123461	snp	C/G	3.29625e-05	0.00405958	synonymous-codon	LNX1	GRCh38.p7	4:53476764	TTACCGTGGTAATTC[C/G]AGCCACATGACCCAG	84708
rs776125578	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53561092	TTTAGGGGCCAGGAA[A/T]ATGTTGGGTTCAGAG	84708
rs776152363	snp	A/G	1.6486e-05	0.00287102	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507325	CATTTACCTTCAGGG[A/G]CAGTGGTGTTTTCAG	84708
rs776154926	snp	A/G			nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53603659	AGGAGCAAGAGAGGC[A/G]CGGGGAGAGGTTTTA	84708
rs776164638	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53633184	TTGCAAGGATATTGT[A/G]ATGATCACATTAAAT	84708
rs776169392	in-del	-/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53506892	AGGAATAATAGTAGC[-/T]ACCTCATAGGGTTGT	84708
rs776197093	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53503627	CCATGGAGAAAGCAC[A/G]GGCAGAGTAGATTTA	84708
rs776197869	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53631901	TCCTTGACTCGGTGT[A/G]ATTCTATAGTTGTTA	84708
rs776199325	snp	C/T	1.90842e-05	0.00308897	utr-variant-5-prime, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53574048	TCAGTCACACAATAT[C/T]TCCTCAGGAGCAAGT	84708
rs776201886	in-del	-/T			intron-variant, frameshift-variant	LNX1, LOC101928879	GRCh38.p7	4:53576181	GTTGCTGACTTTCAG[-/T]GGTGGGTGGATGTGA	84708
rs776207255	in-del	-/T	6.82576e-05	0.00584159	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498591	GTTTGCTCAGAAGCA[-/T]TTTTTTTATATCAAG	84708
rs776208259	snp	G/T			upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53591751	CCTGAGCACAGCACG[G/T]GTCCAGCCCCGTGTT	84708
rs776251678	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53527162	AAATATTCAGTTTTC[G/T]GTTCTCAGCACCAAC	84708
rs776252612	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53623841	ATAGCTTGCCCAAGG[C/T]TGCACAGTAAATGAG	84708
rs776297198	in-del	-/TGTGTGTATGCGTG			intron-variant	LNX1	GRCh38.p7	4:53641075	CAGGCTACTGCTCTA[-/TGTGTGTATGCGTG]TGTGTGTATGCTTGT	84708
rs776316329	in-del	-/ATT	3.37359e-05	0.00410692	intron-variant, cds-indel	LNX1, FIP1L1	GRCh38.p7	4:53461424	TATTTTTGATTAGTC[-/ATT]ATTATTACCTAATTC	84708
rs776321921	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53544575	TGAGTAGAACCCAAG[A/G]AGGCCAAAAGGTGGG	84708
rs776388287	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53615251	GGTTTCTTATGCAGC[A/G]GTAGTTGGCGAATGC	84708
rs776400399	snp	C/T	1.72442e-05	0.00293629	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461616	AGAATGTAATCAGTG[C/T]ACATGCATATTTAAG	84708
rs776430889	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53546619	TAGTTTCTTCATCTA[C/T]AAAATAGGGGGATTA	84708
rs776434106	snp	A/G	1.66125e-05	0.00288201	synonymous-codon, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461527	TTCATAACCTCCTAC[A/G]ATGCAGAAGCCCAGA	84708
rs776440678	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53588969	ATGAACCTCCTTCTA[C/T]GGTACAATGAGGCTC	84708
rs776445989	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53584802	CTTCTATCTGAAACA[C/G]TTCCACTGATGGAGA	84708
rs776480989	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53463487	CTGACTTTGTGGGCA[C/T]TTTTTTCTTAAGTTG	84708
rs776497007	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53631840	ATCAATTCAGAGTCT[C/T]TTTGGAGGTGGAGCC	84708
rs776513621	in-del	-/AAG			intron-variant, nc-transcript-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53523207	TTTATGTTCCTGACA[-/AAG]AATAAGGATTGTTAT	84708
rs776524670	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53488049	CTGGTTCCATAAAAT[C/T]AGAAAGTCACAGACA	84708
rs776527783	snp	A/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53596078	TTTTTAAATGGGCTC[A/G]GCTCCATATCTTTTA	84708
rs776528128	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53464746	AAAAGACAATCTCAC[A/G]TAGAAATGTTCAGGA	84708
rs776534442	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53541982	CCAGATGACACATGG[C/T]CCTGGGGAATAGAAT	84708
rs776551037	snp	G/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53594977	TCGGCCTCCCAAAGT[G/T]CTGGGATTACAGGTG	84708
rs776564899	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53536884	TGATACAAATATTTT[A/C]GTATAGATGTAGAAT	84708
rs776567276	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53472916	TAACCCTACCAGTAA[G/T]AAGAGAATAACTGAG	84708
rs776585877	snp	G/T			intron-variant, utr-variant-3-prime	LNX1, LOC101928879	GRCh38.p7	4:53577125	CTGATTGTCCTCAAG[G/T]CTGTTAGAAAGTACT	84708
rs776591132	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53482466	AACTTAAGTGCCCAT[A/C]AACTGATAGGTAGAT	84708
rs776593957	in-del	-/AAG			intron-variant, cds-indel	LNX1	GRCh38.p7	4:53558135	AAATCACGGGCCCGT[-/AAG]AAGATTATGCTCTCT	84708
rs776610041	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53490749	AAGGATTGGTTAGAA[A/G]TTTGAGTCTCAACAT	84708
rs776621564	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53614238	CATTTGCCACCCTGT[A/C]CCTACATATTCTCCA	84708
rs776628044	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53617253	GAGACCTCACCTTTT[C/G]CAGGGAAGAATCTGA	84708
rs776629642	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53626993	ATTATAAAGATTGGC[C/T]GGGGATCCCAGTTTG	84708
rs776638075	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53500618	TATGTTAGGGCAAAG[C/T]AACTTAGTGGGCAGA	84708
rs776647304	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53549187	GTAAAAAAAATAAGT[C/T]CTCCCCTTAAAGCTT	84708
rs776710639	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53520886	AGAATCACTTGAACC[C/T]GGGAGGTGGAGGCTG	84708
rs776723714	snp	C/G	1.69035e-05	0.00290714	intron-variant	LNX1	GRCh38.p7	4:53481713	CGACCTGCCCTAGAG[C/G]CCTCACCTTGGGAGT	84708
rs776736933	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53640544	TTTCATTGCTAAAAA[A/T]AAAGAATCAAAAGTG	84708
rs776757313	in-del	-/A			intron-variant	LNX1	GRCh38.p7	4:53625009	AAATTCAATTGTTTT[-/A]AAAAGATTTATATAT	84708
rs776769431	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53551482	GAGGCAAAATGGCAG[A/C]GTTTAACTGGTATAT	84708
rs776777536	snp	C/T	1.65061e-05	0.00287277	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508159	AGGCTCGCACAGCCG[C/T]CTGGACAGCCATCTT	84708
rs776777903	snp	C/G/T	5.61722e-05	0.00529939	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461085	ATTAGTATTTTAATT[C/G/T]GTTGCTGAAGTTAAT	84708
rs776778107	snp	G/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53509236	CAGAAATCATATCAC[G/T]AGCCCCTTTAGGAAG	84708
rs776778607	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53649753	GGGCTAGGTGCCCTC[C/T]GATGGCAGGCTGTGT	84708
rs776788185	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53615803	AGGTGCATATATTTA[C/T]GGGGTACATGAGATG	84708
rs776810937	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53588003	CCTCAACGTACTACC[A/G]TTTCCATCATTATTA	84708
rs776814929	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53529661	GTACATTGTGAGCTC[C/T]CAGAGTGTGAGAGAG	84708
rs776822973	in-del	-/T			upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53593128	GGAGGTAACAAAACC[-/T]TTTACACTCAGGTGT	84708
rs776879628	snp	A/T	4.95209e-05	0.00497574	missense, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460945	AAACAATAGTTAGAG[A/T]AATTCTTCCTTTAAG	84708
rs776891512	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53524319	CCAAAGGCCCAGGCT[C/T]GGAGGTGGCAGAAAA	84708
rs776899127	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53584040	TAGGAGTCACCAAGG[A/G]TCCCGGGAAGAGCTG	84708
rs776926389	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53540639	GCGAGCCGAGATTGC[A/G]CCACTGCACTCCAGC	84708
rs776981300	in-del	-/AG			intron-variant	LNX1	GRCh38.p7	4:53527071	AAAAAAAAAAAAAAA[-/AG]ACTAGAAGAACAAAA	84708
rs776990721	snp	G/T			upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53593154	GGTGTTTCAGGAAAA[G/T]GTTTCACGCCACTAG	84708
rs776996424	in-del	-/A			intron-variant	LNX1	GRCh38.p7	4:53637353	ACCAACCACTGCTTG[-/A]AAAAAAATCTAATTA	84708
rs777009315	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53533764	GGGGGTAGAGGACAG[A/G]GATACTGCTAAACAT	84708
rs777014617	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53549607	CTCACATTTCTTAAG[A/G]ATCTATCTTTAGAGA	84708
rs777031736	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53622445	CTCAGCACACATGAA[A/G]TGTGTCAACCTGATT	84708
rs777061332	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53562477	TAGTCTGAAGACAAT[C/G]AATGATCTAGCCAGT	84708
rs777062569	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53506292	ATTGTCACATCTAAA[C/T]GACTTAAAACACTAT	84708
rs777081494	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53611200	TAGCTTTTTTGTACT[C/G]TAGGAATAAGAAAAG	84708
rs777121950	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53606711	AAAAATCCTCAATAA[A/G]ATACTGGCAAACTGA	84708
rs777134447	in-del	-/TGAGACAGAGTC			intron-variant	LNX1	GRCh38.p7	4:53474784	TTCTTCTTTTTTTTT[-/TGAGACAGAGTC]TCTCTCTGTCACCCA	84708
rs777147482	snp	C/G	1.6654e-05	0.00288561	missense	LNX1	GRCh38.p7	4:53496346	AGGGCTGCCGCAGGA[C/G]ACGCACAGCGTAGTT	84708
rs777155899	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53562854	CATTTCACAATATAT[A/G]CATATTTTAAAACAT	84708
rs777165622	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53505014	CATGAAGTGAGCACA[C/T]GCTTTTGGAAAAATG	84708
rs777205881	snp	C/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53598363	TCAGCCTCCCAAGTA[C/T]CTGGGACTACAGGCA	84708
rs777210139	snp	A/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53605424	AACTACCTTGTGTAT[A/G]CGTGTATGGGGGTGG	84708
rs777213155	in-del	-/TAGTT			utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460720	CTGAAAAAAAACTAG[-/TAGTT]TAGTTTTAATTTTTT	84708
rs777247364	snp	G/T	1.73576e-05	0.00294593	missense, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573853	CGGAGTGTCCAGGGG[G/T]TCCAGCAAAGCCTGC	84708
rs777250528	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53465803	GTTATGAAACATAGT[A/G]CCCTTTTTACCACAG	84708
rs777267102	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53545672	TGCATTTAATTCTTA[C/T]CCCCATGAGGTAGGT	84708
rs777274201	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53526206	CCCATCACTGGACAC[A/G]GCACACTGCTCCCTG	84708
rs777316663	snp	A/G	1.64784e-05	0.00287035	intron-variant, synonymous-codon	LNX1	GRCh38.p7	4:53557909	CAGGTTGCCCACATT[A/G]TCAATGTAGTTAGCA	84708
rs777323532	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53635948	AGTGTGGGCTGATAC[A/G]GCCAGTGATGGGGAA	84708
rs777339056	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53494260	GACCCTCATTCTCTC[C/T]TGCCTGCTGCCATGT	84708
rs777344849	snp	A/C	3.31285e-05	0.00406978	intron-variant	LNX1	GRCh38.p7	4:53477008	AGAAGCAGAAGCTAT[A/C]TTTAGTGAGAGCACA	84708
rs777360870	snp	C/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53512007	CTTGGTTCACTGTTG[C/G]ATTAGCAAACATTGA	84708
rs777373288	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53627838	AGAAACCCTCCTCAT[C/T]AGCCAGTTCTCCTTC	84708
rs777389308	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53540510	ACATGGTGAAACCCC[A/G]TCTCTACTGAAAATA	84708
rs777401582	snp	C/T			intron-variant, utr-variant-3-prime	LNX1, LOC101928879	GRCh38.p7	4:53576515	TTCATCCAGGTGCTT[C/T]TGTAGATCTTGTATT	84708
rs777429146	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53607244	AAAGCTCACTGATCT[C/G]ATAAACAACTTAGCA	84708
rs777462181	snp	A/T	1.70874e-05	0.00292291	missense, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573946	CTCCAAGGAGTGGGC[A/T]TGGCCACACACTGCA	84708
rs777516959	snp	A/T	1.804e-05	0.00300327	utr-variant-5-prime, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53574008	GCTGGTTCATGATGG[A/T]TTGGAGAGCAGTATA	84708
rs777517173	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53466702	TATATCCCGCACCTG[A/G]CTCGGAGGGTCCTAT	84708
rs777517324	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53485732	GCTGGATTCAATGCA[A/G]AGAAACATCCCCTAG	84708
rs777529172	snp	A/G	5.62203e-05	0.0053016	intron-variant	LNX1	GRCh38.p7	4:53496400	TCCCGTTGACCTGGG[A/G]GCAGGTGGAACAATC	84708
rs777533198	snp	A/T	1.65034e-05	0.00287253	missense	LNX1	GRCh38.p7	4:53476965	TTCGACCCCATCCAC[A/T]TTCAACAAAATGTCA	84708
rs777544600	in-del	-/AGAG			intron-variant	LNX1	GRCh38.p7	4:53549477	GTTGAAAGAAACTTA[-/AGAG]AGAGATGTGGCAACT	84708
rs777544869	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53530052	GATATGTTTTATCAA[A/G]TAAAAATTAAATACT	84708
rs777562147	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53587801	GGAAATCACCGCTCC[A/G]GGAAGACCCGCTGTT	84708
rs777596102	snp	A/G			upstream-variant-2KB	LNX1	GRCh38.p7	4:53653440	AGAGATGTGAGTCGG[A/G]TGCTGGATGTTATCT	84708
rs777603571	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53639559	GTTATTTATTGATTG[G/T]CTGATGAAAATGGTG	84708
rs777606776	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53490425	AAAAATAAAATTGTA[C/T]TTAGTAGCTACATAA	84708
rs777610775	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53546284	GGACCCAGGCTGCAC[A/G]TGTTCAAAATTGGTC	84708
rs777620203	snp	A/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53600440	GTTTTCCTTCCCAGG[A/T]ACTTTTGCTTCCAAG	84708
rs777643709	snp	A/G	3.31741e-05	0.00407259	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507472	TCAAAGGGCCGTGCT[A/G]AGGAATAGCGACAGG	84708
rs777644108	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53484494	CTTGAACCCAGAGGG[C/T]GGAGGTTGCAGCGAA	84708
rs777644927	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53513264	TTGATCTTTTTTAAT[A/G]TATTATGCTTTATGG	84708
rs777648524	snp	A/G	1.64749e-05	0.00287005	missense	LNX1	GRCh38.p7	4:53476814	GTGGGGCCATGTTGT[A/G]GTTGGAGTCCAGGGC	84708
rs777650550	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53503398	ATTACTCTTTGATCC[A/G]CGGGCTGCAGAATGG	84708
rs777666320	snp	A/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53511045	AAGGAAAACCTCATA[A/T]GGTAGGTAAGTAGCC	84708
rs777691821	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53628629	CCCACTGTTGGGTAC[C/T]TACCCAAAGGAAAAG	84708
rs777695081	snp	C/T	1.68761e-05	0.00290478	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508007	TTCGGTTGCTCCGGC[C/T]AGAGTCCACTGGGCT	84708
rs777704316	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53621845	GGTGCCAGCCAGTGG[C/T]AAATTGCTTTGGACC	84708
rs777708029	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53608236	TACAAATGTCTAATA[C/T]CCAGAATCTATGAGG	84708
rs777720951	in-del	-/TTTTT			intron-variant	LNX1	GRCh38.p7	4:53545804	CTTCAGAGGCCACAT[-/TTTTT]TTTTTTTTTTTTTTT	84708
rs777733110	snp	G/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53500407	GCTGAGATGCTTCTG[G/T]CTTCCGTAGGTGCTG	84708
rs777738535	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53639750	ATCAAGAGTTATTTA[C/G]GTCAGGTGTAGTGGC	84708
rs777747033	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53536096	GCTGCTTTGCCATTG[C/T]TTTGTTCATTATTCC	84708
rs777763192	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53585941	GGTGAATGCTCCCAA[C/G]GATCCTTTCCAACAC	84708
rs777783235	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53632418	ACACCTGCCTTCTGC[C/T]AAATAGCTGCTCCCT	84708
rs777786863	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53544235	AGTCTCACTCTGTTG[C/G]CCAGGCTGGAGTGCA	84708
rs777810241	snp	A/G	1.64773e-05	0.00287026	synonymous-codon, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498731	GATATGGACCAGTGG[A/G]GTTTCGCTACCTCCC	84708
rs777816271	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53488416	TCCTAGTTTTTTCCA[C/T]ATTAAATATCTTTTC	84708
rs777830796	snp	C/T	1.66056e-05	0.00288141	missense	LNX1	GRCh38.p7	4:53496051	GCCGCACTTTCTGGG[C/T]TGCCATATCGAAGAT	84708
rs777842688	snp	A/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53601984	GCTCACGTGACTGAC[A/T]TCTCCAGTCAGCACC	84708
rs777850983	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53573191	CACTTAGAGCAGTCA[C/T]ATCCATGGAGACAAA	84708
rs777853216	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53631351	GAACTTCCCTGTGGG[C/G]CTTCAGCAGAAAGAG	84708
rs777866075	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53477097	CAGAGAGGGCAAAGG[C/T]TTTCTTTGTTGACGG	84708
rs777866240	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53564436	AGTCCTGGATGAGGG[G/T]ATGAGGAGGAGTGGC	84708
rs777894121	in-del	-/G	9.88777e-05	0.00703058	frameshift-variant	LNX1	GRCh38.p7	4:53476766	ACCGTGGTAATTCCA[-/G]CCACATGACCCAGGA	84708
rs777918909	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53514985	TACCCCATCCAAACA[A/G]CATATTTAATGAATC	84708
rs777972678	snp	G/T	1.65861e-05	0.00287972	missense, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573673	CAACACCTGGGTGCA[G/T]TGCTCCCTGAATGGG	84708
rs778004718	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53613658	CTTTTTCATGGCTGC[A/G]TAGTATTCCATGGCA	84708
rs778012011	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53497902	CAACCTAGAAGGGAT[A/G]GGATAGAACTGTTAT	84708
rs778016390	snp	A/G			intron-variant, upstream-variant-2KB	LNX1, LNX1-AS2	GRCh38.p7	4:53591215	GTTTATTGTGCAACT[A/G]GAATGTCAAAGTCAT	84708
rs778023723	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53585208	TACTGTTTTGTCTTA[C/T]TAGATATCTCACACT	84708
rs778029837	snp	A/G	5.11365e-05	0.00505625	synonymous-codon	LNX1	GRCh38.p7	4:53481831	CTGGCGGGACACGAC[A/G]AGGTGAACACGTCTT	84708
rs778034454	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53614800	TGCTCACATCTGTCT[C/G]CTTCCTTCAGCCTCC	84708
rs778062890	snp	A/T	0.000132968	0.00815268	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498859	CTGAAATGGACAAAG[A/T]GTGTTTATTTAAGAC	84708
rs778063962	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53625591	TGCTTGGGCCCAGGA[A/G]TTTGACACCAAACTG	84708
rs778089443	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53541871	CTTTGTAATAAGTGA[A/C]ATTTGGAGAATTATA	84708
rs778093950	snp	C/T	0.00010051	0.00708835	missense, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573767	AGAACCAGAGGCTTG[C/T]GGTCCATGGGACAGA	84708
rs778105591	snp	C/T			intron-variant, downstream-variant-500B	LNX1, FIP1L1	GRCh38.p7	4:53462923	ACACACTTTACATAA[C/T]GGTTCACTGACTCCT	84708
rs778113420	snp	C/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53505609	TTAATAAGAGGAAGA[C/G]ACTGGTGGAAAGGAA	84708
rs778118854	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53516568	AAATGAGTGACATTG[A/G]TCTAGCAGACTAAGT	84708
rs778128061	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53547839	ACCTCAGAGCTCCCA[C/T]GGAGGGGGATGATGA	84708
rs778136362	in-del	-/AATTTTGCATTATAT			intron-variant	LNX1	GRCh38.p7	4:53620276	ATGTTCACAGGTTAC[-/AATTTTGCATTATAT]AATTTTGCATTATAA	84708
rs778156204	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53572491	TTAGAGAATCCATGC[A/G]TGTCCCAAAAGACAA	84708
rs778181524	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53464296	TGATTAACCTAGCAT[G/T]TATTCCCTCTTCTGG	84708
rs778203126	in-del	-/A			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53593803	CTGAGCACTTTATAC[-/A]AGAACCCTGTGTCAG	84708
rs778211974	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53487238	TTGGCATTGCATGAG[C/T]CCATACAGTGACTAT	84708
rs778213952	snp	A/G	1.66749e-05	0.00288741	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508246	TAACAGAACCAGCGG[A/G]GAGGTGAAGAAGAGC	84708
rs778217749	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53637331	ACCCACTAAATGAAT[C/T]TCTTTGTACCAACCA	84708
rs778223406	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53624608	AATAGTCTCTTTGGT[G/T]CAACTTCATGGCCCT	84708
rs778223575	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53481547	TGCTTGGATGGGAGA[C/T]ACCTGTTATCTCTCC	84708
rs778248243	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53548859	ATAAAAAAGAACAAG[A/T]TCATGTCTTTCACAG	84708
rs778257072	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53564734	TCCATCTGAGGTACC[A/G]GGTTCATCTCACTAG	84708
rs778278178	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53650665	CCGTTCTATACTACC[A/G]CCCTACATATAGGGC	84708
rs778298976	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508740	AGGAGTGAGTTCAGC[A/G]TTGCTATCCTCTAGT	84708
rs778299236	snp	A/G	1.66852e-05	0.0028883	missense, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461460	CATCATTGTATGCTG[A/G]TGTTCCTTCAACAAT	84708
rs778316772	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53626793	GGGTTTCAGAAAAGA[G/T]CTTATAATCATAAAA	84708
rs778344457	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53625626	ACATAGTGACACCCT[C/G]TCTCTACAAAATAAA	84708
rs778346939	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53548810	CTGGGTAATGAAAAT[A/G]TGGTATAGATATACC	84708
rs778401622	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53487717	AGGTGAGAGCTGTAA[C/T]GCGACTGATAACTAT	84708
rs778414806	snp	C/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53595750	TCTGTCTTCAAAGCT[C/G]TTTTCTTGTAGATCC	84708
rs778425246	snp	A/C/T			intron-variant	LNX1	GRCh38.p7	4:53536488	AAGTTTCCTCTTCCT[A/C/T]CCCAACCTTTGTCCT	84708
rs778429792	in-del	-/T			intron-variant	LNX1	GRCh38.p7	4:53611065	AGGTAAAACTGTCTA[-/T]TTTTTGCAAATGATA	84708
rs778438694	snp	C/T	1.65029e-05	0.00287248	missense	LNX1	GRCh38.p7	4:53496303	CGGAACTTCTGTTCA[C/T]GCATCACAGTCAGCC	84708
rs778449962	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53528108	ACACGTGCAGGTTGT[C/T]GCCTAATCCTTTGTG	84708
rs778497657	in-del	-/G			intron-variant	LNX1	GRCh38.p7	4:53566417	TTCAGAAGTGAAGGA[-/G]AAAGAAAATACTTTA	84708
rs778497959	snp	G/T			upstream-variant-2KB	LNX1	GRCh38.p7	4:53653299	TTCCCACTGGTTTGC[G/T]TAAGCACTTCTGTGG	84708
rs778527330	snp	C/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53595886	TTTTTTTTCCCATGA[C/T]ATATTTCTAGAGTTG	84708
rs778532000	snp	A/G			intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53559684	TGGGGGTCTTGCTCT[A/G]TCACCCAGGCTGTAG	84708
rs778541775	snp	A/G	1.65433e-05	0.002876	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508124	CTGCAGAAACCTCTG[A/G]GGAGGGAGCCGTGGC	84708
rs778543079	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53638067	TAGTTTCAGAGGGAA[A/G]TATGAATGACCACTT	84708
rs778545185	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53489946	GGCAATTCTTACTGG[C/T]TCCGGGGGACTTGAA	84708
rs778576262	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53464580	TATGAGAGAAATGCC[G/T]AGTCCCCATATTAAA	84708
rs778584257	snp	C/T	9.88484e-05	0.00702954	missense	LNX1	GRCh38.p7	4:53496255	TCATCTCGGGGTCTG[C/T]AGGCATCCGGGGCCT	84708
rs778613654	in-del	-/CA			intron-variant	LNX1	GRCh38.p7	4:53533552	ACAGGCACATGCCAT[-/CA]CACACCTGGCTAATT	84708
rs778619926	in-del	-/C	1.64727e-05	0.00286986	frameshift-variant	LNX1	GRCh38.p7	4:53496157	CATTGAAGATGAAAA[-/C]CCCAGGCTCATCCAC	84708
rs778621360	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53464108	GATGTTTTGAGCTCT[G/T]TGAGAGCAGAAAATT	84708
rs778649089	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53617082	AAAGTTATAAAACAT[A/G]TAAACTATAATACAA	84708
rs778654374	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53528725	AACTAGTGAGAACAG[A/G]TAATTGACCAAAGCT	84708
rs778660518	in-del	-/G			intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53574333	TCCTCACATTGGTGT[-/G]GTAAGAATCATTTGG	84708
rs778660537	snp	C/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53600004	GATGAATTTAAAATT[C/T]CTTTAAGGTAGAGTT	84708
rs778664371	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53480466	ACTAAAATTAGTTAA[C/T]TGGATAAAAACTTCA	84708
rs778666229	snp	G/T	1.65386e-05	0.00287559	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508223	AGTGGGAGGCACCTT[G/T]ACAGCTGTAACAGAA	84708
rs778682497	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53520202	GCCTCTCACAGCAAC[C/T]CCTGCGGGTCCAAAC	84708
rs778704506	snp	G/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53600209	TGTCCAATAGAGTAC[G/T]CTGTCCTCTAAGAGC	84708
rs778709883	in-del	-/G	3.46891e-05	0.00416453			GRCh38.p7	4:53558016	TTCTGTCAGCTACAA[-/G]GGCCCAAACCAGCCA	84708
rs778759914	snp	C/T					GRCh38.p7	4:53618762	AGTTCATTTTAATAC[C/T]GTATTTTAGCTAACT	84708
rs778766608	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53532142	AGGGATGGACCAAGG[A/G]CACAAATACTATCAC	84708
rs778788782	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53589509	TTCCAAAGGAAGAAC[C/T]TAGCCTCAGTTTAGC	84708
rs778792677	snp	A/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53502724	AGTAGAACTTCTTTC[A/T]AAATTAGAGTCAATC	84708
rs778796565	snp	C/G	1.64969e-05	0.00287196	missense	LNX1	GRCh38.p7	4:53478585	TTTATTCTTCCATCT[C/G]TGCTTATGACTCCTC	84708
rs778810117	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53531348	ACTTCATTCTCTTAA[C/G]TAAATCACTTTATTT	84708
rs778810129	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53556016	TAGTCAGTGGAGTGG[G/T]GGCCCCCAAAAGATG	84708
rs778857937	snp	C/T	1.71469e-05	0.002928	missense, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573900	TGAGGTCATCATCCA[C/T]TTCCTCTGGATAGCT	84708
rs778887979	snp	C/T	4.95692e-05	0.00497816	intron-variant	LNX1	GRCh38.p7	4:53476721	AATCGTTTTCTCCCA[C/T]GCCCCTACAGGGATG	84708
rs778891452	snp	C/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53598001	AATCCCATGAACTAA[C/T]TACAAACAGGTGAAG	84708
rs778906297	in-del	-/C			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53523656	CCTATTAGTAGGAGA[-/C]TAGGAGACTAGGGAT	84708
rs778906365	in-del	-/AAAA			utr-variant-3-prime, downstream-variant-500B	LNX1, FIP1L1	GRCh38.p7	4:53460285	TACTAAAAACAAAAC[-/AAAA]AAGTTTATAATTAAT	84708
rs778911332	snp	C/G/T	6.59048e-05	0.00574009	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507383	TGGCAACTGCACTCC[C/G/T]GCTCTTTGTCCTTCG	84708
rs778918450	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53546471	ACTAGCTCCAATTTT[A/T]TTGCTTCCTCAGGAC	84708
rs778918501	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53533478	TTCTCAGCTCACCGC[A/G]ACTTTTGCCTCCCAG	84708
rs778949770	snp	A/G	3.85498e-05	0.00439015	intron-variant, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573585	CCAGCTGTCCCGCTT[A/G]GGGGTGGGACTTACC	84708
rs778981190	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53552635	GGAGTTCGAGACCAG[A/C]CTGACCAATATGGTG	84708
rs778988966	snp	A/C	1.71628e-05	0.00292935	intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461609	CTGAAATAGAATGTA[A/C]TCAGTGTACATGCAT	84708
rs778990592	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53557218	GAGATGCACAATGAT[A/G]TATTTAGGGGTGATA	84708
rs778994289	snp	C/G			utr-variant-5-prime, upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53591462	TGTGGGTGAACCGAG[C/G]AGCTCCTTGGGCCGC	84708
rs779001826	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53541951	GGCAAACATGAGCAT[A/G]CATAAATCAGCTGCT	84708
rs779045890	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53505983	AGCATGCAGCATGTA[C/T]GTGCAGGGTGAGAGG	84708
rs779048775	in-del	-/ACA			intron-variant	LNX1	GRCh38.p7	4:53529121	CACACACACACACAC[-/ACA]CACACACACACAAAC	84708
rs779066897	in-del	-/AAGTGACGTCTC			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53514458	AGATGAGGAGGAGCA[-/AAGTGACGTCTC]ATATGGCGGCAGGCA	84708
rs779096642	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53560425	AACCACTGCTGGTTG[C/T]CTATCAAATATTTAA	84708
rs779199927	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53623141	CATTGCACGGCTGGA[A/C]TATATGTGGGCTAAC	84708
rs779231642	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53488565	TTGTTGATGAACCAG[A/C]TGCACTGAGGACCTC	84708
rs779237078	snp	A/G			upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53592583	GCCTGCCTGCCCAGA[A/G]AGAATTTTTTTTCCC	84708
rs779247649	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507309	AGCCTTATGGGGAGT[C/T]CATTTACCTTCAGGG	84708
rs779247858	snp	C/G			intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53499136	AGCTATTTCTCATGG[C/G]ACTCAACCCATTATT	84708
rs779263083	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53538707	TTGAAAGAGCCTTCA[A/G]ACTCACAGGTGTTCA	84708
rs779263911	snp	A/T	2.59535e-05	0.00360223	missense, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573662	TCACAGCGCTGCAAC[A/T]CCTGGGTGCAGTGCT	84708
rs779266905	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53525512	AAAGATGCTTGGTTT[C/T]CTGCCTGGAATTCCA	84708
rs779283487	in-del	-/ATCT			utr-variant-3-prime, downstream-variant-500B	LNX1, FIP1L1	GRCh38.p7	4:53460421	GATAATACAAAAGTA[-/ATCT]ATCTTAATTAGTATC	84708
rs779308093	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53632535	TTTGCCTCATGGCAG[C/G]ATGAATTCTGGGGTG	84708
rs779319489	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53502236	CAAGTCACATGGATT[A/G]CACTGTCCCCTATGG	84708
rs779321502	in-del	-/GAAG			intron-variant	LNX1	GRCh38.p7	4:53477229	CACAAGAATACCGCT[-/GAAG]GAAGGAAGGAAGGGA	84708
rs779324656	snp	C/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53516528	AGGCTTCTTAGAAGA[C/G]ATGAAATCTGAGCTG	84708
rs779369279	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53626880	ACCCATCTGTGCCAA[A/C]AGTCTGAAATGGAAA	84708
rs779384285	snp	C/G			upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53593242	GTCCCCTGGGCAAGG[C/G]GGAGGGGAGGGAGAG	84708
rs779429022	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53570819	GATCACGAGGTCAGG[A/T]GATCGAGACCATCCT	84708
rs779440555	in-del	-/GGCCCT			intron-variant	LNX1	GRCh38.p7	4:53613984	CTGTTATTTTTTGAC[-/GGCCCT]GGCCCTTTTTTGATA	84708
rs779451325	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53586505	CACAAGAAGCAAATA[A/G]GAGTCACTTGAAAAA	84708
rs779451671	snp	C/T	1.66449e-05	0.00288482	missense	LNX1	GRCh38.p7	4:53481764	CTGGGGACCAGCTGC[C/T]ATTGCTGTTCCAGCC	84708
rs779451915	snp	C/T	1.65217e-05	0.00287412	stop-lost, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460908	ACCCATCATTGATTC[C/T]ATAAAAAAGTGCCAG	84708
rs779457356	snp	C/T			intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53499244	TCTCACTACAACCTC[C/T]GCCTCCTGAGCTCAA	84708
rs779474385	in-del	-/A	0.086814	0.189457	splice-acceptor-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461044	AATATCACCACATCT[-/A]AAAAAAAAAAACAAA	84708
rs779478850	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53631423	ATCTAGTTCCACTTT[A/G]CATTTGATAGGAAAT	84708
rs779495889	snp	C/T			synonymous-codon, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573715	TAGCTTGTTGAGGAG[C/T]TTGTTGACCAGGATG	84708
rs779544704	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53538234	TTGGGACACCATGGC[A/G]TCCAGGTTTTATCTG	84708
rs779553215	snp	A/G	1.67144e-05	0.00289084	intron-variant	LNX1	GRCh38.p7	4:53478772	GGAAAAACATGGCAC[A/G]TGAATTCACAACTCT	84708
rs779570581	snp	A/G			upstream-variant-2KB	LNX1	GRCh38.p7	4:53653043	ACCATCATCATCATC[A/G]TCAGTGGCTGCAGCA	84708
rs779576535	snp	C/T			utr-variant-5-prime, upstream-variant-2KB	LNX1	GRCh38.p7	4:53652463	ATGCATTAGCATCAG[C/T]GACAAATCTCTTCTG	84708
rs779577868	snp	C/G	1.65573e-05	0.00287721	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508106	TTAAGGAGATGGTGG[C/G]AGCTGCAGAAACCTC	84708
rs779611720	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53586460	TGCTGCTGGTGAAGT[A/C]TTTTGTGTGCCTGTG	84708
rs779634161	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53526920	AAAATTATAGAGCTA[A/G]TTCTTCTTTGTAAGA	84708
rs779641005	snp	C/T	1.65345e-05	0.00287524	utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460896	TGTTTTCCTCTGACC[C/T]ATCATTGATTCTATA	84708
rs779689304	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53550373	GTAAACTCTACCTCC[C/T]TCCTTCCAGGTCCTC	84708
rs779706674	snp	C/G	0.000102904	0.00717225	synonymous-codon, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508035	GCTGATTGCTGGCTG[C/G]CCGTCCTCTGCCGAG	84708
rs779709623	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53492788	CTAGGGGAGAGCACG[C/T]TGGGCAAGGGGTGGA	84708
rs779717306	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53483311	TGTGAGTTCATTAAA[C/T]CTTTATAAATGACCC	84708
rs779741715	snp	A/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53596821	TTCCCCTCTACTTCT[A/G]TTGAGTCACCCATTC	84708
rs779747748	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53561913	CCTGAACGTTCTGTA[C/T]GTGTATCCCAGAATT	84708
rs779765145	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53552522	TAAGTTTTTTTCTTG[C/G]ATTTTTGTTAAACTT	84708
rs779771376	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53620330	ATATTATAAATGCAA[A/C]CTCTCAAGCCCTGAC	84708
rs779773711	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53485964	GACAGCTTCTCTCTT[G/T]CATCTCTTGGGATGT	84708
rs779773753	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53627632	TAATTTTTAAATAAA[G/T]GCACAGAGGTGAGTA	84708
rs779796246	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53618675	TGCTGGCCAATAGGA[C/T]GACAATGCAAGCCAC	84708
rs779822876	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53521347	TTCCCAGACATTTGA[A/G]AACATTTCCTCCGTT	84708
rs779826454	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53608408	CAAATCAAAGCCACA[A/G]TGTGATACCATCTCA	84708
rs779828164	in-del	-/GAAAT			intron-variant	LNX1	GRCh38.p7	4:53469254	TACTAGGTACATAAC[-/GAAAT]GAAGGCAGAAATAAA	84708
rs779839797	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53528856	CATCCATAGCCAAAG[A/G]TATTGGCTCTGGGAT	84708
rs779840059	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53555183	GAAGGCCTCCATCTC[A/G]GACATGCAGGCATCA	84708
rs779857047	snp	G/T	1.64738e-05	0.00286995	missense	LNX1	GRCh38.p7	4:53476828	TGGTTGGAGTCCAGG[G/T]CTGCTGGGCTGCTGC	84708
rs779874766	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53493034	GAGTGCAGTGGTGCG[A/G]TCTTGGCTCACTGAA	84708
rs779903330	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53579696	GTGGAAACATTTCTG[C/T]ATCAGGTAACTCATC	84708
rs779912662	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53522109	CTGCTCAGTTCTTTT[C/T]GTTTGGCAGACGAGG	84708
rs779913117	snp	A/C/T			intron-variant	LNX1	GRCh38.p7	4:53493537	CTTGGTCCTCTTCCA[A/C/T]GAAGAGGGATAAGCT	84708
rs779921708	in-del	-/ATTT			intron-variant	LNX1	GRCh38.p7	4:53644556	AGTCCATGATAAGAA[-/ATTT]ATTTACACAATGAAG	84708
rs779923788	in-del	-/TCT	1.76263e-05	0.00296864	cds-indel, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573989	GGATCGTTGGCAGAC[-/TCT]GGCTGGTTCATGATG	84708
rs779938177	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53536578	TACCAGCTCTGGACC[A/G]GATCTCAGGGCCTCT	84708
rs779945559	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53532230	CCTATAATCCCAGCA[C/T]TTGGGGGTGCTGAGG	84708
rs779946904	in-del	-/C	1.75699e-05	0.00296389	frameshift-variant	LNX1	GRCh38.p7	4:53496381	GGACATTGCTGATGT[-/C]CCATCCCGTTGACCT	84708
rs779966625	in-del	-/GCCGT			intron-variant	LNX1	GRCh38.p7	4:53633862	CATAACCTTCTTAGG[-/GCCGT]GTTTCTGCATCACCA	84708
rs779974005	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53639584	ATGGTGCAAACAAAG[A/G]CTCACAGGAACCCAA	84708
rs780013391	in-del	-/CTGTTATGA			intron-variant	LNX1	GRCh38.p7	4:53495072	GGTGATGGAAATCTT[-/CTGTTATGA]CTGTTAATGTCAATA	84708
rs780013713	in-del	-/AG			intron-variant	LNX1	GRCh38.p7	4:53606206	TAATAAAGAAAAAAA[-/AG]GGGAGAAGTTCCAAA	84708
rs780018488	snp	C/T	6.59152e-05	0.00574049	missense	LNX1	GRCh38.p7	4:53476928	ATAATGCCACTGCCT[C/T]ACTCCGGCTGACCTC	84708
rs780027477	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53616823	TCTCCCAAGATAACA[C/T]AGGTAAATGGCAGAG	84708
rs780039672	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53637558	AAGTTGTAGCATTGC[G/T]CAATCCCCACGACAC	84708
rs780049322	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53524171	TTAAATTATATATAT[A/T]TTTTTTCTCTTCTAA	84708
rs780052635	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53480261	GGAAATAATTACAAT[A/T]CCGACTAAGTCAGTT	84708
rs780104294	snp	A/G	1.96825e-05	0.00313702	missense, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573773	AGAGGCTTGCGGTCC[A/G]TGGGACAGAAGTCCT	84708
rs780117310	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53546808	GCTAAATAGCTGAGG[A/G]ATGAAGGCTGGGGAG	84708
rs780138825	snp	A/C/T			intron-variant	LNX1	GRCh38.p7	4:53525454	TACTTCACTGCAGAG[A/C/T]GGGTGACAGCATTCT	84708
rs780142926	snp	C/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53600772	GTCTCGCTCTGTTGC[C/T]AAGGCTGGAGTGCAG	84708
rs780163944	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53563415	CTCCAGAGGTATTAA[C/T]TACTTCTTAAGTATT	84708
rs780190293	snp	C/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53599251	CAGGTCAGAAAGACT[C/T]TGCTGATAAAACAGG	84708
rs780207321	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53531136	ACACACAGACACACT[G/T]CTTTAGTCTCATACT	84708
rs780216241	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53644479	GTGACTTAAGCTAGA[A/C]TGATGTATTATATAT	84708
rs780227760	snp	G/T	1.74045e-05	0.0029499	synonymous-codon	LNX1	GRCh38.p7	4:53481852	AACACGTCTTTCACT[G/T]GCCTGGGCAAGAAGA	84708
rs780249985	snp	A/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53594415	TTAATCCGAGTGGCC[A/G]TAAGAACATGGAACT	84708
rs780289369	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53612558	TAAGAATAAATTAAC[G/T]CTTGTAATCCCAGCA	84708
rs780301333	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53582907	AACAGACCAGCGCCT[A/G]CCACTTCTTCAAATG	84708
rs780305255	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53536747	GTTCTTGACAAACCA[C/T]TCCTTTGTTTTTCTA	84708
rs780316057	snp	C/T	3.36383e-05	0.00410098	synonymous-codon	LNX1	GRCh38.p7	4:53496038	CTGAATCAGATGAGC[C/T]GCACTTTCTGGGCTG	84708
rs780354148	snp	C/T			nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53604541	TTATAATGAGGGCTC[C/T]GAATTCTTATGGGTT	84708
rs780365708	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53630835	ATTTGCTAATTCAGT[A/G]TTTGCAGTGATTTTA	84708
rs780378304	in-del	-/C			intron-variant	LNX1	GRCh38.p7	4:53590833	AAAGAAAATGGTAGA[-/C]TTTTTCAGAGAAGAG	84708
rs780389476	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53623286	TTGGCTCACTGCAAC[C/T]TCCTCCTCCCAGGCT	84708
rs780390920	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53476656	GGTCTAATTAAGATG[C/T]TAGTGCCATGAATCA	84708
rs780395944	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53528198	TCAATCATTGGGGGT[C/T]ATCCAGAGATGACAG	84708
rs780398664	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53632902	CTTTCTTACTCCCCT[A/C]CTCCTGATTACACTT	84708
rs780407653	snp	A/C			upstream-variant-2KB, intron-variant	LNX1, LNX1-AS2	GRCh38.p7	4:53592881	AAGAGAAATTGTAGT[A/C]GAGGGCGGGGTCTGG	84708
rs780409322	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53478170	CAAATCTATCAAATG[A/C]CTTTTTCTATCTAAC	84708
rs780468999	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53557172	GCATAAAATGGACAT[A/G]TGTCATGTAGGAAAT	84708
rs780473333	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507139	TATGTAAAAAGATGA[C/T]AATACTTTCTGCCTT	84708
rs780475559	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53495113	ATGCTTGTGATGCCA[C/T]ACTATGGTTTTGCAA	84708
rs780495550	snp	C/T	1.68272e-05	0.00290057	intron-variant, upstream-variant-2KB	LNX1, LNX1-AS1	GRCh38.p7	4:53498612	TTATATCAAGCCCCT[C/T]GCTGCAGCCCCACAG	84708
rs780496017	snp	C/T	1.65326e-05	0.00287507	intron-variant	LNX1	GRCh38.p7	4:53476711	TAAGAAATGTAATCG[C/T]TTTCTCCCACGCCCC	84708
rs780509537	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53539948	GGCAAAGGTTGACTT[G/T]GCCATGTGGTTAGAA	84708
rs780510156	in-del	-/CT			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53514262	GGCATATAGAAGGTG[-/CT]CTCAGTGTATGACTT	84708
rs780519862	snp	A/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53603474	CGTTCTTGCATTGGT[A/G]TAAGGAAATATCTGT	84708
rs780523932	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53545676	TTTAATTCTTACCCC[C/T]ATGAGGTAGGTGCCA	84708
rs780549902	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53608932	GTGTACACAAAGAAG[A/G]GAACAACAGACATCA	84708
rs780581305	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53489364	GCATGTATCTTTAGA[G/T]GCAAAGACATTAATG	84708
rs780593476	in-del	-/CGAGGTCAGGAGAT			intron-variant	LNX1	GRCh38.p7	4:53570809	GAGGCGGGCGGATCA[-/CGAGGTCAGGAGAT]CGAGACCATCCTGGC	84708
rs780598247	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53506154	CTCTGGAACCAGAGG[A/G]CCTGATTTAAAATCT	84708
rs780651533	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53615010	GAATGAGAATAAAAT[A/T]TATTTTTCCTTTTCC	84708
rs780671466	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53463875	AGTCAATACATATTT[A/G]AGAACACTGACTTTG	84708
rs780676880	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53529200	CTTAGGCACTGAACT[A/G]ACACAATCTAGGAGA	84708
rs780688989	in-del	-/A	1.8812e-05	0.00306686	utr-variant-5-prime, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53574039	ACAGGAAACTCAGTC[-/A]CACAATATTTCCTCA	84708
rs780750163	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53489392	ATGATAATACAGATG[A/G]TGACTTATATGGGGT	84708
rs780755378	in-del	-/T			intron-variant	LNX1	GRCh38.p7	4:53556648	TGCTCATGATTCAGA[-/T]TTAAGCTAGACACTT	84708
rs780772808	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53649243	CCCTTTTTGATCCAC[C/G]TACTGGAAAATAACA	84708
rs780785707	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53472322	AAGGGGAACATCACA[C/T]ACCGGGGACTGTTGT	84708
rs780786679	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53638422	GTAACCCCAAACTCA[A/G]TGCTCATGGTGCTTT	84708
rs780790235	snp	C/T	1.64773e-05	0.00287026	missense	LNX1	GRCh38.p7	4:53478612	CCTCCGGGCTCAACA[C/T]TGATGACATAGATAG	84708
rs780798268	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53616499	CACAGAATGAATGGT[C/T]TGATTCATTTGGCCT	84708
rs780816206	snp	A/C			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53598827	TTCACAATAATTCAC[A/C]ATAATGAAGACATTA	84708
rs780826379	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53540267	GTGCACCTGTAGTCC[C/T]AGCCACTCGGGGGGC	84708
rs780851611	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53617603	AAATATTTTTATACA[A/G]CCTTGTTGGTGAAGA	84708
rs780862429	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53465909	CTAACTTAAAATGCT[A/G]CTTTATTATAGGAAG	84708
rs780881155	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53551413	TGAAACTGGTGATCA[C/G]CTTCCTAGTAAGATC	84708
rs780886650	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53550601	GTGAAAATGAAGTGG[C/G]GAGGAAATGGATGCT	84708
rs780911574	snp	C/T			upstream-variant-2KB	LNX1	GRCh38.p7	4:53652696	TCATTAGGTCTGGAA[C/T]ATTATCATGCTGGGA	84708
rs780944987	snp	A/C/T	5.05109e-05	0.00502527	missense, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508015	CTCCGGCCAGAGTCC[A/C/T]CTGGGCTGATTGCTG	84708
rs780951327	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53494850	AGCTTATGAAACGTC[A/G]CTGAGACACAAAACT	84708
rs780973325	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53648689	GGGGAAGGAGAACTG[A/C]CTCACAGCTCCAACA	84708
rs780990741	in-del	-/A			intron-variant	LNX1	GRCh38.p7	4:53466161	TTTGTTTTAAGAAAA[-/A]AAAAATCACATATTA	84708
rs781049023	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53471892	ACACTGTTGGTGGGA[C/G]TGTAAACTAGTTCAA	84708
rs781079167	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53563131	GAATGGCATGAATCC[C/T]GGAGGCAGAGCTTGC	84708
rs781081990	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53544983	AGACCTATGTAGAGT[C/T]TGCATTGCACGAAGG	84708
rs781084127	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53608589	AGCAGGATTACCATT[A/C]GACCCAACAATCCCA	84708
rs781109488	snp	C/T	3.43065e-05	0.00414151	missense, upstream-variant-2KB	LNX1, LOC101928879	GRCh38.p7	4:53573893	TGGCAGATGAGGTCA[C/T]CATCCACTTCCTCTG	84708
rs781129686	snp	G/T	1.67371e-05	0.0028928	utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460857	ATATAGTGTTTCAAC[G/T]TCTTAGCCTATTTGT	84708
rs781162800	in-del	-/AC			intron-variant	LNX1	GRCh38.p7	4:53636583	TTGTGGTGTGTCAAA[-/AC]AGTTATACAAAATGA	84708
rs781163761	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53532454	TCAAATAAATAAATA[A/G]ATAAATATATGAATA	84708
rs781166753	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53510996	TGCACTTTCAAATTC[C/T]TGGGGTTCTAAAGAT	84708
rs781189758	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53642514	CACCAGCTAGGGGCC[C/T]TTCCCACATACCCTG	84708
rs781223377	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53642087	ATCAGCCAGGTTTGG[C/T]GGTACACGCCTGTGA	84708
rs781240190	snp	A/G			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53598234	TATTTTACTGACTGT[A/G]ATTTTTTTTTTTTTT	84708
rs781246892	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53612682	AAAAATCAGCTGGGT[A/G]TGGTATGCCAGCTAA	84708
rs781247325	snp	A/G	1.65015e-05	0.00287237	intron-variant	LNX1	GRCh38.p7	4:53476732	CCCACGCCCCTACAG[A/G]GATGTTGTGTTTGGA	84708
rs781248956	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53536357	GGACTTTTACACAAA[C/T]GCCACACACAGTCAA	84708
rs781275160	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53580776	ACTCATAATGTATAT[A/C]CAATCCTTAGAACCA	84708
rs781276366	in-del	-/C			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53515475	GCAAGCTCATGAGTT[-/C]CCCTTTCCATTTCCC	84708
rs781282574	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53502052	ATCTGACCTTCACCT[C/T]ATCTTCTGTATTGGT	84708
rs781284731	snp	A/C			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53514711	TTGGCTATCTACACT[A/C]ATCAGATGACTCAGG	84708
rs781295462	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53554117	GACTGTTAGGGAGAG[A/G]GTCCTAAGCAAATAT	84708
rs781331599	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53581534	ACTCACAGTTCCATA[C/T]GACTGAGGAAGCCTC	84708
rs781387422	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53630199	GGACTTTCAAATTAA[C/T]AGCAAGTCATTAAAA	84708
rs781394484	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53628714	ACAATTGCAGAGATA[C/T]GGAACCAACCTAAGT	84708
rs781397480	snp	G/T	1.67365e-05	0.00289275	intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507275	GAAGTCCCCCTGGAA[G/T]CCCAGCCCATGTCCA	84708
rs781434160	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53589008	GGGCTTCCTCCTGCC[A/G]GAGGCTCGGCATGAA	84708
rs781435456	snp	G/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53508499	TGGAATGCAAATTTA[G/T]TCAGGTCACCATGGT	84708
rs781480202	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53635385	TTAGGGTTGTCTCAC[A/G]TAACTCACTACAAAG	84708
rs781502995	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53478310	AACTTGCTCATAACT[A/G]TAGCAGTTCTCTATT	84708
rs781506030	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53519725	CGTCAGGCTATTCTG[A/G]GCACTCTACCCTTTA	84708
rs781506622	snp	C/T			intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461770	CTGTTAGCTGGCTTT[C/T]TGTAATTGAACCTGT	84708
rs781521382	snp	A/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53517037	TATAGATAGCTTCCA[A/T]GGGAGTAAACGTCCT	84708
rs781522036	snp	A/G	3.29495e-05	0.00405877	synonymous-codon, intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53507363	CCTGCCCTGGTCGGC[A/G]TGGTTGGCAACTGCA	84708
rs781553139	snp	C/T	1.66457e-05	0.00288489	missense, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461475	GTGTTCCTTCAACAA[C/T]GGATTTGATGAAAAA	84708
rs781566736	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53587558	ATACTGAGGCAATGA[A/G]GAGGACACACTTTAG	84708
rs781579629	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53535290	GATGCTTAAGCCATG[A/C]CTCTTTTAGTCCTTT	84708
rs781629610	snp	C/G/T	4.94575e-05	0.00497259	intron-variant, missense	LNX1	GRCh38.p7	4:53557944	TGAGCCAAGGCAAGA[C/G/T]CAGCAACAGAAGCGC	84708
rs781631874	in-del	-/TGTT	6.62109e-05	0.00575335	utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53460880	TATTTGTGATTTTTC[-/TGTT]TGTTTTCCTCTGACC	84708
rs781632659	in-del	-/TA			intron-variant	LNX1	GRCh38.p7	4:53565222	ACAAAAAGACAGCAG[-/TA]ACCTCTGCAGACTTA	84708
rs781659224	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53542219	TAGGAAAGTAAAATT[G/T]AGTTTCCAGAAAACC	84708
rs781665612	snp	C/T	3.39271e-05	0.00411854	intron-variant, utr-variant-5-prime	LNX1	GRCh38.p7	4:53558002	TCTCCCTGGCCACCT[C/T]CTGTCAGCTACAAGG	84708
rs781688085	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53645437	CATTGGGGTTACCCA[A/G]TGGGGTCTATTCCAG	84708
rs781753746	snp	A/G			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53518812	GGCAACTGTAACATG[A/G]GACGTAGGGAAAAGC	84708
rs781766960	snp	A/C			intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53559273	TAATTTCTACAGTTT[A/C]AAGTGCAGATGAACA	84708
rs796067642	in-del	-/A			intron-variant	LNX1	GRCh38.p7	4:53543537	AAAGAAGAAAAAAAA[-/A]TCACACTATACAAAG	84708
rs796088095	in-del	-/TT			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53501282	TAGATGATAATAATC[-/TT]TTTTTTTTTTTTTTT	84708
rs796101323	multinucleotide-polymorphism	CTC/TTT			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53596709	TTAAAATGTCTCTTC[CTC/TTT]TTGTTAACTTTGACT	84708
rs796112949	in-del	AAAA/C			intron-variant	LNX1	GRCh38.p7	4:53472688	AACAACAACAACAAA[AAAA/C]AAAAAAACAAAAAAC	84708
rs796114674	in-del	-/ATAT			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53594153	ATAATATATATATAT[-/ATAT]GTATATATAAATATG	84708
rs796119095	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53466380	CTGAAGACAGCCGAA[G/T]AGGAACAGCTCCAGT	84708
rs796148090	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53485406	ACATCGAATCAACTT[G/T]CCAGGCAAAATCCAA	84708
rs796165854	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53490027	AAATAGTCCATTATT[C/G]GCTTTGTGGCTCTGT	84708
rs796193604	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53550112	GGATCACAATGCTCT[C/T]TGGACATCAAAGAAT	84708
rs796196456	snp	A/G			intron-variant, upstream-variant-2KB	LNX1	GRCh38.p7	4:53558663	TCAGAATAACAAAGA[A/G]CCTGGATAGACATAA	84708
rs796209130	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53487296	GTAAGAACTGGTCAA[A/G]TACCTGTTCTCATCC	84708
rs796220106	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53585258	TAGGCCTTTAGAGTA[C/T]AAAACACTTACTACT	84708
rs796248136	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53484521	CGAACCGAGATTGTG[A/G]CACTGCACTCAAGCC	84708
rs796254534	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53636449	GGTGAGACATTCTTG[C/T]CCCTCAGAGTAGAAA	84708
rs796265459	in-del	-/G			intron-variant	LNX1	GRCh38.p7	4:53528685	CCTGTGGATAAGGGG[-/G]GGACTACTGTATAGC	84708
rs796292157	snp	A/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53595850	ATTCAGCAGAATTAC[A/T]TTGCCCATTTTGCTT	84708
rs796294846	snp	G/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53512234	GGAGAAATTTGGAAG[G/T]TTTTCAATGTAAAAT	84708
rs796318218	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53649538	ATCTCCACAGCCTGC[A/T]CCTGTCTGGACAGCT	84708
rs796372199	in-del	-/T			intron-variant	LNX1	GRCh38.p7	4:53634253	TCTGTCCAGCTTGGC[-/T]TTTTTTTTTTTTGAG	84708
rs796395112	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53501729	GAAGCTAACTGTAGG[C/T]TGCTGAAGCAATGAG	84708
rs796404106	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53466713	CCTGGCTCGGAGGGT[C/T]CTATGCCCAAGGAGC	84708
rs796404850	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53652039	AGAGAGAGAGAGAGA[G/T]AGAGAGAGAGAGAGA	84708
rs796428621	in-del	-/CA			intron-variant	LNX1	GRCh38.p7	4:53554851	AGCGAGACTCTGTCT[-/CA]AAAAAAAAAAAAAAA	84708
rs796430309	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53581387	AGTTTTGTTTTCCTG[A/G]CTTTAAAGGAAACAC	84708
rs796455244	in-del	-/AA			intron-variant	LNX1	GRCh38.p7	4:53491286	GAGAAAAAAAAAAAA[-/AA]TCTTGCTAAGAATGC	84708
rs796471057	snp	A/T			intron-variant	LNX1	GRCh38.p7	4:53618840	TATTTATGTCCCTTT[A/T]AAAAAAAATTTGGTC	84708
rs796497095	in-del	AGGGA/G/GG			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53601100	GAAAGAAAGGGAGGG[AGGGA/G/GG]GGGGGGGAGGGAAGG	84708
rs796527288	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53623183	TGTACCTGAGGATGA[C/G]AGCGTTTGCGTTGAG	84708
rs796534483	snp	C/G			intron-variant	LNX1	GRCh38.p7	4:53628326	CCATCAAAAAGTAGG[C/G]AAATGGCATGAATAG	84708
rs796544175	in-del	-/C			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53595849	GATTCAGCAGAATTA[-/C]TTTGCCCATTTTGCT	84708
rs796610435	in-del	-/A			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53515512	CAATTTAAGGCCCCC[-/A]ACCCCACCAAAAAAA	84708
rs796626784	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53636445	CTCTGGTGAGACATT[C/T]TTGTCCCTCAGAGTA	84708
rs796628652	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53518119	GAAAATGCAGGCCAC[C/T]ATCATGGGCACCTGG	84708
rs796644080	in-del	-/A			intron-variant	LNX1	GRCh38.p7	4:53609286	AAAAGTAAAAAAAAA[-/A]GGAAATCTAAAGAGA	84708
rs796667980	in-del	-/T			intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53605641	TTCTCTGTATTCATG[-/T]TTTTTTTTAAAATTC	84708
rs796672924	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53466393	AATAGGAACAGCTCC[A/C]GTCTACAGCTCCCAG	84708
rs796680224	multinucleotide-polymorphism	AG/GA			intron-variant	LNX1	GRCh38.p7	4:53541147	ACTCAAAAAAAAAAG[AG/GA]AAAAAAAAAAGAAAG	84708
rs796701917	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53634463	TGGCCAGGCTGGTCT[C/T]GAACTCCTGAGCTCA	84708
rs796706788	snp	C/T			nc-transcript-variant, intron-variant	LNX1-AS2, LNX1	GRCh38.p7	4:53603687	TTAAACCACGTCTTG[C/T]AAGAACTCACTATTG	84708
rs796715266	in-del	-/A			intron-variant	LNX1	GRCh38.p7	4:53539389	TTAATTTTTGAGACC[-/A]TGTCTCACTCTGTCG	84708
rs796720481	in-del	-/C			intron-variant	LNX1	GRCh38.p7	4:53486305	AGCGCACTACAGCCC[-/C]AGAGCTCCTGAGCTC	84708
rs796756888	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53620514	TCAGACACAGTGTTA[G/T]GTGTTGGGTGCATTC	84708
rs796774163	in-del	-/AA			intron-variant	LNX1	GRCh38.p7	4:53610732	AAAAAAAAAAAAAAA[-/AA]GAAATAAACCAAATC	84708
rs796782959	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53584004	GAGTATTTTTGCATT[A/G]ATTCGGAGCTCTGTT	84708
rs796791812	snp	C/T			intron-variant, nc-transcript-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53523043	AAGATTTTTAAAAAT[C/T]TAGCTTATGAGATAC	84708
rs796807286	snp	A/G			intron-variant	LNX1	GRCh38.p7	4:53469166	CAGTGCAATCAAACT[A/G]GAACTCAGGATTAAG	84708
rs796811165	in-del	-/A			intron-variant	LNX1	GRCh38.p7	4:53549173	ATCTAAAATAAAAGT[-/A]AAAAAAAATAAGTTC	84708
rs796818498	in-del	-/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53502949	CTTTTTTTTTTTTTT[-/T]AGATGGAATCTTGCT	84708
rs796835798	in-del	-/A			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53512386	TGGTAATTAAAAAAA[-/A]CTGCCAACACAAGTA	84708
rs796840737	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53585513	GACCTTACAGGAAAA[C/T]GATCTAAGAAGGTGT	84708
rs796846473	snp	A/C			intron-variant	LNX1	GRCh38.p7	4:53571675	CAAATTTGTTTTTTT[A/C]TTTTTTTGAGACAGT	84708
rs796917462	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53562290	GTAATGGCCTCCAGT[C/T]AGGAAGGCTGCCATT	84708
rs796929355	in-del	-/AA			intron-variant, utr-variant-3-prime	LNX1, FIP1L1	GRCh38.p7	4:53461045	AATATCACCACATCT[-/AA]AAAAAAAAACAAAAC	84708
rs796974008	in-del	-/CT			intron-variant	LNX1	GRCh38.p7	4:53539389	TTTAATTTTTGAGAC[-/CT]GTCTCACTCTGTCGC	84708
rs796975032	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53534559	AGGTGGGAGGATCAC[C/T]TAAACCCAGGAGTTT	84708
rs797003655	snp	C/T			intron-variant	LNX1, LNX1-AS1	GRCh38.p7	4:53518815	AACTGTAACATGGGA[C/T]GTAGGGAAAAGCATG	84708
rs797018379	snp	G/T			intron-variant	LNX1	GRCh38.p7	4:53652041	AGAGAGAGAGAGAGA[G/T]AGAGAGAGAGAGAGA	84708
rs797020483	snp	C/T			intron-variant	LNX1	GRCh38.p7	4:53643213	TGGAGTGCAATGGCA[C/T]GATCATGGCTCACTG	84708

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