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

LRSAM1

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs368892104	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127449941	CCTCCTAAGTGCCCA[C/T]GTGCTTAAGGAGGGG	90678
rs368916907	in-del	-/A	0.00398564	0.0444627	intron-variant	LRSAM1	GRCh38.p7	9:127485462	CTCGGGAGGCTGAGG[-/A]GGAGAATGGCGGGAA	90678
rs368942319	snp	A/G	0.000153988	0.00877328	utr-variant-5-prime, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451341	CGGCTGGTGTCGGAT[A/G]AACCCGGATTCGGGA	90678
rs368986687	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127458851	GAAGGAAAATGAGGC[A/G]GGAATGATCAACACT	90678
rs368989509	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127478678	GGCTGCATCCCAGAA[C/G]TGTCTTGAAGAGCCC	90678
rs369000621	snp	A/G	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127487220	CAAGATGGTGCCAAA[A/G]CACAAACATACGTGA	90678
rs369031677	snp	A/G	0.00318978	0.0398085	intron-variant	LRSAM1	GRCh38.p7	9:127500310	AGGTTGCAGTGAGCC[A/G]AGATCGCGCCACTGA	90678
rs369040356	snp	C/T	0.00398564	0.0444627	intron-variant	LRSAM1	GRCh38.p7	9:127482183	AGTCTCACTCTGTCA[C/T]CCAGGCTGGAGTGCA	90678
rs369062223	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127483825	ACACCACCACACCAG[C/G]CTAATTTTTGTATTT	90678
rs369070033	snp	C/G/T	0.00138019	0.0262361	synonymous-codon, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451309	GTTGGGGTCGAACTT[C/G/T]GGCGGCATGGTGGAG	90678
rs369138759	snp	A/G	0.00159617	0.0282053	intron-variant	LRSAM1	GRCh38.p7	9:127498638	TGCTCAGGGCTTCCT[A/G]CTTGTGCCCATTGGC	90678
rs369142922	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127477683	AGAGCCCAGGAGGTC[A/G]CGGCTGCAGTGAGCT	90678
rs369153994	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127461778	CACAGGCGCCTTACC[C/T]GCAGGAGCGCTCTGC	90678
rs369161790	snp	C/G	4.98633e-05	0.00499291	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127497327	GGATGCAGCCAGGAT[C/G]CAGCCAGGTACAAGC	90678
rs369169581	snp	C/T	9.8987e-05	0.00703447	intron-variant	LRSAM1	GRCh38.p7	9:127473953	CAAGGCAGCCTGCTG[C/T]ACGCATACATGTGTG	90678
rs369183416	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127489076	CTCCATTTCTCAGAG[A/G]AGGCATCTGCCTTGT	90678
rs369250629	snp	A/G	0.000153988	0.00877328	intron-variant	LRSAM1	GRCh38.p7	9:127454977	GTCTTAATACTTTTT[A/G]AAAATTCTTTTTATC	90678
rs369322567	snp	G/T			intron-variant	LRSAM1	GRCh38.p7	9:127473283	ACCAGTTACCACCTG[G/T]AAGAAGATAGTTACA	90678
rs369353985	snp	C/T	0.000165079	0.00908363	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127479962	CGGATCCAGAAGCTG[C/T]TGCAGGACAATCAGA	90678
rs369359462	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127467446	GTTATGCCCTTAAGG[A/G]AGGGAGGGAAGGGGG	90678
rs369384290	snp	C/T	1.64754e-05	0.00287009	intron-variant	LRSAM1	GRCh38.p7	9:127455570	CTCTTCTTTATCTTA[C/T]CTTAGATTCCATTTG	90678
rs369401880	snp	C/T	2.78734e-05	0.00373308	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127489446	GTCTGTGTTGCAGAG[C/T]GCGATGCAGAAGGCT	90678
rs369421796	snp	A/T			intron-variant	LRSAM1	GRCh38.p7	9:127467387	CACCTCAATATCTTA[A/T]CAGTAAGTGCATTCC	90678
rs369439346	snp	A/G	0.000298033	0.0122036	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127489502	AAGACCTGATGCATC[A/G]GCAGATCAGGAGCCA	90678
rs369471343	snp	A/T			intron-variant	LRSAM1	GRCh38.p7	9:127457124	CTTTCACCCTTGAAG[A/T]TCCAGGTTTTAAGGA	90678
rs369492293	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127496827	GTCACAAGGCCATGC[C/T]GCTCAGGCTCTGGAG	90678
rs369526105	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127497842	ATGATCTGGGAGCCC[A/G]GCACCTGCCCACCGC	90678
rs369532729	in-del	-/T			intron-variant	LRSAM1	GRCh38.p7	9:127488433	GCCCAACTAATTTTT[-/T]GTATTTTTAGTAGAG	90678
rs369538067	in-del	-/C	0.0111196	0.0737302	intron-variant	LRSAM1	GRCh38.p7	9:127495165	TCCATGTTGGTCAGG[-/C]TGGTCTTGAACTCCC	90678
rs369551479	snp	G/T			intron-variant	LRSAM1	GRCh38.p7	9:127496888	GCTGCTTAGTGGCTT[G/T]GCCTCCAAGGCTTCT	90678
rs369596022	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127459759	AGACTTGTTTTCACC[A/G]TGTTGGCCAGGCTGA	90678
rs369596799	snp	A/G	0.000153988	0.00877328	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127483006	CTGAGAGCCTGCGGC[A/G]ACGTGACGTTGCCTG	90678
rs369718525	snp	A/C			intron-variant	LRSAM1	GRCh38.p7	9:127502316	GTTACCTGTTTCGGC[A/C]GTGCCTGTTCTGTTT	90678
rs369757653	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127467395	TATCTTATCAGTAAG[C/T]GCATTCCTGGATGTG	90678
rs369813487	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127472461	ACCTTTACCAACATG[C/T]GGAAACCCTGTCTCT	90678
rs369816812	snp	C/T	0.000629349	0.0177279	intron-variant	LRSAM1	GRCh38.p7	9:127467697	TGTGGTCTCCGGTTG[C/T]GTTGGTAGCGAACAG	90678
rs369818709	snp	A/C	5.27079e-05	0.00513334	intron-variant	LRSAM1	GRCh38.p7	9:127495921	TGTAAACAGTGGGTT[A/C]TTTTCTTCCTTCCTG	90678
rs369922065	snp	C/T	0.00279162	0.0372561	intron-variant	LRSAM1	GRCh38.p7	9:127467128	TGCTCAAAATTCTCT[C/T]GGCCCTGAGGAAGGG	90678
rs369922504	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127459322	CTCCCGAGTTCAAGC[A/G]ATTCTCCTGCCTCAG	90678
rs369939320	snp	C/T	1.65899e-05	0.00288005	missense, intron-variant, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127491246	CTGAGTTATTGCAGC[C/T]GACACAGCTGGAGTT	90678
rs369968003	snp	A/C/G	0.000181229	0.00951763	intron-variant	LRSAM1	GRCh38.p7	9:127473790	GTCAGCTTGTGTCCC[A/C/G]TCTCTTACAGAGTCA	90678
rs370005236	snp	C/G	1.74027e-05	0.00294975	intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127449577	TACCTGTCCCCCCAC[C/G]CTCCTCTCCCGAAAC	90678
rs370037784	snp	C/G	3.09009e-05	0.00393059	intron-variant	LRSAM1	GRCh38.p7	9:127489540	GCTGGGGCTGGGGTC[C/G]CTGGACCTGCTCTCT	90678
rs370051450	snp	C/T	0.000202333	0.0100561	intron-variant	LRSAM1	GRCh38.p7	9:127483051	GGGAGCTTGTGAGCA[C/T]GCTGCCTGCTGGCTG	90678
rs370184825	snp	A/T			intron-variant	LRSAM1	GRCh38.p7	9:127467228	AGCAGAACTGGCAAA[A/T]AGTTAAAAAATTAAT	90678
rs370239731	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127476020	GCTGGGATTACAGGT[C/G]TGAGCCACCACACCC	90678
rs370328910	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127473136	GAATATTTTTCATAC[A/G]TCTCCTGCCCATTTT	90678
rs370358510	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127503269	GGCCATGCACAGGCC[C/T]GTCCCACCCTGCATG	90678
rs370363137	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127490324	CTTTAATTTCAATTC[C/T]ACATTGCCGGACATG	90678
rs370365661	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127485329	TTGGGAGGCCAAGGC[A/G]GGTGGATCACGAGGT	90678
rs370404396	snp	C/T	0.00318978	0.0398085	intron-variant	LRSAM1	GRCh38.p7	9:127495180	CTGGTCTTGAACTCC[C/T]GACCTCAGGTGATCT	90678
rs370413860	snp	A/G			upstream-variant-2KB, intron-variant	RPL12, LRSAM1	GRCh38.p7	9:127453143	CTGGAGTGCAGTGGC[A/G]TGATCTTGGCTCACT	90678
rs370424479	snp	A/G	0.000103822	0.00720419	intron-variant	LRSAM1	GRCh38.p7	9:127479793	AGTACCCCTCACGGC[A/G]TCTGAGGGGGTCCCA	90678
rs370432455	in-del	-/TG			intron-variant	LRSAM1	GRCh38.p7	9:127497941	TCAAGATGGGGAAAC[-/TG]AAGCGCAAAGAGGTT	90678
rs370434770	snp	C/G	1.64961e-05	0.00287189	intron-variant	LRSAM1	GRCh38.p7	9:127479348	TAACTCCCCCAGGGC[C/G]TGTGCTGACAGTCAC	90678
rs370502826	snp	A/G/T	0.000156575	0.00884686	intron-variant	LRSAM1	GRCh38.p7	9:127467841	CAAAGGTAAAGCCAG[A/G/T]CCGCTGCCTCCTCCC	90678
rs370511765	snp	A/G	0.00597247	0.0543191	intron-variant	LRSAM1	GRCh38.p7	9:127458314	GTGAACCCGGGAAGC[A/G]GAGCTTGCAGTGAGC	90678
rs370536935	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127489777	TCTCCACCACGCCTG[A/G]GCCAGGGAGGCTGGT	90678
rs370608535	snp	A/C	1.75872e-05	0.00296535	intron-variant	LRSAM1	GRCh38.p7	9:127485886	TGGGGGAGCTGGCTC[A/C]GGGCCCAAGACCGTG	90678
rs370672170	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127490427	CAGGATAGAGAAGTA[C/T]TGGCTATGGGGTCTG	90678
rs370737592	snp	C/G/T	5.93752e-05	0.00544836	intron-variant	LRSAM1	GRCh38.p7	9:127492770	GCGCTGCCGCCAGCT[C/G/T]ACGGTGGTGCGGGGT	90678
rs370745787	snp	A/C/T	5.15897e-05	0.00507864	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127495974	TGCAGGAAGAGGGGA[A/C/T]GGAGCGCCAGCTGGT	90678
rs370749855	in-del	-/G	0	0	upstream-variant-2KB, intron-variant	RPL12, LRSAM1	GRCh38.p7	9:127452330	AGGGACGGATGGGGG[-/G]AGGGCTGTTTTCAAA	90678
rs370754350	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127499099	AATATAGAAGCTGGG[C/T]GCAGTGGCTCATGGC	90678
rs370797643	snp	A/G	0.000798403	0.0199641	intron-variant, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127487619	CAAGGGGCCTGGCAC[A/G]TAGTAGGTGCTCGGG	90678
rs370840977	snp	C/T	4.97863e-05	0.00498906	intron-variant	LRSAM1	GRCh38.p7	9:127500968	AGGGGTTAGGGTCAG[C/T]GGAGATGACCCTGGC	90678
rs370872133	snp	A/G	0.000156864	0.0088548	intron-variant	LRSAM1	GRCh38.p7	9:127492798	GGTGTGGTCTTGTTC[A/G]CAGGAGATGATCTCG	90678
rs370881098	snp	A/G	0.000153988	0.00877328	intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127449723	ACTAGAAATAAAGGC[A/G]TGTAATCAACATGGT	90678
rs370901849	snp	C/G/T			intron-variant	LRSAM1	GRCh38.p7	9:127467467	GGGAAGGGGGCTGCA[C/G/T]GTGAAGAAACTAAAA	90678
rs370979778	snp	A/T			intron-variant	LRSAM1	GRCh38.p7	9:127499539	CTGTCTAAAAAAAAA[A/T]ATATATATATATATA	90678
rs371087432	snp	G/T			intron-variant	LRSAM1	GRCh38.p7	9:127464098	TTCCGGAGTGGCCTG[G/T]AGTTGACCCCACTCT	90678
rs371146474	snp	A/G/T	6.1566e-05	0.00554796	intron-variant	LRSAM1	GRCh38.p7	9:127454645	TCCCATCTCCTCCTC[A/G/T]GTCCCCATGGAGTAG	90678
rs371152397	in-del	-/T	0.0672332	0.170576	intron-variant	LRSAM1	GRCh38.p7	9:127481256	CAGGGGAGGGCAGCA[-/T]TTTTTTTTTTTTTTT	90678
rs371175016	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127497647	ACACACTGAGGGACT[C/T]TGGACTAGAGGGAGA	90678
rs371175866	snp	C/T	0.000153988	0.00877328	intron-variant	LRSAM1	GRCh38.p7	9:127478888	CCATGCCAGGGAGAA[C/T]CACTGCTGCCACCCT	90678
rs371240206	snp	C/G	1.68539e-05	0.00290287	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127496050	TGCGCACCACCGCCT[C/G]TCACTGGACCTGCTG	90678
rs371244535	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127465445	TGTAGCCAGCATCCT[A/G]GTATAGCCCACAGTC	90678
rs371256717	snp	C/G	0.000472321	0.0153603	intron-variant	LRSAM1	GRCh38.p7	9:127497367	GCCTCTTCCAGGCAG[C/G]GCTCCAGCCGTATGT	90678
rs371308201	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127495854	TTGTAGGAAAAATCC[C/T]GAGTACATTCTATGT	90678
rs371335734	snp	A/T			intron-variant	LRSAM1	GRCh38.p7	9:127484421	CAGGCTGGAGGGCAG[A/T]GGTGTGAACCTGCTC	90678
rs371374976	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127487308	GAGTGCCGGGAAGGA[C/T]AGCTTTGTCATACTT	90678
rs371417350	snp	C/T	0.00993419	0.0697739	intron-variant	LRSAM1	GRCh38.p7	9:127464380	CCGTGCTGTCCAGAG[C/T]GGCGGCCACTGGCCA	90678
rs371422360	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127474380	TTAAGTGATCCTCCC[A/G]CCTCAGACTCCCAAA	90678
rs371533252	snp	A/G	0.000148688	0.00862101	intron-variant	LRSAM1	GRCh38.p7	9:127454957	CCACTCTGCAAAGGT[A/G]TTTTGTCTTAATACT	90678
rs371583120	snp	A/T			intron-variant	LRSAM1	GRCh38.p7	9:127456416	TTTTTGTATTTTTAG[A/T]GATGAGGTTTTGCCA	90678
rs371613517	snp	C/T	0.000153988	0.00877328	intron-variant	LRSAM1	GRCh38.p7	9:127501151	AACGGGAGGTAAGTC[C/T]GGGGCCCTCCCCACC	90678
rs371704685	snp	G/T			intron-variant	LRSAM1	GRCh38.p7	9:127488329	TGCAGTGGTGCGATC[G/T]CGGCTCACTGCAACC	90678
rs371724522	snp	A/C/T	0.00179796	0.0299304	intron-variant	LRSAM1	GRCh38.p7	9:127467718	TAGCGAACAGTAAAG[A/C/T]GGGTTACCCTTGTGT	90678
rs371770495	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127466201	ATAGTTCCAGCTACT[C/T]GGGAGGCTGAGGCAA	90678
rs371799194	snp	C/T	1.69683e-05	0.00291271	intron-variant	LRSAM1	GRCh38.p7	9:127495292	ATTACCATTTTGTGA[C/T]TAACATTGCCTGCTT	90678
rs371855325	in-del	-/GTGGCTCATGCCTGTAATCCCAG			intron-variant	LRSAM1	GRCh38.p7	9:127456616	TGCCTGTAATCCCAG[-/GTGGCTCATGCCTGTAATCCCAG]CACTTCGGGAGGCCG	90678
rs371865387	snp	A/G	5.17585e-05	0.0050869	synonymous-codon, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127450788	ACCGACTTCACCTCC[A/G]GTGCACCTCAGGTAT	90678
rs371872032	snp	C/T	0.00067914	0.0184149	intron-variant	LRSAM1	GRCh38.p7	9:127495442	TGCTGGTGCCTGTCC[C/T]GGCCAGGGAGCCCTG	90678
rs371929794	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127471529	CGGTGGCTCACGCCT[C/G]TAATCCCAGCACTTT	90678
rs371954055	snp	C/T	0.000243415	0.0110294	intron-variant	LRSAM1	GRCh38.p7	9:127496139	AGGGGCACGCAAGGC[C/T]GCTGTCCTGACCAGC	90678
rs371972404	in-del	-/GGGTA			intron-variant	LRSAM1	GRCh38.p7	9:127499424	CATCCCAGCTACTCT[-/GGGTA]GGAGGCTGAGGTAGG	90678
rs371977635	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127481821	AGCACTTTGGGAGGC[C/T]GAGGTGGGCAGATCA	90678
rs372040839	snp	A/G/T	0.000140672	0.00838568	utr-variant-3-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127502909	AGCTGAGTGCTGCCC[A/G/T]CCCACCTGGGCCTGG	90678
rs372048865	snp	G/T			intron-variant	LRSAM1	GRCh38.p7	9:127462675	CAGTGAGGCCTGTCG[G/T]AGGAGGGTGGTGGGG	90678
rs372061853	in-del	-/CCTCCTGAA			intron-variant	LRSAM1	GRCh38.p7	9:127483916	GATCGCCTGCCTCAA[-/CCTCCTGAA]GTGCTGGTATTACAG	90678
rs372077339	snp	A/G			intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127449976	TTCAGCCCTGCTGAC[A/G]TTAGAATCACCTAAG	90678
rs372112782	snp	A/C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127461338	ACAGGCTGCCCCGCC[A/C/T]GGGAGCCATTGAGCA	90678
rs372178158	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127486920	GGGCGCAGTGGCTCA[C/T]GTCTGTAATCCCAGC	90678
rs372198512	snp	A/G/T	5.34053e-05	0.00516723	intron-variant	LRSAM1	GRCh38.p7	9:127481278	TTTTTTTTTGAGACG[A/G/T]AGTCCTGCACTGTCG	90678
rs372209329	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127474276	TTTTTTTTTTTTTTT[C/T]CCTTTTTTTGAGACA	90678
rs372244339	snp	A/G	1.64727e-05	0.00286986	intron-variant	LRSAM1	GRCh38.p7	9:127455065	CAGAGGTAAACTGAG[A/G]ATAGTGTTGGGCTGT	90678
rs372273035	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127496907	TCCAAGGCTTCTCTC[C/G]TCCCCCACCTGGTGG	90678
rs372357453	snp	A/G	4.95323e-05	0.00497631	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127479438	TGGAACTGGGGCAGC[A/G]GGAGCACACCCAGCT	90678
rs372376747	snp	G/T			intron-variant	LRSAM1	GRCh38.p7	9:127459497	GTGCTGGGATTACAG[G/T]TGTGAGCCACCACGC	90678
rs372408222	snp	A/G	6.77335e-05	0.00581912	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127454589	AACGCCTGGAGTACC[A/G]GATGTGTTTGGTGAG	90678
rs372423898	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127499856	CTTGAATCCAGGAGG[C/T]GGAGGTTGCAGTGAG	90678
rs372433819	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127467664	TGACAGAGAACACAC[A/G]AATTGATAAGGAAAT	90678
rs372437126	snp	C/T	0.00478085	0.0486577	intron-variant	LRSAM1	GRCh38.p7	9:127455139	AAGACAGAGGTGGAC[C/T]GGGGCTTTAGAAAGG	90678
rs372452916	snp	A/G	3.6626e-05	0.00427921	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127487680	CTTTCTGGCAGCATG[A/G]CCGAAATGGATGAAC	90678
rs372458173	snp	C/T	0.00318978	0.0398085	intron-variant	LRSAM1	GRCh38.p7	9:127465830	GTCAGAGGTTGGCAG[C/T]GGGAGGGCAGGGTCC	90678
rs372460631	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127486540	GCCACCCTCCAGGGC[A/G]CCTGGACTGTGCGGG	90678
rs372491221	in-del	-/TTTG			intron-variant	LRSAM1	GRCh38.p7	9:127493077	TTTTTTATTTGTTTG[-/TTTG]AGACAGGGTCTCACT	90678
rs372509526	snp	A/T	0.000254586	0.0112795	intron-variant	LRSAM1	GRCh38.p7	9:127489533	GGTGAGCGCTGGGGC[A/T]GGGGTCCCTGGACCT	90678
rs372513813	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127483166	TGCCATGGAGCACAG[A/G]CTCTGGGGTCAGCCT	90678
rs372576882	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127461316	TGGGCCATCCTGGCC[A/G]GGATCCACAGGCTGC	90678
rs372706812	snp	C/T	5.17531e-05	0.00508664	utr-variant-5-prime, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451345	TGGTGTCGGATGAAC[C/T]CGGATTCGGGACGAC	90678
rs372711801	snp	C/T	0.000104049	0.00721203	intron-variant	LRSAM1	GRCh38.p7	9:127492756	ACTGCGGGACTCCTG[C/T]GCTGCCGCCAGCTCA	90678
rs372719192	snp	G/T			intron-variant	LRSAM1	GRCh38.p7	9:127463061	AATTATCCAGGCGTG[G/T]TGGTGCGCACCTGTA	90678
rs372809141	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127483819	AGATGCACACCACCA[C/T]ACCAGGCTAATTTTT	90678
rs372834793	snp	G/T			intron-variant	LRSAM1	GRCh38.p7	9:127457141	CCAGGTTTTAAGGAA[G/T]GGCATTAGATTCCCC	90678
rs372845307	snp	G/T	0.00199481	0.0315187	intron-variant	LRSAM1	GRCh38.p7	9:127456238	AAGTTTTGTTTGTTT[G/T]TTTTTTTTTTTGAAG	90678
rs372859811	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127494062	CAGATGGTGCCTTGG[C/T]GCTGTGCCTTAGCAG	90678
rs372873701	snp	C/T	1.74928e-05	0.00295738	intron-variant	LRSAM1	GRCh38.p7	9:127492916	TGTGTTTGGCTTCTG[C/T]GCTCAGCATCACACA	90678
rs372890516	snp	A/G	6.68014e-05	0.00577895	intron-variant	LRSAM1	GRCh38.p7	9:127457290	CTCTTCCTCAGCCCA[A/G]CATGGCCGCACATCT	90678
rs372951191	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127496862	AGGGACTGTGGGGCT[C/G]GTGTGCTGCTGCTGC	90678
rs372964730	snp	G/T	0.00318978	0.0398085	intron-variant	LRSAM1	GRCh38.p7	9:127457898	CACAGGCCCAATCTG[G/T]TATACTATATTGTTT	90678
rs372970231	snp	G/T	0.000153988	0.00877328	intron-variant	LRSAM1	GRCh38.p7	9:127485861	GAAGAGGAGTCCCAG[G/T]TGAGGGAGCTGGGGG	90678
rs372988985	in-del	-/A			intron-variant	LRSAM1	GRCh38.p7	9:127465078	GATCTTCAGGTGTCA[-/A]CGCACGCCACCCACC	90678
rs373004271	snp	C/G	6.62822e-05	0.00575645	intron-variant	LRSAM1	GRCh38.p7	9:127485703	CCAGGAGCAGCCACT[C/G]CACTCAGCTGTCCCC	90678
rs373015900	snp	C/T	0.000148271	0.00860893	intron-variant	LRSAM1	GRCh38.p7	9:127473798	GTGTCCCGTCTCTTA[C/T]AGAGTCAGGGCTGGA	90678
rs373030898	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127484640	TGCTTATATTACAGG[C/T]GAGCCGCCATGTCCA	90678
rs373040143	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127467388	ACCTCAATATCTTAT[C/T]AGTAAGTGCATTCCT	90678
rs373087015	snp	A/G			upstream-variant-2KB, intron-variant	RPL12, LRSAM1	GRCh38.p7	9:127453042	CTGTACAGCCAGGCC[A/G]CTGAACTTAATAAGC	90678
rs373152123	snp	C/G	0.000153988	0.00877328	intron-variant	LRSAM1	GRCh38.p7	9:127491167	CAGCACAAAACTGAA[C/G]TGTGGTTAATGTGAG	90678
rs373156612	snp	A/T	1.64789e-05	0.0028704	intron-variant	LRSAM1	GRCh38.p7	9:127455630	AAGAAGGTAAGATGG[A/T]GCTTCATCTTCAGAG	90678
rs373194876	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127479189	GGTTGAGCCCAGCAC[C/T]GGGCTCTAGACCACT	90678
rs373240847	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127468100	TGGCTCCACTGACAC[A/G]GAGTCATGGTTAAGA	90678
rs373307015	in-del	-/T/TT	0.407502	0.194147	intron-variant	LRSAM1	GRCh38.p7	9:127459217	CTTGGCCCTTTGGGG[-/T/TT]TTTTTTTTTTTTTTT	90678
rs373347890	in-del	-/A			intron-variant	LRSAM1	GRCh38.p7	9:127467232	AACTGGCAAAAAGTT[-/A]AAAAAATTAATTGGT	90678
rs373392828	in-del	-/GT	0.00318978	0.0398085	intron-variant	LRSAM1	GRCh38.p7	9:127466429	AATATGAATGTGAAA[-/GT]GTATGAATATATTAT	90678
rs373426038	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127498876	CCAGCCTGGCCAACA[C/T]GGTGAAACCCTGTCT	90678
rs373443912	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127478570	GTATTTTGGTGGACT[A/G]GAACCGGGTGCTGTA	90678
rs373463905	in-del	-/A			intron-variant	LRSAM1	GRCh38.p7	9:127467268	AGCAGTTACAAAAAA[-/A]TAAACAGTTCCAGGT	90678
rs373494551	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127467396	ATCTTATCAGTAAGT[A/G]CATTCCTGGATGTGC	90678
rs373498848	snp	C/G	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127500785	AGCGCTGCGGCCATC[C/G]CTGCAGAGAGAGACT	90678
rs373515438	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127468713	AGACATGGTGGCTTG[C/T]GCCTGTAATCCCAGC	90678
rs373532339	snp	C/T	0.000111439	0.00746373	intron-variant	LRSAM1	GRCh38.p7	9:127489548	TGGGGTCCCTGGACC[C/T]GCTCTCTCAGAGACT	90678
rs373570877	snp	A/G	0.000372675	0.0136455	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127483014	CTGCGGCGACGTGAC[A/G]TTGCCTGTGAGTTTT	90678
rs373571535	snp	G/T	1.65157e-05	0.0028736	splice-donor-variant	LRSAM1	GRCh38.p7	9:127479979	GCAGGACAATCAGAG[G/T]TTGGGCTCTGCTCCT	90678
rs373581021	snp	C/T	8.75894e-05	0.00661718	intron-variant	LRSAM1	GRCh38.p7	9:127495934	TTCTTTTCTTCCTTC[C/T]TGCTCATGGTACACG	90678
rs373669417	snp	A/C/G	3.30826e-05	0.00406699	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127457386	TCCTGAGTCTGGCAA[A/C/G]CATCAAGGTACTGGG	90678
rs373695521	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127488907	CTCTTTCCTGCAGCC[C/T]CGTGGGAGTCTTGCC	90678
rs373746396	snp	C/T			intron-variant, utr-variant-5-prime	LRSAM1	GRCh38.p7	9:127454063	TAGAAAGACGCAGCC[C/T]CTGCCCCCGTGGAAC	90678
rs373768842	snp	C/T	0.0023933	0.0345097	downstream-variant-500B	LRSAM1	GRCh38.p7	9:127503755	CTGTGCCTCCATGAG[C/T]GGAGGAGCCCTGTGT	90678
rs373773839	snp	G/T			intron-variant	LRSAM1	GRCh38.p7	9:127485530	CACTGCACTCCAGCC[G/T]GGGTGACAGAGTGAG	90678
rs373798552	snp	A/G	0.000358389	0.0133816	intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127449588	CCACCCTCCTCTCCC[A/G]AAACCAAGCACAAGC	90678
rs373871150	snp	C/T	5.17853e-05	0.00508822	intron-variant	LRSAM1	GRCh38.p7	9:127479805	GGCGTCTGAGGGGGT[C/T]CCAGGGGCTCAGGAC	90678
rs373913471	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127497170	GTCGACGGTCCTGTG[A/G]GCCTGGGCCTGTGCC	90678
rs373990000	snp	C/T	0.000455615	0.0150864	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127502866	GTGCCGCCAGGACAT[C/T]GCCCAGCGCCTCCGC	90678
rs374043025	snp	A/G	0.000148607	0.00861866	intron-variant	LRSAM1	GRCh38.p7	9:127458975	GGACTTTCTCACTTG[A/G]AGACTCACAGGGGTC	90678
rs374054572	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127496117	AGCAGCCGTCTGCAT[A/G]GAGGGGAGGGGCACG	90678
rs374055807	snp	A/G			upstream-variant-2KB, intron-variant	RPL12, LRSAM1	GRCh38.p7	9:127452151	GCATCTAGGCTGGAC[A/G]TCGGAGAGGGAGGGA	90678
rs374058539	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127467174	ATACTGTGGTCTAAA[C/T]AGGGGAGGGGGGAGT	90678
rs374063879	snp	A/C/T	3.4225e-05	0.00413661	intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451262	ATCCCGCAGCCCCGG[A/C/T]CACAACCAGAGCACG	90678
rs374173402	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127479126	TCACATGCCTCAGGT[C/G]GGTGGTAGAGCATCC	90678
rs374192112	snp	C/T	0.00358779	0.0422022	intron-variant	LRSAM1	GRCh38.p7	9:127497665	GACTAGAGGGAGAAA[C/T]AGCCCGTCCCCAGGG	90678
rs374225890	in-del	-/G			intron-variant	LRSAM1	GRCh38.p7	9:127462705	GAGGGAGAGCATCAG[-/G]AAGAAAAGCTAATGG	90678
rs374258145	snp	A/G	0.000164747	0.0090745	intron-variant	LRSAM1	GRCh38.p7	9:127478893	CCAGGGAGAACCACT[A/G]CTGCCACCCTCTCTT	90678
rs374268207	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127485947	CTGGGCCACCCCAGC[C/T]TCTGCTCTGCTGTTA	90678
rs374296150	snp	C/T	0.000872832	0.0208723	intron-variant	LRSAM1	GRCh38.p7	9:127495279	TATTACAGGTTTTAT[C/T]ACCATTTTGTGACTA	90678
rs374299426	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127475407	GAGGCACAAGAATCA[C/T]TTGAATCCAGGAGGC	90678
rs374316567	snp	C/T			upstream-variant-2KB, intron-variant	RPL12, LRSAM1	GRCh38.p7	9:127452150	CGCATCTAGGCTGGA[C/T]GTCGGAGAGGGAGGG	90678
rs374344308	snp	A/G	0.000208863	0.010217	intron-variant	LRSAM1	GRCh38.p7	9:127467698	GTGGTCTCCGGTTGC[A/G]TTGGTAGCGAACAGT	90678
rs374350858	snp	A/G	9.34973e-05	0.00683666	intron-variant	LRSAM1	GRCh38.p7	9:127501168	GGGCCCTCCCCACCC[A/G]CCTGCCCTGCCTGTG	90678
rs374369472	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127490882	TCTGTCTGTGCTTTA[C/G]TCTGGCCTGAATCCC	90678
rs374425517	snp	C/T	1.68451e-05	0.00290211	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127496060	CGCCTCTCACTGGAC[C/T]TGCTGAGCCAAATGA	90678
rs374436016	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127489728	AGAGACCTCCTATTC[C/T]GGGGTCTGGCGAGGG	90678
rs374449653	snp	C/T	8.55264e-05	0.0065388	intron-variant	LRSAM1	GRCh38.p7	9:127496108	AAGGTGGGCAGCAGC[C/T]GTCTGCATGGAGGGG	90678
rs374499036	snp	A/G	1.93142e-05	0.00310752	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127487763	CCAGATCCTGCAGGA[A/G]GTGAGCCCTCGCCCA	90678
rs374662909	snp	C/T	5.20531e-05	0.00510135	intron-variant	LRSAM1	GRCh38.p7	9:127479789	AGTCAGTACCCCTCA[C/T]GGCGTCTGAGGGGGT	90678
rs374734912	snp	A/G	0.000541523	0.0164459	intron-variant	LRSAM1	GRCh38.p7	9:127489570	TCAGAGACTTGCAGA[A/G]TGGCCCTCCAGGGCG	90678
rs374756755	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127470675	TGTGTGGATACCACA[C/T]GGCAAGTGGAAAGAA	90678
rs374805982	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127467394	ATATCTTATCAGTAA[C/G]TGCATTCCTGGATGT	90678
rs374810801	snp	C/T	3.43377e-05	0.00414339	intron-variant	LRSAM1	GRCh38.p7	9:127497369	CTCTTCCAGGCAGGG[C/T]TCCAGCCGTATGTGT	90678
rs374840100	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127501775	ATTCATTAACACTTA[C/T]TCTAAAAATTACACA	90678
rs374845304	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127491762	GGGGCTCCAGCCCGG[A/G]AGTCCTGCGCACACA	90678
rs374848673	snp	C/T	1.64762e-05	0.00287016	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127461181	TTCTTAGGTCTTAAA[C/T]GTGGAAAGGAATCAA	90678
rs374878421	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127459724	CCACCACACCTGGAC[A/G]ATTTTTGTATTTTCA	90678
rs374895470	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127480317	TATTTTGGGTTCTGC[A/G]TAACCCGTTGCACTG	90678
rs374907938	in-del	-/AACA			intron-variant	LRSAM1	GRCh38.p7	9:127475512	ACAAACAAACAAACA[-/AACA]TTTAAAAATGCCAAC	90678
rs374918675	snp	A/G	3.32281e-05	0.0040759	intron-variant	LRSAM1	GRCh38.p7	9:127459101	ACAGAAACCCACCTC[A/G]GATGGCCTTAGTGAG	90678
rs374994721	snp	G/T			intron-variant	LRSAM1	GRCh38.p7	9:127500023	CAGGAAGGGAACGAG[G/T]GATAGAGTCAAGGAA	90678
rs375139081	snp	A/C/G	0.00011359	0.00753555	intron-variant, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127487632	ACATAGTAGGTGCTC[A/C/G]GGAAACGTTCCAAGA	90678
rs375143572	snp	C/T	2.45806e-05	0.00350567	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127467749	CTGCAGATGCTGAGC[C/T]TTGACGCCTCGGCCA	90678
rs375181027	snp	G/T			intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127450119	AACAGGAGGCTAAGT[G/T]TCCCTTAAGTGCCAG	90678
rs375184961	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127458056	CATGTATAAATATTT[C/T]TCCAAGGCCTTTTTT	90678
rs375198479	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127478595	GCTGTAGGTGTGTTA[C/T]GCAGACATCCATGGG	90678
rs375221138	in-del	-/A			intron-variant	LRSAM1	GRCh38.p7	9:127470376	AACCATCAGATCTTG[-/A]TGAGAACTCACCCAC	90678
rs375244765	snp	A/C/G	0.00022498	0.0106039	intron-variant	LRSAM1	GRCh38.p7	9:127495457	CGGCCAGGGAGCCCT[A/C/G]GGGACCTCCTCCCAG	90678
rs375299102	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127499857	TTGAATCCAGGAGGC[A/G]GAGGTTGCAGTGAGC	90678
rs375300595	snp	G/T			intron-variant	LRSAM1	GRCh38.p7	9:127498593	GGCCATGAGGATCTG[G/T]GGCCACATGCAGAAA	90678
rs375352442	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127492713	GAGAACCGAGTGAGC[A/G]GGAGGCCAGGCCCTT	90678
rs375474640	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127466059	CAAGCTTGTAATCCT[A/G]GCACTTTGGGAAGAC	90678
rs375477771	snp	G/T			intron-variant	LRSAM1	GRCh38.p7	9:127494988	CGGAGTTTCGCTCTT[G/T]TTGCCCAGGCTGGAG	90678
rs375515782	snp	A/G	3.30164e-05	0.00406289	intron-variant	LRSAM1	GRCh38.p7	9:127461283	AGAAGCCGTGTCCGT[A/G]TGACCCTCCATCAGC	90678
rs375537151	snp	A/G	3.29522e-05	0.00405894	intron-variant	LRSAM1	GRCh38.p7	9:127455525	CCACTCAGAGAACAA[A/G]CTAAAAACTGGCAGG	90678
rs375553287	snp	A/G	0.00953873	0.0683987	intron-variant	LRSAM1	GRCh38.p7	9:127465665	GCTGGCCAGGGCTGG[A/G]GGACCTGAGCTACCC	90678
rs375559702	in-del	-/TATT			upstream-variant-2KB, intron-variant	RPL12, LRSAM1	GRCh38.p7	9:127453089	ATTTATTTATTTATT[-/TATT]ATTATTTTCTGAGAC	90678
rs375619104	snp	C/T	0.000211101	0.0102716	intron-variant	LRSAM1	GRCh38.p7	9:127489539	CGCTGGGGCTGGGGT[C/T]CCTGGACCTGCTCTC	90678
rs375636993	snp	A/G	3.30486e-05	0.00406487	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127479451	GCGGGAGCACACCCA[A/G]CTCCTTCAGCAGAGC	90678
rs375737634	snp	C/T	5.08617e-05	0.00504264	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127492820	ATGATCTCGGAGCAG[C/T]GCTGGGCCCTCAGCT	90678
rs375876334	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127456014	AGGCTTATGAACCCC[A/G]GTGTTAGTAATAATA	90678
rs375937623	snp	G/T	3.90236e-05	0.00441705	intron-variant	LRSAM1	GRCh38.p7	9:127487766	GATCCTGCAGGAGGT[G/T]AGCCCTCGCCCAGAG	90678
rs375938990	snp	C/G/T	1.65954e-05	0.00288053	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127497292	CAGCACGAGATCCTC[C/G/T]GGAGAGTCCAGGAAC	90678
rs375949142	snp	G/T	1.84323e-05	0.00303576	intron-variant	LRSAM1	GRCh38.p7	9:127454626	TGGGTTTCCTCTAAC[G/T]CTATCCCATCTCCTC	90678
rs376016199	snp	C/T			upstream-variant-2KB, intron-variant	RPL12, LRSAM1	GRCh38.p7	9:127453191	GGTTCAAGCAATTCT[C/T]GTTCCTCAGCCTTCC	90678
rs376118759	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127457699	CCAGGCAAGAAGGAA[A/G]AGGAGGGACGCGCAG	90678
rs376141459	snp	A/C			intron-variant	LRSAM1	GRCh38.p7	9:127489016	TTCAATCTCTGTTCT[A/C]AAATGGTTTGACTTA	90678
rs376196543	snp	A/C			intron-variant	LRSAM1	GRCh38.p7	9:127465996	CTGTATATTGTAAAA[A/C]AAAAAAAATGCAAAT	90678
rs376247483	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127463658	AAGATGCTATCTCCA[C/T]ATACAGCCACATTCT	90678
rs376307049	snp	C/T	1.8479e-05	0.0030396	intron-variant	LRSAM1	GRCh38.p7	9:127501189	CCTGCCTGTGGCCAC[C/T]CTCCTCAAATTCTGC	90678
rs376316410	snp	C/T	1.83977e-05	0.00303291	intron-variant	LRSAM1	GRCh38.p7	9:127491345	GTGGTGAGACCCCCA[C/T]CTGGTGCTCCCTCCC	90678
rs376362600	snp	A/C/T	5.01419e-05	0.00500688	intron-variant	LRSAM1	GRCh38.p7	9:127457287	CTGCTCTTCCTCAGC[A/C/T]CAGCATGGCCGCACA	90678
rs376368787	snp	G/T			upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	RPL12, LRSAM1	GRCh38.p7	9:127451647	GTGATCCCAGCCCTA[G/T]CTGTTTCCCATATTC	90678
rs376382147	snp	A/G	1.65701e-05	0.00287833	intron-variant	LRSAM1	GRCh38.p7	9:127491169	GCACAAAACTGAACT[A/G]TGGTTAATGTGAGTA	90678
rs376397014	snp	A/G	0.000132468	0.00813735	synonymous-codon, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127449688	TGCCTTGGCAATGTC[A/G]TCACCAACTTTTTTT	90678
rs376421929	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127458044	CCTGTGTGTGCACAT[A/G]TATAAATATTTCTCC	90678
rs376436763	snp	A/G	2.96248e-05	0.00384857	intron-variant	LRSAM1	GRCh38.p7	9:127483044	TGGGATGGGGAGCTT[A/G]TGAGCACGCTGCCTG	90678
rs376439091	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127463988	CGTTGTAAACCAGGC[C/T]GTCTGAAGCTGACGC	90678
rs376439307	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127500494	GGGGAACAGCCTTGC[A/G]GGGGGCCTCTCATTC	90678
rs376452859	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127468188	GAAGTTTGACAGAGA[A/G]AGGGCCAGTGTAGCT	90678
rs376468970	snp	C/T	0.000173411	0.00930997	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127489501	AAAGACCTGATGCAT[C/T]GGCAGATCAGGAGCC	90678
rs376478532	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127475037	CTGCTGCTGGGAATG[C/T]ATTTGGGATTTTATT	90678
rs376509064	snp	C/G	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127503070	GCATGTCTGGGCCAG[C/G]CAGAGGTGCTCCTCA	90678
rs376539448	snp	A/G	0.0023933	0.0345097	intron-variant	LRSAM1	GRCh38.p7	9:127475844	CTCCCGGGTTCAAGT[A/G]ATTCTCCTGCCTCAG	90678
rs376566243	snp	C/T	0.000307953	0.0124049	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127479848	CTGCAGGAGCAGTCC[C/T]GGCTGGAGCAGGGCC	90678
rs376651049	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127493897	TGCCCTCTGAGCTGC[A/G]TCCTAGGCCGGGTCC	90678
rs376653112	snp	A/G	4.94637e-05	0.00497287	intron-variant	LRSAM1	GRCh38.p7	9:127473751	CGGGTGTCTCTGGGT[A/G]CCTCAGCTGTCTCCT	90678
rs376668273	in-del	-/CAG			intron-variant	LRSAM1	GRCh38.p7	9:127498378	TCTCAGACTGGAGAT[-/CAG]AAGAGTTTTCCATCA	90678
rs376671005	snp	C/G/T	9.88393e-05	0.00702929	missense, synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127473865	GGAGCAAGATGGAAT[C/G/T]GAGAACTCTCGGGAC	90678
rs376788441	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127487143	GAGCCACGATCACAC[C/T]ACTGCACTCCAGCCC	90678
rs376813315	snp	A/G	0.000133109	0.00815702	intron-variant	LRSAM1	GRCh38.p7	9:127481158	TGCTGGTGACTGCCA[A/G]GACCTTTTATGATTT	90678
rs376815374	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127457262	CCACGCCCTTAGCCT[C/G]CCCTGCCTGCTGCTC	90678
rs376818096	snp	A/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127489165	ATGCCTCTGAGTGTC[A/T]CTCCCCATCTGTGAA	90678
rs376895221	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127475991	GTGATCTGCCCACCT[C/T]GGCCTCCCAAAGTGC	90678
rs376907092	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127458769	GGCATACTGTTTTAT[A/G]GCATAGTTTTTCAGT	90678
rs376913816	snp	C/T	1.65299e-05	0.00287483	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127501061	CGGCCCCCCAGGAGC[C/T]TCCTGAGTCTGTGAG	90678
rs376964930	snp	G/T			intron-variant	LRSAM1	GRCh38.p7	9:127473313	AACATATTATAGACC[G/T]AAGGTTATTAACTAC	90678
rs376995440	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127502450	AGCACTTTGGGAGGC[C/T]GAGGCGGGCAGATCA	90678
rs377012683	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127455350	CACAATGGGGACAGG[C/G]TGGGTGGGGCAGGGC	90678
rs377045300	in-del	-/CCCC			frameshift-variant, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127496043	CATCTTTGCGCACCA[-/CCCC]CCGCCTCTCACTGGA	90678
rs377079293	snp	C/T	8.35038e-05	0.00646103	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127482970	GAATGGAACAGTTGA[C/T]GTCCATAACCCAGGA	90678
rs377144291	snp	C/T	1.65353e-05	0.00287531	intron-variant	LRSAM1	GRCh38.p7	9:127485729	TCCCCACCTCATGTT[C/T]CCACAGCCGCCATGC	90678
rs377190920	snp	C/G/T	0.000209968	0.0102444	intron-variant	LRSAM1	GRCh38.p7	9:127492797	GGGTGTGGTCTTGTT[C/G/T]GCAGGAGATGATCTC	90678
rs377202765	snp	A/C/G			intron-variant	LRSAM1	GRCh38.p7	9:127490191	TGGGAGTACTCCTGC[A/C/G]TCATGTTCAGCACAC	90678
rs377206145	snp	A/G	5.14161e-05	0.00507005	intron-variant	LRSAM1	GRCh38.p7	9:127479818	GTCCCAGGGGCTCAG[A/G]ACCCCTACCTCCGGC	90678
rs377382271	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127461100	ACCTTGTGATCCACC[C/T]GCCTCGGCCTCCCAA	90678
rs377449253	snp	A/C			intron-variant	LRSAM1	GRCh38.p7	9:127469632	ATGGAAAAAAAAAAA[A/C]AAAAAACTTCCTGCT	90678
rs377458654	snp	C/T	1.76089e-05	0.00296718	intron-variant	LRSAM1	GRCh38.p7	9:127502744	GGAACCCGGTAGGGC[C/T]AGCCACATGCTCCCG	90678
rs377491843	snp	A/G	1.67097e-05	0.00289043	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127501126	GCCTCAGAGTGTGTC[A/G]TGTGCCTGGAACGGG	90678
rs377514836	snp	C/T	0.000478425	0.0154591	intron-variant	LRSAM1	GRCh38.p7	9:127461145	AGGCATAAGCCACTG[C/T]GCCTGGCTGCCTCTT	90678
rs377678883	snp	A/G	0.000118695	0.00770283	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127496038	CCTGCCCATCTTTGC[A/G]CACCACCGCCTCTCA	90678
rs377684556	snp	C/G			upstream-variant-2KB, intron-variant, utr-variant-5-prime	RPL12, LRSAM1	GRCh38.p7	9:127452264	CTGCACATCAGGAAG[C/G]GGGTGCAAGAGGGTT	90678
rs377685232	snp	A/G	0.00199481	0.0315187	intron-variant	LRSAM1	GRCh38.p7	9:127489876	GGAAAAGCAGCCGGC[A/G]CAGGCCCCAGCGCTC	90678
rs377724752	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127463850	AACCTGGAATCGCTC[C/T]GTGTATCGTCACAGA	90678
rs386416258	in-del	-/G			upstream-variant-2KB, intron-variant	RPL12, LRSAM1	GRCh38.p7	9:127452326	CATCAGGGACGGATG[-/G]GGGGAGGGCTGTTTT	90678
rs386738658	multinucleotide-polymorphism	CC/GG			intron-variant	LRSAM1	GRCh38.p7	9:127474309	GTCTTGCTCCATCAC[CC/GG]AGGCTGGAGTGCAGT	90678
rs387907032	snp	A/C/G	1.65438e-05	0.00287605	LRSAM1	9	allele_origin=G(germline)/A(germline)	9:127501011	TCTGGTCCCCACAGA[A/C/G]CTGAAACCACCAATG	90678
rs397737639	in-del	-/A			intron-variant	LRSAM1	GRCh38.p7	9:127469631	ATGGAAAAAAAAAAA[-/A]CAAAAAACTTCCTGC	90678
rs397773513	in-del	-/CA			intron-variant	LRSAM1	GRCh38.p7	9:127479097	TTCCTCTTACACGCA[-/CA]GTCTGCTGCATCCTC	90678
rs527250569	snp	A/G	0.0236746	0.106192	intron-variant	LRSAM1	GRCh38.p7	9:127472313	TATATATATATATAT[A/G]TGTGTGTGTAAAATT	90678
rs527361646	snp	C/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127465727	TCAGAGCTTCCCAGG[C/G]CTTCTCCTTTTCCAG	90678
rs527431394	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RPL12, LRSAM1	GRCh38.p7	9:127453396	GTGTTTCTTCACTTT[A/T]AAAAGGGTTATGGTG	90678
rs527436982	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127498088	GCTGCTGGGCTGGGC[A/G]AGGCTCTGGACAGGG	90678
rs527462088	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127498794	CCAGGTGTGGTGGCT[C/T]ACACCTGTAATCCCA	90678
rs527534670	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127493405	AAACATTGTGATGCA[C/T]CTTTATAGCTGTTCG	90678
rs527535011	snp	C/T	8.3999e-05	0.00648016	intron-variant	LRSAM1	GRCh38.p7	9:127485855	GGTAAGGAAGAGGAG[C/T]CCCAGGTGAGGGAGC	90678
rs527638000	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451092	CACAGGTGGTCCAGT[C/T]CTCCCTCCCCACCTA	90678
rs527664170	snp	G/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127497142	GAAGGCTTCCACATT[G/T]CCAGCAGGAGGTGTC	90678
rs527668507	snp	A/G	0.00076297	0.0195167	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127502867	TGCCGCCAGGACATC[A/G]CCCAGCGCCTCCGCA	90678
rs527739103	snp	C/T	0.000100717	0.00709565	intron-variant	LRSAM1	GRCh38.p7	9:127491299	GAGTCACTCCAGGTA[C/T]GTAGGGCTCCCTGCC	90678
rs527770831	in-del	-/T			intron-variant	LRSAM1	GRCh38.p7	9:127484529	ACCTCACCTGGCTAA[-/T]TTTTTTTTTTTTTTG	90678
rs527773567	snp	A/G	0.000798403	0.0199641	utr-variant-5-prime, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451379	AGGAAGTTGCACCTT[A/G]GCCTCCTCCGAGCCG	90678
rs527922318	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127484818	TTTTTTTCTTTTTTT[C/T]TTTTTTTTGAGATAG	90678
rs527942458	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127471089	ATAGCCACCAGGCCA[C/T]ACATATGCAAATTAG	90678
rs527961428	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127478059	CTCCGTCTCAAAAAA[A/G]AAAAAAAAAAAGAAG	90678
rs527980312	snp	C/T	0.00953873	0.0683987	intron-variant	LRSAM1	GRCh38.p7	9:127464445	CCAGAGCGGCAGCCG[C/T]TGGCCATATGTATCT	90678
rs528068464	snp	G/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127494414	CCCCACCCTGGGCAG[G/T]TTACTCATCACCCTG	90678
rs528107581	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127495123	TGCCTGGCTAGTTTT[A/G]TATTTTTAGTAGAGG	90678
rs528107662	snp	A/G	6.00715e-05	0.00548016	intron-variant	LRSAM1	GRCh38.p7	9:127487774	AGGAGGTGAGCCCTC[A/G]CCCAGAGCCTGAGGG	90678
rs528255972	in-del	-/A	0.00159617	0.0282053	intron-variant	LRSAM1	GRCh38.p7	9:127483562	CATTAGCATGTTATC[-/A]GGGGGAGTGTTCATA	90678
rs528279848	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127480787	CCTTCTCCCAGGTTC[A/G]AGCAATTCTCTTGCC	90678
rs528285378	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127497778	CAGGTCGTGAGGCCC[A/G]TGGGGAGAAGGGGCA	90678
rs528316559	snp	G/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127474603	CATGTCTGTCTCCCC[G/T]GCTGGATGAAGCTTT	90678
rs528323200	snp	A/G	0.00199481	0.0315187	intron-variant	LRSAM1	GRCh38.p7	9:127481423	ACCAGCTAATTTTTT[A/G]TATTTTAGTAGAGAC	90678
rs528338329	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127475232	AAGAAGAAAACCATC[A/G]CAATAGAAAAAATAT	90678
rs528343584	in-del	-/TTTAC	0.0146602	0.0843514	intron-variant	LRSAM1	GRCh38.p7	9:127475077	TTATTATTATTTTAT[-/TTTAC]AGTTCAGCAAGAATT	90678
rs528352786	snp	A/G	0.00279162	0.0372561	intron-variant	LRSAM1	GRCh38.p7	9:127458191	TTCAAGACCAGCCTG[A/G]CCAACATGGTGAAAC	90678
rs528353185	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127486591	ATGTGGGAATTTCTC[C/T]CCCCTTTCCTGATAT	90678
rs528381613	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127469193	ACACAAGAGAATATC[C/T]ACACGGTGGCTCACA	90678
rs528454544	snp	C/T			utr-variant-3-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127503098	TCATCCATGACACCA[C/T]CAGTCTGAATGGTCC	90678
rs528463549	snp	A/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127478804	TCCCCCGACCCCACC[A/T]TTCTGAGGCAGTGGT	90678
rs528549251	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127472944	GTGAGAGGGCACGAG[C/T]GCCCTAGGGTGCCTG	90678
rs528559853	snp	A/C			intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127450251	AATGAAATTCAGAGA[A/C]ATCCAAGAGGACAGA	90678
rs528577487	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127473669	TGAAAAACACGAAGC[A/G]CCCAGGCTAGGGAAG	90678
rs528654207	snp	A/C			upstream-variant-2KB, intron-variant	RPL12, LRSAM1	GRCh38.p7	9:127452597	CTAACATTTATTGAG[A/C]GCTCATGTGCCAGGT	90678
rs528797347	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127454788	CCCCTGTAGACTGAG[C/T]GCACTGTCATTGCTT	90678
rs528824237	snp	A/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127500099	GGCACGTTGGCTCAC[A/G]CCTGTAATCCCAGCG	90678
rs528848096	snp	A/G	0.000399281	0.0141238	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127482994	CCCAGGAGGAGACTG[A/G]GAGCCTGCGGCGACG	90678
rs528909104	snp	C/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127476438	CTGTGGTCCCAGCTA[C/G]GAGGGAGGCTAAGGT	90678
rs528954004	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127470370	CTTATAAAACCATCA[A/G]ATCTTGTGAGAACTC	90678
rs528995146	snp	A/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127470879	AGATTCTGTGCTCTC[A/G]GCCCAAAGGCAGTGA	90678
rs529020697	snp	C/G	0.000399281	0.0141238	downstream-variant-500B	LRSAM1	GRCh38.p7	9:127503657	CAGGTAGGGCCATCT[C/G]GAATGTCGTGTTATC	90678
rs529190351	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127458306	AGAATGGCGTGAACC[C/T]GGGAAGCGGAGCTTG	90678
rs529197347	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451389	ACCTTGGCCTCCTCC[A/G]AGCCGAAAGCCGAGA	90678
rs529297543	snp	A/C	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127461841	TGTCCTTAAGCACTT[A/C]CTGCAGAGTGCCTCT	90678
rs529319339	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127465603	GGGGCAGTCTCCCAC[C/T]CCCTGTGCAAAGCAC	90678
rs529320034	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451185	GGTCTCTGGGAGGCA[A/G]CGGCTTTAAGAGCCC	90678
rs529333601	snp	A/G	0.000263552	0.0114764	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127462359	CAGATGCTGGCTCAC[A/G]TTCGAACCCTGGAGG	90678
rs529406140	snp	A/G	0.0023933	0.0345097	intron-variant	LRSAM1	GRCh38.p7	9:127502567	TGGTGCACGCCTGTA[A/G]TCCCAGCTACTTGGG	90678
rs529427403	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127450434	CGAGGAAATACAGAT[G/T]TTGGCTGCCCAATGT	90678
rs529495161	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127490357	GCTCATTCCTCTGAC[C/T]AGGGGTTGGTGGTGT	90678
rs529499051	snp	C/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127482525	CATTCTGCCAGTTTA[C/G]ACTCCTCTCAGCAGT	90678
rs529687559	snp	C/T	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127459576	CTTTTTGTATGTGTA[C/T]TTTTTTTTTCTCACT	90678
rs529824791	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127471743	AGTGAGCTGAGATCT[C/T]GCCACTGCACTCCAG	90678
rs529837418	snp	C/T	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127499567	ATATATGAATGCCCC[C/T]TCGAAATGGTGGTTT	90678
rs529843132	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127488514	TGATCCACCCACCTC[A/G]GCCTCCCAAAGTGCT	90678
rs529892969	snp	A/G	0.00199481	0.0315187	intron-variant	LRSAM1	GRCh38.p7	9:127487373	CCACCCATGGAGGTG[A/G]CTGGGCAGAGGCAGG	90678
rs529932984	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127490038	TCCTCTTAGACCCTC[C/T]CTCATGTGACAAGAT	90678
rs529995344	snp	C/T	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127483560	CCCATTAGCATGTTA[C/T]CAGGGGGAGTGTTCA	90678
rs530064716	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant, splice-donor-variant	RPL12, LRSAM1	GRCh38.p7	9:127452300	TTGGGGAGCAGAAGG[C/G]TAAGTGCTGGTCATC	90678
rs530082224	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127497886	CGTTGAGGAACCTCC[A/G]GATCCATCCCGTGAG	90678
rs530124114	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127481628	CTAAAGCTATAAGGA[A/G]ATTCACCTCCTTAGA	90678
rs530125989	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127491968	GTGTGAGGACATGTG[C/T]CTGTGCCAGGAGTTT	90678
rs530170232	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127484900	GCAACCTCTGCCTCC[C/T]GGGTTCAAGCGATTC	90678
rs530264574	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127471859	GTAAAGACAGGGTTT[C/T]GCCATGTTGACCAGG	90678
rs530301480	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127465196	CATGGCCAGCATGCA[A/G]TGAGCCGGGATCTGA	90678
rs530309442	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127478157	CCAATAATTACATTA[C/T]ATTATTGATGTTTAA	90678
rs530347856	snp	A/C	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127478747	TCTCATCAGGTGTCC[A/C]CTGGAACCACCTGGT	90678
rs530580017	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127487324	AGCTTTGTCATACTT[C/T]GGTGGCTCACCACCC	90678
rs530748340	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127484635	GTAAGTGCTTATATT[A/G]CAGGTGAGCCGCCAT	90678
rs530762565	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127460823	CTGTGTGTGGGTTCT[C/G]GTGTCACCTCTTCCT	90678
rs530777056	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127469226	TGTAATCCCAGCACT[C/T]TGGGAGGCTGAGGTG	90678
rs530804896	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127473095	GAGAGCCCATTATTA[C/T]TCTAATGTCACTTCC	90678
rs530807508	snp	C/T	4.99563e-05	0.00499756	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127479886	GCACCAGCGCCACCT[C/T]AACGCAGAGCGGCAG	90678
rs530814374	snp	A/C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127461933	ACAGCATGAGGGGCC[A/C/T]TGTGCGGAGGACCTC	90678
rs530897533	snp	C/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127478629	CAGATATCCCATTTC[C/G]TGCTCTGCTCTTCAG	90678
rs530966547	snp	C/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127473736	CCCTGGCAGTGGGAG[C/G]GGGTGTCTCTGGGTA	90678
rs531034044	snp	C/T	0.0490535	0.14873	intron-variant	LRSAM1	GRCh38.p7	9:127460872	TTTTTTTTTTTTTTT[C/T]TGAGACGGAGTCTCA	90678
rs531158843	snp	A/T			intron-variant	LRSAM1	GRCh38.p7	9:127468342	AAGAAAGAGTGCAGG[A/T]CAGGGGACCAGTTAG	90678
rs531212208	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127455463	TGCCACCTGCTGTGG[C/T]GTTTTGCCCTTGTTC	90678
rs531487638	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127458690	CTGTCAATATTTTAT[C/T]GCATATTTGAAAGTC	90678
rs531488547	snp	C/G	0.000798403	0.0199641	utr-variant-5-prime, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451407	CCGAAAGCCGAGAGG[C/G]CGGAAATCGCGCGGA	90678
rs531614801	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127472207	CCTCGTGATCCACCC[A/G]CCTCAGCCTCCCAAA	90678
rs531629296	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RPL12, LRSAM1	GRCh38.p7	9:127452432	CCCAGACAGCCCCGC[C/G]CCCGTGGGTGCAGAG	90678
rs531640717	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127457246	GGCGCTGGGCTGGCT[C/T]CCACGCCCTTAGCCT	90678
rs531712362	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127450928	CACAGAGCGCGAGGC[A/G]GGCCACCCGCTCCTC	90678
rs531757516	snp	A/C	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127496652	ATCTTTCAGTTGAGA[A/C]CCAGTAAGGCAATAA	90678
rs531761618	snp	A/C	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127503438	GCTCTCCACAACTGT[A/C]CCTCCTTACCCCATG	90678
rs531794021	snp	A/G	0.00795532	0.062565	intron-variant	LRSAM1	GRCh38.p7	9:127495153	GTGGGGGGTTTCTCC[A/G]TGTTGGTCAGGCTGG	90678
rs531845026	snp	A/C	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127483086	GGCAGGGTGGATGGC[A/C]CTCCCTCTGTTGGCC	90678
rs531854617	snp	A/C	0.00199481	0.0315187	intron-variant	LRSAM1	GRCh38.p7	9:127476577	AAAGAAAACTCAAAA[A/C]AAAAAAAGGAAACAG	90678
rs531890652	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127477191	TGGGCCTGATAATGA[C/T]AGTTACACCTGACAG	90678
rs531936817	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	LRSAM1	GRCh38.p7	9:127454165	CACTAGAAAGACGCA[A/G]CCCCTGCCTCCGTGA	90678
rs531943553	in-del	-/T			intron-variant	LRSAM1	GRCh38.p7	9:127474262	TTATCCTTCAGTTCT[-/T]TTTTTTTTTTTTTTC	90678
rs532071633	snp	C/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127486792	ATGAGTGTTGATGAG[C/G]ATAATCTCTAGTGCA	90678
rs532101926	snp	G/T			intron-variant	LRSAM1	GRCh38.p7	9:127490538	ATGGTTTTGACCAGG[G/T]CAGCTATTGCCCTTA	90678
rs532128661	snp	C/T	0.00557542	0.0525036	intron-variant	LRSAM1	GRCh38.p7	9:127499652	ATCTTTAGTTGTGGC[C/T]GGGTGCGGTGCCTCA	90678
rs532165357	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127499986	CTTGTAATTCAAGCC[A/G]TAGAATAAAGTGAAC	90678
rs532247323	snp	C/T	1.64741e-05	0.00286998	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127473880	CGAGAACTCTCGGGA[C/T]AGCCCTGATGGGCCC	90678
rs532278475	snp	A/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127480739	GTCACTGAGGCTGGA[A/G]TGCAGTGGTGTGCTC	90678
rs532284063	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127474495	CGAGGTCAGGTCTCC[C/T]GTTGTGTGTTCTCAG	90678
rs532341280	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127460069	CAGTGGTGTGATCTC[A/G]GCTCACTGCAATCTC	90678
rs532371463	snp	G/T	5.15389e-05	0.0050761	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127479898	CCTCAACGCAGAGCG[G/T]CAGCGGCTGCAGGAG	90678
rs532520697	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127458981	TCTCACTTGGAGACT[C/T]ACAGGGGTCTTTCTT	90678
rs532532023	snp	C/T	9.98193e-05	0.00706397	intron-variant	LRSAM1	GRCh38.p7	9:127492768	CTGCGCTGCCGCCAG[C/T]TCACGGTGGTGCGGG	90678
rs532571644	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127485619	CTATCAGGTAGGTAA[C/T]CAGGTGAGGCCTCAA	90678
rs532586450	snp	A/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127478364	GATGATGTTTTTGCA[A/G]AAGTAGAATCATGCT	90678
rs532661718	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127472351	TGACCTTTTAAAAAA[C/T]ATTAAAGAGGCTGGG	90678
rs532673197	snp	C/T	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127459710	ATTACAGGCACACGC[C/T]ACCACACCTGGACAA	90678
rs532763743	snp	A/G	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127489692	TCCCAGCCTTGTGTC[A/G]GGGCTGCTGGGAGGG	90678
rs532820610	snp	C/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127466471	TATCTAACAAAGGAA[C/G]AATCATATATATATA	90678
rs532862339	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127475868	GCCTCAGCCTCCCGA[A/G]TAGCTGGGATTACAG	90678
rs532993031	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127475326	TAAAACCCTGTCTCT[A/G]CTGAAAATGCAAAAC	90678
rs533062691	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127469838	GGCGTGGTGGCGGGC[A/G]CCTGTAGTCCCAGCT	90678
rs533089100	snp	A/G	0.00159617	0.0282053	intron-variant	LRSAM1	GRCh38.p7	9:127457762	CTCCTCCCCGGATGG[A/G]CTGGGAGGCATTCAC	90678
rs533117217	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	LRSAM1	GRCh38.p7	9:127503619	AGCCAGGAGTGCGCC[A/G]CACCTCAGTCGAGAG	90678
rs533193448	snp	A/C	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127467901	ACCCTGTGCCAGCCC[A/C]GGCTGGGGAACAGCA	90678
rs533193770	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127462626	ATCCAGAAGAGGCTG[A/G]CACTTTAAGAAAGTT	90678
rs533202276	snp	G/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127470231	TCTTTATAAAGAAAA[G/T]AAGTTTAATTGACTC	90678
rs533231306	snp	A/C/T	4.9603e-05	0.00497991	missense, synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127457339	CGTCCACACGAATCA[A/C/T]CTCACTTCCCTGCTT	90678
rs533243061	snp	A/C	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127463341	TGCTGAGCTTGTGTG[A/C]TATGGGGCCCAGAAA	90678
rs533320263	snp	C/T	0.00755907	0.0610114	intron-variant	LRSAM1	GRCh38.p7	9:127456426	TTTAGAGATGAGGTT[C/T]TGCCATGTTGGCCAG	90678
rs533371432	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127495700	TCTGTCCAGCACCTG[C/T]GGGGACAGAGAGGCA	90678
rs533386352	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127497041	ACCCCTGCCACACTG[A/G]TTGTTGGGCTGAGGC	90678
rs533484572	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127455502	CCTGTCTCTTCCTCA[C/T]GTGAATGCCACTCAG	90678
rs533530081	snp	G/T			intron-variant	LRSAM1	GRCh38.p7	9:127499095	AACAAATATAGAAGC[G/T]GGGTGCAGTGGCTCA	90678
rs533548560	snp	C/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127490994	CAATTTTGGCCACAA[C/G]AAGCACGTCCATGCC	90678
rs533660381	snp	C/T	6.84955e-05	0.00585176	intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127449587	CCCACCCTCCTCTCC[C/T]GAAACCAAGCACAAG	90678
rs533724746	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127484585	GGCTGGTCTCAAACT[C/T]CTGGGCTCAAGCAGT	90678
rs533783786	snp	A/C	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127497691	CAGGGCCTGCAGTAT[A/C]CCCAATGCTGGGCCT	90678
rs533784001	in-del	-/CCCTGCCTCATGGTGTCACAAACTGTC	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127496395	CTGATCCAGCCTCTG[-/CCCTGCCTCATGGTGTCACAAACTGTC]GTGGCCACAGCACTG	90678
rs533801322	in-del	-/CTTT			intron-variant	LRSAM1	GRCh38.p7	9:127490274	TTTCTTTCTTTCTTT[-/CTTT]TTTTGGACCAATTTA	90678
rs533863891	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451476	AACTGTCGTCACTGC[C/T]CGGCCTTCCAGAGAC	90678
rs533950773	snp	A/C			intron-variant	LRSAM1	GRCh38.p7	9:127472249	ACAGGCGTGAGACAC[A/C]ACGCCTGGCCAAGAA	90678
rs533953015	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127482737	CATTTTCTAAGGGAG[C/T]GTCCATCTTTTTACA	90678
rs533989085	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127476179	ATTGGATGCCCCCCA[A/G]ATGTTTGTCAGTGAG	90678
rs534039871	snp	C/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127471393	GGAGGATTGCTTGAG[C/G]CTAAGAAGTGGAGGT	90678
rs534113795	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127497688	CCCCAGGGCCTGCAG[C/T]ATACCCAATGCTGGG	90678
rs534136801	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127461483	CAGGGCCGTATGGCC[A/G]TATGGGGAGGAGGGC	90678
rs534160824	snp	A/G	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127463058	AGAAATTATCCAGGC[A/G]TGGTGGTGCGCACCT	90678
rs534175399	snp	A/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127481989	TAAATTTCTGGAAAG[A/G]AAAATTATTTAGTTA	90678
rs534196643	snp	A/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127463872	CGTCACAGAACTCTT[A/G]TGAGGCAGATACTAT	90678
rs534250089	snp	A/G	0.00199481	0.0315187	downstream-variant-500B	LRSAM1	GRCh38.p7	9:127503756	TGTGCCTCCATGAGC[A/G]GAGGAGCCCTGTGTG	90678
rs534301130	snp	A/G	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127479062	TCTTCCCAGCTCAGA[A/G]TTAGAGGTCACAGTA	90678
rs534373076	snp	G/T	1.65534e-05	0.00287688	intron-variant	LRSAM1	GRCh38.p7	9:127480023	AGAGTCCTTCCCCGT[G/T]CAGTCCCCTGAGGAG	90678
rs534392052	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127476667	AATTTTCGAGGGTGA[C/T]GGAATTGTTTTCTTT	90678
rs534468825	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127481928	GGAGTGGTGGCAGGC[A/G]CCTATGGTTCCAGCT	90678
rs534476658	snp	G/T			intron-variant	LRSAM1	GRCh38.p7	9:127478267	CGTTGCCTGGAGGTA[G/T]TCATCATTAACTGAT	90678
rs534506320	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127467026	AAAGTGCTTGCTGCT[A/G]TTGTAACCAAGCGAG	90678
rs534541005	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127460497	GGGGAACTAGAGCCT[C/T]CTGTGCTGCCTCCCC	90678
rs534541360	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127467655	GGGTAGAGGTGACAG[A/G]GAACACACAAATTGA	90678
rs534577500	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127460916	GCCGGAGTGCAATGG[C/T]GCAATCTCAGCTCAC	90678
rs534613407	snp	A/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127461376	AGCCAGTCTCCGGGG[A/G]TCGCTGTAAATGGAC	90678
rs534629574	snp	A/C	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127479659	GGCCCTTACAGATCA[A/C]CCAGCCCAGCCTCCC	90678
rs534666587	snp	A/G	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127473359	CCTACAAATCAACAG[A/G]AAAAAGACAAACAGC	90678
rs534783295	snp	C/G	1.69542e-05	0.0029115	intron-variant	LRSAM1	GRCh38.p7	9:127459118	ATGGCCTTAGTGAGA[C/G]CAGGCAGTCACTCAA	90678
rs534828834	in-del	-/TT	0.00199481	0.0315187	intron-variant	LRSAM1	GRCh38.p7	9:127499128	GCTGTAATCCCACAC[-/TT]TGGGAGGCCTACGTG	90678
rs534834402	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127498511	GCAGTCCTCAGGACC[A/G]GCTGCTTCTCACTGT	90678
rs534992818	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	LRSAM1	GRCh38.p7	9:127454336	CTAGAAAGACCCAGC[C/T]GCTGCCTCCGTGGAA	90678
rs535038018	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127471074	GGGGTGGCTGCGATC[A/G]TAGCCACCAGGCCAC	90678
rs535053727	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127465277	CCCACGATGAGAATG[C/T]TCTATGATCTGTGCA	90678
rs535135359	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127459784	GGCTGACCTCAAACT[C/T]CTGGCCTCAGGTGAT	90678
rs535144476	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127500565	CTCCTGGGCAACCAG[A/G]TGGAGAAGCCAAGAG	90678
rs535181174	in-del	-/T	0.00279162	0.0372561	intron-variant	LRSAM1	GRCh38.p7	9:127487052	AGCCAAACGTAGCAG[-/T]GGGCGCCTGTAATCC	90678
rs535183475	snp	G/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127499170	TCAAGCCCAGGAGTT[G/T]GAGACCAGCCTGGGC	90678
rs535236201	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127493138	GCAATCTCAGCTCAC[C/T]GCAGCCTTGACTTCC	90678
rs535243852	snp	A/G	0.000221361	0.0105182	utr-variant-3-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127502940	TCCTAGCCCTGCCTC[A/G]GCCACTGTGAGCCCC	90678
rs535270189	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	LRSAM1	GRCh38.p7	9:127453698	GCCTCACTATGGGTC[A/G]GTGGCAAATATGGGC	90678
rs535383474	snp	C/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127493710	AGGAGTGGCCCAGCT[C/G]TCCCTGTCCCCTGAT	90678
rs535442757	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127502408	ATAATGAAGGGGGCC[A/G]GCATGGTGGCTCACG	90678
rs535461396	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127488030	CCTGTGTAGGAGGCT[C/T]CATTGGAAGGACTTA	90678
rs535473292	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127469700	CGGGCGCGGTGGCTC[A/G]CGCCTGTAATCCCAG	90678
rs535476934	snp	C/G	0.000399281	0.0141238	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127462275	CTGAAGGAGCTTCCA[C/G]ACACCGTGGGGGAGC	90678
rs535511291	snp	A/G	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127456882	AAAAAAAAAAAAAAG[A/G]AAAGGAAAAATAGCA	90678
rs535513300	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127462771	GTGCAGCAAACCACC[A/G]TGGCACATGTTTACC	90678
rs535593496	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127488908	TCTTTCCTGCAGCCC[C/T]GTGGGAGTCTTGCCG	90678
rs535628749	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127476041	CACCACACCCGCCAG[A/G]TGTCAAAAATTTTCA	90678
rs535634164	snp	A/G	9.98469e-05	0.00706495	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127481202	AAGAAAAGCTCCGAG[A/G]TTTTGAAATCGCTGG	90678
rs535634291	snp	A/G	0.000702076	0.0187229	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127489449	TGTGTTGCAGAGCGC[A/G]ATGCAGAAGGCTGCG	90678
rs535667952	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127490074	CCACCCCCCGCAGGC[C/T]GGCTGCTGACCTTCA	90678
rs535668622	snp	A/G	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127481849	TCACTTGAGGTCAGG[A/G]GTTTGAGACCATCCT	90678
rs535790080	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127490653	TCAGTTTTCTTGTCT[A/G]TAAAATGGAGGCAAT	90678
rs535790217	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127482812	GGGTTGCTTGTGATG[C/T]GGTAGGCATCCAGAG	90678
rs535854208	snp	A/G	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127491829	GGACTGGATGCCTGG[A/G]AGCCGGGTGTGGCCC	90678
rs535929129	in-del	-/T	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127460264	AGCCTCCCAAAGTGC[-/T]TGGGATTACAGGTGT	90678
rs536034722	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127485901	AGGGCCCAAGACCGT[A/G]GGATGAGAGCTGGGC	90678
rs536074997	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127478860	CATCAGGCCACCCGG[A/G]GGTTCCTGGTGCCCA	90678
rs536087985	snp	G/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127472096	CCTCCTGAGTAGCTG[G/T]GATTACAGGCGCCCA	90678
rs536230347	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127498272	TCCAGGGACACTGAC[C/T]CAACCCCCAAAAAGT	90678
rs536238555	snp	A/C			intron-variant	LRSAM1	GRCh38.p7	9:127457148	TTAAGGAAGGGCATT[A/C]GATTCCCCATTGGGA	90678
rs536246220	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127485004	GTACAGACACAGTTT[C/T]GCCATGTTGGCCAGG	90678
rs536269725	snp	C/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127476793	AATTCTCCTGCCTTA[C/G]CCTCCCGAGTAGCTG	90678
rs536337780	in-del	-/ATC	0.00159617	0.0282053	intron-variant	LRSAM1	GRCh38.p7	9:127495808	TGGGCCTATCTATCT[-/ATC]ATCTATCTCTGTGTG	90678
rs536378920	snp	A/G	0.00676609	0.0577691	intron-variant	LRSAM1	GRCh38.p7	9:127462793	ATGTTTACCTTTGTA[A/G]CAAACCTGCACGTGC	90678
rs536442147	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127464030	ACCTCTGTATGACTC[A/G]GCTTCTGGAACAGGG	90678
rs536480093	snp	C/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127464493	TGGCTTGTGTGTACA[C/G]CCAGGAACTAAAAGT	90678
rs536516149	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127472510	GCTGGGTGTAGTGGC[A/G]CATGCCTATAATCCC	90678
rs536752308	snp	C/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127468366	CAGTTAGGAGGCTGT[C/G]GGGGTCATCCAGGAG	90678
rs536790131	snp	A/G	0.00159617	0.0282053	intron-variant	LRSAM1	GRCh38.p7	9:127502506	CCTGACCAACATGGT[A/G]AAACCCCATCTCTAC	90678
rs536830480	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127481500	TGATCTGCCCGCCTC[A/G]GCCTCACAAAGTACT	90678
rs536847582	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127471249	TTTGGGAGGCCAAGG[C/T]GGGTGGATCGCTTGA	90678
rs537013130	snp	A/G			missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127479479	AGCAGCAGCCAGAAG[A/G]ATGAGATCCTTCAGA	90678
rs537060702	snp	A/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127499270	TTCCAGCTACTCGGG[A/G]GGCAAAGGTGGGAGG	90678
rs537075932	snp	C/G	0.00199481	0.0315187	intron-variant	LRSAM1	GRCh38.p7	9:127474044	GAGCTGCAGCTCCCA[C/G]ATTCCTCCATAGAAC	90678
rs537081121	snp	G/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127466870	AAATTAGGCATGGTG[G/T]CATGTGCTTATAGTC	90678
rs537198253	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127499746	CCATCCTGGCTAACA[C/T]GGTGAAACCCTGTCT	90678
rs537250384	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127501226	AGGGTTGTCTCTGAA[C/T]GTGTTTTCTCCAGTT	90678
rs537302373	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127487842	GTGCAGAGCTCCACA[C/T]GGAGCCCTTCCTAGA	90678
rs537401439	snp	A/G	1.6528e-05	0.00287467	missense, intron-variant, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127495329	TGGCAGACGGAGTTA[A/G]AAGCCAAAAGTGAAA	90678
rs537420010	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127503038	CACTGCCCAGGAGCC[C/T]CCATCCTAAGCTCCA	90678
rs537454638	snp	A/C	0.000399281	0.0141238	downstream-variant-500B	LRSAM1	GRCh38.p7	9:127503739	CGGTGATGGCTGCGG[A/C]CTGTGCCTCCATGAG	90678
rs537458439	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127496846	CAGGCTCTGGAGGCT[A/G]AGGGACTGTGGGGCT	90678
rs537511807	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127460386	AGGGAGCACAGCTTC[A/G]GAATCCAACAAGCCC	90678
rs537550075	snp	C/T	0.00119737	0.0244387	intron-variant, utr-variant-5-prime	LRSAM1	GRCh38.p7	9:127454370	ACTAGGGAGACACAG[C/T]CCCTGCCTCCATGGA	90678
rs537598396	snp	C/T	1.67047e-05	0.00288999	intron-variant	LRSAM1	GRCh38.p7	9:127497214	CATTTAGCGGGCTCC[C/T]GCCCAGGCCACAGTC	90678
rs537630418	snp	A/G	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127490825	CTGCAACAGCGATGC[A/G]AGGGACAAGAGAACT	90678
rs537634723	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127493867	TCGTTCCTGTGTCCC[C/T]GTGAATGCACCAGAT	90678
rs537666998	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127483449	GAGACCATTTCTCAG[A/G]AAAAAAAAAAAAGAA	90678
rs537671437	snp	A/C	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127487124	GGGAAGTGGAGGTTG[A/C]AGTGAGCCACGATCA	90678
rs537792858	snp	G/T			intron-variant	LRSAM1	GRCh38.p7	9:127484876	TGCAGTGGCATGATC[G/T]CAGCTCACGCAACCT	90678
rs537838691	snp	A/G	0.000134925	0.00821246	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127496046	TCTTTGCGCACCACC[A/G]CCTCTCACTGGACCT	90678
rs537888650	snp	A/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127463765	GAGGCAGCTGCTCAC[A/G]GAAAGCAGCTCTCAC	90678
rs537907506	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127481931	GTGGTGGCAGGCGCC[C/T]ATGGTTCCAGCTAAA	90678
rs538044481	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127489139	GGTGTGTGTCCCAGC[A/G]CCGCTGATTCATGCC	90678
rs538045673	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127475600	TTTCCTTCCTCAAGA[C/T]TGGCACACATTTTGA	90678
rs538067323	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127491632	TCTCTCTCTGTAGGC[C/T]GTGCTTTAGGCCCCC	90678
rs538098333	snp	A/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127476861	TGCATTTTGTTAGTA[A/G]AGACGGGGTTTCACC	90678
rs538123266	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127469926	GCCGAGATTGCGCCA[C/T]TGCACTCCAGCCTGG	90678
rs538224998	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127489024	CTGTTCTAAAATGGT[C/T]TGACTTAGTATCTGT	90678
rs538231072	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127458691	TGTCAATATTTTATC[A/G]CATATTTGAAAGTCT	90678
rs538241441	snp	G/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127485340	AGGCGGGTGGATCAC[G/T]AGGTCAAGAGATCGA	90678
rs538271891	snp	C/T	0.00279162	0.0372561	intron-variant	LRSAM1	GRCh38.p7	9:127486552	GGCGCCTGGACTGTG[C/T]GGGCCTCCCCTGGGT	90678
rs538445367	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127472678	AATAAAAATAAACAT[C/T]AAAGAAACCATAAAA	90678
rs538452546	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127479584	GGGCCAAGGTCCCTC[A/G]GATGTGGAAAGGCAG	90678
rs538460316	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127469691	AAAATAGGCCGGGCG[C/T]GGTGGCTCGCGCCTG	90678
rs538510153	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127466970	CCACTGCACTCCAGT[C/T]TGGGCAATGGGAATG	90678
rs538624550	snp	G/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127493082	TATTTGTTTGTTTGA[G/T]ACAGGGTCTCACTCT	90678
rs538689892	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127479032	TCAACTCATAAAATA[C/T]TTGAGAAAATGACTT	90678
rs538702557	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127483942	GCTGGTATTACAGGC[A/G]TGAGCCACCGTGCCT	90678
rs538927179	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RPL12, LRSAM1	GRCh38.p7	9:127452887	ACAGACACTGTGCAG[G/T]CCCTGGGCAGGCAGT	90678
rs538966226	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	LRSAM1	GRCh38.p7	9:127453571	GACAGCGTTTGGGGG[A/G]CTAGAAGTGATTCAT	90678
rs539010561	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127492531	AAAGGCAGGCACCTG[C/T]GGCTTGTCATTTCTT	90678
rs539062256	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127471294	CATGGGCAACATGGC[A/G]AAACTTCATCTCTAC	90678
rs539101267	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127471922	CCCACCTCGGCCTCC[C/T]GAAGCGCTGGCATTA	90678
rs539126526	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127465221	ATCTGAAGCCATGGC[A/G]GTGTCTTTGGCACAG	90678
rs539160984	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127462174	CCCTAGAGGTCAGAG[C/T]GGCTCCCAGCGGGCA	90678
rs539244065	snp	G/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127498400	GTTTTCCATCAGGAG[G/T]TGGGGTCACCCCCGG	90678
rs539295582	snp	A/C	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127456873	TTGGTCTCAAAAAAA[A/C]AAAAAAAGAAAAGGA	90678
rs539362333	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127450584	ACACGACCTTCCTAA[A/G]GTACCTAGTACTTGT	90678
rs539377408	snp	G/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127485235	TTCAGTGTTTTACAA[G/T]TAGCCTTCCAAGCAT	90678
rs539386709	snp	A/G			downstream-variant-500B	LRSAM1	GRCh38.p7	9:127503731	GCCAGGGCCGGTGAT[A/G]GCTGCGGCCTGTGCC	90678
rs539415527	snp	A/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127499833	GAGAGGCTGAGGCAG[A/G]AGAATCACTTGAATC	90678
rs539417746	in-del	-/C	0.0012141	0.0246085	intron-variant	LRSAM1	GRCh38.p7	9:127501165	CCGGGGCCCTCCCCA[-/C]CCGCCTGCCCTGCCT	90678
rs539447886	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127491852	TGTGGCCCAGCACAG[C/T]CCTGCTGTGCAACTT	90678
rs539465321	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127468409	GAAGGAGCTAAAACC[C/T]GGAGCCAGCACTGGC	90678
rs539551838	snp	A/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127501381	TAAATACATTAGGAA[A/G]AAATTTCCCAAATCA	90678
rs539585295	snp	G/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127494682	GGTGCAGTGGCTCAC[G/T]CCTGTAATCCCAGCA	90678
rs539645674	snp	A/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127496156	CTGTCCTGACCAGCC[A/G]GGGGTTGATCTGCTC	90678
rs539810444	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127490333	CAATTCCACATTGCC[A/G]GACATGAAGCTCATT	90678
rs539859583	snp	G/T	0.000202034	0.0100487	utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127454515	CTAAAGATCGCTCTG[G/T]GAAAAGGGAAGGATG	90678
rs539956426	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127494496	AATTAATGATGGCAT[C/G]GTTAGGTGCACAGCA	90678
rs539994254	snp	A/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127476367	CCTGGGCAATGTGGC[A/G]AGACCCTGTCTCTAC	90678
rs540001114	snp	G/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127487904	TAGAGGTGTACAAGT[G/T]ATCAGGGTGAGGGGT	90678
rs540037457	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127480260	TCCCATCTATAAAGT[A/G]AGTGGGTTTGACAAG	90678
rs540122142	in-del	-/TG	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127449500	CCTCCCCAACAAGGT[-/TG]GAAATCACTCTCGGC	90678
rs540227124	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127486447	GGGGAAAACTCAGTG[C/T]TCAGGAGCCCCAGAC	90678
rs540254230	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127469011	AAAATCAAAATGTCT[C/T]TTCCTCAAAAGATAC	90678
rs540290117	snp	A/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127469772	ATTGAGACCATCCTG[A/G]CTAACACAGTGAAAC	90678
rs540365110	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127483538	TGGCACTCTGCAGTA[C/T]TAGCATCCCATTAGC	90678
rs540406305	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127459321	CCTCCCGAGTTCAAG[C/T]GATTCTCCTGCCTCA	90678
rs540422885	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127502495	TTCGAGACTAGCCTG[A/G]CCAACATGGTGAAAC	90678
rs540455812	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127470819	GCACTGGTTCCTGGT[C/T]ATGAGAGTGTGTTCA	90678
rs540493003	snp	A/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127464350	GGCCATGTGTATCTA[A/T]TGAGCACCTGGTGAC	90678
rs540543461	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127450299	AGTTGCTCAGCAGGC[A/T]TGAGACACAGCCTGC	90678
rs540566362	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127469888	GAGAATGGCGTGAAC[C/G]CGGGAGGAGGAGCTT	90678
rs540622053	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127474859	TTAGCCTGCGTGCCC[C/T]CTCTGCCGCCATCCC	90678
rs540636148	snp	G/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127475688	TGGGAGTGAAAATTG[G/T]TATCACAACTTTGGA	90678
rs540637030	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127501459	TCTTTTGGCCAGGCA[C/T]GGTGGCTCACGCCTG	90678
rs540682355	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127459533	CAATTGTACCACTTT[A/G]AGCCACAATAAATAC	90678
rs540682833	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127461770	GACCACTGCACAGGC[A/G]CCTTACCCGCAGGAG	90678
rs540684561	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127466326	AATAGTAATAATAAT[A/G]GCATTTCATGTAGAT	90678
rs540779407	snp	C/T	0.00199481	0.0315187	intron-variant	LRSAM1	GRCh38.p7	9:127464889	CTCAAGCAATCCTCC[C/T]GCCTTGACTCCCAAG	90678
rs540823744	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127460174	CTGGCTAATTTTTTA[C/T]ATTTTAGTAGAGACG	90678
rs540841189	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127462933	GGGCACCGTGGCTCA[C/T]TCCTGTAATCCCAGC	90678
rs540850298	snp	A/C	0.0023933	0.0345097	intron-variant	LRSAM1	GRCh38.p7	9:127468582	TGGTCTTTTCAATAG[A/C]TGATTCTGGATCAAC	90678
rs540890876	snp	C/T			utr-variant-5-prime, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451385	TTGCACCTTGGCCTC[C/T]TCCGAGCCGAAAGCC	90678
rs540894306	snp	A/C	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127457505	GGGGCCCAATCTACC[A/C]GTCAGTCTGGGATTT	90678
rs540910733	snp	G/T	0.00159617	0.0282053	utr-variant-3-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127503212	CCCAGCTGTCTTGAC[G/T]GAAGGCCACCGCCCC	90678
rs540942030	snp	C/T	0.000150465	0.00867237	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127454536	GGGAAGGATGCCGCT[C/T]TTCTTCCGGAAGCGG	90678
rs540958230	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127499880	CAGTGAGCCGAGATC[A/G]CACCACACTGCACTC	90678
rs540962897	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127490318	TTCCCTCTTTAATTT[C/T]AATTCCACATTGCCG	90678
rs540973158	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127486581	GTCCCTGCAGATGTG[A/G]GAATTTCTCCCCCCT	90678
rs540995312	snp	A/G	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127494169	GAACACAGCCCATCC[A/G]GCTCCTGGGCGCTGG	90678
rs541019846	snp	A/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127497479	GGTTTCCTCCCAAGG[A/G]GCAGGCTTAGGGATC	90678
rs541066469	snp	A/C	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127458214	GGTGAAACCCCGTCT[A/C]TACTAAAAATACAAA	90678
rs541103481	snp	A/G	0.000798403	0.0199641	utr-variant-5-prime, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451380	GGAAGTTGCACCTTG[A/G]CCTCCTCCGAGCCGA	90678
rs541270550	snp	A/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127478068	AAAAAAAAAAAAAAA[A/G]AAGAAGAACCTAACT	90678
rs541300658	snp	A/C			intron-variant	LRSAM1	GRCh38.p7	9:127498992	AACCCAGGAGGCGGA[A/C]GTTACAGTGAGCCAA	90678
rs541433042	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127496605	TCACTGAATTCTCCC[A/G]ACAGCCCAGCAGGGT	90678
rs541434157	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127501657	GAATCGCTTGAACCC[A/G]GGAGGCAGAGATTGC	90678
rs541452067	snp	A/T	0.00199481	0.0315187	intron-variant	LRSAM1	GRCh38.p7	9:127458595	AAAATAAAACAAAAT[A/T]AAATAAAATTAAATT	90678
rs541468810	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127495571	AGTGGAGACAGAAGC[A/G]AGAGTAAGGGAGTGT	90678
rs541507008	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127497866	CCACCGCTGTGCATG[A/G]ACCACGTTGAGGAAC	90678
rs541604436	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127492667	GGGCCTCTTAGCTTT[A/G]TCCCCCAACGCAGCC	90678
rs541606397	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127484873	GAGTGCAGTGGCATG[A/G]TCTCAGCTCACGCAA	90678
rs541650725	snp	A/C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127485472	TGAGGAGGAGAATGG[A/C/T]GGGAACCTGGGAGGC	90678
rs541806458	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127455448	CCCTGGGCTCAGCAC[C/T]GCCACCTGCTGTGGC	90678
rs541876340	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127472239	TGCTGGGATTACAGG[C/T]GTGAGACACCACGCC	90678
rs541915102	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127450139	TTAAGTGCCAGCTAA[C/T]GGCCAAGGAAGAATA	90678
rs541954009	snp	C/G/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127496245	CAGATGGCCAGAACA[C/G/T]CTGCCCATCTGCCCC	90678
rs541963437	snp	C/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127480339	GTTGCACTGAGGTCA[C/G]CTGTTCACCTGTAGT	90678
rs541992899	snp	G/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127489185	CCATCTGTGAAGTGG[G/T]GCAGTAAAAGCACCC	90678
rs542027627	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127481543	GTGAGCCACTGCTCC[C/T]GGCCAAGGAGAGCAG	90678
rs542028105	snp	A/G	0.00159617	0.0282053	intron-variant	LRSAM1	GRCh38.p7	9:127489604	GGTCGCAGCAGTTGA[A/G]GTTTGAACCCCAGCT	90678
rs542077582	snp	A/G	2.7491e-05	0.00370739	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127467809	GCCGGCACTGCGGCC[A/G]TCTTGCAGTTCCTCT	90678
rs542273019	snp	A/G	0.00279162	0.0372561	intron-variant	LRSAM1	GRCh38.p7	9:127477916	CAGCCGGGTGTGGTG[A/G]TGGGTGCCTGTAATC	90678
rs542353303	snp	C/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127473684	GCCCAGGCTAGGGAA[C/G]AGGAGAGCAGTGGCT	90678
rs542423830	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127467344	GTGCCATCCACTGCG[C/T]GTGTCCCCAGGAGCT	90678
rs542497718	snp	A/C/T	0.000115314	0.00759241	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127461219	AGCTCCCACGTTCCA[A/C/T]TGGGAACCTGACCCA	90678
rs542525370	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127465469	CACAGTCCGTGCCCT[C/T]AAGCCACCACGCTTT	90678
rs542545755	snp	C/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127500852	GAAGAGAAGAAGAGA[C/G]TGTGTGGCAAGGAGA	90678
rs542587550	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127497896	CCTCCGGATCCATCC[C/T]GTGAGGAGGCACTGT	90678
rs542799580	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127471534	GCTCACGCCTGTAAT[C/T]CCAGCACTTTAGGAG	90678
rs542847791	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127458090	CATTTTCATTTTTAA[A/G]AAATTAGCAGTCAGT	90678
rs542861069	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127490384	GTGTCATAGGGACTT[A/G]GGGATGAGGGTCACA	90678
rs542885922	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127450885	TTCCGGGGTTGGACA[C/T]GCCACCCTCTGCCTC	90678
rs542947598	snp	G/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127459222	GCCCTTTGGGGTTTT[G/T]TTTTTTTTTTTTGAG	90678
rs543003414	snp	A/C/G			upstream-variant-2KB, intron-variant, utr-variant-5-prime	RPL12, LRSAM1	GRCh38.p7	9:127451754	CATTCCGAGACCCCA[A/C/G]TACCGCGGCGACCCC	90678
rs543044068	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127460288	CAGGTGTTAGCCACC[A/G]TGCCTGGCCCCCATT	90678
rs543079204	snp	C/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127460636	AGGCCTGGCTGTGCT[C/G]TCCTGAGCACGTGAC	90678
rs543080107	snp	C/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127467099	TTATTAGCTGGCAAC[C/G]GAGAGGCAGCTAATG	90678
rs543119820	snp	A/G	0.00159617	0.0282053	intron-variant	LRSAM1	GRCh38.p7	9:127454667	ATGGAGTAGGCCTCC[A/G]CACTGCCCCCAACAA	90678
rs543139061	snp	C/T	5.42353e-05	0.00520718	intron-variant	LRSAM1	GRCh38.p7	9:127502734	TGGGACTCCTGGAAC[C/T]CGGTAGGGCCAGCCA	90678
rs543139675	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	LRSAM1	GRCh38.p7	9:127454037	ACAGCCCCTGCCTCC[A/G]TGGAACTCAATAGAA	90678
rs543168598	snp	C/T	0.00279162	0.0372561	intron-variant	LRSAM1	GRCh38.p7	9:127494981	TTTGAGACGGAGTTT[C/T]GCTCTTGTTGCCCAG	90678
rs543263976	snp	G/T	0.00159617	0.0282053	intron-variant	LRSAM1	GRCh38.p7	9:127494950	CCATCATTTTGGTTT[G/T]GTTTTGTTTTGTTTT	90678
rs543396477	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127466382	GAAACCACTTTTAGT[C/T]TGATAGATATCCCTC	90678
rs543438561	snp	A/G/T	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127473522	CAGGTTTCACTGCTT[A/G/T]TCTCAGGCTTTTTCA	90678
rs543612655	snp	C/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127487478	CCCAGCTCCCAACTC[C/G]ATCCCCTTCCCTCCA	90678
rs543810943	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127492736	AGGCCCTTCTCCATC[C/T]TGCCACTGCGGGACT	90678
rs543877896	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RPL12, LRSAM1	GRCh38.p7	9:127453288	GGTTTGACCATGTTA[C/T]CCAGGCTGGTCTCGA	90678
rs543983279	snp	A/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127485610	TTAAGATAACTATCA[A/G]GTAGGTAACCAGGTG	90678
rs544025756	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127482268	CTGCCTCAGCATCCC[A/G]AGTAGCTGGGATTAT	90678
rs544050557	snp	A/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127479190	GTTGAGCCCAGCACC[A/G]GGCTCTAGACCACTA	90678
rs544184871	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127480534	GCCTCTTTTTTCTAA[C/T]CCTGAATCACTCGTT	90678
rs544260312	snp	G/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127474990	TGACTCTTAATCTCT[G/T]GTTCCTAGATGCCAC	90678
rs544268046	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127450189	AAGACCAATGGGGAA[G/T]AGCATTTGGGGCAGG	90678
rs544382632	snp	G/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127482894	GGTGTTCATCTGCTG[G/T]GATTCCCTGTTGGAA	90678
rs544469133	snp	C/T	0.00318978	0.0398085	intron-variant	LRSAM1	GRCh38.p7	9:127470222	TGAAGAAATTCTTTA[C/T]AAAGAAAAGAAGTTT	90678
rs544469793	snp	A/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127468804	CATGGTGAAACCCTG[A/T]CTCTACAAAAAAAAA	90678
rs544494139	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127501684	TTGCAGTGAGCCAAG[A/G]TCCCACCACTGCACT	90678
rs544506550	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127461656	CTGGGCAGGCTGAGG[A/G]CAGTGGTGCCATCCC	90678
rs544532642	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127495658	ACTGAGCCCACAGTA[A/G]AGCAAAGCCTGTGCC	90678
rs544538830	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127502466	GAGGCGGGCAGATCA[C/T]TTGGGGTCAGGAGTT	90678
rs544729482	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127464937	GTGAGCCACCACACC[C/T]AACCTGGACACTTCA	90678
rs544883338	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127456275	GCTCTGCTCTGTCAC[C/T]CAGGCTGGAGTGCAG	90678
rs544896032	snp	C/G	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127498652	TGCTTGTGCCCATTG[C/G]CAGGGGAAGGGGCCA	90678
rs544921241	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127449511	AAGGTGAAATCACTC[C/T]CGGCTCACCACTGGT	90678
rs544927171	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127456966	CATGAGCTTTTATTT[A/G]ACATCATGGCAGCCC	90678
rs544928820	snp	C/T	3.93298e-05	0.00443434	intron-variant	LRSAM1	GRCh38.p7	9:127492772	GCTGCCGCCAGCTCA[C/T]GGTGGTGCGGGGTGT	90678
rs544932725	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127499307	TGAGCTTGGGAGGTC[A/G]AGGCTGCAGTGAGCC	90678
rs544937969	snp	A/G	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127460093	CAATCTCCACCTCCC[A/G]GGTTCAAGCGATTCC	90678
rs544985576	snp	C/T	0.00358779	0.0422022	intron-variant	LRSAM1	GRCh38.p7	9:127465941	GCATCTGCATGTGTG[C/T]GCTGATAAACATTTG	90678
rs545053269	snp	A/T			intron-variant	LRSAM1	GRCh38.p7	9:127476322	CTATTTCCATTCTTA[A/T]GTTTAAAAAGAAAAC	90678
rs545100438	snp	A/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127457743	ACTCCCTGCTGACTG[A/T]GAGCTCCTCCCCGGA	90678
rs545126671	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127481644	ATTCACCTCCTTAGA[C/T]GATATTTAATTACAA	90678
rs545215518	snp	G/T	0.00318978	0.0398085	intron-variant	LRSAM1	GRCh38.p7	9:127459274	CAGGCTGGGGTGCAG[G/T]GGCGCCATCAGAGTT	90678
rs545234557	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, splice-acceptor-variant, utr-variant-5-prime	RPL12, LRSAM1	GRCh38.p7	9:127451927	TGAGTTTCTGTTCCC[A/T]GCACCTGCCTTTGAA	90678
rs545237400	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127491120	GCCTCCCCAGAAAGG[C/T]TTCTTAGACCCACTT	90678
rs545272402	snp	A/C	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127483780	GCGATTCTCCTGCCT[A/C]AGCCTCCGAGTAGCT	90678
rs545289937	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	RPL12, LRSAM1	GRCh38.p7	9:127453361	TGCTGGGATTACAGG[C/T]ATGAGCCACCACACC	90678
rs545447159	snp	A/G	0.00279162	0.0372561	intron-variant	LRSAM1	GRCh38.p7	9:127458158	GGCCAAGGCGGGTGG[A/G]TCACTTGAGGTCAGG	90678
rs545516690	snp	A/G	0.000131798	0.00811675	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127461184	TTAGGTCTTAAACGT[A/G]GAAAGGAATCAACTG	90678
rs545553301	snp	A/G	0.00159617	0.0282053	intron-variant	LRSAM1	GRCh38.p7	9:127455382	GTCTCCTGCCAGCTG[A/G]CCGAGGGAAGGGCTG	90678
rs545567782	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127500798	TCCCTGCAGAGAGAG[A/G]CTTCACTCCCATTCT	90678
rs545583135	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127497816	AGTCTGGGGTCTGCC[A/G]TGTGCTGAGCATGAT	90678
rs545585528	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127491932	CTCTCCAGCTGCAGA[C/T]GGAGGGCTGGATGGG	90678
rs545615822	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127454686	TGCCCCCAACAAGCC[A/G]TGCTCCTTCCCATCT	90678
rs545617694	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127483230	ACCATGTGACCTTAG[A/G]GACATTACTGCTTAC	90678
rs545692903	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127497622	GTCCACCCTACAGAC[A/G]CTGGGATCCACACAC	90678
rs545756011	snp	C/T	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127493369	GCCTAGCCTCTCCTG[C/T]GGTTTTGATGCATAT	90678
rs545766750	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127500061	GCTCACGTTGCATGA[C/T]AGAAAAAGAGACTTA	90678
rs545783565	snp	A/C/G	0.00239393	0.0345281	intron-variant	LRSAM1	GRCh38.p7	9:127460769	TGCCTGGGTGCCCTG[A/C/G]CCCGGCAGGGCGAGG	90678
rs545814024	snp	A/G	0.000419473	0.0144762	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127467781	GGTCTACCCGCCGCG[A/G]GAGGTGTGTGGTGCC	90678
rs545818806	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127481342	AGTGCAACCCCCGCC[A/G]CCCAGGTCCAAGCAA	90678
rs545820339	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127454747	CTTAGACCCAACAGA[C/T]GAGGCCCCCTGCCAA	90678
rs545930137	snp	C/T	0.00159617	0.0282053	intron-variant	LRSAM1	GRCh38.p7	9:127466777	CAGCACTTTGGGAGG[C/T]GGGCGAATTGCTTGG	90678
rs545946062	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127495045	CAACCTCTGCCTCCC[A/G]GGCTCAAGAGATTCT	90678
rs545947282	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127488482	GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCAG	90678
rs545981315	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127480747	GGCTGGAGTGCAGTG[A/G]TGTGCTCTCGGCTCA	90678
rs545983239	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127495481	CTCCCAGAGGCGCCT[A/G]TGGTGCCTCCACCAT	90678
rs546021734	snp	A/C/T			intron-variant	LRSAM1	GRCh38.p7	9:127469943	GCACTCCAGCCTGGG[A/C/T]TACAGAGCAAGACTC	90678
rs546021897	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127489099	TGCCTTGTGGTTAAG[C/T]GGGGCTCGGGAGCTG	90678
rs546189907	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127489594	CAGGGCGGCAGGTCG[C/T]AGCAGTTGAGGTTTG	90678
rs546261496	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127470914	TCTCAATTGATTGCT[C/T]ACAGTCAGTTACAGA	90678
rs546350572	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127461482	CCAGGGCCGTATGGC[C/T]GTATGGGGAGGAGGG	90678
rs546480778	snp	G/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127467130	CTCAAAATTCTCTTG[G/T]CCCTGAGGAAGGGGC	90678
rs546497500	snp	C/T	1.65285e-05	0.00287471	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127457366	GCTTCCCAAATCCTG[C/T]AGCCTCCTGAGTCTG	90678
rs546536234	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127450592	TTCCTAAGGTACCTA[A/G]TACTTGTTCAGTGGC	90678
rs546541056	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127482451	CCCGGCCATGTGACT[A/G]TTTGTGAAGGAAATA	90678
rs546579755	snp	A/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127475875	CCTCCCGAGTAGCTG[A/G]GATTACAGGGATGCG	90678
rs546625980	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127469382	GGCTGAGGCAGGAGA[A/G]TCACTTGAACCCGGG	90678
rs546701859	snp	A/G	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127461335	TCCACAGGCTGCCCC[A/G]CCCGGGAGCCATTGA	90678
rs546739304	snp	C/T	1.64754e-05	0.00287009	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127455582	TTATCTTAGATTCCA[C/T]TTGGAGCTTTTGCAA	90678
rs546745267	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127495731	GTTGAAACAGCCCCC[C/T]CTTGGTGGATGTTCA	90678
rs546745297	snp	A/C	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127488902	TTCAGCTCTTTCCTG[A/C]AGCCCCGTGGGAGTC	90678
rs546755217	snp	A/G	3.30901e-05	0.00406743	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127501084	TCTGTGAGGCCATCC[A/G]CTCCCCCTGCAGAGC	90678
rs546764161	snp	A/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127469868	TACTAGGGAGGCTGA[A/G]GCAGGAGAATGGCGT	90678
rs546830328	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127457772	GATGGGCTGGGAGGC[A/G]TTCACAACATGTGGG	90678
rs546870921	snp	A/G	0.000798403	0.0199641	downstream-variant-500B	LRSAM1	GRCh38.p7	9:127503630	CGCCGCACCTCAGTC[A/G]AGAGGAGAGGTCAGG	90678
rs546907838	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127497157	TCCAGCAGGAGGTGT[C/T]GACGGTCCTGTGAGC	90678
rs546955160	snp	G/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127460905	CTGTTGCCCAGGCCG[G/T]AGTGCAATGGTGCAA	90678
rs546967446	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127457893	AGCAGCACAGGCCCA[A/G]TCTGTTATACTATAT	90678
rs546970371	snp	C/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127465107	CCAAACAGCCCACCA[C/G]GTCGGTAACACTGCC	90678
rs547011071	snp	C/T	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127458949	CAGCGCTCTGGAGCC[C/T]GGAGTCTGAGGGACT	90678
rs547084915	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127501888	ATTCCAGGGTCTCCC[A/G]TTGACCTGACTCATG	90678
rs547159150	snp	C/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127485128	TAATTTGTTTAATTC[C/G]TAAATGCATAAAAAC	90678
rs547314101	in-del	-/TTC	0.00953873	0.0683987	intron-variant	LRSAM1	GRCh38.p7	9:127490248	TTTCTTTCTCTATTT[-/TTC]TTTCTTTCTTTCTTT	90678
rs547468770	snp	A/G	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127498118	GCATTTTTAGCCAGA[A/G]CCAAGGAAGAAGCGG	90678
rs547482275	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127483229	CACCATGTGACCTTA[A/G]GGACATTACTGCTTA	90678
rs547569733	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127496828	TCACAAGGCCATGCC[A/G]CTCAGGCTCTGGAGG	90678
rs547571500	in-del	-/C	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127469014	ATCAAAATGTCTCTT[-/C]CTCAAAAGATACCAT	90678
rs547620786	in-del	-/G	0.00716266	0.059414	intron-variant	LRSAM1	GRCh38.p7	9:127462704	GGAGGGAGAGCATCA[-/G]GAAGAAAAGCTAATG	90678
rs547632953	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127494180	ATCCGGCTCCTGGGC[A/G]CTGGAAGAGAGGGGC	90678
rs547687156	snp	G/T			intron-variant	LRSAM1	GRCh38.p7	9:127482232	ACTGCAACCTCCACC[G/T]CCCAGGTTCAGGCGA	90678
rs547714044	snp	A/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127478840	GTGGGCCAGAGTTTG[A/T]ATAACATCAGGCCAC	90678
rs547723425	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127478642	TCCTGCTCTGCTCTT[C/T]AGACCACCATCCCTG	90678
rs547729875	snp	A/G	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127464451	CGGCAGCCGCTGGCC[A/G]TATGTATCTATGGAG	90678
rs547765163	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451119	CCTACACGTGAAGAA[A/G]CTAAGGCCCAGAAAG	90678
rs547820933	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127471741	GCAGTGAGCTGAGAT[C/T]TCGCCACTGCACTCC	90678
rs547903426	snp	C/T	1.84137e-05	0.00303422	intron-variant	LRSAM1	GRCh38.p7	9:127491347	GGTGAGACCCCCACC[C/T]GGTGCTCCCTCCCAG	90678
rs547939145	snp	C/T	0.00159617	0.0282053	intron-variant	LRSAM1	GRCh38.p7	9:127477515	AGCACTTTGGGAGGC[C/T]GAGTCGGGTGGATGC	90678
rs547941645	snp	C/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127484078	AGTAAACACTAACTC[C/G]CCGTGCCCCCCTCCC	90678
rs548063936	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127474661	TTCATTGCTATCTCT[C/T]AGCAAATACTTCTGG	90678
rs548086636	snp	G/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127478630	AGATATCCCATTTCC[G/T]GCTCTGCTCTTCAGA	90678
rs548179082	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127487787	TCGCCCAGAGCCTGA[A/G]GGTGGGAGCTCAGGA	90678
rs548270854	snp	C/G	0.000297349	0.0121896	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127479448	GCAGCGGGAGCACAC[C/G]CAGCTCCTTCAGCAG	90678
rs548350678	snp	G/T	0.0023933	0.0345097	intron-variant	LRSAM1	GRCh38.p7	9:127480799	TTCAAGCAATTCTCT[G/T]GCCTCAGCCTCCCAA	90678
rs548401371	in-del	-/ATA			intron-variant	LRSAM1	GRCh38.p7	9:127466502	TATATATATATATAT[-/ATA]TTTTTTTTTTTTTTT	90678
rs548447994	in-del	-/A			intron-variant	LRSAM1	GRCh38.p7	9:127475503	CCATCTCAAACAAAC[-/A]AACAAACAAACATTT	90678
rs548479612	snp	A/G	7.00403e-05	0.00591737	intron-variant	LRSAM1	GRCh38.p7	9:127491330	CCTGCCCTCCTTCAC[A/G]TGGTGAGACCCCCAC	90678
rs548485151	snp	A/C	0.140242	0.224618	intron-variant	LRSAM1	GRCh38.p7	9:127501164	TCCGGGGCCCTCCCC[A/C]CCCGCCTGCCCTGCC	90678
rs548554280	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127476521	ACCACTGCACCCCAT[C/T]CTGAGTAACAGAACT	90678
rs548619801	snp	G/T	0.00159617	0.0282053	intron-variant	LRSAM1	GRCh38.p7	9:127466033	AAACATTTCTGCCAG[G/T]CACAGTGGCTCAAGC	90678
rs548689653	snp	G/T	0.000399281	0.0141238	downstream-variant-500B	LRSAM1	GRCh38.p7	9:127503720	GCCCAGAGGCAGCCA[G/T]GGCCGGTGATGGCTG	90678
rs548793451	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	LRSAM1	GRCh38.p7	9:127454345	CCCAGCCGCTGCCTC[C/T]GTGGAACTCACTAGG	90678
rs548857122	snp	A/G	0.00159617	0.0282053	intron-variant	LRSAM1	GRCh38.p7	9:127493732	TCCCCTGATGGGTTT[A/G]ACACTGGCACATTTT	90678
rs548898578	snp	A/T			missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127478958	TCAGACTATGAGAAG[A/T]GGAAGGTAAGAAAAT	90678
rs548935308	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451166	GGCGGCGCAACACCG[A/G]GAAGGTCTCTGGGAG	90678
rs548956595	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127456039	ATAATAGAAACTCAC[A/G]CCTTTTATTCTGGTC	90678
rs548958613	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127461869	TCTGTTTATCAACTG[C/T]AACATATGAGTAATG	90678
rs548978792	in-del	-/GGGGC	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127490138	TCACCGCCTGTGGAG[-/GGGGC]TGGGGCTGGGGCTGG	90678
rs548979471	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127470406	CCACCATAAGAATAG[C/T]ATGGGGGAACTGCTC	90678
rs548993529	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127456551	TGGAAGTGTTGGGCC[A/G]CAGTCAATGCCTAAG	90678
rs549004409	snp	G/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127490678	GGCAATAATACCTCC[G/T]AGCAGCCAGAGAATT	90678
rs549033948	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127457191	CTGACCCGCATCCCC[A/G]TGGTGGTGTCTGGGA	90678
rs549046262	snp	A/G			intron-variant, utr-variant-5-prime	LRSAM1	GRCh38.p7	9:127453559	TGATCCTGCTCTGAC[A/G]GCGTTTGGGGGGCTA	90678
rs549109596	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127471744	GTGAGCTGAGATCTC[A/G]CCACTGCACTCCAGC	90678
rs549138571	snp	A/G	0.0023933	0.0345097	intron-variant	LRSAM1	GRCh38.p7	9:127481882	CCAACATGGCAAAAC[A/G]CTGTCTCTACTAAAA	90678
rs549175761	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127449780	ACCTGCCCACCACTT[C/T]TCACTTGGCAACAAA	90678
rs549177065	snp	C/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127482553	AGTGTAGGAAAGTGC[C/G]CATTTCTCCACCACC	90678
rs549230042	snp	A/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127458307	GAATGGCGTGAACCC[A/G]GGAAGCGGAGCTTGC	90678
rs549258102	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127497600	CCTGTCCCATAGCCT[C/T]CCCTCAGTCCACCCT	90678
rs549266769	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451403	CGAGCCGAAAGCCGA[A/G]AGGCCGGAAATCGCG	90678
rs549294693	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127491479	CCCAGAAGGCCCAGC[A/G]CAGGCCAAGGTTAGA	90678
rs549306433	snp	A/G			intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127449944	CCTAAGTGCCCATGT[A/G]CTTAAGGAGGGGGAT	90678
rs549312299	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127483036	GTGAGTTTTGGGATG[A/G]GGAGCTTGTGAGCAC	90678
rs549334231	in-del	-/TTATTA	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127475048	AATGCATTTGGGATT[-/TTATTA]TTATTATTATTATTA	90678
rs549395685	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	LRSAM1	GRCh38.p7	9:127453562	TCCTGCTCTGACAGC[A/G]TTTGGGGGGCTAGAA	90678
rs549432449	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	LRSAM1	GRCh38.p7	9:127454126	AACTCACTAGAAAGA[C/T]GCAGCCCCTGCCCCC	90678
rs549459286	snp	A/G	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127475902	TGCGCCACCATGCCC[A/G]GCTAATTTTGTATTT	90678
rs549468112	snp	A/G	0.00279162	0.0372561	utr-variant-3-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127502956	GCCACTGTGAGCCCC[A/G]GGCTCCTGCTCAGCC	90678
rs549577500	snp	A/C/T	0.000851501	0.0206164	intron-variant	LRSAM1	GRCh38.p7	9:127479542	GTCCAGCCTGGCTGC[A/C/T]TCCCCCAGCCAGTGG	90678
rs549645261	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127493495	CATTCTTTTCAAGTC[A/G]TTAAACTATTCCTTG	90678
rs549682283	snp	A/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127486678	CCCACTTCTGCTTAC[A/T]AACCGTGAGGTCTCA	90678
rs549714184	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127473135	TGAATATTTTTCATA[C/T]GTCTCCTGCCCATTT	90678
rs549846462	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127492954	GCTTTTCTTTAACAG[A/G]CTTGCCATTTTTAGA	90678
rs549882753	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127491988	GCCAGGAGTTTGAGC[A/G]GAGCCTTCGGTCTGT	90678
rs550151056	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127499514	CCAGCCTGGGTGACA[A/G]AGCAAGACCCTGTCT	90678
rs550159592	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127465861	AACACAACTCACACC[A/G]TGGATGGGGCAGTTC	90678
rs550209823	snp	G/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127477623	GGCATGGTGGTGCGT[G/T]CCTGCAGTCTCAGCA	90678
rs550326929	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127471867	AGGGTTTCGCCATGT[C/T]GACCAGGGTGGTCTC	90678
rs550346445	snp	A/C	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127478171	ACATTATTGATGTTT[A/C]ATACCTGCTCCTTGT	90678
rs550363764	snp	C/T	0.00159617	0.0282053	intron-variant	LRSAM1	GRCh38.p7	9:127465202	CAGCATGCAATGAGC[C/T]GGGATCTGAAGCCAT	90678
rs550477853	snp	C/T	0.00159617	0.0282053	intron-variant	LRSAM1	GRCh38.p7	9:127469300	CATGGTAAAACTCCA[C/T]CTCTACTAAAAATAC	90678
rs550516436	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127461987	AATCTCCCCGTGTTC[C/T]TATAAGGCTGGGTGG	90678
rs550546958	snp	C/G	3.29489e-05	0.00405874	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127473823	GCTGGAATACTACCC[C/G]CCTTCTCAGTACTTG	90678
rs550606942	snp	A/C	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127481601	TCCAGAGGATTATGC[A/C]AGGACATTTCCCTAA	90678
rs550713792	snp	C/T	0.00318978	0.0398085	intron-variant	LRSAM1	GRCh38.p7	9:127467374	TGCTGGTGCAGCTCA[C/T]CTCAATATCTTATCA	90678
rs550750752	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127460878	TTTTTTTTTTTGAGA[C/T]GGAGTCTCACTCTGT	90678
rs550792745	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127487805	TGGGAGCTCAGGAGG[A/G]AGGTTCAGGAGCCAG	90678
rs550802655	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127462561	TGACTTTTGCTGCCA[C/T]AATAGAGGCAGAAAA	90678
rs550807542	snp	A/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127469836	AAGGCGTGGTGGCGG[A/G]CGCCTGTAGTCCCAG	90678
rs550874368	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127502167	GCGGAATAGGCCTCC[A/G]TCGCCTGTCCAGAGC	90678
rs550949332	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127470971	CTCTTCTCACCGCTG[C/T]ACTTGACTAATCTTA	90678
rs550974434	snp	A/C			upstream-variant-2KB, intron-variant	RPL12, LRSAM1	GRCh38.p7	9:127453313	TCTCGAACTCCTGGG[A/C]TCAAGTGACCCACCT	90678
rs550981758	snp	A/C	0.00398564	0.0444627	intron-variant	LRSAM1	GRCh38.p7	9:127495187	TGAACTCCCGACCTC[A/C]GGTGATCTGCCCACC	90678
rs551018294	snp	A/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127488723	CTTTGCCTCCTGAGT[A/G]GCGGAGACCACAGGG	90678
rs551062258	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127454829	CATCCCTCTGGGCCT[C/T]AAGCTCTGGGAAAGC	90678
rs551105962	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127494636	ACGAAGAGTTATCGA[A/G]TGGCAGAATAAAAGA	90678
rs551116887	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127491635	CTCTCTGTAGGCCGT[A/G]CTTTAGGCCCCCAGG	90678
rs551117117	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127497981	CCCCATCAGGTCCCA[C/T]TGCTGGCAGATGGTG	90678
rs551183702	snp	A/G	0.000131774	0.00811601	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127455028	GCAGATGACATTCTC[A/G]ACATCTCTAAATGTG	90678
rs551222373	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127455487	CTTGTTCACCTCCTG[C/T]CTGTCTCTTCCTCAC	90678
rs551225858	snp	G/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127458246	AATTAGCCGGGCGCG[G/T]TGGCGGGCGCCTGTA	90678
rs551352437	snp	C/T	1.67103e-05	0.00289048	intron-variant	LRSAM1	GRCh38.p7	9:127457288	TGCTCTTCCTCAGCC[C/T]AGCATGGCCGCACAT	90678
rs551417285	snp	C/T	0.0023933	0.0345097	intron-variant	LRSAM1	GRCh38.p7	9:127458367	GCAGTCCGGCGTGGG[C/T]GACAGAGCGAGACTT	90678
rs551504680	snp	A/C			intron-variant	LRSAM1	GRCh38.p7	9:127497584	GGGGCCCTCCCAGCT[A/C]CCTGTCCCATAGCCT	90678
rs551523391	snp	C/T			utr-variant-3-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127503222	TTGACTGAAGGCCAC[C/T]GCCCCTGCAGGAGCT	90678
rs551559665	snp	A/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127476651	TGAAGTGGCATGAGC[A/G]AATTTTCGAGGGTGA	90678
rs551599331	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451429	TCGCGCGGACAAGCC[A/G]GATATAGGCAGGAAA	90678
rs551680347	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127485005	TACAGACACAGTTTC[A/G]CCATGTTGGCCAGGC	90678
rs551709638	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127475035	CACTGCTGCTGGGAA[C/T]GCATTTGGGATTTTA	90678
rs551751115	snp	C/T	0.00159617	0.0282053	intron-variant	LRSAM1	GRCh38.p7	9:127496681	AACTTGGCCCAAGGT[C/T]ACACAGCAGAGTGAG	90678
rs551775913	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127475833	GCAACCTCCATCTCC[C/T]GGGTTCAAGTGATTC	90678
rs551836569	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127459566	TGGTGTAGGACTTTT[C/T]GTATGTGTATTTTTT	90678
rs551863360	snp	A/C/T			intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127450477	CCTAACTTCAAAACT[A/C/T]CCCCTTGGGCCCACC	90678
rs551879236	snp	G/T	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127490430	GATAGAGAAGTACTG[G/T]CTATGGGGTCTGACC	90678
rs551883007	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	LRSAM1	GRCh38.p7	9:127454196	AACTCACTAGAAAGA[C/T]GCTGTCCCTGACCCC	90678
rs551894704	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127497106	CTGCCTCATCCTGAC[C/T]GTGGGCCCCGCCAGG	90678
rs551914141	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127483131	CTGAGTGTTAGCCCT[C/T]GAGAGGGGCAGTCAA	90678
rs551957380	snp	A/G	0.00054351	0.016476	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127473887	TCTCGGGACAGCCCT[A/G]ATGGGCCCACGGACA	90678
rs552015477	snp	C/T			upstream-variant-2KB, intron-variant	RPL12, LRSAM1	GRCh38.p7	9:127452656	GTCGCTGGATCCTCA[C/T]AGAAGCCAGTGTTGG	90678
rs552093967	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127474542	CCTTGGTAGCACTTA[C/T]CACAGCGCTAAATTG	90678
rs552158273	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127493543	TGTCCGTGGCCCCTA[C/T]TGTTGAGTATGTGGA	90678
rs552243567	snp	A/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127486793	TGAGTGTTGATGAGC[A/G]TAATCTCTAGTGCAT	90678
rs552252801	snp	A/C	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127485670	TGGAAATCCCTGCTG[A/C]CTCCCTGCCCAGGTG	90678
rs552266833	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127468016	AATAGATACAGACTG[C/T]GGTTATGGGAGTGCA	90678
rs552291864	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127478795	ATCCCCTCATCCCCC[A/G]ACCCCACCATTCTGA	90678
rs552458963	in-del	-/AATA	0.00676609	0.0577691	intron-variant	LRSAM1	GRCh38.p7	9:127501364	TTTTTGTTCCTACTT[-/AATA]AATACATTAGGAAAA	90678
rs552509935	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127478419	ATTCGCCCCATTGGC[A/G]GTTGTGTAATAGTCC	90678
rs552549827	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127488859	GCCTCCCAGAGTGCT[A/G]GGATTACAGACATGA	90678
rs552557812	snp	G/T	0.00199481	0.0315187	intron-variant	LRSAM1	GRCh38.p7	9:127460320	CATCTATTTTTAATG[G/T]TTAGTGTGTCATCCT	90678
rs552689988	snp	A/G	0.000139477	0.0083498	intron-variant	LRSAM1	GRCh38.p7	9:127496140	GGGGCACGCAAGGCC[A/G]CTGTCCTGACCAGCC	90678
rs552743555	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127457190	ACTGACCCGCATCCC[C/T]GTGGTGGTGTCTGGG	90678
rs552759545	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127459755	GTAGAGACTTGTTTT[C/T]ACCATGTTGGCCAGG	90678
rs552798222	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	LRSAM1	GRCh38.p7	9:127453641	AAGCACCTGAGGAAA[C/T]GTCTCTAAGTTTCCC	90678
rs552839524	snp	A/G	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127456151	AAGTGAAGTATCTAA[A/G]TGAGAATATGCAAAA	90678
rs552908625	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127494056	ACTTTGCAGATGGTG[C/T]CTTGGCGCTGTGCCT	90678
rs552917918	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127499653	TCTTTAGTTGTGGCC[A/G]GGTGCGGTGCCTCAC	90678
rs553011658	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127461576	GAGAGCTCCTAAGGA[A/G]CCGCAGTAAGGTTCT	90678
rs553023644	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127482051	CCATTAAATGTCTTA[C/T]TGAATAATATTTCTC	90678
rs553074777	snp	C/T	1.67399e-05	0.00289304	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127454532	AAAAGGGAAGGATGC[C/T]GCTCTTCTTCCGGAA	90678
rs553084262	snp	G/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127487927	TGAGGGGTGGGAGAG[G/T]CTGAGGGGGGGCCCG	90678
rs553124099	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127495482	TCCCAGAGGCGCCTG[C/T]GGTGCCTCCACCATG	90678
rs553153174	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127449958	TGCTTAAGGAGGGGG[A/C]TTTTCAGCCCTGCTG	90678
rs553162828	snp	G/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127496210	TGTCCTTACCTAATG[G/T]CCCAGGGCCACCTTG	90678
rs553246426	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127480323	GGGTTCTGCGTAACC[C/T]GTTGCACTGAGGTCA	90678
rs553300111	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127489584	AGTGGCCCTCCAGGG[C/T]GGCAGGTCGCAGCAG	90678
rs553351622	snp	A/G	1.64743e-05	0.00287	intron-variant	LRSAM1	GRCh38.p7	9:127455097	AATTGGATCTGTCCC[A/G]TTTTCTTGGATCTTG	90678
rs553447031	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127497696	CCTGCAGTATACCCA[A/G]TGCTGGGCCTGAGGC	90678
rs553510399	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	RPL12, LRSAM1	GRCh38.p7	9:127451524	TGTTGTGGGCAGGCG[C/T]CTGAGGCTGACGGCT	90678
rs553637839	snp	A/G	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127490400	GGGATGAGGGTCACA[A/G]GGTCATGGGCACAGG	90678
rs553664482	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127483087	GCAGGGTGGATGGCC[C/G]TCCCTCTGTTGGCCA	90678
rs553800504	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127462994	TGAGGTTAGGAGTTC[A/G]AGACCAGCCTGGCCA	90678
rs553850810	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127475698	AATTGGTATCACAAC[C/T]TTGGAGGATAATTTG	90678
rs553891721	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127470127	ACATTCAAATATCCT[A/G]TGGCCCATGAGTTCC	90678
rs553926707	snp	C/T	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127463089	GTAATCCCAGCTACT[C/T]GGGGGAGGCTGAGAC	90678
rs553936753	snp	A/C	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127471462	GGTGACAGAGAGAGA[A/C]CTTATGTTATAAAAA	90678
rs553953439	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127463959	AGGGCCACACAGTCA[C/T]TGACAGCAGAGATCG	90678
rs553984178	snp	A/G	0.00358779	0.0422022	intron-variant	LRSAM1	GRCh38.p7	9:127466365	AAAATCTCCTTTTAG[A/G]GGAAACCACTTTTAG	90678
rs554034484	in-del	-/CTAT	0.00676609	0.0577691	intron-variant	LRSAM1	GRCh38.p7	9:127495799	AGTGAACCCCTGGGC[-/CTAT]CTATCTATCTATCTC	90678
rs554058562	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127471577	GGATCACCTGAGGTC[A/G]GGAGTTCGAGACCAG	90678
rs554114301	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127503241	CCTGCAGGAGCTTGG[C/G]TCCTCATCTGGGGGC	90678
rs554143588	snp	A/C	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127476189	CCCCAAATGTTTGTC[A/C]GTGAGAAGGCACTGC	90678
rs554359699	snp	A/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127461011	CAGGTGTGTGCCACC[A/T]TGCCCAGCTAATTTT	90678
rs554369287	snp	A/G	0.0023933	0.0345097	intron-variant	LRSAM1	GRCh38.p7	9:127461605	CTGAGCAGTGCTTCC[A/G]CCTCCAGCGACGCAC	90678
rs554398886	snp	A/G	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127455172	AGAAGCTCTAGTCAC[A/G]AGATGTTTCCTTAGA	90678
rs554466701	snp	A/G	3.31851e-05	0.00407326	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127497283	GCTGGCCTGCAGCAC[A/G]AGATCCTCCGGAGAG	90678
rs554575696	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127479716	CTGGGAGGAGCTGGC[C/T]GGAGGTCACACAAAA	90678
rs554583477	in-del	-/A	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127491184	GTGGTTAATGTGAGT[-/A]AAAAAAAACCCTGTC	90678
rs554785781	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127499186	GAGACCAGCCTGGGC[A/G]ACATAGGGAGACCCC	90678
rs554827021	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127493186	CCCACCTCAGCTTCC[C/T]GAGTAGCTGGGACTA	90678
rs554855758	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	LRSAM1	GRCh38.p7	9:127453724	TGGGCCCCAACCCAG[A/G]TCATCTGGCTTGTCT	90678
rs554866051	snp	G/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127494945	CATAACCATCATTTT[G/T]GTTTTGTTTTGTTTT	90678
rs554983278	snp	A/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127465374	ATGGACTCAAACTTT[A/T]AATCAGATTTATTTT	90678
rs555018250	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127459148	AGCCTGGAATGTTCT[A/G]GCCGGGCTCCAGCCA	90678
rs555032177	in-del	-/GGCCACAGCACTGCCTGA	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127496424	GTCACAAACTGTCGT[-/GGCCACAGCACTGCCTGA]GCCCCTGTTCCTTTC	90678
rs555056669	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127459806	TCAGGTGATCCACCC[A/G]TCTTGGCCTCCCAAA	90678
rs555098979	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127467585	CCAGGCACTGGGAAC[A/G]CAGCTGTAAGTAACA	90678
rs555119305	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127450150	CTAACGGCCAAGGAA[A/G]AATAGTTAAGATACA	90678
rs555124453	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127492676	AGCTTTGTCCCCCAA[C/T]GCAGCCTGGAGGCAT	90678
rs555147792	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127496264	CCCATCTGCCCCAGC[C/T]GCCTGTGTGTGCCCT	90678
rs555184727	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127489638	TGGCTTGCTAGCCCA[A/G]CAAGAGGTCGAGGCC	90678
rs555301295	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127488033	GTGTAGGAGGCTCCA[C/T]TGGAAGGACTTAAGT	90678
rs555334757	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127486949	GCACTTTGGGAGGCC[A/G]AGGTGGGTGGATCAC	90678
rs555377969	snp	A/G	8.24083e-05	0.00641852	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127462281	GAGCTTCCAGACACC[A/G]TGGGGGAGCTTCGAA	90678
rs555414764	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127456903	AAAAATAGCAGTAGA[C/T]GACCTGGACTGAGCC	90678
rs555440182	snp	A/G	0.00199481	0.0315187	intron-variant	LRSAM1	GRCh38.p7	9:127480388	CCCTGTGCAAGGTAC[A/G]AGCTAGTAAGAGCAG	90678
rs555440275	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127488922	CCGTGGGAGTCTTGC[C/T]GCTGCCTCCCTTCTT	90678
rs555531911	snp	A/G	7.8855e-05	0.00627864	intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127450708	AAATGTGAAAAAAAT[A/G]CCCCTTGGAGGGGAT	90678
rs555607901	snp	C/G			intron-variant, utr-variant-5-prime	LRSAM1	GRCh38.p7	9:127453548	ATTGCTCCTGCTGAT[C/G]CTGCTCTGACAGCGT	90678
rs555654344	snp	G/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127474959	GCTGCCGGGCATTTG[G/T]CTTCATATCTTCCAC	90678
rs555690877	snp	A/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127484632	CCCGTAAGTGCTTAT[A/G]TTACAGGTGAGCCGC	90678
rs555736418	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127483334	TGCCTGTAATCCCAG[C/T]GCTTTAGGAAGCCGA	90678
rs555736511	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127476278	ATGGATTAGTGAAAA[A/G]GGCAGATTGCAGAAC	90678
rs555779807	snp	A/C			intron-variant	LRSAM1	GRCh38.p7	9:127469821	ACAAAAAAAATTAGC[A/C]AGGCGTGGTGGCGGG	90678
rs555975925	snp	C/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127485306	GGCTCACCTGTAATC[C/G]CAGCACTTTGGGAGG	90678
rs556183402	in-del	-/TT			intron-variant	LRSAM1	GRCh38.p7	9:127498728	TTCCTAGCAATTCTC[-/TT]TTATTACTCCCAGAA	90678
rs556201183	snp	A/C	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127474249	CCACTCACTTGTCTT[A/C]TCCTTCAGTTCTTTT	90678
rs556236953	in-del	-/ATATATA			intron-variant	LRSAM1	GRCh38.p7	9:127466494	TATATATATATATAT[-/ATATATA]TATATTTTTTTTTTT	90678
rs556256875	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127466805	TGGGCCCAAGACTTT[C/G]AGACTAGCCTGGGTA	90678
rs556277432	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127462920	AGATTTCTGGGCTGG[A/G]CACCGTGGCTCACTC	90678
rs556298567	snp	A/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127472107	GCTGGGATTACAGGC[A/G]CCCACCACCACGCCT	90678
rs556317767	snp	A/G	0.00199481	0.0315187	intron-variant	LRSAM1	GRCh38.p7	9:127458147	GCACTTTGGGAGGCC[A/G]AGGCGGGTGGGTCAC	90678
rs556340793	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127481528	ACTGGGATTGCAGGC[A/G]TGAGCCACTGCTCCC	90678
rs556391869	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant, utr-variant-5-prime	RPL12, LRSAM1	GRCh38.p7	9:127451819	TATCAAAACAGTCTA[C/T]GTGGAAATCCAGTCC	90678
rs556491097	snp	A/G			utr-variant-3-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127503308	GAGCAGGAGGGCCTG[A/G]CTGGGTGAGGGGAGG	90678
rs556521862	snp	A/C			intron-variant, utr-variant-5-prime	LRSAM1	GRCh38.p7	9:127454047	CCTCCATGGAACTCA[A/C]TAGAAAGACGCAGCC	90678
rs556546673	snp	G/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127459224	CCTTTGGGGTTTTTT[G/T]TTTTTTTTTTGAGGC	90678
rs556656232	snp	A/C	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127464066	TCCATTCATGGTGGC[A/C]CGCAGTCTGGCCAGC	90678
rs556699821	snp	C/T	0.000798403	0.0199641	downstream-variant-500B	LRSAM1	GRCh38.p7	9:127503889	CCTCACCTTCAAGCC[C/T]GTGCGGTTGTGCAGG	90678
rs556723022	snp	A/G	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127455232	GATCCTTTGGCCTCA[A/G]TATAACGTAGTCTCC	90678
rs556760113	snp	A/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127456092	AGTGAATGATTTTTC[A/G]GCAGAGCATTGCAGC	90678
rs556828856	snp	A/G	1.65111e-05	0.0028732	intron-variant	LRSAM1	GRCh38.p7	9:127461124	CTCCCAAAGTGCTGG[A/G]ATTACAGGCATAAGC	90678
rs556831885	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127491833	TGGATGCCTGGGAGC[C/T]GGGTGTGGCCCAGCA	90678
rs556899375	snp	A/G	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127482386	GACCTCAAGTCATCC[A/G]CCTGCCTCAGGCTCC	90678
rs556912318	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127498345	TAGGCCCCTTCTGGA[C/T]GTTCCTGACCCCCCA	90678
rs556959503	snp	A/C	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127474096	TTGAACTGCTTTTTC[A/C]AGGCCTGCTGTGGCA	90678
rs556992473	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127489035	TGGTTTGACTTAGTA[C/T]CTGTGGAGCTTGTCT	90678
rs557093772	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127500777	ACTTAACAAGCGCTG[C/T]GGCCATCCCTGCAGA	90678
rs557104963	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127461496	CCGTATGGGGAGGAG[A/G]GCAGCTGGGCCCCGA	90678
rs557223224	snp	C/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127487142	TGAGCCACGATCACA[C/G]CACTGCACTCCAGCC	90678
rs557230825	snp	A/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127501227	GGGTTGTCTCTGAAC[A/G]TGTTTTCTCCAGTTC	90678
rs557337536	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127460425	TCCCAGCACCACTGC[C/T]GGCCTGAGGCCTTGG	90678
rs557369393	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127460082	TCGGCTCACTGCAAT[C/T]TCCACCTCCCGGGTT	90678
rs557370942	snp	C/G	0.000399281	0.0141238	downstream-variant-500B	LRSAM1	GRCh38.p7	9:127503740	GGTGATGGCTGCGGC[C/G]TGTGCCTCCATGAGC	90678
rs557373216	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127496851	TCTGGAGGCTGAGGG[A/G]CTGTGGGGCTCGTGT	90678
rs557383422	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127479320	GGGGTGGATTCTCCC[A/G]ACTTCTGTGTCCTAA	90678
rs557383479	snp	A/T			upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451452	GCAGGAAAACGCGGC[A/T]ATCGCGAGAACTGTC	90678
rs557444588	snp	A/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	LRSAM1	GRCh38.p7	9:127454412	AGCAGACCAGCTGCA[A/T]GCTCTGTGTTACTGC	90678
rs557547791	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127490308	CCTTTTTAATTTCCC[C/T]CTTTAATTTCAATTC	90678
rs557712019	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127480117	CCAGTCTGGGTGCTT[C/T]AACTGGCACCAGCGT	90678
rs557713870	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127473577	AAAGAGGTGTAAGGG[A/G]TAGCCAGTACCCATT	90678
rs557760316	snp	A/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127484457	AGCCTCCACCTCCTG[A/G]GCTCAAGCAGTCCTC	90678
rs557852255	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127490833	GCGATGCGAGGGACA[A/G]GAGAACTTGACCAGC	90678
rs557902829	snp	C/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127469711	GCTCGCGCCTGTAAT[C/G]CCAGCACTTTGGGAG	90678
rs558076257	snp	A/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127476955	GTGCTGGGATTACAG[A/G]CATGAGCCACCGCGC	90678
rs558113006	snp	A/G	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127477723	CCACTGCACTCCAGC[A/G]TGGGCAAGAGTGAGA	90678
rs558117380	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127470769	AGACACAAAGGAATA[C/T]GTGCTCTTATCAGTC	90678
rs558220413	snp	C/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127486098	CGGCTAAGCGATGAA[C/G]CACATTCGCTGATTG	90678
rs558221196	snp	A/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127481950	GTTCCAGCTAAAAAA[A/G]AAAAGAAATTCAGAA	90678
rs558260776	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127472697	GAAACCATAAAAGGT[A/G]TCATATGATGTGATT	90678
rs558297566	snp	A/C	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127473249	TACCCCGGAAGGACA[A/C]CATCATCAAAGTTAA	90678
rs558338529	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127466975	GCACTCCAGTCTGGG[C/T]AATGGGAATGAGACC	90678
rs558361694	snp	A/C	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127479039	ATAAAATATTTGAGA[A/C]AATGACTTCTTCCCA	90678
rs558382961	in-del	-/T	0.00676609	0.0577691	intron-variant	LRSAM1	GRCh38.p7	9:127466401	TAGATATCCCTCCAA[-/T]TTTTTTCTATAAAAT	90678
rs558476399	snp	A/C	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127462948	CTCCTGTAATCCCAG[A/C]ACTTTGGGAGGCCAA	90678
rs558498765	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127487366	GAGCTCCCCACCCAT[A/G]GAGGTGGCTGGGCAG	90678
rs558625626	snp	A/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127460459	GATCACACGGCCTTA[A/G]GGCAGCCTTTTCCTT	90678
rs558626068	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127461761	CAGAGCCAAGACCAC[C/T]GCACAGGCGCCTTAC	90678
rs558713532	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	RPL12, LRSAM1	GRCh38.p7	9:127451967	ACTCCGGCTCCGCCC[G/T]GCCCGTGCCGGGTGG	90678
rs558857691	in-del	-/AAAAT	0.00199481	0.0315187	intron-variant	LRSAM1	GRCh38.p7	9:127494878	CAAGAGTCCATCTCA[-/AAAAT]AAAATAAAAGTACCA	90678
rs558871054	snp	A/G/T	0.000181713	0.00953024	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127459051	CTTCCTGACGATCTG[A/G/T]GGCAGCTGACTGCCC	90678
rs558919082	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127464596	TACAGCTCAGAGCAC[A/G]TTCCCAATCCTGAAG	90678
rs558964413	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127471363	GTAGTGCCAGCTGCT[C/T]GGGAGTCTTAGGTGG	90678
rs559053448	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127458534	GCAGTGAGCTGAGGT[C/T]GTGCCACTGCACTCC	90678
rs559142569	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127465240	TCTTTGGCACAGCAA[C/T]GTCCAGTCACTGCTC	90678
rs559219413	snp	A/G	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127485354	CGAGGTCAAGAGATC[A/G]AGACCATCCTGGCTA	90678
rs559221304	snp	C/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127485321	CCAGCACTTTGGGAG[C/G]CCAAGGCGGGTGGAT	90678
rs559272141	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127492550	TTGTCATTTCTTTTG[C/T]TTGATGTTTCTTACC	90678
rs559309350	snp	A/G	0.00199481	0.0315187	intron-variant	LRSAM1	GRCh38.p7	9:127455409	GCTGGCCACATCCCC[A/G]ACACCACTGCTTGCC	90678
rs559310196	snp	G/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127493106	TCACTCTGTCGCCCA[G/T]GCTGGAGTGCAGTGG	90678
rs559349895	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127500819	CTCCCATTCTGCAGA[C/T]GGGAAATGAGGCTCA	90678
rs559383934	snp	G/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127474579	AACTCTATGGGAAAT[G/T]ATCTGTCTCATGTCT	90678
rs559440211	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127494360	CCGTTGTTCTGAGCA[C/T]GGGCTCTGGAGCAAG	90678
rs559472765	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127495103	ATTACAGGCATGTGC[C/T]GCCATGCCTGGCTAG	90678
rs559545921	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127489141	TGTGTGTCCCAGCGC[C/T]GCTGATTCATGCCTC	90678
rs559595077	snp	C/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127481355	CCGCCCAGGTCCAAG[C/G]AATTCCCCTGCCTCA	90678
rs559632704	snp	A/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127475162	AATATTTGCAACACA[A/G]TCACTGGCTGAAGGA	90678
rs559801930	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127500098	GGGCACGTTGGCTCA[C/T]GCCTGTAATCCCAGC	90678
rs559808130	snp	A/C			upstream-variant-2KB, intron-variant	RPL12, LRSAM1	GRCh38.p7	9:127452574	CTTGCATGTGGGTTG[A/C]TTTGTGGCTAACATT	90678
rs559889288	snp	A/C			utr-variant-3-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127503003	CGTATGAGGCTCCCC[A/C]CTGCCCTGGGCCCCT	90678
rs559956603	snp	A/C	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127473657	GGCTAGGACCGGTGA[A/C]AAACACGAAGCGCCC	90678
rs559957552	snp	A/G			intron-variant, utr-variant-5-prime	LRSAM1	GRCh38.p7	9:127454107	GCAGCCCCTGCCCCC[A/G]TGGAACTCACTAGAA	90678
rs560024567	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127477054	CATAGAATTGTTCAC[C/T]AACATTGGGTGAATT	90678
rs560055649	snp	G/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127470861	TCATCAAGCTCTGCA[G/T]GAAGATTCTGTGCTC	90678
rs560113463	snp	A/C			intron-variant	LRSAM1	GRCh38.p7	9:127480517	TGCCCTGCCACTTCC[A/C]GGCCTCTTTTTTCTA	90678
rs560119313	snp	A/G	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127469780	CATCCTGACTAACAC[A/G]GTGAAACCCTGTCTC	90678
rs560177062	in-del	-/CA	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127449551	ACTCTTCAGGAATCC[-/CA]GAGGGTTGCTACCTG	90678
rs560220678	snp	G/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127470347	GTGCCAAGTGAAGAG[G/T]GAAGCCCCTTATAAA	90678
rs560278236	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127492442	TCTGGTTTGCACGCA[C/T]CTCCATTTGTGTGGG	90678
rs560353920	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127463497	CTCCCTCCTTGGCTT[A/G]TAGGTGCTGTCTTCC	90678
rs560354493	snp	A/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127502023	GAGATGCTGAGGCAA[A/T]GTGTGGTCCTGAGTC	90678
rs560392933	snp	A/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127464362	CTAATGAGCACCTGG[A/T]GACCGTGCTGTCCAG	90678
rs560400441	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127489791	GGGCCAGGGAGGCTG[A/G]TGCTGATGTGTGGCT	90678
rs560406093	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127497482	TTCCTCCCAAGGAGC[A/G]GGCTTAGGGATCAGT	90678
rs560424116	snp	A/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127456514	GGGATTACAGGTGTG[A/T]GCCACCACGCCCAGT	90678
rs560469459	snp	A/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127469902	CCCGGGAGGAGGAGC[A/T]TGCAGTGAGCCGAGA	90678
rs560513053	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127465810	GATGAGAGGGCCTGT[A/G]GGAAGTCAGAGGTTG	90678
rs560676962	snp	A/G	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127491933	TCTCCAGCTGCAGAC[A/G]GAGGGCTGGATGGGA	90678
rs560689433	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127460188	ATATTTTAGTAGAGA[C/T]GGGGTTTCACCATGT	90678
rs560754926	snp	C/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127450356	CAACACAGCTGGAAA[C/T]GCTCACTGGATCTTC	90678
rs560777179	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127469416	CAGAGGTTGCAGTGA[A/G]CTGAGATTGTGCCAC	90678
rs560787696	snp	A/C	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127496517	TCAAAACAGAATACT[A/C]ATCGCTGTGCCAGCT	90678
rs560817910	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127488324	TGGAGTGCAGTGGTG[C/T]GATCTCGGCTCACTG	90678
rs560841414	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127491018	CCATGCCCCAGGAAC[A/G]CGAGGCCATGAAGGA	90678
rs560983613	snp	C/T			intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127450368	AAACGCTCACTGGAT[C/T]TTCACCCACACCCCG	90678
rs561076443	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	LRSAM1	GRCh38.p7	9:127453481	GTATTCACCGCAGAG[G/T]TCTCTTTGGTCATGA	90678
rs561143008	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RPL12, LRSAM1	GRCh38.p7	9:127452202	GAAAGAACTGATCTT[C/T]GGGGAGGGGTGGGAG	90678
rs561173572	snp	C/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127497878	ATGAACCACGTTGAG[C/G]AACCTCCGGATCCAT	90678
rs561220926	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127494179	CATCCGGCTCCTGGG[C/T]GCTGGAAGAGAGGGG	90678
rs561316557	snp	C/T	0.000798403	0.0199641	utr-variant-5-prime, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451382	AAGTTGCACCTTGGC[C/T]TCCTCCGAGCCGAAA	90678
rs561352565	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127491967	TGTGTGAGGACATGT[A/G]CCTGTGCCAGGAGTT	90678
rs561381804	snp	C/T	0.00279162	0.0372561	intron-variant	LRSAM1	GRCh38.p7	9:127498931	AGGCGTGGTGGCGTG[C/T]ACCTGTAGTCCCAGA	90678
rs561391862	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127457839	CTTGGGAGAGTGATA[C/T]GCACCTTCAGAGGAG	90678
rs561418774	in-del	-/TTTA	0.00242375	0.0347275	upstream-variant-2KB, intron-variant	RPL12, LRSAM1	GRCh38.p7	9:127453072	CATCTACTTCTTCAC[-/TTTA]TTTATTTATTTATTA	90678
rs561460284	snp	A/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127472278	AAATAATTTTTCAAT[A/T]TACCTAAACTATGTA	90678
rs561759350	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127470181	AGTCTGTTCTCACAC[C/T]GCTATGAAGAAATTC	90678
rs561763149	snp	C/G/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127495599	TGTTCATTCTGGTGA[C/G/T]GGGGACGACAAGGCA	90678
rs561780470	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127481544	TGAGCCACTGCTCCC[A/G]GCCAAGGAGAGCAGC	90678
rs561799978	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127489205	TAAAAGCACCCCCAC[A/G]GTCCACTGTGGTGGA	90678
rs561834372	snp	C/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127469203	ATATCCACACGGTGG[C/G]TCACACCTGTAATCC	90678
rs561952126	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127475786	CACTCTGTTGCCCAG[A/G]CTGGAGTGCAGTGGT	90678
rs562049225	snp	G/T	0.00159617	0.0282053	intron-variant	LRSAM1	GRCh38.p7	9:127501678	CAGAGATTGCAGTGA[G/T]CCAAGATCCCACCAC	90678
rs562052410	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127469833	AGCAAGGCGTGGTGG[C/T]GGGCGCCTGTAGTCC	90678
rs562067746	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127467345	TGCCATCCACTGCGC[A/G]TGTCCCCAGGAGCTG	90678
rs562094537	snp	A/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127477094	AGATTATACTTGATT[A/T]AAAAAATGTTTATAT	90678
rs562212344	snp	C/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127500909	GGCTCCCCCACCCTC[C/G]AGCTCACTCACCATG	90678
rs562256621	in-del	-/A			intron-variant	LRSAM1	GRCh38.p7	9:127480474	GGGGCCCATTGCAGG[-/A]TGATTCCAGAAACAG	90678
rs562273106	snp	G/T	4.4404e-05	0.00471169	intron-variant	LRSAM1	GRCh38.p7	9:127467836	CTCTGCAAAGGTAAA[G/T]CCAGGCCGCTGCCTC	90678
rs562400563	snp	G/T	0.00636936	0.0560724	intron-variant	LRSAM1	GRCh38.p7	9:127469944	CACTCCAGCCTGGGA[G/T]ACAGAGCAAGACTCC	90678
rs562406839	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127497904	TCCATCCCGTGAGGA[A/G]GCACTGTTGTGGTCC	90678
rs562408597	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127455462	CTGCCACCTGCTGTG[A/G]CGTTTTGCCCTTGTT	90678
rs562518477	snp	A/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127464882	TCTTGGGCTCAAGCA[A/G]TCCTCCCGCCTTGAC	90678
rs562544656	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127457224	GCAAGATGGTGGGGC[A/G]TGGCACGGCGCTGGG	90678
rs562602600	snp	A/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127470929	CACAGTCAGTTACAG[A/G]TTTAAGGCCTTGTTC	90678
rs562719381	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127450899	ACGCCACCCTCTGCC[C/T]CTTCTCGAAACAGCA	90678
rs562783995	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127469913	GAGCTTGCAGTGAGC[C/T]GAGATTGCGCCACTG	90678
rs562804223	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127496634	GTACATATCATTATC[A/G]TCATCTTTCAGTTGA	90678
rs562805835	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127492022	TGTCCCTGTGTCTGT[C/T]CTCAGTGGAGAAGTC	90678
rs562817560	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RPL12, LRSAM1	GRCh38.p7	9:127452366	CCCCATCCTTGCAGG[C/G]AGGTGGGGTGACAAG	90678
rs562820752	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127483084	CTGGCAGGGTGGATG[A/G]CCCTCCCTCTGTTGG	90678
rs562854965	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127495047	ACCTCTGCCTCCCGG[A/G]CTCAAGAGATTCTCC	90678
rs562858221	snp	A/C	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127483639	ATATGCATCATGTAA[A/C]CTTTACCATCTTAAT	90678
rs562881246	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127450500	GGCCCACCCCTCAGG[C/T]ACACTAAAGCAGCAG	90678
rs562939032	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127503430	GCCCTCCTGCTCTCC[A/G]CAACTGTCCCTCCTT	90678
rs562957751	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	LRSAM1	GRCh38.p7	9:127454164	TCACTAGAAAGACGC[A/G]GCCCCTGCCTCCGTG	90678
rs562999256	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127471860	TAAAGACAGGGTTTC[A/G]CCATGTTGACCAGGG	90678
rs562999564	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127497087	TCACAGCTATGGTGC[C/T]GCACTGCCTCATCCT	90678
rs563007844	in-del	-/T			intron-variant	LRSAM1	GRCh38.p7	9:127471970	CCCTGCAAGAAATAA[-/T]TTTTTTTTTTTGAGA	90678
rs563016202	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127491074	CGAGGTTCCCAGGCC[C/T]GCAGGTTCCCCTCAT	90678
rs563134858	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127490392	GGGACTTAGGGATGA[A/G]GGTCACAGGGTCATG	90678
rs563244356	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127494235	GAAGGGAGCAGTGGG[C/T]GTGGCCAGGTCCAGG	90678
rs563259174	snp	C/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127480678	CAAATGCACCAAGAA[C/G]CTGGGTTGTTTTCAT	90678
rs563259179	snp	A/G	0.000296487	0.0121719	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127473866	GAGCAAGATGGAATC[A/G]AGAACTCTCGGGACA	90678
rs563289493	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127454943	TTTGCCTGGCTTGTC[C/T]ACTCTGCAAAGGTGT	90678
rs563301753	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127486376	GGTCCGGCTCCCTGT[A/G]CTCACTGGGCACTGT	90678
rs563308364	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127460691	TTTCCTGTCTCCAGC[A/G]GAAACAAGAATTTCT	90678
rs563447915	in-del	-/A	0.0569829	0.158885	intron-variant	LRSAM1	GRCh38.p7	9:127456865	GCAAGAGTTGGTCTC[-/A]AAAAAAAAAAAAAAA	90678
rs563597347	snp	A/G			intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127449513	GGTGAAATCACTCTC[A/G]GCTCACCACTGGTGG	90678
rs563743028	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127484910	CCTCCCGGGTTCAAG[C/T]GATTCTCCTGCCTCA	90678
rs563761880	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127502214	CAGTTTTATTTAAGA[A/G]AGAATCAGTTGGGGC	90678
rs563768733	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127474950	GGAGTACCAGCTGCC[A/G]GGCATTTGGCTTCAT	90678
rs563787317	snp	A/C	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127478772	CCTGGTGCCCTTGAT[A/C]AATACGGATCCCCTC	90678
rs563798105	snp	A/C			intron-variant	LRSAM1	GRCh38.p7	9:127499522	GGTGACAGAGCAAGA[A/C]CCTGTCTAAAAAAAA	90678
rs563824516	snp	A/C	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127479255	TGGGCCCTGGAGGGG[A/C]GTGGGGGTTGCTCAG	90678
rs563842364	in-del	-/AAAAAAAAAAA	0.481856	0.0935034	intron-variant	LRSAM1	GRCh38.p7	9:127500358	GAGCGAGACTGTCTC[-/AAAAAAAAAAA]AAAAAAAAAAAAAAA	90678
rs563967004	snp	A/C			intron-variant	LRSAM1	GRCh38.p7	9:127477477	CCTGTGTGCCAGGCG[A/C]AGTGGCTCACGCCTA	90678
rs564006029	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127465933	ACACGGAGGCATCTG[C/T]ATGTGTGCGCTGATA	90678
rs564042292	snp	A/T	0.000192234	0.00980204	intron-variant	LRSAM1	GRCh38.p7	9:127482904	TGCTGGGATTCCCTG[A/T]TGGAAATGTTAAATT	90678
rs564092596	snp	A/C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127474480	CTGAGAAGCTCCAGT[A/C/T]GAGGTCAGGTCTCCT	90678
rs564163339	snp	C/G/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127464763	ATCCTCCTCCTCAGC[C/G/T]TCCCAAGAGACTGGG	90678
rs564188990	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127482385	TGACCTCAAGTCATC[C/T]GCCTGCCTCAGGCTC	90678
rs564227404	snp	G/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127476356	ATCAACACCAGCCTG[G/T]GCAATGTGGCGAGAC	90678
rs564231332	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127469837	AGGCGTGGTGGCGGG[C/T]GCCTGTAGTCCCAGC	90678
rs564231644	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127475014	ATGCCACCCTTTCCC[A/G]TTTTCCACTGCTGCT	90678
rs564250195	snp	A/C	1.6528e-05	0.00287467	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127501054	ACCCCTACGGCCCCC[A/C]AGGAGCCTCCTGAGT	90678
rs564367805	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127470228	AATTCTTTATAAAGA[A/G]AAGAAGTTTAATTGA	90678
rs564404351	snp	A/G	0.00517822	0.0506191	intron-variant	LRSAM1	GRCh38.p7	9:127502478	TCACTTGGGGTCAGG[A/G]GTTCGAGACTAGCCT	90678
rs564404684	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127495673	GAGCAAAGCCTGTGC[C/T]GGGAGCCACTGTCTG	90678
rs564416295	snp	C/T	0.000798403	0.0199641	downstream-variant-500B	LRSAM1	GRCh38.p7	9:127503554	AGGGAGGGGAGGGGA[C/T]GAGGTCTGGGGATGG	90678
rs564420811	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127467875	ATTGAGGAACTATGA[C/T]CCCCATGGCCACCCT	90678
rs564438459	snp	C/G/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127463302	TGTCTCAGGGAGGGT[C/G/T]GAGGAAGTGATGTGG	90678
rs564444003	snp	A/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127496377	CAGGCCCTTGGGGCT[A/T]ATCTGATCCAGCCTC	90678
rs564631398	snp	A/G	0.00318978	0.0398085	intron-variant	LRSAM1	GRCh38.p7	9:127499092	AAAAACAAATATAGA[A/G]GCTGGGTGCAGTGGC	90678
rs564675432	snp	C/G/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127461699	GAGGAAAACAAGGCC[C/G/T]GGGAAATCAAGTGTG	90678
rs564681115	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127456290	CCAGGCTGGAGTGCA[A/G]TGGTGCAATCTCAGC	90678
rs564786472	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127498747	TTACTCCCAGAAATC[A/G]GTATACTTTATATCA	90678
rs564793870	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127501469	AGGCATGGTGGCTCA[C/T]GCCTGTAATCCCAGC	90678
rs564819547	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127449535	CACTGGTGGCAGAAA[C/T]ACTCTTCAGGAATCC	90678
rs564823725	snp	A/C	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127499376	GACTGTCTCAAAAAC[A/C]AAACAAAAAAATTAA	90678
rs564856028	snp	A/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127493370	CCTAGCCTCTCCTGC[A/G]GTTTTGATGCATATT	90678
rs564902335	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127459311	GCAACCTCTGCCTCC[C/T]GAGTTCAAGCGATTC	90678
rs564944677	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451043	AACGCCCGGAGACAA[A/G]CCTTACCCTAGGGCG	90678
rs565025721	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127458838	TATAATGGTTTGAGA[A/G]GGAAAATGAGGCGGG	90678
rs565035884	snp	A/G	0.00557542	0.0525036	intron-variant	LRSAM1	GRCh38.p7	9:127466573	GCCCAGGCTGGTCTC[A/G]AACTCCTGGGCTGAA	90678
rs565081184	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451372	CGACCGAAGGAAGTT[A/G]CACCTTGGCCTCCTC	90678
rs565104700	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127464311	AAATGTTCAGTGACC[A/G]TGCTGTCCAGAGCGG	90678
rs565180464	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	LRSAM1	GRCh38.p7	9:127503979	TGATTATGCATTTTC[C/T]GGCAGACGGCGTTGA	90678
rs565252654	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127457756	TGTGAGCTCCTCCCC[A/G]GATGGGCTGGGAGGC	90678
rs565307420	snp	C/T	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127502207	TAATCCCCAGTTTTA[C/T]TTAAGAAAGAATCAG	90678
rs565324426	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127497125	GGCCCCGCCAGGCCC[C/T]GGAAGGCTTCCACAT	90678
rs565371492	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127480825	CCCAAGGAGCTGGGA[C/G]TACAGGCTTGGGCCA	90678
rs565383740	in-del	-/ATTAC			intron-variant	LRSAM1	GRCh38.p7	9:127478148	AATTAAACACCAATA[-/ATTAC]ATTACATTATTGATG	90678
rs565398201	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127491124	CCCCAGAAAGGCTTC[C/T]TAGACCCACTTGGTC	90678
rs565419055	snp	G/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127484732	GACTCTTATGAATAA[G/T]GCTACAAATGTGTGT	90678
rs565435563	snp	C/T	0.00159617	0.0282053	intron-variant	LRSAM1	GRCh38.p7	9:127483967	GTGCCTGGTCTTCAT[C/T]TTAAAATATATTAGT	90678
rs565458521	snp	A/G	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127478048	CAAGAGCAAAACTCC[A/G]TCTCAAAAAAAAAAA	90678
rs565506078	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127478778	GCCCTTGATCAATAC[A/G]GATCCCCTCATCCCC	90678
rs565639298	snp	G/T			intron-variant	LRSAM1	GRCh38.p7	9:127481888	TGGCAAAACGCTGTC[G/T]CTACTAAAAATCAAA	90678
rs565668019	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127460912	CCAGGCCGGAGTGCA[A/G]TGGTGCAATCTCAGC	90678
rs565827207	snp	C/G/T	3.29507e-05	0.00405887	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127473897	GCCCTGATGGGCCCA[C/G/T]GGACAGATTCTCAAG	90678
rs565838924	snp	A/G			intron-variant, utr-variant-5-prime	LRSAM1	GRCh38.p7	9:127453775	CTCAATGTTTAGTCA[A/G]CAAAGAACAAGGAGT	90678
rs565955354	snp	A/G	0.00159617	0.0282053	intron-variant	LRSAM1	GRCh38.p7	9:127455426	CACCACTGCTTGCCA[A/G]CCTTGCCCCTGGGCT	90678
rs566023495	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127478803	ATCCCCCGACCCCAC[C/T]ATTCTGAGGCAGTGG	90678
rs566033919	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127471955	AGTGTGAGCCACCAC[A/G]CCCTGCAAGAAATAA	90678
rs566042365	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127499658	AGTTGTGGCCGGGTG[C/T]GGTGCCTCACGCCTG	90678
rs566050905	in-del	-/C	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127475351	CAAAACTTAGCCAGG[-/C]ATGGAGGCGTGCACC	90678
rs566054316	in-del	-/A	0.0248432	0.108648	intron-variant	LRSAM1	GRCh38.p7	9:127465077	AGATCTTCAGGTGTC[-/A]ACGCACGCCACCCAC	90678
rs566181269	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127473067	AAGAGTCTGCTAATC[A/G]GATGGATAACAAGAG	90678
rs566269533	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127460322	TCTATTTTTAATGGT[C/T]AGTGTGTCATCCTGC	90678
rs566289631	snp	A/C			intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127450245	AGGCCTAATGAAATT[A/C]AGAGAAATCCAAGAG	90678
rs566332695	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127499668	GGGTGCGGTGCCTCA[C/T]GCCTGTAATCCCAGC	90678
rs566444295	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127488673	ATCACAGTTCACTGC[A/G]GCCTCAAACTCCTGG	90678
rs566579651	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	LRSAM1	GRCh38.p7	9:127503647	GAGGAGAGGTCAGGT[A/G]GGGCCATCTCGAATG	90678
rs566623718	snp	A/G	1.6531e-05	0.00287493	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127457375	ATCCTGCAGCCTCCT[A/G]AGTCTGGCAACCATC	90678
rs566627238	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127497161	GCAGGAGGTGTCGAC[A/G]GTCCTGTGAGCCTGG	90678
rs566634797	snp	C/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127495793	AGCGGCAGTGAACCC[C/G]TGGGCCTATCTATCT	90678
rs566640282	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127449861	TCACCATAGCATAAA[C/T]TGGGGGTTGGGGTTC	90678
rs566650073	snp	A/C	6.94999e-05	0.0058945	utr-variant-3-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127502936	CTGGTCCTAGCCCTG[A/C]CTCGGCCACTGTGAG	90678
rs566678372	snp	A/C	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127457830	AGACCTGAGCTTGGG[A/C]GAGTGATATGCACCT	90678
rs566686299	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127496801	TCCAAGAGGACTGGA[C/T]GGCACTGAGGGTCAC	90678
rs566783189	snp	C/G	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127490646	CTGAGCCTCAGTTTT[C/G]TTGTCTATAAAATGG	90678
rs566864215	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127455970	TAGAGATAGAAATAT[A/G]CTGAGTGTACATGCC	90678
rs566890772	snp	C/G/T	0.000400781	0.0141513	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127501125	GGCCTCAGAGTGTGT[C/G/T]GTGTGCCTGGAACGG	90678
rs566932341	snp	C/G/T	0.000379945	0.013778	synonymous-codon, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127449670	GCCCTTCCAGTCACC[C/G/T]GTTGCCTTGGCAATG	90678
rs567024645	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127485174	ATATCAAAATGGAAT[A/G]ATATTTCTGGATGAC	90678
rs567075201	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127496604	CTCACTGAATTCTCC[C/T]GACAGCCCAGCAGGG	90678
rs567115765	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127482552	CAGTGTAGGAAAGTG[C/T]CCATTTCTCCACCAC	90678
rs567139235	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127481766	ATATTCCTAGTATAA[A/G]AAGTTCAGGCCAGGC	90678
rs567152132	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RPL12, LRSAM1	GRCh38.p7	9:127452590	TTTGTGGCTAACATT[C/T]ATTGAGCGCTCATGT	90678
rs567162793	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127478492	TGTATGAGTTATTTC[C/T]AGTGTTTTTGCTCTT	90678
rs567163038	snp	C/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127485895	TGGCTCAGGGCCCAA[C/G]ACCGTGGGATGAGAG	90678
rs567176332	snp	C/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127475410	GCACAAGAATCACTT[C/G]AATCCAGGAGGCAGA	90678
rs567199721	snp	A/G	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127478858	AACATCAGGCCACCC[A/G]GGGGTTCCTGGTGCC	90678
rs567241861	snp	C/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127497703	TATACCCAATGCTGG[C/G]CCTGAGGCATGCCTG	90678
rs567386621	snp	A/C			intron-variant	LRSAM1	GRCh38.p7	9:127461364	GAGCAGGAGGGCAGC[A/C]AGTCTCCGGGGGTCG	90678
rs567462703	snp	A/G	0.00438332	0.0466095	intron-variant	LRSAM1	GRCh38.p7	9:127472466	TACCAACATGCGGAA[A/G]CCCTGTCTCTACTAA	90678
rs567514691	in-del	-/A	0.182614	0.240747	intron-variant	LRSAM1	GRCh38.p7	9:127478053	GCAAAACTCCGTCTC[-/A]AAAAAAAAAAAAAAA	90678
rs567645529	snp	C/T	0.00358779	0.0422022	intron-variant	LRSAM1	GRCh38.p7	9:127465142	TGGCTATGAGGAGAC[C/T]ACAGCCCCAGGACAC	90678
rs567677202	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127477575	GTAACATAGCAAGAC[C/T]TTGTCTCTACCAAAA	90678
rs567688044	snp	C/T			upstream-variant-2KB, intron-variant	RPL12, LRSAM1	GRCh38.p7	9:127453380	AGCCACCACACCCGG[C/T]GTGTTTCTTCACTTT	90678
rs567705471	snp	A/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127471201	AAAGATTTTGGGGCC[A/G]AACAAGGTGGCTCAC	90678
rs567711750	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127483255	GCTTACTGCTCCCCA[A/G]CTTTTCCAAGGCTCG	90678
rs567748792	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127484128	CATTCTACTTTCTGT[A/G]TGTGGATTTGAGTGT	90678
rs567892072	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127479829	TCAGGACCCCTACCT[C/T]CGGCTGCAGGAGCAG	90678
rs568040152	snp	A/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127474015	AGCTGGGAATGGAAG[A/G]GGGCGGTGGTTCAGA	90678
rs568048850	snp	A/C	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127456041	AATAGAAACTCACGC[A/C]TTTTATTCTGGTCAC	90678
rs568103134	snp	A/G	0.00159617	0.0282053	intron-variant	LRSAM1	GRCh38.p7	9:127480045	CCTGAGGAGCCGGGA[A/G]GAGTGTGTTTCTCCC	90678
rs568135077	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127502130	AAGCCTGAACACCCT[C/G]CGTGCCCTCCGGCAG	90678
rs568161517	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127474690	GGACCAAATGCTACT[C/T]ACTGTCTGGGACACA	90678
rs568193083	snp	C/G			upstream-variant-2KB, intron-variant, utr-variant-5-prime	RPL12, LRSAM1	GRCh38.p7	9:127452267	CACATCAGGAAGGGG[C/G]TGCAAGAGGGTTAGT	90678
rs568404372	snp	A/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127473089	TAACAAGAGAGCCCA[A/T]TATTATTCTAATGTC	90678
rs568415967	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127493906	AGCTGCGTCCTAGGC[C/T]GGGTCCTGTGCAGGT	90678
rs568528620	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127502989	GTGCCAGCCAGACTC[A/G]TATGAGGCTCCCCCC	90678
rs568554846	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127499712	GAGGCGGGCAGATCA[C/T]GAGGTCAGGAGATGG	90678
rs568565403	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	LRSAM1	GRCh38.p7	9:127503737	GCCGGTGATGGCTGC[A/G]GCCTGTGCCTCCATG	90678
rs568586849	snp	C/T	0.00199481	0.0315187	intron-variant	LRSAM1	GRCh38.p7	9:127493756	ACATTTTCAGCGTGG[C/T]AGAGGCCCCCTTGAG	90678
rs568594435	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127460350	TGCTAGCCTTGCTCA[C/T]CTCGAGGTACCACCT	90678
rs568648029	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127468714	GACATGGTGGCTTGC[A/G]CCTGTAATCCCAGCA	90678
rs568701912	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127494469	GTAGAATCTCCTTCC[C/T]GGAGTTGTGAGAATT	90678
rs568734280	snp	C/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127487049	ATTAGCCAAACGTAG[C/G]AGTGGGCGCCTGTAA	90678
rs568741521	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127497605	CCCATAGCCTTCCCT[C/T]AGTCCACCCTACAGA	90678
rs568770619	snp	G/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127487801	AGGGTGGGAGCTCAG[G/T]AGGGAGGTTCAGGAG	90678
rs568857247	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127463670	CCACATACAGCCACA[C/T]TCTGAGGGATGGGGG	90678
rs568947218	snp	A/T			intron-variant	LRSAM1	GRCh38.p7	9:127456468	ACTCCTGACCTCAAG[A/T]GATCCACCTGCCTTA	90678
rs569010313	snp	A/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127457892	CAGCAGCACAGGCCC[A/T]ATCTGTTATACTATA	90678
rs569047136	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451181	GGAAGGTCTCTGGGA[G/T]GCAGCGGCTTTAAGA	90678
rs569060770	snp	G/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127484349	TTAATAGTAAATAAC[G/T]TTGCATTTCCTGTAT	90678
rs569062299	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127490824	CCTGCAACAGCGATG[C/T]GAGGGACAAGAGAAC	90678
rs569084114	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451405	AGCCGAAAGCCGAGA[A/G]GCCGGAAATCGCGCG	90678
rs569141696	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127483347	AGCGCTTTAGGAAGC[C/T]GAGGCTGGAGGATCA	90678
rs569147241	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127482591	TCACAAACAGTTACC[A/G]GTTTTCTTACTGTCA	90678
rs569149288	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127475547	TTGCTGGTAATCAGA[A/G]GAGAGGCATGTTAAG	90678
rs569245107	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127449821	TCAAGTACCTAAGGG[A/C]ACCTTCTCAATCAGA	90678
rs569253017	snp	A/T	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127489859	GCAGGACTTCCCCAC[A/T]GGGAAAAGCAGCCGG	90678
rs569285087	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	LRSAM1	GRCh38.p7	9:127453570	TGACAGCGTTTGGGG[A/G]GCTAGAAGTGATTCA	90678
rs569417809	snp	C/T	1.64781e-05	0.00287033	intron-variant	LRSAM1	GRCh38.p7	9:127478986	AATGCCTTTACCCTT[C/T]TGTCACTCTTTTCTC	90678
rs569444256	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127490934	TGCACAAGCCTTTAT[C/T]CTGATCCCACTCTAG	90678
rs569541589	in-del	-/G	0.00159617	0.0282053	intron-variant	LRSAM1	GRCh38.p7	9:127489053	GTGGAGCTTGTCTGA[-/G]GAAAATTCTCCATTT	90678
rs569567133	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127461786	CCTTACCCGCAGGAG[C/T]GCTCTGCTCGCCACA	90678
rs569659948	snp	G/T	0.00159617	0.0282053	intron-variant	LRSAM1	GRCh38.p7	9:127499042	AGCCTGGGTGACAAG[G/T]GAAACTCTGTCTCAA	90678
rs569736658	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127486687	GCTTACTAACCGTGA[A/G]GTCTCAGGCAAGTCT	90678
rs570045176	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RPL12, LRSAM1	GRCh38.p7	9:127452752	TCTGCAGTTGTGGGT[A/G]GCAGATTTCGGATTC	90678
rs570143209	snp	A/G	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127478261	CACTCCCGTTGCCTG[A/G]AGGTAGTCATCATTA	90678
rs570154802	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127464580	CTACCATTTTAGACA[A/G]TACAGCTCAGAGCAC	90678
rs570248730	snp	C/T	0.000544649	0.0164933	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127459034	ATAATCAGCTGACAG[C/T]CCTTCCTGACGATCT	90678
rs570258908	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127479350	ACTCCCCCAGGGCCT[A/G]TGCTGACAGTCACCA	90678
rs570395182	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127481693	TTCATTAAAACATAC[A/G]TACACTCCTGAAAAA	90678
rs570445829	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127449917	TTGGCCACAATGTAA[C/G]CTAGACCCCCTCCTA	90678
rs570473685	snp	C/T	0.00159617	0.0282053	intron-variant	LRSAM1	GRCh38.p7	9:127461516	CTGGGCCCCGAGCCT[C/T]AGTCACTCATATTTA	90678
rs570490456	in-del	-/C	0.00636936	0.0560724	intron-variant	LRSAM1	GRCh38.p7	9:127495206	ATCTGCCCACCTTGG[-/C]CCCCCCAAAGTGCTG	90678
rs570547425	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127499810	CTATAGTCCCAGATA[C/T]GCAAGAGGAGAGGCT	90678
rs570555109	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127468407	CAGAAGGAGCTAAAA[C/T]CCGGAGCCAGCACTG	90678
rs570590686	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127494189	CTGGGCGCTGGAAGA[A/G]AGGGGCTGCAGCCCG	90678
rs570621152	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127494681	GGGTGCAGTGGCTCA[C/T]GCCTGTAATCCCAGC	90678
rs570680966	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127469027	TTCCTCAAAAGATAC[C/T]ATTTAGGGAAAGAAA	90678
rs570688892	snp	A/G	3.31131e-05	0.00406884	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127457325	ACACAGGTGCTGATC[A/G]TCCACACGAATCACC	90678
rs570696633	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127502183	TCGCCTGTCCAGAGC[A/G]CAGGAATATAATCCC	90678
rs570732998	snp	A/G	0.00107216	0.0231286	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127502848	ACTGCGCACCTGCCC[A/G]CTGTGCCGCCAGGAC	90678
rs570756845	snp	A/C	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127495208	TCTGCCCACCTTGGC[A/C]CCCCAAAGTGCTGGG	90678
rs570783287	snp	A/C	0.00159617	0.0282053	intron-variant	LRSAM1	GRCh38.p7	9:127467455	TTAAGGGAGGGAGGG[A/C]AGGGGGCTGCAGGTG	90678
rs570872733	snp	A/C			intron-variant, utr-variant-5-prime	LRSAM1	GRCh38.p7	9:127453669	CCCTAGAACAGGAAA[A/C]GGATAATGCCAAGGC	90678
rs570920040	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127460888	TGAGACGGAGTCTCA[C/T]TCTGTTGCCCAGGCC	90678
rs570954827	snp	G/T	6.85272e-05	0.00585311	intron-variant, utr-variant-5-prime	LRSAM1	GRCh38.p7	9:127454478	TCCCCAGTCCCTAAC[G/T]TCTCTCCTGTGCCCC	90678
rs570989650	snp	C/T	0.000148247	0.00860822	intron-variant	LRSAM1	GRCh38.p7	9:127455077	GAGGATAGTGTTGGG[C/T]TGTGAATTGGATCTG	90678
rs571003158	snp	G/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127487863	CCTTCCTAGACAGCA[G/T]GTGGGACCACAGAGG	90678
rs571021162	snp	A/C	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127498013	AGCCACTGGGCTTGC[A/C]TGCCTCCCTGGGGAA	90678
rs571026765	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127455494	ACCTCCTGCCTGTCT[C/T]TTCCTCACGTGAATG	90678
rs571039341	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127480214	TGGACCTGTGGCCTC[A/G]GGCAAATGTTTCCCC	90678
rs571107942	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127488749	CAGGGCCACCATGCC[C/T]AGCTAATTTTTTTTT	90678
rs571143655	snp	A/C	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127481097	GCCCCCAGCCCATTT[A/C]CTAAGCCCCTCTGCA	90678
rs571160354	snp	C/T	0.00398564	0.0444627	intron-variant	LRSAM1	GRCh38.p7	9:127458380	GGCGACAGAGCGAGA[C/T]TTCGTCTCAAAAACA	90678
rs571309854	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127477845	CTGAGGTCAGGAGTT[C/T]GAGACCAGCTTGGCC	90678
rs571406961	snp	A/C	0.00636936	0.0560724	upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451435	GGACAAGCCAGATAT[A/C]GGCAGGAAAACGCGG	90678
rs571426958	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127476120	GATAAATGCTTGCAT[A/G]AGGAGACATTTGCAG	90678
rs571435677	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127485008	AGACACAGTTTCGCC[A/G]TGTTGGCCAGGCTGG	90678
rs571464285	snp	C/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127484496	GCCTCCCAAGTAGTG[C/G]GGACTACAGACACAT	90678
rs571465507	snp	C/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127476659	CATGAGCGAATTTTC[C/G]AGGGTGATGGAATTG	90678
rs571472834	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127478437	TGTGTAATAGTCCAC[C/T]GTATGGATGCACCAT	90678
rs571600509	snp	A/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127470517	GCCAGACCATATCAA[A/T]GCCCAATGGAAATGC	90678
rs571663284	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127501458	ATCTTTTGGCCAGGC[A/G]TGGTGGCTCACGCCT	90678
rs571668638	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127483202	TGGATGCAGAGTCCC[A/G]GTTCAAACACCCACC	90678
rs571697813	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127482704	GAATTTCAGCATTGG[C/T]TATTTGCTTCTTTTG	90678
rs571725087	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127498939	TGGCGTGCACCTGTA[A/G]TCCCAGACTCAGGAG	90678
rs571753393	snp	A/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127490438	AGTACTGGCTATGGG[A/G]TCTGACCCCCACCCC	90678
rs571849035	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127474853	GCCACATTAGCCTGC[A/G]TGCCCCCTCTGCCGC	90678
rs571860487	snp	A/G	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127475454	TGAGATTGCGCCACT[A/G]CACTCCAGCCTGTCC	90678
rs571866150	snp	A/G	0.00676609	0.0577691	intron-variant	LRSAM1	GRCh38.p7	9:127460145	GCTGGAATTACAGGC[A/G]CCCACCACTATGCCT	90678
rs571925919	snp	C/T	2.49853e-05	0.00353441	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127489467	GCAGAAGGCTGCGTT[C/T]GAGGCACTCCAGGTG	90678
rs571937856	snp	A/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127463868	GTATCGTCACAGAAC[A/T]CTTGTGAGGCAGATA	90678
rs571998564	snp	C/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127460480	CCTTTTCCTTAAGGC[C/G]AGGGGAACTAGAGCC	90678
rs572162810	snp	A/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127499390	CAAAACAAAAAAATT[A/T]AAAAAAATTAGCAAG	90678
rs572200220	snp	A/G	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127485945	CCCTGGGCCACCCCA[A/G]CCTCTGCTCTGCTGT	90678
rs572257342	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127499873	GAGGTTGCAGTGAGC[C/T]GAGATCGCACCACAC	90678
rs572330792	snp	A/G	0.000133878	0.00818052	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127454533	AAAGGGAAGGATGCC[A/G]CTCTTCTTCCGGAAG	90678
rs572440560	snp	C/T	0.00159617	0.0282053	intron-variant	LRSAM1	GRCh38.p7	9:127458589	TGTCTCAAAATAAAA[C/T]AAAATAAAATAAAAT	90678
rs572479235	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	RPL12, LRSAM1	GRCh38.p7	9:127451968	CTCCGGCTCCGCCCG[A/G]CCCGTGCCGGGTGGT	90678
rs572624291	snp	C/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127485375	ATCCTGGCTAACACA[C/G]TGAAACCCTGTCTCT	90678
rs572675446	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127491940	CTGCAGACGGAGGGC[C/T]GGATGGGATGGTGTG	90678
rs572713754	snp	A/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127492620	TAACCCCACAAGGAA[A/G]AGAGATGCGGGCTTA	90678
rs572804990	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127502312	CTAGGTTACCTGTTT[C/T]GGCCGTGCCTGTTCT	90678
rs572826037	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127461578	GAGCTCCTAAGGAGC[C/T]GCAGTAAGGTTCTGA	90678
rs572847246	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127495569	CCAGTGGAGACAGAA[A/G]CGAGAGTAAGGGAGT	90678
rs572878253	snp	A/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127456881	AAAAAAAAAAAAAAA[A/G]AAAAGGAAAAATAGC	90678
rs572884257	snp	G/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127456229	TGGCGCTGGAAGTTT[G/T]GTTTGTTTTTTTTTT	90678
rs572891810	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127494109	GTGCCCCTGCCCTTG[C/T]AGGCCTTGGGGGTCA	90678
rs572914792	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127450059	GGATGGAGGTCTGAT[G/T]ATTTGCTACTCTGAA	90678
rs572942317	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127496218	CCTAATGGCCCAGGG[C/T]CACCTTGCTTCCAGA	90678
rs573175583	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127482780	ACTACAGGCTGAAGG[C/T]GAACAGAGGGCCCCA	90678
rs573290881	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127491013	CACGTCCATGCCCCA[A/G]GAACGCGAGGCCATG	90678
rs573297700	snp	A/G	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127480324	GGTTCTGCGTAACCC[A/G]TTGCACTGAGGTCAG	90678
rs573327552	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127491824	GTCCTGGACTGGATG[C/T]CTGGGAGCCGGGTGT	90678
rs573366698	snp	C/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127484604	GGCTCAAGCAGTCCT[C/G]CCACCTTGGCCTCCC	90678
rs573418919	in-del	-/TTTA	0.0248727	0.108709	upstream-variant-2KB, intron-variant	RPL12, LRSAM1	GRCh38.p7	9:127453075	TACTTCTTCACTTTA[-/TTTA]TTTATTTATTTATTA	90678
rs573429995	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127480623	TTGGATGCTTCTTAT[A/G]TGCCAAGCTTGTTAC	90678
rs573445158	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127474793	TGTCAGGTCCTGGCG[A/G]CAAGCTAGCACAGGA	90678
rs573783360	in-del	-/C	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127498353	TCTGGATGTTCCTGA[-/C]CCCCCCAGCTCTCAG	90678
rs573800234	snp	C/T	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127462737	TGCTGGGCTTCAAAC[C/T]TGGGTGATGGGACGA	90678
rs573820262	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127463131	TTGAACCCGGGAGGC[A/G]GAGATTGCAGTGAGC	90678
rs573848615	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127464016	CGCCTGTGCTCCCCA[C/T]CTCTGTATGACTCGG	90678
rs573856964	snp	A/C	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127457574	GTGGGTTAGGGTGAC[A/C]AAGATGACCAGCCAC	90678
rs573866612	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127472016	GCCCAGGCTGGAGTG[C/T]GGTGGCGCAATCTTG	90678
rs573985085	snp	A/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127458082	TTTTTGTGCATTTTC[A/G]TTTTTAAAAAATTAG	90678
rs574008395	snp	A/T	0.00199481	0.0315187	intron-variant	LRSAM1	GRCh38.p7	9:127465376	GGACTCAAACTTTAA[A/T]TCAGATTTATTTTCA	90678
rs574037519	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127470132	CAAATATCCTATGGC[C/T]CATGAGTTCCATTCC	90678
rs574196183	snp	A/C	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127497024	GCCTCAGTTTCCCCC[A/C]AACCCCTGCCACACT	90678
rs574202204	snp	G/T	4.97946e-05	0.00498947	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127497299	AGATCCTCCGGAGAG[G/T]CCAGGAACTGCTGGA	90678
rs574216135	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127460585	GAGCATTTTGTGGTC[A/G]GTGTAAGTGCTGGAA	90678
rs574253012	snp	C/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127461062	GATTTCACTATGTTG[C/G]CCAGGCTGGTCTTGA	90678
rs574272190	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127450878	AGCGTCTTTCCGGGG[C/T]TGGACACGCCACCCT	90678
rs574279325	snp	A/G	0.000188671	0.00971082	utr-variant-5-prime, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451321	CTTCGGCGGCATGGT[A/G]GAGGCGGCTGGTGTC	90678
rs574341084	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127494602	ACTGCTGTATTCCCA[A/G]CACCTAGAACAGTAC	90678
rs574458590	snp	C/T	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127467072	ACACTTTGAGACAAA[C/T]TGAGGAGTCCTTTAT	90678
rs574563607	snp	C/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127494204	GAGGGGCTGCAGCCC[C/G]GGAGGGCCAACGACG	90678
rs574622860	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127469822	CAAAAAAAATTAGCA[A/G]GGCGTGGTGGCGGGC	90678
rs574662769	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127499930	CTCCATCTCAAAAAA[A/G]AAAAGAAAAACTTTA	90678
rs574699485	snp	A/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127500750	CCGGGGACATTAGAG[A/T]TCAGAGGACCCACTT	90678
rs574753076	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127498610	GCCACATGCAGAAAA[C/T]GGATGCCTGGGCTGC	90678
rs574793937	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127492678	CTTTGTCCCCCAACG[C/T]AGCCTGGAGGCATTG	90678
rs574826112	snp	C/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127499200	CGACATAGGGAGACC[C/G]CTTCTCTACAAAAAA	90678
rs574835167	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RPL12, LRSAM1	GRCh38.p7	9:127453270	TATTTTTAGTAGAGA[C/T]GGGGTTTGACCATGT	90678
rs574844986	snp	A/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127459172	CCAGCCAGTGGAAGC[A/T]GGCTGCAATCAGTGC	90678
rs574970354	snp	C/T	0.00159617	0.0282053	intron-variant	LRSAM1	GRCh38.p7	9:127493190	CCTCAGCTTCCCGAG[C/T]AGCTGGGACTACAGG	90678
rs575022132	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	LRSAM1	GRCh38.p7	9:127453748	CTTGTCTGTCTCCAC[C/T]TCATCCTGCTGCTCA	90678
rs575034904	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127472773	TCCTGTCTCATAGTA[C/T]GGTTTGAATGTCCCC	90678
rs575152064	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127479160	GGACAGGTGCAGAGA[C/T]TGAGGCTCAGAGGGG	90678
rs575211972	snp	A/G	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127496313	AAATCCTGGGGAGGT[A/G]GGTCCTGCTGACCTG	90678
rs575213071	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127479747	AGGATTGGCAAGGCA[A/G]GGTGGGAAAGCCAGC	90678
rs575264008	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127480494	TCCAGAAACAGGCTC[C/T]AGCCATATGCCCTGC	90678
rs575338700	snp	A/G	0	0	intron-variant	LRSAM1	GRCh38.p7	9:127490203	TGCATCATGTTCAGC[A/G]CACTGAATTTTGCAT	90678
rs575353247	in-del	-/A	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127482098	ACATATTGCTAATGG[-/A]AAAAGTGACAGGCTA	90678
rs575433945	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127491952	GGCTGGATGGGATGG[C/T]GTGTGAGGACATGTG	90678
rs575482891	snp	A/T			intron-variant	LRSAM1	GRCh38.p7	9:127467940	AATGGCCACAGTGCC[A/T]ACCTGCTTGGAGTTC	90678
rs575493186	snp	A/G	0.00557542	0.0525036	intron-variant	LRSAM1	GRCh38.p7	9:127501682	GATTGCAGTGAGCCA[A/G]GATCCCACCACTGCA	90678
rs575502037	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127482211	GCAGTGGCACGATCT[C/T]GGCTCACTGCAACCT	90678
rs575540788	snp	A/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127482874	GAGGCCTTCCTGGAG[A/G]AGGTGGTGTTCATCT	90678
rs575580174	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127488942	CCTCCCTTCTTCCCT[C/T]GCCTTTCTCCCCTGT	90678
rs575614628	snp	G/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127476855	AAGTTTTGCATTTTG[G/T]TAGTAGAGACGGGGT	90678
rs575677021	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127478039	CCTGGGCAACAAGAG[C/T]AAAACTCCGTCTCAA	90678
rs575678736	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127483394	CAAGGCTGCAGTGAG[C/G]TGTGATCACACTACT	90678
rs575699800	snp	A/G	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127478624	GGCATCAGATATCCC[A/G]TTTCCTGCTCTGCTC	90678
rs575713778	snp	A/C	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127471586	GAGGTCGGGAGTTCG[A/C]GACCAGCCTGACCAA	90678
rs575723153	snp	G/T			intron-variant	LRSAM1	GRCh38.p7	9:127485412	AATACAAAAAATTAG[G/T]CGGGCGTGGTGGCAG	90678
rs575739060	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127472118	AGGCGCCCACCACCA[C/T]GCCTGGCTAATTTTT	90678
rs575832535	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127469671	AACCAGAAATAAAAA[A/G]ACAAAAAATAGGCCG	90678
rs575841254	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127468800	GCAACATGGTGAAAC[C/T]CTGTCTCTACAAAAA	90678
rs575994840	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127464381	CGTGCTGTCCAGAGC[A/G]GCGGCCACTGGCCAC	90678
rs576041389	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127484023	GCCACCACCATCCAT[C/T]GCCAGAACTTTTTCA	90678
rs576074053	snp	C/T	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127500453	AGAGCAGCCAGCATG[C/T]TGGGGACTCTGTGGG	90678
rs576147411	snp	A/C	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127458151	TTTGGGAGGCCAAGG[A/C]GGGTGGGTCACTTGA	90678
rs576186580	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127458423	ACAAAACAAAACAAA[A/G]AAAAACACCAGCAGA	90678
rs576186607	snp	A/G	8.7124e-05	0.00659957	utr-variant-5-prime, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451362	GGATTCGGGACGACC[A/G]AAGGAAGTTGCACCT	90678
rs576202058	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127465555	TTTCTGCTGTTGGGC[C/T]CTCAGCATCTGGGCG	90678
rs576269423	snp	A/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127466186	TGGTGGCGCATGCCT[A/G]TAGTTCCAGCTACTC	90678
rs576322986	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant, utr-variant-5-prime	RPL12, LRSAM1	GRCh38.p7	9:127451903	GGTCTGCGTGACTTT[A/G]TGAGATTCTGAGTTT	90678
rs576332029	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127466963	GTTCGTGCCACTGCA[C/T]TCCAGTCTGGGCAAT	90678
rs576404812	snp	A/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127470676	GTGTGGATACCACAC[A/G]GCAAGTGGAAAGAAT	90678
rs576426409	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RPL12, LRSAM1	GRCh38.p7	9:127453357	AAAGTGCTGGGATTA[C/T]AGGCATGAGCCACCA	90678
rs576427643	snp	C/T	0.00199481	0.0315187	intron-variant	LRSAM1	GRCh38.p7	9:127463233	AAAATTCTGAGCAGA[C/T]CTGGATAACAGGGGC	90678
rs576436764	snp	C/T			utr-variant-3-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127503459	TTACCCCATGTAGCT[C/T]GATCCGAAGCAGGAG	90678
rs576540111	in-del	-/A	0.00438332	0.0466095	intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127450050	CATCTTCCTGGATGG[-/A]GGTCTGATTATTTGC	90678
rs576630412	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127491873	TGTGCAACTTTGGCA[A/G]GTGGGGGAGGAGAGG	90678
rs576671521	snp	C/T	0.00716266	0.059414	intron-variant	LRSAM1	GRCh38.p7	9:127484657	AGCCGCCATGTCCAG[C/T]GTCTACATTTTCTTT	90678
rs576720473	snp	A/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127460726	TCCTCAAGGGCCGGT[A/T]GGGGGAGATAAGAGC	90678
rs576722049	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127497597	CTCCCTGTCCCATAG[C/T]CTTCCCTCAGTCCAC	90678
rs576826783	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127499288	CAAAGGTGGGAGGAT[C/T]GCTTGAGCTTGGGAG	90678
rs576864440	snp	A/G	9.90802e-05	0.00703778	intron-variant	LRSAM1	GRCh38.p7	9:127461136	TGGGATTACAGGCAT[A/G]AGCCACTGCGCCTGG	90678
rs576907217	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127466400	ATAGATATCCCTCCA[A/G]TTTTTTTCTATAAAA	90678
rs576931796	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127463003	GAGTTCGAGACCAGC[C/G]TGGCCAACATGGTGA	90678
rs576939610	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127498534	CTCACTGTTTGAGTC[A/G]TCCCTGGAGCAAACA	90678
rs576999801	snp	C/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127488481	TGGCCAGGCTGGTCT[C/G]GAACTCCTGACCTCA	90678
rs577083541	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127469940	ACTGCACTCCAGCCT[A/G]GGATACAGAGCAAGA	90678
rs577111585	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127501321	CCCAAATATGAGCTG[C/T]GCTCACATCATTTTC	90678
rs577111706	snp	C/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127495042	CTGCAACCTCTGCCT[C/G]CCGGGCTCAAGAGAT	90678
rs577217372	snp	A/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127496863	GGGACTGTGGGGCTC[A/G]TGTGCTGCTGCTGCT	90678
rs577235408	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127486365	GGCTGCTCTGGGGTC[C/T]GGCTCCCTGTGCTCA	90678
rs577254396	snp	C/T	9.95867e-05	0.00705574	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127497258	ACTGTCACAGGTGGG[C/T]GTCTCAGAAGCTGGC	90678
rs577269456	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	LRSAM1	GRCh38.p7	9:127453951	ATGAAACTAGGAAGA[C/T]GCAGTCCCTGGCTCC	90678
rs577293265	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127490959	CTCTAGGAGAGATCC[C/T]GTGCTGGCCTCTTGG	90678
rs577314075	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	LRSAM1	GRCh38.p7	9:127454034	GACACAGCCCCTGCC[C/T]CCATGGAACTCAATA	90678
rs577328150	snp	G/T			upstream-variant-2KB, intron-variant, utr-variant-5-prime	RPL12, LRSAM1	GRCh38.p7	9:127451691	GTCACCCCGGTCCCC[G/T]TCACCCAATCCCAGA	90678
rs577631721	snp	C/T	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127474143	TTGCCAAGCACAAGC[C/T]GTGCCCTGCTGCTGT	90678
rs577641977	in-del	-/G			intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127450846	TGCAGAGGGAGCCCC[-/G]GAGCCACAGCCCTCT	90678
rs577678779	snp	A/T	8.15761e-05	0.00638603	intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127450828	AAAGAAGAGTTAGTG[A/T]CTGTGCAGAGGGAGC	90678
rs577694639	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127468892	TACTTGGGAGGCTGA[A/G]GTGGAAGGATCATTT	90678
rs577877185	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127496488	TCTTTACAGCACATT[A/G]ATCCACTTATTCTTC	90678
rs578010232	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127464340	GGCAGCCACTGGCCA[C/T]GTGTATCTAATGAGC	90678
rs578010621	snp	G/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127471386	TTAGGTGGGAGGATT[G/T]CTTGAGCCTAAGAAG	90678
rs578139571	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127502482	TTGGGGTCAGGAGTT[C/T]GAGACTAGCCTGACC	90678
rs578151441	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127503135	CTGGGGCTGGAGAGG[C/T]CGCTGCACCACCACC	90678
rs578257462	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127450298	CAGTTGCTCAGCAGG[A/C]ATGAGACACAGCCTG	90678
rs745307512	snp	A/G	1.64749e-05	0.00287005	intron-variant	LRSAM1	GRCh38.p7	9:127455542	TAAAAACTGGCAGGA[A/G]GGGAGACACTTACTC	90678
rs745314322	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127467182	GTCTAAATAGGGGAG[A/G]GGGGAGTTTAGCTGA	90678
rs745326217	snp	A/G	5.40132e-05	0.00519651	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127467806	GGTGCCGGCACTGCG[A/G]CCATCTTGCAGTTCC	90678
rs745370953	snp	C/T			upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	RPL12, LRSAM1	GRCh38.p7	9:127452055	ACCCGCGGGTCCCAA[C/T]GTGGGGGATCCCTCC	90678
rs745378163	snp	A/G	1.70513e-05	0.00291982	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127496003	GTGGCCCTCCTGGAG[A/G]AGCTGTCGGCTGAGC	90678
rs745423225	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127455992	GTACATGCCTACCAC[A/G]TAGTAAAGGCTTATG	90678
rs745468484	snp	A/T	8.50449e-05	0.00652037	utr-variant-3-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127502950	GCCTCGGCCACTGTG[A/T]GCCCCGGGCTCCTGC	90678
rs745509451	snp	G/T			intron-variant	LRSAM1	GRCh38.p7	9:127470465	CCGCCCCCAACACGT[G/T]GGGATTACAATTCAG	90678
rs745534019	in-del	-/TATA			intron-variant	LRSAM1	GRCh38.p7	9:127472298	TAAACTATGTAGAAG[-/TATA]TATATATATATATGT	90678
rs745561169	snp	C/T	1.65195e-05	0.00287393	intron-variant	LRSAM1	GRCh38.p7	9:127479986	AATCAGAGGTTGGGC[C/T]CTGCTCCTCGGCCCC	90678
rs745571693	snp	A/G	1.72317e-05	0.00293523	utr-variant-5-prime, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451338	AGGCGGCTGGTGTCG[A/G]ATGAACCCGGATTCG	90678
rs745597527	snp	A/T			intron-variant	LRSAM1	GRCh38.p7	9:127469797	TGAAACCCTGTCTCT[A/T]CTAAAAATACAAAAA	90678
rs745601002	snp	A/C	3.40443e-05	0.00412565	intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451274	CGGCCACAACCAGAG[A/C]ACGCACCGACTTTGA	90678
rs745608300	in-del	-/T			intron-variant	LRSAM1	GRCh38.p7	9:127483325	CGGGGCTCATGCCTG[-/T]AATCCCAGCGCTTTA	90678
rs745635872	in-del	-/T/TT/TTT	0.513865	0.0677654	intron-variant	LRSAM1	GRCh38.p7	9:127481255	CAGGGGAGGGCAGCA[-/T/TT/TTT]TTTTTTTTTTTTTTT	90678
rs745672498	snp	C/T	1.65433e-05	0.002876	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127501013	TGGTCCCCACAGAGC[C/T]GAAACCACCAATGGG	90678
rs745687258	in-del	-/T	6.59141e-05	0.00574045	intron-variant	LRSAM1	GRCh38.p7	9:127473781	TCCCTCCTGGTCAGC[-/T]TGTGTCCCGTCTCTT	90678
rs745687638	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127483365	GGCTGGAGGATCACA[C/T]GAGCCCAGGAGTTCA	90678
rs745690669	snp	C/T	0.000573664	0.0169264	intron-variant	LRSAM1	GRCh38.p7	9:127489524	CAGGAGCCAGGTGAG[C/T]GCTGGGGCTGGGGTC	90678
rs745790728	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127495781	GTTTGCAGACAGAGC[A/G]GCAGTGAACCCCTGG	90678
rs745801524	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127481692	GTTCATTAAAACATA[C/T]GTACACTCCTGAAAA	90678
rs745831448	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127462563	ACTTTTGCTGCCATA[A/G]TAGAGGCAGAAAAAC	90678
rs745839330	snp	A/C	1.65184e-05	0.00287384	intron-variant	LRSAM1	GRCh38.p7	9:127458962	CCCGGAGTCTGAGGG[A/C]CTTTCTCACTTGGAG	90678
rs745860051	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127473962	CTGCTGCACGCATAC[A/G]TGTGTGTGTGTGCGT	90678
rs745934945	snp	A/G	3.30147e-05	0.00406279	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127485746	CACAGCCGCCATGCA[A/G]CAGATGCTGACTGAG	90678
rs745956191	snp	C/G	2.72885e-05	0.00369371	intron-variant	LRSAM1	GRCh38.p7	9:127483072	CTGCTGGCTGGGCTG[C/G]CAGGGTGGATGGCCC	90678
rs746042227	snp	C/T	1.71284e-05	0.00292642	intron-variant	LRSAM1	GRCh38.p7	9:127495282	TACAGGTTTTATTAC[C/T]ATTTTGTGACTAACA	90678
rs746055151	snp	A/C	1.64885e-05	0.00287123	intron-variant	LRSAM1	GRCh38.p7	9:127454984	TACTTTTTAAAAATT[A/C]TTTTTATCCTTAGGC	90678
rs746159728	snp	C/T	8.23662e-05	0.00641688	stop-gained, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127462362	ATGCTGGCTCACGTT[C/T]GAACCCTGGAGGTAA	90678
rs746177578	snp	G/T			intron-variant	LRSAM1	GRCh38.p7	9:127501695	CAAGATCCCACCACT[G/T]CACTCCAGCCTGGCA	90678
rs746202048	snp	A/G	1.68343e-05	0.00290118	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127492870	CAAAGAGAAGCAGCA[A/G]CGAGAGGAAGAGCTC	90678
rs746213887	snp	C/T	2.22215e-05	0.0033332	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127502855	ACCTGCCCGCTGTGC[C/T]GCCAGGACATCGCCC	90678
rs746259267	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127499702	TTGGGAAGCCGAGGC[A/G]GGCAGATCACGAGGT	90678
rs746274685	snp	C/G	5.79106e-05	0.0053807	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127467815	ACTGCGGCCATCTTG[C/G]AGTTCCTCTGCAAAG	90678
rs746435196	in-del	-/TCAG	1.65759e-05	0.00287883	intron-variant	LRSAM1	GRCh38.p7	9:127500984	GGAGATGACCCTGGC[-/TCAG]TCTGTCTGTCTGGTC	90678
rs746441464	snp	C/T	1.7309e-05	0.0029418	intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127449759	GAGGTGAACCACAGC[C/T]TTGAAACCTGCCCAC	90678
rs746455518	snp	C/T	1.65143e-05	0.00287348	splice-donor-variant	LRSAM1	GRCh38.p7	9:127479980	CAGGACAATCAGAGG[C/T]TGGGCTCTGCTCCTC	90678
rs746462182	snp	A/C			intron-variant	LRSAM1	GRCh38.p7	9:127470455	CCACGAGTTCCCGCC[A/C]CCAACACGTGGGGAT	90678
rs746516353	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127478325	TCAATACCTTCACAC[A/G]TATGCTCAGAGTTGA	90678
rs746549530	snp	C/G/T	0.000135679	0.00823546	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127479902	AACGCAGAGCGGCAG[C/G/T]GGCTGCAGGAGCAGC	90678
rs746561242	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127502229	AAGAATCAGTTGGGG[C/T]ATTTATATGGGTATT	90678
rs746632020	in-del	-/CTT			intron-variant	LRSAM1	GRCh38.p7	9:127465013	GCACCTCGGACAAAC[-/CTT]CTTTTAGGATGAGAT	90678
rs746664653	snp	A/G			upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	RPL12, LRSAM1	GRCh38.p7	9:127451562	AGGGCACCGCGGTGC[A/G]CTGAAGCTAGAGATT	90678
rs746714138	snp	G/T	3.3e-05	0.00406189	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127459011	TCTGCAGGTTCTAGA[G/T]CTCCACGATAATCAG	90678
rs746714269	snp	A/C/G/T	9.32736e-05	0.00682862	intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127450841	TGTCTGTGCAGAGGG[A/C/G/T]GCCCCGAGCCACAGC	90678
rs746749926	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127495707	AGCACCTGCGGGGAC[A/G]GAGAGGCAGTTGAAA	90678
rs746762801	in-del	-/CAACATGGTGTCCAGA	1.6842e-05	0.00290184	intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127449730	ATAAAGGCATGTAAT[-/CAACATGGTGTCCAGA]GGTGAACCACAGCCT	90678
rs746774733	snp	C/T	1.69309e-05	0.0029095	intron-variant	LRSAM1	GRCh38.p7	9:127497354	AAGCACAGCTCCAGC[C/T]TCTTCCAGGCAGGGC	90678
rs746831085	snp	A/G	6.63812e-05	0.00576075	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127497259	CTGTCACAGGTGGGC[A/G]TCTCAGAAGCTGGCC	90678
rs746894546	in-del	-/A	1.65096e-05	0.00287306	intron-variant	LRSAM1	GRCh38.p7	9:127461130	AAGTGCTGGGATTAC[-/A]GGCATAAGCCACTGC	90678
rs746930955	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127459923	GGATACCTGACAATA[A/G]CTCATAGCATCCTTT	90678
rs746932979	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127475278	GGTGGATCACTTGAG[A/G]CCAGGAGTTTGAGAC	90678
rs746999697	snp	A/C	1.66913e-05	0.00288883	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127454555	TTCCGGAAGCGGAAA[A/C]CCAGTGAGGAGGCTC	90678
rs747044588	snp	A/G	1.90054e-05	0.00308259	intron-variant	LRSAM1	GRCh38.p7	9:127482934	TTGCTGAATGAATGG[A/G]TGGATTTTTTTCTAG	90678
rs747083828	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127488563	CACCGTGCCCAGCCT[A/G]TTTAGCTTTTTATTT	90678
rs747087615	snp	C/T	4.94629e-05	0.00497283	intron-variant	LRSAM1	GRCh38.p7	9:127462244	CTGTGCTATTGGGGT[C/T]TCTGCAGACAACAAG	90678
rs747093644	in-del	-/TG	6.00577e-05	0.00547953	intron-variant, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127487662	AATGAATGAATTTGC[-/TG]TCTTTCTGGCAGCAT	90678
rs747094831	snp	C/T	1.68633e-05	0.00290368	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127492841	GCCCTCAGCTCCCTG[C/T]TCCAGCAGCTGCTCA	90678
rs747130246	in-del	-/A	1.68977e-05	0.00290665	frameshift-variant, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127496080	GAGCCAAATGAGCCC[-/A]GGGGACCTGGCCAAG	90678
rs747142126	snp	C/T	1.70942e-05	0.00292349	intron-variant, utr-variant-5-prime	LRSAM1	GRCh38.p7	9:127454492	CTTCTCTCCTGTGCC[C/T]CAGGGTCCTAAAGAT	90678
rs747184869	snp	A/G	1.83078e-05	0.00302549	intron-variant	LRSAM1	GRCh38.p7	9:127501184	CCTGCCCTGCCTGTG[A/G]CCACCCTCCTCAAAT	90678
rs747224064	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127487045	AACAATTAGCCAAAC[A/G]TAGCAGTGGGCGCCT	90678
rs747245980	snp	C/T			intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127450963	GGGTGTGGGCAGCTC[C/T]GAAACTCACACCGGG	90678
rs747248033	in-del	-/CCT			intron-variant	LRSAM1	GRCh38.p7	9:127459677	ATTCTCATGCCTCAG[-/CCT]CCTCCTGAGTATCTG	90678
rs747301679	snp	A/C	3.29685e-05	0.00405995	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127461254	CAGACTCTCAATGTT[A/C]AAGGTAGGGACCAAG	90678
rs747333236	snp	A/G			utr-variant-5-prime, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451406	GCCGAAAGCCGAGAG[A/G]CCGGAAATCGCGCGG	90678
rs747342170	snp	A/T	3.32884e-05	0.00407959	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127501118	AGGTGCAGGCCTCAG[A/T]GTGTGTCGTGTGCCT	90678
rs747348907	snp	A/G	1.6834e-05	0.00290116	intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127449728	AAATAAAGGCATGTA[A/G]TCAACATGGTGTCCA	90678
rs747368361	snp	C/T	4.99646e-05	0.00499798	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127479495	ATGAGATCCTTCAGA[C/T]GGTCAAGGAGGTTTG	90678
rs747382100	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127465045	TAACCGTTCTGAGTT[C/G]AGGCCGTACTGTGGG	90678
rs747384782	snp	A/G	5.48672e-05	0.00523742	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127487740	ATGGATCAGAACAAA[A/G]CCATCAGCCAGATCC	90678
rs747405179	snp	C/T	1.64931e-05	0.00287163	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127479404	AAGATGCTGGAGAAA[C/T]TCGAGTTTGAACGGC	90678
rs747426963	snp	A/G	1.692e-05	0.00290856	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127496083	CCAAATGAGCCCAGG[A/G]GACCTGGCCAAGGTG	90678
rs747443125	snp	A/G	1.6537e-05	0.00287545	synonymous-codon, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127449622	TACCTGGGCCTGTCT[A/G]TTCTGAATGGTCAGT	90678
rs747457865	in-del	-/TAT			intron-variant	LRSAM1	GRCh38.p7	9:127499541	GTCTAAAAAAAAATA[-/TAT]ATATATATATATATG	90678
rs747458729	snp	A/C			missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127479884	GAGCACCAGCGCCAC[A/C]TCAACGCAGAGCGGC	90678
rs747640905	snp	C/T	2.42404e-05	0.00348132	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127489481	TCGAGGCACTCCAGG[C/T]GAAGAAAGACCTGAT	90678
rs747648840	snp	A/G	5.53868e-05	0.00526216	intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127450835	AGTTAGTGTCTGTGC[A/G]GAGGGAGCCCCGAGC	90678
rs747659617	snp	A/G	0.000197258	0.00992926	splice-acceptor-variant	LRSAM1	GRCh38.p7	9:127489443	GTGGTCTGTGTTGCA[A/G]AGCGCGATGCAGAAG	90678
rs747665047	in-del	-/G			intron-variant	LRSAM1	GRCh38.p7	9:127500155	CACCTGAAGTCAAAA[-/G]CTTGAGACCAGCCTG	90678
rs747681215	snp	A/G	0.000103357	0.00718805	intron-variant	LRSAM1	GRCh38.p7	9:127479809	TCTGAGGGGGTCCCA[A/G]GGGCTCAGGACCCCT	90678
rs747728956	snp	A/G	0.000160154	0.00894713	intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127450706	ACAAATGTGAAAAAA[A/G]TGCCCCTTGGAGGGG	90678
rs747767926	snp	G/T			intron-variant	LRSAM1	GRCh38.p7	9:127477680	ACTAGAGCCCAGGAG[G/T]TCGCGGCTGCAGTGA	90678
rs747795244	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127474879	GCCGCCATCCCCAAG[C/G]CTCATGATCCAGGGT	90678
rs747832074	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127494331	CATGTCATGCCAGCC[C/T]TCACTGAACAGCTCC	90678
rs747839221	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127493461	GCTGCATACCCTTTT[C/T]GAGCAGCCTGTTTCC	90678
rs747861339	snp	G/T			intron-variant	LRSAM1	GRCh38.p7	9:127459523	CACGCCTGACCAATT[G/T]TACCACTTTGAGCCA	90678
rs747872731	snp	A/C	8.23676e-05	0.00641693	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127473879	TCGAGAACTCTCGGG[A/C]CAGCCCTGATGGGCC	90678
rs747891207	snp	C/G	1.64814e-05	0.00287061	intron-variant	LRSAM1	GRCh38.p7	9:127473772	GCTGTCTCCTCCCTC[C/G]TGGTCAGCTTGTGTC	90678
rs747910258	snp	A/C	3.43501e-05	0.00414414	intron-variant	LRSAM1	GRCh38.p7	9:127496119	CAGCCGTCTGCATGG[A/C]GGGGAGGGGCACGCA	90678
rs748095281	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127488402	AAGTAGCTAGGATTA[C/T]GGGCACCCACCAACA	90678
rs748096307	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127498104	AGGCTCTGGACAGGG[C/T]ATTTTTAGCCAGAGC	90678
rs748122042	snp	A/T	1.64765e-05	0.00287019	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127461242	CTGACCCAGCTCCAG[A/T]CTCTCAATGTTAAAG	90678
rs748134215	in-del	-/TTCTT			intron-variant	LRSAM1	GRCh38.p7	9:127493482	GCCTGTTTCCGCACA[-/TTCTT]TTCAAGTCATTAAAC	90678
rs748144981	snp	C/G	1.66424e-05	0.0028846	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127481197	GACAAAAGAAAAGCT[C/G]CGAGATTTTGAAATC	90678
rs748153917	snp	C/G	1.71381e-05	0.00292724	intron-variant, utr-variant-5-prime	LRSAM1	GRCh38.p7	9:127454482	CAGTCCCTAACTTCT[C/G]TCCTGTGCCCCAGGG	90678
rs748161826	snp	C/T	1.68801e-05	0.00290512	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127492835	CGCTGGGCCCTCAGC[C/T]CCCTGCTCCAGCAGC	90678
rs748172463	snp	A/G	0.000155509	0.00881648	utr-variant-5-prime, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451349	GTCGGATGAACCCGG[A/G]TTCGGGACGACCGAA	90678
rs748178722	snp	C/T			intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127450843	TCTGTGCAGAGGGAG[C/T]CCCGAGCCACAGCCC	90678
rs748185533	snp	C/T	3.31824e-05	0.00407309	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127501106	CTGCAGAGCTGGAGG[C/T]GCAGGCCTCAGAGTG	90678
rs748220042	snp	A/G			intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127449845	AATCAGAGCACAGCT[A/G]TCACCATAGCATAAA	90678
rs748259640	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127498037	TGGGGAAGAGGTGAG[A/G]GGCCAGAGCAGGGGT	90678
rs748321543	snp	A/T			intron-variant	LRSAM1	GRCh38.p7	9:127481462	ACCGTGTTAACCAGG[A/T]TGGTTTCGATCTCCT	90678
rs748337361	in-del	-/G	1.79514e-05	0.00299589	intron-variant	LRSAM1	GRCh38.p7	9:127481276	TTTTTTTTTTGAGAC[-/G]GGAGTCCTGCACTGT	90678
rs748349115	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127497066	TGAGGCCTGGGGAGG[C/T]TGCCCTCACAGCTAT	90678
rs748358043	snp	A/G	1.65282e-05	0.00287469	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127501033	CCACCAATGGGTGAG[A/G]TCGTCACCCCTACGG	90678
rs748384913	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127484689	TCCATTCATCTATCA[A/G]TGGGAATGTGGGTTG	90678
rs748430522	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127492738	GCCCTTCTCCATCCT[C/G]CCACTGCGGGACTCC	90678
rs748439646	snp	A/G	1.64909e-05	0.00287144	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127479388	TGTCTTGCAGGAACA[A/G]AAGATGCTGGAGAAA	90678
rs748478852	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127478587	AACCGGGTGCTGTAG[A/G]TGTGTTACGCAGACA	90678
rs748529476	snp	C/T	4.55581e-05	0.00477252	intron-variant, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127487631	CACATAGTAGGTGCT[C/T]GGGAAACGTTCCAAG	90678
rs748536393	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127477327	GTTATCTGTATAATT[A/G]AAGATTAATTTTAAA	90678
rs748573602	snp	G/T			intron-variant	LRSAM1	GRCh38.p7	9:127490777	TACTACTACCACTGT[G/T]ACTCAGTCACTTCCA	90678
rs748590846	in-del	-/T			intron-variant	LRSAM1	GRCh38.p7	9:127470089	TTACCTTAAAAATTA[-/T]TCTCAATATCTACTC	90678
rs748618591	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127455733	CTCCTTTCTCTCTGC[C/T]TCTTATGCTCTTGGC	90678
rs748661381	snp	A/G			downstream-variant-500B	LRSAM1	GRCh38.p7	9:127503990	TTTCCGGCAGACGGC[A/G]TTGAGCCAGGTGCAG	90678
rs748736522	snp	A/C	1.65031e-05	0.00287251	synonymous-codon, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127449634	TCTGTTCTGAATGGT[A/C]AGTTTCACTGTAATC	90678
rs748752390	snp	A/T	1.64727e-05	0.00286986	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127455022	GCTGGGGCAGATGAC[A/T]TTCTCGACATCTCTA	90678
rs748775036	snp	C/T	1.65466e-05	0.00287628	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127457330	GGTGCTGATCGTCCA[C/T]ACGAATCACCTCACT	90678
rs748778245	snp	C/T	4.94882e-05	0.0049741	intron-variant	LRSAM1	GRCh38.p7	9:127455658	GAGACTTTCTTGTTG[C/T]ATGTCTGCTTGTTTG	90678
rs748826298	snp	A/G	1.90878e-05	0.00308926	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127487759	TCAGCCAGATCCTGC[A/G]GGAGGTGAGCCCTCG	90678
rs748852615	snp	C/T	3.29647e-05	0.00405971	intron-variant	LRSAM1	GRCh38.p7	9:127473768	CTCAGCTGTCTCCTC[C/T]CTCCTGGTCAGCTTG	90678
rs748853481	snp	A/G	1.70142e-05	0.00291664	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127496017	GGAGCTGTCGGCTGA[A/G]CACTACCTGCCCATC	90678
rs748939177	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127472932	CCCCTAGGGTGTGTG[A/G]GAGGGCACGAGCGCC	90678
rs748949441	snp	G/T			intron-variant	LRSAM1	GRCh38.p7	9:127457810	AGCCCAGGGTTGTTA[G/T]GCGCAGACCTGAGCT	90678
rs748957383	snp	G/T			intron-variant	LRSAM1	GRCh38.p7	9:127499761	TGGTGAAACCCTGTC[G/T]CTACTAAAATTAGCT	90678
rs749012928	in-del	-/T	1.66051e-05	0.00288137	frameshift-variant, intron-variant, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127495414	CCTTGTCCTTGAAGC[-/T]GCAAGTAAGGACTGC	90678
rs749082485	snp	A/T			intron-variant	LRSAM1	GRCh38.p7	9:127481813	GTAATCCCAGCACTT[A/T]GGGAGGCCGAGGTGG	90678
rs749085527	snp	A/C			intron-variant	LRSAM1	GRCh38.p7	9:127486269	TCTTGACTGTGGTAC[A/C]CTCATCAGTGTCTGA	90678
rs749100440	snp	A/C	3.30502e-05	0.00406497	intron-variant	LRSAM1	GRCh38.p7	9:127480000	CTCTGCTCCTCGGCC[A/C]CAGCCCCAGAGTCCT	90678
rs749192098	snp	C/T	6.67601e-05	0.00577716	missense, intron-variant, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127491290	CTGGACACAGAGTCA[C/T]TCCAGGTATGTAGGG	90678
rs749204843	snp	C/G/T	4.96457e-05	0.00498205	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127501090	AGGCCATCCGCTCCC[C/G/T]CTGCAGAGCTGGAGG	90678
rs749230931	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127497873	TGTGCATGAACCACG[C/T]TGAGGAACCTCCGGA	90678
rs749239725	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127485417	AAAAAATTAGGCGGG[C/T]GTGGTGGCAGGCGTC	90678
rs749249459	snp	C/T			intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127449520	TCACTCTCGGCTCAC[C/T]ACTGGTGGCAGAAAT	90678
rs749299326	snp	A/G	3.30677e-05	0.00406605	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127501024	GAGCTGAAACCACCA[A/G]TGGGTGAGGTCGTCA	90678
rs749299792	snp	C/T	3.30169e-05	0.00406293	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127459035	TAATCAGCTGACAGC[C/T]CTTCCTGACGATCTG	90678
rs749307938	snp	A/T	1.64923e-05	0.00287156	intron-variant	LRSAM1	GRCh38.p7	9:127479368	CTGACAGTCACCAGG[A/T]TCTGTGTCTTGCAGG	90678
rs749320612	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127496940	AAGTGGCTGAGGTGT[A/G]CAGGTGAAGCCTGGC	90678
rs749357519	snp	C/G	1.71687e-05	0.00292986	intron-variant	LRSAM1	GRCh38.p7	9:127485876	GTGAGGGAGCTGGGG[C/G]AGCTGGCTCAGGGCC	90678
rs749401286	snp	A/G	4.99629e-05	0.0049979	intron-variant	LRSAM1	GRCh38.p7	9:127473980	TGTGTGTGTGCGTGT[A/G]CATGTATGTGTGTTG	90678
rs749407044	snp	A/C	3.3942e-05	0.00411945	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127496029	TGAGCACTACCTGCC[A/C]ATCTTTGCGCACCAC	90678
rs749417504	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127469826	AAAAATTAGCAAGGC[A/G]TGGTGGCGGGCGCCT	90678
rs749454115	in-del	-/TT			intron-variant	LRSAM1	GRCh38.p7	9:127484803	TTTTTTGATTTTTCT[-/TT]TTTTTTCTTTTTTTT	90678
rs749497603	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127477030	GAACTCTATGCATAT[A/G]TAAAGATTCATAGAA	90678
rs749575647	snp	C/T	1.64904e-05	0.00287139	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127485774	GAGAGCTGTAAGAAC[C/T]GGCTCATCCAGATGG	90678
rs749592869	snp	C/T	3.29495e-05	0.00405877	intron-variant	LRSAM1	GRCh38.p7	9:127455096	GAATTGGATCTGTCC[C/T]GTTTTCTTGGATCTT	90678
rs749609283	snp	A/T	1.64727e-05	0.00286986	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127455006	TCCTTAGGCAAAAGA[A/T]GCTGGGGCAGATGAC	90678
rs749626964	in-del	-/TTG			upstream-variant-2KB, intron-variant, utr-variant-5-prime	RPL12, LRSAM1	GRCh38.p7	9:127451785	TGCTCCCTCGAGCAC[-/TTG]TTGTGTGCACTTTAG	90678
rs749630146	snp	G/T	3.3644e-05	0.00410132	intron-variant	LRSAM1	GRCh38.p7	9:127495298	ATTTTGTGACTAACA[G/T]TGCCTGCTTCATTCC	90678
rs749635888	snp	A/G	1.64741e-05	0.00286998	intron-variant	LRSAM1	GRCh38.p7	9:127462378	GAACCCTGGAGGTAA[A/G]TGGGAAGCTGTTCTT	90678
rs749662590	snp	A/G	1.69146e-05	0.0029081	intron-variant	LRSAM1	GRCh38.p7	9:127495438	GGACTGCTGGTGCCT[A/G]TCCCGGCCAGGGAGC	90678
rs749673102	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127489759	TCTTGCCAGCGAGGC[A/G]GGTCTCCACCACGCC	90678
rs749688098	snp	A/C	1.68386e-05	0.00290155	utr-variant-3-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127502926	CCACCTGGGCCTGGT[A/C]CTAGCCCTGCCTCGG	90678
rs749714585	snp	A/C			intron-variant, utr-variant-5-prime	LRSAM1	GRCh38.p7	9:127454414	CAGACCAGCTGCATG[A/C]TCTGTGTTACTGCAC	90678
rs749729648	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127501981	CAGACAGCTTTGAGC[A/G]GAGCTTGGATCAGTT	90678
rs749802520	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127469528	TATCTGAAAAAATTG[C/G]ACAACATCATCTTAG	90678
rs749845188	snp	C/T	0.0016116	0.0283409	intron-variant	LRSAM1	GRCh38.p7	9:127481256	CAGGGGAGGGCAGCA[C/T]TTTTTTTTTTTTTTT	90678
rs749850642	snp	C/T	3.29582e-05	0.00405931	stop-gained, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127462293	ACCGTGGGGGAGCTT[C/T]GAAGCCTGCGTACCC	90678
rs749885530	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127473214	GATAACTTTGAGTAC[A/G]TCAAAACTTACAACT	90678
rs749937142	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127487840	GAGTGCAGAGCTCCA[C/T]ACGGAGCCCTTCCTA	90678
rs750027134	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127498764	TATACTTTATATCAA[A/G]TATAGAGGCTGGGGC	90678
rs750060771	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127486183	TCTGAGAAACTGTAT[A/G]ACGCACCCAAGGAAG	90678
rs750151479	snp	A/C	1.65015e-05	0.00287237	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127479426	TTGAACGGCGCCTGG[A/C]ACTGGGGCAGCGGGA	90678
rs750152286	snp	A/G	1.72293e-05	0.00293503	intron-variant	LRSAM1	GRCh38.p7	9:127501152	ACGGGAGGTAAGTCC[A/G]GGGCCCTCCCCACCC	90678
rs750177689	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127469232	CCCAGCACTTTGGGA[C/G]GCTGAGGTGGGCAGA	90678
rs750206018	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127465462	TATAGCCCACAGTCC[A/G]TGCCCTTAAGCCACC	90678
rs750222188	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127496186	CCTTGTGTAGTCCTC[A/G]TTGAGGCCTGTCCTT	90678
rs750243357	snp	A/G	1.79412e-05	0.00299505	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127487686	GGCAGCATGGCCGAA[A/G]TGGATGAACGATTCC	90678
rs750249034	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127463982	AGAGATCGTTGTAAA[C/T]CAGGCCGTCTGAAGC	90678
rs750279254	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127471648	AAAGACTAGCCAGGC[A/G]TGGTGATGCATGCCT	90678
rs750319510	in-del	-/AC	1.66441e-05	0.00288474	frameshift-variant, intron-variant, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127491279	AGAGGAAGTCCCTGG[-/AC]ACAGAGTCACTCCAG	90678
rs750337168	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127478253	CCACCCTGCACTCCC[A/G]TTGCCTGGAGGTAGT	90678
rs750402799	snp	A/G	1.65696e-05	0.00287828	splice-donor-variant, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127485836	GCAGGCCTGTTCCAG[A/G]TAAGGTAAGGAAGAG	90678
rs750477515	snp	C/T	1.6557e-05	0.00287719	synonymous-codon, intron-variant, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127495400	TTTGAACCAGAAGCC[C/T]TTGTCCTTGAAGCTG	90678
rs750505340	snp	C/G	1.73453e-05	0.00294489	intron-variant	LRSAM1	GRCh38.p7	9:127495953	TCATGGTACACGTTT[C/G]TGTCTTGCAGGAAGA	90678
rs750514562	snp	C/T			missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127461216	TGCAGCTCCCACGTT[C/T]CATTGGGAACCTGAC	90678
rs750570495	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127455241	GCCTCAATATAACGT[A/G]GTCTCCAAGAGTCAA	90678
rs750618461	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127494123	GTAGGCCTTGGGGGT[C/T]ACCACCAAAGGAGGA	90678
rs750643007	snp	C/G			downstream-variant-500B	LRSAM1	GRCh38.p7	9:127503778	CCCTGTGTGTTCCGT[C/G]CATTATCCCAGTGAG	90678
rs750749720	snp	A/G	1.73963e-05	0.00294921	intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451238	CGCGGCAGGGCCGAG[A/G]GATGCTCCATCCCGC	90678
rs750765132	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127469241	TTGGGAGGCTGAGGT[A/G]GGCAGATAACCTGAG	90678
rs750784469	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127502560	GGTATGGTGGTGCAC[A/G]CCTGTAGTCCCAGCT	90678
rs750833777	snp	A/G	2.43775e-05	0.00349115	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127489473	GGCTGCGTTCGAGGC[A/G]CTCCAGGTGAAGAAA	90678
rs750921683	snp	A/C	1.65056e-05	0.00287272	intron-variant	LRSAM1	GRCh38.p7	9:127458990	GAGACTCACAGGGGT[A/C]TTTCTTCTGCAGGTT	90678
rs750926002	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127495253	CCACCGCGCCTGGCA[A/G]CCATCATTGTTATTA	90678
rs750936430	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127461899	GAGAACAACAGTGGC[A/G]CCCCATTGCTCAGCC	90678
rs750961361	snp	G/T	1.74075e-05	0.00295016	intron-variant	LRSAM1	GRCh38.p7	9:127457423	TCCCAGGCAGCTGGG[G/T]CTCTGCATGGGGTTC	90678
rs750981844	snp	A/G	1.66441e-05	0.00288474	splice-donor-variant	LRSAM1	GRCh38.p7	9:127497335	CCAGGATCCAGCCAG[A/G]TACAAGCACAGCTCC	90678
rs750994961	snp	A/G	0.00024776	0.0111274	intron-variant	LRSAM1	GRCh38.p7	9:127473934	GTTAGAGTGGCAGGT[A/G]AGACAAGGCAGCCTG	90678
rs750997053	in-del	-/TCT	1.67276e-05	0.00289197	cds-indel, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127454535	AGGGAAGGATGCCGC[-/TCT]TCTTCCGGAAGCGGA	90678
rs751032066	snp	G/T			intron-variant	LRSAM1	GRCh38.p7	9:127486103	AAGCGATGAACCACA[G/T]TCGCTGATTGATTCT	90678
rs751051547	in-del	-/TTT			intron-variant	LRSAM1	GRCh38.p7	9:127481256	CAGGGGAGGGCAGCA[-/TTT]TTTTTTTTTTTTTGA	90678
rs751061978	snp	A/G	3.44015e-05	0.00414724	utr-variant-5-prime, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451331	ATGGTGGAGGCGGCT[A/G]GTGTCGGATGAACCC	90678
rs751110136	snp	A/G	3.31494e-05	0.00407107	intron-variant	LRSAM1	GRCh38.p7	9:127491202	AAAAAACCCTGTCTC[A/G]TCTTCTGTTTAGATT	90678
rs751112533	in-del	-/AAA	1.67027e-05	0.00288982	intron-variant	LRSAM1	GRCh38.p7	9:127491184	GTGGTTAATGTGAGT[-/AAA]AAAAAACCCTGTCTC	90678
rs751228318	snp	C/T	1.7809e-05	0.00298398	intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127449568	GAGGGTTGCTACCTG[C/T]CCCCCCACCCTCCTC	90678
rs751273880	snp	A/G	1.65619e-05	0.00287762	intron-variant	LRSAM1	GRCh38.p7	9:127500991	ACCCTGGCTCAGTCT[A/G]TCTGTCTGGTCCCCA	90678
rs751296192	snp	C/T	1.64985e-05	0.0028721	intron-variant	LRSAM1	GRCh38.p7	9:127479338	TTCTGTGTCCTAACT[C/T]CCCCAGGGCCTGTGC	90678
rs751314768	snp	G/T	3.30104e-05	0.00406252	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127485815	TCAGAGGCAGAACTT[G/T]GTCCAGCAGGCCTGT	90678
rs751408018	in-del	-/T			intron-variant	LRSAM1	GRCh38.p7	9:127465068	ACTGTGGGCAAGATC[-/T]TCAGGTGTCACGCAC	90678
rs751418671	in-del	-/TGT			intron-variant	LRSAM1	GRCh38.p7	9:127468522	GCAACCAAGACACAC[-/TGT]ATGCCTATGACTTAT	90678
rs751429630	snp	A/G	1.6473e-05	0.00286988	intron-variant	LRSAM1	GRCh38.p7	9:127455068	AGGTAAACTGAGGAT[A/G]GTGTTGGGCTGTGAA	90678
rs751523580	snp	G/T			utr-variant-3-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127503496	TAAACCTGTCTTCAG[G/T]GCGCTTCTGGCCTGA	90678
rs751553514	snp	G/T			intron-variant	LRSAM1	GRCh38.p7	9:127467311	ACTATCACAAAGGGA[G/T]AAATGCAGGGGCTTT	90678
rs751593173	snp	C/T	8.19907e-05	0.00640224	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127489448	CTGTGTTGCAGAGCG[C/T]GATGCAGAAGGCTGC	90678
rs751635583	snp	A/G	7.60109e-05	0.00616439	utr-variant-3-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127502900	TACCACAGCAGCTGA[A/G]TGCTGCCCGCCCACC	90678
rs751712659	snp	C/T	1.66563e-05	0.0028858	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127479880	GAGTGAGCACCAGCG[C/T]CACCTCAACGCAGAG	90678
rs751727967	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127469086	TTGCAATACATATAT[A/G]TCCAACAAAGGACTG	90678
rs751768471	snp	A/G	1.74211e-05	0.00295132	intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451232	TGCACGCGCGGCAGG[A/G]CCGAGGGATGCTCCA	90678
rs751817914	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127482559	GGAAAGTGCCCATTT[C/G]TCCACCACCATCACC	90678
rs751826919	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127480845	GGCTTGGGCCACCAC[A/G]CCTGGCTAATTTTTG	90678
rs751859968	snp	A/G	1.66078e-05	0.00288161	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127497312	AGTCCAGGAACTGCT[A/G]GATGCAGCCAGGATC	90678
rs751872462	snp	A/G	1.69421e-05	0.00291046	intron-variant	LRSAM1	GRCh38.p7	9:127457401	CCATCAAGGTACTGG[A/G]CCCTCCTCCCAGGCA	90678
rs751875555	snp	A/C/G	4.95273e-05	0.00497611	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127489468	CAGAAGGCTGCGTTC[A/C/G]AGGCACTCCAGGTGA	90678
rs751928830	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127495140	ATTTTTAGTAGAGGT[A/G]GGGGGTTTCTCCATG	90678
rs751939984	in-del	-/TA			intron-variant	LRSAM1	GRCh38.p7	9:127472300	AACTATGTAGAAGTA[-/TA]TATATATATATATGT	90678
rs751958829	snp	C/T	1.67033e-05	0.00288987	intron-variant	LRSAM1	GRCh38.p7	9:127497213	CCATTTAGCGGGCTC[C/T]CGCCCAGGCCACAGT	90678
rs751963482	snp	C/T	0.000103148	0.00718075	intron-variant	LRSAM1	GRCh38.p7	9:127489409	GGAAAAGTGTGGGCA[C/T]GGCCCCTGCTGAGGG	90678
rs751974896	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127460412	AGCCCTGGTTCAGTC[C/T]CAGCACCACTGCCGG	90678
rs752012848	snp	G/T	0.00102222	0.0225847	intron-variant	LRSAM1	GRCh38.p7	9:127455654	TTCAGAGACTTTCTT[G/T]TTGCATGTCTGCTTG	90678
rs752014899	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127494203	AGAGGGGCTGCAGCC[C/T]GGGAGGGCCAACGAC	90678
rs752028583	snp	A/G	0.00013332	0.00816347	intron-variant	LRSAM1	GRCh38.p7	9:127457298	CAGCCCAGCATGGCC[A/G]CACATCTCTCCACAC	90678
rs752069308	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127501676	GGCAGAGATTGCAGT[A/G]AGCCAAGATCCCACC	90678
rs752128674	snp	C/T	1.64882e-05	0.00287121	intron-variant	LRSAM1	GRCh38.p7	9:127473753	GGTGTCTCTGGGTAC[C/T]TCAGCTGTCTCCTCC	90678
rs752175786	in-del	-/GCATGTCTGC	0.000131876	0.00811915	intron-variant	LRSAM1	GRCh38.p7	9:127455657	AGAGACTTTCTTGTT[-/GCATGTCTGC]TTGTTTGAACCCACA	90678
rs752177472	snp	A/C	4.79168e-05	0.0048945	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127483005	ACTGAGAGCCTGCGG[A/C]GACGTGACGTTGCCT	90678
rs752186146	snp	C/T	1.65954e-05	0.00288053	intron-variant	LRSAM1	GRCh38.p7	9:127500965	CCCAGGGGTTAGGGT[C/T]AGCGGAGATGACCCT	90678
rs752192417	snp	C/G	1.64781e-05	0.00287033	intron-variant	LRSAM1	GRCh38.p7	9:127478988	TGCCTTTACCCTTCT[C/G]TCACTCTTTTCTCAT	90678
rs752197302	snp	A/T			intron-variant	LRSAM1	GRCh38.p7	9:127495558	TGTGCCAAGCCCCAG[A/T]GGAGACAGAAGCGAG	90678
rs752208982	snp	C/T	1.65045e-05	0.00287263	intron-variant	LRSAM1	GRCh38.p7	9:127458995	TCACAGGGGTCTTTC[C/T]TCTGCAGGTTCTAGA	90678
rs752370625	snp	A/T	1.64963e-05	0.00287192	intron-variant	LRSAM1	GRCh38.p7	9:127473948	TAAGACAAGGCAGCC[A/T]GCTGCACGCATACAT	90678
rs752408952	in-del	-/A	1.72904e-05	0.00294022	intron-variant	LRSAM1	GRCh38.p7	9:127479796	CCCCTCACGGCGTCT[-/A]GAGGGGGTCCCAGGG	90678
rs752464988	snp	A/C	1.81524e-05	0.00301262	intron-variant	LRSAM1	GRCh38.p7	9:127492934	TCAGCATCACACAGG[A/C]ATTTGCTTTTCTTTA	90678
rs752477588	snp	A/G	1.6513e-05	0.00287336	synonymous-codon, intron-variant, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127495349	CAAAAGTGAAACCAG[A/G]CAGGAAAATTACTGG	90678
rs752478850	snp	A/G	3.03864e-05	0.00389772	intron-variant	LRSAM1	GRCh38.p7	9:127483038	GAGTTTTGGGATGGG[A/G]AGCTTGTGAGCACGC	90678
rs752519180	snp	A/C	3.01746e-05	0.00388412	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127502881	CGCCCAGCGCCTCCG[A/C]ATCTACCACAGCAGC	90678
rs752591010	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127489340	CTCAGAAAAAACCCA[C/T]CCATTAAGGTGCTTT	90678
rs752596738	snp	C/G/T	8.34531e-05	0.00645917	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127454549	CTCTTCTTCCGGAAG[C/G/T]GGAAACCCAGTGAGG	90678
rs752637543	snp	C/G			upstream-variant-2KB, intron-variant	RPL12, LRSAM1	GRCh38.p7	9:127452362	CATTCCCCATCCTTG[C/G]AGGCAGGTGGGGTGA	90678
rs752646771	snp	A/C	1.66946e-05	0.00288912	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127479866	CTGGAGCAGGGCCTG[A/C]GTGAGCACCAGCGCC	90678
rs752678501	snp	A/G	1.94037e-05	0.00311472	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127502821	CTGCTGCTGCCAGCA[A/G]TGCTGCCAGCCACTG	90678
rs752751533	snp	A/G	1.64953e-05	0.00287182	intron-variant	LRSAM1	GRCh38.p7	9:127462221	TGATGGGGATTTGGG[A/G]TGTTGAGCTGTGCTA	90678
rs752753388	snp	A/C	5.13483e-05	0.00506671	intron-variant	LRSAM1	GRCh38.p7	9:127479546	AGCCTGGCTGCATCC[A/C]CCAGCCAGTGGCCTC	90678
rs752782181	snp	C/G	5.66396e-05	0.00532133	missense, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127450799	CTCCGGTGCACCTCA[C/G]GTATACTGGGGGAAA	90678
rs752814857	snp	C/T	1.81879e-05	0.00301557	intron-variant	LRSAM1	GRCh38.p7	9:127501167	GGGGCCCTCCCCACC[C/T]GCCTGCCCTGCCTGT	90678
rs752817719	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127465878	GGATGGGGCAGTTCT[A/G]TGGCTGTGAGCTGAG	90678
rs752836939	snp	A/C	1.67761e-05	0.00289617	intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127449722	GACTAGAAATAAAGG[A/C]ATGTAATCAACATGG	90678
rs752844497	snp	A/G	2.38126e-05	0.00345047	intron-variant	LRSAM1	GRCh38.p7	9:127487814	AGGAGGGAGGTTCAG[A/G]AGCCAGGGCAGAGTG	90678
rs752866150	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127480743	CTGAGGCTGGAGTGC[A/G]GTGGTGTGCTCTCGG	90678
rs752875375	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127473987	GTGCGTGTGCATGTA[C/T]GTGTGTTGAGGGAGC	90678
rs752926906	snp	C/T	1.66935e-05	0.00288903	intron-variant	LRSAM1	GRCh38.p7	9:127457291	TCTTCCTCAGCCCAG[C/T]ATGGCCGCACATCTC	90678
rs752939083	snp	G/T			intron-variant	LRSAM1	GRCh38.p7	9:127493034	TACAAAGGAAAATAA[G/T]TGCATTTCCAAGCGT	90678
rs752953975	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127494030	TACTGCCATCTCCTA[C/T]GCATCAGGTTACTTT	90678
rs753004252	snp	C/G	1.77839e-05	0.00298189	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127487722	ATTCTGTCGTGGCAG[C/G]AAATGGATCAGAACA	90678
rs753006222	snp	C/T	3.47977e-05	0.00417105	intron-variant	LRSAM1	GRCh38.p7	9:127496142	GGCACGCAAGGCCGC[C/T]GTCCTGACCAGCCGG	90678
rs753041879	snp	A/C			intron-variant	LRSAM1	GRCh38.p7	9:127455423	CAACACCACTGCTTG[A/C]CAGCCTTGCCCCTGG	90678
rs753065796	snp	A/C			intron-variant	LRSAM1	GRCh38.p7	9:127458013	AGTTTGGTTGAATCC[A/C]TAGATATGGAGGGTA	90678
rs753072076	snp	A/C			intron-variant	LRSAM1	GRCh38.p7	9:127473122	TTCCTTGATTCTGTG[A/C]ATATTTTTCATACGT	90678
rs753087190	snp	C/T	1.66821e-05	0.00288804	intron-variant	LRSAM1	GRCh38.p7	9:127481236	ATGAAAGGTAAGTGT[C/T]CTTCCAGGGGAGGGC	90678
rs753098074	snp	A/G	1.68499e-05	0.00290253	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127496053	GCACCACCGCCTCTC[A/G]CTGGACCTGCTGAGC	90678
rs753149497	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127496958	GGTGAAGCCTGGCAC[C/T]GGGAAGCAGTTGCTA	90678
rs753217318	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127494256	CAGGTCCAGGAGGGG[C/T]CCGCAAAGGGCAGTC	90678
rs753246657	snp	C/T	1.66418e-05	0.00288455	intron-variant	LRSAM1	GRCh38.p7	9:127481137	CAGTGAGACAGGAAA[C/T]AGGCCTGCTGGTGAC	90678
rs753276297	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127488235	TGACCTCCTCCCCTT[C/T]GGTGTCCATATTACT	90678
rs753337691	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127461372	GGGCAGCCAGTCTCC[A/G]GGGGTCGCTGTAAAT	90678
rs753354068	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127474852	TGCCACATTAGCCTG[C/T]GTGCCCCCTCTGCCG	90678
rs753418696	snp	C/G	0.000131952	0.0081215	intron-variant	LRSAM1	GRCh38.p7	9:127483025	TGACGTTGCCTGTGA[C/G]TTTTGGGATGGGGAG	90678
rs753421683	snp	G/T	3.63676e-05	0.00426409	intron-variant	LRSAM1	GRCh38.p7	9:127454620	GGAAAGTGGGTTTCC[G/T]CTAACTCTATCCCAT	90678
rs753445924	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127489171	CTGAGTGTCACTCCC[C/T]ATCTGTGAAGTGGGG	90678
rs753496932	in-del	-/AA			intron-variant	LRSAM1	GRCh38.p7	9:127456164	AAATGAGAATATGCA[-/AA]AAAAAAAAAAAAAAA	90678
rs753536686	snp	A/C	1.67139e-05	0.00289079	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127454539	AAGGATGCCGCTCTT[A/C]TTCCGGAAGCGGAAA	90678
rs753575542	snp	C/T	0.00175146	0.0295408	intron-variant	LRSAM1	GRCh38.p7	9:127501159	GTAAGTCCGGGGCCC[C/T]CCCCACCCGCCTGCC	90678
rs753583238	snp	A/G	1.65031e-05	0.00287251	intron-variant	LRSAM1	GRCh38.p7	9:127462211	AGGAAGCTGGTGATG[A/G]GGATTTGGGGTGTTG	90678
rs753583894	snp	A/G/T	7.18434e-05	0.0059931	intron-variant	LRSAM1	GRCh38.p7	9:127481277	TTTTTTTTTTGAGAC[A/G/T]GAGTCCTGCACTGTC	90678
rs753620889	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127473637	CTGCCACATTCCAGG[C/G]CCAGGGCTAGGACCG	90678
rs753648728	snp	C/T			upstream-variant-2KB, intron-variant	RPL12, LRSAM1	GRCh38.p7	9:127452098	AGGTCAGCCACTGCC[C/T]ACCCCACCCCAGGAA	90678
rs753650841	snp	C/T	1.83421e-05	0.00302832	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127502803	CCTCAACTGTGGCCA[C/T]GTCTGCTGCTGCCAG	90678
rs753670711	snp	A/C/G	5.08335e-05	0.00504129	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127492821	TGATCTCGGAGCAGC[A/C/G]CTGGGCCCTCAGCTC	90678
rs753782196	snp	C/T	0.000103081	0.00717843	intron-variant	LRSAM1	GRCh38.p7	9:127487784	CCCTCGCCCAGAGCC[C/T]GAGGGTGGGAGCTCA	90678
rs753819821	snp	A/T			intron-variant	LRSAM1	GRCh38.p7	9:127486011	TAGCCGGATCCATGA[A/T]TCAGTGTTGGGCTGT	90678
rs753843052	snp	A/G	1.66178e-05	0.00288247	missense, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127449705	CACCAACTTTTTTTG[A/G]AGACTAGAAATAAAG	90678
rs753897147	snp	A/G	1.76269e-05	0.00296869	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127487702	TGGATGAACGATTCC[A/G]GCAGATTCTGTCGTG	90678
rs753956691	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127478488	TAGATGTATGAGTTA[C/T]TTCCAGTGTTTTTGC	90678
rs753979299	snp	A/C/T	3.3719e-05	0.00410592	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127496047	CTTTGCGCACCACCG[A/C/T]CTCTCACTGGACCTG	90678
rs754046743	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127491965	GGTGTGTGAGGACAT[A/G]TGCCTGTGCCAGGAG	90678
rs754062373	snp	A/G	2.3799e-05	0.00344949	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127467787	CCCGCCGCGGGAGGT[A/G]TGTGGTGCCGGCACT	90678
rs754080605	snp	A/C	1.65641e-05	0.00287781	intron-variant	LRSAM1	GRCh38.p7	9:127480028	CCTTCCCCGTGCAGT[A/C]CCCTGAGGAGCCGGG	90678
rs754095363	snp	A/G	1.64757e-05	0.00287012	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127455604	CTTTTGCAACATGCA[A/G]AGTTCTGCAGAAGAA	90678
rs754120092	snp	A/C			intron-variant	LRSAM1	GRCh38.p7	9:127457280	CTGCCTGCTGCTCTT[A/C]CTCAGCCCAGCATGG	90678
rs754134527	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127471883	GACCAGGGTGGTCTC[A/G]TACTCTTGACCTAAG	90678
rs754162095	snp	C/T	0.000186595	0.00965725	intron-variant	LRSAM1	GRCh38.p7	9:127467734	GGGTTACCCTTGTGT[C/T]TGCAGATGCTGAGCC	90678
rs754165447	in-del	-/CTGT	1.64743e-05	0.00287	intron-variant	LRSAM1	GRCh38.p7	9:127478914	ACCCTCTCTTGACCA[-/CTGT]CTTTTTTTCCTCCCA	90678
rs754216773	in-del	-/A	3.295e-05	0.00405881	intron-variant	LRSAM1	GRCh38.p7	9:127455528	CTCAGAGAACAAGCT[-/A]AAAACTGGCAGGAGG	90678
rs754248018	snp	A/G	8.2558e-05	0.00642434	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127479977	CTGCAGGACAATCAG[A/G]GGTTGGGCTCTGCTC	90678
rs754251340	snp	C/G			intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451025	CCCAGGCCAATGGGG[C/G]GAAACGCCCGGAGAC	90678
rs754297824	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127470283	GCCTCAGGAAACTTA[C/G]AGTCATGGTGGAAGG	90678
rs754309449	snp	C/G	1.71743e-05	0.00293033	intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451258	CTCCATCCCGCAGCC[C/G]CGGCCACAACCAGAG	90678
rs754358178	snp	A/C			intron-variant	LRSAM1	GRCh38.p7	9:127484088	AACTCCCCGTGCCCC[A/C]CTCCCCTCAGCCCCT	90678
rs754374008	snp	A/C	3.29457e-05	0.00405854	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127455000	TTTTTATCCTTAGGC[A/C]AAAGAAGCTGGGGCA	90678
rs754459198	snp	A/C/T	4.98387e-05	0.00499172	intron-variant	LRSAM1	GRCh38.p7	9:127459100	AACAGAAACCCACCT[A/C/T]GGATGGCCTTAGTGA	90678
rs754499152	snp	A/G	1.75616e-05	0.00296319	intron-variant	LRSAM1	GRCh38.p7	9:127457430	CAGCTGGGGCTCTGC[A/G]TGGGGTTCCACGCGG	90678
rs754525704	snp	A/G	1.66454e-05	0.00288486	intron-variant	LRSAM1	GRCh38.p7	9:127497231	CCCAGGCCACAGTCT[A/G]CACTTCCTTGAACTG	90678
rs754527468	snp	C/T	3.29478e-05	0.00405867	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127473875	GGAATCGAGAACTCT[C/T]GGGACAGCCCTGATG	90678
rs754527551	snp	A/T			intron-variant	LRSAM1	GRCh38.p7	9:127494310	GCCTGTGTTGATCCC[A/T]CTCCCCATGTCATGC	90678
rs754546639	snp	C/G/T	0.000296647	0.0121755	intron-variant	LRSAM1	GRCh38.p7	9:127473769	TCAGCTGTCTCCTCC[C/G/T]TCCTGGTCAGCTTGT	90678
rs754550052	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127460932	GCAATCTCAGCTCAC[C/T]GCAACCTCTGCCTCC	90678
rs754578966	in-del	-/TTTTTTTT	4.94458e-05	0.00497197	intron-variant	LRSAM1	GRCh38.p7	9:127455651	TCTTCAGAGACTTTC[-/TTTTTTTT]TTGTTGCATGTCTGC	90678
rs754590979	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127459508	ACAGGTGTGAGCCAC[C/T]ACGCCTGACCAATTG	90678
rs754637925	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127474880	CCGCCATCCCCAAGG[C/T]TCATGATCCAGGGTC	90678
rs754642669	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127473385	ACAGCCAAATAGGAA[A/G]TGAGTCTAAGGTATG	90678
rs754732689	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127488259	TATTACTCTGTTTAG[C/T]GTTTTTGTTTTCTTT	90678
rs754785158	snp	A/G	1.65007e-05	0.00287229	intron-variant	LRSAM1	GRCh38.p7	9:127462212	GGAAGCTGGTGATGG[A/G]GATTTGGGGTGTTGA	90678
rs754873042	snp	A/C	1.64746e-05	0.00287002	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127461234	TTGGGAACCTGACCC[A/C]GCTCCAGACTCTCAA	90678
rs754895207	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127486430	TGCCCAGCAGAGCCA[A/G]TGGGGAAAACTCAGT	90678
rs754927709	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127459152	TGGAATGTTCTGGCC[A/G]GGCTCCAGCCAGTGG	90678
rs755004129	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127497947	TGGGGAAACTGAAGC[A/G]CAAAGAGGTTAGCAT	90678
rs755028625	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127463227	AAAAAAAAAATTCTG[A/G]GCAGACCTGGATAAC	90678
rs755056267	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127479685	CTCCCCGTGTGCAGA[C/T]GGACACTGTAGCCTA	90678
rs755058160	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127464403	ACTGGCCACGTGTAT[C/G]TATTGAGCACCTGGA	90678
rs755070977	snp	A/G	7.07539e-05	0.00594743	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127487715	CCAGCAGATTCTGTC[A/G]TGGCAGCAAATGGAT	90678
rs755102176	snp	A/G	1.67458e-05	0.00289355	intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127449720	GAGACTAGAAATAAA[A/G]GCATGTAATCAACAT	90678
rs755106008	snp	C/T			synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127492894	AGAGCTCCGGGAAAT[C/T]CTGGTATGTGTTTGG	90678
rs755107083	snp	A/C	1.64906e-05	0.00287142	intron-variant	LRSAM1	GRCh38.p7	9:127479380	AGGATCTGTGTCTTG[A/C]AGGAACAGAAGATGC	90678
rs755146127	snp	A/C			intron-variant	LRSAM1	GRCh38.p7	9:127478538	GGAAGTTGTACCCAC[A/C]CCTTTGTGCACTGTG	90678
rs755272225	snp	C/T	1.64765e-05	0.00287019	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127455610	CAACATGCAAAGTTC[C/T]GCAGAAGAAGGTAAG	90678
rs755294613	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127491997	TTGAGCAGAGCCTTC[A/G]GTCTGTCACTGTCCC	90678
rs755305509	snp	A/G			intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451038	GGCGAAACGCCCGGA[A/G]ACAAGCCTTACCCTA	90678
rs755308288	snp	A/G	2.48574e-05	0.00352535	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127467745	GTGTCTGCAGATGCT[A/G]AGCCTTGACGCCTCG	90678
rs755346698	snp	A/C	1.65908e-05	0.00288012	intron-variant	LRSAM1	GRCh38.p7	9:127480029	CTTCCCCGTGCAGTC[A/C]CCTGAGGAGCCGGGA	90678
rs755362254	snp	A/G	9.56343e-05	0.00691433	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127467789	CGCCGCGGGAGGTGT[A/G]TGGTGCCGGCACTGC	90678
rs755400290	snp	A/C			downstream-variant-500B	LRSAM1	GRCh38.p7	9:127503961	CGCTGCAGAGGTGCA[A/C]GTTGATTATGCATTT	90678
rs755422352	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127470287	CAGGAAACTTACAGT[C/T]ATGGTGGAAGGCACC	90678
rs755427350	snp	C/T	1.64757e-05	0.00287012	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127455600	GGAGCTTTTGCAACA[C/T]GCAAAGTTCTGCAGA	90678
rs755434238	snp	A/G	1.6513e-05	0.00287336	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127479978	TGCAGGACAATCAGA[A/G]GTTGGGCTCTGCTCC	90678
rs755475655	snp	C/G/T	3.43721e-05	0.00414549	utr-variant-5-prime, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451328	GGCATGGTGGAGGCG[C/G/T]CTGGTGTCGGATGAA	90678
rs755524280	snp	C/G	6.87309e-05	0.0058618	utr-variant-3-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127502935	CCTGGTCCTAGCCCT[C/G]CCTCGGCCACTGTGA	90678
rs755620315	snp	C/T	1.6489e-05	0.00287128	intron-variant	LRSAM1	GRCh38.p7	9:127473754	GTGTCTCTGGGTACC[C/T]CAGCTGTCTCCTCCC	90678
rs755648409	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127473217	AACTTTGAGTACATC[A/G]AAACTTACAACTTGT	90678
rs755655852	snp	G/T	1.6638e-05	0.00288422	intron-variant	LRSAM1	GRCh38.p7	9:127481159	GCTGGTGACTGCCAG[G/T]ACCTTTTATGATTTT	90678
rs755710185	snp	C/T	1.73471e-05	0.00294504	intron-variant	LRSAM1	GRCh38.p7	9:127481268	GCATTTTTTTTTTTT[C/T]TTTGAGACGGAGTCC	90678
rs755740466	snp	A/T			intron-variant	LRSAM1	GRCh38.p7	9:127472255	GTGAGACACCACGCC[A/T]GGCCAAGAAATAATT	90678
rs755766714	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127458920	GGGGGTGTGAGGTGG[C/T]CCCAGCCCCTCCTCA	90678
rs755784446	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127486212	AGCAAGCCAGCAGGT[A/G]GCGGAGCCAGGATTT	90678
rs755857059	snp	C/G	0.00030385	0.012322	intron-variant	LRSAM1	GRCh38.p7	9:127501155	GGAGGTAAGTCCGGG[C/G]CCCTCCCCACCCGCC	90678
rs755857174	snp	A/G	4.07756e-05	0.0045151	intron-variant	LRSAM1	GRCh38.p7	9:127492763	GACTCCTGCGCTGCC[A/G]CCAGCTCACGGTGGT	90678
rs755916665	snp	A/G	1.6507e-05	0.00287284	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127479433	GCGCCTGGAACTGGG[A/G]CAGCGGGAGCACACC	90678
rs755923233	snp	A/G	1.72291e-05	0.002935	utr-variant-5-prime, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451339	GGCGGCTGGTGTCGG[A/G]TGAACCCGGATTCGG	90678
rs755941676	snp	A/C/T	3.3022e-05	0.00406326	intron-variant	LRSAM1	GRCh38.p7	9:127461130	AAGTGCTGGGATTAC[A/C/T]GGCATAAGCCACTGC	90678
rs756006524	snp	C/T	1.64939e-05	0.0028717	intron-variant	LRSAM1	GRCh38.p7	9:127479363	CTGTGCTGACAGTCA[C/T]CAGGATCTGTGTCTT	90678
rs756043795	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127464053	GAACAGGGACTTCTC[C/T]ATTCATGGTGGCACG	90678
rs756115504	in-del	-/T	1.81524e-05	0.00301262	intron-variant	LRSAM1	GRCh38.p7	9:127492934	CAGCATCACACAGGC[-/T]ATTTGCTTTTCTTTA	90678
rs756130306	snp	C/T	1.74336e-05	0.00295237	intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127449576	CTACCTGTCCCCCCA[C/T]CCTCCTCTCCCGAAA	90678
rs756134400	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127478269	TTGCCTGGAGGTAGT[C/G]ATCATTAACTGATTA	90678
rs756149123	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127476856	AGTTTTGCATTTTGT[C/T]AGTAGAGACGGGGTT	90678
rs756166245	snp	A/G	1.67812e-05	0.0028966	intron-variant	LRSAM1	GRCh38.p7	9:127485854	AGGTAAGGAAGAGGA[A/G]TCCCAGGTGAGGGAG	90678
rs756188820	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127491851	GTGTGGCCCAGCACA[A/G]CCCTGCTGTGCAACT	90678
rs756218616	snp	C/T	1.72916e-05	0.00294032	intron-variant	LRSAM1	GRCh38.p7	9:127495961	CACGTTTCTGTCTTG[C/T]AGGAAGAGGGGATGG	90678
rs756254063	snp	A/G	1.65023e-05	0.00287244	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127485750	GCCGCCATGCAGCAG[A/G]TGCTGACTGAGAGCT	90678
rs756260380	snp	C/G	1.64757e-05	0.00287012	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127455589	AGATTCCATTTGGAG[C/G]TTTTGCAACATGCAA	90678
rs756276690	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127490332	TCAATTCCACATTGC[C/T]GGACATGAAGCTCAT	90678
rs756278772	snp	A/T	1.6473e-05	0.00286988	intron-variant	LRSAM1	GRCh38.p7	9:127455088	TGGGCTGTGAATTGG[A/T]TCTGTCCCGTTTTCT	90678
rs756282129	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127455345	GGGTTCACAATGGGG[A/G]CAGGGTGGGTGGGGC	90678
rs756293083	in-del	-/CT			intron-variant	LRSAM1	GRCh38.p7	9:127459672	AAGAGATTCTCATGC[-/CT]CTCAGCCTCCTGAGT	90678
rs756306033	snp	C/T	1.65578e-05	0.00287726	synonymous-codon, intron-variant, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127495401	TTGAACCAGAAGCCC[C/T]TGTCCTTGAAGCTGC	90678
rs756364990	snp	A/T	0.000197713	0.0099407	intron-variant	LRSAM1	GRCh38.p7	9:127454990	TTAAAAATTCTTTTT[A/T]TCCTTAGGCAAAAGA	90678
rs756393872	snp	C/T	4.89632e-05	0.00494765	utr-variant-3-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127502915	GTGCTGCCCGCCCAC[C/T]TGGGCCTGGTCCTAG	90678
rs756439043	snp	C/T			intron-variant, utr-variant-5-prime	LRSAM1	GRCh38.p7	9:127454169	AGAAAGACGCAGCCC[C/T]TGCCTCCGTGAAACT	90678
rs756460551	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127501752	AAAGAAAAAATCATC[C/T]TTTAAAAATTCATTA	90678
rs756461973	snp	C/T	5.2072e-05	0.00510228	intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451245	GGGCCGAGGGATGCT[C/T]CATCCCGCAGCCCCG	90678
rs756469742	snp	A/T	1.65094e-05	0.00287305	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127479966	TCCAGAAGCTGCTGC[A/T]GGACAATCAGAGGTT	90678
rs756492485	snp	A/G	1.66527e-05	0.00288549	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127479890	CAGCGCCACCTCAAC[A/G]CAGAGCGGCAGCGGC	90678
rs756499519	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127477449	ACTAAATAGAAGGAC[C/T]ATTCAAAAAATACCT	90678
rs756516100	snp	A/G	1.64743e-05	0.00287	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127462363	TGCTGGCTCACGTTC[A/G]AACCCTGGAGGTAAA	90678
rs756557269	snp	C/T	3.90297e-05	0.00441739	intron-variant	LRSAM1	GRCh38.p7	9:127489550	GGGTCCCTGGACCTG[C/T]TCTCTCAGAGACTTG	90678
rs756557431	snp	C/T	0.000144805	0.00850774	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127467756	TGCTGAGCCTTGACG[C/T]CTCGGCCATGGTCTA	90678
rs756632290	snp	C/T	1.66452e-05	0.00288484	intron-variant	LRSAM1	GRCh38.p7	9:127497338	GGATCCAGCCAGGTA[C/T]AAGCACAGCTCCAGC	90678
rs756667241	snp	A/T	0.00012484	0.00789965	intron-variant	LRSAM1	GRCh38.p7	9:127483033	CCTGTGAGTTTTGGG[A/T]TGGGGAGCTTGTGAG	90678
rs756668360	snp	A/G	2.92907e-05	0.00382681	intron-variant	LRSAM1	GRCh38.p7	9:127489435	GAGGGCTGGTGGTCT[A/G]TGTTGCAGAGCGCGA	90678
rs756674050	in-del	-/C	3.31444e-05	0.00407076	intron-variant	LRSAM1	GRCh38.p7	9:127491193	GTGAGTAAAAAAAAA[-/C]CCTGTCTCGTCTTCT	90678
rs756740139	snp	C/T	1.66405e-05	0.00288443	intron-variant	LRSAM1	GRCh38.p7	9:127481142	AGACAGGAAACAGGC[C/T]TGCTGGTGACTGCCA	90678
rs756768359	snp	G/T			intron-variant	LRSAM1	GRCh38.p7	9:127486139	GGACTGTATTGTTAT[G/T]AGCCCGATTTCACAA	90678
rs756804646	snp	G/T	1.65784e-05	0.00287905	synonymous-codon, intron-variant, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127491232	TAAGTTAATAGAAAC[G/T]GAGTTATTGCAGCTG	90678
rs756820785	snp	A/C	3.47917e-05	0.00417069	utr-variant-5-prime, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451363	GATTCGGGACGACCG[A/C]AGGAAGTTGCACCTT	90678
rs756830051	snp	A/G	1.65165e-05	0.00287367	intron-variant	LRSAM1	GRCh38.p7	9:127479982	GGACAATCAGAGGTT[A/G]GGCTCTGCTCCTCGG	90678
rs756840904	snp	C/T	1.72056e-05	0.00293301	utr-variant-5-prime, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451333	GGTGGAGGCGGCTGG[C/T]GTCGGATGAACCCGG	90678
rs756847437	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127481438	GTATTTTAGTAGAGA[C/T]GGGGTTTCACCGTGT	90678
rs756858558	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127484708	GAATGTGGGTTGTTT[C/T]CACTTTTTGACTCTT	90678
rs756880678	snp	A/G	1.65455e-05	0.00287619	splice-acceptor-variant	LRSAM1	GRCh38.p7	9:127501009	TGTCTGGTCCCCACA[A/G]AGCTGAAACCACCAA	90678
rs756929453	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127455844	TGGCTTCATGACTTG[C/G]GCAACTTCCTTAAAC	90678
rs756946389	snp	A/T			intron-variant	LRSAM1	GRCh38.p7	9:127496626	CCAGCAGGGTACATA[A/T]CATTATCATCATCTT	90678
rs756972573	snp	C/T	3.29957e-05	0.00406162	intron-variant	LRSAM1	GRCh38.p7	9:127479339	TCTGTGTCCTAACTC[C/T]CCCAGGGCCTGTGCT	90678
rs757019859	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127465431	GGCCACACATGGCTT[A/G]TAGCCAGCATCCTGG	90678
rs757094037	snp	A/C	1.65012e-05	0.00287234	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127459012	CTGCAGGTTCTAGAT[A/C]TCCACGATAATCAGC	90678
rs757101883	snp	A/G	1.65141e-05	0.00287346	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127485821	GCAGAACTTGGTCCA[A/G]CAGGCCTGTTCCAGG	90678
rs757124014	snp	C/T	1.6517e-05	0.00287372	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127485739	ATGTTCCCACAGCCG[C/T]CATGCAGCAGATGCT	90678
rs757135623	snp	C/T	8.25089e-05	0.00642243	intron-variant	LRSAM1	GRCh38.p7	9:127473955	AGGCAGCCTGCTGCA[C/T]GCATACATGTGTGTG	90678
rs757147459	snp	A/T			intron-variant	LRSAM1	GRCh38.p7	9:127462523	CTTGTAGAGAGGCCA[A/T]TGTGTGAACATTCGT	90678
rs757176553	in-del	-/TT	0.00243796	0.0348287	intron-variant	LRSAM1	GRCh38.p7	9:127481256	CAGGGGAGGGCAGCA[-/TT]TTTTTTTTTTTTTTG	90678
rs757194643	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127476445	CCCAGCTACGAGGGA[A/G]GCTAAGGTGGGAGGA	90678
rs757201364	in-del	-/CACCAT			intron-variant	LRSAM1	GRCh38.p7	9:127482564	TGCCCATTTCTCCAC[-/CACCAT]CACCATCACCATCAC	90678
rs757208185	snp	C/T	4.95651e-05	0.00497796	missense, intron-variant, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127495380	CTGATTCAGTATCAA[C/T]GGCTTTTGAACCAGA	90678
rs757301622	snp	C/T			synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127489500	GAAAGACCTGATGCA[C/T]CGGCAGATCAGGAGC	90678
rs757322928	snp	C/T	4.34452e-05	0.00466055	utr-variant-3-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127502908	CAGCTGAGTGCTGCC[C/T]GCCCACCTGGGCCTG	90678
rs757338372	snp	C/T			downstream-variant-500B	LRSAM1	GRCh38.p7	9:127503615	AAGGAGCCAGGAGTG[C/T]GCCGCACCTCAGTCG	90678
rs757370778	snp	C/G	1.72039e-05	0.00293285	intron-variant	LRSAM1	GRCh38.p7	9:127495269	CCATCATTGTTATTA[C/G]AGGTTTTATTACCAT	90678
rs757426906	snp	C/T	1.64741e-05	0.00286998	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127462358	GCAGATGCTGGCTCA[C/T]GTTCGAACCCTGGAG	90678
rs757428075	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127501605	GGCGTGGTGGTGGGC[A/G]CCTGTAAGCCCAGAT	90678
rs757438041	in-del	-/T			intron-variant	LRSAM1	GRCh38.p7	9:127456235	TGGAAGTTTTGTTTG[-/T]TTTTTTTTTTTTTTG	90678
rs757468849	snp	C/T			upstream-variant-2KB, intron-variant	RPL12, LRSAM1	GRCh38.p7	9:127452795	CTTTTCATCCCAAAG[C/T]CTGTGCTGCTCACCA	90678
rs757631013	snp	C/T	1.71328e-05	0.00292679	intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127449752	GTGTCCAGAGGTGAA[C/T]CACAGCCTTGAAACC	90678
rs757728861	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127474486	AGCTCCAGTCGAGGT[C/T]AGGTCTCCTGTTGTG	90678
rs757786881	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127494215	GCCCGGGAGGGCCAA[C/T]GACGGAAGGGAGCAG	90678
rs757816455	snp	C/T	1.69361e-05	0.00290994	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127496086	AATGAGCCCAGGGGA[C/T]CTGGCCAAGGTGGGC	90678
rs757832568	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127482865	CAAATCAAGGAGGCC[C/T]TCCTGGAGGAGGTGG	90678
rs757910414	snp	C/G	1.71264e-05	0.00292624	intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451261	CATCCCGCAGCCCCG[C/G]CCACAACCAGAGCAC	90678
rs757927845	in-del	-/G			intron-variant	LRSAM1	GRCh38.p7	9:127479756	AGGCAGGGTGGGAAA[-/G]GCCAGCCTCCTAACC	90678
rs757941401	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127483185	TGGGGTCAGCCTAGA[C/T]GTGGATGCAGAGTCC	90678
rs757957779	snp	A/G			utr-variant-3-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127503117	TCTGAATGGTCCTGG[A/G]GGCTGGGGCTGGAGA	90678
rs757966337	snp	A/C	2.44651e-05	0.00349742	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127489491	CCAGGTGAAGAAAGA[A/C]CTGATGCATCGGCAG	90678
rs757980176	in-del	-/GCA			intron-variant	LRSAM1	GRCh38.p7	9:127455657	AGAGACTTTCTTGTT[-/GCA]TGTCTGCTTGTTTGA	90678
rs757987823	in-del	-/G	5.03622e-05	0.00501782	intron-variant	LRSAM1	GRCh38.p7	9:127479835	CCCCTACCTCCGGCT[-/G]CAGGAGCAGTCCCGG	90678
rs758039190	snp	A/C/G	8.23725e-05	0.00641722	intron-variant	LRSAM1	GRCh38.p7	9:127462388	GGTAAATGGGAAGCT[A/C/G]TTCTTGCCTGGGGTG	90678
rs758053163	in-del	-/G			intron-variant	LRSAM1	GRCh38.p7	9:127481049	TCAGTAACTGGCTAA[-/G]AACCCAGAGCTTCAA	90678
rs758071164	snp	A/G	1.64966e-05	0.00287194	intron-variant	LRSAM1	GRCh38.p7	9:127473949	AAGACAAGGCAGCCT[A/G]CTGCACGCATACATG	90678
rs758094270	snp	A/C	1.65225e-05	0.00287419	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127485736	CTCATGTTCCCACAG[A/C]CGCCATGCAGCAGAT	90678
rs758212710	snp	G/T			intron-variant	LRSAM1	GRCh38.p7	9:127461796	AGGAGCGCTCTGCTC[G/T]CCACACCCAGCTCTC	90678
rs758262867	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127491433	GGGCAGAGCTCCTCT[A/G]TGGCTGTGACACCAG	90678
rs758268411	snp	A/G	6.03045e-05	0.00549078	intron-variant	LRSAM1	GRCh38.p7	9:127483040	GTTTTGGGATGGGGA[A/G]CTTGTGAGCACGCTG	90678
rs758288782	snp	C/T	5.58114e-05	0.00528229	intron-variant	LRSAM1	GRCh38.p7	9:127492940	TCACACAGGCATTTG[C/T]TTTTCTTTAACAGAC	90678
rs758290295	snp	A/T	3.37279e-05	0.00410644	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127492839	GGGCCCTCAGCTCCC[A/T]GCTCCAGCAGCTGCT	90678
rs758347382	in-del	-/TAT			intron-variant	LRSAM1	GRCh38.p7	9:127499539	CTGTCTAAAAAAAAA[-/TAT]ATATATATATATATA	90678
rs758352707	snp	A/G	1.98167e-05	0.00314769	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127502826	GCTGCCAGCAGTGCT[A/G]CCAGCCACTGCGCAC	90678
rs758363472	snp	C/G	3.47072e-05	0.00416562	intron-variant	LRSAM1	GRCh38.p7	9:127489404	TGCAGGGAAAAGTGT[C/G]GGCACGGCCCCTGCT	90678
rs758382647	snp	A/G	1.6492e-05	0.00287154	intron-variant	LRSAM1	GRCh38.p7	9:127462233	GGGGTGTTGAGCTGT[A/G]CTATTGGGGTCTCTG	90678
rs758393258	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127499185	TGAGACCAGCCTGGG[C/T]GACATAGGGAGACCC	90678
rs758399565	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127501509	GGCCAAGGCAGGTGG[A/G]TCACCTGAGGTCAGG	90678
rs758449842	snp	A/C			intron-variant	LRSAM1	GRCh38.p7	9:127488413	ATTACGGGCACCCAC[A/C]AACACGCCCAACTAA	90678
rs758506310	snp	A/C			intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127450913	CTCTTCTCGAAACAG[A/C]ACAGAGCGCGAGGCG	90678
rs758506472	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127467342	ATGTGCCATCCACTG[C/T]GCGTGTCCCCAGGAG	90678
rs758628826	snp	G/T	1.65195e-05	0.00287393	intron-variant	LRSAM1	GRCh38.p7	9:127489402	GCTGCAGGGAAAAGT[G/T]TGGGCACGGCCCCTG	90678
rs758674373	snp	A/G	1.66571e-05	0.00288587	intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127449605	AACCAAGCACAAGCA[A/G]ATACCTGGGCCTGTC	90678
rs758682465	snp	C/T	1.6793e-05	0.00289763	intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127449724	CTAGAAATAAAGGCA[C/T]GTAATCAACATGGTG	90678
rs758684371	in-del	-/TTC	1.75705e-05	0.00296394	intron-variant	LRSAM1	GRCh38.p7	9:127495919	GTTGTAAACAGTGGG[-/TTC]TTTTCTTCCTTCCTG	90678
rs758692752	snp	C/T	1.64808e-05	0.00287057	intron-variant	LRSAM1	GRCh38.p7	9:127455635	GGTAAGATGGAGCTT[C/T]ATCTTCAGAGACTTT	90678
rs758772061	snp	A/C			intron-variant	LRSAM1	GRCh38.p7	9:127458462	GCTTGTGCTTGTAAT[A/C]CCAGCTACTTGGGAG	90678
rs758774140	snp	C/G/T	0.000316569	0.0125774	intron-variant	LRSAM1	GRCh38.p7	9:127457297	TCAGCCCAGCATGGC[C/G/T]GCACATCTCTCCACA	90678
rs758777482	snp	C/G	9.06659e-05	0.00673237	intron-variant	LRSAM1	GRCh38.p7	9:127467877	TGAGGAACTATGACC[C/G]CCATGGCCACCCTGT	90678
rs758793220	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127492181	TCCATAAGATGGCAG[C/T]GGTCCTCCAGGCCCA	90678
rs758810654	snp	A/G	3.56856e-05	0.00422392	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127487727	GTCGTGGCAGCAAAT[A/G]GATCAGAACAAAGCC	90678
rs758812956	snp	A/G	1.65203e-05	0.002874	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127459050	CCTTCCTGACGATCT[A/G]GGGCAGCTGACTGCC	90678
rs758867006	snp	A/C/T	0.00031943	0.0126344	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127467804	GTGGTGCCGGCACTG[A/C/T]GGCCATCTTGCAGTT	90678
rs758880511	snp	A/C			intron-variant	LRSAM1	GRCh38.p7	9:127497027	TCAGTTTCCCCCCAA[A/C]CCCTGCCACACTGAT	90678
rs758898673	snp	C/T	3.36939e-05	0.00410436	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127496059	CCGCCTCTCACTGGA[C/T]CTGCTGAGCCAAATG	90678
rs758916865	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127462115	GAACTGGAACTCCAC[C/G]TTCTTGAGCCTAGGA	90678
rs759004544	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127472446	CAGGAGTTCGAGACC[A/G]CCTTTACCAACATGC	90678
rs759029105	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127477529	CCGAGTCGGGTGGAT[C/G]CTTGAGCTCAGGAGT	90678
rs759062514	snp	A/C			intron-variant	LRSAM1	GRCh38.p7	9:127464492	GTGGCTTGTGTGTAC[A/C]GCCAGGAACTAAAAG	90678
rs759065503	snp	A/G	1.64727e-05	0.00286986	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127455031	GATGACATTCTCGAC[A/G]TCTCTAAATGTGAGC	90678
rs759109925	snp	A/G	0.000131941	0.00812116	intron-variant	LRSAM1	GRCh38.p7	9:127473935	TTAGAGTGGCAGGTA[A/G]GACAAGGCAGCCTGC	90678
rs759109966	snp	A/G	1.64936e-05	0.00287168	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127485795	ATCCAGATGGCCTAC[A/G]AATCTCAGAGGCAGA	90678
rs759126418	snp	C/T	4.96479e-05	0.00498212	intron-variant	LRSAM1	GRCh38.p7	9:127485718	CCACTCAGCTGTCCC[C/T]ACCTCATGTTCCCAC	90678
rs759150632	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127490829	AACAGCGATGCGAGG[A/G]ACAAGAGAACTTGAC	90678
rs759232309	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127467930	CAGAGACAGAAATGG[C/T]CACAGTGCCTACCTG	90678
rs759239338	snp	A/G	1.6476e-05	0.00287014	intron-variant	LRSAM1	GRCh38.p7	9:127462415	GGTGCTCTCTGGCCT[A/G]CCCACCTCCCCTCTC	90678
rs759310014	snp	A/G			intron-variant, utr-variant-5-prime	LRSAM1	GRCh38.p7	9:127453677	CAGGAAAAGGATAAT[A/G]CCAAGGCCTCACTAT	90678
rs759312530	snp	C/T	1.85555e-05	0.00304588	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127502807	AACTGTGGCCACGTC[C/T]GCTGCTGCCAGCAGT	90678
rs759326900	snp	C/T	1.64765e-05	0.00287019	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127462319	TACCCTCAACATCAG[C/T]GGAAACGAGATCCAG	90678
rs759327809	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127502519	GTGAAACCCCATCTC[C/T]ACTAAAAATACAAAA	90678
rs759373322	snp	A/C/T	3.35038e-05	0.0040928	missense, stop-gained, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127479908	GAGCGGCAGCGGCTG[A/C/T]AGGAGCAGCTGAAGC	90678
rs759417653	snp	A/T			intron-variant	LRSAM1	GRCh38.p7	9:127501363	CTTTTTGTTCCTACT[A/T]AATAAATACATTAGG	90678
rs759431844	snp	C/G/T	0.000341174	0.0130572	intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127450842	GTCTGTGCAGAGGGA[C/G/T]CCCCGAGCCACAGCC	90678
rs759441679	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127467038	GCTGTTGTAACCAAG[C/T]GAGTTATAGAGAAAC	90678
rs759441695	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127482088	GGAAAACATAACATA[C/T]TGCTAATGGAAAAAG	90678
rs759449818	in-del	-/TAGC			intron-variant	LRSAM1	GRCh38.p7	9:127455947	TAAATGAGTGGTAGA[-/TAGC]TAGATAGAGATAGAA	90678
rs759453124	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127494622	TAGAACAGTACTCAA[C/T]GAAGAGTTATCGAAT	90678
rs759591552	snp	A/G	0.000143944	0.0084824	synonymous-codon, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127450776	GGCAGAAGTGGCACC[A/G]ACTTCACCTCCGGTG	90678
rs759626530	snp	A/G	4.24791e-05	0.00460844	intron-variant	LRSAM1	GRCh38.p7	9:127487791	CCAGAGCCTGAGGGT[A/G]GGAGCTCAGGAGGGA	90678
rs759667401	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127493946	AGAGACCAGCTGCTT[C/T]TGGAGCCCTGAACAA	90678
rs759739563	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127460155	CAGGCGCCCACCACT[A/G]TGCCTGGCTAATTTT	90678
rs759751440	snp	C/T	3.37644e-05	0.00410866	utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127454510	GGGTCCTAAAGATCG[C/T]TCTGGGAAAAGGGAA	90678
rs759853952	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127487256	CAGGTTCTTGTGCCC[A/G]AGTCAAGGGCTGCTC	90678
rs759866619	snp	A/G	4.99671e-05	0.00499811	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127481218	TTTTGAAATCGCTGG[A/G]AAATGAAAGGTAAGT	90678
rs759938196	in-del	-/T	1.64749e-05	0.00287005	intron-variant	LRSAM1	GRCh38.p7	9:127478918	CTCTTGACCACTGTC[-/T]TTTTTTTCCTCCCAG	90678
rs759995336	snp	A/C	1.78634e-05	0.00298854	intron-variant	LRSAM1	GRCh38.p7	9:127491339	CTTCACGTGGTGAGA[A/C]CCCCACCTGGTGCTC	90678
rs760000442	snp	C/T	3.30017e-05	0.00406199	intron-variant	LRSAM1	GRCh38.p7	9:127461273	GTAGGGACCAAGAAG[C/T]CGTGTCCGTGTGACC	90678
rs760017824	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127498414	GTTGGGGTCACCCCC[A/G]GCAGACAAGCCTCAC	90678
rs760040162	snp	A/C	3.46356e-05	0.00416132	intron-variant	LRSAM1	GRCh38.p7	9:127454603	CAGATGTGTTTGGTG[A/C]GGGAAAGTGGGTTTC	90678
rs760074620	snp	C/T	7.6365e-05	0.00617873	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127483013	CCTGCGGCGACGTGA[C/T]GTTGCCTGTGAGTTT	90678
rs760075540	snp	C/T			intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127450153	ACGGCCAAGGAAGAA[C/T]AGTTAAGATACAGGT	90678
rs760104002	snp	C/G	1.66147e-05	0.0028822	intron-variant	LRSAM1	GRCh38.p7	9:127497244	CTGCACTTCCTTGAA[C/G]TGTCACAGGTGGGCG	90678
rs760132139	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127489106	TGGTTAAGTGGGGCT[C/T]GGGAGCTGGATAGGC	90678
rs760156426	snp	C/T			intron-variant, utr-variant-5-prime	LRSAM1	GRCh38.p7	9:127453507	CATGATGTAGTTGAG[C/T]TCCCTGAGGTCCTGG	90678
rs760173857	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127489887	CGGCGCAGGCCCCAG[C/T]GCTCCTACAGCTCAG	90678
rs760181103	in-del	-/G			intron-variant	LRSAM1	GRCh38.p7	9:127487399	CAGGCATCCACTTCC[-/G]GGGGGGTGCTGGGGA	90678
rs760224025	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127500902	GAGCAGAGGCTCCCC[C/G]ACCCTCCAGCTCACT	90678
rs760242559	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127468304	TCATTAGGCTGCAGG[A/G]AGGAGAAGGGATTGG	90678
rs760321710	snp	A/G	3.38885e-05	0.0041162	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127492887	GAGAGGAAGAGCTCC[A/G]GGAAATCCTGGTATG	90678
rs760403428	snp	A/G			upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	RPL12, LRSAM1	GRCh38.p7	9:127451659	CTAGCTGTTTCCCAT[A/G]TTCCTTTATCGTGAG	90678
rs760435393	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127490442	CTGGCTATGGGGTCT[A/G]ACCCCCACCCCTGCC	90678
rs760457324	snp	C/T	6.879e-05	0.00586432	intron-variant	LRSAM1	GRCh38.p7	9:127479538	TAGGGTCCAGCCTGG[C/T]TGCATCCCCCAGCCA	90678
rs760485483	snp	A/C	1.72853e-05	0.00293979	intron-variant	LRSAM1	GRCh38.p7	9:127496129	CATGGAGGGGAGGGG[A/C]ACGCAAGGCCGCTGT	90678
rs760491120	snp	A/G	6.28911e-05	0.00560728	intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127450720	AATGCCCCTTGGAGG[A/G]GATAACGTACCAGAC	90678
rs760551844	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127480431	CTGGGGAGACATGGC[A/G]CCAGAAAAGCCTGAG	90678
rs760563840	snp	A/G	1.77871e-05	0.00298215	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127487692	ATGGCCGAAATGGAT[A/G]AACGATTCCAGCAGA	90678
rs760574030	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127493556	TATTGTTGAGTATGT[A/G]GATTACTTCTGGTTT	90678
rs760581208	snp	A/C	1.65293e-05	0.00287479	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127457370	CCCAAATCCTGCAGC[A/C]TCCTGAGTCTGGCAA	90678
rs760713185	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127484968	ACCTGCCACCATGCC[C/T]GGCTAATTTTTGTAT	90678
rs760792213	snp	C/T	6.45849e-05	0.00568228	intron-variant	LRSAM1	GRCh38.p7	9:127467848	AAAGCCAGGCCGCTG[C/T]CTCCTCCCCTCATTG	90678
rs760847709	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127457747	CCTGCTGACTGTGAG[C/T]TCCTCCCCGGATGGG	90678
rs760852578	snp	A/G	8.65898e-05	0.00657932	utr-variant-5-prime, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451354	ATGAACCCGGATTCG[A/G]GACGACCGAAGGAAG	90678
rs760863378	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127457025	TTTTCCACGTGAAGA[C/T]GCTGGTGCTGGGAAG	90678
rs760866621	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127485879	AGGGAGCTGGGGGAG[C/G]TGGCTCAGGGCCCAA	90678
rs760944483	in-del	-/GCGGAAACCCAGTGAGGAGGC	0.000150214	0.00866513	cds-indel, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127454547	GCTCTTCTTCCGGAA[-/GCGGAAACCCAGTGAGGAGGC]GCGGAAACCCAGTGA	90678
rs760948810	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127475553	GTAATCAGAGGAGAG[A/G]CATGTTAAGTTAAAA	90678
rs760951204	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127471244	AACATTTTGGGAGGC[C/G]AAGGCGGGTGGATCG	90678
rs760989075	snp	C/T			intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127450015	AAAATACTAGGCTCC[C/T]ATGTCAGACCACCCA	90678
rs760992826	snp	G/T	1.72883e-05	0.00294004	intron-variant	LRSAM1	GRCh38.p7	9:127491322	TCCCTGCCCCTGCCC[G/T]CCTTCACGTGGTGAG	90678
rs761099240	snp	A/G	1.7024e-05	0.00291749	intron-variant	LRSAM1	GRCh38.p7	9:127497381	GGGCTCCAGCCGTAT[A/G]TGTGGGCTCTGGTGG	90678
rs761128196	snp	C/T	1.65351e-05	0.00287528	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127459064	TGGGGCAGCTGACTG[C/T]CCTCCAGGTAAGGCT	90678
rs761151812	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127483952	CAGGCGTGAGCCACC[C/G]TGCCTGGTCTTCATT	90678
rs761189491	in-del	-/GC	4.97996e-05	0.00498972	intron-variant	LRSAM1	GRCh38.p7	9:127473974	TACATGTGTGTGTGT[-/GC]GTGTGCATGTATGTG	90678
rs761222406	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127496226	CCCAGGGCCACCTTG[C/T]TTCCAGATGGCCAGA	90678
rs761235141	snp	C/T	1.69576e-05	0.00291179	intron-variant	LRSAM1	GRCh38.p7	9:127479530	CCGCCTGCTAGGGTC[C/T]AGCCTGGCTGCATCC	90678
rs761243064	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127463130	CTTGAACCCGGGAGG[C/T]GGAGATTGCAGTGAG	90678
rs761287467	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127473181	ACGTGACTGTATCCT[C/T]CCCATGAGGGGAAAG	90678
rs761364421	snp	A/C			upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	RPL12, LRSAM1	GRCh38.p7	9:127451552	GCTGGCAAGCAGGGC[A/C]CCGCGGTGCGCTGAA	90678
rs761388790	snp	A/G	5.27653e-05	0.00513614	intron-variant	LRSAM1	GRCh38.p7	9:127502749	CCGGTAGGGCCAGCC[A/G]CATGCTCCCGCTCTC	90678
rs761390274	in-del	-/CCTGGG	9.68054e-05	0.00695653	utr-variant-3-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127502913	AGTGCTGCCCGCCCA[-/CCTGGG]CCTGGGCCTGGTCCT	90678
rs761449900	snp	A/C	3.50349e-05	0.00418524	intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127449573	TTGCTACCTGTCCCC[A/C]CACCCTCCTCTCCCG	90678
rs761453114	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127466776	CCAGCACTTTGGGAG[A/G]CGGGCGAATTGCTTG	90678
rs761535879	snp	A/G	1.64749e-05	0.00287005	splice-acceptor-variant	LRSAM1	GRCh38.p7	9:127455574	TCTTTATCTTATCTT[A/G]GATTCCATTTGGAGC	90678
rs761552519	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127465417	ATGTAACCATAAATG[A/G]CCACACATGGCTTGT	90678
rs761586126	snp	A/G	3.30142e-05	0.00406276	synonymous-codon, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127449655	CACTGTAATCCTCAG[A/G]CCCTTCCAGTCACCC	90678
rs761604510	snp	G/T	0.000280378	0.0118368	intron-variant	LRSAM1	GRCh38.p7	9:127455669	GTTGCATGTCTGCTT[G/T]TTTGAACCCACAAGG	90678
rs761606752	snp	A/C			intron-variant	LRSAM1	GRCh38.p7	9:127479269	GAGTGGGGGTTGCTC[A/C]GCATGAAGACCTGGA	90678
rs761611795	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127485282	TAAAAAGAACAGGCC[A/G]GGCGCAGTGGCTCAC	90678
rs761619043	in-del	-/GAGGCTGGTG			intron-variant	LRSAM1	GRCh38.p7	9:127475257	AAATATTGGGAGGCC[-/GAGGCTGGTG]GATCACTTGAGGCCA	90678
rs761638089	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127456527	TGAGCCACCACGCCC[A/G]GTCTGTGCTGGAAGT	90678
rs761659187	snp	G/T	1.69522e-05	0.00291132	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127496033	CACTACCTGCCCATC[G/T]TTGCGCACCACCGCC	90678
rs761696500	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127492675	TAGCTTTGTCCCCCA[A/G]CGCAGCCTGGAGGCA	90678
rs761729765	snp	A/C			intron-variant	LRSAM1	GRCh38.p7	9:127470843	GTGTTCACCTTTAAA[A/C]ATTCATCAAGCTCTG	90678
rs761734305	in-del	-/AA			intron-variant	LRSAM1	GRCh38.p7	9:127499530	GCAAGACCCTGTCTA[-/AA]AAAAAAAATATATAT	90678
rs761882657	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127455212	CGTCCAAAATAATTG[A/G]AGATGATCCTTTGGC	90678
rs761890031	snp	A/G	6.92561e-05	0.00588415	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127467778	CATGGTCTACCCGCC[A/G]CGGGAGGTGTGTGGT	90678
rs761964249	snp	C/G	1.68769e-05	0.00290485	intron-variant	LRSAM1	GRCh38.p7	9:127491303	CACTCCAGGTATGTA[C/G]GGCTCCCTGCCCCTG	90678
rs761971578	in-del	-/TG	0.00107143	0.0231207	intron-variant	LRSAM1	GRCh38.p7	9:127473963	TGCTGCACGCATACA[-/TG]TGTGTGTGTGCGTGT	90678
rs762000052	snp	A/G	8.25757e-05	0.00642503	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127479948	AGAACATTTCCAGCC[A/G]GATCCAGAAGCTGCT	90678
rs762024505	in-del	-/G	3.4308e-05	0.00414159	utr-variant-5-prime, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451321	CTTCGGCGGCATGGT[-/G]GAGGCGGCTGGTGTC	90678
rs762065328	snp	A/G	1.69928e-05	0.00291481	intron-variant	LRSAM1	GRCh38.p7	9:127497374	CCAGGCAGGGCTCCA[A/G]CCGTATGTGTGGGCT	90678
rs762072180	snp	C/G	1.74293e-05	0.00295201	intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451234	CACGCGCGGCAGGGC[C/G]GAGGGATGCTCCATC	90678
rs762211656	snp	A/T			intron-variant	LRSAM1	GRCh38.p7	9:127461774	ACTGCACAGGCGCCT[A/T]ACCCGCAGGAGCGCT	90678
rs762242062	snp	A/G	3.29592e-05	0.00405938	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127473925	AAGGGAGGAGTTAGA[A/G]TGGCAGGTAAGACAA	90678
rs762243640	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127463387	AGGAGGTAGGGAGCC[A/G]TTGGGATGGGGGTTC	90678
rs762299534	snp	A/C			intron-variant	LRSAM1	GRCh38.p7	9:127460428	CAGCACCACTGCCGG[A/C]CTGAGGCCTTGGGTG	90678
rs762301665	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127476036	TGAGCCACCACACCC[A/G]CCAGATGTCAAAAAT	90678
rs762307490	snp	A/C	1.6617e-05	0.00288239	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127497320	AACTGCTGGATGCAG[A/C]CAGGATCCAGCCAGG	90678
rs762347168	snp	C/G	4.9579e-05	0.00497866	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127501052	TCACCCCTACGGCCC[C/G]CCAGGAGCCTCCTGA	90678
rs762371077	in-del	-/AG			intron-variant	LRSAM1	GRCh38.p7	9:127476531	CCCATCCTGAGTAAC[-/AG]AACTAGACCCTATCT	90678
rs762386227	snp	C/T			intron-variant, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127487661	GAATGAATGAATTTG[C/T]TGTCTTTCTGGCAGC	90678
rs762394174	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127463422	TTATCCAGGCCAGGG[A/G]AGTTCTATAGGCTAG	90678
rs762570500	snp	G/T	1.64808e-05	0.00287057	intron-variant	LRSAM1	GRCh38.p7	9:127478995	ACCCTTCTGTCACTC[G/T]TTTCTCATTAAAGAT	90678
rs762630109	snp	A/G	1.64985e-05	0.0028721	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127485806	CTACGAATCTCAGAG[A/G]CAGAACTTGGTCCAG	90678
rs762663263	snp	C/T	3.54956e-05	0.00421266	intron-variant	LRSAM1	GRCh38.p7	9:127467691	AAATCGTGTGGTCTC[C/T]GGTTGCGTTGGTAGC	90678
rs762666237	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127477666	GAGGTGGGAGGATCA[C/T]TAGAGCCCAGGAGGT	90678
rs762674170	in-del	-/ATC			intron-variant	LRSAM1	GRCh38.p7	9:127496631	AGGGTACATATCATT[-/ATC]ATCATCTTTCAGTTG	90678
rs762712712	snp	A/G	6.60513e-05	0.00574641	synonymous-codon, intron-variant, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127495352	AAGTGAAACCAGGCA[A/G]GAAAATTACTGGCTG	90678
rs762713959	snp	A/G	1.64749e-05	0.00287005	intron-variant	LRSAM1	GRCh38.p7	9:127455547	ACTGGCAGGAGGGGA[A/G]ACACTTACTCTTCTT	90678
rs762731732	snp	C/T	3.29451e-05	0.00405851	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127455047	TCTCTAAATGTGAGC[C/T]CTCAGAGGTAAACTG	90678
rs762747415	snp	C/G			utr-variant-3-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127503217	CTGTCTTGACTGAAG[C/G]CCACCGCCCCTGCAG	90678
rs762785076	snp	C/T	0.000115303	0.00759199	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127455027	GGCAGATGACATTCT[C/T]GACATCTCTAAATGT	90678
rs762787803	snp	C/T	6.98971e-05	0.00591132	intron-variant	LRSAM1	GRCh38.p7	9:127495938	TTTCTTCCTTCCTGC[C/T]CATGGTACACGTTTC	90678
rs762796023	snp	C/T	2.33833e-05	0.00341923	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127467768	ACGCCTCGGCCATGG[C/T]CTACCCGCCGCGGGA	90678
rs762832391	snp	C/T	1.65252e-05	0.00287443	synonymous-codon, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127449625	CTGGGCCTGTCTGTT[C/T]TGAATGGTCAGTTTC	90678
rs762870327	snp	G/T			missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127478940	TCCTCCCAGAACAGG[G/T]TCTCAGACTATGAGA	90678
rs762873320	snp	C/T			intron-variant, utr-variant-5-prime	LRSAM1	GRCh38.p7	9:127453921	AAGATGTGGCCCCTG[C/T]CCCCATGGAACTCCA	90678
rs762932995	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127493308	CTCAAACGATCTGTC[C/T]GCCTTGGCCTCCGAA	90678
rs762964267	snp	A/G	1.69135e-05	0.002908	intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127450810	CTCAGGTATACTGGG[A/G]GAAAAGAAGAGTTAG	90678
rs762965206	snp	A/C			intron-variant	LRSAM1	GRCh38.p7	9:127468960	GGAGCAAGACTCCAA[A/C]AAAGCAATACCCTAT	90678
rs763021099	snp	C/G	1.74266e-05	0.00295178	intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451230	TTTGCACGCGCGGCA[C/G]GGCCGAGGGATGCTC	90678
rs763061995	snp	A/T	1.66896e-05	0.00288869	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127479868	GGAGCAGGGCCTGAG[A/T]GAGCACCAGCGCCAC	90678
rs763127080	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127482443	CCACCGCACCCGGCC[A/G]TGTGACTATTTGTGA	90678
rs763155167	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127494031	ACTGCCATCTCCTAC[A/G]CATCAGGTTACTTTG	90678
rs763160989	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127460274	AAGTGCTGGGATTAC[A/G]GGTGTTAGCCACCGT	90678
rs763189614	in-del	-/G	1.72731e-05	0.00293875	intron-variant	LRSAM1	GRCh38.p7	9:127501152	ACGGGAGGTAAGTCC[-/G]GGGCCCTCCCCACCC	90678
rs763191697	in-del	CAAGGACA/GCAGAGCATGTTG			intron-variant	LRSAM1	GRCh38.p7	9:127458434	CAAAAAAAAACACCA[CAAGGACA/GCAGAGCATGTTG]GCTTGTGCTTGTAAT	90678
rs763207830	in-del	-/G	1.69069e-05	0.00290743	intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127450698	AAGTGAAACAAATGT[-/G]GAAAAAAATGCCCCT	90678
rs763219661	snp	G/T			intron-variant	LRSAM1	GRCh38.p7	9:127461642	TCCTGAGGAGTCCAC[G/T]GGGCAGGCTGAGGGC	90678
rs763326318	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127474692	ACCAAATGCTACTCA[C/T]TGTCTGGGACACACA	90678
rs763390117	snp	C/T	0.000264669	0.0115006	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127483002	GAGACTGAGAGCCTG[C/T]GGCGACGTGACGTTG	90678
rs763392918	snp	A/T			intron-variant	LRSAM1	GRCh38.p7	9:127487031	CTACTAAAAATACAA[A/T]CAATTAGCCAAACGT	90678
rs763481860	snp	A/G	1.68474e-05	0.00290231	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127492876	GAAGCAGCAGCGAGA[A/G]GAAGAGCTCCGGGAA	90678
rs763505762	snp	A/C			intron-variant, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127487611	ATCTCCTCCAAGGGG[A/C]CTGGCACATAGTAGG	90678
rs763518698	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127463057	AAGAAATTATCCAGG[C/G]GTGGTGGTGCGCACC	90678
rs763598737	in-del	-/T	3.59991e-05	0.00424243	intron-variant	LRSAM1	GRCh38.p7	9:127481254	CCAGGGGAGGGCAGC[-/T]ATTTTTTTTTTTTTT	90678
rs763601883	snp	C/G	1.67444e-05	0.00289343	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127454530	GGAAAAGGGAAGGAT[C/G]CCGCTCTTCTTCCGG	90678
rs763621387	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127470770	GACACAAAGGAATAT[A/G]TGCTCTTATCAGTCA	90678
rs763624714	in-del	-/A			intron-variant	LRSAM1	GRCh38.p7	9:127491183	GTGGTTAATGTGAGT[-/A]AAAAAAAAACCCTGT	90678
rs763643105	snp	G/T	1.64825e-05	0.00287071	intron-variant	LRSAM1	GRCh38.p7	9:127479008	TCTTTTCTCATTAAA[G/T]ATCTCAACTCAACTC	90678
rs763654096	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127496555	TAGCACCTGCACGTG[C/T]GGGGCACCATTTTAA	90678
rs763686785	snp	C/G	3.55809e-05	0.00421772	intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127449564	CCCAGAGGGTTGCTA[C/G]CTGTCCCCCCACCCT	90678
rs763709735	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127465279	CACGATGAGAATGCT[C/G]TATGATCTGTGCAGC	90678
rs763765654	snp	C/G	1.64749e-05	0.00287005	intron-variant	LRSAM1	GRCh38.p7	9:127455555	GAGGGGAGACACTTA[C/G]TCTTCTTTATCTTAT	90678
rs763793736	snp	G/T	1.64741e-05	0.00286998	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127478939	TTCCTCCCAGAACAG[G/T]TTCTCAGACTATGAG	90678
rs763798037	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127463553	CCTGTGTACATGTCC[A/G]GGTCCAAATTCCCTC	90678
rs763828049	snp	C/T	5.24031e-05	0.00511848	intron-variant	LRSAM1	GRCh38.p7	9:127495939	TTCTTCCTTCCTGCT[C/T]ATGGTACACGTTTCT	90678
rs763830624	in-del	-/C	0.000474685	0.0153986	intron-variant	LRSAM1	GRCh38.p7	9:127501155	GAGGTAAGTCCGGGG[-/C]CCCTCCCCACCCGCC	90678
rs763882034	in-del	-/TC			intron-variant	LRSAM1	GRCh38.p7	9:127497098	TGCCGCACTGCCTCA[-/TC]TCCTGACCGTGGGCC	90678
rs763903913	snp	C/T	3.30437e-05	0.00406457	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127485737	TCATGTTCCCACAGC[C/T]GCCATGCAGCAGATG	90678
rs763963537	in-del	-/AC			intron-variant	LRSAM1	GRCh38.p7	9:127457953	CTGTATGTGTTCACT[-/AC]AGATGCTTTCTTTCT	90678
rs763970960	snp	A/T			intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127449756	CCAGAGGTGAACCAC[A/T]GCCTTGAAACCTGCC	90678
rs763980228	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127476417	GCCAGGCATAGTGGC[A/G]CGTGCCTGTGGTCCC	90678
rs763989536	snp	C/T	1.65151e-05	0.00287355	synonymous-codon, intron-variant, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127495365	CAGGAAAATTACTGG[C/T]TGATTCAGTATCAAC	90678
rs764027836	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127501609	TGGTGGTGGGCGCCT[A/G]TAAGCCCAGATACTT	90678
rs764036829	snp	A/G	3.53964e-05	0.00420677	intron-variant	LRSAM1	GRCh38.p7	9:127467692	AATCGTGTGGTCTCC[A/G]GTTGCGTTGGTAGCG	90678
rs764056367	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127501545	GAGGCCAGCCTGGCC[A/G]ACATGGTAAAACTCC	90678
rs764062904	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127468516	TCAGAATGCAACCAA[C/G]ACACACATGCCTATG	90678
rs764077354	snp	A/C	3.44881e-05	0.00415245	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127502893	CCGCATCTACCACAG[A/C]AGCTGAGTGCTGCCC	90678
rs764119919	snp	A/C			utr-variant-3-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127503249	AGCTTGGGTCCTCAT[A/C]TGGGGGCCATGCACA	90678
rs764144965	snp	G/T	1.74224e-05	0.00295142	intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451231	TTGCACGCGCGGCAG[G/T]GCCGAGGGATGCTCC	90678
rs764152867	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127482519	CAAAAACATTCTGCC[A/G]GTTTACACTCCTCTC	90678
rs764158379	snp	A/G	1.65493e-05	0.00287652	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127479931	GCTGAAGCAGACGGA[A/G]CAGAACATTTCCAGC	90678
rs764243243	snp	C/T	9.90524e-05	0.00703679	intron-variant	LRSAM1	GRCh38.p7	9:127458983	TCACTTGGAGACTCA[C/T]AGGGGTCTTTCTTCT	90678
rs764321843	snp	A/G	1.66574e-05	0.0028859	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127479879	TGAGTGAGCACCAGC[A/G]CCACCTCAACGCAGA	90678
rs764321894	snp	C/G	2.85238e-05	0.00377638	intron-variant	LRSAM1	GRCh38.p7	9:127489536	GAGCGCTGGGGCTGG[C/G]GTCCCTGGACCTGCT	90678
rs764328571	snp	A/G	0.000301079	0.0122658	intron-variant	LRSAM1	GRCh38.p7	9:127497207	CTCACACCATTTAGC[A/G]GGCTCCCGCCCAGGC	90678
rs764331245	snp	A/G	5.05063e-05	0.005025	intron-variant	LRSAM1	GRCh38.p7	9:127457396	GGCAACCATCAAGGT[A/G]CTGGGCCCTCCTCCC	90678
rs764391717	snp	C/T	1.66037e-05	0.00288125	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127497307	CGGAGAGTCCAGGAA[C/T]TGCTGGATGCAGCCA	90678
rs764402032	snp	G/T			intron-variant	LRSAM1	GRCh38.p7	9:127480823	CTCCCAAGGAGCTGG[G/T]ACTACAGGCTTGGGC	90678
rs764482781	snp	C/G	1.64743e-05	0.00287	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127473825	TGGAATACTACCCCC[C/G]TTCTCAGTACTTGCT	90678
rs764516956	snp	C/G	1.6892e-05	0.00290615	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127492882	GCAGCGAGAGGAAGA[C/G]CTCCGGGAAATCCTG	90678
rs764633749	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127473174	TCTTGTGACGTGACT[A/G]TATCCTTCCCATGAG	90678
rs764667693	snp	A/G	1.7354e-05	0.00294563	intron-variant	LRSAM1	GRCh38.p7	9:127481252	CTTCCAGGGGAGGGC[A/G]GCATTTTTTTTTTTT	90678
rs764759436	in-del	-/GGA			intron-variant	LRSAM1	GRCh38.p7	9:127479704	CACTGTAGCCTACTG[-/GGA]GGAGCTGGCCGGAGG	90678
rs764802320	snp	A/G	1.65241e-05	0.00287433	missense, intron-variant, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127495332	CAGACGGAGTTAGAA[A/G]CCAAAAGTGAAACCA	90678
rs764809777	snp	C/T	1.64727e-05	0.00286986	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127455040	CTCGACATCTCTAAA[C/T]GTGAGCTCTCAGAGG	90678
rs764852443	in-del	-/C	1.77543e-05	0.0029794	intron-variant	LRSAM1	GRCh38.p7	9:127479542	TCCAGCCTGGCTGCA[-/C]TCCCCCAGCCAGTGG	90678
rs764877541	snp	A/G	3.29832e-05	0.00406085	intron-variant	LRSAM1	GRCh38.p7	9:127473936	TAGAGTGGCAGGTAA[A/G]ACAAGGCAGCCTGCT	90678
rs764878406	snp	A/C			intron-variant	LRSAM1	GRCh38.p7	9:127476314	GGGCTAGTCTATTTC[A/C]ATTCTTATGTTTAAA	90678
rs764890552	snp	A/G	2.98619e-05	0.00386394	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127502880	TCGCCCAGCGCCTCC[A/G]CATCTACCACAGCAG	90678
rs764897663	snp	C/T	1.8449e-05	0.00303713	intron-variant	LRSAM1	GRCh38.p7	9:127454628	GGTTTCCTCTAACTC[C/T]ATCCCATCTCCTCCT	90678
rs764955776	snp	C/T			intron-variant, utr-variant-5-prime	LRSAM1	GRCh38.p7	9:127453760	CACCTCATCCTGCTG[C/T]TCAATGTTTAGTCAA	90678
rs764965750	snp	C/T	1.65444e-05	0.00287609	intron-variant	LRSAM1	GRCh38.p7	9:127485721	CTCAGCTGTCCCCAC[C/T]TCATGTTCCCACAGC	90678
rs765006164	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127489982	CCACGGTGGTCCTGA[C/T]GCCTGCTGAAAAGTG	90678
rs765030169	snp	C/T	1.78618e-05	0.00298841	intron-variant	LRSAM1	GRCh38.p7	9:127492928	CTGTGCTCAGCATCA[C/T]ACAGGCATTTGCTTT	90678
rs765061936	snp	A/T	1.64762e-05	0.00287016	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127462322	CCTCAACATCAGTGG[A/T]AACGAGATCCAGAGA	90678
rs765129368	in-del	-/CC			intron-variant	LRSAM1	GRCh38.p7	9:127488905	AGCTCTTTCCTGCAG[-/CC]CCGTGGGAGTCTTGC	90678
rs765180364	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127501463	TTGGCCAGGCATGGT[A/G]GCTCACGCCTGTAAT	90678
rs765187770	snp	A/G	1.91845e-05	0.00309707	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127502818	CGTCTGCTGCTGCCA[A/G]CAGTGCTGCCAGCCA	90678
rs765202911	in-del	-/AAA			intron-variant	LRSAM1	GRCh38.p7	9:127456163	TAAATGAGAATATGC[-/AAA]AAAAAAAAAAAAAAA	90678
rs765226810	snp	C/T	2.66941e-05	0.00365326	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127489451	TGTTGCAGAGCGCGA[C/T]GCAGAAGGCTGCGTT	90678
rs765301072	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127480741	CACTGAGGCTGGAGT[A/G]CAGTGGTGTGCTCTC	90678
rs765326804	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127461132	GTGCTGGGATTACAG[A/G]CATAAGCCACTGCGC	90678
rs765368812	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127498131	GAGCCAAGGAAGAAG[C/T]GGAGGAGCTGAGGCG	90678
rs765389102	snp	A/C/G/T	0.000131792	0.00811683	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127473824	CTGGAATACTACCCC[A/C/G/T]CTTCTCAGTACTTGC	90678
rs765463549	snp	A/G	1.67598e-05	0.00289476	intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127449721	AGACTAGAAATAAAG[A/G]CATGTAATCAACATG	90678
rs765477712	snp	A/G	8.74317e-05	0.00661122	intron-variant	LRSAM1	GRCh38.p7	9:127467871	CCTCATTGAGGAACT[A/G]TGACCCCCATGGCCA	90678
rs765516153	in-del	-/GA	1.657e-05	0.00287832	intron-variant	LRSAM1	GRCh38.p7	9:127491180	AACTGTGGTTAATGT[-/GA]GTAAAAAAAAACCCT	90678
rs765529227	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127493013	CATCAAAGAAAAACT[A/G]GAAAGTACAAAGGAA	90678
rs765537196	snp	A/G/T	1.65031e-05	0.00287251	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127459003	GTCTTTCTTCTGCAG[A/G/T]TTCTAGATCTCCACG	90678
rs765635982	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127485080	CCCAAAGTGCTGGGA[C/T]TACAGGCATAAGCCA	90678
rs765641195	snp	C/G	0.000333244	0.0129039	splice-donor-variant	LRSAM1	GRCh38.p7	9:127481228	GCTGGAAAATGAAAG[C/G]TAAGTGTTCTTCCAG	90678
rs765667863	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127487399	GCAGGCATCCACTTC[C/T]GGGGGGTGCTGGGGA	90678
rs765677256	snp	A/G	1.68247e-05	0.00290035	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127501134	GTGTGTCGTGTGCCT[A/G]GAACGGGAGGTAAGT	90678
rs765686374	snp	A/C/T	0.000271735	0.011653	intron-variant	LRSAM1	GRCh38.p7	9:127457403	ATCAAGGTACTGGGC[A/C/T]CTCCTCCCAGGCAGC	90678
rs765716709	snp	C/T	1.65905e-05	0.0028801	intron-variant	LRSAM1	GRCh38.p7	9:127480030	TTCCCCGTGCAGTCC[C/T]CTGAGGAGCCGGGAG	90678
rs765772808	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127457992	TTTTTTAATATTTTG[C/T]ACCTGAGTTTGGTTG	90678
rs765780655	snp	C/G	1.74057e-05	0.00295001	utr-variant-5-prime, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451361	CGGATTCGGGACGAC[C/G]GAAGGAAGTTGCACC	90678
rs765806160	in-del	-/C			intron-variant	LRSAM1	GRCh38.p7	9:127454751	ACCCAACAGATGAGG[-/C]CCCCCTGCCAAGGGT	90678
rs765887713	in-del	-/C			intron-variant	LRSAM1	GRCh38.p7	9:127495164	TCCATGTTGGTCAGG[-/C]CTGGTCTTGAACTCC	90678
rs765893788	snp	C/T	1.67181e-05	0.00289115	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127454537	GGAAGGATGCCGCTC[C/T]TCTTCCGGAAGCGGA	90678
rs765928752	snp	A/T			missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127487723	TTCTGTCGTGGCAGC[A/T]AATGGATCAGAACAA	90678
rs765956865	snp	A/C	0.000355961	0.0133362	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127502789	GCCCAGATGATCTTC[A/C]TCAACTGTGGCCACG	90678
rs765969094	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127487962	ATGGTCTTCTGGTCA[C/T]TAAAATCCACAGAAG	90678
rs765985792	snp	C/T	0.00010721	0.00732075	intron-variant	LRSAM1	GRCh38.p7	9:127454615	GTGAGGGAAAGTGGG[C/T]TTCCTCTAACTCTAT	90678
rs766032321	snp	A/G	1.65509e-05	0.00287666	synonymous-codon, intron-variant, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127495322	TCATTCCTGGCAGAC[A/G]GAGTTAGAAGCCAAA	90678
rs766054234	snp	C/G	1.65214e-05	0.0028741	intron-variant	LRSAM1	GRCh38.p7	9:127461292	GTCCGTGTGACCCTC[C/G]ATCAGCTCTGGGCCA	90678
rs766076120	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127466981	CAGTCTGGGCAATGG[A/G]AATGAGACCCTGTCT	90678
rs766114300	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127461309	TCAGCTCTGGGCCAT[C/T]CTGGCCGGGATCCAC	90678
rs766122528	snp	A/G	1.71584e-05	0.00292898	intron-variant	LRSAM1	GRCh38.p7	9:127492904	GAAATCCTGGTATGT[A/G]TTTGGCTTCTGTGCT	90678
rs766123152	in-del	-/AA/AAA			intron-variant	LRSAM1	GRCh38.p7	9:127499055	GTGAAACTCTGTCTC[-/AA/AAA]AAAAAAAAAAAAGAA	90678
rs766153071	snp	C/T	1.65381e-05	0.00287555	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127501019	CCACAGAGCTGAAAC[C/T]ACCAATGGGTGAGGT	90678
rs766174549	snp	A/C			intron-variant	LRSAM1	GRCh38.p7	9:127463545	TCATCTTCCCTGTGT[A/C]CATGTCCGGGTCCAA	90678
rs766200273	snp	A/T	3.2956e-05	0.00405918	intron-variant	LRSAM1	GRCh38.p7	9:127479539	AGGGTCCAGCCTGGC[A/T]GCATCCCCCAGCCAG	90678
rs766238950	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127480464	GTCTAGTGAGGGGGC[C/G]CATTGCAGGATGATT	90678
rs766240019	snp	C/T	3.4954e-05	0.00418041	intron-variant	LRSAM1	GRCh38.p7	9:127501158	GGTAAGTCCGGGGCC[C/T]TCCCCACCCGCCTGC	90678
rs766244006	snp	G/T			intron-variant	LRSAM1	GRCh38.p7	9:127498928	GCCAGGCGTGGTGGC[G/T]TGCACCTGTAGTCCC	90678
rs766288153	snp	C/T	1.65089e-05	0.00287301	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127479437	CTGGAACTGGGGCAG[C/T]GGGAGCACACCCAGC	90678
rs766297623	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127465568	GCCCTCAGCATCTGG[C/G]CGGTCAGTTCCTCTT	90678
rs766326390	snp	C/T	6.15795e-05	0.00554851	intron-variant	LRSAM1	GRCh38.p7	9:127487783	GCCCTCGCCCAGAGC[C/T]TGAGGGTGGGAGCTC	90678
rs766431704	snp	A/G	3.46284e-05	0.00416089	intron-variant	LRSAM1	GRCh38.p7	9:127467860	CTGCCTCCTCCCCTC[A/G]TTGAGGAACTATGAC	90678
rs766441345	snp	C/T	4.09232e-05	0.00452327	intron-variant	LRSAM1	GRCh38.p7	9:127492762	GGACTCCTGCGCTGC[C/T]GCCAGCTCACGGTGG	90678
rs766476460	snp	C/G	0.000164718	0.00907368	intron-variant	LRSAM1	GRCh38.p7	9:127455074	ACTGAGGATAGTGTT[C/G]GGCTGTGAATTGGAT	90678
rs766651362	snp	A/C	1.65559e-05	0.00287709	intron-variant	LRSAM1	GRCh38.p7	9:127480025	AGTCCTTCCCCGTGC[A/C]GTCCCCTGAGGAGCC	90678
rs766700610	in-del	-/GGTGAGGGAAAGTGGGTTTCCTC	1.71252e-05	0.00292614	frameshift-variant, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127454598	GTACCAGATGTGTTT[-/GGTGAGGGAAAGTGGGTTTCCTC]GGTGAGGGAAAGTGG	90678
rs766701971	snp	C/T	3.30186e-05	0.00406303	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127479970	GAAGCTGCTGCAGGA[C/T]AATCAGAGGTTGGGC	90678
rs766732934	snp	A/C/G	5.19902e-05	0.00509832	utr-variant-5-prime, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451355	TGAACCCGGATTCGG[A/C/G]ACGACCGAAGGAAGT	90678
rs766738884	snp	A/C			intron-variant	LRSAM1	GRCh38.p7	9:127484061	CAACTGAAACTGTCC[A/C]TAGTAAACACTAACT	90678
rs766742774	snp	A/G	1.65814e-05	0.00287931	intron-variant	LRSAM1	GRCh38.p7	9:127459092	GCTGCAGAAACAGAA[A/G]CCCACCTCGGATGGC	90678
rs766760217	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127471299	GCAACATGGCAAAAC[C/T]TCATCTCTACAAAAA	90678
rs766761756	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127485899	TCAGGGCCCAAGACC[A/G]TGGGATGAGAGCTGG	90678
rs766778915	snp	C/T	1.74925e-05	0.00295735	intron-variant	LRSAM1	GRCh38.p7	9:127491329	CCCTGCCCTCCTTCA[C/T]GTGGTGAGACCCCCA	90678
rs766784003	in-del	-/AT			intron-variant	LRSAM1	GRCh38.p7	9:127486603	CTCCCCCCTTTCCTG[-/AT]ATGTGACACTGTGCT	90678
rs766819671	in-del	-/T	1.64749e-05	0.00287005	intron-variant	LRSAM1	GRCh38.p7	9:127478895	AGGGAGAACCACTGC[-/T]GCCACCCTCTCTTGA	90678
rs766862972	snp	A/G	1.66021e-05	0.0028811	intron-variant	LRSAM1	GRCh38.p7	9:127489567	CTCTCAGAGACTTGC[A/G]GAGTGGCCCTCCAGG	90678
rs766865080	snp	A/G	4.95892e-05	0.00497917	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127501048	GTCGTCACCCCTACG[A/G]CCCCCCAGGAGCCTC	90678
rs766883080	snp	G/T	0.000120031	0.00774602	intron-variant	LRSAM1	GRCh38.p7	9:127497386	CCAGCCGTATGTGTG[G/T]GCTCTGGTGGGGACA	90678
rs766904787	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127482758	TCTTTTTACACAAGA[C/T]ACTCGAACTACAGGC	90678
rs767011373	snp	A/G	1.64741e-05	0.00286998	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127461218	CAGCTCCCACGTTCC[A/G]TTGGGAACCTGACCC	90678
rs767095874	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127486181	GTTCTGAGAAACTGT[A/G]TAACGCACCCAAGGA	90678
rs767107676	snp	C/G	1.65012e-05	0.00287234	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127479425	TTTGAACGGCGCCTG[C/G]AACTGGGGCAGCGGG	90678
rs767137099	snp	C/T			upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	RPL12, LRSAM1	GRCh38.p7	9:127451559	AGCAGGGCACCGCGG[C/T]GCGCTGAAGCTAGAG	90678
rs767139754	snp	A/G	1.70145e-05	0.00291667	intron-variant	LRSAM1	GRCh38.p7	9:127479532	GCCTGCTAGGGTCCA[A/G]CCTGGCTGCATCCCC	90678
rs767192481	snp	A/C/G/T	0.000139507	0.00835091	utr-variant-5-prime, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451365	TTCGGGACGACCGAA[A/C/G/T]GAAGTTGCACCTTGG	90678
rs767202684	in-del	-/CCTGGT	0.000104031	0.00721143	utr-variant-3-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127502919	GCCCGCCCACCTGGG[-/CCTGGT]CCTGGTCCTAGCCCT	90678
rs767232209	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127496166	CAGCCGGGGGTTGAT[C/T]TGCTCCTTGTGTAGT	90678
rs767249563	snp	A/G	0.000102129	0.00714523	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127501143	GTGCCTGGAACGGGA[A/G]GTAAGTCCGGGGCCC	90678
rs767289616	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127492703	GCATTGGGCAGAGAA[C/T]CGAGTGAGCGGGAGG	90678
rs767307606	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127494076	GCGCTGTGCCTTAGC[A/G]GCCAGGTACTATGGC	90678
rs767315094	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127465446	GTAGCCAGCATCCTG[A/G]TATAGCCCACAGTCC	90678
rs767346137	in-del	-/T			intron-variant	LRSAM1	GRCh38.p7	9:127469173	AGACTTGACTAAGAA[-/T]TTTTACACAAGAGAA	90678
rs767351229	snp	A/G	7.24283e-05	0.00601739	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127487683	TCTGGCAGCATGGCC[A/G]AAATGGATGAACGAT	90678
rs767397160	snp	A/G	1.64955e-05	0.00287184	intron-variant	LRSAM1	GRCh38.p7	9:127479343	TGTCCTAACTCCCCC[A/G]GGGCCTGTGCTGACA	90678
rs767406880	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127463936	AGGCAGTTTAAGAAA[C/T]TTGCCCAAGGGCCAC	90678
rs767413847	snp	A/C/T	6.99232e-05	0.00591248	intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127449574	TGCTACCTGTCCCCC[A/C/T]ACCCTCCTCTCCCGA	90678
rs767417984	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127478152	AAACACCAATAATTA[C/T]ATTACATTATTGATG	90678
rs767439257	snp	A/G	1.65239e-05	0.00287431	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127485825	AACTTGGTCCAGCAG[A/G]CCTGTTCCAGGTAAG	90678
rs767459848	snp	A/G	3.47554e-05	0.00416851	intron-variant	LRSAM1	GRCh38.p7	9:127495949	CTGCTCATGGTACAC[A/G]TTTCTGTCTTGCAGG	90678
rs767506004	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127455239	TGGCCTCAATATAAC[A/G]TAGTCTCCAAGAGTC	90678
rs767532563	snp	A/C/G	4.96515e-05	0.00498234	intron-variant	LRSAM1	GRCh38.p7	9:127480021	CCAGAGTCCTTCCCC[A/C/G]TGCAGTCCCCTGAGG	90678
rs767554565	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127456666	TCAGGAGATCAAGAC[C/T]ATCCTGGCTACCATG	90678
rs767576596	in-del	-/CT	1.65743e-05	0.00287869	intron-variant	LRSAM1	GRCh38.p7	9:127491195	GAGTAAAAAAAAACC[-/CT]GTCTCGTCTTCTGTT	90678
rs767583106	snp	C/T	0.000277136	0.0117682	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127467779	ATGGTCTACCCGCCG[C/T]GGGAGGTGTGTGGTG	90678
rs767645690	snp	A/G			downstream-variant-500B	LRSAM1	GRCh38.p7	9:127503744	ATGGCTGCGGCCTGT[A/G]CCTCCATGAGCGGAG	90678
rs767680661	snp	A/G	1.70557e-05	0.0029202	missense, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451310	TTGGGGTCGAACTTC[A/G]GCGGCATGGTGGAGG	90678
rs767728855	snp	C/T	2.4446e-05	0.00349605	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127489472	AGGCTGCGTTCGAGG[C/T]ACTCCAGGTGAAGAA	90678
rs767746171	snp	A/G	3.36649e-05	0.0041026	intron-variant	LRSAM1	GRCh38.p7	9:127467707	GGTTGCGTTGGTAGC[A/G]AACAGTAAAGCGGGT	90678
rs767773449	snp	C/T			upstream-variant-2KB, intron-variant	RPL12, LRSAM1	GRCh38.p7	9:127453170	CACTGCAACCTCTGC[C/T]TCCTGGGTTCAAGCA	90678
rs767787667	snp	C/T	3.58327e-05	0.00423262	intron-variant	LRSAM1	GRCh38.p7	9:127489546	GCTGGGGTCCCTGGA[C/T]CTGCTCTCTCAGAGA	90678
rs767826471	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127469198	AGAGAATATCCACAC[A/G]GTGGCTCACACCTGT	90678
rs767830115	snp	A/G	1.6507e-05	0.00287284	intron-variant	LRSAM1	GRCh38.p7	9:127458987	TTGGAGACTCACAGG[A/G]GTCTTTCTTCTGCAG	90678
rs767838251	snp	A/G	3.29848e-05	0.00406095	intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451235	ACGCGCGGCAGGGCC[A/G]AGGGATGCTCCATCC	90678
rs767878162	snp	C/T	3.4009e-05	0.00412351	intron-variant	LRSAM1	GRCh38.p7	9:127497376	AGGCAGGGCTCCAGC[C/T]GTATGTGTGGGCTCT	90678
rs767888911	in-del	-/G	1.74221e-05	0.00295139	utr-variant-5-prime, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451365	TTCGGGACGACCGAA[-/G]GAAGTTGCACCTTGG	90678
rs767900300	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127483723	GGCTGGAGTACAGTG[C/G]TGCGATCTTGGCTCA	90678
rs767906767	in-del	-/AAAG			intron-variant	LRSAM1	GRCh38.p7	9:127476552	AGACCCTATCTCAAA[-/AAAG]AAAGAAAAAGAAAAC	90678
rs767930199	snp	G/T			intron-variant	LRSAM1	GRCh38.p7	9:127502329	GCCGTGCCTGTTCTG[G/T]TTCTGTGGTGGTCAA	90678
rs767975258	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127461871	TGTTTATCAACTGTA[A/G]CATATGAGTAATGAG	90678
rs767986007	snp	A/C			intron-variant	LRSAM1	GRCh38.p7	9:127482925	ATGTTAAATTTGCTG[A/C]ATGAATGGATGGATT	90678
rs767987410	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127476458	GAGGCTAAGGTGGGA[A/G]GATGGCTTAAGCCCA	90678
rs768049093	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127460646	GTGCTCTCCTGAGCA[C/T]GTGACTTTGCCACCC	90678
rs768056477	snp	A/C	1.65452e-05	0.00287616	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127457331	GTGCTGATCGTCCAC[A/C]CGAATCACCTCACTT	90678
rs768060451	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127497568	TCCACGTAGCAGTGG[A/G]GGGGCCCTCCCAGCT	90678
rs768076141	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127495247	CATGAGCCACCGCGC[C/T]TGGCAACCATCATTG	90678
rs768142711	snp	A/G	1.70026e-05	0.00291565	intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127450693	CGCTTAAAGTGAAAC[A/G]AATGTGAAAAAAATG	90678
rs768150732	snp	A/C			intron-variant	LRSAM1	GRCh38.p7	9:127493350	TACAGGCATGAGCCA[A/C]CGCGCCTAGCCTCTC	90678
rs768288133	snp	A/G	5.13466e-05	0.00506662	intron-variant	LRSAM1	GRCh38.p7	9:127496109	AGGTGGGCAGCAGCC[A/G]TCTGCATGGAGGGGA	90678
rs768290843	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127480083	CTCTGCCCCTGCCCC[A/G]GGCTTCCCTTGTCAG	90678
rs768302528	snp	A/G	3.40084e-05	0.00412347	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127496022	TGTCGGCTGAGCACT[A/G]CCTGCCCATCTTTGC	90678
rs768307214	snp	A/T	4.94858e-05	0.00497398	intron-variant	LRSAM1	GRCh38.p7	9:127455659	AGACTTTCTTGTTGC[A/T]TGTCTGCTTGTTTGA	90678
rs768346182	snp	C/T	1.98458e-05	0.00315	intron-variant, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127487662	AATGAATGAATTTGC[C/T]GTCTTTCTGGCAGCA	90678
rs768355188	snp	A/G			upstream-variant-2KB, intron-variant	RPL12, LRSAM1	GRCh38.p7	9:127452580	TGTGGGTTGCTTTGT[A/G]GCTAACATTTATTGA	90678
rs768380430	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127479153	ATCCATGGGACAGGT[A/G]CAGAGACTGAGGCTC	90678
rs768438916	snp	C/G	1.72633e-05	0.00293791	utr-variant-5-prime, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451346	GGTGTCGGATGAACC[C/G]GGATTCGGGACGACC	90678
rs768441331	snp	G/T			intron-variant	LRSAM1	GRCh38.p7	9:127456235	TGGAAGTTTTGTTTG[G/T]TTTTTTTTTTTTTTG	90678
rs768499549	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127472392	CACACCTATAATCCC[A/G]TAACTTTGGGAGACC	90678
rs768512420	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127485604	TTTTTTTTAAGATAA[C/T]TATCAGGTAGGTAAC	90678
rs768537136	snp	C/T	1.64988e-05	0.00287213	synonymous-codon, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127449643	AATGGTCAGTTTCAC[C/T]GTAATCCTCAGGCCC	90678
rs768625749	snp	C/T			missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127495986	GGATGGAGCGCCAGC[C/T]GGTGGCCCTCCTGGA	90678
rs768658255	snp	C/T	4.96438e-05	0.00498191	intron-variant	LRSAM1	GRCh38.p7	9:127480019	CCCCAGAGTCCTTCC[C/T]CGTGCAGTCCCCTGA	90678
rs768701463	snp	C/G/T	3.30067e-05	0.00406232	intron-variant	LRSAM1	GRCh38.p7	9:127461139	GATTACAGGCATAAG[C/G/T]CACTGCGCCTGGCTG	90678
rs768759548	snp	A/C/T	3.39595e-05	0.00412053	intron-variant	LRSAM1	GRCh38.p7	9:127497372	TTCCAGGCAGGGCTC[A/C/T]AGCCGTATGTGTGGG	90678
rs768761191	snp	A/G	5.11043e-05	0.00505465	synonymous-codon, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451303	GATCTCGTTGGGGTC[A/G]AACTTCGGCGGCATG	90678
rs768791464	snp	C/T	1.65127e-05	0.00287334	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127459040	AGCTGACAGCCCTTC[C/T]TGACGATCTGGGGCA	90678
rs768799611	snp	A/T	3.34107e-05	0.00408708	intron-variant	LRSAM1	GRCh38.p7	9:127473982	TGTGTGTGCGTGTGC[A/T]TGTATGTGTGTTGAG	90678
rs768889482	snp	G/T	6.59011e-05	0.00573988	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127473908	CCCACGGACAGATTC[G/T]CAAGGGAGGAGTTAG	90678
rs768898199	snp	A/C			intron-variant	LRSAM1	GRCh38.p7	9:127462710	AGAGCATCAGGAAGA[A/C]AAGCTAATGGATGCT	90678
rs768901152	in-del	-/ATATATATA			intron-variant	LRSAM1	GRCh38.p7	9:127466495	TATATATATATATAT[-/ATATATATA]ATATATATATTTTTT	90678
rs768911902	in-del	-/C			intron-variant	LRSAM1	GRCh38.p7	9:127493170	GGCTCAAGCGATCCT[-/C]CCCACCTCAGCTTCC	90678
rs768915191	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127490587	CCCAGAGAAAGGGAT[C/G]TCTCCCTTACCTGCT	90678
rs768968569	in-del	-/TAAGACAAGGCAGCC	1.64867e-05	0.00287107	splice-donor-variant	LRSAM1	GRCh38.p7	9:127473933	AGTTAGAGTGGCAGG[-/TAAGACAAGGCAGCC]TGCTGCACGCATACA	90678
rs769013853	in-del	-/TTTC			intron-variant	LRSAM1	GRCh38.p7	9:127490250	CTTTCTCTATTTTTC[-/TTTC]TTTCTTTCTTTCTTT	90678
rs769020006	in-del	-/A	0.000427223	0.0146092	intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127450699	AGTGAAACAAATGTG[-/A]AAAAAAATGCCCCTT	90678
rs769070078	snp	A/C	1.64727e-05	0.00286986	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127455014	CAAAAGAAGCTGGGG[A/C]AGATGACATTCTCGA	90678
rs769110240	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127489772	GCGGGTCTCCACCAC[A/G]CCTGGGCCAGGGAGG	90678
rs769164021	snp	A/G	0.000214145	0.0103454	intron-variant	LRSAM1	GRCh38.p7	9:127462385	GGAGGTAAATGGGAA[A/G]CTGTTCTTGCCTGGG	90678
rs769178539	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127477541	GATGCTTGAGCTCAG[C/G]AGTTTGAGACCATCC	90678
rs769196517	snp	C/T	5.02938e-05	0.00501442	intron-variant	LRSAM1	GRCh38.p7	9:127495301	TTGTGACTAACATTG[C/T]CTGCTTCATTCCTGG	90678
rs769228833	in-del	-/AAAT			intron-variant	LRSAM1	GRCh38.p7	9:127472643	AGACTCCATCTCAAA[-/AAAT]AAATAAATAAATAAA	90678
rs769236666	snp	A/T	1.69703e-05	0.00291288	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127454591	CGCCTGGAGTACCAG[A/T]TGTGTTTGGTGAGGG	90678
rs769238014	snp	C/T	1.70528e-05	0.00291995	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127496010	TCCTGGAGGAGCTGT[C/T]GGCTGAGCACTACCT	90678
rs769269709	snp	C/G/T	6.59939e-05	0.00574397	intron-variant	LRSAM1	GRCh38.p7	9:127455657	AGAGACTTTCTTGTT[C/G/T]CATGTCTGCTTGTTT	90678
rs769273444	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127492475	CCCACACTGCTCCCC[A/G]CCATTTGCTTCTGCC	90678
rs769296438	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127493269	GTTTCGCTATGTTGC[C/T]CAGGCTGGTCTCCAA	90678
rs769334619	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127466555	ATGGGGTCTCGCTAT[A/G]TTGCCCAGGCTGGTC	90678
rs769340725	snp	C/T			upstream-variant-2KB, intron-variant	RPL12, LRSAM1	GRCh38.p7	9:127453324	TGGGCTCAAGTGACC[C/T]ACCTGTCTTGGCCTC	90678
rs769357543	snp	A/G	3.29495e-05	0.00405877	intron-variant	LRSAM1	GRCh38.p7	9:127455543	AAAAACTGGCAGGAG[A/G]GGAGACACTTACTCT	90678
rs769419126	snp	G/T			intron-variant	LRSAM1	GRCh38.p7	9:127495841	TACCTATGAGTTTTT[G/T]TAGGAAAAATCCCGA	90678
rs769420202	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127492383	GTTGGGGCCCCCATG[A/G]GGTTTCCAAGAGCAG	90678
rs769461961	snp	C/T	3.29516e-05	0.00405891	intron-variant	LRSAM1	GRCh38.p7	9:127462418	GCTCTCTGGCCTGCC[C/T]ACCTCCCCTCTCTCC	90678
rs769472497	snp	C/T	1.75533e-05	0.00296249	intron-variant	LRSAM1	GRCh38.p7	9:127495930	TGGGTTCTTTTCTTC[C/T]TTCCTGCTCATGGTA	90678
rs769479121	snp	A/G	1.69963e-05	0.00291511	missense, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451289	CACGCACCGACTTTG[A/G]TCTCGTTGGGGTCGA	90678
rs769490948	snp	G/T	8.54591e-05	0.00653623	utr-variant-3-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127502951	CCTCGGCCACTGTGA[G/T]CCCCGGGCTCCTGCT	90678
rs769500816	snp	A/C			intron-variant	LRSAM1	GRCh38.p7	9:127470607	GTCCAACCTGGAAAC[A/C]GCTTTAATGTCCATT	90678
rs769513187	snp	C/T	4.957e-05	0.00497821	intron-variant	LRSAM1	GRCh38.p7	9:127479995	TTGGGCTCTGCTCCT[C/T]GGCCCCAGCCCCAGA	90678
rs769537839	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127470637	TAGGAGTAGAATGGA[C/T]AACTAAACTGTTTTA	90678
rs769569457	snp	A/G	1.65031e-05	0.00287251	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127459025	ATCTCCACGATAATC[A/G]GCTGACAGCCCTTCC	90678
rs769581855	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127483434	CCTGGGTAATACAGC[A/G]AGACCATTTCTCAGA	90678
rs769751278	snp	A/G	3.32132e-05	0.00407499	missense, intron-variant, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127491257	CAGCTGACACAGCTG[A/G]AGTTAAAGAGGAAGT	90678
rs769821359	in-del	-/T			intron-variant	LRSAM1	GRCh38.p7	9:127482142	ATTTTTAGTATATCT[-/T]TTTTTTTTTTTTTTT	90678
rs769842908	snp	A/G	2.65798e-05	0.00364544	intron-variant	LRSAM1	GRCh38.p7	9:127489525	AGGAGCCAGGTGAGC[A/G]CTGGGGCTGGGGTCC	90678
rs769859385	snp	C/T	0.00213169	0.0325776	intron-variant	LRSAM1	GRCh38.p7	9:127497370	TCTTCCAGGCAGGGC[C/T]CCAGCCGTATGTGTG	90678
rs769884345	snp	A/C	4.95487e-05	0.00497714	intron-variant	LRSAM1	GRCh38.p7	9:127458967	AGTCTGAGGGACTTT[A/C]TCACTTGGAGACTCA	90678
rs769930277	snp	A/G	3.295e-05	0.00405881	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127473898	CCCTGATGGGCCCAC[A/G]GACAGATTCTCAAGG	90678
rs769946237	snp	C/G	1.65905e-05	0.0028801	intron-variant	LRSAM1	GRCh38.p7	9:127485686	CTCCCTGCCCAGGTG[C/G]CCCAGGAGCAGCCAC	90678
rs770006810	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127475632	ATGACAATTTCTGTT[A/G]GCCAGAGTATGGGAA	90678
rs770038352	snp	A/G	6.9006e-05	0.00587352	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127482985	TGTCCATAACCCAGG[A/G]GGAGACTGAGAGCCT	90678
rs770082381	snp	A/G			upstream-variant-2KB, intron-variant	RPL12, LRSAM1	GRCh38.p7	9:127453135	CACCCAGGCTGGAGT[A/G]CAGTGGCATGATCTT	90678
rs770106776	snp	A/G	6.77805e-05	0.00582114	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127502856	CCTGCCCGCTGTGCC[A/G]CCAGGACATCGCCCA	90678
rs770244104	snp	A/G	1.68391e-05	0.0029016	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127492872	AAGAGAAGCAGCAGC[A/G]AGAGGAAGAGCTCCG	90678
rs770257786	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127460374	ACCACCTTCTGGAGG[C/G]AGCACAGCTTCGGAA	90678
rs770259167	snp	C/T	5.04037e-05	0.00501989	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127454576	GAGGAGGCTCGGAAA[C/T]GCCTGGAGTACCAGA	90678
rs770265832	in-del	-/C	4.96528e-05	0.00498236	intron-variant	LRSAM1	GRCh38.p7	9:127501001	GTCTGTCTGTCTGGT[-/C]CCCCACAGAGCTGAA	90678
rs770311376	snp	C/G			utr-variant-5-prime, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451393	TGGCCTCCTCCGAGC[C/G]GAAAGCCGAGAGGCC	90678
rs770331997	snp	A/G	8.97239e-05	0.00669731	intron-variant	LRSAM1	GRCh38.p7	9:127502736	GGACTCCTGGAACCC[A/G]GTAGGGCCAGCCACA	90678
rs770333450	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127489914	TCAGACAGACAGAGG[C/T]GTCTCAGGGGCATAT	90678
rs770348926	snp	C/G	1.64819e-05	0.00287066	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127462283	GCTTCCAGACACCGT[C/G]GGGGAGCTTCGAAGC	90678
rs770365427	snp	A/G	6.60066e-05	0.00574447	intron-variant	LRSAM1	GRCh38.p7	9:127461275	AGGGACCAAGAAGCC[A/G]TGTCCGTGTGACCCT	90678
rs770394681	snp	C/T	1.70478e-05	0.00291952	utr-variant-3-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127502946	CCCTGCCTCGGCCAC[C/T]GTGAGCCCCGGGCTC	90678
rs770398029	snp	A/G	5.75192e-05	0.00536249	intron-variant	LRSAM1	GRCh38.p7	9:127467844	AGGTAAAGCCAGGCC[A/G]CTGCCTCCTCCCCTC	90678
rs770410548	snp	C/T	2.4317e-05	0.00348682	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127467754	GATGCTGAGCCTTGA[C/T]GCCTCGGCCATGGTC	90678
rs770441992	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127469712	CTCGCGCCTGTAATC[C/T]CAGCACTTTGGGAGG	90678
rs770471321	in-del	-/C			intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127450192	ACCAATGGGGAAGAG[-/C]ATTTGGGGCAGGGGA	90678
rs770562865	snp	A/G			upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	RPL12, LRSAM1	GRCh38.p7	9:127451988	TGCCGGGTGGTCTGC[A/G]GCCCCGAGTCCGTGA	90678
rs770571067	snp	C/G			intron-variant, utr-variant-5-prime	LRSAM1	GRCh38.p7	9:127453598	TCATTGGCAGAGTCT[C/G]TTAGAGTCCTCAAAG	90678
rs770590486	snp	A/G	5.0413e-05	0.00502035	intron-variant	LRSAM1	GRCh38.p7	9:127479831	AGGACCCCTACCTCC[A/G]GCTGCAGGAGCAGTC	90678
rs770610024	snp	A/G	0.000111951	0.00748083	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127502874	AGGACATCGCCCAGC[A/G]CCTCCGCATCTACCA	90678
rs770641135	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127502270	ACAAACTATAGAGAA[A/G]TAGACAGCAAACTGC	90678
rs770661016	snp	A/T			intron-variant	LRSAM1	GRCh38.p7	9:127468334	GAGGAGGAAAGAAAG[A/T]GTGCAGGACAGGGGA	90678
rs770663771	snp	C/G/T	0.000170533	0.00923253	intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451268	CAGCCCCGGCCACAA[C/G/T]CAGAGCACGCACCGA	90678
rs770667136	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127492792	GTGCGGGGTGTGGTC[C/T]TGTTCGCAGGAGATG	90678
rs770711645	snp	A/G	1.64741e-05	0.00286998	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127473888	CTCGGGACAGCCCTG[A/G]TGGGCCCACGGACAG	90678
rs770758847	snp	G/T	1.65921e-05	0.00288024	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127497271	GGCGTCTCAGAAGCT[G/T]GCCTGCAGCACGAGA	90678
rs770785162	in-del	-/TT	1.64819e-05	0.00287066	intron-variant	LRSAM1	GRCh38.p7	9:127461165	GGCTGCCTCTTCCTC[-/TT]TCTTAGGTCTTAAAC	90678
rs770789095	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127494560	TACGCCTGTTGTCAC[C/T]GTGGCTGTTATCAGC	90678
rs770799976	snp	C/T	1.70974e-05	0.00292376	intron-variant	LRSAM1	GRCh38.p7	9:127497360	AGCTCCAGCCTCTTC[C/T]AGGCAGGGCTCCAGC	90678
rs770822771	in-del	-/GTCC	6.77369e-05	0.00581927	intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127449738	TGTAATCAACATGGT[-/GTCC]GTCCAGAGGTGAACC	90678
rs770853713	in-del	-/AGA			intron-variant	LRSAM1	GRCh38.p7	9:127500841	TGAGGCTCAGAGAAG[-/AGA]AGAAGAGAGTGTGTG	90678
rs770858874	in-del	-/CCA			intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127449771	AGCCTTGAAACCTGC[-/CCA]CCACTTCTCACTTGG	90678
rs770878674	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127493868	CGTTCCTGTGTCCCC[A/G]TGAATGCACCAGATG	90678
rs770913245	snp	C/G	6.18754e-05	0.00556182	intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127450721	ATGCCCCTTGGAGGG[C/G]ATAACGTACCAGACC	90678
rs770935955	in-del	-/CACAGTCTGCACTTCCTTGAACTGT	1.66701e-05	0.002887	intron-variant	LRSAM1	GRCh38.p7	9:127497223	GGCTCCCGCCCAGGC[-/CACAGTCTGCACTTCCTTGAACTGT]CACAGGTGGGCGTCT	90678
rs770976584	snp	A/G			downstream-variant-500B	LRSAM1	GRCh38.p7	9:127503634	GCACCTCAGTCGAGA[A/G]GAGAGGTCAGGTAGG	90678
rs770988636	in-del	-/CAAA			intron-variant	LRSAM1	GRCh38.p7	9:127475493	AATGAGACTCCATCT[-/CAAA]CAAACAAACAAACAA	90678
rs771006038	snp	A/C/T	5.07636e-05	0.00503778	utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127454508	CAGGGTCCTAAAGAT[A/C/T]GCTCTGGGAAAAGGG	90678
rs771047258	snp	C/T	3.33979e-05	0.0040863	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127454560	GAAGCGGAAACCCAG[C/T]GAGGAGGCTCGGAAA	90678
rs771060344	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127459984	AATGGCTACTTAGCT[C/T]TCCATTGCATCATTT	90678
rs771071984	in-del	-/CC			intron-variant	LRSAM1	GRCh38.p7	9:127486479	GGGACAGGCCAGCAG[-/CC]CTGGATGCCCTGTTT	90678
rs771076859	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127459694	CTCCTGAGTATCTGG[A/G]ATTACAGGCACACGC	90678
rs771081300	snp	G/T	3.36576e-05	0.00410215	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127492851	CCCTGCTCCAGCAGC[G/T]GCTCAAAGAGAAGCA	90678
rs771106613	snp	C/T	1.85806e-05	0.00304794	intron-variant	LRSAM1	GRCh38.p7	9:127482939	GAATGAATGGATGGA[C/T]TTTTTTCTAGAATAA	90678
rs771147504	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127488635	GGTCTTGCTCTGTTG[C/T]CCAGGATGAGTGAAG	90678
rs771242310	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127472802	CCTTAAACTGGTCAC[A/G]GGATTTCATGTGGTG	90678
rs771291501	snp	C/T			intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127450079	GCTACTCTGAAGTTC[C/T]CCTCCTCTAGTAATC	90678
rs771380760	snp	G/T	1.64757e-05	0.00287012	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127461182	TCTTAGGTCTTAAAC[G/T]TGGAAAGGAATCAAC	90678
rs771400112	in-del	-/CA	3.14016e-05	0.0039623	intron-variant	LRSAM1	GRCh38.p7	9:127489422	ACGGCCCCTGCTGAG[-/CA]GGCTGGTGGTCTGTG	90678
rs771415278	snp	C/T	1.84828e-05	0.00303991	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127487745	TCAGAACAAAGCCAT[C/T]AGCCAGATCCTGCAG	90678
rs771421632	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127465054	TGAGTTCAGGCCGTA[C/G]TGTGGGCAAGATCTT	90678
rs771480471	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127500540	CCTGATGGGCAGCAG[C/T]CCATCCTGTCTCCTG	90678
rs771491533	snp	A/G	1.66682e-05	0.00288684	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127479496	TGAGATCCTTCAGAC[A/G]GTCAAGGAGGTTTGT	90678
rs771498810	snp	A/G	0.000107406	0.00732743	intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127450838	TAGTGTCTGTGCAGA[A/G]GGAGCCCCGAGCCAC	90678
rs771510127	snp	C/T	3.29891e-05	0.00406122	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127479406	GATGCTGGAGAAACT[C/T]GAGTTTGAACGGCGC	90678
rs771511537	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127478666	ATCCCTGCTCAGGGC[C/T]GCATCCCAGAACTGT	90678
rs771574214	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127481717	TGAAAAACATTCAGA[A/G]ACATGAATAAGGCTA	90678
rs771599803	snp	A/G	4.45177e-05	0.00471772	intron-variant, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127487639	AGGTGCTCGGGAAAC[A/G]TTCCAAGAATGAATG	90678
rs771653490	snp	A/G	2.79709e-05	0.0037396	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127489445	GGTCTGTGTTGCAGA[A/G]CGCGATGCAGAAGGC	90678
rs771741363	snp	C/T	3.94921e-05	0.00444348	intron-variant	LRSAM1	GRCh38.p7	9:127487770	CTGCAGGAGGTGAGC[C/T]CTCGCCCAGAGCCTG	90678
rs771751705	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127494428	GGTTACTCATCACCC[C/T]GAACCTCAGCTCCCT	90678
rs771783337	snp	A/G	0.000182614	0.00955371	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127497253	CTTGAACTGTCACAG[A/G]TGGGCGTCTCAGAAG	90678
rs771839455	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127493476	CGAGCAGCCTGTTTC[C/T]GCACATTCTTTTCAA	90678
rs771900685	snp	A/G	1.72027e-05	0.00293275	intron-variant	LRSAM1	GRCh38.p7	9:127496123	CGTCTGCATGGAGGG[A/G]AGGGGCACGCAAGGC	90678
rs771907945	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127459651	GCAACATCTGCCTCC[C/T]GGGTTCAAGAGATTC	90678
rs771954471	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127500191	CATGGTGAAACCCCA[C/T]CTCTACTAAAGATAC	90678
rs772043012	snp	A/C			intron-variant	LRSAM1	GRCh38.p7	9:127498200	CGGGGCTCCAGGGGG[A/C]TGGGCTGACTGCAGC	90678
rs772047683	snp	C/T	3.29549e-05	0.00405911	intron-variant	LRSAM1	GRCh38.p7	9:127473789	GGTCAGCTTGTGTCC[C/T]GTCTCTTACAGAGTC	90678
rs772059949	snp	G/T	3.35982e-05	0.00409853	intron-variant	LRSAM1	GRCh38.p7	9:127457266	GCCCTTAGCCTGCCC[G/T]GCCTGCTGCTCTTCC	90678
rs772067610	snp	C/T	0.000232972	0.0107904	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127481198	ACAAAAGAAAAGCTC[C/T]GAGATTTTGAAATCG	90678
rs772085570	snp	A/C			intron-variant	LRSAM1	GRCh38.p7	9:127473474	CCAAGGTCTCACATT[A/C]AGGGAATTATTGGTA	90678
rs772129554	snp	C/T	5.1387e-05	0.00506862	intron-variant, utr-variant-5-prime	LRSAM1	GRCh38.p7	9:127454485	TCCCTAACTTCTCTC[C/T]TGTGCCCCAGGGTCC	90678
rs772138672	snp	C/G	1.64906e-05	0.00287142	intron-variant	LRSAM1	GRCh38.p7	9:127461152	AGCCACTGCGCCTGG[C/G]TGCCTCTTCCTCTTT	90678
rs772146167	snp	G/T	1.72764e-05	0.00293903	utr-variant-5-prime, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451350	TCGGATGAACCCGGA[G/T]TCGGGACGACCGAAG	90678
rs772168876	snp	C/T	1.70618e-05	0.00292072	intron-variant	LRSAM1	GRCh38.p7	9:127491310	GGTATGTAGGGCTCC[C/T]TGCCCCTGCCCTCCT	90678
rs772178423	snp	A/C			intron-variant	LRSAM1	GRCh38.p7	9:127472733	CCTTGCTTTTTTTGT[A/C]TCTCAAGAAAAGTCT	90678
rs772199579	in-del	-/G	3.10482e-05	0.00393994	intron-variant	LRSAM1	GRCh38.p7	9:127483035	TGTGAGTTTTGGGAT[-/G]GGGAGCTTGTGAGCA	90678
rs772202137	snp	C/T	9.88598e-05	0.00702995	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127461243	TGACCCAGCTCCAGA[C/T]TCTCAATGTTAAAGG	90678
rs772230684	snp	A/G	3.8981e-05	0.00441463	intron-variant	LRSAM1	GRCh38.p7	9:127492773	CTGCCGCCAGCTCAC[A/G]GTGGTGCGGGGTGTG	90678
rs772261735	in-del	-/TG	0.00107143	0.0231207	intron-variant	LRSAM1	GRCh38.p7	9:127473962	TGCTGCACGCATACA[-/TG]TGTGTGTGTGTGCGT	90678
rs772262586	snp	C/G			intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127449924	CAATGTAACCTAGAC[C/G]CCCTCCTAAGTGCCC	90678
rs772266627	snp	A/G	1.6607e-05	0.00288153	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127501110	AGAGCTGGAGGTGCA[A/G]GCCTCAGAGTGTGTC	90678
rs772268890	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127484749	CTACAAATGTGTGTG[C/T]ACAAACATCTATTCT	90678
rs772281232	snp	C/T	1.65274e-05	0.00287462	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127501035	ACCAATGGGTGAGGT[C/T]GTCACCCCTACGGCC	90678
rs772299826	snp	C/T	1.64904e-05	0.00287139	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127479393	TGCAGGAACAGAAGA[C/T]GCTGGAGAAACTCGA	90678
rs772319955	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127486311	GTTGGGGGTGGGATG[C/T]CCTGGAAGGATAAGT	90678
rs772393422	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127470510	ACACAGAGCCAGACC[A/G]TATCAATGCCCAATG	90678
rs772577965	snp	C/T	1.64751e-05	0.00287007	intron-variant	LRSAM1	GRCh38.p7	9:127455533	AGAACAAGCTAAAAA[C/T]TGGCAGGAGGGGAGA	90678
rs772587703	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127467545	AAAACAAGGTAGGGC[A/G]TCACACTGCCTGCCT	90678
rs772592309	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127477485	CCAGGCGCAGTGGCT[C/T]ACGCCTATAATCCCA	90678
rs772644990	snp	A/G	1.64909e-05	0.00287144	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127485786	AACCGGCTCATCCAG[A/G]TGGCCTACGAATCTC	90678
rs772648927	snp	C/G	1.70997e-05	0.00292396	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127495988	ATGGAGCGCCAGCTG[C/G]TGGCCCTCCTGGAGG	90678
rs772694261	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127455767	CAGCAGGTGTTTTCA[C/T]AGATAGGAGAGTAGG	90678
rs772728896	snp	G/T			intron-variant	LRSAM1	GRCh38.p7	9:127489047	GTATCTGTGGAGCTT[G/T]TCTGAGGAAAATTCT	90678
rs772739566	snp	C/T	9.88696e-05	0.00703029	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127462302	GAGCTTCGAAGCCTG[C/T]GTACCCTCAACATCA	90678
rs772764948	snp	A/G	6.47983e-05	0.00569166	intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127450718	AAAATGCCCCTTGGA[A/G]GGGATAACGTACCAG	90678
rs772786050	snp	C/G/T	0.000110566	0.00743453	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127502873	CAGGACATCGCCCAG[C/G/T]GCCTCCGCATCTACC	90678
rs772793971	snp	C/T	0.000236867	0.0108801	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127492886	CGAGAGGAAGAGCTC[C/T]GGGAAATCCTGGTAT	90678
rs772819401	snp	C/T	3.40959e-05	0.00412878	intron-variant	LRSAM1	GRCh38.p7	9:127479826	GGCTCAGGACCCCTA[C/T]CTCCGGCTGCAGGAG	90678
rs772839441	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127468300	TCAGTCATTAGGCTG[C/T]AGGGAGGAGAAGGGA	90678
rs772858883	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127480430	GCTGGGGAGACATGG[C/T]GCCAGAAAAGCCTGA	90678
rs772879678	in-del	-/TTTTTTTTTTTTC			intron-variant	LRSAM1	GRCh38.p7	9:127466519	ATTTTTTTTTTTTTT[-/TTTTTTTTTTTTC]CACTAGAGATGGGGT	90678
rs772884032	snp	C/T	3.4984e-05	0.0041822	intron-variant	LRSAM1	GRCh38.p7	9:127502758	CCAGCCACATGCTCC[C/T]GCTCTCCCTCCCCAG	90678
rs772907487	snp	G/T	1.64751e-05	0.00287007	intron-variant	LRSAM1	GRCh38.p7	9:127479535	TGCTAGGGTCCAGCC[G/T]GGCTGCATCCCCCAG	90678
rs772921947	snp	G/T			intron-variant	LRSAM1	GRCh38.p7	9:127498377	CTCTCAGACTGGAGA[G/T]CAGAAGAGTTTTCCA	90678
rs772922921	snp	C/T	3.99616e-05	0.00446981	intron-variant	LRSAM1	GRCh38.p7	9:127487773	CAGGAGGTGAGCCCT[C/T]GCCCAGAGCCTGAGG	90678
rs772924133	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127481730	GAGACATGAATAAGG[C/T]TAGATATATAATGTC	90678
rs773006044	in-del	-/A			intron-variant	LRSAM1	GRCh38.p7	9:127463198	GCAAGACTTTGTCTC[-/A]AAAAAAAAAAAAAAA	90678
rs773054935	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127467308	TAAACTATCACAAAG[A/G]GATAAATGCAGGGGC	90678
rs773079631	snp	A/G	1.72543e-05	0.00293715	intron-variant	LRSAM1	GRCh38.p7	9:127496126	CTGCATGGAGGGGAG[A/G]GGCACGCAAGGCCGC	90678
rs773122117	snp	A/G	1.66424e-05	0.0028846	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127481199	CAAAAGAAAAGCTCC[A/G]AGATTTTGAAATCGC	90678
rs773171244	in-del	-/TGTGTGTGCGTGTGCATGTA	2.92112e-05	0.00382161	intron-variant	LRSAM1	GRCh38.p7	9:127473964	CTGCACGCATACATG[-/TGTGTGTGCGTGTGCATGTA]TGTGTGTGTGCGTGT	90678
rs773219344	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127482433	CAGGTGTGAGCCACC[A/G]CACCCGGCCATGTGA	90678
rs773228860	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127478857	TAACATCAGGCCACC[C/T]GGGGGTTCCTGGTGC	90678
rs773271495	snp	A/G	1.67913e-05	0.00289748	intron-variant	LRSAM1	GRCh38.p7	9:127457271	TAGCCTGCCCTGCCT[A/G]CTGCTCTTCCTCAGC	90678
rs773280050	snp	C/T	5.65328e-05	0.00531632	intron-variant	LRSAM1	GRCh38.p7	9:127492780	CAGCTCACGGTGGTG[C/T]GGGGTGTGGTCTTGT	90678
rs773297136	in-del	-/GGCTG	2.79162e-05	0.00373595	intron-variant	LRSAM1	GRCh38.p7	9:127483062	AGCACGCTGCCTGCT[-/GGCTG]GGCTGGCAGGGTGGA	90678
rs773305807	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127500216	AGATACAAAAATTAG[C/T]CTGTCGTGATAGTGG	90678
rs773338197	snp	A/G			upstream-variant-2KB, intron-variant	RPL12, LRSAM1	GRCh38.p7	9:127453282	AGACGGGGTTTGACC[A/G]TGTTACCCAGGCTGG	90678
rs773392393	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127467855	GGCCGCTGCCTCCTC[C/T]CCTCATTGAGGAACT	90678
rs773421954	snp	C/T	1.73186e-05	0.00294261	utr-variant-5-prime, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451352	GGATGAACCCGGATT[C/T]GGGACGACCGAAGGA	90678
rs773440440	snp	A/G	1.7065e-05	0.00292099	missense, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451313	GGGTCGAACTTCGGC[A/G]GCATGGTGGAGGCGG	90678
rs773487480	snp	C/G	1.66394e-05	0.00288434	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127501117	GAGGTGCAGGCCTCA[C/G]AGTGTGTCGTGTGCC	90678
rs773494255	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127486942	AATCCCAGCACTTTG[A/G]GAGGCCGAGGTGGGT	90678
rs773501080	snp	C/T	1.64795e-05	0.00287045	intron-variant	LRSAM1	GRCh38.p7	9:127461169	GCCTCTTCCTCTTTC[C/T]TAGGTCTTAAACGTG	90678
rs773505699	snp	C/T	4.95782e-05	0.00497862	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127501046	AGGTCGTCACCCCTA[C/T]GGCCCCCCAGGAGCC	90678
rs773546358	snp	C/G	3.4146e-05	0.00413181	intron-variant	LRSAM1	GRCh38.p7	9:127491312	TATGTAGGGCTCCCT[C/G]CCCCTGCCCTCCTTC	90678
rs773571707	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127485857	TAAGGAAGAGGAGTC[C/T]CAGGTGAGGGAGCTG	90678
rs773572737	snp	A/G	1.64906e-05	0.00287142	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127479394	GCAGGAACAGAAGAT[A/G]CTGGAGAAACTCGAG	90678
rs773576870	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127497110	CTCATCCTGACCGTG[C/G]GCCCCGCCAGGCCCC	90678
rs773597050	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127477507	ATAATCCCAGCACTT[C/T]GGGAGGCCGAGTCGG	90678
rs773610017	multinucleotide-polymorphism	CC/TT			intron-variant, utr-variant-5-prime	LRSAM1	GRCh38.p7	9:127454070	ACGCAGCCCCTGCCC[CC/TT]GTGGAACTCACTAGA	90678
rs773718248	snp	A/G	1.64751e-05	0.00287007	intron-variant	LRSAM1	GRCh38.p7	9:127455538	AAGCTAAAAACTGGC[A/G]GGAGGGGAGACACTT	90678
rs773856728	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127497650	CACTGAGGGACTTTG[A/G]ACTAGAGGGAGAAAT	90678
rs773871374	snp	C/T	1.68678e-05	0.00290407	intron-variant	LRSAM1	GRCh38.p7	9:127479522	TTTGTGAGCCGCCTG[C/T]TAGGGTCCAGCCTGG	90678
rs773872698	snp	G/T	1.65015e-05	0.00287237	synonymous-codon, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127449651	GTTTCACTGTAATCC[G/T]CAGGCCCTTCCAGTC	90678
rs773879439	snp	A/G			intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127450340	GCTAGGTTTACATCT[A/G]CAACACAGCTGGAAA	90678
rs773889029	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127455660	GACTTTCTTGTTGCA[C/T]GTCTGCTTGTTTGAA	90678
rs773899723	snp	C/T	3.37519e-05	0.00410789	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127501138	GTCGTGTGCCTGGAA[C/T]GGGAGGTAAGTCCGG	90678
rs773902383	in-del	CCGTGGAACTCACTAGAAAGACGCAGCCCCTGCCCCC/TT			intron-variant, utr-variant-5-prime	LRSAM1	GRCh38.p7	9:127454070	ACGCAGCCCCTGCCC[lengthTooLong]GTGGAACTCACTAGA	90678
rs773964188	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127466723	GTATTTATCCAAAGT[C/G]AACTGAGAGGCTGGG	90678
rs773965364	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127480297	GGGATCACATCCTGC[C/T]CCAGTATTTTGGGTT	90678
rs773966536	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127492585	CATTGTCATCAGTCA[C/T]CAGGATCCCATGCCT	90678
rs774007889	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127457876	AGCACAGGTGTCAGC[C/T]CAGCAGCACAGGCCC	90678
rs774062037	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127465283	ATGAGAATGCTCTAT[A/G]ATCTGTGCAGCCAAC	90678
rs774147644	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127479175	CTGAGGCTCAGAGGG[A/G]TTGAGCCCAGCACCG	90678
rs774230694	snp	A/G	1.68542e-05	0.0029029	intron-variant	LRSAM1	GRCh38.p7	9:127491302	TCACTCCAGGTATGT[A/G]GGGCTCCCTGCCCCT	90678
rs774298357	snp	A/G	6.90727e-05	0.00587636	utr-variant-5-prime, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451347	GTGTCGGATGAACCC[A/G]GATTCGGGACGACCG	90678
rs774397782	snp	G/T	1.66424e-05	0.0028846	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127481196	AGACAAAAGAAAAGC[G/T]CCGAGATTTTGAAAT	90678
rs774399646	snp	A/G	0.000115638	0.00760299	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127467775	GGCCATGGTCTACCC[A/G]CCGCGGGAGGTGTGT	90678
rs774505948	snp	C/T	3.30306e-05	0.00406377	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127479947	CAGAACATTTCCAGC[C/T]GGATCCAGAAGCTGC	90678
rs774532306	in-del	-/TCTGACATGGCAGAAACTGTTTTAGAGAA	5.33035e-05	0.00516226	frameshift-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127450733	GGGATAACGTACCAG[lengthTooLong]ACCCAGGGGGCCGAT	90678
rs774538227	snp	A/G	1.64773e-05	0.00287026	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127473919	ATTCTCAAGGGAGGA[A/G]TTAGAGTGGCAGGTA	90678
rs774575806	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127462750	ACCTGGGTGATGGGA[C/T]GATCTGTGCAGCAAA	90678
rs774638544	snp	G/T			intron-variant	LRSAM1	GRCh38.p7	9:127496999	GTTGCTAGTGCTGGT[G/T]TCCCTTTGGGCCTCA	90678
rs774644108	snp	A/G	6.59033e-05	0.00573997	intron-variant	LRSAM1	GRCh38.p7	9:127478884	GTGCCCATGCCAGGG[A/G]GAACCACTGCTGCCA	90678
rs774658208	in-del	-/TTAT			intron-variant	LRSAM1	GRCh38.p7	9:127481994	TTCTGGAAAGAAAAA[-/TTAT]TTAGTTACATAAATT	90678
rs774697286	snp	C/T	1.65701e-05	0.00287833	intron-variant	LRSAM1	GRCh38.p7	9:127485701	CCCCAGGAGCAGCCA[C/T]TCCACTCAGCTGTCC	90678
rs774722158	snp	C/G	1.64746e-05	0.00287002	intron-variant	LRSAM1	GRCh38.p7	9:127462386	GAGGTAAATGGGAAG[C/G]TGTTCTTGCCTGGGG	90678
rs774735924	snp	A/C/T	9.89387e-05	0.00703282	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127485779	CTGTAAGAACCGGCT[A/C/T]ATCCAGATGGCCTAC	90678
rs774763402	in-del	-/AT	1.65307e-05	0.0028749	intron-variant	LRSAM1	GRCh38.p7	9:127473961	CTGCTGCACGCATAC[-/AT]ATGTGTGTGTGTGCG	90678
rs774800333	in-del	-/AGCT			intron-variant	LRSAM1	GRCh38.p7	9:127490089	GGCTGCTGACCTTCA[-/AGCT]AGCCTTGGGCAAGCC	90678
rs774848483	in-del	-/CAA			intron-variant	LRSAM1	GRCh38.p7	9:127463198	AGCAAGACTTTGTCT[-/CAA]AAAAAAAAAAAAAAA	90678
rs774887607	snp	A/G	1.64963e-05	0.00287192	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127485804	GCCTACGAATCTCAG[A/G]GGCAGAACTTGGTCC	90678
rs774924873	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127492661	GCAGAAGGGCCTCTT[A/G]GCTTTGTCCCCCAAC	90678
rs774936278	snp	C/T	1.70194e-05	0.00291709	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127454594	CTGGAGTACCAGATG[C/T]GTTTGGTGAGGGAAA	90678
rs775001547	snp	G/T	2.13463e-05	0.00326691	intron-variant, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127487649	GAAACGTTCCAAGAA[G/T]GAATGAATTTGCTGT	90678
rs775020499	snp	A/G	4.71254e-05	0.00485391	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127467764	CTTGACGCCTCGGCC[A/G]TGGTCTACCCGCCGC	90678
rs775044253	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127463372	GCTGGGAGGGAGAGA[A/G]GGAGGTAGGGAGCCG	90678
rs775045841	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127495845	TATGAGTTTTTGTAG[A/G]AAAAATCCCGAGTAC	90678
rs775061917	snp	C/G	1.65965e-05	0.00288062	intron-variant	LRSAM1	GRCh38.p7	9:127495313	TTGCCTGCTTCATTC[C/G]TGGCAGACGGAGTTA	90678
rs775108432	snp	A/G	3.30497e-05	0.00406494	intron-variant	LRSAM1	GRCh38.p7	9:127479996	TGGGCTCTGCTCCTC[A/G]GCCCCAGCCCCAGAG	90678
rs775109275	snp	A/G	8.23716e-05	0.00641709	intron-variant	LRSAM1	GRCh38.p7	9:127455544	AAAACTGGCAGGAGG[A/G]GAGACACTTACTCTT	90678
rs775125689	snp	A/G	1.64727e-05	0.00286986	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127455045	CATCTCTAAATGTGA[A/G]CTCTCAGAGGTAAAC	90678
rs775210983	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127492400	GTTTCCAAGAGCAGG[C/T]GCAGGAGTGAAGCAG	90678
rs775218956	snp	A/T			intron-variant	LRSAM1	GRCh38.p7	9:127481765	TATATTCCTAGTATA[A/T]AAAGTTCAGGCCAGG	90678
rs775297627	snp	A/G/T	1.67964e-05	0.00289792	intron-variant	LRSAM1	GRCh38.p7	9:127491184	GTGGTTAATGTGAGT[A/G/T]AAAAAAAACCCTGTC	90678
rs775302920	snp	C/T	3.7059e-05	0.00430443	intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127450846	GTGCAGAGGGAGCCC[C/T]GAGCCACAGCCCTCT	90678
rs775318697	snp	C/T	1.6476e-05	0.00287014	intron-variant	LRSAM1	GRCh38.p7	9:127462423	CTGGCCTGCCCACCT[C/T]CCCTCTCTCCCACAT	90678
rs775386606	snp	G/T			intron-variant	LRSAM1	GRCh38.p7	9:127482288	GCTGGGATTATAGGC[G/T]CATACCACCAGGTCC	90678
rs775480266	snp	C/T	6.62844e-05	0.00575655	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127479927	AGCAGCTGAAGCAGA[C/T]GGAACAGAACATTTC	90678
rs775492520	snp	A/G	1.7009e-05	0.0029162	missense, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451299	CTTTGATCTCGTTGG[A/G]GTCGAACTTCGGCGG	90678
rs775498941	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127483497	ATAGAGGATTGTTTA[A/G]ATAAATGTTGGTGAT	90678
rs775636699	snp	C/T	2.81583e-05	0.00375211	intron-variant	LRSAM1	GRCh38.p7	9:127489532	AGGTGAGCGCTGGGG[C/T]TGGGGTCCCTGGACC	90678
rs775655109	snp	A/G	2.6623e-05	0.0036484	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127489452	GTTGCAGAGCGCGAT[A/G]CAGAAGGCTGCGTTC	90678
rs775655255	snp	A/C/T	5.09561e-05	0.00504737	intron-variant	LRSAM1	GRCh38.p7	9:127497371	CTTCCAGGCAGGGCT[A/C/T]CAGCCGTATGTGTGG	90678
rs775659934	snp	A/G	3.295e-05	0.00405881	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127473900	CTGATGGGCCCACGG[A/G]CAGATTCTCAAGGGA	90678
rs775740396	snp	C/G	3.36791e-05	0.00410346	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127492874	GAGAAGCAGCAGCGA[C/G]AGGAAGAGCTCCGGG	90678
rs775743246	snp	A/G	1.65979e-05	0.00288074	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127497293	AGCACGAGATCCTCC[A/G]GAGAGTCCAGGAACT	90678
rs775747767	snp	C/T	8.29593e-05	0.00643994	intron-variant	LRSAM1	GRCh38.p7	9:127485688	CCCTGCCCAGGTGCC[C/T]CAGGAGCAGCCACTC	90678
rs775813333	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127460213	CCATGTTCACCAGGA[C/T]GGTCTCAATCTCCTG	90678
rs775843516	in-del	-/T	0.000331367	0.0128675	intron-variant	LRSAM1	GRCh38.p7	9:127491182	TGTGGTTAATGTGAG[-/T]TAAAAAAAAACCCTG	90678
rs775848557	snp	G/T	3.29609e-05	0.00405948	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127462285	TTCCAGACACCGTGG[G/T]GGAGCTTCGAAGCCT	90678
rs775881443	snp	A/G			upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451447	TATAGGCAGGAAAAC[A/G]CGGCTATCGCGAGAA	90678
rs775895004	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127488880	ACAGACATGAGCCAC[C/G]GGCCTGTTCAGCTCT	90678
rs775965001	in-del	-/C	1.65303e-05	0.00287487	frameshift-variant, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127501048	TCGTCACCCCTACGG[-/C]CCCCCCAGGAGCCTC	90678
rs776038284	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127460534	CCAAGTCTGTAGTCC[C/T]CTTCTCCCTCCTTCC	90678
rs776039231	snp	A/G	6.72438e-05	0.00579805	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127454577	AGGAGGCTCGGAAAC[A/G]CCTGGAGTACCAGAT	90678
rs776070153	snp	C/G			upstream-variant-2KB, intron-variant	RPL12, LRSAM1	GRCh38.p7	9:127453164	TTGGCTCACTGCAAC[C/G]TCTGCCTCCTGGGTT	90678
rs776091047	in-del	-/AC			intron-variant	LRSAM1	GRCh38.p7	9:127465918	TCCTGGGCTTCATAA[-/AC]ACGGAGGCATCTGCA	90678
rs776125314	snp	C/G	1.67871e-05	0.00289711	utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127454522	TCGCTCTGGGAAAAG[C/G]GAAGGATGCCGCTCT	90678
rs776143892	snp	A/G	1.65026e-05	0.00287246	intron-variant	LRSAM1	GRCh38.p7	9:127461277	GGACCAAGAAGCCGT[A/G]TCCGTGTGACCCTCC	90678
rs776157689	snp	A/G	1.67685e-05	0.00289551	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127479903	ACGCAGAGCGGCAGC[A/G]GCTGCAGGAGCAGCT	90678
rs776159152	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127476113	TACCCAAGATAAATG[C/T]TTGCATGAGGAGACA	90678
rs776169634	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127493123	CTGGAGTGCAGTGGC[A/G]CAATCTCAGCTCACT	90678
rs776180165	snp	C/G			intron-variant, utr-variant-5-prime	LRSAM1	GRCh38.p7	9:127453602	TGGCAGAGTCTGTTA[C/G]AGTCCTCAAAGAACA	90678
rs776184530	snp	C/T	0.000116472	0.00763036	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127502878	CATCGCCCAGCGCCT[C/T]CGCATCTACCACAGC	90678
rs776197379	in-del	-/C			intron-variant	LRSAM1	GRCh38.p7	9:127466531	TTTTTTTTTTTTTTT[-/C]CACTAGAGATGGGGT	90678
rs776213635	snp	A/G	1.75813e-05	0.00296485	intron-variant	LRSAM1	GRCh38.p7	9:127495917	CTGTTGTAAACAGTG[A/G]GTTCTTTTCTTCCTT	90678
rs776213754	snp	C/T	1.65644e-05	0.00287783	intron-variant	LRSAM1	GRCh38.p7	9:127485706	GGAGCAGCCACTCCA[C/T]TCAGCTGTCCCCACC	90678
rs776224600	snp	G/T	8.43206e-05	0.00649255	utr-variant-3-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127502947	CCTGCCTCGGCCACT[G/T]TGAGCCCCGGGCTCC	90678
rs776245063	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127489915	CAGACAGACAGAGGC[A/G]TCTCAGGGGCATATA	90678
rs776247817	snp	A/G	4.96746e-05	0.00498346	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127489503	AGACCTGATGCATCG[A/G]CAGATCAGGAGCCAG	90678
rs776291709	snp	A/T			intron-variant	LRSAM1	GRCh38.p7	9:127454870	GGTTCACCTGCCAAA[A/T]GGACCAGTGGAACCA	90678
rs776292756	in-del	-/AA	1.70272e-05	0.00291776	intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127450693	CGCTTAAAGTGAAAC[-/AA]ATGTGAAAAAAATGC	90678
rs776298301	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127469789	TAACACAGTGAAACC[C/T]TGTCTCTACTAAAAA	90678
rs776299591	snp	A/C	1.65403e-05	0.00287574	missense, intron-variant, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127495324	ATTCCTGGCAGACGG[A/C]GTTAGAAGCCAAAAG	90678
rs776366381	snp	A/G	1.67643e-05	0.00289515	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127479841	CCTCCGGCTGCAGGA[A/G]CAGTCCCGGCTGGAG	90678
rs776393347	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127468348	GAGTGCAGGACAGGG[A/G]ACCAGTTAGGAGGCT	90678
rs776409019	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127502351	GGTGGTCAAATGCCC[A/G]AAGGCCCCACTATCA	90678
rs776448720	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127473743	AGTGGGAGCGGGTGT[C/T]TCTGGGTACCTCAGC	90678
rs776477474	snp	A/T			intron-variant	LRSAM1	GRCh38.p7	9:127482067	TGAATAATATTTCTC[A/T]TTAAGGGAAAACATA	90678
rs776505499	snp	G/T			intron-variant	LRSAM1	GRCh38.p7	9:127486482	ACAGGCCAGCAGCCC[G/T]GGATGCCCTGTTTTT	90678
rs776538440	snp	A/G	1.64749e-05	0.00287005	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127473811	TACAGAGTCAGGGCT[A/G]GAATACTACCCCCCT	90678
rs776645617	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127494561	ACGCCTGTTGTCACC[A/G]TGGCTGTTATCAGCA	90678
rs776691533	in-del	-/G	1.66258e-05	0.00288316	intron-variant	LRSAM1	GRCh38.p7	9:127497241	AGTCTGCACTTCCTT[-/G]AACTGTCACAGGTGG	90678
rs776694291	snp	C/G	9.41708e-05	0.00686124	synonymous-codon, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127450752	CAGGGGGCCGATCTT[C/G]GGGGCCAGGGCAGAA	90678
rs776726818	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127488675	CACAGTTCACTGCAG[C/T]CTCAAACTCCTGGGC	90678
rs776761131	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127460049	TCTATCACCAGGCTG[C/G]AGTGCAGTGGTGTGA	90678
rs776814240	snp	C/G	8.868e-05	0.00665824	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127482963	AGAATAAGAATGGAA[C/G]AGTTGATGTCCATAA	90678
rs776821362	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127460076	GTGATCTCGGCTCAC[C/T]GCAATCTCCACCTCC	90678
rs776877360	snp	A/G	1.75075e-05	0.00295862	intron-variant	LRSAM1	GRCh38.p7	9:127467864	CTCCTCCCCTCATTG[A/G]GGAACTATGACCCCC	90678
rs776894109	snp	A/G	9.99267e-05	0.00706777	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127481213	CGAGATTTTGAAATC[A/G]CTGGAAAATGAAAGG	90678
rs776906785	snp	A/T	1.68119e-05	0.00289926	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127492858	CCAGCAGCTGCTCAA[A/T]GAGAAGCAGCAGCGA	90678
rs776922280	snp	A/G	5.07078e-05	0.00503501	utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127454509	AGGGTCCTAAAGATC[A/G]CTCTGGGAAAAGGGA	90678
rs776945907	snp	C/G			intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127450113	AGCCTCAACAGGAGG[C/G]TAAGTGTCCCTTAAG	90678
rs777008476	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127487066	GTGGGCGCCTGTAAT[C/G]CCAGCTACTTGGGAG	90678
rs777106016	in-del	-/ACGTTGGCTCA			intron-variant	LRSAM1	GRCh38.p7	9:127500087	ACTTAGCAGCCGGGC[-/ACGTTGGCTCA]CGCCTGTAATCCCAG	90678
rs777111007	snp	G/T	3.33528e-05	0.00408354	intron-variant	LRSAM1	GRCh38.p7	9:127497220	GCGGGCTCCCGCCCA[G/T]GCCACAGTCTGCACT	90678
rs777119833	snp	A/C/G			intron-variant	LRSAM1	GRCh38.p7	9:127469648	AAAAAACTTCCTGCT[A/C/G]ACAAGTCAACCAGAA	90678
rs777143742	snp	G/T	1.65209e-05	0.00287405	missense, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127449626	TGGGCCTGTCTGTTC[G/T]GAATGGTCAGTTTCA	90678
rs777176170	in-del	-/G	5.3056e-05	0.00515026	intron-variant	LRSAM1	GRCh38.p7	9:127489527	AGCCAGGTGAGCGCT[-/G]GGGGCTGGGGTCCCT	90678
rs777233045	snp	C/T	1.65304e-05	0.00287488	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127501049	TCGTCACCCCTACGG[C/T]CCCCCAGGAGCCTCC	90678
rs777249094	snp	A/G	1.66999e-05	0.00288958	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127479502	CCTTCAGACGGTCAA[A/G]GAGGTTTGTGAGCCG	90678
rs777258533	snp	G/T	1.6591e-05	0.00288015	intron-variant	LRSAM1	GRCh38.p7	9:127500970	GGGTTAGGGTCAGCG[G/T]AGATGACCCTGGCTC	90678
rs777339104	snp	A/C	3.29875e-05	0.00406112	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127479408	TGCTGGAGAAACTCG[A/C]GTTTGAACGGCGCCT	90678
rs777351976	snp	C/G			utr-variant-3-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127503163	ACCCGAGCCTGGGAG[C/G]CAGCGTCCCAGCCTA	90678
rs777372780	snp	C/T	2.45378e-05	0.00350261	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127489496	TGAAGAAAGACCTGA[C/T]GCATCGGCAGATCAG	90678
rs777407902	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127495706	CAGCACCTGCGGGGA[C/T]AGAGAGGCAGTTGAA	90678
rs777419749	snp	A/G	5.59926e-05	0.00529086	intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127450840	GTGTCTGTGCAGAGG[A/G]AGCCCCGAGCCACAG	90678
rs777423758	in-del	-/GAGAG			downstream-variant-500B	LRSAM1	GRCh38.p7	9:127503630	CGCCGCACCTCAGTC[-/GAGAG]GAGAGGTCAGGTAGG	90678
rs777427283	in-del	-/TT			intron-variant	LRSAM1	GRCh38.p7	9:127482141	AATTTTTAGTATATC[-/TT]TTTTTTTTTTTTTTT	90678
rs777489626	snp	A/T	1.64955e-05	0.00287184	intron-variant	LRSAM1	GRCh38.p7	9:127473951	GACAAGGCAGCCTGC[A/T]GCACGCATACATGTG	90678
rs777496535	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127494497	ATTAATGATGGCATC[A/G]TTAGGTGCACAGCAT	90678
rs777538660	snp	C/T	0.000136916	0.0082728	intron-variant	LRSAM1	GRCh38.p7	9:127497348	AGGTACAAGCACAGC[C/T]CCAGCCTCTTCCAGG	90678
rs777559757	snp	C/T	1.65012e-05	0.00287234	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127459007	TTCTTCTGCAGGTTC[C/T]AGATCTCCACGATAA	90678
rs777564486	in-del	-/GTCTGC	1.64905e-05	0.00287141	intron-variant	LRSAM1	GRCh38.p7	9:127455661	ACTTTCTTGTTGCAT[-/GTCTGC]TTGTTTGAACCCACA	90678
rs777564847	snp	A/T	0.000298383	0.0122107	intron-variant	LRSAM1	GRCh38.p7	9:127483042	TTTGGGATGGGGAGC[A/T]TGTGAGCACGCTGCC	90678
rs777583116	snp	C/G/T	3.74976e-05	0.00432986	intron-variant	LRSAM1	GRCh38.p7	9:127492943	CACAGGCATTTGCTT[C/G/T]TCTTTAACAGACTTG	90678
rs777594391	snp	A/G	3.68521e-05	0.0042924	intron-variant	LRSAM1	GRCh38.p7	9:127457442	TGCATGGGGTTCCAC[A/G]CGGCAGCTGAGCGCC	90678
rs777755879	snp	A/C	3.29484e-05	0.00405871	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127473883	GAACTCTCGGGACAG[A/C]CCTGATGGGCCCACG	90678
rs777775831	snp	A/G	9.60938e-05	0.00693092	intron-variant	LRSAM1	GRCh38.p7	9:127482908	GGGATTCCCTGTTGG[A/G]AATGTTAAATTTGCT	90678
rs777784051	snp	A/G	8.34662e-05	0.00645958	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127454550	TCTTCTTCCGGAAGC[A/G]GAAACCCAGTGAGGA	90678
rs777789178	snp	A/G	1.92029e-05	0.00309856	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127502830	CCAGCAGTGCTGCCA[A/G]CCACTGCGCACCTGC	90678
rs777815906	in-del	-/TTCTTCC	1.75443e-05	0.00296173	intron-variant	LRSAM1	GRCh38.p7	9:127495924	AAACAGTGGGTTCTT[-/TTCTTCC]TTCCTGCTCATGGTA	90678
rs777820148	in-del	-/C			intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127449512	AGGTGAAATCACTCT[-/C]GGCTCACCACTGGTG	90678
rs777840588	snp	C/G	1.64776e-05	0.00287028	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127461245	ACCCAGCTCCAGACT[C/G]TCAATGTTAAAGGTA	90678
rs777867965	snp	A/G	5.05941e-05	0.00502936	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127492840	GGCCCTCAGCTCCCT[A/G]CTCCAGCAGCTGCTC	90678
rs777868589	snp	C/T	1.71026e-05	0.00292421	intron-variant, utr-variant-5-prime	LRSAM1	GRCh38.p7	9:127454491	ACTTCTCTCCTGTGC[C/T]CCAGGGTCCTAAAGA	90678
rs777871553	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127498127	GCCAGAGCCAAGGAA[A/G]AAGCGGAGGAGCTGA	90678
rs777888633	snp	A/G	0.000168036	0.0091646	intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127449725	TAGAAATAAAGGCAT[A/G]TAATCAACATGGTGT	90678
rs777905964	snp	A/G			intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127450919	TCGAAACAGCACAGA[A/G]CGCGAGGCGGGCCAC	90678
rs777946282	snp	A/G	1.64901e-05	0.00287137	intron-variant	LRSAM1	GRCh38.p7	9:127462240	TGAGCTGTGCTATTG[A/G]GGTCTCTGCAGACAA	90678
rs777949013	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127486348	GTTGCTTTCATGCTG[A/G]TGGCTGCTCTGGGGT	90678
rs777978586	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127488416	ACGGGCACCCACCAA[C/T]ACGCCCAACTAATTT	90678
rs777987106	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127467584	CCCAGGCACTGGGAA[C/T]GCAGCTGTAAGTAAC	90678
rs778123569	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127472665	ATAAATAAATAAAAA[C/T]AAAAATAAACATTAA	90678
rs778141208	snp	A/G	1.73267e-05	0.0029433	intron-variant	LRSAM1	GRCh38.p7	9:127479790	GTCAGTACCCCTCAC[A/G]GCGTCTGAGGGGGTC	90678
rs778157640	snp	G/T	1.65343e-05	0.00287521	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127479460	CACCCAGCTCCTTCA[G/T]CAGAGCAGCAGCCAG	90678
rs778245007	snp	C/T	1.65707e-05	0.00287838	synonymous-codon, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127449616	AGCAAATACCTGGGC[C/T]TGTCTGTTCTGAATG	90678
rs778245433	snp	A/G	1.78678e-05	0.00298891	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127487728	TCGTGGCAGCAAATG[A/G]ATCAGAACAAAGCCA	90678
rs778245782	snp	A/G	1.64803e-05	0.00287052	intron-variant	LRSAM1	GRCh38.p7	9:127455645	AGCTTCATCTTCAGA[A/G]ACTTTCTTGTTGCAT	90678
rs778338519	snp	A/G	1.79242e-05	0.00299362	intron-variant	LRSAM1	GRCh38.p7	9:127457435	GGGGCTCTGCATGGG[A/G]TTCCACGCGGCAGCT	90678
rs778343243	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127493155	CAGCCTTGACTTCCT[A/G]GGCTCAAGCGATCCT	90678
rs778344326	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127494317	TTGATCCCACTCCCC[A/G]TGTCATGCCAGCCCT	90678
rs778365076	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127460980	CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA	90678
rs778392265	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127457567	GCTGTGTGTGGGTTA[A/G]GGTGACAAAGATGAC	90678
rs778431530	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127492276	AATGATCTCCAGAGA[C/T]GAGGGGACTGGGACT	90678
rs778480290	snp	C/G	3.41588e-05	0.00413258	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127495994	CGCCAGCTGGTGGCC[C/G]TCCTGGAGGAGCTGT	90678
rs778517874	snp	C/T	1.66369e-05	0.00288412	intron-variant	LRSAM1	GRCh38.p7	9:127497234	AGGCCACAGTCTGCA[C/T]TTCCTTGAACTGTCA	90678
rs778570971	in-del	-/GTTGCATGTCTGC	6.59261e-05	0.00574097	intron-variant	LRSAM1	GRCh38.p7	9:127455654	TTCAGAGACTTTCTT[-/GTTGCATGTCTGC]TTGTTTGAACCCACA	90678
rs778625125	snp	A/G	1.65425e-05	0.00287593	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127457333	GCTGATCGTCCACAC[A/G]AATCACCTCACTTCC	90678
rs778653636	snp	A/C			intron-variant	LRSAM1	GRCh38.p7	9:127459513	TGTGAGCCACCACGC[A/C]TGACCAATTGTACCA	90678
rs778681615	snp	C/G	6.7643e-05	0.00581523	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127492828	GGAGCAGCGCTGGGC[C/G]CTCAGCTCCCTGCTC	90678
rs778692919	snp	A/G	6.58957e-05	0.00573964	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127473876	GAATCGAGAACTCTC[A/G]GGACAGCCCTGATGG	90678
rs778709280	snp	A/G	3.09411e-05	0.00393314			GRCh38.p7	9:127483035	TGTGAGTTTTGGGAT[A/G]GGGAGCTTGTGAGCA	90678
rs778740625	snp	A/G	3.34102e-05	0.00408705			GRCh38.p7	9:127454544	TGCCGCTCTTCTTCC[A/G]GAAGCGGAAACCCAG	90678
rs778771584	snp	A/C	1.80961e-05	0.00300794	intron-variant	LRSAM1	GRCh38.p7	9:127501165	CCGGGGCCCTCCCCA[A/C]CCGCCTGCCCTGCCT	90678
rs778846891	snp	C/G	1.64746e-05	0.00287002	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127461235	TGGGAACCTGACCCA[C/G]CTCCAGACTCTCAAT	90678
rs778936024	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127488375	CAACTGATTCTCCTG[C/T]CTCAGCCTCCCAAGT	90678
rs778980908	snp	A/G	1.65872e-05	0.00287981	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127501105	CCTGCAGAGCTGGAG[A/G]TGCAGGCCTCAGAGT	90678
rs778996687	snp	A/G	1.64906e-05	0.00287142	splice-acceptor-variant	LRSAM1	GRCh38.p7	9:127479381	GGATCTGTGTCTTGC[A/G]GGAACAGAAGATGCT	90678
rs779016887	snp	A/G	1.64773e-05	0.00287026	intron-variant, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127487628	TGGCACATAGTAGGT[A/G]CTCGGGAAACGTTCC	90678
rs779022904	snp	A/G	1.6477e-05	0.00287024	splice-donor-variant	LRSAM1	GRCh38.p7	9:127455621	GTTCTGCAGAAGAAG[A/G]TAAGATGGAGCTTCA	90678
rs779024386	snp	G/T			intron-variant	LRSAM1	GRCh38.p7	9:127499128	GCTGTAATCCCACAC[G/T]TTGGGAGGCCTACGT	90678
rs779051009	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127479717	TGGGAGGAGCTGGCC[A/G]GAGGTCACACAAAAA	90678
rs779095402	snp	C/T	1.65168e-05	0.00287369	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127479445	GGGGCAGCGGGAGCA[C/T]ACCCAGCTCCTTCAG	90678
rs779139423	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127478539	GAAGTTGTACCCACA[C/T]CTTTGTGCACTGTGA	90678
rs779188065	snp	A/G	3.55303e-05	0.00421472	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127487721	GATTCTGTCGTGGCA[A/G]CAAATGGATCAGAAC	90678
rs779208101	snp	A/C/T	8.37449e-05	0.00647042	intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127449599	TCCCGAAACCAAGCA[A/C/T]AAGCAAATACCTGGG	90678
rs779377549	snp	C/T	1.71522e-05	0.00292845	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127495981	AGAGGGGATGGAGCG[C/T]CAGCTGGTGGCCCTC	90678
rs779388263	snp	A/G	1.64757e-05	0.00287012	intron-variant	LRSAM1	GRCh38.p7	9:127455105	CTGTCCCGTTTTCTT[A/G]GATCTTGTGTCCCTA	90678
rs779392350	snp	G/T			intron-variant	LRSAM1	GRCh38.p7	9:127490714	AATATGATACATCAA[G/T]TGTGCAGCACAGGCC	90678
rs779458921	snp	A/G	1.64787e-05	0.00287038	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127467747	GTCTGCAGATGCTGA[A/G]CCTTGACGCCTCGGC	90678
rs779479903	snp	C/T	1.64844e-05	0.00287087	intron-variant	LRSAM1	GRCh38.p7	9:127473764	GTACCTCAGCTGTCT[C/T]CTCCCTCCTGGTCAG	90678
rs779499213	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127455710	AGCTGTCTTCCCGGC[A/G]TAGACACCTCCTTTC	90678
rs779500141	snp	A/C			intron-variant	LRSAM1	GRCh38.p7	9:127470323	ACAGGGCAGCAGGAG[A/C]GAGAATTAGTGCCAA	90678
rs779523448	snp	A/T			intron-variant	LRSAM1	GRCh38.p7	9:127459410	TTTTAGTAGAGATGG[A/T]GTTTCGCCTTGTTGG	90678
rs779538129	snp	C/T	1.70359e-05	0.0029185	intron-variant	LRSAM1	GRCh38.p7	9:127495445	TGGTGCCTGTCCCGG[C/T]CAGGGAGCCCTGGGG	90678
rs779569966	snp	C/T	5.38522e-05	0.00518876	intron-variant	LRSAM1	GRCh38.p7	9:127481276	TTTTTTTTTTTGAGA[C/T]GGAGTCCTGCACTGT	90678
rs779611315	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127473246	GTTTACCCCGGAAGG[A/G]CACCATCATCAAAGT	90678
rs779613513	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127457802	GAGGTGTGAGCCCAG[A/G]GTTGTTATGCGCAGA	90678
rs779764391	snp	A/G	1.72513e-05	0.0029369	utr-variant-5-prime, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451343	GCTGGTGTCGGATGA[A/G]CCCGGATTCGGGACG	90678
rs779768682	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127485252	AGCCTTCCAAGCATA[C/T]GTTGCTTTTATAGTT	90678
rs779770233	snp	A/G	4.99147e-05	0.00499549	intron-variant	LRSAM1	GRCh38.p7	9:127481160	CTGGTGACTGCCAGG[A/G]CCTTTTATGATTTTC	90678
rs779786777	snp	A/G	3.49162e-05	0.00417814	utr-variant-5-prime, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451366	TCGGGACGACCGAAG[A/G]AAGTTGCACCTTGGC	90678
rs779873656	snp	A/C/T	6.58962e-05	0.00573974	missense, synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127461226	ACGTTCCATTGGGAA[A/C/T]CTGACCCAGCTCCAG	90678
rs779903349	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127464341	GCAGCCACTGGCCAT[C/G]TGTATCTAATGAGCA	90678
rs779959555	snp	C/G	4.03047e-05	0.00448896	intron-variant	LRSAM1	GRCh38.p7	9:127492765	CTCCTGCGCTGCCGC[C/G]AGCTCACGGTGGTGC	90678
rs780023423	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127483700	ACAAAGTCTCGCTCT[A/G]TTGCTCAGGCTGGAG	90678
rs780051652	in-del	-/AACA	3.38834e-05	0.00411589	intron-variant	LRSAM1	GRCh38.p7	9:127495293	TACCATTTTGTGACT[-/AACA]AACATTGCCTGCTTC	90678
rs780101859	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127478473	ACGGACAGATGTTGA[C/T]AGATGTATGAGTTAT	90678
rs780121774	snp	C/T	1.66335e-05	0.00288383	synonymous-codon, intron-variant, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127491274	GTTAAAGAGGAAGTC[C/T]CTGGACACAGAGTCA	90678
rs780168494	snp	A/G	9.29325e-05	0.00681598	intron-variant	LRSAM1	GRCh38.p7	9:127467719	AGCGAACAGTAAAGC[A/G]GGTTACCCTTGTGTC	90678
rs780173932	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127462645	TTTAAGAAAGTTGTC[A/G]GTAGGGGAACAACAC	90678
rs780200210	snp	C/T	1.67517e-05	0.00289406	intron-variant	LRSAM1	GRCh38.p7	9:127495426	AGCTGCAAGTAAGGA[C/T]TGCTGGTGCCTGTCC	90678
rs780209041	snp	C/T	1.65362e-05	0.00287538	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127501022	CAGAGCTGAAACCAC[C/T]AATGGGTGAGGTCGT	90678
rs780219877	snp	A/G	1.64931e-05	0.00287163	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127485766	TGCTGACTGAGAGCT[A/G]TAAGAACCGGCTCAT	90678
rs780220372	snp	C/T	1.67284e-05	0.00289205	utr-variant-3-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127502920	GCCCGCCCACCTGGG[C/T]CTGGTCCTAGCCCTG	90678
rs780246859	in-del	-/GG			intron-variant	LRSAM1	GRCh38.p7	9:127501295	ATAAAGATGACCCCT[-/GG]GGTCCCATGACCCAA	90678
rs780261397	snp	C/T			downstream-variant-500B	LRSAM1	GRCh38.p7	9:127503808	GGCAGCTGAGGCTGA[C/T]GGGGGTAAATGCTCA	90678
rs780288514	snp	A/G	1.72169e-05	0.00293396	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127495969	TGTCTTGCAGGAAGA[A/G]GGGATGGAGCGCCAG	90678
rs780358722	snp	C/T	1.64738e-05	0.00286995	intron-variant	LRSAM1	GRCh38.p7	9:127455094	GTGAATTGGATCTGT[C/T]CCGTTTTCTTGGATC	90678
rs780372521	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127489678	GAACCTCCCTTTGCT[C/T]CCAGCCTTGTGTCGG	90678
rs780466674	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127501785	ACTTACTCTAAAAAT[C/T]ACACAGAGCAGTGAA	90678
rs780492552	snp	A/C	2.32788e-05	0.00341158	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127502858	TGCCCGCTGTGCCGC[A/C]AGGACATCGCCCAGC	90678
rs780515350	snp	C/T	1.64741e-05	0.00286998	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127462367	GGCTCACGTTCGAAC[C/T]CTGGAGGTAAATGGG	90678
rs780523082	snp	G/T	4.99197e-05	0.00499573	intron-variant	LRSAM1	GRCh38.p7	9:127481154	GGCCTGCTGGTGACT[G/T]CCAGGACCTTTTATG	90678
rs780555907	snp	A/G	1.73234e-05	0.00294302	intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451252	GGGATGCTCCATCCC[A/G]CAGCCCCGGCCACAA	90678
rs780563846	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127455784	GATAGGAGAGTAGGC[C/T]TTGGGGTTGGACCTT	90678
rs780574219	snp	C/T			upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	RPL12, LRSAM1	GRCh38.p7	9:127452031	AGTGATCGGCCTGCC[C/T]TCGGGTGCACCCGCG	90678
rs780605033	snp	C/T	3.41134e-05	0.00412983	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127479896	CACCTCAACGCAGAG[C/T]GGCAGCGGCTGCAGG	90678
rs780631664	snp	A/C/G			intron-variant	LRSAM1	GRCh38.p7	9:127483104	CCCTCTGTTGGCCAT[A/C/G]CATGGAGGGCCCTGA	90678
rs780636250	snp	A/G	4.84825e-05	0.0049233	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127467755	ATGCTGAGCCTTGAC[A/G]CCTCGGCCATGGTCT	90678
rs780678364	snp	A/G	4.12856e-05	0.00454325	intron-variant	LRSAM1	GRCh38.p7	9:127492757	CTGCGGGACTCCTGC[A/G]CTGCCGCCAGCTCAC	90678
rs780857041	snp	A/T			intron-variant	LRSAM1	GRCh38.p7	9:127484756	TGTGTGTGTACAAAC[A/T]TCTATTCTAGTTCCT	90678
rs780868977	snp	A/G	1.65165e-05	0.00287367	intron-variant	LRSAM1	GRCh38.p7	9:127479983	GACAATCAGAGGTTG[A/G]GCTCTGCTCCTCGGC	90678
rs780899337	in-del	-/T			intron-variant	LRSAM1	GRCh38.p7	9:127499538	CTGTCTAAAAAAAAA[-/T]TATATATATATATAT	90678
rs780919204	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127495742	CCCCTCTTGGTGGAT[A/G]TTCAAGTTGCTTACT	90678
rs780947115	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127483348	GCGCTTTAGGAAGCC[A/G]AGGCTGGAGGATCAC	90678
rs780956904	snp	C/T	0.000281992	0.0118708	synonymous-codon, intron-variant, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127491245	ACTGAGTTATTGCAG[C/T]TGACACAGCTGGAGT	90678
rs780990825	snp	C/G	0.000198	0.00994791	intron-variant	LRSAM1	GRCh38.p7	9:127473956	GGCAGCCTGCTGCAC[C/G]CATACATGTGTGTGT	90678
rs781011389	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127476464	AAGGTGGGAGGATGG[C/T]TTAAGCCCAGGAGGT	90678
rs781022270	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127496715	TCCACCCCAAGCAGT[A/G]TGGCCCCAGAGTTCG	90678
rs781037777	in-del	-/A			intron-variant	LRSAM1	GRCh38.p7	9:127467103	TAGCTGGCAACCGAG[-/A]GGCAGCTAATGCTCA	90678
rs781084277	in-del	-/A	1.64743e-05	0.00287	frameshift-variant, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127461230	TCCATTGGGAACCTG[-/A]CCCAGCTCCAGACTC	90678
rs781097238	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127490236	TTGCATGGTTTTTTT[C/T]TTTCTCTATTTTTCT	90678
rs781207483	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127462537	AATGTGTGAACATTC[A/G]TAATTATATGACTTT	90678
rs781209296	snp	C/G	1.65321e-05	0.00287502	missense, intron-variant, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127495388	GTATCAACGGCTTTT[C/G]AACCAGAAGCCCTTG	90678
rs781213154	snp	G/T	2.73594e-05	0.00369851	intron-variant	LRSAM1	GRCh38.p7	9:127483070	GCCTGCTGGCTGGGC[G/T]GGCAGGGTGGATGGC	90678
rs781236745	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127491834	GGATGCCTGGGAGCC[A/G]GGTGTGGCCCAGCAC	90678
rs781265596	snp	C/T	8.37542e-05	0.00647071	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127454570	CCCAGTGAGGAGGCT[C/T]GGAAACGCCTGGAGT	90678
rs781299210	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127461467	TGTGGCTCCTGAGAG[C/T]CAGGGCCGTATGGCC	90678
rs781381373	snp	C/T	3.30055e-05	0.00406222	intron-variant	LRSAM1	GRCh38.p7	9:127454973	TTTTGTCTTAATACT[C/T]TTTAAAAATTCTTTT	90678
rs781399543	in-del	-/CAA			intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127450103	AGTAATCCTTAGCCT[-/CAA]CAGGAGGCTAAGTGT	90678
rs781472087	snp	G/T			intron-variant	LRSAM1	GRCh38.p7	9:127499610	TGATAGCCTTAGAGG[G/T]TCTAGTGTTGTAACA	90678
rs781511247	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127489244	GTGCGATGCCGGAAG[C/T]GCATCAGGTAGAGGC	90678
rs781577020	snp	C/T	3.29674e-05	0.00405988	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127462280	GGAGCTTCCAGACAC[C/T]GTGGGGGAGCTTCGA	90678
rs781586877	in-del	-/CAAA			intron-variant	LRSAM1	GRCh38.p7	9:127475497	AGACTCCATCTCAAA[-/CAAA]CAAACAAACAAACAA	90678
rs781598793	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127474538	AGTTCCTTGGTAGCA[C/G]TTATCACAGCGCTAA	90678
rs781610879	snp	C/G	1.71634e-05	0.0029294	intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127449753	TGTCCAGAGGTGAAC[C/G]ACAGCCTTGAAACCT	90678
rs781611387	snp	A/G	5.7012e-05	0.0053388	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127487757	CATCAGCCAGATCCT[A/G]CAGGAGGTGAGCCCT	90678
rs781650130	snp	C/T	1.7348e-05	0.00294512	intron-variant	LRSAM1	GRCh38.p7	9:127479792	CAGTACCCCTCACGG[C/T]GTCTGAGGGGGTCCC	90678
rs781680086	snp	A/G	1.6549e-05	0.0028765	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127457329	AGGTGCTGATCGTCC[A/G]CACGAATCACCTCAC	90678
rs781702646	snp	C/T	6.61967e-05	0.00575273	intron-variant	LRSAM1	GRCh38.p7	9:127489412	AAAGTGTGGGCACGG[C/T]CCCTGCTGAGGGCTG	90678
rs781739526	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127480955	AAGTGCTGGGATTAC[A/G]GATGTGAGCCACTGT	90678
rs786200930	in-del	-/GC			frameshift-variant, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127502849	TGCGCACCTGCCCGC[-/GC]TGTGCCGCCAGGACA	90678
rs796082039	snp	A/C			intron-variant	LRSAM1	GRCh38.p7	9:127467095	TCCTTTATTAGCTGG[A/C]AACCGAGAGGCAGCT	90678
rs796101393	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127467486	AAGAAACTAAAATGG[A/G]GTCTGTCCGGCTCTC	90678
rs796101610	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127467491	ACTAAAATGGAGTCT[C/G]TCCGGCTCTCTCTCT	90678
rs796122937	snp	A/G/T			intron-variant	LRSAM1	GRCh38.p7	9:127467453	CCTTAAGGGAGGGAG[A/G/T]GAAGGGGGCTGCAGG	90678
rs796128022	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127467134	AAATTCTCTTGGCCC[C/T]GAGGAAGGGGCTAGT	90678
rs796164112	snp	G/T			intron-variant	LRSAM1	GRCh38.p7	9:127467468	GGAAGGGGGCTGCAG[G/T]TGAAGAAACTAAAAT	90678
rs796207918	snp	A/G			intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127449879	GGGGTTGGGGTTCTT[A/G]TCCAGAACTGTAAAC	90678
rs796235280	in-del	AACAAAAC/CAA			intron-variant	LRSAM1	GRCh38.p7	9:127458412	ACAAAACAAAACAAA[AACAAAAC/CAA]AAAAAAAACACCAGC	90678
rs796240869	in-del	-/T			intron-variant	LRSAM1	GRCh38.p7	9:127488599	TTTTCTTTTCTTTTC[-/T]TTTTTTTTTTTTTAA	90678
rs796275019	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127467054	GAGTTATAGAGAAAC[A/G]CCACACTTTGAGACA	90678
rs796292251	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127467082	ACAAATTGAGGAGTC[C/T]TTTATTAGCTGGCAA	90678
rs796303231	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127467096	CCTTTATTAGCTGGC[A/G]ACCGAGAGGCAGCTA	90678
rs796377682	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127467074	ACTTTGAGACAAATT[A/G]AGGAGTCCTTTATTA	90678
rs796399867	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127460847	TCTTCCTGTTTCTTT[C/T]TTTTTTTTTTTTTTT	90678
rs796426336	in-del	-/CA			intron-variant	LRSAM1	GRCh38.p7	9:127463198	AGCAAGACTTTGTCT[-/CA]AAAAAAAAAAAAAAA	90678
rs796478456	snp	G/T			upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	RPL12, LRSAM1	GRCh38.p7	9:127451545	GCTGACGGCTGGCAA[G/T]CAGGGCACCGCGGTG	90678
rs796502443	in-del	-/C			intron-variant	LRSAM1	GRCh38.p7	9:127458394	ACTTCGTCTCAAAAA[-/C]AAAACAAAACAAAAC	90678
rs796671295	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127467457	AAGGGAGGGAGGGAA[A/G]GGGGCTGCAGGTGAA	90678
rs796744270	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127467506	GTCCGGCTCTCTCTC[C/T]GCTAGGAGAGAGTCA	90678
rs796778718	snp	A/C			intron-variant	LRSAM1	GRCh38.p7	9:127480164	GACCCAGTCATTACA[A/C]AGTCTGGTTTCTTAG	90678
rs796804839	in-del	CTT/TC			intron-variant	LRSAM1	GRCh38.p7	9:127484809	GATTTTTCTTTTTTT[CTT/TC]TTTTTTTTTTTTTTT	90678
rs796845940	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127467507	TCCGGCTCTCTCTCT[A/G]CTAGGAGAGAGTCAC	90678
rs796949550	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127467113	CCGAGAGGCAGCTAA[C/T]GCTCAAAATTCTCTT	90678
rs796978404	in-del	AG/T			intron-variant	LRSAM1	GRCh38.p7	9:127500154	CACCTGAAGTCAAAA[AG/T]TTGAGACCAGCCTGG	90678
rs796982514	in-del	-/T			intron-variant	LRSAM1	GRCh38.p7	9:127467456	AAGGGAGGGAGGGAA[-/T]GGGGGCTGCAGGTGA	90678
rs796992042	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127467092	GAGTCCTTTATTAGC[C/T]GGCAACCGAGAGGCA	90678
rs797044913	snp	C/T			missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127502847	CACTGCGCACCTGCC[C/T]GCTGTGCCGCCAGGA	90678

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