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

LYN

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs112784952	snp	A/T	0.0228947	0.104514	intron-variant	LYN	GRCh38.p7	8:55985944	GGCTGAGGCAGGAGG[A/T]TCAGTTGAACCCAGG	4067
rs112812049	snp	G/T	0.5	0	intron-variant	LYN	GRCh38.p7	8:56003933	ATATTTTATTCTTTT[G/T]TTTTTTTTTTTTTTT	4067
rs112844004	snp	A/G	0.0414363	0.137845	intron-variant	LYN	GRCh38.p7	8:56000781	TCCCAGAGCCTTCAT[A/G]TTTTCATTTATGTTT	4067
rs112948393	snp	A/G	0.5	0	intron-variant	LYN	GRCh38.p7	8:55966424	CCAGGCTGGAATGCA[A/G]TGGTGCGATCTCAGC	4067
rs112955833	snp	A/G	0.5	0	intron-variant	LYN	GRCh38.p7	8:55936950	CCAGGGACAAAGTAG[A/G]CACATACGTGTTTAT	4067
rs112991976	in-del	-/A	0.151001	0.229563	intron-variant	LYN	GRCh38.p7	8:55927843	TCTGTCCCAAGGGGG[-/A]AAAAAAAAAGAAAGA	4067
rs112993878	snp	A/G	0.0189856	0.0955633	intron-variant	LYN	GRCh38.p7	8:55972321	TCAGACTCTTTCCCA[A/G]CCCTTCCCTCAAGGT	4067
rs112997254	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55880605	GAGATGGGGCTCGGC[C/T]GGCGCCCTCTCGAGG	4067
rs113000587	snp	G/T	0.5	0	intron-variant	LYN	GRCh38.p7	8:55976676	GGAGGATGGAGCGTA[G/T]TAGGGTGGGCTAGCA	4067
rs113010746	snp	A/G	0.00716266	0.059414	intron-variant	LYN	GRCh38.p7	8:55930738	CAGCATGTTGATGGG[A/G]GACCAAGACCTGGTC	4067
rs113026375	snp	C/T	0.0134861	0.0810011	intron-variant	LYN	GRCh38.p7	8:55903487	AAAAAACTACTTGAG[C/T]GTTTTTGATTACCAA	4067
rs113033827	snp	A/G	0.00755907	0.0610114	intron-variant	LYN	GRCh38.p7	8:55910100	ATTCTGCAGGTTGTC[A/G]GTTCATTCCTGTTGA	4067
rs113034219	snp	A/G	0.00676609	0.0577691	intron-variant	LYN	GRCh38.p7	8:55904392	ACTGAACACCAGCAA[A/G]TGTATTTACAATCCT	4067
rs113051495	snp	A/G	0.0232847	0.105357	intron-variant	LYN	GRCh38.p7	8:55964302	CTCCTGGGCTCAAGC[A/G]ATCCTCCTGCCTCTC	4067
rs113086332	in-del	-/CA	0.0520825	0.152737	intron-variant	LYN	GRCh38.p7	8:56003220	GCCCGCCACCACGCC[-/CA]GCTAATTTTTTTTTT	4067
rs113090201	snp	A/G	0.5	0	intron-variant	LYN	GRCh38.p7	8:55882521	CATGCCCACAGCAGG[A/G]AACATTGTTATAAGC	4067
rs113093211	snp	C/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55889992	ATCAAAAGCAAGTTG[C/G]TTAGCTGGGTGAAGT	4067
rs113126729	snp	G/T	0.0232847	0.105357	intron-variant	LYN	GRCh38.p7	8:55965102	GGAAGAGTATGATTA[G/T]TAATATTTCTGCTTT	4067
rs113148560	snp	G/T	0.5	0	intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55922432	ATGTGTGCCAGTGTA[G/T]TAATTTATCTAATCA	4067
rs113163883	snp	A/G	0.00755907	0.0610114	intron-variant	LYN	GRCh38.p7	8:55912502	GGTCGAGGCAAGCGG[A/G]TCACCTGAGGTCCAG	4067
rs113169087	snp	A/G	0.00318978	0.0398085	intron-variant	LYN	GRCh38.p7	8:55933231	ATCTAATATGACATT[A/G]CGTAAATCTGAAATA	4067
rs113196835	in-del	-/A	0.174932	0.238463	intron-variant	LYN	GRCh38.p7	8:55935210	TTAGGTTGCCTAAAG[-/A]AAAAAAAACAAAAAC	4067
rs113217710	snp	A/G	0	0	intron-variant	LYN	GRCh38.p7	8:55950904	GGTAGTAAAAGTTTT[A/G]TGGTTTGATAACAAA	4067
rs113224256	in-del	-/A	0.5	0	downstream-variant-500B	LYN	GRCh38.p7	8:56012727	GTGAGACCCTGTCTC[-/A]AAAAAAAAAACCAAA	4067
rs113236644	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55997944	AAAAAATTAGCCGGG[A/C]ATGGTGGTGGGTGCC	4067
rs113240911	snp	C/G	0	0	intron-variant	LYN	GRCh38.p7	8:55887879	CCTCCCGAAATCCGG[C/G]GATTACAGGCATAAG	4067
rs113242972	snp	A/T	0.00517822	0.0506191	intron-variant	LYN	GRCh38.p7	8:55938315	GCCTCAGTTACTATC[A/T]TGTTTTAACCAAATT	4067
rs113292614	snp	C/T	0.0463947	0.145069	intron-variant	LYN	GRCh38.p7	8:55966587	TAGCCAGGCTGGTTT[C/T]GAACTCCTGACATCA	4067
rs113296227	snp	A/T	0.5	0	intron-variant	LYN	GRCh38.p7	8:56000168	ACAGGGGCTCCTCCA[A/T]GGCAGTCCCCCTGAC	4067
rs113325751	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55952181	GTATAAGACGTCAAA[C/T]GCTATTTTTATATTA	4067
rs113334442	snp	G/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55940183	CCTTCCCCAAACTCC[G/T]GTCATCTCTCCTTCC	4067
rs113354539	in-del	-/AAAT	0.5	0	intron-variant	LYN	GRCh38.p7	8:55954835	TGAGACCCTGCCTCA[-/AAAT]AAATAAATAAATAAA	4067
rs113359223	snp	A/G	0.00835141	0.0640778	intron-variant	LYN	GRCh38.p7	8:55903083	CGAACTCCTGACTTC[A/G]CGATCCGCCCACTTC	4067
rs113383457	snp	A/G	0.000693035	0.0186021	intron-variant	LYN	GRCh38.p7	8:55947594	GATGGATTCTTACAG[A/G]TGTTCTCTTGTGTTC	4067
rs113395642	snp	C/T	0.155987	0.23165	intron-variant	LYN	GRCh38.p7	8:55894555	TTTTTTTTTTTTTGA[C/T]GGAGTCTTGTTCTGT	4067
rs113437785	in-del	-/C	0.354235	0.227234	intron-variant	LYN	GRCh38.p7	8:55933886	TGGATAACTAGATGA[-/C]CCCTGGGTCTACCTA	4067
rs113473857	snp	C/T	0.00795532	0.062565	intron-variant	LYN	GRCh38.p7	8:55882831	ACAGGCTTGGTTAAG[C/T]GGTACCATTAGGAGT	4067
rs113498934	snp	A/C	0.5	0	intron-variant, missense	LYN	GRCh38.p7	8:55941938	CAACCAGTACGTAAT[A/C]CTGAAAGAACTATTT	4067
rs113515656	snp	A/C	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55919117	ACCAGGAGATAACAC[A/C]TTTTAAGCAGAAATA	4067
rs113516956	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55945257	TAAGGGCTTTTTGAA[A/G]TTTGAAAAATCAGCT	4067
rs113518475	snp	A/G	0.0182019	0.0936463	intron-variant	LYN	GRCh38.p7	8:55969548	GGTAACAGATTAGAG[A/G]GGACTGCGTTTGACC	4067
rs113548964	snp	A/G	0.5	0	intron-variant	LYN	GRCh38.p7	8:55999323	GAAACTCCGCCTCAA[A/G]AAAAGAAAAGAAAAG	4067
rs113680819	in-del	-/TTTG/TTTTTG	0.478603	0.101197	intron-variant	LYN	GRCh38.p7	8:55932413	ATTATATATATATTT[-/TTTG/TTTTTG]TTTGTTTGTTTGTTT	4067
rs113732653	snp	A/C	0.0441095	0.141807	intron-variant	LYN	GRCh38.p7	8:55973433	TGCTTTTTGTGCTGA[A/C]ATAGGAAAATACCTC	4067
rs113767209	snp	A/G	0.5	0	intron-variant	LYN	GRCh38.p7	8:55917188	CTAAAAAAAAAAAAA[A/G]AGAGAGAGAGAGAGA	4067
rs113780740	snp	C/T	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:55898925	GATCTTCTGGGCTCA[C/T]GCAATCCTCCTGCCT	4067
rs113797373	snp	A/G	0.00597247	0.0543191	intron-variant	LYN	GRCh38.p7	8:55909432	GACTTGGACATGTTC[A/G]GTCATAATCCCACAG	4067
rs113803306	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55953727	TTAGTTCACAGACTG[C/T]GGCAGGTTGGACACT	4067
rs113809677	snp	A/G	0.5	0	intron-variant	LYN	GRCh38.p7	8:55903584	AAATCATTTCCTGGA[A/G]GGATATTTTTCACTG	4067
rs113823687	in-del	-/G	0.210909	0.246925	intron-variant	LYN	GRCh38.p7	8:55956119	TGCTCATTAAAAAAA[-/G]AATGACTTGGCTTCT	4067
rs113830662	snp	A/C	0.0441095	0.141807	intron-variant	LYN	GRCh38.p7	8:55970311	ACTATTTTTAGTACT[A/C]GCCTAGGAGTTGCCT	4067
rs113831648	snp	C/G	0.5	0	intron-variant	LYN	GRCh38.p7	8:55934468	ATATTCTGTGTATGC[C/G]GTTCACCGGCCCGCT	4067
rs113836139	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55997943	CAAAAAATTAGCCGG[G/T]CATGGTGGTGGGTGC	4067
rs113852290	snp	C/T	0.0256215	0.110247	intron-variant	LYN	GRCh38.p7	8:55979260	TTGGCCAGGCTGGTC[C/T]TGAACTCCCAACCTC	4067
rs113864571	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55985053	GTGGGCTTCAATAGT[C/T]GGGAAACACTGCCAT	4067
rs113879359	snp	C/T	0.0763149	0.179815	intron-variant	LYN	GRCh38.p7	8:55951076	AGCAAGACCCCATCT[C/T]TACAAGAAATACAAA	4067
rs113882944	snp	C/G	0	0	intron-variant	LYN	GRCh38.p7	8:55909989	TGTGTGTGTGTGTGT[C/G]TGTCTTTTTTTTTTT	4067
rs113888818	in-del	-/A	0	0	intron-variant	LYN	GRCh38.p7	8:55891352	GCGAAACTCCGGCTC[-/A]AAAAAAAAAAAAAAG	4067
rs113898051	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55970524	TCAGTATTGGCAATC[A/G]GTGGTTTCATGAAGC	4067
rs113907647	snp	C/T	0.00636936	0.0560724	intron-variant	LYN	GRCh38.p7	8:55950041	GTGGTCCTTTTTGAC[C/T]GCCTTCTTTTATTTA	4067
rs113911134	snp	A/G	0.5	0	intron-variant	LYN	GRCh38.p7	8:55934733	TCCTGTGTTGAGGGG[A/G]GTGCACCCTGTAACT	4067
rs113913959	snp	A/G	0.00318978	0.0398085	intron-variant	LYN	GRCh38.p7	8:55915228	CTTCCATATTCCAAC[A/G]CATAAGGTTCTTTGC	4067
rs113929937	snp	A/G	0.029116	0.117091	intron-variant	LYN	GRCh38.p7	8:55966461	CAACCTCCACCTCCT[A/G]GGTTCAAGCAATTCT	4067
rs113953388	snp	A/G	0.0799831	0.183287	intron-variant	LYN	GRCh38.p7	8:55937770	CAACAATCTTGGCTT[A/G]CTGCAACCTCTGCCT	4067
rs113967772	snp	A/G	0.144296	0.226554	intron-variant	LYN	GRCh38.p7	8:55905392	CCAGCCTGGGCAACA[A/G]GAGTGAAACTCCGTC	4067
rs113999671	snp	A/C	0.00874735	0.0655527	utr-variant-5-prime	LYN	GRCh38.p7	8:55877806	TGCCTCTGATCACTG[A/C]CTTCTGTGCTCAATT	4067
rs114056291	snp	C/T	0.00358779	0.0422022	intron-variant	LYN	GRCh38.p7	8:55890770	TTTTACTCTGTCACC[C/T]GGGCTAGAGTGTGGT	4067
rs114057898	snp	C/T	0.0178098	0.0926698	intron-variant	LYN	GRCh38.p7	8:55983741	TGCTTTTCCTTCCCC[C/T]TCACCAGCCAGCTTC	4067
rs114064602	snp	C/G	0.0142736	0.0832652	intron-variant	LYN	GRCh38.p7	8:56005138	AAGCTGAAAGGTCCC[C/G]CACTCTATTCCCAGC	4067
rs114077541	snp	C/T	0.00318978	0.0398085	intron-variant	LYN	GRCh38.p7	8:55892770	AATTTTTTAAAAAGT[C/T]TTCCCAATGCAGGAG	4067
rs114077690	snp	A/G	0.128632	0.218563	intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55923564	TTTTTTTTTGAGACA[A/G]GGTCTTGCTCTGTCC	4067
rs114084212	snp	C/T	0.0217236	0.101931	intron-variant	LYN	GRCh38.p7	8:55995783	GGGCTGAGCCGGGGC[C/T]GGGTCATACGGGGCC	4067
rs114123387	snp	A/G	0.0349115	0.127424	intron-variant	LYN	GRCh38.p7	8:55898802	TCTATTTCTAGCTCT[A/G]TAATAAATTTTAGGA	4067
rs114230961	snp	C/T	0.0279526	0.114869	intron-variant	LYN	GRCh38.p7	8:55884210	GTTCAAGCAATCCTC[C/T]CTGCCTCAGCCTTCT	4067
rs114267736	snp	C/T	0.0275645	0.114116	intron-variant	LYN	GRCh38.p7	8:55885472	AGCTTCTTTCCAGTC[C/T]CCGCTTTCCTCCCTC	4067
rs114309789	snp	C/T	0.0263992	0.111815	intron-variant	LYN	GRCh38.p7	8:55980942	CCAGCTCCCCGCGGC[C/T]GCTTGCTAGCCCCTG	4067
rs114324822	snp	C/T	0.0248432	0.108648	intron-variant	LYN	GRCh38.p7	8:55945937	GGGTCCCACCTCTTC[C/T]GTCTCCATCCTGCTG	4067
rs114337099	snp	A/T	0.0168055	0.0901129	intron-variant	LYN	GRCh38.p7	8:55991364	CCTCAAAGCCCTGAC[A/T]TATGGAAGGCATCTG	4067
rs114411338	snp	C/T	0.0429648	0.14013	intron-variant	LYN	GRCh38.p7	8:55964308	GGCTCAAGCGATCCT[C/T]CTGCCTCTCAAAGTG	4067
rs114496048	snp	A/C	0.0150606	0.0854603	intron-variant	LYN	GRCh38.p7	8:56005486	ATGGTATATGCTGAC[A/C]ACACAGTGTGTGCCT	4067
rs114641977	snp	A/G	0.00835141	0.0640778	intron-variant	LYN	GRCh38.p7	8:55885838	ACTTCCTCCACCCCA[A/G]GCCCCTGGGTCATTT	4067
rs114645370	snp	C/T	0.0221141	0.102801	intron-variant	LYN	GRCh38.p7	8:55901620	GGGGTCAGGTAGGGC[C/T]GGGGGAGGTCCTGCA	4067
rs114645669	snp	A/G	0.0168055	0.0901129	intron-variant	LYN	GRCh38.p7	8:55921585	TGGGTTTTGAGTTAC[A/G]TTTGGAAGACAGGTG	4067
rs114663752	snp	A/G	0.0182019	0.0936463	intron-variant	LYN	GRCh38.p7	8:55970425	AAATATCAAGGAAAT[A/G]CACACTTGAATGATG	4067
rs114676605	snp	A/G	0.0185938	0.0946107	intron-variant	LYN	GRCh38.p7	8:55933878	TTCACATTGTGGATA[A/G]CTAGATGACCCTGGG	4067
rs114723617	snp	C/T	0.00755907	0.0610114	intron-variant	LYN	GRCh38.p7	8:55907519	ATCTACCAGAACTGA[C/T]GTCAGCACAGTTAGG	4067
rs114758246	snp	A/C	0.00318978	0.0398085	intron-variant	LYN	GRCh38.p7	8:55889019	TGTATTTCTTTCTTT[A/C]TTTATTTGTATGTTT	4067
rs114938418	snp	A/G	0.00835141	0.0640778	intron-variant	LYN	GRCh38.p7	8:55964255	TGTTTTAGAGAAGGG[A/G]GTCTCACTATATTGC	4067
rs114953482	snp	G/T	0.0142736	0.0832652	intron-variant	LYN	GRCh38.p7	8:56009284	TATTAAAGAGAACTT[G/T]GCTGTGGCTCCTACT	4067
rs115052227	snp	C/T	0.0228947	0.104514	intron-variant	LYN	GRCh38.p7	8:55883009	AATACACTTAACCTA[C/T]TAAACATTATAGATT	4067
rs115163019	snp	A/C	0.262985	0.249663	utr-variant-3-prime	LYN	GRCh38.p7	8:56010731	CTGCTCAGACCTGCT[A/C]GACATGCCATAGGAG	4067
rs115218765	snp	A/C	0.0410537	0.137264	downstream-variant-500B	LYN	GRCh38.p7	8:56012737	AAAAAACCAAAAAAA[A/C]AAAAAAACCCTTCCC	4067
rs115229674	snp	C/T	0.198014	0.244535	intron-variant	LYN	GRCh38.p7	8:55936977	TTATCCCTTTTCTAC[C/T]CCCCACGTCTTTTGT	4067
rs115268144	snp	A/G	0.00716266	0.059414	intron-variant	LYN	GRCh38.p7	8:55928447	CACCACGCAGGGCCC[A/G]TTGTTGCTTTAATTT	4067
rs115374032	snp	C/T	0.00438332	0.0466095	intron-variant	LYN	GRCh38.p7	8:55956013	ATGTGGACACATTTT[C/T]ATTTCTCTTGTGTAT	4067
rs115432715	snp	A/G	0.00676609	0.0577691	intron-variant	LYN	GRCh38.p7	8:55987311	TACTGGGGAGGCTGA[A/G]GCACAAGAATTGCTC	4067
rs115525198	snp	C/T	0.0142736	0.0832652	intron-variant	LYN	GRCh38.p7	8:56003623	GAAGTTGCAGTGAGC[C/T]GAGATGCGCCACTGC	4067
rs115531140	snp	G/T	0.00318978	0.0398085	intron-variant	LYN	GRCh38.p7	8:55928839	TGTTGTATGTAAAAT[G/T]TCATCACCAAACCCA	4067
rs115533771	snp	C/T	0.00716266	0.059414	intron-variant	LYN	GRCh38.p7	8:55902399	GTGGCGTGAATTCAG[C/T]TCACTGCAACTTCCG	4067
rs115577614	snp	G/T	0.030278	0.119257	intron-variant	LYN	GRCh38.p7	8:55956774	CTTCCCGGCTTCTCC[G/T]TCTGTTCACTGAGAG	4067
rs115595045	snp	G/T	0.00597247	0.0543191	intron-variant	LYN	GRCh38.p7	8:55898204	TTGTCTGTCCCCATT[G/T]TTTTGTGTTTTCTGT	4067
rs115595170	snp	A/C/G	0.00398564	0.0444627	intron-variant	LYN	GRCh38.p7	8:55881897	GTAGGTGCTCAGTTC[A/C/G]AGATTACTTGGAAGA	4067
rs115725725	snp	G/T	0.107341	0.205301	intron-variant	LYN	GRCh38.p7	8:55921078	GGGGGACATTTTGTT[G/T]GTTTTCATCGTCTAG	4067
rs115727626	snp	C/T	0.00795532	0.062565	intron-variant	LYN	GRCh38.p7	8:55890329	AAATAATAATAACAA[C/T]AATAAAAAGAAAGTT	4067
rs115732983	snp	C/T	0.0879971	0.190408	intron-variant	LYN	GRCh38.p7	8:55898962	CCTGTGTAGCTGGGA[C/T]CACAGGTGTACACCA	4067
rs115736213	snp	A/G	0.00914312	0.0669923	intron-variant	LYN	GRCh38.p7	8:55938082	AATCACTCTTCTAAT[A/G]TTCTAAGGCTCTTGA	4067
rs115737585	snp	A/G	0.0383715	0.133092	intron-variant	LYN	GRCh38.p7	8:55972070	TACCAAATCCAGCCC[A/G]TGCCAGGTGAACTCA	4067
rs115741345	snp	C/T	0.0314385	0.121371	intron-variant	LYN	GRCh38.p7	8:55976512	CAGCTATCCTGAGCA[C/T]AGCCAGGCACTGTGT	4067
rs115760560	snp	C/T	0.0119091	0.0762411	intron-variant	LYN	GRCh38.p7	8:55984716	GCAGTCAGAGCAATG[C/T]TTTGAGGCATAAATC	4067
rs115786610	snp	C/T	0.151334	0.229706	intron-variant	LYN	GRCh38.p7	8:55883529	TGCTGTCCGAGCAGC[C/T]CTAGTGACTGTCTTG	4067
rs115891639	snp	C/T	0.0142736	0.0832652	intron-variant	LYN	GRCh38.p7	8:56007180	AGGAAGTGAAAGAGA[C/T]ATTCCAAACTGAGTG	4067
rs115897175	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	LYN	GRCh38.p7	8:56012138	CTTCACCAGCTTGGG[C/T]CTCATCTCTGGTGTC	4067
rs115904008	snp	A/G	0.0228947	0.104514	intron-variant	LYN	GRCh38.p7	8:55883205	TACAGTTTTTATTGA[A/G]TGCCTAATGCTTTTG	4067
rs115906207	snp	A/G	0.0130921	0.0798413	intron-variant	LYN	GRCh38.p7	8:55914694	CTTTTCATCAGCCTC[A/G]CTCACCTTACCCTTC	4067
rs115943078	snp	G/T	0.0221141	0.102801	intron-variant	LYN	GRCh38.p7	8:55939786	GAGGGTGACGGGGCG[G/T]GGGAGGGATGAGACT	4067
rs115951309	snp	A/G	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55953168	GCCTGGGGTCCAGTG[A/G]TGACATGACCGAGTC	4067
rs115960443	snp	C/T	0.106633	0.204807	intron-variant	LYN	GRCh38.p7	8:55905335	AGAATTACTTCAACC[C/T]GGGAGGTGGAGATTG	4067
rs115961824	snp	A/G	0.00150855	0.0274226	intron-variant	LYN	GRCh38.p7	8:55950825	TAAAACACTATTTAG[A/G]AAATTATTTTTAGAA	4067
rs115976578	snp	A/G	0.0115144	0.0749975	intron-variant	LYN	GRCh38.p7	8:55931815	CTCAAATGTTACACC[A/G]TACCAGAAGACTTGT	4067
rs116009022	snp	C/T	0.0103295	0.0711199	intron-variant	LYN	GRCh38.p7	8:55964966	GCTATCCAGCTTTTG[C/T]GCACCAGGCAGCAGG	4067
rs116014989	snp	C/G	0.0263992	0.111815	intron-variant	LYN	GRCh38.p7	8:55889851	GCTGGCAAGGTGCTG[C/G]CCTTGCTAGCCTCAG	4067
rs116070406	snp	C/T	0.00993419	0.0697739	intron-variant	LYN	GRCh38.p7	8:55912414	GCGCTTAAGTAGTTT[C/T]TGAAATTTTAACCCA	4067
rs116188338	snp	C/G	0.132066	0.220435	intron-variant	LYN	GRCh38.p7	8:55882589	TGTTAACATTGAAAG[C/G]CCACCACAATCATTA	4067
rs116229128	snp	A/G	0.0349115	0.127424	intron-variant	LYN	GRCh38.p7	8:55949802	ACAATCCATCTACTT[A/G]AAGTGTACAATTCAG	4067
rs116230911	snp	A/G	0.00914312	0.0669923	intron-variant	LYN	GRCh38.p7	8:55987274	AAAAATTAGCTGAGT[A/G]TGGTGGCGAGTAGGT	4067
rs116250570	snp	A/G	0.00835141	0.0640778	intron-variant	LYN	GRCh38.p7	8:55911561	AGCAGGTGGAAATGT[A/G]CATTCACTACTTGGT	4067
rs116330933	snp	A/T	0.0138799	0.0821421	intron-variant	LYN	GRCh38.p7	8:55885431	TGCTCACTCCTCTTT[A/T]TTGACACCAGACCAT	4067
rs116347210	snp	A/G	0.039522	0.134904	intron-variant	LYN	GRCh38.p7	8:56003526	AAAAAAAATTAGCCC[A/G]GCGTGGTGGCCAACG	4067
rs116360722	snp	C/G	0.0345262	0.126772	intron-variant	LYN	GRCh38.p7	8:55898947	CTCCTGCCTCAGCCT[C/G]CTGTGTAGCTGGGAC	4067
rs116409837	snp	A/G	0.0228947	0.104514	intron-variant	LYN	GRCh38.p7	8:55883401	TGCACCATCAAGCTG[A/G]GCACTTCAAGCTGTC	4067
rs116411256	snp	A/G	0.029116	0.117091	intron-variant	LYN	GRCh38.p7	8:55951020	GGCTGAGGCGAGAGG[A/G]TCACTTGAGTCCAGC	4067
rs116437271	snp	A/C	0.00795532	0.062565	intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55923858	TCAAACAACTTAATA[A/C]ATGTTTGTTATAATG	4067
rs116533510	snp	A/G	0.0707826	0.174302	intron-variant	LYN	GRCh38.p7	8:55939586	CACAGCTCAGTCAGG[A/G]CTCGGTCCGTGCTGG	4067
rs116545958	snp	A/G	0.0189856	0.0955633	intron-variant	LYN	GRCh38.p7	8:55978535	GGGCTAGAGGCTTCA[A/G]GGAGGCTGGTGCTGC	4067
rs116558247	snp	C/T	0.0279526	0.114869	intron-variant	LYN	GRCh38.p7	8:55884908	TACTGAATTAGCTGG[C/T]AGCATTCCTTATTTG	4067
rs116597435	snp	C/T	0.00318978	0.0398085	intron-variant	LYN	GRCh38.p7	8:55945641	CCCAGAGGCCTCACA[C/T]AGCCTCATGTGGCAC	4067
rs116636440	snp	A/G	0.00438332	0.0466095	intron-variant	LYN	GRCh38.p7	8:55905732	CCTCACTCCTCTCCC[A/G]TCTGTTGGGAGAGCC	4067
rs116669620	snp	A/T	0.00318978	0.0398085	intron-variant	LYN	GRCh38.p7	8:55896526	GGGGGCCTAAGGGAG[A/T]GATGGCATTAGGAGA	4067
rs116670765	snp	A/G	0.0174175	0.0916809	intron-variant	LYN	GRCh38.p7	8:55899497	ATAAGACCACTTCTG[A/G]GAAATGTATAATAAA	4067
rs116720656	snp	A/G	0.0209421	0.100162	intron-variant	LYN	GRCh38.p7	8:55977389	GTGGATGCTTTTTGT[A/G]TTTACTGTAATATGT	4067
rs116729826	snp	C/T	0.0166325	0.0896639	intron-variant	LYN	GRCh38.p7	8:55887023	TCCAACGTACAGAGA[C/T]GGGCAGTCCAATAGG	4067
rs116750101	snp	C/T	0.00716266	0.059414	intron-variant	LYN	GRCh38.p7	8:55901448	ATCTCAAGGCCAGGC[C/T]TTAGACTCCTTCTTG	4067
rs116835537	snp	G/T	0.00557542	0.0525036	intron-variant	LYN	GRCh38.p7	8:55894019	GAAGAACATGCACAG[G/T]CACTGGACCCATCTG	4067
rs116836582	snp	C/T	0.00517822	0.0506191	intron-variant	LYN	GRCh38.p7	8:55925948	ATTTGATTTTAATAT[C/T]GCTTCCAAACATTTT	4067
rs116854174	snp	A/G	0.00953873	0.0683987	intron-variant	LYN	GRCh38.p7	8:55938278	TGCAATGAACAGACT[A/G]GAGTTGTATTTGCAT	4067
rs116865222	snp	C/G	0.00478085	0.0486577	intron-variant	LYN	GRCh38.p7	8:55911528	TGACTCTCCTGGTGA[C/G]CCTGAACTCGTAGGG	4067
rs116868651	snp	C/T	0.00557542	0.0525036	intron-variant	LYN	GRCh38.p7	8:55928437	AGTCATGAGCCACCA[C/T]GCAGGGCCCATTGTT	4067
rs116877072	snp	C/T	0.00676609	0.0577691	intron-variant	LYN	GRCh38.p7	8:55905034	ATTTTTTAGAGTTCC[C/T]CAGGTGATTCTGCTT	4067
rs116946855	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55915347	AAATATATTTTATTA[A/C]ACTCTTTAAAAAAAT	4067
rs116956032	snp	A/G	0.00279162	0.0372561	intron-variant	LYN	GRCh38.p7	8:55939711	TGCTGCTATTAACGT[A/G]TTTGCCCATTTGTAA	4067
rs116965347	snp	C/T	0.0146672	0.084371	intron-variant	LYN	GRCh38.p7	8:55954947	CTAAAGCATAACATT[C/T]TTTTAATGGTTCTAA	4067
rs116977964	snp	C/G	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55993734	GGTGGGGAAATGGTG[C/G]TTATTAATATCCATC	4067
rs117007795	snp	A/G	0.00478085	0.0486577	intron-variant	LYN	GRCh38.p7	8:55892149	CATTAAGGCCAGGGC[A/G]CAGTGGCGCACACCT	4067
rs117025250	snp	A/G	0.00835141	0.0640778	intron-variant	LYN	GRCh38.p7	8:55979533	GTAGCTCTGCAGCTC[A/G]TGGGGCTTTGTGAAA	4067
rs117026752	snp	A/G	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:55882523	TGCCCACAGCAGGGA[A/G]CATTGTTATAAGCTC	4067
rs117035298	snp	A/T	0.0162398	0.0886349	intron-variant	LYN	GRCh38.p7	8:55921099	CATCGTCTAGATACG[A/T]CTGAAACGAAAACAA	4067
rs117055780	snp	A/G	0.0150606	0.0854603	intron-variant	LYN	GRCh38.p7	8:55903947	ATCCGCTTGAGCCTC[A/G]GAGGTTGCAGCTGCA	4067
rs117063411	snp	G/T	0.00716266	0.059414	intron-variant	LYN	GRCh38.p7	8:55924201	GATGTGTGAGAGATG[G/T]CATTGTGTTTCCCTT	4067
rs117076176	snp	C/T	0.0134861	0.0810011	intron-variant	LYN	GRCh38.p7	8:55947916	ATTTTCCTTTTAAGT[C/T]GGTCTGTGAGCACAC	4067
rs117086586	snp	A/G	0.0275645	0.114116	intron-variant	LYN	GRCh38.p7	8:56005454	TGTCCTGCCCTCGGC[A/G]CTGGCCTCCCTCCCT	4067
rs117096036	snp	A/G	0.00358779	0.0422022	intron-variant	LYN	GRCh38.p7	8:56001023	GTGTGGAGCCTGCGT[A/G]GAGTGGCTTAGGGAT	4067
rs117107513	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55918134	GCGCTGATGCTGGCT[C/G]GACTCAGACAGGTCT	4067
rs117132715	snp	A/G	0.0138799	0.0821421	intron-variant	LYN	GRCh38.p7	8:55997662	TTTGGGGTAGGGGGC[A/G]GGGAATGGGACACAA	4067
rs117144143	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55957518	TTGTTCTAGCCTCTC[C/T]TGTTCAGCTGTGAAG	4067
rs117197109	snp	A/G	0.0162398	0.0886349	intron-variant	LYN	GRCh38.p7	8:55905991	GCAGCATAGTTCTAC[A/G]TAACTCACAGCATTC	4067
rs117202649	snp	A/G	0.00597247	0.0543191	intron-variant	LYN	GRCh38.p7	8:55935654	TGGCGGACGCCTGTA[A/G]TCCCCACTACTTGCT	4067
rs117244009	snp	C/G	0.0622301	0.165053	intron-variant	LYN	GRCh38.p7	8:55889303	TGCACCCTTGACCTC[C/G]TGGGCTCAAGCCATC	4067
rs117251957	snp	C/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55928259	CAAGTGATTCTCATG[C/T]TTCACCCTCTGGAGT	4067
rs117267082	snp	A/C	0.00318978	0.0398085	intron-variant	LYN	GRCh38.p7	8:56008242	ATTTGAAAAACACTG[A/C]TTAGAAAATACATTC	4067
rs117286734	snp	A/G	0.0252325	0.109451	intron-variant	LYN	GRCh38.p7	8:55992682	TAGCTTAAGCTTTCA[A/G]GCCTATGATCTAGTG	4067
rs117291131	snp	A/G	0.00318978	0.0398085	intron-variant	LYN	GRCh38.p7	8:55899461	CAGACTTTATACATT[A/G]ACATAAATGTAAACG	4067
rs117396805	snp	A/G	0.0310518	0.120672	intron-variant, downstream-variant-500B	LYN	GRCh38.p7	8:55968113	AGCTCTTGTGGCTTG[A/G]GTTGCCATATATAGC	4067
rs117425257	snp	A/G	0.0130921	0.0798413	intron-variant	LYN	GRCh38.p7	8:55964007	GCTTTTGTTGGTGGA[A/G]TGTACTTTACAATAA	4067
rs117467890	snp	A/G	0.0383715	0.133092	intron-variant	LYN	GRCh38.p7	8:56005526	GAGTTGGGATGGGCC[A/G]CCTTGCCCGTTGTCA	4067
rs117474506	snp	A/T	0.0103295	0.0711199	intron-variant	LYN	GRCh38.p7	8:55970476	GTTTCATTGTGTCCA[A/T]TAGTAATGTTCAGCA	4067
rs117495404	snp	A/G	0.0314385	0.121371	intron-variant	LYN	GRCh38.p7	8:55957342	CCCAATTTTAATCAT[A/G]AAACAGAGCCATAAA	4067
rs117497495	snp	A/C	0.00517822	0.0506191	intron-variant	LYN	GRCh38.p7	8:55894032	AGGCACTGGACCCAT[A/C]TGTGGGTTCATCTTT	4067
rs117560624	snp	C/T	0.0023933	0.0345097	intron-variant	LYN	GRCh38.p7	8:55938649	TTATTTTATTAACTT[C/T]ATTATTGACTCTTTT	4067
rs117591251	snp	C/T	0.0023933	0.0345097	intron-variant	LYN	GRCh38.p7	8:55897242	CTTTGATTCATGTGA[C/T]GCCTATCATGCCATA	4067
rs117593092	snp	C/T	0.0111196	0.0737302	intron-variant	LYN	GRCh38.p7	8:55977437	TCTCCCCCAACACAC[C/T]AGGGTGTTCTTTATA	4067
rs117678169	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55925873	GCAATGAAGAAAAAG[A/G]AAAACCAACTCACCA	4067
rs117695240	snp	C/T	0.00358779	0.0422022	intron-variant	LYN	GRCh38.p7	8:56005295	ATGCATGGTGTGGCC[C/T]ATGTCTTCAGTCTTT	4067
rs117699214	snp	G/T	0.00636936	0.0560724	intron-variant	LYN	GRCh38.p7	8:55963969	ATAATAAAACCTTTT[G/T]GATTTAAATGTAATA	4067
rs117719046	snp	C/T	0.0115144	0.0749975	intron-variant	LYN	GRCh38.p7	8:55920685	TTCAGGAAATTTTTT[C/T]TTTGAGACAGTATCT	4067
rs117784658	snp	A/G	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:55967637	TTAGCGTTATCTAAT[A/G]TTCATTTTCCTTTTC	4067
rs117817671	snp	G/T	0.0178098	0.0926698	intron-variant	LYN	GRCh38.p7	8:55981547	TTAATATAGAGATAG[G/T]GTCTCACTACATTGT	4067
rs117833613	snp	C/T	0.00597247	0.0543191	intron-variant	LYN	GRCh38.p7	8:55906399	TCGCCCAGACTGGAG[C/T]GAAATCACACCCAGC	4067
rs117888545	snp	A/G	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55938718	AGGTAGCCTATAAAA[A/G]TAATCTCTTTGTTTG	4067
rs117894764	snp	A/T	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:55971832	ACCTCGAAGAGTAAT[A/T]TTTCTAACCTAGAAA	4067
rs117977399	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55998195	AGGGCTCAAATGGTG[A/G]TTGCCATTACCCACT	4067
rs118002299	snp	C/T	0.0123036	0.0774623	intron-variant	LYN	GRCh38.p7	8:55954972	TTCTAATGGAATGTG[C/T]GGTTATTTCTGGAAA	4067
rs118017468	snp	A/C	0.00438332	0.0466095	intron-variant	LYN	GRCh38.p7	8:55930134	CCCGCTCTGTGGAAA[A/C]ATTGCCTTCCATGAA	4067
rs118051269	snp	C/T	0.0185938	0.0946107	intron-variant	LYN	GRCh38.p7	8:55987899	ATGGGCTTATTTTAA[C/T]GACTAACATGCCTAG	4067
rs118054509	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:56008186	AAAAGTCAATTTGTT[A/G]ATCCCAAATTGTTGA	4067
rs118093849	snp	A/C	0.00478085	0.0486577	intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55922426	GGTTCTATGTGTGCC[A/C]GTGTATTAATTTATC	4067
rs118106492	snp	C/G	0.0197687	0.0974348	intron-variant	LYN	GRCh38.p7	8:55894640	TGGGTTCAAGCTATT[C/G]TCCTTCTTCAGCCTC	4067
rs118108657	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55939962	TTCAGAAAGAGGTGT[A/G]GCTGCTCTTTAGAGG	4067
rs118113461	snp	A/C	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:55987755	GAGCCAATGTGGATG[A/C]ATGCTTAAGAGCACA	4067
rs118138470	snp	C/T	0.00874735	0.0655527	intron-variant	LYN	GRCh38.p7	8:55885776	AGCAGAACTGTAGCC[C/T]GATGCTGGAGAGAAA	4067
rs118169544	snp	A/T	0.0259391	0.110893	intron-variant	LYN	GRCh38.p7	8:55950647	TTCTTGCCGTGGAAC[A/T]TAATATGCAGGAAAT	4067
rs118170575	snp	C/T	0.00597247	0.0543191	intron-variant	LYN	GRCh38.p7	8:55909639	AGATTGCTGCATCAA[C/T]GGTAGTTCCAGTTTT	4067
rs137924908	snp	G/T	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:55902644	TCCTATGAGATAAGA[G/T]CTGAAAATTCCTTAT	4067
rs137928604	snp	A/T	0.00993419	0.0697739	intron-variant	LYN	GRCh38.p7	8:55978114	CTCAACCAAGTGGCT[A/T]TCCTGGTGCTGTCCC	4067
rs137968857	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55981771	CCTGTACAAAACTTA[C/T]TTCATTGGTTGAAAT	4067
rs138001796	snp	C/G/T	0.0123122	0.0775715	utr-variant-3-prime	LYN	GRCh38.p7	8:56010827	CTCACCCGAAGGCAC[C/G/T]GGGCTCACCTGGACC	4067
rs138049857	snp	C/G	0.00636936	0.0560724	intron-variant	LYN	GRCh38.p7	8:55905800	TGCATCATGTGAGTG[C/G]ATGAAGTCCCTTGCT	4067
rs138058595	snp	C/T	0.00478085	0.0486577	intron-variant	LYN	GRCh38.p7	8:55940078	GCGTGGCAGCGATGC[C/T]GGAGAGGGCCGAGTT	4067
rs138091175	snp	A/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55909696	TTTCCACAGTAGTTG[A/T]ACTAATTTGTATTCC	4067
rs138134532	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55929917	GTACTGGTCTGTGGC[A/C]TGTTAGGAACTGGGC	4067
rs138191921	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55890606	CAAATAACTGAATGT[A/G]GGGTCTCAGAGATGT	4067
rs138207478	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55989640	ATGAGTGCATTCCAC[C/T]CAAATGTTTCTAAAA	4067
rs138240907	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	LYN	GRCh38.p7	8:55876895	ATATTTCATTTTCCC[A/C]CAGTGGATGATGGGA	4067
rs138283635	snp	C/T	0.00676609	0.0577691	intron-variant	LYN	GRCh38.p7	8:55935143	TTAATTGCCCCCAAA[C/T]ACTGTTCCTATTACA	4067
rs138302388	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55920578	AATGAAGTTTAATGA[A/G]GTAACTTGCTTATGT	4067
rs138318076	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55959469	GGTAAGTTCAATTGA[C/T]AGCATTCAAAGCACT	4067
rs138327832	snp	C/T	0.0023933	0.0345097	intron-variant	LYN	GRCh38.p7	8:55994853	GCTATGACCGCTCAA[C/T]TGCTGCTGTCTCATC	4067
rs138348583	snp	A/G/T	0.00478085	0.0486577	intron-variant	LYN	GRCh38.p7	8:55913490	CAACTTGAATAAAAC[A/G/T]ATTAAAGTTGTGCTT	4067
rs138355114	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55963631	GCTCGGCAGTGGTTT[C/T]TCATGACTTTATTTG	4067
rs138430273	snp	C/T	0.00279162	0.0372561	intron-variant	LYN	GRCh38.p7	8:55918068	TGCACTGAGAAGGAA[C/T]CAGGGTGGTCTGGGC	4067
rs138431264	snp	A/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:56005762	CCAAAACTATGATTA[A/T]ATTTCTCTATCAATT	4067
rs138433006	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55965773	GATTATAGCATATAT[A/G]GAGTTTTGTTTTGTT	4067
rs138455996	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55968846	TGACCAAGGCTACCC[A/G]TAAGGCTGGTACTTA	4067
rs138517169	snp	C/T	0.00438332	0.0466095	intron-variant	LYN	GRCh38.p7	8:55908534	CCAGGCCTGAGCCAC[C/T]GTGCCAAGGCTGTTT	4067
rs138539872	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55977418	GTATTCATGTTACCT[C/G]TGTTCTCCCCCAACA	4067
rs138613625	snp	A/G	0.00517822	0.0506191	intron-variant	LYN	GRCh38.p7	8:56002737	ACACCAGAATCCATC[A/G]ACTAGTCTGTTCCCT	4067
rs138623525	snp	C/T	0.00716266	0.059414	intron-variant	LYN	GRCh38.p7	8:56006903	CTTGTCATTTAATAG[C/T]GGATTTTATTTATTG	4067
rs138665381	snp	G/T	0.00517822	0.0506191	utr-variant-3-prime, downstream-variant-500B	LYN	GRCh38.p7	8:56012014	TTTAAAGAAAATTAT[G/T]AAATTTATCTTCGCC	4067
rs138671020	snp	A/G	0.00438332	0.0466095	intron-variant	LYN	GRCh38.p7	8:55905624	TGTCCCAGTTAAGAG[A/G]ATGGATAGTTTCCCA	4067
rs138672337	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55881018	CACTTTTCTGGCTGT[A/G]TATTTAGGGGACCGA	4067
rs138672954	snp	A/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55941356	TCATTTTCTGAAGAG[A/T]TTAGGTTGATCTAGC	4067
rs138694704	snp	A/C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55945232	AAAGCATATTAAAAT[A/C/G]TTTGTAAGTTAAGGG	4067
rs138702253	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55899148	TTACTTTTGTATCAG[G/T]CAATAATTACCTTTC	4067
rs138702341	snp	A/T	0.0524604	0.153226	intron-variant	LYN	GRCh38.p7	8:55944637	AGGCATGCACCACCA[A/T]GCCTGGCTAATTTTT	4067
rs138733978	snp	G/T	0.0283406	0.115616	intron-variant	LYN	GRCh38.p7	8:55949089	CATGCCTGCCTTTCT[G/T]CTGAGGACTCGAGCA	4067
rs138760321	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55953677	CAAAAAAAACCCACA[A/G]ATTTCAAAAGTCACA	4067
rs138763170	snp	A/G	0.0955749	0.196603	intron-variant	LYN	GRCh38.p7	8:55902219	CTACATGTTGGTCAG[A/G]CTGGTCTCGAACTCC	4067
rs138779681	snp	A/T	1.64773e-05	0.00287026	missense	LYN	GRCh38.p7	8:55952014	CTGTGCATGGTGATG[A/T]TATTAAGCACTACAA	4067
rs138795798	in-del	-/TAC	0.0876345	0.190099	intron-variant	LYN	GRCh38.p7	8:56008163	ATAAAATACTGGTAG[-/TAC]TCTAAAAAAGTCAAT	4067
rs138838667	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55910404	TTTATTGAAAAGGGT[A/G]TCCTTTTCCCAGTGT	4067
rs138898294	snp	C/T	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55986061	GTGGTCCCAGTTACT[C/T]AGGAGGCTGAGGTAG	4067
rs138904288	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55973767	TGGAACAATTGTTTG[C/T]GAGTTAAATGTCAGT	4067
rs138939257	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55960462	GACTGAGTTTGCCTG[C/T]CAGTCAGCGAGCTCC	4067
rs138970654	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55925463	CCATATTTCTTTTGC[A/G]TTTAAAATCCTTGGC	4067
rs138989984	snp	C/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55930197	ACTGCTCTAGCTAAC[C/G]TAGACTCCTGATGAT	4067
rs139036235	snp	A/G	0.0150606	0.0854603	intron-variant	LYN	GRCh38.p7	8:55891082	TGCTGGCTGGGTGCG[A/G]TGGCTCATGCCTGTA	4067
rs139038653	snp	G/T	0.0154538	0.0865337	intron-variant	LYN	GRCh38.p7	8:56003339	GTGCTTGGATTACAG[G/T]CACGAGCCACCTCAC	4067
rs139057576	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55994483	AGATTTATGCAAATG[C/T]GGGATGTGGGTAGGT	4067
rs139057994	snp	A/G	0.000115495	0.00759831	synonymous-codon	LYN	GRCh38.p7	8:55953863	GTGCAGAAGATTGGA[A/G]AAGGCTTGTATTAGT	4067
rs139068391	snp	A/G	0.00676609	0.0577691	intron-variant	LYN	GRCh38.p7	8:55891570	TACTGCTTAATGGGT[A/G]CAGAGTTTCAGTTTT	4067
rs139072307	in-del	-/GT			intron-variant	LYN	GRCh38.p7	8:55914100	GGAGGGTTGTTGTTG[-/GT]GTGTGTGTGTGTGTG	4067
rs139081432	snp	C/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55992578	GTTGCATCTGGACTT[C/T]CTCCCCAACCATTAT	4067
rs139088209	in-del	-/A	0.230017	0.2492	intron-variant	LYN	GRCh38.p7	8:55953757	ATAAGGCTAGTGTTC[-/A]AACTTTTCTTTATAG	4067
rs139100202	snp	C/T	0.00398564	0.0444627	intron-variant	LYN	GRCh38.p7	8:55882952	CTGTGTCCCAATAAA[C/T]CCAATCGTAAGTTGA	4067
rs139122364	in-del	-/C			upstream-variant-2KB	LYN	GRCh38.p7	8:55877178	CGGTTCTCCAGTGGG[-/C]CACGCCACAGCCTCT	4067
rs139150526	snp	A/G	0.0185938	0.0946107	intron-variant	LYN	GRCh38.p7	8:55936488	CTACTAAAAACACAA[A/G]AGTTAGCCAGGTGTG	4067
rs139173403	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55958531	GTACAGTTCAGTAGT[A/G]TTAAATGCATCTACA	4067
rs139190135	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55885124	ATGAGCTGACCGTGT[A/G]TGGGAAGAGATTGTC	4067
rs139198891	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55915684	GCACTCCAGCCTGGG[C/T]GAGAAGAGCAAGACT	4067
rs139236226	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55984095	CTCTGACCTTCCTCT[A/G]CCTTCTCTCATAAAG	4067
rs139240757	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55921186	TAATTAAAATATATT[A/C]TATTACGGAATTGCT	4067
rs139383168	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55991362	TGCCTCAAAGCCCTG[A/G]CTTATGGAAGGCATC	4067
rs139433081	snp	A/G	0.00279162	0.0372561	intron-variant	LYN	GRCh38.p7	8:55883222	GCCTAATGCTTTTGC[A/G]CCATCGTAAAGTTGA	4067
rs139465770	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55970007	AGTTTTGACCTGGAT[A/T]TCATCTTCTATAAAC	4067
rs139473254	snp	A/T	0.00597247	0.0543191	intron-variant	LYN	GRCh38.p7	8:55932919	CTAGGCATTGAATAC[A/T]TATGGATGTAAAGAT	4067
rs139513631	snp	C/G	0.00438332	0.0466095	intron-variant	LYN	GRCh38.p7	8:55927547	TCAATTAGGAATAAA[C/G]CTGCTGGCCAGGTGC	4067
rs139531443	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55911872	ATGGAGAAGATGGGA[A/G]GGGAGTGGGTTTCAA	4067
rs139570859	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55975999	TCTTATCTTAATGTT[A/C]TTTTGACCAGGGGTG	4067
rs139577116	snp	A/C	0.00478085	0.0486577	intron-variant	LYN	GRCh38.p7	8:55900175	CTTGGTGCAATTTTT[A/C]CTATAACCATAGCTG	4067
rs139614979	snp	C/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55976516	TATCCTGAGCACAGC[C/G]AGGCACTGTGTCAGG	4067
rs139618977	snp	C/T	0.00478085	0.0486577	intron-variant	LYN	GRCh38.p7	8:55901095	CCATACTGCCAGTGC[C/T]TTTGCTCAGCACTTG	4067
rs139643129	snp	C/G	0.00517822	0.0506191	intron-variant	LYN	GRCh38.p7	8:55903325	GGAAGTTGTCTTCAT[C/G]GTGAGCAGCTCTTCT	4067
rs139701376	snp	A/G	0.00398564	0.0444627	intron-variant	LYN	GRCh38.p7	8:55903731	TGTAGAATTTAAAGT[A/G]TTTTATCCATGGTAG	4067
rs139765598	snp	A/G	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55970521	TTCTCAGTATTGGCA[A/G]TCGGTGGTTTCATGA	4067
rs139801782	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55975471	CTTTTATTTAGACTA[C/T]CTATGTGAATCGTCA	4067
rs139817386	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55995775	GAGGTGGAGGGCTGA[A/G]CCGGGGCCGGGTCAT	4067
rs139862376	snp	C/G	0.0441095	0.141807	intron-variant	LYN	GRCh38.p7	8:55884171	GTGGTGCAATCTCAG[C/G]TCACGGCAATCTCCG	4067
rs139863523	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55957422	TGTCTGTCATGAAAA[A/G]AAATGTAGAGGGAGG	4067
rs139882963	snp	C/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55961159	TGCATTTTTTAAAAA[C/T]CACTCTCCCTTTTGT	4067
rs139883711	snp	C/G	0.00716266	0.059414	intron-variant	LYN	GRCh38.p7	8:55888644	CAGCAATAGGCTTCA[C/G]CTTGTAATCGTCATC	4067
rs140021610	snp	A/G	0.00398564	0.0444627	intron-variant	LYN	GRCh38.p7	8:55946614	ATAACATAAAAATTT[A/G]CCCTCTTAACTATTT	4067
rs140030453	snp	A/G	0.00438332	0.0466095	intron-variant	LYN	GRCh38.p7	8:55979732	TCTCACCCTGATTCA[A/G]CGTCACCCCAGGAAA	4067
rs140071517	snp	A/C/G	0.00676609	0.0577691	intron-variant	LYN	GRCh38.p7	8:55937237	GGTGGTGGATGTCCT[A/C/G]TTAGATTTTTTTCCT	4067
rs140096312	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55943617	TTATAGTTTCTCTAG[C/T]CTGACATGTTTTTAA	4067
rs140137648	snp	A/G	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:55944761	GTTGGGAATACAGGC[A/G]TGAGCCACCACACCC	4067
rs140156584	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55887436	ATTTCTGGGTGACAG[C/T]TGAGTGCTGTTTTTA	4067
rs140189894	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55950879	GAAAAAAGGGCATAT[A/G]GTATGCTCTGGTAGT	4067
rs140215306	snp	C/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55957859	AGGTTGAGGTGGGAG[C/G]ATCGCTTGAGCCTAG	4067
rs140218412	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55907079	AAGGAATTCCACTTC[C/T]AGATATTAATCCAAG	4067
rs140220848	snp	G/T	0.0023933	0.0345097	intron-variant	LYN	GRCh38.p7	8:55909154	CTTCTCTGCTAAGTA[G/T]GAAACCCTGACCCAG	4067
rs140232830	snp	A/G	0.00478085	0.0486577	upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55879141	CCAGCTGCTACGTGC[A/G]AGCACTGCCCTACAT	4067
rs140240599	snp	C/G	0.00517822	0.0506191	intron-variant	LYN	GRCh38.p7	8:55912060	GCTCAAATGGAAGGA[C/G]AGAGGAACAACTTAG	4067
rs140249274	snp	A/G	0.00557542	0.0525036	intron-variant	LYN	GRCh38.p7	8:55989464	TGATGACACAAAACC[A/G]CAGTGCCTCATGAGG	4067
rs140376090	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55996739	TGACTTTGGAACGAT[A/G]CTACACTTTCTATTC	4067
rs140382586	snp	A/G	0.00517822	0.0506191	intron-variant	LYN	GRCh38.p7	8:55953061	GAGCAACGTGCTTCC[A/G]ATTTTGTAGATTCTT	4067
rs140384657	in-del	-/T			intron-variant	LYN	GRCh38.p7	8:55883862	GAGGAAGTTGTTGGG[-/T]TTTTTTTTTCCAGTC	4067
rs140407767	snp	A/G	0.00318978	0.0398085	intron-variant	LYN	GRCh38.p7	8:55884401	TGAGCCACTGCGCCT[A/G]GCCTTTCTGGGGTAT	4067
rs140479145	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime	LYN	GRCh38.p7	8:56010238	GGATCCTGAAATAGA[A/G]GCTAAATTACTCAGG	4067
rs140481302	snp	C/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55893725	AAACTGTTCCAGATA[C/T]ACTCAGAGAGTTAAA	4067
rs140494188	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55929650	GACATTTTTGGTTGT[C/G]ACAACTGGTAGCTGG	4067
rs140518667	snp	A/G	0.00597247	0.0543191	intron-variant	LYN	GRCh38.p7	8:55897678	GCACTTTGGGAGGCC[A/G]AGGCAGGAAGATCAC	4067
rs140550331	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56001210	AGGAGGCCAGCGTGG[A/T]TTGGGCCTCTGTGAG	4067
rs140557050	snp	A/G	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:55901752	TCAGATATTTCCAAC[A/G]CGGAGCTGGATGTGG	4067
rs140572905	snp	A/T	0.0475351	0.146656	intron-variant	LYN	GRCh38.p7	8:55977190	GACTCTGTCTCAAAA[A/T]AAAAATAAAAATAAA	4067
rs140609013	snp	C/T	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55933399	TTTCTATATGGTATT[C/T]CAAACAGTCCCACAA	4067
rs140614548	snp	A/G	1.65466e-05	0.00287628	missense, intron-variant	LYN	GRCh38.p7	8:55941902	GACAGCTTGAGTGAC[A/G]ATGGAGTAGATTTGA	4067
rs140648136	snp	A/T	0.00438332	0.0466095	intron-variant	LYN	GRCh38.p7	8:55936034	AGTAAAGTAAGAAGG[A/T]CAATTAAAGGGTATC	4067
rs140648228	snp	C/G	0.00835141	0.0640778	intron-variant	LYN	GRCh38.p7	8:55891840	TGGGTATTTACCTAC[C/G]AAGCAGACGGGTGTT	4067
rs140673970	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55917264	GATTGTAGGTCACTG[A/C]AGCCTTGAACTCCTA	4067
rs140708577	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56005448	AGGTACTGTCCTGCC[C/T]TCGGCGCTGGCCTCC	4067
rs140711956	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55905306	GATTCCAGCTACTCC[A/G]GAGGCTGAGCAGGAG	4067
rs140734985	snp	G/T	0.00358779	0.0422022	upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55877838	AGAGAAAACTGGTGA[G/T]ATAAATCAGTCATCA	4067
rs140771921	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55948558	CAGACCATAGGCATG[C/T]AGGACAGTGCTCAGA	4067
rs140771981	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55993273	TTTGCATGTACTTCC[C/T]GAAATGGGAACCAGA	4067
rs140808795	snp	A/G	0.0115144	0.0749975	intron-variant	LYN	GRCh38.p7	8:55880186	GTGCCACCAGCCGGA[A/G]TCCCGGGCGCAGGGT	4067
rs140810862	snp	C/T	0.134119	0.221521	intron-variant	LYN	GRCh38.p7	8:55952452	GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG	4067
rs140872933	snp	A/G	0.00438332	0.0466095	intron-variant	LYN	GRCh38.p7	8:55962662	TGCTGTGCTGCATGT[A/G]TTTTCAAGATATACG	4067
rs140930690	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55984508	AAAGTCATTCTTGAC[C/T]CTCTTCCTTTTACAT	4067
rs140957934	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56004971	TAAATTTTTTGTAGA[G/T]ACAGGGTCTCACTAT	4067
rs140976457	snp	A/C	3.29527e-05	0.00405898	synonymous-codon	LYN	GRCh38.p7	8:55999509	GTCCTTTGGAATCCT[A/C]CTATACGAAATTGTC	4067
rs141018197	snp	A/G/T	0.00716266	0.059414	intron-variant	LYN	GRCh38.p7	8:55911412	CGGGCGTGAGCCACC[A/G/T]CACCCAACCGGTTTT	4067
rs141041134	in-del	-/AGAGA			utr-variant-5-prime, frameshift-variant	LYN	GRCh38.p7	8:55879825	CTCTCGGCCGAGCCC[-/AGAGA]CAGCCAGTTCCTCTC	4067
rs141055956	snp	A/G	0.00358779	0.0422022	intron-variant	LYN	GRCh38.p7	8:55914089	AATGGAGAGGTGGAG[A/G]GTTGTTGTTGGTGTG	4067
rs141070411	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	LYN	GRCh38.p7	8:56010468	AAGTTTCAGAGACCA[C/T]TGCAATGAATCCCCA	4067
rs141179582	snp	C/G	0.00398564	0.0444627	intron-variant	LYN	GRCh38.p7	8:55929977	CAAGCATTACTGCCT[C/G]AACTCTGTCTCCTGT	4067
rs141191081	snp	A/G	0.021333	0.101051	intron-variant	LYN	GRCh38.p7	8:55932118	CCTGAAATAAGGAAA[A/G]GAAGTGTTCCTGTGC	4067
rs141193094	snp	A/G	0.0345262	0.126772	intron-variant	LYN	GRCh38.p7	8:55976977	ATCACCTGAGGTCAG[A/G]AGTTTGAGACCAGCC	4067
rs141207667	in-del	-/T	0.00398564	0.0444627	intron-variant	LYN	GRCh38.p7	8:55897793	TGGCATGGGCCTGTA[-/T]TCCCAGCTACTCAGG	4067
rs141211094	snp	C/T	0.0023933	0.0345097	intron-variant	LYN	GRCh38.p7	8:56002803	ATATCTTCAGGAGAT[C/T]GGGATCAGTAAATTT	4067
rs141211670	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55977528	CATTTTGTTTTATTA[C/T]TGTTTTTGTTGCTGT	4067
rs141238789	snp	A/G	0.0023933	0.0345097	intron-variant	LYN	GRCh38.p7	8:55912591	AATTAACTGGGCATC[A/G]TGGCACATGCCTGTA	4067
rs141259265	snp	A/G	0.00874735	0.0655527	upstream-variant-2KB	LYN	GRCh38.p7	8:55876684	GTCTGTGGCCAAGTT[A/G]GCAAGAGTTAGGTGG	4067
rs141288592	snp	A/G	0.0189856	0.0955633	intron-variant	LYN	GRCh38.p7	8:55979169	TGCCTCAGCCTCCCG[A/G]GTAGCTGGGATTACA	4067
rs141306138	snp	A/G	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55963105	CAACATGAGATTTGG[A/G]GAGGACAAACATCCA	4067
rs141328910	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55936085	GGCAAAGTAAATCTC[C/T]TGAGTTATAGAACTG	4067
rs141351914	snp	A/G	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:55892318	CCAGCTACTTGGGAG[A/G]CTGAGGCAGGAGAAT	4067
rs141389031	in-del	-/TC			intron-variant	LYN	GRCh38.p7	8:55949738	GGCTTCTTTTCTTTG[-/TC]TCTCTCTCTCTCTTT	4067
rs141412991	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55973200	TGTCACCCATTGAGA[C/T]AGAAAGTGGCTAAGT	4067
rs141429700	snp	C/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55983720	GGCTTCTGGGACACT[C/G]TTCTCTGCTTTTCCT	4067
rs141560809	snp	A/G	0.0383715	0.133092	intron-variant	LYN	GRCh38.p7	8:56000479	TACACCTGTAATCCC[A/G]GCACTTTGGGAGGCT	4067
rs141566724	snp	C/T	0.00517822	0.0506191	intron-variant	LYN	GRCh38.p7	8:55964607	CACAGTGGCTCATGC[C/T]TACAATCCCAGCACT	4067
rs141596743	snp	C/T	0.00279162	0.0372561	intron-variant	LYN	GRCh38.p7	8:55998830	AATGAATATAATATA[C/T]GGGGCTGTGGAGAAA	4067
rs141635595	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55958933	TGGGTGCACAGATAC[C/T]TCTCTGAGACCTTAT	4067
rs141635759	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56001736	TCTGTAGAGAAAGAT[G/T]ATATAGTCAGATTAT	4067
rs141645695	snp	A/T	0.00716266	0.059414	intron-variant	LYN	GRCh38.p7	8:56006174	TTGAAAGTGAAAAAA[A/T]TTTCTGAAGCATCAT	4067
rs141674473	snp	C/T	0.00478085	0.0486577	intron-variant	LYN	GRCh38.p7	8:55895351	GAGATGGGGAAATAA[C/T]TTGGCTGGATTCCTT	4067
rs141678193	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55890339	AACAATAATAAAAAG[A/C]AAGTTGCTTAGGATG	4067
rs141691984	snp	A/G	0.00343774	0.0413165	intron-variant	LYN	GRCh38.p7	8:55969823	AAGCCCCGTGTGCAC[A/G]TGCATTTGCAAAGAC	4067
rs141712280	snp	C/G	0.134119	0.221521	intron-variant	LYN	GRCh38.p7	8:55944574	CAACCTCCTCCTCCT[C/G]AGTTCAAGCGATTCT	4067
rs141719744	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55953391	GGTGGCTCACACCTG[C/T]AATCCAGCATTTTGG	4067
rs141748617	snp	A/G	0.00795532	0.062565	downstream-variant-500B	LYN	GRCh38.p7	8:56012784	TGCTCAGTCTTGAGA[A/G]TCACCATTTGGTTTG	4067
rs141750227	snp	A/G	0.00517822	0.0506191	intron-variant	LYN	GRCh38.p7	8:55946686	TGTACAACCAATACC[A/G]CCCTCCATCTCCAGA	4067
rs141769918	snp	A/G/T	0.000148772	0.00862356	missense	LYN	GRCh38.p7	8:55950745	GCACCAGGAAATAGC[A/G/T]CTGGAGCTTTCCTTA	4067
rs141774283	snp	C/T	0.00557542	0.0525036	intron-variant	LYN	GRCh38.p7	8:55899556	ACACGGTATGTCATT[C/T]GTTCTTCTAAACACT	4067
rs141789686	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55949104	GCTGAGGACTCGAGC[A/G]TGGTGCTGAAGCTCA	4067
rs141795927	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55903139	TGCGTGAGCCACTGC[A/G]CCCGGCCTACGCCCA	4067
rs141816369	snp	C/T	0.0023933	0.0345097	intron-variant	LYN	GRCh38.p7	8:55960139	AACTGATGAACTATA[C/T]ACTTTAAATGGGTAA	4067
rs141818686	snp	A/C	0.00676609	0.0577691	intron-variant	LYN	GRCh38.p7	8:55987564	TGGGATTATGGGTGC[A/C]CGCCACCACACCTAG	4067
rs141835189	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55905665	CCTTTCTTTTCCTAG[C/T]CACCCCCAAACACTT	4067
rs141926209	snp	A/G	0.00795532	0.062565	intron-variant	LYN	GRCh38.p7	8:55891485	TGAGGTTCCTCAAAT[A/G]GTCAAATTCATAGAG	4067
rs141941484	in-del	-/TT			intron-variant	LYN	GRCh38.p7	8:56008741	TAATGAGCACCTTAC[-/TT]TTCTCTCCTGGAGGT	4067
rs141999680	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55982107	AGGGTGATGGGCTGG[C/T]GGATTCTTAACAAAG	4067
rs142017308	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55999349	AAAAGAAAGTATGGG[A/G]TCACATGTTCATGAC	4067
rs142035525	snp	A/G	0.00597247	0.0543191	intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55922999	CTTTCCGAGCCTAGA[A/G]TCCAAGTGCAATTAT	4067
rs142038418	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55940761	TCACCTTTGCAGTCC[C/T]CAGAGTGCGTGTGTA	4067
rs142087237	in-del	-/TA	0.418491	0.184691	intron-variant	LYN	GRCh38.p7	8:55957190	GACAAACTCCAATCT[-/TA]TCAGTTGTTCAAAGG	4067
rs142099650	snp	C/T	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55927098	GCCAATGTTGATACA[C/T]TAATTAAAATCTACA	4067
rs142102649	in-del	-/G	0.285592	0.254789	upstream-variant-2KB	LYN	GRCh38.p7	8:55877282	TAATTTTTTTATTGT[-/G]GGGGGGGGTCTCACG	4067
rs142137571	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55997618	TCCTAATACTATTGC[C/T]TCGGGGTTCAGGATT	4067
rs142141277	snp	C/T	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55923869	AATAAATGTTTGTTA[C/T]AATGACTTAGTGCCA	4067
rs142191333	snp	C/T	0.00993419	0.0697739	intron-variant	LYN	GRCh38.p7	8:55887741	CAGCCTCCTGAGTAG[C/T]TGGAATTACAGGCAC	4067
rs142191673	snp	C/T	0.00438332	0.0466095	intron-variant	LYN	GRCh38.p7	8:55930742	ATGTTGATGGGGGAC[C/T]AAGACCTGGTCTTGC	4067
rs142228114	snp	G/T	0.0603597	0.1629	intron-variant	LYN	GRCh38.p7	8:55891143	GGATCACCTGAGGTC[G/T]GCAGTTTGACACCAG	4067
rs142233085	snp	A/G	0.0107246	0.0724382	intron-variant	LYN	GRCh38.p7	8:55967290	TACGGATTGTTCAGT[A/G]CCAAATTCCTCTTTC	4067
rs142271340	snp	C/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55889775	TAGAGCACAGGGTGT[C/T]GAATTAATTTCATGT	4067
rs142291090	snp	C/T	0.000992424	0.0222537	synonymous-codon	LYN	GRCh38.p7	8:56009921	AGGGAGAACTAATGC[C/T]GACGTGATGACCGCC	4067
rs142299350	snp	C/T	0.0103295	0.0711199	intron-variant	LYN	GRCh38.p7	8:55906488	CAGCCTCCCAAGTAG[C/T]TGGGATTACATGTGC	4067
rs142361740	snp	C/G	0.00636936	0.0560724	intron-variant	LYN	GRCh38.p7	8:55971462	GGTGATTTGGGTGTC[C/G]CCATGGGTCAAGAGA	4067
rs142413131	snp	A/C	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55993989	AGTGCTGAACGCTAC[A/C]TGGCCCTGGAAGAGG	4067
rs142425171	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55911503	ACCATCTCTTTTGTA[C/T]AGACTGAGATGACTC	4067
rs142487297	snp	A/G	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55962466	TCTTCATCTCATGTC[A/G]TGTTTGTGAGATGCA	4067
rs142489448	snp	C/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55889332	TCTTCCCACTTCAGC[C/T]TCCAAGTAGCTGGGA	4067
rs142506908	snp	A/G	0.0142736	0.0832652	intron-variant	LYN	GRCh38.p7	8:55981498	AATGAGTAACTAGAA[A/G]AACATATTTTTTGTG	4067
rs142526837	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55905926	TTCATCTTGACTTCT[A/G]GAAAGAAGCCTATAG	4067
rs142567297	snp	C/T	0.00755907	0.0610114	intron-variant	LYN	GRCh38.p7	8:55910055	ATATTAGTCCTCTGT[C/T]GAAGGCATAGTTTGC	4067
rs142611226	snp	C/T	0.00279162	0.0372561	intron-variant	LYN	GRCh38.p7	8:55985974	GAGTTCGAGACCCGC[C/T]TGGGCAATATAGTGA	4067
rs142675751	snp	C/G	0.00914312	0.0669923	utr-variant-3-prime	LYN	GRCh38.p7	8:56012383	TACCGCCAAGATTCT[C/G]ACTTAGCTGTTGTGC	4067
rs142675796	snp	G/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55970246	CCTGCTCCTCTTCTC[G/T]CTCCTTCTTGTTGGA	4067
rs142711988	snp	C/T	0.0298908	0.118541	intron-variant	LYN	GRCh38.p7	8:56000676	CAGGTTGCAGTGAGC[C/T]GAGACTGCACCCCTG	4067
rs142722056	snp	C/T	0.00914312	0.0669923	intron-variant	LYN	GRCh38.p7	8:55899337	GGAACCCAAGTCAGC[C/T]GGACCCCTAAACTGA	4067
rs142723210	snp	A/G	0.00279162	0.0372561	intron-variant	LYN	GRCh38.p7	8:55975117	TCTGAGCCGGGTGCC[A/G]CTGTGGATTCAGGGG	4067
rs142777324	snp	C/T	1.648e-05	0.0028705	synonymous-codon	LYN	GRCh38.p7	8:55952048	TAGAAGTCTGGATAA[C/T]GGGGGCTATTACATC	4067
rs142840592	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55946390	TCATATATACAACAC[A/G]AATGTGAGTAAGAAA	4067
rs142873245	snp	A/G	0.0142736	0.0832652	intron-variant	LYN	GRCh38.p7	8:56004578	GGATTACAGGCATGA[A/G]CCACCGTGTGCAGCC	4067
rs142915348	snp	G/T	0.0228947	0.104514	intron-variant	LYN	GRCh38.p7	8:56006965	ATTCCCTTCTTCCAA[G/T]TCTTCTTATCAAGTC	4067
rs142919847	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55992548	CACATCTTACTCCTT[C/T]TTTTGTTAAGCTGAG	4067
rs142941974	snp	A/G	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55981268	ATTCTCCTCAGTCTC[A/G]GTCCCCGCCCATTTC	4067
rs142946786	snp	A/G	0.000445467	0.0149176	intron-variant	LYN	GRCh38.p7	8:55950640	CACCTTTTTCTTGCC[A/G]TGGAACATAATATGC	4067
rs142949268	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55878823	AAATAACTGCTGTAT[C/T]AGATTGTGTCACAAG	4067
rs142958976	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55994674	GCTATTGTCAACTGT[A/G]GTTTCAGGCCCAATT	4067
rs143002509	snp	C/T	0.00478085	0.0486577	intron-variant	LYN	GRCh38.p7	8:55883000	GATGCATTTAATACA[C/T]TTAACCTACTAAACA	4067
rs143053736	in-del	-/TG			intron-variant	LYN	GRCh38.p7	8:55967331	TTTTTTTTTTTTTTT[-/TG]GAAACAGAGTCTCAC	4067
rs143057145	snp	A/G	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55953733	CACAGACTGCGGCAG[A/G]TTGGACACTATAAGG	4067
rs143083385	in-del	-/C	0.0252325	0.109451	intron-variant	LYN	GRCh38.p7	8:55886074	GTACATTTTGAAATT[-/C]CCCGTCATGGAAAGT	4067
rs143085062	snp	A/G	0.00279162	0.0372561	intron-variant	LYN	GRCh38.p7	8:55974818	CCTTTGATTGATAGC[A/G]TCCTCATGTTTAGTT	4067
rs143103162	snp	A/G	0.00478085	0.0486577	intron-variant	LYN	GRCh38.p7	8:55886081	TTGAAATTCCCCGTC[A/G]TGGAAAGTGTTATGA	4067
rs143154559	snp	C/T	0.00716266	0.059414	intron-variant	LYN	GRCh38.p7	8:55995792	CGGGGCCGGGTCATA[C/T]GGGGCCTTGGCAGCA	4067
rs143195112	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55957428	TCATGAAAAGAAATG[C/T]AGAGGGAGGTTAATC	4067
rs143235719	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55963699	CGTGTTTATTACTCA[C/T]ATGAATTTCTTCTTT	4067
rs143246295	snp	A/G	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55888815	GATCTCACTCACCAG[A/G]GATTTGGCCACCACG	4067
rs143285028	snp	C/T	0.00517822	0.0506191	intron-variant	LYN	GRCh38.p7	8:55961937	GACCTTCCTGATGGT[C/T]TTCTGACTTCTTCTT	4067
rs143329919	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55991476	TCTAGATGACTGGAA[A/G]TCTATCTATCCAGCC	4067
rs143333130	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55900634	GGTCCTCCAGTCTTG[A/G]CCTCCCAAAGTATTG	4067
rs143368606	snp	A/G	0.00398564	0.0444627	intron-variant	LYN	GRCh38.p7	8:55978187	GCCTGGGGATAATGG[A/G]GATCGACTGAGCATT	4067
rs143378787	in-del	-/A	0.100231	0.200173	intron-variant	LYN	GRCh38.p7	8:55898133	TGACACCCTCCCCCC[-/A]AAAAAAAAACTTTCT	4067
rs143405646	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55901651	TGAATATTTTCAGTG[C/T]TGATTCAGAAAGAGC	4067
rs143464500	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55948398	CTGGGTTCATGGGCC[C/T]AGCCTAGCTTGAGTT	4067
rs143487683	snp	A/G	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55993407	AGAAGTACTCTCTCA[A/G]TGAAATCTTTGGGTT	4067
rs143501793	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56006104	AAAGGTGGGGGTGTC[A/T]TGTTGGGGTCCTGGT	4067
rs143502905	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55935160	CTGTTCCTATTACAC[A/G]TGACATTTAAACCTT	4067
rs143505781	snp	A/G	0.00755907	0.0610114	intron-variant	LYN	GRCh38.p7	8:55905271	CAAAAAATTAGCCAG[A/G]CGTGGTGGCAGGCAC	4067
rs143568644	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55953266	ACAATCTGGCAGCCT[C/G]TGGTTGTCTGTTGGC	4067
rs143569432	snp	A/G	0.00597247	0.0543191	intron-variant	LYN	GRCh38.p7	8:55881870	AATGATAGCCCCAGT[A/G]CCTGGTACATAGTAG	4067
rs143597909	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55882668	CTTTACTGGCTCTTC[C/G]TAGTGATGATGGTGA	4067
rs143618927	snp	A/C	0.000214736	0.0103596	synonymous-codon	LYN	GRCh38.p7	8:55950735	GCAGCTTTTGGCACC[A/C]GGAAATAGCGCTGGA	4067
rs143623026	in-del	-/ATTTATTT			intron-variant	LYN	GRCh38.p7	8:55908223	TAAGCTGTTTAAACC[-/ATTTATTT]ATTTATTTATTTATT	4067
rs143625316	snp	C/T	0.00676609	0.0577691	intron-variant	LYN	GRCh38.p7	8:55937840	AGCTGGGACTACAGA[C/T]GGGTGCCACCACACC	4067
rs143645403	snp	A/G	0.00438332	0.0466095	intron-variant	LYN	GRCh38.p7	8:55999269	AGGTTGCAGTGAGCC[A/G]AGATCGCATCATTAC	4067
rs143655358	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55924705	GGATCCAGCCATGAC[C/T]TTCCATTTCCTCTTT	4067
rs143676517	snp	C/T	0.00953873	0.0683987	intron-variant	LYN	GRCh38.p7	8:55886082	TGAAATTCCCCGTCA[C/T]GGAAAGTGTTATGAA	4067
rs143745950	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55975482	ACTATCTATGTGAAT[C/T]GTCACCAAAAGTTGC	4067
rs143749858	in-del	-/C	0.0337553	0.125452	intron-variant	LYN	GRCh38.p7	8:55945730	CTTCCCAATAACTCA[-/C]CCCCCCCACTGAAAT	4067
rs143756160	snp	C/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55883738	CGCACATTAAAACAC[C/T]TGATCATTTTGAGCA	4067
rs143826940	snp	C/T	0.0123036	0.0774623	intron-variant	LYN	GRCh38.p7	8:55938222	GTAATCAAAAGGCTG[C/T]CTGGCCGTTTGTGTC	4067
rs143856948	snp	A/C	8.23703e-05	0.00641704	missense	LYN	GRCh38.p7	8:55953945	TCCATCAAGTTGGTG[A/C]AAAGGCTTGGCGCTG	4067
rs143866436	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55967099	TTGAAATCTAATCCT[C/T]CTGTTTTCTCTGCAT	4067
rs143882129	snp	A/C	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55913522	CTGAATTTCAACTAC[A/C]TTAAAGGTACCAGTG	4067
rs143905761	snp	A/G/T	0.00915364	0.0671472	intron-variant	LYN	GRCh38.p7	8:55918093	CTGGGCTGTGGTAGC[A/G/T]GCAGCAGCAGCTTGC	4067
rs144007179	snp	C/T	0.00676609	0.0577691	intron-variant	LYN	GRCh38.p7	8:55993049	TTGATCCCTTAGGGG[C/T]GATAAAAATCTTAGA	4067
rs144012041	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55915838	AGAGAGCGAGCGAGC[A/G]AGAGACATCGAGGAT	4067
rs144031694	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55879209	GCATTCCTGCATGCG[A/G]GCAGTGCGGGCCCTG	4067
rs144054343	snp	G/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55995311	TTGAATCTTTTCCAG[G/T]GTCAGGTAAAAGCTG	4067
rs144115759	snp	A/G	0.00795532	0.062565	intron-variant	LYN	GRCh38.p7	8:55955600	TACATTCACAATATT[A/G]TGTAGCCACCACCTC	4067
rs144150282	snp	A/G	0.00438332	0.0466095	intron-variant	LYN	GRCh38.p7	8:55978408	CGCCATTGCGGGCAC[A/G]GGGTTGAGGTGGCTG	4067
rs144157801	in-del	-/T	0.021333	0.101051	intron-variant	LYN	GRCh38.p7	8:55894072	CCACTAAGGGACCCA[-/T]CTTTCTGTGAAAAAG	4067
rs144216436	snp	C/T	0.00318978	0.0398085	intron-variant	LYN	GRCh38.p7	8:55976828	CAGAAAAGGAGTACA[C/T]GGGGATGCAAGTGGG	4067
rs144229629	snp	A/G	0.00676609	0.0577691	intron-variant	LYN	GRCh38.p7	8:55901369	TGTCTGATGAAGTCA[A/G]TGTAAGTGATGGTAT	4067
rs144266900	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55950106	ATCTCTCAGCACTCC[A/T]TTCCTTTCACTGCTG	4067
rs144272098	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55903409	AATGAAAATATTAAG[C/G]CTTCTATATCATGCC	4067
rs144292199	snp	A/G	0.00438332	0.0466095	intron-variant	LYN	GRCh38.p7	8:55906290	TACCAGTACTTTGGG[A/G]GGCTGAGGTGGGAGG	4067
rs144309875	snp	C/T	0.0023933	0.0345097	intron-variant	LYN	GRCh38.p7	8:56009645	GGATTAAGACCTACC[C/T]AAATGGCCTCATTTT	4067
rs144320911	snp	G/T	0.00358779	0.0422022	intron-variant	LYN	GRCh38.p7	8:55979647	TGAGGTCAGTTTGGT[G/T]CCTGGAATGCATTCC	4067
rs144330348	snp	A/G	0.0023933	0.0345097	intron-variant	LYN	GRCh38.p7	8:55994980	CACATGCTCAGCCTG[A/G]TCTTCGCTCTCCACT	4067
rs144335088	snp	C/T	3.29924e-05	0.00406142	missense	LYN	GRCh38.p7	8:55998373	ATGGCATACATCGAG[C/T]GGAAGAACTACATTC	4067
rs144353246	snp	A/G	0.00358779	0.0422022	intron-variant	LYN	GRCh38.p7	8:55883627	CGACCTGTGCTGGGA[A/G]TGTCTCCCTGTAAAC	4067
rs144362861	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55929116	TATTTGTGTGGTTCT[A/G]TTTCTGGGCTGTTTA	4067
rs144375678	snp	C/T	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55956302	ACATGTTATTATTGC[C/T]GTTGACCACCTGAGA	4067
rs144381182	in-del	-/T	0.26326	0.249648	utr-variant-3-prime	LYN	GRCh38.p7	8:56010729	ACTGCTCAGACCTGC[-/T]TAGACATGCCATAGG	4067
rs144408332	snp	C/T	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:56001268	TGAATGAATGAATGA[C/T]GCACCTAGGCCATTT	4067
rs144428385	snp	A/C			missense	LYN	GRCh38.p7	8:55947672	CCTATGATGGCATCC[A/C]CCCGGACGACTTGTC	4067
rs144431778	in-del	-/TGA	0.0501905	0.150254	utr-variant-3-prime, downstream-variant-500B	LYN	GRCh38.p7	8:56012185	CACACGTTCCCTTGA[-/TGA]ACAGCACACACAGTC	4067
rs144431963	snp	C/T	0.0142736	0.0832652	intron-variant	LYN	GRCh38.p7	8:56000544	CCAGCCTGGCCAACA[C/T]GGTGAAACCCCGTCA	4067
rs144433635	snp	A/C	0.0142736	0.0832652	intron-variant	LYN	GRCh38.p7	8:55927642	GAGTTCGAGACCAGC[A/C]TGGCCAACATGGTGA	4067
rs144496336	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55892026	GTAAGGAGAAACTTC[G/T]AACCATCAAAGCTGC	4067
rs144507495	snp	A/G	0.00199481	0.0315187	utr-variant-3-prime	LYN	GRCh38.p7	8:56010413	TCTCTCCAAAAATGC[A/G]CCCAACTAGCTCTAT	4067
rs144561586	snp	C/T	0.00914312	0.0669923	intron-variant	LYN	GRCh38.p7	8:55880751	GTCCGGTGCTTTTGC[C/T]GGCTGAGAGGAAGCG	4067
rs144579824	in-del	-/ATATATATATATACACACACACACACACACAC			intron-variant	LYN	GRCh38.p7	8:55908999	TGTATGTATATATAT[lengthTooLong]ACACACACACACACA	4067
rs144586058	snp	A/G	0.00953873	0.0683987	upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55878298	GGAGTTAGGGAGTTG[A/G]GGATCTGGTTGCAAG	4067
rs144587505	snp	C/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55982528	TTTCCAGACCTTCTA[C/T]CTCCCCCACCCAGGA	4067
rs144599823	snp	A/G	0.0494327	0.149241	intron-variant	LYN	GRCh38.p7	8:55952453	TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG	4067
rs144623169	snp	C/T	0.00318978	0.0398085	intron-variant	LYN	GRCh38.p7	8:55942953	AAATAGTACAGATCC[C/T]GAAGTTGTCATCTGT	4067
rs144717159	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55987155	CTGTGGCTCATGCGT[A/G]TAATTTCAGCACTTT	4067
rs144753711	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55976161	AGTTGAAAAGTGGAG[A/T]TGAAAGCAGTTTGAA	4067
rs144755094	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55985989	CTGGGCAATATAGTG[A/G]GACCTCATCTCTACA	4067
rs144759031	in-del	-/T	0.0737376	0.17729	intron-variant	LYN	GRCh38.p7	8:55889147	TCAGTACTGGGTAGC[-/T]TAGGATTACAGGCCC	4067
rs144811196	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55984575	CCTCAAAGTAGATTC[A/G]CCTTCCTAAGTCCTG	4067
rs144825104	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55914642	AGGAATCCAGATAAC[A/G]GAATGGCCATAGTGG	4067
rs144848311	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55987773	GCTTAAGAGCACAGA[C/T]TCTTAAGCCTGGACC	4067
rs144849234	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55989233	GCCTTTGAGAAAAGC[A/G]GGAAAGATGAATGAC	4067
rs144850165	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55944466	AACACAAGTTTTTTC[A/G]TTTTGCACTTATTTA	4067
rs144886883	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55949033	TTACCAGCTTACCTG[A/C]TTGCTTCTTCCAGTG	4067
rs144923389	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55952285	ATAGTTAGGCCAGGC[A/G]CAGTGGCTCACGCCT	4067
rs144938693	snp	C/T	0.00953873	0.0683987	intron-variant	LYN	GRCh38.p7	8:55946627	TTACCCTCTTAACTA[C/T]TTTTAAGTATACATT	4067
rs144981718	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55934307	AGCTTAAGTTTGCCA[A/G]CAGGGTTTGAATCTT	4067
rs144991165	snp	A/G	0.0287284	0.116357	intron-variant	LYN	GRCh38.p7	8:55896808	CAGTGGCGTGATCTC[A/G]GCTCCCCGCAACCTC	4067
rs145011760	in-del	-/AAAAAAAA/AAAAAAAAAT/AAAAAAAT			intron-variant	LYN	GRCh38.p7	8:56008123	ACTCTGCCTCAAAAA[-/AAAAAAAA/AAAAAAAAAT/AAAAAAAT]AAAAATAAAATAAAA	4067
rs145039039	snp	G/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55957905	GTGAGCTGAGATTGC[G/T]CCGCTGTCACCAAAC	4067
rs145056050	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55884912	GAATTAGCTGGCAGC[A/G]TTCCTTATTTGCCAC	4067
rs145145640	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55973701	CAAGTGAATCAAAGC[A/G]TTTATTACTCTTTGG	4067
rs145166126	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55930037	GGGCGTGAACCCCAT[C/T]GTGAACTGCACATGT	4067
rs145193335	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55912219	GTGTAACACATTTCT[C/G]TGTGCCCCTTTTGCA	4067
rs145206611	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56002021	CACGGCAGCTCACAC[A/G]TGTAATCCTAGCACT	4067
rs145218552	snp	A/G	0.000153988	0.00877328	missense	LYN	GRCh38.p7	8:55946490	CAGAGGTTTCAAACT[A/G]AAGGTATGTTTTCAT	4067
rs145242961	snp	C/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55989068	GTTCTCTGGTGGTAG[C/G]AGCCGGGTATGTGTG	4067
rs145259997	snp	C/T	0.00398564	0.0444627	intron-variant	LYN	GRCh38.p7	8:55971211	AAGGAAAGGACCCAG[C/T]AGCCCTGCCTTTTTA	4067
rs145263129	snp	C/T	0.00318978	0.0398085	intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55923353	CATCTGCTCAGTTTC[C/T]GCCTCTCTGTCAAGC	4067
rs145308895	snp	G/T	0.0471551	0.14613	intron-variant	LYN	GRCh38.p7	8:55927772	ACCTGGGAGGCAGAG[G/T]TTACAGTGAGCCAAG	4067
rs145429061	snp	A/G	0.00438332	0.0466095	intron-variant	LYN	GRCh38.p7	8:55944314	CAGATATAGAACCAT[A/G]TCATATATAAATATG	4067
rs145448944	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55949173	GTGTCCATCTCTATG[A/G]TAACTAGATGTTTGA	4067
rs145492121	snp	C/T	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55988559	TCAAGCATAGGAAGA[C/T]AATACATCCTTAGAG	4067
rs145497179	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55888950	ACACTGGCTTTTTGT[A/G]TTATTTCAAATTTGA	4067
rs145538987	snp	G/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55947957	TTCCCTTTGAAGACA[G/T]ACAGTGGTTTTTCTT	4067
rs145587944	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55951510	TTTCTATAAGAAATT[A/T]AAAAATTAGCCAGCT	4067
rs145595665	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55917926	ATGTTGTATTCATAG[A/T]AGTTCTTTGGGTTTC	4067
rs145595693	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55993459	TACTGAGCTCTCTTG[A/G]TACTGAGCTCTCTTG	4067
rs145613336	snp	C/T	0.00318978	0.0398085	intron-variant	LYN	GRCh38.p7	8:55897960	GATTAGTAAGCAATT[C/T]TTTTCTTTGGAAAAA	4067
rs145631745	snp	C/T	0.0126979	0.078662	intron-variant	LYN	GRCh38.p7	8:55972689	ACTAATTAAATCTAT[C/T]ACTTTTCCATAGTGC	4067
rs145665634	snp	A/C	9.98585e-05	0.00706536	missense	LYN	GRCh38.p7	8:55946456	CTCGTAGGTTCCAGA[A/C]TCTCAGCTTTTACCT	4067
rs145683565	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55907252	TGGGGTATTACTCAA[C/T]CAAAAAAATGAGACA	4067
rs145802087	snp	C/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55941087	ATGAAAGCCAGGCCA[C/T]CTTCCTAGGCCCCTA	4067
rs145841815	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, downstream-variant-500B	LYN	GRCh38.p7	8:56011899	AGAACCACAAGTATT[A/G]CCCAATATGTTACAT	4067
rs145861052	snp	A/T	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:56005725	GGAGGAGGCAAAAGA[A/T]CTTTACTTCATTATC	4067
rs145868845	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55904092	TGTAAAAAATGTGTT[A/C]TCTGAAAGTTGATAA	4067
rs145890982	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55980529	CAGGCATACACCATC[A/G]TGCCCCACAGTTGCT	4067
rs145891957	snp	C/T	0.00597247	0.0543191	intron-variant	LYN	GRCh38.p7	8:55899145	GTTTTACTTTTGTAT[C/T]AGGCAATAATTACCT	4067
rs145892018	snp	A/C	0.00319106	0.0398404	intron-variant	LYN	GRCh38.p7	8:55944583	CCTCCTGAGTTCAAG[A/C]GATTCTCCTGCCTCA	4067
rs145896571	snp	C/T	0.00597247	0.0543191	intron-variant	LYN	GRCh38.p7	8:55968659	AGCCTGAGGGCTAAG[C/T]ACTATTGTTCTGTGT	4067
rs145903042	snp	A/C	0.00676609	0.0577691	intron-variant	LYN	GRCh38.p7	8:55894476	CTGGGCTCCAGGGAT[A/C]CTCCCACCTTAGCCT	4067
rs145910133	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55885061	TCTTCTGCTCTCCCC[A/G]CTTCATTCCCTATCA	4067
rs145955615	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55995550	TGTTCCTGCAGAAAT[C/T]GTGGACAGGTAGTCA	4067
rs145957127	in-del	-/A	0.0228947	0.104514	intron-variant	LYN	GRCh38.p7	8:55985604	CACATCAAGTTCTTT[-/A]AGGTATTTTGTCTTA	4067
rs145958484	snp	A/G	0.00398564	0.0444627	intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55922888	GGATGGTTAGACGTA[A/G]CAGGGCTGTTGTAGC	4067
rs145978065	snp	A/C	0.000626329	0.0176854	synonymous-codon	LYN	GRCh38.p7	8:55951967	TTTTCCCCCCATAGG[A/C]AGCTTCTCTCTGTCT	4067
rs145993833	snp	A/G	0.0498117	0.149749	intron-variant	LYN	GRCh38.p7	8:55943469	TAGTCCCAGCTACTT[A/G]GGAGGCTGAGGAAGA	4067
rs146006739	in-del	-/ATATATATATATACACACACACACACAC			intron-variant	LYN	GRCh38.p7	8:55908999	TGTATGTATATATAT[-/ATATATATATATACACACACACACACAC]ACACACACACACACA	4067
rs146037177	snp	A/G	0.0123036	0.0774623	intron-variant	LYN	GRCh38.p7	8:55890000	CAAGTTGCTTAGCTG[A/G]GTGAAGTGGCTCATG	4067
rs146078280	snp	A/C	0.00517822	0.0506191	intron-variant	LYN	GRCh38.p7	8:55979716	AGCACAGCTCTGCAG[A/C]TCTCACCCTGATTCA	4067
rs146104818	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55983067	CACCTATTTTGCCCT[C/T]ATGTCCACACAACAG	4067
rs146175990	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55905423	TCAAAAAAAAAGAAA[A/G]AAAGAAAGAAAGAAA	4067
rs146203606	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55962410	CCCTATGATGTTGGT[A/G]AGATGCATCCGTGCT	4067
rs146251736	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55905687	CAAACACTTAAGAGG[C/G]CTATGGGATGGGCAG	4067
rs146335545	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55945758	AATAACAGGGGATGC[C/T]ATCTGTCCCTGTGAT	4067
rs146337916	in-del	-/A	0.0142736	0.0832652	intron-variant	LYN	GRCh38.p7	8:55880286	GGCGAAGGCTCTTAG[-/A]TGTCTTCAGCCGACG	4067
rs146360725	snp	A/G	0.0217236	0.101931	intron-variant	LYN	GRCh38.p7	8:55887830	GGCCAGGCTGGTCTC[A/G]AACTTCTGGCCTCAA	4067
rs146383670	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55965065	TCCAAGAGAAAGATG[G/T]AAGCAGAAGAGAGGA	4067
rs146415366	snp	A/C	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55916767	CTGCAATGGCACCTT[A/C]GGCTGTGTGTGTGTC	4067
rs146443249	snp	C/T	0.00874735	0.0655527	upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55879360	GCCCTGAACAGCCTC[C/T]TGTACACCCTTAAGG	4067
rs146454168	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55883839	ATAATGAAGAGAAGA[A/C]CATGGAAGAGGAAGT	4067
rs146476144	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55994144	AACAAATTAAGGTTT[C/T]AAAAAAAATAAACCA	4067
rs146525493	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55989072	TCTGGTGGTAGCAGC[C/T]GGGTATGTGTGCTGA	4067
rs146532559	snp	G/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55912416	GCTTAAGTAGTTTTT[G/T]AAATTTTAACCCAAA	4067
rs146552479	snp	A/G	0.00478085	0.0486577	intron-variant	LYN	GRCh38.p7	8:55976860	GTATATGGAGAGAAC[A/G]GCTTAGGGGGCACTC	4067
rs146572080	snp	A/G	0.00755907	0.0610114	intron-variant	LYN	GRCh38.p7	8:55998094	GTCTCAAGAAAAAAA[A/G]AGAAAATGTTAAGAC	4067
rs146582033	snp	C/T	0.00636936	0.0560724	intron-variant	LYN	GRCh38.p7	8:55924183	TGAGTGAGTACCTCT[C/T]ACGATGTGTGAGAGA	4067
rs146582157	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55882874	TTTTGGCTCTTTCTA[C/T]TTGTCCACCTTTGGA	4067
rs146590426	snp	G/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55937116	TCCATAGTCCTTACT[G/T]CAGAATATGTTGTGA	4067
rs146623587	snp	C/T	0.00557542	0.0525036	utr-variant-3-prime	LYN	GRCh38.p7	8:56010444	GTTTACAAATGGACA[C/T]AGGACTCAAAGTTTC	4067
rs146648414	snp	C/T	0.00318978	0.0398085	intron-variant	LYN	GRCh38.p7	8:55972742	ATTAAAGCTGCCCCA[C/T]GGTGACAGAGATCCC	4067
rs146649403	snp	G/T	0.00835141	0.0640778	intron-variant	LYN	GRCh38.p7	8:55898222	TTGTGTTTTCTGTAA[G/T]GTCATATAAATAGAT	4067
rs146660177	snp	C/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55957708	GGCACTTCGGGAGGC[C/T]GAGGCAGGTAGATCA	4067
rs146685499	snp	C/T	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:55912048	TAGTGTTTCCCTGCT[C/T]AAATGGAAGGAGAGA	4067
rs146696606	snp	C/T	0.00517822	0.0506191	intron-variant	LYN	GRCh38.p7	8:55915268	TGTGAACATACACAC[C/T]GCAATTCCAGATACC	4067
rs146770592	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55953000	TCTATGACCTGCTCG[A/G]AGGGGATGCACATTA	4067
rs146780339	snp	C/T	0.00755907	0.0610114	intron-variant	LYN	GRCh38.p7	8:55937943	CTCAGATGATCCACC[C/T]GCCTCGGCCTCCCAA	4067
rs146791536	snp	A/G	1.648e-05	0.0028705	missense	LYN	GRCh38.p7	8:56009980	TGGAGAACTGCCCAG[A/G]TGAGCTCTATGACAT	4067
rs146806354	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55897349	TCATAATAATAAGCT[A/G]CATGCTTCTGGAAGT	4067
rs146848077	snp	A/G	8.26248e-05	0.00642694	synonymous-codon	LYN	GRCh38.p7	8:55998354	TTTTCAGATTGCAGA[A/G]GGAATGGCATACATC	4067
rs146856428	snp	C/T			intron-variant	LYN	GRCh38.p7	8:56003928	ATTAAATATTTTATT[C/T]TTTTTTTTTTTTTTT	4067
rs146886785	snp	A/C	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:56005366	CCACTTGGGCCTAGC[A/C]TTCCCTGCATGAAGC	4067
rs146889838	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55935040	CGGAAGCAGCTCCAC[A/G]GGCCATGGTCATAGC	4067
rs146927263	in-del	-/AA/AAATAA	0.499234	0.0195537	intron-variant	LYN	GRCh38.p7	8:55887559	TATAAAAATATAAAT[-/AA/AAATAA]ATATATATATATATA	4067
rs146937883	snp	A/G	0.245346	0.249957	intron-variant	LYN	GRCh38.p7	8:55902251	AACCTCAGGTGATCT[A/G]CCCATTTTTGCCTCC	4067
rs146943216	in-del	-/A			intron-variant	LYN	GRCh38.p7	8:55951247	GTGAGGCACTGTCTC[-/A]AAAAAAAAAGAGAAA	4067
rs146948177	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55977882	TATGATTACACCCAC[C/T]GCCCTCCAGCCTAGG	4067
rs146958078	snp	G/T	0.00795532	0.062565	intron-variant	LYN	GRCh38.p7	8:55981510	GAAGAACATATTTTT[G/T]GTGTGTTTAAAAAAA	4067
rs146982629	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55917978	GCTTAAGCAGAAATG[A/G]GGGATTTATTGGAAG	4067
rs147053791	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55959465	TGCAGGTAAGTTCAA[C/T]TGACAGCATTCAAAG	4067
rs147063313	snp	A/T	0.00914312	0.0669923	intron-variant	LYN	GRCh38.p7	8:55963187	CATTTTTGTGCCTCA[A/T]TTTTGTGCTGATGCA	4067
rs147064165	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55912810	ATAAGCACAGTTACA[A/G]TATTATATTTCCTGA	4067
rs147076806	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55901995	ATGTATCATCATTCT[A/G]AAAAACGTACCTGTA	4067
rs147136759	snp	C/T	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:56006562	CTGATTTCTACCCAC[C/T]CCAGATGCCACCTTC	4067
rs147137791	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55891681	TACTTAAAATAGTTA[C/T]GATACAAGTTTTATA	4067
rs147138204	snp	A/G	0.00755907	0.0610114	intron-variant	LYN	GRCh38.p7	8:55935643	GCCATGCTTGGTGGC[A/G]GACGCCTGTAGTCCC	4067
rs147148234	snp	A/G	0.021333	0.101051	intron-variant	LYN	GRCh38.p7	8:55895556	GCACTTGGGGAGGCC[A/G]AGGCAGGAGGATCAC	4067
rs147149362	in-del	-/G			intron-variant	LYN	GRCh38.p7	8:55939533	CTGCAGGAACGCAGT[-/G]GGGGGGGGGACAGGG	4067
rs147182525	in-del	-/AATATGATATGA	0.149999	0.229128	intron-variant	LYN	GRCh38.p7	8:55904332	AAATAAATTTCTTAG[-/AATATGATATGA]AATATGATATGAAAT	4067
rs147220013	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55933376	CTATAATTTGACAAA[C/T]AAGCCTATTTCTATA	4067
rs147231822	snp	A/G	0.00517822	0.0506191	intron-variant	LYN	GRCh38.p7	8:56003582	CTGAGGCAGAGAATC[A/G]CTTGAATGCTTGAAC	4067
rs147238869	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55990695	AGTCTCAGGATCTCT[A/G]TTTTAATGTGAATGC	4067
rs147242973	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55913983	GACTTGCTAAGCTCT[A/G]TCAGATGAGCAATGA	4067
rs147252724	snp	C/T	0	0	upstream-variant-2KB	LYN	GRCh38.p7	8:55877296	GTGGGGGGGGTCTCA[C/T]GATATTGCCTAGGAT	4067
rs147326316	snp	C/T	0.0142736	0.0832652	intron-variant	LYN	GRCh38.p7	8:55911411	ACGGGCGTGAGCCAC[C/T]GCACCCAACCGGTTT	4067
rs147347615	in-del	-/A			intron-variant	LYN	GRCh38.p7	8:55890118	CTGCCTCTATAGACA[-/A]AAAAAAAAAAAAAAA	4067
rs147349225	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55899371	GTTTGTTTTATTTAA[C/T]TTTGAAAGGTTATTT	4067
rs147376208	snp	C/T	4.96077e-05	0.0049801	synonymous-codon	LYN	GRCh38.p7	8:55952093	TTTTCCCTGTATCAG[C/T]GACATGATTAAACAT	4067
rs147377031	in-del	-/TAATTT	0.02016	0.0983543	intron-variant	LYN	GRCh38.p7	8:55908912	TTGCTGCAAAATACA[-/TAATTT]TATTCTTTTTTATGG	4067
rs147419017	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56007143	CATTCTGACCTTTTA[G/T]GCAAATGAGGGATCT	4067
rs147434289	snp	A/T	0.00398564	0.0444627	intron-variant	LYN	GRCh38.p7	8:55896071	TTTATCATTAGCTCA[A/T]CCTTAAGCATCTCGT	4067
rs147442120	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	LYN	GRCh38.p7	8:56012401	TTAGCTGTTGTGCAG[C/T]GGGAGATGTATGTCA	4067
rs147442160	snp	C/G	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:55970327	GCCTAGGAGTTGCCT[C/G]TTTATTTACTTTGGA	4067
rs147443978	in-del	-/G/GG	0.108846	0.206649	intron-variant	LYN	GRCh38.p7	8:55919917	TTGGGCGGGGGGAGT[-/G/GG]GGGGGTGGGAGCTTT	4067
rs147452257	snp	A/C	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55954496	GCAGCAAGATTATAG[A/C]AGTGGCTTTTTCCAG	4067
rs147524725	snp	C/T	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:55991600	TTCACCAGAACCCCC[C/T]ACCCCCAGGATTTGC	4067
rs147538800	snp	A/G	0.00438332	0.0466095	upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55878752	TCACAGGTATAAACC[A/G]CCTTTCTTCTTTTAA	4067
rs147547214	snp	C/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55994704	TTGGGACTTCAGCCA[C/G]CTTTGGCTTCTTTGG	4067
rs147547470	snp	C/T	0.000875606	0.0209054	synonymous-codon	LYN	GRCh38.p7	8:55950744	GGCACCAGGAAATAG[C/T]GCTGGAGCTTTCCTT	4067
rs147600014	in-del	-/CA			intron-variant	LYN	GRCh38.p7	8:55909054	CACACACACACACCC[-/CA]CACATTTTCTTTACT	4067
rs147600256	snp	A/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55984793	CGGAATGCAGGGGGA[A/T]GCCCCCATAAGGCCA	4067
rs147609093	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55923834	GTGAGCCACCGCGCC[C/T]GGCCAAGATCAAACA	4067
rs147705881	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55967785	TTTTCTTCTACTGTG[A/T]TCACCTTCATATACA	4067
rs147733188	snp	A/G	0.00358779	0.0422022	intron-variant	LYN	GRCh38.p7	8:55984322	GCCCAAACTGCTCCC[A/G]TGAGCCCCTGCTGGC	4067
rs147735883	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55907417	AGGGTCATGAGAGGG[G/T]ATGCCTTAGAAAGGA	4067
rs147820661	snp	C/G	0.00438332	0.0466095	intron-variant	LYN	GRCh38.p7	8:55890278	GATTACACCACCACA[C/G]TCCATCCTGGGTGAC	4067
rs147843347	snp	A/C	0.0693013	0.172766	intron-variant	LYN	GRCh38.p7	8:55892203	CGAGGCAGATGGATC[A/C]CGAGGTCAGGAGTTC	4067
rs147890552	in-del	-/TTTA	0.0383715	0.133092	intron-variant	LYN	GRCh38.p7	8:56004779	ATATGGCCACATACT[-/TTTA]TTTTTCATTTATTTA	4067
rs147901326	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55998583	AAAGCAATTACAATA[A/G]TCACCATTAAGAAAA	4067
rs147911577	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56001516	GTTGGCAGCTGAAAG[C/G]CTTTGGGTGGTGTCT	4067
rs147925414	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55944527	CTCTTGTTGCCCAGG[A/C]TGGAGTGCAATGGCA	4067
rs147925463	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55987859	ACTCAGCTTCGTCCT[C/T]GTTACTATGAATATA	4067
rs147948603	snp	C/T	0.00676609	0.0577691	intron-variant	LYN	GRCh38.p7	8:55946657	TTCAGCAGCATTAGG[C/T]ACATTCACATTGTTG	4067
rs148007223	snp	A/G	0.0228947	0.104514	intron-variant	LYN	GRCh38.p7	8:56006118	CTTGTTGGGGTCCTG[A/G]TTGGGGTCTTGTTTT	4067
rs148017481	snp	A/G	1.64741e-05	0.00286998	intron-variant	LYN	GRCh38.p7	8:55969810	TAACATATTCAAAAA[A/G]CCCCGTGTGCACGTG	4067
rs148018491	snp	C/G	0.0693013	0.172766	intron-variant	LYN	GRCh38.p7	8:55895021	ATCTCACTATGTTGC[C/G]CAGGCTGGTCTTGAA	4067
rs148037837	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55953327	TGCTGAAGAATACAA[C/T]CAAGTATGTTTTAAA	4067
rs148058565	snp	A/G	0.00279162	0.0372561	intron-variant	LYN	GRCh38.p7	8:55943176	ATCTACTTCATTTCC[A/G]AGCTTATATCCTTTG	4067
rs148059167	snp	A/G	0.00199481	0.0315187	downstream-variant-500B	LYN	GRCh38.p7	8:56012572	AAAATTTTAAAAATT[A/G]GCTAAGTGTGGTGGC	4067
rs148167023	in-del	-/AAAT			upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55878808	TCTTTTCCTAGTAAC[-/AAAT]AACTGCTGTATCAGA	4067
rs148176246	snp	C/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55999301	TTCCAGCCTGGGTGA[C/T]AAGAGTGAAACTCCG	4067
rs148178471	snp	C/T	0.0209421	0.100162	intron-variant	LYN	GRCh38.p7	8:55924927	GCTCACTGCAGCCTC[C/T]GCCTCCCAGGTTCAA	4067
rs148218082	snp	A/G	0.0023933	0.0345097	intron-variant	LYN	GRCh38.p7	8:55975023	TACACATTCCCAATC[A/G]CTCTTTCAAGCACAA	4067
rs148229038	snp	A/T	0.0023933	0.0345097	intron-variant	LYN	GRCh38.p7	8:55932010	TCCAACACATATGAC[A/T]TGCTTAAACTTTAGT	4067
rs148251602	snp	C/T	0.0685596	0.171987	intron-variant	LYN	GRCh38.p7	8:55912554	AACGTGGCGAAACCC[C/T]GTAGCTACTAAAAAT	4067
rs148252653	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55989317	TTGGATTTGTAAAAC[A/G]TAATTGAGATTGTGC	4067
rs148289584	in-del	-/AAATAAAT			intron-variant	LYN	GRCh38.p7	8:55954836	TGAGACCCTGCCTCA[-/AAATAAAT]AAATAAATAAATAAA	4067
rs148304843	snp	A/C	0.0103295	0.0711199	intron-variant	LYN	GRCh38.p7	8:55919011	CGAGACCATGGGAGA[A/C]CCTGTCTCTACAAAA	4067
rs148383979	snp	A/G	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:55964206	TAACACTTATCTTGT[A/G]CTGCATTTTTCTTTT	4067
rs148406773	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55889039	TTTGTATGTTTTGAG[A/T]TGGGGTCTCACTCTG	4067
rs148490398	snp	A/T	0.00716266	0.059414	intron-variant	LYN	GRCh38.p7	8:55899440	CCTTGACTTTAGTTT[A/T]TCAAGCAGACTTTAT	4067
rs148508434	snp	C/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55987385	ACACTCCAGCTTGGG[C/G]TACAGAGTGAGACTT	4067
rs148531538	snp	C/T	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:55945761	AACAGGGGATGCCAT[C/T]TGTCCCTGTGATGGA	4067
rs148562868	snp	C/G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55991985	GACATCGTCTCTTTA[C/G/T]GTGATTAGTCTCATT	4067
rs148564241	snp	A/T	0.00597247	0.0543191	intron-variant	LYN	GRCh38.p7	8:55915110	TGTGTTAAAGCCTTA[A/T]CTATTATCTGCTCTT	4067
rs148573787	snp	A/C			upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55878767	ACCTTTCTTCTTTTA[A/C]GGAATTAGTATGCAA	4067
rs148613586	snp	A/G	0.00993419	0.0697739	intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55922891	TGGTTAGACGTAGCA[A/G]GGCTGTTGTAGCAAT	4067
rs148654954	snp	A/G	0.00676609	0.0577691	intron-variant	LYN	GRCh38.p7	8:55971386	TCAGGAAATGGAGAA[A/G]GCAGAAGTCTGATAA	4067
rs148722355	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55950135	TGAGTAATACTCCAC[C/T]GGATGGATATTCCAG	4067
rs148732118	snp	G/T	0.0103295	0.0711199	intron-variant	LYN	GRCh38.p7	8:55906487	TCAGCCTCCCAAGTA[G/T]CTGGGATTACATGTG	4067
rs148737723	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56009722	CAATTCTGAGGTGTA[C/T]GCGGGGTTAGGACTT	4067
rs148761348	snp	C/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55995292	GACTTCCCATCAAGG[C/G]TGTTTGAATCTTTTC	4067
rs148771402	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55956723	TCTATTCCAACCCCA[C/T]TGGCTCACGTCAAGA	4067
rs148776915	snp	C/T	0.00318978	0.0398085	intron-variant	LYN	GRCh38.p7	8:55883725	AGGGCTCATAGGACG[C/T]ACATTAAAACACCTG	4067
rs148835627	snp	A/G	0.00636936	0.0560724	intron-variant	LYN	GRCh38.p7	8:55988895	GAAAAAAAAAAACCC[A/G]AAAAACAAAAAACTC	4067
rs148845334	snp	C/T	0.00358779	0.0422022	intron-variant	LYN	GRCh38.p7	8:55948031	CAGGCTAGAATGCAG[C/T]GGCATGATCATAGCT	4067
rs148877182	snp	G/T	0.00318978	0.0398085	intron-variant	LYN	GRCh38.p7	8:55917963	AACCTCCTCTTGCTA[G/T]CTTAAGCAGAAATGG	4067
rs148887503	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55993646	ACCTGGTCAATTTGC[C/T]ATTAAGATGAAACAT	4067
rs148900408	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55881235	AAGCTAAGACTACCA[A/T]GTCAGATTTAGCCAT	4067
rs148921396	snp	C/T	0.00597247	0.0543191	intron-variant	LYN	GRCh38.p7	8:55968538	CTGGAATTATAGGTG[C/T]GAGCCACCAAGCTTG	4067
rs148921562	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55938109	TTGAATGAGGATGAG[C/T]CACCCCTAATGGATA	4067
rs148963886	in-del	-/T	0.0444908	0.142359	intron-variant	LYN	GRCh38.p7	8:55951754	CATGAAGAAAGAAAA[-/T]TGGTATGTTGGCAAG	4067
rs149001790	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55981128	TTCCCTATCCCAGTG[C/T]CTCTCCAGAGCCCAC	4067
rs149053008	snp	A/G	0.00318978	0.0398085	intron-variant	LYN	GRCh38.p7	8:55985113	CTTTTTCTAGGTCAC[A/G]CATCTTGCAAGGGAA	4067
rs149056610	snp	C/T	0.0142736	0.0832652	intron-variant	LYN	GRCh38.p7	8:55908359	GAGTGATTCTCCTGC[C/T]GTGGCCTCCCAAGTA	4067
rs149064199	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	LYN	GRCh38.p7	8:56011406	TTTTATTTGCATTTA[C/T]ATTTTCAGCTGTGGT	4067
rs149087421	snp	A/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55958138	TGTTCTGTCGTAAGG[A/T]GTAAGTCTGCACTAA	4067
rs149110101	snp	A/T	0.00279162	0.0372561	intron-variant	LYN	GRCh38.p7	8:55912530	CAGGAGTTCGAGACC[A/T]GCCTGGCCAACGTGG	4067
rs149124872	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55960552	ATACAACCAAAAGAG[C/T]TGTGATTGGTGATTT	4067
rs149135061	snp	G/T	0.000153988	0.00877328	missense	LYN	GRCh38.p7	8:55947709	GAAAGGAGAGAAGAT[G/T]AAAGTCCTGGAGGAG	4067
rs149138666	snp	A/C	0.0275645	0.114116	intron-variant	LYN	GRCh38.p7	8:55890919	TTTTTTGTAGAGATA[A/C]GGTTTTGCCATGTTG	4067
rs149149357	snp	A/C	0.00279162	0.0372561	intron-variant	LYN	GRCh38.p7	8:55963638	AGTGGTTTCTCATGA[A/C]TTTATTTGCATTTCT	4067
rs149171754	snp	G/T	0.0955749	0.196603	intron-variant	LYN	GRCh38.p7	8:55896816	TGATCTCGGCTCCCC[G/T]CAACCTCTGCCTTCC	4067
rs149226238	snp	C/T	0.00358779	0.0422022	intron-variant	LYN	GRCh38.p7	8:55901535	GGTGGTTTCCCTGGA[C/T]TTAGTATCCCCCAAA	4067
rs149308155	in-del	-/CTT	0.0232847	0.105357	intron-variant	LYN	GRCh38.p7	8:55985176	TGGGGAGGAACTGTA[-/CTT]CTCTCACTGCTCTAA	4067
rs149319281	snp	C/T	0.00279162	0.0372561	intron-variant	LYN	GRCh38.p7	8:55982493	TTACAAGGAGCTGTA[C/T]GGCTTGATCTTCTTT	4067
rs149381655	snp	A/G	0.00517822	0.0506191	intron-variant	LYN	GRCh38.p7	8:55986363	CTGGGTTTTGATAAT[A/G]TCTATCTTCGGGGTA	4067
rs149391898	snp	A/C	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55974672	ATATTTGCCAATATC[A/C]TCCAAAGTGGGTCTC	4067
rs149396873	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55899013	TTATTTTTTGTAAGG[A/T]TGAGGTCTCCATATA	4067
rs149416427	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55960818	GAAATGCAGTGAACA[A/G]ATACTAGGAAGTGAC	4067
rs149425228	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55914447	GCACTTATTTGCTCA[C/T]GTGAGCCGTGTACAG	4067
rs149455630	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56003407	CTATACAGGCCAGGT[C/G]TGGTGGCTCATGCCT	4067
rs149484397	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55975828	TTGGTAAGGTGGGGG[G/T]GGGGCTGTTTTGCAT	4067
rs149532747	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55944998	AGATGCCCTCCACTC[A/G]TGAGCCAGTTAGCCT	4067
rs149548101	in-del	-/T			utr-variant-3-prime, downstream-variant-500B	LYN	GRCh38.p7	8:56011974	GAAAATGACTAGAGG[-/T]TTTTTTTTTAGCATA	4067
rs149574097	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55990369	AGCAAAGGTTCTTAT[C/T]ATGTAGATGAAGACT	4067
rs149584056	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55950044	GTCCTTTTTGACTGC[C/T]TTCTTTTATTTAGCA	4067
rs149584456	snp	A/G	0.00993419	0.0697739	upstream-variant-2KB	LYN	GRCh38.p7	8:55876927	GCTCTTGTATGCTGC[A/G]TCCCATTATTTGTGG	4067
rs149605729	snp	A/G	0.00676609	0.0577691	intron-variant	LYN	GRCh38.p7	8:55935144	TAATTGCCCCCAAAC[A/G]CTGTTCCTATTACAC	4067
rs149637122	snp	C/T	0.00835141	0.0640778	intron-variant	LYN	GRCh38.p7	8:55883594	TACCTGAGTAATACT[C/T]TGCAAAAGGACTTTC	4067
rs149694086	snp	C/G	0.00795532	0.062565	intron-variant	LYN	GRCh38.p7	8:55988289	CTTTTTGCAAACTCC[C/G]TGGTGTGTGTGTGTG	4067
rs149698869	snp	A/G	0.00279162	0.0372561	intron-variant	LYN	GRCh38.p7	8:55911994	GTCGTGGTGTGTTCT[A/G]CCACGTCCCTTCTAG	4067
rs149707992	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55976055	AGTCACAAAATGCTA[C/T]TCTCTTTGGGTACTC	4067
rs149728906	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55962676	TGTTTTCAAGATATA[C/T]GATCATTTATCCATT	4067
rs149761954	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55903946	GATCCGCTTGAGCCT[C/T]GGAGGTTGCAGCTGC	4067
rs149769712	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55979880	GCCGCCCACCCTGGT[A/G]CGGAAGACCCCACCC	4067
rs149770859	snp	C/T	0.0150606	0.0854603	intron-variant	LYN	GRCh38.p7	8:56005075	AGGTGTGAGCCACCA[C/T]GCCCGGCCAGCCACA	4067
rs149812274	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55907891	GTAAGTAGTTTAAAT[A/C]AATAAATAAATACAA	4067
rs149886577	snp	A/G	1.7232e-05	0.00293525	intron-variant	LYN	GRCh38.p7	8:55966937	CTTGCAAGGGCTTCA[A/G]ACTCAAAAAGTAAAA	4067
rs149910855	snp	A/G	0.00279162	0.0372561	intron-variant	LYN	GRCh38.p7	8:55952213	AACTTTTTATGCATC[A/G]TATTTCTCTTAGATA	4067
rs149928989	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56009628	AGGATACTAGTCATA[C/T]TGGATTAAGACCTAC	4067
rs149939350	snp	A/G	0.0107246	0.0724382	intron-variant	LYN	GRCh38.p7	8:55996982	AAAAACTAGCATGGT[A/G]AAACCCCGTCTGTAC	4067
rs149941403	snp	C/T	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:55896560	ACCTAATGTAGATGA[C/T]GGGATGGTGGGTACA	4067
rs149962542	snp	C/T	0.0693013	0.172766	intron-variant	LYN	GRCh38.p7	8:55957862	TTGAGGTGGGAGGAT[C/T]GCTTGAGCCTAGGAG	4067
rs149972774	snp	C/T	0.0711525	0.174681	intron-variant	LYN	GRCh38.p7	8:55944045	AGTGAGCCGAGATCA[C/T]GCCACTGCACTCCAG	4067
rs150043942	in-del	-/TGC	0.0126979	0.078662	intron-variant	LYN	GRCh38.p7	8:56000418	TTTTTCCATGGTCTG[-/TGC]TGCTGGCATGGTTAA	4067
rs150067081	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55984301	CACTCCGAAGCTTCT[A/T]GCTCAGCCCAAACTG	4067
rs150086163	snp	C/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55982199	TCTGGCAATGTTATA[C/T]GTTACAGAGCCAACT	4067
rs150170597	snp	A/G	0.0154538	0.0865337	intron-variant	LYN	GRCh38.p7	8:55917298	TCATGTGATCGTCCC[A/G]CCTCAGCCTCCCAAG	4067
rs150197767	snp	A/G	3.29576e-05	0.00405928	missense	LYN	GRCh38.p7	8:56010005	TGACATTATGAAAAT[A/G]TGCTGGAAAGAAAAG	4067
rs150201442	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55893520	TGTTATTTCAACTTC[C/T]GTTTCATGTAGTTTT	4067
rs150240132	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	LYN	GRCh38.p7	8:56010709	AAACATTTTTCTTCT[A/G]TGAACACTGCTCAGA	4067
rs150242542	snp	C/G	0.0023933	0.0345097	intron-variant	LYN	GRCh38.p7	8:55939080	CTCAGTTTTTGTCAG[C/G]AGTATATTGTATTTT	4067
rs150367348	in-del	-/T	0.0158469	0.0875917	utr-variant-3-prime	LYN	GRCh38.p7	8:56010657	CCCAGATTTCAATGA[-/T]TTTTTTCCCCCTACC	4067
rs150379630	snp	C/T	0.00517822	0.0506191	intron-variant	LYN	GRCh38.p7	8:55985542	GTCAGGGATTGTTTT[C/T]GGAGCCCAGGCGCTG	4067
rs150381734	snp	G/T	0.0111196	0.0737302	intron-variant	LYN	GRCh38.p7	8:55884903	CTCATTACTGAATTA[G/T]CTGGCAGCATTCCTT	4067
rs150420035	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:56001875	GGTGATTGGGCCCCT[C/T]GCTGGTGGCAAAGCT	4067
rs150431670	snp	C/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55989594	AACTTGGACTTTCTA[C/G]TTTAACATTGTTAGA	4067
rs150435582	snp	C/G	0.00636936	0.0560724	intron-variant	LYN	GRCh38.p7	8:55890372	TACTATAAAAAATGA[C/G]AAATCATGATGAAAT	4067
rs150455605	snp	C/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55977231	ACCGGTTCATTCTCA[C/G]TTGTGGAAGACTAAA	4067
rs150463456	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55935108	ATCTGAGGGATTCCC[A/G]GCACCGAAACAGCAT	4067
rs150529168	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55969935	GAAAAAGACCTTCCA[C/T]AATACAATTCTTGGA	4067
rs150536509	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55927265	CTCTATTCCCGAAAC[C/T]TCTGGCAACCACTGA	4067
rs150557999	snp	C/G	0.00795532	0.062565	downstream-variant-500B	LYN	GRCh38.p7	8:56012786	CTCAGTCTTGAGAGT[C/G]ACCATTTGGTTTGAC	4067
rs150562183	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55910260	CCCTAGATTTTCTTC[C/T]AGTATTTTTATGCTT	4067
rs150581197	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55975520	GATTCTGAGGCTATG[A/C]AGATGACATTGATAT	4067
rs150581292	snp	C/T	0.00478085	0.0486577	intron-variant	LYN	GRCh38.p7	8:55900125	CTGAAAACCAGTCAG[C/T]AAGGCCAAAACAAGA	4067
rs150608990	snp	G/T	0.0023933	0.0345097	intron-variant	LYN	GRCh38.p7	8:55946587	TTTATTTTTTTTTAT[G/T]GTGGGACATATATAA	4067
rs150633954	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55903603	TATTTTTCACTGTAA[A/G]CTCTTTCTGTTTCTA	4067
rs150676930	in-del	-/AAAAGAAAG	0.153997	0.230832	intron-variant	LYN	GRCh38.p7	8:55905415	ACTCCGTCTCAAAAA[-/AAAAGAAAG]AAAGAAAGAAAGAAA	4067
rs150694790	snp	C/T	0.00279162	0.0372561	intron-variant	LYN	GRCh38.p7	8:55886757	TGTTCTGATGCATAA[C/T]AGATATACATAGTTT	4067
rs150737107	snp	A/G	0.039522	0.134904	intron-variant	LYN	GRCh38.p7	8:56003091	TTGAGACAGAATCTC[A/G]CTCTGTTGCCCAGGC	4067
rs150737629	snp	C/T	0.0126979	0.078662	intron-variant	LYN	GRCh38.p7	8:55932577	AAGCATGCACCACCA[C/T]GCCTGGCTAATTTTT	4067
rs150747414	snp	C/T	0.00676609	0.0577691	intron-variant	LYN	GRCh38.p7	8:55891565	GAAGTTACTGCTTAA[C/T]GGGTACAGAGTTTCA	4067
rs150758299	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55992559	CCTTCTTTTGTTAAG[C/T]TGAGTTGCATCTGGA	4067
rs150770104	snp	A/G	0.0023933	0.0345097	upstream-variant-2KB	LYN	GRCh38.p7	8:55876859	GATGGCGGTGCTAAT[A/G]AAGAAGTTCCTAGAG	4067
rs150791407	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55936168	AATGATGCTTGAACC[A/G]GTCTTGGACCTAATT	4067
rs150819882	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55906890	TCCTATTGAGAATGA[G/T]TTTTCCTCTTCCTGG	4067
rs150820827	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55983831	TTCTCCACACTAAGT[C/G]TCCTAAGTGATTCCA	4067
rs150823990	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55883044	TAACCTACCTTAAAC[A/G]TGGTCGAAACACTCA	4067
rs150904137	in-del	-/TTTTG	0.296869	0.245567	intron-variant	LYN	GRCh38.p7	8:55906332	CCAAGAATTCGTTTT[-/TTTTG]TTTTGTTTTGTTTTG	4067
rs150935646	snp	A/G	0.00279162	0.0372561	intron-variant	LYN	GRCh38.p7	8:55948411	CCCAGCCTAGCTTGA[A/G]TTCTAAGGGTACTGA	4067
rs150938309	in-del	-/TGTG	0.393987	0.204372	intron-variant	LYN	GRCh38.p7	8:55909974	TTTAATGGGGTTGTT[-/TGTG]TGTGTGTGTGTGTGT	4067
rs150968226	snp	A/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55957384	GACTTTCCTATGGAT[A/T]TTTGCTGGCAAAGGA	4067
rs150997257	snp	C/T	0.00279162	0.0372561	intron-variant	LYN	GRCh38.p7	8:56001042	TGGCTTAGGGATTGG[C/T]GAGTACTCACAGAAG	4067
rs151011320	snp	A/G	0.00557542	0.0525036	intron-variant	LYN	GRCh38.p7	8:55889519	AGCCCAAGTATATTT[A/G]TCGAGTGCTGTATGT	4067
rs151020066	snp	A/G	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55962485	TTGTGAGATGCACTC[A/G]TGCTTCTGGGTGTGG	4067
rs151052738	snp	C/T	0.0383715	0.133092	intron-variant	LYN	GRCh38.p7	8:56004827	TCTTGCTCTGTCACC[C/T]GGGCTGGAGTGCAGT	4067
rs151058100	snp	C/T	8.24002e-05	0.0064182	synonymous-codon	LYN	GRCh38.p7	8:55998423	TAATGTTCTGGTCTC[C/T]GAGTCACTCATGTGC	4067
rs151086117	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55951579	TTGGGGTAGAAAGAT[C/T]GTTTGAGCCCAAGAG	4067
rs151088004	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55878856	AGCTGCTTTGACTTA[C/T]TGCTCTGTAGCTGGG	4067
rs151093800	snp	C/T	0.00835141	0.0640778	intron-variant	LYN	GRCh38.p7	8:55981438	GGATTGACTATATTC[C/T]GTTTAAAACAATAAA	4067
rs151105686	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55938228	AAAAGGCTGCCTGGC[C/T]GTTTGTGTCTCTTTA	4067
rs151138826	snp	C/G	0.00517822	0.0506191	intron-variant	LYN	GRCh38.p7	8:55884236	CTTCTGAGTAGTTGG[C/G]ATTACTTACAAGCAT	4067
rs151233851	snp	C/T	0.00438332	0.0466095	intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55923236	CTCTAAGGTACTGAT[C/T]CTTTCTGAGAGTCAG	4067
rs151234062	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55996521	CAGATAAACTACTAC[G/T]TGGCTTTCTTTACTT	4067
rs151261464	snp	A/G	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:55971646	GTATGTACTGTACCC[A/G]GAGAATGACTTTATT	4067
rs151286948	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55929309	GTGAGACTAAGTGAG[A/T]CTAAGACTTAGTGAG	4067
rs151296455	snp	A/G	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:55911754	AGGTTTTGCATGTCC[A/G]TGGAAAGGGCTTGCT	4067
rs151316186	snp	C/T	0.0402882	0.136092	intron-variant	LYN	GRCh38.p7	8:55977182	AAGAGCAAGACTCTG[C/T]CTCAAAAAAAAAATA	4067
rs151317615	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55901676	AAGAGCATTGGGCAT[A/G]CACTTCAGGAAACCC	4067
rs180752542	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55896736	CCCCAAGCTCCTCAC[A/G]TTTATTTATTTATTT	4067
rs180765338	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55915737	ATTAAGAAAAATAAG[G/T]AAATTCTCCTTACAT	4067
rs180769670	snp	C/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55935016	TGGAGGTGATGCCCA[C/T]ACCATGGACGGAAGC	4067
rs180801574	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55989234	CCTTTGAGAAAAGCG[A/G]GAAAGATGAATGACC	4067
rs180806408	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55969061	CAAGGTGGGAGGATT[G/T]CTTGAGTCCAGGAAT	4067
rs180813400	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	LYN	GRCh38.p7	8:55876673	TTGGTAGTTAGGTCT[C/G]TGGCCAAGTTGGCAA	4067
rs180813670	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55951730	TAAATAATAATTTTA[A/G]AAAAATTATCATGAA	4067
rs180816686	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55943258	CTATGGAATTCTGCA[A/G]CATTTAAGCTGGAAA	4067
rs180826716	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56005715	AAAATAGTGAGGAGG[A/G]GGCAAAAGATCTTTA	4067
rs180843787	snp	A/G	0.00279162	0.0372561	intron-variant	LYN	GRCh38.p7	8:55977731	CAGCCTGGGCAACAC[A/G]GTGAGACTCCTATCT	4067
rs180890252	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55960599	TGAAGGATACTCCCT[C/T]TCCCAATTTTGAGCT	4067
rs180891125	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55893964	GGCATGTGCCACTGC[A/T]CCTGGCTTAGAGTAT	4067
rs180896901	snp	C/T	0.00716266	0.059414	intron-variant	LYN	GRCh38.p7	8:55911483	ATACTCAAGGAATTG[C/T]GTGAACCATCTCTTT	4067
rs180912370	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55930551	TATTTCCCTACCTTA[C/T]GTAAGTTTCCATGAG	4067
rs180935864	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55984190	ATTAAATCTGGAAAG[A/T]CTCTATTTCCAAATA	4067
rs180943107	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime	LYN	GRCh38.p7	8:56010264	TCAGGAAGAACACCC[G/T]CTAAATGGGAAAGTA	4067
rs180944184	snp	G/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55881709	TAATATGCTGTGATT[G/T]GGGATAAGCCACTTG	4067
rs180945022	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55965092	AGGACAGGAAGGAAG[A/G]GTATGATTATTAATA	4067
rs180953126	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55956463	TTATCTACAGTAATC[A/C]ACCATCACTTTTATT	4067
rs180953595	snp	C/G	0.000399281	0.0141238	missense	LYN	GRCh38.p7	8:55947656	GTGGTAGCCTTGTAC[C/G]CCTATGATGGCATCC	4067
rs180962037	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55920255	GGGGGACTTGGGGAC[A/G]CATCAGACATTATCT	4067
rs180963407	snp	A/G	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55939335	ATTCGATGTTAAATT[A/G]TCCATGACAATGGTG	4067
rs180977624	snp	C/T	0.00478085	0.0486577	intron-variant	LYN	GRCh38.p7	8:56002484	AGGTGTGGTGGTGCA[C/T]GCCTGTAATCCGGAG	4067
rs180979622	snp	A/G	0.00438332	0.0466095	intron-variant	LYN	GRCh38.p7	8:55972767	GATCCCTGGGGCCCA[A/G]ATACTTCGATAATCC	4067
rs180986940	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55902776	TACTGTGATGGAAGC[A/G]TAACCTATCTCAATT	4067
rs180993118	snp	A/G/T	0.00517822	0.0506191	intron-variant	LYN	GRCh38.p7	8:55992929	CCCCCCTCTTAATAC[A/G/T]ATTGCATTGGAGATT	4067
rs181052678	snp	C/T	0.0482946	0.147699	intron-variant	LYN	GRCh38.p7	8:55910957	GCTGGAGTGCAGTGG[C/T]GCAGTCTTGGCTCAC	4067
rs181089953	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55947245	CAAGAGCGAGACTCC[A/G]TCTCAAAAGAGAAAA	4067
rs181120714	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55982806	CAATTCTGCTGCTCA[C/T]TGCTTCATTTGATCG	4067
rs181129428	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	LYN	GRCh38.p7	8:56012174	TGTGTGGAAGTCACA[C/T]GTTCCCTTGATGAAC	4067
rs181131260	snp	C/T	0.0023933	0.0345097	intron-variant	LYN	GRCh38.p7	8:55929745	CAATACACAGAACTG[C/T]CCTCTAGAACAAATA	4067
rs181133216	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55964909	CCCTAAAAAGGGGAC[C/T]GTCCACTCCACGTCA	4067
rs181139769	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55994199	GGGAAAGAATAAAGA[G/T]AATGAATTAATTTTA	4067
rs181159877	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56001811	TGTTTTGTGATATGC[A/G]TGGTGTGCTGCATGT	4067
rs181331379	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55892934	GTTGACCCTCCCCCA[A/G]GCAGTACTCCCCTGA	4067
rs181529748	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55882152	CTCTACTTATTACTG[A/G]AAGAGAGGTCCTGAT	4067
rs181534195	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55903127	GCTGGGATTACATGC[A/G]TGAGCCACTGCGCCC	4067
rs181553599	snp	C/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:56001086	GCTGGTTTTATTCCA[C/T]GGTCCTGGCAGCAGC	4067
rs181558396	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55956618	CAAATGGTTTCAGCA[C/T]GATCTGTGAATTCTC	4067
rs181574993	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55982369	TGATTAACCATTTCA[A/G]AAAGTTTTGAATCTT	4067
rs181579885	snp	A/G	0.00795532	0.062565	intron-variant	LYN	GRCh38.p7	8:55964035	TAACTCTTAAGATCT[A/G]CAGAAAAGGCCATAT	4067
rs181582824	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55920434	CCTTGTTTTGGAGGA[C/T]GGGGGCGGATAATGG	4067
rs181588104	snp	A/C	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:55940072	CTGGACGCGTGGCAG[A/C]GATGCCGGAGAGGGC	4067
rs181600016	snp	C/T			upstream-variant-2KB, missense	LYN	GRCh38.p7	8:55879763	CGGTCACTTCCCCGC[C/T]CTCCGGGCTCAATAT	4067
rs181602188	snp	A/G	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55896340	AAGTTTATAAATAAA[A/G]AAACAGAATAGCAGG	4067
rs181604043	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55915226	GCCTTCCATATTCCA[A/G]CGCATAAGGTTCTTT	4067
rs181624779	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55910418	TATCCTTTTCCCAGT[A/G]TATGTTTTTGTTGAC	4067
rs181666233	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55942963	GATCCTGAAGTTGTC[A/C]TCTGTTATTTTAGTG	4067
rs181670866	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55946675	ATTCACATTGTTGTA[A/C]AACCAATACCGCCCT	4067
rs181687286	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55997502	GTGTCCTCACGTGGT[A/G]GAAGGGGCAAGGCAG	4067
rs181693346	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55977130	GCGGAGATTGCAGTG[A/G]GCCAAGATCGTGCCA	4067
rs181698283	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55960199	AAAGCTGGCAAATAT[A/G]TAAAAGAAATGATAC	4067
rs181721854	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55973757	TTACTAAAAATGGAA[C/G]AATTGTTTGTGAGTT	4067
rs181736169	snp	G/T	0.00636936	0.0560724	intron-variant	LYN	GRCh38.p7	8:55929527	AAGAAAGCATATTTT[G/T]CCCCAATCTGTAACA	4067
rs181765611	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55959682	GATAACATATGTCCA[C/T]GCAAAAACCTGTACA	4067
rs181773920	snp	C/T	0.0170251	0.090679	intron-variant	LYN	GRCh38.p7	8:55942699	CTGAGGCAGGAGAAT[C/T]GCTTGAACCTGGGAA	4067
rs181776023	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55891881	GCAGAGAGAGGACAG[A/G]ATCTTTACTCTTCGT	4067
rs181776832	snp	C/T			intron-variant	LYN	GRCh38.p7	8:56005977	GTAGTCTCAGCAACT[C/T]AGGAGGCTAAGGTGG	4067
rs181782753	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55989666	TAAAACTTTGGTCTC[A/G]TTTAACCAAACCAAA	4067
rs181784915	snp	A/G	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55925629	GGGATGGGCGTTATT[A/G]TTACCTTTTTCATGG	4067
rs181793388	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55925020	CTAATTTTTATATTT[A/T]TAGTAGAGATGGGAT	4067
rs181808538	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55886633	GCAAAACAAAATAGA[A/G]AAAGGAAAATACAAT	4067
rs181816758	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55951104	AAAACTTAGCCAGGC[C/T]TGGCAGCACATGCCT	4067
rs181874854	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55993873	ACTCCATGTAACTCC[C/T]ACAGAAGTCAAGCTT	4067
rs181920005	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55935313	CAGCTTGGCCAGCCC[A/G]GGTTACCAGCTCACC	4067
rs181939084	snp	C/T	0.0103295	0.0711199	intron-variant	LYN	GRCh38.p7	8:55969629	TTTTGTGGGGAGTTC[C/T]CCTGTAATAGTAATG	4067
rs181942539	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55897268	CCATATAAATGAAAA[C/T]TCAGAGTTTAGATTA	4067
rs181942820	snp	G/T	0.00835141	0.0640778	intron-variant	LYN	GRCh38.p7	8:55997375	ATTCCATAGACTGGG[G/T]GGCTTAAACGAGAGA	4067
rs182060487	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55907331	TAACGTATTCTATGA[A/T]AAACATTATTTTCAA	4067
rs182070638	snp	A/T	0.00358779	0.0422022	intron-variant	LYN	GRCh38.p7	8:55934043	CCAGCCTGGCCAATA[A/T]GGTGAAACCCCATCT	4067
rs182074893	snp	A/G	0.00279162	0.0372561	intron-variant	LYN	GRCh38.p7	8:55907678	TCAAGACCAGCCTAG[A/G]CAACATAGGGAGACC	4067
rs182138983	snp	A/T	0.0726307	0.176182	intron-variant	LYN	GRCh38.p7	8:55887616	CACATATATATATAT[A/T]TTTTTTTTCCTGAGA	4067
rs182221911	snp	C/T	0.00597247	0.0543191	upstream-variant-2KB	LYN	GRCh38.p7	8:55877238	GCAAGCTCTACGCTT[C/T]GGGCCATTTATTTTT	4067
rs182227685	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55952480	CAGGAGAATCACTTG[A/G]ACACAGGAGGCGGAG	4067
rs182229617	snp	A/G	0.00874735	0.0655527	intron-variant	LYN	GRCh38.p7	8:55916053	ATGGTATAAAAATTA[A/G]AGCTATCTTAAGTTC	4067
rs182232448	snp	C/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55976526	ACAGCCAGGCACTGT[C/G]TCAGGAGGGATGAGC	4067
rs182254622	snp	C/T	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55917039	AAAATTAGCCAGGCG[C/T]CGTGGTGCATGCCAG	4067
rs182255683	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55883755	GATCATTTTGAGCAC[C/T]TGCTGTGTGCAAGGC	4067
rs182279346	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55953646	GAGTGAAACTTCATC[A/T]CAAAAAAAAGAAAAA	4067
rs182429827	snp	A/G	0.0197687	0.0974348	intron-variant	LYN	GRCh38.p7	8:56004222	CAGGTGTGAGTCACC[A/G]CACCCGGCCTAAATA	4067
rs182454921	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55986448	AAGAGAAAGTAAATG[A/G]GTATTCATTGACAAA	4067
rs182502083	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55895208	GTTAGCAACTGCTGG[A/T]TGCTACAGAGGATTT	4067
rs182507606	snp	C/T	0.0023933	0.0345097	intron-variant	LYN	GRCh38.p7	8:55940575	GAGATGGGGTTTCAC[C/T]ATGTTGGCCAGGATG	4067
rs182514110	snp	A/G	0.00478085	0.0486577	intron-variant	LYN	GRCh38.p7	8:55912476	TATGCCTGTAATCCC[A/G]CACTTTGGGAGGTCG	4067
rs182521152	snp	A/G	0.00438332	0.0466095	intron-variant	LYN	GRCh38.p7	8:55957028	AACAACATCACTGAG[A/G]ATCAGATAAGCAACT	4067
rs182553487	snp	C/T	0.00716266	0.059414	intron-variant	LYN	GRCh38.p7	8:55908343	TCTGCCTCCCAGGTT[C/T]GAGTGATTCTCCTGC	4067
rs182554007	snp	A/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55974432	ATTGGTAAAATGAGG[A/T]AGGTAGGAAAACTCT	4067
rs182556655	snp	C/T	0.00159617	0.0282053	upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55878224	AGTGGAAATTAGCAT[C/T]GTATCGTTTTTTTCC	4067
rs182566371	snp	A/C/G	0.0023933	0.0345097	intron-variant	LYN	GRCh38.p7	8:55932448	TTTTTTTTAGATGGA[A/C/G]CCTCACTCTTTTGCC	4067
rs182682506	snp	A/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:56007694	AGTTTATTGGCCATA[A/T]GCCATTGTGGGAAAT	4067
rs182686561	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55991129	GTCTGAGGTCTATCC[C/T]TGATCCCACTCTGCC	4067
rs182695012	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55970655	GTTAGGAAATTGCTA[C/T]GGCCTTCTTGGGAAT	4067
rs182695666	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55994891	CTGTAACCAACTCTG[G/T]TCTGTTTGAGCCAGG	4067
rs182708271	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55921729	GAGGCCAGCCTGGGA[A/G]AGGCAGGGAGGGGCA	4067
rs182819369	snp	A/C	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:55903762	CTCACACCTGTAATC[A/C]CAGCACTATGGGAGG	4067
rs182819811	snp	C/T	0.00716266	0.059414	intron-variant	LYN	GRCh38.p7	8:55966079	GCAGTGAGCCAAGAT[C/T]GTGCCACTACACTCC	4067
rs182840213	snp	A/C	0.00398564	0.0444627	intron-variant	LYN	GRCh38.p7	8:55926636	TTATTAAGACACAGC[A/C]GGTAACGGCCTGCCC	4067
rs182850733	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55900404	TAGGGATAGGATTTC[A/G]TTGTGTTGCCCAGGC	4067
rs182851762	snp	C/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:56003540	CGGCGTGGTGGCCAA[C/T]GCCTGTAATCCTAGC	4067
rs182853489	snp	C/T	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:55904960	AGCATTTAAACCTCC[C/T]CATGCCCAAGCTGTT	4067
rs182858436	snp	A/G	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55923973	TCTCAAATGGGATGT[A/G]TACACCCTGCCGCAC	4067
rs182865857	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55941681	AAATATTTGTTGAGT[C/G]AATCAATGGACAGGC	4067
rs182882125	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55884161	CTGGAGTGCAGTGGT[A/G]CAATCTCAGCTCACG	4067
rs182974366	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55904844	AAGGTTCCCTACATT[A/G]TTAGACTGCGCATTT	4067
rs182992099	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55974711	TCTCTTTGTCTGGAA[C/T]GTAAGAGATGTGTTA	4067
rs182994646	snp	A/G	0.00279162	0.0372561	intron-variant	LYN	GRCh38.p7	8:55978588	TGGATGAGGTCCCCT[A/G]GAGAGTGTGGGAAGG	4067
rs183002126	snp	A/G	0.00438332	0.0466095	intron-variant	LYN	GRCh38.p7	8:55962875	AGCTTCCATTCAAAA[A/G]GGAAGGCAAAAGGGA	4067
rs183029809	snp	G/T	0.00557542	0.0525036	intron-variant	LYN	GRCh38.p7	8:55998122	GACATGTTCCTTTTT[G/T]TTTTTTTAAGATGAC	4067
rs183064618	snp	C/T	0.00517822	0.0506191	intron-variant	LYN	GRCh38.p7	8:55921338	TTGTCTGCAAAGAAG[C/T]GGGATAGACAGGGTC	4067
rs183064917	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55888399	ACTTCATGGCATTAA[C/T]GAAGGGGAATCACTG	4067
rs183067698	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55908528	GGGATTCCAGGCCTG[A/T]GCCACCGTGCCAAGG	4067
rs183077894	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55877854	ATAAATCAGTCATCA[A/G]TCAATTAACCAATCA	4067
rs183078699	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55927065	ACATTAGTGTGGTAC[A/G]TTTGTTATCACTGAT	4067
rs183095235	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55916499	ATGGTTCACAAAAGC[A/G]GTGAAGACATGTATC	4067
rs183105711	snp	C/G	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55978326	AGGATGGGCCTGAGC[C/G]AGGTCAGTGTTGCCT	4067
rs183114751	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55883003	GCATTTAATACACTT[A/T]ACCTACTAAACATTA	4067
rs183118337	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55961451	TTAACAGAGGGATGA[A/G]AACCACCCTATTGTT	4067
rs183130066	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55943612	CATTTTTATAGTTTC[C/T]CTAGTCTGACATGTT	4067
rs183131776	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55948400	GGGTTCATGGGCCCA[G/T]CCTAGCTTGAGTTCT	4067
rs183148406	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55935539	AGCACTTTGGGAGGC[C/T]GAGGCGGGTGTATCA	4067
rs183168308	snp	A/G	0.00358779	0.0422022	intron-variant	LYN	GRCh38.p7	8:55985412	TGGTATTTTGAAAAC[A/G]CACTTCAAAGGGGTT	4067
rs183241306	snp	A/G/T	0.00677088	0.0578511	intron-variant	LYN	GRCh38.p7	8:55974919	ATTGACATGGTTTGC[A/G/T]GTTTAACCAGGAGGC	4067
rs183247942	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55957996	GCCTGGATGCCTGGC[A/G]TCAAAAGTGCTGCTG	4067
rs183249126	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56003307	ACCTTGGGATCCTCC[C/T]GCCTTGGCCTGCCAA	4067
rs183262885	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55984510	AGTCATTCTTGACCC[A/T]CTTCCTTTTACATTG	4067
rs183424892	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55948015	ATCTCTCTCTGTCAT[C/T]CAGGCTAGAATGCAG	4067
rs183425202	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55912242	CTTTTGCAATGTATC[A/G]TTAAGGATGCATTGC	4067
rs183551459	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55952831	CTTGGTAAAGTCAAA[C/T]GGATATAACACTACC	4067
rs183577914	snp	A/G/T	0.00398564	0.0444627	intron-variant	LYN	GRCh38.p7	8:55990154	TGAGGCAGGAGAATC[A/G/T]CTTGAACCCAGGAGG	4067
rs183585795	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55927325	TTCCAGAGTGTCATA[C/T]GGTTGGAATCACACA	4067
rs183611187	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55930973	AAGTTCTTACTCCCA[C/T]GGACAATTAGAGTTT	4067
rs183656773	snp	C/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55965604	TCGTAATCACACCAT[C/T]GGAAATAACCAGCAT	4067
rs183659130	snp	C/T	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55894593	GCTGGAGTTCATTGG[C/T]GCTATCTTGGCTCAC	4067
rs183738397	snp	G/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55971122	TCCTCATCTGAGTTG[G/T]AAATTCAAGTGTGCC	4067
rs183744123	snp	A/G	0.00636936	0.0560724	intron-variant	LYN	GRCh38.p7	8:55890931	ATAAGGTTTTGCCAT[A/G]TTGTCCAGGCTAATC	4067
rs183744314	snp	A/C	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55937109	ATCCAACTCCATAGT[A/C]CTTACTTCAGAATAT	4067
rs183769735	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55970366	TTTCCTGAAGTGTAT[G/T]TAAGAGCAGAAGCAA	4067
rs183792107	snp	C/T	0.00478085	0.0486577	intron-variant	LYN	GRCh38.p7	8:56008042	GAGAATCGCTTGAAC[C/T]TGGGAGGCGGAGGTT	4067
rs183801819	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56006877	TCTTCTTATTTCTTT[A/C]TTTCACAAGACTTGT	4067
rs183803415	snp	A/G	0.00358779	0.0422022	intron-variant	LYN	GRCh38.p7	8:55909794	CCACTTTTGAATAAT[A/G]GCCATTCTGAGTGGT	4067
rs183806411	snp	C/T	0.00716266	0.059414	intron-variant	LYN	GRCh38.p7	8:55944775	CGTGAGCCACCACAC[C/T]CAGCCTGTTTTTTGT	4067
rs183851347	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55896646	GTATCTTAGAAATTA[A/G]AGTATAATAAAAAAA	4067
rs183856481	snp	C/T	0.0103295	0.0711199	intron-variant	LYN	GRCh38.p7	8:55915533	AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT	4067
rs183862825	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55934784	ACTTCCCACCTCACC[C/T]CCCTTTCCCAATTGA	4067
rs183873878	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55975210	ACCTCAGCTTTCTCA[C/G]TATACAAATGTTAAC	4067
rs183878330	snp	A/G	0.0023933	0.0345097	intron-variant	LYN	GRCh38.p7	8:55958696	TTAGGTACCTCAAAT[A/G]ATTAGAATCATACAG	4067
rs183885700	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55913267	GCTATGTTGCTTTCT[C/T]TCCAAAGGTATTCAG	4067
rs183892491	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55885592	GTATTCATTCTGCCT[C/T]CCACTGAAGCAATGA	4067
rs183892609	snp	A/G	0.00398564	0.0444627	intron-variant	LYN	GRCh38.p7	8:55932899	CTCTCACTTATGAAT[A/G]GGAGCTAGGCATTGA	4067
rs183897534	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55906781	ATGAAATGTATCCCA[A/G]TTGAACAACAGTTGA	4067
rs183908158	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55996479	CTGTGTGAAAAATTC[A/G]AATCAGAGTTTTCTC	4067
rs183909340	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55951551	ATGATCGTAGTCTCA[C/G]CTACTTGAGAGGTTG	4067
rs183915683	snp	G/T	0.00318978	0.0398085	intron-variant	LYN	GRCh38.p7	8:55949736	CTGGCTTCTTTTCTT[G/T]GTCTCTCTCTCTCTC	4067
rs183936519	snp	C/G	0.00398564	0.0444627	intron-variant	LYN	GRCh38.p7	8:55917284	TTGAACTCCTAGGCT[C/G]ATGTGATCGTCCCGC	4067
rs183938328	snp	A/C	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55991570	ACTTTTCATTGTGTA[A/C]AAGATGCCAAGAGTT	4067
rs183951979	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55954460	AACATTAAGTATTGC[C/T]TTCTCAGGCTGGCAA	4067
rs183953840	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55967003	TTATCAAACAGTATA[C/T]CCACTACCGAAAAAT	4067
rs183988183	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55939226	TCTGAATGGGGGACC[C/G]CAAACACTTTGTGAG	4067
rs184016257	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55972270	CTAAGCACTGGCTCC[A/G]TTTGAGTTCATCTTT	4067
rs184023715	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55956148	CTTTTTTCCTCCTTT[A/G]ATGTTTATATTTATT	4067
rs184054240	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56009461	GACGTTTATTTTTCC[A/G]GGGTTCTGGAGTTTC	4067
rs184054358	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55992589	ACTTCCTCCCCAACC[A/G]TTATGATGGTAACAG	4067
rs184096736	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55995266	GTTATCACCACTGCC[A/C]ACCTTCTGTTGACTT	4067
rs184422597	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55902389	TTGGAGTGCAGTGGC[A/G]TGAATTCAGCTCACT	4067
rs184438756	snp	A/G	0.00438332	0.0466095	intron-variant	LYN	GRCh38.p7	8:55918990	AATTGCATGAGCTCA[A/G]TTGTTCGAGACCATG	4067
rs184443966	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55938596	CAATGTTACCACATT[C/T]GCATTTTTCTCATTG	4067
rs184465724	snp	G/T	0.00119737	0.0244387	upstream-variant-2KB, synonymous-codon	LYN	GRCh38.p7	8:55879689	TCGCCAGGTTTCTGT[G/T]CCTTCAAAGCCCTGC	4067
rs184484018	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55955312	AGTCTTTCTGCACAT[A/G]TTTGCAGAATTCAGG	4067
rs184490960	snp	A/C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55895959	ACTCATGCATCATCA[A/C/T]CAGTCCTGTGGGGAA	4067
rs184506833	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55959321	CAAGTCCCTTTCTCA[C/T]TTTTTAAATTGTGTT	4067
rs184527127	snp	A/G	0.00755907	0.0610114	intron-variant	LYN	GRCh38.p7	8:55924936	AGCCTCCGCCTCCCA[A/G]GTTCAAGCGATTTTC	4067
rs184541301	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55996965	ATCTCTACTAAAAAT[A/G]CAAAAACTAGCATGG	4067
rs184633186	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55906302	GGGAGGCTGAGGTGG[A/G]AGGATTGCTTGAGGC	4067
rs184661273	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55968532	AAAGTGCTGGAATTA[C/T]AGGTGTGAGCCACCA	4067
rs184666902	snp	C/T	0.00279162	0.0372561	intron-variant	LYN	GRCh38.p7	8:55942582	ACTAGGTCAGGAGCT[C/T]GAGACCAGCCTGGCC	4067
rs184679700	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55976465	CTGAGCCCCCTCACC[C/T]TCTTGGTGTGGCCCG	4067
rs184694414	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56005228	ATAAGGGGAGTCATA[C/T]AGTTTTGCCCTAATG	4067
rs184706855	snp	C/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:56001681	TCTGATGTTATATAT[C/T]TCTATCTCCATCTAT	4067
rs184767771	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55884518	CTGGAGTGCTTTGGC[A/G]TGATCCCAGTTCACT	4067
rs184768672	snp	A/G	0.0023933	0.0345097	intron-variant	LYN	GRCh38.p7	8:55928876	TCTAGCTTTTCTCCT[A/G]TGTTATCTCCTAGGA	4067
rs184784032	snp	A/G	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:55945750	CCCACTGAAATAACA[A/G]GGGATGCCATCTGTC	4067
rs184785959	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55963513	TCAGTGATGCTCAGC[A/G]AAGAACACAGAATGA	4067
rs184786545	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55924773	CTCCAGTTCACTTCT[A/G]GTATCATATACTGCA	4067
rs184792198	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55946505	AAAGGTATGTTTTCA[C/T]AGCAACATAGTTAAA	4067
rs184796975	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55989035	AACACTTCATTATTT[A/G]TCCAAAGCATTGCTC	4067
rs184802868	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55891224	GAACATGGTGGTGCA[C/T]GCCTGTAATCCTGGC	4067
rs184808990	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55910265	GATTTTCTTCTAGTA[C/T]TTTTATGCTTTCATG	4067
rs184814235	snp	C/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55919637	AAGAAAAACCCATGC[C/G]CGTGGGAACAAGTAA	4067
rs184819112	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55980604	GTATACAGTCAAATT[C/T]GGATTTTGGATAAAC	4067
rs184825691	snp	C/T	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:56000510	GAGGTGGGTGAATCA[C/T]GAGGTCAGGAGTTCG	4067
rs184829723	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55981845	CCTGTGGGAAAAACA[A/C]AGTGCAGCTTTGTTT	4067
rs184887669	snp	A/G	0.00398564	0.0444627	intron-variant	LYN	GRCh38.p7	8:55963226	TGAGCTCTAGGGTGA[A/G]TGGGAGTGGATTTGC	4067
rs184894070	snp	C/T			intron-variant	LYN	GRCh38.p7	8:56005769	TATGATTATATTTCT[C/T]TATCAATTTTATACA	4067
rs184903265	snp	C/T	0.00279162	0.0372561	intron-variant	LYN	GRCh38.p7	8:55989427	TGTGGTCATAGGCAA[C/T]CCACTTCTCAGTGGG	4067
rs184926837	snp	C/G	0.00755907	0.0610114	intron-variant	LYN	GRCh38.p7	8:55999772	AGGTCGGGAGTTGGA[C/G]ACCAGACTGACCAAC	4067
rs184939993	snp	C/T	0.00597247	0.0543191	intron-variant	LYN	GRCh38.p7	8:55959801	GGTGTATTCATACAA[C/T]GGAGTATTTGGCAAT	4067
rs184943902	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:56004769	TTAGATAAGGATATG[A/G]CCACATACTTTTATT	4067
rs184969460	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55997385	CTGGGTGGCTTAAAC[A/G]AGAGACATTTATTTC	4067
rs184983138	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55976629	AAGGGCTGTCAGAGT[A/G]GGCACCGCATGCTAC	4067
rs185220953	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55908392	TGGGATTACAGGCAC[C/T]CCCCACCGCGACCTG	4067
rs185234033	snp	C/G	0.00398564	0.0444627	intron-variant	LYN	GRCh38.p7	8:55926637	TATTAAGACACAGCA[C/G]GTAACGGCCTGCCCT	4067
rs185251029	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55969556	ATTAGAGGGGACTGC[A/G]TTTGACCAATGCCAG	4067
rs185253880	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55896183	GCTGAAGTGAGTGGG[C/T]CCCTTGAGTCCAGGA	4067
rs185261104	snp	C/T	1.6649e-05	0.00288518	synonymous-codon	LYN	GRCh38.p7	8:55952111	CATGATTAAACATTA[C/T]CAAAGTAAGTAAAAA	4067
rs185262875	snp	C/T	0.00358779	0.0422022	intron-variant	LYN	GRCh38.p7	8:55887702	GCAACCTCCACCTCC[C/T]GGGTTCAAGTGATTC	4067
rs185266412	snp	A/G	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55935100	GCTCTGTGATCTGAG[A/G]GATTCCCGGCACCGA	4067
rs185322191	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55991996	TTTACGTGATTAGTC[C/T]CATTTTTGGTAATAG	4067
rs185354942	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55929581	TACCAGCAATTAAAA[C/T]ATCAGATTTCCTGGC	4067
rs185361372	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55964635	ACTTTGGAAGACCAA[C/G]GTGAGCAGATCAGCT	4067
rs185387076	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55901668	GATTCAGAAAGAGCA[C/T]TGGGCATACACTTCA	4067
rs185442478	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55947058	TTCGAGACCAGCCTG[A/G]TCAACATGGTGAAAC	4067
rs185449503	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55971567	TGAGTGGTCACAGCC[A/G]TTCCATCTGCTGGGG	4067
rs185468057	snp	A/G	0.00279162	0.0372561	intron-variant	LYN	GRCh38.p7	8:55910520	TGTATCTATTTTTAT[A/G]CCAGTACCATGCTGT	4067
rs185470300	snp	A/C	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55982535	ACCTTCTACCTCCCC[A/C]ACCCAGGACCCCCAG	4067
rs185475755	snp	A/G	0.00279162	0.0372561	intron-variant	LYN	GRCh38.p7	8:56008212	GTTGATCCCAAATGC[A/G]GATAGTGCCCCGCAA	4067
rs185477477	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55911287	TATATATATATATAT[A/T]TTTTTTTTTTTTTTA	4067
rs185486837	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55930278	TCCACTTCTTTTAGG[C/T]GTCTTGAGCTGAGTT	4067
rs185493854	snp	A/T			utr-variant-3-prime	LYN	GRCh38.p7	8:56010543	TATATACATAGCATG[A/T]CATTTCTTTGTGCTT	4067
rs185501362	snp	C/T	0.00159617	0.0282053	upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55878661	GGTTTCAATCACACA[C/T]CTTCCCATGGGTATT	4067
rs185517388	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55893052	CAAAGCCATTTGGTT[C/T]GGCAAATAAACAGAT	4067
rs185556750	snp	A/G	0.00279162	0.0372561	intron-variant	LYN	GRCh38.p7	8:55950985	TGGTGGCTCACACCT[A/G]TAATCCTAACACTTT	4067
rs185583934	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55914712	CACCTTACCCTTCCA[C/G]ACATGAGAAAACAGT	4067
rs185589916	snp	A/C	0.0271762	0.113356	intron-variant	LYN	GRCh38.p7	8:55987744	TTTAAAGGAAGGAGC[A/C]AATGTGGATGAATGC	4067
rs185615684	snp	A/G	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:55935572	TGAGATCAGGAGTTG[A/G]AGACCAGCCTGGCCA	4067
rs185634012	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55997804	AAATGTTAAGACATG[G/T]CCAGGCGCGGTGGCT	4067
rs185638031	snp	C/T	0.00438332	0.0466095	intron-variant	LYN	GRCh38.p7	8:55952992	GGCTCCTTTCTATGA[C/T]CTGCTCGAAGGGGAT	4067
rs185644618	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55977236	TTCATTCTCAGTTGT[A/G]GAAGACTAAACTGTT	4067
rs185676302	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55970550	GAAGCCCAGTGTATG[C/T]AGCAAAAGAGATTTA	4067
rs185726972	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55933646	TTTGTCGATAATTAC[A/G]GGACTGTCAAGGCTG	4067
rs185729119	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55967407	GCAACCCCTGCCTCC[C/T]GGGTTCAAGCGATTC	4067
rs185757878	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55997859	GGAGGCCAAGGCGGG[C/T]GGATCACGAGGTCAG	4067
rs185773069	snp	A/G	0.0023933	0.0345097	intron-variant	LYN	GRCh38.p7	8:55960828	GAACAAATACTAGGA[A/G]GTGACCTGTTCTTTG	4067
rs185783871	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55994484	GATTTATGCAAATGC[A/G]GGATGTGGGTAGGTG	4067
rs185790277	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55974605	ACCAGTATGTTGGTC[A/G]TAAATCAGGCTTGAA	4067
rs185815698	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	LYN	GRCh38.p7	8:56012207	CACACACAGTCTCCT[C/T]ACTTAGCTATAGGTT	4067
rs185891847	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55977837	GACGAGAGGATTGAT[C/T]GAACCCGGGAAGTTG	4067
rs185913303	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55994058	CAGCCAAAGGAGTCT[C/T]TGATTTCTTCCTGCT	4067
rs185916568	snp	A/C	0.00398564	0.0444627	intron-variant	LYN	GRCh38.p7	8:55973894	AGGACCAGCCTGGAC[A/C]ATGTGGCAAGAATCT	4067
rs186138107	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55897039	GCCACTGCACCCGGC[C/T]TAAACTTCATTTAAA	4067
rs186188735	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55984284	GCTGTCTAGACTCCG[A/G]CCACTCCGAAGCTTC	4067
rs186196666	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55965282	CAAGTGTTCTGAGGT[C/G]AAGAAATTGTGGGAA	4067
rs186199008	snp	A/G	0.00438332	0.0466095	intron-variant	LYN	GRCh38.p7	8:55911600	GTCTGAATTGGGGAA[A/G]TATTTATACATATGT	4067
rs186202949	snp	G/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55947841	CCCTTTCTTGTAATG[G/T]GTATGAGGCCTCCTT	4067
rs186204998	snp	A/G	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:55930552	ATTTCCCTACCTTAC[A/G]TAAGTTTCCATGAGC	4067
rs186205603	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	LYN	GRCh38.p7	8:55876821	ATCCTGGCCTCAAGC[A/G]CCATGACCACGCATG	4067
rs186221464	snp	C/T	0.00279162	0.0372561	intron-variant	LYN	GRCh38.p7	8:56003106	GCTCTGTTGCCCAGG[C/T]TGGAGTGCAGTGGCG	4067
rs186241699	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55920568	AGATGAGGAAAATGA[A/G]GTTTAATGAAGTAAC	4067
rs186251882	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55940524	GGGACTACAGGCGTG[C/T]GCCACCACGCCCAGC	4067
rs186261625	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55943375	AAGGTCAGGAGTTTG[A/G]GACCAGCCTGGCCAA	4067
rs186269926	snp	A/G	0.0023933	0.0345097	intron-variant	LYN	GRCh38.p7	8:55882496	TTTATAAATAAGGAC[A/G]CCATGTATACATGCC	4067
rs186276400	snp	A/G/T	0.00438556	0.0466571	intron-variant	LYN	GRCh38.p7	8:55915842	AGCGAGCGAGCGAGA[A/G/T]ACATCGAGGATAAGA	4067
rs186278969	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55907698	ATAGGGAGACCCTGT[C/T]TCTACAAAAATAAAA	4067
rs186307760	snp	G/T	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:56007347	CTGAGGCCATATCAT[G/T]TTGTGGAGACTAAAA	4067
rs186315992	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55881893	CATAGTAGGTGCTCA[G/T]TTCGAGATTACTTGG	4067
rs186365094	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55883577	AATGGTTAATACAGA[A/G]GTACCTGAGTAATAC	4067
rs186368208	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55887452	TGAGTGCTGTTTTTA[C/T]TTCTGTACGTCTTTA	4067
rs186395338	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55957037	ACTGAGAATCAGATA[A/G]GCAACTTACTCAAGG	4067
rs186403590	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55982997	GACACTCATTGCCCC[G/T]CCCCCATGTCACACG	4067
rs186442277	snp	A/G	0.0115144	0.0749975	upstream-variant-2KB	LYN	GRCh38.p7	8:55877283	TAATTTTTTTATTGT[A/G]GGGGGGGTCTCACGA	4067
rs186443648	snp	C/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55925077	ATCCGCTTGCTTCAG[C/G]CTTCCAAAGTGTTGG	4067
rs186444541	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55947291	GATGTTTATCCATTC[C/T]TCCATCAATAGATGT	4067
rs186445493	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55926003	AAACTTTTTATCTTG[C/T]TTTATAAAAATTAAA	4067
rs186456514	snp	A/G	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55921392	ATCGAGGAGAGAGCT[A/G]TACACGTACTAACTG	4067
rs186460106	snp	A/G	0.00557542	0.0525036	intron-variant	LYN	GRCh38.p7	8:55960359	CTTATATTGAATGGA[A/G]GAAGGAAGGAAAAGA	4067
rs186461671	snp	A/T	0.00279162	0.0372561	intron-variant	LYN	GRCh38.p7	8:55886357	CGATTCTGCTGCCTC[A/T]GCCTCCCGAGTAGCT	4067
rs186502608	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55990343	AAGGTATAGGAAGTG[A/G]TGGTTGTAGAAGCAA	4067
rs186578958	snp	C/T	0.00279162	0.0372561	intron-variant	LYN	GRCh38.p7	8:55904329	TGAAAATAAATTTCT[C/T]AGAATATGATATGAA	4067
rs186599815	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55954095	TAAATTATGTCAGAA[A/G]CATCATTTATTTTGT	4067
rs186600185	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55928807	ATTTTTTCTTTCATG[A/T]TCATGGATCATTTTG	4067
rs186620596	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55964921	GACCGTCCACTCCAC[A/G]TCACCTTTCCTTAGG	4067
rs186629445	snp	A/C	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:56007900	GAGACAGGCAGACGA[A/C]TTCAGGTCAGGAGTT	4067
rs186629631	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55991255	CTTCCTGTTTCACAC[C/T]AGCAGTGGGGGAGAA	4067
rs186634091	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55946068	ACAACCGATCTGCGG[A/G]CCAAAACTCCCTCTG	4067
rs186638987	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55910106	CAGGTTGTCGGTTCA[C/T]TCCTGTTGAGTATTT	4067
rs186640347	snp	A/G	0.0023933	0.0345097	intron-variant	LYN	GRCh38.p7	8:55970815	TGGCTCTGCCACTCG[A/G]TAGCTATACCGCTTC	4067
rs186655508	snp	C/T	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:55940925	ATGGCTTGCGGAGAC[C/T]GTCATTTTGCTTTTA	4067
rs186657234	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56002262	ATCTCTACTAAAAAT[A/G]AAAACAATTAGCCAG	4067
rs186681547	snp	C/T	0.00398564	0.0444627	intron-variant	LYN	GRCh38.p7	8:56008223	ATGCGGATAGTGCCC[C/T]GCAATTTGAAAAACA	4067
rs186769212	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	LYN	GRCh38.p7	8:56011194	AGGATATGAAGGAAC[A/G]TAAGTGACTACAAGG	4067
rs186818829	snp	A/G	0.00358779	0.0422022	intron-variant	LYN	GRCh38.p7	8:55984550	TTCCTCAGCAAGTCT[A/G]GGGTTCTACCCTCAA	4067
rs186901235	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55892491	TTTGATGATACAGTT[A/G]TATTAATATTTCTAG	4067
rs187009257	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55998975	TTTCCCACATTCTGT[A/G]TTATATATATGAACC	4067
rs187055728	snp	A/G	0.0023933	0.0345097	intron-variant	LYN	GRCh38.p7	8:55903054	GGGTTTCACCATATC[A/G]GCCAGGCTGGTCTCG	4067
rs187073867	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55916520	GACATGTATCTACAC[C/T]GAGGACAGCATGTGA	4067
rs187098009	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55973029	GATTGGTCATTGGGA[A/G]TAGAAATAACCCAGT	4067
rs187104069	snp	C/G	0.000798403	0.0199641	upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55877921	AATTTCTGGGAGGTA[C/G]AGTGGGGAATAGATA	4067
rs187105731	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55899181	AGAAAATATAGTAAG[A/G]ATAGCAATCCTTTAT	4067
rs187126859	snp	A/G	0.0023933	0.0345097	intron-variant	LYN	GRCh38.p7	8:55939352	CCATGACAATGGTGG[A/G]AAGAAATTAAGCATA	4067
rs187149624	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55996679	TTTCCTTTCTTCCTT[C/T]CTTCTCCTTAACTTT	4067
rs187192360	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55942141	CTTTGTAACTTTATC[A/C]TTTGAAGAATGTATA	4067
rs187198633	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55916129	ATGGTAAATTATCTC[A/G]TGATAGTTTCATGTT	4067
rs187228199	snp	A/G	0.00438332	0.0466095	intron-variant	LYN	GRCh38.p7	8:55932627	GGTTTCGCCATGTTG[A/G]CCAGGCTGGTCTCGA	4067
rs187228849	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55905130	AAACATGGTGACCTG[G/T]CTGGGTGTGGTGGCT	4067
rs187229810	snp	A/G/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55974942	CAGGAGGCCAGATCC[A/G/T]CTCCCCACTCCATAT	4067
rs187238744	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55958207	GGGATTGGGAAAACC[A/G]CCTTGCTTCTAATTC	4067
rs187240090	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55924424	CTGGAGTGCAATGGT[A/G]TAATCTTGACTCACT	4067
rs187244564	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55966168	TGGTAGAGTGCCAAT[A/C]AAAACGTTTTTTTGC	4067
rs187249750	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55948565	TAGGCATGCAGGACA[A/G]TGCTCAGAATAAGAA	4067
rs187252163	snp	A/G	0.00438332	0.0466095	intron-variant	LYN	GRCh38.p7	8:55920267	GACGCATCAGACATT[A/G]TCTGGAGTGCTGTGA	4067
rs187254581	snp	C/G	0.0023933	0.0345097	intron-variant	LYN	GRCh38.p7	8:55895656	AGGAATTGGCTTCTA[C/G]TCAATGCTTTGTCAA	4067
rs187261937	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55995706	CAGGGAGGGAATGAG[C/T]GTTCCACACAGAGGC	4067
rs187268792	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55952535	ACTGCACTCCAGCCT[A/G]GGTGACAGAGCAAGA	4067
rs187279673	snp	G/T	0.00597247	0.0543191	intron-variant	LYN	GRCh38.p7	8:55956483	TCACTTTTATTTAAA[G/T]TGATCCAAAAGTTTA	4067
rs187290593	snp	G/T	0.0252325	0.109451	intron-variant	LYN	GRCh38.p7	8:55894547	GCTAATTTTTTTTTT[G/T]TTTTTGACGGAGTCT	4067
rs187312129	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55989981	CAGTGACTCATGCCT[A/G]TAATCCCAGTACTTT	4067
rs187330285	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55993644	CTACCTGGTCAATTT[G/T]CTATTAAGATGAAAC	4067
rs187392142	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55897591	CAAAATCTTTAGTAA[G/T]GGGATATAAGCACTC	4067
rs187453900	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55963379	CTAGCAGAGCTGTAC[G/T]TAGAGAGATGTGGGC	4067
rs187457370	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55970145	AGCTTTTAAATGATG[C/T]GTATGTTTTATTTAA	4067
rs187461138	snp	A/C	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55936345	TTGCATCAGTAAAGA[A/C]GTGCAGCTTTTAGGC	4067
rs187483147	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55999971	GTGAGACTCCATCTC[A/G]AAACAAAAAAAAGAC	4067
rs187504843	snp	A/G	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55935406	AATAATGACCATGGT[A/G]TGTAAGGCAAAAAAT	4067
rs187506328	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:56006300	CTTGGTCACAAGCAA[A/G]GCTCAGAAAATAATA	4067
rs187519045	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55884167	TGCAGTGGTGCAATC[C/T]CAGCTCACGGCAATC	4067
rs187658138	snp	A/C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55904853	TACATTATTAGACTG[A/C/T]GCATTTTACCCTTTT	4067
rs187702937	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55917044	TAGCCAGGCGCCGTG[A/G]TGCATGCCAGTAATC	4067
rs187711825	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55883833	AGGCTGATAATGAAG[A/C]GAAGAACATGGAAGA	4067
rs187745678	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55981197	CACCTCTTATCAACA[A/G]GCACCTTCCCTGACC	4067
rs187757737	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55901427	ACTGTTTAATTGAAC[A/G]GTTTCATCTCAAGGC	4067
rs187810348	snp	C/T	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:55901673	AGAAAGAGCATTGGG[C/T]ATACACTTCAGGAAA	4067
rs187834575	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55978402	GAGGACCGCCATTGC[A/G]GGCACGGGGTTGAGG	4067
rs187840793	snp	A/C	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55908955	ATACATAATTTTATT[A/C]TTTTTTGTGGCTGAA	4067
rs187842593	snp	C/T	0.00318978	0.0398085	upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55878956	CTCTGTAAATGTTTG[C/T]TATTAATGCAATGCT	4067
rs187844634	snp	C/G	0	0	intron-variant	LYN	GRCh38.p7	8:55961676	TCTATTTATAAGTCT[C/G]CATGAGCTTCATTGT	4067
rs187848946	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55927169	GATTTTGACAAGTGT[A/G]TAATGACATGTATTC	4067
rs187850409	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55950147	CACTGGATGGATATT[C/G]CAGATTTTGTCCATT	4067
rs187872712	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56004584	CAGGCATGAGCCACC[A/G]TGTGCAGCCACAAAA	4067
rs187878996	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55987635	TGGGCAGGCTGGTCT[C/T]GAACTCCTAGCCTCA	4067
rs187879848	snp	G/T	0.0162398	0.0886349	intron-variant	LYN	GRCh38.p7	8:55997941	TACAAAAAATTAGCC[G/T]GGCATGGTGGTGGGT	4067
rs187890370	snp	G/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55967197	CAAATGAATTACTAT[G/T]TATTTCAAAAAGGAA	4067
rs187893995	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55910046	AAATTCTGCATATTA[A/G]TCCTCTGTCGAAGGC	4067
rs187947741	snp	C/G	0.00438332	0.0466095	intron-variant	LYN	GRCh38.p7	8:55945070	CAGATATGACAAAAT[C/G]CACGCTATGGATTGA	4067
rs187976737	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55979424	GAACTTAAATTATTG[A/G]TTTTTAAAAATATAT	4067
rs188007397	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55972467	GGAGTAGGGCCTGTA[C/T]GCTTCAGCTTCAGCC	4067
rs188023974	snp	G/T	0.00398564	0.0444627	upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55878258	TAAGAATGAAGAGAT[G/T]AACTTAGTGAGGACA	4067
rs188035479	snp	C/T	1.64792e-05	0.00287042	synonymous-codon	LYN	GRCh38.p7	8:56010048	CCAACGTTTGACTAC[C/T]TACAGAGCGTCCTGG	4067
rs188053180	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55992750	GTCCAAGATCAAGGC[A/G]CCAGTAGATACAGTG	4067
rs188094520	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55985675	TCTCAGCTATCTGAC[A/G]TGGTGTATATTCATG	4067
rs188123367	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55890981	CAATCTACCTGCTGT[A/G]GCCTCCCAAAGTGCT	4067
rs188163347	snp	G/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55969618	AAAGCCAATCATTTT[G/T]TGGGGAGTTCCCCTG	4067
rs188175679	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55890520	TGATGGAAAATCATA[C/T]GGTAGTTCCTCAAAA	4067
rs188179700	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55965834	TATTAGAGAAAAATA[C/T]TAGTCCTCGGCTGGG	4067
rs188188148	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55927703	AGCTGTGTGTGGTGG[C/T]GGGTGCCTGTAATGC	4067
rs188196639	snp	A/G			intron-variant	LYN	GRCh38.p7	8:56005812	GGTCTGACTGGGCAT[A/G]GTAGCTCATGCCTGT	4067
rs188200807	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55989463	TTGATGACACAAAAC[C/T]GCAGTGCCTCATGAG	4067
rs188202593	snp	C/T	0.0119091	0.0762411	intron-variant	LYN	GRCh38.p7	8:55931195	ATATAATATGTAACT[C/T]GTACATAGCACATAT	4067
rs188220744	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55963210	CTGATGCAAGCATGC[A/G]TGAGCTCTAGGGTGA	4067
rs188301513	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55887614	CACACATATATATAT[A/T]TTTTTTTTTTCCTGA	4067
rs188363777	snp	A/G	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55976054	AAGTCACAAAATGCT[A/G]TTCTCTTTGGGTACT	4067
rs188373579	snp	C/T	0.0146672	0.084371	intron-variant	LYN	GRCh38.p7	8:56004015	TCACCTCACTGCAAC[C/T]TCCTCCTTCTGAGTT	4067
rs188467491	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB, missense	LYN	GRCh38.p7	8:55879690	CGCCAGGTTTCTGTG[C/T]CTTCAAAGCCCTGCG	4067
rs188477388	snp	A/C	0.00636936	0.0560724	intron-variant	LYN	GRCh38.p7	8:55948265	AGGTGTGAGCCACCA[A/C]ACCCAGCCTGGTTTC	4067
rs188524868	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55991997	TTACGTGATTAGTCT[A/C]ATTTTTGGTAATAGG	4067
rs188527191	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55972069	TTACCAAATCCAGCC[C/T]GTGCCAGGTGAACTC	4067
rs188534955	snp	C/G	0.00438332	0.0466095	intron-variant	LYN	GRCh38.p7	8:55919224	AGGAAAAGTGAACAT[C/G]TGTGAGAATCTAAAC	4067
rs188538014	snp	C/T	0.00874735	0.0655527	intron-variant	LYN	GRCh38.p7	8:55894983	CCACAGTGCCAAGCC[C/T]AAAATTTTTTGTATA	4067
rs188539353	snp	A/C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55955368	TTCTCCGTGTGGATC[A/C/G]GCATGTGTCAGAACT	4067
rs188543500	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55938944	TGTAAAGTCATCTGG[C/T]CGTATGGTTTCTTCA	4067
rs188668992	snp	A/T	0.00716266	0.059414	intron-variant	LYN	GRCh38.p7	8:55896666	TAATAAAAAAATTTT[A/T]AAAAAAAGAAACATA	4067
rs188673214	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55989073	CTGGTGGTAGCAGCC[A/G]GGTATGTGTGCTGAG	4067
rs188677907	snp	A/G	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:55969050	CTTTTGGAGGCCAAG[A/G]TGGGAGGATTGCTTG	4067
rs188680076	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55915702	GAAGAGCAAGACTCC[A/G]TCTCAAAAAATAATA	4067
rs188687938	snp	A/T	0.00874735	0.0655527	intron-variant	LYN	GRCh38.p7	8:55951728	GCTAAATAATAATTT[A/T]AAAAAAATTATCATG	4067
rs188689732	snp	C/G	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55934787	TCCCACCTCACCCCC[C/G]TTTCCCAATTGACCC	4067
rs188697458	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55941441	TCTTCCTGGAATCTC[C/T]TTGCTGACTTTGCAA	4067
rs188736332	snp	A/G	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55974784	ACTGCTTTATCTTCA[A/G]AGCCTTGATTAGTAA	4067
rs188751400	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55913808	AACATGAAGGAGGCT[C/G]CTTATGGGATGGGTT	4067
rs188823270	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55912401	CTATACCATGCCTGC[A/G]CTTAAGTAGTTTTTG	4067
rs188837925	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55917802	ATTAAGGAATATGCT[G/T]GAGATATTCAATGGC	4067
rs188857989	snp	G/T	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:55889176	CCCGCCACCAGGCCT[G/T]CGTAATTTTTTTGTT	4067
rs188877507	snp	C/T	0	0	intron-variant	LYN	GRCh38.p7	8:55991605	CAGAACCCCCCACCC[C/T]CAGGATTTGCTCTCT	4067
rs188897440	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55907578	TTTTTGGTGGAAAAT[C/T]AAACTTAGTTGGGCA	4067
rs188898282	snp	G/T	0.00597247	0.0543191	intron-variant	LYN	GRCh38.p7	8:55954525	AGGGGATTCTTTTCA[G/T]CTACCTACTTTAAAA	4067
rs188924505	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55959969	CCAGAATAGGCAAAT[C/T]TAGAGTTAGAAAGTA	4067
rs188932822	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55942947	AATTCAAAATAGTAC[A/G]GATCCTGAAGTTGTC	4067
rs188956499	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55925404	CTGGGATTACAGGTC[C/T]GAGCCACTGCGCTCC	4067
rs188960710	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55997449	TTTCATGTCTGATGA[A/G]GGGCCATTTCCTGGT	4067
rs188964938	snp	A/G	0.00358779	0.0422022	intron-variant	LYN	GRCh38.p7	8:55977046	AAAAGTTAGCCGGGC[A/G]TGGTGGTGTGCGCCT	4067
rs188965855	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55922072	GTGGAGAATGAATGG[A/G]TAAGGGAGATCACAG	4067
rs188977456	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55895992	GGAAATTTGGTGTAC[A/T]TACCAGGTGCACTTT	4067
rs188981231	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55902658	AGCTGAAAATTCCTT[A/G]TTACTTAAATGTTAT	4067
rs189009558	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55994947	TACTGTGTTATAATC[A/G]TACACTCCTTTCTTT	4067
rs189026325	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55957691	CTCACACCTGTAATC[C/T]TGGCACTTCGGGAGG	4067
rs189043488	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55932953	AGCAATAGACACGGG[A/C]GACTACTAAAGTGGG	4067
rs189050893	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55939260	AGATCAGCTGTGCCT[C/G]AGCAGTGAGGCCATG	4067
rs189096754	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:56002280	AACAATTAGCCAGGC[A/G]TGGTGGCAGGCGCCT	4067
rs189123245	snp	C/T	0.00318978	0.0398085	intron-variant	LYN	GRCh38.p7	8:55937637	GATAATGGTAAGGCA[C/T]TGCTAGATTTTATGA	4067
rs189172129	snp	C/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55971137	GAAATTCAAGTGTGC[C/T]CTGAAATGCCAACAT	4067
rs189188315	snp	C/G	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55952356	TTGAGGTCAGGAGTT[C/G]GAGACCAGCCTGGCC	4067
rs189198351	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55976466	TGAGCCCCCTCACCC[A/T]CTTGGTGTGGCCCGC	4067
rs189205335	snp	A/C			intron-variant	LYN	GRCh38.p7	8:56008084	AGATCGCTCCACTGC[A/C]CTCCAGCCTAGGTGA	4067
rs189264647	snp	C/T	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:55881583	TTGGTGACTGGGCCT[C/T]TTTGGATGTAAATGT	4067
rs189279603	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55920141	AAATAATTCAGCAGA[C/T]TAATTGTGGGAAGGC	4067
rs189321885	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55956330	AGATTAAGTGCAGAC[A/G]TGACTTGCTGAGTTT	4067
rs189421007	snp	C/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55925004	CCACCACCACACCTG[C/G]CTAATTTTTATATTT	4067
rs189426879	snp	A/C	0.0170251	0.090679	intron-variant	LYN	GRCh38.p7	8:55942696	AGGCTGAGGCAGGAG[A/C]ATCGCTTGAACCTGG	4067
rs189454292	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55886078	ATTTTGAAATTCCCC[A/G]TCATGGAAAGTGTTA	4067
rs189458624	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55907259	TTACTCAACCAAAAA[A/T]ATGAGACACTGATAT	4067
rs189472226	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55997015	AAAATACAAAAATTC[A/G]CCAGGCATGGTGGTG	4067
rs189524866	snp	C/T	0.00517822	0.0506191	intron-variant	LYN	GRCh38.p7	8:55910682	ACATAATTTCTAAGA[C/T]ATATTCAGGTTTCAC	4067
rs189548561	snp	A/G	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55947198	AGGTTGCAGTGAGCC[A/G]AGATTGCACTATTGC	4067
rs189570381	snp	A/G	0.000864942	0.0207779	intron-variant	LYN	GRCh38.p7	8:55946541	TTTTCTTTACTATTA[A/G]AGCTTCTATAAAGTG	4067
rs189588998	snp	A/G			intron-variant	LYN	GRCh38.p7	8:56001057	CGAGTACTCACAGAA[A/G]GGGGTGGGGAGCTGC	4067
rs189595131	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55929391	GTTTCAACAGCTACC[A/G]GATCTGTGTATGTGT	4067
rs189597454	snp	C/T	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:55893652	CTTCTTGGATACTCA[C/T]TACTCATGAATATGC	4067
rs189604499	snp	C/T	0.00438332	0.0466095	intron-variant	LYN	GRCh38.p7	8:55911397	AAAGTGTTGGGATTA[C/T]GGGCGTGAGCCACCG	4067
rs189605817	snp	C/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55982301	AAGTGCTTCAGATTT[C/G]GTTTTGTTTTTTTTT	4067
rs189607522	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55903126	TGCTGGGATTACATG[C/T]GTGAGCCACTGCGCC	4067
rs189608901	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55930324	TTCATAATAATTTCT[A/G]TTATGTTACATGCAT	4067
rs189609929	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55963691	ACTTTTCACGTGTTT[A/G]TTACTCATATGAATT	4067
rs189611666	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55920362	TAACAATTTTGTTTG[C/T]GCAGAATGTCACAGC	4067
rs189615357	snp	A/C	0.00115517	0.0240052	intron-variant	LYN	GRCh38.p7	8:55947587	TTCTGCTGATGGATT[A/C]TTACAGGTGTTCTCT	4067
rs189631397	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55884594	CCTAGTAGCTGTGAT[G/T]ACAGGCGCCCGCCAC	4067
rs189652757	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55924876	TGAGATGGAGTCTCT[C/G]TGTTGCCCAGGCTGC	4067
rs189700698	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55959048	TACTGTTTTCTACTT[C/T]GGCTGCACCATTTTA	4067
rs189712616	snp	A/T	0.00557542	0.0525036	intron-variant	LYN	GRCh38.p7	8:55943489	GCTGAGGAAGAAGAA[A/T]TGCTTGAACCCAGAG	4067
rs189746351	snp	A/G	0.00279162	0.0372561	intron-variant	LYN	GRCh38.p7	8:55908510	TCAGCCTCCCAAAGT[A/G]TTGGGATTCCAGGCC	4067
rs189749844	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55994714	AGCCAGCTTTGGCTT[A/C]TTTGGGTTCTTGGCC	4067
rs189754427	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55926645	CACAGCAGGTAACGG[C/T]CTGCCCTTGATAATT	4067
rs189754431	snp	A/G	0.00517822	0.0506191	intron-variant	LYN	GRCh38.p7	8:55961423	TCCTTAGCACTGAAT[A/G]AAAATCATGCCTTTA	4067
rs189809905	snp	C/G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55929679	GGGAGGCCTGGAGAG[C/G/T]TGCTACTGGCATCCA	4067
rs189837159	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55896275	ACTCTCATCTCTGAA[A/G]AAAAAAGAAAAGAAA	4067
rs189843982	snp	C/G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55892738	CTGACACAGTTCTTT[C/G/T]TAACAGGATTCGAGG	4067
rs189859910	snp	C/T	0.0123036	0.0774623	intron-variant	LYN	GRCh38.p7	8:55967512	GTAGAGATGGGGTTT[C/T]GCCATGTTGGCCAGG	4067
rs189884377	snp	A/C	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:56005019	CTAACTCCTGGGTCA[A/C]CTGATCCTCCCTCCT	4067
rs189910242	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55906562	GAGTTTCACCATGTT[A/G]CCCAGGCTAGTCTTG	4067
rs189994944	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55982746	TCTTGACTTCCTCCC[C/T]TCCAAGACTCTGTCC	4067
rs190003090	snp	C/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:56008661	CAGCTTCTGAATTAC[C/G]CTGAGACATTTGACC	4067
rs190016687	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56005680	CTCTTTTTTGTTTTG[G/T]GATGAATTACAGAAA	4067
rs190053629	snp	G/T	0.0023933	0.0345097	intron-variant	LYN	GRCh38.p7	8:55914922	AACTCAACTTGAAAT[G/T]GTCTCTTAGCCATCT	4067
rs190059524	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55886408	ATGCACCACCATGCC[C/T]GGCTAATTTTTGTAT	4067
rs190069497	snp	G/T	0.00279162	0.0372561	intron-variant	LYN	GRCh38.p7	8:55951012	CTTTGGGAGGCTGAG[G/T]CGAGAGGATCACTTG	4067
rs190104677	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55987974	CATCATCATCAAAGT[A/T]TAGATTTCACTATTT	4067
rs190215539	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55903663	TTTATTGAGACCTTC[C/G]TTTTGAAAGTAACTT	4067
rs190243006	snp	A/G			intron-variant	LYN	GRCh38.p7	8:56001774	ATCTGACACCTGATA[A/G]ACATACAATCTCATA	4067
rs190261128	snp	A/G	0.0107246	0.0724382	intron-variant	LYN	GRCh38.p7	8:55964903	CTTGCACCCTAAAAA[A/G]GGGACCGTCCACTCC	4067
rs190354867	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55878197	TTCAGCAAGTATAAA[C/T]GCAGCCTAAGAAGTG	4067
rs190358988	snp	A/G	0.00795532	0.062565	intron-variant	LYN	GRCh38.p7	8:55900078	ATCTAATGCGCTGCC[A/G]CTCGAACTTCAGGAA	4067
rs190398943	snp	A/G	0.00318978	0.0398085	intron-variant	LYN	GRCh38.p7	8:55953463	ACCAGCCTGGCCAAC[A/G]TAGTAAAATTCTGTC	4067
rs190399310	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55978526	AGGGGTCTGGGGCTA[A/G]AGGCTTCAAGGAGGC	4067
rs190409338	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55962722	TGATGAAATTGGAGT[C/T]CATGTTAGTCCATTT	4067
rs190419346	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55916546	TGTGAGCTACACTGC[A/C]ACAACTGTTTTAGAT	4067
rs190420543	snp	A/C	0.0119091	0.0762411	intron-variant	LYN	GRCh38.p7	8:55944103	AAAAAAAGGAAGTGG[A/C]GATAAAGAGTGGATA	4067
rs190421392	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56007670	TAAGTTAAAGGCAGA[A/G]GATCTCAAAGTTTAT	4067
rs190429040	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55936115	GATACTGGAATGCAA[C/G]TGTGTAGGGAACATA	4067
rs190435141	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55990972	ACTCTGCCCAGCTTA[A/T]GTGTGTGCCTATTTA	4067
rs190442531	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55970623	CACTGCCACTTCTTC[C/T]CTCACACCCTCTTTT	4067
rs190447484	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55998009	GAATGGTGTGAACCC[A/G]GGAGGTGGAGCTTGC	4067
rs190449759	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55891543	GGCTTGATGGGGGAG[G/T]GAATGGGAAGTTACT	4067
rs190517646	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime	LYN	GRCh38.p7	8:55877502	AGAAGGCAGAGCATC[A/G]CCTTGTTCCACTATA	4067
rs190519043	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55956489	TTATTTAAAGTGATC[C/T]AAAAGTTTAAATGGA	4067
rs190529618	snp	A/C	0.00318978	0.0398085	intron-variant	LYN	GRCh38.p7	8:55897902	TGCGTGACAGTGAGG[A/C]CCTGTCTCACAAACA	4067
rs190536658	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55916475	TGCTCTGGAAGGGTG[C/T]GTGCGAATATGGTTC	4067
rs190548719	snp	G/T	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55993685	TGTAAAGGATGTGAA[G/T]CAGTGTTTGGTGTAT	4067
rs190617201	snp	C/G	0.00478085	0.0486577	intron-variant	LYN	GRCh38.p7	8:55959416	TTTAATGGAACCTAT[C/G]TCAGAGGGATTACAT	4067
rs190637347	snp	A/G	0.0150606	0.0854603	intron-variant	LYN	GRCh38.p7	8:55904736	GCCTTGTAACAGAGC[A/G]AGACTCCATCTCAAA	4067
rs190641760	snp	C/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55956750	AAGATCCAGGGACTT[C/G]TGCGTTCTCTTCCCG	4067
rs190651608	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55941026	AATGTTTTCATAAGT[A/G]TCTTCTCTCCCATAA	4067
rs190664628	snp	C/T	0.00318978	0.0398085	utr-variant-3-prime, downstream-variant-500B	LYN	GRCh38.p7	8:56011864	TTTTTGTGTACACCC[C/T]CCTGCTTGCATTTTA	4067
rs190668315	snp	A/T	0.00716266	0.059414	intron-variant	LYN	GRCh38.p7	8:55920936	TCCTGACCTCAGGTG[A/T]TCTGCCCGCCTTAGC	4067
rs190668613	snp	A/G	0.0023933	0.0345097	intron-variant	LYN	GRCh38.p7	8:55994106	ATTTACTTAGCCGTA[A/G]TAAATAGACCACCTT	4067
rs190668636	snp	G/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55895041	CTGGTCTTGAACTCC[G/T]GGTCTCAAGCGATCT	4067
rs190675082	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55940547	CGCCCAGCTAATTTT[C/T]GTATATTTAGTAGAG	4067
rs190683196	snp	A/G	0.00438332	0.0466095	intron-variant	LYN	GRCh38.p7	8:55974081	ATATTTTGTTGTTTA[A/G]TACCTCTTACAGATA	4067
rs190696306	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55974665	TTCTAGAATATTTGC[C/T]AATATCATCCAAAGT	4067
rs190763407	snp	G/T	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55910334	TTGTATATGGTAAGA[G/T]ATATGGAGTCCAGTT	4067
rs190807691	snp	A/C	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55973410	TTGTATTAAATTAAG[A/C]AATTTAGTGCTTTTT	4067
rs190813988	snp	C/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55978060	AAAGCCAAGAAGCAC[C/T]TGAAGGAGTTCAGCC	4067
rs190864163	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55887958	AGCAATGGAATGAAG[C/G]CAGTGGGACTGCAGA	4067
rs190892461	snp	C/T	0.00636936	0.0560724	intron-variant	LYN	GRCh38.p7	8:55921496	TCCTGGGGCTTGGGA[C/T]GAAATTCCAAATTGA	4067
rs190913209	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55983622	CATCCAAAGGGCACC[C/T]ATCTCTCAGCATCTT	4067
rs190923583	snp	A/G	0.00358779	0.0422022	intron-variant	LYN	GRCh38.p7	8:55883681	ATCAGTGAGAGCATC[A/G]TTTAAGTGAAAATAT	4067
rs190959752	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55957116	TGGACTCAATTATTT[A/G]CTACACTATTTCTAA	4067
rs191039821	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55984286	TGTCTAGACTCCGGC[C/T]ACTCCGAAGCTTCTA	4067
rs191043930	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55965522	ATAAGTAATTTTTAT[A/G]AAGAACACCTTTTTT	4067
rs191055250	snp	C/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55935289	TCAGATAGAGAAAGC[C/T]GTGCTATGCAGCTTG	4067
rs191075937	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56003153	CTAGCCCCACCTCCC[A/G]GGTTCACGCCGTTCT	4067
rs191169326	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55881983	TGAAGAAATAGAGCT[G/T]GTCCCTAAGGTGTTT	4067
rs191295022	snp	C/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55895785	GTTGCAAGGATTAAA[C/T]GGGGTAATGTACCTG	4067
rs191296843	snp	A/C	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55926374	GCCTGTTGACTATGC[A/C]TGTATAGATGTGTAA	4067
rs191302020	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55912885	TTCTTAAAATGGCCC[A/G]TGTGTAAAAAGTTTA	4067
rs191334078	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55997813	GACATGGCCAGGCGC[A/G]GTGGCTCACGCCTGT	4067
rs191337216	snp	C/T	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:55949099	TTTCTGCTGAGGACT[C/T]GAGCATGGTGCTGAA	4067
rs191354383	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55960471	TGCCTGTCAGTCAGC[A/G]AGCTCCTTCTTCACT	4067
rs191362796	snp	A/G	0.00398564	0.0444627	intron-variant	LYN	GRCh38.p7	8:55932860	TAAGTGAATTAATGC[A/G]GGAACAGAAAACCAA	4067
rs191365256	snp	C/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55985866	ACCTTGACCTTCAGT[C/T]TTTTAATATACTAAG	4067
rs191377105	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55966271	TACTTTTCATCTAGC[C/T]TCCCCTAATTTTATC	4067
rs191437637	snp	C/G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55935413	ACCATGGTATGTAAG[C/G/T]CAAAAAATCTTAGTT	4067
rs191445305	snp	C/T	0.00358779	0.0422022	intron-variant	LYN	GRCh38.p7	8:55891093	TGCGGTGGCTCATGC[C/T]TGTAATCCCAGCACT	4067
rs191453339	snp	A/C	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55910150	AAGCTTTTTAGTTTA[A/C]GTAAGTCTCATTTGT	4067
rs191456262	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55970249	GCTCCTCTTCTCGCT[C/T]CTTCTTGTTGGATGT	4067
rs191477502	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55963383	CAGAGCTGTACTTAG[A/G]GAGATGTGGGCCCCA	4067
rs191486760	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55972190	CACTGGGAGAGTCAC[A/G]GGTCAGCAGCAGCCG	4067
rs191487244	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55946224	CCTGCCCAGAACCTC[G/T]CTCCCTTCCTGCCAC	4067
rs191487293	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55991296	CTTTGGGGTCAGAAC[A/G]TTGGGTAAGACCTTA	4067
rs191489312	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56006840	CACATGTAATCTTAG[C/G]GTCTGGTTGAGGTCC	4067
rs191495031	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55955975	ATGAATAATGCTGTA[C/T]GAATGTTCACATACA	4067
rs191517657	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55981526	GTGTGTTTAAAAAAA[A/T]TTTTTTTAATATAGA	4067
rs191520039	snp	A/G	0.00398564	0.0444627	intron-variant	LYN	GRCh38.p7	8:56007957	AACCCCGTCTCTACT[A/G]AAAATACAAAAATTA	4067
rs191520679	snp	A/C	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:56008668	TGAATTACCCTGAGA[A/C]ATTTGACCACATTAA	4067
rs191522592	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55991998	TACGTGATTAGTCTC[A/G]TTTTTGGTAATAGGG	4067
rs191523336	snp	A/G	0.00755907	0.0610114	intron-variant	LYN	GRCh38.p7	8:55907758	GTGGTCCCAGCTACT[A/G]GGGAGGCTGAGGTGG	4067
rs191552550	snp	A/C	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55943231	ACATGTATACCACCC[A/C]TAGCCTGCTTTCTAT	4067
rs191581830	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55977686	GGGAGGCTGAAGTGG[A/G]AGGGTTGCCTGAGGC	4067
rs191618821	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55948397	ACTGGGTTCATGGGC[A/C]CAGCCTAGCTTGAGT	4067
rs191626844	snp	C/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55912475	TTATGCCTGTAATCC[C/T]GCACTTTGGGAGGTC	4067
rs191660344	snp	C/T	0.00676609	0.0577691	intron-variant	LYN	GRCh38.p7	8:55984846	CATGATGTAGATTTG[C/T]TTTCAGAAGTTACTC	4067
rs191705533	snp	G/T	0.00398564	0.0444627	intron-variant	LYN	GRCh38.p7	8:55927179	AGTGTATAATGACAT[G/T]TATTCACCATTACAG	4067
rs191720067	snp	C/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55952641	TCCTTGTGAATAATT[C/T]TCCCAGTCCTTCCCA	4067
rs191752701	snp	A/G	0.0023933	0.0345097	intron-variant	LYN	GRCh38.p7	8:55990108	GCCAGGCATGGTGGC[A/G]GACACCTGTAGTCCC	4067
rs191854005	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55919596	TTTAGCTTCCTGGTC[C/T]CAGAAAGAAAAAACA	4067
rs191858734	snp	A/G	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:55939172	GCTCATCCCCATGTC[A/G]CATGGAGGACCTCTG	4067
rs191863340	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55931552	TGTAGATGAACATTG[C/T]GGTAGTTTAGCCTAT	4067
rs191905755	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55965986	AAAAATTAGCCAGGT[A/G]TGGTGGTGGGCACCT	4067
rs191933795	snp	A/G			intron-variant	LYN	GRCh38.p7	8:56003504	ACCCTGTCTCTACAA[A/G]AAATACAAAAAAAAT	4067
rs191938939	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55890604	CCCAAATAACTGAAT[A/G]TGGGGTCTCAGAGAT	4067
rs191940709	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55916028	CATTGTTTTAAAAGC[A/G]TATAAAATAATGGTA	4067
rs191956117	snp	A/G	0.00398564	0.0444627	upstream-variant-2KB, missense	LYN	GRCh38.p7	8:55879570	GACGCGAGAGGTGTA[A/G]TCGATGTGCCTGCGA	4067
rs191960974	snp	C/G	0.00795532	0.062565	upstream-variant-2KB	LYN	GRCh38.p7	8:55877183	TCTCCAGTGGGCACG[C/G]CACAGCCTCTGGTGC	4067
rs192019784	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55902108	TGTCTCCTGGGTTCA[A/G]GCAATTCTCCCACCT	4067
rs192024410	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55917907	TTAATTTAAACTTAA[A/T]GACATGTTGTATTCA	4067
rs192045853	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55894587	GCCCAGGCTGGAGTT[C/T]ATTGGCGCTATCTTG	4067
rs192061493	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55930954	CCATGCATGGCTACT[C/T]TCTAAGTTCTTACTC	4067
rs192112335	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55924751	CTAGAGTGAGTTTAC[A/C]GTGACTCTCCAGTTC	4067
rs192113718	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55995080	AGAGGCAGGGCTCCT[C/T]TCTCCCAGCCGCCAC	4067
rs192151738	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55975127	GTGCCGCTGTGGATT[C/T]AGGGGCCACATAGTG	4067
rs192159362	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55958487	TAAATACACGTGACA[C/T]AAAATTTGTGTTTTA	4067
rs192173598	snp	A/G	0.0498117	0.149749	intron-variant	LYN	GRCh38.p7	8:55942421	TATATATATGTGTGT[A/G]TATATATATATGTGT	4067
rs192200345	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55995827	AAAGGAGCTTGGACC[A/G]CATTCTTTGTTTCCA	4067
rs192229657	snp	C/T	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:55942512	TAGTGAGAGGCTGGG[C/T]GCGGTGGCTCACGCT	4067
rs192246101	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55976187	TTGAAATTAGCCAGG[C/T]TTGGTGGTGCGTGCC	4067
rs192251090	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55897110	ACGATGTTACTCACC[C/T]GAACGCTGGCTTTAT	4067
rs192254336	snp	C/T	0.00398564	0.0444627	intron-variant	LYN	GRCh38.p7	8:56004221	ACAGGTGTGAGTCAC[C/T]GCACCCGGCCTAAAT	4067
rs192328723	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55917225	GGATCTTGCGCTGTC[A/C]CCCAGGCTGGAGTGC	4067
rs192345790	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55954371	TAATAGAAAGCCTCA[A/G]TGTATTACAATTTGA	4067
rs192349759	snp	C/T			intron-variant	LYN	GRCh38.p7	8:56004630	AATTCCCCATGCCTG[C/T]GGGTGCTCCTCAAAG	4067
rs192353776	snp	C/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55987667	GTGATCCACCCACCT[C/G]GTCCTCCCAAAGTGC	4067
rs192364440	snp	A/T	0.00199481	0.0315187	upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55878429	TGAATCCTATTCTTA[A/T]TTGCCACACACGTTT	4067
rs192368560	snp	A/C	0.00716266	0.059414	intron-variant	LYN	GRCh38.p7	8:55967343	TTTTGGAAACAGAGT[A/C]TCACACTGTTGCCCG	4067
rs192416511	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55911835	TGGTTTTAAACTTCA[A/G]CACCTGGTGCCCTTT	4067
rs192542036	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55999193	AAGCACTTTCTTGAA[A/G]TTCCTAAGCATTGTT	4067
rs192628435	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55884153	CGCCCAGCCTGGAGT[A/G]CAGTGGTGCAATCTC	4067
rs192655950	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55884706	GTGAGCCCGCCTCGG[C/T]CTCCCAAAATGCTGG	4067
rs192662209	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55959172	GGTTGGCTTTTGTGA[C/T]AGTTGTCATTTTAAT	4067
rs192676586	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55924905	GCAGTGCGGTGGTGC[A/G]ATCGTGGCTCACTGC	4067
rs192681911	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55904857	TTATTAGACTGCGCA[C/T]TTTACCCTTTTTCAA	4067
rs192690497	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55996872	TGGTGGCTCATGCCT[A/G]TAATTTCAGCACTTT	4067
rs192693804	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55923233	GGCCTCTAAGGTACT[A/G]ATCCTTTCTGAGAGT	4067
rs192701216	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55941604	TTACACATCTTTGCC[A/G]CAAGAATACGAGCAG	4067
rs192720391	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55937077	TCAGGCAATAGACCC[A/T]GCAGTTGACTTCAGC	4067
rs192738485	snp	C/T	0.0023933	0.0345097	intron-variant	LYN	GRCh38.p7	8:55901461	GCTTTAGACTCCTTC[C/T]TGGGCTCATGCATGG	4067
rs192748925	snp	C/T	0.00478085	0.0486577	intron-variant	LYN	GRCh38.p7	8:55971029	GCAATGCCCATCCTT[C/T]CAGTAAAGGTGTGTG	4067
rs192758378	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56000455	GGATTTCGGCCAGGT[A/G]CAGTGGCTTACACCT	4067
rs192779879	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55928302	AGGCAAGCGCCACCA[C/T]GCCCGGCTAGTTTTT	4067
rs192784965	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55902475	TGGAATTACAGGTGC[A/G]CTCCACAACGCCCAG	4067
rs192795615	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55963222	TGCATGAGCTCTAGG[A/G]TGAGTGGGAGTGGAT	4067
rs192826625	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55979981	AGGCCTGCAGCTGAC[A/T]GCCCTCCAGAGGCCC	4067
rs192834053	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55909545	CTTTGCTATTCTGAA[C/T]AGTGCTCCAATAAAC	4067
rs192871423	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55971409	TCTGATAAACTTGGG[C/T]CATACTTACACGGAT	4067
rs192905263	snp	G/T	0.0115144	0.0749975	intron-variant	LYN	GRCh38.p7	8:55884348	GACCCCAAGTGATCT[G/T]CCCGTCTCGTCCTCA	4067
rs192941922	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55988728	TCTAAGACAGGTTGC[A/G]TTTTCAGTTCCAGTT	4067
rs193006985	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55945620	CAGCATCTATCTTAC[A/G]AGAGGCCCAGAGGCC	4067
rs193036267	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55889252	AGACCAGGCTGTAAC[C/T]CCAGGCAGGAGTACA	4067
rs193072295	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55991983	CTGACATCGTCTCTT[C/T]ACGTGATTAGTCTCA	4067
rs193082442	snp	A/G	0.0138799	0.0821421	intron-variant	LYN	GRCh38.p7	8:55954861	ATAAATAAATAAATA[A/G]ATAAATAAATAAAAG	4067
rs193141623	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55933571	TCACTTATCCTCTCA[C/T]GCCAAGCCCAGTGAT	4067
rs193150792	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55957904	AGTGAGCTGAGATTG[C/T]GCCGCTGTCACCAAA	4067
rs193152361	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55896143	GACGTGGTGGCATGC[C/G]CCTGTCATCCTAGCT	4067
rs193157577	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55906045	CTTTCTTTTTCCATA[C/T]AGTAGTTCATCTGAT	4067
rs193176471	snp	C/T	0.00438332	0.0466095	intron-variant	LYN	GRCh38.p7	8:55967574	GCCTGCCTCAGCCTC[C/T]GAAAGTGCTAGGATT	4067
rs193184687	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56005225	CCTATAAGGGGAGTC[A/G]TACAGTTTTGCCCTA	4067
rs193292005	snp	A/G	0.00716266	0.059414	intron-variant	LYN	GRCh38.p7	8:55914365	ATGAAATATACTGAG[A/G]TGGCCCCCATACTTT	4067
rs193297560	snp	A/C	0.00138342	0.026264	intron-variant	LYN	GRCh38.p7	8:55950599	GTGGCTTTATTTGCC[A/C]CATTGGATTTCTTGT	4067
rs193299684	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55974897	TGGCAAGTGGAAGCC[A/G]CAGGTGATTGACATG	4067
rs199545095	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55902263	TCTGCCCATTTTTGC[C/T]TCCCAAAGTGCTGGG	4067
rs199558188	in-del	-/ATA			intron-variant	LYN	GRCh38.p7	8:55908911	GTTGCTGCAAAATAC[-/ATA]ATTTTATTCTTTTTT	4067
rs199581140	in-del	-/AC			intron-variant	LYN	GRCh38.p7	8:55911081	TATATATATATACAT[-/AC]ATATATATATATATA	4067
rs199629503	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55891950	ATATTGAAATGGCTG[G/T]GATGTGGGAGAGGGA	4067
rs199651695	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55946754	GTCCCCATTGCCTCC[A/G]CCCCCAGCCGCTGGC	4067
rs199655758	in-del	-/AAAT	0.293294	0.246223	intron-variant	LYN	GRCh38.p7	8:55954836	TGAGACCCTGCCTCA[-/AAAT]AAATAAATAAATAAA	4067
rs199691085	in-del	-/C	0.0023933	0.0345097	downstream-variant-500B	LYN	GRCh38.p7	8:56012737	AAAAAACCAAAAAAA[-/C]AAAAAAACCCTTCCC	4067
rs199773007	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55908993	CCATTGTGTATGTAT[A/G]TATATATATATATAT	4067
rs199851768	in-del	-/T			intron-variant	LYN	GRCh38.p7	8:55896100	TTAGGGGTAAAGCAA[-/T]TTAAAAAAAAAAAAC	4067
rs199958251	snp	C/T	5.00705e-05	0.00500327	intron-variant	LYN	GRCh38.p7	8:55946497	TTCAAACTAAAGGTA[C/T]GTTTTCATAGCAACA	4067
rs199968692	snp	G/T			intron-variant	LYN	GRCh38.p7	8:56002573	CACCACTGCAGTCTA[G/T]CCTGAGCGACAGGAA	4067
rs199976380	in-del	-/CTTTA	0.0244538	0.107838	intron-variant	LYN	GRCh38.p7	8:55912906	AAAAAGTTTATTCCC[-/CTTTA]CTTTACTTTTATATA	4067
rs199978964	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55891306	GCAGTGAGTCGAGAT[C/G]CCGCGACTGCACTCC	4067
rs200044726	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55896104	GGGGTAAAGCAATTA[A/T]AAAAAAAAAACAAGT	4067
rs200107802	snp	A/G	3.29468e-05	0.00405861	synonymous-codon	LYN	GRCh38.p7	8:55969772	AGTGCTGCTTCCAAA[A/G]CTCATTGACTTTTCT	4067
rs200111319	snp	A/G			intron-variant	LYN	GRCh38.p7	8:56005571	AGGCACGTTGGTTGC[A/G]CTTTCTTCCTCTTGG	4067
rs200221923	in-del	-/GTTTT			intron-variant	LYN	GRCh38.p7	8:55906365	GTTTTGTTTTGTTTT[-/GTTTT]TGACAGAGTTTCAAT	4067
rs200238523	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55913224	TTACCAAATAATTCA[C/T]ATTGAAATATAAATA	4067
rs200240180	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55902026	CTTTCTTTTTTTTTT[G/T]AGACGAGTTTCACTC	4067
rs200252698	snp	C/T	6.60447e-05	0.00574613	intron-variant	LYN	GRCh38.p7	8:55953994	GGATGGGTAAGTGTG[C/T]GGCTCGGGGATCTAT	4067
rs200287325	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55954977	ATGGAATGTGCGGTT[A/G]TTTCTGGAAAGAGTA	4067
rs200293439	in-del	-/G			intron-variant	LYN	GRCh38.p7	8:55986193	ACCAGAATCCCCCCC[-/G]CAAAAAAAAACGCTA	4067
rs200299276	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55892312	GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG	4067
rs200328994	in-del	-/AGAG	0.00676609	0.0577691	intron-variant	LYN	GRCh38.p7	8:55917189	TAAAAAAAAAAAAAA[-/AGAG]AGAGAGAGAGAAAGA	4067
rs200330287	in-del	-/AA/AAA	0.0995987	0.199992	intron-variant	LYN	GRCh38.p7	8:56002426	CCATCTTAAAAAAAT[-/AA/AAA]AAAAAAAAAAAGAAT	4067
rs200330540	in-del	-/T	0.00993419	0.0697739	intron-variant	LYN	GRCh38.p7	8:55916864	ATTTTGAGACTGCTA[-/T]TTTTTTTTTCTCTTT	4067
rs200336718	snp	A/C/T	1.65228e-05	0.00287422	intron-variant	LYN	GRCh38.p7	8:55999572	TTACTTAGCTATTTA[A/C/T]AATCAAGCTGTATAA	4067
rs200346825	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55909991	TGTGTGTGTGTGTGT[G/T]TCTTTTTTTTTTTTT	4067
rs200375367	in-del	-/TTC			intron-variant	LYN	GRCh38.p7	8:55909140	TCATGGCGAATTTGC[-/TTC]TCTGCTAAGTAGGAA	4067
rs200445493	in-del	-/G			intron-variant	LYN	GRCh38.p7	8:55906746	AAAAAGAGAGAGAGA[-/G]GAGAGAGAGAGAGAA	4067
rs200465646	snp	A/G	0.00441245	0.0467627	intron-variant	LYN	GRCh38.p7	8:55951944	GAGATATAAACATTT[A/G]CTTACACTTTTCCCC	4067
rs200500233	snp	A/G	1.65061e-05	0.00287277	synonymous-codon	LYN	GRCh38.p7	8:56010089	CACAGCCACGGAAGG[A/G]CAATACCAGCAGCAG	4067
rs200529569	snp	A/G	0.000653984	0.0180711	intron-variant	LYN	GRCh38.p7	8:55966911	GGGTGAGTTCCTCCC[A/G]CTGCCCAGAGCTTGC	4067
rs200572975	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55904006	AGTAAGACAGAGTCT[A/C]AAAAAAAAAGTGTTT	4067
rs200582459	in-del	-/A			downstream-variant-500B	LYN	GRCh38.p7	8:56012727	TCTCAAAAAAAAAAA[-/A]CCAAAAAAACAAAAA	4067
rs200620709	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55895034	GCCCAGGCTGGTCTT[A/G]AACTCCTGGTCTCAA	4067
rs200632912	in-del	-/ACAGCA	0.00636936	0.0560724	intron-variant	LYN	GRCh38.p7	8:55920373	TTTGTGCAGAATGTC[-/ACAGCA]ACATTTCTTAAGTGT	4067
rs200640956	in-del	-/A			intron-variant	LYN	GRCh38.p7	8:55891304	TTGCAGTGAGTCGAG[-/A]TCCCGCGACTGCACT	4067
rs200715203	in-del	-/TAATATAG	0.00676609	0.0577691	intron-variant	LYN	GRCh38.p7	8:55919399	ATATGAATGCTCTGT[-/TAATATAG]TGCTTTTCATAGAAA	4067
rs200804081	in-del	-/AAG	0.0901694	0.192235	intron-variant	LYN	GRCh38.p7	8:56003685	TCTCAAAAAAAAAAA[-/AAG]AAGAAGTCATATCAT	4067
rs200808357	in-del	-/TCTC			intron-variant	LYN	GRCh38.p7	8:55910631	CTTTGGTATTTGTGC[-/TCTC]TTTTGGTTCCATATG	4067
rs200831559	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55909452	TAATCCCACAGATGG[C/T]AGATTCGCCCCATTG	4067
rs200930377	in-del	-/AA			intron-variant	LYN	GRCh38.p7	8:56001759	AGATTATGTATATAA[-/AA]TCTGACACCTGATAA	4067
rs200982543	in-del	-/A			intron-variant	LYN	GRCh38.p7	8:55896103	AGGGGTAAAGCAATT[-/A]AAAAAAAAAAACAAG	4067
rs200994129	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55944445	TATAGATTTTGTAGG[G/T]TTTAAAACACAAGTT	4067
rs201017621	in-del	-/AT			intron-variant, downstream-variant-500B	LYN	GRCh38.p7	8:55968263	AATATATATATATAT[-/AT]TTATTTTTTTGAGAC	4067
rs201069098	in-del	-/TC			intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55924064	TTTTTTCTTTTTCTT[-/TC]TTTTTTTTTTTTATT	4067
rs201107678	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55938902	TGCGCGAGTCTTTTA[A/G]CCTTTCTGAGCCTCA	4067
rs201139655	in-del	-/C	0.0678174	0.1712	intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55924065	TTTTTCTTTTTCTTT[-/C]TTTTTTTTTTTTATT	4067
rs201201305	snp	C/T	0.000115459	0.00759712	missense	LYN	GRCh38.p7	8:55966759	GTGAAAACCCTGAAG[C/T]CAGGAACTATGTCTG	4067
rs201223055	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55932413	AATTATATATATATT[G/T]TTTGTTTGTTTGTTT	4067
rs201264277	in-del	-/T			intron-variant	LYN	GRCh38.p7	8:55977196	GTCTCAAAAAAAAAA[-/T]AAAAATAAAAATAAA	4067
rs201276146	snp	A/G	1.64751e-05	0.00287007	missense	LYN	GRCh38.p7	8:55999487	TCACTATTAAGTCTG[A/G]TGTGTGGTCCTTTGG	4067
rs201286024	in-del	-/TA			intron-variant	LYN	GRCh38.p7	8:55932400	ATCTTTTAAAACAAT[-/TA]TATATATATATTTTT	4067
rs201287071	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55909993	TGTGTGTGTGTGTGT[C/T]TTTTTTTTTTTTTTT	4067
rs201314597	in-del	-/TA	0.115088	0.210473	intron-variant	LYN	GRCh38.p7	8:55942420	GTATATATATGTGTG[-/TA]TATATATATATGTGT	4067
rs201324066	in-del	-/ATA	0.00755907	0.0610114	intron-variant	LYN	GRCh38.p7	8:55931182	ATTATATTTTAAAAT[-/ATA]ATATGTAACTCGTAC	4067
rs201371184	in-del	-/TGTGTCTTT			intron-variant	LYN	GRCh38.p7	8:55909988	TTGTGTGTGTGTGTG[-/TGTGTCTTT]TTTTTTTTTTTTTTG	4067
rs201417033	in-del	-/ATATAC			intron-variant	LYN	GRCh38.p7	8:55887572	AATATATATATATAT[-/ATATAC]ACACACACACACACA	4067
rs201419386	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55997530	CAGCTCTCTGGGGTC[C/T]CTTTTACAAGGGCAC	4067
rs201436721	in-del	-/C	0.00755907	0.0610114	intron-variant	LYN	GRCh38.p7	8:55985319	ACCCACCTGCTCTTG[-/C]CCCCCACATCCTTAG	4067
rs201517305	in-del	-/AA	0.499234	0.0195537	intron-variant	LYN	GRCh38.p7	8:55887561	TAAAAATATAAATAT[-/AA]ATATATATATATATA	4067
rs201629502	in-del	-/AG/G			intron-variant	LYN	GRCh38.p7	8:55956118	TGCTCATTAAAAAAA[-/AG/G]GAATGACTTGGCTTC	4067
rs201631196	snp	A/G	0.0588605	0.161139	intron-variant	LYN	GRCh38.p7	8:55927843	TCTGTCCCAAGGGGG[A/G]AAAAAAAAAGAAAGA	4067
rs201652374	in-del	-/A			intron-variant	LYN	GRCh38.p7	8:55895459	TTGGGGTGTCTGAGG[-/A]GCAGCATGATGTCGT	4067
rs201666275	snp	C/G/T	3.29708e-05	0.00406011	intron-variant	LYN	GRCh38.p7	8:55999401	CCCAAGTAAGAACCA[C/G/T]ATATCTTCTTCCTTA	4067
rs201680249	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55985177	GGGGAGGAACTGTAC[C/T]TCTCTCACTGCTCTA	4067
rs201704009	in-del	-/CGC			intron-variant	LYN	GRCh38.p7	8:55886395	AGGCATGCACCAATG[-/CGC]CACCACCATGCCCGG	4067
rs201708631	in-del	-/TATAT	0.00755907	0.0610114	intron-variant	LYN	GRCh38.p7	8:55931142	TTATATATAATAAAA[-/TATAT]TATATTTTTAAATAA	4067
rs201723253	in-del	-/T	0.0134861	0.0810011	intron-variant	LYN	GRCh38.p7	8:55959606	ATTTTTGCTTTTTAA[-/T]TTTTTTTTATTTTGA	4067
rs201738145	in-del	-/AAAAAAAGAG			intron-variant	LYN	GRCh38.p7	8:55906729	AAAAAGAAAAAGAAA[-/AAAAAAAGAG]AGAGAGAGGAGAGAG	4067
rs201807000	in-del	-/TTTTG	0.0162398	0.0886349	intron-variant	LYN	GRCh38.p7	8:55888734	GCACAATCCTTGGTT[-/TTTTG]TTTTGTTTTGTTTTG	4067
rs201818579	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55966382	AATTTTTTTTTTTTT[A/T]ATTGAGACGGAGTCG	4067
rs201831047	in-del	-/GT			intron-variant	LYN	GRCh38.p7	8:55953752	GACACTATAAGGCTA[-/GT]GTTCAACTTTTCTTT	4067
rs201842406	snp	A/C/G	0.000122584	0.00782814	intron-variant	LYN	GRCh38.p7	8:55966695	TTATAAAGCATGCCC[A/C/G]CCTTCTTTTTTCTTC	4067
rs201872970	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	LYN	GRCh38.p7	8:56011031	AAGAGTTTCCTTTGT[C/T]GCTTCAAATATTTGA	4067
rs201895605	snp	A/G	0.000115455	0.007597	missense	LYN	GRCh38.p7	8:55998374	TGGCATACATCGAGC[A/G]GAAGAACTACATTCA	4067
rs201934219	in-del	-/G	0.0240643	0.107019	intron-variant	LYN	GRCh38.p7	8:55940723	TGTAAGACAAGAACT[-/G]TGTCTGATTCAAATG	4067
rs201965711	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55986965	AAGTGATCCTTCCTG[C/T]TAGTCCTCACAAAGC	4067
rs201994602	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55891305	TGCAGTGAGTCGAGA[G/T]CCCGCGACTGCACTC	4067
rs202043164	in-del	-/AGATTTTGTAG			intron-variant	LYN	GRCh38.p7	8:55944433	CATACCATATGCTAT[-/AGATTTTGTAG]GTTTTAAAACACAAG	4067
rs202140152	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55968955	TTCTTAGGTAGGTTT[C/T]CACTTTTTTCCAAAG	4067
rs202164639	in-del	-/T			intron-variant	LYN	GRCh38.p7	8:56008129	GCCTCAAAAAAAAAA[-/T]AAAATAAAATAAAAT	4067
rs202195825	snp	A/C/T			intron-variant	LYN	GRCh38.p7	8:55887565	AAATATAAATATATA[A/C/T]ATATATATATACACA	4067
rs202196994	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55951432	ATGCTTTGGGAGGCC[A/G]AGACTGAGAATCACT	4067
rs202228069	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55909998	GTGTGTGTGTCTTTT[C/T]TTTTTTTTTTTTGAG	4067
rs207469198	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55916258	GAGGGGAAAGTGAAT[A/G]TTGAGAAAAAATAGT	4067
rs367574591	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55920794	CCCCACCACCCCCCC[A/C]CCGGGTTCCAGCAAT	4067
rs367581856	snp	A/G	0.000115949	0.00761321	intron-variant	LYN	GRCh38.p7	8:55947747	TCTCAAGCACGCCAC[A/G]GCTGCTCGTTTCCTC	4067
rs367600126	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55923792	TGATTTGCCTACCTC[A/G]GCCTCCCAATTGTTG	4067
rs367643862	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55916420	TCTGGACTTTGTCAG[G/T]TTACTTTGGGTGATT	4067
rs367644897	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55976912	AAACTAGGCCGAGCA[C/T]AGTGGCTCATGGCTG	4067
rs367652231	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55997786	GATTCTTCACACATT[A/G]GAAAATGTTAAGACA	4067
rs367661290	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55988373	TAAATGGTCTTTTTA[C/G]GTCAGTTTGGGATTG	4067
rs367829178	in-del	-/G	0.00398564	0.0444627	intron-variant	LYN	GRCh38.p7	8:55882307	AGCTTTCTTTTAGCA[-/G]AAAAGTGGTCCAGCA	4067
rs367840793	snp	C/T	1.76135e-05	0.00296757	intron-variant	LYN	GRCh38.p7	8:55966694	TTTATAAAGCATGCC[C/T]GCCTTCTTTTTTCTT	4067
rs367887258	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55934938	TCCCTTCTAGGGGGA[A/G]CCTGATGGCTCACCT	4067
rs367894940	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55934546	CACCGTGCAAGTGCA[C/T]GCAACTGGGAAACTT	4067
rs367903146	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55915762	TTACATATAAAACAT[A/T]TGAAGCAGTGCTGCC	4067
rs367963424	snp	A/G	0.00067518	0.0183612	synonymous-codon	LYN	GRCh38.p7	8:55969757	CGATGAAGGTGGCAA[A/G]GTGCTGCTTCCAAAG	4067
rs368010253	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55984043	CCATGTCTTGTTGAC[C/T]GCACTGCTCCTCTTC	4067
rs368029172	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55911291	TATATATATATTTTT[A/T]TTTTTTTTTTAGTAG	4067
rs368080471	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55883050	ACCTTAAACATGGTC[A/G]AAACACTCACATTAG	4067
rs368088890	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55973378	GACTACAGCAGCTTT[A/G]CCCACTGCTTTTCTC	4067
rs368134955	snp	A/G	0.00279162	0.0372561	intron-variant	LYN	GRCh38.p7	8:55929929	GGCCTGTTAGGAACT[A/G]GGCCACACAGCAGGA	4067
rs368202296	snp	C/T	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55963349	ATATGCCAGTCCCCA[C/T]GTCCCCTTTCCTGAC	4067
rs368220696	snp	A/C	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55957189	TGGACAAACTCCAAT[A/C]TTCAGTTGTTCAAAG	4067
rs368225390	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55977995	AGGACTTCTTCTGAG[C/G]TTTTTCAATTCAGAG	4067
rs368233871	snp	A/G			intron-variant	LYN	GRCh38.p7	8:56003217	GGTGCCCGCCACCAC[A/G]CCCAGCTAATTTTTT	4067
rs368238251	in-del	-/T	0.00358779	0.0422022	intron-variant	LYN	GRCh38.p7	8:55913863	GGGCACCAGAAGGTA[-/T]GAAGGGCCTTGGAGT	4067
rs368243934	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55983442	TTCACTTTCCCCTAC[A/G]TCCCTCTCCAGCTAC	4067
rs368244865	snp	A/C	0.00279162	0.0372561	intron-variant	LYN	GRCh38.p7	8:55903517	ACTTTTCATGAGCTG[A/C]ATAGTTTGAAAATTT	4067
rs368258680	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55890152	AAGAATAAATAAAAA[A/C]AAATAAAAATTACTC	4067
rs368277073	in-del	-/A	0.110153	0.210759	intron-variant	LYN	GRCh38.p7	8:55951246	GTGAGGCACTGTCTC[-/A]AAAAAAAAAAGAGAA	4067
rs368390395	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55978510	ACAGGCATTTTAGTA[C/T]AGGGGTCTGGGGCTA	4067
rs368390497	snp	C/G	0.000153988	0.00877328	missense	LYN	GRCh38.p7	8:55947620	TGTTCATCTTTAGAT[C/G]CAGAGGAACAAGGAG	4067
rs368403201	snp	A/G	0.0178098	0.0926698	intron-variant	LYN	GRCh38.p7	8:55911933	TGGGGTGTGGTGGGC[A/G]TCCAAATGGAGATGT	4067
rs368409310	snp	C/T	0.00279162	0.0372561	intron-variant	LYN	GRCh38.p7	8:55928451	ACGCAGGGCCCATTG[C/T]TGCTTTAATTTGCAA	4067
rs368432406	snp	A/G	0.00358779	0.0422022	intron-variant	LYN	GRCh38.p7	8:55948343	CCATGCATGATACTT[A/G]AAATGTCACTTTTCT	4067
rs368445189	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55974547	GAGTGAGAAAACAGT[A/G]TATAGATTGGGAAGC	4067
rs368474369	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55946414	TAAGAAAAGCTAAAC[A/C]GAATTTTTTTTTCTA	4067
rs368483911	snp	A/G	4.95152e-05	0.00497545	missense	LYN	GRCh38.p7	8:55950697	TGGTTTTTCAAGGAT[A/G]TAACCAGGAAGGACG	4067
rs368486816	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55968784	AAACTGTAATATAGC[C/T]TCTAGTACATGCCCA	4067
rs368497468	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55987570	TATGGGTGCCCGCCA[C/T]CACACCTAGCTAAGT	4067
rs368512301	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55906870	CCCTGTCCTTAATAA[C/T]CCTGTCCTATTGAGA	4067
rs368535046	snp	C/T			intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55922489	CCGAAGAATTATAAA[C/T]GTAGGCTGGGTGTGG	4067
rs368557371	in-del	-/T			intron-variant	LYN	GRCh38.p7	8:55899914	CAAAGTGCTAGGATT[-/T]ACAGGCATGAGCCAC	4067
rs368565301	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55909726	CCACCAATAGTGTAT[A/G]AGCATTGCCTTTTGT	4067
rs368619044	snp	G/T			upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55877947	AGATAAATATAAAAG[G/T]CAGTGCCTTCCCAAA	4067
rs368660358	in-del	-/ATGATATGAAAT			intron-variant	LYN	GRCh38.p7	8:55904347	AATATGATATGAAAT[-/ATGATATGAAAT]TCAACTTTACTAAAC	4067
rs368690462	in-del	-/AGG			intron-variant	LYN	GRCh38.p7	8:55906604	CAGGTAATCCACCTG[-/AGG]TCTCAGCCTCCCAAA	4067
rs368701760	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55954069	TTTCGATCAGCTTCT[A/G]AGCCAGACACTAAAT	4067
rs368716879	snp	A/G	0.0103094	0.0710523	intron-variant	LYN	GRCh38.p7	8:55947570	GAGGTTTGTTAAAAC[A/G]CTTCTGCTGATGGAT	4067
rs368723121	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55934259	CAAATCAGGTAAACA[C/T]AGCAAACAGAAGATA	4067
rs368755252	snp	A/G	0.00279162	0.0372561	intron-variant	LYN	GRCh38.p7	8:55942658	GGCACAGTGGCGGGC[A/G]CCTGTAATCCCAGCT	4067
rs368756281	snp	A/G	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55918266	GAGACAGACCACCCC[A/G]TTCCTCCCTCTCCTG	4067
rs368817685	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55938892	AGCTATGCTGTGCGC[A/G]AGTCTTTTAACCTTT	4067
rs368823941	in-del	-/TG			intron-variant	LYN	GRCh38.p7	8:55911097	ATATATATATATATA[-/TG]TACATACACGTATAT	4067
rs368839893	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55911199	TATATACACACACAC[A/G]TATATATATACACGT	4067
rs368871502	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55896004	TACATACCAGGTGCA[C/T]TTTCATTCTTCTCAA	4067
rs368881500	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55948381	TATTACTCATGTTTA[G/T]ACTGGGTTCATGGGC	4067
rs368928711	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55915322	TATTTATATTAACTA[C/T]AGTTTGTTTAAATAT	4067
rs368937087	snp	C/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55983463	CTCCAGCTACCTCAG[C/G]CTCCAGGTGTCTCCT	4067
rs368946104	snp	C/T	1.64849e-05	0.00287092	synonymous-codon	LYN	GRCh38.p7	8:55966782	TATGTCTGTGCAAGC[C/T]TTCCTGGAAGAAGCC	4067
rs368988380	in-del	-/TGAGT			intron-variant	LYN	GRCh38.p7	8:55910113	TCGGTTCATTCCTGT[-/TGAGT]ATTTCTTTTGCTGTG	4067
rs369005814	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55907858	GTGACAGAGTGAGAC[C/T]CTGTTTCACATAAAT	4067
rs369032064	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55999274	GCAGTGAGCCGAGAT[C/T]GCATCATTACATTCC	4067
rs369044484	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55887810	AGACAGGGCTTTGCT[A/G]TGTTGGCCAGGCTGG	4067
rs369059035	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55949650	TACGGATCAAGTCAG[C/T]GTAATTAGCATATCC	4067
rs369064704	snp	C/T	0.00279162	0.0372561	intron-variant	LYN	GRCh38.p7	8:55943557	CTCCAGCCTGGGTGA[C/T]AGAGCGAGACTCTGT	4067
rs369076388	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55996852	AGAGTGAATCTTGCC[A/G]GGCGTGGTGGCTCAT	4067
rs369098433	snp	A/C	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55903563	TTTCCCTTTAAGATC[A/C]GGGATAAATCATTTC	4067
rs369116010	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55904347	AATATGATATGAAAT[A/T]TGATATGAAATTCAA	4067
rs369128802	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55923675	CTCTTGAGTAGCTGG[A/G]ATTACAGGCGCCTGC	4067
rs369132174	snp	A/G	1.67576e-05	0.00289457	intron-variant	LYN	GRCh38.p7	8:55942041	CAAGATCAAAGCATG[A/G]CTACATAATTTAAAC	4067
rs369199289	in-del	-/AGAAA			intron-variant	LYN	GRCh38.p7	8:56003736	TAAAAAGGAAATAAA[-/AGAAA]GGAGGAAAAAGAAAA	4067
rs369227348	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55974604	CACCAGTATGTTGGT[C/T]GTAAATCAGGCTTGA	4067
rs369237375	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55975013	TACTGAGGCCTACAC[A/G]TTCCCAATCGCTCTT	4067
rs369245450	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55942391	TATGTGTATATATAT[A/G]TGTGTATATATGTGT	4067
rs369256669	in-del	-/ACACACACACACACACACACACACACAC			intron-variant	LYN	GRCh38.p7	8:55909011	TATATATATATATAT[-/ACACACACACACACACACACACACACAC]ACACACACACACACC	4067
rs369262330	snp	A/T			intron-variant	LYN	GRCh38.p7	8:56006208	TTTTCTGGCTGTTTC[A/T]GACCAGATATATCTA	4067
rs369294042	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55939641	GTGCGCTGTGGGTTG[A/G]CCGCACCCATGCAGG	4067
rs369302839	snp	C/T	0.000165145	0.00908543	intron-variant	LYN	GRCh38.p7	8:55953999	GGTAAGTGTGCGGCT[C/T]GGGGATCTATGTCCT	4067
rs369407141	in-del	A/TC			utr-variant-3-prime	LYN	GRCh38.p7	8:56010731	CTGCTCAGACCTGCT[A/TC]GACATGCCATAGGAG	4067
rs369422336	snp	C/T	0.00318978	0.0398085	intron-variant	LYN	GRCh38.p7	8:55985902	CCAGGCTCAGTGGCT[C/T]ATGTCTGTAATCCCA	4067
rs369442002	snp	A/C			intron-variant	LYN	GRCh38.p7	8:56004849	GAGTGCAGTAGCATG[A/C]TCATAGCTCACTGTA	4067
rs369470732	in-del	-/C	0.0154538	0.0865337	intron-variant	LYN	GRCh38.p7	8:55907129	CACAAAAAGACATGT[-/C]CAGTTCTATATATGG	4067
rs369478080	in-del	-/GTTT	0.00914312	0.0669923	intron-variant	LYN	GRCh38.p7	8:55886735	GCCAGCTCCATCAGA[-/GTTT]GTTTGTTCTGATGCA	4067
rs369484239	snp	A/G	1.66065e-05	0.00288149	synonymous-codon	LYN	GRCh38.p7	8:55950777	TAGAGAAAGTGAAAC[A/G]TTAAAAGGTAGGAAA	4067
rs369506756	snp	A/T			intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55923037	AACTGACAGGGCTTG[A/T]GGGAGGGTGGACCTA	4067
rs369511879	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55915208	CTAGAATGGATGCTG[C/T]CTGCCTTCCATATTC	4067
rs369513112	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55906709	AAGACCCAGTCTCTA[A/C]CAAAAAAAAGAAAAA	4067
rs369526470	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55884600	AGCTGTGATTACAGG[C/T]GCCCGCCACCATGCC	4067
rs369584937	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55979662	GCCTGGAATGCATTC[C/T]CCAGGTTTTGCTGAG	4067
rs369625638	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55935647	TGCTTGGTGGCGGAC[A/G]CCTGTAGTCCCCACT	4067
rs369641520	snp	C/T	0.000153988	0.00877328	intron-variant	LYN	GRCh38.p7	8:55950588	TTGTCATCTTGGTGG[C/T]TTTATTTGCCACATT	4067
rs369716594	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55906603	CTCAGGTAATCCACC[G/T]GTCTCAGCCTCCCAA	4067
rs369727459	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55903236	CACCTCAAGTGATTC[A/G]CCCACCTCAGCCTCC	4067
rs369730782	snp	A/T	0.0437281	0.141251	intron-variant	LYN	GRCh38.p7	8:55890134	AAAAAAAAAAAAAAA[A/T]AAAAGAATAAATAAA	4067
rs369732050	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55898941	GCAATCCTCCTGCCT[C/T]AGCCTCCTGTGTAGC	4067
rs369754051	snp	A/G	1.71076e-05	0.00292464	intron-variant	LYN	GRCh38.p7	8:55952152	AACAAGACAAGATAT[A/G]TTTGTTATGATATGT	4067
rs369845337	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55945064	CCTGGCCAGATATGA[C/T]AAAATGCACGCTATG	4067
rs369865013	snp	A/G			utr-variant-3-prime	LYN	GRCh38.p7	8:56010926	TTTTTCATTTCCACA[A/G]TTTCCTATATCCAGA	4067
rs369909483	snp	A/G	4.9579e-05	0.00497866	intron-variant	LYN	GRCh38.p7	8:55999574	ACTTAGCTATTTACA[A/G]TCAAGCTGTATAAAT	4067
rs369917988	snp	A/G	3.37952e-05	0.00411053	intron-variant	LYN	GRCh38.p7	8:55950416	ATACATGCATGGAGT[A/G]TGTAATCTTTTAGCT	4067
rs369931966	snp	A/G	6.59033e-05	0.00573997	synonymous-codon	LYN	GRCh38.p7	8:55999443	CCCTATTAAGTGGAC[A/G]GCTCCAGAAGCAATC	4067
rs369937559	snp	G/T	0.0189856	0.0955633	intron-variant	LYN	GRCh38.p7	8:55971009	CTGGGAAAACCCAAG[G/T]GAGGGCAATGCCCAT	4067
rs369957497	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55935312	GCAGCTTGGCCAGCC[C/T]GGGTTACCAGCTCAC	4067
rs369995572	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55906600	CACCTCAGGTAATCC[A/T]CCTGTCTCAGCCTCC	4067
rs370006995	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55992495	CAGCTCCATATGGAG[C/T]CTCCTCCTCCCTGCC	4067
rs370048780	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55942353	TATATGTGTATATAT[A/G]TGTGTATATATATGT	4067
rs370119023	in-del	-/TA			intron-variant	LYN	GRCh38.p7	8:55942357	GTGTATATATATGTG[-/TA]TATATATATGTGTAT	4067
rs370127952	snp	A/G	0.0023933	0.0345097	intron-variant	LYN	GRCh38.p7	8:55887398	TTTCAAACAATTTTT[A/G]TACTAAGATCTTAAT	4067
rs370155485	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55911962	GTGGAAGTTTGATTC[C/T]GAGTGAGCTCAATAT	4067
rs370172969	in-del	-/C			intron-variant	LYN	GRCh38.p7	8:55961037	TCTATGAAGAGACCC[-/C]TGAGGAAGGAAGGAA	4067
rs370238142	snp	A/G			intron-variant	LYN	GRCh38.p7	8:56001946	GCCAATGTGCACAAT[A/G]CCCAGGATTTGGAAA	4067
rs370280781	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55928296	GACTATAGGCAAGCG[C/T]CACCACGCCCGGCTA	4067
rs370286182	snp	A/C	1.65004e-05	0.00287227	intron-variant	LYN	GRCh38.p7	8:55950660	ACATAATATGCAGGA[A/C]ATGTTGAAATGTCTT	4067
rs370291126	snp	A/T	4.98484e-05	0.00499216	intron-variant	LYN	GRCh38.p7	8:55942004	CCAGTAAGTAGATAG[A/T]CTCAGGGGAGAATTC	4067
rs370297184	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55963012	ACGGGGATGGCCCCA[A/G]GCCATTCATGAGGGA	4067
rs370351987	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55911082	ATATATATATACATA[C/T]ATATATATATATATA	4067
rs370353205	snp	C/T			downstream-variant-500B	LYN	GRCh38.p7	8:56012464	CACAGTGGCTCATGC[C/T]TGTAATCTCAGCACT	4067
rs370367622	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55942526	GCGCGGTGGCTCACG[A/C]TTGTAATCCCAGCAC	4067
rs370389762	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55962461	ATTCATCTTCATCTC[A/C]TGTCGTGTTTGTGAG	4067
rs370424819	snp	A/G	0.00438332	0.0466095	intron-variant	LYN	GRCh38.p7	8:55997032	CAGGCATGGTGGTGC[A/G]TGCCTGTAATCCCAG	4067
rs370498424	snp	G/T	0.000121563	0.00779529	intron-variant	LYN	GRCh38.p7	8:56009875	TTTCTAAACGGCATG[G/T]GTTTCTGTTCTTTTT	4067
rs370527642	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55977099	CTTAGGCAGGAGAAT[C/T]GCTTGAACCCAGAAG	4067
rs370532472	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55940926	TGGCTTGCGGAGACC[A/G]TCATTTTGCTTTTAC	4067
rs370578313	in-del	-/G			intron-variant	LYN	GRCh38.p7	8:55975871	GAATCATGACTGGCT[-/G]GTTAAAATAGCAAAT	4067
rs370624542	snp	C/T	4.94988e-05	0.00497463	intron-variant	LYN	GRCh38.p7	8:55950638	TTCACCTTTTTCTTG[C/T]CGTGGAACATAATAT	4067
rs370636947	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55940184	CTTCCCCAAACTCCT[A/G]TCATCTCTCCTTCCT	4067
rs370653906	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55913879	GAAGGGCCTTGGAGT[A/T]CTGGGCTTTCTTATG	4067
rs370692743	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55915331	TAACTATAGTTTGTT[G/T]AAATATATTTTATTA	4067
rs370696932	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55886233	ATAGAACAGTGGCTG[G/T]CAAACATCTTTTTTT	4067
rs370707134	snp	A/G	0.00438332	0.0466095	intron-variant	LYN	GRCh38.p7	8:55909343	GTGGGGACAGTGGGG[A/G]CCAGCCATCCAGGGC	4067
rs370755577	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55887563	AAAAATATAAATATA[A/T]ATATATATATATACA	4067
rs370776571	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55950619	GGATTTCTTGTTAAT[A/G]TTCTTCACCTTTTTC	4067
rs370826842	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55955018	TCACACACATCTGAC[G/T]GGGTCACTTTTTCTG	4067
rs370837727	snp	A/G			intron-variant	LYN	GRCh38.p7	8:56000677	AGGTTGCAGTGAGCC[A/G]AGACTGCACCCCTGC	4067
rs370852365	in-del	-/ATAC			intron-variant	LYN	GRCh38.p7	8:55911167	TATATGTACATATAT[-/ATAC]ACGTATATATATATA	4067
rs370881506	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55911212	ACATATATATATACA[C/T]GTGTATATATATATA	4067
rs370914892	snp	A/G	0.00398564	0.0444627	intron-variant	LYN	GRCh38.p7	8:55939601	GCTCGGTCCGTGCTG[A/G]GAGGGAGCTGGATCG	4067
rs370920864	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55896529	GGCCTAAGGGAGAGA[C/T]GGCATTAGGAGAAAT	4067
rs370925398	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:56009460	AGACGTTTATTTTTC[C/T]GGGGTTCTGGAGTTT	4067
rs370939729	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55927997	AACTGCAAGACTGTC[G/T]TCCAGAATGGTTGGG	4067
rs371012195	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55901576	CAGGGCCTAGTGACA[A/G]GCAGAGGAATGTATT	4067
rs371054989	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55930675	GTGTGAAATTGCTCA[A/G]CTAAGAGTTATGCAA	4067
rs371062876	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55911184	ACACGTATATATATA[C/T]ATATACACACACACA	4067
rs371064707	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55972189	TCACTGGGAGAGTCA[C/T]GGGTCAGCAGCAGCC	4067
rs371131569	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55882454	ACAAAATTAAATCAT[A/G]TTATTCATGTACAAA	4067
rs371151751	snp	C/T	3.29538e-05	0.00405904	intron-variant	LYN	GRCh38.p7	8:55969699	GAATGCACTAACTTG[C/T]TCTTTCTTTCTCCAT	4067
rs371239899	snp	G/T			intron-variant	LYN	GRCh38.p7	8:56002581	CAGTCTAGCCTGAGC[G/T]ACAGGAAGGAGACTC	4067
rs371267504	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55984147	GCCCACCCTAAATCC[A/C]GGGTGAGATTTCATT	4067
rs371276691	snp	C/T	1.64776e-05	0.00287028	missense	LYN	GRCh38.p7	8:55952032	TTAAGCACTACAAAA[C/T]TAGAAGTCTGGATAA	4067
rs371329614	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55880740	GCCGAGGAGCAGTCC[A/G]GTGCTTTTGCCGGCT	4067
rs371353629	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55978766	GCAGGGAAACTGCCA[C/T]GGGACTTTGCGACAG	4067
rs371357449	in-del	-/AG			intron-variant	LYN	GRCh38.p7	8:55939463	CCTTTTCCCAAGAGA[-/AG]AGAGAGAGAGAGAGA	4067
rs371372546	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55988971	CGATAGTAATTAGGA[C/T]GAACAGAAGAGCACT	4067
rs371394281	snp	C/T	3.29516e-05	0.00405891	intron-variant	LYN	GRCh38.p7	8:55969814	ATATTCAAAAAGCCC[C/T]GTGTGCACGTGCATT	4067
rs371420064	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55935067	TAGCCTAGAGGTGAC[A/G]CCCACACCATGGAGG	4067
rs371462808	snp	A/G	0.000415162	0.0144017	intron-variant	LYN	GRCh38.p7	8:55947765	TGCTCGTTTCCTCAG[A/G]CCACTGAGTCCTGCA	4067
rs371487629	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55924988	CTGGGATTATAGACA[A/C]CCACCACCACACCTG	4067
rs371676612	snp	C/G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55965367	CTGCATCTCCTGGGT[C/G/T]GGGGAGGAGTGGAGG	4067
rs371690394	snp	A/G	0.00438332	0.0466095	intron-variant	LYN	GRCh38.p7	8:55969147	GCTGGGTGTGATGGC[A/G]TGTACCCTCAGCTAC	4067
rs371765768	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55942341	TATGTGTATATATAT[A/G]TGTGTATATATATGT	4067
rs371778212	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55904348	ATATGATATGAAATA[C/T]GATATGAAATTCAAC	4067
rs371877776	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55886778	TACATAGTTTCAGGG[C/T]ACATGTGATAATTTA	4067
rs371880836	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55990583	ATTTTAAGGTAAAAT[A/G]CTTTGATCTTCTTTA	4067
rs371884423	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55952540	ACTCCAGCCTGGGTG[A/T]CAGAGCAAGACTCTG	4067
rs371905058	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55947045	CTGTGGTCAGGAGTT[C/T]GAGACCAGCCTGGTC	4067
rs371939862	snp	A/G	3.3066e-05	0.00406595	intron-variant	LYN	GRCh38.p7	8:55999584	TTACAATCAAGCTGT[A/G]TAAATGAGAAAAAGT	4067
rs371950499	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55912620	TAATCCCAGCTACTC[A/T]GGAGGCTGAGGCAGG	4067
rs371957081	snp	C/T	1.64784e-05	0.00287035	synonymous-codon	LYN	GRCh38.p7	8:55952000	CAGAGACTTTGACCC[C/T]GTGCATGGTGATGTT	4067
rs371979527	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55978724	GGTTGCAGCGCAGGC[A/G]ACGGAGTTCTGACAC	4067
rs371992032	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55998324	CCTACATATGAAAAT[A/G]GGAGCCTATTTCTGT	4067
rs372001004	snp	G/T	0.0107246	0.0724382	intron-variant	LYN	GRCh38.p7	8:55963199	TCATTTTTGTGCTGA[G/T]GCAAGCATGCATGAG	4067
rs372078304	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55895683	TCAAATACCAGTCTT[A/G]GGACATTAGATGAAG	4067
rs372082564	snp	C/T	0.000115332	0.00759293	synonymous-codon	LYN	GRCh38.p7	8:55999515	TGGAATCCTCCTATA[C/T]GAAATTGTCACCTAT	4067
rs372096165	in-del	-/GGT			intron-variant	LYN	GRCh38.p7	8:55906605	AGGTAATCCACCTGT[-/GGT]CTCAGCCTCCCAAAG	4067
rs372100134	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55929089	TGCTCTTTTTGAAAG[A/T]TCAGTTGACTATATT	4067
rs372132706	in-del	-/T	0.00597247	0.0543191	intron-variant	LYN	GRCh38.p7	8:55897958	AAGATTAGTAAGCAA[-/T]TTTTTTCTTTGGAAA	4067
rs372144152	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55890142	AAAAAAAAAAAAGAA[A/T]AAATAAAAACAAATA	4067
rs372176194	in-del	-/TCT			intron-variant	LYN	GRCh38.p7	8:55985178	GGGAGGAACTGTACT[-/TCT]CTCACTGCTCTAAGT	4067
rs372245936	snp	C/T	0.0146672	0.084371	intron-variant	LYN	GRCh38.p7	8:55997900	CCATCCTGGCTAACA[C/T]GGTGAAACCCCGTCT	4067
rs372285574	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55935443	TGTTTAAATAAAGAC[G/T]GTCTGGCTAGGTCCT	4067
rs372291286	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55937792	CCTCTGCCTCCCAGG[C/T]TCAAGGGATTCTCCT	4067
rs372334895	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55906678	AAGAATTTGAGATCA[G/T]CTTGGGCAACGTAGC	4067
rs372348713	snp	A/G/T	0.000131797	0.0081168	synonymous-codon	LYN	GRCh38.p7	8:55947676	TGATGGCATCCACCC[A/G/T]GACGACTTGTCTTTC	4067
rs372420055	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55890156	ATAAATAAAAACAAA[A/T]AAAAATTACTCAGAG	4067
rs372438762	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55983554	CGCCCTCTCTTGAAC[C/T]TCCCACCCCTCGACC	4067
rs372477782	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55920328	TCCCATTCATAAAGC[C/G]TCTTTAGCAATTTTT	4067
rs372547745	in-del	-/ACAC/ACACACACACAC			intron-variant	LYN	GRCh38.p7	8:55887575	TATATATATATATAT[-/ACAC/ACACACACACAC]ACACACACACACACA	4067
rs372556778	in-del	-/CTAGATA	0.0107246	0.0724382	intron-variant	LYN	GRCh38.p7	8:55966251	AAAGAAAGAAAATTC[-/CTAGATA]CTTTTCATCTAGCCT	4067
rs372571904	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55926673	ATTGTAAAGACTATT[A/G]GGTGTTAAGAAGAAG	4067
rs372580201	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55965600	TCGCTCGTAATCACA[C/T]CATTGGAAATAACCA	4067
rs372591186	in-del	CC/T			intron-variant	LYN	GRCh38.p7	8:55936976	TTTATCCCTTTTCTA[CC/T]CCCCACGTCTTTTGT	4067
rs372595182	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55996570	TCTTACTTCCCTCCT[C/T]TCCTCCTCTCTCCTT	4067
rs372649948	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55903711	AACCTGGCTATTATT[C/G]TAAATGTAGAATTTA	4067
rs372663771	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55979926	TTGCTGCCTCCTGGC[C/G]TCTTCCCCTCCCCAC	4067
rs372667988	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55961279	TGTCACTCCACAAGA[C/T]GCTTTTTACTAGCTC	4067
rs372722695	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55951274	GAAAAGAAAAGAAAA[C/G]TACTGTAGAAAGCAC	4067
rs372741633	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55949381	CTTTAGTTGTAAGGC[G/T]GTTTTCCTTTGCTTC	4067
rs372750720	snp	A/C	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55922719	CTGCAGTGAGCTGAG[A/C]TTGTGCCACTGCACT	4067
rs372777006	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55889899	CTCAGCAGTTTGTTG[C/T]GAGTGTTCTAGGTTA	4067
rs372779356	snp	C/T	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:55901880	AAATGACTTTCAGAC[C/T]GTGATTTGGGTTAGT	4067
rs372823915	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55947229	ACTCCAGTCTGGGCG[A/T]CAAGAGCGAGACTCC	4067
rs372956584	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55982227	ACTACTTGCATGATT[A/C]TTAAAATTACATTTA	4067
rs372968573	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55938889	CCCAGCTATGCTGTG[C/T]GCGAGTCTTTTAACC	4067
rs372982802	snp	A/G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55996761	TTTCTATTCAGCAAC[A/G/T]AGTAGTAGTTTTGCC	4067
rs372990460	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55885050	CCAGTACCCCTTCTT[C/T]TGCTCTCCCCACTTC	4067
rs372996766	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55985925	TAATCCCAACATTTT[G/T]GGAGGCTGAGGCAGG	4067
rs373024775	snp	C/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55913888	TGGAGTACTGGGCTT[C/T]CTTATGGCTGCGAGA	4067
rs373081464	in-del	-/TG			intron-variant	LYN	GRCh38.p7	8:55914115	GTGTGTGTGTGTGTG[-/TG]CACGTATGACAGAGA	4067
rs373090603	in-del	C/TT			intron-variant	LYN	GRCh38.p7	8:55928901	CTAGGAGTTTTATAG[C/TT]TTTTGTTTTTCCTTT	4067
rs373098694	in-del	-/AC			intron-variant	LYN	GRCh38.p7	8:55911189	TATATATATATATAT[-/AC]ACACACACATATATA	4067
rs373111685	in-del	-/ATATAC			intron-variant	LYN	GRCh38.p7	8:55911102	TATATATATATACAT[-/ATATAC]ACACGTATATATACG	4067
rs373111858	snp	C/T	0.0023933	0.0345097	intron-variant	LYN	GRCh38.p7	8:55918919	AGCAGCGAGAATGGG[C/T]TGGGTGCAGTGGCTC	4067
rs373123784	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55979791	TCTAAGGCAGCTCCT[C/T]TCTGCCAAGCAGCAG	4067
rs373128303	snp	A/G	1.64836e-05	0.0028708	missense	LYN	GRCh38.p7	8:55966835	ATGACAAGCTCGTGA[A/G]GCTCTACGCTGTGGT	4067
rs373131704	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55997570	TCGTGAGGGCTCCAC[C/T]GTCCTGATCTAATCA	4067
rs373146349	snp	C/T			intron-variant	LYN	GRCh38.p7	8:56005447	CAGGTACTGTCCTGC[C/T]CTCGGCGCTGGCCTC	4067
rs373176523	in-del	-/AACA			intron-variant	LYN	GRCh38.p7	8:56006276	GTCCTGCTGCAAACA[-/AACA]CTCACCTTGGTCACA	4067
rs373176950	snp	C/T	1.65053e-05	0.0028727	synonymous-codon	LYN	GRCh38.p7	8:55953858	GGCTTGTGCAGAAGA[C/T]TGGAGAAGGCTTGTA	4067
rs373189388	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55942379	TATGTGTATATATAT[A/G]TGTATATATATATGT	4067
rs373238136	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55991576	CATTGTGTACAAGAT[A/G]CCAAGAGTTTCACCA	4067
rs373263234	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55902358	TTTGAGATGGAATTT[C/T]GCTCTGTAGCCCAGA	4067
rs373292999	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55906601	ACCTCAGGTAATCCA[C/G]CTGTCTCAGCCTCCC	4067
rs373294331	snp	A/C			intron-variant	LYN	GRCh38.p7	8:56004367	GGTGTGATATCGGCT[A/C]ACTGCAACCTCCACC	4067
rs373301912	snp	A/G	1.65397e-05	0.00287569	missense	LYN	GRCh38.p7	8:56009922	GGGAGAACTAATGCC[A/G]ACGTGATGACCGCCC	4067
rs373304146	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55991087	TAAGCAGCTGTGTCC[A/G]TAGTGGCCTCTGAGA	4067
rs373319149	in-del	-/C	0.0023933	0.0345097	intron-variant	LYN	GRCh38.p7	8:55981622	CTGCCTCCCAAAGTG[-/C]TGGGATTATAGGTGT	4067
rs373330325	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55944678	TAGAGATGGGGTTTT[G/T]CCATGTTGGCCAGGC	4067
rs373355731	snp	C/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55939710	GTGCTGCTATTAACG[C/T]ATTTGCCCATTTGTA	4067
rs373402665	snp	A/T	0.0437281	0.141251	intron-variant	LYN	GRCh38.p7	8:55890138	AAAAAAAAAAAAAAA[A/T]GAATAAATAAAAACA	4067
rs373423378	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55893094	GGGTTTGGCTACCAC[C/T]GGCATCTCTCTGTGT	4067
rs373427102	snp	A/G	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55908938	TTTTTTATGGCTGCA[A/G]AATACATAATTTTAT	4067
rs373428779	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55949806	TCCATCTACTTAAAG[C/T]GTACAATTCAGTGAT	4067
rs373437467	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55883650	CTGTAAACTTTGCCA[A/G]CCTCCTGGTTGTTTT	4067
rs373473378	snp	A/G			intron-variant	LYN	GRCh38.p7	8:56006257	AATTAGAATCAAGAA[A/G]TTTGTCCTGCTGCAA	4067
rs373481341	in-del	-/A			intron-variant	LYN	GRCh38.p7	8:55990239	TGAGACTCTGCCTCC[-/A]AAAAAAAAAAAAAAA	4067
rs373501493	snp	C/T			intron-variant	LYN	GRCh38.p7	8:56008744	ATGAGCACCTTACTT[C/T]TCTCCTGGAGGTCAG	4067
rs373570614	in-del	-/TATATATATATA			intron-variant	LYN	GRCh38.p7	8:55908990	ATTCCATTGTGTATG[-/TATATATATATA]TATATATATACACAC	4067
rs373582697	snp	C/T	0.000153988	0.00877328	intron-variant	LYN	GRCh38.p7	8:55950422	GCATGGAGTATGTAA[C/T]CTTTTAGCTTCTTTT	4067
rs373618459	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55935762	CTCCAGCCTGGGCAA[C/T]AGAGGGAGACTCCAT	4067
rs373625058	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55906719	CTCTACCAAAAAAAA[A/G]AAAAAGAAAAAAAAA	4067
rs373689283	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55887607	ACACACACACACATA[C/T]ATATATATTTTTTTT	4067
rs373739362	snp	C/T	0.00398564	0.0444627	intron-variant	LYN	GRCh38.p7	8:55942069	AACACCAGTCTGTAA[C/T]ATGTGCATGCAAAAA	4067
rs373796618	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55911112	ATACATACACGTATA[C/T]ATACGTATATATATA	4067
rs373848417	snp	A/T	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55923775	GAACTCCTGACCTCA[A/T]GTGATTTGCCTACCT	4067
rs373924067	snp	A/G	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55992243	GGTTTAGAACCAAAA[A/G]ATTTTATCGGTTTCC	4067
rs373934736	snp	G/T	0.00279162	0.0372561	intron-variant	LYN	GRCh38.p7	8:55957902	GCAGTGAGCTGAGAT[G/T]GCGCCGCTGTCACCA	4067
rs373938554	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55974868	GTTGCATTGAGATGT[C/T]GAGTCAGACGTGGTG	4067
rs373944750	snp	A/T	0.00597247	0.0543191	intron-variant	LYN	GRCh38.p7	8:55977196	GTCTCAAAAAAAAAA[A/T]AAAAATAAAAATAAA	4067
rs373950235	snp	C/G	0.000117957	0.00767885	intron-variant	LYN	GRCh38.p7	8:55950806	AATTGTTCAAAGCCT[C/G]TTTTAAAACACTATT	4067
rs373963923	in-del	-/A			intron-variant	LYN	GRCh38.p7	8:55997934	TAAAAATACAAAAAA[-/A]TTAGCCGGGCATGGT	4067
rs374033168	snp	C/T			intron-variant	LYN	GRCh38.p7	8:56009149	AAATTATTTTTTTCA[C/T]AAATATACTACAAGT	4067
rs374056232	snp	C/T	0.00517822	0.0506191	intron-variant	LYN	GRCh38.p7	8:55887717	CGGGTTCAAGTGATT[C/T]CTGTGCTTCAGCCTC	4067
rs374074483	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55997571	CGTGAGGGCTCCACC[A/G]TCCTGATCTAATCAC	4067
rs374077950	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55925078	TCCGCTTGCTTCAGC[C/T]TTCCAAAGTGTTGGG	4067
rs374086130	in-del	-/T			intron-variant	LYN	GRCh38.p7	8:55929593	AAACATCAGATTTCC[-/T]GGCATGAAGCTTTCA	4067
rs374087159	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55924642	GTGCTGAGATTACAC[A/G]CATGAGCCACCGCGC	4067
rs374104734	in-del	-/A	0.230017	0.2492	intron-variant	LYN	GRCh38.p7	8:55953753	CACTATAAGGCTAGT[-/A]GTTCAACTTTTCTTT	4067
rs374119811	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55935009	TCTGTGGTGGAGGTG[A/G]TGCCCACACCATGGA	4067
rs374127861	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55951296	AGAAAGCACACATGA[C/T]TGTGGCCAGTTCTTA	4067
rs374131736	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55958045	CGTCCTGCAGGGGGT[A/G]CCTGGCGAGGTTGGG	4067
rs374148288	snp	A/C			utr-variant-5-prime	LYN	GRCh38.p7	8:55877394	TGAGCCACTGAGCTC[A/C]GTCGCTTGGGGGCCA	4067
rs374209351	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55903486	TAAAAAACTACTTGA[A/G]TGTTTTTGATTACCA	4067
rs374212653	snp	C/T	0.000281096	0.011852	intron-variant	LYN	GRCh38.p7	8:55947569	TGAGGTTTGTTAAAA[C/T]GCTTCTGCTGATGGA	4067
rs374292382	snp	C/T	3.29495e-05	0.00405877	intron-variant	LYN	GRCh38.p7	8:55969714	TTCTTTCTTTCTCCA[C/T]AGGCAGTTTGCTGGA	4067
rs374300368	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55969033	CACCTATAATCCCAG[C/T]CCTTTTGGAGGCCAA	4067
rs374304320	snp	C/T	0.00676609	0.0577691	intron-variant	LYN	GRCh38.p7	8:56008050	CTTGAACCTGGGAGG[C/T]GGAGGTTGCAGTGAG	4067
rs374320915	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55893924	TGATCCTCCTGCCTC[A/T]GCTTCTCGAGTAGCT	4067
rs374324040	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	LYN	GRCh38.p7	8:55876762	GATGGGTTGCAGCAC[A/G]GATGATTTGGTGGAC	4067
rs374426902	multinucleotide-polymorphism	AG/TT			intron-variant	LYN	GRCh38.p7	8:55910171	TCTCATTTGTCTACT[AG/TT]TGTTTTTGTTGCCTG	4067
rs374524427	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55886026	TGCGAAGCCCACCCT[A/G]GCCATGCCTGACTTT	4067
rs374628647	snp	A/G			intron-variant	LYN	GRCh38.p7	8:56004032	CCTCCTTCTGAGTTC[A/G]AGCGATTCTCCTGCC	4067
rs374629151	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55902910	CTGGAGTGCAGCGGC[A/G]CAATCTCCACTCACT	4067
rs374633051	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55916509	AAAGCAGTGAAGACA[C/T]GTATCTACACCGAGG	4067
rs374634810	in-del	-/ATTTTA			intron-variant	LYN	GRCh38.p7	8:55908914	GCTGCAAAATACATA[-/ATTTTA]TTCTTTTTTATGGCT	4067
rs374656861	in-del	-/T	0.0310518	0.120672	intron-variant	LYN	GRCh38.p7	8:55980222	TATTGCAGTTGCTGC[-/T]TTTTTTTTTGTCTTT	4067
rs374667789	snp	C/T			intron-variant	LYN	GRCh38.p7	8:56003888	GAATTTCTGAAATTT[C/T]TAATTTTTTTACAAT	4067
rs374721362	snp	A/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55966219	TTGATTTTTGAATAA[A/T]TTAAACATTTTTTGG	4067
rs374740727	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55911186	ACGTATATATATATA[C/T]ATACACACACACATA	4067
rs374740951	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55897763	TAGGAAATTAAAAAA[A/C]TTAGCCAAGAGTGGT	4067
rs374742725	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55909970	ACTTTTTAATGGGGT[C/T]GTTTGTGTGTGTGTG	4067
rs374751924	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55883711	TAAATTAAGGAGACA[A/G]GGCTCATAGGACGCA	4067
rs374763747	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55991976	AACCTCACTGACATC[A/G]TCTCTTTACGTGATT	4067
rs374772696	snp	C/T	0.000347939	0.0131852	intron-variant	LYN	GRCh38.p7	8:55966663	GTGAGCCACCTCCCC[C/T]GGCTAGATTTTCTGT	4067
rs374876510	in-del	-/ATGA			intron-variant	LYN	GRCh38.p7	8:56001267	TGAATGAATGAATGA[-/ATGA]CGCACCTAGGCCATT	4067
rs374880395	snp	G/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:56009405	TATTAGTTGGCAAGG[G/T]CTGCCATAACAATAC	4067
rs374901357	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55882206	GCAAAGGTAGTTGGC[C/T]CAATCCAGAAGACCT	4067
rs374909038	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56004325	TTGAGACAGAGTCTC[A/G]CTCCGTCACCCAGGC	4067
rs374915252	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55981962	CTGCTTAATTTGGAG[A/G]GAAAAAACCCCACAA	4067
rs374928456	snp	A/C/G	1.64732e-05	0.0028699	missense	LYN	GRCh38.p7	8:55969752	AAGAGCGATGAAGGT[A/C/G]GCAAAGTGCTGCTTC	4067
rs374933722	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55987375	ATCAGGCACTACACT[C/G]CAGCTTGGGCTACAG	4067
rs374946440	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55940947	TTGCTTTTACCTGCG[C/T]TAGTACTCCTGGTTT	4067
rs375032150	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55901981	GTGAGTCAGTGATGA[C/T]GTATCATCATTCTAA	4067
rs375049226	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55915862	CGAGGATAAGAGAGA[A/C]CAAAGATGATGATTT	4067
rs375066799	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55964044	AGATCTACAGAAAAG[C/G]CCATATTGCTTGTAA	4067
rs375076996	in-del	-/TGAA			intron-variant	LYN	GRCh38.p7	8:56001245	TGATGGATGGATGGG[-/TGAA]TGAATGAATGAATGA	4067
rs375106422	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55911289	TATATATATATATTT[A/T]TTTTTTTTTTTTAGT	4067
rs375108210	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55942383	TGTATATATATGTGT[A/G]TATATATATGTGTAT	4067
rs375189802	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55890146	AAAAAAAAGAATAAA[A/T]AAAAACAAATAAAAA	4067
rs375193321	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55987153	CGCTGTGGCTCATGC[A/G]TGTAATTTCAGCACT	4067
rs375257874	in-del	-/C/CTTTC			intron-variant	LYN	GRCh38.p7	8:55902334	TTTCTTTCTTTCTTT[-/C/CTTTC]TTTTTTTTTTTGAGA	4067
rs375279721	snp	A/T			utr-variant-3-prime	LYN	GRCh38.p7	8:56010552	AGCATGACATTTCTT[A/T]GTGCTTTGGCTTACT	4067
rs375283590	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55961383	TTCAAACTACCAGAG[A/G]GTATCTTAGAAACCT	4067
rs375326905	in-del	-/C			intron-variant	LYN	GRCh38.p7	8:55888438	TAGTATGAAGCTAAT[-/C]TTTTTGTCCATCACA	4067
rs375342192	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55989684	TAACCAAACCAAAAA[C/T]CATCTGAGACAGGTC	4067
rs375370530	snp	C/T	0.00557542	0.0525036	intron-variant	LYN	GRCh38.p7	8:55999268	AAGGTTGCAGTGAGC[C/T]GAGATCGCATCATTA	4067
rs375394888	snp	A/C	1.6477e-05	0.00287024	synonymous-codon	LYN	GRCh38.p7	8:55950513	AAAAGAAGGCTTCAT[A/C]CCCAGCAACTATGTG	4067
rs375407677	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55902339	TTTCTTTCTTTTTTT[C/T]TTTTTTGAGATGGAA	4067
rs375437879	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55997860	GAGGCCAAGGCGGGC[A/G]GATCACGAGGTCAGG	4067
rs375466193	snp	C/G			intron-variant	LYN	GRCh38.p7	8:56004845	GCTGGAGTGCAGTAG[C/G]ATGATCATAGCTCAC	4067
rs375471610	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55905418	CCGTCTCAAAAAAAA[A/G]GAAAGAAAGAAAGAA	4067
rs375511334	snp	G/T	0.000119532	0.00772994	intron-variant	LYN	GRCh38.p7	8:55952151	CAACAAGACAAGATA[G/T]ATTTGTTATGATATG	4067
rs375530043	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55984649	GTAATCTAGGAGCTG[A/G]CTCTCTACTCCTGTG	4067
rs375540124	snp	A/T	0.000115499	0.00759844	intron-variant	LYN	GRCh38.p7	8:55951941	TGTGAGATATAAACA[A/T]TTACTTACACTTTTC	4067
rs375580772	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55911114	ACATACACGTATATA[C/T]ACGTATATATATACA	4067
rs375617127	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55965843	AAAATATTAGTCCTC[A/G]GCTGGGCACAGTGGC	4067
rs375628388	snp	A/C	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55936388	CTCATTCCTATAATC[A/C]CAGCACTTTGGGAGG	4067
rs375678561	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55885756	GGGGAAGCTGTGTCA[C/T]GGAGAGCAGAACTGT	4067
rs375705517	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55979917	CTGCCATAGTTGCTG[C/T]CTCCTGGCCTCTTCC	4067
rs375720243	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55891136	GGTGGGCGGATCACC[G/T]GAGGTCGGCAGTTTG	4067
rs375742628	snp	C/G	1.66596e-05	0.00288609	intron-variant	LYN	GRCh38.p7	8:55947773	TCCTCAGGCCACTGA[C/G]TCCTGCAGGCTGTCC	4067
rs375779367	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55952366	GAGTTCGAGACCAGC[C/T]TGGCCAACCTGGTGA	4067
rs375827920	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55940463	TCACTGCACCCTCCC[C/T]GGGCCGGGTTCAAGC	4067
rs375835961	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55984208	CTATTTCCAAATAAG[G/T]CCACATTCTGAGGTT	4067
rs375852644	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55996862	TTGCCGGGCGTGGTG[G/T]CTCATGCCTGTAATT	4067
rs375855491	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55957632	GTGAATTATTTCTTA[A/G]TAACACTGTTTTTAA	4067
rs375895931	snp	C/T	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55914119	GTGTGTGTGTGTGCA[C/T]GTATGACAGAGAGAG	4067
rs375931804	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55932910	GAATGGGAGCTAGGC[A/G]TTGAATACATATGGA	4067
rs375932752	in-del	-/GGGG			intron-variant	LYN	GRCh38.p7	8:55886231	GATAGAACAGTGGCT[-/GGGG]GTCAAACATCTTTTT	4067
rs375943358	in-del	-/G	0.5	0	intron-variant	LYN	GRCh38.p7	8:55967332	TTTTTTTTTTTTTTT[-/G]GAAACAGAGTCTCAC	4067
rs375952195	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55993050	TGATCCCTTAGGGGT[A/G]ATAAAAATCTTAGAT	4067
rs375974380	in-del	-/ATTT			intron-variant	LYN	GRCh38.p7	8:56004782	TGGCCACATACTTTT[-/ATTT]TTCATTTATTTATTT	4067
rs375990421	snp	A/G			intron-variant	LYN	GRCh38.p7	8:56006933	GCTTTCCTTGTACAT[A/G]AAAAGATAGGCTTCA	4067
rs376002964	snp	A/C	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55898817	ATAATAAATTTTAGG[A/C]AACTGGTTTTAATGA	4067
rs376003278	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55942345	TGTATATATATATGT[A/G]TATATATATGTGTAT	4067
rs376071735	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55996767	TTCAGCAACGAGTAG[C/T]AGTTTTGCCTCCCTA	4067
rs376215268	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55920716	CACTCTGTTGCCCAG[A/G]CTGGAGGGCAGTGGC	4067
rs376217002	snp	C/T	1.69335e-05	0.00290972	intron-variant	LYN	GRCh38.p7	8:56009890	GGTTTCTGTTCTTTT[C/T]GTTTTTTTCCACCCT	4067
rs376252093	snp	C/T	0.0383715	0.133092	intron-variant	LYN	GRCh38.p7	8:56002194	GGCCCACTTTGTGGG[C/T]GGATCACAAGGTCAG	4067
rs376260877	snp	A/G/T	0.00358779	0.0422022	intron-variant	LYN	GRCh38.p7	8:56003121	CTGGAGTGCAGTGGC[A/G/T]TGATCTCGGCTCACT	4067
rs376325157	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55993152	TCCTGTTAAGGATGC[C/G]TTAACTTTAAATTTT	4067
rs376326368	snp	A/C	0.00438332	0.0466095	intron-variant	LYN	GRCh38.p7	8:55997911	AACATGGTGAAACCC[A/C]GTCTCTACTAAAAAT	4067
rs376327592	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55981108	GCACTGAGCCCACCA[C/T]GCTCTTCCCTATCCC	4067
rs376329765	snp	A/G	1.64754e-05	0.00287009	missense	LYN	GRCh38.p7	8:55953957	GTGAAAAGGCTTGGC[A/G]CTGGGCAGTTTGGGG	4067
rs376345446	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55928779	TCATGGATCATTTTT[G/T]CTTTCATGGATCATT	4067
rs376391672	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55993630	AATGGAAGTAAAACC[C/T]ACCTGGTCAATTTGC	4067
rs376406888	in-del	-/TG			intron-variant	LYN	GRCh38.p7	8:55911156	ATACGTGTATATATA[-/TG]TACATATATATACAC	4067
rs376408911	snp	A/G	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:55894053	GTTCATCTTTCTGTG[A/G]GACCCACTAAGGGAC	4067
rs376416789	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55917067	CAGTAATCCCAGCTA[C/G]TCAGGAGGCTGAGGC	4067
rs376420521	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55904349	TATGATATGAAATAT[A/G]ATATGAAATTCAACT	4067
rs376432034	in-del	-/AAAT			intron-variant	LYN	GRCh38.p7	8:55966125	CAAGACGTAGTCTAA[-/AAAT]AAATAAATAAATAAA	4067
rs376472460	snp	C/T	0.000198518	0.0099609	intron-variant	LYN	GRCh38.p7	8:55954017	GGATCTATGTCCTTC[C/T]AGAGATGGTGACAGG	4067
rs376483435	snp	A/T	0.0437281	0.141251	intron-variant	LYN	GRCh38.p7	8:55890130	GACAAAAAAAAAAAA[A/T]AAAAAAAAGAATAAA	4067
rs376490650	snp	C/G	0.00517822	0.0506191	intron-variant	LYN	GRCh38.p7	8:55893836	TCACTATGTTGCCCA[C/G]GCTAGAGTGCACTGG	4067
rs376503308	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55917561	GAGTAGGGAAGGGGA[A/G]GATAGTGCTAATGAA	4067
rs376508272	snp	A/G	0.406641	0.194842	intron-variant	LYN	GRCh38.p7	8:55890139	AAAAAAAAAAAAAAA[A/G]AATAAATAAAAACAA	4067
rs376521113	snp	A/T	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55924068	TTCTTTTTCTTTCTT[A/T]TTTTTTTTTATTATA	4067
rs376527149	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55969847	CAAAGACTTCCCTGC[A/G]TCAAATTCATGAAGG	4067
rs376581101	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55920763	TGCAAGCTCCGCCCC[C/T]CCCCCCCTTGCCCTT	4067
rs376600895	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55906725	CAAAAAAAAGAAAAA[A/G]AAAAAAAAAAGAGAG	4067
rs376619976	snp	C/T	0.00318978	0.0398085	intron-variant	LYN	GRCh38.p7	8:55999315	ACAAGAGTGAAACTC[C/T]GCCTCAAAAAAAGAA	4067
rs376645658	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55935210	GTTAGGTTGCCTAAA[G/T]AAAAAAAACAAAAAC	4067
rs376768498	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55974480	CCTTTTTGAGTAGGA[G/T]GGCCTTTTAACAGCA	4067
rs376798929	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55938427	GATATAAAGTGCATT[A/T]TAAGCAAACTTGGAA	4067
rs376805196	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55913159	GATATATCCTGTGTT[C/T]GCTTCCTTTTCCCTG	4067
rs376842471	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55884374	CCTCACAAAATGCTG[A/G]GATTACAGGTGTGAG	4067
rs376859763	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55919952	CGTGACCCCACTCTT[C/T]GCTTCTTTGTCTGTC	4067
rs376872656	snp	G/T			downstream-variant-500B	LYN	GRCh38.p7	8:56012487	TCAGCACTTTGGGAG[G/T]CTAAGGCAGGAGGAT	4067
rs376913292	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55930598	AGTGTTCCCTTTTAT[C/T]GTTAAGAGAAACAAA	4067
rs376920695	snp	C/T	8.27369e-05	0.0064313	intron-variant	LYN	GRCh38.p7	8:55947741	AAGTGCTCTCAAGCA[C/T]GCCACGGCTGCTCGT	4067
rs376974174	in-del	-/A			intron-variant	LYN	GRCh38.p7	8:55952410	CTAGAAAAAAAAAAA[-/A]TTAGCCAGGCATAGT	4067
rs377001364	snp	G/T	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55995083	GGCAGGGCTCCTCTC[G/T]CCCAGCCGCCACCAA	4067
rs377089455	snp	A/G	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:55977117	TTGAACCCAGAAGGC[A/G]GAGATTGCAGTGAGC	4067
rs377099047	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55942285	TATATATACACACAC[A/T]TATATATGTGTGTGT	4067
rs377100066	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55964870	GTCATCTTTCTATGC[G/T]ATTCACATACAGATA	4067
rs377101074	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55903198	GGATTTCACCATGTT[A/G]GCCAGGCTGGTCTCG	4067
rs377104656	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55967357	TCTCACACTGTTGCC[C/T]GGGCTGGAGTGCAGT	4067
rs377129325	in-del	-/AGAAAGAAA			intron-variant	LYN	GRCh38.p7	8:55905418	CCGTCTCAAAAAAAA[-/AGAAAGAAA]GAAAGAAAGAAAGAA	4067
rs377130895	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55933119	ACCTAAAATAAAAGT[G/T]GAAATTATTTTTAAA	4067
rs377131019	in-del	-/CG			intron-variant	LYN	GRCh38.p7	8:55911682	CAGTCCTATGAGCTG[-/CG]GGGCACCTGCCCTGG	4067
rs377133663	snp	A/G			upstream-variant-2KB	LYN	GRCh38.p7	8:55876790	GACCAACATGAACAG[A/G]TGAGCAGCATGACCA	4067
rs377153434	snp	A/G	3.30929e-05	0.0040676	intron-variant, missense	LYN	GRCh38.p7	8:55941947	CGTAATACTGAAAGA[A/G]CTATTTATGTGAGAG	4067
rs377159566	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55887573	ATATATATATATATA[C/T]ATACACACACACACA	4067
rs377203010	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55947328	TATTTCCACATCTTG[A/G]CTATTTTGAATAATC	4067
rs377237219	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55914963	CTGGGGTTTCACCTG[C/T]TTTGAATTAGGGTAA	4067
rs377284208	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55978776	TGCCACGGGACTTTG[C/T]GACAGGGAAGTCTTT	4067
rs377287080	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55964080	CATTTAGATGTCAGA[A/G]CAATTTAATATATTC	4067
rs377309706	snp	A/C			intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55922765	AGAGCGAAATTCCAT[A/C]AAAAAAAAAAAAGAA	4067
rs377327132	snp	A/G	1.64836e-05	0.0028708	missense	LYN	GRCh38.p7	8:56009964	TACAGGATGCCCCGT[A/G]TGGAGAACTGCCCAG	4067
rs377330651	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55954811	CTGCACTCCAGCCTG[G/T]GTGACACAGTGAGAC	4067
rs377351884	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55906602	CCTCAGGTAATCCAC[A/C]TGTCTCAGCCTCCCA	4067
rs377361828	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55986133	GTGATCCTGCCACTG[C/T]TCTCTGTCCTGGGCA	4067
rs377378702	snp	A/C	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55914558	GCCCTGCCGGCCATC[A/C]ACATGCCTTCCAGGA	4067
rs377385978	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55885864	CATTTGCCTGCAGCC[C/T]CACCTTCCTTACCAC	4067
rs377386682	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55900164	AGTTCTGCCAACTTG[A/G]TGCAATTTTTACTAT	4067
rs377395077	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55967531	ATGTTGGCCAGGCTG[A/G]TCTCGAACTCCTGAG	4067
rs377411959	snp	C/T			intron-variant	LYN	GRCh38.p7	8:56004580	ATTACAGGCATGAGC[C/T]ACCGTGTGCAGCCAC	4067
rs377459791	snp	C/T			intron-variant	LYN	GRCh38.p7	8:56001917	CAGATCCATGTGCCT[C/T]CCAAGACCCCTCAGC	4067
rs377519602	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55950938	CAAACCTCAGTGATT[A/T]GTTGTGCTACTAAAA	4067
rs377562431	in-del	-/T	0.303438	0.244222	intron-variant	LYN	GRCh38.p7	8:56004294	TACAGAAAGACTTCC[-/T]TTTTTTTTTTTTTTT	4067
rs377581209	snp	G/T			utr-variant-3-prime, downstream-variant-500B	LYN	GRCh38.p7	8:56011894	ATTTCAGAACCACAA[G/T]TATTACCCAATATGT	4067
rs377589633	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55881026	TGGCTGTATATTTAG[C/G]GGACCGATTATTGAA	4067
rs377591853	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55887859	AAGTTATCCGGCTGC[A/C]TCAGCCTCCCGAAAT	4067
rs377595944	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55936144	TACTTTTAGGGACGA[A/G]TTCCTATAAATGATG	4067
rs377601406	in-del	-/T			intron-variant	LYN	GRCh38.p7	8:55902855	CATCTAGCATGAGGC[-/T]TTTTTTTTTTGGAGA	4067
rs377651953	in-del	-/A			intron-variant	LYN	GRCh38.p7	8:55886632	GGCAAAACAAAATAG[-/A]AAAAGGAAAATACAA	4067
rs377655428	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55944813	TGATGAATAAAGATG[C/T]CCTTTATTCAGAAAA	4067
rs377695215	snp	A/G			utr-variant-3-prime	LYN	GRCh38.p7	8:56012409	TGTGCAGCGGGAGAT[A/G]TATGTCAGTCTATTT	4067
rs377727290	in-del	-/TAAA			intron-variant	LYN	GRCh38.p7	8:55890156	ATAAATAAAAACAAA[-/TAAA]AATTACTCAGAGTGC	4067
rs377743551	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55986526	TAATGATTTAAATAT[A/G]GGTATTTGGTGAAGC	4067
rs386412818	in-del	-/TT			intron-variant	LYN	GRCh38.p7	8:55894376	ATTAACTTTCTTAAT[-/TT]TTTTTTTTTTTTGAG	4067
rs386412819	in-del	-/GTTT			intron-variant	LYN	GRCh38.p7	8:55932421	TATATTTTTTGTTTG[-/GTTT]TTTGTTTTTGTTTTT	4067
rs386725638	multinucleotide-polymorphism	CA/TG			intron-variant	LYN	GRCh38.p7	8:55886303	TGTAGTACAATGGTG[CA/TG]ATCTCCACTCACTGC	4067
rs386725639	multinucleotide-polymorphism	GA/TG			intron-variant	LYN	GRCh38.p7	8:55900082	AATGCGCTGCCACTC[GA/TG]ACTTCAGGAAGACAA	4067
rs386725640	multinucleotide-polymorphism	CA/TG			intron-variant	LYN	GRCh38.p7	8:55902250	CAACCTCAGGTGATC[CA/TG]CCCATTTTTGCCTCC	4067
rs386725641	in-del	-/AGAG/GA			intron-variant	LYN	GRCh38.p7	8:55906747	AAAAGAGAGAGAGAG[-/AGAG/GA]GAGAGAGAGAGAAAT	4067
rs386725642	multinucleotide-polymorphism	ATC/GTG			intron-variant	LYN	GRCh38.p7	8:55911484	TACTCAAGGAATTGC[ATC/GTG]AACCATCTCTTTTGT	4067
rs386725643	multinucleotide-polymorphism	AG/CC			intron-variant	LYN	GRCh38.p7	8:55926636	TTATTAAGACACAGC[AG/CC]GTAACGGCCTGCCCT	4067
rs386725644	multinucleotide-polymorphism	CTT/TTC			intron-variant	LYN	GRCh38.p7	8:55933708	CTGTCTCATTATCCT[CTT/TTC]TGCACTCCCTTCCAG	4067
rs386725645	in-del	AGT/CCTA			intron-variant	LYN	GRCh38.p7	8:55953751	GGACACTATAAGGCT[AGT/CCTA]GTTCAACTTTTCTTT	4067
rs386725646	multinucleotide-polymorphism	CA/TG			intron-variant	LYN	GRCh38.p7	8:55976628	CAAGGGCTGTCAGAG[CA/TG]GGCACCGCATGCTAC	4067
rs386725647	multinucleotide-polymorphism	CA/TG			intron-variant	LYN	GRCh38.p7	8:55994673	TGCTATTGTCAACTG[CA/TG]GTTTCAGGCCCAATT	4067
rs386725648	in-del	CACTTT/GAG			intron-variant	LYN	GRCh38.p7	8:56002183	GCACTTTGGGAGGCC[CACTTT/GAG]GTGGGCGGATCACAA	4067
rs397689986	in-del	-/C			intron-variant	LYN	GRCh38.p7	8:55933889	ATAACTAGATGACCC[-/C]TGGGTCTACCTACGG	4067
rs397714378	in-del	-/T			intron-variant	LYN	GRCh38.p7	8:55902025	CTTTCTTTTTTTTTT[-/T]GAGACGAGTTTCACT	4067
rs397787744	in-del	-/T	0	0	intron-variant	LYN	GRCh38.p7	8:55893808	GTTTTGTTTTTTTTT[-/T]AGAAGCAAGATCTCA	4067
rs397819302	in-del	-/A			intron-variant	LYN	GRCh38.p7	8:55904015	AGTCTCAAAAAAAAA[-/A]GTGTTTTATCATTTA	4067
rs397891417	in-del	-/A			intron-variant	LYN	GRCh38.p7	8:55942785	ACAAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA	4067
rs397892650	in-del	-/A	0.49533	0.0480965	intron-variant	LYN	GRCh38.p7	8:55976327	GCAAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA	4067
rs397936287	in-del	-/A			intron-variant	LYN	GRCh38.p7	8:55942803	AAAAAAAAAAAAAAA[-/A]GATGTAGTGAGATTA	4067
rs397954477	in-del	-/ATTT			intron-variant	LYN	GRCh38.p7	8:55908262	TTTATTTATTTATTT[-/ATTT]GAGACAGAGTCTCAC	4067
rs397960462	in-del	-/T			intron-variant	LYN	GRCh38.p7	8:55947991	ACAATTTTTTTTTTT[-/T]GAGATGGGATCTCTC	4067
rs398007909	in-del	-/T	0	0	intron-variant	LYN	GRCh38.p7	8:55902345	CTTTTTTTTTTTTTT[-/T]GAGATGGAATTTCGC	4067
rs398007910	in-del	-/GT	0	0	intron-variant	LYN	GRCh38.p7	8:55988329	TGTGTGTGTGTGTGT[-/GT]TTACATCCTATTTTT	4067
rs398095795	in-del	-/G			intron-variant	LYN	GRCh38.p7	8:55895458	TTTGGGGTGTCTGAG[-/G]AGCAGCATGATGTCG	4067
rs398095796	in-del	-/A			intron-variant	LYN	GRCh38.p7	8:55902613	GCATACAAAAAAAAA[-/A]CAACAACAACAGTAG	4067
rs398095797	in-del	-/C			intron-variant	LYN	GRCh38.p7	8:55968956	TCTTAGGTAGGTTTC[-/C]ACTTTTTTCCAAAGC	4067
rs527250014	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55935642	AGCCATGCTTGGTGG[C/T]GGACGCCTGTAGTCC	4067
rs527306125	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55980061	GCAGGCCACAGTCCC[C/T]GGGAGGTGGCCACAC	4067
rs527330460	snp	G/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55975916	TTTTGCTTTAAATTT[G/T]ATTGGGAAGCTTTGG	4067
rs527331362	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55897861	GAGGCTGCAGTGAGT[C/T]GAGATCGCGCCACTG	4067
rs527331473	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55891347	ACAAGAGCGAAACTC[C/T]GGCTCAAAAAAAAAA	4067
rs527343034	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55892065	GTCCTGGAGAAGGGT[C/T]CTTCTCCATCATTAA	4067
rs527348277	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55884927	ATTCCTTATTTGCCA[C/T]AGAGCTATTTCTTAA	4067
rs527399103	in-del	-/T	0.495927	0.0449436	intron-variant	LYN	GRCh38.p7	8:55893799	TGTTGTTTTGTTTTG[-/T]TTTTTTTTTAGAAGC	4067
rs527400132	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55885713	CAGAGAGGCTCTCTG[C/G]AGAGGGAGGACCACT	4067
rs527418955	snp	C/T	0.00835141	0.0640778	intron-variant	LYN	GRCh38.p7	8:55898371	TTGGCTCACTGCAAC[C/T]TCCGCCTTCCGTGTT	4067
rs527477967	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56009408	TAGTTGGCAAGGGCT[A/G]CCATAACAATACAAC	4067
rs527508795	snp	A/G	6.59239e-05	0.00574087	missense	LYN	GRCh38.p7	8:56010057	GACTACTTACAGAGC[A/G]TCCTGGATGATTTCT	4067
rs527565816	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55879239	GTACAGAAAGGTACA[C/T]GAGATAGGCATCCTC	4067
rs527647801	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55928740	TTTTAGATTTTAATG[A/G]AGTTCAATTTATAAT	4067
rs527718511	snp	C/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55969592	GGCTTTATATAACCA[C/T]ACAGAATTGCAAAGC	4067
rs527728297	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55884255	ACTTACAAGCATGTG[C/T]CACCACACCCAGCTA	4067
rs527759138	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55914066	GTGGACTAGCATGCA[A/G]CATGGAGAATGGAGA	4067
rs527766212	snp	A/G	0.00676609	0.0577691	upstream-variant-2KB	LYN	GRCh38.p7	8:55876904	TTTCCCACAGTGGAT[A/G]ATGGGATGCTCTTGT	4067
rs527791987	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55916747	CCTTTACCCCATGCC[C/T]AATACTGCAATGGCA	4067
rs527798610	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:56001115	GCAGGGACTCACAGA[A/G]GGAGGGAGTCTTGGG	4067
rs527832627	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56001840	GTGATGTGCTACCAT[A/G]GCCCCTGAGGCTTGG	4067
rs527833574	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55994861	CGCTCAATTGCTGCT[C/G]TCTCATCTGGGCTCC	4067
rs527855297	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55936539	CAGCTACCTGGGAGG[A/C]TGAGGCAGAAGAATT	4067
rs527924670	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55960006	TGGTTGCCTAGGGCT[C/G]GGGGGCCTGGGAGTA	4067
rs527950480	in-del	-/T			intron-variant	LYN	GRCh38.p7	8:55981772	CTGTACAAAACTTAC[-/T]TCATTGGTTGAAATA	4067
rs527974166	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55952514	GCAGTGAGCTGAGAT[C/T]GCGCCACTGCACTCC	4067
rs527994874	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55942653	AGCTGGGCACAGTGG[C/T]GGGCGCCTGTAATCC	4067
rs528021668	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55955432	TTCCACTCAGCAGAT[C/T]CATGGGTGTGAGTGC	4067
rs528075368	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55942654	GCTGGGCACAGTGGC[A/G]GGCGCCTGTAATCCC	4067
rs528084917	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	LYN	GRCh38.p7	8:56011598	GGCCAGATAGAATTT[A/G]TTTTCAAATAGGCTT	4067
rs528124026	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56004334	AGTCTCGCTCCGTCA[C/T]CCAGGCTAGAGTGCA	4067
rs528190392	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55998054	GCGCCACTGCACTCC[A/G]GCCTGGGTGAAAGAG	4067
rs528212161	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56005038	ATCCTCCCTCCTCAA[C/G]CTCCCAAAGTGCTGG	4067
rs528217436	snp	C/T			intron-variant	LYN	GRCh38.p7	8:56003262	GAGACAGGGTTTTGC[C/T]GTGTTAGCCAGAATG	4067
rs528228772	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55912237	TGCCCCTTTTGCAAT[C/G]TATCATTAAGGATGC	4067
rs528244519	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55998587	CAATTACAATAGTCA[A/C]CATTAAGAAAAACTT	4067
rs528286917	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55899931	CAGGCATGAGCCACC[A/G]TGCCCAGCCTTATCA	4067
rs528307131	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55905885	TGTTCCTGGGACACA[C/G]CTCTGGCAGTCCCAG	4067
rs528329054	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55992606	TATGATGGTAACAGT[C/T]TACCTGTGAGGTTGC	4067
rs528402516	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55898618	ATTGAGATATAATTC[A/G]CATATTGTATAATTC	4067
rs528408439	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55942458	GTATATATATATATA[C/T]ACACACATACATACA	4067
rs528427264	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55997327	ACTTTCTCCAACTCT[A/G]TTTTCATAGTTGGTT	4067
rs528467771	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55910861	GCTTTTTGTAGTTTT[C/T]GTATCAACACCTTGG	4067
rs528483743	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55904182	AATCTGAAATAAGTA[C/T]GATGAACAATTTTTT	4067
rs528514562	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55997880	ACGAGGTCAGGAGAT[C/G]GAGACCATCCTGGCT	4067
rs528535559	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55990806	CTAGTTTTTCAGGTT[C/T]CTTTGAAATCCCCTG	4067
rs528555475	snp	C/T	0.00279162	0.0372561	intron-variant	LYN	GRCh38.p7	8:55904663	GCTGAGGCAGGAGAA[C/T]TGCTTGAGCCCGGGA	4067
rs528569572	snp	A/T	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55983609	CCTCAGGACACTACA[A/T]CCAAAGGGCACCCAT	4067
rs528573764	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55991446	TTTCTTCTCATTGTA[C/T]GTTACAAAGGCCACT	4067
rs528576953	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55951332	CTTTGTTTGCTGAGC[A/C]TTTTGCATTATTATT	4067
rs528630323	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55937398	CAGCAATTCTTGATT[A/G]TTTGATTAAGAATGT	4067
rs528646515	in-del	-/A			intron-variant	LYN	GRCh38.p7	8:55881024	TCTGGCTGTATATTT[-/A]GGGGACCGATTATTG	4067
rs528681827	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55984265	CATTAGTTAATCCAG[C/T]ACAGCTGTCTAGACT	4067
rs528743686	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55932239	CTAAAAATGTAAGGA[A/G]AGGTAAAGCAAGAAG	4067
rs528753347	snp	A/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55887142	TTACTAATATGAAAA[A/T]TTTTTTTTCAAAAGC	4067
rs528784582	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55965236	AGTATTGCCCAGAGC[A/G]TGTTCCATGCGGTGT	4067
rs528814580	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55887775	CCACCATGCCCAGCT[A/C]CTTTTTGTATTTTTA	4067
rs528854370	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55987232	ACACTGGGGAACATG[A/G]TGAAACACCGTCTCT	4067
rs528877813	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55961210	CAAGCCAGTCACAGC[C/T]GGAATTAGAGTGCTC	4067
rs528896028	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55971948	GCTGTGGATTCCAGG[G/T]GGCTTCAGTTGACTC	4067
rs528901356	snp	C/G	0.000798403	0.0199641	upstream-variant-2KB, synonymous-codon	LYN	GRCh38.p7	8:55879473	CCTAATGTTGGAAGG[C/G]ATCAGAGCGCACCTC	4067
rs528905618	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55965137	AATTACTGAGAAAAG[C/G]CTTTCCCAAGAGAAA	4067
rs528909122	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	LYN	GRCh38.p7	8:56010808	CGCACAGCTGCCCTG[C/T]CTGCTCACCCGAAGG	4067
rs528913609	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55984740	ATAAATCAGATAACC[C/T]CCTCACTCTCAGCCC	4067
rs528972574	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55965954	ACATGGTGGAACCAC[A/G]TCTCTACTAAAAATA	4067
rs529033376	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55918269	ACAGACCACCCCATT[C/T]CTCCCTCTCCTGTTA	4067
rs529052677	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55997855	TTTGGGAGGCCAAGG[A/C]GGGCGGATCACGAGG	4067
rs529102713	snp	A/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55951573	GAGAGGTTGGGGTAG[A/T]AAGATCGTTTGAGCC	4067
rs529111640	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55958846	CATACATAACCTTTT[A/G]TTTATTCATCTATTG	4067
rs529131755	in-del	-/GAT			intron-variant	LYN	GRCh38.p7	8:55916580	CAGCCTGTGTTTGAC[-/GAT]GATCCCTGAGTGCCA	4067
rs529175955	snp	C/T	3.29908e-05	0.00406132	intron-variant	LYN	GRCh38.p7	8:55951954	CATTTACTTACACTT[C/T]TCCCCCCATAGGAAG	4067
rs529277240	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55960746	ATATTTTTGTTAAAC[A/T]TAAGGAATTGTTCAT	4067
rs529312887	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55964241	TTCTTTTTTTGTTTT[A/G]TTTTAGAGAAGGGGG	4067
rs529334950	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55950131	CTGCTGAGTAATACT[C/T]CACTGGATGGATATT	4067
rs529342454	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55996656	TCCATCCTTCCTTCC[C/T]TCCTTCCTTTCCTTT	4067
rs529349503	snp	A/C/G	0.000399281	0.0141238	missense	LYN	GRCh38.p7	8:55950781	GAAAGTGAAACATTA[A/C/G]AAGGTAGGAAATTGT	4067
rs529352036	snp	C/T	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55910744	CAATAAGGCTATAAG[C/T]TTAAGTCAAAAATTG	4067
rs529372992	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55903498	TGAGTGTTTTTGATT[A/G]CCAACTTTTCATGAG	4067
rs529408979	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55944431	CTCATACCATATGCT[A/G]TAGATTTTGTAGGTT	4067
rs529411971	snp	C/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55989699	CCATCTGAGACAGGT[C/G]TCCATCAATTTAGAG	4067
rs529428697	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55997118	AGTGAGCTGAGATCA[C/T]GCTACTGCACTCCAG	4067
rs529470060	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55990638	TTATACTAAAGTCTG[G/T]TTGGAATTTGGTATC	4067
rs529515825	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55892793	TGCAGGAGTGTGTGT[G/T]TATGTGTGTGTATGT	4067
rs529530034	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55942146	TAACTTTATCCTTTG[A/C]AGAATGTATAAATAT	4067
rs529537784	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55936748	AATGTATTGTATATT[C/G]CAAATAGCCGGAAGA	4067
rs529555643	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55984226	ACATTCTGAGGTTCC[A/G]GGTGGTCGTGAGTTT	4067
rs529569970	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55886300	GGCTGTAGTACAATG[A/G]TGCAATCTCCACTCA	4067
rs529596573	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55944262	AAAATTTAAAAACCT[A/G]TTACAGGCAGTGAAA	4067
rs529597931	snp	A/G	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55905360	AGATTGCAGTGAGCC[A/G]ATAGTGCCATTGCAC	4067
rs529599010	snp	C/T			upstream-variant-2KB	LYN	GRCh38.p7	8:55876980	TGAACACTGAATTAG[C/T]GAATACCGAGTCACT	4067
rs529608387	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55931117	ATATATAACTTGTAT[A/C]TGTTACTTTTTATAT	4067
rs529618995	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55919408	CTCTGTTAATATAGT[A/G]CTTTTCATAGAAATA	4067
rs529629738	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55893523	TATTTCAACTTCTGT[G/T]TCATGTAGTTTTGAT	4067
rs529630258	snp	C/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55937337	CAAAAACCGCAATTA[C/T]TTTTGCAACAGCCTA	4067
rs529638813	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55913591	CACATAAATTATTTT[A/G]TTAATGAAATGATTC	4067
rs529643209	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55999705	GGCTGGGCATGGTGG[C/T]TCACGCCTGTAATCC	4067
rs529671059	snp	A/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55915302	AAGCCTCTGCTATCC[A/T]GGTTTATTTATATTA	4067
rs529695357	snp	G/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:56000079	TGTGTGTTCTTGTTC[G/T]GCACTGATTAATTCC	4067
rs529723529	snp	C/T	0.00279162	0.0372561	intron-variant	LYN	GRCh38.p7	8:55953579	CTTGAACCCAGGAGG[C/T]GGAGGTTGCAGTGAG	4067
rs529725061	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55924453	CTGCAACCTCCATCT[C/T]CTGGGTTCAAGTAAT	4067
rs529725249	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55907495	GAAGGTGGTTACGTG[G/T]GCACATACATCTACC	4067
rs529743870	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55939944	GAACTGCAGCTCGCT[A/G]GTTTCAGAAAGAGGT	4067
rs529744118	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55948062	CACTGCAGCCTTGAA[C/T]TCCTAGGCTAAAGCA	4067
rs529752340	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55993293	TGGGAACCAGAACTT[C/G]GCCTGGGGAGAGCTT	4067
rs529764097	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55949628	TTTGATACATGTATG[C/G]AGTGTGTACGGATCA	4067
rs529857147	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55977311	AATGCTTATACTCAG[C/T]AAATAGTTTCAACAG	4067
rs529899900	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55981029	TCCCTGCTCAGCTCC[A/G]TTCAGTGGGTCCCCA	4067
rs529902430	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55987210	CTGAGATCAGGAGTT[A/C]GAGACCACACTGGGG	4067
rs529908680	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55969154	GTGATGGCATGTACC[A/C]TCAGCTACACAGGAG	4067
rs529955431	snp	C/T	0.00398564	0.0444627	intron-variant	LYN	GRCh38.p7	8:55997765	AATTTAGCAGGGTCT[C/T]GAAAAGATTCTTCAC	4067
rs529958462	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55896152	GCATGCCCCTGTCAT[C/T]CTAGCTGCTCTGGAG	4067
rs529986512	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55934627	GCATCTGGCTGTTTT[G/T]TCTTGACACCCCTTT	4067
rs529991244	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55935066	ATAGCCTAGAGGTGA[C/T]GCCCACACCATGGAG	4067
rs530016251	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55899799	GGATTGCAGGCACAC[A/G]CCACCATGCCCAGAT	4067
rs530030775	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55976800	AGTTGTAGGAACCTC[A/G]TGCATAAAGGCACAG	4067
rs530031399	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55985054	TGGGCTTCAATAGTC[C/G]GGAAACACTGCCATT	4067
rs530052848	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55928285	GGAGTAGCTGGGACT[A/G]TAGGCAAGCGCCACC	4067
rs530080946	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55946651	ATACATTTCAGCAGC[A/G]TTAGGTACATTCACA	4067
rs530091490	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55894946	CTTCAGCCTCCCAAA[A/G]TGCTGGGATTACAGG	4067
rs530094109	snp	C/G	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55887933	GATTTTAAAACGGCA[C/G]GATATAAGGAGCAAT	4067
rs530107289	snp	A/G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55985614	TCTTTAAGGTATTTT[A/G/T]TCTTAGTTGAAATAT	4067
rs530123474	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55933077	TTGCAACATACCCAT[A/G]TAACAAACCTGCACA	4067
rs530171881	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55979335	GCGTCAGCCACCGTG[C/T]CCAGCCTCATTCTTG	4067
rs530221200	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	LYN	GRCh38.p7	8:56012542	CAGCCTGAGCAATAT[A/G]GCAAGTCTCTACAAA	4067
rs530230236	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55888653	GCTTCAGCTTGTAAT[C/T]GTCATCTGCAAGTAG	4067
rs530312015	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55907469	TCAAGGAAGCTCTGT[C/G]TCTGGTTTTGGAAGG	4067
rs530323132	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55974429	GAAATTGGTAAAATG[A/G]GGAAGGTAGGAAAAC	4067
rs530357666	in-del	-/T			intron-variant	LYN	GRCh38.p7	8:55938347	TCTACGCATAAAATA[-/T]GTCTTTATTTACTGT	4067
rs530361186	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55920830	TGCCTCAGCCTCAGC[A/G]GGATTATAGGCATGT	4067
rs530363998	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55882357	GCCTTTTACTTCTAT[C/T]TGCAATATTTGTTTT	4067
rs530440962	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55960572	ATTGGTGATTTTATG[C/T]TACAAATAGACTGAA	4067
rs530489449	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55945129	GGTAGGGTTGATGCA[A/G]ATTCAACAACATTCT	4067
rs530490455	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55913479	CTAGAAAACACCAAC[C/T]TGAATAAAACGATTA	4067
rs530515317	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56005140	GCTGAAAGGTCCCCC[A/G]CTCTATTCCCAGCCA	4067
rs530518807	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55953040	TTGAGTCCCAAAACA[C/T]GGAGAGAGCAACGTG	4067
rs530519145	snp	A/C	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55920061	AATGCCAATTGAAAA[A/C]GACATCTGCAAACAT	4067
rs530519508	snp	G/T	0.00358779	0.0422022	intron-variant	LYN	GRCh38.p7	8:55960428	AGAAAATTTTGACTT[G/T]GGATCTTTTGCTTGT	4067
rs530524202	snp	A/G			intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55922245	GGCATGTGCCACCAC[A/G]CCCAGCTAATGTGTT	4067
rs530532276	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55946756	CCCCATTGCCTCCTC[C/T]CCCAGCCGCTGGCAA	4067
rs530552479	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56005593	TCCTCTTGGCTCAGA[C/T]CACTTCTTCCTCTGG	4067
rs530596313	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55968749	GTGCTTTGGATGCAA[C/T]CTTTGATTCCAACCC	4067
rs530643496	snp	C/G	0.000115539	0.00759975	intron-variant	LYN	GRCh38.p7	8:55999554	TCCCTACCCAGGTAT[C/G]GTTTACTTAGCTATT	4067
rs530647878	snp	C/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55967098	ATTGAAATCTAATCC[C/T]CCTGTTTTCTCTGCA	4067
rs530688953	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55993153	CCTGTTAAGGATGCC[G/T]TAACTTTAAATTTTA	4067
rs530700896	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55906643	ATTACAGGCGTGAGC[C/T]ATCACGCCTGGCCGA	4067
rs530700936	snp	A/G	0.00358779	0.0422022	intron-variant	LYN	GRCh38.p7	8:55900561	TTTTTTTTTTTTTTT[A/G]GTGGAGATAGGACCT	4067
rs530714108	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55915159	TATTTCAGTTTCCAT[A/C]GCTGTGTTGCAGCTG	4067
rs530717914	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55991743	ACACTCAGAGTTTTG[C/G]TCATGGTGCACCCCC	4067
rs530759967	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55940617	TTGACCTCGTGATCC[A/G]CCTTCCTTGGCTTCA	4067
rs530772341	snp	C/T	0.00318978	0.0398085	intron-variant	LYN	GRCh38.p7	8:55997952	AGCCGGGCATGGTGG[C/T]GGGTGCCTGTAGTCC	4067
rs530784265	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55945100	ATTAAAAGGGGAATT[G/T]GATGAGAAGGTGAGG	4067
rs530790984	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55904738	CTTGTAACAGAGCGA[A/G]ACTCCATCTCAAAAA	4067
rs530802722	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55972078	CCAGCCCGTGCCAGG[G/T]GAACTCATGTTCACA	4067
rs530803244	snp	C/T			intron-variant	LYN	GRCh38.p7	8:56000928	CATGGTATCTGCCCA[C/T]GTCCTTGAGAGTGAA	4067
rs530820601	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55939784	GGGAGGGTGACGGGG[A/C]GTGGGAGGGATGAGA	4067
rs530840780	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55950262	GTGGACATTATGGTT[G/T]CATCTTTCTTGGGTA	4067
rs530859851	snp	A/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55893747	AGAGTTAAAATGTTT[A/T]AAAAACTTTTTTTTA	4067
rs530865589	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55899623	GTGTGAAGTTGGTAC[A/C]GTTATCATCCCTTTT	4067
rs530865625	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55997898	GACCATCCTGGCTAA[C/T]ATGGTGAAACCCCGT	4067
rs530883208	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55949283	TAGCTATCCTGGGGC[A/C]AGTTACAAACCTTTT	4067
rs530900526	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55951896	ATCACAAAATGTGTA[C/T]TGCAGTTGTTGTATA	4067
rs530952954	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55937178	ACAAAATTTCTATAC[A/G]GGATCTTTTACCTCA	4067
rs530963709	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55932940	ATGTAAAGATAGGAG[A/C]AATAGACACGGGAGA	4067
rs531003159	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55984956	TTGGATTCTTGTTTA[A/G]AATCTGCAGGTGTCT	4067
rs531026831	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55933466	AGTTATTTTCTTATA[A/G]GTAATTTATTCCAAG	4067
rs531048018	snp	C/T	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:55894363	TGCCACTGTGCCAGA[C/T]TAACTTTCTTAATTT	4067
rs531073701	snp	G/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55888561	GGTGGAGAGTTGAAT[G/T]ACTCAAGGCTACTTC	4067
rs531080771	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55938285	AACAGACTAGAGTTG[C/T]ATTTGCATGTCAAAG	4067
rs531094589	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55905201	GGATCACCTGAGGTC[A/G]GGAGTTCAAGGCCAG	4067
rs531096197	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55884073	TTTAAAGACTTGGAC[C/T]TTTTGAGATTTTTGT	4067
rs531135520	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55919449	ATACGCTTCACTGCC[A/G]GGTCTGGAAACCCTC	4067
rs531138166	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55926579	AGTTTGGGAATTAAG[C/T]CAAGAAGATCTAATG	4067
rs531159958	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55887870	CTGCCTCAGCCTCCC[A/G]AAATCCGGGGATTAC	4067
rs531166776	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55995272	ACCACTGCCCACCTT[A/C]TGTTGACTTCCCATC	4067
rs531174273	snp	C/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55979187	AGCTGGGATTACAAA[C/T]GTGTGCCACCACGCC	4067
rs531180242	snp	A/G	0.00517822	0.0506191	intron-variant	LYN	GRCh38.p7	8:55902308	CCATTGCGCCTGGCC[A/G]TAACAGTGTACTTTC	4067
rs531188114	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55902413	GCTCACTGCAACTTC[C/T]GCCTCCCAGGTTCAA	4067
rs531188828	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55973174	GCCCTACTCTCCCCT[C/T]CGCATTCCCCTGTCA	4067
rs531218578	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55881551	GCCTGAATAAATTTC[A/G]CTGGATCATAGAGTC	4067
rs531231178	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55882254	TTGGTGTTACAAAGG[A/T]AGGTCGAAACTTTGT	4067
rs531258350	snp	C/T	0.000399281	0.0141238	synonymous-codon	LYN	GRCh38.p7	8:55966824	GACCCTGCAGCATGA[C/T]AAGCTCGTGAGGCTC	4067
rs531296763	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55988075	ATTTTGATCCCAAAA[A/G]AGTAGAGTACAAACA	4067
rs531300790	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55941637	TTAGAGCTGGATTTT[G/T]TCTGGGTGATGGAAA	4067
rs531322021	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55891308	AGTGAGTCGAGATCC[C/T]GCGACTGCACTCCAG	4067
rs531356500	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55929645	TTGAAGACATTTTTG[G/T]TTGTCACAACTGGTA	4067
rs531390794	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55890848	TCCTCCCACCTCAGC[C/T]TCTTGAGTAGCTGAG	4067
rs531413004	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55910071	GAAGGCATAGTTTGC[A/G]TATACTTTCTCCCAT	4067
rs531418252	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55923634	AACCTCCGCCTCCTG[A/G]GTTCAAGCGATTCTC	4067
rs531513072	snp	A/C	0.0023933	0.0345097	intron-variant	LYN	GRCh38.p7	8:55975752	GTTTCCTTCTGAAAA[A/C]GCCAAAGGAATAGGA	4067
rs531518083	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56009384	CAGAAATTTCCTTAG[C/T]TTCTATATTAGTTGG	4067
rs531524491	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55963555	GCTGCTCCAGAGTCC[C/T]TCCCAAGGGGCAGGT	4067
rs531528695	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55924124	AAATATATGCTGCTG[C/T]TGAAAGGAAGATAGC	4067
rs531546499	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55930069	AGGGATCTAAGTTAT[A/G]TGCTCCTTGTGAAAC	4067
rs531559516	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55934512	GCACTGCTGATTCGA[A/G]GGATGTTAAATGGAC	4067
rs531577052	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55976480	CTCTTGGTGTGGCCC[A/G]CTCCCTTTCACTCAC	4067
rs531578937	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55970198	ACTTTTAAGTCCTCT[C/G]TATTCTTGAAAACAG	4067
rs531590494	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55963075	TCCCCACCTCCAACA[C/T]TGGGGATCAAATTTC	4067
rs531620354	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55885636	TTTGGGTCTCTGGGT[A/G]CCCCCACTCTTCCTG	4067
rs531635925	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55890012	CTGGGTGAAGTGGCT[C/G]ATGCCTATAATCCCA	4067
rs531659873	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55915991	TCACAATTAATGGCA[C/T]CTTAATATTTTAAAG	4067
rs531678764	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55883723	ACAGGGCTCATAGGA[C/T]GCACATTAAAACACC	4067
rs531786391	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:56000403	TCTGACCATCCCTCC[A/G]TTTTTCCATGGTCTG	4067
rs531811112	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:56007453	AAAATTCTAGTCACA[C/T]AAATATTTGAAGATA	4067
rs531843687	in-del	-/CTT	0.0379877	0.132479	intron-variant	LYN	GRCh38.p7	8:56002185	ACTTTGGGAGGCCCA[-/CTT]TGTGGGCGGATCACA	4067
rs531845966	snp	C/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:56006825	GCCAACACCAACTAT[C/T]ACATGTAATCTTAGG	4067
rs531848080	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55961461	GATGAAAACCACCCT[A/T]TTGTTTCAATATCAC	4067
rs531849934	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55963904	CATGTAACTTAGGGT[C/T]AGAGTTAGGGCTGGG	4067
rs531868184	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55921621	TGCATAAATGGGTAG[A/G]AGTGCATGAGCCAAG	4067
rs531879639	snp	C/G	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55908471	GCTGGTCTCGAACTC[C/G]TAATCTCAGGTGATC	4067
rs531904665	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55994846	AGAGTCAGCTATGAC[C/T]GCTCAATTGCTGCTG	4067
rs531911139	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55988563	GCATAGGAAGACAAT[A/G]CATCCTTAGAGAGTA	4067
rs531922737	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55914347	GCACTTTATGTATTT[A/G]ACATGAAATATACTG	4067
rs531929696	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55922490	CGAAGAATTATAAAC[A/G]TAGGCTGGGTGTGGT	4067
rs531991433	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55908394	GGATTACAGGCACCC[C/T]CCACCGCGACCTGCT	4067
rs531995832	snp	C/T			intron-variant	LYN	GRCh38.p7	8:56007897	GCCGAGACAGGCAGA[C/T]GACTTCAGGTCAGGA	4067
rs532031914	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55955213	TGCTCACTTTCTCCT[G/T]TTGGCCCCTCTTGAG	4067
rs532052110	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55994738	CTTGGCCCAGTTTAT[A/G]TATAATTATTGGAAT	4067
rs532087303	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55994089	GTTTGAAATAGAGCT[A/G]GATTTACTTAGCCGT	4067
rs532090164	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55948844	ATGACAGTACCTAGA[A/T]CATGGGGTTGATGTG	4067
rs532104632	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55948163	AATTTTTGTAGAGAT[A/G]GGATCTTGTTATGTT	4067
rs532117549	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55934730	CCCTCCTGTGTTGAG[A/G]GGGGTGCACCCTGTA	4067
rs532129928	snp	C/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55935107	GATCTGAGGGATTCC[C/T]GGCACCGAAACAGCA	4067
rs532193233	snp	A/G	0	0	intron-variant	LYN	GRCh38.p7	8:55935512	GGTGCAGTGGCTCAC[A/G]CCTGTAATCCCAGCA	4067
rs532209016	snp	A/C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55896242	GCCACTGCACTCCAG[A/C/T]CTGGGTAGCAGAGCA	4067
rs532215515	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55981150	AGAGCCCACTTCCTG[A/G]AAGCGCTCACCCTTT	4067
rs532219676	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55928965	AATAGATGTAAGATC[C/T]GGGTCTAGATTATTT	4067
rs532245858	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55907562	CATTGTAGGTGCTTT[G/T]TTTTTGGTGGAAAAT	4067
rs532303396	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55929528	AGAAAGCATATTTTG[C/T]CCCAATCTGTAACAG	4067
rs532324939	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55970117	AGGCAGTTCCATGCT[A/G]TGTAAGCACAGCAGC	4067
rs532357523	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55986372	GATAATATCTATCTT[C/T]GGGGTAGTACAGTGA	4067
rs532379871	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55975200	ATGCTTGGAAACCTC[A/G]GCTTTCTCAGTATAC	4067
rs532384449	snp	A/G	0.00318978	0.0398085	intron-variant	LYN	GRCh38.p7	8:55901282	AAAACAGGAAAATTG[A/G]TAGAATTCCTCCACC	4067
rs532395309	snp	C/T	0.00279162	0.0372561	intron-variant	LYN	GRCh38.p7	8:55982153	CTTGTTCATTTTCCA[C/T]CCAGCGCCCCCAGTG	4067
rs532407732	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55891234	GTGCATGCCTGTAAT[C/G]CTGGCTACTTGGGAG	4067
rs532413675	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55884328	CAGGCTGGTCTTGAA[C/T]TCCTGACCCCAAGTG	4067
rs532417671	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55888721	AGATACAGTAATGGG[C/T]ACAATCCTTGGTTTT	4067
rs532418506	snp	A/G	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55926815	GTCTGTGCTGCCACA[A/G]TATACTTTTAAAAAA	4067
rs532419323	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55979896	CGGAAGACCCCACCC[A/G]AGCTCCTGCCATAGT	4067
rs532429263	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55889067	CTGTCGCCCAGGCTG[A/G]AGTGCAGTGGTGCTA	4067
rs532433152	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55954857	ATAAATAAATAAATA[A/G]ATAAATAAATAAATA	4067
rs532439891	snp	A/G	0.00478085	0.0486577	upstream-variant-2KB	LYN	GRCh38.p7	8:55877013	TTCTTAGGTTCCTGT[A/G]AGTCTCTGGACACAA	4067
rs532448888	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55949844	GTATAGTCACAGAAT[G/T]GTGCAATCATCACCA	4067
rs532450657	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55884747	GTGAGCCACCGTGCC[C/T]GGCCCTGTCTTGTAA	4067
rs532464499	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55979476	AACACAGCATTCTTC[A/G]CCTACCCTCGGAGCA	4067
rs532466821	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55922799	TGAATATGAAGTAAC[A/C]TGAAAATAGAATTCA	4067
rs532471418	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55933070	CAGCATCTTGCAACA[C/T]ACCCATGTAACAAAC	4067
rs532471807	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55956121	CTCATTAAAAAAAGA[A/C]TGACTTGGCTTCTTT	4067
rs532504926	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55933612	GGTGAGGCAATTACA[C/G]TCCAGAGAAAAGAGT	4067
rs532513604	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55971511	GGTTTGTCACACTTG[C/T]ACAGGGCTATGGAAC	4067
rs532554319	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55928038	TTCCCCAGCAATGAA[C/T]TGGAGTATCTGTTGC	4067
rs532558990	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56005824	CATGGTAGCTCATGC[C/T]TGTAATCCCAGCACT	4067
rs532589681	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55913676	TGAGTAGAATAGGAC[A/G]TGAGACAAGTGCTCT	4067
rs532617551	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55921379	GGGTTTACAGTCTAT[C/T]GAGGAGAGAGCTATA	4067
rs532630418	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55994105	GATTTACTTAGCCGT[A/C]GTAAATAGACCACCT	4067
rs532632926	snp	A/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	LYN	GRCh38.p7	8:55968359	CTCCCAGGTTCCAGT[A/G]ATTCTCCTGCCTCAG	4067
rs532684243	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55927392	TAATATGCATTTAAG[C/G]TTCCTCTATGTCCTT	4067
rs532696710	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55920873	GGCTAATTTTTGTAT[C/T]TTTAGTAGAGACAGG	4067
rs532700055	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55914202	CAGAGGGTTTTTAGG[A/G]TGGCCTGTGAGGTGT	4067
rs532702133	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55906953	TCCCTTGCAAAACAG[A/G]CTGACCAAATGCTGG	4067
rs532748791	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55983382	AAATTCCGCATTAGC[A/G]TTTTCCCTCACTTCT	4067
rs532760174	snp	A/G			utr-variant-3-prime	LYN	GRCh38.p7	8:56012347	ATTGTAGAGAACTGG[A/G]AAGACAGAATCCATA	4067
rs532766706	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55977116	CTTGAACCCAGAAGG[C/T]GGAGATTGCAGTGAG	4067
rs532785397	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55960638	TTAGTTTTCTCTTAC[C/T]CTTTTTAGTTTCTCA	4067
rs532790594	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55885784	TGTAGCCCGATGCTG[A/G]AGAGAAAAGGCCCCA	4067
rs532814590	snp	C/T			utr-variant-3-prime	LYN	GRCh38.p7	8:56010714	TTTTTCTTCTATGAA[C/T]ACTGCTCAGACCTGC	4067
rs532815449	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55984313	TCTAGCTCAGCCCAA[A/G]CTGCTCCCGTGAGCC	4067
rs532825037	in-del	-/TTTTTTTTTG			intron-variant	LYN	GRCh38.p7	8:55967323	TTTTTTTTTTTTTTT[-/TTTTTTTTTG]GAAACAGAGTCTCAC	4067
rs532846479	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55971198	GGAACAGAGGGGCAA[A/G]GAAAGGACCCAGCAG	4067
rs532849846	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55961448	CCTTTAACAGAGGGA[G/T]GAAAACCACCCTATT	4067
rs532892394	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	LYN	GRCh38.p7	8:56010218	GGGGATCATCTGCCG[C/T]GCCTGGATCCTGAAA	4067
rs532898898	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55936595	CAGTGAGCAGAGATC[A/G]CGCCATTGCACTCCA	4067
rs532906354	snp	A/G	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:55964342	GGATTACAGGCATGA[A/G]CCACCTTGTCTAGCC	4067
rs532910146	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55930192	GGACCACTGCTCTAG[C/T]TAACCTAGACTCCTG	4067
rs532926109	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55898338	CTGTCACCCAGGCTG[G/T]AGTGCAGTGGCACAC	4067
rs532974500	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55930935	GGATTAGAGATGTGA[A/G]CCCCCATGCATGGCT	4067
rs532975200	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55917588	TGAACTGTGACAGGG[C/G]CTAGCAAGAAAGAAA	4067
rs532992483	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55892753	CTAACAGGATTCGAG[A/G]GAATTTTTTAAAAAG	4067
rs532994021	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56003595	TCGCTTGAATGCTTG[A/G]ACCCAGGAGACAGAA	4067
rs532999958	snp	A/C/G	0.0023933	0.0345097	utr-variant-5-prime, synonymous-codon	LYN	GRCh38.p7	8:55880022	CCATACGCAGGTCCT[A/C/G]CTGGGCCGCCCCGTC	4067
rs533088126	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55924602	CTCCTGACCTCACGT[A/G]ATCCACCCCCCTTGG	4067
rs533092006	in-del	-/G	0.00993419	0.0697739	intron-variant	LYN	GRCh38.p7	8:55915888	GATTTCTGAAAAAAA[-/G]GAATGGATATTCAAT	4067
rs533158127	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55934910	TTCTCACTTCTCCTA[A/T]ATCATATCCTCCTCC	4067
rs533165181	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55923408	CATCCACTGCTTCCC[A/G]CTTCCAAAAATTTCT	4067
rs533186255	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55963009	ACCACGGGGATGGCC[C/T]CAAGCCATTCATGAG	4067
rs533210907	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime	LYN	GRCh38.p7	8:55877558	TCAAGATTTTTACTG[C/T]TCTGGGATGTGCATA	4067
rs533251073	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55956329	GAGATTAAGTGCAGA[C/T]GTGACTTGCTGAGTT	4067
rs533277137	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55951414	CTCAGGCCTGTAATC[C/G]CAATGCTTTGGGAGG	4067
rs533353539	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55915363	ACTCTTTAAAAAAAT[A/G]CTTCTGTGAAACCAG	4067
rs533393909	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56009131	ATAAGATAATATGTG[C/G]TAAAATTATTTTTTT	4067
rs533404120	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55989637	TAAATGAGTGCATTC[C/T]ACTCAAATGTTTCTA	4067
rs533414670	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55982839	TCCACTTCAGCCATT[C/G]CCTCCCTTCTGTCCA	4067
rs533424906	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55903493	CTACTTGAGTGTTTT[C/T]GATTACCAACTTTTC	4067
rs533466211	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55963427	AGTGGGTGGTTATCC[A/G]GAAGGAAGTGTGCAC	4067
rs533482791	snp	A/G	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:56002374	CAGTGAGCTGAGATC[A/G]CGCCACTGCAATCCA	4067
rs533486621	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55995587	GAGCAGGGAGCACTG[C/G]GGATGCATGCACACC	4067
rs533487867	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55933577	ATCCTCTCATGCCAA[G/T]CCCAGTGATTTCATT	4067
rs533523456	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55929045	TACCACTTATTGAAA[A/G]AAATATCCTTTCAGT	4067
rs533525825	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55989147	TCAGAGCCTGCGCCT[C/T]GGGTGGGAGAGAGCT	4067
rs533543074	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55903082	TCGAACTCCTGACTT[C/T]GCGATCCGCCCACTT	4067
rs533582841	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55884417	GCCTTTCTGGGGTAT[A/T]TTTGGCTTAAGTTAG	4067
rs533607912	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55941707	CAGGCAAACCTATTT[C/G]GGAACAGTATTCACT	4067
rs533619142	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	LYN	GRCh38.p7	8:55877233	CTTTAGCAAGCTCTA[C/T]GCTTCGGGCCATTTA	4067
rs533646483	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56008641	AGGATCAAAGATTGA[C/T]AGTTCAGCTTCTGAA	4067
rs533657551	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55990492	TTGGAAAGGGAATGG[G/T]ATTCTCTATAGAATA	4067
rs533686350	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55915681	ATTGCACTCCAGCCT[A/G]GGCGAGAAGAGCAAG	4067
rs533696208	snp	C/G	0.0023933	0.0345097	intron-variant	LYN	GRCh38.p7	8:56005352	CACTTTCCCCACCTC[C/G]ACTTGGGCCTAGCAT	4067
rs533741103	snp	C/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:56002156	GTGCAGTGGCTCACA[C/G]CTGTAATCCCAGCAC	4067
rs533774877	snp	C/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55995845	TTCTTTGTTTCCACT[C/G]GGAAGTGAAATACTG	4067
rs533780651	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55956488	TTTATTTAAAGTGAT[C/T]CAAAAGTTTAAATGG	4067
rs533781809	in-del	-/GCTC	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55972264	TACAACTAAGCACTG[-/GCTC]GCTCCATTTGAGTTC	4067
rs533871246	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55989661	GTTTCTAAAACTTTG[A/G]TCTCATTTAACCAAA	4067
rs533879088	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55903142	GTGAGCCACTGCGCC[C/T]GGCCTACGCCCAGCT	4067
rs533889747	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:56001395	CTTACTCTGCTGAGA[C/T]GCAAACCAGGGAAGG	4067
rs533907070	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55955646	TGTTTTTATCATCCC[A/G]AAAGGAAACAATGTA	4067
rs533931612	snp	A/G	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55923695	CAGGCGCCTGCTGCC[A/G]TACCCACCTGATTTT	4067
rs533938992	snp	A/C/G			intron-variant	LYN	GRCh38.p7	8:55958430	CTTGAGAAAATACAT[A/C/G]ACTTGAATAGATTTG	4067
rs533956409	snp	A/G			utr-variant-3-prime	LYN	GRCh38.p7	8:56011439	GTGTAAAAATTGGTC[A/G]TCAGCTGGGGGCGGG	4067
rs533971676	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55961650	TTTCCTTCGTCCTTT[A/G]CTCATACTTTTCTAT	4067
rs533981469	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55929108	GTTGACTATATTTGT[G/T]TGGTTCTATTTCTGG	4067
rs534017584	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55895777	ATCCAGTTGTTGCAA[A/G]GATTAAACGGGGTAA	4067
rs534032116	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55881571	ATCATAGAGTCTTTG[A/G]TGACTGGGCCTCTTT	4067
rs534054697	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55894679	CTATTATTACAGGCA[A/C]CTGCCACCATACCCA	4067
rs534101879	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55950367	GTAATATCTGTACAT[A/G]AATACATATTTATGG	4067
rs534162950	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55988184	GAATCAATGAATATT[A/G]ACAAGTAGAAAAGTG	4067
rs534177277	snp	A/C			intron-variant	LYN	GRCh38.p7	8:56008592	GAAAATGTTATTATT[A/C]TAATGATCTTTTTTA	4067
rs534190183	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55999839	AGCCAGGCATGGTGA[C/T]GCATGCCTGTAATCC	4067
rs534194505	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55890389	AATCATGATGAAATC[A/G]TGTCATGTTAAAAAA	4067
rs534232093	snp	A/G	1.72627e-05	0.00293786	intron-variant	LYN	GRCh38.p7	8:55953781	TTTATAGACACAGGT[A/G]AAGTACAAAGTATTG	4067
rs534295314	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55947823	CTACAGCCATAGCCC[A/G]GCCCCTTTCTTGTAA	4067
rs534315591	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55997620	CTAATACTATTGCCT[C/T]GGGGTTCAGGATTGC	4067
rs534346601	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55991065	CGGCAGTACTACCAC[A/G]TCAACTTAAGCAGCT	4067
rs534376236	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55939849	ATCAACTCTAAACCC[A/G]TGGCCATTTCAGAAA	4067
rs534400638	in-del	-/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55928843	GTATGTAAAATGTCA[-/T]CACCAAACCCAAGGT	4067
rs534453909	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55956465	ATCTACAGTAATCCA[C/G]CATCACTTTTATTTA	4067
rs534454872	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55898849	TTCCTTTTTTTAAAT[A/G]GACAGTTTCTTGCTC	4067
rs534490575	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55934884	TTTCCAACACTCCTT[C/T]AGACACCTCTTTCTC	4067
rs534517629	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55985115	TTTTCTAGGTCACGC[A/G]TCTTGCAAGGGAATG	4067
rs534535977	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55961488	TCACAGCCCTAAGAG[A/G]TCATCTGGGAGCTGC	4067
rs534557221	snp	C/T	0.408871	0.193029	intron-variant	LYN	GRCh38.p7	8:55911134	ATATATATACACATA[C/T]ATATATATACGTGTA	4067
rs534576589	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55969336	TTGCTGAATACAGAT[A/G]GGAGTGAGCCTGGCC	4067
rs534577332	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55894579	GTTCTGTTGCCCAGG[C/G]TGGAGTTCATTGGCG	4067
rs534591421	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56003864	GGTTATATTAATTTT[C/T]TTCTTGATGAATTTC	4067
rs534622851	snp	C/T	0.00279162	0.0372561	intron-variant	LYN	GRCh38.p7	8:55911625	ATATGTGAAATTCCA[C/T]TGTACTAGGGTGTCC	4067
rs534645356	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55997878	TCACGAGGTCAGGAG[A/T]TCGAGACCATCCTGG	4067
rs534654238	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55925616	CCACAGCCATGCGGG[G/T]ATGGGCGTTATTATT	4067
rs534667102	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55935814	CAGGAATTTGGGAAA[A/T]TTGATGCAAGACTGA	4067
rs534669143	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55943947	AATTAGCTGGGCATG[A/G]TGGCACATGCCTGTA	4067
rs534704207	snp	C/T			intron-variant	LYN	GRCh38.p7	8:56004169	ACTCCCGACCTCAGG[C/T]GATCTGCCTGCTTTG	4067
rs534705767	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55897464	AGCAGAAGATCTCCA[A/G]AGTCTAGTAACAGTT	4067
rs534724666	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55945397	CAACATAAAACTTCC[C/T]GACATAAACATTTGA	4067
rs534779961	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55937815	ATTCTCCTGCCTCAG[G/T]CTCCTGAGAAGCTGG	4067
rs534848821	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55930394	ACTATTATATGTATT[G/T]CTGAATATGGGTGGC	4067
rs534888564	snp	C/G	0.00438332	0.0466095	intron-variant	LYN	GRCh38.p7	8:55970843	TTCCATTTCAGAAGC[C/G]CTTTGCCTATTTGGG	4067
rs534893994	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55932621	AGACAGGGTTTCGCC[A/G]TGTTGGCCAGGCTGG	4067
rs534897792	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55938464	TTGGGGACACACATT[C/T]CCATCAGGAACCTGG	4067
rs534919017	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55989784	TGGGAACATGTGTCC[A/G]AGGTGGCTGGGATAC	4067
rs534947579	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55964594	ATACTTGGCTGGGCA[C/T]AGTGGCTCATGCCTA	4067
rs534958752	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55933152	AGAATTACTATACTC[C/T]TAAGCTATGAAAGCA	4067
rs534969123	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55989893	TCAACCCAGGAAGGC[A/G]GGATGTCTTGAAGCT	4067
rs535004764	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55957709	GCACTTCGGGAGGCC[A/G]AGGCAGGTAGATCAC	4067
rs535025234	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55983011	CTCCCCCATGTCACA[C/T]GCACCTGGTAAAATG	4067
rs535027247	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55891717	TTTATTTTACCACAA[C/G]TTTAAAGAATGAAAA	4067
rs535068747	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55966116	GGCGACAGAGCAAGA[C/T]GTAGTCTAAAAATAA	4067
rs535086721	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55965669	TGTTTATATGTGTGT[G/T]TCTGTGTATCTATAA	4067
rs535095167	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:56002843	GAGAGTTGTATGTTA[C/T]GAGAGCCTCTAGCAT	4067
rs535101200	in-del	-/TTGA			intron-variant	LYN	GRCh38.p7	8:55937400	GCAATTCTTGATTGT[-/TTGA]TTAAGAATGTCCAAA	4067
rs535106755	snp	A/C	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55996966	TCTCTACTAAAAATA[A/C]AAAAACTAGCATGGT	4067
rs535127886	snp	A/G	0.0023933	0.0345097	intron-variant	LYN	GRCh38.p7	8:55910455	AAAGATCAGTTGGCC[A/G]TAGATTTATAGCTTT	4067
rs535159242	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55958132	ACCCCCTGTTCTGTC[A/G]TAAGGTGTAAGTCTG	4067
rs535168029	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55932812	AAATCATGTCCTGGG[C/T]AGCAACATGGATGCA	4067
rs535215073	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56009665	GGCCTCATTTTAACT[C/T]AGTTACCTCTATAAA	4067
rs535221330	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55885900	GCTGCGTTTTCCTCG[G/T]GGTTCTTTCTACCCT	4067
rs535253172	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55980580	TTTGGCAAACAGAAG[A/C]AATTCAAGGTATACA	4067
rs535258480	snp	A/G			utr-variant-3-prime	LYN	GRCh38.p7	8:56010855	ACCTCCCAGGAAAGG[A/G]AGAAGAGCCTCAGAA	4067
rs535281668	snp	C/T	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55886329	CACTGCAACCCCTCC[C/T]CCCAGGTTCAAGCGA	4067
rs535291912	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, missense	LYN	GRCh38.p7	8:55879492	AGAGCGCACCTCCTC[C/T]GCTCCTGGGAGCACC	4067
rs535301687	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55983849	CTAAGTGATTCCATT[G/T]AAAGCATTGTATTAA	4067
rs535302719	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55991523	CCCATTAACTCAGGA[A/G]GCATTATTATTAATA	4067
rs535332708	snp	C/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55899300	ATAATAAATATTATG[C/G]TCACTTAACTACTAA	4067
rs535334942	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55893290	TGGTTTTTCTGCACA[A/G]CCAAGTCAATTTATA	4067
rs535376726	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55937070	TGCAAAGTCAGGCAA[C/T]AGACCCAGCAGTTGA	4067
rs535394524	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55931737	GTATTCTTTTGTGTT[A/G]AAGTATCATGTTCTA	4067
rs535400218	snp	A/T	0.00438332	0.0466095	intron-variant	LYN	GRCh38.p7	8:55917174	GAGTGAGATTCTGTC[A/T]AAAAAAAAAAAAAAA	4067
rs535408805	snp	C/T			intron-variant	LYN	GRCh38.p7	8:56008410	TGAGGAATGGAGCCC[C/T]TCTCATATGCCAGAT	4067
rs535460126	snp	A/G	0.0023933	0.0345097	intron-variant	LYN	GRCh38.p7	8:56003308	CCTTGGGATCCTCCC[A/G]CCTTGGCCTGCCAAA	4067
rs535472012	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55964486	GGTTGACTGCTAGCT[A/G]TAAATAAACTTTTTA	4067
rs535482061	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55949646	TGTGTACGGATCAAG[G/T]CAGCGTAATTAGCAT	4067
rs535484174	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55942321	TATGTGTATATATGT[A/C]TATATATGTGTATAT	4067
rs535509159	in-del	-/TTTTG	0.0159449	0.0878532	intron-variant	LYN	GRCh38.p7	8:55906336	AATTCGTTTTTTTTG[-/TTTTG]TTTTGTTTTGTTTTG	4067
rs535518057	snp	G/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55989185	AGCCGGTTTCACCGT[G/T]TGGGATGCTGGGGTT	4067
rs535588510	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55935728	AGAGGTTGCAGTGAG[C/G]CGAGATCGCACCACT	4067
rs535621661	in-del	-/TTAAT	0.0334286	0.124887	intron-variant	LYN	GRCh38.p7	8:56002627	TTAAATTAAATTAAA[-/TTAAT]TTAAATTAAATTAAA	4067
rs535640575	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55976169	AGTGGAGATGAAAGC[A/G]GTTTGAAATTAGCCA	4067
rs535656484	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55970432	AAGGAAATGCACACT[C/T]GAATGATGCCAGCTG	4067
rs535677149	in-del	-/GTGTGAT	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55887668	GGCTGGACTGTGATG[-/GTGTGAT]GTGTGATCTCGGCTC	4067
rs535702644	snp	C/T	0.0023933	0.0345097	intron-variant	LYN	GRCh38.p7	8:55885311	AGAAGTCTTCACAGC[C/T]CAGATAGTTTTTTAG	4067
rs535738283	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55945183	ATCTAGAGCAATAGT[A/G]TATGTGTGGCATACA	4067
rs535767050	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55984395	ATGCACCCCAACTCA[A/G]TGCCTATTACCCCCT	4067
rs535868502	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55985377	GAGAGCAGACGTCAC[A/G]GGCTTCCCTCGCAAA	4067
rs535872716	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55947025	GGCCAAGTTAGGTAG[A/G]TCACCTGTGGTCAGG	4067
rs535934694	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55882573	GTGATGCATGGATGA[C/G]TGTTAACATTGAAAG	4067
rs536032109	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55934158	TTGAACCCAGGAGGC[A/G]GAGGTTGCAGTGAGC	4067
rs536036621	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55982876	CTCCTGCAGCCGCTC[C/T]AGCCCCTACAGCCTC	4067
rs536057256	in-del	-/A			intron-variant	LYN	GRCh38.p7	8:55911870	GATGGAGAAGATGGG[-/A]AGGGGAGTGGGTTTC	4067
rs536091904	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55943449	GGTGTGGTGGTGCGT[G/T]CCTGTAGTCCCAGCT	4067
rs536104603	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55974109	ATAACGAGGTAAACT[C/T]GGACTTGGCCAAGGT	4067
rs536125014	snp	C/T	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55883291	AATAAATAGGTCATT[C/T]AACAAACATTTTAAA	4067
rs536132696	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55930238	TAGCTAATAAGCAGC[A/G]GAAGCTTATGGTGTG	4067
rs536143541	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55923819	GTTGGGATTAGAGGC[A/G]TGAGCCACCGCGCCC	4067
rs536226799	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55893833	ATCTCACTATGTTGC[C/T]CAGGCTAGAGTGCAC	4067
rs536262243	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55894719	TTTGTATTTTTAGTA[C/G]AGACGGGGTTTTGCC	4067
rs536264391	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55986054	AGCACCTGTGGTCCC[A/G]GTTACTCAGGAGGCT	4067
rs536332392	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55925315	TTCTTTTGTAGAGAC[A/G]AGTCTCATTATGTTG	4067
rs536349164	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56004158	GCTGATCTTGAACTC[C/T]CGACCTCAGGTGATC	4067
rs536355550	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55933874	CCCCTTCACATTGTG[G/T]ATAACTAGATGACCC	4067
rs536393564	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55926180	CTGAAGCCTCTCCCA[C/T]GTAGATTTACCCCCC	4067
rs536394214	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55947561	GTGCCCCATGAGGTT[G/T]GTTAAAACGCTTCTG	4067
rs536419036	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55927087	ATCACTGATAAGCCA[A/G]TGTTGATACATTAAT	4067
rs536428155	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55997977	TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG	4067
rs536429318	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55888930	GATTTTTGTCTTTCA[A/G]AACCACACTGGCTTT	4067
rs536431592	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55973615	ATAGACATGTCAAAC[C/T]GAGAGGAAAGAGCAG	4067
rs536434814	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55970489	CATTAGTAATGTTCA[A/G]CAGTTTGCTTGCTTG	4067
rs536468509	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55948863	GGGGTTGATGTGAGC[A/G]TGATGCATGTGTTTA	4067
rs536476083	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55882727	GCTCTGAAGTCTTCC[C/T]GAACTCTAATTTCAT	4067
rs536481259	snp	C/T			intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55922632	ATTAGCCGGGAGTGG[C/T]GGCACACGCCTGTAA	4067
rs536494931	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55889251	GAGACCAGGCTGTAA[C/T]CCCAGGCAGGAGTAC	4067
rs536532890	snp	A/T	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55920574	GGAAAATGAAGTTTA[A/T]TGAAGTAACTTGCTT	4067
rs536544953	snp	A/G	0.00795532	0.062565	intron-variant	LYN	GRCh38.p7	8:55973087	AGGGAAACTGTGAGG[A/G]GCAGAGTTGGGACTT	4067
rs536562218	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55953103	CCCTCCCATTCCTGT[G/T]TGCATCCGGCACATG	4067
rs536621220	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55932555	GCTCCTGAGTAGCTG[G/T]GATCACAAGCATGCA	4067
rs536630589	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55912347	CAGGCTTGAATACTC[C/T]TAGTCACAACCTTTA	4067
rs536649664	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55972149	CCCATAGTTCATCTG[A/G]CTCAAGTGCATGAAC	4067
rs536674514	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55945532	AGTACAAACTGTTTT[A/G]GTCCCATTCTGTGAA	4067
rs536693661	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55887355	GAAATAAAATATTCA[C/T]ATATGGACACATCAT	4067
rs536696449	snp	C/G			upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55878446	TGCCACACACGTTTA[C/G]TCAGGATCTCAAGGA	4067
rs536715036	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55920211	GAATTCCAGTAAAGT[A/G]AAGAGAGGGATAGAA	4067
rs536748616	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55946211	TGAGCACCTGGCACC[A/T]GCCCAGAACCTCGCT	4067
rs536752987	snp	A/G	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:55977673	ATCCCAGCTCTTTGG[A/G]AGGCTGAAGTGGGAG	4067
rs536817887	snp	C/T	0.00517822	0.0506191	intron-variant	LYN	GRCh38.p7	8:56000282	AAATAACCACCTTTG[C/T]TTATCAGTGGGAGGC	4067
rs536839672	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55979013	GAAAAAAATGTGATT[A/T]TTCTCTGTACTTAAA	4067
rs536852291	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55979524	TTTGTGTCTGTAGCT[C/T]TGCAGCTCGTGGGGC	4067
rs536873671	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55943082	TATTTGGTGTATTTC[A/G]GAAATACTTGGCAAA	4067
rs536878471	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55998165	TTTGGCAGAGGGTGG[C/T]CAGTTATTTTAGAAA	4067
rs536887871	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55895143	CAGTTTATTTCCTCC[A/G]GCCACAGTTCCTGAT	4067
rs536892925	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55959253	TTAGTGACCAAGCAT[A/C]TTTTCATGTCCTTCC	4067
rs536904426	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55952414	AAAAAAAAAAAATTA[A/G]CCAGGCATAGTGGTG	4067
rs536915830	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55973490	GAGCAGAGAGACTTT[A/G]CATAATTCCCTTGGC	4067
rs536959636	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55882617	TTAGTCAGGACATTG[A/T]TCAATGTCACATTGA	4067
rs537011831	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55930516	GCTTTGAATGTCCCC[C/T]TCTGGTCCTTTAAAT	4067
rs537049355	snp	A/G	0.00279162	0.0372561	intron-variant	LYN	GRCh38.p7	8:55905415	ACTCCGTCTCAAAAA[A/G]AAAGAAAGAAAGAAA	4067
rs537084304	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55992197	AATGAAGAGAATCAC[A/G]TGGCCTAAGATGAAG	4067
rs537115754	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55971432	ACACGGATCAATGAG[A/G]CCCTCTACTCAGGTG	4067
rs537124913	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55931596	TTTTTCTATTCATTT[A/G]TACCTTTTCCCTCAC	4067
rs537162563	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55938512	GCTGTGACTCATGAC[A/G]TCCCTGGCCCTTCTT	4067
rs537178823	snp	A/C	0.00279162	0.0372561	intron-variant	LYN	GRCh38.p7	8:55985343	TCCTTAGGTAAAGGA[A/C]AATGCAGGAGCAGCC	4067
rs537188126	snp	A/T	0.00279162	0.0372561	intron-variant	LYN	GRCh38.p7	8:55932410	AACAATTATATATAT[A/T]TTTTTTGTTTGTTTG	4067
rs537200594	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55925118	GTGAGCCACCGTGCC[C/T]GGCCTCTTTTTTTGT	4067
rs537227195	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55894624	TGCAACCTCTGCCTC[A/G]TGGGTTCAAGCTATT	4067
rs537227624	snp	C/T	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55964810	AGTCACTCCAAATTC[C/T]ACCAGCCAGGGATAA	4067
rs537263305	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55995145	TGCCCACTCTAGAAG[A/G]AGCTATCCTGAACTT	4067
rs537286545	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55957799	AATACAAAAAAAAAT[G/T]AGTTGAGCATGGTGG	4067
rs537300532	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55958402	TTTATTTAGACTGAA[A/G]CAGGATAAAAATCTT	4067
rs537319808	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55926386	TGCATGTATAGATGT[A/G]TAAGTTCAGAGCTAC	4067
rs537362563	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55951717	ATTTAAATGTAGCTA[A/C]ATAATAATTTTAAAA	4067
rs537427815	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55898627	TAATTCACATATTGT[A/G]TAATTCACTCAAAGT	4067
rs537432410	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55981245	CCATCCCAACTCCTG[C/T]TTACTCCATTCTCCT	4067
rs537433480	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55977018	GGTGAAACCCGGTCT[C/T]TACTAAAAATACAAA	4067
rs537445434	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55948412	CCAGCCTAGCTTGAG[G/T]TCTAAGGGTACTGAG	4067
rs537447973	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55977396	CTTTTTGTATTTACT[A/G]TAATATGTATTCATG	4067
rs537491991	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55893181	CGATTCAGTTGCTAA[A/G]ATTCTCACACATGAG	4067
rs537495082	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55886393	TACAGGCATGCACCA[A/G]TGCACCACCATGCCC	4067
rs537506649	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55970096	CACTTTCTCAGCATT[C/T]GGGAGAGGCAGTTCC	4067
rs537514455	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55883931	TGATACTTAAATTGT[A/G]AAACTTTAAGTTCAC	4067
rs537533597	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55928374	TGGTCTCCAACTCCT[A/G]ACCTCAGGTGATCCG	4067
rs537554060	snp	C/G	0.000798403	0.0199641	upstream-variant-2KB, synonymous-codon	LYN	GRCh38.p7	8:55879650	TGGCCCGGGCTGCTC[C/G]ACTCCCCGGAGCTGC	4067
rs537588235	snp	C/T	0.00438332	0.0466095	intron-variant	LYN	GRCh38.p7	8:55928902	TAGGAGTTTTATAGT[C/T]TTTTGTTTTTCCTTT	4067
rs537596686	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55922211	TCTCACCTCAGCCTC[A/C]TGAGTAGCTGGGCCT	4067
rs537638876	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime	LYN	GRCh38.p7	8:56010891	TCTGTGTTTAGAAGG[A/T]ATATTTTTAAGAGTC	4067
rs537665481	snp	A/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55918666	GGTTGTCTCGGTTAA[A/T]CCTTACTATGGCCTT	4067
rs537683143	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55962543	TCGTGTTGGTGAGAT[A/G]CATCTGTGGCTACGG	4067
rs537713654	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:56004005	TGGCGCCATCTCACC[C/T]CACTGCAACCTCCTC	4067
rs537752298	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56004445	ACTACAGGTGTGCAC[A/C]ACAATGCCCAGCTAA	4067
rs537770032	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55881604	ATGTAAATGTGTGGC[C/T]CTTTTGCTGAGTGAA	4067
rs537779387	snp	A/G	0.0115144	0.0749975	intron-variant	LYN	GRCh38.p7	8:55908987	GGTATTCCATTGTGT[A/G]TGTATATATATATAT	4067
rs537861547	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55974974	TAATCTCCCCTCCAC[A/G]TGGAAATTCTCATAC	4067
rs537904204	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55960745	AATATTTTTGTTAAA[A/C]ATAAGGAATTGTTCA	4067
rs537904399	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55969112	ATGGTGAAATCCTAT[C/T]TCTACAAAAAAAAGA	4067
rs537908513	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55975240	CACAGCTGGTGGTTA[A/G]CTCTTTCTCAGAATT	4067
rs537940641	snp	C/T			intron-variant	LYN	GRCh38.p7	8:56006980	TTCTTCTTATCAAGT[C/T]GAATTCCCCAAACAG	4067
rs537942318	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55892266	TCTCTTCTAAAAATC[C/T]AAAAATAGCCAGGTG	4067
rs537949842	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56007158	TGCAAATGAGGGATC[C/T]CCAGGAAGGAAGTGA	4067
rs537956105	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55884396	AGGTGTGAGCCACTG[C/T]GCCTGGCCTTTCTGG	4067
rs537959154	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55999778	GGAGTTGGAGACCAG[A/G]CTGACCAACATGGAG	4067
rs537979979	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55913747	TTTGTCTGGGGATTC[A/G]GCACAGTTTTTATGG	4067
rs538005151	snp	A/G	0.0023933	0.0345097	intron-variant	LYN	GRCh38.p7	8:55914648	CCAGATAACAGAATG[A/G]CCATAGTGGTGATTA	4067
rs538018793	snp	C/T	1.64757e-05	0.00287012	intron-variant	LYN	GRCh38.p7	8:55969711	TTGTTCTTTCTTTCT[C/T]CATAGGCAGTTTGCT	4067
rs538054183	in-del	-/AC	0.00318978	0.0398085	intron-variant	LYN	GRCh38.p7	8:55883191	ATGGGTACTTGAAGT[-/AC]AGTTTTTATTGAATG	4067
rs538084644	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55994140	CAACAACAAATTAAG[A/G]TTTTAAAAAAAATAA	4067
rs538106211	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55927398	GCATTTAAGGTTCCT[C/T]TATGTCCTTTCATGG	4067
rs538115510	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55895801	GGGGTAATGTACCTG[G/T]GAGTTCCTTGAAGAG	4067
rs538132975	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55906018	ATTCAGTAGTTTTGT[A/G]TTGTTGCTTTTCTTT	4067
rs538147479	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56002095	AGACCAGCCTGGCCA[A/G]CATGGCAAAACCCCA	4067
rs538153917	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55948695	AAGGACAAGGTGTTC[C/T]GTGGTTGAGAGCAAT	4067
rs538156958	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55956414	GGAGGCATAGTATTA[C/G]CCGGTCCTATTCTTA	4067
rs538157344	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55941020	CATCTGAATGTTTTC[A/G]TAAGTATCTTCTCTC	4067
rs538209825	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55913885	CCTTGGAGTACTGGG[A/C]TTTCTTATGGCTGCG	4067
rs538212479	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55933891	TAACTAGATGACCCT[C/G]GGTCTACCTACGGCT	4067
rs538237182	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55995462	GCCTCTGTCCCACTT[C/T]TCAAGTCCCTCATGA	4067
rs538252343	snp	A/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55913049	TGGGATGTCTGCCTG[A/T]TGAAACCATTTTACT	4067
rs538253793	snp	C/G	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55901523	GGAACTACTTCTGGT[C/G]GTTTCCCTGGACTTA	4067
rs538258626	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55921026	GTAAAAGATTTTCAG[C/G]CCACATTCTTTGAAT	4067
rs538266101	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55895743	AAAACAGTAATAACA[A/G]ATTTTTGTTTGGTAT	4067
rs538305897	in-del	-/T			intron-variant	LYN	GRCh38.p7	8:55902494	ACAACGCCCAGCTAA[-/T]TTTTTTTTTTCTAGA	4067
rs538336496	snp	A/C/G/T	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55939534	TGCAGGAACGCAGTG[A/C/G/T]GGGGGGGACAGGGGA	4067
rs538388100	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55927723	GCCTGTAATGCCCAG[A/C]TACTCAGGAGACTGA	4067
rs538395553	in-del	-/ACA			intron-variant	LYN	GRCh38.p7	8:55909049	CACACACACACACAC[-/ACA]CCCCACATTTTCTTT	4067
rs538400357	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55928303	GGCAAGCGCCACCAC[A/G]CCCGGCTAGTTTTTG	4067
rs538401363	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55886622	CATATCTGTAGGCAA[A/C]ACAAAATAGAAAAAG	4067
rs538440026	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55974910	CCGCAGGTGATTGAC[A/G]TGGTTTGCGGTTTAA	4067
rs538447770	snp	A/C	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:55986876	GACCACAAGCATGTG[A/C]CACTACACCCGGCTA	4067
rs538467028	snp	A/G	1.64874e-05	0.00287113	synonymous-codon	LYN	GRCh38.p7	8:55947712	AGGAGAGAAGATGAA[A/G]GTCCTGGAGGAGTAA	4067
rs538506175	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55961770	AGCAGACAGAAAATG[C/T]AAACACAAATATCTA	4067
rs538518886	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55940264	TTACACATCACATGG[A/G]GAGCAGCATGCTCCC	4067
rs538520086	snp	C/T			intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55923103	TGAGGGTTTGAGCCT[C/T]GGGTGACTGGAATGG	4067
rs538570146	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55954763	TCACTTAAGCCAAGG[A/T]GGTCGAGGCTGCAGT	4067
rs538627209	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55895386	ATCTTGGTGAATAAT[A/G]TAGGTATGGATTAGT	4067
rs538632910	snp	C/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55979713	CCCAGCACAGCTCTG[C/T]AGATCTCACCCTGAT	4067
rs538645293	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55980336	AGTTTTGAGCTGCTC[C/T]GCTTCTGACCTGGGC	4067
rs538646482	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55880794	AGAATTCAGGGGTTG[C/T]CTTTCCTTCGCCTTG	4067
rs538651081	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55888959	TTTTGTATTATTTCA[A/G]ATTTGATAGATGCCC	4067
rs538698145	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55974364	GATGGAGGTTATGCT[C/T]AAGGTATATTTTACC	4067
rs538712909	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55929881	TAGATCAGGCATCCC[A/C]AACCCCTGGGCCATG	4067
rs538719042	snp	A/G	0.00478085	0.0486577	downstream-variant-500B	LYN	GRCh38.p7	8:56012647	TTGCTTGAGCCCAGG[A/G]AGTCAAGGCTGCAGT	4067
rs538719050	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56004631	ATTCCCCATGCCTGC[A/G]GGTGCTCCTCAAAGT	4067
rs538756359	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56005243	CAGTTTTGCCCTAAT[G/T]TCTGGTTTATTTCAC	4067
rs538764112	snp	C/T	0.000722756	0.0189962	intron-variant	LYN	GRCh38.p7	8:55998305	GCACTTTCCAGTCAC[C/T]TACCCTACATATGAA	4067
rs538781691	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55921110	TACGTCTGAAACGAA[A/G]ACAATTTTGGGAGTT	4067
rs538786458	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55920398	TTCTTAAGTGTGATC[A/G]TGTCACTATAACCTG	4067
rs538810463	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	LYN	GRCh38.p7	8:55967863	AAACATACTAATAAA[C/T]TGCCAAATTATTTTT	4067
rs538838272	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55912966	ATATTTTGTATTATC[A/G]ATATTTAACCACTAG	4067
rs538854031	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55914021	GGAAACAGGGGAGAG[A/G]TGAAATCATGGCTGC	4067
rs538899366	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55948029	TCCAGGCTAGAATGC[A/T]GTGGCATGATCATAG	4067
rs538905501	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56007009	AGGGTGGAGCATGTC[C/T]AGCCTTTACCAGCAT	4067
rs538923723	snp	A/G	0.0150606	0.0854603	intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55922755	CTGGGCAAAAAGAGC[A/G]AAATTCCATCAAAAA	4067
rs538924182	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55924653	ACACGCATGAGCCAC[C/G]GCGCCCAGCTGCATC	4067
rs538943618	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56000614	GCATCTGTAATCCCA[C/T]CTACTTGGGAGGCTG	4067
rs538979282	snp	C/T	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:55926330	GATTGAGAGCAATGG[C/T]TCTGCAGGATTAGTA	4067
rs538981857	snp	A/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55993439	CAGAAGCATTTAGTT[A/T]TGAGTACTGAGCTCT	4067
rs538983590	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55890290	ACACTCCATCCTGGG[C/T]GACAGAGCGACAGCC	4067
rs539028043	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56008697	AAAAACATTCTCTAT[C/T]ACCAGGCCTTTTGCA	4067
rs539038716	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55919724	CCTTCCCTTCTCAGC[A/G]GGAGGCCAGCTGGGG	4067
rs539050626	snp	A/C	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55881863	TGTCCAAAATGATAG[A/C]CCCAGTGCCTGGTAC	4067
rs539055531	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55956580	CTGTGGGAAGTTTAA[C/G]ATTATGTAAATAGAA	4067
rs539068196	in-del	-/T			intron-variant	LYN	GRCh38.p7	8:55895628	ACCTCATCTCTACAA[-/T]TTTTTTTTTTAAAGG	4067
rs539072725	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55877904	TTTAAAGCACCCAAC[A/G]TAATTTCTGGGAGGT	4067
rs539079982	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55916175	AAAAAATTTTTATTG[A/G]GATGATCATTGGCTA	4067
rs539097146	snp	A/G	0.0023933	0.0345097	intron-variant	LYN	GRCh38.p7	8:55959309	GAAACGTATGTTCAA[A/G]TCCCTTTCTCACTTT	4067
rs539115287	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56009463	CGTTTATTTTTCCGG[G/T]GTTCTGGAGTTTCAA	4067
rs539116941	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55980280	CAGGCTGGAGTGCAG[C/T]GGCTTTTCACAGGCA	4067
rs539154447	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:56002738	CACCAGAATCCATCG[A/G]CTAGTCTGTTCCCTG	4067
rs539209040	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55948533	TGCTGACTCAGACAT[C/G]TGGCAGTGTCAGACC	4067
rs539237033	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55903204	CACCATGTTGGCCAG[A/G]CTGGTCTCGAACTCC	4067
rs539252763	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55992913	ATCACCTCCTAAAGG[C/G]CCCCCCTCTTAATAC	4067
rs539261498	snp	A/T			intron-variant	LYN	GRCh38.p7	8:56008358	GGTATAATCTACAGC[A/T]TTGAAAAAGAGATAG	4067
rs539311538	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55904259	TCTTTATGGCTATAG[G/T]GTAACCAAATTCAGG	4067
rs539316708	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55947034	AGGTAGATCACCTGT[A/G]GTCAGGAGTTCGAGA	4067
rs539351883	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55944028	CGGGAGGGAGAGGTT[G/T]CAGTGAGCCGAGATC	4067
rs539353319	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55975166	GTGATGGTCCCTGAG[C/T]GGGCATTGCTTGGAG	4067
rs539376153	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55891972	GGAGAGGGAATGATA[A/G]TGGAGAAATTTACAA	4067
rs539417842	snp	C/T	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55923206	AAAAATTTTTTGAAA[C/T]GAATTGGGGGTGGCC	4067
rs539480568	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55994919	AGGCATCGTGGTTCT[A/G]TCGCCAAAAGCCTAC	4067
rs539528062	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55995999	ATGTGAAAACCCCAG[C/T]CCATTTCCCAAAGGA	4067
rs539548908	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55949114	CGAGCATGGTGCTGA[A/G]GCTCACTTGCTTGGA	4067
rs539560793	snp	A/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55942083	ATATGTGCATGCAAA[A/T]AAATTCCATTGATTA	4067
rs539569016	snp	C/T	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55988516	TAGGGCTTTTGAACA[C/T]CATTAATTATGTGAA	4067
rs539609245	snp	A/T	0.00398564	0.0444627	upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55879131	TGGTTAGGCACCAGC[A/T]GCTACGTGCAAGCAC	4067
rs539621904	snp	A/G	0.00478085	0.0486577	intron-variant	LYN	GRCh38.p7	8:55896839	TGCCTTCCGGGTTCA[A/G]GCAATTCTCCCTACC	4067
rs539637153	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55978393	GGGGCAGCTGAGGAC[C/T]GCCATTGCGGGCACG	4067
rs539651061	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55975510	TGCAACTAATGATTC[G/T]GAGGCTATGCAGATG	4067
rs539651132	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55982451	TTGTCAATGGAACCA[A/G]TGGTGTGCTGAGGTA	4067
rs539680643	snp	G/T	3.35076e-05	0.004093	intron-variant	LYN	GRCh38.p7	8:55950443	AGCTTCTTTTTGATG[G/T]GTATTTCTATTCTAG	4067
rs539718392	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55884497	AGTTCGCTCTTGTCA[A/C]CCAGGCTGGAGTGCT	4067
rs539732758	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55944546	AGTGCAATGGCACCA[A/T]CTCAGCTCACTGCAA	4067
rs539741153	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55990891	TTTACATGTTTTAAA[A/C]CTCATACCCTGGGGA	4067
rs539755077	snp	A/T	0.00318978	0.0398085	upstream-variant-2KB	LYN	GRCh38.p7	8:55877268	TATTTTTATTTTTTT[A/T]AATTTTTTTATTGTG	4067
rs539772577	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55983119	CTAGCAGCTTTCTGC[A/G]TTTCCAGTTCAAGAG	4067
rs539780582	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55929339	GACTAAGAATACAGT[C/T]GGGATGATGCTTTTC	4067
rs539799812	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55982939	CTGCCTGTCCCTACC[A/G]CCCCTCCGCTCCTGC	4067
rs539812874	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55914143	GAGAGAGAAAGAAGA[C/G]GGAATATGAATGGCA	4067
rs539820732	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56007226	TATTTATATCATACT[G/T]GATGTTAGTCCTCCC	4067
rs539832480	snp	G/T	0.00318978	0.0398085	intron-variant	LYN	GRCh38.p7	8:55908180	AAAATAGAATTAAAG[G/T]TGATAAGGGCATCAA	4067
rs539844359	snp	G/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55908917	GCAAAATACATAATT[G/T]TATTCTTTTTTATGG	4067
rs539855680	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55948538	ACTCAGACATGTGGC[A/G]GTGTCAGACCATAGG	4067
rs539884421	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55896454	GTGGGAGCTGAACAA[G/T]GAGAACACATGGACA	4067
rs539907555	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55902553	TTTGACACCTGATCC[A/G]AAACACAGTCATGTA	4067
rs539915780	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56000985	TATCAAACACACAGC[C/T]ATCCTGTAGGGTGGT	4067
rs539919996	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55941134	GCCAGGTTCTGCAGA[C/T]TCTAGCTCTTCATCA	4067
rs539975463	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55948827	TTACTTATAAAATGG[G/T]AATGACAGTACCTAG	4067
rs540014302	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55902307	GCCATTGCGCCTGGC[C/T]GTAACAGTGTACTTT	4067
rs540076275	snp	C/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55891514	AGACAGAAAATAGAA[C/T]GGTGTCTTCCAGGGG	4067
rs540131435	snp	A/G	0.0566069	0.158427	intron-variant	LYN	GRCh38.p7	8:55942433	TGTATATATATATAT[A/G]TGTGTGTGTGTATAT	4067
rs540140266	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55914435	AAAAAGGAGAAGGCA[C/T]TTATTTGCTCATGTG	4067
rs540141749	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55935469	GTCCTTTTCAGTTCT[C/T]TCTCTTTTAAAAGTG	4067
rs540176312	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55929835	GATTTATTTATATCC[A/G]TGGATATGTTTTCCT	4067
rs540197319	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55922389	GCCACCACACCTGGC[A/T]GACATCACAATTTTA	4067
rs540209332	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55979086	TGAGATGGAGTTTTG[C/T]TCTTGTCACCCACGG	4067
rs540221863	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55969238	TAATCATGCCACTGC[A/G]CTCCAGCCTGGGTGA	4067
rs540223256	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55993073	TCTTAGATATTACAA[C/T]AGTTTGTGGCCCTCC	4067
rs540248510	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55907492	TTGGAAGGTGGTTAC[A/G]TGGGCACATACATCT	4067
rs540267184	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55954247	CTTGATCATCTGCCT[A/G]TTTCTTCATGATTCC	4067
rs540276429	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55961951	TTTTCTGACTTCTTC[C/T]TAATTTTGCCACTTT	4067
rs540282821	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55951212	CACGCCACTGCACTC[G/T]AACTAGCCTGAGTGA	4067
rs540292459	snp	C/T	0.00279162	0.0372561	intron-variant	LYN	GRCh38.p7	8:55901242	ATAGCAGTTACAAAA[C/T]GGGTAAGACTTCACC	4067
rs540320399	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55975602	CAGTACTTACATGTT[A/G]GGCACTTAAATGCTC	4067
rs540346049	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55980715	CCCTCTTTCCAGGCT[C/T]CACAAAGTAGGCAGG	4067
rs540361999	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55986892	CACTACACCCGGCTA[A/T]TTTTTAATTTTTTGT	4067
rs540413661	snp	A/G			intron-variant	LYN	GRCh38.p7	8:56007087	AAAAATCTGCTGTGG[A/G]GCTAGGGTGACCTAG	4067
rs540416052	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55995090	CTCCTCTCTCCCAGC[C/T]GCCACCAAAATTGCC	4067
rs540437500	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55889714	GCACCCAAATGAGTG[C/T]CCAGAAATCACTCTG	4067
rs540455298	in-del	-/G	0.115088	0.210473	intron-variant	LYN	GRCh38.p7	8:55939532	CTGCAGGAACGCAGT[-/G]GGGGGGGGGACAGGG	4067
rs540457877	snp	G/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55896594	AACCACCATGGCTCA[G/T]GTATACCTATGTAAC	4067
rs540462294	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55988798	TTGCTTGAGAGATCA[C/T]ATTCAGCCCCTCAGT	4067
rs540465891	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55980647	CAGAAGGGTGCCCAT[A/G]TCTTCCCAGGCAGCC	4067
rs540555218	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55896983	GACCTTAGGTGATCC[G/T]CCTGCCTTGGCCTCC	4067
rs540559504	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55997487	TGGCACCATATAGCT[C/G]TGTCCTCACGTGGTG	4067
rs540562253	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55924039	CATTCTCACTTTCTG[A/G]TGGTACTTGTTTTTT	4067
rs540566450	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55982108	GGGTGATGGGCTGGC[A/G]GATTCTTAACAAAGT	4067
rs540588512	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55914269	GATTGAGGACTCAGG[C/G]ACTAATCTAAGGGGA	4067
rs540617925	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55990430	TGAATGTCTCTTATG[G/T]GACCTTAAAAGGTGT	4067
rs540656706	in-del	-/AT	0.00478085	0.0486577	intron-variant	LYN	GRCh38.p7	8:56006310	AGCAAAGCTCAGAAA[-/AT]AATAATAGTAATAAT	4067
rs540658830	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55897865	CTGCAGTGAGTCGAG[A/G]TCGCGCCACTGTACT	4067
rs540663415	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55947264	CAAAAGAGAAAAACC[A/G]AAATGCTACATGATG	4067
rs540707832	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55985876	TCAGTCTTTTAATAT[A/G]CTAAGGGTGACCAGG	4067
rs540724360	snp	G/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55939621	GAGCTGGATCGAGCG[G/T]CCCGGTGCGCTGTGG	4067
rs540736822	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55940520	AGCTGGGACTACAGG[C/T]GTGTGCCACCACGCC	4067
rs540758802	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55983988	TTGGGAAGAATCCTT[C/G]CGTACCTCTTCCAGC	4067
rs540764513	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55892715	GCCTTGCCAAAGAAA[G/T]AATATTTCTGACACA	4067
rs540801078	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55977124	CAGAAGGCGGAGATT[G/T]CAGTGAGCCAAGATC	4067
rs540803412	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55886204	ATTGTTAAATTCCTT[C/G]TTAAATTCTTGGGAT	4067
rs540816591	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55973852	TTGGGAGGCTGAAAC[A/G]GGAGGATTGCTTGAG	4067
rs540827824	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55893414	GCATTTGAAAGTACT[A/C]ACTGGGTTTGTGAAT	4067
rs540835631	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55924596	CTTGAACTCCTGACC[A/T]CACGTAATCCACCCC	4067
rs540882542	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55879284	GGGAGGAAACTGAGG[C/G]TTTGAGAAACGGAGA	4067
rs540963776	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56006676	CTCTGCATGTCTCAG[A/T]GCTCAGTGCTAGTTC	4067
rs540971243	snp	A/T	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:56003562	AATCCTAGCTACTTG[A/T]GAGGCTGAGGCAGAG	4067
rs540973104	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	LYN	GRCh38.p7	8:56011371	ATTTTAATACACCTC[A/G]TCCAATAACATCTCA	4067
rs541036389	in-del	-/T	0.00398564	0.0444627	intron-variant	LYN	GRCh38.p7	8:55911603	TGAATTGGGGAAGTA[-/T]TTATACATATGTGAA	4067
rs541039898	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55898783	TGTCCTAGGCAGTCA[C/G]TAATCTATTTCTAGC	4067
rs541055714	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55944171	ATAAATTAACATTGT[A/G]ATTTTATATATAGAA	4067
rs541073026	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55970038	CAAGTCAACCTCTTT[A/T]TGTTCATTTCATAAG	4067
rs541081001	snp	A/G	0.00279162	0.0372561	intron-variant	LYN	GRCh38.p7	8:55884622	CACCATGCCTGGCTA[A/G]TTTTTGTATTTTTAG	4067
rs541084528	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55915355	TTTATTAAACTCTTT[A/C]AAAAAATACTTCTGT	4067
rs541096052	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55962917	ACACAGTGAGAGCAA[A/G]AGAGTGACCAGAAGA	4067
rs541119637	snp	G/T	0.000399281	0.0141238	utr-variant-5-prime	LYN	GRCh38.p7	8:55877412	CGCTTGGGGGCCATT[G/T]TAAACAGCAAAATCA	4067
rs541124747	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55936544	ACCTGGGAGGCTGAG[A/G]CAGAAGAATTGCTTG	4067
rs541131150	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55930900	CCAGTAATCCTCCCA[G/T]CTTGGCCTCCAGTGC	4067
rs541136953	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55937134	GAATATGTTGTGAAT[A/T]GTATAGTGTCTTCTT	4067
rs541144448	snp	C/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55923341	CCCTTCCCAGCACAT[C/G]TGCTCAGTTTCCGCC	4067
rs541213533	snp	G/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55977593	GGTGGGATGGAAAAG[G/T]AATGGGAGAGTTTGT	4067
rs541248278	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56002311	GTAGTCCCAGCTACT[C/T]GGGAGGCTGGGGCAG	4067
rs541271233	snp	G/T	0.0119091	0.0762411	utr-variant-5-prime, missense	LYN	GRCh38.p7	8:55879931	CAGCCCGCGGCAAGC[G/T]GGGCGGCCGCGCCAC	4067
rs541275791	in-del	-/A/AAAAAAA/AAAAAAG	0.0446223	0.143223	intron-variant	LYN	GRCh38.p7	8:55997928	CTCTACTAAAAATAC[-/A/AAAAAAA/AAAAAAG]AAAAAATTAGCCGGG	4067
rs541277586	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55956742	CTCACGTCAAGATCC[A/G]GGGACTTCTGCGTTC	4067
rs541323899	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55950031	CATACAATATGTGGT[C/T]CTTTTTGACTGCCTT	4067
rs541381826	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55902989	GAGTAGCTGGGACTA[C/G]AGGTGTGTGCCACCA	4067
rs541405232	in-del	-/CT	0.00318978	0.0398085	intron-variant	LYN	GRCh38.p7	8:55984063	TGCTCCTCTTCCCAC[-/CT]CTGTCTTCCGGTGGC	4067
rs541414714	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55996334	TCTTTTGCTAAGCAA[C/T]GTGGTCTGGAACTGG	4067
rs541423618	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55976266	CAGGAGGCAGAGGTT[A/G]CAGTGAGCCAAGATC	4067
rs541426623	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55943719	ATTACCCTGAAGGTA[A/G]GAAATATCTGCCATG	4067
rs541451434	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55989369	AGAAGTCCATCTGAT[A/G]TATTACCTAGGGCCT	4067
rs541494902	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55929957	GGAGGTGAACAGCAG[C/T]TGAGCAAGCATTACT	4067
rs541537963	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55990153	CTGAGGCAGGAGAAT[A/C]GCTTGAACCCAGGAG	4067
rs541558504	snp	A/G	0.00438332	0.0466095	intron-variant	LYN	GRCh38.p7	8:55897819	TCAGGAGGCTGAGTT[A/G]GGAGGATTGCTTGAG	4067
rs541579825	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55915827	AGAAGAGAGAAAGAG[A/G]GCGAGCGAGCGAGAG	4067
rs541588998	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55986502	AGGTAATTCTGTTTC[A/G]TGGACACTTAATGAT	4067
rs541595619	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55982735	GCTTCTCTGTGTCTT[C/G]ACTTCCTCCCCTCCA	4067
rs541653506	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55891918	ATACATGGCCACGTG[G/T]ATTGCTGGCTGACAG	4067
rs541675536	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55885646	TGGGTGCCCCCACTC[C/T]TCCTGTAAATGTTAA	4067
rs541676986	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:56002930	CATAGCACAGAAATC[A/G]GTAAACATTGCCAAA	4067
rs541679478	snp	C/T	0.00557542	0.0525036	intron-variant	LYN	GRCh38.p7	8:55934204	GCACTCCAGCCTGGG[C/T]GACAGAGCGAGATCC	4067
rs541767033	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55978656	CTGAGAGGGACAAGT[C/T]AGAGAGCAGGCTGGG	4067
rs541813282	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55895042	TGGTCTTGAACTCCT[A/G]GTCTCAAGCGATCTT	4067
rs541827469	snp	C/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55949425	ATTTTAATTCCATCA[C/T]GGAGAGTGAATTTTC	4067
rs541829048	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55903272	TGCTGGGATTACAGG[C/T]GTGAGCCACCGTGCT	4067
rs541844928	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55916627	TATAAATCCCTCACC[A/G]TGTCCTGAATTCCAC	4067
rs541850062	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55893074	TAAACAGATTTTCAA[G/T]CTGTGGGTTTGGCTA	4067
rs541902999	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55943263	GAATTCTGCAGCATT[G/T]AAGCTGGAAACAGTT	4067
rs541905386	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55911170	ATGTACATATATATA[C/T]ACGTATATATATATA	4067
rs541914062	snp	C/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55884226	CTGCCTCAGCCTTCT[C/G]AGTAGTTGGGATTAC	4067
rs541933458	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55927005	ACTTCCCACCCTCAA[C/G]CAGCTTATTATTAAC	4067
rs541945346	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55975534	GCAGATGACATTGAT[A/G]TAAGATTTTAGCATT	4067
rs541971423	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55987333	GAATTGCTCGAGCCC[C/T]GGAGGTGGAGGTTAC	4067
rs542019321	snp	C/T	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:55977057	GGGCATGGTGGTGTG[C/T]GCCTGTAATCCCAGC	4067
rs542032587	snp	A/T	0.0225045	0.103662	intron-variant	LYN	GRCh38.p7	8:56008130	CCTCAAAAAAAAAAT[A/T]AAATAAAATAAAATA	4067
rs542049404	snp	C/T	1.6522e-05	0.00287414	synonymous-codon	LYN	GRCh38.p7	8:55952090	CACTTTTCCCTGTAT[C/T]AGCGACATGATTAAA	4067
rs542051255	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime	LYN	GRCh38.p7	8:55877331	TTGAACTCCTGAGCT[C/T]GAGCAATCCTCCCAC	4067
rs542061222	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55962838	CATGGCACCTGTCTC[A/T]GCTTCTGGTGAAGCC	4067
rs542099220	in-del	-/C	0.00279162	0.0372561	intron-variant	LYN	GRCh38.p7	8:55959793	AAAATGTGGTGTATT[-/C]CATACAATGGAGTAT	4067
rs542145587	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55915768	ATAAAACATATGAAG[C/T]AGTGCTGCCAAAGAG	4067
rs542156034	snp	A/C			missense	LYN	GRCh38.p7	8:55953933	ATCCCCCGGGAGTCC[A/C]TCAAGTTGGTGAAAA	4067
rs542187929	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55991093	GCTGTGTCCATAGTG[A/G]CCTCTGAGATGCTGC	4067
rs542220608	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55982040	CTCTCCCTGGGCGCT[A/G]AACAGAGCCCTTTCT	4067
rs542226043	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55993598	TTAATTTCTCAAAGC[C/T]TCATTTGCATCTGTA	4067
rs542228055	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55972454	CCCTTGGCAACAAGG[A/G]GTAGGGCCTGTACGC	4067
rs542230816	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55941101	ATCTTCCTAGGCCCC[A/T]ACCTATGTTTAGCTG	4067
rs542268003	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55979083	TTTTGAGATGGAGTT[C/T]TGCTCTTGTCACCCA	4067
rs542289571	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55973016	TGTCACAATGAGAGA[C/T]TGGTCATTGGGAGTA	4067
rs542315050	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55900354	TATTTGTTGGGGGAA[A/G]AATAATCTTCCTCTT	4067
rs542329173	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55888411	TAACGAAGGGGAATC[A/G]CTGGAGCCTTTTAGT	4067
rs542353677	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55933354	CTGCATTTATTTAAC[C/T]AGTGACCTATAATTT	4067
rs542354415	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55922657	CTGTAATCCCAGCTA[C/T]TGGGGGAGCTGAGGC	4067
rs542364267	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55926533	GATCTCCCAGCTCTT[A/G]TCAGTTATTTTCTGA	4067
rs542379460	in-del	-/T			intron-variant	LYN	GRCh38.p7	8:55900715	AAGCAAAGCTAATAA[-/T]TTTTTTATAGCTAAG	4067
rs542391442	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55960000	GATGACTGGTTGCCT[A/T]GGGCTGGGGGGCCTG	4067
rs542399887	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55966574	GGTTTCACTGTTTTA[A/G]CCAGGCTGGTTTCGA	4067
rs542415857	snp	C/T	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55923298	GAGAGATAAAGCAGG[C/T]GGGTCCCGGTGCCAG	4067
rs542449819	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55882086	CCAGCACTGAGTTAC[A/C]CACATTTAGTGTGGG	4067
rs542452753	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55983856	ATTCCATTGAAAGCA[A/T]TGTATTAATTTCCTG	4067
rs542525702	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56005450	GTACTGTCCTGCCCT[A/C]GGCGCTGGCCTCCCT	4067
rs542552988	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55897108	GAACGATGTTACTCA[A/C]CCGAACGCTGGCTTT	4067
rs542561002	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55999387	TTTAAGTTTAAATAC[C/T]CAAGTAAGAACCACA	4067
rs542572804	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56009568	TCCCTGTGTCTTCAC[A/G]TGGTCTTTCCCCTAT	4067
rs542578717	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55953370	TATAAATTTCAGGCC[A/G]GGCTTGGTGGCTCAC	4067
rs542582364	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55924902	GCTGCAGTGCGGTGG[C/T]GCGATCGTGGCTCAC	4067
rs542636487	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56003129	CAGTGGCGTGATCTC[A/G]GCTCACTGCTAGCCC	4067
rs542685774	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, missense	LYN	GRCh38.p7	8:55879697	TTTCTGTGCCTTCAA[A/C]GCCCTGCGCGACGGC	4067
rs542694630	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55918059	AAGCAAGGCTGCACT[C/G]AGAAGGAACCAGGGT	4067
rs542701414	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55925754	TGAGGACACCCTGGA[C/T]GCTGGTGACTGGTAT	4067
rs542701983	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55957349	TTAATCATAAAACAG[A/G]GCCATAAATAATCCA	4067
rs542727863	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55931410	CTGAGCACAAAACCT[A/C]AGGGCCTCGAAACTC	4067
rs542736751	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55910769	AAATTGTTTTGCTTA[C/T]AGCTGAAGAGTCCCT	4067
rs542787453	snp	G/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:56004996	CACTATGTTGCCTAG[G/T]CTGGTTTCTAACTCC	4067
rs542814977	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55919938	TGGGAGCTTTGTCAC[A/G]TGACCCCACTCTTTG	4067
rs542852686	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55959514	TCTTTAGTAAGAAAA[C/T]ATGTCACATTAGTGC	4067
rs542856186	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55944861	GCAAACCCACACACC[A/G]CTTTTTCCTCTTGTT	4067
rs542866764	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55952892	TCCCTGTCTCCAGTG[C/T]CACTTTGCAGTCCTG	4067
rs542868706	snp	A/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55937369	TTTAAATATGTATAT[A/T]TAATTTTTTCAATCA	4067
rs542875440	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55984255	TTTGGGGGGACATTA[A/G]TTAATCCAGCACAGC	4067
rs542894051	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55951768	AATGGTATGTTGGCA[A/G]GCTACACAGCAAACA	4067
rs542896215	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55959086	ATTGACCGTGTGTAA[A/G]TGTTCCCTTTCTCCA	4067
rs542956909	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55905844	ATTAGGCCTGGAGTG[C/T]CTCCCATGCAAAGAG	4067
rs542960643	in-del	-/AT			intron-variant, downstream-variant-500B	LYN	GRCh38.p7	8:55968249	ATGTAACAATGCCTA[-/AT]ATATATATATATATT	4067
rs542971577	snp	A/G			intron-variant	LYN	GRCh38.p7	8:56005518	CCTGGGCTGAGTTGG[A/G]ATGGGCCGCCTTGCC	4067
rs543021947	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55987026	CGGCCTAAGTTGACC[A/G]TTTTTTAAATTATCT	4067
rs543029810	snp	A/G	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:55977632	CCAGAGCTCATCTCT[A/G]TCTGGCACAGTGGCT	4067
rs543042437	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55933075	TCTTGCAACATACCC[A/G]TGTAACAAACCTGCA	4067
rs543075422	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56003529	AAAAATTAGCCCGGC[A/G]TGGTGGCCAACGCCT	4067
rs543105331	snp	A/G	0.00318978	0.0398085	intron-variant	LYN	GRCh38.p7	8:55944529	CTTGTTGCCCAGGCT[A/G]GAGTGCAATGGCACC	4067
rs543128445	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55951299	AAGCACACATGATTG[A/T]GGCCAGTTCTTACCA	4067
rs543137993	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55971875	GAAGCTACTTTCTAG[A/T]CCTTCATAGCTTACG	4067
rs543163057	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55904640	CTGTAATCCCAGCTA[C/T]TCGGGAGGCTGAGGC	4067
rs543168570	snp	A/G			intron-variant	LYN	GRCh38.p7	8:56004694	TAGCGTTTGCTGCAT[A/G]TAGTTCTAAATATTC	4067
rs543181916	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55903185	TTTGGTAGAGACGGG[A/G]TTTCACCATGTTGGC	4067
rs543192499	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime	LYN	GRCh38.p7	8:56010757	AGGAGTGGCGTGCAC[A/G]TCTCTCTCTCTTCCA	4067
rs543193062	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55946569	GTGATTGTCCTAAAT[C/G]TTTTTATTTTTTTTT	4067
rs543211404	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55908399	ACAGGCACCCCCCAC[C/T]GCGACCTGCTAATTT	4067
rs543231166	snp	G/T	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:55887659	CTGTCACCCAGGCTG[G/T]ACTGTGATGGTGTGA	4067
rs543246729	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55880949	TTTTGTATATCCGAG[A/T]GTGTTAATTATCCCA	4067
rs543262432	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55986439	AGTTTTTGCAAGAGA[A/G]AGTAAATGGGTATTC	4067
rs543268919	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55937695	AGTGAGTTTTGTTTT[A/G]TTTTGTTTTGTTTTT	4067
rs543269181	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55913625	AAAGTGTAAACGCCC[A/G]TAATGGGCTTGGCAG	4067
rs543271629	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55991749	AGAGTTTTGGTCATG[A/G]TGCACCCCCACATGC	4067
rs543375565	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55893555	TTTATTTTTGTTGGG[C/G]GTGACAGAGAGAGGC	4067
rs543408761	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55893501	CAGCACCTTTGTTAC[C/T]GACTGTTATTTCAAC	4067
rs543419404	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55880419	GGCTCACCGCGTGTC[C/T]TTCCCGGTGAGGGCC	4067
rs543431218	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55937327	AAGTAATTGGCAAAA[A/G]CCGCAATTACTTTTG	4067
rs543434875	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55898949	CCTGCCTCAGCCTCC[C/T]GTGTAGCTGGGACCA	4067
rs543445749	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55970539	GGTGGTTTCATGAAG[C/G]CCAGTGTATGTAGCA	4067
rs543458216	snp	A/T	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55963480	TGGATGTTGTCACAG[A/T]AGCTCTGCAATTGAA	4067
rs543471974	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55886906	CTAGCTGTTTTGAAA[C/T]GCACAATAGTTAATG	4067
rs543498193	snp	C/T			upstream-variant-2KB	LYN	GRCh38.p7	8:55877143	TCACAACCAATAGCA[C/T]AGTAGCTCCTGCCTG	4067
rs543529361	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55916751	TACCCCATGCCCAAT[A/C]CTGCAATGGCACCTT	4067
rs543536822	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55898254	CATACTGTATGTGAT[A/C]GTTTTATTGTCTTTT	4067
rs543581681	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	LYN	GRCh38.p7	8:56011505	AAACTTGCCCAAGTT[C/G]TACCTCCTTCCTTTG	4067
rs543585540	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55957330	TGGTGTATTTTCCCC[A/G]ATTTTAATCATAAAA	4067
rs543604105	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55965833	TTATTAGAGAAAAAT[A/G]TTAGTCCTCGGCTGG	4067
rs543636770	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55941757	TATGATAAAGAATAA[A/G]AGTATATTTTTTCTA	4067
rs543662354	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55951187	AAGGGAGGCTGCAGT[A/G]AGCCGTGATCACGCC	4067
rs543669453	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55958823	GCTTAATGATATTCC[C/T]TTATATGCATACATA	4067
rs543732064	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55990542	ATGGCTTTGCAGGGC[A/C]GTTTCAAAATTTGTC	4067
rs543779790	snp	A/C	0.00716266	0.059414	intron-variant	LYN	GRCh38.p7	8:55920793	TCCCCACCACCCCCC[A/C]ACCGGGTTCCAGCAA	4067
rs543799975	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55983389	GCATTAGCGTTTTCC[C/T]TCACTTCTGCACTTC	4067
rs543806414	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55970989	TCAGAGCCTGCTGGT[A/G]GAAGCTGGGAAAACC	4067
rs543807318	snp	A/G	0.0023933	0.0345097	intron-variant	LYN	GRCh38.p7	8:55902935	CTCACTGCAACCTCC[A/G]CCTCTTGGGTTCCAG	4067
rs543808104	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55963786	AGAATTCTTTCTATA[A/T]CCTGGATGCAAGTTC	4067
rs543835430	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55885510	AAAACATCTGGTGGG[A/G]AGGTCTTCGTGTGGT	4067
rs543843628	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55901495	CCTTCTTTTGCACAC[C/T]TGTGGCCTCCCTGGA	4067
rs543859020	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56009771	AGGATGCTGTTCAAC[A/C]CCTAACAGCCTCAGT	4067
rs543864525	in-del	-/A	0.125182	0.216612	intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55923889	ACTTAGTGCCATTTG[-/A]AAAAAAAAAATACAC	4067
rs543866820	snp	G/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55964146	AAAAGGACCTAGGAT[G/T]GTTTTTTTTTGTCAG	4067
rs543873445	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55886003	AGTCTTAAGGGCAGA[A/G]CCTGCTTTGCGAAGC	4067
rs543873497	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55878280	GTGAGGACAATTTTG[C/T]GAGGAGTTAGGGAGT	4067
rs543893523	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55920977	GCTGGGATTACAGGC[A/G]TGAACCACCGCACCC	4067
rs543947337	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55910680	AGACATAATTTCTAA[A/G]ATATATTCAGGTTTC	4067
rs543948666	snp	A/G	0.00478085	0.0486577	intron-variant	LYN	GRCh38.p7	8:55989174	AGCTTGCTGGAAGCC[A/G]GTTTCACCGTGTGGG	4067
rs543975285	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55910156	TTTAGTTTAAGTAAG[G/T]CTCATTTGTCTACTT	4067
rs544101136	snp	G/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55997718	CTGATTTGAGAAACT[G/T]GCATAATAACATCTA	4067
rs544106019	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55991270	CAGCAGTGGGGGAGA[A/G]AGTCCTGCCCCTTTG	4067
rs544170984	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56005633	GTCTCTTAGCATCAT[C/G]AGAGATGGAGTTTAA	4067
rs544184177	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55977274	TAACTCTGGTTTAAA[A/T]AATGTATCTGTACAA	4067
rs544186923	snp	G/T	3.33389e-05	0.00408269	intron-variant	LYN	GRCh38.p7	8:55998549	ATTGTGTTTTATTTT[G/T]TTTTTGTCTGTTTTT	4067
rs544222417	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55882933	CTCTCAACTTATGAT[A/G]AGGCTGTGTCCCAAT	4067
rs544228648	snp	A/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	LYN	GRCh38.p7	8:55968217	TTCCTAATGATAGGT[A/T]TAAATATGAGTTTTC	4067
rs544257872	snp	C/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55883527	GCTGCTGTCCGAGCA[C/G]CCCTAGTGACTGTCT	4067
rs544286680	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55999645	ATTACTTCATCTACC[C/T]GATAGCAAAGAATAA	4067
rs544301081	snp	G/T			missense	LYN	GRCh38.p7	8:55999522	CTCCTATACGAAATT[G/T]TCACCTATGGGAAAA	4067
rs544311405	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55993046	AAATTGATCCCTTAG[G/T]GGTGATAAAAATCTT	4067
rs544325263	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55999980	CATCTCGAAACAAAA[A/C]AAAGACTTGATTTTT	4067
rs544328118	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55900234	GGAGTTGCAATGAAT[A/G]TTTAAACATTGCGTC	4067
rs544392318	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55901175	CCCTCTCCTTCCCCC[C/T]GTAATACTTTATGAA	4067
rs544406990	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55907396	ATTTCTGTGAAGTTC[A/G]GGAACAGGGTCATGA	4067
rs544408324	snp	A/C	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55890645	TTGTGTTCATAGTAG[A/C]ATTATTCACAATAGC	4067
rs544417761	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55908306	CTGGAGTGCAGTGGT[A/G]CAATCTCGACTCACT	4067
rs544426086	snp	C/T	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55997092	CTTGAACCTAGGAGG[C/T]GGGAGGTTGCAGTGA	4067
rs544437779	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55954884	AATAAAAGTTTTCAT[A/C]GTGAATGTGAACTTC	4067
rs544440389	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55901826	TCAAGTTGCATTTCC[C/T]GGCTCAACCAAAGAT	4067
rs544444440	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55994617	GCCCACCTGTGTGGC[C/T]GATCAACAGCGTTGG	4067
rs544449919	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55940731	AAGAACTGTGTCTGA[C/T]TCAAATGTTCAAAAT	4067
rs544484433	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55895473	GAGCAGCATGATGTC[A/G]TAGTCATAAACTGAG	4067
rs544514254	snp	C/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55927229	TGCCTTAAAAATCCC[C/T]CATTCTTCACATGTT	4067
rs544524108	snp	A/G	0.00478085	0.0486577	intron-variant	LYN	GRCh38.p7	8:55887312	AAAGAGCTGAACACA[A/G]ACTAGTAGATGACAT	4067
rs544576373	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55933990	CCCAGCACTTTGGGA[A/G]GCCAAGGCGGGCGGA	4067
rs544597070	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55911785	GATGAATTTGATTTG[A/C]AGATTGAGAAACAGA	4067
rs544635078	in-del	-/T	0.0023933	0.0345097	intron-variant	LYN	GRCh38.p7	8:55919097	TTGAATGTTGGTCTG[-/T]TGTTACCAGGAGATA	4067
rs544656099	in-del	-/AATAAAATATATTATATTTTTA	0.00318978	0.0398085	intron-variant	LYN	GRCh38.p7	8:55931135	TTACTTTTTATATAT[-/AATAAAATATATTATATTTTTA]AATAAAATATATTAT	4067
rs544669775	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55959575	CCAGGGTTTCCCACT[A/G]AATAGAAGTTGTTTG	4067
rs544696707	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55970767	TCGTGGGCTAAGCTG[A/G]CATTCAGCACCTGGA	4067
rs544707593	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55938918	CCTTTCTGAGCCTCA[A/G]TTTTCTCCTCTGTAA	4067
rs544730067	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55985588	TCTTTTCAGAATAAC[A/G]CACATCAAGTTCTTT	4067
rs544757460	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55927166	ATGGATTTTGACAAG[A/T]GTATAATGACATGTA	4067
rs544768259	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55979201	ACGTGTGCCACCACG[C/T]CCAGCTAATTTTTGT	4067
rs544783954	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55894905	GCTGGTTTCAATCTC[C/T]TGTGCTCAAGTGATC	4067
rs544825518	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55933520	GTGTGTACATTCTAA[C/T]GGAGTTTAATATGTA	4067
rs544832386	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55979761	AATGGTGTGTCTGGG[A/C]TCCTTGGTATGGTTT	4067
rs544834248	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55973176	CCTACTCTCCCCTCC[A/G]CATTCCCCTGTCACC	4067
rs544863809	snp	C/T	0.000971521	0.0220186	synonymous-codon	LYN	GRCh38.p7	8:55953935	CCCCCGGGAGTCCAT[C/T]AAGTTGGTGAAAAGG	4067
rs544881556	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55991582	GTACAAGATGCCAAG[A/G]GTTTCACCAGAACCC	4067
rs544943089	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55986379	TCTATCTTCGGGGTA[A/G]TACAGTGAGTTTTGA	4067
rs544956427	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55973604	GAGATGGAATCATAG[A/C]CATGTCAAACTGAGA	4067
rs544971089	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55968669	CTAAGTACTATTGTT[C/G]TGTGTCATAGATGAG	4067
rs544993528	snp	A/G/T	1.78115e-05	0.0029842	intron-variant	LYN	GRCh38.p7	8:55966691	TGTTTTATAAAGCAT[A/G/T]CCCGCCTTCTTTTTT	4067
rs544996740	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55888498	TATGGCATTTATGAC[A/G]TAGCCAAGAGCGAAG	4067
rs544996980	in-del	-/A	0.00318978	0.0398085	upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55878781	AAGGAATTAGTATGC[-/A]AACTTTAGTACTCTT	4067
rs544999355	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55947919	TTCCTTTTAAGTCGG[C/T]CTGTGAGCACACTTC	4067
rs545014785	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55904735	AGCCTTGTAACAGAG[C/T]GAGACTCCATCTCAA	4067
rs545027663	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55918877	TCTCCACCTTCACGG[A/T]GGTGGTACCCAGGGG	4067
rs545047761	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	LYN	GRCh38.p7	8:56012334	CACACCTCAGGTTAT[C/T]GTAGAGAACTGGAAA	4067
rs545060029	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55882217	TGGCCCAATCCAGAA[C/G]ACCTACATTATTTTA	4067
rs545064639	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55920033	CTCAGTGACAAAATC[A/G]GAGAAAAAAGTCAAT	4067
rs545119080	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55951385	GACAAAGAAAATTAG[G/T]CTGGGCGTGGTGGCT	4067
rs545124270	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55905192	GAGGCAGGCGGATCA[A/C]CTGAGGTCAGGAGTT	4067
rs545161489	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55912714	TCTGGGTGACAGAGT[A/G]AGACTCCATCTGAAA	4067
rs545169973	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55887761	ATTACAGGCACACAC[C/T]ACCATGCCCAGCTAC	4067
rs545179869	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55913422	GGGCCCAAGAATCTA[C/T]ATTTTTAACAAATAC	4067
rs545244471	in-del	-/T	0.00318978	0.0398085	intron-variant	LYN	GRCh38.p7	8:55907559	TTTCATTGTAGGTGC[-/T]TTTTTTTTGGTGGAA	4067
rs545249356	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55896078	TTAGCTCATCCTTAA[A/G]CATCTCGTTAGGGGT	4067
rs545260363	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55993124	ACAACCTTCTTTCCT[C/T]ATGTTTAATTTCTCC	4067
rs545266123	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55992331	GAGGCCTGACCCTGT[A/G]TCCCCTGCCTCCAAG	4067
rs545312676	snp	A/C	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55901287	AGGAAAATTGATAGA[A/C]TTCCTCCACCTCCTT	4067
rs545322344	snp	C/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55901219	TTCTGAATAGTTCTC[C/T]GATTAGAATAGCAGT	4067
rs545341988	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55894798	CCTCAGCCTCCCAAA[G/T]TTCTGGGATTACAGG	4067
rs545380103	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56001546	TGCCTGCACAGTGGA[C/T]CGGCTGTCCCAGGAA	4067
rs545402665	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55965740	TATGCCTGTGTGTGT[A/T]TGTATATGTATGTAA	4067
rs545446932	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55951836	GACTTTTAAAATTAT[A/G]CATTTTATACAAATT	4067
rs545507532	snp	A/G	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:56004483	ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT	4067
rs545507568	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55945737	AATAACTCACCCCCC[C/T]ACTGAAATAACAGGG	4067
rs545517918	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55886133	AAATCTTTTAATGTT[C/T]AGGCTACATAATAAT	4067
rs545523359	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55902907	AGGCTGGAGTGCAGC[G/T]GCGCAATCTCCACTC	4067
rs545554981	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55904742	TAACAGAGCGAGACT[C/G]CATCTCAAAAAAGAA	4067
rs545583538	snp	C/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55894226	TATTATTTTAGACAG[C/G]GTCTTGTTCTGTTGC	4067
rs545631243	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55935525	ACGCCTGTAATCCCA[A/G]CACTTTGGGAGGCCG	4067
rs545659381	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55976290	CAAGATCACACCACT[A/G]CATTCCAGCCTGAGT	4067
rs545683890	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55891276	AGAATCACTTGAACC[C/T]GGGAGGCAGAGGTTG	4067
rs545692972	snp	C/T	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55930031	TCATAGGGGCGTGAA[C/T]CCCATCGTGAACTGC	4067
rs545734587	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55915712	ACTCCGTCTCAAAAA[A/G]TAATAAAAAATTAAG	4067
rs545745997	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55987030	CTAAGTTGACCATTT[G/T]TTAAATTATCTGACT	4067
rs545769208	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55994808	GGCTGCACTACCATG[A/G]AGTGGAGCCGGGAGG	4067
rs545793463	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55955156	CGTCACCTCTGCATC[C/T]AGGTTTTCCCTCTAC	4067
rs545809273	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55980880	ACCAACATCCACCTG[C/T]AGAACTCTTTCATCT	4067
rs545818775	snp	A/T			intron-variant	LYN	GRCh38.p7	8:56003275	GCCGTGTTAGCCAGA[A/T]TGGTCTCGATCTCCT	4067
rs545822355	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55948965	ATCCTGTCTGTGTGT[G/T]GAATTTATAGAGGAA	4067
rs545854240	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55955733	CTTTCTGTCTCTATG[A/G]ATTTAACCACTCTAG	4067
rs545866352	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55949329	GAGCCATTTGTACCA[A/C]CTCTTCTTTGTGCAC	4067
rs545891761	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55914777	TAAAATAAGAAAGGC[C/T]AAGGAAGTTGCTCTT	4067
rs545923194	in-del	-/T	0.00279162	0.0372561	intron-variant	LYN	GRCh38.p7	8:55963163	GGCTGCTATGAACAA[-/T]GCGCTGCACATTTTT	4067
rs545924180	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55981412	ATGACTATACTGGCC[A/G]CTTAAAATGGGGATT	4067
rs545924468	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55918047	GAAGAGCTGACTAAG[C/T]AAGGCTGCACTGAGA	4067
rs545972960	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55982182	TGTCTGTAACATCAT[C/T]ATCTGGCAATGTTAT	4067
rs545975336	snp	A/T	0.00557542	0.0525036	intron-variant	LYN	GRCh38.p7	8:55989320	GATTTGTAAAACATA[A/T]TTGAGATTGTGCTCT	4067
rs546016032	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55943213	TGTATTCTCTCACTG[C/T]ATACATGTATACCAC	4067
rs546027461	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55981518	TATTTTTTGTGTGTT[C/T]AAAAAAATTTTTTTT	4067
rs546034370	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55975693	TTAGAAAATGGACAA[A/G]TGAAACTAGTTACTG	4067
rs546036245	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55953697	CAAAAGTCACAATTA[C/T]GTCAAGGATGCATTT	4067
rs546036358	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55982676	TCCCAGCACAGCCCT[A/G]TCATCATTCCATCAT	4067
rs546077718	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55935948	CCCCATGTCACTTTG[A/G]TAAGCAGTTTGGAGA	4067
rs546085190	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55969485	AAGTGGTATCCACCC[A/T]CATTCTTTCTCACCT	4067
rs546093003	in-del	-/T/TTTCT	0.413914	0.188765	intron-variant	LYN	GRCh38.p7	8:55902331	TACTTTCTTTCTTTC[-/T/TTTCT]TTTTTTTTTTTTTTG	4067
rs546118686	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55973824	AGTGGCATGCACCTA[C/T]TGTCTCAGCTACTTG	4067
rs546137907	snp	A/C	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:56001025	GTGGAGCCTGCGTGG[A/C]GTGGCTTAGGGATTG	4067
rs546167638	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55895615	GGCATCATAGTGAGA[A/C]CTCATCTCTACAATT	4067
rs546212135	in-del	-/GT			intron-variant	LYN	GRCh38.p7	8:55892784	TTTCCCAATGCAGGA[-/GT]GTGTGTGTGTATGTG	4067
rs546231913	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55906815	GAGGTGTAAGCCTCC[A/G]GATGAAGGAAGAAGG	4067
rs546310741	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55940857	GTGTTGTTCTGCCCT[G/T]GTCAGGCACCAGCCC	4067
rs546321089	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55928134	GTAGTAGAGTATATC[A/T]CATTGTTGCTTGGTT	4067
rs546337253	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55904053	CTTGGAGTTTCAAAC[A/T]TAAAGTAGAATTACT	4067
rs546387634	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55979532	TGTAGCTCTGCAGCT[C/T]GTGGGGCTTTGTGAA	4067
rs546418745	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55934631	CTGGCTGTTTTGTCT[C/T]GACACCCCTTTCCTC	4067
rs546436159	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55981091	ATGTGACTGATTCCT[C/T]AGCACTGAGCCCACC	4067
rs546512919	in-del	-/ATTTTTTCTTTCATGGATC	0.00358779	0.0422022	intron-variant	LYN	GRCh38.p7	8:55928754	GAAGTTCAATTTATA[-/ATTTTTTCTTTCATGGATC]ATTTTTTCTTTCATG	4067
rs546523383	snp	A/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55968793	TATAGCCTCTAGTAC[A/T]TGCCCATTTTACAGA	4067
rs546547661	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55985773	GACCTGCAACTGGGT[A/G]GGGCTTGTGGCATAC	4067
rs546583430	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55921818	GATGGTATATTAGTA[A/G]TAATAATGTTTAAAA	4067
rs546601281	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55993337	TGAGGGGTGAAATTT[A/G]TACTTAACAACAATG	4067
rs546611805	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55891848	TACCTACCAAGCAGA[C/T]GGGTGTTCACTTTTT	4067
rs546618137	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55945710	GGTCTTCTGTGCCAC[C/T]AAATCCTTCCCAATA	4067
rs546632874	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55948118	AGCTAGGACTACAGG[C/T]ATGTGCCACCAGGCC	4067
rs546699388	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55986688	TGAGCTATGAAGGTA[G/T]TCTAACAGACTGCAA	4067
rs546699730	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55979375	GTGGTTTTCTTCTGT[C/G]ATGGAATAAAATGAA	4067
rs546725428	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55888673	TCTGCAAGTAGGTAC[C/T]TGACACCTCCCCTAA	4067
rs546727741	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55952168	TTTGTTATGATATGT[A/G]TAAGACGTCAAACGC	4067
rs546740013	snp	A/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55949560	CACTTTTTTCCTTTT[A/T]TTTTTAGTTGACATG	4067
rs546743931	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55895682	GTCAAATACCAGTCT[C/T]GGGACATTAGATGAA	4067
rs546771506	snp	G/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55933582	CTCATGCCAAGCCCA[G/T]TGATTTCATTTTATG	4067
rs546795012	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55947956	TTTCCCTTTGAAGAC[A/G]GACAGTGGTTTTTCT	4067
rs546810436	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55973220	AGTGGCTAAGTGCAC[A/G]TGACAGCCTCACAGT	4067
rs546907806	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55975138	GATTCAGGGGCCACA[C/T]AGTGGTCAGGATGTG	4067
rs546943941	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55982804	ACCAATTCTGCTGCT[C/T]ATTGCTTCATTTGAT	4067
rs546950727	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55929743	TACAATACACAGAAC[A/T]GTCCTCTAGAACAAA	4067
rs547013263	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55884967	TTACACTCAGGATAC[A/G]GTTTTCCTTGGTATA	4067
rs547033373	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55975988	CAAGATCTGTCTCTT[A/G]TCTTAATGTTATTTT	4067
rs547049080	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55939084	GTTTTTGTCAGGAGT[A/G]TATTGTATTTTCTAC	4067
rs547062240	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55926195	CGTAGATTTACCCCC[A/C]AGATCCAACCACTTC	4067
rs547092625	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55970313	TATTTTTAGTACTAG[C/T]CTAGGAGTTGCCTGT	4067
rs547153174	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55917010	GGTGAAACCCCGTCT[C/T]TACTAAAAATACAAA	4067
rs547164052	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55923760	GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCAA	4067
rs547222139	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55967513	TAGAGATGGGGTTTC[C/G]CCATGTTGGCCAGGC	4067
rs547229288	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55999264	GGTGAAGGTTGCAGT[A/G]AGCCGAGATCGCATC	4067
rs547247020	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56003163	CTCCCGGGTTCACGC[C/T]GTTCTCTTGCCTCAG	4067
rs547270859	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55910302	ATTTAAGTCTTTAAT[G/T]CATCTTGAGTTGATT	4067
rs547289443	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55960597	ACTGAAGGATACTCC[A/C]TCTCCCAATTTTGAG	4067
rs547298177	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55998006	GGAGAATGGTGTGAA[C/T]CCAGGAGGTGGAGCT	4067
rs547310254	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55906111	CTGGGATGGTGAGGT[C/T]GCCCTGTAAACTCTG	4067
rs547320327	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55961629	CTAACCTTGGAAAGC[A/G]TTTTTTTTCCTTCGT	4067
rs547330253	snp	A/G	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55910917	TTTTTTTTTTTTTGA[A/G]ACAGAGTCTCGCTCT	4067
rs547333127	snp	C/G			utr-variant-3-prime	LYN	GRCh38.p7	8:56010619	GATTTTGCAGGTGAA[C/G]TCAGCAGCTTAAAAA	4067
rs547355470	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55917464	GCTGGGATTATAGGC[A/G]TGAACCACCAAAAAC	4067
rs547383149	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55969608	ACAGAATTGCAAAGC[C/T]AATCATTTTGTGGGG	4067
rs547387604	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55976616	CCTGGGATATGGCAA[A/G]GGCTGTCAGAGTGGG	4067
rs547458956	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55930140	CTGTGGAAAAATTGC[C/G]TTCCATGAAACCAGT	4067
rs547465450	in-del	-/AG	0.00358779	0.0422022	intron-variant	LYN	GRCh38.p7	8:55915779	AAGCAGTGCTGCCAA[-/AG]AGAGAGAGAGAGAAA	4067
rs547471094	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55924185	AGTGAGTACCTCTCA[C/T]GATGTGTGAGAGATG	4067
rs547477641	in-del	-/G	0.00478085	0.0486577	intron-variant	LYN	GRCh38.p7	8:55910953	CCAGGCTGGAGTGCA[-/G]TGGTGCAGTCTTGGC	4067
rs547499505	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55970672	GCCTTCTTGGGAATA[C/T]GAGATCCAAGGAATG	4067
rs547519838	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55995084	GCAGGGCTCCTCTCT[A/C]CCAGCCGCCACCAAA	4067
rs547530005	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56001121	ACTCACAGAGGGAGG[C/G]AGTCTTGGGCTCTCT	4067
rs547546661	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55955345	AACTGTAATTACATG[A/T]CTTCACATTCTCCGT	4067
rs547624164	in-del	-/T			intron-variant	LYN	GRCh38.p7	8:55891790	GTGTCCTTGAGGATA[-/T]TTCATTAAGTTTGAT	4067
rs547647339	in-del	-/T	0.00358779	0.0422022	intron-variant	LYN	GRCh38.p7	8:55969665	TGAATTTTGTTTGGA[-/T]TTTTTTCTTGTGTGT	4067
rs547738698	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55922754	CCTGGGCAAAAAGAG[C/T]GAAATTCCATCAAAA	4067
rs547745199	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55884279	CCAGCTAATTTTTGT[A/G]TTTCCTGTAGAAATG	4067
rs547755002	snp	C/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55971719	TTGTAAGACTTTATC[C/T]TGACATAGTCAAAGC	4067
rs547772634	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55989051	TCCAAAGCATTGCTC[A/T]TGTTCTCTGGTGGTA	4067
rs547779277	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55897230	AGTACATTAGAACTT[G/T]GATTCATGTGACGCC	4067
rs547804568	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55897114	TGTTACTCACCCGAA[C/T]GCTGGCTTTATGCAG	4067
rs547920787	snp	C/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55935159	ACTGTTCCTATTACA[C/G]ATGACATTTAAACCT	4067
rs547934849	snp	C/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55929030	ATACAGTTGTTCCAG[C/T]ACCACTTATTGAAAA	4067
rs547949907	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55908643	TGCAGTTTTGTTACA[C/T]GGATATATTGCAGAG	4067
rs547953190	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55995502	TCCTGCTGTGCTTAG[C/T]GCTGTGCTGTGCTCA	4067
rs547989769	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55936758	ATATTCCAAATAGCC[A/G]GAAGAGCAAATTTTG	4067
rs548010636	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55896547	CATTAGGAGAAATAC[C/G]TAATGTAGATGACGG	4067
rs548058868	snp	A/G	0.000233089	0.0107931	intron-variant	LYN	GRCh38.p7	8:55942024	GGGGAGAATTCCCAC[A/G]GCAAGATCAAAGCAT	4067
rs548073520	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	LYN	GRCh38.p7	8:55924165	GTTGAAACAGCACTA[C/T]CTTGAGTGAGTACCT	4067
rs548075025	snp	A/G	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55916008	TTAATATTTTAAAGG[A/G]TAGCCATTGTTTTAA	4067
rs548087147	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55916876	GCTATTTTTTTTTCT[C/G]TTTTTTAAAAACAGA	4067
rs548094454	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55963094	GGATCAAATTTCAAC[A/C]TGAGATTTGGAGAGG	4067
rs548100531	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56008453	TTGCATGACATACAT[G/T]CTTCTCTAGAGAAGT	4067
rs548138722	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56002117	AAAACCCCATCTCTA[C/G]TAAAAATATAAAAAT	4067
rs548163853	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55913994	CTCTATCAGATGAGC[A/G]ATGAGCAGTGAGGAA	4067
rs548176079	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55967680	GTGTTCAGGGTGTCA[C/T]TTTTAAATATTAATG	4067
rs548188914	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55941660	GATGGAAAATTAATG[A/C]TCAATAAATATTTGT	4067
rs548234589	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55929331	CTTAGTGAGACTAAG[A/C]ATACAGTCGGGATGA	4067
rs548268884	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55883219	AATGCCTAATGCTTT[C/T]GCACCATCGTAAAGT	4067
rs548273592	in-del	-/T	0.00358779	0.0422022	intron-variant	LYN	GRCh38.p7	8:55880343	CGCGGGGACTGAGGC[-/T]CCGCAGGTGTCCGCC	4067
rs548340197	snp	C/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55975814	ACTCTTTTTTTTTTT[C/T]GGTAAGGTGGGGGTG	4067
rs548351760	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56001058	GAGTACTCACAGAAG[C/G]GGGTGGGGAGCTGCT	4067
rs548365185	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55961607	ATATTTCCTGATGAC[G/T]TCCCCCCTAACCTTG	4067
rs548391134	snp	C/G/T			intron-variant	LYN	GRCh38.p7	8:55907798	TTGGGCCTGGGAGGT[C/G/T]GAGGCTGCAGTGAGC	4067
rs548415634	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55970609	TAGTCTTCCTTTTTC[A/G]CTGCCACTTCTTCCC	4067
rs548420244	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55997850	AGCACTTTGGGAGGC[C/T]AAGGCGGGCGGATCA	4067
rs548420513	snp	A/G	0.00636936	0.0560724	intron-variant	LYN	GRCh38.p7	8:56009402	CTATATTAGTTGGCA[A/G]GGGCTGCCATAACAA	4067
rs548438709	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55963605	TACCAGACTTTAAAA[A/T]TTTTTGCTGAGCTCG	4067
rs548444518	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55989273	CATCACTAGGAAGCT[A/G]CTAAGCAGGGGCATT	4067
rs548459846	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55902077	CAATGGTGCGATCTT[C/G]GCTTACCACAACCTC	4067
rs548466619	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55956440	TCTTAATGATGTTCT[A/G]TTTGATTTTATCTAC	4067
rs548468502	snp	C/T	0.00358779	0.0422022	intron-variant	LYN	GRCh38.p7	8:55907684	CCAGCCTAGGCAACA[C/T]AGGGAGACCCTGTTT	4067
rs548515906	snp	C/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55902426	TCCGCCTCCCAGGTT[C/G]AAGCAATTCTCCTGC	4067
rs548557434	snp	A/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55890124	TCTATAGACAAAAAA[A/T]AAAAAAAAAAAAAAG	4067
rs548572282	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55960769	TTGTTCATGGACAAC[C/G]CATTTCATTTTATGG	4067
rs548581740	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55965153	CTTTCCCAAGAGAAA[C/G]TCAGGATTAAAGTGC	4067
rs548678446	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55939539	GAACGCAGTGGGGGG[C/G]GGACAGGGGATTCCC	4067
rs548698878	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55887099	GATACTTTGTAAATA[C/T]CTTAAAAGATAAAAC	4067
rs548708360	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55961241	TCAAGGTGCCACATC[A/G]GCTTTCTTTAACTGT	4067
rs548712716	in-del	-/T	0.039522	0.134904	intron-variant	LYN	GRCh38.p7	8:56003226	ACCACGCCCAGCTAA[-/T]TTTTTTTTTTATTTT	4067
rs548712729	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55936476	GAAACCCTGTCTCTA[C/T]TAAAAACACAAAAGT	4067
rs548718121	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55880182	GGCTGTGCCACCAGC[C/T]GGAGTCCCGGGCGCA	4067
rs548719191	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55921790	CAGGAGTGTTGATAG[C/T]AGTATTACAAATGAT	4067
rs548754177	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55962200	AATTCATTCATCTTC[A/G]TTCCATATGGTGTTG	4067
rs548768495	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55985027	GGCCCTGAATAAGCC[A/G]CAGGGGTCCTGTGGG	4067
rs548768797	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55955274	GAGCCAGCCTATCAT[C/T]AATTAATTCTTACTG	4067
rs548845304	snp	G/T	0	0	intron-variant	LYN	GRCh38.p7	8:56004298	AGAAAGACTTCCTTT[G/T]TTTTTTTTTTTTTGA	4067
rs548849929	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55968598	TTACTATATGCCAGA[C/T]TGCTCTTGGTGCTTT	4067
rs548868424	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55949055	CTTCCAGTGCTCATC[C/T]CTGCCTCCTCCCTGG	4067
rs548880271	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55970753	TCTGTAATAGAGCAT[C/T]GTGGGCTAAGCTGGC	4067
rs548885964	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55998015	TGTGAACCCAGGAGG[C/T]GGAGCTTGCAGTGAG	4067
rs548911482	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55985087	GAAGTTGCTGAACCG[A/G]GCAAGTGATCCTTTT	4067
rs548940776	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, synonymous-codon	LYN	GRCh38.p7	8:55879479	GTTGGAAGGGATCAG[A/G]GCGCACCTCCTCCGC	4067
rs548951262	snp	C/T	6.5912e-05	0.00574035	synonymous-codon	LYN	GRCh38.p7	8:55951997	TGTCAGAGACTTTGA[C/T]CCTGTGCATGGTGAT	4067
rs549015230	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	LYN	GRCh38.p7	8:56010812	CAGCTGCCCTGTCTG[C/G]TCACCCGAAGGCACC	4067
rs549018207	snp	C/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:56003796	CATTTTTAGAGGAGA[C/T]AGAAATACTAAGATA	4067
rs549032434	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55958042	GTGCGTCCTGCAGGG[G/T]GTGCCTGGCGAGGTT	4067
rs549037411	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime	LYN	GRCh38.p7	8:56010940	AATTTCCTATATCCA[G/T]ATTTGTTTTGACAAT	4067
rs549055040	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55899888	TCAGGCAATCCACCC[A/G]CCTCGGCCTCCCAAA	4067
rs549061500	snp	G/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55932592	CGCCTGGCTAATTTT[G/T]GTATTTTTAGTAGAG	4067
rs549104544	snp	A/G	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:55997856	TTGGGAGGCCAAGGC[A/G]GGCGGATCACGAGGT	4067
rs549165330	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55913122	CTCATATCCAAAAAC[C/G]TTTTTGCAAAAATCA	4067
rs549229114	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55936358	GAAGTGCAGCTTTTA[A/G]GCTGGGCGTGGTGGC	4067
rs549255656	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55982913	TCACCAGCACTTCCC[A/G]TCCCTTGAACCTGCC	4067
rs549298063	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55971268	CCCTGGGAGGCTCCA[C/T]GGGATTCCAAGGTTT	4067
rs549317933	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55938353	CATAAAATATGTCTT[C/T]ATTTACTGTTCAAAA	4067
rs549341961	snp	A/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55956953	GTGTTTGCATTGACA[A/T]TCTCACTTACTCATT	4067
rs549348796	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55885805	AAAGGCCCCAGAGGA[C/G]GCAGGCAAGGAAGTG	4067
rs549379028	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55971203	AGAGGGGCAAGGAAA[G/T]GACCCAGCAGCCCTG	4067
rs549385376	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55886272	TTGAGATGGAGTCTC[A/G]CTCTGTCGCCCAGGC	4067
rs549402800	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55901415	AATATGAAAGGAACT[A/G]TTTAATTGAACGGTT	4067
rs549424174	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55879402	TAATGATTATTAAGA[A/G]CTCAGCGAGACCCCG	4067
rs549447146	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55977710	CTGAGGCTGGGAGTT[C/T]GAGCCCAGCCTGGGC	4067
rs549463676	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55970715	GGTGAAGCACCTCAC[C/G]TAAGGTAGGGCTGGA	4067
rs549465086	snp	A/G			utr-variant-3-prime	LYN	GRCh38.p7	8:56010737	AGACCTGCTAGACAT[A/G]CCATAGGAGTGGCGT	4067
rs549474684	snp	G/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55936959	AAGTAGGCACATACG[G/T]GTTTATCCCTTTTCT	4067
rs549481655	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55958051	GCAGGGGGTGCCTGG[C/T]GAGGTTGGGAGCAGG	4067
rs549505809	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56003280	GTTAGCCAGAATGGT[C/T]TCGATCTCCTGACCT	4067
rs549522024	snp	A/G			intron-variant	LYN	GRCh38.p7	8:56008381	AGAGATAGCTATGGA[A/G]AGGAAATTCGTTGTG	4067
rs549559979	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55892398	GGACTCCTGCCTGGG[C/T]GACAGAGCAAGACTC	4067
rs549585198	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55936812	ATACATTAAAAATAA[A/T]AAAAGCAACAAAAAA	4067
rs549610572	snp	C/T	0.00318978	0.0398085	intron-variant	LYN	GRCh38.p7	8:55917108	CCTGAACCCAGGAGA[C/T]GAGGCTGCAGTGAGC	4067
rs549611081	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55899473	ATTAACATAAATGTA[A/C]ACGCAGGAATAAGAC	4067
rs549628480	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55997822	AGGCGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC	4067
rs549641428	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55981944	GCCAACGGCAGATGC[A/G]TTCTGCTTAATTTGG	4067
rs549644505	snp	A/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55931177	AATATATTATATTTT[A/T]AAATATAATATGTAA	4067
rs549703253	snp	A/C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55924612	CACGTAATCCACCCC[A/C/G]CTTGGCCTCCCAAAG	4067
rs549710469	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55898653	AAAGTATACAATTCA[A/G]TGATTTTTAGTATGT	4067
rs549710499	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55904755	CTCCATCTCAAAAAA[A/G]AAAAAAAAGAAGATA	4067
rs549714856	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55957915	ATTGCGCCGCTGTCA[C/T]CAAACTGGGTGACAG	4067
rs549719997	snp	A/C/G			intron-variant	LYN	GRCh38.p7	8:55984551	TCCTCAGCAAGTCTG[A/C/G]GGTTCTACCCTCAAA	4067
rs549731353	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	LYN	GRCh38.p7	8:56010260	TTACTCAGGAAGAAC[A/G]CCCTCTAAATGGGAA	4067
rs549756687	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55960863	AAGGGGCTGGGTGGG[A/G]ATAAAAGAAAGAGGT	4067
rs549770778	snp	C/T	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55990965	TGTCCCCACTCTGCC[C/T]AGCTTAAGTGTGTGC	4067
rs549770853	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55999398	ATACCCAAGTAAGAA[C/T]CACATATCTTCTTCC	4067
rs549774392	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55944557	ACCATCTCAGCTCAC[C/T]GCAACCTCCTCCTCC	4067
rs549799776	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	LYN	GRCh38.p7	8:56010222	ATCATCTGCCGTGCC[C/T]GGATCCTGAAATAGA	4067
rs549825492	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55965229	AGGAGTCAGTATTGC[C/G]CAGAGCGTGTTCCAT	4067
rs549827285	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55949637	TGTATGCAGTGTGTA[C/T]GGATCAAGTCAGCGT	4067
rs549875059	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55964359	CACCTTGTCTAGCCT[C/T]ATTTTTCTATAGAGC	4067
rs549892177	in-del	-/AAATTAAATT	0.0523655	0.153103	intron-variant	LYN	GRCh38.p7	8:56002605	GAGACTCCATCTCAA[-/AAATTAAATT]AAATTAAATTAAATT	4067
rs549902428	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55924606	TGACCTCACGTAATC[C/T]ACCCCCCTTGGCCTC	4067
rs549920521	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55910990	CAACCTCCGCTTCCC[A/G]GGTTCAAGCGATTCT	4067
rs549955082	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55895472	GGAGCAGCATGATGT[C/T]GTAGTCATAAACTGA	4067
rs549993902	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55957544	TGAAGCCAGGATAAA[A/G]CATCAAATTGCATGC	4067
rs550037459	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55982854	GCCTCCCTTCTGTCC[A/G]CTCACCCTCCTGCAG	4067
rs550050046	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55991480	GATGACTGGAAGTCT[A/G]TCTATCCAGCCAAAC	4067
rs550056762	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55989148	CAGAGCCTGCGCCTC[A/G]GGTGGGAGAGAGCTT	4067
rs550088259	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55898893	GCAGTGGCACAATCA[C/T]GATCACTGTAGCCTC	4067
rs550098770	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55976636	GTCAGAGTGGGCACC[A/G]CATGCTACTTTCAGA	4067
rs550133061	in-del	-/T	0.0023933	0.0345097	intron-variant	LYN	GRCh38.p7	8:55948140	ACCAGGCCTGGCTAA[-/T]TTTTTAAAATTTTTG	4067
rs550145489	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55924322	TGTTCTATACCATCT[C/G]TTTTCCTTCTCAATT	4067
rs550153575	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55952307	CTCACGCCTGTAATC[C/T]CAGCACTTTGGGAGG	4067
rs550154535	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55877864	CATCAATCAATTAAC[C/T]AATCAATCAATACTA	4067
rs550195522	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime	LYN	GRCh38.p7	8:55877617	GTATTGATTTTGAGA[C/T]TACAAATACATTTTA	4067
rs550229427	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55946800	TGTCTTTATGAATTT[C/T]ACTACTCTAGGTACC	4067
rs550236570	snp	C/T	0.00279162	0.0372561	intron-variant	LYN	GRCh38.p7	8:55939634	CGGCCCGGTGCGCTG[C/T]GGGTTGGCCGCACCC	4067
rs550249062	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55967062	ATAAACCTAATCACC[A/G]GAAGTAATCCATGTC	4067
rs550309049	in-del	-/G			intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55922277	AATTTTTTATAGAGA[-/G]GGGGGTCTCACTGTG	4067
rs550367825	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55897875	TCGAGATCGCGCCAC[C/T]GTACTCCAGCCTGCG	4067
rs550387593	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55906062	GTAGTTCATCTGATA[C/T]GTGCAGTTACGCAGC	4067
rs550402547	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55936326	ACAGAAAGGCAGCAA[A/G]ACCTTGCATCAGTAA	4067
rs550417738	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55919069	TAGTCAGACATTCCC[A/G]ACAGGCAGGACTGTT	4067
rs550480603	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55892262	CCCATCTCTTCTAAA[A/G]ATCCAAAAATAGCCA	4067
rs550520129	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55899257	ATATTGATATTCTTG[A/T]TATTGATAAGGAAAC	4067
rs550526792	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55980062	CAGGCCACAGTCCCC[A/G]GGAGGTGGCCACACA	4067
rs550541576	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55939348	TTATCCATGACAATG[A/G]TGGAAAGAAATTAAG	4067
rs550559544	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55934099	GGCATGGTGGCGAGC[A/G]CCTGTAGTCCCAGCT	4067
rs550564105	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55905482	TGAATTAAGGTGGCC[C/T]AGTTAATATCCAGTC	4067
rs550581623	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55899703	TACCCAGGCTGGAGT[A/G]CAATGGCACGATCTC	4067
rs550660534	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55992710	GTGCTCTGCTTCTCA[A/G]ACTCTAAGCTCTGGA	4067
rs550696523	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55906644	TTACAGGCGTGAGCC[A/G]TCACGCCTGGCCGAG	4067
rs550697277	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55993190	ATTCAGTAATTCTTC[C/T]TGGAGGAATAATAAT	4067
rs550698610	snp	A/C	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55985981	AGACCCGCCTGGGCA[A/C]TATAGTGAGACCTCA	4067
rs550722452	in-del	-/C			intron-variant	LYN	GRCh38.p7	8:55995161	AGCTATCCTGAACTT[-/C]CTGACGCCCTCACCA	4067
rs550725166	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55967196	TCAAATGAATTACTA[A/T]GTATTTCAAAAAGGA	4067
rs550750694	snp	C/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55938293	AGAGTTGTATTTGCA[C/T]GTCAAAGCCTCAGTT	4067
rs550754253	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55901391	TGATGGTATTTTTAC[A/G]TTGACTTTAATATGA	4067
rs550762102	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55945138	GATGCAAATTCAACA[A/G]CATTCTAGAAAAAGC	4067
rs550814619	snp	A/G	0.00199481	0.0315187	utr-variant-5-prime	LYN	GRCh38.p7	8:55877350	CAATCCTCCCACCTC[A/G]GCCTCCCAAAGTGCT	4067
rs550818107	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55932964	CGGGAGACTACTAAA[C/G]TGGGGGAGGGAGAAG	4067
rs550861582	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55919532	TGGGCCACAGGCTGG[C/G]GTTTGAAGAAAGAAT	4067
rs550877651	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55903137	CATGCGTGAGCCACT[A/G]CGCCCGGCCTACGCC	4067
rs550888884	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55980966	GCCCCTGGCCACCCC[C/T]GTGCTGTTCTCGGTC	4067
rs550892829	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55989183	GAAGCCGGTTTCACC[A/G]TGTGGGATGCTGGGG	4067
rs550927819	snp	A/C	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55950312	GCTGGGTCCTGTGGT[A/C]AGTCTATGTTTTCTT	4067
rs550941049	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55944648	ACCATGCCTGGCTAA[C/T]TTTTGTATTTTTAGT	4067
rs550944681	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	LYN	GRCh38.p7	8:56012459	CTAGACACAGTGGCT[C/T]ATGCCTGTAATCTCA	4067
rs550951557	snp	A/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55958271	CCTGCACACAGCTTA[A/T]TTTTAGAGAACTTTT	4067
rs550972902	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55893813	TGTTTTTTTTTAGAA[A/G]CAAGATCTCACTATG	4067
rs551018256	snp	A/G	1.64817e-05	0.00287064	missense	LYN	GRCh38.p7	8:55966826	CCCTGCAGCATGACA[A/G]GCTCGTGAGGCTCTA	4067
rs551028580	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56005185	CATAGGCAACCAGTG[C/T]TCTCAGTCTCTACTT	4067
rs551042572	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55937198	CTTTTACCTCACAAG[C/T]GGACTTTAGAACCTA	4067
rs551081723	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55966085	AGCCAAGATCGTGCC[A/C]CTACACTCCAGCCTG	4067
rs551104634	snp	A/C/G			intron-variant	LYN	GRCh38.p7	8:55942854	AAGGAAATGTGGGAT[A/C/G]CAAGTCAGAAACTAA	4067
rs551146372	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55972577	CCACTGCTACCCAGT[C/G]CTCCTCCTCCTCCTT	4067
rs551161375	snp	G/T			intron-variant	LYN	GRCh38.p7	8:56003594	ATCGCTTGAATGCTT[G/T]AACCCAGGAGACAGA	4067
rs551169867	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55966188	CGTTTTTTTGCTACT[A/G]TTTCATAGAAACCTT	4067
rs551177242	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55880598	GCAGTGGGAGATGGG[G/T]CTCGGCCGGCGCCCT	4067
rs551196171	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55969388	CTTCCAGTGAGCTCG[A/C]TAAAGATTGGGAGGT	4067
rs551216093	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55881560	AATTTCACTGGATCA[C/T]AGAGTCTTTGGTGAC	4067
rs551236875	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55998751	AATTAAGCAATGCAA[A/G]ACACAAATAGATTCA	4067
rs551244415	snp	C/T	0.00438332	0.0466095	intron-variant	LYN	GRCh38.p7	8:55942508	ATAGTAGTGAGAGGC[C/T]GGGCGCGGTGGCTCA	4067
rs551253106	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55882259	GTTACAAAGGTAGGT[C/T]GAAACTTTGTAATCC	4067
rs551281286	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55946821	TCTAGGTACCTCCTA[A/G]AAGTGGAATCATACA	4067
rs551286447	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55959157	TTTTTGTTGTTGGCT[C/G]GTTGGCTTTTGTGAT	4067
rs551301618	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55979475	AAACACAGCATTCTT[C/T]GCCTACCCTCGGAGC	4067
rs551304544	snp	A/C	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55900524	ACTTCAGAGTCACAT[A/C]ACCATGCCCAGCTAA	4067
rs551337238	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55939192	GAGGACCTCTGTTGA[A/G]GTTTCTGGTGGGAGA	4067
rs551359416	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55911641	TGTACTAGGGTGTCC[C/T]GTATTTTATCTGGTA	4067
rs551374322	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55921659	GGCAGGTGATGCCAC[A/C]GTGCCAATTAGGAGT	4067
rs551395846	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55881487	GAAAGGGTGGGATCC[A/G]GTTAGTCCCTCCATT	4067
rs551424078	snp	A/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55936885	CCTGAGACCTTTGAT[A/T]ACCTAGCACAGGTTC	4067
rs551451903	snp	C/T	0.00279162	0.0372561	intron-variant	LYN	GRCh38.p7	8:55997895	CGAGACCATCCTGGC[C/T]AACATGGTGAAACCC	4067
rs551483810	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55937483	ACTTAAAGAACTAAC[C/T]CCTAATGAGGACATC	4067
rs551488631	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55972023	CTGGGGGCAATCAAG[A/G]TCGGCACCAGTGGTC	4067
rs551501315	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55992170	TTTGTTCACCCCTGG[A/G]CCTGACATTATAATG	4067
rs551509394	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55900004	GTCATGTCACTGTAC[A/G]AGGTGGAGCTGAACT	4067
rs551542908	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55905404	ACAAGAGTGAAACTC[C/T]GTCTCAAAAAAAAAG	4067
rs551607184	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55906568	CACCATGTTGCCCAG[A/G]CTAGTCTTGAACTCC	4067
rs551618817	snp	C/T	0.00438332	0.0466095	intron-variant	LYN	GRCh38.p7	8:55934195	TGTGCCATTGCACTC[C/T]AGCCTGGGCGACAGA	4067
rs551653938	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55883786	ACTGTTCTAGGCCAA[C/G]AGTATAGATATACAT	4067
rs551709415	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55902001	CATCATTCTAAAAAA[C/T]GTACCTGTACTTTCT	4067
rs551761449	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55903295	ACCGTGCTGGGCCTT[C/G]TACTTTCTTGAATGG	4067
rs551789554	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55925899	CACCACAGAAGCATA[C/G]AAGTGTTTATGTAAA	4067
rs551806521	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55948116	GAAGCTAGGACTACA[A/G]GCATGTGCCACCAGG	4067
rs551817044	snp	C/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55934734	CCTGTGTTGAGGGGG[C/G]TGCACCCTGTAACTA	4067
rs551834159	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55964906	GCACCCTAAAAAGGG[C/G]ACCGTCCACTCCACG	4067
rs551852674	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55987326	GGCACAAGAATTGCT[C/T]GAGCCCCGGAGGTGG	4067
rs551866434	snp	A/T	0.00597247	0.0543191	intron-variant	LYN	GRCh38.p7	8:55948245	TCCCAAAGTGCTGGG[A/T]TTACAGGTGTGAGCC	4067
rs551877785	snp	G/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55928307	AGCGCCACCACGCCC[G/T]GCTAGTTTTTGTATT	4067
rs551958116	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55977735	CTGGGCAACACAGTG[A/T]GACTCCTATCTCTAC	4067
rs552015820	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55890267	CAGTGAGCAATGATT[A/G]CACCACCACACTCCA	4067
rs552038863	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55925103	GTTGGGATTACAGGC[A/G]TGAGCCACCGTGCCC	4067
rs552051334	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55918522	ATGTGCAGCAAAATA[C/T]ATGTTTAAGTGAATC	4067
rs552084539	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime	LYN	GRCh38.p7	8:55877778	GTCAAGGAGCCTTAA[C/T]TGATTTGCACCCTGC	4067
rs552101204	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime	LYN	GRCh38.p7	8:56010850	CCTGGACCTCCCAGG[A/T]AAGGGAGAAGAGCCT	4067
rs552108237	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55979914	CTCCTGCCATAGTTG[C/T]TGCCTCCTGGCCTCT	4067
rs552139906	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime	LYN	GRCh38.p7	8:56011687	GATGGGATAAAATAT[A/T]CTACTTTTTTCTAAA	4067
rs552140006	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:56003870	ATTAATTTTCTTCTT[A/G]ATGAATTTCTGAAAT	4067
rs552143226	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55888770	GAGACAGAGTCTCAC[C/T]CTGTCATCCAGGCTG	4067
rs552155550	snp	A/G	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55889164	AGGATTACAGGCCCC[A/G]CCACCAGGCCTGCGT	4067
rs552197751	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55915479	GGAAGCCAAGGCAGG[C/T]GGATCACCTGAGGTC	4067
rs552227308	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55987910	TTAACGACTAACATG[C/G]CTAGCACAGTGCCTG	4067
rs552279198	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55981191	ACACCACACCTCTTA[G/T]CAACAGGCACCTTCC	4067
rs552288071	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56005828	GTAGCTCATGCCTGT[A/G]ATCCCAGCACTTTGG	4067
rs552295148	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55886803	AATTTAATACATCAT[A/G]TAATTTGTAAAGATT	4067
rs552306248	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55973967	ATCAGAGTTGTTGTA[A/G]TTATCATGGCAACAA	4067
rs552341864	snp	C/T	0.00398564	0.0444627	intron-variant	LYN	GRCh38.p7	8:55981645	ATAGGTGTGAGCCAC[C/T]GTGCCCGGCCAGAAC	4067
rs552352066	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55975201	TGCTTGGAAACCTCA[A/G]CTTTCTCAGTATACA	4067
rs552376127	snp	G/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:56006783	TCACCAGCTAATGGG[G/T]GTTTACTTTCTTTAA	4067
rs552384594	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55883860	AAGAGGAAGTTGTTG[A/G]GTTTTTTTTTTCCAG	4067
rs552392072	snp	C/G	0.00716266	0.059414	intron-variant	LYN	GRCh38.p7	8:55920935	CTCCTGACCTCAGGT[C/G]ATCTGCCCGCCTTAG	4067
rs552415201	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56000369	AGATTCCTAACACCT[C/G]AAGCCTGCAGAGCCA	4067
rs552420092	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55929028	ATATACAGTTGTTCC[A/G]GTACCACTTATTGAA	4067
rs552420837	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55967579	CCTCAGCCTCTGAAA[A/G]TGCTAGGATTACAGG	4067
rs552453293	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56007838	AAAATACTGGTAATT[G/T]GCTGGATGCAGTGGC	4067
rs552459248	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	LYN	GRCh38.p7	8:55877056	ATTATGATTAATACA[A/T]AACCTTATATGGTGT	4067
rs552459914	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55913704	TCTACTTGAAATAAG[A/C]ACAGACGTGGAAGAA	4067
rs552466072	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55977254	AGACTAAACTGTTTT[A/G]TAGATAACTCTGGTT	4067
rs552544809	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56008319	AGCTGCCACTTATTT[A/G]GAATCCTTCCAGTGA	4067
rs552551333	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	LYN	GRCh38.p7	8:56012668	AGGCTGCAGTGAGCT[A/G]TGATCGTGCCACTGC	4067
rs552597560	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55939468	TCCCAAGAGAAGAGA[C/G]AGAGAGAGAGAGAGA	4067
rs552617192	in-del	-/TT			intron-variant	LYN	GRCh38.p7	8:55998116	GTTAAGACATGTTCC[-/TT]TTTTTTTTTTTTTAA	4067
rs552629521	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55934046	GCCTGGCCAATATGG[A/T]GAAACCCCATCTTTA	4067
rs552629696	snp	C/T	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:55926897	GCTCCTTGTGGAGCC[C/T]GGCTAACTCCTAGGC	4067
rs552630162	snp	G/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55920407	GTGATCATGTCACTA[G/T]AACCTGGCTTTCCTT	4067
rs552640189	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55885679	CCCACGGAGGTGAGG[A/G]GAATGGAGAAGCTTA	4067
rs552685248	in-del	-/ACCA			intron-variant	LYN	GRCh38.p7	8:55956243	TCACCAGTTGTTAAT[-/ACCA]ATTGTCCTAATTTTC	4067
rs552693009	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55927460	GTGTTCTGTTGTCTG[A/G]ATATAAAATGGATAA	4067
rs552700617	snp	C/T			intron-variant	LYN	GRCh38.p7	8:56004329	GACAGAGTCTCGCTC[C/T]GTCACCCAGGCTAGA	4067
rs552745755	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55933875	CCCTTCACATTGTGG[A/G]TAACTAGATGACCCT	4067
rs552764795	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55960316	GCATTGATCACCGTT[C/T]ATTTTTTAATTGTGC	4067
rs552793048	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55960697	GATAGAAAAAATACA[A/G]TTAAAATTCTATCAC	4067
rs552805165	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55953728	TAGTTCACAGACTGC[A/G]GCAGGTTGGACACTA	4067
rs552812557	snp	A/G/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55914239	GTCTGGAGGTCGGCC[A/G/T]TGGAGTGGAGAAGAG	4067
rs552812971	snp	C/T	0.00438332	0.0466095	intron-variant	LYN	GRCh38.p7	8:55912930	ACTTTTATATAGTAA[C/T]GAAATTTCATAATTA	4067
rs552835281	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55973622	TGTCAAACTGAGAGG[A/G]AAGAGCAGTGAAAAA	4067
rs552866792	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55954454	TTTCTTAACATTAAG[G/T]ATTGCCTTCTCAGGC	4067
rs552868418	snp	C/T			intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55922835	ATGAGTGTAGCAAAA[C/T]GGGAGGGTGCCAGCT	4067
rs552878661	snp	A/G	0.00279162	0.0372561	intron-variant	LYN	GRCh38.p7	8:55882767	TTGTGGCTCCTATAG[A/G]ATGGAGAGGGACAGA	4067
rs552884065	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55960854	CTTTGGGGGAAGGGG[A/C]TGGGTGGGGATAAAA	4067
rs552885742	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55900844	AGAATAGCTCTTGGA[A/C]ATCTTATATTCTCCT	4067
rs552901878	in-del	-/CTT	0.00716266	0.059414	intron-variant	LYN	GRCh38.p7	8:56006513	TACCACATTTTTCTC[-/CTT]CTTCTGCTTCTTTAC	4067
rs552901911	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55979111	CCACGGTGGAGTGCA[A/G]TGGTGCTCACTGCAA	4067
rs552914157	snp	C/T	0.00318978	0.0398085	intron-variant	LYN	GRCh38.p7	8:55986123	GCAGTGAGCTGTGAT[C/T]CTGCCACTGCTCTCT	4067
rs552918313	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55947029	AAGTTAGGTAGATCA[C/G]CTGTGGTCAGGAGTT	4067
rs552940178	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56004365	GTGGTGTGATATCGG[C/T]TCACTGCAACCTCCA	4067
rs552954693	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55894720	TTGTATTTTTAGTAG[A/G]GACGGGGTTTTGCCG	4067
rs552957480	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime	LYN	GRCh38.p7	8:56011196	GATATGAAGGAACAT[A/G]AGTGACTACAAGGCT	4067
rs553018043	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55895360	AAATAACTTGGCTGG[A/G]TTCCTTACTAATCTT	4067
rs553043558	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55918797	GGGCCAGCCAACTAC[A/C]CGGGGATTCTGATCG	4067
rs553055937	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55919638	AGAAAAACCCATGCC[C/T]GTGGGAACAAGTAAC	4067
rs553087041	snp	A/G			intron-variant	LYN	GRCh38.p7	8:56000964	TAGTGGGGAGAGACT[A/G]ATGTTTATCAAACAC	4067
rs553117063	snp	C/T	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55949037	CAGCTTACCTGCTTG[C/T]TTCTTCCAGTGCTCA	4067
rs553121580	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55925400	AGTGCTGGGATTACA[A/G]GTCCGAGCCACTGCG	4067
rs553130162	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55888940	TTTCAGAACCACACT[A/G]GCTTTTTGTATTATT	4067
rs553155724	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55950612	CCACATTGGATTTCT[G/T]GTTAATATTCTTCAC	4067
rs553177567	snp	A/C	0.000399281	0.0141238	downstream-variant-500B	LYN	GRCh38.p7	8:56012810	GTTTGACCCATATTA[A/C]AAAGCCCAGCCTTCT	4067
rs553224906	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55921106	TAGATACGTCTGAAA[C/T]GAAAACAATTTTGGG	4067
rs553273720	in-del	-/T			intron-variant	LYN	GRCh38.p7	8:55920679	CTTTACTTCAGGAAA[-/T]TTTTTTTTTGAGACA	4067
rs553274161	in-del	-/GT			intron-variant	LYN	GRCh38.p7	8:55914099	GGAGGGTTGTTGTTG[-/GT]GTGTGTGTGTGTGTG	4067
rs553289284	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55959266	ATCTTTTCATGTCCT[C/T]CCTGGTCATTTCTAC	4067
rs553291965	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55913281	TTTCCAAAGGTATTC[A/G]GATTTTAGTAGGGGA	4067
rs553294534	snp	A/C	0.000399281	0.0141238	utr-variant-5-prime, missense	LYN	GRCh38.p7	8:55879827	CTCGGCCGAGCCCAG[A/C]GACAGCCAGTTCCTC	4067
rs553303458	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55952427	TAGCCAGGCATAGTG[A/G]TGCGTGCCTGTAGTC	4067
rs553310087	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55913899	GCTTTCTTATGGCTG[C/T]GAGAGAGGATGAGTT	4067
rs553337961	snp	C/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55884467	TTTTTATTCTGCCTC[C/G]CACTGAAGAGACAGA	4067
rs553362584	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56007975	AATACAAAAATTAGC[C/T]GGGCATGGTAGTGGG	4067
rs553424193	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55965590	AAAATTAAAATCGCT[C/G]GTAATCACACCATTG	4067
rs553427045	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56004160	TGATCTTGAACTCCC[A/G]ACCTCAGGTGATCTG	4067
rs553519600	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55909896	AGGATTTTTTTCATA[C/T]GCTTGCTGGCTATTT	4067
rs553529422	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55951778	TGGCAAGCTACACAG[A/C]AAACAAAATGCCAGC	4067
rs553535735	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55925755	GAGGACACCCTGGAC[A/G]CTGGTGACTGGTATA	4067
rs553538418	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55966226	TTGAATAATTTAAAC[A/C]TTTTTTGGTAAAGAA	4067
rs553620820	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55995108	CACCAAAATTGCCAC[A/C]CCGTGTCATCTGTTT	4067
rs553638425	snp	G/T			intron-variant	LYN	GRCh38.p7	8:56002548	TAGAGGTTGCAGTGA[G/T]CCAAGATTGCACCAC	4067
rs553652164	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55944316	GATATAGAACCATAT[C/T]ATATATAAATATGAT	4067
rs553654540	snp	A/G	0.00438332	0.0466095	intron-variant	LYN	GRCh38.p7	8:55902885	ACGGAGTCTCTCTTT[A/G]TTGCCCAGGCTGGAG	4067
rs553660374	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55992252	CCAAAAGATTTTATC[A/G]GTTTCCCAAGCTCTG	4067
rs553673094	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55949248	GACTCTCATTTCTAT[A/G]AGGATTTGAAAGCAT	4067
rs553682426	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55969807	AGGTAACATATTCAA[A/G]AAGCCCCGTGTGCAC	4067
rs553748110	snp	C/T	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55992771	AGATACAGTGCCTGG[C/T]GAGGTACTTCTTTCT	4067
rs553768664	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55955351	AATTACATGACTTCA[C/T]ATTCTCCGTGTGGAT	4067
rs553817600	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55962677	GTTTTCAAGATATAC[A/G]ATCATTTATCCATTT	4067
rs553840932	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55986926	GATAGGGTCTTGTTA[C/T]GTTGTCCAGGGTGTT	4067
rs553853344	snp	C/T	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:55987575	GTGCCCGCCACCACA[C/T]CTAGCTAAGTTTTGT	4067
rs553861908	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55978107	TAAACCTCTCAACCA[A/G]GTGGCTTTCCTGGTG	4067
rs553899683	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55993673	ACATGAATTGAGTGT[A/G]AAGGATGTGAAGCAG	4067
rs553914133	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55981275	TCAGTCTCGGTCCCC[A/G]CCCATTTCTTCCATA	4067
rs553934711	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55949779	TTATTGAGAATTCAC[A/G]ATACCATACAATCCA	4067
rs553938233	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55953538	CTGTAATCCCAGTTA[C/T]TTTGGAGGCTGAGGC	4067
rs553940643	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55926835	CTTTTAAAAAAATTA[A/G]TAGACTTTATTTTTT	4067
rs553998423	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55943093	TTTCGGAAATACTTG[A/G]CAAAGAAAGAACTAA	4067
rs554014760	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55903165	GCCCAGCTAATTTTT[A/T]TATATTTGGTAGAGA	4067
rs554042417	in-del	-/TTACGCAGTAAAC	0.00716266	0.059414	intron-variant	LYN	GRCh38.p7	8:56003026	CTGAAAGTACTTTCT[-/TTACGCAGTAAAC]TGCTGGCTATGTTTT	4067
rs554068524	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55989250	GAAAGATGAATGACC[C/T]GGATGGTCATCACTA	4067
rs554069705	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55890945	TGTTGTCCAGGCTAA[C/T]CTTGAACTCCTGGGC	4067
rs554078834	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55956602	TAAATAGAACTTTCT[C/T]CAAATGGTTTCAGCA	4067
rs554120320	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55928438	GTCATGAGCCACCAC[A/G]CAGGGCCCATTGTTG	4067
rs554156209	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55989928	GGGGAGGCTTCCAGG[A/C]CATAAGTGGATTCAA	4067
rs554172043	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55921209	GAATTGCTGCTGACC[A/G]CAAACTATGGAATAA	4067
rs554183636	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55922422	GCCTGGTTCTATGTG[C/T]GCCAGTGTATTAATT	4067
rs554189452	snp	A/G	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55894174	TGTCTGCATCCCCCA[A/G]CCCCCCCAGCTTATT	4067
rs554196770	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55994457	TGAGAATCATTTTTT[A/T]AAATGCACTCAGATT	4067
rs554235313	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55922377	TTATAGGCATGAGCC[A/G]CCACACCTGGCTGAC	4067
rs554265642	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55923089	AGTGACAGGATGACT[A/G]AGGGTTTGAGCCTCG	4067
rs554278713	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55902124	GCAATTCTCCCACCT[C/T]AGCCTCCCGAGTAGC	4067
rs554283094	snp	A/G	0.00557542	0.0525036	intron-variant	LYN	GRCh38.p7	8:55940521	GCTGGGACTACAGGC[A/G]TGTGCCACCACGCCC	4067
rs554283374	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55907880	CACATAAATAAGTAA[A/G]TAGTTTAAATAAATA	4067
rs554294885	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55896386	GGAAACCATCATTCT[C/T]AGCAAACTAACATAA	4067
rs554351561	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55948725	TGTTGCATATGGGTT[A/G]AACAGGGACTTAAGC	4067
rs554378111	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55915574	AGCTGGGCATGGTGG[C/T]GGATGCCTGTAATCC	4067
rs554397963	snp	C/T	0.00716266	0.059414	intron-variant	LYN	GRCh38.p7	8:56000896	AGTATGCTAGGCACT[C/T]TCAGCTGCTAGGATG	4067
rs554404482	snp	C/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55961930	CTATTCCGACCTTCC[C/T]GATGGTTTTCTGACT	4067
rs554482127	snp	A/G	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:55887291	TCAAACAAACAAACA[A/G]TAGCAAAAGAGCTGA	4067
rs554508619	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55976848	ATGCAAGTGGGGGTA[C/T]ATGGAGAGAACAGCT	4067
rs554561269	snp	G/T	0.00159617	0.0282053	intron-variant, downstream-variant-500B	LYN	GRCh38.p7	8:55968272	TATATATTTATTTTT[G/T]TGAGACAGAGTCTCA	4067
rs554594729	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55892283	AAAATAGCCAGGTGT[A/G]GTGGCACACACCTGT	4067
rs554597077	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55999801	ACATGGAGAAACCCC[A/G]TCTCTACTAAAATTA	4067
rs554609000	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55972753	CCCACGGTGACAGAG[A/T]TCCCTGGGGCCCAGA	4067
rs554623117	snp	C/G			intron-variant	LYN	GRCh38.p7	8:56006856	GTCTGGTTGAGGTCC[C/G]TCTCCTCTTCTTATT	4067
rs554624467	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55969122	CCTATCTCTACAAAA[A/C]AAAGAATTAGCTGGG	4067
rs554677351	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56007906	GGCAGACGACTTCAG[A/G]TCAGGAGTTTGAGAC	4067
rs554696658	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55999740	ACTTTGGGAGGCCGA[A/G]GCAGGTGGATCACCT	4067
rs554698311	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55913190	GGCCCCTCTGTTAAA[A/G]TCTTTTAGCAAAAAG	4067
rs554715461	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55895525	CTGGGTGTGGTGGCT[C/T]ACACCTGTAGTCACA	4067
rs554726370	snp	A/G	0.00279162	0.0372561	intron-variant	LYN	GRCh38.p7	8:55943736	AAATATCTGCCATGT[A/G]TCAAAGTCACATGTC	4067
rs554741772	snp	C/T	3.29462e-05	0.00405857	synonymous-codon	LYN	GRCh38.p7	8:55969734	AGTTTGCTGGATTTC[C/T]TGAAGAGCGATGAAG	4067
rs554744393	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55962575	TCATTCATCTTCATT[A/C]CATATGGTATTGGTG	4067
rs554745407	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	LYN	GRCh38.p7	8:55876669	CTACTTGGTAGTTAG[G/T]TCTGTGGCCAAGTTG	4067
rs554756930	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55955592	GCATTTAGTACATTC[A/G]CAATATTGTGTAGCC	4067
rs554763635	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55906421	ACACCCAGCAATGGC[A/G]TGATTTCGGTTCACT	4067
rs554765242	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56001299	GATCTCTAGACAGTC[A/G]ATGGATGAGAAAGAA	4067
rs554784415	snp	C/T	0.00199481	0.0315187	upstream-variant-2KB	LYN	GRCh38.p7	8:55877184	CTCCAGTGGGCACGC[C/T]ACAGCCTCTGGTGCT	4067
rs554821506	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55994628	TGGCCGATCAACAGC[A/G]TTGGGAGAGGGGCAG	4067
rs554827810	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55895869	TAAACTGTACTACCC[C/T]GAGCCTTTTCTTGAT	4067
rs554835263	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55986886	ATGTGCCACTACACC[C/T]GGCTAATTTTTAATT	4067
rs554846604	snp	C/T	0.0737376	0.17729	intron-variant	LYN	GRCh38.p7	8:55909036	ACACACACACACACA[C/T]ACACACACACACACA	4067
rs554891326	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55896303	AAAAAGAAACAACAA[C/T]ATCAAACAAAGAAAC	4067
rs555000842	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55997590	TGATCTAATCACCTG[C/T]CAAGGCCCTGCCTCC	4067
rs555002158	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55930446	CTGAATCTGGAAACA[A/G]AGTTGATGTTTAATA	4067
rs555019061	snp	A/C	0.230017	0.2492	intron-variant	LYN	GRCh38.p7	8:55953751	GGACACTATAAGGCT[A/C]GTGTTCAACTTTTCT	4067
rs555058129	snp	C/G	0.0154538	0.0865337	intron-variant	LYN	GRCh38.p7	8:55907130	ACAAAAAGACATGTC[C/G]AGTTCTATATATGGC	4067
rs555072958	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55947234	AGTCTGGGCGACAAG[A/G]GCGAGACTCCGTCTC	4067
rs555086205	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55991050	CAAATAGAGACACGC[C/T]GGCAGTACTACCACG	4067
rs555088748	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56003329	GCCTGCCAAAGTGCT[G/T]GGATTACAGGCACGA	4067
rs555094290	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55898815	CTATAATAAATTTTA[A/G]GAAACTGGTTTTAAT	4067
rs555106409	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55956732	ACCCCACTGGCTCAC[A/G]TCAAGATCCAGGGAC	4067
rs555119565	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55933663	GACTGTCAAGGCTGG[A/T]CTCCACAGACAGGCT	4067
rs555143609	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55951067	GGGCAACACAGCAAG[A/T]CCCCATCTCTACAAG	4067
rs555145315	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55958327	TAGGAGAAACAAGTT[C/T]AGAAGAGAAGAGAAT	4067
rs555182929	in-del	-/ATTTATTT			intron-variant	LYN	GRCh38.p7	8:55908255	TTTATTTATTTATTT[-/ATTTATTT]GAGACAGAGTCTCAC	4067
rs555211173	snp	A/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55904338	ATTTCTTAGAATATG[A/T]TATGAAATATGATAT	4067
rs555229069	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55893345	GGGTGGTTTCCACTG[A/G]CCCACATGTAATCAA	4067
rs555230883	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55978727	TGCAGCGCAGGCGAC[A/G]GAGTTCTGACACGCA	4067
rs555246961	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55940293	CCACTGTGCCCCAGA[A/G]GAGTTTCCCGGACAG	4067
rs555265567	snp	A/G			downstream-variant-500B	LYN	GRCh38.p7	8:56012493	CTTTGGGAGGCTAAG[A/G]CAGGAGGATCGCTTG	4067
rs555268088	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55980941	GCCAGCTCCCCGCGG[A/C]CGCTTGCTAGCCCCT	4067
rs555274760	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55935628	AAAATACAAAAATTA[G/T]CCATGCTTGGTGGCG	4067
rs555289358	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55981253	ACTCCTGCTTACTCC[A/T]TTCTCCTCAGTCTCG	4067
rs555325446	snp	A/G	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55942411	TATATATGTGTATAT[A/G]TATGTGTGTATATAT	4067
rs555347007	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55974495	GGGCCTTTTAACAGC[A/G]GAGCTTTCTGAGCAC	4067
rs555417960	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55903851	AGACCCTATCTTTAC[A/G]GAAAATAAAAAGAAA	4067
rs555507559	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55983885	TGGGGCTGTCAGGGC[G/T]CTTAAAACAATAGAA	4067
rs555561562	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55963309	TTTGCAAAGTGCTGG[C/T]CCCAGCTTAAGATTC	4067
rs555561981	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55975545	TGATATAAGATTTTA[A/G]CATTGCTCTAAATAA	4067
rs555591099	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55931751	TGAAGTATCATGTTC[C/T]AGATCAATTTTCCAA	4067
rs555654761	in-del	-/A	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55911555	AGGGGCAGCAGGTGG[-/A]AATGTACATTCACTA	4067
rs555683797	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55886449	GACAGGGTTTCATCA[C/T]GTTGGCCAGCCTGGT	4067
rs555684365	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55885854	GCCCCTGGGTCATTT[G/T]CCTGCAGCCCCACCT	4067
rs555690555	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56008893	CTCCTCAATTAATAT[A/C]TTGCTCTTAAAAGAC	4067
rs555744676	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55971584	TCCATCTGCTGGGGG[A/T]CTGATCTGTACCCAC	4067
rs555754240	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56002203	TGTGGGCGGATCACA[A/G]GGTCAGGAGATCAAG	4067
rs555761220	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55966080	CAGTGAGCCAAGATC[A/G]TGCCACTACACTCCA	4067
rs555771978	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55886433	TTGTATTTTTAGTAG[A/T]GACAGGGTTTCATCA	4067
rs555777590	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55989199	TGTGGGATGCTGGGG[C/T]TGACAGACTTCTCAC	4067
rs555786069	snp	C/T	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:55935735	GCAGTGAGCCGAGAT[C/T]GCACCACTGCACTCC	4067
rs555791303	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55996205	ATGGTTTTTGTACAC[A/G]TTGACCATCTAGGGT	4067
rs555845973	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55929926	TGTGGCCTGTTAGGA[A/G]CTGGGCCACACAGCA	4067
rs555848330	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55903213	GGCCAGGCTGGTCTC[A/G]AACTCCTCACCTCAA	4067
rs555880885	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55996947	CCAGCCTGATGAAAC[C/T]CCATCTCTACTAAAA	4067
rs555885552	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55897437	TGCACATGGTGGTTT[C/T]GAGGGGTTGACAGCA	4067
rs555891565	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55986395	TACAGTGAGTTTTGA[A/C]ATATCTATCCCAAAG	4067
rs555892879	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55885347	CTCATTTCCTTTCTA[C/T]AGTCCATGCTTCAGG	4067
rs555922517	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55989488	CATGAGGGAGAGCCC[A/G]GTTGCCTTTCCTCGA	4067
rs555929796	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55878060	TTGCACACCATACAT[A/G]CTACAGATGCTTTAA	4067
rs555984379	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55955473	TGTTGTCTCTTCCCA[C/T]GCACACTCTGTTGTC	4067
rs556024100	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55898167	GCCACCCCCAGCCCA[A/G]TGCCTGGCAACTGCT	4067
rs556025159	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55989347	CTCTCTATCAAACCC[A/G]CATAAAAGAAGTCCA	4067
rs556045841	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55978407	CCGCCATTGCGGGCA[C/T]GGGGTTGAGGTGGCT	4067
rs556058483	snp	A/G			intron-variant	LYN	GRCh38.p7	8:56005876	ATTGCTTGAGGCCAG[A/G]AATTTGAGACCAGCC	4067
rs556059032	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56002882	TAAACATAATCAAGC[A/C]ATCCTATTTACTTCA	4067
rs556076489	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55943226	TGTATACATGTATAC[C/T]ACCCATAGCCTGCTT	4067
rs556077365	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55963216	CAAGCATGCATGAGC[G/T]CTAGGGTGAGTGGGA	4067
rs556088233	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55924394	TTGAGATGGAGTCTT[A/G]CTCTATGATCCAGGC	4067
rs556098422	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55917175	AGTGAGATTCTGTCT[A/G]AAAAAAAAAAAAAAG	4067
rs556142418	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55949141	TGGAATTGTCTTATG[A/G]TTTTCTTCTTTTCAT	4067
rs556161162	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55916209	AAAATGGTGGTATTT[G/T]ATTGGTTTTAAAGAG	4067
rs556168007	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55935564	GTATCACCTGAGATC[A/G]GGAGTTGGAGACCAG	4067
rs556210773	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55956549	TTTTTACTCCCTTTT[A/G]TAGTAAATAAATACT	4067
rs556218276	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55910017	TTTTTTTTTGAGTTG[C/T]TTGAGTTTCTTGTAA	4067
rs556300557	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55990117	GGTGGCGGACACCTG[C/T]AGTCCCAGCTACTCA	4067
rs556316375	in-del	-/G	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55979863	TCCGGGGCTGCCAGA[-/G]GGCCGCCCACCCTGG	4067
rs556322753	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55949819	AGTGTACAATTCAGT[A/G]ATTTTTTTAGTATAG	4067
rs556322836	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55957126	TATTTGCTACACTAT[A/T]TCTAAGCTAATTTGA	4067
rs556354131	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55935026	GCCCACACCATGGAC[A/G]GAAGCAGCTCCACGG	4067
rs556364493	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55896493	GGAACATCACACACC[A/G]GGGCCTGTCGGGGGG	4067
rs556383645	snp	A/G	1.64792e-05	0.00287042	missense	LYN	GRCh38.p7	8:55950547	AAACTCAACACCTTA[A/G]AAACAGAAGAGTGAG	4067
rs556390631	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55936437	CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC	4067
rs556408794	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55983162	GAGCCTCATGAACCC[C/T]GACATGTGCCCAGTC	4067
rs556427773	snp	A/T	0.00398564	0.0444627	intron-variant	LYN	GRCh38.p7	8:55890569	CATATGATGCAGCAA[A/T]GCTGCTTCTGGGTAT	4067
rs556468026	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55892499	TACAGTTATATTAAT[A/G]TTTCTAGCCATGCAC	4067
rs556471229	snp	A/G	0.00676609	0.0577691	intron-variant	LYN	GRCh38.p7	8:55887331	AGTAGATGACATGAT[A/G]CCATTTCTGAAATAA	4067
rs556544810	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55977029	GTCTCTACTAAAAAT[A/C]CAAAAGTTAGCCGGG	4067
rs556572064	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:56008128	TGCCTCAAAAAAAAA[A/G]TAAAATAAAATAAAA	4067
rs556573450	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55918968	CTTTGGGAGTTCGAG[A/G]CAGGAGAATTGCATG	4067
rs556584500	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55988520	GCTTTTGAACATCAT[A/T]AATTATGTGAATTCT	4067
rs556621134	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55978242	ACCTGTGCTTTAAAA[G/T]TTGCCCCAGCCACCG	4067
rs556661179	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55881956	CTATGCAAAACTGAG[A/G]ACATAGGGAGATGAA	4067
rs556662457	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55896893	TACAGGTGCCCGCCA[C/T]CACCCCCAGCTAATT	4067
rs556674725	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55891019	CAGGCATGAACCACC[A/G]TGCCCAGCCATACAA	4067
rs556677368	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55902616	TACAAAAAAAAAACA[A/G]CAACAACAGTAGTCC	4067
rs556677437	snp	A/G			utr-variant-3-prime	LYN	GRCh38.p7	8:56011680	CTTAGAAGATGGGAT[A/G]AAATATTCTACTTTT	4067
rs556700479	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55972905	AGTTAGTAGGCTGTG[C/T]GATAATGATGCGACT	4067
rs556701391	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55935363	GCTGGGAGATTTTAT[C/T]GAGGAAAAATATTGG	4067
rs556718057	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55982980	TCCTCCCCTAGCTTG[A/G]AGACACTCATTGCCC	4067
rs556741423	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55881943	CTGTGAGCTTGCCCT[A/G]TGCAAAACTGAGGAC	4067
rs556747954	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55920474	CATTGTTTACTTGCT[C/G]TGAGAGAGCATTTAA	4067
rs556837261	snp	A/G	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:55888135	TATGTTTAGTATTCA[A/G]TTTAGCAAACTTTTC	4067
rs556840969	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55929158	TGTACTGAGTCTTTT[C/T]GTTACTTTCAGTGAA	4067
rs556842091	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56008705	TCTCTATTACCAGGC[C/G]TTTTGCAGAGCTCTA	4067
rs556851290	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55943122	AACATCACATTTTAT[A/G]GAAAGGAAGAACAGA	4067
rs556854754	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55970387	GCAGAAGCAAGTTAT[C/T]CAGAAGCCCCACAAT	4067
rs556856965	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55929839	TATTTATATCCATGG[A/T]TATGTTTTCCTCTTT	4067
rs556859659	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55933255	TGAAATAATTAAAAG[A/T]TACCAATTTTGGTGA	4067
rs556874248	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55967242	ATGCTTAAAATGTGA[A/G]GAGTTCCCAGAATTC	4067
rs556887396	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55984672	CTCCTGTGCTCAGCT[A/G]TGGCTTCCCCCAGCC	4067
rs556942943	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55914499	CACTATGCAGTGAAT[C/T]AAGCCAGGTCAGCTG	4067
rs556960878	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55937959	GCCTCGGCCTCCCAA[A/C]GTTCTGGGATTACAC	4067
rs556980521	snp	C/T	0.00358779	0.0422022	intron-variant	LYN	GRCh38.p7	8:55924523	GTCCACCCACCATGC[C/T]CGGCTTATTTTTGTA	4067
rs556980946	snp	A/C	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55931670	TTAAATATATTGTGA[A/C]TATCTTTTTATGTCA	4067
rs556987849	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55932689	GCCTCCCAAAGTGCT[A/G]GGATTACAGGCATGA	4067
rs557002873	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56005379	GCATTCCCTGCATGA[A/G]GCTTCTCCATTGTTT	4067
rs557029536	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55893255	ATTAGTAAAATTAGC[C/T]GGCATAAGCTATATA	4067
rs557065881	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55887687	TGATCTCGGCTCACT[A/G]CAACCTCCACCTCCC	4067
rs557096436	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55886396	AGGCATGCACCAATG[C/T]ACCACCATGCCCGGC	4067
rs557139826	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55888829	GGGATTTGGCCACCA[C/T]GCCTGGCCGAATCCC	4067
rs557237006	snp	A/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55926458	TTAACTGTGCATTTC[A/T]TTTATCATAAATGGC	4067
rs557243766	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55912523	TGAGGTCCAGGAGTT[C/T]GAGACCAGCCTGGCC	4067
rs557251092	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55919853	CTCTCCAGGCAAAGA[C/T]GCTGCTTGGAGGCAA	4067
rs557254381	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55959448	ACAATTGAAAGAAAT[C/T]GTGCAGGTAAGTTCA	4067
rs557304564	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55918684	TTACTATGGCCTTGC[C/G]GGGTAGGGGGCAGTG	4067
rs557314369	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55920553	TTATCTACCCTTCAC[A/G]GATGAGGAAAATGAA	4067
rs557355088	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55977399	TTTGTATTTACTGTA[A/G]TATGTATTCATGTTA	4067
rs557364567	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55911834	TTGGTTTTAAACTTC[A/G]GCACCTGGTGCCCTT	4067
rs557419778	snp	C/T	0.0023933	0.0345097	utr-variant-3-prime	LYN	GRCh38.p7	8:56010488	ATGAATCCCCAATAA[C/T]TGCAGAACTAAACTC	4067
rs557420552	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55984039	CATTCCATGTCTTGT[G/T]GACCGCACTGCTCCT	4067
rs557451794	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55900096	CGAACTTCAGGAAGA[C/G]AAGAGCTCAGACACT	4067
rs557464614	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55964812	TCACTCCAAATTCTA[A/C]CAGCCAGGGATAATC	4067
rs557470510	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55951621	AGTTAGCTATGATTG[C/T]GCCACTCTACTCTAG	4067
rs557489398	snp	C/T			intron-variant, utr-variant-3-prime	LYN	GRCh38.p7	8:55967909	AGTAATGAAGAAACA[C/T]AAGCAATGATCCAGG	4067
rs557526206	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55957812	ATTAGTTGAGCATGG[C/T]GGTGTTGCACCTGTG	4067
rs557526674	in-del	-/T			intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55923547	TTTAGGTCAAACAAC[-/T]TTTTTTTTTTGAGAC	4067
rs557531629	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55945469	AGTAATTTTCCCTGT[C/T]TCACTGAAATGGAGA	4067
rs557548840	snp	A/G	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55887492	GAATGAGCATCCCAT[A/G]TATACATAAATATAT	4067
rs557564317	snp	C/T	0.00279162	0.0372561	intron-variant	LYN	GRCh38.p7	8:55911325	CAGGGTTTCACCATG[C/T]TGGTCAGGCTGCTCT	4067
rs557603862	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55997732	TGGCATAATAACATC[C/T]ATGTATCTACATGGA	4067
rs557608130	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55978890	AACCCTGTTCTCTGC[C/T]TGCACAGGCTCCTCC	4067
rs557610959	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55899383	TAACTTTGAAAGGTT[A/G]TTTTTTAAAAAATCA	4067
rs557621178	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55893913	CTGGGCTGAAGTGAT[C/T]CTCCTGCCTCAGCTT	4067
rs557659360	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55887982	CTGCAGAAGGCAGGT[A/G]GAAGCAGACAGGGAA	4067
rs557663428	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55959338	TTTTAAATTGTGTTC[A/T]TTACTTGATTTACTA	4067
rs557675797	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55880858	TGCATTCTCTGGGCC[C/T]ATGGTGGCATCTTTT	4067
rs557676752	snp	G/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55991688	TTCTTTGTCATCAGC[G/T]TCAGGCACAGGCGTT	4067
rs557685518	snp	C/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55904579	TTACCCTGCAGATCA[C/T]GCACCTATAAAAGAT	4067
rs557699581	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55904955	TGGGGAGCATTTAAA[C/T]CTCCCCATGCCCAAG	4067
rs557718423	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55935851	TGAGTTGGGAATTAA[C/T]GGAGTTGGTGGTGGA	4067
rs557759804	snp	C/G	0.0023933	0.0345097	intron-variant	LYN	GRCh38.p7	8:55991152	ACTCTGCCACCAGCC[C/G]TGACAGCTGGGTTGC	4067
rs557830046	in-del	-/G	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55985422	AAAACGCACTTCAAA[-/G]GGGTTGAAATATAAA	4067
rs557851031	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55937232	AACAAGGTGGTGGAT[C/G]TCCTCTTAGATTTTT	4067
rs557854368	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55943987	ACTTGGGAGGCTGAG[G/T]CAGGAGAATTGTTTG	4067
rs557867264	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55904884	TCAAAAGCAGGTAAG[G/T]TTGTAGTGTAGAGTG	4067
rs557878354	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55893450	GATGCTGTTCTTCAA[C/T]AAAATAAAGACTCAT	4067
rs557916828	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55880239	GCGCGGCCCGCGGCG[A/G]CTTCCTGGCCGCACC	4067
rs557942098	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55957260	GACTCCGTGTGCCCT[A/G]TTTTTATTATTGTCA	4067
rs557993682	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55925622	CCATGCGGGGATGGG[C/T]GTTATTATTACCTTT	4067
rs558004733	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55967543	CTGGTCTCGAACTCC[C/T]GAGCTCAGGCAATCT	4067
rs558007700	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55972301	GCTCAAGCTGCAAAC[C/T]TCACTCAGACTCTTT	4067
rs558028847	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55982618	GGTCCTCGGATCCCC[A/G]AACACTCCTCCTTGC	4067
rs558055250	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55918909	GGTGGACTTCAGCAG[C/T]GAGAATGGGCTGGGT	4067
rs558056404	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55957757	AGACTAGTCTGGACA[A/G]CATGGTGAAACCCTG	4067
rs558093914	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55924737	TCACCTTTAAACTCC[A/T]AGAGTGAGTTTACAG	4067
rs558103193	in-del	-/T			intron-variant	LYN	GRCh38.p7	8:55920318	TTAGCAGGATTCCCA[-/T]TCATAAAGCCTCTTT	4067
rs558115589	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55933935	GTGGCAAATAATAAA[C/G]AAGGAGCTTTGGCCA	4067
rs558137599	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55891794	CCTTGAGGATATTTC[A/G]TTAAGTTTGATAAAT	4067
rs558178823	snp	A/G	0.00478085	0.0486577	intron-variant	LYN	GRCh38.p7	8:55934260	AAATCAGGTAAACAC[A/G]GCAAACAGAAGATAA	4067
rs558205385	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55982967	TGCTTCTCTTCTCTC[C/T]TCCCCTAGCTTGGAG	4067
rs558210896	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55976994	GTTTGAGACCAGCCT[C/G]GCCAACATGGTGAAA	4067
rs558226961	snp	A/G	0.00318978	0.0398085	intron-variant	LYN	GRCh38.p7	8:55966159	TAGCCCTCATGGTAG[A/G]GTGCCAATAAAAACG	4067
rs558316161	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:56001439	CAGCCACACAGTCTG[C/T]GTGCTCCCATCACTA	4067
rs558316842	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55879088	ACATGAGCTTGAGCA[C/T]GCGGTCACACATTCT	4067
rs558317617	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55943905	CTGGCCAACATGGTG[A/G]AACCCCATCTCTACT	4067
rs558331179	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55885923	TCTACCCTCTGCTGC[A/C]CTCTGCATTTTCGGT	4067
rs558358197	snp	G/T	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:55917245	GGCTGGAGTGCAGTG[G/T]TGTGATTGTAGGTCA	4067
rs558393790	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55921114	TCTGAAACGAAAACA[A/G]TTTTGGGAGTTAACA	4067
rs558394560	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56003029	AAAGTACTTTCTTTA[C/T]GCAGTAAACTGCTGG	4067
rs558422236	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55961001	AGTGAGGCTAAGGAC[A/G]ATGTTTCCTCTGACT	4067
rs558454895	snp	A/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55954851	AAATAAATAAATAAA[A/T]AAATAAATAAATAAA	4067
rs558466694	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55997661	CTTTGGGGTAGGGGG[C/T]GGGGAATGGGACACA	4067
rs558484885	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55970826	CTCGATAGCTATACC[A/G]CTTCCATTTCAGAAG	4067
rs558488015	snp	A/G	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:56003343	TTGGATTACAGGCAC[A/G]AGCCACCTCACTCGA	4067
rs558492171	snp	C/T	0.46865	0.121211	intron-variant	LYN	GRCh38.p7	8:55911142	ACACATACATATATA[C/T]ACGTGTATATATATG	4067
rs558492826	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55973721	TTACTCTTTGGTGGC[A/G]GTATCTCTGAAGTGC	4067
rs558502881	snp	C/G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55940135	GTACAATTCCTCCCC[C/G/T]ACGAGATATTGCCTA	4067
rs558533441	snp	G/T			upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55878575	TCTGTAGGATTCATT[G/T]TTTTTTGTTTCATTT	4067
rs558541016	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55889361	GACTACAGGTGTGTG[C/T]CACTATGCCTGGCTT	4067
rs558542496	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56004639	TGCCTGCGGGTGCTC[C/T]TCAAAGTAATCTACT	4067
rs558543888	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55888983	GATGCCCAATGTATG[C/T]AACAAAAATTTTCCC	4067
rs558550240	snp	A/C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55980464	GTGCAGCCCAGAGCT[A/C/T]CTGGGCTCAAGCCAT	4067
rs558617538	snp	A/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55994511	GGTGTGACAAATGCC[A/T]TACTAACAAGTCCCT	4067
rs558663074	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55974377	CTCAAGGTATATTTT[A/G]CCCCCAGTATTAAAT	4067
rs558711869	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56006385	CTCCCAGGGTATCTA[C/G]CTCTTCCTGATACAC	4067
rs558717135	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55919781	GGGAGGGAGAATGCA[C/T]CCGTCTGGGTGAGCA	4067
rs558730369	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55883427	CTGTCTTCTAGAAAT[C/G]AATTTCTGTGCTTTT	4067
rs558734847	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55961893	TCCCACCCACACCCT[A/T]CCTGTCCCCCAGAGA	4067
rs558800556	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:56007029	TTTACCAGCATCATC[A/G]AGAGTCCTTCAGAGC	4067
rs558800593	snp	C/T	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55999927	AGTGAGCTGAGATCG[C/T]GCCATTCCACTCCAG	4067
rs558808205	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	LYN	GRCh38.p7	8:55876502	CTGGCAAGGTTTTCA[A/G]TCTCTGATAATTGGG	4067
rs558811798	snp	C/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55914594	CCAATCTCTGGAACC[C/T]TTCCTGAGGCCTCCA	4067
rs558937654	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55924992	GATTATAGACACCCA[C/G]CACCACACCTGGCTA	4067
rs558965598	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55975375	ACTTTGTGGGCACCA[G/T]TGTCCTCGTCTGTGA	4067
rs558965650	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55901152	TGATGTTCATAATGC[C/T]TTTTTTTCCCTCTCC	4067
rs558981604	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55972668	TTTCCTTCTCTATCA[C/T]GTGCCACTAATTAAA	4067
rs559003643	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55948598	TCCAGTTGCTTTAAT[C/T]CTAGCTTGCTTTTCT	4067
rs559004177	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55965999	GTGTGGTGGTGGGCA[C/T]CTGTAAACCCAGCTA	4067
rs559028799	snp	A/C	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55895430	CTAATGAAAAATATT[A/C]CAGGTTGTGAACTTT	4067
rs559047707	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55992474	CACCTGCCCTTTCCC[A/T]CACCCCAGCTCCATA	4067
rs559054827	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55972456	CTTGGCAACAAGGAG[G/T]AGGGCCTGTACGCTT	4067
rs559062424	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55932872	TGCAGGAACAGAAAA[C/G]CAAATTGCAGGCTCT	4067
rs559078011	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55900172	CAACTTGGTGCAATT[C/T]TTACTATAACCATAG	4067
rs559097600	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55881254	AGATTTAGCCATCTG[A/G]CCTTATTAGTAAATC	4067
rs559118518	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55959976	AGGCAAATCTAGAGT[G/T]AGAAAGTAGATGACT	4067
rs559123237	snp	C/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55925821	ACAACTATATTTTTA[C/T]AAAAGTAAATCATTA	4067
rs559167699	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55881064	GTTTGAGTTTCTTCA[G/T]CTTTGAGAGAGCATA	4067
rs559181188	snp	A/C	0.0023933	0.0345097	intron-variant	LYN	GRCh38.p7	8:55898442	CACAGGCACGTGCAA[A/C]CATGCCTGGCTAATT	4067
rs559184143	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55953179	AGTGGTGACATGACC[A/G]AGTCCCCACTATGGT	4067
rs559204990	snp	A/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55986793	AGCAGTGATGTGATC[A/T]TACCTCACTGCAGCC	4067
rs559220574	snp	A/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55992595	TCCCCAACCATTATG[A/T]TGGTAACAGTCTACC	4067
rs559257349	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55993096	GGCCCTCCAAAGTTC[A/T]TACCTACCTAATACA	4067
rs559284145	in-del	-/T	0.00438332	0.0466095	intron-variant	LYN	GRCh38.p7	8:55928901	CTAGGAGTTTTATAG[-/T]TTTTTGTTTTTCCTT	4067
rs559294539	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55998584	AAGCAATTACAATAG[C/T]CACCATTAAGAAAAA	4067
rs559300487	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55952977	AGTGGTTGTTGCCCC[A/G]GCTCCTTTCTATGAC	4067
rs559319271	snp	C/T			intron-variant	LYN	GRCh38.p7	8:56005279	ATAACCCTCAAGGTC[C/T]ATGCATGGTGTGGCC	4067
rs559355002	in-del	-/A	0.00517822	0.0506191	intron-variant	LYN	GRCh38.p7	8:55921122	GAAAACAATTTTGGG[-/A]GTTAACATTTATTAA	4067
rs559413253	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55946673	ACATTCACATTGTTG[G/T]ACAACCAATACCGCC	4067
rs559439955	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime	LYN	GRCh38.p7	8:56011589	GTTTATGGGGGCCAG[A/C]TAGAATTTGTTTTCA	4067
rs559447185	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55944489	CTTATTTATTCATTT[A/G]TTTATTTTGAGGTGG	4067
rs559448685	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55882115	GGTAACTAAATGAGA[A/G]TCTCCACTCAGCACC	4067
rs559503478	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55919954	TGACCCCACTCTTTG[C/T]TTCTTTGTCTGTCCT	4067
rs559533117	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55937372	AAATATGTATATATA[A/G]TTTTTTCAATCAGCA	4067
rs559533309	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55945702	ATTGAGGTGGTCTTC[G/T]GTGCCACCAAATCCT	4067
rs559593324	snp	C/G	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:55904655	CTCGGGAGGCTGAGG[C/G]AGGAGAATTGCTTGA	4067
rs559605128	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55906492	CTCCCAAGTAGCTGG[A/G]ATTACATGTGCCCAC	4067
rs559673510	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56003152	GCTAGCCCCACCTCC[C/T]GGGTTCACGCCGTTC	4067
rs559706609	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55997264	TTAACCTGACAGAAA[C/T]GACATCCTGTTCTTG	4067
rs559712177	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55888723	ATACAGTAATGGGCA[C/T]AATCCTTGGTTTTTT	4067
rs559743728	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55914737	AACAGTTTCACTACA[A/G]TATCCAGTAGATTTA	4067
rs559778839	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55964309	GCTCAAGCGATCCTC[C/T]TGCCTCTCAAAGTGC	4067
rs559807522	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55885974	GGGCGGGGTGGGAGA[C/G]AGGAGCAGTCTAGAG	4067
rs559843947	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55883613	AAAAGGACTTTCCCC[A/G]ACCTGTGCTGGGAGT	4067
rs559883338	snp	C/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55990769	AGTCATGTCCAATTC[C/G]CCCTTCTCATCATGG	4067
rs559907375	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55948131	GGCATGTGCCACCAG[A/G]CCTGGCTAATTTTTA	4067
rs559920059	snp	A/G	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55991445	TTTTCTTCTCATTGT[A/G]TGTTACAAAGGCCAC	4067
rs559959295	snp	A/G	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55932139	GTTCCTGTGCATAGG[A/G]ATACCAGAAAGAAGC	4067
rs559987027	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55977718	GGGAGTTTGAGCCCA[A/G]CCTGGGCAACACAGT	4067
rs559999478	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55972006	CTCGGTGACAGGAGG[A/G]CCTGGGGGCAATCAA	4067
rs560016271	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55984257	TGGGGGGACATTAGT[A/T]AATCCAGCACAGCTG	4067
rs560025142	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55921339	TGTCTGCAAAGAAGC[A/G]GGATAGACAGGGTCT	4067
rs560065998	snp	G/T	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:55893609	AATCCATGAAGTCAT[G/T]CTTCACTTATGCATC	4067
rs560080323	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55984783	TGGCTTCACTCGGAA[C/T]GCAGGGGGAAGCCCC	4067
rs560090401	snp	A/G	0.118235	0.212457	intron-variant	LYN	GRCh38.p7	8:55942445	TATGTGTGTGTGTGT[A/G]TATATATATATATAC	4067
rs560103918	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56001021	TAGTGTGGAGCCTGC[A/G]TGGAGTGGCTTAGGG	4067
rs560141325	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55962036	GTACTTTGTATGAAC[A/G]AATTATACCAAATGT	4067
rs560161011	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55928822	ATCATGGATCATTTT[G/T]ATGTTGTATGTAAAA	4067
rs560167141	snp	A/C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55897035	ATGAGCCACTGCACC[A/C/T]GGCCTAAACTTCATT	4067
rs560177818	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55975185	CATTGCTTGGAGCTG[A/G]TGCTTGGAAACCTCA	4067
rs560193403	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55895567	GGCCAAGGCAGGAGG[A/C]TCACTTGAGGCCAGG	4067
rs560220677	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55948828	TACTTATAAAATGGG[A/T]ATGACAGTACCTAGA	4067
rs560254318	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55889060	TCTCACTCTGTCGCC[C/G]AGGCTGAAGTGCAGT	4067
rs560342636	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55897787	GAGTGGTGGCATGGG[A/C]CTGTATTCCCAGCTA	4067
rs560366504	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55977016	ATGGTGAAACCCGGT[A/C]TCTACTAAAAATACA	4067
rs560372901	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55979882	CGCCCACCCTGGTGC[A/G]GAAGACCCCACCCGA	4067
rs560384470	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55896323	AACAAAGAAACAAAA[C/G]CAAGTTTATAAATAA	4067
rs560384856	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55973875	TGCTTGAGGCCAGAA[A/G]TTCAGGACCAGCCTG	4067
rs560398543	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:56006738	AAAGGAGGAAGGATG[A/G]AAAGTGAAACTGTGT	4067
rs560415124	snp	C/T	0.00318978	0.0398085	intron-variant	LYN	GRCh38.p7	8:55981607	GCAGTCCTCCCACCT[C/T]TGCCTCCCAAAGTGC	4067
rs560452430	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55883006	TTTAATACACTTAAC[C/T]TACTAAACATTATAG	4067
rs560463004	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55982150	GCTCTTGTTCATTTT[C/T]CACCCAGCGCCCCCA	4067
rs560467774	in-del	-/C	0.00557542	0.0525036	intron-variant	LYN	GRCh38.p7	8:55961034	TGGTCTATGAAGAGA[-/C]CCCTGAGGAAGGAAG	4067
rs560473845	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55884318	TCATGTTGGCCAGGC[C/T]GGTCTTGAACTCCTG	4067
rs560481892	in-del	-/AC	0.00318978	0.0398085	intron-variant	LYN	GRCh38.p7	8:55942276	CCACTATATATATAT[-/AC]ACACACACATATATA	4067
rs560505615	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55901272	CTCGTCCTTTAAAAC[A/G]GGAAAATTGATAGAA	4067
rs560506736	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55927344	TGGAATCACACAGTA[C/T]GTAGCCTTTTCAGAT	4067
rs560528055	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55947270	AGAAAAACCAAAATG[C/T]TACATGATGTTTATC	4067
rs560545161	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55934036	TTCGAGACCAGCCTG[A/G]CCAATATGGTGAAAC	4067
rs560592821	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55950187	ATAGGCATTTTGGTT[C/G]TTTCTACTTTTTGCT	4067
rs560620805	snp	A/G			intron-variant	LYN	GRCh38.p7	8:56007233	ATCATACTGGATGTT[A/G]GTCCTCCCACCACGA	4067
rs560631865	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55967566	GGCAATCTGCCTGCC[A/T]CAGCCTCTGAAAGTG	4067
rs560639137	snp	A/C	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:55980787	TGGTGGTAAAATAAA[A/C]ACAAATTACACCATT	4067
rs560685336	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55947472	CTGTGGGCCGTGCAG[A/G]CCCTGAGCCCACTAG	4067
rs560686910	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55926480	ATAAATGGCTATGGG[C/T]GTATTAGGAGTGATG	4067
rs560743170	snp	G/T	0.00517822	0.0506191	intron-variant	LYN	GRCh38.p7	8:55934597	GACAGGCAGAATGAG[G/T]GGAGCCCTGGGACAG	4067
rs560777294	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55928004	AGACTGTCTTCCAGA[A/G]TGGTTGGGTCATTTT	4067
rs560788010	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55931875	TTTAAAAAACTTTAT[A/G]CATTTTTAATGTGCT	4067
rs560804679	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55961438	AAAAATCATGCCTTT[A/G]ACAGAGGGATGAAAA	4067
rs560820892	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55941368	GAGATTAGGTTGATC[C/T]AGCTCTCTGAAGGGG	4067
rs560833281	in-del	-/A	0.250732	0.249999	downstream-variant-500B	LYN	GRCh38.p7	8:56012717	GTGAGACCCTGTCTC[-/A]AAAAAAAAAACCAAA	4067
rs560874866	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55999646	TTACTTCATCTACCC[A/G]ATAGCAAAGAATAAG	4067
rs560941249	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55901749	ACTTCAGATATTTCC[A/G]ACGCGGAGCTGGATG	4067
rs560947150	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56006592	CTGCTCCCCACCACC[A/T]CCTTCTGGTGAGGGC	4067
rs560956330	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55987187	GGAGGCTAAGGCAGG[C/T]GGATCACCTGAGATC	4067
rs560960714	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56000062	TGCCTCCTTATTTTG[A/G]GTGTGTGTTCTTGTT	4067
rs560982366	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55899759	GGTTCAAGTGATTCT[C/G]CTGTCTCAGCTTCCC	4067
rs561016280	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55997224	TGCAGAGAGAACTTG[A/G]AGAGCCAGTTCCATG	4067
rs561017365	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55980977	CCCCCGTGCTGTTCT[C/T]GGTCTCTGTGAATCT	4067
rs561021992	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:56001213	AGGCCAGCGTGGTTT[A/G]GGCCTCTGTGAGTAT	4067
rs561028628	snp	A/C	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55901836	TTTCCTGGCTCAACC[A/C]AAGATAAGCAGGGAA	4067
rs561028987	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55914105	GTTGTTGTTGGTGTG[C/T]GTGTGTGTGTGCACG	4067
rs561041067	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55907473	GGAAGCTCTGTGTCT[C/G]GTTTTGGAAGGTGGT	4067
rs561046147	snp	A/G	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:55894434	AAGTGCAGTGGCTCA[A/G]TCTTGGCTCACTGCA	4067
rs561059895	snp	A/C			intron-variant	LYN	GRCh38.p7	8:56003759	GGAAAAAGAAAAAAG[A/C]AAGTCACATATAAGG	4067
rs561066622	snp	A/T	0.00517822	0.0506191	intron-variant	LYN	GRCh38.p7	8:55890126	TATAGACAAAAAAAA[A/T]AAAAAAAAAAAAGAA	4067
rs561074013	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55954115	ATTTATTTTGTTTTC[A/C]TCTGTCCATTGGGGC	4067
rs561144153	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55896150	TGGCATGCCCCTGTC[A/G]TCCTAGCTGCTCTGG	4067
rs561170162	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55888173	GCTACTGGGAGTCCC[A/G]CACAGTGTTAGGAGT	4067
rs561177310	snp	G/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55896540	GAGATGGCATTAGGA[G/T]AAATACCTAATGTAG	4067
rs561179320	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55994375	GGAATCTGAGCTCCT[C/T]AAAGCACTCTGGCAT	4067
rs561202455	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55920135	ATAGTAAAATAATTC[A/G]GCAGATTAATTGTGG	4067
rs561202485	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55927239	ATCCCCCATTCTTCA[C/T]ATGTTTATTCCTCTA	4067
rs561220505	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55985592	TTCAGAATAACACAC[A/G]TCAAGTTCTTTAAGG	4067
rs561260898	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55952769	GAATAGGAATGCAGA[C/T]TTGCAGATCTGTGTT	4067
rs561262351	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55920826	CTCCTGCCTCAGCCT[C/T]AGCGGGATTATAGGC	4067
rs561262946	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55945912	GGACGGCAACTCCAC[A/G]AAATCACCAGGGTCC	4067
rs561303788	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55933548	GTACTGTCAAGTTAA[A/G]GATTGTATCACTTAT	4067
rs561313070	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55897161	TATCTTCTGATTGAT[C/T]GCATTACAGTCTTGA	4067
rs561411712	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55882354	AAAGCCTTTTACTTC[C/T]ATCTGCAATATTTGT	4067
rs561422628	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55897855	GAGGTGGAGGCTGCA[A/G]TGAGTCGAGATCGCG	4067
rs561439019	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55973196	CCCCTGTCACCCATT[A/G]AGACAGAAAGTGGCT	4067
rs561467490	snp	C/G	0.00318978	0.0398085	intron-variant	LYN	GRCh38.p7	8:55987362	ACAGTGAGCCAAGAT[C/G]AGGCACTACACTCCA	4067
rs561484456	snp	A/G	0.00398564	0.0444627	intron-variant	LYN	GRCh38.p7	8:55891952	ATTGAAATGGCTGTG[A/G]TGTGGGAGAGGGAAT	4067
rs561491344	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55903283	CAGGCGTGAGCCACC[A/G]TGCTGGGCCTTGTAC	4067
rs561496441	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55892688	CCTGGGATTACGAGC[A/G]TGAGCCATTGTGCCT	4067
rs561504928	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55979764	GGTGTGTCTGGGCTC[C/G]TTGGTATGGTTTCTA	4067
rs561529066	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55935620	CTGTACTAAAAATAC[A/G]AAAATTAGCCATGCT	4067
rs561572037	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55933998	TTTGGGAGGCCAAGG[C/T]GGGCGGATCACAAGG	4067
rs561573686	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	LYN	GRCh38.p7	8:56012503	CTAAGGCAGGAGGAT[C/T]GCTTGAGCTCAGGAG	4067
rs561601032	snp	C/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55916994	CCACCCTGGCCAACA[C/G]GGTGAAACCCCGTCT	4067
rs561612124	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55967510	TAGTAGAGATGGGGT[A/T]TCGCCATGTTGGCCA	4067
rs561634963	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55983362	GTTTCAAGACACTGT[G/T]CTAGAAATTCCGCAT	4067
rs561661931	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55917381	TAGAGATAGGGTCTT[A/G]CTATGTTGCCCAGGC	4067
rs561666557	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55942583	CTAGGTCAGGAGCTC[A/G]AGACCAGCCTGGCCA	4067
rs561676906	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55943330	TTCAGGCTGGGCATG[G/T]TGGTTCATGCCTGTA	4067
rs561689217	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55895051	ACTCCTGGTCTCAAG[C/T]GATCTTCCCACCTGC	4067
rs561739763	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55936142	CATACTTTTAGGGAC[A/G]AATTCCTATAAATGA	4067
rs561743359	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55897111	CGATGTTACTCACCC[A/G]AACGCTGGCTTTATG	4067
rs561814304	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55982745	GTCTTGACTTCCTCC[A/C]CTCCAAGACTCTGTC	4067
rs561826312	snp	A/G	0.000215127	0.010369	intron-variant	LYN	GRCh38.p7	8:55954018	GATCTATGTCCTTCT[A/G]GAGATGGTGACAGGA	4067
rs561828665	snp	C/G	0.0023933	0.0345097	intron-variant	LYN	GRCh38.p7	8:55930110	TGAAACCACCACCCC[C/G]CACCTGACCCCGCTC	4067
rs561849722	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55936507	TAGCCAGGTGTGGTG[G/T]TGGGCACCTGTAATC	4067
rs561858676	in-del	-/A	0.00597247	0.0543191	intron-variant	LYN	GRCh38.p7	8:55988880	CTTCTCATTAAAGTG[-/A]AAAAAAAAAAACCCA	4067
rs561862588	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55932011	CCAACACATATGACA[G/T]GCTTAAACTTTAGTT	4067
rs561882406	snp	G/T	0.00199481	0.0315187	upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55879217	GCATGCGGGCAGTGC[G/T]GGCCCTGTACAGAAA	4067
rs561895043	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55885668	AAATGTTAACCCCCA[C/T]GGAGGTGAGGGGAAT	4067
rs561897303	snp	A/C/G	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:55930111	GAAACCACCACCCCC[A/C/G]ACCTGACCCCGCTCT	4067
rs561907601	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55962867	CCTCAGGAAGCTTCC[A/G]TTCAAAAAGGAAGGC	4067
rs561909509	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55883727	GGCTCATAGGACGCA[C/T]ATTAAAACACCTGAT	4067
rs561911649	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55928280	CCTCTGGAGTAGCTG[G/T]GACTATAGGCAAGCG	4067
rs561942430	snp	C/T	0.0023933	0.0345097	intron-variant	LYN	GRCh38.p7	8:55918486	AATCATTGCCTTCTG[C/T]ATCAACAGGACAAAT	4067
rs561943652	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55987576	TGCCCGCCACCACAC[C/G]TAGCTAAGTTTTGTA	4067
rs562002400	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55984283	AGCTGTCTAGACTCC[A/G]GCCACTCCGAAGCTT	4067
rs562032671	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55936569	TGCTTGGGCCCGGGA[A/G]GCAGAGTTTGCAGTG	4067
rs562075958	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55996400	CAGATGACTGGGGAA[A/G]GTCAGATCCTCCAAG	4067
rs562088612	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55890618	TGTGGGGTCTCAGAG[A/G]TGTTTGTACACTTGT	4067
rs562092707	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55935051	CCACGGGCCATGGTC[A/G]TAGCCTAGAGGTGAC	4067
rs562119817	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55922706	TGGCAGGCGGAGGCT[A/G]CAGTGAGCTGAGATT	4067
rs562153809	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55928665	TTTTGCAAAGATTTT[A/G]TTTTAATCTGTGGCT	4067
rs562156786	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55960001	ATGACTGGTTGCCTA[C/G]GGCTGGGGGGCCTGG	4067
rs562181403	snp	A/G	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55923306	AAGCAGGTGGGTCCC[A/G]GTGCCAGGAGAACTG	4067
rs562239286	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55902934	ACTCACTGCAACCTC[C/T]GCCTCTTGGGTTCCA	4067
rs562279235	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56008162	AATAAAATACTGGTA[A/G]TACTCTAAAAAAGTC	4067
rs562298197	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55915801	AGAGAGAAAGAGAAG[A/G]AAAGAGAGAGAGAAG	4067
rs562395163	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55909346	GGGACAGTGGGGACC[A/T]GCCATCCAGGGCCAA	4067
rs562405703	snp	C/T	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55903053	AGGGTTTCACCATAT[C/T]GGCCAGGCTGGTCTC	4067
rs562406323	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55949426	TTTTAATTCCATCAC[A/G]GAGAGTGAATTTTCC	4067
rs562485604	snp	G/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55949331	GCCATTTGTACCAAC[G/T]CTTCTTTGTGCACCC	4067
rs562517911	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55980938	AATGCCAGCTCCCCG[C/T]GGCCGCTTGCTAGCC	4067
rs562547586	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55935971	TTTGGAGAAAGCATT[C/T]AACTCTTCTGAAGAC	4067
rs562548009	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55926813	GTGTCTGTGCTGCCA[C/T]AATATACTTTTAAAA	4067
rs562603026	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55956812	AGGAAAACCAGGATC[G/T]CAATCACACTTAATT	4067
rs562606477	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55909877	TTAATGATTAGTGAT[A/G]TTGAGGATTTTTTTC	4067
rs562612642	snp	A/G	0.0023933	0.0345097	intron-variant	LYN	GRCh38.p7	8:55982183	GTCTGTAACATCATT[A/G]TCTGGCAATGTTATA	4067
rs562625601	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55891907	TTCGTCATTTAATAC[A/G]TGGCCACGTGGATTG	4067
rs562627651	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55970165	GTTTTATTTAAGTTA[A/C]GAATCGAATGTATGG	4067
rs562635826	in-del	-/C	0.00319297	0.0398282	utr-variant-5-prime, frameshift-variant	LYN	GRCh38.p7	8:55879946	GGGGCGGCCGCGCCA[-/C]CCCCGGCCCCGCGCC	4067
rs562646559	snp	C/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55975726	AGAATTGCAAAAGTG[C/G]ATCATATGCAGTTTC	4067
rs562665552	snp	C/G			missense	LYN	GRCh38.p7	8:55953868	GAAGATTGGAGAAGG[C/G]TTGTATTAGTCCCAA	4067
rs562690061	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55975069	GAAAAACAGCCAGCA[C/T]TGAAGAAGGCATTCA	4067
rs562711086	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:56006805	TTTCTTTAACTTAGC[A/G]ACAGGCCAACACCAA	4067
rs562736934	in-del	-/AAAAGATA	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55887103	CTTTGTAAATATCTT[-/AAAAGATA]AAACATTCAATTACA	4067
rs562756606	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55976476	CACCCTCTTGGTGTG[A/G]CCCGCTCCCTTTCAC	4067
rs562800822	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime	LYN	GRCh38.p7	8:55877720	CGCCTTCTCTTGCCC[C/T]GCCCATCGTATTCCT	4067
rs562821408	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55970571	AAGAGATTTATAGAA[C/G]TTCTAGGGAAGACTG	4067
rs562835270	snp	A/G	0.00478085	0.0486577	intron-variant	LYN	GRCh38.p7	8:56001026	TGGAGCCTGCGTGGA[A/G]TGGCTTAGGGATTGG	4067
rs562877011	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55903200	ATTTCACCATGTTGG[C/T]CAGGCTGGTCTCGAA	4067
rs562878353	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55934480	TGCCGTTCACCGGCC[C/T]GCTAAGATTTGACTG	4067
rs562941303	snp	A/G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55928177	TTGAGACAGAATCTC[A/G/T]CTCTGTTGCCCAGGC	4067
rs562984964	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55914256	GGAGTGGAGAAGAGA[C/T]TGAGGACTCAGGCAC	4067
rs563027007	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55971890	ACCTTCATAGCTTAC[A/G]AGGAAGATTACCACA	4067
rs563057514	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55928513	TTCATGTACTTATTT[A/G]CCATCTGTAGCTCTT	4067
rs563060020	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55969509	CTCACCTGGAGCACA[C/T]GCCATGTTTCACATC	4067
rs563068828	snp	G/T	0.0023933	0.0345097	intron-variant	LYN	GRCh38.p7	8:55994811	TGCACTACCATGGAG[G/T]GGAGCCGGGAGGCTG	4067
rs563071394	snp	A/C/T	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55880110	CGCGAGCGGGTGAGT[A/C/T]CTCTGCGCGAGCCCA	4067
rs563091462	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55972409	TGGCTTTTCTTATTA[C/T]AATACAGATAATTTG	4067
rs563118407	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55962082	GCCTCTTTTACTCAA[C/T]GGGTTGGTGAGAGGC	4067
rs563122148	snp	G/T			intron-variant	LYN	GRCh38.p7	8:56009358	GCTAAATTTATTTAT[G/T]GAGTTGCTTGCAGAA	4067
rs563141106	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55922475	GTAGAAGACAGTCTC[C/T]GAAGAATTATAAACG	4067
rs563170098	in-del	-/CCAAACAC	0.00874735	0.0655527	upstream-variant-2KB, frameshift-variant	LYN	GRCh38.p7	8:55879716	TGCGCGACGGCCACA[-/CCAAACAC]CCAAACACCCAAACC	4067
rs563180260	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55932036	TTAGTTTCTGAGAAG[A/G]TGAAATTAGGATGTG	4067
rs563188591	snp	A/G			upstream-variant-2KB	LYN	GRCh38.p7	8:55877165	TCCTGCCTGCAGGAC[A/G]GTTCTCCAGTGGGCA	4067
rs563202512	snp	A/G	0.00993419	0.0697739	intron-variant	LYN	GRCh38.p7	8:56002406	CCTGGGTGACAGAGC[A/G]AGACTCCATCTTAAA	4067
rs563222139	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55886977	AAACAGTATATTTGT[A/G]TCCATTAATCAACAT	4067
rs563248017	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55886273	TGAGATGGAGTCTCG[C/T]TCTGTCGCCCAGGCT	4067
rs563273857	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55998554	GTTTTATTTTGTTTT[C/T]GTCTGTTTTTGACAA	4067
rs563304113	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	LYN	GRCh38.p7	8:56011573	GAACACCTGAACATC[C/T]GTTTATGGGGGCCAG	4067
rs563325968	snp	A/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55924077	TTTCTTTTTTTTTTT[A/T]ATTATAGCAACCACA	4067
rs563342538	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56004227	GTGAGTCACCGCACC[C/T]GGCCTAAATATTTTA	4067
rs563357071	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55958832	TATTCCTTTATATGC[A/G]TACATAACCTTTTGT	4067
rs563395479	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55912152	TGCAAGAAAAGAAAT[G/T]ATGGTAAAAATAAAT	4067
rs563441469	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55965120	ATATTTCTGCTTTGC[C/T]AAATTACTGAGAAAA	4067
rs563454872	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55925641	ATTATTACCTTTTTC[A/G]TGGGTGAGGAAGCAG	4067
rs563469743	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:56003630	CAGTGAGCCGAGATG[C/T]GCCACTGCACTCCAG	4067
rs563519665	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55918973	GGAGTTCGAGGCAGG[A/G]GAATTGCATGAGCTC	4067
rs563537704	snp	C/T	1.65581e-05	0.00287728	synonymous-codon	LYN	GRCh38.p7	8:55950759	CGCTGGAGCTTTCCT[C/T]ATTAGAGAAAGTGAA	4067
rs563555868	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55964196	CCATATGTTCTAACA[C/G]TTATCTTGTACTGCA	4067
rs563609494	snp	A/T	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55944821	AAAGATGTCCTTTAT[A/T]CAGAAAAGTCAAGGA	4067
rs563640014	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55878295	TGAGGAGTTAGGGAG[G/T]TGGGGATCTGGTTGC	4067
rs563661703	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55963554	AGCTGCTCCAGAGTC[C/T]CTCCCAAGGGGCAGG	4067
rs563667080	snp	A/C	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:56009369	TTATTGAGTTGCTTG[A/C]AGAAATTTCCTTAGC	4067
rs563676524	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56002376	GTGAGCTGAGATCGC[A/G]CCACTGCAATCCAGC	4067
rs563694501	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55944166	TCTTGATAAATTAAC[A/G]TTGTAATTTTATATA	4067
rs563722183	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55956799	TGAGAGTATTGGCAG[A/G]AAAACCAGGATCGCA	4067
rs563735471	in-del	-/T			intron-variant	LYN	GRCh38.p7	8:55901642	GGTCCTGCATGAATA[-/T]TTTCAGTGCTGATTC	4067
rs563747070	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55916757	ATGCCCAATACTGCA[A/G]TGGCACCTTAGGCTG	4067
rs563763185	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55910168	AAGTCTCATTTGTCT[A/G]CTTTTGTTTTTGTTG	4067
rs563766170	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55996601	GTTTCCTTCCTTCCT[G/T]CATTTCCTTGTTCCT	4067
rs563827508	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55977139	GCAGTGAGCCAAGAT[C/T]GTGCCACTGCACTCC	4067
rs563838008	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55977611	TGGGAGAGTTTGTGT[C/T]CTAGCCCAGAGCTCA	4067
rs563854515	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55966396	TAATTGAGACGGAGT[C/T]GCACTCTGTCACCCA	4067
rs563870598	snp	A/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55886239	CAGTGGCTGTCAAAC[A/T]TCTTTTTTTTTTTTT	4067
rs563893192	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55886677	CCCTCCCCTTAACTT[G/T]CAGGGGAATGTGGCC	4067
rs563903023	snp	G/T	9.98187e-05	0.00706395	utr-variant-3-prime	LYN	GRCh38.p7	8:56010141	GTCCATTTGGCAGGG[G/T]TGGCTGCCTCATTTA	4067
rs563908912	snp	C/T	0.00636936	0.0560724	intron-variant	LYN	GRCh38.p7	8:55903979	TGGGCTGTGATTGTG[C/T]CATTACAACAGAGTA	4067
rs563924596	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55990605	TCTTCTTTAGAACCT[A/G]TTATCTGTCATGTGA	4067
rs563946658	snp	A/C	0.001998	0.0315437	utr-variant-5-prime, missense	LYN	GRCh38.p7	8:55879945	CGGGGCGGCCGCGCC[A/C]CCCCCGGCCCCGCGC	4067
rs563972026	snp	C/T	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55898374	GCTCACTGCAACCTC[C/T]GCCTTCCGTGTTCAA	4067
rs563977584	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55936693	TAGAAGGAATAGATT[C/T]TAGGTTCTACAGCAC	4067
rs564004144	snp	A/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55983407	ACTTCTGCACTTCCC[A/T]TAGGAATCAAAGTAA	4067
rs564020089	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55892777	TAAAAAGTTTTCCCA[A/G]TGCAGGAGTGTGTGT	4067
rs564034682	snp	A/G	3.34085e-05	0.00408695	intron-variant	LYN	GRCh38.p7	8:55941826	TTCTGGAATGGTAAA[A/G]CAATGTCATTACTTT	4067
rs564034889	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55934510	GGGCACTGCTGATTC[A/G]AGGGATGTTAAATGG	4067
rs564062093	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55936199	TGAAACTCAAGATCA[C/G]TTTTGTTTCAGATAG	4067
rs564074236	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55936562	GAAGAATTGCTTGGG[C/T]CCGGGAGGCAGAGTT	4067
rs564091811	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55971778	CTGAGTCTTTAATTT[A/G]GTGAATTACTACCAT	4067
rs564142006	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55930913	CAGCTTGGCCTCCAG[C/T]GCACTGGGATTAGAG	4067
rs564173438	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55924935	CAGCCTCCGCCTCCC[A/G]GGTTCAAGCGATTTT	4067
rs564187833	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55918111	AGCAGCAGCTTGCAG[A/G]TCTCCCAGCGCTGAT	4067
rs564255534	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55911666	CTGGTAACCCTGGGG[C/G]CAGTCCTATGAGCTG	4067
rs564291591	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55924599	GAACTCCTGACCTCA[C/G]GTAATCCACCCCCCT	4067
rs564355254	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55917587	ATGAACTGTGACAGG[A/G]GCTAGCAAGAAAGAA	4067
rs564413410	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56001995	ATTTTTTGAAAAAAG[A/G]ACTGGCTGGGCACGG	4067
rs564430765	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55997807	TGTTAAGACATGGCC[A/G]GGCGCGGTGGCTCAC	4067
rs564445538	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55916665	CTCCCTCCTCCCCTG[A/G]GAGTGGAGCCAGGCT	4067
rs564467131	snp	C/T	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55970116	GAGGCAGTTCCATGC[C/T]ATGTAAGCACAGCAG	4067
rs564501465	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55946860	CCTTTTGTGTTTGGA[G/T]TATTTCACTTAGCCT	4067
rs564522447	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55926551	AGTTATTTTCTGAAC[A/C]TAAAATTGAAGAAGT	4067
rs564536771	snp	A/C/G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55933232	TCTAATATGACATTA[A/C/G/T]GTAAATCTGAAATAA	4067
rs564549365	snp	C/G	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:55946059	AAGCCCTGCACAACC[C/G]ATCTGCGGACCAAAA	4067
rs564580890	in-del	-/T	0.00795532	0.062565	intron-variant	LYN	GRCh38.p7	8:55964147	AAGGACCTAGGATGG[-/T]TTTTTTTTTGTCAGC	4067
rs564592573	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55909425	GGATTCTGACTTGGA[C/T]ATGTTCAGTCATAAT	4067
rs564598542	snp	C/T	0	0	intron-variant	LYN	GRCh38.p7	8:56002373	GCAGTGAGCTGAGAT[C/T]GCGCCACTGCAATCC	4067
rs564616568	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55959655	TGCCATTGTGAGAAA[C/T]AATACAAAAAGGATA	4067
rs564628563	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55939098	TATATTGTATTTTCT[A/G]CATTTCTGGTACTTT	4067
rs564692779	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55953412	AGCATTTTGGGAGGC[C/T]GAGGCGGGTGGATCA	4067
rs564703612	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55910137	CTTTTGCTGTGCAAA[A/G]CTTTTTAGTTTAAGT	4067
rs564767479	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55992053	TAGCTTCACACATCA[A/G]CTTTCTGAGACAGAG	4067
rs564776710	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55920051	GAAAAAAGTCAATGC[C/T]AATTGAAAAAGACAT	4067
rs564783563	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55984225	CACATTCTGAGGTTC[C/T]GGGTGGTCGTGAGTT	4067
rs564790850	snp	A/C	0.0023933	0.0345097	intron-variant	LYN	GRCh38.p7	8:55912733	CTCCATCTGAAAAAA[A/C]AAAACAAAACAAAAC	4067
rs564797904	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55903342	TGAGCAGCTCTTCTT[C/T]GAGGTGTTTATTTGA	4067
rs564808497	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55897868	CAGTGAGTCGAGATC[A/G]CGCCACTGTACTCCA	4067
rs564815567	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55994055	AATCAGCCAAAGGAG[A/T]CTCTGATTTCTTCCT	4067
rs564853354	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55968695	ATGAGATAGCATAAC[A/G]TTTACTGAGCACTTG	4067
rs564864725	snp	A/G			intron-variant	LYN	GRCh38.p7	8:56008398	GGAAATTCGTTGTGA[A/G]GAATGGAGCCCCTCT	4067
rs564947573	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55993138	TCATGTTTAATTTCT[C/T]CTGTTAAGGATGCCT	4067
rs564962077	snp	C/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:56005534	ATGGGCCGCCTTGCC[C/G]GTTGTCAGTGCCCCT	4067
rs564979663	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55967007	CAAACAGTATACCCA[C/G]TACCGAAAAATCAGG	4067
rs565034453	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55905200	CGGATCACCTGAGGT[C/T]AGGAGTTCAAGGCCA	4067
rs565109562	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55906636	TACTGGGATTACAGG[C/T]GTGAGCCATCACGCC	4067
rs565139844	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55993751	TATTAATATCCATCT[A/T]CCTACCCACCTACCT	4067
rs565146519	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55932933	CATATGGATGTAAAG[A/G]TAGGAGCAATAGACA	4067
rs565149386	snp	A/G	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55997945	AAAAATTAGCCGGGC[A/G]TGGTGGTGGGTGCCT	4067
rs565184607	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55991937	GAAGCATCAGCACAT[C/T]TCAGCTTAAGTCAAG	4067
rs565196107	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55987107	GCATTGTATTTTTAG[A/C]ATAGAATAAAAAGAA	4067
rs565216292	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55947940	AGCACACTTCAGGGG[G/T]TTTCCCTTTGAAGAC	4067
rs565233554	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55958717	AATCATACAGTATTT[A/G]TCTTTTTGTCTCTGG	4067
rs565235923	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55951401	CTGGGCGTGGTGGCT[C/T]AGGCCTGTAATCCCA	4067
rs565243230	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55899622	TGTGTGAAGTTGGTA[C/T]AGTTATCATCCCTTT	4067
rs565297348	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55945074	TATGACAAAATGCAC[A/G]CTATGGATTGATTAA	4067
rs565297849	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55951885	TGCATATTTGTATCA[C/G]AAAATGTGTACTGCA	4067
rs565305011	snp	A/G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55965199	GAAGGGTGGTGCCTC[A/G/T]GGGGAACTATACTAA	4067
rs565306579	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55894245	TTGTTCTGTTGCTGA[A/G]GCTGGAGTGCAGTGG	4067
rs565327537	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55966026	GCTACTCAGGAGGCT[C/G]AGGCATAAGAATCGC	4067
rs565328993	in-del	-/T			intron-variant	LYN	GRCh38.p7	8:55886159	ATAATTTTTAAATAC[-/T]AACTATAATAATTCA	4067
rs565412070	snp	C/T	0.00398564	0.0444627	intron-variant	LYN	GRCh38.p7	8:55991895	AAAAATGTGCATTGG[C/T]CATGCTATTTGAATC	4067
rs565451852	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55978443	AATTAGTTTTGCTGT[A/T]CTGGGTTTGAAGTGC	4067
rs565453609	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55985553	TTTTCGGAGCCCAGG[C/T]GCTGTCTTTATACAG	4067
rs565494924	in-del	-/A			intron-variant	LYN	GRCh38.p7	8:55942575	GCAGATCACTAGGTC[-/A]GGAGCTCGAGACCAG	4067
rs565521827	snp	C/T	0	0	intron-variant	LYN	GRCh38.p7	8:56003208	GGGACTACAGGTGCC[C/T]GCCACCACGCCCAGC	4067
rs565549798	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55992011	TCATTTTTGGTAATA[C/G]GGATGCTTTTTATTT	4067
rs565578135	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55984478	TGTCCTTGGAGCTGT[C/G]AGATCCCAACACTCA	4067
rs565587375	snp	C/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:56003849	GGTCAAGAGATAATA[C/G]GTTATATTAATTTTC	4067
rs565622158	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55888519	AAGAGCGAAGACACG[G/T]TGAACACTGACTTAA	4067
rs565631056	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55893852	GCTAGAGTGCACTGG[C/T]CATTCACAGGCACGA	4067
rs565631869	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56003336	AAAGTGCTTGGATTA[C/T]AGGCACGAGCCACCT	4067
rs565646304	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55925059	GTTGGCCAAACTGGG[G/T]TGATCCGCTTGCTTC	4067
rs565655833	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55904854	ACATTATTAGACTGC[A/G]CATTTTACCCTTTTT	4067
rs565656996	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55917836	GGCTGGAATAGATTT[C/T]CCCAAATCTCCTGAT	4067
rs565675888	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55951591	GATCGTTTGAGCCCA[A/G]GAGGTGGAGGCTGCA	4067
rs565718412	snp	G/T	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55918454	CTTACAAGCTCTAAT[G/T]TGCAGCCAGGATTAA	4067
rs565720223	snp	C/T	0.408871	0.193029	intron-variant	LYN	GRCh38.p7	8:55911126	ATATACGTATATATA[C/T]ACACATACATATATA	4067
rs565841746	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55998022	CCAGGAGGTGGAGCT[A/T]GCAGTGAGCCAAGAT	4067
rs565850790	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55978742	GGAGTTCTGACACGC[A/G]GTCAGAGAGCAGGGA	4067
rs565862154	snp	A/C/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55972805	TCTATACCTTCCCCC[A/C/T]ACTTTACTATTTAGG	4067
rs565879924	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55945973	GGTGTTTGCTTTCTA[C/T]GTGAAGACTCCAGCC	4067
rs565895770	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55905379	GTGCCATTGCACTCC[A/T]GCCTGGGCAACAAGA	4067
rs565917942	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55977964	TCGTCTCTAAAGGGT[A/G]CACTCTGAAACGGAC	4067
rs565938845	snp	A/G			utr-variant-3-prime	LYN	GRCh38.p7	8:56011304	TCTGTATCACATGAT[A/G]TGTTTCACTTATGCT	4067
rs565957682	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55899916	AAAGTGCTAGGATTA[C/T]AGGCATGAGCCACCG	4067
rs565959117	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55970833	GCTATACCGCTTCCA[A/T]TTCAGAAGCCCTTTG	4067
rs566010402	in-del	-/AACAAC	0.00597247	0.0543191	intron-variant	LYN	GRCh38.p7	8:55897913	AGGCCCTGTCTCACA[-/AACAAC]AACAACAACAACAAC	4067
rs566039107	snp	A/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55964554	ATTTCTTTATTATTT[A/T]AAAAAATCATTTTTT	4067
rs566050751	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55996734	AAACCTGACTTTGGA[A/G]CGATACTACACTTTC	4067
rs566056251	snp	C/G	0.00478085	0.0486577	intron-variant	LYN	GRCh38.p7	8:55996520	CCAGATAAACTACTA[C/G]TTGGCTTTCTTTACT	4067
rs566074190	in-del	-/C	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55970842	CTTCCATTTCAGAAG[-/C]CCTTTGCCTATTTGG	4067
rs566089364	snp	A/G	0.00358779	0.0422022	intron-variant	LYN	GRCh38.p7	8:55989727	GAGGTTTATTTTGCC[A/G]AGGTTGAGGACCATG	4067
rs566102987	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55901420	GAAAGGAACTGTTTA[A/G]TTGAACGGTTTCATC	4067
rs566107786	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55897438	GCACATGGTGGTTTC[A/G]AGGGGTTGACAGCAG	4067
rs566117680	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55982946	TCCCTACCGCCCCTC[C/T]GCTCCTGCTTCTCTT	4067
rs566133932	in-del	-/TT	0.00358779	0.0422022	intron-variant	LYN	GRCh38.p7	8:55989667	AAAACTTTGGTCTCA[-/TT]TAACCAAACCAAAAA	4067
rs566169297	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55897918	CCTGTCTCACAAACA[A/G]CAACAACAACAACAA	4067
rs566178990	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55976953	ACTTTGGGAGGCCGA[A/G]GTGGGTGGATCACCT	4067
rs566183300	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55898415	CATCTCAGCCTCCCA[A/G]GTAGCTGAGACCACA	4067
rs566193567	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55983566	AACCTCCCACCCCTC[A/G]ACCCCAGCAGCACAA	4067
rs566199969	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55884415	TGGCCTTTCTGGGGT[A/T]TATTTGGCTTAAGTT	4067
rs566206773	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55924654	CACGCATGAGCCACC[A/G]CGCCCAGCTGCATCC	4067
rs566236488	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55919828	CTGAGGTGTGAGGCT[C/G]GGGAAATGGCTCTCC	4067
rs566257776	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55940916	TGTCCTAGCATGGCT[G/T]GCGGAGACCGTCATT	4067
rs566273547	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55924399	ATGGAGTCTTGCTCT[A/G]TGATCCAGGCTGGAG	4067
rs566279824	snp	A/C	0	0	upstream-variant-2KB, missense	LYN	GRCh38.p7	8:55879481	TGGAAGGGATCAGAG[A/C]GCACCTCCTCCGCTC	4067
rs566327658	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55934694	GAGAAGAGCCAACTC[A/C]TTATTCAGACCCAGA	4067
rs566346181	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55899936	ATGAGCCACCGTGCC[C/T]AGCCTTATCATCCCT	4067
rs566433362	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55961690	TCCATGAGCTTCATT[G/T]TTTTTATGATGGCAA	4067
rs566450125	snp	C/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55896218	GAGGCTGCAGTGAGC[C/T]ATGATTATGCCACTG	4067
rs566458400	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55974359	GCCAAGATGGAGGTT[A/G]TGCTCAAGGTATATT	4067
rs566512283	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55986718	AGCTTTAACTTGACT[A/G]TTTATTATGATTATT	4067
rs566524168	snp	A/C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55987281	AGCTGAGTGTGGTGG[A/C/T]GAGTAGGTCCCAGCT	4067
rs566538681	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55949625	TATTTTGATACATGT[A/G]TGCAGTGTGTACGGA	4067
rs566599657	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55919691	AAAACCCTAATCTTC[C/G]TCTCACCAGGCCAAG	4067
rs566603929	snp	G/T	0.000399281	0.0141238	downstream-variant-500B	LYN	GRCh38.p7	8:56012617	CCAGCTACTCAGGAG[G/T]CTGAGGTGGGAGGAT	4067
rs566605902	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55888714	GAGTGACAGATACAG[C/T]AATGGGCACAATCCT	4067
rs566608210	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55952298	GCACAGTGGCTCACG[C/G]CTGTAATCCCAGCAC	4067
rs566627032	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55883359	AATTGTCTGAACTAA[C/G]TGGCTAACTGCTCAG	4067
rs566644377	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55929781	CTGGCTTGAAATGTC[A/C]GTAGTGCTGAGGTTG	4067
rs566689194	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56005238	TCATACAGTTTTGCC[C/G]TAATGTCTGGTTTAT	4067
rs566733688	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55921901	AGCATTTACAAGTGC[C/T]GAACAATGTTTCTTG	4067
rs566765233	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55926329	TGATTGAGAGCAATG[A/G]TTCTGCAGGATTAGT	4067
rs566777612	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55972709	TTCCATAGTGCATAA[C/T]ATGACAATAGAATTA	4067
rs566779633	snp	A/G			intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55922908	GCTGTTGTAGCAATT[A/G]ATATTAGGTAGGGTT	4067
rs566847739	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55881842	TGAAAACTGCTTCAT[C/G]TGTCTTGTCCAAAAT	4067
rs566871133	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55933146	TAAAAAAGAATTACT[A/G]TACTCTTAAGCTATG	4067
rs566874304	snp	G/T			intron-variant	LYN	GRCh38.p7	8:56006435	TGTGACTGAAGACTG[G/T]CATAGTTTGTGGTAC	4067
rs566883423	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55933598	TGATTTCATTTTATG[C/G]TGAGGCAATTACAGT	4067
rs566886393	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55979377	GGTTTTCTTCTGTGA[C/T]GGAATAAAATGAAAT	4067
rs566943224	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55908397	TTACAGGCACCCCCC[A/C]CCGCGACCTGCTAAT	4067
rs566944834	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55973345	CCATAGCCCATTCAA[C/G]ATAGATCAAGAAATC	4067
rs566958787	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55966266	CTAGATACTTTTCAT[C/T]TAGCCTCCCCTAATT	4067
rs566970978	snp	A/G	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55967021	ACTACCGAAAAATCA[A/G]GAAATATGGGAAGAC	4067
rs566976830	snp	C/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55959298	TCTTCTTTGGAGAAA[C/T]GTATGTTCAAGTCCC	4067
rs566984518	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55881450	TTACTAAGCCCTTCT[C/T]TGTAAGAGTAAGCTT	4067
rs567008867	snp	A/G			utr-variant-3-prime	LYN	GRCh38.p7	8:56010271	GAACACCCTCTAAAT[A/G]GGAAAGTATTCTGTA	4067
rs567022822	in-del	-/T			intron-variant	LYN	GRCh38.p7	8:55998117	GTTAAGACATGTTCC[-/T]TTTTTTTTTTTTAAG	4067
rs567033193	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55953160	GTTCTGGGGCCTGGG[C/G]TCCAGTGGTGACATG	4067
rs567038404	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55959856	CTTCAACATGGATGC[C/T]ATGCTGTTTTATGGA	4067
rs567043423	in-del	-/A			intron-variant	LYN	GRCh38.p7	8:55891353	GCGAAACTCCGGCTC[-/A]AAAAAAAAAAAAAGG	4067
rs567073377	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55901006	CCCCTTTCCTGTTCT[G/T]GTTTCTTGGTGGCAT	4067
rs567093808	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55947030	AGTTAGGTAGATCAC[C/G]TGTGGTCAGGAGTTC	4067
rs567139616	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55999737	AGCACTTTGGGAGGC[C/T]GAGGCAGGTGGATCA	4067
rs567196073	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55986118	AGGCTGCAGTGAGCT[A/G]TGATCCTGCCACTGC	4067
rs567213106	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55953096	TCCTCCGCCCTCCCA[C/T]TCCTGTGTGCATCCG	4067
rs567228238	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55967740	TATGTAATCATAGAA[G/T]TGCTGGAGAATAGAC	4067
rs567241261	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55992221	GATGAAGAGAATCTC[C/T]TCATTTGGTTTAGAA	4067
rs567278157	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55992744	TGGGAAGTCCAAGAT[C/T]AAGGCGCCAGTAGAT	4067
rs567301344	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55945417	TAAACATTTGAAGGA[C/T]AGTATGCAGCCATGG	4067
rs567313067	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55888834	TTGGCCACCACGCCT[A/G]GCCGAATCCCTGGTT	4067
rs567317625	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55943963	TGGCACATGCCTGTA[A/C]TCCCAGCTACTTGGG	4067
rs567371547	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55895312	GTGAAGAAGTGAGTC[C/T]CTTAGTTGGAAATAA	4067
rs567381278	in-del	-/T	0.135484	0.22223	intron-variant	LYN	GRCh38.p7	8:55924362	TTCTTGGCATCCTCA[-/T]TTTTTTTTTTCTTTT	4067
rs567386363	snp	C/T	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55925189	GTGCAGTGGTGCAAT[C/T]ACCGTTCACTGCCCC	4067
rs567402603	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55972093	TGAACTCATGTTCAC[A/G]GGTCCAGGGTCTCTT	4067
rs567405661	in-del	-/AGAG	0.0733688	0.176922	intron-variant	LYN	GRCh38.p7	8:55906734	AAAAAGAAAAAAAAA[-/AGAG]AGAGAGAGAGAGGAG	4067
rs567456762	snp	A/C	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55934111	AGCGCCTGTAGTCCC[A/C]GCTACTCAGGAGGCT	4067
rs567484805	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55980130	TGCCCAGCCCTCCTC[A/G]CTCATAATCAAGTCC	4067
rs567500376	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55918701	GGTAGGGGGCAGTGT[C/T]CTCATTGTCCAAATG	4067
rs567515681	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55893816	TTTTTTTTAGAAGCA[A/T]GATCTCACTATGTTG	4067
rs567517856	snp	C/T	0.00318978	0.0398085	intron-variant	LYN	GRCh38.p7	8:55927680	TCTCTATTAAAAATA[C/T]AAAAATTAGCTGTGT	4067
rs567547863	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55991890	AACTAAAAAATGTGC[A/G]TTGGCCATGCTATTT	4067
rs567554552	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55932540	AATTCTCCTGCCTCA[C/G]CTCCTGAGTAGCTGG	4067
rs567559803	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55997956	GGGCATGGTGGTGGG[C/T]GCCTGTAGTCCCAGC	4067
rs567583809	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55977843	AGGATTGATCGAACC[C/T]GGGAAGTTGAGGCTC	4067
rs567625963	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55906608	GTAATCCACCTGTCT[C/T]AGCCTCCCAAAGTAC	4067
rs567675316	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55913610	ATGAAATGATTCAGC[A/G]AAGTGTAAACGCCCG	4067
rs567691254	snp	G/T	0.00478085	0.0486577	intron-variant	LYN	GRCh38.p7	8:55938478	TCCCATCAGGAACCT[G/T]GTCTGCTTCCTCTCT	4067
rs567712554	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	LYN	GRCh38.p7	8:56011826	AATGTCTGCACAGCT[A/G]GTCCCTTGATTCAGT	4067
rs567744032	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55978574	ATATAAATAGGGGTT[A/G]GATGAGGTCCCCTAG	4067
rs567758233	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55965410	GTCCTTTTAGTGGGG[A/G]ATCCTTTTTCACTAA	4067
rs567760499	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55887928	TATATGATTTTAAAA[C/T]GGCAGGATATAAGGA	4067
rs567769479	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55972635	GTGCCAAGAAGGCCA[C/T]CTCTGCATTATCTTA	4067
rs567831362	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55966192	TTTTTGCTACTATTT[C/T]ATAGAAACCTTTTGA	4067
rs567878718	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55905545	GCTGAGATGTGTCCA[A/G]AATTGCTAGCTACCC	4067
rs567890762	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55915669	TGAGATTGTGCCATT[A/G]CACTCCAGCCTGGGC	4067
rs567892574	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55923685	GCTGGGATTACAGGC[A/G]CCTGCTGCCATACCC	4067
rs567930113	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56005213	CTTTAGAGACATCCT[A/G]TAAGGGGAGTCATAC	4067
rs567997447	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55959698	GCAAAAACCTGTACA[C/T]GAGTGTTCATAGTAG	4067
rs568005993	snp	C/T			intron-variant	LYN	GRCh38.p7	8:56004018	CCTCACTGCAACCTC[C/T]TCCTTCTGAGTTCAA	4067
rs568034406	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56002375	AGTGAGCTGAGATCG[C/T]GCCACTGCAATCCAG	4067
rs568054418	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55975868	AGAGGAATCATGACT[A/G]GCTGTTAAAATAGCA	4067
rs568078167	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55975405	AGATGGGAGGCACAG[A/G]TTGGGTTTCCCACAG	4067
rs568079797	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55968666	GGGCTAAGTACTATT[G/T]TTCTGTGTCATAGAT	4067
rs568087091	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56007943	GGCCAACATGGTGAA[A/C]CCCCGTCTCTACTAA	4067
rs568095929	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55978841	TTGGGTGGAAGCCAA[A/G]CCCTTGGCCTCTCTC	4067
rs568182053	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	LYN	GRCh38.p7	8:55877198	CCACAGCCTCTGGTG[C/G]TTAGCAACAACAGAC	4067
rs568206525	in-del	-/AAATT	0.0263111	0.111639	intron-variant	LYN	GRCh38.p7	8:56002610	TCCATCTCAAAAATT[-/AAATT]AAATTAAATTAAATT	4067
rs568208085	snp	A/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:56008579	CTTTATCATGCAGGA[A/T]AATGTTATTATTATA	4067
rs568251013	snp	A/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:56002451	AAGAATAAAATAAAA[A/T]AAAAATAAAAAGTAG	4067
rs568286455	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55994203	AAGAATAAAGAGAAT[G/T]AATTAATTTTATATA	4067
rs568295332	snp	G/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:56002140	ATAAAAATTAGGCTG[G/T]GTGCAGTGGCTCACA	4067
rs568328165	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55960822	TGCAGTGAACAAATA[C/T]TAGGAAGTGACCTGT	4067
rs568336975	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55929373	TAGAAAATCTCTGGA[A/T]CTGTTTCAACAGCTA	4067
rs568371512	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55906172	TGCCATCTGTTAGAA[G/T]TTCTGATCAGGATTT	4067
rs568397300	in-del	-/C	0.0023933	0.0345097	intron-variant	LYN	GRCh38.p7	8:55949380	GCTTTAGTTGTAAGG[-/C]TGTTTTCCTTTGCTT	4067
rs568403759	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55896331	AACAAAAGCAAGTTT[A/G]TAAATAAAGAAACAG	4067
rs568410158	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55999837	TTAGCCAGGCATGGT[C/G]ACGCATGCCTGTAAT	4067
rs568411618	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55988175	AGTGTTGGGGAATCA[A/G]TGAATATTAACAAGT	4067
rs568418241	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55907193	ATATCTCAGATGTTC[A/G]TTATCAGAAGAGTGG	4067
rs568438938	snp	C/G	0.230017	0.2492	intron-variant	LYN	GRCh38.p7	8:55953752	GACACTATAAGGCTA[C/G]TGTTCAACTTTTCTT	4067
rs568505449	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55921780	GTCCTGTTGGCAGGA[G/T]TGTTGATAGCAGTAT	4067
rs568517534	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55914420	GAGAGTGGAAGAAGA[A/G]AAAAGGAGAAGGCAC	4067
rs568534090	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55912105	GGGGCAAGCTACCTT[A/G]GAGATAATCATTTAA	4067
rs568581231	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55928321	CGGCTAGTTTTTGTA[A/T]TTTTAGTAGAGATGG	4067
rs568645985	in-del	-/CTT	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55885044	AGGCTTCCAGTACCC[-/CTT]CTTCTGCTCTCCCCA	4067
rs568690239	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55922148	TCTGGAGTGCAGTGG[C/T]ATAAACACAGCTCGC	4067
rs568692201	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55928879	AGCTTTTCTCCTATG[C/T]TATCTCCTAGGAGTT	4067
rs568749995	snp	C/T	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55955099	GATGGCTTTTAAACA[C/T]TCTCCAGCCCCGGCA	4067
rs568750037	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55979772	TGGGCTCCTTGGTAT[A/G]GTTTCTAAGGCAGCT	4067
rs568752775	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55981776	ACAAAACTTACTTCA[C/T]TGGTTGAAATAAAAG	4067
rs568786858	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55956455	ATTTGATTTTATCTA[C/T]AGTAATCCACCATCA	4067
rs568830334	snp	C/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55941008	ACTGGATTTGATCAT[C/G]TGAATGTTTTCATAA	4067
rs568840554	snp	A/C	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55934770	CTAGTCTTAAACCCA[A/C]TTCCCACCTCACCCC	4067
rs568859510	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55887173	TGAACACGGCCAGGC[A/G]GCCAGGCGCAGTGGC	4067
rs568869325	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55896261	GGTAGCAGAGCAAGA[C/T]TCTCATCTCTGAAAA	4067
rs568869594	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55890806	CATTACAGCTCACTA[C/T]AGACTTGACTTCCTG	4067
rs568896888	snp	A/G			utr-variant-3-prime	LYN	GRCh38.p7	8:56011014	AGGGCCTTCTAAAAC[A/G]TAAGAGTTTCCTTTG	4067
rs568897415	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55889057	GGGTCTCACTCTGTC[A/G]CCCAGGCTGAAGTGC	4067
rs568914007	snp	C/G	0.0383715	0.133092	intron-variant	LYN	GRCh38.p7	8:56002183	GCACTTTGGGAGGCC[C/G]ACTTTGTGGGCGGAT	4067
rs568969258	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55981646	TAGGTGTGAGCCACC[A/G]TGCCCGGCCAGAACA	4067
rs568987912	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55883885	TTCCAGTCAGAAATA[C/T]TGAAAGATTTCTTAC	4067
rs568988333	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56005955	CAGAGTATGGTGGTA[C/T]GCACCTGTAGTCTCA	4067
rs569002488	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55883109	AAAGCCCATTTGATA[A/G]TAAAGTGTTGAATAG	4067
rs569026511	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55884377	CACAAAATGCTGGGA[G/T]TACAGGTGTGAGCCA	4067
rs569036156	snp	A/G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56008346	GTGACCAGTGATGGT[A/G/T]TAATCTACAGCTTTG	4067
rs569086928	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55915491	AGGCGGATCACCTGA[G/T]GTCAGGAGTTTGAGA	4067
rs569110090	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	LYN	GRCh38.p7	8:56012674	CAGTGAGCTATGATC[A/G]TGCCACTGCACTCCA	4067
rs569128729	snp	A/G			upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55878547	GGCAATAGGCCCTCA[A/G]GTAGTGAATTATTCT	4067
rs569157209	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55907048	TAGAAAATCTACATA[C/T]ATCTACCTCATGACC	4067
rs569162193	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	LYN	GRCh38.p7	8:55877162	AGCTCCTGCCTGCAG[G/T]ACGGTTCTCCAGTGG	4067
rs569233846	in-del	-/TGAA			intron-variant	LYN	GRCh38.p7	8:56001244	TGATGGATGGATGGG[-/TGAA]TGAATGAATGAATGA	4067
rs569234488	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55902022	TGTACTTTCTTTTTT[C/T]TTTGAGACGAGTTTC	4067
rs569268989	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55926918	ACTCCTAGGCAGTGC[A/G]CCCAGAGCTGCAGTT	4067
rs569320856	snp	A/G	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55967596	GCTAGGATTACAGGC[A/G]TGAGCACCCAGCCTC	4067
rs569355659	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56002804	TATCTTCAGGAGATC[A/G]GGATCAGTAAATTTT	4067
rs569356264	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55993467	TCTCTTGGTACTGAG[C/G]TCTCTTGTGGGTCTG	4067
rs569388711	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55982037	GGCCTCTCCCTGGGC[A/G]CTGAACAGAGCCCTT	4067
rs569402967	snp	C/T	0.00279162	0.0372561	upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55879408	TTATTAAGAACTCAG[C/T]GAGACCCCGAGCATC	4067
rs569407884	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55986797	GTGATGTGATCATAC[C/T]TCACTGCAGCCTGAA	4067
rs569416668	snp	A/C	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55913716	AAGCACAGACGTGGA[A/C]GAAGGGATGTGTAGT	4067
rs569427569	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55974967	CCATATATAATCTCC[C/T]CTCCACGTGGAAATT	4067
rs569431236	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55953729	AGTTCACAGACTGCG[G/T]CAGGTTGGACACTAT	4067
rs569466400	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55953041	TGAGTCCCAAAACAC[A/G]GAGAGAGCAACGTGC	4067
rs569473175	snp	C/T	0.00398564	0.0444627	intron-variant	LYN	GRCh38.p7	8:55977218	AAAAATAAACTAGAC[C/T]GGTTCATTCTCAGTT	4067
rs569482837	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55997503	TGTCCTCACGTGGTG[A/G]AAGGGGCAAGGCAGC	4067
rs569537212	snp	A/G	0.00279162	0.0372561	intron-variant	LYN	GRCh38.p7	8:55997970	GTGCCTGTAGTCCCA[A/G]CTACTCGGGAGGCTG	4067
rs569541226	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55904301	CAATTATTTGGCTGT[C/T]GGGTTGATGGAATGA	4067
rs569554160	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55987330	CAAGAATTGCTCGAG[C/T]CCCGGAGGTGGAGGT	4067
rs569557685	snp	A/G	0.00398564	0.0444627	utr-variant-3-prime	LYN	GRCh38.p7	8:56010786	CAGCAGGAGGAGCCC[A/G]TGAGCACGCACAGCT	4067
rs569595474	snp	A/C	0.00159617	0.0282053	utr-variant-3-prime	LYN	GRCh38.p7	8:56010237	TGGATCCTGAAATAG[A/C]GGCTAAATTACTCAG	4067
rs569604401	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55963748	CTTTGCCTATTTCTT[C/T]TGATTTTTCTTATTG	4067
rs569604988	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55898663	ATTCAGTGATTTTTA[A/G]TATGTTCACAGAGTT	4067
rs569605038	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55904841	GGCAAGGTTCCCTAC[A/G]TTATTAGACTGCGCA	4067
rs569609017	snp	A/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55991506	CAAACAAGATAAGCC[A/T]GCCCATTAACTCAGG	4067
rs569617136	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55899277	GATAAGGAAACAGAT[G/T]CTTGGGGATAATAAA	4067
rs569621159	in-del	-/G	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:56008394	GAAAGGAAATTCGTT[-/G]TGAGGAATGGAGCCC	4067
rs569632334	snp	C/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55964365	GTCTAGCCTCATTTT[C/T]CTATAGAGCACTGCA	4067
rs569647824	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55924286	GCCTCAAAACACAGT[C/T]TGGGAATCATGGTAC	4067
rs569667483	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55911006	GGTTCAAGCGATTCT[C/T]CTGCCTCAGCCTACC	4067
rs569676157	snp	C/T	0.00517822	0.0506191	intron-variant	LYN	GRCh38.p7	8:55917172	TAGAGTGAGATTCTG[C/T]CTAAAAAAAAAAAAA	4067
rs569699391	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55957585	TGAGAGACAAGTAAA[A/G]TGAACAAAGTAATTC	4067
rs569710941	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55924610	CTCACGTAATCCACC[C/T]CCCTTGGCCTCCCAA	4067
rs569745203	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55958108	ACACACCTCAGCAGA[C/G]CTGCTTACACCCCCT	4067
rs569870164	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55984335	CCGTGAGCCCCTGCT[A/G]GCTCAGCATCTGCCC	4067
rs569888108	snp	A/C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55983785	GGTTAAACCTTGCAA[A/C/T]GTCCCAGAACTCACT	4067
rs569915667	in-del	-/TA	0.103438	0.202533	intron-variant	LYN	GRCh38.p7	8:55911148	ACATATATATACGTG[-/TA]TATATATGTACATAT	4067
rs569933966	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55894429	AACTTAAGTGCAGTG[A/G]CTCAATCTTGGCTCA	4067
rs569934232	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55893256	TTAGTAAAATTAGCT[A/G]GCATAAGCTATATAT	4067
rs569934985	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55915966	TGTTTCTATTTTAAT[A/G]CCTCTAAACTCACAA	4067
rs569969174	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55936983	CTTTTCTACCCCCCA[C/T]GTCTTTTGTCTCTGA	4067
rs569999347	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55909501	TTTATCTAGTCATCC[A/G]CTGATGGACATTTAG	4067
rs570001063	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55945175	AAGGAAAAATCTAGA[G/T]CAATAGTATATGTGT	4067
rs570018476	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55901029	GGTGGCATTTGCAGC[A/G]GTGCCTCTATGATGC	4067
rs570022559	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55970813	TCTGGCTCTGCCACT[C/G]GATAGCTATACCGCT	4067
rs570029789	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55957552	GGATAAAGCATCAAA[C/T]TGCATGCTATTTGCT	4067
rs570032449	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56002083	GTCAGGAGTTCGAGA[A/C]CAGCCTGGCCAACAT	4067
rs570066530	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55928369	CAGGCTGGTCTCCAA[C/G]TCCTGACCTCAGGTG	4067
rs570069608	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55884984	TTTTCCTTGGTATAG[A/T]ACTCTTCCATGGCAT	4067
rs570108341	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55989248	GGGAAAGATGAATGA[C/T]CTGGATGGTCATCAC	4067
rs570145823	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55943582	CTCTGTCTCAAAAAA[A/C]AAAAAAAAAAAAGGC	4067
rs570153068	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55982511	CTTGATCTTCTTTTC[A/C]ATTTCCAGACCTTCT	4067
rs570187369	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55982867	CCACTCACCCTCCTG[A/C]AGCCGCTCCAGCCCC	4067
rs570222034	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55935704	GAGAATCGCTTGAAC[C/T]CAGGAGGCAGAGGTT	4067
rs570243741	snp	A/T	0.00364962	0.0425616	intron-variant	LYN	GRCh38.p7	8:56002627	ATTAAATTAAATTAA[A/T]TTAAATTAAATTAAA	4067
rs570252809	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55892317	CCCAGCTACTTGGGA[A/G]GCTGAGGCAGGAGAA	4067
rs570267196	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55885828	AGGAAGTGATACTTC[C/G]TCCACCCCAGGCCCC	4067
rs570298174	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55897588	TTTCAAAATCTTTAG[C/T]AATGGGATATAAGCA	4067
rs570299896	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55897888	ACTGTACTCCAGCCT[C/G]CGTGACAGTGAGGCC	4067
rs570305047	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55885127	AGCTGACCGTGTATG[A/G]GAAGAGATTGTCAGT	4067
rs570313779	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56003197	CCCAAGTAGCTGGGA[C/T]TACAGGTGCCCGCCA	4067
rs570371433	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55903660	AGTTTTATTGAGACC[C/T]TCCTTTTGAAAGTAA	4067
rs570425048	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55978353	GCCTATCACAGGCAC[A/G]TAGAAATAGAGAAGG	4067
rs570433385	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55904255	ATTTTCTTTATGGCT[A/G]TAGTGTAACCAAATT	4067
rs570443226	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55970680	GGGAATACGAGATCC[A/G]AGGAATGCATGAGTA	4067
rs570458653	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55929778	TTTCTGGCTTGAAAT[A/G]TCAGTAGTGCTGAGG	4067
rs570473019	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55930151	TTGCCTTCCATGAAA[C/T]CAGTCACGGATGCTA	4067
rs570478421	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55954586	GCTCATACCTGTAAT[A/C]CCAGCACTTTGGGAG	4067
rs570480361	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55962465	ATCTTCATCTCATGT[C/T]GTGTTTGTGAGATGC	4067
rs570485999	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55878648	AGGATTCTTGATAGG[C/T]TTCAATCACACACCT	4067
rs570497096	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55916130	TGGTAAATTATCTCA[C/T]GATAGTTTCATGTTT	4067
rs570497185	snp	C/T			intron-variant	LYN	GRCh38.p7	8:56008335	GAATCCTTCCAGTGA[C/T]CAGTGATGGTATAAT	4067
rs570512062	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55956563	TGTAGTAAATAAATA[C/T]TCTGTGGGAAGTTTA	4067
rs570513393	in-del	-/TC	0.00438332	0.0466095	intron-variant	LYN	GRCh38.p7	8:55976426	TCCAGCTGACCTTTG[-/TC]TCCAGCACTTGGCTT	4067
rs570537831	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55980262	GGGTCTCACTATTTT[A/T]TCCAGGCTGGAGTGC	4067
rs570592756	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55955367	ATTCTCCGTGTGGAT[C/T]GGCATGTGTCAGAAC	4067
rs570606555	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55959314	GTATGTTCAAGTCCC[G/T]TTCTCACTTTTTAAA	4067
rs570637379	snp	G/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55988464	TCTACTTATTTTTCA[G/T]TTCCAACTTATTAAT	4067
rs570696775	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55950960	CTACTAAAAGTAATA[C/T]AGTTGAGTGTGGTGG	4067
rs570703899	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55950404	TGTGATATTTTGATA[C/T]ATGCATGGAGTATGT	4067
rs570723737	snp	G/T	0.00478085	0.0486577	intron-variant	LYN	GRCh38.p7	8:55989123	ATGCCCAGCAAGGCT[G/T]GTGATGGCTCAGAGC	4067
rs570729043	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	LYN	GRCh38.p7	8:55876981	GAACACTGAATTAGC[A/G]AATACCGAGTCACTG	4067
rs570745829	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55898068	TATGAATTTTAATAC[A/T]TGTGCAGATTCACTG	4067
rs570746801	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55981841	TGGGCCTGTGGGAAA[A/C]ACAAAGTGCAGCTTT	4067
rs570763269	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55889789	TCGAATTAATTTCAT[G/T]TGGGGGCTGAAATCC	4067
rs570809505	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55982409	TGGATTTTGGGTTTT[G/T]GGATTAGGTATGTTC	4067
rs570824646	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56007820	TGTTATAATTCATTT[A/T]AAAAAATACTGGTAA	4067
rs570828285	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56001179	CAGCCAGAGCATGGG[C/G]TTGGCCAACAGGAGC	4067
rs570845378	snp	A/G	0.00557542	0.0525036	intron-variant	LYN	GRCh38.p7	8:55914551	GGTCACAGCCCTGCC[A/G]GCCATCCACATGCCT	4067
rs570853747	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55917006	ACACGGTGAAACCCC[A/G]TCTCTACTAAAAATA	4067
rs570855600	snp	C/T			utr-variant-3-prime	LYN	GRCh38.p7	8:56011579	CTGAACATCCGTTTA[C/T]GGGGGCCAGATAGAA	4067
rs570869540	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55951669	CAACCTATTTCAAAA[A/C]AAAAAAAAAGAAAAT	4067
rs570869706	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55959057	CTACTTCGGCTGCAC[C/T]ATTTTACATTCCCAT	4067
rs570871649	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55921925	TTTCTTGCACTGATA[A/C]TACAAGGGTGTGCAA	4067
rs570903881	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55908137	GATTTGCAGGCAACC[C/T]GTTTTTTCCTCCTAA	4067
rs570911052	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55949591	GAATAATTATATGCA[G/T]TCATGGGATACAGAG	4067
rs570911800	snp	A/G	0.0023933	0.0345097	intron-variant	LYN	GRCh38.p7	8:55994911	TTTGAGCCAGGCATC[A/G]TGGTTCTATCGCCAA	4067
rs570916235	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55908856	GTATTTGACTTTATA[A/G]ATTGTTTTACTTAAG	4067
rs570931242	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55952260	TCTATAAGTGGTTCT[A/G]AATTAATCTATAGTT	4067
rs570936832	in-del	-/AA	0.499234	0.0195537	intron-variant	LYN	GRCh38.p7	8:55887563	AAAATATAAATATAT[-/AA]ATATATATATATACA	4067
rs570946194	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55902520	CTAGAAGTTGAATTG[G/T]ACAAAGTACACTTAT	4067
rs570985104	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55914189	AGGCAGGCCAGGTCA[C/G]AGGGTTTTTAGGATG	4067
rs570990602	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55903069	GGCCAGGCTGGTCTC[C/G]AACTCCTGACTTCGC	4067
rs571033335	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55920105	CTGCCAAATATGTGA[A/G]CATGGGCTGTAAATA	4067
rs571142881	snp	A/C	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55978977	CCATGCTTCCCTGAC[A/C]GCTCAGCATGCCTCA	4067
rs571144206	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55935442	TTGTTTAAATAAAGA[C/T]GGTCTGGCTAGGTCC	4067
rs571195804	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55935646	ATGCTTGGTGGCGGA[C/T]GCCTGTAGTCCCCAC	4067
rs571204625	snp	C/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55888099	GTAAATAGAACATTT[C/T]CTTAAAGAACCTTCC	4067
rs571205396	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55919441	GGAATAGAATACGCT[C/T]CACTGCCGGGTCTGG	4067
rs571245536	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55992175	TCACCCCTGGGCCTG[A/G]CATTATAATGAAGAG	4067
rs571266476	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55998101	GAAAAAAAAAGAAAA[C/T]GTTAAGACATGTTCC	4067
rs571272939	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55969459	TGGTTCTCAGACACC[A/T]GTAGTGAGAAAAGTG	4067
rs571277663	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55900072	CCAGGAATCTAATGC[A/G]CTGCCACTCGAACTT	4067
rs571287494	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55946122	TTGGAAGCACACTCA[C/T]TGAGCTGGGCAAACT	4067
rs571311970	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55904929	CAACCCTGGCTGCTC[A/C]TTAGAATCAATGGGG	4067
rs571327545	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55905405	CAAGAGTGAAACTCC[A/G]TCTCAAAAAAAAAGA	4067
rs571346960	snp	C/T	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55992678	AAAATAGCTTAAGCT[C/T]TCAAGCCTATGATCT	4067
rs571348430	snp	C/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55938490	CCTGGTCTGCTTCCT[C/G]TCTCCTGCTGTGACT	4067
rs571374826	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55946735	CATACCCATTAAACA[A/G]TAAGTCCCCATTGCC	4067
rs571386146	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55995111	CAAAATTGCCACCCC[A/G]TGTCATCTGTTTCAG	4067
rs571437545	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55939202	GTTGAGGTTTCTGGT[G/T]GGAGAGTGTCTGAAT	4067
rs571438685	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55931593	ACTTTTTTCTATTCA[C/T]TTGTACCTTTTCCCT	4067
rs571453906	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55985971	CAGGAGTTCGAGACC[C/T]GCCTGGGCAATATAG	4067
rs571462417	snp	C/G	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55988949	TCTTTGCCAATTTCT[C/G]AAAAAGCGATAGTAA	4067
rs571503771	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55932393	TTGTCAAAATCTTTT[A/G]AAACAATTATATATA	4067
rs571507402	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55944536	CCCAGGCTGGAGTGC[A/G]ATGGCACCATCTCAG	4067
rs571514973	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55895107	ACAGACGTGAACCAC[C/T]GCAGCCAGCCCCAAA	4067
rs571527270	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55888799	TGGAGTGCAGTGGTA[C/T]GATCTCACTCACCAG	4067
rs571583639	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55898470	ATTTTTGTATTTTTG[A/G]TAGAGACAAAGTCTC	4067
rs571626872	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55940533	GGCGTGTGCCACCAC[A/G]CCCAGCTAATTTTTG	4067
rs571647755	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55893160	CCTCGTCCTGTTTTA[C/T]CCTGGCGATTCAGTT	4067
rs571653156	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55958334	AACAAGTTTAGAAGA[A/G]AAGAGAATGGAGTGT	4067
rs571664528	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55970045	ACCTCTTTATGTTCA[C/T]TTCATAAGTCATAGA	4067
rs571688572	snp	A/G	0.00159617	0.0282053	intron-variant, downstream-variant-500B	LYN	GRCh38.p7	8:55968071	CCAAACAATGGCATT[A/G]TTTGTTTTAAAGCAA	4067
rs571705097	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55983685	CAGTCTCACTCCCTC[A/G]TGGCACGTTTTCCTC	4067
rs571720260	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55893733	CCAGATATACTCAGA[A/G]AGTTAAAATGTTTAA	4067
rs571756885	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55925112	ACAGGCGTGAGCCAC[C/T]GTGCCCGGCCTCTTT	4067
rs571781798	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55977795	CCTGATGGTCGTGCC[C/T]GTAATCCCAGCTACT	4067
rs571789684	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime	LYN	GRCh38.p7	8:56010874	AGAGCCTCAGAAACT[G/T]CTCTGTGTTTAGAAG	4067
rs571805554	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55924745	AAACTCCTAGAGTGA[A/G]TTTACAGTGACTCTC	4067
rs571816365	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55918660	GTTCGGGGTTGTCTC[A/G]GTTAATCCTTACTAT	4067
rs571827423	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55892710	ATTGTGCCTTGCCAA[A/G]GAAAGAATATTTCTG	4067
rs571832700	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55965327	AAATGCAGGCTTTTC[C/T]CCTGAAGGCCTCCCA	4067
rs571837586	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55883898	TACTGAAAGATTTCT[A/T]ACAGCTGTCTGGTTT	4067
rs571847188	snp	C/G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56000114	CATACTAGAATGTTC[C/G/T]GGGCATGGTTGTTGG	4067
rs571890585	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	LYN	GRCh38.p7	8:56011752	GTCCTTTCTAAAATA[C/T]TCTAAAATTATTGAT	4067
rs571909715	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55996989	AGCATGGTGAAACCC[C/T]GTCTGTACTAAAAAT	4067
rs571939385	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55893395	AGTGCCAGTCTGTGC[A/G]TAGGCATTTGAAAGT	4067
rs571951116	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:56003994	CTGGAGTGCAATGGC[A/G]CCATCTCACCTCACT	4067
rs571978277	in-del	-/T			intron-variant	LYN	GRCh38.p7	8:55955901	ATGACTATAACAGAG[-/T]TTTGTTTATCTACTT	4067
rs571991106	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55903293	CCACCGTGCTGGGCC[A/T]TGTACTTTCTTGAAT	4067
rs571991582	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55903905	CCTGTAGTCCCAGCT[A/G]GCTACTTGGGAGGCT	4067
rs572003183	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55898234	TAATGTCATATAAAT[A/T]GATTCATACTGTATG	4067
rs572021234	snp	A/T	0.000798403	0.0199641	utr-variant-3-prime	LYN	GRCh38.p7	8:56010654	TTTCCCAGATTTCAA[A/T]GATTTTTTTCCCCCT	4067
rs572069979	snp	A/C	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55935418	GGTATGTAAGGCAAA[A/C]AATCTTAGTTGTTTA	4067
rs572097404	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55927712	TGGTGGCGGGTGCCT[A/G]TAATGCCCAGCTACT	4067
rs572132164	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55935744	CGAGATCGCACCACT[A/G]CACTCCAGCCTGGGC	4067
rs572151377	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55895076	ACCTGCTTCAGCCTC[C/T]CAAAGTGCTGGGATT	4067
rs572168935	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55931814	TCTCAAATGTTACAC[C/T]GTACCAGAAGACTTG	4067
rs572185135	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55977468	GAAATTGGTCTGTTT[C/T]GACTTTTGGAGAATC	4067
rs572212418	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55936529	CCTGTAATCCCAGCT[A/G]CCTGGGAGGCTGAGG	4067
rs572220312	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55970465	GGCTTTTACTAGTTT[C/T]ATTGTGTCCATTAGT	4067
rs572269043	snp	G/T	0.000798403	0.0199641	utr-variant-5-prime, missense	LYN	GRCh38.p7	8:55879900	GGCGCCTCCGGGCCA[G/T]ACGCGCTGCAGCCTC	4067
rs572285285	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55924909	TGCGGTGGTGCGATC[A/G]TGGCTCACTGCAGCC	4067
rs572393009	snp	G/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55963998	TATTAAAAGGCTTTT[G/T]TTGGTGGAATGTACT	4067
rs572401454	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55976224	CCCAGCTACTCCGAA[G/T]GCTGAGGTAGGAGAA	4067
rs572426456	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55929388	TCTGTTTCAACAGCT[A/G]CCAGATCTGTGTATG	4067
rs572441536	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55975560	GCATTGCTCTAAATA[A/G]GGGAACACAAATATA	4067
rs572449313	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55918620	GATGTTGACCAGAGC[C/T]CTCCCAGATTGAGTG	4067
rs572461838	in-del	-/T	0.00676609	0.0577691	intron-variant	LYN	GRCh38.p7	8:55961615	TGATGACTTCCCCCC[-/T]AACCTTGGAAAGCGT	4067
rs572485395	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55884620	GCCACCATGCCTGGC[C/T]AATTTTTGTATTTTT	4067
rs572502608	snp	C/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55891127	GGAGGCCAAGGTGGG[C/T]GGATCACCTGAGGTC	4067
rs572518714	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55943662	TAGAAATATATTCCC[A/G]TTATCAAACCTTTCT	4067
rs572579957	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55966103	ACACTCCAGCCTGGG[C/T]GACAGAGCAAGACGT	4067
rs572589280	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55986436	GTGAGTTTTTGCAAG[A/G]GAAAGTAAATGGGTA	4067
rs572600394	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55983989	TGGGAAGAATCCTTC[C/T]GTACCTCTTCCAGCT	4067
rs572601511	snp	C/T	9.2165e-05	0.00678779	intron-variant	LYN	GRCh38.p7	8:55966679	GGCTAGATTTTCTGT[C/T]TTATAAAGCATGCCC	4067
rs572607714	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55882591	TTAACATTGAAAGGC[C/T]ACCACAATCATTAGT	4067
rs572609362	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55923334	CTGCTTCCCCTTCCC[A/C]GCACATCTGCTCAGT	4067
rs572623672	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56008950	AAACTACAGACAAGT[A/G]TCCTTCAGATTAACT	4067
rs572628485	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56002886	CATAATCAAGCAATC[C/T]TATTTACTTCACATG	4067
rs572656120	snp	A/T	0.00119737	0.0244387	utr-variant-3-prime, downstream-variant-500B	LYN	GRCh38.p7	8:56012017	AAAGAAAATTATTAA[A/T]TTTATCTTCGCCTTG	4067
rs572673090	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55960317	CATTGATCACCGTTC[A/G]TTTTTTAATTGTGCT	4067
rs572687436	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55986306	GCCAGCAGTGTGTGA[C/G]ATTTCCAGTTTCTCC	4067
rs572704675	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55949971	ACGAATCTACTTTTT[A/G]TCTCTGAAGACTGAC	4067
rs572744184	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	LYN	GRCh38.p7	8:55876588	GCCTGGGCATGGAGA[C/T]ATTTTAGCAGCTCAG	4067
rs572749154	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55993859	ATCAAGCTTGACCAA[C/T]TCCATGTAACTCCCA	4067
rs572750182	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55917217	GAAAGATGGGATCTT[G/T]CGCTGTCACCCAGGC	4067
rs572793400	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55960950	GGTGACATGCTTCCT[C/T]TGTGGATTGTCCTAT	4067
rs572832922	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55995424	TCCTTTTCCTACTGT[C/T]CGTCTGGTTTCTGCT	4067
rs572853012	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	LYN	GRCh38.p7	8:56011224	GCTCTAATAAGCCAC[A/G]GTGGCAGGAGGTTCA	4067
rs572907771	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55888470	GCAACTTCTTGCCTA[C/T]ACTCTTTTACAATAT	4067
rs572914111	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55918817	GATTCTGATCGGGTC[C/T]TGATGGGTGCCCATG	4067
rs572927086	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55927136	TTAGGATTCACTCTT[A/G]GTGTAGTACATTTCA	4067
rs572975622	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55911984	GCTCAATATCGTCGT[A/G]GTGTGTTCTACCACG	4067
rs572981700	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55967816	AGACTTTGAATCAAC[A/G]TCCTTCTTCCTTTGT	4067
rs572989317	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55920633	GAACAAGGATAGACC[C/T]AATTTCCCCTCATTC	4067
rs573030984	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55993113	ACCTACCTAATACAA[A/C]CTTCTTTCCTCATGT	4067
rs573032961	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55901118	AGCACTTGGGCACTT[C/T]GTGGCCGTGTGTCTC	4067
rs573041111	in-del	-/G	0.0154538	0.0865337	intron-variant	LYN	GRCh38.p7	8:55918649	TGGTGCCAGGTGTTC[-/G]GGGTTGTCTCGGTTA	4067
rs573059409	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55947274	AAACCAAAATGCTAC[A/G]TGATGTTTATCCATT	4067
rs573069201	snp	C/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55999897	AATTGCTTGAACCCG[C/G]GAGGTGGAGGTTGCA	4067
rs573082120	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55913341	AAGAATTACCTATAT[C/T]GTTTGCTACAAATGC	4067
rs573087071	snp	C/T	0	0	intron-variant	LYN	GRCh38.p7	8:55912469	GGTGGCTTATGCCTG[C/T]AATCCCGCACTTTGG	4067
rs573142268	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56003558	CTGTAATCCTAGCTA[C/T]TTGAGAGGCTGAGGC	4067
rs573235413	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55997940	ATACAAAAAATTAGC[C/T]GGGCATGGTGGTGGG	4067
rs573260234	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55951813	TTTGTCAAGTAGAAT[G/T]TTTATAGGACTTTTA	4067
rs573266671	in-del	-/GAAG	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55906462	CTCCTGGCTTCAAGT[-/GAAG]GATTCACCTTCAGCC	4067
rs573302284	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55957869	GGGAGGATCGCTTGA[G/T]CCTAGGAGGCAGAGG	4067
rs573348725	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55998275	AATTCATAAGTTTTC[C/T]GGTTTTCCTTGATGG	4067
rs573351677	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55886120	GGTAGACGTTTCGAA[A/G]TCTTTTAATGTTCAG	4067
rs573356309	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55972416	TCTTATTATAATACA[C/G]ATAATTTGAGAAAGG	4067
rs573366005	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55958648	TCTCTGGCAACCACC[A/G]TGCTACTTTCTGTCT	4067
rs573402145	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55899552	GTGCACACGGTATGT[C/T]ATTCGTTCTTCTAAA	4067
rs573404457	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55925904	CAGAAGCATACAAGT[A/G]TTTATGTAAAAATTT	4067
rs573410932	snp	C/T	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:55900549	AGCTAATTTTTTTTT[C/T]TTTTTTTTTTTGGTG	4067
rs573419338	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55973010	GCAGATTGTCACAAT[A/G]AGAGATTGGTCATTG	4067
rs573430143	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55905631	GTTAAGAGGATGGAT[A/G]GTTTCCCAGGGTTGG	4067
rs573439984	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55991879	GCAAAAAAAGAAACT[A/G]AAAAATGTGCATTGG	4067
rs573455696	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55920496	AGCATTTAACATATG[C/G]TATTTCATTTAATCC	4067
rs573483367	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55979132	CTCACTGCAACCTCC[A/G]CCTCCCAGGCTCAAG	4067
rs573519328	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55938075	GGATTAAAATCACTC[G/T]TCTAATATTCTAAGG	4067
rs573568002	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55932756	AGAATTATTATACTC[A/G]CATTTATATACCAGG	4067
rs573598405	snp	A/C	0.00279162	0.0372561	intron-variant	LYN	GRCh38.p7	8:55894757	CCAGGCTGGTCTCAA[A/C]CTCCTGATCTCAGGT	4067
rs573604865	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55938615	TTTTTCTCATTGCCT[C/T]GGCTCTGGTTTTCTG	4067
rs573615774	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55918333	CATGCAGAAGCCTAT[A/G]TGTTTGTTCCCCTGT	4067
rs573623860	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55998559	ATTTTGTTTTTGTCT[A/G]TTTTTGACAAAGCAA	4067
rs573626385	snp	A/G			upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55879018	GAAGTGGGTATCCAC[A/G]GTGCCCGAGCCTAAT	4067
rs573688022	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55924525	CCACCCACCATGCCC[A/G]GCTTATTTTTGTATT	4067
rs573688631	snp	G/T			upstream-variant-2KB	LYN	GRCh38.p7	8:55877281	TTTAATTTTTTTATT[G/T]TGGGGGGGGTCTCAC	4067
rs573698148	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55917293	TAGGCTCATGTGATC[A/G]TCCCGCCTCAGCCTC	4067
rs573706849	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55933302	GTTGAAAACCCTCAC[A/G]GAACTGGCTTTGGTG	4067
rs573741872	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55882036	TGTGGTTTCTAAAAC[A/G]GGGATTTGAGAGGCT	4067
rs573752778	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	LYN	GRCh38.p7	8:56012182	AGTCACACGTTCCCT[C/T]GATGAACAGCACACA	4067
rs573832137	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55940966	TACTCCTGGTTTCCT[A/G]ACTCAAGTAGCTTAC	4067
rs573868000	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55926475	TTATCATAAATGGCT[A/T]TGGGCGTATTAGGAG	4067
rs573881074	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55960146	GAACTATATACTTTA[A/T]ATGGGTAAATGACAT	4067
rs573914160	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55886554	GCCCAGCCTGTCAAA[C/T]TTATTTGACCACAAC	4067
rs573965611	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55966431	GGAATGCAATGGTGC[A/G]ATCTCAGCTCACTGC	4067
rs573988228	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	LYN	GRCh38.p7	8:56010528	GCTAAAATAACCGGA[C/T]ATATACATAGCATGA	4067
rs574031886	snp	A/G	0.00478085	0.0486577	intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55923761	GCCAGGCTGGTCTCG[A/G]ACTCCTGACCTCAAG	4067
rs574044752	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55879199	AATAACGCCAGCATT[A/C]CTGCATGCGGGCAGT	4067
rs574053692	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55957840	GTGTTTCCATCTACT[C/T]AGGAGGTTGAGGTGG	4067
rs574060447	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55948801	CCCTTAAACTTTATA[A/C]CTTGGTTTCTTTACT	4067
rs574093898	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55921278	GGTGCTTTGTTGCTG[A/C]CTTGGTAACCAGGTG	4067
rs574127887	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55904386	AACTTTACTGAACAC[C/T]AGCAAATGTATTTAC	4067
rs574135039	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56004086	TACAGGCATGTGCCA[A/C]CATGCCCAGCTAATT	4067
rs574164468	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55903089	CCTGACTTCGCGATC[C/T]GCCCACTTCAGCCTC	4067
rs574195840	snp	A/T	0.00358779	0.0422022	intron-variant	LYN	GRCh38.p7	8:55904621	CAGGTGCGGTGGCTC[A/T]TGCCTGTAATCCCAG	4067
rs574246398	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55997735	CATAATAACATCTAT[A/G]TATCTACATGGATGA	4067
rs574304234	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56006633	CTGGGCTGTGTGCCA[A/T]TTGAGGATGATGCTC	4067
rs574326945	snp	A/G			intron-variant	LYN	GRCh38.p7	8:56004555	CACCTCAGCCTCCCA[A/G]AGTGCAGGGATTACA	4067
rs574331649	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55991325	TACTTCTCTCTTTCT[C/G]TGGTCCACTTGTGCC	4067
rs574340196	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55928391	CCTCAGGTGATCCGC[C/T]GACCTTGGCCTCCCA	4067
rs574370808	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55991700	AGCTTCAGGCACAGG[C/T]GTTTTCAGGAAACAA	4067
rs574394711	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55928605	TATTATTGATTTTAA[C/G]AGTTCTTTGTCTATT	4067
rs574399730	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55899475	TAACATAAATGTAAA[C/T]GCAGGAATAAGACCA	4067
rs574409284	snp	A/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:56007219	CAATTGCTATTTATA[A/T]CATACTGGATGTTAG	4067
rs574464377	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55980618	TTGGATTTTGGATAA[A/G]CACTAGCTTTTAACA	4067
rs574501480	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55983167	TCATGAACCCCGACA[C/T]GTGCCCAGTCTGCTC	4067
rs574506758	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:56001363	AGAGACTTACTGGCC[A/G]TGTAAGAGCAGCCCC	4067
rs574528307	in-del	-/C	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55892373	TGCATTGAGCTGAGA[-/C]CACGCCGTTGGACTC	4067
rs574547922	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55901220	TCTGAATAGTTCTCC[A/G]ATTAGAATAGCAGTT	4067
rs574554720	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55973233	ACGTGACAGCCTCAC[A/G]GTTCATGTGAGAGCT	4067
rs574594036	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55975366	GGGAAAATCACTTTG[C/T]GGGCACCAGTGTCCT	4067
rs574599056	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55892380	AGCTGAGACCACGCC[A/G]TTGGACTCCTGCCTG	4067
rs574609061	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55895535	TGGCTCACACCTGTA[A/G]TCACAGCACTTGGGG	4067
rs574618182	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55902299	AGGCGTGAGCCATTG[C/T]GCCTGGCCGTAACAG	4067
rs574670384	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55986887	TGTGCCACTACACCC[A/G]GCTAATTTTTAATTT	4067
rs574721067	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55895917	CACTCCCTACTCATG[A/G]TACCCCTGGCCTGTT	4067
rs574721526	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55999880	GGAGGCTGAGACAGG[A/T]GAATTGCTTGAACCC	4067
rs574735117	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55999355	AAGTATGGGGTCACA[C/T]GTTCATGACTTTTTT	4067
rs574735566	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55890928	GAGATAAGGTTTTGC[A/C]ATGTTGTCCAGGCTA	4067
rs574753150	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55913243	GAAATATAAATAGTT[G/T]TAAAGTTTGCTATGT	4067
rs574775550	in-del	-/CTT			intron-variant	LYN	GRCh38.p7	8:56008564	TGAAGGATTAATCTC[-/CTT]TATCATGCAGGAAAA	4067
rs574775817	in-del	-/AGAT			intron-variant	LYN	GRCh38.p7	8:56006936	TCCTTGTACATAAAA[-/AGAT]AGATAGGCTTCAGAT	4067
rs574803035	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55896982	TGACCTTAGGTGATC[C/T]GCCTGCCTTGGCCTC	4067
rs574803986	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55986257	TGGCATCCTAGTGAC[A/T]TTACAAATAGCAGCC	4067
rs574892092	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55910634	TGGTATTTGTGCTCT[C/T]TTTTGGTTCCATATG	4067
rs574896615	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55933999	TTGGGAGGCCAAGGC[A/G]GGCGGATCACAAGGT	4067
rs574899072	snp	C/T	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55927817	CCCCTGCCTGGGTGA[C/T]AGAGCGAGACTCTGT	4067
rs574912903	snp	C/T	0.00279162	0.0372561	intron-variant	LYN	GRCh38.p7	8:55979850	ATGCCACAGCATCTC[C/T]GGGGCTGCCAGAGGG	4067
rs574961551	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55947253	AGACTCCGTCTCAAA[A/G]GAGAAAAACCAAAAT	4067
rs574992615	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55887901	AGGCATAAGTCATTG[C/T]GCCTGGCTCCTTATA	4067
rs575001244	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55934311	TAAGTTTGCCAACAG[G/T]GTTTGAATCTTTTCA	4067
rs575010862	in-del	-/A/AA			intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55922765	GAGCGAAATTCCATC[-/A/AA]AAAAAAAAAAAAGAA	4067
rs575016784	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55980611	GTCAAATTTGGATTT[C/T]GGATAAACACTAGCT	4067
rs575024402	snp	C/G	1.65734e-05	0.00287862	intron-variant	LYN	GRCh38.p7	8:55947752	AGCACGCCACGGCTG[C/G]TCGTTTCCTCAGGCC	4067
rs575049112	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55974929	TTTGCGGTTTAACCA[A/G]GAGGCCAGATCCGCT	4067
rs575068267	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55889626	CTGTTCTCTCTGGAT[C/T]GTTCACAAACCAGAA	4067
rs575113953	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55927895	TGCAGGTTTTTGTGT[G/T]TACATACGTTTTCAA	4067
rs575123684	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55934284	AAGATAAAAAGAAGT[C/T]GGCAAACAGCTTAAG	4067
rs575137572	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55974597	TGAAACTCACCAGTA[C/T]GTTGGTCGTAAATCA	4067
rs575137899	snp	A/C	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55920792	TTCCCCACCACCCCC[A/C]CACCGGGTTCCAGCA	4067
rs575164592	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55967451	TCCCTAGTAGCTGGG[A/C]CTACAGGCACGTGCC	4067
rs575166959	snp	A/C	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55889469	CAGCCTCCCAAAGTG[A/C]TGTGCTGGGATTACA	4067
rs575170914	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55949337	TGTACCAACTCTTCT[C/T]TGTGCACCCCTGATC	4067
rs575223573	snp	A/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	LYN	GRCh38.p7	8:55968292	ACAGAGTCTCACTCT[A/G]TCACCCAGGCTGGAG	4067
rs575264972	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55921136	GAGTTAACATTTATT[A/T]ATCATCTATTATAAA	4067
rs575277133	snp	A/C	3.30126e-05	0.00406266	intron-variant	LYN	GRCh38.p7	8:55998510	GGAAGGTATGTTGCA[A/C]TAATGATCTTTAGAT	4067
rs575307652	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55905719	GGAGCAGGGAGAGCC[A/T]CACTCCTCTCCCATC	4067
rs575308934	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55961116	TGCCTTGAGATTAAT[C/T]ACCAACCCACTTCCA	4067
rs575318997	snp	G/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:56006459	GTGGTACAGCTGTGC[G/T]CCTCCCTGTCACTAG	4067
rs575320479	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55961926	ACAGCTATTCCGACC[G/T]TCCTGATGGTTTTCT	4067
rs575346112	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55974400	TATTAAATTTAAAGC[C/T]ACATTTTAAGGTGGA	4067
rs575373670	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55997054	TAATCCCAGCTACTC[A/G]GGAGGCTGAGGAAGG	4067
rs575375236	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55914088	GAATGGAGAGGTGGA[A/G]GGTTGTTGTTGGTGT	4067
rs575384369	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55930038	GGCGTGAACCCCATC[A/G]TGAACTGCACATGTG	4067
rs575387967	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55883520	TATACTGGCTGCTGT[A/C]CGAGCAGCCCTAGTG	4067
rs575393324	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55993820	CAACACAACAATCTT[C/G]TGAATCAAACACATC	4067
rs575401447	snp	A/G	0.00199481	0.0315187	intron-variant	LYN	GRCh38.p7	8:55908300	CCCAGGCTGGAGTGC[A/G]GTGGTGCAATCTCGA	4067
rs575416984	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55998779	TCAGCAAGATGATTC[C/T]TGTTTATTTTGTATT	4067
rs575418526	snp	A/G	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55906327	TGAGGCCAAGAATTC[A/G]TTTTTTTTGTTTTGT	4067
rs575423561	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55883256	ATCATTAAGTTGCAG[A/G]CCATCTGTGCTTAAA	4067
rs575471218	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55904322	GATGGAATGAAAATA[A/G]ATTTCTTAGAATATG	4067
rs575480602	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55901167	TTTTTTTTCCCTCTC[C/T]TTCCCCCCGTAATAC	4067
rs575480641	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55906985	AAGGATCAGGGAGAC[A/G]AGTATAAACAGGTAT	4067
rs575496115	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55982678	CCAGCACAGCCCTGT[C/T]ATCATTCCATCATTT	4067
rs575511044	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55926014	CTTGTTTTATAAAAA[A/T]TAAATTATAAGCATT	4067
rs575535217	snp	C/T	0.00279162	0.0372561	intron-variant	LYN	GRCh38.p7	8:55972549	CGTCCGCCTGGGATG[C/T]CCTCACTGATGACCA	4067
rs575549047	snp	A/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55907445	GGAGCACCATGGGCC[A/T]GTGAGGTGTCAAGGA	4067
rs575562162	snp	A/G	0.00159617	0.0282053	intron-variant	LYN	GRCh38.p7	8:55933954	GAGCTTTGGCCAGGC[A/G]CAGTGGCTCACACCT	4067
rs575574795	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55919818	CGTGCATTGGCTGAG[A/G]TGTGAGGCTCGGGAA	4067
rs575581008	snp	A/T	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55940739	TGTCTGATTCAAATG[A/T]TCAAAATCACCTTTG	4067
rs575589014	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56002244	CTAATATGGTGAAAC[A/C]CCATCTCTACTAAAA	4067
rs575603631	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55912500	GAGGTCGAGGCAAGC[A/G]GATCACCTGAGGTCC	4067
rs575677961	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55959349	GTTCTTTACTTGATT[A/T]ACTAATAACGTTTTA	4067
rs575679151	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55996274	GGTGAGGCCAGGGAT[G/T]GGCCTAGAGGGGAAG	4067
rs575683141	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55903253	CCACCTCAGCCTCCC[A/G]AAGTGCTGGGATTAC	4067
rs575708792	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55938903	GCGCGAGTCTTTTAA[C/T]CTTTCTGAGCCTCAG	4067
rs575731205	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55985564	CAGGCGCTGTCTTTA[C/T]ACAGGAATTCTTTTC	4067
rs575747257	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55897700	GAAGATCACTTGAGC[A/G]CAGAAGTTTGAGACC	4067
rs575762972	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55992980	AGGGACACATTCAGA[C/T]CATAGCATCATGCAT	4067
rs575780285	snp	A/G	0.0182019	0.0936463	intron-variant	LYN	GRCh38.p7	8:55944065	CTGCACTCCAGCCTG[A/G]GTTACAGAGCGAGAG	4067
rs575797650	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55894833	AGCCACCATGCCTGG[C/T]CTGCCTGGCTAATTT	4067
rs575839293	snp	A/C	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55986179	CAAAAAAAAAATCCA[A/C]CAGAATCCCCCCCGC	4067
rs575852700	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55953254	TTATTAAGTGTGACA[A/G]TCTGGCAGCCTGTGG	4067
rs575857926	snp	C/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55898199	ACCTGTTGTCTGTCC[C/G]CATTGTTTTGTGTTT	4067
rs575905069	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55884778	TTTAGAAGAGCAAGT[G/T]TAAATACTTGGGATG	4067
rs575927682	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55916331	CTGACAAGGCTGTTT[C/G]CTATTACCTACTGTT	4067
rs575978147	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55959616	TTTTAATTTTTTTTA[C/T]TTTGAGATAATTGTG	4067
rs576027571	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55980528	ACAGGCATACACCAT[C/T]GTGCCCCACAGTTGC	4067
rs576029607	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55973735	CGGTATCTCTGAAGT[A/G]CAAAAATTACTAAAA	4067
rs576070399	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55989367	AAAGAAGTCCATCTG[A/G]TATATTACCTAGGGC	4067
rs576072047	snp	A/G	0.0023933	0.0345097	intron-variant	LYN	GRCh38.p7	8:55932643	CCAGGCTGGTCTCGA[A/G]CTCCTAACCTCAGGT	4067
rs576081674	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55975107	CATAGAGGAATCTGA[A/G]CCGGGTGCCGCTGTG	4067
rs576126524	snp	A/C	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55990132	TAGTCCCAGCTACTC[A/C]GGAGACTGAGGCAGG	4067
rs576153810	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55884215	AGCAATCCTCCCTGC[C/T]TCAGCCTTCTGAGTA	4067
rs576165703	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55982734	GGCTTCTCTGTGTCT[G/T]GACTTCCTCCCCTCC	4067
rs576190751	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55949957	AGCCCTAGGAAACCA[C/T]GAATCTACTTTTTAT	4067
rs576199978	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55983163	AGCCTCATGAACCCC[A/G]ACATGTGCCCAGTCT	4067
rs576220810	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55911130	ACGTATATATATACA[C/T]ATACATATATATACG	4067
rs576235921	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55987242	ACATGATGAAACACC[A/G]TCTCTACTAAAATAA	4067
rs576246376	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55892547	CATAATAAGAAAGTA[A/T]CTTTCTTTTTTTTGA	4067
rs576253860	snp	C/T	1.64789e-05	0.0028704	missense	LYN	GRCh38.p7	8:55950551	TCAACACCTTAGAAA[C/T]AGAAGAGTGAGTCCT	4067
rs576341472	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55877968	CCTTCCCAAAAGGAG[C/T]TTACCAGTAGTTGAG	4067
rs576345159	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55941215	CAGATTGGATGTGTC[A/G]TTTGTCTTCAGGGTA	4067
rs576382192	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55942207	ATTAAAAGGGCCTTT[G/T]GTCACATTCTTTTGT	4067
rs576382993	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55946884	TTAGCCTGATGTCCT[C/T]AAGGTTCATCCATGC	4067
rs576399656	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55935030	ACACCATGGACGGAA[A/G]CAGCTCCACGGGCCA	4067
rs576409939	snp	A/C	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55896497	CATCACACACCGGGG[A/C]CTGTCGGGGGGTGGG	4067
rs576416934	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55982023	GCAGGGCCTCTCGTG[G/T]CCTCTCCCTGGGCGC	4067
rs576447500	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55985320	ACCCACCTGCTCTTG[C/T]CCCCACATCCTTAGG	4067
rs576484628	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55891026	GAACCACCGTGCCCA[A/G]CCATACAATGGAATG	4067
rs576488690	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55935399	GTTTGAAAATAATGA[A/C]CATGGTATGTAAGGC	4067
rs576504037	snp	A/C	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55909165	AGTAGGAAACCCTGA[A/C]CCAGAAGCAGGTGGG	4067
rs576510629	snp	G/T	0.0379877	0.132479	intron-variant	LYN	GRCh38.p7	8:56002188	TTGGGAGGCCCACTT[G/T]GTGGGCGGATCACAA	4067
rs576566110	snp	A/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55896940	AGACGGGGTTTTGCC[A/T]TGTTGGCCAGGTTAA	4067
rs576572078	snp	A/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55983365	TCAAGACACTGTTCT[A/T]GAAATTCCGCATTAG	4067
rs576597175	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55884542	GTTCACTGCACCTCC[A/C]TCTCCTGGATTCAAG	4067
rs576614323	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55902906	CAGGCTGGAGTGCAG[C/T]GGCGCAATCTCCACT	4067
rs576615793	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55986319	GAGATTTCCAGTTTC[C/T]CCACATCCTCACTAA	4067
rs576637730	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55928529	CCATCTGTAGCTCTT[C/T]TTTGGTGAGGTGTCT	4067
rs576670791	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55962816	GTTCTTCAGATTTTA[C/T]AAGAAGCATGGCACC	4067
rs576675402	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55903191	AGAGACGGGATTTCA[C/T]CATGTTGGCCAGGCT	4067
rs576684032	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56008715	CAGGCCTTTTGCAGA[A/G]CTCTAGAGGAGTAAT	4067
rs576700984	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55929243	TGAGAAGCAGGGATC[C/T]GTAGAATAGATCCTT	4067
rs576720591	snp	A/T	0.00199481	0.0315187	upstream-variant-2KB	LYN	GRCh38.p7	8:55877260	TTTATTTTTATTTTT[A/T]TTTTTTTTAATTTTT	4067
rs576750409	snp	A/C	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55986654	CTAAGCTTGGATATG[A/C]CAAACACTGCCTCAT	4067
rs576757046	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55923215	TTGAAACGAATTGGG[G/T]GTGGCCTCTAAGGTA	4067
rs576757722	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55935918	CTGTTGAGGCTGCCA[A/G]CCAGGCTATTGTGTC	4067
rs576778418	snp	C/T	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55923794	ATTTGCCTACCTCGG[C/T]CTCCCAATTGTTGGG	4067
rs576850028	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55995167	CCTGAACTTCCTGAC[A/G]CCCTCACCATGCCAC	4067
rs576879055	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55962686	ATATACGATCATTTA[C/T]CCATTTATTTCACCA	4067
rs576882237	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55914735	AAAACAGTTTCACTA[C/T]AATATCCAGTAGATT	4067
rs576886965	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55987621	GGGTTTCACCACATT[A/G]GGCAGGCTGGTCTCG	4067
rs576886994	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55980831	AGTTTATGGTTGTTG[A/G]CAGTAAGAACATTCA	4067
rs576906022	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55983406	CACTTCTGCACTTCC[C/T]ATAGGAATCAAAGTA	4067
rs576915090	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55949319	TGTGAGATGGGAGCC[A/C]TTTGTACCAACTCTT	4067
rs576925148	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55942451	TGTGTGTGTATATAT[A/G]TATATATACACACAT	4067
rs576928366	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55995864	AGTGAAATACTGGAC[C/T]GAATAGTCTTTGAGA	4067
rs576935366	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55988913	AAACAAAAAACTCAC[C/G]GAGCAAGATAGCCTT	4067
rs576963127	snp	C/T			intron-variant	LYN	GRCh38.p7	8:56003089	TTTTGAGACAGAATC[C/T]CGCTCTGTTGCCCAG	4067
rs576997159	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55955686	CAATCACTCTTCATT[C/T]GCCCCACCCTCAGCC	4067
rs577004151	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55975759	TCTGAAAAAGCCAAA[A/G]GAATAGGAAACTGTC	4067
rs577014755	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55897036	TGAGCCACTGCACCC[A/G]GCCTAAACTTCATTT	4067
rs577023913	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55897508	CAAATTTGCCTTTTC[C/T]ACCTCAATTTCTCCT	4067
rs577056440	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55890450	AGTGGTGCCAAGGAT[A/G]TGGAGAAATTGGAAT	4067
rs577058987	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55956511	TTAAATGGATCATTT[A/C]AATTTAGTTTCTCCG	4067
rs577104162	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55929284	CTTCCATCTTTACTG[A/C]GTGAGATTAGTGAGA	4067
rs577137591	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55884489	AGAGACAGAGTTCGC[C/T]CTTGTCACCCAGGCT	4067
rs577137596	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56007332	AGAGCCAGAGCAATG[A/C]TGAGGCCATATCATT	4067
rs577167806	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55982646	TGCTGTGGTCAGCTC[C/T]GGCTGGCTTGCTGTT	4067
rs577202766	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55982826	TCATTTGATCGTTTC[C/T]ACTTCAGCCATTGCC	4067
rs577224596	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55902194	TGTATTTTTAGTAGA[A/G]ACAGGGTTTCTACAT	4067
rs577225292	snp	A/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55895997	TTTGGTGTACATACC[A/T]GGTGCACTTTCATTC	4067
rs577232959	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55976451	TTGGCTTGCTCTCCC[C/T]GAGCCCCCTCACCCT	4067
rs577264355	snp	C/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55984047	GTCTTGTTGACCGCA[C/G]TGCTCCTCTTCCCAC	4067
rs577273102	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55902220	TACATGTTGGTCAGG[C/T]TGGTCTCGAACTCCC	4067
rs577277357	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55977625	TTCTAGCCCAGAGCT[C/T]ATCTCTGTCTGGCAC	4067
rs577290597	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55974636	GGGTCTAGAGGGGGA[A/G]GTTCTTGGGAAGTTT	4067
rs577377928	snp	A/C			intron-variant	LYN	GRCh38.p7	8:56009038	AACCAATTTGTTGGG[A/C]TGACTTAAGGGTGCT	4067
rs577404028	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55974989	GTGGAAATTCTCATA[C/T]ATGACTCTTACTGAG	4067
rs577404512	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55894723	TATTTTTAGTAGAGA[C/T]GGGGTTTTGCCGTGT	4067
rs577458637	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55934460	TTCTCTCCATATTCT[A/G]TGTATGCCGTTCACC	4067
rs577465223	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55975483	CTATCTATGTGAATC[A/G]TCACCAAAAGTTGCA	4067
rs577465634	in-del	-/A			intron-variant	LYN	GRCh38.p7	8:55916189	AGATGATCATTGGCT[-/A]AAAAAAAATGGTGGT	4067
rs577465999	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55969354	AGTGAGCCTGGCCAA[A/G]TGTCTGCAGAGGGCA	4067
rs577500337	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55922423	CCTGGTTCTATGTGT[A/G]CCAGTGTATTAATTT	4067
rs577512685	in-del	-/A	0.0138799	0.0821421	intron-variant	LYN	GRCh38.p7	8:55929041	CAGTACCACTTATTG[-/A]AAAAAAATATCCTTT	4067
rs577528095	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55937644	GTAAGGCATTGCTAG[A/G]TTTTATGAAACCAAA	4067
rs577536418	snp	C/T	0.00478085	0.0486577	intron-variant	LYN	GRCh38.p7	8:56004223	AGGTGTGAGTCACCG[C/T]ACCCGGCCTAAATAT	4067
rs577571142	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55936394	CCTATAATCCCAGCA[C/T]TTTGGGAGGCTCACG	4067
rs577572996	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55930002	TCCTGTCAGATCAGC[A/G]CCATAGTAGATTCTC	4067
rs577586099	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55945488	CTGAAATGGAGATTT[G/T]ATGGGCTTTCATCAG	4067
rs577619728	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55962054	TTATACCAAATGTGC[C/T]CTTTTACGTCTTGCC	4067
rs577620396	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55936315	GAGCTTCCTCCACAG[A/G]AAGGCAGCAAGACCT	4067
rs577625945	snp	A/C	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55893489	TGTTAAGGAACACAG[A/C]ACCTTTGTTACTGAC	4067
rs577646036	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55929100	AAAGATCAGTTGACT[A/G]TATTTGTGTGGTTCT	4067
rs577680347	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55896832	CAACCTCTGCCTTCC[A/G]GGTTCAAGCAATTCT	4067
rs577700150	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55937856	GGGTGCCACCACACC[C/T]GGCTAATTTTTGTGT	4067
rs577843323	snp	A/C	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55931952	AAAAAATAAAATTTA[A/C]ATTTATAAGCCTCAA	4067
rs577863466	snp	C/T	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55972796	CCAACCTTTTCTATA[C/T]CTTCCCCCCACTTTA	4067
rs577875611	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55966391	TTTTTTAATTGAGAC[A/G]GAGTCGCACTCTGTC	4067
rs577891141	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	LYN	GRCh38.p7	8:56012046	TGTTTTGCTTCTCCC[A/G]GTTCCTCCTCTTCTT	4067
rs577904687	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55932640	TGGCCAGGCTGGTCT[C/T]GAACTCCTAACCTCA	4067
rs577931003	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55895649	TTTTTAAAGGAATTG[A/G]CTTCTAGTCAATGCT	4067
rs577961911	snp	A/G	0.00478085	0.0486577	intron-variant	LYN	GRCh38.p7	8:55951184	GGGAAGGGAGGCTGC[A/G]GTGAGCCGTGATCAC	4067
rs577996944	snp	G/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55892489	GATTTGATGATACAG[G/T]TATATTAATATTTCT	4067
rs578007602	snp	A/G	0.00438332	0.0466095	intron-variant	LYN	GRCh38.p7	8:55958775	AGGTTTATCTATGTC[A/G]TAGCATGTGTCAGAA	4067
rs578007931	in-del	-/C			intron-variant	LYN	GRCh38.p7	8:55901456	GCCAGGCTTTAGACT[-/C]CTTCTTGGGCTCATG	4067
rs578031463	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55921985	CTTACAGTAACAGAG[A/G]AGCGATGGACAGATG	4067
rs578032613	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55970961	TCACATGCTTGGCAC[A/G]GACACAAGCACCTCA	4067
rs578060714	snp	A/C	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55924470	TGGGTTCAAGTAATT[A/C]TCCTGCCTCAGCCTC	4067
rs578096855	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:55977013	AACATGGTGAAACCC[A/G]GTCTCTACTAAAAAT	4067
rs578129135	snp	A/G	0.000798403	0.0199641	intron-variant	LYN	GRCh38.p7	8:55885963	AGTGAGGGGTGGGGC[A/G]GGGTGGGAGAGAGGA	4067
rs578130378	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55917927	TGTTGTATTCATAGA[A/G]GTTCTTTGGGTTTCT	4067
rs578139025	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55966174	AGTGCCAATAAAAAC[A/G]TTTTTTTGCTACTAT	4067
rs578155455	snp	C/T	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:55997044	TGCGTGCCTGTAATC[C/T]CAGCTACTCGGGAGG	4067
rs578155814	snp	A/G	0.00119737	0.0244387	intron-variant	LYN	GRCh38.p7	8:56009723	AATTCTGAGGTGTAC[A/G]CGGGGTTAGGACTTC	4067
rs578156645	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55879090	ATGAGCTTGAGCACG[C/T]GGTCACACATTCTTT	4067
rs578182656	snp	A/G	0.000399281	0.0141238	intron-variant	LYN	GRCh38.p7	8:56003040	TTTACGCAGTAAACT[A/G]CTGGCTATGTTTTTG	4067
rs578242617	snp	C/T	0.499946	0.00519141	intron-variant	LYN	GRCh38.p7	8:55911210	ACACATATATATATA[C/T]ACGTGTATATATATA	4067
rs745313839	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55980937	CAATGCCAGCTCCCC[A/G]CGGCCGCTTGCTAGC	4067
rs745331070	snp	A/G			upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55878147	ATGGGACATTAAGAA[A/G]GAAAGACAGATATGG	4067
rs745400667	snp	A/G			utr-variant-5-prime	LYN	GRCh38.p7	8:55877398	CCACTGAGCTCAGTC[A/G]CTTGGGGGCCATTTT	4067
rs745414148	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55915534	ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA	4067
rs745429164	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55982523	TTCCATTTCCAGACC[A/T]TCTACCTCCCCCACC	4067
rs745477697	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55993297	AACCAGAACTTGGCC[C/T]GGGGAGAGCTTGTGA	4067
rs745504456	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55955645	ATGTTTTTATCATCC[C/T]GAAAGGAAACAATGT	4067
rs745510506	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55966518	GATTACAGGCGCCTG[C/T]CACCACACCCAGCTA	4067
rs745512037	snp	G/T			intron-variant	LYN	GRCh38.p7	8:56006488	AGCTATCTGTTCCTT[G/T]TCTCTACTGTACCAC	4067
rs745525931	snp	A/C	3.2956e-05	0.00405918	missense	LYN	GRCh38.p7	8:55952005	ACTTTGACCCTGTGC[A/C]TGGTGATGTTATTAA	4067
rs745527308	snp	C/T	1.65034e-05	0.00287253	synonymous-codon	LYN	GRCh38.p7	8:56009937	GACGTGATGACCGCC[C/T]TGTCCCAGGGCTACA	4067
rs745537489	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55977808	CCTGTAATCCCAGCT[A/G]CTCAGGAGGCTGAGA	4067
rs745595320	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55962830	ATAAGAAGCATGGCA[C/T]CTGTCTCTGCTTCTG	4067
rs745604407	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55942153	ATCCTTTGAAGAATG[C/T]ATAAATATTTTAGGG	4067
rs745629810	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55885351	TTTCCTTTCTACAGT[C/T]CATGCTTCAGGCAAA	4067
rs745631117	snp	G/T			missense	LYN	GRCh38.p7	8:55966843	CTCGTGAGGCTCTAC[G/T]CTGTGGTCACCAGGG	4067
rs745661836	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55911527	ATGACTCTCCTGGTG[A/G]CCCTGAACTCGTAGG	4067
rs745674219	snp	A/G			intron-variant	LYN	GRCh38.p7	8:56001746	AAGATTATATAGTCA[A/G]ATTATGTATATAATC	4067
rs745698246	snp	C/T	0.000122972	0.00784034	intron-variant	LYN	GRCh38.p7	8:56009868	TGCCAGGTTTCTAAA[C/T]GGCATGGGTTTCTGT	4067
rs745702419	snp	A/T			intron-variant	LYN	GRCh38.p7	8:56002831	TTTTTTAGTCACGAG[A/T]GTTGTATGTTACGAG	4067
rs745719424	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55944888	TGTTCAAAATAAAGG[A/G]GATTAAAAATCAAGT	4067
rs745720511	in-del	-/T			intron-variant	LYN	GRCh38.p7	8:55988538	TTATGTGAATTCTTC[-/T]TTTTCTCAAGCATAG	4067
rs745731569	snp	A/T			intron-variant	LYN	GRCh38.p7	8:56003732	AAAATAAAAAGGAAA[A/T]AAAAGAAAGGAGGAA	4067
rs745752181	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55934220	GACAGAGCGAGATCC[A/G]TCTCAAAAAAAAAGA	4067
rs745775449	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55971959	CAGGGGGCTTCAGTT[C/G]ACTCTCCTGTCAACT	4067
rs745784439	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55983471	ACCTCAGCCTCCAGG[C/T]GTCTCCTCCCCCTGA	4067
rs745804098	snp	C/T	1.67466e-05	0.00289362	intron-variant	LYN	GRCh38.p7	8:55966908	CAAGGGTGAGTTCCT[C/T]CCACTGCCCAGAGCT	4067
rs745807846	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55945211	ACATGTGTTTCGGTC[A/T]TATAAAAAGCATATT	4067
rs745809537	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55933304	TGAAAACCCTCACAG[A/G]ACTGGCTTTGGTGAT	4067
rs745815088	snp	A/G	3.32762e-05	0.00407885	missense	LYN	GRCh38.p7	8:55946448	AATATTCTCTCGTAG[A/G]TTCCAGAATCTCAGC	4067
rs745872883	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55970736	TAGGGCTGGACACAG[A/G]TTCTGTAATAGAGCA	4067
rs745906314	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55987373	AGATCAGGCACTACA[C/T]TCCAGCTTGGGCTAC	4067
rs745955789	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55919809	GCAGTTGAACGTGCA[C/T]TGGCTGAGGTGTGAG	4067
rs745975290	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55918421	TCTGGGCTATGGAGC[C/G]GGGACATTTGCATTT	4067
rs745995234	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55990043	CAGGAGTTTGAGACC[A/T]GCCTGGCCAACATGG	4067
rs746004856	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55999150	TGAGCAAATATTTTT[G/T]CAGTGCTCACTGTCT	4067
rs746005069	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55962973	TCTCTTGTGAACTAA[C/T]AGAGCGAGAACTCAC	4067
rs746010698	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55902478	AATTACAGGTGCGCT[C/G]CACAACGCCCAGCTA	4067
rs746011702	in-del	-/A			intron-variant	LYN	GRCh38.p7	8:55953544	TCCCAGTTACTTTGG[-/A]GGCTGAGGCAGAAGA	4067
rs746016465	snp	G/T			utr-variant-3-prime	LYN	GRCh38.p7	8:56010984	ACTAAGATTCTAATC[G/T]CTGAAGAACCTTATA	4067
rs746027645	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55892274	AAAAATCCAAAAATA[A/G]CCAGGTGTGGTGGCA	4067
rs746047026	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55980383	AACCAACCTAGAGGT[C/G]CTCCACTCCCAGGAG	4067
rs746048108	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55941487	GCCCATTTCAACTCA[C/T]AGAGCATTTCCTTTA	4067
rs746073795	snp	A/C	8.31608e-05	0.00644775	intron-variant	LYN	GRCh38.p7	8:55950455	ATGTGTATTTCTATT[A/C]TAGGCATGGAGAATG	4067
rs746077693	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55927001	ACTGACTTCCCACCC[C/T]CAACCAGCTTATTAT	4067
rs746103346	snp	A/G			downstream-variant-500B	LYN	GRCh38.p7	8:56012590	TAAGTGTGGTGGCAC[A/G]TACCTATGGTCCCAG	4067
rs746171622	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55916015	TTTAAAGGGTAGCCA[C/T]TGTTTTAAAAGCATA	4067
rs746242409	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55938093	TAATATTCTAAGGCT[C/T]TTGAATGAGGATGAG	4067
rs746249590	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55896985	CCTTAGGTGATCCGC[A/C]TGCCTTGGCCTCCCA	4067
rs746272399	snp	C/T			intron-variant	LYN	GRCh38.p7	8:56006947	TAAAAAGATAGGCTT[C/T]AGATTCCCTTCTTCC	4067
rs746274497	snp	A/G	1.64887e-05	0.00287125	missense	LYN	GRCh38.p7	8:55998385	GAGCGGAAGAACTAC[A/G]TTCACCGGGACCTGC	4067
rs746280840	in-del	-/TT			intron-variant	LYN	GRCh38.p7	8:55890729	TATGTACATTGGAAT[-/TT]TTTTTTTTTTTTTTT	4067
rs746284266	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55965378	GGGTGGGGGAGGAGT[A/G]GAGGGAGTGGCTCCC	4067
rs746293255	in-del	-/TATGA	1.71911e-05	0.00293177	intron-variant	LYN	GRCh38.p7	8:55952158	ACAAGATATATTTGT[-/TATGA]TATGTATAAGACGTC	4067
rs746298052	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55976481	TCTTGGTGTGGCCCG[C/T]TCCCTTTCACTCACA	4067
rs746319786	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55907857	GGTGACAGAGTGAGA[A/C]CCTGTTTCACATAAA	4067
rs746383982	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55987565	GGGATTATGGGTGCC[C/T]GCCACCACACCTAGC	4067
rs746401706	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55948497	GGACGCCTGAGTGTC[A/G]TCATCTCCTCAACCC	4067
rs746411453	in-del	-/ATTT			intron-variant	LYN	GRCh38.p7	8:55908230	TTAAACCATTTATTT[-/ATTT]ATTTATTTATTTATT	4067
rs746433259	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55882808	GATTCAGGGGGTTGT[C/T]TAAGGTCACAGGCTT	4067
rs746459348	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55888964	TATTATTTCAAATTT[A/G]ATAGATGCCCAATGT	4067
rs746478222	snp	G/T			upstream-variant-2KB	LYN	GRCh38.p7	8:55876682	AGGTCTGTGGCCAAG[G/T]TGGCAAGAGTTAGGT	4067
rs746551996	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55993018	GGGGGTAAGATTGCC[A/C]CCAAGGGAGCAAAAA	4067
rs746565506	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55913423	GGCCCAAGAATCTAT[A/G]TTTTTAACAAATACT	4067
rs746567853	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55977514	TTTCATGCTCCTAAC[A/G]TTTTGTTTTATTACT	4067
rs746614433	snp	C/G			intron-variant	LYN	GRCh38.p7	8:56005458	CTGCCCTCGGCGCTG[C/G]CCTCCCTCCCTCATG	4067
rs746618797	in-del	-/TTC			intron-variant	LYN	GRCh38.p7	8:55990805	ACTAGTTTTTCAGGT[-/TTC]TTTGAAATCCCCTGG	4067
rs746642959	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55974804	TTGATTAGTAACAAC[C/T]TTTGATTGATAGCGT	4067
rs746673798	snp	C/T	3.43613e-05	0.00414481	intron-variant	LYN	GRCh38.p7	8:55953794	GTAAAGTACAAAGTA[C/T]TGCATTTCTTAACCT	4067
rs746741416	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55898122	AGAAAAGTTCTGTGA[C/T]ACCCTCCCCCCAAAA	4067
rs746786324	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55883093	CAAAATCATCTGACA[C/T]AAAGCCCATTTGATA	4067
rs746806908	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55921192	AAATATATTCTATTA[C/T]GGAATTGCTGCTGAC	4067
rs746849670	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55887705	ACCTCCACCTCCCGG[C/G]TTCAAGTGATTCCTG	4067
rs746874463	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55971889	GACCTTCATAGCTTA[C/T]GAGGAAGATTACCAC	4067
rs746890563	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55960711	AATTAAAATTCTATC[A/G]CTGTTAACCCAGTAA	4067
rs746893716	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55928347	GATGGGGTTTCACCA[C/T]GTTGGCCAGGCTGGT	4067
rs746909402	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55981541	TTTTTTTTAATATAG[A/G]GATAGGGTCTCACTA	4067
rs746923187	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55943689	TTCTGCCTGCCCTCC[C/T]CTCAATATGTCCCCA	4067
rs746942159	snp	C/T	4.95503e-05	0.00497722	intron-variant	LYN	GRCh38.p7	8:55947732	TGGAGGAGTAAGTGC[C/T]CTCAAGCACGCCACG	4067
rs746963355	snp	C/T	3.2963e-05	0.00405961	synonymous-codon	LYN	GRCh38.p7	8:56009972	GCCCCGTGTGGAGAA[C/T]TGCCCAGATGAGCTC	4067
rs746994423	snp	G/T			utr-variant-5-prime	LYN	GRCh38.p7	8:55877368	CTCCCAAAGTGCTGG[G/T]ATTACAGGCATGAGC	4067
rs747033224	in-del	-/A			intron-variant	LYN	GRCh38.p7	8:55947565	CCCATGAGGTTTGTT[-/A]AAACGCTTCTGCTGA	4067
rs747076938	snp	A/G			utr-variant-3-prime	LYN	GRCh38.p7	8:56010363	GCTCTGCTTGACAAC[A/G]TCTGAGTGCAGCCGT	4067
rs747168749	in-del	-/AA			intron-variant	LYN	GRCh38.p7	8:55913494	TTGAATAAAACGATT[-/AA]AGTTGTGCTTGCTGA	4067
rs747168842	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55984858	TTGCTTTCAGAAGTT[A/G]CTCCTTTTCATACAT	4067
rs747181102	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55968912	TGAAGCCATAGGAGG[C/T]TGGAGAGTTTGTTCA	4067
rs747193033	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55953003	ATGACCTGCTCGAAG[G/T]GGATGCACATTATAG	4067
rs747194684	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55977976	GGTACACTCTGAAAC[A/G]GACAGGACTTCTTCT	4067
rs747196660	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55991218	CTGTGGCCCCAAGGG[G/T]ATCTTTGTTGAAGGG	4067
rs747248869	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55972095	AACTCATGTTCACAG[A/G]TCCAGGGTCTCTTTC	4067
rs747333273	snp	C/T	1.64999e-05	0.00287222	intron-variant	LYN	GRCh38.p7	8:55950639	TCACCTTTTTCTTGC[C/T]GTGGAACATAATATG	4067
rs747351282	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55881163	ACTGTTATTTATTGC[A/C]GTGAATTCTATTCAT	4067
rs747377985	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55970239	TCACTTTCCTGCTCC[G/T]CTTCTCGCTCCTTCT	4067
rs747392020	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55974017	CTTCTGGTTGATACA[G/T]CACTTCTACCTCCAT	4067
rs747410952	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55919550	TTGAAGAAAGAATCT[A/G]TAATCCTTTTGGTCT	4067
rs747425344	in-del	-/GTA			intron-variant	LYN	GRCh38.p7	8:55995951	ATCTGCCAAATCCCT[-/GTA]GTAGTGGGCTAACAA	4067
rs747449703	snp	C/T	1.64732e-05	0.0028699	synonymous-codon	LYN	GRCh38.p7	8:55969733	CAGTTTGCTGGATTT[C/T]CTGAAGAGCGATGAA	4067
rs747463869	snp	C/T	1.64817e-05	0.00287064	synonymous-codon	LYN	GRCh38.p7	8:55998411	CCTGCGAGCAGCTAA[C/T]GTTCTGGTCTCCGAG	4067
rs747481719	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55946688	TACAACCAATACCGC[A/C]CTCCATCTCCAGAAT	4067
rs747496718	in-del	-/ACG			intron-variant	LYN	GRCh38.p7	8:55897926	CAAACAACAACAACA[-/ACG]ACAACAAAAACTTTT	4067
rs747496796	in-del	-/C			intron-variant	LYN	GRCh38.p7	8:55935686	CTCAGGAGGCTGAGG[-/C]AGGAGAATCGCTTGA	4067
rs747497800	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55934176	GGTTGCAGTGAGCCG[A/T]GATTGTGCCATTGCA	4067
rs747522540	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55998766	AACACAAATAGATTC[A/G]GCAAGATGATTCTTG	4067
rs747525732	snp	C/T	1.64855e-05	0.00287097	missense	LYN	GRCh38.p7	8:55950491	AAGCAAAGTCCCTTT[C/T]AACAAAAAAAGAAGG	4067
rs747527664	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55992480	CCCTTTCCCTCACCC[C/T]AGCTCCATATGGAGC	4067
rs747528231	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55883228	TGCTTTTGCACCATC[A/G]TAAAGTTGAAAAATC	4067
rs747560949	snp	C/T	1.6504e-05	0.00287258	intron-variant	LYN	GRCh38.p7	8:55999378	ACTTTTTTGTTTAAG[C/T]TTAAATACCCAAGTA	4067
rs747633647	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55916323	AACTGCAACTGACAA[A/G]GCTGTTTCCTATTAC	4067
rs747657747	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55936151	AGGGACGAATTCCTA[C/T]AAATGATGCTTGAAC	4067
rs747677629	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55897083	ACTGCAATGGAATGA[C/G]CTGGTTGGAGAACGA	4067
rs747731351	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55964156	AGGATGGTTTTTTTT[G/T]GTCAGCTTTATGTTA	4067
rs747740058	snp	C/T			intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55924149	GATAGCATGATCTAA[C/T]GTTGAAACAGCACTA	4067
rs747799387	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55984719	GTCAGAGCAATGCTT[C/T]GAGGCATAAATCAGA	4067
rs747815541	snp	C/G/T	8.3124e-05	0.00644639	intron-variant	LYN	GRCh38.p7	8:55946413	GTAAGAAAAGCTAAA[C/G/T]AGAATTTTTTTTTCT	4067
rs747832100	snp	C/G	1.65463e-05	0.00287626	missense, intron-variant	LYN	GRCh38.p7	8:55941926	GATTTGAAGACTCAA[C/G]CAGTACGTAATACTG	4067
rs747915261	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55984576	CTCAAAGTAGATTCA[A/C]CTTCCTAAGTCCTGC	4067
rs747938237	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55903273	GCTGGGATTACAGGC[A/G]TGAGCCACCGTGCTG	4067
rs747955170	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55893575	CAGAGAGAGGCATAA[C/T]TGACCTGTGGCATTT	4067
rs747977800	snp	A/G/T			upstream-variant-2KB	LYN	GRCh38.p7	8:55876568	ATTTAACTGGTCTAG[A/G/T]TAGGGCCTGGGCATG	4067
rs747989702	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55902586	ACATTACAATGTTTC[A/G]ATCAATATATAGCAT	4067
rs747991747	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55914192	CAGGCCAGGTCAGAG[A/G]GTTTTTAGGATGGCC	4067
rs748001021	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55981502	AGTAACTAGAAGAAC[A/G]TATTTTTTGTGTGTT	4067
rs748006077	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55958950	CTCTGAGACCTTATT[G/T]TCCATTCCTTTGAGT	4067
rs748034542	snp	A/G	4.97599e-05	0.00498773	utr-variant-3-prime	LYN	GRCh38.p7	8:56010126	AGCACAGGGAGACCC[A/G]TCCATTTGGCAGGGG	4067
rs748035706	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55992180	CCTGGGCCTGACATT[A/G]TAATGAAGAGAATCA	4067
rs748038916	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55970298	AATATTCATTTGTAC[C/T]ATTTTTAGTACTAGC	4067
rs748044630	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55913021	AAAATGACAAGTGAT[A/G]TAATAGAGTTAGTGG	4067
rs748054336	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55953286	TGTCTGTTGGCTTTG[C/T]TGTTTTTGTTCATGT	4067
rs748074374	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55924793	CATATACTGCAGATA[A/T]GTCACTTGGTAAGTC	4067
rs748079540	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55965011	TTGCAGTGACACCAG[C/T]AGCTATTACTCCCTT	4067
rs748084150	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55954311	GTGCAAGAAATTTGC[C/T]TCCATCTCTGGGAAA	4067
rs748120892	in-del	-/TTGG			intron-variant	LYN	GRCh38.p7	8:55967330	TTTTTTTTTTTTTTT[-/TTGG]AAACAGAGTCTCACA	4067
rs748124598	snp	A/G	1.65466e-05	0.00287628	missense	LYN	GRCh38.p7	8:55953837	TTCAAATTAGAGCAG[A/G]CAGATGGCTTGTGCA	4067
rs748127030	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55980903	TTTCATCTTCCCAGA[C/T]GGAAGCTCTTTGCCC	4067
rs748141799	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55887468	TTCTGTACGTCTTTA[C/T]ATTTAAAAGAATGAG	4067
rs748245269	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55895601	TCAAGACCAGGCTGG[A/G]CATCATAGTGAGACC	4067
rs748270691	snp	C/T	1.64735e-05	0.00286993	missense	LYN	GRCh38.p7	8:55969764	GGTGGCAAAGTGCTG[C/T]TTCCAAAGCTCATTG	4067
rs748272850	snp	C/T	1.64887e-05	0.00287125	intron-variant	LYN	GRCh38.p7	8:55947609	GTGTTCTCTTGTGTT[C/T]ATCTTTAGATCCAGA	4067
rs748295990	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55938367	TTATTTACTGTTCAA[A/C]AAATGGTTTTGAAGG	4067
rs748317186	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55951075	CAGCAAGACCCCATC[G/T]CTACAAGAAATACAA	4067
rs748322018	in-del	-/AG			intron-variant	LYN	GRCh38.p7	8:55936622	TCCAGCCTGGGTGAC[-/AG]AGTGAGACTCCATCT	4067
rs748329550	snp	A/G			intron-variant	LYN	GRCh38.p7	8:56007399	ACAAATCTGTCTTTC[A/G]CTTTAAGCAATGAAA	4067
rs748332966	snp	G/T			intron-variant	LYN	GRCh38.p7	8:56001463	ATCACTACTGTTTCA[G/T]GTGGGGATGAGCCAC	4067
rs748333116	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55987835	TAGGGAAATTGTAAC[C/G]TCTCCAAGACTCAGC	4067
rs748404815	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55993841	CAAACACATCCTCTT[C/T]TCATCAAGCTTGACC	4067
rs748405179	in-del	-/AT			intron-variant, downstream-variant-500B	LYN	GRCh38.p7	8:55968251	GTAACAATGCCTAAT[-/AT]ATATATATATATTTA	4067
rs748443407	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55893355	CACTGACCCACATGT[A/C]ATCAAACATCCTGTT	4067
rs748451219	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55905731	GCCTCACTCCTCTCC[C/T]ATCTGTTGGGAGAGC	4067
rs748516635	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55983799	ATGTCCCAGAACTCA[C/T]TCTTTCAACCTATTT	4067
rs748535248	snp	G/T			upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55878626	TCATTTTTCTATTTT[G/T]CTCCATAGGATTCTT	4067
rs748577057	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55957762	AGTCTGGACAACATG[G/T]TGAAACCCTGTCTCT	4067
rs748595323	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55997265	TAACCTGACAGAAAC[A/G]ACATCCTGTTCTTGA	4067
rs748606421	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55996236	GAGTAAAGGGGAGTT[C/T]AGGGAAGGCCCACGG	4067
rs748628709	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55968873	CTTAAAGTTCTAGGG[C/G]AAAAACAGGTCTTGC	4067
rs748632469	snp	A/G			utr-variant-5-prime	LYN	GRCh38.p7	8:55877768	CATCTATCCTGTCAA[A/G]GAGCCTTAATTGATT	4067
rs748665852	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55901363	TTCTCTTGTCTGATG[A/T]AGTCAGTGTAAGTGA	4067
rs748667218	in-del	-/AAT			intron-variant	LYN	GRCh38.p7	8:55993197	AATTCTTCCTGGAGG[-/AAT]AATAATGAAAAAAAA	4067
rs748668168	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55939269	GTGCCTGAGCAGTGA[C/G]GCCATGCTAATTCTC	4067
rs748687250	snp	A/T	3.30535e-05	0.00406518	intron-variant	LYN	GRCh38.p7	8:55999575	CTTAGCTATTTACAA[A/T]CAAGCTGTATAAATG	4067
rs748690972	snp	A/G	3.32458e-05	0.00407698	synonymous-codon	LYN	GRCh38.p7	8:55950780	AGAAAGTGAAACATT[A/G]AAAGGTAGGAAATTG	4067
rs748750879	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55934219	CGACAGAGCGAGATC[C/T]GTCTCAAAAAAAAAG	4067
rs748782789	in-del	-/AGG	0.00016584	0.00910454	intron-variant	LYN	GRCh38.p7	8:55954030	TCTAGAGATGGTGAC[-/AGG]AGAAGTAAAGGCTCA	4067
rs748804676	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55946346	CTTAATAAATGAGCC[C/T]ATCCTAACATCTGCT	4067
rs748806640	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55994347	GTCTTGGTGAACGCT[G/T]TAATTACTGTTTGGA	4067
rs748811132	snp	C/T			upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55879329	TTGACTCTACGTCAT[C/T]CCCTCCCCCATCAAT	4067
rs748812732	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55972950	ACCGTTGTCAATAGC[A/G]TCAGAGTTGGGAAAT	4067
rs748813566	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55885184	GTTCAGAATGCTGCT[A/C]CTTAAATGACATCCT	4067
rs748830815	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55905636	GAGGATGGATAGTTT[A/C]CCAGGGTTGGAGTCC	4067
rs748840942	snp	A/G			intron-variant	LYN	GRCh38.p7	8:56001876	GTGATTGGGCCCCTC[A/G]CTGGTGGCAAAGCTG	4067
rs748845096	snp	A/G	1.6914e-05	0.00290805	intron-variant	LYN	GRCh38.p7	8:55950811	TTCAAAGCCTCTTTT[A/G]AAACACTATTTAGGA	4067
rs748875448	snp	C/T	1.6477e-05	0.00287024	synonymous-codon	LYN	GRCh38.p7	8:55999428	CTTAGGTGCTAAGTT[C/T]CCTATTAAGTGGACG	4067
rs748883785	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55904674	AGAATTGCTTGAGCC[C/T]GGGAGGTGGAGTTTG	4067
rs748898641	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55983716	ATTTGGCTTCTGGGA[C/T]ACTGTTCTCTGCTTT	4067
rs748907503	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55995846	TCTTTGTTTCCACTC[A/G]GAAGTGAAATACTGG	4067
rs748910085	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55916669	CTCCTCCCCTGGGAG[A/T]GGAGCCAGGCTGACC	4067
rs748934215	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55945422	ATTTGAAGGATAGTA[C/T]GCAGCCATGGGTTTT	4067
rs748962366	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55983560	CTCTTGAACCTCCCA[C/T]CCCTCGACCCCAGCA	4067
rs748963497	snp	A/G	4.96134e-05	0.00498039	intron-variant	LYN	GRCh38.p7	8:55999592	AAGCTGTATAAATGA[A/G]AAAAAGTCAGGTTGC	4067
rs748968064	snp	C/T			intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55922725	TGAGCTGAGATTGTG[C/T]CACTGCACTCCAGCC	4067
rs749007515	snp	C/G			upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55878476	ATTCATCAGTAGCAG[C/G]AGAAACTTTAATGTA	4067
rs749029574	snp	G/T			intron-variant	LYN	GRCh38.p7	8:56009165	AAATATACTACAAGT[G/T]GAAGCTGAAAGCATG	4067
rs749044228	snp	A/C	1.64735e-05	0.00286993	intron-variant	LYN	GRCh38.p7	8:55946441	TCTAACAAATATTCT[A/C]TCGTAGGTTCCAGAA	4067
rs749097175	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55901791	CGGCTCCCAGCTGAA[G/T]AGCTTGTGCTGAGTC	4067
rs749116987	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55901409	GACTTTAATATGAAA[A/G]GAACTGTTTAATTGA	4067
rs749134689	in-del	-/GAGGTGTAGGA			intron-variant	LYN	GRCh38.p7	8:55914211	TTTAGGATGGCCTGT[-/GAGGTGTAGGA]GGGTCTGGAGGTCGG	4067
rs749148237	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55912235	TGTGCCCCTTTTGCA[A/G]TGTATCATTAAGGAT	4067
rs749164386	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55979331	ACAGGCGTCAGCCAC[C/T]GTGCCCAGCCTCATT	4067
rs749187073	snp	A/C/G	0.000102261	0.00714989	intron-variant	LYN	GRCh38.p7	8:55966707	CCCGCCTTCTTTTTT[A/C/G]TTCCTAGGTTACTAT	4067
rs749187406	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55955115	TCTCCAGCCCCGGCA[A/G]AACAGAAGCTGCAGC	4067
rs749224990	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55973762	AAAAATGGAACAATT[A/G]TTTGTGAGTTAAATG	4067
rs749235356	snp	A/G	1.65064e-05	0.00287279	intron-variant	LYN	GRCh38.p7	8:55953995	GATGGGTAAGTGTGC[A/G]GCTCGGGGATCTATG	4067
rs749249964	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55991409	AGTGGAGGAAGAGGC[A/C]GACACTTGGTGACTA	4067
rs749325587	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55961500	GAGATCATCTGGGAG[C/T]TGCCGCCATTCTTGG	4067
rs749330409	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55991820	AAAATGAAAAACACA[C/G]AAACAGCACAGGTAG	4067
rs749339747	snp	C/T	1.67674e-05	0.00289541	intron-variant	LYN	GRCh38.p7	8:55950441	TTAGCTTCTTTTTGA[C/T]GTGTATTTCTATTCT	4067
rs749340248	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55882928	AATGCCTCTCAACTT[A/T]TGATGAGGCTGTGTC	4067
rs749348635	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55883812	TACATTGCCTCCCAT[C/T]TTTTAAGGCTGATAA	4067
rs749422533	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55929147	TTCTATTCATATGTA[C/T]TGAGTCTTTTTGTTA	4067
rs749442547	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55984302	ACTCCGAAGCTTCTA[C/G]CTCAGCCCAAACTGC	4067
rs749442949	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55987689	CCAAAGTGCTGGGAT[C/T]ATAGGCATGAGCCAC	4067
rs749460924	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55920387	CACAGCAACATTTCT[G/T]AAGTGTGATCATGTC	4067
rs749463299	in-del	-/T/TTTTTTTTTTT			intron-variant	LYN	GRCh38.p7	8:56003062	TGTTTTTGTTTTTTG[-/T/TTTTTTTTTTT]TTTTTTTTTTTTTTT	4067
rs749469706	snp	A/G	1.64746e-05	0.00287002	intron-variant	LYN	GRCh38.p7	8:55969799	TTCTGCTCAGGTAAC[A/G]TATTCAAAAAGCCCC	4067
rs749472116	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55986392	TAGTACAGTGAGTTT[G/T]GAAATATCTATCCCA	4067
rs749474188	snp	C/G	1.65647e-05	0.00287786	intron-variant	LYN	GRCh38.p7	8:55947746	CTCTCAAGCACGCCA[C/G]GGCTGCTCGTTTCCT	4067
rs749477955	in-del	-/AAAAAAAAA			intron-variant	LYN	GRCh38.p7	8:55905410	GTGAAACTCCGTCTC[-/AAAAAAAAA]GAAAGAAAGAAAGAA	4067
rs749526062	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55990748	AAAAGGGAGAAGGGC[A/G]TAATGAGTCATGTCC	4067
rs749528754	snp	G/T			intron-variant	LYN	GRCh38.p7	8:56000586	ACAAAAAATTAGCTG[G/T]GCGTAGTGGTGGGCA	4067
rs749583582	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55967655	CATTTTCCTTTTCAG[C/G]ATTATCTAAGTGTTC	4067
rs749614039	snp	G/T			intron-variant	LYN	GRCh38.p7	8:56007929	TTTGAGACCAGCCTG[G/T]CCAACATGGTGAAAC	4067
rs749620863	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55953277	GCCTGTGGTTGTCTG[C/T]TGGCTTTGTTGTTTT	4067
rs749641128	snp	A/G			utr-variant-5-prime	LYN	GRCh38.p7	8:55877655	GATAAGTTCACAAAT[A/G]TGATATCTGCAAAAA	4067
rs749646907	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55915662	AGTGAGCTGAGATTG[G/T]GCCATTGCACTCCAG	4067
rs749652337	in-del	-/GTCTTTTTT			intron-variant	LYN	GRCh38.p7	8:55909991	TGTGTGTGTGTGTGT[-/GTCTTTTTT]TTTTTTTTTTTGAGT	4067
rs749655956	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55954295	TGGATGCACGGCTCA[A/C]GTGCAAGAAATTTGC	4067
rs749699585	snp	C/T	1.64795e-05	0.00287045	intron-variant	LYN	GRCh38.p7	8:55969682	TTTTTCTTGTGTGTT[C/T]GGAATGCACTAACTT	4067
rs749740275	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55899136	TTACTACCTGTTTTA[C/G]TTTTGTATCAGGCAA	4067
rs749791683	snp	C/T	1.64849e-05	0.00287092	missense	LYN	GRCh38.p7	8:55951971	CCCCCCATAGGAAGC[C/T]TCTCTCTGTCTGTCA	4067
rs749888930	snp	C/T			intron-variant, downstream-variant-500B	LYN	GRCh38.p7	8:55968348	GCAACCTCTGCCTCC[C/T]AGGTTCCAGTGATTC	4067
rs749909439	snp	A/G			intron-variant	LYN	GRCh38.p7	8:56008682	ACATTTGACCACATT[A/G]AAAACATTCTCTATT	4067
rs749909541	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55891701	CAAGTTTTATATTGT[A/G]TTTATTTTACCACAA	4067
rs749914739	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55890504	TAAAATGCTACAGCT[A/G]TGATGGAAAATCATA	4067
rs749951213	snp	C/T			utr-variant-3-prime	LYN	GRCh38.p7	8:56011345	TACCTAATATTTCTA[C/T]TTTTGATTTTATTTT	4067
rs749970445	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55901032	GGCATTTGCAGCAGT[A/G]CCTCTATGATGCCTG	4067
rs749992156	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55938891	CAGCTATGCTGTGCG[C/T]GAGTCTTTTAACCTT	4067
rs750007071	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55995724	TCCACACAGAGGCAG[A/G]GGGTGTAGAAGCACA	4067
rs750008694	snp	C/G	1.66524e-05	0.00288547	intron-variant	LYN	GRCh38.p7	8:55947771	TTTCCTCAGGCCACT[C/G]AGTCCTGCAGGCTGT	4067
rs750021201	in-del	-/AAATT			intron-variant	LYN	GRCh38.p7	8:56002609	TCCATCTCAAAAATT[-/AAATT]AAATTAAATTAAATT	4067
rs750055053	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55990519	AATATAAATTTCCCC[C/T]ATAAGAGATGGCTTT	4067
rs750055066	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55977512	CTTTTCATGCTCCTA[A/C]CATTTTGTTTTATTA	4067
rs750058822	in-del	-/AAG			intron-variant	LYN	GRCh38.p7	8:55897193	CTAATTTCTCCTGAT[-/AAG]GAGCTGAAAATCAAG	4067
rs750071425	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55967595	TGCTAGGATTACAGG[A/C]ATGAGCACCCAGCCT	4067
rs750102783	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55978399	GCTGAGGACCGCCAT[C/T]GCGGGCACGGGGTTG	4067
rs750109190	snp	C/T			intron-variant	LYN	GRCh38.p7	8:56008988	CATTATTTTCCAAAT[C/T]AATCCCTAAGTTTTT	4067
rs750118470	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55973720	ATTACTCTTTGGTGG[C/T]GGTATCTCTGAAGTG	4067
rs750161285	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55969204	CTTGAGCTTGGGAGG[C/G]TGATGCTGCAGTGAG	4067
rs750168305	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55899639	GTTATCATCCCTTTT[A/C]TTTTCTTTTCTTTTT	4067
rs750170132	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55993393	TATCTTCTCAGAGAA[A/G]AAGTACTCTCTCAAT	4067
rs750189728	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55912451	AAATTCTTGGCTGGG[A/C]ATGGTGGCTTATGCC	4067
rs750197405	snp	A/G	1.64817e-05	0.00287064	missense	LYN	GRCh38.p7	8:55947704	TTCAAGAAAGGAGAG[A/G]AGATGAAAGTCCTGG	4067
rs750203949	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55907358	TCAATAAAATAAGTC[A/G]AACAGATAAGAATAT	4067
rs750257239	in-del	-/T	6.7348e-05	0.00580254	intron-variant	LYN	GRCh38.p7	8:55946522	GCAACATAGTTAAAA[-/T]TTTTTTTCTTTACTA	4067
rs750282181	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55958074	GGAGCAGGAAGTCAG[C/G]AGCTAGGCAGCCTGG	4067
rs750324728	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55880739	TGCCGAGGAGCAGTC[C/T]GGTGCTTTTGCCGGC	4067
rs750338648	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55882096	GTTACCCACATTTAG[C/T]GTGGGTAACTAAATG	4067
rs750347203	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55984482	CTTGGAGCTGTCAGA[C/T]CCCAACACTCAAAGT	4067
rs750352479	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55996851	GAGAGTGAATCTTGC[C/T]GGGCGTGGTGGCTCA	4067
rs750361940	snp	A/T	3.29462e-05	0.00405857	missense	LYN	GRCh38.p7	8:55969744	ATTTCCTGAAGAGCG[A/T]TGAAGGTGGCAAAGT	4067
rs750366411	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55991711	CAGGCGTTTTCAGGA[A/G]ACAATCACCTTGCTC	4067
rs750432645	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55911026	CTCAGCCTACCAGGT[A/G]GCTGGGCCTACAGGC	4067
rs750473102	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55954181	CTTGCTCTTTCTTGC[A/G]ACTTAGTAATTCTCT	4067
rs750476951	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55979226	TTTTGTATTATTAGT[A/G]GAGTTGGGTTTCACC	4067
rs750502159	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55930974	AGTTCTTACTCCCAC[A/G]GACAATTAGAGTTTG	4067
rs750529225	in-del	-/A			intron-variant	LYN	GRCh38.p7	8:55997159	CAGTGAGACTGTCTC[-/A]AAAAAAAAAAAAAAA	4067
rs750556850	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55914826	CCTGTTCATTTTGTT[A/T]GTAACAATAGAGCCA	4067
rs750621485	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55920258	GGACTTGGGGACGCA[G/T]CAGACATTATCTGGA	4067
rs750625932	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55992889	TGAGGGAGGATCTCT[C/T]ATGACCCAATCACCT	4067
rs750658967	snp	C/G/T	3.30105e-05	0.00406256	intron-variant	LYN	GRCh38.p7	8:55999374	CATGACTTTTTTGTT[C/G/T]AAGTTTAAATACCCA	4067
rs750673482	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55976681	ATGGAGCGTAGTAGG[A/G]TGGGCTAGCAGGTGG	4067
rs750675561	snp	C/T	1.64787e-05	0.00287038	synonymous-codon	LYN	GRCh38.p7	8:55999524	CCTATACGAAATTGT[C/T]ACCTATGGGAAAATT	4067
rs750722940	snp	C/G	1.66482e-05	0.0028851	intron-variant	LYN	GRCh38.p7	8:55942020	CTCAGGGGAGAATTC[C/G]CACAGCAAGATCAAA	4067
rs750734444	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55949707	TGTGTTGTGAACATT[C/G]AAAACCCTCACTCCT	4067
rs750796234	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55910607	CTTTGCTCCTTCTGG[A/G]CAAGATTGCTTTGGT	4067
rs750821548	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55943175	AATCTACTTCATTTC[C/T]GAGCTTATATCCTTT	4067
rs750849759	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55988809	ATCACATTCAGCCCC[G/T]CAGTGAGGTTCCTTT	4067
rs750850213	snp	C/G			intron-variant	LYN	GRCh38.p7	8:56002051	TTTGGGAGGCTGAGG[C/G]AGGTGGATCACCTGA	4067
rs750884766	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55933831	ATTCTAGTAAATGCA[G/T]TGATTAAAACTGTGC	4067
rs750912511	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55887269	AAATCAGCCTGTGCA[A/G]TTTGTCTCAAACAAA	4067
rs750913605	snp	C/T	3.29506e-05	0.00405884	synonymous-codon	LYN	GRCh38.p7	8:55953911	ATGGGATAAAGATGC[C/T]TGGGAGATCCCCCGG	4067
rs750950688	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55971516	GTCACACTTGTACAG[C/G]GCTATGGAACATCGG	4067
rs750951328	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55895309	CAAGTGAAGAAGTGA[A/G]TCCCTTAGTTGGAAA	4067
rs750953537	snp	A/G	5.66535e-05	0.00532199	intron-variant	LYN	GRCh38.p7	8:55966664	TGAGCCACCTCCCCC[A/G]GCTAGATTTTCTGTT	4067
rs750989927	snp	C/T	1.65537e-05	0.0028769	synonymous-codon, intron-variant	LYN	GRCh38.p7	8:55941893	AAAGGGAAAGACAGC[C/T]TGAGTGACGATGGAG	4067
rs751028436	snp	A/T	3.67363e-05	0.00428565	intron-variant	LYN	GRCh38.p7	8:55966682	TAGATTTTCTGTTTT[A/T]TAAAGCATGCCCGCC	4067
rs751043170	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55898679	TATGTTCACAGAGTT[G/T]TGCAATCATCACCAC	4067
rs751043602	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55944222	ATAGGAATATTAATA[A/G]ATTTAATTGTGTGAT	4067
rs751056729	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55926603	TCTAATGAAATTCTA[C/T]TGTATTTTAAACCAT	4067
rs751113956	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55937966	CCTCCCAAAGTTCTG[A/G]GATTACACTTGTGAG	4067
rs751125035	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55949822	GTACAATTCAGTGAT[A/T]TTTTTAGTATAGTCA	4067
rs751126842	snp	A/G			intron-variant	LYN	GRCh38.p7	8:56007747	TAAAGCAAACGTTTC[A/G]TAAAACCATATTGAC	4067
rs751187545	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55910691	CTAAGATATATTCAG[A/G]TTTCACTTTTGTTCT	4067
rs751194817	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55975599	ATGCAGTACTTACAT[A/G]TTGGGCACTTAAATG	4067
rs751232245	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55988545	AATTCTTCTTTTTCT[C/T]AAGCATAGGAAGACA	4067
rs751243342	in-del	-/TA			intron-variant	LYN	GRCh38.p7	8:55942333	GTATATATATGTGTA[-/TA]TATATATATGTGTAT	4067
rs751280578	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55905279	TAGCCAGGCGTGGTG[G/T]CAGGCACCTGTGATT	4067
rs751314014	snp	G/T	1.64781e-05	0.00287033	splice-donor-variant	LYN	GRCh38.p7	8:55950559	TTAGAAACAGAAGAG[G/T]GAGTCCTCATGTGTT	4067
rs751318803	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55990039	AGGTCAGGAGTTTGA[C/G]ACCAGCCTGGCCAAC	4067
rs751322028	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55909429	TCTGACTTGGACATG[G/T]TCAGTCATAATCCCA	4067
rs751335391	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55916472	TACTGCTCTGGAAGG[G/T]TGCGTGCGAATATGG	4067
rs751363358	snp	A/T			upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55877977	AAGGAGTTTACCAGT[A/T]GTTGAGGAGACAAGC	4067
rs751395536	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55946184	CAAAGAAGAGGAGGA[A/G]CTAGGATGAGGTGAG	4067
rs751409304	snp	C/T			intron-variant	LYN	GRCh38.p7	8:56008593	AAAATGTTATTATTA[C/T]AATGATCTTTTTTAC	4067
rs751432539	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55927910	GTACATACGTTTTCA[A/T]CTCACTTGGGTAAAA	4067
rs751449475	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55915481	AAGCCAAGGCAGGCG[A/G]ATCACCTGAGGTCAG	4067
rs751472652	in-del	-/AGTGAGACTAAGACTT			intron-variant	LYN	GRCh38.p7	8:55929303	AGATTAGTGAGACTA[-/AGTGAGACTAAGACTT]AGTGAGACTAAGAAT	4067
rs751487927	snp	A/G	1.67646e-05	0.00289517	intron-variant	LYN	GRCh38.p7	8:55998316	TCACCTACCCTACAT[A/G]TGAAAATGGGAGCCT	4067
rs751490724	snp	A/G			intron-variant, downstream-variant-500B	LYN	GRCh38.p7	8:55968282	TTTTTTTGAGACAGA[A/G]TCTCACTCTATCACC	4067
rs751508330	snp	A/G	1.69043e-05	0.00290721	intron-variant	LYN	GRCh38.p7	8:55950414	TGATACATGCATGGA[A/G]TATGTAATCTTTTAG	4067
rs751521252	snp	A/C	1.64925e-05	0.00287158	synonymous-codon	LYN	GRCh38.p7	8:55998492	TAATGAGTACACAGC[A/C]AGGGAAGGTATGTTG	4067
rs751570949	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55913988	GCTAAGCTCTATCAG[A/T]TGAGCAATGAGCAGT	4067
rs751589745	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55941338	TAGTGTTGTAGATAG[A/C]GCTCATTTTCTGAAG	4067
rs751618370	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55952278	TTAATCTATAGTTAG[G/T]CCAGGCACAGTGGCT	4067
rs751622161	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55925405	TGGGATTACAGGTCC[A/G]AGCCACTGCGCTCCA	4067
rs751637724	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55955248	AGTGACTTTTAAACA[C/T]GGCACATACTGAGCC	4067
rs751641349	snp	A/G			intron-variant	LYN	GRCh38.p7	8:56001269	GAATGAATGAATGAC[A/G]CACCTAGGCCATTTG	4067
rs751652988	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55992708	TAGTGCTCTGCTTCT[C/T]AAACTCTAAGCTCTG	4067
rs751691448	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55912657	TCTTGAACCTGGGAG[A/G]CAGAGGTTGCAGTGA	4067
rs751712614	in-del	-/T			intron-variant	LYN	GRCh38.p7	8:55937404	TTCTTGATTGTTTGA[-/T]TAAGAATGTCCAAAT	4067
rs751731014	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55976435	CCTTTGTCTCCAGCA[C/G]TTGGCTTGCTCTCCC	4067
rs751747052	snp	A/G			intron-variant	LYN	GRCh38.p7	8:56006005	TGGGAGGATCACCGA[A/G]CCCAGGGAGTTTGAG	4067
rs751766151	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55963808	TGCAAGTTCCTTGCA[G/T]TTATATGTATCATAT	4067
rs751785632	in-del	-/ACTT			intron-variant	LYN	GRCh38.p7	8:55917678	CCCTGCCTTTTAGGC[-/ACTT]ACTCTTCCAGTGTCT	4067
rs751789349	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55974464	TCTAGGAAGTTCTCG[A/T]CCTTTTTGAGTAGGA	4067
rs751797343	snp	C/T	5.06795e-05	0.00503361	intron-variant	LYN	GRCh38.p7	8:56009892	TTTCTGTTCTTTTTG[C/T]TTTTTTCCACCCTAG	4067
rs751804664	snp	C/T	1.65337e-05	0.00287517	missense	LYN	GRCh38.p7	8:55950746	CACCAGGAAATAGCG[C/T]TGGAGCTTTCCTTAT	4067
rs751816885	in-del	-/T			intron-variant	LYN	GRCh38.p7	8:55896662	AGTATAATAAAAAAA[-/T]TTTAAAAAAAAGAAA	4067
rs751817428	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55964732	GAGAAGAGAAGAGAA[A/G]AGAAAAGAGTACATA	4067
rs751817767	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55991896	AAAATGTGCATTGGC[C/T]ATGCTATTTGAATCA	4067
rs751839684	snp	C/G	3.29908e-05	0.00406132	intron-variant	LYN	GRCh38.p7	8:55951956	TTTACTTACACTTTT[C/G]CCCCCATAGGAAGCT	4067
rs751842537	in-del	-/T	1.65026e-05	0.00287246	intron-variant	LYN	GRCh38.p7	8:55950672	GGAAATGTTGAAATG[-/T]CTTCACAGGTGGTTT	4067
rs751861132	in-del	-/C			intron-variant	LYN	GRCh38.p7	8:55896896	AGGTGCCCGCCATCA[-/C]CCCCAGCTAATTTTT	4067
rs751870938	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55897478	AGAGTCTAGTAACAG[A/T]TCTGTCTTACTGTTC	4067
rs751885110	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55895088	CTCCCAAAGTGCTGG[C/G]ATTACAGACGTGAAC	4067
rs751914501	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55971421	GGGCCATACTTACAC[A/G]GATCAATGAGGCCCT	4067
rs751951389	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55920829	CTGCCTCAGCCTCAG[C/T]GGGATTATAGGCATG	4067
rs751954482	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55938262	CATATTGTAAAACTT[C/T]TGCAATGAACAGACT	4067
rs751958379	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55985160	TAGAAAGCTGCACTG[C/T]TGGGGAGGAACTGTA	4067
rs751982860	snp	A/G			intron-variant	LYN	GRCh38.p7	8:56000285	TAACCACCTTTGTTT[A/G]TCAGTGGGAGGCCCT	4067
rs752007163	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55985567	GCGCTGTCTTTATAC[A/G]GGAATTCTTTTCAGA	4067
rs752011239	snp	A/G			utr-variant-3-prime, downstream-variant-500B	LYN	GRCh38.p7	8:56011906	CAAGTATTACCCAAT[A/G]TGTTACATGGAGAGG	4067
rs752019975	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55959873	TGCTGTTTTATGGAT[G/T]ACTTATAATAACACT	4067
rs752059437	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55958131	CACCCCCTGTTCTGT[C/T]GTAAGGTGTAAGTCT	4067
rs752068625	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55884899	TTCTCTCATTACTGA[A/C]TTAGCTGGCAGCATT	4067
rs752088089	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55981373	GTGCCTTGTATATAG[C/T]AGATGCTCAAAAATG	4067
rs752141410	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55970656	TTAGGAAATTGCTAC[A/G]GCCTTCTTGGGAATA	4067
rs752141606	in-del	-/TA			intron-variant	LYN	GRCh38.p7	8:55942266	GTGCAAAGACCCCAC[-/TA]TATATATATACACAC	4067
rs752153494	snp	C/G			upstream-variant-2KB	LYN	GRCh38.p7	8:55877088	TGTTTCTGTTTAATG[C/G]ACACCTTATTTAATA	4067
rs752200104	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55949693	ATTTATTCTTTCTTT[A/G]TGTTGTGAACATTCA	4067
rs752213018	snp	A/G	1.69387e-05	0.00291016	intron-variant	LYN	GRCh38.p7	8:55946537	TTTTTTTTCTTTACT[A/G]TTAGAGCTTCTATAA	4067
rs752227699	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55919399	ATATGAATGCTCTGT[C/T]AATATAGTGCTTTTC	4067
rs752244751	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55936878	GGTTGTACCTGAGAC[C/G]TTTGATTACCTAGCA	4067
rs752251461	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55949095	TGCCTTTCTGCTGAG[G/T]ACTCGAGCATGGTGC	4067
rs752277258	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55920666	AAGTCCTTTGCTGCT[G/T]TACTTCAGGAAATTT	4067
rs752286513	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55966397	AATTGAGACGGAGTC[A/G]CACTCTGTCACCCAG	4067
rs752320083	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55987230	CCACACTGGGGAACA[A/T]GATGAAACACCGTCT	4067
rs752325671	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55974729	AAGAGATGTGTTAGA[C/T]GCTCATATTCCACCT	4067
rs752362811	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55887444	GTGACAGTTGAGTGC[C/T]GTTTTTACTTCTGTA	4067
rs752411201	snp	C/G/T	3.29719e-05	0.00406018	synonymous-codon	LYN	GRCh38.p7	8:55966845	CGTGAGGCTCTACGC[C/G/T]GTGGTCACCAGGGAG	4067
rs752468894	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55926563	AACCTAAAATTGAAG[A/G]AGTTTGGGAATTAAG	4067
rs752520304	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55937716	TTTTGTTTTTTTGAT[A/G]GAGTCTTGCTCTGTC	4067
rs752581266	snp	G/T			intron-variant	LYN	GRCh38.p7	8:56007610	ATGTCTTCTTTCAGC[G/T]GTTTAAATTCAGGAA	4067
rs752602062	in-del	-/GTG			intron-variant	LYN	GRCh38.p7	8:55892281	CAAAAATAGCCAGGT[-/GTG]GTGGCACACACCTGT	4067
rs752636074	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55896800	TTGGAGTGCAGTGGC[A/G]TGATCTCGGCTCCCC	4067
rs752641024	snp	C/T			intron-variant	LYN	GRCh38.p7	8:56006426	AGGGCCCTGTGTGAC[C/T]GAAGACTGTCATAGT	4067
rs752714014	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55966175	GTGCCAATAAAAACG[A/T]TTTTTTGCTACTATT	4067
rs752726842	in-del	-/CTTTT			intron-variant	LYN	GRCh38.p7	8:55899634	GTACAGTTATCATCC[-/CTTTT]CTTTTCTTTTCTTTT	4067
rs752739111	snp	A/G	3.30191e-05	0.00406306	missense	LYN	GRCh38.p7	8:55950712	ATAACCAGGAAGGAC[A/G]CAGAAAGGCAGCTTT	4067
rs752766518	in-del	-/TGG	1.64746e-05	0.00287002	cds-indel	LYN	GRCh38.p7	8:55947664	CTTGTACCCCTATGA[-/TGG]CATCCACCCGGACGA	4067
rs752787468	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55885953	TTTGCCCTTAAGTGA[A/G]GGGTGGGGCGGGGTG	4067
rs752809156	snp	A/G			intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55923558	ACAACTTTTTTTTTT[A/G]AGACAGGGTCTTGCT	4067
rs752883406	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55991035	ATGTGAATATACCAA[C/T]AAATAGAGACACGCC	4067
rs752897016	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55972499	GAAATCCCATACCTT[A/C]CACTTCTAGTTTCTG	4067
rs752897167	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55984233	GAGGTTCCGGGTGGT[C/T]GTGAGTTTTGGGGGG	4067
rs752931705	snp	A/C	1.6599e-05	0.00288084	missense	LYN	GRCh38.p7	8:55952105	CAGCGACATGATTAA[A/C]CATTACCAAAGTAAG	4067
rs752953587	snp	C/T	1.64928e-05	0.00287161	intron-variant	LYN	GRCh38.p7	8:55951961	TTACACTTTTCCCCC[C/T]ATAGGAAGCTTCTCT	4067
rs752973616	snp	C/G			intron-variant	LYN	GRCh38.p7	8:56002550	GAGGTTGCAGTGAGC[C/G]AAGATTGCACCACTG	4067
rs752996643	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55962758	TGCTAAAGGAATACC[C/T]GAGACTGGGTAACTT	4067
rs753021909	snp	A/G	1.64773e-05	0.00287026	synonymous-codon	LYN	GRCh38.p7	8:56010020	GTGCTGGAAAGAAAA[A/G]GCAGAAGAGAGACCA	4067
rs753041622	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55969626	TCATTTTGTGGGGAG[G/T]TCCCCTGTAATAGTA	4067
rs753056410	snp	C/T			utr-variant-3-prime	LYN	GRCh38.p7	8:56010767	TGCACATCTCTCTCT[C/T]TTCCAGCAGGAGGAG	4067
rs753062258	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55892755	AACAGGATTCGAGGG[A/C]ATTTTTTAAAAAGTT	4067
rs753102245	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55930367	ACAACTCTTAAAGTG[G/T]GACATAAATACACTA	4067
rs753149764	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55952834	GGTAAAGTCAAACGG[A/G]TATAACACTACCACT	4067
rs753153413	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55941253	AACCACTCAGCTTCA[C/T]ATCCAGCATGTGCCT	4067
rs753155414	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55929480	CTTTACATTTTATAA[A/C]AGGATATTAAACTTA	4067
rs753228767	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55991790	CTGTGCTCAGTAAAC[C/T]GCTTTTTAAAAACGA	4067
rs753270687	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55980021	AGGGCTCAGAGCCCA[G/T]GTGCACAGGCAGCAT	4067
rs753317123	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55917835	AGGCTGGAATAGATT[C/T]TCCCAAATCTCCTGA	4067
rs753326823	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55906347	TTTTGTTTTGTTTTG[C/T]TTTGTTTTGTTTTGT	4067
rs753344315	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55986072	TACTCAGGAGGCTGA[A/G]GTAGGAGGATTGCTT	4067
rs753348752	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55880822	TTGGGGGAAGGGCGT[A/G]AGAGTCAGTTCCCAC	4067
rs753370248	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55929244	GAGAAGCAGGGATCC[A/G]TAGAATAGATCCTTC	4067
rs753393373	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55905976	CAGAAACCACCAAGT[A/G]CAGCATAGTTCTACA	4067
rs753400659	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55958378	ATTGTTTTATACAAA[G/T]TTTTACTTTTTATTT	4067
rs753429979	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55961086	TTTGCTTGATAAATT[C/T]TCATTTGAGCCAACT	4067
rs753463669	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55998276	ATTCATAAGTTTTCC[A/G]GTTTTCCTTGATGGC	4067
rs753470185	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55968623	TGCTTTCCATGGGTG[A/G]TCTCACTTAGTCTTT	4067
rs753515425	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55964844	CTGTTGTTTTACTCA[A/G]CAGGCTTCCAGTCAT	4067
rs753547364	snp	C/G			utr-variant-3-prime	LYN	GRCh38.p7	8:56011623	AGGCTTAACAGGCAT[C/G]ATTAAAATTTCATTC	4067
rs753592677	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55928112	TTTCCTGTTTAATAG[A/G]TATATAGTAGTAGAG	4067
rs753605132	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55975408	TGGGAGGCACAGGTT[G/T]GGTTTCCCACAGCCT	4067
rs753612014	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55936678	AGTGCAGCTTTTAGA[C/T]AGAAGGAATAGATTC	4067
rs753621314	snp	A/G	1.65116e-05	0.00287324	missense	LYN	GRCh38.p7	8:55966867	ACCAGGGAGGAGCCC[A/G]TTTACATCATCACCG	4067
rs753649452	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55897610	ATATAAGCACTCTTA[A/G]CCATCAGAATAACTT	4067
rs753668381	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55949072	TGCCTCCTCCCTGGC[C/T]CCATGCCTGCCTTTC	4067
rs753747947	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55974675	TTTGCCAATATCATC[C/G]AAAGTGGGTCTCTTC	4067
rs753817874	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55896112	GCAATTAAAAAAAAA[A/G]AACAAGTTTTAGCTA	4067
rs753821913	snp	A/G	1.65083e-05	0.00287296	intron-variant	LYN	GRCh38.p7	8:55998513	AGGTATGTTGCACTA[A/G]TGATCTTTAGATGTT	4067
rs753832304	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55911229	TGTATATATATATAC[A/G]TATACATATATATAT	4067
rs753843496	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55907516	TACATCTACCAGAAC[C/T]GATGTCAGCACAGTT	4067
rs753865571	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55882116	GTAACTAAATGAGAG[G/T]CTCCACTCAGCACCG	4067
rs753903784	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55945924	CACGAAATCACCAGG[G/T]TCCCACCTCTTCCGT	4067
rs753922290	snp	C/T			intron-variant	LYN	GRCh38.p7	8:56001377	CATGTAAGAGCAGCC[C/T]CTCTTACTCTGCTGA	4067
rs753954053	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55997475	CTGGTTCATAGATGG[C/G]ACCATATAGCTGTGT	4067
rs753978273	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55905138	TGACCTGGCTGGGTG[G/T]GGTGGCTCGTGCCTG	4067
rs753989883	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55982356	GCATTATACTTACTG[A/G]TTAACCATTTCAAAA	4067
rs754010386	snp	G/T			utr-variant-5-prime, missense	LYN	GRCh38.p7	8:55879855	CTCTCCCGCCGCGCC[G/T]GGCCGCGCTGCCGCT	4067
rs754011006	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55943432	AGTACAAAAATTAGC[C/T]GGGTGTGGTGGTGCG	4067
rs754030537	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55982161	TTTTCCACCCAGCGC[C/T]CCCAGTGTCTGTAAC	4067
rs754067250	in-del	-/CTAA			intron-variant	LYN	GRCh38.p7	8:55951211	TCACGCCACTGCACT[-/CTAA]CTAGCCTGAGTGACA	4067
rs754069760	snp	C/T	1.66604e-05	0.00288616	intron-variant	LYN	GRCh38.p7	8:55941847	TCATTACTTTTATGT[C/T]TCAACAGGAAATATG	4067
rs754081816	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55983117	GCCTAGCAGCTTTCT[A/G]CATTTCCAGTTCAAG	4067
rs754094485	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55956305	TGTTATTATTGCCGT[C/T]GACCACCTGAGATTA	4067
rs754127012	snp	A/T			upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55877902	ATTTTAAAGCACCCA[A/T]CATAATTTCTGGGAG	4067
rs754163396	snp	A/C/G	0.000583661	0.017074	synonymous-codon	LYN	GRCh38.p7	8:55953881	GGCTTGTATTAGTCC[A/C/G]AAGCCACAGAAGCCA	4067
rs754183271	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55916364	ATGGCCCTGTTTTCT[A/G]ACTTAAAAATGGTGC	4067
rs754270013	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55978566	AGACAGTCATATAAA[C/T]AGGGGTTGGATGAGG	4067
rs754276890	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55943682	CAAACCTTTCTGCCT[A/G]CCCTCCCCTCAATAT	4067
rs754289412	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55962610	GCATTCATGCTTTTG[A/G]GTGTGGCTATGGTTT	4067
rs754329278	snp	A/G	1.64789e-05	0.0028704	missense	LYN	GRCh38.p7	8:56010046	GACCAACGTTTGACT[A/G]CTTACAGAGCGTCCT	4067
rs754350555	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55884931	CTTATTTGCCACAGA[A/G]CTATTTCTTAAAAGC	4067
rs754357226	snp	A/G			intron-variant	LYN	GRCh38.p7	8:56002361	GAGGCGGAGCTTGCA[A/G]TGAGCTGAGATCGCG	4067
rs754362086	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55885862	GTCATTTGCCTGCAG[C/T]CCCACCTTCCTTACC	4067
rs754425998	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55961233	GAGTGCTCTCAAGGT[A/G]CCACATCAGCTTTCT	4067
rs754484935	snp	A/G	1.65425e-05	0.00287593	missense, intron-variant	LYN	GRCh38.p7	8:55941908	TTGAGTGACGATGGA[A/G]TAGATTTGAAGACTC	4067
rs754500406	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55885208	ACATCCTATAGAACT[G/T]CATGAATCGGGATAC	4067
rs754508092	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55919137	AAGCAGAAATAATAG[A/G]GGAGAAAGAGGATCT	4067
rs754544360	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55906378	TTTTGACAGAGTTTC[A/T]ATCTGTCGCCCAGAC	4067
rs754565526	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55880842	TCAGTTCCCACTTTC[C/G]TGCATTCTCTGGGCC	4067
rs754566483	in-del	-/AAATT			intron-variant	LYN	GRCh38.p7	8:56002605	GAGACTCCATCTCAA[-/AAATT]AAATTAAATTAAATT	4067
rs754567900	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55985563	CCAGGCGCTGTCTTT[A/T]TACAGGAATTCTTTT	4067
rs754670873	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55957590	GACAAGTAAAGTGAA[C/G]AAAGTAATTCAAATC	4067
rs754716227	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55888660	CTTGTAATCGTCATC[C/T]GCAAGTAGGTACTTG	4067
rs754746582	snp	C/G			intron-variant	LYN	GRCh38.p7	8:56006267	AAGAAATTTGTCCTG[C/G]TGCAAACAAACACTC	4067
rs754750038	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55954153	TGGCCTGCAAAATCT[A/G]TTTACTTCAGCTCTT	4067
rs754777611	in-del	-/T			intron-variant	LYN	GRCh38.p7	8:55916165	AATCTTCAGAAAAAA[-/T]TTTTTATTGAGATGA	4067
rs754788891	snp	G/T			upstream-variant-2KB	LYN	GRCh38.p7	8:55876546	TCCCCATCCCCCAAA[G/T]ACTTTGATTTAACTG	4067
rs754795794	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55992898	ATCTCTCATGACCCA[A/G]TCACCTCCTAAAGGC	4067
rs754799839	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55911674	CCTGGGGGCAGTCCT[A/G]TGAGCTGCGGGGCAC	4067
rs754803024	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55964968	TATCCAGCTTTTGCG[C/T]ACCAGGCAGCAGGAA	4067
rs754818990	snp	C/T			intron-variant	LYN	GRCh38.p7	8:56009317	ACAAATTTTGGCAAA[C/T]TGAATGCTGTCTTGA	4067
rs754884620	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55925746	CAGGTTCCTGAGGAC[A/G]CCCTGGACGCTGGTG	4067
rs754902575	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55935995	TGAAGACTTTGTTTC[C/T]CTAATCTGAGTCTCC	4067
rs754910196	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55907530	CTGATGTCAGCACAG[C/T]TAGGATCTTTACCTT	4067
rs754921780	in-del	-/ATAT			intron-variant	LYN	GRCh38.p7	8:55911192	TATATATATATACAC[-/ATAT]ACACACATATATATA	4067
rs754927668	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55971427	TACTTACACGGATCA[A/G]TGAGGCCCTCTACTC	4067
rs754931377	snp	C/T	1.64792e-05	0.00287042	intron-variant	LYN	GRCh38.p7	8:55950569	AAGAGTGAGTCCTCA[C/T]GTGTTGTCATCTTGG	4067
rs754931585	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55947787	AGTCCTGCAGGCTGT[C/G]CCCTTGTCTTGCTTC	4067
rs754940739	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55924829	TTTGGCTTCAAGCTT[A/C]GTCCAAAGAATGGTT	4067
rs754972605	snp	A/C			intron-variant	LYN	GRCh38.p7	8:56005158	CTATTCCCAGCCACA[A/C]AATTCTCTCCCCATA	4067
rs755011659	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55961616	GATGACTTCCCCCCT[A/G]ACCTTGGAAAGCGTT	4067
rs755038123	in-del	-/ACTC			intron-variant	LYN	GRCh38.p7	8:55987772	TGCTTAAGAGCACAG[-/ACTC]TTAAGCCTGGACCAG	4067
rs755055761	in-del	-/CTGTT			intron-variant	LYN	GRCh38.p7	8:55976155	GTCACAGTTGAAAAG[-/CTGTT]TGGAGATGAAAGCAG	4067
rs755061407	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55911558	GGCAGCAGGTGGAAA[C/T]GTACATTCACTACTT	4067
rs755068188	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55884941	ACAGAGCTATTTCTT[A/G]AAAGCTGTACTTACA	4067
rs755082235	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55972393	CTGCTTCTTGTACCT[A/G]TGGCTTTTCTTATTA	4067
rs755085942	snp	A/G			intron-variant	LYN	GRCh38.p7	8:56001393	CTCTTACTCTGCTGA[A/G]ATGCAAACCAGGGAA	4067
rs755087197	snp	A/C	1.64944e-05	0.00287175	intron-variant	LYN	GRCh38.p7	8:55951957	TTACTTACACTTTTC[A/C]CCCCATAGGAAGCTT	4067
rs755113566	snp	A/G			intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55922352	GCCTCAGCCTCCCCA[A/G]GTGCTGGGATTATAG	4067
rs755185456	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55944862	CAAACCCACACACCG[A/C]TTTTTCCTCTTGTTC	4067
rs755200531	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55905272	AAAAAATTAGCCAGG[C/T]GTGGTGGCAGGCACC	4067
rs755202192	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55895405	GTATGGATTAGTAAC[A/G]CTGTAGTAGCTAATG	4067
rs755226563	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55928306	AAGCGCCACCACGCC[C/G]GGCTAGTTTTTGTAT	4067
rs755251528	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55904354	TATGAAATATGATAT[G/T]AAATTCAACTTTACT	4067
rs755273291	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55979824	TGACACCCTGCCCAA[A/G]GCTCAGAGGGATGCC	4067
rs755344860	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55901224	AATAGTTCTCCGATT[A/G]GAATAGCAGTTACAA	4067
rs755367546	snp	C/T	1.67699e-05	0.00289563	intron-variant	LYN	GRCh38.p7	8:56009899	TCTTTTTGTTTTTTT[C/T]CACCCTAGGGAGAAC	4067
rs755385445	snp	A/G			utr-variant-5-prime, missense	LYN	GRCh38.p7	8:55879886	CGCTCCCCGGCCGTG[A/G]CGCCTCCGGGCCAGA	4067
rs755388433	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55891903	ACTCTTCGTCATTTA[A/G]TACATGGCCACGTGG	4067
rs755396094	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55911944	GGGCGTCCAAATGGA[A/G]ATGTGGAAGTTTGAT	4067
rs755416038	snp	C/T			intron-variant	LYN	GRCh38.p7	8:56002417	GAGCGAGACTCCATC[C/T]TAAAAAAATAAAAAA	4067
rs755493560	snp	C/T			intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55923460	GCTTGCTTCACAGCA[C/T]TCTGAGTGTCTATAA	4067
rs755525236	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55957419	ACGTGTCTGTCATGA[A/C]AAGAAATGTAGAGGG	4067
rs755528329	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55952515	CAGTGAGCTGAGATC[A/G]CGCCACTGCACTCCA	4067
rs755528340	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55939113	ACATTTCTGGTACTT[C/T]CATACAGCATAAGGA	4067
rs755529354	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55926077	CTTAAGAAATCTTTA[C/T]CACTTTCAAGGTGAT	4067
rs755533350	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55964323	CCTGCCTCTCAAAGT[A/G]CTGGGATTACAGGCA	4067
rs755566196	snp	A/G			upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55879257	GATAGGCATCCTCAC[A/G]TCCATTGTCCTGGGA	4067
rs755568229	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55983209	CTGCTAGAAACAATG[C/T]CCCACCTTCCCTTTC	4067
rs755581287	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55951014	TTGGGAGGCTGAGGC[A/G]AGAGGATCACTTGAG	4067
rs755607069	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55983535	CCCCCAGTTCTTCCC[C/T]ACCCGCCCTCTCTTG	4067
rs755615369	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55883254	AAATCATTAAGTTGC[A/C]GACCATCTGTGCTTA	4067
rs755660385	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55995777	GGTGGAGGGCTGAGC[C/T]GGGGCCGGGTCATAC	4067
rs755687135	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55916594	CGATGATCCCTGAGT[G/T]CCAGATGTGAAGGAA	4067
rs755707578	in-del	-/G			intron-variant	LYN	GRCh38.p7	8:55917585	TAATGAACTGTGACA[-/G]GGGCTAGCAAGAAAG	4067
rs755713431	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55996973	TAAAAATACAAAAAC[C/T]AGCATGGTGAAACCC	4067
rs755720048	in-del	-/TGTGTG			intron-variant	LYN	GRCh38.p7	8:55908987	GTATTCCATTGTGTA[-/TGTGTG]TGTATATATATATAT	4067
rs755723528	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55903887	CAGGCATGGTGGCAT[G/T]GCCCTGTAGTCCCAG	4067
rs755732978	snp	A/G			intron-variant	LYN	GRCh38.p7	8:56006643	TGCCATTTGAGGATG[A/G]TGCTCTGTCTTAACT	4067
rs755751814	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55927111	CATTAATTAAAATCT[A/G]CAGTTTTCATTAGGA	4067
rs755780616	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55890543	CCTCAAAAAATTAGA[C/T]ATAGAATTGCCATAT	4067
rs755781051	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55901119	GCACTTGGGCACTTC[A/G]TGGCCGTGTGTCTCA	4067
rs755818730	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55938993	CAATATATTATAAAT[A/G]TGTAATAGAAGAATA	4067
rs755823224	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55892577	AGGCAGGGTCTTGCT[C/T]TGTCACCCAAGATGG	4067
rs755831693	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55924304	GGAATCATGGTACAG[A/G]CCTGTTCTATACCAT	4067
rs755861798	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55897538	TCCATTTTAACAGAA[A/C]ACCTACTACTACTAC	4067
rs755880372	snp	C/T			intron-variant	LYN	GRCh38.p7	8:56004925	GAGTAGCTAGGACTA[C/T]AGGCGCATGCCACCA	4067
rs755911025	snp	A/T			intron-variant	LYN	GRCh38.p7	8:56002918	GAAGACTTGATTCAT[A/T]GCACAGAAATCGGTA	4067
rs755933707	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55886209	TAAATTCCTTGTTAA[A/G]TTCTTGGGATAGAAC	4067
rs755966667	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55896362	AATAGCAGGGACATG[A/G]ATGCAGCTGGAAACC	4067
rs755979678	in-del	-/AC			intron-variant	LYN	GRCh38.p7	8:55911182	TACACGTATATATAT[-/AC]ATATATACACACACA	4067
rs755986648	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55896851	TCAAGCAATTCTCCC[C/T]ACCTCAGCCTCCTGA	4067
rs756005159	snp	A/G/T			intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55923831	GGCGTGAGCCACCGC[A/G/T]CCCGGCCAAGATCAA	4067
rs756017441	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55984493	CAGATCCCAACACTC[A/G]AAGTCATTCTTGACC	4067
rs756061655	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55905532	GATGTCCTGGAGTGC[C/T]GAGATGTGTCCAGAA	4067
rs756141161	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55970740	GCTGGACACAGGTTC[C/T]GTAATAGAGCATCGT	4067
rs756154482	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55946316	TTTTTCCCTCTGTGC[C/T]CCTGTTCTTTCTGAC	4067
rs756198374	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55894594	CTGGAGTTCATTGGC[A/G]CTATCTTGGCTCACT	4067
rs756216204	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55895326	CCCTTAGTTGGAAAT[A/T]AAGTAGGAAGAGATG	4067
rs756222798	snp	A/G			upstream-variant-2KB	LYN	GRCh38.p7	8:55877239	CAAGCTCTACGCTTC[A/G]GGCCATTTATTTTTA	4067
rs756231240	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55981439	GATTGACTATATTCC[A/G]TTTAAAACAATAAAT	4067
rs756232138	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55930992	CAATTAGAGTTTGAA[G/T]GACCTTAGGCCATGG	4067
rs756238523	snp	A/G			intron-variant	LYN	GRCh38.p7	8:56000511	AGGTGGGTGAATCAC[A/G]AGGTCAGGAGTTCGA	4067
rs756279910	snp	C/T			upstream-variant-2KB	LYN	GRCh38.p7	8:55877018	AGGTTCCTGTGAGTC[C/T]CTGGACACAACATTT	4067
rs756285817	snp	A/C	1.67377e-05	0.00289284	intron-variant	LYN	GRCh38.p7	8:55998320	CTACCCTACATATGA[A/C]AATGGGAGCCTATTT	4067
rs756307712	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55960067	TTTCTTTTTGGAGTC[A/G]TGACAACATTCTAAA	4067
rs756327261	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55955340	AGGTAAACTGTAATT[A/G]CATGACTTCACATTC	4067
rs756373969	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55938165	ATAGAAAGAGAAATC[C/T]CCAGCCTCACATTTT	4067
rs756424998	in-del	-/C			intron-variant	LYN	GRCh38.p7	8:56002106	GCCAACATGGCAAAA[-/C]CCCATCTCTACTAAA	4067
rs756456343	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55988892	AGTGAAAAAAAAAAA[C/T]CCAAAAAACAAAAAA	4067
rs756477645	snp	C/T	1.64914e-05	0.00287149	intron-variant	LYN	GRCh38.p7	8:55951963	ACACTTTTCCCCCCA[C/T]AGGAAGCTTCTCTCT	4067
rs756485340	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55950942	CCTCAGTGATTAGTT[A/G]TGCTACTAAAAGTAA	4067
rs756488014	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55974697	GGTCTCTTCTTCTGT[C/G]TCTTTGTCTGGAACG	4067
rs756507286	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55977655	CAGTGGCTCATGCCT[A/G]TAATCCCAGCTCTTT	4067
rs756509050	snp	A/T			intron-variant	LYN	GRCh38.p7	8:56001300	ATCTCTAGACAGTCG[A/T]TGGATGAGAAAGAAG	4067
rs756527068	in-del	-/G			intron-variant	LYN	GRCh38.p7	8:55948439	TGAGCTACAGCAGCT[-/G]TGTTGGGAAATTCTC	4067
rs756543881	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55922043	GCTGTAGGGAAGCAT[A/G]AGGAAAGGAGTGGGT	4067
rs756544051	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55987566	GGATTATGGGTGCCC[A/G]CCACCACACCTAGCT	4067
rs756556547	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55883687	GAGAGCATCATTTAA[C/G]TGAAAATATAAATTA	4067
rs756614709	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55909661	TCCAGTTTTCATTAT[G/T]TGAGAAATCTCCATA	4067
rs756617689	in-del	-/TAAC			intron-variant	LYN	GRCh38.p7	8:55916145	TGATAGTTTCATGTT[-/TAAC]TAAATCTTCAGAAAA	4067
rs756632109	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55933902	CCCTGGGTCTACCTA[C/T]GGCTGTGCTTATGTC	4067
rs756657961	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55941103	CTTCCTAGGCCCCTA[C/T]CTATGTTTAGCTGGA	4067
rs756721138	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55890408	CATGTTAAAAAAGAA[C/T]ACAACAACAAAAATC	4067
rs756737758	snp	C/T	4.95315e-05	0.00497627	synonymous-codon	LYN	GRCh38.p7	8:56009933	TGCCGACGTGATGAC[C/T]GCCCTGTCCCAGGGC	4067
rs756743115	in-del	-/CA			intron-variant	LYN	GRCh38.p7	8:55942784	AACAAGACTCTGTCT[-/CA]AAAAAAAAAAAAAAA	4067
rs756743350	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55994495	ATGCGGGATGTGGGT[A/G]GGTGTGACAAATGCC	4067
rs756764174	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55967552	AACTCCTGAGCTCAG[A/G]CAATCTGCCTGCCTC	4067
rs756794010	snp	C/T			intron-variant	LYN	GRCh38.p7	8:56007784	TATGTGCAGTGCTTT[C/T]TGACCTTTTCTGTTT	4067
rs756827844	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55926642	AGACACAGCAGGTAA[C/T]GGCCTGCCCTTGATA	4067
rs756838222	in-del	-/C			intron-variant	LYN	GRCh38.p7	8:55886691	TGCAGGGGAATGTGG[-/C]CTGGAGCAGCTTTTC	4067
rs756842261	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55988791	TTTAGCTTTGCTTGA[A/G]AGATCACATTCAGCC	4067
rs756847071	snp	A/C			intron-variant	LYN	GRCh38.p7	8:56008830	TGGAACAGTTAACTG[A/C]GTCTGTGAAGTAGCT	4067
rs756879423	snp	C/T	0.000131796	0.00811668	synonymous-codon	LYN	GRCh38.p7	8:55947679	TGGCATCCACCCGGA[C/T]GACTTGTCTTTCAAG	4067
rs756885027	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55938006	CTGGCCAAGGTAAGA[C/G]TGATTTTTAAAAACC	4067
rs756938395	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55937009	TCTGACCCTCATAGA[C/T]ATTTATAGCTACTCT	4067
rs756969150	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55949847	TAGTCACAGAATTGT[A/G]CAATCATCACCACAA	4067
rs756976697	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55964823	TCTACCAGCCAGGGA[G/T]AATCACTGTTGTTTT	4067
rs756982541	snp	C/T	4.96553e-05	0.00498249	synonymous-codon	LYN	GRCh38.p7	8:55966881	CATTTACATCATCAC[C/T]GAGTACATGGCCAAG	4067
rs757077396	snp	A/G			upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55879071	GGCATTTATTGAGTT[A/G]AACATGAGCTTGAGC	4067
rs757081061	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55890432	AAAAATCAGAAAATA[A/T]TAAGTGGTGCCAAGG	4067
rs757101036	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55904447	CACCCTTTTTTCTGA[G/T]CATTTTTTCTGTTCT	4067
rs757149486	in-del	-/TTT			intron-variant	LYN	GRCh38.p7	8:55979051	ATGCACTTCTCATTC[-/TTT]TTTTTTTTTTTTTTT	4067
rs757155916	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55995543	GGGTTCATGTTCCTG[C/G]AGAAATTGTGGACAG	4067
rs757156499	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55915508	TCAGGAGTTTGAGAC[C/T]AGCCTGGTCAACATG	4067
rs757172762	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55990041	GTCAGGAGTTTGAGA[C/G]CAGCCTGGCCAACAT	4067
rs757302395	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55956442	TTAATGATGTTCTAT[C/T]TGATTTTATCTACAG	4067
rs757327685	snp	C/T	3.30289e-05	0.00406366	intron-variant	LYN	GRCh38.p7	8:55998517	ATGTTGCACTAATGA[C/T]CTTTAGATGTTTTAT	4067
rs757350283	in-del	-/CTT	1.65351e-05	0.00287528	intron-variant	LYN	GRCh38.p7	8:55954013	TCGGGGATCTATGTC[-/CTT]CTAGAGATGGTGACA	4067
rs757351733	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55991925	CAAAGAGCACAAGAA[A/G]CATCAGCACATCTCA	4067
rs757363979	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55887014	ATCCCCCCTTCCAAC[A/G]TACAGAGATGGGCAG	4067
rs757368307	snp	A/G			utr-variant-3-prime, downstream-variant-500B	LYN	GRCh38.p7	8:56011928	ATGGAGAGGAACTAT[A/G]AAGAATCCCTAAGGC	4067
rs757390567	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55912679	TTGCAGTGAGCCGAG[A/G]TTATGCCACTGCATT	4067
rs757417465	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55914022	GAAACAGGGGAGAGA[C/T]GAAATCATGGCTGCT	4067
rs757425561	snp	A/C	1.64825e-05	0.00287071	intron-variant	LYN	GRCh38.p7	8:55950597	TGGTGGCTTTATTTG[A/C]CACATTGGATTTCTT	4067
rs757428175	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55964778	AATCAGAATAGAAAA[A/G]AACAAGAGAAAGTAG	4067
rs757453100	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55969815	TATTCAAAAAGCCCC[A/G]TGTGCACGTGCATTT	4067
rs757486087	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55972205	GGGTCAGCAGCAGCC[A/G]GCAGGACCCTAAGTA	4067
rs757498066	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55999275	CAGTGAGCCGAGATC[A/G]CATCATTACATTCCA	4067
rs757501017	in-del	-/TATT	1.70055e-05	0.0029159	intron-variant	LYN	GRCh38.p7	8:55950818	CCTCTTTTAAAACAC[-/TATT]TAGGAAATTATTTTT	4067
rs757514007	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55953011	CTCGAAGGGGATGCA[C/T]ATTATAGGTTTGCTT	4067
rs757590224	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55938308	TGTCAAAGCCTCAGT[C/T]ACTATCTTGTTTTAA	4067
rs757598429	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55985979	CGAGACCCGCCTGGG[C/T]AATATAGTGAGACCT	4067
rs757600355	snp	A/G			intron-variant	LYN	GRCh38.p7	8:56000337	ATCAGTGAGGGCATC[A/G]TTCAGTATTTATTTC	4067
rs757605592	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55882670	TTACTGGCTCTTCCT[A/G]GTGATGATGGTGAAG	4067
rs757626226	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55915300	TTAAGCCTCTGCTAT[A/C]CAGGTTTATTTATAT	4067
rs757627379	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55886825	GTAAAGATTAAATCA[A/G]TATTTGCGATAGCCA	4067
rs757647394	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55987334	AATTGCTCGAGCCCC[A/G]GAGGTGGAGGTTACA	4067
rs757659694	snp	A/G	1.65644e-05	0.00287783	synonymous-codon, intron-variant	LYN	GRCh38.p7	8:55941886	AAAATCAAAAGGGAA[A/G]GACAGCTTGAGTGAC	4067
rs757675255	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55932329	AGTGACAGATTAATA[C/T]AGTTCTAAGAAGACT	4067
rs757696010	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55961180	TCCCTTTTGTGGTAC[A/G]TGGGCACTTTTTAGC	4067
rs757701782	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55959966	TGTCCAGAATAGGCA[A/T]ATCTAGAGTTAGAAA	4067
rs757716623	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55985883	TTTAATATACTAAGG[A/G]TGACCAGGCTCAGTG	4067
rs757716912	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55894166	AGTTTGCCTGTCTGC[A/G]TCCCCCAACCCCCCC	4067
rs757730106	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55943081	CTATTTGGTGTATTT[C/T]GGAAATACTTGGCAA	4067
rs757783193	in-del	-/G			intron-variant	LYN	GRCh38.p7	8:55889999	GCAAGTTGCTTAGCT[-/G]GGTGAAGTGGCTCAT	4067
rs757784361	snp	C/T	0.000221361	0.0105182	utr-variant-5-prime, missense	LYN	GRCh38.p7	8:55879946	GGGGCGGCCGCGCCA[C/T]CCCCGGCCCCGCGCC	4067
rs757788294	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55935717	ACCCAGGAGGCAGAG[G/T]TTGCAGTGAGCCGAG	4067
rs757789213	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55970669	ACGGCCTTCTTGGGA[A/G]TACGAGATCCAAGGA	4067
rs757806524	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55930513	TCTGCTTTGAATGTC[C/T]CCTTCTGGTCCTTTA	4067
rs757838398	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55987251	AACACCGTCTCTACT[A/G]AAATAAAAAAAATTA	4067
rs757839593	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55936892	CCTTTGATTACCTAG[C/T]ACAGGTTCATCTCTG	4067
rs757840780	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55898549	CTGCCTTGGCCTCCC[A/G]TAGTGTTGAGATTAC	4067
rs757895653	in-del	-/C			intron-variant	LYN	GRCh38.p7	8:55897437	TGCACATGGTGGTTT[-/C]GAGGGGTTGACAGCA	4067
rs757898869	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55887679	TGATGGTGTGATCTC[A/G]GCTCACTGCAACCTC	4067
rs757906580	snp	A/C	1.72121e-05	0.00293356	intron-variant	LYN	GRCh38.p7	8:55953790	ACAGGTAAAGTACAA[A/C]GTATTGCATTTCTTA	4067
rs757916294	snp	C/T	1.64751e-05	0.00287007	synonymous-codon	LYN	GRCh38.p7	8:55953920	AGATGCCTGGGAGAT[C/T]CCCCGGGAGTCCATC	4067
rs757972842	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55974730	AGAGATGTGTTAGAC[A/G]CTCATATTCCACCTC	4067
rs758002593	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55985746	AACTCTGCAGGCAAG[G/T]ACTGTTTAGTGGACC	4067
rs758014840	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55882490	ACTAACTTTATAAAT[A/T]AGGACACCATGTATA	4067
rs758017130	snp	A/T	8.24531e-05	0.00642026	synonymous-codon	LYN	GRCh38.p7	8:56010077	GGATGATTTCTACAC[A/T]GCCACGGAAGGGCAA	4067
rs758025228	in-del	-/G			intron-variant	LYN	GRCh38.p7	8:55903198	GGATTTCACCATGTT[-/G]GCCAGGCTGGTCTCG	4067
rs758033918	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55949100	TTCTGCTGAGGACTC[A/G]AGCATGGTGCTGAAG	4067
rs758052871	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55990036	CTGAGGTCAGGAGTT[G/T]GAGACCAGCCTGGCC	4067
rs758059771	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55887460	GTTTTTACTTCTGTA[C/T]GTCTTTATATTTAAA	4067
rs758064550	in-del	-/A			intron-variant	LYN	GRCh38.p7	8:55883923	GGTTTCCTGATACTT[-/A]AAATTGTGAAACTTT	4067
rs758084994	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55948100	CACCTCAGCCTCCTG[A/G]GAAGCTAGGACTACA	4067
rs758109163	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55959729	CATTATTTGTAATAG[C/T]CAAAAAGTACAAACA	4067
rs758140413	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55919448	AATACGCTTCACTGC[C/G]GGGTCTGGAAACCCT	4067
rs758270672	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55888868	AGCAAAATTTTAATA[A/T]GGAGTTTATGGTTGT	4067
rs758274526	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55915291	CAGATACCATTAAGC[C/T]TCTGCTATCCAGGTT	4067
rs758294298	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55925889	AAAACCAACTCACCA[C/G]AGAAGCATACAAGTG	4067
rs758304590	snp	G/T			utr-variant-3-prime, downstream-variant-500B	LYN	GRCh38.p7	8:56012076	TGCCATTTTCCACTT[G/T]TCTTTCCCTCCCAAT	4067
rs758327931	in-del	-/TA			intron-variant	LYN	GRCh38.p7	8:55942444	ATATGTGTGTGTGTG[-/TA]TATATATATATATAC	4067
rs758398043	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55992973	AATTTGGAGGGACAC[A/G]TTCAGACCATAGCAT	4067
rs758446641	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55952976	GAGTGGTTGTTGCCC[C/T]GGCTCCTTTCTATGA	4067
rs758485629	snp	C/T			intron-variant	LYN	GRCh38.p7	8:56004650	GCTCCTCAAAGTAAT[C/T]TACTTTTGGGAATTT	4067
rs758524919	in-del	-/CTCT	3.30218e-05	0.00406323	intron-variant	LYN	GRCh38.p7	8:55947730	CTGGAGGAGTAAGTG[-/CTCT]CTCTCAAGCACGCCA	4067
rs758549235	in-del	-/T			intron-variant	LYN	GRCh38.p7	8:55913073	TTTACTAGGTAAGTA[-/T]TTTTTATTACAAAGG	4067
rs758566806	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55912981	AATATTTAACCACTA[A/G]AAGAATTGATGATGC	4067
rs758567669	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55962798	ATGTTTATTTGCTTT[A/G]CGGTTCTTCAGATTT	4067
rs758571056	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55934970	AGTCACAGACAGGAG[C/G]TGACACCTAACCATC	4067
rs758608007	in-del	-/ACACACACACACACACACACACAC			intron-variant	LYN	GRCh38.p7	8:55909011	TATATATATATATAT[-/ACACACACACACACACACACACAC]ACACACACACACACA	4067
rs758623800	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55963782	TGTAAGAATTCTTTC[C/T]ATATCCTGGATGCAA	4067
rs758630449	snp	G/T	1.64808e-05	0.00287057	intron-variant	LYN	GRCh38.p7	8:55950603	CTTTATTTGCCACAT[G/T]GGATTTCTTGTTAAT	4067
rs758632671	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55885297	GTAGAACACTGGGAA[A/G]AAGTCTTCACAGCTC	4067
rs758632697	snp	C/T	3.29576e-05	0.00405928	synonymous-codon	LYN	GRCh38.p7	8:55999527	ATACGAAATTGTCAC[C/T]TATGGGAAAATTCCC	4067
rs758660191	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55997308	TTATTTGTATTAGCA[C/T]GTCACTTTCTCCAAC	4067
rs758672556	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55880952	TGTATATCCGAGTGT[A/G]TTAATTATCCCAAAT	4067
rs758712083	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55958581	CAGACTCTCTTTTCA[C/T]CTGATAAAACTGAGA	4067
rs758722511	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55995419	CCCTGTCCTTTTCCT[A/G]CTGTCCGTCTGGTTT	4067
rs758727543	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55892819	TATGTGTGTTTAAAA[C/T]TTAAGTATAACACTT	4067
rs758728428	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55957908	AGCTGAGATTGCGCC[A/G]CTGTCACCAAACTGG	4067
rs758763282	snp	C/T			intron-variant	LYN	GRCh38.p7	8:56002580	GCAGTCTAGCCTGAG[C/T]GACAGGAAGGAGACT	4067
rs758815145	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55998645	TAATTGTCTGCTTAT[G/T]GTTCTATTCTAATAG	4067
rs758836477	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55980333	AGGAGTTTTGAGCTG[C/G]TCCGCTTCTGACCTG	4067
rs758847770	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55970595	AAGACTGGTCCCTAT[A/G]GTCTTCCTTTTTCAC	4067
rs758866706	in-del	-/CTT			intron-variant	LYN	GRCh38.p7	8:55947504	CAGGAAGCACATGTC[-/CTT]CTTCCAGTTGCCCCC	4067
rs758903096	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55930426	GGATTGTTGATCATA[A/C]AAATCTGAATCTGGA	4067
rs758910062	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55901426	AACTGTTTAATTGAA[C/T]GGTTTCATCTCAAGG	4067
rs758919184	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55980124	ATGGTCTGCCCAGCC[C/T]TCCTCACTCATAATC	4067
rs758925814	snp	C/G/T	4.99591e-05	0.00499774	intron-variant	LYN	GRCh38.p7	8:55942023	AGGGGAGAATTCCCA[C/G/T]AGCAAGATCAAAGCA	4067
rs758940465	in-del	-/G			intron-variant	LYN	GRCh38.p7	8:55939745	ACGATTTTAAGGGAT[-/G]GTGAGTTAAACACCG	4067
rs758976253	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55940327	CCAGAGAATCTGTTC[A/G]GTGAGAACCAACTTC	4067
rs758995107	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55893823	TAGAAGCAAGATCTC[A/T]CTATGTTGCCCAGGC	4067
rs759005289	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55932399	AAATCTTTTAAAACA[A/G]TTATATATATATTTT	4067
rs759027092	snp	A/T			upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55878043	TCTAGTTTAAAATAA[A/T]GTTGCACACCATACA	4067
rs759052252	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55902973	CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA	4067
rs759063977	snp	C/G			downstream-variant-500B	LYN	GRCh38.p7	8:56012526	CTCAGGAGTTAGACA[C/G]CAGCCTGAGCAATAT	4067
rs759091791	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55882131	TCTCCACTCAGCACC[A/G]CTCTTCTCTACTTAT	4067
rs759106426	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55971084	ATCCTCTCCACCTCC[A/G]GGACTTGGCAAGCCT	4067
rs759167118	in-del	-/TGAC			intron-variant	LYN	GRCh38.p7	8:55958673	CTGTCTCTATGAATT[-/TGAC]TACCTTAGGTACCTC	4067
rs759181452	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55991102	ATAGTGGCCTCTGAG[A/T]TGCTGCTCGGGGTCT	4067
rs759181720	snp	A/C	1.64849e-05	0.00287092	synonymous-codon	LYN	GRCh38.p7	8:55966839	CAAGCTCGTGAGGCT[A/C]TACGCTGTGGTCACC	4067
rs759193421	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55970546	TCATGAAGCCCAGTG[G/T]ATGTAGCAAAAGAGA	4067
rs759218102	snp	A/G			intron-variant	LYN	GRCh38.p7	8:56000707	CACTCTAGCCATGGC[A/G]ACAGAGTGAGACTCT	4067
rs759233831	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55942603	CAGCCTGGCCAACAT[A/G]GTGAAACCCCATCTC	4067
rs759252804	in-del	-/GC			intron-variant	LYN	GRCh38.p7	8:55911680	GCAGTCCTATGAGCT[-/GC]GCGGGGCACCTGCCC	4067
rs759282657	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55941167	TGCCCTTGAAGTCTC[A/G]AGGCCCCCCACCCCA	4067
rs759312061	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55896682	AAAAAAAGAAACATA[A/G]AATAAAAACCATACC	4067
rs759334958	snp	A/G	1.64991e-05	0.00287215	intron-variant	LYN	GRCh38.p7	8:55998504	AGCAAGGGAAGGTAT[A/G]TTGCACTAATGATCT	4067
rs759346878	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55921284	TTGTTGCTGACTTGG[G/T]AACCAGGTGGCCCAC	4067
rs759384268	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55951518	AGAAATTAAAAAATT[A/T]GCCAGCTGTGGTGGT	4067
rs759439443	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55960843	AGTGACCTGTTCTTT[C/G]GGGGAAGGGGCTGGG	4067
rs759456616	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55977058	GGCATGGTGGTGTGC[A/G]CCTGTAATCCCAGCT	4067
rs759482637	in-del	-/AGAG			intron-variant	LYN	GRCh38.p7	8:55939464	TTTTCCCAAGAGAAG[-/AGAG]AGAGAGAGAGAGAGA	4067
rs759490344	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55959710	ACATGAGTGTTCATA[A/G]TAGCATTATTTGTAA	4067
rs759491091	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55987211	TGAGATCAGGAGTTC[A/G]AGACCACACTGGGGA	4067
rs759526372	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55920498	CATTTAACATATGCT[A/G]TTTCATTTAATCCTC	4067
rs759536130	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55914561	CTGCCGGCCATCCAC[A/C]TGCCTTCCAGGAACA	4067
rs759543766	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55884517	GCTGGAGTGCTTTGG[C/T]GTGATCCCAGTTCAC	4067
rs759548882	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55949078	CTCCCTGGCTCCATG[C/G]CTGCCTTTCTGCTGA	4067
rs759549120	snp	C/T	1.64751e-05	0.00287007	synonymous-codon	LYN	GRCh38.p7	8:55999464	AGAAGCAATCAACTT[C/T]GGATGTTTCACTATT	4067
rs759611364	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55983994	AGAATCCTTCCGTAC[C/T]TCTTCCAGCTTCTGG	4067
rs759674975	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55896719	AGTAAGAGAGGCATT[A/C]CCCCCAAGCTCCTCA	4067
rs759684313	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55916411	TCAATTTCTTCTGGA[C/G]TTTGTCAGGTTACTT	4067
rs759691111	snp	A/G			upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55878869	TATTGCTCTGTAGCT[A/G]GGGTCAGCCTCTTCA	4067
rs759727456	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55905928	CATCTTGACTTCTGG[A/T]AAGAAGCCTATAGTG	4067
rs759730549	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55934712	ATTCAGACCCAGAGA[C/T]ATCCCTCCTGTGTTG	4067
rs759756824	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55917297	CTCATGTGATCGTCC[C/T]GCCTCAGCCTCCCAA	4067
rs759809889	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55928548	GGTGAGGTGTCTATT[C/T]AGATCTGTTGCCCAT	4067
rs759811147	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55957949	GAGACCCCATCTCAA[A/T]AAATAAATAAATAAA	4067
rs759824481	snp	A/G	9.92572e-05	0.00704406	missense	LYN	GRCh38.p7	8:55952094	TTTCCCTGTATCAGC[A/G]ACATGATTAAACATT	4067
rs759861985	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55992328	GCTGAGGCCTGACCC[G/T]GTATCCCCTGCCTCC	4067
rs759887403	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55913547	CCAGTGCTGGAGGAG[A/G]TTTTTGAGGGGTTGA	4067
rs759912691	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55953413	GCATTTTGGGAGGCC[A/G]AGGCGGGTGGATCAC	4067
rs759940265	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55912546	GCCTGGCCAACGTGG[A/C]GAAACCCCGTAGCTA	4067
rs759963554	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55886538	CAGGCATGAGCCACG[C/T]GCCCAGCCTGTCAAA	4067
rs759963862	snp	C/G			intron-variant	LYN	GRCh38.p7	8:56005690	TTTTGGGATGAATTA[C/G]AGAAAAAAGAAAATA	4067
rs759978576	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55935452	AAAGACGGTCTGGCT[A/G]GGTCCTTTTCAGTTC	4067
rs759989796	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55979804	CTCTCTGCCAAGCAG[C/T]AGCCTGACACCCTGC	4067
rs759990855	snp	C/T	1.64746e-05	0.00287002	synonymous-codon	LYN	GRCh38.p7	8:55947661	AGCCTTGTACCCCTA[C/T]GATGGCATCCACCCG	4067
rs759998312	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55925370	CTCAAGCAGTCCTCC[C/T]GCCTCACCTCTGAAA	4067
rs759999507	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55924419	CCAGGCTGGAGTGCA[A/G]TGGTGTAATCTTGAC	4067
rs760178002	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55897296	TTAAGAACAGTAAAG[C/T]TTTCTCTGTTGTACC	4067
rs760195354	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55991606	AGAACCCCCCACCCC[C/T]AGGATTTGCTCTCTG	4067
rs760201237	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55912499	GGAGGTCGAGGCAAG[C/T]GGATCACCTGAGGTC	4067
rs760222750	in-del	-/AT	1.64741e-05	0.00286998	intron-variant	LYN	GRCh38.p7	8:55969799	TTCTGCTCAGGTAAC[-/AT]ATTCAAAAAGCCCCG	4067
rs760230565	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55980963	CTAGCCCCTGGCCAC[A/C]CCCGTGCTGTTCTCG	4067
rs760230695	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55969498	CCACATTCTTTCTCA[C/T]CTGGAGCACATGCCA	4067
rs760240501	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55896664	TATAATAAAAAAATT[A/T]TAAAAAAAAGAAACA	4067
rs760246078	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55902760	ACCACTGCAATATGC[A/C]TACTGTGATGGAAGC	4067
rs760247722	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55892477	AAGGTGCTTCCTGAT[G/T]TGATGATACAGTTAT	4067
rs760282052	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55927960	GGGTCATATGGTAAG[A/G]GTATTGTTTAGTTTT	4067
rs760301322	snp	C/T	9.88452e-05	0.00702942	missense	LYN	GRCh38.p7	8:55947675	ATGATGGCATCCACC[C/T]GGACGACTTGTCTTT	4067
rs760374679	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55964236	TTCTTTTCTTTTTTT[A/G]TTTTGTTTTAGAGAA	4067
rs760381512	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55985379	GAGCAGACGTCACAG[G/T]CTTCCCTCGCAAACA	4067
rs760383864	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55886491	GACCTCAGGTGATCT[A/G]CCTGCCTCGGCCTCC	4067
rs760384210	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55911839	TTTAAACTTCAGCAC[C/T]TGGTGCCCTTTACTG	4067
rs760409755	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55881914	GATTACTTGGAAGAA[A/G]GAATGAAGGCCTCCT	4067
rs760434036	snp	A/G	1.64751e-05	0.00287007	intron-variant	LYN	GRCh38.p7	8:55969713	GTTCTTTCTTTCTCC[A/G]TAGGCAGTTTGCTGG	4067
rs760438345	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55914098	GTGGAGGGTTGTTGT[C/T]GGTGTGTGTGTGTGT	4067
rs760443176	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55995055	GGGTTACCAGCAGAC[A/T]AAAGGAAACAGAGGC	4067
rs760471477	snp	C/T			utr-variant-3-prime	LYN	GRCh38.p7	8:56012279	TAGGTGTTTGTAGCA[C/T]TTTCGGGTATCCAGT	4067
rs760473420	snp	A/G	1.65157e-05	0.0028736	missense	LYN	GRCh38.p7	8:55950730	GAAAGGCAGCTTTTG[A/G]CACCAGGAAATAGCG	4067
rs760507497	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55934210	CAGCCTGGGCGACAG[A/G]GCGAGATCCGTCTCA	4067
rs760513950	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55959360	GATTTACTAATAACG[C/T]TTTAAATGACAGAGG	4067
rs760527134	in-del	-/T	1.69275e-05	0.0029092	intron-variant	LYN	GRCh38.p7	8:56009891	TTTCTGTTCTTTTTG[-/T]TTTTTTTCCACCCTA	4067
rs760534916	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55997708	CATCTGTTTTCTGAT[A/T]TGAGAAACTGGCATA	4067
rs760542127	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55999787	GACCAGACTGACCAA[A/C]ATGGAGAAACCCCGT	4067
rs760568071	in-del	-/TT			intron-variant	LYN	GRCh38.p7	8:55939234	GGGGACCCCAAACAC[-/TT]TGTGAGCAGAGATCA	4067
rs760593090	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55880760	TTTTGCCGGCTGAGA[G/T]GAAGCGAGAGTTATT	4067
rs760593456	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55986574	TCTCTCCCTAAGGCA[C/T]TGTGGGTCCTTGCAT	4067
rs760615092	in-del	-/T	6.7348e-05	0.00580254	intron-variant	LYN	GRCh38.p7	8:55946521	GCAACATAGTTAAAA[-/T]TTTTTTTTCTTTACT	4067
rs760620068	snp	A/G	1.73975e-05	0.00294931	intron-variant	LYN	GRCh38.p7	8:56009874	GTTTCTAAACGGCAT[A/G]GGTTTCTGTTCTTTT	4067
rs760621957	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55893722	GCAAAACTGTTCCAG[A/T]TATACTCAGAGAGTT	4067
rs760630083	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55998033	AGCTTGCAGTGAGCC[A/G]AGATAGCGCCACTGC	4067
rs760637025	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55982166	CACCCAGCGCCCCCA[G/T]TGTCTGTAACATCAT	4067
rs760695307	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55882104	CATTTAGTGTGGGTA[A/G]CTAAATGAGAGTCTC	4067
rs760731285	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55995251	CTCTGCCTTCACCTG[A/G]TTATCACCACTGCCC	4067
rs760786385	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55996351	TGGTCTGGAACTGGC[A/G]GCCTGAAGTGCTTGA	4067
rs760823636	snp	A/C			intron-variant, downstream-variant-500B	LYN	GRCh38.p7	8:55968033	CTGTGAGTATTTCAA[A/C]ATATCAGTCACTCAG	4067
rs760840076	snp	A/G	1.6519e-05	0.00287388	intron-variant	LYN	GRCh38.p7	8:55954003	AGTGTGCGGCTCGGG[A/G]ATCTATGTCCTTCTA	4067
rs760884122	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55889757	TAAGGCAGGGCAGGG[C/T]GGTAGAGCACAGGGT	4067
rs760888367	snp	A/G			intron-variant	LYN	GRCh38.p7	8:56004766	TTATTAGATAAGGAT[A/G]TGGCCACATACTTTT	4067
rs760889985	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55916256	TTGAGGGGAAAGTGA[A/G]TATTGAGAAAAAATA	4067
rs760894198	snp	C/T	1.64928e-05	0.00287161	synonymous-codon	LYN	GRCh38.p7	8:55953872	ATTGGAGAAGGCTTG[C/T]ATTAGTCCCAAGCCA	4067
rs760937081	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55956119	TGCTCATTAAAAAAA[A/G]AATGACTTGGCTTCT	4067
rs760967804	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55938546	AGAAAACCTAGGGCA[A/T]ATGTGCAGGTCAGTT	4067
rs760989501	snp	A/T	1.66852e-05	0.0028883	intron-variant	LYN	GRCh38.p7	8:55941834	TGGTAAAACAATGTC[A/T]TTACTTTTATGTTTC	4067
rs760996985	snp	A/C	3.29549e-05	0.00405911	synonymous-codon	LYN	GRCh38.p7	8:56010023	CTGGAAAGAAAAGGC[A/C]GAAGAGAGACCAACG	4067
rs761024742	in-del	-/CACC			intron-variant	LYN	GRCh38.p7	8:55962827	TTATAAGAAGCATGG[-/CACC]CACCTGTCTCTGCTT	4067
rs761068719	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55920360	TTTAACAATTTTGTT[C/T]GTGCAGAATGTCACA	4067
rs761082959	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55935325	CCCGGGTTACCAGCT[C/T]ACCAACTGTGCCCAC	4067
rs761098275	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55966325	CTTTTTCTATCTGTA[A/G]TTAAATTTTTTGCTA	4067
rs761138866	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55990527	TTTCCCCCATAAGAG[A/T]TGGCTTTGCAGGGCC	4067
rs761182646	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55963529	AAGAACACAGAATGA[A/G]GCCTAGGGCAGCTGC	4067
rs761183636	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55905862	CCCATGCAAAGAGCC[C/T]GCTCCTCTGTTCCTG	4067
rs761193068	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55945768	GATGCCATCTGTCCC[C/T]GTGATGGAGTCAGGG	4067
rs761195925	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55983950	TGGAATGAAGGTATA[A/G]GCAGGGCTGTGCTTC	4067
rs761246309	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55894735	AGACGGGGTTTTGCC[A/G]TGTTGGCCAGGCTGG	4067
rs761252044	snp	A/G	8.29222e-05	0.00643849	intron-variant	LYN	GRCh38.p7	8:55947755	ACGCCACGGCTGCTC[A/G]TTTCCTCAGGCCACT	4067
rs761253224	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55973343	ATCCATAGCCCATTC[A/G]ACATAGATCAAGAAA	4067
rs761264151	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55889488	GCTGGGATTACAGGC[A/G]TGAGCCACCACACCC	4067
rs761302512	snp	C/T	1.64822e-05	0.00287068	intron-variant	LYN	GRCh38.p7	8:55969841	CATTTGCAAAGACTT[C/T]CCTGCGTCAAATTCA	4067
rs761336342	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55885482	CAGTCCCCGCTTTCC[A/T]CCCTCCATTGGTAAA	4067
rs761353837	snp	A/T	5.16258e-05	0.00508038	intron-variant	LYN	GRCh38.p7	8:55950827	AAACACTATTTAGGA[A/T]ATTATTTTTAGAAAC	4067
rs761355488	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55970756	GTAATAGAGCATCGT[A/G]GGCTAAGCTGGCATT	4067
rs761393842	snp	G/T			intron-variant	LYN	GRCh38.p7	8:56001994	CATTTTTTGAAAAAA[G/T]AACTGGCTGGGCACG	4067
rs761396898	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55968896	GGTCTTGCTTTAGAG[A/T]TGAAGCCATAGGAGG	4067
rs761404093	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55900838	TTAAGGAGAATAGCT[C/T]TTGGAAATCTTATAT	4067
rs761407123	snp	C/T	1.6625e-05	0.00288309	intron-variant	LYN	GRCh38.p7	8:55947766	GCTCGTTTCCTCAGG[C/T]CACTGAGTCCTGCAG	4067
rs761434964	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55978192	GGGATAATGGGGATC[A/G]ACTGAGCATTTCAGC	4067
rs761460854	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55911721	GGCAGGGAGTCAAAG[C/T]GACATGAGATTGGGG	4067
rs761466016	in-del	-/T	6.67858e-05	0.00577827	intron-variant	LYN	GRCh38.p7	8:55946417	AAAAGCTAAACAGAA[-/T]TTTTTTTTTCTAACA	4067
rs761492860	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55880734	CGGCCTGCCGAGGAG[A/C]AGTCCGGTGCTTTTG	4067
rs761496837	in-del	-/GAGAGC/GAGC			intron-variant	LYN	GRCh38.p7	8:55939487	AGAGAGAGAGAGAGA[-/GAGAGC/GAGC]ACGCTGGAGCGAGCA	4067
rs761545304	snp	A/G	1.64808e-05	0.00287057	synonymous-codon	LYN	GRCh38.p7	8:55998417	AGCAGCTAATGTTCT[A/G]GTCTCCGAGTCACTC	4067
rs761545730	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55892415	ACAGAGCAAGACTCC[A/G]TCTCAAAAAAATAAA	4067
rs761551788	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55984336	CGTGAGCCCCTGCTG[A/G]CTCAGCATCTGCCCA	4067
rs761562508	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55934354	CTTCCATCATTACTG[C/T]TTCTTCTTCTTACCC	4067
rs761570475	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55917399	ATGTTGCCCAGGCTG[A/G]TCTTGAACTTTTGGA	4067
rs761570932	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55921887	ACAGATATTTACAGA[A/G]CATTTACAAGTGCCG	4067
rs761574986	in-del	-/C			intron-variant	LYN	GRCh38.p7	8:55987406	AGTGAGACTTCATCT[-/C]AAAAAAAAAAAAAAA	4067
rs761611407	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55979581	AAAAACTGAGTCACC[A/G]AAAGTAGCCCTTGCC	4067
rs761614720	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55881808	ATAGTCTGTATTAAC[C/T]ATTACAGTGGAAGCT	4067
rs761631336	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55933017	ATTTGGTACTATGCT[C/T]ACTACCTGGATGGTG	4067
rs761666621	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55969127	CTCTACAAAAAAAAG[A/G]ATTAGCTGGGTGTGA	4067
rs761691451	snp	A/G			utr-variant-3-prime	LYN	GRCh38.p7	8:56011215	GACTACAAGGCTCTA[A/G]TAAGCCACGGTGGCA	4067
rs761704614	in-del	-/CAA			intron-variant	LYN	GRCh38.p7	8:55942784	AACAAGACTCTGTCT[-/CAA]AAAAAAAAAAAAAAA	4067
rs761759409	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55939829	ACTCCCATGCTTACT[C/T]AGAGATCAACTCTAA	4067
rs761768405	snp	C/T			intron-variant, downstream-variant-500B	LYN	GRCh38.p7	8:55968289	GAGACAGAGTCTCAC[C/T]CTATCACCCAGGCTG	4067
rs761779641	snp	C/T	1.65059e-05	0.00287275	missense	LYN	GRCh38.p7	8:55952085	CGAATCACTTTTCCC[C/T]GTATCAGCGACATGA	4067
rs761788902	snp	A/G			intron-variant	LYN	GRCh38.p7	8:56007441	TATTTTAGTTAGAAA[A/G]TTCTAGTCACACAAA	4067
rs761838069	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55993647	CCTGGTCAATTTGCT[A/G]TTAAGATGAAACATG	4067
rs761841026	in-del	-/TT			intron-variant	LYN	GRCh38.p7	8:55919950	CACGTGACCCCACTC[-/TT]TGCTTCTTTGTCTGT	4067
rs761860567	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55966969	GTGTAAGTGTTCAGA[A/G]GTCACTCAACTAGTT	4067
rs761961592	snp	A/G			upstream-variant-2KB	LYN	GRCh38.p7	8:55877091	TTCTGTTTAATGGAC[A/G]CCTTATTTAATATAT	4067
rs761963418	snp	C/T			intron-variant	LYN	GRCh38.p7	8:56004410	GCAATGCTCCTGCCT[C/T]AGCCTCCTGAGTTGC	4067
rs762013066	snp	C/T	1.64808e-05	0.00287057	synonymous-codon	LYN	GRCh38.p7	8:55966812	CAACCTCATGAAGAC[C/T]CTGCAGCATGACAAG	4067
rs762013082	snp	G/T	8.31677e-05	0.00644802	intron-variant	LYN	GRCh38.p7	8:55942014	GATAGTCTCAGGGGA[G/T]AATTCCCACAGCAAG	4067
rs762029441	snp	A/G	4.99563e-05	0.00499756	synonymous-codon	LYN	GRCh38.p7	8:55946468	AGAATCTCAGCTTTT[A/G]CCTGGACAGAGGTTT	4067
rs762031809	snp	C/G			intron-variant	LYN	GRCh38.p7	8:56006093	TGTCTCAAAAAAAAG[C/G]TGGGGGTGTCTTGTT	4067
rs762039929	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55898382	CAACCTCCGCCTTCC[A/G]TGTTCAAGCAATCCT	4067
rs762051388	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55978739	GACGGAGTTCTGACA[C/T]GCAGTCAGAGAGCAG	4067
rs762053359	in-del	-/AAAAAAAAT			intron-variant	LYN	GRCh38.p7	8:56008125	TCTGCCTCAAAAAAA[-/AAAAAAAAT]AAATAAAATAAAATA	4067
rs762092016	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55937548	ACATCCTTATGCCCC[G/T]GTGCAGTGTATTTAA	4067
rs762114956	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55949607	TCATGGGATACAGAG[C/T]GATATTTTGATACAT	4067
rs762147434	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55936623	CCAGCCTGGGTGACA[C/G]AGTGAGACTCCATCT	4067
rs762154707	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55895791	AGGATTAAACGGGGT[A/G]ATGTACCTGGGAGTT	4067
rs762157717	snp	C/T			intron-variant	LYN	GRCh38.p7	8:56001623	AGATTAATGAATTAA[C/T]ATTGCTGCAAAATAG	4067
rs762202479	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55907815	AGGCTGCAGTGAGCT[A/G]TAATAGGGCCACTGC	4067
rs762209815	in-del	-/A			intron-variant	LYN	GRCh38.p7	8:55971161	CCAACATCTAATAAG[-/A]AAGAAGCATAATTGC	4067
rs762303382	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55933771	GTTCTAGATGCCAAT[C/T]TTCCATATACCTCTT	4067
rs762329725	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55915958	CATGAGTATGTTTCT[A/G]TTTTAATACCTCTAA	4067
rs762334449	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55955976	TGAATAATGCTGTAT[G/T]AATGTTCACATACAA	4067
rs762405909	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55939056	TATCACTTGGAACAT[A/G]TAACCACTCTCAGTT	4067
rs762406207	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55883504	CTGCTAAGATGACAC[A/C]TATACTGGCTGCTGT	4067
rs762440691	snp	A/G			intron-variant	LYN	GRCh38.p7	8:56001198	GCCAACAGGAGCAGG[A/G]GGCCAGCGTGGTTTG	4067
rs762476570	snp	A/G			utr-variant-5-prime	LYN	GRCh38.p7	8:55877721	GCCTTCTCTTGCCCC[A/G]CCCATCGTATTCCTT	4067
rs762505785	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55884466	TTTTTTATTCTGCCT[C/G]CCACTGAAGAGACAG	4067
rs762523080	in-del	-/C			intron-variant	LYN	GRCh38.p7	8:55906698	GGCAACGTAGCAAGA[-/C]CCAGTCTCTACCAAA	4067
rs762529077	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55944368	AAATTAGAGTCACAA[A/G]TAGTTTTCTTATAGA	4067
rs762556578	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55895726	ATGTTTTTCTAATAC[A/G]TAAAACAGTAATAAC	4067
rs762570778	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55892093	TAAATGTTTGTCAGC[A/G]AAGGCTAAGAGATTC	4067
rs762589302	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55962129	GTGGCTACAGTTCAT[A/T]CATCTTCATTCCATG	4067
rs762600816	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55921398	GAGAGAGCTATACAC[A/G]TACTAACTGATAGAC	4067
rs762632659	snp	A/G			intron-variant	LYN	GRCh38.p7	8:56008391	ATGGAAAGGAAATTC[A/G]TTGTGAGGAATGGAG	4067
rs762653860	in-del	-/C			intron-variant	LYN	GRCh38.p7	8:55945445	TGGGTTTTTCTGGTA[-/C]TACAATGTAGTAATT	4067
rs762655883	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55933419	CAGTCCCACAATAAG[C/T]ATTCTCTTGTATAGA	4067
rs762659832	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55880907	ACTTTCCAACAGCCT[G/T]CCTGTCATGTGGATT	4067
rs762698148	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55900365	GGAAAAATAATCTTC[C/T]TCTTTTTTATTTTTA	4067
rs762706949	in-del	-/CAGGGCA			intron-variant	LYN	GRCh38.p7	8:55956385	GCAGTACTGTGTTCT[-/CAGGGCA]CCTGTCAGGAGGCAT	4067
rs762709024	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55932191	TAATAAAAGATGACA[G/T]TAAGGTTGAAGAATT	4067
rs762709390	snp	C/T	6.7228e-05	0.00579737	intron-variant	LYN	GRCh38.p7	8:55998309	TTTCCAGTCACCTAC[C/T]CTACATATGAAAATG	4067
rs762718496	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55927902	TTTTGTGTGTACATA[C/T]GTTTTCAACTCACTT	4067
rs762747423	in-del	-/TT			intron-variant	LYN	GRCh38.p7	8:55979052	TGCACTTCTCATTCT[-/TT]TTTTTTTTTTTTTTT	4067
rs762766464	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55889964	TGGCTAAATGGTAGT[C/T]ATTGGTATTGTTATC	4067
rs762775113	in-del	-/TA			intron-variant	LYN	GRCh38.p7	8:55942267	GCAAAGACCCCACTA[-/TA]TATATATATACACAC	4067
rs762797392	snp	A/G	3.29603e-05	0.00405944	synonymous-codon	LYN	GRCh38.p7	8:55998426	TGTTCTGGTCTCCGA[A/G]TCACTCATGTGCAAA	4067
rs762797558	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55939672	GCTCCTGCCCCGGAG[C/T]TCGCGGCGTGCGCAG	4067
rs762802401	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55978016	CAATTCAGAGCTAGA[C/T]TCTCAGGCCCTCTCC	4067
rs762846407	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55938747	TGGCATTGTTAATAA[A/G]TAGATGAAACATGCA	4067
rs762882622	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55888790	CATCCAGGCTGGAGT[A/G]CAGTGGTACGATCTC	4067
rs762888380	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55899425	TGTGGAACATAATGT[C/T]CTTGACTTTAGTTTA	4067
rs762899320	snp	A/G			intron-variant, downstream-variant-500B	LYN	GRCh38.p7	8:55968179	AGTTCAGTAAATATT[A/G]TTGAATTAATTAACT	4067
rs762905324	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55940281	AGCAGCATGCTCCCA[C/T]TGTGCCCCAGAAGAG	4067
rs762959855	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55975964	GTGGTGGTGCTTTTG[G/T]CCTGCAGGCAAGATC	4067
rs762970874	snp	C/T			intron-variant	LYN	GRCh38.p7	8:56005957	GAGTATGGTGGTACG[C/T]ACCTGTAGTCTCAGC	4067
rs762985514	in-del	-/TTT			intron-variant	LYN	GRCh38.p7	8:55890728	ATATGTACATTGGAA[-/TTT]TTTTTTTTTTTTTTT	4067
rs763001972	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55936545	CCTGGGAGGCTGAGG[C/T]AGAAGAATTGCTTGG	4067
rs763077755	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55964610	AGTGGCTCATGCCTA[C/T]AATCCCAGCACTTTG	4067
rs763091093	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55906073	GATATGTGCAGTTAC[A/G]CAGCACCTGTTAAGT	4067
rs763101290	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55998223	ACTGTCTTTAAAAGC[G/T]GAATGATCAAAATAG	4067
rs763115807	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55886662	ATCTGGTGGAACAGC[C/T]CCTCCCCTTAACTTG	4067
rs763145377	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55942503	TCAAGATAGTAGTGA[C/G]AGGCTGGGCGCGGTG	4067
rs763145713	snp	A/T	6.59044e-05	0.00574002	missense	LYN	GRCh38.p7	8:55947636	CAGAGGAACAAGGAG[A/T]CATTGTGGTAGCCTT	4067
rs763166264	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55974164	TGGGACTTGATCCAG[G/T]GACTTCTGACTCAAG	4067
rs763166696	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55897398	CAGGAGGGAGCATTC[C/T]GACGCTGAGCACACC	4067
rs763178527	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55963334	AGATTCTCACCAGCA[A/G]TATGCCAGTCCCCAC	4067
rs763182218	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55985271	GCAAAATGCTTGACC[G/T]TGCTTCTTCCTCAGC	4067
rs763183655	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55903587	TCATTTCCTGGAAGG[A/G]TATTTTTCACTGTAA	4067
rs763191524	snp	A/G			intron-variant	LYN	GRCh38.p7	8:56001102	GGTCCTGGCAGCAGC[A/G]GGGACTCACAGAGGG	4067
rs763239868	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55918558	GACAGATCTAGAAAC[A/G]ATTGTTAAGGAATAA	4067
rs763277260	in-del	-/G			intron-variant	LYN	GRCh38.p7	8:55994113	TAGCCGTAGTAAATA[-/G]ACCACCTTCAACAAC	4067
rs763294733	snp	C/T	1.70662e-05	0.00292109	intron-variant	LYN	GRCh38.p7	8:56009885	GCATGGGTTTCTGTT[C/T]TTTTTGTTTTTTTCC	4067
rs763344428	snp	A/G	3.35621e-05	0.00409633	intron-variant	LYN	GRCh38.p7	8:55946512	TGTTTTCATAGCAAC[A/G]TAGTTAAAATTTTTT	4067
rs763357103	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55914656	CAGAATGGCCATAGT[C/G]GTGATTATGTTCCTT	4067
rs763388666	snp	C/T	4.9445e-05	0.00497193	synonymous-codon	LYN	GRCh38.p7	8:55966830	GCAGCATGACAAGCT[C/T]GTGAGGCTCTACGCT	4067
rs763392524	snp	C/T			utr-variant-3-prime	LYN	GRCh38.p7	8:56011004	AGAACCTTATAGGGC[C/T]TTCTAAAACATAAGA	4067
rs763401335	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55913846	GAAGCAAGCAAGTGC[A/G]AGGGCACCAGAAGGT	4067
rs763415828	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55965587	AACAAAATTAAAATC[G/T]CTCGTAATCACACCA	4067
rs763422799	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55904959	GAGCATTTAAACCTC[A/C]CCATGCCCAAGCTGT	4067
rs763445467	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55942951	CAAAATAGTACAGAT[A/C]CTGAAGTTGTCATCT	4067
rs763445535	snp	A/T	5.57564e-05	0.00527969	intron-variant	LYN	GRCh38.p7	8:55966671	CCTCCCCCGGCTAGA[A/T]TTTCTGTTTTATAAA	4067
rs763463666	snp	A/T			intron-variant	LYN	GRCh38.p7	8:56007177	GGAAGGAAGTGAAAG[A/T]GATATTCCAAACTGA	4067
rs763476089	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55926349	GCAGGATTAGTAAAC[A/G]CTGATAAAGGCCTGT	4067
rs763487786	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55888115	CTTAAAGAACCTTCC[A/G]CTGCTATGTTTAGTA	4067
rs763554883	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55937944	TCAGATGATCCACCC[A/G]CCTCGGCCTCCCAAA	4067
rs763609345	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55949800	ATACAATCCATCTAC[A/T]TAAAGTGTACAATTC	4067
rs763666369	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55908621	ATACAATATTAAGAG[A/G]TGCAAGTGCAGTTTT	4067
rs763682770	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55932765	ATACTCGCATTTATA[A/T]ACCAGGGAATACTAC	4067
rs763691359	in-del	-/A			intron-variant	LYN	GRCh38.p7	8:55944158	ATGATGTTTCTTGAT[-/A]AATTAACATTGTAAT	4067
rs763702124	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55992762	GGCGCCAGTAGATAC[A/G]GTGCCTGGCGAGGTA	4067
rs763714022	snp	C/T	1.65957e-05	0.00288055	intron-variant	LYN	GRCh38.p7	8:55947760	ACGGCTGCTCGTTTC[C/T]TCAGGCCACTGAGTC	4067
rs763733717	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55961008	CTAAGGACGATGTTT[C/T]CTCTGACTGCTTGGT	4067
rs763741126	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55928753	TGAAGTTCAATTTAT[A/G]ATTTTTTCTTTCATG	4067
rs763743402	snp	C/G			missense	LYN	GRCh38.p7	8:56009993	AGATGAGCTCTATGA[C/G]ATTATGAAAATGTGC	4067
rs763788714	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55909428	TTCTGACTTGGACAT[C/G]TTCAGTCATAATCCC	4067
rs763789317	snp	A/G			intron-variant	LYN	GRCh38.p7	8:56001206	GAGCAGGAGGCCAGC[A/G]TGGTTTGGGCCTCTG	4067
rs763804697	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55996725	CTTCCTTAAAAACCT[G/T]ACTTTGGAACGATAC	4067
rs763827458	snp	C/T	1.65116e-05	0.00287324	synonymous-codon	LYN	GRCh38.p7	8:55966866	CACCAGGGAGGAGCC[C/T]ATTTACATCATCACC	4067
rs763893790	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55916463	CATACATAATACTGC[C/T]CTGGAAGGGTGCGTG	4067
rs763968605	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55899996	TTGCCAATGTCATGT[C/T]ACTGTACGAGGTGGA	4067
rs763985380	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55890274	CAATGATTACACCAC[A/C]ACACTCCATCCTGGG	4067
rs764089964	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55927903	TTTGTGTGTACATAC[A/G]TTTTCAACTCACTTG	4067
rs764102106	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55912651	AGACTCTCTTGAACC[C/T]GGGAGGCAGAGGTTG	4067
rs764135091	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55964625	CAATCCCAGCACTTT[A/G]GAAGACCAAGGTGAG	4067
rs764175485	snp	A/G	1.66685e-05	0.00288686	intron-variant	LYN	GRCh38.p7	8:55941843	AATGTCATTACTTTT[A/G]TGTTTCAACAGGAAA	4067
rs764223561	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55991803	ACCGCTTTTTAAAAA[C/T]GAAAATGAAAAACAC	4067
rs764255244	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55907125	GGTCCACAAAAAGAC[A/G]TGTCCAGTTCTATAT	4067
rs764255618	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55963619	AATTTTTGCTGAGCT[C/T]GGCAGTGGTTTCTCA	4067
rs764267394	snp	A/G			intron-variant	LYN	GRCh38.p7	8:56004660	GTAATCTACTTTTGG[A/G]AATTTTGATTCCTTA	4067
rs764269304	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55915181	TTGCAGCTGTCCAAC[C/T]TCTCTGGCATTCTAG	4067
rs764270516	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55992690	GCTTTCAAGCCTATG[A/G]TCTAGTGCTCTGCTT	4067
rs764340056	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55886781	ATAGTTTCAGGGCAC[A/G]TGTGATAATTTAATA	4067
rs764341816	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55940297	TGTGCCCCAGAAGAG[A/T]TTCCCGGACAGTGTC	4067
rs764366072	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55974457	AACTCTATCTAGGAA[A/G]TTCTCGACCTTTTTG	4067
rs764378360	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55894102	GTCACAAGTGAAGTC[C/G]TGGCCATGCAAGGAA	4067
rs764382367	snp	A/G			downstream-variant-500B	LYN	GRCh38.p7	8:56012806	TTTGGTTTGACCCAT[A/G]TTACAAAGCCCAGCC	4067
rs764429528	snp	A/C	5.09022e-05	0.00504465	intron-variant	LYN	GRCh38.p7	8:55952139	AAACTGAAGGTTCAA[A/C]AAGACAAGATATATT	4067
rs764447790	snp	C/T	8.2464e-05	0.00642069	synonymous-codon	LYN	GRCh38.p7	8:55953878	GAAGGCTTGTATTAG[C/T]CCCAAGCCACAGAAG	4067
rs764464934	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55948786	ATGACCTTGACAAGA[C/T]CCTTAAACTTTATAC	4067
rs764505424	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55932316	GCTACTAATTACTAG[C/T]GACAGATTAATATAG	4067
rs764520104	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55905031	AGTATTTTTTAGAGT[A/T]CCCCAGGTGATTCTG	4067
rs764521914	in-del	-/T			upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55879050	TACATCTTGGATTTG[-/T]TAAGTGGCATTTATT	4067
rs764543708	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55982879	CTGCAGCCGCTCCAG[A/C]CCCTACAGCCTCAGC	4067
rs764569894	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55955106	TTTAAACACTCTCCA[G/T]CCCCGGCAGAACAGA	4067
rs764572238	in-del	-/TGT			intron-variant	LYN	GRCh38.p7	8:55970908	CCTGCTTTAAGGAGA[-/TGT]TGTTGAGAGTCACAT	4067
rs764604690	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55999841	CCAGGCATGGTGACG[C/T]ATGCCTGTAATCCCA	4067
rs764630960	snp	A/G			utr-variant-3-prime	LYN	GRCh38.p7	8:56011227	CTAATAAGCCACGGT[A/G]GCAGGAGGTTCAAGC	4067
rs764635734	snp	A/G	1.64781e-05	0.00287033	synonymous-codon	LYN	GRCh38.p7	8:56010038	AGAAGAGAGACCAAC[A/G]TTTGACTACTTACAG	4067
rs764645431	snp	C/T	3.2956e-05	0.00405918	missense	LYN	GRCh38.p7	8:55950523	TTCATCCCCAGCAAC[C/T]ATGTGGCCAAACTCA	4067
rs764657002	snp	G/T			upstream-variant-2KB	LYN	GRCh38.p7	8:55877062	ATTAATACATAACCT[G/T]ATATGGTGTGTGTTT	4067
rs764719905	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55941296	CTGACTCCTGACCTT[C/G]CCTACCTGCTCCTTG	4067
rs764753003	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55981279	TCTCGGTCCCCGCCC[A/G]TTTCTTCCATAGCGT	4067
rs764807758	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55953580	TTGAACCCAGGAGGC[A/G]GAGGTTGCAGTGAGC	4067
rs764809837	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55928211	AAAGCAGTGGTGCAA[G/T]CTCAGCTCACTGCAA	4067
rs764816578	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55892745	AGTTCTTTCTAACAG[G/T]ATTCGAGGGAATTTT	4067
rs764840644	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55991125	CGGGGTCTGAGGTCT[A/C]TCCCTGATCCCACTC	4067
rs764844795	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55987228	GACCACACTGGGGAA[C/T]ATGATGAAACACCGT	4067
rs764893950	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55882290	CGCCCCTGCCCTCCA[A/G]TAGCTTTCTTTTAGC	4067
rs764897689	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55930068	GAGGGATCTAAGTTA[C/T]GTGCTCCTTGTGAAA	4067
rs764898944	snp	C/T	1.66308e-05	0.00288359	intron-variant	LYN	GRCh38.p7	8:55947770	GTTTCCTCAGGCCAC[C/T]GAGTCCTGCAGGCTG	4067
rs764907789	snp	C/G			downstream-variant-500B	LYN	GRCh38.p7	8:56012551	CAATATAGCAAGTCT[C/G]TACAAAAAATTTTAA	4067
rs764909166	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55893870	TTCACAGGCACGATT[A/G]TCACTCACACACTAT	4067
rs764933395	snp	A/G	3.29462e-05	0.00405857	missense	LYN	GRCh38.p7	8:55969741	TGGATTTCCTGAAGA[A/G]CGATGAAGGTGGCAA	4067
rs764942002	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55919155	AGAAAGAGGATCTCA[A/G]TTATTTCAAGAAAAG	4067
rs764954608	snp	A/C			intron-variant	LYN	GRCh38.p7	8:56007609	CATGTCTTCTTTCAG[A/C]GGTTTAAATTCAGGA	4067
rs765009798	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55970560	GTATGTAGCAAAAGA[A/G]ATTTATAGAAGTTCT	4067
rs765032784	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55942885	AATAGGTGCTAATGT[A/G]TCTTTTGTTGTATCA	4067
rs765033199	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55930322	ATTTCATAATAATTT[A/C]TATTATGTTACATGC	4067
rs765082667	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55888764	GTTTTTGAGACAGAG[A/T]CTCACTCTGTCATCC	4067
rs765083443	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55937650	CATTGCTAGATTTTA[C/T]GAAACCAAAACCCTA	4067
rs765089783	snp	C/T	1.6869e-05	0.00290417	intron-variant	LYN	GRCh38.p7	8:55998298	CTTGATGGCACTTTC[C/T]AGTCACCTACCCTAC	4067
rs765115811	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55908687	GCTTTTAGTGTAACC[A/G]TCATCTGAGTAGCAC	4067
rs765133444	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55898435	CTGAGACCACAGGCA[C/T]GTGCAACCATGCCTG	4067
rs765215577	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55949658	AAGTCAGCGTAATTA[A/G]CATATCCATCATCTG	4067
rs765240454	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55934778	AAACCCACTTCCCAC[C/T]TCACCCCCCTTTCCC	4067
rs765281574	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55988105	AAGAATGCATGAGCT[A/C]TCTGTTCCATCCCTT	4067
rs765297250	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55946389	ATCATATATACAACA[C/T]GAATGTGAGTAAGAA	4067
rs765300787	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55917267	TGTAGGTCACTGCAG[C/G]CTTGAACTCCTAGGC	4067
rs765309009	in-del	-/G			intron-variant	LYN	GRCh38.p7	8:55996383	ACCAGGGATACTGTT[-/G]GCAGATGACTGGGGA	4067
rs765324280	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55957556	AAAGCATCAAATTGC[A/G]TGCTATTTGCTCCTG	4067
rs765327417	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55975532	ATGCAGATGACATTG[A/T]TATAAGATTTTAGCA	4067
rs765363749	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55947327	TTATTTCCACATCTT[A/G]GCTATTTTGAATAAT	4067
rs765367815	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55995387	AGGGGACACGAAGTC[A/C]CTGCTCTCCAAACCT	4067
rs765381942	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55963700	GTGTTTATTACTCAT[A/G]TGAATTTCTTCTTTT	4067
rs765393472	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55985290	TTCTTCCTCAGCTTC[A/G]GCCCTTGCAGCCACA	4067
rs765437033	in-del	-/C			upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55879422	CGAGACCCCGAGCAT[-/C]CACCTCGGCATATCG	4067
rs765437658	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55946166	ATATTAGGGCTCTGT[C/T]ACCAAAGAAGAGGAG	4067
rs765452178	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55902197	ATTTTTAGTAGAGAC[A/G]GGGTTTCTACATGTT	4067
rs765478646	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55979834	CCCAAGGCTCAGAGG[A/G]ATGCCACAGCATCTC	4067
rs765511296	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55925379	TCCTCCCGCCTCACC[C/T]CTGAAAGTGCTGGGA	4067
rs765518184	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55913569	AGGGGTTGAGGAGAA[A/G]TAATTACACATAAAT	4067
rs765532833	in-del	-/TTC			intron-variant	LYN	GRCh38.p7	8:55971856	TAGAAATGAATAGGG[-/TTC]GGAGAAGCTACTTTC	4067
rs765580974	in-del	-/C			intron-variant	LYN	GRCh38.p7	8:55944861	CAAACCCACACACCG[-/C]CTTTTTCCTCTTGTT	4067
rs765585694	snp	A/G	1.66001e-05	0.00288094	intron-variant	LYN	GRCh38.p7	8:55954034	GAGATGGTGACAGGA[A/G]AAGTAAAGGCTCAAG	4067
rs765585716	snp	A/G	1.65641e-05	0.00287781	missense, intron-variant	LYN	GRCh38.p7	8:55941887	AAATCAAAAGGGAAA[A/G]ACAGCTTGAGTGACG	4067
rs765590021	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55982480	TATTTTTGATGCATT[A/G]CAAGGAGCTGTACGG	4067
rs765596924	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55964464	CCAAAAGAAACATCA[A/T]TGGATAGGTTGACTG	4067
rs765602172	snp	C/G	3.32912e-05	0.00407976	intron-variant	LYN	GRCh38.p7	8:55942019	TCTCAGGGGAGAATT[C/G]CCACAGCAAGATCAA	4067
rs765634274	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55886541	GCATGAGCCACGCGC[C/T]CAGCCTGTCAAACTT	4067
rs765648349	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55981215	ACCTTCCCTGACCTT[C/G]CTTCTGAAGCAGTTC	4067
rs765659812	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55941210	CACTGCAGATTGGAT[A/G]TGTCATTTGTCTTCA	4067
rs765716826	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55912551	GCCAACGTGGCGAAA[A/C]CCCGTAGCTACTAAA	4067
rs765754768	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55930121	CCCCCCACCTGACCC[C/T]GCTCTGTGGAAAAAT	4067
rs765759201	snp	C/G			utr-variant-3-prime	LYN	GRCh38.p7	8:56011558	AGGAGTTGATTGCCT[C/G]AACACCTGAACATCC	4067
rs765784983	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55885944	CATTTTCGGTTTGCC[C/G]TTAAGTGAGGGGTGG	4067
rs765799531	snp	C/T			intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55923997	GCCGCACAACTTCTC[C/T]AACCTTAGAATCATA	4067
rs765824423	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55985984	CCCGCCTGGGCAATA[C/T]AGTGAGACCTCATCT	4067
rs765838339	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55952594	AAAAGCAATTAATTA[A/G]TCTACAGTTAAATAC	4067
rs765894673	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55991777	TGCTCCCTTGTCCCT[A/G]TGCTCAGTAAACCGC	4067
rs765914538	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55929070	TTCAGTGTTGAATTG[C/T]CTTTGCTCTTTTTGA	4067
rs765937428	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55997014	AAAAATACAAAAATT[C/T]GCCAGGCATGGTGGT	4067
rs765942219	in-del	-/T			intron-variant	LYN	GRCh38.p7	8:55924373	TCATTTTTTTTTTTC[-/T]TTTTTTTGAGATGGA	4067
rs765987310	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55951262	AAAAAAAAAAGAGAA[A/G]AGAAAAGAAAAGTAC	4067
rs766052833	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55892660	TGATCCTCCCATCTC[C/G]AGATCCCAAAGTCCT	4067
rs766097079	snp	A/T			utr-variant-3-prime	LYN	GRCh38.p7	8:56010504	TGCAGAACTAAACTC[A/T]TTTATAAAGCTAAAA	4067
rs766104390	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55975184	GCATTGCTTGGAGCT[A/G]ATGCTTGGAAACCTC	4067
rs766111207	in-del	-/AG			intron-variant	LYN	GRCh38.p7	8:55906724	CCAAAAAAAAGAAAA[-/AG]AAAAAAAAAAGAGAG	4067
rs766146432	snp	C/T	1.691e-05	0.0029077	intron-variant	LYN	GRCh38.p7	8:55950410	ATTTTGATACATGCA[C/T]GGAGTATGTAATCTT	4067
rs766163425	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55901122	CTTGGGCACTTCGTG[A/G]CCGTGTGTCTCATAT	4067
rs766166625	snp	A/G	1.64781e-05	0.00287033	synonymous-codon	LYN	GRCh38.p7	8:55950552	CAACACCTTAGAAAC[A/G]GAAGAGTGAGTCCTC	4067
rs766215833	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55964790	AAAGAACAAGAGAAA[A/G]TAGAAGTCACTCCAA	4067
rs766292370	snp	C/T	3.295e-05	0.00405881	synonymous-codon	LYN	GRCh38.p7	8:55947673	CTATGATGGCATCCA[C/T]CCGGACGACTTGTCT	4067
rs766345275	in-del	-/A			intron-variant	LYN	GRCh38.p7	8:55905418	CCGTCTCAAAAAAAA[-/A]GAAAGAAAGAAAGAA	4067
rs766355605	snp	A/G	5.03132e-05	0.00501538	intron-variant	LYN	GRCh38.p7	8:55998314	AGTCACCTACCCTAC[A/G]TATGAAAATGGGAGC	4067
rs766357723	in-del	-/T	3.29701e-05	0.00406005	intron-variant	LYN	GRCh38.p7	8:55947613	TCTCTTGTGTTCATC[-/T]TTAGATCCAGAGGAA	4067
rs766360546	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55935062	GGTCATAGCCTAGAG[A/G]TGACGCCCACACCAT	4067
rs766382717	snp	C/T			upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55878543	TCTAGGCAATAGGCC[C/T]TCAGGTAGTGAATTA	4067
rs766424925	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55882182	TGTGGGGTGGTTAAG[A/T]TGTTTCCTGCAAAGG	4067
rs766432274	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55880765	CCGGCTGAGAGGAAG[C/G]GAGAGTTATTTTAAG	4067
rs766440641	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55945836	TCAGCCTCCAGGGAC[A/G]GAGCCCTGACCATGC	4067
rs766444614	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55983079	CCTCATGTCCACACA[A/G]CAGCTGTGACCTGCA	4067
rs766456199	snp	A/C			intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55923847	CCCGGCCAAGATCAA[A/C]CAACTTAATAAATGT	4067
rs766468483	snp	A/G			upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55877897	GAACTATTTTAAAGC[A/G]CCCAACATAATTTCT	4067
rs766491825	in-del	-/T			intron-variant	LYN	GRCh38.p7	8:55973630	GAGAGGAAAGAGCAG[-/T]TGAAAAATTTACAGT	4067
rs766498334	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55905103	ATGTGGGAATCTTTC[A/G]GCTATTTTAGAAAAC	4067
rs766524817	snp	C/G			upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55878694	CATGGGCAACCCACC[C/G]CTTCTCTTCAGCAGT	4067
rs766549742	snp	G/T	1.6495e-05	0.0028718	intron-variant	LYN	GRCh38.p7	8:55951955	ATTTACTTACACTTT[G/T]CCCCCCATAGGAAGC	4067
rs766575297	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55956201	GGCAGGAATAGTATA[A/G]TGAATATTGTATACC	4067
rs766575309	in-del	-/CA			intron-variant	LYN	GRCh38.p7	8:55987406	AGTGAGACTTCATCT[-/CA]AAAAAAAAAAAAAAA	4067
rs766598941	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55889776	AGAGCACAGGGTGTC[A/G]AATTAATTTCATGTG	4067
rs766599562	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55911909	TGTGATATGGACAGG[A/T]CTTATTGATGGGGTG	4067
rs766623489	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55901939	TGACTGCACAGACAC[A/G]GGAAAGGATCTGGTT	4067
rs766636491	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55946301	ATGCACCTCTACAGG[C/T]TTTTCCCTCTGTGCT	4067
rs766698807	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55916279	AAAAAATAGTGACTG[C/T]GTTCAATGTTACGCT	4067
rs766710298	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55885793	ATGCTGGAGAGAAAA[C/G]GCCCCAGAGGAGGCA	4067
rs766757650	snp	A/C/G/T	8.42591e-05	0.00649029	intron-variant	LYN	GRCh38.p7	8:55946522	GCAACATAGTTAAAA[A/C/G/T]TTTTTTTCTTTACTA	4067
rs766830755	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55963620	ATTTTTGCTGAGCTC[A/G]GCAGTGGTTTCTCAT	4067
rs766869389	snp	C/T	1.648e-05	0.0028705	synonymous-codon	LYN	GRCh38.p7	8:55999530	CGAAATTGTCACCTA[C/T]GGGAAAATTCCCTAC	4067
rs766869647	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55950953	AGTTGTGCTACTAAA[A/G]GTAATATAGTTGAGT	4067
rs766878182	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55884924	AGCATTCCTTATTTG[C/T]CACAGAGCTATTTCT	4067
rs766889035	in-del	-/TGT			intron-variant	LYN	GRCh38.p7	8:55962403	CTTCAGTCCCTATGA[-/TGT]TGGTGAGATGCATCC	4067
rs766894914	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55939887	GTATTAAAAAATGTG[C/T]TGTTTTGAATCAAAG	4067
rs766917926	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55934656	TTCCTCAGTGCTCAA[C/T]CCTGCATGAGACATG	4067
rs766929047	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55896069	CTTTTATCATTAGCT[C/T]ATCCTTAAGCATCTC	4067
rs766938216	snp	C/T	6.73786e-05	0.00580386	intron-variant	LYN	GRCh38.p7	8:55946523	CAACATAGTTAAAAT[C/T]TTTTTTCTTTACTAT	4067
rs766946163	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55951895	TATCACAAAATGTGT[A/G]CTGCAGTTGTTGTAT	4067
rs766947795	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55943596	AAAAAAAAAAAAAAG[A/G]CATTTTTATAGTTTC	4067
rs766950099	snp	G/T			intron-variant	LYN	GRCh38.p7	8:56008537	ATAGATACTGCTAGA[G/T]GAGCACATAATTGAA	4067
rs766955887	snp	G/T	3.29652e-05	0.00405974	missense	LYN	GRCh38.p7	8:55966831	CAGCATGACAAGCTC[G/T]TGAGGCTCTACGCTG	4067
rs766966965	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55928068	CTCTGCCTCTTTGCC[A/C]GCATTTGGTGTAGTC	4067
rs766979210	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55978325	GAGGATGGGCCTGAG[A/C]GAGGTCAGTGTTGCC	4067
rs767032651	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55979609	GCCCCCATTTAAGAC[C/T]GGTTTGACTGAAATG	4067
rs767063583	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55962556	ATGCATCTGTGGCTA[C/T]GGTTCATTCATCTTC	4067
rs767073652	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55900875	AACTCTTTATCTTAA[A/C]ATGCTGCCACAAAAT	4067
rs767149526	snp	A/C	1.64765e-05	0.00287019	intron-variant	LYN	GRCh38.p7	8:55969701	ATGCACTAACTTGTT[A/C]TTTCTTTCTCCATAG	4067
rs767209881	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55910991	AACCTCCGCTTCCCG[A/G]GTTCAAGCGATTCTC	4067
rs767213766	snp	C/T	0.000132055	0.00812465	synonymous-codon	LYN	GRCh38.p7	8:55950711	TATAACCAGGAAGGA[C/T]GCAGAAAGGCAGCTT	4067
rs767214391	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55990493	TGGAAAGGGAATGGG[A/G]TTCTCTATAGAATAT	4067
rs767225980	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55985299	AGCTTCGGCCCTTGC[A/C]GCCACACCCACCTGC	4067
rs767236042	snp	C/T			intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55923179	TTGTCTGTCATACTA[C/T]TTAAGTAATTTAAAA	4067
rs767252080	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55947361	GCTGTGAACATGGGT[A/G]TATAATTTCTTAAAT	4067
rs767256573	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55977481	TTTGACTTTTGGAGA[A/G]TCACAGAGTTCTCAG	4067
rs767265901	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55899601	TCAACCAATCCTTAT[A/G]ACAAGTGTGTGAAGT	4067
rs767272581	in-del	C/GTGTCTTTTT			intron-variant	LYN	GRCh38.p7	8:55909989	TGTGTGTGTGTGTGT[C/GTGTCTTTTT]TTTTTTTTTTTTGAG	4067
rs767304702	in-del	-/T			intron-variant	LYN	GRCh38.p7	8:55910900	TTTTTACTAATTTTG[-/T]TTTTTTTTTTTTTTG	4067
rs767314827	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55993186	TTTAATTCAGTAATT[A/C]TTCCTGGAGGAATAA	4067
rs767319385	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55910544	ATGCTGTTTTGGTGA[C/T]TATATCCTTGCAGAA	4067
rs767328143	snp	C/T			upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55879094	GCTTGAGCACGCGGT[C/T]ACACATTCTTTCAGC	4067
rs767376738	in-del	-/T	6.67858e-05	0.00577827	intron-variant	LYN	GRCh38.p7	8:55946418	AAAAGCTAAACAGAA[-/T]TTTTTTTTCTAACAA	4067
rs767377597	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55891682	ACTTAAAATAGTTAC[A/G]ATACAAGTTTTATAT	4067
rs767395599	snp	A/G	1.64754e-05	0.00287009	synonymous-codon	LYN	GRCh38.p7	8:55999467	AGCAATCAACTTTGG[A/G]TGTTTCACTATTAAG	4067
rs767403182	snp	A/G			utr-variant-3-prime	LYN	GRCh38.p7	8:56010386	GCAGCCGTTTGAGAA[A/G]AAAACATCTATTCTC	4067
rs767417800	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55969340	TGAATACAGATGGGA[A/G]TGAGCCTGGCCAAGT	4067
rs767424248	in-del	-/ATTTGGCTTA			intron-variant	LYN	GRCh38.p7	8:55884417	GCCTTTCTGGGGTAT[-/ATTTGGCTTA]AGTTAGTTGGAAGGG	4067
rs767437628	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55946295	GGCAGGATGCACCTC[C/T]ACAGGTTTTTCCCTC	4067
rs767490331	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55928868	CAAGGTCATCTAGCT[C/T]TTCTCCTATGTTATC	4067
rs767490599	snp	G/T	4.94425e-05	0.0049718	intron-variant	LYN	GRCh38.p7	8:55950587	GTTGTCATCTTGGTG[G/T]CTTTATTTGCCACAT	4067
rs767549744	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55956004	CAAATTATTATGTGG[A/T]CACATTTTCATTTCT	4067
rs767562213	snp	C/T			utr-variant-3-prime	LYN	GRCh38.p7	8:56010249	TAGAGGCTAAATTAC[C/T]CAGGAAGAACACCCT	4067
rs767579206	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55914807	TCTCTTCACTCCCAC[A/C]CCTCCTGTTCATTTT	4067
rs767602180	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55888517	CCAAGAGCGAAGACA[C/T]GTTGAACACTGACTT	4067
rs767602728	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55955311	AAGTCTTTCTGCACA[C/T]ATTTGCAGAATTCAG	4067
rs767606134	snp	C/T			intron-variant	LYN	GRCh38.p7	8:56001757	GTCAGATTATGTATA[C/T]AATCTGACACCTGAT	4067
rs767630196	snp	A/G	1.65031e-05	0.00287251	synonymous-codon	LYN	GRCh38.p7	8:55953860	CTTGTGCAGAAGATT[A/G]GAGAAGGCTTGTATT	4067
rs767648593	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55981999	AGGTTTGTCCTCCCC[C/T]AGTGTCATGCAGGGC	4067
rs767653285	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55898395	CCGTGTTCAAGCAAT[C/T]CTCCCATCTCAGCCT	4067
rs767680075	snp	A/G	1.65608e-05	0.00287752	missense	LYN	GRCh38.p7	8:55952097	CCCTGTATCAGCGAC[A/G]TGATTAAACATTACC	4067
rs767696028	snp	A/G			upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55879173	CTGGGACGCAGCTGT[A/G]GTAGGAATGAAATAA	4067
rs767713659	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55954079	CTTCTGAGCCAGACA[A/C]TAAATTATGTCAGAA	4067
rs767713799	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55978952	TTCTCCTCTGCTGCC[A/G]CTTTTCTCTCCATGC	4067
rs767717546	snp	A/G	1.66946e-05	0.00288912	intron-variant	LYN	GRCh38.p7	8:55941829	TGGAATGGTAAAACA[A/G]TGTCATTACTTTTAT	4067
rs767721952	in-del	-/A			intron-variant	LYN	GRCh38.p7	8:55995886	CTTTGAGACTGATGT[-/A]AGGCCACACTGATTA	4067
rs767723020	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55921909	CAAGTGCCGAACAAT[A/G]TTTCTTGCACTGATA	4067
rs767725251	snp	A/T			intron-variant	LYN	GRCh38.p7	8:56006094	GTCTCAAAAAAAAGG[A/T]GGGGGTGTCTTGTTG	4067
rs767762873	snp	A/G			upstream-variant-2KB	LYN	GRCh38.p7	8:55877214	TTAGCAACAACAGAC[A/G]GCACTTTAGCAAGCT	4067
rs767770076	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55966208	ATAGAAACCTTTTGA[A/T]TTTTGAATAATTTAA	4067
rs767778419	snp	G/T			intron-variant	LYN	GRCh38.p7	8:56007489	TCAGAATTAGACTCA[G/T]GAAAATGGATTTGCT	4067
rs767796440	snp	A/G	4.94303e-05	0.00497119	missense	LYN	GRCh38.p7	8:56010013	TGAAAATGTGCTGGA[A/G]AGAAAAGGCAGAAGA	4067
rs767804351	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55887136	TTACAGTTACTAATA[C/T]GAAAAATTTTTTTTC	4067
rs767841274	snp	A/T			intron-variant	LYN	GRCh38.p7	8:56004518	AGGCTGGTCTTGAAC[A/T]CCTGACCTCAGGTGA	4067
rs767845042	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55926481	TAAATGGCTATGGGC[A/G]TATTAGGAGTGATGA	4067
rs767857994	snp	A/G	1.6617e-05	0.00288239	synonymous-codon	LYN	GRCh38.p7	8:56009909	TTTTTCCACCCTAGG[A/G]AGAACTAATGCCGAC	4067
rs767865117	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55940687	CTGTTTTGTTTTTAA[C/T]GCATAGATTTGACCC	4067
rs767868867	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55988792	TTAGCTTTGCTTGAG[A/C]GATCACATTCAGCCC	4067
rs767874105	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55934544	CCCACCGTGCAAGTG[C/G]ATGCAACTGGGAAAC	4067
rs767892875	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55904762	TCAAAAAAGAAAAAA[A/G]AGAAGATAAACATAA	4067
rs767899958	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55925663	AGGAAGCAGGCCGCC[C/T]GTGACACCAAGGCAT	4067
rs767927179	snp	C/T			intron-variant	LYN	GRCh38.p7	8:56002055	GGAGGCTGAGGCAGG[C/T]GGATCACCTGAGGTC	4067
rs767938686	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55895913	TACCCACTCCCTACT[C/T]ATGGTACCCCTGGCC	4067
rs767953650	snp	C/T	3.29864e-05	0.00406105	intron-variant	LYN	GRCh38.p7	8:55951960	CTTACACTTTTCCCC[C/T]CATAGGAAGCTTCTC	4067
rs767967859	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55961275	AAAGTGTCACTCCAC[A/T]AGACGCTTTTTACTA	4067
rs767967877	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55972174	ATGAACTGCTCAGTG[A/T]CACTGGGAGAGTCAC	4067
rs767974744	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55983035	TAAAATGCCAGCCCT[A/G]TGGAAGTCCGACCCT	4067
rs767991472	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55895286	ACTGACCAGAGCAGA[A/G]CAGTTTCCAAGTGAA	4067
rs768019017	snp	C/G	1.64746e-05	0.00287002	missense	LYN	GRCh38.p7	8:55947662	GCCTTGTACCCCTAT[C/G]ATGGCATCCACCCGG	4067
rs768020877	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55962420	TTGGTGAGATGCATC[C/T]GTGCTTTTGGGTGTG	4067
rs768036059	snp	C/T	1.64768e-05	0.00287021	intron-variant	LYN	GRCh38.p7	8:55969828	CCGTGTGCACGTGCA[C/T]TTGCAAAGACTTCCC	4067
rs768110333	snp	A/C			intron-variant	LYN	GRCh38.p7	8:56001899	CAAAGCTGCTCTGAG[A/C]CCCAGATCCATGTGC	4067
rs768141605	snp	C/T			utr-variant-5-prime	LYN	GRCh38.p7	8:55877727	TCTTGCCCCGCCCAT[C/T]GTATTCCTTCCTTTC	4067
rs768150562	snp	A/C	0.000171512	0.00925886	intron-variant	LYN	GRCh38.p7	8:55880116	CGGGTGAGTCCTCTG[A/C]GCGAGCCCAGGGGTG	4067
rs768172058	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55907929	AAAATGTATATCTAA[A/G]TAAGAGACAGGGCTT	4067
rs768181879	in-del	-/AAGTC			intron-variant	LYN	GRCh38.p7	8:55991945	AGCACATCTCAGCTT[-/AAGTC]AAGAGTATGGAAACC	4067
rs768187415	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55934414	AGGTACAGGGTTGCT[A/G]CTGTGCTGTTTGGTA	4067
rs768200823	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55971496	GAGGAGTGTAACAAA[G/T]GTTTGTCACACTTGT	4067
rs768212088	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55916703	CTCTGGCTCCATACT[A/G]GAAATGTGTGTGGCA	4067
rs768213433	snp	C/T	1.64817e-05	0.00287064	synonymous-codon	LYN	GRCh38.p7	8:55998414	GCGAGCAGCTAATGT[C/T]CTGGTCTCCGAGTCA	4067
rs768233887	in-del	-/T	1.85115e-05	0.00304227	intron-variant	LYN	GRCh38.p7	8:55966678	CGGCTAGATTTTCTG[-/T]TTTATAAAGCATGCC	4067
rs768238641	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55945569	TTAATCAAAGAGAGA[C/G]AGAAAAGTTACATGA	4067
rs768264070	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55972980	TTGAATGTTCACAAG[C/G]GGTGGTTAAATTCAG	4067
rs768269573	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55905660	GGAGTCCTTTCTTTT[C/T]CTAGTCACCCCCAAA	4067
rs768320788	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55904675	GAATTGCTTGAGCCC[A/G]GGAGGTGGAGTTTGC	4067
rs768344974	snp	C/T	1.69513e-05	0.00291125	intron-variant	LYN	GRCh38.p7	8:55953807	TATTGCATTTCTTAA[C/T]CTTCATTTTTCCCTT	4067
rs768355993	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55983578	CTCGACCCCAGCAGC[A/G]CAAGTCAGCAGTGAC	4067
rs768384321	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55941042	TCTTCTCTCCCATAA[A/G]TGTGTTTCCTCAATT	4067
rs768386970	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55958874	TTGATGGACAATTAG[A/G]TTGTTTCTACCTTTT	4067
rs768390609	in-del	-/AG	1.66247e-05	0.00288307	intron-variant	LYN	GRCh38.p7	8:55942008	TAAGTAGATAGTCTC[-/AG]GGGAGAATTCCCACA	4067
rs768402167	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55901815	CTGAGTCATTATCAA[A/G]TTGCATTTCCTGGCT	4067
rs768430654	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55886342	CCTCCCAGGTTCAAG[C/T]GATTCTGCTGCCTCA	4067
rs768499390	snp	A/G			utr-variant-3-prime	LYN	GRCh38.p7	8:56011049	TTCAAATATTTGAAC[A/G]TTATGTTAAAGATCA	4067
rs768523865	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55980422	TTGATTCCGAACTTA[G/T]TGCAGACACCGGATG	4067
rs768561923	snp	A/G	1.65244e-05	0.00287436	synonymous-codon	LYN	GRCh38.p7	8:56010104	GCAATACCAGCAGCA[A/G]CCTTAGAGCACAGGG	4067
rs768602557	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55969072	GATTGCTTGAGTCCA[A/G]GAATTTGAGACCAGC	4067
rs768631968	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55951431	AATGCTTTGGGAGGC[C/T]GAGACTGAGAATCAC	4067
rs768642915	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55885449	GACACCAGACCATAC[G/T]GGTTGGAAGCTTCTT	4067
rs768647096	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55976704	GCAGGTGGAAGGTGG[A/G]CTTCCTGGAGGAGGT	4067
rs768670317	snp	C/T	1.64808e-05	0.00287057	synonymous-codon	LYN	GRCh38.p7	8:56009975	CCGTGTGGAGAACTG[C/T]CCAGATGAGCTCTAT	4067
rs768690000	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55909849	TTAATTTGCATTTTT[C/T]TGATGATTGGTGTTA	4067
rs768711450	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55942823	TAGTGAGATTAGCTC[A/C]GTGGTTTAGAAGCAA	4067
rs768766081	snp	A/G			intron-variant	LYN	GRCh38.p7	8:56007043	CGAGAGTCCTTCAGA[A/G]CTAGGAGAACATACT	4067
rs768806997	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55937536	ATGCTAGCGGGAACA[A/T]CCTTATGCCCCTGTG	4067
rs768819807	snp	A/T	3.30376e-05	0.0040642	intron-variant	LYN	GRCh38.p7	8:55954004	GTGTGCGGCTCGGGG[A/T]TCTATGTCCTTCTAG	4067
rs768840421	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55921121	CGAAAACAATTTTGG[A/G]AGTTAACATTTATTA	4067
rs768869403	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55960620	ATTTTGAGCTGCTAG[A/T]ATTTAGTTTTCTCTT	4067
rs768873695	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55882956	GTCCCAATAAACCCA[A/G]TCGTAAGTTGAAAAT	4067
rs768877810	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55990753	GGAGAAGGGCATAAT[C/G]AGTCATGTCCAATTC	4067
rs768895514	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55920436	TTGTTTTGGAGGACG[A/G]GGGCGGATAATGGGA	4067
rs768923094	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55996054	TTGGTGACAAGTTTG[A/G]AGGCTCCAATGTATA	4067
rs768924996	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55888980	ATAGATGCCCAATGT[A/G]TGTAACAAAAATTTT	4067
rs768926566	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55894709	AGCTAATTTTTTTGT[A/C]TTTTTAGTAGAGACG	4067
rs768973187	snp	A/G			utr-variant-5-prime	LYN	GRCh38.p7	8:55877328	GTCTTGAACTCCTGA[A/G]CTCGAGCAATCCTCC	4067
rs768990818	snp	A/G	6.60001e-05	0.00574419	intron-variant	LYN	GRCh38.p7	8:55999383	TTTGTTTAAGTTTAA[A/G]TACCCAAGTAAGAAC	4067
rs769010583	in-del	-/A			intron-variant	LYN	GRCh38.p7	8:55951665	GCAACAACCTATTTC[-/A]AAAAAAAAAAAAAGA	4067
rs769016300	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55955742	TCTATGAATTTAACC[A/G]CTCTAGGTACCTCAT	4067
rs769045264	in-del	-/TTG			intron-variant	LYN	GRCh38.p7	8:55967330	TTTTTTTTTTTTTTT[-/TTG]GAAACAGAGTCTCAC	4067
rs769060155	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55899146	TTTTACTTTTGTATC[A/C]GGCAATAATTACCTT	4067
rs769066575	snp	A/G			intron-variant	LYN	GRCh38.p7	8:56000589	AAAAATTAGCTGGGC[A/G]TAGTGGTGGGCATCT	4067
rs769076571	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55953283	GGTTGTCTGTTGGCT[A/T]TGTTGTTTTTGTTCA	4067
rs769120131	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55929252	GGGATCCGTAGAATA[C/G]ATCCTTCTTACTGTT	4067
rs769138114	snp	C/G			upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55878534	TAAGAAAAGTCTAGG[C/G]AATAGGCCCTCAGGT	4067
rs769192442	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55927326	TCCAGAGTGTCATAC[A/G]GTTGGAATCACACAG	4067
rs769193489	snp	G/T			utr-variant-5-prime	LYN	GRCh38.p7	8:55877706	CGTATTTACAATACC[G/T]CCTTCTCTTGCCCCG	4067
rs769266207	snp	C/T			intron-variant	LYN	GRCh38.p7	8:56007974	AAATACAAAAATTAG[C/T]CGGGCATGGTAGTGG	4067
rs769283820	snp	A/G	3.29679e-05	0.00405991	intron-variant	LYN	GRCh38.p7	8:55999402	CCAAGTAAGAACCAC[A/G]TATCTTCTTCCTTAG	4067
rs769283825	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55956662	GCCGTCACTTCTCTA[C/T]AAAGCTCCAGTCCTT	4067
rs769284954	snp	C/T			utr-variant-5-prime	LYN	GRCh38.p7	8:55877506	GGCAGAGCATCGCCT[C/T]GTTCCACTATAGCTG	4067
rs769299070	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55903802	GAGGATTACTTGAGC[C/T]CAGGAGTTTGACACC	4067
rs769322434	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55938337	AACCAAATTCTCTAC[A/G]CATAAAATATGTCTT	4067
rs769357994	snp	C/T	1.65012e-05	0.00287234	intron-variant	LYN	GRCh38.p7	8:55950648	TCTTGCCGTGGAACA[C/T]AATATGCAGGAAATG	4067
rs769375491	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55945298	AAAATGATGTAATTA[A/G]TTTCTAGTCTTCTAG	4067
rs769376347	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55971988	CTGATGGGGCTGAGC[C/T]CCCTCGGTGACAGGA	4067
rs769413339	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55904568	TTCTGTATGTGTTAC[C/T]CTGCAGATCATGCAC	4067
rs769414598	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55915546	CCCGTCTCTACTAAA[A/G]ATACAAAAAATTAGC	4067
rs769428114	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55938573	AGTTACAGCAGACCT[A/G]TTCCCTACAATGTTA	4067
rs769571199	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55962907	TGAGCATGTCACACA[G/T]TGAGAGCAAGAGAGT	4067
rs769571925	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55900969	ATTGGCAAAGAAGAC[A/G]TGGATTGAGTGAGCC	4067
rs769656457	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55991257	TCCTGTTTCACACCA[A/G]CAGTGGGGGAGAAAG	4067
rs769661010	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55962071	TTTTACGTCTTGCCT[C/G]TTTTACTCAACGGGT	4067
rs769676636	snp	A/C	0.000189394	0.00972939	intron-variant	LYN	GRCh38.p7	8:55880136	GCCCAGGGGTGGGCG[A/C]GGGCACGCGGGCAGT	4067
rs769717154	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55948641	ATTAAATGTCACTGT[A/G]ACCTGCCAAATAGGG	4067
rs769734882	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55977991	GGACAGGACTTCTTC[C/T]GAGCTTTTTCAATTC	4067
rs769769478	snp	C/T	4.9643e-05	0.00498187	intron-variant, missense	LYN	GRCh38.p7	8:55941932	AAGACTCAACCAGTA[C/T]GTAATACTGAAAGAA	4067
rs769802335	snp	A/G	1.65348e-05	0.00287526	missense	LYN	GRCh38.p7	8:55953841	AATTAGAGCAGGCAG[A/G]TGGCTTGTGCAGAAG	4067
rs769806486	in-del	-/TA			intron-variant	LYN	GRCh38.p7	8:55942265	GTGCAAAGACCCCAC[-/TA]TATATATATATACAC	4067
rs769832033	snp	C/T	1.64849e-05	0.00287092	intron-variant	LYN	GRCh38.p7	8:55947613	TCTCTTGTGTTCATC[C/T]TTAGATCCAGAGGAA	4067
rs769881588	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55986308	CAGCAGTGTGTGAGA[G/T]TTCCAGTTTCTCCAC	4067
rs769884002	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55934224	GAGCGAGATCCGTCT[C/T]AAAAAAAAAGAAGGA	4067
rs769916307	snp	C/G	3.30611e-05	0.00406565	intron-variant	LYN	GRCh38.p7	8:55947735	AGGAGTAAGTGCTCT[C/G]AAGCACGCCACGGCT	4067
rs769925907	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55892315	GTCCCAGCTACTTGG[A/G]AGGCTGAGGCAGGAG	4067
rs769928913	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55906968	ACTGACCAAATGCTG[A/G]CAAGGATCAGGGAGA	4067
rs769952180	snp	C/T	6.66234e-05	0.00577124	synonymous-codon	LYN	GRCh38.p7	8:55946471	ATCTCAGCTTTTACC[C/T]GGACAGAGGTTTCAA	4067
rs769966259	in-del	-/TACGA			intron-variant	LYN	GRCh38.p7	8:55891679	TATACTTAAAATAGT[-/TACGA]TACAAGTTTTATATT	4067
rs769966767	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55880436	TCCCGGTGAGGGCCC[A/G]AGGGCCGGCTGCTGT	4067
rs769973090	snp	C/T			utr-variant-3-prime, downstream-variant-500B	LYN	GRCh38.p7	8:56012026	TATTAAATTTATCTT[C/T]GCCTTGTTTTGCTTC	4067
rs769988978	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55930695	GAGTTATGCAAATGG[A/G]GATGCGGCACGTGGT	4067
rs769989084	in-del	-/T			intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55924066	TTTTCTTTTTCTTTC[-/T]TTTTTTTTTTTATTA	4067
rs770000610	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55958982	TAAATCCAGAAGTGG[A/T]ATGGCTGGATCCTGT	4067
rs770005199	snp	C/T	1.73228e-05	0.00294297	intron-variant	LYN	GRCh38.p7	8:55966939	TGCAAGGGCTTCAAA[C/T]TCAAAAAGTAAAATG	4067
rs770035711	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55918476	CAGGATTAAGAATCA[C/T]TGCCTTCTGCATCAA	4067
rs770036116	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55930021	TAGTAGATTCTCATA[A/G]GGGCGTGAACCCCAT	4067
rs770042280	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55987703	TTATAGGCATGAGCC[A/T]CCATGGCTGGCTCAA	4067
rs770077634	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55926093	CACTTTCAAGGTGAT[G/T]CTTGCACATAATTTA	4067
rs770078913	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55953045	TCCCAAAACACGGAG[A/C]GAGCAACGTGCTTCC	4067
rs770081038	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55970004	TTGAGTTTTGACCTG[C/G]ATATCATCTTCTATA	4067
rs770091060	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55972737	TTATTATTAAAGCTG[C/T]CCCACGGTGACAGAG	4067
rs770115531	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55997692	AACATTCAGACCATA[A/G]CATCTGTTTTCTGAT	4067
rs770159589	snp	A/G	1.66438e-05	0.00288472	intron-variant	LYN	GRCh38.p7	8:55950787	GAAACATTAAAAGGT[A/G]GGAAATTGTTCAAAG	4067
rs770161458	snp	C/T	4.94425e-05	0.0049718	synonymous-codon	LYN	GRCh38.p7	8:55966813	AACCTCATGAAGACC[C/T]TGCAGCATGACAAGC	4067
rs770180571	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55965380	GTGGGGGAGGAGTGG[A/G]GGGAGTGGCTCCCTG	4067
rs770201598	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55958006	CTGGCATCAAAAGTG[C/G]TGCTGTCAGCTGTGG	4067
rs770218432	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55974938	TAACCAGGAGGCCAG[A/T]TCCGCTCCCCACTCC	4067
rs770225444	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55907954	GGGCTTAATTACTAT[C/T]GCAAACATTTTATTA	4067
rs770254862	in-del	-/TTT			intron-variant	LYN	GRCh38.p7	8:55900540	ACCATGCCCAGCTAA[-/TTT]TTTTTTTTTTTTTTT	4067
rs770273905	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55925081	GCTTGCTTCAGCCTT[C/T]CAAAGTGTTGGGATT	4067
rs770322058	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55937295	ATGGATTGTGTACAT[A/G]TATTAGGTTGGTGCA	4067
rs770341350	in-del	-/AAT			intron-variant	LYN	GRCh38.p7	8:55993349	TTTGTACTTAACAAC[-/AAT]GAGAGGAAACCTCAG	4067
rs770344717	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55887947	AGGATATAAGGAGCA[A/G]TGGAATGAAGCCAGT	4067
rs770363007	in-del	-/TG			intron-variant	LYN	GRCh38.p7	8:55909976	TAATGGGGTTGTTTG[-/TG]TGTGTGTGTGTGTGT	4067
rs770377718	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55970701	TGCATGAGTACAGAG[A/G]TGAAGCACCTCACCT	4067
rs770400542	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55980967	CCCCTGGCCACCCCC[A/G]TGCTGTTCTCGGTCT	4067
rs770410618	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55977779	AAAAAAATTAGCCAG[G/T]CCTGATGGTCGTGCC	4067
rs770422370	in-del	-/C	1.67399e-05	0.00289304	intron-variant	LYN	GRCh38.p7	8:55953818	TTAACCTTCATTTTT[-/C]CCTTTCAAATTAGAG	4067
rs770427238	snp	A/C			utr-variant-5-prime	LYN	GRCh38.p7	8:55877386	TACAGGCATGAGCCA[A/C]TGAGCTCAGTCGCTT	4067
rs770433759	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55965271	GGCTACTTGAACAAG[A/T]GTTCTGAGGTCAAGA	4067
rs770444675	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55993043	CAAAAATTGATCCCT[C/T]AGGGGTGATAAAAAT	4067
rs770459006	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55953387	GCTTGGTGGCTCACA[C/T]CTGTAATCCAGCATT	4067
rs770463914	snp	C/T			upstream-variant-2KB	LYN	GRCh38.p7	8:55876744	CCCACACAGTGGCAG[C/T]GGGATGGGTTGCAGC	4067
rs770493032	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55898159	TTTCTTGTGCCACCC[C/T]CAGCCCAATGCCTGG	4067
rs770520912	snp	C/T	1.65034e-05	0.00287253	missense	LYN	GRCh38.p7	8:55950685	TGTCTTCACAGGTGG[C/T]TTTTCAAGGATATAA	4067
rs770531537	snp	A/G	4.96151e-05	0.00498047	intron-variant	LYN	GRCh38.p7	8:55999596	TGTATAAATGAGAAA[A/G]AGTCAGGTTGCATGA	4067
rs770538612	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55914395	TAGGGTGCAAATGCT[C/G]CCCTAAAGTGAGAGT	4067
rs770568875	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55921266	AATTCAACAACTGGT[A/G]CTTTGTTGCTGACTT	4067
rs770569459	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55954502	AGATTATAGCAGTGG[C/T]TTTTTCCAGGGGATT	4067
rs770590931	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55949608	CATGGGATACAGAGC[A/G]ATATTTTGATACATG	4067
rs770592533	in-del	-/ATATATATATATACACACACACACACAC			intron-variant	LYN	GRCh38.p7	8:55908998	TGTATGTATATATAT[-/ATATATATATATACACACACACACACAC]ATATATATATATACA	4067
rs770618069	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55886505	TGCCTGCCTCGGCCT[A/C]CCAAAGTGCTGGGAT	4067
rs770621553	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55960784	CCATTTCATTTTATG[C/G]TCTGCATTTTTTTGG	4067
rs770716598	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55918565	CTAGAAACGATTGTT[A/G]AGGAATAATAATGCA	4067
rs770738990	snp	C/T	6.65425e-05	0.00576774	intron-variant	LYN	GRCh38.p7	8:55946443	TAACAAATATTCTCT[C/T]GTAGGTTCCAGAATC	4067
rs770763726	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55953388	CTTGGTGGCTCACAC[C/T]TGTAATCCAGCATTT	4067
rs770788926	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55971042	TTCCAGTAAAGGTGT[A/G]TGATGGGTGAGTCAC	4067
rs770829276	in-del	-/TG			intron-variant	LYN	GRCh38.p7	8:55968670	TAAGTACTATTGTTC[-/TG]TGTCATAGATGAGAT	4067
rs770850614	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55929820	TGTTGTAGAGAAGCA[G/T]ATTTATTTATATCCA	4067
rs770864186	snp	C/T			intron-variant	LYN	GRCh38.p7	8:56001619	ACTGAGATTAATGAA[C/T]TAACATTGCTGCAAA	4067
rs770873268	snp	A/G			utr-variant-3-prime	LYN	GRCh38.p7	8:56010958	TTGTTTTGACAATGT[A/G]GTTTGGAAGAACTAA	4067
rs770877082	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55957907	GAGCTGAGATTGCGC[C/T]GCTGTCACCAAACTG	4067
rs770881227	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55926895	CTGCTCCTTGTGGAG[C/T]CCGGCTAACTCCTAG	4067
rs770883986	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55920483	CTTGCTCTGAGAGAG[C/T]ATTTAACATATGCTA	4067
rs770928751	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55962714	CCATTTACTGATGAA[A/G]TTGGAGTTCATGTTA	4067
rs770932618	snp	A/C	1.65913e-05	0.00288017	utr-variant-3-prime	LYN	GRCh38.p7	8:56010129	ACAGGGAGACCCGTC[A/C]ATTTGGCAGGGGTGG	4067
rs770938960	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55931581	ATTTCTTTTCAGACT[G/T]TTTTCTATTCATTTG	4067
rs770953840	snp	C/T	3.30956e-05	0.00406776	intron-variant, missense	LYN	GRCh38.p7	8:55941948	GTAATACTGAAAGAA[C/T]TATTTATGTGAGAGA	4067
rs770958749	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55996480	TGTGTGAAAAATTCG[A/G]ATCAGAGTTTTCTCT	4067
rs770978844	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55903090	CTGACTTCGCGATCC[A/G]CCCACTTCAGCCTCC	4067
rs770991465	snp	C/T			utr-variant-3-prime	LYN	GRCh38.p7	8:56012370	AATCCATACTCCCTA[C/T]CGCCAAGATTCTGAC	4067
rs771015674	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55997408	TTTATTTCCCACAGT[C/T]TAGGGGCAAGGAAAG	4067
rs771043198	snp	A/G	1.64787e-05	0.00287038	missense	LYN	GRCh38.p7	8:56010000	CTCTATGACATTATG[A/G]AAATGTGCTGGAAAG	4067
rs771049904	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55999797	ACCAACATGGAGAAA[A/C]CCCGTCTCTACTAAA	4067
rs771070459	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55917265	ATTGTAGGTCACTGC[A/C]GCCTTGAACTCCTAG	4067
rs771077655	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55950651	TGCCGTGGAACATAA[C/T]ATGCAGGAAATGTTG	4067
rs771115071	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55948887	GTGTTTAAACATGAC[A/G]TAAGCAAAGAGGATG	4067
rs771121756	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55968943	GCAGCACACTCCTTC[C/T]TAGGTAGGTTTCCAC	4067
rs771174377	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55928535	GTAGCTCTTCTTTGG[G/T]GAGGTGTCTATTCAG	4067
rs771178430	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55936565	GAATTGCTTGGGCCC[A/G]GGAGGCAGAGTTTGC	4067
rs771193955	snp	A/T	3.29565e-05	0.00405921	intron-variant	LYN	GRCh38.p7	8:55969686	TCTTGTGTGTTTGGA[A/T]TGCACTAACTTGTTC	4067
rs771211570	snp	C/T			intron-variant, downstream-variant-500B	LYN	GRCh38.p7	8:55968093	TTAAAGCAAACAAAC[C/T]AATTAGCTCTTGTGG	4067
rs771212623	snp	C/T	1.64754e-05	0.00287009	missense	LYN	GRCh38.p7	8:55947642	AACAAGGAGACATTG[C/T]GGTAGCCTTGTACCC	4067
rs771218096	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55954012	CTCGGGGATCTATGT[C/T]CTTCTAGAGATGGTG	4067
rs771231529	snp	A/G			intron-variant	LYN	GRCh38.p7	8:56009676	AACTTAGTTACCTCT[A/G]TAAAGGCCTTATCTC	4067
rs771232989	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55974820	TTTGATTGATAGCGT[C/T]CTCATGTTTAGTTCA	4067
rs771302754	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55913258	TTAAAGTTTGCTATG[C/T]TGCTTTCTTTCCAAA	4067
rs771360025	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55964278	TATATTGCCCAGGTT[A/G]GTCTTGAACTCCTGG	4067
rs771369754	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55911929	TTGATGGGGTGTGGT[A/G]GGCGTCCAAATGGAG	4067
rs771404548	in-del	-/CA			intron-variant	LYN	GRCh38.p7	8:55887572	ATATATATATATATA[-/CA]TATACACACACACAC	4067
rs771423666	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55881319	AAGCAGGGCCCAGTA[A/G]TCTGACTTTCCCTAA	4067
rs771427065	in-del	-/GGGCACAGTG			intron-variant	LYN	GRCh38.p7	8:55942642	ATACAAAAATTAGCT[-/GGGCACAGTG]GCGGGCGCCTGTAAT	4067
rs771466624	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55948493	GTGAGGACGCCTGAG[C/T]GTCGTCATCTCCTCA	4067
rs771498143	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55985017	TAAGGACTAGGGCCC[G/T]GAATAAGCCGCAGGG	4067
rs771519370	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55958867	TCATCTATTGATGGA[C/G]AATTAGGTTGTTTCT	4067
rs771532170	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55906674	GGTCAAGAATTTGAG[A/T]TCAGCTTGGGCAACG	4067
rs771539123	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55991596	GAGTTTCACCAGAAC[A/C]CCCCACCCCCAGGAT	4067
rs771540049	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55924897	CCCAGGCTGCAGTGC[A/G]GTGGTGCGATCGTGG	4067
rs771583704	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55905878	GCTCCTCTGTTCCTG[A/G]GACACACCTCTGGCA	4067
rs771605932	snp	A/G			intron-variant, utr-variant-3-prime	LYN	GRCh38.p7	8:55967929	AATGATCCAGGATTA[A/G]CAATCATCTCATGCA	4067
rs771619912	in-del	-/G			intron-variant	LYN	GRCh38.p7	8:55969533	TCACATCAGGTCAAA[-/G]GTAACAGATTAGAGG	4067
rs771633315	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55906455	ACTTCCACCTCCTGG[C/T]TTCAAGTGATTCACC	4067
rs771641177	snp	A/G	0.000417101	0.0144353	utr-variant-5-prime, missense	LYN	GRCh38.p7	8:55880054	CGCCCCCCACTCTGA[A/G]CTCAAGTCACCGTGG	4067
rs771671687	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55885723	CTCTGGAGAGGGAGG[A/T]CCACTTCTGCTTTCC	4067
rs771678566	snp	A/G			intron-variant	LYN	GRCh38.p7	8:56003744	AAATAAAAGAAAGGA[A/G]GAAAAAGAAAAAAGA	4067
rs771682643	in-del	-/G			intron-variant	LYN	GRCh38.p7	8:55981638	TGGGATTATAGGTGT[-/G]AGCCACCGTGCCCGG	4067
rs771684052	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55906271	CAGTGGCTCATGCCT[C/G]TAATACCAGTACTTT	4067
rs771684185	in-del	-/TATATATATATACACACACACACACACA			intron-variant	LYN	GRCh38.p7	8:55909000	GTATGTATATATATA[-/TATATATATATACACACACACACACACA]CACACACACACACAC	4067
rs771702918	in-del	-/TGTA	1.65321e-05	0.00287502	intron-variant	LYN	GRCh38.p7	8:55999581	TATTTACAATCAAGC[-/TGTA]TAAATGAGAAAAAGT	4067
rs771729477	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55959126	CAACAGTTGTTATTT[G/T]CTGTTTTGGGGATTT	4067
rs771740148	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55936302	ACTCATGGATCTGGA[A/G]CTTCCTCCACAGAAA	4067
rs771766572	snp	A/G	1.64882e-05	0.00287121	missense	LYN	GRCh38.p7	8:56009957	CCAGGGCTACAGGAT[A/G]CCCCGTGTGGAGAAC	4067
rs771778986	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55938948	AAGTCATCTGGCCGT[A/G]TGGTTTCTTCAAGGA	4067
rs771787913	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55963228	AGCTCTAGGGTGAGT[A/G]GGAGTGGATTTGCTG	4067
rs771792645	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55931129	TATATGTTACTTTTT[A/G]TATATAATAAAATAT	4067
rs771793789	snp	A/G	3.30972e-05	0.00406786	missense, intron-variant	LYN	GRCh38.p7	8:55941900	AAGACAGCTTGAGTG[A/G]CGATGGAGTAGATTT	4067
rs771821817	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55893591	TGACCTGTGGCATTT[C/G]TTAATCCATGAAGTC	4067
rs771885544	snp	A/G	1.64738e-05	0.00286995	intron-variant	LYN	GRCh38.p7	8:56009870	CCAGGTTTCTAAACG[A/G]CATGGGTTTCTGTTC	4067
rs771899158	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55941617	CCACAAGAATACGAG[C/T]AGAGTTAGAGCTGGA	4067
rs771916199	snp	A/G	5.14911e-05	0.00507375	intron-variant	LYN	GRCh38.p7	8:55950826	AAAACACTATTTAGG[A/G]AATTATTTTTAGAAA	4067
rs771927436	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55980904	TTCATCTTCCCAGAC[A/G]GAAGCTCTTTGCCCA	4067
rs771936326	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55971011	GGGAAAACCCAAGGG[A/T]GGGCAATGCCCATCC	4067
rs771992766	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55930052	CGTGAACTGCACATG[C/T]GAGGGATCTAAGTTA	4067
rs772001798	snp	A/G			intron-variant	LYN	GRCh38.p7	8:56009776	GCTGTTCAACCCCTA[A/G]CAGCCTCAGTAAAGC	4067
rs772009829	in-del	-/T			intron-variant	LYN	GRCh38.p7	8:55954544	CTACTTTAAAAAAAA[-/T]GTTTTTATAGTGAGC	4067
rs772027829	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55977947	ACAAAAGCAAACAGA[C/G]CTCGTCTCTAAAGGG	4067
rs772051218	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55903063	CATATCGGCCAGGCT[A/G]GTCTCGAACTCCTGA	4067
rs772052451	snp	C/T			intron-variant	LYN	GRCh38.p7	8:56007871	CCGCTTTTAATCCAG[C/T]ACTTTGGGAGGCCGA	4067
rs772079068	snp	A/G			intron-variant, utr-variant-3-prime	LYN	GRCh38.p7	8:55967996	ATTCAAAAGATGAAT[A/G]TTACATTTTCTTATT	4067
rs772106811	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55902638	CAGTAGTCCTATGAG[A/G]TAAGAGCTGAAAATT	4067
rs772161961	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55913324	CTAAGTCAAGTGAGT[A/G]TAAGAATTACCTATA	4067
rs772168729	in-del	-/GT			intron-variant	LYN	GRCh38.p7	8:55914101	AGGGTTGTTGTTGGT[-/GT]GTGTGTGTGTGTGTG	4067
rs772199223	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55924881	TGGAGTCTCTCTGTT[A/G]CCCAGGCTGCAGTGC	4067
rs772214038	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55970025	ATCTTCTATAAACCA[A/G]GTCAACCTCTTTATG	4067
rs772219074	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55927663	AACATGGTGAAACCC[A/T]GTCTCTATTAAAAAT	4067
rs772277814	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55967559	GAGCTCAGGCAATCT[A/G]CCTGCCTCAGCCTCT	4067
rs772346964	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55984779	TTCTTGGCTTCACTC[A/G]GAATGCAGGGGGAAG	4067
rs772363778	snp	G/T			intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55922630	AAATTAGCCGGGAGT[G/T]GTGGCACACGCCTGT	4067
rs772378608	snp	A/G	3.35689e-05	0.00409674	utr-variant-3-prime	LYN	GRCh38.p7	8:56010162	GCCTCATTTAGAGAG[A/G]AAAAGTAACCATCAC	4067
rs772407929	snp	G/T			upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55878644	CCATAGGATTCTTGA[G/T]AGGTTTCAATCACAC	4067
rs772408565	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55976904	CATTAAGGAAACTAG[G/T]CCGAGCACAGTGGCT	4067
rs772418308	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55938405	GACTACATCATCCAC[A/G]GCACTTGATATAAAG	4067
rs772468930	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55880394	GGTGGGAGGTGCGGG[A/C]GCGGGGGCGGGCTCA	4067
rs772477622	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55992217	CTAAGATGAAGAGAA[G/T]CTCCTCATTTGGTTT	4067
rs772484645	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55916152	TTCATGTTTAACTAA[A/G]TCTTCAGAAAAAATT	4067
rs772500686	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55954747	GGCTGAGGTGGGAGG[A/G]TCACTTAAGCCAAGG	4067
rs772507381	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55990913	CCCTGGGGAAAAAGT[C/T]ATTTGCAAAGTAAAT	4067
rs772524706	snp	G/T			upstream-variant-2KB, missense	LYN	GRCh38.p7	8:55879796	AAATCCGAGCACCAG[G/T]AAGTAGCTGGGACCT	4067
rs772527708	snp	A/G	1.6501e-05	0.00287232	intron-variant	LYN	GRCh38.p7	8:55950654	CGTGGAACATAATAT[A/G]CAGGAAATGTTGAAA	4067
rs772534446	snp	C/G/T	4.97437e-05	0.00498696	intron-variant	LYN	GRCh38.p7	8:55947754	CACGCCACGGCTGCT[C/G/T]GTTTCCTCAGGCCAC	4067
rs772540756	snp	C/T	1.64874e-05	0.00287113	synonymous-codon	LYN	GRCh38.p7	8:55998390	GAAGAACTACATTCA[C/T]CGGGACCTGCGAGCA	4067
rs772552463	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55913360	TGCTACAAATGCAAA[C/T]ATCCACAGCCTCCTT	4067
rs772561760	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55929746	AATACACAGAACTGT[C/T]CTCTAGAACAAATAA	4067
rs772574006	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55968888	GAAAAACAGGTCTTG[C/T]TTTAGAGATGAAGCC	4067
rs772577866	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55892011	ATTGTGGATTACAAA[C/G]TAAGGAGAAACTTCT	4067
rs772624538	snp	C/T	1.66178e-05	0.00288247	intron-variant	LYN	GRCh38.p7	8:55950456	TGTGTATTTCTATTC[C/T]AGGCATGGAGAATGG	4067
rs772632989	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55905727	GAGAGCCTCACTCCT[C/T]TCCCATCTGTTGGGA	4067
rs772643819	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55992248	AGAACCAAAAGATTT[C/T]ATCGGTTTCCCAAGC	4067
rs772648066	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55979624	CGGTTTGACTGAAAT[A/G]TGTATTCTGAGGTCA	4067
rs772667115	snp	A/C/T	3.29529e-05	0.00405901	intron-variant	LYN	GRCh38.p7	8:55969822	AAAGCCCCGTGTGCA[A/C/T]GTGCATTTGCAAAGA	4067
rs772694386	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55996250	TCAGGGAAGGCCCAC[A/G]GGGCAGAAGGTGAGG	4067
rs772740783	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55928389	GACCTCAGGTGATCC[A/G]CCGACCTTGGCCTCC	4067
rs772832021	snp	A/G	3.29603e-05	0.00405944	missense	LYN	GRCh38.p7	8:55998424	AATGTTCTGGTCTCC[A/G]AGTCACTCATGTGCA	4067
rs772837798	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55886485	ACACCTGACCTCAGG[A/T]GATCTGCCTGCCTCG	4067
rs772886036	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55953350	GTTTTAAATGGTTTT[G/T]CTTATATAAATTTCA	4067
rs772889192	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55885765	GTGTCACGGAGAGCA[C/G]AACTGTAGCCCGATG	4067
rs772916318	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55973910	ATGTGGCAAGAATCT[A/G]TCTCTTTAAAACAAA	4067
rs772918581	snp	A/G	3.29658e-05	0.00405978	intron-variant	LYN	GRCh38.p7	8:55999404	AAGTAAGAACCACAT[A/G]TCTTCTTCCTTAGGT	4067
rs772938697	in-del	-/AG			intron-variant	LYN	GRCh38.p7	8:55945424	TGAAGGATAGTATGC[-/AG]AGCCATGGGTTTTTC	4067
rs772957500	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55920458	ATAATGGGAAGTAAC[A/G]CATTGTTTACTTGCT	4067
rs772974101	in-del	-/T	1.73387e-05	0.00294432	intron-variant	LYN	GRCh38.p7	8:56009877	TCTAAACGGCATGGG[-/T]TTCTGTTCTTTTTGT	4067
rs772998819	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55963483	ATGTTGTCACAGAAG[A/C]TCTGCAATTGAATTT	4067
rs773010765	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55918572	CGATTGTTAAGGAAT[A/G]ATAATGCATTTTGTC	4067
rs773015677	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55969381	GGCAGGCCTTCCAGT[C/G]AGCTCGCTAAAGATT	4067
rs773056987	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55885839	CTTCCTCCACCCCAG[A/G]CCCCTGGGTCATTTG	4067
rs773080038	in-del	-/TG			intron-variant	LYN	GRCh38.p7	8:55916771	AATGGCACCTTAGGC[-/TG]TGTGTGTGTCAGACA	4067
rs773082600	snp	A/G	0.000165442	0.00909361	intron-variant, missense	LYN	GRCh38.p7	8:55941942	CAGTACGTAATACTG[A/G]AAGAACTATTTATGT	4067
rs773091224	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55934670	ACCCTGCATGAGACA[C/T]GAAGAGAAGAGAAGA	4067
rs773105775	snp	C/T			utr-variant-5-prime	LYN	GRCh38.p7	8:55877808	CCTCTGATCACTGCC[C/T]TCTGTGCTCAATTTA	4067
rs773133939	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55948932	AGTTCTAGTTGCCTT[C/G]ATGCCTTACAGACAA	4067
rs773259862	snp	C/T	1.65236e-05	0.00287429	synonymous-codon	LYN	GRCh38.p7	8:55953846	GAGCAGGCAGATGGC[C/T]TGTGCAGAAGATTGG	4067
rs773281831	snp	A/C	1.74233e-05	0.0029515	intron-variant	LYN	GRCh38.p7	8:55966941	CAAGGGCTTCAAACT[A/C]AAAAAGTAAAATGTG	4067
rs773295400	snp	A/G			intron-variant, utr-variant-3-prime	LYN	GRCh38.p7	8:55968016	ATTTTCTTATTTAAT[A/G]TCTGTGAGTATTTCA	4067
rs773299781	in-del	-/CA			intron-variant	LYN	GRCh38.p7	8:56003219	GCCCGCCACCACGCC[-/CA]CAGCTAATTTTTTTT	4067
rs773306278	snp	A/G			utr-variant-3-prime	LYN	GRCh38.p7	8:56012237	TTCCAGCCTCCCTGT[A/G]ACAGACAGGCATAAT	4067
rs773338249	in-del	-/AA			intron-variant	LYN	GRCh38.p7	8:55977753	TCCTATCTCTACCAA[-/AA]AAAAAAAAAAAAAAA	4067
rs773346419	snp	A/C			intron-variant	LYN	GRCh38.p7	8:56009624	TATAAGGATACTAGT[A/C]ATATTGGATTAAGAC	4067
rs773347139	in-del	-/TAAT			intron-variant	LYN	GRCh38.p7	8:55959235	TTTGTGTTTTCCTAA[-/TAAT]TAGTGACCAAGCATC	4067
rs773348954	snp	A/T	1.67248e-05	0.00289173	intron-variant	LYN	GRCh38.p7	8:55941811	GATGGCTTGAAGCAG[A/T]TCTGGAATGGTAAAA	4067
rs773373382	snp	C/T	5.16009e-05	0.00507915	intron-variant	LYN	GRCh38.p7	8:56009881	AACGGCATGGGTTTC[C/T]GTTCTTTTTGTTTTT	4067
rs773424991	snp	A/T			intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55923196	TAAGTAATTTAAAAA[A/T]TTTTTGAAACGAATT	4067
rs773445011	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55927704	GCTGTGTGTGGTGGC[A/G]GGTGCCTGTAATGCC	4067
rs773482741	in-del	-/AAAA			intron-variant	LYN	GRCh38.p7	8:55890333	AATAATAACAATAAT[-/AAAA]AGAAAGTTGCTTAGG	4067
rs773485609	snp	A/G	1.64798e-05	0.00287047	missense	LYN	GRCh38.p7	8:55947623	TCATCTTTAGATCCA[A/G]AGGAACAAGGAGACA	4067
rs773491595	snp	C/T			intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55923346	CCCAGCACATCTGCT[C/T]AGTTTCCGCCTCTCT	4067
rs773504413	in-del	-/CC			intron-variant	LYN	GRCh38.p7	8:55894055	CATCTTTCTGTGGGA[-/CC]CCCACTAAGGGACCC	4067
rs773545486	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55908004	TTGAAACCAAAACTT[A/C]AAGTTTTACTTGTTT	4067
rs773556563	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55966268	AGATACTTTTCATCT[A/G]GCCTCCCCTAATTTT	4067
rs773559286	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55976964	CCGAGGTGGGTGGAT[C/T]ACCTGAGGTCAGGAG	4067
rs773608708	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55977951	AAGCAAACAGAGCTC[A/G]TCTCTAAAGGGTACA	4067
rs773625238	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55983939	GGCCAGAAGTCTGGA[A/G]TGAAGGTATAGGCAG	4067
rs773687576	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55996268	GCAGAAGGTGAGGCC[A/G]GGGATTGGCCTAGAG	4067
rs773690890	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55963166	TGCTATGAACAATGC[A/G]CTGCACATTTTTGTG	4067
rs773754577	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55983044	AGCCCTATGGAAGTC[C/T]GACCCTTCACCTATT	4067
rs773822436	in-del	-/G			intron-variant	LYN	GRCh38.p7	8:55927142	TTCACTCTTGGTGTA[-/G]TACATTTCATGGATT	4067
rs773834119	in-del	-/A	1.64754e-05	0.00287009	intron-variant	LYN	GRCh38.p7	8:55969712	GTTCTTTCTTTCTCC[-/A]ATAGGCAGTTTGCTG	4067
rs773954370	in-del	-/T			intron-variant	LYN	GRCh38.p7	8:55979053	GCACTTCTCATTCTT[-/T]TTTTTTTTTTTTTTT	4067
rs773954952	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55950819	CTCTTTTAAAACACT[A/G]TTTAGGAAATTATTT	4067
rs773966262	snp	C/T			intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55923970	TATTCTCAAATGGGA[C/T]GTGTACACCCTGCCG	4067
rs773968926	snp	A/G	1.64757e-05	0.00287012	synonymous-codon	LYN	GRCh38.p7	8:55999449	TAAGTGGACGGCTCC[A/G]GAAGCAATCAACTTT	4067
rs773970021	snp	A/G	1.65056e-05	0.00287272	synonymous-codon	LYN	GRCh38.p7	8:55950693	CAGGTGGTTTTTCAA[A/G]GATATAACCAGGAAG	4067
rs773970110	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55911703	ACCTGCCCTGGAGAC[G/T]GAGGCAGGGAGTCAA	4067
rs773992136	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55896561	CCTAATGTAGATGAC[A/G]GGATGGTGGGTACAG	4067
rs774010425	snp	A/G			intron-variant	LYN	GRCh38.p7	8:56001988	AAAAATCATTTTTTG[A/G]AAAAAGAACTGGCTG	4067
rs774019696	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55970051	TTATGTTCATTTCAT[A/T]AGTCATAGAAACAGT	4067
rs774020813	snp	A/G			intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55923131	TGGTGAGAAAAAACA[A/G]TTTTCAGTAAGGAAG	4067
rs774023464	snp	A/G/T	0.000115788	0.00760792	intron-variant	LYN	GRCh38.p7	8:55999598	TATAAATGAGAAAAA[A/G/T]TCAGGTTGCATGAAG	4067
rs774025589	in-del	-/T			intron-variant	LYN	GRCh38.p7	8:55934348	GTCTGTCTTCCATCA[-/T]TACTGTTTCTTCTTC	4067
rs774043044	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55895789	CAAGGATTAAACGGG[A/G]TAATGTACCTGGGAG	4067
rs774049841	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55884559	CTCCTGGATTCAAGT[A/G]ATTCTCCTGCCTCAG	4067
rs774099114	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55962288	TGTGTTGGTGAGATG[A/C]ATCCATGCTTTTGGG	4067
rs774100994	in-del	-/G	1.66273e-05	0.00288329	intron-variant	LYN	GRCh38.p7	8:55942009	AAGTAGATAGTCTCA[-/G]GGGAGAATTCCCACA	4067
rs774108467	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55930026	GATTCTCATAGGGGC[A/G]TGAACCCCATCGTGA	4067
rs774155415	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55928828	GATCATTTTGATGTT[A/G]TATGTAAAATGTCAT	4067
rs774161268	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55941066	CTCAATTCATTTCCA[C/G]TCTTGATGAAAGCCA	4067
rs774164749	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55917300	ATGTGATCGTCCCGC[C/G]TCAGCCTCCCAAGTA	4067
rs774172219	in-del	-/TGTCTTTTTT			intron-variant	LYN	GRCh38.p7	8:55909990	GTGTGTGTGTGTGTG[-/TGTCTTTTTT]TTTTTTTTTTTGAGT	4067
rs774195758	snp	A/G	0.00011645	0.00762965	intron-variant	LYN	GRCh38.p7	8:55946444	AACAAATATTCTCTC[A/G]TAGGTTCCAGAATCT	4067
rs774201400	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55901830	GTTGCATTTCCTGGC[C/T]CAACCAAAGATAAGC	4067
rs774272454	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55996736	ACCTGACTTTGGAAC[G/T]ATACTACACTTTCTA	4067
rs774282765	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55953181	TGGTGACATGACCGA[A/G]TCCCCACTATGGTGC	4067
rs774302142	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55898381	GCAACCTCCGCCTTC[C/T]GTGTTCAAGCAATCC	4067
rs774351465	in-del	-/AT			intron-variant	LYN	GRCh38.p7	8:55942396	TATATATATATGTGT[-/AT]ATATATGTGTATATA	4067
rs774353009	in-del	-/TT			intron-variant	LYN	GRCh38.p7	8:55900541	CCATGCCCAGCTAAT[-/TT]TTTTTTTTTTTTTTT	4067
rs774354225	snp	A/G	1.64811e-05	0.00287059	synonymous-codon	LYN	GRCh38.p7	8:56010053	GTTTGACTACTTACA[A/G]AGCGTCCTGGATGAT	4067
rs774358892	snp	C/T			utr-variant-3-prime	LYN	GRCh38.p7	8:56011082	TATTAATTTTAGTTG[C/T]ACTCTAGAAAGCTAA	4067
rs774418244	snp	A/C			intron-variant	LYN	GRCh38.p7	8:56007179	AAGGAAGTGAAAGAG[A/C]TATTCCAAACTGAGT	4067
rs774424836	in-del	-/AAAAGAAAGAAAG			intron-variant	LYN	GRCh38.p7	8:55905415	ACTCCGTCTCAAAAA[-/AAAAGAAAGAAAG]AAAGAAAGAAAGAAA	4067
rs774442099	snp	G/T	1.66145e-05	0.00288218	utr-variant-3-prime	LYN	GRCh38.p7	8:56010135	AGACCCGTCCATTTG[G/T]CAGGGGTGGCTGCCT	4067
rs774443127	snp	C/T	1.64789e-05	0.0028704	missense	LYN	GRCh38.p7	8:56010004	ATGACATTATGAAAA[C/T]GTGCTGGAAAGAAAA	4067
rs774466341	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55926479	CATAAATGGCTATGG[A/G]CGTATTAGGAGTGAT	4067
rs774468158	in-del	-/GGACACGA			intron-variant	LYN	GRCh38.p7	8:55995375	TGGGAGAAAGGCAGG[-/GGACACGA]AGTCACTGCTCTCCA	4067
rs774473977	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55975110	AGAGGAATCTGAGCC[A/G]GGTGCCGCTGTGGAT	4067
rs774489645	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55912285	AACAAAATGTTTTTC[A/G]TAATGAAGTGGTTAT	4067
rs774526198	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55888158	AACTTTTCCTGGGTA[A/G]CTACTGGGAGTCCCG	4067
rs774535026	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55966120	ACAGAGCAAGACGTA[A/G]TCTAAAAATAAATAA	4067
rs774601248	snp	A/G	1.65726e-05	0.00287855	intron-variant	LYN	GRCh38.p7	8:55947751	AAGCACGCCACGGCT[A/G]CTCGTTTCCTCAGGC	4067
rs774603134	in-del	-/AAAA			intron-variant	LYN	GRCh38.p7	8:55912727	TGAGACTCCATCTGA[-/AAAA]AAAAAAAAAACAAAA	4067
rs774615840	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55944457	AGGTTTTAAAACACA[A/G]GTTTTTTCGTTTTGC	4067
rs774655064	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55949478	AGATGTTCTCCACCC[A/G]CCTTCACCATCCTAA	4067
rs774655297	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55936575	GGCCCGGGAGGCAGA[A/G]TTTGCAGTGAGCAGA	4067
rs774661641	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55904709	GAGCCGAGATTGCAC[C/T]ACTGCTCTCCAGCCT	4067
rs774711116	snp	A/G	1.64751e-05	0.00287007	missense	LYN	GRCh38.p7	8:55947647	GGAGACATTGTGGTA[A/G]CCTTGTACCCCTATG	4067
rs774735125	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55956650	TCCCTCTTAGAAGCC[A/G]TCACTTCTCTATAAA	4067
rs774762324	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55945609	TAGGCCTCTGACAGC[A/C]TCTATCTTACAAGAG	4067
rs774783453	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55927340	CGGTTGGAATCACAC[A/G]GTATGTAGCCTTTTC	4067
rs774800002	snp	C/T	1.64746e-05	0.00287002	intron-variant	LYN	GRCh38.p7	8:55969812	ACATATTCAAAAAGC[C/T]CCGTGTGCACGTGCA	4067
rs774931672	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55960964	TCTGTGGATTGTCCT[A/G]TTCCCAGGGAATCAA	4067
rs774932762	snp	C/G			intron-variant	LYN	GRCh38.p7	8:56001170	TGGGGAGAGCAGCCA[C/G]AGCATGGGCTTGGCC	4067
rs774979105	snp	A/C	3.29582e-05	0.00405931	intron-variant	LYN	GRCh38.p7	8:55969689	TGTGTGTTTGGAATG[A/C]ACTAACTTGTTCTTT	4067
rs774984652	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55962085	TCTTTTACTCAACGG[G/T]TTGGTGAGAGGCATC	4067
rs774986192	snp	C/T			utr-variant-5-prime	LYN	GRCh38.p7	8:55877713	ACAATACCGCCTTCT[C/T]TTGCCCCGCCCATCG	4067
rs774986532	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55904624	GTGCGGTGGCTCATG[C/T]CTGTAATCCCAGCTA	4067
rs775019989	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55883503	ACTGCTAAGATGACA[C/G]CTATACTGGCTGCTG	4067
rs775025206	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55981847	TGTGGGAAAAACAAA[C/G]TGCAGCTTTGTTTTG	4067
rs775042756	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55982698	TTCCATCATTTGTAG[C/T]CATCCCCACCTTCAA	4067
rs775061526	in-del	-/GT			intron-variant	LYN	GRCh38.p7	8:55988292	TTTGCAAACTCCCTG[-/GT]GTGTGTGTGTGTGTG	4067
rs775072946	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55894986	CAGTGCCAAGCCTAA[A/G]ATTTTTTGTATAGTT	4067
rs775073766	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55956675	TATAAAGCTCCAGTC[A/C]TTTCTGTCCTCCTCC	4067
rs775079772	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55975823	TTTTTTTGGTAAGGT[C/G]GGGGTGGGGCTGTTT	4067
rs775082693	snp	A/C			downstream-variant-500B	LYN	GRCh38.p7	8:56012608	CCTATGGTCCCAGCT[A/C]CTCAGGAGGCTGAGG	4067
rs775110974	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55921388	GTCTATCGAGGAGAG[A/C]GCTATACACGTACTA	4067
rs775130607	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55939625	TGGATCGAGCGGCCC[A/G]GTGCGCTGTGGGTTG	4067
rs775144778	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55944122	AAAGAGTGGATATAT[C/T]ATGCTATTAAGTTAT	4067
rs775176903	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55932418	TATATATATTTTTTG[G/T]TTGTTTGTTTTTGTT	4067
rs775207795	in-del	-/A			intron-variant	LYN	GRCh38.p7	8:55982317	TTTTGTTTTTTTTTT[-/A]AATCCTCAGATTTTT	4067
rs775240936	snp	A/C			utr-variant-5-prime	LYN	GRCh38.p7	8:55877636	AAATACATTTTAGCA[A/C]GTAGATAAGTTCACA	4067
rs775241950	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55901390	GTGATGGTATTTTTA[C/T]ATTGACTTTAATATG	4067
rs775246919	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55971200	AACAGAGGGGCAAGG[A/G]AAGGACCCAGCAGCC	4067
rs775272242	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55988143	TCCAAATTATGGATT[A/G]GAGATTAGAGGAATC	4067
rs775326275	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55880780	CGAGAGTTATTTTAA[C/G]AATTCAGGGGTTGCC	4067
rs775346076	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55910264	AGATTTTCTTCTAGT[A/G]TTTTTATGCTTTCAT	4067
rs775351023	snp	C/T	0.000115364	0.00759399	intron-variant	LYN	GRCh38.p7	8:55950602	GCTTTATTTGCCACA[C/T]TGGATTTCTTGTTAA	4067
rs775354251	snp	C/T	1.74659e-05	0.0029551	intron-variant	LYN	GRCh38.p7	8:56009871	CAGGTTTCTAAACGG[C/T]ATGGGTTTCTGTTCT	4067
rs775364308	snp	A/C	1.66905e-05	0.00288876	intron-variant	LYN	GRCh38.p7	8:55941833	ATGGTAAAACAATGT[A/C]ATTACTTTTATGTTT	4067
rs775380138	snp	C/T	8.23839e-05	0.00641757	synonymous-codon	LYN	GRCh38.p7	8:55952024	TGATGTTATTAAGCA[C/T]TACAAAATTAGAAGT	4067
rs775388152	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55938580	GCAGACCTGTTCCCT[A/G]CAATGTTACCACATT	4067
rs775432707	in-del	-/TC			intron-variant	LYN	GRCh38.p7	8:55938722	AGCCTATAAAAATAA[-/TC]TCTTTGTTTGGCATT	4067
rs775448775	snp	C/T	9.9295e-05	0.0070454	synonymous-codon, intron-variant	LYN	GRCh38.p7	8:55941901	AGACAGCTTGAGTGA[C/T]GATGGAGTAGATTTG	4067
rs775480217	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55985908	TCAGTGGCTCATGTC[C/T]GTAATCCCAACATTT	4067
rs775508347	in-del	-/CT			intron-variant	LYN	GRCh38.p7	8:55907463	GAGGTGTCAAGGAAG[-/CT]CTGTGTCTGGTTTTG	4067
rs775550146	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55997728	AAACTGGCATAATAA[C/T]ATCTATGTATCTACA	4067
rs775573672	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55965498	TATTGTACTTTAAAG[G/T]TAGTATATATAAGTA	4067
rs775574254	snp	A/G	4.95495e-05	0.00497718	intron-variant	LYN	GRCh38.p7	8:55954000	GTAAGTGTGCGGCTC[A/G]GGGATCTATGTCCTT	4067
rs775601129	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55907979	TTATTACCTTAGCAG[A/T]TTGTAAGGGTTGAAA	4067
rs775615847	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55893299	TGCACAGCCAAGTCA[A/G]TTTATAAATGCAAAT	4067
rs775626544	snp	A/C			intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55922942	TAGAGAAAGGAGACC[A/C]ATATAGGGAAAAGAA	4067
rs775664195	snp	A/C	1.65608e-05	0.00287752	intron-variant, synonymous-codon	LYN	GRCh38.p7	8:55941967	TTATGTGAGAGATCC[A/C]ACGTCCAATAAACAG	4067
rs775678175	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55881507	GTCCCTCCATTCTCA[C/T]TTGGAGGTAAGCAGG	4067
rs775732257	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55926157	CAGCAGATTCCTGCC[C/T]TACCTTCCTGAAGCC	4067
rs775747286	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55948647	TGTCACTGTGACCTG[A/C]CAAATAGGGTTTGAG	4067
rs775800319	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55959058	TACTTCGGCTGCACC[A/G]TTTTACATTCCCATT	4067
rs775809489	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55999339	AAAAGAAAAGAAAAG[A/G]AAGTATGGGGTCACA	4067
rs775864874	in-del	-/C			utr-variant-3-prime	LYN	GRCh38.p7	8:56010731	TGCTCAGACCTGCTA[-/C]GACATGCCATAGGAG	4067
rs775901867	in-del	-/ACACAT/ACAT			intron-variant	LYN	GRCh38.p7	8:55887603	CACACACACACACAC[-/ACACAT/ACAT]ATATATATATATTTT	4067
rs775911865	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55955679	CAATAAACAATCACT[C/T]TTCATTCGCCCCACC	4067
rs775920259	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55906277	CTCATGCCTGTAATA[C/T]CAGTACTTTGGGAGG	4067
rs775927161	in-del	-/T			intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55923714	CACCTGATTTTTGTA[-/T]TTTTTAGTAGAGATG	4067
rs775941123	snp	G/T	1.65644e-05	0.00287783	missense	LYN	GRCh38.p7	8:55950462	TTTCTATTCTAGGCA[G/T]GGAGAATGGTGGAAA	4067
rs775942701	snp	C/T	1.64811e-05	0.00287059	missense	LYN	GRCh38.p7	8:55998416	GAGCAGCTAATGTTC[C/T]GGTCTCCGAGTCACT	4067
rs775954981	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55903735	GAATTTAAAGTGTTT[C/T]ATCCATGGTAGCTCA	4067
rs775959692	in-del	-/T			intron-variant	LYN	GRCh38.p7	8:55890730	ATGTACATTGGAATT[-/T]TTTTTTTTTTTTTTT	4067
rs775970552	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55974941	CCAGGAGGCCAGATC[C/T]GCTCCCCACTCCATA	4067
rs775984206	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55942917	ACTTTATCCTGTCCT[G/T]TCATTTCTTCAATTA	4067
rs775985657	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55931707	ATATATGTATTAAAA[G/T]TTAATAGTCACTTAG	4067
rs776030927	snp	C/T	1.6477e-05	0.00287024	missense	LYN	GRCh38.p7	8:55950512	AAAAAGAAGGCTTCA[C/T]CCCCAGCAACTATGT	4067
rs776061471	snp	C/T			utr-variant-3-prime	LYN	GRCh38.p7	8:56012313	GTGCAAAATGGCTCA[C/T]GTCATCACACCTCAG	4067
rs776064555	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55970520	TTTCTCAGTATTGGC[A/G]ATCGGTGGTTTCATG	4067
rs776106617	snp	A/G			intron-variant	LYN	GRCh38.p7	8:56005956	AGAGTATGGTGGTAC[A/G]CACCTGTAGTCTCAG	4067
rs776158163	snp	C/T			intron-variant	LYN	GRCh38.p7	8:56007028	CTTTACCAGCATCAT[C/T]GAGAGTCCTTCAGAG	4067
rs776189088	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55898290	AACAGCTTTATTTTT[A/G]CTTTTAATTTTGTTT	4067
rs776209515	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55950937	ACAAACCTCAGTGAT[C/T]AGTTGTGCTACTAAA	4067
rs776227403	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55997838	GCCTGTAATCCCAGC[A/T]CTTTGGGAGGCCAAG	4067
rs776276450	snp	A/G	0.000724948	0.0190249	synonymous-codon	LYN	GRCh38.p7	8:55950498	GTCCCTTTTAACAAA[A/G]AAAGAAGGCTTCATC	4067
rs776326334	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55992301	CCAGAGCTGTGATAG[A/G]GAGGGAGAGGAGCTG	4067
rs776337043	snp	C/G			upstream-variant-2KB	LYN	GRCh38.p7	8:55876792	CCAACATGAACAGGT[C/G]AGCAGCATGACCAAT	4067
rs776363867	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55941148	ATTCTAGCTCTTCAT[C/T]ACCTGCCCTTGAAGT	4067
rs776370617	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55962015	TAGCTCAGTTTTGCT[G/T]TTTTTGTACTTTGTA	4067
rs776381414	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55981085	CTGTGCATGTGACTG[A/T]TTCCTCAGCACTGAG	4067
rs776401006	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55913489	CCAACTTGAATAAAA[C/T]GATTAAAGTTGTGCT	4067
rs776409265	snp	G/T	1.6483e-05	0.00287076	intron-variant	LYN	GRCh38.p7	8:55969840	GCATTTGCAAAGACT[G/T]CCCTGCGTCAAATTC	4067
rs776438526	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55973749	TGCAAAAATTACTAA[A/T]AATGGAACAATTGTT	4067
rs776498382	snp	C/T	1.6691e-05	0.00288881	intron-variant	LYN	GRCh38.p7	8:55953820	AACCTTCATTTTTCC[C/T]TTTCAAATTAGAGCA	4067
rs776501780	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55921273	CAACTGGTGCTTTGT[A/T]GCTGACTTGGTAACC	4067
rs776502411	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55987995	TTCACTATTTCTTAG[A/C]AGTTATACTTGGAAA	4067
rs776505762	snp	A/T	0.00017751	0.0094193	intron-variant	LYN	GRCh38.p7	8:55880120	TGAGTCCTCTGCGCG[A/T]GCCCAGGGGTGGGCG	4067
rs776628117	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55997430	CAAGGAAAGCCCTGG[A/C]AGGTTTCATGTCTGA	4067
rs776630083	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55983990	GGGAAGAATCCTTCC[A/G]TACCTCTTCCAGCTT	4067
rs776660567	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55911194	ATATATATATACACA[C/T]ACACATATATATATA	4067
rs776671670	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55925179	CCAGGCTAGGGTGCA[A/G]TGGTGCAATCACCGT	4067
rs776683800	snp	A/G			intron-variant	LYN	GRCh38.p7	8:56009857	GCTTGACCCTCTGCC[A/G]GGTTTCTAAACGGCA	4067
rs776701250	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55933233	CTAATATGACATTAC[A/G]TAAATCTGAAATAAT	4067
rs776701671	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55904534	TAGGGCATGGAATTA[C/T]GATGCCACACAAAAT	4067
rs776703109	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55985085	GAGAAGTTGCTGAAC[C/T]GAGCAAGTGATCCTT	4067
rs776719521	snp	C/T	3.32884e-05	0.00407959	missense	LYN	GRCh38.p7	8:55946458	CGTAGGTTCCAGAAT[C/T]TCAGCTTTTACCTGG	4067
rs776745731	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55894851	GCCTGGCTAATTTTT[C/G]TATTTTTTGTAGAGA	4067
rs776760526	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55947244	ACAAGAGCGAGACTC[C/T]GTCTCAAAAGAGAAA	4067
rs776780392	snp	C/T	1.64825e-05	0.00287071	synonymous-codon	LYN	GRCh38.p7	8:55952063	TGGGGGCTATTACAT[C/T]TCTCCACGAATCACT	4067
rs776788142	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55942008	TAAGTAGATAGTCTC[A/G]GGGGAGAATTCCCAC	4067
rs776800395	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55886537	ACAGGCATGAGCCAC[A/G]CGCCCAGCCTGTCAA	4067
rs776811005	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55905922	CCCATTCATCTTGAC[C/T]TCTGGAAAGAAGCCT	4067
rs776812594	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55964301	ACTCCTGGGCTCAAG[C/T]GATCCTCCTGCCTCT	4067
rs776832330	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55892271	TCTAAAAATCCAAAA[A/G]TAGCCAGGTGTGGTG	4067
rs776841850	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55895710	GAAGCTCCTTCATCT[A/T]ATGTTTTTCTAATAC	4067
rs776843044	in-del	-/A			intron-variant	LYN	GRCh38.p7	8:55917175	AGTGAGATTCTGTCT[-/A]AAAAAAAAAAAAAAG	4067
rs776908593	snp	A/G	1.64817e-05	0.00287064	missense	LYN	GRCh38.p7	8:55966798	TTCCTGGAAGAAGCC[A/G]ACCTCATGAAGACCC	4067
rs776937514	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55948496	AGGACGCCTGAGTGT[C/T]GTCATCTCCTCAACC	4067
rs776951765	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55925050	TTTCACCATGTTGGC[C/T]AAACTGGGGTGATCC	4067
rs776966837	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55908344	CTGCCTCCCAGGTTC[A/G]AGTGATTCTCCTGCT	4067
rs776983165	in-del	-/TAC			intron-variant	LYN	GRCh38.p7	8:56008162	ATAAAATACTGGTAG[-/TAC]TACTCTAAAAAAGTC	4067
rs776985141	in-del	-/G			intron-variant	LYN	GRCh38.p7	8:55927124	CTACAGTTTTCATTA[-/G]GATTCACTCTTGGTG	4067
rs777006723	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55924401	GGAGTCTTGCTCTAT[A/G]ATCCAGGCTGGAGTG	4067
rs777038552	in-del	-/CAAA			upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55879109	CACACATTCTTTCAG[-/CAAA]CACTGGTTAGGCACC	4067
rs777105867	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55951338	TTGCTGAGCCTTTTG[C/T]ATTATTATTTGAATA	4067
rs777121745	in-del	-/G			intron-variant	LYN	GRCh38.p7	8:55881111	TTTAGTACACACAAA[-/G]CCCCTAGTACGTACC	4067
rs777164782	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55924899	CAGGCTGCAGTGCGG[G/T]GGTGCGATCGTGGCT	4067
rs777183857	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55973379	ACTACAGCAGCTTTA[C/G]CCACTGCTTTTCTCT	4067
rs777201721	snp	C/T			intron-variant	LYN	GRCh38.p7	8:56005660	TTAAGTTTCTATTTC[C/T]TGTTCTCTTTTTTGT	4067
rs777209156	snp	C/T	1.65364e-05	0.0028754	intron-variant	LYN	GRCh38.p7	8:55999589	ATCAAGCTGTATAAA[C/T]GAGAAAAAGTCAGGT	4067
rs777243458	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55896708	ATACCTAATTTAGTA[A/G]GAGAGGCATTCCCCC	4067
rs777291176	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55985970	CCAGGAGTTCGAGAC[A/C]CGCCTGGGCAATATA	4067
rs777296861	snp	A/C/T	6.61359e-05	0.00575017	missense, synonymous-codon	LYN	GRCh38.p7	8:56009924	GAGAACTAATGCCGA[A/C/T]GTGATGACCGCCCTG	4067
rs777300791	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55925903	ACAGAAGCATACAAG[A/T]GTTTATGTAAAAATT	4067
rs777326608	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55906775	AAATAAATGAAATGT[A/T]TCCCAGTTGAACAAC	4067
rs777368578	in-del	-/AAAAAAAAAAAAAA			intron-variant	LYN	GRCh38.p7	8:55990242	GAGACTCTGCCTCCA[-/AAAAAAAAAAAAAA]AAAAAAAAAGTCCTG	4067
rs777396577	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55933091	TGTAACAAACCTGCA[C/T]ATGTATTCCTGAACC	4067
rs777406754	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55954435	TCACGTCATGAAGAA[A/G]TCATTTCTTAACATT	4067
rs777439829	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55990038	GAGGTCAGGAGTTTG[A/T]GACCAGCCTGGCCAA	4067
rs777494971	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55982321	TGTTTTTTTTTTAAT[C/T]CTCAGATTTTTGAAT	4067
rs777496721	in-del	-/A			intron-variant	LYN	GRCh38.p7	8:55886138	TTTAATGTTCAGGCT[-/A]ACATAATAATTTTTA	4067
rs777525026	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55939001	TATAAATGTGTAATA[C/G]AAGAATACTAAGGTG	4067
rs777543805	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55906438	GATTTCGGTTCACTG[A/C]AACTTCCACCTCCTG	4067
rs777552056	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55971873	GAGAAGCTACTTTCT[A/G]GACCTTCATAGCTTA	4067
rs777556531	snp	C/T			intron-variant	LYN	GRCh38.p7	8:56007713	ATTGTGGGAAATACA[C/T]AGAAACCTACTCTGT	4067
rs777567059	snp	A/T	8.52958e-05	0.00652998	intron-variant	LYN	GRCh38.p7	8:55966706	GCCCGCCTTCTTTTT[A/T]CTTCCTAGGTTACTA	4067
rs777570673	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55915476	TTCGGAAGCCAAGGC[A/G]GGCGGATCACCTGAG	4067
rs777595664	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55944942	GCTTGAAGTCTTTCA[A/G]TTCCCTCCTGTATAC	4067
rs777613702	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55994344	CCTGTCTTGGTGAAC[A/G]CTTTAATTACTGTTT	4067
rs777614769	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55941583	GGGTCCTCTGTCATC[A/G]AGTCTTTACACATCT	4067
rs777619051	snp	G/T	0.000136017	0.00824562	intron-variant	LYN	GRCh38.p7	8:55946545	CTTTACTATTAGAGC[G/T]TCTATAAAGTGATTG	4067
rs777649651	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55904410	TATTTACAATCCTGG[A/G]TTCTATTTGTCAATC	4067
rs777652351	snp	C/G			upstream-variant-2KB	LYN	GRCh38.p7	8:55877303	GGGTCTCACGATATT[C/G]CCTAGGATGGTCTTG	4067
rs777674520	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55992991	CAGACCATAGCATCA[C/T]GCATTTGCAGTGGGG	4067
rs777685113	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55940439	GGAGTGCAGTGGCGC[A/G]ATCTCGGCTCACTGC	4067
rs777741329	snp	G/T	1.66261e-05	0.00288319	intron-variant	LYN	GRCh38.p7	8:55946415	AAGAAAAGCTAAACA[G/T]AATTTTTTTTTCTAA	4067
rs777742447	snp	A/C			missense	LYN	GRCh38.p7	8:56010105	CAATACCAGCAGCAG[A/C]CTTAGAGCACAGGGA	4067
rs777812224	in-del	-/TTTA	1.64808e-05	0.00287057	intron-variant	LYN	GRCh38.p7	8:55950589	TGTCATCTTGGTGGC[-/TTTA]TTTGCCACATTGGAT	4067
rs777812419	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55914321	GGGGCCAGTCCTGCT[A/G]CTCCCTGTAAGCACT	4067
rs777829006	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55986565	TGAAAATCATCTCTC[C/G]CTAAGGCATTGTGGG	4067
rs777839400	in-del	-/AT			intron-variant, downstream-variant-500B	LYN	GRCh38.p7	8:55968250	ATGTAACAATGCCTA[-/AT]ATATATATATATTTA	4067
rs777860372	snp	A/G	1.6888e-05	0.00290581	intron-variant	LYN	GRCh38.p7	8:55950421	TGCATGGAGTATGTA[A/G]TCTTTTAGCTTCTTT	4067
rs777908975	in-del	-/AA			intron-variant	LYN	GRCh38.p7	8:55977752	ACTCCTATCTCTACC[-/AA]AAAAAAAAAAAAAAA	4067
rs777952110	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55978987	CTGACCGCTCAGCAT[A/G]CCTCACTCTTGAAAA	4067
rs777985373	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55951078	CAAGACCCCATCTCT[A/G]CAAGAAATACAAAAC	4067
rs778024291	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55970173	TAAGTTACGAATCGA[A/G]TGTATGGATACTTTT	4067
rs778035246	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55963798	ATATCCTGGATGCAA[G/T]TTCCTTGCAGTTATA	4067
rs778088270	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55948390	TGTTTAGACTGGGTT[C/T]ATGGGCCCAGCCTAG	4067
rs778105987	in-del	-/TA			intron-variant	LYN	GRCh38.p7	8:55942358	GTGTATATATATGTG[-/TA]TATATATGTGTATAT	4067
rs778107999	snp	C/T			intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55923567	TTTTTTGAGACAGGG[C/T]CTTGCTCTGTCCCCA	4067
rs778108551	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55995712	GGGAATGAGCGTTCC[A/T]CACAGAGGCAGGGGG	4067
rs778115790	snp	A/T			upstream-variant-2KB, missense	LYN	GRCh38.p7	8:55879811	GAAGTAGCTGGGACC[A/T]CTCGGCCGAGCCCAG	4067
rs778117982	snp	C/T	3.29473e-05	0.00405864	synonymous-codon	LYN	GRCh38.p7	8:55969775	GCTGCTTCCAAAGCT[C/T]ATTGACTTTTCTGCT	4067
rs778120809	in-del	-/TAT			intron-variant	LYN	GRCh38.p7	8:55887612	ACACACATATATATA[-/TAT]TATTTTTTTTTTCCT	4067
rs778146993	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55906513	ATGTGCCCACCACCA[C/G]GCCCAGCTAATTTTT	4067
rs778166548	in-del	-/C			intron-variant	LYN	GRCh38.p7	8:56005156	CTCTATTCCCAGCCA[-/C]ACAATTCTCTCCCCA	4067
rs778175703	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55885335	TTTTTAGTTGGTCTC[A/C]TTTCCTTTCTACAGT	4067
rs778184267	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55991110	CTCTGAGATGCTGCT[C/T]GGGGTCTGAGGTCTA	4067
rs778205931	snp	A/G	0.000200662	0.0100145	utr-variant-5-prime, missense	LYN	GRCh38.p7	8:55879862	GCCGCGCCGGGCCGC[A/G]CTGCCGCTCGCTCCC	4067
rs778230647	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55958620	ACTCTTTAACACCAA[C/T]TCCCTGATCCCCTCT	4067
rs778235345	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55919509	GATTTTACCATGGAG[A/G]GATGGGATGGGCCAC	4067
rs778257744	in-del	-/AAATT			intron-variant	LYN	GRCh38.p7	8:56002604	GAGACTCCATCTCAA[-/AAATT]AAATTAAATTAAATT	4067
rs778263382	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55881077	CATCTTTGAGAGAGC[A/G]TATATACCTCAGGGG	4067
rs778286570	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55997334	CCAACTCTATTTTCA[C/T]AGTTGGTTCAGGCTG	4067
rs778290305	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55918109	GCAGCAGCAGCTTGC[A/G]GATCTCCCAGCGCTG	4067
rs778297574	in-del	-/GA			intron-variant	LYN	GRCh38.p7	8:55932656	AACTCCTAACCTCAG[-/GA]GTGATCCTCCTGCCC	4067
rs778300668	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55993869	ACCAACTCCATGTAA[C/T]TCCCACAGAAGTCAA	4067
rs778318597	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55892880	TAGCTGAATGCAAAG[A/C]CTTGTGTAACCACCC	4067
rs778333949	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55897079	AATAACTGCAATGGA[A/G]TGAGCTGGTTGGAGA	4067
rs778427830	snp	C/G	1.71971e-05	0.00293227	intron-variant	LYN	GRCh38.p7	8:55952156	AGACAAGATATATTT[C/G]TTATGATATGTATAA	4067
rs778430140	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55906385	AGAGTTTCAATCTGT[C/G]GCCCAGACTGGAGTG	4067
rs778451281	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55936016	CTGAGTCTCCTTTCC[A/G]AAAGTAAAGTAAGAA	4067
rs778459539	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55887350	TTTCTGAAATAAAAT[A/G]TTCATATATGGACAC	4067
rs778486517	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55929587	CAATTAAAACATCAG[A/G]TTTCCTGGCATGAAG	4067
rs778487640	snp	G/T	6.6036e-05	0.00574575	missense	LYN	GRCh38.p7	8:56009934	GCCGACGTGATGACC[G/T]CCCTGTCCCAGGGCT	4067
rs778520193	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55980459	GCAAAGTGCAGCCCA[C/G]AGCTCCTGGGCTCAA	4067
rs778572673	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55974727	GTAAGAGATGTGTTA[A/G]ACGCTCATATTCCAC	4067
rs778579501	snp	A/G	1.6476e-05	0.00287014	missense	LYN	GRCh38.p7	8:55947681	GCATCCACCCGGACG[A/G]CTTGTCTTTCAAGAA	4067
rs778630152	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55992928	CCCCCCCTCTTAATA[C/T]GATTGCATTGGAGAT	4067
rs778652763	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55941608	ACATCTTTGCCACAA[A/G]AATACGAGCAGAGTT	4067
rs778674557	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55880874	ATGGTGGCATCTTTT[G/T]CTTGCGGTGCATTCG	4067
rs778727915	snp	A/G					GRCh38.p7	8:55879493	GAGCGCACCTCCTCC[A/G]CTCCTGGGAGCACCC	4067
rs778757808	snp	A/C					GRCh38.p7	8:55903002	TACAGGTGTGTGCCA[A/C]CACACCCAGCTAATT	4067
rs778759820	snp	C/T	1.65233e-05	0.00287426			GRCh38.p7	8:55947577	GTTAAAACGCTTCTG[C/T]TGATGGATTCTTACA	4067
rs778787203	in-del	-/A			intron-variant	LYN	GRCh38.p7	8:55979410	AATTACTGAGAGAGG[-/A]ACTTAAATTATTGGT	4067
rs778797930	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55887365	ATTCATATATGGACA[C/T]ATCATCTATAAACTG	4067
rs778802303	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55989173	GAGCTTGCTGGAAGC[C/T]GGTTTCACCGTGTGG	4067
rs778829034	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55962731	TGGAGTTCATGTTAG[A/T]CCATTTTGCTTTGCT	4067
rs778871251	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55950334	TGTTTTCTTTATTTT[G/T]AATTTTTTAATTGAT	4067
rs778922925	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55885060	TTCTTCTGCTCTCCC[C/T]ACTTCATTCCCTATC	4067
rs778952064	snp	C/T	0.000117056	0.00764946	intron-variant	LYN	GRCh38.p7	8:55966907	CCAAGGGTGAGTTCC[C/T]CCCACTGCCCAGAGC	4067
rs779048759	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55924835	TTCAAGCTTAGTCCA[A/G]AGAATGGTTTCCCTT	4067
rs779113955	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55938350	ACGCATAAAATATGT[A/C]TTTATTTACTGTTCA	4067
rs779143722	in-del	-/TG			intron-variant	LYN	GRCh38.p7	8:55965730	ATGTGAGTGTATGCC[-/TG]TGTGTGTGTATGTAT	4067
rs779160056	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55921191	AAAATATATTCTATT[A/T]CGGAATTGCTGCTGA	4067
rs779164317	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55972435	ATTTGAGAAAGGGGT[C/G]TTACCCTTGGCAACA	4067
rs779164931	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55950291	TATATGTCAAGGAGT[A/G]TAGTTGCTGGGTCCT	4067
rs779172066	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55884152	TCGCCCAGCCTGGAG[A/T]GCAGTGGTGCAATCT	4067
rs779174451	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55967417	CCTCCCGGGTTCAAG[C/G]GATTCTCCTGCCTCG	4067
rs779175294	snp	C/G			intron-variant	LYN	GRCh38.p7	8:56007244	TGTTAGTCCTCCCAC[C/G]ACGATCCCAGAATTT	4067
rs779219387	snp	A/C			utr-variant-5-prime, synonymous-codon	LYN	GRCh38.p7	8:55880097	CCGAAACTTTCACCG[A/C]GAGCGGGTGAGTCCT	4067
rs779233456	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55957700	GTAATCCTGGCACTT[C/T]GGGAGGCCGAGGCAG	4067
rs779237059	snp	C/T	1.6646e-05	0.00288491	intron-variant	LYN	GRCh38.p7	8:55950453	TGATGTGTATTTCTA[C/T]TCTAGGCATGGAGAA	4067
rs779254911	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55896240	ATGCCACTGCACTCC[A/T]GCCTGGGTAGCAGAG	4067
rs779255593	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55961822	CAAAAACTGGTGTGT[A/C]GACCTCTGAGAGGAA	4067
rs779255612	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55934071	TCTTTACTAAAAGTA[C/T]AAAAATTAGCCAGGC	4067
rs779278319	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55996055	TGGTGACAAGTTTGA[A/G]GGCTCCAATGTATAC	4067
rs779287185	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55977849	GATCGAACCCGGGAA[C/G]TTGAGGCTCAAGTGA	4067
rs779308504	snp	C/T			intron-variant	LYN	GRCh38.p7	8:56001401	CTGCTGAGATGCAAA[C/T]CAGGGAAGGCTTTTG	4067
rs779326145	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55900121	GACACTGAAAACCAG[C/T]CAGCAAGGCCAAAAC	4067
rs779340634	in-del	-/C			intron-variant	LYN	GRCh38.p7	8:55920483	CTTGCTCTGAGAGAG[-/C]ATTTAACATATGCTA	4067
rs779377797	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55929362	TGCTTTTCTCATAGA[A/T]AATCTCTGGATCTGT	4067
rs779430786	in-del	-/C			intron-variant	LYN	GRCh38.p7	8:55903768	CCTGTAATCCCAGCA[-/C]TATGGGAGGCCAAGG	4067
rs779431755	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55928320	CCGGCTAGTTTTTGT[A/G]TTTTTAGTAGAGATG	4067
rs779433514	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55911982	GAGCTCAATATCGTC[A/G]TGGTGTGTTCTACCA	4067
rs779445874	snp	A/C	0.000863931	0.0207658	utr-variant-5-prime, missense	LYN	GRCh38.p7	8:55879975	CCAGCAGCCCCTCGC[A/C]GCGCGTCCAGCGTTC	4067
rs779529301	snp	C/G	0.000779727	0.0197296	utr-variant-5-prime, missense	LYN	GRCh38.p7	8:55880101	AACTTTCACCGCGAG[C/G]GGGTGAGTCCTCTGC	4067
rs779541947	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55916653	TCCACAATGCCTCTC[C/T]CTCCTCCCCTGGGAG	4067
rs779606369	snp	A/G	6.58957e-05	0.00573964	missense	LYN	GRCh38.p7	8:55953925	CCTGGGAGATCCCCC[A/G]GGAGTCCATCAAGTT	4067
rs779616892	snp	A/G	1.7187e-05	0.00293142	intron-variant	LYN	GRCh38.p7	8:55953793	GGTAAAGTACAAAGT[A/G]TTGCATTTCTTAACC	4067
rs779634544	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55958475	AAAAATTGTGGTTAA[A/C]TACACGTGACATAAA	4067
rs779642445	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55957482	TCAGTAGCCCTGCAT[A/G]TAAAGTCATGGCTTG	4067
rs779682346	snp	A/G			upstream-variant-2KB, utr-variant-5-prime	LYN	GRCh38.p7	8:55879324	GCCATTTGACTCTAC[A/G]TCATCCCCTCCCCCA	4067
rs779702460	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55883521	ATACTGGCTGCTGTC[C/T]GAGCAGCCCTAGTGA	4067
rs779714676	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55984542	ATATCCAATTCCTCA[G/T]CAAGTCTGGGGTTCT	4067
rs779740200	snp	A/G	1.64955e-05	0.00287184	synonymous-codon	LYN	GRCh38.p7	8:56010083	TTTCTACACAGCCAC[A/G]GAAGGGCAATACCAG	4067
rs779763138	snp	A/G			intron-variant	LYN	GRCh38.p7	8:56004930	GCTAGGACTACAGGC[A/G]CATGCCACCACACCC	4067
rs779782976	in-del	-/GTGTATATATAT			intron-variant	LYN	GRCh38.p7	8:55911190	TATATATATATATAC[-/GTGTATATATAT]ACACACACATATATA	4067
rs779832821	snp	A/G			intron-variant	LYN	GRCh38.p7	8:56009051	GGCTGACTTAAGGGT[A/G]CTGACTTTAAGTAAA	4067
rs779832927	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55891849	ACCTACCAAGCAGAC[A/G]GGTGTTCACTTTTTT	4067
rs779883110	snp	A/G			intron-variant	LYN	GRCh38.p7	8:56002937	CAGAAATCGGTAAAC[A/G]TTGCCAAAATATGCC	4067
rs779890177	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55995778	GTGGAGGGCTGAGCC[A/G]GGGCCGGGTCATACG	4067
rs779902352	in-del	-/G			intron-variant	LYN	GRCh38.p7	8:55902598	TTCAATCAATATATA[-/G]CATACAAAAAAAAAA	4067
rs779954749	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55921087	TTTGTTTGTTTTCAT[C/T]GTCTAGATACGTCTG	4067
rs779983528	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55909500	CTTTATCTAGTCATC[C/T]GCTGATGGACATTTA	4067
rs780002435	snp	C/T	1.64912e-05	0.00287147	synonymous-codon	LYN	GRCh38.p7	8:55947716	GAGAAGATGAAAGTC[C/T]TGGAGGAGTAAGTGC	4067
rs780006870	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55935671	CCCCACTACTTGCTA[C/G]TCAGGAGGCTGAGGC	4067
rs780010280	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55906336	GAATTCGTTTTTTTT[G/T]TTTTGTTTTGTTTTG	4067
rs780021990	snp	C/T	1.66441e-05	0.00288474	synonymous-codon	LYN	GRCh38.p7	8:55966722	CTTCCTAGGTTACTA[C/T]AACAACAGTACCAAG	4067
rs780024801	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55969412	GGGAGGTGGCAGTGA[A/G]TGGATCATGGTGGCA	4067
rs780042942	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55882893	TCCACCTTTGGACTT[C/G]TAGTGTGTGCTCAAT	4067
rs780064603	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55892634	TGCAGCCTTGAACTC[C/T]TGGGCTCAAATGATC	4067
rs780079975	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55896398	TCTCAGCAAACTAAC[A/G]TAAGAACAGAAAACC	4067
rs780130542	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55991791	TGTGCTCAGTAAACC[A/G]CTTTTTAAAAACGAA	4067
rs780174591	snp	A/G			upstream-variant-2KB, missense	LYN	GRCh38.p7	8:55879768	ACTTCCCCGCCCTCC[A/G]GGCTCAATATGCAAA	4067
rs780205165	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55935083	CCCACACCATGGAGG[C/G]AGCTCTGTGATCTGA	4067
rs780246911	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55939081	TCAGTTTTTGTCAGG[A/T]GTATATTGTATTTTC	4067
rs780317609	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55943407	ATGGTGAAACCTCAG[C/T]TCTACTAAAAGTACA	4067
rs780321484	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55930766	GTCTTGCCTCTTCCT[C/G]CTCCCCCTGCTGGCT	4067
rs780352463	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55977676	CCAGCTCTTTGGGAG[A/G]CTGAAGTGGGAGGGT	4067
rs780366159	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55903245	TGATTCGCCCACCTC[A/G]GCCTCCCAAAGTGCT	4067
rs780375889	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55941281	CCTCCCTCTCTGGCC[C/T]TGACTCCTGACCTTC	4067
rs780385390	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55954268	TCATGATTCCCTCAT[C/T]GCCAGATTCTCTGGA	4067
rs780395088	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55898821	TAAATTTTAGGAAAC[C/T]GGTTTTAATGATTTC	4067
rs780402905	snp	A/G			intron-variant	LYN	GRCh38.p7	8:56007909	AGACGACTTCAGGTC[A/G]GGAGTTTGAGACCAG	4067
rs780403845	snp	C/T			utr-variant-3-prime, downstream-variant-500B	LYN	GRCh38.p7	8:56012053	CTTCTCCCAGTTCCT[C/T]CTCTTCTTGCCATTT	4067
rs780405582	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55967651	TATTCATTTTCCTTT[G/T]CAGCATTATCTAAGT	4067
rs780406416	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55999800	AACATGGAGAAACCC[C/T]GTCTCTACTAAAATT	4067
rs780420596	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55987624	TTTCACCACATTGGG[C/T]AGGCTGGTCTCGAAC	4067
rs780433460	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55927175	GACAAGTGTATAATG[A/G]CATGTATTCACCATT	4067
rs780473335	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55931075	GTCATATACATATAC[A/G]TGTGTGTATATATAT	4067
rs780484344	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55976906	TTAAGGAAACTAGGC[C/T]GAGCACAGTGGCTCA	4067
rs780486697	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55938187	TCACATTTTCTGGAT[A/G]GGTCAGTGGGTGTTG	4067
rs780495947	snp	A/G	1.65127e-05	0.00287334	intron-variant	LYN	GRCh38.p7	8:55999375	ATGACTTTTTTGTTT[A/G]AGTTTAAATACCCAA	4067
rs780496311	in-del	-/AAAAGAAAG			intron-variant	LYN	GRCh38.p7	8:55905414	ACTCCGTCTCAAAAA[-/AAAAGAAAG]AAAAGAAAGAAAGAA	4067
rs780589102	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55918062	CAAGGCTGCACTGAG[A/G]AGGAACCAGGGTGGT	4067
rs780605113	snp	A/G			intron-variant	LYN	GRCh38.p7	8:56001337	TAGCTGGGGGTTAGA[A/G]TGGCTCAGGGAGAGA	4067
rs780609334	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55910619	TGGACAAGATTGCTT[A/T]GGTATTTGTGCTCTC	4067
rs780632434	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55915521	ACCAGCCTGGTCAAC[A/G]TGGTGAAACCCCGTC	4067
rs780636925	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55949986	ATCTCTGAAGACTGA[A/C]CTATTCTGGATATTT	4067
rs780656483	snp	C/T			intron-variant, upstream-variant-2KB	LYN	GRCh38.p7	8:55922196	AGACACAAGCAATTC[C/T]CTCACCTCAGCCTCC	4067
rs780684552	snp	C/T			intron-variant	LYN	GRCh38.p7	8:56003660	GCCTGAGCTACAAAG[C/T]GAGACTCTGTCTCAA	4067
rs780704060	in-del	-/AAAT			intron-variant	LYN	GRCh38.p7	8:55954840	ACCCTGCCTCAAAAT[-/AAAT]AAATAAATAAATAAA	4067
rs780721504	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55967583	AGCCTCTGAAAGTGC[A/T]AGGATTACAGGCATG	4067
rs780737940	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55900587	GACCTTACTATGGTG[C/T]CCAGGCTAGTCTCAA	4067
rs780739981	snp	C/G	4.98716e-05	0.00499333	intron-variant	LYN	GRCh38.p7	8:55946408	TGTGAGTAAGAAAAG[C/G]TAAACAGAATTTTTT	4067
rs780743901	snp	C/T	1.65449e-05	0.00287614	synonymous-codon, intron-variant	LYN	GRCh38.p7	8:55941922	AGTAGATTTGAAGAC[C/T]CAACCAGTACGTAAT	4067
rs780761762	snp	C/G	1.64852e-05	0.00287094	synonymous-codon	LYN	GRCh38.p7	8:55998393	GAACTACATTCACCG[C/G]GACCTGCGAGCAGCT	4067
rs780765978	snp	A/T			intron-variant	LYN	GRCh38.p7	8:55966483	AGCAATTCTCCTGTC[A/T]CAGCATCCTGAGTAG	4067
rs780768427	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55938038	AAAAATTATCCCAGA[A/G]TCTGGGAATAAAATA	4067
rs780828965	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55944057	TCACGCCACTGCACT[C/T]CAGCCTGGGTTACAG	4067
rs780829040	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55956523	TTTAAATTTAGTTTC[G/T]CCGTGGCAACTTTTT	4067
rs780857424	in-del	-/TA			intron-variant	LYN	GRCh38.p7	8:55942421	ATATATATGTGTGTA[-/TA]TATATATATATGTGT	4067
rs780863027	in-del	-/A			downstream-variant-500B	LYN	GRCh38.p7	8:56012878	AGAGAAGGAAGGAGG[-/A]AAAAAAACGTGCCTT	4067
rs780866069	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55966651	GGGATTATAGGTGTG[A/G]GCCACCTCCCCCGGC	4067
rs780881925	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55955573	TAAAAGGAACAATCC[A/C]CTGGCATTTAGTACA	4067
rs780991001	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55995634	GCCAGGCATGGCTTC[C/T]GGGAGAAGTAAAATC	4067
rs781033368	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55898929	TTCTGGGCTCACGCA[A/G]TCCTCCTGCCTCAGC	4067
rs781037995	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55983460	CCTCTCCAGCTACCT[C/T]AGCCTCCAGGTGTCT	4067
rs781058645	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55991701	GCTTCAGGCACAGGC[A/G]TTTTCAGGAAACAAT	4067
rs781062725	snp	A/G			utr-variant-3-prime, downstream-variant-500B	LYN	GRCh38.p7	8:56012012	TATTTAAAGAAAATT[A/G]TTAAATTTATCTTCG	4067
rs781065555	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55906821	TAAGCCTCCAGATGA[A/G]GGAAGAAGGAGCAGC	4067
rs781076664	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55903129	TGGGATTACATGCGT[A/G]AGCCACTGCGCCCGG	4067
rs781087284	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55981405	TTGTTGGATGACTAT[A/G]CTGGCCACTTAAAAT	4067
rs781093303	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55930542	TAAATGGTCTATTTC[C/T]CTACCTTACGTAAGT	4067
rs781119923	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55958946	ACCTCTCTGAGACCT[C/T]ATTTTCCATTCCTTT	4067
rs781151044	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55990042	TCAGGAGTTTGAGAC[C/T]AGCCTGGCCAACATG	4067
rs781157348	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55916500	TGGTTCACAAAAGCA[A/G]TGAAGACATGTATCT	4067
rs781158897	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55971950	TGTGGATTCCAGGGG[G/T]CTTCAGTTGACTCTC	4067
rs781180632	snp	G/T			downstream-variant-500B	LYN	GRCh38.p7	8:56012583	AATTAGCTAAGTGTG[G/T]TGGCACATACCTATG	4067
rs781194878	snp	G/T			intron-variant	LYN	GRCh38.p7	8:55893049	GTACAAAGCCATTTG[G/T]TTTGGCAAATAAACA	4067
rs781194924	snp	C/G	1.70831e-05	0.00292254	intron-variant	LYN	GRCh38.p7	8:55966930	CCCAGAGCTTGCAAG[C/G]GCTTCAAACTCAAAA	4067
rs781284717	snp	C/T	3.30044e-05	0.00406216	intron-variant	LYN	GRCh38.p7	8:55947599	ATTCTTACAGGTGTT[C/T]TCTTGTGTTCATCTT	4067
rs781346549	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55929880	CTAGATCAGGCATCC[C/T]CAACCCCTGGGCCAT	4067
rs781350103	snp	C/T	1.65853e-05	0.00287964	utr-variant-3-prime	LYN	GRCh38.p7	8:56010125	GAGCACAGGGAGACC[C/T]GTCCATTTGGCAGGG	4067
rs781463762	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55940618	TGACCTCGTGATCCG[C/T]CTTCCTTGGCTTCAC	4067
rs781463890	snp	A/G/T	1.65007e-05	0.00287229	intron-variant	LYN	GRCh38.p7	8:55953991	TCTGGATGGGTAAGT[A/G/T]TGCGGCTCGGGGATC	4067
rs781467342	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55991975	AAACCTCACTGACAT[C/T]GTCTCTTTACGTGAT	4067
rs781473129	snp	A/C			intron-variant	LYN	GRCh38.p7	8:55902412	AGCTCACTGCAACTT[A/C]CGCCTCCCAGGTTCA	4067
rs781485898	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55987338	GCTCGAGCCCCGGAG[C/G]TGGAGGTTACAGTGA	4067
rs781496000	snp	A/G			utr-variant-3-prime	LYN	GRCh38.p7	8:56010974	GTTTGGAAGAACTAA[A/G]ATTCTAATCTCTGAA	4067
rs781506378	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55937202	TACCTCACAAGTGGA[C/G]TTTAGAACCTAACCA	4067
rs781521086	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55915753	AAATTCTCCTTACAT[A/G]TAAAACATATGAAGC	4067
rs781539680	in-del	-/TATG			intron-variant	LYN	GRCh38.p7	8:55942317	ATATATGTGTATATA[-/TATG]TGTATATATATGTGT	4067
rs781624002	in-del	-/A			intron-variant	LYN	GRCh38.p7	8:55952585	TACTAAAATAAAAGC[-/A]ATTAATTAATCTACA	4067
rs781630718	in-del	-/AGGAAATTATTTTTA	1.71076e-05	0.00292464	intron-variant	LYN	GRCh38.p7	8:55950823	TTTAAAACACTATTT[-/AGGAAATTATTTTTA]GAAACTATTCTAGAG	4067
rs781637423	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55936286	CTCTCTAATTCAGAA[A/G]ACTCATGGATCTGGA	4067
rs781639899	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55949170	ATAGTGTCCATCTCT[A/G]TGATAACTAGATGTT	4067
rs781643253	in-del	-/C			intron-variant	LYN	GRCh38.p7	8:55935799	AAAAAAAAAAAAAAA[-/C]AGGAATTTGGGAAAA	4067
rs781654715	in-del	-/CTCT			intron-variant	LYN	GRCh38.p7	8:55936271	TCATGTCTTTCTAAG[-/CTCT]CTAATTCAGAAAACT	4067
rs781659238	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55999042	GGCACATTGTCAGGG[A/G]GCCAAGCATGGTCGG	4067
rs781687744	snp	C/G			intron-variant	LYN	GRCh38.p7	8:55894184	CCCCAACCCCCCCAG[C/G]TTATTTTTATTTTAT	4067
rs781689319	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55881396	CAGCCAACACCTAAA[A/G]CCATGCCCTGGGGAA	4067
rs781740463	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55885176	TGCTCAGTGTTCAGA[A/G]TGCTGCTACTTAAAT	4067
rs781763302	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55907855	TGGGTGACAGAGTGA[A/G]ACCCTGTTTCACATA	4067
rs796089665	multinucleotide-polymorphism	ATG/GTC			downstream-variant-500B	LYN	GRCh38.p7	8:56012784	GCTCAGTCTTGAGAG[ATG/GTC]CCATTTGGTTTGACC	4067
rs796090393	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55954127	TTCCTCTGTCCATTG[A/G]GGCTGAGAACTGGCC	4067
rs796107162	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55962799	TGTTTATTTGCTTTA[C/T]GGTTCTTCAGATTTT	4067
rs796118792	snp	C/T			intron-variant	LYN	GRCh38.p7	8:56008073	GCAGTGAGCCAAGAT[C/T]GCTCCACTGCACTCC	4067
rs796177060	in-del	-/A			intron-variant	LYN	GRCh38.p7	8:55988950	CTTTGCCAATTTCTC[-/A]AAAAGCGATAGTAAT	4067
rs796201692	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55948229	TTCTCCTGCCTTGGC[C/T]TCCCAAAGTGCTGGG	4067
rs796204540	in-del	-/AAGAAAGC			intron-variant	LYN	GRCh38.p7	8:55976367	GGAAGGAAGGAAAGA[-/AAGAAAGC]AAGAAAGCATTTTGA	4067
rs796226180	snp	G/T			intron-variant	LYN	GRCh38.p7	8:56000281	GAAATAACCACCTTT[G/T]TTTATCAGTGGGAGG	4067
rs796254670	in-del	-/TA			intron-variant	LYN	GRCh38.p7	8:55911216	ATATATATACACGTG[-/TA]TATATATATACATAT	4067
rs796263389	in-del	-/TGA			utr-variant-3-prime, downstream-variant-500B	LYN	GRCh38.p7	8:56012182	AGTCACACGTTCCCT[-/TGA]TGAACAGCACACACA	4067
rs796266069	snp	C/T			upstream-variant-2KB	LYN	GRCh38.p7	8:55877008	ACTGCTTCTTAGGTT[C/T]CTGTGAGTCTCTGGA	4067
rs796288391	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55947076	AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAC	4067
rs796307940	in-del	-/A			intron-variant	LYN	GRCh38.p7	8:55919266	TATTGAAAAGAAGAG[-/A]AAAGAGTGGAGAGGG	4067
rs796337814	in-del	-/A			intron-variant	LYN	GRCh38.p7	8:55952399	CCCCATCTCTACTAG[-/A]AAAAAAAAAAATTAG	4067
rs796419375	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55961823	AAAAACTGGTGTGTC[A/G]ACCTCTGAGAGGAAA	4067
rs796425227	in-del	-/GTGT			intron-variant	LYN	GRCh38.p7	8:55909989	TGTGTGTGTGTGTGT[-/GTGT]CTTTTTTTTTTTTTT	4067
rs796427700	in-del	-/AG			intron-variant	LYN	GRCh38.p7	8:55976591	GTTGCAGGCAAAGAC[-/AG]GGTACAGCCCTGGGA	4067
rs796445992	in-del	-/G			intron-variant	LYN	GRCh38.p7	8:55917188	TAAAAAAAAAAAAAA[-/G]AGAGAGAGAGAGAGA	4067
rs796446717	in-del	-/T			intron-variant	LYN	GRCh38.p7	8:55959130	AGTTGTTATTTTCTG[-/T]TTTGGGGATTTTTTT	4067
rs796501463	in-del	-/AAC			intron-variant	LYN	GRCh38.p7	8:55897914	AGGCCCTGTCTCACA[-/AAC]AACAACAACAACAAC	4067
rs796578446	in-del	-/AGAG			intron-variant	LYN	GRCh38.p7	8:55939463	CCTTTTCCCAAGAGA[-/AGAG]AGAGAGAGAGAGAGA	4067
rs796699457	snp	A/G			intron-variant	LYN	GRCh38.p7	8:55885325	CTCAGATAGTTTTTT[A/G]GTTGGTCTCATTTCC	4067
rs796702706	in-del	-/T			intron-variant	LYN	GRCh38.p7	8:55894388	TAATTTTTTTTTTTT[-/T]GAGACAGTGGTCACT	4067
rs796777940	in-del	-/T			intron-variant	LYN	GRCh38.p7	8:55894375	GATTAACTTTCTTAA[-/T]TTTTTTTTTTTTTGA	4067
rs796795925	in-del	-/AG			intron-variant	LYN	GRCh38.p7	8:55956118	ATGCTCATTAAAAAA[-/AG]AATGACTTGGCTTCT	4067
rs796796715	in-del	-/ATAC			intron-variant	LYN	GRCh38.p7	8:55911180	TATACACGTATATAT[-/ATAC]ATATATATACACACA	4067
rs796838413	in-del	-/T			intron-variant	LYN	GRCh38.p7	8:55890745	TTTTTTTTTTTTTTT[-/T]GAAACAGGGTTTTAC	4067
rs796864641	in-del	-/TATTC			intron-variant	LYN	GRCh38.p7	8:55929130	TATTTCTGGGCTGTT[-/TATTC]TATTCATATGTACTG	4067
rs796891440	snp	C/T			intron-variant	LYN	GRCh38.p7	8:56009333	TGAATGCTGTCTTGA[C/T]CCCCTCCATGCTAAA	4067
rs796900279	in-del	-/AAT			intron-variant	LYN	GRCh38.p7	8:55954869	ATAAATAAATAAATA[-/AAT]AAAAGTTTTCATAGT	4067
rs796923826	snp	C/T			intron-variant	LYN	GRCh38.p7	8:55913046	TAGTGGGATGTCTGC[C/T]TGTTGAAACCATTTT	4067
rs796956253	in-del	-/T			intron-variant	LYN	GRCh38.p7	8:55898999	TGGGCTAATTTTTTT[-/T]ATTTTTTGTAAGGAT	4067

Page 1 | 2