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

MYLIP

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs12109	snp	G/T	0	0	missense, utr-variant-5-prime	MYLIP	GRCh38.p7	6:16129365	GCGGTGCTGATGGAG[G/T]TGGAGGTGGAGGCGA	29116
rs760632	snp	C/T	0.356383	0.226236	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128841	CACCAGCCGCCTCTG[C/T]CCGCTGGGCGACGCT	29116
rs760633	snp	C/G	0.442655	0.159323	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128734	CTCCAAGCTGCCACT[C/G]TTCTTCAAATATCTT	29116
rs909562	snp	C/T	0.390838	0.206555	intron-variant	MYLIP	GRCh38.p7	6:16130102	CTTCACAAGCGGTTT[C/T]CCAAACA	29116
rs1011616	snp	A/G	0.338523	0.233803	intron-variant	MYLIP	GRCh38.p7	6:16132178	TATTTGGTACTCCAA[A/G]CTTCTGAAGATTTAA	29116
rs1060901	snp	C/T	0.0486741	0.148216	synonymous-codon	MYLIP	GRCh38.p7	6:16145242	GTGCATGGTGTGCTG[C/T]GAGGAGGAGATCAAC	29116
rs1060913	snp	A/G	0.340108	0.233197	intron-variant	MYLIP	GRCh38.p7	6:16146509	TTCAACCTGTGAGAC[A/G]GCAAAGATCTCTACC	29116
rs1076632	snp	A/G	0.0770498	0.180522	intron-variant	MYLIP	GRCh38.p7	6:16129469	CCGAGGGGCCTCGCA[A/G]CGACGCCTGGCACTC	29116
rs2056937	snp	A/G	0.497182	0.037434	intron-variant	MYLIP	GRCh38.p7	6:16144383	TTAAAAAATCCTTCC[A/G]TACACAGTGACGACT	29116
rs2066905	snp	C/G	0.356169	0.226336	intron-variant	MYLIP	GRCh38.p7	6:16131066	TCAGGAAGTCAGTCA[C/G]TCGGGTAGGGTGGTT	29116
rs2072780	snp	A/G	0.373598	0.21731	intron-variant	MYLIP	GRCh38.p7	6:16144689	GACATTATGGCTTCC[A/G]TAAAGCAGTAAATAC	29116
rs2072781	snp	A/G	0.282632	0.247861	utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16147118	TAGGAAACTTACCTC[A/G]GGATACATTAAGGAG	29116
rs2072782	snp	G/T	0.00755907	0.0610114	intron-variant	MYLIP	GRCh38.p7	6:16146442	TGACATAGTATAAAC[G/T]GAAGGAAATTAATTA	29116
rs2072783	snp	C/T	0.283453	0.247752	intron-variant	MYLIP	GRCh38.p7	6:16143666	AAAAGAAAGCAGATC[C/T]AGAAGGAGTGATTCT	29116
rs2072784	snp	C/T	0.314057	0.241654	intron-variant	MYLIP	GRCh38.p7	6:16143633	ACCATGTGTGTGCCT[C/T]TGTGGGATCCCCATT	29116
rs2076017	snp	C/T	0.196771	0.244268	intron-variant	MYLIP	GRCh38.p7	6:16130328	CATGACCAATTGCAA[C/T]AGAGAAAAAAGGAGT	29116
rs2142674	snp	G/T	0.361263	0.223876	intron-variant	MYLIP	GRCh38.p7	6:16138434	AGAACTTCAGTGATG[G/T]CTCAATATTTATGGG	29116
rs2142675	snp	C/G	0.494442	0.0524218	intron-variant	MYLIP	GRCh38.p7	6:16138132	TTTCTCTGTCTTAAG[C/G]AAATGTCCATGAATA	29116
rs2205794	snp	C/T	0.123798	0.215808	utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16147945	AGCTAGTATTGCACC[C/T]GATAAGGTCATCTAG	29116
rs2205795	snp	A/C	0.340333	0.233109	utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16147827	CAAAAAGAACCAAAA[A/C]CCCTTCGAAACATAC	29116
rs2205796	snp	A/C	0.376791	0.215463	intron-variant	MYLIP	GRCh38.p7	6:16142766	TTGGAAGAATTATGG[A/C]AAGTCTCTAAAAATA	29116
rs2235215	snp	A/G	0.48546	0.0840147	intron-variant	MYLIP	GRCh38.p7	6:16130925	TTGGAAAATGCACTC[A/G]GACCAAGTAGGTAGC	29116
rs2237106	snp	A/G	0.287867	0.247116	intron-variant	MYLIP	GRCh38.p7	6:16133755	GTGGCTAAGTCGGGA[A/G]CAAAATATAGATTTT	29116
rs2237107	snp	C/G	0.301932	0.244547	intron-variant	MYLIP	GRCh38.p7	6:16133589	ATGATTATTATTTCA[C/G]ATCTACTTCCAGAAT	29116
rs2282813	snp	A/C	0.317933	0.240593	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140400	ATCCTGTTTAAGCCC[A/C]TCCTAGTTGTATACA	29116
rs2282814	snp	C/T			intron-variant	MYLIP	GRCh38.p7	6:16139439	TTGCCACAAACGAAG[C/T]CTTCTTAGTTTAATT	29116
rs2327950	snp	C/T	0	0	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128323	TTTCTTTTCTTTTTT[C/T]TTTTTTTTTTTTTTT	29116
rs3071239	in-del	-/TTTT			upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128342	ttttttttttttttt[-/TTTT]gagacagggtttttt	29116
rs3071241	in-del	-/T/TT			upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128512	tttgttttttttttt[-/T/TT]gtatttttagtagag	29116
rs3216216	in-del	-/T	0.495368	0.0478996	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140356	CATTTACTAAAAGGT[-/T]ATGTCACACTTAAAA	29116
rs3757352	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128640	AAAGAAAACTGTTCT[C/G]GTccgggcatggtgg	29116
rs3757353	snp	C/T	0.373598	0.21731	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16127642	GGTTTCGCAACACAG[C/T]GAAACCCCATCTCTA	29116
rs3757354	snp	A/G	0.440333	0.16209	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16127176	AAGGATCTGTTAGTG[A/G]CCTTTATTTCCGAAC	29116
rs3765234	snp	A/C	0.178785	0.239642	utr-variant-5-prime	MYLIP	GRCh38.p7	6:16129267	GTGTGCGCGGGGCTG[A/C]CGCCTTGTCACTGGT	29116
rs4515393	snp	A/G	0.0463947	0.145069	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140997	ATTTAAATAGTTTTC[A/G]GAGAGAAGAAAGTCA	29116
rs4716047	snp	A/G	0.361894	0.223562	intron-variant	MYLIP	GRCh38.p7	6:16138027	TTTCTTAGTAACTGG[A/G]TAAAACTTAAAGAAG	29116
rs4716048	snp	C/G	0.487933	0.0767327	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140596	GGTATCCAAGCAAGG[C/G]GACAGAAAGAATGGC	29116
rs4716049	snp	A/T	0.486855	0.0799975	downstream-variant-500B, intron-variant	MYLIP	GRCh38.p7	6:16148512	GGAGATCACTTCACC[A/T]GGTTATTCTCTTATT	29116
rs4716050	snp	A/G	0.484138	0.0876334	downstream-variant-500B, intron-variant	MYLIP	GRCh38.p7	6:16148513	GAGATCACTTCACCA[A/G]GTTATTCTCTTATTT	29116
rs5874546	in-del	-/T			upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128317	TTTCTTTTTCTTTTC[-/T]TTTTTTTTTTTTTTT	29116
rs6920309	snp	C/T	0.35207	0.228214	intron-variant	MYLIP	GRCh38.p7	6:16134016	CTTTCTGACCTCAGC[C/T]CCATCCTCAGCCCTC	29116
rs7738525	snp	A/G	0.486464	0.0811471	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16141371	ATTTTATGTTTTGTA[A/G]CCTTAATGTTACCGA	29116
rs7756075	snp	A/G	0.258565	0.249853	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16141385	AACCTTAATGTTACC[A/G]AACTTGTGTTAAATA	29116
rs7763395	snp	A/G	0.491263	0.0655142	intron-variant	MYLIP	GRCh38.p7	6:16142128	CATCAGGGCTACTGC[A/G]TATATTCATAGAGCT	29116
rs8180638	snp	C/T	0.382085	0.212258	intron-variant	MYLIP	GRCh38.p7	6:16134945	GGAAGGTTTTTAAAA[C/T]GACATGTAAAATTAA	29116
rs9297003	snp	C/T			intron-variant	MYLIP	GRCh38.p7	6:16135805	attctatatagtgta[C/T]atatacagtatatat	29116
rs9297004	snp	C/G	0.029116	0.117091	intron-variant	MYLIP	GRCh38.p7	6:16135813	tagtgtatatataca[C/G]tatatattctatata	29116
rs9349995	snp	A/T	0.297128	0.245518	intron-variant	MYLIP	GRCh38.p7	6:16134371	GAAAAGTTGAGAGTA[A/T]CTAAAAGAAATCTCA	29116
rs9370867	snp	A/G	0.47729	0.104112	missense	MYLIP	GRCh38.p7	6:16145094	ACCTCGTTTCAAGAA[A/G]CAACCAGAGCCCTTC	29116
rs9396644	snp	C/T	0.0399052	0.1355	intron-variant	MYLIP	GRCh38.p7	6:16145537	CTCCAAATTATGCAG[C/T]GTTTTCAAGTTCTGA	29116
rs10602844	in-del	-/TATATA			intron-variant	MYLIP	GRCh38.p7	6:16135756	GTGTATACATATATC[-/TATATA]TATATATATATATAT	29116
rs11354447	in-del	-/A	0.493201	0.0579089	intron-variant	MYLIP	GRCh38.p7	6:16137887	TATATTCACTCCATT[-/A]AAAAAAAAATCTATA	29116
rs11394742	in-del	-/AA			intron-variant	MYLIP	GRCh38.p7	6:16131047	AAAAAAAAAAAAAAA[-/AA]GAAACCACCCTACCC	29116
rs11552211	snp	A/G			utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16148131	TAAATACCTCTTGGA[A/G]TAAAGGCTTATATGC	29116
rs11963978	snp	C/T	0.00597247	0.0543191	downstream-variant-500B, intron-variant	MYLIP	GRCh38.p7	6:16148328	ACATCACAGTTAGTA[C/T]CTACTTTCCTCCTAC	29116
rs11968699	snp	A/G	0.0150606	0.0854603	intron-variant	MYLIP	GRCh38.p7	6:16138327	CTACTTTACAAAAAA[A/G]AAAAGGAGGGGGCAA	29116
rs11969716	snp	A/G	0.00199481	0.0315187	intron-variant	MYLIP	GRCh38.p7	6:16142861	TCTTAGACGTTTTTT[A/G]TAGTAAGTTCGCTAA	29116
rs12202423	snp	G/T			utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16147933	ATGTCGGGAGACCTA[G/T]ATGACCTTATCGGGT	29116
rs13192810	snp	A/T			intron-variant	MYLIP	GRCh38.p7	6:16129511	CTACTAGGGGCCGGG[A/T]GGCACTGCGGCGGCA	29116
rs13194722	snp	G/T			upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128523	tttttgtatttttag[G/T]agagacgggggtttc	29116
rs13206355	snp	A/G			intron-variant	MYLIP	GRCh38.p7	6:16129512	TACTAGGGGCCGGGA[A/G]GCACTGCGGCGGCAG	29116
rs13207341	snp	A/C			intron-variant	MYLIP	GRCh38.p7	6:16129499	CTGGCGCGCCCCCTA[A/C]TAGGGGCCGGGAGGC	29116
rs34308252	in-del	-/C			intron-variant	MYLIP	GRCh38.p7	6:16131903	TGAGTTCTTGGTACT[-/C]CCTGAAAATATCTTG	29116
rs34444721	snp	A/G	0.000723251	0.0190027	intron-variant, nc-transcript-variant	MYLIP, MIR4639	GRCh38.p7	6:16141594	GTCAGGTTATCCCCA[A/G]GCATAACCTCACTCT	29116
rs34627146	snp	A/G	0.0113489	0.0744692	synonymous-codon, intron-variant	MYLIP	GRCh38.p7	6:16143849	AGCGATAACAGAGAC[A/G]CACGCATTCTACAGG	29116
rs34659321	in-del	-/G			intron-variant	MYLIP	GRCh38.p7	6:16129836	CAGTCTCGGGCCCCA[-/G]GGGTTCTTGGCAGAC	29116
rs34983380	in-del	-/G			upstream-variant-2KB	MYLIP	GRCh38.p7	6:16127633	ATTTTGTGTAGAGAT[-/G]GGGGTTTCGCTGTGT	29116
rs35112615	in-del	-/A/AA			utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16146867	TAAAAAAAAAAAAAA[-/A/AA]GGAAGAAAAATAACA	29116
rs35212780	snp	A/C	0.027392	0.113779	synonymous-codon	MYLIP	GRCh38.p7	6:16143170	GCTCATTGGGGTTGG[A/C]CCTGAAGGAATCTCA	29116
rs35613901	in-del	-/G			intron-variant	MYLIP	GRCh38.p7	6:16134718	CACAAAATAGGCCCT[-/G]GGAAAGTAAAAACAG	29116
rs35729822	snp	A/G			intron-variant	MYLIP	GRCh38.p7	6:16132736	ATGCATGAAACTATA[A/G]AACAAAAATATGTAT	29116
rs35731512	in-del	-/G			intron-variant	MYLIP	GRCh38.p7	6:16142603	TGAAGGCTCGACTGA[-/G]GGGTGGCCTCCATGC	29116
rs36160962	snp	C/T			upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128288	AGTTTTCTTTTTCTC[C/T]TTTTTTTTTCTTTTT	29116
rs45542142	snp	A/G	0.0158469	0.0875917	intron-variant	MYLIP	GRCh38.p7	6:16144727	GTTAGAGAAACAGAG[A/G]TGTAATCACTGAGAA	29116
rs55828581	snp	A/G	0.0166325	0.0896639	intron-variant	MYLIP	GRCh38.p7	6:16139475	TTCAAGTCTTTCAGA[A/G]CGTAATTTCTTCTTT	29116
rs56215044	snp	A/C			intron-variant	MYLIP	GRCh38.p7	6:16135755	TGTGTATACATATAT[A/C]TATATATATATATAT	29116
rs57547267	snp	A/G			intron-variant	MYLIP	GRCh38.p7	6:16135779	TATATATATATATAT[A/G]TATGCTATATATTCT	29116
rs61711295	in-del	-/AAG			intron-variant	MYLIP	GRCh38.p7	6:16143294	ATAGAAAATAGGAAG[-/AAG]GGATTTACTCGACAG	29116
rs62387664	snp	A/G	0.5	0	utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16146883	AAAAAAAAAAAAAAG[A/G]AAGAAAAATAACACA	29116
rs71716432	in-del	-/T/TT	0.280785	0.248097	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128501	CGCCTGGCTATTTTG[-/T/TT]TTTTTTTTTTTGTAT	29116
rs72833422	snp	G/T	0.0146672	0.084371	intron-variant	MYLIP	GRCh38.p7	6:16133501	GCATATTTCAGAGAT[G/T]GAGACAGCAGGTTAT	29116
rs72833427	snp	A/C/T	3.29453e-05	0.00405854	synonymous-codon	MYLIP	GRCh38.p7	6:16145071	TCTGTACAATGCTGG[A/C/T]GTTGTGGACCTCGTT	29116
rs73377721	snp	C/T	0.0107246	0.0724382	intron-variant	MYLIP	GRCh38.p7	6:16131556	GAGACTTCAATCTTA[C/T]AGTGGCATATCAAAA	29116
rs73724995	snp	A/G	0.0146672	0.084371	utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16147622	CAACTGAGGGTAGTT[A/G]ACTCATCACTTCTCC	29116
rs74484260	snp	A/G	0.0150606	0.0854603	intron-variant	MYLIP	GRCh38.p7	6:16144791	TTCATACATGCAGAC[A/G]AGACTATGAAACATC	29116
rs74519493	snp	A/G	0.00755907	0.0610114	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140852	AGAAATGACAAGTTT[A/G]TACTAGAAACAAGCA	29116
rs74641795	snp	C/T	0.0287284	0.116357	downstream-variant-500B, intron-variant	MYLIP	GRCh38.p7	6:16148453	ATAGTCTTTTTTTTT[C/T]TTTTTCAAGAAAACT	29116
rs74708826	snp	A/G	0.5	0	utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16146881	TTAAAAAAAAAAAAA[A/G]GGAAGAAAAATAACA	29116
rs75833122	snp	G/T	0.0162398	0.0886349	intron-variant	MYLIP	GRCh38.p7	6:16146435	AAAAATGTAATTAAT[G/T]TCCTTCAGTTTATAC	29116
rs76272508	snp	A/G	0.0189856	0.0955633	intron-variant	MYLIP	GRCh38.p7	6:16144003	GAACATTTTGTTTCC[A/G]TAGTAGCAGTGGAGT	29116
rs76482829	snp	C/T	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140073	CTTGCTCATGTTCCT[C/T]TACCTGGAATGTCAG	29116
rs76502194	snp	G/T	0.5	0	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128513	TTTGTTTTTTTTTTT[G/T]TATTTTTAGTAGAGA	29116
rs76514709	snp	A/G	0.00159617	0.0282053	intron-variant	MYLIP	GRCh38.p7	6:16136385	CACAGATTTTTTGAG[A/G]TCCATCCATATTGTC	29116
rs76726799	snp	A/G	0	0	intron-variant	MYLIP	GRCh38.p7	6:16131032	GTGCTACCCCAGGAA[A/G]AAAAAAAAAAAAAAA	29116
rs77545634	snp	G/T	0	0	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128512	TTTTGTTTTTTTTTT[G/T]GTATTTTTAGTAGAG	29116
rs77832768	snp	C/T	0.0391387	0.134304	intron-variant	MYLIP	GRCh38.p7	6:16146204	TGGAGCTGCCACCTA[C/T]GGCTAGAAGCAGAGC	29116
rs77893654	in-del	-/TGG			cds-indel, intron-variant	MYLIP	GRCh38.p7	6:16147744	GTCCTTTTCTGTTTT[-/TGG]GGGGGGAGTTTTGTT	29116
rs78236759	snp	G/T	0.0107246	0.0724382	intron-variant	MYLIP	GRCh38.p7	6:16131553	CAGGAGACTTCAATC[G/T]TACAGTGGCATATCA	29116
rs78468965	in-del	-/AA			intron-variant	MYLIP	GRCh38.p7	6:16138330	CTTTACAAAAAAAAA[-/AA]GGAGGGGGCAAAACC	29116
rs78823578	snp	C/T	0.00755907	0.0610114	intron-variant	MYLIP	GRCh38.p7	6:16130453	GGAATTGTAACACCA[C/T]TGAACTTTGTAAAAA	29116
rs78892829	snp	C/G	0.5	0	intron-variant	MYLIP	GRCh38.p7	6:16139220	ATCCTGGCTAACACG[C/G]TGAAACCCCGTCTCT	29116
rs78931304	snp	G/T	0.5	0	intron-variant	MYLIP	GRCh38.p7	6:16136631	TGGAGTAAGTAATCA[G/T]TTCATTTTATAACTA	29116
rs79499663	snp	C/T	0.0146672	0.084371	intron-variant	MYLIP	GRCh38.p7	6:16138755	GTTGCTTTATAGCCA[C/T]GAAACTGCAAAATGC	29116
rs79693990	snp	A/T			upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128368	GGTTTTTTGCTCTTC[A/T]TGCCCAAGCTACAGT	29116
rs79714658	snp	C/T	0.00716266	0.059414	utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16147438	ACCCCACAAGCCTTT[C/T]GATTATAAAATACTA	29116
rs79871226	snp	C/T	0.142272	0.225598	intron-variant	MYLIP	GRCh38.p7	6:16134606	TTTAACTGCAACCCA[C/T]TTATAGTCCTAAGTA	29116
rs79992066	snp	A/C	0.0293239	0.117482	missense	MYLIP	GRCh38.p7	6:16143159	GGGCAGAAACTGCTC[A/C]TTGGGGTTGGACCTG	29116
rs80300728	snp	C/T	0	0	downstream-variant-500B, intron-variant	MYLIP	GRCh38.p7	6:16148445	TTGAGAGTATAGTCT[C/T]TTTTTTTTTTTTTCA	29116
rs80336179	snp	G/T	0.00795532	0.062565	intron-variant	MYLIP	GRCh38.p7	6:16132691	TCAGAAGCTGTACTG[G/T]GTCCAGTTTACAATT	29116
rs111481145	snp	A/T	0.5	0	intron-variant	MYLIP	GRCh38.p7	6:16130215	GCCAAAAATCAGCTG[A/T]GCAGAGTATGCTGGT	29116
rs111591442	in-del	-/A	0.5	0	intron-variant	MYLIP	GRCh38.p7	6:16139387	GCAAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA	29116
rs111679441	snp	C/T	0.5	0	intron-variant	MYLIP	GRCh38.p7	6:16144089	AAACACATTCTCTGC[C/T]TACCTCCTACCGTAT	29116
rs111682559	snp	A/G	0.5	0	intron-variant	MYLIP	GRCh38.p7	6:16130400	TCGTGGTTTGGTATC[A/G]TTGGAGCCGTGGAAC	29116
rs111886582	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16146590	GCACTAGAGACCAGG[A/G]GTGTGCACAGAGACA	29116
rs111924435	snp	C/T	0.5	0	intron-variant	MYLIP	GRCh38.p7	6:16143513	TCCCATACTTCCCTC[C/T]ACATATGCCCAACTG	29116
rs112375157	snp	C/G	0.0134861	0.0810011	utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16148155	GTATTTATTTTTTCA[C/G]TTGTAAAAAAATAAT	29116
rs112457725	in-del	-/G	0.0185938	0.0946107	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128500	ACGCCTGGCTATTTT[-/G]GTTTTTTTTTTTGTA	29116
rs112531050	snp	A/G/T	0.000543509	0.0164764	synonymous-codon, intron-variant	MYLIP	GRCh38.p7	6:16143756	GAATGTATATTTGAC[A/G/T]GTCACCAAGGAATCT	29116
rs112586731	snp	A/G	0.5	0	intron-variant	MYLIP	GRCh38.p7	6:16144332	GGAGAAGGATAGCAC[A/G]GATCATCTTTTCTTT	29116
rs112627470	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16141346	ATAATGCAGAAACTT[A/G]TGTGTAATTATTTTA	29116
rs112638243	snp	A/G			upstream-variant-2KB	MYLIP	GRCh38.p7	6:16127429	CTTTTTTTTTCTTTC[A/G]TTGTTTTCTTTTTGT	29116
rs112741245	snp	A/G	0.0777841	0.181223	intron-variant	MYLIP	GRCh38.p7	6:16132022	ATTTGTGAAAGCTTT[A/G]CGCTTCACTGTCATA	29116
rs112824443	snp	A/G	0.5	0	missense, intron-variant	MYLIP	GRCh38.p7	6:16143757	AATGTATATTTGACG[A/G]TCACCAAGGAATCTG	29116
rs112847490	snp	A/G	0.5	0	downstream-variant-500B, intron-variant	MYLIP	GRCh38.p7	6:16148376	TTTTTTAATAATTTC[A/G]GTGCTCTACAAATTC	29116
rs113021568	snp	A/G	0.000413131	0.0143664	synonymous-codon	MYLIP	GRCh38.p7	6:16145188	CCAGCAGACCCGGGT[A/G]CTGCAGGAGAAGCTA	29116
rs113117363	snp	G/T	0.000798403	0.0199641	utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16146971	ACCAGGAGGAGCTCT[G/T]GGACGCAGACACATT	29116
rs113193386	snp	A/G	0.5	0	missense	MYLIP	GRCh38.p7	6:16145282	TGTCCCTGTGGCCAC[A/G]CTGTGTGCTGTGAGA	29116
rs113232913	snp	G/T	0.5	0	utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16148170	CTTGTAAAAAAATAA[G/T]GTTTCCACGTAAAGA	29116
rs113692428	snp	A/T	0.0023933	0.0345097	intron-variant	MYLIP	GRCh38.p7	6:16144247	TTTACTTAGTCTAGG[A/T]CTCAGCTTCAAAGCC	29116
rs113830164	snp	G/T	0.5	0	intron-variant	MYLIP	GRCh38.p7	6:16138205	GATGTAGCCTCTATT[G/T]AATTGAATATGTCAT	29116
rs114004922	snp	A/G	0.0154538	0.0865337	utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16147609	GCCTCATGGTGTACA[A/G]CTGAGGGTAGTTAAC	29116
rs114100266	snp	G/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16146594	TAGAGACCAGGGGTG[G/T]GCACAGAGACACAGG	29116
rs114660342	snp	A/G	0.0115144	0.0749975	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140264	ACTTGTTATAACTGA[A/G]GCCAATCTGTCTACA	29116
rs114680787	snp	C/T	0.0463947	0.145069	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140479	TGTACATTTTTGGAG[C/T]TCTCTGATGTTCGAG	29116
rs115104829	snp	C/T	0.00318978	0.0398085	intron-variant	MYLIP	GRCh38.p7	6:16131780	GGACTGATAAAGACT[C/T]ATTTTGAAATACTTA	29116
rs115277586	snp	A/G	0.0130921	0.0798413	intron-variant	MYLIP	GRCh38.p7	6:16135470	AGTGATTCTCATTTT[A/G]TACTTTGGGCTTTGA	29116
rs115356871	snp	A/C	0.00993419	0.0697739	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140187	AATGTGGCAATTAGC[A/C]TTGTTTGAGAGGTTA	29116
rs115400722	snp	C/T	0.0130921	0.0798413	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128066	AGAGAGGGCCTGGTA[C/T]CCTGTAAGGCGTTTT	29116
rs115554968	snp	C/T	0.0126979	0.078662	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16139966	TAGTGAAAATAAGAT[C/T]AATGGCTCTTGTCAG	29116
rs116274408	snp	G/T	0.00597247	0.0543191	intron-variant	MYLIP	GRCh38.p7	6:16135331	TTTTTTAGAAGTGCA[G/T]ATTTTCTGCTTTCAA	29116
rs116277049	snp	C/G	0.0130921	0.0798413	intron-variant	MYLIP	GRCh38.p7	6:16130862	GATGCGGAGTTCCAT[C/G]TTAACTTAGGTTTTC	29116
rs116367169	snp	A/G	0.0205511	0.0992634	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16139574	GGTACATTCACCAAG[A/G]TGAAGTTTATCAAAT	29116
rs116454818	snp	A/C	0.00478085	0.0486577	intron-variant	MYLIP	GRCh38.p7	6:16136480	TGTTTATCCGTACTC[A/C]TAATAATGAACACCT	29116
rs116530625	snp	G/T	0.0142736	0.0832652	intron-variant	MYLIP	GRCh38.p7	6:16145551	GTGTTTTCAAGTTCT[G/T]AAAATGAGGCTGAGA	29116
rs116634947	snp	A/G/T	0.00993419	0.0697739	utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16147923	GTTTTCTGGGATGTC[A/G/T]GGAGACCTAGATGAC	29116
rs116670363	snp	A/G	0.0256215	0.110247	intron-variant	MYLIP	GRCh38.p7	6:16144840	TATTGACAACAGCGA[A/G]TAAGGGTGCTGCCAG	29116
rs117013782	snp	C/T	0.039522	0.134904	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16141384	TAACCTTAATGTTAC[C/T]GAACTTGTGTTAAAT	29116
rs117271482	snp	A/G	0.0232847	0.105357	intron-variant	MYLIP	GRCh38.p7	6:16138263	TTCACTGCAGGCATA[A/G]CTTATTTGACCACAT	29116
rs117833494	snp	A/T	0.0221141	0.102801	intron-variant	MYLIP	GRCh38.p7	6:16143619	CTAGGTCATGAGCAA[A/T]TGGGGATCCCACAAA	29116
rs117865383	snp	C/G	0.0240643	0.107019	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140881	CAGCATGGAAGGTAG[C/G]CTGCCTGCATGGAGT	29116
rs137908932	snp	A/C	0.00119737	0.0244387	intron-variant	MYLIP	GRCh38.p7	6:16131093	CTGATAGCAGCATCT[A/C]ATGCCCGATAGTAAC	29116
rs138175799	snp	C/T	6.58935e-05	0.00573955	missense, intron-variant	MYLIP	GRCh38.p7	6:16143755	AGAATGTATATTTGA[C/T]GGTCACCAAGGAATC	29116
rs138189082	snp	C/T	0.000106249	0.00728789	intron-variant, downstream-variant-500B	MYLIP, MIR4639	GRCh38.p7	6:16141836	TGAATATAGTATTGT[C/T]TACAACTAGAATAGG	29116
rs138217144	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16144494	TAAGAAATTTAAGTC[A/G]TAGACAACTTTAAAC	29116
rs138354667	snp	A/G	0.0209421	0.100162	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140653	CAGAGACACCAGAGC[A/G]TGAACATGCTTCCTA	29116
rs138482930	in-del	-/G			intron-variant	MYLIP	GRCh38.p7	6:16131049	AAAAAAAAAAAAAAA[-/G]AAACCACCCTACCCG	29116
rs138605319	snp	C/T			upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128775	ACCGTAAATTCGAGA[C/T]GGCAGAAAGGCGTCC	29116
rs138615948	snp	G/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16146320	GTCTCCTGCATTGCT[G/T]CCTGAAGTGTTATAG	29116
rs138820906	snp	A/G	0.000126518	0.00795255	synonymous-codon, intron-variant	MYLIP	GRCh38.p7	6:16146718	CGTCTATCTGCCAAC[A/G]CACACCAGTCTTCTC	29116
rs139020457	in-del	-/GAA	0.0452528	0.143452	intron-variant	MYLIP	GRCh38.p7	6:16143290	TGTAATAGAAAATAG[-/GAA]GAAGGGATTTACTCG	29116
rs139029844	snp	A/C	0.000214127	0.0103449	missense	MYLIP	GRCh38.p7	6:16144987	GAATGAAAACATTAA[A/C]CTTGGCAAGAAATAT	29116
rs139469255	snp	A/G	0.00146762	0.0270491	synonymous-codon, downstream-variant-500B, utr-variant-5-prime	MYLIP, MIR4639	GRCh38.p7	6:16141688	CTTGTGTTCCCCAGA[A/G]CAGGCAGTGGAACTC	29116
rs139533286	snp	C/G	0.0014675	0.0270481	missense, utr-variant-5-prime	MYLIP	GRCh38.p7	6:16129378	AGGTGGAGGTGGAGG[C/G]GAAAGCCAACGGCGA	29116
rs139611898	snp	A/C	0.00517822	0.0506191	intron-variant	MYLIP	GRCh38.p7	6:16132559	TAACTTGCTTTTAAT[A/C]TGTTGGTGAATTTTA	29116
rs139710389	snp	C/T	0.000798403	0.0199641	intron-variant	MYLIP	GRCh38.p7	6:16137083	CTATGTCCTGAGAAA[C/T]CTTTGCTACCTGGAA	29116
rs139714791	snp	G/T	0.00119737	0.0244387	intron-variant	MYLIP	GRCh38.p7	6:16142534	GGCCATGTCTTGGCT[G/T]GGTCCTCTGGCTCAT	29116
rs139744710	snp	C/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16143276	ATCTGTAGCTGTCAA[C/T]GTAATAGAAAATAGG	29116
rs139952026	snp	C/T	0.00597247	0.0543191	intron-variant	MYLIP	GRCh38.p7	6:16137907	AAAAATCTATAATGC[C/T]CAGTAAATGTTAATT	29116
rs140483917	snp	C/T	1.64917e-05	0.00287151	synonymous-codon, intron-variant	MYLIP	GRCh38.p7	6:16143708	TCTTAGGATAGCTTA[C/T]CCTGTGGTGCAGATG	29116
rs140662942	snp	C/T	0.00159617	0.0282053	intron-variant	MYLIP	GRCh38.p7	6:16135547	TGGCTGTGACAAGTT[C/T]CTCAGTGGCAAGCCC	29116
rs140682740	snp	C/T	0.0138799	0.0821421	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140129	CAGTGCTGAGGACAT[C/T]GCACCTGGCCAAAGT	29116
rs140760990	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140445	AAGGTAAACTAATCA[C/T]ACATAATATGCAGTT	29116
rs140825012	snp	A/G	0.00358779	0.0422022	intron-variant	MYLIP	GRCh38.p7	6:16133042	AGCCAAGTTGGGAAG[A/G]GCAGTTAACTTATTA	29116
rs141082770	snp	C/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16134163	TATTATCAGTCACTC[C/T]AATAACCTAAACTCC	29116
rs141183183	snp	C/T	0.000148737	0.00862243	missense	MYLIP	GRCh38.p7	6:16145183	AGCTGCCAGCAGACC[C/T]GGGTGCTGCAGGAGA	29116
rs141194819	snp	A/G	2.0905e-05	0.00323296	missense, intron-variant	MYLIP	GRCh38.p7	6:16146686	GTCTGCAGGTCGCGT[A/G]TGGAGCATGTCCAGC	29116
rs141302722	snp	C/G	0.00716266	0.059414	intron-variant	MYLIP	GRCh38.p7	6:16136904	TTTTATTTTTGAGTT[C/G]TACAAATTCTTCATG	29116
rs141559538	snp	C/T	0.000153988	0.00877328	missense, intron-variant	MYLIP	GRCh38.p7	6:16146732	CGCACACCAGTCTTC[C/T]CAATCTGACTGTAAT	29116
rs141584616	snp	C/T	0.00597247	0.0543191	intron-variant	MYLIP	GRCh38.p7	6:16133805	GTCTTTGCTAGGAGA[C/T]GTTTTGCTTAGGTAA	29116
rs141593682	snp	A/G	0.0023933	0.0345097	intron-variant	MYLIP	GRCh38.p7	6:16130478	TAAAAAGCACCAGCA[A/G]TCTTAGCCTCAGGGA	29116
rs141859471	snp	C/T	0.0111196	0.0737302	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16127528	AGCACACTGCAGCCT[C/T]GAACTCCCAGGCTCA	29116
rs141871032	snp	A/G	0.00398564	0.0444627	intron-variant, downstream-variant-500B	MYLIP, MIR4639	GRCh38.p7	6:16141997	TACTGTACCAGAGGA[A/G]TAGAGGATTTGCATG	29116
rs141980944	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16147936	TCGGGAGACCTAGAT[G/T]ACCTTATCGGGTGCA	29116
rs142124143	snp	A/G	0.0019255	0.0309684	missense	MYLIP	GRCh38.p7	6:16145084	GGCGTTGTGGACCTC[A/G]TTTCAAGAAACAACC	29116
rs142137048	snp	C/T	0.0142736	0.0832652	intron-variant	MYLIP	GRCh38.p7	6:16144054	TTTACCCACAGAAGG[C/T]GCATGTGTGTGAGCT	29116
rs142237330	snp	G/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16144841	ATTGACAACAGCGAA[G/T]AAGGGTGCTGCCAGG	29116
rs142405173	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16127126	GAGGATCCCTCCTTT[C/T]TTTTTAGCCTTGGGC	29116
rs142482330	snp	A/G	0.00159617	0.0282053	intron-variant	MYLIP	GRCh38.p7	6:16139444	AACTAAGAAGACTTC[A/G]TTTGTGGCAATATTC	29116
rs142596337	in-del	-/T	0.046775	0.145601	utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16146999	TTCCTTGGATGTTGA[-/T]TTTTTTTTATGATCT	29116
rs142778822	snp	A/G	0.00318978	0.0398085	intron-variant	MYLIP	GRCh38.p7	6:16133855	TCTCTTTTCCAGAAA[A/G]CAACCCCATTCCAAG	29116
rs143013423	snp	A/G	0.00636936	0.0560724	intron-variant	MYLIP	GRCh38.p7	6:16136775	TGGTAGAGTGTTGTG[A/G]TTTTAATTTGCATTT	29116
rs143150611	snp	C/G	1.64754e-05	0.00287009	missense	MYLIP	GRCh38.p7	6:16143200	AATTTGTAAAGATGA[C/G]TTTAGCCCAATTAAT	29116
rs143330356	snp	C/T	0.0130921	0.0798413	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128289	GTTTTCTTTTTCTCT[C/T]TTTTTTTTCTTTTTT	29116
rs143570847	snp	C/T	0.00914312	0.0669923	intron-variant	MYLIP	GRCh38.p7	6:16142802	CACCCATCCAGCATC[C/T]CCAAAGTGTTTTTAC	29116
rs143616256	snp	A/G	0.00318978	0.0398085	intron-variant	MYLIP	GRCh38.p7	6:16137261	TGATAGCTTTTAAAT[A/G]TAACTTGGCAGTCAA	29116
rs143656216	snp	C/T	0.0126979	0.078662	intron-variant, downstream-variant-500B	MYLIP, MIR4639	GRCh38.p7	6:16141890	TGGAAGGTAAACTAA[C/T]CACACATAATATGCA	29116
rs143704444	snp	C/T	0.000124152	0.00787785	synonymous-codon	MYLIP	GRCh38.p7	6:16145305	CTGTGAGAGCTGCGC[C/T]GCCCAGCTACAGGTA	29116
rs144304196	snp	C/G	0.00478085	0.0486577	utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16147378	GTAAAAAGCAGCTCA[C/G]TCAATGTGGGTGGCT	29116
rs144420622	snp	C/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16143480	CTAGACATGCATGTG[C/T]GCACACCCAGCACTT	29116
rs144460760	snp	G/T	0.00199481	0.0315187	utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16148191	CACGTAAAGAACTCT[G/T]TTATATCCTAGAGGA	29116
rs144531349	snp	A/G	0.00597247	0.0543191	intron-variant	MYLIP	GRCh38.p7	6:16132966	ACTGAAAGTATCTAG[A/G]CAGTTTATTAAATGA	29116
rs144630745	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16127199	AGATCCTTGGGACTC[A/G]TGAAGGGGGGTAGGG	29116
rs144669070	snp	G/T	0.00636936	0.0560724	intron-variant	MYLIP	GRCh38.p7	6:16133629	TCTTGCCTTTCAAAG[G/T]CTTTGAGTTTACTGC	29116
rs145017950	snp	C/T	2.1002e-05	0.00324046	missense, intron-variant	MYLIP	GRCh38.p7	6:16146717	ACGTCTATCTGCCAA[C/T]GCACACCAGTCTTCT	29116
rs145057345	snp	A/G	8.27055e-05	0.00643008	missense	MYLIP	GRCh38.p7	6:16145205	TGCAGGAGAAGCTAC[A/G]CAAGCTGAAGGAAGC	29116
rs145159643	snp	C/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16139032	GGAAGTGTAGGCATG[C/G]ATAGGTTGCAAAAAG	29116
rs145160701	snp	C/T	5.03808e-05	0.00501875	synonymous-codon	MYLIP	GRCh38.p7	6:16144915	TGACACAGTGACCAG[C/T]GCCGTGATGATGCAG	29116
rs145292846	snp	G/T	9.90279e-05	0.00703592	missense, downstream-variant-500B, utr-variant-5-prime	MYLIP, MIR4639	GRCh38.p7	6:16141707	GCAGTGGAACTCAGT[G/T]CCCTCCTGGCCCAGA	29116
rs145390818	snp	A/C	0.00119737	0.0244387	intron-variant	MYLIP	GRCh38.p7	6:16135808	CTATATAGTGTATAT[A/C]TACAGTATATATTCT	29116
rs145437840	snp	C/G	1.64738e-05	0.00286995	synonymous-codon, intron-variant	MYLIP	GRCh38.p7	6:16130652	AAACCTGAGAAACCG[C/G]ATCTCCCAGCAGATG	29116
rs145540269	snp	C/T	5.13053e-05	0.00506458	synonymous-codon	MYLIP	GRCh38.p7	6:16145278	CTTCTGTCCCTGTGG[C/T]CACACTGTGTGCTGT	29116
rs146183634	snp	C/G	0.00119737	0.0244387	intron-variant	MYLIP	GRCh38.p7	6:16130942	AGTGCATTTTCCAAT[C/G]CTTCTTTTAGTTTTT	29116
rs146292820	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16147972	AGCTAAGGTAAAGCT[A/G]GAAACCTACACTGTC	29116
rs146590862	snp	A/C/G	0.0013384	0.0258351	missense, intron-variant	MYLIP	GRCh38.p7	6:16146671	TCCCAGTCATGTCCC[A/C/G]TCTGCAGGTCGCGTG	29116
rs146833408	snp	C/T	0.00557542	0.0525036	intron-variant	MYLIP	GRCh38.p7	6:16135378	GGTGTGGGTTGTGAT[C/T]ACTTTTGAAGTTGGA	29116
rs146875553	snp	C/G			intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140080	ATGTTCCTCTACCTG[C/G]AATGTCAGACACAGA	29116
rs146887223	snp	C/G	0.000399281	0.0141238	missense	MYLIP	GRCh38.p7	6:16143195	ATCTCAATTTGTAAA[C/G]ATGACTTTAGCCCAA	29116
rs147184996	snp	C/T	0.00993419	0.0697739	intron-variant, downstream-variant-500B	MYLIP, MIR4639	GRCh38.p7	6:16141938	GAGCTCTCTGATGTT[C/T]GAGGCACTTAAGAAG	29116
rs147404910	snp	C/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16136955	TGTCAGATACATGTT[C/T]TGTAAATGTATTTCC	29116
rs147492123	snp	A/G	0.00358779	0.0422022	intron-variant	MYLIP	GRCh38.p7	6:16137472	AATAGCTGCTTAGCT[A/G]TTTTAAAGATGTAGG	29116
rs147637310	snp	C/G	8.26945e-05	0.00642965	synonymous-codon	MYLIP	GRCh38.p7	6:16145206	GCAGGAGAAGCTACG[C/G]AAGCTGAAGGAAGCC	29116
rs147654236	snp	A/T	5.37726e-05	0.00518492	missense, utr-variant-5-prime	MYLIP	GRCh38.p7	6:16143034	GCATTGTTGCAAAAC[A/T]TAAGGAGTTGGAGGG	29116
rs147865230	snp	A/G			upstream-variant-2KB	MYLIP	GRCh38.p7	6:16127398	CCAAGCTTCAGACAG[A/G]TGAAGTAAGTTTTCT	29116
rs147902122	snp	A/G	0.00597247	0.0543191	intron-variant	MYLIP	GRCh38.p7	6:16133684	TTTCCAAAACCAGAG[A/G]TTAGAGAAGTATATG	29116
rs148277683	snp	C/T	0.0126979	0.078662	intron-variant	MYLIP	GRCh38.p7	6:16136856	GTATCTTTTTCAAAG[C/T]GTCCAAGTCATTTAC	29116
rs148485764	in-del	-/G	0.0185938	0.0946107	utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16147744	TCCTTTTCTGTTTTT[-/G]GGGGGGGGAGTTTTG	29116
rs148538197	snp	A/G	0.00835141	0.0640778	intron-variant, downstream-variant-500B	MYLIP, MIR4639	GRCh38.p7	6:16141939	AGCTCTCTGATGTTC[A/G]AGGCACTTAAGAAGT	29116
rs148561418	snp	C/T	0.000610818	0.0174653	synonymous-codon	MYLIP	GRCh38.p7	6:16145158	GAACTGCAGCAGCTG[C/T]GAGGGCCTCAGCTGC	29116
rs148798272	snp	A/T	0.0197687	0.0974348	intron-variant	MYLIP	GRCh38.p7	6:16139148	CCACTTTTGCCTGTA[A/T]TCCCAGCACTTTGGG	29116
rs148878853	snp	C/T	0.000618478	0.0175743	synonymous-codon	MYLIP	GRCh38.p7	6:16145302	GTGCTGTGAGAGCTG[C/T]GCCGCCCAGCTACAG	29116
rs149059329	snp	G/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16144052	GTTTTACCCACAGAA[G/T]GTGCATGTGTGTGAG	29116
rs149200483	snp	A/G	0.00279162	0.0372561	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128083	CTGTAAGGCGTTTTG[A/G]TTCAGCAGAACGAGT	29116
rs149243474	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16141081	AAGGGCTTGGGAAAG[A/G]ATATATGGAGTTTGG	29116
rs149465552	snp	A/G			intron-variant	MYLIP	GRCh38.p7	6:16136111	ACATAAATCCTAATT[A/G]TACCATTTAATGATT	29116
rs149696224	snp	A/G	0.00176107	0.0296215	missense, intron-variant	MYLIP	GRCh38.p7	6:16130620	TTTACGGGTAGCAAA[A/G]GTGAAAGTTTATGGC	29116
rs149725774	snp	C/T			intron-variant	MYLIP	GRCh38.p7	6:16132825	GTTGTAAAATACTTA[C/T]ATAAAATGCCATGAA	29116
rs149751439	snp	A/C	1.68029e-05	0.00289848	missense	MYLIP	GRCh38.p7	6:16145257	CGAGGAGGAGATCAA[A/C]TCCACCTTCTGTCCC	29116
rs149989070	snp	C/T	0.0174175	0.0916809	intron-variant	MYLIP	GRCh38.p7	6:16138227	ATATGTCATCTACTT[C/T]TGATCTTTAGTGCAA	29116
rs150091029	snp	A/G	0.0271762	0.113356	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140633	GACAGAGGGAGCAGC[A/G]AGACCAGAGACACCA	29116
rs150249166	snp	A/G	0.000798403	0.0199641	intron-variant	MYLIP	GRCh38.p7	6:16135022	TGTTGAGCAGCTGTA[A/G]GGACACTAGGTGTGT	29116
rs150429938	snp	C/T	9.88908e-05	0.00703105	missense, intron-variant	MYLIP	GRCh38.p7	6:16143722	ATCCTGTGGTGCAGA[C/T]GGCCACCCAGTCAGG	29116
rs150435024	in-del	-/ATATATCT			intron-variant	MYLIP	GRCh38.p7	6:16135749	TATGTGTGTGTATAC[-/ATATATCT]ATATATATATATATA	29116
rs150598537	snp	A/G	0.000798403	0.0199641	intron-variant	MYLIP	GRCh38.p7	6:16131767	TTGTTTTACCAAAGG[A/G]CTGATAAAGACTCAT	29116
rs150640386	snp	C/T			intron-variant	MYLIP	GRCh38.p7	6:16142405	CCAGCAAGAATTAAA[C/T]CAGGAGATCTAACAT	29116
rs150756832	snp	A/G	0.000181814	0.00953277	missense	MYLIP	GRCh38.p7	6:16145184	GCTGCCAGCAGACCC[A/G]GGTGCTGCAGGAGAA	29116
rs151071456	snp	C/T	0.00716266	0.059414	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16127119	TGTGTGGGAGGATCC[C/T]TCCTTTTTTTTTAGC	29116
rs151123667	snp	A/G/T	0.00716266	0.059414	intron-variant	MYLIP	GRCh38.p7	6:16134145	CTTACGTGGTAATTT[A/G/T]TTTATTATCAGTCAC	29116
rs151166390	snp	C/T	0.00358779	0.0422022	intron-variant	MYLIP	GRCh38.p7	6:16144226	AGGGAACTGGGAGGA[C/T]AATTATTTACTTAGT	29116
rs151199797	snp	C/G	0.000658924	0.0181391	missense	MYLIP	GRCh38.p7	6:16143206	TAAAGATGACTTTAG[C/G]CCAATTAATAGGTAA	29116
rs180797659	snp	A/G			intron-variant	MYLIP	GRCh38.p7	6:16137134	TTTTGTTTCTAAAGC[A/G]TTACGGTTTTAGCTT	29116
rs180810500	snp	C/T	0.0115144	0.0749975	intron-variant	MYLIP	GRCh38.p7	6:16130407	TTGGTATCATTGGAG[C/T]CGTGGAACTTTGTTT	29116
rs181097228	snp	G/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16130001	TTTCCTTAACAGTGA[G/T]GGAGATCGGTGCCAA	29116
rs181113039	snp	C/G	0.00119737	0.0244387	utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16147380	AAAAAGCAGCTCACT[C/G]AATGTGGGTGGCTCC	29116
rs181354077	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16133806	TCTTTGCTAGGAGAC[A/G]TTTTGCTTAGGTAAG	29116
rs181455552	snp	A/C	0.000798403	0.0199641	intron-variant	MYLIP	GRCh38.p7	6:16143526	TCCACATATGCCCAA[A/C]TGCTTTTCACTGTAT	29116
rs181488807	snp	C/T	0.0162398	0.0886349	intron-variant	MYLIP	GRCh38.p7	6:16143344	GATTTCATTTTGGTA[C/T]GTACATTAATTTTAT	29116
rs181726201	snp	A/T	0.000798403	0.0199641	intron-variant	MYLIP	GRCh38.p7	6:16142844	TAGTTGAGATCCCAG[A/T]GTCTTAGACGTTTTT	29116
rs181912298	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16138210	AGCCTCTATTGAATT[A/G]AATATGTCATCTACT	29116
rs182105734	snp	C/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16132047	GTCATAACTTGCAGT[C/T]GAATACAAGATATAA	29116
rs182207557	snp	G/T	0.0130921	0.0798413	intron-variant	MYLIP	GRCh38.p7	6:16129531	CTGCGGCGGCAGCCG[G/T]GGGGAGCGCGTCCCC	29116
rs182215814	snp	C/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16134069	TTGGGAGACTAAACT[C/G]CCCCAAGACATCATG	29116
rs182349314	snp	A/G			intron-variant	MYLIP	GRCh38.p7	6:16131049	AAAAAAAAAAAAAAA[A/G]AAACCACCCTACCCG	29116
rs182479937	snp	C/G	0.000798403	0.0199641	intron-variant	MYLIP	GRCh38.p7	6:16146500	GTATAAACTTTCAAC[C/G]TGTGAGACGGCAAAG	29116
rs182491500	snp	C/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16139457	TCGTTTGTGGCAATA[C/T]TCTTCAAGTCTTTCA	29116
rs182493550	snp	G/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16144105	TACCTCCTACCGTAT[G/T]CTCTTATGCCATTAA	29116
rs182552866	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16135322	TAAGCACATTTTTTT[A/G]GAAGTGCAGATTTTC	29116
rs182730226	snp	A/T	0.0659589	0.169201	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16129065	CCGCTATATCAGCAG[A/T]GTCCCTGTCGCAGCG	29116
rs182801826	snp	A/G	0.000798403	0.0199641	intron-variant	MYLIP	GRCh38.p7	6:16134763	TGGTTATTTCCAAAG[A/G]AAGTATTTAATCAAA	29116
rs183014652	snp	A/C			intron-variant	MYLIP	GRCh38.p7	6:16135729	ATGTATATATACACA[A/C]ATTATATGTGTGTGT	29116
rs183015229	snp	A/G	0.00119737	0.0244387	intron-variant	MYLIP	GRCh38.p7	6:16131409	TAAAACACCACCAAC[A/G]GTGGTAGACAACTGA	29116
rs183049991	snp	C/G	0.00159617	0.0282053	intron-variant	MYLIP	GRCh38.p7	6:16138677	TGTTTACCCTAAAAC[C/G]CCAGCTTAGGGCTGG	29116
rs183311610	snp	C/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16144627	CCATAAGCAACTTCA[C/G]TCAGTAGCGTCTGTC	29116
rs183409081	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140065	ATTCTTACCTTGCTC[A/G]TGTTCCTCTACCTGG	29116
rs183739253	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128703	TCACAACCGAAATGC[A/G]TGCTCAGAGTGATCC	29116
rs183742189	snp	A/G	0.0023933	0.0345097	intron-variant	MYLIP	GRCh38.p7	6:16145626	ATCCAGGCCTCCTGA[A/G]GCCTGGCCCAGGGCT	29116
rs183951201	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16131113	CCGATAGTAACCTCT[A/G]CCTCAGCAGTGTTAC	29116
rs184029155	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16127529	GCACACTGCAGCCTC[A/G]AACTCCCAGGCTCAA	29116
rs184082198	snp	A/G	0.000399281	0.0141238	downstream-variant-500B, intron-variant	MYLIP	GRCh38.p7	6:16148690	TGGTGCTGCTGGTGT[A/G]TGGCCTGCTCAAGAC	29116
rs184160695	snp	C/G	0.00318978	0.0398085	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16141267	TATAGAGTTCCTTAA[C/G]ATTCTATCAGAATCC	29116
rs184429913	snp	C/T	0.00279162	0.0372561	intron-variant	MYLIP	GRCh38.p7	6:16136258	CCCCCACCCACCGCA[C/T]ACCACACCTCTGTCA	29116
rs184672658	snp	C/T	0.00119737	0.0244387	intron-variant	MYLIP	GRCh38.p7	6:16133757	AATCTATATTTTGCT[C/T]CCGACTTAGCCACGT	29116
rs184891518	snp	C/T	0.000461148	0.0151777	synonymous-codon	MYLIP	GRCh38.p7	6:16145083	TGGCGTTGTGGACCT[C/T]GTTTCAAGAAACAAC	29116
rs185042496	snp	A/C/T	0.00119737	0.0244387	utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16146923	CACTGCAAAAACATA[A/C/T]CCATGCGTAGAATCA	29116
rs185139864	snp	C/T	0.0130921	0.0798413	intron-variant	MYLIP	GRCh38.p7	6:16129827	GGCTCGAAGCAGTCT[C/T]GGGCCCCAGGGGTTC	29116
rs185184376	snp	C/T	0.00438332	0.0466095	intron-variant	MYLIP	GRCh38.p7	6:16133954	TTTCAGTGATGCTGG[C/T]AGTGATGAGTTTGAC	29116
rs185389503	snp	A/G	0.000399281	0.0141238	downstream-variant-500B, intron-variant	MYLIP	GRCh38.p7	6:16148539	TATTTATGTCTTTGG[A/G]TGGTTAGATTGGTAT	29116
rs185412324	snp	A/G			intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140970	GAGGTACAAATGGGA[A/G]GATAGAACTGGATTT	29116
rs185427083	snp	A/G	0.00199481	0.0315187	intron-variant	MYLIP	GRCh38.p7	6:16130433	TGTTTTTCCAGTTTA[A/G]ATCAGGAATTGTAAC	29116
rs185566235	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16133417	AGATTTGATTCTTCT[A/G]TCTAGATTATGCTTT	29116
rs185693291	snp	A/G	0.00279162	0.0372561	intron-variant	MYLIP	GRCh38.p7	6:16130134	TTAGCTGACACTTGT[A/G]GCGTGTTCCCTCAAT	29116
rs185701087	snp	C/G	0.0193772	0.0965046	utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16147746	CCTTTTCTGTTTTTG[C/G]GGGGGGAGTTTTGTT	29116
rs185703203	snp	C/G	0.00676609	0.0577691	intron-variant	MYLIP	GRCh38.p7	6:16138232	TCATCTACTTTTGAT[C/G]TTTAGTGCAAAAGCA	29116
rs185799393	snp	C/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16143970	TCAATGAGTCTAGTA[C/T]AGAATTTAAGAAATT	29116
rs185942617	snp	C/T	0.000798403	0.0199641	intron-variant	MYLIP	GRCh38.p7	6:16134868	GCCAAGGAACGCCTG[C/T]CTGGGTATCTTTAGG	29116
rs186185246	snp	A/G	0.000798403	0.0199641	intron-variant	MYLIP	GRCh38.p7	6:16137203	GTTTTACTGAAATTA[A/G]AGATACAAAACAGAA	29116
rs186315221	snp	G/T	0.000798403	0.0199641	intron-variant	MYLIP	GRCh38.p7	6:16139125	ACACCTGAAAAATAA[G/T]TTAAAAGCCACTTTT	29116
rs186938540	snp	C/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16131796	ATTTTGAAATACTTA[C/T]CATTTGAATTTGAAA	29116
rs187088250	snp	A/G	0.00159617	0.0282053	intron-variant	MYLIP	GRCh38.p7	6:16143418	TGTGGCAGAGTTAAC[A/G]TTTTCCAAATAACCC	29116
rs187145853	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16134437	TTTGAACTTAACTTA[A/G]AGCTTCCTCACATTC	29116
rs187175974	snp	G/T	0.00159617	0.0282053	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128502	CGCCTGGCTATTTTG[G/T]TTTTTTTTTTGTATT	29116
rs187644675	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16132184	CTTCAGAAGCTTGGA[A/G]TACCAAATAACTGCA	29116
rs187690525	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16135386	TTGTGATCACTTTTG[A/G]AGTTGGAAATTTTCC	29116
rs187868580	snp	C/G	0.00119737	0.0244387	intron-variant	MYLIP	GRCh38.p7	6:16144127	TGCCATTAATCTAGA[C/G]ACAAAGTGTGTTAGG	29116
rs187882832	snp	A/T			intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16141010	TCAGAGAGAAGAAAG[A/T]CAAGTGAAATAGGAC	29116
rs187957335	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16139579	ATTCACCAAGATGAA[A/G]TTTATCAAATGGTCA	29116
rs188188714	snp	C/G			intron-variant, downstream-variant-500B	MYLIP, MIR4639	GRCh38.p7	6:16142071	GGCCATCAGGACAGA[C/G]GGAGCAGCAAGACCA	29116
rs188470905	snp	A/C	0.000798403	0.0199641	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16127402	GCTTCAGACAGATGA[A/C]GTAAGTTTTCTCTTT	29116
rs188511465	snp	A/C	0.0115144	0.0749975	intron-variant	MYLIP	GRCh38.p7	6:16131173	AAGCAGGAAACAGTT[A/C]CTCTTGGGTTACTTA	29116
rs188594954	snp	A/G			intron-variant	MYLIP	GRCh38.p7	6:16133782	CCACGTTTTAGCAGA[A/G]CTCTGAAGTCTTTGC	29116
rs188712375	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16144707	AAGCCATAATGTCAG[A/G]AGATGTTAGAGAAAC	29116
rs188714131	snp	C/T	0.00478085	0.0486577	intron-variant	MYLIP	GRCh38.p7	6:16135811	TATAGTGTATATATA[C/T]AGTATATATTCTATA	29116
rs189142285	snp	C/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16136396	TGAGATCCATCCATA[C/T]TGTCCTATATATCAG	29116
rs189221319	snp	C/G	0.00199481	0.0315187	intron-variant	MYLIP	GRCh38.p7	6:16134048	GAAAAGTTTCCCTAG[C/G]CTTGCTTGGGAGACT	29116
rs189240678	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16145991	ACTGTGGTTTTATGT[A/G]AAACTGGTTCTAGAT	29116
rs189481765	snp	C/T	0.000399281	0.0141238	synonymous-codon	MYLIP	GRCh38.p7	6:16143140	TTCTGTGCGGGATAG[C/T]GAAGGGCAGAAACTG	29116
rs189866709	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16144027	GTGGAGTCCTTATTA[A/G]TGTAGTCTTGTTTTA	29116
rs189966687	snp	C/G			intron-variant	MYLIP	GRCh38.p7	6:16135260	TTTCAGATTTCAGGG[C/G]TGCCTAGATTGGTGT	29116
rs190023818	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16129859	TGGCAGACAAGCCGG[A/G]CCCTTGTCTCACGCT	29116
rs190041677	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16136799	TGCATTTCTCTGACA[A/G]TTCATATTAAACACT	29116
rs190267377	snp	A/G	0.0023933	0.0345097	intron-variant	MYLIP	GRCh38.p7	6:16137358	CGTGGGTTCTGACAA[A/G]GTGAGAGCAGAACCA	29116
rs190406551	snp	C/T			intron-variant	MYLIP	GRCh38.p7	6:16130199	GCCCAGATAATAAGT[C/T]GCCAAAAATCAGCTG	29116
rs190419186	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16147984	GCTAGAAACCTACAC[C/T]GTCACTTTACTGAGA	29116
rs190508013	snp	A/G	0.00279162	0.0372561	intron-variant	MYLIP	GRCh38.p7	6:16138314	GGTAACATTTTGCCT[A/G]CTTTACAAAAAAAAA	29116
rs190825868	snp	A/T	0.00159617	0.0282053	intron-variant	MYLIP	GRCh38.p7	6:16133423	GATTCTTCTATCTAG[A/T]TTATGCTTTGCTCTT	29116
rs190887823	snp	A/C			downstream-variant-500B, intron-variant	MYLIP	GRCh38.p7	6:16148670	TTAACAATTAACAAC[A/C]CAGCTGGTGCTGCTG	29116
rs190904167	snp	G/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140026	CTCCTTAGATTTGTA[G/T]CCTCACTGCCTCCTC	29116
rs191073335	snp	A/G/T			intron-variant	MYLIP	GRCh38.p7	6:16143481	TAGACATGCATGTGC[A/G/T]CACACCCAGCACTTG	29116
rs191135165	snp	C/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16144371	GCTGCTATCCTGAGT[C/T]GTCACTGTGTATGGA	29116
rs191233106	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128642	ACCATGCCCGGACGA[A/G]AACAGTTTTCTTTAG	29116
rs191241452	snp	A/G	4.95503e-05	0.00497722	missense	MYLIP	GRCh38.p7	6:16145163	GCAGCAGCTGCGAGG[A/G]CCTCAGCTGCCAGCA	29116
rs191560627	snp	A/G	0.0162398	0.0886349	intron-variant	MYLIP	GRCh38.p7	6:16139320	TTGAACCCAGGAGGC[A/G]GAGCTTGCAGTGAGC	29116
rs191601860	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16131240	AGTGTGCAGCCAAGA[A/G]CTCTGTTTGACTTCA	29116
rs191649152	snp	A/G			intron-variant	MYLIP	GRCh38.p7	6:16136474	AGTGTTTGTTTATCC[A/G]TACTCCTAATAATGA	29116
rs191791611	snp	C/T	0.00358779	0.0422022	intron-variant	MYLIP	GRCh38.p7	6:16132023	TTTGTGAAAGCTTTG[C/T]GCTTCACTGTCATAA	29116
rs192153129	snp	A/G	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140697	GAGGAATCGTTCCCT[A/G]TCCTGGGGCATAGCA	29116
rs192181184	snp	C/T	0.00159617	0.0282053	intron-variant	MYLIP	GRCh38.p7	6:16130495	CTTAGCCTCAGGGAG[C/T]CGTTGGGTTTGCTTT	29116
rs192300994	snp	C/G	0.00199481	0.0315187	intron-variant	MYLIP	GRCh38.p7	6:16135571	CAAGCCCTCCATGAA[C/G]TAGATAGATGTGGTG	29116
rs192428273	snp	C/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16134593	GTTATAGCATCACTT[C/T]AACTGCAACCCATTT	29116
rs192551516	snp	A/C	0.00557542	0.0525036	intron-variant	MYLIP	GRCh38.p7	6:16144708	AGCCATAATGTCAGG[A/C]GATGTTAGAGAAACA	29116
rs192609355	snp	A/G			intron-variant	MYLIP	GRCh38.p7	6:16136025	TAAGTATGTTTCCCC[A/G]TAAATACTTCAGCAT	29116
rs192851409	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16127483	GTCTTTTGCTCTGTC[A/G]CCTAGGCTGGAGTGC	29116
rs192884969	snp	A/G	0.00279162	0.0372561	intron-variant	MYLIP	GRCh38.p7	6:16133445	TTTGCTCTTGAATAT[A/G]AGCCTCAAATGTAAA	29116
rs192952732	snp	C/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16141058	TCCGTGGTCTCCATT[C/T]GGAGAAAAAGGGCTT	29116
rs193212018	snp	C/T	0.00119737	0.0244387	intron-variant	MYLIP	GRCh38.p7	6:16132600	TGGGGTTGGCTGAAA[C/T]ACATAACTGACACTT	29116
rs199606233	snp	C/T			upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128298	TTCTCTTTTTTTTTT[C/T]TTTTTTCTTTTTCTT	29116
rs199758517	snp	A/G	0.000210314	0.0102524	missense, intron-variant	MYLIP	GRCh38.p7	6:16146684	CCGTCTGCAGGTCGC[A/G]TGTGGAGCATGTCCA	29116
rs199776727	snp	C/T	0.000939516	0.0216535	missense	MYLIP	GRCh38.p7	6:16145118	GCCCTTCACACTCGC[C/T]TCTGAAGTCCTCAGA	29116
rs199830608	in-del	-/C/CATGGCAGAG			intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140851	AGAAATGACAAGTTT[-/C/CATGGCAGAG]ATACTAGAAACAAGC	29116
rs199839843	snp	A/G	0.000399281	0.0141238	missense, intron-variant	MYLIP	GRCh38.p7	6:16130728	GTGGAGCCTCATCTC[A/G]TCTTACAGGAGCAGA	29116
rs199922789	snp	C/T			utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16146886	AAAAAAAAAAAGGAA[C/T]AAAAATAACACAGCT	29116
rs199943196	snp	A/G	1.64762e-05	0.00287016	missense, intron-variant	MYLIP	GRCh38.p7	6:16143808	TTTAAAATGATCAGC[A/G]CCAGGGCGGCCAGCG	29116
rs199952798	in-del	-/TC			intron-variant	MYLIP	GRCh38.p7	6:16135759	ATACATATATCTATA[-/TC]TATATATATATATAT	29116
rs200099792	snp	A/C/T	7.00053e-05	0.00591597	intron-variant	MYLIP	GRCh38.p7	6:16144877	TGGTGTTAAAGTAGA[A/C/T]GTTCAATCTTGCCTT	29116
rs200398550	snp	C/T	0.000399281	0.0141238	missense	MYLIP	GRCh38.p7	6:16145142	CCTCAGAAAGCAGCA[C/T]GAACTGCAGCAGCTG	29116
rs200552688	snp	C/T			upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128305	TTTTTTTTCTTTTTT[C/T]TTTTTCTTTTCTTTT	29116
rs200911398	in-del	-/TATA			intron-variant	MYLIP	GRCh38.p7	6:16135756	GTGTATACATATATC[-/TATA]TATATATATATATAT	29116
rs201021082	snp	C/T	0.000104943	0.00724295	missense, utr-variant-5-prime	MYLIP	GRCh38.p7	6:16129372	TGATGGAGGTGGAGG[C/T]GGAGGCGAAAGCCAA	29116
rs201036784	snp	A/G	8.28082e-05	0.00643407	intron-variant	MYLIP	GRCh38.p7	6:16143875	ACAGGCACGTATCTC[A/G]TGTGCTTGGTCACCT	29116
rs201074525	in-del	-/T			downstream-variant-500B, intron-variant	MYLIP	GRCh38.p7	6:16148511	GGAGATCACTTCACC[-/T]AGGTTATTCTCTTAT	29116
rs201087709	snp	A/G	0.000181185	0.00951628	missense	MYLIP	GRCh38.p7	6:16145072	CTGTACAATGCTGGC[A/G]TTGTGGACCTCGTTT	29116
rs201093222	snp	A/G	0.000127847	0.0079942	synonymous-codon, intron-variant	MYLIP	GRCh38.p7	6:16146682	TCCCGTCTGCAGGTC[A/G]CGTGTGGAGCATGTC	29116
rs201162030	snp	A/T	0.000115313	0.0075923	missense	MYLIP	GRCh38.p7	6:16143106	TGTCGGCAATGGAAA[A/T]CTATGGCATAGAATG	29116
rs201528429	snp	C/T			upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128311	TTCTTTTTTCTTTTT[C/T]TTTTCTTTTTTTTTT	29116
rs201753631	in-del	-/TA	0.247905	0.249991	intron-variant	MYLIP	GRCh38.p7	6:16135756	GTGTATACATATATC[-/TA]TATATATATATATAT	29116
rs201781624	snp	C/T	4.94328e-05	0.00497131	missense, intron-variant	MYLIP	GRCh38.p7	6:16143815	TGATCAGCACCAGGG[C/T]GGCCAGCGGGCTCTA	29116
rs201953912	snp	C/T	0.000181188	0.00951636	missense	MYLIP	GRCh38.p7	6:16143132	GAATGGCATTCTGTG[C/T]GGGATAGCGAAGGGC	29116
rs202197437	snp	A/G	0.00199792	0.0315431	missense, intron-variant	MYLIP	GRCh38.p7	6:16143779	AGGAATCTGGGAACA[A/G]CATCGTGCTCTTGTT	29116
rs367710344	snp	A/G	4.95111e-05	0.00497525	intron-variant	MYLIP	GRCh38.p7	6:16143247	AACTTTTTTTGACCT[A/G]AGCATGTGTATACAT	29116
rs367883895	snp	C/T			intron-variant	MYLIP	GRCh38.p7	6:16138749	GAAAAGGTTGCTTTA[C/T]AGCCATGAAACTGCA	29116
rs367915201	snp	C/T			intron-variant	MYLIP	GRCh38.p7	6:16144754	AGAATATTTACCAGA[C/T]GTAAAACTGGAAGGA	29116
rs368166054	snp	G/T	0.000153988	0.00877328	intron-variant	MYLIP	GRCh38.p7	6:16145324	CAGCTACAGGTAGGG[G/T]AGTCAGCTGCCCACT	29116
rs368193746	snp	G/T			intron-variant	MYLIP	GRCh38.p7	6:16144243	ATTATTTACTTAGTC[G/T]AGGACTCAGCTTCAA	29116
rs368335606	snp	C/G			intron-variant	MYLIP	GRCh38.p7	6:16129821	TGGAGTGGCTCGAAG[C/G]AGTCTCGGGCCCCAG	29116
rs368514713	snp	C/T			intron-variant	MYLIP	GRCh38.p7	6:16143571	AGCATTATGGTGATG[C/T]GATAACCCCAGAGGA	29116
rs368658363	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16148120	GGCACATATTAGCAT[A/G]TAAGCCTTTATTCCA	29116
rs368767683	snp	A/G	0.000153988	0.00877328	missense, utr-variant-5-prime	MYLIP	GRCh38.p7	6:16143021	TTGGTGTCCTCCAGC[A/G]TTGTTGCAAAACATA	29116
rs368854977	snp	G/T			upstream-variant-2KB	MYLIP	GRCh38.p7	6:16127638	TGTGTAGAGATGGGG[G/T]TTCGCTGTGTTGCGA	29116
rs368981890	snp	C/T	0.000153988	0.00877328	intron-variant	MYLIP	GRCh38.p7	6:16143660	TGGTGAAGAATCACT[C/T]CTTCTAGATCTGCTT	29116
rs369085168	snp	G/T			intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140736	GAATGACAGGAGACG[G/T]GGCTGGAAAGCTGGG	29116
rs369174288	snp	A/G	0.000230787	0.0107397	synonymous-codon, intron-variant	MYLIP	GRCh38.p7	6:16143837	CGGGCTCTACCGAGC[A/G]ATAACAGAGACGCAC	29116
rs369548845	snp	C/T	0.000208765	0.0102146	intron-variant, nc-transcript-variant	MYLIP, MIR4639	GRCh38.p7	6:16141601	TATCCCCAAGCATAA[C/T]CTCACTCTCACCTTG	29116
rs369689595	snp	C/T			intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16141123	CCAAAATTGAGGTAC[C/T]GAAGAACATCCAGGT	29116
rs369953221	in-del	-/T			intron-variant	MYLIP	GRCh38.p7	6:16134514	TTTATTGTGGCTATT[-/T]AGTTCTTTCCTAAAA	29116
rs370060410	snp	C/G			upstream-variant-2KB	MYLIP	GRCh38.p7	6:16127687	CTGCTGGGCTCAGGC[C/G]ATCCTCCTGCCTCGG	29116
rs370210922	snp	C/T	0.00199481	0.0315187	intron-variant	MYLIP	GRCh38.p7	6:16139405	AAAAAAAAAAAAAGG[C/T]CACTTTTACATAAGC	29116
rs370211572	snp	C/T	0.000798403	0.0199641	intron-variant	MYLIP	GRCh38.p7	6:16136254	CCCACCCCCACCCAC[C/T]GCACACCACACCTCT	29116
rs370365355	snp	A/C/T	0.000330281	0.0128466	synonymous-codon	MYLIP	GRCh38.p7	6:16145164	CAGCAGCTGCGAGGG[A/C/T]CTCAGCTGCCAGCAG	29116
rs370693513	snp	A/G	0.000115332	0.00759293	synonymous-codon, utr-variant-5-prime	MYLIP	GRCh38.p7	6:16143095	TTTGCAGATTGTGTC[A/G]GCAATGGAAAACTAT	29116
rs370798995	snp	A/G			intron-variant	MYLIP	GRCh38.p7	6:16135642	TAAGGGATTTTTACT[A/G]GTATTACTTCCTTAA	29116
rs370834955	snp	C/T	0.00024524	0.0110707	intron-variant	MYLIP	GRCh38.p7	6:16146618	ACACAGGCCCCCCAC[C/T]GAGGCTTGCATGCTA	29116
rs370970158	snp	A/C	0.000153988	0.00877328	intron-variant	MYLIP	GRCh38.p7	6:16142996	TCTGTATACTTAATT[A/C]TCTGTCCTCTTGGTG	29116
rs370972596	snp	C/T			intron-variant	MYLIP	GRCh38.p7	6:16137339	CAGGCTGGCTGATGA[C/T]CACCGTGGGTTCTGA	29116
rs371043452	snp	G/T			utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16147744	GTCCTTTTCTGTTTT[G/T]GGGGGGGGAGTTTTG	29116
rs371111123	snp	A/G			intron-variant	MYLIP	GRCh38.p7	6:16129900	CTGCTGCTCTCAAAT[A/G]CACCGTTCACCTGCA	29116
rs371230170	snp	A/G	0.000153988	0.00877328	missense, intron-variant	MYLIP	GRCh38.p7	6:16143823	ACCAGGGCGGCCAGC[A/G]GGCTCTACCGAGCGA	29116
rs371333019	snp	A/G	4.94238e-05	0.00497086	missense, intron-variant	MYLIP	GRCh38.p7	6:16130671	TCCCAGCAGATGGAT[A/G]GGCTAGCCCCTTACA	29116
rs371339543	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16144467	GGACTCACGTATTTG[A/G]ACAATTAAAGCTAAG	29116
rs371556203	snp	A/C	0.000153988	0.00877328	intron-variant	MYLIP	GRCh38.p7	6:16146640	TGCATGCTAACAGAG[A/C]CTGTTGGCTTTTCTT	29116
rs371593218	snp	C/T	0.000215251	0.010372	intron-variant	MYLIP	GRCh38.p7	6:16143688	CTTTCTTTTCTCTTC[C/T]TGTCTCTTAGGATAG	29116
rs371830283	snp	C/T	2.83942e-05	0.00376779	intron-variant	MYLIP	GRCh38.p7	6:16143002	TACTTAATTCTCTGT[C/T]CTCTTGGTGTCCTCC	29116
rs372057734	snp	C/T	3.3849e-05	0.0041138	intron-variant	MYLIP	GRCh38.p7	6:16130515	GGGTTTGCTTTGATA[C/T]GTACCATTTGCTCAT	29116
rs372152789	snp	C/T	1.64814e-05	0.00287061	synonymous-codon	MYLIP	GRCh38.p7	6:16143215	CTTTAGCCCAATTAA[C/T]AGGTAAGCCAAGACT	29116
rs372194247	snp	C/T			downstream-variant-500B, intron-variant	MYLIP	GRCh38.p7	6:16148684	CCCAGCTGGTGCTGC[C/T]GGTGTGTGGCCTGCT	29116
rs372291333	snp	A/C			intron-variant	MYLIP	GRCh38.p7	6:16139525	ATTTTAGTTTCCTAA[A/C]AGCACACCTCCACCC	29116
rs372428536	snp	C/T			intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140569	AGGATTTGCATGTGA[C/T]ACAGACCAAAGGGTA	29116
rs372465758	snp	C/T			intron-variant	MYLIP	GRCh38.p7	6:16139016	TGGCCACTGTCTCTC[C/T]GGAAGTGTAGGCATG	29116
rs372500760	snp	A/C			upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128741	TTGAAGAACAGTGGC[A/C]GCTTGGAGGTGTTTA	29116
rs372617777	snp	C/T	3.29451e-05	0.00405851	synonymous-codon	MYLIP	GRCh38.p7	6:16145065	GAGGGCTCTGTACAA[C/T]GCTGGCGTTGTGGAC	29116
rs372621278	snp	A/C	0.00119737	0.0244387	intron-variant	MYLIP	GRCh38.p7	6:16138959	CTCTCAGGCTGCCTG[A/C]CACCTGTTTACATTC	29116
rs372719392	in-del	-/TC			intron-variant	MYLIP	GRCh38.p7	6:16135754	GTGTGTATACATATA[-/TC]TATATATATATATAT	29116
rs372779504	snp	A/G			intron-variant	MYLIP	GRCh38.p7	6:16134863	TTTCAGCCAAGGAAC[A/G]CCTGTCTGGGTATCT	29116
rs373110579	snp	A/T			intron-variant	MYLIP	GRCh38.p7	6:16134104	TTTCCTTTATAGCAT[A/T]TAATGAGCTTATAAT	29116
rs373487019	in-del	-/CA			intron-variant	MYLIP	GRCh38.p7	6:16146291	TGAGCTAAGGACACA[-/CA]ATTTCAAGAAGGGTC	29116
rs373541110	snp	A/G			intron-variant	MYLIP	GRCh38.p7	6:16146022	AATACTTAGTCCTTC[A/G]GAAGCTGCTAATTTC	29116
rs373554271	snp	A/G	0.00279162	0.0372561	intron-variant	MYLIP	GRCh38.p7	6:16130490	GCAATCTTAGCCTCA[A/G]GGAGCCGTTGGGTTT	29116
rs373640110	snp	C/T	0.00914312	0.0669923	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16127592	GAGACTACAGGCAGG[C/T]GCCACCACGCCTGGC	29116
rs373942444	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16147298	GGAAGGCAAACAGGT[C/T]TACAAATCAATTCTG	29116
rs373945462	snp	C/G	3.62707e-05	0.0042584	intron-variant, nc-transcript-variant	MYLIP, MIR4639	GRCh38.p7	6:16141583	CTGAGATTGATGTCA[C/G]GTTATCCCCAAGCAT	29116
rs374072017	snp	C/T	1.64741e-05	0.00286998	synonymous-codon, intron-variant	MYLIP	GRCh38.p7	6:16143783	ATCTGGGAACAGCAT[C/T]GTGCTCTTGTTTAAA	29116
rs374211332	snp	A/G			intron-variant	MYLIP	GRCh38.p7	6:16136466	ATGAATCTAGTGTTT[A/G]TTTATCCGTACTCCT	29116
rs374247471	snp	C/T	1.70472e-05	0.00291947	intron-variant, nc-transcript-variant	MYLIP, MIR4639	GRCh38.p7	6:16141612	ATAACCTCACTCTCA[C/T]CTTGCTTTGCAGGCA	29116
rs374261222	snp	A/G	7.21957e-05	0.00600771	intron-variant	MYLIP	GRCh38.p7	6:16145320	CGCCCAGCTACAGGT[A/G]GGGGAGTCAGCTGCC	29116
rs374453156	snp	A/G			upstream-variant-2KB	MYLIP	GRCh38.p7	6:16127701	CGATCCTCCTGCCTC[A/G]GCCTCCAAAAGTGCT	29116
rs374504865	snp	A/G			intron-variant	MYLIP	GRCh38.p7	6:16129902	GCTGCTCTCAAATGC[A/G]CCGTTCACCTGCATC	29116
rs374523605	snp	C/T	0.000128186	0.00800478	intron-variant	MYLIP	GRCh38.p7	6:16143017	CCTCTTGGTGTCCTC[C/T]AGCATTGTTGCAAAA	29116
rs374618899	in-del	-/A	0.00953873	0.0683987	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128355	TTTTTGAGACAGGGT[-/A]TTTTTGCTCTTCTTG	29116
rs374712005	snp	A/G	1.65364e-05	0.0028754	synonymous-codon	MYLIP	GRCh38.p7	6:16145200	GGTGCTGCAGGAGAA[A/G]CTACGCAAGCTGAAG	29116
rs374824528	snp	A/G			intron-variant	MYLIP	GRCh38.p7	6:16146131	CTGACTCTCATCCCT[A/G]AGTCTCTCCTGAGGG	29116
rs374825715	snp	A/T	0.000798403	0.0199641	intron-variant	MYLIP	GRCh38.p7	6:16142498	CAAAAATTGTCTCAC[A/T]GTTCTGTAGGTCAGG	29116
rs375497721	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140481	TACATTTTTGGAGCT[C/T]TCTGATGTTCGAGGC	29116
rs375822613	multinucleotide-polymorphism	AG/TA			downstream-variant-500B, intron-variant	MYLIP	GRCh38.p7	6:16148512	GGAGATCACTTCACC[AG/TA]GTTATTCTCTTATTT	29116
rs375904103	snp	A/T	5.22189e-05	0.00510947	intron-variant	MYLIP	GRCh38.p7	6:16130779	TAAACCAATGTCAAA[A/T]TGACCTTTGGTTCCC	29116
rs375950856	snp	A/G			intron-variant	MYLIP	GRCh38.p7	6:16142867	ACGTTTTTTATAGTA[A/G]GTTCGCTAAATACAT	29116
rs376233390	snp	A/G			intron-variant	MYLIP	GRCh38.p7	6:16139025	TCTCTCCGGAAGTGT[A/G]GGCATGGATAGGTTG	29116
rs376385408	snp	C/T	0.000153988	0.00877328	missense	MYLIP	GRCh38.p7	6:16145067	GGGCTCTGTACAATG[C/T]TGGCGTTGTGGACCT	29116
rs376620126	snp	C/T	0.000153988	0.00877328	intron-variant	MYLIP	GRCh38.p7	6:16143889	CGTGTGCTTGGTCAC[C/T]TCAGCACCACAGCTC	29116
rs376744762	snp	A/C/T	6.87136e-05	0.00586112	intron-variant	MYLIP	GRCh38.p7	6:16130768	GTGAGCTAAAATAAA[A/C/T]CAATGTCAAATTGAC	29116
rs376987781	snp	C/T			intron-variant	MYLIP	GRCh38.p7	6:16139381	CGACAGAGCAAGACT[C/T]CATCTCAAAAAAAAA	29116
rs377154869	snp	A/G			intron-variant	MYLIP	GRCh38.p7	6:16131180	AAACAGTTCCTCTTG[A/G]GTTACTTAAACTTGG	29116
rs377214864	snp	C/T	4.96956e-05	0.00498451	intron-variant	MYLIP	GRCh38.p7	6:16143687	GCTTTCTTTTCTCTT[C/T]CTGTCTCTTAGGATA	29116
rs377351131	snp	A/G	0.000115596	0.00760164	missense	MYLIP	GRCh38.p7	6:16145159	AACTGCAGCAGCTGC[A/G]AGGGCCTCAGCTGCC	29116
rs377395123	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16146975	GGAGGAGCTCTGGGA[C/T]GCAGACACATTCCTT	29116
rs377500226	snp	A/G			intron-variant	MYLIP	GRCh38.p7	6:16136531	AAAGCTGCCATAAAC[A/G]TTCTAGTATGTACCT	29116
rs377522751	snp	A/C/T	6.60419e-05	0.00574606	missense, stop-gained, downstream-variant-500B, utr-variant-5-prime	MYLIP, MIR4639	GRCh38.p7	6:16141719	AGTGCCCTCCTGGCC[A/C/T]AGACCAAGTTTGGAG	29116
rs377575633	snp	C/T	9.17768e-05	0.00677348	synonymous-codon, intron-variant	MYLIP	GRCh38.p7	6:16146670	TTCCCAGTCATGTCC[C/T]GTCTGCAGGTCGCGT	29116
rs377668250	snp	A/G			utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16147545	AGACTGAAAACAGAG[A/G]GCACTCTCCTTGGGA	29116
rs377679593	in-del	-/T			intron-variant	MYLIP	GRCh38.p7	6:16131758	TTTGCTTGTTTGTTT[-/T]ACCAAAGGACTGATA	29116
rs386697472	multinucleotide-polymorphism	ACA/CCG			upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128349	TTTTTTTTTTTTGAG[ACA/CCG]GGGTTTTTTGCTCTT	29116
rs397971095	in-del	-/AA			utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16146881	TAAAAAAAAAAAAAA[-/AA]GGAAGAAAAATAACA	29116
rs527249348	snp	A/T	0.00119737	0.0244387	intron-variant	MYLIP	GRCh38.p7	6:16145711	TATTACTTAAGATAT[A/T]TGGGAAAGAATACTT	29116
rs527284107	snp	C/T	0.0023933	0.0345097	intron-variant	MYLIP	GRCh38.p7	6:16144734	AAACAGAGGTGTAAT[C/T]ACTGAGAATATTTAC	29116
rs527319455	snp	A/G			intron-variant	MYLIP	GRCh38.p7	6:16142416	TAAACCAGGAGATCT[A/G]ACATAGGCATTTTAG	29116
rs527565093	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16139052	GTTGCAAAAAGACAC[A/G]GAATTGATTCAAAAC	29116
rs527629616	snp	A/G	1.65946e-05	0.00288046	missense	MYLIP	GRCh38.p7	6:16145238	TGCTGTGCATGGTGT[A/G]CTGCGAGGAGGAGAT	29116
rs527743997	snp	C/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16139113	GTCTCTAACTTTACA[C/T]CTGAAAAATAAGTTA	29116
rs528118507	in-del	-/ATG	0.0123036	0.0774623	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140860	AAGTTTATACTAGAA[-/ATG]ACAAGCAGCATGGAA	29116
rs528154321	snp	C/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16132179	TAAATCTTCAGAAGC[C/T]TGGAGTACCAAATAA	29116
rs528361666	snp	A/C			intron-variant	MYLIP	GRCh38.p7	6:16145462	TGTATTTGGTGACCT[A/C]AAAGGCATTGCCCTT	29116
rs528479599	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	MYLIP, MIR4639	GRCh38.p7	6:16142113	GCATGAACATGGCAG[C/T]ATCAGGGCTACTGCA	29116
rs528646507	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16127217	AAGGGGGGTAGGGAC[A/G]GGAAAAGTCATCATT	29116
rs528692384	snp	C/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16136097	TTGATGTAAAATTTA[C/T]ATAAATCCTAATTAT	29116
rs528758805	snp	A/G	0.000798403	0.0199641	intron-variant	MYLIP	GRCh38.p7	6:16135284	TTGGTGTTTGCCTAG[A/G]ATGGGGATCTACTGT	29116
rs529228225	snp	C/G			intron-variant	MYLIP	GRCh38.p7	6:16142669	TCCCTGGCCACAGGG[C/G]CCTCAGGGGTCAACT	29116
rs529252958	snp	C/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16132454	ATAATAGTACTCAAA[C/G]AATGTACATACCTAG	29116
rs529263458	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16129081	GTCCCTGTCGCAGCG[C/G]AGGCAGTTGGGCTGC	29116
rs529329092	snp	A/G	0.00159617	0.0282053	utr-variant-5-prime, upstream-variant-2KB	MYLIP	GRCh38.p7	6:16129166	GGGTGGCGGGGACGC[A/G]AGTGGCGGCCGCGGG	29116
rs529642562	snp	C/T	0.000798403	0.0199641	intron-variant	MYLIP	GRCh38.p7	6:16146122	CCACCTATTCTGACT[C/T]TCATCCCTAAGTCTC	29116
rs529726811	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16145390	GGGAGTAGGAGCCAG[A/G]TACTGGCTCGCTAAT	29116
rs529902686	snp	C/T			downstream-variant-500B, intron-variant	MYLIP	GRCh38.p7	6:16148344	CTACTTTCCTCCTAC[C/T]GGGAATTTAATTTTT	29116
rs530660414	snp	C/T			intron-variant	MYLIP	GRCh38.p7	6:16146117	TCTGCCCACCTATTC[C/T]GACTCTCATCCCTAA	29116
rs530835028	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16143565	TAAGGCAGCATTATG[A/G]TGATGTGATAACCCC	29116
rs530895928	snp	C/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16136304	GAGATGAGCTATGCC[C/T]GTGCGGCCTTATCTA	29116
rs530897526	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16142872	TTTTATAGTAAGTTC[A/G]CTAAATACATGAAAC	29116
rs531047139	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128178	GCTGCAAAAACTTTC[A/T]TACTCAGATTTTGTT	29116
rs531108405	snp	C/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16136913	TGAGTTGTACAAATT[C/T]TTCATGTACCCTAGA	29116
rs531245511	snp	G/T			utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16147747	CTTTTCTGTTTTTGG[G/T]GGGGGAGTTTTGTTG	29116
rs531259441	snp	A/G	0.000177554	0.00942047	missense	MYLIP	GRCh38.p7	6:16145306	TGTGAGAGCTGCGCC[A/G]CCCAGCTACAGGTAG	29116
rs531421214	snp	A/G			intron-variant	MYLIP	GRCh38.p7	6:16135355	CTTTCAATTAGAAGT[A/G]TTCTTCTGGTGTGGG	29116
rs531490250	snp	A/G	0.00279162	0.0372561	utr-variant-5-prime	MYLIP	GRCh38.p7	6:16129179	GCGAGTGGCGGCCGC[A/G]GGGCCCCGGACAAGG	29116
rs531494844	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16138864	AGGCTAGAATGTGGA[A/G]TATGTCGAAAAGGTC	29116
rs531556585	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16138150	TAAGACAGAGAAAAC[A/G]GTTTTTTTCCAAAGG	29116
rs531983116	snp	A/G			intron-variant	MYLIP	GRCh38.p7	6:16139500	TTCTTTAACGAAAGC[A/G]TAGATGCAGATTTTA	29116
rs532001203	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140624	GGCCCTCAGGACAGA[A/G]GGAGCAGCAAGACCA	29116
rs532058950	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140095	GAATGTCAGACACAG[A/G]TATATTATTAAACAG	29116
rs532153586	snp	C/T	0.000798403	0.0199641	intron-variant	MYLIP	GRCh38.p7	6:16146359	TGTAGAGACCACATT[C/T]TGCACAGAAAGACGT	29116
rs532240853	snp	C/T			intron-variant	MYLIP	GRCh38.p7	6:16145646	GGCCCAGGGCTGCTT[C/T]CTCTATTTCAAGTTG	29116
rs532257839	snp	A/G			utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16147937	CGGGAGACCTAGATG[A/G]CCTTATCGGGTGCAA	29116
rs532269640	snp	C/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16133199	CCATCCAGACTGCTA[C/T]GGGCCCAGCTCTACA	29116
rs532377553	snp	C/T	0.0023933	0.0345097	intron-variant	MYLIP	GRCh38.p7	6:16132126	TTATTTCAAGATCTC[C/T]AGATGCAACCCAGTT	29116
rs532773127	snp	A/C	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16142736	ACTTTCCAATATGTA[A/C]ATTTGACTTATGTAT	29116
rs532837408	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	MYLIP, MIR4639	GRCh38.p7	6:16141942	TCTCTGATGTTCGAG[A/G]CACTTAAGAAGTCAT	29116
rs533109621	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128255	AGCAACCCACTGTGG[C/T]TAATCCTGGTGGAAA	29116
rs533171929	snp	C/T	0.000798403	0.0199641	intron-variant	MYLIP	GRCh38.p7	6:16137138	GTTTCTAAAGCGTTA[C/T]GGTTTTAGCTTTTAC	29116
rs533193153	snp	C/T			intron-variant	MYLIP	GRCh38.p7	6:16135336	TAGAAGTGCAGATTT[C/T]CTGCTTTCAATTAGA	29116
rs533205293	snp	A/G			intron-variant	MYLIP	GRCh38.p7	6:16132903	CCAGTTATGAAAGGT[A/G]ATTTTTTTATTCTTT	29116
rs533248503	snp	C/G	0.00318978	0.0398085	intron-variant	MYLIP	GRCh38.p7	6:16144056	TACCCACAGAAGGTG[C/G]ATGTGTGTGAGCTGC	29116
rs533443010	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16129024	GAGGCCGTGATTGGC[G/T]GGGACCCGAGCTGAA	29116
rs533667537	snp	C/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16137968	TTAGCCAGAATGTTA[C/T]GCCTTGGGCCCCAAA	29116
rs533840069	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140289	TCTACAGCAGTTTAG[A/G]TGCTCTTCAGAGTTT	29116
rs534124347	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128659	ACAGTTTTCTTTAGG[C/T]TTTGGGTTGCTCCTT	29116
rs534219756	snp	G/T			intron-variant	MYLIP	GRCh38.p7	6:16130149	GGCGTGTTCCCTCAA[G/T]GTGTTTGATTTTTGG	29116
rs534251987	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16145513	ATACTATTTTCAACA[A/G]CATAATTACTCCAAA	29116
rs534407252	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140147	ACCTGGCCAAAGTTA[C/G]AATTCATTTGTTAAT	29116
rs534506054	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16147497	TAGTCAAGTACTCCC[C/T]GGGCCTTCTGAGCTG	29116
rs534817839	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16148126	TATTAGCATATAAGC[C/G]TTTATTCCAAGAGGT	29116
rs534832718	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140906	TGGAGTCTGGAGGAG[A/G]AGAGCAGCGCAGAGA	29116
rs534963815	snp	C/T			utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16147626	TGAGGGTAGTTAACT[C/T]ATCACTTCTCCCAAG	29116
rs535019080	snp	G/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16133628	TTCTTGCCTTTCAAA[G/T]GCTTTGAGTTTACTG	29116
rs535080750	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16141424	TTGTTTGGGTCACAA[A/C]TTTTATTCCAGAGAA	29116
rs535292999	snp	A/G	0.000798403	0.0199641	intron-variant	MYLIP	GRCh38.p7	6:16136615	TGGAATAGCTGGGTC[A/G]TGGAGTAAGTAATCA	29116
rs535461843	in-del	-/GGT			intron-variant	MYLIP	GRCh38.p7	6:16130897	AGGTCCTTTTGTTGA[-/GGT]GGTGGAGGGGGAGCT	29116
rs535469108	in-del	-/AGTTAACTTATT	0.00398564	0.0444627	intron-variant	MYLIP	GRCh38.p7	6:16133045	CAAGTTGGGAAGGGC[-/AGTTAACTTATT]AGTTCATATCAGATT	29116
rs535532140	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128479	GGGATTACAGGTGCC[C/T]GCCACCACGCCTGGC	29116
rs535891936	snp	A/G	0.000798403	0.0199641	intron-variant	MYLIP	GRCh38.p7	6:16129572	GGGCGTGGGGCGCGC[A/G]GTCTCCTCCTGGCGC	29116
rs535950252	snp	A/C	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16138312	TTGGTAACATTTTGC[A/C]TACTTTACAAAAAAA	29116
rs536590946	snp	A/C	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140217	ATGACAAGTCATCGA[A/C]GGAAGGTTAAAACTT	29116
rs536656069	snp	A/C	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16146572	TGATTTAGAAAATTA[A/C]ATGCACTAGAGACCA	29116
rs536856690	snp	A/C	1.65021e-05	0.00287241	missense, downstream-variant-500B, utr-variant-5-prime	MYLIP, MIR4639	GRCh38.p7	6:16141671	CTCTTGGCAGGCCAC[A/C]TCTTGTGTTCCCCAG	29116
rs536935922	snp	C/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140727	AGCTGCAGGGAATGA[C/G]AGGAGACGTGGCTGG	29116
rs536993573	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16147321	CAATTCTGTGACTTT[A/T]AAAAAGTTGACAATG	29116
rs537074799	snp	G/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16135354	GCTTTCAATTAGAAG[G/T]GTTCTTCTGGTGTGG	29116
rs537194234	snp	A/C	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16142144	TATATTCATAGAGCT[A/C]TCAAATGTATAAGCA	29116
rs537535150	snp	C/T	0.000798403	0.0199641	intron-variant	MYLIP	GRCh38.p7	6:16134285	TAAACAAAAATGGGG[C/T]TAACTGATAACTACT	29116
rs537664937	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128571	GGTCTCGAATCTGAC[C/T]TCAGGTGATCCACCC	29116
rs538057748	snp	A/C	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16145425	AGACGGGGAATGCCC[A/C]TCTTCACCCGGAAAG	29116
rs538057814	snp	C/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16138417	TACTTGATTCAAAAC[C/T]ACCCATAAATATTGA	29116
rs538126284	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16127808	GGCTCCTATAAAGAA[A/G]TCAAAAAGGTAGGCT	29116
rs538187130	snp	C/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16136702	ATTCTGTACTCCCAG[C/G]AAGAATGTAAGAGTC	29116
rs538189243	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16144210	CCTAATGTTAAAGAT[A/G]AGGGAACTGGGAGGA	29116
rs538392230	snp	A/G	0.00517822	0.0506191	intron-variant	MYLIP	GRCh38.p7	6:16139313	GAATCGCTTGAACCC[A/G]GGAGGCGGAGCTTGC	29116
rs538616756	in-del	-/T			upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128288	AGTTTTCTTTTTCTC[-/T]TTTTTTTTTCTTTTT	29116
rs538649615	snp	C/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16131124	CTCTGCCTCAGCAGT[C/G]TTACTATAGGTCATT	29116
rs538787981	snp	C/T			synonymous-codon, utr-variant-5-prime	MYLIP	GRCh38.p7	6:16143080	AGCTGAATACCAAGT[C/T]TTGCAGATTGTGTCG	29116
rs539262072	snp	A/G	3.41758e-05	0.00413361	intron-variant	MYLIP	GRCh38.p7	6:16142992	AATATCTGTATACTT[A/G]ATTCTCTGTCCTCTT	29116
rs539318928	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16133572	GTGAAACAAATTAAT[A/G]TATTCTGGAAGTAGA	29116
rs539538150	snp	C/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16133977	AGTTTGACTCTGACT[C/T]GTCCCTTGTTAAATC	29116
rs539569307	snp	C/T			intron-variant	MYLIP	GRCh38.p7	6:16130072	AGGAAAACGCTGTGC[C/T]CTCAACCCCTCTAGC	29116
rs539685842	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16142446	GTTATCTATTCCTGC[A/G]TAACAAGTTACCCCA	29116
rs540147398	snp	G/T			intron-variant	MYLIP	GRCh38.p7	6:16132106	GTCCTATTATGATTT[G/T]GTAATTATTTCAAGA	29116
rs540233838	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16127888	TAGACCTTTAATAGC[C/T]AATATTGCAGTAATG	29116
rs540319288	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16144587	AACCTAAAAGCCAAG[A/G]CTTCAGGCAGATGCC	29116
rs540489374	snp	A/T	0.00119737	0.0244387	intron-variant	MYLIP	GRCh38.p7	6:16129801	ACCCGCGTGCCAGGA[A/T]GGGATGGAGTGGCTC	29116
rs540524739	snp	A/G	0.00676609	0.0577691	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128095	TTGATTCAGCAGAAC[A/G]AGTAAGGAGAAGCCC	29116
rs540550791	snp	A/C	0.000798403	0.0199641	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16129063	GGCCGCTATATCAGC[A/C]GAGTCCCTGTCGCAG	29116
rs540949620	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16138492	TATCCTCTGTCTTGG[A/G]AAGAGCCTATTAGAG	29116
rs541005234	snp	C/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16146078	TGTGTCCTTTCCCCA[C/G]AAGCAGTCATAGGCT	29116
rs541236307	snp	A/C			utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16147367	CAGTGTGGCTAGTAA[A/C]AAGCAGCTCACTCAA	29116
rs541565430	snp	C/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16132005	ATTATTATTTAAAGC[C/T]GATTTGTGAAAGCTT	29116
rs541642474	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16147921	AGGTTTTCTGGGATG[C/T]CGGGAGACCTAGATG	29116
rs542069434	snp	C/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16136860	CTTTTTCAAAGTGTC[C/G]AAGTCATTTACTCAT	29116
rs542662871	snp	C/T	0.00159617	0.0282053	intron-variant	MYLIP	GRCh38.p7	6:16129886	CGCTGCTTCTCAGGC[C/T]GCTGCTCTCAAATGC	29116
rs542693379	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128807	CGCCTGGAGCCCCGG[A/G]CGATCGCTCACTCTG	29116
rs542756800	snp	C/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16137609	GTAACTGAGAGGAAC[C/T]CTCTATGATGAGCAG	29116
rs542757172	snp	A/G			intron-variant	MYLIP	GRCh38.p7	6:16139219	CATCCTGGCTAACAC[A/G]GTGAAACCCCGTCTC	29116
rs542839558	snp	C/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16144657	CCTGGGGAGGAGGTA[C/T]GTGCTCACTGCCCTC	29116
rs543018332	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16139477	CAAGTCTTTCAGAGC[A/G]TAATTTCTTCTTTAA	29116
rs543098098	snp	A/C			intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16141467	TTTTGATTTTGCCTT[A/C]ATACTGATGATTTTT	29116
rs543344218	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140509	GGCACTTAAGAAGTC[A/G]TACATAATATACATG	29116
rs543355473	snp	C/T	8.23676e-05	0.00641693	synonymous-codon, intron-variant	MYLIP	GRCh38.p7	6:16130655	CCTGAGAAACCGGAT[C/T]TCCCAGCAGATGGAT	29116
rs543598496	snp	A/G	0.00318978	0.0398085	intron-variant	MYLIP	GRCh38.p7	6:16133693	CCAGAGATTAGAGAA[A/G]TATATGCTTCATCTT	29116
rs543872782	snp	A/C	0.00159617	0.0282053	intron-variant	MYLIP	GRCh38.p7	6:16135759	TATACATATATCTAT[A/C]TATATATATATATAT	29116
rs543944715	snp	C/T	0.000798403	0.0199641	intron-variant	MYLIP	GRCh38.p7	6:16144417	CAATATTGATTCCCT[C/T]ATTTCAGAGGGTACT	29116
rs544085202	snp	A/G	0.000798403	0.0199641	downstream-variant-500B, intron-variant	MYLIP	GRCh38.p7	6:16148741	AGCAGTAAGGGCCTC[A/G]GGCTACAGAAGCTCG	29116
rs544194779	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16144053	TTTTACCCACAGAAG[A/G]TGCATGTGTGTGAGC	29116
rs544355645	snp	G/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16142639	TGACTCCTGTGGTTT[G/T]TTGGCCTACCTCCTT	29116
rs544469607	snp	C/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16137802	AAAGAGAGAAAATTT[C/G]AAGTACTTTGAAAGA	29116
rs544482446	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128898	CAGCACTCGGCGCCC[G/T]CAAGCTGCCACCTCC	29116
rs544973629	snp	C/T			intron-variant	MYLIP	GRCh38.p7	6:16138801	GAAAGCTGATGTTGA[C/T]AGTAAGGAGAAGGAT	29116
rs545135600	snp	A/C	0.00119737	0.0244387	intron-variant	MYLIP	GRCh38.p7	6:16129638	CCCCAGCGCTGAGGG[A/C]CGGGCGCAGCCCGCA	29116
rs545180609	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16145860	TTTTAATATTAACAC[A/G]AAAAAGAGAACTCAC	29116
rs545255115	snp	C/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16145468	TGGTGACCTAAAAGG[C/T]ATTGCCCTTTAGAAA	29116
rs545486811	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16130824	TGCACCTTCCCAGAG[A/G]TACTCACAGGCAAGT	29116
rs545486894	snp	G/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140311	TCAGAGTTTTGGGCA[G/T]TGTGACCAGTATCTG	29116
rs545717521	snp	C/T	0.000798403	0.0199641	intron-variant	MYLIP	GRCh38.p7	6:16133290	ATTGCTTTTGTGTCC[C/T]CTTTATATTATTTTC	29116
rs545721389	snp	C/T	1.65048e-05	0.00287265	missense, downstream-variant-500B, utr-variant-5-prime	MYLIP, MIR4639	GRCh38.p7	6:16141710	GTGGAACTCAGTGCC[C/T]TCCTGGCCCAGACCA	29116
rs545836670	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16147753	TGTTTTTGGGGGGGG[A/G]GTTTTGTTGTGTTTT	29116
rs545925561	snp	A/G			intron-variant	MYLIP	GRCh38.p7	6:16131158	GACTGTTCTAACAGA[A/G]AGCAGGAAACAGTTC	29116
rs545991201	snp	C/G			upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128639	GCCACCATGCCCGGA[C/G]GAGAACAGTTTTCTT	29116
rs546017839	snp	C/G			intron-variant	MYLIP	GRCh38.p7	6:16133105	ATGATGGGCAGGAAG[C/G]CCTGTTTGTCATAGG	29116
rs546539224	snp	A/C			utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16147501	CAAGTACTCCCCGGG[A/C]CTTCTGAGCTGGTGG	29116
rs547137277	snp	C/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16144745	TAATCACTGAGAATA[C/T]TTACCAGACGTAAAA	29116
rs547687308	snp	A/C	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16130317	TACTTTTGAGGACTC[A/C]TTTTTTCTCTATTGC	29116
rs547796919	snp	C/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16146508	TTTCAACCTGTGAGA[C/T]GGCAAAGATCTCTAC	29116
rs548070767	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16147282	TTGATCAAGAATGAT[C/T]GGAAGGCAAACAGGT	29116
rs548107375	snp	C/T	0.00716266	0.059414	utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16147376	TAGTAAAAAGCAGCT[C/T]ACTCAATGTGGGTGG	29116
rs548274474	snp	A/C			intron-variant	MYLIP	GRCh38.p7	6:16142742	CAATATGTAAATTTG[A/C]CTTATGTATATTTTT	29116
rs548552961	snp	A/G	0.000399281	0.0141238	downstream-variant-500B, intron-variant	MYLIP	GRCh38.p7	6:16148388	TTCGGTGCTCTACAA[A/G]TTCAGAGAAACTTCT	29116
rs548623132	snp	A/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	MYLIP, MIR4639	GRCh38.p7	6:16142123	GGCAGCATCAGGGCT[A/T]CTGCATATATTCATA	29116
rs548811610	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16127243	TCATTAAGCAGTGAA[A/G]GCACTGAACTTATAG	29116
rs548902205	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16137312	GTGGTTAAGTGACTC[A/G]TTGGACTGAGGCAGG	29116
rs549256363	snp	G/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16144138	TAGACACAAAGTGTG[G/T]TAGGAGATTTCTATG	29116
rs549317876	snp	A/G	0.000181197	0.00951659	synonymous-codon, intron-variant	MYLIP	GRCh38.p7	6:16143774	CACCAAGGAATCTGG[A/G]AACAGCATCGTGCTC	29116
rs549390138	snp	C/G			intron-variant	MYLIP	GRCh38.p7	6:16133447	TGCTCTTGAATATGA[C/G]CCTCAAATGTAAAAG	29116
rs549427589	snp	A/G	0.00119737	0.0244387	utr-variant-5-prime, upstream-variant-2KB	MYLIP	GRCh38.p7	6:16129133	AGGACAGGGGCAGCT[A/G]GCGGGCAGCGGGTGA	29116
rs549483253	snp	C/T	0.000798403	0.0199641	intron-variant	MYLIP	GRCh38.p7	6:16145399	AGCCAGGTACTGGCT[C/T]GCTAATGCACAGACG	29116
rs549487189	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16138118	ATGCTCATAGGATGT[A/G]TTCATGGACATTTCC	29116
rs549565728	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16139200	GAGGTCAGGAGATTG[A/G]GACCATCCTGGCTAA	29116
rs550341101	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16133542	TGTTTGTGATGCCAT[A/G]GAATAAAATGAATAG	29116
rs550480572	snp	A/G			intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16139747	TCAGTTTAGCAGTAT[A/G]TCAGAAATACTTTAA	29116
rs550534557	in-del	-/A			intron-variant	MYLIP	GRCh38.p7	6:16132559	TAACTTGCTTTTAAT[-/A]TGTTGGTGAATTTTA	29116
rs550543587	snp	C/G			intron-variant	MYLIP	GRCh38.p7	6:16137089	CCTGAGAAACCTTTG[C/G]TACCTGGAAGTCATG	29116
rs550675758	snp	G/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16142914	ATAAGTTTTAAGTTG[G/T]TGTGATTCATCAGTG	29116
rs551020575	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16127464	GTTGTTGTTTAGAGA[C/T]AGGGTCTTTTGCTCT	29116
rs551223245	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128201	ATTTTGTTTTTCTCA[A/G]TGATGAGGTCTTAAT	29116
rs551279986	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime	MYLIP	GRCh38.p7	6:16129258	CTGGGTCCCACCAGT[A/G]ACAAGGCGGCAGCCC	29116
rs551504509	snp	G/T			intron-variant	MYLIP	GRCh38.p7	6:16132947	GGTGCATGTAGTGTA[G/T]TATACTGAAAGTATC	29116
rs551657144	snp	C/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16138159	GAAAACAGTTTTTTT[C/T]CAAAGGCTTTCTTTC	29116
rs551745362	snp	C/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16132156	TTTGATGGCACAAAA[C/T]TATTTTTTAAATCTT	29116
rs551881707	snp	G/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16130003	TCCTTAACAGTGAGG[G/T]AGATCGGTGCCAAAT	29116
rs552608958	snp	A/C	0.000399281	0.0141238	intron-variant, downstream-variant-500B	MYLIP, MIR4639	GRCh38.p7	6:16141984	ATGTTATGTCAAATA[A/C]TGTACCAGAGGAATA	29116
rs552746680	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16135537	GGTAATTATTTGGCT[A/G]TGACAAGTTTCTCAG	29116
rs552810137	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16134509	CATGTGTTTATTGTG[A/G]CTATTAGTTCTTTCC	29116
rs552856627	snp	A/C	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16134064	CTTGCTTGGGAGACT[A/C]AACTCCCCCAAGACA	29116
rs553015151	snp	A/G	0.00119737	0.0244387	intron-variant	MYLIP	GRCh38.p7	6:16142477	AAACTTAGTGACATA[A/G]AACAACAAAAATTGT	29116
rs553194436	snp	C/T	3.72349e-05	0.00431464	missense, utr-variant-5-prime	MYLIP	GRCh38.p7	6:16143028	CCTCCAGCATTGTTG[C/T]AAAACATAAGGAGTT	29116
rs553792495	snp	A/G	0.000798403	0.0199641	intron-variant	MYLIP	GRCh38.p7	6:16137511	TAAATTTTGAGTTCA[A/G]TAATGAATCTGGATA	29116
rs553822291	snp	C/T			intron-variant	MYLIP	GRCh38.p7	6:16143935	ACAACCAGGTTTCTA[C/T]GGTTCCTTGGATTGT	29116
rs553855859	snp	C/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16144310	ACTGGGCCTGCTCCA[C/T]TGCTCAGGAGAAGGA	29116
rs553941106	snp	G/T	0.000798403	0.0199641	intron-variant	MYLIP	GRCh38.p7	6:16131393	TTATCTCTCTACGTT[G/T]TAAAACACCACCAAC	29116
rs554388488	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16147569	CTTGGGAAGGGAAAG[C/T]GGAGCTTGCTGAGTG	29116
rs554970624	snp	A/T	0.00119737	0.0244387	intron-variant	MYLIP	GRCh38.p7	6:16144284	GATTACCCTAAAGGT[A/T]ACCCTGAGGGACTGG	29116
rs555066722	snp	A/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16132911	GAAAGGTGATTTTTT[A/T]ATTCTTTTCTAAATC	29116
rs555298307	snp	C/T			intron-variant	MYLIP	GRCh38.p7	6:16134196	TAAACAGGGAGCTTA[C/T]CAACATTGTATCCCC	29116
rs555383565	snp	C/T	0.000798403	0.0199641	intron-variant	MYLIP	GRCh38.p7	6:16142585	GGTAGAACTCTGTCT[C/T]ATCTGAAGGCTCGAC	29116
rs555394745	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16135714	TTACAGGGAACACCT[A/G]TGTATATATACACAC	29116
rs555534053	snp	A/C/T	0.000399281	0.0141238	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16127651	GGTTTCGCTGTGTTG[A/C/T]GAAACCGGGCTGGTC	29116
rs555584161	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16144398	TGGAAGGATTTTTTA[A/G]TAGCAATATTGATTC	29116
rs555595287	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16136653	TTATAACTAACTGCC[A/G]GACCTTTTCCCAAAG	29116
rs555660223	snp	A/G	0.000798403	0.0199641	intron-variant	MYLIP	GRCh38.p7	6:16137639	GATGAACAACTTCCA[A/G]TTGGTTTGCAGGAAG	29116
rs555964533	snp	G/T			intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16141190	ATTCTTAGGACAGAA[G/T]CTGGCACTGAGACTA	29116
rs556002452	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128828	GCTCACTCTGAGCAG[C/T]GTCGCCCAGCGGACA	29116
rs556070545	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16138509	AGAGCCTATTAGAGT[A/G]CTGATCTTTGCTACT	29116
rs556177484	snp	C/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16129575	CGTGGGGCGCGCGGT[C/T]TCCTCCTGGCGCGCG	29116
rs556503375	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16147646	CTTCTCCCAAGCACT[C/G]GATCCCAGCTTCACC	29116
rs556533262	snp	C/G	0.000798403	0.0199641	intron-variant	MYLIP	GRCh38.p7	6:16132475	ACATACCTAGTTCAA[C/G]TAGGTAATTTTAATT	29116
rs556636425	snp	A/G	0.00358779	0.0422022	intron-variant	MYLIP	GRCh38.p7	6:16139494	AATTTCTTCTTTAAC[A/G]AAAGCATAGATGCAG	29116
rs556717178	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16142277	TTTTATTTGAAAAAT[A/G]TGTAAACACAATATG	29116
rs556908068	snp	A/G			intron-variant	MYLIP	GRCh38.p7	6:16137563	TAAAAGCTCTTAAAA[A/G]TGGTGTAACTGGTGA	29116
rs556914480	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140762	CTGGGGCCAGATGGC[A/G]GAGACTCCTCAGCTC	29116
rs557046125	snp	C/G	0.00119737	0.0244387	utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16147895	GGCATTTTGGAAGCT[C/G]GTCAGCTAGCAGGTT	29116
rs557053073	snp	C/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16134300	TTAACTGATAACTAC[C/T]AATATAAGCTTTCCT	29116
rs557094698	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16133695	AGAGATTAGAGAAGT[A/G]TATGCTTCATCTTCA	29116
rs557762865	snp	G/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16136709	ACTCCCAGCAAGAAT[G/T]TAAGAGTCTAGTTCC	29116
rs557776130	snp	G/T			intron-variant	MYLIP	GRCh38.p7	6:16136708	TACTCCCAGCAAGAA[G/T]GTAAGAGTCTAGTTC	29116
rs557781119	snp	C/T	0.00159617	0.0282053	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16127809	GCTCCTATAAAGAAA[C/T]CAAAAAGGTAGGCTA	29116
rs557908911	snp	C/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16129667	CAGCCGGGATCCACC[C/T]CCCAGCGCCCCATCA	29116
rs557964319	snp	G/T			utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16147726	TAAGTATTTAGATAT[G/T]GTGTCCTTTTCTGTT	29116
rs558096963	snp	A/G	0.00993419	0.0697739	intron-variant	MYLIP	GRCh38.p7	6:16137361	GGGTTCTGACAAGGT[A/G]AGAGCAGAACCAGCC	29116
rs558244600	snp	A/C	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16130467	ATTGAACTTTGTAAA[A/C]AGCACCAGCAATCTT	29116
rs558275439	in-del	-/T			intron-variant	MYLIP	GRCh38.p7	6:16137257	ATTTGATAGCTTTTA[-/T]AATATAACTTGGCAG	29116
rs558429708	snp	G/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16144878	GGTGTTAAAGTAGAT[G/T]TTCAATCTTGCCTTG	29116
rs558704162	snp	C/T	0.000214381	0.0103511	missense, intron-variant	MYLIP	GRCh38.p7	6:16146681	GTCCCGTCTGCAGGT[C/T]GCGTGTGGAGCATGT	29116
rs558807326	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16147381	AAAAGCAGCTCACTC[A/T]ATGTGGGTGGCTCCC	29116
rs559054134	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140895	GGCTGCCTGCATGGA[G/T]TCTGGAGGAGGAGAG	29116
rs559118303	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140320	TGGGCAGTGTGACCA[C/G]TATCTGAATTTTACA	29116
rs559126255	snp	C/T			utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16147220	TTTTTAATAGGAAAG[C/T]CTTTTGTAAATTGTT	29116
rs559133571	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16141062	TGGTCTCCATTCGGA[C/G]AAAAAGGGCTTGGGA	29116
rs559286669	snp	C/T	6.7175e-05	0.00579508	missense, downstream-variant-500B, utr-variant-5-prime	MYLIP, MIR4639	GRCh38.p7	6:16141801	AGCTCTCCTCTGCCA[C/T]CTTGAACAGGTGAGG	29116
rs559405014	snp	G/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16145453	AAGGGTCTTTGTATT[G/T]GGTGACCTAAAAGGC	29116
rs559804242	snp	A/C	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16142798	TCATCACCCATCCAG[A/C]ATCCCCAAAGTGTTT	29116
rs560032393	snp	A/G	0.00159617	0.0282053	intron-variant	MYLIP	GRCh38.p7	6:16135219	TGGCTGATCTATATT[A/G]TTGGGAAAGAGATTG	29116
rs560059698	snp	C/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16144122	TCTTATGCCATTAAT[C/T]TAGACACAAAGTGTG	29116
rs560082127	snp	C/T			intron-variant	MYLIP	GRCh38.p7	6:16142286	AAAAATATGTAAACA[C/T]AATATGAAATGCTAT	29116
rs560148994	snp	A/C			intron-variant	MYLIP	GRCh38.p7	6:16131895	ATGGTATATTGAGTT[A/C]TTGGTACTCCTGAAA	29116
rs560308730	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16127206	TGGGACTCGTGAAGG[A/G]GGGTAGGGACAGGAA	29116
rs560515580	snp	C/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16146097	CAGTCATAGGCTTGT[C/G]TTTTTCTGCCCACCT	29116
rs560579860	snp	C/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16137985	CCTTGGGCCCCAAAA[C/T]GTGATCCATATATTG	29116
rs560641260	snp	A/C	0.000798403	0.0199641	intron-variant	MYLIP	GRCh38.p7	6:16144616	CCCTTTTTCTTCCAT[A/C]AGCAACTTCACTCAG	29116
rs560855721	snp	C/T	0.00279162	0.0372561	utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16146848	GTAATTATTCCAACA[C/T]CCATCTGCCATGCGA	29116
rs560909230	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16132006	TTATTATTTAAAGCC[A/G]ATTTGTGAAAGCTTT	29116
rs561241426	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140042	CCTCACTGCCTCCTC[C/T]TTAGTCGATTCTTAC	29116
rs561261371	snp	A/C			intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16141474	TTTGCCTTAATACTG[A/C]TGATTTTTTTTTGAA	29116
rs561498981	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16141296	CCATGTCAAGATACA[A/T]TTTTTCTGATTAAAA	29116
rs561570341	snp	G/T	0.000798403	0.0199641	intron-variant	MYLIP	GRCh38.p7	6:16133896	GTCCCAGACTAAATG[G/T]TCACAGAAATGCTCT	29116
rs561634825	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	MYLIP, MIR4639	GRCh38.p7	6:16141864	AGGCTTAAACAGGAT[A/G]AAACTAAGGTTGGAA	29116
rs561714482	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16143559	TTACAATAAGGCAGC[A/G]TTATGGTGATGTGAT	29116
rs561747106	snp	A/C	0.000881219	0.0209722	intron-variant	MYLIP	GRCh38.p7	6:16142982	CTCTAAAGCTAATAT[A/C]TGTATACTTAATTCT	29116
rs561826523	in-del	-/G	0.00676609	0.0577691	intron-variant	MYLIP	GRCh38.p7	6:16144551	ATTGTGAAACAGGAT[-/G]GGAAATTTTTAGACA	29116
rs561932524	snp	C/T			upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128982	GGGCGCCGCTATTGG[C/T]TGATCGGGCGGGGGA	29116
rs562047496	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16144037	TATTAATGTAGTCTT[A/G]TTTTACCCACAGAAG	29116
rs562187854	snp	C/G	0.000798403	0.0199641	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16127336	TCCCAACAATGCTGG[C/G]TGGAGACAGAGCAGA	29116
rs562229386	snp	A/G			intron-variant	MYLIP	GRCh38.p7	6:16132833	ATACTTATATAAAAT[A/G]CCATGAATATAAAAT	29116
rs562560334	snp	A/G			intron-variant	MYLIP	GRCh38.p7	6:16132681	AATTAGGACATCAGA[A/G]GCTGTACTGGGTCCA	29116
rs562602194	snp	A/G			intron-variant	MYLIP	GRCh38.p7	6:16133771	TCCCGACTTAGCCAC[A/G]TTTTAGCAGAGCTCT	29116
rs562721626	snp	A/G	1.64751e-05	0.00287007	synonymous-codon, intron-variant	MYLIP	GRCh38.p7	6:16130673	CCAGCAGATGGATGG[A/G]CTAGCCCCTTACAGG	29116
rs562938716	snp	C/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16129895	TCAGGCTGCTGCTCT[C/T]AAATGCACCGTTCAC	29116
rs562970331	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16146940	CATGCGTAGAATCAA[A/C]AACTCCAGTCATGGG	29116
rs563244948	snp	A/C	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16141012	AGAGAGAAGAAAGTC[A/C]AGTGAAATAGGACAA	29116
rs563836649	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16142666	CCTTCCCTGGCCACA[A/G]GGGCCTCAGGGGTCA	29116
rs564111147	snp	A/C	0.00318978	0.0398085	intron-variant	MYLIP	GRCh38.p7	6:16135763	CATATATCTATATAT[A/C]TATATATATATATAT	29116
rs564184524	snp	A/G			intron-variant	MYLIP	GRCh38.p7	6:16138333	TACAAAAAAAAAAAG[A/G]AGGGGGCAAAACCCA	29116
rs564227463	snp	C/G			intron-variant	MYLIP	GRCh38.p7	6:16131168	ACAGAAAGCAGGAAA[C/G]AGTTCCTCTTGGGTT	29116
rs564252332	snp	A/G	0.00119737	0.0244387	intron-variant	MYLIP	GRCh38.p7	6:16143624	TCATGAGCAAATGGG[A/G]ATCCCACAAAGGCAC	29116
rs564288385	snp	C/T			upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128716	GCGTGCTCAGAGTGA[C/T]CCAAGATATTTGAAG	29116
rs564378745	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128920	GCCACCTCCCGGGGC[A/G]GCCAGGGAAACTCAG	29116
rs564462492	snp	A/G	0.000798403	0.0199641	intron-variant	MYLIP	GRCh38.p7	6:16137900	TTAAAAAAAAAATCT[A/G]TAATGCTCAGTAAAT	29116
rs564648085	snp	C/T	0.00358779	0.0422022	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128237	ACAACAATTCTGCCT[C/T]CAAGCAACCCACTGT	29116
rs564667989	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16147922	GGTTTTCTGGGATGT[C/T]GGGAGACCTAGATGA	29116
rs564842739	in-del	-/C	0.000798403	0.0199641	intron-variant	MYLIP	GRCh38.p7	6:16129684	CCAGCGCCCCATCAT[-/C]CCCCCAACCCAGCAC	29116
rs564982445	snp	C/T	0.00119737	0.0244387	intron-variant	MYLIP	GRCh38.p7	6:16145879	AAGAGAACTCACATA[C/T]AGTTTTCTTCCTTTC	29116
rs565060423	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16139846	ATGATTTCTTTACAC[A/G]GGCTTTGAAAAAAAG	29116
rs565060432	snp	C/T			intron-variant	MYLIP	GRCh38.p7	6:16145920	AAGAATTTTAAATTT[C/T]CTCTTACAAGTTTTT	29116
rs565119605	snp	C/T			downstream-variant-500B, intron-variant	MYLIP	GRCh38.p7	6:16148602	ATGAAAAGAAAAAAT[C/T]AGGACAAGTACTGGA	29116
rs565194272	snp	C/T	1.65669e-05	0.00287805	synonymous-codon	MYLIP	GRCh38.p7	6:16145230	GGAAGCCATGCTGTG[C/T]ATGGTGTGCTGCGAG	29116
rs565435178	snp	A/G			intron-variant	MYLIP	GRCh38.p7	6:16144650	CGTCTGTCCTGGGGA[A/G]GAGGTACGTGCTCAC	29116
rs565444720	snp	C/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16131230	GTCAGATTACAGTGT[C/G]CAGCCAAGAGCTCTG	29116
rs565448190	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16147084	AGTTGGGTACCTTTT[A/G]GGAAATGATGTTGTA	29116
rs565497429	snp	A/G			missense, downstream-variant-500B, utr-variant-5-prime	MYLIP, MIR4639	GRCh38.p7	6:16141722	GCCCTCCTGGCCCAG[A/G]CCAAGTTTGGAGACT	29116
rs565606113	snp	C/T			intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16139888	GTATTTGGCAGAGTT[C/T]CATCATTTTAAATAT	29116
rs565728390	snp	C/T			intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140048	TGCCTCCTCCTTAGT[C/T]GATTCTTACCTTGCT	29116
rs565775977	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140651	ACCAGAGACACCAGA[A/G]CATGAACATGCTTCC	29116
rs565878028	snp	C/T			utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16147983	AGCTAGAAACCTACA[C/T]TGTCACTTTACTGAG	29116
rs565972770	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16141407	TGTTAAATAAGTTTA[A/T]CTTGTTTGGGTCACA	29116
rs566050622	snp	C/T	0.000798403	0.0199641	intron-variant	MYLIP	GRCh38.p7	6:16133601	GATCTGAAATAATAA[C/T]CATCTTGGAAATTCT	29116
rs566537328	snp	A/G			intron-variant	MYLIP	GRCh38.p7	6:16137892	TCACTCCATTAAAAA[A/G]AAAATCTATAATGCT	29116
rs566573243	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128397	GTGCAGTGACACAAT[C/G]TCAGCTCACTGCAAC	29116
rs566626129	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16136482	TTTATCCGTACTCCT[A/G]ATAATGAACACCTGT	29116
rs566688451	snp	A/G/T	4.94233e-05	0.00497087	missense, intron-variant	MYLIP	GRCh38.p7	6:16143743	CCCAGTCAGGAAAGA[A/G/T]TGTATATTTGACGGT	29116
rs566710895	snp	C/T			intron-variant	MYLIP	GRCh38.p7	6:16133177	CAGCTCTGCCACCAA[C/T]TACCAGCCATCCAGA	29116
rs566783364	in-del	-/T	0.00993419	0.0697739	intron-variant	MYLIP	GRCh38.p7	6:16131755	ACATTTGCTTGTTTG[-/T]TTTACCAAAGGACTG	29116
rs566859614	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16137205	TTTACTGAAATTAAA[A/G]ATACAAAACAGAAAA	29116
rs567180995	snp	A/G	0.000798403	0.0199641	intron-variant	MYLIP	GRCh38.p7	6:16145374	ATCCCTCCTCTTAAC[A/G]GGGAGTAGGAGCCAG	29116
rs567237212	snp	A/C	0.000798403	0.0199641	intron-variant	MYLIP	GRCh38.p7	6:16129560	CCTCCTCTCCACGGG[A/C]GTGGGGCGCGCGGTC	29116
rs567348383	snp	C/T	0.000798403	0.0199641	intron-variant	MYLIP	GRCh38.p7	6:16144790	TTTCATACATGCAGA[C/T]GAGACTATGAAACAT	29116
rs567571670	snp	C/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16130324	GAGGACTCCTTTTTT[C/T]TCTATTGCAATTGGT	29116
rs567726820	snp	C/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16132387	ACTTGAATCAAATTT[C/T]CTGTCTTGGTCTCTC	29116
rs567791992	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140710	CTATCCTGGGGCATA[A/G]CAGCTGCAGGGAATG	29116
rs567929267	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16148178	AAAATAATGTTTCCA[C/T]GTAAAGAACTCTGTT	29116
rs567940281	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140214	GTTATGACAAGTCAT[C/T]GAAGGAAGGTTAAAA	29116
rs568153297	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16133496	AGCTGGCATATTTCA[A/G]AGATGGAGACAGCAG	29116
rs568388430	snp	G/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16134225	CCAGAGTCTAATAAG[G/T]GTCTGTTGCATATTT	29116
rs568416480	snp	G/T	0.000798403	0.0199641	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16127124	GGGAGGATCCCTCCT[G/T]TTTTTTTAGCCTTGG	29116
rs568843193	in-del	-/A	0.00119737	0.0244387	intron-variant	MYLIP	GRCh38.p7	6:16131673	TTTGCCATGCATATG[-/A]AAAATGTGATTCTAA	29116
rs568930709	in-del	-/T	0.00119737	0.0244387	utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16148096	ATATTAAAACTCTAC[-/T]TTTTTTATGGCACAT	29116
rs568996918	snp	A/T	0.000798403	0.0199641	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128565	CAGGCTGGTCTCGAA[A/T]CTGACCTCAGGTGAT	29116
rs569041222	snp	C/T			intron-variant	MYLIP	GRCh38.p7	6:16129500	TGGCGCGCCCCCTAC[C/T]AGGGGCCGGGAGGCA	29116
rs569048306	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16136671	CCTTTTCCCAAAGCT[A/G]TTTGGCAACTGTGCT	29116
rs569058321	snp	G/T	0.000798403	0.0199641	intron-variant	MYLIP	GRCh38.p7	6:16137322	GACTCATTGGACTGA[G/T]GCAGGCTGGCTGATG	29116
rs569061086	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16145417	TAATGCACAGACGGG[A/G]AATGCCCATCTTCAC	29116
rs569164334	snp	A/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16144159	GATTTCTATGCCTAT[A/T]TAATCAATACAACAA	29116
rs569336184	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140084	TCCTCTACCTGGAAT[A/G]TCAGACACAGATATA	29116
rs569401201	snp	A/C	0.000798403	0.0199641	intron-variant	MYLIP	GRCh38.p7	6:16139224	TGGCTAACACGGTGA[A/C]ACCCCGTCTCTAATA	29116
rs569504103	snp	A/T			intron-variant	MYLIP	GRCh38.p7	6:16130253	ATTCCGGTGATTGGA[A/T]TACGAAGGAAAATAC	29116
rs569515690	snp	C/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16131114	CGATAGTAACCTCTG[C/T]CTCAGCAGTGTTACT	29116
rs569760048	snp	A/G	0.000165121	0.00908478	missense, utr-variant-5-prime	MYLIP	GRCh38.p7	6:16143030	TCCAGCATTGTTGCA[A/G]AACATAAGGAGTTGG	29116
rs570059586	snp	C/G	0.000798403	0.0199641	downstream-variant-500B, intron-variant	MYLIP	GRCh38.p7	6:16148505	TTCTAATGGAGATCA[C/G]TTCACCAGGTTATTC	29116
rs570310856	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16133570	TAGTGAAACAAATTA[A/G]TGTATTCTGGAAGTA	29116
rs570337504	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16132519	TTTGAAATTGTATGG[A/G]AAAGTTAAGTGTGAC	29116
rs570348995	snp	A/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16142387	ATTGGTGTTTTCTTC[A/T]TCCCAGCAAGAATTA	29116
rs570374762	snp	C/T	0	0	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16141372	TTTTATGTTTTGTAA[C/T]CTTAATGTTACCGAA	29116
rs570557747	snp	C/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16136386	ACAGATTTTTTGAGA[C/T]CCATCCATATTGTCC	29116
rs571051439	snp	A/G			downstream-variant-500B, intron-variant	MYLIP	GRCh38.p7	6:16148347	CTTTCCTCCTACCGG[A/G]AATTTAATTTTTTTT	29116
rs571101237	snp	C/T			intron-variant	MYLIP	GRCh38.p7	6:16145591	AACATATCTAGTTAG[C/T]GGCTTACCTGAGGAC	29116
rs571233376	snp	A/C	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16137423	TCTCCAGGAGAAATA[A/C]AATTCAATTATTGGT	29116
rs571479665	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140130	AGTGCTGAGGACATC[A/G]CACCTGGCCAAAGTT	29116
rs572045771	snp	C/T			synonymous-codon	MYLIP	GRCh38.p7	6:16144918	CACAGTGACCAGCGC[C/T]GTGATGATGCAGTAT	29116
rs572321814	snp	C/T			upstream-variant-2KB	MYLIP	GRCh38.p7	6:16127738	ACAGGTGTGAGCCAT[C/T]GAGCTGGCCTGAAGT	29116
rs572389874	snp	A/G			intron-variant	MYLIP	GRCh38.p7	6:16143936	CAACCAGGTTTCTAC[A/G]GTTCCTTGGATTGTT	29116
rs572397086	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16141441	TTTATTCCAGAGAAA[C/T]GCAGTTCTTATTTTG	29116
rs572497730	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140898	TGCCTGCATGGAGTC[C/T]GGAGGAGGAGAGCAG	29116
rs572506356	snp	A/G	0.000798403	0.0199641	intron-variant	MYLIP	GRCh38.p7	6:16132682	ATTAGGACATCAGAA[A/G]CTGTACTGGGTCCAG	29116
rs572563822	snp	G/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16131828	TTCCACTTTGCCTTG[G/T]AATCGAGCTTTAAAG	29116
rs572765675	snp	A/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	MYLIP, MIR4639	GRCh38.p7	6:16141828	GAGGCTGTTGAATAT[A/T]GTATTGTTTACAACT	29116
rs572793416	snp	A/G	0.000798403	0.0199641	intron-variant	MYLIP	GRCh38.p7	6:16134556	TTATCTGGGCCGTCT[A/G]TGAAAGTCAGATAGT	29116
rs572938045	snp	C/T			intron-variant	MYLIP	GRCh38.p7	6:16134095	TCATGTATCTTTCCT[C/T]TATAGCATTTAATGA	29116
rs573092073	snp	C/T			downstream-variant-500B, intron-variant	MYLIP	GRCh38.p7	6:16148391	GGTGCTCTACAAATT[C/T]AGAGAAACTTCTTTA	29116
rs573401763	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16144009	TTTGTTTCCGTAGTA[A/G]CAGTGGAGTCCTTAT	29116
rs573648367	snp	G/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16137565	AAAGCTCTTAAAAAT[G/T]GTGTAACTGGTGAGG	29116
rs573992750	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16138667	CTCTCAGACATGTTT[A/G]CCCTAAAACCCCAGC	29116
rs574335021	snp	C/T			intron-variant	MYLIP	GRCh38.p7	6:16130829	CTTCCCAGAGATACT[C/T]ACAGGCAAGTTTGTT	29116
rs574429000	snp	A/G	0.00199481	0.0315187	utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16146885	AAAAAAAAAAAAGGA[A/G]GAAAAATAACACAGC	29116
rs574500274	snp	C/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16132962	GTATACTGAAAGTAT[C/T]TAGACAGTTTATTAA	29116
rs574559566	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140992	ACTGGATTTAAATAG[A/T]TTTCAGAGAGAAGAA	29116
rs574992262	in-del	-/T			utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16147416	CCTTTACGCTCCCCC[-/T]ATCCCTACCCCACAA	29116
rs575130223	snp	C/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16135758	GTATACATATATCTA[C/T]ATATATATATATATA	29116
rs575166756	snp	C/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16134744	AACAGTAAAAGCAGG[C/T]ATGTGGTTATTTCCA	29116
rs575273196	in-del	-/A			intron-variant	MYLIP	GRCh38.p7	6:16139388	GCAAGACTCCATCTC[-/A]AAAAAAAAAAAAAAG	29116
rs575376639	snp	A/G	0.00159617	0.0282053	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16127652	GTTTCGCTGTGTTGC[A/G]AAACCGGGCTGGTCT	29116
rs575410254	snp	G/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16142617	GAGGGTGGCCTCCAT[G/T]CCAGGTTGACTCCTG	29116
rs575468220	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16137770	TCCTTAACATTGTAA[A/G]AAGGAATTAATTTTT	29116
rs575488230	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128114	AAGGAGAAGCCCTTC[C/T]GGAGTGTAACACACC	29116
rs576065806	snp	A/G	0.00199481	0.0315187	intron-variant	MYLIP	GRCh38.p7	6:16129599	GCGCGCGTGGGGTGC[A/G]CGGAGAAAGCGCGCA	29116
rs576263945	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16145827	GGTTGGCTGTTATTT[A/G]TTAGCAAGTCAAACT	29116
rs576387087	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16141045	AGTCCAAAGTCAGTC[C/T]GTGGTCTCCATTCGG	29116
rs576724339	snp	A/G	1.65034e-05	0.00287253	synonymous-codon, downstream-variant-500B, utr-variant-5-prime	MYLIP, MIR4639	GRCh38.p7	6:16141697	CCCAGAGCAGGCAGT[A/G]GAACTCAGTGCCCTC	29116
rs576778479	snp	A/T			intron-variant	MYLIP	GRCh38.p7	6:16137776	ACATTGTAAGAAGGA[A/T]TTAATTTTTAAAAGA	29116
rs576838900	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140915	GAGGAGGAGAGCAGC[A/G]CAGAGAATAGTGTAA	29116
rs577111255	in-del	-/AA	0.499839	0.00898417	intron-variant	MYLIP	GRCh38.p7	6:16131030	AAGTGCTACCCCAGG[-/AA]AAAAAAAAAAAAAAA	29116
rs577343919	snp	A/G			utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16147334	TTTAAAAAGTTGACA[A/G]TGTTGTCAGATTTAA	29116
rs577472817	snp	C/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16143336	GAATGAAAGATTTCA[C/T]TTTGGTATGTACATT	29116
rs577563172	snp	A/G/T			intron-variant	MYLIP	GRCh38.p7	6:16144654	TGTCCTGGGGAGGAG[A/G/T]TACGTGCTCACTGCC	29116
rs577590889	snp	C/T			intron-variant	MYLIP	GRCh38.p7	6:16138753	AGGTTGCTTTATAGC[C/T]ATGAAACTGCAAAAT	29116
rs577598182	snp	A/G	0.00358779	0.0422022	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16127178	TCGGAAATAAAGGCC[A/G]CTAACAGATCCTTGG	29116
rs577646182	snp	A/C			intron-variant	MYLIP	GRCh38.p7	6:16131198	TACTTAAACTTGGTC[A/C]GTTTCTTCAGCCTAG	29116
rs577680996	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	MYLIP	GRCh38.p7	6:16127822	AATCAAAAAGGTAGG[C/T]TATGTAATATATTGG	29116
rs577709572	snp	C/T			intron-variant	MYLIP	GRCh38.p7	6:16136844	TTGGCCTTTCATGTA[C/T]CTTTTTCAAAGTGTC	29116
rs577745830	snp	C/T	0.000798403	0.0199641	intron-variant	MYLIP	GRCh38.p7	6:16136734	AGTTCCTCCACATCC[C/T]TGCCAGCTTTCTGGT	29116
rs577850325	snp	C/T	0.00119737	0.0244387	intron-variant	MYLIP	GRCh38.p7	6:16129676	TCCACCCCCCAGCGC[C/T]CCATCATCCCCCCAA	29116
rs577912528	snp	A/T	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16138461	TTCTTGTTGGAAACA[A/T]GTCTCTGAGCTCTGC	29116
rs577986258	snp	A/G	0.000399281	0.0141238	intron-variant	MYLIP	GRCh38.p7	6:16144516	ACTTTAAACTTTTTT[A/G]TTTTAAAATAGATAC	29116
rs745311013	snp	C/T			intron-variant	MYLIP	GRCh38.p7	6:16132206	ATAACTGCATTTAAA[C/T]AATGGCTGCAGTGAT	29116
rs745412254	snp	A/G	1.79085e-05	0.00299231	intron-variant, downstream-variant-500B	MYLIP, MIR4639	GRCh38.p7	6:16141844	GTATTGTTTACAACT[A/G]GAATAGGCTTAAACA	29116
rs745612454	snp	A/G	3.33183e-05	0.00408143	missense, utr-variant-5-prime	MYLIP	GRCh38.p7	6:16129374	ATGGAGGTGGAGGTG[A/G]AGGCGAAAGCCAACG	29116
rs745798121	snp	C/T			intron-variant	MYLIP	GRCh38.p7	6:16145924	ATTTTAAATTTCCTC[C/T]TACAAGTTTTTTCAA	29116
rs745891375	snp	C/T			intron-variant	MYLIP	GRCh38.p7	6:16136163	TTTAAATAAAACTGC[C/T]ATCAAAATTTAGAAC	29116
rs746135355	snp	A/G			intron-variant	MYLIP	GRCh38.p7	6:16137629	ATGATGAGCAGATGA[A/G]CAACTTCCAATTGGT	29116
rs746153632	snp	G/T	1.68618e-05	0.00290356	intron-variant, nc-transcript-variant	MYLIP, MIR4639	GRCh38.p7	6:16141619	CACTCTCACCTTGCT[G/T]TGCAGGCATATCTTT	29116
rs746214444	snp	C/T			intron-variant	MYLIP	GRCh38.p7	6:16144459	TTGTGATTGGACTCA[C/T]GTATTTGGACAATTA	29116
rs746273034	snp	C/T	1.64822e-05	0.00287068	missense	MYLIP	GRCh38.p7	6:16145109	ACAACCAGAGCCCTT[C/T]ACACTCGCCTCTGAA	29116
rs746798313	snp	A/G	1.64732e-05	0.0028699	missense	MYLIP	GRCh38.p7	6:16143174	ATTGGGGTTGGACCT[A/G]AAGGAATCTCAATTT	29116
rs746811748	snp	A/G	1.65176e-05	0.00287376	intron-variant	MYLIP	GRCh38.p7	6:16143257	GACCTAAGCATGTGT[A/G]TACATCTGTAGCTGT	29116
rs747045166	snp	A/G			utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16147964	GCAATACTAGCTAAG[A/G]TAAAGCTAGAAACCT	29116
rs747073422	snp	C/G	1.64936e-05	0.00287168	missense, intron-variant	MYLIP	GRCh38.p7	6:16130719	AAGTTCTTCGTGGAG[C/G]CTCATCTCATCTTAC	29116
rs747161589	snp	C/T	4.94368e-05	0.00497152	missense	MYLIP	GRCh38.p7	6:16144959	TGAAGGGCCACTTGG[C/T]ATCTCTGTTTCTGAA	29116
rs747207548	snp	C/T			upstream-variant-2KB	MYLIP	GRCh38.p7	6:16127358	CAGAGCAGATATTGC[C/T]ATCTCCATTTTACTG	29116
rs747455543	snp	C/T	1.72913e-05	0.0029403	synonymous-codon, utr-variant-5-prime	MYLIP	GRCh38.p7	6:16143042	GCAAAACATAAGGAG[C/T]TGGAGGGGACCAGCC	29116
rs747923546	snp	C/T	2.09756e-05	0.00323842	missense, intron-variant	MYLIP	GRCh38.p7	6:16146713	CAGCACGTCTATCTG[C/T]CAACGCACACCAGTC	29116
rs747981623	snp	C/T	1.64773e-05	0.00287026	missense, utr-variant-5-prime	MYLIP	GRCh38.p7	6:16143094	TTTTGCAGATTGTGT[C/T]GGCAATGGAAAACTA	29116
rs748014754	snp	G/T			upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128562	TGCCAGGCTGGTCTC[G/T]AATCTGACCTCAGGT	29116
rs748144313	snp	C/T	1.65416e-05	0.00287586	synonymous-codon, intron-variant	MYLIP	GRCh38.p7	6:16130562	TTTGTTTTAGGTGTG[C/T]AGGCGACTGGGAATC	29116
rs748155583	snp	A/C			intron-variant	MYLIP	GRCh38.p7	6:16135413	TTCCCAGCTGCTGCC[A/C]TCCACATCTTTTAAC	29116
rs748156535	snp	C/T	1.6517e-05	0.00287372	missense, intron-variant	MYLIP	GRCh38.p7	6:16143859	GAGACGCACGCATTC[C/T]ACAGGCACGTATCTC	29116
rs748173924	snp	A/G	1.64811e-05	0.00287059	missense, intron-variant	MYLIP	GRCh38.p7	6:16130704	CTTAAACTTAGAGTC[A/G]AGTTCTTCGTGGAGC	29116
rs748452132	snp	A/T			intron-variant	MYLIP	GRCh38.p7	6:16146501	TATAAACTTTCAACC[A/T]GTGAGACGGCAAAGA	29116
rs748472377	snp	C/T	1.64749e-05	0.00287005	missense, intron-variant	MYLIP	GRCh38.p7	6:16143791	ACAGCATCGTGCTCT[C/T]GTTTAAAATGATCAG	29116
rs748499615	snp	A/C	3.55967e-05	0.00421866	intron-variant, downstream-variant-500B	MYLIP, MIR4639	GRCh38.p7	6:16141840	TATAGTATTGTTTAC[A/C]ACTAGAATAGGCTTA	29116
rs748701902	snp	C/T			intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16139738	GCTCCTTTCTCAGTT[C/T]AGCAGTATGTCAGAA	29116
rs748720122	snp	A/C	1.65141e-05	0.00287346	synonymous-codon, downstream-variant-500B, utr-variant-5-prime	MYLIP, MIR4639	GRCh38.p7	6:16141724	CCTCCTGGCCCAGAC[A/C]AAGTTTGGAGACTAC	29116
rs748784154	snp	A/T	3.29457e-05	0.00405854	missense	MYLIP	GRCh38.p7	6:16143157	AAGGGCAGAAACTGC[A/T]CATTGGGGTTGGACC	29116
rs748822883	snp	A/G	1.80471e-05	0.00300387	intron-variant, downstream-variant-500B	MYLIP, MIR4639	GRCh38.p7	6:16141847	TTGTTTACAACTAGA[A/G]TAGGCTTAAACAGGA	29116
rs748880775	snp	C/T	2.06708e-05	0.0032148	missense, intron-variant	MYLIP	GRCh38.p7	6:16146692	AGGTCGCGTGTGGAG[C/T]ATGTCCAGCACGTCT	29116
rs748945573	snp	A/G			intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16141096	AATATATGGAGTTTG[A/G]TTTTGAATGAGCCAA	29116
rs748968995	snp	C/G			intron-variant, downstream-variant-500B	MYLIP, MIR4639	GRCh38.p7	6:16142043	GGTATCCAAGCAAGG[C/G]GACAGAAAGAATGGC	29116
rs748990733	snp	C/G			intron-variant	MYLIP	GRCh38.p7	6:16146327	GCATTGCTGCCTGAA[C/G]TGTTATAGTCTACTC	29116
rs749091403	snp	C/T	1.69075e-05	0.00290748	intron-variant	MYLIP	GRCh38.p7	6:16130519	TTGCTTTGATACGTA[C/T]CATTTGCTCATCCAG	29116
rs749114638	snp	C/T	3.4951e-05	0.00418022	intron-variant	MYLIP	GRCh38.p7	6:16146615	GAGACACAGGCCCCC[C/T]ACCGAGGCTTGCATG	29116
rs749160939	snp	A/G	3.30006e-05	0.00406192	missense, intron-variant	MYLIP	GRCh38.p7	6:16143853	ATAACAGAGACGCAC[A/G]CATTCTACAGGCACG	29116
rs749267007	snp	A/G			intron-variant	MYLIP	GRCh38.p7	6:16132474	TACATACCTAGTTCA[A/G]CTAGGTAATTTTAAT	29116
rs749285467	snp	C/G	5.22835e-05	0.00511263	synonymous-codon, utr-variant-5-prime	MYLIP	GRCh38.p7	6:16129385	GGTGGAGGCGAAAGC[C/G]AACGGCGAGGACTGC	29116
rs749288448	snp	A/T			utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16147725	ATAAGTATTTAGATA[A/T]GGTGTCCTTTTCTGT	29116
rs749397478	snp	A/G	1.64741e-05	0.00286998	missense, intron-variant	MYLIP	GRCh38.p7	6:16143781	GAATCTGGGAACAGC[A/G]TCGTGCTCTTGTTTA	29116
rs749605563	snp	G/T			intron-variant	MYLIP	GRCh38.p7	6:16130163	ATGTGTTTGATTTTT[G/T]GAGTCCAAATGGTTA	29116
rs749633743	snp	G/T	1.66186e-05	0.00288254	missense, downstream-variant-500B, utr-variant-5-prime	MYLIP, MIR4639	GRCh38.p7	6:16141634	TTGCAGGCATATCTT[G/T]TTCTTGCACATCAAG	29116
rs749813948	snp	C/T			utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16146857	CCAACACCCATCTGC[C/T]ATGCGATGTTAAAAA	29116
rs749830853	snp	A/G	1.6501e-05	0.00287232	missense	MYLIP	GRCh38.p7	6:16145141	TCCTCAGAAAGCAGC[A/G]TGAACTGCAGCAGCT	29116
rs749881130	snp	A/G			utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16147489	CTGTGGAGTAGTCAA[A/G]TACTCCCCGGGCCTT	29116
rs750024552	snp	A/G/T	6.97295e-05	0.0059043	intron-variant	MYLIP	GRCh38.p7	6:16144883	TAAAGTAGATGTTCA[A/G/T]TCTTGCCTTGCAGGT	29116
rs750024839	snp	A/T			intron-variant	MYLIP	GRCh38.p7	6:16134849	ATTATATGTGTTTAT[A/T]TCAGCCAAGGAACGC	29116
rs750043397	snp	C/G	1.64754e-05	0.00287009	missense, intron-variant	MYLIP	GRCh38.p7	6:16130672	CCCAGCAGATGGATG[C/G]GCTAGCCCCTTACAG	29116
rs750125997	snp	A/T			intron-variant	MYLIP	GRCh38.p7	6:16133551	TGCCATGGAATAAAA[A/T]GAATAGTGAAACAAA	29116
rs750142606	snp	A/C	8.9218e-05	0.0066784	intron-variant	MYLIP	GRCh38.p7	6:16129445	GGGGCCCCGGCGGGT[A/C]CCGCGAGGCCGAGGG	29116
rs750155367	in-del	-/GAG	7.12606e-05	0.00596869	cds-indel	MYLIP	GRCh38.p7	6:16145243	TGCATGGTGTGCTGC[-/GAG]GAGGAGATCAACTCC	29116
rs750232620	snp	G/T			intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140856	ATGACAAGTTTATAC[G/T]AGAAACAAGCAGCAT	29116
rs750254052	snp	C/T	3.29875e-05	0.00406112	missense, intron-variant	MYLIP	GRCh38.p7	6:16143848	GAGCGATAACAGAGA[C/T]GCACGCATTCTACAG	29116
rs750505428	snp	C/T	1.72187e-05	0.00293412	missense	MYLIP	GRCh38.p7	6:16145283	GTCCCTGTGGCCACA[C/T]TGTGTGCTGTGAGAG	29116
rs750549300	snp	C/T	3.3083e-05	0.00406699	missense	MYLIP	GRCh38.p7	6:16145204	CTGCAGGAGAAGCTA[C/T]GCAAGCTGAAGGAAG	29116
rs750575255	snp	A/G	3.32508e-05	0.00407729	missense, downstream-variant-500B, utr-variant-5-prime	MYLIP, MIR4639	GRCh38.p7	6:16141782	GAGGAGCTCTGTGCC[A/G]AGGAGCTCTCCTCTG	29116
rs750888802	snp	G/T	1.64999e-05	0.00287222	intron-variant	MYLIP	GRCh38.p7	6:16143242	GACTTAACTTTTTTT[G/T]ACCTAAGCATGTGTA	29116
rs751026013	snp	C/T	1.64852e-05	0.00287094	missense, intron-variant	MYLIP	GRCh38.p7	6:16143836	GCGGGCTCTACCGAG[C/T]GATAACAGAGACGCA	29116
rs751066495	snp	A/G	0.000456656	0.0151036	intron-variant	MYLIP	GRCh38.p7	6:16129431	GCGAGGGGCAAGAAG[A/G]GGCCCCGGCGGGTCC	29116
rs751119580	snp	G/T	6.15366e-05	0.00554658	synonymous-codon, utr-variant-5-prime	MYLIP	GRCh38.p7	6:16129352	GACGAGGCCGGACGC[G/T]GTGCTGATGGAGGTG	29116
rs751165545	snp	C/T	1.64746e-05	0.00287002	synonymous-codon, intron-variant	MYLIP	GRCh38.p7	6:16143744	CCAGTCAGGAAAGAA[C/T]GTATATTTGACGGTC	29116
rs751208258	snp	A/G			intron-variant	MYLIP	GRCh38.p7	6:16131827	TTTCCACTTTGCCTT[A/G]TAATCGAGCTTTAAA	29116
rs751270679	in-del	-/GT	4.10416e-05	0.0045298	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16141514	TGTTAAGCATTTTCA[-/GT]GTGACTTTTAAAATT	29116
rs751523998	snp	A/G			intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140075	TGCTCATGTTCCTCT[A/G]CCTGGAATGTCAGAC	29116
rs751544491	snp	C/G	4.97673e-05	0.00498811	missense, downstream-variant-500B, utr-variant-5-prime	MYLIP, MIR4639	GRCh38.p7	6:16141773	TATAACTATGAGGAG[C/G]TCTGTGCCAAGGAGC	29116
rs751575762	snp	A/G			intron-variant	MYLIP	GRCh38.p7	6:16138965	GGCTGCCTGCCACCT[A/G]TTTACATTCTGTTAC	29116
rs751673990	snp	A/G	1.64768e-05	0.00287021	missense	MYLIP	GRCh38.p7	6:16145096	CTCGTTTCAAGAAAC[A/G]ACCAGAGCCCTTCAC	29116
rs751792497	in-del	-/C			upstream-variant-2KB	MYLIP	GRCh38.p7	6:16128652	GACGAGAACAGTTTT[-/C]TTTAGGCTTTGGGTT	29116
rs751944966	snp	A/T	3.29457e-05	0.00405854	missense	MYLIP	GRCh38.p7	6:16143154	GCGAAGGGCAGAAAC[A/T]GCTCATTGGGGTTGG	29116
rs752095593	snp	C/T			missense	MYLIP	GRCh38.p7	6:16143160	GGCAGAAACTGCTCA[C/T]TGGGGTTGGACCTGA	29116
rs752181392	snp	A/G			intron-variant	MYLIP	GRCh38.p7	6:16138717	CGGTGCAAGACAAAT[A/G]TTTATTGGCTTGAAA	29116
rs752243778	snp	C/T	3.30218e-05	0.00406323	intron-variant	MYLIP	GRCh38.p7	6:16143250	TTTTTTTGACCTAAG[C/T]ATGTGTATACATCTG	29116
rs752296595	snp	C/G	1.64776e-05	0.00287028	missense, intron-variant	MYLIP	GRCh38.p7	6:16143732	GCAGATGGCCACCCA[C/G]TCAGGAAAGAATGTA	29116
rs752327773	snp	C/G/T	5.74762e-05	0.00536049	splice-donor-variant	MYLIP	GRCh38.p7	6:16129411	ACTGCCTCAACCAGG[C/G/T]GAGGGCGAGGGGCAA	29116
rs752488097	snp	C/G	1.65002e-05	0.00287225	missense, downstream-variant-500B, utr-variant-5-prime	MYLIP, MIR4639	GRCh38.p7	6:16141686	CTCTTGTGTTCCCCA[C/G]AGCAGGCAGTGGAAC	29116
rs752703102	in-del	-/GGC			intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140853	AAATGACAAGTTTAT[-/GGC]ACTAGAAACAAGCAG	29116
rs752705834	snp	G/T			intron-variant	MYLIP	GRCh38.p7	6:16145436	GCCCATCTTCACCCG[G/T]AAAGGGTCTTTGTAT	29116
rs752715251	snp	A/C	3.30256e-05	0.00406346	missense, downstream-variant-500B, utr-variant-5-prime	MYLIP, MIR4639	GRCh38.p7	6:16141654	TGCACATCAAGGAGG[A/C]CCTCTTGGCAGGCCA	29116
rs752855647	snp	C/T	1.65116e-05	0.00287324	missense	MYLIP	GRCh38.p7	6:16144937	ATGATGCAGTATAGC[C/T]GTGACTTGAAGGGCC	29116
rs752891296	snp	C/T			upstream-variant-2KB	MYLIP	GRCh38.p7	6:16127355	AGACAGAGCAGATAT[C/T]GCCATCTCCATTTTA	29116
rs752942314	snp	A/G			intron-variant	MYLIP	GRCh38.p7	6:16138422	GATTCAAAACCACCC[A/G]TAAATATTGAGCCAT	29116
rs752944308	snp	C/T			missense	MYLIP	GRCh38.p7	6:16143100	AGATTGTGTCGGCAA[C/T]GGAAAACTATGGCAT	29116
rs753046284	snp	C/T	8.47529e-05	0.00650917	missense, intron-variant	MYLIP	GRCh38.p7	6:16146683	CCCGTCTGCAGGTCG[C/T]GTGTGGAGCATGTCC	29116
rs753535604	snp	A/G	2.34739e-05	0.00342584	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16141552	CTTAAAAGTGACTGT[A/G]AAATTGCTAAGTAGG	29116
rs753587065	snp	A/T	1.6477e-05	0.00287024	synonymous-codon, intron-variant	MYLIP	GRCh38.p7	6:16130691	AGCCCCTTACAGGCT[A/T]AAACTTAGAGTCAAG	29116
rs753619726	snp	A/G	3.42524e-05	0.00413824	synonymous-codon	MYLIP	GRCh38.p7	6:16144897	AATCTTGCCTTGCAG[A/G]TGTGACACAGTGACC	29116
rs753916173	snp	A/T			intron-variant	MYLIP	GRCh38.p7	6:16137691	ATTGCTTTATGAGAC[A/T]AGCCTGTGTTTAGAG	29116
rs753949077	snp	C/T	5.52517e-05	0.00525574	intron-variant	MYLIP	GRCh38.p7	6:16143003	ACTTAATTCTCTGTC[C/T]TCTTGGTGTCCTCCA	29116
rs753951366	snp	A/G	1.73312e-05	0.00294369	intron-variant, downstream-variant-500B	MYLIP, MIR4639	GRCh38.p7	6:16141819	TGAACAGGTGAGGCT[A/G]TTGAATATAGTATTG	29116
rs754002036	snp	A/T	2.15334e-05	0.00328119	missense, intron-variant	MYLIP	GRCh38.p7	6:16146680	TGTCCCGTCTGCAGG[A/T]CGCGTGTGGAGCATG	29116
rs754039788	snp	A/G			intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140635	CAGAGGGAGCAGCAA[A/G]ACCAGAGACACCAGA	29116
rs754235257	snp	C/T	1.75773e-05	0.00296452	synonymous-codon	MYLIP	GRCh38.p7	6:16145299	TGTGTGCTGTGAGAG[C/T]TGCGCCGCCCAGCTA	29116
rs754325378	in-del	-/GT	1.65759e-05	0.00287883	frameshift-variant, intron-variant	MYLIP	GRCh38.p7	6:16130557	TCCTTTTTGTTTTAG[-/GT]GTGCAGGCGACTGGG	29116
rs754392132	snp	A/G	5.827e-05	0.00539737	intron-variant	MYLIP	GRCh38.p7	6:16129412	CTGCCTCAACCAGGT[A/G]AGGGCGAGGGGCAAG	29116
rs754426866	snp	C/T			intron-variant	MYLIP	GRCh38.p7	6:16131355	CAGATATGTTACACA[C/T]GATTGGTGAGTATAG	29116
rs754445121	snp	A/G	0.000316106	0.0125679	utr-variant-5-prime	MYLIP	GRCh38.p7	6:16129310	GGCTGTGGCGGCAGC[A/G]GCAGCCCCAGCCATG	29116
rs754451828	snp	A/G			intron-variant	MYLIP	GRCh38.p7	6:16137004	TTTCTGATGCCTTTT[A/G]TGAGTAGAAGTTTTT	29116
rs754492189	snp	C/T	1.6473e-05	0.00286988	synonymous-codon	MYLIP	GRCh38.p7	6:16143158	AGGGCAGAAACTGCT[C/T]ATTGGGGTTGGACCT	29116
rs754498572	snp	C/T			intron-variant	MYLIP	GRCh38.p7	6:16135048	TGTGTTTCCTCTGAA[C/T]GGTGTCCCACTGTGG	29116
rs754543202	snp	C/T	1.65031e-05	0.00287251	intron-variant	MYLIP	GRCh38.p7	6:16143245	TTAACTTTTTTTGAC[C/T]TAAGCATGTGTATAC	29116
rs754752699	snp	C/G	2.13805e-05	0.00326953	intron-variant, nc-transcript-variant	MYLIP, MIR4639	GRCh38.p7	6:16141559	GTGACTGTGAAATTG[C/G]TAAGTAGGCTGAGAT	29116
rs754805685	snp	C/T	1.64779e-05	0.00287031	missense, intron-variant	MYLIP	GRCh38.p7	6:16130695	CCTTACAGGCTTAAA[C/T]TTAGAGTCAAGTTCT	29116
rs754869754	snp	A/C	3.30038e-05	0.00406212	synonymous-codon, intron-variant	MYLIP	GRCh38.p7	6:16143855	AACAGAGACGCACGC[A/C]TTCTACAGGCACGTA	29116
rs755012758	snp	A/G			downstream-variant-500B, intron-variant	MYLIP	GRCh38.p7	6:16148736	GTCATAGCAGTAAGG[A/G]CCTCGGGCTACAGAA	29116
rs755061811	snp	A/G			intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140825	ACAGATCCTTTGAAG[A/G]ATTTTGAGCAGAGAA	29116
rs755252450	snp	C/T			intron-variant	MYLIP	GRCh38.p7	6:16135083	TTCCCAGCCCTCTTC[C/T]GTACCAGCAGCAGGA	29116
rs755258458	snp	A/C			intron-variant, nc-transcript-variant	MYLIP, MIR4639	GRCh38.p7	6:16141589	TTGATGTCAGGTTAT[A/C]CCCAAGCATAACCTC	29116
rs755361705	snp	C/T			intron-variant	MYLIP	GRCh38.p7	6:16131590	TAAAAAGGAAAACAG[C/T]TACTTTGAAGACATA	29116
rs755521818	snp	A/G	1.65671e-05	0.00287807	missense	MYLIP	GRCh38.p7	6:16145231	GAAGCCATGCTGTGC[A/G]TGGTGTGCTGCGAGG	29116
rs755597980	snp	C/T	2.08388e-05	0.00322784	missense, intron-variant	MYLIP	GRCh38.p7	6:16146687	TCTGCAGGTCGCGTG[C/T]GGAGCATGTCCAGCA	29116
rs755646615	snp	A/G			utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16147498	AGTCAAGTACTCCCC[A/G]GGCCTTCTGAGCTGG	29116
rs755651136	snp	A/G	1.6625e-05	0.00288309	missense, utr-variant-5-prime	MYLIP	GRCh38.p7	6:16143060	GAGGGGACCAGCCAG[A/G]CTTCAGCTGAATACC	29116
rs755832345	in-del	-/T			downstream-variant-500B, intron-variant	MYLIP	GRCh38.p7	6:16148444	CTTGAGAGTATAGTC[-/T]TTTTTTTTTTTTTTC	29116
rs755851987	snp	C/G	1.83199e-05	0.00302648	intron-variant	MYLIP	GRCh38.p7	6:16129455	CGGGTCCCGCGAGGC[C/G]GAGGGGCCTCGCAGC	29116
rs756060886	snp	A/G			intron-variant	MYLIP	GRCh38.p7	6:16139078	AAAACTCTTCTTACT[A/G]TCTAATAAAGCAGGA	29116
rs756090946	snp	A/G	1.64735e-05	0.00286993	synonymous-codon, intron-variant	MYLIP	GRCh38.p7	6:16143768	GACGGTCACCAAGGA[A/G]TCTGGGAACAGCATC	29116
rs756116375	snp	A/G			intron-variant	MYLIP	GRCh38.p7	6:16131155	GCAGACTGTTCTAAC[A/G]GAAAGCAGGAAACAG	29116
rs756343170	snp	A/G	6.88658e-05	0.00586755	missense	MYLIP	GRCh38.p7	6:16145285	CCCTGTGGCCACACT[A/G]TGTGCTGTGAGAGCT	29116
rs756350815	snp	C/G	4.95323e-05	0.00497631	synonymous-codon, downstream-variant-500B, utr-variant-5-prime	MYLIP, MIR4639	GRCh38.p7	6:16141718	CAGTGCCCTCCTGGC[C/G]CAGACCAAGTTTGGA	29116
rs756428899	snp	A/G			intron-variant	MYLIP	GRCh38.p7	6:16139169	GCACTTTGGGAGGCC[A/G]AGGCAGGCAGATCAT	29116
rs756471591	snp	A/G			upstream-variant-2KB	MYLIP	GRCh38.p7	6:16127593	AGACTACAGGCAGGC[A/G]CCACCACGCCTGGCT	29116
rs756594397	snp	C/G			intron-variant	MYLIP	GRCh38.p7	6:16134339	TTGAGATGTTTTTCA[C/G]TTTGCTTTTATAAAC	29116
rs756696457	snp	C/G			intron-variant	MYLIP	GRCh38.p7	6:16145813	CTCAAGGGCATATGG[C/G]TTGGCTGTTATTTAT	29116
rs756802940	snp	G/T	5.71119e-05	0.00534347	missense, utr-variant-5-prime	MYLIP	GRCh38.p7	6:16129360	CGGACGCGGTGCTGA[G/T]GGAGGTGGAGGTGGA	29116
rs756826225	snp	A/G	1.7843e-05	0.00298683	intron-variant	MYLIP	GRCh38.p7	6:16129439	CAAGAAGGGGCCCCG[A/G]CGGGTCCCGCGAGGC	29116
rs756957678	in-del	-/TG	2.53482e-05	0.00355998	intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16141549	TTCCTTAAAAGTGAC[-/TG]TGAAATTGCTAAGTA	29116
rs757090167	snp	C/T			intron-variant	MYLIP	GRCh38.p7	6:16139022	CTGTCTCTCCGGAAG[C/T]GTAGGCATGGATAGG	29116
rs757137180	snp	A/G			intron-variant	MYLIP	GRCh38.p7	6:16137464	TTGAAAAAAATAGCT[A/G]CTTAGCTGTTTTAAA	29116
rs757152660	in-del	-/TTG			intron-variant	MYLIP	GRCh38.p7	6:16136878	GTCATTTACTCATTT[-/TTG]TTGTTTGCTTTTATT	29116
rs757301617	snp	C/T			upstream-variant-2KB	MYLIP	GRCh38.p7	6:16127520	GGGATCACAGCACAC[C/T]GCAGCCTCGAACTCC	29116
rs757402245	snp	A/G	1.6504e-05	0.00287258	missense, downstream-variant-500B, utr-variant-5-prime	MYLIP, MIR4639	GRCh38.p7	6:16141704	CAGGCAGTGGAACTC[A/G]GTGCCCTCCTGGCCC	29116
rs757455261	snp	C/T	5.10425e-05	0.0050516	intron-variant, nc-transcript-variant	MYLIP, MIR4639	GRCh38.p7	6:16141613	TAACCTCACTCTCAC[C/T]TTGCTTTGCAGGCAT	29116
rs757600935	snp	C/G/T	3.29556e-05	0.00405918	missense, synonymous-codon	MYLIP	GRCh38.p7	6:16145098	CGTTTCAAGAAACAA[C/G/T]CAGAGCCCTTCACAC	29116
rs757616374	snp	A/C			intron-variant, downstream-variant-500B	MYLIP, MIR4639	GRCh38.p7	6:16141891	GGAAGGTAAACTAAT[A/C]ACACATAATATGCAG	29116
rs757758904	snp	A/G	9.88338e-05	0.00702902	synonymous-codon	MYLIP	GRCh38.p7	6:16143155	CGAAGGGCAGAAACT[A/G]CTCATTGGGGTTGGA	29116
rs757775049	snp	A/G/T	1.64732e-05	0.0028699	synonymous-codon	MYLIP	GRCh38.p7	6:16143164	GAAACTGCTCATTGG[A/G/T]GTTGGACCTGAAGGA	29116
rs757776788	snp	A/G			upstream-variant-2KB	MYLIP	GRCh38.p7	6:16127341	ACAATGCTGGGTGGA[A/G]ACAGAGCAGATATTG	29116
rs757959611	snp	G/T			intron-variant	MYLIP	GRCh38.p7	6:16144029	GGAGTCCTTATTAAT[G/T]TAGTCTTGTTTTACC	29116
rs757967085	snp	C/G	0.00199876	0.0315497	utr-variant-5-prime	MYLIP	GRCh38.p7	6:16129315	TGGCGGCAGCGGCAG[C/G]CCCAGCCATGCTGTG	29116
rs758106307	snp	G/T			intron-variant	MYLIP	GRCh38.p7	6:16135593	GATGTGGTGGTTCAC[G/T]TTAGATATGGCTAGT	29116
rs758157860	in-del	-/AAA			intron-variant	MYLIP	GRCh38.p7	6:16131030	AAGTGCTACCCCAGG[-/AAA]AAAAAAAAAAAAAAA	29116
rs758175325	snp	A/G	6.60447e-05	0.00574613	intron-variant	MYLIP	GRCh38.p7	6:16143253	TTTTGACCTAAGCAT[A/G]TGTATACATCTGTAG	29116
rs758214635	snp	C/G			intron-variant	MYLIP	GRCh38.p7	6:16145583	TCCTGGGTAACATAT[C/G]TAGTTAGCGGCTTAC	29116
rs758361762	snp	A/G	3.30066e-05	0.00406229	missense	MYLIP	GRCh38.p7	6:16144938	TGATGCAGTATAGCC[A/G]TGACTTGAAGGGCCA	29116
rs758403214	snp	A/G	1.64811e-05	0.00287059	missense, intron-variant	MYLIP	GRCh38.p7	6:16130705	TTAAACTTAGAGTCA[A/G]GTTCTTCGTGGAGCC	29116
rs758426413	snp	C/G			intron-variant	MYLIP	GRCh38.p7	6:16137327	ATTGGACTGAGGCAG[C/G]CTGGCTGATGATCAC	29116
rs758574394	in-del	-/GAA			intron-variant	MYLIP	GRCh38.p7	6:16145901	CTTCCTTTCTTGCAT[-/GAA]GAAGAATTTTAAATT	29116
rs758662535	snp	A/G			upstream-variant-2KB	MYLIP	GRCh38.p7	6:16127158	CTGATATCGTACCTG[A/G]TTGTTCGGAAATAAA	29116
rs758683274	snp	C/T			intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140853	GAAATGACAAGTTTA[C/T]ACTAGAAACAAGCAG	29116
rs758773363	snp	A/G	3.29457e-05	0.00405854	missense	MYLIP	GRCh38.p7	6:16143141	TCTGTGCGGGATAGC[A/G]AAGGGCAGAAACTGC	29116
rs758834732	snp	C/G			intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140913	TGGAGGAGGAGAGCA[C/G]CGCAGAGAATAGTGT	29116
rs758949875	snp	C/G			utr-variant-5-prime	MYLIP	GRCh38.p7	6:16129219	GCTGCAGCCTTCGAG[C/G]GCCAGCCCTCTCCGA	29116
rs759024621	snp	A/G	9.91309e-05	0.00703958	missense, downstream-variant-500B, utr-variant-5-prime	MYLIP, MIR4639	GRCh38.p7	6:16141735	AGACCAAGTTTGGAG[A/G]CTACAACCAGAACAC	29116
rs759282321	snp	C/T			intron-variant	MYLIP	GRCh38.p7	6:16143947	CTACGGTTCCTTGGA[C/T]TGTTGTGTCAATGAG	29116
rs759291263	snp	C/G			intron-variant	MYLIP	GRCh38.p7	6:16138570	CATAAACTTGTCACC[C/G]AAAAGCTAGATTGTG	29116
rs759374818	snp	A/G			missense	MYLIP	GRCh38.p7	6:16145246	ATGGTGTGCTGCGAG[A/G]AGGAGATCAACTCCA	29116
rs759437156	snp	C/G			upstream-variant-2KB	MYLIP	GRCh38.p7	6:16127875	GAGTGAAGGGTTGTA[C/G]ACCTTTAATAGCTAA	29116
rs759481620	snp	C/T			intron-variant	MYLIP	GRCh38.p7	6:16133246	CTGAAGAGATGGTTT[C/T]TAAATTTCTCTTAGC	29116
rs759555686	snp	A/G	1.64754e-05	0.00287009	missense	MYLIP	GRCh38.p7	6:16143198	TCAATTTGTAAAGAT[A/G]ACTTTAGCCCAATTA	29116
rs759630605	snp	A/G	3.29457e-05	0.00405854	missense	MYLIP	GRCh38.p7	6:16143129	ATAGAATGGCATTCT[A/G]TGCGGGATAGCGAAG	29116
rs759691355	snp	A/G			intron-variant	MYLIP	GRCh38.p7	6:16134204	GAGCTTATCAACATT[A/G]TATCCCCAGAGTCTA	29116
rs759813677	snp	C/T	2.9172e-05	0.00381905	utr-variant-3-prime, intron-variant	MYLIP	GRCh38.p7	6:16146761	ATCTAATCTGTTGTG[C/T]TTTTGTTGGACTTGG	29116
rs759991385	in-del	-/CTGGGGCATAGCAG			intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140700	GAATCGTTCCCTATC[-/CTGGGGCATAGCAG]CTGCAGGGAATGACA	29116
rs760002701	snp	C/T	1.64732e-05	0.0028699	synonymous-codon, intron-variant	MYLIP	GRCh38.p7	6:16130640	AAGTTTATGGCTAAA[C/T]CTGAGAAACCGGATC	29116
rs760053998	snp	A/G	0.000118715	0.00770348	intron-variant	MYLIP	GRCh38.p7	6:16129414	GCCTCAACCAGGTGA[A/G]GGCGAGGGGCAAGAA	29116
rs760153166	snp	C/T	1.65108e-05	0.00287317	missense, downstream-variant-500B, utr-variant-5-prime	MYLIP, MIR4639	GRCh38.p7	6:16141656	CACATCAAGGAGGCC[C/T]TCTTGGCAGGCCACC	29116
rs760153641	snp	A/G	1.66291e-05	0.00288345	intron-variant	MYLIP	GRCh38.p7	6:16143898	GGTCACCTCAGCACC[A/G]CAGCTCTCAGGTTTT	29116
rs760174623	snp	A/T			intron-variant	MYLIP	GRCh38.p7	6:16133214	TGGGCCCAGCTCTAC[A/T]TCCTACTTGAAGGCC	29116
rs760206122	snp	A/G			intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16141513	ATGTTAAGCATTTTC[A/G]GTGTGACTTTTAAAA	29116
rs760380055	snp	A/C	1.64727e-05	0.00286986	missense	MYLIP	GRCh38.p7	6:16145064	GGAGGGCTCTGTACA[A/C]TGCTGGCGTTGTGGA	29116
rs760397067	in-del	-/AA			intron-variant	MYLIP	GRCh38.p7	6:16144130	CATTAATCTAGACAC[-/AA]AGTGTGTTAGGAGAT	29116
rs760685643	snp	C/T	2.13577e-05	0.00326778	synonymous-codon, intron-variant	MYLIP	GRCh38.p7	6:16146721	CTATCTGCCAACGCA[C/T]ACCAGTCTTCTCAAT	29116
rs760771824	snp	C/T	2.22156e-05	0.00333276	missense, intron-variant	MYLIP	GRCh38.p7	6:16146674	CAGTCATGTCCCGTC[C/T]GCAGGTCGCGTGTGG	29116
rs760950801	snp	A/G			intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16139959	TACTTCTTAGTGAAA[A/G]TAAGATTAATGGCTC	29116
rs761024185	snp	G/T	1.64852e-05	0.00287094	missense, intron-variant	MYLIP	GRCh38.p7	6:16130584	CTGGGAATCATAGAA[G/T]TTGACTATTTTGGAC	29116
rs761079482	in-del	-/G			intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140475	TTTATGTACATTTTT[-/G]GAGCTCTCTGATGTT	29116
rs761153319	in-del	-/GA			intron-variant	MYLIP	GRCh38.p7	6:16137686	AGATAATTGCTTTAT[-/GA]GACAAGCCTGTGTTT	29116
rs761210455	snp	C/T	1.64746e-05	0.00287002	stop-gained, intron-variant	MYLIP	GRCh38.p7	6:16130662	AACCGGATCTCCCAG[C/T]AGATGGATGGGCTAG	29116
rs761281680	in-del	-/T	5.05055e-05	0.00502496	intron-variant	MYLIP	GRCh38.p7	6:16130530	CGTACCATTTGCTCA[-/T]CCAGGCTGCATTCCT	29116
rs761323849	snp	A/G	4.94466e-05	0.00497201	missense, intron-variant	MYLIP	GRCh38.p7	6:16143721	TATCCTGTGGTGCAG[A/G]TGGCCACCCAGTCAG	29116
rs761404521	snp	C/G	1.64727e-05	0.00286986	missense	MYLIP	GRCh38.p7	6:16145032	AAGAACATCAAAGGA[C/G]GTGTATGACCATGCC	29116
rs761517644	snp	G/T			intron-variant	MYLIP	GRCh38.p7	6:16137306	TAAACTGTGGTTAAG[G/T]GACTCATTGGACTGA	29116
rs761673305	snp	A/G	1.65154e-05	0.00287358	intron-variant	MYLIP	GRCh38.p7	6:16142977	TTTATCTCTAAAGCT[A/G]ATATCTGTATACTTA	29116
rs761891178	snp	C/T			intron-variant	MYLIP	GRCh38.p7	6:16143506	CACTTGCTCCCATAC[C/T]TCCCTCCACATATGC	29116
rs761900524	snp	A/G	5.4796e-05	0.00523402	missense, utr-variant-5-prime	MYLIP	GRCh38.p7	6:16129399	CCAACGGCGAGGACT[A/G]CCTCAACCAGGTGAG	29116
rs761905930	snp	A/G	1.66081e-05	0.00288163	missense, downstream-variant-500B, utr-variant-5-prime	MYLIP, MIR4639	GRCh38.p7	6:16141777	ACTATGAGGAGCTCT[A/G]TGCCAAGGAGCTCTC	29116
rs761995947	snp	C/T	1.69795e-05	0.00291367	missense	MYLIP	GRCh38.p7	6:16145270	AACTCCACCTTCTGT[C/T]CCTGTGGCCACACTG	29116
rs762090699	snp	A/T			intron-variant	MYLIP	GRCh38.p7	6:16132527	TGTATGGAAAAGTTA[A/T]GTGTGACCTTAACTT	29116
rs762101742	snp	A/G	1.65083e-05	0.00287296	synonymous-codon, intron-variant	MYLIP	GRCh38.p7	6:16143699	CTTCCTGTCTCTTAG[A/G]ATAGCTTATCCTGTG	29116
rs762117805	snp	C/G			intron-variant	MYLIP	GRCh38.p7	6:16138379	CAATCCAGATGGTTT[C/G]AGGGGAAAATACTAA	29116
rs762202962	snp	A/C/G	8.24088e-05	0.0064186	missense	MYLIP	GRCh38.p7	6:16143217	TTAGCCCAATTAATA[A/C/G]GTAAGCCAAGACTTA	29116
rs762404557	in-del	-/GCAAAGGTGAAAGTT	1.64732e-05	0.0028699	cds-indel, intron-variant	MYLIP	GRCh38.p7	6:16130615	TGCAGTTTACGGGTA[-/GCAAAGGTGAAAGTT]TATGGCTAAACCTGA	29116
rs762482981	snp	C/T			intron-variant, upstream-variant-2KB	MYLIP, MIR4639	GRCh38.p7	6:16140035	TTTGTAGCCTCACTG[C/T]CTCCTCCTTAGTCGA	29116
rs762810082	snp	A/T	6.72111e-05	0.00579664	missense	MYLIP	GRCh38.p7	6:16145258	GAGGAGGAGATCAAC[A/T]CCACCTTCTGTCCCT	29116
rs762827020	snp	A/G	3.30967e-05	0.00406783	missense, downstream-variant-500B, utr-variant-5-prime	MYLIP, MIR4639	GRCh38.p7	6:16141755	AACCAGAACACTGCC[A/G]AGTATAACTATGAGG	29116
rs762986029	snp	A/G	1.64732e-05	0.0028699	missense	MYLIP	GRCh38.p7	6:16143133	AATGGCATTCTGTGC[A/G]GGATAGCGAAGGGCA	29116
rs763042096	snp	C/G	1.65274e-05	0.00287462	missense	MYLIP	GRCh38.p7	6:16145181	TCAGCTGCCAGCAGA[C/G]CCGGGTGCTGCAGGA	29116
rs763226361	snp	C/T	3.29571e-05	0.00405924	missense	MYLIP	GRCh38.p7	6:16143207	AAAGATGACTTTAGC[C/T]CAATTAATAGGTAAG	29116
rs763242633	snp	A/T			downstream-variant-500B, intron-variant	MYLIP	GRCh38.p7	6:16148350	TCCTCCTACCGGGAA[A/T]TTAATTTTTTTTTTT	29116

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