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

MED16

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs6678	snp	A/G	0.355609	0.226598	synonymous-codon, utr-variant-5-prime	MED16	GRCh38.p7	19:890165	CTCCAGGCAGGTGAT[A/G]GCCTCGTGGTGCTCT	10025
rs11492	snp	A/C	0.0112582	0.074178	synonymous-codon	MED16	GRCh38.p7	19:886088	CAGGGACACGGTGAC[A/C]AGGCCGCTGACCGTC	10025
rs13090	snp	A/G	0.382621	0.211936	missense	MED16	GRCh38.p7	19:868115	GACCATCTGCATCCA[A/G]AGGACCGTCCGTGAC	10025
rs891206	snp	C/T	0.493201	0.0579089	intron-variant	MED16	GRCh38.p7	19:872255	TCGGTGCCAGAAGCA[C/T]CCCAGTCCTGACCAC	10025
rs1060442	snp	C/T	0.4794	0.0993767	synonymous-codon	MED16	GRCh38.p7	19:885818	CCGCAAGGACAAGTT[C/T]CCCGCCATCACCCAC	10025
rs1616408	snp	C/T	0.498568	0.0267188	intron-variant	MED16	GRCh38.p7	19:877516	GGTCAGTGGGGTGGC[C/T]CACAGCACGTATTAG	10025
rs1617214	snp	C/G	0.338069	0.233974	intron-variant	MED16	GRCh38.p7	19:877437	ACTCCTCAGGTAAAG[C/G]AGACGAGTGTAAGCC	10025
rs1631848	snp	A/G	0.39544	0.20334	intron-variant	MED16	GRCh38.p7	19:868551	AAGTGGGGCAGGCGT[A/G]AGGGAGGCCCGCCTG	10025
rs1651881	snp	A/G	0	0	intron-variant	MED16	GRCh38.p7	19:878805	GAGCTGCTGGGGCAC[A/G]TGGGGCTGGGGCTGG	10025
rs1651882	snp	A/G	0.321292	0.23962	intron-variant	MED16	GRCh38.p7	19:878721	TGGTGGGGATTGACA[A/G]CCAGGGGAAGGCGAG	10025
rs1651883	snp	C/T			intron-variant	MED16	GRCh38.p7	19:879287	ACAACCATGGGAAGG[C/T]GAGCTGCTGGGCATT	10025
rs1651884	snp	C/T			intron-variant	MED16	GRCh38.p7	19:879199	ACAACCATGGGAAGG[C/T]GAGCTGCTGGGCATT	10025
rs1651885	snp	G/T			intron-variant	MED16	GRCh38.p7	19:879123	TGGGGCTGGGGCTGG[G/T]GGGTATTGACAACCA	10025
rs1651886	snp	A/G	0.350764	0.228794	intron-variant	MED16	GRCh38.p7	19:876641	CAGGTAGCCTGTGGC[A/G]GGTGAGGCTGCGTGT	10025
rs1651887	snp	C/T	0.298651	0.24522	intron-variant	MED16	GRCh38.p7	19:875902	CTCTCCAACTCCCAG[C/T]CTCCAGGAATCCTCC	10025
rs1651888	snp	C/T	0.368529	0.220116	intron-variant	MED16	GRCh38.p7	19:873743	CTCCCAGTTCCTCTC[C/T]GTCCGGCAACGCCAT	10025
rs1651889	snp	C/G	0.488118	0.0761554	intron-variant	MED16	GRCh38.p7	19:873341	TCAGCCCCGCCCCTA[C/G]TTGGAGTCCCGCCCC	10025
rs1651890	snp	C/G	0.393987	0.204372	intron-variant	MED16	GRCh38.p7	19:870946	CACGGCTCCCTCCCT[C/G]CATGTCCTGCCCCAG	10025
rs1651891	snp	C/T	0.279991	0.248195	intron-variant	MED16	GRCh38.p7	19:868620	TGTGGCAGGTGGGGA[C/T]GTGGGGAGCAGGCGT	10025
rs1683565	snp	C/T	0.368119	0.220336	intron-variant	MED16	GRCh38.p7	19:880602	GGACTCCTTTCATAT[C/T]CTCTTTTCCATGAGC	10025
rs1683566	snp	C/T	0.367091	0.220884	intron-variant	MED16	GRCh38.p7	19:880560	GACCCCACCTCCCCC[C/T]GGCCCTCGTACAATG	10025
rs1683567	snp	G/T			intron-variant	MED16	GRCh38.p7	19:879175	GGGCATTGACAACCA[G/T]GGGAAGGCGAGCTgc	10025
rs1683568	snp	A/C	0.0209421	0.100162	intron-variant	MED16	GRCh38.p7	19:879047	gTGGGCATTGACAAC[A/C]GGGGGAAGGTGAGCT	10025
rs1683569	snp	A/G	0.402052	0.198444	synonymous-codon	MED16	GRCh38.p7	19:871135	GGGCTGCAGGCGGCT[A/G]ACCAGGCCGTCGCTG	10025
rs1683570	snp	A/G	0.434543	0.168653	intron-variant	MED16	GRCh38.p7	19:871447	GCTGGGTGACCCCAG[A/G]GTTCTCTCCCCGTCT	10025
rs1683573	snp	A/G	0.500538	0.0133903	intron-variant	MED16	GRCh38.p7	19:872614	CCGGGTGGGTGGGGC[A/G]GAAGAAATCACAGCT	10025
rs1683574	snp	A/G	0.458272	0.138286	intron-variant	MED16	GRCh38.p7	19:872877	CGGGGCTTTGAGAAT[A/G]GGCAGGAAGGGTGTG	10025
rs1683575	snp	C/G	0.434976	0.168179	intron-variant	MED16	GRCh38.p7	19:873258	GGGGTGGGACTCCAA[C/G]CAGGGGCGGGGCTGA	10025
rs1683576	snp	C/G	0.0573587	0.15934	intron-variant	MED16	GRCh38.p7	19:873962	CTGCAGCCACCCCCG[C/G]CTGGCAGCTGGCGGC	10025
rs1683588	snp	C/T	0.262985	0.249663	intron-variant	MED16	GRCh38.p7	19:870489	actgcaacgtctgcc[C/T]ctcgggttcaaatga	10025
rs1683589	snp	A/G	0	0	intron-variant	MED16	GRCh38.p7	19:869564	GGGGCCTCCTAATGA[A/G]TCACACACGAGGGTT	10025
rs1683590	snp	C/T	0.388775	0.207946	intron-variant	MED16	GRCh38.p7	19:869496	GTTACGTCAGAGGCT[C/T]GTAAACTGGGAAAAT	10025
rs1683591	snp	C/T	0.38934	0.207568	intron-variant	MED16	GRCh38.p7	19:869037	TGTGAGGCCGGCCAT[C/T]CCCTCCACCCCCGCC	10025
rs1683592	snp	C/T	0.258843	0.249844	downstream-variant-500B	MED16	GRCh38.p7	19:867774	GTGGATGGGATGGGG[C/T]GGCCATCGTCAGGGT	10025
rs1683593	snp	C/T	0.369142	0.219784	downstream-variant-500B	MED16	GRCh38.p7	19:867735	TCCAGGCATCTGCCT[C/T]TCAGTGTGTTGTCTG	10025
rs2241623	snp	A/G	0.424193	0.179323	intron-variant	MED16	GRCh38.p7	19:876604	TGCTCCCAGAGGCCC[A/G]TCCAGGAAAGCTGCA	10025
rs2288546	snp	A/G	0.144969	0.226867	intron-variant	MED16	GRCh38.p7	19:871457	GACAGGCCAGAGACG[A/G]GGAGAGAACTCTGGG	10025
rs2303820	snp	A/G	0.0146672	0.084371	intron-variant	MED16	GRCh38.p7	19:869061	CATCTGGGCCCACCT[A/G]GCAGATGGTGTGAGG	10025
rs2365702	snp	A/G	0.406296	0.19512	intron-variant	MED16	GRCh38.p7	19:881413	CCCATCAGAACCCAG[A/G]AGGCTGAGCTCCTAC	10025
rs2365703	snp	A/G	0.439502	0.163061	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:892615	CTCCAGACCCCTATA[A/G]CTCCGCAGTCCCCAG	10025
rs2365704	snp	A/C	0.5	0	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:892888	GAGCCCCGAGCCCCG[A/C]GCCCCGCGCCCCGCG	10025
rs2365705	snp	A/C	0.5	0	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:892895	gagccccgagccccg[A/C]gccccgcgccccgcg	10025
rs2629995	snp	C/G	0.5	0	intron-variant	MED16	GRCh38.p7	19:879480	GTGGGGCTGGGGCTG[C/G]TGGGCATTGACAACC	10025
rs2629996	snp	A/G	0.346368	0.23068	intron-variant	MED16	GRCh38.p7	19:878598	GGCGTTGACAACCAC[A/G]GGAAGGTGAGCTGCT	10025
rs2930891	snp	C/T	0.370974	0.218781	intron-variant	MED16	GRCh38.p7	19:883224	ATGCCAGGCTTCGGT[C/T]CCTACCATGCCCAGC	10025
rs2930892	snp	C/T	0.482831	0.0910472	intron-variant	MED16	GRCh38.p7	19:882943	CCACTGTGTGCCCTC[C/T]GGGCGTCTCAGCCAC	10025
rs2930893	snp	C/G	0.319616	0.240112	intron-variant	MED16	GRCh38.p7	19:882724	GCCAGCAGCCCTGCA[C/G]TGTTTCTGTTTCTGT	10025
rs2930894	snp	C/T	0.367091	0.220884	intron-variant	MED16	GRCh38.p7	19:881161	CACACTCTTCAGTGC[C/T]TACCCTATTTGCTCA	10025
rs2930895	snp	C/T	0.450985	0.148678	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:893080	GGCCGACCAGGTGAG[C/T]GCGGGGCTGCGGGGG	10025
rs2930896	snp	C/G	0.48	0.0979796	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:891740	AGGTGTTCCCTGTCA[C/G]TCAGCCCCGCCTCGG	10025
rs2930898	snp	C/T	0.374	0.217081	intron-variant	MED16	GRCh38.p7	19:883968	GGGAAGGAATGGCAG[C/T]GGCCCTCTTCACCTT	10025
rs2930899	snp	C/G	0.402806	0.197864	intron-variant	MED16	GRCh38.p7	19:885398	GGGCCGCCTCTCACA[C/G]AGAAGGGACCTGCGG	10025
rs2930900	snp	A/G	0.255224	0.249945	intron-variant	MED16	GRCh38.p7	19:886257	CATGGGGGCTGCCCC[A/G]TGACCCCCAGAAACA	10025
rs2930901	snp	A/G	0.344815	0.231323	intron-variant	MED16	GRCh38.p7	19:886945	ttagccgggcatggt[A/G]gcgggtgcctataat	10025
rs2930902	snp	A/G	0.141687	0.225598	intron-variant	MED16	GRCh38.p7	19:887128	TCTACGTTGTGAAAA[A/G]ATGCGAGGAAGAGAA	10025
rs2930903	snp	C/G	0.499776	0.0105807	intron-variant	MED16	GRCh38.p7	19:887824	ggacaggcagatcca[C/G]agagacaactgggtc	10025
rs2930904	snp	A/G	0.0271762	0.113356	intron-variant	MED16	GRCh38.p7	19:888161	gtgagccgagatcgc[A/G]ccactacactccagc	10025
rs2930905	snp	C/T	0.270351	0.24917	intron-variant	MED16	GRCh38.p7	19:888663	GGTCTGTGAACTCCA[C/T]CCCGACAAAACTGTT	10025
rs2965290	snp	A/G	0.401747	0.198678	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:892003	CAGGTGTTCCCCGTC[A/G]CACTCAGCCCCGCCT	10025
rs2965291	snp	C/G/T	0.266273	0.24947	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:891948	CTCAGCCCCCGGCTC[C/G/T]GCCACAGGTGTTCCC	10025
rs2965292	snp	C/T	0.348354	0.22984	intron-variant	MED16	GRCh38.p7	19:890844	ACCTCTCACTCACCC[C/T]GGCCCTCCTCTGTAA	10025
rs2965293	snp	A/G	0.344147	0.231595	intron-variant	MED16	GRCh38.p7	19:888384	GGCACCCACCACCAC[A/G]CCTGGCTAATTTTTG	10025
rs2965294	snp	C/G	0.493748	0.0555599	intron-variant	MED16	GRCh38.p7	19:884782	CGGCCCTAAGCGATC[C/G]TCTCGCCTCGATCTC	10025
rs3111332	snp	C/T			intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:892886	ctgagccccgagccc[C/T]gagccccgagccccg	10025
rs3217342	in-del	-/TCCTCAGCTAC	0.000404904	0.0142228	intron-variant	MED16	GRCh38.p7	19:868340	CTACTCCTCAGCTAC[-/TCCTCAGCTAC]CCCTCAGCTGCCCCT	10025
rs4417648	snp	A/G	0.37138	0.218556	intron-variant	MED16	GRCh38.p7	19:883725	GACACAGACGTGCCC[A/G]GCGGGGGCACCGGGC	10025
rs4806813	snp	A/G	0.40086	0.199352	intron-variant	MED16	GRCh38.p7	19:881094	CAGGGAAGAACGGGA[A/G]CTGGGGGAAGAAAGG	10025
rs4807142	snp	C/T	0.404384	0.196635	intron-variant	MED16	GRCh38.p7	19:874960	TTGAGGTCAAGAGTT[C/T]GAGACCAGCCTGGCC	10025
rs4807153	snp	A/G	0.404035	0.196909	intron-variant	MED16	GRCh38.p7	19:881049	CCCTGAGCCCCGAGC[A/G]GGTTTTGATAAATGC	10025
rs7253106	snp	G/T	0.0314385	0.121371	intron-variant	MED16	GRCh38.p7	19:885468	TGGGGGGGGTCCGGG[G/T]GCCCCAGTGTCCTCA	10025
rs7253460	snp	C/G	0.402982	0.197728	intron-variant	MED16	GRCh38.p7	19:885706	GGTCTCCACCCCCAG[C/G]ACCCTGAGAAGCAGT	10025
rs7256798	snp	A/G	0.0283406	0.115616	intron-variant	MED16	GRCh38.p7	19:870213	GGGGCCAGAGACTAA[A/G]GGCAGAGGCTAAGGC	10025
rs7257260	snp	A/G	0.0142736	0.0832652	intron-variant	MED16	GRCh38.p7	19:870592	aaaaaaaGGGAGAGG[A/G]TGAATGGAAGGGCTG	10025
rs8100009	snp	A/G	0.0176367	0.0922351	synonymous-codon	MED16	GRCh38.p7	19:871048	GCACCTGGCGAGGCC[A/G]TCGAGCTGCAGGGTG	10025
rs8100258	snp	A/G	0.370503	0.219041	synonymous-codon	MED16	GRCh38.p7	19:871222	ATCCACCAGCGCCTC[A/G]TCCGGCTCGCTCGCT	10025
rs8105744	snp	A/G	0.343477	0.231866	downstream-variant-500B	MED16	GRCh38.p7	19:867595	TGGAGAAACATAACA[A/G]GGACAGAGTCAGGCA	10025
rs9676834	snp	A/G			intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:891613	ACAGGGAACACCTGT[A/G]GCCGAGGCGGGGCTG	10025
rs10401425	snp	C/G			intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:892682	CGCACCGATAACCCC[C/G]CAGTCTCCAGGCCCT	10025
rs10412830	snp	C/T			intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:892688	GATAACCCCGCAGTC[C/T]CCAGGCCCTGCCTCT	10025
rs10414386	snp	A/G			intron-variant	MED16	GRCh38.p7	19:876911	GGCCCCACCTGCCAC[A/G]GGGCCCCCACCTGCC	10025
rs10415140	snp	C/G	0.467234	0.12373	upstream-variant-2KB	MED16	GRCh38.p7	19:894169	gcctcccgagtagct[C/G]ggactacaggcgcgc	10025
rs10415271	snp	A/C/T	0.5	0	intron-variant	MED16	GRCh38.p7	19:870222	GACTAAGGGCAGAGG[A/C/T]TAAGGCAGGGCGCCC	10025
rs10415544	snp	C/T			intron-variant	MED16	GRCh38.p7	19:870392	attgcaaaaccgcct[C/T]tataccaaaaataca	10025
rs10422235	snp	C/G	0.479824	0.098392	upstream-variant-2KB	MED16	GRCh38.p7	19:895062	ctgcactccagcctg[C/G]gggacagagcaagac	10025
rs10424998	snp	C/G	0.243061	0.249904	intron-variant	MED16	GRCh38.p7	19:874647	CAGGAGTAGAGAgag[C/G]tgaaaggatcgcttg	10025
rs10425005	snp	A/G	0.276534	0.248588	intron-variant	MED16	GRCh38.p7	19:874658	Agaggtgaaaggatc[A/G]cttgagctcaggtgg	10025
rs10425219	snp	C/G	0.0209421	0.100162	intron-variant	MED16	GRCh38.p7	19:874779	tccagaggctgaggc[C/G]agattgcttgagccc	10025
rs10451478	snp	C/G	0.0644693	0.167566	intron-variant	MED16	GRCh38.p7	19:883883	TGGGGACCGGGCGAA[C/G]GAACGAGCCCTGGGA	10025
rs11085228	snp	A/G	0.0741063	0.177655	intron-variant	MED16	GRCh38.p7	19:883464	GGCATGGCGGGGACC[A/G]AAGCCTGGCATGGTG	10025
rs11546307	snp	C/T	0.329837	0.236909	synonymous-codon	MED16	GRCh38.p7	19:875389	GCCCTGCACGGTGAC[C/T]CGCGTGTGCGACTAC	10025
rs11878213	snp	C/T	0.497271	0.0368399	upstream-variant-2KB	MED16	GRCh38.p7	19:894722	aggacagcttgagtt[C/T]gagaccagcctggga	10025
rs11878467	snp	C/T	0.0429648	0.14013	intron-variant	MED16	GRCh38.p7	19:889982	CACCCTGAACAAGAA[C/T]GATTCGGGCCACTAT	10025
rs11878621	snp	C/T	0.0429648	0.14013	intron-variant	MED16	GRCh38.p7	19:890073	GACTGACCGGAGAAA[C/T]ACAGGGCCCCCCTGC	10025
rs11879638	snp	C/G	0.479904	0.0982045	upstream-variant-2KB	MED16	GRCh38.p7	19:894790	aaattagcagggttg[C/G]ggagggaggggcgct	10025
rs11879857	snp	A/G	0.0494327	0.149241	intron-variant	MED16	GRCh38.p7	19:882481	gtgagccaagatcac[A/G]ccactgcactccagc	10025
rs11879886	snp	A/G	0.0144652	0.0838055	intron-variant	MED16	GRCh38.p7	19:889821	GCCTGAGGGCAAGAA[A/G]CCATCATTGCGAACC	10025
rs11879913	snp	A/G	0.0429648	0.14013	intron-variant	MED16	GRCh38.p7	19:889918	AGAGGTCTCGGCCCA[A/G]GTAGGGCACAGCAGG	10025
rs11883077	snp	A/G	0.0429648	0.14013	intron-variant	MED16	GRCh38.p7	19:889898	GGGGGAAGCCAGCCC[A/G]GTGGAGAGGTCTCGG	10025
rs12460696	snp	A/G	0.393065	0.205018	intron-variant	MED16	GRCh38.p7	19:870453	GTAATCCCAGCTACT[A/G]GGAAGGCTGAGGTAG	10025
rs12461907	snp	G/T			intron-variant	MED16	GRCh38.p7	19:872586	GAAGGGCGGGCCCCA[G/T]GGCAGGATGAAGCCG	10025
rs12462332	snp	A/C	0.5	0	intron-variant	MED16	GRCh38.p7	19:870143	gccctgggccaTATG[A/C]TAAGGCGTCTCTCTC	10025
rs12462823	snp	C/G	0.0644968	0.167596	synonymous-codon	MED16	GRCh38.p7	19:886001	GGTGAAGGCGATGTC[C/G]GCCAGGGCCACGCGG	10025
rs12973405	snp	C/G			intron-variant	MED16	GRCh38.p7	19:877879	GCAGCTCGCCTTCCC[C/G]TGGTTGTCAATGCCC	10025
rs12973585	snp	C/G			intron-variant	MED16	GRCh38.p7	19:877900	GTCAATGCCCACCAG[C/G]CCCAGCCCCACGTGC	10025
rs12979753	snp	A/G	0.444444	0.157135	intron-variant	MED16	GRCh38.p7	19:877815	GTGCCCCAGCAGCTC[A/G]CCTTCCCGTGGTTGT	10025
rs12979761	snp	C/G			intron-variant	MED16	GRCh38.p7	19:877823	gcAGCTCGCCTTCCC[C/G]TGGTTGTCAATGCCC	10025
rs12979807	snp	A/G			intron-variant	MED16	GRCh38.p7	19:877899	TGTCAATGCCCACCA[A/G]CCCCAGCCCCACGTG	10025
rs12979858	snp	C/T			intron-variant	MED16	GRCh38.p7	19:878014	TTCCGTGGTTGTCAA[C/T]GCCCAccagccccag	10025
rs12980020	snp	A/G			intron-variant	MED16	GRCh38.p7	19:877912	CAGCCCCAGCCCCAC[A/G]TGCCCCAGCAGCTCA	10025
rs12980038	snp	C/G	0.00874735	0.0655527	intron-variant	MED16	GRCh38.p7	19:877935	GCAGCTCACCTTCCC[C/G]TGGTTGTCAATGCCC	10025
rs12980050	snp	G/T			intron-variant	MED16	GRCh38.p7	19:877947	CCCGTGGTTGTCAAT[G/T]CCCAccagccccagc	10025
rs12982619	snp	A/G			intron-variant	MED16	GRCh38.p7	19:872963	ggggagggctccgag[A/G]tggggcagggctccg	10025
rs12984209	snp	C/T			intron-variant	MED16	GRCh38.p7	19:878000	ccagcAGCTCACCTT[C/T]CCGTGGTTGTCAACG	10025
rs12985432	snp	A/G			intron-variant	MED16	GRCh38.p7	19:877856	CAAGCCCAGCCCCAC[A/G]TGCCCCAGCAGCTCG	10025
rs12985652	snp	A/G			intron-variant	MED16	GRCh38.p7	19:877927	GTGCCCCAGCAGCTC[A/G]CCTTCCCGTGGTTGT	10025
rs13339757	snp	A/G	0.00478085	0.0486577	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:891805	ACCTGTGGCCGAGGC[A/G]GGGCTGAGTGTGACG	10025
rs28375818	snp	C/G	0.402277	0.198272	intron-variant	MED16	GRCh38.p7	19:879649	GCCCCAGCAGCTCAC[C/G]TTCCCCTGGTTGTCA	10025
rs28384237	snp	A/G			intron-variant	MED16	GRCh38.p7	19:879879	AATGCCCAGCAGCTC[A/G]CCTTCCCCTGGTTGT	10025
rs28414042	snp	C/T			intron-variant	MED16	GRCh38.p7	19:879659	CTCACGTTCCCCTGG[C/T]TGTCAATGCCCACCA	10025
rs28458775	snp	A/C/G			intron-variant	MED16	GRCh38.p7	19:879784	GCCCCACGTGCCCCA[A/C/G]CAGCTCGCCTTCCCC	10025
rs28463488	snp	A/G			intron-variant	MED16	GRCh38.p7	19:879703	GTGCCCCAGCAGCTC[A/G]CCTTCCCCTGGTTGT	10025
rs28468554	snp	A/C	0.404907	0.196224	upstream-variant-2KB, downstream-variant-500B	MED16, RNU6-9	GRCh38.p7	19:893793	GTAGAGACGGGGTTT[A/C]GCCATGTTGGCCAGG	10025
rs28499161	snp	A/C/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:879840	GCCCCACGTGCCCCA[A/C/G]CAGCTCACCTTCCCC	10025
rs28545193	snp	C/G	0.00155074	0.0278023	intron-variant	MED16	GRCh38.p7	19:879887	GCAGCTCGCCTTCCC[C/G]TGGTTGTCAATGCCC	10025
rs28578406	snp	A/G	0.00276353	0.0370692	synonymous-codon	MED16	GRCh38.p7	19:875337	GCAGCAGCGACTTCA[A/G]GGTGGAGCTGATGGC	10025
rs28604587	snp	C/G			intron-variant	MED16	GRCh38.p7	19:879655	GCAGCTCACGTTCCC[C/G]TGGTTGTCAATGCCC	10025
rs28626160	snp	A/G	0.498673	0.0257246	upstream-variant-2KB, downstream-variant-500B	MED16, RNU6-9	GRCh38.p7	19:893910	TTTCTTCCATTTTCT[A/G]ATGTCCAAGAGTGGG	10025
rs34023764	in-del	-/T			intron-variant	MED16	GRCh38.p7	19:887899	GACTGGGTTTCCTTT[-/T]CGGGTGATGAGAAGG	10025
rs34110403	snp	A/C/G/T	0.00141472	0.0265668	missense	MED16	GRCh38.p7	19:871146	GGCTAACCAGGCCGT[A/C/G/T]GCTGGCTGGCAGCCA	10025
rs34545691	snp	C/T	0.00023687	0.0108802	synonymous-codon, utr-variant-5-prime	MED16	GRCh38.p7	19:886196	TTCTCCACAGTCGGG[C/T]GCCTCCAGCTTCGGG	10025
rs34583289	in-del	-/A			intron-variant	MED16	GRCh38.p7	19:888543	AAAAAAAAAAAAAAA[-/A]GATAAAGGTCTGAGG	10025
rs34669461	snp	A/C	0.00112921	0.0237345	synonymous-codon	MED16	GRCh38.p7	19:880141	CCCCACAGGGCTGGC[A/C]CTGGCCTTCCACGAC	10025
rs34713707	in-del	-/C			intron-variant	MED16	GRCh38.p7	19:875782	CAACAGGACACCCCC[-/C]ATCCCAGAGGCTGCT	10025
rs34792568	in-del	-/A			intron-variant	MED16	GRCh38.p7	19:880579	GAGGTGGGGTCCAGA[-/A]GCCCAAAGCTCATGG	10025
rs34799086	snp	C/T	0.34209	0.232421	synonymous-codon	MED16	GRCh38.p7	19:880066	CGTCTTCTACAGCTC[C/T]GCGGCCCCGAGGCCT	10025
rs34828577	snp	A/G	0.480064	0.0978296	downstream-variant-500B	MED16	GRCh38.p7	19:867872	CCATAAATGCTGAAG[A/G]ATTTAAAGACAGGCC	10025
rs34859566	snp	C/T	0.000992415	0.0222536	missense	MED16	GRCh38.p7	19:871044	CTGCAGCTCGACGGC[C/T]TCGCCAGGTGCGTGT	10025
rs35040519	snp	C/T	0.0131391	0.0799806	synonymous-codon	MED16	GRCh38.p7	19:868421	GCGCTGGATCAAGAA[C/T]TGCCTGTGCGGTGGG	10025
rs35178920	in-del	-/T			intron-variant	MED16	GRCh38.p7	19:868568	GCCTGCCCCACTTTT[-/T]GCTTCCAGGCAGGTC	10025
rs35223165	in-del	-/AC	0.0460142	0.144533	intron-variant	MED16	GRCh38.p7	19:886272	ATGACCCCCAGAAAC[-/AC]GCGCACAGAAGAACC	10025
rs35226201	in-del	-/C			intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:892079	CGGGGGCTGAGTGTC[-/C]ACAGGGAACAGAGGG	10025
rs35267984	snp	C/T	0.00318978	0.0398085	intron-variant	MED16	GRCh38.p7	19:886743	GTCATTATTGACATA[C/T]GGAAACATCCACCCT	10025
rs35361724	snp	C/T	0.000781861	0.0197565	synonymous-codon	MED16	GRCh38.p7	19:871189	ATGCTGCCTGCTGCC[C/T]AGCCAGCTGCTTATC	10025
rs35425458	in-del	-/T			intron-variant	MED16	GRCh38.p7	19:882902	CCTGTGAGCAGCATT[-/T]CCCTGGGGGGAAACA	10025
rs35446283	in-del	-/C/TGG	0.0287284	0.116357	intron-variant	MED16	GRCh38.p7	19:887246	GAAGCAAGCCAGGCC[-/C/TGG]TGGTGGTGAGGGGTT	10025
rs35491416	in-del	-/C			intron-variant	MED16	GRCh38.p7	19:883949	GACTCACTACAAGCC[-/C]TGGGGGAAGGAATGG	10025
rs35542830	snp	C/T	0.00679489	0.0578902	synonymous-codon	MED16	GRCh38.p7	19:886082	CAGCGGCCTGGTCAC[C/T]GTGTCCCTGCTGAAG	10025
rs35695678	snp	A/C	0.00240233	0.0345745	synonymous-codon	MED16	GRCh38.p7	19:880078	GCAGACCATGGCCGT[A/C]TTCTACAGCTCCGCG	10025
rs35799269	in-del	-/G			frameshift-variant	MED16	GRCh38.p7	19:871141	AGGCGGCTAACCAGG[-/G]CCGTCGCTGGCTGGC	10025
rs35944606	in-del	-/T			intron-variant	MED16	GRCh38.p7	19:884440	GGTGGGGGGCGTGTT[-/T]CTCAGCAGCCTCAGC	10025
rs55639032	snp	C/T	0.221737	0.248397	intron-variant	MED16	GRCh38.p7	19:869198	CTTGAGGCTTAGAGA[C/T]CCAGTAAAGGGGACG	10025
rs55668554	snp	A/G			intron-variant	MED16	GRCh38.p7	19:878091	TGCCCCCCAGCCCCA[A/G]CCCCAGCGCCACGTG	10025
rs55735124	snp	A/G			intron-variant	MED16	GRCh38.p7	19:878438	ACCAGCCCCAGCCCC[A/G]GCCCCGGCCCCGGCC	10025
rs55896161	snp	C/T	0.00755907	0.0610114	intron-variant	MED16	GRCh38.p7	19:878485	CTCACCTTCCCCTGG[C/T]TGTCAATGCCCACCA	10025
rs55939330	snp	C/T	0.10237	0.201756	intron-variant	MED16	GRCh38.p7	19:877415	GACTGCACTGGATGC[C/T]GAGCCAGGCTTACAC	10025
rs56012113	snp	C/G			intron-variant	MED16	GRCh38.p7	19:878407	GCAGCTCACCTTTCC[C/G]TGGTTGTCAATGTCC	10025
rs56019058	in-del	-/TTT			upstream-variant-2KB, downstream-variant-500B	MED16, RNU6-9	GRCh38.p7	19:893598	ATATTTTTTTTTTTT[-/TTT]CCATTTTCCCTCCCA	10025
rs56090981	snp	C/T			intron-variant	MED16	GRCh38.p7	19:878420	CCCTGGTTGTCAATG[C/T]CCACCAGCCCCAGCC	10025
rs56142163	snp	C/G/T	0.00716266	0.059414	intron-variant	MED16	GRCh38.p7	19:878478	CCAGCAGCTCACCTT[C/G/T]CCCTGGCTGTCAATG	10025
rs56212076	snp	C/T	0.00438332	0.0466095	intron-variant	MED16	GRCh38.p7	19:878404	CCAGCAGCTCACCTT[C/T]CCCTGGTTGTCAATG	10025
rs56228159	snp	A/G	0	0	intron-variant	MED16	GRCh38.p7	19:872802	GGGCAGCAGCAGCAG[A/G]AGCAAGGCGAACCGG	10025
rs56234931	snp	C/T	0.129954	0.219292	intron-variant	MED16	GRCh38.p7	19:890437	GCCTGTGAGGCGCCA[C/T]AACTGTGTCTTTAAA	10025
rs56254546	snp	A/G			intron-variant	MED16	GRCh38.p7	19:878444	CCCAGCCCCGGCCCC[A/G]GCCCCGGCCCCACGT	10025
rs56283881	snp	C/T	0.191147	0.242974	utr-variant-5-prime, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:893183	TCGGTAACAACCAGT[C/T]GCCTGAGGCGTGGGG	10025
rs56291066	snp	C/T			intron-variant	MED16	GRCh38.p7	19:878494	CCCTGGCTGTCAATG[C/T]CCACCAGCCCCAGCC	10025
rs56709858	snp	C/T	0.0429648	0.14013	intron-variant	MED16	GRCh38.p7	19:888020	CCACCCTGACCAACA[C/T]GGAGAAACCCGGTCC	10025
rs56920346	in-del	-/ACTCCAACTAGGGGCGGG					GRCh38.p7	19:873334	CCAAGTAGGGGCGGG[-/ACTCCAACTAGGGGCGGG]GCTGAGGTGGTTTTG	10025
rs57007921	in-del	-/TCAT			intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:891509	TGATGATGGGGGCAG[-/TCAT]CAAGTGGACACTAGC	10025
rs57128987	snp	A/T	0.0554779	0.157039	intron-variant	MED16	GRCh38.p7	19:883427	GGCACGGTGGGCACG[A/T]GGGGCGGTGCGTGAA	10025
rs57536605	snp	A/G	0.0267878	0.112589	intron-variant	MED16	GRCh38.p7	19:870425	AAATACCTAGGTGTG[A/G]TGGCTCATGCCTGTA	10025
rs57793666	in-del	-/TCCCACCA			intron-variant	MED16	GRCh38.p7	19:877890	CCCCTGGTTGTCAAT[-/TCCCACCA]GCCCACCAGCCCCAG	10025
rs58053516	in-del	-/GCCCCA			intron-variant	MED16	GRCh38.p7	19:878040	CCAGCCCCAGCCCCA[-/GCCCCA]CGTGCCCCAGCAGCT	10025
rs58516228	snp	A/G			intron-variant	MED16	GRCh38.p7	19:878855	TGCCCACCAGCCCCA[A/G]CCCCAGCCCCAGCCC	10025
rs58619968	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:874392	GCTGGGATTACACAC[A/G]AGTCGCCACGCCCAG	10025
rs58690545	snp	A/G			intron-variant	MED16	GRCh38.p7	19:878057	GTGCCCCAGCAGCTC[A/G]CCTTCCCCTGGCTGT	10025
rs59181776	snp	A/G	0.158632	0.232706	upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:893271	GGCTATTTGCATACG[A/G]CCATTTCCAGTAATT	10025
rs59303053	snp	A/G/T	0.0429648	0.14013	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:891509	GTGATGATGGGGGCA[A/G/T]CAAGTGGACACTAGC	10025
rs60478125	snp	A/G	0.00517822	0.0506191	intron-variant	MED16	GRCh38.p7	19:870928	GTGTGGATTCGGGGG[A/G]ACCTGGGGCAGGACA	10025
rs60490563	snp	A/G	0.409041	0.192888	intron-variant	MED16	GRCh38.p7	19:882939	GAGAGTGGCTGAGAC[A/G]CCCAGAGGGCACACA	10025
rs60524262	snp	A/G	0.0429648	0.14013	intron-variant	MED16	GRCh38.p7	19:887929	GGACTGAAGCTGGGC[A/G]CAGTGACTCACGCCT	10025
rs60839977	in-del	-/C			intron-variant	MED16	GRCh38.p7	19:877894	TGGTTGTCAATGCCC[-/C]ACCAGCCCCAGCCCC	10025
rs61078208	in-del	-/GCC			intron-variant	MED16	GRCh38.p7	19:877895	GGTTGTCAATGCCCA[-/GCC]CCAGCCCCAGCCCCA	10025
rs61141807	snp	A/G			upstream-variant-2KB	MED16	GRCh38.p7	19:894712	CCAAGGTCTGAGGAC[A/G]GCTTGAGTTTGAGAC	10025
rs61738004	snp	A/G	0.0121981	0.0771378	synonymous-codon	MED16	GRCh38.p7	19:875245	GGAAAAGGACCCACC[A/G]ACGTCGGTGATCTTG	10025
rs61738006	snp	A/G	0.02978	0.118335	synonymous-codon	MED16	GRCh38.p7	19:868236	GCAGGCGTCCGGCCC[A/G]CGGCCTTCAACAGCC	10025
rs61755331	snp	C/T	0.0143302	0.0834252	synonymous-codon	MED16	GRCh38.p7	19:875395	GCACACGCGGGTCAC[C/T]GTGCAGGGCGACAGC	10025
rs62132304	snp	A/G	0.00317557	0.0397203	synonymous-codon, intron-variant	MED16	GRCh38.p7	19:877082	CCACCAGTCGTAGCC[A/G]GTCACCATGCAGTAC	10025
rs62132306	snp	A/G			intron-variant	MED16	GRCh38.p7	19:877871	ATGCCCCAGCAGCTC[A/G]CCTTCCCCTGGTTGT	10025
rs62132307	snp	A/G			intron-variant	MED16	GRCh38.p7	19:877920	GCCCCACGTGCCCCA[A/G]CAGCTCACCTTCCCG	10025
rs62132308	snp	C/G			intron-variant	MED16	GRCh38.p7	19:879743	GCAGCTCGCCTTCCC[C/G]TGGTTGTCAATGCCC	10025
rs62132309	snp	A/G	0.444444	0.157135	intron-variant	MED16	GRCh38.p7	19:879791	GTGCCCCAGCAGCTC[A/G]CCTTCCCCTGGCTGT	10025
rs62132310	snp	G/T	0.5	0	intron-variant	MED16	GRCh38.p7	19:880871	CGGAGGTTGCAGTGA[G/T]CCGAGATCACACCAC	10025
rs62132311	snp	A/G	0.00159617	0.0282053	intron-variant	MED16	GRCh38.p7	19:882621	TGGAGCCGGCCTGCT[A/G]GAGCATGTGCGGCCA	10025
rs62132312	snp	A/G	0.0023933	0.0345097	intron-variant	MED16	GRCh38.p7	19:883018	GACAGGAAACTCAAC[A/G]CCCCAGCGCCGGGGG	10025
rs62132322	snp	G/T	0.187053	0.241946	intron-variant	MED16	GRCh38.p7	19:887226	GAAGCAGGTCCAGAA[G/T]TCCAGGAAGCAAGCC	10025
rs62132323	snp	A/G	0.184203	0.241186	intron-variant	MED16	GRCh38.p7	19:887434	GCACTTTGGGAGGCC[A/G]AGGCGGGCAGATCTC	10025
rs62132324	snp	C/T			intron-variant	MED16	GRCh38.p7	19:887472	GGAGTTCGACACCAT[C/T]CTGGCCAAGATAGTG	10025
rs62132325	snp	C/G			intron-variant	MED16	GRCh38.p7	19:889951	GCACAAGGCGCACTC[C/G]AGAGATGCCCTGAGA	10025
rs67796778	snp	C/T	0.499977	0.00339449	intron-variant	MED16	GRCh38.p7	19:879545	TGCCTACCAGGGCCA[C/T]GCCCCAGCAGCTCGC	10025
rs71335318	in-del	-/C	0.5	0	intron-variant	MED16	GRCh38.p7	19:874156	CTCACTCTGTCGCCC[-/C]AGGCTGGAGTGCAGT	10025
rs71952964	in-del	-/CACGCCTGCA	0.320335	0.239902	intron-variant	MED16	GRCh38.p7	19:882387	TGTGTGGTGGTGATG[-/CACGCCTGCA]CACGCCTGTAGTCCC	10025
rs72298146	in-del	-/TCTCCAGGCCCCGCACCGATAACCCCGCAG	0.398174	0.201356	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:892656	AGGGACCCTATTCCC[lengthTooLong]TCTCCAGGCCCTGCC	10025
rs72306990	in-del	-/GCCCCGAGCCCCGCGCCCCGC			intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:892875	CGCCGCAAACCCTGA[-/GCCCCGAGCCCCGCGCCCCGC]GCCCCGCGCCCCGCG	10025
rs72984029	snp	A/G	0.102253	0.20167	intron-variant	MED16	GRCh38.p7	19:871033	AATGCAGGGACACAC[A/G]CACCTGGCGAGGCCG	10025
rs72984030	snp	A/G	0.0722242	0.175772	intron-variant	MED16	GRCh38.p7	19:871604	AGACAGCAAACAGGT[A/G]CCTGGAAGTGGCTGC	10025
rs72984031	snp	A/G	0.345989	0.230838	synonymous-codon	MED16	GRCh38.p7	19:872089	GGTGCCGTCCCGCAG[A/G]AAGCTGTGGCCCGGC	10025
rs72984032	snp	C/T	0.000154431	0.00878587	missense, intron-variant	MED16	GRCh38.p7	19:877009	GGCGCGTGTACTCCT[C/T]GTGCAGCTTCTCCAC	10025
rs72984035	snp	C/T	0.499977	0.00339449	intron-variant	MED16	GRCh38.p7	19:879534	CTGGTTGTCAATGCC[C/T]ACCAGGGCCACGCCC	10025
rs72984044	snp	G/T	0.00636936	0.0560724	intron-variant	MED16	GRCh38.p7	19:889407	GCCACTGAACACGCA[G/T]GTGCCAATGACAGCC	10025
rs73492565	snp	A/G	0.0109702	0.0732444	intron-variant	MED16	GRCh38.p7	19:868329	GCAGCCGGGCTCAGG[A/G]GCAGCTGAGGGGTAG	10025
rs73492568	snp	A/G	0.362941	0.223034	intron-variant	MED16	GRCh38.p7	19:871724	GGCTTATGTTCTGGC[A/G]GGGGGCTCAGGCAGG	10025
rs73492573	snp	C/T	0.5	0	intron-variant	MED16	GRCh38.p7	19:877493	AACAGCTCCTAGTTA[C/T]GAAGCTCCTAATACG	10025
rs73492577	snp	C/T	0.409721	0.192325	intron-variant	MED16	GRCh38.p7	19:885118	TGCTGGGCCTGTCTC[C/T]TCAGCCACGCCTGCC	10025
rs73492579	snp	A/G	0.0448719	0.142907	intron-variant	MED16	GRCh38.p7	19:885268	CAAGTCAGGGGCTTC[A/G]AGGAGTTTGGGGCGT	10025
rs73492585	snp	G/T	0.0429648	0.14013	intron-variant	MED16	GRCh38.p7	19:886637	GGCCCTGGGCCGCAC[G/T]GTGCAGACCTGAGCT	10025
rs73492587	snp	C/T	0.0429648	0.14013	intron-variant	MED16	GRCh38.p7	19:887013	GAATCCAGGAGGTGG[C/T]GATTGCAGTGAGCCG	10025
rs73492588	snp	A/G	0.0429648	0.14013	intron-variant	MED16	GRCh38.p7	19:887042	CGAGATCACACCATT[A/G]CACTCTGGCCTGGGC	10025
rs73492592	snp	A/G	0.0429648	0.14013	intron-variant	MED16	GRCh38.p7	19:888774	TGCTGCGTGTACTGC[A/G]GCAATGCGCCGACAA	10025
rs73492593	snp	A/G	0.0429648	0.14013	intron-variant	MED16	GRCh38.p7	19:888929	GCTGGGGTGGCTGTG[A/G]GGCCTTTGCCACGAA	10025
rs73505576	snp	A/G	0.0429648	0.14013	intron-variant	MED16	GRCh38.p7	19:888993	GACACACAGAGGTGA[A/G]GAGTCAGAGCCTGAA	10025
rs73505578	snp	A/C	0.0433465	0.140692	intron-variant	MED16	GRCh38.p7	19:889216	CCACGCCTACTCTTA[A/C]CTGTGGGGCCGAATC	10025
rs73505579	snp	A/T	0.0429648	0.14013	intron-variant	MED16	GRCh38.p7	19:889316	GCCACCAGTTATACA[A/T]GCAGCTACCTAAGGA	10025
rs73505582	snp	C/T	0.0429648	0.14013	intron-variant	MED16	GRCh38.p7	19:889361	GAAAGAGATAACTCA[C/T]TAAGAACGGCCACCC	10025
rs73505584	snp	A/G	0.0429648	0.14013	intron-variant	MED16	GRCh38.p7	19:889404	GGGGCCACTGAACAC[A/G]CAGGTGCCAATGACA	10025
rs73505588	snp	A/G	0.0291086	0.117077	intron-variant	MED16	GRCh38.p7	19:890295	CCACAGCCTGCAGAC[A/G]ATGACGATGACTCCA	10025
rs73505589	snp	C/T	0.0444908	0.142359	intron-variant	MED16	GRCh38.p7	19:890637	CGGGCACAGCCACCA[C/T]GCACCTTTCAAAAAC	10025
rs73505590	snp	C/T	0.0429648	0.14013	intron-variant	MED16	GRCh38.p7	19:890735	AGCCCGATTCGATCC[C/T]GCACACGGGGCGATC	10025
rs73505593	snp	G/T	0.0652144	0.168387	intron-variant	MED16	GRCh38.p7	19:890881	AGAGACCGAGTCCCT[G/T]CAAGGCAGTGGGCCG	10025
rs73505595	snp	G/T	0.0119582	0.0763945	intron-variant	MED16	GRCh38.p7	19:891156	CACCAGCTCCTGCGG[G/T]AGGGAGGTGTGGTGG	10025
rs73505596	snp	C/G	0.0429648	0.14013	intron-variant	MED16	GRCh38.p7	19:891334	GAGGTCAGGGCCAGT[C/G]CTGGGCCTGTGGGCT	10025
rs73505597	snp	A/C	0.0429648	0.14013	intron-variant	MED16	GRCh38.p7	19:891372	TCAGTAAGGTGGGAG[A/C]CCGGGAGGGCTGGGA	10025
rs73505599	snp	C/G	0.0429648	0.14013	intron-variant	MED16	GRCh38.p7	19:891395	GGCTGGGACCTATTT[C/G]GGTTTCACCAGGACC	10025
rs73505601	snp	A/C/T	0.5	0	upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:893481	TGGTGGAACTCAATA[A/C/T]TCGTGCTCGCTTCGG	10025
rs73919872	snp	A/G	0.0142736	0.0832652	intron-variant	MED16	GRCh38.p7	19:870039	GGTTGCCCAAACCCC[A/G]CACATTCCAGAGAAA	10025
rs73919887	snp	A/C	0.001252	0.0249887	intron-variant	MED16	GRCh38.p7	19:873435	GCGGGGCCTTAGGGG[A/C]GAGCATGGCGCACCT	10025
rs74372962	snp	C/G	0.5	0	intron-variant	MED16	GRCh38.p7	19:878493	CCCCTGGCTGTCAAT[C/G]CCCACCAGCCCCAGC	10025
rs74394387	snp	C/T	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:882899	GGGTCCTGTGAGCAG[C/T]ATTCCCTGGGGGGAA	10025
rs74595566	snp	A/G	0.093417	0.194889	intron-variant	MED16	GRCh38.p7	19:873832	CCTGCAGGCCTTGGC[A/G]TGGGCAGGTCCCCAT	10025
rs74669729	snp	A/C	0.5	0	intron-variant	MED16	GRCh38.p7	19:887665	AACAAGACTCTGTCT[A/C]AAAAAAAATGTATTT	10025
rs74697243	snp	A/T	0.0182019	0.0936463	intron-variant	MED16	GRCh38.p7	19:875014	CTAAAAATACAAAAA[A/T]TCAGCCGGGCGTGGT	10025
rs74707923	in-del	-/AA			intron-variant	MED16	GRCh38.p7	19:880934	CAACTCAAAAAAAAA[-/AA]GAAAAAAAAAAATAG	10025
rs75057096	snp	A/G	0.0174175	0.0916809	intron-variant	MED16	GRCh38.p7	19:869652	CTTCCCGGAGGTCCC[A/G]GAGCCAAGCCGGGGG	10025
rs75080491	snp	A/G	0.00478085	0.0486577	intron-variant	MED16	GRCh38.p7	19:890407	ACAGGCTGTCCCCCC[A/G]CAGGAACAGAGCAGG	10025
rs75296500	snp	A/C			intron-variant	MED16	GRCh38.p7	19:871884	GGGGAGAGGGGAGAG[A/C]GGGGAGCGGGGAGAG	10025
rs75472463	snp	C/G	0.5	0	intron-variant	MED16	GRCh38.p7	19:873157	GGTGGGGCAGGGCTA[C/G]GAAGTGGGGCAGGGC	10025
rs75518805	snp	A/T	0.5	0	upstream-variant-2KB, nc-transcript-variant	MED16, RNU6-9	GRCh38.p7	19:893585	CGTGAAGCGTTCCAT[A/T]TTTTTTTTTTTTTTT	10025
rs75703478	snp	A/C	0.0182019	0.0936463	intron-variant	MED16	GRCh38.p7	19:875016	AAAAATACAAAAAAT[A/C]AGCCGGGCGTGGTGG	10025
rs75794867	snp	A/G	0.5	0	intron-variant	MED16	GRCh38.p7	19:873125	GGGCAGGGCTCCGAG[A/G]TGGGGCAGGGCTCCG	10025
rs75932399	snp	C/G	0.226779	0.248919	intron-variant	MED16	GRCh38.p7	19:873175	AGTGGGGCAGGGCTA[C/G]GAAGTGGGGCAGGGC	10025
rs76092252	snp	C/G	0.109685	0.207674	intron-variant	MED16	GRCh38.p7	19:869700	CTGGAGCCGAGCCGG[C/G]GCCTTCCCCGGAGCA	10025
rs76224149	snp	A/C	0.5	0	intron-variant	MED16	GRCh38.p7	19:873156	AGGTGGGGCAGGGCT[A/C]GGAAGTGGGGCAGGG	10025
rs76277763	snp	A/G	0.0429648	0.14013	intron-variant	MED16	GRCh38.p7	19:890310	GATGACGATGACTCC[A/G]GGCAGGCTCCAGGTA	10025
rs76403059	snp	A/C/G	0.00700503	0.0588435	missense, synonymous-codon	MED16	GRCh38.p7	19:879943	GCAGCTCACCTTCCC[A/C/G]TGGCTGTCAATCCCC	10025
rs76464663	snp	A/G			intron-variant	MED16	GRCh38.p7	19:879591	AATGCCCAGCAGCTC[A/G]CCTTCCCGTGGTTGT	10025
rs76526124	snp	C/T	0.00953873	0.0683987	upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:893298	AATTCCCAGCAGCCA[C/T]CGTAGCTATATTTGG	10025
rs76542322	snp	A/G	0.5	0	intron-variant	MED16	GRCh38.p7	19:873178	GGGGCAGGGCTAGGA[A/G]GTGGGGCAGGGCTAG	10025
rs76595966	snp	A/C	0.5	0	intron-variant	MED16	GRCh38.p7	19:873174	AAGTGGGGCAGGGCT[A/C]GGAAGTGGGGCAGGG	10025
rs76596016	snp	A/G	0.0429648	0.14013	intron-variant	MED16	GRCh38.p7	19:887101	AAAAAAAAAAAGAAC[A/G]AGAAAAATGTCTCTA	10025
rs76653066	snp	A/G	0.00953873	0.0683987	intron-variant	MED16	GRCh38.p7	19:890708	CAACAAGCCTCCGTC[A/G]ACCAACGCTCCAGCC	10025
rs76711088	snp	A/C/T	0.00489618	0.049236	intron-variant	MED16	GRCh38.p7	19:871651	ACACAGAGCATGGAC[A/C/T]TGTGCTAGGAACTGG	10025
rs76960739	snp	A/G	0.00716266	0.059414	intron-variant	MED16	GRCh38.p7	19:870620	CTGGGTGCCCGTGTT[A/G]GGGGTGGTTCGTGAC	10025
rs77020164	snp	C/T	0	0	upstream-variant-2KB, downstream-variant-500B	MED16, RNU6-9	GRCh38.p7	19:893600	ATTTTTTTTTTTTTT[C/T]CCATTTTCCCTCCCA	10025
rs77196903	snp	A/G	0.000894588	0.0211304	intron-variant	MED16	GRCh38.p7	19:868952	GCCTGGGGCCCTGGC[A/G]GGAGAGGGGAGAACG	10025
rs77249256	snp	A/G	0.0110488	0.0735005	intron-variant	MED16	GRCh38.p7	19:875228	CTCGAGGCCCCGGGC[A/G]TGGAAAAGGACCCAC	10025
rs77396633	snp	A/G	0.00953873	0.0683987	intron-variant	MED16	GRCh38.p7	19:887771	ATGCCAGACACAGAA[A/G]GCTACGCAGTGTGTG	10025
rs77743959	snp	A/C/T	0.0490535	0.14873	intron-variant	MED16	GRCh38.p7	19:873774	CCCACTGCCTGCCCC[A/C/T]CCCCGGGGGCCGCTG	10025
rs77750649	snp	A/C	0.5	0	intron-variant	MED16	GRCh38.p7	19:887666	ACAAGACTCTGTCTC[A/C]AAAAAAATGTATTTG	10025
rs77786764	snp	C/T	0.0581099	0.160244	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:892307	CCTGACCCCCTTTGC[C/T]TCCCACACTTCATTT	10025
rs77924290	snp	A/G	0.00560509	0.0526415	missense, utr-variant-5-prime	MED16	GRCh38.p7	19:891119	CTGCCGCTGGCCGCC[A/G]CAAATCACACATGAG	10025
rs77968665	snp	A/G	0.00914312	0.0669923	intron-variant	MED16	GRCh38.p7	19:874603	CAGGACCCGGGTGCC[A/G]GGTGTCGGCCTGGGA	10025
rs78047294	snp	A/G	0.320873	0.239752	synonymous-codon	MED16	GRCh38.p7	19:871987	GTCCTGGGTATCCGA[A/G]GTGGCCGTATACACG	10025
rs78057637	snp	C/T	0.00107623	0.0231724	intron-variant	MED16	GRCh38.p7	19:872136	GCCCGAAAGAGGCAT[C/T]GGTGTGGCTGGGGCG	10025
rs78093369	snp	C/G	0	0	intron-variant	MED16	GRCh38.p7	19:872987	GGCTCCGAGGTGGGG[C/G]AGGGCTCCGAGGTGG	10025
rs78105938	snp	A/G	0.5	0	intron-variant	MED16	GRCh38.p7	19:873160	GGGGCAGGGCTAGGA[A/G]GTGGGGCAGGGCTAG	10025
rs78140937	snp	C/T	0.00835141	0.0640778	intron-variant	MED16	GRCh38.p7	19:883724	AGACACAGACGTGCC[C/T]AGCGGGGGCACCGGG	10025
rs78469799	snp	A/T	0.00159617	0.0282053	upstream-variant-2KB, nc-transcript-variant	MED16, RNU6-9	GRCh38.p7	19:893586	GTGAAGCGTTCCATA[A/T]TTTTTTTTTTTTTTC	10025
rs78579800	snp	A/G	0.0279526	0.114869	intron-variant	MED16	GRCh38.p7	19:881485	AGCTCCCACGACCCC[A/G]TGGCCTGTGCTCAGG	10025
rs78700964	snp	A/C/T	0.00478085	0.0486577	intron-variant	MED16	GRCh38.p7	19:868751	ACACTCCCTCTGGGA[A/C/T]GTGCTCCCTCCACCA	10025
rs79264833	snp	A/G	0.0267878	0.112589	intron-variant	MED16	GRCh38.p7	19:870109	GGAGATCCTCCTGAT[A/G]AGGTGTCTGCTCAGC	10025
rs79354198	snp	G/T	0.00244167	0.034855	intron-variant	MED16	GRCh38.p7	19:868507	AGCCGCACCTGCGGG[G/T]AGGCAGGCACTGAGC	10025
rs79505764	snp	C/G/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:874554	GCCTCAGTCCCCTTA[C/G/T]GGCAAAACGGAAGGA	10025
rs79512329	snp	A/G	0.0168055	0.0901129	intron-variant	MED16	GRCh38.p7	19:875663	TTCTCAGCTGGGAGC[A/G]GCTCTGCCTCTGGTG	10025
rs79931316	snp	C/T	0.0429648	0.14013	intron-variant	MED16	GRCh38.p7	19:887117	AGAAAAATGTCTCTA[C/T]GTTGTGAAAAAATGC	10025
rs79961155	snp	G/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:876547	GCTTAACGTGTTACA[G/T]AAGAAACTTCCCAGG	10025
rs79979039	snp	C/G	0	0	intron-variant	MED16	GRCh38.p7	19:879428	GTCAATGCCCACCAA[C/G]CCCAGCCCCACGTGC	10025
rs80114377	snp	A/G	0.0452528	0.143452	intron-variant	MED16	GRCh38.p7	19:888744	CCCCGGAGGGCCCCC[A/G]TGGCACGAAGCCGGT	10025
rs80126239	snp	A/G	0.00517822	0.0506191	intron-variant	MED16	GRCh38.p7	19:869002	ACGAGGCCAGGTTCC[A/G]GCAGGGGCATCTGTC	10025
rs80174077	snp	C/T	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:883838	ACTCACCACGAGGCC[C/T]AGGGGAAGGAATGAG	10025
rs80283045	snp	A/C	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:874036	GTCCCACAGAACTAA[A/C]CATGACTGTGCACAC	10025
rs80314410	snp	A/G	0.021333	0.101051	intron-variant	MED16	GRCh38.p7	19:872927	CAGCAGAGGCTTCAT[A/G]GAGAGGAGGGCTCCG	10025
rs80331571	snp	A/G	0.0236746	0.106192	intron-variant	MED16	GRCh38.p7	19:891190	GTCTATGTTGGCTGA[A/G]CACCCAGGGCATGTG	10025
rs111267130	snp	C/T			intron-variant	MED16	GRCh38.p7	19:879355	CTCACCTTCCCCTGG[C/T]TGTCAATGCCCACCA	10025
rs111279457	snp	A/G	0.00914312	0.0669923	intron-variant	MED16	GRCh38.p7	19:883931	CCTCTTCACCTGCCT[A/G]GTGACTCACTACAAG	10025
rs111310751	snp	C/G	0.363776	0.222609	intron-variant	MED16	GRCh38.p7	19:878159	GCAGCTCACCTTCCC[C/G]TGGTTGTCAATGCCC	10025
rs111361713	snp	C/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:877486	TCCTCTCAACAGCTC[C/G]TAGTTACGAAGCTCC	10025
rs111469573	snp	A/C	0.178144	0.239451	intron-variant	MED16	GRCh38.p7	19:876882	ACCTGCCACGGGGCC[A/C]CCACCTGCCACGGGG	10025
rs111500285	snp	A/G	0.118584	0.212673	upstream-variant-2KB	MED16	GRCh38.p7	19:894754	ACATAGCCAGACCCC[A/G]TCTCTACAAAAAAAA	10025
rs111502305	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:891762	GGAACACCTGTGGCC[A/G]AGGCGGGGGCTGAGT	10025
rs111513773	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:891874	GGAACACCTGTGGCC[A/G]AGGCGGGGGCTGAGT	10025
rs111532824	snp	A/C			intron-variant	MED16	GRCh38.p7	19:878821	GTGCCCCAGCAGCTC[A/C]CCTTCCCCTGGTTGT	10025
rs111542276	snp	A/G	0.0460142	0.144533	intron-variant	MED16	GRCh38.p7	19:886936	ACAAAAAAATTAGCC[A/G]GGCATGGTAGCGGGT	10025
rs111573124	snp	G/T			intron-variant	MED16	GRCh38.p7	19:877620	GTCCCTTCCCCCGGG[G/T]GCGCCTCCCTCTGGC	10025
rs111620646	snp	C/T	0.5	0	utr-variant-3-prime	MED16	GRCh38.p7	19:868049	GTGAGGCAAGGAAAC[C/T]GAGGAGACGCCCGAG	10025
rs111755884	snp	A/T	0.5	0	downstream-variant-500B	MED16	GRCh38.p7	19:867750	AAGGCAGATGCCTGG[A/T]CAGAAGCCACCCTGA	10025
rs111756427	snp	A/G	0.5	0	intron-variant	MED16	GRCh38.p7	19:879255	ATGCCCCAGCAGCTC[A/G]CCTTCCTCTGGTTGT	10025
rs111761152	snp	A/G	0.00159617	0.0282053	intron-variant	MED16	GRCh38.p7	19:873370	GAGGTGGTTTTGAGG[A/G]GCAGGGGCAGGGAAG	10025
rs111830851	snp	A/G	0.0429648	0.14013	intron-variant	MED16	GRCh38.p7	19:887523	ATACAAAAATTAGCC[A/G]GGCGCGGTGGTGCGT	10025
rs111843049	snp	C/T	0.0437281	0.141251	intron-variant	MED16	GRCh38.p7	19:876357	TCTCCTTCCGACGGG[C/T]GGGTCTCTGTGTGTT	10025
rs111913726	snp	C/T	0.00478085	0.0486577	intron-variant	MED16	GRCh38.p7	19:884189	CGGGAAAACATCTCC[C/T]TTCTCCAGAGCGGAG	10025
rs111940149	snp	A/G	0.0168687	0.0902763	synonymous-codon	MED16	GRCh38.p7	19:875380	CTTGGTGTGGTAGTC[A/G]CACACGCGGGTCACC	10025
rs111955506	snp	C/T	0.5	0	intron-variant	MED16	GRCh38.p7	19:887517	CTAAAAATACAAAAA[C/T]TAGCCGGGCGCGGTG	10025
rs112009126	snp	A/G	0.5	0	intron-variant	MED16	GRCh38.p7	19:888712	AGACAAACGGGGACC[A/G]CAGGGTGGGGAGTGC	10025
rs112016758	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:882300	ATGGCTTGAGTCCAG[A/G]AGTTCAAGACCAGCC	10025
rs112050406	snp	A/G	0.0183953	0.0941236	intron-variant	MED16	GRCh38.p7	19:890092	GGGCCCCCCTGCTCC[A/G]GGATCCGGGTCGCCA	10025
rs112061574	snp	C/T	0.0588605	0.161139	downstream-variant-500B	MED16	GRCh38.p7	19:867661	ATACACAGAGAAGTG[C/T]AGAGATACCAGAGAC	10025
rs112066565	snp	C/T			intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:891669	GGCGGGGGCTGAGTG[C/T]GACGGGGAACACCTG	10025
rs112167623	snp	A/G	0	0	intron-variant	MED16	GRCh38.p7	19:884739	TGCTGGCAGGCGCGC[A/G]GTCACACCCGAGATC	10025
rs112174955	snp	A/G			intron-variant	MED16	GRCh38.p7	19:884216	GGAGGCCAGCCTAAA[A/G]ACCAGGCCCGCAGCC	10025
rs112193872	snp	C/T	0.5	0	intron-variant	MED16	GRCh38.p7	19:883416	GACCGAAGCCTGGCA[C/T]GGTGGGCACGTGGGG	10025
rs112202451	snp	A/G	0.5	0	intron-variant	MED16	GRCh38.p7	19:889581	GAGGGGCTGGCGGGT[A/G]GCTGGGTAGGGTGAC	10025
rs112204210	snp	A/G	0.5	0	intron-variant	MED16	GRCh38.p7	19:879483	TGTCAATGCCCACCA[A/G]CCCCAGCCCCACGTG	10025
rs112248526	snp	C/T			intron-variant	MED16	GRCh38.p7	19:877700	GCCTTCCCCTGGTTG[C/T]CAATGCCCACCAGCC	10025
rs112251710	snp	C/T	0.0232847	0.105357	intron-variant	MED16	GRCh38.p7	19:889992	AAGAATGATTCGGGC[C/T]ACTATGGAAAGAGCA	10025
rs112354760	snp	C/T	2.06052e-05	0.0032097	synonymous-codon, utr-variant-5-prime	MED16	GRCh38.p7	19:886148	GCCGAACAGCGTGAG[C/T]GACGGTGAGAACTTG	10025
rs112395844	snp	A/C/T	0.000286779	0.0119714	intron-variant	MED16	GRCh38.p7	19:884891	GGCCTCCGCAGCCGG[A/C/T]GGGAGACTCACCCAC	10025
rs112403977	snp	A/G	0.212728	0.247206	intron-variant	MED16	GRCh38.p7	19:871799	GGAGAGCGGGGAGAA[A/G]GGAGAGCGGGGAGAG	10025
rs112427239	in-del	-/CTC	0.5	0	intron-variant	MED16	GRCh38.p7	19:886381	CTGACCCTCCGTCTC[-/CTC]ATCTGTAAGGTGGAA	10025
rs112438061	snp	A/T	0.0441095	0.141807	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:892042	GCGGGGCTGAGTGTG[A/T]TGGGGAACACCTGTG	10025
rs112466570	snp	A/G	0.122758	0.215196	upstream-variant-2KB	MED16	GRCh38.p7	19:894324	CAGGCGTGAGCCACC[A/G]CGCCCAGCCTGTTTT	10025
rs112502061	snp	A/C	0.0205511	0.0992634	downstream-variant-500B	MED16	GRCh38.p7	19:867834	ACTTTGGATACCCCC[A/C]GACTCGGCATCCACT	10025
rs112509997	snp	C/T	0.00279162	0.0372561	intron-variant	MED16	GRCh38.p7	19:872725	AGGTGGAGGTGTGGA[C/T]GGAGACTTGATTTCA	10025
rs112523035	snp	C/T	0.320335	0.239902	intron-variant	MED16	GRCh38.p7	19:876910	GGGCCCCACCTGCCA[C/T]GGGGCCCCCACCTGC	10025
rs112530485	in-del	-/AGGGGCTGGCG/AGGGGCTGGCGAGGGGCTGGCGAGGGGCTGGCG	0.0123036	0.0774623	intron-variant	MED16	GRCh38.p7	19:877576	CAAGGCAGCGCAGGC[lengthTooLong]AGGGGCTGGCGAGGG	10025
rs112539899	snp	A/C/G			intron-variant	MED16	GRCh38.p7	19:871838	GGGGAGAGGGGAGAG[A/C/G]GGGGAGAGGGGAGAG	10025
rs112552099	snp	C/G	0.0429648	0.14013	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:892678	GCCCCGCACCGATAA[C/G]CCCGCAGTCTCCAGG	10025
rs112556341	snp	C/T	0.0232847	0.105357	intron-variant	MED16	GRCh38.p7	19:882869	AGAGCCTTGACCTCC[C/T]GCAAACCCGTATAGG	10025
rs112560510	snp	A/C/G/T	0.00690115	0.0583933	intron-variant	MED16	GRCh38.p7	19:868540	GTTCCCACTTCCAGG[A/C/G/T]GGGCCTCCCTTACGC	10025
rs112590622	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:877371	GCACAATGCCTCTGG[A/G]AACAGGGAAGGAAAC	10025
rs112649089	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:890724	ACCAACGCTCCAGCC[C/T]GATTCGATCCCGCAC	10025
rs112659372	snp	C/T	0.0429648	0.14013	intron-variant	MED16	GRCh38.p7	19:888741	GCACCCCGGAGGGCC[C/T]CCGTGGCACGAAGCC	10025
rs112703975	snp	C/T	0.0176183	0.0921886	intron-variant	MED16	GRCh38.p7	19:873601	CAAGGAGACGTGGGT[C/T]GGGTCAGCTCGGGCC	10025
rs112706448	snp	C/T	3.37541e-05	0.00410803	synonymous-codon	MED16	GRCh38.p7	19:868472	CGTGGTTCTGTTGGG[C/T]GACTTGAGCATGGTG	10025
rs112712001	snp	C/T	0.00676609	0.0577691	intron-variant	MED16	GRCh38.p7	19:887727	GCCACAGCGGGGATG[C/T]ACCTTGAGGACATCA	10025
rs112714425	snp	A/G	0.0425331	0.13949	intron-variant	MED16	GRCh38.p7	19:873057	AGGGCTCCGAGGTGG[A/G]GCAGGGCTCCGAGGT	10025
rs112762747	snp	A/G			intron-variant	MED16	GRCh38.p7	19:872658	GTGTACCGGCGGGGG[A/G]GTGGGGGCGAGGTTG	10025
rs112788143	snp	C/T			intron-variant	MED16	GRCh38.p7	19:877836	CCGTGGTTGTCAATG[C/T]CCACCAAGCCCAGCC	10025
rs112800475	snp	C/T	0.5	0	upstream-variant-2KB	MED16	GRCh38.p7	19:894588	TCTCCAAGAGGGCCA[C/T]GCAGTGACCTTACAG	10025
rs112839858	in-del	-/CT	0.386123	0.209692	intron-variant	MED16	GRCh38.p7	19:877295	TGTGCGCGCACGCCC[-/CT]GTGTGTGGGCCTGTG	10025
rs112844899	snp	C/T			intron-variant	MED16	GRCh38.p7	19:879046	CAGCTCACCTTCCCC[C/T]GGTTGTCAATGCCCA	10025
rs112855098	snp	A/G	0.00953873	0.0683987	upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:893415	CTAGGTCATTTAAGA[A/G]AAGTCGGCCTATGTG	10025
rs113015819	snp	C/T	0.0429648	0.14013	intron-variant	MED16	GRCh38.p7	19:887900	ACTGGGTTTCCTTTT[C/T]GGGTGATGAGAAGGG	10025
rs113031277	snp	C/G	0.00397779	0.0444193	intron-variant	MED16	GRCh38.p7	19:872951	GGCTCCGAGGTGGGG[C/G]AGGGCTCCGAGGTGG	10025
rs113032095	snp	C/T	0.5	0	intron-variant	MED16	GRCh38.p7	19:868364	GGAGTAGCTGAGGGG[C/T]AGCTGGGCTCAGGGG	10025
rs113040541	snp	C/T	0.5	0	intron-variant	MED16	GRCh38.p7	19:883357	GACCGAAGCCTGGCA[C/T]GGTGGGCACGTGGGG	10025
rs113084303	snp	C/G			intron-variant	MED16	GRCh38.p7	19:879463	GCAGCTCGCCTTCCC[C/G]TGGTTGTCAATGCCC	10025
rs113099646	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:877330	CGCATGTGTCTGTAG[C/T]GTCTGTACCTTTCTG	10025
rs113179184	snp	C/G			missense	MED16	GRCh38.p7	19:871970	AAGAGCAGGGACATG[C/G]TGTCCTGGGTATCCG	10025
rs113193194	snp	A/G	0.0429648	0.14013	intron-variant	MED16	GRCh38.p7	19:886800	TGGGGTCTTGGCTGC[A/G]CACGGTGGCTCTCGC	10025
rs113251429	snp	A/G			intron-variant	MED16	GRCh38.p7	19:878785	CCCCTGGTTGTCAAT[A/G]CCCACCAGCCCCAGC	10025
rs113251487	snp	A/G	0.5	0	intron-variant	MED16	GRCh38.p7	19:878115	CCACGTGCCCCAGCA[A/G]CTCACCTTCCCCTGG	10025
rs113315843	snp	C/T	0.5	0	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:891931	CGGGGCTGAGTGTGA[C/T]GGGGAACACCTGTGG	10025
rs113323399	snp	C/T	0	0	intron-variant	MED16	GRCh38.p7	19:878124	CCAGCAACTCACCTT[C/T]CCCTGGTTGTCAATG	10025
rs113332652	snp	A/G	0.0184827	0.0943384	intron-variant	MED16	GRCh38.p7	19:890099	CCTGCTCCGGGATCC[A/G]GGTCGCCACCCCTGG	10025
rs113348883	snp	A/G	0.0887219	0.191022	intron-variant	MED16	GRCh38.p7	19:882396	GTGATGCACGCCTGC[A/G]CACGCCTGTAGTCCC	10025
rs113373803	snp	G/T			intron-variant	MED16	GRCh38.p7	19:872443	ACAGCTGCGGGCCCG[G/T]GCCCCTGGTGACTGT	10025
rs113415855	snp	A/G	0.0429648	0.14013	intron-variant	MED16	GRCh38.p7	19:886621	CAGGCGGGGGCCGTC[A/G]GGCCCTGGGCCGCAC	10025
rs113421264	snp	A/G	0	0	intron-variant	MED16	GRCh38.p7	19:876894	GCCCCCACCTGCCAC[A/G]GGGCCCCACCTGCCA	10025
rs113435198	snp	C/T	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:874155	GTCTCACTCTGTCGC[C/T]CAGGCTGGAGTGCAG	10025
rs113482685	snp	C/G			intron-variant	MED16	GRCh38.p7	19:877292	TCTGTGTGCGCGCAC[C/G]CCCGTGTGTGGGCCT	10025
rs113485901	snp	C/T	0.5	0	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:892488	GTACTCTCCAGGCCC[C/T]TCCCCTATTGCCCCC	10025
rs113696681	snp	A/C			intron-variant	MED16	GRCh38.p7	19:871790	GGGGAGAGGGGAGAG[A/C]GGGGAGAAGGGAGAG	10025
rs113705969	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:891560	CGCAGACAGGCAAGC[A/G]GTGGGGCGGCTCCCT	10025
rs113717112	snp	C/T	0.0429648	0.14013	intron-variant	MED16	GRCh38.p7	19:891455	GGGCCAAGGGCACAG[C/T]CGGGAGACGCAGCGG	10025
rs113736860	snp	A/C/G			intron-variant	MED16	GRCh38.p7	19:871854	GGGGAGAGGGGAGAG[A/C/G]GGGGAGCGGGGAGCG	10025
rs113800228	snp	A/G	0.00953873	0.0683987	intron-variant	MED16	GRCh38.p7	19:889503	GTGCTAATGACAGCC[A/G]GACTGCAGGTGGGAG	10025
rs113801603	snp	C/T	0.0193772	0.0965046	intron-variant	MED16	GRCh38.p7	19:887719	TGACTCAGGCCACAG[C/T]GGGGATGCACCTTGA	10025
rs113805600	snp	C/G	0.0429648	0.14013	intron-variant	MED16	GRCh38.p7	19:889275	TGTTACTAAATCAGA[C/G]GGTGGGCTGCATTCA	10025
rs113862234	snp	C/T	0.0670745	0.170406	utr-variant-3-prime	MED16	GRCh38.p7	19:868031	GTTCAGCGCTCTCCG[C/T]GGGTGAGGCAAGGAA	10025
rs113924929	snp	A/C	0	0	intron-variant	MED16	GRCh38.p7	19:878765	GTGCCCCAGCAGCTC[A/C]CCTTCCCCTGGTTGT	10025
rs113953058	snp	C/T	0.5	0	upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:893483	GTGGAACTCAATATT[C/T]GTGCTCGCTTCGGCA	10025
rs114066375	snp	A/G	0.0138799	0.0821421	intron-variant	MED16	GRCh38.p7	19:887273	GGTTGCCATGGCGAC[A/G]ACTCATCTGGTGTCC	10025
rs114186621	snp	A/C	0.0263992	0.111815	intron-variant	MED16	GRCh38.p7	19:873930	TGTGAACACAGGGGC[A/C]TGTCCACAGCGTGCA	10025
rs114201442	snp	C/T	0.00914312	0.0669923	intron-variant	MED16	GRCh38.p7	19:890678	CACCGTCTAGAAAAC[C/T]GGGGCACGTGTCTCC	10025
rs114303076	snp	C/T	0.0444908	0.142359	intron-variant	MED16	GRCh38.p7	19:869416	AGCTGCCCTCGGTGG[C/T]GGGTGGGGGACCTGG	10025
rs114345288	snp	A/C	0.0197687	0.0974348	intron-variant	MED16	GRCh38.p7	19:883025	AACTCAACGCCCCAG[A/C]GCCGGGGGAGGCAGC	10025
rs114359895	snp	C/T	0.0117958	0.0758865	intron-variant	MED16	GRCh38.p7	19:868503	ACACAGCCGCACCTG[C/T]GGGGAGGCAGGCACT	10025
rs114474315	snp	C/T	0.00755907	0.0610114	intron-variant	MED16	GRCh38.p7	19:886735	TTTGTCAAGTCATTA[C/T]TGACATACGGAAACA	10025
rs114495755	snp	A/G	0.000123591	0.00786003	synonymous-codon	MED16	GRCh38.p7	19:885986	GATGTTGCCGCCGCC[A/G]GTGAAGGCGATGTCG	10025
rs114514299	snp	C/G	0.00795532	0.062565	intron-variant	MED16	GRCh38.p7	19:886375	TCCCCTCTGACCCTC[C/G]GTCTCCTCATCTGTA	10025
rs114593583	snp	C/G/T	0.031825	0.122064	intron-variant	MED16	GRCh38.p7	19:885455	CGGGAGAGCACGTTG[C/G/T]GGGGGGTCCGGGGGC	10025
rs114607709	snp	A/G	0.0482946	0.147699	intron-variant	MED16	GRCh38.p7	19:870515	GCAGTGGGCCAAGAC[A/G]GCACTACTGCACTCC	10025
rs114768563	snp	A/G	0.00246002	0.0349851	intron-variant	MED16	GRCh38.p7	19:890466	AAACCAGATTAGAAG[A/G]AAATGACTCCGAAAT	10025
rs114827759	snp	A/G	0.00914312	0.0669923	intron-variant	MED16	GRCh38.p7	19:874833	TGGGACTGCGTCACC[A/G]TGCTGCAACCTGGAT	10025
rs114851848	snp	C/G	0.00358779	0.0422022	intron-variant	MED16	GRCh38.p7	19:870070	GGCCAGCCCCGGGCC[C/G]TGCAAGGTGACCTCT	10025
rs114852161	snp	A/G	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:884362	CCGTGGGTGCGGGGG[A/G]CCCATCGGGCGGATA	10025
rs115005219	snp	A/G	0.00993419	0.0697739	intron-variant	MED16	GRCh38.p7	19:887826	ACAGGCAGATCCAGA[A/G]AGACAACTGGGTCTC	10025
rs115411488	snp	A/G	0.0410537	0.137264	intron-variant	MED16	GRCh38.p7	19:875909	TCCTGGAGGCTGGGA[A/G]TTGGAGAGCCTGTGC	10025
rs115647802	snp	C/T	0.0252325	0.109451	intron-variant	MED16	GRCh38.p7	19:881478	TGGTGTGAGCTCCCA[C/T]GACCCCGTGGCCTGT	10025
rs115650916	snp	A/T	0.00795532	0.062565	intron-variant	MED16	GRCh38.p7	19:876138	TGCCGTGAATGGGAT[A/T]TTTTTTTTCCCATTT	10025
rs115652984	snp	C/T	0.00279162	0.0372561	intron-variant	MED16	GRCh38.p7	19:871723	GGGCTTATGTTCTGG[C/T]GGGGGGCTCAGGCAG	10025
rs115986208	snp	A/G	0.0263992	0.111815	intron-variant	MED16	GRCh38.p7	19:869368	CGGCCTGGAGGTGCC[A/G]GGACCTCTGAACGAC	10025
rs116042989	snp	A/G	0.0310518	0.120672	intron-variant	MED16	GRCh38.p7	19:884197	CATCTCCCTTCTCCA[A/G]AGCGGAGGCCAGCCT	10025
rs116095461	snp	A/G	0.00795532	0.062565	upstream-variant-2KB	MED16	GRCh38.p7	19:894407	AACTCCAGGCCTCAA[A/G]CCCTCCTTCCACCCC	10025
rs116283294	snp	A/G	0.182706	0.240773	intron-variant	MED16	GRCh38.p7	19:878432	ATGTCCACCAGCCCC[A/G]GCCCCGGCCCCGGCC	10025
rs116313463	snp	C/T	0.00358779	0.0422022	intron-variant	MED16	GRCh38.p7	19:872345	CAGAGTCGTCCCATC[C/T]CTGAGAGTCCACAAG	10025
rs116479143	snp	C/T	0.0178098	0.0926698	downstream-variant-500B	MED16	GRCh38.p7	19:867955	CACCGACGGCAGGGA[C/T]GCGGGCCTGGGCGCA	10025
rs116483371	snp	A/G	0.00755907	0.0610114	intron-variant	MED16	GRCh38.p7	19:870739	GAGCCGTATGGATTC[A/G]GGGGGGTCCTGGGGC	10025
rs116501596	snp	A/G	0.0260105	0.111035	intron-variant	MED16	GRCh38.p7	19:880630	TCCCTGCAGTAGAGA[A/G]GCTGCAAAGCCGGGC	10025
rs116591089	snp	A/G	0.00478085	0.0486577	intron-variant	MED16	GRCh38.p7	19:884432	GTGGGGTGGGGTGGG[A/G]GGCGTGTTCTCAGCA	10025
rs116674441	snp	A/G	0.00239004	0.0344864	synonymous-codon	MED16	GRCh38.p7	19:885908	CTTCTCGCTCACCAC[A/G]CTCACGCACACCTTG	10025
rs116702433	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:893417	AGGTCATTTAAGAGA[A/G]GTCGGCCTATGTGTA	10025
rs116716294	snp	C/T	0.00914312	0.0669923	intron-variant	MED16	GRCh38.p7	19:874735	ATTAAAAACCGGGTG[C/T]GGTGGCACGTGTCTG	10025
rs116793099	snp	G/T	0.0267878	0.112589	intron-variant	MED16	GRCh38.p7	19:870199	GCCTGACATCCAGGG[G/T]GGCCAGAGACTAAGG	10025
rs116797995	snp	A/G	0.0252325	0.109451	intron-variant	MED16	GRCh38.p7	19:880562	TTGTACGAGGGCCGG[A/G]GGGAGGTGGGGTCCA	10025
rs117089291	snp	C/G	0.00239393	0.0345281	intron-variant	MED16	GRCh38.p7	19:882564	CCAGAGAGCACGTGT[C/G]GGGGGTCCTGCTGTG	10025
rs117089972	snp	A/G	0.000317298	0.0125916	intron-variant	MED16	GRCh38.p7	19:881762	AATGGAGTAAAGACA[A/G]GCTGAGACAGCCGCA	10025
rs117097731	snp	A/C/G	0.0198897	0.0977218	synonymous-codon	MED16	GRCh38.p7	19:880081	GGAGCTGTAGAAGAC[A/C/G]GCCATGGTCTGCAGT	10025
rs117112597	snp	A/G	0.00835141	0.0640778	intron-variant	MED16	GRCh38.p7	19:886564	TGGCTCTGCCGTGGC[A/G]GCACACAGGCAGCTG	10025
rs117182092	snp	C/T	0.00159617	0.0282053	intron-variant	MED16	GRCh38.p7	19:874404	CACGAGTCGCCACGC[C/T]CAGCAACCCTAATTT	10025
rs117191854	snp	A/C/G	0.0001154	0.00759533	missense	MED16	GRCh38.p7	19:880058	TCATCCACAGGCCTC[A/C/G]GGGCCGCGGAGCTGT	10025
rs117226930	snp	C/G	0.00636936	0.0560724	intron-variant	MED16	GRCh38.p7	19:869287	GAAGGTGCTTGTGAC[C/G]CTCCCATTTGAGGCT	10025
rs117346489	snp	C/T	0.00716266	0.059414	utr-variant-3-prime	MED16	GRCh38.p7	19:867988	GGGCGTTTATTGGAC[C/T]TGTCCTTCCCAGCCG	10025
rs117376574	snp	G/T	0.0618563	0.164627	intron-variant	MED16	GRCh38.p7	19:882907	TGAGCAGCATTCCCT[G/T]GGGGGAAACAGGCCC	10025
rs117381356	snp	C/T	0.0498117	0.149749	intron-variant	MED16	GRCh38.p7	19:888773	GTGCTGCGTGTACTG[C/T]GGCAATGCGCCGACA	10025
rs117463628	snp	A/G	0.0437281	0.141251	intron-variant	MED16	GRCh38.p7	19:874397	GATTACACACGAGTC[A/G]CCACGCCCAGCAACC	10025
rs117481646	snp	C/G	0.0123036	0.0774623	intron-variant	MED16	GRCh38.p7	19:869113	GGTGCGGGACCACCT[C/G]AGACAGGCCCAGTAA	10025
rs117552999	snp	C/T	0.0178098	0.0926698	intron-variant	MED16	GRCh38.p7	19:881326	CAATGACTCTTTACA[C/T]ATTAAAGAACACTGG	10025
rs117592485	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:874929	GCACTTTAGGAGGCC[A/G]AGGCGGGCGGATCAT	10025
rs117636494	snp	C/T	0.0441095	0.141807	intron-variant	MED16	GRCh38.p7	19:888630	GTGGGCTGCACACTC[C/T]CAATGGGTGAGTTCT	10025
rs117764461	snp	A/G	0.0448719	0.142907	intron-variant	MED16	GRCh38.p7	19:882778	GCTTGTTACTCGGCT[A/G]AAGCTGACTACCACG	10025
rs117801197	snp	C/T	0.081446	0.184634	utr-variant-3-prime	MED16	GRCh38.p7	19:868002	CCTGTCCTTCCCAGC[C/T]GCTGCTTGTCCAGGT	10025
rs117962128	snp	C/T	0.00197525	0.0313644	synonymous-codon	MED16	GRCh38.p7	19:884994	GCTGGTCTGGCTGGA[C/T]GCGCACAAAAGCACC	10025
rs118130273	snp	C/T	0.0111196	0.0737302	intron-variant	MED16	GRCh38.p7	19:886386	CCTCCGTCTCCTCAT[C/T]TGTAAGGTGGAAGGA	10025
rs137907304	snp	A/G	0.0130921	0.0798413	intron-variant	MED16	GRCh38.p7	19:869635	GAGCCAAGCCAGGGC[A/G]CCTTCCCGGAGGTCC	10025
rs137921458	snp	A/G			intron-variant	MED16	GRCh38.p7	19:871786	GAGAGGGGAGAGGGG[A/G]GAGCGGGGAGAAGGG	10025
rs137926861	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:884588	CTCCACAGCCGCCCA[C/T]ACGCCTGCAGCCCCT	10025
rs137959900	snp	A/C/G	9.65641e-05	0.00694794	missense	MED16	GRCh38.p7	19:868153	CTGGGGGTCCTGGGA[A/C/G]AGTGGTGTGTGGACT	10025
rs137976345	snp	A/G			intron-variant	MED16	GRCh38.p7	19:878687	TGCCCAACAGCCCCA[A/G]CCCCACGTGCCCCAG	10025
rs137978287	snp	A/C	0.000153988	0.00877327	missense	MED16	GRCh38.p7	19:885978	GCCACCACGATGTTG[A/C]CGCCGCCGGTGAAGG	10025
rs138025525	snp	A/C/G	0.00880818	0.0657762	intron-variant	MED16	GRCh38.p7	19:890337	GGTAAGCCGGTGTGT[A/C/G]TCCCACCCCAGGAAG	10025
rs138044206	snp	C/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:882257	TCACATCTGCCACCC[C/G]AAGACTTTGGGAAGC	10025
rs138187794	snp	C/T	3.33717e-05	0.0040847	missense	MED16	GRCh38.p7	19:873534	TGCAGTGTGTTCATG[C/T]CCAGCACAAATTCCT	10025
rs138267754	snp	A/G	0.0023933	0.0345097	intron-variant	MED16	GRCh38.p7	19:890638	GGGCACAGCCACCAC[A/G]CACCTTTCAAAAACC	10025
rs138320149	snp	A/G	0.00162904	0.0284933	synonymous-codon	MED16	GRCh38.p7	19:885842	CTTGCGGTTGAGGTC[A/G]GTGGTGCAGCGCATG	10025
rs138329629	snp	A/G	0.000103345	0.00718761	synonymous-codon	MED16	GRCh38.p7	19:875416	GGGCGACAGCTTGCA[A/G]AGCGAGGCCTTCATG	10025
rs138392000	snp	A/G	0.00358779	0.0422022	downstream-variant-500B	MED16	GRCh38.p7	19:867698	AAACAAGGAGAGCAC[A/G]CAGAGACAGTATAGA	10025
rs138656682	snp	A/T	0.0429648	0.14013	intron-variant	MED16	GRCh38.p7	19:887448	CGAGGCGGGCAGATC[A/T]CAAGGTCAGGAGTTC	10025
rs138736652	snp	C/G/T	0.000312861	0.0125035	synonymous-codon, intron-variant	MED16	GRCh38.p7	19:876998	GGCAGCGGTCTGGCG[C/G/T]GTGTACTCCTCGTGC	10025
rs138793388	snp	C/T	2.32129e-05	0.00340674	missense	MED16	GRCh38.p7	19:868184	GCGGGCCCAGCTGGA[C/T]AAAGGCAGGGGCTTC	10025
rs138860392	snp	A/G	0.00810076	0.063125	intron-variant	MED16	GRCh38.p7	19:873412	TGAGATGGGGGCCCA[A/G]GTGGGGGGCGGGGCC	10025
rs138972499	snp	A/G	0.0142736	0.0832652	intron-variant	MED16	GRCh38.p7	19:876229	CCACGTGCAGCTGCC[A/G]GCTGAGCTCGTTAGA	10025
rs139020974	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, nc-transcript-variant	MED16, RNU6-9	GRCh38.p7	19:893484	TGGAACTCAATATTC[A/G]TGCTCGCTTCGGCAG	10025
rs139047798	snp	A/G	4.15041e-05	0.00455525	missense, intron-variant	MED16	GRCh38.p7	19:877155	AGCGGGTGGCCCATG[A/G]AAGGTGAGAGGCGGA	10025
rs139216027	snp	A/G	8.37556e-05	0.00647076	synonymous-codon	MED16	GRCh38.p7	19:885914	GCTCACCACGCTCAC[A/G]CACACCTTGTAGAAC	10025
rs139270233	snp	A/G	0.00279162	0.0372561	intron-variant	MED16	GRCh38.p7	19:887941	GGCACAGTGACTCAC[A/G]CCTGTCATCCCAGCA	10025
rs139276462	snp	A/G	0.000140085	0.00836798	synonymous-codon	MED16	GRCh38.p7	19:880120	GTGCACGATGTGGAC[A/G]CTGCCGTCGTGGAAG	10025
rs139294457	snp	A/G	9.75467e-05	0.00698311	synonymous-codon, utr-variant-5-prime	MED16	GRCh38.p7	19:890204	CGAGTGCAGGTCCCA[A/G]GGGTGCTCCGTGTCC	10025
rs139394580	snp	C/T	0.0768938	0.180373	intron-variant	MED16	GRCh38.p7	19:886232	GGAGGGAGGAGGGGC[C/T]GCTCAGGCTCATGGG	10025
rs139472527	snp	A/G	0.0310518	0.120672	intron-variant	MED16	GRCh38.p7	19:870709	ATGGCCATGACTGGA[A/G]AACATGGAGGGAAGG	10025
rs139539918	snp	A/G	0.00279162	0.0372561	intron-variant	MED16	GRCh38.p7	19:873978	CTGGCAGCTGGCGGC[A/G]GTTACACACCCAACA	10025
rs139550369	snp	A/G	6.75208e-05	0.00580998	missense	MED16	GRCh38.p7	19:868480	TGTTGGGCGACTTGA[A/G]CATGGTGACACAGCC	10025
rs139560649	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:892061	GGAACACCTGTGGCC[A/G]AGGCGGGGGCTGAGT	10025
rs139834365	snp	A/G	0.000728664	0.0190736	synonymous-codon	MED16	GRCh38.p7	19:868925	CCTCCGCAGGTGGTC[A/G]ATCTTGGGCTGGCCT	10025
rs139971279	snp	A/G	3.33923e-05	0.00408596	synonymous-codon	MED16	GRCh38.p7	19:881650	CGCCACGGCCGACAC[A/G]CGGTCCAGATCGTTG	10025
rs140017223	snp	A/G	0.0103295	0.0711199	intron-variant	MED16	GRCh38.p7	19:888244	GATAAAGGTCTGGCC[A/G]GGCTCGTTGGCTCAC	10025
rs140020652	snp	C/T	0.00874735	0.0655527	intron-variant	MED16	GRCh38.p7	19:879025	CCCCAGCCCCACATG[C/T]CCCAGCAGCTCACCT	10025
rs140168220	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:890896	TCAAGGCAGTGGGCC[A/G]GGCACCTGGGGAACA	10025
rs140253462	snp	C/T	8.33465e-05	0.00645495	synonymous-codon	MED16	GRCh38.p7	19:875326	AAAGTGGGGGCGCAG[C/T]AGCGACTTCAGGGTG	10025
rs140377139	snp	A/G	0.0103295	0.0711199	intron-variant	MED16	GRCh38.p7	19:883078	GCTAGTGGCCAGGGT[A/G]CCCTCACAGCACGAT	10025
rs140386082	snp	A/G	0.00199481	0.0315187	intron-variant	MED16	GRCh38.p7	19:869157	CCCCACACGGAGGAG[A/G]GTTGGTCTCCCAGGT	10025
rs140395847	snp	A/G	6.96512e-05	0.00590091	synonymous-codon, intron-variant	MED16	GRCh38.p7	19:877105	TGCAGTACTCCAGCA[A/G]GAAGAGCAGGTGCCG	10025
rs140413604	snp	A/G	1.69559e-05	0.00291164	missense	MED16	GRCh38.p7	19:872075	AGCATGCCCAGCGAG[A/G]TGCCGTCCCGCAGAA	10025
rs140480631	snp	C/T	0.00993419	0.0697739	intron-variant	MED16	GRCh38.p7	19:889265	GGCTCTGGGATGTTA[C/T]TAAATCAGAGGGTGG	10025
rs140500987	snp	C/T	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:882047	ACCCTAACACTCGCT[C/T]GGCCTTAGCCAGCTC	10025
rs140635640	snp	A/G	0.000649284	0.0180061	intron-variant	MED16	GRCh38.p7	19:868523	AGGCAGGCACTGAGC[A/G]GGTTCCCACTTCCAG	10025
rs140861688	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:887348	ATGTTAAAGGAGCAC[A/G]TGTGCCTTTTATTAA	10025
rs140879962	snp	C/T	0.00398564	0.0444627	intron-variant	MED16	GRCh38.p7	19:885689	CCGTGGAGGCCCGCG[C/T]GGGTCTCCACCCCCA	10025
rs140967546	snp	A/G	1.97693e-05	0.00314392	synonymous-codon	MED16	GRCh38.p7	19:880000	CTGCATAGCCTTTAA[A/G]TGGACGGCGGGGCCC	10025
rs140979236	snp	A/G	0.00159617	0.0282053	intron-variant	MED16	GRCh38.p7	19:871417	CCAGGTCGGGGCCCC[A/G]GCTCTGCCTGCCTGG	10025
rs141014120	in-del	-/GCCCCGGCCCCGGCCCCG			intron-variant	MED16	GRCh38.p7	19:878917	TGTCAATGTCCACCA[-/GCCCCGGCCCCGGCCCCG]GCCCCGGCCCCGGCC	10025
rs141074296	snp	A/C			intron-variant	MED16	GRCh38.p7	19:878678	GGTTGTCAATGCCCA[A/C]CAGCCCCAACCCCAC	10025
rs141098575	snp	A/G	0.00199481	0.0315187	intron-variant	MED16	GRCh38.p7	19:890050	TCTAGACCCAGCGCC[A/G]GACTCCAGACTGACC	10025
rs141198172	snp	A/G	0.00398564	0.0444627	intron-variant	MED16	GRCh38.p7	19:872847	TGGGGCTGAGAAGGA[A/G]CAGGGCCTGGGAGGC	10025
rs141292039	snp	C/T	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:883802	TGCTGCAGGAGCCAG[C/T]GCAGCCCAAACTGCC	10025
rs141295603	snp	C/T	0.0111196	0.0737302	intron-variant	MED16	GRCh38.p7	19:874743	CCGGGTGTGGTGGCA[C/T]GTGTCTGTAATCCCA	10025
rs141323279	snp	G/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:886437	GACAGTGGGGAGGAT[G/T]AAACGGGTGAACGTG	10025
rs141399595	snp	C/T	0.284471	0.247612	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:892998	CGACCCCGCAGGCCC[C/T]GCCACGGCTGCGCCG	10025
rs141522921	snp	C/T	1.69195e-05	0.00290851	synonymous-codon	MED16	GRCh38.p7	19:885938	GTAGAACTGCACGGG[C/T]GACGCGCTGCTGCCG	10025
rs141601240	snp	A/C/G	0.000524144	0.0161804	synonymous-codon	MED16	GRCh38.p7	19:875251	GGACCCACCGACGTC[A/C/G]GTGATCTTGGTGCAG	10025
rs141659212	snp	A/G	0.000340078	0.0130355	intron-variant	MED16	GRCh38.p7	19:890374	GAACTGCTGTCAGCC[A/G]AGTCGACAGCTCAGG	10025
rs141690525	snp	A/C	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:882949	GAGACGCCCAGAGGG[A/C]ACACAGTGGTCAGGG	10025
rs141789160	snp	A/G	0.000798403	0.0199641	downstream-variant-500B	MED16	GRCh38.p7	19:867486	CACTGTGCTGGGAAG[A/G]CCTGCTGGAGACGGA	10025
rs141845969	snp	A/G	0.00438332	0.0466095	intron-variant	MED16	GRCh38.p7	19:882551	CAAAAACAGTGGCCC[A/G]GAGAGCACGTGTGGG	10025
rs141860145	snp	A/G	0.0111196	0.0737302	intron-variant	MED16	GRCh38.p7	19:884156	CGCTAATCGGCAAAT[A/G]CCTGTGCTCTCATCT	10025
rs141930803	snp	A/G/T	0.00339085	0.0410368	synonymous-codon	MED16	GRCh38.p7	19:872002	GGTGGCCGTATACAC[A/G/T]GGCAGGCAGCTGGGC	10025
rs141936460	in-del	-/GT	0.00874735	0.0655527	intron-variant	MED16	GRCh38.p7	19:872643	CTGGGGCAGGACAGA[-/GT]GTACCGGCGGGGGGG	10025
rs141978012	snp	A/G	1.70374e-05	0.00291863	missense	MED16	GRCh38.p7	19:871991	TGGGTATCCGAGGTG[A/G]CCGTATACACGGGCA	10025
rs142169648	snp	A/G	0.0134861	0.0810011	intron-variant	MED16	GRCh38.p7	19:883969	GGAAGGAATGGCAGT[A/G]GCCCTCTTCACCTTT	10025
rs142199789	snp	A/C	0.00199481	0.0315187	upstream-variant-2KB, nc-transcript-variant	MED16, RNU6-9	GRCh38.p7	19:893500	TGCTCGCTTCGGCAG[A/C]ACATATACTAAAATT	10025
rs142254775	snp	A/G	3.90602e-05	0.00441912	missense	MED16	GRCh38.p7	19:868157	GGGTCCTGGGAGAGT[A/G]GTGTGTGGACTGCGG	10025
rs142344850	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:874496	CAGAGGCGAGTAGGA[C/T]ACCACGTGCTGGGTG	10025
rs142353451	snp	A/G	1.65963e-05	0.0028806	synonymous-codon, utr-variant-5-prime	MED16	GRCh38.p7	19:891003	GGTGAAGGCGATGAG[A/G]TTTCGGCAGGACCAG	10025
rs142466928	snp	A/G	0.000307508	0.012396	intron-variant	MED16	GRCh38.p7	19:885760	CACGTGATGGCCTGC[A/G]CCCGTTCACCTGCTC	10025
rs142515269	snp	A/G	0.00128677	0.0253324	synonymous-codon	MED16	GRCh38.p7	19:881602	GGCCACCTTGAGGTC[A/G]GTGTTGGTGAGCGAG	10025
rs142533778	snp	C/T	0.00914312	0.0669923	intron-variant	MED16	GRCh38.p7	19:882437	GAGGCTGAGGTAGGA[C/T]TGCTCGAGCCCAGGA	10025
rs142617617	snp	A/G			intron-variant	MED16	GRCh38.p7	19:877685	GTGCCCCAGCAGCTC[A/G]CCTTCCCCTGGTTGT	10025
rs142620365	snp	A/C/T	0.000183443	0.00957549	synonymous-codon	MED16	GRCh38.p7	19:885878	GGAGGGCAGGATCTC[A/C/T]GTGTCGATACGGCAC	10025
rs142622834	snp	A/C/G	0.000203236	0.0100787	synonymous-codon, intron-variant	MED16	GRCh38.p7	19:889686	GTGCAGCCAGGACAG[A/C/G]GCCACAATGGGGTCC	10025
rs142624165	snp	A/G	0.000187712	0.0096861	synonymous-codon	MED16	GRCh38.p7	19:881560	TGGCTCCACCGTACC[A/G]AGGCCAGGGTAGAAC	10025
rs142733090	snp	A/C/G/T	0.00226555	0.0335842	missense, synonymous-codon	MED16	GRCh38.p7	19:880126	GATGTGGACGCTGCC[A/C/G/T]TCGTGGAAGGCCAGG	10025
rs142750910	snp	A/C	0.00358779	0.0422022	intron-variant	MED16	GRCh38.p7	19:885463	CACGTTGGGGGGGGT[A/C]CGGGGGCCCCAGTGT	10025
rs142768500	snp	A/C/T	3.33501e-05	0.0040834	synonymous-codon	MED16	GRCh38.p7	19:873551	CAGCACAAATTCCTC[A/C/T]GTCTTGAGGTTGATC	10025
rs142854565	snp	A/C	0.361894	0.223562	intron-variant	MED16	GRCh38.p7	19:879295	GCAGCTCACCTTCCC[A/C]TGGTTGTCAATGCCC	10025
rs142896150	snp	C/T	0.000181113	0.00951441	synonymous-codon, intron-variant	MED16	GRCh38.p7	19:876980	GGCCCCCACCTGCTG[C/T]AGGGCAGCGGTCTGG	10025
rs142974827	snp	A/G	0.00517822	0.0506191	intron-variant	MED16	GRCh38.p7	19:888073	GCCGGGCGTGGTGGC[A/G]GGCGCCTGTAATCCC	10025
rs142981293	snp	C/G/T	0.00119737	0.0244387	upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:893462	AGGGGCTTTAAATAG[C/G/T]TGGTGGTGGAACTCA	10025
rs142982212	snp	A/G	0.0149017	0.0850223	intron-variant	MED16	GRCh38.p7	19:868276	GGGCTGAGGTTAACC[A/G]CGCCGAGGAGAGTCC	10025
rs143014203	snp	A/G	0.00169555	0.0290671	synonymous-codon	MED16	GRCh38.p7	19:872080	GCCCAGCGAGGTGCC[A/G]TCCCGCAGAAAGCTG	10025
rs143072094	snp	A/G	0.00199481	0.0315187	upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:893256	CTGCCCCGCCTCCGG[A/G]GCTATTTGCATACGA	10025
rs143154170	in-del	-/C	0.181181	0.240341	intron-variant	MED16	GRCh38.p7	19:876933	CCACCTGCCACAGGG[-/C]CCCCACCTGCCACGG	10025
rs143367239	snp	C/T	0.000117948	0.00767854	synonymous-codon	MED16	GRCh38.p7	19:880015	GTGGACGGCGGGGCC[C/T]GCGGTGCGGGGGCGC	10025
rs143373467	in-del	-/ACTC	0.0341408	0.126114	intron-variant	MED16	GRCh38.p7	19:889356	CCAGTGAAAGAGATA[-/ACTC]ACTAAGAACGGCCAC	10025
rs143476326	snp	A/G	0.00557542	0.0525036	intron-variant	MED16	GRCh38.p7	19:876193	CACAGAGGAAAACAA[A/G]TGAAGCTCAGAGGGC	10025
rs143512436	snp	C/T	0.000417324	0.0144391	missense	MED16	GRCh38.p7	19:881651	GCCACGGCCGACACA[C/T]GGTCCAGATCGTTGG	10025
rs143513224	in-del	-/C			intron-variant	MED16	GRCh38.p7	19:889051	CCTACTCTTAACTGT[-/C]CCCCCCCAACCCTGG	10025
rs143517669	snp	C/T	0.0490761	0.14876	utr-variant-3-prime	MED16	GRCh38.p7	19:868083	GGTCACCACAAGGTC[C/T]GCCTGGACCCCCGGC	10025
rs143531881	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:869697	GTCCTGGAGCCGAGC[C/T]GGGGCCTTCCCCGGA	10025
rs143625341	snp	A/G			intron-variant	MED16	GRCh38.p7	19:868340	CAGGGGCAGCTGAGG[A/G]GTAGCTGAGGAGTAG	10025
rs143653291	snp	A/G	8.31566e-05	0.00644759	synonymous-codon	MED16	GRCh38.p7	19:885839	GTCCTTGCGGTTGAG[A/G]TCGGTGGTGCAGCGC	10025
rs143687248	snp	C/T	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:886441	GTGGGGAGGATTAAA[C/T]GGGTGAACGTGTGCG	10025
rs143723258	snp	A/G	0.00438332	0.0466095	intron-variant	MED16	GRCh38.p7	19:883719	ATGGTAGACACAGAC[A/G]TGCCCAGCGGGGGCA	10025
rs143762645	snp	C/T	0.000545703	0.0165092	missense, utr-variant-5-prime	MED16	GRCh38.p7	19:891080	TCTCCCACTCACAGA[C/T]GTAGGCCAAGTCCAT	10025
rs143864614	snp	A/C	0.0170251	0.090679	intron-variant	MED16	GRCh38.p7	19:885396	CTGGGCCGCCTCTCA[A/C]AGAGAAGGGACCTGC	10025
rs143896429	snp	C/T	0.0162398	0.0886349	intron-variant	MED16	GRCh38.p7	19:870496	AACCCGAGAGGCAGA[C/T]GTTGCAGTGGGCCAA	10025
rs143998221	snp	A/G	0.000135837	0.00824016	synonymous-codon, intron-variant	MED16	GRCh38.p7	19:877052	CATACTGGGCTGCAC[A/G]TGCAGCAGGATGTCC	10025
rs144143613	snp	C/T	7.64862e-05	0.00618363	missense	MED16	GRCh38.p7	19:880080	CGGAGCTGTAGAAGA[C/T]GGCCATGGTCTGCAG	10025
rs144226399	snp	C/G	0.0111196	0.0737302	intron-variant	MED16	GRCh38.p7	19:874163	CTGTCGCCCAGGCTG[C/G]AGTGCAGTGGGGTGA	10025
rs144263769	snp	C/T	0.000429224	0.0146434	synonymous-codon	MED16	GRCh38.p7	19:868230	GGTCACGCAGGCGTC[C/T]GGCCCACGGCCTTCA	10025
rs144273899	snp	A/T	0.0379877	0.132479	upstream-variant-2KB, downstream-variant-500B	MED16, RNU6-9	GRCh38.p7	19:893819	CCAGGGTGGTCTCTA[A/T]CTACTGACCTCCTGA	10025
rs144312426	snp	A/G	0.0267878	0.112589	intron-variant	MED16	GRCh38.p7	19:870762	CCTGGGGCAGGACAT[A/G]GAGGGAGGGAGCCGT	10025
rs144329323	snp	C/G	0.00636936	0.0560724	intron-variant	MED16	GRCh38.p7	19:870196	GAGGCCTGACATCCA[C/G]GGGGGCCAGAGACTA	10025
rs144332170	snp	A/G	5.437e-05	0.00521364	missense, intron-variant	MED16	GRCh38.p7	19:877125	AGCAGGTGCCGCAGC[A/G]CCAGCCCCACCTCCA	10025
rs144353862	in-del	-/CC	0.064146	0.167207	intron-variant	MED16	GRCh38.p7	19:881836	CCAGGTCTCATGCCG[-/CC]CTGCTCCCATGCCCA	10025
rs144442835	snp	C/T	0.00953873	0.0683987	intron-variant	MED16	GRCh38.p7	19:882693	TGGGAACCAGGAGAG[C/T]GCAGCTGAGGCAGCC	10025
rs144451134	snp	A/G			intron-variant	MED16	GRCh38.p7	19:878178	TTGTCAATGCCCACC[A/G]AGCCCAGCCCCACGT	10025
rs144469187	snp	G/T	0.00252525	0.0354436	synonymous-codon	MED16	GRCh38.p7	19:868865	GGGGGCCCCTCACCT[G/T]GTGCAGGCCTTGCAT	10025
rs144506957	snp	A/C/G	0.000411764	0.0143429	missense, synonymous-codon	MED16	GRCh38.p7	19:880129	GTGGACGCTGCCGTC[A/C/G]TGGAAGGCCAGGGCC	10025
rs144537136	snp	A/G	0.000307991	0.0124057	utr-variant-3-prime	MED16	GRCh38.p7	19:868100	CCTGGACCCCCGGCC[A/G]TCACGGACGGTCCTC	10025
rs144757347	snp	C/T			intron-variant	MED16	GRCh38.p7	19:882442	TGAGGTAGGATTGCT[C/T]GAGCCCAGGAAGATG	10025
rs144849703	snp	A/G/T	0.000873789	0.0208837	missense, synonymous-codon, intron-variant	MED16	GRCh38.p7	19:877010	GCGCGTGTACTCCTC[A/G/T]TGCAGCTTCTCCACC	10025
rs144892801	snp	C/T	0.00119737	0.0244387	utr-variant-5-prime, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:893154	GCGCCTCGGGTCTGG[C/T]GCCGCCATCTTCCTC	10025
rs144975900	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:889574	GAGAGGAGAGGGGCT[A/G]GCGGGTGGCTGGGTA	10025
rs145005716	snp	A/C/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:868595	GGTCTCCCTCTGCTC[A/C/G]CCGTCCCTCACGCCT	10025
rs145091342	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:893475	AGCTGGTGGTGGAAC[C/T]CAATATTCGTGCTCG	10025
rs145093835	snp	C/T	8.08653e-05	0.00635815	synonymous-codon	MED16	GRCh38.p7	19:879982	CAGTGACGTCCACGA[C/T]AGCTGCATAGCCTTT	10025
rs145097180	snp	A/G	0.000153988	0.00877328	missense	MED16	GRCh38.p7	19:875318	GTGTTGAGAAAGTGG[A/G]GGCGCAGCAGCGACT	10025
rs145164398	snp	A/C/G	0.000160688	0.00896216	missense, synonymous-codon	MED16	GRCh38.p7	19:871962	GCAGGCGGAAGAGCA[A/C/G]GGACATGCTGTCCTG	10025
rs145239515	in-del	-/A	0.0460142	0.144533	intron-variant	MED16	GRCh38.p7	19:887186	TCTAAGTTACAAGTT[-/A]AAAAAAAAACACTTC	10025
rs145251549	snp	C/G			intron-variant	MED16	GRCh38.p7	19:879380	CCACCAGCCCCAGCC[C/G]CACATGCCCCAGCAG	10025
rs145458567	snp	A/G	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:876009	GCGACGGCCCAAGGA[A/G]GGAGAGGGCGAGGTC	10025
rs145483089	snp	A/G	0.000266742	0.0115456	synonymous-codon	MED16	GRCh38.p7	19:875350	CAGGGTGGAGCTGAT[A/G]GCGATGAGGAAGAGC	10025
rs145561063	snp	A/G	0.000248749	0.0111496	intron-variant	MED16	GRCh38.p7	19:871691	AGATATCAAGGCAGA[A/G]CCACTGCCACCTGCA	10025
rs145685485	snp	C/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:880519	TAGGGTGGTGGGCTG[C/G]GGCTGTCACTCACAC	10025
rs145707212	snp	A/C/G	0.000302123	0.0122875	synonymous-codon	MED16	GRCh38.p7	19:873488	GTACAGCACGAAGTC[A/C/G]CCCACCCACTGCAAG	10025
rs145715055	snp	G/T	0.00318978	0.0398085	intron-variant	MED16	GRCh38.p7	19:883540	GTGGGGACTGTCCCA[G/T]TGACCCCCAGCTGCC	10025
rs145774765	snp	A/G	0.00636936	0.0560724	intron-variant	MED16	GRCh38.p7	19:876613	CCTGGACGGGCCTCT[A/G]GGAGCACACCCCACA	10025
rs145956215	in-del	-/GCCCCAGCCCCACGT			intron-variant	MED16	GRCh38.p7	19:879675	TGTCAATGCCCACCA[-/GCCCCAGCCCCACGT]GCCCCAGCAGCTCGC	10025
rs146130229	snp	A/C	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:889959	CGCACTCCAGAGATG[A/C]CCTGAGACACCCTGA	10025
rs146141347	snp	A/G	0.00020006	0.0099995	synonymous-codon	MED16	GRCh38.p7	19:873560	TTCCTCCGTCTTGAG[A/G]TTGATCATGACCTTG	10025
rs146159593	snp	A/G	0.000274964	0.0117221	synonymous-codon	MED16	GRCh38.p7	19:868898	CTCCGTGGGGCAAGC[A/G]CCAAGGTGCAGCCTC	10025
rs146234209	snp	A/G/T	0.000108262	0.00735669	synonymous-codon	MED16	GRCh38.p7	19:868173	GTGTGTGGACTGCGG[A/G/T]CCCAGCTGGACAAAG	10025
rs146290617	snp	A/G	0.0134861	0.0810011	intron-variant	MED16	GRCh38.p7	19:891384	GAGCCCGGGAGGGCT[A/G]GGACCTATTTGGGTT	10025
rs146295365	snp	A/G	0.000430585	0.0146665	synonymous-codon	MED16	GRCh38.p7	19:868427	GCACAGGCAGTTCTT[A/G]ATCCAGCGCTGCTCC	10025
rs146302316	snp	A/G	0.0217236	0.101931	intron-variant	MED16	GRCh38.p7	19:870512	GTTGCAGTGGGCCAA[A/G]ACGGCACTACTGCAC	10025
rs146316247	snp	A/G	0.00438332	0.0466095	upstream-variant-2KB, nc-transcript-variant	MED16, RNU6-9	GRCh38.p7	19:893503	TCGCTTCGGCAGCAC[A/G]TATACTAAAATTGGA	10025
rs146383901	snp	C/G	0.0178616	0.0932142	intron-variant	MED16	GRCh38.p7	19:873776	CACTGCCTGCCCCCC[C/G]CCGGGGGCCGCTGTG	10025
rs146447195	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:881867	AGAAGACCAGGCCCG[A/G]CCAATCCGAGCGCTT	10025
rs146459484	in-del	-/C	0.0456336	0.143994	intron-variant	MED16	GRCh38.p7	19:872613	GCCGGGTGGGTGGGG[-/C]AGAAGAAATCACAGC	10025
rs146584285	in-del	-/CCAGCC			intron-variant	MED16	GRCh38.p7	19:879062	GGTTGTCAATGCCCA[-/CCAGCC]CCAGCCCCAGCCCCA	10025
rs146602511	snp	A/C/G	0.00996614	0.0698848	missense	MED16	GRCh38.p7	19:868105	ACCCCCGGCCGTCAC[A/C/G]GACGGTCCTCTGGAT	10025
rs146712464	snp	C/G			intron-variant	MED16	GRCh38.p7	19:878283	GCAGCTCGCCTTCCC[C/G]TGGTTGTCAATGCCC	10025
rs146721272	snp	A/G	0.000809553	0.0201028	synonymous-codon	MED16	GRCh38.p7	19:884907	GGGAGACTCACCCAC[A/G]GGGGAGATCTGCTGG	10025
rs146736796	snp	C/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:886456	CGGGTGAACGTGTGC[C/G]CAACGGGAGTCACCT	10025
rs146740386	snp	A/G	0.000215031	0.0103667	missense	MED16	GRCh38.p7	19:880023	CGGGGCCCGCGGTGC[A/G]GGGGCGCTTCATGGC	10025
rs146823516	snp	A/T	0.0185938	0.0946107	intron-variant	MED16	GRCh38.p7	19:888403	GTGGTGGGTGCCTGT[A/T]ATCCCAGCTACTCAG	10025
rs146876080	snp	A/G			stop-gained, utr-variant-5-prime	MED16	GRCh38.p7	19:891008	AGGCGATGAGATTTC[A/G]GCAGGACCAGGCGCA	10025
rs146923019	snp	C/G	0.0103295	0.0711199	intron-variant	MED16	GRCh38.p7	19:890056	CCCAGCGCCGGACTC[C/G]AGACTGACCGGAGAA	10025
rs146928647	snp	A/G	0.000220726	0.0105031	missense	MED16	GRCh38.p7	19:868127	CCTCTGGATGCAGAT[A/G]GTCCAGGGATCTGGG	10025
rs146932760	snp	A/G	0.0138799	0.0821421	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:893015	CCACGGCTGCGCCGC[A/G]TTCCCTCGGGTCCGT	10025
rs146942398	snp	C/T	0.00398564	0.0444627	intron-variant	MED16	GRCh38.p7	19:869506	TTTACAAGCCTCTGA[C/T]GTAACCGTCCTCTCT	10025
rs146998459	snp	A/C/T	0.0852314	0.191298	intron-variant	MED16	GRCh38.p7	19:871767	GTAGGGAGAGGGGAG[A/C/T]GGGGAGAGGGGAGAG	10025
rs147055199	in-del	-/C			intron-variant	MED16	GRCh38.p7	19:876880	CCACCTGCCACGGGG[-/C]CCCCACCTGCCACGG	10025
rs147156588	snp	A/G	0.00676609	0.0577691	intron-variant	MED16	GRCh38.p7	19:870010	GGGCAGCCAGGGTCA[A/G]CTCAGCACACTTGGG	10025
rs147300279	snp	C/G	0.00358779	0.0422022	intron-variant	MED16	GRCh38.p7	19:885473	GGGGTCCGGGGGCCC[C/G]AGTGTCCTCACAGGG	10025
rs147347173	snp	A/G	0.00636936	0.0560724	downstream-variant-500B	MED16	GRCh38.p7	19:867791	CCCATCCCATCCACC[A/G]GCCTGCTGTGTCCTG	10025
rs147510499	snp	C/G	0.0177959	0.092639	missense	MED16	GRCh38.p7	19:868108	CCCGGCCGTCACGGA[C/G]GGTCCTCTGGATGCA	10025
rs147594897	snp	A/G	0.000153988	0.00877328	synonymous-codon	MED16	GRCh38.p7	19:875325	GAAAGTGGGGGCGCA[A/G]CAGCGACTTCAGGGT	10025
rs147657855	snp	A/G	0.000149481	0.00864395	synonymous-codon, utr-variant-5-prime	MED16	GRCh38.p7	19:890997	GTCCATGGTGAAGGC[A/G]ATGAGATTTCGGCAG	10025
rs147752650	snp	A/C/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:881368	AGCCTCACAGATCCC[A/C/G]AAAGATGAGATCTGC	10025
rs147855474	snp	C/T	0.0577344	0.159793	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:892963	GCCTACCCAGCAGCC[C/T]TTGCTCCCGGCCACG	10025
rs147959035	snp	C/T	0.000115974	0.00761403	missense, utr-variant-5-prime	MED16	GRCh38.p7	19:891020	TTCGGCAGGACCAGG[C/T]GCAGGCCAGGGGCAC	10025
rs148064606	snp	C/T	0.0111196	0.0737302	intron-variant	MED16	GRCh38.p7	19:887297	GGTGTCCACACCACA[C/T]GTCTGTGTGGGTCGC	10025
rs148143550	in-del	-/G	0.0494327	0.149241	intron-variant	MED16	GRCh38.p7	19:870093	TGACCTCTTGCCCCC[-/G]GGAGATCCTCCTGAT	10025
rs148148157	snp	C/T	0.00597247	0.0543191	upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:893400	ATAGAGGTTAAATCT[C/T]TAGGTCATTTAAGAG	10025
rs148216322	snp	A/G			intron-variant	MED16	GRCh38.p7	19:879511	GTGCCCCAGCAGCTC[A/G]CCTTTCCCTGGTTGT	10025
rs148228984	snp	C/G	0.0158469	0.0875917	intron-variant	MED16	GRCh38.p7	19:872554	GACTTCAAACCGTCC[C/G]TGATGGGCGCGGTGG	10025
rs148290750	snp	C/T	1.91452e-05	0.0030939	missense	MED16	GRCh38.p7	19:880065	CAGGCCTCGGGGCCG[C/T]GGAGCTGTAGAAGAC	10025
rs148391834	snp	A/G	0.00993419	0.0697739	intron-variant	MED16	GRCh38.p7	19:882793	GAAGCTGACTACCAC[A/G]CAGCTGCTCTGTGCC	10025
rs148428449	snp	A/G	0.000354124	0.0133018	missense	MED16	GRCh38.p7	19:871953	GCTTGGTGAGCAGGC[A/G]GAAGAGCAGGGACAT	10025
rs148550951	snp	C/G	0.0460506	0.144768	intron-variant	MED16	GRCh38.p7	19:880406	CCCAGCTGGGCCCAT[C/G]TCCTGGCTGACACGC	10025
rs148553311	snp	A/G	0.000476029	0.0154204	synonymous-codon, intron-variant	MED16	GRCh38.p7	19:877028	CAGCTTCTCCACCAG[A/G]CTCTGTACCATACTG	10025
rs148587330	snp	A/G	0.0232847	0.105357	intron-variant	MED16	GRCh38.p7	19:888061	TACAAAAAAGCAGCC[A/G]GGCGTGGTGGCGGGC	10025
rs148735712	snp	G/T	0.0170251	0.090679	upstream-variant-2KB, downstream-variant-500B	MED16, RNU6-9	GRCh38.p7	19:893931	CAAGAGTGGGGAAAC[G/T]GTAAGCGAAGTCACC	10025
rs148851351	snp	C/G	0.00478085	0.0486577	intron-variant	MED16	GRCh38.p7	19:876083	CTGGGGTTTAGCCTC[C/G]CAGCCCCCGCCTGGG	10025
rs148896515	snp	A/C/G	0.000233514	0.010803	missense	MED16	GRCh38.p7	19:875364	TGGCGATGAGGAAGA[A/C/G]CTTGGTGTGGTAGTC	10025
rs148918948	snp	A/G	9.97738e-05	0.00706236	missense	MED16	GRCh38.p7	19:885832	GAAACTTGTCCTTGC[A/G]GTTGAGGTCGGTGGT	10025
rs148920686	snp	A/T	0.0146672	0.084371	intron-variant	MED16	GRCh38.p7	19:883580	AGACCTGAGAAAGGC[A/T]GTGGCATGTGTGTGA	10025
rs149070813	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:893252	GGCTCTGCCCCGCCT[C/G]CGGGGCTATTTGCAT	10025
rs149077051	snp	G/T	0.00446936	0.0470607	intron-variant	MED16	GRCh38.p7	19:868847	CTGGGAGTCAGCGGT[G/T]CCGGGGGCCCCTCAC	10025
rs149124128	snp	A/C/G	0.000140638	0.00838456	intron-variant	MED16	GRCh38.p7	19:889623	CTCATCCGCTCACTC[A/C/G]GGCAGGACACTCACC	10025
rs149237832	snp	A/G	0.00358779	0.0422022	downstream-variant-500B	MED16	GRCh38.p7	19:867703	AGGAGAGCACGCAGA[A/G]ACAGTATAGAGACAG	10025
rs149297998	snp	C/T	2.97739e-05	0.00385824	missense	MED16	GRCh38.p7	19:868226	TGCTGGTCACGCAGG[C/T]GTCCGGCCCACGGCC	10025
rs149302926	in-del	-/AGGG	0.000863732	0.0207634	intron-variant	MED16	GRCh38.p7	19:886211	GCCCGACTGTGGAGA[-/AGGG]AGGGAGGGAGGAGGG	10025
rs149343879	snp	C/G			intron-variant	MED16	GRCh38.p7	19:873131	GGCTCCGAGATGGGG[C/G]AGGGCTCCGAGGTGG	10025
rs149372848	snp	A/G	3.36905e-05	0.00410416	missense	MED16	GRCh38.p7	19:873471	GGTAGGCTGGCCAGC[A/G]GGTACAGCACGAAGT	10025
rs149409159	snp	C/G	0.00953873	0.0683987	intron-variant	MED16	GRCh38.p7	19:888001	TGAGGTTAGGAGTTC[C/G]AGACCACCCTGACCA	10025
rs149465001	snp	A/C/G	0.00149137	0.0272678	intron-variant	MED16	GRCh38.p7	19:884896	CCGCAGCCGGCGGGA[A/C/G]ACTCACCCACGGGGG	10025
rs149597265	snp	A/G	0.0329836	0.124112	upstream-variant-2KB, downstream-variant-500B	MED16, RNU6-9	GRCh38.p7	19:893797	AGACGGGGTTTCGCC[A/G]TGTTGGCCAGGGTGG	10025
rs149621419	snp	C/T	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:870149	GGCCATATGCTAAGG[C/T]GTCTCTCTCCATCCA	10025
rs149649968	snp	A/G/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:890688	AAAACTGGGGCACGT[A/G/T]TCTCCAACAAGCCTC	10025
rs149728749	snp	A/G	0.000693514	0.0186085	intron-variant	MED16	GRCh38.p7	19:871612	AACAGGTGCCTGGAA[A/G]TGGCTGCCATCCCAA	10025
rs149766887	in-del	-/C			intron-variant	MED16	GRCh38.p7	19:876711	CGCAGGGAAACCCCT[-/C]CCAGCTGCCACAACC	10025
rs149791734	snp	A/G	1.66818e-05	0.00288802	missense	MED16	GRCh38.p7	19:885807	AGGAACTTGAGGTGG[A/G]TGATGGCGGGAAACT	10025
rs149892081	snp	C/T	0.00793539	0.0624878	synonymous-codon	MED16	GRCh38.p7	19:880057	CTCATCCACAGGCCT[C/T]GGGGCCGCGGAGCTG	10025
rs149933504	snp	A/C	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:889395	GTTAAATGAGGGGCC[A/C]CTGAACACGCAGGTG	10025
rs149949825	snp	A/G	0.000436877	0.0147732	missense	MED16	GRCh38.p7	19:879945	AGCTCACCTTCCCGT[A/G]GCTGTCAATCCCCAC	10025
rs149986642	snp	C/T	0.00358779	0.0422022	intron-variant	MED16	GRCh38.p7	19:886288	CGCGCACAGAAGAAC[C/T]ACGCAGAAGCCAGGA	10025
rs150013868	in-del	-/G	0.0456336	0.143994	intron-variant	MED16	GRCh38.p7	19:887097	AAACAAAAAAAAAAA[-/G]AACAAGAAAAATGTC	10025
rs150017885	snp	A/G	0.000311951	0.0124851	missense, utr-variant-5-prime	MED16	GRCh38.p7	19:890236	GGATGTGGATCATGC[A/G]GGTCAGGTCTGTGGG	10025
rs150098458	snp	C/T	0.00557542	0.0525036	intron-variant	MED16	GRCh38.p7	19:875559	CACCAGGCGCTCGGT[C/T]AGCTGGGCAAGCTGC	10025
rs150156322	snp	C/T	0.0193772	0.0965046	downstream-variant-500B	MED16	GRCh38.p7	19:867505	GCTGGAGACGGAAGG[C/T]GGGACCCCTGGGGAC	10025
rs150192510	snp	A/G	0.000865854	0.0207889	synonymous-codon, intron-variant	MED16	GRCh38.p7	19:876989	CTGCTGCAGGGCAGC[A/G]GTCTGGCGCGTGTAC	10025
rs150418941	snp	C/G	0.00716266	0.059414	intron-variant	MED16	GRCh38.p7	19:882153	CCTGACAGCCCCTGC[C/G]TGAAGACGCAGCTCC	10025
rs150436099	snp	C/T			intron-variant	MED16	GRCh38.p7	19:878158	AGCAGCTCACCTTCC[C/T]GTGGTTGTCAATGCC	10025
rs150469412	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:890630	GAGAAGACGGGCACA[A/G]CCACCACGCACCTTT	10025
rs150470824	snp	A/G/T	3.81842e-05	0.00436931	synonymous-codon, missense	MED16	GRCh38.p7	19:880075	GGCCGCGGAGCTGTA[A/G/T]AAGACGGCCATGGTC	10025
rs150520747	snp	A/G	3.34035e-05	0.00408664	synonymous-codon	MED16	GRCh38.p7	19:881620	GTTGGTGAGCGAGAT[A/G]GGCAGCTTGGGCAGC	10025
rs150528593	snp	C/G	0.00478085	0.0486577	intron-variant	MED16	GRCh38.p7	19:882951	GACGCCCAGAGGGCA[C/G]ACAGTGGTCAGGGGT	10025
rs150627779	snp	C/G	0.00874735	0.0655527	intron-variant	MED16	GRCh38.p7	19:877370	TGCACAATGCCTCTG[C/G]GAACAGGGAAGGAAA	10025
rs150679084	snp	C/T	0.0178098	0.0926698	intron-variant	MED16	GRCh38.p7	19:873234	ACTCAGGAAGTGGGA[C/T]TCCAAGTAGGGGTGG	10025
rs150714727	snp	A/T	5.84641e-05	0.00540635	missense, intron-variant	MED16	GRCh38.p7	19:877146	CCCACCTCCAGCGGG[A/T]GGCCCATGGAAGGTG	10025
rs150802169	in-del	-/CCAGCCCCGGCC			intron-variant	MED16	GRCh38.p7	19:878914	GGTTGTCAATGTCCA[-/CCAGCCCCGGCC]CCGGCCCCGGCCCCG	10025
rs150872840	snp	A/G	3.34107e-05	0.00408708	synonymous-codon	MED16	GRCh38.p7	19:875287	GGTCAGCCGGTCGCC[A/G]GGGCTCTTGTCAGGC	10025
rs150897851	snp	A/G	2.02039e-05	0.00317829	synonymous-codon	MED16	GRCh38.p7	19:886040	CCGGCACAGGCTCTC[A/G]GTGGACGTCAGCACC	10025
rs150974778	snp	A/C/G	0.000100339	0.00708235	synonymous-codon	MED16	GRCh38.p7	19:875386	GTGGTAGTCGCACAC[A/C/G]CGGGTCACCGTGCAG	10025
rs151071484	snp	A/G	0.00318978	0.0398085	intron-variant	MED16	GRCh38.p7	19:883728	ACAGACGTGCCCAGC[A/G]GGGGCACCGGGCAGT	10025
rs151108401	snp	A/G	0.00953873	0.0683987	intron-variant	MED16	GRCh38.p7	19:868320	GCTCTTGCAGCAGCC[A/G]GGCTCAGGGGCAGCT	10025
rs151113242	in-del	-/C			intron-variant	MED16	GRCh38.p7	19:873769	GGAGCCCACTGCCTG[-/C]CCCCCCCCCGGGGGC	10025
rs151170454	snp	A/C/G	0.000520945	0.016131	missense	MED16	GRCh38.p7	19:868109	CCGGCCGTCACGGAC[A/C/G]GTCCTCTGGATGCAG	10025
rs151197059	snp	C/G	0.00795532	0.062565	intron-variant	MED16	GRCh38.p7	19:874644	CCCCAGGAGTAGAGA[C/G]AGGTGAAAGGATCGC	10025
rs151223970	snp	C/T	0.000155988	0.00883005	missense	MED16	GRCh38.p7	19:872043	CCCAGATGCGGATGA[C/T]CACCATCAATTCCCG	10025
rs151247622	snp	C/T	0.00835141	0.0640778	intron-variant	MED16	GRCh38.p7	19:881979	GCACCATCTCACCCC[C/T]GATGGGGCAGACAGT	10025
rs180680089	snp	C/T	0.00358779	0.0422022	downstream-variant-500B	MED16	GRCh38.p7	19:867697	GAAACAAGGAGAGCA[C/T]GCAGAGACAGTATAG	10025
rs180695833	snp	A/G	0.00199481	0.0315187	intron-variant	MED16	GRCh38.p7	19:888297	GAGGCTGAGGCAGAC[A/G]GATCACCTGAGGTGA	10025
rs180750160	snp	A/G	0.00317474	0.0397151	intron-variant	MED16	GRCh38.p7	19:871667	TGTGCTAGGAACTGG[A/G]GAAATAGCAGATATC	10025
rs180764132	snp	C/T	0.0023933	0.0345097	intron-variant	MED16	GRCh38.p7	19:881897	TCGTGCCTCGGCCAC[C/T]CATTGGTTCCAGGAT	10025
rs181364204	snp	A/G	0.00874735	0.0655527	intron-variant	MED16	GRCh38.p7	19:885148	CCCTCGGGCCCTCCT[A/G]GATTCCAGCCCAGGC	10025
rs181380270	snp	A/G	0.00795532	0.062565	intron-variant	MED16	GRCh38.p7	19:869737	CTGGAGGTTCACTTC[A/G]TTTTCTTCCTTTTGC	10025
rs181441851	snp	A/G			intron-variant	MED16	GRCh38.p7	19:873075	AGGGCTCCGAGGTGG[A/G]GGAGGGCTCCGAGGT	10025
rs181488625	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:869897	CCACTTCCTGACCGC[A/G]TGACCCCAGATGAGT	10025
rs181500346	snp	A/C	0.366473	0.221211	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:892916	GCGCCCCGCGCCCCG[A/C]GCCCCGCGCCCCGCG	10025
rs181612781	snp	C/T			intron-variant	MED16	GRCh38.p7	19:878141	CCTGGTTGTCAATGC[C/T]CAGCAGCTCACCTTC	10025
rs181857873	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:885451	GAGACGGGAGAGCAC[A/G]TTGGGGGGGGTCCGG	10025
rs181863571	snp	A/G			intron-variant	MED16	GRCh38.p7	19:873111	AGGGCTCCGAGGTGG[A/G]GCAGGGCTCCGAGAT	10025
rs181989679	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:874620	GTGTCGGCCTGGGAG[C/T]GTCTCAGCCCCCAGG	10025
rs181993400	snp	C/T	0.000501148	0.015823	synonymous-codon	MED16	GRCh38.p7	19:871984	GCTGTCCTGGGTATC[C/T]GAGGTGGCCGTATAC	10025
rs181994783	snp	A/G	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:888065	AAAAAGCAGCCGGGC[A/G]TGGTGGCGGGCGCCT	10025
rs182049695	snp	A/C/T	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:877430	CGAGCCAGGCTTACA[A/C/T]TCGTCTGCTTTACCT	10025
rs182063297	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:883243	GAAGCCTGGCATGGT[A/G]GGCACGTGGGGCGGT	10025
rs182069989	snp	C/T	0.00835141	0.0640778	intron-variant	MED16	GRCh38.p7	19:872594	GGCCCCAGGGCAGGA[C/T]GAAGCCGGGTGGGTG	10025
rs182352213	snp	C/T	0.00755907	0.0610114	intron-variant	MED16	GRCh38.p7	19:869634	AGAGCCAAGCCAGGG[C/T]GCCTTCCCGGAGGTC	10025
rs182404731	snp	C/T	0.00716266	0.059414	intron-variant	MED16	GRCh38.p7	19:868612	CGTCCCTCACGCCTG[C/T]TCCCCACGTCCCCAC	10025
rs182449054	snp	C/T	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:882942	AGTGGCTGAGACGCC[C/T]AGAGGGCACACAGTG	10025
rs182583402	snp	G/T	0.00438332	0.0466095	intron-variant	MED16	GRCh38.p7	19:870656	AGAAGACACCACTAG[G/T]GGATGGAGTTAGGGG	10025
rs182595854	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:880437	CCCTCAAGGAGCGCA[A/G]GGGAGGGGGGCACTA	10025
rs182614792	snp	G/T			upstream-variant-2KB, downstream-variant-500B	MED16, RNU6-9	GRCh38.p7	19:893812	ATGTTGGCCAGGGTG[G/T]TCTCTATCTACTGAC	10025
rs182667690	snp	A/G	0.00159617	0.0282053	utr-variant-3-prime	MED16	GRCh38.p7	19:867975	GCCTGGGCGCAGAGG[A/G]CGTTTATTGGACCTG	10025
rs182671604	snp	C/G	0.00358779	0.0422022	intron-variant	MED16	GRCh38.p7	19:888884	GTTCCTGCGAGAGCC[C/G]CAGCACAAGCAGACG	10025
rs182675080	snp	A/C/G	0.000132247	0.00813068	intron-variant	MED16	GRCh38.p7	19:875460	TGGAGAGGACCTGAG[A/C/G]GCAGGAAGCCAGGTC	10025
rs182721826	snp	A/G	9.61677e-05	0.00693359	synonymous-codon, utr-variant-5-prime	MED16	GRCh38.p7	19:890192	CTCTGAGGGGATCGA[A/G]TGCAGGTCCCAGGGG	10025
rs182877534	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:873726	GGAACGAGAAGGGGG[C/T]GATGGCGTTGCCGGA	10025
rs182887168	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:886654	TGCAGACCTGAGCTA[C/T]AGCACTCAGGAAGTG	10025
rs182905956	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:883557	GACCCCCAGCTGCCA[A/G]GGATGTGAGACCTGA	10025
rs183055782	snp	C/G			intron-variant	MED16	GRCh38.p7	19:873149	GGCTCCGAGGTGGGG[C/G]AGGGCTAGGAAGTGG	10025
rs183181178	snp	A/G	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:872787	GAGGGTAAGGGGTGG[A/G]GGCAGCAGCAGCAGA	10025
rs183232687	snp	C/G			intron-variant	MED16	GRCh38.p7	19:870546	AGCCTGGGCAACAGA[C/G]TGAGACCCTGTCGGG	10025
rs183315529	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:886948	GCCGGGCATGGTAGC[A/G]GGTGCCTATAATCCC	10025
rs183343677	snp	A/G	0.000399281	0.0141238	synonymous-codon	MED16	GRCh38.p7	19:886006	AGGCGATGTCGGCCA[A/G]GGCCACGCGGCCGCG	10025
rs183479211	snp	A/G	0.0023933	0.0345097	intron-variant	MED16	GRCh38.p7	19:884108	CCACCTGCCCCACGT[A/G]CCCCCACGTCTGGCC	10025
rs183780401	snp	A/G	0.000393352	0.0140186	missense	MED16	GRCh38.p7	19:880010	TTTAAGTGGACGGCG[A/G]GGCCCGCGGTGCGGG	10025
rs183905196	snp	A/G	0.00597247	0.0543191	intron-variant	MED16	GRCh38.p7	19:869091	GTCTGTGAACAGTGA[A/G]GTGGGAGGTGCGGGA	10025
rs183920280	snp	A/G	0.000511378	0.0159821	synonymous-codon, intron-variant	MED16	GRCh38.p7	19:877154	CAGCGGGTGGCCCAT[A/G]GAAGGTGAGAGGCGG	10025
rs183937872	snp	A/C			intron-variant	MED16	GRCh38.p7	19:890440	TGTGAGGCGCCACAA[A/C]TGTGTCTTTAAAACC	10025
rs183947686	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:884707	TGGAGGAGTCTATAC[A/G]CCTAACACACTCAGA	10025
rs183949307	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:876424	AGGGCCACCGGGTGT[A/G]CATCCTGGTACCCAT	10025
rs183952702	snp	A/C			intron-variant	MED16	GRCh38.p7	19:873012	AGGTGGGGGAGGGCT[A/C]CGAGGTGGGGCAGGG	10025
rs183955762	snp	A/C/T	0.00398564	0.0444627	upstream-variant-2KB, nc-transcript-variant	MED16, RNU6-9	GRCh38.p7	19:893538	TACAGAGAAGATTAG[A/C/T]ATGGCCCCTGCGCAA	10025
rs183980682	snp	A/G	0.00159617	0.0282053	intron-variant	MED16	GRCh38.p7	19:874079	CCAGGAGTGCCACGT[A/G]TCCACACTCAACCGG	10025
rs184187263	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:882111	CCAATAAAGCCATGC[A/G]GGATGGTCGCACCCA	10025
rs184492200	snp	C/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:887945	CAGTGACTCACGCCT[C/G]TCATCCCAGCACTTT	10025
rs184496223	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:874373	CGCGTTGGCCTCCCA[A/G]AGTGCTGGGATTACA	10025
rs184541209	snp	C/T	6.85448e-05	0.00585386	intron-variant	MED16	GRCh38.p7	19:891153	AGTCACCAGCTCCTG[C/T]GGGAGGGAGGTGTGG	10025
rs184609942	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:885098	GGGACCCTGGGGCCA[C/T]GCACTGCTGGGCCTG	10025
rs184678056	snp	C/T			intron-variant	MED16	GRCh38.p7	19:877485	GTCCTCTCAACAGCT[C/T]CTAGTTACGAAGCTC	10025
rs184826848	snp	C/G	0.000547495	0.0165363	intron-variant	MED16	GRCh38.p7	19:873049	GGTGGGGCAGGGCTC[C/G]GAGGTGGGGCAGGGC	10025
rs184840255	snp	A/G	0.00223821	0.033378	intron-variant	MED16	GRCh38.p7	19:871301	CCTGACTGGGGCACC[A/G]CCCGGCCACCCGGGA	10025
rs184865025	snp	C/G	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:881795	AGTCCAGCATGGCCT[C/G]GTGTGCAACCTGCCC	10025
rs184870025	snp	A/G	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:874303	ATTTTTAGTAGAGAC[A/G]GGGTTTCACCGTGTT	10025
rs184895820	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:887116	AAGAAAAATGTCTCT[A/G]CGTTGTGAAAAAATG	10025
rs184987251	snp	C/G	0.375	0.216506	intron-variant	MED16	GRCh38.p7	19:872969	GGCTCCGAGGTGGGG[C/G]AGGGCTCCGAGGTGG	10025
rs185192086	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:885688	CCCGTGGAGGCCCGC[A/G]CGGGTCTCCACCCCC	10025
rs185330640	snp	A/G	0.0225045	0.103662	intron-variant	MED16	GRCh38.p7	19:870815	CAGGACATGGAGGGA[A/G]GGAGCCGTGTGGATT	10025
rs185330765	snp	C/T	0.00914312	0.0669923	upstream-variant-2KB	MED16	GRCh38.p7	19:895040	GCAGTGAGCTGAGAT[C/T]GCGCCACTGCACTCC	10025
rs185442319	snp	C/T	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:881317	GTTGATTTGCAATGA[C/T]TCTTTACATATTAAA	10025
rs185494944	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:869643	CCAGGGCGCCTTCCC[A/G]GAGGTCCCGGAGCCA	10025
rs185554705	snp	C/T	0.0023933	0.0345097	intron-variant	MED16	GRCh38.p7	19:877339	CTGTAGCGTCTGTAC[C/T]TTTCTGTCAGGGTCA	10025
rs185557315	snp	C/G/T	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:869810	CTCAGAGGGTTTGCA[C/G/T]GTGCTCCTTGTCAAA	10025
rs185697844	snp	C/T	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:869551	TTCCTGAAACCCAAA[C/T]CCTCGTGTGTGACTC	10025
rs185711626	snp	A/G	0.0205511	0.0992634	intron-variant	MED16	GRCh38.p7	19:890590	ATGACCACGTATTAT[A/G]AGTGCCTATTACTCA	10025
rs185737415	snp	A/G	0.00318978	0.0398085	downstream-variant-500B	MED16	GRCh38.p7	19:867893	AAGACAGGCCAAGAG[A/G]ACACAGGCTCCCGGC	10025
rs186062227	snp	C/G			intron-variant	MED16	GRCh38.p7	19:873113	GGCTCCGAGGTGGGG[C/G]AGGGCTCCGAGATGG	10025
rs186193269	snp	C/T	0.00162442	0.028453	utr-variant-3-prime	MED16	GRCh38.p7	19:868057	AGGAAACCGAGGAGA[C/T]GCCCGAGCCGGGTCA	10025
rs186207891	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:889227	CTTACCTGTGGGGCC[A/G]AATCACAGGGAGCAT	10025
rs186214692	snp	C/T	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:876146	ATGGGATTTTTTTTT[C/T]CCCATTTTATCTTCG	10025
rs186249563	snp	A/G	0.00398564	0.0444627	intron-variant	MED16	GRCh38.p7	19:886376	CCCCTCTGACCCTCC[A/G]TCTCCTCATCTGTAA	10025
rs186270419	snp	C/G			intron-variant	MED16	GRCh38.p7	19:873077	GGCTCCGAGGTGGGG[C/G]AGGGCTCCGAGGTGG	10025
rs186280065	snp	C/T			intron-variant	MED16	GRCh38.p7	19:885184	CCCAGAGCCCAACAT[C/T]CACTCACAGGAACGC	10025
rs186375484	snp	G/T			intron-variant	MED16	GRCh38.p7	19:875140	CTGCACTCCAGCCTG[G/T]GCAACAGAGTAAGAC	10025
rs186596242	snp	G/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:888725	CCGCAGGGTGGGGAG[G/T]GCACCCCGGAGGGCC	10025
rs186618315	snp	A/G	0.00199481	0.0315187	intron-variant	MED16	GRCh38.p7	19:883256	GTGGGCACGTGGGGC[A/G]GTGCGTGAAGAGCTG	10025
rs186627660	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:868691	TCCCTGAACTAGCCC[C/T]GCCACACCAAGTTAA	10025
rs186638145	snp	A/G	0.000136509	0.00826051	synonymous-codon, intron-variant	MED16	GRCh38.p7	19:877076	GATGTCCCACCAGTC[A/G]TAGCCGGTCACCATG	10025
rs186773580	snp	A/G	0.000137399	0.00828738	missense	MED16	GRCh38.p7	19:880016	TGGACGGCGGGGCCC[A/G]CGGTGCGGGGGCGCT	10025
rs186828027	snp	A/G	0.0103295	0.0711199	intron-variant	MED16	GRCh38.p7	19:880782	AAAAATTAGCCGGGC[A/G]TGGCAGCACGCGCCT	10025
rs186845131	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	MED16	GRCh38.p7	19:894461	TAGGCGTGAGCCACC[A/G]CGGCCTCACTGCATG	10025
rs186905378	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:870695	AGGAAGCAGCAGTCA[C/T]GGCCATGACTGGAGA	10025
rs186907274	snp	A/G			intron-variant	MED16	GRCh38.p7	19:877734	GCCCCACGTGCCCCA[A/G]CAGCTCACCTTCCCC	10025
rs186916701	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:893344	TTTCTCAACTCCAGT[C/T]AATAACTACGTTAGT	10025
rs186977092	snp	A/C			intron-variant	MED16	GRCh38.p7	19:871868	GCGGGGAGCGGGGAG[A/C]GGGGAGAGGGGAGAG	10025
rs187058619	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:888205	CAAGACCCTGTCTCA[A/G]AAAACAAACAAACAA	10025
rs187078000	snp	C/G	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:882613	AGGGCAGCTGGAGCC[C/G]GCCTGCTGGAGCATG	10025
rs187132475	snp	C/T	0.000798403	0.0199641	downstream-variant-500B	MED16	GRCh38.p7	19:867532	GGACAGCAACAGAAA[C/T]GGCAGAAACTTGGCC	10025
rs187217898	snp	A/G			intron-variant	MED16	GRCh38.p7	19:878989	CACCTTCCCCTGGCT[A/G]TCAATGCCCACCAGC	10025
rs187236132	snp	C/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:874873	AGACCGTCTCTAAAA[C/G]CCTGGGTGTGGTGTA	10025
rs187429485	snp	A/G	0.00562235	0.0527216	intron-variant	MED16	GRCh38.p7	19:877205	ACAGAGCCCAAGGAG[A/G]GCCCGGTGAGATGGG	10025
rs187437865	snp	A/G	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:870065	AGAAAGGCCAGCCCC[A/G]GGCCCTGCAAGGTGA	10025
rs187438493	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:890509	AGCCTCTCCACAGCA[A/G]ATAATAGGTGGCTTT	10025
rs187493353	snp	C/G	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:886678	GGAAGTGCTGTGTAA[C/G]CACCAGCGGCTGCTG	10025
rs187495551	snp	A/G	0.00398564	0.0444627	intron-variant	MED16	GRCh38.p7	19:873739	GGCGATGGCGTTGCC[A/G]GACGGAGAGGAACTG	10025
rs187703916	snp	C/T	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:884629	CCGCTGGCTGAGCAA[C/T]GACACCTCTCAGCCT	10025
rs187706856	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	MED16, RNU6-9	GRCh38.p7	19:893549	TTAGCATGGCCCCTG[C/G]GCAAGGATGACACGC	10025
rs187721294	snp	A/G	0.00636936	0.0560724	intron-variant	MED16	GRCh38.p7	19:874208	AAGCTCCGCCTCCCG[A/G]GTTCACGCCATTCTC	10025
rs187847126	snp	C/T	0.000125196	0.00791089	intron-variant	MED16	GRCh38.p7	19:890254	TCAGGTCTGTGGGGA[C/T]GGGGCATGGTCAGCA	10025
rs187922943	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:887054	ATTACACTCTGGCCT[A/G]GGCAACGAGAGCAAA	10025
rs188191480	snp	C/T			intron-variant	MED16	GRCh38.p7	19:869651	CCTTCCCGGAGGTCC[C/T]GGAGCCAAGCCGGGG	10025
rs188207340	snp	A/G			intron-variant	MED16	GRCh38.p7	19:891255	CCCGTGGTAGAGGGA[A/G]CAGCCGATGCAAAGG	10025
rs188207536	snp	C/T			intron-variant	MED16	GRCh38.p7	19:877799	CCAGCCCCAGCCCCA[C/T]GTGCCCCAGCAGCTC	10025
rs188339630	snp	C/T	0.000852118	0.0206236	intron-variant	MED16	GRCh38.p7	19:871557	GAATGACACAGCTCA[C/T]CCTCCTCACATACAC	10025
rs188355485	snp	A/G	0.00358779	0.0422022	intron-variant	MED16	GRCh38.p7	19:881862	TGCCCAGAAGACCAG[A/G]CCCGGCCAATCCGAG	10025
rs188504125	snp	A/G	0.0138799	0.0821421	intron-variant	MED16	GRCh38.p7	19:872816	GAAGCAAGGCGAACC[A/G]GCCTTCGTGTAGGGG	10025
rs188589823	snp	G/T	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:889500	CAGGTGCTAATGACA[G/T]CCGGACTGCAGGTGG	10025
rs188643262	snp	A/G	0.00676609	0.0577691	intron-variant	MED16	GRCh38.p7	19:870894	GGGGGTCCCGGGCAG[A/G]ACATGGAGGCGGGGA	10025
rs188653862	snp	A/G	0.00428134	0.0460689	intron-variant	MED16	GRCh38.p7	19:868355	GGTAGCTGAGGAGTA[A/G]CTGAGGGGCAGCTGG	10025
rs188803267	snp	A/G	0.00597247	0.0543191	intron-variant	MED16	GRCh38.p7	19:883706	TGGCTGTGGGCAGAT[A/G]GTAGACACAGACGTG	10025
rs188846136	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:887975	TGGGAGGCCAAGACA[A/G]GCAGATCACCTGAGG	10025
rs188852622	snp	A/C	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:874487	TTTGGGAGGCAGAGG[A/C]GAGTAGGACACCACG	10025
rs188944139	snp	C/T			intron-variant	MED16	GRCh38.p7	19:876625	TCTGGGAGCACACCC[C/T]ACACGCAGCCTCACC	10025
rs189072618	snp	A/G	0.00438332	0.0466095	intron-variant	MED16	GRCh38.p7	19:869247	GGGTCGGTCCGCCAC[A/G]TGCCCGGGGAGCCTG	10025
rs189081677	snp	A/G			intron-variant	MED16	GRCh38.p7	19:884794	AGACGATCGCTTAGG[A/G]CCGGGGTTCAGGACC	10025
rs189398061	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:887487	CCTGGCCAAGATAGT[A/G]AAACCCCGTCTCTAC	10025
rs189419980	snp	A/C			intron-variant	MED16	GRCh38.p7	19:871822	GGGGAGAGGGGAGAG[A/C]GGGGAGAGGGGAGAG	10025
rs189451121	snp	A/G			intron-variant	MED16	GRCh38.p7	19:873016	GGGGGAGGGCTCCGA[A/G]GTGGGGCAGGGCTCC	10025
rs189475907	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:885427	GGGTGGGATTCGGTT[C/T]GGGACACTGAGACGG	10025
rs189481831	snp	C/G	0.00134138	0.0258629	intron-variant	MED16	GRCh38.p7	19:873095	GGCTCCGAGGTGGGG[C/G]AGGGCTCCGAGGTGG	10025
rs189519987	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	MED16	GRCh38.p7	19:867685	CAGAGACACGCAGAA[A/G]CAAGGAGAGCACGCA	10025
rs189553589	snp	C/T	0.00159617	0.0282053	intron-variant	MED16	GRCh38.p7	19:888296	GGAGGCTGAGGCAGA[C/T]GGATCACCTGAGGTG	10025
rs189578001	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:880347	ACCAGGGGAGCAGGA[A/G]CCAGCAGCCTTGGCC	10025
rs189587266	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB, downstream-variant-500B	MED16, RNU6-9	GRCh38.p7	19:893608	TTTTTTTTCCATTTT[C/T]CCTCCCAGAAACGGA	10025
rs189660327	snp	A/G			intron-variant	MED16	GRCh38.p7	19:870609	GAATGGAAGGGCTGG[A/G]TGCCCGTGTTGGGGG	10025
rs189671514	snp	A/C/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:874320	GGTTTCACCGTGTTA[A/C/G]CCAGGATGATCTCGA	10025
rs189693160	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:882126	GGGATGGTCGCACCC[A/G]CAGATCCGCTGCCTG	10025
rs189716416	snp	A/G	0.00159617	0.0282053	intron-variant	MED16	GRCh38.p7	19:883029	CAACGCCCCAGCGCC[A/G]GGGGAGGCAGCTGCC	10025
rs189800958	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:872482	CTGAGAGGACCAGGG[A/G]AGGGAGGCCCCAGGG	10025
rs190223996	snp	C/T	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:869555	TGAAACCCAAACCCT[C/T]GTGTGTGACTCATTA	10025
rs190226024	snp	C/T			intron-variant	MED16	GRCh38.p7	19:890718	CCGTCAACCAACGCT[C/T]CAGCCCGATTCGATC	10025
rs190322944	snp	A/G	0.0103295	0.0711199	intron-variant	MED16	GRCh38.p7	19:885101	ACCCTGGGGCCACGC[A/G]CTGCTGGGCCTGTCT	10025
rs190400796	snp	A/G	0.00318978	0.0398085	downstream-variant-500B	MED16	GRCh38.p7	19:867906	AGGACACAGGCTCCC[A/G]GCACCAAATCGAGGT	10025
rs190408350	snp	G/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:888832	AGGGACGAGAGAAAA[G/T]ATCTTGTCCACTGCA	10025
rs190464121	snp	A/C	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:877397	GAAACCTCCCTGAGC[A/C]CCGACTGCACTGGAT	10025
rs190499253	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:889333	CAGCTACCTAAGGAC[A/G]GTAGCCTCCAGTGAA	10025
rs190583475	snp	A/G	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:876327	GGCACGTGGGCCTCC[A/G]TATCCGCTCCCTCCT	10025
rs190646188	snp	A/C			intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:892909	GCGCCCCGCGCCCCG[A/C]GCCCCGCGCCCCGCG	10025
rs190724154	snp	A/C			intron-variant	MED16	GRCh38.p7	19:878081	TGGCTGTCAATGCCC[A/C]CCAGCCCCAGCCCCA	10025
rs190727221	snp	A/G	0.000203995	0.0100973	synonymous-codon	MED16	GRCh38.p7	19:885944	CTGCACGGGCGACGC[A/G]CTGCTGCCGTCCGCC	10025
rs191055201	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:889879	GCAGGACGGCACAGC[A/G]CCTGGGGGAAGCCAG	10025
rs191363604	snp	C/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:872723	GAAGGTGGAGGTGTG[C/G]ATGGAGACTTGATTT	10025
rs191467039	snp	A/G	0.00159617	0.0282053	intron-variant	MED16	GRCh38.p7	19:884652	CTCAGCCTCGGCCTC[A/G]CACAGAATGGTGGCA	10025
rs191475289	snp	A/G			intron-variant	MED16	GRCh38.p7	19:873001	GGAGGGCTCCGAGGT[A/G]GGGGAGGGCTCCGAG	10025
rs191512176	snp	C/T	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:882676	TGCTAACCGCAGACA[C/T]GTGGGAACCAGGAGA	10025
rs191602968	snp	C/G	0.00795532	0.062565	intron-variant	MED16	GRCh38.p7	19:883492	GTGGGCACGTGGGGC[C/G]GTAGGGGGAGAGATG	10025
rs191632722	snp	C/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:887749	AGGACATCACGCTCA[C/G]TAAGAGATGCCAGAC	10025
rs191639025	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:874347	TCGATCTCCTGACCT[C/T]GTGATCAGCCCGCGT	10025
rs191758226	snp	A/C	0.286825	0.247273	intron-variant	MED16	GRCh38.p7	19:871898	GCGGGGAGCGGGGAG[A/C]GGGGAGGGGCGGGCG	10025
rs191791821	snp	C/G	0.00244319	0.0348658	intron-variant	MED16	GRCh38.p7	19:890331	GCTCCAGGTAAGCCG[C/G]TGTGTGTCCCACCCC	10025
rs191791872	snp	A/C/G	3.5024e-05	0.00418461	synonymous-codon, intron-variant	MED16	GRCh38.p7	19:877109	GTACTCCAGCAGGAA[A/C/G]AGCAGGTGCCGCAGC	10025
rs191841923	snp	A/G			intron-variant	MED16	GRCh38.p7	19:871390	TGGCTGGGTGACCCC[A/G]GGGTTCTCTCACCAG	10025
rs191871635	snp	C/T	0.00398564	0.0444627	intron-variant	MED16	GRCh38.p7	19:869047	GAGGGAATGGCCGGC[C/T]TCACACCATCTGCCA	10025
rs191887647	snp	A/G	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:886388	TCCGTCTCCTCATCT[A/G]TAAGGTGGAAGGAAC	10025
rs191955001	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:869875	CTGGGTTCAAATCCT[A/G]ACTCGGCCACTTCCT	10025
rs191983588	snp	G/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:890518	ACAGCAGATAATAGG[G/T]GGCTTTTTTGCACCC	10025
rs192010590	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:872862	GCAGGGCCTGGGAGG[C/T]GGGGCTTTGAGAATG	10025
rs192104639	snp	A/G	0.00358779	0.0422022	intron-variant	MED16	GRCh38.p7	19:870112	GATCCTCCTGATGAG[A/G]TGTCTGCTCAGCAGG	10025
rs192111697	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	MED16, RNU6-9	GRCh38.p7	19:893533	AACGATACAGAGAAG[A/G]TTAGCATGGCCCCTG	10025
rs192144716	snp	A/G	0.00199481	0.0315187	upstream-variant-2KB	MED16	GRCh38.p7	19:894803	TGGGGAGGGAGGGGC[A/G]CTGGGCAAGGTGGTT	10025
rs192338814	snp	C/G	0.0023933	0.0345097	intron-variant	MED16	GRCh38.p7	19:876707	CCTGCCGCAGGGAAA[C/G]CCCTCCAGCTGCCAC	10025
rs192473654	snp	A/G			intron-variant	MED16	GRCh38.p7	19:878916	TTGTCAATGTCCACC[A/G]GCCCCGGCCCCGGCC	10025
rs192495047	snp	A/G			intron-variant	MED16	GRCh38.p7	19:879099	GTGCCCCAGCAGCTC[A/G]CCTTCCCCTGGTTGT	10025
rs192591069	snp	C/T	0.00914312	0.0669923	intron-variant	MED16	GRCh38.p7	19:874270	AGGCGCCCGCCACCA[C/T]GCCCGGCTGATTTTT	10025
rs192692625	snp	A/G/T	0.0127144	0.0788679	intron-variant	MED16	GRCh38.p7	19:886835	AATCCCAGCACTTTG[A/G/T]GGGGCTGAGGCAGGT	10025
rs192695824	snp	A/G	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:873941	GGGCATGTCCACAGC[A/G]TGCAGCTGCAGCCAC	10025
rs192722231	snp	C/T	0.00137092	0.0261453	synonymous-codon	MED16	GRCh38.p7	19:868454	CTCCCACTGCTTCAC[C/T]GCCGTGGTTCTGTTG	10025
rs192764953	snp	A/G			intron-variant	MED16	GRCh38.p7	19:873019	GGAGGGCTCCGAGGT[A/G]GGGCAGGGCTCCGAG	10025
rs192836310	snp	A/G	0.00159617	0.0282053	intron-variant	MED16	GRCh38.p7	19:869513	GCCTCTGACGTAACC[A/G]TCCTCTCTTTCCATC	10025
rs192840639	snp	A/G	0.00358779	0.0422022	intron-variant	MED16	GRCh38.p7	19:883872	CAACAAGGCCCTGGG[A/G]ACCGGGCGAAGGAAC	10025
rs192917820	snp	C/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:880807	GCGCCTGTAGTCCCA[C/G]CTACTCGGGAGGCTG	10025
rs192978124	snp	C/T	0.000387797	0.0139193	intron-variant	MED16	GRCh38.p7	19:885050	GACCCGGCACTGCTG[C/T]GGTGGCCACGCCACC	10025
rs193048588	snp	C/G/T	0.00211358	0.0324412	intron-variant	MED16	GRCh38.p7	19:877209	AGCCCAAGGAGAGCC[C/G/T]GGTGAGATGGGGCTG	10025
rs193163647	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:870808	CCCGGGGCAGGACAT[A/G]GAGGGAGGGAGCCGT	10025
rs193282880	snp	A/G	0.000397288	0.0140885	intron-variant	MED16	GRCh38.p7	19:881744	GCAGGAAAACAGGAA[A/G]GCAATGGAGTAAAGA	10025
rs199512400	snp	A/C/G/T	0.000298068	0.012205	missense, utr-variant-5-prime	MED16	GRCh38.p7	19:891094	ACGTAGGCCAAGTCC[A/C/G/T]TCATCCCACCTGCCG	10025
rs199528280	snp	A/G	0.000320607	0.0126571	missense	MED16	GRCh38.p7	19:868473	GTGGTTCTGTTGGGC[A/G]ACTTGAGCATGGTGA	10025
rs199591635	snp	A/G			intron-variant	MED16	GRCh38.p7	19:879328	CAAGCCCAGCCCCAC[A/G]TGCCCCAGCAGCTCA	10025
rs199592606	snp	A/G	3.33907e-05	0.00408586	missense	MED16	GRCh38.p7	19:881645	GGCAGCGCCACGGCC[A/G]ACACACGGTCCAGAT	10025
rs199605392	snp	C/G	0.00199796	0.0315434	missense, intron-variant	MED16	GRCh38.p7	19:889761	GTGGTCCGCCATGCT[C/G]CAGCACTTGATCTGC	10025
rs199606023	snp	A/C/G	6.57943e-05	0.0057353	intron-variant	MED16	GRCh38.p7	19:868262	CAGCCCTGCAGGGCG[A/C/G]GCTGAGGTTAACCGC	10025
rs199616233	snp	A/C	0.00163934	0.0285829	intron-variant	MED16	GRCh38.p7	19:889836	GCCATCATTGCGAAC[A/C]TTCCAGGGATGGGCA	10025
rs199621954	in-del	-/G			intron-variant	MED16	GRCh38.p7	19:878178	TTGTCAATGCCCACC[-/G]AGCCCAGCCCCACGT	10025
rs199651341	snp	A/G			intron-variant	MED16	GRCh38.p7	19:873733	GAAGGGGGCGATGGC[A/G]TTGCCGGACGGAGAG	10025
rs199716714	snp	A/C	0.00299546	0.0385844	synonymous-codon	MED16	GRCh38.p7	19:884955	GAGTCCCTCCTTGCG[A/C]AGGGACCAGCACTCC	10025
rs199736171	in-del	-/AG			intron-variant	MED16	GRCh38.p7	19:880296	CAGCGCCCGTGCCCC[-/AG]CAGCCACTCTTTCTT	10025
rs199765164	snp	A/G	1.66957e-05	0.00288922	synonymous-codon	MED16	GRCh38.p7	19:875374	GAAGAGCTTGGTGTG[A/G]TAGTCGCACACGCGG	10025
rs199777946	in-del	-/CC			intron-variant	MED16	GRCh38.p7	19:877292	CTGTGTGCGCGCACG[-/CC]CCCGTGTGTGGGCCT	10025
rs199801344	snp	C/G			intron-variant	MED16	GRCh38.p7	19:879855	GCAGCTCACCTTCCC[C/G]TGGTTGTCAATGCCC	10025
rs199813748	snp	A/C/G	0.000410355	0.0143183	intron-variant	MED16	GRCh38.p7	19:890932	GGACACCATGCGGCC[A/C/G]GGAGGGGAAGCAGGT	10025
rs199827624	snp	G/T	0.00230848	0.0338956	intron-variant	MED16	GRCh38.p7	19:876958	CCACGGGGCCCCACC[G/T]GCCACGGGCCCCCAC	10025
rs199831785	snp	A/C/G	0.000354846	0.0133155	missense	MED16	GRCh38.p7	19:872114	CCCGGCCTCAGCAGG[A/C/G]AACCCTGCCCGAAAG	10025
rs199854986	snp	C/G	0.00299553	0.0385849	synonymous-codon	MED16	GRCh38.p7	19:875392	GTCGCACACGCGGGT[C/G]ACCGTGCAGGGCGAC	10025
rs199855041	snp	A/G/T	0.000520012	0.0161165	synonymous-codon	MED16	GRCh38.p7	19:875272	CTTGGTGCAGATCTC[A/G/T]GTCAGCCGGTCGCCG	10025
rs199862268	in-del	-/G	0.00318978	0.0398085	intron-variant	MED16	GRCh38.p7	19:877369	ATGCACAATGCCTCT[-/G]GGAACAGGGAAGGAA	10025
rs199867125	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:873420	GGGCCCAGGTGGGGG[A/G]CGGGGCCTTAGGGGA	10025
rs199940174	snp	C/T			intron-variant	MED16	GRCh38.p7	19:877753	CTCACCTTCCCCTGG[C/T]TGTCAATGCCCACCA	10025
rs199957968	snp	C/T			intron-variant	MED16	GRCh38.p7	19:870589	AAAAAAAAAAGGGAG[C/T]GGGTGAATGGAAGGG	10025
rs200008779	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:889861	TGGGCAGAGCACTGC[A/G]TTGCAGGACGGCACA	10025
rs200085016	snp	C/T	0.00428097	0.0460669	missense	MED16	GRCh38.p7	19:879947	CTCACCTTCCCGTGG[C/T]TGTCAATCCCCACCA	10025
rs200088634	snp	C/G/T	0.000226196	0.0106325	intron-variant	MED16	GRCh38.p7	19:877196	CTGCCAGAGACAGAG[C/G/T]CCAAGGAGAGCCCGG	10025
rs200093557	snp	A/G	8.67762e-05	0.00658639	intron-variant	MED16	GRCh38.p7	19:885748	AGCCTGCCAGCCCAC[A/G]TGATGGCCTGCGCCC	10025
rs200116945	snp	A/G	0.00152512	0.0275723	intron-variant	MED16	GRCh38.p7	19:868412	CCACCAGAGCCCACC[A/G]CACAGGCAGTTCTTG	10025
rs200129542	in-del	-/CGT			intron-variant	MED16	GRCh38.p7	19:877780	CCAGCCCCAGCCCCA[-/CGT]GCCCCAGCCCCAGCC	10025
rs200141305	snp	C/T	8.61067e-05	0.00656094	synonymous-codon	MED16	GRCh38.p7	19:885959	GCTGCTGCCGTCCGC[C/T]GTGGCCACCACGATG	10025
rs200150591	in-del	-/C	0.030278	0.119257	intron-variant	MED16	GRCh38.p7	19:889185	GCCTATCTTAACTGT[-/C]CCCCCCCAACCCTGG	10025
rs200153776	snp	A/G			intron-variant	MED16	GRCh38.p7	19:871850	GAGCGGGGAGAGGGG[A/G]GAGCGGGGAGCGGGG	10025
rs200159274	snp	C/T	0.00318502	0.039779	intron-variant	MED16	GRCh38.p7	19:868849	GGGAGTCAGCGGTTC[C/T]GGGGGCCCCTCACCT	10025
rs200174652	snp	A/C/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:871263	CGCGACCTGCGGAGA[A/C/G]AGGTGGCGGAAGTCT	10025
rs200186933	snp	A/C/G	0.000599662	0.0173055	utr-variant-3-prime	MED16	GRCh38.p7	19:868096	TCCGCCTGGACCCCC[A/C/G]GCCGTCACGGACGGT	10025
rs200212867	snp	A/G	0.000501211	0.0158226	missense	MED16	GRCh38.p7	19:873516	AAGAGCTGCTGCAGC[A/G]CCTGCAGTGTGTTCA	10025
rs200217505	snp	A/C			intron-variant	MED16	GRCh38.p7	19:871813	AGGGAGAGCGGGGAG[A/C]GGGGAGAGCGGGGAG	10025
rs200219839	snp	C/T	0.00119652	0.0244301	intron-variant	MED16	GRCh38.p7	19:873410	GATGAGATGGGGGCC[C/T]AGGTGGGGGGCGGGG	10025
rs200224097	in-del	-/GGGCCAC			intron-variant	MED16	GRCh38.p7	19:879539	TGTCAATGCCTACCA[-/GGGCCAC]GCCCCAGCAGCTCGC	10025
rs200225868	snp	A/G	0.000399281	0.0141238	missense	MED16	GRCh38.p7	19:875429	CAGAGCGAGGCCTTC[A/G]TGGCCAGGATCCGGG	10025
rs200263136	snp	C/G	0.00199796	0.0315434	missense	MED16	GRCh38.p7	19:871977	GGGACATGCTGTCCT[C/G]GGTATCCGAGGTGGC	10025
rs200294634	snp	A/G	0.000251752	0.0112166	synonymous-codon	MED16	GRCh38.p7	19:881584	GTAGAACTGTGTGTC[A/G]CTGGCCACCTTGAGG	10025
rs200309112	in-del	-/AGCCAC					GRCh38.p7	19:878618	TTGTCAACGCCCACC[-/AGCCAC]AACCCCAGCCCCACG	10025
rs200325040	snp	A/C	1.67559e-05	0.00289442	synonymous-codon	MED16	GRCh38.p7	19:875278	GCAGATCTCGGTCAG[A/C]CGGTCGCCGGGGCTC	10025
rs200423465	snp	C/T	1.66946e-05	0.00288912	synonymous-codon	MED16	GRCh38.p7	19:881644	GGGCAGCGCCACGGC[C/T]GACACACGGTCCAGA	10025
rs200435606	snp	A/G	0.00124992	0.0249679	intron-variant	MED16	GRCh38.p7	19:868258	TCAACAGCCCTGCAG[A/G]GCGGGCTGAGGTTAA	10025
rs200464312	snp	A/C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:874729	CAAAAAATTAAAAAC[A/C/T]GGGTGTGGTGGCACG	10025
rs200531644	snp	C/T	0.000153988	0.00877327	intron-variant	MED16	GRCh38.p7	19:873408	CTGATGAGATGGGGG[C/T]CCAGGTGGGGGGCGG	10025
rs200573504	snp	A/G	8.33549e-05	0.00645527	missense, utr-variant-5-prime	MED16	GRCh38.p7	19:891112	ATCCCACCTGCCGCT[A/G]GCCGCCGCAAATCAC	10025
rs200579290	snp	A/G	0.000399281	0.0141238	missense	MED16	GRCh38.p7	19:871217	CATTCATCCACCAGC[A/G]CCTCGTCCGGCTCGC	10025
rs200712141	snp	A/G	1.65436e-05	0.00287602	synonymous-codon, utr-variant-5-prime	MED16	GRCh38.p7	19:891081	CTCCCACTCACAGAC[A/G]TAGGCCAAGTCCATC	10025
rs200772638	snp	C/T	3.4082e-05	0.00412793	intron-variant	MED16	GRCh38.p7	19:868515	CTGCGGGGAGGCAGG[C/T]ACTGAGCGGGTTCCC	10025
rs200788786	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:890276	TGGTCAGCACGGCCT[A/G]GCACCACAGCCTGCA	10025
rs200805105	in-del	-/ACGT			intron-variant	MED16	GRCh38.p7	19:868965	GCGGGAGAGGGGAGA[-/ACGT]GAGGGAGGCCTGGGC	10025
rs200816964	snp	A/G	0.000409528	0.0143037	missense	MED16	GRCh38.p7	19:871088	CCAGGCAGCGTGGGC[A/G]CCCGGCCAAACTGCA	10025
rs200850152	snp	A/C/G	5.05211e-05	0.00502577	missense, synonymous-codon	MED16	GRCh38.p7	19:873472	GTAGGCTGGCCAGCA[A/C/G]GTACAGCACGAAGTC	10025
rs200913984	in-del	-/CT			intron-variant	MED16	GRCh38.p7	19:889076	CCCTGGCCACGCCTA[-/CT]CTTAACTGTCCCCAA	10025
rs200916270	snp	A/C/T	0.000690414	0.0185672	utr-variant-3-prime	MED16	GRCh38.p7	19:868061	AACCGAGGAGACGCC[A/C/T]GAGCCGGGTCACCAC	10025
rs200919426	snp	A/G	0.000176483	0.00939203	synonymous-codon	MED16	GRCh38.p7	19:880111	TGAGAGCCGGTGCAC[A/G]ATGTGGACGCTGCCG	10025
rs200953187	snp	A/C/T	5.29697e-05	0.00514612	intron-variant	MED16	GRCh38.p7	19:889622	CCTCATCCGCTCACT[A/C/T]GGGCAGGACACTCAC	10025
rs200973969	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:868295	CGAGGAGAGTCCAGG[A/G]CGAGCGGTGGCTCTT	10025
rs200993578	snp	C/T	1.66407e-05	0.00288446	missense, utr-variant-5-prime	MED16	GRCh38.p7	19:890987	CGCTGCGCAGGTCCA[C/T]GGTGAAGGCGATGAG	10025
rs201006271	snp	A/G	0.000486435	0.0155878	intron-variant	MED16	GRCh38.p7	19:872168	CGGGGGGCAGATGGC[A/G]ATGGGATGAAGTGTC	10025
rs201034793	snp	C/T	8.23028e-05	0.00641441	missense	MED16	GRCh38.p7	19:880128	TGTGGACGCTGCCGT[C/T]GTGGAAGGCCAGGGC	10025
rs201061199	snp	C/T	1.69135e-05	0.002908	intron-variant	MED16	GRCh38.p7	19:885767	TGGCCTGCGCCCGTT[C/T]ACCTGCTCCGACATG	10025
rs201064678	in-del	-/CCCAGA			intron-variant	MED16	GRCh38.p7	19:877659	AGCCCCAGCCCCAGC[-/CCCAGA]CCCACGTGCCCCAGC	10025
rs201099093	snp	A/G	0.000600781	0.0173214	intron-variant	MED16	GRCh38.p7	19:873595	TGTCTACAAGGAGAC[A/G]TGGGTCGGGTCAGCT	10025
rs201101329	snp	C/G	0.000598852	0.0172936	synonymous-codon	MED16	GRCh38.p7	19:885851	GAGGTCGGTGGTGCA[C/G]CGCATGAACAGGGAG	10025
rs201103755	snp	A/G	0.00201796	0.0317003	intron-variant	MED16	GRCh38.p7	19:868823	TGAGCCATCCCCAGC[A/G]GCACATCTCTGGGAG	10025
rs201119725	snp	A/G			intron-variant	MED16	GRCh38.p7	19:879763	TGTCAATGCCCACCA[A/G]CCCCAGCCCCACGTG	10025
rs201127060	in-del	-/GCCCAG			intron-variant	MED16	GRCh38.p7	19:877844	GTCAATGCCCACCAA[-/GCCCAG]CCCCACATGCCCCAG	10025
rs201151887	snp	C/T			intron-variant	MED16	GRCh38.p7	19:879302	ACCTTCCCATGGTTG[C/T]CAATGCCCACCAAGC	10025
rs201156340	snp	A/G	0.000399281	0.0141238	synonymous-codon	MED16	GRCh38.p7	19:871042	ACACACGCACCTGGC[A/G]AGGCCGTCGAGCTGC	10025
rs201161227	snp	A/G	3.38771e-05	0.00411551	synonymous-codon	MED16	GRCh38.p7	19:872014	CACGGGCAGGCAGCT[A/G]GGCTTCAGAAGGCCC	10025
rs201215886	snp	A/C/G	4.7129e-05	0.00485414	missense	MED16	GRCh38.p7	19:879965	TCAATCCCCACCAGG[A/C/G]CCAGTGACGTCCACG	10025
rs201235613	snp	C/T	0.0035322	0.0418763	missense, utr-variant-5-prime	MED16	GRCh38.p7	19:891098	AGGCCAAGTCCATCA[C/T]CCCACCTGCCGCTGG	10025
rs201243936	snp	A/G			intron-variant	MED16	GRCh38.p7	19:878646	GCCCCACGTGCCCCA[A/G]CAGCTCACCTTCCCC	10025
rs201267550	in-del	-/T			upstream-variant-2KB, downstream-variant-500B	MED16, RNU6-9	GRCh38.p7	19:893600	TTTTTTTTTTTTTTT[-/T]CCATTTTCCCTCCCA	10025
rs201346217	snp	A/G	0.00494567	0.0494811	intron-variant	MED16	GRCh38.p7	19:879920	CAGCCCCGGCCCCAC[A/G]TGCCCCAGCAGCTCA	10025
rs201386748	snp	C/T	0.00019292	0.00981951	missense, utr-variant-5-prime	MED16	GRCh38.p7	19:890167	CCAGGCAGGTGATGG[C/T]CTCGTGGTGCTCTGA	10025
rs201392672	in-del	-/GTGG			frameshift-variant	MED16	GRCh38.p7	19:879943	GCAGCTCACCTTCCC[-/GTGG]CTGTCAATCCCCACC	10025
rs201431157	snp	A/G	0.00036713	0.0135436	missense	MED16	GRCh38.p7	19:868231	GTCACGCAGGCGTCC[A/G]GCCCACGGCCTTCAA	10025
rs201452972	snp	A/G	0.000101555	0.00712513	intron-variant	MED16	GRCh38.p7	19:868281	GAGGTTAACCGCGCC[A/G]AGGAGAGTCCAGGGC	10025
rs201518892	snp	C/G	0.000574972	0.0169457	synonymous-codon, utr-variant-5-prime	MED16	GRCh38.p7	19:886145	GCCGCCGAACAGCGT[C/G]AGCGACGGTGAGAAC	10025
rs201528745	snp	C/T	0.000108792	0.00737457	intron-variant	MED16	GRCh38.p7	19:889614	CTCATCTGCCTCATC[C/T]GCTCACTCGGGCAGG	10025
rs201531363	snp	C/T	0.00229663	0.0338089	missense	MED16	GRCh38.p7	19:868897	CCTCCGTGGGGCAAG[C/T]GCCAAGGTGCAGCCT	10025
rs201545631	snp	C/T	0.000554309	0.0166387	intron-variant	MED16	GRCh38.p7	19:881510	CTCAGGGCCCAACTC[C/T]CCTGGTGTGAACTGA	10025
rs201573442	snp	C/T	6.68282e-05	0.00578011	synonymous-codon	MED16	GRCh38.p7	19:881671	CAGATCGTTGGTGGC[C/T]GATAGGATCCGCCAT	10025
rs201576382	in-del	-/GGG	0.00874735	0.0655527	intron-variant	MED16	GRCh38.p7	19:883507	GGTAGGGGGAGAGAT[-/GGG]GGAGAGATGGGTGCG	10025
rs201595768	snp	A/C/G	3.33785e-05	0.00408514	intron-variant	MED16	GRCh38.p7	19:873592	CAATGTCTACAAGGA[A/C/G]ACGTGGGTCGGGTCA	10025
rs201600325	snp	C/T	0.000517076	0.0160708	missense	MED16	GRCh38.p7	19:875367	CGATGAGGAAGAGCT[C/T]GGTGTGGTAGTCGCA	10025
rs201618878	snp	A/G	0.000399281	0.0141238	missense	MED16	GRCh38.p7	19:875396	CACACGCGGGTCACC[A/G]TGCAGGGCGACAGCT	10025
rs201640890	snp	A/G	9.79499e-05	0.00699753	synonymous-codon	MED16	GRCh38.p7	19:880018	GACGGCGGGGCCCGC[A/G]GTGCGGGGGCGCTTC	10025
rs201643295	snp	A/G	0.00612327	0.0549922	intron-variant	MED16	GRCh38.p7	19:884865	CCAACCGCCCCCGAG[A/G]GCAGGCCCAGGGCCT	10025
rs201643609	snp	A/G	8.4453e-05	0.00649764	missense	MED16	GRCh38.p7	19:872045	CAGATGCGGATGACC[A/G]CCATCAATTCCCGAA	10025
rs201650556	in-del	-/TAGGGGCGGGACTCCAAC			intron-variant	MED16	GRCh38.p7	19:873324	GGGCGGGACTCCAAG[-/TAGGGGCGGGACTCCAAC]TAGGGGCGGGGCTGA	10025
rs201651884	in-del	-/AGA			intron-variant	MED16	GRCh38.p7	19:871884	GGGAGAGGGGAGAGC[-/AGA]GGGGAGCGGGGAGAG	10025
rs201663010	snp	C/G	0.000100057	0.00707236	missense	MED16	GRCh38.p7	19:873577	TGATCATGACCTTGT[C/G]AATGTCTACAAGGAG	10025
rs201690635	snp	A/G/T	1.78071e-05	0.00298383	synonymous-codon	MED16	GRCh38.p7	19:871963	CAGGCGGAAGAGCAG[A/G/T]GACATGCTGTCCTGG	10025
rs201795216	in-del	-/T			intron-variant	MED16	GRCh38.p7	19:878240	TGCCCACCAGCCCCA[-/T]GCCCCAGCCCCAGCC	10025
rs201805492	snp	A/G			intron-variant	MED16	GRCh38.p7	19:877726	CAGCCCCTGCCCCAC[A/G]TGCCCCAGCAGCTCA	10025
rs201868030	in-del	-/A	0.0217236	0.101931	intron-variant	MED16	GRCh38.p7	19:882345	GACCCCATTCTCTAC[-/A]AAAAAAAACACAGTA	10025
rs201876711	in-del	-/T			intron-variant	MED16	GRCh38.p7	19:879345	CCCCAGCAGCTCACC[-/T]TTCCCCTGGTTGTCA	10025
rs201895096	snp	A/C	0.0695416	0.173017	synonymous-codon, utr-variant-5-prime	MED16	GRCh38.p7	19:891102	CAAGTCCATCATCCC[A/C]CCTGCCGCTGGCCGC	10025
rs201908083	snp	A/G	0.00335642	0.0408282	intron-variant	MED16	GRCh38.p7	19:868269	GCAGGGCGGGCTGAG[A/G]TTAACCGCGCCGAGG	10025
rs201973018	snp	A/C	4.98865e-05	0.00499407	missense	MED16	GRCh38.p7	19:885831	GGAAACTTGTCCTTG[A/C]GGTTGAGGTCGGTGG	10025
rs202000331	snp	C/T	1.90758e-05	0.00308829	intron-variant	MED16	GRCh38.p7	19:871687	TAGCAGATATCAAGG[C/T]AGAGCCACTGCCACC	10025
rs202003208	snp	A/G	0.000141355	0.00840581	intron-variant	MED16	GRCh38.p7	19:881534	GAACTGAGGCCCCGC[A/G]TGGCTGCCGCTGGCT	10025
rs202050513	in-del	-/TGAGACAGAGTCTCACTCTGTC			intron-variant	MED16	GRCh38.p7	19:874131	CCTAAATTTTTTTTT[-/TGAGACAGAGTCTCACTCTGTC]GCCCAGGCTGGAGTG	10025
rs202086036	snp	A/G	1.69137e-05	0.00290802	missense	MED16	GRCh38.p7	19:872063	ATCAATTCCCGAAGC[A/G]TGCCCAGCGAGGTGC	10025
rs202109449	snp	A/C/G			intron-variant	MED16	GRCh38.p7	19:871877	GGGGAGCGGGGAGAG[A/C/G]GGAGAGCGGGGAGCG	10025
rs202122968	snp	A/C/T	6.78645e-05	0.00582474	missense	MED16	GRCh38.p7	19:872079	TGCCCAGCGAGGTGC[A/C/T]GTCCCGCAGAAAGCT	10025
rs202146478	in-del	-/CTT	0.0111196	0.0737302	intron-variant	MED16	GRCh38.p7	19:889108	CCCTGGCCACGCCTA[-/CTT]CTTAACTGTCCCCAA	10025
rs202162390	snp	C/G/T	0.000153797	0.008768	intron-variant	MED16	GRCh38.p7	19:868522	GAGGCAGGCACTGAG[C/G/T]GGGTTCCCACTTCCA	10025
rs202171261	snp	A/G	0.000206134	0.0101501	synonymous-codon	MED16	GRCh38.p7	19:868224	TCTGCTGGTCACGCA[A/G]GCGTCCGGCCCACGG	10025
rs202180804	snp	A/G	0.000476661	0.0154306	intron-variant	MED16	GRCh38.p7	19:890959	AGGTGGGAGGGGGAC[A/G]CACCCTGGTCATCGC	10025
rs202183179	snp	A/G			intron-variant	MED16	GRCh38.p7	19:878151	AATGCTCAGCAGCTC[A/G]CCTTCCCGTGGTTGT	10025
rs202206875	in-del	-/CACCAG			intron-variant	MED16	GRCh38.p7	19:877764	CTGGTTGTCAATGCC[-/CACCAG]CCCCAGCCCCAGCCC	10025
rs202246547	snp	C/T	3.65905e-05	0.00427714	intron-variant	MED16	GRCh38.p7	19:880192	GGGCAGGGCCCAGGA[C/T]ACGCCCGCCGGGGGA	10025
rs367549739	in-del	-/GCCCCAGCCCCACGT			intron-variant	MED16	GRCh38.p7	19:879763	TGTCAATGCCCACCA[-/GCCCCAGCCCCACGT]GCCCCAGCAGCTCGC	10025
rs367558987	snp	A/G			intron-variant	MED16	GRCh38.p7	19:877418	TGCACTGGATGCCGA[A/G]CCAGGCTTACACTCG	10025
rs367567945	snp	A/T			missense	MED16	GRCh38.p7	19:873468	TTGGGTAGGCTGGCC[A/T]GCAGGTACAGCACGA	10025
rs367577539	snp	A/G			intron-variant	MED16	GRCh38.p7	19:878806	CAGCCCCAGCCCCAC[A/G]TGCCCCAGCAGCTCC	10025
rs367603988	snp	A/G	3.43206e-05	0.00414236	intron-variant	MED16	GRCh38.p7	19:881732	GAAAAATCAGGGGCA[A/G]GAAAACAGGAAGGCA	10025
rs367611766	snp	A/G			intron-variant	MED16	GRCh38.p7	19:879399	ATGCCCCAGCAGCTC[A/G]CCTTTCCCTGGTTGT	10025
rs367646714	snp	C/T	0.000132406	0.00813546	intron-variant	MED16	GRCh38.p7	19:884857	AATAAAAACCAACCG[C/T]CCCCGAGGGCAGGCC	10025
rs367666846	snp	A/G	0.000141153	0.0083998	synonymous-codon	MED16	GRCh38.p7	19:871147	GCTAACCAGGCCGTC[A/G]CTGGCTGGCAGCCAG	10025
rs367670497	snp	A/C/G	6.09426e-05	0.00551981	intron-variant	MED16	GRCh38.p7	19:875485	CAGGTCACCCCAAGG[A/C/G]GCCGGAGCAGAGGCG	10025
rs367734322	snp	A/G	7.25347e-05	0.0060218	intron-variant	MED16	GRCh38.p7	19:880162	CCCTGTGGGGCACAG[A/G]CACTGCTTAGACATG	10025
rs367792516	snp	A/G	0.000176733	0.00939869	intron-variant	MED16	GRCh38.p7	19:880199	GCCCAGGACACGCCC[A/G]CCGGGGGAGGGGCCT	10025
rs367822902	snp	C/G			intron-variant	MED16	GRCh38.p7	19:887589	GAGAATCACTTGAAC[C/G]TGGGAGGTGGAAGTT	10025
rs367850686	snp	C/G			intron-variant	MED16	GRCh38.p7	19:883803	GCTGCAGGAGCCAGC[C/G]CAGCCCAAACTGCCT	10025
rs367851435	snp	C/T	0.000159987	0.00894249	missense	MED16	GRCh38.p7	19:871221	CATCCACCAGCGCCT[C/T]GTCCGGCTCGCTCGC	10025
rs367872121	snp	A/G	0.00159617	0.0282053	intron-variant	MED16	GRCh38.p7	19:871729	ATGTTCTGGCGGGGG[A/G]CTCAGGCAGGACTTG	10025
rs367957533	snp	C/T	0.00398564	0.0444627	downstream-variant-500B	MED16	GRCh38.p7	19:867946	GGTCGGGGGCACCGA[C/T]GGCAGGGACGCGGGC	10025
rs367962957	snp	C/G			intron-variant	MED16	GRCh38.p7	19:875609	AACCTCATGGCAAAA[C/G]AGGTGCGGAAGACCA	10025
rs367975481	snp	C/T			intron-variant	MED16	GRCh38.p7	19:881461	TCAGAGCCCACGTCC[C/T]CTGGTGTGAGCTCCC	10025
rs368002263	snp	A/C/G	0.0023933	0.0345097	intron-variant	MED16	GRCh38.p7	19:885556	CTGTGGCCACGAAGC[A/C/G]GGAGGAAGGCGCCCC	10025
rs368024977	snp	A/G			intron-variant	MED16	GRCh38.p7	19:878200	GCCCCACGTGCCCCA[A/G]CAGCTCACCTTCCCC	10025
rs368207547	snp	A/G			intron-variant	MED16	GRCh38.p7	19:871409	TTCTCTCACCAGGTC[A/G]GGGCCCCGGCTCTGC	10025
rs368220639	snp	C/T	1.67086e-05	0.00289033	synonymous-codon	MED16	GRCh38.p7	19:881674	ATCGTTGGTGGCCGA[C/T]AGGATCCGCCATTTG	10025
rs368229538	in-del	-/G			intron-variant	MED16	GRCh38.p7	19:871318	CGGCCACCCGGGACG[-/G]TGCTGGGAGCCCCTC	10025
rs368236739	in-del	-/G			intron-variant	MED16	GRCh38.p7	19:881488	CCCACGACCCCGTGG[-/G]CCTGTGCTCAGGGCC	10025
rs368247375	snp	A/C	1.86048e-05	0.00304993	intron-variant	MED16	GRCh38.p7	19:871628	TGGCTGCCATCCCAA[A/C]AGCACCCACACAGAG	10025
rs368248858	snp	C/G/T	0.000155988	0.00883005	synonymous-codon, missense	MED16	GRCh38.p7	19:880090	GAAGACGGCCATGGT[C/G/T]TGCAGTGAGAGCCGG	10025
rs368267705	snp	A/G	5.06556e-05	0.00503242	synonymous-codon, intron-variant	MED16	GRCh38.p7	19:889653	CTTCTCCACGTGCAG[A/G]GCCAGTTTCACACCA	10025
rs368293469	snp	C/T	0.000153988	0.00877328	missense	MED16	GRCh38.p7	19:875430	AGAGCGAGGCCTTCA[C/T]GGCCAGGATCCGGGT	10025
rs368370399	snp	C/T	6.71659e-05	0.00579469	synonymous-codon	MED16	GRCh38.p7	19:881695	CCGCCATTTGAGAAT[C/T]GTGGGCTGTTTGTCG	10025
rs368383193	snp	A/G/T	0.000502111	0.0158373	intron-variant	MED16	GRCh38.p7	19:868541	TTCCCACTTCCAGGC[A/G/T]GGCCTCCCTTACGCC	10025
rs368413375	snp	G/T			intron-variant	MED16	GRCh38.p7	19:887386	AAAAAACAAAAATTT[G/T]GCCGGACGCGGTGGC	10025
rs368414133	snp	C/T	1.68821e-05	0.0029053	missense, intron-variant	MED16	GRCh38.p7	19:889655	TCTCCACGTGCAGGG[C/T]CAGTTTCACACCATT	10025
rs368424152	snp	C/G	0.000261849	0.0114392	missense	MED16	GRCh38.p7	19:871187	GGGATAAGCAGCTGG[C/G]TGGGCAGCAGGCAGC	10025
rs368479273	snp	A/G	9.9935e-05	0.00706806	intron-variant	MED16	GRCh38.p7	19:868844	TCTCTGGGAGTCAGC[A/G]GTTCCGGGGGCCCCT	10025
rs368482672	snp	C/T	0.000343528	0.0131014	intron-variant	MED16	GRCh38.p7	19:875215	AGATGAAAGAAACCT[C/T]GAGGCCCCGGGCGTG	10025
rs368502301	snp	C/T	0.000218806	0.0104573	utr-variant-3-prime	MED16	GRCh38.p7	19:868095	GTCCGCCTGGACCCC[C/T]GGCCGTCACGGACGG	10025
rs368650017	snp	A/G			intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:891546	CCGAAGGAAGAGCCC[A/G]CAGACAGGCAAGCGG	10025
rs368658374	snp	C/T	0.00318978	0.0398085	intron-variant	MED16	GRCh38.p7	19:883708	GCTGTGGGCAGATGG[C/T]AGACACAGACGTGCC	10025
rs368706996	snp	A/C/G	0.000172743	0.00929229	intron-variant	MED16	GRCh38.p7	19:871588	ACAACCCGACAAGGA[A/C/G]AGACAGCAAACAGGT	10025
rs368724443	snp	A/G	0.0023933	0.0345097	intron-variant	MED16	GRCh38.p7	19:882756	TGAGCTGCTCAGTTT[A/G]GGGCTGGCTTGTTAC	10025
rs368736934	snp	A/G			intron-variant	MED16	GRCh38.p7	19:879427	TGTCAATGCCCACCA[A/G]CCCCAGCCCCACGTG	10025
rs368737553	snp	A/G/T	6.75901e-05	0.00581303	synonymous-codon, intron-variant	MED16	GRCh38.p7	19:877166	CATGGAAGGTGAGAG[A/G/T]CGGAGCACGCTCAGC	10025

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