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
rs368741567	snp	A/G			intron-variant	MED16	GRCh38.p7	19:878324	GCCCCACGTGCCCCA[A/G]CAGCTCACCTTCCCG	10025
rs368743271	snp	A/G	0.000159987	0.00894249	intron-variant	MED16	GRCh38.p7	19:890256	AGGTCTGTGGGGACG[A/G]GGCATGGTCAGCACG	10025
rs368744761	snp	A/G	0.00260586	0.0360019	missense	MED16	GRCh38.p7	19:871226	ACCAGCGCCTCGTCC[A/G]GCTCGCTCGCTGGGC	10025
rs368747520	snp	A/G			intron-variant	MED16	GRCh38.p7	19:882230	AAATGTGACATGGCC[A/G]GGCACAGCAGCTCAC	10025
rs368832060	snp	A/G			intron-variant	MED16	GRCh38.p7	19:880991	AGGGTTTTGGAGCAG[A/G]GAACTGCATCCCCTC	10025
rs368833200	snp	C/T			intron-variant	MED16	GRCh38.p7	19:869981	GTGACAAGGTCCCAC[C/T]TCACAGGGCTGCTGG	10025
rs368906339	snp	A/G			intron-variant	MED16	GRCh38.p7	19:874165	GTCGCCCAGGCTGGA[A/G]TGCAGTGGGGTGATC	10025
rs368953151	snp	A/G			intron-variant	MED16	GRCh38.p7	19:879774	ACCAGCCCCAGCCCC[A/G]CGTGCCCCAGCAGCT	10025
rs368953303	snp	C/T	6.99827e-05	0.00591493	intron-variant	MED16	GRCh38.p7	19:881542	GCCCCGCGTGGCTGC[C/T]GCTGGCTCCACCGTA	10025
rs369009728	snp	C/G	1.66985e-05	0.00288946	missense	MED16	GRCh38.p7	19:873523	GCTGCAGCGCCTGCA[C/G]TGTGTTCATGTCCAG	10025
rs369018479	snp	A/G	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:871901	GGGAGCGGGGAGAGG[A/G]GAGGGGCGGGCGGGG	10025
rs369042591	snp	C/G			intron-variant	MED16	GRCh38.p7	19:879231	AATGCCCACCAAGCC[C/G]AGCCCCACATGCCCC	10025
rs369054708	snp	A/C/G	0.000158856	0.00891095	synonymous-codon	MED16	GRCh38.p7	19:884958	TCCCTCCTTGCGCAG[A/C/G]GACCAGCACTCCACG	10025
rs369062233	snp	C/T	0.00117823	0.0242431	intron-variant	MED16	GRCh38.p7	19:868300	AGAGTCCAGGGCGAG[C/T]GGTGGCTCTTGCAGC	10025
rs369070095	snp	A/G			intron-variant	MED16	GRCh38.p7	19:888460	ACCCAGGAGGCAGAG[A/G]TTGCTGTGAGCCAAG	10025
rs369071813	snp	C/T	0.00199481	0.0315187	intron-variant	MED16	GRCh38.p7	19:884507	GGTTCCGGAGGATTC[C/T]GTGCACCGCCCCTGC	10025
rs369084724	snp	A/G	0.00159617	0.0282053	intron-variant	MED16	GRCh38.p7	19:884045	GCCCCGGGAGCCATC[A/G]GGGCCTCTTGACACG	10025
rs369102326	in-del	-/GCTCT	0.00146138	0.0269917	frameshift-variant	MED16	GRCh38.p7	19:868207	GGGGCTTCCTCAGAA[-/GCTCT]GCTGGTCACGCAGGC	10025
rs369178757	snp	C/T	0.000153988	0.00877328	intron-variant	MED16	GRCh38.p7	19:868411	GCCACCAGAGCCCAC[C/T]GCACAGGCAGTTCTT	10025
rs369228460	snp	A/G/T	0.000210023	0.0102458	intron-variant	MED16	GRCh38.p7	19:868967	GGGAGAGGGGAGAAC[A/G/T]TGAGGGAGGCCTGGG	10025
rs369230180	multinucleotide-polymorphism	AGA/GGG			intron-variant	MED16	GRCh38.p7	19:880560	CATTGTACGAGGGCC[AGA/GGG]GGGAGGTGGGGTCCA	10025
rs369231343	in-del	-/C	0.0437281	0.141251	intron-variant	MED16	GRCh38.p7	19:889175	CCCTGGCCACGCCTA[-/C]TCTTAACTGTCCCCC	10025
rs369232238	in-del	-/C/TTT			upstream-variant-2KB, nc-transcript-variant	MED16, RNU6-9	GRCh38.p7	19:893586	GTGAAGCGTTCCATA[-/C/TTT]TTTTTTTTTTTTCCA	10025
rs369283862	in-del	-/AAAC			intron-variant	MED16	GRCh38.p7	19:888207	AGACCCTGTCTCAAA[-/AAAC]AAACAAACAAACAAA	10025
rs369309247	snp	C/G			intron-variant	MED16	GRCh38.p7	19:886591	GCTGGTGCCAATGAG[C/G]CACACTCACAAACCC	10025
rs369311520	snp	A/G			intron-variant	MED16	GRCh38.p7	19:878928	ACCAGCCCCGGCCCC[A/G]GCCCCGGCCCCGGCC	10025
rs369339727	snp	A/G	0.00242206	0.0347155	synonymous-codon, intron-variant	MED16	GRCh38.p7	19:889647	ACTCACCTTCTCCAC[A/G]TGCAGGGCCAGTTTC	10025
rs369340119	snp	C/G	1.66983e-05	0.00288944	synonymous-codon	MED16	GRCh38.p7	19:885800	CCGGGCCAGGAACTT[C/G]AGGTGGGTGATGGCG	10025
rs369347363	snp	C/G	3.58944e-05	0.00423626	intron-variant	MED16	GRCh38.p7	19:877213	CAAGGAGAGCCCGGT[C/G]AGATGGGGCTGCGCC	10025
rs369358220	snp	A/G	0.000156869	0.00885493	intron-variant	MED16	GRCh38.p7	19:884892	GCCTCCGCAGCCGGC[A/G]GGAGACTCACCCACG	10025
rs369426295	snp	A/C/T	0.000101698	0.00713024	intron-variant	MED16	GRCh38.p7	19:868277	GGCTGAGGTTAACCG[A/C/T]GCCGAGGAGAGTCCA	10025
rs369438282	snp	A/G	0.00295335	0.0383139	synonymous-codon	MED16	GRCh38.p7	19:871996	ATCCGAGGTGGCCGT[A/G]TACACGGGCAGGCAG	10025
rs369450591	snp	C/T	3.5548e-05	0.00421577	intron-variant	MED16	GRCh38.p7	19:881530	GTGTGAACTGAGGCC[C/T]CGCGTGGCTGCCGCT	10025
rs369452653	snp	A/G	1.7912e-05	0.0029926	intron-variant	MED16	GRCh38.p7	19:868409	CCGCCACCAGAGCCC[A/G]CCGCACAGGCAGTTC	10025
rs369567178	snp	A/G	0.000778664	0.0197161	intron-variant	MED16	GRCh38.p7	19:884883	AGGCCCAGGGCCTCC[A/G]CAGCCGGCGGGAGAC	10025
rs369568636	snp	A/G	0.000164958	0.00908028	utr-variant-3-prime	MED16	GRCh38.p7	19:868084	GTCACCACAAGGTCC[A/G]CCTGGACCCCCGGCC	10025
rs369569324	snp	A/G	0.00279162	0.0372561	intron-variant	MED16	GRCh38.p7	19:884172	CCTGTGCTCTCATCT[A/G]CCGGGAAAACATCTC	10025
rs369580975	snp	C/T	6.08439e-05	0.00551527	intron-variant	MED16	GRCh38.p7	19:872150	TCGGTGTGGCTGGGG[C/T]GGCGGGGGGCAGATG	10025
rs369584567	snp	A/G	0.000264122	0.0114888	intron-variant	MED16	GRCh38.p7	19:868261	ACAGCCCTGCAGGGC[A/G]GGCTGAGGTTAACCG	10025
rs369597753	snp	C/T			intron-variant	MED16	GRCh38.p7	19:879174	AGCAGCTCGCCTTCC[C/T]CTGGTTGTCAATGCC	10025
rs369632896	snp	A/G	0.000161987	0.00899817	synonymous-codon	MED16	GRCh38.p7	19:871249	CGCTGGGCCCTCATC[A/G]CGACCTGCGGAGAGA	10025
rs369688868	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:869125	CCTGAGACAGGCCCA[A/G]TAAAGGGGGCGGGAC	10025
rs369767102	snp	A/C	0.0001036	0.00719648	intron-variant	MED16	GRCh38.p7	19:890134	GTGGGACCAGCGCCT[A/C]ACCTGACTGGTCCCA	10025
rs369785586	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:883280	AGAGCTGGGCATGGC[A/G]GGGACCGAAGCCTGG	10025
rs369801220	snp	C/T	5.40117e-05	0.00519644	intron-variant	MED16	GRCh38.p7	19:877191	CTCAGCTGCCAGAGA[C/T]AGAGCCCAAGGAGAG	10025
rs369907792	snp	A/G			intron-variant	MED16	GRCh38.p7	19:884343	GGGGATGACGGGCTT[A/G]GCTCCGTGGGTGCGG	10025
rs369931110	snp	A/G	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:868776	CCACCACCCTTGACC[A/G]TCTGGAGCGCTGGGT	10025
rs369941648	snp	A/G	0.00676609	0.0577691	intron-variant	MED16	GRCh38.p7	19:876404	TTGCTGAGGCCTCAC[A/G]CCACAGGGCCACCGG	10025
rs369984322	snp	A/G	0.000139003	0.00833561	missense	MED16	GRCh38.p7	19:886101	ACCAGGCCGCTGACC[A/G]TCACCGCGATCCAGC	10025
rs369998338	snp	A/G			intron-variant	MED16	GRCh38.p7	19:879675	TGTCAATGCCCACCA[A/G]CCCCAGCCCCACGTG	10025
rs370061734	snp	A/T	3.87207e-05	0.00439987	intron-variant	MED16	GRCh38.p7	19:871581	CATACACACAACCCG[A/T]CAAGGAGAGACAGCA	10025
rs370068240	snp	C/T	6.02452e-05	0.00548808	missense	MED16	GRCh38.p7	19:886081	GCTTCAGCAGGGACA[C/T]GGTGACCAGGCCGCT	10025
rs370073131	snp	C/T	0.000189982	0.00974448	missense	MED16	GRCh38.p7	19:871050	ACCTGGCGAGGCCGT[C/T]GAGCTGCAGGGTGGC	10025
rs370135829	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:877236	GCTGCGCCCTCAGCC[A/G]GGAGAGGAATGGGGC	10025
rs370140209	snp	A/G			intron-variant	MED16	GRCh38.p7	19:884387	CGGATAGAGATGGGA[A/G]TGGGGGCCCCAGAAG	10025
rs370156729	snp	G/T	2.52701e-05	0.00355449	intron-variant	MED16	GRCh38.p7	19:875473	AGGGCAGGAAGCCAG[G/T]TCACCCCAAGGGGCC	10025
rs370170141	snp	C/G			upstream-variant-2KB, downstream-variant-500B	MED16, RNU6-9	GRCh38.p7	19:893632	AAACGGAATCTTGCT[C/G]TGTTGCCCAGGCTGG	10025
rs370198546	snp	A/G			intron-variant	MED16	GRCh38.p7	19:878522	GCCCCACGTGCCCCA[A/G]CAGCTCACCTTCCCG	10025
rs370208041	snp	C/T			intron-variant	MED16	GRCh38.p7	19:878172	CCGTGGTTGTCAATG[C/T]CCACCGAGCCCAGCC	10025
rs370210812	snp	A/G	0.000187045	0.0096689	synonymous-codon	MED16	GRCh38.p7	19:868134	ATGCAGATGGTCCAG[A/G]GATCTGGGGGTCCTG	10025
rs370211321	in-del	-/GC			intron-variant	MED16	GRCh38.p7	19:871774	AGGGGAGCGGGGAGA[-/GC]GGGGAGAGGGGAGAG	10025
rs370213588	snp	A/G			intron-variant	MED16	GRCh38.p7	19:881394	TCTGCCTCCTAATTG[A/G]GAACCCATCAGAACC	10025
rs370229226	snp	C/T			intron-variant	MED16	GRCh38.p7	19:878579	CCCCAGCCCCACATG[C/T]CCCAGCAGCTCACCT	10025
rs370231262	snp	G/T			intron-variant	MED16	GRCh38.p7	19:869477	CTCTCATTAAATATC[G/T]GAAATTTTCCCAGTT	10025
rs370231731	snp	A/G/T	0.000208475	0.0102077	intron-variant	MED16	GRCh38.p7	19:871678	CTGGGGAAATAGCAG[A/G/T]TATCAAGGCAGAGCC	10025
rs370236147	snp	C/T	1.87064e-05	0.00305825	intron-variant	MED16	GRCh38.p7	19:889601	GGTAGGGTGACATCT[C/T]ATCTGCCTCATCCGC	10025
rs370258960	snp	C/T			intron-variant	MED16	GRCh38.p7	19:885387	GACCGGTGGCTGGGC[C/T]GCCTCTCACAGAGAA	10025
rs370259999	snp	C/G	0.000153988	0.00877327	intron-variant	MED16	GRCh38.p7	19:873438	GGGCCTTAGGGGAGA[C/G]CATGGCGCACCTGGT	10025
rs370268245	snp	A/G	0.000229419	0.0107078	intron-variant	MED16	GRCh38.p7	19:885060	TGCTGTGGTGGCCAC[A/G]CCACCACCGGAGCCT	10025
rs370307890	snp	C/T			missense	MED16	GRCh38.p7	19:871071	GCAGGGTGGCAGCAC[C/T]GCCAGGCAGCGTGGG	10025
rs370321826	snp	G/T			intron-variant	MED16	GRCh38.p7	19:884815	GTTCAGGACCACCCT[G/T]GGTGACACAGCAAGA	10025
rs370338394	snp	A/C	0.00398564	0.0444627	intron-variant	MED16	GRCh38.p7	19:877424	GGATGCCGAGCCAGG[A/C]TTACACTCGTCTGCT	10025
rs370344539	snp	C/T	0.00338968	0.0410287	intron-variant	MED16	GRCh38.p7	19:880198	GGCCCAGGACACGCC[C/T]GCCGGGGGAGGGGCC	10025
rs370369782	snp	C/G			upstream-variant-2KB, downstream-variant-500B	MED16, RNU6-9	GRCh38.p7	19:894026	GCAATGGATGTGGTG[C/G]TCTTCTATTTTTATT	10025
rs370404490	snp	C/T			intron-variant	MED16	GRCh38.p7	19:870180	CAGAGGGATCTACGG[C/T]GAGGCCTGACATCCA	10025
rs370416561	snp	C/G			intron-variant	MED16	GRCh38.p7	19:872698	TCAGGGGCGCACAAG[C/G]CGCAGAACTGAAGGT	10025
rs370470379	snp	C/G			utr-variant-3-prime	MED16	GRCh38.p7	19:867965	AGGGACGCGGGCCTG[C/G]GCGCAGAGGGCGTTT	10025
rs370477649	snp	A/C			splice-acceptor-variant	MED16	GRCh38.p7	19:881715	GCTGTTTGTCGCCAA[A/C]TGAAAAATCAGGGGC	10025
rs370493746	snp	C/G/T	0.000100042	0.00707193	synonymous-codon	MED16	GRCh38.p7	19:875302	GGGGCTCTTGTCAGG[C/G/T]GTGTTGAGAAAGTGG	10025
rs370546409	in-del	-/G			intron-variant	MED16	GRCh38.p7	19:885454	GCACGTTGGGGGGGG[-/G]TCCGGGGGCCCCAGT	10025
rs370563314	snp	A/G	0.000686224	0.0185106	intron-variant	MED16	GRCh38.p7	19:871258	CTCATCGCGACCTGC[A/G]GAGAGAGGTGGCGGA	10025
rs370567757	snp	C/G			intron-variant	MED16	GRCh38.p7	19:879316	GTCAATGCCCACCAA[C/G]CCCAGCCCCACGTGC	10025
rs370577388	snp	A/G	0.000148971	0.00862921	synonymous-codon, utr-variant-5-prime	MED16	GRCh38.p7	19:891090	ACAGACGTAGGCCAA[A/G]TCCATCATCCCACCT	10025
rs370621279	snp	A/C/T	0.000191319	0.00977903	synonymous-codon, intron-variant	MED16	GRCh38.p7	19:877142	CAGCCCCACCTCCAG[A/C/T]GGGTGGCCCATGGAA	10025
rs370700407	snp	C/G	1.68772e-05	0.00290488	missense	MED16	GRCh38.p7	19:868466	CACCGCCGTGGTTCT[C/G]TTGGGCGACTTGAGC	10025
rs370725536	snp	A/G	0.000101545	0.00712477	synonymous-codon	MED16	GRCh38.p7	19:868496	CATGGTGACACAGCC[A/G]CACCTGCGGGGAGGC	10025
rs370804977	snp	A/G	0.000114688	0.0075717	intron-variant	MED16	GRCh38.p7	19:871594	CGACAAGGAGAGACA[A/G]CAAACAGGTGCCTGG	10025
rs370810616	in-del	-/TT	0.317692	0.240661	upstream-variant-2KB, nc-transcript-variant	MED16, RNU6-9	GRCh38.p7	19:893586	GTGAAGCGTTCCATA[-/TT]TTTTTTTTTTTTTCC	10025
rs370817085	snp	C/T	0.00517822	0.0506191	downstream-variant-500B	MED16	GRCh38.p7	19:867678	GAGATACCAGAGACA[C/T]GCAGAAACAAGGAGA	10025
rs370863921	snp	C/T	0.000153988	0.00877328	intron-variant	MED16	GRCh38.p7	19:873622	AGCTCGGGCCTCTTG[C/T]ACACACAGGGTGACC	10025
rs370902120	snp	C/G			downstream-variant-500B	MED16	GRCh38.p7	19:867499	AGGCCTGCTGGAGAC[C/G]GAAGGCGGGACCCCT	10025
rs370908929	snp	C/T			intron-variant	MED16	GRCh38.p7	19:878219	CTCACCTTCCCCTGG[C/T]TGTCAATGCCCACCA	10025
rs370975859	snp	A/G/T	7.6037e-05	0.00616544	intron-variant	MED16	GRCh38.p7	19:885020	GCACCTGCGGGGGAG[A/G/T]TGGGGGTGAGGGCTG	10025
rs370992115	snp	A/G			intron-variant	MED16	GRCh38.p7	19:881259	GAGAGGACACATGCC[A/G]CCTACCCAGGAAGGA	10025
rs371063978	snp	A/G			intron-variant	MED16	GRCh38.p7	19:879847	GTGCCCCAGCAGCTC[A/G]CCTTCCCCTGGTTGT	10025
rs371095210	snp	A/C	1.70499e-05	0.0029197	intron-variant	MED16	GRCh38.p7	19:868517	GCGGGGAGGCAGGCA[A/C]TGAGCGGGTTCCCAC	10025
rs371104390	snp	C/T	0.000289571	0.0120292	intron-variant	MED16	GRCh38.p7	19:875488	GTCACCCCAAGGGGC[C/T]GGAGCAGAGGCGCCC	10025
rs371111559	snp	C/T	0.000281413	0.0118586	missense	MED16	GRCh38.p7	19:871149	TAACCAGGCCGTCGC[C/T]GGCTGGCAGCCAGTC	10025
rs371135411	snp	A/G	0.00436764	0.0465268	intron-variant	MED16	GRCh38.p7	19:885040	GGTGAGGGCTGACCC[A/G]GCACTGCTGTGGTGG	10025
rs371353391	snp	C/G			intron-variant	MED16	GRCh38.p7	19:878339	GCAGCTCACCTTCCC[C/G]TGGTTGTCAATGCCC	10025
rs371356240	snp	A/T			intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:892111	GCACCTCCTCGAGGC[A/T]TTCTAAGCGCCTGGC	10025
rs371405209	snp	C/T	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:877315	GTGGGCCTGTGTGCG[C/T]GCATGTGTCTGTAGC	10025
rs371415029	snp	A/G	1.93898e-05	0.0031136	missense	MED16	GRCh38.p7	19:880034	GTGCGGGGGCGCTTC[A/G]TGGCCGGCTCATCCA	10025
rs371464457	snp	A/C	0.000153988	0.00877327	missense, intron-variant	MED16	GRCh38.p7	19:877026	TGCAGCTTCTCCACC[A/C]GGCTCTGTACCATAC	10025
rs371473900	snp	C/T	0.000535537	0.0163549	intron-variant	MED16	GRCh38.p7	19:880194	GCAGGGCCCAGGACA[C/T]GCCCGCCGGGGGAGG	10025
rs371499870	snp	A/C/T	0.000155988	0.00883004	missense	MED16	GRCh38.p7	19:880008	CCTTTAAGTGGACGG[A/C/T]GGGGCCCGCGGTGCG	10025
rs371520838	snp	C/T			intron-variant	MED16	GRCh38.p7	19:876680	GCCCTCCGCCTGCCA[C/T]AGAGCCCCCAACCTG	10025
rs371557917	snp	C/T			intron-variant	MED16	GRCh38.p7	19:870887	GGATTCGGGGGGTCC[C/T]GGGCAGGACATGGAG	10025
rs371563432	snp	A/G			intron-variant	MED16	GRCh38.p7	19:870507	CAGACGTTGCAGTGG[A/G]CCAAGACGGCACTAC	10025
rs371567287	in-del	-/AG			intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:891745	GCGGGGCTGACTGAC[-/AG]GGAACACCTGTGGCC	10025
rs371608256	snp	A/C	2.37917e-05	0.00344895	missense	MED16	GRCh38.p7	19:871933	TGCCTCACAGCAGAT[A/C]CAGAGCTTGGTGAGC	10025
rs371649201	snp	C/T			intron-variant	MED16	GRCh38.p7	19:879404	CCAGCAGCTCACCTT[C/T]CCCTGGTTGTCAATG	10025
rs371786864	snp	A/C	0.000225261	0.0106104	intron-variant	MED16	GRCh38.p7	19:884887	CCAGGGCCTCCGCAG[A/C]CGGCGGGAGACTCAC	10025
rs371787399	snp	C/T	0.000188679	0.00971103	synonymous-codon	MED16	GRCh38.p7	19:868886	GGCCTTGCATTCCTC[C/T]GTGGGGCAAGCGCCA	10025
rs371802904	snp	A/G	0.000283435	0.0119011	intron-variant	MED16	GRCh38.p7	19:872151	CGGTGTGGCTGGGGC[A/G]GCGGGGGGCAGATGG	10025
rs371880839	snp	A/C/G/T	0.00301915	0.0387514	intron-variant	MED16	GRCh38.p7	19:876967	CCCACCTGCCACGGG[A/C/G/T]CCCCACCTGCTGCAG	10025
rs371883148	snp	A/C			intron-variant	MED16	GRCh38.p7	19:887421	GCCTGTAATCTCAGC[A/C]CTTTGGGAGGCCGAG	10025
rs371912127	snp	A/C/G	1.71982e-05	0.00293237	intron-variant	MED16	GRCh38.p7	19:890953	GGAAGCAGGTGGGAG[A/C/G]GGGACGCACCCTGGT	10025
rs371939662	snp	A/T			intron-variant	MED16	GRCh38.p7	19:877718	ATGCCCACCAGCCCC[A/T]GCCCCACGTGCCCCA	10025
rs371965593	snp	C/T			intron-variant	MED16	GRCh38.p7	19:878315	CCAGCCCCAGCCCCA[C/T]GTGCCCCAGCAGCTC	10025
rs371971471	snp	A/G/T			intron-variant	MED16	GRCh38.p7	19:881980	CACCATCTCACCCCC[A/G/T]ATGGGGCAGACAGTG	10025
rs372016928	snp	C/G	0.000163987	0.00905353	intron-variant	MED16	GRCh38.p7	19:890125	CCTGGCCACGTGGGA[C/G]CAGCGCCTCACCTGA	10025
rs372038736	snp	A/G			intron-variant	MED16	GRCh38.p7	19:888613	CGAAACCTCTGGACC[A/G]TGTGGGCTGCACACT	10025
rs372058557	snp	A/C/G			intron-variant	MED16	GRCh38.p7	19:879599	GCAGCTCACCTTCCC[A/C/G]TGGTTGTCAATGCCC	10025
rs372078714	snp	C/T			intron-variant	MED16	GRCh38.p7	19:877830	GCCTTCCCGTGGTTG[C/T]CAATGCCCACCAAGC	10025
rs372151569	snp	C/G/T	0.000130386	0.00807332	intron-variant	MED16	GRCh38.p7	19:871646	CACCCACACAGAGCA[C/G/T]GGACCTGTGCTAGGA	10025
rs372187260	snp	C/G	1.89206e-05	0.0030757	synonymous-codon	MED16	GRCh38.p7	19:875440	CTTCATGGCCAGGAT[C/G]CGGGTGGAGAGGACC	10025
rs372200845	snp	G/T			intron-variant	MED16	GRCh38.p7	19:883150	TTCCTAAATGAGGGG[G/T]GACTTGAGGCAGGGA	10025
rs372210642	snp	C/T	0.00358779	0.0422022	intron-variant	MED16	GRCh38.p7	19:885665	GCCCTGCCCACACCA[C/T]GGTTTAGCCCGTGGA	10025
rs372212477	snp	C/T			intron-variant	MED16	GRCh38.p7	19:875671	TGGGAGCGGCTCTGC[C/T]TCTGGTGGGGGCCCC	10025
rs372215882	snp	A/C/T	8.70411e-05	0.00659651	intron-variant	MED16	GRCh38.p7	19:875227	CCTCGAGGCCCCGGG[A/C/T]GTGGAAAAGGACCCA	10025
rs372224598	in-del	-/A	0.000731358	0.0191087	intron-variant	MED16	GRCh38.p7	19:876929	GCCCCCACCTGCCAC[-/A]GGGCCCCCACCTGCC	10025
rs372252782	snp	A/G	7.73739e-05	0.0062194	missense	MED16	GRCh38.p7	19:868154	TGGGGGTCCTGGGAG[A/G]GTGGTGTGTGGACTG	10025
rs372262696	snp	A/G	9.50543e-05	0.00689334	intron-variant	MED16	GRCh38.p7	19:871683	GAAATAGCAGATATC[A/G]AGGCAGAGCCACTGC	10025
rs372311899	snp	A/C/G	0.000406771	0.0142558	missense	MED16	GRCh38.p7	19:868238	AGGCGTCCGGCCCAC[A/C/G]GCCTTCAACAGCCCT	10025
rs372337956	snp	A/C	1.71655e-05	0.00292958	intron-variant	MED16	GRCh38.p7	19:881734	AAAATCAGGGGCAGG[A/C]AAACAGGAAGGCAAT	10025
rs372367009	snp	A/C/T	0.000169566	0.00920621	synonymous-codon	MED16	GRCh38.p7	19:885941	GAACTGCACGGGCGA[A/C/T]GCGCTGCTGCCGTCC	10025
rs372372589	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	MED16	GRCh38.p7	19:894393	CCAGGCTGATTTCAA[A/G]CTCCAGGCCTCAAGC	10025
rs372378240	snp	A/G	0.00438332	0.0466095	intron-variant	MED16	GRCh38.p7	19:869856	GGCTGGGGGTCTGAC[A/G]GGCCTGGGTTCAAAT	10025
rs372383079	snp	A/G	0.000126326	0.00794652	intron-variant	MED16	GRCh38.p7	19:884862	AAACCAACCGCCCCC[A/G]AGGGCAGGCCCAGGG	10025
rs372425188	snp	A/G			intron-variant	MED16	GRCh38.p7	19:884095	AGGAGCGCCTGCCCC[A/G]CCTGCCCCACGTGCC	10025
rs372436235	snp	G/T			intron-variant	MED16	GRCh38.p7	19:873282	GGGCTGAGGTGGGAC[G/T]CCAAGCAGGGGCGGG	10025
rs372449928	snp	C/T			intron-variant	MED16	GRCh38.p7	19:889312	AGCAGCCACCAGTTA[C/T]ACATGCAGCTACCTA	10025
rs372467140	snp	A/G			intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:892465	AGACTCCACCCCGGG[A/G]ACCCCACGTACTCTC	10025
rs372479505	snp	A/G			intron-variant	MED16	GRCh38.p7	19:868785	TTGACCGTCTGGAGC[A/G]CTGGGTGGGGGCTAG	10025
rs372488846	snp	G/T			intron-variant	MED16	GRCh38.p7	19:876476	AGAAAGATACCTCCA[G/T]ACTGGGAACACTGGA	10025
rs372496054	snp	A/G			intron-variant	MED16	GRCh38.p7	19:879688	CAGCCCCAGCCCCAC[A/G]TGCCCCAGCAGCTCG	10025
rs372502487	snp	C/T	0.00517822	0.0506191	intron-variant	MED16	GRCh38.p7	19:875929	AGAGCCTGTGCAACG[C/T]AGGACACCCCATCTC	10025
rs372527784	snp	A/G	0.000240819	0.0109705	intron-variant	MED16	GRCh38.p7	19:890327	GCAGGCTCCAGGTAA[A/G]CCGGTGTGTGTCCCA	10025
rs372546200	snp	A/G	0.000169133	0.00919445	synonymous-codon, utr-variant-5-prime	MED16	GRCh38.p7	19:886184	GGAGAACTTCTCCCC[A/G]AAGCTGGAGGCGCCC	10025
rs372579061	in-del	-/GCCCCAGCCCCACGT			intron-variant	MED16	GRCh38.p7	19:878501	TGTCAATGCCCACCA[-/GCCCCAGCCCCACGT]GCCCCAGCAGCTCAC	10025
rs372588007	snp	A/G			intron-variant	MED16	GRCh38.p7	19:881147	CCACATTTTACAGCT[A/G]AGCAAATAGGGTAGG	10025
rs372596844	snp	C/G			intron-variant	MED16	GRCh38.p7	19:878537	GCAGCTCACCTTCCC[C/G]TGGTTGTCAATGCCC	10025
rs372597457	snp	C/T			intron-variant	MED16	GRCh38.p7	19:879262	AGCAGCTCGCCTTCC[C/T]CTGGTTGTCAATGCC	10025
rs372613097	snp	C/T	1.68301e-05	0.00290082	synonymous-codon	MED16	GRCh38.p7	19:885776	CCCGTTCACCTGCTC[C/T]GACATGTCCCGGGCC	10025
rs372660299	snp	A/G	0.00279162	0.0372561	intron-variant	MED16	GRCh38.p7	19:886347	TCGGCCACCTGAGCC[A/G]TGTGGGATGTGATCC	10025
rs372664627	snp	A/T			intron-variant	MED16	GRCh38.p7	19:870403	GCCTCTATACCAAAA[A/T]TACAAAAAATACCTA	10025
rs372723333	snp	A/G	0.000872296	0.0208659	intron-variant	MED16	GRCh38.p7	19:881543	CCCCGCGTGGCTGCC[A/G]CTGGCTCCACCGTAC	10025
rs372729340	snp	G/T			missense	MED16	GRCh38.p7	19:872049	TGCGGATGACCACCA[G/T]CAATTCCCGAAGCAT	10025
rs372756465	snp	C/G/T	7.14023e-05	0.00597468	intron-variant	MED16	GRCh38.p7	19:881522	CTCCCCTGGTGTGAA[C/G/T]TGAGGCCCCGCGTGG	10025
rs372778012	snp	A/G	0.000602811	0.0173506	utr-variant-3-prime	MED16	GRCh38.p7	19:868088	CCACAAGGTCCGCCT[A/G]GACCCCCGGCCGTCA	10025
rs372788895	snp	G/T	0.000298274	0.0122085	intron-variant	MED16	GRCh38.p7	19:877215	AGGAGAGCCCGGTGA[G/T]ATGGGGCTGCGCCCT	10025
rs372822683	snp	A/G	0.00014555	0.00852958	intron-variant	MED16	GRCh38.p7	19:890271	GGGCATGGTCAGCAC[A/G]GCCTGGCACCACAGC	10025
rs372827473	snp	A/T	0.000267711	0.0115665	intron-variant	MED16	GRCh38.p7	19:873411	ATGAGATGGGGGCCC[A/T]GGTGGGGGGCGGGGC	10025
rs372842343	snp	C/T	0.000275734	0.0117384	intron-variant	MED16	GRCh38.p7	19:881554	TGCCGCTGGCTCCAC[C/T]GTACCGAGGCCAGGG	10025
rs372870789	snp	A/C/G	0.00023606	0.0108619	intron-variant	MED16	GRCh38.p7	19:872123	AGCAGGGAACCCTGC[A/C/G]CGAAAGAGGCATCGG	10025
rs372892063	snp	C/T	7.09031e-05	0.0059537	intron-variant	MED16	GRCh38.p7	19:881533	TGAACTGAGGCCCCG[C/T]GTGGCTGCCGCTGGC	10025
rs372897486	snp	A/G	5.93366e-05	0.00544654	intron-variant	MED16	GRCh38.p7	19:886222	GAGAAGGGAGGGAGG[A/G]AGGAGGGGCCGCTCA	10025
rs372897820	snp	A/C/G/T	0.00110054	0.023436	intron-variant	MED16	GRCh38.p7	19:871710	CTGCCACCTGCAGGG[A/C/G/T]CTTATGTTCTGGCGG	10025
rs372917971	snp	A/G	0.000181983	0.00953723	synonymous-codon	MED16	GRCh38.p7	19:871093	CAGCGTGGGCGCCCG[A/G]CCAAACTGCAGACGA	10025
rs372929744	snp	C/G			intron-variant	MED16	GRCh38.p7	19:878773	GCAGCTCCCCTTCCC[C/G]TGGTTGTCAATGCCC	10025
rs372942262	snp	A/C/G	0.0115144	0.0749975	intron-variant	MED16	GRCh38.p7	19:871903	GAGCGGGGAGAGGGG[A/C/G]GGGGCGGGCGGGGGT	10025
rs373031828	snp	A/C/G/T	0.000342069	0.0130743	intron-variant	MED16	GRCh38.p7	19:868988	GAGGCCTGGGCACCA[A/C/G/T]GAGGCCAGGTTCCGG	10025
rs373048886	snp	G/T			intron-variant	MED16	GRCh38.p7	19:872650	AGGACAGAGTGTACC[G/T]GCGGGGGGGTGGGGG	10025
rs373081824	snp	C/G			intron-variant	MED16	GRCh38.p7	19:883319	GCACGTGGGGCGGTG[C/G]GTGAAGAGCTGGGCA	10025
rs373113340	snp	A/G			intron-variant	MED16	GRCh38.p7	19:871305	ACTGGGGCACCGCCC[A/G]GCCACCCGGGACGTG	10025
rs373227893	snp	A/G			intron-variant	MED16	GRCh38.p7	19:878458	CGGCCCCGGCCCCAC[A/G]TGCCCCAGCAGCTCA	10025
rs373228669	snp	C/G	0.0040771	0.0449658	intron-variant	MED16	GRCh38.p7	19:879899	CCCCTGGTTGTCAAT[C/G]CCCACCAGCCCCGGC	10025
rs373231355	snp	C/T			intron-variant	MED16	GRCh38.p7	19:869001	CACGAGGCCAGGTTC[C/T]GGCAGGGGCATCTGT	10025
rs373300994	snp	A/G			intron-variant	MED16	GRCh38.p7	19:869370	GCCTGGAGGTGCCGG[A/G]ACCTCTGAACGACAA	10025
rs373308433	snp	A/G	0.0023933	0.0345097	intron-variant	MED16	GRCh38.p7	19:884349	GACGGGCTTGGCTCC[A/G]TGGGTGCGGGGGGCC	10025
rs373315881	snp	C/T	0.000136337	0.0082553	intron-variant	MED16	GRCh38.p7	19:884898	GCAGCCGGCGGGAGA[C/T]TCACCCACGGGGGAG	10025
rs373461561	snp	A/C	0.000102499	0.00715815	intron-variant	MED16	GRCh38.p7	19:885012	GCACAAAAGCACCTG[A/C]GGGGGAGGTGGGGGT	10025
rs373485164	snp	A/G	0.000263817	0.0114821	missense	MED16	GRCh38.p7	19:871227	CCAGCGCCTCGTCCG[A/G]CTCGCTCGCTGGGCC	10025
rs373503269	snp	C/T	0.000325947	0.0127619	missense	MED16	GRCh38.p7	19:871250	GCTGGGCCCTCATCG[C/T]GACCTGCGGAGAGAG	10025
rs373507537	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:880997	TTGGAGCAGGGAACT[A/G]CATCCCCTCAACCTC	10025
rs373527214	in-del	-/CAAT	0.0429648	0.14013	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:891506	GAGTGATGATGGGGG[-/CAAT]CAGCAAGTGGACACT	10025
rs373548105	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:887141	AAAATGCGAGGAAGA[A/G]AAGTGTATCATACGT	10025
rs373618894	snp	A/C/G	0.00279162	0.0372561	intron-variant	MED16	GRCh38.p7	19:881205	GGGCACGGATGCCAC[A/C/G]GTTTGAGCTCAGGAC	10025
rs373632661	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:872258	GTCAGGACTGGGGTG[C/T]TTCTGGCACCGAGTG	10025
rs373688060	snp	A/C/G	5.41466e-05	0.00520296	intron-variant	MED16	GRCh38.p7	19:889615	TCATCTGCCTCATCC[A/C/G]CTCACTCGGGCAGGA	10025
rs373709161	snp	C/T	8.23384e-05	0.0064158	intron-variant	MED16	GRCh38.p7	19:877222	CCCGGTGAGATGGGG[C/T]TGCGCCCTCAGCCGG	10025
rs373741447	in-del	-/CACT			intron-variant	MED16	GRCh38.p7	19:889359	GTGAAAGAGATAACT[-/CACT]AAGAACGGCCACCCT	10025
rs373765974	snp	A/G	0.000681245	0.0184434	missense	MED16	GRCh38.p7	19:871092	GCAGCGTGGGCGCCC[A/G]GCCAAACTGCAGACG	10025
rs373808985	snp	C/G	5.90755e-05	0.00543454	missense	MED16	GRCh38.p7	19:868225	CTGCTGGTCACGCAG[C/G]CGTCCGGCCCACGGC	10025
rs373850613	snp	A/T	1.82045e-05	0.00301694	intron-variant	MED16	GRCh38.p7	19:889612	ATCTCATCTGCCTCA[A/T]CCGCTCACTCGGGCA	10025
rs373862181	snp	A/G	0.000531334	0.0162906	intron-variant	MED16	GRCh38.p7	19:875484	CCAGGTCACCCCAAG[A/G]GGCCGGAGCAGAGGC	10025
rs373909448	in-del	-/CCAGCC			intron-variant	MED16	GRCh38.p7	19:878020	GGTTGTCAACGCCCA[-/CCAGCC]CCAGCCCCAGCCCCA	10025
rs373970382	snp	C/T	0.00358779	0.0422022	intron-variant	MED16	GRCh38.p7	19:891410	GGGTTTCACCAGGAC[C/T]CCTCTGGCTGTCTAG	10025
rs373987834	snp	C/T			intron-variant	MED16	GRCh38.p7	19:881947	GGCCCTGGGATTTCA[C/T]GGAAACCTGTGGGCC	10025
rs373989880	snp	C/G			intron-variant	MED16	GRCh38.p7	19:878227	CCCCTGGTTGTCAAT[C/G]CCCACCAGCCCCAGC	10025
rs374001986	snp	C/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:881108	AGCTGGGGGAAGAAA[C/G]GGCCTGAGCTAGGGC	10025
rs374041857	snp	C/T			intron-variant	MED16	GRCh38.p7	19:870660	GACACCACTAGGGGA[C/T]GGAGTTAGGGGCACC	10025
rs374083426	snp	A/G			intron-variant	MED16	GRCh38.p7	19:883457	AGAGCTGGGCATGGC[A/G]GGGACCAAAGCCTGG	10025
rs374092709	snp	A/C			intron-variant	MED16	GRCh38.p7	19:870509	GACGTTGCAGTGGGC[A/C]AAGACGGCACTACTG	10025
rs374208942	snp	C/G			intron-variant	MED16	GRCh38.p7	19:872441	CTACAGCTGCGGGCC[C/G]GGGCCCCTGGTGACT	10025
rs374212106	snp	C/T			intron-variant	MED16	GRCh38.p7	19:878513	CCAGCCCCAGCCCCA[C/T]GTGCCCCAGCAGCTC	10025
rs374265478	snp	A/C/G	5.08284e-05	0.00504103	synonymous-codon	MED16	GRCh38.p7	19:872074	AAGCATGCCCAGCGA[A/C/G]GTGCCGTCCCGCAGA	10025
rs374273314	snp	A/G	0.000153988	0.00877327	intron-variant	MED16	GRCh38.p7	19:885023	CCTGCGGGGGAGGTG[A/G]GGGTGAGGGCTGACC	10025
rs374316201	snp	C/T			intron-variant	MED16	GRCh38.p7	19:870968	GGAGCCGTGTGGATT[C/T]GGGGGTCCCGGGGCA	10025
rs374360521	snp	A/G	0.000153988	0.00877328	synonymous-codon, utr-variant-5-prime	MED16	GRCh38.p7	19:891084	CCACTCACAGACGTA[A/G]GCCAAGTCCATCATC	10025
rs374371374	snp	C/T	1.69192e-05	0.00290849	synonymous-codon, intron-variant	MED16	GRCh38.p7	19:889650	CACCTTCTCCACGTG[C/T]AGGGCCAGTTTCACA	10025
rs374382865	snp	C/T			intron-variant	MED16	GRCh38.p7	19:878749	CCAGGGCCAGCCCCA[C/T]GTGCCCCAGCAGCTC	10025
rs374404076	snp	C/G	1.92981e-05	0.00310623	missense	MED16	GRCh38.p7	19:880044	GCTTCATGGCCGGCT[C/G]ATCCACAGGCCTCGG	10025
rs374404779	snp	A/T	1.97705e-05	0.00314402	missense	MED16	GRCh38.p7	19:886123	CGATCCAGCCCTCCA[A/T]GGGCTTGCCGCCGAA	10025
rs374408013	snp	C/G	0.000135566	0.00823192	missense	MED16	GRCh38.p7	19:871074	GGGTGGCAGCACTGC[C/G]AGGCAGCGTGGGCGC	10025
rs374441996	snp	C/T			intron-variant	MED16	GRCh38.p7	19:884461	CAGCCTCAGCTGACC[C/T]GCTGAGCCTTGGCTT	10025
rs374449776	snp	A/G			intron-variant	MED16	GRCh38.p7	19:878192	CGAGCCCAGCCCCAC[A/G]TGCCCCAGCAGCTCA	10025
rs374459668	snp	A/G	6.67947e-05	0.00577866	synonymous-codon	MED16	GRCh38.p7	19:881662	CACACGGTCCAGATC[A/G]TTGGTGGCCGATAGG	10025
rs374465962	snp	A/G			intron-variant	MED16	GRCh38.p7	19:875035	CGGGCGTGGTGGCAC[A/G]TGCCTGTAATCCCAG	10025
rs374474793	snp	A/G	1.70586e-05	0.00292045	intron-variant	MED16	GRCh38.p7	19:868520	GGGAGGCAGGCACTG[A/G]GCGGGTTCCCACTTC	10025
rs374480162	snp	A/G			intron-variant	MED16	GRCh38.p7	19:882048	CCCTAACACTCGCTC[A/G]GCCTTAGCCAGCTCA	10025
rs374480314	snp	A/G	0.000274411	0.0117103	intron-variant	MED16	GRCh38.p7	19:875500	GGCCGGAGCAGAGGC[A/G]CCCGCCAAGGCTCCA	10025
rs374486555	snp	A/G	1.66732e-05	0.00288727	synonymous-codon	MED16	GRCh38.p7	19:875314	AGGCGTGTTGAGAAA[A/G]TGGGGGCGCAGCAGC	10025
rs374540155	snp	A/G	0.000937332	0.0216284	intron-variant	MED16	GRCh38.p7	19:868301	GAGTCCAGGGCGAGC[A/G]GTGGCTCTTGCAGCA	10025
rs374542309	snp	A/G	7.25365e-05	0.00602187	synonymous-codon, intron-variant	MED16	GRCh38.p7	19:877175	TGAGAGGCGGAGCAC[A/G]CTCAGCTGCCAGAGA	10025
rs374542728	snp	C/T	0.000299805	0.0122398	intron-variant	MED16	GRCh38.p7	19:885737	GCTTCATTCCAAGCC[C/T]GCCAGCCCACGTGAT	10025
rs374561871	snp	G/T			upstream-variant-2KB	MED16	GRCh38.p7	19:894584	CAGTTCTCCAAGAGG[G/T]CCACGCAGTGACCTT	10025
rs374588467	in-del	-/GCGGG			intron-variant	MED16	GRCh38.p7	19:871860	AGGGGAGAGCGGGGA[-/GCGGG]GAGCGGGGAGAGGGG	10025
rs374612868	snp	C/T	0.00270495	0.0366764	intron-variant	MED16	GRCh38.p7	19:873426	AGGTGGGGGGCGGGG[C/T]CTTAGGGGAGAGCAT	10025
rs374639260	snp	A/G	0.000376034	0.0137068	intron-variant	MED16	GRCh38.p7	19:885049	TGACCCGGCACTGCT[A/G]TGGTGGCCACGCCAC	10025
rs374644066	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:871585	CACACAACCCGACAA[A/G]GAGAGACAGCAAACA	10025
rs374697348	snp	A/C	0.00318978	0.0398085	intron-variant	MED16	GRCh38.p7	19:885061	GCTGTGGTGGCCACG[A/C]CACCACCGGAGCCTG	10025
rs374763167	snp	A/G	0.000116857	0.00764295	synonymous-codon	MED16	GRCh38.p7	19:881641	CTTGGGCAGCGCCAC[A/G]GCCGACACACGGTCC	10025
rs374843121	snp	C/T			intron-variant	MED16	GRCh38.p7	19:869337	GGGACTTCCACACCA[C/T]CTCTGCCCAGACACC	10025
rs374847522	snp	A/G/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:877335	GTGTCTGTAGCGTCT[A/G/T]TACCTTTCTGTCAGG	10025
rs374864654	snp	A/C/G/T	0.00012638	0.00794845	intron-variant	MED16	GRCh38.p7	19:890927	GGGCGGGACACCATG[A/C/G/T]GGCCGGGAGGGGAAG	10025
rs374885842	snp	C/T	3.41413e-05	0.00413153	intron-variant	MED16	GRCh38.p7	19:890958	CAGGTGGGAGGGGGA[C/T]GCACCCTGGTCATCG	10025
rs374949217	snp	A/G	0.000135318	0.0082244	synonymous-codon	MED16	GRCh38.p7	19:881710	TGTGGGCTGTTTGTC[A/G]CCAACTGAAAAATCA	10025
rs374967072	snp	A/G			downstream-variant-500B	MED16	GRCh38.p7	19:867890	TTAAAGACAGGCCAA[A/G]AGGACACAGGCTCCC	10025
rs374975711	snp	C/T			intron-variant	MED16	GRCh38.p7	19:875601	ACCTCAGCAACCTCA[C/T]GGCAAAACAGGTGCG	10025
rs374977264	snp	A/G	4.06281e-05	0.00450693	missense, intron-variant	MED16	GRCh38.p7	19:877152	TCCAGCGGGTGGCCC[A/G]TGGAAGGTGAGAGGC	10025
rs374984867	snp	A/G			intron-variant	MED16	GRCh38.p7	19:879455	GTGCCCCAGCAGCTC[A/G]CCTTCCCCTGGTTGT	10025
rs375040530	snp	C/T	2.25218e-05	0.00335565	missense	MED16	GRCh38.p7	19:884953	GGGAGTCCCTCCTTG[C/T]GCAGGGACCAGCACT	10025
rs375083232	snp	A/G			intron-variant	MED16	GRCh38.p7	19:882639	GCATGTGCGGCCAGT[A/G]GACAGGCCACGCCAC	10025
rs375129237	snp	G/T	0.000314232	0.0125306	missense	MED16	GRCh38.p7	19:880131	GGACGCTGCCGTCGT[G/T]GAAGGCCAGGGCCAG	10025
rs375140438	snp	A/G	0.000111798	0.00747574	intron-variant	MED16	GRCh38.p7	19:871647	ACCCACACAGAGCAT[A/G]GACCTGTGCTAGGAA	10025
rs375145071	snp	C/T	0.000153988	0.00877328	synonymous-codon	MED16	GRCh38.p7	19:881635	GGGCAGCTTGGGCAG[C/T]GCCACGGCCGACACA	10025
rs375151740	snp	C/T	1.67987e-05	0.00289811	missense	MED16	GRCh38.p7	19:885779	GTTCACCTGCTCCGA[C/T]ATGTCCCGGGCCAGG	10025
rs375159769	snp	C/T	3.51976e-05	0.00419495	missense	MED16	GRCh38.p7	19:871968	GGAAGAGCAGGGACA[C/T]GCTGTCCTGGGTATC	10025
rs375200158	snp	A/G	0.00398564	0.0444627	intron-variant	MED16	GRCh38.p7	19:883583	CCTGAGAAAGGCTGT[A/G]GCATGTGTGTGAGAC	10025
rs375203039	snp	A/C			intron-variant	MED16	GRCh38.p7	19:877911	CCAGCCCCAGCCCCA[A/C]GTGCCCCAGCAGCTC	10025
rs375217271	snp	A/C	0.0528381	0.153711	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:892881	AAACCCTGAGCCCCG[A/C]GCCCCGCGCCCCGCG	10025
rs375235758	snp	A/G/T	0.0010118	0.0224697	intron-variant	MED16	GRCh38.p7	19:871689	GCAGATATCAAGGCA[A/G/T]AGCCACTGCCACCTG	10025
rs375265310	snp	A/G			upstream-variant-2KB	MED16	GRCh38.p7	19:894113	CGATCTCAGCTCACT[A/G]CAACCTCCGCCTTCC	10025
rs375290182	snp	A/C/G	0.000159987	0.00894248	missense	MED16	GRCh38.p7	19:871211	AGGCAGCATTCATCC[A/C/G]CCAGCGCCTCGTCCG	10025
rs375314920	snp	A/G	0.00318978	0.0398085	intron-variant	MED16	GRCh38.p7	19:889564	GCTGGTGATGGAGAG[A/G]AGAGGGGCTGGCGGG	10025
rs375318842	snp	A/C/G	3.41403e-05	0.00413149	missense, synonymous-codon	MED16	GRCh38.p7	19:875409	CCGTGCAGGGCGACA[A/C/G]CTTGCAGAGCGAGGC	10025
rs375334026	snp	A/G			intron-variant	MED16	GRCh38.p7	19:878316	CAGCCCCAGCCCCAC[A/G]TGCCCCAGCAGCTCA	10025
rs375347891	snp	C/T			intron-variant	MED16	GRCh38.p7	19:888072	AGCCGGGCGTGGTGG[C/T]GGGCGCCTGTAATCC	10025
rs375383535	snp	A/G			intron-variant	MED16	GRCh38.p7	19:888954	CACGAACATCCCCGA[A/G]ACCCTGCCGTCAGTG	10025
rs375436968	snp	A/G	0.00318978	0.0398085	intron-variant	MED16	GRCh38.p7	19:869959	GGTTTCCTCACCGTG[A/G]AATGGGGTGACAAGG	10025
rs375446206	snp	C/G			intron-variant	MED16	GRCh38.p7	19:877847	AATGCCCACCAAGCC[C/G]AGCCCCACATGCCCC	10025
rs375447353	snp	A/G	0.00160299	0.0282653	synonymous-codon	MED16	GRCh38.p7	19:871171	CAGCCAGTCCAGGCT[A/G]GGGATAAGCAGCTGG	10025
rs375452369	snp	A/C	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:881079	CTCTTTCCAGGGAAC[A/C]AGGGAAGAACGGGAG	10025
rs375461770	snp	A/G			intron-variant	MED16	GRCh38.p7	19:869242	GACGAGGGTCGGTCC[A/G]CCACGTGCCCGGGGA	10025
rs375504673	snp	C/T			intron-variant	MED16	GRCh38.p7	19:883774	TGCAGCCACACGGGG[C/T]GGCGCCAGGTGCTGC	10025
rs375510048	in-del	-/CACACGCCTG			intron-variant	MED16	GRCh38.p7	19:882395	GGTGATGCACGCCTG[-/CACACGCCTG]TAGTCCCAGCTACTC	10025
rs375553045	snp	A/C	2.13158e-05	0.00326458	missense	MED16	GRCh38.p7	19:879966	CAATCCCCACCAGGG[A/C]CAGTGACGTCCACGA	10025
rs375571894	snp	A/G	1.66236e-05	0.00288297	synonymous-codon	MED16	GRCh38.p7	19:885824	GATGGCGGGAAACTT[A/G]TCCTTGCGGTTGAGG	10025
rs375632523	in-del	-/CCAGCC			intron-variant	MED16	GRCh38.p7	19:878232	GGTTGTCAATGCCCA[-/CCAGCC]CCAGCCCCAGCCCCA	10025
rs375647224	snp	A/G	1.78353e-05	0.00298619	intron-variant	MED16	GRCh38.p7	19:881524	CCCCTGGTGTGAACT[A/G]AGGCCCCGCGTGGCT	10025
rs375657697	snp	A/G	1.66693e-05	0.00288693	missense	MED16	GRCh38.p7	19:875330	TGGGGGCGCAGCAGC[A/G]ACTTCAGGGTGGAGC	10025
rs375672058	snp	A/G	0.00398564	0.0444627	intron-variant	MED16	GRCh38.p7	19:880794	GGCGTGGCAGCACGC[A/G]CCTGTAGTCCCAGCT	10025
rs375679577	snp	C/G	0.00438332	0.0466095	intron-variant	MED16	GRCh38.p7	19:873773	GCCCACTGCCTGCCC[C/G]CCCCCGGGGGCCGCT	10025
rs375719188	snp	A/G			intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:892295	TTCAGCCCCACCCCT[A/G]ACCCCCTTTGCTTCC	10025
rs375746611	snp	C/T	5.79912e-05	0.00538444	intron-variant	MED16	GRCh38.p7	19:879923	CCCCGGCCCCACGTG[C/T]CCCAGCAGCTCACCT	10025
rs375749711	snp	A/C/G	0.000185964	0.00964126	intron-variant	MED16	GRCh38.p7	19:877189	CGCTCAGCTGCCAGA[A/C/G]ACAGAGCCCAAGGAG	10025
rs375750252	snp	C/G	0.0004567	0.0151044	utr-variant-3-prime	MED16	GRCh38.p7	19:868089	CACAAGGTCCGCCTG[C/G]ACCCCCGGCCGTCAC	10025
rs375751633	snp	A/C/G	3.88208e-05	0.00440559	intron-variant	MED16	GRCh38.p7	19:871580	ACATACACACAACCC[A/C/G]ACAAGGAGAGACAGC	10025
rs375771426	snp	A/C/G	0.00119737	0.0244387	upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:893478	TGGTGGTGGAACTCA[A/C/G]TATTCGTGCTCGCTT	10025
rs375798476	snp	C/T			intron-variant	MED16	GRCh38.p7	19:884368	GTGCGGGGGGCCCAT[C/T]GGGCGGATAGAGATG	10025
rs375804920	snp	A/C/G	0.00892749	0.066222	intron-variant	MED16	GRCh38.p7	19:868850	GGAGTCAGCGGTTCC[A/C/G]GGGGCCCCTCACCTG	10025
rs375809891	snp	C/T			intron-variant	MED16	GRCh38.p7	19:876535	CTTACCTGTGGGGCT[C/T]AACGTGTTACAGAAG	10025
rs375872831	snp	A/C/G	0.000434487	0.014733	intron-variant	MED16	GRCh38.p7	19:871674	GGAACTGGGGAAATA[A/C/G]CAGATATCAAGGCAG	10025
rs375916656	snp	A/G	0.00279162	0.0372561	intron-variant	MED16	GRCh38.p7	19:874621	TGTCGGCCTGGGAGC[A/G]TCTCAGCCCCCAGGA	10025
rs375959079	snp	A/G			intron-variant	MED16	GRCh38.p7	19:878384	CAGCCCCAGCCCCAC[A/G]TGCCCCAGCAGCTCA	10025
rs376018537	snp	C/G			intron-variant	MED16	GRCh38.p7	19:872850	GGCTGAGAAGGAGCA[C/G]GGCCTGGGAGGCGGG	10025
rs376056636	snp	A/G	0.00358779	0.0422022	intron-variant	MED16	GRCh38.p7	19:881158	AGCTGAGCAAATAGG[A/G]TAGGCACTGAAGAGT	10025
rs376107227	snp	A/G			intron-variant	MED16	GRCh38.p7	19:887559	TAATTCCAGCTACTC[A/G]GGAGGCTGAGGCAGG	10025
rs376132211	snp	A/C			intron-variant	MED16	GRCh38.p7	19:869117	CGGGACCACCTGAGA[A/C]AGGCCCAGTAAAGGG	10025
rs376148180	snp	A/G			intron-variant	MED16	GRCh38.p7	19:875689	TGGTGGGGGCCCCTG[A/G]TGATGTCTGGAGATA	10025
rs376157919	snp	A/C	7.76468e-05	0.00623036	missense	MED16	GRCh38.p7	19:871929	GGGGTGCCTCACAGC[A/C]GATCCAGAGCTTGGT	10025
rs376286071	snp	C/T	3.41956e-05	0.00413481	intron-variant	MED16	GRCh38.p7	19:868296	GAGGAGAGTCCAGGG[C/T]GAGCGGTGGCTCTTG	10025
rs376316811	snp	A/C/G	0.00376476	0.0432239	intron-variant	MED16	GRCh38.p7	19:885013	CACAAAAGCACCTGC[A/C/G]GGGGAGGTGGGGGTG	10025
rs376336371	snp	A/G			intron-variant	MED16	GRCh38.p7	19:872653	ACAGAGTGTACCGGC[A/G]GGGGGGTGGGGGCGA	10025
rs376356850	snp	C/T	8.4553e-05	0.00650149	missense	MED16	GRCh38.p7	19:868495	GCATGGTGACACAGC[C/T]GCACCTGCGGGGAGG	10025
rs376368245	snp	A/G	0.000251045	0.0112009	missense	MED16	GRCh38.p7	19:875442	TCATGGCCAGGATCC[A/G]GGTGGAGAGGACCTG	10025
rs376460813	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:884797	CGATCGCTTAGGGCC[A/G]GGGTTCAGGACCACC	10025
rs376507965	snp	A/G	0.000401284	0.0141591	intron-variant	MED16	GRCh38.p7	19:870990	CCCGGGGCAGGACAC[A/G]GAGGAAGGAGTCCTG	10025
rs376531755	in-del	-/CGCGGTGG			intron-variant	MED16	GRCh38.p7	19:887526	CAAAAATTAGCCGGG[-/CGCGGTGG]TGCGTGCCTGTAATT	10025
rs376533585	snp	A/G			intron-variant	MED16	GRCh38.p7	19:890956	AGCAGGTGGGAGGGG[A/G]ACGCACCCTGGTCAT	10025
rs376540676	snp	C/G	0.000153988	0.00877328	missense	MED16	GRCh38.p7	19:868445	CCAGCGCTGCTCCCA[C/G]TGCTTCACCGCCGTG	10025
rs376557186	snp	C/T	3.9412e-05	0.00443897	missense	MED16	GRCh38.p7	19:886020	AGGGCCACGCGGCCG[C/T]GCAGCCGGCACAGGC	10025
rs376558419	snp	C/G	0.290718	0.246662	intron-variant	MED16	GRCh38.p7	19:879821	TCAATCCCCACCAGG[C/G]CCAGCCCCACGTGCC	10025
rs376567444	snp	A/C/G	3.40142e-05	0.00412383	missense, synonymous-codon, intron-variant	MED16	GRCh38.p7	19:877027	GCAGCTTCTCCACCA[A/C/G]GCTCTGTACCATACT	10025
rs376569068	snp	C/T	2.26145e-05	0.00336255	missense	MED16	GRCh38.p7	19:868180	GACTGCGGGCCCAGC[C/T]GGACAAAGGCAGGGG	10025
rs376598392	snp	G/T			intron-variant	MED16	GRCh38.p7	19:877645	TCTGGCACCCTCCCA[G/T]CCCCAGCCCCAGCCC	10025
rs376626904	snp	A/G	4.52172e-05	0.00475463	synonymous-codon	MED16	GRCh38.p7	19:884957	GTCCCTCCTTGCGCA[A/G]GGACCAGCACTCCAC	10025
rs376638410	snp	A/G	0.00279162	0.0372561	intron-variant	MED16	GRCh38.p7	19:874934	TTAGGAGGCCGAGGC[A/G]GGCGGATCATTTGAG	10025
rs376654451	snp	C/T	0.000133147	0.00815817	missense	MED16	GRCh38.p7	19:871230	GCGCCTCGTCCGGCT[C/T]GCTCGCTGGGCCCTC	10025
rs376663922	snp	A/G	9.92113e-05	0.00704243	missense, utr-variant-5-prime	MED16	GRCh38.p7	19:890214	TCCCAGGGGTGCTCC[A/G]TGTCCAGGATGTGGA	10025
rs376670615	snp	C/T	0.00026062	0.0114124	synonymous-codon	MED16	GRCh38.p7	19:871225	CACCAGCGCCTCGTC[C/T]GGCTCGCTCGCTGGG	10025
rs376672604	snp	A/C			intron-variant	MED16	GRCh38.p7	19:879615	TGGTTGTCAATGCCC[A/C]CCAAGCCCAGCCCCA	10025
rs376733954	snp	A/G	0.00143827	0.0267781	missense	MED16	GRCh38.p7	19:871251	CTGGGCCCTCATCGC[A/G]ACCTGCGGAGAGAGG	10025
rs376767001	snp	A/G	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:873727	GAACGAGAAGGGGGC[A/G]ATGGCGTTGCCGGAC	10025
rs376802874	snp	C/G/T	0.000409883	0.0143109	synonymous-codon	MED16	GRCh38.p7	19:871087	GCCAGGCAGCGTGGG[C/G/T]GCCCGGCCAAACTGC	10025
rs376810168	in-del	-/CCAGCCCCAGCC			intron-variant	MED16	GRCh38.p7	19:878356	GGTTGTCAATGCCCA[-/CCAGCCCCAGCC]CCAGCCCCAGCCCCA	10025
rs376850879	snp	A/G			intron-variant	MED16	GRCh38.p7	19:881246	CTGCTGCAGCACAGA[A/G]AGGACACATGCCGCC	10025
rs376856600	snp	C/T			intron-variant	MED16	GRCh38.p7	19:878541	CTCACCTTCCCGTGG[C/T]TGTCAATGCCCACCA	10025
rs376858509	snp	C/T	8.18297e-05	0.00639595	synonymous-codon	MED16	GRCh38.p7	19:879979	GGCCAGTGACGTCCA[C/T]GATAGCTGCATAGCC	10025
rs376924513	snp	A/G			intron-variant	MED16	GRCh38.p7	19:877263	GGGCCCTGGGGCTGC[A/G]GCACGTGTGTGGATC	10025
rs376971044	in-del	-/C			intron-variant	MED16	GRCh38.p7	19:889152	CCTACTCTTAACTGT[-/C]CCCCCCAACCCTGGC	10025
rs376982904	in-del	-/GAG	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:875519	GCCAAGGCTCCAGCT[-/GAG]GAGAAGAGCAGTTCG	10025
rs376991389	snp	A/G			intron-variant	MED16	GRCh38.p7	19:879207	GCAGCTCACCTTCCC[A/G]TGGTTGTCAATGCCC	10025
rs377085988	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	MED16, RNU6-9	GRCh38.p7	19:893532	GAACGATACAGAGAA[A/G]ATTAGCATGGCCCCT	10025
rs377098431	snp	C/G	0.000153988	0.00877328	missense	MED16	GRCh38.p7	19:875288	GTCAGCCGGTCGCCG[C/G]GGCTCTTGTCAGGCG	10025
rs377113997	snp	A/G/T	0.000137618	0.00829397	missense	MED16	GRCh38.p7	19:871131	GCTTGGGCTGCAGGC[A/G/T]GCTAACCAGGCCGTC	10025
rs377198439	snp	A/G	0.00398564	0.0444627	intron-variant	MED16	GRCh38.p7	19:876838	GGGCCCCTGCCTGCC[A/G]CAGGGACAGCCCCAC	10025
rs377202129	in-del	C/TTT			upstream-variant-2KB, downstream-variant-500B	MED16, RNU6-9	GRCh38.p7	19:893592	CGTTCCATATTTTTT[C/TTT]TTTTTTCCATTTTCC	10025
rs377414684	snp	A/G	0.000219106	0.0104645	intron-variant	MED16	GRCh38.p7	19:890104	TCCGGGATCCGGGTC[A/G]CCACCCCTGGCCACG	10025
rs377415883	snp	A/G			downstream-variant-500B	MED16	GRCh38.p7	19:867665	ACAGAGAAGTGCAGA[A/G]ATACCAGAGACACGC	10025
rs377473004	snp	A/G	0.00398564	0.0444627	intron-variant	MED16	GRCh38.p7	19:884235	AGGCCCGCAGCCTCC[A/G]AGGCTCTGAAAACCA	10025
rs377477267	snp	A/G	0.0634824	0.166467	intron-variant	MED16	GRCh38.p7	19:879912	ATGCCCACCAGCCCC[A/G]GCCCCACGTGCCCCA	10025
rs377516600	snp	A/C	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:874136	ATTTTTTTTTTGAGA[A/C]AGAGTCTCACTCTGT	10025
rs377607914	snp	C/T			intron-variant	MED16	GRCh38.p7	19:876678	TTGCCCTCCGCCTGC[C/T]ATAGAGCCCCCAACC	10025
rs377639572	snp	A/G	4.17859e-05	0.00457069	intron-variant	MED16	GRCh38.p7	19:885026	GCGGGGGAGGTGGGG[A/G]TGAGGGCTGACCCGG	10025
rs377662708	snp	A/C/G/T	0.000150367	0.00866979	intron-variant	MED16	GRCh38.p7	19:873602	AAGGAGACGTGGGTC[A/C/G/T]GGTCAGCTCGGGCCT	10025
rs377668622	snp	A/G	3.95405e-05	0.0044462	missense, utr-variant-5-prime	MED16	GRCh38.p7	19:886125	ATCCAGCCCTCCATG[A/G]GCTTGCCGCCGAACA	10025
rs377680600	snp	A/G/T	0.000358596	0.0133861	intron-variant	MED16	GRCh38.p7	19:871917	GAGGGGCGGGCGGGG[A/G/T]TGCCTCACAGCAGAT	10025
rs377684359	snp	A/G	0.00398564	0.0444627	intron-variant	MED16	GRCh38.p7	19:870677	GAGTTAGGGGCACCT[A/G]GAAGGAAGCAGCAGT	10025
rs377685775	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:877939	CTCACCTTCCCGTGG[C/T]TGTCAATGCCCACCA	10025
rs377710036	snp	A/C/G	0.00159617	0.0282053	intron-variant	MED16	GRCh38.p7	19:872450	CGGGCCCGGGCCCCT[A/C/G]GTGACTGTACTGGGA	10025
rs377711766	snp	A/G			intron-variant	MED16	GRCh38.p7	19:878514	CAGCCCCAGCCCCAC[A/G]TGCCCCAGCAGCTCA	10025
rs377712696	snp	A/G	0.00199481	0.0315187	intron-variant	MED16	GRCh38.p7	19:869115	TGCGGGACCACCTGA[A/G]ACAGGCCCAGTAAAG	10025
rs377739246	snp	A/G/T	0.000197687	0.00994004	intron-variant	MED16	GRCh38.p7	19:870994	GGGCAGGACACGGAG[A/G/T]AAGGAGTCCTGTGTT	10025
rs377740939	snp	C/T	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:883279	AAGAGCTGGGCATGG[C/T]GGGGACCGAAGCCTG	10025
rs377743333	snp	C/G	0.00199481	0.0315187	intron-variant	MED16	GRCh38.p7	19:881380	CCCGAAAGATGAGAT[C/G]TGCCTCCTAATTGGG	10025
rs386805695	multinucleotide-polymorphism	AAG/GCC			intron-variant	MED16	GRCh38.p7	19:890495	ATGTGAACAGTGGGA[AAG/GCC]TCTCCACAGCAGATA	10025
rs397833265	snp	A/C	0.0704125	0.17392	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:892902	gagccccgcgccccg[A/C]gccccgcgccccgcg	10025
rs397970470	in-del	-/G			intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:891698	GTGGCCGAGGCGGGG[-/G]CTGAGTGTGACGGGG	10025
rs527316222	snp	C/G	0.000812414	0.0201382	synonymous-codon	MED16	GRCh38.p7	19:879955	CCCGTGGCTGTCAAT[C/G]CCCACCAGGGCCAGT	10025
rs527399567	snp	A/G	0.00279162	0.0372561	intron-variant	MED16	GRCh38.p7	19:882886	CAAACCCGTATAGGG[A/G]TCCTGTGAGCAGCAT	10025
rs527399684	snp	C/G	0.00199481	0.0315187	intron-variant	MED16	GRCh38.p7	19:879561	GCCCCAGCAGCTCGC[C/G]TTCCCCTGGTTGTCA	10025
rs527568930	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:893451	ACATTTGTTCCAGGG[A/G]CTTTAAATAGCTGGT	10025
rs527571737	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:885238	CCACAGGGACAGCAA[A/G]GGGACACAGGGAACC	10025
rs527593890	in-del	-/A	0.00159617	0.0282053	intron-variant	MED16	GRCh38.p7	19:886922	GCTAATAAAAAATAC[-/A]AAAAAAATTAGCCGG	10025
rs527594927	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:869848	CTGAAACAGGCTGGG[A/G]GTCTGACGGGCCTGG	10025
rs527604347	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	MED16	GRCh38.p7	19:867574	CAACCTCCAGCAGAG[A/G]GCAGCTGGAGAAACA	10025
rs527618338	snp	C/T			intron-variant	MED16	GRCh38.p7	19:876893	GGCCCCCACCTGCCA[C/T]GGGGCCCCACCTGCC	10025
rs527630117	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	MED16	GRCh38.p7	19:894654	ACGTTCTTAGCGGCC[C/T]GGGTGTGGTGGCACA	10025
rs527635909	snp	C/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:880203	AGGACACGCCCGCCG[C/G]GGGAGGGGCCTCCTG	10025
rs527640688	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:883612	ACGTGGCTCTCGGGC[A/G]GGTAACAGCTGGGCC	10025
rs527728068	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:886365	TGGGATGTGATCCCC[C/T]CTGACCCTCCGTCTC	10025
rs527729710	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:883339	AGAGCTGGGCATGGC[A/G]GGGACCGAAGCCTGG	10025
rs527762436	snp	C/T	3.42824e-05	0.00414005	intron-variant	MED16	GRCh38.p7	19:889858	GGATGGGCAGAGCAC[C/T]GCGTTGCAGGACGGC	10025
rs527765477	snp	C/T	0.000121372	0.00778916	synonymous-codon	MED16	GRCh38.p7	19:886046	CAGGCTCTCGGTGGA[C/T]GTCAGCACCTGCCCG	10025
rs527854029	snp	A/G	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:889470	CCTCAGTTAAATGAG[A/G]GGCCACTGAACACAC	10025
rs527882621	snp	A/G	0.00597247	0.0543191	utr-variant-5-prime, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:893141	GCGATCTTCCCTAGC[A/G]CCTCGGGTCTGGCGC	10025
rs527882641	snp	A/C	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:889157	TCTTAACTGTCCCCC[A/C]CAACCCTGGCCACGC	10025
rs527917843	snp	A/G	0.00795532	0.062565	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:891553	AAGAGCCCGCAGACA[A/G]GCAAGCGGTGGGGCG	10025
rs527968710	snp	G/T	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:892715	CTCTACAGCCCCCCA[G/T]TCCCCAGGCTCCACC	10025
rs527999548	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:875577	CTGGGCAAGCTGCTT[C/T]GCCTCTGCACCTCAG	10025
rs528044716	snp	C/T	0.000399281	0.0141238	synonymous-codon	MED16	GRCh38.p7	19:881632	GATGGGCAGCTTGGG[C/T]AGCGCCACGGCCGAC	10025
rs528063794	snp	A/G	0.000231803	0.0107633	intron-variant	MED16	GRCh38.p7	19:884870	CGCCCCCGAGGGCAG[A/G]CCCAGGGCCTCCGCA	10025
rs528133848	snp	A/G	0.0023933	0.0345097	intron-variant	MED16	GRCh38.p7	19:884703	AGGATGGAGGAGTCT[A/G]TACGCCTAACACACT	10025
rs528218678	snp	C/T			intron-variant	MED16	GRCh38.p7	19:888876	GCCTCCTAGTTCCTG[C/T]GAGAGCCCCAGCACA	10025
rs528275588	snp	A/G	0	0	upstream-variant-2KB	MED16	GRCh38.p7	19:894701	ACTTTGGGAGGCCAA[A/G]GTCTGAGGACAGCTT	10025
rs528292717	snp	C/T	0.00159617	0.0282053	intron-variant	MED16	GRCh38.p7	19:871487	CATGAGACTCCCTCA[C/T]TCACTTAAAAAGTAT	10025
rs528331323	snp	A/G	0.000399281	0.0141238	synonymous-codon	MED16	GRCh38.p7	19:871198	CTGGCTGGGCAGCAG[A/G]CAGCATTCATCCACC	10025
rs528462911	snp	A/C	0.00318978	0.0398085	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:891531	GACACTAGCTCTCTC[A/C]CGAAGGAAGAGCCCG	10025
rs528497711	snp	A/C/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:891303	GCCTGGGGCTGGGGC[A/C/G]GAGGGGGAACATGGA	10025
rs528502736	snp	A/G	0.00279162	0.0372561	intron-variant	MED16	GRCh38.p7	19:871815	GGAGAGCGGGGAGAG[A/G]GGAGAGCGGGGAGAG	10025
rs528610663	snp	A/G	0.00716266	0.059414	intron-variant	MED16	GRCh38.p7	19:874565	CTTACGGCAAAACGG[A/G]AGGAGGAGCAGACCT	10025
rs528645703	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:877852	CCACCAAGCCCAGCC[C/T]CACATGCCCCAGCAG	10025
rs528727159	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:877469	TACCCCGTGAAAGGC[A/G]GTCCTCTCAACAGCT	10025
rs528833763	snp	C/T	0.00279162	0.0372561	intron-variant	MED16	GRCh38.p7	19:889548	CAAAAAACCAGGGGA[C/T]GCTGGTGATGGAGAG	10025
rs528854472	snp	C/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:870702	AGCAGTCATGGCCAT[C/G]ACTGGAGAACATGGA	10025
rs528923158	snp	A/C	0.00199481	0.0315187	intron-variant	MED16	GRCh38.p7	19:875802	CAGAGGCTGCTCCAG[A/C]CCCCGATGTCTGTGG	10025
rs528942362	snp	C/T			intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:891545	CCCGAAGGAAGAGCC[C/T]GCAGACAGGCAAGCG	10025
rs528980014	snp	A/G	8.36841e-05	0.006468	missense	MED16	GRCh38.p7	19:875280	AGATCTCGGTCAGCC[A/G]GTCGCCGGGGCTCTT	10025
rs528999042	snp	C/G	0.00199481	0.0315187	intron-variant	MED16	GRCh38.p7	19:876113	GTCTCACGCGTTTCT[C/G]GGCAGGCTGTGCCGT	10025
rs529041716	snp	A/C	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:880484	GGTTGGGGCTCCTGG[A/C]GTCCCAAAGAGAGGC	10025
rs529137163	snp	C/G	2.67476e-05	0.00365692	intron-variant	MED16	GRCh38.p7	19:880178	CACTGCTTAGACATG[C/G]GCAGGGCCCAGGACA	10025
rs529191972	snp	C/G			missense	MED16	GRCh38.p7	19:884965	TTGCGCAGGGACCAG[C/G]ACTCCACGATGCTGC	10025
rs529234452	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:876966	CCCCACCTGCCACGG[A/G]CCCCCACCTGCTGCA	10025
rs529318878	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:881293	CCACCAAGTTCCCCA[A/G]GCTCCCTTGTTGATT	10025
rs529374487	snp	A/G	0.00557542	0.0525036	intron-variant	MED16	GRCh38.p7	19:880850	GAATCGCTTGAACCC[A/G]GGAGGCGGAGGTTGC	10025
rs529446571	snp	A/C			upstream-variant-2KB, nc-transcript-variant	MED16, RNU6-9	GRCh38.p7	19:893501	GCTCGCTTCGGCAGC[A/C]CATATACTAAAATTG	10025
rs529551025	snp	C/T	0.00199481	0.0315187	intron-variant	MED16	GRCh38.p7	19:870912	ATGGAGGCGGGGAGC[C/T]GTGTGGATTCGGGGG	10025
rs529554583	snp	C/T	0.000106866	0.00730901	intron-variant	MED16	GRCh38.p7	19:890118	CGCCACCCCTGGCCA[C/T]GTGGGACCAGCGCCT	10025
rs529607497	snp	A/G	0.0004251	0.0145729	intron-variant	MED16	GRCh38.p7	19:868347	AGCTGAGGGGTAGCT[A/G]AGGAGTAGCTGAGGG	10025
rs529624368	snp	A/C	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:889917	GAGAGGTCTCGGCCC[A/C]GGTAGGGCACAGCAG	10025
rs529649218	snp	C/T	0.0023933	0.0345097	intron-variant	MED16	GRCh38.p7	19:879481	GTTGTCAATGCCCAC[C/T]AGCCCCAGCCCCACG	10025
rs529689447	in-del	-/G	0.0205511	0.0992634	intron-variant	MED16	GRCh38.p7	19:885453	ACGGGAGAGCACGTT[-/G]GGGGGGGGTCCGGGG	10025
rs529701381	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:878086	GTCAATGCCCCCCAG[C/T]CCCAGCCCCAGCGCC	10025
rs529728663	snp	C/G	0.00279162	0.0372561	intron-variant	MED16	GRCh38.p7	19:885459	AGAGCACGTTGGGGG[C/G]GGTCCGGGGGCCCCA	10025
rs529814353	snp	A/G	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:885156	CCCTCCTGGATTCCA[A/G]CCCAGGCCTGTCCCC	10025
rs529852534	snp	C/G	0.00358779	0.0422022	intron-variant	MED16	GRCh38.p7	19:869007	GCCAGGTTCCGGCAG[C/G]GGCATCTGTCCACAG	10025
rs529929012	snp	A/T	3.8768e-05	0.00440255	missense	MED16	GRCh38.p7	19:880035	TGCGGGGGCGCTTCA[A/T]GGCCGGCTCATCCAC	10025
rs529933848	snp	C/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:887877	GATCAGGGTGATGCA[C/G]GATGGGGACTGGGTT	10025
rs529963199	snp	C/T	0.00676609	0.0577691	intron-variant	MED16	GRCh38.p7	19:869168	GGAGGGTTGGTCTCC[C/T]AGGTGCCTGGGGAGC	10025
rs529977030	snp	A/G	0.000298181	0.0122066	synonymous-codon, utr-variant-5-prime	MED16	GRCh38.p7	19:891021	TCGGCAGGACCAGGC[A/G]CAGGCCAGGGGCACC	10025
rs529997030	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:891243	AAACAATGGAGGCCC[A/G]TGGTAGAGGGAACAG	10025
rs530007508	snp	A/G	0.0142736	0.0832652	intron-variant	MED16	GRCh38.p7	19:871735	TGGCGGGGGGCTCAG[A/G]CAGGACTTGTGTTTT	10025
rs530035162	snp	A/G	5.53062e-05	0.00525833	synonymous-codon	MED16	GRCh38.p7	19:868128	CTCTGGATGCAGATG[A/G]TCCAGGGATCTGGGG	10025
rs530205320	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:889043	CTGGCCACGCCTACT[C/T]TTAACTGTCCCCCCC	10025
rs530246716	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:892553	TCTTCAGGCCCCGCC[C/T]CTATAACCCCCAATC	10025
rs530250385	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:891748	GGGCTGACTGACAGG[A/G]AACACCTGTGGCCGA	10025
rs530275493	snp	A/G			upstream-variant-2KB	MED16	GRCh38.p7	19:894735	TTTGAGACCAGCCTG[A/G]GAAACATAGCCAGAC	10025
rs530313545	snp	A/G	0.00159617	0.0282053	intron-variant	MED16	GRCh38.p7	19:872384	GAGGCTCTGGCTGAG[A/G]CCAATATCCCCACCT	10025
rs530404052	snp	C/T	0.00159617	0.0282053	intron-variant	MED16	GRCh38.p7	19:886273	TGACCCCCAGAAACA[C/T]GCGCACAGAAGAACC	10025
rs530446614	snp	A/G/T	0.000134626	0.00820352	intron-variant	MED16	GRCh38.p7	19:871586	ACACAACCCGACAAG[A/G/T]AGAGACAGCAAACAG	10025
rs530480049	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:868796	GAGCGCTGGGTGGGG[A/G]CTAGAATCAGCTGAG	10025
rs530492254	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:887438	TTTGGGAGGCCGAGG[C/T]GGGCAGATCTCAAGG	10025
rs530500263	snp	C/T	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:884354	GCTTGGCTCCGTGGG[C/T]GCGGGGGGCCCATCG	10025
rs530533298	snp	A/G	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:887170	GTATCGTACGGCTCC[A/G]TTCTAAGTTACAAGT	10025
rs530725204	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:870984	GGGGGTCCCGGGGCA[A/G]GACACGGAGGAAGGA	10025
rs530755183	snp	C/T	0.0021885	0.033007	intron-variant	MED16	GRCh38.p7	19:876952	CACCTGCCACGGGGC[C/T]CCACCTGCCACGGGC	10025
rs530756533	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, downstream-variant-500B	MED16, RNU6-9	GRCh38.p7	19:893622	TCCCTCCCAGAAACG[C/G]AATCTTGCTCTGTTG	10025
rs530931456	snp	A/G	0.00517822	0.0506191	intron-variant	MED16	GRCh38.p7	19:874050	ACCATGACTGTGCAC[A/G]CGGCTCCCAGCTACC	10025
rs530968899	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:877316	TGGGCCTGTGTGCGC[A/G]CATGTGTCTGTAGCG	10025
rs531056155	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:877459	CTGAGGAGTCTACCC[C/T]GTGAAAGGCGGTCCT	10025
rs531092827	snp	A/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:881802	CATGGCCTGGTGTGC[A/T]ACCTGCCCAGGGCCC	10025
rs531216854	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:884690	CAGCGGGCGTGGAAG[A/G]ATGGAGGAGTCTATA	10025
rs531237567	snp	A/G	0.00279162	0.0372561	intron-variant	MED16	GRCh38.p7	19:875616	TGGCAAAACAGGTGC[A/G]GAAGACCAGGCGCAC	10025
rs531292263	snp	A/C/G	0.00463884	0.0479549	intron-variant	MED16	GRCh38.p7	19:890414	GTCCCCCCGCAGGAA[A/C/G]AGAGCAGGCCTGTGA	10025
rs531324218	snp	C/T	3.33951e-05	0.00408613	missense	MED16	GRCh38.p7	19:875375	AAGAGCTTGGTGTGG[C/T]AGTCGCACACGCGGG	10025
rs531330512	snp	A/C	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:872819	GCAAGGCGAACCGGC[A/C]TTCGTGTAGGGGTGG	10025
rs531358282	snp	A/G/T	0.000118616	0.00770034	synonymous-codon	MED16	GRCh38.p7	19:880006	AGCCTTTAAGTGGAC[A/G/T]GCGGGGCCCGCGGTG	10025
rs531576229	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:882938	AGAGAGTGGCTGAGA[C/T]GCCCAGAGGGCACAC	10025
rs531608044	snp	C/G			intron-variant	MED16	GRCh38.p7	19:883887	GACCGGGCGAAGGAA[C/G]GAGCCCTGGGAGAAG	10025
rs531656068	snp	A/C	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:883909	TGGGAGAAGGAATGG[A/C]AGCAGCCCTCTTCAC	10025
rs531678455	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:886685	CTGTGTAAGCACCAG[C/T]GGCTGCTGCGGGCAC	10025
rs531740837	snp	A/G	0.0023933	0.0345097	intron-variant	MED16	GRCh38.p7	19:869082	GGCCCAGATGTCTGT[A/G]AACAGTGAGGTGGGA	10025
rs531800134	snp	A/G	0.00279162	0.0372561	intron-variant	MED16	GRCh38.p7	19:889871	ACTGCGTTGCAGGAC[A/G]GCACAGCGCCTGGGG	10025
rs531877553	snp	A/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:870676	GGAGTTAGGGGCACC[A/T]AGAAGGAAGCAGCAG	10025
rs531880354	snp	C/T	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:889492	TGAACACACAGGTGC[C/T]AATGACAGCCGGACT	10025
rs531911399	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:893438	CCTATGTGTACAGAC[A/G]TTTGTTCCAGGGGCT	10025
rs531915617	snp	G/T	0.00517822	0.0506191	intron-variant	MED16	GRCh38.p7	19:873108	GGGAGGGCTCCGAGG[G/T]GGGGCAGGGCTCCGA	10025
rs532051711	snp	A/C/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:870494	TGAACCCGAGAGGCA[A/C/G]ACGTTGCAGTGGGCC	10025
rs532087368	snp	C/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:882226	TAGCAAATGTGACAT[C/G]GCCGGGCACAGCAGC	10025
rs532140277	snp	C/T	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:887812	TATGAATGTCCAGGA[C/T]AGGCAGATCCAGAGA	10025
rs532214346	snp	C/T			intron-variant	MED16	GRCh38.p7	19:882833	ATGAGGTCTCTGCCC[C/T]GGACGGGCCATCACG	10025
rs532263542	snp	A/C	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:890704	TCTCCAACAAGCCTC[A/C]GTCAACCAACGCTCC	10025
rs532308414	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:871542	GACACTGGGATGTAA[A/G]AATGACACAGCTCAC	10025
rs532344434	snp	C/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:869149	GCGGGACCCCCCACA[C/G]GGAGGAGGGTTGGTC	10025
rs532367003	snp	G/T	0.000399281	0.0141238	downstream-variant-500B	MED16	GRCh38.p7	19:867814	GTGTCCTGTCCCCAC[G/T]GCTCACTTTGGATAC	10025
rs532375877	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:885510	GGAGAGAATGTGGGA[A/G]GTTGAGATTCAGAGA	10025
rs532400388	snp	G/T	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:870170	TCTCCATCCACAGAG[G/T]GATCTACGGCGAGGC	10025
rs532407782	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:869025	CATCTGTCCACAGGC[A/G]GGGGTGGAGGGAATG	10025
rs532408805	snp	A/G			intron-variant	MED16	GRCh38.p7	19:870434	GGTGTGGTGGCTCAT[A/G]CCTGTAATCCCAGCT	10025
rs532551977	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:892319	TGCTTCCCACACTTC[A/C]TTTCACCCCTTGAGC	10025
rs532589211	snp	A/G	0.0364509	0.129988	intron-variant	MED16	GRCh38.p7	19:871846	GGGAGAGCGGGGAGA[A/G]GGGAGAGCGGGGAGC	10025
rs532598277	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:869862	GGGTCTGACGGGCCT[A/G]GGTTCAAATCCTGAC	10025
rs532745905	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:874839	TGCGTCACCGTGCTG[C/T]AACCTGGATGACACA	10025
rs532764026	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:868581	TTTGCTTCCAGGCAG[A/G]TCTCCCTCTGCTCGC	10025
rs532781526	snp	C/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:874598	CTGCACAGGACCCGG[C/G]TGCCGGGTGTCGGCC	10025
rs532783397	snp	A/G	0.00159617	0.0282053	intron-variant	MED16	GRCh38.p7	19:879275	CCTCTGGTTGTCAAT[A/G]CCCAGCAGCTCACCT	10025
rs532865215	snp	A/G	0.00159617	0.0282053	intron-variant	MED16	GRCh38.p7	19:870719	CTGGAGAACATGGAG[A/G]GAAGGAGCCGTATGG	10025
rs532903065	snp	A/C	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:886823	GCTCTCGCCTATAAT[A/C]CCAGCACTTTGGGGG	10025
rs532917687	snp	C/T	0.000399281	0.0141238	missense	MED16	GRCh38.p7	19:871142	AGGCGGCTAACCAGG[C/T]CGTCGCTGGCTGGCA	10025
rs532960163	snp	A/G	0.000399281	0.0141238	synonymous-codon, utr-variant-5-prime	MED16	GRCh38.p7	19:890159	GTCCCACTCCAGGCA[A/G]GTGATGGCCTCGTGG	10025
rs532960317	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, downstream-variant-500B	MED16, RNU6-9	GRCh38.p7	19:893926	ATGTCCAAGAGTGGG[A/G]AAACTGTAAGCGAAG	10025
rs532972960	snp	C/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:876587	AAACTGCTTCTCTGA[C/G]GTGCAGCTTTCCTGG	10025
rs533048311	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	MED16, RNU6-9	GRCh38.p7	19:893579	CAAATTCGTGAAGCG[A/T]TCCATATTTTTTTTT	10025
rs533140543	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:873228	AGACAGACTCAGGAA[A/G]TGGGACTCCAAGTAG	10025
rs533153746	snp	C/G			intron-variant	MED16	GRCh38.p7	19:886698	AGCGGCTGCTGCGGG[C/G]ACTATTTGATTTCAA	10025
rs533178244	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:876181	GGTTTCTGATGGCAC[A/G]GAGGAAAACAAGTGA	10025
rs533181722	snp	C/G	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:877308	CCCGTGTGTGGGCCT[C/G]TGTGCGCGCATGTGT	10025
rs533227856	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:872844	GGGTGGGGCTGAGAA[A/G]GAGCAGGGCCTGGGA	10025
rs533264171	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:881484	GAGCTCCCACGACCC[C/T]GTGGCCTGTGCTCAG	10025
rs533279117	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:880550	TGGGGTCTGCCATTG[C/T]ACGAGGGCCGGGGGG	10025
rs533305338	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:881325	GCAATGACTCTTTAC[A/G]TATTAAAGAACACTG	10025
rs533398133	snp	A/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:884247	TCCGAGGCTCTGAAA[A/T]CCAAGCGGCTGTTCT	10025
rs533482112	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:868752	CACTCCCTCTGGGAC[A/G]TGCTCCCTCCACCAC	10025
rs533543556	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:872179	TGGCGATGGGATGAA[A/G]TGTCTTGGGGTCGGT	10025
rs533558078	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:891445	CAGACCATGGGGGCC[A/G]AGGGCACAGCCGGGA	10025
rs533653475	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:883994	ACCTTTACTGCCTCT[A/G]CGGCCACAATGGGCA	10025
rs533701320	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:874440	AGAAACAGCCTGCCA[A/G]GCACAGTGGCTCACG	10025
rs533702934	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:874110	GTACTCCAGACAAAC[A/G]ATAACCCTAAATTTT	10025
rs533784915	snp	C/T	0.00716266	0.059414	intron-variant	MED16	GRCh38.p7	19:877586	GCAGGCAGGGGCTGG[C/T]GAGGGGCTTGCACCT	10025
rs533797832	snp	G/T	0.000800085	0.0199851	intron-variant	MED16	GRCh38.p7	19:871914	GGGGAGGGGCGGGCG[G/T]GGGTGCCTCACAGCA	10025
rs533811246	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:882024	ACCTCAGACCTGCAG[C/T]CATGCAAACCCTAAC	10025
rs534059894	snp	C/G			downstream-variant-500B	MED16	GRCh38.p7	19:867695	CAGAAACAAGGAGAG[C/G]ACGCAGAGACAGTAT	10025
rs534069563	in-del	-/CCGGCCCCGGCC			intron-variant	MED16	GRCh38.p7	19:878938	GCCCCGGCCCCGGCC[-/CCGGCCCCGGCC]GCAGCTCCACGTGCC	10025
rs534085326	snp	C/T	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:875733	CCACTGGGGGTGCCC[C/T]TGCCAAGTAACGGGT	10025
rs534140334	snp	A/G			intron-variant	MED16	GRCh38.p7	19:877634	GGGCGCCTCCCTCTG[A/G]CACCCTCCCAGCCCC	10025
rs534220692	snp	C/T			upstream-variant-2KB, downstream-variant-500B	MED16, RNU6-9	GRCh38.p7	19:893805	TTTCGCCATGTTGGC[C/T]AGGGTGGTCTCTATC	10025
rs534222657	in-del	-/A	0.307423	0.243316	intron-variant	MED16	GRCh38.p7	19:888525	CGAGACTCTGTCTCC[-/A]AAAAAAAAAAAAAAA	10025
rs534228455	snp	C/T	1.92702e-05	0.00310399	synonymous-codon	MED16	GRCh38.p7	19:880054	CGGCTCATCCACAGG[C/T]CTCGGGGCCGCGGAG	10025
rs534242015	snp	A/C/T	0.000179232	0.009465	missense	MED16	GRCh38.p7	19:868114	CGTCACGGACGGTCC[A/C/T]CTGGATGCAGATGGT	10025
rs534249958	snp	C/T	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:888493	CGCATCACTGCACTC[C/T]AGCCTGGGGGATAGA	10025
rs534265801	snp	A/G	0.0108824	0.0729573	intron-variant	MED16	GRCh38.p7	19:879889	AGCTCGCCTTCCCCT[A/G]GTTGTCAATGCCCAC	10025
rs534268200	snp	A/G	0.0023933	0.0345097	intron-variant	MED16	GRCh38.p7	19:882986	GGCCCTCATGGAATT[A/G]AGCCTCTCATAGGAA	10025
rs534293093	snp	C/T	0.00279162	0.0372561	intron-variant	MED16	GRCh38.p7	19:886558	TGGCTCTGGCTCTGC[C/T]GTGGCGGCACACAGG	10025
rs534358371	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:882826	CCGCATCATGAGGTC[C/T]CTGCCCCGGACGGGC	10025
rs534404218	snp	A/C	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:885552	TGCGCTGTGGCCACG[A/C]AGCGGGAGGAAGGCG	10025
rs534412257	snp	C/T			intron-variant	MED16	GRCh38.p7	19:871032	CAATGCAGGGACACA[C/T]GCACCTGGCGAGGCC	10025
rs534467639	snp	A/T	0.000399281	0.0141238	downstream-variant-500B	MED16	GRCh38.p7	19:867894	AGACAGGCCAAGAGG[A/T]CACAGGCTCCCGGCA	10025
rs534482972	snp	A/G	0.00318978	0.0398085	intron-variant	MED16	GRCh38.p7	19:880857	TTGAACCCAGGAGGC[A/G]GAGGTTGCAGTGAGC	10025
rs534495193	snp	A/G	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:888765	CGAAGCCGGTGCTGC[A/G]TGTACTGCGGCAATG	10025
rs534511538	in-del	-/AG	0.00517822	0.0506191	intron-variant	MED16	GRCh38.p7	19:874137	TTTTTTTTTTGAGAC[-/AG]AGTCTCACTCTGTCG	10025
rs534520486	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:869966	TCACCGTGAAATGGG[A/G]TGACAAGGTCCCACC	10025
rs534603609	snp	C/T	0.000399281	0.0141238	missense, utr-variant-5-prime	MED16	GRCh38.p7	19:890233	CCAGGATGTGGATCA[C/T]GCGGGTCAGGTCTGT	10025
rs534630384	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, downstream-variant-500B	MED16, RNU6-9	GRCh38.p7	19:893667	CAATGGCGCGATCTT[A/C]GCTTGTTGCAACCTC	10025
rs534685536	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:884419	GGCTGCTGGAGAGGT[A/G]GGGTGGGGTGGGGGG	10025
rs534797588	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:887641	ACTGCACTCCAGCCC[A/G]GTTGACAGAACAAGA	10025
rs534834461	snp	C/T	0.00199481	0.0315187	intron-variant	MED16	GRCh38.p7	19:890741	ATTCGATCCCGCACA[C/T]GGGGCGATCTCATGT	10025
rs534914077	snp	C/T	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:871317	CCCGGCCACCCGGGA[C/T]GTGCTGGGAGCCCCT	10025
rs535019649	snp	C/T	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:873811	GCACCAACCAGCTTC[C/T]CTCGGCCTGCAGGCC	10025
rs535109560	snp	G/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:889504	TGCTAATGACAGCCG[G/T]ACTGCAGGTGGGAGC	10025
rs535110834	snp	C/G	1.65723e-05	0.00287852	missense, utr-variant-5-prime	MED16	GRCh38.p7	19:891100	GCCAAGTCCATCATC[C/G]CACCTGCCGCTGGCC	10025
rs535119763	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:870514	TGCAGTGGGCCAAGA[C/T]GGCACTACTGCACTC	10025
rs535133300	snp	A/G			intron-variant	MED16	GRCh38.p7	19:890491	CGAAATGTGAACAGT[A/G]GGAGCCTCTCCACAG	10025
rs535178550	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:870289	AGGCAAGGCCGGGGC[A/G]GTGGCTCACACCTGT	10025
rs535193608	snp	A/C	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:893206	GCGTGGGGCCGCCTC[A/C]CAAAGACTTCTGGGA	10025
rs535246596	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:874112	ACTCCAGACAAACGA[C/T]AACCCTAAATTTTTT	10025
rs535246961	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	MED16	GRCh38.p7	19:894940	AATACAAAAATATTA[G/T]CTGGGCATGGTGACA	10025
rs535314415	snp	C/T	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:872301	GGACGCTGCTCAGAG[C/T]CCTGCAGGGCCCAGG	10025
rs535471999	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	MED16, RNU6-9	GRCh38.p7	19:893490	TCAATATTCGTGCTC[C/G]CTTCGGCAGCACATA	10025
rs535562922	snp	G/T	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:876278	CACTCTGGGATTGCA[G/T]GCACATAACCACACC	10025
rs535725851	snp	C/T	0.0103295	0.0711199	intron-variant	MED16	GRCh38.p7	19:883463	GGGCATGGCGGGGAC[C/T]AAAGCCTGGCATGGT	10025
rs535810983	snp	A/G	0.0138799	0.0821421	intron-variant	MED16	GRCh38.p7	19:870776	TGGAGGGAGGGAGCC[A/G]TGTGGATTCGGGGGG	10025
rs535810990	snp	C/G	0.000116714	0.00763829	synonymous-codon	MED16	GRCh38.p7	19:873557	AAATTCCTCCGTCTT[C/G]AGGTTGATCATGACC	10025
rs535900733	snp	C/T	0.0509478	0.151255	intron-variant	MED16	GRCh38.p7	19:873342	GGGCGGGACTCCAAC[C/T]AGGGGCGGGGCTGAG	10025
rs535929189	snp	C/T			intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:892151	GGCTGTTTCGCTTCG[C/T]AAAGGCAAAAGCCCA	10025
rs535988900	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:876092	AGCCTCGCAGCCCCC[A/G]CCTGGGTCTCACGCG	10025
rs535996580	snp	C/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:875942	CGTAGGACACCCCAT[C/G]TCTACAAAAAATAGA	10025
rs536136193	snp	G/T	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:884751	CGCGGTCACACCCGA[G/T]ATCCTAGCACTACTG	10025
rs536172832	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:887582	GAGGCAGGAGAATCA[C/T]TTGAACCTGGGAGGT	10025
rs536209157	snp	A/G	0.00165084	0.0286827	intron-variant	MED16	GRCh38.p7	19:881835	CCCAGGTCTCATGCC[A/G]CCCTGCTCCCATGCC	10025
rs536213907	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:871757	TTGTGTTTTGGTAGG[A/G]AGAGGGGAGCGGGGA	10025
rs536298495	in-del	-/A	0.00438332	0.0466095	intron-variant	MED16	GRCh38.p7	19:887665	ACAAGACTCTGTCTC[-/A]AAAAAAAATGTATTT	10025
rs536330992	snp	A/C	0.00398564	0.0444627	intron-variant	MED16	GRCh38.p7	19:877550	CTCAACAAGACGAAC[A/C]CATCACACAGACAAG	10025
rs536363404	snp	C/G	0.000798403	0.0199641	downstream-variant-500B	MED16	GRCh38.p7	19:867840	GATACCCCCAGACTC[C/G]GCATCCACTAGGTGC	10025
rs536366373	snp	A/G			intron-variant	MED16	GRCh38.p7	19:883218	TGAAGAGCTGGGCAT[A/G]GTAGGAACCGAAGCC	10025
rs536421189	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:881963	GGAAACCTGTGGGCC[A/G]GCACCATCTCACCCC	10025
rs536532249	snp	C/T			intron-variant	MED16	GRCh38.p7	19:869243	ACGAGGGTCGGTCCG[C/T]CACGTGCCCGGGGAG	10025
rs536548240	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:869308	ATTTGAGGCTGGACA[A/G]AAGCAGGTACATGGG	10025
rs536656292	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:882781	TGTTACTCGGCTGAA[A/G]CTGACTACCACGCAG	10025
rs536660271	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:884035	CCACCTGCAGGCCCC[A/G]GGAGCCATCGGGGCC	10025
rs536739208	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:885533	TTCAGAGACAGGAAG[A/G]GGCTGCGCTGTGGCC	10025
rs536804028	snp	A/G			intron-variant	MED16	GRCh38.p7	19:868607	CTCGCCGTCCCTCAC[A/G]CCTGCTCCCCACGTC	10025
rs536816473	snp	A/G			intron-variant	MED16	GRCh38.p7	19:884510	TCCGGAGGATTCCGT[A/G]CACCGCCCCTGCCCG	10025
rs536833977	snp	C/G	0.000399281	0.0141238	downstream-variant-500B	MED16	GRCh38.p7	19:867640	GCATGCAGAGACACA[C/G]AGACCATACACAGAG	10025
rs536858150	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:888439	TGAGGCAGGAGAATC[A/G]CTTGAACCCAGGAGG	10025
rs536881405	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:870742	CCGTATGGATTCGGG[A/G]GGGTCCTGGGGCAGG	10025
rs536974538	snp	G/T			upstream-variant-2KB, nc-transcript-variant	MED16, RNU6-9	GRCh38.p7	19:893540	CAGAGAAGATTAGCA[G/T]GGCCCCTGCGCAAGG	10025
rs536982069	in-del	-/A			intron-variant	MED16	GRCh38.p7	19:870567	CCTGTCGGGGAGACA[-/A]AAAAAAAAAAAAAAA	10025
rs537003626	snp	C/T			intron-variant	MED16	GRCh38.p7	19:883589	AAAGGCTGTGGCATG[C/T]GTGTGAGACGTGGCT	10025
rs537069011	snp	A/G	0	0	intron-variant	MED16	GRCh38.p7	19:887311	ACGTCTGTGTGGGTC[A/G]CAGGCTGGCATGTCT	10025
rs537107233	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:890540	TTTGCACCCCGATTT[A/G]ATTCCAATTTTCTGT	10025
rs537142685	snp	C/G	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:886860	GCAGGTGGATCCCCT[C/G]AGGTCAGCAGTTCAA	10025
rs537168959	snp	A/G	0.00438332	0.0466095	intron-variant	MED16	GRCh38.p7	19:868598	CTCCCTCTGCTCGCC[A/G]TCCCTCACGCCTGCT	10025
rs537175605	snp	A/G			intron-variant	MED16	GRCh38.p7	19:869507	TTACAAGCCTCTGAC[A/G]TAACCGTCCTCTCTT	10025
rs537179329	snp	A/G	9.6177e-05	0.00693392	missense, utr-variant-5-prime	MED16	GRCh38.p7	19:890190	TGCTCTGAGGGGATC[A/G]AGTGCAGGTCCCAGG	10025
rs537264667	snp	A/G/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:889985	CCTGAACAAGAATGA[A/G/T]TCGGGCCACTATGGA	10025
rs537292652	snp	A/G	0.000183896	0.00958718	intron-variant	MED16	GRCh38.p7	19:873613	GGTCGGGTCAGCTCG[A/G]GCCTCTTGTACACAC	10025
rs537331597	snp	C/T	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:876821	GCACTTTACTGACCA[C/T]GGGGCCCCTGCCTGC	10025
rs537363090	snp	G/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:873244	TGGGACTCCAAGTAG[G/T]GGTGGGACTCCAACC	10025
rs537424964	snp	A/C	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:870233	GAGGCTAAGGCAGGG[A/C]GCCCTGTACAGCGAG	10025
rs537467121	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:892806	TCGCCCCAAACTCTC[C/T]TTAGGCCCCGCCCCG	10025
rs537472612	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:888781	TGTACTGCGGCAATG[C/T]GCCGACAATGGCAGT	10025
rs537473382	snp	A/G	0.00199481	0.0315187	intron-variant	MED16	GRCh38.p7	19:872498	AGGGAGGCCCCAGGG[A/G]TGGCCCCTGGCAGCC	10025
rs537510701	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	MED16	GRCh38.p7	19:894860	AGGCTGAGGCACGCA[C/G]ATCACCTGAGAACAG	10025
rs537574028	snp	A/G	0.00199481	0.0315187	intron-variant	MED16	GRCh38.p7	19:876605	GCAGCTTTCCTGGAC[A/G]GGCCTCTGGGAGCAC	10025
rs537604557	snp	C/T	0.00478085	0.0486577	intron-variant	MED16	GRCh38.p7	19:874980	CCAGCCTGGCCAACA[C/T]GGTGAAACCCCGTCT	10025
rs537691025	snp	C/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:879657	AGCTCACGTTCCCCT[C/G]GTTGTCAATGCCCAC	10025
rs537692783	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:874734	AATTAAAAACCGGGT[A/G]TGGTGGCACGTGTCT	10025
rs537731026	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:878565	CCCACCAGCCCCAGC[C/T]CCAGCCCCACATGCC	10025
rs537731582	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:881340	ATATTAAAGAACACT[A/G]GATCTGTCTGCCAGC	10025
rs537823303	snp	A/C	0.000399281	0.0141238	downstream-variant-500B	MED16	GRCh38.p7	19:867908	GACACAGGCTCCCGG[A/C]ACCAAATCGAGGTCG	10025
rs537907114	snp	A/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:892005	GCGGGGCTGAGTGTG[A/T]CGGGGAACACCTGTG	10025
rs537936758	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:880228	CTCCTGCTCTGCAGG[A/G]TGTGGAGAGCCGGGG	10025
rs537964367	snp	C/T	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:872235	CAGGGTCTGGGACAT[C/T]TGTGGTGGTCAGGAC	10025
rs538012436	snp	A/G			intron-variant	MED16	GRCh38.p7	19:876929	GCCCCCACCTGCCAC[A/G]GGGCCCCCACCTGCC	10025
rs538059896	snp	G/T	0.000187992	0.00969332	synonymous-codon, utr-variant-5-prime	MED16	GRCh38.p7	19:886154	CAGCGTGAGCGACGG[G/T]GAGAACTTGACTCGG	10025
rs538199404	snp	A/G	0.152778	0.230321	intron-variant	MED16	GRCh38.p7	19:872947	GGAGGGCTCCGAGGT[A/G]GGGGAGGGCTCCGAG	10025
rs538404680	snp	A/G	0.000399281	0.0141238	synonymous-codon	MED16	GRCh38.p7	19:880060	ATCCACAGGCCTCGG[A/G]GCCGCGGAGCTGTAG	10025
rs538515272	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:884116	CCCACGTGCCCCCAC[A/G]TCTGGCCACTCCAGG	10025
rs538557263	snp	C/G	0.000111187	0.00745529	utr-variant-3-prime	MED16	GRCh38.p7	19:868068	GAGACGCCCGAGCCG[C/G]GTCACCACAAGGTCC	10025
rs538591965	snp	A/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:877514	TCCTAATACGTGCTG[A/T]GAGCCACCCCACTGA	10025
rs538679115	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:877369	ATGCACAATGCCTCT[A/G]GGAACAGGGAAGGAA	10025
rs538717500	snp	A/C/G	0.00017838	0.00944255	intron-variant	MED16	GRCh38.p7	19:877210	GCCCAAGGAGAGCCC[A/C/G]GTGAGATGGGGCTGC	10025
rs538760059	in-del	-/G	0.00279162	0.0372561	intron-variant	MED16	GRCh38.p7	19:881096	GGAAGAACGGGAGCT[-/G]GGGGGAAGAAAGGGC	10025
rs538792282	snp	C/T	0.0023933	0.0345097	intron-variant	MED16	GRCh38.p7	19:884736	GAATGCTGGCAGGCG[C/T]GCGGTCACACCCGAG	10025
rs538803524	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:881385	AAGATGAGATCTGCC[C/T]CCTAATTGGGAACCC	10025
rs538829046	snp	C/T	0.00159617	0.0282053	intron-variant	MED16	GRCh38.p7	19:887536	CCGGGCGCGGTGGTG[C/T]GTGCCTGTAATTCCA	10025
rs538830741	snp	A/G	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:869249	GTCGGTCCGCCACGT[A/G]CCCGGGGAGCCTGAG	10025
rs538994291	snp	A/C/G	0.000101778	0.00713302	intron-variant	MED16	GRCh38.p7	19:868504	CACAGCCGCACCTGC[A/C/G]GGGAGGCAGGCACTG	10025
rs538995493	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:882443	GAGGTAGGATTGCTC[A/G]AGCCCAGGAAGATGA	10025
rs539012230	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	MED16	GRCh38.p7	19:895132	GGTGGGGTGATGCAC[A/T]CCTGTAGGCCCAGTT	10025
rs539032556	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:885282	CAAGGAGTTTGGGGC[A/G]TTACTGATTCCTAAT	10025
rs539065477	snp	G/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:886482	CACCTCCCCTTTCTG[G/T]AAAGGGACAGACAGC	10025
rs539133427	snp	C/T	0.00318978	0.0398085	intron-variant	MED16	GRCh38.p7	19:888350	AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAA	10025
rs539133488	snp	C/G	0.0115144	0.0749975	upstream-variant-2KB	MED16	GRCh38.p7	19:894753	AACATAGCCAGACCC[C/G]GTCTCTACAAAAAAA	10025
rs539234683	snp	C/T	0.00636936	0.0560724	intron-variant	MED16	GRCh38.p7	19:870558	AGAGTGAGACCCTGT[C/T]GGGGAGACAAAAAAA	10025
rs539250559	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:871738	CGGGGGGCTCAGGCA[A/G]GACTTGTGTTTTGGT	10025
rs539260775	snp	C/T	0.00020029	0.0100053	missense, utr-variant-5-prime	MED16	GRCh38.p7	19:891115	CCACCTGCCGCTGGC[C/T]GCCGCAAATCACACA	10025
rs539283288	snp	C/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:872917	AGGCTTCTTACAGCA[C/G]AGGCTTCATGGAGAG	10025
rs539295109	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:870388	CAACATTGCAAAACC[A/G]CCTCTATACCAAAAA	10025
rs539298629	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:890854	GGGCCAGGGTGAGTG[A/G]GAGGTGGCCTGAGAG	10025
rs539334916	snp	C/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:874382	CTCCCAAAGTGCTGG[C/G]ATTACACACGAGTCG	10025
rs539365876	snp	C/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:875759	CGGGTGGAGGCTGGG[C/G]AGGCTGCTCAACAGG	10025
rs539472789	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	MED16	GRCh38.p7	19:894223	GTATTTTTAGTAGAG[A/G]CGGAGTTTCACCATG	10025
rs539478412	snp	C/T	0.000798403	0.0199641	missense	MED16	GRCh38.p7	19:871047	CGCACCTGGCGAGGC[C/T]GTCGAGCTGCAGGGT	10025
rs539509720	snp	C/G/T	0.000399281	0.0141238	upstream-variant-2KB, downstream-variant-500B	MED16, RNU6-9	GRCh38.p7	19:893722	CCTGCCTCAGCCTCC[C/G/T]GAGTAGCTGGGATTA	10025
rs539510209	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:886237	GAGGAGGGGCCGCTC[A/G]GGCTCATGGGGGCTG	10025
rs539700107	snp	C/T	0.00016919	0.00919601	intron-variant	MED16	GRCh38.p7	19:890294	ACCACAGCCTGCAGA[C/T]GATGACGATGACTCC	10025
rs539724442	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:880646	GCTGCAAAGCCGGGC[A/G]CGGTGGCTCACGCCT	10025
rs539789829	snp	A/G			upstream-variant-2KB, nc-transcript-variant	MED16, RNU6-9	GRCh38.p7	19:893548	ATTAGCATGGCCCCT[A/G]CGCAAGGATGACACG	10025
rs539826611	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:868647	CACAGGGCCTCTGCC[C/T]ATGCTTCTCCTCCCC	10025
rs539890592	snp	A/G	0.000333021	0.0128996	intron-variant	MED16	GRCh38.p7	19:891181	TGGTGGGACGTCTAT[A/G]TTGGCTGAGCACCCA	10025
rs539901035	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:887776	AGACACAGAAGGCTA[C/T]GCAGTGTGTGATCCT	10025
rs539940388	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:891457	GCCAAGGGCACAGCC[A/G]GGAGACGCAGCGGAG	10025
rs539978173	snp	C/T	0.00010741	0.0073276	intron-variant	MED16	GRCh38.p7	19:890931	GGGACACCATGCGGC[C/T]GGGAGGGGAAGCAGG	10025
rs540135237	snp	C/T	0.00318978	0.0398085	intron-variant	MED16	GRCh38.p7	19:873974	CCGGCTGGCAGCTGG[C/T]GGCGGTTACACACCC	10025
rs540205616	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:869849	TGAAACAGGCTGGGG[A/G]TCTGACGGGCCTGGG	10025
rs540215536	snp	C/G	0.00159617	0.0282053	intron-variant	MED16	GRCh38.p7	19:872305	GCTGCTCAGAGCCCT[C/G]CAGGGCCCAGGACAG	10025
rs540278770	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:869355	CTGCCCAGACACCCG[A/G]CCTGGAGGTGCCGGG	10025
rs540310761	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:875127	TGAGATCGCACCACT[A/G]CACTCCAGCCTGGGC	10025
rs540340037	snp	C/T	0.00478085	0.0486577	intron-variant	MED16	GRCh38.p7	19:869135	GCCCAGTAAAGGGGG[C/T]GGGACCCCCCACACG	10025
rs540434914	snp	C/T			intron-variant	MED16	GRCh38.p7	19:875008	TCTCTACTAAAAATA[C/T]AAAAAATCAGCCGGG	10025
rs540512365	snp	G/T			intron-variant	MED16	GRCh38.p7	19:883742	CGGGGGCACCGGGCA[G/T]TGAAGGTGCAGGTCT	10025
rs540576962	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:870917	GGCGGGGAGCCGTGT[A/G]GATTCGGGGGGACCT	10025
rs540619012	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:891533	CACTAGCTCTCTCCC[A/G]AAGGAAGAGCCCGCA	10025
rs540664541	snp	A/G	1.69355e-05	0.00290989	missense	MED16	GRCh38.p7	19:872016	CGGGCAGGCAGCTGG[A/G]CTTCAGAAGGCCCCA	10025
rs540745566	snp	A/G	0.00478085	0.0486577	intron-variant	MED16	GRCh38.p7	19:876539	CCTGTGGGGCTTAAC[A/G]TGTTACAGAAGAAAC	10025
rs540832866	snp	C/T	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:877870	CATGCCCCAGCAGCT[C/T]GCCTTCCCCTGGTTG	10025
rs540896512	snp	A/G			intron-variant	MED16	GRCh38.p7	19:876302	CCACACCACTGCAAG[A/G]GACCCTTCTGGCACG	10025
rs540947781	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:885083	CGGAGCCTGAGCTGC[A/G]GGACCCTGGGGCCAC	10025
rs540972176	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:873656	CTGCACCCCTCGGTC[C/T]TTCGACCTGCACTGA	10025
rs540982672	snp	C/G/T	0.000196367	0.00990682	intron-variant	MED16	GRCh38.p7	19:868857	GCGGTTCCGGGGGCC[C/G/T]CTCACCTGGTGCAGG	10025
rs540989652	snp	A/G	1.77577e-05	0.00297969	intron-variant	MED16	GRCh38.p7	19:881766	GAGTAAAGACAGGCT[A/G]AGACAGCCGCAGGAG	10025
rs541004176	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	MED16, RNU6-9	GRCh38.p7	19:893554	ATGGCCCCTGCGCAA[A/G]GATGACACGCAAATT	10025
rs541034184	snp	A/G	0.00597247	0.0543191	intron-variant	MED16	GRCh38.p7	19:877304	CACGCCCGTGTGTGG[A/G]CCTGTGTGCGCGCAT	10025
rs541062003	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:876863	CCCCACCTGGCACGG[A/G]ACCACCTGCCACGGG	10025
rs541114387	snp	C/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:884625	GTCCCCGCTGGCTGA[C/G]CAACGACACCTCTCA	10025
rs541153095	snp	C/T	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:884234	CAGGCCCGCAGCCTC[C/T]GAGGCTCTGAAAACC	10025
rs541190590	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:880778	TACAAAAAATTAGCC[A/G]GGCGTGGCAGCACGC	10025
rs541220728	snp	G/T	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:880512	GGCATCTTAGGGTGG[G/T]GGGCTGGGGCTGTCA	10025
rs541259049	snp	A/G			intron-variant	MED16	GRCh38.p7	19:882838	GTCTCTGCCCCGGAC[A/G]GGCCATCACGGTCAC	10025
rs541275854	snp	C/T	0.00398564	0.0444627	intron-variant	MED16	GRCh38.p7	19:868737	GGATCCTGGCTCCAA[C/T]ACTCCCTCTGGGACG	10025
rs541315655	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:890352	GTCCCACCCCAGGAA[A/G]GTCACAGAACTGCTG	10025
rs541367199	snp	C/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:886342	CTGACTCGGCCACCT[C/G]AGCCGTGTGGGATGT	10025
rs541426833	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:882877	GACCTCCTGCAAACC[C/T]GTATAGGGGTCCTGT	10025
rs541515071	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:885650	CCCCGGGAGGGACCG[A/G]CCCTGCCCACACCAC	10025
rs541529522	snp	C/G			intron-variant	MED16	GRCh38.p7	19:873005	GGCTCCGAGGTGGGG[C/G]AGGGCTCCGAGGTGG	10025
rs541554340	snp	G/T	0.0162398	0.0886349	intron-variant	MED16	GRCh38.p7	19:885462	GCACGTTGGGGGGGG[G/T]CCGGGGGCCCCAGTG	10025
rs541562924	snp	C/G	0.000399281	0.0141238	downstream-variant-500B	MED16	GRCh38.p7	19:867960	ACGGCAGGGACGCGG[C/G]CCTGGGCGCAGAGGG	10025
rs541588512	snp	A/G	0.0023933	0.0345097	intron-variant	MED16	GRCh38.p7	19:885698	CCCGCGCGGGTCTCC[A/G]CCCCCAGGACCCTGA	10025
rs541624260	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:870104	CCCCGGGAGATCCTC[C/T]TGATGAGGTGTCTGC	10025
rs541627760	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:890577	CTAGTTTTCTCTAAT[A/G]ACCACGTATTATGAG	10025
rs541675290	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:892069	TGTGGCCGAGGCGGG[C/G]GCTGAGTGTCACAGG	10025
rs541707898	snp	C/G	8.52057e-05	0.00652653	synonymous-codon	MED16	GRCh38.p7	19:871990	CTGGGTATCCGAGGT[C/G]GCCGTATACACGGGC	10025
rs541756444	snp	G/T			intron-variant	MED16	GRCh38.p7	19:870179	ACAGAGGGATCTACG[G/T]CGAGGCCTGACATCC	10025
rs541786462	snp	C/G	0.0023933	0.0345097	upstream-variant-2KB, downstream-variant-500B	MED16, RNU6-9	GRCh38.p7	19:893853	GCCCGCCTCGGCCTC[C/G]CAGAGTACTGGGATT	10025
rs541807219	in-del	-/C	0.00390719	0.0440264	intron-variant	MED16	GRCh38.p7	19:889054	TACTCTTAACTGTCC[-/C]CCCCAACCCTGGCCA	10025
rs541821935	snp	A/G	3.38404e-05	0.00411328	intron-variant	MED16	GRCh38.p7	19:868283	GGTTAACCGCGCCGA[A/G]GAGAGTCCAGGGCGA	10025
rs541875221	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:889822	CCTGAGGGCAAGAAG[C/T]CATCATTGCGAACCT	10025
rs542033613	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:869801	AATCAGTGGCTCAGA[A/G]GGTTTGCATGTGCTC	10025
rs542095965	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:875556	TGACACCAGGCGCTC[A/G]GTCAGCTGGGCAAGC	10025
rs542190033	snp	C/T			intron-variant	MED16	GRCh38.p7	19:885555	GCTGTGGCCACGAAG[C/T]GGGAGGAAGGCGCCC	10025
rs542257403	snp	A/G	0.00025937	0.011385	missense	MED16	GRCh38.p7	19:868171	TGGTGTGTGGACTGC[A/G]GGCCCAGCTGGACAA	10025
rs542268408	in-del	-/AAC			intron-variant	MED16	GRCh38.p7	19:887098	AACAAAAAAAAAAAG[-/AAC]AAGAAAAATGTCTCT	10025
rs542284590	snp	C/G	0.000107095	0.00731683	intron-variant	MED16	GRCh38.p7	19:868971	GAGGGGAGAACGTGA[C/G]GGAGGCCTGGGCACC	10025
rs542293230	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:870615	AAGGGCTGGGTGCCC[A/G]TGTTGGGGGTGGTTC	10025
rs542329897	snp	C/G	0.00199481	0.0315187	intron-variant	MED16	GRCh38.p7	19:873061	CTCCGAGGTGGGGCA[C/G]GGCTCCGAGGTGGGG	10025
rs542349426	snp	A/C	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:893116	GCCAAGCTCAGCGGG[A/C]GTCCGCGGTGCGATC	10025
rs542354621	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:870455	AATCCCAGCTACTGG[A/G]AAGGCTGAGGTAGGA	10025
rs542393052	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:872769	CAGGCGCAGGGAGCT[A/G]GGGAGGGTAAGGGGT	10025
rs542394626	snp	A/G	0.000186919	0.00966565	utr-variant-3-prime	MED16	GRCh38.p7	19:868058	GGAAACCGAGGAGAC[A/G]CCCGAGCCGGGTCAC	10025
rs542532266	snp	C/T			intron-variant	MED16	GRCh38.p7	19:887358	AGCACATGTGCCTTT[C/T]ATTAATGTAATTAAA	10025
rs542586262	snp	A/G	0.00159617	0.0282053	intron-variant	MED16	GRCh38.p7	19:874744	CGGGTGTGGTGGCAC[A/G]TGTCTGTAATCCCAG	10025
rs542586349	snp	A/C	0.00636936	0.0560724	intron-variant	MED16	GRCh38.p7	19:871806	GGGGAGAAGGGAGAG[A/C]GGGGAGAGGGGAGAG	10025
rs542591499	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:881249	CTGCAGCACAGAGAG[A/G]ACACATGCCGCCTAC	10025
rs542623228	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:874555	CCTCAGTCCCCTTAC[A/G]GCAAAACGGAAGGAG	10025
rs542666972	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:878637	ACAACCCCAGCCCCA[C/T]GTGCCCCAGCAGCTC	10025
rs542817737	snp	C/T	0.000190585	0.00975993	intron-variant	MED16	GRCh38.p7	19:877229	AGATGGGGCTGCGCC[C/T]TCAGCCGGGAGAGGA	10025
rs542855231	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:881817	AACCTGCCCAGGGCC[C/T]TTCCCAGGTCTCATG	10025
rs542987230	snp	A/G	0.00517822	0.0506191	intron-variant	MED16	GRCh38.p7	19:873109	GGAGGGCTCCGAGGT[A/G]GGGCAGGGCTCCGAG	10025
rs542987261	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:876486	CTCCAGACTGGGAAC[A/G]CTGGAGAGGGGAGCC	10025
rs543102136	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:869682	GTGCCTTCCCTGGAG[A/G]TCCTGGAGCCGAGCC	10025
rs543105974	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:877719	TGCCCACCAGCCCCT[A/G]CCCCACGTGCCCCAG	10025
rs543142711	snp	G/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:882129	ATGGTCGCACCCACA[G/T]ATCCGCTGCCTGACA	10025
rs543157056	snp	A/G			intron-variant	MED16	GRCh38.p7	19:888911	GACGCACAGAGGCAC[A/G]AAGCTGGGGTGGCTG	10025
rs543186060	snp	G/T	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:883530	GATGGGTGCGGTGGG[G/T]ACTGTCCCAGTGACC	10025
rs543334881	snp	C/T	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:884861	AAAACCAACCGCCCC[C/T]GAGGGCAGGCCCAGG	10025
rs543371471	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:887755	TCACGCTCAGTAAGA[A/G]ATGCCAGACACAGAA	10025
rs543418603	snp	A/G	0.00318978	0.0398085	intron-variant	MED16	GRCh38.p7	19:880691	TTGGGAGGCTGAGGC[A/G]GGCAGATTGCCTGAG	10025
rs543433916	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:884175	GTGCTCTCATCTACC[A/G]GGAAAACATCTCCCT	10025
rs543527869	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:870288	AAGGCAAGGCCGGGG[C/T]GGTGGCTCACACCTG	10025
rs543545764	snp	A/G	6.89406e-05	0.00587073	missense	MED16	GRCh38.p7	19:885960	CTGCTGCCGTCCGCC[A/G]TGGCCACCACGATGT	10025
rs543620095	snp	A/G/T	0.000153888	0.00877053	intron-variant	MED16	GRCh38.p7	19:868524	GGCAGGCACTGAGCG[A/G/T]GTTCCCACTTCCAGG	10025
rs543661804	snp	A/C	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:886286	CACGCGCACAGAAGA[A/C]CCACGCAGAAGCCAG	10025
rs543693287	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:873387	CAGGGGCAGGGAAGC[A/G]GGGTCCTGATGAGAT	10025
rs543704942	snp	C/T	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:870891	TCGGGGGGTCCCGGG[C/T]AGGACATGGAGGCGG	10025
rs543783255	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:889370	AACTCACTAAGAACG[A/G]CCACCCTCAGTTAAA	10025
rs543862190	snp	A/G	0.00199481	0.0315187	intron-variant	MED16	GRCh38.p7	19:888582	GGTGGTGGCCGCACA[A/G]CATGGCGAGTGTATA	10025
rs543900851	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:868684	ATGCTGCTCCCTGAA[C/T]TAGCCCCGCCACACC	10025
rs543941005	snp	A/C	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:890317	ATGACTCCAGGCAGG[A/C]TCCAGGTAAGCCGGT	10025
rs543946402	snp	C/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:888177	CCACTACACTCCAGC[C/G]TGGGCAACAGAGCAA	10025
rs543948341	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:891469	GCCGGGAGACGCAGC[A/G]GAGGGTCTGCGCTGG	10025
rs543976337	snp	C/T			upstream-variant-2KB	MED16	GRCh38.p7	19:894121	GCTCACTGCAACCTC[C/T]GCCTTCCAGGCTCAA	10025
rs543977760	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, downstream-variant-500B	MED16, RNU6-9	GRCh38.p7	19:893809	GCCATGTTGGCCAGG[A/G]TGGTCTCTATCTACT	10025
rs543978340	snp	C/T	0.00755907	0.0610114	intron-variant	MED16	GRCh38.p7	19:869734	CTGCTGGAGGTTCAC[C/T]TCATTTTCTTCCTTT	10025
rs543987096	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:891232	CAGAAGTGGGAAAAC[A/G]ATGGAGGCCCGTGGT	10025
rs544161482	snp	A/T	5.76175e-05	0.00536707	intron-variant	MED16	GRCh38.p7	19:871696	TCAAGGCAGAGCCAC[A/T]GCCACCTGCAGGGGC	10025
rs544170296	in-del	-/TATTTT	0.00199481	0.0315187	upstream-variant-2KB, downstream-variant-500B	MED16, RNU6-9	GRCh38.p7	19:894032	GATGTGGTGCTCTTC[-/TATTTT]TATTTTTATTTTTTT	10025
rs544214164	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:885454	ACGGGAGAGCACGTT[A/G]GGGGGGGTCCGGGGG	10025
rs544279742	in-del	-/CCC	0.0533365	0.154349	intron-variant	MED16	GRCh38.p7	19:889052	CCTACTCTTAACTGT[-/CCC]CCCCAACCCTGGCCA	10025
rs544375265	snp	C/G/T	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:870433	AGGTGTGGTGGCTCA[C/G/T]GCCTGTAATCCCAGC	10025
rs544439893	snp	A/G	0.00398564	0.0444627	intron-variant	MED16	GRCh38.p7	19:871782	CGGGGAGAGGGGAGA[A/G]GGGAGAGCGGGGAGA	10025
rs544615267	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:885576	GAAGGCGCCCCGAAC[C/T]GAGGGATTGGGCGCC	10025
rs544623624	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:870178	CACAGAGGGATCTAC[A/G]GCGAGGCCTGACATC	10025
rs544662494	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:892420	CGCCCTTAGCTCTCC[A/G]GGCCCAACCCCTAAA	10025
rs544723249	snp	A/G	0.000279759	0.0118238	synonymous-codon	MED16	GRCh38.p7	19:871144	GCGGCTAACCAGGCC[A/G]TCGCTGGCTGGCAGC	10025
rs544770223	snp	A/T			intron-variant	MED16	GRCh38.p7	19:875176	CTCAAAAGAGTAAAA[A/T]AAATAAATAAAAATA	10025
rs544827966	snp	G/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:879922	GCCCCGGCCCCACGT[G/T]CCCCAGCAGCTCACC	10025
rs544926403	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:882596	CTGCATGTGGGACAC[A/G]GAGGGCAGCTGGAGC	10025
rs544944778	snp	C/T	0.00079952	0.019978	intron-variant	MED16	GRCh38.p7	19:871428	CCCCGGCTCTGCCTG[C/T]CTGGCTGGGTGACCC	10025
rs544973788	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:874313	GAGACGGGGTTTCAC[C/T]GTGTTAGCCAGGATG	10025
rs544973856	snp	A/C	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:877658	CAGCCCCAGCCCCAG[A/C]CCCAGACCCACGTGC	10025
rs544975126	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	MED16	GRCh38.p7	19:894562	GTGTTTTTTCTGGAT[C/T]AGGGTTCAGTTCTCC	10025
rs545004768	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:890378	TGCTGTCAGCCGAGT[C/T]GACAGCTCAGGGAAC	10025
rs545031852	snp	C/T	0.00159617	0.0282053	intron-variant	MED16	GRCh38.p7	19:873894	CTGGTGCACATCTGC[C/T]CCCTGCTCCGAGGTG	10025
rs545081100	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:882110	TCCAATAAAGCCATG[C/T]GGGATGGTCGCACCC	10025
rs545285156	snp	A/G	0.00398564	0.0444627	intron-variant	MED16	GRCh38.p7	19:884168	AATGCCTGTGCTCTC[A/G]TCTACCGGGAAAACA	10025
rs545296864	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:884679	GGCAGCCGCCGCAGC[A/G]GGCGTGGAAGGATGG	10025
rs545302001	snp	A/G	0.000101786	0.00713322	intron-variant	MED16	GRCh38.p7	19:868960	CCCTGGCGGGAGAGG[A/G]GAGAACGTGAGGGAG	10025
rs545399512	snp	C/G/T	4.05986e-05	0.00450533	missense	MED16	GRCh38.p7	19:880125	CGATGTGGACGCTGC[C/G/T]GTCGTGGAAGGCCAG	10025
rs545479656	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:881784	ACAGCCGCAGGAGTC[C/T]AGCATGGCCTGGTGT	10025
rs545484403	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:883132	TGACGGCTGCGGTCA[A/G]CATTCCTAAATGAGG	10025
rs545520286	snp	A/G	0.0023933	0.0345097	intron-variant	MED16	GRCh38.p7	19:884791	GCGAGACGATCGCTT[A/G]GGGCCGGGGTTCAGG	10025
rs545533698	snp	A/G	0.00279162	0.0372561	intron-variant	MED16	GRCh38.p7	19:882431	ACTCAGGAGGCTGAG[A/G]TAGGATTGCTCGAGC	10025
rs545538885	in-del	-/GGAGGGCTCCGAGGTGGG	0.00716266	0.059414	intron-variant	MED16	GRCh38.p7	19:872932	GAGGCTTCATGGAGA[-/GGAGGGCTCCGAGGTGGG]GGAGGGCTCCGAGGT	10025
rs545678770	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:887409	GCGGTGGCTCACGCC[C/T]GTAATCTCAGCACTT	10025
rs545751245	snp	A/C	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:875585	GCTGCTTCGCCTCTG[A/C]ACCTCAGCAACCTCA	10025
rs545763009	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:890612	TATTACTCAAACAAT[A/G]GAGAGAAGACGGGCA	10025
rs545900546	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:886676	CAGGAAGTGCTGTGT[A/G]AGCACCAGCGGCTGC	10025
rs546001833	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:885685	TAGCCCGTGGAGGCC[C/T]GCGCGGGTCTCCACC	10025
rs546038895	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:888899	CCAGCACAAGCAGAC[A/G]CACAGAGGCACGAAG	10025
rs546124016	snp	G/T	0.021333	0.101051	intron-variant	MED16	GRCh38.p7	19:873072	GGCAGGGCTCCGAGG[G/T]GGGGGAGGGCTCCGA	10025
rs546168063	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:892212	TCCTCAAACCCTAAC[C/G]CCGGCTCCCTACTTC	10025
rs546216327	snp	A/C			intron-variant	MED16	GRCh38.p7	19:887938	CTGGGCACAGTGACT[A/C]ACGCCTGTCATCCCA	10025
rs546277765	snp	C/G			intron-variant	MED16	GRCh38.p7	19:889344	GGACAGTAGCCTCCA[C/G]TGAAAGAGATAACTC	10025
rs546327323	snp	C/G	3.35126e-05	0.00409331	intron-variant	MED16	GRCh38.p7	19:868299	GAGAGTCCAGGGCGA[C/G]CGGTGGCTCTTGCAG	10025
rs546364758	snp	G/T			intron-variant	MED16	GRCh38.p7	19:872164	GCGGCGGGGGGCAGA[G/T]GGCGATGGGATGAAG	10025
rs546463061	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:887231	AGGTCCAGAAGTCCA[A/G]GAAGCAAGCCAGGCC	10025
rs546500778	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	MED16	GRCh38.p7	19:894179	TAGCTGGGACTACAG[A/G]CGCGCACCACCATGC	10025
rs546500822	snp	A/G			intron-variant	MED16	GRCh38.p7	19:876385	GTTCATCTTCTGACC[A/G]TGTTTGCTGAGGCCT	10025
rs546552842	snp	C/T	0.00456619	0.047563	intron-variant	MED16	GRCh38.p7	19:890460	TCTTTAAAACCAGAT[C/T]AGAAGAAAATGACTC	10025
rs546561765	snp	A/G	0.000798403	0.0199641	downstream-variant-500B	MED16	GRCh38.p7	19:867581	CAGCAGAGAGCAGCT[A/G]GAGAAACATAACAGG	10025
rs546607840	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:872845	GGTGGGGCTGAGAAG[A/G]AGCAGGGCCTGGGAG	10025
rs546684470	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:869230	GGCCCACACAGGGAC[A/G]AGGGTCGGTCCGCCA	10025
rs546722956	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:887494	AAGATAGTGAAACCC[C/T]GTCTCTACTAAAAAT	10025
rs546759068	snp	A/G	0.0182019	0.0936463	intron-variant	MED16	GRCh38.p7	19:871830	GGGAGAGCGGGGAGA[A/G]GGGAGAGCGGGGAGA	10025
rs546847164	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:874573	AAAACGGAAGGAGGA[A/G]CAGACCTGCCTGCAC	10025
rs546850353	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:868843	ATCTCTGGGAGTCAG[C/T]GGTTCCGGGGGCCCC	10025
rs546858121	snp	C/T	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:871502	TTCACTTAAAAAGTA[C/T]GTGGGAAGCACTGTG	10025
rs546895377	snp	A/C/T	0.000129074	0.00803245	synonymous-codon	MED16	GRCh38.p7	19:871216	GCATTCATCCACCAG[A/C/T]GCCTCGTCCGGCTCG	10025
rs546957119	snp	A/C	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:888333	TCGAGACCAGCCTGG[A/C]CAACATGGTGAAACC	10025
rs547067312	snp	A/G	0.00199481	0.0315187	intron-variant	MED16	GRCh38.p7	19:873199	GCAGGGCTAGGAAGT[A/G]GGGGTTTAAGAAGAG	10025
rs547089098	snp	C/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:891317	CCGAGGGGGAACATG[C/G]AGAGGTCAGGGCCAG	10025
rs547125995	snp	A/G	5.00054e-05	0.00500002	missense, utr-variant-5-prime	MED16	GRCh38.p7	19:891109	ATCATCCCACCTGCC[A/G]CTGGCCGCCGCAAAT	10025
rs547132100	snp	C/T			intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:892006	CGGGGCTGAGTGTGA[C/T]GGGGAACACCTGTGG	10025
rs547176797	snp	A/G	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:874348	CGATCTCCTGACCTC[A/G]TGATCAGCCCGCGTT	10025
rs547278532	snp	A/G	0.00159617	0.0282053	intron-variant	MED16	GRCh38.p7	19:875745	CCCCTGCCAAGTAAC[A/G]GGTGGAGGCTGGGGA	10025
rs547345888	snp	C/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:881856	CTCCCATGCCCAGAA[C/G]ACCAGGCCCGGCCAA	10025
rs547477839	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:893470	TAAATAGCTGGTGGT[A/G]GAACTCAATATTCGT	10025
rs547478584	snp	A/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:881308	GGCTCCCTTGTTGAT[A/T]TGCAATGACTCTTTA	10025
rs547564935	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:876671	GCCCCTCTTGCCCTC[C/T]GCCTGCCATAGAGCC	10025
rs547734955	snp	A/C	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:873771	GAGCCCACTGCCTGC[A/C]CCCCCCCGGGGGCCG	10025
rs547737105	snp	A/T			intron-variant	MED16	GRCh38.p7	19:884244	GCCTCCGAGGCTCTG[A/T]AAACCAAGCGGCTGT	10025
rs547842833	snp	C/T	0.00199481	0.0315187	intron-variant	MED16	GRCh38.p7	19:874900	TGTAATCCCAGCCTT[C/T]AGGCTATATCCCAGC	10025
rs547907800	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:882317	GTTCAAGACCAGCCT[A/G]GACAACACAGCAAGA	10025
rs547976298	snp	C/T			intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:892138	TGGCATCCAGACGGG[C/T]TGTTTCGCTTCGCAA	10025
rs548001227	snp	C/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:885173	CCAGGCCTGTCCCCA[C/G]AGCCCAACATCCACT	10025
rs548021583	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:886753	ACATACGGAAACATC[C/T]ACCCTTCTTTCAACG	10025
rs548107032	snp	A/G	0.000104499	0.00722761	intron-variant	MED16	GRCh38.p7	19:890130	CCACGTGGGACCAGC[A/G]CCTCACCTGACTGGT	10025
rs548110415	snp	C/G	0.000399281	0.0141238	downstream-variant-500B	MED16	GRCh38.p7	19:867550	CAGAAACTTGGCCCA[C/G]GGGCTAAGCAACCTC	10025
rs548130074	in-del	-/C	0.0597027	0.162132	intron-variant	MED16	GRCh38.p7	19:889154	TACTCTTAACTGTCC[-/C]CCCCAACCCTGGCCA	10025
rs548139133	snp	C/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:888245	ATAAAGGTCTGGCCG[C/G]GCTCGTTGGCTCACA	10025
rs548228551	snp	C/T	0.00159617	0.0282053	intron-variant	MED16	GRCh38.p7	19:891256	CCGTGGTAGAGGGAA[C/T]AGCCGATGCAAAGGC	10025
rs548256830	snp	C/G	0.00159617	0.0282053	intron-variant	MED16	GRCh38.p7	19:878104	CAGCCCCAGCGCCAC[C/G]TGCCCCAGCAACTCA	10025
rs548404885	snp	A/G	0.000130581	0.0080792	utr-variant-3-prime	MED16	GRCh38.p7	19:868050	TGAGGCAAGGAAACC[A/G]AGGAGACGCCCGAGC	10025
rs548431350	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:889102	CCCCAACCCTGGCCA[C/T]GCCTACTTCTTAACT	10025
rs548654286	snp	C/G	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:885714	CCCCCAGGACCCTGA[C/G]AAGCAGTGCTTCATT	10025
rs548741796	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:888751	GGGCCCCCGTGGCAC[A/G]AAGCCGGTGCTGCGT	10025
rs548829741	snp	C/T			intron-variant	MED16	GRCh38.p7	19:886290	CGCACAGAAGAACCA[C/T]GCAGAAGCCAGGAGT	10025
rs548835919	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:869899	ACTTCCTGACCGCGT[A/G]ACCCCAGATGAGTGG	10025
rs548838191	snp	A/G	0.00159617	0.0282053	intron-variant	MED16	GRCh38.p7	19:872404	TATCCCCACCTGCAC[A/G]TGGAGGAGCAGCCGC	10025
rs548876994	snp	A/C/G	7.82524e-05	0.00625467	intron-variant	MED16	GRCh38.p7	19:872143	AGAGGCATCGGTGTG[A/C/G]CTGGGGCGGCGGGGG	10025
rs548921180	snp	C/G	0.00438332	0.0466095	intron-variant	MED16	GRCh38.p7	19:871744	GCTCAGGCAGGACTT[C/G]TGTTTTGGTAGGGAG	10025
rs548972009	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, downstream-variant-500B	MED16, RNU6-9	GRCh38.p7	19:893623	CCCTCCCAGAAACGG[A/G]ATCTTGCTCTGTTGC	10025
rs548973261	snp	A/G			intron-variant	MED16	GRCh38.p7	19:875825	GTCTGTGGTGCCTAC[A/G]GGGAGACCCTGGTCT	10025
rs549003738	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:871721	AGGGGCTTATGTTCT[A/G]GCGGGGGGCTCAGGC	10025
rs549015357	snp	A/C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:887447	CCGAGGCGGGCAGAT[A/C/T]TCAAGGTCAGGAGTT	10025
rs549017182	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:884357	TGGCTCCGTGGGTGC[A/G]GGGGGCCCATCGGGC	10025
rs549042234	snp	C/T	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:874333	TAGCCAGGATGATCT[C/T]GATCTCCTGACCTCG	10025
rs549051147	snp	C/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:868797	AGCGCTGGGTGGGGG[C/G]TAGAATCAGCTGAGC	10025
rs549054338	snp	C/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:887173	TCGTACGGCTCCATT[C/G]TAAGTTACAAGTTAA	10025
rs549141369	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	MED16	GRCh38.p7	19:894160	CCTGCCTCAGCCTCC[C/G]GAGTAGCTGGGACTA	10025
rs549212388	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	MED16	GRCh38.p7	19:894882	TGAGAACAGGAGTTC[C/G]AGACTAGCCTGGCCA	10025
rs549225863	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:893479	GGTGGTGGAACTCAA[C/T]ATTCGTGCTCGCTTC	10025
rs549275659	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:877460	TGAGGAGTCTACCCC[A/G]TGAAAGGCGGTCCTC	10025
rs549333559	snp	C/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:869171	GGGTTGGTCTCCCAG[C/G]TGCCTGGGGAGCTTG	10025
rs549334048	snp	A/C	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:876623	CCTCTGGGAGCACAC[A/C]CCACACGCAGCCTCA	10025
rs549335827	snp	A/G	0.000399281	0.0141238	synonymous-codon, utr-variant-5-prime	MED16	GRCh38.p7	19:891045	GGGCACCGATGGGCA[A/G]TGGGTGCTCTTGGAC	10025
rs549436953	snp	G/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:881341	TATTAAAGAACACTG[G/T]ATCTGTCTGCCAGCC	10025
rs549462836	snp	A/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:875641	GCGCACAGGACCAGG[A/T]GCTGGGTTCTCAGCT	10025
rs549464856	snp	A/G	0.00755907	0.0610114	intron-variant	MED16	GRCh38.p7	19:872501	GAGGCCCCAGGGGTG[A/G]CCCCTGGCAGCCTAA	10025
rs549491963	snp	A/G	0.00159617	0.0282053	utr-variant-5-prime, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:893188	AACAACCAGTCGCCT[A/G]AGGCGTGGGGCCGCC	10025
rs549556529	snp	C/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:877329	GCGCATGTGTCTGTA[C/G]CGTCTGTACCTTTCT	10025
rs549727214	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:884693	CGGGCGTGGAAGGAT[A/G]GAGGAGTCTATACGC	10025
rs549777133	in-del	-/AAATAA	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:875181	AAGAGTAAAAAAAAT[-/AAATAA]AAATAAAATAAATAG	10025
rs549814171	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:892810	CCCAAACTCTCCTTA[A/G]GCCCCGCCCCGAACC	10025
rs550010986	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:879761	GTTGTCAATGCCCAC[C/T]AGCCCCAGCCCCACG	10025
rs550014903	snp	A/G	2.4052e-05	0.00346777	missense, utr-variant-5-prime	MED16	GRCh38.p7	19:886185	GAGAACTTCTCCCCG[A/G]AGCTGGAGGCGCCCG	10025
rs550170812	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:880814	TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG	10025
rs550201621	snp	C/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:876236	CAGCTGCCGGCTGAG[C/G]TCGTTAGATCTGAGG	10025
rs550389094	snp	C/T	0.0023933	0.0345097	intron-variant	MED16	GRCh38.p7	19:882410	CACACGCCTGTAGTC[C/T]CAGCTACTCAGGAGG	10025
rs550402819	snp	A/G	0.000112416	0.00749637	intron-variant	MED16	GRCh38.p7	19:871660	ATGGACCTGTGCTAG[A/G]AACTGGGGAAATAGC	10025
rs550431867	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:887537	CGGGCGCGGTGGTGC[A/G]TGCCTGTAATTCCAG	10025
rs550485720	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:884738	ATGCTGGCAGGCGCG[C/T]GGTCACACCCGAGAT	10025
rs550494903	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:893448	CAGACATTTGTTCCA[C/G]GGGCTTTAAATAGCT	10025
rs550526504	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	MED16	GRCh38.p7	19:868003	CTGTCCTTCCCAGCC[A/G]CTGCTTGTCCAGGTT	10025
rs550589866	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	MED16	GRCh38.p7	19:867825	CCACTGCTCACTTTG[A/G]ATACCCCCAGACTCG	10025
rs550611249	snp	A/C	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:881869	AAGACCAGGCCCGGC[A/C]AATCCGAGCGCTTCG	10025
rs550650901	snp	C/G	0.000399281	0.0141238	downstream-variant-500B	MED16	GRCh38.p7	19:867613	ACAGAGTCAGGCAGA[C/G]ACACAGAAACAGCAT	10025
rs550803713	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:891617	GGAACACCTGTGGCC[A/G]AGGCGGGGCTGAGTG	10025
rs550886496	snp	G/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:869031	TCCACAGGCGGGGGT[G/T]GAGGGAATGGCCGGC	10025
rs550978426	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:885516	AATGTGGGAGGTTGA[A/G]ATTCAGAGACAGGAA	10025
rs550992599	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:868591	GGCAGGTCTCCCTCT[A/G]CTCGCCGTCCCTCAC	10025
rs551052644	in-del	-/CC	0.0287284	0.116357	intron-variant	MED16	GRCh38.p7	19:889119	CTACTTCTTAACTGT[-/CC]CCCCAACCCTGGCCA	10025
rs551066198	snp	A/C	0.00318978	0.0398085	intron-variant	MED16	GRCh38.p7	19:888732	GTGGGGAGTGCACCC[A/C]GGAGGGCCCCCGTGG	10025
rs551092269	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:891242	AAAACAATGGAGGCC[C/T]GTGGTAGAGGGAACA	10025
rs551134357	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:891374	AGTAAGGTGGGAGCC[C/T]GGGAGGGCTGGGACC	10025
rs551163229	snp	A/G	0.0364509	0.129988	intron-variant	MED16	GRCh38.p7	19:871847	GGAGAGCGGGGAGAG[A/G]GGAGAGCGGGGAGCG	10025
rs551203996	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:874849	TGCTGCAACCTGGAT[A/G]ACACAGTGAGACCGT	10025
rs551257489	snp	A/G	0.00199481	0.0315187	intron-variant	MED16	GRCh38.p7	19:870729	TGGAGGGAAGGAGCC[A/G]TATGGATTCGGGGGG	10025
rs551335154	snp	C/T			intron-variant	MED16	GRCh38.p7	19:890309	CGATGACGATGACTC[C/T]AGGCAGGCTCCAGGT	10025
rs551408943	in-del	-/ATAA	0.00676609	0.0577691	upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:893381	ACACATTGGGCTAAT[-/ATAA]ATAGAGGTTAAATCT	10025
rs551455029	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:877314	TGTGGGCCTGTGTGC[A/G]CGCATGTGTCTGTAG	10025
rs551492284	snp	C/T	3.41338e-05	0.00413107	missense, intron-variant	MED16	GRCh38.p7	19:877017	TACTCCTCGTGCAGC[C/T]TCTCCACCAGGCTCT	10025
rs551510066	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:889973	GCCCTGAGACACCCT[A/G]AACAAGAATGATTCG	10025
rs551516997	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	MED16	GRCh38.p7	19:894242	AGTTTCACCATGTTG[A/G]CCAGGATGGTCTCAG	10025
rs551527022	snp	C/T			intron-variant	MED16	GRCh38.p7	19:880772	CTAAAATACAAAAAA[C/T]TAGCCGGGCGTGGCA	10025
rs551579725	snp	C/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:873775	CCACTGCCTGCCCCC[C/G]CCCGGGGGCCGCTGT	10025
rs551612699	snp	C/T			intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:891916	CACCTGTGGCCGAGG[C/T]GGGGCTGAGTGTGAT	10025
rs551732990	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:880553	GGTCTGCCATTGTAC[A/G]AGGGCCGGGGGGAGG	10025
rs551760587	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:874004	CAACAGATGCCTCTC[A/G]GATGGTGACTAGGGT	10025
rs551815676	snp	G/T			intron-variant	MED16	GRCh38.p7	19:878261	AGCCCCAGCCCCACG[G/T]GCCCCAGCAGCTCGC	10025
rs551832260	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:883996	CTTTACTGCCTCTGC[A/G]GCCACAATGGGCAGT	10025
rs551856225	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:872473	TACTGGGAGCTGAGA[A/G]GACCAGGGAAGGGAG	10025
rs551886059	snp	C/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:879592	ATGCCCAGCAGCTCA[C/G]CTTCCCGTGGTTGTC	10025
rs551946154	snp	A/G			intron-variant	MED16	GRCh38.p7	19:886426	TTGCTTTAGAGGACA[A/G]TGGGGAGGATTAAAC	10025
rs552014152	snp	G/T	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:884341	GTGGGGATGACGGGC[G/T]TGGCTCCGTGGGTGC	10025
rs552096630	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:887145	TGCGAGGAAGAGAAG[C/T]GTATCATACGTATCG	10025
rs552157806	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:872181	GCGATGGGATGAAGT[A/G]TCTTGGGGTCGGTGG	10025
rs552236536	snp	C/T	0.00199481	0.0315187	intron-variant	MED16	GRCh38.p7	19:888666	CTGTGAACTCCATCC[C/T]GACAAAACTGTTACC	10025
rs552337518	snp	A/G	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:889484	GAGGCCACTGAACAC[A/G]CAGGTGCTAATGACA	10025
rs552351101	snp	A/T	0.00199481	0.0315187	intron-variant	MED16	GRCh38.p7	19:883352	GCGGGGACCGAAGCC[A/T]GGCACGGTGGGCACG	10025
rs552425248	snp	C/G	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:893153	AGCGCCTCGGGTCTG[C/G]CGCCGCCATCTTCCT	10025
rs552427159	snp	C/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:889190	ATCTTAACTGTCCCC[C/G]CCAACCCTGGCCACG	10025
rs552462335	snp	A/C	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:892775	GCCCCCGAAGTCCCA[A/C]CAAGCGCCTTCAGCC	10025
rs552565472	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:883620	CTCGGGCGGGTAACA[A/G]CTGGGCCAGCAGGTG	10025
rs552623587	snp	C/G	0.00874735	0.0655527	intron-variant	MED16	GRCh38.p7	19:880209	CGCCCGCCGGGGGAG[C/G]GGCCTCCTGCTCTGC	10025
rs552724286	snp	A/G	0.000305364	0.0123527	intron-variant	MED16	GRCh38.p7	19:885764	TGATGGCCTGCGCCC[A/G]TTCACCTGCTCCGAC	10025
rs552751854	snp	A/G	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:876878	GACCACCTGCCACGG[A/G]GCCCCCACCTGCCAC	10025
rs552836083	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:870485	AGAATCATTTGAACC[C/T]GAGAGGCAGACGTTG	10025
rs552863610	snp	A/G			intron-variant	MED16	GRCh38.p7	19:886684	GCTGTGTAAGCACCA[A/G]CGGCTGCTGCGGGCA	10025
rs552899159	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:870221	AGACTAAGGGCAGAG[A/G]CTAAGGCAGGGCGCC	10025
rs553063090	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:881375	CAGATCCCGAAAGAT[A/G]AGATCTGCCTCCTAA	10025
rs553078648	snp	G/T	3.9633e-05	0.0044514	intron-variant	MED16	GRCh38.p7	19:885022	ACCTGCGGGGGAGGT[G/T]GGGGTGAGGGCTGAC	10025
rs553108663	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:869068	CCATCTGCCAGGTGG[A/G]CCCAGATGTCTGTGA	10025
rs553150965	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:884420	GCTGCTGGAGAGGTG[A/G]GGTGGGGTGGGGGGC	10025
rs553157746	snp	A/G	0.000186686	0.0096596	intron-variant	MED16	GRCh38.p7	19:871618	TGCCTGGAAGTGGCT[A/G]CCATCCCAAAAGCAC	10025
rs553168319	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:868951	GGCCTGGGGCCCTGG[C/T]GGGAGAGGGGAGAAC	10025
rs553189763	snp	A/G	0.00318978	0.0398085	intron-variant	MED16	GRCh38.p7	19:884146	GGTCCATTAGCGCTA[A/G]TCGGCAAATGCCTGT	10025
rs553245749	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:871408	GTTCTCTCACCAGGT[C/T]GGGGCCCCGGCTCTG	10025
rs553300043	snp	C/G	0.00279162	0.0372561	intron-variant	MED16	GRCh38.p7	19:868622	GCCTGCTCCCCACGT[C/G]CCCACCTGCCACAGG	10025
rs553335868	snp	G/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:883068	CACACCCCCAGCTAG[G/T]GGCCAGGGTACCCTC	10025
rs553383696	snp	G/T	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:874131	CCTAAATTTTTTTTT[G/T]GAGACAGAGTCTCAC	10025
rs553423636	snp	A/G	1.66527e-05	0.00288549	synonymous-codon	MED16	GRCh38.p7	19:885866	GCGCATGAACAGGGA[A/G]GGCAGGATCTCCGTG	10025
rs553443536	snp	A/T	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:887669	AGACTCTGTCTCAAA[A/T]AAAATGTATTTGGTT	10025
rs553443853	in-del	-/C			intron-variant	MED16	GRCh38.p7	19:876897	CCACCTGCCACGGGG[-/C]CCCCACCTGCCACGG	10025
rs553444828	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:888479	CTGTGAGCCAAGATC[A/G]CATCACTGCACTCCA	10025
rs553456946	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:890514	CTCCACAGCAGATAA[C/T]AGGTGGCTTTTTTGC	10025
rs553509559	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:870315	CCTGTAATCCCAGCA[C/T]TTTGGGAGGGCGAGG	10025
rs553582024	snp	C/G	1.82964e-05	0.00302455	utr-variant-3-prime	MED16	GRCh38.p7	19:868091	CAAGGTCCGCCTGGA[C/G]CCCCGGCCGTCACGG	10025
rs553596640	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:889277	TTACTAAATCAGAGG[A/G]TGGGCTGCATTCAGA	10025
rs553602064	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:890742	TTCGATCCCGCACAC[A/G]GGGCGATCTCATGTC	10025
rs553642822	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:872303	ACGCTGCTCAGAGCC[C/T]TGCAGGGCCCAGGAC	10025
rs553706578	snp	A/G	5.45628e-05	0.00522288	intron-variant	MED16	GRCh38.p7	19:886209	GCGCCCGACTGTGGA[A/G]AAGGGAGGGAGGGAG	10025
rs553749129	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, downstream-variant-500B	MED16, RNU6-9	GRCh38.p7	19:893691	CAACCTCCGCCTCCC[A/G]GGTTGAAGCGATTCT	10025
rs553768614	in-del	-/GAGCCCCGAGCCCC	0.00478085	0.0486577	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:892872	TCCGCCGCAAACCCT[-/GAGCCCCGAGCCCC]GAGCCCCGAGCCCCG	10025
rs553785908	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	MED16, RNU6-9	GRCh38.p7	19:893495	ATTCGTGCTCGCTTC[C/G]GCAGCACATATACTA	10025
rs553810016	snp	C/T	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:875029	ATCAGCCGGGCGTGG[C/T]GGCACGTGCCTGTAA	10025
rs553961971	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:880603	CTCATGGAAAAGAGA[A/G]TATGAAAGGAGTCCC	10025
rs553969652	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:892079	GCGGGGGCTGAGTGT[C/G]ACAGGGAACAGAGGG	10025
rs553998103	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:880398	CCGCCCCTCCCAGCT[A/G]GGCCCATGTCCTGGC	10025
rs554089365	snp	C/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:875944	TAGGACACCCCATCT[C/G]TACAAAAAATAGAAA	10025
rs554123086	snp	G/T			intron-variant	MED16	GRCh38.p7	19:868658	TGCCCATGCTTCTCC[G/T]CCCCCCAGCAATGCT	10025
rs554212344	snp	A/G	0.000139504	0.0083506	intron-variant	MED16	GRCh38.p7	19:881753	CAGGAAGGCAATGGA[A/G]TAAAGACAGGCTGAG	10025
rs554213676	snp	C/T	0.00597247	0.0543191	intron-variant	MED16	GRCh38.p7	19:870785	GGAGCCGTGTGGATT[C/T]GGGGGGACCCGGGGC	10025
rs554233565	snp	C/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:873349	ACTCCAACTAGGGGC[C/G]GGGCTGAGGTGGTTT	10025
rs554338182	snp	G/T	0.00358779	0.0422022	intron-variant	MED16	GRCh38.p7	19:873062	TCCGAGGTGGGGCAG[G/T]GCTCCGAGGTGGGGG	10025
rs554395013	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:883026	ACTCAACGCCCCAGC[A/G]CCGGGGGAGGCAGCT	10025
rs554480555	snp	A/T	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:884757	CACACCCGAGATCCT[A/T]GCACTACTGGAGATC	10025
rs554486066	snp	A/C	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:881978	GGCACCATCTCACCC[A/C]CGATGGGGCAGACAG	10025
rs554509525	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:869340	ACTTCCACACCACCT[C/T]TGCCCAGACACCCGG	10025
rs554608065	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:871759	GTGTTTTGGTAGGGA[A/G]AGGGGAGCGGGGAGA	10025
rs554683886	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:879831	CCAGGGCCAGCCCCA[C/T]GTGCCCCAGCAGCTC	10025
rs554694527	snp	A/C	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:874425	ACCCTAATTTTTAAA[A/C]GAAACAGCCTGCCAG	10025
rs554767092	snp	A/G	0.00159617	0.0282053	intron-variant	MED16	GRCh38.p7	19:877400	ACCTCCCTGAGCCCC[A/G]ACTGCACTGGATGCC	10025
rs554831907	in-del	-/G	0.00159617	0.0282053	intron-variant	MED16	GRCh38.p7	19:887842	AGACAACTGGGTCTC[-/G]GGGGCTGGGGTGGGG	10025
rs554900562	in-del	-/C	0.000815505	0.0201764	intron-variant	MED16	GRCh38.p7	19:879908	GTCAATGCCCACCAG[-/C]CCCGGCCCCACGTGC	10025
rs554929242	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:888440	GAGGCAGGAGAATCG[C/T]TTGAACCCAGGAGGC	10025
rs555001177	snp	G/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:878639	AACCCCAGCCCCACG[G/T]GCCCCAGCAGCTCAC	10025
rs555082373	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:876489	CAGACTGGGAACACT[A/G]GAGAGGGGAGCCGTC	10025
rs555120985	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:880718	TGAGCTCAGGGGTTC[A/G]AGACCAGCCTGGGCA	10025
rs555140594	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:885534	TCAGAGACAGGAAGA[A/G]GCTGCGCTGTGGCCA	10025
rs555142575	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:882560	TGGCCCAGAGAGCAC[A/G]TGTGGGGGGTCCTGC	10025
rs555317427	snp	G/T	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:887583	AGGCAGGAGAATCAC[G/T]TGAACCTGGGAGGTG	10025
rs555317694	snp	C/T	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:884590	CCACAGCCGCCCACA[C/T]GCCTGCAGCCCCTCA	10025
rs555372238	snp	A/G	0.000170019	0.00921849	intron-variant	MED16	GRCh38.p7	19:868278	GCTGAGGTTAACCGC[A/G]CCGAGGAGAGTCCAG	10025
rs555376287	snp	C/T	1.77219e-05	0.00297668	missense, intron-variant	MED16	GRCh38.p7	19:889742	TCTCCCAGCTATTAG[C/T]CAGGTGGTCCGCCAT	10025
rs555405198	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:887342	GAGACTATGTTAAAG[A/G]AGCACATGTGCCTTT	10025
rs555504067	snp	C/G	0.000497512	0.0157642	intron-variant	MED16	GRCh38.p7	19:871291	TCTCAGCACCCCTGA[C/G]TGGGGCACCGCCCGG	10025
rs555514961	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:869043	GGTGGAGGGAATGGC[C/T]GGCCTCACACCATCT	10025
rs555543361	snp	A/G	0.000270893	0.011635	missense	MED16	GRCh38.p7	19:871113	ACTGCAGACGAAGGG[A/G]CTGCTTGGGCTGCAG	10025
rs555543977	snp	A/G	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:890725	CCAACGCTCCAGCCC[A/G]ATTCGATCCCGCACA	10025
rs555544825	snp	C/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:883840	TCACCACGAGGCCCA[C/G]GGGAAGGAATGAGGC	10025
rs555573122	snp	A/C/G	0.000118478	0.00769595	missense	MED16	GRCh38.p7	19:868455	TCCCACTGCTTCACC[A/C/G]CCGTGGTTCTGTTGG	10025
rs555581622	snp	C/T	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:886617	AACCCAGGCGGGGGC[C/T]GTCAGGCCCTGGGCC	10025
rs555610707	snp	A/G			intron-variant	MED16	GRCh38.p7	19:877494	ACAGCTCCTAGTTAC[A/G]AAGCTCCTAATACGT	10025
rs555611626	snp	C/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:870744	GTATGGATTCGGGGG[C/G]GTCCTGGGGCAGGAC	10025
rs555631208	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:873614	GTCGGGTCAGCTCGG[A/G]CCTCTTGTACACACA	10025
rs555638133	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, nc-transcript-variant	MED16, RNU6-9	GRCh38.p7	19:893487	AACTCAATATTCGTG[C/T]TCGCTTCGGCAGCAC	10025
rs555719644	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:885588	AACCGAGGGATTGGG[C/T]GCCTCCAGATGCTGG	10025
rs555721534	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:889257	TAGAGAGGGGCTCTG[A/G]GATGTTACTAAATCA	10025
rs555807676	snp	A/C	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:888788	CGGCAATGCGCCGAC[A/C]ATGGCAGTCCCTGGG	10025
rs555833568	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:890541	TTGCACCCCGATTTG[A/G]TTCCAATTTTCTGTG	10025
rs555964654	snp	A/G	0.00159617	0.0282053	intron-variant	MED16	GRCh38.p7	19:874992	ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA	10025
rs556012822	in-del	-/CC	0.0144955	0.0838905	intron-variant	MED16	GRCh38.p7	19:889053	CTACTCTTAACTGTC[-/CC]CCCCAACCCTGGCCA	10025
rs556050849	snp	C/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:876833	CCACGGGGCCCCTGC[C/G]TGCCACAGGGACAGC	10025
rs556066386	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:878575	CCAGCCCCAGCCCCA[C/T]ATGCCCCAGCAGCTC	10025
rs556075367	snp	A/C/G	3.67838e-05	0.00428845	utr-variant-3-prime	MED16	GRCh38.p7	19:868079	GCCGGGTCACCACAA[A/C/G]GTCCGCCTGGACCCC	10025
rs556098129	snp	A/G			intron-variant	MED16	GRCh38.p7	19:880513	GCATCTTAGGGTGGT[A/G]GGCTGGGGCTGTCAC	10025
rs556138490	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:870238	TAAGGCAGGGCGCCC[C/T]GTACAGCGAGGCCAA	10025
rs556246007	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:870598	AGGGAGAGGGTGAAT[A/G]GAAGGGCTGGGTGCC	10025
rs556274464	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:893355	CAGTCAATAACTACG[C/T]TAGTTGCATTACACA	10025
rs556315009	snp	G/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:891477	ACGCAGCGGAGGGTC[G/T]GCGCTGGCCCAGGTG	10025
rs556406436	snp	C/G			intron-variant	MED16	GRCh38.p7	19:881724	CGCCAACTGAAAAAT[C/G]AGGGGCAGGAAAACA	10025
rs556561325	snp	C/G			upstream-variant-2KB, nc-transcript-variant	MED16, RNU6-9	GRCh38.p7	19:893560	CCTGCGCAAGGATGA[C/G]ACGCAAATTCGTGAA	10025
rs556597871	snp	G/T	0.00358779	0.0422022	intron-variant	MED16	GRCh38.p7	19:873036	GGCAGGGCTCCGAGG[G/T]GGGGCAGGGCTCCGA	10025
rs556600165	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:881844	CATGCCGCCCTGCTC[C/T]CATGCCCAGAAGACC	10025
rs556644258	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:880240	AGGGTGTGGAGAGCC[A/G]GGGCTGCCCATCCAG	10025
rs556683329	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:872727	GTGGAGGTGTGGATG[A/G]AGACTTGATTTCAAG	10025
rs556733843	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:883438	CACGTGGGGCGGTGC[A/G]TGAAGAGCTGGGCAT	10025
rs556777148	snp	A/G	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:880926	TGAGACTCCAACTCA[A/G]AAAAAAAAAGAAAAA	10025
rs556782345	snp	C/T			intron-variant	MED16	GRCh38.p7	19:886749	ATTGACATACGGAAA[C/T]ATCCACCCTTCTTTC	10025
rs556826884	snp	A/G	3.34739e-05	0.00409095	missense	MED16	GRCh38.p7	19:881682	TGGCCGATAGGATCC[A/G]CCATTTGAGAATTGT	10025
rs556854488	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:882848	CGGACGGGCCATCAC[A/G]GTCACAGAGCCTTGA	10025
rs556950283	snp	A/C	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:877715	TCAATGCCCACCAGC[A/C]CCTGCCCCACGTGCC	10025
rs557020250	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:874152	AGAGTCTCACTCTGT[C/T]GCCCAGGCTGGAGTG	10025
rs557055590	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:873907	GCCCCCTGCTCCGAG[A/G]TGAACTCTGTGAACA	10025
rs557103090	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:881391	AGATCTGCCTCCTAA[C/T]TGGGAACCCATCAGA	10025
rs557129161	snp	A/G	0.0023933	0.0345097	intron-variant	MED16	GRCh38.p7	19:885321	GAATCCAGGCGACCT[A/G]GTGTGGTCGGCTCAA	10025
rs557140832	snp	A/C/G	0.00070895	0.0188154	intron-variant	MED16	GRCh38.p7	19:877211	CCCAAGGAGAGCCCG[A/C/G]TGAGATGGGGCTGCG	10025
rs557192740	snp	A/G	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:884515	AGGATTCCGTGCACC[A/G]CCCCTGCCCGGTCTG	10025
rs557286432	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:869276	TGAGGTGCAGGGAAG[A/G]TGCTTGTGACGCTCC	10025
rs557316056	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:880420	TGTCCTGGCTGACAC[A/G]CCCCTCAAGGAGCGC	10025
rs557359337	in-del	-/C/T/TT	0.00358779	0.0422022	upstream-variant-2KB, nc-transcript-variant	MED16, RNU6-9	GRCh38.p7	19:893516	CATATACTAAAATTG[-/C/T/TT]GAACGATACAGAGAA	10025
rs557420422	snp	A/G			intron-variant	MED16	GRCh38.p7	19:874634	GCGTCTCAGCCCCCA[A/G]GAGTAGAGAGAGGTG	10025
rs557539588	snp	A/G	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:883524	GGGAGAGATGGGTGC[A/G]GTGGGGACTGTCCCA	10025
rs557568677	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:888000	CTGAGGTTAGGAGTT[C/T]GAGACCACCCTGACC	10025
rs557610171	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:870393	TTGCAAAACCGCCTC[C/T]ATACCAAAAATACAA	10025
rs557691385	snp	C/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:890855	GGCCAGGGTGAGTGA[C/G]AGGTGGCCTGAGAGA	10025
rs557710345	snp	C/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:887063	TGGCCTGGGCAACGA[C/G]AGCAAAACTTTGTCT	10025
rs557733758	snp	A/G			intron-variant	MED16	GRCh38.p7	19:873966	AGCCACCCCCGGCTG[A/G]CAGCTGGCGGCGGTT	10025
rs557801498	snp	A/G	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:872632	AGAAATCACAGCTGG[A/G]GCAGGACAGAGTGTA	10025
rs557803150	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:886534	CAGGTGGTCCCTGTT[A/G]CAACGACTTGGCTCT	10025
rs557854422	snp	G/T			upstream-variant-2KB, downstream-variant-500B	MED16, RNU6-9	GRCh38.p7	19:893637	GAATCTTGCTCTGTT[G/T]CCCAGGCTGGAATGC	10025
rs557948773	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:870559	GAGTGAGACCCTGTC[A/G]GGGAGACAAAAAAAA	10025
rs557953962	snp	C/T	0.00318978	0.0398085	intron-variant	MED16	GRCh38.p7	19:876738	AACCCCCACATCTGC[C/T]GTGGGGACCTCTACA	10025
rs558004992	snp	A/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:870829	AGGGAGCCGTGTGGA[A/T]TCGGGGGGTCCCGGG	10025
rs558016879	snp	G/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:889354	CTCCAGTGAAAGAGA[G/T]AACTCACTAAGAACG	10025
rs558061095	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, nc-transcript-variant	MED16, RNU6-9	GRCh38.p7	19:893527	AATTGGAACGATACA[A/G]AGAAGATTAGCATGG	10025
rs558078977	snp	A/C	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:880670	CACGCCTGTAATCCT[A/C]GCACTTTGGGAGGCT	10025
rs558089844	snp	G/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:873371	AGGTGGTTTTGAGGG[G/T]CAGGGGCAGGGAAGC	10025
rs558102960	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:893005	GCAGGCCCCGCCACG[A/G]CTGCGCCGCGTTCCC	10025
rs558125858	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:892002	GAGGCGGGGCTGAGT[A/G]TGACGGGGAACACCT	10025
rs558198820	snp	A/T	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:868653	GCCTCTGCCCATGCT[A/T]CTCCTCCCCCCAGCA	10025
rs558257253	snp	C/T			intron-variant	MED16	GRCh38.p7	19:883607	GTGAGACGTGGCTCT[C/T]GGGCGGGTAACAGCT	10025
rs558267730	snp	G/T	0.000333795	0.0129146	intron-variant	MED16	GRCh38.p7	19:873596	GTCTACAAGGAGACG[G/T]GGGTCGGGTCAGCTC	10025
rs558363657	snp	G/T	1.85286e-05	0.00304368	missense	MED16	GRCh38.p7	19:871954	CTTGGTGAGCAGGCG[G/T]AAGAGCAGGGACATG	10025
rs558387974	snp	C/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:877615	CTGTGGTCCCTTCCC[C/G]CGGGGGCGCCTCCCT	10025
rs558439988	snp	G/T			intron-variant	MED16	GRCh38.p7	19:876235	GCAGCTGCCGGCTGA[G/T]CTCGTTAGATCTGAG	10025
rs558468070	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:882043	GCAAACCCTAACACT[C/T]GCTCGGCCTTAGCCA	10025
rs558471017	in-del	-/GCCCCA			intron-variant	MED16	GRCh38.p7	19:877793	CCAGCCCCAGCCCCA[-/GCCCCA]CGTGCCCCAGCAGCT	10025
rs558518905	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:888535	TCTCCAAAAAAAAAA[A/G]AAAAAAAAGATAAAG	10025
rs558547532	in-del	-/G	6.18671e-05	0.00556145	intron-variant	MED16	GRCh38.p7	19:872153	TGTGGCTGGGGCGGC[-/G]GGGGGGCAGATGGCG	10025
rs558603741	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:869710	GCCGGGGCCTTCCCC[A/G]GAGCAGGGCTGCTGG	10025
rs558613868	snp	A/C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:868755	TCCCTCTGGGACGTG[A/C/T]TCCCTCCACCACCCT	10025
rs558695313	in-del	-/C	0.00438332	0.0466095	intron-variant	MED16	GRCh38.p7	19:889017	GCCTGAACCCAGGTG[-/C]CCCCCCAACCCTGGC	10025
rs558733973	in-del	-/ACAGAA	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:882708	GCAGCTGAGGCAGCC[-/ACAGAA]ACAGAAACAGAAACA	10025
rs558738987	snp	A/G	0.00716266	0.059414	intron-variant	MED16	GRCh38.p7	19:874470	GCCTGTAATCCCAGC[A/G]CTTTGGGAGGCAGAG	10025
rs558757793	snp	C/G			intron-variant	MED16	GRCh38.p7	19:886978	CAGCTACTCAGGAGG[C/G]TGAGGCAGGAGAATT	10025
rs558803866	snp	C/T	0.000150014	0.00865935	synonymous-codon	MED16	GRCh38.p7	19:875329	GTGGGGGCGCAGCAG[C/T]GACTTCAGGGTGGAG	10025
rs558944401	snp	C/T	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:870922	GGAGCCGTGTGGATT[C/T]GGGGGGACCTGGGGC	10025
rs558970662	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:875130	GATCGCACCACTGCA[C/T]TCCAGCCTGGGCAAC	10025
rs559012987	snp	A/G	0.000399281	0.0141238	missense	MED16	GRCh38.p7	19:875420	GACAGCTTGCAGAGC[A/G]AGGCCTTCATGGCCA	10025
rs559105777	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:873659	CACCCCTCGGTCCTT[C/T]GACCTGCACTGAGTG	10025
rs559142767	snp	C/T	5.89084e-05	0.00542685	intron-variant	MED16	GRCh38.p7	19:879891	CTCGCCTTCCCCTGG[C/T]TGTCAATGCCCACCA	10025
rs559182344	snp	C/T	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:882832	CATGAGGTCTCTGCC[C/T]CGGACGGGCCATCAC	10025
rs559211209	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:885428	GGTGGGATTCGGTTC[A/G]GGACACTGAGACGGG	10025
rs559279225	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:882847	CCGGACGGGCCATCA[C/T]GGTCACAGAGCCTTG	10025
rs559286333	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	MED16	GRCh38.p7	19:867905	GAGGACACAGGCTCC[C/T]GGCACCAAATCGAGG	10025
rs559303967	snp	C/T	0.00597247	0.0543191	intron-variant	MED16	GRCh38.p7	19:877305	ACGCCCGTGTGTGGG[C/T]CTGTGTGCGCGCATG	10025
rs559317110	snp	A/G	0.00120933	0.0245602	intron-variant	MED16	GRCh38.p7	19:868257	TTCAACAGCCCTGCA[A/G]GGCGGGCTGAGGTTA	10025
rs559396148	snp	A/G	0.00159617	0.0282053	intron-variant	MED16	GRCh38.p7	19:881479	GGTGTGAGCTCCCAC[A/G]ACCCCGTGGCCTGTG	10025
rs559436266	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, nc-transcript-variant	MED16, RNU6-9	GRCh38.p7	19:893558	CCCCTGCGCAAGGAT[A/G]ACACGCAAATTCGTG	10025
rs559534497	snp	C/T	0.00279162	0.0372561	intron-variant	MED16	GRCh38.p7	19:883736	GCCCAGCGGGGGCAC[C/T]GGGCAGTGAAGGTGC	10025
rs559570794	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:880779	ACAAAAAATTAGCCG[A/G]GCGTGGCAGCACGCG	10025
rs559620160	snp	A/G	0.000111182	0.00745509	synonymous-codon	MED16	GRCh38.p7	19:879952	CTTCCCGTGGCTGTC[A/G]ATCCCCACCAGGGCC	10025
rs559652645	snp	C/T	0.000965584	0.0219513	synonymous-codon	MED16	GRCh38.p7	19:871138	CTGCAGGCGGCTAAC[C/T]AGGCCGTCGCTGGCT	10025
rs559660453	snp	C/T	0.00199481	0.0315187	intron-variant	MED16	GRCh38.p7	19:883875	CAAGGCCCTGGGGAC[C/T]GGGCGAAGGAACGAG	10025
rs559685719	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:887390	AACAAAAATTTGGCC[A/G]GACGCGGTGGCTCAC	10025
rs559786814	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:882882	CCTGCAAACCCGTAT[A/G]GGGGTCCTGTGAGCA	10025
rs559823035	snp	A/G	0.00159617	0.0282053	intron-variant	MED16	GRCh38.p7	19:882669	CCTCGGCTGCTAACC[A/G]CAGACACGTGGGAAC	10025
rs560091649	snp	A/G	0.00517822	0.0506191	intron-variant	MED16	GRCh38.p7	19:873710	AAGGGGACCCACACC[A/G]GGAACGAGAAGGGGG	10025
rs560108615	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	MED16	GRCh38.p7	19:867731	CAGGCAGACAACACA[C/T]TGAAAGGCAGATGCC	10025
rs560109850	snp	A/G	0.00030326	0.0123101	intron-variant	MED16	GRCh38.p7	19:890364	GAAGGTCACAGAACT[A/G]CTGTCAGCCGAGTCG	10025
rs560126832	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:888633	GGCTGCACACTCTCA[A/G]TGGGTGAGTTCTAAG	10025
rs560148766	snp	A/G			intron-variant	MED16	GRCh38.p7	19:884502	AACCAGGTTCCGGAG[A/G]ATTCCGTGCACCGCC	10025
rs560168876	snp	C/T			upstream-variant-2KB	MED16	GRCh38.p7	19:894471	CCACCGCGGCCTCAC[C/T]GCATGATTTTTGCAA	10025
rs560194799	in-del	-/C	0.268576	0.249309	intron-variant	MED16	GRCh38.p7	19:889054	ACTCTTAACTGTCCC[-/C]CCCCAACCCTGGCCA	10025
rs560210652	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:891510	TGATGATGGGGGCAG[C/G]AAGTGGACACTAGCT	10025
rs560235780	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:893404	AGGTTAAATCTCTAG[A/G]TCATTTAAGAGAAGT	10025
rs560253253	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	MED16	GRCh38.p7	19:867968	GACGCGGGCCTGGGC[A/G]CAGAGGGCGTTTATT	10025
rs560272527	snp	C/T	0.000798403	0.0199641	utr-variant-5-prime, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:893125	AGCGGGCGTCCGCGG[C/T]GCGATCTTCCCTAGC	10025
rs560403318	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:889460	GAACAGCCACCCTCA[A/G]TTAAATGAGAGGCCA	10025
rs560453924	snp	A/G			upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:893447	ACAGACATTTGTTCC[A/G]GGGGCTTTAAATAGC	10025
rs560554377	snp	A/G	3.39368e-05	0.00411913	intron-variant	MED16	GRCh38.p7	19:868293	GCCGAGGAGAGTCCA[A/G]GGCGAGCGGTGGCTC	10025
rs560612786	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:870468	GGGAAGGCTGAGGTA[A/G]GAGAATCATTTGAAC	10025
rs560666572	snp	A/C	1.67713e-05	0.00289575	synonymous-codon	MED16	GRCh38.p7	19:875275	GGTGCAGATCTCGGT[A/C]AGCCGGTCGCCGGGG	10025
rs560686713	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:872776	AGGGAGCTGGGGAGG[A/G]TAAGGGGTGGGGGCA	10025
rs560711847	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	MED16	GRCh38.p7	19:894699	GTACTTTGGGAGGCC[A/G]AGGTCTGAGGACAGC	10025
rs560719871	snp	C/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:887762	CAGTAAGAGATGCCA[C/G]ACACAGAAGGCTACG	10025
rs560725353	snp	G/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:872409	CCACCTGCACGTGGA[G/T]GAGCAGCCGCCCCCT	10025
rs560757709	snp	C/T	0	0	intron-variant	MED16	GRCh38.p7	19:890902	CAGTGGGCCGGGCAC[C/T]TGGGGAACAGGGCGG	10025
rs560860715	snp	A/G			intron-variant	MED16	GRCh38.p7	19:880444	GGAGCGCAGGGGAGG[A/G]GGGCACTACAGGTGG	10025
rs560865015	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:884696	GCGTGGAAGGATGGA[A/G]GAGTCTATACGCCTA	10025
rs560887615	snp	A/C/G	1.92439e-05	0.00310187	missense, synonymous-codon	MED16	GRCh38.p7	19:880095	CGGCCATGGTCTGCA[A/C/G]TGAGAGCCGGTGCAC	10025
rs560956808	snp	A/G/T	0.00336465	0.0408785	intron-variant	MED16	GRCh38.p7	19:871668	GTGCTAGGAACTGGG[A/G/T]AAATAGCAGATATCA	10025
rs560965891	snp	A/G	0.00279162	0.0372561	intron-variant	MED16	GRCh38.p7	19:871814	GGGAGAGCGGGGAGA[A/G]GGGAGAGCGGGGAGA	10025
rs560972852	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	MED16	GRCh38.p7	19:894167	CAGCCTCCCGAGTAG[C/T]TGGGACTACAGGCGC	10025
rs560993850	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:871459	CAGAGTTCTCTCCCC[A/G]TCTCTGGCCTGTCAT	10025
rs561020858	snp	C/G	0.000107997	0.00734758	intron-variant	MED16	GRCh38.p7	19:868975	GGAGAACGTGAGGGA[C/G]GCCTGGGCACCACGA	10025
rs561063579	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:890667	CCAGTGACACACACC[A/G]TCTAGAAAACTGGGG	10025
rs561070838	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:881415	CATCAGAACCCAGAA[A/G]GCTGAGCTCCTACAG	10025
rs561082433	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:873960	AGCTGCAGCCACCCC[C/T]GGCTGGCAGCTGGCG	10025
rs561121931	snp	C/T			intron-variant	MED16	GRCh38.p7	19:878016	CCGTGGTTGTCAACG[C/T]CCACCAGCCCCAGCC	10025
rs561267539	snp	A/C	0.00557542	0.0525036	intron-variant	MED16	GRCh38.p7	19:877845	TCAATGCCCACCAAG[A/C]CCAGCCCCACATGCC	10025
rs561276369	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:876959	CACGGGGCCCCACCT[A/G]CCACGGGCCCCCACC	10025
rs561363569	snp	C/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:873152	TCCGAGGTGGGGCAG[C/G]GCTAGGAAGTGGGGC	10025
rs561414792	snp	C/T			intron-variant	MED16	GRCh38.p7	19:891468	AGCCGGGAGACGCAG[C/T]GGAGGGTCTGCGCTG	10025
rs561445489	snp	A/C	0.00557542	0.0525036	intron-variant	MED16	GRCh38.p7	19:882146	TCCGCTGCCTGACAG[A/C]CCCTGCGTGAAGACG	10025
rs561488101	snp	C/T	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:875670	CTGGGAGCGGCTCTG[C/T]CTCTGGTGGGGGCCC	10025
rs561515488	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:877468	CTACCCCGTGAAAGG[C/T]GGTCCTCTCAACAGC	10025
rs561530252	snp	C/T	0.00159617	0.0282053	intron-variant	MED16	GRCh38.p7	19:885068	TGGCCACGCCACCAC[C/T]GGAGCCTGAGCTGCG	10025
rs561691924	snp	A/G			intron-variant	MED16	GRCh38.p7	19:882067	TTAGCCAGCTCAGCC[A/G]GGATTCCCATCCCTC	10025
rs561713754	snp	A/C/T	2.23796e-05	0.00334504	synonymous-codon	MED16	GRCh38.p7	19:880147	GAAGGCCAGGGCCAG[A/C/T]CCTGTGGGGCACAGG	10025
rs561849865	snp	G/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:883932	CTCTTCACCTGCCTG[G/T]TGACTCACTACAAGC	10025
rs561864087	snp	G/T	0.00279162	0.0372561	intron-variant	MED16	GRCh38.p7	19:880442	AAGGAGCGCAGGGGA[G/T]GGGGGCACTACAGGT	10025
rs561935704	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:886736	TTGTCAAGTCATTAT[C/T]GACATACGGAAACAT	10025
rs562068194	in-del	-/GCTCAGGGGCA	0.00438332	0.0466095	intron-variant	MED16	GRCh38.p7	19:868322	TCTTGCAGCAGCCGG[-/GCTCAGGGGCA]GCTGAGGGGTAGCTG	10025
rs562071762	snp	C/T	5.36745e-05	0.00518019	intron-variant	MED16	GRCh38.p7	19:873409	TGATGAGATGGGGGC[C/T]CAGGTGGGGGGCGGG	10025
rs562092869	snp	A/C	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:881289	AGTTCCACCAAGTTC[A/C]CCAGGCTCCCTTGTT	10025
rs562228701	snp	C/T	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:868342	GGGGCAGCTGAGGGG[C/T]AGCTGAGGAGTAGCT	10025
rs562247378	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:888604	GAGTGTATACGAAAC[C/T]TCTGGACCGTGTGGG	10025
rs562329796	snp	A/G	6.8937e-05	0.00587058	intron-variant	MED16	GRCh38.p7	19:868538	GGGTTCCCACTTCCA[A/G]GCGGGCCTCCCTTAC	10025
rs562468456	snp	A/C	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:874527	AGCCTGGGCAAGCTG[A/C]TTAGCCTTTCTGCCT	10025
rs562469124	in-del	-/GGTGG	0.00358779	0.0422022	intron-variant	MED16	GRCh38.p7	19:884415	AGAGGCTGCTGGAGA[-/GGTGG]GGTGGGGTGGGGTGG	10025
rs562565656	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:869418	CTGCCCTCGGTGGTG[A/G]GTGGGGGACCTGGGT	10025
rs562572169	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:882294	CAGAGGATGGCTTGA[A/G]TCCAGGAGTTCAAGA	10025
rs562620638	in-del	-/ACAAGGAGAGCACGCAGAG	0.00517822	0.0506191	downstream-variant-500B	MED16	GRCh38.p7	19:867685	CAGAGACACGCAGAA[-/ACAAGGAGAGCACGCAGAG]ACAGTATAGAGACAG	10025
rs562627953	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:871791	GGGAGAGGGGAGAGC[A/G]GGGAGAAGGGAGAGC	10025
rs562634336	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	MED16	GRCh38.p7	19:867520	CGGGACCCCTGGGGA[C/T]AGCAACAGAAACGGC	10025
rs562763547	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	MED16	GRCh38.p7	19:868030	GGTTCAGCGCTCTCC[A/G]CGGGTGAGGCAAGGA	10025
rs562787343	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:869158	CCCACACGGAGGAGG[A/G]TTGGTCTCCCAGGTG	10025
rs562827905	snp	A/C/G	0.000136139	0.0082494	intron-variant	MED16	GRCh38.p7	19:871704	GAGCCACTGCCACCT[A/C/G]CAGGGGCTTATGTTC	10025
rs562855094	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:892433	CCAGGCCCAACCCCT[A/G]AAACTCCCCAGTCCC	10025
rs562898107	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:889036	CCCAACCCTGGCCAC[A/G]CCTACTCTTAACTGT	10025
rs562928242	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:893066	CCGCCCTCGCCGGGC[C/T]CCCGCAGCCCCGCAC	10025
rs562998150	snp	C/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:872368	TCCACAAGACTAAGA[C/G]GAGGCTCTGGCTGAG	10025
rs563008501	snp	A/G	0.00398564	0.0444627	intron-variant	MED16	GRCh38.p7	19:869711	CCGGGGCCTTCCCCG[A/G]AGCAGGGCTGCTGGA	10025
rs563076638	snp	G/T	0.0023933	0.0345097	intron-variant	MED16	GRCh38.p7	19:879475	CCCCTGGTTGTCAAT[G/T]CCCACCAGCCCCAGC	10025
rs563090751	snp	C/G/T	3.43502e-05	0.00414417	intron-variant	MED16	GRCh38.p7	19:875236	CCCGGGCGTGGAAAA[C/G/T]GACCCACCGACGTCG	10025
rs563128075	snp	A/C	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:874870	GTGAGACCGTCTCTA[A/C]AAGCCTGGGTGTGGT	10025
rs563147182	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:879927	GGCCCCACGTGCCCC[A/G]GCAGCTCACCTTCCC	10025
rs563161716	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:871435	TCTGCCTGCCTGGCT[A/G]GGTGACCCCAGAGTT	10025
rs563166034	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	MED16	GRCh38.p7	19:894649	ATTTAACGTTCTTAG[C/T]GGCCCGGGTGTGGTG	10025
rs563172680	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:870201	CTGACATCCAGGGGG[A/G]CCAGAGACTAAGGGC	10025
rs563266348	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:887154	GAGAAGTGTATCATA[C/T]GTATCGTACGGCTCC	10025
rs563302682	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:890379	GCTGTCAGCCGAGTC[A/G]ACAGCTCAGGGAACA	10025
rs563331382	snp	A/G			intron-variant	MED16	GRCh38.p7	19:872515	GGCCCCTGGCAGCCT[A/G]AAGCCCCACAAAAAG	10025
rs563351108	snp	C/G	0.000137698	0.0082964	intron-variant	MED16	GRCh38.p7	19:873432	GGGGCGGGGCCTTAG[C/G]GGAGAGCATGGCGCA	10025
rs563354488	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:874314	AGACGGGGTTTCACC[A/G]TGTTAGCCAGGATGA	10025
rs563394035	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:877444	ACTCGTCTGCTTTAC[C/T]TGAGGAGTCTACCCC	10025
rs563409424	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:881173	GTAGGCACTGAAGAG[C/T]GTGCAGACTCACTCA	10025
rs563412854	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, downstream-variant-500B	MED16, RNU6-9	GRCh38.p7	19:893952	CGAAGTCACCGACCC[C/T]GTTGAGTATTCCTAC	10025
rs563422460	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:873716	ACCCACACCGGGAAC[A/G]AGAAGGGGGCGATGG	10025
rs563458694	snp	A/G	0.00478085	0.0486577	intron-variant	MED16	GRCh38.p7	19:876912	GCCCCACCTGCCACG[A/G]GGCCCCCACCTGCCA	10025
rs563614295	snp	C/T	0.00279162	0.0372561	intron-variant	MED16	GRCh38.p7	19:880795	GCGTGGCAGCACGCG[C/T]CTGTAGTCCCAGCTA	10025
rs563725902	snp	A/G	0.00597247	0.0543191	intron-variant	MED16	GRCh38.p7	19:875592	CGCCTCTGCACCTCA[A/G]CAACCTCATGGCAAA	10025
rs563849886	snp	A/G/T	0.000118574	0.00769904	synonymous-codon	MED16	GRCh38.p7	19:880003	CATAGCCTTTAAGTG[A/G/T]ACGGCGGGGCCCGCG	10025
rs563865135	snp	C/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:868961	CCTGGCGGGAGAGGG[C/G]AGAACGTGAGGGAGG	10025
rs563975440	snp	A/G	0.00279162	0.0372561	intron-variant	MED16	GRCh38.p7	19:884683	GCCGCCGCAGCGGGC[A/G]TGGAAGGATGGAGGA	10025
rs564080110	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:870159	TAAGGCGTCTCTCTC[C/T]ATCCACAGAGGGATC	10025
rs564159478	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:885687	GCCCGTGGAGGCCCG[C/T]GCGGGTCTCCACCCC	10025
rs564218872	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:883151	TCCTAAATGAGGGGG[A/G]ACTTGAGGCAGGGAG	10025
rs564246110	snp	C/T	0.000110846	0.00744385	intron-variant	MED16	GRCh38.p7	19:890086	AACACAGGGCCCCCC[C/T]GCTCCGGGATCCGGG	10025
rs564256059	snp	C/T	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:882649	CCAGTGGACAGGCCA[C/T]GCCACCTCGGCTGCT	10025
rs564260157	in-del	-/T	0.0402882	0.136092	intron-variant	MED16	GRCh38.p7	19:889109	CCTGGCCACGCCTAC[-/T]TCTTAACTGTCCCCA	10025
rs564294570	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:870471	AAGGCTGAGGTAGGA[A/G]AATCATTTGAACCCG	10025
rs564301785	snp	A/G	6.7113e-05	0.00579241	synonymous-codon	MED16	GRCh38.p7	19:885923	GCTCACGCACACCTT[A/G]TAGAACTGCACGGGC	10025
rs564333973	snp	C/T	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:889870	CACTGCGTTGCAGGA[C/T]GGCACAGCGCCTGGG	10025
rs564370235	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:893423	TTTAAGAGAAGTCGG[C/T]CTATGTGTACAGACA	10025
rs564391362	snp	C/T	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:883666	GACGAGGAGGAGTGT[C/T]GGAGCCCAGGACTGC	10025
rs564392816	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:888928	AGCTGGGGTGGCTGT[A/G]AGGCCTTTGCCACGA	10025
rs564485562	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:883903	GAGCCCTGGGAGAAG[A/G]AATGGCAGCAGCCCT	10025
rs564487407	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:876018	CAAGGAGGGAGAGGG[C/T]GAGGTCTCGCCATCA	10025
rs564563035	snp	G/T			intron-variant	MED16	GRCh38.p7	19:891301	GAGCCTGGGGCTGGG[G/T]CCGAGGGGGAACATG	10025
rs564598227	snp	C/T			intron-variant	MED16	GRCh38.p7	19:874766	TAATCCCAGCTACTC[C/T]AGAGGCTGAGGCGAG	10025
rs564707774	in-del	-/GCCCCA			intron-variant	MED16	GRCh38.p7	19:878253	CCAGCCCCAGCCCCA[-/GCCCCA]CGGGCCCCAGCAGCT	10025
rs564726752	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:870664	CCACTAGGGGATGGA[A/G]TTAGGGGCACCTAGA	10025
rs564738619	snp	A/G	0.000283596	0.0119045	synonymous-codon	MED16	GRCh38.p7	19:873538	GTGTGTTCATGTCCA[A/G]CACAAATTCCTCCGT	10025
rs564761362	snp	A/G	0.0178098	0.0926698	intron-variant	MED16	GRCh38.p7	19:873073	GCAGGGCTCCGAGGT[A/G]GGGGAGGGCTCCGAG	10025
rs564762282	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:888082	GGTGGCGGGCGCCTG[C/T]AATCCCAGCTATTCA	10025
rs564929111	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:884894	CTCCGCAGCCGGCGG[A/G]AGACTCACCCACGGG	10025
rs564945235	snp	C/T			intron-variant	MED16	GRCh38.p7	19:881044	AACAGCCCTGAGCCC[C/T]GAGCGGGTTTTGATA	10025
rs564952588	snp	C/T	0.0023933	0.0345097	intron-variant	MED16	GRCh38.p7	19:869367	CCGGCCTGGAGGTGC[C/T]GGGACCTCTGAACGA	10025
rs564990805	snp	A/G	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:874298	TTTGTATTTTTAGTA[A/G]AGACGGGGTTTCACC	10025
rs565012353	snp	C/T			intron-variant	MED16	GRCh38.p7	19:870326	AGCACTTTGGGAGGG[C/T]GAGGCAGGTGGATCA	10025
rs565013492	snp	C/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:887777	GACACAGAAGGCTAC[C/G]CAGTGTGTGATCCTG	10025
rs565131139	in-del	-/G	0.00279162	0.0372561	upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:893323	ATTTGGTAGAACAAC[-/G]AGCACTTTCTCAACT	10025
rs565136669	snp	C/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:871513	AGTATGTGGGAAGCA[C/G]TGTGCCTTTTCCAGA	10025
rs565230134	snp	A/C	0.00159617	0.0282053	intron-variant	MED16	GRCh38.p7	19:873977	GCTGGCAGCTGGCGG[A/C]GGTTACACACCCAAC	10025
rs565270807	snp	A/T	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:888675	CCATCCCGACAAAAC[A/T]GTTACCAAAAACAGG	10025
rs565284032	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:874834	GGGACTGCGTCACCG[C/T]GCTGCAACCTGGATG	10025
rs565303519	snp	A/G	0.00597247	0.0543191	intron-variant	MED16	GRCh38.p7	19:872308	GCTCAGAGCCCTGCA[A/G]GGCCCAGGACAGCCC	10025
rs565341621	snp	A/G	4.25876e-05	0.00461433	intron-variant	MED16	GRCh38.p7	19:868378	GCAGCTGGGCTCAGG[A/G]GTAGCTGAGGGGCAC	10025
rs565394968	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:870713	CCATGACTGGAGAAC[A/G]TGGAGGGAAGGAGCC	10025
rs565460469	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:874596	GCCTGCACAGGACCC[A/G]GGTGCCGGGTGTCGG	10025
rs565465637	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:870519	TGGGCCAAGACGGCA[C/T]TACTGCACTCCAGCC	10025
rs565552344	snp	A/G	0.00358779	0.0422022	intron-variant	MED16	GRCh38.p7	19:882567	GAGAGCACGTGTGGG[A/G]GGTCCTGCTGTGGCT	10025
rs565552453	snp	G/T	0.257176	0.249897	intron-variant	MED16	GRCh38.p7	19:877891	CCCCTGGTTGTCAAT[G/T]CCCACCAGCCCCAGC	10025
rs565588976	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:882161	CCCCTGCGTGAAGAC[A/G]CAGCTCCTCCCAACA	10025
rs565629877	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:886465	GTGTGCGCAACGGGA[A/G]TCACCTCCCCTTTCT	10025
rs565684173	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:873202	GGGCTAGGAAGTGGG[A/G]GTTTAAGAAGAGACA	10025
rs565692937	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	MED16	GRCh38.p7	19:894206	ATGCCCAACAAATTC[C/T]TGTATTTTTAGTAGA	10025
rs565713710	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:889919	GAGGTCTCGGCCCAG[A/G]TAGGGCACAGCAGGT	10025
rs565762994	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:893474	TAGCTGGTGGTGGAA[C/T]TCAATATTCGTGCTC	10025
rs565778615	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, downstream-variant-500B	MED16, RNU6-9	GRCh38.p7	19:893714	GCGATTCTCCTGCCT[C/T]AGCCTCCCGAGTAGC	10025
rs565834471	in-del	-/CTGTGTGCGCGCACGCCCGTGTGTGGGC	0.00835141	0.0640778	intron-variant	MED16	GRCh38.p7	19:877278	GGCACGTGTGTGGAT[-/CTGTGTGCGCGCACGCCCGTGTGTGGGC]CTGTGTGCGCGCATG	10025
rs565933017	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:880884	GAGCCGAGATCACAC[C/T]ACTGCACTCCAGCCT	10025
rs565935056	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:875754	AGTAACGGGTGGAGG[C/T]TGGGGAGGCTGCTCA	10025
rs565949038	snp	A/G			intron-variant	MED16	GRCh38.p7	19:891189	CGTCTATGTTGGCTG[A/G]GCACCCAGGGCATGT	10025
rs565965331	snp	C/T	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:883993	CACCTTTACTGCCTC[C/T]GCGGCCACAATGGGC	10025
rs566176846	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:876702	CCCAACCTGCCGCAG[A/G]GAAACCCCTCCAGCT	10025
rs566258466	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:883067	CCACACCCCCAGCTA[A/G]TGGCCAGGGTACCCT	10025
rs566295483	snp	C/T			intron-variant	MED16	GRCh38.p7	19:884372	GGGGGGCCCATCGGG[C/T]GGATAGAGATGGGAA	10025
rs566320380	snp	A/C			intron-variant	MED16	GRCh38.p7	19:869240	GGGACGAGGGTCGGT[A/C]CGCCACGTGCCCGGG	10025
rs566365814	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:885209	GAACGCAAATGTCCC[C/T]GGATGGTGCCCTCCC	10025
rs566432757	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:891443	AACAGACCATGGGGG[C/T]CAAGGGCACAGCCGG	10025
rs566444855	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:874928	AGCACTTTAGGAGGC[C/T]GAGGCGGGCGGATCA	10025
rs566458759	snp	A/G	8.8881e-05	0.00666578	intron-variant	MED16	GRCh38.p7	19:871907	GGGGAGAGGGGAGGG[A/G]CGGGCGGGGGTGCCT	10025
rs566654210	snp	A/C	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:877576	ACAAGGCAGCGCAGG[A/C]AGGGGCTGGCGAGGG	10025
rs566679980	snp	A/G			intron-variant	MED16	GRCh38.p7	19:873975	CGGCTGGCAGCTGGC[A/G]GCGGTTACACACCCA	10025
rs566741643	snp	C/G	0.000399281	0.0141238	downstream-variant-500B	MED16	GRCh38.p7	19:867568	GCTAAGCAACCTCCA[C/G]CAGAGAGCAGCTGGA	10025
rs566807417	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:891920	TGTGGCCGAGGCGGG[A/G]CTGAGTGTGATGGGG	10025
rs566871361	snp	C/T	0.00914312	0.0669923	intron-variant	MED16	GRCh38.p7	19:883286	GGGCATGGCGGGGAC[C/T]GAAGCCTGGCATGGT	10025
rs566874451	snp	C/T	0.0023933	0.0345097	intron-variant	MED16	GRCh38.p7	19:877554	ACAAGACGAACCCAT[C/T]ACACAGACAAGGCAG	10025
rs566908884	snp	A/G	0.0023933	0.0345097	intron-variant	MED16	GRCh38.p7	19:885549	GGCTGCGCTGTGGCC[A/G]CGAAGCGGGAGGAAG	10025
rs566914776	snp	A/C	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:881123	GGGCCTGAGCTAGGG[A/C]CGACTTGTCCACATT	10025
rs566951368	in-del	-/G	0.00119737	0.0244387	upstream-variant-2KB	MED16	GRCh38.p7	19:894177	GTAGCTGGGACTACA[-/G]GGCGCGCACCACCAT	10025
rs566998237	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:888757	CCGTGGCACGAAGCC[A/G]GTGCTGCGTGTACTG	10025
rs567011301	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:889129	AACTGTCCCCAACCC[C/T]GGCCACGCCTACTCT	10025
rs567076848	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:870205	CATCCAGGGGGGCCA[A/G]AGACTAAGGGCAGAG	10025
rs567249763	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:881360	TGTCTGCCAGCCTCA[C/T]AGATCCCGAAAGATG	10025
rs567293472	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:868799	CGCTGGGTGGGGGCT[A/G]GAATCAGCTGAGCCA	10025
rs567308940	snp	C/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:890434	CAGGCCTGTGAGGCG[C/G]CACAACTGTGTCTTT	10025
rs567391797	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:887188	CTAAGTTACAAGTTA[A/G]AAAAAAACACTTCTT	10025
rs567447282	snp	C/T			intron-variant	MED16	GRCh38.p7	19:875927	GGAGAGCCTGTGCAA[C/T]GTAGGACACCCCATC	10025
rs567462178	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:868619	CACGCCTGCTCCCCA[C/T]GTCCCCACCTGCCAC	10025
rs567465747	snp	C/G/T	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	MED16, RNU6-9	GRCh38.p7	19:893489	CTCAATATTCGTGCT[C/G/T]GCTTCGGCAGCACAT	10025
rs567501144	snp	C/T	0.000399281	0.0141238	synonymous-codon, utr-variant-5-prime	MED16	GRCh38.p7	19:890213	GTCCCAGGGGTGCTC[C/T]GTGTCCAGGATGTGG	10025
rs567538298	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, downstream-variant-500B	MED16, RNU6-9	GRCh38.p7	19:893630	AGAAACGGAATCTTG[C/T]TCTGTTGCCCAGGCT	10025
rs567558638	snp	A/G	0.00159617	0.0282053	intron-variant	MED16	GRCh38.p7	19:869189	CCTGGGGAGCTTGAG[A/G]CTTAGAGACCCAGTA	10025
rs567568220	snp	C/T	0.00199481	0.0315187	downstream-variant-500B	MED16	GRCh38.p7	19:867724	ATAGAGACAGGCAGA[C/T]AACACACTGAAAGGC	10025
rs567588697	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:873789	CCCCCGGGGGCCGCT[A/G]TGCTCAGCACCAACC	10025
rs567696459	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:887633	ATCGCACCACTGCAC[C/T]CCAGCCCGGTTGACA	10025
rs567793288	snp	C/T	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:874345	TCTCGATCTCCTGAC[C/T]TCGTGATCAGCCCGC	10025
rs567816375	snp	C/T			intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:892637	AGTCCCCAGTCTCCA[C/T]CCTAGGGACCCTATT	10025
rs567831329	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	MED16	GRCh38.p7	19:894909	GCCAACATGTTGAAA[A/C]CACATCTCTACTAAA	10025
rs567856428	snp	A/G	0.0023933	0.0345097	intron-variant	MED16	GRCh38.p7	19:872538	ACAAAAAGAAGAGAG[A/G]GACTTCAAACCGTCC	10025
rs567894874	snp	C/T	0.000399281	0.0141238	synonymous-codon	MED16	GRCh38.p7	19:875383	GGTGTGGTAGTCGCA[C/T]ACGCGGGTCACCGTG	10025
rs567931589	snp	A/G			intron-variant	MED16	GRCh38.p7	19:873829	CGGCCTGCAGGCCTT[A/G]GCGTGGGCAGGTCCC	10025
rs567958468	snp	C/G	6.3998e-05	0.0056564	missense, intron-variant	MED16	GRCh38.p7	19:877159	GGTGGCCCATGGAAG[C/G]TGAGAGGCGGAGCAC	10025
rs568046830	snp	A/G			intron-variant	MED16	GRCh38.p7	19:886734	ATTTGTCAAGTCATT[A/G]TTGACATACGGAAAC	10025
rs568065755	snp	G/T			intron-variant	MED16	GRCh38.p7	19:872207	GGTGGAACCCCGACC[G/T]GGGGGCAATGGGCAG	10025
rs568096456	snp	C/G	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:893196	GTCGCCTGAGGCGTG[C/G]GGCCGCCTCCCAAAG	10025
rs568145217	in-del	-/GCGCCCCGCGCCCCGCGCCCC			intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:892922	CGCGCCCCGCGCCCC[-/GCGCCCCGCGCCCCGCGCCCC]AGGCCGCCTACCCAG	10025
rs568267309	snp	C/G	0.290718	0.246662	intron-variant	MED16	GRCh38.p7	19:879820	GTCAATCCCCACCAG[C/G]GCCAGCCCCACGTGC	10025
rs568311248	snp	C/T	3.93074e-05	0.00443308	missense	MED16	GRCh38.p7	19:880014	AGTGGACGGCGGGGC[C/T]CGCGGTGCGGGGGCG	10025
rs568342317	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:876624	CTCTGGGAGCACACC[C/T]CACACGCAGCCTCAC	10025
rs568350965	snp	A/G	0.00835141	0.0640778	intron-variant	MED16	GRCh38.p7	19:883459	AGCTGGGCATGGCGG[A/G]GACCAAAGCCTGGCA	10025
rs568438330	snp	C/T	0.000399281	0.0141238	missense, utr-variant-5-prime	MED16	GRCh38.p7	19:886188	AACTTCTCCCCGAAG[C/T]TGGAGGCGCCCGACT	10025
rs568489857	snp	A/T			intron-variant	MED16	GRCh38.p7	19:873888	GGCCTGCTGGTGCAC[A/T]TCTGCCCCCTGCTCC	10025
rs568508861	snp	G/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:876268	CCTTCGAGGACACTC[G/T]GGGATTGCAGGCACA	10025
rs568543917	snp	A/G	0.00159617	0.0282053	intron-variant	MED16	GRCh38.p7	19:880594	AGCCCAAAGCTCATG[A/G]AAAAGAGAATATGAA	10025
rs568557141	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:880285	CCAATCGGCATCCAG[C/T]GCCCGTGCCCCCAGC	10025
rs568567895	snp	A/G	0.00199481	0.0315187	intron-variant	MED16	GRCh38.p7	19:876358	CTCCTTCCGACGGGC[A/G]GGTCTCTGTGTGTTC	10025
rs568700465	snp	C/T	2.3127e-05	0.00340044	missense	MED16	GRCh38.p7	19:884936	GGAAGATGTTGTTCA[C/T]GGGGAGTCCCTCCTT	10025
rs568781178	snp	A/G	9.78202e-05	0.00699289	intron-variant	MED16	GRCh38.p7	19:868254	GCCTTCAACAGCCCT[A/G]CAGGGCGGGCTGAGG	10025
rs568815992	snp	C/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:878082	GGCTGTCAATGCCCC[C/G]CAGCCCCAGCCCCAG	10025
rs568827185	snp	A/C	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:887551	CGTGCCTGTAATTCC[A/C]GCTACTCGGGAGGCT	10025
rs568942055	snp	A/C	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:877549	GCTCAACAAGACGAA[A/C]CCATCACACAGACAA	10025
rs569008857	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:874562	CCCCTTACGGCAAAA[C/T]GGAAGGAGGAGCAGA	10025
rs569025712	snp	A/G	0.000118966	0.00771159	intron-variant	MED16	GRCh38.p7	19:881717	TGTTTGTCGCCAACT[A/G]AAAAATCAGGGGCAG	10025
rs569057781	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	MED16	GRCh38.p7	19:867617	AGTCAGGCAGAGACA[C/T]AGAAACAGCATGCAG	10025
rs569060162	snp	C/T	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:884748	GCGCGCGGTCACACC[C/T]GAGATCCTAGCACTA	10025
rs569093471	snp	C/T			synonymous-codon, utr-variant-5-prime	MED16	GRCh38.p7	19:890180	GGCCTCGTGGTGCTC[C/T]GAGGGGATCGAGTGC	10025
rs569105598	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:869035	CAGGCGGGGGTGGAG[A/G]GAATGGCCGGCCTCA	10025
rs569158702	snp	A/G			upstream-variant-2KB, nc-transcript-variant	MED16, RNU6-9	GRCh38.p7	19:893541	AGAGAAGATTAGCAT[A/G]GCCCCTGCGCAAGGA	10025
rs569295652	in-del	-/CCC	0.00329082	0.0404299	intron-variant	MED16	GRCh38.p7	19:889152	CCTACTCTTAACTGT[-/CCC]CCCCAACCCTGGCCA	10025
rs569302783	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:885532	ATTCAGAGACAGGAA[A/G]AGGCTGCGCTGTGGC	10025
rs569371325	snp	A/G			upstream-variant-2KB	MED16	GRCh38.p7	19:895043	GTGAGCTGAGATCGC[A/G]CCACTGCACTCCAGC	10025
rs569381509	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:869895	GGCCACTTCCTGACC[A/G]CGTGACCCCAGATGA	10025
rs569385152	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:891661	GTGGCCGAGGCGGGG[G/T]CTGAGTGTGACGGGG	10025
rs569389269	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:885330	CGACCTGGTGTGGTC[A/G]GCTCAACAGTGGCCC	10025
rs569574521	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:871754	GACTTGTGTTTTGGT[A/G]GGGAGAGGGGAGCGG	10025
rs569612290	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:874619	GGTGTCGGCCTGGGA[A/G]CGTCTCAGCCCCCAG	10025
rs569620954	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:884005	CTCTGCGGCCACAAT[A/G]GGCAGTTGACATAAC	10025
rs569627639	in-del	-/T	0.0107246	0.0724382	intron-variant	MED16	GRCh38.p7	19:869605	GCACGAGGAAGAAAA[-/T]TGCTGGAGGTCCTAG	10025
rs569665012	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:890714	GCCTCCGTCAACCAA[C/T]GCTCCAGCCCGATTC	10025
rs569675678	snp	A/G	0.00358779	0.0422022	intron-variant	MED16	GRCh38.p7	19:870973	CGTGTGGATTCGGGG[A/G]TCCCGGGGCAGGACA	10025
rs569802849	snp	A/G	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:884783	AGATCGAGGCGAGAC[A/G]ATCGCTTAGGGCCGG	10025
rs569882168	snp	C/T	0.0146672	0.084371	intron-variant	MED16	GRCh38.p7	19:873241	AAGTGGGACTCCAAG[C/T]AGGGGTGGGACTCCA	10025
rs569890852	snp	G/T	0.152778	0.230321	intron-variant	MED16	GRCh38.p7	19:872946	AGGAGGGCTCCGAGG[G/T]GGGGGAGGGCTCCGA	10025
rs569963957	snp	A/G	0.000390533	0.0139683	intron-variant	MED16	GRCh38.p7	19:871571	ACCCTCCTCACATAC[A/G]CACAACCCGACAAGG	10025
rs569978643	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:876799	GGGAACTCCCTCCCT[A/G]CTGCTGGCACTTTAC	10025
rs570043273	snp	C/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:868851	GAGTCAGCGGTTCCG[C/G]GGGCCCCTCACCTGG	10025
rs570098209	snp	G/T			upstream-variant-2KB	MED16	GRCh38.p7	19:894326	GGCGTGAGCCACCGC[G/T]CCCAGCCTGTTTTTT	10025
rs570110025	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	MED16	GRCh38.p7	19:894315	CTGGGATTACAGGCG[C/T]GAGCCACCGCGCCCA	10025
rs570216219	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:881338	ACATATTAAAGAACA[C/T]TGGATCTGTCTGCCA	10025
rs570278624	snp	A/G	0.0023933	0.0345097	intron-variant	MED16	GRCh38.p7	19:870602	AGAGGGTGAATGGAA[A/G]GGCTGGGTGCCCGTG	10025
rs570334995	snp	C/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:881028	TCTGCAGGCTCTGAG[C/G]AACAGCCCTGAGCCC	10025
rs570403252	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:872215	CCCGACCGGGGGGCA[A/G]TGGGCAGGGTCTGGG	10025
rs570416876	snp	C/G			intron-variant	MED16	GRCh38.p7	19:887753	CATCACGCTCAGTAA[C/G]AGATGCCAGACACAG	10025
rs570429772	snp	C/G			intron-variant	MED16	GRCh38.p7	19:886429	CTTTAGAGGACAGTG[C/G]GGAGGATTAAACGGG	10025
rs570487109	snp	G/T			intron-variant	MED16	GRCh38.p7	19:870981	TTCGGGGGTCCCGGG[G/T]CAGGACACGGAGGAA	10025
rs570669644	in-del	-/G			intron-variant	MED16	GRCh38.p7	19:872609	TGAAGCCGGGTGGGT[-/G]GGGCAGAAGAAATCA	10025
rs570691719	snp	A/G	0.00199481	0.0315187	intron-variant	MED16	GRCh38.p7	19:882694	GGGAACCAGGAGAGC[A/G]CAGCTGAGGCAGCCA	10025
rs570728238	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:885477	TCCGGGGGCCCCAGT[A/G]TCCTCACAGGGTCCT	10025
rs570740335	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:889490	ACTGAACACACAGGT[A/G]CTAATGACAGCCGGA	10025
rs570834876	snp	C/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:875842	GGAGACCCTGGTCTA[C/G]AGAGAATGAATGAAT	10025
rs570836872	snp	A/C	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:880559	CCATTGTACGAGGGC[A/C]GGGGGGAGGTGGGGT	10025
rs570922221	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:880219	GGGAGGGGCCTCCTG[C/T]TCTGCAGGGTGTGGA	10025
rs570929892	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:883417	ACCGAAGCCTGGCAC[A/G]GTGGGCACGTGGGGC	10025
rs571122682	snp	C/T	3.71872e-05	0.00431187	utr-variant-3-prime	MED16	GRCh38.p7	19:868066	AGGAGACGCCCGAGC[C/T]GGGTCACCACAAGGT	10025
rs571149157	snp	A/C/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:870230	GCAGAGGCTAAGGCA[A/C/G]GGCGCCCTGTACAGC	10025
rs571153849	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:890690	AACTGGGGCACGTGT[C/T]TCCAACAAGCCTCCG	10025
rs571260352	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:877363	AGGGTCATGCACAAT[A/G]CCTCTGGGAACAGGG	10025
rs571275676	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:884708	GGAGGAGTCTATACG[C/T]CTAACACACTCAGAA	10025
rs571311198	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	MED16	GRCh38.p7	19:867589	AGCAGCTGGAGAAAC[A/G]TAACAGGGACAGAGT	10025
rs571343436	snp	A/G	0.0023933	0.0345097	intron-variant	MED16	GRCh38.p7	19:869136	CCCAGTAAAGGGGGC[A/G]GGACCCCCCACACGG	10025
rs571447898	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:887260	CCTGGTGGTGAGGGG[C/T]TGCCATGGCGACGAC	10025
rs571471124	snp	A/C	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:869019	CAGGGGCATCTGTCC[A/C]CAGGCGGGGGTGGAG	10025
rs571501870	snp	C/T	0.0134861	0.0810011	intron-variant	MED16	GRCh38.p7	19:891273	GCCGATGCAAAGGCC[C/T]GGAGGCCAGACAGAG	10025
rs571543405	snp	A/G	0.00159617	0.0282053	intron-variant	MED16	GRCh38.p7	19:880829	GGGAGGCTGAGGCAG[A/G]AAGGAGAATCGCTTG	10025
rs571544013	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:885271	GTCAGGGGCTTCAAG[A/G]AGTTTGGGGCGTTAC	10025
rs571667156	snp	A/C	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:883491	GGTGGGCACGTGGGG[A/C]GGTAGGGGGAGAGAT	10025
rs571696626	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:888349	CAACATGGTGAAACC[C/T]CGTCTCTACTAAAAA	10025
rs571731839	snp	A/C	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:887955	CGCCTGTCATCCCAG[A/C]ACTTTGGGAGGCCAA	10025
rs571760467	snp	A/G	0.0166325	0.0896639	intron-variant	MED16	GRCh38.p7	19:871831	GGAGAGCGGGGAGAG[A/G]GGAGAGCGGGGAGAG	10025
rs571846344	snp	C/G/T	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:887389	AAACAAAAATTTGGC[C/G/T]GGACGCGGTGGCTCA	10025
rs571870528	snp	A/G			intron-variant	MED16	GRCh38.p7	19:882955	CCCAGAGGGCACACA[A/G]TGGTCAGGGGTGGCT	10025
rs571900328	snp	C/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:870352	GATCACCTGAGGTCA[C/G]GAGTTCAAGACCAGC	10025
rs571919378	snp	G/T	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:874132	CTAAATTTTTTTTTT[G/T]AGACAGAGTCTCACT	10025
rs571979608	snp	A/C	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:877503	AGTTACGAAGCTCCT[A/C]ATACGTGCTGTGAGC	10025
rs572020782	snp	C/T	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:872304	CGCTGCTCAGAGCCC[C/T]GCAGGGCCCAGGACA	10025
rs572099180	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:885675	CACCACGGTTTAGCC[C/T]GTGGAGGCCCGCGCG	10025
rs572122997	snp	C/T	1.66957e-05	0.00288922	missense	MED16	GRCh38.p7	19:885888	ATCTCCGTGTCGATA[C/T]GGCACTTCTCGCTCA	10025
rs572136187	snp	A/G	0.0023933	0.0345097	utr-variant-3-prime	MED16	GRCh38.p7	19:867974	GGCCTGGGCGCAGAG[A/G]GCGTTTATTGGACCT	10025
rs572148659	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:890066	GACTCCAGACTGACC[A/G]GAGAAACACAGGGCC	10025
rs572188943	snp	C/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:888885	TTCCTGCGAGAGCCC[C/G]AGCACAAGCAGACGC	10025
rs572276685	snp	G/T			upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:893372	AGTTGCATTACACAT[G/T]GGGCTAATATAAATA	10025
rs572352451	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:892136	CCTGGCATCCAGACG[A/G]GCTGTTTCGCTTCGC	10025
rs572359685	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:886673	ACTCAGGAAGTGCTG[C/T]GTAAGCACCAGCGGC	10025
rs572460757	snp	G/T	0.0158469	0.0875917	intron-variant	MED16	GRCh38.p7	19:873362	GCGGGGCTGAGGTGG[G/T]TTTGAGGGGCAGGGG	10025
rs572584095	snp	C/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:870622	GGGTGCCCGTGTTGG[C/G]GGTGGTTCGTGACAC	10025
rs572600520	snp	A/G	0.00358779	0.0422022	intron-variant	MED16	GRCh38.p7	19:873063	CCGAGGTGGGGCAGG[A/G]CTCCGAGGTGGGGGA	10025
rs572634946	snp	C/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:875992	GAAACGCTTGGCACA[C/G]AGCGACGGCCCAAGG	10025
rs572757509	snp	C/T	1.75188e-05	0.00295958	intron-variant	MED16	GRCh38.p7	19:891180	GTGGTGGGACGTCTA[C/T]GTTGGCTGAGCACCC	10025
rs572866974	snp	C/T	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:869343	TCCACACCACCTCTG[C/T]CCAGACACCCGGCCT	10025
rs572890018	snp	C/T	1.79877e-05	0.00299892	intron-variant	MED16	GRCh38.p7	19:890925	CAGGGCGGGACACCA[C/T]GCGGCCGGGAGGGGA	10025
rs572902608	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:874433	TTTTAAAAGAAACAG[C/T]CTGCCAGGCACAGTG	10025
rs572946175	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:871763	TTTGGTAGGGAGAGG[A/G]GAGCGGGGAGAGGGG	10025
rs572950494	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:874239	CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC	10025
rs572989873	snp	G/T	0.00279162	0.0372561	intron-variant	MED16	GRCh38.p7	19:877403	TCCCTGAGCCCCGAC[G/T]GCACTGGATGCCGAG	10025
rs573058279	snp	C/T			intron-variant	MED16	GRCh38.p7	19:891323	GGGAACATGGAGAGG[C/T]CAGGGCCAGTCCTGG	10025
rs573115767	snp	C/T	0.105569	0.204058	intron-variant	MED16	GRCh38.p7	19:877295	GTGTGCGCGCACGCC[C/T]GTGTGTGGGCCTGTG	10025
rs573187348	snp	A/C	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:875051	TGCCTGTAATCCCAG[A/C]TACTTGGGAGGCTGA	10025
rs573190828	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:874809	CAGAAGGCAGAGGCT[A/G]CGCTGAGCTGGGACT	10025
rs573399068	snp	C/T	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:882814	GCTCTGTGCCACCCG[C/T]ATCATGAGGTCTCTG	10025
rs573448989	snp	A/G	0.0023933	0.0345097	downstream-variant-500B	MED16	GRCh38.p7	19:867666	CAGAGAAGTGCAGAG[A/G]TACCAGAGACACGCA	10025
rs573502045	snp	C/G			intron-variant	MED16	GRCh38.p7	19:876275	GGACACTCTGGGATT[C/G]CAGGCACATAACCAC	10025
rs573523766	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:885423	CTGCGGGTGGGATTC[A/G]GTTCGGGACACTGAG	10025
rs573562486	snp	C/T	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:885082	CCGGAGCCTGAGCTG[C/T]GGGACCCTGGGGCCA	10025
rs573613034	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:876529	TCAGGCCTTACCTGT[A/G]GGGCTTAACGTGTTA	10025
rs573655336	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:884769	CCTAGCACTACTGGA[A/G]ATCGAGGCGAGACGA	10025
rs573659519	snp	C/G	0.00159617	0.0282053	intron-variant	MED16	GRCh38.p7	19:881462	CAGAGCCCACGTCCT[C/G]TGGTGTGAGCTCCCA	10025
rs573698868	snp	C/T	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:880749	ACACCGGTGAAACCC[C/T]GTCTCTACTAAAATA	10025
rs573742934	snp	A/G	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:884616	CCTCACGGTGTCCCC[A/G]CTGGCTGAGCAACGA	10025
rs573840027	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:890049	CTCTAGACCCAGCGC[C/T]GGACTCCAGACTGAC	10025
rs573843087	snp	A/C	0.00199481	0.0315187	intron-variant	MED16	GRCh38.p7	19:883860	AGGAATGAGGCCCAA[A/C]AAGGCCCTGGGGACC	10025
rs573856866	snp	C/G	0.000798403	0.0199641	upstream-variant-2KB, downstream-variant-500B	MED16, RNU6-9	GRCh38.p7	19:894074	AGGGTCTCGCTCTGT[C/G]GCCCAGGCTGGAGTG	10025
rs573859172	snp	A/G			intron-variant	MED16	GRCh38.p7	19:876418	CACCACAGGGCCACC[A/G]GGTGTGCATCCTGGT	10025
rs573901658	snp	A/C/G	3.83156e-05	0.0043768	intron-variant	MED16	GRCh38.p7	19:871590	AACCCGACAAGGAGA[A/C/G]ACAGCAAACAGGTGC	10025
rs573965002	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:886291	GCACAGAAGAACCAC[A/G]CAGAAGCCAGGAGTG	10025
rs573965997	snp	C/T	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:881774	ACAGGCTGAGACAGC[C/T]GCAGGAGTCCAGCAT	10025
rs573976856	snp	A/G	0.00398564	0.0444627	intron-variant	MED16	GRCh38.p7	19:869101	AGTGAGGTGGGAGGT[A/G]CGGGACCACCTGAGA	10025
rs574003652	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:873652	CTAACTGCACCCCTC[A/G]GTCCTTCGACCTGCA	10025
rs574080336	snp	A/G	0.000181274	0.00951863	missense	MED16	GRCh38.p7	19:868915	CAAGGTGCAGCCTCC[A/G]CAGGTGGTCGATCTT	10025
rs574122502	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:890564	TTTCTGTGGTTTTCT[A/G]GTTTTCTCTAATGAC	10025
rs574143789	snp	A/C	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:885626	AGAAAATGGGTTCTC[A/C]CCTGGAGCCCCCGGG	10025
rs574169594	snp	A/C	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:868735	TGGGATCCTGGCTCC[A/C]ACACTCCCTCTGGGA	10025
rs574182895	snp	C/T	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:888790	GCAATGCGCCGACAA[C/T]GGCAGTCCCTGGGGA	10025
rs574259177	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:883737	CCCAGCGGGGGCACC[A/G]GGCAGTGAAGGTGCA	10025
rs574267294	snp	A/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:888628	GTGTGGGCTGCACAC[A/T]CTCAATGGGTGAGTT	10025
rs574292816	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	MED16	GRCh38.p7	19:894383	ACTATGTTGCCCAGG[C/G]TGATTTCAAACTCCA	10025
rs574292849	snp	C/T			intron-variant	MED16	GRCh38.p7	19:875102	CAGAGAGGCGGAGGC[C/T]GCAGTGAGCTGAGAT	10025
rs574382686	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, downstream-variant-500B	MED16, RNU6-9	GRCh38.p7	19:893846	CTGATCCGCCCGCCT[C/T]GGCCTCCCAGAGTAC	10025
rs574431819	in-del	-/GGGAAGAACGGGAGCTGG	0.00318978	0.0398085	intron-variant	MED16	GRCh38.p7	19:881080	CTTTCCAGGGAACCA[-/GGGAAGAACGGGAGCTGG]GGGAAGAACGGGAGC	10025
rs574480161	snp	A/G	0.000798403	0.0199641	downstream-variant-500B	MED16	GRCh38.p7	19:867717	AGACAGTATAGAGAC[A/G]GGCAGACAACACACT	10025
rs574541267	snp	C/T	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:869746	CACTTCATTTTCTTC[C/T]TTTTGCTCATCTGTG	10025
rs574557479	snp	A/G	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:891492	TGCGCTGGCCCAGGT[A/G]AGTGATGATGGGGGC	10025
rs574625488	snp	A/G			intron-variant	MED16	GRCh38.p7	19:869811	TCAGAGGGTTTGCAT[A/G]TGCTCCTTGTCAAAC	10025
rs574718927	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:870093	TGACCTCTTGCCCCC[A/G]GGAGATCCTCCTGAT	10025
rs574756112	in-del	-/T	0.00318978	0.0398085	upstream-variant-2KB, nc-transcript-variant	MED16, RNU6-9	GRCh38.p7	19:893537	TACAGAGAAGATTAG[-/T]CATGGCCCCTGCGCA	10025
rs574784238	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:893384	CATTGGGCTAATATA[A/C]ATAGAGGTTAAATCT	10025
rs574814420	snp	A/C	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:883056	TGCCATGACGACCAC[A/C]CCCCCAGCTAGTGGC	10025
rs574844967	snp	A/G			intron-variant	MED16	GRCh38.p7	19:888619	CTCTGGACCGTGTGG[A/G]CTGCACACTCTCAAT	10025
rs574908112	snp	A/G			intron-variant	MED16	GRCh38.p7	19:890556	ATTCCAATTTTCTGT[A/G]GTTTTCTAGTTTTCT	10025
rs574940998	in-del	-/GG/GGGGCACAGGCACTGCTTAGACATGGGC	0.00275811	0.0370331	intron-variant	MED16	GRCh38.p7	19:880152	CAGGGCCAGCCCTGT[lengthTooLong]GGGGCACAGGCACTG	10025
rs574956981	snp	C/G	0.0696718	0.173152	intron-variant	MED16	GRCh38.p7	19:873059	GGCTCCGAGGTGGGG[C/G]AGGGCTCCGAGGTGG	10025
rs574993649	snp	A/G	0.00835141	0.0640778	intron-variant	MED16	GRCh38.p7	19:872765	ACCCCAGGCGCAGGG[A/G]GCTGGGGAGGGTAAG	10025
rs575028234	snp	C/T			intron-variant	MED16	GRCh38.p7	19:874171	CAGGCTGGAGTGCAG[C/T]GGGGTGATCTCAGCT	10025
rs575080791	snp	A/C/T	0.00159617	0.0282053	intron-variant	MED16	GRCh38.p7	19:875535	AGGAGAAGAGCAGTT[A/C/T]GACTCTGACACCAGG	10025
rs575296477	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB	MED16	GRCh38.p7	19:894650	TTTAACGTTCTTAGC[A/G]GCCCGGGTGTGGTGG	10025
rs575334601	snp	C/T			intron-variant	MED16	GRCh38.p7	19:886767	CCACCCTTCTTTCAA[C/T]GTGAGTCTTTTAAAA	10025
rs575378759	snp	A/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:881402	CTAATTGGGAACCCA[A/T]CAGAACCCAGAAGGC	10025
rs575464439	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:884525	GCACCGCCCCTGCCC[A/G]GTCTGGCCTGTCCCC	10025
rs575501816	snp	C/G/T	0.00122766	0.024746	intron-variant	MED16	GRCh38.p7	19:877225	GGTGAGATGGGGCTG[C/G/T]GCCCTCAGCCGGGAG	10025
rs575582411	snp	C/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:877716	CAATGCCCACCAGCC[C/G]CTGCCCCACGTGCCC	10025
rs575583224	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:892793	AGCGCCTTCAGCCTC[A/G]CCCCAAACTCTCCTT	10025
rs575622227	snp	C/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:882495	CGCCACTGCACTCCA[C/G]CCTGGGCAACACAGC	10025
rs575625701	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:876038	TCTCGCCATCACTAG[C/T]GCTGTCACTGGCTAC	10025
rs575662410	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:880434	CGCCCCTCAAGGAGC[A/G]CAGGGGAGGGGGGCA	10025
rs575695913	in-del	-/GCA	0.00478085	0.0486577	upstream-variant-2KB	MED16	GRCh38.p7	19:894856	GGGAGGCTGAGGCAC[-/GCA]GCAGATCACCTGAGA	10025
rs575732412	snp	A/G	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:876218	GAGGGCTGGTCCCAC[A/G]TGCAGCTGCCGGCTG	10025
rs575843847	snp	C/T	0.000135906	0.00824226	intron-variant	MED16	GRCh38.p7	19:868275	CGGGCTGAGGTTAAC[C/T]GCGCCGAGGAGAGTC	10025
rs575866495	snp	A/C/T	0.000682436	0.0184604	intron-variant	MED16	GRCh38.p7	19:885059	CTGCTGTGGTGGCCA[A/C/T]GCCACCACCGGAGCC	10025
rs575880288	snp	A/G	1.69496e-05	0.0029111	utr-variant-5-prime	MED16	GRCh38.p7	19:891142	CACATGAGGGCAGTC[A/G]CCAGCTCCTGCGGGA	10025
rs575881716	snp	A/G/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:869103	TGAGGTGGGAGGTGC[A/G/T]GGACCACCTGAGACA	10025
rs575915108	in-del	-/GCAGAGACACAGAAACAGCAT	0.00557542	0.0525036	downstream-variant-500B	MED16	GRCh38.p7	19:867608	CAGGGACAGAGTCAG[-/GCAGAGACACAGAAACAGCAT]GCAGAGACACAGAGA	10025
rs575941403	snp	C/T	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:880690	TTTGGGAGGCTGAGG[C/T]GGGCAGATTGCCTGA	10025
rs575957412	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:884829	TGGGTGACACAGCAA[A/G]ACCTGCCTCCAAAAT	10025
rs575982170	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:887298	GTGTCCACACCACAC[A/G]TCTGTGTGGGTCGCA	10025
rs576067300	snp	A/G	0.0422008	0.138995	intron-variant	MED16	GRCh38.p7	19:887097	AAACAAAAAAAAAAA[A/G]AACAAGAAAAATGTC	10025
rs576101045	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:883525	GGAGAGATGGGTGCG[A/G]TGGGGACTGTCCCAG	10025
rs576104521	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:890316	GATGACTCCAGGCAG[A/G]CTCCAGGTAAGCCGG	10025
rs576230329	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:870573	CGGGGAGACAAAAAA[A/G]AAAAAAAAAAGGGAG	10025
rs576234327	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:893319	CTATATTTGGTAGAA[A/C]AACGAGCACTTTCTC	10025
rs576294727	snp	C/T	0.0023933	0.0345097	intron-variant	MED16	GRCh38.p7	19:873386	GCAGGGGCAGGGAAG[C/T]GGGGTCCTGATGAGA	10025
rs576320746	snp	A/C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:870416	AAATACAAAAAATAC[A/C/T]TAGGTGTGGTGGCTC	10025
rs576338942	snp	A/C	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:884174	TGTGCTCTCATCTAC[A/C]GGGAAAACATCTCCC	10025
rs576431511	snp	C/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:868662	CATGCTTCTCCTCCC[C/G]CCAGCAATGCTGCTC	10025
rs576469093	snp	C/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:888558	AGATAAAGGTCTGAG[C/G]TTAGCTATGGTGGTG	10025
rs576500969	snp	C/G	0.000134944	0.00821302	synonymous-codon	MED16	GRCh38.p7	19:871060	GCCGTCGAGCTGCAG[C/G]GTGGCAGCACTGCCA	10025
rs576558528	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:870868	TGGAGGGAGGGAGCC[A/G]TGTGGATTCGGGGGG	10025
rs576577904	snp	C/T	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:882152	GCCTGACAGCCCCTG[C/T]GTGAAGACGCAGCTC	10025
rs576592674	snp	A/C	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:891193	TATGTTGGCTGAGCA[A/C]CCAGGGCATGTGGAG	10025
rs576619447	snp	A/G			intron-variant	MED16	GRCh38.p7	19:869713	GGGGCCTTCCCCGGA[A/G]CAGGGCTGCTGGAGG	10025
rs576728498	snp	A/G	0.00398564	0.0444627	intron-variant	MED16	GRCh38.p7	19:877617	GTGGTCCCTTCCCCC[A/G]GGGGCGCCTCCCTCT	10025
rs576891215	snp	A/C			intron-variant	MED16	GRCh38.p7	19:868757	CCTCTGGGACGTGCT[A/C]CCTCCACCACCCTTG	10025
rs576908813	snp	A/G	7.29474e-05	0.00603891	synonymous-codon	MED16	GRCh38.p7	19:871957	GGTGAGCAGGCGGAA[A/G]AGCAGGGACATGCTG	10025
rs576938391	snp	C/G	0.00755907	0.0610114	intron-variant	MED16	GRCh38.p7	19:871768	TAGGGAGAGGGGAGC[C/G]GGGAGAGGGGAGAGG	10025
rs577113248	snp	C/T			intron-variant	MED16	GRCh38.p7	19:883653	GACGGCTGCAGGAGA[C/T]GAGGAGGAGTGTCGG	10025
rs577126879	in-del	-/CTGG	0.00279273	0.0372635	intron-variant	MED16	GRCh38.p7	19:871429	CCCGGCTCTGCCTGC[-/CTGG]CTGGGTGACCCCAGA	10025
rs577186584	snp	A/G			intron-variant	MED16	GRCh38.p7	19:886989	GAGGCTGAGGCAGGA[A/G]AATTGCTGGAATCCA	10025
rs577232311	snp	C/T	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:872330	GGACAGCCCCATTTG[C/T]AGAGTCGTCCCATCC	10025
rs577273693	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:893006	CAGGCCCCGCCACGG[C/T]TGCGCCGCGTTCCCT	10025
rs577393244	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:882834	TGAGGTCTCTGCCCC[A/G]GACGGGCCATCACGG	10025
rs577417377	snp	A/G	0.000798403	0.0199641	intron-variant	MED16	GRCh38.p7	19:875139	ACTGCACTCCAGCCT[A/G]GGCAACAGAGTAAGA	10025
rs577484524	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:885567	AAGCGGGAGGAAGGC[A/G]CCCCGAACCGAGGGA	10025
rs577485739	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:882589	GCTGTGGCTGCATGT[A/G]GGACACGGAGGGCAG	10025
rs577502039	snp	A/C/T	0.000252625	0.0112363	intron-variant	MED16	GRCh38.p7	19:879911	AATGCCCACCAGCCC[A/C/T]GGCCCCACGTGCCCC	10025
rs577542024	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:873873	CCAGTGCTCAGGCCC[A/G]GCCTGCTGGTGCACA	10025
rs577580941	snp	A/G	0.0023933	0.0345097	upstream-variant-2KB	MED16	GRCh38.p7	19:894318	GGATTACAGGCGTGA[A/G]CCACCGCGCCCAGCC	10025
rs577631218	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:873690	CCCACCCAGTACCAG[A/G]ACACAAGGGGACCCA	10025
rs577641092	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:881775	CAGGCTGAGACAGCC[A/G]CAGGAGTCCAGCATG	10025
rs577711860	snp	A/G			intron-variant	MED16	GRCh38.p7	19:877800	CAGCCCCAGCCCCAC[A/G]TGCCCCAGCAGCTCG	10025
rs577809066	snp	C/T			intron-variant	MED16	GRCh38.p7	19:882812	CTGCTCTGTGCCACC[C/T]GCATCATGAGGTCTC	10025
rs577885905	snp	C/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:883879	GCCCTGGGGACCGGG[C/G]GAAGGAACGAGCCCT	10025
rs577891775	snp	A/G	0.00119737	0.0244387	downstream-variant-500B	MED16	GRCh38.p7	19:867506	CTGGAGACGGAAGGC[A/G]GGACCCCTGGGGACA	10025
rs578019444	snp	A/G	0.00597247	0.0543191	intron-variant	MED16	GRCh38.p7	19:868636	TCCCCACCTGCCACA[A/G]GGCCTCTGCCCATGC	10025
rs578046978	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:884787	CGAGGCGAGACGATC[A/G]CTTAGGGCCGGGGTT	10025
rs578077753	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:887693	TTTGGTTATTTTAAA[A/G]AGCGAGGCTCTGACT	10025
rs578155300	snp	A/G	0.000399281	0.0141238	intron-variant	MED16	GRCh38.p7	19:887406	GACGCGGTGGCTCAC[A/G]CCTGTAATCTCAGCA	10025
rs578178116	snp	A/C/G/T	0.000167578	0.00915238	intron-variant	MED16	GRCh38.p7	19:871643	AAGCACCCACACAGA[A/C/G/T]CATGGACCTGTGCTA	10025
rs578244913	snp	C/T	0.00119737	0.0244387	intron-variant	MED16	GRCh38.p7	19:890600	ATTATGAGTGCCTAT[C/T]ACTCAAACAATGGAG	10025
rs745332883	snp	A/G	6.50936e-05	0.00570461	intron-variant	MED16	GRCh38.p7	19:872165	CGGCGGGGGGCAGAT[A/G]GCGATGGGATGAAGT	10025
rs745397616	snp	C/G	1.69585e-05	0.00291187	intron-variant	MED16	GRCh38.p7	19:868505	ACAGCCGCACCTGCG[C/G]GGAGGCAGGCACTGA	10025
rs745399772	snp	C/G			intron-variant	MED16	GRCh38.p7	19:869490	TCTGAAATTTTCCCA[C/G]TTTACAAGCCTCTGA	10025
rs745416680	snp	C/T	4.00088e-05	0.00447245	missense	MED16	GRCh38.p7	19:880119	GGTGCACGATGTGGA[C/T]GCTGCCGTCGTGGAA	10025
rs745431954	snp	C/G	0.00102407	0.022605	intron-variant	MED16	GRCh38.p7	19:890289	CTGGCACCACAGCCT[C/G]CAGACGATGACGATG	10025
rs745438612	snp	A/G			intron-variant	MED16	GRCh38.p7	19:871517	TGTGGGAAGCACTGT[A/G]CCTTTTCCAGACACT	10025
rs745502020	snp	A/G	1.7192e-05	0.00293185	missense, intron-variant	MED16	GRCh38.p7	19:877093	AGCCGGTCACCATGC[A/G]GTACTCCAGCAGGAA	10025
rs745537969	snp	A/G	1.66776e-05	0.00288765	synonymous-codon	MED16	GRCh38.p7	19:873581	CATGACCTTGTCAAT[A/G]TCTACAAGGAGACGT	10025
rs745545558	snp	C/T	1.9888e-05	0.00315335	missense, intron-variant	MED16	GRCh38.p7	19:877149	ACCTCCAGCGGGTGG[C/T]CCATGGAAGGTGAGA	10025
rs745592936	snp	A/G	0.000137995	0.00830534	missense	MED16	GRCh38.p7	19:871985	CTGTCCTGGGTATCC[A/G]AGGTGGCCGTATACA	10025
rs745592992	snp	C/G	1.6708e-05	0.00289028	intron-variant	MED16	GRCh38.p7	19:873604	GGAGACGTGGGTCGG[C/G]TCAGCTCGGGCCTCT	10025
rs745623173	snp	A/C/T			intron-variant	MED16	GRCh38.p7	19:882108	ATTCCAATAAAGCCA[A/C/T]GCGGGATGGTCGCAC	10025
rs745687807	snp	C/T	1.98419e-05	0.00314969	synonymous-codon	MED16	GRCh38.p7	19:886106	GCCGCTGACCGTCAC[C/T]GCGATCCAGCCCTCC	10025
rs745692660	snp	C/T	0.00027672	0.0117594	synonymous-codon, intron-variant	MED16	GRCh38.p7	19:889767	CGCCATGCTCCAGCA[C/T]TTGATCTGCCCGTCG	10025
rs745717218	snp	A/G	3.42062e-05	0.00413545	intron-variant	MED16	GRCh38.p7	19:881728	AACTGAAAAATCAGG[A/G]GCAGGAAAACAGGAA	10025
rs745765961	snp	A/G	1.86967e-05	0.00305745	synonymous-codon	MED16	GRCh38.p7	19:868133	GATGCAGATGGTCCA[A/G]GGATCTGGGGGTCCT	10025
rs745794708	snp	A/G			intron-variant	MED16	GRCh38.p7	19:875996	CGCTTGGCACACAGC[A/G]ACGGCCCAAGGAGGG	10025
rs745809946	snp	A/G	9.85931e-05	0.00702046	synonymous-codon	MED16	GRCh38.p7	19:880009	CTTTAAGTGGACGGC[A/G]GGGCCCGCGGTGCGG	10025
rs745820328	in-del	-/CTGCCACGGGGCCCCAA	2.24772e-05	0.00335233	intron-variant	MED16	GRCh38.p7	19:876939	CCACAGGGCCCCCAC[-/CTGCCACGGGGCCCCAA]CTGCCACGGGGCCCC	10025
rs745837160	snp	C/T	1.87577e-05	0.00306243	missense	MED16	GRCh38.p7	19:871223	TCCACCAGCGCCTCG[C/T]CCGGCTCGCTCGCTG	10025
rs745890076	snp	A/G	3.95437e-05	0.00444638	intron-variant	MED16	GRCh38.p7	19:875495	CAAGGGGCCGGAGCA[A/G]AGGCGCCCGCCAAGG	10025
rs745890169	snp	A/G/T	0.000438424	0.0148	intron-variant	MED16	GRCh38.p7	19:868284	GTTAACCGCGCCGAG[A/G/T]AGAGTCCAGGGCGAG	10025
rs745908424	in-del	-/G	3.335e-05	0.00408337	frameshift-variant	MED16	GRCh38.p7	19:873551	AGCACAAATTCCTCC[-/G]GTCTTGAGGTTGATC	10025
rs745911517	snp	A/G	2.09813e-05	0.00323886	intron-variant	MED16	GRCh38.p7	19:871265	CGACCTGCGGAGAGA[A/G]GTGGCGGAAGTCTCA	10025
rs745922090	snp	A/G	1.80286e-05	0.00300233	missense, intron-variant	MED16	GRCh38.p7	19:889756	GCCAGGTGGTCCGCC[A/G]TGCTCCAGCACTTGA	10025
rs745966163	snp	C/T	3.33089e-05	0.00408085	intron-variant	MED16	GRCh38.p7	19:868356	GTAGCTGAGGAGTAG[C/T]TGAGGGGCAGCTGGG	10025
rs745998145	snp	A/G			intron-variant	MED16	GRCh38.p7	19:870150	GCCATATGCTAAGGC[A/G]TCTCTCTCCATCCAC	10025
rs746016014	snp	A/G	1.71516e-05	0.0029284	intron-variant	MED16	GRCh38.p7	19:885758	CCCACGTGATGGCCT[A/G]CGCCCGTTCACCTGC	10025
rs746029552	snp	A/G	2.27518e-05	0.00337274	intron-variant	MED16	GRCh38.p7	19:889812	GAGCCGGGAGCCTGA[A/G]GGCAAGAAGCCATCA	10025
rs746078470	snp	A/T			intron-variant	MED16	GRCh38.p7	19:869673	AAGCCGGGGGTGCCT[A/T]CCCTGGAGGTCCTGG	10025
rs746087160	snp	C/T	1.99934e-05	0.00316169	intron-variant	MED16	GRCh38.p7	19:876961	CGGGGCCCCACCTGC[C/T]ACGGGCCCCCACCTG	10025
rs746125572	snp	A/C/G/T	0.000187722	0.00968666	intron-variant	MED16	GRCh38.p7	19:873444	TAGGGGAGAGCATGG[A/C/G/T]GCACCTGGTTGGGTA	10025
rs746227968	in-del	-/CACGCCTGCA			intron-variant	MED16	GRCh38.p7	19:882386	TGTGTGGTGGTGATG[-/CACGCCTGCA]CACGCCTGCACACGC	10025
rs746243761	snp	C/T			intron-variant	MED16	GRCh38.p7	19:887526	CAAAAATTAGCCGGG[C/T]GCGGTGGTGCGTGCC	10025
rs746250239	snp	A/G			intron-variant	MED16	GRCh38.p7	19:873724	CGGGAACGAGAAGGG[A/G]GCGATGGCGTTGCCG	10025
rs746286729	snp	A/G	0.000412563	0.0143566	intron-variant	MED16	GRCh38.p7	19:881555	GCCGCTGGCTCCACC[A/G]TACCGAGGCCAGGGT	10025
rs746287943	snp	A/G	1.65803e-05	0.00287922	synonymous-codon, utr-variant-5-prime	MED16	GRCh38.p7	19:891012	GATGAGATTTCGGCA[A/G]GACCAGGCGCAGGCC	10025
rs746304471	snp	C/T	1.65619e-05	0.00287762	missense, utr-variant-5-prime	MED16	GRCh38.p7	19:891093	GACGTAGGCCAAGTC[C/T]ATCATCCCACCTGCC	10025
rs746321998	snp	C/G	2.69742e-05	0.00367238	intron-variant	MED16	GRCh38.p7	19:886207	AGGCGCCCGACTGTG[C/G]AGAAGGGAGGGAGGG	10025
rs746325955	snp	C/G			intron-variant	MED16	GRCh38.p7	19:870621	TGGGTGCCCGTGTTG[C/G]GGGTGGTTCGTGACA	10025
rs746350453	snp	A/C			intron-variant	MED16	GRCh38.p7	19:887091	TCTCAAAAACAAAAA[A/C]AAAAAGAACAAGAAA	10025
rs746386705	snp	G/T	2.00975e-05	0.00316991	intron-variant	MED16	GRCh38.p7	19:889588	TGGCGGGTGGCTGGG[G/T]AGGGTGACATCTCAT	10025
rs746409943	snp	G/T	2.58141e-05	0.00359255	missense	MED16	GRCh38.p7	19:884915	CACCCACGGGGGAGA[G/T]CTGCTGGAAGATGTT	10025
rs746425533	in-del	-/GGGGGAGAGAT			intron-variant	MED16	GRCh38.p7	19:883496	GCACGTGGGGCGGTA[-/GGGGGAGAGAT]GGGGGAGAGATGGGT	10025
rs746442060	snp	C/T	1.85057e-05	0.00304179	missense	MED16	GRCh38.p7	19:868130	CTGGATGCAGATGGT[C/T]CAGGGATCTGGGGGT	10025
rs746447561	snp	A/G/T	3.48689e-05	0.00417534	missense	MED16	GRCh38.p7	19:872103	GAAAGCTGTGGCCCG[A/G/T]CCTCAGCAGGGAACC	10025
rs746450239	in-del	-/CCTGCCCCA			intron-variant	MED16	GRCh38.p7	19:884086	GGCTTCTGAGGAGCG[-/CCTGCCCCA]CCTGCCCCACCTGCC	10025
rs746466254	in-del	-/CCCCACCTGCCACGGGG	0.00131035	0.0255628	intron-variant	MED16	GRCh38.p7	19:876933	CACCTGCCACAGGGC[-/CCCCACCTGCCACGGGG]CCCCACCTGCCACGG	10025
rs746491634	snp	C/T			intron-variant	MED16	GRCh38.p7	19:887680	CAAAAAAAATGTATT[C/T]GGTTATTTTAAAAAG	10025
rs746497509	snp	A/G	2.0285e-05	0.00318466	synonymous-codon	MED16	GRCh38.p7	19:868164	GGGAGAGTGGTGTGT[A/G]GACTGCGGGCCCAGC	10025
rs746544191	snp	C/T	2.4294e-05	0.00348517	missense	MED16	GRCh38.p7	19:884975	ACCAGCACTCCACGA[C/T]GCTGCTGGTCTGGCT	10025
rs746603108	snp	G/T	3.86361e-05	0.00439506	synonymous-codon, utr-variant-5-prime	MED16	GRCh38.p7	19:890162	CCACTCCAGGCAGGT[G/T]ATGGCCTCGTGGTGC	10025
rs746653708	snp	A/C	1.86541e-05	0.00305397	intron-variant	MED16	GRCh38.p7	19:872133	CCTGCCCGAAAGAGG[A/C]ATCGGTGTGGCTGGG	10025
rs746684957	snp	G/T	1.69913e-05	0.00291468	missense	MED16	GRCh38.p7	19:868446	CAGCGCTGCTCCCAC[G/T]GCTTCACCGCCGTGG	10025
rs746707043	snp	C/T	7.51258e-05	0.0061284	intron-variant	MED16	GRCh38.p7	19:871619	GCCTGGAAGTGGCTG[C/T]CATCCCAAAAGCACC	10025
rs746759272	snp	C/G			intron-variant	MED16	GRCh38.p7	19:883164	GGGACTTGAGGCAGG[C/G]AGAAGCTAAGCTGCT	10025
rs746759405	snp	A/C/T	3.34131e-05	0.00408725	synonymous-codon, missense	MED16	GRCh38.p7	19:873518	GAGCTGCTGCAGCGC[A/C/T]TGCAGTGTGTTCATG	10025
rs746786455	in-del	-/GTGGGGCAGGGCTAGGAAGTGGGGCAGGGCTAGGAA			intron-variant	MED16	GRCh38.p7	19:873143	GGGCAGGGCTCCGAG[lengthTooLong]GTGGGGCAGGGCTAG	10025
rs746804306	snp	C/T			intron-variant	MED16	GRCh38.p7	19:890895	TTCAAGGCAGTGGGC[C/T]GGGCACCTGGGGAAC	10025
rs746822838	in-del	-/C			upstream-variant-2KB, nc-transcript-variant	MED16, RNU6-9	GRCh38.p7	19:893542	AGAAGATTAGCATGG[-/C]CCCCTGCGCAAGGAT	10025
rs746874345	snp	A/G	7.043e-05	0.0059338	synonymous-codon	MED16	GRCh38.p7	19:885977	GGCCACCACGATGTT[A/G]CCGCCGCCGGTGAAG	10025
rs746879332	snp	A/G			intron-variant	MED16	GRCh38.p7	19:868637	CCCCACCTGCCACAG[A/G]GCCTCTGCCCATGCT	10025
rs746892774	snp	A/G	5.96843e-05	0.00546247	missense	MED16	GRCh38.p7	19:886027	CGCGGCCGCGCAGCC[A/G]GCACAGGCTCTCGGT	10025
rs746905920	in-del	-/G	8.92355e-05	0.00667906	intron-variant	MED16	GRCh38.p7	19:873414	GATGGGGGCCCAGGT[-/G]GGGGGGCGGGGCCTT	10025
rs746916013	snp	A/T	1.66729e-05	0.00288724	missense	MED16	GRCh38.p7	19:873568	TCTTGAGGTTGATCA[A/T]GACCTTGTCAATGTC	10025
rs746954572	snp	A/C	0.000218812	0.0104575	intron-variant	MED16	GRCh38.p7	19:879930	CCCACGTGCCCCAGC[A/C]GCTCACCTTCCCGTG	10025
rs746968492	in-del	-/GGGCGGGCGGGGGGGAGAGGGGAA	0.000100528	0.00708899	intron-variant	MED16	GRCh38.p7	19:871904	GCGGGGAGAGGGGAG[-/GGGCGGGCGGGGGGGAGAGGGGAA]GGGCGGGCGGGGGTG	10025
rs746984441	snp	A/G	1.70799e-05	0.00292227	intron-variant	MED16	GRCh38.p7	19:881726	CCAACTGAAAAATCA[A/G]GGGCAGGAAAACAGG	10025
rs747043861	snp	A/C/G	0.00178523	0.0298233	intron-variant	MED16	GRCh38.p7	19:886212	CCCGACTGTGGAGAA[A/C/G]GGAGGGAGGGAGGAG	10025
rs747063670	snp	C/T	1.69818e-05	0.00291387	utr-variant-5-prime	MED16	GRCh38.p7	19:891143	ACATGAGGGCAGTCA[C/T]CAGCTCCTGCGGGAG	10025
rs747073050	snp	C/G/T	3.38921e-05	0.00411645	missense	MED16	GRCh38.p7	19:872011	ATACACGGGCAGGCA[C/G/T]CTGGGCTTCAGAAGG	10025
rs747098953	snp	A/G			intron-variant	MED16	GRCh38.p7	19:885572	GGAGGAAGGCGCCCC[A/G]AACCGAGGGATTGGG	10025
rs747101051	snp	C/T	1.66944e-05	0.0028891	missense	MED16	GRCh38.p7	19:868240	GCGTCCGGCCCACGG[C/T]CTTCAACAGCCCTGC	10025
rs747128251	snp	A/C	5.58831e-05	0.00528568	missense	MED16	GRCh38.p7	19:871218	ATTCATCCACCAGCG[A/C]CTCGTCCGGCTCGCT	10025
rs747143404	snp	A/G	5.24123e-05	0.00511892	intron-variant	MED16	GRCh38.p7	19:891175	GAGGTGTGGTGGGAC[A/G]TCTATGTTGGCTGAG	10025
rs747151607	snp	A/G	1.70035e-05	0.00291572	synonymous-codon, intron-variant	MED16	GRCh38.p7	19:889695	GGACAGGGCCACAAT[A/G]GGGTCCCCCTCCACT	10025
rs747163569	snp	A/G	1.78497e-05	0.00298739	missense, intron-variant	MED16	GRCh38.p7	19:889748	AGCTATTAGCCAGGT[A/G]GTCCGCCATGCTCCA	10025
rs747164980	snp	C/T	4.34452e-05	0.00466055	synonymous-codon	MED16	GRCh38.p7	19:879970	CCCCACCAGGGCCAG[C/T]GACGTCCACGATAGC	10025
rs747216565	snp	A/G/T	9.92124e-05	0.00704258	intron-variant	MED16	GRCh38.p7	19:875489	TCACCCCAAGGGGCC[A/G/T]GAGCAGAGGCGCCCG	10025
rs747218700	snp	C/T	3.46434e-05	0.00416179	intron-variant	MED16	GRCh38.p7	19:885749	GCCTGCCAGCCCACG[C/T]GATGGCCTGCGCCCG	10025
rs747221936	snp	C/T	1.82894e-05	0.00302396	missense	MED16	GRCh38.p7	19:875433	GCGAGGCCTTCATGG[C/T]CAGGATCCGGGTGGA	10025
rs747255853	snp	C/G	8.91862e-05	0.00667721	intron-variant	MED16	GRCh38.p7	19:872895	CAGGAAGGGTGTGGC[C/G]AAGGAAAGGCTTCTT	10025
rs747303130	snp	C/T	0.000237848	0.0109026	intron-variant	MED16	GRCh38.p7	19:868280	TGAGGTTAACCGCGC[C/T]GAGGAGAGTCCAGGG	10025
rs747306922	snp	G/T	1.87019e-05	0.00305788	intron-variant	MED16	GRCh38.p7	19:871657	AGCATGGACCTGTGC[G/T]AGGAACTGGGGAAAT	10025
rs747310899	snp	A/G	7.16705e-05	0.00598582	intron-variant	MED16	GRCh38.p7	19:873405	GTCCTGATGAGATGG[A/G]GGCCCAGGTGGGGGG	10025
rs747435643	snp	C/G			intron-variant	MED16	GRCh38.p7	19:869716	GCCTTCCCCGGAGCA[C/G]GGCTGCTGGAGGTTC	10025
rs747453031	snp	C/T			intron-variant	MED16	GRCh38.p7	19:888612	ACGAAACCTCTGGAC[C/T]GTGTGGGCTGCACAC	10025
rs747481334	snp	G/T	7.02741e-05	0.00592723	intron-variant	MED16	GRCh38.p7	19:890942	CGGCCGGGAGGGGAA[G/T]CAGGTGGGAGGGGGA	10025
rs747488933	in-del	-/TTGGTGAGCGAGATGGGCAGC	1.67165e-05	0.00289102	cds-indel	MED16	GRCh38.p7	19:881605	ACCTTGAGGTCGGTG[-/TTGGTGAGCGAGATGGGCAGC]TTGGTGAGCGAGATG	10025
rs747504320	snp	A/C/G	0.000261285	0.0114273	synonymous-codon, intron-variant	MED16	GRCh38.p7	19:877163	GCCCATGGAAGGTGA[A/C/G]AGGCGGAGCACGCTC	10025
rs747542361	snp	C/G	1.78902e-05	0.00299078	intron-variant	MED16	GRCh38.p7	19:881512	CAGGGCCCAACTCCC[C/G]TGGTGTGAACTGAGG	10025
rs747559673	snp	A/G	1.79306e-05	0.00299416	missense	MED16	GRCh38.p7	19:868941	ATCTTGGGCTGGCCT[A/G]GGGCCCTGGCGGGAG	10025
rs747571227	snp	C/T	6.01534e-05	0.00548389	missense, utr-variant-5-prime	MED16	GRCh38.p7	19:886132	CCTCCATGGGCTTGC[C/T]GCCGAACAGCGTGAG	10025
rs747621025	snp	A/C	3.66032e-05	0.00427788	missense	MED16	GRCh38.p7	19:868123	CGGTCCTCTGGATGC[A/C]GATGGTCCAGGGATC	10025
rs747648738	snp	G/T	1.81404e-05	0.00301162	utr-variant-3-prime	MED16	GRCh38.p7	19:868097	CCGCCTGGACCCCCG[G/T]CCGTCACGGACGGTC	10025
rs747651578	snp	G/T	0.000101174	0.00711172	synonymous-codon, utr-variant-5-prime	MED16	GRCh38.p7	19:886193	CTCCCCGAAGCTGGA[G/T]GCGCCCGACTGTGGA	10025
rs747654923	snp	C/T			intron-variant	MED16	GRCh38.p7	19:881434	GAGCTCCTACAGCCC[C/T]ATGGCCTGTGCTCAG	10025
rs747705609	in-del	-/C			intron-variant	MED16	GRCh38.p7	19:876915	CCACCTGCCACGGGG[-/C]CCCCACCTGCCACAG	10025
rs747804406	snp	C/T	0.000299985	0.0122435	intron-variant	MED16	GRCh38.p7	19:871297	CACCCCTGACTGGGG[C/T]ACCGCCCGGCCACCC	10025
rs747864551	in-del	-/GGTGGGGTC			downstream-variant-500B	MED16	GRCh38.p7	19:867925	CAAATCGAGGTCGTG[-/GGTGGGGTC]GGTGGGGTCGGGGGC	10025
rs747883185	snp	C/T	1.73601e-05	0.00294614	missense	MED16	GRCh38.p7	19:872100	GCAGAAAGCTGTGGC[C/T]CGGCCTCAGCAGGGA	10025
rs747907401	in-del	-/GAGGGGCGGGCGGGGGGGAGAGGA	0.000432526	0.0146995	intron-variant	MED16	GRCh38.p7	19:871901	GGAGCGGGGAGAGGG[-/GAGGGGCGGGCGGGGGGGAGAGGA]GAGGGGCGGGCGGGG	10025
rs747967081	snp	A/T	1.72898e-05	0.00294017	missense	MED16	GRCh38.p7	19:868423	CACCGCACAGGCAGT[A/T]CTTGATCCAGCGCTG	10025
rs748002757	snp	G/T	0.000106028	0.00728029	intron-variant	MED16	GRCh38.p7	19:890121	CACCCCTGGCCACGT[G/T]GGACCAGCGCCTCAC	10025
rs748019398	snp	A/G	0.000130404	0.00807371	intron-variant	MED16	GRCh38.p7	19:890260	CTGTGGGGACGGGGC[A/G]TGGTCAGCACGGCCT	10025
rs748056405	snp	C/T	1.67136e-05	0.00289076	synonymous-codon	MED16	GRCh38.p7	19:873515	CAAGAGCTGCTGCAG[C/T]GCCTGCAGTGTGTTC	10025
rs748084229	snp	A/G	1.69499e-05	0.00291112	missense	MED16	GRCh38.p7	19:873456	TGGCGCACCTGGTTG[A/G]GTAGGCTGGCCAGCA	10025
rs748089616	in-del	-/AGCTGGGCTCAGGGGT	2.36672e-05	0.00343992	intron-variant	MED16	GRCh38.p7	19:868365	GAGTAGCTGAGGGGC[-/AGCTGGGCTCAGGGGT]AGCTGAGGGGCACCC	10025
rs748094812	in-del	-/AGCCCC			intron-variant	MED16	GRCh38.p7	19:878916	TTGTCAATGTCCACC[-/AGCCCC]GGCCCCGGCCCCGGC	10025
rs748113309	snp	A/C	1.73135e-05	0.00294218	missense	MED16	GRCh38.p7	19:885966	CCGTCCGCCGTGGCC[A/C]CCACGATGTTGCCGC	10025
rs748156081	snp	C/T	3.33478e-05	0.00408323	synonymous-codon	MED16	GRCh38.p7	19:871939	ACAGCAGATCCAGAG[C/T]TTGGTGAGCAGGCGG	10025
rs748158103	snp	A/G			intron-variant	MED16	GRCh38.p7	19:868554	GCGGGCCTCCCTTAC[A/G]CCTGCCCCACTTTTG	10025
rs748159188	snp	A/C	0.000101723	0.00713098	missense	MED16	GRCh38.p7	19:868490	CTTGAGCATGGTGAC[A/C]CAGCCGCACCTGCGG	10025
rs748278552	snp	A/G			intron-variant	MED16	GRCh38.p7	19:878709	GTGCCCCAGCAGCTC[A/G]CCTTCCCCTGGTTGT	10025
rs748316523	snp	A/C/T	3.38142e-05	0.00411171	utr-variant-5-prime	MED16	GRCh38.p7	19:891137	AATCACACATGAGGG[A/C/T]AGTCACCAGCTCCTG	10025
rs748334703	in-del	-/T	2.57258e-05	0.0035864	frameshift-variant	MED16	GRCh38.p7	19:879938	CCCCAGCAGCTCACC[-/T]TCCCGTGGCTGTCAA	10025
rs748338755	snp	C/T	1.68224e-05	0.00290016	missense, intron-variant	MED16	GRCh38.p7	19:889669	GCCAGTTTCACACCA[C/T]TGTGCAGCCAGGACA	10025
rs748356481	snp	C/G	0.000135953	0.00824366	missense	MED16	GRCh38.p7	19:871067	AGCTGCAGGGTGGCA[C/G]CACTGCCAGGCAGCG	10025
rs748400829	in-del	-/A	0.000151573	0.00870421	intron-variant	MED16	GRCh38.p7	19:890278	TCAGCACGGCCTGGC[-/A]ACCACAGCCTGCAGA	10025
rs748405693	snp	A/G	0.000127491	0.00798305	synonymous-codon	MED16	GRCh38.p7	19:871132	CTTGGGCTGCAGGCG[A/G]CTAACCAGGCCGTCG	10025
rs748410169	snp	C/T	9.40306e-05	0.00685613	missense	MED16	GRCh38.p7	19:868237	CAGGCGTCCGGCCCA[C/T]GGCCTTCAACAGCCC	10025
rs748459760	snp	C/T	1.96736e-05	0.00313631	intron-variant	MED16	GRCh38.p7	19:872145	AGGCATCGGTGTGGC[C/T]GGGGCGGCGGGGGGC	10025
rs748492712	in-del	-/CCCCACCTGCCACGGGC	0.000474217	0.015391	intron-variant	MED16	GRCh38.p7	19:876951	CCACCTGCCACGGGG[-/CCCCACCTGCCACGGGC]CCCCACCTGCTGCAG	10025
rs748535862	in-del	-/C			intron-variant	MED16	GRCh38.p7	19:884044	GGCCCCGGGAGCCAT[-/C]GGGGCCTCTTGACAC	10025
rs748552479	snp	A/G	9.56938e-05	0.00691648	intron-variant	MED16	GRCh38.p7	19:885031	GGAGGTGGGGGTGAG[A/G]GCTGACCCGGCACTG	10025
rs748554299	snp	C/T			intron-variant	MED16	GRCh38.p7	19:869004	GAGGCCAGGTTCCGG[C/T]AGGGGCATCTGTCCA	10025
rs748582026	snp	A/G			intron-variant	MED16	GRCh38.p7	19:881956	ATTTCATGGAAACCT[A/G]TGGGCCGGCACCATC	10025
rs748584744	snp	C/T	1.75456e-05	0.00296184	missense, intron-variant	MED16	GRCh38.p7	19:889735	ACTGAGCTCTCCCAG[C/T]TATTAGCCAGGTGGT	10025
rs748656732	snp	A/C/T	4.73062e-05	0.00486326	intron-variant	MED16	GRCh38.p7	19:880159	CAGCCCTGTGGGGCA[A/C/T]AGGCACTGCTTAGAC	10025
rs748674844	snp	A/C	0.000104915	0.007242	intron-variant	MED16	GRCh38.p7	19:885744	TCCAAGCCTGCCAGC[A/C]CACGTGATGGCCTGC	10025
rs748706474	snp	A/T	1.89788e-05	0.00308042	intron-variant	MED16	GRCh38.p7	19:871680	GGGGAAATAGCAGAT[A/T]TCAAGGCAGAGCCAC	10025
rs748732799	snp	C/T			intron-variant	MED16	GRCh38.p7	19:882652	GTGGACAGGCCACGC[C/T]ACCTCGGCTGCTAAC	10025
rs748737981	snp	A/G	1.86757e-05	0.00305573	intron-variant	MED16	GRCh38.p7	19:871653	ACAGAGCATGGACCT[A/G]TGCTAGGAACTGGGG	10025
rs748872432	snp	A/C	6.07552e-05	0.00551125	missense	MED16	GRCh38.p7	19:886055	GGTGGACGTCAGCAC[A/C]TGCCCGCTGGGCTTC	10025
rs748888768	snp	A/G	3.94283e-05	0.00443989	synonymous-codon	MED16	GRCh38.p7	19:886109	GCTGACCGTCACCGC[A/G]ATCCAGCCCTCCATG	10025
rs748892654	snp	C/T	3.34348e-05	0.00408855	intron-variant	MED16	GRCh38.p7	19:873611	TGGGTCGGGTCAGCT[C/T]GGGCCTCTTGTACAC	10025
rs748904336	snp	C/G			intron-variant	MED16	GRCh38.p7	19:877185	AGCACGCTCAGCTGC[C/G]AGAGACAGAGCCCAA	10025
rs748985687	in-del	-/AGCTGAGGAGTAGCTGAGGGGC	0.0012439	0.0249079	intron-variant	MED16	GRCh38.p7	19:868343	GGGCAGCTGAGGGGT[-/AGCTGAGGAGTAGCTGAGGGGC]AGCTGGGCTCAGGGG	10025
rs749001272	snp	A/C/T	3.38165e-05	0.00411185	missense	MED16	GRCh38.p7	19:872028	TGGGCTTCAGAAGGC[A/C/T]CCAGATGCGGATGAC	10025
rs749042739	snp	A/G	1.69186e-05	0.00290844	synonymous-codon	MED16	GRCh38.p7	19:872065	CAATTCCCGAAGCAT[A/G]CCCAGCGAGGTGCCG	10025
rs749062190	in-del	-/T			upstream-variant-2KB, nc-transcript-variant	MED16, RNU6-9	GRCh38.p7	19:893539	CAGAGAAGATTAGCA[-/T]TGGCCCCTGCGCAAG	10025
rs749085624	snp	C/T	2.97544e-05	0.00385698	missense	MED16	GRCh38.p7	19:884906	CGGGAGACTCACCCA[C/T]GGGGGAGATCTGCTG	10025
rs749156048	snp	A/C	1.97081e-05	0.00313906	missense	MED16	GRCh38.p7	19:880013	AAGTGGACGGCGGGG[A/C]CCGCGGTGCGGGGGC	10025
rs749163294	snp	A/C/T			intron-variant	MED16	GRCh38.p7	19:874824	GCGCTGAGCTGGGAC[A/C/T]GCGTCACCGTGCTGC	10025
rs749165805	snp	A/G			downstream-variant-500B	MED16	GRCh38.p7	19:867749	AAAGGCAGATGCCTG[A/G]ACAGAAGCCACCCTG	10025
rs749223673	snp	A/G	9.5495e-05	0.0069093	intron-variant	MED16	GRCh38.p7	19:868362	GAGGAGTAGCTGAGG[A/G]GCAGCTGGGCTCAGG	10025
rs749248802	snp	A/G/T	9.81019e-05	0.00700308	intron-variant	MED16	GRCh38.p7	19:876964	GGCCCCACCTGCCAC[A/G/T]GGCCCCCACCTGCTG	10025
rs749267974	snp	A/G	0.000107533	0.00733176	intron-variant	MED16	GRCh38.p7	19:890113	CGGGTCGCCACCCCT[A/G]GCCACGTGGGACCAG	10025
rs749287073	snp	A/G			synonymous-codon, utr-variant-5-prime	MED16	GRCh38.p7	19:891029	ACCAGGCGCAGGCCA[A/G]GGGCACCGATGGGCA	10025
rs749303780	snp	C/G	1.70336e-05	0.00291831	intron-variant	MED16	GRCh38.p7	19:873446	GGGGAGAGCATGGCG[C/G]ACCTGGTTGGGTAGG	10025
rs749330885	snp	A/G	1.74558e-05	0.00295425	synonymous-codon	MED16	GRCh38.p7	19:868418	GAGCCCACCGCACAG[A/G]CAGTTCTTGATCCAG	10025
rs749338217	snp	C/G			intron-variant	MED16	GRCh38.p7	19:871732	TTCTGGCGGGGGGCT[C/G]AGGCAGGACTTGTGT	10025
rs749419152	snp	C/T	1.78344e-05	0.00298611	intron-variant	MED16	GRCh38.p7	19:881528	TGGTGTGAACTGAGG[C/T]CCCGCGTGGCTGCCG	10025
rs749422186	snp	A/G	0.000150505	0.00867353	synonymous-codon	MED16	GRCh38.p7	19:885899	GATACGGCACTTCTC[A/G]CTCACCACGCTCACG	10025
rs749430649	in-del	-/T	0.000321199	0.0126687	intron-variant	MED16	GRCh38.p7	19:879898	TCCCCTGGTTGTCAA[-/T]GCCCACCAGCCCCGG	10025
rs749483673	snp	A/G	3.31203e-05	0.00406928	synonymous-codon, utr-variant-5-prime	MED16	GRCh38.p7	19:891024	GCAGGACCAGGCGCA[A/G]GCCAGGGGCACCGAT	10025
rs749501644	in-del	-/CCCCCACCTGCCACGGA	2.14296e-05	0.00327327	intron-variant	MED16	GRCh38.p7	19:876949	CCCACCTGCCACGGG[-/CCCCCACCTGCCACGGA]GCCCCACCTGCCACG	10025
rs749501861	snp	A/G	1.67329e-05	0.00289243	synonymous-codon	MED16	GRCh38.p7	19:873503	GCCCACCCACTGCAA[A/G]AGCTGCTGCAGCGCC	10025
rs749506382	snp	C/T			synonymous-codon, intron-variant	MED16	GRCh38.p7	19:877049	TACCATACTGGGCTG[C/T]ACGTGCAGCAGGATG	10025
rs749507300	snp	A/C	1.69951e-05	0.00291501	missense	MED16	GRCh38.p7	19:881564	TCCACCGTACCGAGG[A/C]CAGGGTAGAACTGTG	10025
rs749514247	snp	C/T	3.93755e-05	0.00443691	intron-variant	MED16	GRCh38.p7	19:871711	TGCCACCTGCAGGGG[C/T]TTATGTTCTGGCGGG	10025
rs749517930	in-del	-/CCCGGGGCAGGACATGGAGGGAGGGAGCCGTGTGGATTCGGGGGGT			intron-variant	MED16	GRCh38.p7	19:870793	GTGGATTCGGGGGGA[lengthTooLong]CCCGGGGCAGGACAT	10025
rs749521668	snp	A/G	3.33934e-05	0.00408603	missense	MED16	GRCh38.p7	19:881636	GGCAGCTTGGGCAGC[A/G]CCACGGCCGACACAC	10025
rs749557040	snp	A/G			intron-variant	MED16	GRCh38.p7	19:887396	AATTTGGCCGGACGC[A/G]GTGGCTCACGCCTGT	10025
rs749559665	snp	A/G	0.000133358	0.00816463	synonymous-codon	MED16	GRCh38.p7	19:875320	GTTGAGAAAGTGGGG[A/G]CGCAGCAGCGACTTC	10025
rs749568080	snp	A/G	0.000412797	0.0143606	synonymous-codon	MED16	GRCh38.p7	19:871051	CCTGGCGAGGCCGTC[A/G]AGCTGCAGGGTGGCA	10025
rs749599900	in-del	-/CCCCA					GRCh38.p7	19:879072	GCCCACCAGCCCCAG[-/CCCCA]GCCCCACGTGCCCCA	10025
rs749617620	snp	A/G			intron-variant	MED16	GRCh38.p7	19:886390	CGTCTCCTCATCTGT[A/G]AGGTGGAAGGAACGG	10025
rs749618508	snp	C/T	1.67652e-05	0.00289522	intron-variant	MED16	GRCh38.p7	19:879919	CCAGCCCCGGCCCCA[C/T]GTGCCCCAGCAGCTC	10025
rs749618820	snp	C/T			intron-variant	MED16	GRCh38.p7	19:887027	GTGATTGCAGTGAGC[C/T]GAGATCACACCATTA	10025
rs749664534	snp	A/T			intron-variant	MED16	GRCh38.p7	19:882420	TAGTCCCAGCTACTC[A/T]GGAGGCTGAGGTAGG	10025
rs749799768	snp	A/G	5.00313e-05	0.00500131	synonymous-codon	MED16	GRCh38.p7	19:875356	GGAGCTGATGGCGAT[A/G]AGGAAGAGCTTGGTG	10025
rs749823374	snp	C/T	4.26394e-05	0.00461713	intron-variant	MED16	GRCh38.p7	19:885027	CGGGGGAGGTGGGGG[C/T]GAGGGCTGACCCGGC	10025
rs749834271	snp	C/T	1.91364e-05	0.00309319	missense	MED16	GRCh38.p7	19:880086	TGTAGAAGACGGCCA[C/T]GGTCTGCAGTGAGAG	10025
rs749847162	snp	A/G			intron-variant	MED16	GRCh38.p7	19:884201	TCCCTTCTCCAGAGC[A/G]GAGGCCAGCCTAAAA	10025
rs749858499	snp	A/T	1.92639e-05	0.00310348	intron-variant	MED16	GRCh38.p7	19:872141	AAAGAGGCATCGGTG[A/T]GGCTGGGGCGGCGGG	10025
rs749860761	in-del	-/C			intron-variant	MED16	GRCh38.p7	19:873701	CAGGACACAAGGGGA[-/C]CCCACACCGGGAACG	10025
rs749877639	snp	A/T	3.34029e-05	0.00408661	intron-variant	MED16	GRCh38.p7	19:868270	CAGGGCGGGCTGAGG[A/T]TAACCGCGCCGAGGA	10025
rs749913344	snp	A/C	2.76476e-05	0.00371793	intron-variant	MED16	GRCh38.p7	19:875479	GGAAGCCAGGTCACC[A/C]CAAGGGGCCGGAGCA	10025
rs749981319	snp	C/T	0.000282611	0.0118838	intron-variant	MED16	GRCh38.p7	19:885736	TGCTTCATTCCAAGC[C/T]TGCCAGCCCACGTGA	10025
rs749983377	snp	A/G	0.000157094	0.00886128	missense, intron-variant	MED16	GRCh38.p7	19:889783	TTGATCTGCCCGTCG[A/G]CATCTGCTGACAGGA	10025
rs750070837	snp	A/G			intron-variant	MED16	GRCh38.p7	19:890847	CAGAGGAGGGCCAGG[A/G]TGAGTGAGAGGTGGC	10025
rs750077734	snp	C/G			intron-variant	MED16	GRCh38.p7	19:891284	GGCCCGGAGGCCAGA[C/G]AGAGCCTGGGGCTGG	10025
rs750079791	snp	A/G	1.7383e-05	0.00294808	intron-variant	MED16	GRCh38.p7	19:873425	CAGGTGGGGGGCGGG[A/G]CCTTAGGGGAGAGCA	10025
rs750126553	snp	A/G/T	9.58267e-05	0.00692129	missense	MED16	GRCh38.p7	19:868942	TCTTGGGCTGGCCTG[A/G/T]GGCCCTGGCGGGAGA	10025
rs750127474	snp	C/T	1.79245e-05	0.00299365	intron-variant	MED16	GRCh38.p7	19:890930	CGGGACACCATGCGG[C/T]CGGGAGGGGAAGCAG	10025
rs750142946	snp	C/T	2.42662e-05	0.00348318	missense, intron-variant	MED16	GRCh38.p7	19:877176	GAGAGGCGGAGCACG[C/T]TCAGCTGCCAGAGAC	10025
rs750155129	in-del	-/GCCCCGCGCCCCGCGCCCCGC			intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:892882	AACCCTGAGCCCCGA[-/GCCCCGCGCCCCGCGCCCCGC]GCCCCGCGCCCCGCG	10025
rs750255876	in-del	-/GCCGCGCA	1.93934e-05	0.00311389	frameshift-variant	MED16	GRCh38.p7	19:886016	GGCCAGGGCCACGCG[-/GCCGCGCA]GCCGGCACAGGCTCT	10025
rs750276445	snp	C/T			intron-variant	MED16	GRCh38.p7	19:887405	GGACGCGGTGGCTCA[C/T]GCCTGTAATCTCAGC	10025
rs750287076	snp	A/G	5.02845e-05	0.00501395	synonymous-codon, utr-variant-5-prime	MED16	GRCh38.p7	19:890973	CGCACCCTGGTCATC[A/G]CTGCGCAGGTCCATG	10025
rs750329096	snp	A/C	3.00413e-05	0.00387553	intron-variant	MED16	GRCh38.p7	19:886223	AGAAGGGAGGGAGGG[A/C]GGAGGGGCCGCTCAG	10025
rs750358097	in-del	-/CAGCGC	5.39617e-05	0.00519403	cds-indel, intron-variant	MED16	GRCh38.p7	19:877120	GAAGAGCAGGTGCCG[-/CAGCGC]CAGCGCCAGCCCCAC	10025
rs750429963	snp	A/G	1.69017e-05	0.00290699	missense	MED16	GRCh38.p7	19:872058	CCACCATCAATTCCC[A/G]AAGCATGCCCAGCGA	10025
rs750430172	snp	C/T	1.67508e-05	0.00289398	missense	MED16	GRCh38.p7	19:875279	CAGATCTCGGTCAGC[C/T]GGTCGCCGGGGCTCT	10025
rs750450297	snp	G/T			upstream-variant-2KB, downstream-variant-500B	MED16, RNU6-9	GRCh38.p7	19:893913	CTTCCATTTTCTAAT[G/T]TCCAAGAGTGGGGAA	10025
rs750459174	snp	A/G			intron-variant	MED16	GRCh38.p7	19:870476	TGAGGTAGGAGAATC[A/G]TTTGAACCCGAGAGG	10025
rs750472253	snp	A/G	1.91532e-05	0.00309455	synonymous-codon	MED16	GRCh38.p7	19:868149	GGATCTGGGGGTCCT[A/G]GGAGAGTGGTGTGTG	10025
rs750646530	snp	C/G			intron-variant	MED16	GRCh38.p7	19:889188	CTATCTTAACTGTCC[C/G]CCCCAACCCTGGCCA	10025
rs750648834	snp	C/G			intron-variant	MED16	GRCh38.p7	19:881333	TCTTTACATATTAAA[C/G]AACACTGGATCTGTC	10025
rs750668906	snp	C/T	1.80351e-05	0.00300287	intron-variant	MED16	GRCh38.p7	19:868407	ACCCGCCACCAGAGC[C/T]CACCGCACAGGCAGT	10025
rs750723183	snp	A/G	3.76088e-05	0.00433624	intron-variant	MED16	GRCh38.p7	19:871609	GCAAACAGGTGCCTG[A/G]AAGTGGCTGCCATCC	10025
rs750760424	snp	C/T	1.67888e-05	0.00289726	missense	MED16	GRCh38.p7	19:873487	GGTACAGCACGAAGT[C/T]GCCCACCCACTGCAA	10025
rs750771352	snp	C/T			intron-variant	MED16	GRCh38.p7	19:888242	AAGATAAAGGTCTGG[C/T]CGGGCTCGTTGGCTC	10025
rs750776744	snp	A/G	1.68741e-05	0.00290461	missense	MED16	GRCh38.p7	19:868470	GCCGTGGTTCTGTTG[A/G]GCGACTTGAGCATGG	10025
rs750823085	snp	C/T			downstream-variant-500B	MED16	GRCh38.p7	19:867590	GCAGCTGGAGAAACA[C/T]AACAGGGACAGAGTC	10025
rs750832060	in-del	-/ACGGCCTTCAACAGCCCTGCAGG	0.000401762	0.0141675	intron-variant	MED16	GRCh38.p7	19:868236	GCAGGCGTCCGGCCC[-/ACGGCCTTCAACAGCCCTGCAGG]GCGGGCTGAGGTTAA	10025
rs750947718	snp	A/T	8.36967e-05	0.00646849	missense, utr-variant-5-prime	MED16	GRCh38.p7	19:891122	CCGCTGGCCGCCGCA[A/T]ATCACACATGAGGGC	10025
rs750975572	snp	A/G			intron-variant	MED16	GRCh38.p7	19:875197	AATAAAAATAAAATA[A/G]ATAGATGAAAGAAAC	10025
rs750985147	in-del	-/GGGCCCCCACCTGCCACGGGGCCCCACCTGCCAC			intron-variant	MED16	GRCh38.p7	19:876930	CCCCCACCTGCCACA[lengthTooLong]GGGCCCCCACCTGCT	10025
rs751092708	snp	A/G	5.53725e-05	0.00526148	missense	MED16	GRCh38.p7	19:871121	CGAAGGGGCTGCTTG[A/G]GCTGCAGGCGGCTAA	10025
rs751113892	snp	C/T	1.7119e-05	0.00292562	synonymous-codon, intron-variant	MED16	GRCh38.p7	19:889638	GGGCAGGACACTCAC[C/T]TTCTCCACGTGCAGG	10025
rs751147997	snp	A/G	3.94851e-05	0.00444308	synonymous-codon	MED16	GRCh38.p7	19:871167	CTGGCAGCCAGTCCA[A/G]GCTGGGGATAAGCAG	10025
rs751153421	snp	A/G			intron-variant	MED16	GRCh38.p7	19:874567	TACGGCAAAACGGAA[A/G]GAGGAGCAGACCTGC	10025
rs751178329	snp	A/G	5.34174e-05	0.00516777	intron-variant	MED16	GRCh38.p7	19:885720	GGACCCTGAGAAGCA[A/G]TGCTTCATTCCAAGC	10025
rs751194403	in-del	-/C	1.79696e-05	0.00299741	frameshift-variant, intron-variant	MED16	GRCh38.p7	19:876984	CCACCTGCTGCAGGG[-/C]CAGCGGTCTGGCGCG	10025
rs751203748	snp	C/T	1.71443e-05	0.00292777	missense, intron-variant	MED16	GRCh38.p7	19:889705	ACAATGGGGTCCCCC[C/T]CCACTAGGCTGCCCA	10025
rs751223812	snp	C/T			upstream-variant-2KB, downstream-variant-500B	MED16, RNU6-9	GRCh38.p7	19:893640	TCTTGCTCTGTTGCC[C/T]AGGCTGGAATGCAAT	10025
rs751225819	snp	C/T			intron-variant	MED16	GRCh38.p7	19:884524	TGCACCGCCCCTGCC[C/T]GGTCTGGCCTGTCCC	10025
rs751236372	snp	A/C			stop-gained	MED16	GRCh38.p7	19:872055	TGACCACCATCAATT[A/C]CCGAAGCATGCCCAG	10025
rs751254645	snp	A/C/G	6.31125e-05	0.0056172	intron-variant	MED16	GRCh38.p7	19:872158	GCTGGGGCGGCGGGG[A/C/G]GCAGATGGCGATGGG	10025
rs751265880	snp	A/G	8.62292e-05	0.0065656	synonymous-codon	MED16	GRCh38.p7	19:880140	CGTCGTGGAAGGCCA[A/G]GGCCAGCCCTGTGGG	10025
rs751319315	snp	A/C	3.43242e-05	0.00414257	intron-variant	MED16	GRCh38.p7	19:868531	ACTGAGCGGGTTCCC[A/C]CTTCCAGGCGGGCCT	10025
rs751343498	snp	A/C			intron-variant	MED16	GRCh38.p7	19:869257	GCCACGTGCCCGGGG[A/C]GCCTGAGGTGCAGGG	10025
rs751346651	snp	A/G			intron-variant	MED16	GRCh38.p7	19:870060	TCCAGAGAAAGGCCA[A/G]CCCCGGGCCCTGCAA	10025
rs751397751	snp	A/G			intron-variant	MED16	GRCh38.p7	19:869354	TCTGCCCAGACACCC[A/G]GCCTGGAGGTGCCGG	10025
rs751398178	snp	A/G			intron-variant	MED16	GRCh38.p7	19:881141	ACTTGTCCACATTTT[A/G]CAGCTGAGCAAATAG	10025
rs751410719	in-del	-/CCCCACCTGCCACGGGG	0.00131035	0.0255628	intron-variant	MED16	GRCh38.p7	19:876934	CACCTGCCACAGGGC[-/CCCCACCTGCCACGGGG]CCCCACCTGCCACGG	10025
rs751482017	snp	A/G/T	7.04207e-05	0.00593349	intron-variant	MED16	GRCh38.p7	19:880191	TGGGCAGGGCCCAGG[A/G/T]CACGCCCGCCGGGGG	10025
rs751511690	snp	A/G	0.000134728	0.00820645	missense, intron-variant	MED16	GRCh38.p7	19:877143	AGCCCCACCTCCAGC[A/G]GGTGGCCCATGGAAG	10025
rs751532961	snp	C/T	1.98758e-05	0.00315238	synonymous-codon	MED16	GRCh38.p7	19:886100	GACCAGGCCGCTGAC[C/T]GTCACCGCGATCCAG	10025
rs751574554	snp	C/G	2.00616e-05	0.00316708	intron-variant	MED16	GRCh38.p7	19:868835	AGCGGCACATCTCTG[C/G]GAGTCAGCGGTTCCG	10025
rs751604368	snp	A/C/T	4.8105e-05	0.00490414	missense, intron-variant	MED16	GRCh38.p7	19:877174	GTGAGAGGCGGAGCA[A/C/T]GCTCAGCTGCCAGAG	10025
rs751605728	snp	A/G	6.75699e-05	0.00581209	synonymous-codon	MED16	GRCh38.p7	19:872052	GGATGACCACCATCA[A/G]TTCCCGAAGCATGCC	10025
rs751649566	snp	C/T	1.76176e-05	0.00296791	intron-variant	MED16	GRCh38.p7	19:875223	GAAACCTCGAGGCCC[C/T]GGGCGTGGAAAAGGA	10025
rs751688609	snp	C/T	6.74468e-05	0.00580679	intron-variant	MED16	GRCh38.p7	19:884854	CAAAATAAAAACCAA[C/T]CGCCCCCGAGGGCAG	10025
rs751728446	snp	A/G	1.98285e-05	0.00314863	missense	MED16	GRCh38.p7	19:880007	GCCTTTAAGTGGACG[A/G]CGGGGCCCGCGGTGC	10025
rs751731056	snp	C/T	0.000166875	0.0091329	intron-variant	MED16	GRCh38.p7	19:871257	CCTCATCGCGACCTG[C/T]GGAGAGAGGTGGCGG	10025
rs751752906	snp	A/G			intron-variant	MED16	GRCh38.p7	19:882515	GGCAACACAGCAAGA[A/G]CCTAGCTCAAAAACA	10025
rs751794796	snp	C/G	1.94899e-05	0.00312163	missense	MED16	GRCh38.p7	19:880028	CCCGCGGTGCGGGGG[C/G]GCTTCATGGCCGGCT	10025
rs751800037	snp	A/G/T	0.000171424	0.00925648	intron-variant	MED16	GRCh38.p7	19:871259	TCATCGCGACCTGCG[A/G/T]AGAGAGGTGGCGGAA	10025
rs751855206	snp	A/G	4.38395e-05	0.00468165	missense, intron-variant	MED16	GRCh38.p7	19:889802	CTGCTGACAGGAGCC[A/G]GGAGCCTGAGGGCAA	10025
rs751875362	snp	C/T	5.10061e-05	0.0050498	synonymous-codon	MED16	GRCh38.p7	19:872086	CGAGGTGCCGTCCCG[C/T]AGAAAGCTGTGGCCC	10025
rs751880674	snp	A/C	3.8387e-05	0.00438087	missense	MED16	GRCh38.p7	19:880062	CCACAGGCCTCGGGG[A/C]CGCGGAGCTGTAGAA	10025
rs751883484	snp	C/T			intron-variant	MED16	GRCh38.p7	19:881849	CGCCCTGCTCCCATG[C/T]CCAGAAGACCAGGCC	10025
rs751901503	snp	C/G	2.36756e-05	0.00344053	intron-variant	MED16	GRCh38.p7	19:868345	GCAGCTGAGGGGTAG[C/G]TGAGGAGTAGCTGAG	10025
rs751934483	snp	C/T	0.000155618	0.00881956	intron-variant	MED16	GRCh38.p7	19:871579	CACATACACACAACC[C/T]GACAAGGAGAGACAG	10025
rs751954533	snp	A/G	1.87612e-05	0.00306272	intron-variant	MED16	GRCh38.p7	19:868399	TGAGGGGCACCCGCC[A/G]CCAGAGCCCACCGCA	10025
rs751983882	snp	C/T			intron-variant	MED16	GRCh38.p7	19:888583	GTGGTGGCCGCACAA[C/T]ATGGCGAGTGTATAC	10025
rs751988431	snp	C/T	5.33604e-05	0.00516501	missense, intron-variant	MED16	GRCh38.p7	19:876988	CCTGCTGCAGGGCAG[C/T]GGTCTGGCGCGTGTA	10025
rs752000848	snp	A/C/G	3.33263e-05	0.00408194	missense, synonymous-codon	MED16	GRCh38.p7	19:885871	TGAACAGGGAGGGCA[A/C/G]GATCTCCGTGTCGAT	10025
rs752004209	snp	C/G			intron-variant	MED16	GRCh38.p7	19:868319	GGCTCTTGCAGCAGC[C/G]GGGCTCAGGGGCAGC	10025
rs752013583	snp	C/T	1.73006e-05	0.00294109	intron-variant	MED16	GRCh38.p7	19:881550	TGGCTGCCGCTGGCT[C/T]CACCGTACCGAGGCC	10025
rs752047775	snp	G/T	1.68391e-05	0.0029016	missense	MED16	GRCh38.p7	19:873474	AGGCTGGCCAGCAGG[G/T]ACAGCACGAAGTCGC	10025
rs752115843	snp	A/G	1.69235e-05	0.00290886	missense	MED16	GRCh38.p7	19:885939	TAGAACTGCACGGGC[A/G]ACGCGCTGCTGCCGT	10025
rs752130392	in-del	-/TAGGAACTGG	1.8704e-05	0.00305805	intron-variant	MED16	GRCh38.p7	19:871656	AGCATGGACCTGTGC[-/TAGGAACTGG]TAGGAACTGGGGAAA	10025
rs752149668	snp	A/G	3.90533e-05	0.00441873	intron-variant	MED16	GRCh38.p7	19:871707	CCACTGCCACCTGCA[A/G]GGGCTTATGTTCTGG	10025
rs752155305	snp	C/G	1.68193e-05	0.00289989	intron-variant	MED16	GRCh38.p7	19:877220	AGCCCGGTGAGATGG[C/G]GCTGCGCCCTCAGCC	10025
rs752203696	snp	A/G	1.67069e-05	0.00289019	missense	MED16	GRCh38.p7	19:881613	GGTCGGTGTTGGTGA[A/G]CGAGATGGGCAGCTT	10025
rs752207000	snp	G/T	7.60803e-05	0.0061672	intron-variant	MED16	GRCh38.p7	19:871919	GGGGCGGGCGGGGGT[G/T]CCTCACAGCAGATCC	10025
rs752262164	snp	G/T	0.000377715	0.0137373	intron-variant	MED16	GRCh38.p7	19:871005	GGAGGAAGGAGTCCT[G/T]TGTTTGGGGACCAAT	10025
rs752300643	snp	A/G			intron-variant	MED16	GRCh38.p7	19:875877	TGAAGCATTTTGGGA[A/G]GCTGAGGCTGGAGGA	10025
rs752316545	snp	A/C/T	6.03155e-05	0.00549127	intron-variant	MED16	GRCh38.p7	19:879908	GTCAATGCCCACCAG[A/C/T]CCCGGCCCCACGTGC	10025
rs752325815	snp	G/T	3.46981e-05	0.00416508	intron-variant	MED16	GRCh38.p7	19:889629	CGCTCACTCGGGCAG[G/T]ACACTCACCTTCTCC	10025
rs752336807	snp	A/G	0.000108776	0.00737403	intron-variant	MED16	GRCh38.p7	19:886243	GGGCCGCTCAGGCTC[A/G]TGGGGGCTGCCCCAT	10025
rs752393248	snp	C/G	1.84269e-05	0.00303531	intron-variant	MED16	GRCh38.p7	19:872129	GAACCCTGCCCGAAA[C/G]AGGCATCGGTGTGGC	10025
rs752396215	snp	A/G	1.66704e-05	0.00288703	synonymous-codon	MED16	GRCh38.p7	19:875344	CGACTTCAGGGTGGA[A/G]CTGATGGCGATGAGG	10025
rs752405881	snp	C/T	0.000175768	0.00937299	missense	MED16	GRCh38.p7	19:868220	AAGCTCTGCTGGTCA[C/T]GCAGGCGTCCGGCCC	10025
rs752407418	in-del	-/G	0.0046252	0.0478665	intron-variant	MED16	GRCh38.p7	19:872961	GGGGGAGGGCTCCGA[-/G]GGTGGGGCAGGGCTC	10025
rs752429814	snp	C/T	4.70455e-05	0.0048498	missense	MED16	GRCh38.p7	19:884969	GCAGGGACCAGCACT[C/T]CACGATGCTGCTGGT	10025
rs752444603	snp	A/G	5.61256e-05	0.00529714	intron-variant	MED16	GRCh38.p7	19:871615	AGGTGCCTGGAAGTG[A/G]CTGCCATCCCAAAAG	10025
rs752448968	snp	A/G	1.96153e-05	0.00313166	synonymous-codon	MED16	GRCh38.p7	19:868158	GGTCCTGGGAGAGTG[A/G]TGTGTGGACTGCGGG	10025
rs752460156	snp	A/G	0.000406091	0.0142436	missense	MED16	GRCh38.p7	19:871107	GGCCAAACTGCAGAC[A/G]AAGGGGCTGCTTGGG	10025
rs752475500	snp	A/G			upstream-variant-2KB	MED16	GRCh38.p7	19:894431	CCACCCCGGCCTCCC[A/G]AAGTGCTGGGATTAT	10025
rs752497781	snp	C/G			upstream-variant-2KB, downstream-variant-500B	MED16, RNU6-9	GRCh38.p7	19:893786	TATTTTGGTAGAGAC[C/G]GGGTTTCGCCATGTT	10025
rs752549057	snp	C/G	2.07773e-05	0.00322307	intron-variant	MED16	GRCh38.p7	19:872155	GTGGCTGGGGCGGCG[C/G]GGGGCAGATGGCGAT	10025
rs752681089	snp	A/G	1.94566e-05	0.00311896	missense	MED16	GRCh38.p7	19:880107	GCAGTGAGAGCCGGT[A/G]CACGATGTGGACGCT	10025
rs752681351	snp	C/T	1.87566e-05	0.00306235	missense, intron-variant	MED16	GRCh38.p7	19:877137	AGCGCCAGCCCCACC[C/T]CCAGCGGGTGGCCCA	10025
rs752695595	snp	A/G	4.19076e-05	0.00457734	synonymous-codon	MED16	GRCh38.p7	19:880132	GACGCTGCCGTCGTG[A/G]AAGGCCAGGGCCAGC	10025
rs752696230	snp	A/G	1.69916e-05	0.00291471	synonymous-codon, intron-variant	MED16	GRCh38.p7	19:877060	GCTGCACGTGCAGCA[A/G]GATGTCCCACCAGTC	10025
rs752718389	snp	C/T			upstream-variant-2KB, nc-transcript-variant	MED16, RNU6-9	GRCh38.p7	19:893491	CAATATTCGTGCTCG[C/T]TTCGGCAGCACATAT	10025
rs752726785	in-del	-/AAG			intron-variant	MED16	GRCh38.p7	19:887095	AAAAACAAAAAAAAA[-/AAG]AACAAGAAAAATGTC	10025
rs752749561	snp	A/C/T	3.72393e-05	0.00431492	intron-variant	MED16	GRCh38.p7	19:871644	AGCACCCACACAGAG[A/C/T]ATGGACCTGTGCTAG	10025
rs752763676	snp	A/G			intron-variant	MED16	GRCh38.p7	19:887439	TTGGGAGGCCGAGGC[A/G]GGCAGATCTCAAGGT	10025
rs752786002	snp	A/G			intron-variant	MED16	GRCh38.p7	19:886771	CCTTCTTTCAACGTG[A/G]GTCTTTTAAAAGATG	10025
rs752808867	in-del	-/C			intron-variant	MED16	GRCh38.p7	19:881849	CGCCCTGCTCCCATG[-/C]CCAGAAGACCAGGCC	10025
rs752815456	snp	A/G	8.99256e-05	0.00670483	intron-variant	MED16	GRCh38.p7	19:890924	ACAGGGCGGGACACC[A/G]TGCGGCCGGGAGGGG	10025
rs752815493	snp	A/G	1.97467e-05	0.00314212	synonymous-codon	MED16	GRCh38.p7	19:886019	CAGGGCCACGCGGCC[A/G]CGCAGCCGGCACAGG	10025
rs752837641	snp	C/G			upstream-variant-2KB	MED16	GRCh38.p7	19:894748	TGGGAAACATAGCCA[C/G]ACCCCGTCTCTACAA	10025
rs752847260	snp	C/G	0.000183629	0.00958022	intron-variant	MED16	GRCh38.p7	19:873597	TCTACAAGGAGACGT[C/G]GGTCGGGTCAGCTCG	10025
rs752851484	snp	A/G	1.69493e-05	0.00291108	missense	MED16	GRCh38.p7	19:881714	GGCTGTTTGTCGCCA[A/G]CTGAAAAATCAGGGG	10025
rs752859155	snp	A/C/T	0.00020266	0.0100646	intron-variant	MED16	GRCh38.p7	19:868822	CTGAGCCATCCCCAG[A/C/T]GGCACATCTCTGGGA	10025
rs752905296	snp	C/T	0.000179446	0.00947051	missense	MED16	GRCh38.p7	19:886093	ACACGGTGACCAGGC[C/T]GCTGACCGTCACCGC	10025
rs752991821	snp	A/G	5.19809e-05	0.00509782	intron-variant	MED16	GRCh38.p7	19:891165	CTGCGGGAGGGAGGT[A/G]TGGTGGGACGTCTAT	10025
rs753009632	snp	A/G	1.68975e-05	0.00290662	missense	MED16	GRCh38.p7	19:872042	CCCCAGATGCGGATG[A/G]CCACCATCAATTCCC	10025
rs753015504	snp	A/G			synonymous-codon	MED16	GRCh38.p7	19:871072	CAGGGTGGCAGCACT[A/G]CCAGGCAGCGTGGGC	10025
rs753048211	snp	A/G			intron-variant	MED16	GRCh38.p7	19:871341	AGCCCCTCCAGTTCA[A/G]GAGCACCAGGTCAGG	10025
rs753058407	snp	C/T	0.000516221	0.0160575	missense	MED16	GRCh38.p7	19:880005	TAGCCTTTAAGTGGA[C/T]GGCGGGGCCCGCGGT	10025
rs753109618	in-del	-/GAGA	1.92658e-05	0.00310363	intron-variant	MED16	GRCh38.p7	19:871586	ACACAACCCGACAAG[-/GAGA]GACAGCAAACAGGTG	10025
rs753116958	snp	A/G	1.94873e-05	0.00312142	missense	MED16	GRCh38.p7	19:880025	GGGCCCGCGGTGCGG[A/G]GGCGCTTCATGGCCG	10025
rs753131046	snp	A/G	2.1158e-05	0.00325247	synonymous-codon, intron-variant	MED16	GRCh38.p7	19:889797	GGCATCTGCTGACAG[A/G]AGCCGGGAGCCTGAG	10025
rs753147556	snp	A/G	3.33795e-05	0.00408517	synonymous-codon	MED16	GRCh38.p7	19:885803	GGCCAGGAACTTGAG[A/G]TGGGTGATGGCGGGA	10025
rs753169278	snp	C/T			intron-variant	MED16	GRCh38.p7	19:890329	AGGCTCCAGGTAAGC[C/T]GGTGTGTGTCCCACC	10025
rs753197657	in-del	-/AGCTGAGGGGT/AGCTGAGGGGTAGCTGAGGAGT	7.63631e-05	0.00617865	intron-variant	MED16	GRCh38.p7	19:868331	GCCGGGCTCAGGGGC[lengthTooLong]AGCTGAGGGGTAGCT	10025
rs753225502	snp	A/G			intron-variant	MED16	GRCh38.p7	19:890715	CCTCCGTCAACCAAC[A/G]CTCCAGCCCGATTCG	10025
rs753278863	snp	C/G	3.30535e-05	0.00406518	intron-variant	MED16	GRCh38.p7	19:889848	AACCTTCCAGGGATG[C/G]GCAGAGCACTGCGTT	10025
rs753304311	snp	C/T	6.94477e-05	0.00589228	intron-variant	MED16	GRCh38.p7	19:876946	GGCCCCCACCTGCCA[C/T]GGGGCCCCACCTGCC	10025
rs753349779	snp	A/G			intron-variant	MED16	GRCh38.p7	19:871466	CTCTCCCCGTCTCTG[A/G]CCTGTCATGAGACTC	10025
rs753362598	snp	C/G	1.96489e-05	0.00313433	intron-variant	MED16	GRCh38.p7	19:868393	GGTAGCTGAGGGGCA[C/G]CCGCCACCAGAGCCC	10025
rs753371301	snp	C/G			intron-variant	MED16	GRCh38.p7	19:888306	GCAGACGGATCACCT[C/G]AGGTGAGAAGTTCGA	10025
rs753438629	snp	C/T	1.66416e-05	0.00288453	missense	MED16	GRCh38.p7	19:885856	CGGTGGTGCAGCGCA[C/T]GAACAGGGAGGGCAG	10025
rs753464658	snp	C/T	1.65411e-05	0.00287581	missense, utr-variant-5-prime	MED16	GRCh38.p7	19:891076	CATTTCTCCCACTCA[C/T]AGACGTAGGCCAAGT	10025
rs753481390	snp	A/G			intron-variant	MED16	GRCh38.p7	19:886786	AGTCTTTTAAAAGAT[A/G]GGGTCTTGGCTGCGC	10025
rs753485798	snp	C/T	1.66507e-05	0.00288532	missense, utr-variant-5-prime	MED16	GRCh38.p7	19:890985	ATCGCTGCGCAGGTC[C/T]ATGGTGAAGGCGATG	10025
rs753488360	snp	C/T	3.47681e-05	0.00416927	intron-variant	MED16	GRCh38.p7	19:881545	CCGCGTGGCTGCCGC[C/T]GGCTCCACCGTACCG	10025
rs753548678	snp	A/G			intron-variant	MED16	GRCh38.p7	19:876419	ACCACAGGGCCACCG[A/G]GTGTGCATCCTGGTA	10025
rs753550272	snp	C/T	5.32269e-05	0.00515855	intron-variant	MED16	GRCh38.p7	19:870989	TCCCGGGGCAGGACA[C/T]GGAGGAAGGAGTCCT	10025
rs753703015	snp	A/T	1.72175e-05	0.00293402	missense	MED16	GRCh38.p7	19:872094	CGTCCCGCAGAAAGC[A/T]GTGGCCCGGCCTCAG	10025
rs753727687	in-del	-/A	3.03361e-05	0.0038945	intron-variant	MED16	GRCh38.p7	19:886226	AGGGAGGGAGGGAGG[-/A]GGGGCCGCTCAGGCT	10025
rs753743095	in-del	-/GAC			intron-variant	MED16	GRCh38.p7	19:872366	AGTCCACAAGACTAA[-/GAC]GAGGCTCTGGCTGAG	10025
rs753799025	snp	A/G	1.66699e-05	0.00288698	synonymous-codon	MED16	GRCh38.p7	19:875338	CAGCAGCGACTTCAG[A/G]GTGGAGCTGATGGCG	10025
rs753850248	snp	A/C/G	5.46994e-05	0.00522946	intron-variant	MED16	GRCh38.p7	19:872125	CAGGGAACCCTGCCC[A/C/G]AAAGAGGCATCGGTG	10025
rs753870356	snp	G/T	1.72133e-05	0.00293366	missense, intron-variant	MED16	GRCh38.p7	19:877005	GTCTGGCGCGTGTAC[G/T]CCTCGTGCAGCTTCT	10025
rs753901442	snp	A/G			intron-variant	MED16	GRCh38.p7	19:881196	CTCACTCATGGGCAC[A/G]GATGCCACGGTTTGA	10025
rs753901870	snp	A/G	2.17706e-05	0.00329922	intron-variant	MED16	GRCh38.p7	19:890255	CAGGTCTGTGGGGAC[A/G]GGGCATGGTCAGCAC	10025
rs753920641	snp	G/T	1.87366e-05	0.00306071	intron-variant	MED16	GRCh38.p7	19:871613	ACAGGTGCCTGGAAG[G/T]GGCTGCCATCCCAAA	10025
rs753921287	snp	A/C			intron-variant	MED16	GRCh38.p7	19:890729	CGCTCCAGCCCGATT[A/C]GATCCCGCACACGGG	10025
rs753980174	snp	G/T	0.000101928	0.00713818	missense, intron-variant	MED16	GRCh38.p7	19:877042	GGCTCTGTACCATAC[G/T]GGGCTGCACGTGCAG	10025
rs753989886	snp	A/G	6.888e-05	0.00586816	missense	MED16	GRCh38.p7	19:885957	GCGCTGCTGCCGTCC[A/G]CCGTGGCCACCACGA	10025
rs754076148	snp	C/T	0.000103488	0.00719257	intron-variant	MED16	GRCh38.p7	19:890338	GTAAGCCGGTGTGTG[C/T]CCCACCCCAGGAAGG	10025
rs754079148	snp	C/T			intron-variant	MED16	GRCh38.p7	19:887466	AGGTCAGGAGTTCGA[C/T]ACCATCCTGGCCAAG	10025
rs754094568	snp	A/G	0.00011581	0.00760865	synonymous-codon	MED16	GRCh38.p7	19:886013	GTCGGCCAGGGCCAC[A/G]CGGCCGCGCAGCCGG	10025
rs754108976	in-del	-/AG			intron-variant	MED16	GRCh38.p7	19:868326	GCAGCAGCCGGGCTC[-/AG]GGGCAGCTGAGGGGT	10025
rs754141176	snp	A/G			intron-variant	MED16	GRCh38.p7	19:874415	ACGCCCAGCAACCCT[A/G]ATTTTTAAAAGAAAC	10025
rs754159368	snp	C/G	1.66918e-05	0.00288888	intron-variant	MED16	GRCh38.p7	19:873594	ATGTCTACAAGGAGA[C/G]GTGGGTCGGGTCAGC	10025
rs754171521	snp	A/G			upstream-variant-2KB	MED16	GRCh38.p7	19:894463	GGCGTGAGCCACCGC[A/G]GCCTCACTGCATGAT	10025
rs754203709	snp	A/T	1.67728e-05	0.00289588	synonymous-codon	MED16	GRCh38.p7	19:881692	GATCCGCCATTTGAG[A/T]ATTGTGGGCTGTTTG	10025
rs754241655	snp	G/T	2.61537e-05	0.0036161	missense	MED16	GRCh38.p7	19:871128	GCTGCTTGGGCTGCA[G/T]GCGGCTAACCAGGCC	10025
rs754244204	snp	A/G	1.72204e-05	0.00293427	intron-variant	MED16	GRCh38.p7	19:891160	AGCTCCTGCGGGAGG[A/G]AGGTGTGGTGGGACG	10025
rs754266554	snp	A/G/T	3.46616e-05	0.00416291	intron-variant	MED16	GRCh38.p7	19:881748	GAAAACAGGAAGGCA[A/G/T]TGGAGTAAAGACAGG	10025
rs754300737	snp	C/G/T	0.000101056	0.00710771	missense, utr-variant-5-prime	MED16	GRCh38.p7	19:891131	GCCGCAAATCACACA[C/G/T]GAGGGCAGTCACCAG	10025
rs754354623	snp	A/G	5.08419e-05	0.00504166	missense	MED16	GRCh38.p7	19:875405	GTCACCGTGCAGGGC[A/G]ACAGCTTGCAGAGCG	10025
rs754450994	snp	A/G	1.97892e-05	0.00314551	missense	MED16	GRCh38.p7	19:880002	GCATAGCCTTTAAGT[A/G]GACGGCGGGGCCCGC	10025
rs754454296	snp	G/T			intron-variant	MED16	GRCh38.p7	19:871535	TTTTCCAGACACTGG[G/T]ATGTAAGAATGACAC	10025
rs754462464	snp	A/G/T	0.000130316	0.00807114	utr-variant-3-prime	MED16	GRCh38.p7	19:868062	ACCGAGGAGACGCCC[A/G/T]AGCCGGGTCACCACA	10025
rs754544271	snp	A/G	1.73718e-05	0.00294714	intron-variant	MED16	GRCh38.p7	19:881546	CGCGTGGCTGCCGCT[A/G]GCTCCACCGTACCGA	10025
rs754553007	snp	C/T	9.2614e-05	0.0068043	missense	MED16	GRCh38.p7	19:868930	GCAGGTGGTCGATCT[C/T]GGGCTGGCCTGGGGC	10025
rs754561721	in-del	-/G	6.18671e-05	0.00556145	intron-variant	MED16	GRCh38.p7	19:872154	TGTGGCTGGGGCGGC[-/G]GGGGGCAGATGGCGA	10025
rs754611022	snp	A/G	1.65408e-05	0.00287578	synonymous-codon, utr-variant-5-prime	MED16	GRCh38.p7	19:891078	TTTCTCCCACTCACA[A/G]ACGTAGGCCAAGTCC	10025
rs754655741	snp	C/T			intron-variant	MED16	GRCh38.p7	19:886828	CGCCTATAATCCCAG[C/T]ACTTTGGGGGGCTGA	10025
rs754670155	snp	A/G	3.34459e-05	0.00408924	synonymous-codon	MED16	GRCh38.p7	19:875284	CTCGGTCAGCCGGTC[A/G]CCGGGGCTCTTGTCA	10025
rs754689610	in-del	-/CGT			intron-variant	MED16	GRCh38.p7	19:878246	CCAGCCCCAGCCCCA[-/CGT]GCCCCAGCCCCACGG	10025
rs754726918	snp	C/T			intron-variant	MED16	GRCh38.p7	19:884582	CCCACGCTCCACAGC[C/T]GCCCACACGCCTGCA	10025
rs754739841	snp	A/G	1.94403e-05	0.00311766	synonymous-codon	MED16	GRCh38.p7	19:868155	GGGGGTCCTGGGAGA[A/G]TGGTGTGTGGACTGC	10025
rs754788476	snp	C/T	3.40536e-05	0.00412621	intron-variant	MED16	GRCh38.p7	19:886236	GGAGGAGGGGCCGCT[C/T]AGGCTCATGGGGGCT	10025
rs754802268	snp	G/T	1.90623e-05	0.0030872	missense	MED16	GRCh38.p7	19:880071	TCGGGGCCGCGGAGC[G/T]GTAGAAGACGGCCAT	10025
rs754849746	snp	A/G			intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:893063	CGTCCGCCCTCGCCG[A/G]GCCCCCGCAGCCCCG	10025
rs754866376	snp	G/T	1.72639e-05	0.00293796	missense	MED16	GRCh38.p7	19:872096	TCCCGCAGAAAGCTG[G/T]GGCCCGGCCTCAGCA	10025
rs754890014	snp	C/T	1.7182e-05	0.00293099	synonymous-codon, intron-variant	MED16	GRCh38.p7	19:877007	CTGGCGCGTGTACTC[C/T]TCGTGCAGCTTCTCC	10025
rs754921709	snp	C/G			intron-variant	MED16	GRCh38.p7	19:880461	GGCACTACAGGTGGG[C/G]GACCAAGGGTTGGGG	10025
rs754955836	snp	C/T	5.39622e-05	0.00519405	intron-variant	MED16	GRCh38.p7	19:890115	GGTCGCCACCCCTGG[C/T]CACGTGGGACCAGCG	10025
rs754993607	snp	A/C/G	9.35995e-05	0.00684047	intron-variant	MED16	GRCh38.p7	19:871614	CAGGTGCCTGGAAGT[A/C/G]GCTGCCATCCCAAAA	10025
rs755030363	in-del	-/CCAGCCCCG	0.000304105	0.0123272	intron-variant	MED16	GRCh38.p7	19:879904	GGTTGTCAATGCCCA[-/CCAGCCCCG]GCCCCACGTGCCCCA	10025
rs755031201	in-del	-/C	0.000161063	0.00897249	intron-variant	MED16	GRCh38.p7	19:886253	GGCTCATGGGGGCTG[-/C]CCCATGACCCCCAGA	10025
rs755044010	snp	A/G	4.53052e-05	0.00475926	intron-variant	MED16	GRCh38.p7	19:890258	GTCTGTGGGGACGGG[A/G]CATGGTCAGCACGGC	10025
rs755047145	snp	A/G	1.68863e-05	0.00290566	synonymous-codon	MED16	GRCh38.p7	19:868484	GGGCGACTTGAGCAT[A/G]GTGACACAGCCGCAC	10025
rs755065955	snp	A/G	1.92632e-05	0.00310342	missense	MED16	GRCh38.p7	19:880100	ATGGTCTGCAGTGAG[A/G]GCCGGTGCACGATGT	10025
rs755086892	snp	C/G/T	3.34282e-05	0.00408818	missense	MED16	GRCh38.p7	19:873514	GCAAGAGCTGCTGCA[C/G/T]CGCCTGCAGTGTGTT	10025
rs755113782	snp	A/G			missense	MED16	GRCh38.p7	19:886015	CGGCCAGGGCCACGC[A/G]GCCGCGCAGCCGGCA	10025
rs755155990	snp	A/C	1.69807e-05	0.00291377	missense, intron-variant	MED16	GRCh38.p7	19:877051	CCATACTGGGCTGCA[A/C]GTGCAGCAGGATGTC	10025
rs755170296	snp	A/G			upstream-variant-2KB	MED16	GRCh38.p7	19:894807	GAGGGAGGGGCGCTG[A/G]GCAAGGTGGTTCAGG	10025
rs755184337	snp	C/T	6.67802e-05	0.00577803	missense	MED16	GRCh38.p7	19:881640	GCTTGGGCAGCGCCA[C/T]GGCCGACACACGGTC	10025
rs755238542	in-del	-/AGGGGCAGCTG			intron-variant	MED16	GRCh38.p7	19:868325	GCAGCAGCCGGGCTC[-/AGGGGCAGCTG]AGGGGCAGCTGAGGG	10025
rs755249311	snp	A/G			intron-variant	MED16	GRCh38.p7	19:871261	ATCGCGACCTGCGGA[A/G]AGAGGTGGCGGAAGT	10025
rs755273483	in-del	-/TC			intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:892516	CCCAAATACGAGGCT[-/TC]ATCCCAGGGACCCCA	10025
rs755328735	snp	C/T			intron-variant	MED16	GRCh38.p7	19:881878	CCCGGCCAATCCGAG[C/T]GCTTCGTGCCTCGGC	10025
rs755355354	snp	A/C	0.000136883	0.00827181	missense	MED16	GRCh38.p7	19:871130	TGCTTGGGCTGCAGG[A/C]GGCTAACCAGGCCGT	10025
rs755376766	snp	A/C/G	3.44984e-05	0.0041531	intron-variant	MED16	GRCh38.p7	19:891163	TCCTGCGGGAGGGAG[A/C/G]TGTGGTGGGACGTCT	10025
rs755389475	snp	C/G	3.39657e-05	0.00412088	missense	MED16	GRCh38.p7	19:872001	AGGTGGCCGTATACA[C/G]GGGCAGGCAGCTGGG	10025
rs755456033	snp	C/G	4.43548e-05	0.00470908	missense	MED16	GRCh38.p7	19:879963	TGTCAATCCCCACCA[C/G]GGCCAGTGACGTCCA	10025
rs755460610	snp	A/C	1.74293e-05	0.00295201	missense, intron-variant	MED16	GRCh38.p7	19:889728	GCTGCCCACTGAGCT[A/C]TCCCAGCTATTAGCC	10025
rs755516666	snp	A/G	2.19411e-05	0.00331211	intron-variant	MED16	GRCh38.p7	19:872166	GGCGGGGGGCAGATG[A/G]CGATGGGATGAAGTG	10025
rs755523224	in-del	-/GAGAGGGGAGGGGCGGGCGGGGGA	2.45516e-05	0.0035036	intron-variant	MED16	GRCh38.p7	19:871894	AGAGCGGGGAGCGGG[-/GAGAGGGGAGGGGCGGGCGGGGGA]GAGAGGGGAGGGGCG	10025
rs755536543	in-del	-/G			upstream-variant-2KB, nc-transcript-variant	MED16, RNU6-9	GRCh38.p7	19:893536	ATACAGAGAAGATTA[-/G]GCATGGCCCCTGCGC	10025
rs755567635	snp	A/G			intron-variant	MED16	GRCh38.p7	19:888615	AAACCTCTGGACCGT[A/G]TGGGCTGCACACTCT	10025
rs755635553	in-del	-/TT			upstream-variant-2KB, nc-transcript-variant	MED16, RNU6-9	GRCh38.p7	19:893587	TGAAGCGTTCCATAT[-/TT]TTTTTTTTTTTTCCA	10025
rs755643455	snp	A/G	0.00059755	0.0172748	intron-variant	MED16	GRCh38.p7	19:873052	GGGGCAGGGCTCCGA[A/G]GTGGGGCAGGGCTCC	10025
rs755653397	snp	C/T	2.01217e-05	0.00317182	missense, intron-variant	MED16	GRCh38.p7	19:877151	CTCCAGCGGGTGGCC[C/T]ATGGAAGGTGAGAGG	10025
rs755675112	snp	A/G	9.11951e-05	0.00675198	intron-variant	MED16	GRCh38.p7	19:880151	GCCAGGGCCAGCCCT[A/G]TGGGGCACAGGCACT	10025
rs755678877	snp	C/T	5.01953e-05	0.00500951	missense	MED16	GRCh38.p7	19:885790	CCGACATGTCCCGGG[C/T]CAGGAACTTGAGGTG	10025
rs755693304	snp	A/G	0.000121068	0.00777941	intron-variant	MED16	GRCh38.p7	19:880195	CAGGGCCCAGGACAC[A/G]CCCGCCGGGGGAGGG	10025
rs755757971	snp	A/G	0.000137758	0.00829818	synonymous-codon	MED16	GRCh38.p7	19:885953	CGACGCGCTGCTGCC[A/G]TCCGCCGTGGCCACC	10025
rs755759140	snp	C/T			intron-variant	MED16	GRCh38.p7	19:883373	GGTGGGCACGTGGGG[C/T]GGTGGGTGAAGAGCT	10025
rs755795385	snp	A/G	1.94037e-05	0.00311472	intron-variant	MED16	GRCh38.p7	19:868845	CTCTGGGAGTCAGCG[A/G]TTCCGGGGGCCCCTC	10025
rs755810516	snp	C/T	2.46412e-05	0.00350998	synonymous-codon, intron-variant	MED16	GRCh38.p7	19:877178	GAGGCGGAGCACGCT[C/T]AGCTGCCAGAGACAG	10025
rs755820828	snp	C/T	1.92992e-05	0.00310632	intron-variant	MED16	GRCh38.p7	19:871699	AGGCAGAGCCACTGC[C/T]ACCTGCAGGGGCTTA	10025
rs755829220	in-del	-/TCCCGGAGG			intron-variant	MED16	GRCh38.p7	19:869639	CAAGCCAGGGCGCCT[-/TCCCGGAGG]TCCCGGAGCCAAGCC	10025
rs755844250	snp	C/G	3.51031e-05	0.00418931	missense	MED16	GRCh38.p7	19:868919	GTGCAGCCTCCGCAG[C/G]TGGTCGATCTTGGGC	10025
rs755872270	snp	C/G	2.15292e-05	0.00328088	synonymous-codon, utr-variant-5-prime	MED16	GRCh38.p7	19:886163	CGACGGTGAGAACTT[C/G]ACTCGGGAGAACTTC	10025
rs755929712	snp	A/G	1.97826e-05	0.00314498	missense	MED16	GRCh38.p7	19:886107	CCGCTGACCGTCACC[A/G]CGATCCAGCCCTCCA	10025
rs755971535	snp	A/G	1.6701e-05	0.00288968	missense, utr-variant-5-prime	MED16	GRCh38.p7	19:890978	CCTGGTCATCGCTGC[A/G]CAGGTCCATGGTGAA	10025
rs755992023	snp	G/T			intron-variant	MED16	GRCh38.p7	19:877509	GAAGCTCCTAATACG[G/T]GCTGTGAGCCACCCC	10025
rs756043257	snp	C/T	3.58661e-05	0.00423459	synonymous-codon	MED16	GRCh38.p7	19:868113	CCGTCACGGACGGTC[C/T]TCTGGATGCAGATGG	10025
rs756101278	snp	G/T	3.38244e-05	0.0041123	missense	MED16	GRCh38.p7	19:872061	CCATCAATTCCCGAA[G/T]CATGCCCAGCGAGGT	10025
rs756104765	in-del	-/AG	5.2063e-05	0.00510184	intron-variant	MED16	GRCh38.p7	19:877186	GCACGCTCAGCTGCC[-/AG]AGACAGAGCCCAAGG	10025
rs756154118	snp	A/G	4.21763e-05	0.00459199	intron-variant	MED16	GRCh38.p7	19:871266	GACCTGCGGAGAGAG[A/G]TGGCGGAAGTCTCAG	10025
rs756154373	snp	A/C/G	3.42902e-05	0.00414055	missense	MED16	GRCh38.p7	19:872090	GTGCCGTCCCGCAGA[A/C/G]AGCTGTGGCCCGGCC	10025
rs756195955	snp	A/G	2.26673e-05	0.00336647	synonymous-codon	MED16	GRCh38.p7	19:884940	GATGTTGTTCACGGG[A/G]AGTCCCTCCTTGCGC	10025
rs756207250	snp	A/G	3.85996e-05	0.00439298	intron-variant	MED16	GRCh38.p7	19:871583	TACACACAACCCGAC[A/G]AGGAGAGACAGCAAA	10025
rs756218393	snp	A/C	8.87535e-05	0.00666099	intron-variant	MED16	GRCh38.p7	19:890105	CCGGGATCCGGGTCG[A/C]CACCCCTGGCCACGT	10025
rs756227651	snp	C/G/T	3.96222e-05	0.00445082	intron-variant	MED16	GRCh38.p7	19:876963	GGGCCCCACCTGCCA[C/G/T]GGGCCCCCACCTGCT	10025
rs756237341	snp	A/G	0.000120897	0.00777393	intron-variant	MED16	GRCh38.p7	19:890250	CGGGTCAGGTCTGTG[A/G]GGACGGGGCATGGTC	10025
rs756281329	snp	C/G	1.91848e-05	0.0030971	missense	MED16	GRCh38.p7	19:880064	ACAGGCCTCGGGGCC[C/G]CGGAGCTGTAGAAGA	10025
rs756352731	snp	A/G	5.00488e-05	0.00500219	synonymous-codon	MED16	GRCh38.p7	19:885884	CAGGATCTCCGTGTC[A/G]ATACGGCACTTCTCG	10025
rs756496919	snp	A/C/G/T	0.000126413	0.00794947	synonymous-codon, missense	MED16	GRCh38.p7	19:871930	GGGTGCCTCACAGCA[A/C/G/T]ATCCAGAGCTTGGTG	10025
rs756514182	snp	C/T	5.13281e-05	0.00506571	missense	MED16	GRCh38.p7	19:881559	CTGGCTCCACCGTAC[C/T]GAGGCCAGGGTAGAA	10025
rs756532217	snp	C/T	1.6679e-05	0.00288777	synonymous-codon	MED16	GRCh38.p7	19:873545	CATGTCCAGCACAAA[C/T]TCCTCCGTCTTGAGG	10025
rs756603391	snp	C/T			intron-variant	MED16	GRCh38.p7	19:882612	GAGGGCAGCTGGAGC[C/T]GGCCTGCTGGAGCAT	10025
rs756603879	snp	A/G	1.67022e-05	0.00288978	missense	MED16	GRCh38.p7	19:881621	TTGGTGAGCGAGATG[A/G]GCAGCTTGGGCAGCG	10025
rs756658898	snp	C/T	1.68131e-05	0.00289935	missense, utr-variant-5-prime	MED16	GRCh38.p7	19:891127	GGCCGCCGCAAATCA[C/T]ACATGAGGGCAGTCA	10025
rs756660089	snp	C/T	1.66765e-05	0.00288756	missense	MED16	GRCh38.p7	19:875352	GGGTGGAGCTGATGG[C/T]GATGAGGAAGAGCTT	10025
rs756660505	snp	C/T			intron-variant	MED16	GRCh38.p7	19:890332	CTCCAGGTAAGCCGG[C/T]GTGTGTCCCACCCCA	10025
rs756668412	snp	A/G	8.04236e-05	0.00634077	stop-gained	MED16	GRCh38.p7	19:871125	GGGGCTGCTTGGGCT[A/G]CAGGCGGCTAACCAG	10025
rs756685364	snp	C/T			intron-variant	MED16	GRCh38.p7	19:883640	GCCAGCAGGTGAGGA[C/T]GGCTGCAGGAGACGA	10025
rs756733557	snp	A/G	4.00088e-05	0.00447245	intron-variant	MED16	GRCh38.p7	19:885024	CTGCGGGGGAGGTGG[A/G]GGTGAGGGCTGACCC	10025
rs756758577	snp	C/T	1.70214e-05	0.00291726	synonymous-codon, intron-variant	MED16	GRCh38.p7	19:889644	GACACTCACCTTCTC[C/T]ACGTGCAGGGCCAGT	10025
rs756770436	snp	C/T	0.000291468	0.0120685	missense, intron-variant	MED16	GRCh38.p7	19:889706	CAATGGGGTCCCCCT[C/T]CACTAGGCTGCCCAC	10025
rs756786376	snp	C/T	1.68527e-05	0.00290277	missense	MED16	GRCh38.p7	19:875397	ACACGCGGGTCACCG[C/T]GCAGGGCGACAGCTT	10025
rs756790351	snp	C/T			intron-variant	MED16	GRCh38.p7	19:890432	AGCAGGCCTGTGAGG[C/T]GCCACAACTGTGTCT	10025
rs756795318	snp	A/G			intron-variant	MED16	GRCh38.p7	19:882658	AGGCCACGCCACCTC[A/G]GCTGCTAACCGCAGA	10025
rs756855793	snp	A/G			synonymous-codon	MED16	GRCh38.p7	19:868922	CAGCCTCCGCAGGTG[A/G]TCGATCTTGGGCTGG	10025
rs756891733	snp	C/T	1.64944e-05	0.00287175	intron-variant	MED16	GRCh38.p7	19:885726	TGAGAAGCAGTGCTT[C/T]ATTCCAAGCCTGCCA	10025
rs756905239	snp	A/T			intron-variant	MED16	GRCh38.p7	19:876423	CAGGGCCACCGGGTG[A/T]GCATCCTGGTACCCA	10025
rs756989326	snp	C/G/T	1.88642e-05	0.00307111	intron-variant	MED16	GRCh38.p7	19:871672	TAGGAACTGGGGAAA[C/G/T]AGCAGATATCAAGGC	10025
rs757020424	in-del	-/TCCCAC	0.000254723	0.0112826	cds-indel, intron-variant	MED16	GRCh38.p7	19:877054	ACTGGGCTGCACGTG[-/TCCCAC]CAGCAGGATGTCCCA	10025
rs757020591	snp	C/G	1.72104e-05	0.00293341	intron-variant	MED16	GRCh38.p7	19:868535	AGCGGGTTCCCACTT[C/G]CAGGCGGGCCTCCCT	10025
rs757029978	snp	A/G			intron-variant	MED16	GRCh38.p7	19:870334	GGGAGGGCGAGGCAG[A/G]TGGATCACCTGAGGT	10025
rs757084189	snp	A/G	2.00531e-05	0.00316641	synonymous-codon	MED16	GRCh38.p7	19:886034	GCGCAGCCGGCACAG[A/G]CTCTCGGTGGACGTC	10025
rs757104731	snp	A/G			intron-variant	MED16	GRCh38.p7	19:875957	CTCTACAAAAAATAG[A/G]AACAACTAAAAACAA	10025
rs757122313	snp	A/G	0.000281747	0.0118657	synonymous-codon, utr-variant-5-prime	MED16	GRCh38.p7	19:886136	CATGGGCTTGCCGCC[A/G]AACAGCGTGAGCGAC	10025
rs757139920	snp	A/G	0.000100326	0.00708188	intron-variant	MED16	GRCh38.p7	19:868838	GGCACATCTCTGGGA[A/G]TCAGCGGTTCCGGGG	10025
rs757212982	snp	A/G	1.86451e-05	0.00305323	utr-variant-3-prime	MED16	GRCh38.p7	19:868056	AAGGAAACCGAGGAG[A/G]CGCCCGAGCCGGGTC	10025
rs757223668	snp	C/T			intron-variant	MED16	GRCh38.p7	19:877456	TACCTGAGGAGTCTA[C/T]CCCGTGAAAGGCGGT	10025
rs757251673	in-del	-/C			intron-variant	MED16	GRCh38.p7	19:869929	GGTGACAAGGTCCCA[-/C]CCCTTTCCAGGCTGG	10025
rs757267674	snp	A/G	7.00783e-05	0.00591897	intron-variant	MED16	GRCh38.p7	19:875224	AAACCTCGAGGCCCC[A/G]GGCGTGGAAAAGGAC	10025
rs757297917	snp	A/G			intron-variant	MED16	GRCh38.p7	19:884856	AAATAAAAACCAACC[A/G]CCCCCGAGGGCAGGC	10025
rs757366351	snp	C/T			intron-variant	MED16	GRCh38.p7	19:869525	ACCGTCCTCTCTTTC[C/T]ATCAAGTCTTTTCCT	10025
rs757403542	snp	A/G	9.7334e-05	0.0069755	missense	MED16	GRCh38.p7	19:880029	CCGCGGTGCGGGGGC[A/G]CTTCATGGCCGGCTC	10025
rs757415642	snp	C/G/T	3.38051e-05	0.00411116	missense	MED16	GRCh38.p7	19:872057	ACCACCATCAATTCC[C/G/T]GAAGCATGCCCAGCG	10025
rs757433510	snp	C/T	2.04055e-05	0.00319411	intron-variant	MED16	GRCh38.p7	19:876957	GCCACGGGGCCCCAC[C/T]TGCCACGGGCCCCCA	10025
rs757462927	in-del	-/G			intron-variant	MED16	GRCh38.p7	19:887881	AGGGTGATGCAGGAT[-/G]GGGACTGGGTTTCCT	10025
rs757492010	snp	C/G			intron-variant	MED16	GRCh38.p7	19:888193	TGGGCAACAGAGCAA[C/G]ACCCTGTCTCAAAAA	10025
rs757553366	snp	C/T	1.86632e-05	0.00305471	intron-variant	MED16	GRCh38.p7	19:868400	GAGGGGCACCCGCCA[C/T]CAGAGCCCACCGCAC	10025
rs757565226	snp	A/G			intron-variant	MED16	GRCh38.p7	19:876617	GACGGGCCTCTGGGA[A/G]CACACCCCACACGCA	10025
rs757571723	in-del	-/TGCG			intron-variant	MED16	GRCh38.p7	19:882782	TTACTCGGCTGAAGC[-/TGCG]TGACTACCACGCAGC	10025
rs757580891	snp	G/T			intron-variant	MED16	GRCh38.p7	19:890457	GTGTCTTTAAAACCA[G/T]ATTAGAAGAAAATGA	10025
rs757591958	snp	A/G			downstream-variant-500B	MED16	GRCh38.p7	19:867553	AAACTTGGCCCAGGG[A/G]CTAAGCAACCTCCAG	10025
rs757603192	snp	A/G	2.25207e-05	0.00335557	intron-variant	MED16	GRCh38.p7	19:889810	AGGAGCCGGGAGCCT[A/G]AGGGCAAGAAGCCAT	10025
rs757630295	snp	A/G	1.7149e-05	0.00292817	intron-variant	MED16	GRCh38.p7	19:873436	CGGGGCCTTAGGGGA[A/G]AGCATGGCGCACCTG	10025
rs757633448	snp	A/G	0.375	0.216506	intron-variant	MED16	GRCh38.p7	19:872965	GGAGGGCTCCGAGGT[A/G]GGGCAGGGCTCCGAG	10025
rs757692788	snp	A/G	5.00079e-05	0.00500015	synonymous-codon	MED16	GRCh38.p7	19:885812	CTTGAGGTGGGTGAT[A/G]GCGGGAAACTTGTCC	10025
rs757719334	snp	C/T			intron-variant	MED16	GRCh38.p7	19:871624	GAAGTGGCTGCCATC[C/T]CAAAAGCACCCACAC	10025
rs757743210	snp	A/C	1.72692e-05	0.00293842	intron-variant	MED16	GRCh38.p7	19:881552	GCTGCCGCTGGCTCC[A/C]CCGTACCGAGGCCAG	10025
rs757761207	snp	C/T	1.68108e-05	0.00289916	missense	MED16	GRCh38.p7	19:873481	CCAGCAGGTACAGCA[C/T]GAAGTCGCCCACCCA	10025
rs757819639	snp	A/G	7.83039e-05	0.00625666	intron-variant	MED16	GRCh38.p7	19:871708	CACTGCCACCTGCAG[A/G]GGCTTATGTTCTGGC	10025
rs757826255	snp	C/T	3.34135e-05	0.00408725	synonymous-codon	MED16	GRCh38.p7	19:881614	GTCGGTGTTGGTGAG[C/T]GAGATGGGCAGCTTG	10025
rs757852933	snp	A/G	3.92842e-05	0.00443177	intron-variant	MED16	GRCh38.p7	19:886249	CTCAGGCTCATGGGG[A/G]CTGCCCCATGACCCC	10025
rs757870956	snp	A/C	3.39438e-05	0.00411955	intron-variant	MED16	GRCh38.p7	19:871921	GGCGGGCGGGGGTGC[A/C]TCACAGCAGATCCAG	10025
rs757877270	snp	C/T			intron-variant	MED16	GRCh38.p7	19:873715	GACCCACACCGGGAA[C/T]GAGAAGGGGGCGATG	10025
rs757895311	snp	C/T			intron-variant	MED16	GRCh38.p7	19:886947	AGCCGGGCATGGTAG[C/T]GGGTGCCTATAATCC	10025
rs757928053	snp	A/G	0.000182	0.00953766	intron-variant	MED16	GRCh38.p7	19:871013	GAGTCCTGTGTTTGG[A/G]GACCAATGCAGGGAC	10025
rs757928487	snp	C/G			intron-variant	MED16	GRCh38.p7	19:883127	CCAACTGACGGCTGC[C/G]GTCAGCATTCCTAAA	10025
rs757941925	snp	C/G	1.66815e-05	0.00288799	missense	MED16	GRCh38.p7	19:875296	GTCGCCGGGGCTCTT[C/G]TCAGGCGTGTTGAGA	10025
rs757979642	snp	A/G	3.9681e-05	0.00445409	missense	MED16	GRCh38.p7	19:868160	TCCTGGGAGAGTGGT[A/G]TGTGGACTGCGGGCC	10025
rs757997027	snp	A/C	3.33428e-05	0.00408293	missense	MED16	GRCh38.p7	19:875345	GACTTCAGGGTGGAG[A/C]TGATGGCGATGAGGA	10025
rs758021147	snp	A/G	1.72612e-05	0.00293774	intron-variant	MED16	GRCh38.p7	19:889632	TCACTCGGGCAGGAC[A/G]CTCACCTTCTCCACG	10025
rs758049973	snp	A/C/G	3.70029e-05	0.0043012	intron-variant	MED16	GRCh38.p7	19:872131	ACCCTGCCCGAAAGA[A/C/G]GCATCGGTGTGGCTG	10025
rs758058610	snp	A/C			intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:892672	CTCCAGGCCCCGCAC[A/C]GATAACCCCGCAGTC	10025
rs758075353	snp	C/T	0.000119333	0.00772349	missense	MED16	GRCh38.p7	19:884972	GGGACCAGCACTCCA[C/T]GATGCTGCTGGTCTG	10025
rs758121169	snp	A/G	0.00128813	0.0253457	synonymous-codon	MED16	GRCh38.p7	19:868221	AGCTCTGCTGGTCAC[A/G]CAGGCGTCCGGCCCA	10025
rs758125469	in-del	-/CCC	9.51716e-05	0.00689759	intron-variant	MED16	GRCh38.p7	19:876933	CCACCTGCCACAGGG[-/CCC]CCACCTGCCACGGGG	10025
rs758183548	snp	A/G			intron-variant	MED16	GRCh38.p7	19:890873	GTGGCCTGAGAGACC[A/G]AGTCCCTTCAAGGCA	10025
rs758188091	in-del	-/GGGGGGACCTGGGGCAGGACATGCAGGGAGGGAGCCGTGTGGATT			intron-variant	MED16	GRCh38.p7	19:870923	GAGCCGTGTGGATTC[lengthTooLong]CGGGGGTCCCGGGGC	10025
rs758193267	snp	A/T	0.000131935	0.00812096	intron-variant	MED16	GRCh38.p7	19:890261	TGTGGGGACGGGGCA[A/T]GGTCAGCACGGCCTG	10025
rs758197797	in-del	-/GGTGG	0.00100604	0.0224055	intron-variant	MED16	GRCh38.p7	19:872980	GGGGCAGGGCTCCGA[-/GGTGG]GGGAGGGCTCCGAGG	10025
rs758248505	snp	A/G	2.06981e-05	0.00321693	intron-variant	MED16	GRCh38.p7	19:872156	TGGCTGGGGCGGCGG[A/G]GGGCAGATGGCGATG	10025
rs758268465	snp	C/T	1.86942e-05	0.00305725	intron-variant	MED16	GRCh38.p7	19:871616	GGTGCCTGGAAGTGG[C/T]TGCCATCCCAAAAGC	10025
rs758326837	snp	C/G	1.94638e-05	0.00311954	synonymous-codon	MED16	GRCh38.p7	19:880108	CAGTGAGAGCCGGTG[C/G]ACGATGTGGACGCTG	10025
rs758330092	in-del	-/GGGGAGA			intron-variant	MED16	GRCh38.p7	19:871768	TAGGGAGAGGGGAGC[-/GGGGAGA]GGGGAGAGGGGAGAG	10025
rs758345250	snp	A/G	0.000186927	0.00966584	synonymous-codon, intron-variant	MED16	GRCh38.p7	19:877061	CTGCACGTGCAGCAG[A/G]ATGTCCCACCAGTCG	10025
rs758369248	snp	C/G/T			intron-variant	MED16	GRCh38.p7	19:876049	CTAGCGCTGTCACTG[C/G/T]CTACGGATCCCAGCC	10025
rs758487854	snp	A/G	7.97703e-05	0.00631496	synonymous-codon	MED16	GRCh38.p7	19:886094	CACGGTGACCAGGCC[A/G]CTGACCGTCACCGCG	10025
rs758494170	snp	A/G			intron-variant	MED16	GRCh38.p7	19:876566	AAACTTCCCAGGTAA[A/G]GAAGGAAACTGCTTC	10025
rs758539378	snp	C/T	1.75019e-05	0.00295815	missense	MED16	GRCh38.p7	19:871971	AGAGCAGGGACATGC[C/T]GTCCTGGGTATCCGA	10025
rs758622952	snp	C/T	1.69714e-05	0.00291298	synonymous-codon	MED16	GRCh38.p7	19:872005	GGCCGTATACACGGG[C/T]AGGCAGCTGGGCTTC	10025
rs758677436	snp	A/T			intron-variant	MED16	GRCh38.p7	19:870161	AGGCGTCTCTCTCCA[A/T]CCACAGAGGGATCTA	10025
rs758685057	snp	A/G	5.29946e-05	0.00514728	missense, intron-variant	MED16	GRCh38.p7	19:889741	CTCTCCCAGCTATTA[A/G]CCAGGTGGTCCGCCA	10025
rs758696704	snp	A/T			intron-variant	MED16	GRCh38.p7	19:889287	AGAGGGTGGGCTGCA[A/T]TCAGAAGACAGCAGC	10025
rs758701379	snp	C/T	1.74117e-05	0.00295052	intron-variant	MED16	GRCh38.p7	19:885747	AAGCCTGCCAGCCCA[C/T]GTGATGGCCTGCGCC	10025
rs758736704	in-del	-/GGGAGGGGAAGCAGGT	1.79033e-05	0.00299188	intron-variant	MED16	GRCh38.p7	19:890931	GGACACCATGCGGCC[-/GGGAGGGGAAGCAGGT]GGGAGGGGAAGCAGG	10025
rs758743265	snp	A/G	1.74017e-05	0.00294967	intron-variant	MED16	GRCh38.p7	19:891172	AGGGAGGTGTGGTGG[A/G]ACGTCTATGTTGGCT	10025
rs758773354	snp	A/G			utr-variant-3-prime	MED16	GRCh38.p7	19:868016	CCGCTGCTTGTCCAG[A/G]TTCAGCGCTCTCCGC	10025
rs758794901	snp	A/G	2.12033e-05	0.00325595	missense, intron-variant	MED16	GRCh38.p7	19:889799	CATCTGCTGACAGGA[A/G]CCGGGAGCCTGAGGG	10025
rs758871448	in-del	-/GAAGTGGCTGCCATCC	1.88225e-05	0.00306772	intron-variant	MED16	GRCh38.p7	19:871609	GCAAACAGGTGCCTG[-/GAAGTGGCTGCCATCC]CAAAAGCACCCACAC	10025
rs758871867	snp	A/G	3.05871e-05	0.00391058	intron-variant	MED16	GRCh38.p7	19:875486	AGGTCACCCCAAGGG[A/G]CCGGAGCAGAGGCGC	10025
rs758888374	snp	A/G	0.000562911	0.0167672	intron-variant	MED16	GRCh38.p7	19:876947	GCCCCCACCTGCCAC[A/G]GGGCCCCACCTGCCA	10025
rs758891329	snp	C/G	1.66854e-05	0.00288833	missense	MED16	GRCh38.p7	19:885805	CCAGGAACTTGAGGT[C/G]GGTGATGGCGGGAAA	10025
rs758906090	snp	G/T	2.48982e-05	0.00352824	intron-variant	MED16	GRCh38.p7	19:868341	AGGGGCAGCTGAGGG[G/T]TAGCTGAGGAGTAGC	10025
rs758923298	snp	G/T	1.79997e-05	0.00299992	intron-variant	MED16	GRCh38.p7	19:873398	AAGCGGGGTCCTGAT[G/T]AGATGGGGGCCCAGG	10025
rs758937981	snp	A/G	8.32397e-05	0.00645081	synonymous-codon	MED16	GRCh38.p7	19:885862	TGCAGCGCATGAACA[A/G]GGAGGGCAGGATCTC	10025
rs758949287	snp	A/C/T	3.79739e-05	0.00435727	intron-variant	MED16	GRCh38.p7	19:871681	GGGAAATAGCAGATA[A/C/T]CAAGGCAGAGCCACT	10025
rs758978961	snp	A/G/T	3.43892e-05	0.00414652	intron-variant	MED16	GRCh38.p7	19:873433	GGGCGGGGCCTTAGG[A/G/T]GAGAGCATGGCGCAC	10025
rs758997251	snp	A/C			intron-variant	MED16	GRCh38.p7	19:872388	CTCTGGCTGAGGCCA[A/C]TATCCCCACCTGCAC	10025
rs759048157	snp	C/T	8.8248e-05	0.006642	missense	MED16	GRCh38.p7	19:885985	CGATGTTGCCGCCGC[C/T]GGTGAAGGCGATGTC	10025
rs759054980	in-del	-/GGGCCCCCACCTGCCACGGGGCCCCACCTGCCACG	7.89141e-05	0.00628099	intron-variant	MED16	GRCh38.p7	19:876930	CCCCCACCTGCCACA[lengthTooLong]GGCCCCCACCTGCTG	10025
rs759056716	snp	A/G			intron-variant	MED16	GRCh38.p7	19:890301	CCTGCAGACGATGAC[A/G]ATGACTCCAGGCAGG	10025
rs759071164	snp	A/C			intron-variant	MED16	GRCh38.p7	19:875805	AGGCTGCTCCAGCCC[A/C]CGATGTCTGTGGTGC	10025
rs759087690	snp	C/T	9.44956e-05	0.00687305	missense, utr-variant-5-prime	MED16	GRCh38.p7	19:890170	GGCAGGTGATGGCCT[C/T]GTGGTGCTCTGAGGG	10025
rs759126722	snp	A/T	1.67184e-05	0.00289118	missense	MED16	GRCh38.p7	19:881604	CCACCTTGAGGTCGG[A/T]GTTGGTGAGCGAGAT	10025
rs759128500	snp	A/G	1.72487e-05	0.00293667	intron-variant	MED16	GRCh38.p7	19:885753	GCCAGCCCACGTGAT[A/G]GCCTGCGCCCGTTCA	10025
rs759134103	snp	A/C/G	5.00967e-05	0.00500462	missense	MED16	GRCh38.p7	19:881661	ACACACGGTCCAGAT[A/C/G]GTTGGTGGCCGATAG	10025
rs759143794	snp	G/T	1.6918e-05	0.00290839	missense	MED16	GRCh38.p7	19:885937	TGTAGAACTGCACGG[G/T]CGACGCGCTGCTGCC	10025
rs759144770	snp	C/T			intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:892139	GGCATCCAGACGGGC[C/T]GTTTCGCTTCGCAAA	10025
rs759160543	snp	A/C			upstream-variant-2KB, downstream-variant-500B	MED16, RNU6-9	GRCh38.p7	19:893700	CCTCCCGGGTTGAAG[A/C]GATTCTCCTGCCTCA	10025
rs759212514	snp	A/C	6.7514e-05	0.00580968	intron-variant	MED16	GRCh38.p7	19:879895	CCTTCCCCTGGTTGT[A/C]AATGCCCACCAGCCC	10025
rs759246419	snp	G/T	1.66654e-05	0.00288659	synonymous-codon, utr-variant-5-prime	MED16	GRCh38.p7	19:891111	CATCCCACCTGCCGC[G/T]GGCCGCCGCAAATCA	10025
rs759290119	snp	A/C			intron-variant	MED16	GRCh38.p7	19:870397	AAAACCGCCTCTATA[A/C]CAAAAATACAAAAAA	10025
rs759314391	snp	A/G	3.33383e-05	0.00408265	missense	MED16	GRCh38.p7	19:875339	AGCAGCGACTTCAGG[A/G]TGGAGCTGATGGCGA	10025
rs759368223	snp	C/T	2.50818e-05	0.00354123	missense	MED16	GRCh38.p7	19:879941	CAGCAGCTCACCTTC[C/T]CGTGGCTGTCAATCC	10025
rs759373885	snp	A/C/G			intron-variant	MED16	GRCh38.p7	19:888815	TGGGGAGGGACTCAC[A/C/G]AAGGGACGAGAGAAA	10025
rs759381959	snp	A/G	5.2633e-05	0.00512969	missense	MED16	GRCh38.p7	19:868207	GGGGCTTCCTCAGAA[A/G]CTCTGCTGGTCACGC	10025
rs759451733	in-del	-/A			intron-variant	MED16	GRCh38.p7	19:890560	AATTTTCTGTGGTTT[-/A]TCTAGTTTTCTCTAA	10025
rs759500855	snp	C/G	1.65754e-05	0.00287879	synonymous-codon	MED16	GRCh38.p7	19:875452	GATCCGGGTGGAGAG[C/G]ACCTGAGGGCAGGAA	10025
rs759507647	snp	A/G	3.61109e-05	0.00424901	intron-variant	MED16	GRCh38.p7	19:885015	CAAAAGCACCTGCGG[A/G]GGAGGTGGGGGTGAG	10025
rs759507737	snp	A/C/T	5.12556e-05	0.00506218	synonymous-codon, intron-variant	MED16	GRCh38.p7	19:889701	GGCCACAATGGGGTC[A/C/T]CCCTCCACTAGGCTG	10025
rs759548933	snp	A/C/G	0.000186048	0.00964332	intron-variant	MED16	GRCh38.p7	19:872154	TGTGGCTGGGGCGGC[A/C/G]GGGGGCAGATGGCGA	10025
rs759622871	snp	C/T	0.000127101	0.00797083	synonymous-codon, intron-variant	MED16	GRCh38.p7	19:877127	CAGGTGCCGCAGCGC[C/T]AGCCCCACCTCCAGC	10025
rs759624549	snp	A/G			intron-variant	MED16	GRCh38.p7	19:873961	GCTGCAGCCACCCCC[A/G]GCTGGCAGCTGGCGG	10025
rs759713678	snp	A/C/T	3.61456e-05	0.00425109	intron-variant	MED16	GRCh38.p7	19:890920	GGGAACAGGGCGGGA[A/C/T]ACCATGCGGCCGGGA	10025
rs759719220	snp	A/G			intron-variant	MED16	GRCh38.p7	19:884674	ATGGTGGCAGCCGCC[A/G]CAGCGGGCGTGGAAG	10025
rs759793017	snp	A/G			intron-variant	MED16	GRCh38.p7	19:890686	AGAAAACTGGGGCAC[A/G]TGTCTCCAACAAGCC	10025
rs759819731	in-del	-/ACAC	1.95961e-05	0.00313012	intron-variant	MED16	GRCh38.p7	19:871569	TCACCCTCCTCACAT[-/ACAC]ACAACCCGACAAGGA	10025
rs759882318	snp	G/T	1.76027e-05	0.00296665	intron-variant	MED16	GRCh38.p7	19:868550	CCAGGCGGGCCTCCC[G/T]TACGCCTGCCCCACT	10025
rs759896910	snp	C/T	1.65963e-05	0.0028806	intron-variant	MED16	GRCh38.p7	19:884884	GGCCCAGGGCCTCCG[C/T]AGCCGGCGGGAGACT	10025
rs759922229	snp	A/G	2.00058e-05	0.00316267	synonymous-codon	MED16	GRCh38.p7	19:886085	CAGCAGGGACACGGT[A/G]ACCAGGCCGCTGACC	10025
rs759950566	snp	C/T	3.95124e-05	0.00444462	intron-variant	MED16	GRCh38.p7	19:875199	TAAAAATAAAATAAA[C/T]AGATGAAAGAAACCT	10025
rs759967376	snp	A/G			synonymous-codon, utr-variant-5-prime	MED16	GRCh38.p7	19:890171	GCAGGTGATGGCCTC[A/G]TGGTGCTCTGAGGGG	10025
rs759978778	snp	C/T	3.86153e-05	0.00439388	missense	MED16	GRCh38.p7	19:871248	TCGCTGGGCCCTCAT[C/T]GCGACCTGCGGAGAG	10025
rs760070634	snp	G/T	3.99497e-05	0.00446914	synonymous-codon, intron-variant	MED16	GRCh38.p7	19:889788	CTGCCCGTCGGCATC[G/T]GCTGACAGGAGCCGG	10025
rs760106131	snp	G/T			upstream-variant-2KB	MED16	GRCh38.p7	19:894478	GGCCTCACTGCATGA[G/T]TTTTGCAAGAATTCT	10025
rs760119634	snp	A/G			intron-variant	MED16	GRCh38.p7	19:887265	TGGTGAGGGGTTGCC[A/G]TGGCGACGACTCATC	10025
rs760147614	snp	C/T	7.8284e-05	0.00625587	missense	MED16	GRCh38.p7	19:880022	GCGGGGCCCGCGGTG[C/T]GGGGGCGCTTCATGG	10025
rs760273087	snp	C/G	1.6855e-05	0.00290297	synonymous-codon	MED16	GRCh38.p7	19:873470	GGGTAGGCTGGCCAG[C/G]AGGTACAGCACGAAG	10025
rs760290167	snp	A/C/G	5.7619e-05	0.0053672	intron-variant	MED16	GRCh38.p7	19:889844	TGCGAACCTTCCAGG[A/C/G]ATGGGCAGAGCACTG	10025
rs760305285	snp	C/T	1.92803e-05	0.0031048	missense	MED16	GRCh38.p7	19:880055	GGCTCATCCACAGGC[C/T]TCGGGGCCGCGGAGC	10025
rs760325527	snp	C/T			intron-variant	MED16	GRCh38.p7	19:876928	GGCCCCCACCTGCCA[C/T]AGGGCCCCCACCTGC	10025
rs760341396	in-del	-/G			intron-variant	MED16	GRCh38.p7	19:876550	TAACGTGTTACAGAA[-/G]AAACTTCCCAGGTAA	10025
rs760348619	snp	A/C			intron-variant	MED16	GRCh38.p7	19:881506	TGTGCTCAGGGCCCA[A/C]CTCCCCTGGTGTGAA	10025
rs760359642	snp	C/G	6.02283e-05	0.0054873	intron-variant	MED16	GRCh38.p7	19:868389	CAGGGGTAGCTGAGG[C/G]GCACCCGCCACCAGA	10025
rs760376011	snp	C/T			intron-variant	MED16	GRCh38.p7	19:886538	TGGTCCCTGTTGCAA[C/T]GACTTGGCTCTGGCT	10025
rs760393134	snp	C/T	5.58249e-05	0.00528293	missense, intron-variant	MED16	GRCh38.p7	19:876978	CGGGCCCCCACCTGC[C/T]GCAGGGCAGCGGTCT	10025
rs760407689	snp	A/G			upstream-variant-2KB	MED16	GRCh38.p7	19:894449	GTGCTGGGATTATAG[A/G]CGTGAGCCACCGCGG	10025
rs760505191	snp	C/G			intron-variant	MED16	GRCh38.p7	19:872213	ACCCCGACCGGGGGG[C/G]AATGGGCAGGGTCTG	10025
rs760562564	snp	C/T	1.65419e-05	0.00287588	missense, utr-variant-5-prime	MED16	GRCh38.p7	19:891055	GGGCAGTGGGTGCTC[C/T]TGGACCATTTCTCCC	10025
rs760620315	in-del	-/AG	4.42204e-05	0.00470194	intron-variant	MED16	GRCh38.p7	19:868375	GGGGCAGCTGGGCTC[-/AG]GGGTAGCTGAGGGGC	10025
rs760648552	snp	A/G	1.75314e-05	0.00296064	intron-variant	MED16	GRCh38.p7	19:886224	GAAGGGAGGGAGGGA[A/G]GAGGGGCCGCTCAGG	10025
rs760654263	snp	C/T			intron-variant	MED16	GRCh38.p7	19:870435	GTGTGGTGGCTCATG[C/T]CTGTAATCCCAGCTA	10025
rs760656271	snp	A/G	1.97771e-05	0.00314455	missense	MED16	GRCh38.p7	19:871946	ATCCAGAGCTTGGTG[A/G]GCAGGCGGAAGAGCA	10025
rs760683174	snp	C/T			intron-variant	MED16	GRCh38.p7	19:882133	TCGCACCCACAGATC[C/T]GCTGCCTGACAGCCC	10025
rs760702768	snp	C/T	2.41316e-05	0.0034735	missense	MED16	GRCh38.p7	19:868190	CCAGCTGGACAAAGG[C/T]AGGGGCTTCCTCAGA	10025
rs760712095	snp	C/G	0.000257535	0.0113447	intron-variant	MED16	GRCh38.p7	19:881730	CTGAAAAATCAGGGG[C/G]AGGAAAACAGGAAGG	10025
rs760738341	snp	A/G			intron-variant	MED16	GRCh38.p7	19:889945	CAGGTGGCACAAGGC[A/G]CACTCCAGAGATGCC	10025
rs760748257	snp	G/T	1.92384e-05	0.00310142	synonymous-codon	MED16	GRCh38.p7	19:880096	GGCCATGGTCTGCAG[G/T]GAGAGCCGGTGCACG	10025
rs760780818	snp	A/G			intron-variant	MED16	GRCh38.p7	19:874361	TCGTGATCAGCCCGC[A/G]TTGGCCTCCCAAAGT	10025
rs760813983	snp	A/C	1.77843e-05	0.00298191	intron-variant	MED16	GRCh38.p7	19:889619	CTGCCTCATCCGCTC[A/C]CTCGGGCAGGACACT	10025
rs760818693	snp	A/T			intron-variant	MED16	GRCh38.p7	19:874848	GTGCTGCAACCTGGA[A/T]GACACAGTGAGACCG	10025
rs760892238	snp	C/T	0.000163261	0.00903348	intron-variant	MED16	GRCh38.p7	19:885039	GGGTGAGGGCTGACC[C/T]GGCACTGCTGTGGTG	10025
rs760893703	snp	A/C/G	0.000200132	0.0100015	intron-variant	MED16	GRCh38.p7	19:872124	GCAGGGAACCCTGCC[A/C/G]GAAAGAGGCATCGGT	10025
rs760915188	snp	A/G	1.69983e-05	0.00291528	missense, intron-variant	MED16	GRCh38.p7	19:877035	TCCACCAGGCTCTGT[A/G]CCATACTGGGCTGCA	10025
rs760916612	in-del	-/GAG	3.36434e-05	0.00410129	intron-variant	MED16	GRCh38.p7	19:868285	TAACCGCGCCGAGGA[-/GAG]GAGTCCAGGGCGAGC	10025
rs760944826	snp	G/T	2.0129e-05	0.0031724	intron-variant	MED16	GRCh38.p7	19:872149	ATCGGTGTGGCTGGG[G/T]CGGCGGGGGGCAGAT	10025
rs760947051	snp	A/G	5.63322e-05	0.00530688	intron-variant	MED16	GRCh38.p7	19:871610	CAAACAGGTGCCTGG[A/G]AGTGGCTGCCATCCC	10025
rs760982903	snp	C/T			intron-variant	MED16	GRCh38.p7	19:884059	CGGGGCCTCTTGACA[C/T]GTGCTCATTAGTGGC	10025
rs761001973	snp	C/T	1.83038e-05	0.00302515	intron-variant	MED16	GRCh38.p7	19:890915	ACCTGGGGAACAGGG[C/T]GGGACACCATGCGGC	10025
rs761020417	snp	A/G	0.00010158	0.00712597	synonymous-codon	MED16	GRCh38.p7	19:886061	CGTCAGCACCTGCCC[A/G]CTGGGCTTCAGCAGG	10025
rs761038097	snp	C/T			intron-variant	MED16	GRCh38.p7	19:891479	GCAGCGGAGGGTCTG[C/T]GCTGGCCCAGGTGAG	10025
rs761069833	snp	G/T	1.7321e-05	0.00294282	intron-variant	MED16	GRCh38.p7	19:868542	TCCCACTTCCAGGCG[G/T]GCCTCCCTTACGCCT	10025
rs761072743	snp	A/G	1.79879e-05	0.00299894	missense, intron-variant	MED16	GRCh38.p7	19:877120	GGAAGAGCAGGTGCC[A/G]CAGCGCCAGCCCCAC	10025
rs761128908	snp	A/G	1.85948e-05	0.00304911	utr-variant-3-prime	MED16	GRCh38.p7	19:868064	CGAGGAGACGCCCGA[A/G]CCGGGTCACCACAAG	10025
rs761164484	snp	A/G			intron-variant	MED16	GRCh38.p7	19:890705	CTCCAACAAGCCTCC[A/G]TCAACCAACGCTCCA	10025
rs761169713	snp	A/G	3.93786e-05	0.00443709	synonymous-codon	MED16	GRCh38.p7	19:871168	TGGCAGCCAGTCCAG[A/G]CTGGGGATAAGCAGC	10025
rs761188050	snp	C/T			intron-variant	MED16	GRCh38.p7	19:869762	TTTTGCTCATCTGTG[C/T]TTTCTAAAATTCCAG	10025
rs761197468	snp	C/G	1.67239e-05	0.00289166	intron-variant	MED16	GRCh38.p7	19:873615	TCGGGTCAGCTCGGG[C/G]CTCTTGTACACACAG	10025
rs761282748	snp	A/G	1.72579e-05	0.00293746	intron-variant	MED16	GRCh38.p7	19:881740	AGGGGCAGGAAAACA[A/G]GAAGGCAATGGAGTA	10025
rs761326532	snp	G/T	1.68989e-05	0.00290674	missense	MED16	GRCh38.p7	19:872034	TCAGAAGGCCCCAGA[G/T]GCGGATGACCACCAT	10025
rs761329578	in-del	-/GGGCCCCACCTGCCACA	9.81008e-05	0.00700291	intron-variant	MED16	GRCh38.p7	19:876964	GCCCCACCTGCCACG[-/GGGCCCCACCTGCCACA]GGCCCCCACCTGCTG	10025
rs761398435	snp	A/C			intron-variant	MED16	GRCh38.p7	19:869246	AGGGTCGGTCCGCCA[A/C]GTGCCCGGGGAGCCT	10025
rs761406984	snp	C/T	4.57007e-05	0.00477999	intron-variant	MED16	GRCh38.p7	19:875506	AGCAGAGGCGCCCGC[C/T]AAGGCTCCAGCTGAG	10025
rs761411743	snp	C/T	0.000116257	0.0076233	missense, intron-variant	MED16	GRCh38.p7	19:889781	ACTTGATCTGCCCGT[C/T]GGCATCTGCTGACAG	10025
rs761429221	in-del	-/G	1.66668e-05	0.00288672	frameshift-variant	MED16	GRCh38.p7	19:885814	GAGGTGGGTGATGGC[-/G]GGGAAACTTGTCCTT	10025
rs761446668	snp	C/G/T	3.95196e-05	0.00444506	missense	MED16	GRCh38.p7	19:880001	TGCATAGCCTTTAAG[C/G/T]GGACGGCGGGGCCCG	10025
rs761460139	snp	A/C/G	3.49799e-05	0.00418198	intron-variant	MED16	GRCh38.p7	19:873422	GCCCAGGTGGGGGGC[A/C/G]GGGCCTTAGGGGAGA	10025
rs761493983	snp	C/T			intron-variant	MED16	GRCh38.p7	19:887395	AAATTTGGCCGGACG[C/T]GGTGGCTCACGCCTG	10025
rs761520853	snp	A/G	0.000404449	0.0142148	synonymous-codon	MED16	GRCh38.p7	19:871231	CGCCTCGTCCGGCTC[A/G]CTCGCTGGGCCCTCA	10025
rs761571390	snp	A/C	0.000210532	0.0102578	intron-variant	MED16	GRCh38.p7	19:889835	AGCCATCATTGCGAA[A/C]CTTCCAGGGATGGGC	10025
rs761571748	snp	A/G			intron-variant	MED16	GRCh38.p7	19:876155	TTTTTTTCCCATTTT[A/G]TCTTCGTATTGGTTT	10025
rs761658770	snp	A/G	2.08701e-05	0.00323026	intron-variant	MED16	GRCh38.p7	19:868381	GCTGGGCTCAGGGGT[A/G]GCTGAGGGGCACCCG	10025
rs761731274	snp	C/T	1.66327e-05	0.00288376	missense	MED16	GRCh38.p7	19:885841	CCTTGCGGTTGAGGT[C/T]GGTGGTGCAGCGCAT	10025
rs761757727	snp	C/T	3.35971e-05	0.00409846	missense, utr-variant-5-prime	MED16	GRCh38.p7	19:890971	GACGCACCCTGGTCA[C/T]CGCTGCGCAGGTCCA	10025
rs761759578	snp	A/G	1.68752e-05	0.00290471	intron-variant	MED16	GRCh38.p7	19:871911	AGAGGGGAGGGGCGG[A/G]CGGGGGTGCCTCACA	10025
rs761772596	snp	C/T	1.65468e-05	0.00287631	synonymous-codon, utr-variant-5-prime	MED16	GRCh38.p7	19:891039	GGCCAGGGGCACCGA[C/T]GGGCAGTGGGTGCTC	10025
rs761788284	snp	A/G	1.75696e-05	0.00296386	synonymous-codon	MED16	GRCh38.p7	19:868909	AAGCGCCAAGGTGCA[A/G]CCTCCGCAGGTGGTC	10025
rs761844567	snp	A/C	1.69997e-05	0.0029154	intron-variant	MED16	GRCh38.p7	19:879886	AGCAGCTCGCCTTCC[A/C]CTGGTTGTCAATGCC	10025
rs761849051	in-del	-/CCTTCAACAGC	3.16341e-05	0.00397694	frameshift-variant	MED16	GRCh38.p7	19:868240	GCGTCCGGCCCACGG[-/CCTTCAACAGC]CCTGCAGGGCGGGCT	10025
rs761852580	snp	A/G	8.82081e-05	0.0066405	intron-variant	MED16	GRCh38.p7	19:886221	GGAGAAGGGAGGGAG[A/G]GAGGAGGGGCCGCTC	10025
rs761909396	in-del	-/TTC			upstream-variant-2KB, downstream-variant-500B	MED16, RNU6-9	GRCh38.p7	19:893599	TATTTTTTTTTTTTT[-/TTC]CATTTTCCCTCCCAG	10025
rs761913910	snp	C/G/T	5.10646e-05	0.00505273	missense	MED16	GRCh38.p7	19:872088	AGGTGCCGTCCCGCA[C/G/T]AAAGCTGTGGCCCGG	10025
rs761925501	snp	A/G	6.1841e-05	0.00556028	missense, utr-variant-5-prime	MED16	GRCh38.p7	19:886149	CCGAACAGCGTGAGC[A/G]ACGGTGAGAACTTGA	10025
rs761947243	snp	C/T			intron-variant	MED16	GRCh38.p7	19:871537	TTCCAGACACTGGGA[C/T]GTAAGAATGACACAG	10025
rs762010412	snp	C/T			intron-variant	MED16	GRCh38.p7	19:888957	GAACATCCCCGAGAC[C/T]CTGCCGTCAGTGAGG	10025
rs762041536	snp	A/G	2.87253e-05	0.0037897	missense	MED16	GRCh38.p7	19:884999	TCTGGCTGGACGCGC[A/G]CAAAAGCACCTGCGG	10025
rs762043487	snp	A/C/G/T	0.000172645	0.00928972	synonymous-codon	MED16	GRCh38.p7	19:880063	CACAGGCCTCGGGGC[A/C/G/T]GCGGAGCTGTAGAAG	10025
rs762115607	snp	C/G			intron-variant	MED16	GRCh38.p7	19:874914	TTAGGCTATATCCCA[C/G]CACTTTAGGAGGCCG	10025
rs762119472	snp	A/G	3.60991e-05	0.00424832	intron-variant	MED16	GRCh38.p7	19:872121	TCAGCAGGGAACCCT[A/G]CCCGAAAGAGGCATC	10025
rs762208180	in-del	-/CCACA	2.54101e-05	0.00356432	intron-variant	MED16	GRCh38.p7	19:876925	CGGGGCCCCCACCTG[-/CCACA]GGGCCCCCACCTGCC	10025
rs762212133	snp	A/G	6.7996e-05	0.00583038	stop-gained, intron-variant	MED16	GRCh38.p7	19:877033	TCTCCACCAGGCTCT[A/G]TACCATACTGGGCTG	10025
rs762224687	snp	A/G			intron-variant	MED16	GRCh38.p7	19:884142	CCAGGGTCCATTAGC[A/G]CTAATCGGCAAATGC	10025
rs762259405	snp	A/G	3.33734e-05	0.0040848	synonymous-codon	MED16	GRCh38.p7	19:873533	CTGCAGTGTGTTCAT[A/G]TCCAGCACAAATTCC	10025
rs762275550	snp	A/G	1.69919e-05	0.00291473	intron-variant	MED16	GRCh38.p7	19:868509	CCGCACCTGCGGGGA[A/G]GCAGGCACTGAGCGG	10025
rs762295392	snp	A/G	0.000202761	0.0100667	missense	MED16	GRCh38.p7	19:868458	CACTGCTTCACCGCC[A/G]TGGTTCTGTTGGGCG	10025
rs762378756	snp	C/T			upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:893482	GGTGGAACTCAATAT[C/T]CGTGCTCGCTTCGGC	10025
rs762452494	in-del	-/CAT	1.6896e-05	0.0029065	cds-indel	MED16	GRCh38.p7	19:872047	GATGCGGATGACCAC[-/CAT]CAATTCCCGAAGCAT	10025
rs762452886	snp	A/G	6.67902e-05	0.00577846	missense, utr-variant-5-prime	MED16	GRCh38.p7	19:891116	CACCTGCCGCTGGCC[A/G]CCGCAAATCACACAT	10025
rs762470700	snp	A/G	1.66866e-05	0.00288842	intron-variant	MED16	GRCh38.p7	19:873589	TGTCAATGTCTACAA[A/G]GAGACGTGGGTCGGG	10025
rs762481861	in-del	-/TG	0.000237259	0.0108891	frameshift-variant, intron-variant	MED16	GRCh38.p7	19:876978	CGGGCCCCCACCTGC[-/TG]CAGGGCAGCGGTCTG	10025
rs762485115	in-del	-/A			intron-variant	MED16	GRCh38.p7	19:881725	GCCAACTGAAAAATC[-/A]GGGGCAGGAAAACAG	10025
rs762494867	snp	A/G	7.23484e-05	0.00601407	missense	MED16	GRCh38.p7	19:871959	TGAGCAGGCGGAAGA[A/G]CAGGGACATGCTGTC	10025
rs762527337	snp	A/G	5.39331e-05	0.00519265	synonymous-codon	MED16	GRCh38.p7	19:885995	GCCGCCGGTGAAGGC[A/G]ATGTCGGCCAGGGCC	10025
rs762543168	snp	C/T	1.97701e-05	0.00314399	missense	MED16	GRCh38.p7	19:879993	ACGATAGCTGCATAG[C/T]CTTTAAGTGGACGGC	10025
rs762616606	snp	C/T	3.30863e-05	0.00406719	intron-variant	MED16	GRCh38.p7	19:868260	AACAGCCCTGCAGGG[C/T]GGGCTGAGGTTAACC	10025
rs762618349	in-del	-/CAC	7.40316e-05	0.00608361	cds-indel	MED16	GRCh38.p7	19:868071	ACGCCCGAGCCGGGT[-/CAC]CACAAGGTCCGCCTG	10025
rs762636286	snp	C/T			intron-variant	MED16	GRCh38.p7	19:869894	CGGCCACTTCCTGAC[C/T]GCGTGACCCCAGATG	10025
rs762694444	snp	A/G	0.000135035	0.00821579	missense	MED16	GRCh38.p7	19:871110	CAAACTGCAGACGAA[A/G]GGGCTGCTTGGGCTG	10025
rs762694539	snp	C/G	1.70554e-05	0.00292017	missense	MED16	GRCh38.p7	19:871988	TCCTGGGTATCCGAG[C/G]TGGCCGTATACACGG	10025
rs762705965	snp	G/T			intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:892525	GAGGCTTCATCCCAG[G/T]GACCCCATAGCCTCT	10025
rs762750210	snp	A/G			intron-variant	MED16	GRCh38.p7	19:887845	CAACTGGGTCTCGGG[A/G]GCTGGGGTGGGGGAT	10025
rs762856187	in-del	-/CACACT			intron-variant	MED16	GRCh38.p7	19:886592	CTGGTGCCAATGAGC[-/CACACT]CACAAACCCAGGCGG	10025
rs762884165	snp	C/T	3.4013e-05	0.00412376	intron-variant	MED16	GRCh38.p7	19:885763	GTGATGGCCTGCGCC[C/T]GTTCACCTGCTCCGA	10025
rs762904040	snp	G/T	5.31986e-05	0.00515718	intron-variant	MED16	GRCh38.p7	19:873415	GATGGGGGCCCAGGT[G/T]GGGGGCGGGGCCTTA	10025
rs762917828	snp	A/G	2.12927e-05	0.0032628	synonymous-codon	MED16	GRCh38.p7	19:880135	GCTGCCGTCGTGGAA[A/G]GCCAGGGCCAGCCCT	10025
rs762918725	in-del	-/CCT			intron-variant	MED16	GRCh38.p7	19:881383	GAAAGATGAGATCTG[-/CCT]CCTAATTGGGAACCC	10025
rs763007553	snp	A/G	8.47877e-05	0.0065105	intron-variant	MED16	GRCh38.p7	19:880183	CTTAGACATGGGCAG[A/G]GCCCAGGACACGCCC	10025
rs763063011	snp	A/G	5.33063e-05	0.0051624	intron-variant	MED16	GRCh38.p7	19:875219	GAAAGAAACCTCGAG[A/G]CCCCGGGCGTGGAAA	10025
rs763073436	snp	A/G	3.53076e-05	0.0042015	missense	MED16	GRCh38.p7	19:868896	TCCTCCGTGGGGCAA[A/G]CGCCAAGGTGCAGCC	10025
rs763076728	snp	A/C/G	3.75622e-05	0.00433355	missense	MED16	GRCh38.p7	19:871238	TCCGGCTCGCTCGCT[A/C/G]GGCCCTCATCGCGAC	10025
rs763082280	snp	A/G			intron-variant	MED16	GRCh38.p7	19:870681	TAGGGGCACCTAGAA[A/G]GAAGCAGCAGTCATG	10025
rs763108511	snp	A/G			intron-variant	MED16	GRCh38.p7	19:890583	TTCTCTAATGACCAC[A/G]TATTATGAGTGCCTA	10025
rs763125423	snp	A/G	4.10905e-05	0.0045325	missense, utr-variant-5-prime	MED16	GRCh38.p7	19:886143	TTGCCGCCGAACAGC[A/G]TGAGCGACGGTGAGA	10025
rs763141504	snp	A/T			intron-variant	MED16	GRCh38.p7	19:868728	CACATCCTGGGATCC[A/T]GGCTCCAACACTCCC	10025
rs763166625	snp	A/G	9.1343e-05	0.00675745	missense, intron-variant	MED16	GRCh38.p7	19:877168	TGGAAGGTGAGAGGC[A/G]GAGCACGCTCAGCTG	10025
rs763168493	in-del	-/TT	3.33689e-05	0.00408453	frameshift-variant	MED16	GRCh38.p7	19:875294	CGGTCGCCGGGGCTC[-/TT]GTCAGGCGTGTTGAG	10025
rs763253661	snp	A/C/G	0.000290313	0.0120448	intron-variant	MED16	GRCh38.p7	19:877204	GACAGAGCCCAAGGA[A/C/G]AGCCCGGTGAGATGG	10025
rs763268262	snp	C/T	5.04706e-05	0.00502322	missense	MED16	GRCh38.p7	19:875264	TCGGTGATCTTGGTG[C/T]AGATCTCGGTCAGCC	10025
rs763281890	snp	C/T	4.41647e-05	0.00469898	intron-variant	MED16	GRCh38.p7	19:884888	CAGGGCCTCCGCAGC[C/T]GGCGGGAGACTCACC	10025
rs763320666	snp	C/G/T	3.39854e-05	0.00412211	missense	MED16	GRCh38.p7	19:872084	AGCGAGGTGCCGTCC[C/G/T]GCAGAAAGCTGTGGC	10025
rs763320958	snp	A/T	0.00012463	0.007893	intron-variant	MED16	GRCh38.p7	19:889851	CTTCCAGGGATGGGC[A/T]GAGCACTGCGTTGCA	10025
rs763360343	snp	A/G/T	3.78481e-05	0.00435005	missense	MED16	GRCh38.p7	19:868142	GGTCCAGGGATCTGG[A/G/T]GGTCCTGGGAGAGTG	10025
rs763364062	snp	C/T			intron-variant	MED16	GRCh38.p7	19:875118	GCAGTGAGCTGAGAT[C/T]GCACCACTGCACTCC	10025
rs763366122	snp	A/G	1.76789e-05	0.00297307	synonymous-codon	MED16	GRCh38.p7	19:872112	GGCCCGGCCTCAGCA[A/G]GGAACCCTGCCCGAA	10025
rs763377555	snp	A/T	2.37764e-05	0.00344785	missense	MED16	GRCh38.p7	19:884926	GAGATCTGCTGGAAG[A/T]TGTTGTTCACGGGGA	10025
rs763384102	in-del	-/A			intron-variant	MED16	GRCh38.p7	19:888526	GAGACTCTGTCTCCA[-/A]AAAAAAAAAAAAAAA	10025
rs763402654	snp	C/G	8.99936e-05	0.00670736	missense, intron-variant	MED16	GRCh38.p7	19:876982	CCCCCACCTGCTGCA[C/G]GGCAGCGGTCTGGCG	10025
rs763410910	snp	C/T			intron-variant	MED16	GRCh38.p7	19:885197	ATCCACTCACAGGAA[C/T]GCAAATGTCCCCGGA	10025
rs763429943	in-del	-/C			intron-variant	MED16	GRCh38.p7	19:868677	CCCAGCAATGCTGCT[-/C]CCTGAACTAGCCCCG	10025
rs763443346	snp	C/G	1.94979e-05	0.00312227	missense	MED16	GRCh38.p7	19:880026	GGCCCGCGGTGCGGG[C/G]GCGCTTCATGGCCGG	10025
rs763448493	snp	A/G	3.91596e-05	0.00442474	intron-variant	MED16	GRCh38.p7	19:871567	GCTCACCCTCCTCAC[A/G]TACACACAACCCGAC	10025
rs763497108	snp	A/G	1.67089e-05	0.00289035	missense	MED16	GRCh38.p7	19:881672	AGATCGTTGGTGGCC[A/G]ATAGGATCCGCCATT	10025
rs763502675	snp	A/G			intron-variant	MED16	GRCh38.p7	19:885676	ACCACGGTTTAGCCC[A/G]TGGAGGCCCGCGCGG	10025
rs763503689	snp	A/G	3.83384e-05	0.0043781	intron-variant	MED16	GRCh38.p7	19:868396	AGCTGAGGGGCACCC[A/G]CCACCAGAGCCCACC	10025
rs763517096	in-del	-/C			intron-variant	MED16	GRCh38.p7	19:884857	AATAAAAACCAACCG[-/C]CCCCGAGGGCAGGCC	10025
rs763556066	snp	A/T	1.70502e-05	0.00291972	missense	MED16	GRCh38.p7	19:871989	CCTGGGTATCCGAGG[A/T]GGCCGTATACACGGG	10025
rs763593432	snp	A/G			upstream-variant-2KB	MED16	GRCh38.p7	19:894225	ATTTTTAGTAGAGAC[A/G]GAGTTTCACCATGTT	10025
rs763610157	snp	C/G			intron-variant	MED16	GRCh38.p7	19:876396	GACCGTGTTTGCTGA[C/G]GCCTCACACCACAGG	10025
rs763634772	snp	C/T	3.4379e-05	0.00414588	intron-variant	MED16	GRCh38.p7	19:889635	CTCGGGCAGGACACT[C/T]ACCTTCTCCACGTGC	10025
rs763651537	snp	A/C/T	7.20557e-05	0.00600195	synonymous-codon	MED16	GRCh38.p7	19:871960	GAGCAGGCGGAAGAG[A/C/T]AGGGACATGCTGTCC	10025
rs763671251	snp	A/G			intron-variant	MED16	GRCh38.p7	19:868854	TCAGCGGTTCCGGGG[A/G]CCCCTCACCTGGTGC	10025
rs763709655	snp	A/C/G/T	6.85538e-05	0.00585434	intron-variant	MED16	GRCh38.p7	19:891154	GTCACCAGCTCCTGC[A/C/G/T]GGAGGGAGGTGTGGT	10025
rs763751968	snp	A/C	1.97428e-05	0.00314181	missense	MED16	GRCh38.p7	19:879999	GCTGCATAGCCTTTA[A/C]GTGGACGGCGGGGCC	10025
rs763762136	in-del	-/CG	7.26427e-05	0.00602628	frameshift-variant, intron-variant	MED16	GRCh38.p7	19:876981	CCCCCACCTGCTGCA[-/CG]GGGCAGCGGTCTGGC	10025
rs763793613	snp	C/T	2.04205e-05	0.00319528	stop-gained	MED16	GRCh38.p7	19:871159	GTCGCTGGCTGGCAG[C/T]CAGTCCAGGCTGGGG	10025
rs763823978	snp	A/G			intron-variant	MED16	GRCh38.p7	19:886461	GAACGTGTGCGCAAC[A/G]GGAGTCACCTCCCCT	10025
rs763830916	snp	A/G			intron-variant	MED16	GRCh38.p7	19:872857	AAGGAGCAGGGCCTG[A/G]GAGGCGGGGCTTTGA	10025
rs763849618	snp	G/T			intron-variant	MED16	GRCh38.p7	19:874468	ACGCCTGTAATCCCA[G/T]CGCTTTGGGAGGCAG	10025
rs763874862	snp	G/T	2.07278e-05	0.00321923	intron-variant	MED16	GRCh38.p7	19:872157	GGCTGGGGCGGCGGG[G/T]GGCAGATGGCGATGG	10025
rs763877714	snp	C/T	1.71466e-05	0.00292797	synonymous-codon, intron-variant	MED16	GRCh38.p7	19:889704	CACAATGGGGTCCCC[C/T]TCCACTAGGCTGCCC	10025
rs763947153	snp	A/G	4.58642e-05	0.00478853	intron-variant	MED16	GRCh38.p7	19:875464	GAGGACCTGAGGGCA[A/G]GAAGCCAGGTCACCC	10025
rs763977027	snp	A/G			upstream-variant-2KB	MED16	GRCh38.p7	19:894533	TACAGGTTAACAATG[A/G]CCCAAATATCAGAGT	10025
rs764014813	snp	A/T	4.29304e-05	0.00463286	missense	MED16	GRCh38.p7	19:880139	CCGTCGTGGAAGGCC[A/T]GGGCCAGCCCTGTGG	10025
rs764032629	snp	A/C/G	3.82931e-05	0.00437554	intron-variant	MED16	GRCh38.p7	19:871692	GATATCAAGGCAGAG[A/C/G]CACTGCCACCTGCAG	10025
rs764097799	snp	C/T	1.98639e-05	0.00315144	missense	MED16	GRCh38.p7	19:886099	TGACCAGGCCGCTGA[C/T]CGTCACCGCGATCCA	10025
rs764164815	snp	C/T	1.68735e-05	0.00290456	missense, utr-variant-5-prime	MED16	GRCh38.p7	19:890965	GAGGGGGACGCACCC[C/T]GGTCATCGCTGCGCA	10025
rs764174508	snp	A/G/T	6.88871e-05	0.00586846	intron-variant	MED16	GRCh38.p7	19:880189	CATGGGCAGGGCCCA[A/G/T]GACACGCCCGCCGGG	10025
rs764256954	snp	C/T	1.77439e-05	0.00297853	intron-variant	MED16	GRCh38.p7	19:875220	AAAGAAACCTCGAGG[C/T]CCCGGGCGTGGAAAA	10025
rs764264522	snp	A/G	4.59971e-05	0.00479546	synonymous-codon, intron-variant	MED16	GRCh38.p7	19:877169	GGAAGGTGAGAGGCG[A/G]AGCACGCTCAGCTGC	10025
rs764311882	snp	C/G	1.68929e-05	0.00290623	missense	MED16	GRCh38.p7	19:872050	GCGGATGACCACCAT[C/G]AATTCCCGAAGCATG	10025
rs764327154	in-del	-/AAGC			intron-variant	MED16	GRCh38.p7	19:887233	GTCCAGAAGTCCAGG[-/AAGC]AAGCCAGGCCTGGTG	10025
rs764334049	snp	A/G	3.67701e-05	0.00428762	utr-variant-3-prime	MED16	GRCh38.p7	19:868080	CCGGGTCACCACAAG[A/G]TCCGCCTGGACCCCC	10025
rs764341441	snp	A/G	8.56568e-05	0.00654378	intron-variant	MED16	GRCh38.p7	19:884889	AGGGCCTCCGCAGCC[A/G]GCGGGAGACTCACCC	10025
rs764354653	snp	A/C	3.59454e-05	0.00423927	synonymous-codon	MED16	GRCh38.p7	19:868107	CCCCGGCCGTCACGG[A/C]CGGTCCTCTGGATGC	10025
rs764355331	snp	A/G	3.89681e-05	0.0044139	synonymous-codon	MED16	GRCh38.p7	19:880027	GCCCGCGGTGCGGGG[A/G]CGCTTCATGGCCGGC	10025
rs764396367	snp	C/T	0.000128233	0.00800624	intron-variant	MED16	GRCh38.p7	19:876951	CCACCTGCCACGGGG[C/T]CCCACCTGCCACGGG	10025
rs764405770	snp	C/G			upstream-variant-2KB	MED16	GRCh38.p7	19:895063	TGCACTCCAGCCTGG[C/G]GGACAGAGCAAGACT	10025
rs764407013	snp	A/G			intron-variant	MED16	GRCh38.p7	19:884060	GGGGCCTCTTGACAC[A/G]TGCTCATTAGTGGCT	10025
rs764431530	snp	A/G	2.3711e-05	0.0034431	synonymous-codon	MED16	GRCh38.p7	19:884928	GATCTGCTGGAAGAT[A/G]TTGTTCACGGGGAGT	10025
rs764524747	snp	G/T	0.00017265	0.00928953	missense	MED16	GRCh38.p7	19:880061	TCCACAGGCCTCGGG[G/T]CCGCGGAGCTGTAGA	10025
rs764534748	in-del	-/GGGGAGAGGGGA/GGGGAGCGGGGA	0.000149112	0.0086335	intron-variant	MED16	GRCh38.p7	19:871915	GGAGGGGCGGGCGGG[-/GGGGAGAGGGGA/GGGGAGCGGGGA]GGTGCCTCACAGCAG	10025
rs764539710	snp	A/C	1.903e-05	0.00308458	intron-variant	MED16	GRCh38.p7	19:868397	GCTGAGGGGCACCCG[A/C]CACCAGAGCCCACCG	10025
rs764612619	snp	G/T	3.59144e-05	0.00423744	synonymous-codon, intron-variant	MED16	GRCh38.p7	19:876983	CCCCACCTGCTGCAG[G/T]GCAGCGGTCTGGCGC	10025
rs764685792	snp	A/G	5.01479e-05	0.00500714	synonymous-codon	MED16	GRCh38.p7	19:881605	CACCTTGAGGTCGGT[A/G]TTGGTGAGCGAGATG	10025
rs764750486	snp	A/G	3.47084e-05	0.00416569	intron-variant	MED16	GRCh38.p7	19:881547	GCGTGGCTGCCGCTG[A/G]CTCCACCGTACCGAG	10025
rs764767247	snp	C/G	9.62881e-05	0.00693792	synonymous-codon, utr-variant-5-prime	MED16	GRCh38.p7	19:890189	GTGCTCTGAGGGGAT[C/G]GAGTGCAGGTCCCAG	10025
rs764824606	in-del	-/C	3.87135e-05	0.00439946	intron-variant	MED16	GRCh38.p7	19:876967	CCCACCTGCCACGGG[-/C]CCCCACCTGCTGCAG	10025
rs764827437	snp	A/G			intron-variant	MED16	GRCh38.p7	19:869827	TGCTCCTTGTCAAAC[A/G]TGTGTCTGAAACAGG	10025
rs764834681	snp	A/G	1.68388e-05	0.00290158	synonymous-codon	MED16	GRCh38.p7	19:873473	TAGGCTGGCCAGCAG[A/G]TACAGCACGAAGTCG	10025
rs764840974	in-del	-/GGCCCCCACCTGCCACAT	2.83901e-05	0.00376753	intron-variant	MED16	GRCh38.p7	19:876930	CCCCACCTGCCACAG[-/GGCCCCCACCTGCCACAT]GGCCCCCACCTGCCA	10025
rs764889815	snp	C/G/T	3.33941e-05	0.00408609	synonymous-codon	MED16	GRCh38.p7	19:873524	CTGCAGCGCCTGCAG[C/G/T]GTGTTCATGTCCAGC	10025
rs764891821	snp	G/T	0.000547959	0.0165433	intron-variant	MED16	GRCh38.p7	19:871918	AGGGGCGGGCGGGGG[G/T]GCCTCACAGCAGATC	10025
rs764958390	snp	C/T	9.05893e-05	0.00672952	missense	MED16	GRCh38.p7	19:871106	CGGCCAAACTGCAGA[C/T]GAAGGGGCTGCTTGG	10025
rs764983687	snp	A/G			intron-variant	MED16	GRCh38.p7	19:890311	ATGACGATGACTCCA[A/G]GCAGGCTCCAGGTAA	10025
rs764984479	snp	A/G	1.66704e-05	0.00288703	synonymous-codon	MED16	GRCh38.p7	19:875341	CAGCGACTTCAGGGT[A/G]GAGCTGATGGCGATG	10025
rs764994870	snp	A/C			intron-variant	MED16	GRCh38.p7	19:887404	CGGACGCGGTGGCTC[A/C]CGCCTGTAATCTCAG	10025
rs765012844	snp	A/C/T	0.000149698	0.00865038	missense	MED16	GRCh38.p7	19:879942	AGCAGCTCACCTTCC[A/C/T]GTGGCTGTCAATCCC	10025
rs765037683	snp	C/G/T	5.01662e-05	0.0050081	missense	MED16	GRCh38.p7	19:875385	TGTGGTAGTCGCACA[C/G/T]GCGGGTCACCGTGCA	10025
rs765048928	snp	A/G			intron-variant	MED16	GRCh38.p7	19:876443	CCTGGTACCCATCAC[A/G]TTCTGAGAGGATGGC	10025
rs765102154	snp	A/C	3.65037e-05	0.00427206	intron-variant	MED16	GRCh38.p7	19:872126	AGGGAACCCTGCCCG[A/C]AAGAGGCATCGGTGT	10025
rs765147373	snp	C/G/T	7.24329e-05	0.00601766	intron-variant	MED16	GRCh38.p7	19:885017	AAAGCACCTGCGGGG[C/G/T]AGGTGGGGGTGAGGG	10025
rs765189274	snp	A/G			intron-variant	MED16	GRCh38.p7	19:870114	TCCTCCTGATGAGGT[A/G]TCTGCTCAGCAGGGC	10025
rs765198629	in-del	-/GCCCC			intron-variant	MED16	GRCh38.p7	19:878247	CCAGCCCCAGCCCCA[-/GCCCC]AGCCCCACGGGCCCC	10025
rs765233859	snp	C/T	0.00030567	0.0123589	intron-variant	MED16	GRCh38.p7	19:890366	AGGTCACAGAACTGC[C/T]GTCAGCCGAGTCGAC	10025
rs765286348	in-del	-/G			intron-variant	MED16	GRCh38.p7	19:880535	GCTGTCACTCACACT[-/G]GGGGTCTGCCATTGT	10025
rs765310726	snp	A/G	5.82349e-05	0.00539574	missense	MED16	GRCh38.p7	19:880104	TCTGCAGTGAGAGCC[A/G]GTGCACGATGTGGAC	10025
rs765365602	snp	C/T	3.73692e-05	0.00432241	synonymous-codon, intron-variant	MED16	GRCh38.p7	19:877136	CAGCGCCAGCCCCAC[C/T]TCCAGCGGGTGGCCC	10025
rs765379797	snp	A/G	1.96759e-05	0.00313649	synonymous-codon	MED16	GRCh38.p7	19:886016	GGCCAGGGCCACGCG[A/G]CCGCGCAGCCGGCAC	10025
rs765400605	snp	A/G	1.87929e-05	0.00306531	intron-variant	MED16	GRCh38.p7	19:871665	CCTGTGCTAGGAACT[A/G]GGGAAATAGCAGATA	10025
rs765430593	in-del	-/G			intron-variant	MED16	GRCh38.p7	19:891269	AACAGCCGATGCAAA[-/G]GCCCGGAGGCCAGAC	10025
rs765465634	snp	C/T	1.73507e-05	0.00294535	intron-variant	MED16	GRCh38.p7	19:881749	AAAACAGGAAGGCAA[C/T]GGAGTAAAGACAGGC	10025
rs765513401	snp	G/T	1.94975e-05	0.00312224	intron-variant	MED16	GRCh38.p7	19:875201	AAAATAAAATAAATA[G/T]ATGAAAGAAACCTCG	10025
rs765518061	snp	C/G			intron-variant	MED16	GRCh38.p7	19:889017	GCCTGAACCCAGGTG[C/G]CCCCCCAACCCTGGC	10025
rs765556744	snp	A/C	1.84099e-05	0.00303391	utr-variant-3-prime	MED16	GRCh38.p7	19:868077	GAGCCGGGTCACCAC[A/C]AGGTCCGCCTGGACC	10025
rs765571659	in-del	-/C	0.000194757	0.00986614	intron-variant	MED16	GRCh38.p7	19:871576	CTCACATACACACAA[-/C]CCCGACAAGGAGAGA	10025
rs765614101	snp	C/T			intron-variant	MED16	GRCh38.p7	19:885106	GGGGCCACGCACTGC[C/T]GGGCCTGTCTCTTCA	10025
rs765638851	snp	A/G	3.38003e-05	0.00411084	missense	MED16	GRCh38.p7	19:872037	GAAGGCCCCAGATGC[A/G]GATGACCACCATCAA	10025
rs765668765	snp	A/G	4.6031e-05	0.00479723	intron-variant	MED16	GRCh38.p7	19:884886	CCCAGGGCCTCCGCA[A/G]CCGGCGGGAGACTCA	10025
rs765689976	snp	A/G			intron-variant	MED16	GRCh38.p7	19:874637	TCTCAGCCCCCAGGA[A/G]TAGAGAGAGGTGAAA	10025
rs765743419	snp	C/T	7.91891e-05	0.00629192	intron-variant	MED16	GRCh38.p7	19:871558	AATGACACAGCTCAC[C/T]CTCCTCACATACACA	10025
rs765783244	snp	A/G	2.42674e-05	0.00348326	intron-variant	MED16	GRCh38.p7	19:868327	CAGCAGCCGGGCTCA[A/G]GGGCAGCTGAGGGGT	10025
rs765797831	in-del	-/AGAGGCATC	3.66703e-05	0.0042818	intron-variant	MED16	GRCh38.p7	19:872127	GGAACCCTGCCCGAA[-/AGAGGCATC]AGAGGCATCGGTGTG	10025
rs765838483	snp	A/G	2.10267e-05	0.00324236	missense, intron-variant	MED16	GRCh38.p7	19:889795	TCGGCATCTGCTGAC[A/G]GGAGCCGGGAGCCTG	10025
rs765867602	snp	C/G	2.00624e-05	0.00316714	intron-variant	MED16	GRCh38.p7	19:868390	AGGGGTAGCTGAGGG[C/G]CACCCGCCACCAGAG	10025
rs765879903	snp	C/T	5.81514e-05	0.00539187	intron-variant	MED16	GRCh38.p7	19:871702	CAGAGCCACTGCCAC[C/T]TGCAGGGGCTTATGT	10025
rs765903314	snp	A/G	1.66421e-05	0.00288458	missense	MED16	GRCh38.p7	19:885855	TCGGTGGTGCAGCGC[A/G]TGAACAGGGAGGGCA	10025
rs765953766	snp	A/G	2.21639e-05	0.00332888	intron-variant	MED16	GRCh38.p7	19:876945	GGGCCCCCACCTGCC[A/G]CGGGGCCCCACCTGC	10025
rs765965865	snp	A/G			intron-variant	MED16	GRCh38.p7	19:885376	CTCAGCCCTAGGACC[A/G]GTGGCTGGGCCGCCT	10025
rs765967429	snp	C/T			intron-variant	MED16	GRCh38.p7	19:888160	AGTGAGCCGAGATCG[C/T]GCCACTACACTCCAG	10025
rs766006755	snp	A/G	3.44679e-05	0.00415124	intron-variant	MED16	GRCh38.p7	19:873431	GGGGGCGGGGCCTTA[A/G]GGGAGAGCATGGCGC	10025
rs766087359	snp	A/C			intron-variant	MED16	GRCh38.p7	19:869904	CTGACCGCGTGACCC[A/C]AGATGAGTGGGGTGA	10025
rs766087841	snp	A/T			upstream-variant-2KB, nc-transcript-variant	MED16, RNU6-9	GRCh38.p7	19:893587	TGAAGCGTTCCATAT[A/T]TTTTTTTTTTTTTCC	10025
rs766096283	snp	A/G	0.000274657	0.0117155	intron-variant	MED16	GRCh38.p7	19:879890	GCTCGCCTTCCCCTG[A/G]TTGTCAATGCCCACC	10025
rs766116128	in-del	-/CACT			intron-variant	MED16	GRCh38.p7	19:884715	TCTATACGCCTAACA[-/CACT]CAGAATGCTGGCAGG	10025
rs766142218	snp	C/T			intron-variant	MED16	GRCh38.p7	19:869353	CTCTGCCCAGACACC[C/T]GGCCTGGAGGTGCCG	10025
rs766148301	snp	C/T	1.75906e-05	0.00296564	missense	MED16	GRCh38.p7	19:868923	AGCCTCCGCAGGTGG[C/T]CGATCTTGGGCTGGC	10025
rs766152476	snp	C/G	1.67421e-05	0.00289323	missense	MED16	GRCh38.p7	19:881593	TGTGTCGCTGGCCAC[C/G]TTGAGGTCGGTGTTG	10025
rs766179200	snp	G/T	4.70356e-05	0.00484929	intron-variant	MED16	GRCh38.p7	19:871916	GGAGGGGCGGGCGGG[G/T]GTGCCTCACAGCAGA	10025
rs766195021	snp	A/G	0.000233302	0.010798	synonymous-codon, utr-variant-5-prime	MED16	GRCh38.p7	19:890982	GTCATCGCTGCGCAG[A/G]TCCATGGTGAAGGCG	10025
rs766211411	snp	C/T	3.30797e-05	0.00406679	stop-gained, utr-variant-5-prime	MED16	GRCh38.p7	19:891069	CTTGGACCATTTCTC[C/T]CACTCACAGACGTAG	10025
rs766224197	snp	A/C/T	0.000117104	0.0076511	missense	MED16	GRCh38.p7	19:875283	TCTCGGTCAGCCGGT[A/C/T]GCCGGGGCTCTTGTC	10025
rs766251299	in-del	-/AGGG	0.000863732	0.0207634	intron-variant	MED16	GRCh38.p7	19:886210	GCCCGACTGTGGAGA[-/AGGG]AGGGAGGGAGGGAGG	10025
rs766289298	snp	C/G			intron-variant	MED16	GRCh38.p7	19:888056	AAAAATACAAAAAAG[C/G]AGCCGGGCGTGGTGG	10025
rs766304420	snp	C/T	0.00012845	0.00801304	synonymous-codon	MED16	GRCh38.p7	19:868200	AAAGGCAGGGGCTTC[C/T]TCAGAAGCTCTGCTG	10025
rs766347716	snp	C/T			intron-variant	MED16	GRCh38.p7	19:882906	GTGAGCAGCATTCCC[C/T]GGGGGGAAACAGGCC	10025
rs766481695	snp	A/G/T	7.69932e-05	0.00620415	synonymous-codon	MED16	GRCh38.p7	19:880099	CATGGTCTGCAGTGA[A/G/T]AGCCGGTGCACGATG	10025
rs766491748	in-del	-/A			intron-variant	MED16	GRCh38.p7	19:868375	GGGGCAGCTGGGCTC[-/A]GGGGTAGCTGAGGGG	10025
rs766519077	snp	C/G			intron-variant	MED16	GRCh38.p7	19:868268	TGCAGGGCGGGCTGA[C/G]GTTAACCGCGCCGAG	10025
rs766520142	snp	C/G	1.70603e-05	0.0029206	intron-variant	MED16	GRCh38.p7	19:868519	GGGGAGGCAGGCACT[C/G]AGCGGGTTCCCACTT	10025
rs766535778	snp	C/T	1.69887e-05	0.00291446	missense, intron-variant	MED16	GRCh38.p7	19:877039	CCAGGCTCTGTACCA[C/T]ACTGGGCTGCACGTG	10025
rs766593621	snp	A/G	1.91907e-05	0.00309758	missense	MED16	GRCh38.p7	19:886011	ATGTCGGCCAGGGCC[A/G]CGCGGCCGCGCAGCC	10025
rs766628949	snp	C/T			intron-variant	MED16	GRCh38.p7	19:890129	GCCACGTGGGACCAG[C/T]GCCTCACCTGACTGG	10025
rs766640794	snp	C/G			intron-variant	MED16	GRCh38.p7	19:889306	GAAGACAGCAGCCAC[C/G]AGTTATACATGCAGC	10025
rs766668169	snp	C/G			intron-variant	MED16	GRCh38.p7	19:882513	TGGGCAACACAGCAA[C/G]AGCCTAGCTCAAAAA	10025
rs766668208	snp	A/G	1.86076e-05	0.00305016	intron-variant	MED16	GRCh38.p7	19:871641	AAAAGCACCCACACA[A/G]AGCATGGACCTGTGC	10025
rs766719512	snp	C/T			intron-variant	MED16	GRCh38.p7	19:881842	CTCATGCCGCCCTGC[C/T]CCCATGCCCAGAAGA	10025
rs766729790	snp	C/G	1.6679e-05	0.00288777	missense	MED16	GRCh38.p7	19:873547	TGTCCAGCACAAATT[C/G]CTCCGTCTTGAGGTT	10025
rs766729980	snp	A/G	1.80205e-05	0.00300165	synonymous-codon, intron-variant	MED16	GRCh38.p7	19:877123	AGAGCAGGTGCCGCA[A/G]CGCCAGCCCCACCTC	10025
rs766818759	snp	C/T			intron-variant	MED16	GRCh38.p7	19:874625	GGCCTGGGAGCGTCT[C/T]AGCCCCCAGGAGTAG	10025
rs766839452	snp	C/T	6.81013e-05	0.0058349	synonymous-codon	MED16	GRCh38.p7	19:871993	GGTATCCGAGGTGGC[C/T]GTATACACGGGCAGG	10025
rs766876741	snp	C/T	0.000170289	0.0092258	synonymous-codon	MED16	GRCh38.p7	19:868170	GTGGTGTGTGGACTG[C/T]GGGCCCAGCTGGACA	10025
rs766877668	snp	C/T	1.67489e-05	0.00289381	synonymous-codon	MED16	GRCh38.p7	19:881686	CGATAGGATCCGCCA[C/T]TTGAGAATTGTGGGC	10025
rs766919677	snp	A/G	8.44859e-05	0.00649891	synonymous-codon	MED16	GRCh38.p7	19:872035	CAGAAGGCCCCAGAT[A/G]CGGATGACCACCATC	10025
rs766942790	snp	A/C/T	8.59652e-05	0.00655561	missense, intron-variant	MED16	GRCh38.p7	19:889709	TGGGGTCCCCCTCCA[A/C/T]TAGGCTGCCCACTGA	10025
rs766962354	snp	C/T	2.52848e-05	0.00355552	intron-variant	MED16	GRCh38.p7	19:875474	GGGCAGGAAGCCAGG[C/T]CACCCCAAGGGGCCG	10025
rs766968268	snp	A/G			intron-variant	MED16	GRCh38.p7	19:875175	TCTCAAAAGAGTAAA[A/G]AAAATAAATAAAAAT	10025
rs767013662	snp	A/C	0.000524521	0.016186	intron-variant	MED16	GRCh38.p7	19:873048	AGGTGGGGCAGGGCT[A/C]CGAGGTGGGGCAGGG	10025
rs767032727	snp	A/G	7.81891e-05	0.00625208	synonymous-codon, intron-variant	MED16	GRCh38.p7	19:889782	CTTGATCTGCCCGTC[A/G]GCATCTGCTGACAGG	10025
rs767032764	snp	C/G	1.77707e-05	0.00298077	intron-variant	MED16	GRCh38.p7	19:885730	AAGCAGTGCTTCATT[C/G]CAAGCCTGCCAGCCC	10025
rs767039506	snp	A/C	0.000415024	0.0143993	missense	MED16	GRCh38.p7	19:871169	GGCAGCCAGTCCAGG[A/C]TGGGGATAAGCAGCT	10025
rs767077084	snp	C/T			upstream-variant-2KB	MED16	GRCh38.p7	19:894422	GCCCTCCTTCCACCC[C/T]GGCCTCCCAAAGTGC	10025
rs767133658	snp	A/G			intron-variant	MED16	GRCh38.p7	19:891224	TGCCAGGCCAGAAGT[A/G]GGAAAACAATGGAGG	10025
rs767135697	snp	A/C	2.53604e-05	0.00356084	intron-variant	MED16	GRCh38.p7	19:876925	CGGGGCCCCCACCTG[A/C]CACAGGGCCCCCACC	10025
rs767280588	snp	A/G			intron-variant	MED16	GRCh38.p7	19:885416	AAGGGACCTGCGGGT[A/G]GGATTCGGTTCGGGA	10025
rs767293937	in-del	-/C	3.35334e-05	0.00409458	frameshift-variant	MED16	GRCh38.p7	19:885918	CCACGCTCACGCACA[-/C]CCTTGTAGAACTGCA	10025
rs767306257	in-del	-/TCGTAGCCCCAC	0.000254758	0.0112833	cds-indel, intron-variant	MED16	GRCh38.p7	19:877057	GGGCTGCACGTGCAG[-/TCGTAGCCCCAC]CAGGATGTCCCACCA	10025
rs767347255	snp	A/G	7.7055e-05	0.00620657	intron-variant	MED16	GRCh38.p7	19:871697	CAAGGCAGAGCCACT[A/G]CCACCTGCAGGGGCT	10025
rs767378104	snp	A/G			intron-variant	MED16	GRCh38.p7	19:870077	CCCGGGCCCTGCAAG[A/G]TGACCTCTTGCCCCC	10025
rs767402311	snp	C/T	5.2731e-05	0.00513447	missense	MED16	GRCh38.p7	19:868914	CCAAGGTGCAGCCTC[C/T]GCAGGTGGTCGATCT	10025
rs767418117	snp	A/G	2.07458e-05	0.00322063	missense, utr-variant-5-prime	MED16	GRCh38.p7	19:886152	AACAGCGTGAGCGAC[A/G]GTGAGAACTTGACTC	10025
rs767451367	snp	C/T			intron-variant	MED16	GRCh38.p7	19:870350	TGGATCACCTGAGGT[C/T]AGGAGTTCAAGACCA	10025
rs767544075	snp	C/T	0.000100722	0.00709583	missense, utr-variant-5-prime	MED16	GRCh38.p7	19:890972	ACGCACCCTGGTCAT[C/T]GCTGCGCAGGTCCAT	10025
rs767554568	snp	A/G			intron-variant	MED16	GRCh38.p7	19:888825	CTCACGAAGGGACGA[A/G]AGAAAAGATCTTGTC	10025
rs767632116	snp	A/G	1.65457e-05	0.00287621	missense, utr-variant-5-prime	MED16	GRCh38.p7	19:891049	ACCGATGGGCAGTGG[A/G]TGCTCTTGGACCATT	10025
rs767649213	snp	C/T	1.88685e-05	0.00307146	intron-variant	MED16	GRCh38.p7	19:871605	GACAGCAAACAGGTG[C/T]CTGGAAGTGGCTGCC	10025
rs767663188	snp	A/C/G	0.00032082	0.0126616	synonymous-codon	MED16	GRCh38.p7	19:884937	GAAGATGTTGTTCAC[A/C/G]GGGAGTCCCTCCTTG	10025
rs767704091	snp	C/T	1.90101e-05	0.00308297	missense	MED16	GRCh38.p7	19:868145	CCAGGGATCTGGGGG[C/T]CCTGGGAGAGTGGTG	10025
rs767705462	in-del	-/GG	3.30863e-05	0.00406719	intron-variant	MED16	GRCh38.p7	19:868260	ACAGCCCTGCAGGGC[-/GG]GGGCTGAGGTTAACC	10025
rs767729494	snp	A/G			intron-variant	MED16	GRCh38.p7	19:870934	ATTCGGGGGGACCTG[A/G]GGCAGGACATGCAGG	10025
rs767758538	snp	C/G	1.6669e-05	0.00288691	missense	MED16	GRCh38.p7	19:875328	AGTGGGGGCGCAGCA[C/G]CGACTTCAGGGTGGA	10025
rs767796558	snp	A/G	0.000352849	0.0132778	synonymous-codon	MED16	GRCh38.p7	19:873482	CAGCAGGTACAGCAC[A/G]AAGTCGCCCACCCAC	10025
rs767807781	in-del	-/CCCCACCTGCCACGGGG			intron-variant	MED16	GRCh38.p7	19:876880	CACCTGCCACGGGGC[-/CCCCACCTGCCACGGGG]CCCCACCTGCCACGG	10025
rs767860746	snp	C/T	5.75998e-05	0.00536625	synonymous-codon	MED16	GRCh38.p7	19:880093	GACGGCCATGGTCTG[C/T]AGTGAGAGCCGGTGC	10025
rs767862722	snp	A/G	5.22325e-05	0.00511014	missense, intron-variant	MED16	GRCh38.p7	19:876997	GGGCAGCGGTCTGGC[A/G]CGTGTACTCCTCGTG	10025
rs767879335	snp	A/C/T	3.39952e-05	0.0041227	synonymous-codon, intron-variant	MED16	GRCh38.p7	19:877034	CTCCACCAGGCTCTG[A/C/T]ACCATACTGGGCTGC	10025
rs768018822	snp	A/G	1.69617e-05	0.00291214	missense	MED16	GRCh38.p7	19:885942	AACTGCACGGGCGAC[A/G]CGCTGCTGCCGTCCG	10025
rs768019313	snp	A/G	5.09862e-05	0.00504881	intron-variant	MED16	GRCh38.p7	19:868510	CGCACCTGCGGGGAG[A/G]CAGGCACTGAGCGGG	10025
rs768042281	snp	A/G/T	3.33735e-05	0.00408483	intron-variant	MED16	GRCh38.p7	19:873590	GTCAATGTCTACAAG[A/G/T]AGACGTGGGTCGGGT	10025
rs768104477	in-del	-/ATT			upstream-variant-2KB, nc-transcript-variant	MED16, RNU6-9	GRCh38.p7	19:893585	CGTGAAGCGTTCCAT[-/ATT]TTTTTTTTTTTTTCC	10025
rs768111289	snp	A/G	1.67038e-05	0.00288992	synonymous-codon	MED16	GRCh38.p7	19:881617	GGTGTTGGTGAGCGA[A/G]ATGGGCAGCTTGGGC	10025
rs768140083	snp	C/T	0.000185988	0.00964155	synonymous-codon	MED16	GRCh38.p7	19:868457	CCACTGCTTCACCGC[C/T]GTGGTTCTGTTGGGC	10025
rs768176167	snp	C/T	3.60646e-05	0.00424629	missense	MED16	GRCh38.p7	19:885997	CGCCGGTGAAGGCGA[C/T]GTCGGCCAGGGCCAC	10025
rs768197115	snp	A/G	3.54108e-05	0.00420763	intron-variant	MED16	GRCh38.p7	19:890936	ACCATGCGGCCGGGA[A/G]GGGAAGCAGGTGGGA	10025
rs768203752	snp	C/T	6.77392e-05	0.00581937	synonymous-codon	MED16	GRCh38.p7	19:872071	CCGAAGCATGCCCAG[C/T]GAGGTGCCGTCCCGC	10025
rs768210668	snp	C/T			intron-variant	MED16	GRCh38.p7	19:876350	TCCCTCCTCTCCTTC[C/T]GACGGGCGGGTCTCT	10025
rs768256469	snp	A/G	1.67211e-05	0.00289142	intron-variant	MED16	GRCh38.p7	19:873612	GGGTCGGGTCAGCTC[A/G]GGCCTCTTGTACACA	10025
rs768264009	snp	A/G	2.03044e-05	0.00318618	stop-gained	MED16	GRCh38.p7	19:886057	TGGACGTCAGCACCT[A/G]CCCGCTGGGCTTCAG	10025
rs768275060	snp	G/T	1.89593e-05	0.00307885	missense, intron-variant	MED16	GRCh38.p7	19:889775	TCCAGCACTTGATCT[G/T]CCCGTCGGCATCTGC	10025
rs768284683	snp	A/G	8.58126e-05	0.00654973	intron-variant	MED16	GRCh38.p7	19:881733	AAAAATCAGGGGCAG[A/G]AAAACAGGAAGGCAA	10025
rs768307623	snp	A/G			intron-variant	MED16	GRCh38.p7	19:887344	GACTATGTTAAAGGA[A/G]CACATGTGCCTTTTA	10025
rs768356865	snp	C/T	7.72245e-05	0.0062134	intron-variant	MED16	GRCh38.p7	19:871698	AAGGCAGAGCCACTG[C/T]CACCTGCAGGGGCTT	10025
rs768370300	snp	C/T	0.00048216	0.0155193	intron-variant	MED16	GRCh38.p7	19:884867	AACCGCCCCCGAGGG[C/T]AGGCCCAGGGCCTCC	10025
rs768387690	snp	C/T	4.50867e-05	0.00474777	intron-variant	MED16	GRCh38.p7	19:875503	CGGAGCAGAGGCGCC[C/T]GCCAAGGCTCCAGCT	10025
rs768467810	snp	C/G/T	7.70531e-05	0.00620658	intron-variant	MED16	GRCh38.p7	19:889831	AAGAAGCCATCATTG[C/G/T]GAACCTTCCAGGGAT	10025
rs768502918	in-del	-/AGCTGAGGGGC	2.34607e-05	0.00342488	intron-variant	MED16	GRCh38.p7	19:868354	GGGTAGCTGAGGAGT[-/AGCTGAGGGGC]AGCTGGGCTCAGGGG	10025
rs768544257	snp	G/T	3.52268e-05	0.00419668	intron-variant	MED16	GRCh38.p7	19:873419	GGGGCCCAGGTGGGG[G/T]GCGGGGCCTTAGGGG	10025
rs768550889	snp	A/G	0.00027105	0.0116384	missense	MED16	GRCh38.p7	19:880040	GGGCGCTTCATGGCC[A/G]GCTCATCCACAGGCC	10025
rs768597160	snp	C/T	3.39449e-05	0.00411962	missense	MED16	GRCh38.p7	19:873453	GCATGGCGCACCTGG[C/T]TGGGTAGGCTGGCCA	10025
rs768610500	snp	C/T	1.67225e-05	0.00289154	missense	MED16	GRCh38.p7	19:885900	ATACGGCACTTCTCG[C/T]TCACCACGCTCACGC	10025
rs768631038	snp	C/T	1.69691e-05	0.00291278	missense	MED16	GRCh38.p7	19:881565	CCACCGTACCGAGGC[C/T]AGGGTAGAACTGTGT	10025
rs768637023	snp	A/G	1.65523e-05	0.00287678	missense, utr-variant-5-prime	MED16	GRCh38.p7	19:891031	CAGGCGCAGGCCAGG[A/G]GCACCGATGGGCAGT	10025
rs768685538	snp	C/G	1.66319e-05	0.00288369	missense	MED16	GRCh38.p7	19:885838	TGTCCTTGCGGTTGA[C/G]GTCGGTGGTGCAGCG	10025
rs768692574	snp	A/G	2.27296e-05	0.0033711	intron-variant	MED16	GRCh38.p7	19:868363	AGGAGTAGCTGAGGG[A/G]CAGCTGGGCTCAGGG	10025
rs768742362	snp	A/G			missense	MED16	GRCh38.p7	19:875423	AGCTTGCAGAGCGAG[A/G]CCTTCATGGCCAGGA	10025
rs768797539	snp	C/G			intron-variant	MED16	GRCh38.p7	19:874878	GTCTCTAAAAGCCTG[C/G]GTGTGGTGTAATCCC	10025
rs768811598	snp	A/G			intron-variant	MED16	GRCh38.p7	19:885577	AAGGCGCCCCGAACC[A/G]AGGGATTGGGCGCCT	10025
rs768815695	snp	A/T	2.4702e-05	0.00351431	missense	MED16	GRCh38.p7	19:871931	GGTGCCTCACAGCAG[A/T]TCCAGAGCTTGGTGA	10025
rs768831170	snp	A/G			upstream-variant-2KB	MED16	GRCh38.p7	19:894097	CTGGAGTGCAGTAGC[A/G]CGATCTCAGCTCACT	10025
rs768859674	snp	C/T			intron-variant	MED16	GRCh38.p7	19:882617	CAGCTGGAGCCGGCC[C/T]GCTGGAGCATGTGCG	10025
rs768900748	in-del	-/GGG	1.66735e-05	0.00288729	cds-indel	MED16	GRCh38.p7	19:875316	GCGTGTTGAGAAAGT[-/GGG]GGCGCAGCAGCGACT	10025
rs768910030	snp	A/G	1.74205e-05	0.00295127	intron-variant	MED16	GRCh38.p7	19:886216	ACTGTGGAGAAGGGA[A/G]GGAGGGAGGAGGGGC	10025
rs768958447	snp	A/T	1.68943e-05	0.00290635	intron-variant	MED16	GRCh38.p7	19:877230	GATGGGGCTGCGCCC[A/T]CAGCCGGGAGAGGAA	10025
rs768967589	snp	A/C	1.65696e-05	0.00287828	missense, utr-variant-5-prime	MED16	GRCh38.p7	19:891096	GTAGGCCAAGTCCAT[A/C]ATCCCACCTGCCGCT	10025
rs768975720	in-del	-/C	0.000474217	0.015391	intron-variant	MED16	GRCh38.p7	19:876950	CCACCTGCCACGGGG[-/C]CCCCACCTGCCACGG	10025
rs768991637	snp	C/T	1.84174e-05	0.00303453	intron-variant	MED16	GRCh38.p7	19:889608	TGACATCTCATCTGC[C/T]TCATCCGCTCACTCG	10025
rs768994507	snp	A/G	7.65741e-05	0.00618718	synonymous-codon	MED16	GRCh38.p7	19:880087	GTAGAAGACGGCCAT[A/G]GTCTGCAGTGAGAGC	10025
rs769010211	snp	A/G	2.80289e-05	0.00374348	missense	MED16	GRCh38.p7	19:884995	CTGGTCTGGCTGGAC[A/G]CGCACAAAAGCACCT	10025
rs769048076	snp	A/C/G	5.59074e-05	0.00528688	intron-variant	MED16	GRCh38.p7	19:871626	AGTGGCTGCCATCCC[A/C/G]AAAGCACCCACACAG	10025
rs769098170	snp	C/G/T	4.30672e-05	0.00464023	intron-variant	MED16	GRCh38.p7	19:885028	GGGGGAGGTGGGGGT[C/G/T]AGGGCTGACCCGGCA	10025
rs769102295	snp	A/G	3.7937e-05	0.00435512	intron-variant	MED16	GRCh38.p7	19:871602	AGAGACAGCAAACAG[A/G]TGCCTGGAAGTGGCT	10025
rs769107378	snp	C/G			intron-variant	MED16	GRCh38.p7	19:881017	CCCTCAACCTCTCTG[C/G]AGGCTCTGAGGAACA	10025
rs769130370	snp	A/G	5.00104e-05	0.00500027	missense	MED16	GRCh38.p7	19:875322	TGAGAAAGTGGGGGC[A/G]CAGCAGCGACTTCAG	10025
rs769147742	snp	A/G			intron-variant	MED16	GRCh38.p7	19:881397	GCCTCCTAATTGGGA[A/G]CCCATCAGAACCCAG	10025
rs769177395	snp	A/G			intron-variant	MED16	GRCh38.p7	19:873621	CAGCTCGGGCCTCTT[A/G]TACACACAGGGTGAC	10025
rs769187187	snp	A/G	1.66788e-05	0.00288775	synonymous-codon	MED16	GRCh38.p7	19:875362	GATGGCGATGAGGAA[A/G]AGCTTGGTGTGGTAG	10025
rs769226412	snp	A/G			intron-variant	MED16	GRCh38.p7	19:869717	CCTTCCCCGGAGCAG[A/G]GCTGCTGGAGGTTCA	10025
rs769348205	snp	C/T	1.67114e-05	0.00289057	intron-variant	MED16	GRCh38.p7	19:873606	AGACGTGGGTCGGGT[C/T]AGCTCGGGCCTCTTG	10025
rs769353512	snp	G/T	1.69694e-05	0.0029128	intron-variant	MED16	GRCh38.p7	19:868506	CAGCCGCACCTGCGG[G/T]GAGGCAGGCACTGAG	10025
rs769375639	snp	C/T			intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:892163	TCGCAAAGGCAAAAG[C/T]CCAGGGAGCCTGGAA	10025
rs769385094	snp	A/G	8.0993e-05	0.00636317	missense	MED16	GRCh38.p7	19:886047	AGGCTCTCGGTGGAC[A/G]TCAGCACCTGCCCGC	10025
rs769402935	snp	A/C	1.72528e-05	0.00293703	missense, intron-variant	MED16	GRCh38.p7	19:877097	GGTCACCATGCAGTA[A/C]TCCAGCAGGAAGAGC	10025
rs769405787	snp	C/T	1.70615e-05	0.00292069	splice-acceptor-variant	MED16	GRCh38.p7	19:891150	GGCAGTCACCAGCTC[C/T]TGCGGGAGGGAGGTG	10025
rs769421324	snp	A/G			intron-variant	MED16	GRCh38.p7	19:881086	CAGGGAACCAGGGAA[A/G]AACGGGAGCTGGGGG	10025
rs769457900	snp	C/T	1.86336e-05	0.00305229	utr-variant-3-prime	MED16	GRCh38.p7	19:868060	AAACCGAGGAGACGC[C/T]CGAGCCGGGTCACCA	10025
rs769473262	snp	G/T	1.71105e-05	0.00292489	intron-variant	MED16	GRCh38.p7	19:881729	ACTGAAAAATCAGGG[G/T]CAGGAAAACAGGAAG	10025
rs769515965	in-del	-/GAGCTGCGG			intron-variant	MED16	GRCh38.p7	19:885076	CCACCACCGGAGCCT[-/GAGCTGCGG]GACCCTGGGGCCACG	10025
rs769532976	snp	C/T	1.66804e-05	0.00288789	splice-acceptor-variant	MED16	GRCh38.p7	19:873584	GACCTTGTCAATGTC[C/T]ACAAGGAGACGTGGG	10025
rs769549188	snp	A/G			intron-variant	MED16	GRCh38.p7	19:884699	TGGAAGGATGGAGGA[A/G]TCTATACGCCTAACA	10025
rs769652887	snp	A/G	2.18969e-05	0.00330877	intron-variant	MED16	GRCh38.p7	19:875459	GTGGAGAGGACCTGA[A/G]GGCAGGAAGCCAGGT	10025
rs769706453	snp	C/T	2.32474e-05	0.00340928	intron-variant	MED16	GRCh38.p7	19:868357	TAGCTGAGGAGTAGC[C/T]GAGGGGCAGCTGGGC	10025
rs769746698	snp	C/T			intron-variant	MED16	GRCh38.p7	19:874810	AGAAGGCAGAGGCTG[C/T]GCTGAGCTGGGACTG	10025
rs769749572	snp	C/T	3.74441e-05	0.00432673	missense	MED16	GRCh38.p7	19:871224	CCACCAGCGCCTCGT[C/T]CGGCTCGCTCGCTGG	10025
rs769753856	snp	A/G	2.28334e-05	0.00337878	intron-variant	MED16	GRCh38.p7	19:889813	AGCCGGGAGCCTGAG[A/G]GCAAGAAGCCATCAT	10025
rs769799779	in-del	-/A	0.00274737	0.0369613	intron-variant	MED16	GRCh38.p7	19:876946	GCCCCCACCTGCCAC[-/A]GGGGCCCCACCTGCC	10025
rs769813048	snp	C/T	1.80361e-05	0.00300295	missense, intron-variant	MED16	GRCh38.p7	19:889757	CCAGGTGGTCCGCCA[C/T]GCTCCAGCACTTGAT	10025
rs769852608	snp	A/G	4.02067e-05	0.00448349	intron-variant	MED16	GRCh38.p7	19:875496	AAGGGGCCGGAGCAG[A/G]GGCGCCCGCCAAGGC	10025
rs769885493	in-del	-/CCT	1.67218e-05	0.00289148	intron-variant	MED16	GRCh38.p7	19:873615	TCGGGTCAGCTCGGG[-/CCT]CTTGTACACACAGGG	10025
rs769984169	snp	C/T	0.000102833	0.00716979	intron-variant	MED16	GRCh38.p7	19:885759	CCACGTGATGGCCTG[C/T]GCCCGTTCACCTGCT	10025
rs769998505	snp	C/T	0.000193833	0.00984272	intron-variant	MED16	GRCh38.p7	19:880180	CTGCTTAGACATGGG[C/T]AGGGCCCAGGACACG	10025
rs770002303	snp	G/T	1.66236e-05	0.00288297	missense	MED16	GRCh38.p7	19:885825	ATGGCGGGAAACTTG[G/T]CCTTGCGGTTGAGGT	10025
rs770022225	snp	C/G			upstream-variant-2KB	MED16	GRCh38.p7	19:895114	AAATAAATAAAATAG[C/G]TGGGTGGGGTGATGC	10025
rs770028135	in-del	-/CGT			intron-variant	MED16	GRCh38.p7	19:879076	CCAGCCCCAGCCCCA[-/CGT]GCCCCACGTGCCCCA	10025
rs770044189	in-del	-/G	6.96379e-05	0.00590035	intron-variant	MED16	GRCh38.p7	19:871912	AGGGGAGGGGCGGGC[-/G]GGGGGTGCCTCACAG	10025
rs770067467	snp	A/G			intron-variant	MED16	GRCh38.p7	19:875694	GGGGCCCCTGGTGAT[A/G]TCTGGAGATATTTTT	10025
rs770069504	snp	C/G	1.71725e-05	0.00293018	intron-variant	MED16	GRCh38.p7	19:890954	GAAGCAGGTGGGAGG[C/G]GGACGCACCCTGGTC	10025
rs770087540	snp	A/G	0.000141834	0.00842003	synonymous-codon, utr-variant-5-prime	MED16	GRCh38.p7	19:886141	GCTTGCCGCCGAACA[A/G]CGTGAGCGACGGTGA	10025
rs770095225	snp	G/T	1.78306e-05	0.00298579	intron-variant	MED16	GRCh38.p7	19:881523	TCCCCTGGTGTGAAC[G/T]GAGGCCCCGCGTGGC	10025
rs770106601	in-del	-/AT			frameshift-variant	MED16	GRCh38.p7	19:873579	ATCATGACCTTGTCA[-/AT]GTCTACAAGGAGACG	10025
rs770148345	snp	A/C	0.000283273	0.0118977	stop-gained	MED16	GRCh38.p7	19:868885	AGGCCTTGCATTCCT[A/C]CGTGGGGCAAGCGCC	10025
rs770160006	snp	A/G	1.66726e-05	0.00288722	missense	MED16	GRCh38.p7	19:875303	GGGCTCTTGTCAGGC[A/G]TGTTGAGAAAGTGGG	10025
rs770164373	snp	A/G	3.33862e-05	0.00408558	intron-variant	MED16	GRCh38.p7	19:877200	CAGAGACAGAGCCCA[A/G]GGAGAGCCCGGTGAG	10025
rs770164507	snp	A/G			intron-variant	MED16	GRCh38.p7	19:885666	CCCTGCCCACACCAC[A/G]GTTTAGCCCGTGGAG	10025
rs770245742	snp	A/G			intron-variant	MED16	GRCh38.p7	19:870247	GCGCCCTGTACAGCG[A/G]GGCCAACACACAATC	10025
rs770257847	snp	C/T	1.65564e-05	0.00287714	synonymous-codon	MED16	GRCh38.p7	19:884919	CACGGGGGAGATCTG[C/T]TGGAAGATGTTGTTC	10025
rs770288968	snp	A/G			upstream-variant-2KB	MED16	GRCh38.p7	19:894181	GCTGGGACTACAGGC[A/G]CGCACCACCATGCCC	10025
rs770321904	snp	C/G			intron-variant	MED16	GRCh38.p7	19:870670	GGGGATGGAGTTAGG[C/G]GCACCTAGAAGGAAG	10025
rs770336881	snp	C/T	5.41013e-05	0.00520074	synonymous-codon	MED16	GRCh38.p7	19:868104	GACCCCCGGCCGTCA[C/T]GGACGGTCCTCTGGA	10025
rs770337119	snp	C/G/T	0.000201822	0.0100436	intron-variant	MED16	GRCh38.p7	19:889593	GGTGGCTGGGTAGGG[C/G/T]GACATCTCATCTGCC	10025
rs770359585	snp	A/G			utr-variant-3-prime	MED16	GRCh38.p7	19:868032	TTCAGCGCTCTCCGC[A/G]GGTGAGGCAAGGAAA	10025
rs770473326	snp	A/G	2.44233e-05	0.00349443	synonymous-codon	MED16	GRCh38.p7	19:884976	CCAGCACTCCACGAT[A/G]CTGCTGGTCTGGCTG	10025
rs770498587	snp	A/G	0.000114123	0.00755303	intron-variant	MED16	GRCh38.p7	19:871598	AAGGAGAGACAGCAA[A/G]CAGGTGCCTGGAAGT	10025
rs770516896	snp	A/G			intron-variant	MED16	GRCh38.p7	19:870323	CCCAGCACTTTGGGA[A/G]GGCGAGGCAGGTGGA	10025
rs770516986	snp	C/T			intron-variant	MED16	GRCh38.p7	19:882066	CTTAGCCAGCTCAGC[C/T]GGGATTCCCATCCCT	10025
rs770541011	snp	A/G			upstream-variant-2KB	MED16	GRCh38.p7	19:894245	TTCACCATGTTGGCC[A/G]GGATGGTCTCAGTCT	10025
rs770551860	snp	C/T	0.000242417	0.0110068	intron-variant	MED16	GRCh38.p7	19:871620	CCTGGAAGTGGCTGC[C/T]ATCCCAAAAGCACCC	10025
rs770580004	snp	A/G	5.53776e-05	0.00526172	stop-gained, intron-variant	MED16	GRCh38.p7	19:876979	GGGCCCCCACCTGCT[A/G]CAGGGCAGCGGTCTG	10025
rs770597461	snp	C/T			intron-variant	MED16	GRCh38.p7	19:888766	GAAGCCGGTGCTGCG[C/T]GTACTGCGGCAATGC	10025
rs770599579	snp	C/T	1.69608e-05	0.00291206	synonymous-codon	MED16	GRCh38.p7	19:868451	CTGCTCCCACTGCTT[C/T]ACCGCCGTGGTTCTG	10025
rs770659062	snp	C/T	3.37884e-05	0.00411011	missense	MED16	GRCh38.p7	19:885934	CCTTGTAGAACTGCA[C/T]GGGCGACGCGCTGCT	10025
rs770667975	snp	C/G	1.70464e-05	0.0029194	missense, intron-variant	MED16	GRCh38.p7	19:877021	CCTCGTGCAGCTTCT[C/G]CACCAGGCTCTGTAC	10025
rs770670775	snp	A/G	1.96508e-05	0.00313449	missense	MED16	GRCh38.p7	19:871947	TCCAGAGCTTGGTGA[A/G]CAGGCGGAAGAGCAG	10025
rs770675258	snp	A/G			downstream-variant-500B	MED16	GRCh38.p7	19:867485	CCACTGTGCTGGGAA[A/G]GCCTGCTGGAGACGG	10025
rs770711865	snp	A/G			missense	MED16	GRCh38.p7	19:875388	GGTAGTCGCACACGC[A/G]GGTCACCGTGCAGGG	10025
rs770718364	snp	A/G			intron-variant	MED16	GRCh38.p7	19:873909	CCCCTGCTCCGAGGT[A/G]AACTCTGTGAACACA	10025
rs770721431	snp	A/G	6.67824e-05	0.00577813	missense	MED16	GRCh38.p7	19:881652	CCACGGCCGACACAC[A/G]GTCCAGATCGTTGGT	10025
rs770798762	snp	A/G	0.000456998	0.0151093	synonymous-codon	MED16	GRCh38.p7	19:885980	CACCACGATGTTGCC[A/G]CCGCCGGTGAAGGCG	10025
rs770806785	snp	C/T			upstream-variant-2KB, nc-transcript-variant	MED16, RNU6-9	GRCh38.p7	19:893545	AAGATTAGCATGGCC[C/T]CTGCGCAAGGATGAC	10025
rs770807105	snp	A/G/T	3.41841e-05	0.00413414	intron-variant	MED16	GRCh38.p7	19:881727	CAACTGAAAAATCAG[A/G/T]GGCAGGAAAACAGGA	10025
rs770807891	in-del	-/GA			intron-variant	MED16	GRCh38.p7	19:889467	CACCCTCAGTTAAAT[-/GA]GAGGCCACTGAACAC	10025
rs770809417	snp	A/G	0.000110381	0.00742822	splice-donor-variant	MED16	GRCh38.p7	19:879935	GTGCCCCAGCAGCTC[A/G]CCTTCCCGTGGCTGT	10025
rs770857022	snp	A/T	3.49345e-05	0.00417924	intron-variant	MED16	GRCh38.p7	19:891176	AGGTGTGGTGGGACG[A/T]CTATGTTGGCTGAGC	10025
rs770872284	snp	A/G	1.66665e-05	0.00288669	missense, utr-variant-5-prime	MED16	GRCh38.p7	19:891106	TCCATCATCCCACCT[A/G]CCGCTGGCCGCCGCA	10025
rs770878146	snp	C/G			missense	MED16	GRCh38.p7	19:868110	CGGCCGTCACGGACG[C/G]TCCTCTGGATGCAGA	10025
rs770909988	in-del	-/CGGGCGGGGGGGAGAGGGGAGGGA	8.8881e-05	0.00666578	intron-variant	MED16	GRCh38.p7	19:871907	GGGAGAGGGGAGGGG[-/CGGGCGGGGGGGAGAGGGGAGGGA]CGGGCGGGGGTGCCT	10025
rs770945217	snp	G/T			intron-variant	MED16	GRCh38.p7	19:874827	CTGAGCTGGGACTGC[G/T]TCACCGTGCTGCAAC	10025
rs770949420	in-del	-/C	1.7597e-05	0.00296617	intron-variant	MED16	GRCh38.p7	19:873421	GGCCCAGGTGGGGGG[-/C]GGGGCCTTAGGGGAG	10025
rs770968682	snp	C/T	2.0881e-05	0.00323111	synonymous-codon	MED16	GRCh38.p7	19:879973	CACCAGGGCCAGTGA[C/T]GTCCACGATAGCTGC	10025
rs771058267	snp	A/G	5.10773e-05	0.00505332	utr-variant-5-prime	MED16	GRCh38.p7	19:891146	TGAGGGCAGTCACCA[A/G]CTCCTGCGGGAGGGA	10025
rs771060779	snp	C/G	3.23023e-05	0.00401872	missense	MED16	GRCh38.p7	19:868249	CCACGGCCTTCAACA[C/G]CCCTGCAGGGCGGGC	10025
rs771076722	snp	A/G/T	3.40315e-05	0.00412488	missense, intron-variant	MED16	GRCh38.p7	19:889696	GACAGGGCCACAATG[A/G/T]GGTCCCCCTCCACTA	10025
rs771086860	snp	A/G			intron-variant	MED16	GRCh38.p7	19:884583	CCACGCTCCACAGCC[A/G]CCCACACGCCTGCAG	10025
rs771166547	snp	C/T	5.38411e-05	0.00518822	synonymous-codon, intron-variant	MED16	GRCh38.p7	19:889752	ATTAGCCAGGTGGTC[C/T]GCCATGCTCCAGCAC	10025
rs771196506	snp	A/G	1.79021e-05	0.00299177	intron-variant	MED16	GRCh38.p7	19:873406	TCCTGATGAGATGGG[A/G]GCCCAGGTGGGGGGC	10025
rs771216823	snp	C/G	3.57545e-05	0.004228	intron-variant	MED16	GRCh38.p7	19:881514	GGGCCCAACTCCCCT[C/G]GTGTGAACTGAGGCC	10025
rs771230856	snp	A/G	1.74321e-05	0.00295224	intron-variant	MED16	GRCh38.p7	19:890946	CGGGAGGGGAAGCAG[A/G]TGGGAGGGGGACGCA	10025
rs771268138	snp	A/G	3.63478e-05	0.00426293	intron-variant	MED16	GRCh38.p7	19:890916	CCTGGGGAACAGGGC[A/G]GGACACCATGCGGCC	10025
rs771276414	snp	A/G			intron-variant	MED16	GRCh38.p7	19:890747	TCCCGCACACGGGGC[A/G]ATCTCATGTCTCCTG	10025
rs771287339	snp	A/C/G	0.000262287	0.0114493	intron-variant	MED16	GRCh38.p7	19:871659	CATGGACCTGTGCTA[A/C/G]GAACTGGGGAAATAG	10025
rs771306272	snp	A/G	2.78532e-05	0.00373173	intron-variant	MED16	GRCh38.p7	19:877193	CAGCTGCCAGAGACA[A/G]AGCCCAAGGAGAGCC	10025
rs771325640	snp	C/T	2.47295e-05	0.00351627	intron-variant	MED16	GRCh38.p7	19:880166	GTGGGGCACAGGCAC[C/T]GCTTAGACATGGGCA	10025
rs771354577	snp	C/T			intron-variant	MED16	GRCh38.p7	19:870614	GAAGGGCTGGGTGCC[C/T]GTGTTGGGGGTGGTT	10025
rs771359081	snp	C/T	3.34543e-05	0.00408975	intron-variant	MED16	GRCh38.p7	19:873619	GTCAGCTCGGGCCTC[C/T]TGTACACACAGGGTG	10025
rs771376202	snp	C/G	1.81602e-05	0.00301326	utr-variant-3-prime	MED16	GRCh38.p7	19:868098	CGCCTGGACCCCCGG[C/G]CGTCACGGACGGTCC	10025
rs771390118	snp	A/G	4.00729e-05	0.00447603	synonymous-codon, utr-variant-5-prime	MED16	GRCh38.p7	19:886133	CTCCATGGGCTTGCC[A/G]CCGAACAGCGTGAGC	10025
rs771445317	snp	C/G			intron-variant	MED16	GRCh38.p7	19:880190	ATGGGCAGGGCCCAG[C/G]ACACGCCCGCCGGGG	10025
rs771450779	snp	A/G			intron-variant	MED16	GRCh38.p7	19:887065	GCCTGGGCAACGAGA[A/G]CAAAACTTTGTCTCA	10025
rs771487183	snp	A/C	1.74136e-05	0.00295067	intron-variant	MED16	GRCh38.p7	19:868544	CCACTTCCAGGCGGG[A/C]CTCCCTTACGCCTGC	10025
rs771487206	snp	A/G	5.71108e-05	0.00534342	intron-variant	MED16	GRCh38.p7	19:871685	AATAGCAGATATCAA[A/G]GCAGAGCCACTGCCA	10025
rs771505574	snp	A/G			intron-variant	MED16	GRCh38.p7	19:886393	CTCCTCATCTGTAAG[A/G]TGGAAGGAACGGCAC	10025
rs771555441	snp	A/G	0.000101764	0.00713243	synonymous-codon	MED16	GRCh38.p7	19:875248	AAAGGACCCACCGAC[A/G]TCGGTGATCTTGGTG	10025
rs771616172	in-del	-/TGGGCAGCT	1.67016e-05	0.00288973	cds-indel	MED16	GRCh38.p7	19:881619	TGTTGGTGAGCGAGA[-/TGGGCAGCT]TGGGCAGCGCCACGG	10025
rs771624368	snp	A/C			intron-variant	MED16	GRCh38.p7	19:869855	AGGCTGGGGGTCTGA[A/C]GGGCCTGGGTTCAAA	10025
rs771663625	snp	C/T	0.000173683	0.00931727	synonymous-codon	MED16	GRCh38.p7	19:872101	CAGAAAGCTGTGGCC[C/T]GGCCTCAGCAGGGAA	10025
rs771673602	snp	C/T			intron-variant	MED16	GRCh38.p7	19:886475	CGGGAGTCACCTCCC[C/T]TTTCTGTAAAGGGAC	10025
rs771701938	snp	A/G	5.29395e-05	0.0051446	intron-variant	MED16	GRCh38.p7	19:884877	GAGGGCAGGCCCAGG[A/G]CCTCCGCAGCCGGCG	10025
rs771714315	snp	A/G	5.47315e-05	0.00523094	synonymous-codon	MED16	GRCh38.p7	19:884910	AGACTCACCCACGGG[A/G]GAGATCTGCTGGAAG	10025
rs771718305	snp	C/T	3.92311e-05	0.00442877	missense	MED16	GRCh38.p7	19:880017	GGACGGCGGGGCCCG[C/T]GGTGCGGGGGCGCTT	10025
rs771804202	snp	A/G	1.92706e-05	0.00310402	synonymous-codon	MED16	GRCh38.p7	19:880045	CTTCATGGCCGGCTC[A/G]TCCACAGGCCTCGGG	10025
rs771809348	snp	A/G	1.6941e-05	0.00291036	missense	MED16	GRCh38.p7	19:873457	GGCGCACCTGGTTGG[A/G]TAGGCTGGCCAGCAG	10025
rs771853184	snp	A/G	4.04482e-05	0.00449694	intron-variant	MED16	GRCh38.p7	19:868387	CTCAGGGGTAGCTGA[A/G]GGGCACCCGCCACCA	10025
rs771947568	snp	C/T	1.7376e-05	0.00294749	synonymous-codon	MED16	GRCh38.p7	19:885968	GTCCGCCGTGGCCAC[C/T]ACGATGTTGCCGCCG	10025
rs771956031	snp	C/G	6.96379e-05	0.00590035	intron-variant	MED16	GRCh38.p7	19:871912	GAGGGGAGGGGCGGG[C/G]GGGGGTGCCTCACAG	10025
rs771963117	snp	C/T	1.71258e-05	0.00292619	missense, intron-variant	MED16	GRCh38.p7	19:877011	CGCGTGTACTCCTCG[C/T]GCAGCTTCTCCACCA	10025
rs771963884	snp	C/T			intron-variant	MED16	GRCh38.p7	19:890476	AGAAGAAAATGACTC[C/T]GAAATGTGAACAGTG	10025
rs771993815	snp	A/G	1.68049e-05	0.00289865	synonymous-codon	MED16	GRCh38.p7	19:881581	AGGGTAGAACTGTGT[A/G]TCGCTGGCCACCTTG	10025
rs772006974	snp	A/C/G	0.00127589	0.0252257	synonymous-codon	MED16	GRCh38.p7	19:871942	GCAGATCCAGAGCTT[A/C/G]GTGAGCAGGCGGAAG	10025
rs772010848	in-del	-/GGGGC/GGGGCGGGGGGGGCGGGGG	0.000345894	0.0131471	intron-variant	MED16	GRCh38.p7	19:871903	AGCGGGGAGAGGGGA[-/GGGGC/GGGGCGGGGGGGGCGGGGG]GGGGCGGGCGGGGGT	10025
rs772086033	snp	A/G	2.80069e-05	0.00374201	synonymous-codon	MED16	GRCh38.p7	19:868215	CTCAGAAGCTCTGCT[A/G]GTCACGCAGGCGTCC	10025
rs772090360	snp	A/G	7.71055e-05	0.00620861	synonymous-codon, intron-variant	MED16	GRCh38.p7	19:889779	GCACTTGATCTGCCC[A/G]TCGGCATCTGCTGAC	10025
rs772114594	snp	A/G			downstream-variant-500B	MED16	GRCh38.p7	19:867947	GTCGGGGGCACCGAC[A/G]GCAGGGACGCGGGCC	10025
rs772172157	in-del	-/GCTGGGCTCAGGG	2.24853e-05	0.00335293	intron-variant	MED16	GRCh38.p7	19:868366	AGTAGCTGAGGGGCA[-/GCTGGGCTCAGGG]GTAGCTGAGGGGCAC	10025
rs772228249	snp	A/G	3.12251e-05	0.00395115	missense	MED16	GRCh38.p7	19:885005	TGGACGCGCACAAAA[A/G]CACCTGCGGGGGAGG	10025
rs772256334	snp	A/C	5.0822e-05	0.00504068	missense	MED16	GRCh38.p7	19:871133	TTGGGCTGCAGGCGG[A/C]TAACCAGGCCGTCGC	10025
rs772332785	in-del	-/CCACGGGGCCCCACCTA	6.05235e-05	0.00550074	intron-variant	MED16	GRCh38.p7	19:876959	ACGGGGCCCCACCTG[-/CCACGGGGCCCCACCTA]CCACGGGCCCCCACC	10025
rs772344518	snp	A/C/G			intron-variant	MED16	GRCh38.p7	19:891464	GCACAGCCGGGAGAC[A/C/G]CAGCGGAGGGTCTGC	10025
rs772409671	snp	A/C/G	0.00016829	0.00917163	intron-variant	MED16	GRCh38.p7	19:871655	AGAGCATGGACCTGT[A/C/G]CTAGGAACTGGGGAA	10025
rs772479670	snp	C/G	0.000240402	0.010961	intron-variant	MED16	GRCh38.p7	19:885032	GAGGTGGGGGTGAGG[C/G]CTGACCCGGCACTGC	10025
rs772493085	snp	C/G	1.81138e-05	0.00300941	intron-variant	MED16	GRCh38.p7	19:890913	GCACCTGGGGAACAG[C/G]GCGGGACACCATGCG	10025
rs772524806	snp	A/G	3.72058e-05	0.00431295	intron-variant	MED16	GRCh38.p7	19:871630	GCTGCCATCCCAAAA[A/G]CACCCACACAGAGCA	10025
rs772548695	snp	A/G	2.01185e-05	0.00317157	intron-variant	MED16	GRCh38.p7	19:872146	GGCATCGGTGTGGCT[A/G]GGGCGGCGGGGGGCA	10025
rs772548755	snp	C/T	1.73595e-05	0.00294609	synonymous-codon	MED16	GRCh38.p7	19:875419	CGACAGCTTGCAGAG[C/T]GAGGCCTTCATGGCC	10025
rs772558453	snp	G/T	2.69989e-05	0.00367406	missense	MED16	GRCh38.p7	19:884911	GACTCACCCACGGGG[G/T]AGATCTGCTGGAAGA	10025
rs772577711	snp	C/G			intron-variant	MED16	GRCh38.p7	19:887620	TCAGTGAGCCGAGAT[C/G]GCACCACTGCACTCC	10025
rs772583519	snp	A/G			intron-variant	MED16	GRCh38.p7	19:880750	CACCGGTGAAACCCC[A/G]TCTCTACTAAAATAC	10025
rs772601690	snp	C/T	2.23982e-05	0.00334643	intron-variant	MED16	GRCh38.p7	19:872170	GGGGGCAGATGGCGA[C/T]GGGATGAAGTGTCTT	10025
rs772624083	snp	A/C	0.00180083	0.0299528	intron-variant	MED16	GRCh38.p7	19:871303	TGACTGGGGCACCGC[A/C]CGGCCACCCGGGACG	10025
rs772673165	in-del	-/GTGTGTGGGCCTGTGTGCGCGCATGTGT			intron-variant	MED16	GRCh38.p7	19:877296	TGTGCGCGCACGCCC[-/GTGTGTGGGCCTGTGTGCGCGCATGTGT]CTGTAGCGTCTGTAC	10025
rs772679185	snp	A/G	2.01774e-05	0.0031762	intron-variant	MED16	GRCh38.p7	19:868388	TCAGGGGTAGCTGAG[A/G]GGCACCCGCCACCAG	10025
rs772722748	snp	C/T			intron-variant	MED16	GRCh38.p7	19:884085	GTGGCTTCTGAGGAG[C/T]GCCTGCCCCACCTGC	10025
rs772753521	snp	A/G	1.88945e-05	0.00307358	missense	MED16	GRCh38.p7	19:871239	CCGGCTCGCTCGCTG[A/G]GCCCTCATCGCGACC	10025
rs772760093	snp	A/G	0.000177208	0.00941129	intron-variant	MED16	GRCh38.p7	19:881532	GTGAACTGAGGCCCC[A/G]CGTGGCTGCCGCTGG	10025
rs772846012	snp	A/G	2.81948e-05	0.00375455	intron-variant	MED16	GRCh38.p7	19:889842	ATTGCGAACCTTCCA[A/G]GGATGGGCAGAGCAC	10025
rs772864532	snp	A/G	1.66358e-05	0.00288402	synonymous-codon	MED16	GRCh38.p7	19:885845	GCGGTTGAGGTCGGT[A/G]GTGCAGCGCATGAAC	10025
rs772865068	snp	A/G			intron-variant	MED16	GRCh38.p7	19:889912	CAGTGGAGAGGTCTC[A/G]GCCCAGGTAGGGCAC	10025
rs772883168	snp	C/T			intron-variant	MED16	GRCh38.p7	19:881089	GGAACCAGGGAAGAA[C/T]GGGAGCTGGGGGAAG	10025
rs772885744	snp	C/G	1.67083e-05	0.00289031	missense	MED16	GRCh38.p7	19:873517	AGAGCTGCTGCAGCG[C/G]CTGCAGTGTGTTCAT	10025
rs772923050	snp	C/T			intron-variant	MED16	GRCh38.p7	19:887841	GAGACAACTGGGTCT[C/T]GGGGGCTGGGGTGGG	10025
rs772949626	snp	C/T	1.67542e-05	0.00289427	missense	MED16	GRCh38.p7	19:885915	CTCACCACGCTCACG[C/T]ACACCTTGTAGAACT	10025
rs772982456	snp	C/G	2.53727e-05	0.0035617	intron-variant	MED16	GRCh38.p7	19:876926	GGGGCCCCCACCTGC[C/G]ACAGGGCCCCCACCT	10025
rs773006335	snp	C/G	1.692e-05	0.00290856	missense	MED16	GRCh38.p7	19:873460	GCACCTGGTTGGGTA[C/G]GCTGGCCAGCAGGTA	10025
rs773051100	snp	A/G	3.42132e-05	0.00413587	missense	MED16	GRCh38.p7	19:868435	AGTTCTTGATCCAGC[A/G]CTGCTCCCACTGCTT	10025
rs773059549	snp	A/G			intron-variant	MED16	GRCh38.p7	19:872176	AGATGGCGATGGGAT[A/G]AAGTGTCTTGGGGTC	10025
rs773063472	snp	A/G	0.000233987	0.0108138	intron-variant	MED16	GRCh38.p7	19:871913	AGGGGAGGGGCGGGC[A/G]GGGGTGCCTCACAGC	10025
rs773087136	snp	C/T	1.69594e-05	0.00291194	intron-variant	MED16	GRCh38.p7	19:879888	CAGCTCGCCTTCCCC[C/T]GGTTGTCAATGCCCA	10025
rs773099616	snp	A/G			intron-variant	MED16	GRCh38.p7	19:890517	CACAGCAGATAATAG[A/G]TGGCTTTTTTGCACC	10025
rs773108866	snp	C/T	1.67953e-05	0.00289782	missense	MED16	GRCh38.p7	19:881583	GGTAGAACTGTGTGT[C/T]GCTGGCCACCTTGAG	10025
rs773147642	in-del	-/CCCCACCTGCCACGGGGCCCCCACCTGCCACAGGGC			intron-variant	MED16	GRCh38.p7	19:876898	CCACCTGCCACGGGG[lengthTooLong]CCCCACCTGCCACGG	10025
rs773228944	in-del	-/CTCAGGGGTAGCTGAGGGGCAC	2.21009e-05	0.00332415	intron-variant	MED16	GRCh38.p7	19:868372	TGAGGGGCAGCTGGG[-/CTCAGGGGTAGCTGAGGGGCAC]CCGCCACCAGAGCCC	10025
rs773271447	snp	C/T	3.30857e-05	0.00406716	missense, utr-variant-5-prime	MED16	GRCh38.p7	19:891053	ATGGGCAGTGGGTGC[C/T]CTTGGACCATTTCTC	10025
rs773280948	snp	C/T	0.000110693	0.0074387	intron-variant	MED16	GRCh38.p7	19:879929	CCCCACGTGCCCCAG[C/T]AGCTCACCTTCCCGT	10025
rs773289459	snp	C/G	1.65743e-05	0.00287869	missense, utr-variant-5-prime	MED16	GRCh38.p7	19:891101	CCAAGTCCATCATCC[C/G]ACCTGCCGCTGGCCG	10025
rs773299096	snp	A/G	2.38929e-05	0.00345628	missense	MED16	GRCh38.p7	19:868189	CCCAGCTGGACAAAG[A/G]CAGGGGCTTCCTCAG	10025
rs773333872	snp	C/T			missense	MED16	GRCh38.p7	19:875333	GGGCGCAGCAGCGAC[C/T]TCAGGGTGGAGCTGA	10025
rs773351916	snp	A/G	1.66866e-05	0.00288842	synonymous-codon	MED16	GRCh38.p7	19:875368	GATGAGGAAGAGCTT[A/G]GTGTGGTAGTCGCAC	10025
rs773363566	snp	A/G	5.00063e-05	0.00500006	intron-variant	MED16	GRCh38.p7	19:885035	GTGGGGGTGAGGGCT[A/G]ACCCGGCACTGCTGT	10025
rs773401117	snp	A/G			intron-variant	MED16	GRCh38.p7	19:890047	GGCTCTAGACCCAGC[A/G]CCGGACTCCAGACTG	10025
rs773437277	snp	A/G			intron-variant	MED16	GRCh38.p7	19:875723	TTAGTTGTCACCACT[A/G]GGGGTGCCCCTGCCA	10025
rs773452253	snp	C/T	3.20518e-05	0.00400311	missense	MED16	GRCh38.p7	19:885008	ACGCGCACAAAAGCA[C/T]CTGCGGGGGAGGTGG	10025
rs773487835	in-del	-/C	3.29723e-05	0.00406018	intron-variant	MED16	GRCh38.p7	19:868264	GCCCTGCAGGGCGGG[-/C]TGAGGTTAACCGCGC	10025
rs773488881	snp	C/T			intron-variant	MED16	GRCh38.p7	19:876217	AGAGGGCTGGTCCCA[C/T]GTGCAGCTGCCGGCT	10025
rs773494818	snp	A/G	0.000247617	0.0111242	intron-variant	MED16	GRCh38.p7	19:890333	TCCAGGTAAGCCGGT[A/G]TGTGTCCCACCCCAG	10025
rs773530066	in-del	-/C			upstream-variant-2KB	MED16	GRCh38.p7	19:894749	GGAAACATAGCCAGA[-/C]CCCCGTCTCTACAAA	10025
rs773633080	snp	A/G	2.01282e-05	0.00317233	intron-variant	MED16	GRCh38.p7	19:872147	GCATCGGTGTGGCTG[A/G]GGCGGCGGGGGGCAG	10025
rs773688258	snp	C/G			intron-variant	MED16	GRCh38.p7	19:871634	CCATCCCAAAAGCAC[C/G]CACACAGAGCATGGA	10025
rs773715141	snp	C/G			intron-variant	MED16	GRCh38.p7	19:876126	CTCGGCAGGCTGTGC[C/G]GTGAATGGGATTTTT	10025
rs773735886	snp	A/G	5.07061e-05	0.00503492	synonymous-codon	MED16	GRCh38.p7	19:872032	CTTCAGAAGGCCCCA[A/G]ATGCGGATGACCACC	10025
rs773762839	snp	A/G	1.81194e-05	0.00300988	intron-variant	MED16	GRCh38.p7	19:890914	CACCTGGGGAACAGG[A/G]CGGGACACCATGCGG	10025
rs773784598	in-del	-/G	3.9622e-05	0.00445078	intron-variant	MED16	GRCh38.p7	19:876963	GGCCCCACCTGCCAC[-/G]GGGCCCCCACCTGCT	10025
rs773847391	in-del	-/CT			intron-variant	MED16	GRCh38.p7	19:869516	TCTGACGTAACCGTC[-/CT]CTCTTTCCATCAAGT	10025
rs773847580	snp	C/T	3.64319e-05	0.00426786	missense	MED16	GRCh38.p7	19:886000	CGGTGAAGGCGATGT[C/T]GGCCAGGGCCACGCG	10025
rs773865989	snp	C/T	0.000142203	0.00843096	missense	MED16	GRCh38.p7	19:886060	ACGTCAGCACCTGCC[C/T]GCTGGGCTTCAGCAG	10025
rs773867817	in-del	-/AG			intron-variant	MED16	GRCh38.p7	19:873924	GAACTCTGTGAACAC[-/AG]GGGCATGTCCACAGC	10025
rs773884796	snp	A/T			intron-variant	MED16	GRCh38.p7	19:882103	CTACAATTCCAATAA[A/T]GCCATGCGGGATGGT	10025
rs773888527	snp	C/T			upstream-variant-2KB	MED16	GRCh38.p7	19:894186	GACTACAGGCGCGCA[C/T]CACCATGCCCAACAA	10025
rs773917774	snp	A/G	2.49094e-05	0.00352903	intron-variant	MED16	GRCh38.p7	19:875472	GAGGGCAGGAAGCCA[A/G]GTCACCCCAAGGGGC	10025
rs773996745	in-del	-/T	3.3206e-05	0.00407455	intron-variant	MED16	GRCh38.p7	19:884879	GGCAGGCCCAGGGCC[-/T]TCCGCAGCCGGCGGG	10025
rs774025888	snp	A/G	0.000213744	0.0103357	intron-variant	MED16	GRCh38.p7	19:876965	GCCCCACCTGCCACG[A/G]GCCCCCACCTGCTGC	10025
rs774104421	in-del	-/TATT			upstream-variant-2KB, nc-transcript-variant	MED16, RNU6-9	GRCh38.p7	19:893584	TCGTGAAGCGTTCCA[-/TATT]TTTTTTTTTTTTTCC	10025
rs774121166	snp	A/G	1.66382e-05	0.00288424	intron-variant	MED16	GRCh38.p7	19:884869	CCGCCCCCGAGGGCA[A/G]GCCCAGGGCCTCCGC	10025
rs774122539	snp	A/G	1.68508e-05	0.0029026	missense	MED16	GRCh38.p7	19:881574	CGAGGCCAGGGTAGA[A/G]CTGTGTGTCGCTGGC	10025
rs774138988	snp	C/T	1.76024e-05	0.00296663	intron-variant	MED16	GRCh38.p7	19:873421	GGCCCAGGTGGGGGG[C/T]GGGGCCTTAGGGGAG	10025
rs774144089	snp	C/T	3.38908e-05	0.00411634	intron-variant	MED16	GRCh38.p7	19:885765	GATGGCCTGCGCCCG[C/T]TCACCTGCTCCGACA	10025
rs774150245	snp	A/G	3.37154e-05	0.00410568	intron-variant	MED16	GRCh38.p7	19:875504	GGAGCAGAGGCGCCC[A/G]CCAAGGCTCCAGCTG	10025
rs774157121	snp	A/G			downstream-variant-500B	MED16	GRCh38.p7	19:867852	CTCGGCATCCACTAG[A/G]TGCCCCATAAATGCT	10025
rs774183372	snp	A/G	1.68074e-05	0.00289887	synonymous-codon, utr-variant-5-prime	MED16	GRCh38.p7	19:890970	GGACGCACCCTGGTC[A/G]TCGCTGCGCAGGTCC	10025
rs774185389	snp	C/T			intron-variant	MED16	GRCh38.p7	19:888064	AAAAAAGCAGCCGGG[C/T]GTGGTGGCGGGCGCC	10025
rs774212124	snp	C/T	3.55442e-05	0.00421555	intron-variant	MED16	GRCh38.p7	19:881531	TGTGAACTGAGGCCC[C/T]GCGTGGCTGCCGCTG	10025
rs774256404	snp	A/G/T	0.000473076	0.0153729	intron-variant	MED16	GRCh38.p7	19:868297	AGGAGAGTCCAGGGC[A/G/T]AGCGGTGGCTCTTGC	10025
rs774256518	snp	A/G	0.000257566	0.0113453	intron-variant	MED16	GRCh38.p7	19:871293	TCAGCACCCCTGACT[A/G]GGGCACCGCCCGGCC	10025
rs774333243	snp	G/T	1.69617e-05	0.00291214	missense	MED16	GRCh38.p7	19:873454	CATGGCGCACCTGGT[G/T]GGGTAGGCTGGCCAG	10025
rs774358726	in-del	-/GGC	2.30089e-05	0.00339174	intron-variant	MED16	GRCh38.p7	19:868362	GAGGAGTAGCTGAGG[-/GGC]AGCTGGGCTCAGGGG	10025
rs774377494	snp	C/G	0.000134889	0.00821135	missense	MED16	GRCh38.p7	19:871064	TCGAGCTGCAGGGTG[C/G]CAGCACTGCCAGGCA	10025
rs774386132	snp	A/G	0.000303364	0.0123122	intron-variant	MED16	GRCh38.p7	19:871909	GGAGAGGGGAGGGGC[A/G]GGCGGGGGTGCCTCA	10025
rs774417679	snp	A/G	6.74775e-05	0.00580812	synonymous-codon	MED16	GRCh38.p7	19:881572	ACCGAGGCCAGGGTA[A/G]AACTGTGTGTCGCTG	10025
rs774435071	snp	A/T	3.31592e-05	0.00407167	missense, utr-variant-5-prime	MED16	GRCh38.p7	19:891097	TAGGCCAAGTCCATC[A/T]TCCCACCTGCCGCTG	10025
rs774491918	snp	C/T			intron-variant	MED16	GRCh38.p7	19:888841	AGAAAAGATCTTGTC[C/T]ACTGCATCCCTCCAG	10025
rs774535320	snp	A/G	1.65482e-05	0.00287643	missense, utr-variant-5-prime	MED16	GRCh38.p7	19:891037	CAGGCCAGGGGCACC[A/G]ATGGGCAGTGGGTGC	10025
rs774567580	snp	C/T	2.3548e-05	0.00343124	missense	MED16	GRCh38.p7	19:884930	TCTGCTGGAAGATGT[C/T]GTTCACGGGGAGTCC	10025
rs774574571	snp	A/G/T	1.89888e-05	0.00308124	missense	MED16	GRCh38.p7	19:868144	TCCAGGGATCTGGGG[A/G/T]TCCTGGGAGAGTGGT	10025
rs774574651	snp	A/C	0.000112543	0.00750059	missense	MED16	GRCh38.p7	19:868179	GGACTGCGGGCCCAG[A/C]TGGACAAAGGCAGGG	10025
rs774591866	snp	A/G	4.90136e-05	0.00495019	intron-variant	MED16	GRCh38.p7	19:877232	TGGGGCTGCGCCCTC[A/G]GCCGGGAGAGGAATG	10025
rs774611499	snp	G/T	9.48218e-05	0.0068849	intron-variant	MED16	GRCh38.p7	19:871603	GAGACAGCAAACAGG[G/T]GCCTGGAAGTGGCTG	10025
rs774625387	snp	A/G	1.74799e-05	0.00295629	intron-variant	MED16	GRCh38.p7	19:886220	TGGAGAAGGGAGGGA[A/G]GGAGGAGGGGCCGCT	10025
rs774655560	snp	A/G	0.000145385	0.00852474	synonymous-codon	MED16	GRCh38.p7	19:884997	GGTCTGGCTGGACGC[A/G]CACAAAAGCACCTGC	10025
rs774663158	snp	C/G			intron-variant	MED16	GRCh38.p7	19:873689	GCCCACCCAGTACCA[C/G]GACACAAGGGGACCC	10025
rs774664457	snp	A/C			intron-variant	MED16	GRCh38.p7	19:890622	ACAATGGAGAGAAGA[A/C]GGGCACAGCCACCAC	10025
rs774722712	snp	C/G			intron-variant	MED16	GRCh38.p7	19:871499	TCATTCACTTAAAAA[C/G]TATGTGGGAAGCACT	10025
rs774783810	snp	C/T	3.334e-05	0.00408276	synonymous-codon	MED16	GRCh38.p7	19:875323	GAGAAAGTGGGGGCG[C/T]AGCAGCGACTTCAGG	10025
rs774803587	snp	A/G	1.74163e-05	0.00295091	synonymous-codon, intron-variant	MED16	GRCh38.p7	19:877102	CCATGCAGTACTCCA[A/G]CAGGAAGAGCAGGTG	10025
rs774817166	snp	C/T	1.9143e-05	0.00309372	missense	MED16	GRCh38.p7	19:880089	AGAAGACGGCCATGG[C/T]CTGCAGTGAGAGCCG	10025
rs774840053	in-del	-/G	3.33383e-05	0.00408265	frameshift-variant	MED16	GRCh38.p7	19:875336	GCAGCAGCGACTTCA[-/G]GGGTGGAGCTGATGG	10025
rs774869125	snp	A/C	1.66849e-05	0.00288828	intron-variant	MED16	GRCh38.p7	19:873588	TTGTCAATGTCTACA[A/C]GGAGACGTGGGTCGG	10025
rs774908037	snp	C/G			intron-variant	MED16	GRCh38.p7	19:886486	TCCCCTTTCTGTAAA[C/G]GGACAGACAGCAGCA	10025
rs775058662	in-del	-/GCCCC			intron-variant	MED16	GRCh38.p7	19:879077	CCAGCCCCAGCCCCA[-/GCCCC]ACGTGCCCCAGCAGC	10025
rs775094558	snp	C/T	3.59486e-05	0.00423946	missense	MED16	GRCh38.p7	19:885994	CGCCGCCGGTGAAGG[C/T]GATGTCGGCCAGGGC	10025
rs775188393	in-del	-/CCACGGGCCCCCAC	1.82954e-05	0.00302446	frameshift-variant, intron-variant	MED16	GRCh38.p7	19:876976	ACGGGCCCCCACCTG[-/CCACGGGCCCCCAC]CTGCAGGGCAGCGGT	10025
rs775224906	snp	C/G	6.78587e-05	0.0058245	intron-variant	MED16	GRCh38.p7	19:868291	GCGCCGAGGAGAGTC[C/G]AGGGCGAGCGGTGGC	10025
rs775236722	snp	A/G	1.71056e-05	0.00292446	intron-variant	MED16	GRCh38.p7	19:891152	CAGTCACCAGCTCCT[A/G]CGGGAGGGAGGTGTG	10025
rs775249822	snp	C/T	8.097e-05	0.00636227	missense	MED16	GRCh38.p7	19:886054	CGGTGGACGTCAGCA[C/T]CTGCCCGCTGGGCTT	10025
rs775288266	snp	A/G	8.03939e-05	0.0063396	synonymous-codon	MED16	GRCh38.p7	19:879984	GTGACGTCCACGATA[A/G]CTGCATAGCCTTTAA	10025
rs775288886	snp	C/T	1.81332e-05	0.00301102	missense, intron-variant	MED16	GRCh38.p7	19:889760	GGTGGTCCGCCATGC[C/T]CCAGCACTTGATCTG	10025
rs775379987	snp	A/G	3.28628e-05	0.00405344	intron-variant	MED16	GRCh38.p7	19:868259	CAACAGCCCTGCAGG[A/G]CGGGCTGAGGTTAAC	10025
rs775392479	snp	C/T			intron-variant	MED16	GRCh38.p7	19:882127	GGATGGTCGCACCCA[C/T]AGATCCGCTGCCTGA	10025
rs775397724	snp	C/T	1.69106e-05	0.00290775	missense	MED16	GRCh38.p7	19:872027	CTGGGCTTCAGAAGG[C/T]CCCAGATGCGGATGA	10025
rs775406899	snp	C/G/T	5.12907e-05	0.00506391	missense, intron-variant	MED16	GRCh38.p7	19:889702	GCCACAATGGGGTCC[C/G/T]CCTCCACTAGGCTGC	10025
rs775413413	snp	C/G	9.40035e-05	0.00685514	intron-variant	MED16	GRCh38.p7	19:871666	CTGTGCTAGGAACTG[C/G]GGAAATAGCAGATAT	10025
rs775473937	snp	C/T	0.000212472	0.0103049	intron-variant	MED16	GRCh38.p7	19:875499	GGGCCGGAGCAGAGG[C/T]GCCCGCCAAGGCTCC	10025
rs775473948	snp	A/G/T	0.375	0.216506	intron-variant	MED16	GRCh38.p7	19:872964	GGGAGGGCTCCGAGG[A/G/T]GGGGCAGGGCTCCGA	10025
rs775602068	snp	A/G			intron-variant	MED16	GRCh38.p7	19:889899	GGGGAAGCCAGCCCA[A/G]TGGAGAGGTCTCGGC	10025
rs775633263	in-del	-/AC	1.67318e-05	0.00289234	intron-variant	MED16	GRCh38.p7	19:873623	GCTCGGGCCTCTTGT[-/AC]ACACAGGGTGACCTA	10025
rs775640440	snp	A/G	6.14628e-05	0.00554325	intron-variant	MED16	GRCh38.p7	19:877201	AGAGACAGAGCCCAA[A/G]GAGAGCCCGGTGAGA	10025
rs775669011	snp	A/G	6.74593e-05	0.00580733	synonymous-codon	MED16	GRCh38.p7	19:875254	CCCACCGACGTCGGT[A/G]ATCTTGGTGCAGATC	10025
rs775673533	snp	C/G	2.78424e-05	0.00373101	intron-variant	MED16	GRCh38.p7	19:880182	GCTTAGACATGGGCA[C/G]GGCCCAGGACACGCC	10025
rs775694589	snp	C/T	0.000101925	0.00713809	synonymous-codon, utr-variant-5-prime	MED16	GRCh38.p7	19:886142	CTTGCCGCCGAACAG[C/T]GTGAGCGACGGTGAG	10025
rs775708720	snp	A/G			upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:893465	GGCTTTAAATAGCTG[A/G]TGGTGGAACTCAATA	10025
rs775715714	snp	A/G	0.000101693	0.00712995	intron-variant	MED16	GRCh38.p7	19:868959	GCCCTGGCGGGAGAG[A/G]GGAGAACGTGAGGGA	10025
rs775721262	in-del	-/GGGGGAGAGGGGAGGGGCGGACGT/GGGGGAGAGGGGAGGGGCGGGCGT	0.000160122	0.0089465	intron-variant	MED16	GRCh38.p7	19:871914	GGGAGGGGCGGGCGG[lengthTooLong]GGGTGCCTCACAGCA	10025
rs775760358	snp	C/T	1.6625e-05	0.00288309	missense, intron-variant	MED16	GRCh38.p7	19:877167	ATGGAAGGTGAGAGG[C/T]GGAGCACGCTCAGCT	10025
rs775786366	snp	A/G	2.96555e-05	0.00385057	intron-variant	MED16	GRCh38.p7	19:886211	GCCCGACTGTGGAGA[A/G]GGGAGGGAGGGAGGA	10025
rs775839455	snp	C/G	1.69887e-05	0.00291446	synonymous-codon	MED16	GRCh38.p7	19:872083	CAGCGAGGTGCCGTC[C/G]CGCAGAAAGCTGTGG	10025
rs776037925	snp	C/T	1.97525e-05	0.00314259	intron-variant	MED16	GRCh38.p7	19:871560	TGACACAGCTCACCC[C/T]CCTCACATACACACA	10025
rs776038299	snp	A/G	4.88782e-05	0.00494335	stop-gained	MED16	GRCh38.p7	19:884921	CGGGGGAGATCTGCT[A/G]GAAGATGTTGTTCAC	10025
rs776043084	snp	C/T			intron-variant	MED16	GRCh38.p7	19:877441	TACACTCGTCTGCTT[C/T]ACCTGAGGAGTCTAC	10025
rs776091251	snp	A/G/T	3.79487e-05	0.00435582	intron-variant	MED16	GRCh38.p7	19:871601	GAGAGACAGCAAACA[A/G/T]GTGCCTGGAAGTGGC	10025
rs776122419	snp	C/G	3.52057e-05	0.00419543	synonymous-codon	MED16	GRCh38.p7	19:872110	GTGGCCCGGCCTCAG[C/G]AGGGAACCCTGCCCG	10025
rs776143249	snp	A/G	1.68926e-05	0.0029062	synonymous-codon	MED16	GRCh38.p7	19:885935	CTTGTAGAACTGCAC[A/G]GGCGACGCGCTGCTG	10025
rs776168861	snp	A/G			intron-variant	MED16	GRCh38.p7	19:887720	GACTCAGGCCACAGC[A/G]GGGATGCACCTTGAG	10025
rs776189740	snp	A/G			intron-variant	MED16	GRCh38.p7	19:881045	ACAGCCCTGAGCCCC[A/G]AGCGGGTTTTGATAA	10025
rs776208404	snp	C/G			intron-variant	MED16	GRCh38.p7	19:882407	CTGCACACGCCTGTA[C/G]TCCCAGCTACTCAGG	10025
rs776303638	snp	C/T	1.704e-05	0.00291885	synonymous-codon, intron-variant	MED16	GRCh38.p7	19:877022	CTCGTGCAGCTTCTC[C/T]ACCAGGCTCTGTACC	10025
rs776344333	snp	A/G	5.12781e-05	0.00506324	intron-variant	MED16	GRCh38.p7	19:890279	TCAGCACGGCCTGGC[A/G]CCACAGCCTGCAGAC	10025
rs776363030	snp	A/G	1.76384e-05	0.00296966	synonymous-codon	MED16	GRCh38.p7	19:885983	CACGATGTTGCCGCC[A/G]CCGGTGAAGGCGATG	10025
rs776370630	snp	C/T	0.000200321	0.010006	missense	MED16	GRCh38.p7	19:881655	CGGCCGACACACGGT[C/T]CAGATCGTTGGTGGC	10025
rs776418555	snp	A/C/G	3.41019e-05	0.00412917	utr-variant-5-prime	MED16	GRCh38.p7	19:891149	GGGCAGTCACCAGCT[A/C/G]CTGCGGGAGGGAGGT	10025
rs776453467	snp	C/T			intron-variant	MED16	GRCh38.p7	19:873956	GTGCAGCTGCAGCCA[C/T]CCCCGGCTGGCAGCT	10025
rs776462593	snp	C/T	1.94626e-05	0.00311945	synonymous-codon	MED16	GRCh38.p7	19:871948	CCAGAGCTTGGTGAG[C/T]AGGCGGAAGAGCAGG	10025
rs776471554	snp	C/T	3.34119e-05	0.00408715	missense	MED16	GRCh38.p7	19:875378	AGCTTGGTGTGGTAG[C/T]CGCACACGCGGGTCA	10025
rs776488697	snp	C/G	2.59266e-05	0.00360036	missense	MED16	GRCh38.p7	19:868204	GCAGGGGCTTCCTCA[C/G]AAGCTCTGCTGGTCA	10025
rs776492272	snp	G/T	1.67049e-05	0.00289002	missense	MED16	GRCh38.p7	19:873519	AGCTGCTGCAGCGCC[G/T]GCAGTGTGTTCATGT	10025
rs776518471	snp	C/T	0.000408914	0.014293	missense	MED16	GRCh38.p7	19:871091	GGCAGCGTGGGCGCC[C/T]GGCCAAACTGCAGAC	10025
rs776529826	snp	C/T	0.000127559	0.00798519	synonymous-codon	MED16	GRCh38.p7	19:879940	CCAGCAGCTCACCTT[C/T]CCGTGGCTGTCAATC	10025
rs776572124	in-del	-/T			intron-variant	MED16	GRCh38.p7	19:880390	GCCCCTCCCCGCCCC[-/T]CCCAGCTGGGCCCAT	10025
rs776618063	snp	A/G	4.20053e-05	0.00458267	missense	MED16	GRCh38.p7	19:879974	ACCAGGGCCAGTGAC[A/G]TCCACGATAGCTGCA	10025
rs776639051	snp	C/T			missense, utr-variant-5-prime	MED16	GRCh38.p7	19:886135	CCATGGGCTTGCCGC[C/T]GAACAGCGTGAGCGA	10025
rs776648930	in-del	-/TGGATGACACAGTGAGA	9.01754e-05	0.00671413	frameshift-variant	MED16	GRCh38.p7	19:868912	GCCAAGGTGCAGCCT[-/TGGATGACACAGTGAGA]CCGCAGGTGGTCGAT	10025
rs776675168	in-del	-/AT	0.000622157	0.0176264	frameshift-variant, utr-variant-5-prime	MED16	GRCh38.p7	19:891130	CGCCGCAAATCACAC[-/AT]GAGGGCAGTCACCAG	10025
rs776714863	snp	A/G	0.000102276	0.00715034	synonymous-codon, intron-variant	MED16	GRCh38.p7	19:889698	CAGGGCCACAATGGG[A/G]TCCCCCTCCACTAGG	10025
rs776734241	in-del	-/CCC			intron-variant	MED16	GRCh38.p7	19:879075	ACCAGCCCCAGCCCC[-/CCC]AGCCCCACGTGCCCC	10025
rs776739650	snp	A/T			intron-variant	MED16	GRCh38.p7	19:882866	CACAGAGCCTTGACC[A/T]CCTGCAAACCCGTAT	10025
rs776779745	snp	A/T	5.27218e-05	0.00513401	intron-variant	MED16	GRCh38.p7	19:880176	GGCACTGCTTAGACA[A/T]GGGCAGGGCCCAGGA	10025
rs776796243	snp	A/G	2.23977e-05	0.00334639	missense, intron-variant	MED16	GRCh38.p7	19:877165	CCATGGAAGGTGAGA[A/G]GCGGAGCACGCTCAG	10025
rs776798544	snp	C/T			intron-variant	MED16	GRCh38.p7	19:888910	AGACGCACAGAGGCA[C/T]GAAGCTGGGGTGGCT	10025
rs776804974	snp	A/G	1.7033e-05	0.00291826	intron-variant	MED16	GRCh38.p7	19:885046	GGCTGACCCGGCACT[A/G]CTGTGGTGGCCACGC	10025
rs776817481	snp	A/G			downstream-variant-500B	MED16	GRCh38.p7	19:867935	GTCGTGGGTGGGGTC[A/G]GGGGCACCGACGGCA	10025
rs776829756	in-del	-/AGGGGGAGCGGGGAGGGGCA/GGGCA	7.58581e-05	0.00615819	intron-variant	MED16	GRCh38.p7	19:871909	GAGAGGGGAGGGGCG[-/AGGGGGAGCGGGGAGGGGCA/GGGCA]GGCGGGGGTGCCTCA	10025
rs776842964	snp	A/T	1.80592e-05	0.00300487	intron-variant	MED16	GRCh38.p7	19:890919	GGGGAACAGGGCGGG[A/T]CACCATGCGGCCGGG	10025
rs776863442	snp	A/G			intron-variant	MED16	GRCh38.p7	19:885585	CCGAACCGAGGGATT[A/G]GGCGCCTCCAGATGC	10025
rs776867516	snp	A/T			intron-variant	MED16	GRCh38.p7	19:874885	AAAGCCTGGGTGTGG[A/T]GTAATCCCAGCCTTT	10025
rs776886424	snp	A/G	0.000111352	0.00746082	utr-variant-3-prime	MED16	GRCh38.p7	19:868067	GGAGACGCCCGAGCC[A/G]GGTCACCACAAGGTC	10025
rs776962671	snp	C/T	6.88871e-05	0.00586846	intron-variant	MED16	GRCh38.p7	19:885755	CAGCCCACGTGATGG[C/T]CTGCGCCCGTTCACC	10025
rs776990453	snp	C/T	1.67455e-05	0.00289352	intron-variant	MED16	GRCh38.p7	19:873624	CTCGGGCCTCTTGTA[C/T]ACACAGGGTGACCTA	10025
rs777029313	snp	A/G	3.4724e-05	0.00416663	intron-variant	MED16	GRCh38.p7	19:890948	GGAGGGGAAGCAGGT[A/G]GGAGGGGGACGCACC	10025
rs777099954	snp	C/G	1.76045e-05	0.00296681	intron-variant	MED16	GRCh38.p7	19:868549	TCCAGGCGGGCCTCC[C/G]TTACGCCTGCCCCAC	10025
rs777107748	snp	A/G	1.90558e-05	0.00308667	intron-variant	MED16	GRCh38.p7	19:871686	ATAGCAGATATCAAG[A/G]CAGAGCCACTGCCAC	10025
rs777124816	snp	C/T	0.000126893	0.00796433	utr-variant-3-prime	MED16	GRCh38.p7	19:868099	GCCTGGACCCCCGGC[C/T]GTCACGGACGGTCCT	10025
rs777184628	snp	A/C/T	3.38022e-05	0.00411098	missense	MED16	GRCh38.p7	19:872036	AGAAGGCCCCAGATG[A/C/T]GGATGACCACCATCA	10025
rs777186635	snp	C/T	1.69321e-05	0.0029096	missense	MED16	GRCh38.p7	19:875250	AGGACCCACCGACGT[C/T]GGTGATCTTGGTGCA	10025
rs777192255	snp	C/G	2.00166e-05	0.00316353	missense, utr-variant-5-prime	MED16	GRCh38.p7	19:886134	TCCATGGGCTTGCCG[C/G]CGAACAGCGTGAGCG	10025
rs777220120	snp	C/G			intron-variant	MED16	GRCh38.p7	19:869913	TGACCCCAGATGAGT[C/G]GGGTGACAAGGTCCC	10025
rs777294692	snp	A/G	1.74303e-05	0.00295209	missense	MED16	GRCh38.p7	19:872102	AGAAAGCTGTGGCCC[A/G]GCCTCAGCAGGGAAC	10025
rs777296856	snp	C/T	1.66735e-05	0.00288729	missense	MED16	GRCh38.p7	19:875349	TCAGGGTGGAGCTGA[C/T]GGCGATGAGGAAGAG	10025
rs777298547	snp	C/T	3.91642e-05	0.004425	intron-variant	MED16	GRCh38.p7	19:886250	TCAGGCTCATGGGGG[C/T]TGCCCCATGACCCCC	10025
rs777300157	in-del	-/AG	3.41282e-05	0.00413073	intron-variant	MED16	GRCh38.p7	19:881725	GCCAACTGAAAAATC[-/AG]GGGCAGGAAAACAGG	10025
rs777379899	snp	C/T	2.01586e-05	0.00317473	missense	MED16	GRCh38.p7	19:868163	TGGGAGAGTGGTGTG[C/T]GGACTGCGGGCCCAG	10025
rs777383203	snp	C/G	4.68604e-05	0.00484025	intron-variant	MED16	GRCh38.p7	19:890263	TGGGGACGGGGCATG[C/G]TCAGCACGGCCTGGC	10025
rs777412850	snp	A/G	0.000180587	0.00950057	intron-variant	MED16	GRCh38.p7	19:871014	AGTCCTGTGTTTGGG[A/G]ACCAATGCAGGGACA	10025
rs777423516	snp	C/G	1.91331e-05	0.00309292	intron-variant	MED16	GRCh38.p7	19:871592	CCCGACAAGGAGAGA[C/G]AGCAAACAGGTGCCT	10025
rs777459198	snp	A/G	0.000193756	0.00984076	synonymous-codon	MED16	GRCh38.p7	19:884973	GGACCAGCACTCCAC[A/G]ATGCTGCTGGTCTGG	10025
rs777653749	snp	C/G/T	7.84473e-05	0.00626246	missense	MED16	GRCh38.p7	19:880110	GTGAGAGCCGGTGCA[C/G/T]GATGTGGACGCTGCC	10025
rs777655660	snp	C/G	1.70819e-05	0.00292244	missense, intron-variant	MED16	GRCh38.p7	19:877015	TGTACTCCTCGTGCA[C/G]CTTCTCCACCAGGCT	10025
rs777658127	snp	A/G	3.48961e-05	0.00417694	synonymous-codon	MED16	GRCh38.p7	19:885971	CGCCGTGGCCACCAC[A/G]ATGTTGCCGCCGCCG	10025
rs777672797	snp	C/G			intron-variant	MED16	GRCh38.p7	19:883032	CGCCCCAGCGCCGGG[C/G]GAGGCAGCTGCCATG	10025
rs777688024	in-del	-/G	8.92355e-05	0.00667906	intron-variant	MED16	GRCh38.p7	19:873415	GATGGGGGCCCAGGT[-/G]GGGGGCGGGGCCTTA	10025
rs777693984	snp	C/T			intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:891495	GCTGGCCCAGGTGAG[C/T]GATGATGGGGGCAGC	10025
rs777734614	snp	A/G	1.69608e-05	0.00291206	synonymous-codon	MED16	GRCh38.p7	19:872007	CCGTATACACGGGCA[A/G]GCAGCTGGGCTTCAG	10025
rs777743498	snp	A/G	3.40298e-05	0.00412477	synonymous-codon, intron-variant	MED16	GRCh38.p7	19:877064	CACGTGCAGCAGGAT[A/G]TCCCACCAGTCGTAG	10025
rs777746157	snp	C/G	1.98667e-05	0.00315166	missense	MED16	GRCh38.p7	19:886026	ACGCGGCCGCGCAGC[C/G]GGCACAGGCTCTCGG	10025
rs777766805	snp	G/T	5.11452e-05	0.00505668	intron-variant	MED16	GRCh38.p7	19:881723	TCGCCAACTGAAAAA[G/T]CAGGGGCAGGAAAAC	10025
rs777777627	snp	G/T			intron-variant	MED16	GRCh38.p7	19:884732	CTCAGAATGCTGGCA[G/T]GCGCGCGGTCACACC	10025
rs777803715	snp	G/T			upstream-variant-2KB, nc-transcript-variant	MED16, RNU6-9	GRCh38.p7	19:893529	TTGGAACGATACAGA[G/T]AAGATTAGCATGGCC	10025
rs777806963	snp	C/T			intron-variant	MED16	GRCh38.p7	19:874813	AGGCAGAGGCTGCGC[C/T]GAGCTGGGACTGCGT	10025
rs777822721	snp	C/T	1.66732e-05	0.00288727	missense	MED16	GRCh38.p7	19:873561	TCCTCCGTCTTGAGG[C/T]TGATCATGACCTTGT	10025
rs777877843	snp	C/G/T	0.000121504	0.00779351	missense	MED16	GRCh38.p7	19:871979	GACATGCTGTCCTGG[C/G/T]TATCCGAGGTGGCCG	10025
rs777881921	snp	C/T			intron-variant	MED16	GRCh38.p7	19:880552	GGGTCTGCCATTGTA[C/T]GAGGGCCGGGGGGAG	10025
rs777921128	snp	G/T	1.82663e-05	0.00302206	missense	MED16	GRCh38.p7	19:875432	AGCGAGGCCTTCATG[G/T]CCAGGATCCGGGTGG	10025
rs777954866	snp	A/C			intron-variant	MED16	GRCh38.p7	19:876578	TAAGGAAGGAAACTG[A/C]TTCTCTGAGGTGCAG	10025
rs778110546	snp	C/T	3.48997e-05	0.00417716	intron-variant	MED16	GRCh38.p7	19:891174	GGAGGTGTGGTGGGA[C/T]GTCTATGTTGGCTGA	10025
rs778121751	snp	A/G	1.66849e-05	0.00288828	synonymous-codon	MED16	GRCh38.p7	19:885806	CAGGAACTTGAGGTG[A/G]GTGATGGCGGGAAAC	10025
rs778154491	snp	A/G	1.76833e-05	0.00297344	intron-variant	MED16	GRCh38.p7	19:890937	CCATGCGGCCGGGAG[A/G]GGAAGCAGGTGGGAG	10025
rs778160451	snp	A/G			intron-variant	MED16	GRCh38.p7	19:870685	GGCACCTAGAAGGAA[A/G]CAGCAGTCATGGCCA	10025
rs778213553	snp	C/T	1.78921e-05	0.00299094	intron-variant	MED16	GRCh38.p7	19:881511	TCAGGGCCCAACTCC[C/T]CTGGTGTGAACTGAG	10025
rs778233710	snp	A/G	7.18107e-05	0.00599168	intron-variant	MED16	GRCh38.p7	19:880161	GCCCTGTGGGGCACA[A/G]GCACTGCTTAGACAT	10025
rs778243329	snp	C/T	2.14941e-05	0.0032782	missense, intron-variant	MED16	GRCh38.p7	19:889801	TCTGCTGACAGGAGC[C/T]GGGAGCCTGAGGGCA	10025
rs778270193	snp	C/G			intron-variant	MED16	GRCh38.p7	19:882640	CATGTGCGGCCAGTG[C/G]ACAGGCCACGCCACC	10025
rs778279119	snp	A/C			intron-variant	MED16	GRCh38.p7	19:883061	TGACGACCACACCCC[A/C]AGCTAGTGGCCAGGG	10025
rs778312840	snp	A/G	1.7948e-05	0.00299561	intron-variant	MED16	GRCh38.p7	19:873404	GGTCCTGATGAGATG[A/G]GGGCCCAGGTGGGGG	10025
rs778323285	snp	A/T			intron-variant	MED16	GRCh38.p7	19:886832	TATAATCCCAGCACT[A/T]TGGGGGGCTGAGGCA	10025
rs778334666	snp	C/T	1.86517e-05	0.00305377	intron-variant	MED16	GRCh38.p7	19:871637	TCCCAAAAGCACCCA[C/T]ACAGAGCATGGACCT	10025
rs778387054	snp	C/T			intron-variant	MED16	GRCh38.p7	19:871481	GCCTGTCATGAGACT[C/T]CCTCATTCACTTAAA	10025
rs778397040	snp	C/T	5.11958e-05	0.00505918	missense	MED16	GRCh38.p7	19:875244	TGGAAAAGGACCCAC[C/T]GACGTCGGTGATCTT	10025
rs778447221	snp	A/G	1.66272e-05	0.00288328	synonymous-codon, utr-variant-5-prime	MED16	GRCh38.p7	19:890991	GCGCAGGTCCATGGT[A/G]AAGGCGATGAGATTT	10025
rs778489503	snp	C/T	3.62614e-05	0.00425786	intron-variant	MED16	GRCh38.p7	19:886242	GGGGCCGCTCAGGCT[C/T]ATGGGGGCTGCCCCA	10025
rs778512018	snp	C/G	1.93512e-05	0.0031105	missense	MED16	GRCh38.p7	19:880041	GGCGCTTCATGGCCG[C/G]CTCATCCACAGGCCT	10025
rs778530858	snp	A/G	9.26569e-05	0.00680587	synonymous-codon	MED16	GRCh38.p7	19:868931	CAGGTGGTCGATCTT[A/G]GGCTGGCCTGGGGCC	10025
rs778536856	snp	A/G	1.72943e-05	0.00294055	synonymous-codon	MED16	GRCh38.p7	19:872098	CCGCAGAAAGCTGTG[A/G]CCCGGCCTCAGCAGG	10025
rs778559911	snp	C/T	9.73454e-05	0.0069759	intron-variant	MED16	GRCh38.p7	19:871705	AGCCACTGCCACCTG[C/T]AGGGGCTTATGTTCT	10025
rs778563442	snp	A/G			synonymous-codon, intron-variant	MED16	GRCh38.p7	19:889745	CCCAGCTATTAGCCA[A/G]GTGGTCCGCCATGCT	10025
rs778591565	snp	C/T	1.67142e-05	0.00289081	missense	MED16	GRCh38.p7	19:875286	CGGTCAGCCGGTCGC[C/T]GGGGCTCTTGTCAGG	10025
rs778614904	snp	A/G			intron-variant	MED16	GRCh38.p7	19:870591	AAAAAAAAGGGAGAG[A/G]GTGAATGGAAGGGCT	10025
rs778653723	snp	A/G	0.000960153	0.0218896	intron-variant	MED16	GRCh38.p7	19:890433	GCAGGCCTGTGAGGC[A/G]CCACAACTGTGTCTT	10025
rs778656186	in-del	-/AGGGCTCCGAGGTGGGGGAGGGCTCCGAGGTGGGGC	0.00100222	0.022363	intron-variant	MED16	GRCh38.p7	19:872934	GGCTTCATGGAGAGG[lengthTooLong]AGGGCTCCGAGGTGG	10025
rs778663529	snp	C/T			intron-variant	MED16	GRCh38.p7	19:875963	AAAAAATAGAAACAA[C/T]TAAAAACAAAAATGA	10025
rs778682095	snp	A/G	0.000101616	0.00712724	missense	MED16	GRCh38.p7	19:872072	CGAAGCATGCCCAGC[A/G]AGGTGCCGTCCCGCA	10025
rs778711464	snp	A/T					GRCh38.p7	19:871544	CACTGGGATGTAAGA[A/T]TGACACAGCTCACCC	10025
rs778772888	snp	A/C/G	5.55667e-05	0.00527076	missense	MED16	GRCh38.p7	19:884909	GAGACTCACCCACGG[A/C/G]GGAGATCTGCTGGAA	10025
rs778794525	snp	A/G	3.8192e-05	0.00436973	synonymous-codon	MED16	GRCh38.p7	19:880072	CGGGGCCGCGGAGCT[A/G]TAGAAGACGGCCATG	10025
rs778833842	in-del	-/GGGAGGGGCGAGGGGGAGCA	1.95969e-05	0.00313019	intron-variant	MED16	GRCh38.p7	19:871899	GGGGAGCGGGGAGAG[-/GGGAGGGGCGAGGGGGAGCA]GGGAGGGGCGGGCGG	10025
rs778877685	snp	C/T	0.000131036	0.00809325	intron-variant	MED16	GRCh38.p7	19:890259	TCTGTGGGGACGGGG[C/T]ATGGTCAGCACGGCC	10025
rs778888127	snp	C/T	1.6674e-05	0.00288734	missense	MED16	GRCh38.p7	19:873555	ACAAATTCCTCCGTC[C/T]TGAGGTTGATCATGA	10025
rs778920960	in-del	-/C	1.70717e-05	0.00292157	frameshift-variant, intron-variant	MED16	GRCh38.p7	19:889699	GGGCCACAATGGGGT[-/C]CCCCCTCCACTAGGC	10025
rs778924170	snp	G/T	1.73222e-05	0.00294292	missense	MED16	GRCh38.p7	19:868422	CCACCGCACAGGCAG[G/T]TCTTGATCCAGCGCT	10025
rs778965860	snp	C/T			intron-variant	MED16	GRCh38.p7	19:869594	CTCCCACAGTGAGCA[C/T]GAGGAAGAAAATGCT	10025
rs778966446	snp	C/T	1.67301e-05	0.00289219	synonymous-codon	MED16	GRCh38.p7	19:885905	GCACTTCTCGCTCAC[C/T]ACGCTCACGCACACC	10025
rs779017470	snp	A/G			intron-variant	MED16	GRCh38.p7	19:870147	TGGGCCATATGCTAA[A/G]GCGTCTCTCTCCATC	10025
rs779042101	snp	C/T			upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:893437	GCCTATGTGTACAGA[C/T]ATTTGTTCCAGGGGC	10025
rs779045261	snp	C/G	3.55271e-05	0.00421454	missense	MED16	GRCh38.p7	19:871964	AGGCGGAAGAGCAGG[C/G]ACATGCTGTCCTGGG	10025
rs779120195	snp	C/G	1.68952e-05	0.00290642	synonymous-codon	MED16	GRCh38.p7	19:868487	CGACTTGAGCATGGT[C/G]ACACAGCCGCACCTG	10025
rs779212483	snp	A/G	1.6865e-05	0.00290383	utr-variant-5-prime	MED16	GRCh38.p7	19:891135	CAAATCACACATGAG[A/G]GCAGTCACCAGCTCC	10025
rs779223212	snp	A/G			downstream-variant-500B	MED16	GRCh38.p7	19:867582	AGCAGAGAGCAGCTG[A/G]AGAAACATAACAGGG	10025
rs779224550	snp	A/G			intron-variant	MED16	GRCh38.p7	19:881315	TTGTTGATTTGCAAT[A/G]ACTCTTTACATATTA	10025
rs779264813	snp	C/T	1.74821e-05	0.00295647	stop-gained, intron-variant	MED16	GRCh38.p7	19:889731	GCCCACTGAGCTCTC[C/T]CAGCTATTAGCCAGG	10025
rs779295818	snp	C/G			intron-variant	MED16	GRCh38.p7	19:880717	CTGAGCTCAGGGGTT[C/G]GAGACCAGCCTGGGC	10025
rs779344335	snp	C/T	2.2154e-05	0.00332814	intron-variant	MED16	GRCh38.p7	19:872167	GCGGGGGGCAGATGG[C/T]GATGGGATGAAGTGT	10025
rs779404094	snp	A/G			intron-variant	MED16	GRCh38.p7	19:887481	CACCATCCTGGCCAA[A/G]ATAGTGAAACCCCGT	10025
rs779404264	snp	C/G	2.28658e-05	0.00338118	synonymous-codon	MED16	GRCh38.p7	19:879964	GTCAATCCCCACCAG[C/G]GCCAGTGACGTCCAC	10025
rs779456489	snp	A/C			intron-variant	MED16	GRCh38.p7	19:887090	GTCTCAAAAACAAAA[A/C]AAAAAAGAACAAGAA	10025
rs779463892	snp	C/T	0.000420418	0.0144925	intron-variant	MED16	GRCh38.p7	19:885743	TTCCAAGCCTGCCAG[C/T]CCACGTGATGGCCTG	10025
rs779476612	snp	A/G	2.32221e-05	0.00340742	intron-variant	MED16	GRCh38.p7	19:880155	GGGCCAGCCCTGTGG[A/G]GCACAGGCACTGCTT	10025
rs779526785	in-del	-/GTAGCTGAGGA	0.000404904	0.0142228	intron-variant	MED16	GRCh38.p7	19:868341	AGGGGCAGCTGAGGG[-/GTAGCTGAGGA]GTAGCTGAGGGGCAG	10025
rs779533218	snp	A/G			intron-variant	MED16	GRCh38.p7	19:884258	GAAAACCAAGCGGCT[A/G]TTCTGGTCCCCGGTC	10025
rs779608628	snp	C/T			intron-variant	MED16	GRCh38.p7	19:886774	TCTTTCAACGTGAGT[C/T]TTTTAAAAGATGGGG	10025
rs779618893	snp	A/G	2.56545e-05	0.00358142	intron-variant	MED16	GRCh38.p7	19:877183	GGAGCACGCTCAGCT[A/G]CCAGAGACAGAGCCC	10025
rs779622707	in-del	-/GGGGAGGGGCGGCCGGGGGGGAGC/GGGGAGGGGCGGGCGGGGGGGAGC/GGGGAGGGGCGGGCGGGGGGGGGAGC	0.0029243	0.0381261	intron-variant	MED16	GRCh38.p7	19:871898	CGGGGAGCGGGGAGA[lengthTooLong]GGGGAGGGGCGGGCG	10025
rs779646068	snp	A/G	1.66554e-05	0.00288573	intron-variant	MED16	GRCh38.p7	19:884864	ACCAACCGCCCCCGA[A/G]GGCAGGCCCAGGGCC	10025
rs779657503	snp	C/G/T	5.4389e-05	0.0052146	intron-variant	MED16	GRCh38.p7	19:890912	GGCACCTGGGGAACA[C/G/T]GGCGGGACACCATGC	10025
rs779686718	snp	C/G	1.72496e-05	0.00293675	intron-variant	MED16	GRCh38.p7	19:875231	GAGGCCCCGGGCGTG[C/G]AAAAGGACCCACCGA	10025
rs779702660	snp	A/G			intron-variant	MED16	GRCh38.p7	19:885639	TCCCCTGGAGCCCCC[A/G]GGAGGGACCGGCCCT	10025
rs779708686	snp	A/G			intron-variant	MED16	GRCh38.p7	19:873722	ACCGGGAACGAGAAG[A/G]GGGCGATGGCGTTGC	10025
rs779733947	snp	A/G	5.90313e-05	0.00543251	missense	MED16	GRCh38.p7	19:880011	TTAAGTGGACGGCGG[A/G]GCCCGCGGTGCGGGG	10025
rs779760016	snp	C/G			intron-variant	MED16	GRCh38.p7	19:883148	CATTCCTAAATGAGG[C/G]GGGACTTGAGGCAGG	10025
rs779812234	snp	C/G	1.82277e-05	0.00301886	utr-variant-3-prime	MED16	GRCh38.p7	19:868093	AGGTCCGCCTGGACC[C/G]CCGGCCGTCACGGAC	10025
rs779817079	snp	C/G	1.6715e-05	0.00289089	intron-variant	MED16	GRCh38.p7	19:873609	CGTGGGTCGGGTCAG[C/G]TCGGGCCTCTTGTAC	10025
rs779906578	snp	C/T	3.95382e-05	0.00444607	missense	MED16	GRCh38.p7	19:886108	CGCTGACCGTCACCG[C/T]GATCCAGCCCTCCAT	10025
rs779925024	snp	A/C/G	2.19147e-05	0.00331012	missense, stop-gained, utr-variant-5-prime	MED16	GRCh38.p7	19:886168	GTGAGAACTTGACTC[A/C/G]GGAGAACTTCTCCCC	10025
rs779954578	snp	C/G	0.000107904	0.00734441	intron-variant	MED16	GRCh38.p7	19:890111	TCCGGGTCGCCACCC[C/G]TGGCCACGTGGGACC	10025
rs780047562	snp	A/G			intron-variant	MED16	GRCh38.p7	19:890484	ATGACTCCGAAATGT[A/G]AACAGTGGGAGCCTC	10025
rs780058395	snp	A/C	2.31008e-05	0.00339851	intron-variant	MED16	GRCh38.p7	19:889815	CCGGGAGCCTGAGGG[A/C]AAGAAGCCATCATTG	10025
rs780072047	snp	A/T	2.10844e-05	0.0032468	intron-variant	MED16	GRCh38.p7	19:871267	ACCTGCGGAGAGAGG[A/T]GGCGGAAGTCTCAGC	10025
rs780076530	snp	C/G/T	5.81168e-05	0.00539032	synonymous-codon	MED16	GRCh38.p7	19:880039	GGGGCGCTTCATGGC[C/G/T]GGCTCATCCACAGGC	10025
rs780089387	in-del	-/TGTCAATGCCCAGCAGCTCACCTTCCCCTGGC	0.00011781	0.00767405	intron-variant	MED16	GRCh38.p7	19:879891	TCGCCTTCCCCTGGT[lengthTooLong]TGTCAATGCCCACCA	10025
rs780109775	snp	A/G	3.46795e-05	0.00416396	missense, intron-variant	MED16	GRCh38.p7	19:876999	GCAGCGGTCTGGCGC[A/G]TGTACTCCTCGTGCA	10025
rs780159236	snp	G/T			upstream-variant-2KB, downstream-variant-500B	MED16, RNU6-9	GRCh38.p7	19:893962	GACCCCGTTGAGTAT[G/T]CCTACTTCCAACCCT	10025
rs780169770	snp	A/G	6.90584e-05	0.00587575	intron-variant	MED16	GRCh38.p7	19:868360	CTGAGGAGTAGCTGA[A/G]GGGCAGCTGGGCTCA	10025
rs780177317	in-del	-/GGGCCCCACCTGCCACA	2.34673e-05	0.00342536	intron-variant	MED16	GRCh38.p7	19:876947	CCCCCACCTGCCACG[-/GGGCCCCACCTGCCACA]GGGCCCCACCTGCCA	10025
rs780275287	snp	A/T	1.92844e-05	0.00310513	intron-variant	MED16	GRCh38.p7	19:871584	ACACACAACCCGACA[A/T]GGAGAGACAGCAAAC	10025
rs780386131	snp	C/T	0.000271444	0.0116468	synonymous-codon	MED16	GRCh38.p7	19:871126	GGGCTGCTTGGGCTG[C/T]AGGCGGCTAACCAGG	10025
rs780386381	snp	C/T	3.43867e-05	0.00414634	synonymous-codon	MED16	GRCh38.p7	19:885956	CGCGCTGCTGCCGTC[C/T]GCCGTGGCCACCACG	10025
rs780390076	snp	A/G	1.68329e-05	0.00290106	missense, utr-variant-5-prime	MED16	GRCh38.p7	19:891130	CGCCGCAAATCACAC[A/G]TGAGGGCAGTCACCA	10025
rs780449574	snp	A/T			intron-variant	MED16	GRCh38.p7	19:887673	TCTGTCTCAAAAAAA[A/T]TGTATTTGGTTATTT	10025
rs780486093	snp	A/G	5.00296e-05	0.00500123	synonymous-codon	MED16	GRCh38.p7	19:875353	GGTGGAGCTGATGGC[A/G]ATGAGGAAGAGCTTG	10025
rs780486311	snp	A/G	8.09968e-05	0.00636332	synonymous-codon	MED16	GRCh38.p7	19:884991	GCTGCTGGTCTGGCT[A/G]GACGCGCACAAAAGC	10025
rs780507926	snp	A/G	1.66999e-05	0.00288958	synonymous-codon	MED16	GRCh38.p7	19:881625	TGAGCGAGATGGGCA[A/G]CTTGGGCAGCGCCAC	10025
rs780508070	snp	A/G	0.000239297	0.0109358	intron-variant	MED16	GRCh38.p7	19:877226	GTGAGATGGGGCTGC[A/G]CCCTCAGCCGGGAGA	10025
rs780537339	snp	A/G	0.000209806	0.0102401	intron-variant	MED16	GRCh38.p7	19:872137	CCCGAAAGAGGCATC[A/G]GTGTGGCTGGGGCGG	10025
rs780568543	in-del	-/AA			intron-variant	MED16	GRCh38.p7	19:888525	CGAGACTCTGTCTCC[-/AA]AAAAAAAAAAAAAAA	10025
rs780593484	snp	C/G			downstream-variant-500B	MED16	GRCh38.p7	19:867638	CAGCATGCAGAGACA[C/G]AGAGACCATACACAG	10025
rs780595894	snp	A/C	1.67854e-05	0.00289697	intron-variant	MED16	GRCh38.p7	19:879914	GCCCACCAGCCCCGG[A/C]CCCACGTGCCCCAGC	10025
rs780612317	snp	C/T			intron-variant	MED16	GRCh38.p7	19:880842	AGGAAGGAGAATCGC[C/T]TGAACCCAGGAGGCG	10025
rs780677190	snp	C/T			intron-variant	MED16	GRCh38.p7	19:888625	ACCGTGTGGGCTGCA[C/T]ACTCTCAATGGGTGA	10025
rs780707693	snp	C/G/T	3.72705e-05	0.00431673	intron-variant	MED16	GRCh38.p7	19:871625	AAGTGGCTGCCATCC[C/G/T]AAAAGCACCCACACA	10025
rs780725521	snp	A/G	1.69055e-05	0.00290731	missense	MED16	GRCh38.p7	19:875402	CGGGTCACCGTGCAG[A/G]GCGACAGCTTGCAGA	10025
rs780726408	snp	C/T			intron-variant	MED16	GRCh38.p7	19:885476	GTCCGGGGGCCCCAG[C/T]GTCCTCACAGGGTCC	10025
rs780747728	snp	A/G	2.17772e-05	0.00329972	missense	MED16	GRCh38.p7	19:880142	TCGTGGAAGGCCAGG[A/G]CCAGCCCTGTGGGGC	10025
rs780757089	snp	A/C/T	0.000186561	0.00965672	intron-variant	MED16	GRCh38.p7	19:871650	CACACAGAGCATGGA[A/C/T]CTGTGCTAGGAACTG	10025
rs780775004	snp	C/T	0.000236551	0.0108729	missense	MED16	GRCh38.p7	19:880113	AGAGCCGGTGCACGA[C/T]GTGGACGCTGCCGTC	10025
rs780780947	snp	A/C	8.47943e-05	0.00651076	intron-variant	MED16	GRCh38.p7	19:872160	TGGGGCGGCGGGGGG[A/C]AGATGGCGATGGGAT	10025
rs780835365	snp	A/G	5.97675e-05	0.00546628	synonymous-codon	MED16	GRCh38.p7	19:868227	GCTGGTCACGCAGGC[A/G]TCCGGCCCACGGCCT	10025
rs780835415	snp	A/G	1.95842e-05	0.00312917	missense, intron-variant	MED16	GRCh38.p7	19:877147	CCACCTCCAGCGGGT[A/G]GCCCATGGAAGGTGA	10025
rs780954977	snp	C/T	1.72121e-05	0.00293356	intron-variant	MED16	GRCh38.p7	19:868536	GCGGGTTCCCACTTC[C/T]AGGCGGGCCTCCCTT	10025
rs781006972	snp	A/G			intron-variant	MED16	GRCh38.p7	19:874759	GTGTCTGTAATCCCA[A/G]CTACTCCAGAGGCTG	10025
rs781031377	snp	C/T	1.71929e-05	0.00293192	missense, intron-variant	MED16	GRCh38.p7	19:877092	TAGCCGGTCACCATG[C/T]AGTACTCCAGCAGGA	10025
rs781101363	in-del	-/CCAGCAGGT	3.37747e-05	0.00410928	cds-indel	MED16	GRCh38.p7	19:873466	GGTTGGGTAGGCTGG[-/CCAGCAGGT]ACAGCACGAAGTCGC	10025
rs781113104	snp	C/T	3.33522e-05	0.0040835	missense	MED16	GRCh38.p7	19:873580	TCATGACCTTGTCAA[C/T]GTCTACAAGGAGACG	10025
rs781136216	snp	G/T	1.68091e-05	0.00289901	intron-variant	MED16	GRCh38.p7	19:875490	CACCCCAAGGGGCCG[G/T]AGCAGAGGCGCCCGC	10025
rs781136454	in-del	-/CCACCTGCCACGGGGCCCCACCTG	2.2779e-05	0.00337476	intron-variant	MED16	GRCh38.p7	19:876936	CCTGCCACAGGGCCC[-/CCACCTGCCACGGGGCCCCACCTG]CCACGGGCCCCCACC	10025
rs781166568	snp	G/T	6.68304e-05	0.0057802	intron-variant	MED16	GRCh38.p7	19:873603	AGGAGACGTGGGTCG[G/T]GTCAGCTCGGGCCTC	10025
rs781169860	snp	A/T	1.98489e-05	0.00315025	missense	MED16	GRCh38.p7	19:886102	CCAGGCCGCTGACCG[A/T]CACCGCGATCCAGCC	10025
rs781210774	snp	A/G	0.000107691	0.00733716	intron-variant	MED16	GRCh38.p7	19:890928	GGCGGGACACCATGC[A/G]GCCGGGAGGGGAAGC	10025
rs781219707	snp	C/T	0.000101659	0.00712875	missense	MED16	GRCh38.p7	19:872012	TACACGGGCAGGCAG[C/T]TGGGCTTCAGAAGGC	10025
rs781280725	snp	G/T	1.94079e-05	0.00311505	missense	MED16	GRCh38.p7	19:880031	GCGGTGCGGGGGCGC[G/T]TCATGGCCGGCTCAT	10025
rs781289909	snp	A/G	0.000135254	0.00822245	intron-variant	MED16	GRCh38.p7	19:886233	GAGGGAGGAGGGGCC[A/G]CTCAGGCTCATGGGG	10025
rs781294415	snp	A/G			upstream-variant-2KB	MED16	GRCh38.p7	19:894922	AACCACATCTCTACT[A/G]AAAATACAAAAATAT	10025
rs781297145	snp	A/G			upstream-variant-2KB, nc-transcript-variant	MED16, RNU6-9	GRCh38.p7	19:893555	TGGCCCCTGCGCAAG[A/G]ATGACACGCAAATTC	10025
rs781327317	snp	A/G	0.000131559	0.00810938	intron-variant	MED16	GRCh38.p7	19:871275	AGAGAGGTGGCGGAA[A/G]TCTCAGCACCCCTGA	10025
rs781374698	snp	A/G	1.798e-05	0.00299827	missense, intron-variant	MED16	GRCh38.p7	19:889753	TTAGCCAGGTGGTCC[A/G]CCATGCTCCAGCACT	10025
rs781477444	snp	A/G			intron-variant	MED16	GRCh38.p7	19:877462	AGGAGTCTACCCCGT[A/G]AAAGGCGGTCCTCTC	10025
rs781491575	snp	A/G	1.83323e-05	0.00302751	intron-variant	MED16	GRCh38.p7	19:868403	GGGCACCCGCCACCA[A/G]AGCCCACCGCACAGG	10025
rs781536370	snp	A/C	6.80836e-05	0.00583414	intron-variant	MED16	GRCh38.p7	19:889811	GGAGCCGGGAGCCTG[A/C]GGGCAAGAAGCCATC	10025
rs781553278	snp	C/T			upstream-variant-2KB	MED16	GRCh38.p7	19:894138	CCTTCCAGGCTCAAG[C/T]GATTCTCCTGCCTCA	10025
rs781564163	snp	A/G	0.00010494	0.00724286	missense, utr-variant-5-prime	MED16	GRCh38.p7	19:886200	AAGCTGGAGGCGCCC[A/G]ACTGTGGAGAAGGGA	10025
rs781590715	snp	C/G	4.38222e-05	0.00468072	intron-variant	MED16	GRCh38.p7	19:877224	CGGTGAGATGGGGCT[C/G]CGCCCTCAGCCGGGA	10025
rs781591784	snp	G/T	1.70711e-05	0.00292152	intron-variant	MED16	GRCh38.p7	19:873443	TTAGGGGAGAGCATG[G/T]CGCACCTGGTTGGGT	10025
rs781662198	snp	A/G	1.65888e-05	0.00287996	synonymous-codon, utr-variant-5-prime	MED16	GRCh38.p7	19:891009	GGCGATGAGATTTCG[A/G]CAGGACCAGGCGCAG	10025
rs781672581	snp	A/T	1.65573e-05	0.00287721	missense, utr-variant-5-prime	MED16	GRCh38.p7	19:891091	CAGACGTAGGCCAAG[A/T]CCATCATCCCACCTG	10025
rs781688988	snp	C/T			intron-variant	MED16	GRCh38.p7	19:881900	TGCCTCGGCCACTCA[C/T]TGGTTCCAGGATGGG	10025
rs781709839	snp	A/G	3.9198e-05	0.0044269	intron-variant	MED16	GRCh38.p7	19:871709	ACTGCCACCTGCAGG[A/G]GCTTATGTTCTGGCG	10025
rs781723251	in-del	-/CACA	0.00297251	0.0384372	intron-variant	MED16	GRCh38.p7	19:871635	CATCCCAAAAGCACC[-/CACA]CAGAGCATGGACCTG	10025
rs781737389	snp	A/G	2.76729e-05	0.00371963	synonymous-codon	MED16	GRCh38.p7	19:871927	CGGGGGTGCCTCACA[A/G]CAGATCCAGAGCTTG	10025
rs781739437	snp	A/G	1.81191e-05	0.00300985	synonymous-codon	MED16	GRCh38.p7	19:868943	CTTGGGCTGGCCTGG[A/G]GCCCTGGCGGGAGAG	10025
rs796167324	in-del	CTGGTTGTCAATGCCCAGCAGCTCGCCTTCCCC/G			intron-variant	MED16	GRCh38.p7	19:879855	CAGCTCACCTTCCCC[lengthTooLong]GGTTGTCAATGCCCA	10025
rs796180699	snp	A/G			intron-variant	MED16	GRCh38.p7	19:882632	TGCTGGAGCATGTGC[A/G]GCCAGTGGACAGGCC	10025
rs796205681	snp	A/C			intron-variant	MED16	GRCh38.p7	19:877765	TGGTTGTCAATGCCC[A/C]CCAGCCCCAGCCCCA	10025
rs796297860	snp	A/G			intron-variant	MED16	GRCh38.p7	19:876512	GAGCCGTCCAGGGGG[A/G]ATCAGGCCTTACCTG	10025
rs796311784	snp	C/G			intron-variant	MED16	GRCh38.p7	19:878502	GTCAATGCCCACCAG[C/G]CCCAGCCCCACGTGC	10025
rs796446948	snp	C/T			intron-variant	MED16	GRCh38.p7	19:883759	GAAGGTGCAGGTCTG[C/T]GCAGCCACACGGGGT	10025
rs796453547	snp	C/G			intron-variant	MED16	GRCh38.p7	19:884298	GGGCGTCCCTGCTTC[C/G]CTCCAGCCCCAGGAT	10025
rs796460298	in-del	-/A			intron-variant	MED16	GRCh38.p7	19:887085	CTTTGTCTCAAAAAC[-/A]AAAAAAAAAAAGAAC	10025
rs796481976	snp	A/G			intron-variant	MED16	GRCh38.p7	19:877808	GCCCCACGTGCCCCA[A/G]CAGCTCGCCTTCCCG	10025
rs796597768	snp	C/T			intron-variant	MED16	GRCh38.p7	19:891340	AGGGCCAGTCCTGGG[C/T]CTGTGGGCTTCTACT	10025
rs796615774	snp	C/G			intron-variant	MED16	GRCh38.p7	19:878503	TCAATGCCCACCAGC[C/G]CCAGCCCCACGTGCC	10025
rs796625127	snp	G/T			intron-variant	MED16	GRCh38.p7	19:890853	AGGGCCAGGGTGAGT[G/T]AGAGGTGGCCTGAGA	10025
rs796634288	snp	C/T			intron-variant, upstream-variant-2KB	MED16, RNU6-9	GRCh38.p7	19:892667	TCCCTCTCCAGGCCC[C/T]GCACCGATAACCCCG	10025
rs796728470	snp	A/G			intron-variant	MED16	GRCh38.p7	19:887884	GTGATGCAGGATGGG[A/G]ACTGGGTTTCCTTTT	10025
rs796860008	snp	G/T			intron-variant	MED16	GRCh38.p7	19:874334	AGCCAGGATGATCTC[G/T]ATCTCCTGACCTCGT	10025
rs796882817	snp	A/G			intron-variant	MED16	GRCh38.p7	19:870720	TGGAGAACATGGAGG[A/G]AAGGAGCCGTATGGA	10025
rs796913259	in-del	-/AC			intron-variant	MED16	GRCh38.p7	19:886270	CCATGACCCCCAGAA[-/AC]ACGCGCACAGAAGAA	10025
rs796943938	snp	C/G			intron-variant	MED16	GRCh38.p7	19:887711	CGAGGCTCTGACTCA[C/G]GCCACAGCGGGGATG	10025
rs796991269	snp	A/G			intron-variant	MED16	GRCh38.p7	19:876320	CCCTTCTGGCACGTG[A/G]GCCTCCGTATCCGCT	10025

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