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

SART1

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs570312050	snp	C/T	0.000399281	0.0141238	intron-variant	SART1	GRCh38.p7	11:65965559	GGAGAAGGGAAGGGC[C/T]GTGGTCGGTAGCATC	9092
rs570672501	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime	SART1, TSGA10IP	GRCh38.p7	11:65960389	GGGTTTCAGGAGAGA[C/T]TGGGATTGTGTGCAC	9092
rs570758719	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, downstream-variant-500B	SART1, TSGA10IP	GRCh38.p7	11:65960769	TCAAGAAAAAAACTC[A/G]TACACACAGATGTGC	9092
rs570767360	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65975323	GTCCAGGCTGGTCTC[A/G]AACTCCTGGGCTCAA	9092
rs570858839	snp	C/T	0.000399281	0.0141238	intron-variant	SART1	GRCh38.p7	11:65978310	TTTGTCTCCCTGCAG[C/T]CCCAGCCCCAGCCCC	9092
rs570967383	snp	C/G	3.3145e-05	0.0040708	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65977788	TGACAAGTACAGCCG[C/G]AGGGAGGAATACCGA	9092
rs570985400	snp	A/G	0.000399281	0.0141238	intron-variant	SART1	GRCh38.p7	11:65967110	AGTGGAATTGAGATA[A/G]TAACCACCCCACATG	9092
rs571081144	snp	C/T	0.000399281	0.0141238	intron-variant	SART1	GRCh38.p7	11:65966623	GGCTCCTGCCCTGCC[C/T]GCAGGCACTGAGAAG	9092
rs571109150	snp	G/T	0.000399281	0.0141238	intron-variant	SART1	GRCh38.p7	11:65973624	GTGTGCGTGCCCGGG[G/T]CCCACCCCACACCTC	9092
rs571187336	snp	A/G	0.000798403	0.0199641	intron-variant	SART1	GRCh38.p7	11:65973043	ACCAGACGTGGTGGC[A/G]GGCACCTGTAGTCCC	9092
rs571218204	snp	A/G	0.00199481	0.0315187	utr-variant-3-prime, downstream-variant-500B	SART1	GRCh38.p7	11:65979309	TAGAAAGTGGAAGGC[A/G]GTTTTAGAAACTCAT	9092
rs571389729	snp	A/G	9.74516e-05	0.00697971	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65967735	GAGGAGGACGAGGCG[A/G]AGCTGGAGCTGCAGA	9092
rs571513595	snp	G/T	0.000399281	0.0141238	intron-variant	SART1	GRCh38.p7	11:65968686	GCTGGCATTTAGGCA[G/T]TAGACCAACCAGCAG	9092
rs571578219	snp	A/G	0.000399281	0.0141238	intron-variant	SART1	GRCh38.p7	11:65962324	ACAAAGCGAGACTCT[A/G]TCTCAAAAAGAAAAA	9092
rs571934041	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65973564	AGAGTCCTCAGCCAC[A/G]CTACTCACAGCCATG	9092
rs571972773	snp	A/G	0.000798403	0.0199641	intron-variant	SART1	GRCh38.p7	11:65963441	TAAAGGAGAAGGTAG[A/G]ATGCAGGATGGGAAT	9092
rs571973714	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65964837	CTTGCTGCAGACTGC[A/G]CTGTGCGGGGGTGGG	9092
rs571996981	snp	A/G	0.000399281	0.0141238	intron-variant	SART1	GRCh38.p7	11:65962617	TAAGAACTGTAGATT[A/G]TCTTGAGGATAGTAG	9092
rs572059280	snp	A/G	0.000399281	0.0141238	intron-variant	SART1	GRCh38.p7	11:65968889	TGTTCTGTGTTTGTT[A/G]ATTCATTCCATCCTC	9092
rs572109410	snp	A/G	0.000798403	0.0199641	intron-variant	SART1	GRCh38.p7	11:65968530	GCTGGGCACTCAGTA[A/G]ACCAAGATAACGTGC	9092
rs572134770	snp	C/T	0.00159617	0.0282053	intron-variant	SART1	GRCh38.p7	11:65974633	GCAGTGAGCCTATAT[C/T]GCCCCATTGCACTCC	9092
rs572367702	snp	C/T	0.000798403	0.0199641	intron-variant	SART1	GRCh38.p7	11:65969981	CCCTCCTCAGCCTCC[C/T]AAAGTGCTGGAATTA	9092
rs572408252	snp	C/T	0.000399281	0.0141238	intron-variant	SART1	GRCh38.p7	11:65970354	TTTTTAGTTTTTTGT[C/T]GTAAGCAGCATCCAA	9092
rs573098116	snp	A/G	0.000399281	0.0141238	intron-variant	SART1	GRCh38.p7	11:65977266	CTGTGGCATCTGTCC[A/G]TCTGCTCTGCCTTTG	9092
rs573217720	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, downstream-variant-500B	SART1, TSGA10IP	GRCh38.p7	11:65960456	CTCTGTCACCAGGCC[A/G]GAGTGCAATGGTGTG	9092
rs573265472	snp	A/G	0.000399281	0.0141238	intron-variant	SART1	GRCh38.p7	11:65966763	GCCCCAGTCTGTTTC[A/G]GCTCTGCCATGCTGC	9092
rs573280641	snp	G/T	0.000798403	0.0199641	intron-variant	SART1	GRCh38.p7	11:65973201	ATTGAGAACGTAAGT[G/T]TTTTGTTTTTTGTTT	9092
rs573529147	snp	A/G	0.000798403	0.0199641	intron-variant	SART1	GRCh38.p7	11:65962404	TGCTTGAGGACAGAG[A/G]GCTTCTGTTTTCCTC	9092
rs573535747	snp	C/T	0.00279162	0.0372561	utr-variant-3-prime, downstream-variant-500B	SART1	GRCh38.p7	11:65979346	GCTCTCTCCTGGCCT[C/T]GGGGGCTGCACAGGT	9092
rs573722961	snp	A/G	3.34734e-05	0.00409091	intron-variant	SART1	GRCh38.p7	11:65978963	GTGGGGAGGGGTGGC[A/G]TGGCCTGTGCCCGCC	9092
rs573772079	snp	A/G	0.0006226	0.0176327	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	SART1	GRCh38.p7	11:65962026	CACGCACGGGCGGGA[A/G]CGCAGCCAGGCAGAG	9092
rs574155416	snp	A/C/T	0.000136557	0.00826208	intron-variant	SART1	GRCh38.p7	11:65965028	AGGGGGCAGGGTGAG[A/C/T]GGCTCCCTCCTCTCC	9092
rs574509812	snp	A/C			intron-variant	SART1	GRCh38.p7	11:65962224	TTACCAGCTCTATTA[A/C]ATAGTCTTTCTACGG	9092
rs574525272	snp	C/T	0.00083888	0.020463	intron-variant	SART1	GRCh38.p7	11:65965263	GAAGGGCTGGGGAGG[C/T]CACCATCCTTGGCTG	9092
rs574591665	snp	G/T	0.00398564	0.0444627	intron-variant	SART1	GRCh38.p7	11:65963469	AATGCAGGAAAGGAA[G/T]AGTTTTTTTTTTGTT	9092
rs574808204	snp	A/G	0.000399281	0.0141238	intron-variant	SART1	GRCh38.p7	11:65970957	AGGAGGGGGATGGTG[A/G]GATTCATGAGCTGAG	9092
rs574845401	snp	A/C/G/T	9.53683e-05	0.00690488	intron-variant	SART1	GRCh38.p7	11:65976784	GAGGGCCGCGCCGCT[A/C/G/T]GGGGGTGGGCGTTTG	9092
rs575502837	snp	A/G	0.00279162	0.0372561	intron-variant	SART1	GRCh38.p7	11:65978418	CAAGCTGGTCTCCCG[A/G]CCTCTGCTGGGGCCC	9092
rs575524852	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65972373	TTATCTATTTGGGGA[A/G]AAAATGAAATTGGGT	9092
rs575544683	snp	A/G	0.000399281	0.0141238	intron-variant	SART1	GRCh38.p7	11:65966876	GGTTGCTGTGAGGAT[A/G]AGTGACAGCGTGGGT	9092
rs575666487	snp	A/T	0.000399281	0.0141238	missense, utr-variant-5-prime, nc-transcript-variant	SART1	GRCh38.p7	11:65962076	AGCGGGAGAAGCGCG[A/T]TGACGGCTACGAGGC	9092
rs575828216	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, downstream-variant-500B	SART1, TSGA10IP	GRCh38.p7	11:65960596	TATTTTTAGTAGAGA[C/T]GGGGTTTTACCATGT	9092
rs575943233	snp	A/G	0.0023933	0.0345097	intron-variant	SART1	GRCh38.p7	11:65974598	GGAGGAGGATCACTT[A/G]AACCTGGGAGGTGGA	9092
rs575986079	snp	A/G	0.000399281	0.0141238	intron-variant	SART1	GRCh38.p7	11:65968426	GGGCCCTGGGCTCAT[A/G]GAGCTGGCTTTCTAG	9092
rs576098924	snp	A/G	0.000798403	0.0199641	intron-variant	SART1	GRCh38.p7	11:65973856	AAAACAAATCACAGA[A/G]GAGTCATACAGTGTG	9092
rs576156683	snp	G/T			intron-variant	SART1	GRCh38.p7	11:65971513	GGATGGTGGGATTCA[G/T]GAGCTGAGGAGGGGG	9092
rs576595123	snp	A/C	1.65597e-05	0.00287743	intron-variant	SART1	GRCh38.p7	11:65964468	GGAAATGCACATGGC[A/C]CCCTGTGTCTTTAAT	9092
rs576894224	snp	C/G	0.000399281	0.0141238	intron-variant	SART1	GRCh38.p7	11:65964918	GGGTCCTGTTGTGCT[C/G]CATGGGTTGGCCAGG	9092
rs577134022	snp	G/T	0.000318167	0.0126088	upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime	SART1, TSGA10IP	GRCh38.p7	11:65959977	GCAAACACAGTATGA[G/T]ATTTCTGGTGGTGGG	9092
rs577168800	snp	C/T	0.000399281	0.0141238	intron-variant	SART1	GRCh38.p7	11:65972361	TGGGACAGTCAGTTA[C/T]CTATTTGGGGAAAAA	9092
rs577195670	snp	C/G	0.00358779	0.0422022	intron-variant	SART1	GRCh38.p7	11:65978467	GTGCTCTTTTCCCAT[C/G]CCCTTCCCACTGCAC	9092
rs577437939	snp	C/T	0.0023933	0.0345097	upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime	SART1, TSGA10IP	GRCh38.p7	11:65960407	GGATTGTGTGCACTG[C/T]GCTTTTTTTTTTTTT	9092
rs577480150	snp	C/T	0.00105642	0.0229585	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65978894	CATCGTGCTCAGCGG[C/T]AGCGGCAAGAGCATG	9092
rs577517454	snp	A/G	0.00279162	0.0372561	intron-variant	SART1	GRCh38.p7	11:65973180	CTCCGTCTCAAAAAA[A/G]AAGAAATTGAGAACG	9092
rs577860130	snp	C/T	0.000399281	0.0141238	intron-variant	SART1	GRCh38.p7	11:65966964	GAGGTAGACAGCTGG[C/T]GCGGTAGGCGTCTTC	9092
rs578051718	snp	C/T	4.95516e-05	0.00497728	missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	SART1	GRCh38.p7	11:65961839	GGACGACGGCGGCGG[C/T]CGGCACCGGGGGTGC	9092
rs578199352	snp	C/G	0.000399281	0.0141238	intron-variant	SART1	GRCh38.p7	11:65974036	CAGCCCCAGGGAGAG[C/G]GACATGGGTGTGTGT	9092
rs578241739	snp	A/G	0.000297265	0.0121879	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	SART1	GRCh38.p7	11:65961945	CGAACGACGGAAGCG[A/G]AGCCGGGAACGTGGG	9092
rs745400225	snp	A/G	1.84201e-05	0.00303475	upstream-variant-2KB, missense	SART1, TSGA10IP	GRCh38.p7	11:65959927	CCAGCCTGGACCCGG[A/G]GTGCAGTCCCTGAGA	9092
rs745400660	snp	C/T			upstream-variant-2KB	SART1	GRCh38.p7	11:65961510	AGTTCTGGGATCCCA[C/T]CTCCGGGTTAATTCC	9092
rs745463840	snp	C/T	3.30841e-05	0.00406706	intron-variant	SART1	GRCh38.p7	11:65977723	CGGGACCACAGCAGG[C/T]GGCAGCTCCTCACAC	9092
rs745479681	snp	A/G	1.65897e-05	0.00288003	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65965984	TTACCCTCAAGGACA[A/G]AGGTAATGCGAGCTG	9092
rs745513632	in-del	-/AAGCATGAAT			upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime	SART1, TSGA10IP	GRCh38.p7	11:65960218	GGGTCCTATAAATTC[-/AAGCATGAAT]AAGATGAAATGACTC	9092
rs745609696	snp	C/G/T	8.51584e-05	0.00652479	intron-variant	SART1	GRCh38.p7	11:65965685	GAAGTCCTAGGTCAC[C/G/T]CCTCCCTGTCCCGTA	9092
rs745658711	snp	A/G	1.68264e-05	0.0029005	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65977823	TCACACAGGACTTCA[A/G]GGAGAAGGACGGCTA	9092
rs745755363	snp	C/G/T	0.000387612	0.013917	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65966435	TGGAGCAGGGCGGCA[C/G/T]GGCTGATGGCCTGCG	9092
rs745800832	snp	C/T			intron-variant	SART1	GRCh38.p7	11:65976275	AGATAGCAGCTGGGC[C/T]TGCATGGGCTGTGGG	9092
rs745803411	in-del	-/A	1.66302e-05	0.00288355	frameshift-variant, nc-transcript-variant	SART1	GRCh38.p7	11:65977569	ATCCCTAGGGCTGCT[-/A]GGAGACCACAGTGCA	9092
rs745841160	snp	C/T	1.66629e-05	0.00288638	intron-variant, nc-transcript-variant	SART1	GRCh38.p7	11:65976383	TTTGCCCACAGCCGC[C/T]CCCTCCCCCAGGTGG	9092
rs745843357	in-del	-/T			intron-variant	SART1	GRCh38.p7	11:65972586	CAAGACCACCCCCCC[-/T]ACCAACCCCATCTCT	9092
rs745866604	snp	G/T	1.66181e-05	0.00288249	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65966388	CAAGTATGACGAAGA[G/T]CTTGAAGGGGAGCGG	9092
rs745899718	snp	C/T			intron-variant	SART1	GRCh38.p7	11:65972218	TGAAATTGGATAAAG[C/T]AGGGGCATTGTGGCA	9092
rs745929322	snp	A/G	1.6896e-05	0.0029065	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65967516	CGAAGTGGAGGAGGA[A/G]AAGGAGCCTGTGCCT	9092
rs745951916	snp	A/G	5.07447e-05	0.00503684	intron-variant	SART1	GRCh38.p7	11:65977107	CAGAACAAAGGTAGG[A/G]AGCTCAGGGCAGCCA	9092
rs745952598	snp	C/G			upstream-variant-2KB, downstream-variant-500B	SART1, TSGA10IP	GRCh38.p7	11:65960827	CCAGGGATACACTGA[C/G]GCCCATGTGGAGCTC	9092
rs746052994	snp	C/T	1.6519e-05	0.00287388	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65965902	GACCTGTACAGTGCC[C/T]GGGACCTGCAGGGCC	9092
rs746148366	snp	C/T	1.78166e-05	0.00298462	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65967567	CACCCGAGTGGAGAA[C/T]ATGGACATCAGTGAT	9092
rs746186164	snp	A/G	4.78538e-05	0.00489128	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65978689	GCTGGACGAGGAGGC[A/G]GTGGGTGCCCTTGGG	9092
rs746249050	snp	A/G	1.7586e-05	0.00296524	missense, utr-variant-5-prime, nc-transcript-variant	SART1	GRCh38.p7	11:65965115	ACCAAGGAGGAGCCC[A/G]TGACAGCTGATGTCA	9092
rs746443482	snp	G/T	1.74336e-05	0.00295237	intron-variant	SART1	GRCh38.p7	11:65965224	AAAAGCTGGGGTGAG[G/T]GGTCCTGGCCAGGGC	9092
rs746488637	snp	A/G	3.47029e-05	0.00416537	intron-variant	SART1	GRCh38.p7	11:65976629	GCTGGCTGGGGCCTG[A/G]GCCGACCCTGGTCTT	9092
rs746625714	snp	G/T			utr-variant-3-prime, downstream-variant-500B	SART1	GRCh38.p7	11:65979720	GCCCAGGATACTGGT[G/T]CCTGGCCCCACGTAC	9092
rs746632000	snp	A/T			upstream-variant-2KB	SART1	GRCh38.p7	11:65961412	TAGTGAACACCCCGT[A/T]GCCGGTGAAGTGCAA	9092
rs746679123	snp	G/T	3.54799e-05	0.00421173	intron-variant	SART1	GRCh38.p7	11:65966595	TCGGGGTCAAGATTC[G/T]CCCTCCCTCTGGGGC	9092
rs746701382	snp	A/G	1.72302e-05	0.0029351	upstream-variant-2KB, missense	SART1, TSGA10IP	GRCh38.p7	11:65959818	TCTGTGTCTTGAAGG[A/G]GCCACAGGTCAATGG	9092
rs746756126	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65970570	GAGGGCACAGCAGCT[A/G]TGGGTGACCTTGTTT	9092
rs746809193	snp	C/T	1.69006e-05	0.00290689	intron-variant, missense	SART1	GRCh38.p7	11:65964056	TCAGCTCCTGAGCCA[C/T]GCTTCTTCTTGTTCC	9092
rs746829091	in-del	-/AGA			intron-variant	SART1	GRCh38.p7	11:65973853	TACAAAACAAATCAC[-/AGA]AGAGTCATACAGTGT	9092
rs746902054	snp	C/G	1.66554e-05	0.00288573	intron-variant	SART1	GRCh38.p7	11:65966325	GAGCCAGCCTGGGTC[C/G]CAACCTGTACCTCTT	9092
rs746904339	snp	A/G	1.82824e-05	0.00302338	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65967731	GCTGGAGGAGGACGA[A/G]GCGGAGCTGGAGCTG	9092
rs746994111	snp	C/T	3.37018e-05	0.00410485	intron-variant	SART1	GRCh38.p7	11:65967676	CCCCTGTGTTTCCCC[C/T]AGAGGAAGGTGGAGC	9092
rs746996626	snp	C/T			intron-variant	SART1	GRCh38.p7	11:65974851	CCATCCAGGCTAGTA[C/T]GGTGAAACCCCATCT	9092
rs747012198	in-del	-/CA	2.89105e-05	0.0038019	intron-variant	SART1	GRCh38.p7	11:65965323	GGGCTCCTTGAGCAT[-/CA]CTTTTTCCCCTCTTC	9092
rs747100370	snp	A/G	3.75926e-05	0.00433531	intron-variant	SART1	GRCh38.p7	11:65965469	ACCTGGGCAGCATGG[A/G]GTGGTCGCCTAGTGC	9092
rs747154702	in-del	-/G	6.36345e-05	0.00564032	intron-variant	SART1	GRCh38.p7	11:65976784	GAGGGCCGCGCCGCT[-/G]GGGGGTGGGCGTTTG	9092
rs747212737	snp	A/G	8.02214e-05	0.00633279	missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	SART1	GRCh38.p7	11:65961905	AACACAAGCACCGGA[A/G]TGGCGGCAGTGGCGG	9092
rs747305007	snp	C/G	2.00282e-05	0.00316445	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	SART1	GRCh38.p7	11:65961769	AGCCGGGCTCGGAGT[C/G]GACGTGCCACTATGG	9092
rs747305088	snp	C/T	1.68363e-05	0.00290136	intron-variant	SART1	GRCh38.p7	11:65965697	CACCCCTCCCTGTCC[C/T]GTAGGCCAAGTTACT	9092
rs747305943	snp	A/G	8.41036e-05	0.00648419	intron-variant	SART1	GRCh38.p7	11:65976998	CTGCTAACCACCCCC[A/G]CCACGTGTCCCGTAG	9092
rs747360501	snp	C/T	1.72853e-05	0.00293979	stop-gained, nc-transcript-variant	SART1	GRCh38.p7	11:65967556	CCGTCGGACGACACC[C/T]GAGTGGAGAACATGG	9092
rs747412325	snp	C/T			intron-variant	SART1	GRCh38.p7	11:65963628	CTGGGATTACAGGTG[C/T]GCACCACCGTGCCTG	9092
rs747454857	snp	A/G	0.000156482	0.00884402	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65978677	GCGGATGAAGAAGCT[A/G]GACGAGGAGGCGGTG	9092
rs747485190	snp	C/G	1.71956e-05	0.00293215	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65976568	GCAGGAGGAGCTCAT[C/G]GTGCGTCTGGGGCGG	9092
rs747501811	snp	A/G	1.77922e-05	0.00298258	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	SART1	GRCh38.p7	11:65965108	GGCGGGCACCAAGGA[A/G]GAGCCCGTGACAGCT	9092
rs747555166	snp	A/C	1.6681e-05	0.00288794	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65966168	CTGCGGAAGAAGAAG[A/C]CTGACTACCTGCCCT	9092
rs747611577	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65978351	CCCAGCCCCTGCGTG[A/G]CAGGTCTCCAGGTTC	9092
rs747693158	snp	C/G	0.000195349	0.0098811	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65976427	GAAGCTGGAGTCTCG[C/G]CAGCGGGGCTGGGAG	9092
rs747755266	snp	A/G	2.56289e-05	0.00357963	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65966522	GCACAGTGGGGCCCC[A/G]GCTGGCCTCCGAATA	9092
rs747806785	snp	C/G	1.73736e-05	0.00294729	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65976547	GCTGGCTGGCAATCG[C/G]GAGGAGCAGGAGGAG	9092
rs747859677	snp	A/T			intron-variant	SART1	GRCh38.p7	11:65973221	GTTTTTTGTTTTTTT[A/T]CAAAACATACCATGA	9092
rs747866290	snp	A/C	1.86761e-05	0.00305576	intron-variant, utr-variant-5-prime	SART1	GRCh38.p7	11:65965082	CCTCACGTCTGGGCC[A/C]CCCTTCCAGAGGCGG	9092
rs747945769	snp	C/G	1.66596e-05	0.00288609	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65965714	TAGGCCAAGTTACTG[C/G]AGGAGATGGACCAAG	9092
rs747964570	snp	A/G	1.85084e-05	0.00304202	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65967577	GAGAACATGGACATC[A/G]GTGATGAGGGTGAGG	9092
rs748034473	snp	C/G/T	5.03287e-05	0.0050162	intron-variant	SART1	GRCh38.p7	11:65977548	TTGGGAGTCTCACAA[C/G/T]CCCTCCATCCCTAGG	9092
rs748116169	snp	C/T	1.70752e-05	0.00292187	intron-variant	SART1	GRCh38.p7	11:65977123	AGCTCAGGGCAGCCA[C/T]GACTTGGGTGGGCTT	9092
rs748149986	snp	A/G	1.66029e-05	0.00288117	intron-variant	SART1	GRCh38.p7	11:65965800	GCTGCAGCAGGGGTG[A/G]TACAGGGGACACTGG	9092
rs748162234	snp	A/T			utr-variant-3-prime	SART1	GRCh38.p7	11:65980120	TGTCTCAAAAAAAAT[A/T]AAAAAAATTTAAAAT	9092
rs748182321	snp	A/G	0.0001924	0.00980628	missense, utr-variant-5-prime, nc-transcript-variant	SART1	GRCh38.p7	11:65962007	AAGCTGAGGCCCGGA[A/G]CAGCACGCACGGGCG	9092
rs748251289	snp	A/C/T	0.000149495	0.0086446	missense, synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65966382	CCTGTCCAAGTATGA[A/C/T]GAAGAGCTTGAAGGG	9092
rs748385244	in-del	-/A	1.65463e-05	0.00287626	intron-variant	SART1	GRCh38.p7	11:65964494	TTAATAGCCCCTAAC[-/A]CTTGTATCTCTTGTT	9092
rs748445014	snp	A/G	1.65704e-05	0.00287836	intron-variant	SART1	GRCh38.p7	11:65967425	AGATGGCTGGGCTGG[A/G]GTGGCCTGGGGACCG	9092
rs748499624	snp	A/C/T	0.000101354	0.00711812	intron-variant	SART1	GRCh38.p7	11:65976994	TGGCCTGCTAACCAC[A/C/T]CCCGCCACGTGTCCC	9092
rs748638105	snp	C/T	6.71321e-05	0.00579323	intron-variant	SART1	GRCh38.p7	11:65966069	CACTGCTCTGTGCTG[C/T]CCCCAGGCGTGCTGC	9092
rs748704380	snp	C/T			intron-variant	SART1	GRCh38.p7	11:65964778	GTGGCCGTCGCATAC[C/T]CACTCTGGCTGTGAG	9092
rs748765198	snp	A/G	1.65408e-05	0.00287578	intron-variant	SART1	GRCh38.p7	11:65977740	GCAGCTCCTCACACT[A/G]AGGCCTCCTCTGTCT	9092
rs748795257	snp	C/T			intron-variant	SART1	GRCh38.p7	11:65977427	TGCATCTTTGCTTTG[C/T]CTGTAGAACAGGCCT	9092
rs748869636	snp	G/T	2.29888e-05	0.00339026	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65976422	GTGAAGAAGCTGGAG[G/T]CTCGCCAGCGGGGCT	9092
rs748925795	snp	A/G	1.6593e-05	0.00288031	intron-variant	SART1	GRCh38.p7	11:65964612	TGGGGGAAAGAGGCC[A/G]TCTGAAGGGGTCTTT	9092
rs748958097	snp	A/G	1.65518e-05	0.00287674	intron-variant	SART1	GRCh38.p7	11:65964485	CCTGTGTCTTTAATA[A/G]CCCCTAACACTTGTA	9092
rs749098907	snp	A/G/T	6.74802e-05	0.00580829	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65966437	GAGCAGGGCGGCACG[A/G/T]CTGATGGCCTGCGGG	9092
rs749110806	snp	C/T			intron-variant	SART1	GRCh38.p7	11:65977237	TCCGGCCCAGAGCCA[C/T]TCCTTCCCCTCCACT	9092
rs749134694	snp	A/G	1.67192e-05	0.00289125	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65965705	CCTGTCCCGTAGGCC[A/G]AGTTACTGGAGGAGA	9092
rs749179620	snp	C/T			utr-variant-3-prime, nc-transcript-variant	SART1	GRCh38.p7	11:65979080	CATATTAAATAAAGC[C/T]CCCTCCTTATTTTTT	9092
rs749230095	in-del	-/T			upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime	SART1, TSGA10IP	GRCh38.p7	11:65960410	TTGTGTGCACTGCGC[-/T]TTTTTTTTTTTTTTT	9092
rs749265550	snp	G/T	1.65567e-05	0.00287716	intron-variant	SART1	GRCh38.p7	11:65979008	CCCCTGTTCTTCTCT[G/T]CAGGAACACCATCAC	9092
rs749292430	snp	C/T	0.000109812	0.00740903	intron-variant	SART1	GRCh38.p7	11:65965499	CTTCTGGTGGCCTGA[C/T]GGCACTGAGGCGGGG	9092
rs749334887	snp	A/G			missense, nc-transcript-variant	SART1	GRCh38.p7	11:65967772	TGGAGAAGGGACGCC[A/G]GCTGCGACAGTTACA	9092
rs749368512	snp	C/T	1.66899e-05	0.00288871	intron-variant	SART1	GRCh38.p7	11:65967661	GGTCTGAGCAGGCAT[C/T]CCCTGTGTTTCCCCC	9092
rs749419049	snp	A/G	3.32193e-05	0.00407536	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65966365	CAAAAACCTCGCTCT[A/G]TCCTGTCCAAGTATG	9092
rs749492790	in-del	-/AT			intron-variant	SART1	GRCh38.p7	11:65970042	GAAGGTTTTTTAAAC[-/AT]ATGAGCCACACCCCA	9092
rs749511499	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65972326	TGGGAAGAGTCGCTC[A/G]TCAGTGCAGCGAGTG	9092
rs749551396	snp	A/G	1.76434e-05	0.00297008	intron-variant	SART1	GRCh38.p7	11:65978722	TGTGGGGGGCCCTGT[A/G]CCTGCCGGGGCAGGG	9092
rs749558210	snp	C/T			upstream-variant-2KB	SART1	GRCh38.p7	11:65961044	ATCTACAAAAAAATA[C/T]AAAAATTAAAGGGGC	9092
rs749561285	snp	A/T	3.34068e-05	0.00408684	intron-variant	SART1	GRCh38.p7	11:65966308	GCTCAGTGGCTTTTC[A/T]GGAGCCAGCCTGGGT	9092
rs749607149	snp	C/T	3.49895e-05	0.00418253	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65976706	TGGCTCCGAATCTGA[C/T]GGGGAGGAGAACATC	9092
rs749615394	snp	C/T	3.69297e-05	0.00429691	intron-variant	SART1	GRCh38.p7	11:65965330	TTGAGCATCACTTTT[C/T]CCCCTCTTCAGGAAG	9092
rs749616235	snp	C/T			downstream-variant-500B	SART1	GRCh38.p7	11:65980525	CTGTAATCCCAGCAC[C/T]CTGGGAGGCTGAGGT	9092
rs749655109	snp	C/T	1.66554e-05	0.00288573	upstream-variant-2KB, missense	SART1, TSGA10IP	GRCh38.p7	11:65959848	GGGGTGAGAATGGAG[C/T]ACTCTCCTCAGAGGC	9092
rs749775864	snp	C/G	1.65168e-05	0.00287369	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65965908	TACAGTGCCCGGGAC[C/G]TGCAGGGCCTCACCG	9092
rs749863802	snp	A/G	1.64939e-05	0.0028717	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65967312	CCGCAAGAAGGAGAA[A/G]GAGGTAGTAGTGCGG	9092
rs749871107	in-del	-/T	3.32425e-05	0.00407678	intron-variant	SART1	GRCh38.p7	11:65978767	GGCCTGCTGCAGCCC[-/T]TTTCTGAGTGGCCCC	9092
rs749889003	snp	C/T	6.04552e-05	0.00549763	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	SART1	GRCh38.p7	11:65961745	TTTGCGTTGTCTGGG[C/T]TCGGCGGCAGCCGGG	9092
rs749937405	snp	C/T	0.000117862	0.00767575	intron-variant	SART1	GRCh38.p7	11:65976780	ATGTGAGGGCCGCGC[C/T]GCTGGGGGGTGGGCG	9092
rs749963270	snp	A/G	5.63873e-05	0.00530947	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65965397	GACACTGCAGCCTGG[A/G]TCGAGAGGAGCCGGC	9092
rs750051780	snp	C/T	1.67063e-05	0.00289014	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65967472	CCTCCTTCCCTCAGA[C/T]TGCGGGGACGGGGTC	9092
rs750068965	snp	C/T			intron-variant	SART1	GRCh38.p7	11:65965044	GGCTCCCTCCTCTCC[C/T]CACCAGCCATGGGCG	9092
rs750143833	snp	A/G	1.65312e-05	0.00287495	intron-variant	SART1	GRCh38.p7	11:65967402	GGCTTGGACACGGTG[A/G]TGGGGCGAGATGGCT	9092
rs750187579	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65978329	AGCCCCAGCCCCAGC[A/G]TCCAGGCCCAGCCCC	9092
rs750192108	snp	A/G	1.67464e-05	0.0028936	intron-variant	SART1	GRCh38.p7	11:65966049	TGCGGACAAGTGTGA[A/G]TGGCCACTGCTCTGT	9092
rs750221012	snp	C/G			intron-variant	SART1	GRCh38.p7	11:65966787	ATGCTGCCAGCTCGT[C/G]CCTTGGATAAACCAT	9092
rs750340796	snp	C/T	4.00689e-05	0.00447581	intron-variant, utr-variant-5-prime	SART1	GRCh38.p7	11:65965058	CCCACCAGCCATGGG[C/T]GGGCATAGCCTCACG	9092
rs750371788	snp	C/T			intron-variant	SART1	GRCh38.p7	11:65977178	GGCCCCCTCCGGTCC[C/T]CTCTGCTGCCCCTTT	9092
rs750409147	snp	A/G	3.88583e-05	0.00440768	intron-variant	SART1	GRCh38.p7	11:65977923	GGCCTTTTGCAGGCG[A/G]AGGCCCGGCCTGCCA	9092
rs750567584	snp	A/G	6.50301e-05	0.00570183	intron-variant	SART1	GRCh38.p7	11:65967630	GCAGGGACAGGAGCC[A/G]CGGGTTGGAGGAGAT	9092
rs750579625	snp	A/G	1.67156e-05	0.00289093	missense, utr-variant-5-prime, nc-transcript-variant	SART1	GRCh38.p7	11:65964121	TCCTCACTCAGCATC[A/G]AGGAGACTAAGTGAG	9092
rs750727820	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65962993	TTTGGAGCGGGGGTG[A/G]GGGGAGATAGTTCAC	9092
rs750781492	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65969766	TCTCGCTCTGTCACC[A/G]GGCTGGAGTGCAGTG	9092
rs750809330	snp	C/T	1.75829e-05	0.00296498	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65967706	CTCCACCGCCGGGGT[C/T]CCCGCAGGTGCTGGA	9092
rs750817569	snp	G/T	0.000111501	0.00746581	intron-variant	SART1	GRCh38.p7	11:65964198	TGGGGCCAGCACGGG[G/T]GAGGCTTTCTCACAT	9092
rs750824341	snp	A/G	1.65165e-05	0.00287367	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65978898	GTGCTCAGCGGCAGC[A/G]GCAAGAGCATGAACG	9092
rs750902950	snp	A/C	1.66554e-05	0.00288573	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65966407	GAAGGGGAGCGGCCA[A/C]ATTCCTTCCGCTTGG	9092
rs750993563	in-del	-/GAC	2.24474e-05	0.00335011	cds-indel, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	SART1	GRCh38.p7	11:65961824	GAAGGAGGCGGCCGG[-/GAC]GACGACGGCGGCGGC	9092
rs750998542	snp	A/G	6.64452e-05	0.00576352	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65966360	TGCAGCAAAAACCTC[A/G]CTCTATCCTGTCCAA	9092
rs751034768	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65968750	GGGCCAGGGAGGCTG[A/G]AGCAGAGCAGAGAGT	9092
rs751037056	snp	C/T	1.71249e-05	0.00292612	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65965196	GCTGCCAAGGAGAAG[C/T]GCCTGCTGAACCAAA	9092
rs751041043	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65969809	CTCACTGCAACCTCC[A/G]TGTCCCGGGCTCAAG	9092
rs751041920	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65973621	AATGTGTGCGTGCCC[A/G]GGGCCCACCCCACAC	9092
rs751077055	snp	A/C	1.66172e-05	0.00288242	intron-variant	SART1	GRCh38.p7	11:65966347	GTACCTCTTGCCTTG[A/C]AGCAAAAACCTCGCT	9092
rs751126511	in-del	-/C	1.66902e-05	0.00288874	intron-variant	SART1	GRCh38.p7	11:65966313	GTGGCTTTTCAGGAG[-/C]CAGCCTGGGTCCCAA	9092
rs751261369	snp	C/T			downstream-variant-500B	SART1	GRCh38.p7	11:65980325	GAGTCTTTGGGTGCC[C/T]TTCCTTGAGCTCTGT	9092
rs751288078	snp	A/G	2.86234e-05	0.00378297	intron-variant	SART1	GRCh38.p7	11:65965317	GGAGCTGGGCTCCTT[A/G]AGCATCACTTTTTCC	9092
rs751479787	snp	A/T	1.74442e-05	0.00295327	intron-variant	SART1	GRCh38.p7	11:65964258	TGTTTAAATCATCTT[A/T]GCCAACAGTTGACTT	9092
rs751519335	snp	A/C	1.65529e-05	0.00287683	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65965961	CCGAGAAGGGGAGAC[A/C]ATGATTCTTACCCTC	9092
rs751541011	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65970946	TTCATGAGCTGAGGA[A/G]GGGGATGGTGGGATT	9092
rs751568669	snp	C/T			synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65976509	GAGTTCTGCCGCACC[C/T]TGGGGGAGATCCCCA	9092
rs751621132	snp	G/T			intron-variant	SART1	GRCh38.p7	11:65966628	CTGCCCTGCCCGCAG[G/T]CACTGAGAAGACAGG	9092
rs751664977	snp	C/G	1.67981e-05	0.00289806	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65977097	GCTCCTGTGTCAGAA[C/G]AAAGGTAGGGAGCTC	9092
rs751676782	snp	C/G/T	4.15578e-05	0.00455823	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65966501	GGCTGCAGGCTCAGT[C/G/T]CCTGAGCACAGTGGG	9092
rs751749145	snp	C/T	1.66679e-05	0.00288681	utr-variant-3-prime, nc-transcript-variant	SART1	GRCh38.p7	11:65979061	CCGGCCCTGCCTCAA[C/T]CTTCATATTAAATAA	9092
rs751916630	snp	C/T	1.67008e-05	0.00288965	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	SART1	GRCh38.p7	11:65964117	TGCCTCCTCACTCAG[C/T]ATCGAGGAGACTAAG	9092
rs751938796	snp	A/C/G	6.80855e-05	0.00583428	intron-variant	SART1	GRCh38.p7	11:65977527	GGAGCTGTGGCTCTC[A/C/G]AGGGGTTGGGAGTCT	9092
rs752004691	snp	G/T	1.67998e-05	0.00289821	intron-variant	SART1	GRCh38.p7	11:65963991	GGTGAGGGGCCCTCA[G/T]TTTTGTTCCTGCAGC	9092
rs752006635	snp	G/T	1.65446e-05	0.00287612	intron-variant	SART1	GRCh38.p7	11:65965837	TGCTACCGGAATCCC[G/T]AGGTTGGGTGCGTGG	9092
rs752014238	snp	A/G	3.36327e-05	0.00410063	intron-variant	SART1	GRCh38.p7	11:65966266	GAGGTGGAGAATGTC[A/G]GGAATGGGGGCTCTG	9092
rs752099824	snp	C/T	2.41595e-05	0.00347551	intron-variant	SART1	GRCh38.p7	11:65967607	GGCCCGGCCAGGGGG[C/T]GGGAGGGGCAGGGAC	9092
rs752146577	snp	A/T			intron-variant	SART1	GRCh38.p7	11:65971996	TGACTCTATCTCAGC[A/T]CACTGCAATTTCCAC	9092
rs752152298	snp	C/T	1.66944e-05	0.0028891	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65966153	GAGAAAAATGTGGAG[C/T]TGCGGAAGAAGAAGC	9092
rs752252500	snp	G/T	8.47594e-05	0.00650942	intron-variant	SART1	GRCh38.p7	11:65978746	GGCAGGGGTGGCTGG[G/T]GTGTGGGGCCTGCTG	9092
rs752256921	snp	A/G	9.50367e-05	0.0068927	intron-variant	SART1	GRCh38.p7	11:65967601	GGTGAGGGCCCGGCC[A/G]GGGGGTGGGAGGGGC	9092
rs752378401	snp	C/G	1.706e-05	0.00292057	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65965168	GCGAGAGGAGCTGCG[C/G]GAGAAGCTGGCGGCT	9092
rs752382856	in-del	-/A	5.33841e-05	0.00516616	upstream-variant-2KB, utr-variant-3-prime	SART1, TSGA10IP	GRCh38.p7	11:65959943	TGCAGTCCCTGAGAT[-/A]AAAATTAAAGGCTTT	9092
rs752447113	snp	C/T	4.21026e-05	0.00458798	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65978663	ATGAAGACAGAGCGG[C/T]GGATGAAGAAGCTGG	9092
rs752486913	snp	A/C	2.32312e-05	0.00340809	upstream-variant-2KB, missense	SART1, TSGA10IP	GRCh38.p7	11:65959890	GAACCCACCGGCAGC[A/C]AGCCTGACAGGCACT	9092
rs752503125	snp	C/T			upstream-variant-2KB	SART1	GRCh38.p7	11:65961317	CTCGGGAAAACAACA[C/T]CCGTTGGAGCCACGA	9092
rs752572715	snp	G/T	5.51207e-05	0.00524951	intron-variant	SART1	GRCh38.p7	11:65965309	GGGGAGCAGGAGCTG[G/T]GCTCCTTGAGCATCA	9092
rs752574700	snp	A/G	9.85561e-05	0.00701914	upstream-variant-2KB, intron-variant	SART1, TSGA10IP	GRCh38.p7	11:65959802	GAGTCAGGGGCCTCT[A/G]TCTGTGTCTTGAAGG	9092
rs752608781	snp	A/G	1.64966e-05	0.00287194	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65967356	TGCCTCTCGGGGACC[A/G]GACTCAGGATGGGGA	9092
rs752671197	snp	A/G/T	2.54398e-05	0.00356641	intron-variant	SART1	GRCh38.p7	11:65964190	GGTGGCTCTGGGGCC[A/G/T]GCACGGGGGAGGCTT	9092
rs752704126	snp	C/T	0.000150288	0.00866725	intron-variant	SART1	GRCh38.p7	11:65977911	GGAGGTGAGCAGGGC[C/T]TTTTGCAGGCGGAGG	9092
rs752809474	snp	A/G	1.65436e-05	0.00287602	intron-variant	SART1	GRCh38.p7	11:65964585	GGTGAGTATGGGGCT[A/G]AGGATAGGGTTTGGG	9092
rs752827451	snp	C/G			intron-variant	SART1	GRCh38.p7	11:65965254	CAGGCAAGGGAAGGG[C/G]TGGGGAGGCCACCAT	9092
rs752838323	snp	C/T	6.07736e-05	0.00551209	intron-variant	SART1	GRCh38.p7	11:65976353	CTCAATGGCATCACC[C/T]CAGAAACTGCTGGGT	9092
rs752902172	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65976128	GGGGCTTTGGAGGGG[A/G]ATTGGCACAGGCCTG	9092
rs752920104	snp	C/G	1.85029e-05	0.00304157	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65966477	TGGAGGAGATCCGGG[C/G]CAAGCTGCGGCTGCA	9092
rs753006304	snp	A/G	1.83586e-05	0.00302968	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65976476	CGGAAGGGGGCCATC[A/G]TGTTCAACGCCACGT	9092
rs753024076	in-del	-/T	0.000143702	0.00847529	intron-variant	SART1	GRCh38.p7	11:65967668	CAGGCATCCCCTGTG[-/T]TTTCCCCCAGAGGAA	9092
rs753034632	snp	C/T	5.03943e-05	0.00501942	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65966430	CCGCTTGGAGCAGGG[C/T]GGCACGGCTGATGGC	9092
rs753050424	snp	C/T	1.66441e-05	0.00288474	utr-variant-3-prime, nc-transcript-variant	SART1	GRCh38.p7	11:65979051	CCCTCCCGCCCCGGC[C/T]CTGCCTCAACCTTCA	9092
rs753116992	snp	A/G	0.000152474	0.00873005	intron-variant	SART1	GRCh38.p7	11:65962140	TCGGGCGGGGGTCCC[A/G]GAACGCGTGGGTCTG	9092
rs753154851	snp	G/T	1.70371e-05	0.0029186	intron-variant	SART1	GRCh38.p7	11:65977515	TCAGGCGGCCCTGGA[G/T]CTGTGGCTCTCGAGG	9092
rs753303090	snp	C/T			intron-variant	SART1	GRCh38.p7	11:65978457	GCCAGCGTCTGTGCT[C/T]TTTTCCCATCCCCTT	9092
rs753307748	snp	A/G	3.9748e-05	0.00445785	missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	SART1	GRCh38.p7	11:65961880	CCGCCGCGGCACCGG[A/G]AACACAAAAAACACA	9092
rs753324704	snp	C/T			upstream-variant-2KB	SART1	GRCh38.p7	11:65961676	ACGGAAGCAGCCGCT[C/T]TTAGTTTCCGGCAAC	9092
rs753365931	snp	C/T	3.38587e-05	0.00411439	missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	SART1	GRCh38.p7	11:65961869	CCACCGAGCAGCCGC[C/T]GCGGCACCGGGAACA	9092
rs753405686	snp	C/T	1.65559e-05	0.00287709	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65977055	GGACGAGGAACCGAT[C/T]GTGAATAGGGGGCTG	9092
rs753418902	snp	A/G	0.000290559	0.0120497	intron-variant	SART1	GRCh38.p7	11:65977930	TGCAGGCGGAGGCCC[A/G]GCCTGCCACAGGGAG	9092
rs753516401	snp	C/T	6.68662e-05	0.00578175	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65966132	CTGGTGGATAAGGAG[C/T]GGGCAGAGAAAAATG	9092
rs753565000	snp	C/T	6.94227e-05	0.00589123	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65978629	GTCGCACCGCTTCCA[C/T]GGCAAGGGCTCAGGC	9092
rs753579629	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65968459	TGTGTGGGGGAGAGC[A/G]TGGGGAGCAGCAGTG	9092
rs753596635	snp	C/T	3.41752e-05	0.00413357	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65967545	CTCAGCCCCTGCCGT[C/T]GGACGACACCCGAGT	9092
rs753610379	snp	C/T	1.67559e-05	0.00289442	intron-variant	SART1	GRCh38.p7	11:65966054	ACAAGTGTGAATGGC[C/T]ACTGCTCTGTGCTGC	9092
rs753645237	snp	C/T	3.3539e-05	0.00409492	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65967481	CTCAGACTGCGGGGA[C/T]GGGGTCGCCGCCGAG	9092
rs753713658	snp	C/T	3.83951e-05	0.00438133	intron-variant, utr-variant-5-prime	SART1	GRCh38.p7	11:65965072	GCGGGCATAGCCTCA[C/T]GTCTGGGCCCCCCTT	9092
rs753729024	snp	C/T	3.43578e-05	0.0041446	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65976670	GGACTTTGAACGGGA[C/T]GAGGAGCGCTCAGCC	9092
rs753799792	snp	C/T	4.15377e-05	0.0045571	intron-variant	SART1	GRCh38.p7	11:65964224	CACATGAAAGTGTGC[C/T]AATCAGAGTTGGAAA	9092
rs753805421	snp	C/T	0.000106536	0.00729771	upstream-variant-2KB, intron-variant	SART1, TSGA10IP	GRCh38.p7	11:65959768	AGTGGTTTCCTTGGG[C/T]ATGGGGGTGGGAGCT	9092
rs753894188	snp	A/G			utr-variant-3-prime, downstream-variant-500B	SART1	GRCh38.p7	11:65979383	CCTGTAATGTCTCCC[A/G]GTCAGGGCAGCCCAG	9092
rs753922669	snp	C/T			intron-variant	SART1	GRCh38.p7	11:65973909	TACACAACAAAATAA[C/T]TGTTCAGGGGCAGGT	9092
rs753948472	snp	A/C	3.30682e-05	0.00406608	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65965942	AGCATGCCATTGATT[A/C]CTTCCGAGAAGGGGA	9092
rs753979397	snp	C/G	1.6916e-05	0.00290822	intron-variant	SART1	GRCh38.p7	11:65964139	GAGACTAAGTGAGTA[C/G]TGTCTCCCTTGTTTC	9092
rs754066795	snp	A/C	3.15273e-05	0.00397022	intron-variant	SART1	GRCh38.p7	11:65967861	ACTGCGTCAGCAGTC[A/C]CCTGTCCTCACGAGC	9092
rs754154608	snp	G/T	1.65671e-05	0.00287807	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65977784	TCGATGACAAGTACA[G/T]CCGGAGGGAGGAATA	9092
rs754194384	snp	A/G	1.65534e-05	0.00287688	intron-variant	SART1	GRCh38.p7	11:65978922	ATGAACGCGTGAGTG[A/G]CTCGAGGCTGGTGGG	9092
rs754213674	snp	C/T			intron-variant	SART1	GRCh38.p7	11:65972445	AAAAACTTCACATTT[C/T]GGAATCAAATTAAGG	9092
rs754233385	snp	A/G/T	5.00909e-05	0.00500433	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65966417	GGCCACATTCCTTCC[A/G/T]CTTGGAGCAGGGCGG	9092
rs754262463	snp	C/G	1.70755e-05	0.00292189	intron-variant	SART1	GRCh38.p7	11:65976985	GAGCCGGTATGGCCT[C/G]CTAACCACCCCCGCC	9092
rs754266437	in-del	-/T	3.80409e-05	0.00436108	intron-variant	SART1	GRCh38.p7	11:65964221	TCTCACATGAAAGTG[-/T]GCTAATCAGAGTTGG	9092
rs754283294	in-del	-/GGA	8.42893e-05	0.00649134	cds-indel, nc-transcript-variant	SART1	GRCh38.p7	11:65967506	CCGAGTGTCCGAAGT[-/GGA]GGAGGAGGAGAAGGA	9092
rs754358785	snp	A/G	1.75894e-05	0.00296553	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65966463	GCGGGAGCGGGAGCT[A/G]GAGGAGATCCGGGCC	9092
rs754417775	snp	A/C/G	0.000170892	0.00924222	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65967546	TCAGCCCCTGCCGTC[A/C/G]GACGACACCCGAGTG	9092
rs754425810	snp	C/T	0.000207204	0.0101764	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65965409	TGGATCGAGAGGAGC[C/T]GGCAGCTGCAGAAGG	9092
rs754453038	snp	A/C			intron-variant, missense	SART1	GRCh38.p7	11:65964070	ATGCTTCTTCTTGTT[A/C]CAGCTGCCAGCTCCA	9092
rs754502457	snp	A/G	1.67506e-05	0.00289396	intron-variant	SART1	GRCh38.p7	11:65966055	CAAGTGTGAATGGCC[A/G]CTGCTCTGTGCTGCC	9092
rs754512727	snp	C/T			intron-variant	SART1	GRCh38.p7	11:65967124	AGTAACCACCCCACA[C/T]GTTGCTCATGTGTGG	9092
rs754595145	snp	C/T			upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime	SART1, TSGA10IP	GRCh38.p7	11:65960345	CCACACAGGGAGCCA[C/T]AGACTGAGCAACCAC	9092
rs754597795	snp	C/G	0.00311371	0.0393339	intron-variant	SART1	GRCh38.p7	11:65977931	GCAGGCGGAGGCCCG[C/G]CCTGCCACAGGGAGG	9092
rs754610860	snp	C/T			intron-variant	SART1	GRCh38.p7	11:65978200	CTGGCTTTCCTGGCC[C/T]GCAGGGCCATTCCAG	9092
rs754650221	snp	C/G			utr-variant-5-prime, upstream-variant-2KB	SART1	GRCh38.p7	11:65961699	CCGGCAACACGACAG[C/G]GGCTGCCGAGCGACC	9092
rs754848900	snp	A/T	1.66004e-05	0.00288096	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65967262	TCTTCCCTTAAGGTG[A/T]CCTTTAAAAAGACCA	9092
rs754872648	snp	A/C/T	0.000137955	0.00830432	synonymous-codon, missense, nc-transcript-variant	SART1	GRCh38.p7	11:65978660	AAGATGAAGACAGAG[A/C/T]GGCGGATGAAGAAGC	9092
rs754894158	snp	C/T	5.05174e-05	0.00502555	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65967501	TCGCCGCCGAGTGTC[C/T]GAAGTGGAGGAGGAG	9092
rs754910396	snp	A/T	4.04523e-05	0.00449716	upstream-variant-2KB, intron-variant	SART1, TSGA10IP	GRCh38.p7	11:65959776	CCTTGGGCATGGGGG[A/T]GGGAGCTGCAGAGTC	9092
rs754935730	snp	A/G	0.000114318	0.00755951	intron-variant	SART1	GRCh38.p7	11:65966569	ATGGTGAGCCCTCCC[A/G]TGCCTTATACTCGGG	9092
rs754952771	snp	C/T	0.000134528	0.00820037	utr-variant-3-prime, nc-transcript-variant	SART1	GRCh38.p7	11:65979081	ATATTAAATAAAGCT[C/T]CCTCCTTATTTTTTC	9092
rs755048162	snp	A/G	0.000867331	0.0208066	intron-variant	SART1	GRCh38.p7	11:65964250	GGAAAGATTGTTTAA[A/G]TCATCTTAGCCAACA	9092
rs755049031	snp	C/T			intron-variant	SART1	GRCh38.p7	11:65963213	AGGAGACAGAGTAAC[C/T]AAAAAGGCAGGAAAA	9092
rs755089739	snp	C/T	9.29325e-05	0.00681598	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65967728	GGTGCTGGAGGAGGA[C/T]GAGGCGGAGCTGGAG	9092
rs755284027	snp	C/T	0.00033151	0.0128703	intron-variant	SART1	GRCh38.p7	11:65967872	AGTCACCTGTCCTCA[C/T]GAGCACCTGTGTCAT	9092
rs755287286	snp	C/T	1.66153e-05	0.00288225	intron-variant	SART1	GRCh38.p7	11:65978983	CTGTGCCCGCCTCTG[C/T]AGCCTCACGCCCCTG	9092
rs755328237	in-del	-/C	3.96613e-05	0.00445298	intron-variant	SART1	GRCh38.p7	11:65964223	TCACATGAAAGTGTG[-/C]TAATCAGAGTTGGAA	9092
rs755379030	snp	C/T	3.31192e-05	0.00406921	intron-variant	SART1	GRCh38.p7	11:65978925	AACGCGTGAGTGGCT[C/T]GAGGCTGGTGGGGTA	9092
rs755422290	in-del	-/A	2.25706e-05	0.00335928	intron-variant	SART1	GRCh38.p7	11:65967601	GGTGAGGGCCCGGCC[-/A]GGGGGTGGGAGGGGC	9092
rs755434498	snp	C/T	3.78652e-05	0.00435099	synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	SART1	GRCh38.p7	11:65961876	GCAGCCGCCGCGGCA[C/T]CGGGAACACAAAAAA	9092
rs755518449	snp	A/C	0.000242026	0.0109979	intron-variant	SART1	GRCh38.p7	11:65976992	TATGGCCTGCTAACC[A/C]CCCCCGCCACGTGTC	9092
rs755536747	snp	A/G	2.07907e-05	0.00322411	intron-variant	SART1	GRCh38.p7	11:65964176	GTTTTTCTAAGAGAG[A/G]TGGCTCTGGGGCCAG	9092
rs755553950	snp	C/T	1.70837e-05	0.00292259	intron-variant	SART1	GRCh38.p7	11:65976979	TGAGAAGAGCCGGTA[C/T]GGCCTGCTAACCACC	9092
rs755557307	snp	A/C	1.69602e-05	0.00291201	intron-variant	SART1	GRCh38.p7	11:65965689	TCCTAGGTCACCCCT[A/C]CCTGTCCCGTAGGCC	9092
rs755607720	snp	A/G/T	6.04605e-05	0.00549793	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	SART1	GRCh38.p7	11:65961746	TTGCGTTGTCTGGGC[A/G/T]CGGCGGCAGCCGGGC	9092
rs755646184	snp	A/T			intron-variant	SART1	GRCh38.p7	11:65963307	CACATACCACAGGAG[A/T]TCAAGCAAAACCAGA	9092
rs755666445	snp	C/T	4.96381e-05	0.00498162	intron-variant	SART1	GRCh38.p7	11:65967408	GACACGGTGGTGGGG[C/T]GAGATGGCTGGGCTG	9092
rs755714375	snp	A/G	3.05946e-05	0.00391106	intron-variant	SART1	GRCh38.p7	11:65976781	TGTGAGGGCCGCGCC[A/G]CTGGGGGGTGGGCGT	9092
rs755734396	snp	C/T			intron-variant	SART1	GRCh38.p7	11:65969923	GAAACAGGGTTTCAC[C/T]GTGTTGGTCAGGCTG	9092
rs755755827	snp	C/T	1.66056e-05	0.00288141	intron-variant	SART1	GRCh38.p7	11:65965991	CAAGGACAAAGGTAA[C/T]GCGAGCTGGGTGCCC	9092
rs755772823	snp	C/T	5.02475e-05	0.00501211	intron-variant	SART1	GRCh38.p7	11:65966050	GCGGACAAGTGTGAA[C/T]GGCCACTGCTCTGTG	9092
rs755844106	snp	C/T			intron-variant	SART1	GRCh38.p7	11:65966808	GATAAACCATTTAAC[C/T]GTGAGCCTGGGGCAC	9092
rs755849447	snp	C/G	0.000373264	0.0136562	intron-variant	SART1	GRCh38.p7	11:65977926	CTTTTGCAGGCGGAG[C/G]CCCGGCCTGCCACAG	9092
rs755887180	snp	C/T	3.5517e-05	0.00421394	intron-variant, nc-transcript-variant	SART1	GRCh38.p7	11:65976392	AGCCGCTCCCTCCCC[C/T]AGGTGGTGGAGATTG	9092
rs755943045	snp	A/G	1.6972e-05	0.00291303	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65977830	GGACTTCAAGGAGAA[A/G]GACGGCTACAAACCC	9092
rs755948600	snp	A/G			utr-variant-3-prime, downstream-variant-500B	SART1	GRCh38.p7	11:65979468	CCTTCTGTCCTGGCT[A/G]TCCTGTGCCACCCTG	9092
rs756007683	snp	C/T	1.8186e-05	0.0030154	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65976489	TCGTGTTCAACGCCA[C/T]GTCCGAGTTCTGCCG	9092
rs756060421	snp	C/T			intron-variant	SART1	GRCh38.p7	11:65977202	CCCCTTTCTCTCAGT[C/T]CCAATGCTGGAGCCA	9092
rs756143107	snp	C/T	4.11582e-05	0.00453623	intron-variant, utr-variant-5-prime	SART1	GRCh38.p7	11:65964028	CAACGATGCTGGCTT[C/T]TTGGCCCTGTGTTCA	9092
rs756210175	snp	G/T	3.30797e-05	0.00406679	intron-variant	SART1	GRCh38.p7	11:65965854	GGTTGGGTGCGTGGA[G/T]GGAGGTTCCTGACTC	9092
rs756211517	snp	C/T	3.36644e-05	0.00410257	intron-variant	SART1	GRCh38.p7	11:65977541	CGAGGGGTTGGGAGT[C/T]TCACAACCCCTCCAT	9092
rs756324037	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65972988	ATCCTGGTCAACACA[A/G]TGAAACCCTGTCTCT	9092
rs756359333	snp	A/C	3.27188e-05	0.00404454	intron-variant	SART1	GRCh38.p7	11:65967631	CAGGGACAGGAGCCG[A/C]GGGTTGGAGGAGATG	9092
rs756390215	snp	C/T	1.65701e-05	0.00287833	intron-variant	SART1	GRCh38.p7	11:65978788	GAGTGGCCCCGACCC[C/T]TCAGCTCCTGAAGAA	9092
rs756398781	snp	C/T	1.66106e-05	0.00288184	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65966361	GCAGCAAAAACCTCG[C/T]TCTATCCTGTCCAAG	9092
rs756408121	snp	A/G	0.000150513	0.00867374	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	SART1	GRCh38.p7	11:65964123	CTCACTCAGCATCGA[A/G]GAGACTAAGTGAGTA	9092
rs756498608	snp	C/T	7.87371e-05	0.00627394	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65967707	TCCACCGCCGGGGTC[C/T]CCGCAGGTGCTGGAG	9092
rs756543804	snp	G/T			intron-variant	SART1	GRCh38.p7	11:65962161	CGTGGGTCTGGGTGT[G/T]CGCGCAGTGTCAGCG	9092
rs756544399	snp	A/G	1.82797e-05	0.00302316	upstream-variant-2KB, missense	SART1, TSGA10IP	GRCh38.p7	11:65959930	GCCTGGACCCGGAGT[A/G]CAGTCCCTGAGATAA	9092
rs756563602	snp	A/G	3.34426e-05	0.00408903	intron-variant	SART1	GRCh38.p7	11:65966301	GGTGGTGGCTCAGTG[A/G]CTTTTCAGGAGCCAG	9092
rs756573228	snp	C/G			intron-variant	SART1	GRCh38.p7	11:65969786	GGAGTGCAGTGGCGC[C/G]ATCTCGGCTCACTGC	9092
rs756632356	snp	A/T	3.30978e-05	0.0040679	intron-variant	SART1	GRCh38.p7	11:65965321	CTGGGCTCCTTGAGC[A/T]TCACTTTTTCCCCTC	9092
rs756661190	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65973654	CTCCCGAGTGTGCCC[A/G]TGTGCACCAGGAGAC	9092
rs756662526	in-del	-/TAAG	1.67607e-05	0.00289483	splice-donor-variant	SART1	GRCh38.p7	11:65964129	CAGCATCGAGGAGAC[-/TAAG]TGAGTACTGTCTCCC	9092
rs756664276	snp	A/T			intron-variant	SART1	GRCh38.p7	11:65963000	CGGGGGTGGGGGGAG[A/T]TAGTTCACTTTTGGG	9092
rs756777909	snp	C/T	1.72531e-05	0.00293705	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65976688	GGAGCGCTCAGCCAA[C/T]GGTGGCTCCGAATCT	9092
rs756787589	snp	C/T	5.14858e-05	0.00507348	upstream-variant-2KB, synonymous-codon	SART1, TSGA10IP	GRCh38.p7	11:65959820	TGTGTCTTGAAGGAG[C/T]CACAGGTCAATGGGG	9092
rs756808243	in-del	-/C			downstream-variant-500B	SART1	GRCh38.p7	11:65980596	CAACACGGTAAAACT[-/C]CCGTCTTTGACTAAA	9092
rs756865808	snp	C/G	1.6625e-05	0.00288309	intron-variant	SART1	GRCh38.p7	11:65978766	GGGGCCTGCTGCAGC[C/G]CTTTCTGAGTGGCCC	9092
rs756866023	snp	A/G	4.95356e-05	0.00497648	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65967285	AAAGACCAAGCGGAG[A/G]GTGAAGAAAATCCGC	9092
rs756894924	snp	G/T			intron-variant	SART1	GRCh38.p7	11:65968771	AGCAGAGAGTGAGGG[G/T]TGGCGTGAGCTGAGA	9092
rs756911090	snp	A/G	7.4279e-05	0.00609377	upstream-variant-2KB, synonymous-codon	SART1, TSGA10IP	GRCh38.p7	11:65959925	CCCCAGCCTGGACCC[A/G]GAGTGCAGTCCCTGA	9092
rs756969506	snp	A/C			upstream-variant-2KB	SART1	GRCh38.p7	11:65961481	CACTGACTTAATGGG[A/C]TCTAAGTCCTTCCAG	9092
rs756972184	snp	C/T	5.60617e-05	0.00529412	intron-variant	SART1	GRCh38.p7	11:65976777	AGGATGTGAGGGCCG[C/T]GCCGCTGGGGGGTGG	9092
rs757046857	snp	C/T	1.65556e-05	0.00287707	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65965963	GAGAAGGGGAGACAA[C/T]GATTCTTACCCTCAA	9092
rs757120155	snp	G/T	3.3089e-05	0.00406736	intron-variant	SART1	GRCh38.p7	11:65964587	TGAGTATGGGGCTGA[G/T]GATAGGGTTTGGGGG	9092
rs757124255	snp	A/T			intron-variant	SART1	GRCh38.p7	11:65974707	TATGATGCATTAGAT[A/T]TACCTCGTTTTATGT	9092
rs757154227	snp	C/G/T	3.32332e-05	0.00407624	missense, stop-gained, nc-transcript-variant	SART1	GRCh38.p7	11:65977801	CGGAGGGAGGAATAC[C/G/T]GAGGCTTCACACAGG	9092
rs757187664	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65976258	GAGTGGAGTTAGGCG[A/G]CAGATAGCAGCTGGG	9092
rs757317150	snp	C/G	5.00188e-05	0.00500069	utr-variant-3-prime, nc-transcript-variant	SART1	GRCh38.p7	11:65979062	CGGCCCTGCCTCAAC[C/G]TTCATATTAAATAAA	9092
rs757331834	snp	A/G	3.83649e-05	0.00437961	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65966556	CACGCCTGAGGAGAT[A/G]GTGAGCCCTCCCGTG	9092
rs757489418	snp	A/C			intron-variant	SART1	GRCh38.p7	11:65966645	ACTGAGAAGACAGGG[A/C]GAGTATTTGTGTTCA	9092
rs757490054	snp	C/T	8.01957e-05	0.00633178	intron-variant	SART1	GRCh38.p7	11:65964003	TCATTTTTGTTCCTG[C/T]AGCTGGAGCCAACGA	9092
rs757515432	snp	A/G	1.69115e-05	0.00290782	intron-variant	SART1	GRCh38.p7	11:65977105	GTCAGAACAAAGGTA[A/G]GGAGCTCAGGGCAGC	9092
rs757576462	snp	C/T	0.000121692	0.00779942	synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	SART1	GRCh38.p7	11:65961927	CAGTGGCGGTAGCGG[C/T]GGCGAACGACGGAAG	9092
rs757578405	snp	C/T	1.66073e-05	0.00288156	intron-variant	SART1	GRCh38.p7	11:65965792	CAGGTGAGGCTGCAG[C/T]AGGGGTGGTACAGGG	9092
rs757587464	snp	C/G			missense, utr-variant-5-prime, nc-transcript-variant	SART1	GRCh38.p7	11:65962039	GAGCGCAGCCAGGCA[C/G]AGCCCTCCGAGCGGC	9092
rs757594096	snp	A/G	5.86837e-05	0.00541649	intron-variant	SART1	GRCh38.p7	11:65967623	GGGAGGGGCAGGGAC[A/G]GGAGCCGCGGGTTGG	9092
rs757681135	snp	G/T			intron-variant	SART1	GRCh38.p7	11:65972049	ATACAGTCATTGGGG[G/T]TTAGGGCTTCCCGAT	9092
rs757706623	snp	C/T	1.6612e-05	0.00288196	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65966356	GCCTTGCAGCAAAAA[C/T]CTCGCTCTATCCTGT	9092
rs757728913	snp	A/G	3.42648e-05	0.00413899	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65965197	CTGCCAAGGAGAAGC[A/G]CCTGCTGAACCAAAA	9092
rs757738593	snp	A/G			upstream-variant-2KB, downstream-variant-500B	SART1, TSGA10IP	GRCh38.p7	11:65960722	GCACTGGGGTTTTAA[A/G]TCCCAATAGTTTTAA	9092
rs757765390	snp	C/T			intron-variant	SART1	GRCh38.p7	11:65968859	AGAGGCACAGTGGGC[C/T]GGGCACTGCTCACAT	9092
rs757796506	snp	G/T	1.68055e-05	0.0028987	intron-variant	SART1	GRCh38.p7	11:65966272	GAGAATGTCGGGAAT[G/T]GGGGCTCTGAGGAGG	9092
rs757810512	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65972938	GCACTTTGGGAGGCC[A/G]AGGCGGGCGGATCAC	9092
rs757816096	snp	A/G	1.67744e-05	0.00289602	intron-variant	SART1	GRCh38.p7	11:65966248	GGCTGGGTGGCGGGG[A/G]CTGAGGTGGAGAATG	9092
rs757854440	snp	C/T	3.00314e-05	0.00387489	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65978680	GATGAAGAAGCTGGA[C/T]GAGGAGGCGGTGGGT	9092
rs757960416	snp	G/T	2.36594e-05	0.00343935	intron-variant	SART1	GRCh38.p7	11:65967603	TGAGGGCCCGGCCAG[G/T]GGGTGGGAGGGGCAG	9092
rs757982003	snp	C/T			downstream-variant-500B	SART1	GRCh38.p7	11:65980286	CTGACACCATTACTT[C/T]TGTGCAGCGGGAGCT	9092
rs757992082	snp	G/T	0.000353288	0.0132861	intron-variant	SART1	GRCh38.p7	11:65976611	CTTCCCTCGGCTGGG[G/T]GGGCTGGCTGGGGCC	9092
rs758010416	snp	C/T	1.70566e-05	0.00292027	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65965179	TGCGGGAGAAGCTGG[C/T]GGCTGCCAAGGAGAA	9092
rs758060674	snp	C/G	9.80056e-05	0.00699951	upstream-variant-2KB, intron-variant	SART1, TSGA10IP	GRCh38.p7	11:65959804	GTCAGGGGCCTCTAT[C/G]TGTGTCTTGAAGGAG	9092
rs758064902	in-del	-/GGCTTTAT	1.76883e-05	0.00297386	upstream-variant-2KB, utr-variant-3-prime	SART1, TSGA10IP	GRCh38.p7	11:65959953	TGAGATAAAATTAAA[-/GGCTTTAT]GGCAAACACAGTATG	9092
rs758130199	snp	C/T	1.66879e-05	0.00288855	intron-variant	SART1	GRCh38.p7	11:65978756	GCTGGTGTGTGGGGC[C/T]TGCTGCAGCCCTTTC	9092
rs758135398	snp	A/G			utr-variant-3-prime	SART1	GRCh38.p7	11:65980073	GGCCCTGATTGAGCC[A/G]CCACACTGCAGCCTA	9092
rs758180449	snp	A/T	3.30945e-05	0.0040677	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65967272	AGGTGACCTTTAAAA[A/T]GACCAAGCGGAGGGT	9092
rs758244560	snp	A/G	1.7318e-05	0.00294256	intron-variant	SART1	GRCh38.p7	11:65966578	CCTCCCGTGCCTTAT[A/G]CTCGGGGTCAAGATT	9092
rs758257359	snp	C/T	2.0155e-05	0.00317444	upstream-variant-2KB, synonymous-codon	SART1, TSGA10IP	GRCh38.p7	11:65959907	GCCTGACAGGCACTA[C/T]AACCCCAGCCTGGAC	9092
rs758275106	snp	A/G	3.30819e-05	0.00406692	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65965948	CCATTGATTCCTTCC[A/G]AGAAGGGGAGACAAT	9092
rs758275486	snp	C/T			upstream-variant-2KB	SART1	GRCh38.p7	11:65961336	TTGGAGCCACGACCC[C/T]AGGAGTCCACTAAGC	9092
rs758380510	snp	C/T			intron-variant	SART1	GRCh38.p7	11:65968687	CTGGCATTTAGGCAG[C/T]AGACCAACCAGCAGG	9092
rs758474600	snp	A/G	9.72905e-05	0.00697393	intron-variant, splice-acceptor-variant	SART1	GRCh38.p7	11:65976377	GCTGGGTTTGCCCAC[A/G]GCCGCTCCCTCCCCC	9092
rs758567801	in-del	-/T			intron-variant	SART1	GRCh38.p7	11:65967950	TGTTTTCTGGGTTTG[-/T]TTTTTTTTTTTTTTT	9092
rs758636617	snp	C/G/T	0.000186169	0.00964635	intron-variant	SART1	GRCh38.p7	11:65965691	CTAGGTCACCCCTCC[C/G/T]TGTCCCGTAGGCCAA	9092
rs758644636	in-del	-/C	2.47644e-05	0.00351875	intron-variant	SART1	GRCh38.p7	11:65967827	GGCGAGAAGGTGAGG[-/C]CTGGGCATGGGCAGG	9092
rs758678327	snp	C/T			intron-variant	SART1	GRCh38.p7	11:65964275	CCAACAGTTGACTTA[C/T]AGAAGAGAAAACTAA	9092
rs758689000	snp	C/T	5.53021e-05	0.00525814	missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	SART1	GRCh38.p7	11:65961898	CACAAAAAACACAAG[C/T]ACCGGAGTGGCGGCA	9092
rs758740733	snp	A/G	5.0474e-05	0.00502339	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65967496	CGGGGTCGCCGCCGA[A/G]TGTCCGAAGTGGAGG	9092
rs758742324	snp	C/T	1.67192e-05	0.00289125	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65977086	GCAGCTGCCCTGCTC[C/T]TGTGTCAGAACAAAG	9092
rs758758531	snp	C/T	1.66454e-05	0.00288486	utr-variant-3-prime, nc-transcript-variant	SART1	GRCh38.p7	11:65979052	CCTCCCGCCCCGGCC[C/T]TGCCTCAACCTTCAT	9092
rs758882322	snp	C/T	3.33901e-05	0.00408582	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65966156	AAAAATGTGGAGCTG[C/T]GGAAGAAGAAGCCTG	9092
rs758936490	snp	C/T			intron-variant	SART1	GRCh38.p7	11:65970192	TGGGAGTTGCAGATA[C/T]CATGACACTGCATCC	9092
rs758958221	snp	C/T	0.000284616	0.0119259	missense, utr-variant-5-prime, nc-transcript-variant	SART1	GRCh38.p7	11:65962072	GTGAAGCGGGAGAAG[C/T]GCGATGACGGCTACG	9092
rs758983526	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65962624	TGTAGATTGTCTTGA[A/G]GATAGTAGGGAGCCA	9092
rs759027662	snp	A/G	1.6563e-05	0.00287771	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65977056	GACGAGGAACCGATC[A/G]TGAATAGGGGGCTGG	9092
rs759044062	snp	A/C	5.20729e-05	0.00510233	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65967694	AGGAAGGTGGAGCTC[A/C]ACCGCCGGGGTCCCC	9092
rs759055772	snp	C/T	1.8146e-05	0.00301209	intron-variant	SART1	GRCh38.p7	11:65977148	GGGCTTGGGTGCTGC[C/T]GCAGGTGCAGGCAGG	9092
rs759197059	snp	C/T	6.68539e-05	0.00578122	intron-variant	SART1	GRCh38.p7	11:65966222	GACCTGGCGCAGGCA[C/T]GGCCTGGGCAGGCTG	9092
rs759219784	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65971738	GCAGTTAAGGGTTTC[A/G]CAAAGGAGAGGTTCT	9092
rs759232447	in-del	-/AG	3.01264e-05	0.00388102	upstream-variant-2KB, frameshift-variant	SART1, TSGA10IP	GRCh38.p7	11:65959874	GAGGCCCCCAAGGAC[-/AG]AACCCACCGGCAGCC	9092
rs759256594	snp	C/T	2.17167e-05	0.00329513	intron-variant	SART1	GRCh38.p7	11:65967596	ATGAGGGTGAGGGCC[C/T]GGCCAGGGGGTGGGA	9092
rs759277070	snp	A/G	1.66804e-05	0.00288789	missense, utr-variant-5-prime, nc-transcript-variant	SART1	GRCh38.p7	11:65964091	GCCAGCTCCAAAACT[A/G]GCTCAGGCGATGCCT	9092
rs759390927	snp	C/T	1.70682e-05	0.00292127	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65965166	CAGCGAGAGGAGCTG[C/T]GGGAGAAGCTGGCGG	9092
rs759412975	snp	C/T	1.91631e-05	0.00309535	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65976739	CTGGAGCACGGTGAA[C/T]CTGGACGAGGAGAAG	9092
rs759458203	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65963599	CAATTCTCCTACCTC[A/G]GCCTCCCGAGTATCT	9092
rs759472638	in-del	-/G	1.65734e-05	0.00287862	intron-variant	SART1	GRCh38.p7	11:65965822	GACACTGGTGGCCTT[-/G]GCTACCGGAATCCCG	9092
rs759549111	snp	A/G	1.65151e-05	0.00287355	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65978837	GCCCCTGGGCACCGT[A/G]GCCCTGCTCCAGGAG	9092
rs759577062	snp	C/T			downstream-variant-500B	SART1	GRCh38.p7	11:65980234	GCACGGCTAGAGCTG[C/T]GGGGCTGAGTCTTAG	9092
rs759585151	snp	C/G	2.54126e-05	0.0035645	intron-variant	SART1	GRCh38.p7	11:65965297	CTTGAGTGGGGTGGG[C/G]AGCAGGAGCTGGGCT	9092
rs759638111	snp	C/T			intron-variant	SART1	GRCh38.p7	11:65964146	AGTGAGTACTGTCTC[C/T]CTTGTTTCTACTTTG	9092
rs759671961	snp	A/C			intron-variant	SART1	GRCh38.p7	11:65969550	GAACTCCTGGGCTCA[A/C]GGGATCCTCCTGCCT	9092
rs759709097	snp	A/G	4.3985e-05	0.00468941	intron-variant	SART1	GRCh38.p7	11:65977904	CACCCAAGGAGGTGA[A/G]CAGGGCCTTTTGCAG	9092
rs759715368	snp	C/T	4.36043e-05	0.00466908	intron-variant	SART1	GRCh38.p7	11:65965037	GGTGAGTGGCTCCCT[C/T]CTCTCCCCACCAGCC	9092
rs759774349	snp	A/C	1.84903e-05	0.00304053	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65976471	CCGAGCGGAAGGGGG[A/C]CATCGTGTTCAACGC	9092
rs759805665	snp	A/G	1.65255e-05	0.00287445	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	SART1	GRCh38.p7	11:65964551	GCTGAAACCCTTGGA[A/G]GTTAATGCCATCAAG	9092
rs759940858	snp	C/T	1.81338e-05	0.00301108	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65966473	GAGCTGGAGGAGATC[C/T]GGGCCAAGCTGCGGC	9092
rs759982807	snp	A/G	3.46987e-05	0.00416511	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65977846	GACGGCTACAAACCC[A/G]ACGTTAAGATCGAAT	9092
rs759992278	in-del	-/A			utr-variant-3-prime, downstream-variant-500B	SART1	GRCh38.p7	11:65979687	AATCCATAGAAAGAC[-/A]AAACGGCCACCTTGG	9092
rs760002035	snp	A/C/G	9.56251e-05	0.006914	intron-variant	SART1	GRCh38.p7	11:65978573	CACCCAGGGCCCTGC[A/C/G]TCTCCTCTCATGCCC	9092
rs760040633	snp	C/T	1.66161e-05	0.00288232	utr-variant-3-prime, nc-transcript-variant	SART1	GRCh38.p7	11:65979047	AGCGCCCTCCCGCCC[C/T]GGCCCTGCCTCAACC	9092
rs760071140	in-del	-/GGGTGTGGTG	1.67511e-05	0.00289401	intron-variant	SART1	GRCh38.p7	11:65978941	GAGGCTGGTGGGGTA[-/GGGTGTGGTG]GGGAGGGGTGGCGTG	9092
rs760136923	snp	G/T			intron-variant	SART1	GRCh38.p7	11:65975877	GCCCGTGTGGGGGTC[G/T]CTGGATTCAGTGCTG	9092
rs760141913	snp	C/G	0.000156419	0.00884222	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65966541	GGCCTCCGAATACCT[C/G]ACGCCTGAGGAGATG	9092
rs760168545	snp	C/T	1.66485e-05	0.00288513	intron-variant	SART1	GRCh38.p7	11:65978974	TGGCGTGGCCTGTGC[C/T]CGCCTCTGCAGCCTC	9092
rs760191311	snp	G/T	1.76783e-05	0.00297302	intron-variant	SART1	GRCh38.p7	11:65977140	ACTTGGGTGGGCTTG[G/T]GTGCTGCTGCAGGTG	9092
rs760300565	multinucleotide-polymorphism	ACG/GCA			intron-variant	SART1	GRCh38.p7	11:65973129	CAGTGAGCCGAGATC[ACG/GCA]CCACTGCACTCCAGC	9092
rs760308163	in-del	-/TG			intron-variant	SART1	GRCh38.p7	11:65966938	TGTCCACAGGGTGAC[-/TG]TGTGAACGTGAGGTA	9092
rs760357172	snp	C/G/T	2.58315e-05	0.00359375	synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	SART1	GRCh38.p7	11:65961846	GGCGGCGGCCGGCAC[C/G/T]GGGGGTGCCACCGAG	9092
rs760359561	snp	A/G	1.65946e-05	0.00288046	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65965750	GGTGTCAGCACTCTG[A/G]TGGAGGAGGAGTTCG	9092
rs760409069	snp	A/G	3.30945e-05	0.0040677	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65977045	CCACCATCCTGGACG[A/G]GGAACCGATCGTGAA	9092
rs760467496	in-del	-/G			intron-variant	SART1	GRCh38.p7	11:65968303	ATGCCTGCTTTAGTA[-/G]GGGATCCTTTCCTTG	9092
rs760544540	snp	G/T	2.11329e-05	0.00325054	intron-variant	SART1	GRCh38.p7	11:65967592	AGTGATGAGGGTGAG[G/T]GCCCGGCCAGGGGGT	9092
rs760696249	in-del	-/GCT			intron-variant	SART1	GRCh38.p7	11:65971606	TGGTGGGATTCAGGA[-/GCT]GCTGAGGAGGGGGAT	9092
rs760737553	snp	C/T	6.59739e-05	0.00574305	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65967343	GCAGATGACTTGCTG[C/T]CTCTCGGGGACCAGA	9092
rs760764642	snp	A/G	3.612e-05	0.00424955	intron-variant	SART1	GRCh38.p7	11:65964218	CTTTCTCACATGAAA[A/G]TGTGCTAATCAGAGT	9092
rs760803427	snp	C/T			downstream-variant-500B	SART1	GRCh38.p7	11:65980212	TGGCATTGATGCTGT[C/T]GCTTCTGCACGGCTA	9092
rs761094550	snp	C/T	1.8101e-05	0.00300835	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65977863	CGTTAAGATCGAATA[C/T]GTGGATGAGACGGGC	9092
rs761112002	snp	C/G	1.65247e-05	0.00287438	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	SART1	GRCh38.p7	11:65964539	GGCAAAGTTGGGGCT[C/G]AAACCCTTGGAGGTT	9092
rs761112338	snp	C/T	1.90159e-05	0.00308344	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65976457	GGAGGATGAGGATCC[C/T]GAGCGGAAGGGGGCC	9092
rs761194079	in-del	-/AA	1.68233e-05	0.00290023	frameshift-variant, nc-transcript-variant	SART1	GRCh38.p7	11:65966433	TTGGAGCAGGGCGGC[-/AA]ACGGCTGATGGCCTG	9092
rs761252156	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65973377	GTAGATAAGACAGGC[A/G]GTTCACAGAAGAGAA	9092
rs761305439	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65972283	GAGAGACCAGACAGC[A/G]GGGCCCCGAGACAGA	9092
rs761311893	snp	C/T	1.66482e-05	0.0028851	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65966405	TTGAAGGGGAGCGGC[C/T]ACATTCCTTCCGCTT	9092
rs761358159	snp	A/G	1.65154e-05	0.00287358	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65978895	ATCGTGCTCAGCGGC[A/G]GCGGCAAGAGCATGA	9092
rs761441104	in-del	-/CTC	9.54791e-05	0.00690872	intron-variant	SART1	GRCh38.p7	11:65978575	CCCAGGGCCCTGCAT[-/CTC]CTCTCATGCCCCGCG	9092
rs761488186	snp	A/G	2.01554e-05	0.00317448	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	SART1	GRCh38.p7	11:65961742	CATTTTGCGTTGTCT[A/G]GGCTCGGCGGCAGCC	9092
rs761499692	snp	C/G/T	6.84807e-05	0.00585118	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65966447	GCACGGCTGATGGCC[C/G/T]GCGGGAGCGGGAGCT	9092
rs761542453	snp	C/G			intron-variant	SART1	GRCh38.p7	11:65964865	GGGTTTCTTGTTTTT[C/G]TTTAAAGCACGATTT	9092
rs761664983	snp	C/T	4.96718e-05	0.00498331	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65977031	CTCTGCTTCCTCCAC[C/T]ACCATCCTGGACGAG	9092
rs761707434	snp	C/T			missense, nc-transcript-variant	SART1	GRCh38.p7	11:65966372	CTCGCTCTATCCTGT[C/T]CAAGTATGACGAAGA	9092
rs761747767	snp	A/G	1.67267e-05	0.0028919	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65966105	GAGGAGGACGTGCTG[A/G]TGAACGTGAACCTGG	9092
rs761754949	snp	C/G	5.6024e-05	0.00529234	intron-variant	SART1	GRCh38.p7	11:65976805	TGGGCGTTTGGGGGT[C/G]CTCAAGCTGGAGATG	9092
rs761756990	snp	C/T	1.65641e-05	0.00287781	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65979024	CAGGAACACCATCAC[C/T]AAGTGACAGCGCCCT	9092
rs761811706	snp	A/G	2.44813e-05	0.00349858	intron-variant	SART1	GRCh38.p7	11:65965291	CTGCCTCTTGAGTGG[A/G]GTGGGGAGCAGGAGC	9092
rs761829443	snp	A/C	1.69591e-05	0.00291191	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65967529	GAGAAGGAGCCTGTG[A/C]CTCAGCCCCTGCCGT	9092
rs761843410	in-del	-/CCT			intron-variant	SART1	GRCh38.p7	11:65976877	AGTGGGCTCTGCAGA[-/CCT]CCTCCCAGGGCGATC	9092
rs761853584	snp	A/G	1.71997e-05	0.0029325	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65976666	CCCAGGACTTTGAAC[A/G]GGATGAGGAGCGCTC	9092
rs761871110	snp	C/T	1.65466e-05	0.00287628	intron-variant	SART1	GRCh38.p7	11:65965848	TCCCGAGGTTGGGTG[C/T]GTGGAGGGAGGTTCC	9092
rs761933575	in-del	-/TGG			intron-variant	SART1	GRCh38.p7	11:65971134	TGCTGAGGAGGGGGA[-/TGG]TGGGATTCATGAGCT	9092
rs761935063	snp	A/C	1.72528e-05	0.00293703	intron-variant	SART1	GRCh38.p7	11:65976596	CGGCCCCGCCCTCTG[A/C]TTCCCTCGGCTGGGT	9092
rs761937096	snp	C/T	3.42718e-05	0.00413941	intron-variant	SART1	GRCh38.p7	11:65978733	CTGTGCCTGCCGGGG[C/T]AGGGGTGGCTGGTGT	9092
rs762003887	snp	A/G	3.16201e-05	0.00397606	upstream-variant-2KB, missense	SART1, TSGA10IP	GRCh38.p7	11:65959869	CCTCAGAGGCCCCCA[A/G]GGACAGAACCCACCG	9092
rs762025561	snp	A/G	3.29826e-05	0.00406082	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65967326	AGGAGGTAGTAGTGC[A/G]GGCAGATGACTTGCT	9092
rs762049645	snp	A/T	0.000334057	0.0129196	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65976731	AACATCGGCTGGAGC[A/T]CGGTGAACCTGGACG	9092
rs762165130	snp	C/G	2.08301e-05	0.00322717	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65967782	ACGCCGGCTGCGACA[C/G]TTACAGCAGCTACAG	9092
rs762211308	snp	A/T	1.65455e-05	0.00287619	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65977652	TGCATCGAGGATAAG[A/T]TGTGAGTGTGGTGGG	9092
rs762221647	snp	A/G	1.65168e-05	0.00287369	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65965914	GCCCGGGACCTGCAG[A/G]GCCTCACCGTGGAGC	9092
rs762255390	snp	C/T	6.61868e-05	0.00575231	intron-variant	SART1	GRCh38.p7	11:65977756	AGGCCTCCTCTGTCT[C/T]GGGCCAGGGCCATCG	9092
rs762417958	snp	A/G	3.48815e-05	0.00417607	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65967698	AGGTGGAGCTCCACC[A/G]CCGGGGTCCCCGCAG	9092
rs762449338	snp	A/G	1.66297e-05	0.0028835	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65966397	CGAAGAGCTTGAAGG[A/G]GAGCGGCCACATTCC	9092
rs762449691	snp	A/G	2.68756e-05	0.00366566	intron-variant	SART1	GRCh38.p7	11:65964195	CTCTGGGGCCAGCAC[A/G]GGGGAGGCTTTCTCA	9092
rs762507917	snp	C/G	1.65471e-05	0.00287633	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65977628	AAGTCGCTGCCCTCA[C/G]CCGTGTACTGCATCG	9092
rs762540261	snp	C/T	2.43288e-05	0.00348767	intron-variant	SART1	GRCh38.p7	11:65964189	AGGTGGCTCTGGGGC[C/T]AGCACGGGGGAGGCT	9092
rs762601469	snp	G/T	2.77327e-05	0.00372365	intron-variant	SART1	GRCh38.p7	11:65965310	GGGAGCAGGAGCTGG[G/T]CTCCTTGAGCATCAC	9092
rs762613445	snp	C/T	0.000112937	0.0075137	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65967770	GCTGGAGAAGGGACG[C/T]CGGCTGCGACAGTTA	9092
rs762626496	snp	A/G	7.89609e-05	0.00628285	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65976746	ACGGTGAACCTGGAC[A/G]AGGAGAAGCAGCAGC	9092
rs762646951	snp	C/T	0.000190114	0.00974787	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65965376	GAGGATGACCCCTGG[C/T]TGGACGACACTGCAG	9092
rs762712058	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65963863	TCTTGGGTCAGGAAA[A/G]GAAGGTGCACAGAAG	9092
rs762725337	in-del	-/G	3.35683e-05	0.00409671	intron-variant	SART1	GRCh38.p7	11:65966244	GGCAGGCTGGGTGGC[-/G]GGGGCTGAGGTGGAG	9092
rs762816180	in-del	-/C	1.65567e-05	0.00287716	intron-variant	SART1	GRCh38.p7	11:65977688	TGCAGGGCTGAGGGG[-/C]CTGTGCCAGCTTGGA	9092
rs762818213	snp	A/G	1.66829e-05	0.00288811	intron-variant	SART1	GRCh38.p7	11:65978947	GGTGGGGTAGGGTGT[A/G]GTGGGGAGGGGTGGC	9092
rs762892153	snp	A/G	6.64982e-05	0.00576582	intron-variant	SART1	GRCh38.p7	11:65967452	ACCGGTGCTCACCAG[A/G]GAGGCCTCCTTCCCT	9092
rs762901541	snp	C/G	1.65157e-05	0.0028736	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65978888	CCCCTACATCGTGCT[C/G]AGCGGCAGCGGCAAG	9092
rs762978400	snp	G/T	4.26212e-05	0.00461614	intron-variant	SART1	GRCh38.p7	11:65976798	TGGGGGGTGGGCGTT[G/T]GGGGGTGCTCAAGCT	9092
rs763010445	snp	C/T	2.03593e-05	0.00319049	intron-variant, utr-variant-5-prime	SART1	GRCh38.p7	11:65965051	TCCTCTCCCCACCAG[C/T]CATGGGCGGGCATAG	9092
rs763025743	snp	C/T	1.69772e-05	0.00291347	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	SART1	GRCh38.p7	11:65961734	AGTATTCCCATTTTG[C/T]GTTGTCTGGGCTCGG	9092
rs763114176	snp	C/T	3.44222e-05	0.00414848	intron-variant	SART1	GRCh38.p7	11:65976587	CGTCTGGGGCGGCCC[C/T]GCCCTCTGCTTCCCT	9092
rs763145998	snp	C/T			intron-variant	SART1	GRCh38.p7	11:65976136	GGAGGGGGATTGGCA[C/T]AGGCCTGGTCAGGAA	9092
rs763157832	snp	C/G	3.37427e-05	0.00410734	intron-variant	SART1	GRCh38.p7	11:65977916	TGAGCAGGGCCTTTT[C/G]CAGGCGGAGGCCCGG	9092
rs763174089	snp	G/T	1.72145e-05	0.00293376	intron-variant	SART1	GRCh38.p7	11:65976649	ACCCTGGTCTTTTGT[G/T]CCCCAGGACTTTGAA	9092
rs763200833	snp	C/T	1.64789e-05	0.0028704	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	SART1	GRCh38.p7	11:65965126	GCCCGTGACAGCTGA[C/T]GTCATCAACCCTATG	9092
rs763211856	snp	C/T	6.56642e-05	0.00572955	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65966545	TCCGAATACCTCACG[C/T]CTGAGGAGATGGTGA	9092
rs763329378	snp	A/C	4.99946e-05	0.00499948	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	SART1	GRCh38.p7	11:65964105	TAGCTCAGGCGATGC[A/C]TCCTCACTCAGCATC	9092
rs763406087	snp	A/C	1.65946e-05	0.00288046	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65965769	AGGAGGAGTTCGGGC[A/C]GAGGCGGCAGGTGAG	9092
rs763423258	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65967185	GAACACCAAAGAAGT[A/G]TTCACCCTCGAGGGC	9092
rs763425130	in-del	-/C			intron-variant	SART1	GRCh38.p7	11:65977413	AGGGGCTCATTTCTG[-/C]CATCTTTGCTTTGCC	9092
rs763505096	snp	C/T			downstream-variant-500B	SART1	GRCh38.p7	11:65980303	GTGCAGCGGGAGCTG[C/T]GGGGCTGAGTCTTTG	9092
rs763607912	snp	A/C	1.65671e-05	0.00287807	intron-variant	SART1	GRCh38.p7	11:65965831	TGGCCTTGCTACCGG[A/C]ATCCCGAGGTTGGGT	9092
rs763641883	snp	A/G/T	4.3767e-05	0.00467781	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65967701	TGGAGCTCCACCGCC[A/G/T]GGGTCCCCGCAGGTG	9092
rs763642434	snp	C/T	6.65945e-05	0.00576999	intron-variant	SART1	GRCh38.p7	11:65978762	GTGTGGGGCCTGCTG[C/T]AGCCCTTTCTGAGTG	9092
rs763667540	snp	A/C	2.81734e-05	0.00375312	intron-variant	SART1	GRCh38.p7	11:65965314	GCAGGAGCTGGGCTC[A/C]TTGAGCATCACTTTT	9092
rs763701830	in-del	-/GGGCTCGGCGGCAGCC	6.04309e-05	0.00549652	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	SART1	GRCh38.p7	11:65961741	CATTTTGCGTTGTCT[-/GGGCTCGGCGGCAGCC]GGGCTCGGCGGCAGC	9092
rs763711048	snp	C/G	3.3583e-05	0.0040976	intron-variant	SART1	GRCh38.p7	11:65966259	GGGGGCTGAGGTGGA[C/G]AATGTCGGGAATGGG	9092
rs763789662	in-del	-/CT			utr-variant-3-prime	SART1	GRCh38.p7	11:65980104	GGTGACAGTCAGACC[-/CT]GTCTCAAAAAAAATA	9092
rs763789733	in-del	-/G	1.68291e-05	0.00290073	intron-variant	SART1	GRCh38.p7	11:65966266	GAGGTGGAGAATGTC[-/G]GGAATGGGGGCTCTG	9092
rs763883673	snp	C/T	1.65018e-05	0.00287239	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65967366	GGACCAGACTCAGGA[C/T]GGGGACTTTGGTTCC	9092
rs763959848	snp	A/T	6.04041e-05	0.00549531	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	SART1	GRCh38.p7	11:65961737	ATTCCCATTTTGCGT[A/T]GTCTGGGCTCGGCGG	9092
rs764007861	snp	A/G	3.30967e-05	0.00406783	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65965956	TCCTTCCGAGAAGGG[A/G]AGACAATGATTCTTA	9092
rs764047910	snp	C/T	5.73268e-05	0.00535352	upstream-variant-2KB, synonymous-codon	SART1, TSGA10IP	GRCh38.p7	11:65959917	CACTACAACCCCAGC[C/T]TGGACCCGGAGTGCA	9092
rs764124258	snp	A/G			missense, nc-transcript-variant	SART1	GRCh38.p7	11:65966476	CTGGAGGAGATCCGG[A/G]CCAAGCTGCGGCTGC	9092
rs764143934	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65964727	TTGCTGGTATAATGG[A/G]GATCTGGGGCTCCGC	9092
rs764144013	snp	C/G			intron-variant	SART1	GRCh38.p7	11:65970421	ACCGGAGATTCTAGA[C/G]TATGTGGGAGACACA	9092
rs764148984	snp	A/T	2.02288e-05	0.00318025	intron-variant, utr-variant-5-prime	SART1	GRCh38.p7	11:65965053	CTCTCCCCACCAGCC[A/T]TGGGCGGGCATAGCC	9092
rs764231239	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65976918	ATGAGGAAATTAAAT[A/G]TTGTGGAGGGCTGGT	9092
rs764257650	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65978783	TTTCTGAGTGGCCCC[A/G]ACCCCTCAGCTCCTG	9092
rs764352821	snp	C/T	1.66593e-05	0.00288607	utr-variant-3-prime, nc-transcript-variant	SART1	GRCh38.p7	11:65979058	GCCCCGGCCCTGCCT[C/T]AACCTTCATATTAAA	9092
rs764366932	snp	C/T	9.96529e-05	0.00705808	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65966546	CCGAATACCTCACGC[C/T]TGAGGAGATGGTGAG	9092
rs764457642	in-del	-/AT			intron-variant	SART1	GRCh38.p7	11:65967132	CCCCACATGTTGCTC[-/AT]GTGTGGGAAGCGCTC	9092
rs764507558	snp	C/T	3.31016e-05	0.00406813	intron-variant	SART1	GRCh38.p7	11:65965836	TTGCTACCGGAATCC[C/T]GAGGTTGGGTGCGTG	9092
rs764597455	snp	C/T	1.65996e-05	0.00288089	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65965774	GAGTTCGGGCAGAGG[C/T]GGCAGGTGAGGCTGC	9092
rs764613050	snp	A/G	4.38423e-05	0.0046818	intron-variant	SART1	GRCh38.p7	11:65967597	TGAGGGTGAGGGCCC[A/G]GCCAGGGGGTGGGAG	9092
rs764703889	snp	C/T	1.66732e-05	0.00288727	missense, utr-variant-5-prime, nc-transcript-variant	SART1	GRCh38.p7	11:65964107	GCTCAGGCGATGCCT[C/T]CTCACTCAGCATCGA	9092
rs764753643	snp	C/T			intron-variant	SART1	GRCh38.p7	11:65973505	TTCCGCAGAAAGGTC[C/T]AAGCCTGACAGTAGC	9092
rs764778388	snp	A/G	1.85379e-05	0.00304444	intron-variant	SART1	GRCh38.p7	11:65977153	TGGGTGCTGCTGCAG[A/G]TGCAGGCAGGGCCCC	9092
rs764810513	snp	C/T	1.67508e-05	0.00289398	intron-variant	SART1	GRCh38.p7	11:65966236	ACGGCCTGGGCAGGC[C/T]GGGTGGCGGGGGCTG	9092
rs764853353	in-del	-/CT			intron-variant	SART1	GRCh38.p7	11:65971766	TCTGTTGATTTCCCC[-/CT]GAGTCTAAACTGGGT	9092
rs764861341	snp	A/C			utr-variant-3-prime, downstream-variant-500B	SART1	GRCh38.p7	11:65979562	GGGAGGGCTGAGCTC[A/C]GTGCCTCCTGGGAGA	9092
rs764875856	snp	C/T	1.65105e-05	0.00287315	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65978873	GAAGGCTCAGAAGAC[C/T]CCCTACATCGTGCTC	9092
rs764885292	snp	C/T			intron-variant	SART1	GRCh38.p7	11:65962640	GATAGTAGGGAGCCA[C/T]GGATGTGAGTTGAGG	9092
rs765024561	in-del	-/CCGGAG	5.63544e-05	0.00530792	upstream-variant-2KB, cds-indel	SART1, TSGA10IP	GRCh38.p7	11:65959923	AACCCCAGCCTGGAC[-/CCGGAG]TGCAGTCCCTGAGAT	9092
rs765077904	snp	G/T	2.59858e-05	0.00360448	intron-variant	SART1	GRCh38.p7	11:65965299	TGAGTGGGGTGGGGA[G/T]CAGGAGCTGGGCTCC	9092
rs765100178	snp	C/T	1.81688e-05	0.00301398	upstream-variant-2KB, intron-variant	SART1, TSGA10IP	GRCh38.p7	11:65959801	AGAGTCAGGGGCCTC[C/T]ATCTGTGTCTTGAAG	9092
rs765122173	snp	G/T	1.66241e-05	0.00288302	intron-variant	SART1	GRCh38.p7	11:65966341	CAACCTGTACCTCTT[G/T]CCTTGCAGCAAAAAC	9092
rs765161734	snp	C/T			intron-variant	SART1	GRCh38.p7	11:65969574	CCTGCCTCAGGCTCT[C/T]AAGTAGCTGAGACTA	9092
rs765223260	snp	C/G			intron-variant	SART1	GRCh38.p7	11:65962283	GCAGTGAGCTGCGGT[C/G]CCGCCAGTGTACTCC	9092
rs765256197	snp	A/G	3.30524e-05	0.00406511	missense, utr-variant-5-prime, nc-transcript-variant	SART1	GRCh38.p7	11:65964561	TTGGAGGTTAATGCC[A/G]TCAAGAAGGGTGAGT	9092
rs765256753	snp	A/G	1.65723e-05	0.00287852	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65977787	ATGACAAGTACAGCC[A/G]GAGGGAGGAATACCG	9092
rs765273976	snp	A/C	2.3548e-05	0.00343124	upstream-variant-2KB, missense	SART1, TSGA10IP	GRCh38.p7	11:65959889	AGAACCCACCGGCAG[A/C]CAGCCTGACAGGCAC	9092
rs765296181	snp	A/G	1.65181e-05	0.00287381	intron-variant	SART1	GRCh38.p7	11:65977906	CCCAAGGAGGTGAGC[A/G]GGGCCTTTTGCAGGC	9092
rs765341930	snp	A/C/G/T	0.000117276	0.00765682	intron-variant	SART1	GRCh38.p7	11:65966037	CCTCTGCTGAGTTGC[A/C/G/T]GACAAGTGTGAATGG	9092
rs765454444	snp	A/C	4.19762e-05	0.00458109	intron-variant	SART1	GRCh38.p7	11:65965046	CTCCCTCCTCTCCCC[A/C]CCAGCCATGGGCGGG	9092
rs765480531	snp	C/G/T	3.38806e-05	0.00411575	intron-variant	SART1	GRCh38.p7	11:65965690	CCTAGGTCACCCCTC[C/G/T]CTGTCCCGTAGGCCA	9092
rs765544283	snp	C/T	5.51821e-05	0.00525243	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65976475	GCGGAAGGGGGCCAT[C/T]GTGTTCAACGCCACG	9092
rs765643779	in-del	-/AGCTGAGGAGGGGGATGGTGGGATTCATG			intron-variant	SART1	GRCh38.p7	11:65971177	ATGGTGGGATTCAGA[lengthTooLong]AGCTGAGGAGGGGGA	9092
rs765657973	snp	A/G	3.19249e-05	0.00399518	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65966542	GCCTCCGAATACCTC[A/G]CGCCTGAGGAGATGG	9092
rs765679321	snp	C/G	3.92935e-05	0.00443229	synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	SART1	GRCh38.p7	11:65961879	GCCGCCGCGGCACCG[C/G]GAACACAAAAAACAC	9092
rs765687940	in-del	-/C	1.68155e-05	0.00289956	utr-variant-3-prime, nc-transcript-variant	SART1	GRCh38.p7	11:65979081	ATATTAAATAAAGCT[-/C]CCTCCTTATTTTTTC	9092
rs765745984	snp	A/G	5.48561e-05	0.00523689	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65966474	AGCTGGAGGAGATCC[A/G]GGCCAAGCTGCGGCT	9092
rs765789161	snp	C/G	1.65902e-05	0.00288008	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65965761	TCTGGTGGAGGAGGA[C/G]TTCGGGCAGAGGCGG	9092
rs765939069	snp	A/G	1.70869e-05	0.00292286	intron-variant	SART1	GRCh38.p7	11:65976981	AGAAGAGCCGGTATG[A/G]CCTGCTAACCACCCC	9092
rs765955298	snp	A/C			upstream-variant-2KB	SART1	GRCh38.p7	11:65961589	CCACCCGACCCGAGA[A/C]GGCGCGAATGTGCAG	9092
rs765960925	snp	A/C			upstream-variant-2KB, downstream-variant-500B, utr-variant-3-prime	SART1, TSGA10IP	GRCh38.p7	11:65960289	GGGGGTGGATCCTTA[A/C]AGGGGCGCATACAAC	9092
rs766048167	snp	C/T	0.000232261	0.0107739	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	SART1	GRCh38.p7	11:65962047	CCAGGCAGAGCCCTC[C/T]GAGCGGCGCGTGAAG	9092
rs766076045	snp	A/G			utr-variant-3-prime, downstream-variant-500B	SART1	GRCh38.p7	11:65979374	GGTCACTGTCCTGTA[A/G]TGTCTCCCGGTCAGG	9092
rs766126860	snp	A/C/G	3.34422e-05	0.00408903	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65967476	CTTCCCTCAGACTGC[A/C/G]GGGACGGGGTCGCCG	9092
rs766145739	snp	C/T	5.83448e-05	0.00540083	intron-variant, utr-variant-5-prime	SART1	GRCh38.p7	11:65965067	CATGGGCGGGCATAG[C/T]CTCACGTCTGGGCCC	9092
rs766231339	snp	A/G	1.7122e-05	0.00292587	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65965149	ACCCTATGGCCTTGC[A/G]ACAGCGAGAGGAGCT	9092
rs766296058	snp	C/G	3.44697e-05	0.00415134	intron-variant	SART1	GRCh38.p7	11:65976599	CCCCGCCCTCTGCTT[C/G]CCTCGGCTGGGTGGG	9092
rs766302263	snp	A/G	1.70769e-05	0.00292202	intron-variant	SART1	GRCh38.p7	11:65978735	GTGCCTGCCGGGGCA[A/G]GGGTGGCTGGTGTGT	9092
rs766319644	snp	G/T	6.35519e-05	0.00563666	intron-variant	SART1	GRCh38.p7	11:65967593	GTGATGAGGGTGAGG[G/T]CCCGGCCAGGGGGTG	9092
rs766344694	snp	C/T			utr-variant-3-prime, downstream-variant-500B	SART1	GRCh38.p7	11:65979489	TGCCACCCTGGTCTG[C/T]GTCTAGAGGAGTGAA	9092
rs766394491	snp	A/G	4.95733e-05	0.00497837	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65965928	GGGCCTCACCGTGGA[A/G]CATGCCATTGATTCC	9092
rs766484641	snp	A/G	1.64942e-05	0.00287173	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65967352	TTGCTGCCTCTCGGG[A/G]ACCAGACTCAGGATG	9092
rs766511006	snp	A/G/T	3.31166e-05	0.00406908	intron-variant	SART1	GRCh38.p7	11:65977672	AGTGTGGTGGGGCCT[A/G/T]TGCAGGGCTGAGGGG	9092
rs766573779	snp	C/T			intron-variant	SART1	GRCh38.p7	11:65968458	GTGTGTGGGGGAGAG[C/T]GTGGGGAGCAGCAGT	9092
rs766591106	snp	C/T	1.67022e-05	0.00288978	intron-variant	SART1	GRCh38.p7	11:65966024	GGTGGGGGCACAGCC[C/T]CTGCTGAGTTGCGGA	9092
rs766609883	snp	C/T	0.000150184	0.00866426	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65966416	CGGCCACATTCCTTC[C/T]GCTTGGAGCAGGGCG	9092
rs766617195	snp	C/G			intron-variant	SART1	GRCh38.p7	11:65973792	GTGGAAACTGATGAG[C/G]TACAGCCGTGTGCAT	9092
rs766624818	snp	C/T	3.98034e-05	0.00446095	intron-variant	SART1	GRCh38.p7	11:65964223	TCACATGAAAGTGTG[C/T]TAATCAGAGTTGGAA	9092
rs766699778	in-del	-/GTAA			intron-variant	SART1	GRCh38.p7	11:65969251	CAGCCAAGACAGTCT[-/GTAA]GTGAGTGGGCGTGGC	9092
rs766707178	snp	A/G	1.6557e-05	0.00287719	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65977779	GGCCATCGATGACAA[A/G]TACAGCCGGAGGGAG	9092
rs766709991	snp	A/G	3.30497e-05	0.00406494	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	SART1	GRCh38.p7	11:65964548	GGGGCTGAAACCCTT[A/G]GAGGTTAATGCCATC	9092
rs766848879	in-del	-/GATT			intron-variant	SART1	GRCh38.p7	11:65972412	CACACCTTGCAGATA[-/GATT]AAGAACTTCAAAGTA	9092
rs766881196	snp	A/G	1.6736e-05	0.0028927	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65965400	ACTGCAGCCTGGATC[A/G]AGAGGAGCCGGCAGC	9092
rs766916524	snp	G/T			intron-variant	SART1	GRCh38.p7	11:65964928	GTGCTGCATGGGTTG[G/T]CCAGGAGTGTGGGGA	9092
rs766921064	snp	C/G	1.74955e-05	0.00295761	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65966461	CTGCGGGAGCGGGAG[C/G]TGGAGGAGATCCGGG	9092
rs766925965	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65969885	ATGCCACCACGCCCA[A/G]CTGATTTTTGTATTT	9092
rs766952326	in-del	-/G	3.76903e-05	0.00434094	intron-variant	SART1	GRCh38.p7	11:65978709	TGCCCTTGGGGATGT[-/G]GGGGGGCCCTGTGCC	9092
rs766955213	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65975951	CTTGGTGAAGCAGGA[A/G]GCGAGAAGCTGGGCT	9092
rs766962974	snp	G/T	5.32382e-05	0.0051591	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65965391	CTGGACGACACTGCA[G/T]CCTGGATCGAGAGGA	9092
rs766974192	in-del	-/C	1.68955e-05	0.00290645	intron-variant	SART1	GRCh38.p7	11:65967224	CCTGCCTTTCTGTGG[-/C]CCCCCGCTCCATGTC	9092
rs767006601	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65973494	CCTGCCAACAATTCC[A/G]CAGAAAGGTCCAAGC	9092
rs767006661	snp	C/T	0.0002429	0.0110177	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65976697	AGCCAACGGTGGCTC[C/T]GAATCTGACGGGGAG	9092
rs767077769	snp	A/G	1.65466e-05	0.00287628	intron-variant	SART1	GRCh38.p7	11:65976778	GGATGTGAGGGCCGC[A/G]CCGCTGGGGGGTGGG	9092
rs767079262	snp	A/G	2.01436e-05	0.00317355	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	SART1	GRCh38.p7	11:65961744	TTTTGCGTTGTCTGG[A/G]CTCGGCGGCAGCCGG	9092
rs767157332	snp	A/G	6.84709e-05	0.0058507	intron-variant	SART1	GRCh38.p7	11:65965678	GTGGCCTGAAGTCCT[A/G]GGTCACCCCTCCCTG	9092
rs767307580	snp	C/T	1.67435e-05	0.00289335	intron-variant	SART1	GRCh38.p7	11:65966044	TGAGTTGCGGACAAG[C/T]GTGAATGGCCACTGC	9092
rs767376560	snp	C/T	1.70145e-05	0.00291667	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65967538	CCTGTGCCTCAGCCC[C/T]TGCCGTCGGACGACA	9092
rs767403436	snp	A/G	9.59762e-05	0.00692668	synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	SART1	GRCh38.p7	11:65961831	GGCGGCCGGGACGAC[A/G]GCGGCGGCCGGCACC	9092
rs767472442	snp	C/T	3.33439e-05	0.00408299	intron-variant	SART1	GRCh38.p7	11:65967465	AGAGAGGCCTCCTTC[C/T]CTCAGACTGCGGGGA	9092
rs767547085	snp	C/T	4.68834e-05	0.00484144	intron-variant	SART1	GRCh38.p7	11:65966562	TGAGGAGATGGTGAG[C/T]CCTCCCGTGCCTTAT	9092
rs767599562	snp	C/T	5.33149e-05	0.00516281	upstream-variant-2KB, missense	SART1, TSGA10IP	GRCh38.p7	11:65959882	CAAGGACAGAACCCA[C/T]CGGCAGCCAGCCTGA	9092
rs767637447	snp	C/G	1.71784e-05	0.00293069	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65976668	CAGGACTTTGAACGG[C/G]ATGAGGAGCGCTCAG	9092
rs767682662	snp	C/T			intron-variant	SART1	GRCh38.p7	11:65966700	GCACTAAATGGCAAC[C/T]GGGGGAGGCACCAGG	9092
rs767704398	snp	A/G	7.71575e-05	0.0062107	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65967704	AGCTCCACCGCCGGG[A/G]TCCCCGCAGGTGCTG	9092
rs767737554	snp	A/G			missense, nc-transcript-variant	SART1	GRCh38.p7	11:65967334	GTAGTGCGGGCAGAT[A/G]ACTTGCTGCCTCTCG	9092
rs767740911	snp	A/C			utr-variant-3-prime, downstream-variant-500B	SART1	GRCh38.p7	11:65979297	CCGGCTCTCTGATAG[A/C]AAGTGGAAGGCGGTT	9092
rs767792464	snp	G/T	8.27274e-05	0.00643093	intron-variant	SART1	GRCh38.p7	11:65977660	GGATAAGATGTGAGT[G/T]TGGTGGGGCCTGTGC	9092
rs767815063	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65975706	AAATGAAAGAGGGGT[A/G]CAGAAGTGGACATAG	9092
rs767833616	snp	G/T	1.65162e-05	0.00287365	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65965915	CCCGGGACCTGCAGG[G/T]CCTCACCGTGGAGCA	9092
rs767961850	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65962876	CTTGTATGAGGGTGG[A/G]AAGAAGGAATGGAGG	9092
rs767971646	snp	C/G	5.4444e-05	0.00521719	intron-variant	SART1	GRCh38.p7	11:65964196	TCTGGGGCCAGCACG[C/G]GGGAGGCTTTCTCAC	9092
rs768097360	snp	C/G	1.65441e-05	0.00287607	intron-variant	SART1	GRCh38.p7	11:65977744	CTCCTCACACTAAGG[C/G]CTCCTCTGTCTCGGG	9092
rs768170253	snp	C/T	3.46566e-05	0.00416259	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65977845	GGACGGCTACAAACC[C/T]GACGTTAAGATCGAA	9092
rs768317954	snp	C/T	0.000120751	0.00776923	intron-variant	SART1	GRCh38.p7	11:65965657	AGTGTTTTCTGGTGA[C/T]GCTGAGTGGCCTGAA	9092
rs768337449	snp	A/G	1.66463e-05	0.00288494	intron-variant	SART1	GRCh38.p7	11:65965999	AAGGTAATGCGAGCT[A/G]GGTGCCCTGGGTGGG	9092
rs768391119	in-del	-/C	1.65488e-05	0.00287647	intron-variant	SART1	GRCh38.p7	11:65977705	TGTGCCAGCTTGGAG[-/C]TTCGGGACCACAGCA	9092
rs768429434	snp	C/T			intron-variant	SART1	GRCh38.p7	11:65977428	GCATCTTTGCTTTGC[C/T]TGTAGAACAGGCCTG	9092
rs768482793	snp	C/T			intron-variant	SART1	GRCh38.p7	11:65975396	ATGTGAGCAACCACC[C/T]GGCCCCTGGAAGAAT	9092
rs768494886	snp	C/T	1.65578e-05	0.00287726	intron-variant	SART1	GRCh38.p7	11:65979009	CCCTGTTCTTCTCTG[C/T]AGGAACACCATCACC	9092
rs768508713	snp	G/T	2.07097e-05	0.00321783	missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	SART1	GRCh38.p7	11:65961813	GCATCGCGGAGAGAA[G/T]GAGGCGGCCGGGACG	9092
rs768579159	snp	C/T	6.52997e-05	0.00571363	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	SART1	GRCh38.p7	11:65961963	CCGGGAACGTGGGGG[C/T]GAGCGCGGGAGCGGG	9092
rs768592762	snp	A/G	4.99596e-05	0.00499773	intron-variant	SART1	GRCh38.p7	11:65978952	GGTAGGGTGTGGTGG[A/G]GAGGGGTGGCGTGGC	9092
rs768594116	snp	C/G	1.66718e-05	0.00288715	intron-variant	SART1	GRCh38.p7	11:65966317	CTTTTCAGGAGCCAG[C/G]CTGGGTCCCAACCTG	9092
rs768624224	snp	A/G	0.00016645	0.00912126	intron-variant	SART1	GRCh38.p7	11:65977010	CCCGCCACGTGTCCC[A/G]TAGTTCTCTGCTTCC	9092
rs768641788	snp	C/G			intron-variant	SART1	GRCh38.p7	11:65972482	CATTTATAACTTTTT[C/G]GTAGAAAAGATTTTT	9092
rs768743338	snp	A/C	1.72175e-05	0.00293402	intron-variant	SART1	GRCh38.p7	11:65976650	CCCTGGTCTTTTGTG[A/C]CCCAGGACTTTGAAC	9092
rs768756881	snp	A/G	1.71911e-05	0.00293177	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65965139	GATGTCATCAACCCT[A/G]TGGCCTTGCGACAGC	9092
rs768761142	snp	C/T			intron-variant	SART1	GRCh38.p7	11:65967898	GTCATAGGCGACAGC[C/T]ACATTCCTGTCTGAA	9092
rs768788233	snp	G/T	3.58429e-05	0.00423322	intron-variant	SART1	GRCh38.p7	11:65965251	GGGCAGGCAAGGGAA[G/T]GGCTGGGGAGGCCAC	9092
rs768807897	snp	G/T	1.6607e-05	0.00288153	upstream-variant-2KB, missense	SART1, TSGA10IP	GRCh38.p7	11:65959859	GGAGCACTCTCCTCA[G/T]AGGCCCCCAAGGACA	9092
rs768811870	in-del	-/ATT			intron-variant	SART1	GRCh38.p7	11:65975811	GGGGAGATGGTAATC[-/ATT]GTGTGTGGCTGGGCA	9092
rs768843222	snp	C/G	1.6671e-05	0.00288708	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65966197	CTATGCCGAGGACGA[C/G]AGCGTGGACGACCTG	9092
rs768865341	snp	C/T	3.75862e-05	0.00433494	intron-variant	SART1	GRCh38.p7	11:65965332	GAGCATCACTTTTTC[C/T]CCTCTTCAGGAAGAT	9092
rs768927618	snp	C/T	4.62396e-05	0.00480808	intron-variant	SART1	GRCh38.p7	11:65967664	CTGAGCAGGCATCCC[C/T]TGTGTTTCCCCCAGA	9092
rs768999990	snp	A/G	3.54164e-05	0.00420796	upstream-variant-2KB, utr-variant-3-prime	SART1, TSGA10IP	GRCh38.p7	11:65959950	CCCTGAGATAAAATT[A/G]AAGGCTTTATGGCAA	9092
rs769020745	snp	A/G	1.64939e-05	0.0028717	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65967315	CAAGAAGGAGAAGGA[A/G]GTAGTAGTGCGGGCA	9092
rs769028019	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65962337	CTGTCTCAAAAAGAA[A/G]AAAGTCTTTCTACGG	9092
rs769087695	snp	A/G			upstream-variant-2KB	SART1	GRCh38.p7	11:65961526	CTCCGGGTTAATTCC[A/G]CTTCCCTTGAGGAGC	9092
rs769102326	snp	A/G	3.50275e-05	0.0041848	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65976707	GGCTCCGAATCTGAC[A/G]GGGAGGAGAACATCG	9092
rs769161903	snp	C/T			intron-variant	SART1	GRCh38.p7	11:65967204	ACCCTCGAGGGCTTG[C/T]GGCGACCTGCCTTTC	9092
rs769226520	snp	C/T	4.96504e-05	0.00498224	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65977617	AGGCCCCCAACAAGT[C/T]GCTGCCCTCAGCCGT	9092
rs769274713	snp	A/G	1.6557e-05	0.00287719	intron-variant	SART1	GRCh38.p7	11:65964475	CACATGGCACCCTGT[A/G]TCTTTAATAGCCCCT	9092
rs769293764	snp	A/G	1.65173e-05	0.00287374	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65965912	GTGCCCGGGACCTGC[A/G]GGGCCTCACCGTGGA	9092
rs769419224	snp	C/T	1.65699e-05	0.00287831	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65977786	GATGACAAGTACAGC[C/T]GGAGGGAGGAATACC	9092
rs769428234	snp	C/G/T	3.32371e-05	0.00407647	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65966389	AAGTATGACGAAGAG[C/G/T]TTGAAGGGGAGCGGC	9092
rs769474414	snp	A/G	3.48062e-05	0.00417156	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65967695	GGAAGGTGGAGCTCC[A/G]CCGCCGGGGTCCCCG	9092
rs769498116	snp	A/G	6.60044e-05	0.00574438	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65967299	GGGTGAAGAAAATCC[A/G]CAAGAAGGAGAAGGA	9092
rs769710645	snp	A/G	1.81118e-05	0.00300925	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65967572	GAGTGGAGAACATGG[A/G]CATCAGTGATGAGGG	9092
rs769759565	snp	G/T	0.0001033	0.00718607	intron-variant	SART1	GRCh38.p7	11:65978939	TCGAGGCTGGTGGGG[G/T]AGGGTGTGGTGGGGA	9092
rs769814338	in-del	-/CAA	3.31022e-05	0.00406817	cds-indel, nc-transcript-variant	SART1	GRCh38.p7	11:65977609	CCGGGTGAAGGCCCC[-/CAA]CAAGTCGCTGCCCTC	9092
rs769859433	snp	A/G	8.65127e-05	0.00657639	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65965363	AAAGACCCTAGGAGA[A/G]GATGACCCCTGGCTG	9092
rs769899656	in-del	-/T			intron-variant	SART1	GRCh38.p7	11:65976911	GAGTAAATGAGGAAA[-/T]TTAAATGTTGTGGAG	9092
rs769954106	snp	C/G	1.69149e-05	0.00290812	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65967522	GGAGGAGGAGAAGGA[C/G]CCTGTGCCTCAGCCC	9092
rs769969599	snp	A/G			missense, utr-variant-5-prime, nc-transcript-variant	SART1	GRCh38.p7	11:65964556	AACCCTTGGAGGTTA[A/G]TGCCATCAAGAAGGG	9092
rs769978369	snp	A/G			upstream-variant-2KB, downstream-variant-500B	SART1, TSGA10IP	GRCh38.p7	11:65960828	CAGGGATACACTGAC[A/G]CCCATGTGGAGCTCC	9092
rs770029259	snp	C/G	3.39466e-05	0.00411973	intron-variant	SART1	GRCh38.p7	11:65977110	AACAAAGGTAGGGAG[C/G]TCAGGGCAGCCATGA	9092
rs770116159	snp	A/G	1.76424e-05	0.00297	intron-variant	SART1	GRCh38.p7	11:65965236	GAGGGGTCCTGGCCA[A/G]GGCAGGCAAGGGAAG	9092
rs770125193	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65967172	GGCTAGCACAGAGGA[A/G]CACCAAAGAAGTGTT	9092
rs770212951	snp	A/G			missense, nc-transcript-variant	SART1	GRCh38.p7	11:65978637	GCTTCCATGGCAAGG[A/G]CTCAGGCAAGATGAA	9092
rs770242121	snp	G/T	1.86339e-05	0.00305231	intron-variant	SART1	GRCh38.p7	11:65978711	GCCCTTGGGGATGTG[G/T]GGGGCCCTGTGCCTG	9092
rs770293260	snp	A/G			missense, nc-transcript-variant	SART1	GRCh38.p7	11:65977858	CCCGACGTTAAGATC[A/G]AATACGTGGATGAGA	9092
rs770308687	snp	G/T	1.68108e-05	0.00289916	upstream-variant-2KB, missense	SART1, TSGA10IP	GRCh38.p7	11:65959833	AGCCACAGGTCAATG[G/T]GGGTGAGAATGGAGC	9092
rs770323333	snp	A/G	1.65932e-05	0.00288034	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65965752	TGTCAGCACTCTGGT[A/G]GAGGAGGAGTTCGGG	9092
rs770413448	snp	A/G	2.99451e-05	0.00386932	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65966537	GGCTGGCCTCCGAAT[A/G]CCTCACGCCTGAGGA	9092
rs770426207	snp	C/T	0.000198275	0.00995481	intron-variant	SART1	GRCh38.p7	11:65966602	CAAGATTCTCCCTCC[C/T]TCTGGGGCTCCTGCC	9092
rs770434728	snp	A/G	5.21001e-05	0.00510366	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65976698	GCCAACGGTGGCTCC[A/G]AATCTGACGGGGAGG	9092
rs770439069	snp	C/T	1.68738e-05	0.00290458	intron-variant	SART1	GRCh38.p7	11:65967227	TGCCTTTCTGTGGCC[C/T]CCGCTCCATGTCTCG	9092
rs770467917	snp	A/C			intron-variant	SART1	GRCh38.p7	11:65973373	AGATGTAGATAAGAC[A/C]GGCAGTTCACAGAAG	9092
rs770583180	snp	A/G	5.34345e-05	0.0051686	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65967684	TTTCCCCCAGAGGAA[A/G]GTGGAGCTCCACCGC	9092
rs770607849	snp	A/G	1.76899e-05	0.00297399	intron-variant	SART1	GRCh38.p7	11:65977141	CTTGGGTGGGCTTGG[A/G]TGCTGCTGCAGGTGC	9092
rs770672660	snp	C/T	1.67105e-05	0.0028905	intron-variant	SART1	GRCh38.p7	11:65977556	CTCACAACCCCTCCA[C/T]CCCTAGGGCTGCTGG	9092
rs770684733	snp	C/T	1.79677e-05	0.00299725	intron-variant	SART1	GRCh38.p7	11:65964158	CTCCCTTGTTTCTAC[C/T]TTGTTTTTCTAAGAG	9092
rs770725801	snp	C/G			intron-variant	SART1	GRCh38.p7	11:65962548	TGGTAGAGAAATGAG[C/G]GAGTAAGATAGACAG	9092
rs770772730	snp	C/T	1.68638e-05	0.00290373	intron-variant, missense	SART1	GRCh38.p7	11:65964058	AGCTCCTGAGCCATG[C/T]TTCTTCTTGTTCCAG	9092
rs770774415	snp	G/T			missense, utr-variant-5-prime, nc-transcript-variant	SART1	GRCh38.p7	11:65964531	AAACTCCGGGCAAAG[G/T]TGGGGCTGAAACCCT	9092
rs770875008	snp	C/T	1.67368e-05	0.00289277	intron-variant	SART1	GRCh38.p7	11:65977002	TAACCACCCCCGCCA[C/T]GTGTCCCGTAGTTCT	9092
rs770912198	in-del	-/G	6.36345e-05	0.00564032	intron-variant	SART1	GRCh38.p7	11:65976783	GAGGGCCGCGCCGCT[-/G]GGGGGGTGGGCGTTT	9092
rs770951129	in-del	-/TGGTCGCCTAGTGCTTC	0.000103151	0.00718088	intron-variant	SART1	GRCh38.p7	11:65965471	CTGGGCAGCATGGGG[-/TGGTCGCCTAGTGCTTC]TGGTGGCCTGACGGC	9092
rs770962983	snp	C/T	1.65704e-05	0.00287836	intron-variant	SART1	GRCh38.p7	11:65978995	CTGCAGCCTCACGCC[C/T]CTGTTCTTCTCTGCA	9092
rs770994883	snp	A/G	8.32217e-05	0.00645011	intron-variant	SART1	GRCh38.p7	11:65966328	CCAGCCTGGGTCCCA[A/G]CCTGTACCTCTTGCC	9092
rs771071434	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65969406	AGGGTTTCTAGCCCC[A/G]TGGATCTCAGCCTGC	9092
rs771104966	snp	C/T	4.002e-05	0.00447308	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	SART1	GRCh38.p7	11:65961772	CGGGCTCGGAGTGGA[C/T]GTGCCACTATGGGGT	9092
rs771154780	snp	A/C/G	0.000117897	0.00767707	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65967502	CGCCGCCGAGTGTCC[A/C/G]AAGTGGAGGAGGAGA	9092
rs771193221	snp	C/T	0.000105037	0.00724619	intron-variant	SART1	GRCh38.p7	11:65965475	GCAGCATGGGGTGGT[C/T]GCCTAGTGCTTCTGG	9092
rs771265194	snp	C/G	1.6674e-05	0.00288734	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65966179	GAAGCCTGACTACCT[C/G]CCCTATGCCGAGGAC	9092
rs771352925	snp	A/G	3.35227e-05	0.00409393	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65966078	GTGCTGCCCCCAGGC[A/G]TGCTGCAGGAGGAGG	9092
rs771383323	snp	C/T	9.59371e-05	0.00692527	intron-variant	SART1	GRCh38.p7	11:65978570	CCCCACCCAGGGCCC[C/T]GCATCTCCTCTCATG	9092
rs771471274	snp	A/G	1.90268e-05	0.00308432	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65977875	ATACGTGGATGAGAC[A/G]GGCCGGAAACTCACA	9092
rs771564764	snp	A/G	1.73492e-05	0.00294522	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65976548	CTGGCTGGCAATCGC[A/G]AGGAGCAGGAGGAGC	9092
rs771685821	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65978452	AGGGTGCCAGCGTCT[A/G]TGCTCTTTTCCCATC	9092
rs771714797	snp	C/T	2.644e-05	0.00363583	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65966525	CAGTGGGGCCCCGGC[C/T]GGCCTCCGAATACCT	9092
rs771750427	snp	C/T	3.31884e-05	0.00407346	utr-variant-3-prime, nc-transcript-variant	SART1	GRCh38.p7	11:65979034	ATCACCAAGTGACAG[C/T]GCCCTCCCGCCCCGG	9092
rs771800383	snp	C/T			intron-variant	SART1	GRCh38.p7	11:65978591	TCCTCTCATGCCCCG[C/T]GTCCCCAGGCTTTCC	9092
rs771805072	in-del	-/AAACAA/AACAC			upstream-variant-2KB	SART1	GRCh38.p7	11:65961207	TATCTCAAGGGAAAA[-/AAACAA/AACAC]AACAAAACAAAACAA	9092
rs771823127	snp	G/T	1.66073e-05	0.00288156	intron-variant	SART1	GRCh38.p7	11:65965801	CTGCAGCAGGGGTGG[G/T]ACAGGGGACACTGGT	9092
rs771855495	snp	A/C			intron-variant	SART1	GRCh38.p7	11:65966983	GTAGGCGTCTTCCTC[A/C]GTGGGTAAGAGCAGG	9092
rs771908958	snp	A/G	1.66504e-05	0.0028853	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65965716	GGCCAAGTTACTGGA[A/G]GAGATGGACCAAGAG	9092
rs771979274	snp	A/C			intron-variant	SART1	GRCh38.p7	11:65970384	ATCAAGTTTCCCACC[A/C]GCAAAGGAGCCTTTT	9092
rs772065451	snp	C/T	1.69398e-05	0.00291026	intron-variant, utr-variant-5-prime	SART1	GRCh38.p7	11:65964054	GTTCAGCTCCTGAGC[C/T]ATGCTTCTTCTTGTT	9092
rs772103416	snp	G/T	0.00246197	0.0349989	intron-variant	SART1	GRCh38.p7	11:65978934	GTGGCTCGAGGCTGG[G/T]GGGGTAGGGTGTGGT	9092
rs772153590	snp	A/G	1.96053e-05	0.00313086	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65967586	GACATCAGTGATGAG[A/G]GTGAGGGCCCGGCCA	9092
rs772162983	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65963428	GAAGCCTTTAAGATA[A/G]AGGAGAAGGTAGGAT	9092
rs772193726	snp	C/T	3.29848e-05	0.00406095	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65967329	AGGTAGTAGTGCGGG[C/T]AGATGACTTGCTGCC	9092
rs772199927	snp	A/G			utr-variant-3-prime	SART1	GRCh38.p7	11:65980134	TAAAAAAAATTTAAA[A/G]TAATCTTGGGGTGAG	9092
rs772205136	snp	C/T			intron-variant	SART1	GRCh38.p7	11:65968248	CCACCGTGCCCAGCC[C/T]TCTATTCTGTTTAAA	9092
rs772219706	in-del	-/T	1.65427e-05	0.00287595	intron-variant	SART1	GRCh38.p7	11:65964498	AGCCCCTAACACTTG[-/T]TATCTCTTGTTGTCA	9092
rs772245677	snp	A/T	7.75765e-05	0.00622754	intron-variant	SART1	GRCh38.p7	11:65965338	CACTTTTTCCCCTCT[A/T]CAGGAAGATAAAGAC	9092
rs772251285	snp	C/T	2.485e-05	0.00352482	intron-variant	SART1	GRCh38.p7	11:65965293	GCCTCTTGAGTGGGG[C/T]GGGGAGCAGGAGCTG	9092
rs772282194	snp	C/T	8.03326e-05	0.00633718	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	SART1	GRCh38.p7	11:65961763	GGCGGCAGCCGGGCT[C/T]GGAGTGGACGTGCCA	9092
rs772405043	snp	A/G			upstream-variant-2KB	SART1	GRCh38.p7	11:65961540	CGCTTCCCTTGAGGA[A/G]CGCATGCGCAATGGG	9092
rs772448406	snp	A/G	1.74659e-05	0.0029551	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65977849	GGCTACAAACCCGAC[A/G]TTAAGATCGAATACG	9092
rs772487038	snp	C/T	1.67685e-05	0.00289551	intron-variant	SART1	GRCh38.p7	11:65966071	CTGCTCTGTGCTGCC[C/T]CCAGGCGTGCTGCAG	9092
rs772553166	snp	C/G	4.97673e-05	0.00498811	intron-variant	SART1	GRCh38.p7	11:65967434	GGCTGGGGTGGCCTG[C/G]GGACCGGTGCTCACC	9092
rs772633675	snp	G/T			intron-variant	SART1	GRCh38.p7	11:65963484	GAGTTTTTTTTTTGT[G/T]TTGTTTTGTTTTTTT	9092
rs772732834	snp	C/T	1.65345e-05	0.00287524	intron-variant	SART1	GRCh38.p7	11:65964508	CACTTGTATCTCTTG[C/T]TGTCAGCAAACTCCG	9092
rs772811001	snp	C/G			intron-variant	SART1	GRCh38.p7	11:65972699	TTGAATCTAGGAGTT[C/G]GAGGTTATAGTCAGC	9092
rs772846159	snp	A/G	1.66183e-05	0.00288251	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65965727	TGGAGGAGATGGACC[A/G]AGAGTTTGGTGTCAG	9092
rs772933100	snp	G/T			intron-variant	SART1	GRCh38.p7	11:65968239	AGGTGTGTGCCACCG[G/T]GCCCAGCCCTCTATT	9092
rs772949210	snp	A/G	1.69175e-05	0.00290834	intron-variant, missense	SART1	GRCh38.p7	11:65964055	TTCAGCTCCTGAGCC[A/G]TGCTTCTTCTTGTTC	9092
rs773035344	snp	C/G	0.00131262	0.0255849	missense, utr-variant-5-prime, nc-transcript-variant	SART1	GRCh38.p7	11:65962037	GGGAGCGCAGCCAGG[C/G]AGAGCCCTCCGAGCG	9092
rs773148100	snp	A/T	1.74793e-05	0.00295624	intron-variant	SART1	GRCh38.p7	11:65977128	AGGGCAGCCATGACT[A/T]GGGTGGGCTTGGGTG	9092
rs773279041	snp	A/G	1.76372e-05	0.00296956	upstream-variant-2KB, utr-variant-3-prime	SART1, TSGA10IP	GRCh38.p7	11:65959962	ATTAAAGGCTTTATG[A/G]CAAACACAGTATGAG	9092
rs773288477	snp	A/G	5.64477e-05	0.00531231	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65976733	CATCGGCTGGAGCAC[A/G]GTGAACCTGGACGAG	9092
rs773449255	snp	A/G	1.65504e-05	0.00287662	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65965351	CTTCAGGAAGATAAA[A/G]ACCCTAGGAGAGGAT	9092
rs773465969	snp	C/T	1.65471e-05	0.00287633	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65977773	GGCCAGGGCCATCGA[C/T]GACAAGTACAGCCGG	9092
rs773479109	snp	C/T	1.64936e-05	0.00287168	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65967336	AGTGCGGGCAGATGA[C/T]TTGCTGCCTCTCGGG	9092
rs773542340	snp	C/G			downstream-variant-500B	SART1	GRCh38.p7	11:65980191	AGTAGCCTGAAAATG[C/G]ATGGTTGGCATTGAT	9092
rs773607851	snp	A/G			upstream-variant-2KB	SART1	GRCh38.p7	11:65961586	AACCCACCCGACCCG[A/G]GACGGCGCGAATGTG	9092
rs773692464	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65975730	GACATAGTGACTCGA[A/G]CCTTCACTGAGGAGT	9092
rs773748792	snp	A/G	2.07941e-05	0.00322438	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65976432	TGGAGTCTCGCCAGC[A/G]GGGCTGGGAGGAGGA	9092
rs773752878	snp	G/T	2.30322e-05	0.00339346	intron-variant	SART1	GRCh38.p7	11:65965023	CTGGAAGGGGGCAGG[G/T]TGAGTGGCTCCCTCC	9092
rs773868561	in-del	-/GGAGGCCCGGCCTGCCACAG	4.07125e-05	0.0045116	intron-variant	SART1	GRCh38.p7	11:65977922	GGGCCTTTTGCAGGC[-/GGAGGCCCGGCCTGCCACAG]GGAGGCCAAGCCCAG	9092
rs773906078	snp	A/G			synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65965949	CATTGATTCCTTCCG[A/G]GAAGGGGAGACAATG	9092
rs773965690	snp	C/T	1.69169e-05	0.00290829	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65966439	GCAGGGCGGCACGGC[C/T]GATGGCCTGCGGGAG	9092
rs774044800	snp	A/G	4.39831e-05	0.00468931	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65976426	AGAAGCTGGAGTCTC[A/G]CCAGCGGGGCTGGGA	9092
rs774052928	snp	A/G	1.66405e-05	0.00288443	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65966402	AGCTTGAAGGGGAGC[A/G]GCCACATTCCTTCCG	9092
rs774106761	snp	A/G/T	6.67561e-05	0.00577704	intron-variant	SART1	GRCh38.p7	11:65978958	GTGTGGTGGGGAGGG[A/G/T]TGGCGTGGCCTGTGC	9092
rs774127664	snp	A/C/T	0.000284143	0.0119163	synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	SART1	GRCh38.p7	11:65961822	AGAGAAGGAGGCGGC[A/C/T]GGGACGACGGCGGCG	9092
rs774140663	snp	A/G	0.000189161	0.00972341	missense, utr-variant-5-prime, nc-transcript-variant	SART1	GRCh38.p7	11:65962000	GGGGCCGAAGCTGAG[A/G]CCCGGAGCAGCACGC	9092
rs774227257	snp	C/G	1.72427e-05	0.00293616	intron-variant	SART1	GRCh38.p7	11:65965661	TTTTCTGGTGATGCT[C/G]AGTGGCCTGAAGTCC	9092
rs774301387	snp	C/T	1.65578e-05	0.00287726	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65979021	CTGCAGGAACACCAT[C/T]ACCAAGTGACAGCGC	9092
rs774307546	snp	C/G			upstream-variant-2KB	SART1	GRCh38.p7	11:65961371	GCCCATTGTAGGAGG[C/G]AGGTGTCTACGGAAA	9092
rs774314149	snp	A/T	1.71832e-05	0.00293109	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65965140	ATGTCATCAACCCTA[A/T]GGCCTTGCGACAGCG	9092
rs774370584	snp	A/G	1.67705e-05	0.00289568	intron-variant	SART1	GRCh38.p7	11:65966284	AATGGGGGCTCTGAG[A/G]AGGTGGTGGCTCAGT	9092
rs774425094	snp	A/G	1.72776e-05	0.00293913	intron-variant	SART1	GRCh38.p7	11:65978729	GGCCCTGTGCCTGCC[A/G]GGGCAGGGGTGGCTG	9092
rs774441651	snp	A/T	1.65113e-05	0.00287322	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65967287	AGACCAAGCGGAGGG[A/T]GAAGAAAATCCGCAA	9092
rs774449793	snp	C/T			utr-variant-3-prime	SART1	GRCh38.p7	11:65980046	TGAACCTGGGAGACA[C/T]AGGCTGCAGTGGGCC	9092
rs774493573	snp	C/T	1.65844e-05	0.00287957	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65977022	CCCGTAGTTCTCTGC[C/T]TCCTCCACCACCATC	9092
rs774591944	snp	C/T	1.6656e-05	0.00288578	intron-variant	SART1	GRCh38.p7	11:65966324	GGAGCCAGCCTGGGT[C/T]CCAACCTGTACCTCT	9092
rs774756783	snp	C/T	1.65457e-05	0.00287621	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65977642	AGCCGTGTACTGCAT[C/T]GAGGATAAGATGTGA	9092
rs774778419	snp	G/T			intron-variant	SART1	GRCh38.p7	11:65968226	ATGCTAAAATTACAG[G/T]TGTGTGCCACCGTGC	9092
rs774796050	snp	A/G	1.6517e-05	0.00287372	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65965913	TGCCCGGGACCTGCA[A/G]GGCCTCACCGTGGAG	9092
rs774797688	snp	A/G	2.3886e-05	0.00345578	intron-variant	SART1	GRCh38.p7	11:65964186	GAGAGGTGGCTCTGG[A/G]GCCAGCACGGGGGAG	9092
rs774868712	snp	C/T	1.65441e-05	0.00287607	intron-variant	SART1	GRCh38.p7	11:65977753	CTAAGGCCTCCTCTG[C/T]CTCGGGCCAGGGCCA	9092
rs774953935	snp	C/T			intron-variant	SART1	GRCh38.p7	11:65963670	TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATCT	9092
rs774990309	snp	A/T	0.00020004	0.009999	intron-variant	SART1	GRCh38.p7	11:65966011	GCTGGGTGCCCTGGG[A/T]GGGGGCACAGCCTCT	9092
rs774992492	snp	C/T	0.000237126	0.0108861	intron-variant	SART1	GRCh38.p7	11:65964194	GCTCTGGGGCCAGCA[C/T]GGGGGAGGCTTTCTC	9092
rs775032550	snp	C/T			intron-variant	SART1	GRCh38.p7	11:65973128	GCAGTGAGCCGAGAT[C/T]GCACCACTGCACTCC	9092
rs775087561	snp	A/G	1.66713e-05	0.0028871	missense, utr-variant-5-prime, nc-transcript-variant	SART1	GRCh38.p7	11:65964097	TCCAAAACTAGCTCA[A/G]GCGATGCCTCCTCAC	9092
rs775166238	snp	A/G	3.30349e-05	0.00406403	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65965903	ACCTGTACAGTGCCC[A/G]GGACCTGCAGGGCCT	9092
rs775241188	snp	A/G	4.20353e-05	0.00458431	intron-variant	SART1	GRCh38.p7	11:65976795	CGCTGGGGGGTGGGC[A/G]TTTGGGGGTGCTCAA	9092
rs775290537	snp	C/T	1.91834e-05	0.00309698	intron-variant	SART1	GRCh38.p7	11:65965495	AGTGCTTCTGGTGGC[C/T]TGACGGCACTGAGGC	9092
rs775296644	snp	A/G	4.36196e-05	0.00466989	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65965364	AAGACCCTAGGAGAG[A/G]ATGACCCCTGGCTGG	9092
rs775356602	in-del	-/GAA	1.6692e-05	0.00288889	cds-indel, nc-transcript-variant	SART1	GRCh38.p7	11:65966158	AAATGTGGAGCTGCG[-/GAA]GAAGAAGCCTGACTA	9092
rs775371135	in-del	-/C			intron-variant	SART1	GRCh38.p7	11:65975430	TTTTTTTTTTTTTTT[-/C]CGAGACGGGGTTTCA	9092
rs775423889	snp	C/G			upstream-variant-2KB	SART1	GRCh38.p7	11:65961014	CCCACCCCCTACCCC[C/G]GCTCCCCACCAACCA	9092
rs775435815	snp	C/T			intron-variant	SART1	GRCh38.p7	11:65978076	CTGAGGAAGGCTGTG[C/T]CTCAGTTTGTCTCTA	9092
rs775446680	in-del	-/GGGGCCTGTGCAGGGCTGA	0.000115864	0.00761044	intron-variant	SART1	GRCh38.p7	11:65977665	AGATGTGAGTGTGGT[-/GGGGCCTGTGCAGGGCTGA]GGGGCCTGTGCCAGC	9092
rs775465245	in-del	-/A			intron-variant	SART1	GRCh38.p7	11:65972785	ACAAGATCCTGTCTC[-/A]AAAAAAAAAAAAAAA	9092
rs775466453	snp	C/T	3.34633e-05	0.0040903	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65966102	GAGGAGGAGGACGTG[C/T]TGGTGAACGTGAACC	9092
rs775494189	snp	C/T	4.11421e-05	0.00453535	intron-variant	SART1	GRCh38.p7	11:65965048	CCCTCCTCTCCCCAC[C/T]AGCCATGGGCGGGCA	9092
rs775586538	snp	C/G/T	0.000116674	0.00763707	missense, synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65966194	GCCCTATGCCGAGGA[C/G/T]GAGAGCGTGGACGAC	9092
rs775656777	snp	C/T	5.19926e-05	0.00509839	intron-variant	SART1	GRCh38.p7	11:65978728	GGGCCCTGTGCCTGC[C/T]GGGGCAGGGGTGGCT	9092
rs775666456	snp	C/G	1.8415e-05	0.00303433	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65967576	GGAGAACATGGACAT[C/G]AGTGATGAGGGTGAG	9092
rs775688212	snp	C/G	1.73453e-05	0.00294489	missense, utr-variant-5-prime, nc-transcript-variant	SART1	GRCh38.p7	11:65965124	GAGCCCGTGACAGCT[C/G]ATGTCATCAACCCTA	9092
rs775720254	snp	G/T	1.72101e-05	0.00293338	intron-variant	SART1	GRCh38.p7	11:65976648	GACCCTGGTCTTTTG[G/T]GCCCCAGGACTTTGA	9092
rs775731527	snp	C/T	3.45507e-05	0.00415622	intron-variant	SART1	GRCh38.p7	11:65976581	ATGGTGCGTCTGGGG[C/T]GGCCCCGCCCTCTGC	9092
rs775749014	in-del	-/G			intron-variant	SART1	GRCh38.p7	11:65964608	GGTTTGGGGGAAAGA[-/G]GCCATCTGAAGGGGT	9092
rs775821517	snp	C/T	1.86225e-05	0.00305138	intron-variant	SART1	GRCh38.p7	11:65978575	CCCAGGGCCCTGCAT[C/T]TCCTCTCATGCCCCG	9092
rs775895357	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65967178	CACAGAGGAACACCA[A/G]AGAAGTGTTCACCCT	9092
rs775948759	snp	C/T	3.31466e-05	0.0040709	intron-variant	SART1	GRCh38.p7	11:65965820	GGGGACACTGGTGGC[C/T]TTGCTACCGGAATCC	9092
rs776002727	snp	C/T	3.20744e-05	0.00400452	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65966543	CCTCCGAATACCTCA[C/T]GCCTGAGGAGATGGT	9092
rs776005051	snp	G/T			downstream-variant-500B	SART1	GRCh38.p7	11:65980361	CTATAGTTTGACATC[G/T]GACTCTTGATTCTGT	9092
rs776036936	snp	C/T	1.68949e-05	0.0029064	intron-variant	SART1	GRCh38.p7	11:65967222	CGACCTGCCTTTCTG[C/T]GGCCCCCGCTCCATG	9092
rs776050089	snp	G/T	0.000248602	0.0111463	missense, utr-variant-5-prime, nc-transcript-variant	SART1	GRCh38.p7	11:65962058	CCTCCGAGCGGCGCG[G/T]GAAGCGGGAGAAGCG	9092
rs776095245	snp	A/C			intron-variant	SART1	GRCh38.p7	11:65973395	TCACAGAAGAGAAAG[A/C]CTAACTCACCAGGAA	9092
rs776120129	snp	C/T			synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65978638	CTTCCATGGCAAGGG[C/T]TCAGGCAAGATGAAG	9092
rs776126979	snp	C/T	2.14392e-05	0.00327401	intron-variant	SART1	GRCh38.p7	11:65967595	GATGAGGGTGAGGGC[C/T]CGGCCAGGGGGTGGG	9092
rs776152253	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65962562	GGGAGTAAGATAGAC[A/G]GGGATGTGAACACAA	9092
rs776199470	snp	C/T	0.000185587	0.00963114	intron-variant	SART1	GRCh38.p7	11:65967229	CCTTTCTGTGGCCCC[C/T]GCTCCATGTCTCGCC	9092
rs776213370	snp	C/T	1.79499e-05	0.00299577	intron-variant	SART1	GRCh38.p7	11:65977147	TGGGCTTGGGTGCTG[C/T]TGCAGGTGCAGGCAG	9092
rs776226306	snp	A/G	1.65919e-05	0.00288022	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65965757	GCACTCTGGTGGAGG[A/G]GGAGTTCGGGCAGAG	9092
rs776387852	snp	A/G	1.65176e-05	0.00287376	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65978835	ACGCCCCTGGGCACC[A/G]TGGCCCTGCTCCAGG	9092
rs776507971	in-del	-/CTC	0.000262479	0.011453	upstream-variant-2KB, cds-indel	SART1, TSGA10IP	GRCh38.p7	11:65959852	TGAGAATGGAGCACT[-/CTC]CTCAGAGGCCCCCAA	9092
rs776510670	snp	C/T	3.32646e-05	0.00407814	intron-variant	SART1	GRCh38.p7	11:65966336	GGTCCCAACCTGTAC[C/T]TCTTGCCTTGCAGCA	9092
rs776520953	snp	C/T	5.97532e-05	0.00546562	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65967693	GAGGAAGGTGGAGCT[C/T]CACCGCCGGGGTCCC	9092
rs776634921	in-del	-/GCT			intron-variant	SART1	GRCh38.p7	11:65971423	TGGTGGGATTCATGA[-/GCT]GCTGAGGAGGGGGAT	9092
rs776673930	snp	A/G	1.70316e-05	0.00291813	intron-variant	SART1	GRCh38.p7	11:65978737	GCCTGCCGGGGCAGG[A/G]GTGGCTGGTGTGTGG	9092
rs776680047	snp	A/G	0.000166138	0.0091127	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65966383	CTGTCCAAGTATGAC[A/G]AAGAGCTTGAAGGGG	9092
rs776697375	snp	C/G	1.6623e-05	0.00288292	intron-variant	SART1	GRCh38.p7	11:65967449	GGGACCGGTGCTCAC[C/G]AGAGAGGCCTCCTTC	9092
rs776704509	snp	A/G	0.000125045	0.00790614	intron-variant	SART1	GRCh38.p7	11:65965294	CCTCTTGAGTGGGGT[A/G]GGGAGCAGGAGCTGG	9092
rs776805708	snp	A/G	3.34762e-05	0.00409108	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65966095	GCTGCAGGAGGAGGA[A/G]GACGTGCTGGTGAAC	9092
rs776882673	snp	C/T	0.000334489	0.012928	intron-variant	SART1	GRCh38.p7	11:65965036	GGGTGAGTGGCTCCC[C/T]CCTCTCCCCACCAGC	9092
rs776883774	snp	A/G	1.65244e-05	0.00287436	missense, utr-variant-5-prime, nc-transcript-variant	SART1	GRCh38.p7	11:65964550	GGCTGAAACCCTTGG[A/G]GGTTAATGCCATCAA	9092
rs776898284	snp	C/T	1.67061e-05	0.00289011	intron-variant	SART1	GRCh38.p7	11:65966025	GTGGGGGCACAGCCT[C/T]TGCTGAGTTGCGGAC	9092
rs776899553	snp	C/T	1.99686e-05	0.00315974	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	SART1	GRCh38.p7	11:65961776	CTCGGAGTGGACGTG[C/T]CACTATGGGGTCGTC	9092
rs777064291	snp	A/G			missense, nc-transcript-variant	SART1	GRCh38.p7	11:65976719	GACGGGGAGGAGAAC[A/G]TCGGCTGGAGCACGG	9092
rs777105597	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65964945	CAGGAGTGTGGGGAC[A/G]AAGTGGGAGCAGGGA	9092
rs777142426	snp	A/G	0.000112467	0.00749806	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65976462	ATGAGGATCCCGAGC[A/G]GAAGGGGGCCATCGT	9092
rs777199273	snp	A/G	5.46722e-05	0.00522811	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	SART1	GRCh38.p7	11:65965096	CCCCCTTCCAGAGGC[A/G]GGCACCAAGGAGGAG	9092
rs777282037	snp	A/G	1.73294e-05	0.00294353	intron-variant	SART1	GRCh38.p7	11:65976624	GGTGGGCTGGCTGGG[A/G]CCTGGGCCGACCCTG	9092
rs777287254	snp	C/T	1.7224e-05	0.00293457	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65976685	TGAGGAGCGCTCAGC[C/T]AACGGTGGCTCCGAA	9092
rs777419247	snp	A/G			missense, nc-transcript-variant	SART1	GRCh38.p7	11:65967727	AGGTGCTGGAGGAGG[A/G]CGAGGCGGAGCTGGA	9092
rs777425559	snp	A/T			utr-variant-3-prime, downstream-variant-500B	SART1	GRCh38.p7	11:65979696	GAAAGACAAACGGCC[A/T]CCTTGGGTGCCCAGG	9092
rs777475525	snp	A/G	9.72337e-05	0.0069719	intron-variant	SART1	GRCh38.p7	11:65966582	CCGTGCCTTATACTC[A/G]GGGTCAAGATTCTCC	9092
rs777477031	snp	A/G	1.65192e-05	0.00287391	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65967281	TTAAAAAGACCAAGC[A/G]GAGGGTGAAGAAAAT	9092
rs777477795	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65968714	CAGGTGTCTCAGGAG[A/G]AGTGACCTTAGAGTG	9092
rs777502958	snp	C/T	3.30693e-05	0.00406615	intron-variant	SART1	GRCh38.p7	11:65965869	GGGAGGTTCCTGACT[C/T]GCCGATTCTTCCCTT	9092
rs777512886	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65974847	GAGACCATCCAGGCT[A/G]GTACGGTGAAACCCC	9092
rs777564381	snp	C/T			intron-variant	SART1	GRCh38.p7	11:65976154	GCCTGGTCAGGAAGG[C/T]CCTGTAGGATGTTGG	9092
rs777592613	snp	A/G	1.6604e-05	0.00288127	intron-variant	SART1	GRCh38.p7	11:65965805	AGCAGGGGTGGTACA[A/G]GGGACACTGGTGGCC	9092
rs777698984	snp	A/G	1.77102e-05	0.0029757	intron-variant	SART1	GRCh38.p7	11:65964156	GTCTCCCTTGTTTCT[A/G]CTTTGTTTTTCTAAG	9092
rs777736721	snp	C/T	3.31115e-05	0.00406874	intron-variant	SART1	GRCh38.p7	11:65977690	CAGGGCTGAGGGGCC[C/T]GTGCCAGCTTGGAGC	9092
rs777825120	snp	C/T	1.67267e-05	0.0028919	intron-variant	SART1	GRCh38.p7	11:65967665	TGAGCAGGCATCCCC[C/T]GTGTTTCCCCCAGAG	9092
rs777836660	in-del	-/GGA	1.75296e-05	0.00296049	cds-indel, nc-transcript-variant	SART1	GRCh38.p7	11:65976709	CTCCGAATCTGACGG[-/GGA]GGAGAACATCGGCTG	9092
rs777846952	snp	A/G	1.68527e-05	0.00290277	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	SART1	GRCh38.p7	11:65961767	GCAGCCGGGCTCGGA[A/G]TGGACGTGCCACTAT	9092
rs777878875	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65972894	ATTGAGAACGTGGCC[A/G]GGCGCGATGGCTCAC	9092
rs777913850	snp	C/G	6.64319e-05	0.00576295	intron-variant	SART1	GRCh38.p7	11:65978936	GGCTCGAGGCTGGTG[C/G]GGTAGGGTGTGGTGG	9092
rs777935514	snp	C/G	3.66697e-05	0.00428176	intron-variant	SART1	GRCh38.p7	11:65965461	GGGTGAGCACCTGGG[C/G]AGCATGGGGTGGTCG	9092
rs777944294	in-del	-/TTG	1.65367e-05	0.00287543	intron-variant	SART1	GRCh38.p7	11:65964505	TAACACTTGTATCTC[-/TTG]TTGTCAGCAAACTCC	9092
rs777994573	snp	A/C			intron-variant	SART1	GRCh38.p7	11:65971955	TTGTGATAGTGTCTC[A/C]CTTTGTCACCCAGGC	9092
rs778053788	snp	C/G	6.90298e-05	0.00587453	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65967555	GCCGTCGGACGACAC[C/G]CGAGTGGAGAACATG	9092
rs778133552	snp	C/T	1.68284e-05	0.00290067	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65967497	GGGGTCGCCGCCGAG[C/T]GTCCGAAGTGGAGGA	9092
rs778139903	snp	A/C	3.33634e-05	0.00408418	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65966165	GAGCTGCGGAAGAAG[A/C]AGCCTGACTACCTGC	9092
rs778244813	snp	C/T	0.000286148	0.0119579	synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	SART1	GRCh38.p7	11:65961900	CAAAAAACACAAGCA[C/T]CGGAGTGGCGGCAGT	9092
rs778334388	snp	C/G	1.67646e-05	0.00289517	intron-variant	SART1	GRCh38.p7	11:65966058	GTGTGAATGGCCACT[C/G]CTCTGTGCTGCCCCC	9092
rs778445044	snp	A/G	1.67019e-05	0.00288975	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65966147	CGGGCAGAGAAAAAT[A/G]TGGAGCTGCGGAAGA	9092
rs778503745	snp	A/G	3.33317e-05	0.00408224	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65965713	GTAGGCCAAGTTACT[A/G]GAGGAGATGGACCAA	9092
rs778521536	snp	A/G	2.37809e-05	0.00344817	intron-variant	SART1	GRCh38.p7	11:65965006	CCTTCTGGCCCCCTG[A/G]GCTGGAAGGGGGCAG	9092
rs778562324	snp	A/G/T	9.29584e-05	0.00681693	intron-variant	SART1	GRCh38.p7	11:65978590	CTCCTCTCATGCCCC[A/G/T]CGTCCCCAGGCTTTC	9092
rs778609687	snp	A/C/G	0.000121214	0.00778428	intron-variant	SART1	GRCh38.p7	11:65966571	GGTGAGCCCTCCCGT[A/C/G]CCTTATACTCGGGGT	9092
rs778721384	snp	G/T	1.88927e-05	0.00307343			GRCh38.p7	11:65965078	ATAGCCTCACGTCTG[G/T]GCCCCCCTTCCAGAG	9092
rs778892901	snp	G/T	3.33111e-05	0.00408099	intron-variant	SART1	GRCh38.p7	11:65965798	AGGCTGCAGCAGGGG[G/T]GGTACAGGGGACACT	9092
rs778899662	snp	A/G			utr-variant-3-prime	SART1	GRCh38.p7	11:65979839	AATAATCAGCTGGGC[A/G]CAGTGGCTCATGCTT	9092
rs778969153	snp	C/G	1.70145e-05	0.00291667	intron-variant	SART1	GRCh38.p7	11:65977112	CAAAGGTAGGGAGCT[C/G]AGGGCAGCCATGACT	9092
rs778988530	snp	C/T	1.65509e-05	0.00287666	intron-variant	SART1	GRCh38.p7	11:65965333	AGCATCACTTTTTCC[C/T]CTCTTCAGGAAGATA	9092
rs779008112	snp	C/T	1.73012e-05	0.00294114	intron-variant	SART1	GRCh38.p7	11:65964252	AAAGATTGTTTAAAT[C/T]ATCTTAGCCAACAGT	9092
rs779067290	snp	A/G	1.66112e-05	0.00288189	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65966376	CTCTATCCTGTCCAA[A/G]TATGACGAAGAGCTT	9092
rs779168088	in-del	-/CT	1.65623e-05	0.00287765	intron-variant	SART1	GRCh38.p7	11:65964471	AATGCACATGGCACC[-/CT]GTGTCTTTAATAGCC	9092
rs779173387	snp	G/T			intron-variant	SART1	GRCh38.p7	11:65964179	TTTCTAAGAGAGGTG[G/T]CTCTGGGGCCAGCAC	9092
rs779181054	snp	A/C/G	0.000159134	0.00891872	upstream-variant-2KB, utr-variant-3-prime	SART1, TSGA10IP	GRCh38.p7	11:65959953	TGAGATAAAATTAAA[A/C/G]GCTTTATGGCAAACA	9092
rs779194693	snp	A/C	1.69189e-05	0.00290846	intron-variant	SART1	GRCh38.p7	11:65976993	ATGGCCTGCTAACCA[A/C]CCCCGCCACGTGTCC	9092
rs779242007	snp	G/T			intron-variant	SART1	GRCh38.p7	11:65968880	CTGCTCACATGTTCT[G/T]TGTTTGTTGATTCAT	9092
rs779256214	in-del	-/CT	4.61883e-05	0.00480542	intron-variant	SART1	GRCh38.p7	11:65967664	CTGAGCAGGCATCCC[-/CT]GTGTTTCCCCCAGAG	9092
rs779263549	snp	C/T	1.67041e-05	0.00288994	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65966419	CCACATTCCTTCCGC[C/T]TGGAGCAGGGCGGCA	9092
rs779276136	snp	A/G	1.65707e-05	0.00287838	intron-variant	SART1	GRCh38.p7	11:65967423	CGAGATGGCTGGGCT[A/G]GGGTGGCCTGGGGAC	9092
rs779285461	snp	A/G	3.36101e-05	0.00409926	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65967488	TGCGGGGACGGGGTC[A/G]CCGCCGAGTGTCCGA	9092
rs779286167	snp	C/G	4.02877e-05	0.00448801	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	SART1	GRCh38.p7	11:65961751	TTGTCTGGGCTCGGC[C/G]GCAGCCGGGCTCGGA	9092
rs779300984	snp	G/T			intron-variant	SART1	GRCh38.p7	11:65970107	CACAGTGAACACCTT[G/T]GTCCTCTAGAGTCAG	9092
rs779455477	snp	C/T			intron-variant	SART1	GRCh38.p7	11:65977223	GCTGGAGCCAGCTGT[C/T]CGGCCCAGAGCCACT	9092
rs779535644	snp	A/G			synonymous-codon, utr-variant-5-prime, nc-transcript-variant	SART1	GRCh38.p7	11:65965093	GGCCCCCCTTCCAGA[A/G]GCGGGCACCAAGGAG	9092
rs779654804	snp	C/T	0.000136402	0.00825727	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65977833	CTTCAAGGAGAAGGA[C/T]GGCTACAAACCCGAC	9092
rs779660097	snp	A/G	1.68545e-05	0.00290292	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65966436	GGAGCAGGGCGGCAC[A/G]GCTGATGGCCTGCGG	9092
rs779737046	snp	A/G	4.96307e-05	0.00498125	intron-variant	SART1	GRCh38.p7	11:65967409	ACACGGTGGTGGGGC[A/G]AGATGGCTGGGCTGG	9092
rs779752291	snp	A/G	9.94777e-05	0.00705188	intron-variant	SART1	GRCh38.p7	11:65964609	GTTTGGGGGAAAGAG[A/G]CCATCTGAAGGGGTC	9092
rs779837050	snp	C/T	1.67638e-05	0.0028951	intron-variant	SART1	GRCh38.p7	11:65966053	GACAAGTGTGAATGG[C/T]CACTGCTCTGTGCTG	9092
rs779851149	snp	C/T	8.61104e-05	0.00656108	intron-variant	SART1	GRCh38.p7	11:65977929	TTGCAGGCGGAGGCC[C/T]GGCCTGCCACAGGGA	9092
rs779853042	snp	A/G	3.02202e-05	0.00388705	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65976400	CCTCCCCCAGGTGGT[A/G]GAGATTGTGAAGAAG	9092
rs780040110	snp	C/T	6.61675e-05	0.00575147	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65966508	GGCTCAGTCCCTGAG[C/T]ACAGTGGGGCCCCGG	9092
rs780087209	snp	C/T	9.94069e-05	0.00704937	intron-variant	SART1	GRCh38.p7	11:65978997	GCAGCCTCACGCCCC[C/T]GTTCTTCTCTGCAGG	9092
rs780146802	snp	G/T	1.65403e-05	0.00287574	intron-variant	SART1	GRCh38.p7	11:65965855	GTTGGGTGCGTGGAG[G/T]GAGGTTCCTGACTCG	9092
rs780309686	snp	A/C	1.68046e-05	0.00289862	intron-variant	SART1	GRCh38.p7	11:65977544	GGGGTTGGGAGTCTC[A/C]CAACCCCTCCATCCC	9092
rs780398469	in-del	-/T	3.34185e-05	0.00408756	intron-variant	SART1	GRCh38.p7	11:65964213	GGAGGCTTTCTCACA[-/T]GAAAGTGTGCTAATC	9092
rs780442389	snp	G/T	8.85559e-05	0.00665358	intron-variant	SART1	GRCh38.p7	11:65965242	TCCTGGCCAGGGCAG[G/T]CAAGGGAAGGGCTGG	9092
rs780468069	snp	A/G	1.65381e-05	0.00287555	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65978809	TCCTGAAGAAGATGA[A/G]CTCCAGCGACACGCC	9092
rs780480222	snp	A/T	1.65479e-05	0.0028764	intron-variant	SART1	GRCh38.p7	11:65978920	GCATGAACGCGTGAG[A/T]GGCTCGAGGCTGGTG	9092
rs780513044	snp	C/G	1.66098e-05	0.00288177	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65966363	AGCAAAAACCTCGCT[C/G]TATCCTGTCCAAGTA	9092
rs780541424	in-del	-/G			upstream-variant-2KB	SART1	GRCh38.p7	11:65961485	ACTTAATGGGCTCTA[-/G]AGTCCTTCCAGTTCT	9092
rs780552395	snp	C/G/T	7.1178e-05	0.00596529	upstream-variant-2KB, utr-variant-3-prime	SART1, TSGA10IP	GRCh38.p7	11:65959943	GTGCAGTCCCTGAGA[C/G/T]AAAATTAAAGGCTTT	9092
rs780606899	snp	C/T	8.90353e-05	0.00667156	upstream-variant-2KB, missense	SART1, TSGA10IP	GRCh38.p7	11:65959821	GTGTCTTGAAGGAGC[C/T]ACAGGTCAATGGGGG	9092
rs780616584	snp	C/T			intron-variant	SART1	GRCh38.p7	11:65969833	GCTCAAGCAATTCTC[C/T]TGCCTCAGCCTCCTG	9092
rs780663568	snp	G/T			intron-variant	SART1	GRCh38.p7	11:65963072	CTGGATAAAGCCATT[G/T]GGAGTCAGTATCTGG	9092
rs780666417	snp	A/C	5.2268e-05	0.00511188	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65976702	ACGGTGGCTCCGAAT[A/C]TGACGGGGAGGAGAA	9092
rs780679628	snp	A/G	4.94833e-05	0.00497385	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65967310	ATCCGCAAGAAGGAG[A/G]AGGAGGTAGTAGTGC	9092
rs780705450	snp	A/G	7.39891e-05	0.00608187	upstream-variant-2KB, missense	SART1, TSGA10IP	GRCh38.p7	11:65959926	CCCAGCCTGGACCCG[A/G]AGTGCAGTCCCTGAG	9092
rs780724130	snp	A/C/T	2.89164e-05	0.00380228	intron-variant	SART1	GRCh38.p7	11:65965320	GCTGGGCTCCTTGAG[A/C/T]ATCACTTTTTCCCCT	9092
rs780878117	snp	A/G	1.72522e-05	0.00293697	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65976689	GAGCGCTCAGCCAAC[A/G]GTGGCTCCGAATCTG	9092
rs780882465	snp	C/T	9.91965e-05	0.0070419	intron-variant	SART1	GRCh38.p7	11:65977714	TTGGAGCTTCGGGAC[C/T]ACAGCAGGCGGCAGC	9092
rs780893385	snp	C/T	1.65214e-05	0.0028741	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65965891	TCTTCCCTTAGGACC[C/T]GTACAGTGCCCGGGA	9092
rs780901269	snp	C/T	3.31307e-05	0.00406992	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65965973	GACAATGATTCTTAC[C/T]CTCAAGGACAAAGGT	9092
rs780905507	snp	C/G			intron-variant	SART1	GRCh38.p7	11:65963177	TGTTAGTAGTAGGCA[C/G]AGAAAGATGTTACCA	9092
rs780957371	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65977173	GGCAGGGCCCCCTCC[A/G]GTCCCCTCTGCTGCC	9092
rs780965331	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65964588	GAGTATGGGGCTGAG[A/G]ATAGGGTTTGGGGGA	9092
rs781018378	snp	G/T	1.79696e-05	0.00299741	intron-variant	SART1	GRCh38.p7	11:65964159	TCCCTTGTTTCTACT[G/T]TGTTTTTCTAAGAGA	9092
rs781047225	snp	C/G			intron-variant	SART1	GRCh38.p7	11:65976268	AGGCGGCAGATAGCA[C/G]CTGGGCCTGCATGGG	9092
rs781108511	in-del	-/A			intron-variant	SART1	GRCh38.p7	11:65974788	GTCTGTAACCCCAAC[-/A]ACTTTGGGAGGCCAA	9092
rs781274033	in-del	-/GGAGATGAGCACCGGGCTC	5.8957e-05	0.00542909	intron-variant	SART1	GRCh38.p7	11:65976814	GGGGGTGCTCAAGCT[-/GGAGATGAGCACCGGGCTC]GGTGTCCAGAGCCTC	9092
rs781327073	snp	C/G	1.69135e-05	0.002908	intron-variant	SART1	GRCh38.p7	11:65977106	TCAGAACAAAGGTAG[C/G]GAGCTCAGGGCAGCC	9092
rs781385225	snp	A/C	1.67399e-05	0.00289304	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65965703	TCCCTGTCCCGTAGG[A/C]CAAGTTACTGGAGGA	9092
rs781440821	snp	A/G	0.000135428	0.00822774	intron-variant	SART1	GRCh38.p7	11:65977531	CTGTGGCTCTCGAGG[A/G]GTTGGGAGTCTCACA	9092
rs781471797	snp	C/T	1.68052e-05	0.00289867	intron-variant	SART1	GRCh38.p7	11:65966279	TCGGGAATGGGGGCT[C/T]TGAGGAGGTGGTGGC	9092
rs781480710	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65972957	CGGGCGGATCACGAG[A/G]TCAGGAGATGAGACC	9092
rs781559975	snp	C/T	5.00113e-05	0.00500031	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65966180	AAGCCTGACTACCTG[C/T]CCTATGCCGAGGACG	9092
rs781576973	snp	A/G	3.14639e-05	0.00396622	intron-variant, utr-variant-5-prime	SART1	GRCh38.p7	11:65964017	GCAGCTGGAGCCAAC[A/G]ATGCTGGCTTCTTGG	9092
rs781635200	snp	C/G	3.16992e-05	0.00398103	intron-variant	SART1	GRCh38.p7	11:65967629	GGCAGGGACAGGAGC[C/G]GCGGGTTGGAGGAGA	9092
rs781659134	snp	C/T	1.7164e-05	0.00292945	synonymous-codon, nc-transcript-variant	SART1	GRCh38.p7	11:65965202	AAGGAGAAGCGCCTG[C/T]TGAACCAAAAGCTGG	9092
rs781758790	snp	C/T	1.65902e-05	0.00288008	intron-variant	SART1	GRCh38.p7	11:65978780	CCCTTTCTGAGTGGC[C/T]CCGACCCCTCAGCTC	9092
rs781780853	snp	C/T	4.99788e-05	0.00499869	missense, nc-transcript-variant	SART1	GRCh38.p7	11:65978688	AGCTGGACGAGGAGG[C/T]GGTGGGTGCCCTTGG	9092
rs796070352	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65966646	CTGAGAAGACAGGGC[A/G]AGTATTTGTGTTCAC	9092
rs796155259	snp	G/T			intron-variant	SART1	GRCh38.p7	11:65971542	GGATGGTGGGATTCA[G/T]GAGCTGAGGAGGGGG	9092
rs796231641	snp	C/T			intron-variant	SART1	GRCh38.p7	11:65962419	GGCTTCTGTTTTCCT[C/T]AGTTGTCTGGTACAA	9092
rs796393739	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65970612	AGGCAGCCCATGGCC[A/G]ATTGTTCTGGTGTTT	9092
rs796888757	snp	A/G			intron-variant	SART1	GRCh38.p7	11:65972214	ATTCTGAAATTGGAT[A/G]AAGTAGGGGCATTGT	9092
rs796934463	in-del	-/T			intron-variant	SART1	GRCh38.p7	11:65970629	TTGTTCTGGTGTTTT[-/T]CCAGTGAAGAGGTGG	9092

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