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

SPTAN1

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs13581	snp	A/C	0.0121415	0.0769634	downstream-variant-500B, utr-variant-3-prime	SPTAN1, WDR34	GRCh38.p7	9:128633739	CACCCGCCTCCCGGG[A/C]CCCCTCAGGCCGCCA	6709
rs945829	snp	A/G	0.00597247	0.0543191	intron-variant	SPTAN1	GRCh38.p7	9:128577619	TGTCAGGTATCACCT[A/G]CAAATGCAAATCACT	6709
rs945830	snp	C/T	0.0170251	0.090679	intron-variant	SPTAN1	GRCh38.p7	9:128599633	aagcaatcctcccac[C/T]tcagcctcccaggta	6709
rs945831	snp	C/T	0.0208818	0.100024	SPTAN1	9	allele_origin=T(germline)/C(germline)	9:128600082	TTTCTTTGAATAGGA[C/T]GAAACTGATTCCAAG	6709
rs945832	snp	C/T	0.0573587	0.15934	intron-variant	SPTAN1	GRCh38.p7	9:128559022	CAATTACAGGAGACA[C/T]CAAAAAACATTATGG	6709
rs945833	snp	A/G	0.0569829	0.158885	intron-variant	SPTAN1	GRCh38.p7	9:128558792	ATGTCAGCTCAGCTC[A/G]GCCTGGGCGTGCCAC	6709
rs945834	snp	C/G	0.39979	0.200158	intron-variant	SPTAN1	GRCh38.p7	9:128558260	TTCAGCAAGTAATGC[C/G]AATCTCAGGGGGATA	6709
rs945835	snp	C/T	0.0603597	0.1629	intron-variant	SPTAN1	GRCh38.p7	9:128557268	TCAGCAAGTTGAATG[C/T]ACTGGATGTAAGAGA	6709
rs953665	snp	C/G	0.475348	0.108251	intron-variant	SPTAN1	GRCh38.p7	9:128619649	agatgaggtcattag[C/G]gtggaccctaatcca	6709
rs953666	snp	C/G	0.4628	0.13121	intron-variant	SPTAN1	GRCh38.p7	9:128619583	GTGAATAGACACACA[C/G]AGTGATGCCAAGTGA	6709
rs1048236	snp	C/T	0	0	SPTAN1	9	allele_origin=T(germline)/C(germline)	9:128605330	CAGCAGAGCGCCTGA[C/T]CCAGTCCCATCCCGA	6709
rs1129922	snp	A/G			missense	SPTAN1	GRCh38.p7	9:128584297	GACCGAATTGATGGC[A/G]TCACCATTCAGGCCC	6709
rs1129924	snp	A/T			missense	SPTAN1	GRCh38.p7	9:128612226	ACAGGGATCAAGGAC[A/T]TTGACTTCTGGCTGT	6709
rs1337555	snp	A/C			intron-variant, upstream-variant-2KB	SPTAN1	GRCh38.p7	9:128554056	TTGACCTTTCAAAAT[A/C]TAAGACATTAGTTAG	6709
rs1415568	snp	A/G	0.00813715	0.0632642	SPTAN1	9	allele_origin=G(germline)/A(germline)	9:128613422	TTATGGCAAAGACCT[A/G]GCTTCTGTGAACAAC	6709
rs1572914	snp	A/G	0.394721	0.203852	intron-variant	SPTAN1	GRCh38.p7	9:128627265	CCCCAAAGATGAGAG[A/G]AGGAGGCTGGGAGAC	6709
rs1803171	snp	G/T			utr-variant-3-prime, downstream-variant-500B	SPTAN1, WDR34	GRCh38.p7	9:128633490	ACTAACCCGCTTCCG[G/T]TCCAGTCACAATCAT	6709
rs1890101	snp	A/C					GRCh38.p7	9:128559474	GTGTATGGTGCTGTT[A/C]TGCCTCCTATCACAG	6709
rs1890102	snp	C/T	0.00358779	0.0422022			GRCh38.p7	9:128554295	TATCAGAGAATCAGT[C/T]ACTAGGCTGATGGTT	6709
rs1890103	snp	C/T	0.0583345	0.161527			GRCh38.p7	9:128578360	GTTATTCACAGGTGT[C/T]TCTCATCATGAGGAT	6709
rs1890104	snp	A/T	0.434976	0.168179			GRCh38.p7	9:128578531	ATTGATCCTTTGTGA[A/T]GTAAAAAGTATTTGT	6709
rs1890105	snp	C/T	0.0667028	0.170006			GRCh38.p7	9:128578595	CAGCACTTTGGAAGG[C/T]CGAGGCGGGTGGATC	6709
rs1984180	snp	C/T			intron-variant	SPTAN1	GRCh38.p7	9:128563004	atatatatatatata[C/T]atatatatatacaca	6709
rs1984181	snp	C/T			intron-variant	SPTAN1	GRCh38.p7	9:128562992	atatatatatatata[C/T]acatacatgtatata	6709
rs1984182	snp	C/T			intron-variant	SPTAN1	GRCh38.p7	9:128562990	atatatatatataca[C/T]atacatgtatatata	6709
rs1984183	snp	C/T			intron-variant	SPTAN1	GRCh38.p7	9:128562986	atatatatacacata[C/T]atgtatatatatatt	6709
rs1984184	snp	A/G	0.0573587	0.15934	intron-variant	SPTAN1	GRCh38.p7	9:128562887	AGCTCCACCTCCTGG[A/G]TTCACGCCATTCTCC	6709
rs1984185	snp	A/G	0.0573587	0.15934	intron-variant	SPTAN1	GRCh38.p7	9:128564351	TTGAACCCGGGATGC[A/G]GAGGTTTCAATGAGC	6709
rs1984186	snp	C/T	0.190205	0.242744	intron-variant	SPTAN1	GRCh38.p7	9:128564436	aaaaaaaaaaaaaat[C/T]agccagtcatggtgg	6709
rs1999831	snp	A/G	0.0569829	0.158885	intron-variant	SPTAN1	GRCh38.p7	9:128565764	TTCCAGGGTAACACA[A/G]TTTTATACCTTTTAT	6709
rs2050629	snp	A/G	0.0569829	0.158885	intron-variant	SPTAN1	GRCh38.p7	9:128558761	ATTCCTTCCACAACC[A/G]AGGCTGCATGCTGCA	6709
rs2050630	snp	G/T	0.0603597	0.1629	intron-variant	SPTAN1	GRCh38.p7	9:128556301	CTAAATTTTTTTTTT[G/T]TGAAAAAGGTCCGAC	6709
rs2065951	snp	C/T	0.0298908	0.118541	intron-variant	SPTAN1	GRCh38.p7	9:128611326	aatagaaaaattagc[C/T]gggtgtgatgtcatg	6709
rs2095668	snp	A/G	0.151001	0.229563	intron-variant	SPTAN1	GRCh38.p7	9:128589337	tctgtcacccaggct[A/G]gagtgcagtggcacg	6709
rs2152833	snp	C/T	0.471578	0.115772	intron-variant	SPTAN1	GRCh38.p7	9:128569041	CCTTAAGAAGTTACC[C/T]GAATCCTGCCTTTGT	6709
rs2184932	snp	A/G	0.474544	0.10991	intron-variant	SPTAN1	GRCh38.p7	9:128628369	CTGGGGGCTCAGGCA[A/G]GGTACAGTAAGTCCA	6709
rs2227862	snp	C/T	0.330265	0.236765	SPTAN1	9	allele_origin=G(germline)/T(germline)/C(germline)	9:128617688	CGGCCGGGACCTAAC[C/T]GGCGTGCAGAACCTG	6709
rs2227863	snp	A/G	9.88484e-05	0.00702954	missense	SPTAN1	GRCh38.p7	9:128578178	TGAAAGCCCTCATCA[A/G]TGCAGATGAGCTTGC	6709
rs2227864	snp	C/T	0.312265	0.242122	SPTAN1	9	allele_origin=G(germline)/T(germline)/C(germline)	9:128598471	GGAGTCTGAAGGTCT[C/T]ATGGCAGAGGAGGTG	6709
rs2227865	snp	A/G	0.0134005	0.0807506	SPTAN1	9	allele_origin=G(germline)/A(germline)	9:128594259	GTTGTTCCGTGAAGC[A/G]AATGAACTACAGCAA	6709
rs2228951	snp	C/T	0.0031742	0.0397118	SPTAN1	9	allele_origin=T(germline)/C(germline)	9:128608195	GGCCTTCTTGAATAC[C/T]GAAGACAAAGGAGAC	6709
rs2228952	snp	A/C/T	0.0146655	0.0843685	SPTAN1, WDR34	9	allele_origin=T(germline)/C(germline)	9:128633289	CCGCGAGCTCCCCAC[A/C/T]GCGTTCGACTACGTG	6709
rs2275257	snp	C/G/T	0.0295035	0.117819	intron-variant	SPTAN1	GRCh38.p7	9:128566561	AGGGGAATGGATGGC[C/G/T]GTTTTTAATAAAGAA	6709
rs2275258	snp	A/G	0.0345262	0.126772	intron-variant	SPTAN1	GRCh38.p7	9:128576719	CTTGTGATTCTCTTC[A/G]GAGTGGTGATTTGCT	6709
rs2275259	snp	A/G	0.0345262	0.126772	intron-variant	SPTAN1	GRCh38.p7	9:128582048	ACATGCTATCTCGTT[A/G]AAGACATAATACAAC	6709
rs2297767	snp	C/T	0.0905309	0.192535	intron-variant	SPTAN1	GRCh38.p7	9:128575023	CTGAGACAGAAATGC[C/T]GTGAACTCAACCTCT	6709
rs2297768	snp	C/T	0.471004	0.116864	intron-variant	SPTAN1	GRCh38.p7	9:128575110	AAGCTAACATGGCTC[C/T]GTCCCTAATGTGTCT	6709
rs2297769	snp	A/C	0.02845	0.115836	SPTAN1	9	allele_origin=A(germline)/C(germline)	9:128575382	GCTTCTCACAACATT[A/C]TTATGTTAACTTTTT	6709
rs2297770	snp	A/G	0.0345262	0.126772	intron-variant	SPTAN1	GRCh38.p7	9:128575398	TTATGTTAACTTTTT[A/G]GTATATTCAGGATAA	6709
rs2297771	snp	A/G	0.458545	0.137872	intron-variant	SPTAN1	GRCh38.p7	9:128575564	GGAAGGGCAGAGTTC[A/G]TTTGATCTGTTTCCT	6709
rs3737308	snp	A/G	0.33004	0.236841	SPTAN1	9	allele_origin=G(germline)/A(germline)	9:128626364	AGAGACTGAGTTGGC[A/G]GAGTCGCCAGGGCTG	6709
rs3750332	snp	C/G	0.440333	0.16209	intron-variant	SPTAN1	GRCh38.p7	9:128617870	CAGGTTTGGACTGAG[C/G]GGTCATGAACACTTT	6709
rs3750333	snp	G/T	0.045811	0.144246	SPTAN1	9	allele_origin=G(germline)/T(germline)	9:128617719	GTTCTGCTTCCAGCC[G/T]CTTGTGCTTCTTCCT	6709
rs3763599	snp	A/G	0.372391	0.217992	intron-variant	SPTAN1	GRCh38.p7	9:128569171	GTGAATTTAACATTT[A/G]TAAGTGGCAGTGAGA	6709
rs3793450	snp	C/G	0.00755907	0.0610114	intron-variant	SPTAN1	GRCh38.p7	9:128604651	AGCCACCACGCCCAG[C/G]CTAAAAAAATTTATT	6709
rs3814530	snp	A/G	0.139903	0.224452	intron-variant	SPTAN1	GRCh38.p7	9:128591710	GCTTAGGCGTGTCCT[A/G]AGGCTCCTGGAGCCC	6709
rs3814531	snp	A/G	0.0345262	0.126772	intron-variant	SPTAN1	GRCh38.p7	9:128600312	GAGTGTCTGTCAAAT[A/G]CTCAGTACAGTTAGG	6709
rs3818829	snp	A/G	0.00119737	0.0244387	intron-variant	SPTAN1	GRCh38.p7	9:128608795	TCACCCAAAATAACT[A/G]TCCTTTTCTCAAGAC	6709
rs4240431	snp	A/G	0.0520825	0.152737	intron-variant	SPTAN1	GRCh38.p7	9:128584200	TCCTCTCAGGAATGG[A/G]AAAAAGACCTTATCA	6709
rs4307429	snp	A/G	0.0176395	0.0922421	SPTAN1	9	allele_origin=G(germline)/A(germline)	9:128588767	TAGATGACTCAGCGC[A/G]GACGTGTTTTTACCA	6709
rs4384085	snp	A/G	0.00358779	0.0422022	intron-variant	SPTAN1	GRCh38.p7	9:128582299	TGATATCTGACTGGT[A/G]ACATCAAGCAAAATC	6709
rs4395990	snp	C/G	0.45762	0.139261	intron-variant	SPTAN1	GRCh38.p7	9:128568240	GCTTTAGGTACAATC[C/G]CTGCCTGGCAGGCCC	6709
rs4506330	snp	A/T	0.458775	0.137524	intron-variant	SPTAN1	GRCh38.p7	9:128562132	TTGTTTTTTATATTT[A/T]TTATTTTTTTGACAG	6709
rs4560891	snp	C/T	0.0569829	0.158885	intron-variant	SPTAN1	GRCh38.p7	9:128563321	CTCAGGAGGCTGAGG[C/T]GGGAGGATCGCTGGA	6709
rs4836615	snp	A/G	0.0178853	0.0928588	SPTAN1	9	allele_origin=G(germline)/A(germline)	9:128584886	TTGGTGCTGCTCCTC[A/G]TGTCTCCCCTTCTTG	6709
rs4837277	snp	G/T	0.104859	0.203554	intron-variant	SPTAN1	GRCh38.p7	9:128561587	agaatggcatgaacc[G/T]gggaggcggagcttg	6709
rs4837278	snp	A/G	0.0283406	0.115616	intron-variant	SPTAN1	GRCh38.p7	9:128561620	gtgagccgaaattgc[A/G]ccactgcactccagc	6709
rs4837279	snp	A/G	0.458315	0.13822	intron-variant	SPTAN1	GRCh38.p7	9:128567804	TTGCTCTTATTGCCC[A/G]AGTTGGAGTGCAATG	6709
rs4837280	snp	A/G	0.0584853	0.160693	intron-variant	SPTAN1	GRCh38.p7	9:128578027	TAGACATTTGAGAAC[A/G]TAGAATTCAGAGCTT	6709
rs4837281	snp	C/T	0.0581099	0.160244	intron-variant	SPTAN1	GRCh38.p7	9:128578566	ccaggcacggtggct[C/T]atgtctgtaatccca	6709
rs4837282	snp	C/T	0.0581099	0.160244	intron-variant	SPTAN1	GRCh38.p7	9:128578596	agcactttggaaggc[C/T]gaggcgggtggatca	6709
rs4837283	snp	A/G	0.0905309	0.192535	intron-variant	SPTAN1	GRCh38.p7	9:128578679	actaaaaatgcaaca[A/G]ttagctggtcatggt	6709
rs4837284	snp	C/T	0.328505	0.237354	SPTAN1	9	allele_origin=T(germline)/C(germline)	9:128584890	TGCTGCTCCTCGTGT[C/T]TCCCCTTCTTGCCGA	6709
rs4837285	snp	A/G	0.0955749	0.196603	intron-variant	SPTAN1	GRCh38.p7	9:128587166	tcacgactccctaca[A/G]ctttgacctcctgtg	6709
rs4837286	snp	A/G	0.201418	0.245234	intron-variant	SPTAN1	GRCh38.p7	9:128587833	ATTTACAGAGTTTAA[A/G]ATAAGatttatttat	6709
rs4837287	snp	A/C	0.0955749	0.196603	intron-variant	SPTAN1	GRCh38.p7	9:128587926	cctcggctcactgca[A/C]cctccgcctcctggg	6709
rs4837288	snp	G/T	0.00358779	0.0422022	intron-variant	SPTAN1	GRCh38.p7	9:128601973	AACTTGGTCATTGAT[G/T]ATATGAATGGGCAAC	6709
rs4837289	snp	A/G	0.473909	0.111197	intron-variant	SPTAN1	GRCh38.p7	9:128603791	CCTGGTCAAGAGCCT[A/G]CCAGTTCTCAACAGT	6709
rs4837290	snp	C/T	0.0614824	0.164198	intron-variant	SPTAN1	GRCh38.p7	9:128618715	GTCTCGATCTCCTGA[C/T]CTCGTGATCTGCCCG	6709
rs5900805	in-del	-/T			intron-variant	SPTAN1	GRCh38.p7	9:128556479	TGTTTTGAGTCATAG[-/T]AACAATAAGGAACTT	6709
rs5900806	in-del	-/TAAA			intron-variant	SPTAN1	GRCh38.p7	9:128564588	CAAAAACAAATAAAT[-/TAAA]AAATAAATAAAAATC	6709
rs5900808	in-del	-/A	0.0923359	0.194016	intron-variant	SPTAN1	GRCh38.p7	9:128582329	CTCAAAAGTTATGAG[-/A]AAAAATGTCATCACC	6709
rs5900810	in-del	-/TTG/TTT	0	0	intron-variant	SPTAN1	GRCh38.p7	9:128588328	TTTTTTTTTTTTTTT[-/TTG/TTT]GAGATGGAGTTTCAC	6709
rs5900811	in-del	-/A			intron-variant	SPTAN1	GRCh38.p7	9:128599686	ACAAAGCACAGCTCT[-/A]AAAAAAAAAAAAAAA	6709
rs6478836	snp	C/T	0.444444	0.157135	intron-variant	SPTAN1	GRCh38.p7	9:128555623	AATTTGCAAAGCCTT[C/T]TTTTTTTTTTTTTTT	6709
rs6478837	snp	C/T	0.444444	0.157135	intron-variant	SPTAN1	GRCh38.p7	9:128555624	ATTTGCAAAGCCTTT[C/T]TTTTTTTTTTTTTTT	6709
rs6478838	snp	A/G	0.0452528	0.143452	intron-variant	SPTAN1	GRCh38.p7	9:128555792	TCCTAGATATTTGGA[A/G]AAAATAATCTGAAAA	6709
rs6478841	snp	C/G	0.199873	0.244923	intron-variant	SPTAN1	GRCh38.p7	9:128603297	GAATTGTGGTTTTTA[C/G]CATTCTTTTTTCACT	6709
rs6478842	snp	C/T	0.0581099	0.160244	intron-variant	SPTAN1	GRCh38.p7	9:128607118	AAACTGGATCAAATG[C/T]ATGCCCAGGCCTAGG	6709
rs7019666	snp	C/G	0.0581099	0.160244	intron-variant	SPTAN1	GRCh38.p7	9:128580393	GTTTTGAAGTATCTT[C/G]GAGTATAAAATTGCC	6709
rs7021150	snp	A/T	0	0	utr-variant-3-prime, downstream-variant-500B	SPTAN1, WDR34	GRCh38.p7	9:128633419	GTGCTCTCACTTTCC[A/T]CTGTAACCTTAAGCC	6709
rs7023384	snp	A/G	0.0287284	0.116357	intron-variant	SPTAN1	GRCh38.p7	9:128563957	CAACCAACATTTCTT[A/G]ATGACCTCTGTATGC	6709
rs7024498	snp	C/G	0.0175809	0.0920943	SPTAN1	9	allele_origin=G(germline)/C(germline)	9:128611886	CAGGGAGGAAGATGA[C/G]CACCGTCACTGTCAA	6709
rs7026966	snp	A/G	0.0581099	0.160244	intron-variant	SPTAN1	GRCh38.p7	9:128587434	TTGTCCCAAAAGATG[A/G]GAATCCTGAAAAACT	6709
rs7027388	snp	A/G	0.0962929	0.197165	intron-variant	SPTAN1	GRCh38.p7	9:128587494	GCAGGAGGTGATTAC[A/G]TCATTGTGCAACTGA	6709
rs7027510	snp	C/T	0.367297	0.220775	intron-variant	SPTAN1	GRCh38.p7	9:128578672	catctctactaaaaa[C/T]gcaacagttagctgg	6709
rs7028880	snp	A/G	0.0298908	0.118541	intron-variant	SPTAN1	GRCh38.p7	9:128605718	CAAAAACggccaggc[A/G]cagtggctcacgtct	6709
rs7031524	snp	C/T	0.0581099	0.160244	intron-variant	SPTAN1	GRCh38.p7	9:128579363	gacaGAGCCCTGGAA[C/T]GAAAGAGAGCTCAGA	6709
rs7032787	snp	C/T			intron-variant	SPTAN1	GRCh38.p7	9:128616990	cgcctataatcccaa[C/T]actttgggagaccga	6709
rs7032911	snp	A/G	0.0905309	0.192535	intron-variant	SPTAN1	GRCh38.p7	9:128576321	ACTCAGGCTGACAAG[A/G]CAGGATCACTTGAGA	6709
rs7033129	snp	C/T	0.0588605	0.161139	intron-variant	SPTAN1	GRCh38.p7	9:128576425	CAAACTCTTGAGCCC[C/T]GAAAATTATGTTTAT	6709
rs7036199	snp	G/T	0.0923359	0.194016	intron-variant	SPTAN1	GRCh38.p7	9:128580573	CCACTCAGTTGACAT[G/T]TCTTAGTGGAGAGTC	6709
rs7038602	snp	C/T	0.383246	0.211531	intron-variant	SPTAN1	GRCh38.p7	9:128626936	CCTCTTGCCTGAGCC[C/T]CTTGAATAACTGGGA	6709
rs7039373	snp	A/G	0.0923359	0.194016	intron-variant	SPTAN1	GRCh38.p7	9:128573062	AGGAGTGACATCTCA[A/G]TCATGGGTGGATCCC	6709
rs7040186	snp	A/G	0.0569829	0.158885	intron-variant	SPTAN1	GRCh38.p7	9:128560474	caaactccgcctccc[A/G]ggctcaagggattct	6709
rs7040737	snp	A/T	0.0133515	0.080607	SPTAN1	9	allele_origin=T(germline)/A(germline)	9:128581755	GGAATAGGACATTAT[A/T]CTGAACACTTTGTTT	6709
rs7042918	snp	A/G	0.458545	0.137872	intron-variant	SPTAN1	GRCh38.p7	9:128573394	TTTCACAGAAGGTCC[A/G]AAGTTTTTTCTATCA	6709
rs7042981	snp	A/C	0.0573587	0.15934	intron-variant	SPTAN1	GRCh38.p7	9:128566243	TTGTATTTTTAGTAG[A/C]GACGGTGTTTCACCT	6709
rs7043450	snp	A/C	0.0923359	0.194016	intron-variant	SPTAN1	GRCh38.p7	9:128573841	tcactgcaagctcca[A/C]ctccctggggtcaag	6709
rs7043517	snp	A/G	0.243347	0.249911	intron-variant	SPTAN1	GRCh38.p7	9:128573648	ttttagtagagacgg[A/G]tttcaccatgttggc	6709
rs7043563	snp	C/G	0.457504	0.139435	intron-variant	SPTAN1	GRCh38.p7	9:128573846	gcaagctccaactcc[C/G]tggggtcaagtgatt	6709
rs7043580	snp	A/G	0.0923359	0.194016	intron-variant	SPTAN1	GRCh38.p7	9:128573955	agatggggtttcacc[A/G]tgctggccagactgg	6709
rs7043692	snp	A/G	0.0923359	0.194016	intron-variant	SPTAN1	GRCh38.p7	9:128574023	ctcccaaagtgctgg[A/G]attacaggcatgagc	6709
rs7045233	snp	A/G	0.0569829	0.158885	intron-variant	SPTAN1	GRCh38.p7	9:128562028	TAAGATGAATGATAG[A/G]GGTGGGTGGTCAGGG	6709
rs7046238	snp	A/G	0.367297	0.220775	intron-variant	SPTAN1	GRCh38.p7	9:128579390	CAGACCCATGTGAAT[A/G]TGTGGAACCTTGACA	6709
rs7047416	snp	G/T	0.476574	0.105661	intron-variant	SPTAN1	GRCh38.p7	9:128574371	TAAATGAAATATAAA[G/T]ATATTATTAATAATA	6709
rs7357662	snp	C/T	0.181022	0.240296	intron-variant	SPTAN1	GRCh38.p7	9:128608477	CAGGAAAAAAAAATA[C/T]TATCAAAGGGATGGA	6709
rs7470824	snp	G/T			intron-variant	SPTAN1	GRCh38.p7	9:128597835	tttgtatttttagta[G/T]agacggggtttcacc	6709
rs7846845	snp	A/G	0.0955749	0.196603	intron-variant	SPTAN1	GRCh38.p7	9:128585408	AGTAAGTGAAACCAA[A/G]TAGGAAAAGAGCTGA	6709
rs7850861	snp	A/T	0	0	intron-variant	SPTAN1	GRCh38.p7	9:128607426	AGAAATTCGGACTTT[A/T]AAAAAAATAACAAGA	6709
rs7852794	snp	G/T	0.0573587	0.15934	intron-variant	SPTAN1	GRCh38.p7	9:128630663	cctcccaaatagctg[G/T]actacagatgtgtgc	6709
rs7857728	snp	A/C	0.347444	0.230228	intron-variant	SPTAN1	GRCh38.p7	9:128628193	GCGATTCCAAGGGCT[A/C]ACTTTGGGTAGGGAA	6709
rs7857827	snp	A/G	0.0205058	0.0991586	intron-variant	SPTAN1	GRCh38.p7	9:128628162	AAGCCAGGGGGAGCC[A/G]TCCTTGCCTCACTGG	6709
rs7864187	snp	A/C	0.303597	0.244187	SPTAN1	9	allele_origin=A(germline)/C(germline)	9:128617946	AGACAGAAGCACCAG[A/C]AGAGCTACCTGCTGT	6709
rs7866175	snp	A/G	0.0488877	0.148505	SPTAN1	9	allele_origin=G(germline)/A(germline)	9:128630274	TCATTCTGAGCTCTC[A/G]GCCAGCTGGGAGCAG	6709
rs7866931	snp	A/G	0.0569829	0.158885	intron-variant	SPTAN1	GRCh38.p7	9:128560169	gctcactgcaacctc[A/G]gcctcccgggttctg	6709
rs7867498	snp	C/T	0.470715	0.117409	intron-variant	SPTAN1	GRCh38.p7	9:128590589	AGGCGTGGTGGTTCA[C/T]GCCTATAATATCAGC	6709
rs7868827	snp	C/T	0.0170251	0.090679	intron-variant	SPTAN1	GRCh38.p7	9:128599391	ctgcccacctcagct[C/T]cccagagtgctggga	6709
rs7868835	snp	C/T	0.0611083	0.163768	intron-variant	SPTAN1	GRCh38.p7	9:128599426	AGACGTGAGCCACCA[C/T]GCCCAGCCCAGAAAT	6709
rs7870109	snp	C/T	0.424037	0.179474	intron-variant	SPTAN1	GRCh38.p7	9:128596307	ttcgagacagagtct[C/T]tctctgttgcccagg	6709
rs7870291	snp	A/G	0.0581099	0.160244	intron-variant	SPTAN1	GRCh38.p7	9:128596566	caggcgtgagccacc[A/G]cgcccggccTAATAT	6709
rs7870448	snp	A/G	0.425123	0.178415	intron-variant	SPTAN1	GRCh38.p7	9:128596402	ctgcctcagcctccc[A/G]agtagctgggactac	6709
rs9283363	snp	A/G	0	0	intron-variant	SPTAN1	GRCh38.p7	9:128590554	ATTTATATTAAAAAA[A/G]AAAAAAAAAAAAAAG	6709
rs9695753	snp	C/T	0.471004	0.116864	intron-variant	SPTAN1	GRCh38.p7	9:128586504	CTTCTCACTCACCTT[C/T]AACCGTTAACATTTG	6709
rs9695765	snp	C/G	0.0955749	0.196603	intron-variant	SPTAN1	GRCh38.p7	9:128586783	ACCTAGCTCTTACCA[C/G]TCTTCACAAAAACTA	6709
rs9696395	snp	A/G	0.0581099	0.160244	intron-variant	SPTAN1	GRCh38.p7	9:128567312	TTTTTGTTTTTTGAG[A/G]CAGAGTTGCGCTCAT	6709
rs10115510	snp	C/T	0.0444908	0.142359	intron-variant	SPTAN1	GRCh38.p7	9:128629506	AAGGGTAGGTTGGGG[C/T]GAATGTGGGTACAGG	6709
rs10115709	snp	A/C	0.0158469	0.0875917	intron-variant	SPTAN1	GRCh38.p7	9:128596209	TCCTTTTTATTGCTG[A/C]ATAATATTTCACTGT	6709
rs10117607	snp	A/G			intron-variant	SPTAN1	GRCh38.p7	9:128563028	tatatatatatatat[A/G]tatatatTTTATTAC	6709
rs10122634	snp	A/T	0.00557542	0.0525036	intron-variant	SPTAN1	GRCh38.p7	9:128623843	gtaatcccagcactt[A/T]gggaagccgaggtgg	6709
rs10123457	snp	A/C	0.00119737	0.0244387	intron-variant	SPTAN1	GRCh38.p7	9:128603703	ACCTGTGACATATCT[A/C]ACTCTATTGGGTCCA	6709
rs10124446	snp	A/G	0.0399052	0.1355	intron-variant	SPTAN1	GRCh38.p7	9:128629284	TAACCTGCCGCCCTC[A/G]GCTGCTTGGGAAGGA	6709
rs10125752	snp	A/C	0.124444	0.216185	intron-variant	SPTAN1	GRCh38.p7	9:128581493	aaaaaaaaaaacaaa[A/C]AAAAAAAACAAACCT	6709
rs10283603	snp	C/T	0	0	intron-variant	SPTAN1	GRCh38.p7	9:128591866	CTAACCAGAATTTTT[C/T]TAATCATTGCCATTT	6709
rs10513498	snp	A/G	0.0614824	0.164198	intron-variant	SPTAN1	GRCh38.p7	9:128575458	AGTGAGCAAGTTTTT[A/G]TAAGCATGTCTGAGA	6709
rs10554123	in-del	-/AGA	0.47666	0.105476	upstream-variant-2KB	SPTAN1	GRCh38.p7	9:128550878	CTGTTTTCTCTACAT[-/AGA]AGATTGCAGGAAATG	6709
rs10576967	in-del	-/TAACT	0.0581099	0.160244	intron-variant, upstream-variant-2KB	SPTAN1	GRCh38.p7	9:128553402	GTGGCTCAAATCAAA[-/TAACT]TAATAGCTTAGCGTT	6709
rs10594067	in-del	-/T	0.375	0.216506	intron-variant	SPTAN1	GRCh38.p7	9:128594823	CATCATGTATGTAGC[-/T]TTTTTTTTTTTTTTT	6709
rs10600950	in-del	-/A	0.264906	0.249555	intron-variant	SPTAN1	GRCh38.p7	9:128578836	AAAAAAAAAAAAAAA[-/A]CCTTCTGAGAGGTTT	6709
rs10627038	in-del	-/T/TT/TTT	0.43978	0.162738	intron-variant	SPTAN1	GRCh38.p7	9:128588013	CCATGCCCAGCTAAA[-/T/TT/TTT]TTTTTTTTTTTTTTT	6709
rs10648319	in-del	-/AA			intron-variant	SPTAN1	GRCh38.p7	9:128561016	CAAGACCCCATCTCA[-/AA]AAAAAAAAAAAAAAA	6709
rs10669172	in-del	-/TAAA	0	0	intron-variant	SPTAN1	GRCh38.p7	9:128564599	AAATAAATAAATAAA[-/TAAA]AATCTGGTATACAAA	6709
rs10678249	in-del	-/TT			intron-variant	SPTAN1	GRCh38.p7	9:128588028	CATGCCCAGCTAAAT[-/TT]TTTTTTTTTTTTTTT	6709
rs10679469	in-del	-/T/TTT	0	0	intron-variant	SPTAN1	GRCh38.p7	9:128594450	TTTTTTTTTTTTTTT[-/T/TTT]TGAGATGGATTCTCA	6709
rs10694437	in-del	-/AA	0.0142736	0.0832652	intron-variant	SPTAN1	GRCh38.p7	9:128626781	GAGTCACGACAAGAC[-/AA]GAGCAGGATGGAGGA	6709
rs10733692	snp	A/G	0.0603597	0.1629	intron-variant	SPTAN1	GRCh38.p7	9:128557660	CAGCTGTCTCTTGGC[A/G]TTCATCAATAAGACA	6709
rs10739725	snp	G/T	0.0923359	0.194016	intron-variant	SPTAN1	GRCh38.p7	9:128572563	TCTTCTGTGGCCTCA[G/T]TTTTAATTTGAGCAG	6709
rs10739726	snp	A/G	0.0926964	0.194308	intron-variant	SPTAN1	GRCh38.p7	9:128572611	TTTACTTTCATGCTC[A/G]CAGTTACTATGGTGA	6709
rs10739727	snp	C/T	0.0839998	0.186933	intron-variant	SPTAN1	GRCh38.p7	9:128601732	ACAAAAAGCCTCCCC[C/T]CAACAACCTTTCCGT	6709
rs10760564	snp	C/T	0.375598	0.21616	intron-variant	SPTAN1	GRCh38.p7	9:128558639	ATTTTTCCTTTCTGG[C/T]GCTCTCAAAAGGCGT	6709
rs10760565	snp	A/T			intron-variant	SPTAN1	GRCh38.p7	9:128570332	TATATATATATATAT[A/T]TTTTTTTTTTTTTTT	6709
rs10760566	snp	A/C	0.017131	0.0909507	SPTAN1	9	allele_origin=A(germline)/C(germline)	9:128583939	CCAGAAGAAACATGC[A/C]CTGCTAGAGGCAGAT	6709
rs10760567	snp	A/G	0.0142736	0.0832652	intron-variant	SPTAN1	GRCh38.p7	9:128607215	CACCACATTGCCCAA[A/G]CTGATCTTGAATTCC	6709
rs10760568	snp	C/G	0.458315	0.13822	intron-variant	SPTAN1	GRCh38.p7	9:128626915	AACCTCCCAGGCTCA[C/G]GTGATCCTCTTGCCT	6709
rs10760569	snp	A/G	0.214541	0.247473	intron-variant	SPTAN1	GRCh38.p7	9:128632018	TGTTCTTGTTTTACG[A/G]GGTCTCAGGCCAGGC	6709
rs10819406	snp	C/G	0.379942	0.213577	intron-variant, upstream-variant-2KB	SPTAN1	GRCh38.p7	9:128555122	ACCAGGGCAGCATAT[C/G]TAGAAAGTAACTGCC	6709
rs10819407	snp	C/G			intron-variant	SPTAN1	GRCh38.p7	9:128561517	AAATACAAAAAATTA[C/G]CCGGGCGAGGTGGTG	6709
rs10819408	snp	C/T	0.0569829	0.158885	intron-variant	SPTAN1	GRCh38.p7	9:128562774	TCGAGACCATCCTGG[C/T]TAGCACGGTGAAACG	6709
rs10819409	snp	G/T	0.3746	0.216737	intron-variant	SPTAN1	GRCh38.p7	9:128564163	TGGTGGCTCACGCCT[G/T]TAATCTTAGCACTTT	6709
rs10819410	snp	A/C	0.369142	0.219784	intron-variant	SPTAN1	GRCh38.p7	9:128565703	CTCACCCTTTTCTTT[A/C]TGTCTTGGGATAGAC	6709
rs10819411	snp	C/T	0.398894	0.200825	intron-variant	SPTAN1	GRCh38.p7	9:128572465	AGTACTGGGACAGGC[C/T]TTGCCCTAGTTCTTT	6709
rs10819412	snp	A/G	0.470424	0.117954	intron-variant	SPTAN1	GRCh38.p7	9:128572488	AGTTCTTTCTTGAGG[A/G]TGTAAAAATGAAATA	6709
rs10819415	snp	A/G	0.0614824	0.164198	intron-variant	SPTAN1	GRCh38.p7	9:128589844	CCTCCCAAAGTGCTG[A/G]GATTACAGGCATGAG	6709
rs10819416	snp	A/G	0.0581099	0.160244	intron-variant	SPTAN1	GRCh38.p7	9:128590766	tgaggcaggggaatc[A/G]cttaaacccaggagg	6709
rs10819417	snp	C/T	0.0648419	0.167978	intron-variant	SPTAN1	GRCh38.p7	9:128590807	aatgagccaagatcg[C/T]gccactgcactccag	6709
rs10819418	snp	C/T	0.130694	0.219696	intron-variant	SPTAN1	GRCh38.p7	9:128591102	AGTCTCGCTCTGACG[C/T]CCAGGCTGGAGTGCA	6709
rs10819419	snp	A/G	0.093777	0.195178	intron-variant	SPTAN1	GRCh38.p7	9:128591265	TAGAGACGGGGTTTC[A/G]CTGTGTTGGCCAGGA	6709
rs10819420	snp	C/G	0.110727	0.207612	intron-variant	SPTAN1	GRCh38.p7	9:128591288	GGCCAGGATGGTCTC[C/G]ATCTCCTGACCTCGT	6709
rs10819421	snp	A/G	0.375598	0.21616	intron-variant	SPTAN1	GRCh38.p7	9:128596523	CCTCGTGATCCACCC[A/G]CCTCGGTCTCCCAAA	6709
rs10819422	snp	G/T	0.3746	0.216737	intron-variant	SPTAN1	GRCh38.p7	9:128602742	CCAGGTTCAAGCGAT[G/T]CTCATGCCTCAGCCT	6709
rs10819423	snp	A/G	0.434398	0.168811	intron-variant	SPTAN1	GRCh38.p7	9:128616868	ACCTGGGAAGTGGAG[A/G]TTTCAGTGAGCCAAG	6709
rs10819424	snp	C/G	0.339882	0.233284	intron-variant	SPTAN1	GRCh38.p7	9:128619663	CGCTAATGACCTCAT[C/G]TTACCTTTGCAGAGG	6709
rs10988038	snp	C/G	0.369754	0.219451	intron-variant	SPTAN1	GRCh38.p7	9:128560999	CCAGCCTGGGCAACA[C/G]AGCAAGACCCCATCT	6709
rs10988039	snp	C/T			intron-variant	SPTAN1	GRCh38.p7	9:128563009	atatatatatatata[C/T]atatatatatatata	6709
rs10988040	snp	A/C			intron-variant	SPTAN1	GRCh38.p7	9:128565309	CGTCTCAAACAAAAA[A/C]CAAAAAAAAGCCATA	6709
rs10988041	snp	A/G	0.366679	0.221102	intron-variant	SPTAN1	GRCh38.p7	9:128568355	GAAAGAAAGTCTCAT[A/G]TGTGAGTGAATATGG	6709
rs10988042	snp	A/C	0.371582	0.218444	intron-variant	SPTAN1	GRCh38.p7	9:128570282	TCATGTCTATTAGTA[A/C]CCTCTGCCCTGTTTA	6709
rs10988043	snp	A/G	0.372592	0.217879	intron-variant	SPTAN1	GRCh38.p7	9:128570499	CCCACCACCATGCCC[A/G]GCTAATTTTTGTATA	6709
rs10988044	snp	C/T	0.371987	0.218218	intron-variant	SPTAN1	GRCh38.p7	9:128570725	GGAATGGCACGATCC[C/T]GGCTCACTGCAACCT	6709
rs10988046	snp	A/G	0.372592	0.217879	intron-variant	SPTAN1	GRCh38.p7	9:128574043	CAGGCATGAGCCGCT[A/G]CACCCAGCCTCCCCT	6709
rs10988047	snp	C/T	0.000399281	0.0141238	intron-variant	SPTAN1	GRCh38.p7	9:128581120	TGTGTTTTGCCTCCT[C/T]GGGTAGTGTGCTTGT	6709
rs10988048	snp	C/T	0	0	intron-variant	SPTAN1	GRCh38.p7	9:128581204	ATTGAGCAAGCTTCT[C/T]TCAGCTCTGCCAGCA	6709
rs10988049	snp	A/G	0.471292	0.116318	intron-variant	SPTAN1	GRCh38.p7	9:128586222	CTCCTGGGCTCAAGC[A/G]ATCCTCCTGCCTCAG	6709
rs10988050	snp	C/T			intron-variant	SPTAN1	GRCh38.p7	9:128589295	TTTTTCTTTTCTTTT[C/T]TTTTTTTTTTTGAGA	6709
rs10988051	snp	C/T			intron-variant	SPTAN1	GRCh38.p7	9:128590743	gtagtcccagctact[C/T]gggaggctgaggcag	6709
rs10988052	snp	C/T	0.200182	0.244986	intron-variant	SPTAN1	GRCh38.p7	9:128590974	TGGCAGGCGGCATTG[C/T]TCTTCTGCCTGTGAC	6709
rs10988053	snp	C/T	0.368119	0.220336	intron-variant	SPTAN1	GRCh38.p7	9:128597737	cactgtaacctctgc[C/T]gcaccccggttcaag	6709
rs10988054	snp	C/G			intron-variant	SPTAN1	GRCh38.p7	9:128601015	ttgagacggagtctc[C/G]ctctgttgcccaggc	6709
rs10988055	snp	A/G	0	0	intron-variant	SPTAN1	GRCh38.p7	9:128601271	TACTGGCCCGGCTGA[A/G]GTTTTTTATGTGATA	6709
rs10988056	snp	G/T			intron-variant	SPTAN1	GRCh38.p7	9:128602222	TTTGGGTTTTTTTTG[G/T]TTTTTTTTTTTTGAG	6709
rs10988057	snp	C/T			intron-variant	SPTAN1	GRCh38.p7	9:128605812	GCCTGGCCAACATGG[C/T]GAAATGCCGTCTCTA	6709
rs10988058	snp	C/T	0.438946	0.163706	intron-variant	SPTAN1	GRCh38.p7	9:128614901	CTGTGCATGATTTTG[C/T]AACATCATGCATGGC	6709
rs10988059	snp	A/G	0.0722614	0.17581	intron-variant	SPTAN1	GRCh38.p7	9:128616640	GGTGTGGTAGCAGGC[A/G]CCTGTGGTCCCAGCT	6709
rs10988061	snp	A/T			intron-variant	SPTAN1	GRCh38.p7	9:128622766	TTATTTATTTATTTA[A/T]TTTTTAGACGGAGTC	6709
rs10988062	snp	A/G			intron-variant	SPTAN1	GRCh38.p7	9:128622963	TCACCATGTTGGTTA[A/G]GCTGGTCTCAAACTC	6709
rs11296426	snp	A/T	0	0	intron-variant	SPTAN1	GRCh38.p7	9:128606487	CATATATATATATAt[A/T]ttttttttttggggg	6709
rs11382658	in-del	-/T	0.5	0	intron-variant	SPTAN1	GRCh38.p7	9:128585015	CTGAGCCTGAATTTC[-/T]TTTTTTTTTTTTTTT	6709
rs11429372	in-del	-/A/AA	0.496483	0.0417852	intron-variant	SPTAN1	GRCh38.p7	9:128581474	CAAAAAAAAAAAAAA[-/A/AA]CAAACAAAAAAAACA	6709
rs11442134	in-del	-/T	0.00398564	0.0444627	intron-variant	SPTAN1	GRCh38.p7	9:128630625	CCTCCACCTCCCAGG[-/T]TCAAGCAATTCTCCT	6709
rs11444346	in-del	-/A			intron-variant	SPTAN1	GRCh38.p7	9:128624112	AAAAAAAAAAAAAAA[-/A]GAATTCCTAAAAGTA	6709
rs11452757	in-del	-/G			intron-variant	SPTAN1	GRCh38.p7	9:128560632	TGATCTGCCCGCCTC[-/G]GCCTCCCAAAGTATT	6709
rs11464671	in-del	-/G	0.434687	0.168495	intron-variant	SPTAN1	GRCh38.p7	9:128577886	ATGTGGGACAGGATT[-/G]GGGGCATTATAGTGA	6709
rs11543345	snp	A/G	0.00494184	0.0494621	SPTAN1	9	allele_origin=G(germline)/A(germline)	9:128624420	AGCCCAGAGAAAGGC[A/G]AAGCTGGATGAGAAC	6709
rs11543346	snp	A/G			missense	SPTAN1	GRCh38.p7	9:128624476	AGGCGGACGTGGTGG[A/G]GTCCTGGATCGGTGA	6709
rs11543347	snp	C/G/T	0.00288655	0.0378866	SPTAN1	9	allele_origin=T(germline)/C(germline)	9:128618060	TCCAGCAGCGGCTGG[C/G/T]GCAGTTTGTGGAGCA	6709
rs11543348	snp	A/G	0.0271762	0.113356	utr-variant-3-prime, downstream-variant-500B	SPTAN1, WDR34	GRCh38.p7	9:128633489	CACTAACCCGCTTCC[A/G]GTCCAGTCACAATCA	6709
rs11787928	snp	A/G	0.0356815	0.128715	intron-variant	SPTAN1	GRCh38.p7	9:128612724	tgaggtcaggagttc[A/G]agaccagcctgacca	6709
rs11789468	snp	C/T	0.428182	0.17536	intron-variant	SPTAN1	GRCh38.p7	9:128562541	GCTTGACATGAGATA[C/T]GGCTGGAGGAGACAA	6709
rs11790032	snp	C/G	0.45946	0.136478	intron-variant	SPTAN1	GRCh38.p7	9:128586161	AGTCTCACTCTTGCC[C/G]AGGCTGGACTGCAAT	6709
rs11792043	snp	C/T			intron-variant	SPTAN1	GRCh38.p7	9:128600770	ccagttcgagcaatt[C/T]tcctgcctcagcctc	6709
rs11792065	snp	A/G	9.90279e-05	0.00703592	missense	SPTAN1	GRCh38.p7	9:128579689	CAGATGAATCTGGAC[A/G]GGCACTGCTTGCTGC	6709
rs12002245	snp	G/T	0	0	intron-variant	SPTAN1	GRCh38.p7	9:128593407	GTGCTCTGATTCTTG[G/T]TAACTCATTGCTTTT	6709
rs12002404	snp	A/C	0.0150606	0.0854603	intron-variant	SPTAN1	GRCh38.p7	9:128581485	ctcacaaaaaaaaaa[A/C]aaacaaaCAAAAAAA	6709
rs12002906	snp	A/T	0.0310518	0.120672	intron-variant	SPTAN1	GRCh38.p7	9:128582100	TAATGGAAACCTCCA[A/T]ACTTCTTTAAGTTTG	6709
rs12003066	snp	C/T	0.0535932	0.154675	intron-variant	SPTAN1	GRCh38.p7	9:128630077	GCCTTGGGAGCAAGA[C/T]GAGTGGGCTCAGCCC	6709
rs12335512	snp	C/T			intron-variant	SPTAN1	GRCh38.p7	9:128578728	cagctattcaggagt[C/T]tgaggcaggagaatc	6709
rs12338869	snp	A/G			intron-variant	SPTAN1	GRCh38.p7	9:128556136	tgaggcaggagaatc[A/G]ctttaaccgaggagt	6709
rs12339787	snp	C/T	0.470618	0.117591	intron-variant	SPTAN1	GRCh38.p7	9:128590756	cttgggaggctgagg[C/T]aggggaatcacttaa	6709
rs12342313	snp	C/T	0.0111217	0.073759	intron-variant	SPTAN1	GRCh38.p7	9:128583520	CTGAATTGGGCCTCA[C/T]TGCTGAAAATCAAAG	6709
rs12347474	snp	C/T	0	0	intron-variant	SPTAN1	GRCh38.p7	9:128568264	CAGGCCCCTTCCCAT[C/T]TTAGTATTTGATGAA	6709
rs12347525	snp	C/T			intron-variant	SPTAN1	GRCh38.p7	9:128568350	CAAGTGAAAGAAAGT[C/T]TCATGTGTGAGTGAA	6709
rs12351128	snp	A/G	0.00557542	0.0525036	intron-variant	SPTAN1	GRCh38.p7	9:128604828	cctagctacttggga[A/G]gttgaggcaggagaa	6709
rs12379323	snp	G/T			intron-variant	SPTAN1	GRCh38.p7	9:128602210	TTTTTTGtttttttt[G/T]ggttttttttgtttt	6709
rs12554457	snp	G/T	0.236144	0.249616	intron-variant	SPTAN1	GRCh38.p7	9:128602287	AGTAACGTGATCTCA[G/T]CTCACTGCAACCTCT	6709
rs12684666	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	SPTAN1	GRCh38.p7	9:128553976	GAGGAACACTCAGCT[A/G]TATGAAGCCATTGAG	6709
rs12685573	snp	C/T	0.00398564	0.0444627	intron-variant	SPTAN1	GRCh38.p7	9:128593485	TTAATTTTTAGTTTT[C/T]TATTGTTTGTTGTTT	6709
rs13283766	snp	G/T			intron-variant	SPTAN1	GRCh38.p7	9:128606496	ATATATAtttttttt[G/T]tggggggggaagcgt	6709
rs13283767	snp	G/T	0.0759472	0.179459	intron-variant	SPTAN1	GRCh38.p7	9:128606497	TATATAttttttttt[G/T]ggggggggaagcgtt	6709
rs13293951	snp	C/T	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	SPTAN1	GRCh38.p7	9:128555289	AATCTGTTTTCTTCA[C/T]GATTTTGTTCCGTTT	6709
rs13296983	snp	A/C			intron-variant	SPTAN1	GRCh38.p7	9:128552921	GAGGCTCGGCGCCGC[A/C]GCTGGAATGTCACTG	6709
rs13299607	snp	G/T	0.194278	0.243711	intron-variant	SPTAN1	GRCh38.p7	9:128609393	ACCCATGGGAAGTCA[G/T]TGAGAAATATTTCAG	6709
rs13300189	snp	A/T			intron-variant	SPTAN1	GRCh38.p7	9:128623646	ttttttttttttttg[A/T]attttttagaagaga	6709
rs13300824	snp	C/T	0.0154538	0.0865337	intron-variant	SPTAN1	GRCh38.p7	9:128565455	AAAGGAATGGTGATA[C/T]GACTAAAATCAGCTC	6709
rs13301303	snp	C/T	0	0	intron-variant	SPTAN1	GRCh38.p7	9:128618325	ATGAGTCCAGAATCA[C/T]ACATGTTTCTGTATG	6709
rs13302463	snp	A/C	0.471196	0.1165	intron-variant	SPTAN1	GRCh38.p7	9:128606640	aggcatgcaccacca[A/C]gcccggctaattttg	6709
rs13302706	snp	A/G	0.401747	0.198678	intron-variant	SPTAN1	GRCh38.p7	9:128606508	tttttggggggggaa[A/G]cgtttcgcttttgtg	6709
rs13440054	snp	C/T	0.00557542	0.0525036	intron-variant	SPTAN1	GRCh38.p7	9:128558326	TTTATAAATAGCCTA[C/T]GTCTTCAGTCTCCTC	6709
rs16930515	snp	C/T	0.0452528	0.143452	intron-variant	SPTAN1	GRCh38.p7	9:128592632	GAAAAAGATCAAATA[C/T]GTGGCTAAATTGCCT	6709
rs16930539	snp	C/T	0.0115304	0.0750483	SPTAN1	9	allele_origin=T(germline)/C(germline)	9:128630314	CTCACTGTCCTTCCA[C/T]GTTTAGGTCCTGTAT	6709
rs16930544	snp	A/C	0.00466942	0.0480927	downstream-variant-500B, intron-variant	SPTAN1, WDR34	GRCh38.p7	9:128633987	CTGCACGTCACCTGC[A/C]AAGAGAGACAGATAC	6709
rs17854811	snp	C/T			synonymous-codon	SPTAN1	GRCh38.p7	9:128579711	GCTTGCTGCTGGTCA[C/T]TATGCCTCAGATGAA	6709
rs28562867	snp	C/G	0.00557542	0.0525036	intron-variant	SPTAN1	GRCh38.p7	9:128630648	ATTCTCCTGCCTCAG[C/G]CTCCCAAATAGCTGT	6709
rs28572174	snp	A/G	0	0	intron-variant	SPTAN1	GRCh38.p7	9:128602623	GGACTTTATTTATTT[A/G]TTTTTATTTGTATTT	6709
rs28605457	snp	A/G	0.0158469	0.0875917	intron-variant	SPTAN1	GRCh38.p7	9:128584193	GAAAGAATCCTCTCA[A/G]GAATGGAAAAAAGAC	6709
rs28676915	snp	G/T	0.00562002	0.0527108	SPTAN1	9	allele_origin=G(germline)/T(germline)	9:128584269	AGTCTGCTCTGTCCT[G/T]TTGCATTCCCAGGAC	6709
rs34039280	in-del	-/TC	0.00599995	0.0544424	intron-variant	SPTAN1	GRCh38.p7	9:128630527	TAGGGCTCTTCACTA[-/TC]TCTCTCTCTTTTCTT	6709
rs34068803	in-del	-/C			intron-variant	SPTAN1	GRCh38.p7	9:128572979	TTTCAAGTAAAACAT[-/C]CCACACTTGTTTCTA	6709
rs34084388	snp	A/C/T	0.0186598	0.0947755	SPTAN1	9	allele_origin=A(germline)/C(germline)	9:128584431	GAAGCAGAAGCTGGC[A/C/T]GATTCTCTGCGGTTG	6709
rs34224870	in-del	-/C			intron-variant	SPTAN1	GRCh38.p7	9:128628063	GGGCGGGCTGCACTT[-/C]CCCCTCCCACCCTTC	6709
rs34234880	snp	A/G			intron-variant	SPTAN1	GRCh38.p7	9:128563310	ACTCCTAGCTACTCA[A/G]GAGGCTGAGGTGGGA	6709
rs34239011	in-del	-/A			frameshift-variant	SPTAN1	GRCh38.p7	9:128591533	CCGGCTGCGTACGTG[-/A]AAGAAATTGGACCCC	6709
rs34301843	in-del	-/G			intron-variant	SPTAN1	GRCh38.p7	9:128565026	AGGAAGCCATAGGTC[-/G]GGGGGCAGTGGCTCA	6709
rs34384038	in-del	-/C			intron-variant	SPTAN1	GRCh38.p7	9:128621031	CTTTATTATCCTCTT[-/C]CCCCAGCTAGACTGT	6709
rs34399310	in-del	-/T	0.0988009	0.199095	intron-variant	SPTAN1	GRCh38.p7	9:128591068	ATATCATTTTGGACC[-/T]TTTTTTTTTATGAGA	6709
rs34471574	in-del	-/G			intron-variant	SPTAN1	GRCh38.p7	9:128581329	GAACTTAGCATTGCT[-/G]GGGTGCAGTGGCTCC	6709
rs34592416	in-del	-/C			intron-variant	SPTAN1	GRCh38.p7	9:128555623	ATTTGCAAAGCCTTT[-/C]TTTTTTTTTTTTTTT	6709
rs34603055	in-del	-/C			intron-variant	SPTAN1	GRCh38.p7	9:128601546	GGCAACATGGCAAAA[-/C]CCCCGGCTCTACAAA	6709
rs34619664	in-del	-/G			intron-variant	SPTAN1	GRCh38.p7	9:128602821	TGTATTTTTAGTGGA[-/G]GACGGGGTTTCACCA	6709
rs34654141	snp	A/G	0.000495205	0.0157276	SPTAN1	9	allele_origin=G(germline)/A(germline)	9:128588826	ACAAGTGGCCCCCAC[A/G]GATGATGAGACTGGG	6709
rs34708885	in-del	-/C			intron-variant	SPTAN1	GRCh38.p7	9:128593852	CTGTAGTTGCATGAG[-/C]CCCTGTGTTACTGTG	6709
rs34874862	in-del	-/CT/T/TTTTTTTTTTTTTTTTTTCAATTTTTTTTTTTTTTTTTTTTTT			intron-variant	SPTAN1	GRCh38.p7	9:128594804	CATCATGTATGTAGC[lengthTooLong]TTTTTTTTTTTTTTT	6709
rs34912157	in-del	-/A			intron-variant	SPTAN1	GRCh38.p7	9:128571586	GCGAAATTCTGTCTG[-/A]AAAAAGTAAAAAAAT	6709
rs35052615	in-del	-/C			intron-variant	SPTAN1	GRCh38.p7	9:128628102	GATGAGGAGTGTGTG[-/C]CCTTGCCCCATAGCC	6709
rs35122170	in-del	-/T			intron-variant	SPTAN1	GRCh38.p7	9:128622293	CAACGAGCCAGCTGC[-/T]TTTTTTTTTTTTTTT	6709
rs35249383	snp	A/T	0.0162398	0.0886349	intron-variant	SPTAN1	GRCh38.p7	9:128598749	TCATTAAATATTTAA[A/T]GTTTATATAGCCATT	6709
rs35259242	in-del	-/A			intron-variant	SPTAN1	GRCh38.p7	9:128556299	AGTCGGACCTTTTTC[-/A]AAAAAAAAAAAATTT	6709
rs35428472	in-del	-/C			intron-variant	SPTAN1	GRCh38.p7	9:128564758	GGATCCTGCAGTTTA[-/C]CCCATTTCAGCTGGG	6709
rs35434571	in-del	-/T	0	0	intron-variant	SPTAN1	GRCh38.p7	9:128586137	CCATTTTTCACTTGG[-/T]TTTTTTTTTTTTTTT	6709
rs35453610	in-del	-/T			intron-variant	SPTAN1	GRCh38.p7	9:128585016	TGAGCCTGAATTTCT[-/T]TTTTTTTTTTTTTTT	6709
rs35572484	in-del	-/G			intron-variant	SPTAN1	GRCh38.p7	9:128628453	ACTTTCCTGGGGTCA[-/G]GGGAGGGTAACAAGA	6709
rs35665347	snp	A/C/G	1.70003e-05	0.00291545	downstream-variant-500B, synonymous-codon	SPTAN1, WDR34	GRCh38.p7	9:128633918	AGGGCTTTCATCCTG[A/C/G]GTTTGCTTGATCAAA	6709
rs35669351	in-del	-/G			intron-variant	SPTAN1	GRCh38.p7	9:128569422	ACTGACTTTGAGGCA[-/G]GGAGTCCTGGAACTC	6709
rs35685943	in-del	-/G			intron-variant	SPTAN1	GRCh38.p7	9:128593434	TTTTTATTTTACTTT[-/G]GGGACACTTAGATTT	6709
rs35712602	in-del	-/CA	0.376394	0.215696	intron-variant	SPTAN1	GRCh38.p7	9:128595111	CACCGTGCCCGGCCT[-/CA]GTTTTTTTTTTGTTC	6709
rs35729656	snp	A/G	0.00676609	0.0577691	intron-variant	SPTAN1	GRCh38.p7	9:128615288	CACTGCCTTTTTAAG[A/G]ACATTTTTAAGTGAA	6709
rs35782171	snp	C/T	0.029116	0.117091	intron-variant	SPTAN1	GRCh38.p7	9:128628923	CTCACCTTATGGCTC[C/T]TCCCAAGCCCTGCCC	6709
rs35875935	in-del	-/T/TT/TTT	0.224709	0.248717	intron-variant	SPTAN1	GRCh38.p7	9:128586822	TTTCTTTTTTTTTTT[-/T/TT/TTT]CTGAGACAGAGTCTC	6709
rs35889477	in-del	-/AAAT			intron-variant	SPTAN1	GRCh38.p7	9:128564581	AAAAACAAATAAATA[-/AAAT]AATAAATAAAAATCT	6709
rs35924509	in-del	-/C			intron-variant	SPTAN1	GRCh38.p7	9:128619759	GGGGACACAGTTCAG[-/C]CCCATCACATACTCC	6709
rs36095073	in-del	-/A			intron-variant	SPTAN1	GRCh38.p7	9:128623010	CTGCCTCGGCCTCCC[-/A]AAAGTGCTGGGATTA	6709
rs41275898	snp	C/T	0.00517822	0.0506191	intron-variant	SPTAN1	GRCh38.p7	9:128607798	TGAGTCGGTGGTTGA[C/T]GTCAGAGTGGGCATC	6709
rs41275900	snp	A/G	0.00104643	0.02285	SPTAN1	9	allele_origin=G(germline)/A(germline)	9:128617772	TCAGGTAAGGAGGCC[A/G]CCTTCTGGCCAAGAG	6709
rs41275902	snp	A/G	0.000107521	0.00733137	intron-variant	SPTAN1	GRCh38.p7	9:128627356	CACTGCCACAGCAGC[A/G]CACAGCATCTGCCCC	6709
rs41308912	snp	C/T	0.129473	0.219028	intron-variant	SPTAN1	GRCh38.p7	9:128630243	TTGCCAGGCATTGCT[C/T]TCTCTGAGAGAAGGT	6709
rs41308920	snp	C/T	0.026375	0.111767	intron-variant	SPTAN1	GRCh38.p7	9:128619038	TGTCACCTGCTTTCT[C/T]TCTTGGCAACTGCCT	6709
rs55678119	in-del	-/TTA	0	0	intron-variant	SPTAN1	GRCh38.p7	9:128562713	TATCATTAAATATTA[-/TTA]CAAAACTTTGGGAGG	6709
rs55717386	snp	A/G	0.000195359	0.00988137	downstream-variant-500B, utr-variant-3-prime	SPTAN1, WDR34	GRCh38.p7	9:128633708	GAAACACAAGGCTCG[A/G]CACAGCGAAGGCTTG	6709
rs55869405	snp	A/G			intron-variant	SPTAN1	GRCh38.p7	9:128616136	GATCACTTCTCCAAG[A/G]AAGGAGTTGCTTTTT	6709
rs56313017	snp	C/G			intron-variant	SPTAN1	GRCh38.p7	9:128594868	AGTCTCTCTTTTGTC[C/G]CCCAGGCTGGAGTGC	6709
rs56395039	snp	A/C			intron-variant, downstream-variant-500B	SPTAN1, WDR34	GRCh38.p7	9:128633172	TTGAAGTGGGTGCAG[A/C]TGGCTCAGGCACCAG	6709
rs56870180	snp	A/G			intron-variant	SPTAN1	GRCh38.p7	9:128570483	GCTGGGATTACAGGC[A/G]CCCACCACCATGCCC	6709
rs57158260	in-del	-/A	0.5	0	intron-variant	SPTAN1	GRCh38.p7	9:128620725	CTCCGTCTCAAAAAG[-/A]AAAAAAAAAGACATG	6709
rs57225212	in-del	-/TT	0.100944	0.200705	intron-variant	SPTAN1	GRCh38.p7	9:128589592	TTTTTTTTTTTTTTT[-/TT]GAGACAATGTCTTGC	6709
rs57478806	snp	A/G			intron-variant	SPTAN1	GRCh38.p7	9:128597071	ACACTGAGGCATGAA[A/G]ATCGCTTGAACCCGG	6709
rs57541486	snp	C/T	0.00318978	0.0398085	intron-variant	SPTAN1	GRCh38.p7	9:128567123	AAACTCATTGTTTTC[C/T]TGTATTAGTGAGGGT	6709
rs57643375	in-del	-/A			intron-variant	SPTAN1	GRCh38.p7	9:128571291	AAAGAAAAAAAAAAA[-/A]GGCCAGGCACAGTGG	6709
rs57656057	snp	A/G	0.00358779	0.0422022	intron-variant	SPTAN1	GRCh38.p7	9:128607026	TTGCCTCTTCTGGAC[A/G]TGTCATATAAAAGGA	6709
rs57777140	snp	A/G	0.00953873	0.0683987	intron-variant	SPTAN1	GRCh38.p7	9:128567193	TGCTTTAAACTGATG[A/G]TTCTCAAACCTCTGC	6709
rs58062095	in-del	-/A			intron-variant	SPTAN1	GRCh38.p7	9:128561035	AAAAAAAAAAAAAAA[-/A]GAAGTGAAAGGAACT	6709
rs58097104	snp	C/T			intron-variant	SPTAN1	GRCh38.p7	9:128630475	CAGGAACCAGATGTG[C/T]TATTATTGTACCCTT	6709
rs58345852	in-del	-/T			intron-variant	SPTAN1	GRCh38.p7	9:128593721	TATATGAGGATATTT[-/T]AAAGCTCAGTGTACC	6709
rs58583132	snp	A/T	0	0	intron-variant	SPTAN1	GRCh38.p7	9:128562971	CTCCGTCTAAAAAAA[A/T]ATATATATATACATG	6709
rs58631866	snp	A/C			intron-variant	SPTAN1	GRCh38.p7	9:128557456	GTTTGTATCTGCAGT[A/C]TTTTGTGTTGCTTAA	6709
rs58956945	in-del	-/AAAAAAAAAAA	0.100588	0.200439	intron-variant	SPTAN1	GRCh38.p7	9:128624087	AATTCACTCCGTCTC[-/AAAAAAAAAAA]AAAAAAAAAAAAAAA	6709
rs59257779	in-del	-/AAAAAA/AAAAAAA	0	0	intron-variant	SPTAN1	GRCh38.p7	9:128606392	AAAAAAAAAAAAAAA[-/AAAAAA/AAAAAAA]CAAGTCTCTACTTTC	6709
rs59259018	in-del	-/GTAT			intron-variant	SPTAN1	GRCh38.p7	9:128563031	TATATATATATGTAT[-/GTAT]ATATTTTATTACAAA	6709
rs59442689	snp	A/C	0.00318978	0.0398085	intron-variant	SPTAN1	GRCh38.p7	9:128567411	ATTCTCCAGCCTCAG[A/C]CTCCCAGGTTGCTGG	6709
rs59518899	snp	C/G	0.0134861	0.0810011	intron-variant	SPTAN1	GRCh38.p7	9:128556039	AGCCTGGCCAACATA[C/G]TGAAACCCCATCTCT	6709
rs59617922	snp	C/T	0.00358779	0.0422022	intron-variant	SPTAN1	GRCh38.p7	9:128573915	GTGCGCCCCCATACC[C/T]GGCTCATTTTTGTAC	6709
rs59648185	in-del	-/T	0.0581099	0.160244	intron-variant	SPTAN1	GRCh38.p7	9:128572477	GCCTTGCCCTAGTTC[-/T]TTTCTTGAGGGTGTA	6709
rs60003572	in-del	-/GTATATATATATAT			intron-variant	SPTAN1	GRCh38.p7	9:128562995	TACATGTATGTGTAT[-/GTATATATATATAT]ATATATATATATATA	6709
rs60170037	in-del	-/AA			intron-variant	SPTAN1	GRCh38.p7	9:128578853	AAAAAAAAAAAAAAA[-/AA]CCTTCTGAGAGGTTT	6709
rs60290370	in-del	-/TTTTTTTTT			intron-variant	SPTAN1	GRCh38.p7	9:128601001	TTTTTTTTTTTTTTT[-/TTTTTTTTT]GAGACGGAGTCTCGC	6709
rs60899207	in-del	-/AT			intron-variant	SPTAN1	GRCh38.p7	9:128615115	AAAAGTTTGAATTTT[-/AT]CATTAGTAACAAACT	6709
rs61069314	snp	A/C	0.140919	0.224948	upstream-variant-2KB	SPTAN1	GRCh38.p7	9:128551675	GCCTAGTACACAAGG[A/C]AAGTTCGATTAATTG	6709
rs61089660	in-del	-/T/TT	0	0	intron-variant	SPTAN1	GRCh38.p7	9:128588029	TTTTTTTTTTTTTTT[-/T/TT]GAGATGGAGTCTTGC	6709
rs61530011	snp	A/G	0.00517822	0.0506191	intron-variant	SPTAN1	GRCh38.p7	9:128560145	CTGGAGTGCAAAGGC[A/G]TGATCTTGGCTCACT	6709
rs62584813	snp	A/G	0.0023933	0.0345097	intron-variant	SPTAN1	GRCh38.p7	9:128559838	CTCCCGGGTTCAAGC[A/G]ATTCTCCTGTCTCAG	6709
rs62584842	snp	A/C			intron-variant	SPTAN1	GRCh38.p7	9:128581395	GGAGTATCCCTTGAG[A/C]CCAGGAGCTCAAGGC	6709
rs62584843	snp	C/G	0.0310518	0.120672	intron-variant	SPTAN1	GRCh38.p7	9:128589043	CCCTGAAATGAGAAG[C/G]CTTAGAATTCAAAGA	6709
rs62584844	snp	A/G	0	0	intron-variant	SPTAN1	GRCh38.p7	9:128590571	AAAAAAAAAAAAAGG[A/G]CCAGGCGTGGTGGTT	6709
rs62586287	snp	C/T	0.45843	0.138046	intron-variant	SPTAN1	GRCh38.p7	9:128597110	GGTTGCAGTGAGCCA[C/T]GATCACGCCACTGCA	6709
rs62586288	snp	A/G	0.000798403	0.0199641	intron-variant	SPTAN1	GRCh38.p7	9:128606877	ATTTAATGTATTCAC[A/G]GTGTTGTGCAGCCAC	6709
rs62586289	snp	A/G	0.00358779	0.0422022	intron-variant	SPTAN1	GRCh38.p7	9:128616425	CCACTGCGCCTGGTC[A/G]GAAGGCTTTAAGGAA	6709
rs62586290	snp	A/C/T	0.5	0	intron-variant	SPTAN1	GRCh38.p7	9:128628573	CCCGCCCAGTCCCGG[A/C/T]AGGGACTTCTCTGCT	6709
rs66475636	in-del	-/T	0.206947	0.246265	intron-variant	SPTAN1	GRCh38.p7	9:128592278	TTTTGGTTTGTGTTC[-/T]TTTTTTTTTTTTTTG	6709
rs66578587	in-del	-/TT	0.407845	0.193868	intron-variant	SPTAN1	GRCh38.p7	9:128594805	CATCATGTATGTAGC[-/TT]TTTTTTTTTTTTTTT	6709
rs66615866	in-del	-/AG			intron-variant	SPTAN1	GRCh38.p7	9:128590553	TATTTATATTAAAAA[-/AG]AAAAAAAAAAAAAAG	6709
rs67011624	in-del	-/TGTATGTG			intron-variant	SPTAN1	GRCh38.p7	9:128562985	AAATATATATATACA[-/TGTATGTG]TATATATATATATAT	6709
rs67280704	in-del	-/AA			intron-variant	SPTAN1	GRCh38.p7	9:128626782	AGTCACGACAAGACG[-/AA]AGCAGGATGGAGGAG	6709
rs71381771	in-del	-/G/GC	0	0	intron-variant	SPTAN1	GRCh38.p7	9:128560633	GATCTGCCCGCCTCG[-/G/GC]CCTCCCAAAGTATTG	6709
rs71381772	in-del	-/AA	0	0	intron-variant	SPTAN1	GRCh38.p7	9:128561035	AAAAAAAAAAAAAAA[-/AA]GAAGTGAAAGGAACT	6709
rs71381773	in-del	-/GTATGTGTATATATATAT	0	0	intron-variant	SPTAN1	GRCh38.p7	9:128562986	TATATATATATACAT[-/GTATGTGTATATATATAT]ATATATATATATATA	6709
rs71381780	in-del	-/G	0	0	intron-variant	SPTAN1	GRCh38.p7	9:128606505	TTTTTTTGGGGGGGG[-/G]AAACGTTTCGCTTTT	6709
rs71495699	in-del	-/C	0.5	0	intron-variant	SPTAN1	GRCh38.p7	9:128606624	AGTAGCTGGGATCAC[-/C]AGGCATGCACCACCA	6709
rs71495700	in-del	-/A	0.5	0	intron-variant	SPTAN1	GRCh38.p7	9:128631789	GCGCCACTGCACTCT[-/A]AGCCTAGGCGACAGT	6709
rs71495701	in-del	-/C	0.5	0	intron-variant	SPTAN1	GRCh38.p7	9:128631792	GCCACTGCACTCTAG[-/C]CTAGGCGACAGTGAG	6709
rs71499403	snp	G/T	0.5	0	intron-variant	SPTAN1	GRCh38.p7	9:128592817	GCTATTTCTTTACTG[G/T]CATGTCACTCATGAC	6709
rs71499404	snp	G/T	0.375	0.216506	intron-variant	SPTAN1	GRCh38.p7	9:128602634	ATTTGTTTTTATTTG[G/T]ATTTTATTTATTTAT	6709
rs71923773	in-del	-/AT			intron-variant	SPTAN1	GRCh38.p7	9:128606473	TATTTTTCCCTAGAC[-/AT]ATATATATATATATT	6709
rs72214808	in-del	-/T			intron-variant	SPTAN1	GRCh38.p7	9:128557800	TAAATTAGAAATTTC[-/T]TTTTTTTTTTTTTTT	6709
rs72758805	snp	A/G	0.0023933	0.0345097	intron-variant	SPTAN1	GRCh38.p7	9:128564687	CTATAGAGAAGTGTG[A/G]TTACGTCTGAGAAGG	6709
rs72758823	snp	A/C/T	0.000798843	0.0199725	SPTAN1	9	allele_origin=T(germline)/A(germline)/C(germline)	9:128626609	GATCAAGAGCTTCCG[A/C/T]GTAGCCTCCAACCCC	6709
rs72758828	snp	C/G	0.000798403	0.0199641	intron-variant	SPTAN1	GRCh38.p7	9:128631617	GATCACTTGAGCCTA[C/G]GAATTCAAGACCAGC	6709
rs73612934	snp	G/T	0.00318978	0.0398085	intron-variant	SPTAN1	GRCh38.p7	9:128562822	TAGAAAATATTAGCC[G/T]GGCGTGATGGCAGGC	6709
rs73618492	snp	C/T	0.0603597	0.1629	intron-variant	SPTAN1	GRCh38.p7	9:128563994	TCAGGGATACAGGAC[C/T]GGACATGGTGGCTTA	6709
rs73618495	snp	A/G	0.0603597	0.1629	intron-variant	SPTAN1	GRCh38.p7	9:128564516	TGAACCAGGGAGGTC[A/G]AGGTTGCAGTGAGCC	6709
rs73618499	snp	C/T	0.00318978	0.0398085	intron-variant	SPTAN1	GRCh38.p7	9:128565810	AATAGCTGGAAGGGA[C/T]CAGCAGGCTTATCTG	6709
rs73620005	snp	A/C	0.00358779	0.0422022	intron-variant	SPTAN1	GRCh38.p7	9:128569768	ACTGTTTTGTCTCCT[A/C]CTCTTCCTTGATAAC	6709
rs73620025	snp	A/G	0.00358779	0.0422022	intron-variant	SPTAN1	GRCh38.p7	9:128575667	CGAGGGTGTGGTGGT[A/G]AATGCTAAGTTAGTA	6709
rs73620040	snp	C/G	0.00358779	0.0422022	intron-variant	SPTAN1	GRCh38.p7	9:128579103	GTACACAGATGGAAC[C/G]ATCTTCTGTGAAGGT	6709
rs73623531	snp	C/T	0.00358779	0.0422022	intron-variant	SPTAN1	GRCh38.p7	9:128609983	CTTTTGAAGATGGAA[C/T]ATCAGCTTCAGCTTT	6709
rs73623534	snp	A/G	0.00358779	0.0422022	intron-variant	SPTAN1	GRCh38.p7	9:128610177	CTATTAATACCTCCA[A/G]ATCTTCAAGGAACAC	6709
rs73623547	snp	C/T	0.00398564	0.0444627	intron-variant	SPTAN1	GRCh38.p7	9:128619384	AGAGATTTATTGCTT[C/T]TCAGTTCTGGAGGCC	6709
rs73623551	snp	C/G	0.000399281	0.0141238	intron-variant	SPTAN1	GRCh38.p7	9:128624569	TGGTTTTCTTCTGCA[C/G]AGAAGAAACTGATCA	6709
rs73623560	snp	A/G	0.5	0	intron-variant	SPTAN1	GRCh38.p7	9:128629569	CGCACCGTGTGATTC[A/G]TCCCTGCACGTAACC	6709
rs73669920	snp	A/G	0.0119091	0.0762411	intron-variant, upstream-variant-2KB	SPTAN1	GRCh38.p7	9:128555076	ACTTTAACAAGTGGG[A/G]AAATTGAGGCCCCAA	6709
rs73669921	snp	A/G	0.00199481	0.0315187	intron-variant	SPTAN1	GRCh38.p7	9:128565756	CCAGATGTTTCCAGG[A/G]TAACACAATTTTATA	6709
rs73669954	snp	G/T	0.00159617	0.0282053	intron-variant	SPTAN1	GRCh38.p7	9:128576226	ACCAAAATGTGGTTG[G/T]TAGGGAAGGATACTT	6709
rs74393024	snp	C/T			intron-variant	SPTAN1	GRCh38.p7	9:128572481	TTGCCCTAGTTCTTT[C/T]TTGAGGATGTAAAAA	6709
rs74399523	snp	A/G	0.0554779	0.157039	intron-variant	SPTAN1	GRCh38.p7	9:128622283	CAGCCTCCTGGCAAC[A/G]AGCCAGCTGCTTTTT	6709
rs74462823	snp	C/G	0.5	0	intron-variant	SPTAN1	GRCh38.p7	9:128630735	TGAGATGGAGTTTCA[C/G]TCTTGTTGCCCAGGC	6709
rs74482094	snp	A/G	0.0414363	0.137845	intron-variant	SPTAN1	GRCh38.p7	9:128609988	GAAGATGGAACATCA[A/G]CTTCAGCTTTTTCTG	6709
rs74560703	snp	A/T	0.5	0	intron-variant	SPTAN1	GRCh38.p7	9:128562133	TGTTTTTTATATTTT[A/T]TATTTTTTTGACAGG	6709
rs74565779	snp	A/G	0.0391387	0.134304	intron-variant	SPTAN1	GRCh38.p7	9:128601645	GTTTGACAAGCAAAT[A/G]AAAAACAAAAAGTAA	6709
rs74813851	snp	C/T	0.0640965	0.167152	intron-variant	SPTAN1	GRCh38.p7	9:128587463	CTTTGAAAATGATAT[C/T]AGCACTGTAAGAAGG	6709
rs74856439	snp	G/T	0.5	0	intron-variant	SPTAN1	GRCh38.p7	9:128586111	ATCCATTTTTCACTT[G/T]GTTTTTTTTTTTTTT	6709
rs74920594	snp	G/T	0.5	0	intron-variant	SPTAN1	GRCh38.p7	9:128563732	TTTTTTTTTTTTTTT[G/T]TGAGACAGGGTCTCA	6709
rs74995813	snp	G/T	0.0325976	0.123435	utr-variant-3-prime, downstream-variant-500B	SPTAN1, WDR34	GRCh38.p7	9:128633445	AAGCCTGCTTAGCTT[G/T]GAATAAGACTTAGGA	6709
rs75028792	snp	A/G	0.00161673	0.0283858	SPTAN1	9	allele_origin=G(germline)/A(germline)	9:128632704	GGCAATCCTGGACAC[A/G]GTGGATCCGAACAGG	6709
rs75053418	snp	A/G	0.0670745	0.170406	intron-variant	SPTAN1	GRCh38.p7	9:128591007	TCTGCAGGTATGGCA[A/G]GTGAGGAAGGGACTG	6709
rs75086467	snp	C/T	0.0399052	0.1355	intron-variant	SPTAN1	GRCh38.p7	9:128629707	GAGAGGAGGCTCCCT[C/T]CCTGGCTGTGTCTAG	6709
rs75119678	snp	A/G	0.00371252	0.0429241	intron-variant	SPTAN1	GRCh38.p7	9:128599081	TTCATCAGAATTGCT[A/G]TTCCTGAACCTCAGA	6709
rs75269823	snp	A/G	0.0391387	0.134304	intron-variant	SPTAN1	GRCh38.p7	9:128619902	CTGGAGGTCCTTCAC[A/G]CTCCTGCATTCAGGC	6709
rs75341829	snp	G/T	0.00159617	0.0282053	intron-variant	SPTAN1	GRCh38.p7	9:128578009	AGAATTTATATAGTT[G/T]GTTAGACATTTGAGA	6709
rs75351362	snp	A/C	0.0596104	0.162024	intron-variant	SPTAN1	GRCh38.p7	9:128568407	ACTGAATGTTGAGAA[A/C]ACTGTTGGTATGGTT	6709
rs75406910	snp	C/T	0.0558544	0.157504	intron-variant	SPTAN1	GRCh38.p7	9:128621748	AATTATCAAAAACCT[C/T]GAGGCTGTACAGGGC	6709
rs75428787	snp	A/G	0.0240643	0.107019	intron-variant	SPTAN1	GRCh38.p7	9:128559500	TACACTCGAATCCTG[A/G]AGACTGCCATCTCTT	6709
rs75433116	snp	C/T	0	0	intron-variant	SPTAN1	GRCh38.p7	9:128557802	AATTAGAAATTTCTT[C/T]TTTTTTTTTTTTTTT	6709
rs75528824	snp	A/C/G	0.00914918	0.0670815	intron-variant	SPTAN1	GRCh38.p7	9:128621900	GTGTGTCCGTGGGTC[A/C/G]GGAATTCACCAGCAA	6709
rs75537926	snp	C/G	0.0150606	0.0854603	intron-variant	SPTAN1	GRCh38.p7	9:128600279	ACTCTAAAATGTGAT[C/G]CTTAATATACAAAAG	6709
rs75593228	snp	C/T	0.0441095	0.141807	intron-variant	SPTAN1	GRCh38.p7	9:128561961	TCCTTAAAGGACTTA[C/T]GAATGTGGTAGGGAG	6709
rs75693914	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime, downstream-variant-500B	SPTAN1, WDR34	GRCh38.p7	9:128633393	GCCTTGCTGCATGTC[C/T]GCTCCTCTGTGTGCT	6709
rs75758182	snp	A/C	0.5	0	intron-variant	SPTAN1	GRCh38.p7	9:128614589	AATGAGACTACGTCT[A/C]AAAAAAAAAACAAAA	6709
rs75889464	snp	C/T	0.5	0	intron-variant	SPTAN1	GRCh38.p7	9:128560381	AAGCCACCGTGCCCG[C/T]CTTTTTTTTTTTTTT	6709
rs75915555	snp	C/G	0.5	0	intron-variant	SPTAN1	GRCh38.p7	9:128565692	CTCTTAGCCTACTCA[C/G]CCTTTTCTTTCTGTC	6709
rs75924412	snp	A/T	0.000798403	0.0199641	intron-variant	SPTAN1	GRCh38.p7	9:128603230	TAGTATAGACAAGAA[A/T]ATGACACTAATCATT	6709
rs75978579	snp	A/G	0	0	intron-variant	SPTAN1	GRCh38.p7	9:128626782	GAGTCACGACAAGAC[A/G]AGCAGGATGGAGGAG	6709
rs76011388	snp	A/G	0.0154538	0.0865337	intron-variant	SPTAN1	GRCh38.p7	9:128614957	AGTTATGCCTGTTCT[A/G]TATGTTGACACATGT	6709
rs76070860	snp	A/G	0.00676609	0.0577691	intron-variant	SPTAN1	GRCh38.p7	9:128629795	TGGTCGTGATCTCCC[A/G]GCACTCCACTTGTGT	6709
rs76156881	snp	A/T	0.0142736	0.0832652	intron-variant	SPTAN1	GRCh38.p7	9:128593533	ATTTCAGCCTTTTGT[A/T]TTTTAGTTCCCGAGG	6709
rs76196653	snp	C/T	0.067446	0.170804	intron-variant	SPTAN1	GRCh38.p7	9:128592762	TAAGCATGGCAGACC[C/T]GCCAGGAAAATGAAG	6709
rs76220061	snp	C/G/T	0.0383715	0.133092	intron-variant	SPTAN1	GRCh38.p7	9:128579411	AACCTTGACAAATGA[C/G/T]AGGTGACCTGAAAAG	6709
rs76351026	snp	A/G	0.0041911	0.0455849	intron-variant	SPTAN1	GRCh38.p7	9:128583311	ATTGAATTGTGACAT[A/G]CATGTTTGGGGAACT	6709
rs76393340	snp	C/T	0.0577344	0.159793	intron-variant	SPTAN1	GRCh38.p7	9:128617426	CAACCCTCCAGAATC[C/T]GGACACACAGCAGGG	6709
rs76483781	snp	C/T	0.0984431	0.198823	intron-variant	SPTAN1	GRCh38.p7	9:128558997	TAAGAGGGGGGAAAC[C/T]CTCACTAACCCATAA	6709
rs76501192	snp	A/G	0.00358779	0.0422022	intron-variant	SPTAN1	GRCh38.p7	9:128564930	AAGGGTAGGGGTCAC[A/G]GGTGAGAGATAATAC	6709
rs76508044	snp	C/T	0.5	0	intron-variant	SPTAN1	GRCh38.p7	9:128560383	GCCACCGTGCCCGCC[C/T]TTTTTTTTTTTTTTT	6709
rs76531514	snp	A/G	0.0577344	0.159793	intron-variant	SPTAN1	GRCh38.p7	9:128583375	TATACCCCCCAAGAA[A/G]GGTGAGGTGGATGAC	6709
rs76572364	snp	C/T	0.00279162	0.0372561	intron-variant	SPTAN1	GRCh38.p7	9:128590864	CCAATAAAAAAGAGT[C/T]CTAACTCAATGAAAG	6709
rs76587835	snp	A/C	0.100588	0.200439	intron-variant	SPTAN1	GRCh38.p7	9:128614610	AAAAACAAAAAAAAA[A/C]CACAAAAATTAATTA	6709
rs76614650	snp	A/G	0.0122245	0.0772192	intron-variant	SPTAN1	GRCh38.p7	9:128583309	CCATTGAATTGTGAC[A/G]TGCATGTTTGGGGAA	6709
rs76672103	snp	A/G	0.00199481	0.0315187	intron-variant	SPTAN1	GRCh38.p7	9:128559221	GTATAGAATTGACTC[A/G]TTCTACTTCACTGGG	6709
rs76700452	snp	C/T	0.0573587	0.15934	intron-variant	SPTAN1	GRCh38.p7	9:128553239	TGACCTTAATTTCAT[C/T]CTGCATGGCGAATCT	6709
rs76736205	snp	C/G	0	0	intron-variant	SPTAN1	GRCh38.p7	9:128621842	CTTTCTCAGCAGCAG[C/G]GAAGCCACATCCCTC	6709
rs76742194	in-del	-/TAT	0.0607341	0.163335	intron-variant	SPTAN1	GRCh38.p7	9:128562708	CCTGTTATCATTAAA[-/TAT]TATTACAAAACTTTG	6709
rs76767787	snp	C/T	0.00015075	0.00868057	synonymous-codon	SPTAN1	GRCh38.p7	9:128632249	CAGCACCGTGGGCCT[C/T]GCCCAGCAGTGGGAC	6709
rs76781152	snp	C/G	0.0391387	0.134304	intron-variant	SPTAN1	GRCh38.p7	9:128591778	CCCACAGACCTCCCT[C/G]TGTGGGTCTCAGACC	6709
rs76800933	snp	A/T	0.00199481	0.0315187	intron-variant	SPTAN1	GRCh38.p7	9:128593171	GGAACTGCCTGTCCG[A/T]GCAGCAGCTTTGGCT	6709
rs76805429	snp	A/G	0.0399052	0.1355	intron-variant	SPTAN1	GRCh38.p7	9:128553291	AAGGGTCTGAGACTG[A/G]CCGTCTCCTTTTCTT	6709
rs76935328	snp	C/T	0.078151	0.181571	intron-variant	SPTAN1	GRCh38.p7	9:128595689	AGAAAACCACATATC[C/T]GTCAAGCATTCATTT	6709
rs77074093	snp	A/G	0.0452528	0.143452	upstream-variant-2KB	SPTAN1	GRCh38.p7	9:128551043	GACAGCTTAGAAACC[A/G]TATTGCAGGTCCCAG	6709
rs77103380	snp	A/G	0.0667028	0.170006	intron-variant	SPTAN1	GRCh38.p7	9:128579364	ACAGAGCCCTGGAAT[A/G]AAAGAGAGCTCAGAC	6709
rs77117600	snp	A/G	0.029116	0.117091	intron-variant	SPTAN1	GRCh38.p7	9:128557366	CTCTTTTGGGATTCC[A/G]TAGAGAAACTGACTG	6709
rs77139835	snp	A/G	0.0182019	0.0936463	intron-variant	SPTAN1	GRCh38.p7	9:128614892	AGCTCTTACCTGTGC[A/G]TGATTTTGCAACATC	6709
rs77140770	snp	C/G			missense	SPTAN1	GRCh38.p7	9:128578211	GTGATGTGGCTGGGG[C/G]TGAAGCCCTGCTAGA	6709
rs77263873	snp	A/T	0.5	0	intron-variant	SPTAN1	GRCh38.p7	9:128590703	AAAATACAAAAAAAT[A/T]AGCTGTGCGTGGTGG	6709
rs77315490	snp	A/G	0.0418186	0.138422	intron-variant	SPTAN1	GRCh38.p7	9:128608565	CTGTTTGATTTATAC[A/G]TCACTTTGCTGTAAA	6709
rs77358650	snp	A/G	0.0112702	0.0742163	SPTAN1	9	allele_origin=G(germline)/A(germline)	9:128580928	GCCCCCAAGCTGACC[A/G]TCCTTTCCGAGGAGA	6709
rs77404988	snp	A/G	0.0569829	0.158885	intron-variant, upstream-variant-2KB	SPTAN1	GRCh38.p7	9:128553658	TTAAATGAAAAGCCT[A/G]AATAGCTCAGAAAGC	6709
rs77425677	snp	A/G	0.00438332	0.0466095	intron-variant	SPTAN1	GRCh38.p7	9:128565392	TTTTGGACTGTGGAA[A/G]AACAATAATACAACA	6709
rs77452993	snp	A/G	0.00557542	0.0525036	intron-variant	SPTAN1	GRCh38.p7	9:128556894	AGAATCAACTGGTAT[A/G]CAATTTTATGAGTGC	6709
rs77594718	snp	A/G	0.0372196	0.131242	intron-variant	SPTAN1	GRCh38.p7	9:128611491	AAGGACTTCCAGTTC[A/G]TCTACTCCTGAGCTA	6709
rs77600182	snp	C/T	0.0166325	0.0896639	intron-variant	SPTAN1	GRCh38.p7	9:128563524	CTAGTTGTGTAGCTT[C/T]AGTCAGCACATTCTT	6709
rs77645530	snp	A/G	0.029116	0.117091	intron-variant	SPTAN1	GRCh38.p7	9:128557318	CTTTGTTTTTAATAG[A/G]GACTCCTTTCAGCTT	6709
rs77723951	snp	G/T	0.5	0	intron-variant	SPTAN1	GRCh38.p7	9:128610569	TAGTTGTTTTTTTTT[G/T]GCCCCCCAAATAACA	6709
rs77733303	snp	A/G	0.0125753	0.0782911	intron-variant	SPTAN1	GRCh38.p7	9:128628081	CCTCCCACCCTTCTC[A/G]TCACCTGATGAGGAG	6709
rs77736877	snp	C/T	0.0581099	0.160244	intron-variant	SPTAN1	GRCh38.p7	9:128595511	TGTTATAAGAACTTT[C/T]CTAAGCCTAAACTAC	6709
rs77741454	snp	C/G	0.030665	0.119967	intron-variant, upstream-variant-2KB	SPTAN1	GRCh38.p7	9:128553787	GTTATTTTAGAAAAA[C/G]TTACCATCATGGCTG	6709
rs77785950	snp	C/T			intron-variant	SPTAN1	GRCh38.p7	9:128564580	GTCCTGTCTCAAAAA[C/T]AAATAAATAAATAAA	6709
rs77926333	snp	A/G	0.021333	0.101051	intron-variant	SPTAN1	GRCh38.p7	9:128617445	CACACAGCAGGGCTC[A/G]TAGATGCATAGATGG	6709
rs77947092	snp	G/T	0	0	intron-variant	SPTAN1	GRCh38.p7	9:128586115	ATTTTTCACTTGGTT[G/T]TTTTTTTTTTTTTTT	6709
rs78014314	snp	A/G	0.0539704	0.155153	intron-variant	SPTAN1	GRCh38.p7	9:128555583	TGGTGTTAAATTATC[A/G]GAAGTATTAGTAAAT	6709
rs78060503	snp	C/T	0.00279162	0.0372561	intron-variant	SPTAN1	GRCh38.p7	9:128606951	TCCTTAACTAATCAC[C/T]CCCTCTTCTCTCTTC	6709
rs78064656	snp	C/T	0.0441095	0.141807	intron-variant	SPTAN1	GRCh38.p7	9:128583642	GAGCAGAGGCTGCAA[C/T]TGATATTTTCTTTCT	6709
rs78099980	snp	C/T	0.5	0	intron-variant	SPTAN1	GRCh38.p7	9:128592279	TTTGGTTTGTGTTCT[C/T]TTTTTTTTTTTTTGA	6709
rs78117059	snp	A/G	0.00517822	0.0506191	intron-variant	SPTAN1	GRCh38.p7	9:128600343	TTGCATTGATTACCC[A/G]TGTTGGTGCAGGATA	6709
rs78157393	snp	G/T	0.5	0	intron-variant	SPTAN1	GRCh38.p7	9:128592291	TCTTTTTTTTTTTTT[G/T]TGAGACAGATTCTCG	6709
rs78197797	snp	A/G	0.00358779	0.0422022	intron-variant	SPTAN1	GRCh38.p7	9:128574981	CTAGGTGTATGTGCT[A/G]TTCTGTAACTCTGAA	6709
rs78256464	snp	A/T	0.5	0	intron-variant	SPTAN1	GRCh38.p7	9:128565153	ACGAAAAATACAAAA[A/T]TTAGCTGGGCGTGGT	6709
rs78336605	snp	A/G	0.0414363	0.137845	intron-variant	SPTAN1	GRCh38.p7	9:128568286	TTTGATGAAAAAGAG[A/G]TATTGAGAAATGGAG	6709
rs78401969	snp	A/G	0.00835141	0.0640778	intron-variant	SPTAN1	GRCh38.p7	9:128591703	GGCCGAAGCTTAGGC[A/G]TGTCCTGAGGCTCCT	6709
rs78493234	snp	A/G	0.0391387	0.134304	intron-variant	SPTAN1	GRCh38.p7	9:128598870	TGTCCTTTTGGAATT[A/G]TCTCCTGTGTTTCCA	6709
rs78527469	snp	A/G	0.0130921	0.0798413	intron-variant	SPTAN1	GRCh38.p7	9:128631777	AGTGAGCGTGATTGC[A/G]CCACTGCACTCTAGC	6709
rs78689583	snp	C/T	0.0554779	0.157039	intron-variant	SPTAN1	GRCh38.p7	9:128579182	CTCAGCAGGTATATG[C/T]GTGTGTTTCTTTTTG	6709
rs78691412	snp	C/T	0.030665	0.119967	intron-variant	SPTAN1	GRCh38.p7	9:128620259	TGCACTCCCAGGAAT[C/T]GAGTTAGCTTTGAGC	6709
rs78695294	snp	A/G	0.0581099	0.160244	intron-variant	SPTAN1	GRCh38.p7	9:128571844	TGTCCAGTCACCACT[A/G]TTTGTTTTATTTTAA	6709
rs78712556	snp	C/G	0.5	0	intron-variant	SPTAN1	GRCh38.p7	9:128600899	AACTCCTGACCTCAG[C/G]TGATCTGCCTGCCTC	6709
rs78737440	snp	A/C	0.0345262	0.126772	intron-variant	SPTAN1	GRCh38.p7	9:128601960	TCTTACGTAGCAAAA[A/C]TTGGTCATTGATGAT	6709
rs78856736	snp	C/G	0.0441095	0.141807	intron-variant	SPTAN1	GRCh38.p7	9:128603264	CTTTTAGGTATTTTT[C/G]TGTCCAACTAGCTGC	6709
rs78940490	snp	A/G	0.00636936	0.0560724	intron-variant	SPTAN1	GRCh38.p7	9:128609458	TCAGAGCCATTTAAA[A/G]GTTGCCTTCCTCATT	6709
rs78966823	snp	G/T	0.5	0	intron-variant	SPTAN1	GRCh38.p7	9:128593415	ATTCTTGGTAACTCA[G/T]TGCTTTTTTATTTTA	6709
rs79022250	in-del	-/TTA			intron-variant	SPTAN1	GRCh38.p7	9:128562712	TTATCATTAAATATT[-/TTA]AYAAAACTTTGGGAG	6709
rs79099671	snp	G/T	0.5	0	intron-variant	SPTAN1	GRCh38.p7	9:128560397	CTTTTTTTTTTTTTT[G/T]TGACACGGAGTCTAG	6709
rs79140166	snp	C/G	0.0345262	0.126772	intron-variant	SPTAN1	GRCh38.p7	9:128613054	ATATTTTGCTGTAGT[C/G]AATATCTTTGAATAT	6709
rs79176107	snp	A/G	0.0150606	0.0854603	intron-variant	SPTAN1	GRCh38.p7	9:128615445	TGCAAATGTCCACAC[A/G]GTAAAAAATAATAAT	6709
rs79206042	snp	A/T	0.5	0	intron-variant	SPTAN1	GRCh38.p7	9:128590701	CTAAAATACAAAAAA[A/T]TTAGCTGTGCGTGGT	6709
rs79268762	snp	C/T	0.0410537	0.137264	intron-variant	SPTAN1	GRCh38.p7	9:128600340	AGGTTGCATTGATTA[C/T]CCATGTTGGTGCAGG	6709
rs79569204	snp	C/T	0.00324437	0.0401454	SPTAN1	9	allele_origin=T(germline)/C(germline)	9:128618031	CGATGACAACACCAT[C/T]GGGAAAGAGGAGATC	6709
rs79604728	snp	C/G/T	0.0236746	0.106192	intron-variant	SPTAN1	GRCh38.p7	9:128568710	GAACACGGGGAACAG[C/G/T]GGGGACAAAATGCTG	6709
rs79650677	snp	A/C			missense	SPTAN1	GRCh38.p7	9:128582509	GCAACCAAGCTAATT[A/C]AGAACAACCACTATG	6709
rs79677350	snp	C/T	0.0123036	0.0774623	intron-variant	SPTAN1	GRCh38.p7	9:128575616	TGGGTGAAGCTTTTA[C/T]TGGACTGCTGAAGCT	6709
rs79726731	snp	A/G	0.0391387	0.134304	intron-variant	SPTAN1	GRCh38.p7	9:128586330	TAGAGACAGGGTCTC[A/G]CTATGTTGTCCCATC	6709
rs79728807	snp	C/T	0.0414363	0.137845	intron-variant	SPTAN1	GRCh38.p7	9:128563673	TCTGCTGCACAGCAT[C/T]TGCAACATTCAGCAT	6709
rs79811889	snp	A/G	0.030665	0.119967	intron-variant	SPTAN1	GRCh38.p7	9:128557711	ATTTTGTAGGAATCC[A/G]TTTTCAGTTGATACT	6709
rs79844555	snp	C/T	0.00119737	0.0244387	intron-variant	SPTAN1	GRCh38.p7	9:128595692	AAACCACATATCCGT[C/T]AAGCATTCATTTGCC	6709
rs79846056	snp	A/G	0.0345262	0.126772	intron-variant	SPTAN1	GRCh38.p7	9:128585407	GAGTAAGTGAAACCA[A/G]GTAGGAAAAGAGCTG	6709
rs79848175	snp	C/T	0.0566069	0.158427	intron-variant	SPTAN1	GRCh38.p7	9:128576450	GTTTATGTGCAAGAA[C/T]GCTTAACAGCCTCAT	6709
rs79940826	snp	A/G	0.0345262	0.126772	intron-variant	SPTAN1	GRCh38.p7	9:128607551	TTTTCCTGGGCAGAA[A/G]ATCTCCTTACCAGGT	6709
rs80024923	snp	A/G	0.0573587	0.15934	intron-variant	SPTAN1	GRCh38.p7	9:128571719	TGCAAGGTGGCCATT[A/G]TTTCCCTATTATGTG	6709
rs80039019	snp	C/T	0.0345262	0.126772	intron-variant	SPTAN1	GRCh38.p7	9:128595720	GCCATTCTCCCTAAC[C/T]CCAGTGGCCCACGCA	6709
rs80060491	snp	C/T	0.0414363	0.137845	intron-variant	SPTAN1	GRCh38.p7	9:128590240	AATTTAAACCTAAAC[C/T]AACTTGTGGTCTAAC	6709
rs80127562	snp	C/G	0.00993419	0.0697739	upstream-variant-2KB	SPTAN1	GRCh38.p7	9:128552113	GGCCGGGGCGCGCAG[C/G]ATCCCCAGCCAGACT	6709
rs80147558	snp	C/T	0.5	0	intron-variant	SPTAN1	GRCh38.p7	9:128560384	CCACCGTGCCCGCCT[C/T]TTTTTTTTTTTTTTG	6709
rs80154358	snp	A/G	0.00914312	0.0669923	intron-variant	SPTAN1	GRCh38.p7	9:128603977	GGGTGTTGGGAGGCA[A/G]CAGACTCGCTGGGAT	6709
rs80173027	snp	A/G	0.0240643	0.107019	intron-variant	SPTAN1	GRCh38.p7	9:128568706	GGAGGAACACGGGGA[A/G]CAGCGGGGACAAAAT	6709
rs80262973	snp	A/G	0.0112985	0.0743075	intron-variant	SPTAN1	GRCh38.p7	9:128582883	TGCCATGTAGCACTC[A/G]ATTAGTAAGCTAAAC	6709
rs80314885	snp	A/G	0.0399052	0.1355	intron-variant, upstream-variant-2KB	SPTAN1	GRCh38.p7	9:128554002	TTGAGTCAAGGTTCC[A/G]ACTCCTTAACTAGTC	6709
rs80326848	snp	A/G	0.0337553	0.125452	intron-variant	SPTAN1	GRCh38.p7	9:128619735	AGTTAGGACTTCACC[A/G]TCTCTTGAGGGGGAC	6709
rs111285612	in-del	-/T	0.43655	0.16643	intron-variant	SPTAN1	GRCh38.p7	9:128599482	GGTTTTTTTTTTTTT[-/T]CGGTCTTTTGTTTGT	6709
rs111309840	snp	G/T	0.0718919	0.175435	intron-variant	SPTAN1	GRCh38.p7	9:128619678	CTTACCTTTGCAGAG[G/T]ACATTTGCAAAGATC	6709
rs111395012	snp	C/T	0.0554779	0.157039	intron-variant	SPTAN1	GRCh38.p7	9:128573784	TTTGAGACGGAGTCT[C/T]GCTCTGTCGCCCAGA	6709
rs111400127	snp	C/T			intron-variant	SPTAN1	GRCh38.p7	9:128578107	TCCTTTGGTTTTCCC[C/T]AGGCTTCAACGCTTC	6709
rs111402431	snp	A/C	0.5	0	intron-variant	SPTAN1	GRCh38.p7	9:128598726	GGGCTTCTGTCTTCT[A/C]CGTAAGCTCATTAAA	6709
rs111471756	snp	C/T	0.5	0	intron-variant	SPTAN1	GRCh38.p7	9:128600179	TGAAATATGTCCTTT[C/T]CTGGTGTGCCTTTCT	6709
rs111493195	snp	C/T	0.0154538	0.0865337	intron-variant	SPTAN1	GRCh38.p7	9:128580197	CACATTCCTATAGTC[C/T]GAGCTACTTGAGTTC	6709
rs111521146	in-del	-/TTTA/TTTATTTA	0.0908951	0.196824	intron-variant	SPTAN1	GRCh38.p7	9:128622737	TGACTTGTAGTATGG[-/TTTA/TTTATTTA]TTTATTTATTTATTT	6709
rs111559353	in-del	-/AAAT	0.5	0	intron-variant	SPTAN1	GRCh38.p7	9:128564580	TCCTGTCTCAAAAAC[-/AAAT]AAATAAATAAATAAA	6709
rs111563269	snp	A/C	0.039522	0.134904	intron-variant	SPTAN1	GRCh38.p7	9:128619458	CCTGTAGGGGAGGAT[A/C]TTTCCTTGCCTCTTC	6709
rs111578866	snp	A/G	0.00358779	0.0422022	intron-variant	SPTAN1	GRCh38.p7	9:128565189	AGGCCTGTAGTCCCC[A/G]CTACTCGGGAGGCTG	6709
rs111691651	in-del	-/T	0.443732	0.158012	intron-variant	SPTAN1	GRCh38.p7	9:128623960	GGTGGTGTTCGCCTA[-/T]TAGTCCCAGCTACTC	6709
rs111807264	snp	C/G	0.5	0	intron-variant	SPTAN1	GRCh38.p7	9:128608510	ACAAATGTGTGGGTA[C/G]GTAAGGGAATAATGA	6709
rs111846527	snp	A/T	0.0150606	0.0854603	intron-variant	SPTAN1	GRCh38.p7	9:128605632	GCGAATTGCTTGAAC[A/T]CAGGAGCCGGAGACC	6709
rs111924243	snp	C/T	0.5	0	intron-variant	SPTAN1	GRCh38.p7	9:128603711	CATATCTCACTCTAT[C/T]GGGTCCAAGCATGTC	6709
rs112047036	snp	A/G	0.0150606	0.0854603	intron-variant	SPTAN1	GRCh38.p7	9:128579542	CATTTTAGATGTCAT[A/G]GTCTGGCTTATAATG	6709
rs112060874	in-del	-/TAGCAAAACT	0.5	0	intron-variant	SPTAN1	GRCh38.p7	9:128601952	TTCCCTTTTCTTACG[-/TAGCAAAACT]TGGTCATTGATGATA	6709
rs112064644	snp	A/G	0.0410537	0.137264	intron-variant	SPTAN1	GRCh38.p7	9:128598754	AAATATTTAATGTTT[A/G]TATAGCCATTAACTA	6709
rs112092840	snp	C/T	0.443464	0.15834	intron-variant	SPTAN1	GRCh38.p7	9:128623856	TTTGGGAAGCCGAGG[C/T]GGGCAAATCACCTGA	6709
rs112101146	snp	A/G	0.5	0	intron-variant	SPTAN1	GRCh38.p7	9:128603226	CCTGTAGTATAGACA[A/G]GAAAATGACACTAAT	6709
rs112116933	snp	C/T	0.5	0	intron-variant	SPTAN1	GRCh38.p7	9:128603870	GCACAGTCTCAGTAA[C/T]GCAGTGAGCGGCTTC	6709
rs112129457	snp	C/T	0.00119737	0.0244387	intron-variant	SPTAN1	GRCh38.p7	9:128591393	TTAAAACAACGCTCT[C/T]GTGTGTGTGTATACA	6709
rs112132867	snp	C/G	0.0410537	0.137264	intron-variant	SPTAN1	GRCh38.p7	9:128596085	CTGAGCTCAGGCCGT[C/G]TGCCCAGCTTGCCCT	6709
rs112177902	in-del	-/A	0.5	0	intron-variant	SPTAN1	GRCh38.p7	9:128564421	AAGAGTCCTTCTCAG[-/A]AAAAAAAAAAAAATT	6709
rs112276354	snp	A/C/T	0	0	intron-variant	SPTAN1	GRCh38.p7	9:128632805	TGCTTCCCCCGCTCC[A/C/T]AGAGATGGCCATGTC	6709
rs112344009	snp	C/T	0	0	intron-variant	SPTAN1	GRCh38.p7	9:128620891	TGGATGACAAAGGGT[C/T]TGACCCTTCCCAAAG	6709
rs112366038	snp	C/T	0.0154538	0.0865337	intron-variant	SPTAN1	GRCh38.p7	9:128591930	TTTTCAGATACTCTA[C/T]GCCCCTACAGCTCTG	6709
rs112372253	snp	C/G	0.0055786	0.0525184	intron-variant	SPTAN1	GRCh38.p7	9:128632541	CGGCAGCAGGGCTGC[C/G]TGCTGAGCCGCCCTC	6709
rs112416122	in-del	-/T	0.5	0	intron-variant	SPTAN1	GRCh38.p7	9:128627563	TAAGCCCTGGGGAGC[-/T]TTCCAGCCCCAAGGA	6709
rs112462793	snp	A/G	0.0150606	0.0854603	intron-variant	SPTAN1	GRCh38.p7	9:128617843	CCTTGCGCTTATTTC[A/G]CTGAGGTCCCTAAAG	6709
rs112466837	snp	A/G	0.039522	0.134904	upstream-variant-2KB	SPTAN1	GRCh38.p7	9:128552213	AGACGACTGTCCGCA[A/G]GGCGGGCGGTGGCGG	6709
rs112479500	snp	C/T	0.0119091	0.0762411	intron-variant	SPTAN1	GRCh38.p7	9:128598095	CTGGGATTACAGGCA[C/T]GGACCCCCACACCCA	6709
rs112504385	snp	C/T	0.00874735	0.0655527	intron-variant, upstream-variant-2KB	SPTAN1	GRCh38.p7	9:128553805	ACCATCATGGCTGTT[C/T]GGGAAGAACAGGAGA	6709
rs112532901	snp	C/T	0.0588605	0.161139	intron-variant	SPTAN1	GRCh38.p7	9:128562163	GCTGGAGTGCAGTGA[C/T]GCGATCTGGGCTCAT	6709
rs112538732	snp	C/T	0.5	0	intron-variant	SPTAN1	GRCh38.p7	9:128577073	GGTCCCATGGGGTGT[C/T]CCTAGTTCTAGGGAG	6709
rs112594136	snp	A/T			intron-variant	SPTAN1	GRCh38.p7	9:128557611	TTTTTATTTGGGGAA[A/T]GAAAATTCCCCAAAT	6709
rs112626911	snp	A/G	0.0558544	0.157504	intron-variant	SPTAN1	GRCh38.p7	9:128571044	CCCAGAACTTTGGGA[A/G]GCCAAGGCTGAGGCA	6709
rs112671429	snp	C/T	0.5	0	intron-variant	SPTAN1	GRCh38.p7	9:128613760	TGTAATCCCAGCACT[C/T]TGGGAGGCCCAGACA	6709
rs112715602	snp	A/G	0.0539704	0.155153	intron-variant	SPTAN1	GRCh38.p7	9:128623507	GTTGCCCAGGCTGGG[A/G]TGCAGTGGCATGATC	6709
rs112770152	in-del	-/AAATAA	0.391954	0.205789	intron-variant	SPTAN1	GRCh38.p7	9:128601559	AAACCCCGGCTCTAC[-/AAATAA]AAATAAAAATGTTTT	6709
rs112771695	snp	A/G	0.00716266	0.059414	intron-variant	SPTAN1	GRCh38.p7	9:128627662	TCTGGAGCCGGGAGT[A/G]GGGGCATAGGTGGAG	6709
rs112855781	snp	A/G	0.00318978	0.0398085	intron-variant	SPTAN1	GRCh38.p7	9:128558100	GAGCCACCGCGCCCA[A/G]CTGTATATTAGAAAT	6709
rs112860044	snp	C/T	0.00279162	0.0372561	intron-variant	SPTAN1	GRCh38.p7	9:128565286	AGCCTGGTGACTGAG[C/T]GAGACTCCGTCTCAA	6709
rs112864065	snp	A/G			intron-variant	SPTAN1	GRCh38.p7	9:128562886	AGGAGAATGGCGTGA[A/G]CCCAGGAGGTGGAGC	6709
rs112867559	snp	C/T	0.00398564	0.0444627	intron-variant	SPTAN1	GRCh38.p7	9:128621025	TGTTCCTCTTTATTA[C/T]CCTCTTCCCCAGCTA	6709
rs112871782	snp	A/G	0.5	0	upstream-variant-2KB	SPTAN1	GRCh38.p7	9:128550621	CCCAGTTCACTATGG[A/G]GCCAGGGTGATTTAA	6709
rs112908635	in-del	-/G	0.0391387	0.134304	intron-variant	SPTAN1	GRCh38.p7	9:128623177	CTCCCACCTGAGCTT[-/G]CCCTAGCTAGCTGGG	6709
rs112945186	snp	A/C			splice-acceptor-variant	SPTAN1	GRCh38.p7	9:128607602	GGGGTGCTGGTTTCC[A/C]GGGACCTCATGTCTT	6709
rs112955915	snp	C/T	0.00564398	0.0528217	SPTAN1	9	allele_origin=T(germline)/C(germline)	9:128627469	TGCCCAGCACGCCAA[C/T]GCCTTCCACCAGTGG	6709
rs112985040	snp	A/G	0.00716266	0.059414	intron-variant	SPTAN1	GRCh38.p7	9:128597191	AAAAAAAATTTTTCT[A/G]TAGAGATAGGGGTCT	6709
rs113030949	snp	A/G	0.5	0	intron-variant	SPTAN1	GRCh38.p7	9:128603255	ATCATTAGTCTTTTA[A/G]GTATTTTTCTGTCCA	6709
rs113036663	snp	C/T	0.00438332	0.0466095	intron-variant	SPTAN1	GRCh38.p7	9:128628881	TCTGCTGGTCTTGCT[C/T]TTGTCTCCGTGAGGT	6709
rs113037526	in-del	-/A	0.371987	0.218218	intron-variant	SPTAN1	GRCh38.p7	9:128572330	TTCCACATGTTTATG[-/A]AGTGCACCTGCCTCC	6709
rs113106242	snp	C/T	0.00199481	0.0315187	intron-variant	SPTAN1	GRCh38.p7	9:128557148	AACCAAATGACCAAA[C/T]GACCCGTTCATCCTG	6709
rs113115179	snp	C/T	0.000399281	0.0141238	intron-variant	SPTAN1	GRCh38.p7	9:128566014	TTTGGCGTTAATCTG[C/T]ATCTGTTTCCTTCTG	6709
rs113157213	snp	A/G	5.37168e-05	0.00518223	synonymous-codon	SPTAN1	GRCh38.p7	9:128598426	CAATGAGTCACGGTT[A/G]AAGGACATTAACAAG	6709
rs113164547	snp	A/G	0.0410537	0.137264	intron-variant	SPTAN1	GRCh38.p7	9:128599355	GTCCAGGCTGGTCTC[A/G]AACTCCCAACCTCAG	6709
rs113166644	snp	A/G	0.5	0	intron-variant	SPTAN1	GRCh38.p7	9:128585495	AGTCTTTATGATACT[A/G]TCACTAATGCCAACT	6709
rs113188774	snp	C/T	0.5	0	intron-variant	SPTAN1	GRCh38.p7	9:128573105	TGTTAGTGTTTAAAC[C/T]GCTTTGTTTGTTTTA	6709
rs113208670	snp	A/G	0.0150606	0.0854603	intron-variant	SPTAN1	GRCh38.p7	9:128600373	ATGCTGCAGCAGGGA[A/G]CACTGTTGTTGGCAG	6709
rs113283272	snp	C/T	0.369958	0.21934	intron-variant	SPTAN1	GRCh38.p7	9:128560495	AAGGGATTCTCCAGC[C/T]CCAGCCTCCTGAGTA	6709
rs113308469	snp	A/G	0.5	0	intron-variant	SPTAN1	GRCh38.p7	9:128561033	AAAAAAAAAAAAAAA[A/G]AAGAAGTGAAAGGAA	6709
rs113312491	snp	C/G	0.0554779	0.157039	intron-variant	SPTAN1	GRCh38.p7	9:128574028	AAAGTGCTGGAATTA[C/G]AGGCATGAGCCGCTG	6709
rs113357847	snp	C/G/T	0.0145263	0.0839781	SPTAN1	9	allele_origin=T(germline)/C(germline)	9:128578256	ACAAGGTAATGGTAT[C/G/T]TCTAGAATCTTCCAG	6709
rs113364905	snp	A/G	0.5	0	intron-variant	SPTAN1	GRCh38.p7	9:128566650	CTGGGTTTATCTGAT[A/G]ATTATTTCTTTCCTT	6709
rs113429748	in-del	-/G	0	0	intron-variant	SPTAN1	GRCh38.p7	9:128584199	TCCTCTCAGGAATGG[-/G]AAAAAAGACCTTATC	6709
rs113498810	snp	C/G	0.0418186	0.138422	intron-variant	SPTAN1	GRCh38.p7	9:128592461	TGTATTTTTAGTAGA[C/G]ATGGGGTTTCACTGT	6709
rs113605698	snp	C/G	0.00318978	0.0398085	intron-variant	SPTAN1	GRCh38.p7	9:128624820	GGGCGCCACCCAGCT[C/G]CTGGGTGAGGGAAAA	6709
rs113649663	snp	C/T	0.0298908	0.118541	intron-variant	SPTAN1	GRCh38.p7	9:128586886	GCAGTGGCATGATCT[C/T]GGATAACTGCAACCT	6709
rs113830339	snp	C/T	0.5	0	intron-variant	SPTAN1	GRCh38.p7	9:128620876	ATAAGTCACTGTTGA[C/T]GGATGACAAAGGGTT	6709
rs113887407	snp	A/T	0.0410537	0.137264	intron-variant	SPTAN1	GRCh38.p7	9:128597957	CCCGGCCTGTTTTGT[A/T]TTGTTTTTGAGATGG	6709
rs113888454	snp	A/G	0.5	0	intron-variant	SPTAN1	GRCh38.p7	9:128631599	GGGAGGCCAAGACAG[A/G]CAGATCACTTGAGCC	6709
rs113912557	snp	C/T	0.0138799	0.0821421	utr-variant-3-prime, downstream-variant-500B	SPTAN1, WDR34	GRCh38.p7	9:128633482	GGTGCTTCACTAACC[C/T]GCTTCCGGTCCAGTC	6709
rs113944410	snp	A/G	0.5	0	intron-variant	SPTAN1	GRCh38.p7	9:128562073	ATTCAGAAAGACTTC[A/G]TAGAGGACGAGGCAT	6709
rs113961410	snp	A/T	0.5	0	intron-variant	SPTAN1	GRCh38.p7	9:128604245	TAGCATCTCCTTCAA[A/T]CAAAGTCATTTTCCC	6709
rs114019948	snp	A/C	0.0123036	0.0774623	intron-variant, upstream-variant-2KB	SPTAN1	GRCh38.p7	9:128554586	CTACACTAAGAATGG[A/C]CAAGTGTGTTCAAGG	6709
rs114061062	snp	A/G/T	0.00874735	0.0655527	intron-variant	SPTAN1	GRCh38.p7	9:128614453	AAAAATTAGCAGGGC[A/G/T]TGGCATGTGCCTATA	6709
rs114097313	snp	A/G	0.0441095	0.141807	intron-variant	SPTAN1	GRCh38.p7	9:128602542	TACTCAAAGGGTTGT[A/G]AGCATTATAACCTAG	6709
rs114106997	snp	G/T	0.0123036	0.0774623	intron-variant	SPTAN1	GRCh38.p7	9:128590288	CAGCATTGCCCAGTA[G/T]AACTTTCTGTGATGG	6709
rs114198206	snp	C/T	0.0441095	0.141807	intron-variant	SPTAN1	GRCh38.p7	9:128603902	TTGCCGCCTGCAGTG[C/T]GAGGTCCTGTGGCGT	6709
rs114209374	snp	C/T	0.0368353	0.130617	intron-variant	SPTAN1	GRCh38.p7	9:128617162	GAGGATCACTTGAAC[C/T]GGAGTGGCGGAGGTT	6709
rs114244970	snp	A/G	0.0349115	0.127424	intron-variant	SPTAN1	GRCh38.p7	9:128628561	GGGCTGGGCTGTCCC[A/G]CCCAGTCCCGGCAGG	6709
rs114246604	snp	C/G	0.0119091	0.0762411	intron-variant	SPTAN1	GRCh38.p7	9:128596851	ATAGGCTACCACATC[C/G]ATTATTATAATTGAA	6709
rs114297852	snp	G/T	0.0240643	0.107019	intron-variant	SPTAN1	GRCh38.p7	9:128564940	GTCACGGGTGAGAGA[G/T]AATACCAGGCAGGCA	6709
rs114523959	snp	C/T	0.00517822	0.0506191	intron-variant	SPTAN1	GRCh38.p7	9:128594723	AGGCATGAGCTTCTG[C/T]GCCTGGCCAGAGTCT	6709
rs114576138	snp	A/G	0.0144649	0.0838046	intron-variant	SPTAN1	GRCh38.p7	9:128628060	CCCAGGGCGGGCTGC[A/G]CTTCCCCTCCCACCC	6709
rs114602198	snp	A/C	0.0279526	0.114869	intron-variant	SPTAN1	GRCh38.p7	9:128614609	AAAAAACAAAAAAAA[A/C]ACACAAAAATTAATT	6709
rs114711747	snp	A/G	0.0119091	0.0762411	intron-variant	SPTAN1	GRCh38.p7	9:128580579	AGTTGACATTTCTTA[A/G]TGGAGAGTCCCTACT	6709
rs114715558	snp	A/G	0.00517822	0.0506191	intron-variant	SPTAN1	GRCh38.p7	9:128590903	GCACATGTGACTGGT[A/G]GCTACAGTGTTAGCA	6709
rs114745823	snp	A/G	0.00243501	0.0348077	SPTAN1	9	allele_origin=G(germline)/A(germline)	9:128612222	CAACACAGGGATCAA[A/G]GACTTTGACTTCTGG	6709
rs114880033	snp	C/T	0.0448719	0.142907	intron-variant	SPTAN1	GRCh38.p7	9:128560373	ACAGGTGTAAGCCAC[C/T]GTGCCCGCCTTTTTT	6709
rs114894578	snp	C/T	0.0441095	0.141807	intron-variant	SPTAN1	GRCh38.p7	9:128601460	GGCTAGGTGTTGTGG[C/T]TCACACCTGTAATCC	6709
rs114929460	snp	C/G	0.0391387	0.134304	upstream-variant-2KB	SPTAN1	GRCh38.p7	9:128552349	TTCCCCATCCTCCCG[C/G]GGCCCGCCCCTCGCT	6709
rs114942193	snp	A/G	0.0495547	0.149404	intron-variant	SPTAN1	GRCh38.p7	9:128578864	AAAAAACCTTCTGAG[A/G]GGTTTTAATGTGCTA	6709
rs114952624	snp	A/G	0.0123036	0.0774623	intron-variant	SPTAN1	GRCh38.p7	9:128582035	TTTCACAAGGATGAC[A/G]TGCTATCTCGTTGAA	6709
rs115077872	snp	C/T	0.067446	0.170804	intron-variant	SPTAN1	GRCh38.p7	9:128594918	ACTGCAACTCCTCCT[C/T]CCAGGTTCAAGCAGT	6709
rs115115952	snp	C/T	0.0670745	0.170406	intron-variant	SPTAN1	GRCh38.p7	9:128597441	AGGTAGGAGGATTGC[C/T]TGAGCCTGGGAGGTA	6709
rs115167110	snp	G/T	0.0150606	0.0854603	intron-variant	SPTAN1	GRCh38.p7	9:128590436	AAGCCGGGCATGGTG[G/T]CTCACGCCTGTAGTC	6709
rs115220884	snp	C/T	0.0150606	0.0854603	intron-variant	SPTAN1	GRCh38.p7	9:128601704	AATATGAAGAAAGCA[C/T]GAAAAGCTAAAAACA	6709
rs115221736	snp	C/T	0.00517822	0.0506191	intron-variant	SPTAN1	GRCh38.p7	9:128603754	CAGCACATTCATGGC[C/T]GCTGGGTAGCTTGGT	6709
rs115374283	snp	A/G	0.0448719	0.142907	intron-variant	SPTAN1	GRCh38.p7	9:128616732	AGATCGCACCACTGT[A/G]CTCCAGAGCAAGACT	6709
rs115428827	snp	C/T	0.00332252	0.0406229	SPTAN1	9	allele_origin=T(germline)/C(germline)	9:128582753	CCGGGCCCAGCTAGC[C/T]GATTCTTTCCATCTG	6709
rs115467682	snp	A/G	0.0360663	0.129354	intron-variant	SPTAN1	GRCh38.p7	9:128579076	AACTGAATAGATAGA[A/G]TGATTTATCTAGTAC	6709
rs115487948	snp	A/T	0.00199481	0.0315187	intron-variant	SPTAN1	GRCh38.p7	9:128615927	GTTGAGTGGTGAGGC[A/T]GGAAACCCTGCTGGA	6709
rs115656852	snp	C/T	0.0103295	0.0711199	intron-variant	SPTAN1	GRCh38.p7	9:128601640	GGTGAGTTTGACAAG[C/T]AAATAAAAAACAAAA	6709
rs115673747	snp	A/C	0.0162398	0.0886349	intron-variant, upstream-variant-2KB	SPTAN1	GRCh38.p7	9:128554453	TATGTCTTTTGGTTC[A/C]CTGGGTTAGAATTTT	6709
rs115744308	snp	A/G	0.0444908	0.142359	intron-variant	SPTAN1	GRCh38.p7	9:128596755	AGAGGGCAGTGGATG[A/G]TCATAGCTCACTGTA	6709
rs115750607	snp	A/G	0.00478085	0.0486577	intron-variant	SPTAN1	GRCh38.p7	9:128601338	TAACTGGTTGCCTGT[A/G]TCTCAGTTCTAGCAT	6709
rs115815276	snp	A/G	0.00276741	0.0370951	SPTAN1	9	allele_origin=G(germline)/A(germline)	9:128576817	TCTCTTCTCTTCCTT[A/G]TTTAGGAGCAGCACC	6709
rs115994415	snp	A/G	0.0310518	0.120672	intron-variant	SPTAN1	GRCh38.p7	9:128566118	GCGGAGCGCAGTGGT[A/G]CAATGATGGCTCACT	6709
rs116056440	snp	A/G	0.0310518	0.120672	intron-variant	SPTAN1	GRCh38.p7	9:128616188	CGAAAATGTCAGTCT[A/G]CTGATTCCAGTTGAT	6709
rs116114254	snp	C/T	0.00232678	0.0340291	intron-variant	SPTAN1	GRCh38.p7	9:128633005	TTTGGAAAACTAAAG[C/T]CAAATTTGTGGCAGA	6709
rs116463532	snp	A/G	0.0142736	0.0832652	intron-variant	SPTAN1	GRCh38.p7	9:128629579	GATTCGTCCCTGCAC[A/G]TAACCCTAACTCGTT	6709
rs116465900	snp	C/T	0.00240214	0.0345731	intron-variant	SPTAN1	GRCh38.p7	9:128577541	TCTTAACCAGTATCA[C/T]TTGGCTTCTTTTTTG	6709
rs116512692	snp	C/G	0.0134861	0.0810011	intron-variant	SPTAN1	GRCh38.p7	9:128583518	AACTGAATTGGGCCT[C/G]ATTGCTGAAAATCAA	6709
rs116561220	snp	A/C	0.0528381	0.153711	intron-variant	SPTAN1	GRCh38.p7	9:128626880	AGTGCAGTGGTGCTA[A/C]CATGGCTCCCTGTAG	6709
rs116617001	snp	A/G	0.0349115	0.127424	intron-variant	SPTAN1	GRCh38.p7	9:128563260	ACCTGTACAAAAAAT[A/G]TAAAAATTATCCAGG	6709
rs116699308	snp	A/G	0.00199481	0.0315187	intron-variant	SPTAN1	GRCh38.p7	9:128564608	AAATAAAAATCTGGT[A/G]TACAAATATTAGGTT	6709
rs116702176	snp	A/G	0.0221141	0.102801	intron-variant	SPTAN1	GRCh38.p7	9:128615155	TCTTTGAAGTGACAG[A/G]CTCACTTTATTTATT	6709
rs116735191	snp	C/T	0.0554779	0.157039	intron-variant	SPTAN1	GRCh38.p7	9:128580436	ATAAATAATGATTTA[C/T]ATGATTTATATGTTT	6709
rs116763351	snp	C/T	0.00102376	0.0226016	intron-variant	SPTAN1	GRCh38.p7	9:128630425	CCTTCACCCAGCCAC[C/T]CCCCAGGGTACCCCT	6709
rs116778543	snp	A/C	0.00282198	0.037457	SPTAN1	9	allele_origin=A(germline)/C(germline)	9:128626660	GGCCCTGGAGGAGAC[A/C]TGGAGGAACCTACAG	6709
rs116789302	snp	C/T	0.0103295	0.0711199	intron-variant	SPTAN1	GRCh38.p7	9:128572977	TCCTTTCAAGTAAAA[C/T]ATCCACACTTGTTTC	6709
rs116798421	snp	A/G	0.0162398	0.0886349	intron-variant, upstream-variant-2KB	SPTAN1	GRCh38.p7	9:128553962	CTTGGAAATAGCAGG[A/G]GGAACACTCAGCTAT	6709
rs116802004	snp	G/T	0.0678174	0.1712	intron-variant	SPTAN1	GRCh38.p7	9:128601454	TCTTTTGGCTAGGTG[G/T]TGTGGCTCACACCTG	6709
rs116909110	snp	C/T	0.0345262	0.126772	intron-variant	SPTAN1	GRCh38.p7	9:128592266	AAGAATGGGAGGTTT[C/T]GGTTTGTGTTCTTTT	6709
rs116916008	snp	A/G	0.0267878	0.112589	intron-variant	SPTAN1	GRCh38.p7	9:128626838	CTTTTTGTGTTCTTG[A/G]GGCAGGGTCTCTGTC	6709
rs116982822	snp	A/G	0.00914312	0.0669923	intron-variant	SPTAN1	GRCh38.p7	9:128622090	ATGTAGCTAAAATCC[A/G]CTTCACTGGAGAGCT	6709
rs116997688	snp	A/G	0.00636936	0.0560724	intron-variant	SPTAN1	GRCh38.p7	9:128568074	GCCAAAACTTTTTTT[A/G]TAAAAAGGGAAAGCC	6709
rs117001948	snp	A/G	0.0345262	0.126772	intron-variant	SPTAN1	GRCh38.p7	9:128614637	ATTAGCCAAACGTTG[A/G]GGTATGCACCTATAG	6709
rs117190550	snp	G/T	0.0356815	0.128715	intron-variant	SPTAN1	GRCh38.p7	9:128620924	CCAAAGACTGTCCCT[G/T]CTGAAGCCTGTCCCA	6709
rs117192752	snp	A/G	0.00199481	0.0315187	intron-variant	SPTAN1	GRCh38.p7	9:128587101	CCTGGGATTACAGGC[A/G]TGAGGCACCGCGCTC	6709
rs117336504	snp	A/G	0.000399281	0.0141238	intron-variant	SPTAN1	GRCh38.p7	9:128619978	CCTGATTGTCATCCA[A/G]CCTGGACATCTCTGT	6709
rs117373119	snp	C/T	0.0295035	0.117819	intron-variant	SPTAN1	GRCh38.p7	9:128561995	ACAATAATTTCATGG[C/T]AGAATGTGGCAGTGT	6709
rs117389491	snp	C/T	0.000399281	0.0141238	intron-variant	SPTAN1	GRCh38.p7	9:128587100	TCCTGGGATTACAGG[C/T]GTGAGGCACCGCGCT	6709
rs117391729	snp	A/G			intron-variant	SPTAN1	GRCh38.p7	9:128571291	CAAGACTGGGAAAAA[A/G]AAAAAAAAAAAGGCC	6709
rs117436936	snp	A/G	0.00136633	0.0261017	SPTAN1	9	allele_origin=G(germline)/A(germline)	9:128577290	TGGGTTTTACAAGCA[A/G]CTGATTCTGTAAATA	6709
rs117576726	snp	C/T	0.00993419	0.0697739	intron-variant	SPTAN1	GRCh38.p7	9:128607241	ATTCCTGAGCTCAAG[C/T]GATCCTCCTGCCTCA	6709
rs117614529	snp	A/G	0.000576944	0.0169747	SPTAN1	9	allele_origin=G(germline)/A(germline)	9:128605163	CGAGAGGGACCTTGC[A/G]GCTCTCGGTGACAAG	6709
rs117630545	snp	G/T	0.030665	0.119967	intron-variant	SPTAN1	GRCh38.p7	9:128613105	GATTCTTTCCTAGGG[G/T]GGTTTCCTTGAACTA	6709
rs117664291	snp	A/G	0.00557542	0.0525036	intron-variant	SPTAN1	GRCh38.p7	9:128600229	CTTTAGTCATTTCTG[A/G]ACTTGTTTGGGCTGG	6709
rs117714557	snp	G/T	0.0345262	0.126772	intron-variant	SPTAN1	GRCh38.p7	9:128602191	CTCCTGCCCTCCTGT[G/T]TTTTTTTTTGTTTTT	6709
rs117767685	snp	A/G	0.0345262	0.126772	intron-variant, upstream-variant-2KB	SPTAN1	GRCh38.p7	9:128553874	TGCGTCGTCATAGCA[A/G]TTGGCCTTAAGTAAA	6709
rs117770059	snp	A/G	0.0275645	0.114116	intron-variant	SPTAN1	GRCh38.p7	9:128597454	GCTTGAGCCTGGGAG[A/G]TAGAGACTGCAGTGA	6709
rs117848582	snp	C/T	0.0544748	0.155788	intron-variant	SPTAN1	GRCh38.p7	9:128626971	AAGCACGTGCCACCA[C/T]GCCTGGCTAATTATT	6709
rs117859036	snp	C/T	0.0345262	0.126772	intron-variant	SPTAN1	GRCh38.p7	9:128605579	CAGGGTACAATGGCT[C/T]ACACCTATAATCCAA	6709
rs117940811	snp	A/G	0.0345262	0.126772	intron-variant, upstream-variant-2KB	SPTAN1	GRCh38.p7	9:128554338	GGCAGTGTGTTTTGT[A/G]GTCATCTAATAATTG	6709
rs117975373	snp	A/C/T	0.0217436	0.10212	intron-variant	SPTAN1	GRCh38.p7	9:128589260	CTGTATAACTTGGAC[A/C/T]TGTTGGTTCTTTTTT	6709
rs117977733	snp	C/G	0.00358779	0.0422022	intron-variant	SPTAN1	GRCh38.p7	9:128579859	TATGTGAGAAACTTT[C/G]CTTTCTCTGCAGAGG	6709
rs118026701	snp	C/T	0.030665	0.119967	intron-variant	SPTAN1	GRCh38.p7	9:128598245	GAGCCACCATGCCCC[C/T]AGCCATAGCTTATTT	6709
rs118083072	snp	C/T	0.000399281	0.0141238	intron-variant	SPTAN1	GRCh38.p7	9:128593979	GAACAGTACAGTGTG[C/T]GCATATCTCTCAGGC	6709
rs118130569	snp	A/G	0.0225045	0.103662	intron-variant	SPTAN1	GRCh38.p7	9:128556341	ATCCCAAAATAAAAA[A/G]TATAAACATTGGAAA	6709
rs118148397	snp	A/C	0.00755907	0.0610114	intron-variant	SPTAN1	GRCh38.p7	9:128583406	TTTGGCGTTAGGGAT[A/C]ATTTCCTGTGTAGGA	6709
rs118162559	snp	C/G	0.00914312	0.0669923	intron-variant	SPTAN1	GRCh38.p7	9:128617483	TTCTTGGTCCCTACT[C/G]ATTTGGGAAGTAGAG	6709
rs137878312	snp	C/T	0.000399281	0.0141238	intron-variant	SPTAN1	GRCh38.p7	9:128576210	TCATATTTTTTAAAA[C/T]ACCAAAATGTGGTTG	6709
rs137913528	snp	A/C/T	0.000379465	0.0137701	intron-variant	SPTAN1	GRCh38.p7	9:128632556	CTGCTGAGCCGCCCT[A/C/T]GGCTTTGTGCTGCAG	6709
rs137947812	snp	A/G	0.000692886	0.0186001	synonymous-codon	SPTAN1	GRCh38.p7	9:128579657	AATTGATGCCCATGA[A/G]GACAGCTTCAAATCT	6709
rs137960444	snp	C/T	0.000798403	0.0199641	intron-variant	SPTAN1	GRCh38.p7	9:128596168	TTCCAGGTTCATCCT[C/T]TTTGTAGCACATACC	6709
rs137986838	snp	C/G	0.029116	0.117091	intron-variant	SPTAN1	GRCh38.p7	9:128568420	AAAACTGTTGGTATG[C/G]TTCTGTATTTCTAGA	6709
rs138014028	in-del	-/AAGTC	0.0126979	0.078662	intron-variant	SPTAN1	GRCh38.p7	9:128600210	CTGAATATTCAGCTT[-/AAGTC]TTTAGTCATTTCTGG	6709
rs138024180	snp	A/G	0.00557542	0.0525036	intron-variant	SPTAN1	GRCh38.p7	9:128606068	ACTACTGAATGCCAT[A/G]TTGTTAAAAATAAGT	6709
rs138030661	snp	C/T	0.00167926	0.0289277	intron-variant	SPTAN1	GRCh38.p7	9:128582590	CATGCTCCTCCTTTT[C/T]GGTACATGAATGTCT	6709
rs138036000	snp	A/T	9.89152e-05	0.00703192	intron-variant	SPTAN1	GRCh38.p7	9:128609021	ACCAGCCCTGAGAGG[A/T]TGCATCCCCTCATAC	6709
rs138038082	snp	A/G	0.000399281	0.0141238	intron-variant	SPTAN1	GRCh38.p7	9:128569551	AAAACAAACCTCTTG[A/G]CAGTGAGGTGTGCAC	6709
rs138081523	snp	A/G	0.000399281	0.0141238	intron-variant	SPTAN1	GRCh38.p7	9:128573296	AACCCAAAGATGCTG[A/G]GAAGTGAATACGTTT	6709
rs138101005	snp	A/G	0.00107242	0.0231314	SPTAN1	9	allele_origin=G(germline)/A(germline)	9:128585797	TCACGAGCTGAACCA[A/G]AAGTGGGAGGCACTG	6709
rs138144532	snp	C/T	0.000399281	0.0141238	intron-variant	SPTAN1	GRCh38.p7	9:128587154	ACAGTGATGCAATCA[C/T]GACTCCCTACAGCTT	6709
rs138275607	snp	A/G	0.000181475	0.00952389	missense	SPTAN1	GRCh38.p7	9:128585940	TGGGCAGCACTGACT[A/G]TGGCAAGGACGAAGA	6709
rs138303805	snp	C/G	0.00023281	0.0107866	intron-variant	SPTAN1	GRCh38.p7	9:128615582	TCTTATGTTCAAGCA[C/G]ATAGCTGTGGGAGAC	6709
rs138305416	snp	C/G	3.29625e-05	0.00405958	synonymous-codon	SPTAN1	GRCh38.p7	9:128625897	CCGGCACGCCTCCCT[C/G]ATGAAGAGGTGGAGC	6709
rs138320965	snp	A/G	6.69905e-05	0.00578712	synonymous-codon	SPTAN1	GRCh38.p7	9:128624465	GTTCAACTGGAAGGC[A/G]GACGTGGTGGAGTCC	6709
rs138399852	snp	A/G	0.00358779	0.0422022	intron-variant	SPTAN1	GRCh38.p7	9:128572925	GCCAACAGTGGTGGA[A/G]GTGAATTGTGTGAGC	6709
rs138411842	snp	C/T	0.0383715	0.133092	intron-variant	SPTAN1	GRCh38.p7	9:128590661	TTGAGACCATCCTGG[C/T]CAACATGGTGAAACC	6709
rs138423655	snp	A/G	0.000399281	0.0141238	intron-variant	SPTAN1	GRCh38.p7	9:128628757	GACCCATCCAGCCGG[A/G]CCACACATTCTGATG	6709
rs138442944	snp	G/T	0.00478085	0.0486577	intron-variant	SPTAN1	GRCh38.p7	9:128595301	TTTTAGTACAACCGG[G/T]ATTTTGCCATGTTGG	6709
rs138463763	snp	A/G	0.0162398	0.0886349	intron-variant	SPTAN1	GRCh38.p7	9:128556923	GCTAATCAATTCTTT[A/G]GTGGTTTGTTCTTAG	6709
rs138499933	in-del	-/CTTC	0.0150606	0.0854603	intron-variant	SPTAN1	GRCh38.p7	9:128577576	AGGAATAGCAGAGTT[-/CTTC]AAGGGTCTGTTCTGT	6709
rs138576972	snp	C/T	0.00517822	0.0506191	intron-variant	SPTAN1	GRCh38.p7	9:128613812	AGTTCGAGACCACTC[C/T]GGCCAACGTGGTGAG	6709
rs138609094	snp	A/G	0.00161452	0.0283664	SPTAN1	9	allele_origin=G(germline)/A(germline)	9:128576945	GGCAGCAGAAGTTCA[A/G]CGCTTTAACAGGTGT	6709
rs138634476	snp	C/T	0.000495704	0.0157355	SPTAN1, WDR34	9	allele_origin=T(germline)/C(germline)	9:128633259	CCACATGAAGCCCTA[C/T]GTGGACGGCAAGGGC	6709
rs138697290	snp	A/G	0.00318978	0.0398085	intron-variant	SPTAN1	GRCh38.p7	9:128602091	CTTATTGGAGACAGT[A/G]GGTCCACCTTCTGAC	6709
rs138730117	snp	A/G	0.0352966	0.128072	intron-variant	SPTAN1	GRCh38.p7	9:128605763	TTGGTAGGCCAAGGC[A/G]GGCAGATCACCTGAG	6709
rs138827421	snp	C/T	1.65211e-05	0.00287407	missense	SPTAN1	GRCh38.p7	9:128605458	TCCCACGACCTGCAG[C/T]GCTTCCTTAGCGATT	6709
rs138961673	snp	C/T	0.00279162	0.0372561	intron-variant	SPTAN1	GRCh38.p7	9:128624165	TGTGAAGCCTTTGAC[C/T]GCATTGCTCTTACAA	6709
rs138965195	snp	C/T	0.00399342	0.0445058	intron-variant	SPTAN1	GRCh38.p7	9:128632985	AGGTGGGTGAAGAGG[C/T]GTCCTTTGGAAAACT	6709
rs138968543	snp	G/T	0.000399281	0.0141238	intron-variant	SPTAN1	GRCh38.p7	9:128628508	AATGCACCCGTTATG[G/T]GATAGACAGGACGTG	6709
rs138985089	snp	C/T	0.00033145	0.0128691	synonymous-codon	SPTAN1	GRCh38.p7	9:128632880	GAACGTCAAGTCCAG[C/T]GAGGAGATTGAGAGC	6709
rs138991306	snp	A/G			intron-variant	SPTAN1	GRCh38.p7	9:128590242	TTTAAACCTAAACCA[A/G]CTTGTGGTCTAACTT	6709
rs139015346	snp	A/C/T	0.0845547	0.19091	intron-variant	SPTAN1	GRCh38.p7	9:128589319	TTTGAGACAGAGTCT[A/C/T]GCTCTGTCACCCAGG	6709
rs139049596	snp	C/T	0.00169339	0.0290487	SPTAN1	9	allele_origin=T(germline)/C(germline)	9:128583066	AAAGAACCCCCTTCT[C/T]TTATTCACAGGATCC	6709
rs139070536	snp	C/T	1.65272e-05	0.0028746	missense, downstream-variant-500B	SPTAN1, WDR34	GRCh38.p7	9:128633291	GCGAGCTCCCCACCG[C/T]GTTCGACTACGTGGA	6709
rs139091539	snp	A/G	0.000798403	0.0199641	intron-variant	SPTAN1	GRCh38.p7	9:128586967	GGATTACAGGCGCCC[A/G]CCACCACGCCCAGCT	6709
rs139113273	snp	A/C	3.30393e-05	0.0040643	missense	SPTAN1	GRCh38.p7	9:128608909	GCAGGCCTTTGCCGA[A/C]CAGCTCATCGCTGCC	6709
rs139117026	snp	A/T	0.00119737	0.0244387	intron-variant	SPTAN1	GRCh38.p7	9:128617365	ATAATTTGATAGGGC[A/T]CCTCAGGGCAGCACT	6709
rs139179012	snp	C/T	0.000399281	0.0141238	intron-variant	SPTAN1	GRCh38.p7	9:128599164	TTTTGAGACGGAGTC[C/T]CACTCTGTCAACCAG	6709
rs139237046	snp	A/T	0.00199481	0.0315187	intron-variant	SPTAN1	GRCh38.p7	9:128621454	GTAAAGTTATTCTGC[A/T]GTGCTTATTTTTTCT	6709
rs139262591	snp	A/C	0.0345262	0.126772	intron-variant	SPTAN1	GRCh38.p7	9:128573815	CTGAAGCACAGTGGC[A/C]CAATCATGGCTCACT	6709
rs139281148	snp	A/G	0.000399281	0.0141238	intron-variant	SPTAN1	GRCh38.p7	9:128565939	ACTTTAGGAAATTGA[A/G]GCATGGAGAGGGAAG	6709
rs139321348	snp	A/C	0.00917046	0.0670905	intron-variant	SPTAN1	GRCh38.p7	9:128630526	CTAGGGCTCTTCACT[A/C]TCTCTCTCTCTTTTC	6709
rs139355278	snp	G/T	0.00159617	0.0282053	intron-variant	SPTAN1	GRCh38.p7	9:128616777	TAAAAAATAAAAATA[G/T]AAAAATTAGCTGGGC	6709
rs139447855	snp	C/T	0.00874735	0.0655527	intron-variant	SPTAN1	GRCh38.p7	9:128629322	GTCCTCCCACTGCAC[C/T]GGCACCCAGCCTCCT	6709
rs139449739	snp	A/G	0.00716266	0.059414	intron-variant	SPTAN1	GRCh38.p7	9:128555595	ATCAGAAGTATTAGT[A/G]AATTTACTTGAAAAT	6709
rs139452213	snp	A/G	0.00119737	0.0244387	intron-variant	SPTAN1	GRCh38.p7	9:128562369	GCTTCCCAAAGTGCT[A/G]GGATTACAGGCGTGA	6709
rs139457682	snp	C/T	0.000798403	0.0199641	intron-variant	SPTAN1	GRCh38.p7	9:128622010	ATGAGTAAGATTTCT[C/T]ATCACAGAGGTTGCA	6709
rs139541887	snp	G/T	0.000399281	0.0141238	intron-variant	SPTAN1	GRCh38.p7	9:128599788	TTGCAGACAATCTTA[G/T]GAGTACAACATAAAA	6709
rs139598593	snp	C/T	0.00517822	0.0506191	intron-variant	SPTAN1	GRCh38.p7	9:128565384	ATAAAACATTTTGGA[C/T]TGTGGAAAAACAATA	6709
rs139645597	snp	A/G	0.00199481	0.0315187	intron-variant	SPTAN1	GRCh38.p7	9:128602888	TGATCCACCCACTTT[A/G]GTCCCCCAAAGTGCT	6709
rs139694176	snp	C/T	0.00159617	0.0282053	intron-variant	SPTAN1	GRCh38.p7	9:128606644	ATGCACCACCAAGCC[C/T]GGCTAATTTTGTATT	6709
rs139799727	snp	C/T	0.00491672	0.0493375	SPTAN1	9	allele_origin=T(germline)/C(germline)	9:128625810	CTTCCAGCAGGAAGG[C/T]ATTGCCAACATCACT	6709
rs139821848	snp	A/G	0.0150606	0.0854603	intron-variant	SPTAN1	GRCh38.p7	9:128596978	TAGCCTGGCCAACAT[A/G]GCAAAACCCCATCTC	6709
rs139844879	snp	A/G	0.00261814	0.0360862	intron-variant	SPTAN1	GRCh38.p7	9:128588763	TACTTAGATGACTCA[A/G]CGCGGACGTGTTTTT	6709
rs139867209	snp	A/G	0.000399281	0.0141238	intron-variant	SPTAN1	GRCh38.p7	9:128610440	AGGCGGTGGGAGAAC[A/G]TAACAAGGACATTTC	6709
rs139880239	snp	C/G	1.65479e-05	0.0028764	missense	SPTAN1	GRCh38.p7	9:128583131	GCTTTTGAGGCTGAG[C/G]TCTCAGCAAACCAGA	6709
rs139943747	snp	A/G	1.64754e-05	0.00287009	missense	SPTAN1	GRCh38.p7	9:128574808	TGATGGACTGGATCA[A/G]TGACAAGGCACGTTT	6709
rs139998823	snp	A/G	4.94271e-05	0.00497102	missense	SPTAN1	GRCh38.p7	9:128582707	AGCTGTTGAGCCGCC[A/G]CAATGCCCTTCACGA	6709
rs140035113	snp	A/G	0.0134861	0.0810011	intron-variant	SPTAN1	GRCh38.p7	9:128566346	CAAGTGTGCGCCACC[A/G]CACCCCCTGCTTGAA	6709
rs140055147	snp	C/T	0.00159617	0.0282053	intron-variant	SPTAN1	GRCh38.p7	9:128570235	CTTCAGTAATTAAGG[C/T]GGAAGGGAGGAGGAC	6709
rs140076136	snp	A/G	4.94458e-05	0.00497197	missense	SPTAN1	GRCh38.p7	9:128577380	GTGCTGAGGCTGACC[A/G]CCTGCAACAGTCCCA	6709
rs140117961	snp	C/T	0.00199481	0.0315187	intron-variant	SPTAN1	GRCh38.p7	9:128585513	ACTAATGCCAACTTG[C/T]GATATCTGCTTCTTA	6709
rs140128721	in-del	-/GG			intron-variant	SPTAN1	GRCh38.p7	9:128586111	ATCCATTTTTCACTT[-/GG]TTTTTTTTTTTTTTT	6709
rs140159000	snp	C/T	3.29533e-05	0.00405901	missense	SPTAN1	GRCh38.p7	9:128607970	AGCAGAAACTTGATA[C/T]TCTTGACCAGGAGCG	6709
rs140191388	snp	A/G	0.00109159	0.0233368	SPTAN1	9	allele_origin=G(germline)/A(germline)	9:128617742	AGCAGAACTGGCTGC[A/G]CATGAGCCGGCTATT	6709
rs140213586	snp	C/T	0.000399281	0.0141238	intron-variant	SPTAN1	GRCh38.p7	9:128613192	CTAGGTTTGACTGAC[C/T]GAGTGGAGAGAGTGT	6709
rs140227831	snp	C/T	0.00835141	0.0640778	intron-variant	SPTAN1	GRCh38.p7	9:128606819	TTGAGGTAAAAGCCA[C/T]GTAACATACAATTAA	6709
rs140241053	snp	C/T	0.000495098	0.0157259	SPTAN1	9	allele_origin=T(germline)/C(germline)	9:128632423	CCTAATTTCTGTTTT[C/T]CTTCCAGGAACACAA	6709
rs140253935	snp	C/T	0.00914312	0.0669923	intron-variant	SPTAN1	GRCh38.p7	9:128618552	GCAGTGGCACAATCT[C/T]GGCTCACTGCAAGCT	6709
rs140279996	snp	A/C/G	0.00245146	0.0349249	SPTAN1	9	allele_origin=G(germline)/A(germline)	9:128591521	TCAGGGTTTTGTGCC[A/C/G]GCTGCGTACGTGAAG	6709
rs140301253	snp	A/G	0.000399281	0.0141238	intron-variant	SPTAN1	GRCh38.p7	9:128582357	ACCAACCTTTGGGTG[A/G]AAACCTTGACCTATG	6709
rs140353002	snp	C/T	0.00148997	0.0272537	SPTAN1	9	allele_origin=T(germline)/C(germline)	9:128621199	TGAGACAGACTTCAC[C/T]GTCCACAAGGATCGC	6709
rs140418358	snp	C/T	0.000297039	0.0121832	synonymous-codon	SPTAN1	GRCh38.p7	9:128626528	GCGCGAGGCCCACGA[C/T]GCCTTCCGCTCCTCC	6709
rs140422066	snp	A/C	0.000798403	0.0199641	intron-variant	SPTAN1	GRCh38.p7	9:128623718	GCCTCAAATGATCTG[A/C]CCACCTCAGCCTCCC	6709
rs140439572	snp	A/G	0.000399281	0.0141238	intron-variant	SPTAN1	GRCh38.p7	9:128556607	CATTTCTGGATTTTG[A/G]TGCAATGCAGTATGA	6709
rs140456277	snp	A/G	0.0170251	0.090679	intron-variant	SPTAN1	GRCh38.p7	9:128608691	AACTCTACTCTAGTA[A/G]TGAATGAAATCAAGC	6709
rs140466374	snp	C/T	0.0337553	0.125452	intron-variant	SPTAN1	GRCh38.p7	9:128626295	CAGGCTGTGTGCGCC[C/T]CTGATTCCCAGGAAC	6709
rs140531706	snp	A/G	0.00279162	0.0372561	intron-variant	SPTAN1	GRCh38.p7	9:128629828	TTTGTCTGCAGGGTC[A/G]TGCTCTCATTCCCCC	6709
rs140536665	snp	A/G	0.0107246	0.0724382	intron-variant	SPTAN1	GRCh38.p7	9:128560368	GGATTACAGGTGTAA[A/G]CCACCGTGCCCGCCT	6709
rs140643168	snp	C/T	0.0399052	0.1355	intron-variant	SPTAN1	GRCh38.p7	9:128567401	GGTTCGAGTGATTCT[C/T]CAGCCTCAGCCTCCC	6709
rs140671384	snp	C/T	0.000399281	0.0141238	intron-variant	SPTAN1	GRCh38.p7	9:128631768	GGAGGTTGCAGTGAG[C/T]GTGATTGCGCCACTG	6709
rs140746652	snp	C/G	0.0345262	0.126772	intron-variant	SPTAN1	GRCh38.p7	9:128594686	ATCCACCCGCCTCAG[C/G]CTCCCAAAGTACTGG	6709
rs140796315	snp	A/G	3.29473e-05	0.00405864	missense	SPTAN1	GRCh38.p7	9:128594282	TACAGCAATGGATCA[A/G]TGAGAAGGAAGCCGC	6709
rs140799276	snp	A/C	0.000399281	0.0141238	intron-variant	SPTAN1	GRCh38.p7	9:128572460	GTTCCAGTACTGGGA[A/C]AGGCCTTGCCCTAGT	6709
rs140838494	snp	C/T	0.0345262	0.126772	intron-variant	SPTAN1	GRCh38.p7	9:128613731	TTTTAAGGCCAGGTG[C/T]AGTGGCTTACGGCTG	6709
rs140856932	snp	A/G	3.29484e-05	0.00405871	synonymous-codon	SPTAN1	GRCh38.p7	9:128630342	TATGGTGGAAGAGTC[A/G]GGGACCCTCGAATCC	6709
rs140911233	snp	A/G	0.000798403	0.0199641	intron-variant	SPTAN1	GRCh38.p7	9:128607335	TTTGAAGCTATCAAA[A/G]ACTTAATTGTAGCTA	6709
rs140917884	snp	C/T	0.000798403	0.0199641	intron-variant	SPTAN1	GRCh38.p7	9:128589952	GCTGTGACCTCACCC[C/T]ACAGGCTTTGTCTTC	6709
rs140922514	snp	C/T	0.000181325	0.00951996	intron-variant	SPTAN1	GRCh38.p7	9:128611864	TGGCCCACCAGCTCC[C/T]GGTGCCCAGGGAGGA	6709
rs140923686	in-del	-/T			intron-variant	SPTAN1	GRCh38.p7	9:128622316	TTTTTTTTTTTTTTT[-/T]GCGACGGAGTTTCGC	6709
rs140939957	snp	A/T	3.30639e-05	0.00406581	synonymous-codon	SPTAN1	GRCh38.p7	9:128584380	GGAAGCCCTCGTGGC[A/T]CGCTATGAGGCACTC	6709
rs140983075	snp	C/T	0.0410537	0.137264	intron-variant	SPTAN1	GRCh38.p7	9:128573988	TTGAACTCCTGACCT[C/T]GTGCTCTGCCCGCCT	6709
rs141121684	snp	C/T	0.0581099	0.160244	intron-variant	SPTAN1	GRCh38.p7	9:128600809	CTGGGACTACAGGCA[C/T]GTGCCACCATGCCTG	6709
rs141135038	snp	C/T	0.0337553	0.125452	intron-variant	SPTAN1	GRCh38.p7	9:128625599	TGCCGCAGTGATCTG[C/T]GGTCTGAAGGAGAGC	6709
rs141137621	snp	G/T	0.0225045	0.103662	intron-variant	SPTAN1	GRCh38.p7	9:128602190	CCTCCTGCCCTCCTG[G/T]TTTTTTTTTTGTTTT	6709
rs141161565	snp	C/T	0.00478085	0.0486577	intron-variant	SPTAN1	GRCh38.p7	9:128576469	TAACAGCCTCATGAA[C/T]ATCTGAAATACCAAA	6709
rs141200509	snp	C/T	0.00478085	0.0486577	intron-variant	SPTAN1	GRCh38.p7	9:128563587	AACTGGATAGAATTC[C/T]AATTTTACAATATGC	6709
rs141279297	snp	A/G	0.000399281	0.0141238	intron-variant	SPTAN1	GRCh38.p7	9:128604199	AATTTATTCAGCGAG[A/G]AAGGTTGGAAACAGG	6709
rs141354175	snp	G/T	0.000399281	0.0141238	intron-variant	SPTAN1	GRCh38.p7	9:128555877	GTTTCCTGTTGCATT[G/T]ACTTCTTCCACCACA	6709
rs141409593	snp	A/G	1.64811e-05	0.00287059	missense	SPTAN1	GRCh38.p7	9:128613396	GTGGAGGCCCTGCTG[A/G]CATCCGAAGATTATG	6709
rs141424626	snp	A/G	1.64727e-05	0.00286986	synonymous-codon	SPTAN1	GRCh38.p7	9:128581832	GGATAGTGTGGAAGC[A/G]CTTCTTAAGAAGCAC	6709
rs141473604	snp	G/T	0.000798403	0.0199641	intron-variant	SPTAN1	GRCh38.p7	9:128560873	GTACAAAAATTAGTC[G/T]CGTGTGGTGGCGGGT	6709
rs141474640	snp	C/T	3.3195e-05	0.00407387	synonymous-codon	SPTAN1	GRCh38.p7	9:128624351	CCATGAGGAGAACAT[C/T]TCTTCAAAGATGAAG	6709
rs141475745	snp	G/T	0.00034587	0.0131459	intron-variant	SPTAN1	GRCh38.p7	9:128627965	TTGTTTTCTTCCTTC[G/T]CTGGGCTTGTCATGT	6709
rs141483578	snp	A/G	1.64765e-05	0.00287019	missense	SPTAN1	GRCh38.p7	9:128615752	CAGAAGATCAAGAGC[A/G]TGGCGGCCTCCCGGC	6709
rs141502808	snp	A/G	0.00478085	0.0486577	intron-variant	SPTAN1	GRCh38.p7	9:128561478	ACCATCCTGGCTAAT[A/G]TGGTGAAACCCCATC	6709
rs141551809	snp	C/T	0.000798403	0.0199641	intron-variant	SPTAN1	GRCh38.p7	9:128586989	CGCCCAGCTAACTTT[C/T]TTTGTATTTTTAGGA	6709
rs141602301	snp	C/T	6.59044e-05	0.00574002	synonymous-codon	SPTAN1	GRCh38.p7	9:128625849	AGATCAGCTTCTCGC[C/T]GCCAAACACGTTCAG	6709
rs141694193	snp	C/T	0.0134861	0.0810011	intron-variant	SPTAN1	GRCh38.p7	9:128589874	GCCACCGCGCCTGGC[C/T]GACCTGTTGGTTCTT	6709
rs141696651	snp	A/C	0.000420901	0.0145008	missense	SPTAN1	GRCh38.p7	9:128598503	AGGCTGTGCAACAAC[A/C]GGTAGGTGTCTCCAT	6709
rs141754049	snp	A/C	0.000399281	0.0141238	intron-variant	SPTAN1	GRCh38.p7	9:128603701	TGACCTGTGACATAT[A/C]TCACTCTATTGGGTC	6709
rs141803274	snp	C/T	0.00159617	0.0282053	intron-variant	SPTAN1	GRCh38.p7	9:128602463	CTCACCTGATCCACC[C/T]GCCTTGGCCTCCCAA	6709
rs141837522	snp	C/G	0.00478085	0.0486577	intron-variant	SPTAN1	GRCh38.p7	9:128605789	CTGAGGTCAAGAGTT[C/G]AAGACCAGCCTGGCC	6709
rs141928816	snp	A/C	0.067446	0.170804	intron-variant	SPTAN1	GRCh38.p7	9:128595362	TGATCTGCCCACCTC[A/C]GCTTCCCAAGGTGCT	6709
rs141939928	snp	C/G	0.0213707	0.101413	intron-variant	SPTAN1	GRCh38.p7	9:128571484	CAGCTAGTTGGGAGG[C/G]TGAAGCAGGAGAATT	6709
rs141980692	snp	A/G	0.000746225	0.0193017	missense, downstream-variant-500B	SPTAN1, WDR34	GRCh38.p7	9:128633219	CACAGAACCTGACCC[A/G]GGAACAAGCCGACTA	6709
rs142003183	snp	C/T	0.0345262	0.126772	intron-variant	SPTAN1	GRCh38.p7	9:128585286	CACCTACCTCGGCCT[C/T]CCAAAGTGCTGGGAT	6709
rs142093503	snp	C/G	0.00119737	0.0244387	intron-variant	SPTAN1	GRCh38.p7	9:128628563	GCTGGGCTGTCCCGC[C/G]CAGTCCCGGCAGGGA	6709
rs142110449	snp	A/G	0.000464253	0.0152286	intron-variant	SPTAN1	GRCh38.p7	9:128588771	TGACTCAGCGCGGAC[A/G]TGTTTTTACCATGTT	6709
rs142114097	snp	C/T	0.0134861	0.0810011	intron-variant	SPTAN1	GRCh38.p7	9:128588468	AGGCACGCACCACCA[C/T]GCCTGTCTAGTTTTG	6709
rs142114177	snp	C/T	0.0345262	0.126772	intron-variant	SPTAN1	GRCh38.p7	9:128612796	CCAGGCGTGGTGGCA[C/T]GCTCCTGTAATCCCA	6709
rs142120579	snp	C/T	4.94303e-05	0.00497119	missense	SPTAN1	GRCh38.p7	9:128574702	GAGCTGCACCGCCAG[C/T]GGGAATTACTTTTGG	6709
rs142148896	snp	C/T	0.0023933	0.0345097	intron-variant	SPTAN1	GRCh38.p7	9:128629876	CCTCAGGAACCTTGC[C/T]GGGACACTCCAGGGT	6709
rs142153107	snp	C/G	0.0441095	0.141807	intron-variant	SPTAN1	GRCh38.p7	9:128562789	CTAGCACGGTGAAAC[C/G]CCATCTCTACTAAAA	6709
rs142154708	snp	A/G			intron-variant	SPTAN1	GRCh38.p7	9:128590426	TAACTCGATGAAGCC[A/G]GGCATGGTGGCTCAC	6709
rs142161809	snp	A/G	0.000153988	0.00877328	synonymous-codon	SPTAN1	GRCh38.p7	9:128611734	GCACCAGAAGCACCA[A/G]GCTTTTGAAGCAGAG	6709
rs142169147	snp	C/T	0.0670745	0.170406	intron-variant	SPTAN1	GRCh38.p7	9:128589649	GGCATGATCTCAGCT[C/T]ACTACAAGCTCCACC	6709
rs142210358	snp	A/G	0.000788134	0.0198355	downstream-variant-500B, missense	SPTAN1, WDR34	GRCh38.p7	9:128633856	CCCTGGGCATCGCCC[A/G]CAGCCAAGAGCTGAG	6709
rs142234188	snp	A/G	6.62526e-05	0.00575516	synonymous-codon	SPTAN1	GRCh38.p7	9:128617751	GGCTGCGCATGAGCC[A/G]GCTATTCAGGTAAGG	6709
rs142248213	snp	C/T	0.000399281	0.0141238	intron-variant	SPTAN1	GRCh38.p7	9:128566657	TATCTGATAATTATT[C/T]CTTTCCTTCAGAGAG	6709
rs142305088	snp	C/T	0.000165653	0.00909939	synonymous-codon	SPTAN1	GRCh38.p7	9:128604391	CCAGCTCTTGGGCAG[C/T]GCCCATGAAGTACAG	6709
rs142346263	in-del	-/C			intron-variant	SPTAN1	GRCh38.p7	9:128557799	TTAAATTAGAAATTT[-/C]TTTTTTTTTTTTTTT	6709
rs142349324	snp	C/T	0.000798403	0.0199641	intron-variant	SPTAN1	GRCh38.p7	9:128619322	ACGGAGTGGCACGAA[C/T]GGAGTACCACAGACA	6709
rs142405742	snp	C/T	1.64893e-05	0.0028713	synonymous-codon	SPTAN1	GRCh38.p7	9:128588848	GAGACTGGGAAGGAG[C/T]TGGTCTTGGCTCTCT	6709
rs142410041	snp	A/G	0.000153988	0.00877328	missense	SPTAN1	GRCh38.p7	9:128579673	GACAGCTTCAAATCT[A/G]CAGATGAATCTGGAC	6709
rs142465036	snp	C/T	0.00119737	0.0244387	intron-variant	SPTAN1	GRCh38.p7	9:128603682	CTTGTTCTTGTCAAC[C/T]GGGTGACCTGTGACA	6709
rs142486698	snp	A/C	0.000798403	0.0199641	intron-variant	SPTAN1	GRCh38.p7	9:128623417	TTTCTATCAAAAATA[A/C]TACTAATGAATATAT	6709
rs142498180	snp	A/G	6.63537e-05	0.00575955	missense	SPTAN1	GRCh38.p7	9:128624376	ATGAAGGGCCTGAAC[A/G]GGAAAGTGTCAGACC	6709
rs142535936	snp	A/G			intron-variant	SPTAN1	GRCh38.p7	9:128594994	TTTGTATTTTTAGTA[A/G]AGATGAGGTTTCACC	6709
rs142557287	snp	C/T	0.00517822	0.0506191	intron-variant, upstream-variant-2KB	SPTAN1	GRCh38.p7	9:128555054	AAAAAGTATATTCGG[C/T]ATTATTACTTTAACA	6709
rs142561856	snp	A/C	0.00557542	0.0525036	intron-variant	SPTAN1	GRCh38.p7	9:128571165	CGTGGTGGTGCACAC[A/C]TGTAGCCCCAGCTAC	6709
rs142566802	snp	C/T	0.0023933	0.0345097	intron-variant	SPTAN1	GRCh38.p7	9:128607363	CTAGAACTTGTTATT[C/T]TGGAGGGTGAAAAGA	6709
rs142570084	snp	C/T	0.000798403	0.0199641	intron-variant	SPTAN1	GRCh38.p7	9:128573355	TTGGAATAAACCTCA[C/T]TTGAGATGTACCACA	6709
rs142591751	snp	A/G	0.0345262	0.126772	intron-variant	SPTAN1	GRCh38.p7	9:128596816	CCACCTCAGCCACCC[A/G]AGTGGCTGGGACTAT	6709
rs142682344	snp	C/G	0.00391356	0.044062	SPTAN1	9	allele_origin=G(germline)/C(germline)	9:128598949	ATAAAACTGGTTTCT[C/G]TCTCTCCTTGTAGGA	6709
rs142695971	in-del	-/CT	0.0368353	0.130617	intron-variant	SPTAN1	GRCh38.p7	9:128568066	TGCACTCGGCCAAAA[-/CT]TTTTTTATAAAAAGG	6709
rs142702835	snp	A/C/G	0.0107347	0.0725747	intron-variant	SPTAN1	GRCh38.p7	9:128561789	ATCCTGGCCTTTGCA[A/C/G]CTTGCTTACTAAATT	6709
rs142777123	snp	C/T	0.000148742	0.00862258	SPTAN1, WDR34	9	allele_origin=T(germline)/C(germline)	9:128633265	GAAGCCCTACGTGGA[C/T]GGCAAGGGCCGCGAG	6709
rs142830725	snp	G/T	0.000708945	0.0188141	SPTAN1	9	allele_origin=G(germline)/T(germline)	9:128625152	TGGCCGAGACCTGTC[G/T]TCTGTGCAGACGCTC	6709
rs142896330	snp	C/T	0.0111196	0.0737302	intron-variant	SPTAN1	GRCh38.p7	9:128606429	AAGTATGGGCATACT[C/T]CCTCTCATCTCCTTG	6709
rs142922432	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	SPTAN1	GRCh38.p7	9:128553606	ACTAGAGTAAAATAT[A/G]TTTTAAATAAGCGCC	6709
rs142927505	snp	A/G	0.0349115	0.127424	intron-variant	SPTAN1	GRCh38.p7	9:128596528	TGATCCACCCGCCTC[A/G]GTCTCCCAAAGTGCT	6709
rs142928576	snp	C/T	0.00199481	0.0315187	intron-variant	SPTAN1	GRCh38.p7	9:128620514	CTGAGGTCAGGAGTC[C/T]GAGACCAACCTGGCC	6709
rs142964132	snp	A/G	0.000247392	0.0111191	SPTAN1	9	allele_origin=G(germline)/A(germline)	9:128617697	CCTAACCGGCGTGCA[A/G]AACCTGAGGAAGAAG	6709
rs142967011	snp	A/C	0.000438588	0.0148021	intron-variant	SPTAN1	GRCh38.p7	9:128583312	TTGAATTGTGACATG[A/C]ATGTTTGGGGAACTA	6709
rs142994022	snp	A/G	0.00597247	0.0543191	intron-variant	SPTAN1	GRCh38.p7	9:128571140	AAAAAAAATTTAAAA[A/G]TTAGTGGGGCGTGGT	6709
rs143004941	in-del	-/TC	0.00348735	0.0416114	intron-variant	SPTAN1	GRCh38.p7	9:128627126	CCAGAAGTTTCCATT[-/TC]TGACAGTCCAGCAAC	6709
rs143006800	snp	A/T	0.00119737	0.0244387	intron-variant	SPTAN1	GRCh38.p7	9:128568499	AAAATTATTAATAGG[A/T]TATTTTGTAGCATCT	6709
rs143101249	in-del	-/T	0.0158469	0.0875917	intron-variant	SPTAN1	GRCh38.p7	9:128603442	ATCCCTTTAAGGTAA[-/T]TTGGGTTAATCACAG	6709
rs143108250	snp	A/T	0.000477732	0.0154479	SPTAN1	9	allele_origin=T(germline)/A(germline)	9:128607904	TCCAGGCATTTGAGC[A/T]GTTTGGACAGCAGCT	6709
rs143116668	snp	A/G	0.000399281	0.0141238	intron-variant	SPTAN1	GRCh38.p7	9:128586335	ACAGGGTCTCGCTAT[A/G]TTGTCCCATCTGGTT	6709
rs143166100	snp	C/G	0.00128431	0.0253082	missense	SPTAN1	GRCh38.p7	9:128607988	TTGACCAGGAGCGTG[C/G]AGACCTGGAGAAGGC	6709
rs143198445	snp	A/G	0.0345262	0.126772	intron-variant	SPTAN1	GRCh38.p7	9:128605673	ACATGGCGAAACCCT[A/G]TTTCTATTATAAAAT	6709
rs143217160	snp	C/G	0.000399281	0.0141238	intron-variant	SPTAN1	GRCh38.p7	9:128593875	TTACTGTGCTAAGCG[C/G]TTGGTTTCAGTCCCT	6709
rs143288401	snp	C/G	0.000399281	0.0141238	intron-variant	SPTAN1	GRCh38.p7	9:128556558	GATAGTATTTGGGAA[C/G]CAATCAGAAGTAAGT	6709
rs143309753	snp	A/G/T	8.23749e-05	0.00641728	missense	SPTAN1	GRCh38.p7	9:128594296	AATGAGAAGGAAGCC[A/G/T]CTCTGACAAGTGAGG	6709
rs143348073	snp	A/C	0.00159617	0.0282053	intron-variant	SPTAN1	GRCh38.p7	9:128578626	ATGAGGTCAAGAGAT[A/C]AAGACCATCCATGCC	6709
rs143362484	snp	A/G	0.00755907	0.0610114	intron-variant	SPTAN1	GRCh38.p7	9:128598074	CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC	6709
rs143392181	snp	A/G	0.00221155	0.0331795	intron-variant	SPTAN1	GRCh38.p7	9:128632745	AAGGCCAGGTGCTGT[A/G]AGCCTCTGCCCGGGG	6709
rs143463331	snp	A/G	0.00517822	0.0506191	intron-variant	SPTAN1	GRCh38.p7	9:128565295	ACTGAGCGAGACTCC[A/G]TCTCAAACAAAAAAC	6709
rs143602636	snp	A/G	0.000399281	0.0141238	intron-variant	SPTAN1	GRCh38.p7	9:128586638	ACACATGTACATACC[A/G]GTGCGCACATATACC	6709
rs143633226	snp	A/G	1.66396e-05	0.00288436	synonymous-codon	SPTAN1	GRCh38.p7	9:128624432	GGCGAAGCTGGATGA[A/G]AACTCGGCCTTCCTT	6709
rs143675512	snp	A/G	0.000217037	0.010415	intron-variant	SPTAN1	GRCh38.p7	9:128627515	TGCCAGCCCGCTGGG[A/G]CCGGGGAGCAGCAGC	6709
rs143693467	snp	A/G	0.00953873	0.0683987	intron-variant	SPTAN1	GRCh38.p7	9:128597019	ACAAAAATTAGCTGG[A/G]CGTGGTAGCGCCTGC	6709
rs143698001	snp	C/T	0.000399281	0.0141238	intron-variant	SPTAN1	GRCh38.p7	9:128589913	CTACAAGCTACATCT[C/T]AGCCCAGCAGATCAT	6709
rs143734990	snp	C/T	0.00795532	0.062565	intron-variant	SPTAN1	GRCh38.p7	9:128599540	AGAGATAGGGTCTTG[C/T]TTTGTTGCCCAGACT	6709
rs143739246	snp	A/G	1.66194e-05	0.00288261	missense	SPTAN1	GRCh38.p7	9:128632896	GAGGAGATTGAGAGC[A/G]CCTTCCGGGCCCTCA	6709
rs143741474	snp	C/T	0.00716266	0.059414	intron-variant	SPTAN1	GRCh38.p7	9:128564247	AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT	6709
rs143761114	snp	A/G	0.000798403	0.0199641	intron-variant	SPTAN1	GRCh38.p7	9:128562733	ACTTTGGGAGGCCAA[A/G]GTGGGCGGATCACGA	6709
rs143781649	snp	A/G	0.0023933	0.0345097	intron-variant	SPTAN1	GRCh38.p7	9:128631866	CCTGGAGTCCTCGCC[A/G]TACTTGTCCTTGGCG	6709
rs143782878	snp	C/T	0.0170251	0.090679	intron-variant	SPTAN1	GRCh38.p7	9:128616193	ATGTCAGTCTACTGA[C/T]TCCAGTTGATGTGGC	6709
rs143844598	snp	C/T	0.000577277	0.0169795	SPTAN1	9	allele_origin=T(germline)/C(germline)	9:128605343	GATCCAGTCCCATCC[C/T]GAGTCAGCAGAAGAC	6709
rs143846397	snp	A/G	0.000399281	0.0141238	intron-variant	SPTAN1	GRCh38.p7	9:128577739	CTGCATCACTGCATT[A/G]TGATTGATAGAATGG	6709
rs143939145	snp	C/T	1.65411e-05	0.00287581	synonymous-codon	SPTAN1	GRCh38.p7	9:128585959	CAAGGACGAAGACTC[C/T]GCTGAGGTAACCAGG	6709
rs143941068	snp	C/T	0.000708408	0.018807	SPTAN1	9	allele_origin=T(germline)/C(germline)	9:128582780	TCTGCAGCAGTTTTT[C/T]CGTGATTCTGATGAG	6709
rs143969764	snp	C/T	0.0010396	0.0227754	SPTAN1	9	allele_origin=T(germline)/C(germline)	9:128617624	CTGACTGTGCTGTTT[C/T]CCATCTCTCATTCAG	6709
rs144000726	snp	A/C	0.000153988	0.00877328	synonymous-codon	SPTAN1	GRCh38.p7	9:128584287	GCATTCCCAGGACCG[A/C]ATTGATGGCATCACC	6709
rs144007463	snp	C/T	1.6898e-05	0.00290667	downstream-variant-500B, synonymous-codon	SPTAN1, WDR34	GRCh38.p7	9:128633756	CCCTCAGGCCGCCAC[C/T]TCTGCTGCCAGGCAG	6709
rs144030667	snp	A/G	0.0349115	0.127424	intron-variant	SPTAN1	GRCh38.p7	9:128621619	ACCCTGACACCACAC[A/G]TTAGATCTTTGTGTC	6709
rs144040647	snp	A/G	0.000399281	0.0141238	intron-variant	SPTAN1	GRCh38.p7	9:128580276	ACAGAGTGAGACCCT[A/G]TCTCTAAAAAAAAAT	6709
rs144062523	snp	C/T	0.000798403	0.0199641	intron-variant	SPTAN1	GRCh38.p7	9:128586050	GGAGAAGTAGTGATG[C/T]GCGGGAGGTGTGCAT	6709
rs144089278	snp	A/G	0.00159617	0.0282053	intron-variant	SPTAN1	GRCh38.p7	9:128599443	CCCAGCCCAGAAATT[A/G]ATTTCTATTTGCCAT	6709
rs144137515	snp	A/G	0.000399281	0.0141238	intron-variant	SPTAN1	GRCh38.p7	9:128611236	GAACTTTGGGAGGCC[A/G]ATGTGGCTCGATTGC	6709
rs144171907	snp	C/T	0.00478085	0.0486577	intron-variant	SPTAN1	GRCh38.p7	9:128558632	TTCCCAGATTTTTCC[C/T]TTCTGGTGCTCTCAA	6709
rs144248088	snp	A/G	0.000798403	0.0199641	intron-variant	SPTAN1	GRCh38.p7	9:128603113	AACCCAGTAACTATA[A/G]TTGGAGATGAAAGTG	6709
rs144279732	snp	A/C			intron-variant	SPTAN1	GRCh38.p7	9:128606393	AAAAAAAAAAAAAAA[A/C]AAGTCTCTACTTTCC	6709
rs144288438	snp	A/G	0.0345262	0.126772	intron-variant	SPTAN1	GRCh38.p7	9:128603110	AGCAACCCAGTAACT[A/G]TAATTGGAGATGAAA	6709
rs144289764	snp	A/G	0.000187395	0.00967794	missense	SPTAN1	GRCh38.p7	9:128626599	TGGACCGCCAGATCA[A/G]GAGCTTCCGCGTAGC	6709
rs144328905	snp	G/T	0.000399281	0.0141238	intron-variant	SPTAN1	GRCh38.p7	9:128566234	GCTATTTTTTTGTAT[G/T]TTTAGTAGAGACGGT	6709
rs144365799	snp	A/G			intron-variant	SPTAN1	GRCh38.p7	9:128589822	CCTCGTGATCCACCC[A/G]CCTCAGCCTCCCAAA	6709
rs144381596	snp	C/G	0.00398564	0.0444627	intron-variant	SPTAN1	GRCh38.p7	9:128587515	GTGCAACTGAGAAAG[C/G]CTGTTGAGGCAGGAT	6709
rs144435438	snp	C/T	0.000349415	0.0132131	SPTAN1	9	allele_origin=T(germline)/C(germline)	9:128621214	CGTCCACAAGGATCG[C/T]GTGAATGATGTCTGC	6709
rs144456039	snp	C/T	0.000399281	0.0141238	intron-variant	SPTAN1	GRCh38.p7	9:128629096	CCCCTCCCTTTGGTG[C/T]ATTCATTTGGTTTCT	6709
rs144458407	snp	A/G	0.000153988	0.00877328	missense	SPTAN1	GRCh38.p7	9:128617755	GCGCATGAGCCGGCT[A/G]TTCAGGTAAGGAGGC	6709
rs144489058	snp	G/T	1.64727e-05	0.00286986	missense	SPTAN1	GRCh38.p7	9:128591522	CAGGGTTTTGTGCCG[G/T]CTGCGTACGTGAAGA	6709
rs144590741	snp	C/G	0.000181379	0.00952138	missense	SPTAN1	GRCh38.p7	9:128580960	AGCGGCGCTGCTGGA[C/G]CTGTGGGAGCTGCGC	6709
rs144630244	snp	A/T			intron-variant	SPTAN1	GRCh38.p7	9:128623647	TTTTTTTTTTTTTGT[A/T]TTTTTTAGAAGAGAC	6709
rs144649618	snp	C/T	0.000214938	0.0103645	missense	SPTAN1	GRCh38.p7	9:128584412	AGGAGCCCATGGTTG[C/T]CCGGAAGCAGAAGCT	6709
rs144725581	snp	A/G	0.000632883	0.0177775	intron-variant	SPTAN1	GRCh38.p7	9:128626699	CAAGGTACACCTCCC[A/G]CTGCCCTCAGGAGCT	6709
rs144787939	snp	G/T	0.00536875	0.0515321	SPTAN1	9	allele_origin=G(germline)/T(germline)	9:128579718	GCTGGTCACTATGCC[G/T]CAGATGAAGTGAGGG	6709
rs144804532	snp	G/T	1.64727e-05	0.00286986	missense	SPTAN1	GRCh38.p7	9:128607650	GGGTTGGTGTCCTCA[G/T]ATGAGCTAGCCAAGG	6709
rs144819148	snp	C/T	0.0337553	0.125452	intron-variant	SPTAN1	GRCh38.p7	9:128620442	AGACCTGGGGCCAGG[C/T]GCGGTGGCTCACACC	6709
rs144840530	snp	G/T	0.000798403	0.0199641	intron-variant	SPTAN1	GRCh38.p7	9:128584076	GGAGGGATGAAATGT[G/T]TTGATTTTCTTAGAT	6709
rs144848474	snp	A/G	0.00478085	0.0486577	intron-variant	SPTAN1	GRCh38.p7	9:128606766	GCTGGGATTACAGGC[A/G]TGAGCCACTGCGCCT	6709
rs144899430	snp	C/T	0.000399281	0.0141238	intron-variant	SPTAN1	GRCh38.p7	9:128582036	TTCACAAGGATGACA[C/T]GCTATCTCGTTGAAG	6709
rs144919243	snp	C/T	0.000399281	0.0141238	intron-variant	SPTAN1	GRCh38.p7	9:128574004	GTGCTCTGCCCGCCT[C/T]GGCCTCCCAAAGTGC	6709
rs144953647	snp	A/G	0.000399281	0.0141238	intron-variant	SPTAN1	GRCh38.p7	9:128612458	AGTGGCACTTGGACT[A/G]CAGGTCACTCACATC	6709
rs145038571	snp	A/G	0.000873657	0.0208822	missense	SPTAN1	GRCh38.p7	9:128608962	TTTCTAGCCGGCGCA[A/G]TGAGGTCTTGGACAG	6709
rs145054594	snp	C/T	8.27109e-05	0.00643029	missense	SPTAN1	GRCh38.p7	9:128632846	AATACATGGCTTTCA[C/T]GATCAGCCGCGAAAC	6709
rs145060403	snp	A/C	0.0364509	0.129988	intron-variant	SPTAN1	GRCh38.p7	9:128589362	GGCACGATTTCAGCT[A/C]ACTGCAAGCTCCGCC	6709
rs145129059	snp	C/G	1.64887e-05	0.00287125	missense	SPTAN1	GRCh38.p7	9:128625802	CTGCAGGCCTTCCAG[C/G]AGGAAGGCATTGCCA	6709
rs145157002	snp	C/T	0.00119737	0.0244387	intron-variant	SPTAN1	GRCh38.p7	9:128628474	GGTAACAAGACTGTC[C/T]GCCCTAATAGAAGGC	6709
rs145163759	snp	C/G	0.0023933	0.0345097	intron-variant	SPTAN1	GRCh38.p7	9:128630967	GCCCGCCTCGGCCTC[C/G]CAAAGTGCTGGGATT	6709
rs145196379	snp	C/T	0.039522	0.134904	intron-variant	SPTAN1	GRCh38.p7	9:128622580	CTGGGATTACAGGCA[C/T]GAGCCACCACCCCCG	6709
rs145197328	snp	A/G	0.00159617	0.0282053	intron-variant	SPTAN1	GRCh38.p7	9:128575987	ATCTGCTTATAGGCT[A/G]GTACTTGTTTCCATT	6709
rs145232600	snp	A/G	0.000399281	0.0141238	intron-variant	SPTAN1	GRCh38.p7	9:128592633	AAAAAGATCAAATAC[A/G]TGGCTAAATTGCCTG	6709
rs145283248	snp	C/G	0.00716266	0.059414	intron-variant	SPTAN1	GRCh38.p7	9:128626045	GCCCACCTTCTGTCT[C/G]CCCAGCTCTGCCACT	6709
rs145292788	snp	C/T	0.00914312	0.0669923	intron-variant	SPTAN1	GRCh38.p7	9:128559626	AGATGCATAATTTCT[C/T]AATGTTTTTCCATCT	6709
rs145516440	snp	A/G	1.77685e-05	0.00298059	missense	SPTAN1	GRCh38.p7	9:128598433	TCACGGTTGAAGGAC[A/G]TTAACAAGGTAGCTG	6709
rs145551982	snp	A/G	0.000511716	0.0159874	missense	SPTAN1	GRCh38.p7	9:128608922	GACCAGCTCATCGCT[A/G]CCGGCCATTATGCCA	6709
rs145554993	snp	C/T	1.64727e-05	0.00286986	synonymous-codon	SPTAN1	GRCh38.p7	9:128575223	GTTACTTCTGAAGAG[C/T]TGGGCCAGGATCTGG	6709
rs145566452	snp	A/G	0.0112074	0.0740142	intron-variant	SPTAN1	GRCh38.p7	9:128613526	CCGAGTGCCTGGGAC[A/G]CAGCTCTGCCTGACT	6709
rs145582776	snp	A/G	0.000399281	0.0141238	intron-variant	SPTAN1	GRCh38.p7	9:128573216	CAGAATGCATCATCT[A/G]AGCTTGAATTGATTA	6709
rs145591902	snp	A/G	0.000798403	0.0199641	intron-variant	SPTAN1	GRCh38.p7	9:128622220	GACACACACCCAGAC[A/G]ACATTCTCTGTTCTT	6709
rs145636327	snp	A/C	0.00159617	0.0282053	intron-variant	SPTAN1	GRCh38.p7	9:128586448	CATTTTTCACTTTTT[A/C]TTATGAAAATGTAAT	6709
rs145733227	snp	C/T	1.65976e-05	0.00288072	missense	SPTAN1	GRCh38.p7	9:128624407	TGGAGAAAGCTGCAG[C/T]CCAGAGAAAGGCGAA	6709
rs145747686	snp	C/T	0.00159617	0.0282053	intron-variant	SPTAN1	GRCh38.p7	9:128626749	TCTCTGGGCCCTGCT[C/T]AGAGCCCACACTTAA	6709
rs145831552	snp	C/T	0.0023933	0.0345097	intron-variant	SPTAN1	GRCh38.p7	9:128601539	CCAGCCTGGGCAACA[C/T]GGCAAAACCCCGGCT	6709
rs145853891	snp	G/T	0.00199481	0.0315187	intron-variant	SPTAN1	GRCh38.p7	9:128598706	CTTGGTTTGGAGGGG[G/T]GTGGGGGCTTCTGTC	6709
rs145870898	snp	C/T	0.000131911	0.00812022	synonymous-codon	SPTAN1	GRCh38.p7	9:128583801	AGGAATAAAGCTTCG[C/T]GAAGCCAACCAGCAA	6709
rs145880441	snp	A/G	0.00119737	0.0244387	intron-variant	SPTAN1	GRCh38.p7	9:128594852	TTTCCTTTTGAGACA[A/G]AGTCTCTCTTTTGTC	6709
rs145893135	snp	C/G	0.00318978	0.0398085	intron-variant	SPTAN1	GRCh38.p7	9:128601950	TCTTCCCTTTTCTTA[C/G]GTAGCAAAACTTGGT	6709
rs145905190	snp	A/G	0.0271762	0.113356	intron-variant	SPTAN1	GRCh38.p7	9:128597806	CAGGCGCCTGCCACC[A/G]CGCCTAGCTAATTTT	6709
rs145913290	snp	A/G	4.94401e-05	0.00497168	missense	SPTAN1	GRCh38.p7	9:128611811	ACTCCCTCATTGAAC[A/G]TGGAGCCTGTGCCGG	6709
rs145971007	snp	C/T	0.00953873	0.0683987	intron-variant	SPTAN1	GRCh38.p7	9:128588600	ACACGTATGAGCCAC[C/T]GTGCCCAGACAAAAT	6709
rs146011840	snp	C/T	0.0345262	0.126772	intron-variant	SPTAN1	GRCh38.p7	9:128573473	CTTTTTTATTTTTCC[C/T]GAGATGGATTCTTGT	6709
rs146092668	snp	C/T	0.00953873	0.0683987	intron-variant	SPTAN1	GRCh38.p7	9:128569986	ATTCCAAATGTCATA[C/T]GACTAATAACATTTA	6709
rs146131723	snp	C/T	0.0337553	0.125452	intron-variant	SPTAN1	GRCh38.p7	9:128623975	TTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG	6709
rs146150071	snp	G/T	0.00019771	0.00994062	synonymous-codon	SPTAN1	GRCh38.p7	9:128607965	GATCAAGCAGAAACT[G/T]GATATTCTTGACCAG	6709
rs146153626	snp	C/T	0.000247139	0.0111134	missense	SPTAN1	GRCh38.p7	9:128605117	ATGATCTCGCCAGTG[C/T]CCAGGCCCTGCAACG	6709
rs146199583	snp	A/T	0.00358779	0.0422022	intron-variant	SPTAN1	GRCh38.p7	9:128617265	AAGTGTGTATATATG[A/T]ATATATATAAATATC	6709
rs146256117	snp	G/T	0.0441095	0.141807	intron-variant	SPTAN1	GRCh38.p7	9:128605851	ACAAAAATTAGCCAG[G/T]TGTGGTGGCAGGCAT	6709
rs146377338	snp	A/G	0.0236746	0.106192	intron-variant	SPTAN1	GRCh38.p7	9:128590484	CGAGACAGGAGGATC[A/G]CTTGAGCCCAGGAGT	6709
rs146388308	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	SPTAN1	GRCh38.p7	9:128552378	CTCACCTCTTCCCCC[A/G]CATTGTCGCTTCGGC	6709
rs146412583	snp	A/G	6.60055e-05	0.00574442	missense	SPTAN1	GRCh38.p7	9:128584313	TCACCATTCAGGCCC[A/G]CCAGTTCCAAGATGC	6709
rs146418243	snp	C/T	4.94694e-05	0.00497316	synonymous-codon	SPTAN1	GRCh38.p7	9:128617673	GGGCTCAGAGGACTA[C/T]GGCCGGGACCTAACC	6709
rs146432265	snp	C/T	0.00874735	0.0655527	intron-variant	SPTAN1	GRCh38.p7	9:128619341	GTACCACAGACAGAG[C/T]GGCACAGATGGAGTG	6709
rs146442842	in-del	-/T			intron-variant	SPTAN1	GRCh38.p7	9:128606665	ATTTTGTATTTTTTT[-/T]AGTAGAGGCGGGGTT	6709
rs146443854	snp	A/G	0.000399281	0.0141238	intron-variant	SPTAN1	GRCh38.p7	9:128586053	GAAGTAGTGATGCGC[A/G]GGAGGTGTGCATTAC	6709
rs146507720	snp	C/T	0.000798403	0.0199641	intron-variant	SPTAN1	GRCh38.p7	9:128582931	ATTGTAGCTAAAGGA[C/T]GAAATAAGGGATTCC	6709
rs146535920	snp	A/C	3.34661e-05	0.00409047	synonymous-codon	SPTAN1	GRCh38.p7	9:128632282	GCTGGACCAGCTGGG[A/C]ATGCGCATGCAGCAC	6709
rs146537034	snp	C/T	0.0422008	0.138995	intron-variant	SPTAN1	GRCh38.p7	9:128623424	CAAAAATAATACTAA[C/T]GAATATATCATCTTA	6709
rs146585813	snp	C/T	0.000399281	0.0141238	intron-variant	SPTAN1	GRCh38.p7	9:128586902	GGATAACTGCAACCT[C/T]CACCTCCTGGGTTCA	6709
rs146659590	snp	A/G	0.000798403	0.0199641	intron-variant	SPTAN1	GRCh38.p7	9:128608507	AAAACAAATGTGTGG[A/G]TAGGTAAGGGAATAA	6709
rs146678096	snp	G/T			intron-variant	SPTAN1	GRCh38.p7	9:128613003	AACCATTCCCATATT[G/T]TTGGACATTGAGGTG	6709
rs146784753	snp	A/G	0.000399281	0.0141238	intron-variant	SPTAN1	GRCh38.p7	9:128594067	CATCATTACAAACTC[A/G]TAGCCTGGAATCCAC	6709
rs146807067	snp	A/G	0.00636936	0.0560724	intron-variant	SPTAN1	GRCh38.p7	9:128599604	GCCTACTGCAGCCTC[A/G]AACTCTTGGCCTCAA	6709
rs146858285	in-del	-/A	0.0759472	0.179459	intron-variant	SPTAN1	GRCh38.p7	9:128606487	CATATATATATATAT[-/A]TTTTTTTTTTGGGGG	6709
rs146869468	snp	A/G	0.0337553	0.125452	intron-variant	SPTAN1	GRCh38.p7	9:128631369	GAGGCTGAGGCAGGA[A/G]AATCACTTGATTCTG	6709
rs146951548	snp	C/G/T	0.00159617	0.0282053	intron-variant	SPTAN1	GRCh38.p7	9:128565026	AAGGAAGCCATAGGT[C/G/T]GGGGGCAGTGGCTCA	6709
rs147062700	snp	A/G	0.00159617	0.0282053	intron-variant	SPTAN1	GRCh38.p7	9:128618553	CAGTGGCACAATCTC[A/G]GCTCACTGCAAGCTC	6709
rs147132904	snp	A/C/T	0.00130314	0.0254928	SPTAN1	9	allele_origin=T(germline)/C(germline)	9:128625933	TCTGGCCAACTCAGC[A/C/T]GCCCGCAAGAAGAAG	6709
rs147149360	snp	A/G	4.96816e-05	0.00498381	missense, downstream-variant-500B	SPTAN1, WDR34	GRCh38.p7	9:128633230	ACCCGGGAACAAGCC[A/G]ACTACTGCGTCTCCC	6709
rs147151976	snp	A/G	0.0142736	0.0832652	intron-variant	SPTAN1	GRCh38.p7	9:128596341	GAGTGCAGTGGCGCA[A/G]TCTCGGCTCACTGCA	6709
rs147207084	snp	C/T	0.000798403	0.0199641	intron-variant	SPTAN1	GRCh38.p7	9:128629804	TCTCCCAGCACTCCA[C/T]TTGTGTCCTTTGTCT	6709
rs147223529	snp	C/G/T	6.6138e-05	0.00575024	synonymous-codon	SPTAN1	GRCh38.p7	9:128632820	TAGAGATGGCCATGT[C/G/T]TCCTTGCAAGAATAC	6709
rs147233101	snp	C/T	0.000346178	0.0131518	SPTAN1	9	allele_origin=T(germline)/C(germline)	9:128605401	CAGGCCTGGAGCAGC[C/T]TGGGGAAACGTGCAG	6709
rs147262142	in-del	-/CAA			intron-variant	SPTAN1	GRCh38.p7	9:128594824	TTTTTTTTTTTTTTT[-/CAA]TTTTTTTTTTTTTCC	6709
rs147309773	snp	A/G	0.338069	0.233974	intron-variant	SPTAN1	GRCh38.p7	9:128559798	AGAGTGCAGTGGTGC[A/G]ATCTTGGCTCACTGC	6709
rs147314498	snp	C/G	0.00159617	0.0282053	intron-variant	SPTAN1	GRCh38.p7	9:128611528	TTCCTTCCTCCTTTG[C/G]TAACTCCCCAAGAGA	6709
rs147331091	snp	C/T	0.00358779	0.0422022	intron-variant	SPTAN1	GRCh38.p7	9:128616350	CTCGAGCTGACCTCA[C/T]CTGACCTCAAGTGAT	6709
rs147363275	snp	A/G	0.0441095	0.141807	intron-variant	SPTAN1	GRCh38.p7	9:128562283	AATTTTTGTATTTTT[A/G]GTAGAGATGTGGTTT	6709
rs147431730	snp	A/G	0.000798403	0.0199641	intron-variant	SPTAN1	GRCh38.p7	9:128558763	CAGCATGCAGCCTCG[A/G]TTGTGGAAGGAATGT	6709
rs147432108	snp	A/G	0.00835141	0.0640778	intron-variant	SPTAN1	GRCh38.p7	9:128599135	TGGAAAACTCCAAAA[A/G]TTGATTTCTTTTTTT	6709
rs147444364	snp	G/T	1.64727e-05	0.00286986	missense	SPTAN1	GRCh38.p7	9:128581854	AAGAAGCACGAAGAC[G/T]TTGAGAAATCCCTTA	6709
rs147464432	snp	A/G			intron-variant	SPTAN1	GRCh38.p7	9:128610280	CAAAGTTACTTAAGC[A/G]GGTGGAAGAAATGAA	6709
rs147466898	snp	C/T	0.00059313	0.0172108	SPTAN1	9	allele_origin=T(germline)/C(germline)	9:128585887	CTTTGCTGATGCTAA[C/T]GAGGCTGAATCCTGG	6709
rs147591945	snp	A/G	0.000798403	0.0199641	intron-variant	SPTAN1	GRCh38.p7	9:128572434	TCAGACACATCAGCA[A/G]TGGGACAATGGTTCC	6709
rs147609987	snp	C/T	0.00119737	0.0244387	intron-variant	SPTAN1	GRCh38.p7	9:128623406	GATTCAGTTTTTTTC[C/T]ATCAAAAATAATACT	6709
rs147626525	snp	A/C/T	0.00358779	0.0422022	intron-variant	SPTAN1	GRCh38.p7	9:128626173	CGCCATTCAGAAGCA[A/C/T]GCAGGACAGACTAGA	6709
rs147696217	snp	A/G	0.00795532	0.062565	intron-variant	SPTAN1	GRCh38.p7	9:128556286	GTCTTTGTTTTCTAA[A/G]TCGGACCTTTTTCAC	6709
rs147708363	snp	A/G	0.000439464	0.0148168	synonymous-codon	SPTAN1	GRCh38.p7	9:128575279	ATTTGAAGAGTTTCA[A/G]ACAGATATGGCTGCT	6709
rs147717209	snp	C/T	0.00914312	0.0669923	intron-variant	SPTAN1	GRCh38.p7	9:128604127	AGGTGTTTGTGGGTG[C/T]TGAAGCTGTCAAGCA	6709
rs147727119	snp	C/T	0.000798403	0.0199641	intron-variant	SPTAN1	GRCh38.p7	9:128568188	TTTAACTATAAAAAA[C/T]TGATTACAGTAACCT	6709
rs147731264	snp	C/T	0.0345262	0.126772	intron-variant	SPTAN1	GRCh38.p7	9:128607179	TTTCTTTTTTTTCTT[C/T]TTTTTTTAGAGACAG	6709
rs147736685	snp	A/G	0.000399281	0.0141238	intron-variant	SPTAN1	GRCh38.p7	9:128571151	AAAAATTAGTGGGGC[A/G]TGGTGGTGCACACCT	6709
rs147815147	snp	C/T	3.38776e-05	0.00411554	synonymous-codon	SPTAN1	GRCh38.p7	9:128621244	CACCAATGGACAAGA[C/T]CTCATTAAGAAGGTG	6709
rs147831220	snp	C/T	0.00159617	0.0282053	intron-variant	SPTAN1	GRCh38.p7	9:128591365	GCCACTGTGGCCGGC[C/T]GTTTTGGACCTCTTA	6709
rs147900000	snp	C/T	0.000153988	0.00877328	missense	SPTAN1	GRCh38.p7	9:128574715	AGTGGGAATTACTTT[C/T]GGAGAAGATGCGAGA	6709
rs148096063	snp	C/G	0.00279162	0.0372561	intron-variant	SPTAN1	GRCh38.p7	9:128589926	CTCAGCCCAGCAGAT[C/G]ATTGAAGACAGCTGT	6709
rs148101726	snp	C/T	0.000399281	0.0141238	intron-variant	SPTAN1	GRCh38.p7	9:128577671	TTGGAGACTGGCAAC[C/T]GTATCATGTGTAGTA	6709
rs148133620	snp	A/G	0.00384746	0.0436912	intron-variant	SPTAN1	GRCh38.p7	9:128632083	TGGGCTGGTGACTGA[A/G]CTGAGGGCCCCCGTC	6709
rs148141481	snp	A/G	0.0150606	0.0854603	intron-variant	SPTAN1	GRCh38.p7	9:128620507	AGATCACCTGAGGTC[A/G]GGAGTCCGAGACCAA	6709
rs148173166	snp	C/T	1.67298e-05	0.00289217	missense	SPTAN1	GRCh38.p7	9:128632933	AGGGAAAGCCTTACG[C/T]GACCAAGGAGGAGCT	6709
rs148191776	snp	C/T	0.000399281	0.0141238	intron-variant	SPTAN1	GRCh38.p7	9:128568510	TAGGATATTTTGTAG[C/T]ATCTTCCATTGACAA	6709
rs148191896	in-del	-/A	0.0345262	0.126772	intron-variant	SPTAN1	GRCh38.p7	9:128608453	AGATTTTAATAATGG[-/A]GGGTGCCACAGGAAA	6709
rs148258493	snp	C/T	3.30808e-05	0.00406686	missense	SPTAN1	GRCh38.p7	9:128584414	GAGCCCATGGTTGCC[C/T]GGAAGCAGAAGCTGG	6709
rs148294757	snp	A/G	0.000153988	0.00877328	missense	SPTAN1	GRCh38.p7	9:128615689	ACCAGCAGTGCCTTC[A/G]ACACCTCCCAAGTAA	6709
rs148306403	snp	A/T	0.000399281	0.0141238	intron-variant	SPTAN1	GRCh38.p7	9:128556570	GAAGCAATCAGAAGT[A/T]AGTTTTCTCAATATT	6709
rs148359051	snp	A/G	0.029116	0.117091	intron-variant	SPTAN1	GRCh38.p7	9:128561096	ATATGTCGGCCAGGC[A/G]CGGTGGTTCACGCCT	6709
rs148402616	snp	C/T	4.95381e-05	0.0049766	missense	SPTAN1	GRCh38.p7	9:128618053	GAGGAGATCCAGCAG[C/T]GGCTGGCGCAGTTTG	6709
rs148417918	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	SPTAN1	GRCh38.p7	9:128554625	CCTTTGTAATCAGTC[C/T]TCCGTGGGCTATGCA	6709
rs148439588	snp	A/G	0.0103295	0.0711199	intron-variant	SPTAN1	GRCh38.p7	9:128579803	AAGTCTCTGAAAGCT[A/G]TTATTCATCCTTAAA	6709
rs148453112	snp	A/G	0.00081588	0.020181	downstream-variant-500B, intron-variant	SPTAN1, WDR34	GRCh38.p7	9:128634030	AAACTCTAGAGACCA[A/G]CCACATGGCAGGAGG	6709
rs148461252	snp	G/T	0.0103295	0.0711199	intron-variant	SPTAN1	GRCh38.p7	9:128596718	TTTTTTAGAGATAGG[G/T]TCTCACTCTCTCACA	6709
rs148496048	in-del	-/ATA	0.00199481	0.0315187	intron-variant	SPTAN1	GRCh38.p7	9:128624740	GCACGCAGAGATGGC[-/ATA]ATGTGACGTCATGGC	6709
rs148502349	snp	A/G	0.000399281	0.0141238	intron-variant	SPTAN1	GRCh38.p7	9:128571117	ACATAGTGAGACCTC[A/G]TCTCTACAAAAAAAA	6709
rs148554113	snp	C/T	0.000197658	0.00993931	synonymous-codon	SPTAN1	GRCh38.p7	9:128607673	AGCCAAGGATGTCAC[C/T]GGAGCTGAGGCATTG	6709
rs148574836	snp	A/G	0.00478085	0.0486577	intron-variant	SPTAN1	GRCh38.p7	9:128584216	AAAAAGACCTTATCA[A/G]TTTTTCTCTGTATAC	6709
rs148612219	snp	C/T	0.000399281	0.0141238	intron-variant	SPTAN1	GRCh38.p7	9:128625084	GAGGGCAGTATATTT[C/T]CCACACTTCGTTTTC	6709
rs148615817	snp	C/T	0.00159617	0.0282053	intron-variant	SPTAN1	GRCh38.p7	9:128558174	GATCTGGTAGTATTG[C/T]AAGAATGCTGACAAG	6709
rs148669182	snp	A/C	0.000798403	0.0199641	intron-variant	SPTAN1	GRCh38.p7	9:128562780	CCATCCTGGCTAGCA[A/C]GGTGAAACGCCATCT	6709
rs148693978	snp	C/T	0.000367905	0.0135579	downstream-variant-500B, synonymous-codon	SPTAN1, WDR34	GRCh38.p7	9:128633804	CCGGGGCCCTTGTTC[C/T]GTGAACTCTGTGCTC	6709
rs148727077	snp	C/T	0.00238571	0.0344552	missense	SPTAN1	GRCh38.p7	9:128581831	TGGATAGTGTGGAAG[C/T]GCTTCTTAAGAAGCA	6709
rs148787277	snp	A/G	0.0166325	0.0896639	intron-variant	SPTAN1	GRCh38.p7	9:128616611	GTCTCTACTAAATAC[A/G]CAAAAATTAGCCAGG	6709
rs148814010	in-del	-/C	0.00119737	0.0244387	intron-variant	SPTAN1	GRCh38.p7	9:128631810	GGCGACAGTGAGACT[-/C]CCATCTCAAAAAAAT	6709
rs148814385	snp	A/G	0.000399281	0.0141238	intron-variant	SPTAN1	GRCh38.p7	9:128573025	GTTGACTGTCACATG[A/G]TTTTCAGGTTTTCAT	6709
rs148881922	snp	A/G	0.0337553	0.125452	intron-variant	SPTAN1	GRCh38.p7	9:128622521	TCAGGCTGGTCTCGA[A/G]CTCCTGACCTCAGGT	6709
rs148914024	snp	A/G	0.00199481	0.0315187	intron-variant	SPTAN1	GRCh38.p7	9:128586567	TGTGCTTACATACAT[A/G]CTAACATACCAACAT	6709
rs148933269	snp	C/T	0.0221141	0.102801	intron-variant	SPTAN1	GRCh38.p7	9:128627241	CCAAGTGCTCTGAGC[C/T]GGCCTCATGTCTCCC	6709
rs148981489	snp	C/T	0.0603597	0.1629	intron-variant	SPTAN1	GRCh38.p7	9:128564173	CGCCTGTAATCTTAG[C/T]ACTTTGGGAGGCCAA	6709
rs148984013	snp	C/T	8.30585e-05	0.00644379	synonymous-codon	SPTAN1	GRCh38.p7	9:128632895	CGAGGAGATTGAGAG[C/T]GCCTTCCGGGCCCTC	6709
rs149024655	snp	A/T	0.00119737	0.0244387	intron-variant	SPTAN1	GRCh38.p7	9:128604959	AAATAAATAAATAAA[A/T]AAATTTTTTTTAGTG	6709
rs149176069	snp	A/C/T	0.029116	0.117091	intron-variant	SPTAN1	GRCh38.p7	9:128556288	CTTTGTTTTCTAAGT[A/C/T]GGACCTTTTTCACAA	6709
rs149193470	snp	C/T	0.00597247	0.0543191	intron-variant	SPTAN1	GRCh38.p7	9:128598058	GGTTCAAGCGATTCT[C/T]CTGCCTCAGCCTCCC	6709
rs149228783	snp	A/G	0.000153988	0.00877328	missense	SPTAN1	GRCh38.p7	9:128575286	GAGTTTCAAACAGAT[A/G]TGGCTGCTCATGAAG	6709
rs149289060	snp	C/T	0.00517616	0.0506092	SPTAN1	9	allele_origin=T(germline)/C(germline)	9:128577336	GGAGAATAGTTCTGA[C/T]GGAGTTCATTTCTAG	6709
rs149318543	snp	A/G	0.000743427	0.0192655	synonymous-codon, downstream-variant-500B	SPTAN1, WDR34	GRCh38.p7	9:128633292	CGAGCTCCCCACCGC[A/G]TTCGACTACGTGGAG	6709
rs149336930	snp	A/C/T	6.59701e-05	0.00574296	missense	SPTAN1	GRCh38.p7	9:128580950	CCGAGGAGAGAGCGG[A/C/T]GCTGCTGGAGCTGTG	6709
rs149367932	snp	A/G	6.62482e-05	0.00575497	missense	SPTAN1	GRCh38.p7	9:128605477	TCCTTAGCGATTTCC[A/G]GTACGGAGCCATGTT	6709
rs149389417	snp	C/G	0.0345262	0.126772	intron-variant	SPTAN1	GRCh38.p7	9:128614265	TTCAAGACCAGCCTG[C/G]GCAACATGATGAGAC	6709
rs149442564	snp	A/G	0.000399281	0.0141238	intron-variant	SPTAN1	GRCh38.p7	9:128619825	CTAAATGTAGTGGTT[A/G]AAAGCAGCACCCATT	6709
rs149458689	snp	A/G	3.29891e-05	0.00406122	missense	SPTAN1	GRCh38.p7	9:128625922	TGGAGCCAGCTTCTG[A/G]CCAACTCAGCCGCCC	6709
rs149459276	snp	A/G	0.000399281	0.0141238	intron-variant	SPTAN1	GRCh38.p7	9:128568487	TAGCAAAAACAAAAA[A/G]TTATTAATAGGATAT	6709
rs149490642	snp	C/T	0.0126979	0.078662	intron-variant	SPTAN1	GRCh38.p7	9:128558094	AGGCGTGAGCCACCG[C/T]GCCCAGCTGTATATT	6709
rs149498163	snp	A/G/T	0.000660304	0.0181584	intron-variant	SPTAN1	GRCh38.p7	9:128609371	ATTTATAAAACAATC[A/G/T]CCTTGCACCCATGGG	6709
rs149528201	snp	C/T	1.64879e-05	0.00287118	missense	SPTAN1	GRCh38.p7	9:128585831	GCCAAAGCTTCCCAG[C/T]GTCGGCAGGACCTGG	6709
rs149647766	snp	A/G	0.000399281	0.0141238	intron-variant	SPTAN1	GRCh38.p7	9:128587155	CAGTGATGCAATCAC[A/G]ACTCCCTACAGCTTT	6709
rs149747513	snp	C/T	0.000399281	0.0141238	intron-variant	SPTAN1	GRCh38.p7	9:128622179	ATGTATAGATGTAGA[C/T]GTGGCTCCTGCACAC	6709
rs149764576	snp	A/G	0.0345262	0.126772	intron-variant	SPTAN1	GRCh38.p7	9:128606692	GGTTTCTCCATGTTG[A/G]TCAGGCTGGTCTCGA	6709
rs149775363	in-del	-/T	0.0345262	0.126772	intron-variant	SPTAN1	GRCh38.p7	9:128572834	TCCGAGTAGGTGGAG[-/T]TATTGACTTGGTTGC	6709
rs149806602	snp	A/G	0.000439271	0.0148136	missense	SPTAN1	GRCh38.p7	9:128566745	CATTTCAGAAAATGG[A/G]CCCAAGTGGGGTCAA	6709
rs149808299	snp	A/G	0.0162398	0.0886349	intron-variant	SPTAN1	GRCh38.p7	9:128559884	GGACTACAGGCGTGC[A/G]CCACTATGCTTGGCT	6709
rs149816850	snp	A/G	0.000399281	0.0141238	intron-variant	SPTAN1	GRCh38.p7	9:128612361	CAGACACCCCTTTTG[A/G]CAGAAACCCTTATTA	6709

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