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

SPSB1

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs473654	snp	C/T	0.26818	0.249338	intron-variant	SPSB1	GRCh38.p7	1:9351608	CTGGACTCGCCACCT[C/T]CCCTGGAACTGCAGC	80176
rs478103	snp	C/T	0.219648	0.248151	intron-variant	SPSB1	GRCh38.p7	1:9342344	GACAAGTCCAGAAAC[C/T]GTGTGCATCAGCCTG	80176
rs478552	snp	A/G	0.330249	0.23677	intron-variant	SPSB1	GRCh38.p7	1:9298420	aacgaatgaatgaat[A/G]agtgaacgaatgaat	80176
rs479043	snp	G/T	0.459347	0.136653	intron-variant	SPSB1	GRCh38.p7	1:9342461	GATCCCAGTGGCTTG[G/T]CAATTCGCTGATAGC	80176
rs482215	snp	C/T	0.00874735	0.0655527	intron-variant	SPSB1	GRCh38.p7	1:9347904	TGGGGAAAGGACACT[C/T]CTACACACTGTGGGT	80176
rs483823	snp	C/G	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9353154	AGAGCTGCATGGAGC[C/G]GGGGTGCAGAGTACC	80176
rs483934	snp	C/T	0.00874735	0.0655527	intron-variant	SPSB1	GRCh38.p7	1:9347744	ACCAAACCCTATAGG[C/T]CTGCACAGGGACATG	80176
rs483936	snp	C/G	0.453939	0.144598	intron-variant	SPSB1	GRCh38.p7	1:9347741	AAACCCTATAGGCCT[C/G]CACAGGGACATGAGG	80176
rs504357	snp	A/G	0.348354	0.22984	intron-variant	SPSB1	GRCh38.p7	1:9340093	CACAGACCATCACCC[A/G]GGAGCTTGCTGGAAA	80176
rs504358	snp	C/G	0.476052	0.106772	intron-variant	SPSB1	GRCh38.p7	1:9340096	CCAGCAAGCTCCTGG[C/G]TGATGGTCTGTGGGC	80176
rs507656	snp	C/G	0.498673	0.0257246	intron-variant	SPSB1	GRCh38.p7	1:9318653	AGGCACCAGCCACAC[C/G]GTCTGGCTTTGGTCA	80176
rs510666	snp	A/G	0.0287284	0.116357	intron-variant	SPSB1	GRCh38.p7	1:9343616	AGAAATGAAAATGTC[A/G]CTGTGTTTAGAGTGA	80176
rs513170	snp	C/T	0.0228947	0.104514	intron-variant	SPSB1	GRCh38.p7	1:9343872	catgaacccaggagg[C/T]ggagctttcagtgag	80176
rs515748	snp	A/C	0	0	intron-variant	SPSB1	GRCh38.p7	1:9361197	ttagagatggggtat[A/C]actatgttgcctagg	80176
rs522526	snp	C/T	0.457853	0.138915	intron-variant	SPSB1	GRCh38.p7	1:9315146	GGCTGAGAAGCTCAG[C/T]GGGGCTGGGACAAGA	80176
rs525476	snp	A/G	0.481932	0.0933148	intron-variant	SPSB1	GRCh38.p7	1:9315527	TCACATTCACATTCA[A/G]CTCCCACCCCGTCAT	80176
rs531796	snp	A/G	0.426813	0.17674	intron-variant	SPSB1	GRCh38.p7	1:9306366	CCTCCTCCAGGCTGG[A/G]CATCACAAAGGAAAA	80176
rs536073	snp	A/C	0.445328	0.156035	intron-variant	SPSB1	GRCh38.p7	1:9319471	GCCTCGGAGCCTCTC[A/C]TCCCACCCCTGTACT	80176
rs536211	snp	C/G	0.423257	0.180228	intron-variant	SPSB1	GRCh38.p7	1:9349407	ACTCACCTACCCCCA[C/G]TCCTGGCCCGGCACA	80176
rs543576	snp	C/T	0.375598	0.21616	intron-variant	SPSB1	GRCh38.p7	1:9365216	acagtggcacaatca[C/T]agcttactgcagcct	80176
rs544264	snp	C/T	0.219947	0.248187	intron-variant	SPSB1	GRCh38.p7	1:9344958	GTGCCAAGGCCTGAA[C/T]GGGAGCCAGTGACAC	80176
rs547506	snp	C/T	0.43221	0.171171	intron-variant	SPSB1	GRCh38.p7	1:9301947	ttggcagaagcactg[C/T]gtgcagggaagacga	80176
rs552230	snp	G/T	0.430136	0.173352	intron-variant	SPSB1	GRCh38.p7	1:9362816	CAGGCGCTATTTCTG[G/T]GAGCAGAAGCCTGAG	80176
rs553161	snp	A/G	0.270892	0.249126	intron-variant	SPSB1	GRCh38.p7	1:9362918	GCTATGCCCATCCCC[A/G]GGAAGCTTAGGCGCT	80176
rs554020	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9302639	agtctttggcctggg[A/C]ctgggaatgaccacg	80176
rs557573	snp	C/T	0.234692	0.249531	intron-variant	SPSB1	GRCh38.p7	1:9316737	TCCGGGGCGGTCTCC[C/T]CTGGAGAAGCAGCCG	80176
rs563317	snp	C/G	0.493477	0.0567349	intron-variant	SPSB1	GRCh38.p7	1:9297889	agacagatctttcac[C/G]catacgttgagaaat	80176
rs563347	snp	A/G	0.166832	0.235761	intron-variant	SPSB1	GRCh38.p7	1:9297901	cacgcatacgttgag[A/G]aatagatttgtgagg	80176
rs564709	snp	C/T	0.252421	0.249988	intron-variant	SPSB1	GRCh38.p7	1:9322226	AGACGATGCTGGTAC[C/T]CTACTCAGCCTGATG	80176
rs577685	snp	A/G	0.499995	0.00159744	intron-variant	SPSB1	GRCh38.p7	1:9302900	atcccctagggaccc[A/G]ctagcgaaattgttg	80176
rs581587	snp	A/G	0.34146	0.23267	intron-variant	SPSB1	GRCh38.p7	1:9306793	CAATCCCCATTACCT[A/G]GGACCACTTCTGACT	80176
rs602386	snp	C/G	0.391583	0.206044	intron-variant	SPSB1	GRCh38.p7	1:9345864	TATTTTTATATCCCT[C/G]CTTGAGGGGTCCCTC	80176
rs603590	snp	A/G	0.495671	0.0463237	intron-variant	SPSB1	GRCh38.p7	1:9318805	TGTCCCCCACTATAT[A/G]CAGTGAGTCCTTGGA	80176
rs617018	snp	C/T	0.445592	0.155704	intron-variant	SPSB1	GRCh38.p7	1:9318043	GGAAAGGGGAATGAG[C/T]GCAGCTGCTTCCTCT	80176
rs617901	snp	C/T	0.0248432	0.108648	intron-variant	SPSB1	GRCh38.p7	1:9317880	AAACTCCCACCAAAG[C/T]GACCCGCCAATCTGC	80176
rs618432	snp	A/G	0.0547245	0.156101	intron-variant	SPSB1	GRCh38.p7	1:9351159	aaatcaatgggcatg[A/G]atgtgtttcaataaa	80176
rs619224	snp	A/G	0.00597247	0.0543191	intron-variant	SPSB1	GRCh38.p7	1:9351037	ATTCCTGGACATGGC[A/G]CTCAGGACAGGGGGT	80176
rs619282	snp	A/G	0.276267	0.248616	intron-variant	SPSB1	GRCh38.p7	1:9351001	CCACCCACAGGTACC[A/G]AGTAACATTCACAGG	80176
rs619928	snp	C/T	0.484701	0.0861117	intron-variant	SPSB1	GRCh38.p7	1:9298622	gtaaccagttatccc[C/T]gaacaatctaattat	80176
rs621655	snp	A/G	0.357664	0.225629	intron-variant	SPSB1	GRCh38.p7	1:9365968	TGCGCGGCCCTGCTC[A/G]CCCGCTTCGCCAGAG	80176
rs621846	snp	A/G	0.493748	0.0555599	intron-variant	SPSB1	GRCh38.p7	1:9298184	aagtaagaatttcac[A/G]ggtttcctgtctatt	80176
rs622662	snp	C/G	0.493477	0.0567349	intron-variant	SPSB1	GRCh38.p7	1:9298026	tactgccacttggcc[C/G]ctgcactccaaatgc	80176
rs624927	snp	A/G	0.460813	0.134379	intron-variant	SPSB1	GRCh38.p7	1:9337484	GTTTGGGGACAGGAA[A/G]CCCTCTTTGGGGGGA	80176
rs628739	snp	C/T	0.453575	0.145111	intron-variant	SPSB1	GRCh38.p7	1:9311150	AAAAACCCTTTATCC[C/T]GCGCTGTCTAGACAC	80176
rs629524	snp	A/C	0.499954	0.00479211	intron-variant	SPSB1	GRCh38.p7	1:9311040	CACACTGACCAGCTC[A/C]AAATTGGCCCGATAG	80176
rs630075	snp	C/T	0.499961	0.0043928	intron-variant	SPSB1	GRCh38.p7	1:9310852	CTTCCCCAAGCTTCA[C/T]AAATGCAAGGCAACC	80176
rs631824	snp	C/T	0.0248432	0.108648	intron-variant	SPSB1	GRCh38.p7	1:9343865	ccaggaggcggagct[C/T]tcagtgagccgagat	80176
rs643762	snp	A/T	0.376989	0.215346	intron-variant	SPSB1	GRCh38.p7	1:9343512	GAGCCCAAATGTCCA[A/T]CAATGGATGCATGGA	80176
rs644728	snp	C/T	0.219947	0.248187	intron-variant	SPSB1	GRCh38.p7	1:9343244	GGAAGTGACAGAGGT[C/T]TCTTTTAGGGGTGAT	80176
rs658738	snp	G/T	0.459118	0.137002	intron-variant	SPSB1	GRCh38.p7	1:9342459	AGGATCCCAGTGGCT[G/T]GTCAATTCGCTGATA	80176
rs662553	snp	A/G	0.00874735	0.0655527	intron-variant	SPSB1	GRCh38.p7	1:9348236	TTAAAAAAAGTTGCc[A/G]cggtggctcacgcct	80176
rs663419	snp	A/G	0.00874735	0.0655527	intron-variant	SPSB1	GRCh38.p7	1:9348026	acccaggaggcggag[A/G]ttgcagtgagccgag	80176
rs664347	snp	A/G	0.282895	0.247826	intron-variant	SPSB1	GRCh38.p7	1:9347797	TGTGCAAAACGCCCA[A/G]CAATCACCCAGCAAC	80176
rs664623	snp	C/T	0.253824	0.249971	intron-variant	SPSB1	GRCh38.p7	1:9322298	GAACCTCAGTTTCCC[C/T]ACCTGCAAACCGAGG	80176
rs664730	snp	A/G	0.00914312	0.0669923	intron-variant	SPSB1	GRCh38.p7	1:9347724	GTCCCCAGCATCTTC[A/G]TCCTCATGTCCCTGT	80176
rs672453	snp	C/T	0.496937	0.0390173	intron-variant	SPSB1	GRCh38.p7	1:9301724	gagtggcagtccatg[C/T]tgctgagcccatgca	80176
rs732590	snp	C/T	0.439363	0.163222	intron-variant	SPSB1	GRCh38.p7	1:9329172	CTGCAGTGCCCCTCA[C/T]ACTGCTTCATACAAC	80176
rs732591	snp	A/G	0.409382	0.192607	intron-variant	SPSB1	GRCh38.p7	1:9329159	CACACTGCTTCATAC[A/G]ACTGCCCTTAGGTGT	80176
rs732592	snp	A/G	0.402454	0.198136	intron-variant	SPSB1	GRCh38.p7	1:9329112	TGGGAGGCTGTCCCC[A/G]CCACCCTGTCCCCCA	80176
rs733096	snp	C/T	0.179744	0.239925	intron-variant	SPSB1	GRCh38.p7	1:9341235	TGGTGGGGAGTGGTG[C/T]GTGTACCGTGCCTCT	80176
rs733892	snp	C/T	0.210605	0.246877	intron-variant	SPSB1	GRCh38.p7	1:9354338	AGGAGCCTGTGGGGG[C/T]GCCTGGGCGGGAGGC	80176
rs733893	snp	C/T	0.385359	0.210185	intron-variant	SPSB1	GRCh38.p7	1:9354950	GGGAGGAAAGTCCGA[C/T]GCTAGGATGCCTCGT	80176
rs909511	snp	C/T	0.401392	0.198948	intron-variant	SPSB1	GRCh38.p7	1:9329403	TGACCTACCCACCAC[C/T]GGGTGTCACCTCCCC	80176
rs926247	snp	A/G	0.4087	0.193169	intron-variant	SPSB1	GRCh38.p7	1:9333949	TACTGGGACAAAAGC[A/G]AAAAAATGAGAAGGA	80176
rs926248	snp	C/T	0.164873	0.23506	intron-variant	SPSB1	GRCh38.p7	1:9317937	TGGCACACAGGGGCC[C/T]TTAACAAACTCGCGG	80176
rs926249	snp	A/G	0.188316	0.242271	intron-variant	SPSB1	GRCh38.p7	1:9317805	GGAAATCACCTACAT[A/G]AGGCTCTGAAACTGT	80176
rs926250	snp	C/T	0.460589	0.13473	intron-variant	SPSB1	GRCh38.p7	1:9314316	TTGTATATTTAGGAG[C/T]GGGAGGGAGGAAGGA	80176
rs1005246	snp	A/G	0.211212	0.246973	intron-variant	SPSB1	GRCh38.p7	1:9364340	CAGCCAGGCCAGACC[A/G]CAGGCTGCGATAAGC	80176
rs1008678	snp	C/T	0.0146672	0.084371	intron-variant	SPSB1	GRCh38.p7	1:9321152	TTTCCAGCTTTGTGT[C/T]TTGGGGGGATTTTTT	80176
rs1008679	snp	C/T	0.208779	0.246578	intron-variant	SPSB1	GRCh38.p7	1:9321027	CCAGCCAGAATCCCC[C/T]GCACAGCAACTCCCA	80176
rs1033377	snp	C/T	0.46137	0.133501	intron-variant	SPSB1	GRCh38.p7	1:9319302	GCACACATGTCCACA[C/T]GCTGACCCGCAGCCC	80176
rs1294020	snp	A/G	0.4087	0.193169	intron-variant	SPSB1	GRCh38.p7	1:9335202	ACAACATTCTTTTGA[A/G]GCACAAAGATACCTT	80176
rs1294021	snp	G/T	0.0236746	0.106192	intron-variant	SPSB1	GRCh38.p7	1:9333929	AATGAGAAGGAATGT[G/T]GCGGAGCATCCCTGG	80176
rs1294022	snp	C/G	0.412416	0.190055	intron-variant	SPSB1	GRCh38.p7	1:9333023	GGGCAGAAGCTCAGT[C/G]AGCACTTGCTGGTGG	80176
rs1294023	snp	C/T	0.329783	0.236927	intron-variant	SPSB1	GRCh38.p7	1:9332029	TCTGTAATTCAAACA[C/T]GTACAAAAGAGTCAC	80176
rs1294024	snp	A/G	0.436408	0.16659	intron-variant	SPSB1	GRCh38.p7	1:9354433	AGAGAGGCCAAGGAG[A/G]GCAGCCTGGTTTGGG	80176
rs1294025	snp	C/T	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9353791	agctgggattacagg[C/T]gcccaccaccacgcc	80176
rs1294027	snp	C/T	0.265453	0.249522	intron-variant	SPSB1	GRCh38.p7	1:9352255	AAGGACGGCTTCACC[C/T]TGACGTGGGACATCC	80176
rs1294028	snp	C/T	0.43555	0.167544	intron-variant	SPSB1	GRCh38.p7	1:9304575	ACTAGTTACCGAAGC[C/T]TACCCATGCCACCTT	80176
rs1294030	snp	A/G	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9301127	cagccaaatcatcag[A/G]cacagcccatggatc	80176
rs1294031	snp	A/G	0.301429	0.244653	intron-variant	SPSB1	GRCh38.p7	1:9301115	caggcacagcccatg[A/G]atcagtatataatca	80176
rs1294032	snp	A/G	0.499741	0.0113788	intron-variant	SPSB1	GRCh38.p7	1:9300377	gcaggttgcacagca[A/G]cctggacctgttgca	80176
rs1294033	snp	C/T	0.0402882	0.136092	intron-variant	SPSB1	GRCh38.p7	1:9300240	caggcccacgaggca[C/T]tgtgcctctttcttg	80176
rs1294034	snp	A/T	0.16911	0.236552	intron-variant	SPSB1	GRCh38.p7	1:9300177	tcaccttagagggga[A/T]accttcacaggcctg	80176
rs1294035	snp	C/T	0.16846	0.236329	intron-variant	SPSB1	GRCh38.p7	1:9300149	ctgacactactggac[C/T]ccgagaaatttcact	80176
rs1294036	snp	A/G	0.163236	0.234461	intron-variant	SPSB1	GRCh38.p7	1:9299628	gctgggtgtggtggc[A/G]catgcctgtaatccc	80176
rs1294037	snp	C/T	0.448708	0.151707	intron-variant	SPSB1	GRCh38.p7	1:9299573	agaattgcttgaacc[C/T]gggaggcggaggttg	80176
rs1294038	snp	A/C	0.078151	0.181571	intron-variant	SPSB1	GRCh38.p7	1:9309146	GCCCACCGACGACCC[A/C]TGGGCCTGGCATTTG	80176
rs1294039	snp	C/T	0.0260105	0.111035	intron-variant	SPSB1	GRCh38.p7	1:9308979	CTGCCAGGGGCTGGG[C/T]GGGCACCAGGCCTGC	80176
rs1294040	snp	C/T	0.45946	0.136478	intron-variant	SPSB1	GRCh38.p7	1:9308150	CCCCTTTGGGCCTGA[C/T]ATGTCTTGGAAAACA	80176
rs1294041	snp	C/T	0.155325	0.23138	intron-variant	SPSB1	GRCh38.p7	1:9307289	accaaatgccactga[C/T]ctgttcactttaaaa	80176
rs1294042	snp	A/G	0.486	0.0824865	intron-variant	SPSB1	GRCh38.p7	1:9306426	CTATAGACAGACCCC[A/G]GTCCATGCACCTCCC	80176
rs1294044	snp	C/T	0.497502	0.035255	intron-variant	SPSB1	GRCh38.p7	1:9306340	GAAAACTGGTTATCC[C/T]TCCCACTCCAGCTCT	80176
rs1294045	snp	G/T	0.459233	0.136827	intron-variant	SPSB1	GRCh38.p7	1:9319682	GGCCGGGCCAGACGA[G/T]CAGGCTTGGCCTCCC	80176
rs1294046	snp	C/T	0.499946	0.00519141	intron-variant	SPSB1	GRCh38.p7	1:9319634	AGCCGGAACGGAATA[C/T]CAGCCCGGTACGGAA	80176
rs1294047	snp	A/G	0.498503	0.0273153	intron-variant	SPSB1	GRCh38.p7	1:9319206	ACCTCCTCTTTTGTT[A/G]TTGTTACTGTTGttt	80176
rs1294048	snp	C/T	0.495671	0.0463237	intron-variant	SPSB1	GRCh38.p7	1:9318913	tgtgagccactgcgc[C/T]cggccCTACCACGTC	80176
rs1294049	snp	C/T	0.499839	0.00898417	intron-variant	SPSB1	GRCh38.p7	1:9318876	ACTCACTGCAGGACA[C/T]CGCAGGCTGGACTCC	80176
rs1294050	snp	G/T	0.471388	0.116136	intron-variant	SPSB1	GRCh38.p7	1:9314417	GGGAAGATGGGCACC[G/T]GGCTGCCCACTTGTG	80176
rs1294051	snp	C/G	0.231111	0.249285	intron-variant	SPSB1	GRCh38.p7	1:9313592	TCTCCCCCAGCAGCC[C/G]GGGCCCACCCCTCCC	80176
rs1294052	snp	A/T	0.481087	0.0953875	intron-variant	SPSB1	GRCh38.p7	1:9313538	CCACCCCAGATCAGG[A/T]GCCTGTTCCCACTCA	80176
rs1294053	snp	G/T	0.499722	0.0117779	intron-variant	SPSB1	GRCh38.p7	1:9310491	TGCCCAGGCTGGTCA[G/T]GAACTCCAGGCCTCA	80176
rs1294054	snp	A/C	0.114036	0.209795	intron-variant	SPSB1	GRCh38.p7	1:9310324	TGAGATGCCTTTCCC[A/C]TCACAGAAATTACCG	80176
rs1294055	snp	G/T	0.184838	0.241358	intron-variant	SPSB1	GRCh38.p7	1:9321975	TAAAACAGACATTGT[G/T]GTTGTCCCCCACAGG	80176
rs1296074	snp	A/C	0.499732	0.0115784	intron-variant	SPSB1	GRCh38.p7	1:9320666	GGTAGGGCAATGTCT[A/C]GAAAATGATCAGAGA	80176
rs1297659	snp	C/T	0.0240643	0.107019	intron-variant	SPSB1	GRCh38.p7	1:9332686	ACAGTATCTGACTCA[C/T]TCTCTAAGGTTCTGT	80176
rs1298553	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9356900	tcattatacacgcat[C/G]catccattattcact	80176
rs1298554	snp	A/G	0	0	intron-variant	SPSB1	GRCh38.p7	1:9321936	TGACTGGAGAGCCCA[A/G]AGCAGGATCACTCGT	80176
rs1299374	snp	C/T	0.265727	0.249505	intron-variant	SPSB1	GRCh38.p7	1:9352349	AGCCTTGTGGGGCTG[C/T]AGCAGGCATTATCCG	80176
rs1299539	snp	C/T	0.0142736	0.0832652	intron-variant	SPSB1	GRCh38.p7	1:9322048	GTGCACATATTTACA[C/T]CACCTGCCCAGTGTG	80176
rs1299906	snp	A/T	0	0	intron-variant	SPSB1	GRCh38.p7	1:9321919	GCAGGATCACTCGTC[A/T]ATGGCACCTACGGGT	80176
rs1339715	snp	A/G	0.498481	0.027514	intron-variant	SPSB1	GRCh38.p7	1:9364999	CGGGACTACAGGCCC[A/G]TGCCACCATGCCTGG	80176
rs1569421	snp	C/G	0.389715	0.207315	intron-variant	SPSB1	GRCh38.p7	1:9327426	TCCCTTTACACCCCA[C/G]AACCTCATTTCCAGC	80176
rs1569422	snp	A/G	0.262435	0.249691	intron-variant	SPSB1	GRCh38.p7	1:9327385	CTGTTTTAGTTATGC[A/G]CTTGCCTGGCGATCG	80176
rs1610407	snp	G/T	0.157972	0.232445	intron-variant	SPSB1	GRCh38.p7	1:9318670	TGTGGCTGGTGCCTC[G/T]GAGGCAGCTGTTTCC	80176
rs1631609	snp	A/T	0.0471551	0.14613	intron-variant	SPSB1	GRCh38.p7	1:9309281	gagagagagagagag[A/T]gtgagagagagtgtg	80176
rs1631612	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9309283	gagagagagagagtg[A/T]gagagagagtgtgtg	80176
rs2012105	snp	G/T	0.36606	0.221428	intron-variant	SPSB1	GRCh38.p7	1:9361136	TGACAGATCCAGCCA[G/T]GCCTGGCCAGAGCCT	80176
rs2018374	snp	A/G	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9304793	cccagctactggggg[A/G]ctgaggtgggaggat	80176
rs2072734	snp	A/G	0.368119	0.220336	intron-variant	SPSB1	GRCh38.p7	1:9296006	TGAAAGTCCAAAATC[A/G]AAGTCCCTTAGAGTC	80176
rs2072735	snp	G/T	0.376592	0.215579	intron-variant	SPSB1	GRCh38.p7	1:9295413	GGGCCAGGTCTCTCT[G/T]AAGCCGGCATGGCAC	80176
rs2075970	snp	A/G	0.380529	0.213219	intron-variant	SPSB1	GRCh38.p7	1:9358774	CCCAGAGCTCATGAC[A/G]GCATCAGGGGGCATG	80176
rs2075971	snp	A/G	0.440471	0.161928	intron-variant	SPSB1	GRCh38.p7	1:9347045	CAGGTGTGAGCCACC[A/G]TGCCCAGCCTGGCAG	80176
rs2075972	snp	A/G	0.43978	0.162738	intron-variant	SPSB1	GRCh38.p7	1:9346920	CGATTATACTGTTTC[A/G]AAATTACAGATTTTA	80176
rs2075973	snp	G/T	0.417265	0.20636	intron-variant	SPSB1	GRCh38.p7	1:9295838	ACCAGCTACAACCTA[G/T]TTCTCGAGAAAAATT	80176
rs2077018	snp	A/G	0.444444	0.157135	intron-variant	SPSB1	GRCh38.p7	1:9361157	AAAAAAAAAAAAAAA[A/G]GAAAATGACAGATCC	80176
rs2105224	snp	A/C	0.210605	0.246877	intron-variant	SPSB1	GRCh38.p7	1:9354684	CTACGATTACAGGCA[A/C]CCACCACCATGCCTG	80176
rs2142574	snp	A/G	0.464629	0.128197	intron-variant	SPSB1	GRCh38.p7	1:9364175	TGTGGCTCAGCCCCC[A/G]CCGGAAAGTGGAGGG	80176
rs2142575	snp	A/G	0.449345	0.150869	intron-variant	SPSB1	GRCh38.p7	1:9364149	GAGGGGCTCTCCCTC[A/G]TGGCTGGAAAGCACC	80176
rs2142577	snp	A/G	0.0142736	0.0832652	intron-variant	SPSB1	GRCh38.p7	1:9298329	TAAGTCTGGGAAGTT[A/G]ATTGAGGGCTGTGAT	80176
rs2205669	snp	C/T	0.367708	0.220556	intron-variant	SPSB1	GRCh38.p7	1:9341223	GTGTGTGTACCGTGC[C/T]TCTCTGTTCTGAGGC	80176
rs2275457	snp	C/T	0.45574	0.142025	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9367810	AAGAGGGGTTGTATA[C/T]GGACGGCATGCAGGG	80176
rs2275458	snp	C/T	0.457037	0.140127	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9367783	AGGGATGCTGCCTTC[C/T]GCTGATGTCGGGAAG	80176
rs2310919	snp	C/T	0.384017	0.211044	intron-variant	SPSB1	GRCh38.p7	1:9355668	ACCCGGAGGGCAAGG[C/T]GACCACATCAGCATG	80176
rs2310920	snp	C/T	0.375	0.216506	intron-variant	SPSB1	GRCh38.p7	1:9354696	CTCCTGCCTCAGCTA[C/T]GATTACAGGCACCCA	80176
rs2310921	snp	C/T	0.490727	0.0674567	intron-variant	SPSB1	GRCh38.p7	1:9328789	GTCAACAGTGCCATG[C/T]TGGGAAGCCCCAGCG	80176
rs2310922	snp	C/T	0.195837	0.244062	intron-variant	SPSB1	GRCh38.p7	1:9317492	TGTCTCAAAAACAAA[C/T]GACAAAAAACCTGTC	80176
rs2310923	snp	A/G	0.436265	0.166749	intron-variant	SPSB1	GRCh38.p7	1:9298838	ggaaccagtgtgtgg[A/G]ttctgccaggtgcta	80176
rs3222159	microsatellite	(CA)25/27/28/29/30	0.592	0.236508	intron-variant	SPSB1	GRCh38.p7	1:9348940	AATACCCCACCACTA[(CA)25/27/28/29/30]ATTCTTGCACGAGTG	80176
rs3765960	snp	A/G	0.383824	0.211166	intron-variant	SPSB1	GRCh38.p7	1:9355533	CACACAGTCGGCCGC[A/G]TGGACAGACAGACCC	80176
rs3795309	snp	A/G	0.378481	0.214459	synonymous-codon	SPSB1	GRCh38.p7	1:9356287	GTGGTTATTCCCCAC[A/G]AGGGTTGTGTACCCG	80176
rs3944982	snp	A/G	0.389903	0.207189	intron-variant	SPSB1	GRCh38.p7	1:9327447	TGTAAAGGGAAGGGG[A/G]TGTCATCGGGGGTCC	80176
rs4071661	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9363754	actcaggctgtagtg[C/G]agtggcgcaatcttg	80176
rs4071662	snp	A/G	0.00795532	0.062565	intron-variant	SPSB1	GRCh38.p7	1:9363761	ctgtagtgcagtggc[A/G]caatcttggctcact	80176
rs4080311	snp	A/T	0.497211	0.037236	intron-variant	SPSB1	GRCh38.p7	1:9295219	CACACACACACACAC[A/T]CTCACACTCTCACAC	80176
rs4271235	snp	A/G	0.439641	0.162899	intron-variant	SPSB1	GRCh38.p7	1:9343943	GGCGCCTGCCACCAC[A/G]CCTGGCTAATTTTTT	80176
rs4319361	snp	A/G	0.436265	0.166749	intron-variant	SPSB1	GRCh38.p7	1:9298805	atttcctggttccag[A/G]ttcaaagttgacata	80176
rs4319362	snp	A/G	0.436265	0.166749	intron-variant	SPSB1	GRCh38.p7	1:9298809	cctggttccagattc[A/G]aagttgacatactta	80176
rs4484947	snp	C/T	0.411074	0.191194	intron-variant	SPSB1	GRCh38.p7	1:9344077	ACAGGCGTGAGCCAC[C/T]GCACCTGGCCAAGAT	80176
rs4908530	snp	C/T	0.499987	0.00259581	intron-variant	SPSB1	GRCh38.p7	1:9318519	CATCCAAGGAAGACC[C/T]TGAGTTTGGAATCTG	80176
rs4908532	snp	C/T	0.499053	0.0217445	intron-variant	SPSB1	GRCh38.p7	1:9329311	GGACAGGTGGACAGG[C/T]GGATGGGTGGACGTG	80176
rs4908533	snp	A/G	0.18	0.24	intron-variant	SPSB1	GRCh38.p7	1:9330475	TGTCTCAAAATAATA[A/G]CAATAATAATAATAA	80176
rs4908536	snp	A/T	0.454784	0.1434	intron-variant	SPSB1	GRCh38.p7	1:9347982	CAGAATCTCGCTCTG[A/T]CGCCCAGGTTCGAGT	80176
rs4908833	snp	C/G	0.421051	0.182323	utr-variant-5-prime	SPSB1	GRCh38.p7	1:9293063	GGCGGCGGCGGCACC[C/G]CGGGCGCGGTAGGCG	80176
rs4908834	snp	G/T	0.469346	0.119947	intron-variant	SPSB1	GRCh38.p7	1:9293105	CTGGGACCCCGATGG[G/T]TGGGCGACCGGCCCG	80176
rs4908835	snp	C/T	0.235854	0.249599	intron-variant	SPSB1	GRCh38.p7	1:9297401	TGACGGGTGCCCCAG[C/T]TGTGAACACACCTTG	80176
rs4908839	snp	A/G	0.0138799	0.0821421	intron-variant	SPSB1	GRCh38.p7	1:9313396	caagagcgaaacacc[A/G]CTCTTCATTTTCTat	80176
rs4908840	snp	C/T	0	0	intron-variant	SPSB1	GRCh38.p7	1:9317349	AGCTTTGATGATACC[C/T]GGTATATAGTAAGTG	80176
rs4908841	snp	C/T	0.470715	0.117409	intron-variant	SPSB1	GRCh38.p7	1:9318466	TGTTCCTCTTTGTCC[C/T]CAAGACCACCCTCCT	80176
rs4908842	snp	C/T	0.484066	0.0878235	intron-variant	SPSB1	GRCh38.p7	1:9327252	TTTTATCTCATCCAG[C/T]TTCATTTCTATTTTT	80176
rs4908843	snp	C/T	0.499104	0.0211472	intron-variant	SPSB1	GRCh38.p7	1:9327300	ATGTATGTAATCTAT[C/T]GATACAGAAGCATGT	80176
rs4908844	snp	C/T	0.487684	0.0775019	intron-variant	SPSB1	GRCh38.p7	1:9330463	GGAGCTAAATTCTGT[C/T]TCAAAATAATAACAA	80176
rs4908845	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9331352	tttttttttttgagg[G/T]ggagtttcactcttg	80176
rs4908846	snp	A/C	0.440333	0.16209	intron-variant	SPSB1	GRCh38.p7	1:9335148	ggcctgtaAAATGCA[A/C]CATTTTGTAAAATGG	80176
rs4908847	snp	C/G	0.489318	0.0722982	intron-variant	SPSB1	GRCh38.p7	1:9335335	ggcgaaaccccgtct[C/G]tactaaaaatacaaa	80176
rs4908851	snp	A/G	0.499295	0.0187567	intron-variant	SPSB1	GRCh38.p7	1:9352728	ACCCTCTGAGGTGTT[A/G]CTCTCCTCGCCTCTT	80176
rs4908852	snp	A/G	0.497091	0.0380279	intron-variant	SPSB1	GRCh38.p7	1:9356903	GAATAATGGATGGAT[A/G]CGTGTATAATGAATT	80176
rs4908853	snp	A/G	0.326035	0.238157	intron-variant	SPSB1	GRCh38.p7	1:9360443	GTATTCGTCTCCTGG[A/G]GCTGCTGAACACATT	80176
rs4908854	snp	C/G	0.392696	0.205275	intron-variant	SPSB1	GRCh38.p7	1:9360482	CAGGACAGCTGAAAA[C/G]AGCAGAAGCGCTCAG	80176
rs4908855	snp	A/G	0.44252	0.159487	intron-variant	SPSB1	GRCh38.p7	1:9360564	TCTGAGGGGGAGCCC[A/G]CCCCATGCCTCCCCT	80176
rs4989532	snp	A/T	0.432504	0.170857	intron-variant	SPSB1	GRCh38.p7	1:9295223	GAGAGTGTGAGTGTG[A/T]GTGTGTGTGTGTGTG	80176
rs5772364	in-del	-/T	0.5	0	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9290959	ATTACCTTTTTTTTC[-/T]TTTTTTTTGAGATGG	80176
rs5772365	in-del	-/GTGT	0.432504	0.170857	intron-variant	SPSB1	GRCh38.p7	1:9295218	TGTGTGAGAGTGTGA[-/GTGT]GTGTGTGTGTGTGTG	80176
rs5772366	in-del	-/T	0.47852	0.101384	intron-variant	SPSB1	GRCh38.p7	1:9330716	CATGTTCTTCTGAAC[-/T]TTTTTTTTTTTAATC	80176
rs5772367	in-del	-/A	0.386504	0.209444	intron-variant	SPSB1	GRCh38.p7	1:9354801	GCAAGACTGCGTCTC[-/A]AAAAAAAAAAGAATT	80176
rs7368328	snp	A/G	0.0126979	0.078662	intron-variant	SPSB1	GRCh38.p7	1:9306536	ccctataggtatcac[A/G]gacattatgacgact	80176
rs9308445	snp	A/T	0.405776	0.195535	intron-variant	SPSB1	GRCh38.p7	1:9324981	GCCTGTGAGCGGGTC[A/T]GTACTGGGTAGGCAG	80176
rs9308446	snp	A/G	0.283158	0.247791	intron-variant	SPSB1	GRCh38.p7	1:9349025	ATTCCTCCCACTGGG[A/G]GAAGAAGTTCACTGA	80176
rs9434757	snp	C/G	0.3746	0.216737	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291726	cacctccagccTCAA[C/G]TGATCTTTTAAATGG	80176
rs9434758	snp	A/G	0.478437	0.10157	intron-variant	SPSB1	GRCh38.p7	1:9307591	CGTCCTGGCTCAGTT[A/G]TAGAGGCCACGTGAA	80176
rs9435202	snp	A/C	0.201418	0.245234	intron-variant	SPSB1	GRCh38.p7	1:9300979	gtggacagctgcagc[A/C]ctatagccccttgct	80176
rs9435206	snp	C/T	0.485324	0.0843964	intron-variant	SPSB1	GRCh38.p7	1:9307624	TGGGATGGAAGAGTC[C/T]GATCCAAACAGCTTG	80176
rs9435207	snp	C/T	0.480539	0.0967035	intron-variant	SPSB1	GRCh38.p7	1:9307650	GCTTGTCTAAGAGGT[C/T]GGCTGGGAAATAGGA	80176
rs9435208	snp	G/T	0.478768	0.100824	intron-variant	SPSB1	GRCh38.p7	1:9307680	AACACCTGTCTTTCT[G/T]TCCATATCCCTCATC	80176
rs9435212	snp	C/T	0.100588	0.200439	intron-variant	SPSB1	GRCh38.p7	1:9309675	cagtgaaaccccgtc[C/T]ctactaaaaatataa	80176
rs9435224	snp	A/G	0.208474	0.246527	intron-variant	SPSB1	GRCh38.p7	1:9321807	CTGGCCAGGGGCACC[A/G]CAGAGACCACGGGAG	80176
rs9435227	snp	C/T	0.320575	0.239832	intron-variant	SPSB1	GRCh38.p7	1:9322081	CCCGAGCACCCATCC[C/T]GCAAGGGGCTTGAAT	80176
rs9435243	snp	A/G	0.396329	0.202701	synonymous-codon	SPSB1	GRCh38.p7	1:9356092	GCTCAATGTCTTTGT[A/G]AAGGAGGACGACAAG	80176
rs9435244	snp	A/G	0.242201	0.249878	intron-variant	SPSB1	GRCh38.p7	1:9357887	TGAGTCCCTTCTACC[A/G]CCTGCAAGTCCCACG	80176
rs9435245	snp	C/T	0.172997	0.237846	intron-variant	SPSB1	GRCh38.p7	1:9359231	TTTAGAGGTTCCAGA[C/T]TGGAAAATAGATGTG	80176
rs9442510	snp	C/T	0.0433465	0.140692	intron-variant	SPSB1	GRCh38.p7	1:9339072	CGGAGCAAGCTCCAC[C/T]GTCTCCAAGGGGAAG	80176
rs9442511	snp	G/T	0.0379877	0.132479	intron-variant	SPSB1	GRCh38.p7	1:9325079	TCTGGAGTCCCAGCT[G/T]CCAGCGAGTGCAGCC	80176
rs9442514	snp	A/C	0.394538	0.203982	intron-variant	SPSB1	GRCh38.p7	1:9295877	AAAATTTTTCAGAAC[A/C]AAAAGATACACTGAG	80176
rs9442531	snp	A/G	0.226188	0.248863	intron-variant	SPSB1	GRCh38.p7	1:9354664	CACCATGCCTGGCTA[A/G]TTTTTGTATTTTTAG	80176
rs9442559	snp	A/T	0.5	0	intron-variant	SPSB1	GRCh38.p7	1:9309335	gagagaatctgtcac[A/T]cacacacacacacac	80176
rs9442562	snp	C/T	0.491051	0.0662916	intron-variant	SPSB1	GRCh38.p7	1:9307849	CCGAAGACCACATCA[C/T]GGATTTACAAATTCA	80176
rs9442568	snp	A/C	0.029116	0.117091	intron-variant	SPSB1	GRCh38.p7	1:9305614	CCTGGCAGTTTAGTT[A/C]CGTGACGGGGAGTCC	80176
rs9442601	snp	A/C	0.445196	0.1562	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9368626	AGCTTCTGAGGATGC[A/C]CTTGGGAAATCTCAG	80176
rs9651158	snp	A/C	0.170733	0.237101	intron-variant	SPSB1	GRCh38.p7	1:9328595	TTCGGGGTAACCCAG[A/C]GGCTGATGAGTGTGT	80176
rs9651297	snp	C/T	0.270621	0.249148	intron-variant	SPSB1	GRCh38.p7	1:9330196	ACAGGCGTGAGCCAC[C/T]GTGCCCAGCCTGGTA	80176
rs9659212	snp	A/G	0.021333	0.101051	intron-variant	SPSB1	GRCh38.p7	1:9349105	TCCCCCTCCTCCAGA[A/G]CTTTTAATGGCCTTC	80176
rs9660159	snp	A/G	0.170733	0.237101	intron-variant	SPSB1	GRCh38.p7	1:9322410	CTCTCATTTTTGCAC[A/G]TTTTCAGCAGATTCT	80176
rs9660182	snp	A/G	0.17332	0.23795	intron-variant	SPSB1	GRCh38.p7	1:9322745	AAGGTGGCAGGTGTC[A/G]GAGAGGGATGTTGAC	80176
rs9660381	snp	A/G	0.0923359	0.194016	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291330	agctgggacttacag[A/G]tgcccgccaccacgc	80176
rs9661380	snp	C/T	0.00557542	0.0525036	intron-variant	SPSB1	GRCh38.p7	1:9348972	gtgtgtgtatatgtg[C/T]gtgtgtgcacgtgca	80176
rs9661847	snp	A/G	0.5	0	intron-variant	SPSB1	GRCh38.p7	1:9298400	agtgaatgaatgaat[A/G]agtgaacgaatgaat	80176
rs9662290	snp	C/T	0.495671	0.0463237	intron-variant	SPSB1	GRCh38.p7	1:9302282	gaatacccaggtaga[C/T]ggtaaagcattgatt	80176
rs9662652	snp	G/T	0.182614	0.240747	intron-variant	SPSB1	GRCh38.p7	1:9341302	CCCAAGGGCATGAGG[G/T]AGGCAGTGGGGGAGA	80176
rs9724706	snp	G/T	0.0209421	0.100162	intron-variant	SPSB1	GRCh38.p7	1:9310430	gggcacagtagctca[G/T]gcctgtaatcccagc	80176
rs9725478	snp	G/T	0.4021	0.198407	intron-variant	SPSB1	GRCh38.p7	1:9324916	CTTGGAAAAGCGAGT[G/T]GGGTGGGGGAGCAGG	80176
rs9725615	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9349901	ACCCATGAGGAGGAC[A/G]GTCCTGCAGTTAGAG	80176
rs9725856	snp	C/G	0.0788843	0.182262	intron-variant	SPSB1	GRCh38.p7	1:9303047	cctggcttctttggg[C/G]tccctgtgcctctgg	80176
rs9725969	snp	A/G	0.268452	0.249318	intron-variant	SPSB1	GRCh38.p7	1:9326325	CTGCGCACTGGAGGT[A/G]GAGACACCCAGGGGC	80176
rs9726425	snp	G/T	0.499325	0.0183582	intron-variant	SPSB1	GRCh38.p7	1:9327431	AAATGAGGTTCTGGG[G/T]TGTAAAGGGAAGGGG	80176
rs9726646	snp	C/T	0.445328	0.156035	intron-variant	SPSB1	GRCh38.p7	1:9315250	TGGGAACCAGCTCAG[C/T]AGATTCCACTGCGAC	80176
rs9727002	snp	G/T	0.093777	0.195178	intron-variant	SPSB1	GRCh38.p7	1:9366650	gtgatctcagcccac[G/T]gcaacctccatctcc	80176
rs9727769	snp	A/T	0.0788843	0.182262	intron-variant	SPSB1	GRCh38.p7	1:9303039	ggctgccacctggct[A/T]ctttgggctccctgt	80176
rs9728078	snp	C/G	0.093777	0.195178	intron-variant	SPSB1	GRCh38.p7	1:9366794	ggccaggctggtctt[C/G]aactcctggcctcaa	80176
rs9728382	snp	C/T	0.0372196	0.131242	intron-variant	SPSB1	GRCh38.p7	1:9319317	ATGTGGACATGTGTG[C/T]GCTGCCCTGGCCGTG	80176
rs9728893	snp	A/G	0.0883596	0.190715	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9368710	ATTCCCCGAGAAGCC[A/G]GGGGCAGGGTGGGAT	80176
rs9728899	snp	A/G	0.0193772	0.0965046	intron-variant	SPSB1	GRCh38.p7	1:9301546	atgtggatagacctg[A/G]gtgcgcacaggacac	80176
rs9729410	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9306924	TTTTACTTttcttct[C/T]ttcttcttttttttt	80176
rs9729583	snp	C/G	0.54295	0.159458	intron-variant	SPSB1	GRCh38.p7	1:9315517	CTCGAGTCACATGAC[C/G]GGGTGGGAGCTGAAT	80176
rs9730431	snp	A/G	0.410061	0.192043	intron-variant	SPSB1	GRCh38.p7	1:9347538	CAAACATAAATAGGC[A/G]CAGAGAGAATCTTTT	80176
rs10157575	snp	A/G	0.0298908	0.118541	intron-variant	SPSB1	GRCh38.p7	1:9326064	TCCCACTCCACCCCT[A/G]CATGTCCCTTAGTTC	80176
rs10159126	snp	G/T	0.440884	0.161442	intron-variant	SPSB1	GRCh38.p7	1:9348226	CTGGGATTACAGGCG[G/T]GAGCCACCGCGGCAA	80176
rs10746488	snp	A/G	0.321769	0.239477	intron-variant	SPSB1	GRCh38.p7	1:9362248	GACCCTATTCCCCAC[A/G]CCCTCCAGAAGTTCT	80176
rs10779719	snp	A/G	0.311859	0.242226	intron-variant	SPSB1	GRCh38.p7	1:9358305	CACGATGTCTGTGGT[A/G]CAGGCTCCCAGGGCT	80176
rs10779720	snp	A/G	0.316243	0.241064	intron-variant	SPSB1	GRCh38.p7	1:9361897	GCAGGCTGTCCAGGG[A/G]GAGCCCCTGACCTTG	80176
rs10864406	snp	A/G	0.223819	0.248625	intron-variant	SPSB1	GRCh38.p7	1:9293872	CGTGTGTGTTTGTGC[A/G]TGTCCTTGTGAATAT	80176
rs10864407	snp	C/T	0.178465	0.239547	intron-variant	SPSB1	GRCh38.p7	1:9316780	TCTGGGTCTGGGGGC[C/T]GCAGCAGCTTCGAGC	80176
rs10864411	snp	C/T	0.472896	0.113214	intron-variant	SPSB1	GRCh38.p7	1:9365481	CTAAGGTCCATTCTT[C/T]TATTTTGTAACAGCT	80176
rs10864412	snp	A/G	0.471863	0.115225	intron-variant	SPSB1	GRCh38.p7	1:9365663	TGCCATGCCCCACCC[A/G]TAGTGTTTGGTCTTC	80176
rs11121361	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9294273	ACACGTGTCTCTGTG[A/T]CTGTCTCTGTGTCTG	80176
rs11121362	snp	C/G	0	0	intron-variant	SPSB1	GRCh38.p7	1:9294274	CACGTGTCTCTGTGT[C/G]TGTCTCTGTGTCTGT	80176
rs11121364	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9296591	AGATGTGCACATGTG[C/T]acacacacatacata	80176
rs11121365	snp	C/G	0.18325	0.240924	intron-variant	SPSB1	GRCh38.p7	1:9297665	GGGTTAAGAAGAGAT[C/G]TGTTTGGTTGGCTGA	80176
rs11121366	snp	A/G	0.172997	0.237846	intron-variant	SPSB1	GRCh38.p7	1:9300229	cctcctgcaaccaag[A/G]aagaggcacaatgcc	80176
rs11121370	snp	C/T	0.179425	0.239831	intron-variant	SPSB1	GRCh38.p7	1:9316760	GCCCCGGAAGCGGCA[C/T]TGGGTCTGGGTCTGG	80176
rs11121371	snp	A/G	0.417359	0.185718	intron-variant	SPSB1	GRCh38.p7	1:9332669	CAGGCGGAGGAGCTG[A/G]GACAGAACCTTAGAG	80176
rs11121372	snp	C/T	0.485392	0.0842056	intron-variant	SPSB1	GRCh38.p7	1:9334140	GCCCAGGCTGGAGTG[C/T]GGTGGTGCGATCTCG	80176
rs11121373	snp	C/T	0.4021	0.198407	intron-variant	SPSB1	GRCh38.p7	1:9336414	TATTTTTAGTAGAGA[C/T]GGGGTTTCTCCACGT	80176
rs11121374	snp	A/G	0.408188	0.193589	intron-variant	SPSB1	GRCh38.p7	1:9336601	CCTCTGCCCGCGTGC[A/G]TTCAAGGAAGAGTCT	80176
rs11121375	snp	C/G	0.485392	0.0842056	intron-variant	SPSB1	GRCh38.p7	1:9336659	TGCCTGAGTTCACCC[C/G]TGGCGCTGGGCTAGT	80176
rs11121376	snp	C/G	0.11228	0.208646	intron-variant	SPSB1	GRCh38.p7	1:9337979	AACGCTCTGGCCAAG[C/G]TCAGCAGCCTGTCTC	80176
rs11121377	snp	A/G	0.466412	0.125164	intron-variant	SPSB1	GRCh38.p7	1:9339841	AGGACAGGGGAAGCT[A/G]CCTGCTCCTTCCGTG	80176
rs11121378	snp	A/C	0.366885	0.220993	intron-variant	SPSB1	GRCh38.p7	1:9343852	GTGCAGTGGCGCGAT[A/C]TCGGCTCACTGAAAG	80176
rs11121379	snp	C/T	0.402982	0.197728	intron-variant	SPSB1	GRCh38.p7	1:9343886	cgcctcctgggttca[C/T]gccattctcctgcct	80176
rs11121380	snp	A/C	0.161924	0.233971	intron-variant	SPSB1	GRCh38.p7	1:9348900	GGGCTTTTGCCGTCA[A/C]AGGATGTAAGGGACA	80176
rs11121381	snp	C/T	0.317451	0.240729	intron-variant	SPSB1	GRCh38.p7	1:9350838	CTTAGGCATCTGCAT[C/T]TGCTTCTCAGAGCAG	80176
rs11121382	snp	C/G	0.305934	0.243663	intron-variant	SPSB1	GRCh38.p7	1:9351410	AGGAAATAAATGAAA[C/G]TGGAAATGCAATAAC	80176
rs11121383	snp	A/G	0.455502	0.142369	intron-variant	SPSB1	GRCh38.p7	1:9353349	CGCAGCTTGAGGCGC[A/G]GGCCCCAAAGCCACA	80176
rs11121384	snp	C/T	0.306927	0.243432	intron-variant	SPSB1	GRCh38.p7	1:9353587	ACACAAGGAGTCCTG[C/T]CCTGCTCTGAAGAGA	80176
rs11121387	snp	C/T	0.101301	0.200969	intron-variant	SPSB1	GRCh38.p7	1:9359263	TCGTTCTTGGGACAC[C/T]GAGCAAAACATTGGA	80176
rs11121388	snp	A/G	0.0607341	0.163335	intron-variant	SPSB1	GRCh38.p7	1:9361589	ACTGGGGCCGTGGCC[A/G]GGCGGAAGTAGGGGT	80176
rs11121389	snp	C/T	0.225597	0.248806	intron-variant	SPSB1	GRCh38.p7	1:9362376	ACAAGGACAAAGGCT[C/T]CACGTTGTGTTTGGC	80176
rs11121390	snp	A/C/G/T	0.182933	0.240836	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9367737	CCTCCATGGGACAAG[A/C/G/T]ACCGATTCCAACACA	80176
rs11577627	snp	A/G	0.401747	0.198678	intron-variant	SPSB1	GRCh38.p7	1:9359614	GGCTGAGGCAGGAGA[A/G]TTGCTTGAACCCGGG	80176
rs11578175	snp	A/C	0.420574	0.182769	intron-variant	SPSB1	GRCh38.p7	1:9339402	AGGACCCAGGGTCCT[A/C]AGGTAATTCCGGGGC	80176
rs11579712	snp	C/G	0.261608	0.24973	intron-variant	SPSB1	GRCh38.p7	1:9347642	ATCGTGTTACATTTT[C/G]TGTTACGTCACCACT	80176
rs11580745	snp	C/T	0.267091	0.249415	intron-variant	SPSB1	GRCh38.p7	1:9349281	CTGCTTCCCCGAGCC[C/T]AGCCCTCCCGTGCAT	80176
rs11581881	snp	C/T	0.335559	0.234904	intron-variant	SPSB1	GRCh38.p7	1:9301517	caaacaaaaaagcaa[C/T]tgggggaagatgtat	80176
rs11582809	snp	A/G	0.4444	0.15719	intron-variant	SPSB1	GRCh38.p7	1:9315952	CACGCGTGCGGCTCC[A/G]GGCATCCTGGTGCAG	80176
rs11582969	snp	G/T	0	0	intron-variant	SPSB1	GRCh38.p7	1:9306021	GGGGTTCGTGCTTTA[G/T]GGAACGAAGGCGTGT	80176
rs11584306	snp	A/T	0.233527	0.249457	intron-variant	SPSB1	GRCh38.p7	1:9321670	AAATAAAAAAAAAAA[A/T]GCTGCTGATTGTCAC	80176
rs11585000	snp	A/G	0.247053	0.249983	intron-variant	SPSB1	GRCh38.p7	1:9320095	AGGGCAGGCCGCCAG[A/G]GACCCCAGGTGTCCA	80176
rs11585098	snp	C/T	0.439224	0.163383	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9292400	GTGGGCACCGAAACG[C/T]GAGCGGCCGAAACAG	80176
rs11585353	snp	C/G	0.0310518	0.120672	intron-variant	SPSB1	GRCh38.p7	1:9325949	CAGGAACAGCCAGAA[C/G]ACCAGTGGGGCAGGC	80176
rs11586656	snp	C/T	0.487368	0.0784625	intron-variant	SPSB1	GRCh38.p7	1:9330906	TCCGGTTTCTCCACA[C/T]CCTTGCCAACACTTG	80176
rs11590191	snp	C/T	0.381503	0.21262	intron-variant	SPSB1	GRCh38.p7	1:9328019	CTGCAATCACACTTA[C/T]GCTTTGGGAGGATTT	80176
rs11591053	snp	A/G	0.35207	0.228214	intron-variant	SPSB1	GRCh38.p7	1:9342571	AAACGTCCCTCTCCC[A/G]CCTCATCCTGCCTTG	80176
rs11591181	snp	A/T	0.240765	0.249829	intron-variant	SPSB1	GRCh38.p7	1:9356688	AACTAGAGTGTTTTG[A/T]AGACGATATTCCAGT	80176
rs11802043	snp	G/T	0.164546	0.234942	intron-variant	SPSB1	GRCh38.p7	1:9294681	GTTCATGGTAAAAGC[G/T]CCATCCCTGGTGACT	80176
rs11805596	snp	A/G	0.00438332	0.0466095	intron-variant	SPSB1	GRCh38.p7	1:9301943	agattcgtcttccct[A/G]cacacagtgcttctg	80176
rs12022674	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9331304	GTTATGGATCTCCTT[C/T]TGCTACTGGTGCTCT	80176
rs12023904	snp	C/G	0	0	intron-variant	SPSB1	GRCh38.p7	1:9342884	CTTCACTCCCCACAT[C/G]TGAGCATCAATGGTG	80176
rs12027268	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9362179	CCACCAGGGCCAccc[A/T]ccctccctccctccc	80176
rs12034435	snp	C/T	0.298144	0.245321	intron-variant	SPSB1	GRCh38.p7	1:9363991	AGGCATAAGCCACCG[C/T]GTCCAGCCTAGAAAC	80176
rs12037734	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9312163	ttattttattttaat[C/T]ttttaattttttaat	80176
rs12044214	snp	C/T	0.459118	0.137002	intron-variant	SPSB1	GRCh38.p7	1:9308994	CGGGCACCAGGCCTG[C/T]GTGGGTACAGAGGGC	80176
rs12044258	snp	A/G	0.413083	0.189483	intron-variant	SPSB1	GRCh38.p7	1:9337494	AGGAAGCCCTCTTTG[A/G]GGGGATGGGAGAACA	80176
rs12045744	snp	A/T	0.296873	0.245566	intron-variant	SPSB1	GRCh38.p7	1:9347195	GCCCTTCTACCAGTT[A/T]TGGATCCTTAACACG	80176
rs12063543	snp	G/T	0.235854	0.249599	intron-variant	SPSB1	GRCh38.p7	1:9365568	tggcctcttgcgtgg[G/T]gagatgtaggaaaca	80176
rs12065293	snp	A/T	0.224116	0.248656	intron-variant	SPSB1	GRCh38.p7	1:9360991	CTGGGGTGCCCATAG[A/T]GAGGTCAGAGCCCAC	80176
rs12069701	snp	C/T	0.197082	0.244335	intron-variant	SPSB1	GRCh38.p7	1:9298949	acatcaaaagcaaca[C/T]tgcatccctggggtg	80176
rs12073748	snp	A/G	0.209084	0.246629	intron-variant	SPSB1	GRCh38.p7	1:9318346	TTGCTTTCTTGGCTG[A/G]CAGTGTAGGACCCTG	80176
rs12074177	snp	A/C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9315668	ATGCAGCCTGGTTTC[A/C/G]ACCCTCTACTAGGGC	80176
rs12077625	snp	C/T	0.167484	0.23599	intron-variant	SPSB1	GRCh38.p7	1:9320187	TTGCATGGCAGAAAC[C/T]TCCTTCTACAGATAT	80176
rs12078305	snp	G/T	0.0452528	0.143452	intron-variant	SPSB1	GRCh38.p7	1:9318218	CCCATGATGCCCCCA[G/T]ATCCTCCACCACGAA	80176
rs12082941	snp	A/G	0.142609	0.225759	intron-variant	SPSB1	GRCh38.p7	1:9335092	tcatatggtaattct[A/G]ttttgagttttttga	80176
rs12087739	snp	A/G	0.141596	0.225274	intron-variant	SPSB1	GRCh38.p7	1:9335489	cctgggtgacagagc[A/G]agtctctgtctcaaa	80176
rs12097920	snp	C/T	0.0134861	0.0810011	intron-variant	SPSB1	GRCh38.p7	1:9334955	atctgtccgtggacg[C/T]gggttgcttgcacct	80176
rs12117701	snp	A/G	0.5	0	intron-variant	SPSB1	GRCh38.p7	1:9348957	TGTGTGTGTGTGTGT[A/G]TATATGTGCGTGTGT	80176
rs12121137	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9295239	gtgtgtgtgtgtgtg[C/T]gtgcgcgcgtgCGGT	80176
rs12124451	snp	C/T	0.00279162	0.0372561	intron-variant	SPSB1	GRCh38.p7	1:9348443	GAGAGAATGGCTGCC[C/T]TAGATCATTAAAGGC	80176
rs12127728	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9304310	tcctggctcccctgg[C/G]tctccagcttgcaga	80176
rs12130640	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9359847	ggccaggatggaagc[C/G]gggggggtgggtggc	80176
rs12132937	snp	C/T			upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291646	gctgctcttgaactc[C/T]tgggcttaagtgatc	80176
rs12136544	snp	A/C	0.172997	0.237846	intron-variant	SPSB1	GRCh38.p7	1:9299955	ggcaacagagtaaga[A/C]cctgtctcaaaaaaa	80176
rs12142657	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9321828	ACCACGGGAGAGGCT[C/T]TTCAGTGGCAGAAGT	80176
rs12145659	snp	C/T	0.210605	0.246877	intron-variant	SPSB1	GRCh38.p7	1:9355207	ACCAGAAGGCCCTTT[C/T]CTGCAGTGAATTGGT	80176
rs12401761	snp	A/C	0.356383	0.226236	intron-variant	SPSB1	GRCh38.p7	1:9362959	CCCAGGCCACAGTGC[A/C]GGTGCCCACCCCCTC	80176
rs12403093	snp	C/T	0.0185938	0.0946107	intron-variant	SPSB1	GRCh38.p7	1:9340809	AAATACCTTTCTCAA[C/T]GCAGCCTGTCTGATG	80176
rs12404134	snp	G/T	0.31721	0.240796	intron-variant	SPSB1	GRCh38.p7	1:9361300	GAGCCACCATGCCCA[G/T]CCGGATCTGTTTTCT	80176
rs12404231	snp	C/T	0.5	0	intron-variant	SPSB1	GRCh38.p7	1:9354245	GGGTTCCTTTGGGTT[C/T]TCTTTGTCTCCTTTA	80176
rs12404367	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9349510	CCTTGGCGCCAGCGC[A/C]GTAGATGCGTGTCAG	80176
rs12562402	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9350558	TGCTCTCACTGTGTA[A/G]GCACACAGTGTACAC	80176
rs12562427	snp	A/G	0.249603	0.25	intron-variant	SPSB1	GRCh38.p7	1:9350821	TGCTGGGCCCCACAA[A/G]GCTTAGGCATCTGCA	80176
rs12562429	snp	A/G	0.375	0.216506	intron-variant	SPSB1	GRCh38.p7	1:9350827	GCCCCACAAGGCTTA[A/G]GCATCTGCATTTGCT	80176
rs12568191	snp	A/G	0.345704	0.230956	intron-variant	SPSB1	GRCh38.p7	1:9338551	CTCGCCCAGGAGGAA[A/G]TATACTTTCTTCTTT	80176
rs12727816	snp	A/G	0.224709	0.248717	intron-variant	SPSB1	GRCh38.p7	1:9354163	GGCCCCATACTGAAG[A/G]GGGAGGCCAGCCCTC	80176
rs12728282	snp	C/T	0.484841	0.0857308	intron-variant	SPSB1	GRCh38.p7	1:9336876	GTCCAGAGACCCAGG[C/T]GGGTACGGGTGAGTT	80176
rs12731339	snp	A/G	0.491316	0.0653198	intron-variant	SPSB1	GRCh38.p7	1:9337170	TGGTCGTTTCCATCT[A/G]GTTGTCCTAGAAACG	80176
rs12734790	snp	A/T	0.457271	0.139781	intron-variant	SPSB1	GRCh38.p7	1:9316470	GTACTCAGCAAGCAG[A/T]GCAGACTTTGATGGG	80176
rs12742286	snp	A/G	0.491051	0.0662916	intron-variant	SPSB1	GRCh38.p7	1:9339136	TGGGGACCCTACTGC[A/G]GGGGCTCCGGAGGTC	80176
rs12743972	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9357000	ggtgggtagggggtg[A/G]atgagtgTTTAGATT	80176
rs12749387	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9348357	CAAACCGTGGCTGTA[A/T]CCAGAAGGCGCTCTC	80176
rs12749844	snp	A/G	0.48995	0.0701706	intron-variant	SPSB1	GRCh38.p7	1:9328212	CTGAGGGAGGAGGCA[A/G]GGCCTGGCCCATCAA	80176
rs12754251	snp	G/T			upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291203	ttttttttttttttg[G/T]gagacggagtctcgc	80176
rs12760778	snp	A/G	0.420255	0.183066	intron-variant	SPSB1	GRCh38.p7	1:9356793	AACGGTGCCTCATGA[A/G]TGAATGGACAGATGG	80176
rs13373777	snp	C/T	0.0298908	0.118541	intron-variant	SPSB1	GRCh38.p7	1:9330602	TAACTTCACCCGACA[C/T]GTTTGGGGGAGTATT	80176
rs17033734	snp	C/G	0.0818113	0.184966	intron-variant	SPSB1	GRCh38.p7	1:9306004	GCGAGTAACGTGGGA[C/G]AGGGGTTCGTGCTTT	80176
rs17377443	snp	C/T	0.110519	0.207473	intron-variant	SPSB1	GRCh38.p7	1:9308077	CAAATCCTGTTAACC[C/T]GTCTGGGACCAGAAC	80176
rs17377597	snp	A/G	0.206642	0.246211	intron-variant	SPSB1	GRCh38.p7	1:9321423	CTGTGTGATTTTACG[A/G]AACTTGTCCTGACCC	80176
rs17377604	snp	C/T	0.223225	0.248562	intron-variant	SPSB1	GRCh38.p7	1:9321445	TCCTGACCCGTTATT[C/T]GTCACCTTGGTGCCC	80176
rs17377611	snp	C/T	0.174932	0.238463	intron-variant	SPSB1	GRCh38.p7	1:9321491	CAGCAGTTCTGTTCT[C/T]CAGACCTTTACCGAA	80176
rs28431239	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9294278	TGTCTCTGTGTCTGT[C/G]TCTGTGTCTGTGTCT	80176
rs28435109	snp	C/T	0.184521	0.241273	intron-variant	SPSB1	GRCh38.p7	1:9342323	ATGAGAAGAGGTTTG[C/T]GTAGTGACAAGTCCA	80176
rs28525009	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9340596	AAACTCCACGCCTGG[C/G]GGGAAGATGGCAGCC	80176
rs28540382	snp	A/G	0.209084	0.246629	intron-variant	SPSB1	GRCh38.p7	1:9319035	ACAAAAAAATTAGCC[A/G]GGCATGGTGGCGCAC	80176
rs28548566	snp	C/T	0.184521	0.241273	intron-variant	SPSB1	GRCh38.p7	1:9342956	CCAGGTCTCTGTAAG[C/T]TCTGTGCCTCTCTCT	80176
rs28552369	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9294310	TGAGTGCGTCTGTGT[A/C]TGTGTGAGTGTCTGT	80176
rs28619204	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9309331	GTGTGTGTGTGTGTG[A/T]GTGAGTGACAGATTC	80176
rs28754287	snp	C/T	0.208779	0.246578	intron-variant	SPSB1	GRCh38.p7	1:9319100	GGAGAATTGCTTGAA[C/T]CTGGGAGGAGGCAGA	80176
rs28790087	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9298895	GGTGGGAAAGGCCAA[A/G]TGGAAACCATTAGCG	80176
rs28873434	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9298856	ACACACTGGTTCCCT[A/G]CCTTGTGCGGTGAGG	80176
rs33924371	in-del	-/T			intron-variant	SPSB1	GRCh38.p7	1:9333348	TTTTTTTTTTTTTTT[-/T]AAGGCAGAGTCTCAC	80176
rs33941706	in-del	-/T	0	0	intron-variant	SPSB1	GRCh38.p7	1:9331291	TCATAAATACCCGTT[-/T]ATGGATCTCCTTCTG	80176
rs33978312	in-del	-/CC	0.00597247	0.0543191	intron-variant	SPSB1	GRCh38.p7	1:9325226	TGCCTCCCACCACCA[-/CC]CCCCCCCCCCGCCCC	80176
rs34018175	in-del	-/C			intron-variant	SPSB1	GRCh38.p7	1:9300956	TATATGAAGGCACAA[-/C]CCCGAAAGTGGACAG	80176
rs34042091	in-del	-/T			frameshift-variant	SPSB1	GRCh38.p7	1:9356419	ATTGTCCCTGACTCC[-/T]TTCCTGGTAGCCCTG	80176
rs34063425	in-del	-/C			intron-variant	SPSB1	GRCh38.p7	1:9325721	CGTCATTGTGAAGTT[-/C]CCATGGGGAAGCTCA	80176
rs34080098	in-del	-/GTT/TGT			intron-variant	SPSB1	GRCh38.p7	1:9364844	TTTTGTTGTTGTTTT[-/GTT/TGT]GTTGTTGTTGTTGTC	80176
rs34108922	in-del	-/T			intron-variant	SPSB1	GRCh38.p7	1:9360344	TTTGGCAACAAGGAA[-/T]TTGGCAGTTGACCTT	80176
rs34148797	in-del	-/TT	0	0	intron-variant	SPSB1	GRCh38.p7	1:9330705	CATGTTCTTCTGAAC[-/TT]TTTTTTTTTTAATCG	80176
rs34172978	in-del	-/A			intron-variant	SPSB1	GRCh38.p7	1:9307337	AACTATCCCCTCTGT[-/A]CTAGTTCCAAACCAT	80176
rs34194438	in-del	-/C			intron-variant	SPSB1	GRCh38.p7	1:9297411	CCAGTTGTGAACACA[-/C]CCTTGCCAGACAGTC	80176
rs34199175	in-del	-/T			intron-variant	SPSB1	GRCh38.p7	1:9331322	TACTGGTGCTCTTGT[-/T]TTTTTTTTTTTTTTT	80176
rs34229353	in-del	-/C			utr-variant-3-prime	SPSB1	GRCh38.p7	1:9368903	TCCCTGGCAACCCCT[-/C]CCACGTAGCGTACCC	80176
rs34229424	in-del	-/T			intron-variant	SPSB1	GRCh38.p7	1:9295300	CTTTACAAGTCTTCC[-/T]TTTTCCAGTCTGGCT	80176
rs34247124	snp	C/T	0.480697	0.0963277	intron-variant	SPSB1	GRCh38.p7	1:9349430	AGGTGAGTGTGGGGT[C/T]AGGGGGCTGTCCCAG	80176
rs34274350	in-del	-/G			intron-variant	SPSB1	GRCh38.p7	1:9351972	CTGCCTGCCCTGCCC[-/G]GGGGAAAACGCCCCA	80176
rs34317170	snp	G/T	0.454544	0.143743	intron-variant	SPSB1	GRCh38.p7	1:9347516	TCTAGACCTTTCTCT[G/T]TACCTACAAACATAA	80176
rs34392416	in-del	-/T			intron-variant	SPSB1	GRCh38.p7	1:9317837	TGGCGAGGGAACCAA[-/T]TTTTTTTTTTTTTTT	80176
rs34481375	in-del	-/A			intron-variant	SPSB1	GRCh38.p7	1:9365664	CCATGCCCCACCCGT[-/A]AGTGTTTGGTCTTCA	80176
rs34507567	in-del	-/T	0.498437	0.0279115	intron-variant	SPSB1	GRCh38.p7	1:9311178	GCGCGGGATAAAGGG[-/T]TTTTTTTTTTTTTTT	80176
rs34548135	in-del	-/G			intron-variant	SPSB1	GRCh38.p7	1:9308233	CTTGCCAGTGCTGTT[-/G]GGGGCAGTGCTGCAG	80176
rs34587915	in-del	-/G			intron-variant	SPSB1	GRCh38.p7	1:9295638	CCAGAGCTGGGGAAT[-/G]GGGGTGGGGGCCTAG	80176
rs34620459	in-del	-/TAA			intron-variant	SPSB1	GRCh38.p7	1:9330479	AATAACAATAATAAT[-/TAA]AATAATAATAAAGAT	80176
rs34661173	in-del	-/G			intron-variant	SPSB1	GRCh38.p7	1:9313407	ACCGCTCTTCATTTT[-/G]CTATAAAATGAAATA	80176
rs34670912	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9364145	CTCAGGTGCTTTCCA[G/T]CCATGAGGGAGAGCC	80176
rs34674229	in-del	-/G			intron-variant	SPSB1	GRCh38.p7	1:9330530	CTCCTACCACCCCAA[-/G]GGGAACCACAGTAAC	80176
rs34708995	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9333294	TTTTCAAGTCCACTT[A/C]TACTTCCTGTCAGTT	80176
rs34710708	in-del	-/T			intron-variant	SPSB1	GRCh38.p7	1:9340869	CACATGAAACGCACA[-/T]TTTGTAGTCCTCCTG	80176
rs34749664	snp	A/G	0.45645	0.140991	intron-variant	SPSB1	GRCh38.p7	1:9319047	GCCGGGCATGGTGGC[A/G]CACCCCTGTAATCCC	80176
rs34765636	in-del	-/G			intron-variant	SPSB1	GRCh38.p7	1:9347075	TTATCCGAGCACTTT[-/G]GGGTGGCCAAGACAG	80176
rs34817952	in-del	-/G	0.253264	0.249979	intron-variant	SPSB1	GRCh38.p7	1:9330558	AACATCCTGCCAGCT[-/G]GACCTTGTGATCTGG	80176
rs34876467	snp	A/C/G/T	0.00364766	0.0425525	synonymous-codon	SPSB1	GRCh38.p7	1:9356200	CGTGTGGCAGATCAC[A/C/G/T]TGGGCCATGAGACAG	80176
rs34942584	in-del	-/T	0.448195	0.152377	intron-variant	SPSB1	GRCh38.p7	1:9340001	CCCCACCGACAGCCC[-/T]TGAACCACCTGGGCA	80176
rs34988310	in-del	-/G			intron-variant	SPSB1	GRCh38.p7	1:9306613	CCTCCCTGCCACCCA[-/G]GGGGAAGAGCTGGGA	80176
rs35048104	in-del	-/C			intron-variant	SPSB1	GRCh38.p7	1:9340114	ATGGTCTGTGGGCCG[-/C]CCTAGGGTCACCGGG	80176
rs35087106	in-del	-/TG			intron-variant	SPSB1	GRCh38.p7	1:9324506	GTCGGCTCGGAGGGC[-/TG]TGGGCCCGGGACTCG	80176
rs35091952	in-del	-/G	0.485324	0.0843964	intron-variant	SPSB1	GRCh38.p7	1:9320968	TCCCCTGCTTAAAAT[-/G]CTCCTTCCCGAGTCC	80176
rs35124523	in-del	-/T	0.418491	0.184691	intron-variant	SPSB1	GRCh38.p7	1:9347419	AAAGGAATACATGCA[-/T]TTTAAAAAATTCAAT	80176
rs35152548	in-del	-/C			intron-variant	SPSB1	GRCh38.p7	1:9366164	GGAAGCGCTCTGTAA[-/C]CCTGGGGCCTGAGGC	80176
rs35154177	in-del	-/T/TT	0.460702	0.134554	intron-variant	SPSB1	GRCh38.p7	1:9317856	GGCGAGGGAACCAAT[-/T/TT]TTTTTTTTTTTTTTT	80176
rs35366582	in-del	-/A	0.495818	0.0455352	intron-variant	SPSB1	GRCh38.p7	1:9353918	TCAAAAAAAAAAAAA[-/A]GGAACCCTGTGTCTC	80176
rs35478739	in-del	-/G			intron-variant	SPSB1	GRCh38.p7	1:9359240	CCAGACTGGAAAATA[-/G]GATGTGGTCGTTCTT	80176
rs35539313	in-del	-/C			intron-variant	SPSB1	GRCh38.p7	1:9341950	CAGGTGATCTGCCCG[-/C]CTCAGGGTCCCAAAG	80176
rs35540239	in-del	-/C			intron-variant	SPSB1	GRCh38.p7	1:9351873	AGATGGCAGAAGTGG[-/C]CCGGGTGTGTGGGCC	80176
rs35670020	in-del	-/C			intron-variant	SPSB1	GRCh38.p7	1:9326770	GTAAGCCCGCTGCTT[-/C]TGAGGGGCCTTCCTC	80176
rs35732316	in-del	-/G			intron-variant	SPSB1	GRCh38.p7	1:9341747	CACTCTTGTTGCCCA[-/G]GCTGGAGTACAATAG	80176
rs35779143	in-del	-/G	0.22263	0.248497	intron-variant	SPSB1	GRCh38.p7	1:9352957	CACAGTTGAGCGGCA[-/G]GGGGGGCTGTGGAGG	80176
rs35820365	in-del	-/C			intron-variant	SPSB1	GRCh38.p7	1:9330650	TTCCTTTCCTCCCCT[-/C]CCTTTTTCTCTCCCT	80176
rs35877709	in-del	-/T	0.5	0	intron-variant	SPSB1	GRCh38.p7	1:9366577	GTGTGTCCTCAGTTC[-/T]TTTTTTTTTTTTTTT	80176
rs35952855	in-del	-/GTGT			intron-variant	SPSB1	GRCh38.p7	1:9309302	AGAGAGAGAGAGAGA[-/GTGT]GTGTGTGTGTGTGTG	80176
rs36013410	in-del	-/G			intron-variant	SPSB1	GRCh38.p7	1:9311632	TTTTTTTATGGGGCA[-/G]GGGGAGCATTCTGTA	80176
rs36047874	in-del	-/A			intron-variant	SPSB1	GRCh38.p7	1:9332189	GACCCCACCTCTACC[-/A]AAAAAAAAAAAAAAA	80176
rs36077602	snp	C/T	0.00874735	0.0655527	intron-variant	SPSB1	GRCh38.p7	1:9359920	ATGGACCGGATGTGA[C/T]GAGAAAGGGAAGCAG	80176
rs36111176	in-del	-/G			intron-variant	SPSB1	GRCh38.p7	1:9349171	GTGTATCCCTCTGCA[-/G]GGGGAAGCCAAGGTG	80176
rs41301983	snp	A/G	0.0655868	0.168795	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9368461	AATCTGGGTGTCTTC[A/G]GGGGCCCGTCTGGAA	80176
rs41526651	snp	A/C	0.0707826	0.174302	intron-variant	SPSB1	GRCh38.p7	1:9344634	CCATAGAATTGCCTA[A/C]TAAAGCTCCAGGCAC	80176
rs55642682	snp	G/T	0.0482946	0.147699	intron-variant	SPSB1	GRCh38.p7	1:9359123	GGGCGCTATTAGTCA[G/T]TGACGAGGATGCTTT	80176
rs55657587	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9347944	CAGTTTCCCTGCAAC[C/T]TTTTTTTTTTTTTTT	80176
rs55669630	snp	C/T	0.093417	0.194889	intron-variant	SPSB1	GRCh38.p7	1:9365253	CCTGGGCCCAACCGA[C/T]CCTCTCGCCTCAGTC	80176
rs55689606	snp	G/T	0.00597247	0.0543191	intron-variant	SPSB1	GRCh38.p7	1:9325238	CCACCCCCCCCCCCC[G/T]CCCCGCCTCCACCGG	80176
rs55707118	snp	A/T	0.338296	0.233889	intron-variant	SPSB1	GRCh38.p7	1:9299718	TCCTGACACCAAGTG[A/T]TTCACCCGCCTTGGC	80176
rs55783493	snp	A/G	0.030665	0.119967	intron-variant	SPSB1	GRCh38.p7	1:9326281	CACCCCAAGGGCTGG[A/G]CAGGTTGCTTTTCTG	80176
rs55796166	snp	C/T	0.0618563	0.164627	intron-variant	SPSB1	GRCh38.p7	1:9330396	CTTGAACCCGGGAGG[C/T]GGAGGTTGCAGTGAG	80176
rs55814907	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9343973	TGTATTTTTAAAAGT[A/G]GAGATGGGGTTTCAC	80176
rs55861239	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9298434	TAAGTGAACGAATGA[A/G]TGAATAAGTGAATGA	80176
rs56045477	snp	C/T	0.188316	0.242271	intron-variant	SPSB1	GRCh38.p7	1:9310141	ATCTGTGATGATGCC[C/T]CTGCACCTGCCGTGG	80176
rs56047985	snp	C/T	0.434976	0.168179	intron-variant	SPSB1	GRCh38.p7	1:9298427	GAATGAATAAGTGAA[C/T]GAATGAATGAATAAG	80176
rs56068827	snp	C/T	0.129664	0.219133	intron-variant	SPSB1	GRCh38.p7	1:9364756	GGCTGTGACCGTCCA[C/T]GGGGGATGAAGAGCA	80176
rs56148717	snp	A/G	0.237593	0.249692	intron-variant	SPSB1	GRCh38.p7	1:9298440	AACGAATGAATGAAT[A/G]AGTGAATGAATAAGT	80176
rs56168702	snp	A/C	0.0185938	0.0946107	intron-variant	SPSB1	GRCh38.p7	1:9342365	CATCAGCCTGGGGCA[A/C]CCCTAGCTGTGGGCA	80176
rs56177980	snp	A/G	0.237593	0.249692	intron-variant	SPSB1	GRCh38.p7	1:9298442	CGAATGAATGAATAA[A/G]TGAATGAATAAGTGA	80176
rs56325526	in-del	-/TAA	0	0	intron-variant	SPSB1	GRCh38.p7	1:9330496	TAATAATAATAATAA[-/TAA]AGATTTGCCAGTCTC	80176
rs56333749	snp	A/C	0.249603	0.25	intron-variant	SPSB1	GRCh38.p7	1:9294461	TTCTGGATAGCCGGG[A/C]ATGCTGGGCCACAGA	80176
rs56373345	snp	A/G	0.499035	0.0219437	intron-variant	SPSB1	GRCh38.p7	1:9348963	TGTGTGTGTGTGTGT[A/G]TATATGTGCGTGTGT	80176
rs56413422	snp	C/G	0.142609	0.225759	intron-variant	SPSB1	GRCh38.p7	1:9326644	TGAGGCTCCTGTGCC[C/G]CGTCCCAGAAAGAAG	80176
rs56655970	in-del	-/T			intron-variant	SPSB1	GRCh38.p7	1:9327267	TTCATTTCTATTTTT[-/T]GGGATGTGTGTTTCA	80176
rs56684759	snp	C/T	0.112983	0.209108	intron-variant	SPSB1	GRCh38.p7	1:9347938	TCTTTGCAGTTTCCC[C/T]GCAACTTTTTTTTTT	80176
rs56691960	snp	A/G	0.489796	0.070696	intron-variant	SPSB1	GRCh38.p7	1:9298386	TGAATGAATGAATGA[A/G]TGAATGAATGAATGA	80176
rs56722751	snp	C/T	0.128976	0.218754	intron-variant	SPSB1	GRCh38.p7	1:9327144	CACTTGCAGCGCTTC[C/T]GGGGGTCCCAGGATG	80176
rs56760449	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9344372	CCACTCCTGTAAAAC[A/C]GGGCCTTTCCATCTG	80176
rs56798022	in-del	-/AAGTGAACGAATGAAT			intron-variant	SPSB1	GRCh38.p7	1:9298420	AACGAATGAATGAAT[-/AAGTGAACGAATGAAT]GAATAAGTGAATGAA	80176
rs56819014	in-del	-/TT			intron-variant	SPSB1	GRCh38.p7	1:9330945	GCGTCTTTTTTTTTT[-/TT]ACATACTTAAAAAAA	80176
rs56835371	snp	A/G	0.00318978	0.0398085	intron-variant	SPSB1	GRCh38.p7	1:9319903	GCAGCCTCCCCGCCT[A/G]TCTAGCCCCAGACCT	80176
rs57156794	snp	C/T	0.209997	0.246779	intron-variant	SPSB1	GRCh38.p7	1:9303032	GGGGTAAGGCTGCCA[C/T]CTGGCTTCTTTGGGC	80176
rs57207160	in-del	-/T	0.402277	0.198272	intron-variant	SPSB1	GRCh38.p7	1:9330936	GTAATTTTCTGCGTC[-/T]TTTTTTTTTACATAC	80176
rs57208644	in-del	-/GAAT			intron-variant	SPSB1	GRCh38.p7	1:9298416	AGTGAACGAATGAAT[-/GAAT]AAGTGAACGAATGAA	80176
rs57284417	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9330705	CATGTTCTTCTGAAC[C/T]TTTTTTTTTTTAATC	80176
rs57286410	snp	C/T	0.5	0	intron-variant	SPSB1	GRCh38.p7	1:9348928	ACATCCCCTTTCACT[C/T]GTGCAAGAATGTGTG	80176
rs57478549	snp	A/C	0.122758	0.215196	intron-variant	SPSB1	GRCh38.p7	1:9300300	TTTGGGTGTGTTACT[A/C]CAGCCCATTTGCTGA	80176
rs57673229	snp	G/T	0.0865458	0.189163	intron-variant	SPSB1	GRCh38.p7	1:9364828	GGTTTTTTTGTTGTT[G/T]TTTTGTTGTTGTTGT	80176
rs57731582	in-del	-/T	0.483563	0.0891524	intron-variant	SPSB1	GRCh38.p7	1:9347963	TTTTTTTTTTTTTTT[-/T]AAACAGAATCTCGCT	80176
rs57798936	snp	A/G	0.0505692	0.150756	intron-variant	SPSB1	GRCh38.p7	1:9362719	GTGGGTTGGGGCTCT[A/G]GGGCTGTGCATGTTC	80176
rs57837536	snp	A/G	0.343924	0.231686	intron-variant	SPSB1	GRCh38.p7	1:9338973	TAATTGTTCCCAGCA[A/G]TGAGGATCGAGTCTG	80176
rs57871457	in-del	-/CTTTTTTTTTTTTCTTTTT			intron-variant	SPSB1	GRCh38.p7	1:9361156	GGATCTGTCATTTTC[-/CTTTTTTTTTTTTCTTTTT]TTTTTTTTTTTTTTT	80176
rs57888220	in-del	-/CCCT	0	0	intron-variant	SPSB1	GRCh38.p7	1:9362195	CCTCCCTCCCTCCCT[-/CCCT]TCCTTCCTTCCTTCC	80176
rs57959755	snp	A/G	0.282105	0.24793	intron-variant	SPSB1	GRCh38.p7	1:9298831	ACATACTTAGCACCT[A/G]GCAGAATCCACACAC	80176
rs57970170	snp	A/T	0.379158	0.214052	intron-variant	SPSB1	GRCh38.p7	1:9343366	GTACAATGTGTGACC[A/T]TTTATATCTGGCTTC	80176
rs57978557	snp	A/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9317571	TGCCTCCCAGGCTCG[A/G]GGATCCTCACACCTC	80176
rs58018233	snp	G/T	0.0858192	0.188533	intron-variant	SPSB1	GRCh38.p7	1:9311634	TTTTTTATGGGGCAG[G/T]GGAGCATTCTGTAGA	80176
rs58056547	snp	C/T	0.121717	0.214577	intron-variant	SPSB1	GRCh38.p7	1:9332230	GCGTTTTAGGAAGAT[C/T]TGTTTGAGTGGGCTG	80176
rs58085873	in-del	-/GTGAATGAATGA			intron-variant	SPSB1	GRCh38.p7	1:9298386	TGAATGAATGAATGA[-/GTGAATGAATGA]ATGAGTGAACGAATG	80176
rs58099509	in-del	-/A	0.421842	0.181577	intron-variant	SPSB1	GRCh38.p7	1:9335898	TACCCTCCGAATGTC[-/A]ATGTGCACAGTAGTA	80176
rs58102922	snp	C/G	0.379158	0.214052	intron-variant	SPSB1	GRCh38.p7	1:9343365	CGTACAATGTGTGAC[C/G]TTTTATATCTGGCTT	80176
rs58198864	in-del	-/AGTG/AGTT	0	0	intron-variant	SPSB1	GRCh38.p7	1:9294272	ACACGTGTCTCTGTG[-/AGTG/AGTT]TCTGTCTCTGTGTCT	80176
rs58250473	snp	C/G	0.128976	0.218754	intron-variant	SPSB1	GRCh38.p7	1:9328369	GTTCAGCAGAACCTT[C/G]CGTTTCTGTCCTGCG	80176
rs58276325	in-del	-/A/AA	0	0	intron-variant	SPSB1	GRCh38.p7	1:9314182	CTCAAAAAAAAAAAA[-/A/AA]CAAAAAACAAAAAAA	80176
rs58312138	snp	A/C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9349060	AAACCCCAGGGCTTC[A/C/G]TGTCATCTGGTGTCC	80176
rs58335829	snp	C/T	0.00597247	0.0543191	intron-variant	SPSB1	GRCh38.p7	1:9325224	AATGCCTCCCACCAC[C/T]ACCCCCCCCCCCCGC	80176
rs58367040	in-del	-/T			intron-variant	SPSB1	GRCh38.p7	1:9361183	TTTTTTTTTTTTTTT[-/T]AGAGATGGGGTCTCA	80176
rs58412622	snp	G/T	0.0744748	0.178019	intron-variant	SPSB1	GRCh38.p7	1:9335066	GAACACCCAGAAGTG[G/T]ATTTTCTAGGTCATA	80176
rs58438510	in-del	-/GTCT			intron-variant	SPSB1	GRCh38.p7	1:9294176	TGTCTCTGAGTGTCT[-/GTCT]CTGCAAATGTGTGTC	80176
rs58753184	snp	A/G	0	0	intron-variant	SPSB1	GRCh38.p7	1:9298390	TGAATGAATGAGTGA[A/G]TGAATGAATGAGTGA	80176
rs58793866	in-del	-/AGAT	0.081446	0.184634	intron-variant	SPSB1	GRCh38.p7	1:9356962	AGTGGTTGAACAAAC[-/AGAT]GGATGGATGTGGGTG	80176
rs58811152	in-del	-/GTGAG			intron-variant	SPSB1	GRCh38.p7	1:9365567	GTGGCCTCTTGCGTG[-/GTGAG]ATGTAGGAAACAATT	80176
rs58852106	in-del	-/GTGAATGA			intron-variant	SPSB1	GRCh38.p7	1:9298386	TGAATGAATGAATGA[-/GTGAATGA]ATGAATGAGTGAACG	80176
rs58976108	snp	A/C	0	0	intron-variant	SPSB1	GRCh38.p7	1:9325228	CCTCCCACCACCACC[A/C]CCCCCCCCCGCCCCG	80176
rs59017869	snp	G/T	0.0858192	0.188533	intron-variant	SPSB1	GRCh38.p7	1:9364830	TTTTTTTGTTGTTGT[G/T]TTGTTGTTGTTGTTG	80176
rs59100551	snp	C/T	0.0441095	0.141807	intron-variant	SPSB1	GRCh38.p7	1:9316980	GGCCCCGTAGCAGGG[C/T]CAGGCCTCACCTTGG	80176
rs59126337	snp	A/G	0.0551013	0.156571	intron-variant	SPSB1	GRCh38.p7	1:9357247	GATGGATGGATAAAT[A/G]AACAGGTGGATGAGT	80176
rs59423584	snp	C/T	0.0763149	0.179815	intron-variant	SPSB1	GRCh38.p7	1:9362546	CATGACAGCTGTCAG[C/T]GAGGACATTGCGGAA	80176
rs59436212	in-del	-/TT			intron-variant	SPSB1	GRCh38.p7	1:9311177	TTTTTTTTTTTTTTT[-/TT]AATGCCTTCATCATG	80176
rs59441316	in-del	-/T/TT			intron-variant	SPSB1	GRCh38.p7	1:9366593	TTTTTTTTTTTTTTT[-/T/TT]GGACCGAGTCTTGCT	80176
rs59559927	in-del	-/AGTG			intron-variant	SPSB1	GRCh38.p7	1:9294106	CTGTGTGTCTTTGTG[-/AGTG]TGTGTCTGTGTGTGA	80176
rs59580822	in-del	-/AAA			intron-variant	SPSB1	GRCh38.p7	1:9343968	TTTTTTGTATTTTTA[-/AAA]GTAGAGATGGGGTTT	80176
rs59721093	in-del	-/GT			intron-variant	SPSB1	GRCh38.p7	1:9331173	TTTTAATTGCTGTGT[-/GT]AACAACGGTTCATGG	80176
rs59753850	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9341052	GATTGCTGGCCTGGA[A/C]TAGCCCATTCAATGG	80176
rs60016245	in-del	-/GT			intron-variant	SPSB1	GRCh38.p7	1:9294046	TGTGTGTGTGTGTGT[-/GT]CTGAGTGCGTCTTTG	80176
rs60075478	in-del	-/CG			intron-variant	SPSB1	GRCh38.p7	1:9325237	ACCACCCCCCCCCCC[-/CG]CCCCGCCTCCACCGG	80176
rs60111082	snp	G/T	0.368938	0.219895	intron-variant	SPSB1	GRCh38.p7	1:9331524	TTTAGTAGAAACGGG[G/T]TTTCATCATGTTGAC	80176
rs60234846	snp	C/G	0.487558	0.0778863	intron-variant	SPSB1	GRCh38.p7	1:9337819	CTGTCTCTCCTGGGA[C/G]GCCCCATGAAGCCAG	80176
rs60355243	in-del	-/CCC/CCT			intron-variant	SPSB1	GRCh38.p7	1:9301544	TATGTGGATAGACCT[-/CCC/CCT]GAGTGCGCACAGGAC	80176
rs60402136	snp	A/C	0.261884	0.249717	intron-variant	SPSB1	GRCh38.p7	1:9348224	TGCTGGGATTACAGG[A/C]GTGAGCCACCGCGGC	80176
rs60444586	snp	C/T	0.0482946	0.147699	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9368468	GTGTCTTCGGGGGCC[C/T]GTCTGGAAGGGCTGC	80176
rs60472004	snp	C/T	0.0322114	0.122752	intron-variant	SPSB1	GRCh38.p7	1:9365763	TAGGATGGAGTTTTG[C/T]GGGTTCCTTTTAGTT	80176
rs60674790	snp	C/T	0.434976	0.168179	intron-variant	SPSB1	GRCh38.p7	1:9298407	GAATGAATGAGTGAA[C/T]GAATGAATGAATAAG	80176
rs61011475	in-del	-/CC			intron-variant	SPSB1	GRCh38.p7	1:9325236	CACCACCCCCCCCCC[-/CC]GCCCCGCCTCCACCG	80176
rs61039900	snp	C/T	0.0584853	0.160693	intron-variant	SPSB1	GRCh38.p7	1:9366065	TCATCTGAGATGCAG[C/T]TGAATGAACTCAGCC	80176
rs61161076	snp	C/T	0.0422008	0.138995	intron-variant	SPSB1	GRCh38.p7	1:9343210	CCCCTAAAAGAGGCT[C/T]GAGTCCCAAAACAGT	80176
rs61388173	snp	G/T	0.284471	0.247612	intron-variant	SPSB1	GRCh38.p7	1:9352551	CAGGCATTTACTATC[G/T]CGCCCATTTCAGAAA	80176
rs61484781	snp	C/T	0.188316	0.242271	intron-variant	SPSB1	GRCh38.p7	1:9310140	CATCTGTGATGATGC[C/T]TCTGCACCTGCCGTG	80176
rs61620058	in-del	-/A	0	0	intron-variant	SPSB1	GRCh38.p7	1:9335515	TCAAAAAAAAAAAAA[-/A]GATCGTTGTGGGGTC	80176
rs61681348	snp	C/T	0.00636936	0.0560724	intron-variant	SPSB1	GRCh38.p7	1:9343934	GGGACTAGAGGCGCC[C/T]GCCACCACGCCTGGC	80176
rs61783470	snp	A/G	0.180064	0.240019	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291432	CCTCGTGATCCGCCC[A/G]CCTCGACCTCCCAAA	80176
rs61783472	snp	C/T	0.24932	0.249999	intron-variant	SPSB1	GRCh38.p7	1:9294986	GGCGGTTCACTTACC[C/T]AGACTGCACAGCCAG	80176
rs61783473	snp	A/T	0.273856	0.248859	intron-variant	SPSB1	GRCh38.p7	1:9295209	GTGTGTGTGTGTGTG[A/T]GAGTGTGAGTGTGTG	80176
rs61783474	snp	A/T	0.5	0	intron-variant	SPSB1	GRCh38.p7	1:9295211	GTGTGTGTGTGTGAG[A/T]GTGTGAGTGTGTGTG	80176
rs61783475	snp	A/T	0.304438	0.244001	intron-variant	SPSB1	GRCh38.p7	1:9295217	GTGTGTGAGAGTGTG[A/T]GTGTGTGTGTGTGTG	80176
rs61783484	snp	A/G	0.5	0	intron-variant	SPSB1	GRCh38.p7	1:9298394	TGAATGAGTGAATGA[A/G]TGAATGAGTGAACGA	80176
rs61783485	snp	A/G	0.5	0	intron-variant	SPSB1	GRCh38.p7	1:9298402	TGAATGAATGAATGA[A/G]TGAACGAATGAATGA	80176
rs61783487	snp	A/G	0.5	0	intron-variant	SPSB1	GRCh38.p7	1:9298412	AATGAGTGAACGAAT[A/G]AATGAATAAGTGAAC	80176
rs61783488	snp	A/G	0.5	0	intron-variant	SPSB1	GRCh38.p7	1:9298414	TGAGTGAACGAATGA[A/G]TGAATAAGTGAACGA	80176
rs61783489	snp	A/G	0	0	intron-variant	SPSB1	GRCh38.p7	1:9298422	CGAATGAATGAATAA[A/G]TGAACGAATGAATGA	80176
rs61783491	snp	G/T	0.281049	0.248064	intron-variant	SPSB1	GRCh38.p7	1:9299742	CCTTGGCCTCCCAAA[G/T]TTCTGGGATTACAGG	80176
rs61783492	snp	C/T	0.453453	0.145282	intron-variant	SPSB1	GRCh38.p7	1:9300136	GACCTTCTCCCTTAG[C/T]GAAATTTCTCGGGGT	80176
rs61783493	snp	C/T	0.0107246	0.0724382	intron-variant	SPSB1	GRCh38.p7	1:9308501	CCTTGTTGGAGCTCC[C/T]GACAACTTGTTCCTG	80176
rs61783513	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9347966	TTTTTTTTTTTTTAA[A/T]CAGAATCTCGCTCTG	80176
rs61783514	snp	C/T	0.5	0	intron-variant	SPSB1	GRCh38.p7	1:9347967	TTTTTTTTTTTTAAA[C/T]AGAATCTCGCTCTGA	80176
rs61783549	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9363700	CCTCTGCAGTTTTAG[A/T]AAATTTTTTTTTTTT	80176
rs67551275	snp	C/T	0.466308	0.125343	intron-variant	SPSB1	GRCh38.p7	1:9296617	ACATATGCACACACA[C/T]ATATGCACACATACA	80176
rs70979728	in-del	-/TGTG	0	0	intron-variant	SPSB1	GRCh38.p7	1:9295239	GTGTGTGTGTGTGTG[-/TGTG]CGCGCGTGCGGTTGG	80176
rs70979729	in-del	-/TTCTT	0	0	intron-variant	SPSB1	GRCh38.p7	1:9306920	TTTACTTTTCTTCTT[-/TTCTT]CTTTTTTTTTTTTTT	80176
rs70979731	in-del	-/AGTTCAAGACCAG/GAGTTCAAGACCA	0	0	intron-variant	SPSB1	GRCh38.p7	1:9318982	TCACCTGAGGTCATG[-/AGTTCAAGACCAG/GAGTTCAAGACCA]CCTGGGCAACATGGC	80176
rs70979734	in-del	-/AA	0	0	intron-variant	SPSB1	GRCh38.p7	1:9359721	AAAAAAAAAAAAAAA[-/AA]GTATCATTCTGGCTG	80176
rs71580080	in-del	-/A	0.5	0	intron-variant	SPSB1	GRCh38.p7	1:9309812	CACCATTGCACTCCA[-/A]GCCTGGGCAATAGTG	80176
rs71580081	in-del	-/CC	0.5	0	intron-variant	SPSB1	GRCh38.p7	1:9331625	GTGAGTCACCGTGCC[-/CC]TAGCCGGCACTCATT	80176
rs71580082	in-del	-/T	0.225597	0.248806	intron-variant	SPSB1	GRCh38.p7	1:9343796	GTTTTTTATTTTTTT[-/T]GAGACAGAGTCTCGC	80176
rs71580083	in-del	-/AA/AAA/GAAAAAAA	0.00318978	0.0398085	intron-variant	SPSB1	GRCh38.p7	1:9359705	GACTCCGTCTCTGGG[-/AA/AAA/GAAAAAAA]AAAAAAAAAAAAAAA	80176
rs71580084	in-del	-/A/G	0.315273	0.241329	intron-variant	SPSB1	GRCh38.p7	1:9359847	GCCAGGATGGAAGCC[-/A/G]GGGGGGGTGGGTGGC	80176
rs71641086	snp	C/T	0.5	0	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291296	GTTCACACCATTCTC[C/T]TGCCTCAGCCTCCCA	80176
rs71641087	snp	A/G	0.5	0	intron-variant	SPSB1	GRCh38.p7	1:9318032	GCCAGGTGGGGAGAG[A/G]AAGCAGCTGCGCTCA	80176
rs71641088	snp	C/G/T	0.00279162	0.0372561	intron-variant	SPSB1	GRCh38.p7	1:9320127	GCGTCTGCTTCTCAC[C/G/T]GGCCCCACCCCCCAC	80176
rs71641089	snp	A/G	0.5	0	intron-variant	SPSB1	GRCh38.p7	1:9360780	TGAAGTACATCCGCA[A/G]GGCCCTGTTTCCAGA	80176
rs71641090	snp	A/G	0.254944	0.249951	intron-variant	SPSB1	GRCh38.p7	1:9361476	CAGCAGTTTGCCTGC[A/G]TGTGTGCCTTCCCGG	80176
rs72470184	snp	A/G	0.00279162	0.0372561	intron-variant	SPSB1	GRCh38.p7	1:9304048	TCTGCCCTCCATGGG[A/G]TCAGCCACCGTCCAA	80176
rs72642709	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9295243	GTGTGTGTGTGTGTG[C/T]GCGCGTGCGGTTGGG	80176
rs72642711	snp	A/C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9297968	CCTTACAGTGGGAGC[A/C/T]GCAGTCACTCAAATG	80176
rs72642725	snp	C/T	0.0298908	0.118541	intron-variant	SPSB1	GRCh38.p7	1:9311499	TCTCTTCACCATGCA[C/T]GGGACATCTTCTTTT	80176
rs72642726	snp	G/T	0.0298908	0.118541	intron-variant	SPSB1	GRCh38.p7	1:9311508	CATGCATGGGACATC[G/T]TCTTTTCTGGAAAGA	80176
rs72642729	snp	C/T	0.0279526	0.114869	intron-variant	SPSB1	GRCh38.p7	1:9314827	AACTCACATGCCCCC[C/T]GGGGTCAGGAAGGAG	80176
rs72642735	snp	C/G	0.0644693	0.167566	intron-variant	SPSB1	GRCh38.p7	1:9316935	TAGAGGGAGCTGCCT[C/G]GTGCTCTCCTTCTGA	80176
rs72642736	snp	G/T	0.0279526	0.114869	intron-variant	SPSB1	GRCh38.p7	1:9317082	GCTTCCGGTGCTCTC[G/T]CGAAGGAAAGAGAGA	80176
rs72642738	snp	G/T	0.438105	0.164671	intron-variant	SPSB1	GRCh38.p7	1:9317467	ATTTTCAGACCACCA[G/T]GTGAGAACAGACAGG	80176
rs72642739	snp	C/G	0.0584853	0.160693	intron-variant	SPSB1	GRCh38.p7	1:9318240	CACCACGAATGCAGC[C/G]GGCAGCAGAACAGTG	80176
rs72642747	snp	C/T	0.0279526	0.114869	intron-variant	SPSB1	GRCh38.p7	1:9320256	CAGGGGGTTGCAGCT[C/T]GACCAAGACAGACTG	80176
rs72642750	snp	A/G	0.031825	0.122064	intron-variant	SPSB1	GRCh38.p7	1:9322786	GGTCTTGTTCTGGCC[A/G]GTCTGATGGTCAGCG	80176
rs72643817	snp	A/T	0.0267878	0.112589	intron-variant	SPSB1	GRCh38.p7	1:9330788	GCAGTTCAGTAGCGT[A/T]GAGTACATTACCGGA	80176
rs72643823	snp	C/T	0.0314385	0.121371	intron-variant	SPSB1	GRCh38.p7	1:9336524	AGCCACCACGTCCGG[C/T]TCCTCCTCCTGGTTC	80176
rs72643827	snp	C/G	0.031825	0.122064	intron-variant	SPSB1	GRCh38.p7	1:9337806	CCTCACTCTGTCTCT[C/G]TCTCTCCTGGGACGC	80176
rs72643829	snp	A/G	0.0279526	0.114869	intron-variant	SPSB1	GRCh38.p7	1:9338533	TCTCTTGCCAGCTCC[A/G]GCCTCGCCCAGGAGG	80176
rs72643830	snp	C/T	0.323434	0.238972	intron-variant	SPSB1	GRCh38.p7	1:9338560	GAGGAAGTATACTTT[C/T]TTCTTTGCTGGTGAG	80176
rs72643833	snp	G/T	0.0581099	0.160244	intron-variant	SPSB1	GRCh38.p7	1:9338929	GGCCCCATTCTGGAG[G/T]ACTCTGGAAAACCCG	80176
rs72643837	snp	C/T	0.02016	0.0983543	intron-variant	SPSB1	GRCh38.p7	1:9339777	TCTGGGCAAGGGGAT[C/T]GGCAGCCTGTTTATG	80176
rs72643839	snp	A/G	0.0329836	0.124112	intron-variant	SPSB1	GRCh38.p7	1:9340129	CCCTAGGGTCACCGG[A/G]TGCAGGGCACGCAGG	80176
rs72643842	snp	C/T	0.0182019	0.0936463	intron-variant	SPSB1	GRCh38.p7	1:9343633	ACATTTTCATTTCTC[C/T]GGGCTCCTTTCTACC	80176
rs72643850	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9357512	TACTAGGGCCTCTCC[A/G]GTAAATGAATGCTAG	80176
rs72858135	snp	C/T	0.0652144	0.168387	intron-variant	SPSB1	GRCh38.p7	1:9294538	CTCTTCCTCTCTCCA[C/T]TTCTCTGAAAATGAA	80176
rs72858142	snp	A/G	0.0456336	0.143994	intron-variant	SPSB1	GRCh38.p7	1:9295657	GTGGGGGCCTAGCCC[A/G]TGGAAGCCAGCGCTG	80176
rs72858166	snp	A/C	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9315628	CCTTGGCCTGATGCC[A/C]GTGACCTTGCCCTCC	80176
rs72858167	snp	A/G	0.0166325	0.0896639	intron-variant	SPSB1	GRCh38.p7	1:9316156	CCTTGCCCTGGGCTG[A/G]CAGGGGGTGGGGACC	80176
rs72858170	snp	C/T	0.154993	0.231244	intron-variant	SPSB1	GRCh38.p7	1:9316876	GTGACCTCTCTGAGC[C/T]TCAGTTTCCATCTGT	80176
rs72860834	snp	C/T	0.0134861	0.0810011	intron-variant	SPSB1	GRCh38.p7	1:9318628	CTTACCTTGCGGAAT[C/T]GTGCAGGATTGACCA	80176
rs72860840	snp	G/T	0.164546	0.234942	intron-variant	SPSB1	GRCh38.p7	1:9319251	GGGGGGACCAGGGGG[G/T]TGGCACAGGGAGGGC	80176
rs72860844	snp	C/T	0.190205	0.242744	intron-variant	SPSB1	GRCh38.p7	1:9319607	GCATGCTGTGTCTCA[C/T]GGTGGCTGATGTTCC	80176
rs72860847	snp	A/G	0.0372196	0.131242	intron-variant	SPSB1	GRCh38.p7	1:9320349	TCCTCCATCCCAGCC[A/G]GATGGCTGAAAGCTC	80176
rs72860849	snp	A/C	0.0134861	0.0810011	intron-variant	SPSB1	GRCh38.p7	1:9325016	ATTGGGAGCCACAGC[A/C]ACTCACTGGCTGCTG	80176
rs72860850	snp	A/G	0.0130921	0.0798413	intron-variant	SPSB1	GRCh38.p7	1:9325068	GTGGATGCAGTGGCT[A/G]CACTCGCTGGAAGCT	80176
rs72860851	snp	C/T	0.0154538	0.0865337	intron-variant	SPSB1	GRCh38.p7	1:9328534	TTTCTTTCAATGCTT[C/T]GTTTTATAAACAGGG	80176
rs72860855	snp	A/G	0.155325	0.23138	intron-variant	SPSB1	GRCh38.p7	1:9331807	AGCAATCTGGAGGGT[A/G]CAACGTGCGATCTCA	80176
rs72860869	snp	G/T	0.225597	0.248806	intron-variant	SPSB1	GRCh38.p7	1:9344308	TTTGCATCTCTGAGT[G/T]CCCAGGTGACGCTGA	80176
rs72860876	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9351851	ATTGACCACCTGGGA[A/G]GTGACTCAGATGGCA	80176
rs74051607	snp	A/G	0.00795532	0.062565	intron-variant	SPSB1	GRCh38.p7	1:9309030	GAGACTGTCAGGAGG[A/G]TTTGTTCTAGGCTGG	80176
rs74051610	snp	A/C/G/T	0.00954224	0.0684493	intron-variant	SPSB1	GRCh38.p7	1:9316558	CTGGATGGCGAGGAG[A/C/G/T]GGGGGGCTGATCGAA	80176
rs74051617	snp	A/G	0.5	0	intron-variant	SPSB1	GRCh38.p7	1:9318912	AGACGTGGTAGGGCC[A/G]GGCGCAGTGGCTCAC	80176
rs74051620	snp	A/G	0.235564	0.249583	intron-variant	SPSB1	GRCh38.p7	1:9319685	AGGCCAAGCCTGCTC[A/G]TCTGGCCCGGCCAGA	80176
rs74051621	snp	A/G	0.0383715	0.133092	intron-variant	SPSB1	GRCh38.p7	1:9319777	TCGGCCTGGGGTGGC[A/G]GGGTGACTGGTTCCA	80176
rs74051624	snp	G/T	0.162909	0.23434	intron-variant	SPSB1	GRCh38.p7	1:9329096	TGTGTAGGAGTTCGC[G/T]TGGGGGACAGGGTGG	80176
rs74051625	snp	C/T	0.123798	0.215808	intron-variant	SPSB1	GRCh38.p7	1:9330893	GATACCCAAGGGTTC[C/T]GGTTTCTCCACATCC	80176
rs74051628	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9332279	GACTCTTGCAGTGGC[C/G]TTGCAAGTGATGACT	80176
rs74051629	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9338562	GGAAGTATACTTTCT[G/T]CTTTGCTGGTGAGTT	80176
rs74051630	snp	C/T	0.0275645	0.114116	intron-variant	SPSB1	GRCh38.p7	1:9341498	AATGAATTCCAGCCC[C/T]GAGGCACATTATTTG	80176
rs74051631	snp	C/T	0.0944967	0.195752	intron-variant	SPSB1	GRCh38.p7	1:9345019	ATGTCCAAGAGACTG[C/T]CTTGTTGGGGGAAAG	80176
rs74051635	snp	A/G	0.0333695	0.124785	intron-variant	SPSB1	GRCh38.p7	1:9348896	TTGAGGGCTTTTGCC[A/G]TCAAAGGATGTAAGG	80176
rs74051637	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9350475	GAATGGAGAGCAGGC[A/G]CCGCCGGCCAGGGCA	80176
rs74051642	snp	C/T	0.0178098	0.0926698	intron-variant	SPSB1	GRCh38.p7	1:9366356	AGAAGCACAGACACC[C/T]GGGGTTTCTCTGTCT	80176
rs74312763	in-del	-/C			intron-variant	SPSB1	GRCh38.p7	1:9309229	GTGCAGATAAGCTAG[-/C]AYYCCCCCTCAATTC	80176
rs74449281	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9347422	GGAATACATGCATTT[A/T]AAAAAATTCAATTCA	80176
rs74477721	in-del	-/C	0	0	intron-variant	SPSB1	GRCh38.p7	1:9309230	TGCAGATAAGCTAGA[-/C]TCCCCCCTCAATTCC	80176
rs74523864	snp	A/G	0.0228947	0.104514	intron-variant	SPSB1	GRCh38.p7	1:9356668	GCCAAAAGTTGATTC[A/G]TTGGAACTAGAGTGT	80176
rs74526239	snp	C/T	0.046775	0.145601	intron-variant	SPSB1	GRCh38.p7	1:9326782	CTTCTGAGGGGCCTT[C/T]CTCATTCCTGCAGTT	80176
rs74613047	snp	G/T	0.0618563	0.164627	intron-variant	SPSB1	GRCh38.p7	1:9301302	TCGAGACCAGCCTGA[G/T]CAACATAGTGAGACT	80176
rs74619104	snp	C/T	0.0741063	0.177655	intron-variant	SPSB1	GRCh38.p7	1:9349311	TGAGACAGACGCTCC[C/T]GCCACGTGCTCGACT	80176
rs74634905	snp	A/G	0.046775	0.145601	intron-variant	SPSB1	GRCh38.p7	1:9363196	GTTAGACCGGGCCCT[A/G]TGCGCCATCAGTTTC	80176
rs74765885	snp	C/T	0.0437281	0.141251	intron-variant	SPSB1	GRCh38.p7	1:9345044	GGAAAGTGGCAGACT[C/T]TGGATGCACTCCAGC	80176
rs74768091	snp	C/T	0.00358779	0.0422022	intron-variant	SPSB1	GRCh38.p7	1:9366515	CAGGCTGCCTGGATT[C/T]AGATCCCAGCCCTGA	80176
rs74832003	snp	A/G	0.0193772	0.0965046	intron-variant	SPSB1	GRCh38.p7	1:9300082	TGGTAGGACATTTAC[A/G]TGTCAAGCGATGGGA	80176
rs74868326	snp	A/G	0.5	0	intron-variant	SPSB1	GRCh38.p7	1:9329721	AAAAAAAAAAAAAAA[A/G]AGAGAAAAGAAAGAA	80176
rs74902769	snp	C/G	0.02016	0.0983543	intron-variant	SPSB1	GRCh38.p7	1:9340302	GGGAAGGCAGGGACA[C/G]TGGTGTTTGGGGACT	80176
rs74978644	snp	C/T	0.0236746	0.106192	intron-variant	SPSB1	GRCh38.p7	1:9342570	CAAACGTCCCTCTCC[C/T]GCCTCATCCTGCCTT	80176
rs75060985	snp	C/T	0.0596104	0.162024	intron-variant	SPSB1	GRCh38.p7	1:9297796	TGTAGAGTTAGGGAT[C/T]CAAAGGCTTAGGGAC	80176
rs75069994	snp	A/G	0.210605	0.246877	intron-variant	SPSB1	GRCh38.p7	1:9357749	ATGTGTAGGGGCACC[A/G]TGCTGGTGTGGGAGG	80176
rs75076030	snp	A/G	0.00438332	0.0466095	intron-variant	SPSB1	GRCh38.p7	1:9343351	CGTCGAAAGGGAATC[A/G]TACAATGTGTGACCT	80176
rs75119470	snp	A/G	0.021333	0.101051	intron-variant	SPSB1	GRCh38.p7	1:9367253	AGAGGGCTCGCCCAG[A/G]TGCCCAGCCCAGGGT	80176
rs75478423	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9323684	GCGTCTCCAGGCACC[G/T]AGAGCCCATGTTGGG	80176
rs75479523	snp	C/T	0.0596104	0.162024	intron-variant	SPSB1	GRCh38.p7	1:9297569	TATTAGGATGTGGAA[C/T]GAACATGAAGTTGGA	80176
rs75480078	snp	A/G	0.0228947	0.104514	intron-variant	SPSB1	GRCh38.p7	1:9349479	GCCAAGGGACGTGGA[A/G]CGTGAGAGGCTGAGG	80176
rs75504344	snp	A/C/T	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9340236	TGTCTGGTTTTCCAT[A/C/T]TGGGGGCCTAGAGAA	80176
rs75515177	snp	C/G	0.0460142	0.144533	intron-variant	SPSB1	GRCh38.p7	1:9332262	GATCTAAGGGACTTG[C/G]AGACTCTTGCAGTGG	80176
rs75573311	snp	A/G	0.0554779	0.157039	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9292175	CGAGGGGTGGGGAAT[A/G]CCAGGAGATTTTGCT	80176
rs75581935	snp	C/T	0.0402882	0.136092	intron-variant	SPSB1	GRCh38.p7	1:9304633	GAATTGCAGGTGCCT[C/T]GGGTTCCCAGCTAGT	80176
rs75604135	snp	C/T	0.0279526	0.114869	intron-variant	SPSB1	GRCh38.p7	1:9316141	TTCTTCCTGACTCAG[C/T]CTTGCCCTGGGCTGG	80176
rs75632057	snp	C/T	0.0566069	0.158427	intron-variant	SPSB1	GRCh38.p7	1:9362358	GGCGTCCTTCCCCAG[C/T]TGACAAGGACAAAGG	80176
rs75651962	in-del	-/AA			intron-variant	SPSB1	GRCh38.p7	1:9314008	GGTGAAATCCCTTTT[-/AA]CCACTAAAAATACAA	80176
rs75674212	snp	A/G	0.0770498	0.180522	intron-variant	SPSB1	GRCh38.p7	1:9346626	AAACACCATCGGGGG[A/G]TTGCCGGCAGGTGCT	80176
rs75677526	snp	C/T	0.0107246	0.0724382	intron-variant	SPSB1	GRCh38.p7	1:9363214	CGCCATCAGTTTCCT[C/T]CTGCAAGATCAAGGA	80176
rs75678632	snp	A/G	0.00279162	0.0372561	intron-variant	SPSB1	GRCh38.p7	1:9331978	GGACCAAAAACAAAT[A/G]TGCCAAACTGTTGAC	80176
rs75743450	snp	C/G	0.0429648	0.14013	intron-variant	SPSB1	GRCh38.p7	1:9331871	TGGGAGGTTGAGCTT[C/G]TTTTCCTACAAGTTT	80176
rs75746801	snp	A/C/G	0.0345466	0.126924	intron-variant	SPSB1	GRCh38.p7	1:9307872	GTCTTCGGGGTGCGC[A/C/G]TGGCCCCTCCCAGGC	80176
rs75758127	snp	A/G	0.039522	0.134904	intron-variant	SPSB1	GRCh38.p7	1:9313817	GGCTGAGTGAATGGA[A/G]GAGTGTTATCGGAGA	80176
rs75776157	snp	A/G	0.0379877	0.132479	intron-variant	SPSB1	GRCh38.p7	1:9317384	ATAAAAGTCATCACC[A/G]AAATCAATCTGACTC	80176
rs75780251	snp	C/T	0.0263992	0.111815	intron-variant	SPSB1	GRCh38.p7	1:9300806	TGGTCCAAAGGCCCA[C/T]GGTTCTTACTTTGCC	80176
rs75830710	snp	A/C/G	0.00676609	0.0577691	intron-variant	SPSB1	GRCh38.p7	1:9339248	TTGCCTAGAATATTC[A/C/G]AGAACTCCAGGTCCC	80176
rs75850835	snp	A/G	0.499918	0.00638925	intron-variant	SPSB1	GRCh38.p7	1:9357220	ATGGATCAGTGAATG[A/G]ATGGATGGATGGATG	80176
rs75875492	snp	C/T	0.0107246	0.0724382	intron-variant	SPSB1	GRCh38.p7	1:9329220	GGGCCCGAGCACAGC[C/T]GGTTGAGGGTTTGTG	80176
rs75876526	snp	A/G	0.0209421	0.100162	intron-variant	SPSB1	GRCh38.p7	1:9311288	GACCCAGGAGGCTGC[A/G]TCTGAGCCGAGTCCT	80176
rs75928355	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9362278	TGGTCATATGAGGAC[C/T]GCAGGCTCTCAGAGT	80176
rs75946798	snp	C/G/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9316563	TGGCGAGGAGGGGGG[C/G/T]GCTGATCGAAGCGGG	80176
rs76009333	snp	A/G	0.0287284	0.116357	intron-variant	SPSB1	GRCh38.p7	1:9323806	TCCAGGGTCATGAGG[A/G]ATACATTTCTTCTGC	80176
rs76049555	snp	A/C	0.0368353	0.130617	intron-variant	SPSB1	GRCh38.p7	1:9317267	AAGCACTGGAGAGGG[A/C]GGAGGAAGGGAAGAA	80176
rs76120085	snp	C/G	0.02016	0.0983543	intron-variant	SPSB1	GRCh38.p7	1:9365985	AGCAGGGCCGCGCAG[C/G]CTTCCAACGCTCAGA	80176
rs76157888	snp	C/T	0.0287284	0.116357	intron-variant	SPSB1	GRCh38.p7	1:9319627	GCTGATGTTCCGTAC[C/T]GGGCTGGTATTCCGT	80176
rs76171956	snp	A/C	0.5	0	intron-variant	SPSB1	GRCh38.p7	1:9325229	CTCCCACCACCACCC[A/C]CCCCCCCCGCCCCGC	80176
rs76172944	snp	G/T	0.5	0	intron-variant	SPSB1	GRCh38.p7	1:9363718	ATTTTTTTTTTTTTG[G/T]AGATGGAGTCTCATT	80176
rs76253052	in-del	-/GTGTGT			intron-variant	SPSB1	GRCh38.p7	1:9348957	TGTGTGTGTGTGTGT[-/GTGTGT]GTATATGTGCGTGTG	80176
rs76269435	snp	A/G	0.031825	0.122064	intron-variant	SPSB1	GRCh38.p7	1:9308541	TCCCATGCTGGGGCC[A/G]GCATTTAGTTTAGGG	80176
rs76402707	snp	C/G	0.0267878	0.112589	intron-variant	SPSB1	GRCh38.p7	1:9326141	GGGTGGAATGTTCTT[C/G]GTGGGGCTGAATTTA	80176
rs76405939	snp	C/T	0.0279526	0.114869	intron-variant	SPSB1	GRCh38.p7	1:9342849	AGGCCTGGACTGCAG[C/T]AATTCTGCTCTCGAA	80176
rs76473395	snp	A/G	0.13446	0.221699	intron-variant	SPSB1	GRCh38.p7	1:9337550	GTGCACCCTAACCTC[A/G]CACCCCAGCCCTCTG	80176
rs76583735	snp	C/T	0.0256215	0.110247	intron-variant	SPSB1	GRCh38.p7	1:9311329	TGGGGTTTCTTTCTT[C/T]CCCCTGATGGGTCTC	80176
rs76604837	snp	C/T	0.00358779	0.0422022	intron-variant	SPSB1	GRCh38.p7	1:9306373	TTGTGATGTCCAGCC[C/T]GGAGGAGGTGGAAGA	80176
rs76664662	snp	C/G	0.0387552	0.1337	intron-variant	SPSB1	GRCh38.p7	1:9361692	GATTCCTCCTCAAGG[C/G]TCGAGGCACAAGGCC	80176
rs76667926	snp	C/T	0.0182019	0.0936463	intron-variant	SPSB1	GRCh38.p7	1:9342337	GCGTAGTGACAAGTC[C/T]AGAAACTGTGTGCAT	80176
rs76773239	snp	C/T	0.0429648	0.14013	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9368289	TCCTTCCACCTGTGC[C/T]CTCCCTGGGATATGT	80176
rs76827042	snp	A/C	0.5	0	intron-variant	SPSB1	GRCh38.p7	1:9329706	TCAAAAACAACAACA[A/C]AAAAAAAAAAAAAAA	80176
rs76910624	snp	A/C	0.00199481	0.0315187	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9368075	TGGCAGATAAAGCTC[A/C]GGACGTCAAAAACTC	80176
rs76913841	snp	C/T	0.0387552	0.1337	intron-variant	SPSB1	GRCh38.p7	1:9342367	TCAGCCTGGGGCACC[C/T]CTAGCTGTGGGCAGA	80176
rs76943294	snp	A/G	0.0248432	0.108648	intron-variant	SPSB1	GRCh38.p7	1:9304778	CTCAACGCTCAAGCA[A/G]TCCTCCCACCTCAGC	80176
rs76961015	snp	C/T	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9351117	CTGGGCCAAATCTGG[C/T]CCACTGTCTATTTTT	80176
rs76967182	in-del	-/TTT			intron-variant	SPSB1	GRCh38.p7	1:9306950	TTTTTTTTTTTAAGT[-/TTT]GGAATCTCGCTCTGT	80176
rs77035363	snp	A/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9336374	TGGGATTACAGGCAC[A/G]CACCACTATGCCCGG	80176
rs77174154	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9295582	CTGGGCTGCTGCAGA[A/G]TCTCACCCCCTTGGA	80176
rs77176763	snp	C/T	0.079617	0.182947	intron-variant	SPSB1	GRCh38.p7	1:9333840	GGCTTTCCTCTCCAG[C/T]GCGGCTCCGGGGAAA	80176
rs77208948	snp	A/G	0.00358779	0.0422022	intron-variant	SPSB1	GRCh38.p7	1:9318258	CAGCAGAACAGTGAC[A/G]GGTCCTCCGCCCGCT	80176
rs77302022	snp	A/G	0.00993419	0.0697739	intron-variant	SPSB1	GRCh38.p7	1:9306597	ACTAGGGCAACTCTG[A/G]GCCTCCCTGCCACCC	80176
rs77369104	in-del	-/T	0.264084	0.249603	intron-variant	SPSB1	GRCh38.p7	1:9331289	TGTCATAAATACCCG[-/T]TTATGGATCTCCTTC	80176
rs77387534	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9362196	CCTCCCTCCCTCCCT[C/T]CCTTCCTTCCTTCCA	80176
rs77390888	snp	C/T	0.165527	0.235296	intron-variant	SPSB1	GRCh38.p7	1:9323045	TGTCTGGCTGTCACT[C/T]TTTGATGCTGGTGGT	80176
rs77412498	snp	A/G	0.5	0	intron-variant	SPSB1	GRCh38.p7	1:9329723	AAAAAAAAAAAAAAA[A/G]AGAAAAGAAAGAAAG	80176
rs77453762	snp	A/G	0.0422008	0.138995	intron-variant	SPSB1	GRCh38.p7	1:9330780	TAAGACGTGCAGTTC[A/G]GTAGCGTTGAGTACA	80176
rs77534138	snp	A/G	0.00279162	0.0372561	intron-variant	SPSB1	GRCh38.p7	1:9312352	TTTATGAGACAAAGC[A/G]GGGAGTCCCTGACCT	80176
rs77536890	snp	A/G	0.031825	0.122064	intron-variant	SPSB1	GRCh38.p7	1:9308282	CCTAGCAAGGGGGCC[A/G]TTTGCCCTGGGCCCA	80176
rs77641272	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9330970	AAAAAAAATCCTAAA[C/T]CTTTTATTGAAGGAT	80176
rs77674844	snp	A/G	0.0368353	0.130617	intron-variant	SPSB1	GRCh38.p7	1:9305034	CTTCACCTGCCTCCT[A/G]CGCCCAGACCCATCT	80176
rs77685128	snp	G/T	0.0263992	0.111815	intron-variant	SPSB1	GRCh38.p7	1:9312585	TGGGGGAGGGCCGCA[G/T]TCTCCCAAGTTTCCT	80176
rs77741033	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9298454	TAAGTGAATGAATAA[A/G]TGAATGAATGAATGA	80176
rs77741734	snp	C/T	0.0509478	0.151255	intron-variant	SPSB1	GRCh38.p7	1:9320453	ATCTCCGCCATTTGA[C/T]TGGGAGGCCTCTCGA	80176
rs77770568	snp	C/T	0.040671	0.13668	intron-variant	SPSB1	GRCh38.p7	1:9297369	AGGGTTGGAAAAACC[C/T]ACCTGTGACAAGGGC	80176
rs77777406	snp	C/G	0.0298908	0.118541	intron-variant	SPSB1	GRCh38.p7	1:9341410	TTGCCTGCCTCCCCC[C/G]ACTAGACTGAGCTCC	80176
rs77856416	snp	A/G	0.210301	0.246828	intron-variant	SPSB1	GRCh38.p7	1:9360206	CTGCTTAGAGGCCAG[A/G]AGGGTGGGGGCTGAA	80176
rs77905532	in-del	-/A	0.49657	0.041273	intron-variant	SPSB1	GRCh38.p7	1:9320889	TGAGCTCTGGCCACG[-/A]AAGGCTGGCCTGATG	80176
rs77938148	snp	A/G	0.00953873	0.0683987	intron-variant	SPSB1	GRCh38.p7	1:9324226	GCTGGAATGGGCCTA[A/G]GTGGGAGGGACTTTG	80176
rs78006041	snp	C/G/T	0.0848645	0.188218	intron-variant	SPSB1	GRCh38.p7	1:9344281	ATTCAGAAAGTCTAA[C/G/T]GGGATCAGGAATTTG	80176
rs78152139	snp	C/T	0.0368353	0.130617	intron-variant	SPSB1	GRCh38.p7	1:9316834	TCCACCTCGGTTCTC[C/T]CTGCTCCTATGACCT	80176
rs78237381	snp	A/G	0.0547245	0.156101	intron-variant	SPSB1	GRCh38.p7	1:9328012	TGGAGTGCTGCAATC[A/G]CACTTACGCTTTGGG	80176
rs78318605	snp	A/C	0.5	0	intron-variant	SPSB1	GRCh38.p7	1:9347965	TTTTTTTTTTTTTTA[A/C]ACAGAATCTCGCTCT	80176
rs78325247	snp	A/G	0.0271762	0.113356	intron-variant	SPSB1	GRCh38.p7	1:9342560	CCTAGGAATCCAAAC[A/G]TCCCTCTCCCGCCTC	80176
rs78366052	snp	C/T	0	0	intron-variant	SPSB1	GRCh38.p7	1:9366580	GTGTCCTCAGTTCTT[C/T]TTTTTTTTTTTTTGG	80176
rs78536435	snp	C/T	0.0271762	0.113356	intron-variant	SPSB1	GRCh38.p7	1:9314681	CGTCTTGTTTTTCTC[C/T]GGGAAGAATCAGCCT	80176
rs78541188	snp	A/G	0.0154538	0.0865337	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9292077	GGTTATGGTAAAGAC[A/G]CAGTAACTACGGAAG	80176
rs78544625	snp	A/G	0.00358779	0.0422022	intron-variant	SPSB1	GRCh38.p7	1:9339413	TCCTCAGGTAATTCC[A/G]GGGCGAGTCTGGAGG	80176
rs78564422	snp	C/T	0.0189856	0.0955633	intron-variant	SPSB1	GRCh38.p7	1:9326136	AGGTCGGGTGGAATG[C/T]TCTTGGTGGGGCTGA	80176
rs78666899	snp	A/G	0.210605	0.246877	intron-variant	SPSB1	GRCh38.p7	1:9360180	GAGGAGAAGAGGGCT[A/G]AGGCTGAGCCCTGCT	80176
rs78678520	snp	C/T	0.0123036	0.0774623	intron-variant	SPSB1	GRCh38.p7	1:9364780	AAGAGCAGTGGTCCC[C/T]CTTCTTTTGTTTATT	80176
rs78824586	in-del	-/TTT			intron-variant	SPSB1	GRCh38.p7	1:9330714	CTGAACTTTTTTTTT[-/TTT]AATCGTGGTAAAACA	80176
rs78841739	snp	C/G	0.0505692	0.150756	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9368632	TTTCCCAAGTGCATC[C/G]TCAGAAGCTCTGGGT	80176
rs78908140	snp	C/G	0.226484	0.248892	intron-variant	SPSB1	GRCh38.p7	1:9348347	ATAATGAAAGCAAAC[C/G]GTGGCTGTATCCAGA	80176
rs78920487	snp	C/G/T	0.5	0	intron-variant	SPSB1	GRCh38.p7	1:9364574	AGTCCCACCCCATCA[C/G/T]GAGGGGTCTGTGGGA	80176
rs78930438	snp	A/G	0.0425829	0.139564	intron-variant	SPSB1	GRCh38.p7	1:9344199	AAACCAGTGGTTCTC[A/G]ATCTCTGGCCTCATC	80176
rs78942108	snp	A/G/T	0.00119737	0.0244387	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291279	CAATCTCTGCCTCCC[A/G/T]GGTTCACACCATTCT	80176
rs78995222	snp	C/T	0.0539704	0.155153	intron-variant	SPSB1	GRCh38.p7	1:9303534	TTCTTTCCTCTCTTA[C/T]TCCTTATTCTTAGAA	80176
rs78998002	snp	A/G	0.031825	0.122064	intron-variant	SPSB1	GRCh38.p7	1:9308373	AGGGCCCCCGGAGCC[A/G]CGGTGCCCTGACTGT	80176
rs79124771	snp	C/T	0.0383715	0.133092	intron-variant	SPSB1	GRCh38.p7	1:9320584	TACACAGAGGAAGCA[C/T]GCAGCCCTCTCTTCC	80176
rs79247606	snp	A/T	0.0178098	0.0926698	intron-variant	SPSB1	GRCh38.p7	1:9362020	CGGCTCCCAGATGGG[A/T]TTGGTGTGGTTTGTC	80176
rs79517232	snp	A/C/G	0.0185938	0.0946107	intron-variant	SPSB1	GRCh38.p7	1:9308844	CTGCGACAGTGGAAC[A/C/G]TGCCAGTCCTGTTGA	80176
rs79517478	snp	A/T	0.138546	0.223781	intron-variant	SPSB1	GRCh38.p7	1:9334862	ATTCACTCATATAGC[A/T]TGTATCAAAATGTCC	80176
rs79606357	snp	C/T	0.078151	0.181571	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291995	CTCTGGACAGCTGGC[C/T]TCGGGCCAGGCACTG	80176
rs79623822	snp	C/T	0.5	0	intron-variant	SPSB1	GRCh38.p7	1:9310194	CATCTGTGATGATGC[C/T]CCTGCACCTGCCGTG	80176
rs79643218	snp	A/G	0.0298908	0.118541	intron-variant	SPSB1	GRCh38.p7	1:9308279	GCACCTAGCAAGGGG[A/G]CCATTTGCCCTGGGC	80176
rs79655866	snp	A/G	0.00279162	0.0372561	intron-variant	SPSB1	GRCh38.p7	1:9323811	GGTCATGAGGAATAC[A/G]TTTCTTCTGCTGTTG	80176
rs79656366	snp	A/G	0.031825	0.122064	intron-variant	SPSB1	GRCh38.p7	1:9308166	TCAGGCCCAAAGGGG[A/G]TGGACTGCCTCTCAT	80176
rs79679718	snp	C/T	0.5	0	intron-variant	SPSB1	GRCh38.p7	1:9307757	TTATTTGTATCTTTT[C/T]CCGTTGATCTATTAA	80176
rs79682502	snp	C/T	0.0119091	0.0762411	intron-variant	SPSB1	GRCh38.p7	1:9307339	ACTATCCCCTCTGTC[C/T]AGTTCCAAACCATCT	80176
rs79819093	snp	A/T	0	0	intron-variant	SPSB1	GRCh38.p7	1:9347963	TTTTTTTTTTTTTTT[A/T]AAACAGAATCTCGCT	80176
rs79829952	snp	C/T	0.0283406	0.115616	intron-variant	SPSB1	GRCh38.p7	1:9343339	TCCTGGTCATTTCGT[C/T]GAAAGGGAATCGTAC	80176
rs79831454	snp	C/T	0.0364509	0.129988	intron-variant	SPSB1	GRCh38.p7	1:9319648	GGTATTCCGTTCCGG[C/T]TGGTGCAGAGGATGC	80176
rs79868898	snp	A/G	0.0429648	0.14013	intron-variant	SPSB1	GRCh38.p7	1:9326646	AGGCTCCTGTGCCCC[A/G]TCCCAGAAAGAAGCC	80176
rs79905773	snp	G/T	0.5	0	intron-variant	SPSB1	GRCh38.p7	1:9349428	GTAGGTGAGTGTGGG[G/T]TCAGGGGGCTGTCCC	80176
rs80014315	snp	A/C	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9337264	CAGCTCAATGGCCTT[A/C]CCCCTCCAAGGCAGA	80176
rs80043631	snp	A/G	0.00557542	0.0525036	intron-variant	SPSB1	GRCh38.p7	1:9333157	TTCGGTGAGAACCTT[A/G]GTCTGCCCTGTTCAG	80176
rs80074616	snp	G/T	0.0287284	0.116357	intron-variant	SPSB1	GRCh38.p7	1:9316769	GCGGCATTGGGTCTG[G/T]GTCTGGGGGCCGCAG	80176
rs80087011	snp	G/T	0.00358779	0.0422022	intron-variant	SPSB1	GRCh38.p7	1:9303602	TTACATCATAGTATT[G/T]AAGTTATTGAGTATC	80176
rs80092544	snp	C/T	0.375	0.216506	intron-variant	SPSB1	GRCh38.p7	1:9310195	ATCTGTGATGATGCT[C/T]CTGCACCTGCCGTGG	80176
rs80118388	snp	C/T	0.0418186	0.138422	intron-variant	SPSB1	GRCh38.p7	1:9349655	AACTCGTGCCACACA[C/T]AATCCGCCACCAGCA	80176
rs80127204	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9298452	AATAAGTGAATGAAT[A/G]AGTGAATGAATGAAT	80176
rs80134066	snp	C/T	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9307361	AAACCATCTTCATCC[C/T]GCCGGAAGGAAACCC	80176
rs80174441	snp	C/T	0.0368353	0.130617	intron-variant	SPSB1	GRCh38.p7	1:9319537	GGCCACTGTGCTCCC[C/T]GCTGAAGTCGAGTGG	80176
rs80232913	snp	G/T	0.0410537	0.137264	intron-variant	SPSB1	GRCh38.p7	1:9338478	AGGACAGCACTTGCT[G/T]GGGAGGACAGGGGGC	80176
rs80237880	snp	C/G	0.0178098	0.0926698	intron-variant	SPSB1	GRCh38.p7	1:9349801	TCTCTCTTGACCCTT[C/G]CTGATCTTTACTTTA	80176
rs80276030	snp	A/T	0.00279162	0.0372561	intron-variant	SPSB1	GRCh38.p7	1:9329908	ATGAGGCCTTTGGAA[A/T]CTTTTCTGGGACTGA	80176
rs80329099	snp	A/T	0.0240643	0.107019	intron-variant	SPSB1	GRCh38.p7	1:9332000	ACTGTTGACAGTTTG[A/T]GTGTTGAAAATATGT	80176
rs80331445	snp	C/T	0.00597247	0.0543191	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9368460	CAATCTGGGTGTCTT[C/T]GGGGGCCCGTCTGGA	80176
rs111214144	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9294107	CTGTGTGTCTTTGTG[A/T]GTGTCTGTGTGTGAG	80176
rs111305341	snp	A/G	0.0322114	0.122752	intron-variant	SPSB1	GRCh38.p7	1:9309700	ATATAAAAATTAGTC[A/G]GGGATGGTGGTGCAT	80176
rs111343382	in-del	-/TGTGTG	0.359364	0.22481	intron-variant	SPSB1	GRCh38.p7	1:9348938	TCACTCGTGCAAGAA[-/TGTGTG]TGTGTGTGTGTGTGT	80176
rs111352951	snp	A/G	0.0898077	0.191933	intron-variant	SPSB1	GRCh38.p7	1:9361018	CCACCCAAGTCCCCC[A/G]TCCCGGGAGAGTTGG	80176
rs111354825	in-del	-/C	0.5	0	intron-variant	SPSB1	GRCh38.p7	1:9329706	CAAAAACAACAACAA[-/C]AAAAAAAAAAAAAAA	80176
rs111381972	snp	A/G	0.00835141	0.0640778	intron-variant	SPSB1	GRCh38.p7	1:9358483	CTAGGTGTCAGAAAT[A/G]AGTGGCACCACGTCC	80176
rs111396393	snp	A/G	0.5	0	intron-variant	SPSB1	GRCh38.p7	1:9338590	GTTTCTGTTCATTTC[A/G]GGACAAGTTGCCTGG	80176
rs111402956	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9348225	GCTGGGATTACAGGC[G/T]TGAGCCACCGCGGCA	80176
rs111476890	snp	A/G	0.031825	0.122064	intron-variant	SPSB1	GRCh38.p7	1:9309381	GGAGTGCAGTGGTGC[A/G]GTCACAGCTCACTGC	80176
rs111544321	snp	C/G	0.5	0	intron-variant	SPSB1	GRCh38.p7	1:9333907	CTCAGAGGCAGGTGG[C/G]GCCTGGCCAGGGATG	80176
rs111577931	snp	C/T	0.0678174	0.1712	intron-variant	SPSB1	GRCh38.p7	1:9313950	GGAGGCCTAGGCGGG[C/T]GGATCACTTGAGGTC	80176
rs111585094	snp	G/T	0.5	0	intron-variant	SPSB1	GRCh38.p7	1:9365333	TGTTGCTCAGGCTGG[G/T]CTCAAACTCCTGGGC	80176
rs111608800	snp	A/G	0.256061	0.249927	intron-variant	SPSB1	GRCh38.p7	1:9361188	TTTTTTTTTTTAGAG[A/G]TGGGGTCTCACTATG	80176
rs111651835	in-del	-/CACACATACACAAACGTGTGCATG/TG	0.452227	0.146984	intron-variant	SPSB1	GRCh38.p7	1:9296594	GTGCACATGTGTACA[-/CACACATACACAAACGTGTGCATG/TG]CACACATACATATGC	80176
rs111669188	snp	G/T	0	0	intron-variant	SPSB1	GRCh38.p7	1:9342460	GGATCCCAGTGGCTT[G/T]TCAATTCGCTGATAG	80176
rs111674995	in-del	-/A	0.5	0	intron-variant	SPSB1	GRCh38.p7	1:9335502	GCGAGTCTCTGTCTC[-/A]AAAAAAAAAAAAAGA	80176
rs111696305	snp	A/G	0.5	0	intron-variant	SPSB1	GRCh38.p7	1:9345389	TGTGTGAACCAGATG[A/G]GCCCAGTGTGTTACC	80176
rs111703618	snp	A/G	0.5	0	intron-variant	SPSB1	GRCh38.p7	1:9348939	CACTCGTGCAAGAAT[A/G]TGTGTGTGTGTGTGT	80176
rs111726806	snp	A/G	0.0337553	0.125452	utr-variant-5-prime	SPSB1	GRCh38.p7	1:9355751	CCATTAGGCAATACT[A/G]AACACTGCGCAGCTT	80176
rs111750743	snp	C/T	0.031825	0.122064	intron-variant	SPSB1	GRCh38.p7	1:9308393	GCCCTGACTGTGGGT[C/T]GGGGGACAGTTTCTA	80176
rs111762386	snp	C/G	0.00517822	0.0506191	intron-variant	SPSB1	GRCh38.p7	1:9301929	CTTATTCTGGATACA[C/G]ATTCGTCTTCCCTGC	80176
rs111801874	snp	C/T	0.00874735	0.0655527	intron-variant	SPSB1	GRCh38.p7	1:9316635	ACCTTAGAGCCCACC[C/T]GTTCCCGCCATCTTG	80176
rs111816134	snp	C/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9342704	TCTGGGGCACACATC[C/T]GAGATGCAGGCACAC	80176
rs111921632	snp	C/T	0.5	0	intron-variant	SPSB1	GRCh38.p7	1:9338192	GGTTGGGGGGTGCCA[C/T]TCAGCTCTCCCCTAC	80176
rs111945803	snp	C/T	0.5	0	intron-variant	SPSB1	GRCh38.p7	1:9328455	ATGATGTTTCCTAAC[C/T]CAGCTCAGACATGAT	80176
rs111957386	snp	A/G	0.031825	0.122064	intron-variant	SPSB1	GRCh38.p7	1:9309678	TGAAACCCCGTCTCT[A/G]CTAAAAATATAAAAA	80176
rs111998043	snp	C/T	0.5	0	intron-variant	SPSB1	GRCh38.p7	1:9332356	ATTTACAATGTTTGG[C/T]GCTAATGTGGGAAGC	80176
rs112042224	snp	C/T	0.5	0	intron-variant	SPSB1	GRCh38.p7	1:9295674	GGAAGCCAGCGCTGC[C/T]CTCCCACCCCCATGG	80176
rs112076560	in-del	-/GTGA	0.498754	0.0249289	intron-variant	SPSB1	GRCh38.p7	1:9294269	TCCACACGTGTCTCT[-/GTGA]GTGTCTGTCTCTGTG	80176
rs112154300	snp	C/T	0.0271762	0.113356	intron-variant	SPSB1	GRCh38.p7	1:9352291	TGGCTCTTTCTGGGA[C/T]GGGGCTGGCCCAGCC	80176
rs112159091	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9350771	GAAACTCACCAACTG[C/T]TCAGCAGTCCCAGGC	80176
rs112176700	snp	C/T	0.0433465	0.140692	intron-variant	SPSB1	GRCh38.p7	1:9343828	TCTCGCTCTGTTGCC[C/T]AGGCTGGAGTGCAGT	80176
rs112184797	in-del	-/T	0.260609	0.249775	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9369206	TTATTATTTTGACGG[-/T]TTTTTTTTTCGGGGC	80176
rs112222084	in-del	-/C	0.5	0	intron-variant	SPSB1	GRCh38.p7	1:9325493	AGGTGGTGTGGGCGA[-/C]CCTAGGCCCTGCTTC	80176
rs112386829	snp	C/T	0.0429648	0.14013	intron-variant	SPSB1	GRCh38.p7	1:9338140	GGTCCCCTGTCCCCT[C/T]GCTCCTCCCCCCAGA	80176
rs112430353	snp	A/G	0.5	0	intron-variant	SPSB1	GRCh38.p7	1:9357165	TGGATGGATGGGTGG[A/G]TGGATGGGTGGATGG	80176
rs112439407	snp	A/G	0.5	0	intron-variant	SPSB1	GRCh38.p7	1:9294335	GTCTGTGTGTCTCCA[A/G]GTGTGTGTCTGTGTG	80176
rs112475092	snp	A/G	0.031825	0.122064	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9367675	CTTGGACCGGCATCC[A/G]TAGCCATGGACAGAG	80176
rs112547723	snp	C/T	0.00554992	0.0523847	synonymous-codon	SPSB1	GRCh38.p7	1:9356068	TTCATGGAACAACAA[C/T]GACCGATCGCTCAAT	80176
rs112557775	snp	A/G	0.0352966	0.128072	intron-variant	SPSB1	GRCh38.p7	1:9365464	TAAATGCATTATCAA[A/G]CCTAAGGTCCATTCT	80176
rs112572209	snp	A/T	0.5	0	intron-variant	SPSB1	GRCh38.p7	1:9346034	TGTCCCTGCCACTCA[A/T]GCTCAGGATGCTGGA	80176
rs112581193	snp	A/C	0.00636936	0.0560724	intron-variant	SPSB1	GRCh38.p7	1:9349465	GCTCAACCAGAGAGG[A/C]CAAGGGACGTGGAGC	80176
rs112612748	snp	C/T	0.0107246	0.0724382	intron-variant	SPSB1	GRCh38.p7	1:9321736	GCAGAGATCTTAAGA[C/T]GTGAATCACATGACT	80176
rs112613752	snp	G/T	0.5	0	intron-variant	SPSB1	GRCh38.p7	1:9312496	TATTAGTGCACACAT[G/T]TGGTCAGGCAGCCGT	80176
rs112664811	snp	C/T	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9342722	GATGCAGGCACACAT[C/T]CCGGACTCCTCCGGA	80176
rs112679489	snp	A/G	0.00438332	0.0466095	intron-variant	SPSB1	GRCh38.p7	1:9348620	CCTGGAGGAGCCCAC[A/G]AAACTGGAGGGATTT	80176
rs112742782	in-del	-/GAGTTCAAGACCA	0.447032	0.153878	intron-variant	SPSB1	GRCh38.p7	1:9318981	ATCACCTGAGGTCAT[-/GAGTTCAAGACCA]GCCTGGGCAACATGG	80176
rs112746214	snp	A/G	0.5	0	intron-variant	SPSB1	GRCh38.p7	1:9337413	CACACCTGGCCAGCC[A/G]CCTGCCCACCTAGCC	80176
rs112792913	snp	A/G	0.5	0	intron-variant	SPSB1	GRCh38.p7	1:9328535	TTCTTTCAATGCTTC[A/G]TTTTATAAACAGGGA	80176
rs112829068	snp	C/T	0.0429648	0.14013	intron-variant	SPSB1	GRCh38.p7	1:9334167	CTCGGCTCGTTGCAA[C/T]TTCCGCCTCCCGGGC	80176
rs112857746	snp	C/T	0.5	0	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291179	GGTCCTGAACTTCTT[C/T]TTTTTTTTTTTTTTT	80176
rs112871283	snp	A/G	0.5	0	intron-variant	SPSB1	GRCh38.p7	1:9357121	TGGATGAGTGGATGG[A/G]TGGATGGATGAGTGG	80176
rs112900779	snp	C/T	0.031825	0.122064	intron-variant	SPSB1	GRCh38.p7	1:9309527	TCTCGCCATGTTGCC[C/T]AGGCTCTCCCTTGCA	80176
rs112902759	snp	C/T	0.0103295	0.0711199	intron-variant	SPSB1	GRCh38.p7	1:9317083	CTTCCGGTGCTCTCG[C/T]GAAGGAAAGAGAGAA	80176
rs112903636	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9334165	ATCTCGGCTCGTTGC[A/T]ACTTCCGCCTCCCGG	80176
rs112919797	snp	A/G	0.5	0	intron-variant	SPSB1	GRCh38.p7	1:9336267	AGTTTCACTCTTGTT[A/G]CCCAGGCTGGAGTGC	80176
rs112928691	snp	G/T	0.02016	0.0983543	intron-variant	SPSB1	GRCh38.p7	1:9308290	GGGGGCCATTTGCCC[G/T]GGGCCCATCCTTGGT	80176
rs112938229	in-del	-/G	0.0923359	0.194016	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291376	ATTTGTAGTAGTGAC[-/G]GGGTTTCATCGTGTT	80176
rs112986265	snp	A/G	0.5	0	intron-variant	SPSB1	GRCh38.p7	1:9348292	CGCTCCTGTCTCGGC[A/G]GTAGTGCTGTGTCTA	80176
rs113020702	snp	A/G	0.0498117	0.149749	intron-variant	SPSB1	GRCh38.p7	1:9358293	TTGACAGCCACACAC[A/G]ATGTCTGTGGTACAG	80176
rs113202483	snp	A/G			synonymous-codon	SPSB1	GRCh38.p7	1:9367494	TCGCTCGGTGCGCCT[A/G]GCCCTGGGGAGGGAG	80176
rs113212787	snp	C/G	0.0539704	0.155153	intron-variant	SPSB1	GRCh38.p7	1:9357786	CTCCATGGCTGCCCA[C/G]CTGGGAGTCCGTGGT	80176
rs113224685	in-del	-/TTCTTA	0.0829062	0.185956	intron-variant	SPSB1	GRCh38.p7	1:9344670	TCATGAACGCTGCCC[-/TTCTTA]TTCTTATTCCCCCAG	80176
rs113225135	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9320425	CACGTGTGTGCAGAT[A/T]TGGGGTGGCCCCATC	80176
rs113233052	snp	C/T	0.5	0	intron-variant	SPSB1	GRCh38.p7	1:9325188	CCAAGAAGACCTGTA[C/T]TCCGCCCTCCGGCCT	80176
rs113245420	in-del	-/A	0	0	intron-variant	SPSB1	GRCh38.p7	1:9310710	TAAAAAAAAAAAAAG[-/A]GAGACCTGGGCAGCA	80176
rs113282889	snp	C/T	0.00557542	0.0525036	intron-variant	SPSB1	GRCh38.p7	1:9359107	TCAGAGCATCACAGC[C/T]GGGCGCTATTAGTCA	80176
rs113381958	snp	G/T	0.5	0	intron-variant	SPSB1	GRCh38.p7	1:9295828	ATTTTGTATCAATTT[G/T]TCTCGAGAAATAGGT	80176
rs113409786	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9319890	CTGCAGGTGGGAAGC[A/G]GCCTCCCCGCCTATC	80176
rs113426738	snp	C/G	0.0166325	0.0896639	intron-variant	SPSB1	GRCh38.p7	1:9321106	TTCAGCCTTTTCCTT[C/G]TACCCCTCCCCCGAA	80176
rs113461150	snp	C/T	0.444444	0.157135	intron-variant	SPSB1	GRCh38.p7	1:9359034	GGTGAGTGGGGAATA[C/T]GAGAATGGGAATCAG	80176
rs113474552	snp	A/G	0.00716266	0.059414	intron-variant	SPSB1	GRCh38.p7	1:9319731	AGCCCCCAAAGGTCC[A/G]CTGTAGTGAAGGGAG	80176
rs113498475	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9336660	GCCTGAGTTCACCCG[A/T]GGCGCTGGGCTAGTG	80176
rs113499438	snp	C/T	0.0119091	0.0762411	intron-variant	SPSB1	GRCh38.p7	1:9299774	ATGAGCCACTGCGCC[C/T]GGGCCGACATCATCT	80176
rs113593781	snp	C/T	0.5	0	intron-variant	SPSB1	GRCh38.p7	1:9319481	TGGGATGAGAGGCTC[C/T]GAGGCCCTGCTGTCC	80176
rs113629973	snp	A/G	0.0146672	0.084371	intron-variant	SPSB1	GRCh38.p7	1:9308329	GGATACCCAGGTCCT[A/G]CATACCCAGCAGTAG	80176
rs113632654	snp	A/C	0.00676609	0.0577691	intron-variant	SPSB1	GRCh38.p7	1:9320348	CTCCTCCATCCCAGC[A/C]AGATGGCTGAAAGCT	80176
rs113702200	snp	C/T	0.0130921	0.0798413	intron-variant	SPSB1	GRCh38.p7	1:9308455	GAGAGAAAACCTAAG[C/T]TGTCATCAACTGGGG	80176
rs113710077	snp	C/G	0.031825	0.122064	intron-variant	SPSB1	GRCh38.p7	1:9309626	GACGGGTGGATCACC[C/G]GAGGTCAGGAGTTTG	80176
rs113777822	snp	A/G	0.5	0	intron-variant	SPSB1	GRCh38.p7	1:9357117	TGGATGGATGAGTGG[A/G]TGGATGGATGGATGA	80176
rs113778402	snp	C/T	0.5	0	intron-variant	SPSB1	GRCh38.p7	1:9302076	CACTGGGATCATGTG[C/T]AGGGAATTGGCCGGT	80176
rs113916340	snp	C/T	0.0337553	0.125452	intron-variant	SPSB1	GRCh38.p7	1:9355409	CCTGGTTCTGTGGCA[C/T]CATGGCCTTCCGCCC	80176
rs113928555	in-del	-/TC/TCTC/TCTCTC	0.241637	0.253569	intron-variant	SPSB1	GRCh38.p7	1:9299468	CACAGTGAGACGTCA[-/TC/TCTC/TCTCTC]TCTCTCTCTCTCTCT	80176
rs113996696	snp	A/C	0.00874735	0.0655527	intron-variant	SPSB1	GRCh38.p7	1:9300166	TCCAGTAGTGTCAGG[A/C]CTGTGAAGGTATCCC	80176
rs113999081	snp	C/T	0.0475351	0.146656	intron-variant	SPSB1	GRCh38.p7	1:9339386	CAGGCCAGGTTCTGG[C/T]AGGACCCAGGGTCCT	80176
rs113999310	snp	A/G	0.0429648	0.14013	intron-variant	SPSB1	GRCh38.p7	1:9325375	TCTCAATGAATGAGG[A/G]GCCTGGAAGGCAGAC	80176
rs114004713	snp	C/T	0.48435	0.0870631	intron-variant	SPSB1	GRCh38.p7	1:9330476	GTCTCAAAATAATAA[C/T]AATAATAATAATAAT	80176
rs114121947	snp	C/T	0.00795532	0.062565	intron-variant	SPSB1	GRCh38.p7	1:9296528	CTCACCTCGCATGCA[C/T]ACACATACACATACT	80176
rs114122590	snp	C/T	0.084364	0.187256	intron-variant	SPSB1	GRCh38.p7	1:9320976	CTTAAAATCTCCTTC[C/T]CGAGTCCCTGGCTGC	80176
rs114123705	snp	C/T	0.0154538	0.0865337	intron-variant	SPSB1	GRCh38.p7	1:9293783	GTGGCGTCCAGGTTC[C/T]GGTGAGGACGGGACG	80176
rs114127976	snp	A/G	0.0119091	0.0762411	intron-variant	SPSB1	GRCh38.p7	1:9319609	ATGCTGTGTCTCACG[A/G]TGGCTGATGTTCCGT	80176
rs114134468	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9342089	GAAGCTCATTCTAAC[C/G]TGTCTTAGGGGCTTA	80176
rs114135017	snp	C/T	0.0337553	0.125452	intron-variant	SPSB1	GRCh38.p7	1:9362411	CTCTTTCGTAAGAAC[C/T]GCGTAGTGTAGAGGA	80176
rs114156651	snp	C/T	0.00398564	0.0444627	intron-variant	SPSB1	GRCh38.p7	1:9307312	CATTTGGTATATTCA[C/T]AATGTCGTGCAACTA	80176
rs114161890	snp	C/G	0.0364509	0.129988	intron-variant	SPSB1	GRCh38.p7	1:9319490	AGGCTCCGAGGCCCT[C/G]CTGTCCCCATGCCTT	80176
rs114187754	snp	C/T	0.00318978	0.0398085	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9292009	CCTCGGGCCAGGCAC[C/T]GTTTCCTCGCCTTTA	80176
rs114192199	snp	C/T	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9296996	ACAGGCTTAGGCTCT[C/T]GGGGCCTTTCTTGGA	80176
rs114198579	snp	A/G	0.0279526	0.114869	intron-variant	SPSB1	GRCh38.p7	1:9316310	GTTGGAGATGGGGGC[A/G]TCCCTTGGCATGCTA	80176
rs114205027	snp	C/G/T	0.0135079	0.0812644	intron-variant	SPSB1	GRCh38.p7	1:9327096	CATCTGCCGTCGTTT[C/G/T]GTGGGGAAGAGACTA	80176
rs114235733	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9327977	CACCAAAGTGCAAGC[C/T]GCTGACCTTGGATGG	80176
rs114267463	snp	A/G	0.0236746	0.106192	intron-variant	SPSB1	GRCh38.p7	1:9324976	GAGGCGCCTGTGAGC[A/G]GGTCAGTACTGGGTA	80176
rs114269106	snp	A/G	0.0107246	0.0724382	intron-variant	SPSB1	GRCh38.p7	1:9354231	GCCTCCCCTACCCCG[A/G]GTTCCTTTGGGTTCT	80176
rs114326013	snp	C/T	0.169061	0.236535	intron-variant	SPSB1	GRCh38.p7	1:9362192	CCACCCTCCCTCCCT[C/T]CCTTCCTTCCTTCCT	80176
rs114332584	snp	A/C	0.00795532	0.062565	intron-variant	SPSB1	GRCh38.p7	1:9300987	CTGCAGCACTATAGC[A/C]CCTTGCTGGGACACC	80176
rs114332845	snp	C/G	0.00478085	0.0486577	intron-variant	SPSB1	GRCh38.p7	1:9319460	TAGGATCTCAAAGTA[C/G]AGGGGTGGGATGAGA	80176
rs114335093	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9348998	GTGCATGTGTGTGTG[C/T]AGTGGTGGGGTATTC	80176
rs114361103	snp	C/T	0.0252325	0.109451	intron-variant	SPSB1	GRCh38.p7	1:9304917	GGTTCAAGCAATCCT[C/T]CCAAAGTGCTAGGAT	80176
rs114365151	snp	A/G	0.0539704	0.155153	intron-variant	SPSB1	GRCh38.p7	1:9318383	GCACAGCATTTCCAG[A/G]CTGCCTTGCGGACAG	80176
rs114376140	snp	C/G	0.0178098	0.0926698	intron-variant	SPSB1	GRCh38.p7	1:9326182	CCTTTCATTGGTTGA[C/G]GTTTTGGTGCTCATG	80176
rs114425842	snp	C/T	0.0260105	0.111035	intron-variant	SPSB1	GRCh38.p7	1:9358129	GTCCTCCTCCTGCTC[C/T]TCCTCCCCCACGTCA	80176
rs114447973	snp	A/G	0.00716266	0.059414	intron-variant	SPSB1	GRCh38.p7	1:9353515	CTCTGGAACCAGGGC[A/G]GCCCTCTAGGCTGCA	80176
rs114558831	snp	C/T	0.0399052	0.1355	intron-variant	SPSB1	GRCh38.p7	1:9319936	TGGGAGGACCATAGC[C/T]GGCCCCTGAGCTGGC	80176
rs114575891	snp	C/T	0.0861826	0.188849	intron-variant	SPSB1	GRCh38.p7	1:9320977	TTAAAATCTCCTTCC[C/T]GAGTCCCTGGCTGCC	80176
rs114591949	snp	C/G	0.0287284	0.116357	intron-variant	SPSB1	GRCh38.p7	1:9299937	TTACTTTACTCCAAC[C/G]TGGGCAACAGAGTAA	80176
rs114611408	snp	A/G	0.0517044	0.152246	intron-variant	SPSB1	GRCh38.p7	1:9293976	TTTATGTGCCTCTGA[A/G]TGTGTGTGTGAGTCT	80176
rs114655411	snp	C/T	0.0107246	0.0724382	intron-variant	SPSB1	GRCh38.p7	1:9311525	CTTTTCTGGAAAGAC[C/T]GATCGGGCTTAGAAA	80176
rs114709597	snp	C/G	0.225893	0.248835	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9292645	ACCCGAGCTTCGGGC[C/G]GGCAACACCAGGGCG	80176
rs114725568	snp	C/G	0.0256215	0.110247	intron-variant	SPSB1	GRCh38.p7	1:9344815	CTTCCTGAGTCCTCA[C/G]ATCCCTTCCCCGGTC	80176
rs114725575	snp	C/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9320793	TGTTTCTTGTTTCCT[C/T]GTGGGGGATTTTAAA	80176
rs114774166	snp	A/G	0.00953873	0.0683987	intron-variant	SPSB1	GRCh38.p7	1:9306959	TTTAAGTGGAATCTC[A/G]CTCTGTCATTCAGGC	80176
rs114778092	snp	G/T	0.0162398	0.0886349	intron-variant	SPSB1	GRCh38.p7	1:9330617	CGTTTGGGGGAGTAT[G/T]TTGGGTTTGCCTGTC	80176
rs114832327	snp	A/G	0.0138799	0.0821421	intron-variant	SPSB1	GRCh38.p7	1:9346581	GCATTTTGGGGGAAG[A/G]TGGGGTCTGCAGGGT	80176
rs114892223	snp	C/T	0.029116	0.117091	intron-variant	SPSB1	GRCh38.p7	1:9316611	ACGAAAGGCTGGGAG[C/T]GTTTTGCTACCTTAG	80176
rs114903103	snp	A/G	0.0240643	0.107019	intron-variant	SPSB1	GRCh38.p7	1:9331729	GATCCCACCAGCCAC[A/G]TTGGTACTTGCTCTC	80176
rs114913417	snp	C/T	0.0399052	0.1355	intron-variant	SPSB1	GRCh38.p7	1:9338523	CCCTGGCCACTCTCT[C/T]GCCAGCTCCGGCCTC	80176
rs114939004	snp	A/G	0.0260105	0.111035	intron-variant	SPSB1	GRCh38.p7	1:9317570	CTGCCTCCCAGGCTC[A/G]GGGATCCTCACACCT	80176
rs114973202	snp	C/G	0.00318978	0.0398085	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291984	TGGGTTCCAAGCTCT[C/G]GACAGCTGGCCTCGG	80176
rs114988625	snp	A/G	0.021333	0.101051	intron-variant	SPSB1	GRCh38.p7	1:9358829	TCATAGCTCCAGTAC[A/G]GTACACAGACCCCTG	80176
rs115042676	snp	A/G	0.00676609	0.0577691	intron-variant	SPSB1	GRCh38.p7	1:9309113	GAAGGCTGCAGAGCT[A/G]TGTAGCAGGGAGGGC	80176
rs115107389	snp	A/G	0.0168055	0.0901129	intron-variant	SPSB1	GRCh38.p7	1:9312889	GAGGCAGTGCGTGCC[A/G]ATTGTCCAAAGCCAG	80176
rs115111091	snp	A/G	0.0221141	0.102801	intron-variant	SPSB1	GRCh38.p7	1:9353535	TCTAGGCTGCAGAGG[A/G]GACACCTCAGCTCTG	80176
rs115298167	snp	C/T	0.0337553	0.125452	intron-variant	SPSB1	GRCh38.p7	1:9294683	TCATGGTAAAAGCGC[C/T]ATCCCTGGTGACTAA	80176
rs115315451	snp	C/T	0.0225045	0.103662	intron-variant	SPSB1	GRCh38.p7	1:9305486	TAGTTAGGTCCACAG[C/T]AGGTTCTTGGACACC	80176
rs115353938	snp	A/G	0.0456336	0.143994	intron-variant	SPSB1	GRCh38.p7	1:9323089	GGCCGCCCCTCCCCA[A/G]CTCCGGCCTTCGAGG	80176
rs115370015	snp	C/T	0.0520825	0.152737	intron-variant	SPSB1	GRCh38.p7	1:9351657	AAGGGTGGATCTGTG[C/T]GGCCACATTTTAAAA	80176
rs115370515	snp	A/G	0.0150606	0.0854603	intron-variant	SPSB1	GRCh38.p7	1:9340926	AGAGTGGGAAGGGGA[A/G]AAGACTGGTCTAGCT	80176
rs115375320	snp	A/G	0.0410537	0.137264	intron-variant	SPSB1	GRCh38.p7	1:9337596	TTCAGCTGTGAGTGC[A/G]GCGCCTCCAGCCTTG	80176
rs115395114	snp	C/T	0.0360663	0.129354	intron-variant	SPSB1	GRCh38.p7	1:9308108	TTCAGCTTTAGCAAG[C/T]TACTGTCTTAATTCC	80176
rs115461495	snp	A/G	0.00755907	0.0610114	intron-variant	SPSB1	GRCh38.p7	1:9344575	CAGGTGTTGAGAGGC[A/G]GCAGGAGGAGGGCAG	80176
rs115501445	snp	G/T	0.0263992	0.111815	intron-variant	SPSB1	GRCh38.p7	1:9311981	CCTCATGCAGATGAC[G/T]TTTTTGTCTTGGTGT	80176
rs115531303	snp	A/G	0.273587	0.248885	intron-variant	SPSB1	GRCh38.p7	1:9293454	ACCCGTCCCCCCTTT[A/G]GCCCGGGGAAAGCGG	80176
rs115560042	snp	C/T	0.00279162	0.0372561	intron-variant	SPSB1	GRCh38.p7	1:9326876	GGATGCAGCAGGGTG[C/T]TTGCTGCCAAGGGAG	80176
rs115575011	snp	A/G	0.0023933	0.0345097	downstream-variant-500B	SPSB1	GRCh38.p7	1:9369824	TGATTCTGTGCCTTC[A/G]TGAGCGCATCAGGTT	80176
rs115629115	snp	A/G	0.00676609	0.0577691	intron-variant	SPSB1	GRCh38.p7	1:9345425	AGGCTAGGCAGTGTC[A/G]GTGGTCCATAGTCCA	80176
rs115630078	snp	A/G	0.0501905	0.150254	intron-variant	SPSB1	GRCh38.p7	1:9361670	GGGGCCACAGGCCCC[A/G]TGCTCTGATTCCTCC	80176
rs115639204	snp	A/T	0.00676609	0.0577691	intron-variant	SPSB1	GRCh38.p7	1:9302184	TATGGTTTAAGAAGA[A/T]GCCAGTGGGTGCCTA	80176
rs115657883	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9302906	TAGGGACCCGCTAGC[A/G]AAATTGTTGCTTCCT	80176
rs115701864	snp	C/T	0.0119091	0.0762411	downstream-variant-500B	SPSB1	GRCh38.p7	1:9369662	CCTACCACCCCTTGG[C/T]AGAGGGTGGGATGCC	80176
rs115816350	snp	C/T	0.00676609	0.0577691	intron-variant	SPSB1	GRCh38.p7	1:9304457	TAATGCAGTTATGGT[C/T]GCCTTAAGAATCTGG	80176
rs115843159	snp	C/T	0.0225045	0.103662	intron-variant	SPSB1	GRCh38.p7	1:9295697	CCCCATGGTGTGTGC[C/T]GTGCTCCCTTCCTGC	80176
rs115877860	snp	A/G	0.00953873	0.0683987	intron-variant	SPSB1	GRCh38.p7	1:9315505	GACCTGGAGAGGCTC[A/G]AGTCACATGACGGGG	80176
rs115907745	snp	C/G	0.00914312	0.0669923	intron-variant	SPSB1	GRCh38.p7	1:9307825	CAGCAGTTCCCATTG[C/G]TATTACGGTGAATTT	80176
rs115911032	snp	C/T	0.00398564	0.0444627	intron-variant	SPSB1	GRCh38.p7	1:9322223	ATGCATCAGGCTGAG[C/T]AGAGTACCAGCATCG	80176
rs115917671	snp	A/G	1.65203e-05	0.002874	synonymous-codon	SPSB1	GRCh38.p7	1:9355978	GGAGCTCCAGGGTCT[A/G]GATTACTGCAAGCCC	80176
rs115964851	snp	C/T	0.0295035	0.117819	intron-variant	SPSB1	GRCh38.p7	1:9348413	TCCTGCCCCTCCAGG[C/T]TCCCTCAGCCTTCAG	80176
rs116031543	snp	A/G	0.00914312	0.0669923	intron-variant	SPSB1	GRCh38.p7	1:9316982	CCCCGTAGCAGGGCC[A/G]GGCCTCACCTTGGAT	80176
rs116041062	snp	A/G	0.0107246	0.0724382	intron-variant	SPSB1	GRCh38.p7	1:9363640	GGGGCTGCGGTGTCA[A/G]CCACTCAAAATAAGG	80176
rs116061445	snp	C/T	0.0209421	0.100162	intron-variant	SPSB1	GRCh38.p7	1:9322686	ACCACCTGCAGGTTC[C/T]ACTGTGGCTGGAATA	80176
rs116063121	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9333277	ATATGCATTTATCTC[A/C]TTTTTCAAGTCCACT	80176
rs116089991	snp	G/T	0.00438332	0.0466095	intron-variant	SPSB1	GRCh38.p7	1:9329483	GGGCATGGCCACCCA[G/T]CAGAAGTTAGTGCTG	80176
rs116092941	snp	C/T	0.0263992	0.111815	intron-variant	SPSB1	GRCh38.p7	1:9312943	AGACACACCTTTTCC[C/T]TCTGGCTTTAGAACA	80176
rs116222751	snp	C/T	0.00874735	0.0655527	intron-variant	SPSB1	GRCh38.p7	1:9311205	CATGCAGCCAGTATT[C/T]CCTGAATGCCCGCTC	80176
rs116243043	snp	A/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9326826	TTTAATCGGAAAGGC[A/T]TATTGCCTCTGAGTC	80176
rs116255862	snp	A/G	0.0189856	0.0955633	intron-variant	SPSB1	GRCh38.p7	1:9338784	GGTGGCGTGGGCCAC[A/G]ATTCTGCCTTCGCCC	80176
rs116283725	snp	C/G	0.00750679	0.0608033	intron-variant	SPSB1	GRCh38.p7	1:9367414	TGAACACCCACCCAA[C/G]CTGCGCTGACCTGCA	80176
rs116298920	snp	C/T	0.0263992	0.111815	intron-variant	SPSB1	GRCh38.p7	1:9348255	AACTTTTTTTAACCC[C/T]GGGCATCCCACAGCA	80176
rs116333149	snp	C/T	0.00755907	0.0610114	intron-variant	SPSB1	GRCh38.p7	1:9342763	CTACAGGTGCTGTCT[C/T]GGGGCAGCAAGGGCT	80176
rs116333290	snp	A/T	0.00517822	0.0506191	intron-variant	SPSB1	GRCh38.p7	1:9346272	TTGTTCCACATCCTG[A/T]ATTTCATTCTTTCCC	80176
rs116343896	snp	A/G	0.0287284	0.116357	intron-variant	SPSB1	GRCh38.p7	1:9343211	CCCTAAAAGAGGCTC[A/G]AGTCCCAAAACAGTT	80176
rs116349672	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9361787	AGTGGAGATGGCCAT[C/T]GCTGAGTGGGGAGAC	80176
rs116388432	snp	C/T	0.00358779	0.0422022	intron-variant	SPSB1	GRCh38.p7	1:9302083	ATCATGTGCAGGGAA[C/T]TGGCCGGTGAGCACG	80176
rs116425921	snp	G/T	0.00438332	0.0466095	intron-variant	SPSB1	GRCh38.p7	1:9343477	ATATTCCACTGAATG[G/T]GTATACCACAATTTG	80176
rs116480590	snp	A/C	0.00597247	0.0543191	intron-variant	SPSB1	GRCh38.p7	1:9325230	TCCCACCACCACCCC[A/C]CCCCCCCGCCCCGCC	80176
rs116481604	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9304216	CATACCATTGGTCCC[C/T]GGGGTCTTTGGCCCG	80176
rs116483489	snp	C/G	0.0425829	0.139564	intron-variant	SPSB1	GRCh38.p7	1:9354299	ACCCAGCGTGACTCT[C/G]TCCCGGCAGCCAAGG	80176
rs116533116	snp	A/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9306343	GCTGGAGTGGGAGGG[A/T]TAACCAGTTTTCCTT	80176
rs116605840	snp	A/C/T	0.00637247	0.0561273	intron-variant	SPSB1	GRCh38.p7	1:9299464	GGCAACACAGTGAGA[A/C/T]GTCATCTCTCTCTCT	80176
rs116610624	snp	A/G	0.0283406	0.115616	intron-variant	SPSB1	GRCh38.p7	1:9354230	AGCCTCCCCTACCCC[A/G]GGTTCCTTTGGGTTC	80176
rs116645411	snp	A/G	0.00358779	0.0422022	intron-variant	SPSB1	GRCh38.p7	1:9358966	GCTCTGCATGAGATG[A/G]GAGGTTGGATGCTTT	80176
rs116684185	snp	C/T	0.0162398	0.0886349	intron-variant	SPSB1	GRCh38.p7	1:9310383	TTTCTAAGGGATGAG[C/T]TCCTGGATAGATCAA	80176
rs116730116	snp	A/G	0.021333	0.101051	intron-variant	SPSB1	GRCh38.p7	1:9317995	GAGGAAGCTGGGTGG[A/G]CAGTCGCAGGTTTGG	80176
rs116791428	snp	A/G	0.0115144	0.0749975	intron-variant	SPSB1	GRCh38.p7	1:9305950	AAATGAGTGCAGAGA[A/G]GCAGGAGGGCCCACA	80176
rs116824634	snp	A/C	0.0221141	0.102801	intron-variant	SPSB1	GRCh38.p7	1:9320716	ACTGCACCCCGGGCT[A/C]GCCTCTCTCGGCTCT	80176
rs117001661	snp	G/T	0.00795532	0.062565	intron-variant	SPSB1	GRCh38.p7	1:9360188	GAGGGCTGAGGCTGA[G/T]CCCTGCTTAGAGGCC	80176
rs117359473	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9294269	GTCCACACGTGTCTC[A/T]GTGTCTGTCTCTGTG	80176
rs117363470	snp	C/T	0.0142736	0.0832652	intron-variant	SPSB1	GRCh38.p7	1:9302136	TGCTAAGTGGAACTA[C/T]GGTCTTGTTATTGCC	80176
rs117529410	snp	A/G	0.00795532	0.062565	intron-variant	SPSB1	GRCh38.p7	1:9354937	GGCCAGAGAGGGAAC[A/G]AGGCATCCTAGCATC	80176
rs117773034	snp	A/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9337313	CCCTGAAGTCCCTCT[A/G]AGAGGCCAAGGACGG	80176
rs117912845	snp	A/G	0.00676609	0.0577691	intron-variant	SPSB1	GRCh38.p7	1:9346814	TGCTGTGCAGCTGCC[A/G]CCTGGCTGGGTATGG	80176
rs117925885	snp	C/T	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9304861	AATTTCTCACAAAGA[C/T]GGTGTCTCCCTATGT	80176
rs117956834	snp	C/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9293944	TGTGTGAGTGTGTCT[C/G]TAAGTGCATCTGTGT	80176
rs117990778	snp	A/G	0.00517822	0.0506191	intron-variant	SPSB1	GRCh38.p7	1:9338334	CCAGGGAGGAGGTTC[A/G]TGACTGTATGGGGGC	80176
rs118005243	snp	A/G	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9303128	GACTACCAAGGGGAA[A/G]TTGATCTGGACTGCT	80176
rs118020816	snp	C/T	0.021333	0.101051	intron-variant	SPSB1	GRCh38.p7	1:9362351	GATCTCAGGCGTCCT[C/T]CCCCAGTTGACAAGG	80176
rs118161917	snp	G/T	0.00438332	0.0466095	intron-variant	SPSB1	GRCh38.p7	1:9336810	ACTGCTCCCTGGAAA[G/T]AGGGGGACACTAGCC	80176
rs137867479	in-del	-/AGACCATGTTTCT	0.0551013	0.156571	intron-variant	SPSB1	GRCh38.p7	1:9337019	TTGGCATCTGGCTGC[-/AGACCATGTTTCT]AGCTCTCTCTGGCAT	80176
rs137982966	snp	C/G	0.0111196	0.0737302	intron-variant	SPSB1	GRCh38.p7	1:9331880	GAGCTTCTTTTCCTA[C/G]AAGTTTACTTACTGT	80176
rs138006573	snp	C/T	0.00795532	0.062565	intron-variant	SPSB1	GRCh38.p7	1:9362630	CTCGTTCACTCAGCC[C/T]GTGAACTGGGCACAG	80176
rs138029782	snp	C/T	0.00438332	0.0466095	intron-variant	SPSB1	GRCh38.p7	1:9305177	ATATTCTGCTGACCC[C/T]GTCTCACACTCTTCA	80176
rs138044973	snp	C/T	0.00318978	0.0398085	intron-variant	SPSB1	GRCh38.p7	1:9296889	GAAACCTTTGGGAAG[C/T]TGCCTGTTTGCTTTG	80176
rs138067261	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9310929	ATATATAAATTATAC[A/G]TACATGTCAGGGTTC	80176
rs138110257	snp	A/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9301627	CCTAGGTGGATTCTC[A/G]TCAGCCTCTTTCCCT	80176
rs138111075	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9339451	GAGGTGCTCTGAGAC[A/G]GCTGCAGTGGAGGCC	80176
rs138111636	snp	C/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9366527	ATTCAGATCCCAGCC[C/T]TGAACCTTGGCACAC	80176
rs138124874	snp	A/G	0.00358779	0.0422022	intron-variant	SPSB1	GRCh38.p7	1:9329236	GGTTGAGGGTTTGTG[A/G]GTGGGGGGAAATGCA	80176
rs138163681	snp	A/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9343355	GAAAGGGAATCGTAC[A/G]ATGTGTGACCTTTTA	80176
rs138219792	in-del	-/TG	0.00953873	0.0683987	intron-variant	SPSB1	GRCh38.p7	1:9332013	TGAGTGTTGAAAATA[-/TG]TGACTCTTTTGTACG	80176
rs138248053	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9329704	TTTCAAAAACAACAA[A/C]AAAAAAAAAAAAAAA	80176
rs138269351	snp	C/T	0.000538423	0.0163988	synonymous-codon	SPSB1	GRCh38.p7	1:9356140	TCCGGTGGCCCAGAG[C/T]ACGGACGCTATCAGG	80176
rs138274004	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9319645	GCTGGTATTCCGTTC[C/T]GGCTGGTGCAGAGGA	80176
rs138375245	snp	A/G	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9350356	CATTGGTTTGTTGTG[A/G]GGCTTGGCTGAGACA	80176
rs138386258	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9358381	TCCTGGAAGAGGTGG[A/G]TGACCAGGCCTGCAG	80176
rs138388044	in-del	-/GAAT			intron-variant	SPSB1	GRCh38.p7	1:9298408	AATGAATGAGTGAAC[-/GAAT]GAATGAATAAGTGAA	80176
rs138434233	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9311526	TTTTCTGGAAAGACC[A/G]ATCGGGCTTAGAAAT	80176
rs138496270	snp	A/G	0.0923359	0.194016	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291016	GTGCAGTGGTGCGAT[A/G]TCGGCTCACTGCAAC	80176
rs138497370	snp	C/G	0.021333	0.101051	intron-variant	SPSB1	GRCh38.p7	1:9358022	AGGCAAGAGGCAGAG[C/G]GGGGTGAGGCCCCCC	80176
rs138497868	snp	C/T	0.000153988	0.00877328	missense	SPSB1	GRCh38.p7	1:9367480	ATGGATTTGTGCCGT[C/T]GCTCGGTGCGCCTGG	80176
rs138549133	snp	C/T	0.00676609	0.0577691	intron-variant	SPSB1	GRCh38.p7	1:9304330	CAGCTTGCAGATGGC[C/T]TGTAGTGGGACTCAG	80176
rs138554740	in-del	-/GAGGTCAGGGACTA	0.0103295	0.0711199	intron-variant	SPSB1	GRCh38.p7	1:9345739	CATTTTGGGTCTTTT[-/GAGGTCAGGGACTA]GAGCTCTGGACCGTG	80176
rs138628912	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9347565	TTTTTAAATTCTGTT[C/G]TTTCAGAAACGGCAT	80176
rs138669166	snp	C/T	0.00318978	0.0398085	intron-variant	SPSB1	GRCh38.p7	1:9333093	CAAGAATCAGCCTCC[C/T]AGGTGCACACTCCAT	80176
rs138743235	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9305405	TGGGCAGCCCAGTGA[C/T]CTGTGGGCTCCAGGA	80176
rs138767151	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9328491	ATGCCTTAAGAATCC[A/G]TCAAGGCCACTTCGG	80176
rs138846242	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9363255	GTTTATGTACTTGAG[A/G]ACCCAGAGAAGAGAC	80176
rs138898717	snp	A/G	7.23406e-05	0.00601374	utr-variant-5-prime	SPSB1	GRCh38.p7	1:9355865	TTTGCCTTGGGAGTC[A/G]GTAAGAAGGTGAAGC	80176
rs138940191	in-del	-/GTGA			intron-variant	SPSB1	GRCh38.p7	1:9294270	CCACACGTGTCTCTG[-/GTGA]TGTCTGTCTCTGTGT	80176
rs138999340	snp	A/G	0.00835141	0.0640778	intron-variant	SPSB1	GRCh38.p7	1:9319937	GGGAGGACCATAGCC[A/G]GCCCCTGAGCTGGCC	80176
rs139033256	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9322889	ACCCGCCCGGACGCT[C/T]TTCTCAGCCCCTTTT	80176
rs139181482	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9347821	TTGCACATGGACAGG[A/G]ACTGCCTCGTTGTAC	80176
rs139194880	in-del	-/GA			intron-variant	SPSB1	GRCh38.p7	1:9309262	GTGTGCTCCCCTGCG[-/GA]GAGAGAGAGAGAGAG	80176
rs139261599	snp	C/T	0.00636936	0.0560724	intron-variant	SPSB1	GRCh38.p7	1:9325490	GGAAGGTGGTGTGGG[C/T]GACCCTAGGCCCTGC	80176
rs139331489	snp	C/T	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9340201	AGGAGACAGACTCTC[C/T]TTGGGCAGGCTTTCT	80176
rs139337729	snp	A/G	0.00398564	0.0444627	intron-variant	SPSB1	GRCh38.p7	1:9367076	GGATCGCCTGGGTTC[A/G]AATCCTAGCTGCATC	80176
rs139462257	snp	A/G	0.00279162	0.0372561	intron-variant	SPSB1	GRCh38.p7	1:9364210	CCCGGGAGGGAGCTC[A/G]GGGCAGCCCAGACCC	80176
rs139527079	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9302151	CGGTCTTGTTATTGC[C/T]TTTATTTGGAAATTA	80176
rs139701593	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9293970	TGTGTATTTATGTGC[C/T]TCTGAGTGTGTGTGT	80176
rs139704937	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9360308	GGTCAAGTACATGGA[C/T]GGCTGAGAACCGTCC	80176
rs139752168	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9321399	CCCATTCTTGGGAGA[C/G]AGCGGATCCTGTGTG	80176
rs139802796	in-del	-/GTTTTTTTTT			intron-variant	SPSB1	GRCh38.p7	1:9349781	ACCGTTTTATGGCTG[-/GTTTTTTTTT]TTTTTCTCTCTTGAC	80176
rs139808151	in-del	-/ACTG	0.00405736	0.0448577	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9367622	ACCTGGTGCCAACTC[-/ACTG]AGCCGCCTGCCGCTG	80176
rs139816488	snp	C/T	0.00318978	0.0398085	intron-variant	SPSB1	GRCh38.p7	1:9316703	TCCTGTGGCGCGGCA[C/T]GGGCCTTCGTCAGGA	80176
rs139818122	snp	C/T	0.00716266	0.059414	intron-variant	SPSB1	GRCh38.p7	1:9306439	ACCGGGGTCTGTCTA[C/T]AGTGGGGTCAGTGAC	80176
rs139840514	in-del	-/C	0.0123036	0.0774623	intron-variant	SPSB1	GRCh38.p7	1:9358822	TTATGTATCATAGCT[-/C]CAGTACAGTACACAG	80176
rs139856142	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9353382	GTGTCCCTCTGCAGC[A/G]CCATGGAGGGAGTCC	80176
rs139909114	snp	A/G	3.30316e-05	0.00406383	missense	SPSB1	GRCh38.p7	1:9356328	GCTGGGACTTGGGGC[A/G]CAACCGGCTCTACCA	80176
rs140026158	in-del	-/TC	0.0314385	0.121371	intron-variant	SPSB1	GRCh38.p7	1:9307622	GGTGGGATGGAAGAG[-/TC]TGATCCAAACAGCTT	80176
rs140033787	snp	A/G	0.00318978	0.0398085	intron-variant	SPSB1	GRCh38.p7	1:9333843	TTTCCTCTCCAGCGC[A/G]GCTCCGGGGAAAACA	80176
rs140045808	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9307766	TCTTTTCCCGTTGAT[C/T]TATTAAAAATGACAC	80176
rs140073340	snp	A/G	0.0103295	0.0711199	intron-variant	SPSB1	GRCh38.p7	1:9366973	GGGGGTGCGTGCCAG[A/G]AAGAGCTGGCTCCCA	80176
rs140089434	snp	A/T	0.0146672	0.084371	intron-variant	SPSB1	GRCh38.p7	1:9306682	AGCACCATTTGCCAC[A/T]AAAGAGGAGCGAGGA	80176
rs140129567	snp	C/T	0.00398564	0.0444627	intron-variant	SPSB1	GRCh38.p7	1:9362434	GTAGAGGAAAACACA[C/T]ACACATCCTATGATG	80176
rs140155801	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9361542	CCTGCATGCCAGGCA[A/G]AACCCCCCCGCAGCA	80176
rs140221358	in-del	-/TGGATGGA			intron-variant	SPSB1	GRCh38.p7	1:9357090	GGATGGATGGGTGGG[-/TGGATGGA]TGGATGGATGGATGA	80176
rs140247394	snp	C/T	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9310520	CAACATGGTGAAACC[C/T]CGTCTCTACTAAAAA	80176
rs140283035	snp	A/C	0.00010367	0.0071989	missense	SPSB1	GRCh38.p7	1:9355931	ATCAAGACTGTGGAC[A/C]TGAGGGACCCCACGT	80176
rs140283959	snp	A/G	0.00398564	0.0444627	intron-variant	SPSB1	GRCh38.p7	1:9345765	CTAGAGCTCTGGACC[A/G]TGTGGGATTTTCTCT	80176
rs140319727	in-del	-/AC			intron-variant	SPSB1	GRCh38.p7	1:9350102	ACGCCTCACATATCT[-/AC]ACACACACACACACC	80176
rs140357559	snp	C/T	0.00914312	0.0669923	intron-variant	SPSB1	GRCh38.p7	1:9343233	AAAACAGTTTCATCA[C/T]CCCTAAAAGAAACCT	80176
rs140378808	snp	A/G	0.00953873	0.0683987	intron-variant	SPSB1	GRCh38.p7	1:9324034	GCCCAAACTCGGGCC[A/G]CAGAACCCCTCCTCA	80176
rs140386948	snp	A/T	0.00438332	0.0466095	intron-variant	SPSB1	GRCh38.p7	1:9349607	CCTCAGGAGGAAGCT[A/T]TCCACGGGACATGTC	80176
rs140404484	in-del	-/G	0.00318978	0.0398085	intron-variant	SPSB1	GRCh38.p7	1:9295246	TGTGTGTGTGTGCGC[-/G]CGTGCGGTTGGGGAG	80176
rs140523406	snp	A/G	0.00398564	0.0444627	intron-variant	SPSB1	GRCh38.p7	1:9320857	CCTGCGCCGGGTTTA[A/G]CAGGATGGAGTTAGA	80176
rs140563806	snp	A/G	0.00398564	0.0444627	intron-variant	SPSB1	GRCh38.p7	1:9330771	TTAACCATTTAAGAC[A/G]TGCAGTTCAGTAGCG	80176
rs140564804	snp	G/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9357770	GTGTGGGAGGTGAAG[G/T]CTCCATGGCTGCCCA	80176
rs140636579	snp	A/G	0.000577105	0.016977	synonymous-codon	SPSB1	GRCh38.p7	1:9356014	GCTGGATCTGCTACT[A/G]GACATGCCCCCTGTG	80176
rs140643910	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9327160	GGGGGTCCCAGGATG[A/G]CCCTCTAAGCCCACG	80176
rs140655442	snp	A/G	0.00318978	0.0398085	intron-variant	SPSB1	GRCh38.p7	1:9342718	CCGAGATGCAGGCAC[A/G]CATCCCGGACTCCTC	80176
rs140677263	snp	A/G	0.0376037	0.131863	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9290971	TTCTTTTTTTTTGAG[A/G]TGGAGTCTCGCTCTG	80176
rs140737992	snp	A/C	0.00953873	0.0683987	intron-variant	SPSB1	GRCh38.p7	1:9327925	CTAGATTTAAGAGGA[A/C]GGGCCCTAACGGGGC	80176
rs140879125	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9314998	AAGTCAAGAATCCAG[A/G]CTTTTTAAGATGTTG	80176
rs140887187	snp	A/G	0.0402882	0.136092	intron-variant	SPSB1	GRCh38.p7	1:9310175	GGCCACAGAGTCTAG[A/G]GGCCATCTGTGATGA	80176
rs140910968	in-del	-/GTGA			intron-variant	SPSB1	GRCh38.p7	1:9294104	GTCTGTGTGTCTTTG[-/GTGA]TGTGTGTCTGTGTGT	80176
rs140967617	snp	C/T	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9346620	TAATTGAAACACCAT[C/T]GGGGGGTTGCCGGCA	80176
rs140989855	snp	C/G	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9355228	GTGAATTGGTGGTGC[C/G]TCTGCTGGAGGTAGC	80176
rs141009248	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9307388	ACCCCATCCACATTC[A/G]GCGTCACCTCCCATC	80176
rs141017970	snp	A/G	0.00478085	0.0486577	intron-variant	SPSB1	GRCh38.p7	1:9335240	GGCACAGTGGCTCAC[A/G]CCTGTAATTCTTGCA	80176
rs141031530	snp	G/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9349459	AGCTGAGCTCAACCA[G/T]AGAGGCCAAGGGACG	80176
rs141033487	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9308163	ATGTCAGGCCCAAAG[A/G]GGGTGGACTGCCTCT	80176
rs141051718	in-del	-/TG	0.155656	0.231515	intron-variant	SPSB1	GRCh38.p7	1:9331168	CGTCTTTTTAATTGC[-/TG]TGTGTAACAACGGTT	80176
rs141052278	snp	A/C	0.0566069	0.158427	intron-variant	SPSB1	GRCh38.p7	1:9299734	TTCACCCGCCTTGGC[A/C]TCCCAAAGTTCTGGG	80176
rs141080108	snp	C/T	0.00318978	0.0398085	intron-variant	SPSB1	GRCh38.p7	1:9331658	TATGGGCTCACGCAC[C/T]AGGGGTGGAATTGTT	80176
rs141090917	in-del	-/CAAGGC			intron-variant	SPSB1	GRCh38.p7	1:9340422	TAGTGCATGTCAAGG[-/CAAGGC]CAAGGCGTTGTGTTA	80176
rs141148308	snp	A/C	0.00318978	0.0398085	intron-variant	SPSB1	GRCh38.p7	1:9335650	TACAAAAACTAAAAA[A/C]CTAGCTGAGCATGGT	80176
rs141161901	snp	A/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9296194	TCACGGTGCGTGCGA[A/G]TACTGGCTCTGATCT	80176
rs141205290	snp	A/G	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9356905	ATAATGGATGGATGC[A/G]TGTATAATGAATTGA	80176
rs141223867	snp	C/T	0	0	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9368608	TTGCTTTTGCTTTTC[C/T]AGCTGAGATTTCCCA	80176
rs141240826	snp	A/G	0.00795532	0.062565	intron-variant	SPSB1	GRCh38.p7	1:9338653	TCTGGGAAGGGAATC[A/G]TGCTGGCTTCACCTT	80176
rs141274983	snp	C/T	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9301308	CCAGCCTGAGCAACA[C/T]AGTGAGACTCCCCGC	80176
rs141297641	in-del	-/TG			intron-variant	SPSB1	GRCh38.p7	1:9348962	TCACTCGTGCAAGAA[-/TG]TGTGTGTGTGTGTGT	80176
rs141328316	snp	A/G	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9361823	GCCTGGCCTGACCCC[A/G]GGCCTGCCCGCCACC	80176
rs141360762	snp	C/T	0.0197687	0.0974348	intron-variant	SPSB1	GRCh38.p7	1:9364950	TCCACCTCCCAGGTT[C/T]AAGTGATTCTCCTGC	80176
rs141391723	snp	A/G	0.00914312	0.0669923	intron-variant	SPSB1	GRCh38.p7	1:9309219	GTTCCTGAGATGTGC[A/G]GATAAGCTAGATCCC	80176
rs141500134	snp	C/T	0.00953873	0.0683987	intron-variant	SPSB1	GRCh38.p7	1:9350036	ACACACATGAAGACA[C/T]ACCACACACATATAC	80176
rs141503915	snp	A/G	0.00478085	0.0486577	intron-variant	SPSB1	GRCh38.p7	1:9312444	TATTATGCACACGCC[A/G]CGCAGTTCGCCTATT	80176
rs141528780	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9361156	TGGATCTGTCATTTT[C/T]TTTTTTTTTTTTTTT	80176
rs141558790	snp	A/G	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9320176	TCCTCCTAAATTTGC[A/G]TGGCAGAAACTTCCT	80176
rs141559946	in-del	-/GT	0.0123036	0.0774623	intron-variant	SPSB1	GRCh38.p7	1:9359410	TCTTGTGTCTTAGGA[-/GT]GTCGTTCTGCGGCTG	80176
rs141576098	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9355067	AATCCCGGGGGTCGG[A/G]GGATGAGCCCCCCTT	80176
rs141578903	snp	C/G	0.00438332	0.0466095	intron-variant	SPSB1	GRCh38.p7	1:9351351	TGTGGTGACCAGGAA[C/G]ACAGGAGAACAGTGA	80176
rs141685667	snp	A/G	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9320547	TAGTGGCCTCGCTCC[A/G]TGCATCTAAGTTGTT	80176
rs141716941	snp	G/T	0.000798403	0.0199641	downstream-variant-500B	SPSB1	GRCh38.p7	1:9369865	GTTGTAGAACTTGAG[G/T]TGACCGTGGGCTTTT	80176
rs141840892	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9300091	ATTTACATGTCAAGC[A/G]ATGGGAAATAAATTC	80176
rs141905831	snp	C/T	0.00517822	0.0506191	intron-variant	SPSB1	GRCh38.p7	1:9303707	GCAGGATAGTAGTGT[C/T]ACGATAGGTGGAACT	80176
rs141911800	snp	A/G/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9300490	CCCTGTAGATGAATC[A/G/T]CAGTACAGGCCTTGG	80176

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