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
rs141912318	in-del	-/CAGATCTCGG			intron-variant	SPSB1	GRCh38.p7	1:9329768	GTCCAGGAGACTTCC[-/CAGATCTCGG]CATCGGACACATGGC	80176
rs141929420	snp	A/G	0.00517822	0.0506191	intron-variant	SPSB1	GRCh38.p7	1:9365693	CAGTAATTGATTTTC[A/G]TATATTTGAGACACA	80176
rs141986255	snp	A/G	0.00478085	0.0486577	intron-variant	SPSB1	GRCh38.p7	1:9339592	TTCTTAAGGACTAGC[A/G]GGGCTGGTGTGGCCA	80176
rs141989891	snp	C/T	0.0103295	0.0711199	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9367682	CGGCATCCGTAGCCA[C/T]GGACAGAGGTCCCTG	80176
rs141993039	in-del	-/T	0.402491	0.198107	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9369206	GACGGTTTTTTTTTT[-/T]CGGGGCAGGGGACCT	80176
rs142004796	snp	C/T	0.0387552	0.1337	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291096	CTGGGATCGCAGGCA[C/T]GTACCACCACACCCA	80176
rs142044518	in-del	-/TTG			intron-variant	SPSB1	GRCh38.p7	1:9364830	TTTTTTGTTGTTGTT[-/TTG]TTGTTGTTGTTGTTG	80176
rs142050992	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9345313	CTTTTCTTGGAGATG[C/G]CCGTGGGGCTGCTTT	80176
rs142083895	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9307731	CCTCTTGCAGCCAGC[A/G]ATCTTGTTACTTATT	80176
rs142154324	snp	A/G	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9349481	CAAGGGACGTGGAGC[A/G]TGAGAGGCTGAGGCC	80176
rs142217568	snp	A/C/T	0.00637415	0.0561569	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9292117	TTGTTTCGGCTCCCC[A/C/T]AGAAAGGCTAACTCC	80176
rs142228148	in-del	-/T	0.0232847	0.105357	intron-variant	SPSB1	GRCh38.p7	1:9326195	AGGTTTTGGTGCTCA[-/T]TGAGAAGACTTCTTC	80176
rs142244876	snp	C/T	0.00517822	0.0506191	intron-variant	SPSB1	GRCh38.p7	1:9323092	CGCCCCTCCCCAGCT[C/T]CGGCCTTCGAGGACT	80176
rs142293414	snp	C/T	0.00318978	0.0398085	intron-variant	SPSB1	GRCh38.p7	1:9363902	GATGAGGTTTTGCCA[C/T]ACTGGCCAGGCTGGT	80176
rs142321670	snp	C/T	0.00993419	0.0697739	intron-variant	SPSB1	GRCh38.p7	1:9315945	CGGGTTTCACGCGTG[C/T]GGCTCCGGGCATCCT	80176
rs142352924	in-del	-/G			intron-variant	SPSB1	GRCh38.p7	1:9330853	CTGTGTCCAGCGGCT[-/G]GTGCCATTTTGCGTT	80176
rs142353647	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9318712	GGTTGTTCTTCTGTC[C/T]ATTCAGCAATTCGGG	80176
rs142384909	snp	C/T	1.78191e-05	0.00298484	synonymous-codon	SPSB1	GRCh38.p7	1:9356581	CTACTTGAACGGACT[C/T]GATCGTAAGTGTCTC	80176
rs142421748	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9303247	TGGGAAATTACAAGG[A/G]TACAATCCAGGCAGG	80176
rs142429325	snp	A/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9366997	GCTCCCATGTGTTCC[A/G]ACCGACAGGCCCCAA	80176
rs142495682	snp	A/T	0.0209421	0.100162	intron-variant	SPSB1	GRCh38.p7	1:9310025	TTCTGGCTGGGGTAG[A/T]GTTGCCTGTTGCCCT	80176
rs142518224	snp	A/G	0.00318978	0.0398085	intron-variant	SPSB1	GRCh38.p7	1:9305230	TGGCCCGTTCCTACC[A/G]GCTGGCCCATACCCT	80176
rs142600576	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9314895	GCAGGGAGAGGACTG[C/T]GGCAAAGGAGAACAG	80176
rs142661774	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9301658	GGCCACCCCTGTCAT[C/T]GCCTGGTGGGCTCAG	80176
rs142700342	snp	A/G	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9354581	ACTTTGGGAGGCCAA[A/G]CCGGGTGGATCACCT	80176
rs142728049	snp	A/G	3.47705e-05	0.00416942	synonymous-codon	SPSB1	GRCh38.p7	1:9367530	GGGGGAGATCCACAC[A/G]CTGCCGCTGCCGGCT	80176
rs142734600	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9366956	TTCCTGAAGCTAGTG[C/T]TGGGGGTGCGTGCCA	80176
rs142749939	snp	C/T	0.00636936	0.0560724	intron-variant	SPSB1	GRCh38.p7	1:9328504	CCGTCAAGGCCACTT[C/T]GGGGGAAGAGCTGAT	80176
rs142791565	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9363545	CTCTCACCTCCCCAA[A/G]CCCATTTCCCTATCT	80176
rs142792121	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9306259	CTGGGCCTTCCTAGC[C/T]GCGTCCTGCAGCAGT	80176
rs142823263	snp	A/T	0.00438332	0.0466095	intron-variant	SPSB1	GRCh38.p7	1:9366455	AGGGTTTGCCATGTC[A/T]TCCTTTGCAGCATGG	80176
rs142826416	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9329981	GCGGGTTCAGAGTGG[C/T]CCAGGAGCAGGTGAC	80176
rs142914039	snp	C/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9319764	TACTACAGGGAAGTC[C/G]GCCTGGGGTGGCGGG	80176
rs143052261	snp	C/T	0.030665	0.119967	intron-variant	SPSB1	GRCh38.p7	1:9331419	CACTGTAACCTCTGC[C/T]TCCTGGGTTCAAGCG	80176
rs143053972	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9358188	GGGGTGGTTAGGCAT[A/G]CGCAAACGCTTACAC	80176
rs143056259	snp	A/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9316567	GAGGAGGGGGGGGCT[A/G]ATCGAAGCGGGTTCA	80176
rs143105028	snp	A/G	0.0263992	0.111815	intron-variant	SPSB1	GRCh38.p7	1:9348137	TTTAGTAGAGATGGG[A/G]TTTCACTATGTTGGC	80176
rs143156131	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9338048	GCTGGGGTGCAGGGA[A/G]GAGGGAGCAGGTTTG	80176
rs143160541	snp	A/G	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9343617	CACTCTAAACACAGC[A/G]ACATTTTCATTTCTC	80176
rs143183883	in-del	-/CGCGCCC	0.25045	0.25	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9292725	CCAGCGCCGGGCTGA[-/CGCGCCC]CGCGCCCCGCGCCCC	80176
rs143223152	snp	C/T	1.66167e-05	0.00288237	synonymous-codon	SPSB1	GRCh38.p7	1:9356083	CGACCGATCGCTCAA[C/T]GTCTTTGTGAAGGAG	80176
rs143259262	in-del	-/TGAA			intron-variant	SPSB1	GRCh38.p7	1:9357133	GGATGGATGGATGAG[-/TGAA]TGGATGGATGGATGG	80176
rs143272581	snp	A/G	0.00874735	0.0655527	intron-variant	SPSB1	GRCh38.p7	1:9314045	GCCAGGTGTGGCGGC[A/G]GGCACTTGTTATCCC	80176
rs143298864	snp	A/C	0.00318978	0.0398085	intron-variant	SPSB1	GRCh38.p7	1:9357394	TAATAAGTAGGTGGT[A/C]TTTGTTTCTCTGGGT	80176
rs143398862	snp	C/G	0.0298908	0.118541	intron-variant	SPSB1	GRCh38.p7	1:9295731	TGCCCCTCCTCCTGG[C/G]TGGATGGAAACTTGC	80176
rs143472419	snp	A/C/G	0.0103295	0.0711199	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9368702	GGGTCTCCATTCCCC[A/C/G]AGAAGCCGGGGGCAG	80176
rs143513449	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9297255	GCGTCTCTTGGAAAA[C/T]TAGGGAGGCATTGGG	80176
rs143527887	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9363114	CTGGGCATTTTTTCA[C/T]GGCACGAAGCCCACG	80176
rs143561029	snp	C/G	0.00318978	0.0398085	intron-variant	SPSB1	GRCh38.p7	1:9333871	ACAGCTCAAGGTAGA[C/G]AGGACCTGGCTGTTG	80176
rs143629299	snp	C/T	0.0267878	0.112589	intron-variant	SPSB1	GRCh38.p7	1:9299522	TTTGCTCTTGTTGCC[C/T]AGGCTGGAGTGCAAT	80176
rs143656102	snp	A/G	0.00557542	0.0525036	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291631	TGCTCTGTTGCCCGG[A/G]CTGCTCTTGAACTCC	80176
rs143671771	snp	A/G	0.0111196	0.0737302	intron-variant	SPSB1	GRCh38.p7	1:9359357	TGCCAGCCTCAACCC[A/G]CTTAACCCGACACCT	80176
rs143705280	in-del	-/CA	0.0573587	0.15934	intron-variant	SPSB1	GRCh38.p7	1:9357854	TGTACGGCCCTCTCT[-/CA]GAGTTCCTTGCCTGC	80176
rs143714382	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9322331	AAAGTCTCTCAGGTT[A/G]TAGCCGGTAAGGGCA	80176
rs143793491	snp	A/G	0.0240643	0.107019	intron-variant	SPSB1	GRCh38.p7	1:9365317	CGATGAGGTCTCCCT[A/G]TGTTGCTCAGGCTGG	80176
rs143828613	snp	C/G	0.00318978	0.0398085	intron-variant	SPSB1	GRCh38.p7	1:9327411	AACAGGATAGTAGCT[C/G]CTGGAAATGAGGTTC	80176
rs143925282	in-del	-/TGAATGAATAAGTGAACGAATGAATGAATAAG			intron-variant	SPSB1	GRCh38.p7	1:9298411	GAATGAGTGAACGAA[lengthTooLong]TGAATGAATAAGTGA	80176
rs143964206	snp	A/C	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9324020	AGCTGTCCTTGATGG[A/C]CCAAACTCGGGCCGC	80176
rs143964843	snp	C/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9348637	AACTGGAGGGATTTG[C/T]GAGGTTCTTTTCTTC	80176
rs143971636	in-del	-/ATGG			intron-variant	SPSB1	GRCh38.p7	1:9357220	TGGATCAGTGAATGA[-/ATGG]ATGGATGGATGGATG	80176
rs143973383	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9353049	CTCCCAGGGAGCTGA[A/C]CTCTGTGCCCACAGG	80176
rs144032916	snp	A/G	0.00517822	0.0506191	intron-variant	SPSB1	GRCh38.p7	1:9309363	CTCTCTGTCACCCAG[A/G]CTGGAGTGCAGTGGT	80176
rs144047874	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9349345	ATATTGGTGACGTGT[C/T]CTCTCCCTTTATCCC	80176
rs144099758	snp	A/T	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9366661	CCACTGCAACCTCCA[A/T]CTCCCAGGTTCAAGC	80176
rs144122412	snp	A/G	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9345915	GGTGAGGGGTGGAGG[A/G]TGGTAACCACGTGTC	80176
rs144162677	snp	A/G	0.00676609	0.0577691	intron-variant	SPSB1	GRCh38.p7	1:9329432	CAGGTGAGAGGATCC[A/G]AGGAAGGGAGTAGGG	80176
rs144184760	snp	A/G	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9302558	ATGCTCTTCTCCTGC[A/G]CTTGGATGTCAGAAC	80176
rs144296890	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9302648	CCTGGGACTGGGAAT[A/G]ACCACGTTCCCCACC	80176
rs144304499	snp	C/G	0.00358779	0.0422022	intron-variant	SPSB1	GRCh38.p7	1:9364315	CTCTGTGCAGAAGAC[C/G]TACTCCCGACAGCCA	80176
rs144334629	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9351182	ATTGATTTACATATT[A/G]TCCGGAGAGCCTTAA	80176
rs144422263	snp	C/T	0.000334666	0.0129314	synonymous-codon	SPSB1	GRCh38.p7	1:9356272	CCCCCTGCACTCTGT[C/T]GGGTACACAACCCTC	80176
rs144440810	snp	C/T	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9349074	CGTGTCATCTGGTGT[C/T]CCCGCAGGTAGCCCC	80176
rs144506644	snp	A/G	0.00358779	0.0422022	intron-variant	SPSB1	GRCh38.p7	1:9359264	CGTTCTTGGGACACC[A/G]AGCAAAACATTGGAG	80176
rs144529510	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9318241	ACCACGAATGCAGCC[A/G]GCAGCAGAACAGTGA	80176
rs144546742	in-del	-/AC	0.0926964	0.194308	intron-variant	SPSB1	GRCh38.p7	1:9305518	TCGGATGAAGGAGTA[-/AC]GGTAAGACCGGTGGC	80176
rs144658543	snp	A/G	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9321560	AGAGGGTGTTTGAGA[A/G]ACTGATGAGTCAGTG	80176
rs144706924	snp	C/T	0.0174175	0.0916809	intron-variant	SPSB1	GRCh38.p7	1:9306672	CTTACTCTTCAGCAC[C/T]ATTTGCCACAAAAGA	80176
rs144739375	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9355376	TGACCAAGCAAATGC[C/G]CACTGTCATGGCTGA	80176
rs144795029	snp	C/T	0.0138799	0.0821421	intron-variant	SPSB1	GRCh38.p7	1:9340866	CGAGCACATGAAACG[C/T]ACATTTGTAGTCCTC	80176
rs144801831	in-del	-/CCT	0.180702	0.240204	intron-variant	SPSB1	GRCh38.p7	1:9301541	ATGTATGTGGATAGA[-/CCT]CCTGAGTGCGCACAG	80176
rs144820475	snp	C/G	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9310286	AGCTTCAAGCAAACT[C/G]AAGATTCACAGGATT	80176
rs144903502	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9296594	TGTGCACATGTGTAC[A/G]CACACATACATATGC	80176
rs144963825	snp	A/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9336854	TATAGTTCTTTCTAT[A/T]GTCCCTGTCCAGAGA	80176
rs145000244	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9317932	TCGCTCCGCGAGTTT[C/G]TTAAGGGCCCCTGTG	80176
rs145067463	snp	A/G	0.0509478	0.151255	intron-variant	SPSB1	GRCh38.p7	1:9341882	TAATTTTGTATTTTT[A/G]GTAGAGATGGGGTTT	80176
rs145096443	snp	A/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9322801	GGTCTGATGGTCAGC[A/G]GGGGCAGGCAGCCCT	80176
rs145135271	snp	G/T	0.00318978	0.0398085	intron-variant	SPSB1	GRCh38.p7	1:9326115	CTGGGCTGCCGACAC[G/T]TGGGGAGGTCGGGTG	80176
rs145137377	snp	A/G	0.00795532	0.062565	intron-variant	SPSB1	GRCh38.p7	1:9358226	TTTGGAAGCCTCCCC[A/G]CCCCTCTTTCTCTTG	80176
rs145170211	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9362036	TTGGTGTGGTTTGTC[A/G]TGGTTGAAGGTTCAG	80176
rs145274486	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9296593	ATGTGCACATGTGTA[C/T]ACACACATACATATG	80176
rs145287530	in-del	-/A	0.379158	0.214052	intron-variant	SPSB1	GRCh38.p7	1:9343363	ATCGTACAATGTGTG[-/A]CCTTTTATATCTGGC	80176
rs145347459	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9294469	AGCCGGGCATGCTGG[A/G]CCACAGACACCCCAC	80176
rs145389577	snp	C/T	0.00755907	0.0610114	intron-variant	SPSB1	GRCh38.p7	1:9344503	CATTCCCTGGCTGAG[C/T]GCTCTCCTGCACTTG	80176
rs145426139	snp	A/G	0.0103295	0.0711199	intron-variant	SPSB1	GRCh38.p7	1:9331122	TGAATGCTTGTGGAA[A/G]TGTCTCCAGGCTCAC	80176
rs145435274	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9343350	TCGTCGAAAGGGAAT[A/C]GTACAATGTGTGACC	80176
rs145499213	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9343146	GCATTGAGTACATTC[A/G]CAATATAGTATACTA	80176
rs145515873	snp	C/T	0.0275645	0.114116	intron-variant	SPSB1	GRCh38.p7	1:9307074	CTGGGATTACAGGCA[C/T]GTGCCACCACGCCTG	80176
rs145563178	snp	C/G	0.00279162	0.0372561	intron-variant	SPSB1	GRCh38.p7	1:9353940	AAAAAAAGGAACCCT[C/G]TGTCTCACATCAGAA	80176
rs145587082	snp	C/G/T	0.00517822	0.0506191	intron-variant	SPSB1	GRCh38.p7	1:9338816	AGCTTCCTGGGGGCG[C/G/T]TCCCGCCTTGCTCTG	80176
rs145661332	snp	C/T	0.00716266	0.059414	intron-variant	SPSB1	GRCh38.p7	1:9303768	TATGGTTTAAGGAGA[C/T]GCCAGTGGGTGCCTC	80176
rs145661459	in-del	-/CCCT			intron-variant	SPSB1	GRCh38.p7	1:9362180	ACCAGGGCCACCCAC[-/CCCT]CCTCCCTCCCTCCCT	80176
rs145706825	snp	C/T	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9321584	GTCAGTGAGGGAGAC[C/T]GATGCATAGGCAGCT	80176
rs145753296	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9368313	GATATGTATGCCTCG[C/T]CCGCCCTCCCTGGGC	80176
rs145774819	snp	A/G	0.0189856	0.0955633	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9290981	TTGAGATGGAGTCTC[A/G]CTCTGTTGCCCAGGC	80176
rs145776925	snp	C/T	0.00716266	0.059414			GRCh38.p7	1:9357796	GCCCAGCTGGGAGTC[C/T]GTGGTAGCAGGAGGG	80176
rs145778199	snp	A/G	0.00199481	0.0315187			GRCh38.p7	1:9360777	TAATGAAGTACATCC[A/G]CAAGGCCCTGTTTCC	80176
rs145804748	in-del	-/TG	0.0182019	0.0936463	intron-variant	SPSB1	GRCh38.p7	1:9315654	CCTCCACCTGTGGGA[-/TG]CAGCCTGGTTTCGAC	80176
rs145845357	snp	A/G	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9309813	CACCATTGCACTCCA[A/G]CCTGGGCAATAGTGT	80176
rs145887952	snp	A/C	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9365150	GCGTGAGCCACCACA[A/C]CTGGCCTGTTTTCAT	80176
rs145906145	snp	C/T	0.000813242	0.0201484	missense	SPSB1	GRCh38.p7	1:9355944	ACATGAGGGACCCCA[C/T]GTACAGGCCCCTGAA	80176
rs145936172	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9356660	GGGCTCAGGCCAAAA[A/G]TTGATTCATTGGAAC	80176
rs145936483	snp	C/T	0.0240643	0.107019	intron-variant	SPSB1	GRCh38.p7	1:9313760	CCAGTCCAGCCTGCC[C/T]GCTGTGCTTCAGTGG	80176
rs145977101	snp	A/G	0.00358779	0.0422022	intron-variant	SPSB1	GRCh38.p7	1:9353155	GTACTCTGCACCCCC[A/G]CTCCATGCAGCTCTG	80176
rs146016535	snp	A/G	0.0356815	0.128715	intron-variant	SPSB1	GRCh38.p7	1:9301934	TCTGGATACAGATTC[A/G]TCTTCCCTGCACACA	80176
rs146035293	snp	A/C	0.00597247	0.0543191	intron-variant	SPSB1	GRCh38.p7	1:9305320	CTTCAGCAGGTAGCC[A/C]TGCCATCCACGGTCC	80176
rs146056457	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9330067	CCTCCATTCTGAGGA[C/T]ACAAGGCATCTCTTC	80176
rs146099521	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9366965	CTAGTGCTGGGGGTG[C/T]GTGCCAGGAAGAGCT	80176
rs146179713	in-del	-/AAT/AATAAT			intron-variant	SPSB1	GRCh38.p7	1:9330476	TCTCAAAATAATAAC[-/AAT/AATAAT]AATAATAATAATAAT	80176
rs146261197	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9333545	CATGTTGGGCAGGCT[A/G]GTCTCGAACTCTTGA	80176
rs146299335	snp	C/T	0.0123036	0.0774623	intron-variant	SPSB1	GRCh38.p7	1:9339606	CAGGGCTGGTGTGGC[C/T]ACTGGTGTCTAAGGG	80176
rs146313067	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9357136	ATGGATGGATGAGTG[A/G]ATGGATGGATGGGTG	80176
rs146341095	snp	C/T	0.0111196	0.0737302	intron-variant	SPSB1	GRCh38.p7	1:9333926	TGGCCAGGGATGCTC[C/T]GCCACATTCCTTCTC	80176
rs146382820	snp	A/G	0.0134861	0.0810011	intron-variant	SPSB1	GRCh38.p7	1:9352580	AAAAGCTGATCTCCG[A/G]TCTCGCTGAGACAGG	80176
rs146443380	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9349397	GGGCCAGAGCTGTGC[C/T]GGGCCAGGAGTGGGG	80176
rs146462573	snp	A/G	0.0402882	0.136092	intron-variant	SPSB1	GRCh38.p7	1:9310164	TGCCGTGGGAAGGCC[A/G]CAGAGTCTAGGGGCC	80176
rs146487525	snp	G/T	0.00953873	0.0683987	intron-variant	SPSB1	GRCh38.p7	1:9346574	TCTGAAAGCATTTTG[G/T]GGGAAGGTGGGGTCT	80176
rs146567168	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9364543	AACCCTGTGAGGAGC[C/T]GGGTGGGTGGAACCC	80176
rs146581986	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9315981	AGTTCTGCAGCCAGC[A/G]GGGCCTCTTGGCAGA	80176
rs146584823	snp	A/G	0.00636936	0.0560724	intron-variant	SPSB1	GRCh38.p7	1:9325761	ACGGGGGCAAAGGAC[A/G]TTTGCCATTTGGGCA	80176
rs146610581	in-del	-/GT			intron-variant	SPSB1	GRCh38.p7	1:9295192	TACCCAGTAGATGGA[-/GT]GTGTGTGTGTGTGTG	80176
rs146682292	snp	A/T	0.00279162	0.0372561	intron-variant	SPSB1	GRCh38.p7	1:9314606	ACAAAGAATTGCAGA[A/T]AGTGGCAGCCTCATC	80176
rs146699057	snp	A/G	3.34342e-05	0.00408852	missense	SPSB1	GRCh38.p7	1:9367505	GCCTGGCCCTGGGGA[A/G]GGAGCGCCTGGGGGA	80176
rs146724700	snp	A/G	0.00438332	0.0466095	intron-variant	SPSB1	GRCh38.p7	1:9310415	AAGACCTAAAGGGCC[A/G]GGCACAGTAGCTCAT	80176
rs146779365	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9309301	GAGAGAGAGAGAGAG[A/T]GTGTGTGTGTGTGTG	80176
rs146825591	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9294226	TGTGTGTGTCTTTGC[A/G]TGTGTGTGTCTTTGT	80176
rs146849149	snp	A/G	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9326481	AACAGGGAGGCAGGA[A/G]GTTCACCTCGAGACC	80176
rs146864205	in-del	-/GTGA	0.495818	0.0455352	intron-variant	SPSB1	GRCh38.p7	1:9294103	TGTCTGTGTGTCTTT[-/GTGA]TGTGTGTGTCTGTGT	80176
rs146925082	snp	C/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9296748	GACTGTTACTCTATG[C/T]GGGGCAAGAGTCGGG	80176
rs146941049	snp	C/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9300369	CAGAAGACTGCAACA[C/G]GTCCAGGTTGCTGTG	80176
rs146958897	in-del	-/C			intron-variant	SPSB1	GRCh38.p7	1:9362516	AAGCTGCTTGCAGGG[-/C]CCAGCCACAGGAGCC	80176
rs146961224	snp	A/G/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9331746	TGGTACTTGCTCTCC[A/G/T]CTTCCTGTGTGTAGA	80176
rs147032369	snp	A/C	0.00478085	0.0486577	intron-variant	SPSB1	GRCh38.p7	1:9355079	CGGGGGATGAGCCCC[A/C]CTTGCTGTCTGAATC	80176
rs147032816	snp	A/C	0.00557542	0.0525036	intron-variant	SPSB1	GRCh38.p7	1:9311115	AAAGCCAAGTCCTTA[A/C]CCCCACGCCACTCTC	80176
rs147049251	snp	A/G	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9315348	CCACAGGAAGGCATC[A/G]CAGCAGCAGTCAGGA	80176
rs147067601	in-del	-/G			intron-variant	SPSB1	GRCh38.p7	1:9354430	ACCCCAAACCAGGCT[-/G]GCCCTCCTTGGCCTC	80176
rs147068414	snp	A/G	0.00993419	0.0697739	intron-variant	SPSB1	GRCh38.p7	1:9350203	TGTGATGAGATTACA[A/G]CCTGGTCTTCAGGAA	80176
rs147156486	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9363200	GACCGGGCCCTATGC[A/G]CCATCAGTTTCCTCC	80176
rs147188209	snp	C/G	0.00676609	0.0577691	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291651	TCTTGAACTCCTGGG[C/G]TTAAGTGATCTGCCT	80176
rs147192050	snp	C/T	0.00279162	0.0372561	intron-variant	SPSB1	GRCh38.p7	1:9359429	CGTTCTGCGGCTGGG[C/T]GCGGTGGCTCATGCC	80176
rs147199930	in-del	-/GATA	0.0592355	0.161582	intron-variant	SPSB1	GRCh38.p7	1:9356943	ATGTTTGGATTGATA[-/GATA]AGTGGTTGAACAAAC	80176
rs147204191	snp	G/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9297682	GTTTGGTTGGCTGAC[G/T]GGAACATGGATCAAA	80176
rs147260134	snp	A/G	0.0263992	0.111815	intron-variant	SPSB1	GRCh38.p7	1:9312295	GCCTCCCAAAGCTCT[A/G]GGATTACAGGCACGA	80176
rs147296846	in-del	-/G			intron-variant	SPSB1	GRCh38.p7	1:9338854	TCCTGAATGGGATGA[-/G]GGGGGTCTTTGGGTC	80176
rs147365887	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9328735	AAGATGGTTTTGTCC[A/C]AGGAATACCCTGCGT	80176
rs147382491	snp	A/G	0.0341408	0.126114	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291344	GATGCCCGCCACCAC[A/G]CCTGGCTAATTTTTT	80176
rs147402643	snp	C/G	0.00874735	0.0655527	intron-variant	SPSB1	GRCh38.p7	1:9324601	CCCTGGGAGAAAACC[C/G]AAACCTGGGTTTCCC	80176
rs147556719	in-del	-/ACT			intron-variant	SPSB1	GRCh38.p7	1:9325221	CCAATGCCTCCCACC[-/ACT]ACCACCCCCCCCCCC	80176
rs147668996	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9357196	ATGAGTGGATGGATG[A/G]ATGGGTGGATGGATC	80176
rs147704254	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9355149	CTCCTGGTGCCTTTC[A/G]TGCCAAGCGCACACA	80176
rs147734161	snp	C/T	0.00517822	0.0506191	intron-variant	SPSB1	GRCh38.p7	1:9303945	GGGAAGCCCAGTGGT[C/T]TGGCATTTGTGTAGA	80176
rs147807989	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9368601	TTTGATTTTGCTTTT[A/G]CTTTTCTAGCTGAGA	80176
rs147841390	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9318392	TTCCAGGCTGCCTTG[C/T]GGACAGACAGGGAAT	80176
rs147858113	snp	A/G	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9321204	TTAGTCTGCAGAGGC[A/G]TCTCAGGCGGTGGGC	80176
rs147921232	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9296592	GATGTGCACATGTGT[A/G]CACACACATACATAT	80176
rs147964349	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9341322	AGTGGGGGAGAGTTC[A/G]GAGATGCAGGTAGAA	80176
rs148035931	snp	C/T	0.00755907	0.0610114	downstream-variant-500B	SPSB1	GRCh38.p7	1:9369612	GTCCAGCCAGCTCCA[C/T]GGCCCACAGTTTTCA	80176
rs148038986	in-del	-/A	0.135484	0.22223	intron-variant	SPSB1	GRCh38.p7	1:9335157	AATGCACCATTTTGT[-/A]AAATGGTGCATTTTC	80176
rs148088980	snp	C/T	0.00953873	0.0683987	intron-variant	SPSB1	GRCh38.p7	1:9343824	AGAGTCTCGCTCTGT[C/T]GCCTAGGCTGGAGTG	80176
rs148132290	in-del	-/GGTGA	0.354235	0.227234	intron-variant	SPSB1	GRCh38.p7	1:9365566	AGTGGCCTCTTGCGT[-/GGTGA]GATGTAGGAAACAAT	80176
rs148213453	snp	A/G	0.00358779	0.0422022	intron-variant	SPSB1	GRCh38.p7	1:9301300	GTTCGAGACCAGCCT[A/G]AGCAACATAGTGAGA	80176
rs148299288	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9309054	AGGCTGGGGGGTTTC[A/G]TGGTAGGGGACCAGG	80176
rs148338920	in-del	-/TT	0.482979	0.0906686	intron-variant	SPSB1	GRCh38.p7	1:9306923	CTTTTACTTTTCTTC[-/TT]TTCTTCTTTTTTTTT	80176
rs148353592	snp	C/T	0.00795532	0.062565	intron-variant	SPSB1	GRCh38.p7	1:9312440	GAGGTATTATGCACA[C/T]GCCACGCAGTTCGCC	80176
rs148367683	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9296096	TGGCAGCCAGGTGCC[C/T]GGCTCTGTGCTACAG	80176
rs148389657	snp	A/G	0.00398564	0.0444627	intron-variant	SPSB1	GRCh38.p7	1:9351317	TGGCCCAAAGGCAGC[A/G]TCCCTCTGTAGGGCC	80176
rs148407034	snp	A/C	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9309934	TTCAACTTCCTGGTC[A/C]TTTTGTTTGGCTGTG	80176
rs148425447	snp	G/T	0.00358779	0.0422022	intron-variant	SPSB1	GRCh38.p7	1:9359286	ACATTGGAGGGTGGG[G/T]CACTGTCACAACTCC	80176
rs148442962	snp	A/G	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9354291	AACAAGCGACCCAGC[A/G]TGACTCTCTCCCGGC	80176
rs148476532	snp	C/G	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9299484	TCTCTCTCTCTCTCT[C/G]TCTCTTTTTTTGAGA	80176
rs148477262	snp	A/G	0.0189856	0.0955633	intron-variant	SPSB1	GRCh38.p7	1:9363764	TAGTGCAGTGGCGCA[A/G]TCTCAGCTCACTGCA	80176
rs148617984	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9344527	GCACTTGGCATTCAC[A/G]ATTCCAAGCTATCAG	80176
rs148650389	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9356838	ATGAATGAATAGATG[A/G]ATGAATGATTGGTTG	80176
rs148684133	snp	C/T	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9329649	AGTGAGCCGAGATCA[C/T]ACCACTGCACTCCAG	80176
rs148714521	in-del	-/A	0.00279162	0.0372561	intron-variant	SPSB1	GRCh38.p7	1:9295146	CACTCCTGCTCTCTT[-/A]ACAGCTGCTTTTCTT	80176
rs148728532	in-del	-/TGTG	0.454555	0.143726	intron-variant	SPSB1	GRCh38.p7	1:9294029	GAGACTCTAAGTGAC[-/TGTG]TGTGTGTGTGTGTGT	80176
rs148737932	snp	C/T	0.00318978	0.0398085	intron-variant	SPSB1	GRCh38.p7	1:9302717	CTTTTGAAGTTGCAA[C/T]TACAATGCCAGCTAG	80176
rs148753648	in-del	-/GA	0.00279162	0.0372561	intron-variant	SPSB1	GRCh38.p7	1:9332518	AGGGTCACTGCTGGG[-/GA]GAGATGATATTTGGT	80176
rs148774372	snp	C/G	0.0166446	0.0897958	intron-variant	SPSB1	GRCh38.p7	1:9340285	AGAGGAGGGGCCTGG[C/G]GGGGAAGGCAGGGAC	80176
rs148848684	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9304651	GTTCCCAGCTAGTTT[A/G]GGGGTCATCGTGAAT	80176
rs148880443	snp	C/T	0.00318978	0.0398085	intron-variant	SPSB1	GRCh38.p7	1:9314663	GCATAGGTCTTCTTA[C/T]ATCGTCTTGTTTTTC	80176
rs148951951	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9360917	CTCCCTGTGCTGCCA[C/T]CTGTGGGGGGTGAAA	80176
rs149018843	snp	C/G/T	8.62424e-05	0.00656618	synonymous-codon	SPSB1	GRCh38.p7	1:9367449	CTCTGTCTCCCCAGC[C/G/T]GAGCCGCTGCCGCTC	80176
rs149056214	snp	C/T	0.0182019	0.0936463	intron-variant	SPSB1	GRCh38.p7	1:9337566	CACCCCAGCCCTCTG[C/T]GGGCTTTTCTCCCCT	80176
rs149074099	snp	C/T	0.00914312	0.0669923	intron-variant	SPSB1	GRCh38.p7	1:9318075	GGCAGGTTGGGGAAA[C/T]GCAGCGATTGTTCTG	80176
rs149128271	snp	C/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9357253	TGGATAAATGAACAG[C/G]TGGATGAGTGGGTAG	80176
rs149145688	snp	C/T	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9347643	TCGTGTTACATTTTC[C/T]GTTACGTCACCACTT	80176
rs149216123	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9331201	TGGTGCAAACATATC[A/G]GAGTGGTCTGCCTAA	80176
rs149230974	in-del	-/C	0.00835141	0.0640778	intron-variant	SPSB1	GRCh38.p7	1:9353332	CTCTCCCCCTTCCCT[-/C]CCGCAGCTTGAGGCG	80176
rs149234269	snp	C/T	0.0115144	0.0749975	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291343	AGATGCCCGCCACCA[C/T]GCCTGGCTAATTTTT	80176
rs149289364	snp	C/T	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9298705	AGTCAGAGAAGGGGC[C/T]TATGGAGGTCAGGTG	80176
rs149321176	snp	A/G	0.00438332	0.0466095	intron-variant	SPSB1	GRCh38.p7	1:9308758	AGAGAGGTTTTCTGC[A/G]TTGCAGGAAGTGGCA	80176
rs149322691	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9333417	CTCACTGCAACCTCC[A/G]CCTCCCAGGTTCAGG	80176
rs149355700	snp	A/G	0.00636936	0.0560724	intron-variant	SPSB1	GRCh38.p7	1:9310933	ATAAATTATACGTAC[A/G]TGTCAGGGTTCTTCT	80176
rs149395215	snp	A/G	1.80387e-05	0.00300317	utr-variant-5-prime	SPSB1	GRCh38.p7	1:9355876	AGTCGGTAAGAAGGT[A/G]AAGCCAGGGGCGAAC	80176
rs149411878	snp	C/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9316557	GCTGGATGGCGAGGA[C/G]GGGGGGGCTGATCGA	80176
rs149449237	snp	A/G	0.0170251	0.090679	intron-variant	SPSB1	GRCh38.p7	1:9323268	AACATTCTAGTTCCC[A/G]CCGAGCCGAGGGGGG	80176
rs149501005	snp	A/G	0.00636936	0.0560724	intron-variant	SPSB1	GRCh38.p7	1:9329280	GAAAGGTGAGATCCC[A/G]GATGGGTGGATGGGT	80176
rs149589725	snp	C/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9340211	CTCTCCTTGGGCAGG[C/T]TTTCTCTCCTGTCTG	80176
rs149634344	in-del	-/GATG	0.309154	0.242901	intron-variant	SPSB1	GRCh38.p7	1:9357268	GTGGATGAGTGGGTA[-/GATG]GATGGATGGATGGAT	80176
rs149657401	in-del	-/CT			intron-variant	SPSB1	GRCh38.p7	1:9337227	AGTCAGGATCTGAGC[-/CT]CTAACCCCCGGGATT	80176
rs149677145	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9349016	TGGTGGGGTATTCCT[C/T]CCACTGGGAGAAGAA	80176
rs149729030	snp	C/T	0.0252325	0.109451	intron-variant	SPSB1	GRCh38.p7	1:9353849	CTTGAACCCAGGAAG[C/T]GGAGGTTGCAGTGAG	80176
rs149738454	in-del	-/GGGTGG	0.384785	0.210554	intron-variant	SPSB1	GRCh38.p7	1:9360208	GCTTAGAGGCCAGGA[-/GGGTGG]GGGCTGAAGGGACCC	80176
rs149765650	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9360622	GGCGTCCCTTGGTCT[A/G]TAGATGCCTCCCTGA	80176
rs149818899	snp	C/T	0.0107246	0.0724382	intron-variant	SPSB1	GRCh38.p7	1:9365006	ACAGGCCCATGCCAC[C/T]ATGCCTGGCTCATTT	80176
rs149887207	snp	A/G	0.0178098	0.0926698	intron-variant	SPSB1	GRCh38.p7	1:9313542	TGGGAACAGGCACCT[A/G]ATCTGGGGTGGGAGG	80176
rs149933700	snp	C/T	4.948e-05	0.00497369	synonymous-codon	SPSB1	GRCh38.p7	1:9356012	CGGCTGGATCTGCTA[C/T]TGGACATGCCCCCTG	80176
rs149942378	snp	A/G	0.00716266	0.059414	intron-variant	SPSB1	GRCh38.p7	1:9317350	GCTTTGATGATACCC[A/G]GTATATAGTAAGTGC	80176
rs150030288	snp	A/G	0.00557542	0.0525036	intron-variant	SPSB1	GRCh38.p7	1:9330801	GTTGAGTACATTACC[A/G]GATCGTACGATCATT	80176
rs150047544	in-del	-/TG			intron-variant	SPSB1	GRCh38.p7	1:9294029	GAGACTCTAAGTGAC[-/TG]TGTGTGTGTGTGTGT	80176
rs150066443	snp	A/C	0.00347045	0.0415112	intron-variant	SPSB1	GRCh38.p7	1:9367412	GCTGAACACCCACCC[A/C]AGCTGCGCTGACCTG	80176
rs150082897	snp	A/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9304135	TGTCCCGGAGCTGGG[A/G]CATCCTCCTTCTCCT	80176
rs150084069	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9328410	GAGCCTTTAAGATGC[C/T]GATGCGTTTGTGACT	80176
rs150100498	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291247	CTGGAGTGCAGTGGC[A/G]CAATCTCGGCTCACT	80176
rs150112077	in-del	-/ACAGTC	0.079617	0.182947	intron-variant	SPSB1	GRCh38.p7	1:9325567	GGCACCGTGGAACAG[-/ACAGTC]ACTCAGCAGGCATGT	80176
rs150170807	snp	C/G	0.0178098	0.0926698	intron-variant	SPSB1	GRCh38.p7	1:9346749	GGGGTGGAACAGCCA[C/G]CGGTGTTTCTGATGG	80176
rs150207660	snp	C/T	0.0107246	0.0724382	intron-variant	SPSB1	GRCh38.p7	1:9355576	CAGCTAGCCAGGGAA[C/T]GGGGGATTTCATTCT	80176
rs150294962	snp	A/G	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9362479	GACATTCTAGAATCC[A/G]TGTCCTGGAGCGTGG	80176
rs150326449	snp	A/G	0.00358779	0.0422022	intron-variant	SPSB1	GRCh38.p7	1:9307857	TAAATCCATGATGTG[A/G]TCTTCGGGGTGCGCG	80176
rs150359563	in-del	-/TGTC			intron-variant	SPSB1	GRCh38.p7	1:9294171	GTTTGTGTCTCTGAG[-/TGTC]CTGTCTCTGCAAATG	80176
rs150378358	snp	A/G	0.00279162	0.0372561	intron-variant	SPSB1	GRCh38.p7	1:9310764	GCAGATGGGGGTTGG[A/G]GGAGATTCTCAAGTG	80176
rs150468284	snp	A/G	0.0142736	0.0832652	intron-variant	SPSB1	GRCh38.p7	1:9319547	CTCCCCGCTGAAGTC[A/G]AGTGGAGGAGGTGGG	80176
rs150470875	snp	C/T	0.0150606	0.0854603	intron-variant	SPSB1	GRCh38.p7	1:9323143	TGCCGGACATTCCTT[C/T]CTGCTGCCATGTTGG	80176
rs150526150	snp	A/C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9320794	GTTTCTTGTTTCCTC[A/C/G]TGGGGGATTTTAAAT	80176
rs150587187	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9294174	TGTGTCTCTGAGTGT[C/G]TGTCTCTGCAAATGT	80176
rs150599247	in-del	-/AGTTCAAGACCAG			intron-variant	SPSB1	GRCh38.p7	1:9318970	GAGGCGGGCACATCA[-/AGTTCAAGACCAG]CCTGAGGTCATGCCT	80176
rs150610550	snp	A/G	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9306381	TCCAGCCTGGAGGAG[A/G]TGGAAGATGGATGGA	80176
rs150750508	snp	C/T	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9317027	CCAAGTGGAAACACA[C/T]GGTGGAATTTAGAAT	80176
rs150767893	snp	C/T	0.00755907	0.0610114	intron-variant	SPSB1	GRCh38.p7	1:9301580	TAGACCTCCCGAGTG[C/T]GCACAGGACATGAGG	80176
rs150768581	snp	C/G	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9366462	GCCATGTCTTCCTTT[C/G]CAGCATGGTTAGTGG	80176
rs150789519	snp	C/T	0.00358779	0.0422022	intron-variant	SPSB1	GRCh38.p7	1:9360041	TTTGAGACGCTTCTT[C/T]GACACATCCAGGGGG	80176
rs150823232	snp	C/T	0.00755907	0.0610114	intron-variant	SPSB1	GRCh38.p7	1:9364010	CAGCCTAGAAACATT[C/T]CTTCATGGGTTGATT	80176
rs150910785	snp	A/G	0.00358779	0.0422022	intron-variant	SPSB1	GRCh38.p7	1:9312510	TGTGGTCAGGCAGCC[A/G]TGGACACCGTCCTAG	80176
rs150978987	in-del	-/T	0.0596104	0.162024	intron-variant	SPSB1	GRCh38.p7	1:9297641	CTGCACTTGATGTTG[-/T]AGCTCAGGGGGTTAA	80176
rs150999345	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9325351	TCTTGCCACCTTTGG[A/G]GAGTGAGTTCTCAAT	80176
rs151019738	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9314972	TCCTTGGCACTGTAG[C/T]ATTCCTTTTGAAGTC	80176
rs151053267	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9322468	CCTGCTCACCTGCAC[C/G]ATCTGTCACCTACTG	80176
rs151089438	snp	C/T	0.0452528	0.143452	intron-variant	SPSB1	GRCh38.p7	1:9334448	CTGGTCTCGAACTTC[C/T]GGCCTCAAGTGATCC	80176
rs151142942	snp	A/G	0.00318978	0.0398085	intron-variant	SPSB1	GRCh38.p7	1:9307760	TTTGTATCTTTTCCC[A/G]TTGATCTATTAAAAA	80176
rs151179247	snp	C/T	0.00953873	0.0683987	intron-variant	SPSB1	GRCh38.p7	1:9345517	GGTTGCTGTGTGTCC[C/T]TGGGGTCCCTCAAGA	80176
rs151208904	snp	C/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9293915	GAGTGTGTCTGTGTG[C/T]TCATGTGGGTGTGTG	80176
rs151230958	snp	C/T	0.00358779	0.0422022	intron-variant	SPSB1	GRCh38.p7	1:9349518	CCAGCGCCGTAGATG[C/T]GTGTCAGATTTGACA	80176
rs151267368	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9357405	TGGTCTTTGTTTCTC[C/T]GGGTGACCTGCCTCC	80176
rs151297378	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9303693	TGTGTCTTTGCTATG[C/T]AGGATAGTAGTGTCA	80176
rs151301224	snp	A/G	0.00358779	0.0422022	intron-variant	SPSB1	GRCh38.p7	1:9367071	AGCAGGGATCGCCTG[A/G]GTTCGAATCCTAGCT	80176
rs180757095	snp	A/G	0.00398564	0.0444627	intron-variant	SPSB1	GRCh38.p7	1:9349574	GGAGCGTGGGTGGGT[A/G]GACGGCTTGCCTGCC	80176
rs180794672	snp	A/G	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9313489	GACGCAGACCCAGGC[A/G]GTCTGTGCTCCGAAC	80176
rs180810621	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9300527	GGAGCAAGGCCCTGC[C/T]ATCATCCACAAATAA	80176
rs180812908	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9332716	TCACAAAACTAGGAG[C/T]GTTTCAGGTCAAGGG	80176
rs180850085	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9364516	GCTGGGTGTTTTACC[C/G]GAGGGAAACCCAACC	80176
rs180877198	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9345723	GTGTTTACAGCAGGT[A/G]CATTTTGGGTCTTTT	80176
rs180878859	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9310588	TGATCCCAGCTACTC[A/T]GGAGGCTGAGGCAGG	80176
rs180885990	snp	C/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9328441	CTCTAGGAGGGGATA[C/T]GATGTTTCCTAACCC	80176
rs180930304	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9336521	GTGAGCCACCACGTC[C/T]GGCTCCTCCTCCTGG	80176
rs180930494	snp	C/G	0.00279162	0.0372561	intron-variant	SPSB1	GRCh38.p7	1:9303332	AAAGAACCACAGCCA[C/G]CTGAGGTGCTTGTTG	80176
rs180957563	snp	G/T	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9317352	TTTGATGATACCCGG[G/T]ATATAGTAAGTGCTT	80176
rs180965569	snp	C/T	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9297389	GTGACAAGGGCTTGA[C/T]GGGTGCCCCAGTTGT	80176
rs181100488	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9299679	AGACAGGGTTTCACT[A/G]TGTTGGTCAGGCTGG	80176
rs181317570	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9368521	GTAACCAGCTAACTC[C/T]TGGGCTCAGGCACCC	80176
rs181320871	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9323869	TGGGACCTTGGAACC[C/T]GAGCCTTCTCCCATC	80176
rs181343894	snp	A/G	0.0142736	0.0832652	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9292349	ATGCCAGGTGCCCGC[A/G]CCCTCAGGGTCTCGA	80176
rs181351110	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9307958	TGCCCCATGGGGACC[A/G]ACCCTGAGGCTGGGA	80176
rs181354584	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9348798	CCAGGCTGCCACCGA[A/G]AAATCCAGTAGGGTC	80176
rs181360646	snp	C/T	0.00279162	0.0372561	intron-variant	SPSB1	GRCh38.p7	1:9331788	ATCTCTGTATTGACT[C/T]TGTAGCAATCTGGAG	80176
rs181435155	snp	A/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9359975	TGAGCAGGTGAAGGC[A/G]GGGGCTGCTGACCCG	80176
rs181454948	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9328083	GCTTAGCTGGAGCAG[A/G]TGATGAACAGCCCCT	80176
rs181479899	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9296771	GAGTCGGGAGATGTA[C/T]GTCCTTTCTGACTTG	80176
rs181484975	snp	A/G	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9310357	TGAGGTTCTTGGGGC[A/G]CCTTCCTGGATTTCT	80176
rs181517189	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9354968	GGACTTTCCTCCCCA[C/G]ATGTGCTGTTGAGAC	80176
rs181581836	snp	A/C	0.00636936	0.0560724	intron-variant	SPSB1	GRCh38.p7	1:9342343	TGACAAGTCCAGAAA[A/C]TGTGTGCATCAGCCT	80176
rs181598364	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9312998	GAGTGCTTGCTCTGT[A/G]CCTGGCACTGTTCTG	80176
rs181603472	snp	C/G	0.00318978	0.0398085	intron-variant	SPSB1	GRCh38.p7	1:9350454	GGATGAAAACTTTCA[C/G]TAAGGGAATGGAGAG	80176
rs181607713	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9333458	GCCTCAGCTTCCCAA[C/G]TAGGTGGGACTACAG	80176
rs181621827	snp	C/T	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9314392	GCAGCTATCCTGGTA[C/T]CTTCCTGATGGGAAG	80176
rs181634653	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9301151	TTGGCTGGATGGTCA[A/G]GGATTTGGGGACTTG	80176
rs181646165	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9319738	AAAGGTCCGCTGTAG[C/T]GAAGGGAGGGTACTA	80176
rs181655247	snp	C/T	0.00517822	0.0506191	intron-variant	SPSB1	GRCh38.p7	1:9345002	GTTTGGTCGGATCCC[C/T]TATGTCCAAGAGACT	80176
rs181675324	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9338066	GGGAGCAGGTTTGAA[C/T]TGGTTCCTGGAAGAC	80176
rs181695024	snp	A/G	0.00279162	0.0372561	intron-variant	SPSB1	GRCh38.p7	1:9363952	GTGATCACCCACCTC[A/G]GCCTCCCAAAGTGCT	80176
rs181708495	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9304685	GACCTACAGGCTGGG[A/G]GACTAGGTCCATGGA	80176
rs181745252	snp	C/T	0.00358779	0.0422022	intron-variant	SPSB1	GRCh38.p7	1:9342152	TCAGAGCACAGGCCT[C/T]AGATGGTGGAGTTCT	80176
rs181771851	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9307228	CCACTGTGCCTGGCC[A/G]TCTTTTCTCAGTTGA	80176
rs182010797	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9323186	ATGGGGCCTCTGTCC[C/T]GGCACTCAGCCTTTT	80176
rs182021485	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9358930	ACATGTCCTGTGAAT[A/G]GGCGATTTCCTGCTT	80176
rs182042973	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9354583	TTTGGGAGGCCAAGC[C/T]GGGTGGATCACCTGA	80176
rs182048520	snp	C/T	0.0205511	0.0992634	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291431	ACCTCGTGATCCGCC[C/T]GCCTCGACCTCCCAA	80176
rs182051873	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9337145	ACATGAGAGGGGAAG[A/G]GGTGCTTTCTGGTCG	80176
rs182087838	snp	A/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9361001	CATAGTGAGGTCAGA[A/G]CCCACCCAAGTCCCC	80176
rs182091082	snp	C/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9304410	CTCTCCCTCTCGATC[C/T]TATGGGTTTTGCATC	80176
rs182104251	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9324600	GCCCTGGGAGAAAAC[C/T]CAAACCTGGGTTTCC	80176
rs182112116	snp	G/T	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9308752	TTTTTTAGAGAGGTT[G/T]TCTGCGTTGCAGGAA	80176
rs182113903	snp	A/G	0.00279162	0.0372561	intron-variant	SPSB1	GRCh38.p7	1:9342735	ATCCCGGACTCCTCC[A/G]GAGAAACTCCATCTA	80176
rs182230378	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9305330	TAGCCCTGCCATCCA[C/T]GGTCCACCCTGTCAC	80176
rs182247571	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9364760	GTGACCGTCCATGGG[G/T]GATGAAGAGCAGTGG	80176
rs182308742	snp	C/T	0.00358779	0.0422022	intron-variant	SPSB1	GRCh38.p7	1:9329746	AAAGAAAGAAGTTAG[C/T]GCTGGAGTCCAGGAG	80176
rs182435322	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9315950	TTCACGCGTGCGGCT[C/T]CGGGCATCCTGGTGC	80176
rs182440767	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9351362	GGAAGACAGGAGAAC[A/G]GTGATCTTTGATCAG	80176
rs182525872	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9346637	GGGGGTTGCCGGCAG[A/G]TGCTGTGCAGTCTGG	80176
rs182576131	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9338467	TAAGGCCACCCAGGA[C/T]AGCACTTGCTGGGGA	80176
rs182582357	snp	C/T	0.00438332	0.0466095	intron-variant	SPSB1	GRCh38.p7	1:9311719	CCAGGATGTTTCTGC[C/T]GGGGGTTGCCGAGTG	80176
rs182659875	snp	A/G	0.0103295	0.0711199	intron-variant	SPSB1	GRCh38.p7	1:9334441	GACCAGGCTGGTCTC[A/G]AACTTCTGGCCTCAA	80176
rs182663130	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9346970	CTGTAGAAATAATGT[C/G]CCTCTTCGGGATGGC	80176
rs182667936	snp	G/T	0.00318978	0.0398085	intron-variant	SPSB1	GRCh38.p7	1:9330626	GAGTATTTTGGGTTT[G/T]CCTGTCCTCTTCCTT	80176
rs182671215	snp	C/T	0.00398564	0.0444627	intron-variant	SPSB1	GRCh38.p7	1:9366288	AACTGGGCTGGCATT[C/T]CCAGTTTCCTGGGGC	80176
rs182772207	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9343988	AGAGATGGGGTTTCA[C/T]CGTGTTAGCCAGGAT	80176
rs182802326	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9326125	GACACGTGGGGAGGT[C/T]GGGTGGAATGTTCTT	80176
rs182806653	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9350710	CCACGCCCTTTGCGT[A/C]TGCTCCTCCTGGGTG	80176
rs182808144	snp	C/T	0.00279162	0.0372561	intron-variant	SPSB1	GRCh38.p7	1:9309380	TGGAGTGCAGTGGTG[C/T]GGTCACAGCTCACTG	80176
rs182869855	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9355328	ACTTCCCCTCTGAAC[C/T]GCAAGGCAAGGGCCA	80176
rs182877807	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9299289	GGTATATCAGCTCTC[C/T]AGCCCTATGTCACAG	80176
rs182901026	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9346834	GCTGGGTATGGGGAC[G/T]GACCAGCTGTTCTCT	80176
rs182925622	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9311345	CCCCTGATGGGTCTC[A/G]GCGTGGCTGAGGTTT	80176
rs182937235	snp	A/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9330403	CCGGGAGGCGGAGGT[A/T]GCAGTGAGCCAAGAT	80176
rs182940000	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9298910	GTGGAAACCATTAGC[A/G]TTGCCTCTGCCTGGG	80176
rs183125731	snp	A/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9362082	CTCCTCAAGATCAGA[A/G]CCTCCTCCCGGGTGC	80176
rs183134153	snp	C/T	0.0146672	0.084371	intron-variant	SPSB1	GRCh38.p7	1:9334223	CCTGAGTAGCTGGGA[C/T]TACAGGCGCCCACCA	80176
rs183157092	snp	A/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9301575	ACGGATAGACCTCCC[A/G]AGTGCGCACAGGACA	80176
rs183255471	snp	A/G	0.00517822	0.0506191	intron-variant	SPSB1	GRCh38.p7	1:9357075	GATGGATAAATGAAC[A/G]GATGGATGGGTGGGT	80176
rs183290646	snp	A/C	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9321156	AATCCCCCCAAAACA[A/C]AAAGCTGGAAAAAGC	80176
rs183412739	snp	C/T	0.0115144	0.0749975	intron-variant	SPSB1	GRCh38.p7	1:9320991	CCGAGTCCCTGGCTG[C/T]CACTCTCCAGGCCAA	80176
rs183412889	snp	C/T	0.00478085	0.0486577	intron-variant	SPSB1	GRCh38.p7	1:9339370	GGCTGTGACTCACCG[C/T]CAGGCCAGGTTCTGG	80176
rs183424636	snp	A/G	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9305636	ACTGCCAGGTGTTCC[A/G]TTCTCAGACCAGACT	80176
rs183426980	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9315428	TCTCACGCAAGTCTT[C/T]ACAATACAACACACA	80176
rs183441135	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9343634	CATTTTCATTTCTCC[A/G]GGCTCCTTTCTACCT	80176
rs183452987	snp	C/T	0.00438332	0.0466095	intron-variant	SPSB1	GRCh38.p7	1:9308990	TGGGCGGGCACCAGG[C/T]CTGCGTGGGTACAGA	80176
rs183539895	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9339536	ATTCCTGTCAGATGG[C/G]GTTGTTTGAAGTGAA	80176
rs183542464	snp	C/T	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9306467	GACAATAGCCATCAA[C/T]GATGTGGCATATCTG	80176
rs183542571	snp	C/T	0.00318978	0.0398085	intron-variant	SPSB1	GRCh38.p7	1:9364980	CCTTAGCCTCCCGAG[C/T]AGCCGGGACTACAGG	80176
rs183624842	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9317466	GATTTTCAGACCACC[A/G]GGTGAGAACAGACAG	80176
rs183629307	snp	C/T	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9344399	TCTGCCTTTCCTCAC[C/T]GCCAGACAGAGGGAG	80176
rs183637184	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9326332	CTGGAGGTGGAGACA[C/T]CCAGGGGCCACTCAG	80176
rs183647965	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9303729	GGTGGAACTATGACC[C/T]TGATACTGTCCTTGG	80176
rs183647992	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9362558	CAGCGAGGACATTGC[A/G]GAAGCCGGGGCATTC	80176
rs183701385	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9324718	CAGCATCTCCCGGAG[C/T]CCAGAATCTCTCTGG	80176
rs183711646	snp	C/G	0.242775	0.249896	intron-variant	SPSB1	GRCh38.p7	1:9293213	GCCGGGCGCGGGGGA[C/G]CGGGTGGAGTACGGG	80176
rs183916038	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9368933	CCAGCACCTGCCACC[A/G]CCTTTGCCATTTCTT	80176
rs183917894	snp	C/T	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9349198	GGTGACTCCAGGGCC[C/T]GTGGCTGCTCTCCGG	80176
rs184029834	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9361619	TACTGAGTTCTCGAC[A/G]TTTCCCTGTGCGGCC	80176
rs184035991	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9364339	ACAGCCAGGCCAGAC[C/G]ACAGGCTGCGATAAG	80176
rs184069566	snp	A/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9298588	TTTACCAGAGTGAAT[A/G]TGTATTGAGGAAAGG	80176
rs184076152	snp	G/T	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9345316	TTCTTGGAGATGGCC[G/T]TGGGGCTGCTTTTGG	80176
rs184117263	snp	C/T	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9354184	GCCAGCCCTCTGAGG[C/T]CCCTGGATTTCCGTG	80176
rs184152272	snp	C/T	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9321758	CACATGACTCTGAGT[C/T]GGTGGAGGAGGAGGA	80176
rs184158619	snp	A/G	0.0391387	0.134304	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291209	TTTTTTTTGTGAGAC[A/G]GAGTCTCGCTCTGTC	80176
rs184163050	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9306723	GATCCGAGAGATAGG[C/T]CAGCAGAGTGAATGT	80176
rs184172935	snp	A/G	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9296158	CTAAGCATAATAATA[A/G]CGGGAAATGGTTTCA	80176
rs184177728	snp	A/G	0.00438332	0.0466095	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9367741	CATGGGACAAGGACC[A/G]ATTCCAACACAGGCT	80176
rs184189595	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9331434	CTCCTGGGTTCAAGC[A/G]ATTCTCCTGCCTCTG	80176
rs184203284	snp	A/G	0.00438332	0.0466095	intron-variant	SPSB1	GRCh38.p7	1:9312824	CGCCCAGGGAAGGCT[A/G]CTTGGTTGGCATTTG	80176
rs184216217	snp	A/C	0.00993419	0.0697739	intron-variant	SPSB1	GRCh38.p7	1:9299639	CATGCGCCACCACAC[A/C]CAGCTAATTTTTTGT	80176
rs184219471	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9311029	CTAATTGTATCCTAT[C/T]GGGCCAATTTGGAGC	80176
rs184284373	snp	C/G	0.0785177	0.181917	intron-variant	SPSB1	GRCh38.p7	1:9336657	GCTGCCTGAGTTCAC[C/G]CGTGGCGCTGGGCTA	80176
rs184299870	snp	A/G	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9309516	TAGAGATGGGGTCTC[A/G]CCATGTTGCCTAGGC	80176
rs184344311	snp	C/T	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9302621	CGTACGAGTGGTCTC[C/T]GGAGTCTTTGACCTG	80176
rs184697672	snp	C/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9351485	TGTGTGACAGACAAA[C/G]GAGCAGAAGCTTGGA	80176
rs184702026	snp	A/G	0.00438332	0.0466095	intron-variant	SPSB1	GRCh38.p7	1:9316362	AGAGACAGCCCCTGG[A/G]GCACAAGGGAGGGGC	80176
rs184706105	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9334882	TCAAAATGTCCTTCC[A/G]TGTTAAGGCTGAGTA	80176
rs184707142	snp	C/G	0.00478085	0.0486577	intron-variant	SPSB1	GRCh38.p7	1:9340313	GACACTGGTGTTTGG[C/G]GACTGGCCGGAGCCC	80176
rs184722128	snp	A/G	0.00676609	0.0577691	intron-variant	SPSB1	GRCh38.p7	1:9313315	TGAGGCAGGAAAATC[A/G]CTTGGACCCGGGAGG	80176
rs184840982	snp	A/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9357472	TGCCAGCATATCATC[A/G]AGCTGGGGTTTGTAA	80176
rs184855798	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9331816	GAGGGTGCAACGTGC[A/G]ATCTCATTACTGCTT	80176
rs184869954	snp	C/T	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9299877	CTGAGGTGGGAGGAT[C/T]GCTTGAGCCTAGGAG	80176
rs184889144	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9303026	GAACGGGGGGTAAGG[C/T]TGCCACCTGGCTTCT	80176
rs184894364	snp	A/G	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9345926	GAGGGTGGTAACCAC[A/G]TGTCACAAGCCCTGC	80176
rs184894579	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9336373	CTGGGATTACAGGCA[C/T]GCACCACTATGCCCG	80176
rs184965827	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9352597	CTCGCTGAGACAGGC[A/G]TTCTGTGTGTTCAGT	80176
rs184991944	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9341725	TTGTTTTTTTGAGAC[A/G]GGGTTTCACTCTTGT	80176
rs185007700	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9317073	TGAGGGTTTGCTTCC[A/G]GTGCTCTCGCGAAGG	80176
rs185011108	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9358199	GCATGCGCAAACGCT[C/T]ACACATTTCTCTTTG	80176
rs185013916	snp	A/C/G	0.00557542	0.0525036	intron-variant	SPSB1	GRCh38.p7	1:9307075	TGGGATTACAGGCAC[A/C/G]TGCCACCACGCCTGG	80176
rs185021883	snp	C/T	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9322083	CGAGCACCCATCCTG[C/T]AAGGGGCTTGAATGG	80176
rs185246852	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9364542	CAACCCTGTGAGGAG[C/T]CGGGTGGGTGGAACC	80176
rs185262471	snp	A/G	0.00478085	0.0486577	intron-variant	SPSB1	GRCh38.p7	1:9320801	GTTTCCTCGTGGGGG[A/G]TTTTAAATTTATGTC	80176
rs185268163	snp	C/T	0.00597247	0.0543191	intron-variant	SPSB1	GRCh38.p7	1:9338738	GAGGGGGCGTCACCT[C/T]CCCCATATGACTTCG	80176
rs185397993	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9323927	GGCCCATGGGAAATT[C/G]AGGGGGTCTTTTCCT	80176
rs185415758	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9342345	ACAAGTCCAGAAACT[A/G]TGTGCATCAGCCTGG	80176
rs185422590	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9292373	GTCTCGAGGTCCGAG[A/G]CCCCCGTCCCCGTGG	80176
rs185433033	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9308599	TGATTCTGCCTGAAA[C/T]AGTCTTCACATGTAT	80176
rs185527795	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9344741	GGATGAGTGGATGCC[C/T]GGCCCCCTGACTGTC	80176
rs185538710	snp	C/T	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9310047	TGTTGCCCTAAAGCT[C/T]TCCTCAGGTGGGGGA	80176
rs185548954	snp	A/C	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9328226	AGGGCCTGGCCCATC[A/C]ATGGAATCTTGAAAC	80176
rs185575895	snp	A/G	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9297196	TCTTGAGTTTACTGC[A/G]TAGGCGATGGGTGGA	80176
rs185637796	snp	A/G	0.00358779	0.0422022	intron-variant	SPSB1	GRCh38.p7	1:9366368	ACCCGGGGTTTCTCT[A/G]TCTCCATGTGGCACA	80176
rs185644827	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9327787	TACTCGACTCTGTAG[C/T]GTGAAAGCAGCCACA	80176
rs185650914	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9363082	CTGGTACTGGTAGTG[A/G]CCAGCTGAAATGGGG	80176
rs185657833	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9330802	TTGAGTACATTACCG[G/T]ATCGTACGATCATTT	80176
rs185665241	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9296298	CTGAGGATTGCAGGT[A/G]ACTTGGCTAAGGTCT	80176
rs185678315	snp	A/G	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9299465	GCAACACAGTGAGAC[A/G]TCATCTCTCTCTCTC	80176
rs185777395	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9328794	GGGCTTCCCAACATG[A/G]CACTGTTGACATAGG	80176
rs185791032	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9297562	GAGTGGATATTAGGA[C/T]GTGGAACGAACATGA	80176
rs185802750	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291336	GACTTACAGATGCCC[A/G]CCACCACGCCTGGCT	80176
rs185823624	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9312099	CCTCCCTCCTCAGCC[C/T]CCTGAGTAGCTGGGA	80176
rs185902558	snp	C/T	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9315262	CAGCAGATTCCACTG[C/T]GACAAAAGACCCCGT	80176
rs185903370	snp	C/T	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9310612	AGGCAGGAGGATCAC[C/T]TGAGTTTGGGAGGTC	80176
rs185919917	snp	A/G	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9301446	TTGAGGCTGCAGTGA[A/G]CTGTGATTGCTCCAG	80176
rs186142050	snp	A/G	0.00478085	0.0486577	intron-variant	SPSB1	GRCh38.p7	1:9355384	CAAATGCCCACTGTC[A/G]TGGCTGAGTCCTGGT	80176
rs186274813	snp	A/T	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9333565	CGAACTCTTGACCTC[A/T]GGTGATCCGCCCACC	80176
rs186290644	snp	C/T	0.0111196	0.0737302	intron-variant	SPSB1	GRCh38.p7	1:9361080	GTGTCCTGGTGAGAT[C/T]GAATCCCAGGGTCTG	80176
rs186310262	snp	C/T	0.00636936	0.0560724	intron-variant	SPSB1	GRCh38.p7	1:9324639	GAAACTGCCAGTGGC[C/T]AGCCTGTCTTGTTCC	80176
rs186334761	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9343151	GAGTACATTCGCAAT[A/G]TAGTATACTACCACC	80176
rs186387573	snp	A/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9337483	GGTTTGGGGACAGGA[A/T]GCCCTCTTTGGGGGG	80176
rs186390814	snp	C/G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9298853	TCCACACACTGGTTC[C/G/T]CTGCCTTGTGCGGTG	80176
rs186396871	snp	A/G/T			intron-variant	SPSB1	GRCh38.p7	1:9354642	ACATGGTGAAACCCC[A/G/T]TCTCTACTAAAAATA	80176
rs186398069	snp	A/G	0.00636936	0.0560724	intron-variant	SPSB1	GRCh38.p7	1:9338141	GTCCCCTGTCCCCTC[A/G]CTCCTCCCCCCAGAC	80176
rs186404210	snp	C/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9318948	TAATCCCAGTACTTT[C/G]GGAGGCTGAGGCGGG	80176
rs186418693	snp	A/C	0.00318978	0.0398085	intron-variant	SPSB1	GRCh38.p7	1:9304594	TCGGTAACTAGTTGA[A/C]TGTGGGGTGTAGAGA	80176
rs186422716	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9360342	AGCTTTGGCAACAAG[A/G]AATTGGCAGTTGACC	80176
rs186453702	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9304832	TGCACACCACCACCC[C/T]CAGCTAATTTTTAAA	80176
rs186466098	snp	A/T	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9305395	GCTGCTGTTGTGGGC[A/T]GCCCAGTGACCTGTG	80176
rs186510102	snp	A/G	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9300740	GGAAGTGGTATATAT[A/G]GGATCAGGTCTGAGC	80176
rs186548291	snp	C/T	0.00318978	0.0398085	intron-variant	SPSB1	GRCh38.p7	1:9323828	TTCTTCTGCTGTTGC[C/T]CACGGACGGCAGGGG	80176
rs186588169	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291891	TAATCCTATTCTGAG[C/T]TCAAACAAAGCTAAA	80176
rs186620278	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9319783	TGGGGTGGCGGGGTG[A/G]CTGGTTCCATGAGCC	80176
rs186626304	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9355075	GGGTCGGGGGATGAG[A/C]CCCCCTTGCTGTCTG	80176
rs186766763	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9342317	CAACCCATGAGAAGA[A/G]GTTTGCGTAGTGACA	80176
rs186809930	snp	A/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9307319	TATATTCACAATGTC[A/G]TGCAACTATCCCCTC	80176
rs186855249	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9343921	CTCCCAAGTAGCTGG[A/G]ACTAGAGGCGCCTGC	80176
rs186948912	snp	C/T	0.00438332	0.0466095	intron-variant	SPSB1	GRCh38.p7	1:9366297	GGCATTTCCAGTTTC[C/T]TGGGGCCTGAGCTTG	80176
rs187060010	snp	A/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9344072	GGATTACAGGCGTGA[A/G]CCACCGCACCTGGCC	80176
rs187072042	snp	C/G/T	0.00914918	0.0670815	intron-variant	SPSB1	GRCh38.p7	1:9362297	GGCTCTCAGAGTTTG[C/G/T]GGGGGATAGGGGACC	80176
rs187086356	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9326204	GTGCTCATGAGAAGA[A/C]TTCTTCAATAACAAA	80176
rs187087966	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9295247	GTGTGTGTGTGCGCG[C/T]GTGCGGTTGGGGAGG	80176
rs187104153	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9346656	TGTGCAGTCTGGCCT[A/G]TCTCAGCCTCCCCCA	80176
rs187142546	snp	A/C/G	0.00795939	0.0626292	intron-variant	SPSB1	GRCh38.p7	1:9311295	GAGGCTGCGTCTGAG[A/C/G]CGAGTCCTGACCCAT	80176
rs187198606	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9346956	CTTGGGATAGATCAC[G/T]GTAGAAATAATGTCC	80176
rs187222034	snp	A/G	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9366067	ATCTGAGATGCAGCT[A/G]AATGAACTCAGCCTC	80176
rs187226380	snp	C/T	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9311347	CCTGATGGGTCTCGG[C/T]GTGGCTGAGGTTTTG	80176
rs187233637	snp	A/G	0.00318978	0.0398085	intron-variant	SPSB1	GRCh38.p7	1:9330598	TCCCTAACTTCACCC[A/G]ACACGTTTGGGGGAG	80176
rs187239953	snp	A/G	0.00716266	0.059414	intron-variant	SPSB1	GRCh38.p7	1:9299008	GGACTTGGAGGAGGC[A/G]GGGGTGGTGACCCCC	80176
rs187272061	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9308773	GTTGCAGGAAGTGGC[A/G]TGACTCCCTGGATGC	80176
rs187273198	snp	C/T	0.00914312	0.0669923	intron-variant	SPSB1	GRCh38.p7	1:9364847	TGTTGTTGTTGTTGT[C/T]GTTGTTGTTGTTGGT	80176
rs187305961	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9332792	TTGTTTTTTGGGCCC[A/G]TTCAATTTATCGATT	80176
rs187331885	snp	C/T	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9329775	AGACTTCCCAGATCT[C/T]GGCATCGGACACATG	80176
rs187460610	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9349681	CAGCATCGACTCTTC[A/G]ATCCAGATGAGATGC	80176
rs187487108	snp	A/T	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9351690	GAAGGAAGAGGACAG[A/T]TGGATGGCTTCAGTG	80176
rs187501515	snp	C/T	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9313666	ATGGGTGGGTGCTCC[C/T]GGGGAGGGGTCGAGT	80176
rs187506632	snp	A/G	0.255782	0.249933	intron-variant	SPSB1	GRCh38.p7	1:9293125	CGACCGGCCCGGGAG[A/G]GGGAGGCGCGGGGGG	80176
rs187518227	snp	A/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9316383	AGGGAGGGGCATGTG[A/T]GCACGTGTATTTATG	80176
rs187518374	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9334947	CTTTGTTCATCTGTC[C/T]GTGGACGCGGGTTGC	80176
rs187527628	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9302623	TACGAGTGGTCTCCG[C/G]AGTCTTTGACCTGGG	80176
rs187638168	snp	A/G	0.000106039	0.00728067	missense	SPSB1	GRCh38.p7	1:9356186	ACCCGTGGGCTGCAC[A/G]TGTGGCAGATCACGT	80176
rs187638548	snp	A/G	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9312396	AGGCAGTGAGCGCTA[A/G]CACAGGGTTCTTTCG	80176
rs187658136	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9299476	AGACGTCATCTCTCT[C/T]TCTCTCTCTCTCTTT	80176
rs187684038	snp	A/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9339403	GGACCCAGGGTCCTC[A/G]GGTAATTCCGGGGCG	80176
rs187687254	snp	A/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9321054	CTGGAAAAGGCAGCC[A/G]TGTAATTACAGGTAC	80176
rs187735409	snp	A/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9330753	AACCTAAAATTTACC[A/T]TCTTAACCATTTAAG	80176
rs187782479	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9299336	CTTGATCACCTTTCC[C/T]TTCCACAGATATCAT	80176
rs187796123	snp	A/G	0.00478085	0.0486577	intron-variant	SPSB1	GRCh38.p7	1:9316068	GTCAGGGAGGTGGTG[A/G]GTCCGCAGCGGCACA	80176
rs187814502	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9302469	AGGATCTGCCCTCCA[C/T]GTGGGCAGGCACCAT	80176
rs187910346	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9362567	CATTGCGGAAGCCGG[A/G]GCATTCTCTGATGCG	80176
rs188019406	snp	C/T	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9339737	TGTCTTCCCAGACCC[C/T]GAGTGACTGATGGCT	80176
rs188023514	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9306525	TCAAGTCATTCAGTC[A/G]TCATAATGTCCGTGA	80176
rs188038450	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9347025	TCCTTTATTTAAATA[A/C]CCTTCTGCCAGGCTG	80176
rs188048364	snp	C/T	0.00478085	0.0486577	intron-variant	SPSB1	GRCh38.p7	1:9311740	TTGCCGAGTGGTAGA[C/T]GTGAAACGTGGCTTT	80176
rs188169731	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9334231	GCTGGGATTACAGGC[A/G]CCCACCACGACACCT	80176
rs188185538	snp	A/G	0.0111196	0.0737302	intron-variant	SPSB1	GRCh38.p7	1:9293804	GGACGGGACGGCCCC[A/G]AGAGGAGGGTGCGGG	80176
rs188190087	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9301764	GACCTGGCTATGGCT[A/G]CCACTGGCTGCTAGT	80176
rs188268350	snp	C/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9357402	AGGTGGTCTTTGTTT[C/T]TCTGGGTGACCTGCC	80176
rs188275439	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9336805	ACTGCACTGCTCCCT[A/G]GAAAGAGGGGGACAC	80176
rs188290841	snp	A/C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9321213	AGAGGCGTCTCAGGC[A/C/G]GTGGGCCTTAAACAT	80176
rs188385642	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9364450	ACAAGTCCGGGCAGA[C/T]GGAGGGATGTGCTCC	80176
rs188399889	snp	C/G	0.00478085	0.0486577	intron-variant	SPSB1	GRCh38.p7	1:9328241	AATGGAATCTTGAAA[C/G]AGCTGAGCCCAAAGA	80176
rs188409326	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9357737	TGAATGCAGCCCATG[C/T]GTAGGGGCACCGTGC	80176
rs188413447	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9310462	CTTTGGGAGGCCGAG[A/G]CAGGCAGATCACTTG	80176
rs188414222	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9340329	GACTGGCCGGAGCCC[C/T]GCGGTCTGACTTTCA	80176
rs188418493	snp	A/G	0.00398564	0.0444627	intron-variant	SPSB1	GRCh38.p7	1:9345628	TCAGTCTGTTTGACT[A/G]TCATGCTGGTTTCCC	80176
rs188432471	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9297366	TCCAGGGTTGGAAAA[A/G]CCTACCTGTGACAAG	80176
rs188437056	snp	A/C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9321818	CACCGCAGAGACCAC[A/C/G]GGAGAGGCTCTTCAG	80176
rs188443183	snp	A/G	0.00914312	0.0669923	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291217	GTGAGACGGAGTCTC[A/G]CTCTGTCACCTGGGC	80176
rs188454805	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9306731	AGATAGGTCAGCAGA[A/G]TGAATGTCACTGTGG	80176
rs188526378	snp	C/T	0.0174175	0.0916809	intron-variant	SPSB1	GRCh38.p7	1:9361722	CTTGTGCTGAGGATG[C/T]AGCCAGAGAGGCTGC	80176
rs188558958	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9348485	GCCCTTCACCTGTCC[C/T]GGGTCTAGGACTCCC	80176
rs188563431	snp	A/G	0.00478085	0.0486577	intron-variant	SPSB1	GRCh38.p7	1:9312884	GGCCAGAGGCAGTGC[A/G]TGCCGATTGTCCAAA	80176
rs188567433	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291997	CTGGACAGCTGGCCT[C/T]GGGCCAGGCACTGTT	80176
rs188569401	snp	A/C/G	0.00199529	0.0315338	intron-variant	SPSB1	GRCh38.p7	1:9331552	GACCAGGCTGGTCTT[A/C/G]AACTCCTGACCTCAG	80176
rs188571760	snp	C/T	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9325873	TCAGGCCCGGTGTGC[C/T]CAGAGCCAGGCAGAG	80176
rs188577560	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9299669	TATTTAGTAGAGACA[A/G]GGTTTCACTATGTTG	80176
rs188673471	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9347859	CCTAGAAGGCTGCCC[C/T]AGTTCAGGGTCTGTC	80176
rs188800803	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9334463	TGGCCTCAAGTGATC[C/T]GCCTGCCTTGGCCTC	80176
rs188819320	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9343645	CTCCGGGCTCCTTTC[C/T]ACCTCTTTCCTGAGT	80176
rs188853837	snp	A/G	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9309129	TGTAGCAGGGAGGGC[A/G]TCAAATGCCAGGCCC	80176
rs188912479	snp	A/G/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9366403	TGACACCTTCAGGCC[A/G/T]TGGGGCCAGCCAGGC	80176
rs188916696	snp	A/G	0.00159617	0.0282053	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9368312	GGATATGTATGCCTC[A/G]CCCGCCCTCCCTGGG	80176
rs188935120	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9330980	CTAAATCTTTTATTG[A/G]AGGATGATATACCCA	80176
rs188970064	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9305849	ACAGGCCCGTCTCTG[C/T]TGATGATAGCGCTCA	80176
rs189085377	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9296577	CTTATGCTCACAGAA[C/G]ATGTGCACATGTGTA	80176
rs189096213	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9351411	GGAAATAAATGAAAG[C/T]GGAAATGCAATAACG	80176
rs189176766	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9337625	TGCTGAGGTGGGGTC[C/T]CCAGTTAGGTGCCTC	80176
rs189193239	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9354889	CAACCCAGAGTCCCT[A/G]TTCTCCCTCCTGAAG	80176
rs189314205	snp	A/G/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9300346	CTAGTTTTGAGTGGG[A/G/T]CCCGTAGCAGAAGAC	80176
rs189316443	snp	C/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9332570	AGACACTCCCTGGAG[C/T]CATGAGAGCAAAGGA	80176
rs189322934	snp	A/C	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9342081	GGTCTTGAGAAGCTC[A/C]TTCTAACCTGTCTTA	80176
rs189338255	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9358256	GGTCCTCTGCTGTGA[C/G]TTTGACTGTGATGGC	80176
rs189430208	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9352991	TACGCTGCAGGAAGC[A/G]TGACATGAACTAACT	80176
rs189466879	snp	A/C/T	0.00239393	0.0345281	intron-variant	SPSB1	GRCh38.p7	1:9344574	TCAGGTGTTGAGAGG[A/C/T]GGCAGGAGGAGGGCA	80176
rs189471063	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9317307	TGTCACTGGCGGAAG[A/G]TGGCATGTGTGTGCA	80176
rs189472675	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9318669	GTGTGGCTGGTGCCT[C/T]GGAGGCAGCTGTTTC	80176
rs189486372	snp	A/G	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9304104	AAAGCTGGAAGAAGG[A/G]CGAATCCTGGCTCTC	80176
rs189568736	snp	A/G	0.00716266	0.059414	intron-variant	SPSB1	GRCh38.p7	1:9349341	TTTGATATTGGTGAC[A/G]TGTCCTCTCCCTTTA	80176
rs189602125	snp	A/C	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9313359	GAGCCAAGATTGCAC[A/C]ACTGCACTCCAGCCT	80176
rs189680525	snp	G/T	0.000399281	0.0141238	utr-variant-5-prime	SPSB1	GRCh38.p7	1:9355760	AATACTGAACACTGC[G/T]CAGCTTGCAGAGGTC	80176
rs189685126	snp	A/G	0.00438332	0.0466095	intron-variant	SPSB1	GRCh38.p7	1:9320859	TGCGCCGGGTTTAGC[A/G]GGATGGAGTTAGAGT	80176
rs189689051	snp	A/G	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9338944	GACTCTGGAAAACCC[A/G]GCCGATTACCTTGTA	80176
rs189699691	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9305553	TGGATCCTAGCAGGG[C/T]CTGGGAGAGCTCGAT	80176
rs189738261	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9303127	GGACTACCAAGGGGA[A/C]ATTGATCTGGACTGC	80176
rs189798676	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9360609	GCCGGGAATCCTTGG[C/T]GTCCCTTGGTCTGTA	80176
rs189815143	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9324489	TGCCCAGCCTCTGGA[A/G]GGTCGGCTCGGAGGG	80176
rs189825838	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9308710	TAGATGTTACCTCCC[G/T]GTTTACAGATGAGAA	80176
rs189831906	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9342490	GCAGAAGGTAGGGCC[C/T]TTGCCAGTTTGGAGC	80176
rs189842794	snp	G/T	0.191461	0.24305	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9292749	CGCCCCGCGCCCCGC[G/T]CCCCCGGCCTTCCCT	80176
rs189986847	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9342324	TGAGAAGAGGTTTGC[A/G]TAGTGACAAGTCCAG	80176
rs190048477	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9346966	ATCACTGTAGAAATA[A/G]TGTCCCTCTTCGGGA	80176
rs190057087	snp	C/G	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9330607	TCACCCGACACGTTT[C/G]GGGGAGTATTTTGGG	80176
rs190068461	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9366171	CTCTGTAACCCTGGG[A/G]CCTGAGGCAGCTCTG	80176
rs190076720	snp	C/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9311382	GCTGTCTGCATTTAT[C/G]GAGATTTTTATAATG	80176
rs190118500	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9328020	TGCAATCACACTTAC[A/G]CTTTGGGAGGATTTC	80176
rs190126956	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9363254	TGTTTATGTACTTGA[C/G]GACCCAGAGAAGAGA	80176
rs190232633	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9323849	ACGGCAGGGGCTGTG[C/T]CATGTGGGACCTTGG	80176
rs190234544	snp	C/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9359421	AGGAGTGTCGTTCTG[C/T]GGCTGGGCGCGGTGG	80176
rs190273659	snp	C/T	0.0115144	0.0749975	intron-variant	SPSB1	GRCh38.p7	1:9322960	GGTTCCTGAATGGGC[C/T]TTGGAAATAGGTCAC	80176
rs190281923	snp	A/C	0.00119737	0.0244387	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291383	AGTAGTGACGGGTTT[A/C]ATCGTGTTAGCCAGG	80176
rs190385184	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9344999	TGGGTTTGGTCGGAT[C/T]CCCTATGTCCAAGAG	80176
rs190397619	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9310327	TAATTTCTGTGAGGG[A/G]AAAGGCATCTCATGT	80176
rs190416261	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9309706	AAATTAGTCGGGGAT[A/G]GTGGTGCATGCCCAT	80176
rs190515168	snp	C/G/T	0.00478085	0.0486577	intron-variant	SPSB1	GRCh38.p7	1:9307076	GGGATTACAGGCACG[C/G/T]GCCACCACGCCTGGC	80176
rs190587552	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9350617	GCGTGCATGCGTGTG[C/T]GTGGTGGGTGGCGGT	80176
rs190595373	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9333944	CACATTCCTTCTCAT[C/T]TTTTTGCTTTTGTCC	80176
rs190618576	snp	C/G/T	0.00517822	0.0506191	intron-variant	SPSB1	GRCh38.p7	1:9315275	TGCGACAAAAGACCC[C/G/T]GTACTGGCTCCAAGG	80176
rs190647275	snp	C/G	0.00358779	0.0422022	intron-variant	SPSB1	GRCh38.p7	1:9326547	CCCTGGTGGACTGGT[C/G]GGGGAGGGCTTGGTT	80176
rs190684894	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9296186	TCATGGTTTCACGGT[A/G]CGTGCGAGTACTGGC	80176
rs190701058	snp	A/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9361341	CCTGATCTGGGGCTT[A/T]GCTGTCTCTGTCTTG	80176
rs190735173	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9311330	GGGGTTTCTTTCTTC[C/G]CCCTGATGGGTCTCG	80176
rs190743534	snp	C/G	0.00318978	0.0398085	intron-variant	SPSB1	GRCh38.p7	1:9346632	CATCGGGGGGTTGCC[C/G]GCAGGTGCTGTGCAG	80176
rs190750535	snp	C/G	0.00318978	0.0398085	intron-variant	SPSB1	GRCh38.p7	1:9330121	GTGGCGTAAATAATT[C/G]CTAGGTGCTTGCTCA	80176
rs190776340	snp	G/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9310796	TTCTCCTGTCTGAGG[G/T]TCTTCTCATTTGGAG	80176
rs190858402	snp	A/G	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9334270	TTTGTATTTTTAGTA[A/G]AGACGGGATTTCACC	80176
rs190883378	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9301890	TTTGGAAGGGGCAGC[A/G]TTTTGTCCTTACTGG	80176
rs190887579	snp	A/G	0.00478085	0.0486577	intron-variant	SPSB1	GRCh38.p7	1:9313873	CTCCTGCTTTTCCCT[A/G]TAGGAGTGAACAAGA	80176
rs190898329	snp	C/T	0.00279162	0.0372561	intron-variant	SPSB1	GRCh38.p7	1:9332803	GCCCGTTCAATTTAT[C/T]GATTAGGAGGTCATG	80176
rs190900148	snp	C/T	0.00557542	0.0525036	intron-variant	SPSB1	GRCh38.p7	1:9300880	GTTCCCTCTGATCGA[C/T]TGACAGTGGAAGAGA	80176
rs190982898	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9364638	TCCTCCATTCGTCTC[A/C]AATCAGAGCTCCTCT	80176
rs191019796	snp	C/T	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9319955	CCCTGAGCTGGCCAC[C/T]TGCAGGCCTGGTCCC	80176
rs191021558	snp	A/G	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9355126	AAGAATGTAGCTGGC[A/G]GAGGAGGCTCCTGGT	80176
rs191024694	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9329614	CAGGAGAATCCCTTG[A/G]ACCAGGATGGGGAGG	80176
rs191124213	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9351156	AGTTTTATTGAAACA[C/T]ATTCATGCCCATTGA	80176
rs191139379	snp	A/G/T	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9315804	ATTCTCTTTGCAAAC[A/G/T]GTTCAGTTTCACATG	80176
rs191253084	snp	G/T	0.00279162	0.0372561	intron-variant	SPSB1	GRCh38.p7	1:9338309	CCCCTGCCCAGGGGA[G/T]ACCCTGTCCCCAGGG	80176
rs191279610	snp	A/G	0.0138799	0.0821421	intron-variant	SPSB1	GRCh38.p7	1:9305140	TCCCTCTCCTCCCTT[A/G]TAGCCTCAGCCACTG	80176
rs191333593	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9341405	GGGTGTTGCCTGCCT[C/T]CCCCCACTAGACTGA	80176
rs191349898	snp	C/T	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9357962	ACTGTCCTTAAAGGG[C/T]AGGTTCAGCTCAGCA	80176
rs191353874	snp	A/G	0.0134861	0.0810011	intron-variant	SPSB1	GRCh38.p7	1:9307073	GCTGGGATTACAGGC[A/G]CGTGCCACCACGCCT	80176
rs191362809	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9321846	CAGTGGCAGAAGTAT[C/G]TTGGGTGGTGTTTTA	80176
rs191371176	snp	G/T			upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291320	CCTCCCAAGTAGCTG[G/T]GACTTACAGATGCCC	80176
rs191481322	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9344150	TCATTTAATAGGGAT[C/T]TGAGATTCTAAACTG	80176
rs191495883	snp	A/T	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9362350	GGATCTCAGGCGTCC[A/T]TCCCCAGTTGACAAG	80176
rs191503898	snp	A/G	0.031825	0.122064	intron-variant	SPSB1	GRCh38.p7	1:9309438	TCTTCCCACCTCAGC[A/G]TCCTGAGTAGCGGGA	80176
rs191513956	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9326330	CACTGGAGGTGGAGA[C/T]ACCCAGGGGCCACTC	80176
rs191517597	snp	C/T	0.00398564	0.0444627	intron-variant	SPSB1	GRCh38.p7	1:9295864	CTGGTGTGCATGACT[C/T]AGTGTATCTTTTGGT	80176
rs191632230	snp	A/G	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9306533	TTCAGTCGTCATAAT[A/G]TCCGTGATACCTATA	80176
rs191641661	snp	C/T	0.00159617	0.0282053	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291074	CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATCG	80176
rs191647833	snp	A/G	0.0142736	0.0832652	intron-variant	SPSB1	GRCh38.p7	1:9299040	CCACATCCCCATTCA[A/G]CTCTCCGATTTGGCC	80176
rs191687280	snp	C/T	0.00557542	0.0525036	intron-variant	SPSB1	GRCh38.p7	1:9364850	TGTTGTTGTTGTCGT[C/T]GTTGTTGTTGGTTTT	80176
rs191717725	snp	C/G	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9304612	TGGGGTGTAGAGAAG[C/G]GTGAAGAATTGCAGG	80176
rs191764217	snp	C/T	0.0111196	0.0737302	intron-variant	SPSB1	GRCh38.p7	1:9362035	TTTGGTGTGGTTTGT[C/T]GTGGTTGAAGGTTCA	80176
rs191815204	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9350408	GCGCGGTCCTGGGGA[C/T]GTGGTGACTAATGCA	80176
rs191832430	snp	A/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9324714	CAGCCAGCATCTCCC[A/G]GAGCCCAGAATCTCT	80176
rs191838451	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9293148	GCGGGGGGCCGGGCG[A/G]GGGCGGACGCGGGGA	80176
rs191848028	snp	A/G	0.00755907	0.0610114	intron-variant	SPSB1	GRCh38.p7	1:9301537	GGAAGATGTATGTGG[A/G]TAGACCTGAGTGCGC	80176
rs191962979	snp	A/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9346684	CCAGGGTCTGCTCTC[A/G]GTGCCTCATTCCTCC	80176
rs191998824	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9351873	CAGATGGCAGAAGTG[A/G]CCGGGTGTGTGGGCC	80176
rs192035608	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9335045	CTGCTTTGCATTTAT[C/T]TGAGTGAACACCCAG	80176
rs192122756	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9294763	ACTTCATTTCTCATC[A/G]TGGGGTGTGAGGAGA	80176
rs192125588	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9343242	TCATCACCCCTAAAA[C/G]AAACCTCTGTCACTT	80176
rs192129441	snp	C/T	0	0	intron-variant	SPSB1	GRCh38.p7	1:9308963	AGGAAACATGAGCTC[C/T]CTGCCAGGGGCTGGG	80176
rs192130846	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9309257	TTCCTGTGTGCTCCC[C/T]TGCGGAGAGAGAGAG	80176
rs192147002	snp	C/T	0.00517822	0.0506191	intron-variant	SPSB1	GRCh38.p7	1:9331111	GCTCTCCCCGCTGAA[C/T]GCTTGTGGAAGTGTC	80176
rs192153528	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9356962	AGTGGTTGAACAAAC[A/G]GATGGATGGATGTGG	80176
rs192162478	snp	A/T	0.00279162	0.0372561	intron-variant	SPSB1	GRCh38.p7	1:9312426	GTAACAGCCCTGTGG[A/T]GGTATTATGCACACG	80176
rs192175591	snp	C/T	0.02016	0.0983543	intron-variant	SPSB1	GRCh38.p7	1:9299548	GCAATGGTGCAATCT[C/T]GGCTCACTGCAACCT	80176
rs192267764	snp	A/G	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9347690	AGCTCCGTGGTGTAG[A/G]TGAGGTGGGACTCAT	80176
rs192276609	snp	A/G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9311835	GCATCCCTGGGGGGT[A/G/T]TGAATTTTCTTGGTG	80176
rs192306089	snp	A/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9297780	ATAGGCTTAGGTTTC[A/T]TGTAGAGTTAGGGAT	80176
rs192310558	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9351471	GAGTTTTAGGTAAGT[A/G]TGTGACAGACAAACG	80176
rs192313891	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9316361	GAGAGACAGCCCCTG[G/T]GGCACAAGGGAGGGG	80176
rs192321755	snp	C/T	0.00318978	0.0398085	intron-variant	SPSB1	GRCh38.p7	1:9334766	ATGGATCCGATTGTC[C/T]TAGGTACCTCATGTA	80176
rs192331005	snp	A/C/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9302605	TTTGGACTCTGGGAC[A/C/T]CGTACGAGTGGTCTC	80176
rs192526761	snp	A/C	0.00318978	0.0398085	intron-variant	SPSB1	GRCh38.p7	1:9321246	ACATTCTTGGGGCTT[A/C]GCTGACTCCTTCGAG	80176
rs192661919	snp	C/T	0.00478085	0.0486577	intron-variant	SPSB1	GRCh38.p7	1:9330794	CAGTAGCGTTGAGTA[C/T]ATTACCGGATCGTAC	80176
rs192671166	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9366312	CTGGGGCCTGAGCTT[A/G]GCCTGGGCCCTCAGC	80176
rs192678831	snp	A/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9299362	ATCATACTGGGGCTG[A/G]GCACGGTGGCTCACT	80176
rs192723737	snp	A/T	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9353340	CTTCCCTCCCGCAGC[A/T]TGAGGCGCAGGCCCC	80176
rs192794600	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9357443	ATCCTCAGTTGACCA[A/G]ATTCTAGCCCAGTTG	80176
rs192871503	snp	C/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9343846	GCTGGAGTGCAGTGG[C/T]GCGATCTCGGCTCAC	80176
rs192876783	snp	C/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9316853	CTCCTATGACCTGGC[C/T]GGACCTTGTGACCTC	80176
rs192921640	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9366853	TGCTGGGATTACCAG[C/T]GTGAACCACCATGCC	80176
rs192947164	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9306455	AGTGGGGTCAGTGAC[A/G]ATAGCCATCAACGAT	80176
rs192948201	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9339476	GAGGCCAACCAGGGA[A/C]GGCTCCGTGGAGGAG	80176
rs193004838	snp	A/G	0	0	intron-variant	SPSB1	GRCh38.p7	1:9340188	CTGTTCTCAAGAGAG[A/G]AGACAGACTCTCCTT	80176
rs193013443	snp	A/G	0.00953873	0.0683987	intron-variant	SPSB1	GRCh38.p7	1:9296192	TTTCACGGTGCGTGC[A/G]AGTACTGGCTCTGAT	80176
rs193079461	snp	G/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9302681	CCTGAAGCAGCTGAC[G/T]TGAAAGAAGGGCAGT	80176
rs193104477	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9326072	CACCCCTGCATGTCC[C/T]TTAGTTCATCTGTCC	80176
rs193148117	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9327118	AAGAGACTAGCACAA[C/T]CCCCAGTGCCCACTT	80176
rs193150895	snp	A/G	0.00755907	0.0610114	intron-variant	SPSB1	GRCh38.p7	1:9362827	GCTCCCAGAAATAGC[A/G]CCTGATTGACTTCCT	80176
rs193179236	snp	G/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9321072	TAATTACAGGTACTG[G/T]AAATAGTCCTGTTTC	80176
rs193205928	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9309876	GAGTAGAATAAAATA[A/G]TGGTAACTGGGGGCC	80176
rs193297138	snp	A/C	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9344595	GAGGAGGGCAGGGAG[A/C]AGCATGTATGAAGCT	80176
rs199573556	in-del	-/T	0.0158469	0.0875917	intron-variant	SPSB1	GRCh38.p7	1:9313398	AGAGCGAAACACCGC[-/T]CTTCATTTTCTATAA	80176
rs199662217	in-del	-/GAAC			intron-variant	SPSB1	GRCh38.p7	1:9298404	AATGAATGAATGAGT[-/GAAC]GAATGAATGAATAAG	80176
rs199751640	snp	A/G	8.26467e-05	0.00642779	missense	SPSB1	GRCh38.p7	1:9355974	AGCAGGAGCTCCAGG[A/G]TCTGGATTACTGCAA	80176
rs199887072	in-del	-/GT			intron-variant	SPSB1	GRCh38.p7	1:9309280	AGAGAGAGAGAGAGA[-/GT]GTGAGAGAGAGAGAG	80176
rs199887402	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9349913	GACGGTCCTGCAGTT[A/G]GAGCTCCTGTACATA	80176
rs199889254	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9306930	TTTTCTTCTTTTCTT[C/T]TTTTTTTTTTTTTTT	80176
rs199938330	in-del	-/AGC	0.48435	0.0870631	intron-variant	SPSB1	GRCh38.p7	1:9330473	CTGTCTCAAAATAAT[-/AGC]AACAATAATAATAAT	80176
rs199970373	snp	C/T	3.4901e-05	0.00417723	synonymous-codon	SPSB1	GRCh38.p7	1:9356146	GGCCCAGAGCACGGA[C/T]GCTATCAGGGGCAAA	80176
rs200011127	in-del	-/CT			intron-variant	SPSB1	GRCh38.p7	1:9324505	GGTCGGCTCGGAGGG[-/CT]GTGGGCCCGGGACTC	80176
rs200026656	snp	A/G	0.494526	0.0520291	intron-variant	SPSB1	GRCh38.p7	1:9357149	TGGATGGATGGATGG[A/G]TGGATGGATGGGTGG	80176
rs200090150	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9357269	TGGATGAGTGGGTAG[A/G]TGGATGGATGGATGG	80176
rs200100319	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9295241	GTGTGTGTGTGTGTG[C/T]GCGCGCGTGCGGTTG	80176
rs200210190	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9365567	GTGGCCTCTTGCGTG[A/G]TGAGATGTAGGAAAC	80176
rs200211088	in-del	-/CTTC			intron-variant	SPSB1	GRCh38.p7	1:9306927	TACTTTTCTTCTTTT[-/CTTC]TTTTTTTTTTTTTTT	80176
rs200251006	snp	A/G	9.95239e-05	0.00705351	missense	SPSB1	GRCh38.p7	1:9356496	TGGGAGTGGCTTTTC[A/G]GGGACTCAAGGGCAA	80176
rs200272075	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9330473	TCTGTCTCAAAATAA[C/T]AACAATAATAATAAT	80176
rs200284654	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9330855	TGTGTCCAGCGGCTG[G/T]GCCATTTTGCGTTTC	80176
rs200360673	in-del	-/TGAATGAG			intron-variant	SPSB1	GRCh38.p7	1:9298379	GCCCCCATGAATGAA[-/TGAATGAG]TGAATGAATGAATGA	80176
rs200427907	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9310364	CTTGGGGCGCCTTCC[C/T]GGATTTCTAAGGGAT	80176
rs200461720	in-del	-/CTT			upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291172	CAGGCTGGTCCTGAA[-/CTT]CTTCTTTTTTTTTTT	80176
rs200478229	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9331289	CTGTCATAAATACCC[G/T]TTATGGATCTCCTTC	80176
rs200528637	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9342523	CCTCAGGGTGTTGAC[C/T]TGCTCAGTGAGAAAG	80176
rs200530330	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9296607	ACACACACATACATA[A/T]GCACACACATATATG	80176
rs200587981	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9294102	TATGTCTGTGTGTCT[G/T]TGTGTGTGTCTGTGT	80176
rs200635541	in-del	-/TGTG			intron-variant	SPSB1	GRCh38.p7	1:9348938	TCACTCGTGCAAGAA[-/TGTG]TGTGTGTGTGTGTGT	80176
rs200653520	snp	C/T	0.000443328	0.0148818	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9367580	TCTACCAGTGACGTT[C/T]GCCATCATACCGCCA	80176
rs200658561	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9314188	CTCAAAAAAAAAAAA[G/T]AAAAAACAAAAAAAA	80176
rs200659889	snp	G/T			utr-variant-3-prime	SPSB1	GRCh38.p7	1:9369448	AGAGCCTTGTGGCTT[G/T]TACAGTTTTGAAACT	80176
rs200660299	in-del	-/T			intron-variant	SPSB1	GRCh38.p7	1:9306931	TTTCTTCTTTTCTTC[-/T]TTTTTTTTTTTTTTT	80176
rs200662059	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9330560	GTCCAGATCACAAGG[G/T]CCAGCTGGCAGGATG	80176
rs200703828	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9335005	GCTGCTATGAACATG[A/G]GTGCACAAATATCTG	80176
rs200739926	in-del	-/TGAA			intron-variant	SPSB1	GRCh38.p7	1:9357214	GGGTGGATGGATCAG[-/TGAA]TGAATGGATGGATGG	80176
rs200766488	in-del	-/GA			intron-variant	SPSB1	GRCh38.p7	1:9309334	TGTGTGTGTGTGTGT[-/GA]GTGACAGATTCTCTC	80176
rs200825779	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9357271	GATGAGTGGGTAGAT[A/G]GATGGATGGATGGAT	80176
rs200987869	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9357161	TGGGTGGATGGATGG[A/G]TGGATGGATGGGTGG	80176
rs201092066	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9321439	AACTTGTCCTGACCC[A/G]TTATTCGTCACCTTG	80176
rs201124393	in-del	-/ATGA	0.185155	0.241444	intron-variant	SPSB1	GRCh38.p7	1:9298369	CACAACTAAGCCCCC[-/ATGA]ATGAATGAATGAATG	80176
rs201125330	in-del	-/G	0.0185938	0.0946107	intron-variant	SPSB1	GRCh38.p7	1:9325155	ACTGGGCTTCCCCCA[-/G]GCCGGGGCGCTGGGC	80176
rs201185309	snp	C/T	0.00207815	0.0321677	intron-variant	SPSB1	GRCh38.p7	1:9367428	AGCTGCGCTGACCTG[C/T]AGTTTCTCTGTCTCC	80176
rs201212630	in-del	-/GCA			intron-variant	SPSB1	GRCh38.p7	1:9330474	TGTCTCAAAATAATA[-/GCA]ACAATAATAATAATA	80176
rs201233051	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9306925	TTTACTTTTCTTCTT[C/T]TCTTCTTTTTTTTTT	80176
rs201236473	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9347419	AAAGGAATACATGCA[A/T]TTTAAAAAATTCAAT	80176
rs201248098	in-del	-/TTG			intron-variant	SPSB1	GRCh38.p7	1:9364820	AGTTTTGGGGTTTTT[-/TTG]TTGTTGTTTTGTTGT	80176
rs201263557	in-del	-/G			intron-variant	SPSB1	GRCh38.p7	1:9336656	GCTGCCTGAGTTCAC[-/G]CCGTGGCGCTGGGCT	80176
rs201360994	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9359848	GCCAGGATGGAAGCC[A/G]GGGGGGTGGGTGGCG	80176
rs201375535	snp	A/G	1.64762e-05	0.00287016	missense	SPSB1	GRCh38.p7	1:9356399	CTGGAACCAGATGAG[A/G]CATTCATTGTCCCTG	80176
rs201389836	in-del	-/TC	0.482979	0.0906686	intron-variant	SPSB1	GRCh38.p7	1:9306929	CTTTTCTTCTTTTCT[-/TC]TTTTTTTTTTTTTTT	80176
rs201430237	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9294103	ATGTCTGTGTGTCTT[A/T]GTGTGTGTCTGTGTG	80176
rs201449650	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9343990	AGATGGGGTTTCACC[A/G]TGTTAGCCAGGATGG	80176
rs201457778	in-del	-/C			intron-variant	SPSB1	GRCh38.p7	1:9320917	TGGGGAGGGGCCAAA[-/C]CCCCTCCCCCTGCCA	80176
rs201558017	in-del	-/CTCT			intron-variant	SPSB1	GRCh38.p7	1:9299469	TCTCTCTCTCTCTCT[-/CTCT]TTTTTTGAGATGGAT	80176
rs201679038	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9306927	TACTTTTCTTCTTTT[C/T]TTCTTTTTTTTTTTT	80176
rs201734491	in-del	-/T/TTTTTTTTA	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9311616	CTCTTATCTCTAGGC[-/T/TTTTTTTTA]TTTTTTTTATGGGGC	80176
rs201735753	in-del	-/TGT			intron-variant	SPSB1	GRCh38.p7	1:9364831	TGTTGTTGTTGTTGT[-/TGT]CGTTGTTGTTGTTGG	80176
rs201765185	in-del	-/TGGATGGATGGATGGATGGATGAGTGGA			intron-variant	SPSB1	GRCh38.p7	1:9357090	GGATGGATGGGTGGG[-/TGGATGGATGGATGGATGGATGAGTGGA]TGGATGGATGGATGA	80176
rs201812930	snp	A/C/T	4.94828e-05	0.00497387	synonymous-codon	SPSB1	GRCh38.p7	1:9356032	CATGCCCCCTGTGTC[A/C/T]TATGATGTCCAGCTG	80176
rs201876405	snp	G/T	0.0021232	0.0325129	intron-variant	SPSB1	GRCh38.p7	1:9356598	ATCGTAAGTGTCTCC[G/T]CTGCTGTCAGAGGCA	80176
rs202052843	in-del	-/T	0.00755907	0.0610114	intron-variant	SPSB1	GRCh38.p7	1:9354868	ATGCAGTGAGATCTC[-/T]TCCCCCAACCCAGAG	80176
rs202055543	in-del	-/TGAATGAATAAG	0.316	0.241131	intron-variant	SPSB1	GRCh38.p7	1:9298431	GAATAAGTGAACGAA[-/TGAATGAATAAG]TGAATGAATAAGTGA	80176
rs202062401	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9314195	AAAAAAAACAAAAAA[A/C]AAAAAAAACAGTGAA	80176
rs202167879	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9296605	GTACACACACATACA[C/T]ATGCACACACATATA	80176
rs202191600	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9330472	TTCTGTCTCAAAATA[A/G]TAACAATAATAATAA	80176
rs202196379	snp	C/T	8.72684e-05	0.00660504	synonymous-codon	SPSB1	GRCh38.p7	1:9356230	GCGGGGCACACACGC[C/T]GTGGTGGGGGTGGCG	80176
rs202229587	in-del	-/G			intron-variant	SPSB1	GRCh38.p7	1:9325238	CCACCCCCCCCCCCC[-/G]CCCCGCCTCCACCGG	80176
rs367561369	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9294030	AGACTCTAAGTGACT[C/G]TGTGTGTGTGTGTGT	80176
rs367646325	snp	A/G	0.00318978	0.0398085	intron-variant	SPSB1	GRCh38.p7	1:9349554	TCTCTGACACAAGGC[A/G]TGCAGGAGCGTGGGT	80176
rs367685793	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9331288	TCTGTCATAAATACC[C/G]GTTATGGATCTCCTT	80176
rs367740286	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9328622	GTGTTGGGGTGAGCA[C/T]CAACGCCCCACCCAC	80176
rs367759143	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9301906	TTTTGTCCTTACTGG[A/G]GCAGGCACTTATTCT	80176
rs367805814	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9332424	ATCTGGGTGAACTAG[A/G]GGTTGATGATAGAAA	80176
rs367807361	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9345132	GAGCGAGGCCCTTCC[A/G]GAGAACCAGCTTCTC	80176
rs367811686	snp	A/G	0.000980002	0.0221143	intron-variant	SPSB1	GRCh38.p7	1:9356633	CCTCCCTCAGTCCCC[A/G]TGGTCCTGGCTGGGC	80176
rs367839714	snp	A/G	0.00318978	0.0398085	intron-variant	SPSB1	GRCh38.p7	1:9359763	TGGATGGCAGAGGCA[A/G]GAGTGGCCTCTGAGA	80176
rs367854687	snp	C/T			utr-variant-5-prime	SPSB1	GRCh38.p7	1:9355759	CAATACTGAACACTG[C/T]GCAGCTTGCAGAGGT	80176
rs367892247	snp	C/T	0.00755907	0.0610114	intron-variant	SPSB1	GRCh38.p7	1:9361843	TGCCCGCCACCCTCC[C/T]TGGAGATGTGGAAAG	80176
rs367893327	snp	C/T	1.69055e-05	0.00290731	synonymous-codon	SPSB1	GRCh38.p7	1:9356260	GACGGCAGACGCCCC[C/T]CTGCACTCTGTCGGG	80176
rs367955900	snp	A/G	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9316953	GCTCTCCTTCTGATC[A/G]CAGAGATCCCAGGCC	80176
rs367976239	snp	C/T	0.0138799	0.0821421	intron-variant	SPSB1	GRCh38.p7	1:9328653	TGCCTCCCTCTGGCC[C/T]GGGAGAGCCATGGAG	80176
rs367986696	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9299565	GCTCACTGCAACCTC[C/T]GCCTCCCGGGTTCAA	80176
rs367994929	in-del	-/TTATTC			intron-variant	SPSB1	GRCh38.p7	1:9344679	CTGCCCTTCTTATTC[-/TTATTC]CCCCAGGTGGTTTGA	80176
rs368008074	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9336308	TCTCGGCTCACTGCA[A/G]CCTCTGCCTCCGAGT	80176
rs368059849	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9323177	GGGGTATCCATGGGG[C/T]CTCTGTCCCGGCACT	80176
rs368085051	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9353334	CTCCCCCTTCCCTCC[C/T]GCAGCTTGAGGCGCA	80176
rs368094751	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9321572	AGAGACTGATGAGTC[A/G]GTGAGGGAGACCGAT	80176
rs368116035	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9310303	AGATTCACAGGATTC[A/G]GACAACGGTAATTTC	80176
rs368121681	snp	C/G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9313261	AAAAAGTAGCCAGAC[C/G/T]TGGTGCCGGGCACCT	80176
rs368165985	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9314921	AACAGCATGTCCTGC[A/G]CACAGGAGTGGCCTC	80176
rs368210749	snp	A/G	0.00517822	0.0506191	intron-variant	SPSB1	GRCh38.p7	1:9299313	GTCACAGTTTAGTTC[A/G]CAGTCATCTTGATCA	80176
rs368356313	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9301760	AGCCGACCTGGCTAT[A/G]GCTACCACTGGCTGC	80176
rs368470499	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9307389	CCCCATCCACATTCG[A/G]CGTCACCTCCCATCC	80176
rs368526697	snp	C/T	0.00438332	0.0466095	intron-variant	SPSB1	GRCh38.p7	1:9309173	GGGCATGGGGTGTCC[C/T]TGCACTTCCATGCCA	80176
rs368584693	in-del	-/ATTATT			upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291585	CCAATTATTATTATT[-/ATTATT]TAATTTTTGTGCAGA	80176
rs368654441	snp	C/T	7.0553e-05	0.00593898	synonymous-codon	SPSB1	GRCh38.p7	1:9356164	TATCAGGGGCAAAGT[C/T]GGGTATACCCGTGGG	80176
rs368684339	snp	G/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9348886	AAACACTGGGTTGAG[G/T]GCTTTTGCCGTCAAA	80176
rs368719006	snp	A/C			upstream-variant-2KB	SPSB1	GRCh38.p7	1:9292392	CCGTCCCCGTGGGCA[A/C]CGAAACGCGAGCGGC	80176
rs368754125	in-del	C/TT			intron-variant	SPSB1	GRCh38.p7	1:9306939	TTTCTTCTTTTTTTT[C/TT]TTTTTTAAGTGGAAT	80176
rs368891918	in-del	-/CT			intron-variant	SPSB1	GRCh38.p7	1:9294115	TTTGTGTGTGTCTGT[-/CT]GTGTGAGTGTGTATG	80176
rs368908744	snp	G/T	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9313761	CAGTCCAGCCTGCCC[G/T]CTGTGCTTCAGTGGC	80176
rs368923185	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9318997	GCCTGGGCAACATGG[C/T]GAAACCTGTCTCTAC	80176
rs368977739	snp	A/G	0.00318978	0.0398085	intron-variant	SPSB1	GRCh38.p7	1:9353833	ATAGGCAGGAGAATC[A/G]CTTGAACCCAGGAAG	80176
rs369083166	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9299348	TCCCTTCCACAGATA[C/T]CATACTGGGGCTGGG	80176
rs369100322	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9352537	CTGGCCCTCAAAGCC[A/T]GGCATTTACTATCGC	80176
rs369109030	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9334229	TAGCTGGGATTACAG[A/G]CGCCCACCACGACAC	80176
rs369112320	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9318080	GTTGGGGAAACGCAG[C/T]GATTGTTCTGGGAAG	80176
rs369146415	snp	A/G	0.031825	0.122064	intron-variant	SPSB1	GRCh38.p7	1:9309453	ATCCTGAGTAGCGGG[A/G]ATTATAGGTATGTGT	80176
rs369192172	in-del	-/AAATA			intron-variant	SPSB1	GRCh38.p7	1:9313418	ATTTTCTATAAAATG[-/AAATA]AAATAAAATAAAATA	80176
rs369249392	snp	A/G	1.65228e-05	0.00287422	synonymous-codon	SPSB1	GRCh38.p7	1:9356323	CTGGGGCTGGGACTT[A/G]GGGCGCAACCGGCTC	80176
rs369296072	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9319404	CTTCTCCTCCCTCCT[C/T]CCTCCTCCTTCCTCC	80176
rs369321807	snp	C/T	0.000147472	0.00858581	intron-variant	SPSB1	GRCh38.p7	1:9356623	GAGGCAATGCCCTCC[C/T]TCAGTCCCCATGGTC	80176
rs369324091	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9305941	GTGTGGCCAAAATGA[A/G]TGCAGAGAGGCAGGA	80176
rs369374290	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9362783	ATGTGGAAGCTGGTG[C/T]ACTGTCTCTTCCAGT	80176
rs369388591	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9318875	AGGAGTCCAGCCTGC[A/G]GTGTCCTGCAGTGAG	80176
rs369409883	in-del	-/TG			intron-variant	SPSB1	GRCh38.p7	1:9296610	ACACATACATATGCA[-/TG]CACACATATATGCAC	80176
rs369470511	snp	G/T	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9310679	CAGCCTGGGCAATGG[G/T]AGTTAGACCTTGTCT	80176
rs369530409	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9340448	GAAAACGTGGGTCCC[A/G]GAGGTTTGTTTTGTT	80176
rs369661087	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9294112	TGTCTTTGTGTGTGT[C/G]TGTGTGTGAGTGTGT	80176
rs369701535	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9332834	ATCTTGGAAGAGCAT[A/T]TTCCCTGCAGGGTCT	80176
rs369713101	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9349545	GACAGCTGATCTCTG[A/C]CACAAGGCGTGCAGG	80176
rs369721097	in-del	-/T			intron-variant	SPSB1	GRCh38.p7	1:9358920	AGGTGCAGACACATG[-/T]CCTGTGAATAGGCGA	80176
rs369729474	in-del	-/GTGT			intron-variant	SPSB1	GRCh38.p7	1:9294044	TGTGTGTGTGTGTGT[-/GTGT]CTGAGTGCGTCTTTG	80176
rs369750114	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9317191	AGGGTTTACTCTCAG[C/G]AGGTGAATCTGGGAA	80176
rs369778131	in-del	-/TGGGGG			intron-variant	SPSB1	GRCh38.p7	1:9360211	TAGAGGCCAGGAGGG[-/TGGGGG]CTGAAGGGACCCAGT	80176
rs369785692	snp	C/G	0.00914312	0.0669923	intron-variant	SPSB1	GRCh38.p7	1:9354382	TTCAACGGGAGCCTG[C/G]CTTGCCCCTGGCCTA	80176
rs369811778	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9302877	ATGGGAGTGGCACTG[C/G]GCATCATATCCCCTA	80176
rs369852354	in-del	-/CT			intron-variant	SPSB1	GRCh38.p7	1:9307623	GTGGGATGGAAGAGT[-/CT]GATCCAAACAGCTTG	80176
rs369922808	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9349197	AGGTGACTCCAGGGC[A/C]CGTGGCTGCTCTCCG	80176
rs369922967	snp	A/G	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9353895	TGCACTCCAGCCTGG[A/G]CAACAAGAGCAAAAC	80176
rs369954209	snp	A/T	1.64765e-05	0.00287019	missense	SPSB1	GRCh38.p7	1:9356424	TCCCTGACTCCTTCC[A/T]GGTAGCCCTGGACAT	80176
rs369979219	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9339973	TTTCCTCCAGCCCCC[A/C]ACCTCGGGAGGACCC	80176
rs370001085	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9361694	TTCCTCCTCAAGGCT[C/G]GAGGCACAAGGCCTT	80176
rs370024240	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9314006	CATGGTGAAATCCCT[G/T]TTCCACTAAAAATAC	80176
rs370097632	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9338215	TCCCCTACCCCGTTT[A/C]TTCAGGCTTCTGCTC	80176
rs370150261	snp	C/G/T	1.7159e-05	0.00292903	synonymous-codon, missense	SPSB1	GRCh38.p7	1:9356125	CATCTTTCACCGGCA[C/G/T]CCGGTGGCCCAGAGC	80176
rs370177134	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9309231	TGCAGATAAGCTAGA[C/T]CCCCCCTCAATTCCT	80176
rs370206762	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9319953	GCCCCTGAGCTGGCC[A/C]CCTGCAGGCCTGGTC	80176
rs370294351	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9315545	AATGTGAATGTGACT[A/C]CTGAGCTGCAGCTTC	80176
rs370303216	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9294974	AGGCCCAGAGAGGGC[A/G]GTTCACTTACCCAGA	80176
rs370388555	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9359558	AATGCAAAAATTAGC[C/T]GGGCGTGGTGGCATG	80176
rs370439572	in-del	-/GTGT			intron-variant	SPSB1	GRCh38.p7	1:9348961	TGTGTGTGTGTGTGT[-/GTGT]ATATGTGCGTGTGTG	80176
rs370511966	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9364172	AGCCCCTCCACTTTC[C/T]GGCGGGGGCTGAGCC	80176
rs370542194	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9321200	TAGTTTAGTCTGCAG[A/G]GGCGTCTCAGGCGGT	80176
rs370544293	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9359328	GTGATAGGGTGAGGC[A/G]CGGGTGTTAGCGCTG	80176
rs370556018	snp	A/G	0.00012551	0.00792081	utr-variant-5-prime	SPSB1	GRCh38.p7	1:9355888	GGTGAAGCCAGGGGC[A/G]AACATGGGTCAGAAG	80176
rs370558554	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9314896	CAGGGAGAGGACTGC[C/G]GCAAAGGAGAACAGC	80176
rs370636037	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9337756	CTGGTAAGGATGAAC[C/T]TCCCTGCTCCCTGCC	80176
rs370657469	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9333756	CCAACGGAAAGGAAA[C/T]GAGGTTGCCAAAGAG	80176
rs370695170	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9338879	TGGGTCTTGGGGAGG[G/T]TGCAGCAGCCACAGA	80176
rs370713280	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9367247	GTTAGCAGAGGGCTC[A/G]CCCAGGTGCCCAGCC	80176
rs370722109	in-del	-/G	0.0298908	0.118541	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291540	GCCTCCCAAAGCGCT[-/G]GGATTACAGGTGTGA	80176
rs370765541	snp	G/T	0.00597247	0.0543191	intron-variant	SPSB1	GRCh38.p7	1:9309118	CTGCAGAGCTGTGTA[G/T]CAGGGAGGGCATCAA	80176
rs370775724	in-del	-/AGTCAC			intron-variant	SPSB1	GRCh38.p7	1:9325569	CACCGTGGAACAGAC[-/AGTCAC]TCAGCAGGCATGTAT	80176
rs370850231	in-del	-/AAAA			intron-variant	SPSB1	GRCh38.p7	1:9329719	CAAAAAAAAAAAAAA[-/AAAA]GAGAAAAGAAAGAAA	80176
rs370865050	in-del	-/TGAATGAATGAG			intron-variant	SPSB1	GRCh38.p7	1:9298375	CTAAGCCCCCATGAA[-/TGAATGAATGAG]TGAATGAATGAATGA	80176
rs370902009	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9335560	ACGCCTGTAATCCCA[A/G]CACTTCGGGATTCCA	80176
rs370909891	snp	A/G	1.76089e-05	0.00296718	missense	SPSB1	GRCh38.p7	1:9356211	TCACGTGGGCCATGA[A/G]ACAGCGGGGCACACA	80176
rs370953652	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9337598	CAGCTGTGAGTGCAG[C/T]GCCTCCAGCCTTGCT	80176
rs370994931	snp	C/G	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9312321	CACGAGCCATTGTGT[C/G]CGGTCTGTCTGGTTT	80176
rs371018916	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9355594	GGGATTTCATTCTGC[A/G]CCAAGGCTCCAGCCT	80176
rs371103665	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9331178	AATTGCTGTGTAACA[A/G]CGGTTCATGGTGCAA	80176
rs371115598	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9305093	CCACTTCTCCCTCTC[A/G]CCCTTGTGGCCCATC	80176
rs371160367	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9326110	GGTGGCTGGGCTGCC[A/G]ACACGTGGGGAGGTC	80176
rs371181090	snp	C/T	0.0123036	0.0774623	intron-variant	SPSB1	GRCh38.p7	1:9358103	TGCAGCTTCTCCTCC[C/T]GGAGAAGGAGGTCCT	80176
rs371284980	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9317383	GATAAAAGTCATCAC[C/T]GAAATCAATCTGACT	80176
rs371287376	snp	A/G	0.031825	0.122064	intron-variant	SPSB1	GRCh38.p7	1:9309450	AGCATCCTGAGTAGC[A/G]GGAATTATAGGTATG	80176
rs371301085	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9294312	AGTGCGTCTGTGTAT[A/G]TGTGAGTGTCTGTGT	80176
rs371365012	in-del	-/G	0.02016	0.0983543	intron-variant	SPSB1	GRCh38.p7	1:9348969	TGTGTGTGTGTATAT[-/G]TGCGTGTGTGCACGT	80176
rs371377006	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9345207	CTGCCTCAAGCCCCC[A/G]TCTCCTGCCTTCTGG	80176
rs371428445	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9360580	CCCCATGCCTCCCCT[C/T]GCCCCTGGGGGCTGC	80176
rs371449237	in-del	-/G			intron-variant	SPSB1	GRCh38.p7	1:9338729	TGAGGTCTGAGGGGG[-/G]CGTCACCTCCCCCAT	80176
rs371536331	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9355077	GTCGGGGGATGAGCC[C/T]CCCTTGCTGTCTGAA	80176
rs371555692	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9368162	ACCCATCCTGGCTGC[C/T]GGTGCCCCGTACCCT	80176
rs371612690	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9301979	GTCACCATCCATTGA[C/T]TGACAGAACACCTTT	80176
rs371633005	snp	C/T	0.00318978	0.0398085	intron-variant	SPSB1	GRCh38.p7	1:9367097	TAGCTGCATCTCCTG[C/T]CAGCAGGGCGACCCC	80176
rs371674641	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9317152	AGGTGCTTAGAGGCC[A/G]GCAAGGTTCTGGCCT	80176
rs371698743	snp	A/G	0.0123036	0.0774623	intron-variant	SPSB1	GRCh38.p7	1:9358429	CGGGGAAGTCACCTC[A/G]GAAATGGAACCAGCA	80176
rs371727652	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9302292	GTAGATGGTAAAGCA[C/T]TGATTATTCTCTATG	80176
rs371904919	in-del	-/TGGG			intron-variant	SPSB1	GRCh38.p7	1:9357146	GAGTGGATGGATGGA[-/TGGG]TGGATGGATGGGTGG	80176
rs371938005	in-del	-/AC			intron-variant	SPSB1	GRCh38.p7	1:9296617	CATATGCACACACAT[-/AC]ATATGCACACATACA	80176
rs371948497	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9346456	CCAGTCGCTTTGGCT[A/G]CATCCCCAAAAGAGG	80176
rs371952034	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9365993	CGCGCAGCCTTCCAA[C/T]GCTCAGAAGCCTTGG	80176
rs371957324	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9319125	GGCAGAGGTTGCAGT[A/G]AGCCAAGATCACACC	80176
rs371962195	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9323202	GGCACTCAGCCTTTT[C/T]GCTCTCACGAAGTGC	80176
rs371970475	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9344995	AGCCTGGGTTTGGTC[A/G]GATCCCCTATGTCCA	80176
rs372054088	snp	A/G	0.00358779	0.0422022	intron-variant	SPSB1	GRCh38.p7	1:9349982	AGGTACACGTGTGTC[A/G]TGTCTGCCTGTGTCT	80176
rs372073961	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9302904	CCTAGGGACCCGCTA[A/G]CGAAATTGTTGCTTC	80176
rs372151217	snp	C/T	0.00279162	0.0372561	intron-variant	SPSB1	GRCh38.p7	1:9320644	GGAGAAACTGACTTG[C/T]CCCAAATCTCTGATC	80176
rs372154604	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9353182	TCTGACCTCGAGAGC[C/T]GCCTCAGCCCGCCCG	80176
rs372159966	in-del	-/CTCCTCC			intron-variant	SPSB1	GRCh38.p7	1:9319392	TCAGGTGCTTTGCTT[-/CTCCTCC]CTCCTCCCTCCTCCT	80176
rs372190869	snp	C/T	0.00755907	0.0610114	intron-variant	SPSB1	GRCh38.p7	1:9299711	CTTGAACTCCTGACA[C/T]CAAGTGATTCACCCG	80176
rs372225362	in-del	-/TGCTGGTGGTGGCCC			intron-variant	SPSB1	GRCh38.p7	1:9345939	ACGTGTCACAAGCCC[-/TGCTGGTGGTGGCCC]CTTTGCCAGGGGCTC	80176
rs372291258	in-del	-/A			intron-variant	SPSB1	GRCh38.p7	1:9311625	CTAGGCTTTTTTTTA[-/A]TGGGGCAGGGGAGCA	80176
rs372326853	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9342429	GGCCCCAGCGTCAAC[C/T]GTGGGAGAGCACGGA	80176
rs372335482	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9328493	GCCTTAAGAATCCGT[C/T]AAGGCCACTTCGGGG	80176
rs372342143	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9299425	AGGAGGATCGCTTGA[A/G]CTTAGGAGTTTGAGA	80176
rs372375508	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9307577	GAAGCTGGATTTCCC[A/G]TCCTGGCTCAGTTGT	80176
rs372405560	in-del	-/CCT			intron-variant	SPSB1	GRCh38.p7	1:9343364	TCGTACAATGTGTGA[-/CCT]TTTATATCTGGCTTC	80176
rs372422051	snp	A/G	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9355734	GTTGTTTGTCTTTCC[A/G]TCCATTAGGCAATAC	80176
rs372454440	in-del	-/GCGA			intron-variant	SPSB1	GRCh38.p7	1:9343366	TACAATGTGTGACCT[-/GCGA]TTTATATCTGGCTTC	80176
rs372459874	in-del	GGG/T			intron-variant	SPSB1	GRCh38.p7	1:9313581	ATGTGAATTCTGGGA[GGG/T]GTGGGCCCGGGCTGC	80176
rs372659333	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9364033	GGTTGATTGGAAACC[C/T]GTTACACCAAGAGGG	80176
rs372691340	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9311532	GGAAAGACCGATCGG[G/T]CTTAGAAATAGCATC	80176
rs372829355	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9296629	ACATATATGCACACA[C/T]ACACACACACGCTGG	80176
rs372887775	in-del	-/TG			intron-variant	SPSB1	GRCh38.p7	1:9293985	CTCTGAGTGTGTGTG[-/TG]AGTCTGTGTGTCTGT	80176
rs372895383	snp	A/G	1.84497e-05	0.00303719	intron-variant	SPSB1	GRCh38.p7	1:9356626	GCAATGCCCTCCCTC[A/G]GTCCCCATGGTCCTG	80176
rs372941737	snp	C/T	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9315254	AACCAGCTCAGCAGA[C/T]TCCACTGCGACAAAA	80176
rs372944699	snp	C/G/T			intron-variant	SPSB1	GRCh38.p7	1:9360596	GCCCCTGGGGGCTGC[C/G/T]GGGAATCCTTGGCGT	80176
rs372947811	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9334160	GTGCGATCTCGGCTC[A/G]TTGCAACTTCCGCCT	80176
rs372997486	snp	C/T	5.01341e-05	0.00500645	synonymous-codon	SPSB1	GRCh38.p7	1:9355954	CCCCACGTACAGGCC[C/T]CTGAAGCAGGAGCTC	80176
rs373004063	in-del	-/T			intron-variant	SPSB1	GRCh38.p7	1:9306930	TTTCTTCTTTTCTTC[-/T]TTTTTTTTTTTTTTT	80176
rs373035704	in-del	-/GTGAGAGAGAGA			intron-variant	SPSB1	GRCh38.p7	1:9309282	AGAGAGAGAGAGAGT[-/GTGAGAGAGAGA]GAGAGAGAGTGTGTG	80176
rs373061807	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9334577	TTAGGTACCTTCATA[C/T]TGTTGTACAACCATC	80176
rs373118886	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9329991	AGTGGCCCAGGAGCA[A/G]GTGACTGCACATTTT	80176
rs373126493	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9343676	ATGCCGATACAGTTT[G/T]TTCTAGGTTTTAGTC	80176
rs373130925	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9329300	GGTGGATGGGTGGAC[A/G]GGTGGACAGGCGGAT	80176
rs373148421	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9314501	TCTACACAACAAGGC[A/C]GTTCATCACCAAATG	80176
rs373216222	snp	C/T	0.00279162	0.0372561	intron-variant	SPSB1	GRCh38.p7	1:9314241	ATACCCCCAAATATC[C/T]ACCTGACATTTTCAG	80176
rs373274521	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9358970	TGCATGAGATGGGAG[A/G]TTGGATGCTTTCATA	80176
rs373276786	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9354845	CAGTGGAGAGGGATC[A/G]GGTAGATGATGCAGT	80176
rs373281878	in-del	-/C			intron-variant	SPSB1	GRCh38.p7	1:9324627	TCCCTGAGGCTGAAA[-/C]CTGCCAGTGGCCAGC	80176
rs373288178	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9321262	GCTGACTCCTTCGAG[C/T]GTCGAGTTTCTGGGT	80176
rs373336392	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9359862	CGGGGGGGTGGGTGG[C/G]GGGGGCGGCCCGGTT	80176
rs373377237	snp	A/G	0.00795532	0.062565	intron-variant	SPSB1	GRCh38.p7	1:9366599	TTTTTTTTTTGGACC[A/G]AGTCTTGCTCTGTCG	80176
rs373444806	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9323073	GGTGGACGGGCCAGG[C/T]GGCCGCCCCTCCCCA	80176
rs373490373	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9364762	GACCGTCCATGGGGG[A/G]TGAAGAGCAGTGGTC	80176
rs373503553	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9337656	TCTGGGGGTGGCATC[C/T]GCTCAGAGCCTCAGG	80176
rs373505803	snp	A/G/T	5.18285e-05	0.00509039	synonymous-codon	SPSB1	GRCh38.p7	1:9356245	CGTGGTGGGGGTGGC[A/G/T]ACGGCAGACGCCCCC	80176
rs373548222	snp	C/T	6.91718e-05	0.00588057	missense	SPSB1	GRCh38.p7	1:9356564	TGTGAGATCCGAATG[C/T]GCTACTTGAACGGAC	80176
rs373627505	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9334148	TGGAGTGCGGTGGTG[C/T]GATCTCGGCTCGTTG	80176
rs373630088	snp	A/G/T			intron-variant	SPSB1	GRCh38.p7	1:9300483	GGCAGGCCCCTGTAG[A/G/T]TGAATCGCAGTACAG	80176
rs373636701	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9297972	ACAGTGGGAGCCGCA[G/T]TCACTCAAATGGAAA	80176
rs373725193	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9332317	TGAGAGTGAAGGTGG[A/G]ATTCAGCAACTATGG	80176
rs373749107	in-del	A/GC			intron-variant	SPSB1	GRCh38.p7	1:9309230	GTGCAGATAAGCTAG[A/GC]TCCCCCCTCAATTCC	80176
rs373783064	snp	C/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9301476	GCCTGGGCAACAGAA[C/T]GAGACCCTGTATCAA	80176
rs374078576	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9335818	GTCTGTGAAAAAAAG[A/G]AAGAAAGAATGTTGT	80176
rs374128268	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9298410	TGAATGAGTGAACGA[A/G]TGAATGAATAAGTGA	80176
rs374165716	snp	C/T	0.00358779	0.0422022	intron-variant	SPSB1	GRCh38.p7	1:9336433	GTTTCTCCACGTTGG[C/T]CAGGCTGGTCTCAAA	80176
rs374191404	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9318629	TTACCTTGCGGAATC[A/G]TGCAGGATTGACCAA	80176
rs374203854	snp	G/T	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9363525	CTCAGACCTTGGACC[G/T]GTAACTCTCACCTCC	80176
rs374348508	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9293834	GTCTGCAGGAAGAGC[A/G]GGTGTCTCTGAGAGT	80176
rs374406481	snp	A/G	0.00279776	0.0372968	intron-variant	SPSB1	GRCh38.p7	1:9332228	GAGCGTTTTAGGAAG[A/G]TTTGTTTGAGTGGGC	80176
rs374496306	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9351976	CCTGCCCTGCCCGGG[G/T]AAAACGCCCCACCCT	80176
rs374504954	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9331105	TGTCGTGCTCTCCCC[A/G]CTGAATGCTTGTGGA	80176
rs374517340	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9308980	TGCCAGGGGCTGGGC[A/G]GGCACCAGGCCTGCG	80176
rs374626561	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9322623	GTTGCGGACAGAGGT[A/G]GGAGGTGGTGTGGGG	80176
rs374629970	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9344023	TCGATCTCCTGACCT[C/T]GTGATCCGCCCACCT	80176
rs374695255	snp	C/T	0.00438332	0.0466095	intron-variant	SPSB1	GRCh38.p7	1:9310910	AATTTATTCCAATTC[C/T]GTAATATATAAATTA	80176
rs374705322	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9314770	TGGCAAGTGGCTGAG[C/G]TTGTACCCCTAAATA	80176
rs374742418	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9358541	GGCTGCAGATTGGGA[A/G]CCCTGGGCATATCCT	80176
rs374766298	snp	A/G	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9299629	GGATTACAGGCATGC[A/G]CCACCACACCCAGCT	80176
rs374766668	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9295924	AGGTCAGGTACAGGT[G/T]TGCCTCAGTCTGCCC	80176
rs374790645	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9329093	AGATGTGTAGGAGTT[C/T]GCGTGGGGGACAGGG	80176
rs374836513	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9340852	TCTGCCCAGCAAGGC[A/G]AGCACATGAAACGCA	80176
rs374846608	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9325251	CCGCCCCGCCTCCAC[C/T]GGTGCAGATGGAGAG	80176
rs374880370	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9319693	CCTGCTCGTCTGGCC[C/T]GGCCAGATCTGCAGT	80176
rs374989098	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9322547	GAGGGATGGCAATCA[C/T]GATGAGGGCTCAGGG	80176
rs375015240	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9347802	TGGGTGATTGCTGGG[C/T]GTTTTGCACATGGAC	80176
rs375019976	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9368534	TCTTGGGCTCAGGCA[C/G]CCTTGCACAGGGTTG	80176
rs375050328	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9348091	CTGGGATTACAGGTG[C/T]TCACCACCACGCCCA	80176
rs375086439	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9360515	GGCCAGGTGTCTGCG[A/C]TCAGGATGGTAGCGG	80176
rs375109143	in-del	-/AAACA			intron-variant	SPSB1	GRCh38.p7	1:9315892	AAACAAAACAAAACA[-/AAACA]TGGAGTTTTCTTTCC	80176
rs375196146	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9315859	GTGGATTTGTTTCAT[G/T]TAAGGGGAAAACAAA	80176
rs375215572	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9366676	TCTCCCAGGTTCAAG[C/T]GATTCTCCTGCCTCA	80176
rs375223438	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9349716	GTCTTCCGTGACTCA[C/T]GGCCTCTGGGCCAGT	80176
rs375247676	in-del	-/TGGG			intron-variant	SPSB1	GRCh38.p7	1:9357158	GGATGGGTGGATGGA[-/TGGG]TGGATGGATGGGTGG	80176
rs375262962	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9299225	CAGCAGAAGCAGTTT[A/G]CATCCAGCTGGTAAG	80176
rs375287923	in-del	-/GCCGGG	0.00119737	0.0244387	cds-indel	SPSB1	GRCh38.p7	1:9292957	GCTCCAGGCGCCGGC[-/GCCGGG]GCCGGGGCCGCGGGG	80176
rs375360131	snp	A/G	0.0107246	0.0724382	intron-variant	SPSB1	GRCh38.p7	1:9336620	AAGGAAGAGTCTGGG[A/G]CAGAGGCAGGGGCAG	80176
rs375360285	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9309421	CTCCTGGGCTCAAGC[C/G]ATCTTCCCACCTCAG	80176
rs375425434	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9309232	GCAGATAAGCTAGAT[C/T]CCCCCTCAATTCCTG	80176
rs375427938	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9316833	TTCCACCTCGGTTCT[C/T]CCTGCTCCTATGACC	80176
rs375435202	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9296521	AGGTTTCCTCACCTC[A/G]CATGCACACACATAC	80176
rs375437707	snp	A/G	0.00716266	0.059414	intron-variant	SPSB1	GRCh38.p7	1:9323101	CCAGCTCCGGCCTTC[A/G]AGGACTTTGCGGCCT	80176
rs375460868	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9355621	GCCTGCCCGTGTCAG[A/G]CATGACAGAGCCCAG	80176
rs375466914	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9331215	CAGAGTGGTCTGCCT[A/G]AGTGACCTTTGTCAA	80176
rs375503571	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9344892	GTGACCCAAGGACCA[C/G]TCCCAGAGGTGACCT	80176
rs375555731	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9329153	TTGAAGACACCTAAG[A/G]GCAGTTGTATGAAGC	80176
rs375561812	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9302748	GTGACAATACTTTGT[A/T]GGGCTGGGTCAGGGG	80176
rs375584237	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9312509	ATGTGGTCAGGCAGC[C/T]GTGGACACCGTCCTA	80176
rs375587504	snp	A/G			upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291818	AAACCGCTGGCACCT[A/G]GAAAGTCAGAATGCC	80176
rs375622360	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9344078	CAGGCGTGAGCCACC[A/G]CACCTGGCCAAGATA	80176
rs375700527	snp	A/C	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9314181	ACTCTATCTCAAAAA[A/C]AAAAAACAAAAAACA	80176
rs375711883	snp	A/C	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9317326	CATGTGTGTGCAAAA[A/C]CACTGGGAGCTTTGA	80176
rs375774977	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9364137	GGAGCTTTCTCAGGT[A/G]CTTTCCAGCCACGAG	80176
rs375813211	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9317630	ATGCACTACCACGCC[C/T]AGATATATATATATT	80176
rs375814702	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9343496	TACCACAATTTGTTT[A/G]TCCATGCATCCATTG	80176
rs375968461	snp	A/G			utr-variant-3-prime	SPSB1	GRCh38.p7	1:9369095	TTTTAAACAGCTGCT[A/G]TAGAGTACCTTTTTT	80176
rs376015206	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9332813	TTTATCGATTAGGAG[A/G]TCATGATCTTGGAAG	80176
rs376018852	in-del	-/TGTG			intron-variant	SPSB1	GRCh38.p7	1:9348960	GTGTGTGTGTGTGTG[-/TGTG]TATATGTGCGTGTGT	80176
rs376060720	in-del	-/TTCC			intron-variant	SPSB1	GRCh38.p7	1:9362210	TCCTTCCTTCCTTCC[-/TTCC]ATGTCGGGGAGGGGT	80176
rs376081968	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9330310	CCGTCTCTACTAAAA[A/G]TACAAAATACAAAAT	80176
rs376085384	snp	A/G	6.95955e-05	0.00589855	synonymous-codon	SPSB1	GRCh38.p7	1:9356143	GGTGGCCCAGAGCAC[A/G]GACGCTATCAGGGGC	80176
rs376115158	in-del	-/ACCATGTTTCTAG			intron-variant	SPSB1	GRCh38.p7	1:9337021	GGCATCTGGCTGCAG[-/ACCATGTTTCTAG]CTCTCTCTGGCATCA	80176
rs376196553	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9318257	GCAGCAGAACAGTGA[C/T]GGGTCCTCCGCCCGC	80176
rs376278962	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9349226	CGGCTCTGAGGGTCC[A/G]GGCCATGGTTCCTGC	80176
rs376290536	snp	A/G			upstream-variant-2KB	SPSB1	GRCh38.p7	1:9292529	AACCCCACTCTCCGC[A/G]AAGATTTCTCCTTCT	80176
rs376347816	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9362974	AGGTGCCCACCCCCT[C/T]GGTAGATTTCAGCAG	80176
rs376422421	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9319318	TGTGGACATGTGTGC[A/G]CTGCCCTGGCCGTGG	80176
rs376423233	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9337522	ACAGGGTGAGGCTGG[A/G]GGTAGGGGAGGGGTG	80176
rs376509397	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9350506	CTGCCTGGACTATGA[A/C]GCCTCTGTCCTGCTT	80176
rs376527670	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9364779	GAAGAGCAGTGGTCC[C/T]TCTTCTTTTGTTTAT	80176
rs376538176	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9308735	TGAGAAAGGAGGACT[C/T]TTTTTTTAGAGAGGT	80176
rs376543426	snp	A/G	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9337740	GGAGGCTGCAGAGCC[A/G]CTGGTAAGGATGAAC	80176
rs376665013	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9305583	TGTGGGCCCAGGGTG[G/T]GGGTGCTGGGGGTGG	80176
rs376757109	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9329527	ACACAATGAAACCCC[A/G]TCTCTACAAAAAATG	80176
rs376771202	in-del	-/CAAACG			intron-variant	SPSB1	GRCh38.p7	1:9296604	GTACACACACATACA[-/CAAACG]TATGCACACACATAT	80176
rs376784592	snp	A/G	0.00398564	0.0444627	intron-variant	SPSB1	GRCh38.p7	1:9323757	GGTCCTACAGGCCTC[A/G]GTGAGACAGTGCTAT	80176
rs376851691	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9297683	TTTGGTTGGCTGACT[A/G]GAACATGGATCAAAG	80176
rs376871513	in-del	-/GT			intron-variant	SPSB1	GRCh38.p7	1:9294126	TCTGTGTGTGAGTGT[-/GT]ATGTGTCTTTGGGTG	80176
rs376879513	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9351917	AGGCCCTGGGGTGCC[A/C]TTGTGAAGGAATCAC	80176
rs376892340	snp	C/T	0.00358779	0.0422022	intron-variant	SPSB1	GRCh38.p7	1:9306111	TGCAGCGGGAGGAAC[C/T]GAGACATGGGGGTTG	80176
rs376917255	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9299428	AGGATCGCTTGAACT[C/T]AGGAGTTTGAGACCA	80176
rs376930630	snp	A/C	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9344137	ATCCTGATGGTTTTC[A/C]TTTAATAGGGATCTG	80176
rs376958125	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9320877	ATGGAGTTAGAGTGA[A/G]CTCTGGCCACGAAAG	80176
rs376997295	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9319666	GTGCAGAGGATGCTG[C/T]GGGAGGCCAAGCCTG	80176
rs377006664	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9313626	TTCTGATGGAGAGAA[A/G]CCTTAGCCAGGCAAA	80176
rs377014407	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9353195	GCCGCCTCAGCCCGC[C/T]CGGCCCCTCGAGAGC	80176
rs377086028	in-del	-/C	0.00199481	0.0315187	downstream-variant-500B	SPSB1	GRCh38.p7	1:9369973	TTGTGTCCCCTGGGG[-/C]TGAGTGCACGGTGAT	80176
rs377105623	snp	C/T	0.0115144	0.0749975	intron-variant	SPSB1	GRCh38.p7	1:9361582	CTTCTACACTGGGGC[C/T]GTGGCCGGGCGGAAG	80176
rs377154058	snp	C/G	1.79657e-05	0.00299709	utr-variant-5-prime	SPSB1	GRCh38.p7	1:9355887	AGGTGAAGCCAGGGG[C/G]GAACATGGGTCAGAA	80176
rs377186103	snp	A/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9294767	CATTTCTCATCGTGG[A/G]GTGTGAGGAGAACAG	80176
rs377243114	snp	A/G			utr-variant-3-prime	SPSB1	GRCh38.p7	1:9367630	CCAACTCACTGAGCC[A/G]CCTGCCGCTGGGGCC	80176
rs377277962	in-del	-/GGAT			intron-variant	SPSB1	GRCh38.p7	1:9357242	GATGGATGGATGGAT[-/GGAT]AAATGAACAGGTGGA	80176
rs377405031	snp	A/C/T	1.64972e-05	0.00287199	synonymous-codon	SPSB1	GRCh38.p7	1:9356041	GGTGGCCCAGAGCA[A/C/T]	80176
rs377429641	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9359356	CTGCCAGCCTCAACC[C/T]GCTTAACCCGACACC	80176
rs377460219	snp	C/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9307921	TCCTCGCCATGGTCC[C/G]CCTCAACTGTGATGC	80176
rs377495023	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9358554	GAGCCCTGGGCATAT[C/T]CTGCCTAGGACCTAG	80176
rs377623107	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9335530	AGATCGTTGTGGGGT[C/T]GGGTGCAGTGGCTCA	80176
rs377656001	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9330559	ACATCCTGCCAGCTG[A/G]ACCTTGTGATCTGGA	80176
rs377713915	snp	A/G	1.67565e-05	0.00289447	missense	SPSB1	GRCh38.p7	1:9367511	CCCTGGGGAGGGAGC[A/G]CCTGGGGGAGATCCA	80176
rs377719657	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9364255	AGGCCAGATGCAGGC[A/G]CGCTCCCAAGCAGAG	80176
rs377720143	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9318065	CCCCTTTCCGGGCAG[A/G]TTGGGGAAACGCAGC	80176
rs377720706	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9350712	ACGCCCTTTGCGTCT[C/G]CTCCTCCTGGGTGGG	80176
rs377723314	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9318631	ACCTTGCGGAATCGT[C/G]CAGGATTGACCAAAG	80176
rs386628321	in-del	AGAGTGTGA/T			intron-variant	SPSB1	GRCh38.p7	1:9295209	GTGTGTGTGTGTGTG[AGAGTGTGA/T]GTGTGTGTGTGTGTG	80176
rs386628322	in-del	ATG/GTGAACGAATGAATGAATA			intron-variant	SPSB1	GRCh38.p7	1:9298402	TGAATGAATGAATGA[ATG/GTGAACGAATGAATGAATA]AGTGAACGAATGAAT	80176
rs386628323	multinucleotide-polymorphism	CCGT/TCCA			intron-variant	SPSB1	GRCh38.p7	1:9302026	CCGTGTAGCACTGCT[CCGT/TCCA]GGGAGCTCACTTCAC	80176
rs386628324	in-del	CTTC/TTCTTCTT			intron-variant	SPSB1	GRCh38.p7	1:9306925	TTTACTTTTCTTCTT[CTTC/TTCTTCTT]TTTTTTTTTTTTTTA	80176
rs386628325	multinucleotide-polymorphism	CGT/TGA			intron-variant	SPSB1	GRCh38.p7	1:9307074	CTGGGATTACAGGCA[CGT/TGA]GCCACCACGCCTGGC	80176
rs386628326	in-del	AGTGTGAGAGAGAGA/TGT			intron-variant	SPSB1	GRCh38.p7	1:9309279	GAGAGAGAGAGAGAG[AGTGTGAGAGAGAGA/TGT]GAGAGAGAGTGTGTG	80176
rs386628327	multinucleotide-polymorphism	CC/TT			intron-variant	SPSB1	GRCh38.p7	1:9320976	CTTAAAATCTCCTTC[CC/TT]GAGTCCCTGGCTGCC	80176
rs386628328	multinucleotide-polymorphism	CCG/GCC			intron-variant	SPSB1	GRCh38.p7	1:9336657	GCTGCCTGAGTTCAC[CCG/GCC]TGGCGCTGGGCTAGT	80176
rs386628329	multinucleotide-polymorphism	GGG/TGT			intron-variant	SPSB1	GRCh38.p7	1:9342459	AGGATCCCAGTGGCT[GGG/TGT]CAATTCGCTGATAGC	80176
rs386628330	in-del	ACCT/CGA			intron-variant	SPSB1	GRCh38.p7	1:9343363	ATCGTACAATGTGTG[ACCT/CGA]TTTATATCTGGCTTC	80176
rs386628331	multinucleotide-polymorphism	AGG/CGT			intron-variant	SPSB1	GRCh38.p7	1:9348224	TGCTGGGATTACAGG[AGG/CGT]GAGCCACCGCGGCAA	80176
rs386628332	in-del	A/GTGTGTGTG			intron-variant	SPSB1	GRCh38.p7	1:9348955	TGTGTGTGTGTGTGT[A/GTGTGTGTG]TATATGTGCGTGTGT	80176
rs386628333	in-del	A/GTGTGTG			intron-variant	SPSB1	GRCh38.p7	1:9348957	TGTGTGTGTGTGTGT[A/GTGTGTG]TATATGTGCGTGTGT	80176
rs386628334	in-del	ATATAT/GTGTGTGTATATG			intron-variant	SPSB1	GRCh38.p7	1:9348957	TGTGTGTGTGTGTGT[ATATAT/GTGTGTGTATATG]TGCGTGTGTGCACGT	80176
rs386628335	in-del	-/A/GTGTG			intron-variant	SPSB1	GRCh38.p7	1:9348959	TGTGTGTGTGTGTGT[-/A/GTGTG]TATATGTGCGTGTGT	80176
rs386628336	multinucleotide-polymorphism	GTT/TTG			intron-variant	SPSB1	GRCh38.p7	1:9364828	GGTTTTTTTGTTGTT[GTT/TTG]TTGTTGTTGTTGTTG	80176
rs397816441	in-del	-/A			intron-variant	SPSB1	GRCh38.p7	1:9314187	CTCAAAAAAAAAAAA[-/A]CAAAAAACAAAAAAA	80176
rs397832282	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9298416	agtgaacgaatgaat[A/G]agtgaacgaatgaat	80176
rs397979138	in-del	-/A	0	0	intron-variant	SPSB1	GRCh38.p7	1:9335899	ACCCTCCGAATGTCA[-/A]TGTGCACAGTAGTAA	80176
rs397979139	in-del	-/G	0	0	intron-variant	SPSB1	GRCh38.p7	1:9352963	TGAGCGGCAGGGGGG[-/G]CTGTGGAGGGGCTAC	80176
rs398089120	in-del	-/T			intron-variant	SPSB1	GRCh38.p7	1:9340002	CCCACCGACAGCCCT[-/T]GAACCACCTGGGCAT	80176
rs527241237	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9359327	GGTGATAGGGTGAGG[C/T]GCGGGTGTTAGCGCT	80176
rs527318596	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9321545	AGCTCAGAACGGGGA[A/G]GAGGGTGTTTGAGAG	80176
rs527342197	snp	C/T	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9349590	GACGGCTTGCCTGCC[C/T]TCCTCAGGAGGAAGC	80176
rs527358097	snp	A/T	0	0	intron-variant	SPSB1	GRCh38.p7	1:9332488	TTGAGTCTACAAGGG[A/T]TGTATGAGTGGGAGC	80176
rs527426613	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9358804	GTTTGCACAGCTTCA[C/T]GGTTATGTATCATAG	80176
rs527442712	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9297131	GAGATGTGACTGTGA[A/G]AATGGTTTGTCAACA	80176
rs527484649	snp	A/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9296442	CATTTTTTTAGTGAA[A/T]TTTTTTGTTATTATG	80176
rs527518671	in-del	-/CT			intron-variant	SPSB1	GRCh38.p7	1:9348368	TGTATCCAGAAGGCG[-/CT]CTCTGACCACAGGGA	80176
rs527529804	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9331821	TGCAACGTGCGATCT[C/T]ATTACTGCTTTTCTT	80176
rs527551297	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9342705	CTGGGGCACACATCC[A/G]AGATGCAGGCACACA	80176
rs527575124	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9306162	TTGACCCCACAGGGC[A/C]GGGACTGAGGGCACC	80176
rs527612784	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9306447	CTGTCTATAGTGGGG[C/T]CAGTGACAATAGCCA	80176
rs527618436	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9301269	CCAAGGTGGGAGGAT[C/T]GCTTGAGCCCAAGGA	80176
rs527645258	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9365080	CAGGCTGGTCTTGAA[C/T]TCCTGCCCTCAGGTA	80176
rs527648915	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9297999	GAAAACTTAAATGCA[A/G]CGGGAGTAATTGCAT	80176
rs527668737	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9353052	CCAGGGAGCTGACCT[A/C]TGTGCCCACAGGACC	80176
rs527671736	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9333225	CTTCCTGGACAGCAG[A/C]CTGTCCCTAATTCTT	80176
rs527705252	snp	A/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9365595	AACAATTTTAGAACA[A/T]TTTCATCACCCCAAA	80176
rs527809994	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9302495	ACCATCCAGTCAGCC[A/G]GGGGCCTGGAAGAAG	80176
rs527834078	snp	C/T	0.00676609	0.0577691	intron-variant	SPSB1	GRCh38.p7	1:9307013	GCTCACTGCAGCCTC[C/T]GCCTCCCAGGTTCCA	80176
rs527897971	snp	A/G	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9343761	CTTGTGCTCTTGTAC[A/G]GAGATCCTTCCCATT	80176
rs527976598	in-del	-/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9335872	GGCTGGACGATGATC[-/T]TTGGAGTTTTTACCC	80176
rs528003836	snp	C/T	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9316826	GCTGGCTTTCCACCT[C/T]GGTTCTCCCTGCTCC	80176
rs528005903	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9297717	GACCCACTGTGAGTA[A/G]GTTGGAGTTTCTGGG	80176
rs528024406	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9348653	GAGGTTCTTTTCTTC[C/T]TTCCTACTAAGATCT	80176
rs528048022	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9305432	AGGAGGGCAGGACCC[A/G]GCCGGCCACATGGCT	80176
rs528057513	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9335809	CAGGACCCTGTCTGT[C/G]AAAAAAAGAAAGAAA	80176
rs528059147	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9367173	ATGGGGATGAAGGTA[A/G]TGGTGTCTCTGTGAC	80176
rs528076256	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9341780	CGATCTCGTCTCACC[A/G]CAATCTCCACCTCCC	80176
rs528098438	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9300327	CTGAGTCACCCTAAC[A/G]CTTCTAGTTTTGAGT	80176
rs528132427	snp	A/G	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9336597	GGATCCTCTGCCCGC[A/G]TGCGTTCAAGGAAGA	80176
rs528149713	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9341126	CTTGTGTTCTCAAAA[C/T]GTGATAAATGGAATA	80176
rs528168198	snp	C/T	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9309235	GATAAGCTAGATCCC[C/T]CCTCAATTCCTGTGT	80176
rs528244920	snp	C/T	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9314535	AGAGAGGCAGGTTAG[C/T]GAAAGGGAGAGCAAG	80176
rs528290814	snp	C/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9351185	GATTTACATATTGTC[C/T]GGAGAGCCTTAAGTA	80176
rs528306867	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9346197	TGTGTGAGACGGGGC[A/G]GCAGAGGGAGGGAAC	80176
rs528361374	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9307098	ACGCCTGGCTAATTT[G/T]TGTATTTTTAGTAGA	80176
rs528395219	snp	A/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9314042	TTAGCCAGGTGTGGC[A/G]GCGGGCACTTGTTAT	80176
rs528396158	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9305827	CTTTCTCTGTCTAGT[A/G]GGTGAGACAGGCCCG	80176
rs528461729	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9347552	CGCAGAGAGAATCTT[C/T]TTAAATTCTGTTCTT	80176
rs528474177	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9342430	GCCCCAGCGTCAACC[A/G]TGGGAGAGCACGGAG	80176
rs528547933	snp	C/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9302822	GGTGCTGGTTTCTCC[C/T]GTAGCCAGGATTCAC	80176
rs528554818	in-del	-/GTGA	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9294314	TGCGTCTGTGTATGT[-/GTGA]GTGTCTGTGTGTCTC	80176
rs528603813	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9315998	GGCCTCTTGGCAGAC[A/G]GGTTCAGAGGTGGAA	80176
rs528620561	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9352485	TTTATTTATGTCCCG[C/T]CTGTGGCTGCTTTTG	80176
rs528634947	snp	C/T	0.00358779	0.0422022	intron-variant	SPSB1	GRCh38.p7	1:9357499	GTAACCTTGGGGATA[C/T]TAGGGCCTCTCCGGT	80176
rs528694860	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9325332	GGGCTGTGTGGGATT[A/G]AGCTCTTGCCACCTT	80176
rs528698330	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9352013	CCAGCCTCCCTCCTC[C/T]CAGGCCCTCCCTCCC	80176
rs528712639	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9320283	ACTGCAGGGCGGTCA[C/T]CAGCCATTATTGCCT	80176
rs528741441	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9344273	AGTTTCTGATTCAGA[A/G]AGTCTAACGGGATCA	80176
rs528780899	snp	C/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9324982	CCTGTGAGCGGGTCA[C/G]TACTGGGTAGGCAGC	80176
rs528821604	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9301024	GGATGGGGGTGAAGG[A/G]AAATCCTCCCTGGCA	80176
rs528888286	snp	C/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9295719	CCTTCCTGCACCTGC[C/G]CCTCCTCCTGGGTGG	80176
rs528939562	in-del	-/TTA	0.00438332	0.0466095	intron-variant	SPSB1	GRCh38.p7	1:9312740	GGTTTTCTTTGGGTT[-/TTA]TTATTATTATTATTA	80176
rs528949250	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9336642	CAGGGGCAGGAGGCC[A/G]CTGCCTGAGTTCACC	80176
rs528976005	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9301354	AAAAATAAAAAATTA[A/G]CTGGGCGTGGTAGCT	80176
rs529027354	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9367757	ATTCCAACACAGGCT[A/C]CTCTTTCCCCCTTCC	80176
rs529066189	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9336437	CTCCACGTTGGTCAG[G/T]CTGGTCTCAAACTCC	80176
rs529086816	in-del	-/GT	0.0221141	0.102801	intron-variant	SPSB1	GRCh38.p7	1:9293976	TTTATGTGCCTCTGA[-/GT]GTGTGTGTGAGTCTG	80176
rs529142680	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9341817	AAGCGATTCTCCTGC[C/T]TCAGCCTCCTGAGTA	80176
rs529144915	snp	G/T	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9346322	GGTTTTACTGTTCTG[G/T]GGTCAGTCGGACACA	80176
rs529186976	snp	A/T	0.0368353	0.130617	intron-variant	SPSB1	GRCh38.p7	1:9309293	GAGTGTGAGAGAGAG[A/T]GAGAGAGAGTGTGTG	80176
rs529215585	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9321026	GTGGGAGTTGCTGTG[C/T]GGGGGATTCTGGCTG	80176
rs529223350	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9311224	GAATGCCCGCTCTGT[A/C]CTGGCTGTCACAGTG	80176
rs529269343	snp	A/C/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9340283	GCAGAGGAGGGGCCT[A/C/G]GGGGGGAAGGCAGGG	80176
rs529408924	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9316073	GGAGGTGGTGGGTCC[A/G]CAGCGGCACAGTGGT	80176
rs529425226	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9307506	TTGCATGGCCTTCTG[C/T]GTCTGACTTCTGGCT	80176
rs529494131	snp	G/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9353193	GAGCCGCCTCAGCCC[G/T]CCCGGCCCCTCGAGA	80176
rs529501629	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9358502	GGCACCACGTCCACA[A/G]CCAAATTTGCCTCAA	80176
rs529544414	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9320725	CGGGCTCGCCTCTCT[C/T]GGCTCTGGCTGGCCA	80176
rs529580325	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9325437	AAGGTTCCATAGCAG[C/G]TCTGGGACAGAGAGA	80176
rs529583824	snp	A/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9325958	CCAGAAGACCAGTGG[A/G]GCAGGCAGGAGAGAA	80176
rs529593977	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9363841	AAGTAGCTGGGACTA[C/T]AGGCATGCACGACCA	80176
rs529610778	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9308155	TCCAAGACATGTCAG[G/T]CCCAAAGGGGGTGGA	80176
rs529621488	snp	A/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9344661	ATGGTGACATCATGA[A/T]CGCTGCCCTTCTTAT	80176
rs529641735	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9358081	TCTGTCTTGAAGTCT[C/G]CAAGCCTGCAGCTTC	80176
rs529645498	snp	A/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9313856	GGCTGGGGATCTCGA[A/T]TCTCCTGCTTTTCCC	80176
rs529678890	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9348210	TCGGCCTCTCAAAGT[A/G]CTGGGATTACAGGCG	80176
rs529713721	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9346835	CTGGGTATGGGGACG[C/G]ACCAGCTGTTCTCTT	80176
rs529722766	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9349858	TGCTAGGAGTTCCCA[A/G]CCCAGAGTGACTGGT	80176
rs529737713	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9318621	TGTGAGACTTACCTT[G/T]CGGAATCGTGCAGGA	80176
rs529772284	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9312718	TCTCATCAAATTGGC[A/G]TGGTTTTGGTTTTCT	80176
rs529831217	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9346480	AAAGAGGGTGTAGCC[A/G]TTCCTTCAACAGACC	80176
rs529854462	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9355708	CCTTCATCCCACAGT[C/T]CTGCTCACCGGTTGT	80176
rs529870021	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9366854	GCTGGGATTACCAGC[A/G]TGAACCACCATGCCC	80176
rs529874630	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9323223	CACGAAGTGCCCTGG[A/C]TGGGCTGGCGGCTTT	80176
rs529877151	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9292216	CAAAGTCTTTAAAAT[A/C]TTCCCAGTCCCAAGT	80176
rs529905684	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9349508	GGCCTTGGCGCCAGC[A/G]CCGTAGATGCGTGTC	80176
rs529909025	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9327996	GACCTTGGATGGTGA[A/G]TGGAGTGCTGCAATC	80176
rs530043628	snp	A/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9351348	AGATGTGGTGACCAG[A/G]AAGACAGGAGAACAG	80176
rs530166867	snp	C/G	0.00279162	0.0372561	intron-variant	SPSB1	GRCh38.p7	1:9362301	CTCAGAGTTTGGGGG[C/G]GATAGGGGACCAAGG	80176
rs530169435	snp	A/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9329808	GGTGGGGCCGTGGGG[A/G]TGGTAGGCTTGGGTG	80176
rs530178721	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9323870	GGGACCTTGGAACCC[A/G]AGCCTTCTCCCATCC	80176
rs530217505	snp	A/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9335117	TTTTGAGGAATTGCC[A/G]TATTGTTTTCTACAG	80176
rs530231962	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9293575	CCTCCCGCAGCGCCT[A/C]CCCCAGGGAGCCTGC	80176
rs530241313	snp	C/T	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9319391	GTCAGGTGCTTTGCT[C/T]CTCCTCCCTCCTCCC	80176
rs530241351	snp	C/G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9324530	GGGACTCGGTGTGTC[C/G/T]GATGAGGAAACCAGC	80176
rs530252721	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9362006	CGAATTTTCTTTAAC[A/G]GCTCCCAGATGGGTT	80176
rs530253161	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9294458	TGGTTCTGGATAGCC[A/G]GGCATGCTGGGCCAC	80176
rs530275222	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9331278	TGGCCGCACCTCTGT[C/T]ATAAATACCCGTTAT	80176
rs530286455	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9299586	CCGGGTTCAAGCAAT[C/T]CTCCTGCTTCAGCCT	80176
rs530322935	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9299941	TTTACTCCAACCTGG[A/G]CAACAGAGTAAGACC	80176
rs530335033	snp	C/T	0.00279162	0.0372561	intron-variant	SPSB1	GRCh38.p7	1:9307065	CCTGGGTAGCTGGGA[C/T]TACAGGCACGTGCCA	80176
rs530338254	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9367057	CACCAGTGGGGAAGA[A/G]CAGGGATCGCCTGGG	80176
rs530357112	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9313447	AAAATAACTTGCCCA[A/G]GGCTGCACAGCCAAG	80176
rs530371819	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9334678	CCATTCCTGCTCCCC[A/G]GAGCTCCTGGCACTG	80176
rs530403006	snp	A/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9340404	CAGTGATTCACTGTA[A/G]TGCATGTCAAGGCAA	80176
rs530406270	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9304058	ATGGGGTCAGCCACC[A/G]TCCAATCAGCTGGTG	80176
rs530448117	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9304522	TGGCGGTTCATATCC[C/G]TGACCTGCCAGTTGG	80176
rs530449061	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9299352	TTCCACAGATATCAT[A/G]CTGGGGCTGGGCACG	80176
rs530502084	snp	A/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9309174	GGCATGGGGTGTCCT[A/T]GCACTTCCATGCCAT	80176
rs530502112	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9346139	AAATAGCAGATTGCT[C/T]GGGGCATGTTTCTCT	80176
rs530536753	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9304976	CTGCTGCTTGGGTGC[C/T]GTTGCCCCATCCTGG	80176
rs530555183	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9308825	CAGCCTGTGTTTTTT[C/T]CTACTGCGACAGTGG	80176
rs530582724	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9319182	TGAGACTCCATCTCA[A/G]AAAAAACAAAACAAC	80176
rs530704582	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9323276	AGTTCCCGCCGAGCC[A/G]AGGGGGGCTGTGGCT	80176
rs530713774	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9349964	GACACACGCCACACA[C/T]GCAGACACAGGCAGA	80176
rs530813490	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9351890	CGGGTGTGTGGGCCA[C/T]ATTCCCTGGCTAGGC	80176
rs530815578	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9352432	CCCAGGCCAGCCTGT[C/T]CTTATAAATAAAGTT	80176
rs530821934	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9346823	GCTGCCACCTGGCTG[A/G]GTATGGGGACGGACC	80176
rs530891802	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9310505	CCTGACCAGCCTGGG[C/T]AACATGGTGAAACCC	80176
rs531025739	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9324965	CTGGTGGATCGGAGG[C/T]GCCTGTGAGCGGGTC	80176
rs531033325	snp	G/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9356996	GATGGGTGGGTAGGG[G/T]GTGGATGAGTGTTTA	80176
rs531039532	snp	A/G	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9330498	AATAATAATAATAAA[A/G]ATTTGCCAGTCTCCT	80176
rs531040819	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9324561	TTGGGTGGGGAGGGG[G/T]AGTCAAGACAAAAGC	80176
rs531065743	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9335788	ACTCCAGCCTGGACG[A/G]CAGGGCAGGACCCTG	80176
rs531067646	in-del	-/CCCT	0.297128	0.245518	intron-variant	SPSB1	GRCh38.p7	1:9362179	CACCAGGGCCACCCA[-/CCCT]CCCTCCCTCCCTCCC	80176
rs531095469	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9322608	CTGAGAAGTGGCATC[A/G]TTGCGGACAGAGGTG	80176
rs531111284	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9305990	ACATTTGTGCAATTG[C/T]GAGTAACGTGGGAGA	80176
rs531128321	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9364197	TGAGCCACATTCTCC[C/T]GGGAGGGAGCTCAGG	80176
rs531148225	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9362603	TTTTTCCTTGACCTC[A/G]CCGTTCTGCAGCTCG	80176
rs531150501	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9295017	GGCTGTGGACCAAGA[A/C]TCCCCAGTCCTGAAA	80176
rs531161255	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9344005	GTGTTAGCCAGGATG[A/G]TCTCGATCTCCTGAC	80176
rs531172649	in-del	-/TGTG			intron-variant	SPSB1	GRCh38.p7	1:9294249	GTCTTTGTGTCTCTT[-/TGTG]TGTCCACACGTGTCT	80176
rs531209649	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9355065	GAAATCCCGGGGGTC[A/G]GGGGATGAGCCCCCC	80176
rs531230188	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9352503	GTGGCTGCTTTTGTG[C/T]GACAACAGCAGAGAC	80176
rs531281308	snp	A/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9299960	CAGAGTAAGACCCTG[A/T]CTCAAAAAAAAAAAA	80176
rs531295952	snp	C/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9317301	AATAAATGTCACTGG[C/T]GGAAGGTGGCATGTG	80176
rs531307530	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9322208	AATCAGCACTTAAAA[A/G]TGCATCAGGCTGAGT	80176
rs531337895	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9316077	GTGGTGGGTCCGCAG[C/T]GGCACAGTGGTCTCC	80176
rs531384718	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9361439	CGACTTCCACGAGGG[A/G]CAGCTGTTTGTAGGG	80176
rs531424899	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9321600	GATGCATAGGCAGCT[C/T]GCTAATGCTGTGTTT	80176
rs531428954	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9333103	CCTCCCAGGTGCACA[C/T]TCCATGGGAAAATGG	80176
rs531430429	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9344770	TCACGTAGGCTGGGT[A/G]GTGGCCCCTGAAATC	80176
rs531497165	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9306858	CCAAGCAAGATGTCC[C/T]GGACATGCAGATGTG	80176
rs531527818	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9349956	CACACACAGACACAC[A/G]CCACACACGCAGACA	80176
rs531564080	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9299282	GCTGATGGGTATATC[A/G]GCTCTCCAGCCCTAT	80176
rs531567417	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9366074	ATGCAGCTGAATGAA[C/T]TCAGCCTCCTTTGTA	80176
rs531591985	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9336833	CACTAGCCCTCCATC[C/T]CCATTTATAGTTCTT	80176
rs531647540	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9332540	ATATTTGGTGGACAC[A/G]TCAGGTTCACAGGCA	80176
rs531664378	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9301946	TTCGTCTTCCCTGCA[A/C]ACAGTGCTTCTGCCA	80176
rs531715035	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291844	ATGCCCACTCAGGCC[A/C]GCCCAGCCCAGGGCA	80176
rs531795060	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9333899	TTGGCTGGCTCAGAG[A/G]CAGGTGGGGCCTGGC	80176
rs531855900	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9334294	TTTCACCATGTTGGC[C/T]AGGCTGCTCTCGAAC	80176
rs531874774	in-del	-/CCTT	0.0700422	0.173537	intron-variant	SPSB1	GRCh38.p7	1:9362192	CACCCTCCCTCCCTC[-/CCTT]CCTTCCTTCCTTCCT	80176
rs531911922	in-del	-/CCTCGAGAGCCGCCTCAGCCCGCCCGGCC	0.00597247	0.0543191	intron-variant	SPSB1	GRCh38.p7	1:9353172	TCCATGCAGCTCTGA[lengthTooLong]CCTCGAGAGCCGCCT	80176
rs531961383	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9333737	GCACAGTCATTTTTT[C/T]ATTCCAACGGAAAGG	80176
rs531973255	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9344432	CTGTGGGTCTCGTGA[C/T]GGGACCGAGCAACTT	80176
rs531989954	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9349770	AGTTCCCAACCCACC[A/G]TTTTATGGCTGTTTT	80176
rs532031124	snp	A/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9311958	GCTAAGTATTGAGAT[A/T]CAGGAGACCTCATGC	80176
rs532101113	snp	C/G	0.00478085	0.0486577	intron-variant	SPSB1	GRCh38.p7	1:9322826	AGCCCTGACGTGTAG[C/G]GAAGCGCTGCGTTAG	80176
rs532101556	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9312683	ATTTTGCAATGATTG[C/G]ATGATTGTGCATGGA	80176
rs532113058	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9317993	CAGAGGAAGCTGGGT[A/G]GACAGTCGCAGGTTT	80176
rs532143370	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9355076	GGTCGGGGGATGAGC[C/G]CCCCTTGCTGTCTGA	80176
rs532222329	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9360697	CTCTCCGTGGCCCCT[C/G]CTCTTCTTAGAGGGA	80176
rs532296631	snp	A/G	0.0376037	0.131863	intron-variant	SPSB1	GRCh38.p7	1:9365562	ATTCAGTGGCCTCTT[A/G]CGTGGTGAGATGTAG	80176
rs532366014	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291664	GGCTTAAGTGATCTG[C/G]CTGCCTCAGCCACCC	80176
rs532367332	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9322240	GAGTACCAGCATCGT[C/T]TCCTCTAATCCCCAC	80176
rs532518327	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9292499	CGGCGAGGCCTTGCT[A/C]GGGGTTCCTGGGACA	80176
rs532568803	snp	A/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9303893	GATGATTCTCAATGC[A/T]TCAGCACACACTGAG	80176
rs532582557	snp	A/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9323839	TTGCCCACGGACGGC[A/T]GGGGCTGTGCCATGT	80176
rs532583178	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9339962	TCTGATGTGTGTTTC[C/T]TCCAGCCCCCCACCT	80176
rs532605441	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9299309	CTATGTCACAGTTTA[A/G]TTCACAGTCATCTTG	80176
rs532672518	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9323347	CTCAGCAGTGGATGT[A/G]CCCTCCATGGAGTCA	80176
rs532676822	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9294726	TTGGAAGAATTTTCT[C/T]GTTGGGGGGGCTGGG	80176
rs532682019	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9361494	TGTGCCTTCCCGGGG[G/T]TCTCCCAGCCCACTG	80176
rs532683752	snp	G/T	0.0162398	0.0886349	intron-variant	SPSB1	GRCh38.p7	1:9358066	AATACAGATGCTGAC[G/T]CTGTCTTGAAGTCTC	80176
rs532684283	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9299558	AATCTCGGCTCACTG[C/T]AACCTCCGCCTCCCG	80176
rs532701080	snp	C/T	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9313322	GGAAAATCGCTTGGA[C/T]CCGGGAGGCAGAGGC	80176
rs532748796	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9296279	TGCCTCCATGTCCAT[C/T]CTGCTGAGGATTGCA	80176
rs532840771	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9368355	CGTGCCCAGGCACAA[A/G]TATGTCTCTGGGTCC	80176
rs532849752	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9313274	ACGTGGTGCCGGGCA[C/T]CTATAATCCCAGCTA	80176
rs532874518	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9303083	CAGGCTGAGAGGGGA[A/G]TGATGGTGTTGGCTG	80176
rs532892802	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9363980	GCTGGGATTACAGGC[A/C]TAAGCCACCGCGTCC	80176
rs532904283	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9325594	CAGGCATGTATTGAG[C/G]ACTTACTCTGTGCCA	80176
rs532907455	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9295832	TGTATCAATTTTTCT[C/T]GAGAAATAGGTTGTA	80176
rs532957478	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9358697	GCCAGACCTGCTCTT[A/G]TTGCCTGCCCACTGA	80176
rs533012861	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9337616	CTCCAGCCTTGCTGA[A/G]GTGGGGTCCCCAGTT	80176
rs533050649	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9341929	CTGGTCTCGAACTCC[C/T]GACCTCAGGTGATCT	80176
rs533076842	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9338131	CTCCCTGCAGGTCCC[C/T]TGTCCCCTCGCTCCT	80176
rs533083407	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9303468	TTTCCTCCCTATTTT[G/T]TTCAGAATACGGTTG	80176
rs533087676	in-del	-/AATAA			intron-variant	SPSB1	GRCh38.p7	1:9313434	AATAAAATAAAATAA[-/AATAA]CTTGCCCAGGGCTGC	80176
rs533125972	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9307171	GACCTCAGGTGATCT[A/G]CCCGCTTTGGCCTCC	80176
rs533175454	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9365728	TGAATATTAAAGAAC[C/T]TTAATCCACTTTTTA	80176
rs533201232	snp	A/C/T	0.00199529	0.0315338	intron-variant	SPSB1	GRCh38.p7	1:9332658	AGCAGGAAGAACAGG[A/C/T]GGAGGAGCTGAGACA	80176
rs533217405	snp	C/T	0.00517822	0.0506191	intron-variant	SPSB1	GRCh38.p7	1:9338820	TCCTGGGGGCGCTCC[C/T]GCCTTGCTCTGCTGT	80176
rs533218400	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9347458	CGTTTTTTCCCTCCC[A/G]CCCACAATCATTAAC	80176
rs533301504	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9310266	CTCTTGGGTTGATCC[A/C]AGGAAGCTTCAAGCA	80176
rs533309088	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9316791	GGGCCGCAGCAGCTT[C/T]GAGCCCAGCTTGGGA	80176
rs533309177	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9310956	GTTCTTCTAAAAACA[C/T]TTCGCCATCTTTGGA	80176
rs533327667	snp	A/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9302013	ACTGTCACGCTGTCC[A/G]TGTAGCACTGCTTCC	80176
rs533377094	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9297342	GACTGCTGAGTAGGA[A/G]TATAGGATTCCAGGG	80176
rs533498974	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9306985	CAGGCTAGGGTGCAG[C/T]GGCACAGTCTCAGCT	80176
rs533502650	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9321118	CTTCTACCCCTCCCC[C/T]GAAAAGAAAACAACA	80176
rs533534635	in-del	-/C	0.00953873	0.0683987	intron-variant	SPSB1	GRCh38.p7	1:9333528	AGAGACGGGGTTTCG[-/C]CCATGTTGGGCAGGC	80176
rs533562770	snp	C/T	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9348030	GCTCACTGCAACCTC[C/T]GCCTCCTGGGTTCAA	80176
rs533564764	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9353893	ATTGCACTCCAGCCT[A/G]GGCAACAAGAGCAAA	80176
rs533578748	snp	C/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9348578	CAGGCTTCCTTCCCT[C/G]TGTATCTGCAGACCT	80176
rs533601533	in-del	-/CAAGGC	0.102014	0.201495	intron-variant	SPSB1	GRCh38.p7	1:9340416	TAGTGCATGTCAAGG[-/CAAGGC]CAAGGCGTTGTGTTA	80176
rs533704488	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9353281	GGAAGAGGGGAATTC[A/G]GGGAAGGCCACACCC	80176
rs533734877	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9331231	AGTGACCTTTGTCAA[C/T]GACTGTGCACTCGAT	80176
rs533774356	snp	C/T	0.00795532	0.062565	intron-variant	SPSB1	GRCh38.p7	1:9342561	CTAGGAATCCAAACG[C/T]CCCTCTCCCGCCTCA	80176
rs533796248	in-del	-/T	0.00279162	0.0372561	intron-variant	SPSB1	GRCh38.p7	1:9314169	AACAGATTGAGACTC[-/T]TATCTCAAAAAAAAA	80176
rs533833339	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9320795	TTTCTTGTTTCCTCG[G/T]GGGGGATTTTAAATT	80176
rs533880340	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9362925	AAGCTTCCTGGGGAT[A/G]GGCATAGCAGCCAGA	80176
rs533918343	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9326763	AGAAATGGTAAGCCC[A/G]CTGCTTCTGAGGGGC	80176
rs533919182	snp	C/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9352766	CAACCTCCCTGTTAT[C/G]GTCCCTCCTGGCATT	80176
rs533946763	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9365960	GGGGTCTGCTCTGGC[A/G]AAGCGGGCGAGCAGG	80176
rs533962383	snp	C/T	0.00478085	0.0486577	intron-variant	SPSB1	GRCh38.p7	1:9325198	CTGTACTCCGCCCTC[C/T]GGCCTGAGCCAATGC	80176
rs533963165	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9327753	TAGGCTTTGTAGACC[A/G]TATGGTGTCTGCCGC	80176
rs534011464	snp	A/G	0.00438332	0.0466095	intron-variant	SPSB1	GRCh38.p7	1:9340160	GTGACCAGTTCCCTC[A/G]CCCCTGTAGGAACTG	80176
rs534018811	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	SPSB1	GRCh38.p7	1:9369901	GCAGAGTGTGAGCCA[C/T]TGTGGGCGTCCTCAG	80176
rs534021689	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9302084	TCATGTGCAGGGAAT[G/T]GGCCGGTGAGCACGA	80176
rs534027491	snp	C/T	0.00874735	0.0655527	intron-variant	SPSB1	GRCh38.p7	1:9325663	CTGAGTTCCAGCCCC[C/T]GTGTTCTCACAGGGG	80176
rs534027911	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9320483	AGGGCTGGGAGAAGC[C/T]GTTTCCCTTGGCGTT	80176
rs534076968	snp	C/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9301790	CTAGTCTGCCAGAAG[C/T]GGAGACTAACACTGA	80176
rs534120716	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9295515	TGGAGCTGGGTGAGG[C/G]CGTTTCTTGGGCTGC	80176
rs534197037	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9306311	TCCACCACGGAGAGC[A/G]TTTGGAGCACAGCAG	80176
rs534214946	snp	C/T	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9354196	AGGTCCCTGGATTTC[C/T]GTGTGTCTGGGAGCC	80176
rs534235214	snp	A/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9306567	TAGGTACTACCCATT[A/T]TACAGATGAGAAAAA	80176
rs534249954	in-del	-/CT	0.00358779	0.0422022	intron-variant	SPSB1	GRCh38.p7	1:9327668	GGAGAAATTTGACCC[-/CT]GTTTCTTCACCATTT	80176
rs534364720	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9324188	TGGTTTTTCTCATCC[A/G]GCAAGTGGACACCTC	80176
rs534376800	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9369217	ACGGTTTTTTTTTTC[A/G]GGGCAGGGGACCTTA	80176
rs534388116	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9328888	CCCCCACCCACCAGA[C/T]GCCACCCCAACTTGT	80176
rs534460156	snp	A/G	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9342862	AGCAATTCTGCTCTC[A/G]AAGGCTCTTCACTCC	80176
rs534471753	snp	A/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9304212	GACTCATACCATTGG[A/T]CCCCGGGGTCTTTGG	80176
rs534512878	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9340200	GAGGAGACAGACTCT[C/G]CTTGGGCAGGCTTTC	80176
rs534556809	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9362092	TCAGAGCCTCCTCCC[C/G]GGTGCCTCCTTCCTG	80176
rs534585646	snp	A/C	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9313461	AGGGCTGCACAGCCA[A/C]GAACTCAAGCTGGAC	80176
rs534637005	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9342861	CAGCAATTCTGCTCT[C/T]GAAGGCTCTTCACTC	80176
rs534690261	snp	C/T	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9335330	AACATGGCGAAACCC[C/T]GTCTCTACTAAAAAT	80176
rs534693528	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9342090	AAGCTCATTCTAACC[C/T]GTCTTAGGGGCTTAG	80176
rs534735241	snp	C/G	0.000798403	0.0199641	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9292871	TTTTTCACTTTAAAG[C/G]CGTCGGTTGCTTTTT	80176
rs534755312	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9366763	ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT	80176
rs534769003	in-del	-/AC	0.00835141	0.0640778	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9367835	CCTCTTTGAAAAAAG[-/AC]ACAGAGAATAAACTC	80176
rs534822476	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9340519	TATGGGAACGGAAAC[C/T]TGGGACCATGTTAGA	80176
rs534825266	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9346895	GCCGCCCCATTTTTA[C/T]GGGGCTAATTAAAAT	80176
rs534908352	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9346538	TAATTTTTAGAGGAA[A/G]CAAGGCTCGGGAACA	80176
rs534943568	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9324654	CAGCCTGTCTTGTTC[C/G]TATAAAGGGCACTTT	80176
rs534948532	snp	A/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9344988	CCCTGAAAGCCTGGG[A/T]TTGGTCGGATCCCCT	80176
rs534972913	snp	A/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9305732	GGCCACTTGTCATTC[A/G]TGCTTTTATTCAAAC	80176
rs535009399	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9314212	AAAAAAACAGTGAAC[A/G]GGACAGCTGGAAAAT	80176
rs535015734	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9350999	CACCTGTGAATGTTA[C/T]TTGGTACCTGTGGGT	80176
rs535028670	snp	A/G	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9336781	GCTGCCTTTTCATTC[A/G]GTGATGAAACTGCAC	80176
rs535107023	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9319825	CCTCACATCCACACC[C/T]GCTGTTTCTGTGGCC	80176
rs535140244	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9305308	CAGGGATGTCCCCTT[C/T]AGCAGGTAGCCCTGC	80176
rs535177983	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9351449	TCTCTGGAACACTGT[C/T]TCCACTGAGTTTTAG	80176
rs535225830	snp	A/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9305067	CATTGCCTTCCCTAC[A/T]GGGGCCTCTCCCACT	80176
rs535263137	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9314884	GAGGCTCCAGGGCAG[A/G]GAGAGGACTGCGGCA	80176
rs535269100	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9335404	TTACTCAGGAGGCTT[A/G]GACAGGAGAATCACT	80176
rs535317195	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9362380	GGACAAAGGCTCCAC[A/G]TTGTGTTTGGCTGTG	80176
rs535328181	snp	G/T	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9329475	GGGAAGATGGGCATG[G/T]CCACCCATCAGAAGT	80176
rs535341793	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9304228	CCCCGGGGTCTTTGG[C/T]CCGGGGCTGAGAATG	80176
rs535392112	snp	A/G	0.00557542	0.0525036	intron-variant	SPSB1	GRCh38.p7	1:9357189	TGGATGGATGAGTGG[A/G]TGGATGGATGGGTGG	80176
rs535424013	snp	C/T	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9304445	GAGAATCCTGGCTAA[C/T]GCAGTTATGGTCGCC	80176
rs535437744	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9337475	GCCTCCATGGTTTGG[A/G]GACAGGAAGCCCTCT	80176
rs535458286	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9357715	GGGAGTGGCCTTTCT[C/G]AGACTGTGAATGCAG	80176
rs535484434	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9330112	CAAAGATCAGTGGCG[C/T]AAATAATTGCTAGGT	80176
rs535530381	snp	A/G	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9362169	TGATACACCGCCACC[A/G]GGGCCACCCACCCTC	80176
rs535578989	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9368048	CCCAGGGTGCCCAGC[A/G]GGGCCATGCCATGGC	80176
rs535594415	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9362418	GTAAGAACTGCGTAG[C/T]GTAGAGGAAAACACA	80176
rs535611144	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9306228	CCTTTCGGGTGTGCC[A/G]AGGGATGGCCGAGCT	80176
rs535652845	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9342215	CTGGCCAGGAGAGGA[C/T]CCGTGGGCAGTGGCA	80176
rs535686264	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9336073	CTTCTCTGAGGCTCT[C/T]TGCAGGCTTCCAGGG	80176
rs535716093	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9340633	GCTGGGGAGGGTCCC[C/T]GCAGCACCTGGGTCT	80176
rs535760024	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9314959	TGAGGGAGTGGAGTC[C/G]TTGGCACTGTAGTAT	80176
rs535788117	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9331811	ATCTGGAGGGTGCAA[C/T]GTGCGATCTCATTAC	80176
rs535797792	snp	C/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9346608	GGGTTGTGGCTTTAA[C/T]TGAAACACCATCGGG	80176
rs535881936	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9331335	TGTTTTTTTTTTTTT[G/T]TTTTTTTTTTTTGAG	80176
rs535908145	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9334023	CTCAGGTTTCTGTTT[A/G]TTTTTATATAAACCA	80176
rs535910720	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9339203	GGTGAGGACCTGTGG[A/G]GCTTTTCTCCTGGGT	80176
rs535942513	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9305859	CTCTGCTGATGATAG[C/T]GCTCAGGGTATCAGA	80176
rs536044367	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9343923	CCCAAGTAGCTGGGA[A/C]TAGAGGCGCCTGCCA	80176
rs536063191	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9344826	CTCAGATCCCTTCCC[C/T]GGTCCTTTCCTGGTC	80176
rs536096117	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9312218	TGTCACCCAGGCTGC[A/G]GTGCTATGTTGCTCA	80176
rs536103915	snp	A/G	0.00358779	0.0422022	intron-variant	SPSB1	GRCh38.p7	1:9322318	AACTGAGGTTCGGAA[A/G]GTCTCTCAGGTTATA	80176
rs536175225	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9352220	AGAGGTTGTGGAGCC[A/G]ACCTGGACAGACAGA	80176
rs536183679	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9354709	TCGTAGCTGAGGCAG[A/G]AGAATCACCTGAACC	80176
rs536205316	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9303275	AGGACTGTGAATGAC[G/T]CAGACCCTTCAGGAA	80176
rs536210641	in-del	-/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9311334	TTTCTTTCTTCCCCC[-/T]GATGGGTCTCGGCGT	80176
rs536222199	snp	A/T	0.00953873	0.0683987	intron-variant	SPSB1	GRCh38.p7	1:9333534	CGGGGTTTCGCCATG[A/T]TGGGCAGGCTGGTCT	80176
rs536327790	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9307364	CCATCTTCATCCCGC[C/T]GGAAGGAAACCCCAT	80176
rs536368403	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9302699	AAAGAAGGGCAGTAG[A/G]GTCTTTTGAAGTTGC	80176
rs536373752	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9350087	CACACAGATACATAC[A/C]CGCCTCACATATCTA	80176
rs536407490	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9361583	TTCTACACTGGGGCC[A/G]TGGCCGGGCGGAAGT	80176
rs536533478	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9365965	CTGCTCTGGCGAAGC[A/G]GGCGAGCAGGGCCGC	80176
rs536547125	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9311580	TCAGACTTGAACCAA[C/T]GCTTGAGCCAGAGCA	80176
rs536596118	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9361022	CCAAGTCCCCCGTCC[A/C]GGGAGAGTTGGCTTT	80176
rs536641990	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9350802	CCTGATGCTTCTGTG[C/G]CACTGCTGGGCCCCA	80176
rs536655567	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9345764	ACTAGAGCTCTGGAC[A/C]GTGTGGGATTTTCTC	80176
rs536687560	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9314057	GGCGGGCACTTGTTA[C/T]CCCAGCTACCTGGGA	80176
rs536732690	snp	C/G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9318748	CACTCAGATCAGGGC[C/G/T]TCTGTCAGGCTCTGG	80176
rs536823377	snp	G/T	0.00279162	0.0372561	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9292672	GGCGGCGGCTCGGGA[G/T]AGGGCTGCGGACTAA	80176
rs536861443	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9342218	GCCAGGAGAGGATCC[A/G]TGGGCAGTGGCAGCA	80176
rs536864066	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9323579	TCAATGTTTAGCCTT[C/T]GTGGAATCCAGATGT	80176
rs536958703	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9323093	GCCCCTCCCCAGCTC[C/T]GGCCTTCGAGGACTT	80176
rs536971820	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9312810	GCAGTTTTGGAAGGC[C/G]CCCAGGGAAGGCTAC	80176
rs536979567	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9301828	TATGGCCCCATTCCC[C/T]GGGATGATCACTGCA	80176
rs537002340	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9304754	GGACGTGTCCAGATG[A/G]CAACTGGGCTCAACG	80176
rs537018452	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9299376	GGGCACGGTGGCTCA[C/T]TCCTGTAATCCTAGC	80176
rs537048209	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9340703	CCTGCCACCGAGGGG[C/T]GTGGGATGCACCCGT	80176
rs537051402	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9292732	CGGGCTGACGCGCCC[C/T]GCGCCCCGCGCCCCG	80176
rs537065383	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9339056	TGGTAACCAAGGGCC[A/G]CTTCCCCTTGGAGAC	80176
rs537113321	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9340155	GCAGGGTGACCAGTT[C/T]CCTCGCCCCTGTAGG	80176
rs537148253	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9308167	CAGGCCCAAAGGGGG[C/T]GGACTGCCTCTCATT	80176
rs537170419	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9309094	GCCATGAGGAGGACC[A/G]GGAGAAGGCTGCAGA	80176
rs537187191	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9304105	AAGCTGGAAGAAGGG[C/T]GAATCCTGGCTCTCT	80176
rs537217164	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9306169	CACAGGGCAGGGACT[A/G]AGGGCACCTCAGGCG	80176
rs537261861	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9360875	TGTGGAGGCAGCCAG[C/T]GTAGACCATCTCCAT	80176
rs537272052	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9350960	ATGTCTGTCTTGGTC[C/T]AGTGTTAACAGGAGC	80176
rs537300712	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9329237	GTTGAGGGTTTGTGG[A/G]TGGGGGGAAATGCAG	80176
rs537302296	snp	C/G	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9323663	CTTGCACACATGGCT[C/G]CCCGCGCGTCTCCAG	80176
rs537321150	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9361618	GTACTGAGTTCTCGA[C/T]GTTTCCCTGTGCGGC	80176
rs537338666	in-del	-/AGTC	0.00358779	0.0422022	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9369492	ATGATGGTTGATAAT[-/AGTC]AGTAACCTAATAAAG	80176
rs537404104	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9311405	TTATAATGGAAAATT[G/T]CAAACACAGGGCAGA	80176
rs537420341	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9367106	CTCCTGCCAGCAGGG[C/T]GACCCCTGGCAAGTC	80176
rs537430421	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9348732	CCTTAAATGGCTGTT[C/T]GAAGCTGGCCGAGGG	80176
rs537451321	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9346471	ACATCCCCAAAAGAG[G/T]GTGTAGCCGTTCCTT	80176
rs537526019	snp	A/C	0.00279162	0.0372561	intron-variant	SPSB1	GRCh38.p7	1:9314157	CTCCAGCCTGGGCAA[A/C]AGATTGAGACTCTAT	80176
rs537538146	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9364257	GCCAGATGCAGGCGC[A/G]CTCCCAAGCAGAGAA	80176
rs537554989	snp	A/C	0.0197687	0.0974348	intron-variant	SPSB1	GRCh38.p7	1:9337421	GCCAGCCACCTGCCC[A/C]CCTAGCCAGTGAGAT	80176
rs537575913	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9354064	CCTGGAGACCTGGCC[A/G]CCCCGGGAACAGGGT	80176
rs537600544	snp	C/T	0.0166325	0.0896639	intron-variant	SPSB1	GRCh38.p7	1:9352953	GCTGCCACAGTTGAG[C/T]GGCAGGGGGGCTGTG	80176
rs537652460	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9312244	GCTCAGGTTGGTCTC[A/G]AACCCGTCCTGGGCT	80176
rs537663761	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9294679	GTGTTCATGGTAAAA[C/G]CGCCATCCCTGGTGA	80176
rs537681651	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9319428	TTCCTCCCTCCTCTT[C/T]CTCCTTCTCCTCCCT	80176
rs537734625	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9368913	ACCCCTCCACGTAGC[A/G]TACCCCAGCACCTGC	80176
rs537746906	snp	A/G	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9340938	GGAGAAGACTGGTCT[A/G]GCTCAAAAGGCCAGT	80176
rs537782339	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9322861	CCAGGCACCTCCAGC[A/C]CGCACCCACCCCACC	80176
rs537837569	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9342993	CACCCCCATCCACAC[C/T]CACCCCCTGTCCATG	80176
rs537908162	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9327338	ACGTATGCATGGATA[C/T]GTATGTCTTTGGCAG	80176
rs537925064	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9316581	TGATCGAAGCGGGTT[C/T]AGGGGCTGCCATTTA	80176
rs537928793	snp	A/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9365137	GCTGGGATTACAGGC[A/G]TGAGCCACCACACCT	80176
rs537942001	in-del	-/CCT	0.00597247	0.0543191	intron-variant	SPSB1	GRCh38.p7	1:9330648	CTCTTCCTTTCCTCC[-/CCT]CCTTTTTCTCTCCCT	80176
rs537968268	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9311083	CTTCTCCCGCCTCTA[A/G]CCTCCCAGGCTCCCT	80176
rs537971005	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9322387	TCAGCTCCAAAGTCC[A/G]TGCCTCGCTCTCATT	80176
rs538019299	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9297461	CACACCCTTTCCAAG[A/G]TCAGAGTGAGGAGCT	80176
rs538019346	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9312202	AGGCAGAATCTCGCT[C/G]TGTCACCCAGGCTGC	80176
rs538031398	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9351207	CCTTAAGTAGTTACT[A/G]TCTGGCCCCTGATGG	80176
rs538057972	snp	A/G	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9298108	AAAGCTGCCGTCAGA[A/G]TAGTCTGACTTGTGT	80176
rs538095697	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9325708	GATAACCAAGTGAAC[A/G]TCATTGTGAAGTTCC	80176
rs538128905	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9295941	GCCTCAGTCTGCCCA[A/G]GGGTGTGTTATCCTC	80176
rs538153307	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9320856	TCCTGCGCCGGGTTT[A/G]GCAGGATGGAGTTAG	80176
rs538153977	snp	G/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9307046	GATTCTCCCTCCTTA[G/T]CCTCCTGGGTAGCTG	80176
rs538190163	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9360884	AGCCAGTGTAGACCA[C/T]CTCCATGAGGCCTTC	80176
rs538205391	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9354896	GAGTCCCTGTTCTCC[C/T]TCCTGAAGGACCCAG	80176
rs538243836	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9317666	ATTTTGTATTTTTTG[C/T]AGAGTTGGGGTTTCA	80176
rs538262211	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9349266	GTTTTTCGCTCCTCT[A/C]TGCTTCCCCGAGCCC	80176
rs538263909	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9322882	CCACCCCACCCGCCC[A/G]GACGCTCTTCTCAGC	80176
rs538266589	snp	A/G	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9322985	GGTCACTCCCTTCCC[A/G]TGCCGCCAGCACTGA	80176
rs538267032	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9355160	TTTCGTGCCAAGCGC[A/G]CACAGACCCCTGAGT	80176
rs538290142	snp	A/G	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9309127	TGTGTAGCAGGGAGG[A/G]CATCAAATGCCAGGC	80176
rs538302071	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9343116	CATTCACCTTTTTAA[A/G]AGTACAATTCGATGG	80176
rs538353111	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9293896	TGAATATGTGCCTGC[A/G]TATGAGTGTGTCTGT	80176
rs538463845	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9341342	TGCAGGTAGAACCTC[C/T]GCCAGCAGCCCCTTC	80176
rs538467617	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9348806	CCACCGAGAAATCCA[A/G]TAGGGTCACGCGGCT	80176
rs538483074	snp	A/T	0.0333695	0.124785	intron-variant	SPSB1	GRCh38.p7	1:9333348	TTTTTTTTTTTTTTT[A/T]AAGGCAGAGTCTCAC	80176
rs538503757	snp	A/G	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9338553	CGCCCAGGAGGAAGT[A/G]TACTTTCTTCTTTGC	80176
rs538504052	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9326742	CTTCCCTCCCACTGG[C/T]GGAGCAGAAATGGTA	80176
rs538533742	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	SPSB1	GRCh38.p7	1:9369982	CTGGGGCTGAGTGCA[C/T]GGTGATGTTTGCTGA	80176
rs538536323	snp	C/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9364674	ATCCTAAGCTGGCCA[C/G]GAAAGGCCCCCTTTC	80176
rs538582307	snp	A/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9302188	GTTTAAGAAGATGCC[A/T]GTGGGTGCCTATGGG	80176
rs538596078	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9307327	CAATGTCGTGCAACT[A/G]TCCCCTCTGTCTAGT	80176
rs538600344	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9325802	GAAAGGCCTCAGTGA[C/T]GTGGTGACCTCAGAG	80176
rs538622909	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9338652	GTCTGGGAAGGGAAT[C/T]GTGCTGGCTTCACCT	80176
rs538717909	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9323078	ACGGGCCAGGCGGCC[A/G]CCCCTCCCCAGCTCC	80176
rs538757578	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9312069	GCTCACTGCACCTCA[A/G]ACTCCTCAAGTGATC	80176
rs538758900	snp	A/C	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9343508	TTTATCCATGCATCC[A/C]TTGATGGACATTTGG	80176
rs538816356	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9365827	AGTCAAGGGGAGACC[A/G]TGGATGAAGCCTCAG	80176
rs538858503	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291979	TCAATTGGGTTCCAA[A/G]CTCTGGACAGCTGGC	80176
rs538904165	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9359012	TTGGAAAATCCTGAA[G/T]ATGTTGGGTGAGTGG	80176
rs538930008	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9316621	GGGAGCGTTTTGCTA[C/T]CTTAGAGCCCACCCG	80176
rs538981491	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime	SPSB1	GRCh38.p7	1:9355812	ATTCTGTCTGGCCCC[A/G]ATCAGAATACTGGAG	80176
rs538987590	snp	C/T	0.00318978	0.0398085	intron-variant	SPSB1	GRCh38.p7	1:9344067	TGCTGGGATTACAGG[C/T]GTGAGCCACCGCACC	80176
rs538998112	snp	C/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9298173	CCTAGAAGTGAAATA[C/G]ACAGGAAACCCGTGA	80176
rs539024569	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9358132	CTCCTCCTGCTCCTC[C/T]TCCCCCACGTCAGCC	80176
rs539057737	snp	A/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9350030	ATATATACACACATG[A/T]AGACACACCACACAC	80176
rs539092086	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9320791	CGTGTTTCTTGTTTC[C/T]TCGTGGGGGATTTTA	80176
rs539192093	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9360438	ACAGGGTATTCGTCT[C/T]CTGGAGCTGCTGAAC	80176
rs539194322	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9298880	GGTGAGGGCTGTTAT[G/T]GTGGGAAAGGCCAAG	80176
rs539224500	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9362454	ATCCTATGATGGCCA[C/T]CCGACCCGTGACATT	80176
rs539231236	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9300388	CAGGTTGCTGTGCAA[A/C]CTGCTTTGCCACTTG	80176
rs539255347	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9295297	ATCACTTTACAAGTC[C/T]TCCTTTTCCAGTCTG	80176
rs539266430	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9322534	ATGGTTAATTGAGGA[A/G]GGATGGCAATCATGA	80176
rs539284126	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9328167	ATAGAGCCAGACGAA[C/T]GTGGCTGTGTGGAGG	80176
rs539299627	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9324821	CAACACTGGGCCAGA[C/T]AGTCGTGTTTGCGAC	80176
rs539352354	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9367381	GATAATATTGCTGCT[A/G]TGGTTAGCGCTGTTT	80176
rs539418535	in-del	-/C			intron-variant	SPSB1	GRCh38.p7	1:9333328	TCTTCTTGTCAGCTT[-/C]TTTTTTTTTTTTTTT	80176
rs539431961	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9332063	TCAAAATTTAAAAAA[A/G]CCTTGGCCAGACGAG	80176
rs539461335	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9352674	TCCCCCTCCTTCCCC[A/G]TCCCTCCCTGTCTCA	80176
rs539474096	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9325082	TGCACTCGCTGGAAG[C/T]TGGGACTCCAGAGCT	80176
rs539491519	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9326268	TTATTCCCAGCACCA[C/T]CCCAAGGGCTGGGCA	80176
rs539498182	snp	G/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9362884	GCACTCTCATTCACA[G/T]AAATTATTTAAATGA	80176
rs539519344	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9337904	TTAGGGGCGGGAGGG[G/T]TAACTTAAGAGAGTG	80176
rs539544941	snp	A/C	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9306543	ATAATGTCCGTGATA[A/C]CTATAGGGTAGGTAC	80176
rs539580685	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9301725	GCATGGGCTCAGCAG[C/T]ATGGACTGCCACTCA	80176
rs539686866	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9330738	GGTAAAACATACAAA[A/C]ACCTAAAATTTACCA	80176
rs539715684	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9336319	TGCAACCTCTGCCTC[C/T]GAGTTCAAGTGATTC	80176
rs539726467	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9316168	CTGGCAGGGGGTGGG[C/G]ACCTGGGTGAAGAGG	80176
rs539763132	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9310450	GTAATCCCAGCACTT[C/T]GGGAGGCCGAGGCAG	80176
rs539770400	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9331447	GCGATTCTCCTGCCT[C/G]TGCCTCCTGGGTAGC	80176
rs539904491	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9309627	ACGGGTGGATCACCC[A/G]AGGTCAGGAGTTTGA	80176
rs539933388	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9368550	CCTTGCACAGGGTTG[C/T]ATTTCTTTAGTCTTC	80176
rs539945213	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9369182	GGGTGAGAAATGTAC[A/G]TTACCCCCTTATTAT	80176
rs539975032	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9296043	GCTCTCCCCTCCCCC[A/C]GTTATCTGATAACAT	80176
rs539981995	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9309580	AGGCACAGTGGCTCA[C/T]GCCTGTAATCTCAGC	80176
rs539982602	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9306260	TGGGCCTTCCTAGCC[A/G]CGTCCTGCAGCAGTC	80176
rs540021920	snp	A/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9342531	TGTTGACCTGCTCAG[A/T]GAGAAAGTAGGCGCC	80176
rs540071205	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9352316	CCAGCCTCTGGGGAT[A/C]CCCCGCTCCCCACCA	80176
rs540136171	in-del	-/TTTTAATT	0.030278	0.119257	intron-variant	SPSB1	GRCh38.p7	1:9312156	CTAATTTTTATTTTA[-/TTTTAATT]TTTTAATTTTTTAAT	80176
rs540143528	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9294821	CTCTCCCTTCTGCCC[C/T]GTCCCCCTCCTCAGA	80176
rs540172577	in-del	-/C	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9297952	AGCTCCGTGATCCAG[-/C]CCTTACAGTGGGAGC	80176
rs540217189	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9353824	TTGAGAGGCATAGGC[A/G]GGAGAATCGCTTGAA	80176
rs540219170	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9321373	CAGGGGGTGGGCTCC[A/G]AGCTCCAGGGCCCAT	80176
rs540224753	snp	A/C	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9336978	CAGTGCTGGGGCCTG[A/C]CTCCCTATCGTGGCA	80176
rs540225895	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9342325	GAGAAGAGGTTTGCG[C/T]AGTGACAAGTCCAGA	80176
rs540280375	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9320971	CCCTGCTTAAAATCT[C/T]CTTCCCGAGTCCCTG	80176
rs540359460	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9341795	GCAATCTCCACCTCC[C/T]GGGTTCAAGCGATTC	80176
rs540365289	in-del	-/CCCCGCGC	0.000399281	0.0141238	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9292743	GCCCCGCGCCCCGCG[-/CCCCGCGC]CCCCGGCCTTCCCTG	80176
rs540377197	snp	A/G	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9351658	AGGGTGGATCTGTGC[A/G]GCCACATTTTAAAAT	80176
rs540447370	snp	A/G	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9315114	ATCTCCCCTCTCTGT[A/G]GAGGTGAGGAGGGCA	80176
rs540464498	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9325935	AGCTTGGCAGGTACC[A/G]GGAACAGCCAGAAGA	80176
rs540467112	snp	A/C			utr-variant-3-prime	SPSB1	GRCh38.p7	1:9368812	CTCTGGACCCAGGGT[A/C]ACAGCCCCAGTTCAT	80176
rs540537655	snp	C/T	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9320435	CAGATATGGGGTGGC[C/T]CCATCTCCGCCATTT	80176
rs540561558	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9357272	ATGAGTGGGTAGATG[C/G]ATGGATGGATGGATG	80176
rs540581077	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9349778	ACCCACCGTTTTATG[C/G]CTGTTTTTCTCTCTT	80176
rs540599362	in-del	-/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9322069	ATATGTGCACTCCCC[-/G]AGCACCCATCCTGCA	80176
rs540604982	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9296368	CTTGGCACCCAAGCC[C/T]TTCACCAGTAAGTTT	80176
rs540612362	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9345946	ACAAGCCCTGCTGGT[A/G]GTGGCCCCTTTGCCA	80176
rs540654979	snp	C/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9318511	GTTTCCAGCATCCAA[C/G]GAAGACCCTGAGTTT	80176
rs540697647	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9313288	ACCTATAATCCCAGC[C/T]ACTTGGGAGGCTGAG	80176
rs540708477	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9358465	AGTTCTGTGTCTGTC[C/T]CCCTAGGTGTCAGAA	80176
rs540751913	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9361242	CTGGGCTCCTAAGTG[C/G]TCCTCCTGCCTCGGT	80176
rs540775593	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9312996	CTGAGTGCTTGCTCT[A/G]TGCCTGGCACTGTTC	80176
rs540799409	snp	C/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9350229	AGGAAGCACCAGACA[C/T]TGGACCCCTGCGTGT	80176
rs540811231	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9355614	GGCTCCAGCCTGCCC[A/G]TGTCAGGCATGACAG	80176
rs540843992	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9356780	AGCTAGATTACCTAA[C/T]GGTGCCTCATGAATG	80176
rs540882588	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9337890	ACCCAAGAGCACCTT[C/T]AGGGGCGGGAGGGGT	80176
rs540924800	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9368272	TGGCTGTTCTGTTAC[C/T]TTCCTTCCACCTGTG	80176
rs541002087	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9305416	GTGACCTGTGGGCTC[C/T]AGGAGGGCAGGACCC	80176
rs541052165	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9322235	GAGTAGAGTACCAGC[A/G]TCGTCTCCTCTAATC	80176
rs541116897	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9292160	ATGGACACTACACAG[C/T]GAGGGGTGGGGAATG	80176
rs541134863	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9367001	CCATGTGTTCCGACC[A/G]ACAGGCCCCAATGGC	80176
rs541166147	snp	C/T	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9361682	CCCGTGCTCTGATTC[C/T]TCCTCAAGGCTCGAG	80176
rs541174729	snp	A/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9299109	ATTATTGTAAACTTA[A/G]CCAAGTGGTGACTGC	80176
rs541178273	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291690	CACCCAAAGTGTGGG[A/G]ATTAAGGGCGTGAGA	80176
rs541198667	snp	A/G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9366033	GTTTCAGACTCCTGA[A/G/T]ATCTGAAGCTGACGG	80176
rs541336799	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9303560	TAGAACATGTGTTGA[A/G]TCTATAGCAGTATTT	80176
rs541342556	snp	A/G	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9365564	TCAGTGGCCTCTTGC[A/G]TGGTGAGATGTAGGA	80176
rs541355238	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9345254	GGAGGGCAAAGAGCA[A/C]CAGCGTCTCTGAGCC	80176
rs541366282	snp	A/G	0.00557542	0.0525036	intron-variant	SPSB1	GRCh38.p7	1:9294334	TGTCTGTGTGTCTCC[A/G]AGTGTGTGTCTGTGT	80176
rs541414345	snp	A/G	0	0	intron-variant	SPSB1	GRCh38.p7	1:9363628	ATGGCTGGGGCTGGG[A/G]CTGCGGTGTCAGCCA	80176
rs541444637	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9315075	GCATTGCACTGGTTT[A/G]AAATACAACATCTTG	80176
rs541448718	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9324453	TGCACATCCCTGGCT[C/G]TCCTCCATGGTGTCT	80176
rs541569234	snp	C/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9313870	AATCTCCTGCTTTTC[C/T]CTATAGGAGTGAACA	80176
rs541599604	snp	A/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9350420	GGACGTGGTGACTAA[A/T]GCAAGAGTGTGCTTT	80176
rs541602895	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9323267	AAACATTCTAGTTCC[C/T]GCCGAGCCGAGGGGG	80176
rs541662106	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9323782	TGCTATGTCATTTTG[C/T]TGCTAGTTTCCAGGG	80176
rs541676586	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9313808	CTCAGTGAAGGCTGA[A/G]TGAATGGAGGAGTGT	80176
rs541718402	snp	A/C/T	0.00159649	0.0282165	intron-variant	SPSB1	GRCh38.p7	1:9299259	GGCAATGCCCCTTGG[A/C/T]GGTCTGGGCTGATGG	80176
rs541736712	snp	C/T	0.0298908	0.118541	intron-variant	SPSB1	GRCh38.p7	1:9299490	TCTCTCTCTCTCTCT[C/T]TTTTTGAGATGGATT	80176
rs541759635	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9351095	TGGGGTCGGCAAACA[A/G]CAGCTCCTGGGCCAA	80176
rs541784244	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9349502	GGCTGAGGCCTTGGC[A/G]CCAGCGCCGTAGATG	80176
rs541793084	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9292252	CTCTGTTCGGGGAAG[A/G]GGGAGGAAAATTCCT	80176
rs541821768	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9362961	CAGGCCACAGTGCAG[G/T]TGCCCACCCCCTCGG	80176
rs541824867	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9346117	GCTGCAGAGATTGAT[G/T]CTGATAAAATAGCAG	80176
rs541829957	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9295634	CTTCACCAGAGCTGG[A/G]GAATGGGGTGGGGGC	80176
rs541961931	snp	A/C	0.00755907	0.0610114	intron-variant	SPSB1	GRCh38.p7	1:9293098	GGGGCACCTGGGACC[A/C]CGATGGGTGGGCGAC	80176
rs541984418	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9328985	TAGTAAAATCACCCA[C/G]GTTGAAAACCACTGC	80176
rs541984907	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9356694	AGTGTTTTGAAGACG[A/G]TATTCCAGTGTATTC	80176
rs541996099	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9317919	CTTGGCACACCATTC[A/G]CTCCGCGAGTTTGTT	80176
rs542008211	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9341591	CACTTCTGCCGGTGA[C/T]ATCTTGTCCATGTTG	80176
rs542010662	snp	A/G	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9335733	TGAGCACTTGAGCCC[A/G]GAAGGTTGAGCCTGC	80176
rs542019781	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9361755	TGTCACTCTCCCTCT[C/T]TCTCCTGGAGGGCAG	80176
rs542061204	snp	C/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9329812	GGGCCGTGGGGATGG[C/T]AGGCTTGGGTGTGGA	80176
rs542085709	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9367066	GGAAGAGCAGGGATC[A/G]CCTGGGTTCGAATCC	80176
rs542119105	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9366442	TATGATTCAGGACAG[A/G]GTTTGCCATGTCTTC	80176
rs542144597	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9361337	CAGACCTGATCTGGG[A/G]CTTTGCTGTCTCTGT	80176
rs542144700	snp	A/G	0.00438332	0.0466095	intron-variant	SPSB1	GRCh38.p7	1:9340906	TGGCTGCGGTGCGGG[A/G]AGGCAGAGTGGGAAG	80176
rs542186544	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9324945	GGGACACCCGGCCTG[A/G]CGGGCTGGTGGATCG	80176
rs542188035	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9365342	GGCTGGTCTCAAACT[C/T]CTGGGCTCAAGCAGT	80176
rs542233520	snp	G/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9327095	GCATCTGCCGTCGTT[G/T]CGTGGGGAAGAGACT	80176
rs542296327	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9367594	TCGCCATCATACCGC[C/T]AGCGCGACAGCCACC	80176
rs542326329	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9364921	CGATGGTGTGATCTC[A/G]GGTCACTGCAACCTC	80176
rs542341970	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9300255	ATGCCTCGTGGGCCT[C/G]TTTGGACTTTGGAGG	80176
rs542343151	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9294957	GCCAGCCTGTCCTAG[A/G]GAGGCCCAGAGAGGG	80176
rs542386129	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9299334	ATCTTGATCACCTTT[C/G]CCTTCCACAGATATC	80176
rs542401514	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9305331	AGCCCTGCCATCCAC[A/G]GTCCACCCTGTCACC	80176
rs542407850	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9343566	TAACAAGACAACAGT[A/G]AAGAAGTTTAAAAGG	80176
rs542418446	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9338725	CCTTTTGAGGTCTGA[A/G]GGGGCGTCACCTCCC	80176
rs542494428	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9309152	CCAGGCCCAGGGGTC[A/G]TCGGTGGGCATGGGG	80176
rs542561321	snp	A/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9341586	TGGGTCACTTCTGCC[A/G]GTGACATCTTGTCCA	80176
rs542564386	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9304862	ATTTCTCACAAAGAC[A/G]GTGTCTCCCTATGTT	80176
rs542599659	in-del	-/ATTCTT	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9331638	GCCTAGCCGGCACTC[-/ATTCTT]ATGGGCTCACGCACC	80176
rs542634396	snp	C/T			upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291154	GGAGTGTTGCCATGT[C/T]GGCCAGGCTGGTCCT	80176
rs542720957	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9302258	GGATGTCAACTTGAC[C/T]AGATTAAGGAATACC	80176
rs542742625	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9307601	CAGTTGTAGAGGCCA[C/T]GTGAAGGTGGGATGG	80176
rs542746449	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9308236	TGCCAGTGCTGTTGG[G/T]GCAGTGCTGCAGTTG	80176
rs542807872	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9332522	GTCACTGCTGGGGAG[A/G]TGATATTTGGTGGAC	80176
rs542823469	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9310058	AGCTCTCCTCAGGTG[A/G]GGGATGGTGAGGGGC	80176
rs542832579	in-del	-/C	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9361544	GCATGCCAGGCAGAA[-/C]CCCCCCCGCAGCAGA	80176
rs542842577	snp	A/C	0.000798403	0.0199641	downstream-variant-500B	SPSB1	GRCh38.p7	1:9369588	AGAGACATAGCTGAC[A/C]CCTCCTGGGTCCAGC	80176
rs542901957	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9312445	ATTATGCACACGCCA[C/T]GCAGTTCGCCTATTG	80176
rs542938845	snp	G/T	0.00159617	0.0282053	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9367996	AGAGCAGATACCAGG[G/T]GTACTAAGAGGTGCT	80176
rs542991905	snp	A/G	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9354986	GTGCTGTTGAGACCC[A/G]GAGGGCGAAACCCTG	80176
rs543008775	snp	A/G	0.00478085	0.0486577	intron-variant	SPSB1	GRCh38.p7	1:9302622	GTACGAGTGGTCTCC[A/G]GAGTCTTTGACCTGG	80176
rs543019114	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9312561	CTCAGCATGCTGTGC[A/G]GTGGGGACTGGGGGA	80176
rs543031551	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9339801	GTTTATGTGCCCTGC[C/T]CCCCATTCTTGTGGA	80176
rs543033040	snp	C/G	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9322789	CTTGTTCTGGCCGGT[C/G]TGATGGTCAGCGGGG	80176
rs543057884	snp	A/T	0.00318978	0.0398085	intron-variant	SPSB1	GRCh38.p7	1:9328152	TTTACACCCCCTCCT[A/T]TAGAGCCAGACGAAC	80176
rs543094934	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9327036	TCTTGGCTTAGGGGC[A/T]GGTGCTCAGGGCAGG	80176
rs543095699	snp	C/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9313117	TAAAAAAAGTCAAGT[C/T]CGGGCGCGGTGGCTC	80176
rs543121608	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9327649	AGTCTTGGGGGAGTG[C/T]GGGGGAGAAATTTGA	80176
rs543157492	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9360669	CCCCAGGGTGCTCCA[C/T]CTGTGTATGTGTCTC	80176
rs543169618	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9344504	ATTCCCTGGCTGAGC[A/G]CTCTCCTGCACTTGG	80176
rs543208029	snp	C/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9333116	CACTCCATGGGAAAA[C/T]GGCCAGAAACATGGA	80176
rs543210046	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9339332	TGGTCTCGGGTGGGG[C/T]GTGGACTTCAGCTAG	80176
rs543222104	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9333586	TCCGCCCACCTCGGC[C/T]TCCCAAAGTGCTGGG	80176
rs543264432	in-del	-/ACAT	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9350044	GAAGACACACCACAC[-/ACAT]ATACACACATCCAGA	80176
rs543281527	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9354450	TCCTTGGCCTCTCTG[A/G]TCCCTTCCAGAGGCC	80176
rs543296066	snp	C/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9317112	AACTCACAAATAATA[C/T]ATTATACTAGGCAGA	80176
rs543333580	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9307147	TGGCCAGGCCGGTCT[C/T]GAACTCCTGACCTCA	80176
rs543356911	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9317924	CACACCATTCGCTCC[A/G]CGAGTTTGTTAAGGG	80176
rs543371623	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9361117	AGCAGAGCATGACAG[A/G]TGGAGGCTCTGGCCA	80176
rs543385990	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9301313	CTGAGCAACATAGTG[A/C]GACTCCCCGCCCCCG	80176
rs543412086	snp	A/C	0.000798403	0.0199641	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9292082	TGGTAAAGACACAGT[A/C]ACTACGGAAGCCCCG	80176
rs543420504	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9319101	GAGAATTGCTTGAAC[C/G]TGGGAGGAGGCAGAG	80176
rs543482410	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9366482	ATGGTTAGTGGCTAA[A/G]GGCATGGACGCTGGG	80176
rs543486854	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9317939	GCGAGTTTGTTAAGG[A/G]CCCCTGTGTGCCAGG	80176
rs543506332	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9365981	GGCGAGCAGGGCCGC[A/G]CAGCCTTCCAACGCT	80176
rs543630445	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9364984	AGCCTCCCGAGTAGC[C/T]GGGACTACAGGCCCA	80176
rs543679805	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9339854	CTGCCTGCTCCTTCC[A/G]TGGCACAGGTCGGCC	80176
rs543721689	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9307448	GTATTCTGATTTGAC[A/G]GGTTTGCCTGTGCTG	80176
rs543735666	snp	C/T	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9343978	TTTTAAAAGTAGAGA[C/T]GGGGTTTCACCGTGT	80176
rs543753104	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9349746	TTGTGTGAGGAAGGT[C/G]CTTTCGGGAGTTCCC	80176
rs543767481	snp	A/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9301568	ACAGGACACGGATAG[A/G]CCTCCCGAGTGCGCA	80176
rs543811314	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9317408	CTGACTCCAGGATTT[A/G]GTTTAGGTATCTGGG	80176
rs543813925	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9348204	CCCACCTCGGCCTCT[C/T]AAAGTGCTGGGATTA	80176
rs543845340	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9329094	GATGTGTAGGAGTTC[A/G]CGTGGGGGACAGGGT	80176
rs543847389	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9335556	GCTCACGCCTGTAAT[C/T]CCAGCACTTCGGGAT	80176
rs543881052	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9308440	GGTTGCCTCAGGCAC[A/G]AGAGAAAACCTAAGC	80176
rs543917134	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9304382	TTCCCCTAACCCATC[C/G]TTTCTCATCTGTCTC	80176
rs543921736	snp	A/C	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9301079	GTGCACCTTGCTTCG[A/C]AGGAGAGATGGCCAG	80176
rs543931093	snp	A/G	0.00358779	0.0422022	intron-variant	SPSB1	GRCh38.p7	1:9340264	GAAGGGGTGCTGTCA[A/G]TCAGCAGAGGAGGGG	80176
rs543974651	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9293925	GTGTGTTCATGTGGG[G/T]GTGTGTGTGAGTGTG	80176
rs544002122	snp	A/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9342596	GCCTTGTTCCCAGTG[A/T]AGTGATCACCCTGAC	80176
rs544085256	snp	A/C	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9318425	GGACAGCGTCCTCTC[A/C]TATCGCCCACGAAGC	80176
rs544088318	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9357869	CAGAGTTCCTTGCCT[A/G]CATGAGTCCCTTCTA	80176
rs544089494	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9347827	ATGGACAGGGACTGC[C/T]TCGTTGTACCTGCAC	80176
rs544108805	snp	G/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9300251	CACAATGCCTCGTGG[G/T]CCTGTTTGGACTTTG	80176
rs544135093	snp	A/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9313213	ACCAGCCTGACCAAC[A/G]TGATGAAACCCTGTC	80176
rs544166670	snp	C/T	0.00159617	0.0282053	downstream-variant-500B	SPSB1	GRCh38.p7	1:9369560	TCCTCGTTTGTGCCT[C/T]GGGGGAGGGGAAAGA	80176
rs544242014	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9348926	GGACATCCCCTTTCA[C/G]TCGTGCAAGAATGTG	80176
rs544277884	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9306033	TTAGGGAACGAAGGC[A/G]TGTTGGGGACAGAGC	80176
rs544315866	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9316998	GGCCTCACCTTGGAT[G/T]CACCTTCCTGCTTCC	80176
rs544355943	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9347412	AGTTTGAAAAGGAAT[A/G]CATGCATTTTAAAAA	80176
rs544374061	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9353582	ACTGGACACAAGGAG[C/T]CCTGCCCTGCTCTGA	80176
rs544459881	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9326364	CTGGGCCCCGTGGAA[G/T]CTCTTGGAGTCTCTG	80176
rs544527945	snp	A/G	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9315759	GCCCCACCTACGGAG[A/G]GACCGCACTGCTCAC	80176
rs544536804	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9296832	GGGAGGATGGCAAAA[C/T]CCAACAGCACATTGG	80176
rs544566145	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9369302	GATGAATGTTTCCCT[C/T]GTACAGATCCCAGCT	80176
rs544679302	in-del	-/TTTG	0.00438944	0.0466418	intron-variant	SPSB1	GRCh38.p7	1:9332229	AGCGTTTTAGGAAGA[-/TTTG]TTTGAGTGGGCTGAG	80176
rs544703864	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9353850	TTGAACCCAGGAAGC[A/G]GAGGTTGCAGTGAGA	80176
rs544712634	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9369388	GCATCTCCCACCCCC[C/T]GACACCCTGGGACCC	80176
rs544748653	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9329017	CTGTCCTACTAGGGG[C/T]GGGCCCTGCATTTGC	80176
rs544764581	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9348288	GTCTCGCTCCTGTCT[C/T]GGCGGTAGTGCTGTG	80176
rs544771263	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9314826	AAACTCACATGCCCC[C/G]CGGGGTCAGGAAGGA	80176
rs544772763	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9344957	AGTGTCACTGGCTCC[C/G]ATTCAGGCCTTGGCA	80176
rs544812544	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9338202	TGCCACTCAGCTCTC[C/T]CCTACCCCGTTTCTT	80176
rs544857428	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9320821	AAATTTATGTCACTG[A/G]TGGTTTGGAAGCTAC	80176
rs544858166	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9326032	GAGTGTGGGCTCCAT[G/T]AGGTCAGAGTGACCT	80176
rs544885454	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9332329	TGGGATTCAGCAACT[A/G]TGGGGGCAGCAATTT	80176
rs544931393	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9358591	GAGGAGCCCTGACCC[G/T]CAGCCCTGCCTCCCT	80176
rs544942120	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9316410	TATGTGTGTGCATAT[A/G]TGCTTGTGTGTGTGT	80176
rs544995758	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9306468	ACAATAGCCATCAAC[A/G]ATGTGGCATATCTGA	80176
rs545022181	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9332482	GGCCATTTGAGTCTA[C/T]AAGGGATGTATGAGT	80176
rs545032860	snp	C/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9326405	AGAAAAGTCAGTGGG[C/T]GGTGTCGGAGGAGTC	80176
rs545033321	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9332980	CCCCATCCTGGGCTC[C/T]GTGGCTGAGACTTGG	80176
rs545067032	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9301601	GGACATGAGGTATGT[G/T]GGTAGGATGACCTAG	80176
rs545100336	snp	A/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9322337	TCTCAGGTTATAGCC[A/G]GTAAGGGCAGAGCTG	80176
rs545103641	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9307185	TGCCCGCTTTGGCCT[C/T]CCAAAGTGCTGGGAT	80176
rs545104001	snp	C/T	0.00358779	0.0422022	intron-variant	SPSB1	GRCh38.p7	1:9306712	AAGAAATGAGCGATC[C/T]GAGAGATAGGTCAGC	80176
rs545145918	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9342665	GGGTCATCCCCTCCC[A/C]AGACCACAGTTTGGG	80176
rs545169408	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9305528	GGAGTAGGTAAGACC[A/G]GTGGCGTAGTGGATC	80176
rs545257746	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9322044	GAATCACACTGGGCA[A/G]GTGATGTAAATATGT	80176
rs545402387	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9345587	CGCCACCCTGACTAA[C/G]CTACAGCTGCGATAT	80176
rs545436071	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9309585	CAGTGGCTCACGCCT[A/G]TAATCTCAGCACTTT	80176
rs545460646	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9314446	TGAGCATCTAGACCC[C/T]GACTGCCAACCCACC	80176
rs545500492	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9315009	CCAGACTTTTTAAGA[C/T]GTTGGCAAATAATTC	80176
rs545501198	snp	A/G	0.00914312	0.0669923	intron-variant	SPSB1	GRCh38.p7	1:9348965	TGTGTGTGTGTGTGT[A/G]TATGTGCGTGTGTGC	80176
rs545509289	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9305666	TTCCTTCCATGCCCC[A/G]TGGGAGGTCAGGAAC	80176
rs545624668	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9346144	GCAGATTGCTCGGGG[C/T]ATGTTTCTCTTGCAA	80176
rs545655091	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9321530	GCGTGCCAAGGATTC[A/G]GCTCAGAACGGGGAA	80176
rs545673547	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9297568	ATATTAGGATGTGGA[A/G]CGAACATGAAGTTGG	80176
rs545686777	snp	G/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9299775	TGAGCCACTGCGCCC[G/T]GGCCGACATCATCTC	80176
rs545690644	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9293145	GGCGCGGGGGGCCGG[A/G]CGAGGGCGGACGCGG	80176
rs545691018	snp	A/C	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9326931	GGCGGGGACCCTAAC[A/C]CCTTCTTTCCTGCTT	80176
rs545727663	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9294120	TGTGTGTCTGTGTGT[A/G]AGTGTGTATGTGTCT	80176
rs545751370	snp	C/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9323824	ACATTTCTTCTGCTG[C/T]TGCCCACGGACGGCA	80176
rs545762018	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9352467	GGAACTCAGCCACGC[G/T]CGTTTATTTATGTCC	80176
rs545771850	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9296157	CCTAAGCATAATAAT[A/G]GCGGGAAATGGTTTC	80176
rs545802327	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9341728	TTTTTTTGAGACGGG[A/G]TTTCACTCTTGTTGC	80176
rs545804093	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9333050	GCCCTCGTGGGCTGC[A/G]TCAGGCACCCAGCAA	80176
rs545847815	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9358376	GGGACTCCTGGAAGA[A/G]GTGGGTGACCAGGCC	80176
rs545957643	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9302430	TGGAGGACACTGGCA[A/G]TTGAGTCACTCAACT	80176
rs545960815	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9324318	ATCGTGTCCCGATTA[C/G]CTGTTGGTGGTGTGC	80176
rs545966704	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9351627	TGGCGAGTCCAGCTC[C/G]TGGGGACCCGCAGAA	80176
rs545982053	snp	C/G	0.00398564	0.0444627	intron-variant	SPSB1	GRCh38.p7	1:9330570	GCTGGACCTTGTGAT[C/G]TGGACACACGTATCC	80176
rs545986642	snp	A/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9363704	TGCAGTTTTAGAAAA[A/T]TTTTTTTTTTTTGGA	80176
rs545991315	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9356782	CTAGATTACCTAACG[A/G]TGCCTCATGAATGAA	80176
rs546024185	snp	A/G	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9319623	GGTGGCTGATGTTCC[A/G]TACCGGGCTGGTATT	80176
rs546075063	snp	C/T	0.00478085	0.0486577	intron-variant	SPSB1	GRCh38.p7	1:9336925	ACCTGGCACCTCCCC[C/T]TCTGGTGCCTGCTGG	80176
rs546083560	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9362227	TGTCGGGGAGGGGTT[A/G]TCCCAGACCCTATTC	80176
rs546139728	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9307175	TCAGGTGATCTGCCC[A/G]CTTTGGCCTCCCAAA	80176
rs546163289	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9320621	CAAGTATTTGGAGCA[A/G]TGGAGCAGGAGAAAC	80176
rs546190896	snp	A/G	0.00358779	0.0422022	intron-variant	SPSB1	GRCh38.p7	1:9324659	TGTCTTGTTCCTATA[A/G]AGGGCACTTTGTGTG	80176
rs546201485	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9305945	GGCCAAAATGAGTGC[A/G]GAGAGGCAGGAGGGC	80176
rs546215741	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9342267	GGCTGTGCCAGGCCT[A/G]TGAGTGACGATCCCT	80176
rs546248981	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9325321	AGGGACAGTCTGGGC[C/T]GTGTGGGATTGAGCT	80176
rs546253365	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9305035	TTCACCTGCCTCCTG[C/T]GCCCAGACCCATCTG	80176
rs546273010	snp	A/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9363129	CGGCACGAAGCCCAC[A/G]TCTGTTTCTGTGGCC	80176
rs546317180	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9295669	CCCGTGGAAGCCAGC[G/T]CTGCCCTCCCACCCC	80176
rs546317782	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9300333	CACCCTAACGCTTCT[A/G]GTTTTGAGTGGGGCC	80176
rs546378698	snp	C/T	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9295084	ATGGGCCAGGCACTT[C/T]GTGTCTCCCCAGCTG	80176
rs546414913	snp	A/G	0.0333695	0.124785	intron-variant	SPSB1	GRCh38.p7	1:9309263	TGTGCTCCCCTGCGG[A/G]GAGAGAGAGAGAGAG	80176
rs546437410	snp	A/G	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9304625	AGGGTGAAGAATTGC[A/G]GGTGCCTCGGGTTCC	80176
rs546450090	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9368127	ACCAAGAACTGTCTG[C/T]AGGCAAATAAGCACC	80176
rs546492037	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9300306	TGTGTTACTCCAGCC[C/G]ATTTGCTGAGTCACC	80176
rs546541493	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9342450	AGAGCACGGAGGATC[C/T]CAGTGGCTTGTCAAT	80176
rs546563687	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9330016	CATTTTTGCAAAGAG[C/G]AAAAGGGAAACCTGA	80176
rs546602730	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9342712	ACACATCCGAGATGC[A/G]GGCACACATCCCGGA	80176
rs546614802	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9294708	GACTAAGGTTTGATG[C/T]CCTTGGAAGAATTTT	80176
rs546620077	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9351186	ATTTACATATTGTCC[A/G]GAGAGCCTTAAGTAG	80176
rs546656325	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9362402	TTGGCTGTGCTCTTT[C/T]GTAAGAACTGCGTAG	80176
rs546700537	snp	A/G	0.0360663	0.129354	intron-variant	SPSB1	GRCh38.p7	1:9335899	ACCCTCCGAATGTCA[A/G]TGTGCACAGTAGTAA	80176
rs546741833	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9367228	CTGTGAGGATTAAAT[A/G]AGTGTTAGCAGAGGG	80176
rs546744759	in-del	-/G	0.0341408	0.126114	intron-variant	SPSB1	GRCh38.p7	1:9309228	TGTGCAGATAAGCTA[-/G]GATCCCCCCTCAATT	80176
rs546751272	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9316019	AGAGGTGGAAATTGC[G/T]TAGTCATTTGCAAAC	80176
rs546755351	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9352518	CGACAACAGCAGAGA[C/T]TGTCTGGCCCTCAAA	80176
rs546767860	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9320296	CATCAGCCATTATTG[A/C]CTCTTGGGCCGGGAC	80176
rs546768334	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9340568	GAGGACCTTGGTCCT[C/T]CTCCAGCTGTGGAAA	80176
rs546791808	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9310354	ATGTGAGGTTCTTGG[A/G]GCGCCTTCCTGGATT	80176
rs546835783	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9341220	CCGGCCTCAGAACAG[A/G]GAGGCACGGTACACA	80176
rs546846861	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9314044	AGCCAGGTGTGGCGG[C/T]GGGCACTTGTTATCC	80176
rs546855699	snp	C/T	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9325002	GGGTAGGCAGCCCCA[C/T]TGGGAGCCACAGCCA	80176
rs546943909	snp	C/T	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9344166	TGAGATTCTAAACTG[C/T]TGAGCCATAATTCCT	80176
rs546954537	snp	C/G	0.00795532	0.062565	intron-variant	SPSB1	GRCh38.p7	1:9345742	TTTGGGTCTTTTGAG[C/G]TCAGGGACTAGAGCT	80176
rs546989900	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9337388	AGGAGTGTGGCCAGG[A/G]CAGGCACCTCACACC	80176
rs547005113	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9344606	GGAGCAGCATGTATG[A/G]AGCTCTTACTTTGTG	80176
rs547069437	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9349077	GTCATCTGGTGTCCC[C/T]GCAGGTAGCCCCTCC	80176
rs547135616	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9352082	TGGGCTGGGGTGAGG[A/G]GGTGGAGGGAAGGTG	80176
rs547159081	snp	A/G			upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291437	TGATCCGCCCGCCTC[A/G]ACCTCCCAAAGTGCT	80176
rs547199795	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9310892	GGGGGCCACAGCGTG[C/T]TTAATTTATTCCAAT	80176
rs547202116	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9322863	AGGCACCTCCAGCCC[A/G]CACCCACCCCACCCG	80176
rs547207002	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9315408	CAAAGCTTCTTGTGT[C/T]GTTGTCTCACGCAAG	80176
rs547236623	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9309550	CCCTTGCATTTAAAA[C/T]GTGGTAATCAGGCCA	80176
rs547334682	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9334570	AGTGGCATTAGGTAC[C/T]TTCATATTGTTGTAC	80176
rs547369082	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9305911	CCAGGTTGGAAAGGC[A/G]GGAAGGGTGCCCATG	80176
rs547404769	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9312695	TTGGATGATTGTGCA[C/T]GGACTCATCTCATCA	80176
rs547430971	in-del	-/G			intron-variant	SPSB1	GRCh38.p7	1:9316556	GCTGGATGGCGAGGA[-/G]GGGGGGGGCTGATCG	80176
rs547443975	snp	C/G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9319898	GGGAAGCAGCCTCCC[C/G/T]GCCTATCTAGCCCCA	80176
rs547444831	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9310954	GGGTTCTTCTAAAAA[C/T]ACTTCGCCATCTTTG	80176
rs547466382	snp	C/T	0.00597247	0.0543191	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9292606	GCCCTGCGCCACGCG[C/T]TTCCCAAAGACGCCT	80176
rs547484598	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9361565	CCGCAGCAGAGTCCC[A/G]GCTTCTACACTGGGG	80176
rs547495073	snp	C/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9361927	GTGGGTCCTCTGGCT[C/G]TACCCCCACTGCTTT	80176
rs547540056	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9360752	ACCCCAATCCACTAT[G/T]CCCTCGTCATAATGA	80176
rs547576855	snp	C/G	0.000399281	0.0141238	utr-variant-5-prime	SPSB1	GRCh38.p7	1:9355815	CTGTCTGGCCCCGAT[C/G]AGAATACTGGAGACG	80176
rs547592634	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9336522	TGAGCCACCACGTCC[A/G]GCTCCTCCTCCTGGT	80176
rs547618417	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9366229	CCCATGTGCCTGGGG[A/C]AGTTGCGGGGAGAAG	80176
rs547628289	snp	C/T	0.0123036	0.0774623	intron-variant	SPSB1	GRCh38.p7	1:9366158	GCAGCTGGAAGCGCT[C/T]TGTAACCCTGGGGCC	80176
rs547645672	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9297964	CAGCCCTTACAGTGG[A/G]AGCCGCAGTCACTCA	80176
rs547709390	snp	A/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9365044	CTAATTTTAGTAGAG[A/T]TGAGGGTTCACCATG	80176
rs547744191	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9340113	GATGGTCTGTGGGCC[A/G]CCCTAGGGTCACCGG	80176
rs547789698	snp	A/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9323854	AGGGGCTGTGCCATG[A/T]GGGACCTTGGAACCC	80176
rs547798680	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9334714	CCATTCCTGCTCCCC[A/G]GAGCTCCTGGCAACC	80176
rs547801123	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9333950	CCTTCTCATTTTTTT[A/G]CTTTTGTCCCAGTAG	80176
rs547804832	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9311399	AGATTTTTATAATGG[A/G]AAATTTCAAACACAG	80176
rs547842418	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9327591	GGGGAGCAGCTGGCC[A/C]CTCCAGTGCACCAGG	80176
rs547874623	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9323409	CTGTGGAGCCTCCCT[C/T]GCGGCCCGTTGGCAG	80176
rs547948414	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9307832	TCCCATTGCTATTAC[A/G]GTGAATTTGTAAATC	80176
rs547961557	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9318053	GCTGCACTCATTCCC[C/T]TTTCCGGGCAGGTTG	80176
rs547970612	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9364595	GTCTGTGGGATCCTT[A/G]ACCTTAAAGAACCCA	80176
rs548012360	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9328626	TGGGGTGAGCACCAA[C/T]GCCCCACCCACTGCC	80176
rs548018758	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9348298	TGTCTCGGCGGTAGT[A/G]CTGTGTCTAGCATCA	80176
rs548021929	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9318622	GTGAGACTTACCTTG[C/T]GGAATCGTGCAGGAT	80176
rs548046121	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9322921	TTGTTGTCTGGCTGC[A/G]TCAGACGTCTGGGCT	80176
rs548099922	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9340012	AGCCCTGAACCACCT[A/G]GGCATGCAGGTCACC	80176
rs548118612	snp	G/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9312737	TTTTGGTTTTCTTTG[G/T]GTTTTATTATTATTA	80176
rs548256080	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9304074	TCCAATCAGCTGGTG[A/G]CCTGGATGGAACAAA	80176
rs548265875	snp	A/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9362319	TAGGGGACCAAGGGT[A/G]TCTGATCACCTAGGT	80176
rs548275117	snp	C/T	9.89201e-05	0.00703209	synonymous-codon	SPSB1	GRCh38.p7	1:9356443	AGCCCTGGACATGGA[C/T]GACGGGACTCTGAGC	80176
rs548289646	snp	A/G	0.00279162	0.0372561	intron-variant	SPSB1	GRCh38.p7	1:9327176	CCCTCTAAGCCCACG[A/G]CCTCCACAGTGGCCA	80176
rs548318957	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9338947	TCTGGAAAACCCGGC[C/T]GATTACCTTGTAATT	80176
rs548331121	snp	A/G	0.00013433	0.00819431	missense	SPSB1	GRCh38.p7	1:9367516	GGGAGGGAGCGCCTG[A/G]GGGAGATCCACACGC	80176
rs548361383	snp	G/T	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9324548	TGAGGAAACCAGCTT[G/T]GGTGGGGAGGGGGAG	80176
rs548492519	snp	A/C	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9360816	CTCCACTCTGAAGTT[A/C]TGGGCAAACATGAAT	80176
rs548499692	snp	C/T	0.00557542	0.0525036	intron-variant	SPSB1	GRCh38.p7	1:9335121	GAGGAATTGCCGTAT[C/T]GTTTTCTACAGGGCC	80176
rs548528986	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9350592	TGTGCATGTGTGTGC[A/C]TGTAGGCATGCGTGC	80176
rs548551698	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9366302	TTCCAGTTTCCTGGG[G/T]CCTGAGCTTGGCCTG	80176
rs548559600	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9331812	TCTGGAGGGTGCAAC[A/G]TGCGATCTCATTACT	80176
rs548597368	snp	A/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9314125	AGGTTGCAGTGAGCT[A/G]AGATCGCACTACTGC	80176
rs548620808	snp	A/G	0.00438332	0.0466095	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9292676	GCGGCTCGGGAGAGG[A/G]CTGCGGACTAAGGGG	80176
rs548630925	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9328658	CCCTCTGGCCTGGGA[A/G]AGCCATGGAGTTGAC	80176
rs548634292	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9314744	GGGACACTTCCTGTG[A/G]CCATTTCTAGTGGCA	80176
rs548664354	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9360241	CCCAGTAGATTTTGG[A/T]GTCCTGGATGCCAAG	80176
rs548664360	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9353949	AACCCTGTGTCTCAC[A/G]TCAGAAAGGGGAGGG	80176
rs548667209	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9364563	GGGTGGAACCCAGTC[C/G]CACCCCATCACGAGG	80176
rs548679810	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9359330	GATAGGGTGAGGCGC[A/G]GGTGTTAGCGCTGCC	80176
rs548755959	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9329221	GGCCCGAGCACAGCC[A/G]GTTGAGGGTTTGTGG	80176
rs548769237	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9323897	ATCCCTTCCTCTTAT[A/G]TCTGCCCTCTCTGTG	80176
rs548792246	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9364073	AACTCCCTCTCAGCC[C/T]TCACTGCTGCAGCCT	80176
rs548863652	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9296453	TGAAATTTTTTGTTA[C/T]TATGGAAAATGTCAA	80176
rs548877449	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9366614	GAGTCTTGCTCTGTC[A/G]CCCAGCTAGAGTGCA	80176
rs548886812	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9304526	GGTTCATATCCCTGA[C/T]CTGCCAGTTGGGATG	80176
rs548911930	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9295292	AGGCAATCACTTTAC[A/T]AGTCTTCCTTTTCCA	80176
rs548957396	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9303837	ATTTCAGATGTCAAC[C/T]TGACTAGACTAAGGA	80176
rs548968975	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9322320	CTGAGGTTCGGAAAG[G/T]CTCTCAGGTTATAGC	80176
rs549021124	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9368856	AGAGCCTCAAGAGGG[G/T]TAGCTCGGCTGCCGG	80176
rs549030892	snp	A/G			downstream-variant-500B	SPSB1	GRCh38.p7	1:9369706	GACAGAGAAGGAGAA[A/G]GAGAGTCCTGGAGGG	80176
rs549039191	snp	C/G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9337778	CTCCCTGCCTCCGTT[C/G/T]GTTCTCTTGCTCCCT	80176
rs549052543	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9302499	TCCAGTCAGCCGGGG[C/G]CCTGGAAGAAGGGTG	80176
rs549064260	snp	A/C	0.00478085	0.0486577	intron-variant	SPSB1	GRCh38.p7	1:9326578	TGCTCTGAGTGGGAC[A/C]TGGGGTGTGAGTCTG	80176
rs549066242	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9321119	TTCTACCCCTCCCCC[A/G]AAAAGAAAACAACAA	80176
rs549102175	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9327291	TGTTTCATAATGTAT[A/G]TAATCTATCGATACA	80176
rs549176198	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9305650	CGTTCTCAGACCAGA[C/T]TTCCTTCCATGCCCC	80176
rs549212148	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9307267	TCACATAATGTAAAA[C/T]GAGCCATTTTAAAGT	80176
rs549214058	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9302088	GTGCAGGGAATTGGC[C/T]GGTGAGCACGAGCCC	80176
rs549239201	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9333272	GTCTTATATGCATTT[A/G]TCTCCTTTTTCAAGT	80176
rs549277498	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9307020	GCAGCCTCCGCCTCC[C/T]AGGTTCCAGTGATTC	80176
rs549290618	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9331244	AATGACTGTGCACTC[G/T]ATTTGGAGTGGCAGG	80176
rs549304734	in-del	-/A			intron-variant	SPSB1	GRCh38.p7	1:9299964	TAAGACCCTGTCTCA[-/A]AAAAAAAAAAAAAAA	80176
rs549319962	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9301637	TTCTCGTCAGCCTCT[C/T]TCCCTGGCCACCCCT	80176
rs549351890	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9333863	CGGGGAAAACAGCTC[A/G]AGGTAGAGAGGACCT	80176
rs549364276	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9328001	TGGATGGTGAATGGA[C/G]TGCTGCAATCACACT	80176
rs549384531	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9365636	ATACCCATAAGCAGC[C/T]TCTCTCCATTCTGCC	80176
rs549388193	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9348717	CCTGGACCCAGACAA[C/T]CTTAAATGGCTGTTC	80176
rs549424672	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9360213	GAGGCCAGGAGGGTG[A/G]GGGCTGAAGGGACCC	80176
rs549438556	in-del	-/T	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9337925	AAGAGAGTGACCTGG[-/T]TGGCTCTTCCGGTGA	80176
rs549460972	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9354106	TCTTCCCAGCTGAGA[C/G]GGAGCTCTAGGCCAG	80176
rs549514808	snp	A/G	0.00279162	0.0372561	intron-variant	SPSB1	GRCh38.p7	1:9365103	CTCAGGTAATGCGCC[A/G]GCCTCGGCCTCCCGA	80176
rs549551697	snp	A/G	0.00358779	0.0422022	intron-variant	SPSB1	GRCh38.p7	1:9338550	CCTCGCCCAGGAGGA[A/G]GTATACTTTCTTCTT	80176
rs549586723	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9324912	CTTTCTTGGAAAAGC[A/G]AGTGGGGTGGGGGAG	80176
rs549613058	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9338942	AGGACTCTGGAAAAC[C/T]CGGCCGATTACCTTG	80176
rs549623292	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9322685	GACCACCTGCAGGTT[C/T]CACTGTGGCTGGAAT	80176
rs549662472	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9311762	CGTGGCTTTATCTAC[C/G]ACGTTTTGTGTGTTT	80176
rs549689135	snp	G/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9348973	TGTGTGTATATGTGC[G/T]TGTGTGCACGTGCAT	80176
rs549698007	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9332556	TCAGGTTCACAGGCA[C/G]ACACTCCCTGGAGCC	80176
rs549765281	snp	A/C	0.000399281	0.0141238	downstream-variant-500B	SPSB1	GRCh38.p7	1:9369692	CAGGCAAAGCCCCAG[A/C]CAGAGAAGGAGAAGG	80176
rs549790235	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9318823	ATAGTGGGGGACAGT[C/T]ACATGAGCTGGTGAT	80176
rs549796114	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9311479	CACCAACAAATATTC[A/G]CTGGTCTCTTCACCA	80176
rs549823676	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9364651	TCCAATCAGAGCTCC[C/T]CTTAATCATCCTAAG	80176
rs549840317	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9359990	GGGGGCTGCTGACCC[A/G]AGATGGGAAAGCCCA	80176
rs549856944	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9348790	CTTAGAGCCCAGGCT[A/G]CCACCGAGAAATCCA	80176
rs549857361	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9316918	ATAAGAGTGCCCCCG[C/G]GTAGAGGGAGCTGCC	80176
rs549870769	snp	A/G			synonymous-codon	SPSB1	GRCh38.p7	1:9356359	CGATGGCAAGAACCA[A/G]CCAAGCAAAACATAC	80176
rs549884723	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291887	TCCGTAATCCTATTC[A/T]GAGTTCAAACAAAGC	80176
rs549938549	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9316113	CTGCTGAGGGCACCA[C/T]GGTGGTCCTGTGTTC	80176
rs549957035	snp	C/T	0.00478085	0.0486577	intron-variant	SPSB1	GRCh38.p7	1:9327113	TGGGGAAGAGACTAG[C/T]ACAACCCCCAGTGCC	80176
rs549962691	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9365737	AAGAACTTTAATCCA[C/T]TTTTTACTGGTAGGA	80176
rs550002361	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9298128	CTGACTTGTGTGGAT[A/C]TATGGCATTGGATAG	80176
rs550085751	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9296581	TGCTCACAGAAGATG[C/T]GCACATGTGTACACA	80176
rs550097839	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9348638	ACTGGAGGGATTTGC[A/G]AGGTTCTTTTCTTCC	80176
rs550122323	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9297263	TGGAAAACTAGGGAG[A/G]CATTGGGTGATTTGA	80176
rs550134473	snp	A/G	0.00279162	0.0372561	intron-variant	SPSB1	GRCh38.p7	1:9350141	CCCGCACAGGTACAC[A/G]CACACATTCTTTCTC	80176
rs550158346	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9323282	CGCCGAGCCGAGGGG[G/T]GCTGTGGCTCCACTG	80176
rs550193582	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9328579	AGAGGTAAACATCTC[A/G]TTCGGGGTAACCCAG	80176
rs550266838	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9366084	ATGAACTCAGCCTCC[C/T]TTGTAGGAAGGCAAG	80176
rs550302064	snp	A/C	0.00438332	0.0466095	intron-variant	SPSB1	GRCh38.p7	1:9330994	GAAGGATGATATACC[A/C]AGAGTAGTTCCATAC	80176
rs550310879	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9339418	AGGTAATTCCGGGGC[A/G]AGTCTGGAGGCGACG	80176
rs550329977	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9334339	GATCCGCCCGCCTCA[A/G]CCTGTCAAAGTGCTG	80176
rs550334592	snp	C/T	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9363468	TTCACAGGGGATGGA[C/T]TGTGGCAGCTGGAGG	80176
rs550360574	snp	A/C	0.00716266	0.059414	intron-variant	SPSB1	GRCh38.p7	1:9333413	TCGGCTCACTGCAAC[A/C]TCCGCCTCCCAGGTT	80176
rs550396316	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9303042	TGCCACCTGGCTTCT[C/T]TGGGCTCCCTGTGCC	80176
rs550407001	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9300144	CCCTTAGTGAAATTT[C/T]TCGGGGTCCAGTAGT	80176
rs550436845	snp	C/T	0.00358779	0.0422022	intron-variant	SPSB1	GRCh38.p7	1:9366770	GTAGAGACGGGGTTT[C/T]ACCATGTTGGCCAGG	80176
rs550464010	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9312620	GCTGATGGTAACACA[C/G]TCAGGTGCCAGCACG	80176
rs550518231	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9337854	GCTGCTCTAGCCGAA[C/G]ATCAGCATGGGGAAA	80176
rs550545477	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9305582	ATGTGGGCCCAGGGT[C/G]TGGGTGCTGGGGGTG	80176
rs550546054	snp	C/T	0.00636936	0.0560724	intron-variant	SPSB1	GRCh38.p7	1:9325073	TGCAGTGGCTGCACT[C/T]GCTGGAAGCTGGGAC	80176
rs550585431	snp	C/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9338407	AGGCTATCCTGGCTG[C/T]GCCTAAGGCCCCTCC	80176
rs550629958	snp	A/G	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9357740	ATGCAGCCCATGTGT[A/G]GGGGCACCGTGCTGG	80176
rs550649233	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9346779	GGGCCACCTCACCTG[A/G]CCTTTGCCACATGCA	80176
rs550666383	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9362857	TGATTTCTTTGCTGC[G/T]CATTCAGCATTGCAC	80176
rs550752431	snp	A/C	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9336141	GAGCAGTGCTCTCTC[A/C]TGTTGTTGGTTTGAA	80176
rs550756171	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9341838	CTCCTGAGTAGCTGG[A/G]ATTACAGGCATGCAC	80176
rs550783461	snp	C/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9348007	TCGAGTGCAGTGGTG[C/T]GATCTCGGCTCACTG	80176
rs550815755	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9336656	CGCTGCCTGAGTTCA[C/T]CCGTGGCGCTGGGCT	80176
rs550830865	snp	C/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9320741	GGCTCTGGCTGGCCA[C/T]GACCTTCCTTTTGAA	80176
rs550836161	snp	C/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9346403	GTGACAGACCCACCT[C/G]TGTGCATCCTTTACC	80176
rs550844501	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9342724	TGCAGGCACACATCC[C/T]GGACTCCTCCGGAGA	80176
rs550875482	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9294936	AAGTCCTGTCTTACT[A/G]TCTAGGCCAGCCTGT	80176
rs550910048	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9313387	CCTGGGCAACAAGAG[C/G]GAAACACCGCTCTTC	80176
rs550914241	snp	C/T	0.0718919	0.175435	intron-variant	SPSB1	GRCh38.p7	1:9306940	TTCTTCTTTTTTTTT[C/T]TTTTTTAAGTGGAAT	80176
rs550941813	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9341241	ACGGTACACACACCA[C/T]TCCCCACCAGGGCAC	80176
rs551024020	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9306257	CTCTGGGCCTTCCTA[G/T]CCGCGTCCTGCAGCA	80176
rs551039925	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9301677	TGGTGGGCTCAGGAA[C/T]AAAGTGGTCATGGTG	80176
rs551040494	snp	C/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9342467	AGTGGCTTGTCAATT[C/T]GCTGATAGCAGAAGG	80176
rs551059531	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9358756	CCCTGTGCCCTCCAG[A/G]AACATGCCCCCTGAT	80176
rs551119936	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9327305	TGTAATCTATCGATA[C/G]AGAAGCATGTGAGTA	80176
rs551168728	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9353197	CGCCTCAGCCCGCCC[A/G]GCCCCTCGAGAGCCG	80176
rs551195365	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9368428	GCGGGCCCCTCAGGG[A/G]GAAATAGCCTCACGT	80176
rs551231518	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9355593	GGGGATTTCATTCTG[C/T]GCCAAGGCTCCAGCC	80176
rs551247510	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9337292	AGAGTGGAGGACAAG[A/C]GTTGGCCCTGAAGTC	80176
rs551362942	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9326746	CCTCCCACTGGCGGA[A/G]CAGAAATGGTAAGCC	80176
rs551383446	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9333183	TTCAGTGTCTGCTCC[C/T]AGAGGGACCAGCACA	80176
rs551392369	snp	A/G	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9306134	GGGGGTTGCTAGAGG[A/G]CGAGCCTCACCCTTG	80176
rs551426037	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9306986	AGGCTAGGGTGCAGC[A/G]GCACAGTCTCAGCTC	80176
rs551449877	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9337043	TTCTAGCTCTCTCTG[A/G]CATCATTGCCCCAAA	80176
rs551452212	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9363526	TCAGACCTTGGACCT[A/G]TAACTCTCACCTCCC	80176
rs551537775	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9306026	TCGTGCTTTAGGGAA[C/T]GAAGGCGTGTTGGGG	80176
rs551538560	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9325624	AGGCACTGTGCCAGC[A/C]CCTGAGGCACAGTGT	80176
rs551550035	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9310976	CCATCTTTGGAAAAA[C/T]GGAATGTTCAAAAAG	80176
rs551584674	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9306551	CGTGATACCTATAGG[A/G]TAGGTACTACCCATT	80176
rs551585391	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9302030	GTAGCACTGCTTCCA[A/G]GGAGCTCACTTCACA	80176
rs551612321	snp	A/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9338522	GCCCTGGCCACTCTC[A/T]TGCCAGCTCCGGCCT	80176
rs551618444	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9301570	AGGACACGGATAGAC[C/T]TCCCGAGTGCGCACA	80176
rs551619998	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9305657	AGACCAGACTTCCTT[C/T]CATGCCCCGTGGGAG	80176
rs551636442	snp	A/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9341982	GCTGGGATTACAGGC[A/G]TGAGCCACCACGCCC	80176
rs551658883	snp	C/T	0.00318978	0.0398085	intron-variant	SPSB1	GRCh38.p7	1:9300394	GCTGTGCAACCTGCT[C/T]TGCCACTTGGGCCAC	80176
rs551699199	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9343340	CCTGGTCATTTCGTC[A/G]AAAGGGAATCGTACA	80176
rs551700802	snp	A/G	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9336664	GAGTTCACCCGTGGC[A/G]CTGGGCTAGTGAGGA	80176
rs551711318	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9338856	CCTGAATGGGATGAG[A/G]GGGTCTTTGGGTCTT	80176
rs551770668	snp	C/T	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9307586	TTTCCCGTCCTGGCT[C/T]AGTTGTAGAGGCCAC	80176
rs551780231	snp	A/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9335790	TCCAGCCTGGACGAC[A/T]GGGCAGGACCCTGTC	80176
rs551807474	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9322453	CTGTCCCAAAAGGCG[C/T]CTGCTCACCTGCACG	80176
rs551823471	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9308843	ACTGCGACAGTGGAA[C/T]GTGCCAGTCCTGTTG	80176
rs551835014	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9364719	AAAATACAGAACATT[C/T]CAGTTCCTTGTCAGG	80176
rs551844578	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9341030	TGTCTCTTCCTCCTC[A/G]GGCCCTGATTGCTGG	80176
rs551909677	snp	C/T	0.00676609	0.0577691	intron-variant	SPSB1	GRCh38.p7	1:9336593	TGGGGGATCCTCTGC[C/T]CGCGTGCGTTCAAGG	80176
rs551927913	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9304977	TGCTGCTTGGGTGCC[A/G]TTGCCCCATCCTGGC	80176
rs551940870	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9316807	GAGCCCAGCTTGGGA[A/G]GTGGCTGGCTTTCCA	80176
rs551945426	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9313403	GAAACACCGCTCTTC[A/G]TTTTCTATAAAATGA	80176
rs551976282	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9340590	CTGTGGAAACTCCAC[A/G]CCTGGCGGGAAGATG	80176
rs551980480	in-del	-/TA	0.00438332	0.0466095	intron-variant	SPSB1	GRCh38.p7	1:9334750	TCAACTTTCTGTCTC[-/TA]TGGATCCGATTGTCT	80176
rs551983999	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9313995	AGCCTGGCCAACATG[A/G]TGAAATCCCTTTTCC	80176
rs552084656	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9353330	CTCTCTCCCCCTTCC[C/T]TCCCGCAGCTTGAGG	80176
rs552112787	snp	A/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9360484	GGACAGCTGAAAACA[A/G]CAGAAGCGCTCAGGA	80176
rs552122461	in-del	-/C			intron-variant	SPSB1	GRCh38.p7	1:9355075	GGGTCGGGGGATGAG[-/C]CCCCCTTGCTGTCTG	80176
rs552130868	in-del	-/TC	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9294163	CTCTGCAAGTTTGTG[-/TC]TCTGAGTGTCTGTCT	80176
rs552137781	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9360033	GTGTTAAATTTGAGA[C/T]GCTTCTTCGACACAT	80176
rs552144079	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9348031	CTCACTGCAACCTCC[A/G]CCTCCTGGGTTCAAG	80176
rs552207112	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9313755	CCTGGCCAGTCCAGC[C/T]TGCCCGCTGTGCTTC	80176
rs552233177	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9351425	GTGGAAATGCAATAA[C/T]GCCAGCCCTCTCTGG	80176
rs552261443	snp	A/G	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9351973	CTGCCTGCCCTGCCC[A/G]GGGAAAACGCCCCAC	80176
rs552281664	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9336641	GCAGGGGCAGGAGGC[C/T]GCTGCCTGAGTTCAC	80176
rs552285988	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9353192	AGAGCCGCCTCAGCC[C/T]GCCCGGCCCCTCGAG	80176
rs552295190	snp	C/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9340446	ATGAAAACGTGGGTC[C/G]CAGAGGTTTGTTTTG	80176
rs552372473	snp	C/T	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9350560	CTCTCACTGTGTAGG[C/T]ACACAGTGTACACGT	80176
rs552383871	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9357471	TTGCCAGCATATCAT[C/T]GAGCTGGGGTTTGTA	80176
rs552407199	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9349660	GTGCCACACACAATC[C/T]GCCACCAGCATCGAC	80176
rs552419323	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9318654	GACCAAAGCCAGACC[A/G]TGTGGCTGGTGCCTC	80176
rs552487214	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9329916	TTTGGAATCTTTTCT[A/G]GGACTGATTCCTAGA	80176
rs552494328	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9367743	TGGGACAAGGACCGA[A/T]TCCAACACAGGCTCC	80176
rs552494418	snp	C/G	0.000399281	0.0141238	utr-variant-5-prime	SPSB1	GRCh38.p7	1:9355785	GAGGTCTCCTGGCAG[C/G]CCTCATTAGGAATTC	80176
rs552540454	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9324217	TCTGACGCAGCTGGA[A/G]TGGGCCTAGGTGGGA	80176
rs552566755	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291741	GTGATCTTTTAAATG[A/G]GAAGCACCCCTAAGC	80176
rs552574221	snp	C/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9299987	AAAAAAAAAAAGGGT[C/G]TCATGCTGGTCCATT	80176
rs552590701	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9362065	AGGGAAGGTCAGCTC[A/G]TCTCCTCAAGATCAG	80176
rs552633459	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9309765	GAGAATCGCTTGAAC[C/G]CAGGAGGCAGAGTTT	80176
rs552656356	snp	G/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9314853	AGGAGGCACAAATGA[G/T]GGAGGCAGCCAGTGG	80176
rs552675821	snp	C/G	0.00478085	0.0486577	intron-variant	SPSB1	GRCh38.p7	1:9329406	GAGGTGACACCCGGT[C/G]GTGGGTAGGTCAGGT	80176
rs552705969	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9357038	GGATGAGTGGATGAA[A/C]AAGTGGATGGATGAA	80176
rs552761840	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9320772	GGTGCCTGGAGGGTG[A/G]CTCCGTGTTTCTTGT	80176
rs552767045	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9328900	AGACGCCACCCCAAC[C/T]TGTGAGCCCCACATG	80176
rs552846169	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9348619	ACCTGGAGGAGCCCA[C/T]GAAACTGGAGGGATT	80176
rs552880995	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9293785	GGCGTCCAGGTTCCG[G/T]TGAGGACGGGACGGC	80176
rs552919835	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9294564	ATGAACTACACAGTT[C/T]GGGGGTGAGTTGGCA	80176
rs552968560	snp	C/G	0.00478085	0.0486577	intron-variant	SPSB1	GRCh38.p7	1:9339766	CTTCTACAGGGTCTG[C/G]GCAAGGGGATCGGCA	80176
rs553016569	snp	C/T	0.0225045	0.103662	utr-variant-5-prime	SPSB1	GRCh38.p7	1:9293034	CCCGAGCCTCCTCGG[C/T]CTTGGAGAGCAGCGG	80176
rs553026981	snp	G/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9341582	TGGTTGGGTCACTTC[G/T]GCCGGTGACATCTTG	80176
rs553031053	in-del	-/TGTC			utr-variant-3-prime	SPSB1	GRCh38.p7	1:9369063	ACATATATATATATT[-/TGTC]TGTAAGAATTATGTT	80176
rs553047932	snp	A/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9336792	ATTCGGTGATGAAAC[A/T]GCACTGCTCCCTGGA	80176
rs553088076	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9334872	ATAGCATGTATCAAA[A/C]TGTCCTTCCGTGTTA	80176
rs553090135	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9302578	GATGTCAGAACTCCA[C/G]GTTCTCTGGCCTTTG	80176
rs553128401	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9362109	GTGCCTCCTTCCTGC[A/C]CTCCACTCCAGCTGG	80176
rs553129905	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9368004	TACCAGGGGTACTAA[C/G]AGGTGCTTAGACAAG	80176
rs553160937	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9334695	AGCTCCTGGCACTGA[C/T]CCCCCATTCCTGCTC	80176
rs553253855	snp	G/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9345964	GGCCCCTTTGCCAGG[G/T]GCTCCATGGCCCAGC	80176
rs553288355	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9324424	GATGAGCGTGGGGGC[A/G]TCTGGTGCCTGGGTG	80176
rs553313101	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9313550	GGCACCTGATCTGGG[A/G]TGGGAGGATTCTGGG	80176
rs553378008	snp	A/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9294836	TGTCCCCCTCCTCAG[A/T]CCCCCCTCCCAGTGG	80176
rs553390202	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9351469	CTGAGTTTTAGGTAA[A/G]TGTGTGACAGACAAA	80176
rs553440885	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9332981	CCCATCCTGGGCTCC[A/G]TGGCTGAGACTTGGT	80176
rs553451001	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9300548	CCACAAATAACTTCA[C/T]TCCTTTTGAGAGACA	80176
rs553474070	snp	G/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9336384	GGCACGCACCACTAT[G/T]CCCGGCTAATTTTGT	80176
rs553478085	snp	C/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9302226	TGGTAAGGGGTGGAC[C/G]TGTGATGATTGATTT	80176
rs553514047	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9305734	CCACTTGTCATTCAT[C/G]CTTTTATTCAAACAT	80176
rs553515515	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9348852	AACCCCAACCCACCC[C/T]GTCCCATGGCTGCTC	80176
rs553653074	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9348289	TCTCGCTCCTGTCTC[A/G]GCGGTAGTGCTGTGT	80176
rs553684355	snp	C/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9339164	GTCCTGCCCTCACCC[C/G]TCTTCTGTCATTCTC	80176
rs553684376	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9351505	AGAAGCTTGGAGAAG[C/T]TCAGGGTGGATCTTG	80176
rs553743571	snp	A/T	0.00953873	0.0683987	intron-variant	SPSB1	GRCh38.p7	1:9333532	GACGGGGTTTCGCCA[A/T]GTTGGGCAGGCTGGT	80176
rs553771496	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9304548	GTTGGGATGGAAGCT[A/T]GTGGCATCTCCAAGG	80176
rs553787823	snp	A/C	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9307891	CCCCTCCCAGGCTTA[A/C]CCTGTGCCACTCCCT	80176
rs553851613	in-del	-/TG			intron-variant	SPSB1	GRCh38.p7	1:9324508	CGGCTCGGAGGGCTG[-/TG]GGCCCGGGACTCGGT	80176
rs553927330	in-del	-/C	0.00517822	0.0506191	intron-variant	SPSB1	GRCh38.p7	1:9340173	TCGCCCCTGTAGGAA[-/C]TGTTCTCAAGAGAGG	80176
rs553941543	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9300782	GCACAAGTAAGTGAC[A/G]TGAGGAAGTGGTCCA	80176
rs553990510	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9295980	CCTCAACACTAGATC[A/G]GTGAAATCCAGACTC	80176
rs553996715	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9321708	TGCCCTTGACTCCAG[A/G]ACCAGCCTGATGGCA	80176
rs554007843	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9311121	AAGTCCTTACCCCCA[C/T]GCCACTCTCAGGGGT	80176
rs554067752	snp	A/C	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9365877	TTCCATCTGCAGAAC[A/C]GCGTGGGCGGCCCCA	80176
rs554068638	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9316323	GCGTCCCTTGGCATG[C/T]TAGACTGTGCTAGGG	80176
rs554086740	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9342791	GCTGCCAAACCACAG[C/T]CCTGCACTTTTTCCT	80176
rs554097802	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9354953	AGGCATCCTAGCATC[A/G]GACTTTCCTCCCCAG	80176
rs554140477	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9335567	TAATCCCAGCACTTC[A/G]GGATTCCAAGGTGGG	80176
rs554156304	snp	C/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9321606	TAGGCAGCTCGCTAA[C/T]GCTGTGTTTCATCAC	80176
rs554171001	snp	A/C	0.00279162	0.0372561	intron-variant	SPSB1	GRCh38.p7	1:9344438	GTCTCGTGACGGGAC[A/C]GAGCAACTTGGGTCA	80176
rs554174645	snp	A/G	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9350035	TACACACATGAAGAC[A/G]CACCACACACATATA	80176
rs554202925	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9318247	AATGCAGCCGGCAGC[A/G]GAACAGTGACGGGTC	80176
rs554204362	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9310234	CAGAGTCTAGGGCCC[A/G]TGCTGGTGGGACTTG	80176
rs554229180	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9339233	TCTTTTCCCAGGCAC[C/T]TGCCTAGAATATTCG	80176
rs554229500	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9355313	GCTACCTGGGGCTCC[A/G]CTTCCCCTCTGAACC	80176
rs554246674	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9365371	GTCTTCTGTCCTTGG[C/T]CTCCCAAAGTGCTGG	80176
rs554255093	snp	C/G	0.0154538	0.0865337	intron-variant	SPSB1	GRCh38.p7	1:9293354	AGGGGGTCCCGGGGC[C/G]AGGCGCGGCGGGGGT	80176
rs554292149	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9339582	ACTCATGTGGTTCTT[A/G]AGGACTAGCAGGGCT	80176
rs554341428	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9326139	TCGGGTGGAATGTTC[G/T]TGGTGGGGCTGAATT	80176
rs554378250	in-del	-/GCGGGGC	0.00517822	0.0506191	intron-variant	SPSB1	GRCh38.p7	1:9323324	GGCCCCAGCCCCTTG[-/GCGGGGC]GCTCAGCAGTGGATG	80176
rs554395404	snp	A/G	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9328168	TAGAGCCAGACGAAC[A/G]TGGCTGTGTGGAGGA	80176
rs554432930	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9344905	CACTCCCAGAGGTGA[C/T]CTTTGCCAGCTGGCA	80176
rs554455734	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9343581	AAAGAAGTTTAAAAG[A/G]CAGGGAATTCATAAG	80176
rs554484188	snp	A/C/G/T	0.0119155	0.0763244	intron-variant	SPSB1	GRCh38.p7	1:9316559	TGGATGGCGAGGAGG[A/C/G/T]GGGGGCTGATCGAAG	80176
rs554509458	snp	C/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9334058	ATTTTTCAATTGTAG[C/T]AAATACATATAACAT	80176
rs554524768	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9311581	CAGACTTGAACCAAC[A/G]CTTGAGCCAGAGCAG	80176
rs554530633	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9327391	CCAGGCAAGCGCATA[A/G]CTAAAACAGGATAGT	80176
rs554576505	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9304230	CCGGGGTCTTTGGCC[C/T]GGGGCTGAGAATGAC	80176
rs554674182	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9302710	GTAGAGTCTTTTGAA[A/G]TTGCAATTACAATGC	80176
rs554701701	snp	C/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9354152	TGGCCCTGGCTGGCC[C/G]CATACTGAAGGGGGA	80176
rs554712895	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9303294	ACCCTTCAGGAATGA[A/G]TGTTTGGGTCACTCT	80176
rs554783858	snp	C/T	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9307387	AACCCCATCCACATT[C/T]GGCGTCACCTCCCAT	80176
rs554797046	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9361046	TGGCTTTGCCTTCCA[A/G]TACAACTAAAGAAGG	80176
rs554824510	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9300557	ACTTCATTCCTTTTG[A/G]GAGACAGCTCTTGGC	80176
rs554847016	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9354874	GTGAGATCTCTCCCC[A/C]AACCCAGAGTCCCTG	80176
rs554864570	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9355396	GTCATGGCTGAGTCC[C/T]GGTTCTGTGGCACCA	80176
rs554882301	snp	A/G	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9313119	AAAAAAGTCAAGTCC[A/G]GGCGCGGTGGCTCAT	80176
rs554898696	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9349678	CACCAGCATCGACTC[C/T]TCGATCCAGATGAGA	80176
rs554943794	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9308375	GGCCCCCGGAGCCAC[A/G]GTGCCCTGACTGTGG	80176
rs554977059	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9340232	CTCCTGTCTGGTTTT[C/T]CATTTGGGGGCCTAG	80176
rs555036480	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9330430	AGATTGTGTCACTGC[A/G]CTCCAGCCTGGGCGA	80176
rs555045590	snp	A/C	0.00438332	0.0466095	intron-variant	SPSB1	GRCh38.p7	1:9350116	TACACACACACACAC[A/C]CCCCTACCACCCGCA	80176
rs555056421	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9345011	GATCCCCTATGTCCA[A/G]GAGACTGCCTTGTTG	80176
rs555071144	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9328199	TTCAGTACAGGGGCT[A/G]AGGGAGGAGGCAGGG	80176
rs555129194	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9316318	TGGGGGCGTCCCTTG[A/G]CATGCTAGACTGTGC	80176
rs555139462	in-del	-/A	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9314174	ATTGAGACTCTATCT[-/A]CAAAAAAAAAAAACA	80176
rs555168368	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9352838	TCCCACCCTCCCCTC[C/T]CTCCCCCAGCCTCCT	80176
rs555193918	snp	C/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9323594	CGTGGAATCCAGATG[C/T]AAACAAAGCGGAGAA	80176
rs555194129	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9362958	CCCCAGGCCACAGTG[A/C]AGGTGCCCACCCCCT	80176
rs555231785	in-del	-/GA			intron-variant	SPSB1	GRCh38.p7	1:9359850	AGGATGGAAGCCGGG[-/GA]GGGGTGGGTGGCGGG	80176
rs555255437	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9363632	CTGGGGCTGGGGCTG[C/T]GGTGTCAGCCACTCA	80176
rs555334642	snp	A/G	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9323095	CCCTCCCCAGCTCCG[A/G]CCTTCGAGGACTTTG	80176
rs555513312	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9354217	TCTGGGAGCCTGCAG[A/C]CTCCCCTACCCCGGG	80176
rs555573178	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9352320	CCTCTGGGGATCCCC[C/T]GCTCCCCACCATCCG	80176
rs555592072	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9325669	TCCAGCCCCTGTGTT[C/T]TCACAGGGGACGGGT	80176
rs555614649	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9306587	GATGAGAAAAACTAG[C/G]GCAACTCTGGGCCTC	80176
rs555653466	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9301791	TAGTCTGCCAGAAGC[A/G]GAGACTAACACTGAG	80176
rs555658207	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9369226	TTTTTCGGGGCAGGG[A/G]ACCTTACCTGTAAGA	80176
rs555727391	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9296760	ATGCGGGGCAAGAGT[C/G]GGGAGATGTACGTCC	80176
rs555745900	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9305266	TTCACTTTCCAAAAC[C/T]GGATCCCCTCACTCC	80176
rs555784779	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9369335	TGGCCTTGACCCAGC[C/T]GTCCTCACAGATGCC	80176
rs555817733	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9316776	TGGGTCTGGGTCTGG[A/G]GGCCGCAGCAGCTTC	80176
rs555842219	in-del	-/CT	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9330704	GCATGTTCTTCTGAA[-/CT]TTTTTTTTTTTAATC	80176
rs555850808	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9359109	AGAGCATCACAGCCG[A/G]GCGCTATTAGTCAGT	80176
rs555858263	snp	C/T	0.00438332	0.0466095	intron-variant	SPSB1	GRCh38.p7	1:9326780	TGCTTCTGAGGGGCC[C/T]TCCTCATTCCTGCAG	80176
rs555912128	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9359559	ATGCAAAAATTAGCC[A/G]GGCGTGGTGGCATGC	80176
rs555916817	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9301891	TTGGAAGGGGCAGCG[C/T]TTTGTCCTTACTGGA	80176
rs555964612	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	SPSB1	GRCh38.p7	1:9369908	GTGAGCCATTGTGGG[C/T]GTCCTCAGAGTCCAG	80176
rs555980099	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9348237	GGCGTGAGCCACCGC[A/G]GCAACTTTTTTTAAC	80176
rs555997443	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9358347	GTCTGTGCAGCCTGG[C/G]GCCCCCAGGTCATGG	80176
rs556056421	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9358934	GTCCTGTGAATAGGC[A/G]ATTTCCTGCTTAGTT	80176
rs556074466	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9295755	AACTTGCCTGCAGAC[A/G]CATTTTCAAATTCAG	80176
rs556093683	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9343388	TCTGGCTTCCTTCAC[A/G]TTAATATAAAGTTTT	80176
rs556111029	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9313951	GAGGCCTAGGCGGGC[A/G]GATCACTTGAGGTCA	80176
rs556152856	snp	C/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9307047	ATTCTCCCTCCTTAG[C/T]CTCCTGGGTAGCTGG	80176
rs556154317	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9312392	TTGTAGGCAGTGAGC[A/G]CTAACACAGGGTTCT	80176
rs556169617	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9338170	ACCTGGAGACATGGA[A/G]GTTGGCGGTTGGGGG	80176
rs556201297	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9317773	CAGGCGTGAGTCACC[C/G]TGCCTGGCCAGAAAA	80176
rs556247213	snp	C/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9311089	CCGCCTCTAGCCTCC[C/G]AGGCTCCCTGAAAGC	80176
rs556307042	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9300441	GGTTGAGGTCAGCGG[C/T]AGACAGGGAGGCTGC	80176
rs556356041	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9347829	GGACAGGGACTGCCT[C/T]GTTGTACCTGCACAC	80176
rs556373055	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9316375	GGGGCACAAGGGAGG[A/G]GCATGTGTGCACGTG	80176
rs556386676	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9312322	ACGAGCCATTGTGTC[C/T]GGTCTGTCTGGTTTT	80176
rs556398321	snp	C/G	0.000399281	0.0141238	downstream-variant-500B	SPSB1	GRCh38.p7	1:9369983	TGGGGCTGAGTGCAC[C/G]GTGATGTTTGCTGAA	80176
rs556404198	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9296850	AACAGCACATTGGGG[A/G]ATCTGTCCTGCTGCC	80176
rs556410079	snp	A/G	0.00318978	0.0398085	intron-variant	SPSB1	GRCh38.p7	1:9316592	GGTTCAGGGGCTGCC[A/G]TTTACGAAAGGCTGG	80176
rs556441991	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9297540	GACACCAAGGGAGCA[C/T]GTGTGGGAGTGGATA	80176
rs556443099	snp	G/T	0.00478085	0.0486577	intron-variant	SPSB1	GRCh38.p7	1:9326830	ATCGGAAAGGCTTAT[G/T]GCCTCTGAGTCAAAA	80176
rs556466469	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9351280	GATCTGCCCTAGCCC[A/G]GACTTCCAAGTCCTT	80176
rs556497908	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9328107	AGCCCCTTACCTCAC[A/G]CAGTAAACATCTCAG	80176
rs556512506	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9359693	GGCAACAGAGCAAGA[C/T]TCCGTCTCTGGGAAA	80176
rs556534218	snp	C/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9319850	GTGGCCACTGGAGCT[C/G]CTGGCCCAGCCAGTC	80176
rs556556715	snp	A/C	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9314970	AGTCCTTGGCACTGT[A/C]GTATTCCTTTTGAAG	80176
rs556625012	snp	A/G/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9294735	TTTTCTCGTTGGGGG[A/G/T]GCTGGGCCCACAACT	80176
rs556680856	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9353505	TCACAGAACTCTCTG[A/G]AACCAGGGCGGCCCT	80176
rs556699877	snp	C/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9354911	CTCCTGAAGGACCCA[C/G]GGGATGGTGAGGCCA	80176
rs556710583	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9354641	AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT	80176
rs556735149	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9362424	ACTGCGTAGTGTAGA[G/T]GAAAACACACACACA	80176
rs556740198	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9327345	CATGGATATGTATGT[C/T]TTTGGCAGATACATG	80176
rs556809113	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9304661	AGTTTGGGGGTCATC[A/G]TGAATAATGACCTAC	80176
rs556881491	snp	A/C	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9332373	CTAATGTGGGAAGCC[A/C]AGAAGAGGAGGAATT	80176
rs556916978	snp	A/G	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9367283	TGGGCTCCTGGTGGC[A/G]GCTATTCACATGCTA	80176
rs556944431	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9308119	CAAGTTACTGTCTTA[A/G]TTCCATTCCTTCCAG	80176
rs556945094	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9332900	GTGCGTAGAGGGTGA[C/T]GGAGACCACAGGAAG	80176
rs557030291	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9351544	AGCTACTGTCTCGGC[A/G]CATGAGCTTGGAAGC	80176
rs557052377	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9356743	TTTGCATCGGGTTAA[A/G]TGAGGAATTCTACCC	80176
rs557072144	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9328300	CTCATGATGTTGTGC[A/G]AAGATGCACTCCAGG	80176
rs557114028	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9357192	ATGGATGAGTGGATG[A/G]ATGGATGGGTGGATG	80176
rs557118972	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9363651	GTCAGCCACTCAAAA[G/T]AAGGCACTGGATGGA	80176
rs557141569	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9324262	ACTACCACGTGGAGC[C/T]GGCACATAGTGGGAC	80176
rs557198475	snp	C/T			utr-variant-3-prime	SPSB1	GRCh38.p7	1:9367838	CTTTGAAAAAAGACA[C/T]AGAGAATAAACTCCT	80176
rs557236570	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9362190	ACCCACCCTCCCTCC[C/T]TCCCTTCCTTCCTTC	80176
rs557240106	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9341637	TTCCTCTTGGGAGAG[A/G]TGTTTTCTAGCAGTT	80176
rs557279592	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9340661	TCTGCGGTCTGAGCC[A/G]CCTGTGCTGTGATGT	80176
rs557282981	snp	A/C	0.00636936	0.0560724	intron-variant	SPSB1	GRCh38.p7	1:9325240	ACCCCCCCCCCCCGC[A/C]CCGCCTCCACCGGTG	80176
rs557336971	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9335488	GCCTGGGTGACAGAG[C/T]GAGTCTCTGTCTCAA	80176
rs557448174	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9362972	GCAGGTGCCCACCCC[C/T]TCGGTAGATTTCAGC	80176
rs557493779	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9295644	GCTGGGGAATGGGGT[C/G]GGGGCCTAGCCCGTG	80176
rs557499826	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9301360	AAAAAATTAGCTGGG[C/T]GTGGTAGCTCATGCC	80176
rs557521970	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9305351	ACCCTGTCACCCAGA[C/T]ACATGCACCCTCAGC	80176
rs557559632	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9357761	ACCGTGCTGGTGTGG[A/G]AGGTGAAGGCTCCAT	80176
rs557636719	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9294774	CATCGTGGGGTGTGA[A/G]GAGAACAGCAAGCAA	80176
rs557651211	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9367839	TTTGAAAAAAGACAC[A/G]GAGAATAAACTCCTA	80176
rs557683241	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9352236	ACCTGGACAGACAGA[C/T]AGTGGATGTCCCACG	80176
rs557702669	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9362898	AGAAATTATTTAAAT[G/T]AATGAGCGCCTAAGC	80176
rs557746767	snp	G/T			synonymous-codon	SPSB1	GRCh38.p7	1:9356026	ACTGGACATGCCCCC[G/T]GTGTCCTATGATGTC	80176
rs557749582	snp	C/T	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9316227	CTGACCCTGGGGCTC[C/T]GGCACCCCCAGGAGA	80176
rs557779563	in-del	-/AATAATTAAAACAGAAA	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9298280	AAAAAGTCTAACTTG[-/AATAATTAAAACAGAAA]AATAATTAAAACAGA	80176
rs557851840	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9335706	TTGGGAGGCTGAGGC[A/G]GGAAGATCACTTGAG	80176
rs557855520	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9325897	GGCAGAGGACTTGGG[A/C]AGTACAGAGATCCTG	80176
rs557857804	snp	C/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9332166	GAATAGCCTGGGCAA[C/T]ATAGTGAGACCCCAC	80176
rs557866965	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9321352	GAGCTCTAGACAGCC[C/T]GATGGCAGGGGGTGG	80176
rs557877760	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9351644	GGGGACCCGCAGAAA[A/G]GGTGGATCTGTGCGG	80176
rs557891729	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9352268	CAAGGTGAAGCCGTC[C/T]TTTCTGGTGGCTCTT	80176
rs557921154	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9306280	CTGCAGCAGTCGGCT[C/T]TTCTGCTCTGTGGTT	80176
rs557923312	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9324826	CTGGGCCAGACAGTC[A/G]TGTTTGCGACAAGTC	80176
rs557939223	snp	A/G	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9296110	CCGGCTCTGTGCTAC[A/G]GAGTGCTTTATGGAC	80176
rs557958261	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9364323	AGAAGACCTACTCCC[A/G]ACAGCCAGGCCAGAC	80176
rs558008172	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9325183	GGCATCCAAGAAGAC[C/T]TGTACTCCGCCCTCC	80176
rs558095660	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9302448	GAGTCACTCAACTGG[A/G]TGGGGAGGATCTGCC	80176
rs558111058	snp	A/C	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9330238	TTTGGGAGACTGAGG[A/C]GGGCGGATCACCTGA	80176
rs558150436	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9295667	AGCCCGTGGAAGCCA[G/T]CGCTGCCCTCCCACC	80176
rs558185138	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9293743	CCGCGGATGGGTCAC[C/T]GTCCCCGGGCGTGTA	80176
rs558196361	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9301758	AAAGCCGACCTGGCT[A/G]TGGCTACCACTGGCT	80176
rs558210102	snp	A/G	0.00358779	0.0422022	intron-variant	SPSB1	GRCh38.p7	1:9342544	AGTGAGAAAGTAGGC[A/G]CCTAGGAATCCAAAC	80176
rs558215673	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9334147	CTGGAGTGCGGTGGT[G/T]CGATCTCGGCTCGTT	80176
rs558230415	snp	A/G	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9323152	TTCCTTCCTGCTGCC[A/G]TGTTGGAGGGGGGTA	80176
rs558237332	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9296639	ACACATACACACACA[C/T]GCTGGATTATTTTGA	80176
rs558243918	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9363742	TCTCATTCTGTCACC[C/T]AGGCTGTAGTGCAGT	80176
rs558245844	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9369200	ACCCCCTTATTATTT[C/T]GACGGTTTTTTTTTT	80176
rs558279077	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9334801	CAATCATATAGTATT[C/T]GTCTTTTTGTTACTG	80176
rs558322961	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9304924	GCAATCCTCCCAAAG[C/T]GCTAGGATTATGGGC	80176
rs558360962	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9310412	AAGAAGACCTAAAGG[G/T]CCGGGCACAGTAGCT	80176
rs558417992	snp	G/T	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9294731	AGAATTTTCTCGTTG[G/T]GGGGGCTGGGCCCAC	80176
rs558437021	snp	C/T	0.00199481	0.0315187	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9368591	TTGATGTGGGTTTGA[C/T]TTTGCTTTTGCTTTT	80176
rs558465291	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9302887	CACTGCGCATCATAT[C/T]CCCTAGGGACCCGCT	80176
rs558501947	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9327786	CTACTCGACTCTGTA[A/G]CGTGAAAGCAGCCAC	80176
rs558523088	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9307490	TAAATGGAACCATAC[A/G]TTGCATGGCCTTCTG	80176
rs558548779	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9323667	CACACATGGCTGCCC[A/G]CGCGTCTCCAGGCAC	80176
rs558576369	snp	C/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9366996	GGCTCCCATGTGTTC[C/T]GACCGACAGGCCCCA	80176
rs558585442	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9339356	CAGCTAGGACTTAGG[G/T]CTGTGACTCACCGCC	80176
rs558606949	snp	A/C	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9310928	AATATATAAATTATA[A/C]GTACATGTCAGGGTT	80176
rs558609544	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9347213	GATCCTTAACACGTA[A/C]CTTCATGGATAAAGC	80176
rs558622452	snp	A/C	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9350970	TGGTCCAGTGTTAAC[A/C]GGAGCCATCCAGGCA	80176
rs558633709	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9341409	GTTGCCTGCCTCCCC[C/G]CACTAGACTGAGCTC	80176
rs558641390	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9366340	AGCCTCACTGTCAGA[C/T]AGAAGCACAGACACC	80176
rs558654587	snp	A/G	0.00557542	0.0525036	intron-variant	SPSB1	GRCh38.p7	1:9299079	AGACAGATGGACTTT[A/G]GAAACTGATAGTGGA	80176
rs558667756	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9346496	TTCCTTCAACAGACC[C/T]CTTCCTAAAACACCA	80176
rs558685798	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9349134	TCACTGTGTTGTAGG[A/G]AAGGCAGAATCTCCT	80176
rs558688956	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9346585	TTTGGGGGAAGGTGG[G/T]GTCTGCAGGGTTGTG	80176
rs558696561	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9336320	GCAACCTCTGCCTCC[A/G]AGTTCAAGTGATTCT	80176
rs558708569	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9307869	GTGGTCTTCGGGGTG[C/T]GCGTGGCCCCTCCCA	80176
rs558745482	snp	A/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9303339	CACAGCCAGCTGAGG[A/T]GCTTGTTGCAGACGA	80176
rs558821925	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9344360	CCACTTTGAGAACCA[C/T]TCCTGTAAAACAGGG	80176
rs558850959	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9345051	GGCAGACTTTGGATG[C/T]ACTCCAGCCTCTTCC	80176
rs558885814	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9349564	AAGGCGTGCAGGAGC[A/G]TGGGTGGGTGGACGG	80176
rs558898696	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9304768	GGCAACTGGGCTCAA[C/T]GCTCAAGCAATCCTC	80176
rs558935481	snp	A/C	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9299779	CCACTGCGCCCGGGC[A/C]GACATCATCTCTATA	80176
rs558988814	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9345886	GGGTCCCTCCTCAAG[C/T]TGGCAGTTGGCAGGG	80176
rs559051107	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9340769	CTGCTGTTTTTTATT[C/T]TATGGAAAGTCCAGC	80176
rs559078204	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9322885	CCCCACCCGCCCGGA[C/T]GCTCTTCTCAGCCCC	80176
rs559078246	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9328415	TTTAAGATGCTGATG[C/T]GTTTGTGACTCTCTA	80176
rs559121315	snp	C/T	0.00517822	0.0506191	intron-variant	SPSB1	GRCh38.p7	1:9350394	AGAGGAGGAGGCAGG[C/T]GCGGTCCTGGGGACG	80176
rs559138170	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9323210	GCCTTTTCGCTCTCA[C/T]GAAGTGCCCTGGCTG	80176
rs559208946	snp	A/C	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9314175	ATTGAGACTCTATCT[A/C]AAAAAAAAAAAACAA	80176
rs559284646	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9313314	CTGAGGCAGGAAAAT[C/T]GCTTGGACCCGGGAG	80176
rs559335318	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9296983	GACCACATCAACAAC[A/G]GGCTTAGGCTCTCGG	80176
rs559371579	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9354914	CTGAAGGACCCAGGG[G/T]ATGGTGAGGCCAGAG	80176
rs559386476	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9367012	GACCGACAGGCCCCA[A/G]TGGCAGCTGCTTGCC	80176
rs559398767	snp	A/G	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9299123	AACCAAGTGGTGACT[A/G]CAAAATTCACACATC	80176
rs559431408	snp	C/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9334175	GTTGCAACTTCCGCC[C/T]CCCGGGCTCAAGCAA	80176
rs559456891	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9337920	TAACTTAAGAGAGTG[A/G]CCTGGTGGCTCTTCC	80176
rs559486055	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9340827	AGCCTGTCTGATGTC[A/G]CGGAGCAGCTCTGCC	80176
rs559525092	snp	C/T	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9366598	TTTTTTTTTTTGGAC[C/T]GAGTCTTGCTCTGTC	80176
rs559564041	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9366034	TTTCAGACTCCTGAG[A/C]TCTGAAGCTGACGGC	80176
rs559565355	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9360776	ATAATGAAGTACATC[C/T]GCAAGGCCCTGTTTC	80176
rs559571605	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9335670	CTGAGCATGGTGGTG[A/C]ATTCCTGTAGTCCCA	80176
rs559576870	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9333842	CTTTCCTCTCCAGCG[C/T]GGCTCCGGGGAAAAC	80176
rs559577588	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9340322	GTTTGGGGACTGGCC[A/G]GAGCCCCGCGGTCTG	80176
rs559598884	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9294358	TCTGTGTGTCTTTGT[A/G]TGTGTTTCTCTGTGA	80176
rs559605376	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291700	GTGGGGATTAAGGGC[A/G]TGAGAGCCACCACCT	80176
rs559617421	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9345300	CCTGTTGGTGGCTCT[C/T]TTCTTGGAGATGGCC	80176
rs559625538	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9361251	TAAGTGGTCCTCCTG[C/T]CTCGGTCTTCCAAAG	80176
rs559629793	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9318578	CTCAGCCTCTTTGAG[C/G]CTTGGTTTCCACATC	80176
rs559746038	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9356855	TGAATGATTGGTTGG[A/G]TGGATGGATGATGAA	80176
rs559778638	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9363992	GGCATAAGCCACCGC[C/G]TCCAGCCTAGAAACA	80176
rs559780616	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9369466	CAGTTTTGAAACTCC[C/T]GTTCTATTTTATGAT	80176
rs559792471	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9302812	TCCAATATATGGTGC[C/T]GGTTTCTCCCGTAGC	80176
rs559803680	snp	G/T	0.00597247	0.0543191	intron-variant	SPSB1	GRCh38.p7	1:9324921	AAAAGCGAGTGGGGT[G/T]GGGGAGCAGGGACAC	80176
rs559909267	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9321539	GGATTCAGCTCAGAA[C/T]GGGGAAGAGGGTGTT	80176
rs559918873	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9368780	GCGCGGGTCTCTGCT[C/T]AGCACCCCAGCCGGG	80176
rs559929951	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9359310	CAACTCCGCTGCAGC[A/G]TGGTGATAGGGTGAG	80176
rs559962677	snp	A/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9296430	GAAGCATGGGCTCAT[A/T]TTTTTAGTGAAATTT	80176
rs560002475	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9347930	CCCCACCTTCTTTGC[A/C]GTTTCCCTGCAACTT	80176
rs560034444	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9359697	ACAGAGCAAGACTCC[A/G]TCTCTGGGAAAAAAA	80176
rs560057532	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9337670	CCGCTCAGAGCCTCA[A/G]GCCACCCTCCTGATG	80176
rs560079566	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9368855	CAGAGCCTCAAGAGG[G/T]GTAGCTCGGCTGCCG	80176
rs560111346	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9307587	TTCCCGTCCTGGCTC[A/G]GTTGTAGAGGCCACG	80176
rs560124899	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9301602	GACATGAGGTATGTG[A/G]GTAGGATGACCTAGG	80176
rs560165646	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9301914	TTACTGGAGCAGGCA[C/G]TTATTCTGGATACAG	80176
rs560173967	snp	A/T	0.00597247	0.0543191	intron-variant	SPSB1	GRCh38.p7	1:9338213	TCTCCCCTACCCCGT[A/T]TCTTCAGGCTTCTGC	80176
rs560174661	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9307208	GCTGGGATTACAGGC[A/G]TGAGCCACTGTGCCT	80176
rs560202523	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9296997	CAGGCTTAGGCTCTC[A/G]GGGCCTTTCTTGGAG	80176
rs560203826	snp	G/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9327031	GGGGGTCTTGGCTTA[G/T]GGGCAGGTGCTCAGG	80176
rs560236715	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9332487	TTTGAGTCTACAAGG[A/G]ATGTATGAGTGGGAG	80176
rs560286676	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9302494	CACCATCCAGTCAGC[C/T]GGGGGCCTGGAAGAA	80176
rs560347440	snp	G/T	0.0154538	0.0865337	intron-variant	SPSB1	GRCh38.p7	1:9299532	TTGCCTAGGCTGGAG[G/T]GCAATGGTGCAATCT	80176
rs560384043	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9316798	AGCAGCTTCGAGCCC[A/G]GCTTGGGAGGTGGCT	80176
rs560385154	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9338903	CCACAGAACAGGAGC[G/T]TGGACACCCTGGCCC	80176
rs560385583	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9342423	CAGTCAGGCCCCAGC[A/G]TCAACCGTGGGAGAG	80176
rs560388110	snp	A/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9358030	GGCAGAGGGGGGTGA[A/G]GCCCCCCACCAGAGG	80176
rs560418761	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9315302	AAGGGACACAGCCCC[G/T]TGCCAGTGTTGCCCA	80176
rs560449655	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9333573	TGACCTCAGGTGATC[C/G]GCCCACCTCGGCCTC	80176
rs560527631	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9359949	AGCAAGGTGACTTGC[A/C]TTGTTTGGGTTGAGC	80176
rs560571500	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9344030	CCTGACCTTGTGATC[C/T]GCCCACCTCGGCCTC	80176
rs560585027	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9353915	AAGAGCAAAACTCCA[C/T]CTCAAAAAAAAAAAA	80176
rs560591432	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9360514	AGGCCAGGTGTCTGC[A/G]ATCAGGATGGTAGCG	80176
rs560595606	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9354507	ACTTCTCTCTTGAAC[A/G]AGGCTCAAATCTTCT	80176
rs560692905	snp	A/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9348967	TGTGTGTGTGTGTAT[A/T]TGTGCGTGTGTGCAC	80176
rs560754549	snp	A/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9364601	GGGATCCTTGACCTT[A/T]AAGAACCCAAGGTTA	80176
rs560759266	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9311729	TCTGCCGGGGGTTGC[C/T]GAGTGGTAGACGTGA	80176
rs560781214	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9307085	GGCACGTGCCACCAC[A/G]CCTGGCTAATTTTTG	80176
rs560785401	snp	C/T			upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291386	AGTGACGGGTTTCAT[C/T]GTGTTAGCCAGGATG	80176
rs560799640	snp	A/G	0.00279162	0.0372561	intron-variant	SPSB1	GRCh38.p7	1:9359874	TGGCGGGGGCGGCCC[A/G]GTTCCGGGACTCTTT	80176
rs560803723	snp	A/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9326625	GGGGGACCAGAGGCC[A/T]TGCTGAGGCTCCTGT	80176
rs560820944	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9322144	TTAGCTCCTGGTGGT[C/T]GAGGCTGGCTCCGTC	80176
rs560860011	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9338333	CCCAGGGAGGAGGTT[C/T]GTGACTGTATGGGGG	80176
rs560888831	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9332539	GATATTTGGTGGACA[C/T]GTCAGGTTCACAGGC	80176
rs560937681	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9303710	GGATAGTAGTGTCAC[A/G]ATAGGTGGAACTATG	80176
rs560938529	snp	C/T	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9297740	TTTCTGGGTCTCCTT[C/T]GGTTTAATGTAGAGT	80176
rs560960532	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9297241	TCTGCCACCCTTGGG[C/T]GTCTCTTGGAAAACT	80176
rs560996600	snp	C/T	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9305665	CTTCCTTCCATGCCC[C/T]GTGGGAGGTCAGGAA	80176
rs561016975	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9341682	TTCTCCCTTCCTGAA[C/T]GGTGACCACGCTGGC	80176
rs561020674	snp	C/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9333095	AGAATCAGCCTCCCA[C/G]GTGCACACTCCATGG	80176
rs561083982	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9354075	GGCCGCCCCGGGAAC[A/G]GGGTCTCGTGGGGCC	80176
rs561125816	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9306804	GTCCTAGGTAATGGG[A/G]ATTGGTGTCTGAGCT	80176
rs561179804	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9307951	CCAGAGGTGCCCCAT[A/G]GGGACCGACCCTGAG	80176
rs561204667	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9355019	TTCTAGTTGAAGGGT[A/G]TGGGCAGGAAAAAGG	80176
rs561323922	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9329307	GGGTGGACAGGTGGA[C/T]AGGCGGATGGGTGGA	80176
rs561341248	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9305997	TGCAATTGCGAGTAA[A/C]GTGGGAGAGGGGTTC	80176
rs561362547	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9339412	GTCCTCAGGTAATTC[C/T]GGGGCGAGTCTGGAG	80176
rs561367416	snp	C/G			upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291402	GTGTTAGCCAGGATG[C/G]TCTCCATCTCCTGAC	80176
rs561374784	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9339828	TGGACCTGGTGGCAG[A/G]ACAGGGGAAGCTGCC	80176
rs561375049	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9327126	AGCACAACCCCCAGT[A/G]CCCACTTGCAGCGCT	80176
rs561406278	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9305506	TCTTGGACACCTGTC[A/G]GATGAAGGAGTAGGT	80176
rs561497448	snp	C/G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9336987	GGCCTGACTCCCTAT[C/G/T]GTGGCATTCAAGGCC	80176
rs561561881	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9344068	GCTGGGATTACAGGC[A/G]TGAGCCACCGCACCT	80176
rs561564674	snp	A/G/T			intron-variant	SPSB1	GRCh38.p7	1:9301328	AGACTCCCCGCCCCC[A/G/T]CCATCTCTACAAAAA	80176
rs561739769	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9318447	CCACGAAGCCCCCCT[C/G]CCATGTTCCTCTTTG	80176
rs561764181	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9347222	CACGTACCTTCATGG[A/G]TAAAGCATTCAGGAC	80176
rs561766120	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9341806	CTCCCGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG	80176
rs561776437	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9336436	TCTCCACGTTGGTCA[A/G]GCTGGTCTCAAACTC	80176
rs561780824	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9329208	TCAGTCTGCATGGGG[C/T]CCGAGCACAGCCGGT	80176
rs561795344	snp	A/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9357366	TGATGGATAAATGGA[A/T]AGATGGATGAATTAA	80176
rs561822471	in-del	-/A			intron-variant	SPSB1	GRCh38.p7	1:9312462	CAGTTCGCCTATTGT[-/A]AATGTACACATTGAT	80176
rs561901959	snp	C/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9346689	GTCTGCTCTCAGTGC[C/T]TCATTCCTCCTCACC	80176
rs561903571	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9320723	CCCGGGCTCGCCTCT[C/G]TCGGCTCTGGCTGGC	80176
rs561976927	in-del	-/C	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9323311	TGGGCCCCTCTCTGG[-/C]CCCAGCCCCTTGGCG	80176
rs561999743	snp	A/G	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9353188	CTCGAGAGCCGCCTC[A/G]GCCCGCCCGGCCCCT	80176
rs562062037	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9347993	TCTGACGCCCAGGTT[C/T]GAGTGCAGTGGTGCG	80176
rs562085449	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9316531	CTGGGCCAGGCATCA[C/T]GCCTTGAGGTGCTGG	80176
rs562126839	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9368648	TCAGAAGCTCTGGGT[A/G]TGCCAGAGGACCCCC	80176
rs562133676	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9311217	ATTCCCTGAATGCCC[A/G]CTCTGTCCTGGCTGT	80176
rs562218537	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9295698	CCCATGGTGTGTGCC[A/G]TGCTCCCTTCCTGCA	80176
rs562246006	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9363807	CCAGGTTCAAGCAAT[C/T]CTCCTGCCTCAAACT	80176
rs562335653	snp	G/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9363243	GAGGCGTGACCTGTT[G/T]ATGTACTTGAGGACC	80176
rs562348763	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9361317	CGGATCTGTTTTCTT[A/G]GTGGCAGACCTGATC	80176
rs562400757	snp	C/G	0.00358779	0.0422022	intron-variant	SPSB1	GRCh38.p7	1:9352363	TACAGCCCCACAAGG[C/G]TGTGTCTTAAGTGGA	80176
rs562450523	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9331631	TCACCGTGCCTAGCC[A/G]GCACTCATTCTTATG	80176
rs562456034	in-del	-/TG	0.362826	0.223092	intron-variant	SPSB1	GRCh38.p7	1:9294031	GACTCTAAGTGACTG[-/TG]TGTGTGTGTGTGTGT	80176
rs562519960	snp	C/G	0.00279162	0.0372561	intron-variant	SPSB1	GRCh38.p7	1:9311639	TATGGGGCAGGGGAG[C/G]ATTCTGTAGAAGATT	80176
rs562522620	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9310247	CCGTGCTGGTGGGAC[C/T]TGCCTCTTGGGTTGA	80176
rs562559280	snp	A/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9306079	TCAGCCAGCAGGCTG[A/T]GTCCCAGCCATGCTC	80176
rs562567243	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9337171	GGTCGTTTCCATCTG[A/G]TTGTCCTAGAAACGG	80176
rs562574208	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9368316	ATGTATGCCTCGCCC[A/G]CCCTCCCTGGGCACA	80176
rs562581262	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9337599	AGCTGTGAGTGCAGC[A/G]CCTCCAGCCTTGCTG	80176
rs562581337	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9331093	CCTTTCATATTCTGT[C/T]GTGCTCTCCCCGCTG	80176
rs562600619	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9342614	TGATCACCCTGACAT[C/T]GGTTCTCCCATGTCC	80176
rs562642030	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9310501	AGTTCCTGACCAGCC[G/T]GGGCAACATGGTGAA	80176
rs562660623	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9347444	TTCAATTCAAAAAGC[A/G]TTTTTTCCCTCCCAC	80176
rs562753715	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9302005	CCTTTCCCACTGTCA[C/T]GCTGTCCGTGTAGCA	80176
rs562840405	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9309702	ATAAAAATTAGTCGG[A/G]GATGGTGGTGCATGC	80176
rs562868388	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9343630	GCGACATTTTCATTT[A/C]TCCGGGCTCCTTTCT	80176
rs562914119	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9307158	GTCTCGAACTCCTGA[C/T]CTCAGGTGATCTGCC	80176
rs562963704	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9348514	CCAAACAGTGCACTT[G/T]GGGGATGCTTTTGAC	80176
rs562975820	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9348929	CATCCCCTTTCACTC[A/G]TGCAAGAATGTGTGT	80176
rs562978219	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9340374	ACCAGCCCAGCTGCC[A/G]ATACAATTAAACCTC	80176
rs563028214	snp	A/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9326055	AGTGACCTGTCCCAC[A/T]CCACCCCTGCATGTC	80176
rs563097679	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9295995	AGTGAAATCCAGACT[A/C]TAAGGGACTTCGATT	80176
rs563105247	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9353875	GTGAGACGAGATAGC[A/G]CCATTGCACTCCAGC	80176
rs563130106	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9358674	GCAGACAGACAGATG[A/C]GGGGACTGCCAGACC	80176
rs563154960	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9364349	CAGACCACAGGCTGC[A/G]ATAAGCACTTCTGGC	80176
rs563164229	snp	A/C	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9319135	GCAGTGAGCCAAGAT[A/C]ACACCACTGCACTCT	80176
rs563191414	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9353217	CTCGAGAGCCGCCTC[A/G]GCCCTCCCAGCCTTC	80176
rs563203544	snp	C/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9306636	AGCTGGGAGCTGAGC[C/T]CCAGCAGCCAGGCTC	80176
rs563229040	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9359125	GCGCTATTAGTCAGT[A/G]ACGAGGATGCTTTTT	80176
rs563229311	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9338271	CCCTGGCCGTGGGCT[C/T]CCCAGGACCCCTTTG	80176
rs563242667	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9326365	TGGGCCCCGTGGAAG[C/T]TCTTGGAGTCTCTGA	80176
rs563314563	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9304532	TATCCCTGACCTGCC[A/G]GTTGGGATGGAAGCT	80176
rs563372621	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9351875	GATGGCAGAAGTGGC[C/T]GGGTGTGTGGGCCAC	80176
rs563398158	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9305566	GGTCTGGGAGAGCTC[A/G]ATGTGGGCCCAGGGT	80176
rs563418867	snp	C/G	0	0	intron-variant	SPSB1	GRCh38.p7	1:9345337	CTGCTTTTGGGCCTG[C/G]CTTTCTGCTTCCACT	80176
rs563454436	snp	G/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9361776	TGGAGGGCAGGAGTG[G/T]AGATGGCCATTGCTG	80176
rs563480436	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9329024	ACTAGGGGCGGGCCC[C/T]GCATTTGCTGGAATT	80176
rs563514699	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9336505	TGCTGGGATTACAGG[C/T]GTGAGCCACCACGTC	80176
rs563571586	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9292255	TGTTCGGGGAAGGGG[G/T]AGGAAAATTCCTTGA	80176
rs563588548	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9362583	GCATTCTCTGATGCG[G/T]AACATTTTTCCTTGA	80176
rs563626496	in-del	-/GGGGC			upstream-variant-2KB	SPSB1	GRCh38.p7	1:9292797	GTGCGCCCGAGGTCG[-/GGGGC]GGGGCGGGGCGGGGC	80176
rs563633870	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9320134	CTTCTCACCGGCCCC[A/G]CCCCCCACTATAGTT	80176
rs563650328	snp	A/G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9335763	CAGTGAGCCATGATC[A/G/T]TGCCACTGCACTCCA	80176
rs563676201	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9315256	CCAGCTCAGCAGATT[C/G]CACTGCGACAAAAGA	80176
rs563679863	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9324960	GCGGGCTGGTGGATC[A/G]GAGGCGCCTGTGAGC	80176
rs563694972	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9320585	ACACAGAGGAAGCAC[A/G]CAGCCCTCTCTTCCA	80176
rs563713939	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9309613	TTTGGGAGGCCGAGA[C/T]GGGTGGATCACCCGA	80176
rs563773990	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9367646	CCTGCCGCTGGGGCC[A/G]CCGCACCCTGCACCT	80176
rs563787790	snp	G/T	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9324554	AACCAGCTTGGGTGG[G/T]GAGGGGGAGTCAAGA	80176
rs563799202	snp	A/C	0.0614824	0.164198	intron-variant	SPSB1	GRCh38.p7	1:9309230	GTGCAGATAAGCTAG[A/C]TCCCCCCTCAATTCC	80176
rs563824448	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9342517	GAGCTGCCTCAGGGT[A/G]TTGACCTGCTCAGTG	80176
rs563864060	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9299956	GCAACAGAGTAAGAC[C/T]CTGTCTCAAAAAAAA	80176
rs563876610	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9315081	CACTGGTTTAAAATA[C/T]AACATCTTGTGGGAT	80176
rs563880013	snp	A/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9329906	CTATGAGGCCTTTGG[A/T]ATCTTTTCTGGGACT	80176
rs563895392	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9341771	ACAATAGCGCGATCT[C/T]GTCTCACCGCAATCT	80176
rs563900957	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9300275	GACTTTGGAGGCAAC[A/G]CATTCCTCATTTGGG	80176
rs563926036	snp	C/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9314032	AATACAAAAATTAGC[C/G]AGGTGTGGCGGCGGG	80176
rs563940002	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9305406	GGGCAGCCCAGTGAC[C/T]TGTGGGCTCCAGGAG	80176
rs563965386	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9314447	GAGCATCTAGACCCC[A/G]ACTGCCAACCCACCT	80176
rs564008356	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9294229	GTGTGTCTTTGCGTG[C/T]GTGTGTCTTTGTGTC	80176
rs564077712	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9335793	AGCCTGGACGACAGG[A/G]CAGGACCCTGTCTGT	80176
rs564101206	in-del	-/CGCGCCC	0.029116	0.117091	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9292724	CCAGCGCCGGGCTGA[-/CGCGCCC]CGCGCCCCGCGCCCC	80176
rs564107455	snp	A/G	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9305027	CCCTGGGCTTCACCT[A/G]CCTCCTGCGCCCAGA	80176
rs564142652	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9300016	TTACATTGATGTCAT[C/T]ATGCTTCATTGGACC	80176
rs564148547	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9335915	TGTGCACAGTAGTAA[C/T]GATAGCTACCACCTA	80176
rs564156046	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9352219	GAGAGGTTGTGGAGC[C/T]GACCTGGACAGACAG	80176
rs564158396	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9346192	ACTGATGTGTGAGAC[A/G]GGGCGGCAGAGGGAG	80176
rs564209354	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9341104	TTTCCACTTCCCCTT[C/T]CTTCCCCTTGTGTTC	80176
rs564238836	snp	C/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9356785	GATTACCTAACGGTG[C/G]CTCATGAATGAATGG	80176
rs564249340	snp	G/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9324381	CGATCCTGTGGCTCA[G/T]CACGTGGTAGGTCCT	80176
rs564254171	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9352481	CGCGTTTATTTATGT[C/G]CCGTCTGTGGCTGCT	80176
rs564291033	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9330894	ATACCCAAGGGTTCC[A/G]GTTTCTCCACATCCT	80176
rs564354662	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9325328	GTCTGGGCTGTGTGG[C/G]ATTGAGCTCTTGCCA	80176
rs564375116	snp	C/G	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9358021	CAGGCAAGAGGCAGA[C/G]GGGGGTGAGGCCCCC	80176
rs564439979	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9299640	ATGCGCCACCACACC[C/T]AGCTAATTTTTTGTA	80176
rs564479251	snp	A/G	0.00398564	0.0444627	intron-variant	SPSB1	GRCh38.p7	1:9330572	TGGACCTTGTGATCT[A/G]GACACACGTATCCCT	80176
rs564494121	snp	A/G	0.0289422	0.116762	intron-variant	SPSB1	GRCh38.p7	1:9320888	GTGAGCTCTGGCCAC[A/G]AAAGGCTGGCCTGAT	80176
rs564528412	snp	A/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9316417	GTGCATATGTGCTTG[A/T]GTGTGTGTCCCCACA	80176
rs564531910	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9353058	AGCTGACCTCTGTGC[C/T]CACAGGACCCTGCAA	80176
rs564567814	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9355535	CACAGTCGGCCGCGT[A/G]GACAGACAGACCCTT	80176
rs564567824	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9349473	AGAGAGGCCAAGGGA[C/T]GTGGAGCGTGAGAGG	80176
rs564577098	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9300326	GCTGAGTCACCCTAA[C/T]GCTTCTAGTTTTGAG	80176
rs564585632	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9366491	GGCTAAGGGCATGGA[C/T]GCTGGGCCCAGGCTG	80176
rs564624600	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9327721	CAGCAAACTTTAAGA[A/G]CCTGATGGTAATGAT	80176
rs564660593	snp	A/T	0.00557542	0.0525036	intron-variant	SPSB1	GRCh38.p7	1:9295207	GTGTGTGTGTGTGTG[A/T]GAGAGTGTGAGTGTG	80176
rs564690110	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9362713	ACAGTTGTGGGTTGG[A/G]GCTCTGGGGCTGTGC	80176
rs564692192	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9300950	TCTGCACTATATGAA[A/G]GCACAACCCGAAAGT	80176
rs564699234	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9295689	CCTCCCACCCCCATG[A/G]TGTGTGCCGTGCTCC	80176
rs564711051	snp	A/G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9333627	TGAGCCACCATGCCC[A/G/T]CCCTCCTTGTCAGCT	80176
rs564733509	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9347860	CTAGAAGGCTGCCCC[A/T]GTTCAGGGTCTGTCC	80176
rs564838675	snp	A/G	0.00478085	0.0486577	intron-variant	SPSB1	GRCh38.p7	1:9336940	TTCTGGTGCCTGCTG[A/G]TCCCCACTGAGGGGC	80176
rs564860384	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9317963	TGCCAGGCTCGGCCC[A/G]AGCATCTGTGGAACC	80176
rs564875015	snp	C/T	0.00279162	0.0372561	intron-variant	SPSB1	GRCh38.p7	1:9312629	AACACAGTCAGGTGC[C/T]AGCACGGAGTTTTGT	80176
rs564876303	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9333118	CTCCATGGGAAAATG[A/G]CCAGAAACATGGAAC	80176
rs564922065	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9366492	GCTAAGGGCATGGAC[A/G]CTGGGCCCAGGCTGC	80176
rs564953412	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9360676	GTGCTCCACCTGTGT[A/G]TGTGTCTCTCCGTGG	80176
rs564968688	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9293211	GGGCCGGGCGCGGGG[A/G]AGCGGGTGGAGTACG	80176
rs565124835	snp	A/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9299549	CAATGGTGCAATCTC[A/G]GCTCACTGCAACCTC	80176
rs565137781	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9302429	TTGGAGGACACTGGC[A/G]ATTGAGTCACTCAAC	80176
rs565166273	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9338818	CTTCCTGGGGGCGCT[C/T]CCGCCTTGCTCTGCT	80176
rs565214785	snp	C/T	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9340280	TCAGCAGAGGAGGGG[C/T]CTGGGGGGGAAGGCA	80176
rs565223531	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9346119	TGCAGAGATTGATTC[C/T]GATAAAATAGCAGAT	80176
rs565229711	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9349751	TGAGGAAGGTCCTTT[C/T]GGGAGTTCCCAACCC	80176
rs565239012	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9313194	CCAAGGTTTGGAGTT[C/T]GAGACCAGCCTGACC	80176
rs565269650	snp	C/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9305861	CTGCTGATGATAGCG[C/G]TCAGGGTATCAGAGG	80176
rs565272950	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9339497	CGTGGAGGAGGGGCC[C/T]CTGGAAGATCCCACA	80176
rs565327975	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9361851	ACCCTCCCTGGAGAT[G/T]TGGAAAGGCCTGTTT	80176
rs565332093	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9299293	TATCAGCTCTCCAGC[C/G]CTATGTCACAGTTTA	80176
rs565348129	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9314468	CAACCCACCTTCTGC[A/G]GACCCAGAGGGCTGA	80176
rs565350619	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9326817	CTGTGTTGGTTTAAT[C/T]GGAAAGGCTTATTGC	80176
rs565418375	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9335038	CAAGGCCCTGCTTTG[C/T]ATTTATTTGAGTGAA	80176
rs565445731	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9339930	GGAGAGGGATGGGAG[C/T]CCCTCCACCTTTTCC	80176
rs565453792	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9308029	CTGTTTCCAGGATTG[A/G]TTGCTGACAGTATTG	80176
rs565490455	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9303878	AGATGGTAAAGCATT[C/G]ATGATTCTCAATGCT	80176
rs565586440	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9349078	TCATCTGGTGTCCCC[A/G]CAGGTAGCCCCTCCC	80176
rs565601278	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9349490	TGGAGCGTGAGAGGC[C/T]GAGGCCTTGGCGCCA	80176
rs565616195	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9307702	TCCCTCATCACCAGA[C/G]ACTCAGCCACCATCC	80176
rs565650747	in-del	-/AAAAC			intron-variant	SPSB1	GRCh38.p7	1:9319185	GACTCCATCTCAAAA[-/AAAAC]AAAACAACAGTAACA	80176
rs565658026	in-del	-/ATAC	0.00993419	0.0697739	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9369042	AAATGTTTAATATAT[-/ATAC]ATACATATATATATA	80176
rs565680726	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9322313	GGGGAAACTGAGGTT[C/T]GGAAAGTCTCTCAGG	80176
rs565683986	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9312710	TGGACTCATCTCATC[A/G]AATTGGCGTGGTTTT	80176
rs565705466	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9339489	GAAGGCTCCGTGGAG[G/T]AGGGGCCCCTGGAAG	80176
rs565754916	snp	C/G	0.00279162	0.0372561	intron-variant	SPSB1	GRCh38.p7	1:9318021	TTTGGTGACGTGCCA[C/G]GTGGGGAGAGGAAGC	80176
rs565783453	in-del	-/GGATAGACCTGAGTGCGCACAGGACAC			intron-variant	SPSB1	GRCh38.p7	1:9301535	GGGGAAGATGTATGT[-/GGATAGACCTGAGTGCGCACAGGACAC]GGATAGACCTCCCGA	80176
rs565783874	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9355121	TTGAGAAGAATGTAG[C/T]TGGCGGAGGAGGCTC	80176
rs565802999	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9361999	GCATTTTCGAATTTT[C/T]TTTAACGGCTCCCAG	80176
rs565823155	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9317353	TTGATGATACCCGGT[A/G]TATAGTAAGTGCTTG	80176
rs565875554	snp	C/T	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9312134	AGACACATGCCACCA[C/T]GCTTGGCTAATTTTT	80176
rs565950020	snp	C/T	0.00199481	0.0315187	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291221	GACGGAGTCTCGCTC[C/T]GTCACCTGGGCTGGA	80176
rs565988952	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9350715	CCCTTTGCGTCTGCT[C/T]CTCCTGGGTGGGGAT	80176
rs566035954	snp	A/G	0.00438332	0.0466095	intron-variant	SPSB1	GRCh38.p7	1:9319330	TGCGCTGCCCTGGCC[A/G]TGGCATGTTGCTCAC	80176
rs566061528	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9365887	AGAACAGCGTGGGCG[A/G]CCCCACGAAGGTCCA	80176
rs566112242	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9328629	GGTGAGCACCAACGC[C/G]CCACCCACTGCCTCC	80176
rs566124732	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9307287	CATTTTAAAGTGAAC[A/G]GATCAGTGGCATTTG	80176
rs566137683	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime	SPSB1	GRCh38.p7	1:9355830	CAGAATACTGGAGAC[A/G]AGACCACGAGATTGA	80176
rs566160943	snp	C/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9323411	GTGGAGCCTCCCTCG[C/T]GGCCCGTTGGCAGAG	80176
rs566192084	snp	C/T			upstream-variant-2KB	SPSB1	GRCh38.p7	1:9292028	TCCTCGCCTTTACAG[C/T]GAGTGTGTCATTAGT	80176
rs566209369	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9318733	GCAATTCGGGCAGCT[C/T]ACTCAGATCAGGGCC	80176
rs566247143	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9327641	TAGGACAGAGTCTTG[A/G]GGGAGTGTGGGGGAG	80176
rs566252805	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9334625	GAACTTTCTTATCTT[C/T]CCCAACGGAAACTCT	80176
rs566310140	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9338731	GAGGTCTGAGGGGGC[A/G]TCACCTCCCCCATAT	80176
rs566314823	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9316276	CCCTCCCTGTGGGTG[A/C]GTCACCTGCTTTGGG	80176
rs566320361	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9298925	GTTGCCTCTGCCTGG[G/T]AAAATAGTACATCAA	80176
rs566331127	snp	C/G	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9352748	CCTCGCCTCTTCCCC[C/G]CTCAACCTCCCTGTT	80176
rs566331461	snp	G/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9363550	ACCTCCCCAAGCCCA[G/T]TTCCCTATCTGTAGG	80176
rs566348579	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9355694	CGGGTTAACTTTCCC[C/T]TTCATCCCACAGTCC	80176
rs566359121	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9333979	AGCATCAGGACAGAC[A/G]GACTCCATTCATCAC	80176
rs566457609	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9367964	TGGTGGGGGTGGCAG[A/G]TGGTACCACAGCTCT	80176
rs566471113	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9316560	GGATGGCGAGGAGGG[A/G]GGGGCTGATCGAAGC	80176
rs566495692	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9326762	CAGAAATGGTAAGCC[C/T]GCTGCTTCTGAGGGG	80176
rs566503235	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9293423	GAGGAGGGGCTGGGG[C/G]GCTCCGGGGCCGCCG	80176
rs566550864	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9325629	CTGTGCCAGCCCCTG[A/C]GGCACAGTGTGAACA	80176
rs566610687	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9300486	AGGCCCCTGTAGATG[A/G]ATCGCAGTACAGGCC	80176
rs566612847	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9363257	TTATGTACTTGAGGA[C/T]CCAGAGAAGAGACCC	80176
rs566640547	snp	C/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9325189	CAAGAAGACCTGTAC[C/T]CCGCCCTCCGGCCTG	80176
rs566645414	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9336693	GACGCAACTCCTGGC[C/T]GGCTCGGGCAGGTCC	80176
rs566658171	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9301198	AAGATTGGTGACAAA[G/T]AAAGCTGGGGGCCTG	80176
rs566706388	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9306557	ACCTATAGGGTAGGT[A/G]CTACCCATTTTACAG	80176
rs566718503	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9333195	TCCCAGAGGGACCAG[C/T]ACAGCCATCTGTCAC	80176
rs566734454	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9306135	GGGGTTGCTAGAGGG[C/T]GAGCCTCACCCTTGA	80176
rs566743462	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9307011	CAGCTCACTGCAGCC[C/T]CCGCCTCCCAGGTTC	80176
rs566755131	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9359437	GGCTGGGCGCGGTGG[C/T]TCATGCCTGTAATCC	80176
rs566763773	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9337297	GGAGGACAAGAGTTG[A/G]CCCTGAAGTCCCTCT	80176
rs566776892	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9330770	CTTAACCATTTAAGA[C/T]GTGCAGTTCAGTAGC	80176
rs566779186	snp	A/G			utr-variant-3-prime	SPSB1	GRCh38.p7	1:9367689	CGTAGCCATGGACAG[A/G]GGTCCCTGGTCTTCC	80176
rs566814834	snp	C/T	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9296736	CTCAAAGAGGTTGAC[C/T]GTTACTCTATGCGGG	80176
rs566827790	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9295408	GGCGGGTGCCATGCC[A/G]GCTTAAGAGAGACCT	80176
rs566861148	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9364751	GCTGTGGCTGTGACC[A/G]TCCATGGGGGATGAA	80176
rs566873374	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9365058	GATGAGGGTTCACCA[C/T]GTTGGCCAGGCTGGT	80176
rs566902991	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9352907	GTGAATCTTCCATGA[C/T]AGACGAGATCCCGGG	80176
rs566951784	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9318096	GATTGTTCTGGGAAG[C/G]TGCAGCTTAGGGAGA	80176
rs566986207	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9341860	GGCATGCACCACCAC[A/G]CCCAGCTAATTTTGT	80176
rs566990320	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9359340	GGCGCGGGTGTTAGC[A/G]CTGCCAGCCTCAACC	80176
rs566997419	snp	C/G	0.00119737	0.0244387	downstream-variant-500B	SPSB1	GRCh38.p7	1:9369871	GAACTTGAGTTGACC[C/G]TGGGCTTTTTAGGAG	80176
rs567087057	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9369201	CCCCCTTATTATTTT[A/G]ACGGTTTTTTTTTTC	80176
rs567118086	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9311081	TTCTTCTCCCGCCTC[C/T]AGCCTCCCAGGCTCC	80176
rs567129842	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9348063	GATTCTCCTGCCTCA[G/T]CCTCCCGAGTAGCTG	80176
rs567130550	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9358879	GGAGCCTATTTGAAC[A/G]GAGGGTTCCGCCCAC	80176
rs567172344	in-del	-/T	0.00953873	0.0683987	intron-variant	SPSB1	GRCh38.p7	1:9327262	CCAGTTTCATTTCTA[-/T]TTTTTGGGATGTGTG	80176
rs567193374	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9363633	TGGGGCTGGGGCTGC[A/G]GTGTCAGCCACTCAA	80176
rs567205096	in-del	-/AG	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9336610	GCGTGCGTTCAAGGA[-/AG]AGTCTGGGGCAGAGG	80176
rs567219537	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9353441	AGATGGAACTAAAAG[C/T]TTGAAAATGGGATTT	80176
rs567235712	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9354045	TTCTGCCAGGACCAA[A/G]CTTCCTGGAGACCTG	80176
rs567237241	snp	C/T	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9316868	CGGACCTTGTGACCT[C/T]TCTGAGCCTCAGTTT	80176
rs567298722	in-del	-/GAAT			intron-variant	SPSB1	GRCh38.p7	1:9341137	AAAATGTGATAAATG[-/GAAT]AGGCACACCCCAGAT	80176
rs567298729	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9348723	CCCAGACAACCTTAA[A/G]TGGCTGTTCGAAGCT	80176
rs567374101	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9298102	AGAGGCAAAGCTGCC[A/G]TCAGAATAGTCTGAC	80176
rs567397979	snp	G/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9316576	GGGGCTGATCGAAGC[G/T]GGTTCAGGGGCTGCC	80176
rs567401224	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9295900	AAAATTTTATCAGAC[A/G]ACAGCACAAGGTCAG	80176
rs567425934	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9326137	GGTCGGGTGGAATGT[C/T]CTTGGTGGGGCTGAA	80176
rs567447857	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9331295	TAAATACCCGTTATG[A/G]ATCTCCTTCTGCTAC	80176
rs567452439	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9296486	ACACCAAAGTTAGAG[A/G]CAGAGTATAATGAGC	80176
rs567460099	snp	A/G	0.0119091	0.0762411	intron-variant	SPSB1	GRCh38.p7	1:9325674	CCCCTGTGTTCTCAC[A/G]GGGGACGGGTCTTAA	80176
rs567500328	snp	A/C	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9302101	GCCGGTGAGCACGAG[A/C]CCACTGGTTTCGCCT	80176
rs567525419	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9301648	CTCTTTCCCTGGCCA[C/T]CCCTGTCATCGCCTG	80176
rs567533106	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9297444	AGTGTGGCCAATCTG[A/G]TCACACCCTTTCCAA	80176
rs567536881	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9302534	CTGGCTCTCTGTCCC[A/G]GAGCTGGGATGCTCT	80176
rs567560999	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9303926	CATCCCTTTTCTGCT[A/G]ACAGGGAAGCCCAGT	80176
rs567580887	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9368903	ATCCCTGGCAACCCC[G/T]CCACGTAGCGTACCC	80176
rs567581813	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291759	AGCACCCCTAAGCTG[C/T]TGGCCATGGCTGCCC	80176
rs567640885	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291309	TCCTGCCTCAGCCTC[C/T]CAAGTAGCTGGGACT	80176
rs567647679	snp	A/G	0.00279162	0.0372561	intron-variant	SPSB1	GRCh38.p7	1:9360215	GGCCAGGAGGGTGGG[A/G]GCTGAAGGGACCCAG	80176
rs567688971	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9324695	CCTGGCAGGAGGCAG[C/T]GGCCAGCCAGCATCT	80176
rs567708131	snp	C/T	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9360851	GGACACTGGTCAACC[C/T]GCTTCAGATGTGGAG	80176
rs567717911	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9365120	CCTCGGCCTCCCGAA[A/G]TGCTGGGATTACAGG	80176
rs567740691	snp	A/G	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9307285	GCCATTTTAAAGTGA[A/G]CAGATCAGTGGCATT	80176
rs567753071	snp	C/T	0.00119737	0.0244387	downstream-variant-500B	SPSB1	GRCh38.p7	1:9369953	AGCAGGTCCTTCATT[C/T]GTCTTTGTGTCCCCT	80176
rs567774627	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9300117	AATTCTACTGAAATT[C/T]GGGGACCTTCTCCCT	80176
rs567845019	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9342748	CCGGAGAAACTCCAT[C/T]TACAGGTGCTGTCTC	80176
rs567904208	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9307674	AATAGGAACACCTGT[C/T]TTTCTGTCCATATCC	80176
rs567912325	snp	A/G	0.00279162	0.0372561	intron-variant	SPSB1	GRCh38.p7	1:9307054	CTCCTTAGCCTCCTG[A/G]GTAGCTGGGATTACA	80176
rs567935594	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9305065	GGCATTGCCTTCCCT[A/C]CAGGGGCCTCTCCCA	80176
rs567961710	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9294709	ACTAAGGTTTGATGT[C/G]CTTGGAAGAATTTTC	80176
rs567993115	snp	A/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9307021	CAGCCTCCGCCTCCC[A/G]GGTTCCAGTGATTCT	80176
rs568039685	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9367749	AAGGACCGATTCCAA[C/T]ACAGGCTCCTCTTTC	80176
rs568058473	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9335990	TGCAGAGCTGTGTAA[A/G]CATCCAGCACTGTTT	80176
rs568066515	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9362826	TGCTCCCAGAAATAG[C/T]GCCTGATTGACTTCC	80176
rs568070382	snp	A/G	0.00517822	0.0506191	intron-variant	SPSB1	GRCh38.p7	1:9357185	TGGGTGGATGGATGA[A/G]TGGATGGATGGATGG	80176
rs568093440	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9367230	GTGAGGATTAAATGA[A/G]TGTTAGCAGAGGGCT	80176
rs568173405	snp	A/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9342153	CAGAGCACAGGCCTC[A/T]GATGGTGGAGTTCTC	80176
rs568188771	snp	A/G	0.00874735	0.0655527	intron-variant	SPSB1	GRCh38.p7	1:9364876	GTTTTTCTGAGACAG[A/G]GTCTTGCTCCGTCAC	80176
rs568197222	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9318849	GTGATTGTAACACAG[G/T]GTGACAAAAGAGGAG	80176
rs568259382	snp	A/G	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9339659	CCTGTCAGGGGCTTG[A/G]AAGGTGGAGAGCAGG	80176
rs568268498	snp	A/G	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9299726	CCAAGTGATTCACCC[A/G]CCTTGGCCTCCCAAA	80176
rs568278721	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9335359	ATACAAAAATTAACC[A/G]GGTGTGGTGGTGAGC	80176
rs568322879	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9345743	TTGGGTCTTTTGAGG[C/T]CAGGGACTAGAGCTC	80176
rs568325230	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9350274	GCAGCCTGAGGGCTG[C/T]GGACAGGAGAACTGT	80176
rs568345873	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9331745	TTGGTACTTGCTCTC[C/T]GCTTCCTGTGTGTAG	80176
rs568370340	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9368493	GGCTGCAGCAATTCC[C/T]CTGTGTCTCCAGGTA	80176
rs568383816	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9330351	TGGTGGTGCATCTCT[A/G]CTACTCAGGAGGCTG	80176
rs568388756	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9340621	GCAGCCTGTGGGGCT[A/G]GGGAGGGTCCCCGCA	80176
rs568388805	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9346288	ATTTCATTCTTTCCC[C/T]ATCTTGGGGCAAAAC	80176
rs568408788	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9302012	CACTGTCACGCTGTC[C/T]GTGTAGCACTGCTTC	80176
rs568443919	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9306227	TCCTTTCGGGTGTGC[C/T]GAGGGATGGCCGAGC	80176
rs568458959	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9320306	TATTGCCTCTTGGGC[C/T]GGGACTGTCCTCTGT	80176
rs568498752	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9347576	TGTTCTTTCAGAAAC[A/G]GCATCATGATCTGCA	80176
rs568528366	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9315423	CGTTGTCTCACGCAA[A/G]TCTTTACAATACAAC	80176
rs568544749	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9352132	TGGTTCAGGTTAGGT[G/T]TAGGGAGCTCAGCCC	80176
rs568567938	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9295248	TGTGTGTGTGCGCGC[A/G]TGCGGTTGGGGAGGT	80176
rs568589830	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9344726	TGGGCCTCAGGGGGC[A/G]GATGAGTGGATGCCC	80176
rs568595796	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9326003	GACAGAGTGTCCTGG[A/G]TCCTGGCCAGGAGGA	80176
rs568706050	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9349098	TAGCCCCTCCCCCTC[A/C]TCCAGAGCTTTTAAT	80176
rs568711081	snp	A/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9320416	GCCCTGCCCCACGTG[A/T]GTGCAGATATGGGGT	80176
rs568724947	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9300387	CCAGGTTGCTGTGCA[A/G]CCTGCTTTGCCACTT	80176
rs568740139	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9357542	GTGACCTCTCTCACT[C/T]ATTAGACAGGCTTAG	80176
rs568808088	snp	G/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9325549	ATGGTGGTGTGAGCA[G/T]GTGGCACCGTGGAAC	80176
rs568819916	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9363517	CCATGGCTCTCAGAC[C/T]TTGGACCTGTAACTC	80176
rs568832687	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9362876	TCAGCATTGCACTCT[C/T]ATTCACAGAAATTAT	80176
rs568847950	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9357748	CATGTGTAGGGGCAC[C/T]GTGCTGGTGTGGGAG	80176
rs568883329	snp	A/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9309998	GCTGTGGGTCTGCCC[A/G]AGGTCCTGGGCTTCT	80176
rs568890028	snp	C/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9311075	GATCCTTTCTTCTCC[C/T]GCCTCTAGCCTCCCA	80176
rs568901444	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9336699	ACTCCTGGCCGGCTC[A/G]GGCAGGTCCCTCACT	80176
rs568911885	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9352247	CAGACAGTGGATGTC[C/T]CACGTCAAGGTGAAG	80176
rs568968666	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9367806	GCATCCCTGCATGCC[A/G]TCCGTATACAACCCC	80176
rs569010880	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9337887	CAGACCCAAGAGCAC[A/C]TTTAGGGGCGGGAGG	80176
rs569031497	snp	A/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9367319	AAAATGAAAAAGCAT[A/T]GCATTTTTCATTGTT	80176
rs569038788	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9330168	TGACACCTGATATGT[A/G]CACATAAAGATGTAC	80176
rs569095339	snp	A/G	0.00676609	0.0577691	intron-variant	SPSB1	GRCh38.p7	1:9305164	GCCACTGTCACCTAT[A/G]TTCTGCTGACCCCGT	80176
rs569099221	snp	A/G			downstream-variant-500B	SPSB1	GRCh38.p7	1:9369989	TGAGTGCACGGTGAT[A/G]TTTGCTGAACTGTTG	80176
rs569169364	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9364176	CCTCCACTTTCCGGC[A/G]GGGGCTGAGCCACAT	80176
rs569174933	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9336257	TTTGAGATGGAGTTT[C/T]ACTCTTGTTGCCCAG	80176
rs569255156	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9330867	CTGTGCCATTTTGCG[C/T]TTCCATCAGTGATAC	80176
rs569272649	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9369179	ACTGGGTGAGAAATG[G/T]ACATTACCCCCTTAT	80176
rs569286536	snp	C/G	0.000798403	0.0199641	downstream-variant-500B	SPSB1	GRCh38.p7	1:9369792	AGCTGCAGAAACTTG[C/G]CAAGTCTAACAGACA	80176
rs569290878	snp	A/G	0.357238	0.225832	intron-variant	SPSB1	GRCh38.p7	1:9296606	TACACACACATACAT[A/G]TGCACACACATATAT	80176
rs569293599	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9301435	AGCCTAGGAGGTTGA[C/G]GCTGCAGTGAGCTGT	80176
rs569345595	snp	C/G	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9334736	CTGGCAACCACCATT[C/G]AACTTTCTGTCTCTA	80176
rs569468522	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9347681	GCTGCATGGAGCTCC[A/G]TGGTGTAGATGAGGT	80176
rs569515848	in-del	-/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9311827	GTTTGGTGCATCCCT[-/G]GGGGGGTATGAATTT	80176
rs569521200	snp	C/G	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9320761	TTCCTTTTGAAGGTG[C/G]CTGGAGGGTGACTCC	80176
rs569526339	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9352640	AGCCTGAGAGCTCCC[C/T]CCTCCTCCCTCCTCT	80176
rs569609489	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9344771	CACGTAGGCTGGGTG[A/G]TGGCCCCTGAAATCT	80176
rs569641443	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9366309	TTCCTGGGGCCTGAG[A/C]TTGGCCTGGGCCCTC	80176
rs569686874	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9299367	ACTGGGGCTGGGCAC[A/G]GTGGCTCACTCCTGT	80176
rs569706834	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9358319	TACAGGCTCCCAGGG[A/C]TGCTTGGTCCTCGTC	80176
rs569768755	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9356937	GGATGAATGTTTGGA[C/T]TGATAGATAAGTGGT	80176
rs569795287	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9349943	ACATATGCATACACA[C/G]ACACAGACACACGCC	80176
rs569798017	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9312776	TTTTTTCAACCTGGT[A/C]AGTCTTATTGCAAGT	80176
rs569805007	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9303329	CTTAAAGAACCACAG[C/G]CAGCTGAGGTGCTTG	80176
rs569849756	in-del	-/TTT			intron-variant	SPSB1	GRCh38.p7	1:9347945	GTTTCCCTGCAACTT[-/TTT]TTTTTTTTTTTTTTT	80176
rs569861512	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9344284	CAGAAAGTCTAACGG[C/G]ATCAGGAATTTGCAT	80176
rs569903640	in-del	-/C	0.00119737	0.0244387	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9369306	AATGTTTCCCTTGTA[-/C]AGATCCCAGCTTATG	80176
rs569921510	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9355157	GCCTTTCGTGCCAAG[C/T]GCACACAGACCCCTG	80176
rs569944424	in-del	-/TTC	0.00318978	0.0398085	intron-variant	SPSB1	GRCh38.p7	1:9318702	CCATTCAGAGGGTTG[-/TTC]TTCTGTCCATTCAGC	80176
rs569950462	snp	A/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9349547	CAGCTGATCTCTGAC[A/T]CAAGGCGTGCAGGAG	80176
rs569986614	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9361594	GGCCGTGGCCGGGCG[C/G]AAGTAGGGGTACTGA	80176
rs570030273	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9314754	CTGTGGCCATTTCTA[C/G]TGGCAAGTGGCTGAG	80176
rs570062937	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9322545	AGGAGGGATGGCAAT[C/T]ATGATGAGGGCTCAG	80176
rs570144060	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9306137	GGTTGCTAGAGGGCG[A/G]GCCTCACCCTTGACC	80176
rs570151174	snp	A/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9319424	CTCCTTCCTCCCTCC[A/T]CTTCCTCCTTCTCCT	80176
rs570151934	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9345820	CAGAAGGATCCTGTT[C/G]TTTTTTGTTGATTCT	80176
rs570188746	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9314137	GCTGAGATCGCACTA[C/T]TGCACTCCAGCCTGG	80176
rs570204642	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9334838	TTTACTTCATATAAC[A/G]TGTTCAAGATTCACT	80176
rs570251998	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9293756	ACCGTCCCCGGGCGT[A/G]TACTGGGCTCGGTGG	80176
rs570278797	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9321218	CGTCTCAGGCGGTGG[A/G]CCTTAAACATTTACA	80176
rs570280970	snp	G/T	0.00398564	0.0444627	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9292723	AACCAGCGCCGGGCT[G/T]ACGCGCCCCGCGCCC	80176
rs570339427	snp	A/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9323604	AGATGTAAACAAAGC[A/G]GAGAAGGGAGAATGG	80176
rs570412708	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9304601	CTAGTTGAATGTGGG[C/G]TGTAGAGAAGGGTGA	80176
rs570450599	snp	C/T	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9366762	TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT	80176
rs570459274	snp	A/G	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9335323	CCTGGCCAACATGGC[A/G]AAACCCCGTCTCTAC	80176
rs570461771	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9313417	CATTTTCTATAAAAT[C/G]AAATAAAATAAAATA	80176
rs570541447	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9331492	TGCGCCACCATGCCC[A/G]ACTAATTTTTTGTAT	80176
rs570563630	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9346511	TCTTCCTAAAACACC[A/G]CCACAAACAGGTAAT	80176
rs570627303	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9346883	TAGAGAGAGACAGCC[G/T]CCCCATTTTTACGGG	80176
rs570648780	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9304162	TCCTGCACTCGGATG[C/T]CACAACTCCAGGTTC	80176
rs570710113	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9350018	CACACACAGCACATA[C/T]ATACACACATGAAGA	80176
rs570718249	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9366426	AGCCAGGCCTGTCAC[A/G]TATGATTCAGGACAG	80176
rs570750428	snp	A/G	0.00279162	0.0372561	intron-variant	SPSB1	GRCh38.p7	1:9351426	TGGAAATGCAATAAC[A/G]CCAGCCCTCTCTGGA	80176
rs570775498	snp	A/C	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9344962	CACTGGCTCCCATTC[A/C]GGCCTTGGCACCCTG	80176
rs570790808	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9329968	GGATGACAGGACAGC[A/G]GGTTCAGAGTGGCCC	80176
rs570845226	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9309786	GGCAGAGTTTGCAGT[C/G]AGCCAAGACTGCACC	80176
rs570943919	snp	A/C	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9357073	TGGATGGATAAATGA[A/C]CGGATGGATGGGTGG	80176
rs570963536	snp	A/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9354603	GGATCACCTGAGGTC[A/T]GGAGTTCAAGACCAG	80176
rs570966405	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9314871	AGGCAGCCAGTGGGA[G/T]GCTCCAGGGCAGGGA	80176
rs570972858	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9315289	CCGTACTGGCTCCAA[A/G]GGACACAGCCCCGTG	80176
rs570988513	in-del	-/G	0.00279329	0.0372672	intron-variant	SPSB1	GRCh38.p7	1:9338724	CCTTTTGAGGTCTGA[-/G]GGGGGCGTCACCTCC	80176
rs571096335	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9323818	AGGAATACATTTCTT[A/C]TGCTGTTGCCCACGG	80176
rs571103971	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9324120	TAGGTTTTTCAGTCC[A/C]TATCTTTTTTTGTGT	80176
rs571173395	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9322837	GTAGGGAAGCGCTGC[A/G]TTAGGTCACCAGGCA	80176
rs571246535	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9343854	GCAGTGGCGCGATCT[C/T]GGCTCACTGAAAGCT	80176
rs571249922	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9312025	GCCTGTCTCTGTCAC[A/C]CAGGCTGGAGTGCAG	80176
rs571330622	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9343075	CATTTATGTGTTTTG[C/T]TTTTATTGAGGTGAA	80176
rs571372479	snp	A/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9321661	TTCACCTTTAAATAA[A/T]AAAAAAAATGCTGCT	80176
rs571405398	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9359375	TAACCCGACACCTCT[C/G]GACGCTTATTGAGGC	80176
rs571423598	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9313368	TTGCACCACTGCACT[C/G]CAGCCTGGGCAACAA	80176
rs571479199	snp	A/C	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9316927	CCCCCGGGTAGAGGG[A/C]GCTGCCTGGTGCTCT	80176
rs571490769	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9364666	TCTTAATCATCCTAA[A/G]CTGGCCACGAAAGGC	80176
rs571503976	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9298136	TGTGGATCTATGGCA[C/T]TGGATAGTTAATCAT	80176
rs571522682	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9297286	TGATTTGAGCACAAG[A/G]TGAAGAAAATATCAG	80176
rs571537905	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9361489	GCGTGTGTGCCTTCC[C/T]GGGGGTCTCCCAGCC	80176
rs571555500	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9326697	GGTCAGCTGCTTCCA[A/G]AGAAAAACAGCAGCC	80176
rs571589937	snp	C/T	0.00199481	0.0315187	utr-variant-5-prime	SPSB1	GRCh38.p7	1:9355811	AATTCTGTCTGGCCC[C/T]GATCAGAATACTGGA	80176
rs571621187	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9334178	GCAACTTCCGCCTCC[C/T]GGGCTCAAGCAATTC	80176
rs571645319	snp	G/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9355215	GCCCTTTTCTGCAGT[G/T]AATTGGTGGTGCGTC	80176
rs571658328	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9305600	GGTGCTGGGGGTGGG[A/G]ACTCCCCGTCACGGA	80176
rs571689291	snp	C/G	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9360971	TCACGTCACCCCTAC[C/G]GATGCTGGGGTGCCC	80176
rs571727050	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9359911	GGCTCATCCATGGAC[C/T]GGATGTGACGAGAAA	80176
rs571727060	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9365341	AGGCTGGTCTCAAAC[C/T]CCTGGGCTCAAGCAG	80176
rs571752181	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9323065	ATGCTGGTGGTGGAC[A/G]GGCCAGGCGGCCGCC	80176
rs571771431	snp	A/G			upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291601	TTATTTAATTTTTGT[A/G]CAGAGTCTGTGTCTT	80176
rs571833144	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9327359	TCTTTGGCAGATACA[C/T]GCTTAAAAGTCGATC	80176
rs571852515	snp	C/T	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9339450	AGAGGTGCTCTGAGA[C/T]GGCTGCAGTGGAGGC	80176
rs571887949	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9349708	ATGCAGCTGTCTTCC[A/G]TGACTCACGGCCTCT	80176
rs571892190	snp	A/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9343154	TACATTCGCAATATA[A/G]TATACTACCACCTCT	80176
rs571896091	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9348853	ACCCCAACCCACCCC[A/G]TCCCATGGCTGCTCT	80176
rs571896902	snp	C/T	0.00318978	0.0398085	intron-variant	SPSB1	GRCh38.p7	1:9339086	CGGTGGAGCTTGCTC[C/T]GGCCAGGGCTGATCC	80176
rs571944512	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9351527	TGGATCTTGGTGGCC[A/G]GAGCTACTGTCTCGG	80176
rs571947089	snp	A/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9309551	CCTTGCATTTAAAAC[A/G]TGGTAATCAGGCCAG	80176
rs571957906	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9343551	ATGTTTTTGCAACAA[C/T]AACAAGACAACAGTA	80176
rs571966894	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9298256	GCAGAAACTTACAGG[C/T]CAAATGAAAAAAAGT	80176
rs571978993	snp	C/G	0.00953873	0.0683987	intron-variant	SPSB1	GRCh38.p7	1:9333533	ACGGGGTTTCGCCAT[C/G]TTGGGCAGGCTGGTC	80176
rs571980096	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9348293	GCTCCTGTCTCGGCG[G/T]TAGTGCTGTGTCTAG	80176
rs571983482	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9307970	ACCGACCCTGAGGCT[A/G]GGAGTCTGTAACTCA	80176
rs572029823	snp	C/G/T	0.000399281	0.0141238	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9290889	CTCCCAAGTAAACAA[C/G/T]AGTTCTCAAACTGCA	80176
rs572068625	snp	A/G	0.00119904	0.0244557	intron-variant	SPSB1	GRCh38.p7	1:9338724	GCCTTTTGAGGTCTG[A/G]GGGGGCGTCACCTCC	80176
rs572070957	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9339165	TCCTGCCCTCACCCC[C/T]CTTCTGTCATTCTCC	80176
rs572076370	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9307910	GTGCCACTCCCTCCT[C/T]GCCATGGTCCCCCTC	80176
rs572102970	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9327089	TTAGATGCATCTGCC[A/G]TCGTTTCGTGGGGAA	80176
rs572112219	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9308338	GGTCCTGCATACCCA[A/G]CAGTAGGTCCTGCAT	80176
rs572197234	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9338264	GCCAAGGCCCTGGCC[A/G]TGGGCTCCCCAGGAC	80176
rs572216987	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9302249	ATTGATTTTGGATGT[C/T]AACTTGACTAGATTA	80176
rs572220371	snp	C/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9302424	TGTTTTTGGAGGACA[C/T]TGGCAATTGAGTCAC	80176
rs572255636	in-del	-/CTTA	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9300811	CAAAGGCCCATGGTT[-/CTTA]CTTTGCCCACTGCCT	80176
rs572281306	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9316977	CCAGGCCCCGTAGCA[A/G]GGCCAGGCCTCACCT	80176
rs572298054	snp	A/G	0.00318978	0.0398085	intron-variant	SPSB1	GRCh38.p7	1:9316697	CCGGATTCCTGTGGC[A/G]CGGCACGGGCCTTCG	80176
rs572393031	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9318023	TGGTGACGTGCCAGG[C/T]GGGGAGAGGAAGCAG	80176
rs572474896	snp	A/G	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9310153	GCCTCTGCACCTGCC[A/G]TGGGAAGGCCACAGA	80176
rs572477458	snp	C/G	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9313018	GCACTGTTCTGGGCA[C/G]TTTCCACACATTAAC	80176
rs572499242	snp	A/G	0.00318978	0.0398085	intron-variant	SPSB1	GRCh38.p7	1:9319011	GCGAAACCTGTCTCT[A/G]CTAAAAATACAAAAA	80176
rs572514995	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9305969	GGAGGGCCCACAGAC[C/T]TGGGGACATTTGTGC	80176
rs572544392	snp	C/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9344063	AAAGTGCTGGGATTA[C/T]AGGCGTGAGCCACCG	80176
rs572565124	in-del	-/C	0.401215	0.199083	intron-variant	SPSB1	GRCh38.p7	1:9361155	TGGATCTGTCATTTT[-/C]CTTTTTTTTTTTTTT	80176
rs572571208	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9317918	CCTTGGCACACCATT[C/T]GCTCCGCGAGTTTGT	80176
rs572610395	snp	G/T	0.000798403	0.0199641	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291388	TGACGGGTTTCATCG[G/T]GTTAGCCAGGATGGT	80176
rs572619766	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9310288	CTTCAAGCAAACTCA[A/G]GATTCACAGGATTCA	80176
rs572725130	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9335730	ACTTGAGCACTTGAG[C/T]CCAGAAGGTTGAGCC	80176
rs572758763	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9294804	AGGAAGGGGATGGGG[A/G]CCTCTCCCTTCTGCC	80176
rs572772311	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9361303	CCACCATGCCCAGCC[A/G]GATCTGTTTTCTTGG	80176
rs572772550	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9322070	TATGTGCACTCCCCG[A/G]GCACCCATCCTGCAA	80176
rs572786762	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9322565	TGAGGGCTCAGGGTT[C/T]GTAGCTGATGAGTTT	80176
rs572791759	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9323330	AGCCCCTTGGCGGGG[C/T]GCTCAGCAGTGGATG	80176
rs572828535	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9362494	ATGTCCTGGAGCGTG[G/T]TCCCCACAAGCTGCT	80176
rs572845834	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9315103	TTGTGGGATGAATCT[C/T]CCCTCTCTGTAGAGG	80176
rs572862883	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9347067	TCACACCTGTTATCC[A/G]AGCACTTTGGGTGGC	80176
rs572871288	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9321353	AGCTCTAGACAGCCC[A/G]ATGGCAGGGGGTGGG	80176
rs572874062	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9320476	CCTCTCGAGGGCTGG[A/G]AGAAGCCGTTTCCCT	80176
rs572925230	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9315591	GCACACTCTGAGGCC[C/T]ACAGTGACATGTGCA	80176
rs572949780	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9346658	TGCAGTCTGGCCTGT[C/G]TCAGCCTCCCCCAGG	80176
rs572982459	in-del	-/CGAA			intron-variant	SPSB1	GRCh38.p7	1:9298407	GAATGAATGAGTGAA[-/CGAA]TGAATGAATAAGTGA	80176
rs572995030	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9325930	GCAGGAGCTTGGCAG[C/G]TACCAGGAACAGCCA	80176
rs573009094	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9326292	CTGGGCAGGTTGCTT[C/T]TCTGATCCTCAGTCT	80176
rs573099250	snp	A/G	0.00199481	0.0315187	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9368504	TTCCCCTGTGTCTCC[A/G]GGTAACCAGCTAACT	80176
rs573110507	snp	A/G	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9316466	ACTGGTACTCAGCAA[A/G]CAGAGCAGACTTTGA	80176
rs573163434	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9366418	GTGGGGCCAGCCAGG[A/C]CTGTCACGTATGATT	80176
rs573166985	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9330285	CCAGCCTGGGCAACA[C/T]GGTGAAACCCCGTCT	80176
rs573169342	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9324423	TGATGAGCGTGGGGG[C/T]GTCTGGTGCCTGGGT	80176
rs573179644	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9324840	CGTGTTTGCGACAAG[C/T]CTGTTCGCCTGGCCG	80176
rs573181141	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9359102	GCCACTCAGAGCATC[A/G]CAGCCGGGCGCTATT	80176
rs573199285	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9353799	GGTGGGCGCCTGTAA[C/T]CCCAGCTACTTGAGA	80176
rs573220709	snp	C/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9330899	CAAGGGTTCCGGTTT[C/T]TCCACATCCTTGCCA	80176
rs573245362	snp	C/G	0.00318978	0.0398085	intron-variant	SPSB1	GRCh38.p7	1:9306300	GCTCTGTGGTTTCCA[C/G]CACGGAGAGCATTTG	80176
rs573259034	snp	A/G	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9321768	TGAGTCGGTGGAGGA[A/G]GAGGACTCTGAGAGG	80176
rs573264379	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9320935	CCTCCCCCTGCCAGG[C/T]TCCAGTGGAAGGTCC	80176
rs573342893	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9295696	CCCCCATGGTGTGTG[C/T]CGTGCTCCCTTCCTG	80176
rs573363958	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9312932	GTGTCCCCTGCAGAC[A/G]CACCTTTTCCTTCTG	80176
rs573368838	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9301516	CCAAACAAAAAAGCA[A/G]TTGGGGGAAGATGTA	80176
rs573403010	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9313639	AAGCCTTAGCCAGGC[A/G]AAGGAGAGGGCATGG	80176
rs573403445	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9364287	AGAGAACACACCTGC[A/G]AATTCCCCACTCCTC	80176
rs573408097	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9296125	AGAGTGCTTTATGGA[C/T]GTGACTTTGTTTGAA	80176
rs573414769	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9336946	TGCCTGCTGGTCCCC[A/G]CTGAGGGGCCGCTTC	80176
rs573428021	snp	C/T	0.00398564	0.0444627	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9368596	GTGGGTTTGATTTTG[C/T]TTTTGCTTTTCTAGC	80176
rs573501451	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9337528	TGAGGCTGGGGGTAG[A/G]GGAGGGGTGCACCCT	80176
rs573504025	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9300975	GAAAGTGGACAGCTG[A/C]AGCACTATAGCCCCT	80176
rs573567236	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9357843	GGCTCACCCCGTGTA[C/T]GGCCCTCTCTCAGAG	80176
rs573623462	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9368163	CCCATCCTGGCTGCC[G/T]GTGCCCCGTACCCTG	80176
rs573624414	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9358825	TGTATCATAGCTCCA[A/G]TACAGTACACAGACC	80176
rs573644299	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9310207	GCTCCTGCACCTGCC[A/G]TGGGAAGGCCACAGA	80176
rs573650871	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9316994	GCCAGGCCTCACCTT[A/G]GATGCACCTTCCTGC	80176
rs573706979	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9310568	GATGTGATGGTGCAT[A/G]CCTGTGATCCCAGCT	80176
rs573707702	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9315713	AGAACACTGAGTGGG[A/G]AGTTGGTGGGGGGCC	80176
rs573725759	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9342977	GCCTCTCTCTGCCCT[C/G]CACCCCCATCCACAC	80176
rs573725855	snp	C/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9337567	ACCCCAGCCCTCTGC[C/G]GGCTTTTCTCCCCTT	80176
rs573736299	snp	A/C	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9352344	CCATCCGGATAATGC[A/C]TGCTACAGCCCCACA	80176
rs573795270	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9347351	AGTGTGTGAAATCAT[C/T]GTTTCTCAGCCTTTG	80176
rs573795489	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9321417	CGGATCCTGTGTGAT[G/T]TTACGGAACTTGTCC	80176
rs573808081	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9321782	AGGAGGACTCTGAGA[C/G]GCTGGGAGACTGGCC	80176
rs573823133	snp	C/T	0.00358779	0.0422022	intron-variant	SPSB1	GRCh38.p7	1:9352919	TGACAGACGAGATCC[C/T]GGGAGAAAGGTCCTC	80176
rs573853296	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9320846	AGCTACAACGTCCTG[C/T]GCCGGGTTTAGCAGG	80176
rs573942064	in-del	-/AAA	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9343967	ATTTTTTGTATTTTT[-/AAA]AGTAGAGATGGGGTT	80176
rs573956728	in-del	-/A/AAA	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9332188	GACCCCACCTCTACC[-/A/AAA]AAAAAAAAAAAAAAA	80176
rs573984539	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9363397	CCTAACTGGTTTATT[C/T]AGTGAGATCCAGAGA	80176
rs573994202	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9320549	GTGGCCTCGCTCCGT[A/G]CATCTAAGTTGTTCC	80176
rs574038889	snp	A/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9301857	CACCTGGTGGAAGGC[A/T]CATTGGACCACTTCT	80176
rs574097186	in-del	-/T	0.00318978	0.0398085	intron-variant	SPSB1	GRCh38.p7	1:9367350	CTTTACTGATTTGAG[-/T]TGAATACTAATCAGT	80176
rs574152415	snp	A/C	0.00358779	0.0422022	intron-variant	SPSB1	GRCh38.p7	1:9359613	AGGCTGAGGCAGGAG[A/C]ATTGCTTGAACCCGG	80176
rs574192708	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9323762	TACAGGCCTCAGTGA[G/T]ACAGTGCTATGTCAT	80176
rs574202846	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9324225	AGCTGGAATGGGCCT[A/G]GGTGGGAGGGACTTT	80176
rs574289429	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9296188	ATGGTTTCACGGTGC[A/G]TGCGAGTACTGGCTC	80176
rs574306930	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9369240	GGACCTTACCTGTAA[A/G]ACTTTTAAAGATTTT	80176
rs574346346	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9356692	AGAGTGTTTTGAAGA[C/T]GATATTCCAGTGTAT	80176
rs574381898	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9349474	GAGAGGCCAAGGGAC[A/G]TGGAGCGTGAGAGGC	80176
rs574433061	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9304217	ATACCATTGGTCCCC[A/G]GGGTCTTTGGCCCGG	80176
rs574486739	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9362565	GACATTGCGGAAGCC[A/G]GGGCATTCTCTGATG	80176
rs574582136	snp	G/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9328943	TTGCCAAATCTCCCA[G/T]GGTACGCTGGGGTGA	80176
rs574615914	snp	A/G	0.00318978	0.0398085	intron-variant	SPSB1	GRCh38.p7	1:9362133	CAGCTGGACTCTGCC[A/G]GGAGCTACTCATCGG	80176
rs574659900	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9314131	CAGTGAGCTGAGATC[A/G]CACTACTGCACTCCA	80176
rs574663622	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9301719	GGTGATGCATGGGCT[C/T]AGCAGCATGGACTGC	80176
rs574667631	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9334877	ATGTATCAAAATGTC[A/C]TTCCGTGTTAAGGCT	80176
rs574679397	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9366441	GTATGATTCAGGACA[G/T]GGTTTGCCATGTCTT	80176
rs574680524	snp	C/T	0.0103295	0.0711199	intron-variant	SPSB1	GRCh38.p7	1:9354142	CTGCAGAGCCTGGCC[C/T]TGGCTGGCCCCATAC	80176
rs574700615	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9328438	ACTCTCTAGGAGGGG[A/G]TATGATGTTTCCTAA	80176
rs574717298	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9299176	AGCTGTTGATCTGAC[C/G]AATGCCCTTCTCTTT	80176
rs574718117	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9294912	CACTGAGGAATTTTG[A/G]AGTCAGGGAAGTCCT	80176
rs574742007	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9340204	AGACAGACTCTCCTT[A/G]GGCAGGCTTTCTCTC	80176
rs574746070	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9317057	TCCTTAACCTGGCCT[A/G]TGAGGGTTTGCTTCC	80176
rs574762639	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9346065	GGGAGCACAGAACCC[C/T]AGTGAGCGGGCAGAG	80176
rs574769910	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9368020	AGGTGCTTAGACAAG[A/G]GCTGGTGCCCGGCCC	80176
rs574790373	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9295612	AATCATCACAGATGT[G/T]GAATTTCTTCACCAG	80176
rs574818177	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9366046	GAGATCTGAAGCTGA[C/T]GGCTCATCTGAGATG	80176
rs574853354	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9299155	CTGGTCCCTGCTACT[A/G]CATGCAGCTGTTGAT	80176
rs574858842	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9300699	ACCAGACATTGGGCA[C/T]GTGTGGCAGAACGCT	80176
rs574865317	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9300619	TTGACCATCAGCCAC[C/G]AAGTTGCCATGTGAC	80176
rs574920622	snp	G/T	0.00318978	0.0398085	intron-variant	SPSB1	GRCh38.p7	1:9324940	GAGCAGGGACACCCG[G/T]CCTGGCGGGCTGGTG	80176
rs574971444	snp	C/T	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9319622	CGGTGGCTGATGTTC[C/T]GTACCGGGCTGGTAT	80176
rs575022759	snp	C/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9314262	ACATTTTCAGTGTCT[C/G]TGCTGGGCCGGGAGT	80176
rs575054237	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9322061	TGATGTAAATATGTG[C/T]ACTCCCCGAGCACCC	80176
rs575106048	snp	A/G	0.0023933	0.0345097	intron-variant	SPSB1	GRCh38.p7	1:9314953	CTTACCTGAGGGAGT[A/G]GAGTCCTTGGCACTG	80176
rs575142286	snp	C/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9309583	CACAGTGGCTCACGC[C/T]TGTAATCTCAGCACT	80176
rs575182079	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9341560	GAACATTGCCAGACC[A/G]TCTCTCTGGTTGGGT	80176
rs575221149	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9357902	GCCTGCAAGTCCCAC[A/G]TTGGGAAGCAAGTGG	80176
rs575274994	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9324782	CTCTGACAAAAACGC[C/T]TGTGGCCCTGGACTT	80176
rs575308486	snp	A/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9324276	CCGGCACATAGTGGG[A/T]CTCACAGCTCTTCAT	80176
rs575322299	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9330866	GCTGTGCCATTTTGC[A/G]TTTCCATCAGTGATA	80176
rs575343211	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9362219	TCCTTCCATGTCGGG[A/G]AGGGGTTGTCCCAGA	80176
rs575383525	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9295375	CCAGTGGCTCAGACA[G/T]CCCCGAGCAGGGAGC	80176
rs575515191	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9320586	CACAGAGGAAGCACG[C/T]AGCCCTCTCTTCCAT	80176
rs575558879	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9325768	CAAAGGACGTTTGCC[A/G]TTTGGGCAGGATGGC	80176
rs575593392	snp	A/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9363703	CTGCAGTTTTAGAAA[A/T]TTTTTTTTTTTTTGG	80176
rs575595505	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9358348	TCTGTGCAGCCTGGC[A/G]CCCCCAGGTCATGGG	80176
rs575644720	snp	A/G	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9350699	GGCAGTACGAGCCAC[A/G]CCCTTTGCGTCTGCT	80176
rs575662670	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9328143	CCACACACCTTTACA[C/T]CCCCTCCTATAGAGC	80176
rs575663847	snp	A/G	0.00279162	0.0372561	intron-variant	SPSB1	GRCh38.p7	1:9328342	TTTTCTTCAAGTTTG[A/G]GAACTGCTAGAGTTC	80176
rs575667338	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9328140	CTGCCACACACCTTT[A/G]CACCCCCTCCTATAG	80176
rs575735016	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9334108	ATTTATTCTTTGAGG[C/T]AGAGTCTTGCTCTGT	80176
rs575758896	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9305907	GTGGCCAGGTTGGAA[A/G]GGCGGGAAGGGTGCC	80176
rs575803226	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9326900	AAGGGAGCAGCTGGC[A/G]CCTTTTTTAGGTGGA	80176
rs575845555	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9346999	GCCCCAAAGCTTCCC[C/T]AGGATTCTCATCCTT	80176
rs575911458	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9328289	AACTGTCATCCCTCA[C/T]GATGTTGTGCAAAGA	80176
rs575911832	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9300850	CTCCAGCCTGTATCT[A/G]TGGTCTCCTGGGGAG	80176
rs575912268	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9342263	CCTGGGCTGTGCCAG[C/G]CCTGTGAGTGACGAT	80176
rs575934517	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9368100	AAACTCACCATGGAC[C/T]CCAAGGCAGAAACCA	80176
rs575945538	snp	A/C	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9365973	GCGAAGCGGGCGAGC[A/C]GGGCCGCGCAGCCTT	80176
rs575973196	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291589	TTATTATTATTATTA[C/T]TTAATTTTTGTGCAG	80176
rs576082901	snp	A/C	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9299028	TGGTGACCCCCACCA[A/C]ATCCCCATTCAACTC	80176
rs576122150	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9307433	CCTGGGAACCAATCT[A/G]TATTCTGATTTGACG	80176
rs576123164	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9365436	CCCTCTTCTTTTAAA[G/T]CTTGGGGTTTAGTAA	80176
rs576172707	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9354511	CTCTCTTGAACGAGG[C/T]TCAAATCTTCTGCTG	80176
rs576201192	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9336368	AGTAGCTGGGATTAC[A/G]GGCACGCACCACTAT	80176
rs576207850	snp	A/C	1.7219e-05	0.00293414	synonymous-codon	SPSB1	GRCh38.p7	1:9355934	AAGACTGTGGACATG[A/C]GGGACCCCACGTACA	80176
rs576212473	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9349251	TCCTGCCTGCATCCC[A/G]TTTTTCGCTCCTCTC	80176
rs576275733	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9311585	CTTGAACCAACGCTT[C/G]AGCCAGAGCAGTCTC	80176
rs576310520	snp	G/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9307132	GGGGTTTCACCATGT[G/T]GGCCAGGCCGGTCTC	80176
rs576414245	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9359203	TGGGCCCTGGGCCAC[A/G]TGGTCAGTTGACTTT	80176
rs576457460	snp	A/G			utr-variant-3-prime	SPSB1	GRCh38.p7	1:9369058	TACATACATATATAT[A/G]TATTTGTCTGTAAGA	80176
rs576521102	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9328398	CGGGACTTCTCAGAG[C/G]CTTTAAGATGCTGAT	80176
rs576524369	snp	A/G			utr-variant-3-prime	SPSB1	GRCh38.p7	1:9368341	GGCACATGTGCACAC[A/G]TGCCCAGGCACAAGT	80176
rs576530841	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9334948	TTTGTTCATCTGTCC[A/G]TGGACGCGGGTTGCT	80176
rs576535932	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9340681	TGCTGTGATGTGGCC[A/G]GCCTTCCCTGCCACC	80176
rs576536517	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9328813	TGTTGACATAGGGCA[A/G]GGGAATTGTTGATGT	80176
rs576558731	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9349717	TCTTCCGTGACTCAC[A/G]GCCTCTGGGCCAGTT	80176
rs576562886	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9314077	GCTACCTGGGAGGCT[A/G]AGGCAGGAGAATTGC	80176
rs576656833	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9334154	GCGGTGGTGCGATCT[C/T]GGCTCGTTGCAACTT	80176
rs576660099	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9313125	GTCAAGTCCGGGCGC[A/G]GTGGCTCATGCCAGT	80176
rs576684496	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9318834	CAGTCACATGAGCTG[A/G]TGATTGTAACACAGG	80176
rs576730791	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9323670	ACATGGCTGCCCGCG[C/T]GTCTCCAGGCACCGA	80176
rs576740176	snp	G/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9318503	ACTCCCAGGTTTCCA[G/T]CATCCAAGGAAGACC	80176
rs576742651	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9333651	GTCAGCTTCCTGAAG[C/T]GCCTGCGGTGTGAGC	80176
rs576851342	snp	C/G	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9294292	TCTCTGTGTCTGTGT[C/G]TCTGAGTGCGTCTGT	80176
rs576903620	snp	A/T	0.00597247	0.0543191	upstream-variant-2KB	SPSB1	GRCh38.p7	1:9292776	CCCTGCAGTGCTGAG[A/T]GGTCCGTGCGCCCGA	80176
rs576950030	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9299413	GGAGGCCGAGGCAGG[A/G]GGATCGCTTGAACTT	80176
rs576956898	in-del	-/GT			intron-variant	SPSB1	GRCh38.p7	1:9348964	TGTGTGTGTGTGTGT[-/GT]ATATGTGCGTGTGTG	80176
rs576988060	snp	G/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9299100	TGATAGTGGATTATT[G/T]TAAACTTAACCAAGT	80176
rs577007072	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9345198	TGATCCACCCTGCCT[C/T]AAGCCCCCGTCTCCT	80176
rs577008988	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9350972	GTCCAGTGTTAACAG[A/G]AGCCATCCAGGCACC	80176
rs577017857	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9344385	ACAGGGCCTTTCCAT[C/G]TGCCTTTCCTCACCG	80176
rs577020565	snp	G/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9339369	GGGCTGTGACTCACC[G/T]CCAGGCCAGGTTCTG	80176
rs577049687	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9310457	CAGCACTTTGGGAGG[A/C]CGAGGCAGGCAGATC	80176
rs577078327	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9339710	GGCCTCCAGCAGGGT[C/T]GCCCTGACCTCTGTC	80176
rs577087225	snp	A/G	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9347995	TGACGCCCAGGTTCG[A/G]GTGCAGTGGTGCGAT	80176
rs577096604	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9350278	CCTGAGGGCTGCGGA[C/G]AGGAGAACTGTCATT	80176
rs577118541	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9302895	ATCATATCCCCTAGG[A/G]ACCCGCTAGCGAAAT	80176
rs577127373	snp	A/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9365987	CAGGGCCGCGCAGCC[A/T]TCCAACGCTCAGAAG	80176
rs577150004	snp	A/T	0.00874735	0.0655527	intron-variant	SPSB1	GRCh38.p7	1:9299811	ATTTTTTTTTTTTTT[A/T]AATTAGCCAGGCATG	80176
rs577171248	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9369369	TGACCCTCTAGCTCT[C/T]TCTGCATCTCCCACC	80176
rs577171740	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9357713	AGGGGAGTGGCCTTT[C/T]TCAGACTGTGAATGC	80176
rs577192945	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9300207	AAGAATAAGTTGTTA[C/T]AGCTTTCCTCCTGCA	80176
rs577226802	snp	A/C	0.00199481	0.0315187	intron-variant	SPSB1	GRCh38.p7	1:9340775	TTTTTTATTTTATGG[A/C]AAGTCCAGCTTGCAG	80176
rs577230353	snp	A/G	0.00517822	0.0506191	intron-variant	SPSB1	GRCh38.p7	1:9343999	TTCACCGTGTTAGCC[A/G]GGATGGTCTCGATCT	80176
rs577254773	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9316636	CCTTAGAGCCCACCC[A/G]TTCCCGCCATCTTGG	80176
rs577279222	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9336079	TGAGGCTCTCTGCAG[G/T]CTTCCAGGGTAGGCA	80176
rs577288519	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9335643	CCATCTCTACAAAAA[C/G]TAAAAAACTAGCTGA	80176
rs577291000	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9332182	ATAGTGAGACCCCAC[C/G]TCTACCAAAAAAAAA	80176
rs577327275	snp	C/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9330577	CTTGTGATCTGGACA[C/T]ACGTATCCCTAACTT	80176
rs577343232	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9329700	CTCATTTCAAAAACA[A/G]CAACAAAAAAAAAAA	80176
rs577374846	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9304422	ATCCTATGGGTTTTG[C/G]ATCTCTGGAGAATCC	80176
rs577393804	snp	C/T	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9353540	GCTGCAGAGGGGACA[C/T]CTCAGCTCTGTAATG	80176
rs577403446	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9296668	GAAGCAAATACAAGA[C/T]GTCAGGTCATCTGTA	80176
rs577478025	snp	A/G	0.000798403	0.0199641	intron-variant	SPSB1	GRCh38.p7	1:9353031	AGTAATTCCTGCCCC[A/G]TCCTCCCAGGGAGCT	80176
rs577517243	snp	C/T	0.00159617	0.0282053	intron-variant	SPSB1	GRCh38.p7	1:9359061	TCAGGATTCGGGAAC[C/T]GCATCTGTGAGCTGG	80176
rs577551626	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9301902	AGCGTTTTGTCCTTA[C/T]TGGAGCAGGCACTTA	80176
rs577553563	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9309420	ACTCCTGGGCTCAAG[C/T]GATCTTCCCACCTCA	80176
rs577578598	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9364442	ATGGGGAAACAAGTC[C/T]GGGCAGACGGAGGGA	80176
rs577618802	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9343145	GGCATTGAGTACATT[C/T]GCAATATAGTATACT	80176
rs577626558	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9307576	GGAAGCTGGATTTCC[C/T]GTCCTGGCTCAGTTG	80176
rs577644236	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9313806	TGCTCAGTGAAGGCT[A/G]AGTGAATGGAGGAGT	80176
rs577684668	snp	G/T	0.00318978	0.0398085	intron-variant	SPSB1	GRCh38.p7	1:9338182	GGAGGTTGGCGGTTG[G/T]GGGGTGCCACTCAGC	80176
rs577713993	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9307121	TTAGTAGAGATGGGG[C/T]TTCACCATGTTGGCC	80176
rs577743907	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9332421	TGAATCTGGGTGAAC[C/T]AGAGGTTGATGATAG	80176
rs577749588	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9311661	TAGAAGATTTAACTC[C/T]CGCTGCTTCTGGCAA	80176
rs577800763	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9342664	GGGGTCATCCCCTCC[C/T]CAGACCACAGTTTGG	80176
rs577884262	snp	C/T	0.00478085	0.0486577	intron-variant	SPSB1	GRCh38.p7	1:9310688	CAATGGGAGTTAGAC[C/T]TTGTCTTAAAAAAAA	80176
rs577923323	snp	A/G	0	0	intron-variant	SPSB1	GRCh38.p7	1:9311092	CCTCTAGCCTCCCAG[A/G]CTCCCTGAAAGCCAA	80176
rs577930393	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9324339	GGTGGTGTGCCATCT[A/G]CGGCTCTGCTCTGGT	80176
rs578000371	snp	C/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9343997	GTTTCACCGTGTTAG[C/G]CAGGATGGTCTCGAT	80176
rs578032393	snp	A/G/T	0.00119737	0.0244387	intron-variant	SPSB1	GRCh38.p7	1:9317028	CAAGTGGAAACACAC[A/G/T]GTGGAATTTAGAATC	80176
rs578098751	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9345564	CATCAGGCACAGTCC[A/G]TTGTCCTCGCCACCC	80176
rs578114880	snp	C/T	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9359696	AACAGAGCAAGACTC[C/T]GTCTCTGGGAAAAAA	80176
rs578119064	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9360388	TGGGTCAGGGGGCAC[A/G]GGAGGAGCCTGATGG	80176
rs578144784	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9365635	TATACCCATAAGCAG[A/C]CTCTCTCCATTCTGC	80176
rs578247833	snp	A/G	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9326385	GGAGTCTCTGAAGGG[A/G]CCACAGAAAAGTCAG	80176
rs578248486	snp	A/C	0.000399281	0.0141238	intron-variant	SPSB1	GRCh38.p7	1:9332927	GAAGTGTGGTGGCAG[A/C]AGGAGAGGGCATCGG	80176
rs745342021	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9361991	GCAGTTCAGCATTTT[C/T]GAATTTTCTTTAACG	80176
rs745407605	snp	G/T	3.52902e-05	0.00420046	synonymous-codon	SPSB1	GRCh38.p7	1:9356167	CAGGGGCAAAGTCGG[G/T]TATACCCGTGGGCTG	80176
rs745428385	snp	C/T			upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291527	TCCACCTGCCTCAGC[C/T]TCCCAAAGCGCTGGG	80176
rs745462242	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9337069	CCAAATGCTCCTGGC[A/G]TTCTAAGAAACTCCT	80176
rs745468790	snp	A/G	6.97532e-05	0.00590523	missense	SPSB1	GRCh38.p7	1:9356231	CGGGGCACACACGCC[A/G]TGGTGGGGGTGGCGA	80176
rs745550599	snp	C/G			downstream-variant-500B	SPSB1	GRCh38.p7	1:9369942	CTAGGGGAAGGAGCA[C/G]GTCCTTCATTCGTCT	80176
rs745576254	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9336008	TCCAGCACTGTTTGA[C/G]GACCTAGTGTGTGCT	80176
rs745581730	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9360689	GTATGTGTCTCTCCG[C/T]GGCCCCTCCTCTTCT	80176
rs745621805	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9301581	AGACCTCCCGAGTGC[A/G]CACAGGACATGAGGT	80176
rs745638586	snp	A/G	8.28205e-05	0.00643455	synonymous-codon	SPSB1	GRCh38.p7	1:9356290	GTACACAACCCTCGT[A/G]GGGAATAACCACGAG	80176
rs745779011	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9331534	ACGGGGTTTCATCAT[A/G]TTGACCAGGCTGGTC	80176
rs745804744	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9365117	CGGCCTCGGCCTCCC[A/G]AAGTGCTGGGATTAC	80176
rs745863808	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9340140	CCGGGTGCAGGGCAC[A/G]CAGGGTGACCAGTTC	80176
rs745901037	snp	A/C/T			intron-variant	SPSB1	GRCh38.p7	1:9307088	ACGTGCCACCACGCC[A/C/T]GGCTAATTTTTGTAT	80176
rs745902000	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9326800	CATTCCTGCAGTTTA[G/T]TCTGTGTTGGTTTAA	80176
rs745982728	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9325514	GCCCTGCTTCTATGG[A/G]AGCGGCATTTCTGCA	80176
rs746020012	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9346935	TGAAACAGTATAATC[A/G]GAAGTCTTGGGATAG	80176
rs746060508	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9325381	TGAATGAGGGGCCTG[A/G]AAGGCAGACCTGGGG	80176
rs746062295	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9358331	GGGCTGCTTGGTCCT[C/T]GTCTGTGCAGCCTGG	80176
rs746070666	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9324340	GTGGTGTGCCATCTG[C/T]GGCTCTGCTCTGGTG	80176
rs746157194	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9333434	CTCCCAGGTTCAGGC[A/G]ATTCTTCTGCCTCAG	80176
rs746242884	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9332506	TATGAGTGGGAGCAG[A/G]GTCACTGCTGGGGAG	80176
rs746263749	snp	C/G	1.71328e-05	0.00292679	missense	SPSB1	GRCh38.p7	1:9367527	CCTGGGGGAGATCCA[C/G]ACGCTGCCGCTGCCG	80176
rs746292750	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9352024	CCTCCCAGGCCCTCC[C/T]TCCCACAGACTCCCA	80176
rs746299293	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9338775	TGAAACGTGGGTGGC[A/G]TGGGCCACGATTCTG	80176
rs746342309	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9309757	TGAGGCAGGAGAATC[A/G]CTTGAACCCAGGAGG	80176
rs746342692	snp	C/G	9.55825e-05	0.00691246	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9367592	GTTCGCCATCATACC[C/G]CCAGCGCGACAGCCA	80176
rs746365505	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9311995	CGTTTTTGTCTTGGT[A/G]TAACCGTTGGCCCTG	80176
rs746445035	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9328262	AGCCCAAAGACATTC[A/G]GAGGTCCTCCAAACT	80176
rs746445960	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9311076	ATCCTTTCTTCTCCC[A/G]CCTCTAGCCTCCCAG	80176
rs746533599	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9319776	GTCGGCCTGGGGTGG[C/T]GGGGTGACTGGTTCC	80176
rs746599086	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9362897	CAGAAATTATTTAAA[A/T]GAATGAGCGCCTAAG	80176
rs746606697	in-del	-/A			intron-variant	SPSB1	GRCh38.p7	1:9331176	TAATTGCTGTGTAAC[-/A]AACGGTTCATGGTGC	80176
rs746626758	snp	A/G	1.65485e-05	0.00287645	missense	SPSB1	GRCh38.p7	1:9356066	CATTCATGGAACAAC[A/G]ACGACCGATCGCTCA	80176
rs746629302	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9332452	AAATTGGCAGCATTG[C/T]AGAGGCCAGGAGGGG	80176
rs746669842	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9294428	GGTACTGCTCCTCAT[A/G]GTGATTTCTTTACTT	80176
rs746687978	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9362216	CCTTCCTTCCATGTC[A/G]GGGAGGGGTTGTCCC	80176
rs746705710	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9295656	GGTGGGGGCCTAGCC[C/T]GTGGAAGCCAGCGCT	80176
rs746717582	in-del	-/T			intron-variant	SPSB1	GRCh38.p7	1:9311162	CGCAGGATAAAGGGT[-/T]TTTTTTTTTTTTTTT	80176
rs746756350	in-del	-/GTGTGTGC			intron-variant	SPSB1	GRCh38.p7	1:9295236	TGTGTGTGTGTGTGT[-/GTGTGTGC]GCGCGTGCGGTTGGG	80176
rs746830582	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9315768	ACGGAGGGACCGCAC[G/T]GCTCACAAGGTTGCT	80176
rs746842022	snp	A/G	1.75718e-05	0.00296405	synonymous-codon	SPSB1	GRCh38.p7	1:9356572	CCGAATGCGCTACTT[A/G]AACGGACTCGATCGT	80176
rs746850434	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9327138	AGTGCCCACTTGCAG[C/T]GCTTCCGGGGGTCCC	80176
rs746883468	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9345525	TGTGTCCCTGGGGTC[A/C]CTCAAGAACTGGCTT	80176
rs746918644	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9323081	GGCCAGGCGGCCGCC[C/T]CTCCCCAGCTCCGGC	80176
rs746949566	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9304126	CTGGCTCTCTGTCCC[C/G]GAGCTGGGACATCCT	80176
rs746955014	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9305580	CGATGTGGGCCCAGG[G/T]TGTGGGTGCTGGGGG	80176
rs747008619	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9322295	TAGCCTCGGTTTGCA[C/G]GTGGGGAAACTGAGG	80176
rs747017883	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9353064	CCTCTGTGCCCACAG[A/G]ACCCTGCAAAATTGA	80176
rs747033695	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9308303	CCTGGGCCCATCCTT[G/T]GTGGGGTCATGGATA	80176
rs747042234	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9297793	TCATGTAGAGTTAGG[C/G]ATTCAAAGGCTTAGG	80176
rs747100306	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9339191	TCTCCCCCCAGCGGT[A/G]AGGACCTGTGGGGCT	80176
rs747103093	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9298657	CTGATACTGATTCCA[A/G]GAAACCAAAAATATC	80176
rs747109744	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9364464	ACGGAGGGATGTGCT[A/C]CAGGTCAGGCTGCGG	80176
rs747112283	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9356674	AGTTGATTCATTGGA[A/G]CTAGAGTGTTTTGAA	80176
rs747123238	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9317746	CCTTGGCCTCCCAGA[C/G]TGTTGGGATTACAGG	80176
rs747245123	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9347808	ATTGCTGGGCGTTTT[A/G]CACATGGACAGGGAC	80176
rs747304455	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9358605	CTCAGCCCTGCCTCC[C/T]TCCTCCCAGCCATGG	80176
rs747325273	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9340304	GAAGGCAGGGACACT[A/G]GTGTTTGGGGACTGG	80176
rs747342302	snp	A/G			downstream-variant-500B	SPSB1	GRCh38.p7	1:9370029	CTTGTTCTGCTAGCC[A/G]TGTGGGCAGAGCCCC	80176
rs747472455	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9342989	CCTGCACCCCCATCC[A/G]CACCCACCCCCTGTC	80176
rs747484754	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9338918	GTGGACACCCTGGCC[C/G]CATTCTGGAGGACTC	80176
rs747505621	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9333620	ACAAGCGTGAGCCAC[C/T]ATGCCCGCCCTCCTT	80176
rs747547765	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9362906	TTTAAATGAATGAGC[A/G]CCTAAGCTTCCTGGG	80176
rs747575556	in-del	-/TCAC			intron-variant	SPSB1	GRCh38.p7	1:9325571	CCGTGGAACAGACAG[-/TCAC]TCAGCAGGCATGTAT	80176
rs747602337	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9313156	AATCCCAGCACTTTG[G/T]GAGGCTGAGGCGGGT	80176
rs747602790	snp	C/T			utr-variant-3-prime	SPSB1	GRCh38.p7	1:9368682	ACTAAGAAGGGAGGG[C/T]GAGTGGGTCTCCATT	80176
rs747608083	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9320551	GGCCTCGCTCCGTGC[A/G]TCTAAGTTGTTCCTT	80176
rs747645784	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9312442	GGTATTATGCACACG[C/T]CACGCAGTTCGCCTA	80176
rs747669882	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9320720	CACCCCGGGCTCGCC[C/T]CTCTCGGCTCTGGCT	80176
rs747766382	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9342442	ACCGTGGGAGAGCAC[A/G]GAGGATCCCAGTGGC	80176
rs747771989	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9364235	AGACCCCTTGGCCCT[C/G]ATGCAGGCCAGATGC	80176
rs747775521	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9318567	TGGACAAGTTACTCA[A/G]CCTCTTTGAGCCTTG	80176
rs747786718	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9297394	AAGGGCTTGACGGGT[A/G]CCCCAGTTGTGAACA	80176
rs747803528	in-del	-/TT			intron-variant	SPSB1	GRCh38.p7	1:9317839	GGCGAGGGAACCAAT[-/TT]TTTTTTTTTTTTTTT	80176
rs747812281	snp	C/T	1.73312e-05	0.00294369	synonymous-codon	SPSB1	GRCh38.p7	1:9355930	GATCAAGACTGTGGA[C/T]ATGAGGGACCCCACG	80176
rs747889225	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9352386	TAAGTGGAGACGATG[A/C]AGGGCCCTGTCTAAG	80176
rs748172023	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9315966	CGGGCATCCTGGTGC[A/G]GTTCTGCAGCCAGCG	80176
rs748203989	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9365836	GAGACCGTGGATGAA[A/G]CCTCAGATCCATTAG	80176
rs748216174	snp	C/T	1.66466e-05	0.00288496	intron-variant	SPSB1	GRCh38.p7	1:9367442	GCAGTTTCTCTGTCT[C/T]CCCAGCCGAGCCGCT	80176
rs748235287	in-del	AGACGGAGTCTCGCTCTGTCACCT/GGGGGGGTCCCCCCTCCCCCCCCGGGC			upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291205	TTTTTTTTTTTTGTG[lengthTooLong]GGGCTGGAGTGCAGT	80176
rs748245543	snp	A/G	1.82543e-05	0.00302107	intron-variant	SPSB1	GRCh38.p7	1:9356604	AGTGTCTCCTCTGCT[A/G]TCAGAGGCAATGCCC	80176
rs748317458	in-del	-/CT			intron-variant	SPSB1	GRCh38.p7	1:9311333	GTTTCTTTCTTCCCC[-/CT]GATGGGTCTCGGCGT	80176
rs748331113	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9365174	TTTTCATTTTTGAGA[C/T]AAGGTCTCTGTTACG	80176
rs748432036	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9349839	CTTACTTGTGGGAAA[A/G]TGTTGCTAGGAGTTC	80176
rs748459359	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9315013	ACTTTTTAAGATGTT[A/G]GCAAATAATTCAGTG	80176
rs748465505	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9326412	TCAGTGGGTGGTGTC[A/G]GAGGAGTCACCTCAC	80176
rs748487224	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9360506	CGCTCAGGAGGCCAG[A/G]TGTCTGCGATCAGGA	80176
rs748550085	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9317268	AGCACTGGAGAGGGA[A/G]GAGGAAGGGAAGAAG	80176
rs748668935	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9341833	TCAGCCTCCTGAGTA[G/T]CTGGAATTACAGGCA	80176
rs748689031	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9304276	GGTTCTGAGGCCTTC[A/T]GACTTGGCTGAGCCA	80176
rs748690311	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9346701	TGCCTCATTCCTCCT[C/G]ACCTCCTCCTCTTCC	80176
rs748702730	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9334785	GTACCTCATGTAAGT[G/T]CAATCATATAGTATT	80176
rs748708480	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9307084	AGGCACGTGCCACCA[C/T]GCCTGGCTAATTTTT	80176
rs748712979	in-del	-/TGAATAAGTGAACGAATGAATGAATAAG			intron-variant	SPSB1	GRCh38.p7	1:9298415	GAGTGAACGAATGAA[-/TGAATAAGTGAACGAATGAATGAATAAG]TGAATGAATAAGTGA	80176
rs748761558	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9335711	AGGCTGAGGCAGGAA[C/G]ATCACTTGAGCACTT	80176
rs748816392	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9304357	TCAGCCTCCATAACC[C/G]ATGAGCCAGTTCCCC	80176
rs748904294	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9313269	GCCAGACGTGGTGCC[A/G]GGCACCTATAATCCC	80176
rs748979653	in-del	-/GA			intron-variant	SPSB1	GRCh38.p7	1:9309283	AGAGAGAGAGAGTGT[-/GA]GAGAGAGAGAGAGAG	80176
rs749017985	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9343311	CTGCTTTCTGTTTCT[A/T]TGGATTTGCCTATCC	80176
rs749030713	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9321504	CTCCAGACCTTTACC[A/G]AACACTTACTGCGTG	80176
rs749044105	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9315276	GCGACAAAAGACCCC[A/G]TACTGGCTCCAAGGG	80176
rs749053694	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9354000	CTGAGATAAGGGGGT[C/T]GGGGCACCAAGTGTT	80176
rs749174615	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9307530	TCTGGCTAATTAAAT[C/T]TTGCATGGAAGATTG	80176
rs749179074	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9364322	CAGAAGACCTACTCC[C/T]GACAGCCAGGCCAGA	80176
rs749189929	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9339131	AGGCCTGGGGACCCT[A/C]CTGCGGGGGCTCCGG	80176
rs749318182	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9342053	GGCACTCAGGGACTG[A/C]GAAACAAAGCAAGGT	80176
rs749332071	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9325041	CTGCTGCCTCCTGAA[G/T]GGGCAGCCGGTGTGG	80176
rs749351966	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9357675	GACTGAGTCAACAGC[A/G]AACTCCACCTGTCCC	80176
rs749429213	snp	A/G	1.78886e-05	0.00299065	missense	SPSB1	GRCh38.p7	1:9356582	TACTTGAACGGACTC[A/G]ATCGTAAGTGTCTCC	80176
rs749463933	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9300640	GCCATGTGACCTGAG[C/T]TGCCCATCATGAAGT	80176
rs749521220	in-del	-/AC			intron-variant	SPSB1	GRCh38.p7	1:9296630	CATATATGCACACAT[-/AC]ACACACACGCTGGAT	80176
rs749538757	snp	A/C	3.332e-05	0.00408153	intron-variant	SPSB1	GRCh38.p7	1:9367423	ACCCAAGCTGCGCTG[A/C]CCTGCAGTTTCTCTG	80176
rs749636615	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9340321	TGTTTGGGGACTGGC[C/T]GGAGCCCCGCGGTCT	80176
rs749638452	snp	A/G	1.66319e-05	0.00288369	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9367598	CATCATACCGCCAGC[A/G]CGACAGCCACCTGGT	80176
rs749788207	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9327174	GGCCCTCTAAGCCCA[C/T]GGCCTCCACAGTGGC	80176
rs749819836	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9360597	CCCCTGGGGGCTGCC[A/G]GGAATCCTTGGCGTC	80176
rs749954372	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9337702	GGACTCCCTGGCCAC[C/T]GGGGCCCTGAGCCAA	80176
rs749970830	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9316404	TGTATTTATGTGTGT[A/G]CATATGTGCTTGTGT	80176
rs750030573	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9346216	GAGGGAGGGAACTTA[C/G]GTGATCTTCAGGTGA	80176
rs750032053	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9358012	CCTGCAGGCCAGGCA[A/G]GAGGCAGAGGGGGGT	80176
rs750079111	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9342968	AAGTTCTGTGCCTCT[C/G]TCTGCCCTGCACCCC	80176
rs750082863	in-del	-/T			intron-variant	SPSB1	GRCh38.p7	1:9324508	CGGCTCGGAGGGCTG[-/T]GGGCCCGGGACTCGG	80176
rs750104952	snp	C/T	0.000296863	0.0121796	synonymous-codon	SPSB1	GRCh38.p7	1:9356344	CAACCGGCTCTACCA[C/T]GATGGCAAGAACCAG	80176
rs750145200	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9301251	TCCCAGCACTTTGGG[A/G]GGCCAAGGTGGGAGG	80176
rs750163216	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9366780	GGTTTCACCATGTTG[A/G]CCAGGCTGGTCTTGA	80176
rs750186894	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9322895	CCGGACGCTCTTCTC[A/G]GCCCCTTTTTTTGTT	80176
rs750202420	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9338176	AGACATGGAGGTTGG[C/T]GGTTGGGGGGTGCCA	80176
rs750277007	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9332016	GTGTTGAAAATATGT[C/G]ACTCTTTTGTACGTG	80176
rs750335608	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9353617	ATGACCGTGCCCCTG[A/T]GATCAGAACCCTCTG	80176
rs750353064	snp	C/G	9.0981e-05	0.00674405	missense	SPSB1	GRCh38.p7	1:9367549	CCGCTGCCGGCTTCC[C/G]TCAAGGCCTACCTCC	80176
rs750355773	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9319444	CTCCTTCTCCTCCCT[A/C]TAGGATCTCAAAGTA	80176
rs750356944	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9341029	TTGTCTCTTCCTCCT[C/T]GGGCCCTGATTGCTG	80176
rs750412011	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9350691	CCCTGCAGGGCAGTA[C/T]GAGCCACGCCCTTTG	80176
rs750428575	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9297085	CCTTGTGCAATGCAG[A/G]CATGGGATTTGTGGC	80176
rs750438282	in-del	-/TCTT			intron-variant	SPSB1	GRCh38.p7	1:9306921	TTCTTTTACTTTTCT[-/TCTT]TTCTTCTTTTTTTTT	80176
rs750490957	in-del	-/ACGAGGTGGCTGATGCCTATAAATCCCAGC			intron-variant	SPSB1	GRCh38.p7	1:9332074	AAAAGCCTTGGCCAG[lengthTooLong]ACTTTGGGAGGCCAA	80176
rs750491357	in-del	-/AC			intron-variant	SPSB1	GRCh38.p7	1:9350104	GCCTCACATATCTAC[-/AC]ACACACACACACCCC	80176
rs750491674	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9304752	GTGGACGTGTCCAGA[A/T]GGCAACTGGGCTCAA	80176
rs750519309	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9347414	TTTGAAAAGGAATAC[A/G]TGCATTTTAAAAAAT	80176
rs750573690	snp	A/T			downstream-variant-500B	SPSB1	GRCh38.p7	1:9369857	TTTGTGGGGTTGTAG[A/T]ACTTGAGTTGACCGT	80176
rs750591947	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9343695	TAGGTTTTAGTCTCA[C/T]GGCAGATGCAGTTGT	80176
rs750602261	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9320279	ACAGACTGCAGGGCG[A/G]TCATCAGCCATTATT	80176
rs750661023	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9312888	AGAGGCAGTGCGTGC[C/T]GATTGTCCAAAGCCA	80176
rs750712051	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9354263	TTTGTCTCCTTTACT[C/T]GGGCACCCTAGTAAC	80176
rs750720392	in-del	-/C			intron-variant	SPSB1	GRCh38.p7	1:9306916	TTTTTTCTTTTACTT[-/C]TTCTTCTTTTCTTCT	80176
rs750727274	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9342823	TGGAGAACAGAAAGG[C/G]GAGGGGGCAGAGGCC	80176
rs750733634	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9321135	AAAAGAAAACAACAA[A/C]CAAAAAATCCCCCCA	80176
rs750804833	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9316387	AGGGGCATGTGTGCA[C/T]GTGTATTTATGTGTG	80176
rs750821393	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9353315	CCACACCAGACCCAG[C/G]TCTCTCCCCCTTCCC	80176
rs750827389	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9296160	AAGCATAATAATAGC[A/G]GGAAATGGTTTCATG	80176
rs750864923	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9329138	TCCCAAGGGGGAGAA[C/T]TGAAGACACCTAAGG	80176
rs750877507	snp	C/T	1.66776e-05	0.00288765	synonymous-codon	SPSB1	GRCh38.p7	1:9356521	GGGCAAAAAACTGTA[C/T]CCTGTAGTGAGTGCC	80176
rs750883425	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9307223	ATGAGCCACTGTGCC[C/T]GGCCGTCTTTTCTCA	80176
rs750893858	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9363851	GACTACAGGCATGCA[C/T]GACCACACCCAGCTA	80176
rs750912930	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9329792	GCATCGGACACATGG[C/T]GGTGGGGCCGTGGGG	80176
rs750918927	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9295605	CCCTTGGAATCATCA[C/T]AGATGTTGAATTTCT	80176
rs751023957	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9362813	TTCCTCAGGCTTCTG[C/T]TCCCAGAAATAGCGC	80176
rs751036487	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9354019	GCACCAAGTGTTCCC[A/G]CATGGGAAGGTTCTG	80176
rs751044624	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9296745	GTTGACTGTTACTCT[A/G]TGCGGGGCAAGAGTC	80176
rs751143857	in-del	-/CTTGATGTTGTAG			intron-variant	SPSB1	GRCh38.p7	1:9297630	AGCGGAGATTCTGCA[-/CTTGATGTTGTAG]CTTGATGTTGTAGCT	80176
rs751160831	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9338210	AGCTCTCCCCTACCC[C/T]GTTTCTTCAGGCTTC	80176
rs751305241	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9311463	TACCCACACCACCCA[C/G]CACCAACAAATATTC	80176
rs751392382	in-del	-/CTTTT			intron-variant	SPSB1	GRCh38.p7	1:9306922	TCTTTTACTTTTCTT[-/CTTTT]CTTCTTTTTTTTTTT	80176
rs751446868	snp	C/T	1.66324e-05	0.00288374	intron-variant	SPSB1	GRCh38.p7	1:9367411	TGCTGAACACCCACC[C/T]AAGCTGCGCTGACCT	80176
rs751502055	snp	A/G	1.662e-05	0.00288266	missense	SPSB1	GRCh38.p7	1:9367481	TGGATTTGTGCCGTC[A/G]CTCGGTGCGCCTGGC	80176
rs751508951	in-del	-/GATG			intron-variant	SPSB1	GRCh38.p7	1:9357271	ATGAGTGGGTAGATG[-/GATG]GATGGATGGATGGAT	80176
rs751602212	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9366935	TGGTAACAGAAAATG[A/C]TTCCCTTCCTGAAGC	80176
rs751607761	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9349739	GGGCCAGTTGTGTGA[A/G]GAAGGTCCTTTCGGG	80176
rs751620227	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9326976	GACTTCCAGATTGGA[A/G]AGGCACCTGGATCCC	80176
rs751641417	snp	A/T			upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291928	TGATTTTCAGCACCG[A/T]AAAATGAGAGACATC	80176
rs751759865	snp	A/G	4.66266e-05	0.00482816	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9367577	TCCTCTACCAGTGAC[A/G]TTCGCCATCATACCG	80176
rs751810595	snp	C/G			utr-variant-3-prime	SPSB1	GRCh38.p7	1:9368340	GGGCACATGTGCACA[C/G]GTGCCCAGGCACAAG	80176
rs751811045	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9347525	TTCTCTGTACCTACA[A/G]ACATAAATAGGCGCA	80176
rs751821229	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9304798	CCCACCTCAGCCCCC[C/G]AGTAGCTGGGACTAT	80176
rs751824572	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9359794	GGCCAGGCCAGGGAC[A/G]AGCCAGGCTTGTCCC	80176
rs751833381	snp	G/T	1.81246e-05	0.00301031	utr-variant-5-prime	SPSB1	GRCh38.p7	1:9355844	CGAGACCACGAGATT[G/T]ATGAGTTTGCCTTGG	80176
rs751892841	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9313037	CCACACATTAACTTA[C/T]TGACTGCTGCACAGA	80176
rs751952219	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9302381	ATTGTGTAGAATGAT[C/T]GGGCTGCCCCAGATG	80176
rs751981794	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9341635	GTTTCCTCTTGGGAG[A/G]GATGTTTTCTAGCAG	80176
rs751984624	snp	C/T	1.65184e-05	0.00287384	missense	SPSB1	GRCh38.p7	1:9356327	GGCTGGGACTTGGGG[C/T]GCAACCGGCTCTACC	80176
rs752023338	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9298152	TGGATAGTTAATCAT[A/G]GTGTTCCTAGAAGTG	80176
rs752023898	snp	A/C	1.75585e-05	0.00296293	synonymous-codon	SPSB1	GRCh38.p7	1:9356221	CATGAGACAGCGGGG[A/C]ACACACGCCGTGGTG	80176
rs752030541	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9331065	ATGCCATTATTTTAT[C/T]AGAATGGGCTCTCCT	80176
rs752072878	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9358561	GGGCATATCCTGCCT[A/G]GGACCTAGAATCTTG	80176
rs752118225	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9330421	AGTGAGCCAAGATTG[C/T]GTCACTGCGCTCCAG	80176
rs752164359	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9366635	CTAGAGTGCAGTGGC[A/G]TGATCTCAGCCCACT	80176
rs752176183	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9353478	GAGATCATGGATGTG[A/C]GGTCACAGTATTCAC	80176
rs752202998	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9357838	AGAACGGCTCACCCC[A/G]TGTACGGCCCTCTCT	80176
rs752211631	snp	C/T	1.66286e-05	0.0028834	intron-variant	SPSB1	GRCh38.p7	1:9367399	GTTAGCGCTGTTTGC[C/T]GAACACCCACCCAAG	80176
rs752266454	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9330522	GTCTCCTTACTCCTA[C/G]CACCCCAAGGGAACC	80176
rs752279631	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9331155	ATGTGGTTCTACCTC[A/G]TCTTTTTAATTGCTG	80176
rs752292653	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9308968	ACATGAGCTCCCTGC[C/G]AGGGGCTGGGCGGGC	80176
rs752359028	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9364903	TCACCCCAGGCTGGA[A/G]TGCGATGGTGTGATC	80176
rs752630317	in-del	-/TGTC			intron-variant	SPSB1	GRCh38.p7	1:9293995	GTGTGTGAGTCTGTG[-/TGTC]TGTCAATGTGTGCCT	80176
rs752688288	snp	A/G	8.59542e-05	0.00655513	missense	SPSB1	GRCh38.p7	1:9356559	GCCACTGTGAGATCC[A/G]AATGCGCTACTTGAA	80176
rs752738682	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9319565	TGGAGGAGGTGGGGA[A/G]CGCTTGGGTCAGGCC	80176
rs752742495	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9358225	CTTTGGAAGCCTCCC[C/T]GCCCCTCTTTCTCTT	80176
rs752783477	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9333629	AGCCACCATGCCCGC[C/T]CTCCTTGTCAGCTTC	80176
rs752845945	in-del	-/GGGGGC			intron-variant	SPSB1	GRCh38.p7	1:9360212	AGAGGCCAGGAGGGT[-/GGGGGC]TGAAGGGACCCAGTA	80176
rs752885896	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9325063	CCGGTGTGGATGCAG[C/T]GGCTGCACTCGCTGG	80176
rs752959694	in-del	-/GG			intron-variant	SPSB1	GRCh38.p7	1:9295232	GTGTGTGTGTGTGTG[-/GG]TGTGTGTGTGCGCGC	80176
rs752975296	snp	C/T	1.96473e-05	0.00313421	missense	SPSB1	GRCh38.p7	1:9367562	CCCTCAAGGCCTACC[C/T]CCTCTACCAGTGACG	80176
rs753016540	in-del	-/TTTCTTC			intron-variant	SPSB1	GRCh38.p7	1:9306924	TTTTACTTTTCTTCT[-/TTTCTTC]TTTTTTTTTTTTTTT	80176
rs753016568	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9326429	AGGAGTCACCTCACA[C/T]TGCCTGGGCACAGTG	80176
rs753020809	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9346569	ATTGATCTGAAAGCA[C/T]TTTGGGGGAAGGTGG	80176
rs753105691	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9315379	CTTTGTGGCTGCCTT[C/T]TGGGTACCAGGCACA	80176
rs753109165	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9345887	GGTCCCTCCTCAAGT[A/T]GGCAGTTGGCAGGGT	80176
rs753181342	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9361806	GAGTGGGGAGACACA[G/T]GGCCTGGCCTGACCC	80176
rs753185303	snp	A/G	5.16054e-05	0.00507937	synonymous-codon	SPSB1	GRCh38.p7	1:9356128	CTTTCACCGGCATCC[A/G]GTGGCCCAGAGCACG	80176
rs753194516	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9305201	CTCTTCATGCTGCCT[C/G]GTCCCGCCTCGGCTG	80176
rs753201922	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9314026	ACTAAAAATACAAAA[A/G]TTAGCCAGGTGTGGC	80176
rs753221058	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9323416	GCCTCCCTCGCGGCC[C/T]GTTGGCAGAGATCTC	80176
rs753238760	in-del	-/A			intron-variant	SPSB1	GRCh38.p7	1:9294696	CCATCCCTGGTGACT[-/A]AAGGTTTGATGTCCT	80176
rs753246106	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9302455	TCAACTGGGTGGGGA[C/G]GATCTGCCCTCCATG	80176
rs753355319	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9341556	AGCTGAACATTGCCA[A/G]ACCATCTCTCTGGTT	80176
rs753403238	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9322122	TAACGACCCACATTC[C/T]CAGGACTTAGCTCCT	80176
rs753411342	snp	A/C	1.68752e-05	0.00290471	synonymous-codon	SPSB1	GRCh38.p7	1:9356539	TGTAGTGAGTGCCGT[A/C]TGGGGCCACTGTGAG	80176
rs753420861	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9366673	CCATCTCCCAGGTTC[A/G]AGCGATTCTCCTGCC	80176
rs753460965	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9301081	GCACCTTGCTTCGAA[C/G]GAGAGATGGCCAGAT	80176
rs753465487	snp	A/C	1.64819e-05	0.00287066	missense	SPSB1	GRCh38.p7	1:9356365	CAAGAACCAGCCAAG[A/C]AAAACATACCCAGCC	80176
rs753604433	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9340865	GCGAGCACATGAAAC[A/G]CACATTTGTAGTCCT	80176
rs753772192	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9326899	CAAGGGAGCAGCTGG[C/T]GCCTTTTTTAGGTGG	80176
rs753811527	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9317639	CACGCCCAGATATAT[A/G]TATATTTTTGTATTT	80176
rs753817971	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9302444	AATTGAGTCACTCAA[C/T]TGGGTGGGGAGGATC	80176
rs753823244	in-del	-/T			upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291915	GCTAAACCAAACTGA[-/T]TTTTCAGCACCGTAA	80176
rs753866448	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9310350	TCTCATGTGAGGTTC[C/T]TGGGGCGCCTTCCTG	80176
rs753919091	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9342709	GGCACACATCCGAGA[C/T]GCAGGCACACATCCC	80176
rs754008543	snp	C/T	1.69752e-05	0.0029133	synonymous-codon	SPSB1	GRCh38.p7	1:9356110	GGAGGACGACAAGCT[C/T]ATCTTTCACCGGCAT	80176
rs754009234	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9295992	ATCAGTGAAATCCAG[A/C]CTCTAAGGGACTTCG	80176
rs754052035	in-del	-/TG			intron-variant	SPSB1	GRCh38.p7	1:9348942	TCGTGCAAGAATGTG[-/TG]TGTGTGTGTGTGTGT	80176
rs754080344	in-del	-/GTGTG			intron-variant	SPSB1	GRCh38.p7	1:9295238	TGTGTGTGTGTGTGT[-/GTGTG]CGCGCGTGCGGTTGG	80176
rs754101419	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9318076	GCAGGTTGGGGAAAC[A/G]CAGCGATTGTTCTGG	80176
rs754157675	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9351965	CCCTTTACCTGCCTG[C/T]CCTGCCCGGGGAAAA	80176
rs754201580	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9328823	GGGCAGGGGAATTGT[C/T]GATGTGAGGCTTGTG	80176
rs754208907	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9362684	TGGGTTGAAATCTCT[C/T]GGGGAACAGTGAGAC	80176
rs754239182	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9306708	GAGGAAGAAATGAGC[A/G]ATCCGAGAGATAGGT	80176
rs754265437	in-del	-/AAAACAAC			intron-variant	SPSB1	GRCh38.p7	1:9321125	CCCTCCCCCGAAAAG[-/AAAACAAC]AACCAAAAAATCCCC	80176
rs754289601	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9328171	AGCCAGACGAACGTG[A/G]CTGTGTGGAGGATTC	80176
rs754322657	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9323100	CCCAGCTCCGGCCTT[C/T]GAGGACTTTGCGGCC	80176
rs754329039	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9306023	GGTTCGTGCTTTAGG[A/G]AACGAAGGCGTGTTG	80176
rs754370763	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9346000	CGGAGCATGCCCCGA[A/G]CCCTTCCACCACCAA	80176
rs754416109	snp	C/T	1.6477e-05	0.00287024	missense	SPSB1	GRCh38.p7	1:9356385	CATACCCAGCCTTTC[C/T]GGAACCAGATGAGAC	80176
rs754439299	snp	A/G	1.66175e-05	0.00288244	missense	SPSB1	GRCh38.p7	1:9367465	GAGCCGCTGCCGCTC[A/G]TGGATTTGTGCCGTC	80176
rs754456118	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9364887	ACAGAGTCTTGCTCC[A/G]TCACCCCAGGCTGGA	80176
rs754482500	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9336988	GCCTGACTCCCTATC[A/G]TGGCATTCAAGGCCC	80176
rs754518680	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9353484	ATGGATGTGAGGTCA[C/T]AGTATTCACAGAACT	80176
rs754526154	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9338949	TGGAAAACCCGGCCG[A/C]TTACCTTGTAATTGT	80176
rs754541677	snp	A/G	3.41804e-05	0.00413389	synonymous-codon	SPSB1	GRCh38.p7	1:9356554	CTGGGGCCACTGTGA[A/G]ATCCGAATGCGCTAC	80176
rs754604017	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9354083	CGGGAACAGGGTCTC[C/G]TGGGGCCTCTTCCCA	80176
rs754620110	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9311466	CCACACCACCCAGCA[A/C]CAACAAATATTCGCT	80176
rs754671375	in-del	-/TTCTTC			intron-variant	SPSB1	GRCh38.p7	1:9306925	TTTACTTTTCTTCTT[-/TTCTTC]TTTTTTTTTTTTTTT	80176
rs754722099	in-del	-/T			upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291176	CTGGTCCTGAACTTC[-/T]TTTTTTTTTTTTTTT	80176
rs754807083	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9366155	GCTGCAGCTGGAAGC[A/G]CTCTGTAACCCTGGG	80176
rs754864174	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9358195	TTAGGCATGCGCAAA[C/T]GCTTACACATTTCTC	80176
rs754894208	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9333040	CTGAGCTTCTGCCCT[C/T]GTGGGCTGCGTCAGG	80176
rs754971575	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9364862	CGTTGTTGTTGTTGG[C/T]TTTTCTGAGACAGAG	80176
rs754991670	snp	A/G			utr-variant-3-prime	SPSB1	GRCh38.p7	1:9368204	TTTAACAATAACAAA[A/G]GCCATTTATTTATTC	80176
rs755047859	snp	A/T	1.70359e-05	0.0029185	missense	SPSB1	GRCh38.p7	1:9356116	CGACAAGCTCATCTT[A/T]CACCGGCATCCGGTG	80176
rs755125682	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9317763	GTTGGGATTACAGGC[A/G]TGAGTCACCGTGCCT	80176
rs755147533	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9349764	TTCGGGAGTTCCCAA[A/C]CCACCGTTTTATGGC	80176
rs755161745	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9327032	GGGGTCTTGGCTTAG[C/G]GGCAGGTGCTCAGGG	80176
rs755177136	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9326310	TGATCCTCAGTCTCC[C/G]TGCGCACTGGAGGTG	80176
rs755226312	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9304894	CCCAGGCTGGTCTCG[A/T]ACTCCTGGGTTCAAG	80176
rs755253853	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9330328	CAAAATACAAAATTA[A/G]TCGGGCGTGGTGGTG	80176
rs755265031	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9335412	GAGGCTTAGACAGGA[A/G]AATCACTTGAACCCA	80176
rs755285235	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9302382	TTGTGTAGAATGATC[A/G]GGCTGCCCCAGATGT	80176
rs755384722	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9303958	GTTTGGCATTTGTGT[A/G]GAATGATTGGGCTGC	80176
rs755402246	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9358677	GACAGACAGATGAGG[A/G]GACTGCCAGACCTGC	80176
rs755409794	in-del	-/GT			intron-variant	SPSB1	GRCh38.p7	1:9294226	TGTGTGTGTCTTTGC[-/GT]GTGTGTGTCTTTGTG	80176
rs755420089	snp	A/G	4.94849e-05	0.00497393	missense	SPSB1	GRCh38.p7	1:9356034	TGCCCCCTGTGTCCT[A/G]TGATGTCCAGCTGCT	80176
rs755446610	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9301377	TGGTAGCTCATGCCT[A/G]CAGTCCCAGCTACTT	80176
rs755457385	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9340328	GGACTGGCCGGAGCC[C/T]CGCGGTCTGACTTTC	80176
rs755473255	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9313113	AGTTTAAAAAAAGTC[A/C]AGTCCGGGCGCGGTG	80176
rs755487543	in-del	-/TGGATGGG			intron-variant	SPSB1	GRCh38.p7	1:9357142	GGATGAGTGGATGGA[-/TGGATGGG]TGGATGGATGGGTGG	80176
rs755527632	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9321326	TACAGAGAAAGCCCG[C/T]GTGTGTGGTGGAGCT	80176
rs755551062	in-del	-/TTT			intron-variant	SPSB1	GRCh38.p7	1:9333329	CTTCTTGTCAGCTTC[-/TTT]TTTTTTTTTTTTTTT	80176
rs755577494	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9343095	ATTGAGGTGAAATTC[A/G]CATAACATTCACCTT	80176
rs755616113	in-del	-/TTGG			intron-variant	SPSB1	GRCh38.p7	1:9356847	TAGATGGATGAATGA[-/TTGG]TTGGATGGATGGATG	80176
rs755643069	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9340017	TGAACCACCTGGGCA[C/T]GCAGGTCACCCAGAG	80176
rs755715206	snp	A/G	1.7393e-05	0.00294893	synonymous-codon	SPSB1	GRCh38.p7	1:9356236	CACACACGCCGTGGT[A/G]GGGGTGGCGACGGCA	80176
rs755735112	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9338563	GAAGTATACTTTCTT[A/C]TTTGCTGGTGAGTTT	80176
rs755768724	snp	A/G	6.59696e-05	0.00574286	missense	SPSB1	GRCh38.p7	1:9356345	AACCGGCTCTACCAC[A/G]ATGGCAAGAACCAGC	80176
rs755789438	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9364910	AGGCTGGAGTGCGAT[A/G]GTGTGATCTCGGGTC	80176
rs755842143	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9364254	CAGGCCAGATGCAGG[C/T]GCGCTCCCAAGCAGA	80176
rs755893839	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9297412	CCAGTTGTGAACACA[C/T]CTTGCCAGACAGTCA	80176
rs755893875	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9308078	AAATCCTGTTAACCC[A/G]TCTGGGACCAGAACT	80176
rs755907132	snp	A/G	3.32436e-05	0.00407685	missense	SPSB1	GRCh38.p7	1:9367490	GCCGTCGCTCGGTGC[A/G]CCTGGCCCTGGGGAG	80176
rs755953992	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9317626	AGGTATGCACTACCA[C/T]GCCCAGATATATATA	80176
rs756041923	in-del	-/G			intron-variant	SPSB1	GRCh38.p7	1:9366605	TTTGGACCGAGTCTT[-/G]GCTCTGTCGCCCAGC	80176
rs756056958	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9325460	CAGAGAGATGGATGC[C/T]TGCCCACCTCTTCAG	80176
rs756153934	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9342054	GCACTCAGGGACTGA[A/G]AAACAAAGCAAGGTC	80176
rs756154231	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9359144	AGGATGCTTTTTCCT[C/T]TCCACCAGCATCAGA	80176
rs756174110	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9360323	CGGCTGAGAACCGTC[C/T]ATCAGCTTTGGCAAC	80176
rs756183566	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9332362	AATGTTTGGCGCTAA[C/T]GTGGGAAGCCAAGAA	80176
rs756189989	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9341896	TAGTAGAGATGGGGT[G/T]TCTCCATGTTGGTCA	80176
rs756201548	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9366955	CTTCCTGAAGCTAGT[G/T]CTGGGGGTGCGTGCC	80176
rs756237714	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9351756	AAAGGAAGTTGGGAA[A/G]GCACTGTCATCTTTA	80176
rs756253386	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9309387	CAGTGGTGCGGTCAC[A/G]GCTCACTGCAGCCTC	80176
rs756300548	in-del	-/TT			intron-variant	SPSB1	GRCh38.p7	1:9347944	CAGTTTCCCTGCAAC[-/TT]TTTTTTTTTTTTTTT	80176
rs756316343	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9319566	GGAGGAGGTGGGGAG[C/T]GCTTGGGTCAGGCCC	80176
rs756337203	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9318814	TCACTGCATATAGTG[A/G]GGGACAGTCACATGA	80176
rs756361255	in-del	-/AG			intron-variant	SPSB1	GRCh38.p7	1:9295234	GTGTGTGTGTGTGTG[-/AG]TGTGTGTGCGCGCGT	80176
rs756380273	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9361822	GGCCTGGCCTGACCC[C/T]GGGCCTGCCCGCCAC	80176
rs756411903	in-del	-/T			utr-variant-3-prime	SPSB1	GRCh38.p7	1:9369205	TTATTATTTTGACGG[-/T]TTTTTTTTTTCGGGG	80176
rs756435315	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9305998	GCAATTGCGAGTAAC[A/G]TGGGAGAGGGGTTCG	80176
rs756504317	snp	A/G			upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291085	CTCCCGAGTAGCTGG[A/G]ATCGCAGGCACGTAC	80176
rs756560706	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9315418	TGTGTCGTTGTCTCA[C/T]GCAAGTCTTTACAAT	80176
rs756571750	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9360555	CCTCCGAGCTCTGAG[C/G]GGGAGCCCGCCCCAT	80176
rs756592263	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9305207	ATGCTGCCTGGTCCC[G/T]CCTCGGCTGGCCCGT	80176
rs756602227	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9310522	ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA	80176
rs756674581	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9344876	CTGGAGGGACATGAG[C/G]GTGACCCAAGGACCA	80176
rs756692396	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9336911	GAAGGAGCCTTCTAA[C/T]CTGGCACCTCCCCTT	80176
rs756716344	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9335637	GAGATCCCATCTCTA[A/C]AAAAACTAAAAAACT	80176
rs756729667	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9346073	AGAACCCCAGTGAGC[A/G]GGCAGAGCCCAGGCA	80176
rs756734034	snp	C/T			utr-variant-3-prime	SPSB1	GRCh38.p7	1:9369431	TTCTTTCCTACCAGC[C/T]CAGAGCCTTGTGGCT	80176
rs756809345	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9356980	TGGATGGATGTGGGT[A/G]GATGGGTGGGTAGGG	80176
rs756965476	in-del	-/GAGTGT			intron-variant	SPSB1	GRCh38.p7	1:9309300	AGAGAGAGAGAGAGA[-/GAGTGT]GTGTGTGTGTGTGTG	80176
rs756989896	snp	C/G	5.24682e-05	0.00512165	missense	SPSB1	GRCh38.p7	1:9356148	CCCAGAGCACGGACG[C/G]TATCAGGGGCAAAGT	80176
rs757004645	in-del	-/GTGA			intron-variant	SPSB1	GRCh38.p7	1:9293932	CATGTGGGTGTGTGT[-/GTGA]GTGTGTCTCTAAGTG	80176
rs757023185	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9331920	CTTTTTCTTTGCATT[G/T]TCTGTTCCAGTCCTC	80176
rs757078391	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9309084	GAGATTGACTGCCAT[G/T]AGGAGGACCGGGAGA	80176
rs757093127	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9308203	GAGAGGATGACAGAA[G/T]TGTGCTTAGGAGCTT	80176
rs757126416	snp	C/T	1.66189e-05	0.00288256	synonymous-codon	SPSB1	GRCh38.p7	1:9367482	GGATTTGTGCCGTCG[C/T]TCGGTGCGCCTGGCC	80176
rs757138340	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9318553	TCCAACCTGGATCCT[A/G]GACAAGTTACTCAGC	80176
rs757169815	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9318213	GGAGGCCCATGATGC[C/T]CCCAGATCCTCCACC	80176
rs757231336	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9331972	ATAAAAGGACCAAAA[A/G]CAAATGTGCCAAACT	80176
rs757292587	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9339135	CTGGGGACCCTACTG[C/T]GGGGGCTCCGGAGGT	80176
rs757326207	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9334442	ACCAGGCTGGTCTCG[A/T]ACTTCTGGCCTCAAG	80176
rs757350704	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9324305	ATGGCATCGATGAAT[C/T]GTGTCCCGATTAGCT	80176
rs757366704	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9345552	GCTTCTCGTCTGCAT[C/G]AGGCACAGTCCGTTG	80176
rs757411749	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9333238	AGCCTGTCCCTAATT[C/G]TTAGCCATTTAGGGC	80176
rs757481807	in-del	-/CTGA			intron-variant	SPSB1	GRCh38.p7	1:9298381	CCCATGAATGAATGA[-/CTGA]ATGAGTGAATGAATG	80176
rs757492316	snp	A/T	1.8124e-05	0.00301026	utr-variant-5-prime	SPSB1	GRCh38.p7	1:9355845	GAGACCACGAGATTG[A/T]TGAGTTTGCCTTGGG	80176
rs757504198	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9311886	CTCTGCCAGATGAAA[G/T]AGCTATGCTCAGACA	80176
rs757527750	snp	C/T	1.74995e-05	0.00295795	synonymous-codon	SPSB1	GRCh38.p7	1:9356227	ACAGCGGGGCACACA[C/T]GCCGTGGTGGGGGTG	80176
rs757550158	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9351982	CTGCCCGGGGAAAAC[A/G]CCCCACCCTCTTTCC	80176
rs757567851	in-del	-/A			intron-variant	SPSB1	GRCh38.p7	1:9347646	GTTACATTTTCTGTT[-/A]ACGTCACCACTTTGG	80176
rs757596777	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9320292	CGGTCATCAGCCATT[A/G]TTGCCTCTTGGGCCG	80176
rs757605342	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9362695	CTCTCGGGGAACAGT[C/G]AGACAGTTGTGGGTT	80176
rs757700158	in-del	-/GTG			intron-variant	SPSB1	GRCh38.p7	1:9295234	TGTGTGTGTGTGTGT[-/GTG]TGTGTGCGCGCGTGC	80176
rs757702276	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9298000	AAAACTTAAATGCAA[C/T]GGGAGTAATTGCATT	80176
rs757806206	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9361924	CTTGTGGGTCCTCTG[A/G]CTCTACCCCCACTGC	80176
rs757842840	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9328276	CGGAGGTCCTCCAAA[C/T]TGTCATCCCTCATGA	80176
rs757868375	snp	A/G	1.66283e-05	0.00288338	intron-variant	SPSB1	GRCh38.p7	1:9367402	AGCGCTGTTTGCTGA[A/G]CACCCACCCAAGCTG	80176
rs757919948	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9310458	AGCACTTTGGGAGGC[C/T]GAGGCAGGCAGATCA	80176
rs757939673	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9334837	TTTTACTTCATATAA[C/T]GTGTTCAAGATTCAC	80176
rs757946123	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9353779	AAAAATTAGCTGGGC[A/G]TGGTGGTGGGCGCCT	80176
rs757992621	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9295541	GCTGCTGTAGTAAGG[C/T]TGGATCCACCCTTCA	80176
rs757992825	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9337723	CCTGAGCCAATATCC[A/G]TGGAGGCTGCAGAGC	80176
rs758057455	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9319333	GCTGCCCTGGCCGTG[C/G]CATGTTGCTCACCAA	80176
rs758080768	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9346291	TCATTCTTTCCCCAT[C/T]TTGGGGCAAAACAAT	80176
rs758119075	snp	C/G/T			intron-variant	SPSB1	GRCh38.p7	1:9315763	CACCTACGGAGGGAC[C/G/T]GCACTGCTCACAAGG	80176
rs758171407	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9323831	TTCTGCTGTTGCCCA[C/T]GGACGGCAGGGGCTG	80176
rs758194999	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9357092	ATGGATGGGTGGGTG[A/G]ATGGATGGATGGATG	80176
rs758220862	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9300438	GGTGGTTGAGGTCAG[C/T]GGCAGACAGGGAGGC	80176
rs758255203	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9322920	TTTGTTGTCTGGCTG[A/C]GTCAGACGTCTGGGC	80176
rs758285331	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9310427	GCCGGGCACAGTAGC[C/T]CATGCCTGTAATCCC	80176
rs758363286	in-del	-/AGAGTG			intron-variant	SPSB1	GRCh38.p7	1:9309299	GAGAGAGAGAGAGAG[-/AGAGTG]TGTGTGTGTGTGTGT	80176
rs758373348	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9309155	GGCCCAGGGGTCGTC[A/G]GTGGGCATGGGGTGT	80176
rs758393018	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9360301	AGCAGCAGGTCAAGT[A/G]CATGGACGGCTGAGA	80176
rs758416965	in-del	-/TGGA			intron-variant	SPSB1	GRCh38.p7	1:9357094	GGATGGGTGGGTGGA[-/TGGA]TGGATGGATGGATGA	80176
rs758433503	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9331588	CCACTGCCTTAGCCT[C/T]CCAAACTGCTGGGAT	80176
rs758452383	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9330046	ACCATCTGCATGGGT[C/T]TCTTACCTCCATTCT	80176
rs758459549	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9326251	CCCTTTCCAATCTGC[A/G]TTTATTCCCAGCACC	80176
rs758483422	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9348733	CTTAAATGGCTGTTC[A/G]AAGCTGGCCGAGGGA	80176
rs758544871	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9359217	CGTGGTCAGTTGACT[G/T]TAGAGGTTCCAGATT	80176
rs758549515	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9325558	TGAGCAGGTGGCACC[A/G]TGGAACAGACAGTCA	80176
rs758574590	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9334517	TGAGCCACCGTGCCT[A/G]GCCAAATTTACCATT	80176
rs758612603	in-del	-/TTCTTTTCTT			intron-variant	SPSB1	GRCh38.p7	1:9306920	TTTCTTTTACTTTTC[-/TTCTTTTCTT]CTTTTTTTTTTTTTT	80176
rs758638826	snp	A/G	2.20146e-05	0.00331765	synonymous-codon	SPSB1	GRCh38.p7	1:9367572	CTACCTCCTCTACCA[A/G]TGACGTTCGCCATCA	80176
rs758640258	snp	A/G			downstream-variant-500B	SPSB1	GRCh38.p7	1:9369939	GCTCTAGGGGAAGGA[A/G]CAGGTCCTTCATTCG	80176
rs758646851	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9303727	TAGGTGGAACTATGA[C/T]CTTGATACTGTCCTT	80176
rs758660428	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9342909	ATGGTGTCCTTTTGT[A/G]TAACCCTGGCTAATA	80176
rs758671936	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9343814	TTTTTGAGACAGAGT[C/T]TCGCTCTGTTGCCTA	80176
rs758676493	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9321176	CTGGAAAAAGCTCTT[A/C]AACCTTCTTAGTTTA	80176
rs758734781	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9312906	TTGTCCAAAGCCAGG[C/T]CCAAGAACATGTGTC	80176
rs758751841	in-del	-/CT			intron-variant	SPSB1	GRCh38.p7	1:9337796	TCTCTTGCTCCCTCA[-/CT]CTGTCTCTGTCTCTC	80176
rs758759350	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9302606	TTGGACTCTGGGACT[C/T]GTACGAGTGGTCTCC	80176
rs758842481	snp	A/G	3.51747e-05	0.00419358	synonymous-codon	SPSB1	GRCh38.p7	1:9356215	GTGGGCCATGAGACA[A/G]CGGGGCACACACGCC	80176
rs758847220	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9312169	TATTTTAATTTTTTA[A/G]TTTTTTAATTTTTTT	80176
rs758899224	snp	C/G/T			intron-variant	SPSB1	GRCh38.p7	1:9320466	GATTGGGAGGCCTCT[C/G/T]GAGGGCTGGGAGAAG	80176
rs758932454	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9314317	CCTTCCTCCCTCCCG[C/G]TCCTAAATATACAAG	80176
rs759003726	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9352028	CCAGGCCCTCCCTCC[A/C]ACAGACTCCCATCCC	80176
rs759012301	in-del	-/GTG			intron-variant	SPSB1	GRCh38.p7	1:9295232	AGTGTGTGTGTGTGT[-/GTG]TGTGTGTGCGCGCGT	80176
rs759017722	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9357567	GCTTAGAGTCTTTCT[C/T]TTCTGCCAGAGGCTT	80176
rs759099730	snp	C/T	1.66081e-05	0.00288163	synonymous-codon	SPSB1	GRCh38.p7	1:9356080	CAACGACCGATCGCT[C/T]AATGTCTTTGTGAAG	80176
rs759126116	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9318230	CCAGATCCTCCACCA[C/T]GAATGCAGCCGGCAG	80176
rs759126137	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9308002	GGTGCTCCTCCTCCT[C/G]GGGGGCAGGAGCTGT	80176
rs759267903	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9304511	GGCCAGGGAGATGGC[A/G]GTTCATATCCCTGAC	80176
rs759279396	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9313340	GGGAGGCAGAGGCTG[C/T]AGTGAGCCAAGATTG	80176
rs759394920	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9359106	CTCAGAGCATCACAG[A/C]CGGGCGCTATTAGTC	80176
rs759400809	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9343598	AGGGAATTCATAAGC[C/T]CATCACTCTAAACAC	80176
rs759448220	snp	A/G			downstream-variant-500B	SPSB1	GRCh38.p7	1:9369535	TTAAAATATCAAACC[A/G]TTTTTGAATTCCTCG	80176
rs759448677	snp	A/G	1.68105e-05	0.00289914	missense	SPSB1	GRCh38.p7	1:9355949	AGGGACCCCACGTAC[A/G]GGCCCCTGAAGCAGG	80176
rs759488234	snp	C/T			upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291346	TGCCCGCCACCACGC[C/T]TGGCTAATTTTTTAT	80176
rs759490568	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9342700	GGGGTCTGGGGCACA[C/G]ATCCGAGATGCAGGC	80176
rs759520829	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9327965	GCCTCAGTTTCTCAC[C/T]AAAGTGCAAGCCGCT	80176
rs759538645	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9359202	ATGGGCCCTGGGCCA[C/T]GTGGTCAGTTGACTT	80176
rs759561853	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9306669	AGTCTTACTCTTCAG[C/T]ACCATTTGCCACAAA	80176
rs759587749	in-del	-/G	1.65236e-05	0.00287429	frameshift-variant	SPSB1	GRCh38.p7	1:9356323	CTGGGGCTGGGACTT[-/G]GGGCGCAACCGGCTC	80176
rs759601207	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9362401	TTTGGCTGTGCTCTT[A/T]CGTAAGAACTGCGTA	80176
rs759622237	in-del	-/GTGTGTGCAT			intron-variant	SPSB1	GRCh38.p7	1:9350574	GCACACAGTGTACAC[-/GTGTGTGCAT]GTGTGTGCATGTAGG	80176
rs759628268	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9294791	AGAACAGCAAGCAAG[G/T]AAGGGGATGGGGGCC	80176
rs759675202	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9337896	GAGCACCTTTAGGGG[C/T]GGGAGGGGTAACTTA	80176
rs759769702	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9318922	GGGCCGGGCGCAGTG[G/T]CTCACACCTGTAATC	80176
rs759785340	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9305899	TGGCAGGGGTGGCCA[A/G]GTTGGAAAGGCGGGA	80176
rs759823990	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9323173	GAGGGGGGTATCCAT[A/G]GGGCCTCTGTCCCGG	80176
rs759870242	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9343162	CAATATAGTATACTA[C/T]CACCTCTGTCTTGTT	80176
rs759870520	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9355582	GCCAGGGAACGGGGG[A/T]TTTCATTCTGCGCCA	80176
rs759934939	snp	C/T	6.65059e-05	0.00576616	missense	SPSB1	GRCh38.p7	1:9367460	CAGCCGAGCCGCTGC[C/T]GCTCATGGATTTGTG	80176
rs759945527	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9344439	TCTCGTGACGGGACC[A/G]AGCAACTTGGGTCAC	80176
rs759963317	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9300691	CCGACCAAACCAGAC[A/G]TTGGGCATGTGTGGC	80176
rs760057243	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9317549	GGACAAAGCTCACTG[C/T]GGCTTCTGCCTCCCA	80176
rs760067366	in-del	-/A			intron-variant	SPSB1	GRCh38.p7	1:9314195	AAAAAAACAAAAAAC[-/A]AAAAAAAACAGTGAA	80176
rs760081283	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9331094	CTTTCATATTCTGTC[A/G]TGCTCTCCCCGCTGA	80176
rs760088144	snp	C/T			utr-variant-3-prime	SPSB1	GRCh38.p7	1:9368247	AAACCCTGTTTCAGT[C/T]CCCTCTCTCTGGCTG	80176
rs760167062	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9366524	TGGATTCAGATCCCA[G/T]CCCTGAACCTTGGCA	80176
rs760185301	in-del	-/TC			intron-variant	SPSB1	GRCh38.p7	1:9294273	ACACGTGTCTCTGTG[-/TC]TGTCTCTGTGTCTGT	80176
rs760186222	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9301048	CCTGGCAGAGCTTCG[C/G]GCAGTGCACCTGGTT	80176
rs760250128	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9341521	ATTATTTGGACTTGG[A/G]TGTTTTCCCACTGTT	80176
rs760275208	in-del	-/G			intron-variant	SPSB1	GRCh38.p7	1:9314853	AGGAGGCACAAATGA[-/G]GGAGGCAGCCAGTGG	80176
rs760410185	snp	A/G	1.87236e-05	0.00305965	missense	SPSB1	GRCh38.p7	1:9367555	CCGGCTTCCCTCAAG[A/G]CCTACCTCCTCTACC	80176
rs760417367	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9350325	GTTTGGTGGGGCAGG[A/T]GGGGTACAGGCCAGG	80176
rs760521346	in-del	-/AC			intron-variant	SPSB1	GRCh38.p7	1:9350101	ACGCCTCACATATCT[-/AC]ACACACACACACACA	80176
rs760549478	in-del	-/TT			intron-variant	SPSB1	GRCh38.p7	1:9303409	ATACCAGCTCCAACC[-/TT]ACGTGACCAGTTACA	80176
rs760569884	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9336387	ACGCACCACTATGCC[C/T]GGCTAATTTTGTATT	80176
rs760597307	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9360137	CTGCCACCCTGGGTG[A/T]GGTCACCAGAAGTAG	80176
rs760625561	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9326130	GTGGGGAGGTCGGGT[A/G]GAATGTTCTTGGTGG	80176
rs760687747	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9320177	CCTCCTAAATTTGCA[C/T]GGCAGAAACTTCCTT	80176
rs760717112	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9363356	GCCACTTCTCTAGCC[C/T]GTCTTGGTGGATCCC	80176
rs760717493	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9344246	CTCATTAGAATGCAG[A/G]CTGCCCCGTGGAGTT	80176
rs760752754	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9313443	AAATAAAATAACTTG[C/T]CCAGGGCTGCACAGC	80176
rs760769135	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9335822	GTGAAAAAAAGAAAG[A/G]AAGAATGTTGTGGTT	80176
rs760853960	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9307110	TTTTTGTATTTTTAG[C/T]AGAGATGGGGTTTCA	80176
rs760854943	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9330124	GCGTAAATAATTGCT[A/T]GGTGCTTGCTCATCG	80176
rs760866136	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9294508	CCCTGCTGGTGCCCC[C/T]GAGGAGAGCGCAGGC	80176
rs760886109	snp	C/T	5.06513e-05	0.0050322	synonymous-codon	SPSB1	GRCh38.p7	1:9356101	CTTTGTGAAGGAGGA[C/T]GACAAGCTCATCTTT	80176
rs760897889	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9319034	TACAAAAAAATTAGC[C/T]GGGCATGGTGGCGCA	80176
rs760916624	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9295085	TGGGCCAGGCACTTC[A/G]TGTCTCCCCAGCTGT	80176
rs761006249	in-del	-/T			intron-variant	SPSB1	GRCh38.p7	1:9347945	AGTTTCCCTGCAACT[-/T]TTTTTTTTTTTTTTT	80176
rs761012033	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9306693	CCACAAAAGAGGAGC[A/G]AGGAAGAAATGAGCG	80176
rs761028796	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9345896	TCAAGTTGGCAGTTG[G/T]CAGGGTGAGGGGTGG	80176
rs761074806	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9346882	GTAGAGAGAGACAGC[C/T]GCCCCATTTTTACGG	80176
rs761117186	snp	G/T	0.000167566	0.00915177	synonymous-codon	SPSB1	GRCh38.p7	1:9356530	ACTGTATCCTGTAGT[G/T]AGTGCCGTCTGGGGC	80176
rs761125856	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9323278	TTCCCGCCGAGCCGA[C/G]GGGGGCTGTGGCTCC	80176
rs761126888	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9332671	GGCGGAGGAGCTGAG[A/G]CAGAACCTTAGAGAG	80176
rs761195965	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9357827	CCTGGCGTTGCAGAA[C/T]GGCTCACCCCGTGTA	80176
rs761214097	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9305249	GGCCCATACCCTCTC[A/G]CTTCACTTTCCAAAA	80176
rs761286326	in-del	-/CGCGCCC			upstream-variant-2KB	SPSB1	GRCh38.p7	1:9292732	CGGGCTGACGCGCCC[-/CGCGCCC]CGCGCCCCGCGCCCC	80176
rs761307867	snp	A/G	1.76789e-05	0.00297307	synonymous-codon	SPSB1	GRCh38.p7	1:9367542	CACGCTGCCGCTGCC[A/G]GCTTCCCTCAAGGCC	80176
rs761362730	snp	C/T	4.99189e-05	0.00499569	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9367609	CAGCGCGACAGCCAC[C/T]TGGTGCCAACTCACT	80176
rs761402138	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9323450	GGATGTCAGAGGGTG[C/G]TCAGCCTGGCACTGG	80176
rs761402723	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9366730	AGGCACACACCACCA[C/T]GCCCAACTAATTTTT	80176
rs761416841	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9302143	TGGAACTACGGTCTT[C/G]TTATTGCCTTTATTT	80176
rs761424178	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9333796	GCCCACGGGCCAAAT[C/G]AATAGCAACATTCTC	80176
rs761471329	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9344400	CTGCCTTTCCTCACC[A/G]CCAGACAGAGGGAGG	80176
rs761520068	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9332734	TTCAGGTCAAGGGCA[C/T]GGTGGTATTTTCAGA	80176
rs761609680	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9341653	TGTTTTCTAGCAGTT[C/T]GGAGGAAGGCCTGTT	80176
rs761621631	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9310356	GTGAGGTTCTTGGGG[C/T]GCCTTCCTGGATTTC	80176
rs761659977	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9353467	GATTTTCCTGGGAGA[G/T]CATGGATGTGAGGTC	80176
rs761696277	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9327680	CCCCTGTTTCTTCAC[A/C]ATTTCCTAAGGTCTC	80176
rs761758184	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9350574	GCACACAGTGTACAC[A/G]TGTGTGCATGTGTGT	80176
rs761778603	snp	C/T			upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291848	CCACTCAGGCCCGCC[C/T]AGCCCAGGGCAGTTG	80176
rs761797171	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9343649	GGGCTCCTTTCTACC[C/T]CTTTCCTGAGTATGC	80176
rs761856094	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9337256	ATTAGCTCCAGCTCA[A/T]TGGCCTTCCCCCTCC	80176
rs761891168	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9354206	ATTTCCGTGTGTCTG[C/G]GAGCCTGCAGCCTCC	80176
rs761968840	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9338051	GGGGTGCAGGGAAGA[A/G]GGAGCAGGTTTGAAT	80176
rs761992725	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9297888	AAGACAGATCTTTCA[C/T]GCATACGTTGAGAAA	80176
rs761993029	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9365556	TATCCAATTCAGTGG[C/G]CTCTTGCGTGGTGAG	80176
rs762080507	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9307684	CCTGTCTTTCTGTCC[A/G]TATCCCTCATCACCA	80176
rs762095462	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9329632	CAGGATGGGGAGGTT[A/G]CAGTGAGCCGAGATC	80176
rs762098980	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9353216	CCTCGAGAGCCGCCT[C/T]GGCCCTCCCAGCCTT	80176
rs762108525	in-del	-/TGTG			intron-variant	SPSB1	GRCh38.p7	1:9348940	ACTCGTGCAAGAATG[-/TGTG]TGTGTGTGTGTGTGT	80176
rs762128972	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9364633	TTCATTCCTCCATTC[A/G]TCTCCAATCAGAGCT	80176
rs762161189	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9338144	CCCTGTCCCCTCGCT[C/G]CTCCCCCCAGACCTG	80176
rs762219938	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9330731	TAATCGTGGTAAAAC[A/T]TACAAAAACCTAAAA	80176
rs762248858	snp	A/G			utr-variant-3-prime	SPSB1	GRCh38.p7	1:9367948	CCTGGGGGTCCCAGG[A/G]TGGTGGGGGTGGCAG	80176
rs762295888	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9324646	CCAGTGGCCAGCCTG[A/T]CTTGTTCCTATAAAG	80176
rs762318129	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9358716	CCTGCCCACTGAGAC[C/T]GTGGGGCCCCATGAA	80176
rs762326307	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9347181	AAAGCGTTTTAAACG[C/T]CCTTCTACCAGTTAT	80176
rs762332316	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9347461	TTTTTCCCTCCCACC[C/G]ACAATCATTAACCAT	80176
rs762450380	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9316388	GGGGCATGTGTGCAC[A/G]TGTATTTATGTGTGT	80176
rs762520370	in-del	-/GTGTGC			intron-variant	SPSB1	GRCh38.p7	1:9295238	TGTGTGTGTGTGTGT[-/GTGTGC]GCGCGTGCGGTTGGG	80176
rs762524481	snp	C/T	1.73881e-05	0.00294852	missense	SPSB1	GRCh38.p7	1:9367535	AGATCCACACGCTGC[C/T]GCTGCCGGCTTCCCT	80176
rs762562280	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9325878	CCCGGTGTGCCCAGA[A/G]CCAGGCAGAGGACTT	80176
rs762619131	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9328948	AAATCTCCCAGGGTA[C/T]GCTGGGGTGAAGGAG	80176
rs762626117	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9334937	CATTTTGCTTCTTTG[C/T]TCATCTGTCCGTGGA	80176
rs762629436	in-del	-/AG			intron-variant	SPSB1	GRCh38.p7	1:9320242	AGCATTGTTCTAGGC[-/AG]GGGGTTGCAGCTCGA	80176
rs762653900	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9324867	GCCGTGGAGCCAGCA[C/T]GGTCTTGTCGGATCC	80176
rs762654313	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9302213	TATGGGTGCCAGTTG[G/T]TAAGGGGTGGACCTG	80176
rs762669083	snp	A/G			utr-variant-3-prime	SPSB1	GRCh38.p7	1:9368721	AGCCGGGGGCAGGGT[A/G]GGATGGGGAAGACCA	80176
rs762699709	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9344533	GGCATTCACGATTCC[A/C]AGCTATCAGGTGTCC	80176
rs762864666	in-del	-/GAAGAGCAGGG	1.78217e-05	0.00298505	frameshift-variant	SPSB1	GRCh38.p7	1:9367544	GCTGCCGCTGCCGGC[-/GAAGAGCAGGG]TTCCCTCAAGGCCTA	80176
rs762885922	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9363188	GGAAAGCAGTTAGAC[C/T]GGGCCCTATGCGCCA	80176
rs762886345	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9341724	TTTGTTTTTTTGAGA[C/T]GGGGTTTCACTCTTG	80176
rs762892241	in-del	-/A			intron-variant	SPSB1	GRCh38.p7	1:9343362	ATCGTACAATGTGTG[-/A]ACCTTTTATATCTGG	80176
rs762899598	in-del	-/T			intron-variant	SPSB1	GRCh38.p7	1:9322676	GAGGCCAGGACCACC[-/T]TGCAGGTTCCACTGT	80176
rs762933717	snp	C/G	1.65241e-05	0.00287433	missense	SPSB1	GRCh38.p7	1:9356320	GTCCTGGGGCTGGGA[C/G]TTGGGGCGCAACCGG	80176
rs762961356	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9332695	TAGAGAGTGAGTCAG[A/T]TACTGTCACAAAACT	80176
rs763023977	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9344288	AAGTCTAACGGGATC[A/C]GGAATTTGCATCTCT	80176
rs763098283	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9308896	GCACAGCTTGGGAGG[C/T]GTGTGATGCACCTCC	80176
rs763121892	snp	A/G			utr-variant-3-prime	SPSB1	GRCh38.p7	1:9368118	AAGGCAGAAACCAAG[A/G]ACTGTCTGCAGGCAA	80176
rs763129974	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9304769	GCAACTGGGCTCAAC[A/G]CTCAAGCAATCCTCC	80176
rs763139286	snp	A/G	1.64868e-05	0.00287109	missense	SPSB1	GRCh38.p7	1:9356444	GCCCTGGACATGGAC[A/G]ACGGGACTCTGAGCT	80176
rs763276499	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9321894	GGAATATGACAGCAG[C/T]AAGATTAATACCCGT	80176
rs763300998	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9330375	GAGGCTGAGGCAGGA[A/G]AATCGCTTGAACCCG	80176
rs763402027	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9354282	CACCCTAGTAACAAG[C/T]GACCCAGCGTGACTC	80176
rs763470690	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9338783	GGGTGGCGTGGGCCA[C/T]GATTCTGCCTTCGCC	80176
rs763494618	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9322750	GGCAGGTGTCGGAGA[A/G]GGATGTTGACTTGGA	80176
rs763552487	snp	A/G	1.66197e-05	0.00288263	missense	SPSB1	GRCh38.p7	1:9367478	TCATGGATTTGTGCC[A/G]TCGCTCGGTGCGCCT	80176
rs763587653	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9310066	TCAGGTGGGGGATGG[C/T]GAGGGGCCTGTGATG	80176
rs763615522	in-del	-/ACACAGATACAT			intron-variant	SPSB1	GRCh38.p7	1:9350073	CCAGACACACCACAC[-/ACACAGATACAT]ACACGCCTCACATAT	80176
rs763619871	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9317417	GGATTTGGTTTAGGT[A/G]TCTGGGAGAAGGGGT	80176
rs763653567	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9302048	AGCTCACTTCACAAC[C/G]AAGGAAGTGTGGCAC	80176
rs763669519	in-del	-/GAA			intron-variant	SPSB1	GRCh38.p7	1:9301078	TGTGCACCTTGCTTC[-/GAA]GGAGAGATGGCCAGA	80176
rs763681516	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9301020	TGAAGGATGGGGGTG[A/G]AGGGAAATCCTCCCT	80176
rs763732105	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9365516	TGAGCTATAATTCAC[A/G]TACCTTACAATTCAC	80176
rs763773115	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9300276	ACTTTGGAGGCAACA[C/T]ATTCCTCATTTGGGT	80176
rs763825663	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9350964	CTGTCTTGGTCCAGT[A/G]TTAACAGGAGCCATC	80176
rs763855373	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9340826	CAGCCTGTCTGATGT[C/T]GCGGAGCAGCTCTGC	80176
rs763856037	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9317627	GGTATGCACTACCAC[A/G]CCCAGATATATATAT	80176
rs763864714	snp	C/T			upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291730	TCCAGCCTCAAGTGA[C/T]CTTTTAAATGGGAAG	80176
rs763931117	snp	A/G	1.6808e-05	0.00289892	missense	SPSB1	GRCh38.p7	1:9356094	TCAATGTCTTTGTGA[A/G]GGAGGACGACAAGCT	80176
rs764006156	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9361081	TGTCCTGGTGAGATC[A/G]AATCCCAGGGTCTGC	80176
rs764026402	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9336388	CGCACCACTATGCCC[A/G]GCTAATTTTGTATTT	80176
rs764029534	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9349588	TGGACGGCTTGCCTG[C/T]CTTCCTCAGGAGGAA	80176
rs764065144	snp	A/C	0.000166522	0.00912324	intron-variant	SPSB1	GRCh38.p7	1:9367404	CGCTGTTTGCTGAAC[A/C]CCCACCCAAGCTGCG	80176
rs764102209	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9309186	CCTTGCACTTCCATG[A/C]CATTCACCTCCAAAG	80176
rs764161320	in-del	-/GTG			intron-variant	SPSB1	GRCh38.p7	1:9295236	TGTGTGTGTGTGTGT[-/GTG]TGTGCGCGCGTGCGG	80176
rs764217071	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9353111	CTGGGCACCAAGCTG[A/G]AGGGGGTGTCCAGAC	80176
rs764272019	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9351894	TGTGTGGGCCACATT[C/G]CCTGGCTAGGCCCTG	80176
rs764318382	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9362581	GGGCATTCTCTGATG[C/T]GGAACATTTTTCCTT	80176
rs764318774	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9338008	TCTGAAAAAAGGCAG[G/T]GATGGAGATGTCCCC	80176
rs764406678	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9347171	AAAAGAAAAAAAAGC[A/G]TTTTAAACGCCCTTC	80176
rs764427848	in-del	-/A			intron-variant	SPSB1	GRCh38.p7	1:9321658	GCTTCACCTTTAAAT[-/A]AAAAAAAAAAATGCT	80176
rs764435819	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9306707	CGAGGAAGAAATGAG[C/T]GATCCGAGAGATAGG	80176
rs764489587	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9327967	CTCAGTTTCTCACCA[A/G]AGTGCAAGCCGCTGA	80176
rs764492440	snp	A/G	1.7565e-05	0.00296347	synonymous-codon	SPSB1	GRCh38.p7	1:9356218	GGCCATGAGACAGCG[A/G]GGCACACACGCCGTG	80176
rs764591788	in-del	-/GGGTGG			intron-variant	SPSB1	GRCh38.p7	1:9360207	GCTTAGAGGCCAGGA[-/GGGTGG]GGGTGGGGGCTGAAG	80176
rs764621341	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9316390	GGCATGTGTGCACGT[A/G]TATTTATGTGTGTGC	80176
rs764712769	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9323470	CCTGGCACTGGGTAC[C/G]AAGGCTGACCTTGAA	80176
rs764730875	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9302168	TTATTTGGAAATTAA[A/G]TATGGTTTAAGAAGA	80176
rs764780961	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9324672	TAAAGGGCACTTTGT[A/G]TGTGGCTCCTGGCAG	80176
rs764782492	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9357888	GAGTCCCTTCTACCG[C/T]CTGCAAGTCCCACGT	80176
rs764821197	snp	C/T	1.85493e-05	0.00304537	intron-variant	SPSB1	GRCh38.p7	1:9356634	CTCCCTCAGTCCCCA[C/T]GGTCCTGGCTGGGCT	80176
rs764834979	snp	A/C/G	4.98652e-05	0.00499305	synonymous-codon	SPSB1	GRCh38.p7	1:9367461	AGCCGAGCCGCTGCC[A/C/G]CTCATGGATTTGTGC	80176
rs764937181	in-del	-/A			intron-variant	SPSB1	GRCh38.p7	1:9296850	ACAGCACATTGGGGG[-/A]ATCTGTCCTGCTGCC	80176
rs764964731	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9301128	ATCCATGGGCTGTGC[C/T]TGATGATTTGGCTGG	80176
rs764988193	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9332797	TTTTGGGCCCGTTCA[A/G]TTTATCGATTAGGAG	80176
rs765058635	in-del	-/TC	1.66396e-05	0.00288436	intron-variant	SPSB1	GRCh38.p7	1:9367433	CGCTGACCTGCAGTT[-/TC]TCTGTCTCCCCAGCC	80176
rs765079807	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9331928	TTGCATTGTCTGTTC[C/T]AGTCCTCTGGCTATT	80176
rs765079931	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9341674	AAGGCCTGTTCTCCC[G/T]TCCTGAACGGTGACC	80176
rs765087292	in-del	-/T			intron-variant	SPSB1	GRCh38.p7	1:9293875	GTGTGTTTGTGCATG[-/T]CCTTGTGAATATGTG	80176
rs765089175	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9327766	CCATATGGTGTCTGC[C/T]GCAACTACTCGACTC	80176
rs765142877	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9351526	GTGGATCTTGGTGGC[C/T]GGAGCTACTGTCTCG	80176
rs765232733	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9295115	TGAAGTGATGGGCTG[C/G]ATTAGATCATTTAAA	80176
rs765252246	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9335213	GTGCCTCAAAAGAAT[G/T]TTGTGGGGTTAGGCA	80176
rs765315110	snp	A/T			upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291916	GCTAAACCAAACTGA[A/T]TTTCAGCACCGTAAA	80176
rs765332231	in-del	-/ACCA			intron-variant	SPSB1	GRCh38.p7	1:9319242	CTGGGAAGTGGGGGG[-/ACCA]GGGGGGTGGCACAGG	80176
rs765353264	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9303651	TAGCACTCAAGGACT[C/G]TACCTCCTCTCTGGA	80176
rs765364976	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9342764	TACAGGTGCTGTCTC[A/G]GGGCAGCAAGGGCTG	80176
rs765365498	snp	C/T			downstream-variant-500B	SPSB1	GRCh38.p7	1:9369823	GTGATTCTGTGCCTT[C/T]GTGAGCGCATCAGGT	80176
rs765376540	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9313446	TAAAATAACTTGCCC[A/G]GGGCTGCACAGCCAA	80176
rs765392617	in-del	-/CTTTTCTT			intron-variant	SPSB1	GRCh38.p7	1:9306914	GTCTTTTTTCTTTTA[-/CTTTTCTT]CTTTTCTTCTTTTTT	80176
rs765400282	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9343657	TTCTACCTCTTTCCT[G/T]AGTATGCCGATACAG	80176
rs765431013	in-del	-/GTG			intron-variant	SPSB1	GRCh38.p7	1:9348959	TGTGTGTGTGTGTGT[-/GTG]TGTATATGTGCGTGT	80176
rs765478472	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9353271	TGGAGGTTGGGGAAG[A/C]GGGGAATTCAGGGAA	80176
rs765497452	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9312886	CCAGAGGCAGTGCGT[A/G]CCGATTGTCCAAAGC	80176
rs765498851	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9330299	ACGGTGAAACCCCGT[C/T]TCTACTAAAAATACA	80176
rs765583689	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9296126	GAGTGCTTTATGGAC[A/G]TGACTTTGTTTGAAT	80176
rs765590743	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9338691	GGCCTTGCAGGCAGG[A/G]CTGGGGTCTTCAGTG	80176
rs765618736	in-del	-/TGGG			intron-variant	SPSB1	GRCh38.p7	1:9357145	GAGTGGATGGATGGA[-/TGGG]TGGGTGGATGGATGG	80176
rs765657760	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9364640	CTCCATTCGTCTCCA[A/G]TCAGAGCTCCTCTTA	80176
rs765675727	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9307219	AGGCATGAGCCACTG[C/T]GCCTGGCCGTCTTTT	80176
rs765791220	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9338152	CCTCGCTCCTCCCCC[C/T]AGACCTGGAGACATG	80176
rs765803646	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9316768	AGCGGCATTGGGTCT[A/G]GGTCTGGGGGCCGCA	80176
rs765833107	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9338821	CCTGGGGGCGCTCCC[A/G]CCTTGCTCTGCTGTG	80176
rs765900377	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9344570	AGCCTCAGGTGTTGA[A/G]AGGCGGCAGGAGGAG	80176
rs765920181	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9359035	GTGAGTGGGGAATAC[C/G]AGAATGGGAATCAGG	80176
rs765972242	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9311431	GCAGAGTAGAGAGAC[G/T]GGTGTCCTGAACCCC	80176
rs766006284	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9326339	TGGAGACACCCAGGG[A/G]CCACTCAGACTGGGC	80176
rs766063448	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9320573	TTGTTCCTTGATACA[C/G]AGAGGAAGCACGCAG	80176
rs766124759	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9332983	CATCCTGGGCTCCGT[A/G]GCTGAGACTTGGTTT	80176
rs766160128	snp	C/T	1.89784e-05	0.0030804	missense	SPSB1	GRCh38.p7	1:9367556	CGGCTTCCCTCAAGG[C/T]CTACCTCCTCTACCA	80176
rs766176707	snp	C/T	1.68335e-05	0.00290111	synonymous-codon	SPSB1	GRCh38.p7	1:9356536	TCCTGTAGTGAGTGC[C/T]GTCTGGGGCCACTGT	80176
rs766210948	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9341764	CTGGAGTACAATAGC[A/G]CGATCTCGTCTCACC	80176
rs766227680	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9323835	GCTGTTGCCCACGGA[C/T]GGCAGGGGCTGTGCC	80176
rs766229917	snp	C/T			utr-variant-3-prime	SPSB1	GRCh38.p7	1:9369122	TTTTTAAGTAAATCT[C/T]ACAGTGGAGTATATT	80176
rs766286180	snp	A/G			utr-variant-5-prime	SPSB1	GRCh38.p7	1:9292940	CTCGCAGCAGGAACC[A/G]GGCTCCAGGCGCCGG	80176
rs766287186	snp	C/T			utr-variant-3-prime	SPSB1	GRCh38.p7	1:9368079	AGATAAAGCTCAGGA[C/T]GTCAAAAACTCACCA	80176
rs766362265	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9308954	GGTGTATGCAGGAAA[C/T]ATGAGCTCCCTGCCA	80176
rs766384598	snp	A/G	5.06436e-05	0.00503182	missense	SPSB1	GRCh38.p7	1:9356102	TTTGTGAAGGAGGAC[A/G]ACAAGCTCATCTTTC	80176
rs766432426	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9326908	AGCTGGCGCCTTTTT[G/T]AGGTGGAGGCGGGGA	80176
rs766492008	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9360412	CTGATGGAGTGGCTG[A/G]AGGAAGACAGACAGG	80176
rs766518302	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9336530	CACGTCCGGCTCCTC[C/G]TCCTGGTTCTTTACT	80176
rs766526215	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9335384	GTGAGCACCTGTAAT[A/C]CCAGTTACTCAGGAG	80176
rs766566155	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9305784	TGCAGCCAGTCTGCT[A/G]GGGCCGAGGATACAA	80176
rs766616253	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9343817	TTGAGACAGAGTCTC[G/T]CTCTGTTGCCTAGGC	80176
rs766628507	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9321908	GCAAGATTAATACCC[A/G]TAGGTGCCATTGACG	80176
rs766637061	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9307868	TGTGGTCTTCGGGGT[A/G]CGCGTGGCCCCTCCC	80176
rs766691929	snp	C/T	1.76658e-05	0.00297197	missense	SPSB1	GRCh38.p7	1:9356199	ACGTGTGGCAGATCA[C/T]GTGGGCCATGAGACA	80176
rs766750799	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9331243	CAATGACTGTGCACT[C/T]GATTTGGAGTGGCAG	80176
rs766770683	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9302283	AATACCCAGGTAGAT[A/G]GTAAAGCATTGATTA	80176
rs766778793	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9355552	ACAGACAGACCCTTT[C/G]CTTTGTGACAGCTAG	80176
rs766796245	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9359686	TAGCCTGGGCAACAG[A/G]GCAAGACTCCGTCTC	80176
rs766803288	snp	C/T	3.69004e-05	0.00429521	intron-variant	SPSB1	GRCh38.p7	1:9356625	GGCAATGCCCTCCCT[C/T]AGTCCCCATGGTCCT	80176
rs766821535	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9296529	TCACCTCGCATGCAC[A/G]CACATACACATACTC	80176
rs766838508	in-del	-/TTA			intron-variant	SPSB1	GRCh38.p7	1:9312741	GGTTTTCTTTGGGTT[-/TTA]TTATTATTATTATTT	80176
rs766873205	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9316575	GGGGGCTGATCGAAG[C/T]GGGTTCAGGGGCTGC	80176
rs766881176	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9339654	GAGGGCCTGTCAGGG[A/G]CTTGGAAGGTGGAGA	80176
rs766915208	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9332682	TGAGACAGAACCTTA[C/G]AGAGTGAGTCAGATA	80176
rs766929584	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9298247	TCTGTATAAGCAGAA[A/G]CTTACAGGTCAAATG	80176
rs766943922	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9364901	CGTCACCCCAGGCTG[A/G]AGTGCGATGGTGTGA	80176
rs766961168	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9331127	GCTTGTGGAAGTGTC[G/T]CCAGGCTCACTGATG	80176
rs766976638	snp	A/C/G			intron-variant	SPSB1	GRCh38.p7	1:9339711	GCCTCCAGCAGGGTC[A/C/G]CCCTGACCTCTGTCT	80176
rs767007167	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9365376	CTGTCCTTGGCCTCC[C/T]AAAGTGCTGGGATTA	80176
rs767062603	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9349448	GGGGCTGTCCCAGCT[A/G]AGCTCAACCAGAGAG	80176
rs767082985	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9313871	ATCTCCTGCTTTTCC[C/T]TATAGGAGTGAACAA	80176
rs767129036	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9308909	GGCGTGTGATGCACC[A/T]CCAGGCCCCTGAGAG	80176
rs767180234	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9300923	CCTGGTTTGCAGATG[A/G]CTACAGATGGCTCTG	80176
rs767184737	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9338954	AACCCGGCCGATTAC[C/T]TTGTAATTGTTCCCA	80176
rs767217127	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9308066	GGTGCCCCTTCCAAA[C/T]CCTGTTAACCCGTCT	80176
rs767274536	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9348366	GCTGTATCCAGAAGG[C/T]GCTCTCTGACCACAG	80176
rs767279363	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9325094	AAGCTGGGACTCCAG[A/T]GCTCAGCACGTGGAG	80176
rs767279720	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9307990	TCTGTAACTCATGGT[A/G]CTCCTCCTCCTGGGG	80176
rs767313240	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9317569	TCTGCCTCCCAGGCT[C/T]GGGGATCCTCACACC	80176
rs767325634	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9326062	TGTCCCACTCCACCC[C/T]TGCATGTCCCTTAGT	80176
rs767375486	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9312694	ATTGGATGATTGTGC[A/G]TGGACTCATCTCATC	80176
rs767382616	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9360081	CCTAGTCTCAGAGAG[A/C]GGTCAGTGGGGGAGT	80176
rs767395717	snp	A/T	1.79027e-05	0.00299183	synonymous-codon	SPSB1	GRCh38.p7	1:9367545	GCTGCCGCTGCCGGC[A/T]TCCCTCAAGGCCTAC	80176
rs767430193	in-del	-/C			intron-variant	SPSB1	GRCh38.p7	1:9339998	GACCCCCACCGACAG[-/C]CCCTGAACCACCTGG	80176
rs767437507	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9359108	CAGAGCATCACAGCC[A/G]GGCGCTATTAGTCAG	80176
rs767476979	snp	A/G	1.66203e-05	0.00288268	synonymous-codon	SPSB1	GRCh38.p7	1:9367485	TTTGTGCCGTCGCTC[A/G]GTGCGCCTGGCCCTG	80176
rs767507967	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9302435	GACACTGGCAATTGA[A/G]TCACTCAACTGGGTG	80176
rs767510667	in-del	-/T			intron-variant	SPSB1	GRCh38.p7	1:9321670	AAATAAAAAAAAAAA[-/T]GCTGCTGATTGTCAC	80176
rs767600577	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9362425	CTGCGTAGTGTAGAG[A/G]AAAACACACACACAT	80176
rs767602582	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9350708	AGCCACGCCCTTTGC[A/G]TCTGCTCCTCCTGGG	80176
rs767609982	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9319538	GCCACTGTGCTCCCC[A/G]CTGAAGTCGAGTGGA	80176
rs767615567	snp	A/G			utr-variant-3-prime	SPSB1	GRCh38.p7	1:9368262	CCCCTCTCTCTGGCT[A/G]TTCTGTTACTTTCCT	80176
rs767653133	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9305982	ACCTGGGGACATTTG[A/T]GCAATTGCGAGTAAC	80176
rs767689053	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9294842	CCTCCTCAGACCCCC[C/T]TCCCAGTGGTGGAAA	80176
rs767725423	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9361624	AGTTCTCGACGTTTC[C/G]CTGTGCGGCCTCCCC	80176
rs767731224	snp	C/T	1.65064e-05	0.00287279	missense	SPSB1	GRCh38.p7	1:9356333	GACTTGGGGCGCAAC[C/T]GGCTCTACCACGATG	80176
rs767779137	snp	C/T			upstream-variant-2KB	SPSB1	GRCh38.p7	1:9292137	AGGCTAACTCCTCAC[C/T]GTTTTCAATGGACAC	80176
rs767791256	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9349059	CAAACCCCAGGGCTT[C/T]GTGTCATCTGGTGTC	80176
rs767838223	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9363051	AGTCAAGAGTGTGGA[A/G]GTTGGGGAGAACTCC	80176
rs767865217	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9337453	GTTCACTCGTTTTAA[C/T]TTTAAGGCCTCCATG	80176
rs767887377	in-del	-/GT			intron-variant	SPSB1	GRCh38.p7	1:9295193	CCCAGTAGATGGAGT[-/GT]GTGTGTGTGTGTGTG	80176
rs767891834	snp	A/G	1.64993e-05	0.00287218	missense	SPSB1	GRCh38.p7	1:9355998	ACTGCAAGCCCACCC[A/G]GCTGGATCTGCTACT	80176
rs767920469	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9350611	AGGCATGCGTGCATG[C/T]GTGTGTGTGGTGGGT	80176
rs767924063	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9322682	CAGGACCACCTGCAG[G/T]TTCCACTGTGGCTGG	80176
rs767986623	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9314018	CCTTTTCCACTAAAA[A/G]TACAAAAATTAGCCA	80176
rs768006565	snp	A/G	1.66363e-05	0.00288407	synonymous-codon	SPSB1	GRCh38.p7	1:9356515	ACTCAAGGGCAAAAA[A/G]CTGTATCCTGTAGTG	80176
rs768041169	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9344577	GGTGTTGAGAGGCGG[C/T]AGGAGGAGGGCAGGG	80176
rs768071229	in-del	-/G			intron-variant	SPSB1	GRCh38.p7	1:9361794	TGGCCATTGCTGAGT[-/G]GGGGAGACACAGGGC	80176
rs768074404	in-del	-/T			intron-variant	SPSB1	GRCh38.p7	1:9318978	GCACATCACCTGAGG[-/T]CATGCCTGGGCAACA	80176
rs768088315	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9335685	CATTCCTGTAGTCCC[A/G]GGTACTTGGGAGGCT	80176
rs768097316	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9304371	CGATGAGCCAGTTCC[C/T]CTAACCCATCCTTTC	80176
rs768165627	snp	A/G	5.22981e-05	0.00511335	synonymous-codon	SPSB1	GRCh38.p7	1:9367536	GATCCACACGCTGCC[A/G]CTGCCGGCTTCCCTC	80176
rs768184249	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9300194	CCCCTCTAAGGTGAA[A/G]AATAAGTTGTTACAG	80176
rs768319468	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9352052	CCATCCCTCACAGCC[A/G]TGTGGTCCAAGGCCT	80176
rs768326865	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9328325	TCCAGGAAGAATGTC[C/G]CTTTTCTTCAAGTTT	80176
rs768338858	snp	A/T	1.7668e-05	0.00297215	missense	SPSB1	GRCh38.p7	1:9356193	GGCTGCACGTGTGGC[A/T]GATCACGTGGGCCAT	80176
rs768353208	in-del	-/GAT			intron-variant	SPSB1	GRCh38.p7	1:9356818	GATGGATGGATGATG[-/GAT]GATGATGAATGAATA	80176
rs768363537	snp	A/G	0.000116702	0.00763789	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9367600	TCATACCGCCAGCGC[A/G]ACAGCCACCTGGTGC	80176
rs768368992	in-del	-/TTA			intron-variant	SPSB1	GRCh38.p7	1:9312743	TTTCTTTGGGTTTTA[-/TTA]TTATTATTATTATTT	80176
rs768410523	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9327572	TGAGCACTTGTCTGT[A/G]CTTGGGGAGCAGCTG	80176
rs768414773	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9337779	TCCCTGCCTCCGTTC[A/G]TTCTCTTGCTCCCTC	80176
rs768489271	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9327139	GTGCCCACTTGCAGC[A/G]CTTCCGGGGGTCCCA	80176
rs768500498	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9337184	TGGTTGTCCTAGAAA[C/T]GGTCCATTTATGTTA	80176
rs768532497	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9311149	GGTGTCTAGACAGCG[C/T]AGGATAAAGGGTTTT	80176
rs768569445	snp	C/T	6.59587e-05	0.00574239	synonymous-codon	SPSB1	GRCh38.p7	1:9356446	CCTGGACATGGACGA[C/T]GGGACTCTGAGCTTC	80176
rs768645858	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9315883	AAACAAAACAAAACA[A/G]AACAAAACATGGAGT	80176
rs768663908	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9362785	GTGGAAGCTGGTGCA[C/T]TGTCTCTTCCAGTTC	80176
rs768677942	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9364478	TCCAGGTCAGGCTGC[A/G]GGGCAGGGTCTGGAG	80176
rs768697705	snp	C/T	0.000170783	0.00923916	synonymous-codon	SPSB1	GRCh38.p7	1:9356254	GGTGGCGACGGCAGA[C/T]GCCCCCCTGCACTCT	80176
rs768705952	in-del	-/T			intron-variant	SPSB1	GRCh38.p7	1:9336253	TTTTTTGAGATGGAG[-/T]TTTCACTCTTGTTGC	80176
rs768711226	in-del	-/T			intron-variant	SPSB1	GRCh38.p7	1:9317699	CTATTGCCAGGCTGG[-/T]CTCAAACTCCTGAGC	80176
rs768737666	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9314841	CCGGGGTCAGGAAGG[A/G]GGCACAAATGAGGGA	80176
rs768783775	snp	C/T	3.58757e-05	0.00423516	missense	SPSB1	GRCh38.p7	1:9356585	TTGAACGGACTCGAT[C/T]GTAAGTGTCTCCTCT	80176
rs768916017	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9317158	TTAGAGGCCAGCAAG[G/T]TTCTGGCCTTGGGGA	80176
rs768919545	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9330139	AGGTGCTTGCTCATC[A/G]AGAAGAATCTGAATG	80176
rs768986685	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9324563	GGGTGGGGAGGGGGA[A/G]TCAAGACAAAAGCCT	80176
rs769040914	snp	A/T	1.74233e-05	0.0029515	synonymous-codon	SPSB1	GRCh38.p7	1:9355924	TGGAGGGATCAAGAC[A/T]GTGGACATGAGGGAC	80176
rs769061766	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9325683	TCTCACAGGGGACGG[A/G]TCTTAAGCAGATAAC	80176
rs769073635	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9358645	GGAGCCAGGGAGGTT[A/C]ATGTCCATTCTTTGC	80176
rs769078485	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9333652	TCAGCTTCCTGAAGC[A/G]CCTGCGGTGTGAGCC	80176
rs769128578	snp	C/T			utr-variant-3-prime	SPSB1	GRCh38.p7	1:9368621	TCTAGCTGAGATTTC[C/T]CAAGTGCATCCTCAG	80176
rs769128786	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9357828	CTGGCGTTGCAGAAC[A/G]GCTCACCCCGTGTAC	80176
rs769151536	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9334749	TTCAACTTTCTGTCT[C/T]TATGGATCCGATTGT	80176
rs769168697	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9365111	ATGCGCCGGCCTCGG[C/T]CTCCCGAAGTGCTGG	80176
rs769227170	in-del	-/TGTGTC			intron-variant	SPSB1	GRCh38.p7	1:9294043	CTGTGTGTGTGTGTG[-/TGTGTC]TGAGTGCGTCTTTGT	80176
rs769246629	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9302779	TCTTCAAAAGGCTCT[A/G]TGTACTCTGTATCAG	80176
rs769284065	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9313169	TGGGAGGCTGAGGCG[A/G]GTGGATCACCCAAGG	80176
rs769341435	in-del	-/C			intron-variant	SPSB1	GRCh38.p7	1:9330704	GCATGTTCTTCTGAA[-/C]TTTTTTTTTTTTAAT	80176
rs769373732	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9312469	CCTATTGTAAATGTA[C/T]ACATTGATGATTATT	80176
rs769406033	snp	A/G	3.53457e-05	0.00420376	missense	SPSB1	GRCh38.p7	1:9356175	AAGTCGGGTATACCC[A/G]TGGGCTGCACGTGTG	80176
rs769411013	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9343230	CCCAAAACAGTTTCA[A/T]CACCCCTAAAAGAAA	80176
rs769413536	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9352400	GCAGGGCCCTGTCTA[A/C]GCTCTGGCTGGCGGA	80176
rs769440436	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9329477	GAAGATGGGCATGGC[C/T]ACCCATCAGAAGTTA	80176
rs769455899	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9320742	GCTCTGGCTGGCCAC[A/G]ACCTTCCTTTTGAAG	80176
rs769513160	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9353627	CCCTGAGATCAGAAC[C/T]CTCTGTCTATGGCTG	80176
rs769534396	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9338325	ACCCTGTCCCCAGGG[A/T]GGAGGTTCGTGACTG	80176
rs769688999	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9328371	TCAGCAGAACCTTGC[A/G]TTTCTGTCCTGCGGG	80176
rs769709084	in-del	-/AATAGC			intron-variant	SPSB1	GRCh38.p7	1:9330470	ATTCTGTCTCAAAAT[-/AATAGC]AATAACAATAATAAT	80176
rs769715973	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9344253	GAATGCAGGCTGCCC[C/T]GTGGAGTTTCTGATT	80176
rs769746017	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9321212	CAGAGGCGTCTCAGG[C/T]GGTGGGCCTTAAACA	80176
rs769759621	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9298932	CTGCCTGGGAAAATA[C/G]TACATCAAAAGCAAC	80176
rs769771908	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9337820	TGTCTCTCCTGGGAC[A/G]CCCCATGAAGCCAGG	80176
rs769814640	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9346405	GACAGACCCACCTCT[C/G]TGCATCCTTTACCTG	80176
rs769821426	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9331728	AGATCCCACCAGCCA[C/T]GTTGGTACTTGCTCT	80176
rs769849881	snp	A/G			missense	SPSB1	GRCh38.p7	1:9356565	GTGAGATCCGAATGC[A/G]CTACTTGAACGGACT	80176
rs769868075	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9328858	GCGTGGCTGGGCGTT[C/T]AGCAATATCCCTGGC	80176
rs769871001	snp	A/G	1.65504e-05	0.00287662	missense	SPSB1	GRCh38.p7	1:9356297	ACCCTCGTGGGGAAT[A/G]ACCACGAGTCCTGGG	80176
rs769907012	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9340697	GCCTTCCCTGCCACC[A/G]AGGGGCGTGGGATGC	80176
rs770051537	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9307759	ATTTGTATCTTTTCC[C/T]GTTGATCTATTAAAA	80176
rs770055673	snp	A/C	3.22471e-05	0.00401529	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9367593	TTCGCCATCATACCG[A/C]CAGCGCGACAGCCAC	80176
rs770062807	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9365879	CCATCTGCAGAACAG[C/T]GTGGGCGGCCCCACG	80176
rs770065079	snp	C/G	1.64781e-05	0.00287033	missense	SPSB1	GRCh38.p7	1:9356432	TCCTTCCTGGTAGCC[C/G]TGGACATGGACGACG	80176
rs770088641	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9330835	AGTTTGAGGAACCAC[C/T]CTACTGTGTCCAGCG	80176
rs770089972	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9349890	AGCTCCCTGTCACCC[A/G]TGAGGAGGACGGTCC	80176
rs770144020	snp	C/T	0.00020858	0.0102101	missense	SPSB1	GRCh38.p7	1:9367529	TGGGGGAGATCCACA[C/T]GCTGCCGCTGCCGGC	80176
rs770247548	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9304289	TCAGACTTGGCTGAG[C/G]CACACTCCTGGCTCC	80176
rs770284330	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9360972	CACGTCACCCCTACC[A/G]ATGCTGGGGTGCCCA	80176
rs770304339	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9359501	GAGGTCAGTAGTTGG[A/T]GACCAGCCTGGCCAA	80176
rs770336631	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9293680	GGAGGGTTGTCAGGA[A/T]ATCGATTAAATCAGA	80176
rs770454759	snp	A/G	5.06975e-05	0.0050345	synonymous-codon	SPSB1	GRCh38.p7	1:9355945	CATGAGGGACCCCAC[A/G]TACAGGCCCCTGAAG	80176
rs770455045	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9325864	CCTGGGGCCTCAGGC[C/T]CGGTGTGCCCAGAGC	80176
rs770517892	snp	C/G/T			intron-variant	SPSB1	GRCh38.p7	1:9349322	CTCCCGCCACGTGCT[C/G/T]GACTTTGATATTGGT	80176
rs770525035	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9365251	CTCCTGGGCCCAACC[A/G]ATCCTCTCGCCTCAG	80176
rs770527113	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9304405	TCTGTCTCTCCCTCT[C/T]GATCCTATGGGTTTT	80176
rs770530546	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9335774	GATCGTGCCACTGCA[C/T]TCCAGCCTGGACGAC	80176
rs770615290	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9313273	GACGTGGTGCCGGGC[A/G]CCTATAATCCCAGCT	80176
rs770632012	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9321542	TTCAGCTCAGAACGG[A/G]GAAGAGGGTGTTTGA	80176
rs770642781	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9307087	CACGTGCCACCACGC[C/G]TGGCTAATTTTTGTA	80176
rs770655951	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9354758	GTGAGCCGAGATCAC[A/G]CCACTGCACTCCAGC	80176
rs770688591	snp	C/T	3.54039e-05	0.00420722	synonymous-codon	SPSB1	GRCh38.p7	1:9356575	AATGCGCTACTTGAA[C/T]GGACTCGATCGTAAG	80176
rs770704888	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9312582	GACTGGGGGAGGGCC[A/G]CATTCTCCCAAGTTT	80176
rs770733969	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9330597	ATCCCTAACTTCACC[C/T]GACACGTTTGGGGGA	80176
rs770738877	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9359068	TCGGGAACCGCATCT[A/G]TGAGCTGGAATCTAG	80176
rs770780832	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9354001	TGAGATAAGGGGGTC[A/G]GGGCACCAAGTGTTC	80176
rs770799621	in-del	-/A			intron-variant	SPSB1	GRCh38.p7	1:9298250	TATAAGCAGAAACTT[-/A]ACAGGTCAAATGAAA	80176
rs770835802	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9352584	GCTGATCTCCGGTCT[C/T]GCTGAGACAGGCGTT	80176
rs770847406	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9300667	AAGTGGGTGTTATCT[A/G]TGATCTGACCGACCA	80176
rs770898887	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9301561	AGTGCGCACAGGACA[C/T]GGATAGACCTCCCGA	80176
rs770907896	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9315980	CAGTTCTGCAGCCAG[C/T]GGGGCCTCTTGGCAG	80176
rs771005943	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9301574	CACGGATAGACCTCC[C/T]GAGTGCGCACAGGAC	80176
rs771040577	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9367163	CATCTGTAAAATGGG[A/G]ATGAAGGTAATGGTG	80176
rs771170841	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9345658	CAGGCCATGGCTCCA[C/T]TGATTCGAGCCCTCT	80176
rs771173052	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9332480	GGGGCCATTTGAGTC[A/T]ACAAGGGATGTATGA	80176
rs771205102	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9357719	GTGGCCTTTCTCAGA[C/G]TGTGAATGCAGCCCA	80176
rs771213035	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9322390	GCTCCAAAGTCCGTG[A/C]CTCGCTCTCATTTTT	80176
rs771261156	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9341403	TTGGGTGTTGCCTGC[C/T]TCCCCCCACTAGACT	80176
rs771323541	in-del	-/A			intron-variant	SPSB1	GRCh38.p7	1:9310696	GTTAGACCTTGTCTT[-/A]AAAAAAAAAAAAGAG	80176
rs771365894	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9349999	ACACACGTGTACCTA[C/T]ATGCACACACAGCAC	80176
rs771430034	snp	C/T	3.32651e-05	0.00407817	missense	SPSB1	GRCh38.p7	1:9367454	TCTCCCCAGCCGAGC[C/T]GCTGCCGCTCATGGA	80176
rs771460360	snp	C/T			synonymous-codon	SPSB1	GRCh38.p7	1:9356464	GACTCTGAGCTTCAT[C/T]GTGGATGGACAGTAC	80176
rs771536075	in-del	-/TGGGTGGATGGATGGG			intron-variant	SPSB1	GRCh38.p7	1:9357146	GAGTGGATGGATGGA[-/TGGGTGGATGGATGGG]TGGATGGATGGGTGG	80176
rs771560648	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9340626	CTGTGGGGCTGGGGA[C/G]GGTCCCCGCAGCACC	80176
rs771562509	snp	C/T	6.63504e-05	0.00575941	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9367619	GCCACCTGGTGCCAA[C/T]TCACTGAGCCGCCTG	80176
rs771563134	in-del	-/G			intron-variant	SPSB1	GRCh38.p7	1:9306380	GTCCAGCCTGGAGGA[-/G]GTGGAAGATGGATGG	80176
rs771583370	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9318142	GGCCCAGTGAGGGTG[A/G]GGCCCTGGGGTCTGG	80176
rs771626598	snp	A/G	1.68196e-05	0.00289992	synonymous-codon	SPSB1	GRCh38.p7	1:9367518	GAGGGAGCGCCTGGG[A/G]GAGATCCACACGCTG	80176
rs771631342	in-del	-/GGATGGGT			intron-variant	SPSB1	GRCh38.p7	1:9329280	GAAAGGTGAGATCCC[-/GGATGGGT]GGATGGGTGGACAGG	80176
rs771657963	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9326775	CCCGCTGCTTCTGAG[A/G]GGCCTTCCTCATTCC	80176
rs771659792	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9348013	GCAGTGGTGCGATCT[C/T]GGCTCACTGCAACCT	80176
rs771660261	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9305427	GCTCCAGGAGGGCAG[A/G]ACCCGGCCGGCCACA	80176
rs771661500	snp	A/G			upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291568	TGAGCCATCATGCCC[A/G]GCCAATTATTATTAT	80176
rs771680830	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9350129	ACACCCCTACCACCC[A/G]CACAGGTACACACAC	80176
rs771712799	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9349657	CTCGTGCCACACACA[A/G]TCCGCCACCAGCATC	80176
rs771716001	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9306183	TGAGGGCACCTCAGG[C/T]GATTGCCTGTTGCCA	80176
rs771727476	in-del	CGG/TTGGGCCAGGATGGAAGCC			intron-variant	SPSB1	GRCh38.p7	1:9359829	AGAGGTGATGGGAGC[CGG/TTGGGCCAGGATGGAAGCC]GGGGGGGTGGGTGGC	80176
rs771743590	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9337159	GGGGTGCTTTCTGGT[C/T]GTTTCCATCTGGTTG	80176
rs771745720	snp	A/G	1.66632e-05	0.0028864	missense	SPSB1	GRCh38.p7	1:9356279	CACTCTGTCGGGTAC[A/G]CAACCCTCGTGGGGA	80176
rs771758600	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9330722	TTTTTTTTTTAATCG[G/T]GGTAAAACATACAAA	80176
rs771830575	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9361023	CAAGTCCCCCGTCCC[A/G]GGAGAGTTGGCTTTG	80176
rs771833499	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9336077	TCTGAGGCTCTCTGC[A/G]GGCTTCCAGGGTAGG	80176
rs771833593	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9345315	TTTCTTGGAGATGGC[C/T]GTGGGGCTGCTTTTG	80176
rs771936778	snp	C/T	1.64762e-05	0.00287016	synonymous-codon	SPSB1	GRCh38.p7	1:9356410	TGAGACATTCATTGT[C/T]CCTGACTCCTTCCTG	80176
rs771977393	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9313362	CCAAGATTGCACCAC[G/T]GCACTCCAGCCTGGG	80176
rs772005360	in-del	-/GAGAGTGT			intron-variant	SPSB1	GRCh38.p7	1:9309298	TGAGAGAGAGAGAGA[-/GAGAGTGT]GTGTGTGTGTGTGTG	80176
rs772103176	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9363222	GTTTCCTCCTGCAAG[A/G]TCAAGGAGGCGTGAC	80176
rs772159796	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9321601	ATGCATAGGCAGCTC[A/G]CTAATGCTGTGTTTC	80176
rs772206113	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9358471	GTGTCTGTCTCCCTA[C/G]GTGTCAGAAATGAGT	80176
rs772258094	snp	C/G	3.33161e-05	0.00408129	intron-variant	SPSB1	GRCh38.p7	1:9367444	AGTTTCTCTGTCTCC[C/G]CAGCCGAGCCGCTGC	80176
rs772297436	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9326919	TTTTTAGGTGGAGGC[A/G]GGGACCCTAACCCCT	80176
rs772324138	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9345091	AGGCAGCCCTGAACT[C/T]TGGAGTCCCACAGGA	80176
rs772345647	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9347783	GCCCTGGAAGGGCTG[C/T]TGCTGGGTGATTGCT	80176
rs772365651	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9316166	GGCTGGCAGGGGGTG[G/T]GGACCTGGGTGAAGA	80176
rs772399009	snp	A/G	4.96356e-05	0.0049815	missense	SPSB1	GRCh38.p7	1:9356064	TGCATTCATGGAACA[A/G]CAACGACCGATCGCT	80176
rs772416772	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9357762	CCGTGCTGGTGTGGG[A/T]GGTGAAGGCTCCATG	80176
rs772436653	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9346954	GTCTTGGGATAGATC[A/G]CTGTAGAAATAATGT	80176
rs772451725	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9333519	TATTTTTAGTAGAGA[C/T]GGGGTTTCGCCATGT	80176
rs772498697	in-del	-/T			intron-variant	SPSB1	GRCh38.p7	1:9333331	TCTTGTCAGCTTCTT[-/T]TTTTTTTTTTTTTTT	80176
rs772545430	snp	G/T	1.66167e-05	0.00288237	synonymous-codon	SPSB1	GRCh38.p7	1:9367488	GTGCCGTCGCTCGGT[G/T]CGCCTGGCCCTGGGG	80176
rs772577520	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9301861	TGGTGGAAGGCACAT[G/T]GGACCACTTCTGTTT	80176
rs772605700	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9347621	TTGCTTTACAAATGC[A/G]ACAGCATCGTGTTAC	80176
rs772656236	in-del	-/T			intron-variant	SPSB1	GRCh38.p7	1:9330706	ATGTTCTTCTGAACT[-/T]TTTTTTTTTTAATCG	80176
rs772656948	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9354531	ATCTTCTGCTGCCTT[A/C]TCCTTCTCCTTGAAT	80176
rs772666835	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9302910	GACCCGCTAGCGAAA[C/T]TGTTGCTTCCTGTTC	80176
rs772693646	in-del	-/CTC/CTCG			intron-variant	SPSB1	GRCh38.p7	1:9299489	TCTCTCTCTCTCTCT[-/CTC/CTCG]TTTTTTGAGATGGAT	80176
rs772773642	snp	A/G	1.83122e-05	0.00302585	intron-variant	SPSB1	GRCh38.p7	1:9356610	TCCTCTGCTGTCAGA[A/G]GCAATGCCCTCCCTC	80176
rs772779962	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9325866	TGGGGCCTCAGGCCC[A/G]GTGTGCCCAGAGCCA	80176
rs772783309	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9344500	TGGCATTCCCTGGCT[A/G]AGCGCTCTCCTGCAC	80176
rs772792927	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9304952	GGCATGAGCCACAGC[A/G]CTCACCCTCTGCTGC	80176
rs772848690	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9299381	CGGTGGCTCACTCCT[A/G]TAATCCTAGCACTTC	80176
rs772867459	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9334912	AATATTTCATCGTGG[C/G]GATGGGCCCCATTTT	80176
rs772903540	in-del	-/TTT			intron-variant	SPSB1	GRCh38.p7	1:9317838	TGGCGAGGGAACCAA[-/TTT]TTTTTTTTTTTTTTT	80176
rs772909029	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9306275	GCGTCCTGCAGCAGT[C/T]GGCTTTTCTGCTCTG	80176
rs772934500	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9302199	TGCCAGTGGGTGCCT[A/G]TGGGTGCCAGTTGGT	80176
rs772953531	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9311473	ACCCAGCACCAACAA[A/G]TATTCGCTGGTCTCT	80176
rs772961276	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9365189	CAAGGTCTCTGTTAC[A/G]CAGGCTGGAATACAG	80176
rs772979732	snp	A/G			utr-variant-3-prime	SPSB1	GRCh38.p7	1:9367962	GGTGGTGGGGGTGGC[A/G]GGTGGTACCACAGCT	80176
rs773005646	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9351543	GAGCTACTGTCTCGG[C/T]GCATGAGCTTGGAAG	80176
rs773015596	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9328393	TCCTGCGGGACTTCT[C/T]AGAGCCTTTAAGATG	80176
rs773056435	snp	C/T	8.30255e-05	0.0064425	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9367623	CCTGGTGCCAACTCA[C/T]TGAGCCGCCTGCCGC	80176
rs773078171	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9363169	TGGTCTCTGCCCAGC[C/T]TTTGGAAAGCAGTTA	80176
rs773094043	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9352500	TCTGTGGCTGCTTTT[C/G]TGCGACAACAGCAGA	80176
rs773112032	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9345607	AGCTGCGATATATTG[C/T]AATTTTCAGTCTGTT	80176
rs773171397	snp	C/T			utr-variant-3-prime	SPSB1	GRCh38.p7	1:9368074	ATGGCAGATAAAGCT[C/T]AGGACGTCAAAAACT	80176
rs773217808	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9328873	TAGCAATATCCCTGG[C/T]CCCCACCCACCAGAC	80176
rs773289647	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9294768	ATTTCTCATCGTGGG[G/T]TGTGAGGAGAACAGC	80176
rs773335378	snp	C/G	3.36859e-05	0.00410388	missense	SPSB1	GRCh38.p7	1:9356098	TGTCTTTGTGAAGGA[C/G]GACGACAAGCTCATC	80176
rs773387725	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9314919	AGAACAGCATGTCCT[G/T]CACACAGGAGTGGCC	80176
rs773388707	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9322314	GGGAAACTGAGGTTC[A/G]GAAAGTCTCTCAGGT	80176
rs773390159	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9330849	CCCTACTGTGTCCAG[C/T]GGCTGTGCCATTTTG	80176
rs773402611	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9308641	GTGCCATGAGCCAGG[C/T]GCTATGCTTGCCACT	80176
rs773420219	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9339313	CTGGCCAGCCACATG[C/T]GGGTGGTCTCGGGTG	80176
rs773473294	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9340727	CACCCGTCCCCTGCT[C/T]GCCCCTCTGCCTGCA	80176
rs773478634	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9331735	ACCAGCCACGTTGGT[A/G]CTTGCTCTCCGCTTC	80176
rs773486392	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9318070	TTCCGGGCAGGTTGG[A/G]GAAACGCAGCGATTG	80176
rs773503679	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9340316	ACTGGTGTTTGGGGA[C/G]TGGCCGGAGCCCCGC	80176
rs773534385	in-del	-/TT			intron-variant	SPSB1	GRCh38.p7	1:9306915	TCTTTTTTCTTTTAC[-/TT]TTCTTCTTTTCTTCT	80176
rs773551521	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9355420	GGCACCATGGCCTTC[C/T]GCCCTGTGGAACCCT	80176
rs773591274	in-del	-/TA			intron-variant	SPSB1	GRCh38.p7	1:9354149	CCTGGCCCTGGCTGG[-/TA]CCCCATACTGAAGGG	80176
rs773595647	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9339430	GGCGAGTCTGGAGGC[A/G]ACGGAGAGGTGCTCT	80176
rs773681514	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9338753	CCCCCATATGACTTC[A/G]TGGCTGTGAAACGTG	80176
rs773686261	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9293681	GAGGGTTGTCAGGAA[A/T]TCGATTAAATCAGAA	80176
rs773733365	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9364722	ATACAGAACATTTCA[A/G]TTCCTTGTCAGGAGC	80176
rs773769664	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9348235	CAGGCGTGAGCCACC[G/T]CGGCAACTTTTTTTA	80176
rs773785036	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9326725	GCCTGATCATCAGCC[G/T]TCTTCCCTCCCACTG	80176
rs773811972	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9350234	GCACCAGACATTGGA[A/C]CCCTGCGTGTGACAG	80176
rs773812173	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9359538	GAAACCCCATTTCTA[C/T]TAAAAATGCAAAAAT	80176
rs773860481	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9346770	TTTCTGATGGGGCCA[C/T]CTCACCTGGCCTTTG	80176
rs773868793	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9335800	ACGACAGGGCAGGAC[C/T]CTGTCTGTGAAAAAA	80176
rs773908512	snp	A/G	1.75277e-05	0.00296033	synonymous-codon	SPSB1	GRCh38.p7	1:9367539	CCACACGCTGCCGCT[A/G]CCGGCTTCCCTCAAG	80176
rs773941473	in-del	-/GT			intron-variant	SPSB1	GRCh38.p7	1:9309299	AGAGAGAGAGAGAGA[-/GT]GAGTGTGTGTGTGTG	80176
rs773961593	snp	C/T	8.14299e-05	0.00638031	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9367602	ATACCGCCAGCGCGA[C/T]AGCCACCTGGTGCCA	80176
rs774046073	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9326019	TCCTGGCCAGGAGGA[A/G]TGTGGGCTCCATGAG	80176
rs774050724	snp	C/G/T			intron-variant	SPSB1	GRCh38.p7	1:9312644	CAGCACGGAGTTTTG[C/G/T]TGGACGAGCAGCTCA	80176
rs774132359	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9342573	ACGTCCCTCTCCCGC[A/C]TCATCCTGCCTTGTT	80176
rs774136012	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9335078	GTGGATTTTCTAGGT[A/C]ATATGGTAATTCTAT	80176
rs774139927	snp	A/C/T	3.53408e-05	0.0042035	synonymous-codon	SPSB1	GRCh38.p7	1:9356197	GCACGTGTGGCAGAT[A/C/T]ACGTGGGCCATGAGA	80176
rs774155177	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9340903	ACCTGGCTGCGGTGC[A/G]GGGAGGCAGAGTGGG	80176
rs774236625	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9337891	CCCAAGAGCACCTTT[A/T]GGGGCGGGAGGGGTA	80176
rs774260726	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9301564	GCGCACAGGACACGG[A/G]TAGACCTCCCGAGTG	80176
rs774309877	in-del	-/T			intron-variant	SPSB1	GRCh38.p7	1:9311834	TGCATCCCTGGGGGG[-/T]ATGAATTTTCTTGGT	80176
rs774333493	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9357408	TCTTTGTTTCTCTGG[A/G]TGACCTGCCTCCAGG	80176
rs774399810	in-del	-/GTGTGTGTGTGAGAGTGTGA			intron-variant	SPSB1	GRCh38.p7	1:9295198	GTAGATGGAGTGTGT[-/GTGTGTGTGTGAGAGTGTGA]GTGTGTGTGTGTGTG	80176
rs774429918	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9327768	ATATGGTGTCTGCCG[C/T]AACTACTCGACTCTG	80176
rs774516993	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9337402	GGCAGGCACCTCACA[C/T]CTGGCCAGCCACCTG	80176
rs774540909	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9323165	CCATGTTGGAGGGGG[C/G]TATCCATGGGGCCTC	80176
rs774554219	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9300676	TTATCTATGATCTGA[C/T]CGACCAAACCAGACA	80176
rs774587594	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9350507	TGCCTGGACTATGAC[A/G]CCTCTGTCCTGCTTG	80176
rs774606398	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9325088	CGCTGGAAGCTGGGA[C/T]TCCAGAGCTCAGCAC	80176
rs774786838	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9361475	CCAGCAGTTTGCCTG[C/T]GTGTGTGCCTTCCCG	80176
rs774806925	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9340435	GGCGTTGTGTTATGA[A/C]AACGTGGGTCCCAGA	80176
rs774807703	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9331815	GGAGGGTGCAACGTG[C/T]GATCTCATTACTGCT	80176
rs774856628	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9365318	GATGAGGTCTCCCTA[C/T]GTTGCTCAGGCTGGT	80176
rs774878493	in-del	-/TGT			intron-variant	SPSB1	GRCh38.p7	1:9294043	CTGTGTGTGTGTGTG[-/TGT]GTCTGAGTGCGTCTT	80176
rs774952366	snp	C/T	1.65773e-05	0.00287895	missense	SPSB1	GRCh38.p7	1:9356495	ATGGGAGTGGCTTTT[C/T]GGGGACTCAAGGGCA	80176
rs775007521	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9341505	TCCAGCCCTGAGGCA[C/T]ATTATTTGGACTTGG	80176
rs775117337	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9330725	TTTTTTTAATCGTGG[A/T]AAAACATACAAAAAC	80176
rs775143583	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9351215	AGTTACTATCTGGCC[C/T]CTGATGGAAGAAGTT	80176
rs775152382	snp	C/T			upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291668	TAAGTGATCTGCCTG[C/T]CTCAGCCACCCAAAG	80176
rs775168600	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9332428	GGGTGAACTAGAGGT[G/T]GATGATAGAAATTGG	80176
rs775173590	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9325752	GAGCATGGCACGGGG[G/T]CAAAGGACGTTTGCC	80176
rs775203239	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9337160	GGGTGCTTTCTGGTC[A/G]TTTCCATCTGGTTGT	80176
rs775212777	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9304566	GGCATCTCCAAGGTG[C/G]CATGGGTAAGCTTCG	80176
rs775287638	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9336168	TGAAATGTTATTTCT[C/T]GGGTTGTTAACTCAC	80176
rs775323857	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9361061	ATACAACTAAAGAAG[C/G]GGGGTGTCCTGGTGA	80176
rs775332970	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9305437	GGCAGGACCCGGCCG[G/T]CCACATGGCTGTTGT	80176
rs775377603	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9344233	GTTCCCTGGAGGGCT[C/T]ATTAGAATGCAGGCT	80176
rs775408653	in-del	-/CC	3.40846e-05	0.00412809	intron-variant	SPSB1	GRCh38.p7	1:9367442	GCAGTTTCTCTGTCT[-/CC]CCAGCCGAGCCGCTG	80176
rs775422922	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9314670	TCTTCTTACATCGTC[G/T]TGTTTTTCTCCGGGA	80176
rs775443412	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9301884	TTCTGTTTTGGAAGG[A/G]GCAGCGTTTTGTCCT	80176
rs775448548	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9360112	TGTCTGCACATAGGC[A/G]ACTTCAGAGCTGCCA	80176
rs775536560	snp	C/T	1.66322e-05	0.00288371	synonymous-codon	SPSB1	GRCh38.p7	1:9356086	CCGATCGCTCAATGT[C/T]TTTGTGAAGGAGGAC	80176
rs775585329	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9306692	GCCACAAAAGAGGAG[C/T]GAGGAAGAAATGAGC	80176
rs775591521	snp	C/T	1.76836e-05	0.00297347	synonymous-codon	SPSB1	GRCh38.p7	1:9356185	TACCCGTGGGCTGCA[C/T]GTGTGGCAGATCACG	80176
rs775597030	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9353211	CGGCCCCTCGAGAGC[C/T]GCCTCGGCCCTCCCA	80176
rs775600590	snp	C/T	3.3089e-05	0.00406736	synonymous-codon	SPSB1	GRCh38.p7	1:9356302	CGTGGGGAATAACCA[C/T]GAGTCCTGGGGCTGG	80176
rs775627022	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9310055	TAAAGCTCTCCTCAG[A/G]TGGGGGATGGTGAGG	80176
rs775632214	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9346978	ATAATGTCCCTCTTC[A/G]GGATGGCCCCAAAGC	80176
rs775647147	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9329840	GGAGGTAGAAGAGAG[C/T]GTTCTGTGGGTAACG	80176
rs775662267	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9363350	TTCACTGCCACTTCT[C/G]TAGCCCGTCTTGGTG	80176
rs775731000	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9328530	CTGATTTCTTTCAAT[A/G]CTTCGTTTTATAAAC	80176
rs775749663	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9311111	CCTGAAAGCCAAGTC[C/T]TTACCCCCACGCCAC	80176
rs775794386	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9363311	CTGGTCCTATTTTCA[A/G]CTCATAACACATCAC	80176
rs775794778	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9316217	GCCGGCCTCCCTGAC[C/T]CTGGGGCTCCGGCAC	80176
rs775794829	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9324491	CCCAGCCTCTGGAGG[C/G]TCGGCTCGGAGGGCT	80176
rs775822746	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9337929	AGAGTGACCTGGTGG[C/T]TCTTCCGGTGAGGAA	80176
rs775901936	in-del	-/T			intron-variant	SPSB1	GRCh38.p7	1:9331290	TGTCATAAATACCCG[-/T]TATGGATCTCCTTCT	80176
rs775934017	in-del	-/TT			intron-variant	SPSB1	GRCh38.p7	1:9333330	TTCTTGTCAGCTTCT[-/TT]TTTTTTTTTTTTTTT	80176
rs775954617	in-del	-/TTCTTC			intron-variant	SPSB1	GRCh38.p7	1:9306917	TTTTTTCTTTTACTT[-/TTCTTC]TTTTCTTCTTTTTTT	80176
rs776030845	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9332717	CACAAAACTAGGAGC[A/G]TTTCAGGTCAAGGGC	80176
rs776133652	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9337703	GACTCCCTGGCCACC[A/G]GGGCCCTGAGCCAAT	80176
rs776146642	snp	A/G	0.000199193	0.00997782	synonymous-codon	SPSB1	GRCh38.p7	1:9356077	CAACAACGACCGATC[A/G]CTCAATGTCTTTGTG	80176
rs776189207	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9320026	GGGAGTCTGTGCTTC[A/G]AGCCCCCTGGGCCAG	80176
rs776200990	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9302113	GAGCCCACTGGTTTC[A/G]CCTATCATGCTAAGT	80176
rs776217613	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9333745	ATTTTTTTATTCCAA[C/T]GGAAAGGAAACGAGG	80176
rs776319341	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9311213	CAGTATTCCCTGAAT[G/T]CCCGCTCTGTCCTGG	80176
rs776320885	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9318537	AGTTTGGAATCTGGC[C/T]TCCAACCTGGATCCT	80176
rs776361185	snp	A/C			upstream-variant-2KB	SPSB1	GRCh38.p7	1:9291809	AACATTCCTAAACCG[A/C]TGGCACCTGGAAAGT	80176
rs776386365	in-del	-/C			intron-variant	SPSB1	GRCh38.p7	1:9345994	CCAGCACGGAGCATG[-/C]CCCGAGCCCTTCCAC	80176
rs776391642	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9351450	CTCTGGAACACTGTC[C/T]CCACTGAGTTTTAGG	80176
rs776430995	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9337235	TCTGAGCCTCTAACC[A/C]CCGGGATTAGCTCCA	80176
rs776459202	snp	A/T	1.68505e-05	0.00290258	missense	SPSB1	GRCh38.p7	1:9355947	TGAGGGACCCCACGT[A/T]CAGGCCCCTGAAGCA	80176
rs776488424	in-del	-/C			intron-variant	SPSB1	GRCh38.p7	1:9359106	CTCAGAGCATCACAG[-/C]CGGGCGCTATTAGTC	80176
rs776516759	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9362336	CTGATCACCTAGGTG[A/G]ATCTCAGGCGTCCTT	80176
rs776568463	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9340589	GCTGTGGAAACTCCA[C/T]GCCTGGCGGGAAGAT	80176
rs776604287	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9365167	TGGCCTGTTTTCATT[G/T]TTGAGACAAGGTCTC	80176
rs776670032	in-del	-/GG			intron-variant	SPSB1	GRCh38.p7	1:9319742	GTCCGCTGTAGTGAA[-/GG]GAGGGTACTACAGGG	80176
rs776760806	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9297829	TGGAATGCTGGAGTG[C/G]ATTTGTCTCTTAAAA	80176
rs776803132	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9354197	GGTCCCTGGATTTCC[A/G]TGTGTCTGGGAGCCT	80176
rs776804247	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9338643	TGGAAAAGGGTCTGG[C/G]AAGGGAATCGTGCTG	80176
rs776808212	snp	A/G	4.98931e-05	0.00499441	synonymous-codon	SPSB1	GRCh38.p7	1:9367455	CTCCCCAGCCGAGCC[A/G]CTGCCGCTCATGGAT	80176
rs776895972	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9354817	AAAAAAAAAAGAATT[C/T]TTCCTGGGCTACCAG	80176
rs776901346	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9330795	AGTAGCGTTGAGTAC[A/G]TTACCGGATCGTACG	80176
rs776912087	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9339377	ACTCACCGCCAGGCC[A/G]GGTTCTGGCAGGACC	80176
rs776931132	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9307167	TCCTGACCTCAGGTG[A/C]TCTGCCCGCTTTGGC	80176
rs776988563	snp	A/C/T			intron-variant	SPSB1	GRCh38.p7	1:9348092	TGGGATTACAGGTGC[A/C/T]CACCACCACGCCCAG	80176
rs776989322	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9330180	TGTACACATAAAGAT[A/G]TACCAGGCTGGGCAC	80176
rs777094143	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9316749	CAGGGGAGACCGCCC[C/T]GGAAGCGGCATTGGG	80176
rs777246199	in-del	-/GC			intron-variant	SPSB1	GRCh38.p7	1:9343361	AATCGTACAATGTGT[-/GC]GACCTTTTATATCTG	80176
rs777335780	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9313226	ACATGATGAAACCCT[G/T]TCTCTACTAAAAAAA	80176
rs777342432	snp	C/T	1.65474e-05	0.00287636	synonymous-codon	SPSB1	GRCh38.p7	1:9356065	GCATTCATGGAACAA[C/T]AACGACCGATCGCTC	80176
rs777351848	in-del	-/CGCGCCCCGCGCCC			upstream-variant-2KB	SPSB1	GRCh38.p7	1:9292725	CCAGCGCCGGGCTGA[-/CGCGCCCCGCGCCC]CGCGCCCCGCGCCCC	80176
rs777352214	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9335661	AAAAACTAGCTGAGC[A/G]TGGTGGTGCATTCCT	80176
rs777363519	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9343940	AGAGGCGCCTGCCAC[C/T]ACGCCTGGCTAATTT	80176
rs777389305	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9330580	GTGATCTGGACACAC[A/G]TATCCCTAACTTCAC	80176
rs777413243	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9322107	TGAATGGCTCTTTAT[G/T]AACGACCCACATTCC	80176
rs777417450	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9338769	TGGCTGTGAAACGTG[A/G]GTGGCGTGGGCCACG	80176
rs777451849	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9364976	CCTGCCTTAGCCTCC[C/T]GAGTAGCCGGGACTA	80176
rs777482268	snp	C/T	1.64762e-05	0.00287016	synonymous-codon	SPSB1	GRCh38.p7	1:9356419	CATTGTCCCTGACTC[C/T]TTCCTGGTAGCCCTG	80176
rs777497794	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9331393	TGGAGTACAGTGGTA[C/T]GATCTTGGCTCACTG	80176
rs777590297	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9298564	CTTCCCCAAAGGGAC[C/T]TGTGACCTTTTACCA	80176
rs777678842	snp	C/T	3.48967e-05	0.00417698	synonymous-codon	SPSB1	GRCh38.p7	1:9356570	ATCCGAATGCGCTAC[C/T]TGAACGGACTCGATC	80176
rs777679509	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9307507	TGCATGGCCTTCTGC[G/T]TCTGACTTCTGGCTA	80176
rs777761539	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9338446	ACTTGTGGGGGTCAG[C/T]GTACCTAAGGCCACC	80176
rs777773879	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9316971	GAGATCCCAGGCCCC[A/G]TAGCAGGGCCAGGCC	80176
rs777814521	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9349306	GTGCATGAGACAGAC[A/G]CTCCCGCCACGTGCT	80176
rs777869587	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9333129	AATGGCCAGAAACAT[A/G]GAACCCACCTTCTTC	80176
rs777877192	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9342169	GATGGTGGAGTTCTC[A/G]GCCGACTTCCCATGT	80176
rs777889715	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9300618	TTTGACCATCAGCCA[C/T]GAAGTTGCCATGTGA	80176
rs777935679	snp	C/G	5.02753e-05	0.00501349	missense	SPSB1	GRCh38.p7	1:9367513	CTGGGGAGGGAGCGC[C/G]TGGGGGAGATCCACA	80176
rs777967501	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9359057	GGAATCAGGATTCGG[A/G]AACCGCATCTGTGAG	80176
rs777976202	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9310610	TGAGGCAGGAGGATC[A/C]CTTGAGTTTGGGAGG	80176
rs778084044	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9316827	CTGGCTTTCCACCTC[A/G]GTTCTCCCTGCTCCT	80176
rs778131096	snp	C/T	2.32075e-05	0.00340635	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9367576	CTCCTCTACCAGTGA[C/T]GTTCGCCATCATACC	80176
rs778146891	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9318842	TGAGCTGGTGATTGT[A/C]ACACAGGGTGACAAA	80176
rs778209844	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9326623	CTGGGGGACCAGAGG[C/T]CTTGCTGAGGCTCCT	80176
rs778248519	snp	C/T	3.43589e-05	0.00414467	stop-gained	SPSB1	GRCh38.p7	1:9356558	GGCCACTGTGAGATC[C/T]GAATGCGCTACTTGA	80176
rs778280838	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9305220	CCGCCTCGGCTGGCC[C/T]GTTCCTACCGGCTGG	80176
rs778320765	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9327151	AGCGCTTCCGGGGGT[C/T]CCAGGATGGCCCTCT	80176
rs778360607	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9306101	GCCATGCTCCTGCAG[C/T]GGGAGGAACCGAGAC	80176
rs778409049	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9336684	GCTAGTGAGGACGCA[A/G]CTCCTGGCCGGCTCG	80176
rs778521609	snp	C/T			utr-variant-3-prime	SPSB1	GRCh38.p7	1:9367707	TCCCTGGTCTTCCCT[C/T]ATCCTCCGTGGCTGC	80176
rs778524564	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9322157	GTCGAGGCTGGCTCC[A/G]TCTTTGCCTTGGACT	80176
rs778545141	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9315667	GATGCAGCCTGGTTT[C/T]GACCCTCTACTAGGG	80176
rs778633006	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9322831	TGACGTGTAGGGAAG[C/T]GCTGCGTTAGGTCAC	80176
rs778654267	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9322099	AAGGGGCTTGAATGG[C/T]TCTTTATTAACGACC	80176
rs778778928	in-del	-/GT			intron-variant	SPSB1	GRCh38.p7	1:9324507	TCGGCTCGGAGGGCT[-/GT]GGGCCCGGGACTCGG	80176
rs778898733	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9365109	TAATGCGCCGGCCTC[A/G]GCCTCCCGAAGTGCT	80176
rs778918593	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9325496	TGGTGTGGGCGACCC[G/T]AGGCCCTGCTTCTAT	80176
rs778962154	snp	A/G	1.6477e-05	0.00287024	missense	SPSB1	GRCh38.p7	1:9356387	TACCCAGCCTTTCTG[A/G]AACCAGATGAGACAT	80176
rs778964316	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9334585	CTTCATATTGTTGTA[C/T]AACCATCACCGTTGT	80176
rs778985164	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9330632	TTTGGGTTTGCCTGT[C/T]CTCTTCCTTTCCTCC	80176
rs778990450	snp	C/T			utr-variant-3-prime	SPSB1	GRCh38.p7	1:9368350	GCACACGTGCCCAGG[C/T]ACAAGTATGTCTCTG	80176
rs779053735	snp	G/T	3.33567e-05	0.00408378	synonymous-codon	SPSB1	GRCh38.p7	1:9367503	GCGCCTGGCCCTGGG[G/T]AGGGAGCGCCTGGGG	80176
rs779077190	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9347717	TCATGCTGTCCCCAG[C/T]ATCTTCATCCTCATG	80176
rs779140777	in-del	-/ACAC			intron-variant	SPSB1	GRCh38.p7	1:9350102	ACGCCTCACATATCT[-/ACAC]ACACACACACACCCC	80176
rs779184465	snp	A/G	1.73363e-05	0.00294412	missense	SPSB1	GRCh38.p7	1:9355929	GGATCAAGACTGTGG[A/G]CATGAGGGACCCCAC	80176
rs779192243	snp	A/C	0.00011651	0.00763162	intron-variant	SPSB1	GRCh38.p7	1:9367436	TGACCTGCAGTTTCT[A/C]TGTCTCCCCAGCCGA	80176
rs779223044	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9301687	AGGAACAAAGTGGTC[A/T]TGGTGGCAGAGATGG	80176
rs779267429	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9357735	TGTGAATGCAGCCCA[C/T]GTGTAGGGGCACCGT	80176
rs779283983	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9305465	TGTTCACGGCTGAGT[A/C]CCCAGTAGTTAGGTC	80176
rs779285070	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9351126	ATCTGGCCCACTGTC[A/T]ATTTTTGTAAATAAA	80176
rs779308142	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9311890	GCCAGATGAAATAGC[G/T]ATGCTCAGACAAAGC	80176
rs779380677	snp	A/G	1.64953e-05	0.00287182	missense	SPSB1	GRCh38.p7	1:9356036	CCCCCTGTGTCCTAT[A/G]ATGTCCAGCTGCTGC	80176
rs779400189	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9320338	TCTGTGTCGCCTCCT[C/G]CATCCCAGCCAGATG	80176
rs779413605	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9295559	GATCCACCCTTCAGT[C/G]GGTCCCTCTGGGCTG	80176
rs779418219	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9310720	AAAAGAGAGACCTGG[A/G]CAGCAGGACCTTGTC	80176
rs779440349	snp	C/T			missense	SPSB1	GRCh38.p7	1:9355991	CTGGATTACTGCAAG[C/T]CCACCCGGCTGGATC	80176
rs779560522	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9362730	CTCTGGGGCTGTGCA[C/T]GTTCACGTGGGCCAC	80176
rs779574614	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9334860	AGATTCACTCATATA[A/G]CATGTATCAAAATGT	80176
rs779582622	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9338207	CTCAGCTCTCCCCTA[C/T]CCCGTTTCTTCAGGC	80176
rs779585725	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9295640	CAGAGCTGGGGAATG[G/T]GGTGGGGGCCTAGCC	80176
rs779613890	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9354297	CGACCCAGCGTGACT[C/G]TCTCCCGGCAGCCAA	80176
rs779614039	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9361961	GACATCTCCCACTGA[A/G]GAGGCATCTTCCATG	80176
rs779655990	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9328283	CCTCCAAACTGTCAT[C/T]CCTCATGATGTTGTG	80176
rs779670965	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9337771	CTCCCTGCTCCCTGC[C/T]TCCGTTCGTTCTCTT	80176
rs779795087	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9318406	GCGGACAGACAGGGA[A/G]TGGGGACAGCGTCCT	80176
rs779799452	in-del	-/GTGG			intron-variant	SPSB1	GRCh38.p7	1:9357149	TGGATGGATGGATGG[-/GTGG]ATGGATGGGTGGATG	80176
rs779837292	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9362132	CCAGCTGGACTCTGC[C/T]GGGAGCTACTCATCG	80176
rs779840998	snp	A/G	1.64879e-05	0.00287118	missense	SPSB1	GRCh38.p7	1:9356352	TCTACCACGATGGCA[A/G]GAACCAGCCAAGCAA	80176
rs779855591	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9316489	GACTTTGATGGGCAC[A/G]TAGGGCAGGGTCCTA	80176
rs779912394	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9336840	CCTCCATCTCCATTT[A/G]TAGTTCTTTCTATAG	80176
rs779912485	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9301321	CATAGTGAGACTCCC[C/T]GCCCCCGCCATCTCT	80176
rs779919286	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9344003	CCGTGTTAGCCAGGA[C/T]GGTCTCGATCTCCTG	80176
rs779920007	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9303658	CAAGGACTGTACCTC[C/G]TCTCTGGAGAAGGGA	80176
rs779929854	in-del	-/AGTG			intron-variant	SPSB1	GRCh38.p7	1:9309301	GAGAGAGAGAGAGAG[-/AGTG]TGTGTGTGTGTGTGT	80176
rs779999812	in-del	-/T			intron-variant	SPSB1	GRCh38.p7	1:9345484	ATGTCTGCTGCTGTC[-/T]GGGTCACCTTTTGGG	80176
rs780020320	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9348740	GGCTGTTCGAAGCTG[A/G]CCGAGGGAGTACGGG	80176
rs780033845	snp	A/G			missense	SPSB1	GRCh38.p7	1:9356426	CCTGACTCCTTCCTG[A/G]TAGCCCTGGACATGG	80176
rs780087291	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9317670	TGTATTTTTTGTAGA[C/G]TTGGGGTTTCACCCT	80176
rs780088098	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9365826	AAGTCAAGGGGAGAC[C/G]GTGGATGAAGCCTCA	80176
rs780104179	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9319351	TGTTGCTCACCAAGG[C/T]GGGGAACACACCCAG	80176
rs780154502	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9322291	CTATTAGCCTCGGTT[G/T]GCAGGTGGGGAAACT	80176
rs780155431	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9330110	GTCAAAGATCAGTGG[C/T]GTAAATAATTGCTAG	80176
rs780177243	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9326266	GTTTATTCCCAGCAC[C/T]ACCCCAAGGGCTGGG	80176
rs780268441	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9325640	CCTGAGGCACAGTGT[A/G]AACAAGACTGAGTTC	80176
rs780332576	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9333611	GCTGGGATTACAAGC[A/G]TGAGCCACCATGCCC	80176
rs780406718	snp	C/T	3.64292e-05	0.0042677	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9367597	CCATCATACCGCCAG[C/T]GCGACAGCCACCTGG	80176
rs780445668	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9312921	CCCAAGAACATGTGT[A/C]CCCTGCAGACACACC	80176
rs780456933	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9303805	CCAGTTGATAAGGGG[A/C]GAACCTGTGATGATT	80176
rs780494144	in-del	-/GT			intron-variant	SPSB1	GRCh38.p7	1:9293936	TGGGTGTGTGTGTGA[-/GT]GTGTCTCTAAGTGCA	80176
rs780522908	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9354526	CTCAAATCTTCTGCT[A/G]CCTTATCCTTCTCCT	80176
rs780593727	in-del	-/C			intron-variant	SPSB1	GRCh38.p7	1:9340155	GCAGGGTGACCAGTT[-/C]CCTCGCCCCTGTAGG	80176
rs780628390	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9321355	CTCTAGACAGCCCGA[C/T]GGCAGGGGGTGGGCT	80176
rs780632729	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9312224	CCAGGCTGCAGTGCT[A/G]TGTTGCTCAGGTTGG	80176
rs780666692	in-del	-/TT			intron-variant	SPSB1	GRCh38.p7	1:9311161	GCGCAGGATAAAGGG[-/TT]TTTTTTTTTTTTTTT	80176
rs780707152	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9312441	AGGTATTATGCACAC[A/G]CCACGCAGTTCGCCT	80176
rs780741834	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9295664	CCTAGCCCGTGGAAG[C/T]CAGCGCTGCCCTCCC	80176
rs780762700	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9353542	TGCAGAGGGGACACC[G/T]CAGCTCTGTAATGGC	80176
rs780767205	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9309303	GAGAGAGAGAGAGAG[A/T]GTGTGTGTGTGTGTG	80176
rs780772506	in-del	-/T			intron-variant	SPSB1	GRCh38.p7	1:9317840	CGAGGGAACCAATTT[-/T]TTTTTTTTTTTTTTT	80176
rs781024724	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9300540	GCCATCATCCACAAA[G/T]AACTTCATTCCTTTT	80176
rs781027185	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9307391	CCATCCACATTCGGC[A/G]TCACCTCCCATCCTC	80176
rs781069104	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9328721	CTTCTGGGCACGTGA[A/G]GATGGTTTTGTCCCA	80176
rs781093393	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9331621	CAGGCGTGAGTCACC[A/G]TGCCTAGCCGGCACT	80176
rs781108857	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9316865	GGCCGGACCTTGTGA[A/C]CTCTCTGAGCCTCAG	80176
rs781110658	in-del	-/TCTTC			intron-variant	SPSB1	GRCh38.p7	1:9306926	TTACTTTTCTTCTTT[-/TCTTC]TTTTTTTTTTTTTTT	80176
rs781193908	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9318774	TCTGGATGTACAGCA[A/G]GACAGGGTCCCTGTC	80176
rs781198477	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9324206	AAGTGGACACCTCTG[A/T]CGCAGCTGGAATGGG	80176
rs781262063	snp	A/C			intron-variant	SPSB1	GRCh38.p7	1:9341094	ATTTCCCTTTTTTCC[A/C]CTTCCCCTTTCTTCC	80176
rs781273138	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9358197	AGGCATGCGCAAACG[C/T]TTACACATTTCTCTT	80176
rs781307845	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9316745	TCTCCAGGGGAGACC[A/G]CCCCGGAAGCGGCAT	80176
rs781318411	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9308366	CATACCCAGGGCCCC[C/T]GGAGCCACGGTGCCC	80176
rs781331910	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9346196	ATGTGTGAGACGGGG[C/T]GGCAGAGGGAGGGAA	80176
rs781388175	in-del	-/C			intron-variant	SPSB1	GRCh38.p7	1:9320406	CCTCCCCCTGCCCTG[-/C]CCCCACGTGTGTGCA	80176
rs781539197	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9359276	ACCGAGCAAAACATT[A/G]GAGGGTGGGGCACTG	80176
rs781548409	snp	G/T	1.81023e-05	0.00300846	utr-variant-5-prime	SPSB1	GRCh38.p7	1:9355863	AGTTTGCCTTGGGAG[G/T]CGGTAAGAAGGTGAA	80176
rs781558030	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9313114	GTTTAAAAAAAGTCA[A/G]GTCCGGGCGCGGTGG	80176
rs781568490	snp	A/G	9.93764e-05	0.00704829	utr-variant-3-prime	SPSB1	GRCh38.p7	1:9367581	CTACCAGTGACGTTC[A/G]CCATCATACCGCCAG	80176
rs781661166	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9324831	CCAGACAGTCGTGTT[C/T]GCGACAAGTCTGTTC	80176
rs781694977	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9301439	TAGGAGGTTGAGGCT[A/G]CAGTGAGCTGTGATT	80176
rs781699536	snp	A/G	1.68709e-05	0.00290434	missense	SPSB1	GRCh38.p7	1:9367520	GGGAGCGCCTGGGGG[A/G]GATCCACACGCTGCC	80176
rs781722173	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9335554	TGGCTCACGCCTGTA[A/G]TCCCAGCACTTCGGG	80176
rs796072769	in-del	-/TT			intron-variant	SPSB1	GRCh38.p7	1:9317855	TTTTTTTTTTTTTTT[-/TT]GAGACCCTGCAGATT	80176
rs796136938	snp	A/T			utr-variant-3-prime	SPSB1	GRCh38.p7	1:9369193	GTACATTACCCCCTT[A/T]TTATTTTGACGGTTT	80176
rs796139779	in-del	-/A			intron-variant	SPSB1	GRCh38.p7	1:9359853	ATGGAAGCCGGGGGG[-/A]GTGGGTGGCGGGGGC	80176
rs796178293	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9351315	CTTGGCCCAAAGGCA[A/G]CGTCCCTCTGTAGGG	80176
rs796221527	in-del	-/GTTATCCCAGCTACCTG			intron-variant	SPSB1	GRCh38.p7	1:9314053	TGGCGGCGGGCACTT[-/GTTATCCCAGCTACCTG]GGAGGCTGAGGCAGG	80176
rs796227368	in-del	-/G			intron-variant	SPSB1	GRCh38.p7	1:9330559	ACATCCTGCCAGCTG[-/G]ACCTTGTGATCTGGA	80176
rs796228916	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9349278	TCTCTGCTTCCCCGA[A/G]CCCAGCCCTCCCGTG	80176
rs796243179	in-del	-/G			intron-variant	SPSB1	GRCh38.p7	1:9294729	AAGAATTTTCTCGTT[-/G]GGGGGGGCTGGGCCC	80176
rs796249043	in-del	-/CCCT			intron-variant	SPSB1	GRCh38.p7	1:9362180	CACCAGGGCCACCCA[-/CCCT]CCCTCCCTCCCTTCC	80176
rs796257097	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9346943	TATAATCGGAAGTCT[C/T]GGGATAGATCACTGT	80176
rs796271010	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9318081	TTGGGGAAACGCAGC[A/G]ATTGTTCTGGGAAGC	80176
rs796305894	in-del	-/TT			intron-variant	SPSB1	GRCh38.p7	1:9330715	TGAACTTTTTTTTTT[-/TT]AATCGTGGTAAAACA	80176
rs796320000	in-del	A/TGTGT			intron-variant	SPSB1	GRCh38.p7	1:9295219	TGTGAGAGTGTGAGT[A/TGTGT]TGTGTGTGTGTGTGT	80176
rs796324438	snp	C/G			intron-variant	SPSB1	GRCh38.p7	1:9334700	CTGGCACTGACCCCC[C/G]ATTCCTGCTCCCCGG	80176
rs796371090	in-del	-/T			intron-variant	SPSB1	GRCh38.p7	1:9347422	GGAATACATGCATTT[-/T]AAAAAATTCAATTCA	80176
rs796406946	in-del	-/GAGAGAGAGAGTGTGTGTGTGT			intron-variant	SPSB1	GRCh38.p7	1:9309292	AGAGTGTGAGAGAGA[-/GAGAGAGAGAGTGTGTGTGTGT]GTGTGTGTGTGTGTG	80176
rs796465223	in-del	-/TGGATGGG			intron-variant	SPSB1	GRCh38.p7	1:9357154	GGATGGATGGGTGGA[-/TGGATGGG]TGGATGGATGGGTGG	80176
rs796466369	snp	A/T			intron-variant	SPSB1	GRCh38.p7	1:9295221	GTGAGAGTGTGAGTG[A/T]GTGTGTGTGTGTGTG	80176
rs796496495	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9357105	TGGATGGATGGATGG[A/G]TGGATGAGTGGATGG	80176
rs796523569	in-del	A/CCC			intron-variant	SPSB1	GRCh38.p7	1:9325228	CTCCCACCACCACCC[A/CCC]CCCCCCGCCCCGCCT	80176
rs796528181	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9345506	CCTTTTGGGAAGGTT[G/T]CTGTGTGTCCCTGGG	80176
rs796545013	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9357129	TGGATGGATGGATGG[A/G]TGAGTGGATGGATGG	80176
rs796557373	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9357132	ATGGATGGATGGATG[A/G]GTGGATGGATGGATG	80176
rs796603480	in-del	CT/TTCTTC			intron-variant	SPSB1	GRCh38.p7	1:9306925	TTACTTTTCTTCTTT[CT/TTCTTC]TTTTTTTTTTTTTTT	80176
rs796606241	multinucleotide-polymorphism	CT/TC			intron-variant	SPSB1	GRCh38.p7	1:9310140	ATCTGTGATGATGCC[CT/TC]TGCACCTGCCGTGGG	80176
rs796631386	in-del	ACCCCCCCCCCCCG/CCCGCCC			intron-variant	SPSB1	GRCh38.p7	1:9325225	TGCCTCCCACCACCA[ACCCCCCCCCCCCG/CCCGCCC]CCCGCCTCCACCGGT	80176
rs796636039	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9316092	CGGCACAGTGGTCTC[C/T]GGGTCCTGCTGAGGG	80176
rs796643090	in-del	-/TT			intron-variant	SPSB1	GRCh38.p7	1:9317838	TGGCGAGGGAACCAA[-/TT]TTTTTTTTTTTTTTT	80176
rs796659402	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9307862	CCATGATGTGGTCTT[C/T]GGGGTGCGCGTGGCC	80176
rs796675281	snp	G/T			intron-variant	SPSB1	GRCh38.p7	1:9345412	GTGTTACCCGCCGAG[G/T]CTAGGCAGTGTCGGT	80176
rs796678906	in-del	-/GTGTGAGTGTGT			intron-variant	SPSB1	GRCh38.p7	1:9295212	TGTGTGTGTGTGAGA[-/GTGTGAGTGTGT]GTGTGTGTGTGTGTG	80176
rs796680132	in-del	A/GTGTG			intron-variant	SPSB1	GRCh38.p7	1:9348959	GTGTGTGTGTGTGTG[A/GTGTG]ATATGTGCGTGTGTG	80176
rs796704984	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9318648	AGGATTGACCAAAGC[C/T]AGACCGTGTGGCTGG	80176
rs796705662	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9335750	AAGGTTGAGCCTGCA[A/G]TGAGCCATGATCGTG	80176
rs796740399	in-del	-/T			intron-variant	SPSB1	GRCh38.p7	1:9311161	GCGCAGGATAAAGGG[-/T]TTTTTTTTTTTTTTT	80176
rs796749551	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9357112	ATGGATGGATGGATG[A/G]GTGGATGGATGGATG	80176
rs796775799	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9297710	AAAGGATGACCCACT[A/G]TGAGTAAGTTGGAGT	80176
rs796812633	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9357104	GTGGATGGATGGATG[A/G]ATGGATGAGTGGATG	80176
rs796813058	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9361160	TCTGTCATTTTCTTT[C/T]TTTTTTTTTTTTTTT	80176
rs796839582	in-del	-/T			intron-variant	SPSB1	GRCh38.p7	1:9330945	TGCGTCTTTTTTTTT[-/T]ACATACTTAAAAAAA	80176
rs796883882	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9357113	TGGATGGATGGATGA[A/G]TGGATGGATGGATGG	80176
rs796896502	snp	A/G			intron-variant	SPSB1	GRCh38.p7	1:9314594	CTGGTAAATCACACA[A/G]AGAATTGCAGAAAGT	80176
rs796930232	in-del	-/TGAATGAA			intron-variant	SPSB1	GRCh38.p7	1:9298455	AAGTGAATGAATAAG[-/TGAATGAA]TGAATGAATGAATTG	80176
rs796985525	in-del	-/CAG			intron-variant	SPSB1	GRCh38.p7	1:9317191	AGGGTTTACTCTCAG[-/CAG]GTGAATCTGGGAAGG	80176
rs797015177	snp	C/T			intron-variant	SPSB1	GRCh38.p7	1:9325236	CACCACCCCCCCCCC[C/T]CGCCCCGCCTCCACC	80176
rs797021031	in-del	-/T			intron-variant	SPSB1	GRCh38.p7	1:9330705	CATGTTCTTCTGAAC[-/T]TTTTTTTTTTTAATC	80176

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