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

SCAP

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs369532437	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47460645	GCAACCTCTGCCCCC[C/G]CCCCCAGGTTCAAGC	22937
rs369534719	snp	A/C	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47463021	TCCCCTAAGCTCCTT[A/C]TTTACACTATTTCCA	22937
rs369575225	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47473270	ACAGTGTTATCTCAC[C/T]TGGTTATTATGAAAA	22937
rs369613727	snp	A/C	0.00119737	0.0244387	intron-variant	SCAP	GRCh38.p7	3:47474089	GCTAACACGGTGAAA[A/C]CCCGTCTCTACTAAA	22937
rs369625216	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47459536	ACAGCTGGGCCTCCA[A/G]GGGTGACATCACATA	22937
rs369635500	snp	G/T	1.8635e-05	0.0030524	intron-variant	SCAP	GRCh38.p7	3:47419732	AGGGGGTACTCAGTG[G/T]GAGGAATGGGCCCCA	22937
rs369719720	snp	A/C	0.000169986	0.00921759	missense	SCAP	GRCh38.p7	3:47417503	CAGACGGCCGCCAGC[A/C]CCTCCTCCTGGTACA	22937
rs369739992	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47447676	CCTGGGCAATACAGC[A/G]AGACTCTGACTCAAA	22937
rs369811317	snp	C/G/T	0.000118054	0.00768207	utr-variant-5-prime, missense, intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47426146	TGCAGAAGCATCAGG[C/G/T]GGGCACGCAGGCTGC	22937
rs369825023	snp	C/G			intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47426288	TGTGTTGAAAGGGAA[C/G]TTCTCTATGGTGCCT	22937
rs369867832	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47441799	AAATGGAAACATAAC[C/T]GGACCACTTCCTAAT	22937
rs369868152	snp	A/T			intron-variant	SCAP	GRCh38.p7	3:47459109	CGTACCCAGCCAAGA[A/T]TCTGTTTTAAAGCTA	22937
rs369891654	in-del	-/T			intron-variant	SCAP	GRCh38.p7	3:47459468	CTTTCTATTTTCCGT[-/T]AAGTGTCGGCCGGCT	22937
rs369991877	snp	A/T	6.31772e-05	0.00562002	synonymous-codon	SCAP	GRCh38.p7	3:47418693	GGCCTGCACCCCACC[A/T]GGGCCCTTGGGTCCT	22937
rs369999463	snp	A/C	0.000153988	0.00877328	intron-variant	SCAP	GRCh38.p7	3:47414547	ACAGACTCTGTACCC[A/C]CTACCCCACCTGCAG	22937
rs370057884	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47464830	CAGGAAGTAGTAAAA[C/T]TATTTCCGTTCCTAG	22937
rs370068193	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47478892	ATTCCCGTGCCTCAA[C/T]CTCTTGAGTAGCTGG	22937
rs370092118	snp	C/G	9.51158e-05	0.00689557	intron-variant	SCAP	GRCh38.p7	3:47418263	TCCTGCAGAAGCCCG[C/G]TGTTGGTATGGGCCA	22937
rs370170846	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47421088	CTGTCCCAGCCCAAG[A/G]GGAGCAGTACCCGGA	22937
rs370196779	snp	A/G	0.000153988	0.00877328	missense	SCAP	GRCh38.p7	3:47420691	TCACAGCCAGCTGCC[A/G]CTCGTAGCGCGTTGG	22937
rs370224030	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47466172	AGAAAGAAATTCTCC[C/T]CATTACTTTGTCCAA	22937
rs370276700	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47416191	GAGCCAGTGTGGGAC[A/G]GGCAGGCAAAGGCGT	22937
rs370283515	snp	C/T	3.3355e-05	0.00408367	missense	SCAP	GRCh38.p7	3:47420694	CAGCCAGCTGCCGCT[C/T]GTAGCGCGTTGGCTG	22937
rs370325588	snp	A/G	0.00119737	0.0244387	intron-variant	SCAP	GRCh38.p7	3:47473292	TTATGAAAACTAAGT[A/G]AGATAAGCTAATATT	22937
rs370331755	snp	A/G	0.000356189	0.0133404	missense	SCAP	GRCh38.p7	3:47418370	TCCGTCTCGGGTGGC[A/G]CATAGCCGTAGTCGT	22937
rs370396440	snp	C/T	3.42179e-05	0.00413615	intron-variant, utr-variant-3-prime, downstream-variant-500B	PTPN23, SCAP	GRCh38.p7	3:47413826	ACACAGCACCCCAGC[C/T]TCCTGCCTGGGCAAG	22937
rs370402279	snp	C/T	0.000153988	0.00877328	missense, intron-variant, synonymous-codon	SCAP	GRCh38.p7	3:47425486	TGCTAGGGACCTACC[C/T]GCCATTGAGGGTGGG	22937
rs370538144	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47438463	GGGCTGCTCTGCCTA[C/T]GGAGCAGCCATTCTT	22937
rs370577835	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47436206	GATAGCTAAGCAACT[A/G]TTCCACTTAAAGGGA	22937
rs370657900	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47431264	GTGAACTCCCACAAT[A/C]CCTACTTTACAGCAC	22937
rs370669976	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47453372	ACATAGTGAGACCCC[A/G]TCTCTTTAAAAAAAA	22937
rs370739539	snp	A/G	9.15688e-05	0.0067658	synonymous-codon	SCAP	GRCh38.p7	3:47418762	CCAGGCACTGCGGCC[A/G]TCCTGAGGGTGCCGG	22937
rs370787242	snp	C/T	1.67643e-05	0.00289515	synonymous-codon	SCAP	GRCh38.p7	3:47420641	GTTTCGGAAGGAAGA[C/T]GGCTGCAACGTGATG	22937
rs370895515	snp	A/C/T	9.96661e-05	0.00705855	synonymous-codon	SCAP	GRCh38.p7	3:47418345	GCCGCGCAGCACAAG[A/C/T]GGCACGATCTCCGTC	22937
rs370907919	snp	C/T	3.29462e-05	0.00405857	intron-variant, missense, upstream-variant-2KB, utr-variant-5-prime	SCAP	GRCh38.p7	3:47427527	GGATCAGCATGGAAG[C/T]GTTCCCAGTCATTCT	22937
rs370924458	in-del	-/TC	0.00478085	0.0486577	intron-variant	SCAP	GRCh38.p7	3:47448517	ATAAAAGATAAACTT[-/TC]TGTTATTGTCCCATG	22937
rs370945458	in-del	-/TG			intron-variant	SCAP	GRCh38.p7	3:47467766	GCCCTTGGGTACATG[-/TG]CACAACATACAGGTT	22937
rs370993634	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47446117	TTGACCTCGTGATCT[A/G]ACCGCCTCAGCCTCC	22937
rs371009060	snp	A/G	0.000187063	0.00966935	intron-variant	SCAP	GRCh38.p7	3:47415206	AGAACAGCTGCCAGG[A/G]GCCTCTCCCTTAGAG	22937
rs371112748	in-del	-/TT	0.00159617	0.0282053	downstream-variant-500B	PTPN23, SCAP	GRCh38.p7	3:47413490	AGCACTGCCAGGAAC[-/TT]TTAACTTACTTAGCA	22937
rs371125960	snp	A/G	0.000104763	0.00723676	intron-variant	SCAP	GRCh38.p7	3:47414789	CTCCCACCCCGTGCC[A/G]GGCCACTCCAGCACC	22937
rs371169044	snp	C/G/T	0.00032002	0.012646	intron-variant	SCAP	GRCh38.p7	3:47417273	CCCGGGGCGGACAGC[C/G/T]GCTCTGCCCACCTTT	22937
rs371191559	in-del	-/T			intron-variant	SCAP	GRCh38.p7	3:47455094	ATATATATATATATA[-/T]AATCAACTGAAAACC	22937
rs371191984	snp	G/T	0.00398564	0.0444627	intron-variant	SCAP	GRCh38.p7	3:47456362	GAGCCATGATCACAC[G/T]ACTGTGCTCCAGTAT	22937
rs371236737	snp	A/C/G	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47437636	CTGTAGTCCCAGCTC[A/C/G]GGAGGCTTAAGTGGG	22937
rs371256605	snp	A/G	8.66183e-05	0.0065804	intron-variant	SCAP	GRCh38.p7	3:47417255	CCAGAAAGGCCCACA[A/G]TCCCCGGGGCGGACA	22937
rs371270622	snp	A/C/G	3.321e-05	0.00407482	intron-variant	SCAP	GRCh38.p7	3:47421053	AGAGCACATGGGGAT[A/C/G]GGGGGGTGCCGTGAC	22937
rs371278732	snp	C/T	1.66272e-05	0.00288328	intron-variant	SCAP	GRCh38.p7	3:47414695	GGTCTCTGGGATTTT[C/T]CAAGTTATACTTTGG	22937
rs371357640	snp	A/G	4.95593e-05	0.00497767	synonymous-codon, intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47426061	GGGGATGAGCTCAGC[A/G]ACACCAATCTCCTCC	22937
rs371384070	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47430711	CTGTAAAGACTCCCC[A/G]GGAGTTGGTGACAAC	22937
rs371384098	snp	C/G/T	0.000101081	0.00710856	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47426203	GGGGGTAAATGGAAG[C/G/T]GTTGCTCTTGGTTCT	22937
rs371389974	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47471709	TCTGAAAATGCTAAA[C/T]ATCAAATAAGCCACT	22937
rs371413325	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47460819	CCTCGACCTCCCAAA[C/G]TGCTGGGATTACAGG	22937
rs371442435	snp	A/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47460467	AAATCTTCACCATTT[A/T]TGTTCCTCTGCCGCG	22937
rs371492665	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47473761	ATACCTGCAGTGAAG[C/T]CCACAGGCACACTTT	22937
rs371530031	in-del	-/CTG			intron-variant	SCAP	GRCh38.p7	3:47422291	GGGGCCATCTGGGTG[-/CTG]TAGTGATCTGCTTGC	22937
rs371639097	snp	A/G	0.00795532	0.062565	intron-variant	SCAP	GRCh38.p7	3:47457704	CGAGGTCAGGAGATC[A/G]AGACCATCCTGGCTA	22937
rs371639379	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47423361	GGGCCTAGTGTGCTG[C/G]AGTGAGGCAGTAAGA	22937
rs371749768	snp	A/G	1.67435e-05	0.00289335	synonymous-codon	SCAP	GRCh38.p7	3:47414357	CAGGCAGATGGCCCC[A/G]TCTTGTCCTCCACTG	22937
rs371768067	snp	A/G	0.000628119	0.0177106	missense	SCAP	GRCh38.p7	3:47418413	CCCCGCGCCTCCGCC[A/G]CCCGGGCCCACCACC	22937
rs371803846	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47446991	GTTAATTTTTAGATA[A/G]GGTGTGAGATATAAA	22937
rs371809207	snp	A/G	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47447388	ACAGACTGTGACTCC[A/G]TCTCAAAAAAGGAGA	22937
rs371849082	snp	C/T	9.33228e-05	0.00683028	synonymous-codon	SCAP	GRCh38.p7	3:47418513	GGTGGCCAGGCCCAG[C/T]GCCGCCACCCTGCAC	22937
rs371865910	snp	C/G	2.17092e-05	0.00329456	intron-variant	SCAP	GRCh38.p7	3:47427698	GACAAGGCACCTGCT[C/G]TGTCTGCCACCACAG	22937
rs371905128	snp	G/T			intron-variant	SCAP	GRCh38.p7	3:47448724	AATTTCTGATTTTCT[G/T]TTCATTTCAAGAGCA	22937
rs371906022	snp	C/T	3.31549e-05	0.0040714	missense	SCAP	GRCh38.p7	3:47414072	GGTTGTCTGAGATGA[C/T]ACCCAAGCTTGCACC	22937
rs371920447	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47478011	CTGATCCCTTGAAAT[A/G]CCATCATTTGTCCCC	22937
rs371942334	snp	A/G	0.000131994	0.00812277	synonymous-codon	SCAP	GRCh38.p7	3:47421009	AGACACCAGCCCCAC[A/G]ACAGCAAAGAGACAG	22937
rs371988682	snp	C/T	0.0001953	0.00987988	intron-variant	SCAP	GRCh38.p7	3:47419315	AGGTGGCACCTGGCA[C/T]GGCCCAGCTCACCTC	22937
rs371997320	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47457192	CAGCACCAGCAGCCT[C/T]TGGGGAGAGGATCTG	22937
rs372044719	snp	A/G	3.30311e-05	0.0040638	missense	SCAP	GRCh38.p7	3:47413952	GCACCAGGATCTGGC[A/G]GGCAGGCTGGGCCTC	22937
rs372058889	snp	A/G	3.90633e-05	0.00441929	synonymous-codon	SCAP	GRCh38.p7	3:47418476	GGTAGAGGCAGAGCA[A/G]CAGCAGCACCAAGAC	22937
rs372087332	in-del	-/C			intron-variant	SCAP	GRCh38.p7	3:47443464	GCATTCTTCCCCCCC[-/C]TCCTCTATGCACAAA	22937
rs372158341	snp	A/G	0.000179984	0.0094847	missense	SCAP	GRCh38.p7	3:47417474	CAGGCGAGGGTGGGC[A/G]CAGGGCTGGTGTGCA	22937
rs372172424	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47464101	GCTCACTGCAACCTC[C/T]GCCTCCCAGGTTCAA	22937
rs372178337	snp	C/G	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47431054	TTAGTGAGGGCTCTG[C/G]GGACAGAAGGCCTCA	22937
rs372186566	snp	A/G	0.000170847	0.0092409	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47425962	ATGCCCGTTTAGCTT[A/G]GAGAAAGCCCTCAGC	22937
rs372202283	snp	C/T			upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47478173	ACTGCTGTCATTCTC[C/T]TCACTCACCACCTCT	22937
rs372219013	snp	A/T			intron-variant	SCAP	GRCh38.p7	3:47443268	CACACACACACACAC[A/T]CACACACACTCTCTC	22937
rs372307441	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47472941	CAAAATTAGCCAGGC[A/G]TGGTAGTGCATGCCT	22937
rs372311997	snp	C/T	1.6941e-05	0.00291036	missense	SCAP	GRCh38.p7	3:47414871	CCAAGCGCCCAGCAG[C/T]GGCTTTCAGGGCTGT	22937
rs372329422	snp	C/T			upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47477463	GTAGTCCCAGCTACT[C/T]GGGAGGCTGAAGCAG	22937
rs372346811	snp	C/T	0.000208109	0.0101986	intron-variant	SCAP	GRCh38.p7	3:47415094	CCACCCCAGGCCCTC[C/T]GACCTCTAAACTGCA	22937
rs372360550	snp	C/G	8.42112e-05	0.00648834	intron-variant	SCAP	GRCh38.p7	3:47428710	GAAAGGGCAGCTGAG[C/G]ACAGGAAGAAGAAAG	22937
rs372403065	in-del	-/G			intron-variant	SCAP	GRCh38.p7	3:47432333	AAAAAAAAAAAAAAA[-/G]AAAAGAAAAAGGAAA	22937
rs372404136	snp	C/T	0.00199481	0.0315187	intron-variant	SCAP	GRCh38.p7	3:47455806	AACAAACTTCAAGTT[C/T]ATACAGAAAAACAAA	22937
rs372447767	in-del	-/T			intron-variant	SCAP	GRCh38.p7	3:47455086	ATATATATATATATA[-/T]ATATATATAATCAAC	22937
rs372472350	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47460500	TCCAGCCAGTCCCTC[C/T]GTTCGGGGTCCCTGA	22937
rs372516316	snp	C/T	1.64958e-05	0.00287187	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47427404	AAAGACGGTGACCAA[C/T]GGGCACCTTTACAGG	22937
rs372590558	snp	C/T	0.000117179	0.00765349	synonymous-codon	SCAP	GRCh38.p7	3:47419363	GTAATAGCTGAAGAG[C/T]GTCGGCCAGTGGCGG	22937
rs372593022	snp	G/T			intron-variant, upstream-variant-2KB	SCAP, LOC105377073	GRCh38.p7	3:47474587	AATGCTTGAGCCCAG[G/T]AGTTAAAGACCAGCC	22937
rs372650663	snp	C/T	3.36525e-05	0.00410184	synonymous-codon	SCAP	GRCh38.p7	3:47420770	CTTGTTCAGGTCTGC[C/T]AGCTGTTGGGGGCAC	22937
rs372668718	snp	A/G	0.000798403	0.0199641	downstream-variant-500B	PTPN23, SCAP	GRCh38.p7	3:47413489	GTAGCACTGCCAGGA[A/G]CTTAACTTACTTAGC	22937
rs372689289	in-del	-/C	0.00233926	0.0341197	intron-variant	SCAP	GRCh38.p7	3:47473366	ACCCAGAATTATTAC[-/C]TCTGAGTGGCAAAAG	22937
rs372710046	snp	C/T			intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47426657	TTAGCCAGGATGGTC[C/T]CGATCTCCTGACCTC	22937
rs372725830	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47447761	CCTGTAATCCCAGCA[C/T]TTTGGGAGGCCAGGG	22937
rs372808233	in-del	-/A	0	0	intron-variant	SCAP	GRCh38.p7	3:47453407	AATGGAAAAAAAAAA[-/A]GACCTGCTTATGTCA	22937
rs372818198	snp	G/T			intron-variant	SCAP	GRCh38.p7	3:47422388	TGGCTGCACAGCTGG[G/T]GAGCACAGCAGTTGC	22937
rs372898041	snp	A/C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47467672	AATGGCCAATCAACA[A/C/T]ATGAAAAATTGCTCA	22937
rs372906472	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47433825	AATGAGCTGAGATCA[C/T]GCCACTGTACTCCAC	22937
rs372926488	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47468965	GATAGTTTCTATGTA[A/G]AATAATGAAAACATT	22937
rs372930525	snp	C/T	1.66078e-05	0.00288161	synonymous-codon	SCAP	GRCh38.p7	3:47414183	CATCCCCTCTACCTG[C/T]TGAATGGAGTAGAAC	22937
rs372969610	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47450146	GGAGTTACAGGCGTG[C/T]GCCACCCCACCCAGC	22937
rs372981910	snp	G/T	6.59065e-05	0.00574012	intron-variant, missense, upstream-variant-2KB	SCAP	GRCh38.p7	3:47427174	GGCATGGTAGTGCTG[G/T]AAGACCAGGGTGATG	22937
rs373009666	in-del	-/C			intron-variant	SCAP	GRCh38.p7	3:47445243	TACCTGTTTTCAATT[-/C]TTTTTTTTTTTTTTT	22937
rs373022065	snp	A/G	8.2464e-05	0.00642069	utr-variant-5-prime, synonymous-codon	SCAP	GRCh38.p7	3:47435083	GTAATCCTTCACAGG[A/G]GTGGTGAATTCCACA	22937
rs373064782	snp	A/C	0.000431775	0.0146868	intron-variant	SCAP	GRCh38.p7	3:47419743	AGTGGGAGGAATGGG[A/C]CCCAACCCCCAGCAG	22937
rs373084496	snp	C/G	0.000153988	0.00877327	utr-variant-3-prime, downstream-variant-500B	PTPN23, SCAP	GRCh38.p7	3:47413216	CTGGTCCTTACACTA[C/G]ATCATCATCATCTCA	22937
rs373086632	snp	A/G	9.30865e-05	0.00682162	intron-variant	SCAP	GRCh38.p7	3:47415204	GAAGAACAGCTGCCA[A/G]GGGCCTCTCCCTTAG	22937
rs373115861	snp	A/G	0.000224167	0.0105846	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47425659	CCTCCCCCAGCCCCC[A/G]GCCCACTGGGGCTCC	22937
rs373135135	snp	C/T	1.65982e-05	0.00288077	intron-variant	SCAP	GRCh38.p7	3:47414551	ACTCTGTACCCCCTA[C/T]CCCACCTGCAGGCCG	22937
rs373142161	snp	A/G	0.000153988	0.00877328	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47427109	ACTACTCAAAGCCTC[A/G]TGTCACCCAGCAGAC	22937
rs373159378	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47455627	AAAAAGAAACCAAAA[A/G]AAATCTCTGAAACTC	22937
rs373163455	snp	A/G	0.000153988	0.00877327	synonymous-codon	SCAP	GRCh38.p7	3:47418744	TATGGGCCCCGGTGG[A/G]GGCCAGGCACTGCGG	22937
rs373167143	snp	C/G/T	1.75634e-05	0.00296334	synonymous-codon, missense	SCAP	GRCh38.p7	3:47419618	CTCACCCAATGGGCT[C/G/T]TGTTCCGTCACCTGG	22937
rs373169850	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47423155	ATGGACGGCTGCCTA[C/T]AGCCCCATTCCTCAC	22937
rs373299249	snp	G/T			intron-variant	SCAP	GRCh38.p7	3:47435557	ATCCAGGTAATTTTT[G/T]TATTTTTAGTGGAGA	22937
rs373304395	snp	C/T	0.00431117	0.0462277	intron-variant	SCAP	GRCh38.p7	3:47418125	GGAGGAAAGGGCAGC[C/T]GCACCTACCCTGGGC	22937
rs373310433	snp	G/T			intron-variant	SCAP	GRCh38.p7	3:47433270	ACAGCCAATGGAGGT[G/T]AGATAACTGACCACT	22937
rs373322375	snp	C/T	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47434655	CCAGCTTGGCCAACA[C/T]AGTGAAACTCCATCT	22937
rs373327410	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47474159	AGTCCCAGCTACTTG[A/G]GAGGCTGAGGCAGGA	22937
rs373405376	snp	C/G			synonymous-codon	SCAP	GRCh38.p7	3:47420587	CAGGCGGGTGCGGGC[C/G]AGGAAGTAGACAACA	22937
rs373470095	snp	A/G	4.97731e-05	0.00498839	missense	SCAP	GRCh38.p7	3:47419377	GCGTCGGCCAGTGGC[A/G]GAAGGACAATTTCCT	22937
rs373474160	in-del	-/CA			intron-variant	SCAP	GRCh38.p7	3:47465586	CCAGCCTGGGCAACA[-/CA]GTGAGACTCCATCTC	22937
rs373538536	snp	C/G	0.000100822	0.00709934	intron-variant	SCAP	GRCh38.p7	3:47418273	GCCCGGTGTTGGTAT[C/G]GGCCAGGCTCCGGCC	22937
rs373544490	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47460486	TCCTCTGCCGCGGCT[C/T]CAGCCAGTCCCTCCG	22937
rs373600832	in-del	-/C	0.00478085	0.0486577	intron-variant	SCAP	GRCh38.p7	3:47452311	GGACAATCCCTTGAG[-/C]CCAGGAGTTTGATGC	22937
rs373651200	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47432357	AAGGAAAAAAAAAAA[A/G]AAAAAAAAATTGCTC	22937
rs373671454	snp	C/G			upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47478113	GGGTCAGGAGCCTGT[C/G]TTTTAACCACCTCCA	22937
rs373732427	snp	C/T	0.000437904	0.0147905	upstream-variant-2KB, intron-variant, nc-transcript-variant	SCAP, LOC105377073	GRCh38.p7	3:47476698	GGCCCTCCTGAAAAT[C/T]CGAGGTAGGTCTTGT	22937
rs373741294	snp	A/C/T	0.000329639	0.0128348	missense	SCAP	GRCh38.p7	3:47418383	GCGCATAGCCGTAGT[A/C/T]GTCGCAGGGCAGCTC	22937
rs373786937	snp	C/T	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47468181	GCCGTAATAAACATA[C/T]GTGTGCATGTGCCTT	22937
rs373817743	snp	A/G	0.00199481	0.0315187	intron-variant	SCAP	GRCh38.p7	3:47440187	CCCAGGAACAATAAA[A/G]GGTAAGCAATTAAAT	22937
rs373891396	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47447010	GTGAGATATAAATTC[C/T]TTTTTTTCCCCTTTG	22937
rs373949576	snp	A/G	1.67103e-05	0.00289048	synonymous-codon	SCAP	GRCh38.p7	3:47417169	TGAGGAGACCTCCTC[A/G]CTGCTGCAGCACAGC	22937
rs373996520	snp	A/T			intron-variant	SCAP	GRCh38.p7	3:47425190	ACACACATGCAATAC[A/T]TACTCATGTATACAC	22937
rs374000283	in-del	-/TT			intron-variant	SCAP	GRCh38.p7	3:47415761	ATGGGGTTCAAAATC[-/TT]ACTGCAGGGAAAGGC	22937
rs374083383	snp	C/G	3.36819e-05	0.00410364	missense	SCAP	GRCh38.p7	3:47414926	CACTGTGTGGGTCAG[C/G]TGACAGGCCACTGTG	22937
rs374089255	snp	A/G	0.000153988	0.00877328	intron-variant	SCAP	GRCh38.p7	3:47422432	CAGGTGGCAGGCCTT[A/G]GGGCCTTACCTGGAT	22937
rs374090479	snp	C/T	9.52789e-05	0.00690148	missense	SCAP	GRCh38.p7	3:47417315	CCACCTCCAGCCGGC[C/T]GCTGCTCCGCCCCAC	22937
rs374097434	snp	C/G			intron-variant, upstream-variant-2KB	SCAP, LOC105377073	GRCh38.p7	3:47475243	TGCAACTAACGCTAT[C/G]GTGACATTATAAGCC	22937
rs374098174	in-del	-/ACTTA			downstream-variant-500B	PTPN23, SCAP	GRCh38.p7	3:47413498	CAGGAACTTAACTTA[-/ACTTA]CTTAGCACCTTTTGT	22937
rs374110557	snp	A/C	6.88255e-05	0.00586583	synonymous-codon	SCAP	GRCh38.p7	3:47418801	AGCCTCCCTCGGGTT[A/C]AGGCGGAGCGTGACT	22937
rs374183763	snp	A/G	0.000132868	0.00814963	intron-variant	SCAP	GRCh38.p7	3:47414656	CAGACGGAACACCTG[A/G]GACAGGGATGGGCCT	22937
rs374284206	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47452893	AGGAAAGTTCAAGAC[C/G]AGCCTGGGCAACATA	22937
rs374307365	snp	G/T			intron-variant	SCAP	GRCh38.p7	3:47452002	CTCTTTATAGGCTGG[G/T]TCCTTTTCATTCTTC	22937
rs374318135	snp	C/G			upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47478732	ATCCACCCGCCTCAG[C/G]CTCTCAAAGTGCTGG	22937
rs374434485	snp	G/T			intron-variant	SCAP	GRCh38.p7	3:47415630	CAAGCACAGCTCACA[G/T]CAATTCCTTTTTCCA	22937
rs374484467	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47471867	ATAATAAAAATTATT[A/G]TGGTGGTTCATGCCT	22937
rs374485012	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47437699	ATAAGCCATGATCAT[C/G]CCACTGCATTCCAGC	22937
rs374556340	snp	C/T	0.0119091	0.0762411	intron-variant	SCAP	GRCh38.p7	3:47448091	AAATTTGCAAAGAAC[C/T]GGCATGTTGAGTCTT	22937
rs374671609	snp	C/T	2.13709e-05	0.00326879	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47426210	AATGGAAGTGTTGCT[C/T]TTGGTTCTGGGGACA	22937
rs374675395	snp	A/G	5.84983e-05	0.00540793	missense	SCAP	GRCh38.p7	3:47417324	GCCGGCCGCTGCTCC[A/G]CCCCACCACGATGAG	22937
rs374695635	snp	C/G/T	0.000256152	0.0113143	intron-variant, utr-variant-3-prime, downstream-variant-500B	PTPN23, SCAP	GRCh38.p7	3:47413830	AGCACCCCAGCCTCC[C/G/T]GCCTGGGCAAGGAGG	22937
rs374707747	snp	C/T	0.000177384	0.00941596	synonymous-codon	SCAP	GRCh38.p7	3:47418453	GTAGTTGCGCGGGCA[C/T]AGCACGCGGTAGAGG	22937
rs374777441	snp	C/G	5.02904e-05	0.00501425	intron-variant	SCAP	GRCh38.p7	3:47428499	AGGGAGGCCAGGGTC[C/G]CTGAGAGGGGTACCT	22937
rs374847192	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47478468	ATGATTTTTGGGCTT[C/T]TCCCACAACATTTTT	22937
rs374873133	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47430756	CATGGCCCTAGACAG[C/T]GGTGTACTGCGAGGT	22937
rs374883549	snp	A/G	5.01542e-05	0.00500745	synonymous-codon	SCAP	GRCh38.p7	3:47420659	CTGCAACGTGATGGT[A/G]TGGGGTGTGGACGGC	22937
rs374985943	snp	A/G/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47436404	TGGGAGAGGCCAAGC[A/G/T]GGCGGATCATTTGAG	22937
rs375040802	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47451949	TCATTCCCATCTCAG[A/G]GGCCTGGCACATACT	22937
rs375084370	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47431265	TGAACTCCCACAATC[A/C]CTACTTTACAGCACA	22937
rs375101973	snp	C/T	0.00159617	0.0282053	intron-variant	SCAP	GRCh38.p7	3:47473145	TAAAAGGATGGACTC[C/T]TTTGTCAGCCAAATC	22937
rs375178561	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47445243	TACCTGTTTTCAATT[C/T]TTTTTTTTTTTTTTT	22937
rs375312998	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47471306	ACAATCACAGTAATA[C/T]TTAGAACGGGAAGGA	22937
rs375393152	snp	C/G	1.86367e-05	0.00305254	intron-variant	SCAP	GRCh38.p7	3:47419731	CAGGGGGTACTCAGT[C/G]GGAGGAATGGGCCCC	22937
rs375402116	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47420223	CACCATGCAGCGGCC[A/G]ATGAACCCGACCCAG	22937
rs375407546	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47418559	TGTGAGACACACCTC[A/G]CAGCCTGTCCCCTCC	22937
rs375413175	snp	A/C/G	5.17516e-05	0.00508661	missense	SCAP	GRCh38.p7	3:47415167	GGGAACCGTTGAGCC[A/C/G]TGCAGCCACAATCCT	22937
rs375418289	snp	A/G	0.000544649	0.0164933	intron-variant, utr-variant-5-prime	SCAP	GRCh38.p7	3:47434971	CAGTCTCCACCCAAC[A/G]CTCTGTGCTGGCCTC	22937
rs375420396	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47454652	GAGAATCGCTTGAAC[A/G]CAGGAGAATCGCTTG	22937
rs375455456	snp	A/G	0.000150475	0.00867266	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47425624	TCCCTGGAGGGCAGA[A/G]AGGGCGTATCAGGGC	22937
rs375462057	snp	C/T			intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47426230	TTCTGGGGACAAAGA[C/T]AATCCCCGGACAGAG	22937
rs375611473	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47467889	CCTCCCCCCATCCCC[C/T]GGCAGGCCCTGGTGA	22937
rs375612610	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47437483	AGGTGGCTCATGCCT[A/G]TAATCCCAGCACTTT	22937
rs375622474	snp	A/G/T	9.96573e-05	0.00705835	synonymous-codon, intron-variant	SCAP	GRCh38.p7	3:47423940	TGCGTTACCTTGGGC[A/G/T]ATCCGCAGCTTCACC	22937
rs375737763	snp	A/G	1.67728e-05	0.00289588	missense	SCAP	GRCh38.p7	3:47419560	GGTCCGGGTGGCTGG[A/G]GGGCAGCATGCCACT	22937
rs375750126	in-del	-/A			intron-variant	SCAP	GRCh38.p7	3:47449347	AAAGTCAGGGGTTTA[-/A]TTTCCCTAACCTGCT	22937
rs375803328	snp	A/G	0.000201261	0.0100295	intron-variant	SCAP	GRCh38.p7	3:47423928	CAACTCTCCCACTGC[A/G]TTACCTTGGGCGATC	22937
rs375862878	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47476039	GTCGAACCACATTCG[A/C]GTCTCCCGTTCGCCC	22937
rs375863599	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47466068	AACCCAGGAGGTGGA[A/G]TTTGCAGTGAGCCAA	22937
rs375877970	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47463474	TGGGAGGCAGAGGCA[A/G]GCGGATCACTTGAGG	22937
rs375881587	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47463423	ACACTCCAGTGGGCC[A/G]GGGTGCGGTGGCTCG	22937
rs375902501	snp	A/G	1.66021e-05	0.0028811	intron-variant	SCAP	GRCh38.p7	3:47414541	TGGGCCACAGACTCT[A/G]TACCCCCTACCCCAC	22937
rs375911801	snp	A/G	3.29527e-05	0.00405898	intron-variant, synonymous-codon, upstream-variant-2KB, utr-variant-5-prime	SCAP	GRCh38.p7	3:47427231	GTAGAGGCTCACCCC[A/G]CTGTACTTCCCAGGA	22937
rs375960354	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47459772	CACGTATTGTCTTGA[C/T]AAACATCTTAAACAA	22937
rs375974703	snp	C/T			intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47426688	ATGATCCGCCTGCCT[C/T]GGCCTCCCAAAGTCT	22937
rs375979759	in-del	-/CCTGGCACATA			intron-variant	SCAP	GRCh38.p7	3:47449178	AAAGCCTTTGGTATG[-/CCTGGCACATA]CTGTTTAGGGTCAGA	22937
rs376014393	snp	A/G	9.49532e-05	0.00688967	missense	SCAP	GRCh38.p7	3:47418358	AGCGGCACGATCTCC[A/G]TCTCGGGTGGCGCAT	22937
rs376033338	snp	A/C	0.000355604	0.0133295	intron-variant	SCAP	GRCh38.p7	3:47423921	CTCTGCCCAACTCTC[A/C]CACTGCGTTACCTTG	22937
rs376057382	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47465841	ACTTGTTTAAAAAAA[A/C]AAAAAAAAAAAAGCT	22937
rs376064054	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47434761	AGAATCACTTGAACC[C/T]GGGAGGCGGAGGTTG	22937
rs376083345	snp	C/T	3.29457e-05	0.00405854	intron-variant, missense, upstream-variant-2KB, utr-variant-5-prime	SCAP	GRCh38.p7	3:47427495	GCTCGTGCTGGTGGA[C/T]GGTCCCAATGATGTC	22937
rs376114087	snp	C/T	9.14788e-05	0.00676247	missense	SCAP	GRCh38.p7	3:47418757	GGGGGCCAGGCACTG[C/T]GGCCGTCCTGAGGGT	22937
rs376146625	snp	A/T			intron-variant	SCAP	GRCh38.p7	3:47443611	GGTCAGCCCTCAACA[A/T]AAAAACGCTAAAAAG	22937
rs376158944	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47440319	GCTCTGGACAGAAAA[A/G]CTTCAGTGGGTTGAA	22937
rs376275596	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47445491	AACCAGGTGATCCAC[C/T]GCCTCGGCCTCCCAA	22937
rs376295408	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47444032	ATCAACTTTTTTTTC[C/T]GTTTTGTAAGCTATT	22937
rs376461888	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47415472	CCTGGTGAATATCAC[A/G]TAAGTTTGTAAATTA	22937
rs376469477	snp	A/G/T	5.17731e-05	0.00508766	intron-variant	SCAP	GRCh38.p7	3:47425472	GGCCCAGTGGAGCCT[A/G/T]CTAGGGACCTACCCG	22937
rs376567000	snp	A/G	0.000153988	0.00877327	intron-variant	SCAP	GRCh38.p7	3:47420511	GGGGCCTGGAGCACC[A/G]GCCCTCCAGAAGAGG	22937
rs376594370	snp	A/T			upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47478076	CCCTGGGCCCACTGT[A/T]CCAAAGTCTTCTCTC	22937
rs376600885	in-del	-/G			intron-variant	SCAP	GRCh38.p7	3:47470792	CTTGAACCCAGGGGG[-/G]CGAAGGTTGCAGTGA	22937
rs376602798	snp	C/T	0.000296573	0.0121737	intron-variant	SCAP	GRCh38.p7	3:47414783	ATCAGGCTCCCACCC[C/T]GTGCCGGGCCACTCC	22937
rs376664532	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47421781	TGGCCTGCCAGCCCT[A/G]GGGGAAAGACGGGCG	22937
rs376681326	in-del	-/TATATAT			intron-variant	SCAP	GRCh38.p7	3:47455088	ATATATATATATATA[-/TATATAT]AATCAACTGAAAACC	22937
rs376688862	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47458025	GGGCACGGTGGCTCA[C/T]GCCTGTAATCCCAGA	22937
rs376691294	in-del	-/CATGACAGTGTGCCCAT	0.00597247	0.0543191	intron-variant	SCAP	GRCh38.p7	3:47422907	GTCTGCACGGGCCAG[-/CATGACAGTGTGCCCAT]CAACCACATGGCAGA	22937
rs376691812	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47423389	AGAGAAAATACTAGG[C/T]GCTAAACTCCCCAGA	22937
rs376747557	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47432501	ATCTCCTCAAGGACA[C/G]TGAGCCTCTATCTGT	22937
rs376770796	snp	A/C/G	8.28694e-05	0.00643654	missense, intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47426104	TGGACCAGGCTCTCC[A/C/G]CCCGAAGGCTGCAGT	22937
rs376815165	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47453216	TCTGGTTTGTCTTCC[C/T]ACATGGTCAGCATGG	22937
rs376828685	snp	A/G	1.6591e-05	0.00288015	intron-variant	SCAP	GRCh38.p7	3:47414133	CAAGCTCAGTCCTGA[A/G]TCCTTCCCTAAAATC	22937
rs376828857	snp	C/G	0.000153988	0.00877328	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47425985	CCCTCAGCCTCCCTG[C/G]CATGAACCTACGCGT	22937
rs376867401	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47422968	AGAGGACCTGGCTGC[A/G]TTCTTCCTCAAGCCC	22937
rs376871560	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47457438	CCCTTCAGGAGAAGG[A/G]AATAACTGAATCACC	22937
rs376901858	in-del	-/AT			intron-variant	SCAP	GRCh38.p7	3:47454018	CATATTAACAGAGAT[-/AT]CATCTCTGCCAATGC	22937
rs376908189	snp	A/G	0.000323551	0.012715	missense	SCAP	GRCh38.p7	3:47417567	GGGAGTCCCGAGAGC[A/G]GCCACAGACCGCCCG	22937
rs376956705	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47468885	TTAATCCATCTTGAA[C/T]TGATTTTTGTATAAG	22937
rs376960787	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47460505	CCAGTCCCTCCGTTC[A/G]GGGTCCCTGACTTCC	22937
rs376983008	in-del	-/AAG			intron-variant	SCAP	GRCh38.p7	3:47442437	GACTAGAGAGCAAAG[-/AAG]CAAGTCTCTGAGGTT	22937
rs376992803	snp	A/C	0.000437904	0.0147905	upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47476892	AGGTAAGCCTCCCCT[A/C]AGCCCCTGCCTACTG	22937
rs376995400	snp	A/G	0.00318978	0.0398085	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47425896	CACCAGGTGTGTTCT[A/G]TCTCTCTACCCCAAG	22937
rs376996018	snp	A/G	0.000407947	0.0142761	synonymous-codon	SCAP	GRCh38.p7	3:47418492	CAGCAGCACCAAGAC[A/G]ATGCCGGTGGCCAGG	22937
rs377011536	snp	A/G	0.000215895	0.0103875	intron-variant	SCAP	GRCh38.p7	3:47414663	AACACCTGGGACAGG[A/G]ATGGGCCTCAGGTTC	22937
rs377014914	snp	A/G/T	0.000175498	0.00936609	intron-variant	SCAP	GRCh38.p7	3:47418618	CCCGTCCCCCTCCCC[A/G/T]CACTCTTTCCCACCC	22937
rs377031065	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47447613	GAATTGCTTAAACCC[A/G]GGAGGCGGAGGCCAC	22937
rs377044764	in-del	-/C			intron-variant	SCAP	GRCh38.p7	3:47474149	GGCGCCTGTAGTCCC[-/C]AGCTACTTGGGAGGC	22937
rs377151001	snp	C/T	0.000153988	0.00877328	synonymous-codon	SCAP	GRCh38.p7	3:47418816	CAGGCGGAGCGTGAC[C/T]GGGATGACGGGCAGC	22937
rs377168756	snp	G/T			intron-variant	SCAP	GRCh38.p7	3:47446894	GGCTGCAATGAGCTA[G/T]GACCACACCATTGCA	22937
rs377185576	multinucleotide-polymorphism	CA/GG			intron-variant	SCAP	GRCh38.p7	3:47418875	GGCAGCCTCAGCGGG[CA/GG]GCCTCCCAGGGCTTC	22937
rs377198618	snp	C/T	0.00159617	0.0282053	intron-variant	SCAP	GRCh38.p7	3:47457003	CCAGCCTGGCCAACA[C/T]GGTGAAACCCTGTCT	22937
rs377213743	snp	C/T	5.6215e-05	0.00530135	utr-variant-3-prime, downstream-variant-500B	PTPN23, SCAP	GRCh38.p7	3:47413229	TACATCATCATCATC[C/T]CATGCCCACCTGCCC	22937
rs377329315	snp	C/T	7.6234e-05	0.00617343	missense	SCAP	GRCh38.p7	3:47418230	AGCAGCATGCCGTCG[C/T]TGGCCAGGCACTCGA	22937
rs377388205	snp	C/T	0.00222786	0.0333012	synonymous-codon	SCAP	GRCh38.p7	3:47418369	CTCCGTCTCGGGTGG[C/T]GCATAGCCGTAGTCG	22937
rs377478393	snp	A/T	0.000114397	0.0075621	intron-variant	SCAP	GRCh38.p7	3:47418296	CTCCGGCCCTCCCCT[A/T]CCCGGCCACTGTGCC	22937
rs377497069	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47435924	GCATGGCCATGTGAA[C/T]CTGTGGTCCCAGCTA	22937
rs377500079	snp	C/G/T	3.29915e-05	0.00406138	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47427416	CAATGGGCACCTTTA[C/G/T]AGGTCTGAAGGGAAC	22937
rs377502093	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47433425	CTGCACCAACACTTT[C/G]TATCATCATCCCATC	22937
rs377617775	snp	G/T			intron-variant	SCAP	GRCh38.p7	3:47445834	GCCTGGCCTCCCAAA[G/T]TGCTGGGATTACAGG	22937
rs377670609	snp	A/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47470562	AAGGACAGGAAAGGA[A/T]CCCAAAGAAAAGAAC	22937
rs377731584	snp	A/C/G/T	0.000341784	0.0130685	missense	SCAP	GRCh38.p7	3:47417393	CACTGGGGGCCCAGG[A/C/G/T]GAGGGAAGGGGAGCC	22937
rs386396566	in-del	-/A			intron-variant	SCAP	GRCh38.p7	3:47453401	ATTTTTAATGGAAAA[-/A]AAAAAAGACCTGCTT	22937
rs386396567	in-del	-/A			intron-variant	SCAP	GRCh38.p7	3:47453404	TTTAATGGAAAAAAA[-/A]AAAGACCTGCTTATG	22937
rs386396568	in-del	-/AAT			intron-variant	SCAP	GRCh38.p7	3:47472464	AAATAAAATAAAATA[-/AAT]ATAATAATAATAATA	22937
rs386396569	in-del	-/AAT			intron-variant	SCAP	GRCh38.p7	3:47472479	ATAATAATAATAATA[-/AAT]ATAATTAAATGAAGC	22937
rs386660777	in-del	GGGAAAGA/T			intron-variant	SCAP	GRCh38.p7	3:47421783	GCCTGCCAGCCCTGG[GGGAAAGA/T]CGGGCGAGAAAAGAT	22937
rs386660778	multinucleotide-polymorphism	AG/GC			intron-variant	SCAP	GRCh38.p7	3:47421794	CTGGGGGAAAGACGG[AG/GC]GAGAAAAGATGGCAT	22937
rs386660779	multinucleotide-polymorphism	CAC/GAT			intron-variant	SCAP	GRCh38.p7	3:47439034	CTATTCTAAGCACTT[CAC/GAT]ATGTACAGATACATC	22937
rs386660780	multinucleotide-polymorphism	GA/TT			upstream-variant-2KB, intron-variant, nc-transcript-variant	SCAP, LOC105377073	GRCh38.p7	3:47476283	ACTTGGGCAACGTAG[GA/TT]GACCTCCGTCTCCAC	22937
rs397753214	in-del	-/AAT	0	0	intron-variant	SCAP	GRCh38.p7	3:47472484	AATAATAATAATAAT[-/AAT]TAAATGAAGCTGAAA	22937
rs397940322	in-del	-/T			intron-variant	SCAP	GRCh38.p7	3:47469104	GCAATCCCAGCACTT[-/T]GGGGATGCCAAGGTG	22937
rs397989464	in-del	-/T	0	0	intron-variant	SCAP	GRCh38.p7	3:47432332	TTCCTTTTTCTTTTC[-/T]TTTTTTTTTTTTTTT	22937
rs397989466	in-del	-/T	0	0	intron-variant	SCAP	GRCh38.p7	3:47465853	GCCACTGCACCCAGC[-/T]TTTTTTTTTTTTGTT	22937
rs527255050	snp	C/T	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47441042	GAGTGGCGGGGACTA[C/T]AGGTGCAGGCCACCA	22937
rs527328748	snp	G/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47449088	TTTAAGTATTATTTT[G/T]ATTTTTCCCAAGCAT	22937
rs527476699	snp	C/T	0.00209733	0.0323151	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47425629	GGAGGGCAGAGAGGG[C/T]GTATCAGGGCGGCCC	22937
rs527488110	snp	C/T	0.000144728	0.00850548	missense	SCAP	GRCh38.p7	3:47418406	GGCAGCTCCCCGCGC[C/T]TCCGCCGCCCGGGCC	22937
rs527502511	snp	A/C	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, upstream-variant-2KB	SCAP, LOC105377073	GRCh38.p7	3:47475524	GACGCCGCGCATCTC[A/C]CCCCGTCACACCAGG	22937
rs527518959	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47433139	CACCTGGCTGAGTTA[C/T]ATGAACCAAAAATTC	22937
rs527572368	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47467726	CAAATTGAAATCACA[A/G]TGAGATACCAATTCC	22937
rs527593044	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47419000	AGAGGTAGGTCCCTC[C/T]CCAGCCCAGCTTAGC	22937
rs527609153	snp	A/C	0.000399281	0.0141238	utr-variant-5-prime, intron-variant, upstream-variant-2KB	SCAP, LOC105377073	GRCh38.p7	3:47475867	CGGCAGCAGGGGCGG[A/C]GCGCGGCGTGCGCGC	22937
rs527721420	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47460267	TCAGCTTACGAAGAT[A/G]ACAGGATTAAGAGAT	22937
rs527747059	snp	C/T	0.00189933	0.0307581	missense	SCAP	GRCh38.p7	3:47417507	CGGCCGCCAGCCCCT[C/T]CTCCTGGTACACCCG	22937
rs527775970	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	SCAP, LOC105377073	GRCh38.p7	3:47474360	TCCATTTCAATTTAT[A/G]ACCAAAAGAATAAAT	22937
rs527777997	snp	C/T	0.00159617	0.0282053	intron-variant	SCAP	GRCh38.p7	3:47464864	ACATGATCTTACATG[C/T]AGAAAACCCTAAAGA	22937
rs527817238	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47473596	TGAAGTACCTGTCAG[A/G]GCCGGTAAAACACTG	22937
rs527855056	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47458011	ATTGAAAAAAGGTCG[A/G]GCACGGTGGCTCACG	22937
rs527887770	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47448166	GATTTCTTTCATCAG[C/G]ATTGTATAGTTTTCA	22937
rs527890134	snp	C/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47465713	GCTCAAGGCTGTAGT[C/G]AGCAGTGACTGCGCC	22937
rs527964267	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47448278	ACATGTTCATTGCTA[A/G]TACATTGATTTTTTT	22937
rs528039236	snp	G/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47463842	CTAAGTTTTTTGGTT[G/T]TTTGTTTTATTTTTG	22937
rs528073578	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47435666	GCTGAGATTACAGGC[A/G]TAAGCAACCGTGCCT	22937
rs528074429	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47416532	GAAAGGATAGGAGTA[C/T]ATCACTCCCCACTGT	22937
rs528075771	snp	C/T	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47472398	GAGATTGCGCCACTG[C/T]AGTCCGCAGTCCGGC	22937
rs528090541	snp	C/G	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47462881	CCCTTCCTGCTTCCC[C/G]ATAGGCTTTGTTCCT	22937
rs528093394	snp	C/T	0.0108347	0.0728009	missense	SCAP	GRCh38.p7	3:47418401	CGCAGGGCAGCTCCC[C/T]GCGCCTCCGCCGCCC	22937
rs528110163	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47439097	CGCTGTCGTAAATTG[A/G]AAATATCCTAAGTCA	22937
rs528255799	snp	C/G	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47437862	ACTTATTTCTGTCGG[C/G]TATATTCCTAGGATG	22937
rs528344053	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47446503	TTACTTTTTTTGTTG[C/T]TGTTGTTCTTCAGTT	22937
rs528385584	in-del	-/C	0.00358779	0.0422022	intron-variant	SCAP	GRCh38.p7	3:47443456	CAAACAGGCATTCTT[-/C]CCCCCCCCTCCTCTA	22937
rs528420584	snp	A/C	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47444750	AAAGTGCTGGGATTA[A/C]AGGCACGAACCACCA	22937
rs528504762	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47453874	TAATTTCCCACCTCT[A/G]ATTTTCTCCATTCAG	22937
rs528514121	snp	C/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47443957	TATTCATCCCACAGA[C/G]GTTCCTGCTCCCAAG	22937
rs528600011	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47435786	GGGCGCAGTGGGTTA[C/T]GCCTGTAACCCCAGC	22937
rs528674457	snp	A/G	0.00279162	0.0372561	upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47477992	GACATCACTCTCTCC[A/G]GGTCTGATCCCTTGA	22937
rs528799931	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47421921	CTGAGTGAGGGCACT[C/T]TGCCAAGAGCAGGGT	22937
rs528827729	snp	A/G	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47457076	ACATTCAGAGAAAAA[A/G]GCAAGGGAGCAGTGT	22937
rs528963104	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47447524	GAAACCTCTTCTCTA[C/T]TAAAAATACCAAAAT	22937
rs529089373	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47464676	TGGTGAAAGACTAAA[A/G]GCTTTTCCCCTAAAA	22937
rs529121290	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47439038	TCTAAGCACTTGATA[C/T]GTACAGATACATCTT	22937
rs529129479	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47425439	AGTGCAAGGCTCTCT[A/G]GCCTGAGCCCACCCT	22937
rs529129524	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47468489	ACAAGCATTTTTTCA[C/T]GTGTCTGTTGGCTGC	22937
rs529207223	snp	C/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47437133	ATTTGGCTGTTTCTG[C/G]TTTGAGCTATTAAGA	22937
rs529227353	snp	A/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47423576	TTTTTCTATCTTTTG[A/T]AGACATGGGGTTTCA	22937
rs529239962	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47454184	CATCCTGGCTAACAC[A/G]GTGAAACCCTGTCTC	22937
rs529295066	snp	C/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47436022	CCACTGCACTCCAGC[C/G]TGGGCAACATAAGAC	22937
rs529317195	snp	C/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47445575	ACTTGGTCTCGAACT[C/G]CAACTTTTTTTTTTG	22937
rs529317957	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47457901	AATGGAGCGAGACTC[C/T]GTCTCAAAATAAATA	22937
rs529398318	snp	A/T			intron-variant	SCAP	GRCh38.p7	3:47418626	CCTCCCCGCACTCTT[A/T]CCCACCCCACCCCAC	22937
rs529435448	snp	A/T	0.00119737	0.0244387	intron-variant	SCAP	GRCh38.p7	3:47472485	AATAATAATAATAAT[A/T]AAATGAAGCTGAAAT	22937
rs529455946	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47473508	TGACAAGCTGGGTGA[A/C]CTTGTAAGAACCCAG	22937
rs529464275	snp	A/G	5.02466e-05	0.00501206	intron-variant	SCAP	GRCh38.p7	3:47422544	GCTTAGGCCTGCAGA[A/G]GGCAGCAACAGGGCA	22937
rs529489887	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47416139	CAGCTCTAGGTCAGA[C/T]GGTGCTGCCACCAAC	22937
rs529524786	snp	C/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47463884	TGCTCTGTCACCCAG[C/G]CTGGATACAGTTGTA	22937
rs529528112	snp	A/G	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47421984	GGTCAGGCCAGGCAA[A/G]GCCATGCGTCTGGCG	22937
rs529556888	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47414755	ACTCTTCCAGCCTCT[C/T]CCTGACGAATGCATC	22937
rs529572140	snp	A/G	0.00159617	0.0282053	intron-variant	SCAP	GRCh38.p7	3:47416650	TTTTTTTTTTGAGAC[A/G]GAGTCTCGCTCTGTC	22937
rs529589828	in-del	-/AT			intron-variant	SCAP	GRCh38.p7	3:47455063	ATACAAAAAAATTAC[-/AT]ATATATATATATATA	22937
rs529688082	snp	A/G	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47420424	GGGCAACTCCCCAGA[A/G]CCAGGCTTCCAGGGG	22937
rs529807337	snp	C/T	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47470182	AGCCTTAAGAGAACT[C/T]GTTTTTTACCCCATT	22937
rs529832053	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47447850	CGTCTCTATGAAAAA[C/T]ACAAAATAGCCGGGC	22937
rs529920588	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47461917	CAGGCACCTATAATC[C/T]CAGCTACTTGGGAGG	22937
rs529929507	snp	A/C	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47454722	CACTGCACTCCAGCC[A/C]AGATGACAGAGACTC	22937
rs530040683	snp	G/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47468427	CTAACTGGTGTGAGG[G/T]TATCTCATTGTGGTT	22937
rs530049459	snp	C/T	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47459795	TTAAACAACAGAAAA[C/T]AGGGTTCAAGAGCAG	22937
rs530099494	snp	A/T	0.000798403	0.0199641	intron-variant, utr-variant-3-prime, downstream-variant-500B	PTPN23, SCAP	GRCh38.p7	3:47413721	ATGATATGGTTTTTT[A/T]AAAAAGTTTAATATT	22937
rs530103700	snp	A/G	6.60153e-05	0.00574485	missense	SCAP	GRCh38.p7	3:47419490	GGTGACTCGCCTGGC[A/G]ACGTCTGGTTCTCAG	22937
rs530193939	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47451976	TACTGTTCCATCCTC[C/T]ATTCCCTCTTCTCTT	22937
rs530265197	snp	G/T			intron-variant	SCAP	GRCh38.p7	3:47434085	CACTGACACCATGTA[G/T]AGTTGTGCCACAGAC	22937
rs530274478	snp	G/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47434120	CTTGCCAGATATGCC[G/T]CTATTTCAGCCGCAG	22937
rs530278569	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47443754	TGCCTGCCCAGTACC[C/T]GTCCCCTTCCATAAG	22937
rs530352387	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47426519	CTGGGCTCACTGCAA[A/G]CTCCGCCTCCTGGGT	22937
rs530398964	snp	A/C	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47471418	GCACAAGCTGGAAGA[A/C]CCTGGATACAAACTT	22937
rs530430963	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47443300	CTCTCTCTCTCTCTC[C/T]CTCTCTCTCTCCCTC	22937
rs530455031	snp	C/T	0.0023933	0.0345097	intron-variant	SCAP	GRCh38.p7	3:47473878	CCTAATGACAGTGAC[C/T]GAGGGAACGGGGGAA	22937
rs530490259	snp	A/C	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47462015	CTCCAGCCTGGGCGA[A/C]AGAGTGAGACTCCAT	22937
rs530504164	snp	C/T	0.000156897	0.00885571	intron-variant	SCAP	GRCh38.p7	3:47415223	CCTCTCCCTTAGAGC[C/T]CCAGCCCTGGGGCTG	22937
rs530506050	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47462709	AGTGAGCCAAGATCG[C/T]GCCATTGCACCCCAG	22937
rs530538594	snp	A/T	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47470458	TAAGTGAACATCTGT[A/T]CACAGGAGTTAACAC	22937
rs530599822	snp	A/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47454178	TGAGACCATCCTGGC[A/T]AACACAGTGAAACCC	22937
rs530686513	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47445657	GCTCACTGTAAACTC[C/T]GCCTTCCGGTGGTTC	22937
rs530767973	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47443122	AAAAGCCAGTTAACA[A/G]AGAGTACTTGGCTCT	22937
rs530842802	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47446457	ATTACAGGCGTGAGC[C/T]ACCGTGCCTGGCCCC	22937
rs530851772	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47435297	AGCTGAAACTCAGAA[A/G]TCATCTAGATTAGAA	22937
rs530853496	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47452171	TATTCCCTGGTTTAC[C/T]ATCTGTCCTCTGTCA	22937
rs531116469	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47427082	ATTCAGAACACTCTA[A/C]CCAGAAGAGGGACTA	22937
rs531147006	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47477354	ATGAGGTCAGGAGAT[C/T]GAAACCATCCTGGCT	22937
rs531163870	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47434762	GAATCACTTGAACCC[A/G]GGAGGCGGAGGTTGC	22937
rs531195340	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47421169	GATGAGAGATGCTGG[C/T]TGGTCCTCAGCTCAC	22937
rs531206733	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47422028	CCAGGGCCAAGGGAG[A/G]AGACCGGAGGAAGGG	22937
rs531233200	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47420486	TCTAAGGCCAAGTGC[A/G]GCACCACAAGGGGCC	22937
rs531301703	snp	C/T	0.00119737	0.0244387	utr-variant-5-prime, upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47475919	GTGGCGCCCTCCCTC[C/T]CTCTCCTGGCCGCCG	22937
rs531405498	snp	C/T	0.00159617	0.0282053	utr-variant-3-prime, downstream-variant-500B	PTPN23, SCAP	GRCh38.p7	3:47413319	CCCTGCCTGGCCCAG[C/T]CTGCACCCCTGTGGG	22937
rs531414132	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47467790	TACAGGTTTGTTACA[C/T]ATGCATACATGTGCC	22937
rs531506173	snp	C/G	0.00199481	0.0315187	intron-variant	SCAP	GRCh38.p7	3:47468569	TTGATAGGGTTGTTT[C/G]ATTTTTTTCTTGTAA	22937
rs531518140	in-del	-/AACTT	0.00119737	0.0244387	downstream-variant-500B	PTPN23, SCAP	GRCh38.p7	3:47413487	AGTAGCACTGCCAGG[-/AACTT]AACTTAACTTACTTA	22937
rs531531524	snp	A/G	1.84032e-05	0.00303335	synonymous-codon	SCAP	GRCh38.p7	3:47419696	GCCAATCCAGACAAC[A/G]GTGCCAGCCTGCAGT	22937
rs531606363	snp	A/C/T	0.000339764	0.0130302	synonymous-codon	SCAP	GRCh38.p7	3:47417577	AGAGCGGCCACAGAC[A/C/T]GCCCGGTGCCGGGGC	22937
rs531701348	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	SCAP, LOC105377073	GRCh38.p7	3:47475223	AGTCCGGAGCCAGGG[C/T]TCCCTGCAACTAACG	22937
rs531709125	snp	A/C	0.0039912	0.0444935	intron-variant	SCAP	GRCh38.p7	3:47465845	GTTTAAAAAAACAAA[A/C]AAAAAAAAGCTGGGT	22937
rs531712786	snp	A/G			upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47476844	TTTGATCATGCTACT[A/G]CATGCCCTTGCTGTA	22937
rs531767652	snp	C/T	0.00914312	0.0669923	intron-variant	SCAP	GRCh38.p7	3:47449183	CCTTTGGTATGCTGT[C/T]TAGGGTCAGATGCAC	22937
rs531774750	snp	A/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47424278	CCAGCAGCCATCCTG[A/T]CTCTAGCCATCCAGC	22937
rs531786044	in-del	-/A			intron-variant	SCAP	GRCh38.p7	3:47437575	TGAAACGCCATCCCT[-/A]AAAAAAAAAAAAATA	22937
rs531820517	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47458149	AAAAATTAGCAGGGC[A/G]TGGCCAGGCGCAGTG	22937
rs531822651	snp	A/C	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47466597	AACTGGATAGTTACA[A/C]GCAAAAGTGAAGTTG	22937
rs531845963	snp	C/G/T	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47418299	CGGCCCTCCCCTACC[C/G/T]GGCCACTGTGCCCCT	22937
rs531928949	snp	C/G	0.00119737	0.0244387	intron-variant	SCAP	GRCh38.p7	3:47457070	AAAGAAACATTCAGA[C/G]AAAAAAGCAAGGGAG	22937
rs531968147	snp	A/T	8.29786e-05	0.00644068	intron-variant	SCAP	GRCh38.p7	3:47414145	TGAGTCCTTCCCTAA[A/T]ATCCCAAGAATCCTA	22937
rs531985127	snp	A/T	0.00199481	0.0315187	intron-variant	SCAP	GRCh38.p7	3:47458982	GGCTAATTTTTTATT[A/T]TCAGTAGAGATGGGG	22937
rs532008052	snp	A/G	0.0023933	0.0345097	intron-variant	SCAP	GRCh38.p7	3:47443807	CAGGGGAACCACCTC[A/G]CTCCACAGGATTTAA	22937
rs532044899	snp	C/T	5.03081e-05	0.00501513	intron-variant, utr-variant-3-prime, downstream-variant-500B	PTPN23, SCAP	GRCh38.p7	3:47413851	GGCAAGGAGGCCCTG[C/T]GCTCAGTCCAGCTTC	22937
rs532049523	snp	C/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47450457	CACAAAAGGAGAATA[C/G]AGGGAAACGTTAGTA	22937
rs532083434	snp	A/C	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47419824	ATGGAGAGAGGACAC[A/C]GGCCCCACTGCGTCC	22937
rs532108553	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47415789	AGGCAATGCATGTCT[A/G]CCTACAACCTCTGCC	22937
rs532126223	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47426399	CTTTGTCTCCCTTTC[C/T]GGACCTACTCCAACA	22937
rs532154503	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47414471	CCCCAGTGGGTGGGG[C/T]CCTGACTGCTTCCTG	22937
rs532243632	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47439742	TTTCATCAGATTTTC[C/G]CAGAGGAAAGAACAG	22937
rs532270743	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47476376	TGAGGTAGGAGGATC[A/T]CCTGAGCCCGGGAGG	22937
rs532381649	in-del	-/ACACACACAC	0.217851	0.247924	intron-variant	SCAP	GRCh38.p7	3:47443234	CCTCAATCCCAAAAT[-/ACACACACAC]ACACACACACACACA	22937
rs532382652	snp	A/G	0.0023933	0.0345097	utr-variant-5-prime, intron-variant, upstream-variant-2KB	SCAP, LOC105377073	GRCh38.p7	3:47475851	GCGGCGGCGACGGGG[A/G]CGGCAGCAGGGGCGG	22937
rs532510592	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47467645	AAACAACAACAAAAA[A/G]GAAGATATACAAATG	22937
rs532521279	in-del	-/AG	0.00119737	0.0244387	intron-variant	SCAP	GRCh38.p7	3:47460905	TTCCAAACAGTGCAA[-/AG]AGGGGAGGAGTTTGT	22937
rs532628359	snp	G/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47449242	AGTTCATATGCAACT[G/T]TATGAGTTCAATTTG	22937
rs532696783	snp	A/G	3.4042e-05	0.00412551	synonymous-codon	SCAP	GRCh38.p7	3:47414944	ACAGGCCACTGTGTC[A/G]CTGCTGCTGTACACT	22937
rs532704912	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47442261	AAACTCCTCCTTTAC[A/G]ACGTCATTGTCAGCC	22937
rs532804164	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47457918	TCTCAAAATAAATAA[A/G]TAAAAAGAAAATTGC	22937
rs532868749	snp	A/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47442817	TGGTTAGGGTTAGAA[A/T]ACCTACTGTCCTAAG	22937
rs532898589	snp	A/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47440120	GCTGTTAGATCTGAA[A/T]AGGGAAATTAAGTGC	22937
rs532977246	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47472740	CTGGCTTCCTCCCAC[C/T]ACCCCTACCACCTTC	22937
rs533012063	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47434581	GGTGGCTCACGCCTG[C/T]AATCCCAGCACTTTG	22937
rs533055979	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	SCAP, LOC105377073	GRCh38.p7	3:47475268	TAAGCCGGTTAAATA[C/T]TGAGGTCATAAACCC	22937
rs533144953	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47432294	TGCACTCCAGCCTAG[C/T]GAAAGCAAGACTCCG	22937
rs533154393	snp	C/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47424351	GCCACTGCTAGACCA[C/G]ACTTCTGCTGGCCCT	22937
rs533166948	snp	C/G	0.00119737	0.0244387	intron-variant	SCAP	GRCh38.p7	3:47429354	TGTAGGCCAAATCAG[C/G]GCCCATGCCTGTTTT	22937
rs533178482	snp	C/T	0.00398564	0.0444627	intron-variant	SCAP	GRCh38.p7	3:47440964	TAGAGTGCAGTGGCG[C/T]GATCTCAGCTCACTG	22937
rs533186051	snp	C/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47428888	TGAGATAAAAGAACT[C/G]GCTGAAATAAGCTGG	22937
rs533202784	snp	A/G	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47437793	TTAATTAAAAAAAAG[A/G]AAAAAAAAGAATAAA	22937
rs533217629	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47423154	AATGGACGGCTGCCT[A/G]CAGCCCCATTCCTCA	22937
rs533263316	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47468859	TGGTTTTAGGTCTAA[C/G]ATTTAAGTCTTTAAT	22937
rs533270902	snp	C/T	0.000837248	0.0204432	synonymous-codon	SCAP	GRCh38.p7	3:47417697	AGGCGGCGGAGGGCC[C/T]CGGGGGCGGTGTCTC	22937
rs533325729	snp	C/T	0.00119737	0.0244387	intron-variant	SCAP	GRCh38.p7	3:47469204	AATACAAAAATTAGC[C/T]GGGTGTGGTGGCACA	22937
rs533336925	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47464789	ACTGCCTCATTTACC[C/T]TTTCTCTCCAGGCAT	22937
rs533360421	snp	A/G	0.00159617	0.0282053	intron-variant	SCAP	GRCh38.p7	3:47460724	CACTGTGCCCAGCTA[A/G]TTTTCTTATTTTTAG	22937
rs533422842	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47457201	CAGCCTCTGGGGAGA[A/G]GATCTGGTAGCCAGG	22937
rs533423990	snp	A/G	0.00159617	0.0282053	intron-variant	SCAP	GRCh38.p7	3:47472043	TACTCGGGAGGCTGA[A/G]GCAGGAGACCAAGAT	22937
rs533429168	snp	A/C	0.00438332	0.0466095	intron-variant	SCAP	GRCh38.p7	3:47416749	CTCCTGCCTCAGCCT[A/C]CCAAGTAGCTGGGAC	22937
rs533466209	snp	A/C	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47472654	TTAAGCAGAAACTGT[A/C]AAATGGCAGTGGTCA	22937
rs533469634	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47423429	ACCACCAAACACAAG[A/C]CCCACCCACACTGAA	22937
rs533548698	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47449197	TTTAGGGTCAGATGC[A/C]CGTATGTTAGTTCTG	22937
rs533601190	snp	A/G	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47430813	CCAGCTGAGGGATGA[A/G]GGGCTGTCTCCACGC	22937
rs533682365	snp	C/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47474050	GCGGACGGATCATGA[C/G]GTCAGGAGATAGAGA	22937
rs533730649	snp	C/T	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47450827	AAATCTCAGTATCTT[C/T]ACATTTTTCACTATA	22937
rs533755340	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47466090	GTGAGCCAAGATTGC[A/G]TCACTGCACTCCAGC	22937
rs533875400	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47458343	CTGAGGCAGGAGAAT[C/T]GCTTGAACCCTGGAG	22937
rs533907010	snp	A/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47424488	GAAGGCCCACTCACC[A/T]TTGTTGAGAAGCTGT	22937
rs533929812	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47416825	TAGAGACGGGGTTTC[A/G]CCGTTTTAGCCGGGA	22937
rs533965368	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47416364	AGGAGGCCAAGCACG[A/G]CAGAGGCAGGGAGAG	22937
rs534018496	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47437859	AGCACTTATTTCTGT[C/T]GGGTATATTCCTAGG	22937
rs534032004	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47456771	GTCTGGGCAACAAAG[C/T]GAGACTCCGTCTCAA	22937
rs534062046	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47464102	CTCACTGCAACCTCC[A/G]CCTCCCAGGTTCAAG	22937
rs534089399	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47459399	ATGTGACGAGTCTCG[C/T]TGCGTTACTACTTCA	22937
rs534097091	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47438534	AAAAGTTAATTTAGG[C/T]TGGGCACGGTGGCTC	22937
rs534097234	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47447667	GCACTCCAGCCTGGG[C/T]AATACAGCGAGACTC	22937
rs534167075	in-del	-/CG	0.437542	0.165312	intron-variant	SCAP	GRCh38.p7	3:47417890	AGAGGGGGCGGGGGA[-/CG]GGGGTGAGAGGGGGC	22937
rs534201169	snp	A/C	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47472830	TCACGCCTGTAATCC[A/C]AGCACTTTGGGAGGC	22937
rs534204318	snp	G/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47439241	TGGTGAAACCCCGTC[G/T]CTACTAAAAATACAA	22937
rs534231902	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47422671	GCCATTCCACCAAAG[C/T]ACCCCAACCCTCAGG	22937
rs534243795	in-del	-/TG	0.00119737	0.0244387	intron-variant	SCAP	GRCh38.p7	3:47462812	TACTTATTTCCTAGT[-/TG]TGAGTGACATCATGT	22937
rs534294591	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47455715	GAAAAGTCAATATAA[C/T]GTAACCAAAGTGTCA	22937
rs534331608	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47454227	AAAAAATTAGCCGGG[C/T]GAGGTGGCGGGCACC	22937
rs534347159	snp	A/G			upstream-variant-2KB, utr-variant-5-prime, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47475983	TTACCCTCCCGCCCC[A/G]CCGCCCTCCGCACGT	22937
rs534387966	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47428402	CTCCATCCTTCTTGC[C/T]TGTTCTATCTCTGCA	22937
rs534395053	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47469831	TACCCTGGGCAGTTG[A/G]CAAGACTCCATTTTG	22937
rs534422829	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47431827	CACAGTCACACTGTC[C/T]TCTTTGGAAGAAAGT	22937
rs534479396	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47428993	CATACTAACTCCCCC[C/T]GGAATTTGCACATGG	22937
rs534508838	snp	A/G	0.00279162	0.0372561	intron-variant	SCAP	GRCh38.p7	3:47445939	GGAGTGCGGTGGTGC[A/G]ATCTCAGCTCACTGC	22937
rs534572987	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47445214	ACATTCTAACATTCC[C/T]GTATTTGTTTGAATA	22937
rs534605084	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47470941	CCCAAAGTAACACCT[A/G]TCAATTAATAAACTT	22937
rs534631373	snp	G/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47422042	GGAGACCGGAGGAAG[G/T]GTCTAGGAACCCCAC	22937
rs534670160	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47434879	TATATGGTACACTGA[C/T]AAAGCTGTTAAAGTA	22937
rs534692012	snp	C/T	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47445830	GCCAGCCTGGCCTCC[C/T]AAAGTGCTGGGATTA	22937
rs534749349	snp	C/T	0.00199481	0.0315187	intron-variant	SCAP	GRCh38.p7	3:47469075	AAAATGGGCCAGGCA[C/T]GTTGGCTCACACCTG	22937
rs534749407	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47477446	CGTGGTGGCAGGTGC[C/T]TGTAGTCCCAGCTAC	22937
rs534828508	snp	A/C	1.64765e-05	0.00287019	intron-variant, missense, upstream-variant-2KB, utr-variant-5-prime	SCAP	GRCh38.p7	3:47427230	TGTAGAGGCTCACCC[A/C]GCTGTACTTCCCAGG	22937
rs534867675	snp	A/C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47428311	AAGGCTATGTGTGTG[A/C/T]CATCTGCATAGGTCC	22937
rs534868683	snp	A/C	0.00159617	0.0282053	intron-variant	SCAP	GRCh38.p7	3:47472055	TGAGGCAGGAGACCA[A/C]GATTGCAGTAAACCA	22937
rs534875945	in-del	-/T			intron-variant	SCAP	GRCh38.p7	3:47466929	TATCTTAAAAAAAAA[-/T]AAATACAAAAAAAAT	22937
rs534904141	snp	C/G/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47469717	ACCATGTAAGACATG[C/G/T]CTTTGCTCCTCTTTC	22937
rs534976458	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47426731	GTGAGCCACCGCGCC[C/T]GGCCTCCAACACTCT	22937
rs534997037	snp	A/T	0.00159617	0.0282053	intron-variant	SCAP	GRCh38.p7	3:47462218	CCACCATCCATCTTT[A/T]TTATCTTCCTAAACT	22937
rs535002338	in-del	-/T	0.0310518	0.120672	intron-variant	SCAP	GRCh38.p7	3:47445910	GAGACAGAGTCTTGC[-/T]CTGTCACCAGGCTGG	22937
rs535065907	snp	C/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47434358	AGGTACACAGATGAG[C/G]TAGTCAAGCTTCAAT	22937
rs535148116	snp	C/T	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47446022	CTGGAATTACAGATG[C/T]GCGCCACCACGCCCA	22937
rs535264774	snp	C/T	3.31713e-05	0.00407242	intron-variant	SCAP	GRCh38.p7	3:47414115	CTGGAGGCAAGGACA[C/T]GACAAGCTCAGTCCT	22937
rs535324973	snp	C/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47453341	TGAGCCCAGAAGTTC[C/G]AGACCAGTCTGGGCA	22937
rs535340958	snp	C/T	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47415316	GAAAGCACATGGTGC[C/T]AGAACAGATGCTGGA	22937
rs535408255	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47416862	CGATCTCCTGACCTC[A/G]TGATCCGCCCGCCTC	22937
rs535416538	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47428075	GCAGCTTGCCAATTA[C/T]ACACATTGTATGCCA	22937
rs535441382	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47430437	AGTTATGGCCCAGGA[A/G]AAGCTGAGTAGAGCC	22937
rs535526095	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47437944	AACAGTTTTCCATAG[C/T]GGTTGTACAAATTTA	22937
rs535548821	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47470645	AGGCAGGCAGATCAC[C/T]GGAGGTCAGGAGTTC	22937
rs535560223	snp	C/T	0.00159617	0.0282053	intron-variant	SCAP	GRCh38.p7	3:47429025	ACCTGTGAGGTGGCA[C/T]CAAGAGATAACTGGG	22937
rs535587728	snp	A/C	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47469884	CAGATTGGAACAAGA[A/C]ATTAGCCACAGATTC	22937
rs535600103	snp	C/G/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47421318	GGGGACTGAAGGCCT[C/G/T]ATCCAACCCGGAAAC	22937
rs535609295	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47478177	CTGTCATTCTCCTCA[C/T]TCACCACCTCTTCCC	22937
rs535622156	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47463127	ACAGTAGCTGTTCTT[C/T]CCCAGCCATCTCAGT	22937
rs535642033	snp	A/G	0.00119737	0.0244387	intron-variant	SCAP	GRCh38.p7	3:47420361	GCTGCTTCTCCCACA[A/G]GCTTATCTCCTCAGA	22937
rs535660784	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47462296	TTACTATATAACTTG[C/T]CAAAGGTTTTTCTGT	22937
rs535695319	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47429577	TGGTCTCGAACTCCT[A/G]GGCTCAAGTGATCCT	22937
rs535719047	snp	G/T			intron-variant	SCAP	GRCh38.p7	3:47459107	ACCGTACCCAGCCAA[G/T]AATCTGTTTTAAAGC	22937
rs535755630	snp	A/G	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47455367	TGGGAGGCCGAGATG[A/G]GCAGATCACCTGAAG	22937
rs535759308	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47416543	AGTATATCACTCCCC[A/G]CTGTCACTGCTTAAG	22937
rs535759382	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47461793	AATCCTAGGACTCTC[C/G]GAGGCCGAGGCAAAC	22937
rs535802209	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47420833	CTGCTCGCACAGGAC[C/T]GCTGTCCTGCCCGAG	22937
rs535969450	snp	A/G	3.38541e-05	0.00411411	synonymous-codon	SCAP	GRCh38.p7	3:47414872	CAAGCGCCCAGCAGC[A/G]GCTTTCAGGGCTGTG	22937
rs536010802	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47434467	ATTTATATCAGTGTT[C/T]GGCCCAGAGACAGTC	22937
rs536015854	snp	C/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47454293	AATGGTGTGAACCCC[C/G]GGGGACGGAGCCTGC	22937
rs536063639	snp	C/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47453007	AGCCTGAGTGGGAAG[C/G]ACTGCTTGAGCCCAG	22937
rs536125750	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, missense	SCAP	GRCh38.p7	3:47435087	TCCTTCACAGGGGTG[A/G]TGAATTCCACAGGTC	22937
rs536128256	snp	A/C	0.00478085	0.0486577	intron-variant	SCAP	GRCh38.p7	3:47445328	CTCCACTCAATGCAA[A/C]CTCTGCCTCCCAGAT	22937
rs536260046	snp	A/G	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47460122	TCAGACCTTATGGTT[A/G]TCTTCCCTTGTTCCC	22937
rs536384756	snp	C/T	0.00119737	0.0244387	intron-variant	SCAP	GRCh38.p7	3:47460756	AGATATGGGGTTTCA[C/T]CATCCTGGCCAGGCT	22937
rs536437953	in-del	-/TAAGA	0.00119737	0.0244387	intron-variant	SCAP	GRCh38.p7	3:47454069	CAACCCTCATCCTTT[-/TAAGA]TAAGAATAGACAGGC	22937
rs536493477	snp	A/G	0.00119737	0.0244387	intron-variant	SCAP	GRCh38.p7	3:47425098	TCTCACACCTCCAGT[A/G]GCTTAAGCCATCAAG	22937
rs536540265	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47476518	ATGCAGATGAGAAGA[A/T]TAAATAATGTCCATA	22937
rs536750660	snp	A/C	0.0123036	0.0774623	intron-variant	SCAP	GRCh38.p7	3:47466146	AAAACCAAAAAAAAA[A/C]AAAAAAAAAAAGAAA	22937
rs536798068	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47436325	AAGGAAAAGCCCTGA[C/T]CTTTCATCAAAAAGT	22937
rs536887963	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47445116	CATCAAATGGGTATG[C/T]CACATTTTGTTTGTC	22937
rs536912199	snp	A/G	0.00119737	0.0244387	utr-variant-5-prime, intron-variant, upstream-variant-2KB	SCAP, LOC105377073	GRCh38.p7	3:47475854	GCGGCGACGGGGGCG[A/G]CAGCAGGGGCGGAGC	22937
rs536946341	snp	A/G			upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47477160	CCACACTATTGTCAC[A/G]ATGAAAGTAACAATG	22937
rs536948402	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47437359	CAGGAAAATCACTTG[A/C]ACCGGTGAGCTGAGA	22937
rs537008880	snp	A/C	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47453199	TGCATTTGCACTTCA[A/C]TTCTGGTTTGTCTTC	22937
rs537022912	snp	A/G			intron-variant, upstream-variant-2KB	SCAP, LOC105377073	GRCh38.p7	3:47475036	TATGGCCGCTTCACG[A/G]TAAGTATTACAAAAT	22937
rs537037593	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47427908	TCAGCTCTGAGGACG[C/G]GCAAGTGTACTATAA	22937
rs537045026	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47452481	GATACAAAGCACCTC[A/G]GGCATTCTGGAAGAA	22937
rs537108959	in-del	-/A	0.0111196	0.0737302	intron-variant	SCAP	GRCh38.p7	3:47469184	AAACCCTATCTCTAC[-/A]AAAAAATACAAAAAT	22937
rs537127810	snp	C/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47444256	TGTTTTCTTCGGTCT[C/G]TGCTAGAGGGAACCT	22937
rs537166284	snp	C/G	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47434216	ACTGTCAGAGAGAAG[C/G]GGGAGGAGAGCTCTG	22937
rs537294866	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47478302	CAAGCACCTAGCTAA[C/G]TACCTTTGTGCCTTG	22937
rs537308511	snp	A/G	1.66026e-05	0.00288115	missense	SCAP	GRCh38.p7	3:47414633	GTGAAGAGGCAGCAC[A/G]AGTCCTCCAGACGGA	22937
rs537341622	snp	A/C	0.00119737	0.0244387	intron-variant	SCAP	GRCh38.p7	3:47469463	ACCTCTGGGTCCAAA[A/C]AATTCTTCCTCAGCT	22937
rs537409255	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47433607	CACAATGGCTCACGC[C/T]TGTAATCCCAGCACT	22937
rs537438108	snp	C/G	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47424876	AGGCGGGCCTAGCCA[C/G]AGCCAAGATCAAAGC	22937
rs537465392	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	SCAP, LOC105377073	GRCh38.p7	3:47474997	ATAAAAGAAACACAC[A/G]CAACGCTAACATTAA	22937
rs537474874	snp	A/C	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47424573	CTGTCCCACACTCCC[A/C]GCAGCAAACCCTAAG	22937
rs537586102	snp	A/G	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47466150	CCAAAAAAAAAAAAA[A/G]AAAAAAAGAAAGAAA	22937
rs537629305	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47419979	AGGTTTGACACAGAA[C/T]GTCCCCACCCCTAAG	22937
rs537652301	snp	A/C	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47459444	CACCCCCAATATTTC[A/C]ACATAGGTTCTTTCT	22937
rs537667976	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47426638	GAGACGGGGTTTCAC[C/T]GTGTTAGCCAGGATG	22937
rs537893931	snp	C/T	0.00835141	0.0640778	intron-variant	SCAP	GRCh38.p7	3:47459021	TGTTGGTCAGGCTGG[C/T]TTCAAACTCCTGACC	22937
rs537932521	snp	A/G	0.00358779	0.0422022	intron-variant	SCAP	GRCh38.p7	3:47447710	AAAAAGAAAAGAAAA[A/G]AAAAAAGAAAAAAAG	22937
rs537980838	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, upstream-variant-2KB	SCAP, LOC105377073	GRCh38.p7	3:47475585	CTCCAGGGGCCGGCC[G/T]GTGCAGGGACACGGC	22937
rs538004742	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47431004	ACAACCAGAGGCAAC[C/T]GTCTGAGCCTTTGTG	22937
rs538038057	snp	A/T			intron-variant	SCAP	GRCh38.p7	3:47458342	GCTGAGGCAGGAGAA[A/T]CGCTTGAACCCTGGA	22937
rs538098822	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47439403	GACAGAGTGAGACCC[C/T]GTCTCAAAATCAAAA	22937
rs538169049	in-del	-/G	0.000116119	0.00761879	intron-variant	SCAP	GRCh38.p7	3:47421053	AGAGCACATGGGGAT[-/G]GGGGGGTGCCGTGAC	22937
rs538238778	snp	A/C	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47419236	GTTTTAATTATTTGC[A/C]TAATTCAAACCTGTG	22937
rs538246428	snp	A/G	0.00199481	0.0315187	intron-variant	SCAP	GRCh38.p7	3:47456851	CTGACAAGGTGCTAA[A/G]TTCCCGCGTATATAA	22937
rs538250696	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47464933	TTGTAGGATGCAAAA[C/T]GAACATGCAAAAATC	22937
rs538272629	snp	A/G	1.7904e-05	0.00299193	intron-variant	SCAP	GRCh38.p7	3:47417279	GCGGACAGCCGCTCT[A/G]CCCACCTTTAGCCCC	22937
rs538275805	snp	G/T	6.05199e-05	0.00550057	intron-variant	SCAP	GRCh38.p7	3:47418538	CTGCACGGGAGGGCG[G/T]ACTGCTGTGAGACAC	22937
rs538284514	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47425676	CCCACTGGGGCTCCC[A/G]GGAGTAGGTTGCCCT	22937
rs538327176	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47436129	TTGCCAAATTAGATA[C/T]AAGGGAACAATAAAA	22937
rs538420931	snp	C/T	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47452341	CCAGCCTGGGCAACA[C/T]AGTGAGACCCTGTCT	22937
rs538530597	snp	C/T	0.00318978	0.0398085	intron-variant	SCAP	GRCh38.p7	3:47443316	CTCTCTCTCTCCCTC[C/T]CCGCCCAACTCCCTC	22937
rs538724938	snp	A/G	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47460023	GGAAAAGAATTTAGC[A/G]ATATCTTCCCTACTT	22937
rs538742387	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47440718	TACTAAAAATACAAA[A/G]AATTAGTGGTGCACG	22937
rs538753006	snp	C/T	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47467887	CCCCTCCCCCCATCC[C/T]CCGGCAGGCCCTGGT	22937
rs538801823	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47424650	CTCTGCTTTGGAGCC[A/G]AAGGAAGGGAGGGCC	22937
rs538909412	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47431860	TCATGCATAGTCCAC[A/G]CTTTAGGATACATTA	22937
rs539014752	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47429660	AGAGATGGGGTCTCA[C/T]TATGTTGCCCAGGCT	22937
rs539036307	snp	A/G	0.00119737	0.0244387	intron-variant	SCAP	GRCh38.p7	3:47458209	AGGCCAAGGCGGGTG[A/G]ATCACGAGGTCAGGA	22937
rs539047580	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47447835	AACACAGTGAAACCC[C/T]GTCTCTATGAAAAAT	22937
rs539075971	in-del	-/C	0.0027972	0.0372931	intron-variant	SCAP	GRCh38.p7	3:47465845	TTTAAAAAAACAAAA[-/C]AAAAAAAAGCTGGGT	22937
rs539176068	snp	A/C	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47432757	ATCATGGCTCACTGC[A/C]GCCTTAAACTCCTGG	22937
rs539214699	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47432784	CTGGGCTCAAGCGAT[C/T]CTCCTGCCTCAGTAC	22937
rs539275305	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47441180	GCTGGGATTACAGCC[A/G]TGAGCCACCACGCCC	22937
rs539290693	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	SCAP, LOC105377073	GRCh38.p7	3:47475668	CAGGGCCGGCCCGCA[C/T]GGCTGCTGGACAGCG	22937
rs539334942	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47425036	TGACCTATTTCATTA[A/G]GCATTTAAATGTTCT	22937
rs539404239	in-del	-/A			intron-variant	SCAP	GRCh38.p7	3:47462033	GTGAGACTCCATCTC[-/A]AAAAAAAAGCAATCT	22937
rs539471980	snp	C/T	0.00119737	0.0244387	intron-variant	SCAP	GRCh38.p7	3:47473072	GCAAGAAGAGCGAAA[C/T]TCCATCTCAAAAAAA	22937
rs539478937	snp	C/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47421415	TCACCAACCCAGCTA[C/G]AGCCCAGGCCTGATT	22937
rs539532397	snp	A/C	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47430798	GGGGCAGGGCCCAGC[A/C]CAGCTGAGGGATGAG	22937
rs539556999	snp	G/T	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47422914	CGGGCCAGCATGACA[G/T]TGTGCCCATCAACCA	22937
rs539584771	snp	A/G	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47471928	GGTGGATCACTTGAG[A/G]CCAGGAGTTTGAGAC	22937
rs539607484	snp	A/C	0.00159617	0.0282053	intron-variant	SCAP	GRCh38.p7	3:47446118	TGACCTCGTGATCTG[A/C]CCGCCTCAGCCTCCC	22937
rs539609108	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47456674	GGAGGCTGAGACAGG[A/G]GAATCACTTGAACCT	22937
rs539630327	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47465412	TTCTTTAAATGACAA[C/T]GTTATCCAAAGCTAT	22937
rs539636426	snp	C/T	1.8795e-05	0.00306548	synonymous-codon	SCAP	GRCh38.p7	3:47417307	CCCTCTGCCCACCTC[C/T]AGCCGGCCGCTGCTC	22937
rs539645139	snp	C/T	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47455451	AATACAAAAATTAGC[C/T]GGGCATTGTGGCACG	22937
rs539662238	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47452677	CTCTATTTAACACAC[A/C]CTCCAGCTGACAGTG	22937
rs539672329	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47416926	CCACCGCGCCCGGCC[A/G]CCCCTAACGCTTTTA	22937
rs539682526	snp	C/T			intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47426725	ACAGGCGTGAGCCAC[C/T]GCGCCCGGCCTCCAA	22937
rs539708363	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47465994	AAAAATTAGCTGGGC[A/G]TGGTGGCAGGTGCCT	22937
rs539715562	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47421408	TCATGCATCACCAAC[C/T]CAGCTAGAGCCCAGG	22937
rs539744131	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47457629	ATTACTTCTCTGGGC[C/T]GGGCACGGTGGCTCA	22937
rs539862194	snp	C/G	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47463864	TTATTTTTGAGATAG[C/G]GTCTTGCTCTGTCAC	22937
rs539864836	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47478957	TTTGTATTTTTAGTA[A/G]AGACGAGGTTTTTGC	22937
rs539896590	snp	A/T	0.00119737	0.0244387	intron-variant	SCAP	GRCh38.p7	3:47465169	TGGAAGATGATATTC[A/T]TTTTTTTTTTTCTTT	22937
rs539947950	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47462388	TGTGTAGTAAAGGCA[C/T]ACGCAGTGAAGCCTC	22937
rs540197029	snp	A/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47416980	GACTGCCCTCTGCTC[A/T]CAGGTGTGGAGCTGG	22937
rs540359770	snp	C/T	0.00119737	0.0244387	intron-variant	SCAP	GRCh38.p7	3:47445530	GATTACAGGCATGAG[C/T]CACCACGCCAGGCCA	22937
rs540441420	snp	G/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47429268	CACATTGGGCAGCGA[G/T]CCTCTTTTGCTCAAT	22937
rs540442006	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47457674	GCACTTTGGGAGGCC[A/G]AGGTGGGTGGGTCAC	22937
rs540481232	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47472431	GGGCGACAGAGCGAG[A/G]CTCCGTCTCAAAAAA	22937
rs540546282	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47472291	ACAAAAAAATTAGCC[A/G]GGCGCGGTGGCGGGC	22937
rs540565523	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47446931	CCTGGGCAACAGAGC[A/G]AGACTGTGTCAAAAA	22937
rs540775289	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47434168	GTTACCTGACTACTA[C/T]GTTAACCAAAAAGGA	22937
rs540785252	snp	C/T	1.75188e-05	0.00295958	intron-variant	SCAP	GRCh38.p7	3:47415047	CAATGGGTAGACGGC[C/T]CCTGCCCGTCCCACC	22937
rs540829159	snp	C/T	4.94336e-05	0.00497135	intron-variant, missense, utr-variant-5-prime	SCAP	GRCh38.p7	3:47428576	CGGGACAAAGGTGAA[C/T]GAAATACATCTACTG	22937
rs540902852	snp	A/C	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47429999	TATGGCCTTGAAAAC[A/C]CTTTTGACATCTCTG	22937
rs540923600	snp	A/C	0.00159617	0.0282053	intron-variant	SCAP	GRCh38.p7	3:47462532	CATAAAGACACTATG[A/C]TGAAATGAGAAACGC	22937
rs541002044	snp	C/T	0.00119737	0.0244387	intron-variant	SCAP	GRCh38.p7	3:47435346	GTCACATAAACCTTA[C/T]GAAGAAGCCCAACTG	22937
rs541094371	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47477602	AAAAAAAGAAAGAAA[G/T]AATTTTTTAGGTTAT	22937
rs541173752	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47477272	GATCCTATAAAGAAA[A/G]TATTCGCTGGGCGCG	22937
rs541206569	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47478383	TGTGGAGCCTCTGGG[A/G]AAGCTGGGGTTTATG	22937
rs541206919	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47470136	TATTTTCAGATTAAG[C/T]TGGTCAGCTTACAAC	22937
rs541242768	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47468767	TGTTGCCATTGCTTT[C/T]GGTGTTTTAGTCATG	22937
rs541277086	snp	A/T	0	0	intron-variant	SCAP	GRCh38.p7	3:47453980	AACATGTAAGTACTA[A/T]TGTTAAAACAATGTT	22937
rs541284038	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47460065	TATAGGCTCTCTGCA[A/G]GAAGAAAAATATGGC	22937
rs541359848	snp	C/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47461909	CATGGTGACAGGCAC[C/G]TATAATCCCAGCTAC	22937
rs541369635	snp	C/T			missense	SCAP	GRCh38.p7	3:47418668	ACTTGTACAGCGTGA[C/T]GTCTCCATGGGCCTG	22937
rs541381250	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47471070	GTACACAAGGGCTTA[C/T]TGCTCTCTATTTGGA	22937
rs541393380	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47452617	AATTATTGGGCCTAT[C/T]CCAGACCTGGTGAAT	22937
rs541446143	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47439161	TGCCTATAATCCCAG[C/G]ACTTTGGGAGGCTGA	22937
rs541555777	snp	C/G	0.00438332	0.0466095	intron-variant	SCAP	GRCh38.p7	3:47468285	TTCTAGATCCTTGAG[C/G]AATCGCCACACTGTC	22937
rs541557184	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime, downstream-variant-500B	PTPN23, SCAP	GRCh38.p7	3:47413697	AGCTCCCAAAGTGCC[C/T]GACAGATGATGATAT	22937
rs541563249	in-del	-/T	0.00279162	0.0372561	intron-variant	SCAP	GRCh38.p7	3:47436721	TAGAAATAACTTCTA[-/T]TATAGTACAATGCAC	22937
rs541665315	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47451941	TGCCAACCTCATTCC[C/T]ATCTCAGGGGCCTGG	22937
rs541741545	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47443587	TCACTCGTGAAGAAG[A/G]TCTAGCGAGGTCAGC	22937
rs541759813	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47421123	AGCCACCTCATAACC[A/G]GCAGGGCAGCAGCAG	22937
rs541764046	snp	C/T			upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47476810	ACTAGAGACGCTGCC[C/T]GGACCACTCTGGGGG	22937
rs541794260	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47477657	ACTCCTTTACCCAGG[C/T]TGGAGTGCAGTGGTG	22937
rs541800890	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47428354	GCCACCGTAGACCCA[C/T]AAGGATGCTGAGAAA	22937
rs541829747	in-del	-/AGAA	0.00119737	0.0244387	intron-variant	SCAP	GRCh38.p7	3:47421442	GATTCAGGGGCTCTC[-/AGAA]AGGTTCCCAGCCAGC	22937
rs541831663	snp	A/T			intron-variant	SCAP	GRCh38.p7	3:47456180	AGTCAAGGCAGACAG[A/T]TCACTTGAACCCAGG	22937
rs541842677	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47469140	ATCACTTGAGGTCAG[A/G]AGTTCAAGACCAGCC	22937
rs541888643	snp	C/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47436562	TAACCCTGGGAGGTA[C/G]AGGCTGCAGTGAGCT	22937
rs541888984	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47427782	ATTTGCTCTCTGGTA[C/T]CGCCAAAGAGCCTGA	22937
rs541903369	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47467344	GTGGGGTGGCTCATG[C/T]CTGTAATCCCACCAC	22937
rs541905963	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47420175	CCAGCCCGGCTGGTG[A/G]ATGATTTTGCCCAGC	22937
rs541953386	snp	C/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47461081	AGCCTCCCCTCTGTA[C/G]CCCCTCCATGCCCAC	22937
rs541964374	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47443196	GGAATGGTTTCAGAA[C/T]GCCTATATGCAAGGT	22937
rs541968536	in-del	-/C	0.00199481	0.0315187	intron-variant	SCAP	GRCh38.p7	3:47473365	CACCCAGAATTATTA[-/C]CTCTGAGTGGCAAAA	22937
rs542024204	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47444450	AGCAGAAGCGTTAAG[C/T]GCACATGCAAGTTTC	22937
rs542031291	snp	A/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47472138	TCAAAAAAATAATAA[A/T]AATAATTAAATGGGG	22937
rs542061341	snp	C/T	0.00159617	0.0282053	intron-variant	SCAP	GRCh38.p7	3:47453438	CCCCTTGCACAAAAG[C/T]TCTGAATGGCTCTCC	22937
rs542136072	snp	A/C	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47455649	CTGAAACTCCGAAAG[A/C]CAGAAAAGATGACTT	22937
rs542181904	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47442024	TTCATCTTTCTTACT[A/G]ATAATCAGGGAAGAG	22937
rs542293768	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47442609	TATTTCAGTGTCTTA[A/G]AAGTATCTAAACATT	22937
rs542302046	snp	G/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47452717	AATTTGAGAAACACT[G/T]CCCTACCAAACCTGG	22937
rs542397949	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47443396	CTCATGTGTGGCACA[C/G]GAAACCATGCCTGTG	22937
rs542414666	snp	A/G	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47443765	TACCCGTCCCCTTCC[A/G]TAAGTTAACAGCAGC	22937
rs542455001	snp	C/G	0.0023933	0.0345097	intron-variant	SCAP	GRCh38.p7	3:47433953	GAGCCAATGGCCAAC[C/G]TGGGACATAAAGCCA	22937
rs542473537	snp	A/G	0.00119737	0.0244387	intron-variant	SCAP	GRCh38.p7	3:47468532	TTTTGAGAAGTGTCT[A/G]TTCATATGCTTCACC	22937
rs542613649	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47450433	AATAAAAATTATATA[C/T]AAAAAGTGCACAAAA	22937
rs542628262	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47424104	TCCCAACAGACTGGG[A/G]CCCTCAGGAAGGCTG	22937
rs542695592	snp	A/G			downstream-variant-500B	PTPN23, SCAP	GRCh38.p7	3:47413578	GGGCCCTGCAGTTCT[A/G]GCTTGCTCATCCTCC	22937
rs542816229	snp	C/T	0.000264317	0.011493	intron-variant	SCAP	GRCh38.p7	3:47418627	CTCCCCGCACTCTTT[C/T]CCACCCCACCCCACC	22937
rs542922334	snp	C/T	0.000477171	0.0154388	synonymous-codon	SCAP	GRCh38.p7	3:47419624	CAATGGGCTCTGTTC[C/T]GTCACCTGGGCAGCG	22937
rs542980106	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47458933	GCCTCAGCCTCGCAA[A/G]TAGCTGGGATTACAG	22937
rs542985550	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47429399	GGTCTTGCTCTATTG[C/T]CCAATCATGGCTCAC	22937
rs543013256	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47432074	AATCCCAGCACTTTG[A/G]GAGGCCGAGGCGGAT	22937
rs543021034	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47471515	AGGTATACTACAGGC[A/G]CATGCCACCACACCT	22937
rs543052062	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47431356	AGAAGGACATTTCAT[C/T]TCTGTAGTCCTCCTT	22937
rs543093229	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47426342	GCACTGGGAAAATCA[C/T]AAAGGGGACAAAGTT	22937
rs543103159	snp	A/C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	SCAP, LOC105377073	GRCh38.p7	3:47475167	CGACTCACTGCCCCC[A/C/G]CCTCCGCATTCCCAT	22937
rs543183620	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47467988	GGTTTTCTGTCCTTG[C/T]GATAGTTTGCTCAGA	22937
rs543263237	snp	C/T	0.00122449	0.0247133	utr-variant-5-prime, intron-variant, upstream-variant-2KB	SCAP, LOC105377073	GRCh38.p7	3:47475823	CAGCACCTCCCAAGC[C/T]GCGGCGGCGGCGGCG	22937
rs543264932	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47461127	TTTCATCCTGCTCAC[C/T]GCTGGCCCTAAGACT	22937
rs543299514	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47459740	GAACTACTGATAAGG[A/G]TCTATGTTCAGCTGT	22937
rs543331808	snp	A/G	9.90311e-05	0.00703603	missense	SCAP	GRCh38.p7	3:47420939	CTCCTACCTCCATCC[A/G]GCGAATGTCAATGGA	22937
rs543366249	snp	A/G	0.00557542	0.0525036	intron-variant	SCAP	GRCh38.p7	3:47415384	TCAGTTTCTTCATCC[A/G]TAAAATGGGGATAAG	22937
rs543369876	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47434015	GCCAGCATCAGACCA[C/T]GCATCCTTTGACCTT	22937
rs543382417	in-del	-/AGGAAGGGGCTGAAAGT	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47425795	TAGGAACCCTAACCC[-/AGGAAGGGGCTGAAAGT]AGGAAGGGGCTGAAA	22937
rs543620967	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47477040	GCAAGGCAGAAATTA[C/G]AGGTGGCCCTTCTGA	22937
rs543622809	snp	A/G	8.30337e-05	0.00644282	intron-variant	SCAP	GRCh38.p7	3:47414657	AGACGGAACACCTGG[A/G]ACAGGGATGGGCCTC	22937
rs543715859	snp	C/G	1.69648e-05	0.00291241	intron-variant	SCAP	GRCh38.p7	3:47414401	TCTGGGGAAACAGGC[C/G]AGGGGAGTGGGGTCA	22937
rs543779273	snp	G/T	0.00199481	0.0315187	upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47477569	GAGCGAGACTCCGTC[G/T]CAAAAAAAAAAAGAA	22937
rs543794993	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47425292	CACTATAGCTAGATA[C/T]GCTATATACAAACAC	22937
rs543837785	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47447601	GCGGAGACAGGAGAA[C/T]TGCTTAAACCCGGGA	22937
rs543860798	snp	A/G	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47467598	GAGCAAGAAGACCCC[A/G]TCTCAAGAAAAAGAA	22937
rs543875621	snp	C/T	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47432950	AGGTAACCCTATTCA[C/T]AGCCAACTGGGCTCC	22937
rs543881566	snp	C/T	0.00159617	0.0282053	intron-variant	SCAP	GRCh38.p7	3:47424720	TTTAACAGTGTCAAG[C/T]TCAGGAAAGGGAGCA	22937
rs543894943	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47470077	ACTACTTTTAAGTGT[A/G]TATACAGATGGCTCT	22937
rs543934912	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime, intron-variant, upstream-variant-2KB	SCAP, LOC105377073	GRCh38.p7	3:47475837	CTGCGGCGGCGGCGG[C/T]GGCGGCGACGGGGGC	22937
rs544006040	in-del	-/A	0.0146672	0.084371	intron-variant	SCAP	GRCh38.p7	3:47455595	GCAAGACTCCACCTC[-/A]AAAAAAAAAAAAAAA	22937
rs544077345	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47440007	ATTCCCAAGCTGTCA[C/T]TGATCACCATCCCCC	22937
rs544280912	snp	A/G	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47429335	GTGTAGGCAAACGAT[A/G]GCCTGTAGGCCAAAT	22937
rs544281576	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47446362	ATTTTTAGTAGAGAC[A/G]AAGTTTCACTATGTT	22937
rs544350224	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47423150	GATGAATGGACGGCT[A/G]CCTACAGCCCCATTC	22937
rs544358058	snp	G/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47440879	GAAGAAAAAAAAGAA[G/T]GGGATAATACAGAAG	22937
rs544446908	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47430258	GTGTAAGGACTCAAA[C/T]CAAGGTCTCCTCACT	22937
rs544458255	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47452136	AGTGCATTTAAAACT[C/T]TGTAATTGTACAAAT	22937
rs544493530	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47432210	TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG	22937
rs544518274	snp	A/G	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47423860	GTTTGCTCACAGAGC[A/G]TTAACAGCAAGAGGA	22937
rs544562221	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47447116	TTGTCAAAAAGCAGT[C/T]GTCTGGACCAGGCAC	22937
rs544672892	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47438596	AGGTGGGTGGGTCAC[A/G]TGAGGTCAGGAGTTC	22937
rs544702477	snp	A/G	0.00199481	0.0315187	intron-variant	SCAP	GRCh38.p7	3:47441027	CTGCCTCAGCCTCCC[A/G]AGTGGCGGGGACTAC	22937
rs544816671	snp	A/G	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47441852	AGCACCCAGCAAGAA[A/G]CTCTCAGTGATGTTC	22937
rs544857087	snp	C/G	0.00517822	0.0506191	upstream-variant-2KB, utr-variant-5-prime, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47476102	CGGGCCGGGCCGGGC[C/G]GGGCGGAGCGTGAAG	22937
rs544872037	snp	C/T	0.000798403	0.0199641	utr-variant-5-prime, intron-variant, upstream-variant-2KB	SCAP, LOC105377073	GRCh38.p7	3:47475852	CGGCGGCGACGGGGG[C/T]GGCAGCAGGGGCGGA	22937
rs544876912	snp	G/T			intron-variant	SCAP	GRCh38.p7	3:47443890	TGGGCCTCTCTCCCT[G/T]GACTTTGACTTCTAA	22937
rs544887580	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47432392	ACTGACCACTGGGGA[A/G]CTCTTTCGATTGCCC	22937
rs545011894	snp	C/T	0.00159617	0.0282053	intron-variant	SCAP	GRCh38.p7	3:47458874	GCAACGGCGTGATCT[C/T]GGCTCACTGCAACCT	22937
rs545016152	in-del	-/TATATATATA			intron-variant	SCAP	GRCh38.p7	3:47455086	ATATATATATATATA[-/TATATATATA]ATCAACTGAAAACCT	22937
rs545082587	snp	C/T	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47423239	GGCTCTCCCTTTTCT[C/T]ATTTTCCCTAGAACC	22937
rs545156613	snp	C/T	0.000476531	0.0154285	missense	SCAP	GRCh38.p7	3:47417492	GGGCTGGTGTGCAGA[C/T]GGCCGCCAGCCCCTC	22937
rs545311680	snp	G/T	0.00135695	0.0260122	intron-variant	SCAP	GRCh38.p7	3:47418099	GGTGAGGGGGGTTGT[G/T]GGGGCACAAAGGAGG	22937
rs545336198	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47457933	ATAAAAAGAAAATTG[C/T]TTCTCTAAGCTTCAA	22937
rs545359214	snp	C/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47439488	GAGCAGCAGCTTGTT[C/G]AATCAAATGTCTCAA	22937
rs545367189	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47463476	GGAGGCAGAGGCAGG[C/T]GGATCACTTGAGGTC	22937
rs545418339	snp	C/T	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47465500	GGCCAGGCACGGTGG[C/T]CCATGCCTGTAAACC	22937
rs545532825	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47463691	AGCCTAAGTGACAAA[A/G]TGAGACTGTCCCTAA	22937
rs545577065	in-del	-/AA			intron-variant	SCAP	GRCh38.p7	3:47448032	AAAAAAAAAAAAAAA[-/AA]CTTGATAGAATTTTG	22937
rs545597221	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47474189	AGAATCGCTTGAACC[C/T]GGCAGGCGGAGGGTG	22937
rs545620627	snp	A/C	0.00279162	0.0372561	intron-variant	SCAP	GRCh38.p7	3:47472268	GAAACCCCGTCTCTA[A/C]TAAAAATACAAAAAA	22937
rs545650847	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47423508	AAGCAATCCTCCCAC[A/C]TCAGCCTCTTGAGTA	22937
rs545754806	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	SCAP, LOC105377073	GRCh38.p7	3:47475116	GAGCAGTGAGTGACC[C/G]GAACCAGGGGCTGAC	22937
rs545761227	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47471481	GAGGAAAACATCAAC[A/G]TAGTTCTAGTATACT	22937
rs545770810	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47416043	CAGAACCTGTGGTGA[C/T]AGGAATGACGGCAGC	22937
rs545824412	snp	C/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47429262	TTCTAGCACATTGGG[C/G]AGCGAGCCTCTTTTG	22937
rs545843185	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47416600	CCCTATTCCAAGCAC[A/G]TCACACCCCTAACGC	22937
rs545856204	snp	A/G	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47421908	TCACAGCCCACAGCT[A/G]AGTGAGGGCACTTTG	22937
rs545874639	in-del	-/G	0.00318978	0.0398085	intron-variant	SCAP	GRCh38.p7	3:47422746	GCTGCTACGGGGAAC[-/G]GGTGTTCACAGCCTG	22937
rs545891614	snp	C/T	0.0023933	0.0345097	intron-variant	SCAP	GRCh38.p7	3:47444627	TACAGGTGTGCACCA[C/T]CATGCCCTGCTAATT	22937
rs545891715	snp	C/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47454361	CGAAAGAGTGAGACT[C/G]CGTCACAAAAAAAAA	22937
rs545930094	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47416515	TTCATTGAGAAGGGC[A/G]AGAAAGGATAGGAGT	22937
rs545930434	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47453524	ATATACTGAAACCTC[C/T]TTCCAGCTTTATTCT	22937
rs546044257	snp	A/C	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47455731	GTAACCAAAGTGTCA[A/C]TCTTCCTACATTCAT	22937
rs546045738	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47436904	CTGTTAGAATCTCTA[C/T]CACCATAAATTAGTT	22937
rs546051717	snp	G/T	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47478672	AGTAGAGACAGAGTT[G/T]CGCCATGTTGGCCAG	22937
rs546070199	snp	G/T			intron-variant	SCAP	GRCh38.p7	3:47440680	TTGAGACCAGCCTGG[G/T]CAACATGGCGAAACC	22937
rs546153753	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47446464	GCGTGAGCCACCGTG[C/T]CTGGCCCCCCTCAAT	22937
rs546155653	snp	A/G	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47456958	TTGGGAGGCTGAGGC[A/G]GGTGGATCACCTGAG	22937
rs546261314	in-del	-/C	0.00119737	0.0244387	intron-variant	SCAP	GRCh38.p7	3:47428340	CCAAGCGGAATGCAG[-/C]CACCGTAGACCCACA	22937
rs546297077	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47455173	TATCAATGCCTTCAC[A/G]TACATCAACAACAAG	22937
rs546422290	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47457543	AACTAGTCCACTGGT[A/G]CAAACAATTCATCCC	22937
rs546444354	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47429506	TGTGTGCACCACCAC[C/T]ACGCCTAATTTTCAA	22937
rs546556790	snp	C/G	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47422679	ACCAAAGCACCCCAA[C/G]CCTCAGGGTCCTGCT	22937
rs546609012	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47444771	CGAACCACCACACCC[A/G]GCCAGTACTTCATTA	22937
rs546610906	snp	A/G	4.95487e-05	0.00497714	intron-variant, utr-variant-5-prime	SCAP	GRCh38.p7	3:47434969	GCCAGTCTCCACCCA[A/G]CGCTCTGTGCTGGCC	22937
rs546667899	snp	A/G	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47446583	CTTAGGAGTGGAATT[A/G]CTTGGTCATAAGGTA	22937
rs546686472	snp	A/G			intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47426789	TCAGAAGCACCTCGA[A/G]TGCCCTTGCCAATTG	22937
rs546704697	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47455947	CAGATTAATGTAACA[A/G]AACAGAATGTCCAGG	22937
rs546709611	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47437307	AGCCGGGCGTGGTGG[C/T]GTATGCCTGTAATCC	22937
rs546721601	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47435990	AGAGGTAGAGGCTGC[A/G]GTGAGCCATGATTAT	22937
rs546784103	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47434243	TCTGTTCGCTGAGCT[C/T]TGGTTTTCCTCAACA	22937
rs546821551	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47437924	GAGCTTAGTAGATGA[C/T]ACCAAACAGTTTTCC	22937
rs546824897	snp	G/T	0.00358779	0.0422022	intron-variant	SCAP	GRCh38.p7	3:47454663	GAACGCAGGAGAATC[G/T]CTTGAACCCAGGAGG	22937
rs546889844	snp	C/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47421236	CAGAAGAAACCCTCA[C/G]ACTTTCTTCAGAAAG	22937
rs546890813	snp	A/C	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47472846	AGCACTTTGGGAGGC[A/C]GAGGCGGGCGGATCA	22937
rs546895213	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47430577	GATAACAGAAATTAC[A/G]AGGAAGATGACAAGC	22937
rs546935552	snp	C/T	0.00119737	0.0244387	intron-variant	SCAP	GRCh38.p7	3:47471590	TGGTCAGGCTGGTCT[C/T]GAACTCCTGACCTCA	22937
rs546964056	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47419835	ACACAGGCCCCACTG[C/T]GTCCTTTTCTCCTGC	22937
rs547001053	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47419263	TGTGGGCCTCCTGCA[C/T]TGGGGAAAGGGGATG	22937
rs547074775	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47430291	ATATCACATACTTTT[C/G]TCACTAGAATCTGCC	22937
rs547075542	snp	A/G	0.0007024	0.0187272	intron-variant, utr-variant-3-prime, downstream-variant-500B	PTPN23, SCAP	GRCh38.p7	3:47413852	GCAAGGAGGCCCTGC[A/G]CTCAGTCCAGCTTCT	22937
rs547088506	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47426465	ATTTTTTGAGACAAG[A/G]GTCTCGCTGTCGCCC	22937
rs547144110	snp	C/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47421928	AGGGCACTTTGCCAA[C/G]AGCAGGGTCACTCTG	22937
rs547189252	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47415338	GATGCTGGAGCCAGA[A/G]GGCAACTCCAAATAT	22937
rs547237166	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47414499	CTGGAAGGCCCCTGG[A/G]GACCAGCTCCCAGGA	22937
rs547247172	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47443972	GGTTCCTGCTCCCAA[A/G]ATCCCCAGGCTGTTC	22937
rs547405808	snp	C/G/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47457689	GAGGTGGGTGGGTCA[C/G/T]GAGGTCAGGAGATCG	22937
rs547424681	snp	C/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47460665	CAGGTTCAAGCGATT[C/G]TCCTGCCTCAGCCTC	22937
rs547561256	snp	C/T	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47468774	ATTGCTTTTGGTGTT[C/T]TAGTCATGAAGTCCT	22937
rs547586601	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47452376	AAACAAACCACTTGT[C/T]GAATAAGTGATGAAC	22937
rs547641461	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47415235	AGCCCCAGCCCTGGG[A/G]CTGAGCATGTGGACA	22937
rs547663289	in-del	-/AA			intron-variant	SCAP	GRCh38.p7	3:47455701	ACATTCTTAATGAGG[-/AA]AAGTCAATATAACGT	22937
rs547709418	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47461833	CAGGTCAGGAGTTTG[A/G]GACCAGCGTGAGCAA	22937
rs547767949	snp	A/C	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47434072	GTGGTGCACTCCCCA[A/C]TGACACCATGTATAG	22937
rs547827352	snp	C/T	6.63592e-05	0.00575979	synonymous-codon	SCAP	GRCh38.p7	3:47414590	GTCAATGTACACGGT[C/T]GTGATGGCCCCTGAG	22937
rs547870603	snp	C/T	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47441195	GTGAGCCACCACGCC[C/T]GGCCAGGTCTTTCCT	22937
rs547914609	snp	A/C	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47420469	GGAATACCCTTTGCC[A/C]CTCTAAGGCCAAGTG	22937
rs547928921	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47427685	GCACAGGAGACAGGA[A/C]AAGGCACCTGCTGTG	22937
rs547939718	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47451875	CCGGTCCTCTGCAAC[C/T]TCACTTCGTGTCACC	22937
rs547955801	snp	C/T	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47449493	TCCTCTCCTATCCAT[C/T]TGCCAATGTCACTGC	22937
rs548032552	snp	C/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47442365	CCTTGGCAAGTGCAG[C/G]TGGCCACAAGAATCA	22937
rs548067579	snp	C/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47425769	CCAGTGTCATGGACA[C/G]AGTACACCTTTTAGG	22937
rs548098385	snp	C/T	0.00119737	0.0244387	intron-variant	SCAP	GRCh38.p7	3:47454105	GGGTGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC	22937
rs548195185	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47469340	TGACAAGGAGACTCC[A/G]TCTCAAAAAAAAAAT	22937
rs548215967	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47444931	TGCCCGCCACCACAC[C/T]TGGCTAATTTTTGTA	22937
rs548220433	snp	C/G	0.00159617	0.0282053	intron-variant	SCAP	GRCh38.p7	3:47453112	AAAATAAAAAATGAA[C/G]TGGACTAGTGATAGA	22937
rs548237567	snp	G/T			synonymous-codon	SCAP	GRCh38.p7	3:47419435	GGTTACCTCTGGGAC[G/T]GGGCTGTCATGGACA	22937
rs548270125	snp	C/G/T			intron-variant	SCAP	GRCh38.p7	3:47447961	AGTAAGCTGAGATAG[C/G/T]GCCACTGCACTCCAG	22937
rs548288835	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47433349	CCTGCAGGGGATGAG[C/T]GCTCCAATCAGAGAG	22937
rs548354372	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47461387	GGTACTAAGTAAAAC[C/T]TTCCAGCTAACAGGA	22937
rs548455124	snp	C/T	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47445610	GGAATCTTGCTTTGT[C/T]GCCCAGGCTGGAGTG	22937
rs548478732	in-del	-/A	0.00119737	0.0244387	intron-variant	SCAP	GRCh38.p7	3:47445146	CATTCATCAGTTGAT[-/A]AAACATTTGGGCAGT	22937
rs548540532	in-del	-/AAAAA	0.00279162	0.0372561	intron-variant	SCAP	GRCh38.p7	3:47452926	AGATCCTGTCTCTAC[-/AAAAA]AAAAAAAAAAAAAAT	22937
rs548571858	snp	A/C/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47441091	ATTTTTAGTAGAGAC[A/C/G]AGGTTTCACCATGTT	22937
rs548573281	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47477332	GGGAGGCCAACACGG[A/G]CAGATCATGAGGTCA	22937
rs548573757	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47431693	CGGTAAAATGTCCTC[C/T]TCCTCCTCACATATC	22937
rs548578432	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47451141	TACAGACATGAGCCA[C/T]CGTGCAAGACTATTT	22937
rs548592415	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47473889	TGACTGAGGGAACGG[A/G]GGAAGGGCCCCAAAC	22937
rs548763684	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47426528	CTGCAAGCTCCGCCT[C/G]CTGGGTTCACACCAT	22937
rs548767810	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47434730	CAGTCCCAGCTAATC[A/G]GGAGGCTGAGGCAGG	22937
rs548815915	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47450021	TTCTTTTTTTGAGAT[A/G]GAGTCTTGCTCTGTC	22937
rs548817178	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47459817	CAAGAGCAGAGAACC[A/G]GTCTGACCTCAAATT	22937
rs548819620	snp	A/T			intron-variant	SCAP	GRCh38.p7	3:47445806	AGAACTCCTGACCTT[A/T]GATGATTTGCCAGCC	22937
rs548827020	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47435439	TTAGTTATAACATTA[C/T]ATATAACATTAACAT	22937
rs548840428	snp	C/T	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47419886	ACACCTGCCAACACT[C/T]GCTGCTGGAGGGGCC	22937
rs548875099	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47476563	ATAGACATTTAAAAG[C/T]ATAAGTTGACATTTA	22937
rs548876617	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47426930	AGGACACTGAGACCG[C/T]CAGCCCTACCTTAGT	22937
rs549005628	snp	G/T	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47416831	CGGGGTTTCACCGTT[G/T]TAGCCGGGATGGTCT	22937
rs549039010	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47424844	CATAATCCATTAATA[A/G]CCATTAATAGACAGG	22937
rs549056706	snp	C/G			intron-variant, upstream-variant-2KB	SCAP, LOC105377073	GRCh38.p7	3:47475789	GCCCTGAGCACCCGC[C/G]TGACGGTACCTGTGG	22937
rs549070843	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47458204	TTGGGAGGCCAAGGC[A/G]GGTGGATCACGAGGT	22937
rs549194330	snp	G/T	0.000399281	0.0141238	missense	SCAP	GRCh38.p7	3:47417538	CTGCACCAGGCAGCT[G/T]AAGTCATAGCCTGGG	22937
rs549259074	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47440230	TCTAGCAAAACTACT[A/G]GAAGCAGTCTATATC	22937
rs549311683	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	PTPN23, SCAP	GRCh38.p7	3:47413251	CACCTGCCCACACCC[A/C]GCAGAGCTTCTCAGT	22937
rs549375075	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47424975	ATCAGTGAAAAAGGC[A/G]ACAAATTACAGTGTG	22937
rs549381687	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47473690	CACATTCACATGCAT[A/G]GCTAGATTCTGAGAG	22937
rs549402764	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47449121	CGTCCAGGGGCCAGT[A/G]CAGAACTACTTGAGC	22937
rs549444681	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47419177	TCCTCTCTTGGGTTA[C/T]AGCTGCCTAAACCAC	22937
rs549514347	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47433263	ATCAAGGACAGCCAA[C/T]GGAGGTGAGATAACT	22937
rs549545504	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	SCAP, LOC105377073	GRCh38.p7	3:47474405	ATACAGTGTTAAATA[C/T]ATTTATATAGTGTTT	22937
rs549545608	snp	C/T	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47464909	AGCTAATAAATGAAT[C/T]CAACAAAGTTGTAGG	22937
rs549576043	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant, nc-transcript-variant	SCAP, LOC105377073	GRCh38.p7	3:47476323	TTAATTAGCCGGCTG[A/T]GGTGGCGCGCACCTG	22937
rs549624505	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47452177	CTGGTTTACTATCTG[C/T]CCTCTGTCAAGACTA	22937
rs549679099	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47448295	ACATTGATTTTTTTA[C/T]GTTAATCTTTTATCC	22937
rs549688033	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47468572	ATAGGGTTGTTTGAT[C/T]TTTTTCTTGTAAATC	22937
rs549974406	in-del	-/ACTTGCTTTC	0.0146672	0.084371	intron-variant	SCAP	GRCh38.p7	3:47438501	TTACTTTTCTAATAA[-/ACTTGCTTTC]ACTTAAAAAAAAGTT	22937
rs549992169	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime, downstream-variant-500B	PTPN23, SCAP	GRCh38.p7	3:47413350	GTGGAAATGTACTGC[A/G]GGCTCTGGGTCAGGT	22937
rs550192974	snp	C/G	0.000399281	0.0141238	synonymous-codon	SCAP	GRCh38.p7	3:47417580	GCGGCCACAGACCGC[C/G]CGGTGCCGGGGCTCG	22937
rs550196329	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47442186	AAAGAATAAGATGGG[C/T]TCTTTTCACAGCTGT	22937
rs550357150	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47439930	TGTTTGGGGTGAGCC[C/T]GATGCATATACAGAT	22937
rs550447495	snp	A/T	0.00795532	0.062565	intron-variant	SCAP	GRCh38.p7	3:47432669	TATTTTCCCTTTTTT[A/T]AAATTTATTTATTTT	22937
rs550467989	in-del	-/CAG	0.00199481	0.0315187	upstream-variant-2KB, intron-variant, nc-transcript-variant	SCAP, LOC105377073	GRCh38.p7	3:47476344	GCGCACCTGTGGTCC[-/CAG]CAGCTACTCAGGAGG	22937
rs550524271	snp	A/G	0.00199481	0.0315187	intron-variant	SCAP	GRCh38.p7	3:47428728	AGGAAGAAGAAAGAC[A/G]GTCCAATTCAAGGGA	22937
rs550563042	snp	G/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47437157	ATTAAGAATAAAGTT[G/T]GGCCAGGCACAGTGG	22937
rs550563257	in-del	-/TTTG	0.00398564	0.0444627	intron-variant	SCAP	GRCh38.p7	3:47469368	AATCACCAAATAATT[-/TTTG]TTTGTTTGTTTTGAG	22937
rs550579891	snp	A/C	1.79406e-05	0.00299499	intron-variant	SCAP	GRCh38.p7	3:47417280	CGGACAGCCGCTCTG[A/C]CCACCTTTAGCCCCT	22937
rs550604363	snp	A/T	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47473870	TTTACCCACCTAATG[A/T]CAGTGACTGAGGGAA	22937
rs550676601	snp	A/C	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47447533	TCTCTACTAAAAATA[A/C]CAAAATTGGCTGGGT	22937
rs550688525	in-del	-/T			intron-variant	SCAP	GRCh38.p7	3:47444023	GACTGGCTCATCAAC[-/T]TTTTTTTCCGTTTTG	22937
rs550762272	snp	A/C	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47423603	TTCACCATGTTGCCC[A/C]GGCTGGTCTTGAACT	22937
rs550777450	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47421991	CCAGGCAAGGCCATG[C/T]GTCTGGCGACTGCGG	22937
rs550797885	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47478898	GTGCCTCAACCTCTT[A/G]AGTAGCTGGGACTAC	22937
rs550800214	snp	C/T	6.88362e-05	0.00586629	intron-variant	SCAP	GRCh38.p7	3:47422583	CACATGGCCACTCTG[C/T]GACATGACTCACACA	22937
rs550814837	snp	A/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	SCAP, LOC105377073	GRCh38.p7	3:47474540	TGGTTCACGCCTGTA[A/T]TACCAACACTTTGGG	22937
rs550874334	snp	G/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47424311	AGGAGGGCTGGAAGA[G/T]GCCCCTCAGGGAGAG	22937
rs550936480	snp	C/T	0.00159617	0.0282053	intron-variant	SCAP	GRCh38.p7	3:47416204	ACAGGCAGGCAAAGG[C/T]GTCCGGCAGAAGGCA	22937
rs550992058	snp	C/T	0.000759138	0.0194677	synonymous-codon, intron-variant	SCAP	GRCh38.p7	3:47423979	TACCGGGGTTGAGAC[C/T]ACAGACTTGGTGAGC	22937
rs551105644	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47416712	GCTCACTGCAAGCTC[C/T]GCCTCCCGGGTTCAC	22937
rs551218887	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47430800	GGCAGGGCCCAGCCC[A/G]GCTGAGGGATGAGGG	22937
rs551219913	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47471358	TAAAACCTGAGACAA[A/G]GAGCAGAAACCATTA	22937
rs551257342	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47424773	ACCAGAAACAAAATA[C/T]GACGTCGCTTTTCAT	22937
rs551268597	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	SCAP, LOC105377073	GRCh38.p7	3:47475338	GAGGTTTAAGCAATA[C/T]GGAAAACTAGAAACC	22937
rs551327629	in-del	-/AGCTA			intron-variant	SCAP	GRCh38.p7	3:47466667	AAATGAAAAAAGAAG[-/AGCTA]AAACTGTAAAGCCCT	22937
rs551337421	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47468937	TCAGCTTTCTACATA[C/T]GGCTCCTGGATCGAT	22937
rs551367097	snp	C/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47422007	GTCTGGCGACTGCGG[C/G]ACAGGCCAGGGCCAA	22937
rs551425070	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47430715	AAAGACTCCCCGGGA[C/G]TTGGTGACAACTGGA	22937
rs551442662	snp	C/T	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47416787	GCCCGCCACTACGCC[C/T]GGCTAATTTTTTGTA	22937
rs551450328	snp	C/T	0	0	intron-variant	SCAP	GRCh38.p7	3:47431503	TACGTTTAGCTGTAG[C/T]GTCTGAGGCTTCTTG	22937
rs551465247	snp	A/C			missense	SCAP	GRCh38.p7	3:47418808	CTCGGGTTCAGGCGG[A/C]GCGTGACTGGGATGA	22937
rs551504148	snp	G/T			intron-variant	SCAP	GRCh38.p7	3:47415625	CAACCCAAGCACAGC[G/T]CACATCAATTCCTTT	22937
rs551541348	snp	C/T	0.00119737	0.0244387	intron-variant	SCAP	GRCh38.p7	3:47456729	GAGATCATCCGAGAT[C/T]GTGTGAGATCGTGCC	22937
rs551551586	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47464071	CCCAGGCTGGAGTAC[A/G]GTGGCATGATCTCAG	22937
rs551565958	snp	C/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47424403	TAAAGACAATGACTG[C/G]TGCCAAGACCCACAC	22937
rs551616921	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47447603	GGAGACAGGAGAATT[A/G]CTTAAACCCGGGAGG	22937
rs551621824	snp	A/G	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47466859	GAAGCCAAGGCAAGC[A/G]GACTGCTTGAGCTCA	22937
rs551627356	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47460880	AATATAAACGTTGCA[C/T]GGAAGAGGGTTCCAA	22937
rs551762602	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47429383	TTTCTTTTTGAGACA[A/G]GGTCTTGCTCTATTG	22937
rs551828782	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47479060	TGACCCACCATGCCC[A/G]GCCTCCTACAACATT	22937
rs551865657	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47473557	TCTCATCTGTTCAAC[A/G]GGGGTGATGACACAA	22937
rs551911043	snp	C/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47472715	CATCCCCACACTAGA[C/G]TCAGTGACGCTGGCT	22937
rs551930511	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47464837	TAGTAAAATTATTTC[C/T]GTTCCTAGATGACAT	22937
rs552186887	snp	C/T			intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47426711	CAAAGTCTGGGATTA[C/T]AGGCGTGAGCCACCG	22937
rs552262502	snp	A/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47454880	GTGTTCTCACTAACG[A/T]CAGGGGCCATACAGG	22937
rs552289452	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47462748	ATAAGAGCGAAACTC[C/T]GTCTCAAAAAAAAAA	22937
rs552319605	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47415821	ATGAATTTGAAGGGC[C/T]TGCACCAGAGCTGGG	22937
rs552388065	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47434768	CTTGAACCCGGGAGG[C/T]GGAGGTTGCAGTGAG	22937
rs552414049	in-del	-/A	0.00119737	0.0244387	intron-variant	SCAP	GRCh38.p7	3:47459420	TACTACTTCAATATT[-/A]GGGGAACCCACCCCC	22937
rs552424222	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47445732	GCACACCACCACACT[C/T]GGCTAATTTTTGTAT	22937
rs552445225	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47437822	AAACTATTATCCTTT[A/G]TTGGTTTTTGGTGGC	22937
rs552556049	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47436103	CTAAAAACAAACAAA[A/C]AAAAATCACCTTGCC	22937
rs552561974	snp	C/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47470504	AAGAAAGCCTGACAA[C/G]TAGGCATCAGCTCCT	22937
rs552565742	snp	A/C	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47443149	CTCTGCACACTAGGG[A/C]TGCTGGAGGGAGGCG	22937
rs552605844	snp	G/T			intron-variant	SCAP	GRCh38.p7	3:47432482	TCTTTCCAAACAGTA[G/T]AGGATCTCCTCAAGG	22937
rs552675313	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47434234	GAGGAGAGCTCTGTT[C/T]GCTGAGCTTTGGTTT	22937
rs552786215	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47428337	GGTCCAAGCGGAATG[C/T]AGCCACCGTAGACCC	22937
rs552826240	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47416382	GAGGCAGGGAGAGCA[A/G]AGAACAGCTGCCAGC	22937
rs552853627	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47440963	CTAGAGTGCAGTGGC[A/G]CGATCTCAGCTCACT	22937
rs552888969	snp	C/T	0.00119737	0.0244387	intron-variant	SCAP	GRCh38.p7	3:47421184	TTGGTCCTCAGCTCA[C/T]ATACCAGCAGCAGCT	22937
rs553021915	snp	C/G	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47435347	TCACATAAACCTTAC[C/G]AAGAAGCCCAACTGG	22937
rs553057906	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47477454	CAGGTGCCTGTAGTC[C/T]CAGCTACTCGGGAGG	22937
rs553085256	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47441369	GCTTCTTAGGAGGCT[A/G]AGATGGGAGGGTCGC	22937
rs553095152	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47426732	TGAGCCACCGCGCCC[A/G]GCCTCCAACACTCTT	22937
rs553096387	snp	A/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47422047	CCGGAGGAAGGGTCT[A/T]GGAACCCCACGGTGC	22937
rs553134524	snp	A/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47436410	AGGCCAAGCGGGCGG[A/T]TCATTTGAGCTCAGG	22937
rs553171240	snp	C/T	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47465725	AGTGAGCAGTGACTG[C/T]GCCAATGCATTCCAG	22937
rs553203866	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47471172	GAATTTATCCCCTTA[C/T]AAATTTTAGCAAAAA	22937
rs553275084	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47461545	TCAGAGCTAGGAGAG[A/G]TGGGATCCTCCAGCA	22937
rs553277374	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47463437	CGGGGTGCGGTGGCT[C/T]GTGCCTGTAATCCCA	22937
rs553314157	snp	G/T	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47472074	TGCAGTAAACCAAGA[G/T]AGCATCAATGCACTC	22937
rs553323670	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	PTPN23, SCAP	GRCh38.p7	3:47413456	TGTCTGAGTCTGCCC[A/G]TTGCTGCCTCAGCTC	22937
rs553396814	snp	A/C	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47460926	GAGGAGTTTGTGAGG[A/C]GAAATGTGGCAAAGA	22937
rs553430838	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47453353	TTCGAGACCAGTCTG[A/G]GCAACATAGTGAGAC	22937
rs553479595	snp	C/T	1.66012e-05	0.00288103	intron-variant	SCAP	GRCh38.p7	3:47414173	CTATGATCCCCATCC[C/T]CTCTACCTGCTGAAT	22937
rs553492982	snp	C/G	0.00119737	0.0244387	intron-variant	SCAP	GRCh38.p7	3:47450314	TAAGGAAACTTTTCA[C/G]ACTACGCCTACTGGC	22937
rs553543256	snp	A/G	0.00119737	0.0244387	intron-variant	SCAP	GRCh38.p7	3:47451601	ATGGGGTTTTACCAT[A/G]TTGCCCAGGCTGGTC	22937
rs553584825	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47454260	TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG	22937
rs553628338	snp	A/C	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47460028	AGAATTTAGCGATAT[A/C]TTCCCTACTTGCATG	22937
rs553641059	snp	A/G	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47434462	TTCTCATTTATATCA[A/G]TGTTCGGCCCAGAGA	22937
rs553658008	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47444443	TTCCGAAAGCAGAAG[C/T]GTTAAGCGCACATGC	22937
rs553679652	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47443332	CCGCCCAACTCCCTC[C/T]CTCCTATATTAGGCA	22937
rs553938336	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47456190	GACAGATCACTTGAA[C/T]CCAGGAGTTCAAGAC	22937
rs554064062	snp	C/T	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47433784	GAGGCAGGAGAATCG[C/T]TTTCAACCCAGGAGA	22937
rs554079872	snp	A/G	0.000340271	0.0130392	missense	SCAP	GRCh38.p7	3:47418143	ACCTACCCTGGGCGC[A/G]GAATGCGCGTTAGGC	22937
rs554091792	snp	G/T	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47432810	AGTACTGGGATTACA[G/T]GTATGCACCACTGCA	22937
rs554191132	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47448497	CTTTTTGAGACTTCA[A/G]AAACATAAAAGATAA	22937
rs554196963	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47431891	CTTAGAATTTTTTTG[C/T]CCAGGAGATTTGTCT	22937
rs554203865	snp	C/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47425050	AGGCATTTAAATGTT[C/G]TAATCATGAAAAAAA	22937
rs554224132	snp	G/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47439517	AATGATTCACATCAC[G/T]CTCTGACCTGCACAT	22937
rs554351785	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47446876	TTGAGCCAAAGAGTT[C/T]GAGGCTGCAATGAGC	22937
rs554406361	snp	A/C	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47452418	CCCAACCAGGATCAG[A/C]TATTATTAGGACAGT	22937
rs554421168	snp	C/G			utr-variant-3-prime, downstream-variant-500B	PTPN23, SCAP	GRCh38.p7	3:47413274	TTCTCAGTGGGCACA[C/G]TCTCTTACTCCCATT	22937
rs554435479	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47427339	ACCCCTTTCTCACCC[C/T]CACCCTGGGAAACAA	22937
rs554472236	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47426772	AGGCCTAGGAGAGCC[A/G]ATCAGAAGCACCTCG	22937
rs554514184	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	SCAP, LOC105377073	GRCh38.p7	3:47475728	CCCCCATTCCGGAAC[C/T]CCCAGCTCCACGCGG	22937
rs554536201	snp	A/T	0.00119737	0.0244387	intron-variant	SCAP	GRCh38.p7	3:47451768	TCAGAGTGGACACAG[A/T]TTCTACTAATGCTGT	22937
rs554581393	snp	G/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47460786	TGGTCTTGAACTCCT[G/T]ACCTCGTGATCCACC	22937
rs554728984	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47430369	ACATATGCAACCCTC[A/G]GTAACAGGCATGTCG	22937
rs554750131	in-del	-/TT	0.00119737	0.0244387	intron-variant	SCAP	GRCh38.p7	3:47462108	TACTTCGTTTTGTGG[-/TT]TAAAAAAAAATTATT	22937
rs554832925	snp	C/T	1.65397e-05	0.00287569	synonymous-codon	SCAP	GRCh38.p7	3:47419387	GTGGCGGAAGGACAA[C/T]TTCCTCCAAAGTTCC	22937
rs554853436	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47476056	TCTCCCGTTCGCCCT[C/T]TGGTGGACACCGGAG	22937
rs554942306	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47474060	CATGAGGTCAGGAGA[C/T]AGAGACGATCCTGGC	22937
rs554974929	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47471558	TATTTATAGTGGAGA[C/T]GGGGTTTCACACATG	22937
rs555039524	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47425180	AAATCCGACTACACA[C/T]ATGCAATACATACTC	22937
rs555043927	snp	A/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47466320	GGTACTGGCATAAGG[A/T]CAGACATATAAAACA	22937
rs555055397	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47465257	TTCACTGCAATCTCC[A/G]CCTCCCAGGTTCAAG	22937
rs555070662	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47437755	CTCAAAAAAACAAAA[C/T]ATTTTGGGCTGGATA	22937
rs555074269	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47447054	CAATTGTTCCAGCAC[C/T]ATTTGGTGAAAAGAC	22937
rs555128135	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47432916	GCCTTTAGCCATAGG[A/G]CTTGGGAAGGGGACA	22937
rs555145704	snp	C/G/T	0.000112788	0.00750887	missense	SCAP	GRCh38.p7	3:47417815	CCCACGCCACTGTCC[C/G/T]GGCGCTGCCTGCTGG	22937
rs555150526	snp	C/T	2.27793e-05	0.00337478	synonymous-codon	SCAP	GRCh38.p7	3:47418663	GCCTTACTTGTACAG[C/T]GTGACGTCTCCATGG	22937
rs555170716	snp	C/T	0.000798403	0.0199641	utr-variant-5-prime, intron-variant, upstream-variant-2KB	SCAP, LOC105377073	GRCh38.p7	3:47475828	CCTCCCAAGCTGCGG[C/T]GGCGGCGGCGGCGGC	22937
rs555207887	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47425824	AAGTGGGAAGAGCCC[C/T]GGCCCCACCCAAGCT	22937
rs555209139	snp	C/G	0.00159617	0.0282053	intron-variant	SCAP	GRCh38.p7	3:47467508	TACTTGGAAGACTGA[C/G]GTGGGAGGATCACTT	22937
rs555296086	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47438173	GCAACTTTTGTGAAA[C/T]GCCTCTTCAAGTCTT	22937
rs555302221	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47468024	GGTTTCCAGCTTCAT[C/T]CATGTACCTATAAAG	22937
rs555306991	snp	C/G	0.00438332	0.0466095	intron-variant	SCAP	GRCh38.p7	3:47434740	TAATCGGGAGGCTGA[C/G]GCAGGAGAATCACTT	22937
rs555307517	snp	C/T	0.000798403	0.0199641	missense	SCAP	GRCh38.p7	3:47417429	CGGGGGAGCCACCCT[C/T]GTCCTCAGGGGCCTG	22937
rs555326910	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47449622	CCTGACCCATGAGGA[C/T]CCCCTTTCCTGCTCC	22937
rs555332953	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47441146	ACCTCGTGATCTGCC[C/T]GCCTCGGCCTCCCAA	22937
rs555342511	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47423812	ACTGCATATTATGCC[A/G]GAGGCAAGAGCAAGG	22937
rs555434558	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47422169	CTGAAAGGGAAGCAG[A/G]CAGGGAGGGGTAGGA	22937
rs555453643	snp	A/C	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47455591	CAGAGCAAGACTCCA[A/C]CTCAAAAAAAAAAAA	22937
rs555515491	snp	G/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47458412	CCAGCCTGGGCAACA[G/T]GGGCAAAACTCTGTC	22937
rs555549265	snp	C/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47462394	GTAAAGGCACACGCA[C/G]TGAAGCCTCCATTCT	22937
rs555553776	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47438579	AGCACTTTGGGAGGC[C/T]GAGGTGGGTGGGTCA	22937
rs555638682	in-del	-/GGCCG/GGCCGGGCCG	0.0209421	0.100162	upstream-variant-2KB, utr-variant-5-prime, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47476083	GAGGGAAGTATGGAC[-/GGCCG/GGCCGGGCCG]GGCCGGGCCGGGCCG	22937
rs555653226	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47440774	CTGAGGTAGGAGAAT[C/T]ACTTGAGCCCATGAA	22937
rs555665871	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47430165	TTCACTTCATCTGAC[C/T]CTCACAACAGCCTGA	22937
rs555670184	snp	A/C	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47439330	AAGAGAATCACTTGA[A/C]CCTGGGAGGCAGAGG	22937
rs555711337	snp	A/G/T	7.91962e-05	0.0062923	missense, synonymous-codon	SCAP	GRCh38.p7	3:47418482	GGCAGAGCAGCAGCA[A/G/T]CACCAAGACGATGCC	22937
rs555783498	snp	C/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47464134	AATTCTCCTGCCTTA[C/G]CCTCCTGAGTAGCTG	22937
rs555783793	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47447083	ACTATCCTTCCTCCA[C/T]TGAATTGCTTGGCAT	22937
rs555805729	in-del	-/ATTATAC	0.00517822	0.0506191	intron-variant	SCAP	GRCh38.p7	3:47436001	CTGCAGTGAGCCATG[-/ATTATAC]CACTGCACTCCAGCC	22937
rs555811825	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47459475	ATTTTCCGTAAGTGT[C/T]GGCCGGCTGAGAAAT	22937
rs555878108	snp	C/T	0.00199481	0.0315187	intron-variant, utr-variant-5-prime, upstream-variant-2KB	SCAP, LOC105377073	GRCh38.p7	3:47475589	AGGGGCCGGCCGGTG[C/T]AGGGACACGGCCGGG	22937
rs556086984	snp	A/C	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47451221	ATTATAAGCACACAG[A/C]TCCATGAATTACCAC	22937
rs556132448	snp	C/T	0.00438332	0.0466095	intron-variant	SCAP	GRCh38.p7	3:47418039	AGGGGTTGGGGGATA[C/T]CTCGGAGGAAGAAAG	22937
rs556145808	snp	A/G	0.00279162	0.0372561	intron-variant	SCAP	GRCh38.p7	3:47442516	CGCAACACACAAAAA[A/G]GGCTCTTGCACTTAA	22937
rs556434225	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47424602	AGAAAGTCTATGTGC[A/G]AGGAACGCCAGCCAA	22937
rs556495875	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47455702	CATTCTTAATGAGGA[A/G]AAGTCAATATAACGT	22937
rs556502508	snp	A/C	0.00358779	0.0422022	intron-variant	SCAP	GRCh38.p7	3:47440517	AAAATTAAAAAAAAA[A/C]CTTTAAGATCACATG	22937
rs556580658	snp	G/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47439404	ACAGAGTGAGACCCC[G/T]TCTCAAAATCAAAAA	22937
rs556664669	snp	A/C	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47447755	TTCATGCCTGTAATC[A/C]CAGCACTTTGGGAGG	22937
rs556747697	snp	C/T			upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47478724	CAGGTGGGATCCACC[C/T]GCCTCAGCCTCTCAA	22937
rs556786987	in-del	-/GAAAGG	0.00279162	0.0372561	intron-variant	SCAP	GRCh38.p7	3:47421255	TCTTCAGAAAGGGCT[-/GAAAGG]GAAAGGGAAGGGGAA	22937
rs556882126	snp	G/T	0.00199481	0.0315187	intron-variant	SCAP	GRCh38.p7	3:47416498	TAATCAGAGAAACTG[G/T]CTTCATTGAGAAGGG	22937
rs556984508	snp	C/T	0.00517822	0.0506191	intron-variant	SCAP	GRCh38.p7	3:47439621	TTCAGATTAACAGTA[C/T]CCTCTGTCTTGCTGG	22937
rs556999098	snp	C/T	0.00119737	0.0244387	intron-variant	SCAP	GRCh38.p7	3:47462316	GGTTTTTCTGTAAAA[C/T]AGTCATCTGACAGCC	22937
rs557036166	snp	A/G	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47461756	AGAGCAGTCTAGGCC[A/G]GGCACGGTGGCTCAC	22937
rs557067798	snp	A/G	0.0023933	0.0345097	intron-variant	SCAP	GRCh38.p7	3:47469948	GCTCTACTATTGTGA[A/G]GAGAGAAGCGGTTTT	22937
rs557083276	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47429608	CCCATTTTGGCCTCC[C/T]GAAGTGCCACACCTG	22937
rs557083597	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47422078	TTCTCCCTCAAAAAT[A/G]GGAAACAGGTGTGAC	22937
rs557084729	snp	A/G	0.0023933	0.0345097	intron-variant	SCAP	GRCh38.p7	3:47416869	CTGACCTCGTGATCC[A/G]CCCGCCTCGGCCTCC	22937
rs557108909	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47473034	GCAGTGAGCTGAGAT[C/T]ACGCCATTGCACTCC	22937
rs557119527	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47454333	AGATCACGCCACTGC[A/G]CTCCCATCTGGGCGA	22937
rs557219277	snp	A/G	0.00398564	0.0444627	intron-variant	SCAP	GRCh38.p7	3:47460836	GCTGGGATTACAGGC[A/G]TGAGCCACTGCGCCC	22937
rs557281096	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47455387	ATCACCTGAAGTCAG[A/G]AGTTAAAGACCAGCC	22937
rs557314737	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47478188	CTCACTCACCACCTC[C/T]TCCCACCCAACCACT	22937
rs557331886	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47436694	TTGTTTCAGATCTCA[C/T]TTTCTTAAAATTTAG	22937
rs557335416	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47467562	GTCAACTGTGATTGC[A/G]CCACTGCAGTCTGGG	22937
rs557400528	snp	C/T	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47473933	GTCCACGGAGATCTC[C/T]AGAGAGGGGGCGTTT	22937
rs557404653	in-del	-/C			intron-variant	SCAP	GRCh38.p7	3:47433236	CTTCAGTATCGCTGG[-/C]CCTGTATCTTTATCA	22937
rs557405316	in-del	-/AT	0.00199481	0.0315187	intron-variant	SCAP	GRCh38.p7	3:47454016	AACATATTAACAGAG[-/AT]ATCATCTCTGCCAAT	22937
rs557418981	snp	C/T	0.00119737	0.0244387	intron-variant	SCAP	GRCh38.p7	3:47445361	AAGCGATTCTCTTGC[C/T]TCAGCTTCCTGAGTA	22937
rs557427980	snp	C/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47470675	CAAGACTAGCCTGGC[C/G]AACATGGTGAAATCC	22937
rs557482656	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47421485	GGAACAATGAAGAGA[A/G]AGAGAGAGGGATTAA	22937
rs557596309	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47462131	AAATTATTAACATAA[A/C]CATCATTTTAACCCC	22937
rs557685380	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47470495	CTGGGCAAGAAGAAA[A/G]CCTGACAACTAGGCA	22937
rs557714020	snp	A/G			intron-variant, upstream-variant-2KB	SCAP, LOC105377073	GRCh38.p7	3:47475270	AGCCGGTTAAATACT[A/G]AGGTCATAAACCCAC	22937
rs557737198	snp	A/C	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47415499	ATTAAAAACAAGCAG[A/C]GGGCTCCATGTAGCC	22937
rs557737849	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47458233	GTCAGGAGTTCAAGA[C/T]CAGCTGGCCAACACA	22937
rs557755753	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47429709	CACTTCCAATTTTTA[C/T]TGAAGCACAGCCACA	22937
rs557800342	snp	A/G	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47455452	ATACAAAAATTAGCT[A/G]GGCATTGTGGCACGT	22937
rs557837143	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47454561	GTGAAACCCCCGTCT[C/T]CACTAAAAAATACAA	22937
rs557885880	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47423745	AGTACAGTCCAATGG[C/T]CCCATGGCTCCCCAG	22937
rs557885924	snp	G/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47416944	CCTAACGCTTTTAAT[G/T]GTTACCTTCCCATCC	22937
rs557923879	snp	C/T	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47422919	CAGCATGACAGTGTG[C/T]CCATCAACCACATGG	22937
rs557983281	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47426397	TTCTTTGTCTCCCTT[G/T]CCGGACCTACTCCAA	22937
rs558076851	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47446913	CACACCATTGCACTC[C/T]AGCCTGGGCAACAGA	22937
rs558214220	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47437558	CCAGCCTGGGCAACA[C/T]GGTGAAACGCCATCC	22937
rs558458280	snp	A/C/G	3.30038e-05	0.00406212	missense	SCAP	GRCh38.p7	3:47420942	CTACCTCCATCCGGC[A/C/G]AATGTCAATGGACAG	22937
rs558485701	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47455424	ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA	22937
rs558571920	snp	C/T	0.00119737	0.0244387	intron-variant	SCAP	GRCh38.p7	3:47453229	CCCACATGGTCAGCA[C/T]GGACAGCTTCCTAAA	22937
rs558772164	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47476011	CGTGCGCCCAGCGGC[A/G]TGCGCATGCGTAGTC	22937
rs558781415	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47477576	ACTCCGTCTCAAAAA[A/T]AAAAAGAAAAAAAAA	22937
rs558849594	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47428252	GTGGGTCATGAGTTA[A/G]CACAGTGGACACTGA	22937
rs558908336	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47478332	GAAGCATGGCAAACA[A/G]TCCTCCACTGCCCTA	22937
rs558928709	snp	A/C	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47441722	TTGAATTTGAACCCC[A/C]GTTTCCCTAATTATT	22937
rs558995462	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47460867	AGCAAGAACTCTTAA[C/T]ATAAACGTTGCATGG	22937
rs559039674	snp	C/T	0.00279162	0.0372561	upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47477746	AGGACTACAGATGAG[C/T]GCCACCATGCCATTT	22937
rs559120147	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47438510	TAATAAACTTGCTTT[C/T]ACTTAAAAAAAAGTT	22937
rs559126381	snp	A/G	0.000119345	0.00772387	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47425964	GCCCGTTTAGCTTGG[A/G]GAAAGCCCTCAGCCT	22937
rs559130192	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47478253	AGTGAAGTCTGGACA[C/T]TCCCCCACAAAAAAT	22937
rs559170487	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47461445	ACCACACAATTCTTC[C/T]AAATGTTCACAGTCA	22937
rs559204497	snp	C/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47420005	CTAAGCTCCACCTCA[C/G]CTGGAGCCAGAAAGC	22937
rs559208453	snp	A/C	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47420412	GGAGGACACAACGGG[A/C]AACTCCCCAGAGCCA	22937
rs559246426	snp	C/G	0.00159617	0.0282053	intron-variant	SCAP	GRCh38.p7	3:47468845	TTCTAGGGTTTTTAT[C/G]GTTTTAGGTCTAACA	22937
rs559320164	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47468407	ACTTTTTAATGATCC[C/T]CATTCTAACTGGTGT	22937
rs559355994	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant, nc-transcript-variant	SCAP, LOC105377073	GRCh38.p7	3:47476239	AGTCCAAGGCGCGAA[G/T]ATCGCTTGAGCCGAG	22937
rs559388310	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47454002	AACAATGTTATGTTC[A/G]ACATATTAACAGAGA	22937
rs559422169	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47477608	AGAAAGAAAGAATTT[G/T]TTAGGTTATTTTTAT	22937
rs559430262	snp	C/G	9.60061e-05	0.00692776	intron-variant	SCAP	GRCh38.p7	3:47427713	GTGTCTGCCACCACA[C/G]GGCAGACCTGCTGTA	22937
rs559499895	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47472489	ATAATAATAATTAAA[C/T]GAAGCTGAAATAAAC	22937
rs559530370	snp	A/G	1.78492e-05	0.00298735	intron-variant	SCAP	GRCh38.p7	3:47417274	CCGGGGCGGACAGCC[A/G]CTCTGCCCACCTTTA	22937
rs559552649	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47451961	CAGGGGCCTGGCACA[C/T]ACTGTTCCATCCTCT	22937
rs559562749	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47454701	TACAGTGAGCCAAGA[C/T]TGTGCCACTGCACTC	22937
rs559590334	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47430304	TTCTCACTAGAATCT[A/G]CCATCTACCTTTCAA	22937
rs559612800	snp	A/G			missense	SCAP	GRCh38.p7	3:47418734	GCCCAGCAGGTATGG[A/G]CCCCGGTGGGGGCCA	22937
rs559623764	snp	C/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47470165	ACAGGGGATCAAGAG[C/G]TAGCCTTAAGAGAAC	22937
rs559650722	snp	A/T			intron-variant	SCAP	GRCh38.p7	3:47423020	CCCACGCTATCACAC[A/T]GTCGCATGTCTAAGG	22937
rs559688178	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47459794	CTTAAACAACAGAAA[A/G]TAGGGTTCAAGAGCA	22937
rs559696771	snp	C/T	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47462569	CCATCCTGGCTAACA[C/T]GGTGAAACCCCGTCT	22937
rs559746982	snp	A/T	0.000798403	0.0199641	intron-variant, utr-variant-3-prime, downstream-variant-500B	PTPN23, SCAP	GRCh38.p7	3:47413720	GATGATATGGTTTTT[A/T]AAAAAAGTTTAATAT	22937
rs559857793	snp	C/T	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47441033	CAGCCTCCCGAGTGG[C/T]GGGGACTACAGGTGC	22937
rs560042918	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47434706	GTTGGGCGTGGTGGC[A/G]CACACCTACAGTCCC	22937
rs560148037	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47432420	CCCCCCTATGTCTCT[C/T]TGACATACACTATAT	22937
rs560268315	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47472307	GGCGCGGTGGCGGGC[A/G]CCTGTAGTCCCAGCT	22937
rs560343735	in-del	-/A	0.00199481	0.0315187	intron-variant	SCAP	GRCh38.p7	3:47457451	GGGAATAACTGAATC[-/A]CCTTGTGTTCCCTAG	22937
rs560381751	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47448275	TTCACATGTTCATTG[C/T]TAGTACATTGATTTT	22937
rs560409793	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47431236	TGGGCAGGGCCCACA[C/T]TCACTGTGCTGAGTG	22937
rs560457985	snp	G/T			intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47426467	TTTTTGAGACAAGAG[G/T]CTCGCTGTCGCCCAG	22937
rs560463193	snp	C/G	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47418911	TGCTGTGCTCGCCAG[C/G]CAGTCCTCTCCCTCC	22937
rs560555476	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant, nc-transcript-variant	SCAP, LOC105377073	GRCh38.p7	3:47476317	GTAAAATTAATTAGC[C/T]GGCTGTGGTGGCGCG	22937
rs560572255	in-del	-/GACTAGG	0.00279162	0.0372561	intron-variant	SCAP	GRCh38.p7	3:47438953	GCTGTGAAGGTAGAA[-/GACTAGG]GACTAGGAAGACAGT	22937
rs560589126	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47458875	CAACGGCGTGATCTC[A/G]GCTCACTGCAACCTC	22937
rs560601743	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47433956	CCAATGGCCAACCTG[A/G]GACATAAAGCCACAA	22937
rs560607975	snp	A/C/T	0.000168763	0.00918451	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47425639	GAGGGCGTATCAGGG[A/C/T]GGCCCCTCCCCCAGC	22937
rs560672392	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47448093	ATTTGCAAAGAACTG[C/G]CATGTTGAGTCTTCC	22937
rs560695936	snp	C/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47433222	AGTCCTTACCACCCA[C/G]TTCAGTATCGCTGGC	22937
rs560734967	snp	A/T	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47465611	CCATCTCTACAAAAA[A/T]TTTTTTAATTAGCCA	22937
rs560841317	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47439094	TAACGCTGTCGTAAA[C/T]TGAAAATATCCTAAG	22937
rs560863885	snp	G/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47468565	CTTTTTGATAGGGTT[G/T]TTTGATTTTTTTCTT	22937
rs561055207	snp	A/G	1.8257e-05	0.00302129	synonymous-codon	SCAP	GRCh38.p7	3:47419677	GGTCTGTGTATACCA[A/G]GATGCCAATCCAGAC	22937
rs561141890	snp	A/G	0.0267878	0.112589	intron-variant	SCAP	GRCh38.p7	3:47424695	GCAGACGGTATGGGG[A/G]AGGGTGGTGTTTAAC	22937
rs561178668	snp	C/T	0.000798403	0.0199641	utr-variant-5-prime, upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47475905	CCGCAGTCCGGTGCG[C/T]GGCGCCCTCCCTCTC	22937
rs561218612	snp	A/G/T	0.000165676	0.00910032	synonymous-codon	SCAP	GRCh38.p7	3:47418244	GCTGGCCAGGCACTC[A/G/T]ATGTCCTGCAGAAGC	22937
rs561227086	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47420195	TTTTGCCCAGCACTT[C/T]CCAGTGTCTGCACAC	22937
rs561238367	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47430093	GCACACACCACACAC[A/G]CATACAAACAGTGTC	22937
rs561238862	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	SCAP, LOC105377073	GRCh38.p7	3:47475168	GACTCACTGCCCCCC[C/T]CTCCGCATTCCCATC	22937
rs561275133	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47433724	ATACAAAAATTAGCC[A/G]GGTGTGGTGGCAACA	22937
rs561288444	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	SCAP, LOC105377073	GRCh38.p7	3:47474445	TGTGCTCAGTGGGAA[C/T]ACTGCAAATGTGTAA	22937
rs561350544	snp	A/G	0.00279162	0.0372561	intron-variant	SCAP	GRCh38.p7	3:47468203	ATGTGCCTTTATAGC[A/G]GCATGATTTATAATC	22937
rs561371921	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47463877	AGGGTCTTGCTCTGT[C/T]ACCCAGGCTGGATAC	22937
rs561396694	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47450455	TGCACAAAAGGAGAA[C/T]AGAGGGAAACGTTAG	22937
rs561492072	snp	C/T	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47466589	ACTGGGAAAACTGGA[C/T]AGTTACACGCAAAAG	22937
rs561579339	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47459741	AACTACTGATAAGGG[C/T]CTATGTTCAGCTGTG	22937
rs561606396	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47433407	CCGAGCCCTCTAGTT[A/G]TTCTGCACCAACACT	22937
rs561619946	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47443212	GCCTATATGCAAGGT[C/T]TAGTGACCTCAATCC	22937
rs561637744	snp	G/T	0.00914312	0.0669923	intron-variant	SCAP	GRCh38.p7	3:47449182	GCCTTTGGTATGCTG[G/T]TTAGGGTCAGATGCA	22937
rs561796480	snp	A/G	0.00318978	0.0398085	intron-variant	SCAP	GRCh38.p7	3:47437667	AGGATCGCTTGAGCC[A/G]GGAGGCTGAGGCTGC	22937
rs561862006	snp	A/T			intron-variant	SCAP	GRCh38.p7	3:47439532	TCTCTGACCTGCACA[A/T]AGGGCAGTCCAACTA	22937
rs561869282	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47464498	CATTACTAGAATGAA[A/G]GAGAAAAACAATGAT	22937
rs561885268	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47437123	GTTGAGGAACATTTG[A/G]CTGTTTCTGGTTTGA	22937
rs561915965	snp	G/T			intron-variant	SCAP	GRCh38.p7	3:47459917	CTTATCTCAACCGCA[G/T]AAGACAGACACTCCC	22937
rs561939888	in-del	-/A			intron-variant	SCAP	GRCh38.p7	3:47451015	CATGGCCAGCTAATT[-/A]AAAAAAAAAAAATGT	22937
rs561991763	snp	A/G	1.64925e-05	0.00287158	intron-variant, missense, utr-variant-5-prime	SCAP	GRCh38.p7	3:47428621	TGCCAGGGAAACACT[A/G]AGGACTTCACAAATA	22937
rs562057646	snp	A/T	0.00914312	0.0669923	intron-variant	SCAP	GRCh38.p7	3:47472448	TCCGTCTCAAAAAAA[A/T]AAAATAAAATAAAAT	22937
rs562092598	snp	C/T	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47445569	TTGTTTACTTGGTCT[C/T]GAACTCCAACTTTTT	22937
rs562139837	snp	A/C	0.00159617	0.0282053	intron-variant	SCAP	GRCh38.p7	3:47457757	CTAAAAATACAAAAA[A/C]TTAGCTGGGCCTGGT	22937
rs562161334	snp	C/G/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47421949	GGTCACTCTGGGCAA[C/G/T]GGGTGGTGGCCCTCC	22937
rs562185597	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47478876	CTCTCAGGTTCCAGC[A/G]ATTCCCGTGCCTCAA	22937
rs562253115	snp	C/T	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47448140	ATATTTTTCCATCTA[C/T]TTAGATCTTTGATTT	22937
rs562355737	snp	C/T	0.00676609	0.0577691	intron-variant	SCAP	GRCh38.p7	3:47422004	TGCGTCTGGCGACTG[C/T]GGCACAGGCCAGGGC	22937
rs562373263	snp	A/C	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47465356	TTGTATTGTTAGTAG[A/C]GACAGGGTTTCACCA	22937
rs562399272	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47416613	ACGTCACACCCCTAA[C/T]GCTTTTTTTTTTTTT	22937
rs562408698	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47466023	CTGTAATATCAACTA[C/T]TCAGGAGGCTGAGGC	22937
rs562426423	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47444255	CTGTTTTCTTCGGTC[C/T]GTGCTAGAGGGAACC	22937
rs562436228	snp	A/G	6.60884e-05	0.00574803	synonymous-codon	SCAP	GRCh38.p7	3:47422472	TAGGGTGAAGTAGCC[A/G]ATGAGGATGATGCCC	22937
rs562474785	snp	C/T	0.00318978	0.0398085	intron-variant	SCAP	GRCh38.p7	3:47447670	CTCCAGCCTGGGCAA[C/T]ACAGCGAGACTCTGA	22937
rs562479666	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47452330	GGAGTTTGATGCCAG[C/G]CTGGGCAACACAGTG	22937
rs562526395	snp	C/T	0.00557542	0.0525036	intron-variant	SCAP	GRCh38.p7	3:47440941	GGAGTCTCACTCTTT[C/T]GCCAGGCTAGAGTGC	22937
rs562562485	in-del	-/GCG/GCGGCG	0.0354911	0.128556	utr-variant-5-prime, intron-variant, upstream-variant-2KB	SCAP, LOC105377073	GRCh38.p7	3:47475829	TCCCAAGCTGCGGCG[-/GCG/GCGGCG]GCGGCGGCGGCGGCG	22937
rs562691716	in-del	-/C	0.131038	0.219882	intron-variant	SCAP	GRCh38.p7	3:47452926	GAGATCCTGTCTCTA[-/C]AAAAAAAAAAAAAAT	22937
rs562692017	snp	C/G	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47429344	AACGATGGCCTGTAG[C/G]CCAAATCAGGGCCCA	22937
rs562734628	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47424736	TCAGGAAAGGGAGCA[A/G]GTATCTAAGAGCAAC	22937
rs562886988	snp	A/G	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47437792	TTTAATTAAAAAAAA[A/G]AAAAAAAAAGAATAA	22937
rs562890844	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47438671	AAACAAAAATTGGCC[A/G]GACGCGGTGGCACAC	22937
rs563036746	snp	C/G	0.000154333	0.00878309	missense	SCAP	GRCh38.p7	3:47417462	ACAGCACCGGCCCAG[C/G]CGAGGGTGGGCGCAG	22937
rs563054053	snp	C/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47473436	GTAGCAAGTTCTAAC[C/G]GAAGGAGCTCAGGTG	22937
rs563054687	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47474121	ATACAAAAAAGTAGC[C/T]GGGCATGGTGGCGGG	22937
rs563090503	snp	C/T	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47470424	GGCTATAGTGAGATG[C/T]GGGACTGGTAAAAAG	22937
rs563157813	snp	G/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47421168	AGATGAGAGATGCTG[G/T]TTGGTCCTCAGCTCA	22937
rs563214306	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47464781	ACCTTCTCACTGCCT[C/T]ATTTACCCTTTCTCT	22937
rs563227475	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47473846	TAGTAATAAACTTGT[A/G]GTAAACTTTTTACCC	22937
rs563234429	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47448576	TTTTCATTTTATTTC[A/G]ATCTCTGTTGGTCAG	22937
rs563250460	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47478548	TGAGGTGTTGGCTCA[C/T]AGCAACCTCCCCCTC	22937
rs563294855	snp	A/G	0.00119737	0.0244387	intron-variant	SCAP	GRCh38.p7	3:47428355	CCACCGTAGACCCAC[A/G]AGGATGCTGAGAAAT	22937
rs563313871	snp	C/T	0.000112091	0.00748551	intron-variant	SCAP	GRCh38.p7	3:47435189	ATGAGAGGCAGTCCT[C/T]TCTCAGCACTGACAC	22937
rs563332028	snp	A/C	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47461085	TCCCCTCTGTACCCC[A/C]TCCATGCCCACCAGC	22937
rs563377468	snp	G/T	0.00159617	0.0282053	intron-variant	SCAP	GRCh38.p7	3:47460547	AAGAACTGTTTTTTG[G/T]TTTTTTGTTGTTGTT	22937
rs563392374	snp	C/T	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47415917	GTCAGGTTGAGACAT[C/T]GGGGCTTTCCTTAAA	22937
rs563406962	snp	G/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47421857	CTGGCATCAGTCTGG[G/T]GTTCCAGCTCAGTGC	22937
rs563414592	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47471314	AGTAATATTTAGAAC[A/G]GGAAGGAAATGTGTT	22937
rs563415733	snp	A/G	0.00119737	0.0244387	intron-variant	SCAP	GRCh38.p7	3:47453472	GCCTGCATATCTGAG[A/G]CCATACTTCTTTGCT	22937
rs563443818	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47445639	TGCAGCAGCGCGATC[C/T]CAGCTCACTGTAAAC	22937
rs563462946	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47463529	CAACATAGTGAAACC[C/T]TGTGTCTACTAAAAA	22937
rs563471822	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47416053	GGTGACAGGAATGAC[A/G]GCAGCAGCCCACTGG	22937
rs563507091	snp	A/C	0.0023933	0.0345097	intron-variant	SCAP	GRCh38.p7	3:47463748	AGAAAACAGGGGCTT[A/C]GCCTTGTTCACTGCT	22937
rs563508472	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47438738	AGAATCGCTTGAACC[C/T]GGGAGGTGGAGGTTG	22937
rs563585372	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47455688	AGAAAAACATGCCAC[A/G]TTCTTAATGAGGAAA	22937
rs563639796	snp	C/G	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47452747	GAGCCCAAGAGTTGC[C/G]TAAGTCAACTCTATG	22937
rs563669655	snp	G/T			upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47477163	CACTATTGTCACAAT[G/T]AAAGTAACAATGGGG	22937
rs563706156	snp	A/G	1.66294e-05	0.00288347	missense	SCAP	GRCh38.p7	3:47414241	CTGATGAGGTCATCC[A/G]GGCCACTGCTGATGA	22937
rs563730329	snp	A/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47469141	TCACTTGAGGTCAGG[A/T]GTTCAAGACCAGCCT	22937
rs563734388	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47472361	ATGGCGTAAACCCGG[A/G]AAGCGGAGCTTGCAG	22937
rs563783701	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47469501	TAGCTAGAATTACAG[A/G]TGCGTGCCACCATGA	22937
rs563789959	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47461208	AGTGCTATGGGTTCT[C/T]GTCAAGTCACAATGT	22937
rs563807434	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47447418	AAAAAGGCCAGGCGC[A/G]GTGGCTCACGCCTGT	22937
rs563894122	snp	A/C	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47444483	ATCCAGGAACCCTTT[A/C]TTTTTTTTGACATAG	22937
rs563921887	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47462760	CTCCGTCTCAAAAAA[A/G]AAAAAAAAAAAAAAG	22937
rs564006006	in-del	-/A			intron-variant	SCAP	GRCh38.p7	3:47429235	CCAAATCCTGGTGTC[-/A]ACAGTATTGGCTTCT	22937
rs564017528	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47414132	ACAAGCTCAGTCCTG[A/G]GTCCTTCCCTAAAAT	22937
rs564093037	snp	A/C	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47416091	CAACATCACTAAGGG[A/C]AAGGGACGCCCCCTC	22937
rs564106203	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47456960	GGGAGGCTGAGGCGG[A/G]TGGATCACCTGAGGT	22937
rs564204658	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47416531	AGAAAGGATAGGAGT[A/G]TATCACTCCCCACTG	22937
rs564251836	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47446481	TGGCCCCCCTCAATT[C/T]TTATGTTTACTTTTT	22937
rs564282970	snp	C/T	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47444635	TGCACCACCATGCCC[C/T]GCTAATTTTTGTATT	22937
rs564327195	snp	G/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47438969	GACTAGGAAGACAGT[G/T]AATAATAACAATGAA	22937
rs564415888	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47447387	GACAGACTGTGACTC[C/T]GTCTCAAAAAAGGAG	22937
rs564447391	in-del	-/A			intron-variant	SCAP	GRCh38.p7	3:47432316	AAGACTCCGTCTTGA[-/A]AAAAAAAAAAAAAAA	22937
rs564540502	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47427997	CCGGGGTAAATTAGG[A/G]GCTTCATTTAGTTCA	22937
rs564599656	snp	A/C/G	0.00159649	0.0282165	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47426835	TGCCCCACTGGGAAG[A/C/G]ACACAGGCCATATAG	22937
rs564671586	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47444418	GGAATGCCTATTGCT[C/T]GTTCTACCTTTCCGA	22937
rs564686093	snp	C/T	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47436951	GTCATATAAATGAAA[C/T]CATTCATTCTACTTA	22937
rs564729890	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47421917	ACAGCTGAGTGAGGG[C/T]ACTTTGCCAAGAGCA	22937
rs564763549	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47420243	ACCCGACCCAGGGCA[A/G]TGTGGTGGCCACAAG	22937
rs564785603	snp	C/T	0.0023933	0.0345097	intron-variant	SCAP	GRCh38.p7	3:47471966	ACCAATATGGTGAAA[C/T]CCCATCTCTACTAAA	22937
rs564926603	snp	A/G	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47469263	TGAGACAGAAGAATC[A/G]CTTGAACCGGGAGGC	22937
rs564994316	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, intron-variant, nc-transcript-variant	SCAP, LOC105377073	GRCh38.p7	3:47476363	CTACTCAGGAGGCTG[A/C]GGTAGGAGGATCACC	22937
rs565021533	snp	A/C	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47447028	TTTTTCCCCTTTGGT[A/C]TAAAGATAGCCAATT	22937
rs565036280	snp	C/T	0.0023933	0.0345097	intron-variant	SCAP	GRCh38.p7	3:47434635	CCAAGGTCAGGAGTT[C/T]GAGACCAGCTTGGCC	22937
rs565041040	snp	A/G	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47461128	TTCATCCTGCTCACC[A/G]CTGGCCCTAAGACTC	22937
rs565067857	snp	G/T	0.00318978	0.0398085	intron-variant	SCAP	GRCh38.p7	3:47414448	CTGTCAACAGTGGTG[G/T]CCCTGTGCCCCAGTG	22937
rs565087857	snp	A/G	0.000798403	0.0199641	utr-variant-5-prime, intron-variant, upstream-variant-2KB	SCAP, LOC105377073	GRCh38.p7	3:47475839	GCGGCGGCGGCGGCG[A/G]CGGCGACGGGGGCGG	22937
rs565298021	snp	C/T	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47425299	GCTAGATATGCTATA[C/T]ACAAACACAAGTATG	22937
rs565303881	snp	C/G	0.000798403	0.0199641	synonymous-codon	SCAP	GRCh38.p7	3:47418375	CTCGGGTGGCGCATA[C/G]CCGTAGTCGTCGCAG	22937
rs565352182	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	PTPN23, SCAP	GRCh38.p7	3:47413482	AGCTCCAGTAGCACT[A/G]CCAGGAACTTAACTT	22937
rs565367079	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47434344	ACCTGACAGGCAAAA[C/G]GTACACAGATGAGCT	22937
rs565410878	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47442799	AGGCCAAGGGCTCCA[C/T]AGTGGTTAGGGTTAG	22937
rs565467436	snp	C/T	0.000331532	0.0128707	downstream-variant-500B, synonymous-codon	PTPN23, SCAP	GRCh38.p7	3:47413866	CGCTCAGTCCAGCTT[C/T]TCCAGCACAGAGGGC	22937
rs565474471	snp	G/T	0.00159617	0.0282053	intron-variant	SCAP	GRCh38.p7	3:47450516	TATATGCAGGGTTTT[G/T]TTTTTTTTTTCCTTG	22937
rs565510070	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47459760	TGTTCAGCTGTGCAC[A/G]TATTGTCTTGATAAA	22937
rs565537329	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47443397	TCATGTGTGGCACAC[A/G]AAACCATGCCTGTGT	22937
rs565584820	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47451861	CTGCACAACCCACCC[C/T]GGTCCTCTGCAACTT	22937
rs565621081	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47462668	TGAGGCAGGAGAATC[A/G]CTTGAACCTGAGAGG	22937
rs565630371	snp	A/G	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47468824	AATGGTATTGCCTAG[A/G]TTTTCTTCTAGGGTT	22937
rs565639074	snp	A/C	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47444089	TTGCTTATGTTGGCC[A/C]AAGTTAATTTCTGGT	22937
rs565687173	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47419836	CACAGGCCCCACTGC[A/G]TCCTTTTCTCCTGCC	22937
rs565705426	in-del	-/CA			intron-variant	SCAP	GRCh38.p7	3:47456128	ATAAATTCCAAAAAG[-/CA]CAGTGGCTCAGGCCT	22937
rs565718259	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47476394	TGAGCCCGGGAGGTC[A/G]AGGCCACAGTGAGAC	22937
rs565737088	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47415506	ACAAGCAGAGGGCTC[C/T]ATGTAGCCTGGAGCT	22937
rs565811593	in-del	-/A	0.00358779	0.0422022	intron-variant	SCAP	GRCh38.p7	3:47454757	TCAAAAAATAATAAT[-/A]AAAAAAATACACATA	22937
rs565844441	snp	C/T	3.36978e-05	0.0041046	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47425977	GGAGAAAGCCCTCAG[C/T]CTCCCTGCCATGAAC	22937
rs565855743	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47452957	TTAAATTAGCCAATT[A/G]TGGTGGCTCATGACT	22937
rs565903936	snp	A/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47461212	CTATGGGTTCTTGTC[A/T]AGTCACAATGTGTGA	22937
rs565923370	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47449535	CTACACAATTACGTG[A/G]AGGGCCAGAGCAAGA	22937
rs565957903	snp	A/C/G	1.65463e-05	0.00287626	intron-variant	SCAP	GRCh38.p7	3:47421049	AATCAGAGCACATGG[A/C/G]GATGGGGGGGTGCCG	22937
rs566142306	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47442425	ACACAAGAAAATGAC[C/T]AGAGAGCAAAGAAGC	22937
rs566144319	snp	A/G	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47432829	TGCACCACTGCACCC[A/G]GCCCTATTGTCCCTT	22937
rs566181298	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47441258	GAAACCATAGTACCA[C/T]CAGAGAGTAAAACCA	22937
rs566198681	snp	C/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47419272	CCTGCATTGGGGAAA[C/G]GGGATGGTGAGTTGA	22937
rs566252553	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47433471	AAACACATCACACCC[C/T]TTACGGCCTCATCAT	22937
rs566292750	snp	A/C	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, upstream-variant-2KB	SCAP, LOC105377073	GRCh38.p7	3:47475490	AACAGCTTCCCGGAG[A/C]AACTAGGCCAGGGGA	22937
rs566292824	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47466089	AGTGAGCCAAGATTG[C/T]GTCACTGCACTCCAG	22937
rs566318431	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47426509	GTGGCGCCATCTGGG[A/C]TCACTGCAAGCTCCG	22937
rs566352457	snp	A/C	0.000798403	0.0199641	upstream-variant-2KB, utr-variant-5-prime, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47476037	TAGTCGAACCACATT[A/C]GCGTCTCCCGTTCGC	22937
rs566438733	snp	A/G	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47430801	GCAGGGCCCAGCCCA[A/G]CTGAGGGATGAGGGG	22937
rs566540878	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47416326	CGGAGTACTGGGGAC[A/G]CCCACAGCCAACAGG	22937
rs566605396	snp	C/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47423777	GCACACACTCAAGAG[C/G]TGCCAGGGCCCAGTG	22937
rs566619829	in-del	-/T	0.00119737	0.0244387	intron-variant	SCAP	GRCh38.p7	3:47416793	ACTACGCCCGGCTAA[-/T]TTTTTTGTATTTTTA	22937
rs566650663	snp	C/T	0.00171289	0.0292149	intron-variant, synonymous-codon, utr-variant-5-prime	SCAP	GRCh38.p7	3:47428545	GTTCCGGATCTCCTC[C/T]ACCAGTTGGAATGCC	22937
rs566652349	snp	A/G	0.00159617	0.0282053	intron-variant	SCAP	GRCh38.p7	3:47416788	CCCGCCACTACGCCC[A/G]GCTAATTTTTTGTAT	22937
rs566686755	snp	A/G	3.69317e-05	0.00429703	missense	SCAP	GRCh38.p7	3:47417708	GGCCCCGGGGGCGGT[A/G]TCTCAGGGGAGGGCT	22937
rs566712949	snp	A/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47446988	TGAGTTAATTTTTAG[A/T]TAAGGTGTGAGATAT	22937
rs566737515	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47456637	CAGTGTGGTGGTACA[C/T]GCCTGTAGTCTCAGC	22937
rs566787075	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47439203	TACTTGAGGTCAGGA[A/G]TTTGACACCAGTCTG	22937
rs566797657	snp	C/T	7.46798e-05	0.00611018	missense	SCAP	GRCh38.p7	3:47418403	CAGGGCAGCTCCCCG[C/T]GCCTCCGCCGCCCGG	22937
rs566809194	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47429006	CCCGGAATTTGCACA[C/T]GGGACCTGTGAGGTG	22937
rs566832404	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47472828	GCTCACGCCTGTAAT[C/T]CCAGCACTTTGGGAG	22937
rs566943105	snp	A/C	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47457410	CTCTCAGCCTCCTGG[A/C]TTGACTGCGTTCCCC	22937
rs566979318	in-del	-/A	0.0023933	0.0345097	intron-variant	SCAP	GRCh38.p7	3:47472277	CTCTACTAAAAATAC[-/A]AAAAAAATTAGCCGG	22937
rs566987823	snp	C/T	0.00119737	0.0244387	intron-variant	SCAP	GRCh38.p7	3:47464847	ATTTCCGTTCCTAGA[C/T]GACATGATCTTACAT	22937
rs567038356	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47445815	GACCTTAGATGATTT[C/G]CCAGCCTGGCCTCCC	22937
rs567068047	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47424852	ATTAATAACCATTAA[C/T]AGACAGGCAGGCGGG	22937
rs567076032	snp	A/G	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47467759	CCCACTGGCCCTTGG[A/G]TACATGTGCACAACA	22937
rs567080380	snp	G/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47459442	CCCACCCCCAATATT[G/T]CAACATAGGTTCTTT	22937
rs567080907	snp	C/T	0.00119737	0.0244387	intron-variant	SCAP	GRCh38.p7	3:47456747	GTGAGATCGTGCCAC[C/T]GTACTCTAGTCTGGG	22937
rs567146049	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47441327	ACGAAAAACAGCCAA[C/G]TGTGGTGGCGCACAC	22937
rs567165119	snp	A/G	0.29046	0.246704	intron-variant	SCAP	GRCh38.p7	3:47467099	CTCTGTCTTAAAAAA[A/G]AAAAAAAAAAAAAAG	22937
rs567219264	snp	G/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	SCAP, LOC105377073	GRCh38.p7	3:47474882	AGACACCCTCGACCC[G/T]GACTCCCTAATAAAA	22937
rs567235689	snp	C/G	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47424549	AGCTCTACCAGCTAT[C/G]TGAGCCCACTGTCCC	22937
rs567401477	snp	A/C	0.000833097	0.0203925	missense	SCAP	GRCh38.p7	3:47417818	ACGCCACTGTCCCGG[A/C]GCTGCCTGCTGGGGG	22937
rs567518732	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47439397	CTGGGCGACAGAGTG[A/G]GACCCCGTCTCAAAA	22937
rs567568203	snp	C/G	0.000265965	0.0115287	intron-variant	SCAP	GRCh38.p7	3:47417269	AATCCCCGGGGCGGA[C/G]AGCCGCTCTGCCCAC	22937
rs567583225	snp	A/T	0.00119737	0.0244387	utr-variant-3-prime, downstream-variant-500B	PTPN23, SCAP	GRCh38.p7	3:47413275	TCTCAGTGGGCACAG[A/T]CTCTTACTCCCATTT	22937
rs567592381	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47473705	GGCTAGATTCTGAGA[A/G]AGAAAACATCCCTAA	22937
rs567752832	snp	G/T	0.00119737	0.0244387	intron-variant	SCAP	GRCh38.p7	3:47424737	CAGGAAAGGGAGCAG[G/T]TATCTAAGAGCAACG	22937
rs567876749	snp	G/T	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47440291	CTCTGGAAGAAGGGG[G/T]CACTGCTCTGCTGCT	22937
rs568047542	snp	C/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47446010	CCTCCTGAGTAGCTG[C/G]AATTACAGATGCGCG	22937
rs568074921	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47446654	ATTTGTTTAAGTCTG[C/T]AATCCAGCTGGGTGC	22937
rs568091891	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47436009	AGCCATGATTATACC[A/G]CTGCACTCCAGCCTG	22937
rs568135188	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47429014	TTGCACATGGGACCT[A/G]TGAGGTGGCATCAAG	22937
rs568135196	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47437941	CCAAACAGTTTTCCA[C/T]AGCGGTTGTACAAAT	22937
rs568162949	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47453705	CCAGAGGTGTAATAC[A/G]CCCCCATGTTACCCA	22937
rs568245405	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47429568	TTGCCAGGCTGGTCT[C/T]GAACTCCTGGGCTCA	22937
rs568266289	snp	G/T	0.00199481	0.0315187	intron-variant	SCAP	GRCh38.p7	3:47462295	TTTACTATATAACTT[G/T]TCAAAGGTTTTTCTG	22937
rs568302960	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47416836	TTTCACCGTTTTAGC[C/T]GGGATGGTCTCGATC	22937
rs568341574	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47458864	AGGCTGACGTGCAAC[A/G]GCGTGATCTCGGCTC	22937
rs568355260	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47470614	ACGCCTATAATCCCA[A/G]CACTTTGGGAGGCCG	22937
rs568389778	snp	A/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47422720	CTTTAAGGGGCCATC[A/T]CCACCACACAGCTGC	22937
rs568503695	snp	C/T	5.09836e-05	0.00504868	intron-variant	SCAP	GRCh38.p7	3:47420823	CATCCAGAGGCTGCT[C/T]GCACAGGACCGCTGT	22937
rs568506498	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47447595	TGGGAGGCGGAGACA[A/G]GAGAATTGCTTAAAC	22937
rs568580356	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47428050	TAGCTAACTAAAACC[C/T]GGCAGTGATGCAGCT	22937
rs568682671	snp	C/T	0.00119737	0.0244387	intron-variant	SCAP	GRCh38.p7	3:47454292	GAATGGTGTGAACCC[C/T]GGGGGACGGAGCCTG	22937
rs568778060	in-del	-/A			intron-variant	SCAP	GRCh38.p7	3:47448033	AAAAAAAAAAAAAAA[-/A]CTTGATAGAATTTTG	22937
rs568830654	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47430766	GACAGCGGTGTACTG[C/T]GAGGTGTGGACTGAA	22937
rs568832199	snp	C/T	0.00398564	0.0444627	intron-variant	SCAP	GRCh38.p7	3:47438024	TGTCACCTCTTGATA[C/T]TGTCAGTCCAATTAA	22937
rs569006408	in-del	-/CA	0.00119737	0.0244387	intron-variant	SCAP	GRCh38.p7	3:47461453	ATTCTTCCAAATGTT[-/CA]CAGTCACTTCTCAGA	22937
rs569059149	snp	C/T	0.00119737	0.0244387	intron-variant	SCAP	GRCh38.p7	3:47421998	AGGCCATGCGTCTGG[C/T]GACTGCGGCACAGGC	22937
rs569059762	snp	C/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47423727	ACACATGAACCAGGA[C/G]GAAGTACAGTCCAAT	22937
rs569135423	snp	A/G	1.89439e-05	0.00307759	synonymous-codon	SCAP	GRCh38.p7	3:47417667	GGTGAGGTCAGGCTG[A/G]TCCCCGAAGAGGGAA	22937
rs569151392	snp	C/T	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47463179	TGTTTATTCCTCCGG[C/T]GGAAAGTTTAGGAAA	22937
rs569152411	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47464951	ACATGCAAAAATCAG[C/T]TGCATTTCTATTGTT	22937
rs569182439	snp	A/C	1.80628e-05	0.00300517	intron-variant	SCAP	GRCh38.p7	3:47417285	AGCCGCTCTGCCCAC[A/C]TTTAGCCCCTCTGCC	22937
rs569192252	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47458488	TTTCAGTTAATGAAC[A/G]AAAGCTGATTTCAGA	22937
rs569222886	snp	A/G	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47424336	GGAGAGCTGTGCAGC[A/G]CCACTGCTAGACCAC	22937
rs569266245	snp	A/T			intron-variant	SCAP	GRCh38.p7	3:47465856	CAAAAAAAAAAAAGC[A/T]GGGTGCAGTGGCCCA	22937
rs569299971	snp	C/T	0.0023933	0.0345097	upstream-variant-2KB, intron-variant, nc-transcript-variant	SCAP, LOC105377073	GRCh38.p7	3:47476228	AACACTGTGGGAGTC[C/T]AAGGCGCGAAGATCG	22937
rs569308130	snp	C/T	0.00159617	0.0282053	intron-variant	SCAP	GRCh38.p7	3:47463969	CTCACACTGCTGGGA[C/T]TACAGGCATGAGCCA	22937
rs569370540	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47416731	TCCCGGGTTCACGCC[A/G]TTCTCCTGCCTCAGC	22937
rs569393765	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47472643	CCCTTGACTGCTTAA[A/G]CAGAAACTGTCAAAT	22937
rs569425836	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47441102	AGACGAGGTTTCACC[A/G]TGTTGGCCAGGATGG	22937
rs569479317	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47440237	AAACTACTAGAAGCA[A/G]TCTATATCCATACTT	22937
rs569584010	snp	C/T	0.00199481	0.0315187	intron-variant	SCAP	GRCh38.p7	3:47428198	TCGGCAGAGACACCA[C/T]CATTACATTCACACC	22937
rs569653244	in-del	-/AT			intron-variant	SCAP	GRCh38.p7	3:47467671	AAATGGCCAATCAAC[-/AT]ATGAAAAATTGCTCA	22937
rs569676196	snp	A/C	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47469444	CTGGCTCACTGCAAC[A/C]TTTACCTCTGGGTCC	22937
rs569712814	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47460808	TGATCCACCCGCCTC[A/G]ACCTCCCAAAGTGCT	22937
rs569784862	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47444221	CCAAGTTTAAACCTA[C/T]TTCTCTTGTTCCATG	22937
rs569788469	snp	C/G	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47453145	TCCAAAACCACCAGC[C/G]TGAAAAATTCTAATA	22937
rs569819873	snp	G/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47437170	TTGGGCCAGGCACAG[G/T]GGCTCACGCCTGTAA	22937
rs569899239	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47454174	AGATTGAGACCATCC[C/T]GGCTAACACAGTGAA	22937
rs569915522	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47430974	AATGCCTCCTGGGAC[C/T]CTGGGCACAAAGGAA	22937
rs569940061	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47436239	GACCATGAAAATTAT[A/G]TATAATTAACTAAGG	22937
rs570007518	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47419045	CCCAGATACCAGCAC[C/G]CAAACAGCCCTGGTG	22937
rs570118924	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant, nc-transcript-variant	SCAP, LOC105377073	GRCh38.p7	3:47476690	TCGCATTTGGCCCTC[C/T]TGAAAATCCGAGGTA	22937
rs570134676	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47425850	AAGCTCCTAAGACCC[C/T]GCTGGGGGACAAAGC	22937
rs570140804	snp	C/T	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47434131	TGCCTCTATTTCAGC[C/T]GCAGAGTCAAGTTCA	22937
rs570174501	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47433589	AGGTTAATGAAGTCC[A/G]GACACAATGGCTCAC	22937
rs570212243	snp	G/T	0.000280994	0.0118498	missense	SCAP	GRCh38.p7	3:47414000	AGACTGTCTGTAACA[G/T]GTCCCCGTAGTTTAG	22937
rs570307297	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47477349	AGATCATGAGGTCAG[A/G]AGATCGAAACCATCC	22937
rs570365226	snp	A/G	0.00398564	0.0444627	intron-variant	SCAP	GRCh38.p7	3:47422018	GCGGCACAGGCCAGG[A/G]CCAAGGGAGGAGACC	22937
rs570452946	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47454223	ATACAAAAAATTAGC[C/T]GGGCGAGGTGGCGGG	22937
rs570462292	snp	A/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47462209	CAGCCATCACCACCA[A/T]CCATCTTTTTTATCT	22937
rs570492461	snp	C/T	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47443944	TATTCATGATGTTTA[C/T]TCATCCCACAGAGGT	22937
rs570528484	snp	A/G	0.0023933	0.0345097	intron-variant	SCAP	GRCh38.p7	3:47445808	AACTCCTGACCTTAG[A/G]TGATTTGCCAGCCTG	22937
rs570567060	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47445196	TGAATAGTGCTGTGA[C/T]GAACATTCTAACATT	22937
rs570604300	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47458220	GGTGGATCACGAGGT[C/G]AGGAGTTCAAGACCA	22937
rs570606204	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47437296	AATTCAAAATTAGCC[A/G]GGCGTGGTGGCGTAT	22937
rs570608838	snp	C/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47429471	AGCACCCCCACCCAC[C/G]AAGTAGCTGAGACTA	22937
rs570682265	snp	G/T			intron-variant	SCAP	GRCh38.p7	3:47444445	CCGAAAGCAGAAGCG[G/T]TAAGCGCACATGCAA	22937
rs570686632	snp	C/G	0.00119737	0.0244387	intron-variant	SCAP	GRCh38.p7	3:47461253	ATAAACAAATCACAT[C/G]TACATGGTGCTCATT	22937
rs570735558	snp	C/T	0.0023933	0.0345097	intron-variant	SCAP	GRCh38.p7	3:47434280	TCAGCAAGTCCAGCA[C/T]GAATCCAGGGACCAC	22937
rs570759071	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47477415	TACAAAACAAACAAA[A/C]AAAAAATTAGCCGGG	22937
rs570873024	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47446184	GGCCAACCTTTTTTT[C/T]TTTTTTTGAGATGGA	22937
rs570896201	snp	C/T	8.69112e-05	0.00659151	synonymous-codon	SCAP	GRCh38.p7	3:47418504	GACGATGCCGGTGGC[C/T]AGGCCCAGCGCCGCC	22937
rs570896213	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47425675	GCCCACTGGGGCTCC[C/T]GGGAGTAGGTTGCCC	22937
rs570917323	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47469505	TAGAATTACAGGTGC[A/G]TGCCACCATGACCCT	22937
rs570964994	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47434788	GTTGCAGTGAGCCGA[A/G]ATTGTGCCATTGCAC	22937
rs571056407	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47419231	GAACTGTTTTAATTA[C/T]TTGCATAATTCAAAC	22937
rs571101163	snp	A/T	0.00159617	0.0282053	intron-variant	SCAP	GRCh38.p7	3:47451358	AAGTAAAAATATACA[A/T]GTTTATATTCAAATA	22937
rs571120376	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47439276	TAGCCGGACGTGGTG[A/G]CTCACACCTGTAATC	22937
rs571120477	snp	C/G	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47415240	CAGCCCTGGGGCTGA[C/G]CATGTGGACATGAGA	22937
rs571173882	snp	A/G	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47443154	CACACTAGGGCTGCT[A/G]GAGGGAGGCGATAGT	22937
rs571187777	snp	A/T	1.66255e-05	0.00288314	intron-variant	SCAP	GRCh38.p7	3:47414693	CTGGTCTCTGGGATT[A/T]TCCAAGTTATACTTT	22937
rs571209947	snp	A/C	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47421193	AGCTCACATACCAGC[A/C]GCAGCTCACCCCGTC	22937
rs571217216	snp	A/G	0.00398564	0.0444627	utr-variant-3-prime, downstream-variant-500B	PTPN23, SCAP	GRCh38.p7	3:47413389	TTTATGGGACCCGAC[A/G]TTTTTCAGCTCTTTG	22937
rs571221424	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, utr-variant-5-prime, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47475979	ACCTTTACCCTCCCG[C/T]CCCGCCGCCCTCCGC	22937
rs571275288	snp	C/T	0.0023933	0.0345097	intron-variant	SCAP	GRCh38.p7	3:47467879	ATCCCTCCCCCCTCC[C/T]CCCATCCCCCGGCAG	22937
rs571305080	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47435787	GGCGCAGTGGGTTAT[A/G]CCTGTAACCCCAGCA	22937
rs571309652	snp	A/C	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	SCAP, LOC105377073	GRCh38.p7	3:47475601	GTGCAGGGACACGGC[A/C]GGGTTGGGGGTGGGG	22937
rs571412723	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47460622	CAGTGGCACAATCTC[A/G]GCTCACTGCAACCTC	22937
rs571443802	snp	C/T	3.44127e-05	0.00414791	intron-variant, utr-variant-3-prime, downstream-variant-500B	PTPN23, SCAP	GRCh38.p7	3:47413806	GGTTCAGTGCATTGG[C/T]CCCCACACAGCACCC	22937
rs571581075	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47425031	TAAAATGACCTATTT[C/T]ATTAGGCATTTAAAT	22937
rs571583594	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47465931	TGAGGTCAAGAGATC[A/G]AGACCATCTTGGCCA	22937
rs571661807	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47458170	AGGCGCAGTGGCTCA[C/T]GCCTGTAATCCCAGC	22937
rs571744339	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47441147	CCTCGTGATCTGCCC[A/G]CCTCGGCCTCCCAAA	22937
rs571773829	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47448394	TGGAAATTTCTACGT[A/G]GACTTATCATGTTAT	22937
rs571775627	snp	C/T	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47459051	CTCAGGTGATCTGCC[C/T]GCCTTGGCCTCCCAA	22937
rs571906633	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47433820	GTTGCAATGAGCTGA[A/G]ATCACGCCACTGTAC	22937
rs571966566	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47459312	TTTGCCTGATTTCCT[C/G]CAAGAAGCGTGCTTT	22937
rs572019069	snp	G/T	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47434463	TCTCATTTATATCAG[G/T]GTTCGGCCCAGAGAC	22937
rs572068868	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47456697	TTGAACCTGGGAGGC[A/G]GAGGTTGCAGTGAGC	22937
rs572109189	in-del	-/A	0.0023933	0.0345097	upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47477412	AAATACAAAACAAAC[-/A]AAAAAAAAATTAGCC	22937
rs572131220	snp	A/C	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47451611	ACCATGTTGCCCAGG[A/C]TGGTCTTAAACTCTT	22937
rs572217760	snp	A/G	5.23209e-05	0.00511446	synonymous-codon	SCAP	GRCh38.p7	3:47419611	GGGCTCCCTCACCCA[A/G]TGGGCTCTGTTCCGT	22937
rs572284118	snp	C/T	0.00104185	0.0228	synonymous-codon	SCAP	GRCh38.p7	3:47418172	GCAATCCCCGGTCTG[C/T]GCGTCCCACACGCAG	22937
rs572395450	snp	A/C	0.00119737	0.0244387	intron-variant	SCAP	GRCh38.p7	3:47431312	GTACGTGAATTTTTA[A/C]ATAATTTAGGAGGCT	22937
rs572415688	snp	C/T	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47424678	GCCCTGTGAAGGGTA[C/T]GGCAGACGGTATGGG	22937
rs572450847	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47431921	TATTGTCATCCATTC[A/G]TTTATTTATATTTAT	22937
rs572461776	snp	C/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47440759	CAACTACTCAGAGGG[C/G]TGAGGTAGGAGAATC	22937
rs572468674	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47473138	AACAGCATAAAAGGA[C/T]GGACTCTTTTGTCAG	22937
rs572498526	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47448503	GAGACTTCAAAAACA[C/T]AAAAGATAAACTTTC	22937
rs572500244	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47439582	TTTTTATCCCATGGC[A/G]CACCCACTGCTTACC	22937
rs572545256	in-del	-/TTT	0.00199481	0.0315187	intron-variant	SCAP	GRCh38.p7	3:47450512	TGATTATATGCAGGG[-/TTT]TTTTTTTTTTTTCCT	22937
rs572580395	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47474022	TGTAATCCCAGCACT[C/T]TGGGAGGCCGAAGCG	22937
rs572654691	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47446905	GCTATGACCACACCA[C/T]TGCACTCTAGCCTGG	22937
rs572680589	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	SCAP, LOC105377073	GRCh38.p7	3:47475165	AGCGACTCACTGCCC[C/G]CCCCTCCGCATTCCC	22937
rs572730737	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47422948	GGCAGAAGCACTCGG[C/T]GGGTAGAGGACCTGG	22937
rs572754270	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47467434	ACATGGTGAAACCCC[A/G]TCTCCACAAAAAATA	22937
rs572912925	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47457673	AGCACTTTGGGAGGC[C/T]GAGGTGGGTGGGTCA	22937
rs572929703	snp	A/C/G	0.000235859	0.0108573	synonymous-codon	SCAP	GRCh38.p7	3:47417394	ACTGGGGGCCCAGGC[A/C/G]AGGGAAGGGGAGCCT	22937
rs572991893	snp	C/T	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47465109	GAAACAAATTAAAGA[C/T]GTAAAATAAAGGGAA	22937
rs573010958	snp	C/T	0.000181631	0.00952797	utr-variant-5-prime, missense	SCAP	GRCh38.p7	3:47442956	TGGTTGTAGAAGGCC[C/T]GAGATATCTTCTCAC	22937
rs573018779	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47416963	ACCTTCCCATCCAAG[C/T]GGACTGCCCTCTGCT	22937
rs573042651	snp	G/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47456974	GGTGGATCACCTGAG[G/T]TCAGGAGTTCAGACC	22937
rs573106239	snp	C/G			utr-variant-5-prime, upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47475954	CCCGCCCCTTCACCT[C/G]TCACCTCCTACCTTT	22937
rs573127100	snp	A/G	0.00119737	0.0244387	intron-variant	SCAP	GRCh38.p7	3:47446121	CCTCGTGATCTGACC[A/G]CCTCAGCCTCCCAAA	22937
rs573198025	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47447873	AGCCGGGCATGGTGG[C/T]GTGTGCCTGTAATCC	22937
rs573200551	snp	C/T	0.00199481	0.0315187	intron-variant	SCAP	GRCh38.p7	3:47438485	GCCATTCTTTATTCC[C/T]TTACTTTTCTAATAA	22937
rs573202430	in-del	-/A	0.00159617	0.0282053	intron-variant	SCAP	GRCh38.p7	3:47454211	CTCTACTAAAAATAC[-/A]AAAAAATTAGCCGGG	22937
rs573226342	in-del	-/A			intron-variant	SCAP	GRCh38.p7	3:47433877	CCATCTCAAAACAAT[-/A]AAAAAAAAATGGTTA	22937
rs573238299	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47462483	TATGACTTATGATCA[A/G]ACACCATCAGAGGCA	22937
rs573268077	snp	A/C	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47465280	GGTTCAAGCGATTCT[A/C]CTGTATCAGCCTCCT	22937
rs573269861	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47455457	AAAATTAGCTGGGCA[C/T]TGTGGCACGTTCCTG	22937
rs573382341	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47428184	GAGCTTGCTTCTCGT[C/T]GGCAGAGACACCACC	22937
rs573389217	snp	A/T			intron-variant	SCAP	GRCh38.p7	3:47472132	TCCATCTCAAAAAAA[A/T]AATAATAATAATTAA	22937
rs573450932	snp	A/G	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47422189	GAGGGGTAGGAAGAC[A/G]GGGTCAAGGGCAGAG	22937
rs573482964	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47429266	AGCACATTGGGCAGC[A/G]AGCCTCTTTTGCTCA	22937
rs573539484	snp	C/T	0.00659138	0.0570285	missense	SCAP	GRCh38.p7	3:47417441	CCTCGTCCTCAGGGG[C/T]CTGGGACAGCACCGG	22937
rs573713819	snp	G/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47448719	AAATAAATTTCTGAT[G/T]TTCTGTTCATTTCAA	22937
rs573823528	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47447974	AGTGCCACTGCACTC[C/T]AGCCTGGGCAAGAGG	22937
rs573846928	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47462705	TTGCAGTGAGCCAAG[A/G]TCGCGCCATTGCACC	22937
rs573872197	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47440841	CTCCAGCCTGAGCAA[C/T]GGAAGCGAGACCCTG	22937
rs573937602	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47446334	ACTCACCACCACACC[C/T]GGCTAATTTTTTATT	22937
rs574005781	snp	C/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47430998	AAAGGAACAACCAGA[C/G]GCAACCGTCTGAGCC	22937
rs574221408	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47423819	ATTATGCCGGAGGCA[A/G]GAGCAAGGGACATTT	22937
rs574383880	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47445313	GTGCTGTGGCACAAT[C/T]TCCACTCAATGCAAC	22937
rs574424909	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47415330	CCAGAACAGATGCTG[A/G]AGCCAGAGGGCAACT	22937
rs574484847	snp	C/T	0.00119737	0.0244387	intron-variant	SCAP	GRCh38.p7	3:47427745	TTAGGGGACATCCTC[C/T]GTCTGTTCTTCAATG	22937
rs574504590	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47424780	ACAAAATACGACGTC[A/G]CTTTTCATACGACCA	22937
rs574511730	in-del	-/A	0.00159617	0.0282053	intron-variant	SCAP	GRCh38.p7	3:47421299	TCTTCCGGTCCCTCT[-/A]AGAGGGGACTGAAGG	22937
rs574527907	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47456063	AAGGTGTTGCAACAA[A/G]TGGGTAGCCACGGAA	22937
rs574531016	snp	C/T	0.0023933	0.0345097	intron-variant	SCAP	GRCh38.p7	3:47422053	GAAGGGTCTAGGAAC[C/T]CCACGGTGCTTCTCC	22937
rs574542593	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47416483	TCAATATTGACAAGC[C/T]AATCAGAGAAACTGG	22937
rs574559204	snp	A/G	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47415616	AAGCAGCTTCAACCC[A/G]AGCACAGCTCACATC	22937
rs574568988	snp	A/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47469850	GACTCCATTTTGATC[A/T]TAGTGCAAAGAGAGC	22937
rs574570949	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47446743	ACCAGGAGTTTGAGA[C/G]CAGCCTGGACACTGT	22937
rs574576628	snp	A/C	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47461048	ACCGGCCCCTTCCAC[A/C]ACCTTATCTCCCAGG	22937
rs574596002	snp	A/G	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47428345	CGGAATGCAGCCACC[A/G]TAGACCCACAAGGAT	22937
rs574687608	snp	A/C	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47471182	CCTTACAAATTTTAG[A/C]AAAAATGAGTACAGA	22937
rs574689740	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47416397	GAGAACAGCTGCCAG[C/T]GGCCAAGGAGAAGAG	22937
rs574755372	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47420167	AGGCCAGCCCAGCCC[A/G]GCTGGTGAATGATTT	22937
rs574763827	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47463442	TGCGGTGGCTCGTGC[C/T]TGTAATCCCAGCACT	22937
rs574819369	snp	C/T	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47437777	GGCTGGATAATTGTT[C/T]TTAATTAAAAAAAAG	22937
rs574905035	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47478621	GGGATTATAGGTGTG[C/T]GCCACCATGCCTGGC	22937
rs574937707	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47453360	CCAGTCTGGGCAACA[C/T]AGTGAGACCCCATCT	22937
rs574982069	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47452676	TCTCTATTTAACACA[C/T]CCTCCAGCTGACAGT	22937
rs575099655	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47444449	AAGCAGAAGCGTTAA[A/G]CGCACATGCAAGTTT	22937
rs575138913	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47443163	GCTGCTGGAGGGAGG[C/T]GATAGTTATGTGGCT	22937
rs575164706	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47437378	GGTGAGCTGAGATGG[C/T]GCCACTGCACTCTAG	22937
rs575171260	snp	C/T	0.00398564	0.0444627	intron-variant	SCAP	GRCh38.p7	3:47469339	GTGACAAGGAGACTC[C/T]GTCTCAAAAAAAAAA	22937
rs575195170	snp	A/C/T	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47461840	GGAGTTTGAGACCAG[A/C/T]GTGAGCAACACGGTG	22937
rs575272865	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47416512	GGCTTCATTGAGAAG[A/G]GCGAGAAAGGATAGG	22937
rs575280858	snp	C/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47472205	TTGGGAGGCCGAGGC[C/G]AGTGGATCATGAGGT	22937
rs575289421	snp	G/T	0.00358779	0.0422022	intron-variant	SCAP	GRCh38.p7	3:47421870	GGGGTTCCAGCTCAG[G/T]GCAGGGCCACCTCCA	22937
rs575330881	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47416878	TGATCCGCCCGCCTC[A/G]GCCTCCCAAAGTGCT	22937
rs575351519	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47453520	CAAAATATACTGAAA[C/T]CTCTTTCCAGCTTTA	22937
rs575384007	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47422774	CTGGAGGGTGCAGAG[A/G]AGAGCTATAATCATC	22937
rs575395331	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47473055	ATTGCACTCCAGCCT[A/G]GGCAAGAAGAGCGAA	22937
rs575442487	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47463565	AAATTAGCTGGGTGT[A/G]GTAGTGCCTGTAATC	22937
rs575463756	snp	A/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47455695	CATGCCACATTCTTA[A/T]TGAGGAAAAGTCAAT	22937
rs575504503	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47429643	ACTTCTTTATTTTCT[A/G]TAGAGATGGGGTCTC	22937
rs575572122	snp	C/T	0.0236746	0.106192	intron-variant	SCAP	GRCh38.p7	3:47436038	TGGGCAACATAAGAC[C/T]CCTGTCTCTGAAAGA	22937
rs575753498	snp	A/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47433960	TGGCCAACCTGGGAC[A/T]TAAAGCCACAAAACT	22937
rs575779776	snp	C/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47444527	CGACCAGGCTGGAGT[C/G]CAGTGGGCACTCTCT	22937
rs575787353	snp	A/T	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47445385	CTGAGTAGCTGGGAT[A/T]ACAAGTGCCCGCCAC	22937
rs575829749	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47426788	ATCAGAAGCACCTCG[A/G]GTGCCCTTGCCAATT	22937
rs575905837	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47442699	GCCAGGACTATTTTA[C/T]TATATTAGCTAACCA	22937
rs575916218	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47433476	CATCACACCCCTTAC[A/G]GCCTCATCATTAAAC	22937
rs575943750	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47427394	CACACATCAAAAAGA[C/T]GGTGACCAATGGGCA	22937
rs575950563	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47421612	ACCACAGTGCTACTC[C/T]GATCTGGGGTAAGAC	22937
rs575976058	snp	A/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47428359	CGTAGACCCACAAGG[A/T]TGCTGAGAAATTCAA	22937
rs575999247	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47451785	TCTACTAATGCTGTG[A/G]GCTGGATACCCTTCT	22937
rs576064429	snp	A/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47452440	TAGGACAGTGCTCAG[A/T]ACATATCTTCTCAAC	22937
rs576219343	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47434505	AACAGTACAGTCCAG[A/G]AGGAGGAGTGGGCTG	22937
rs576240581	snp	C/T	0.00358779	0.0422022	intron-variant	SCAP	GRCh38.p7	3:47469156	AGTTCAAGACCAGCC[C/T]GGCCAACATGGTGAA	22937
rs576267172	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47420240	TGAACCCGACCCAGG[A/G]CAATGTGGTGGCCAC	22937
rs576271267	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47477567	CAGAGCGAGACTCCG[C/T]CTCAAAAAAAAAAAG	22937
rs576294067	in-del	-/GCGGCG	0.00850876	0.0646682	cds-indel, intron-variant, upstream-variant-2KB	SCAP, LOC105377073	GRCh38.p7	3:47475824	AGCACCTCCCAAGCT[-/GCGGCG]GCGGCGGCGGCGGCG	22937
rs576433381	snp	C/G	2.10746e-05	0.00324605	missense	SCAP	GRCh38.p7	3:47418689	CATGGGCCTGCACCC[C/G]ACCTGGGCCCTTGGG	22937
rs576441693	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime, intron-variant, upstream-variant-2KB	SCAP, LOC105377073	GRCh38.p7	3:47475831	CCCAAGCTGCGGCGG[C/T]GGCGGCGGCGGCGAC	22937
rs576504539	snp	G/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47424705	TGGGGGAGGGTGGTG[G/T]TTAACAGTGTCAAGC	22937
rs576537947	snp	G/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47432134	CCATCCTGGCCAACA[G/T]GGTGAAACCCCGTCT	22937
rs576548407	snp	A/G	0.00199481	0.0315187	intron-variant	SCAP	GRCh38.p7	3:47468145	TTGGGTTGGTTCCAA[A/G]TCTTTGCTATTGTGA	22937
rs576583430	snp	A/G	0.00478085	0.0486577	upstream-variant-2KB, utr-variant-5-prime, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47476093	ATGGACGGCCGGGCC[A/G]GGCCGGGCCGGGCGG	22937
rs576593088	snp	A/T			intron-variant	SCAP	GRCh38.p7	3:47459726	CAAAGGCAAATTCAG[A/T]ACTACTGATAAGGGT	22937
rs576608784	snp	A/C/G	3.3127e-05	0.00406972	intron-variant	SCAP	GRCh38.p7	3:47421055	AGCACATGGGGATGG[A/C/G]GGGGTGCCGTGACCT	22937
rs576621647	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47425216	TACACAAACATACCA[A/G]CACACACCCCTTATA	22937
rs576666008	snp	A/C	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47459757	CTATGTTCAGCTGTG[A/C]ACGTATTGTCTTGAT	22937
rs576717860	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	PTPN23, SCAP	GRCh38.p7	3:47413537	GGATGGTACCAAACT[A/G]CCACACTACCAGGAC	22937
rs576765507	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47421531	AAAGGGTGAGCTCTC[C/T]GCTCCCCAAGCTCTG	22937
rs576765831	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47415046	GCAATGGGTAGACGG[C/T]CCCTGCCCGTCCCAC	22937
rs576790354	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47460298	TAAAGTAAGACAAGC[A/G]TAAGAAATTATAAAG	22937
rs576801768	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47476184	GAACTTGCAGAAAGC[C/T]GGGCACGGTGGCTCG	22937
rs576834373	snp	A/C	1.65151e-05	0.00287355	intron-variant, missense, utr-variant-5-prime	SCAP	GRCh38.p7	3:47427620	CTAAGGCCTGGCAGC[A/C]GGTCGGTCACTTGCA	22937
rs576872582	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47435266	TGTGCAAAATATTAG[A/G]ATCACAAAATTGCAA	22937
rs576897449	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47444402	AACTCAAAAGCCAAA[A/G]GGAATGCCTATTGCT	22937
rs576942700	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47428304	GAGACTCAAGGCTAT[A/G]TGTGTGCCATCTGCA	22937
rs576959248	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47440108	GCAGCTCAGGTGGCT[A/G]TTAGATCTGAATAGG	22937
rs576969400	snp	C/G	0.0023933	0.0345097	intron-variant	SCAP	GRCh38.p7	3:47416109	GGGACGCCCCCTCCC[C/G]AAGGAAAAAGACTCC	22937
rs577064924	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47438649	TGAAACCCCGTCTTT[A/C]CTAAAAAAACAAAAA	22937
rs577085771	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47470112	CTAAAATATTTACAT[A/G]CTGCAAATTATTTTC	22937
rs577124107	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47442501	TAATGGACTTTGCCT[C/T]GCAACACACAAAAAA	22937
rs577253582	snp	C/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47468223	GATTTATAATCCTTT[C/G]GGTATATGCCCAGTA	22937
rs577290636	snp	A/G			upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47477890	CAGGCATGAGCCACC[A/G]TGCCCATCCTGTTTG	22937
rs577291194	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47438542	ATTTAGGCTGGGCAC[A/G]GTGGCTCACGCCTGT	22937
rs577319711	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47460887	ACGTTGCATGGAAGA[A/G]GGTTCCAAACAGTGC	22937
rs577365320	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47420011	TCCACCTCAGCTGGA[A/G]CCAGAAAGCTGCTAC	22937
rs577627744	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47452569	ATCCTGTTCTTCACA[A/G]ATGTCCCAATCTAAA	22937
rs577652909	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47456723	TGAGCCGAGATCATC[C/T]GAGATCGTGTGAGAT	22937
rs577684342	snp	C/T	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47459479	TCCGTAAGTGTCGGC[C/T]GGCTGAGAAATAAAG	22937
rs577866140	snp	A/G	0.00119737	0.0244387	intron-variant	SCAP	GRCh38.p7	3:47432978	TCCCTTTTATCCTCC[A/G]CTGGATTGGATGATG	22937
rs577868870	snp	A/G	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47418072	GGGGAGATACGTGGC[A/G]GCGGGGGGTGGGGTG	22937
rs577957837	snp	C/T	0.0023933	0.0345097	intron-variant	SCAP	GRCh38.p7	3:47424608	TCTATGTGCGAGGAA[C/T]GCCAGCCAAGTTATA	22937
rs577957885	snp	A/G	0.000399281	0.0141238	missense	SCAP	GRCh38.p7	3:47417464	AGCACCGGCCCAGGC[A/G]AGGGTGGGCGCAGGG	22937
rs578035781	snp	C/T	0.000399281	0.0141238	intron-variant	SCAP	GRCh38.p7	3:47439472	ATCCACCTCTCACCA[C/T]GAGCAGCAGCTTGTT	22937
rs578107362	snp	C/T	0.000798403	0.0199641	intron-variant	SCAP	GRCh38.p7	3:47431765	ACCCCAATCACTTAC[C/T]GTAGGAGGTGTCTGT	22937
rs578145127	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47432538	CATCATCCCACACCA[C/T]GCGTATGCAATAAAC	22937
rs578213584	snp	C/T	0.00159617	0.0282053	intron-variant	SCAP	GRCh38.p7	3:47467325	AAGAAGATATACAGG[C/T]TCGGTGGGGTGGCTC	22937
rs745317582	in-del	-/AA			intron-variant	SCAP	GRCh38.p7	3:47432316	AAGACTCCGTCTTGA[-/AA]AAAAAAAAAAAAAAA	22937
rs745318827	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47440772	GGCTGAGGTAGGAGA[A/C]TCACTTGAGCCCATG	22937
rs745329825	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47424564	CTGAGCCCACTGTCC[C/T]ACACTCCCCGCAGCA	22937
rs745356806	snp	C/T	3.40084e-05	0.00412347	missense	SCAP	GRCh38.p7	3:47415134	GGGCAGTGTGGGTCT[C/T]CAAGGAGAAGAAATC	22937
rs745402503	snp	C/T	1.65408e-05	0.00287578	missense, intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47426087	CCTCCTTGAAGTGCA[C/T]GTGGACCAGGCTCTC	22937
rs745402843	snp	G/T	3.71374e-05	0.00430898	intron-variant	SCAP	GRCh38.p7	3:47419720	CTGCAGTGGGGCAGG[G/T]GGTACTCAGTGGGAG	22937
rs745442359	snp	A/G	0.000184894	0.00961316	synonymous-codon	SCAP	GRCh38.p7	3:47418363	CACGATCTCCGTCTC[A/G]GGTGGCGCATAGCCG	22937
rs745451260	in-del	-/CT			intron-variant	SCAP	GRCh38.p7	3:47427742	TACTTAGGGGACATC[-/CT]CTGTCTGTTCTTCAA	22937
rs745456038	snp	A/G	2.05696e-05	0.00320692	missense	SCAP	GRCh38.p7	3:47420583	GTGCCAGGCGGGTGC[A/G]GGCCAGGAAGTAGAC	22937
rs745567428	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47439240	ATGGTGAAACCCCGT[A/C]TCTACTAAAAATACA	22937
rs745624353	snp	G/T			intron-variant	SCAP	GRCh38.p7	3:47451593	TAATAGAGATGGGGT[G/T]TTACCATGTTGCCCA	22937
rs745676026	snp	C/T	2.16326e-05	0.00328874	synonymous-codon	SCAP	GRCh38.p7	3:47418720	TCCTGCTTCCCAGTG[C/T]CCAGCAGGTATGGGC	22937
rs745741259	in-del	-/AGGGCAGGGC			intron-variant	SCAP	GRCh38.p7	3:47420524	CCGGCCCTCCAGAAG[-/AGGGCAGGGC]AGGGCAGGGGTGGCA	22937
rs745778283	snp	C/T			intron-variant, upstream-variant-2KB	SCAP, LOC105377073	GRCh38.p7	3:47475644	GCCTCCTTGCCGGCC[C/T]GCGGTCTCCAGGGCC	22937
rs745791819	snp	A/G	3.2963e-05	0.00405961	utr-variant-5-prime, missense	SCAP	GRCh38.p7	3:47435066	TCCACAGGTGGGGGC[A/G]AGTAATCCTTCACAG	22937
rs745804123	snp	G/T			intron-variant	SCAP	GRCh38.p7	3:47462920	TTCCTCATCTACCCT[G/T]TCTCCCCAGGGCTTC	22937
rs745811492	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47440200	AAAGGTAAGCAATTA[A/G]ATGGAAACTGAATGT	22937
rs745856361	snp	A/G	1.69971e-05	0.00291518	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47425969	TTTAGCTTGGAGAAA[A/G]CCCTCAGCCTCCCTG	22937
rs745856377	in-del	-/CA	1.64953e-05	0.00287182	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47427408	ACGGTGACCAATGGG[-/CA]CCTTTACAGGTCTGA	22937
rs745882687	snp	C/T	1.82934e-05	0.0030243	missense	SCAP	GRCh38.p7	3:47417795	CCTGAGCCTCAAGCC[C/T]GCTGCCCACGCCACT	22937
rs745910644	snp	G/T	6.41993e-05	0.00566529	intron-variant	SCAP	GRCh38.p7	3:47417870	GGGCACGGGGGAGGG[G/T]GGTGAGAGGGGGCGG	22937
rs745969790	in-del	-/AAG			intron-variant	SCAP	GRCh38.p7	3:47459314	TGCCTGATTTCCTGC[-/AAG]AAGCGTGCTTTGCTG	22937
rs746034298	in-del	-/G			intron-variant	SCAP	GRCh38.p7	3:47452860	TGGGACACTGAGGCA[-/G]GAAGACTGCTTGAGG	22937
rs746102155	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47459825	GAGAACCGGTCTGAC[C/T]TCAAATTTACCAGGG	22937
rs746109680	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47459332	AAGCGTGCTTTGCTG[C/G]AGGGCATCAAAGCTC	22937
rs746131319	snp	A/C/T	3.29485e-05	0.00405874	intron-variant, missense, upstream-variant-2KB	SCAP	GRCh38.p7	3:47427191	AGACCAGGGTGATGG[A/C/T]GTAGGAGACCATCCT	22937
rs746142162	snp	C/T	5.00463e-05	0.00500206	missense	SCAP	GRCh38.p7	3:47420703	GCCGCTCGTAGCGCG[C/T]TGGCTGTCCCACTGG	22937
rs746164879	snp	A/C	0.00011961	0.00773245	intron-variant	SCAP	GRCh38.p7	3:47417231	CCAGAGGCTGTGAGC[A/C]CCTGCCAGCCAGAAA	22937
rs746170452	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47431878	TTAGGATACATTACT[C/T]AGAATTTTTTTGCCC	22937
rs746193507	snp	C/T	1.66032e-05	0.0028812	missense	SCAP	GRCh38.p7	3:47414645	CACGAGTCCTCCAGA[C/T]GGAACACCTGGGACA	22937
rs746199202	snp	A/G	0.000315259	0.0125511	synonymous-codon	SCAP	GRCh38.p7	3:47417493	GGCTGGTGTGCAGAC[A/G]GCCGCCAGCCCCTCC	22937
rs746228909	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47468472	TCTGATGGCCAGTGA[C/T]GACAAGCATTTTTTC	22937
rs746273150	snp	C/G	2.30886e-05	0.00339761	intron-variant	SCAP	GRCh38.p7	3:47427709	TGCTGTGTCTGCCAC[C/G]ACAGGGCAGACCTGC	22937
rs746283910	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47432877	CATTCCCAGCAAGGT[A/G]CTGACAACAACAATG	22937
rs746314740	snp	A/G	3.36383e-05	0.00410098	intron-variant	SCAP	GRCh38.p7	3:47423926	CCCAACTCTCCCACT[A/G]CGTTACCTTGGGCGA	22937
rs746325606	snp	C/T	1.68094e-05	0.00289904	missense	SCAP	GRCh38.p7	3:47417566	GGGGAGTCCCGAGAG[C/T]GGCCACAGACCGCCC	22937
rs746361918	snp	A/G	5.23766e-05	0.00511718	intron-variant	SCAP	GRCh38.p7	3:47414794	ACCCCGTGCCGGGCC[A/G]CTCCAGCACCCAAGA	22937
rs746382022	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47469303	GGTGAGCAGAGACCA[C/T]GCCGTTGCATTCCAG	22937
rs746439035	snp	A/C	1.79322e-05	0.00299429	intron-variant	SCAP	GRCh38.p7	3:47419296	GAGTTGACACCATCG[A/C]GTGAGGTGGCACCTG	22937
rs746476477	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47458016	AAAAAGGTCGGGCAC[A/G]GTGGCTCACGCCTGT	22937
rs746479615	snp	G/T			intron-variant	SCAP	GRCh38.p7	3:47464377	TGGGACTGATTTGTG[G/T]TTTTTTTTTTAAAGT	22937
rs746527463	in-del	-/T			intron-variant	SCAP	GRCh38.p7	3:47450512	TGATTATATGCAGGG[-/T]TTTTTTTTTTTTTTC	22937
rs746555026	snp	A/G	0.000154158	0.00877812	synonymous-codon	SCAP	GRCh38.p7	3:47418438	ACCACCCAGCTGCCC[A/G]TAGTTGCGCGGGCAT	22937
rs746578522	snp	A/G	0.000139811	0.00835979	missense	SCAP	GRCh38.p7	3:47418514	GTGGCCAGGCCCAGC[A/G]CCGCCACCCTGCACG	22937
rs746622696	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47439719	CCATAATGCCTATTT[A/G]CTACACATTTCATCA	22937
rs746637981	snp	A/G	1.6953e-05	0.0029114	intron-variant	SCAP	GRCh38.p7	3:47428475	TCCCTTCAGTACAGA[A/G]TGGGATTCAGGGAGG	22937
rs746639717	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47458863	CAGGCTGACGTGCAA[C/T]GGCGTGATCTCGGCT	22937
rs746644109	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47443126	GCCAGTTAACAAAGA[A/G]TACTTGGCTCTGCAC	22937
rs746678809	in-del	-/CTGT	4.95712e-05	0.00497827	frameshift-variant	SCAP	GRCh38.p7	3:47413988	TCTTCCCCAGGTAGA[-/CTGT]CTGTAACAGGTCCCC	22937
rs746787082	snp	A/C	1.65244e-05	0.00287436	intron-variant	SCAP	GRCh38.p7	3:47442834	CCTACTGTCCTAAGA[A/C]ACTGGCCCACCATAT	22937
rs746819236	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47421045	CTGGAATCAGAGCAC[A/G]TGGGGATGGGGGGGT	22937
rs746821251	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47437177	AGGCACAGTGGCTCA[C/T]GCCTGTAATCCCAGC	22937
rs746870930	snp	A/G	1.72124e-05	0.00293359	missense	SCAP	GRCh38.p7	3:47415164	CAAGGGAACCGTTGA[A/G]CCGTGCAGCCACAAT	22937
rs746891495	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47466399	TTCACACACATGTGA[A/G]ATGAGTCATTCTTGA	22937
rs746894108	snp	A/G	4.2115e-05	0.00458865	intron-variant	SCAP	GRCh38.p7	3:47417856	GGCGGAGTGAGAGGG[A/G]GCACGGGGGAGGGGG	22937
rs746936099	snp	C/G	1.65523e-05	0.00287678	missense, intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47426093	TGAAGTGCACGTGGA[C/G]CAGGCTCTCCGCCCG	22937
rs746957455	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47469958	TGTGAAGAGAGAAGC[A/G]GTTTTGAAAGAAATG	22937
rs746972557	snp	A/G	3.38484e-05	0.00411376	intron-variant	SCAP	GRCh38.p7	3:47417116	GCTGAGGCAGGCCAC[A/G]CTCACCTTTTGTCCA	22937
rs746992646	snp	C/T	1.69937e-05	0.00291488	missense	SCAP	GRCh38.p7	3:47420621	AGCCTCTTGGGGAGC[C/T]GCAGGTTTCGGAAGG	22937
rs746992795	snp	A/G	1.68992e-05	0.00290677	utr-variant-5-prime, missense, intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47426147	GCAGAAGCATCAGGC[A/G]GGCACGCAGGCTGCC	22937
rs747016875	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47448569	TTTTTTTTTTTCATT[C/T]TATTTCGATCTCTGT	22937
rs747222086	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47460847	AGGCGTGAGCCACTG[C/T]GCCCAGCAAGAACTC	22937
rs747223030	snp	A/G	1.64953e-05	0.00287182	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47427406	AGACGGTGACCAATG[A/G]GCACCTTTACAGGTC	22937
rs747259009	snp	A/C/G	3.33529e-05	0.00408357	missense	SCAP	GRCh38.p7	3:47414296	AGGTGACATCCCCAC[A/C/G]GTGAGCAAACACATG	22937
rs747342276	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47461943	GGAGGCTGAGACAGG[A/C]GAATCACTTAAACCC	22937
rs747355793	snp	C/T	1.74187e-05	0.00295111	intron-variant	SCAP	GRCh38.p7	3:47414820	CAAGAGACAAGACAA[C/T]ACTCACTCTCAGTGT	22937
rs747377304	snp	G/T	1.95934e-05	0.00312991	stop-gained	SCAP	GRCh38.p7	3:47417649	GTTGGTGTCAATTAA[G/T]CAGGTGAGGTCAGGC	22937
rs747432537	snp	A/C	1.89245e-05	0.00307602	intron-variant	SCAP	GRCh38.p7	3:47424093	GTTGTGGTGGTTCCC[A/C]ACAGACTGGGGCCCT	22937
rs747446698	snp	A/G	5.79246e-05	0.00538135	missense	SCAP	GRCh38.p7	3:47417455	GCCTGGGACAGCACC[A/G]GCCCAGGCGAGGGTG	22937
rs747498133	in-del	-/ACACAC			intron-variant	SCAP	GRCh38.p7	3:47443238	AATCCCAAAATACAC[-/ACACAC]ACACACACACACACA	22937
rs747512899	in-del	-/TTT			intron-variant	SCAP	GRCh38.p7	3:47451395	CAGTCCTGGAATGCC[-/TTT]TTTTTTTTTTTTTTT	22937
rs747526376	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47473556	CTCTCATCTGTTCAA[C/T]GGGGGTGATGACACA	22937
rs747621578	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47467822	TGTTGGTGTGCTGCA[C/T]CCGTTAACTCGTCAT	22937
rs747663130	snp	C/T	0.0001036	0.00719648	missense	SCAP	GRCh38.p7	3:47417581	CGGCCACAGACCGCC[C/T]GGTGCCGGGGCTCGG	22937
rs747668597	snp	C/T	1.64784e-05	0.00287035	intron-variant, missense, utr-variant-5-prime	SCAP	GRCh38.p7	3:47428583	AAGGTGAACGAAATA[C/T]ATCTACTGCCAGGAG	22937
rs747675096	snp	A/G			utr-variant-3-prime, downstream-variant-500B	PTPN23, SCAP	GRCh38.p7	3:47413348	GGGTGGAAATGTACT[A/G]CAGGCTCTGGGTCAG	22937
rs747700202	in-del	-/T	1.94642e-05	0.00311957	intron-variant, splice-acceptor-variant	SCAP	GRCh38.p7	3:47417828	CCCGGCGCTGCCTGC[-/T]GGGGGCCAGGAGGGC	22937
rs747708395	snp	A/G	1.90638e-05	0.00308732	missense	SCAP	GRCh38.p7	3:47417663	AGCAGGTGAGGTCAG[A/G]CTGGTCCCCGAAGAG	22937
rs747789018	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47469122	GGATGCCAAGGTGGG[A/C]AGATCACTTGAGGTC	22937
rs747792802	snp	C/T	1.79651e-05	0.00299704	intron-variant	SCAP	GRCh38.p7	3:47425448	CTCTCTGGCCTGAGC[C/T]CACCCTGTGGCCCAG	22937
rs747792846	snp	C/T	1.65974e-05	0.0028807	intron-variant, utr-variant-5-prime	SCAP	GRCh38.p7	3:47434943	AATCTCACTGGCAGA[C/T]CCCTGCCTCAGCCAG	22937
rs747815275	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47466532	TTGACAAAGATGCCA[C/T]GACCAGTCACTGGGG	22937
rs747842584	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47433548	GGAAACACAAATATT[C/T]CCTTATGTGCTAACA	22937
rs747845894	snp	A/G	1.65671e-05	0.00287807	synonymous-codon, intron-variant, utr-variant-5-prime	SCAP	GRCh38.p7	3:47425565	GAGCACTGTGACCAC[A/G]GCAGCCAGGGCCAGC	22937
rs747851823	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47422256	AGGGTTTGCTGAGCA[C/G]TTCTGAGCCAGGCAT	22937
rs747867283	snp	C/T			intron-variant, missense, utr-variant-5-prime	SCAP	GRCh38.p7	3:47428606	GCCAGGAGGTTCTTG[C/T]GCCAGGGAAACACTG	22937
rs747923303	snp	A/G	3.77415e-05	0.00434389	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47426186	TGGTCAAGGAGCAGG[A/G]TGGGGGTAAATGGAA	22937
rs747926131	snp	C/T			upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47477340	AACACGGGCAGATCA[C/T]GAGGTCAGGAGATCG	22937
rs747934587	snp	A/C/G	5.02938e-05	0.00501442	missense, synonymous-codon	SCAP	GRCh38.p7	3:47417133	TCACCTTTTGTCCAA[A/C/G]AACACCAGAGCGGTA	22937
rs747971670	in-del	-/CA			intron-variant	SCAP	GRCh38.p7	3:47463956	CCCATCTCAGCCTCT[-/CA]CACTGCTGGGACTAC	22937
rs747973512	in-del	-/T	1.66029e-05	0.00288117	intron-variant	SCAP	GRCh38.p7	3:47414163	CCAAGAATCCTATGA[-/T]TCCCCATCCCCTCTA	22937
rs747983991	snp	C/T	1.79181e-05	0.00299311	intron-variant	SCAP	GRCh38.p7	3:47423886	GAGGAACAGGCCCCA[C/T]TCCAGCCCCTCCTGC	22937
rs747999475	snp	A/G	6.63064e-05	0.0057575	synonymous-codon	SCAP	GRCh38.p7	3:47414061	AGTCACCAGCAGGTT[A/G]TCTGAGATGACACCC	22937
rs748019207	snp	A/G	1.66852e-05	0.0028883	missense	SCAP	GRCh38.p7	3:47420700	GCTGCCGCTCGTAGC[A/G]CGTTGGCTGTCCCAC	22937
rs748061181	snp	A/G	1.68593e-05	0.00290334	intron-variant	SCAP	GRCh38.p7	3:47417221	ACCTACGAGTCCAGA[A/G]GCTGTGAGCACCTGC	22937
rs748073348	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47453798	CCTACATTCCCACTT[C/T]CCACACCTTTGCAGT	22937
rs748104677	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47435471	TATAATATAAACATA[A/C]ACACACACACACACA	22937
rs748132117	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47433360	TGAGCGCTCCAATCA[C/G]AGAGAGAGGAAATGG	22937
rs748133425	snp	C/G	1.65971e-05	0.00288067	intron-variant	SCAP	GRCh38.p7	3:47414150	CCTTCCCTAAAATCC[C/G]AAGAATCCTATGATC	22937
rs748149812	snp	A/C	8.44587e-05	0.00649786	intron-variant	SCAP	GRCh38.p7	3:47420805	GTCAGGGCCTGAGTC[A/C]ACCATCCAGAGGCTG	22937
rs748205031	snp	A/G	1.68869e-05	0.00290571	missense	SCAP	GRCh38.p7	3:47417396	TGGGGGCCCAGGCGA[A/G]GGAAGGGGAGCCTTT	22937
rs748207050	snp	C/T	3.33979e-05	0.0040863	missense	SCAP	GRCh38.p7	3:47414319	AACACATGGCTGACC[C/T]GGCTGCCAGTCAGTA	22937
rs748233058	in-del	-/A	1.64789e-05	0.0028704	intron-variant, frameshift-variant, utr-variant-5-prime	SCAP	GRCh38.p7	3:47428560	ACCAGTTGGAATGCC[-/A]CGGGACAAAGGTGAA	22937
rs748234682	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47424456	CACAGCTAAATGCAA[A/G]GAGATGAAACCATCC	22937
rs748249100	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47419098	CCACTCCTGGCACAG[A/G]TGGGTGGGTCTCATT	22937
rs748324729	snp	C/T	2.23391e-05	0.00334202	synonymous-codon	SCAP	GRCh38.p7	3:47418735	CCCAGCAGGTATGGG[C/T]CCCGGTGGGGGCCAG	22937
rs748331800	snp	C/T	1.66084e-05	0.00288165	intron-variant	SCAP	GRCh38.p7	3:47414530	GTCAGCAAACATGGG[C/T]CACAGACTCTGTACC	22937
rs748345753	snp	C/T	1.65195e-05	0.00287393	missense	SCAP	GRCh38.p7	3:47422480	AGTAGCCGATGAGGA[C/T]GATGCCCAGCTCCGT	22937
rs748376286	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47448673	GAGCCCACCCAATTA[A/C]TTTTTCATTTAGGTT	22937
rs748411472	in-del	-/AAT			intron-variant	SCAP	GRCh38.p7	3:47472461	AAAAAAATAAAATAA[-/AAT]AATAATAATAATAAT	22937
rs748427248	in-del	-/AG	1.67674e-05	0.00289541	frameshift-variant	SCAP	GRCh38.p7	3:47420743	GGGCAGGCAGGCCTC[-/AG]GGGGCAGTCGCTTGT	22937
rs748446002	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47432402	GGGGAGCTCTTTCGA[C/T]TGCCCCCCTATGTCT	22937
rs748447667	snp	C/T	9.25412e-05	0.00680162	missense	SCAP	GRCh38.p7	3:47418805	TCCCTCGGGTTCAGG[C/T]GGAGCGTGACTGGGA	22937
rs748528276	snp	A/C			intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47427410	GGTGACCAATGGGCA[A/C]CTTTACAGGTCTGAA	22937
rs748532080	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47444432	TCGTTCTACCTTTCC[A/G]AAAGCAGAAGCGTTA	22937
rs748535042	snp	C/T	1.83004e-05	0.00302488	missense	SCAP	GRCh38.p7	3:47419683	TGTATACCAGGATGC[C/T]AATCCAGACAACGGT	22937
rs748535943	snp	C/T	0.000389781	0.0139549	intron-variant	SCAP	GRCh38.p7	3:47415024	CAAGTGAAGAATCTC[C/T]GAGAAAGCAATGGGT	22937
rs748555146	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47459916	CCTTATCTCAACCGC[A/G]TAAGACAGACACTCC	22937
rs748563949	snp	C/G	1.71917e-05	0.00293182	intron-variant, utr-variant-3-prime, downstream-variant-500B	PTPN23, SCAP	GRCh38.p7	3:47413814	GCATTGGCCCCCACA[C/G]AGCACCCCAGCCTCC	22937
rs748571629	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47458117	ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA	22937
rs748595770	in-del	-/ATC			intron-variant	SCAP	GRCh38.p7	3:47442579	AAAGAAAACTGAAGT[-/ATC]ATATCTTTCAATTAT	22937
rs748621732	snp	A/G	0.000188555	0.00970782	intron-variant	SCAP	GRCh38.p7	3:47418262	GTCCTGCAGAAGCCC[A/G]GTGTTGGTATGGGCC	22937
rs748658270	snp	C/T			intron-variant, upstream-variant-2KB	SCAP, LOC105377073	GRCh38.p7	3:47474765	TCGCGCCACTGCACT[C/T]CAGCCTGGGAGACAG	22937
rs748659730	snp	A/C	9.80056e-05	0.00699951	synonymous-codon	SCAP	GRCh38.p7	3:47418348	GCGCAGCACAAGCGG[A/C]ACGATCTCCGTCTCG	22937
rs748695163	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47461598	AAACTGAGGCTTAGG[A/G]AAGGTCATGCCAGAT	22937
rs748720251	snp	A/G	7.63271e-05	0.0061772	synonymous-codon	SCAP	GRCh38.p7	3:47417316	CACCTCCAGCCGGCC[A/G]CTGCTCCGCCCCACC	22937
rs748770376	snp	A/T			intron-variant	SCAP	GRCh38.p7	3:47456816	TAAGATCTGGAAAAA[A/T]ACAACTGCAATTCAT	22937
rs748776191	snp	A/G	1.648e-05	0.0028705	utr-variant-5-prime, missense	SCAP	GRCh38.p7	3:47435061	CAGAGTCCACAGGTG[A/G]GGGCGAGTAATCCTT	22937
rs748830994	snp	A/G	1.72107e-05	0.00293343	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47425953	GACATGGAAATGCCC[A/G]TTTAGCTTGGAGAAA	22937
rs748835570	snp	A/G	4.9894e-05	0.00499445	synonymous-codon, intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47425604	GGACTTGACCATGTC[A/G]ATCTTCCCTGGAGGG	22937
rs748902289	snp	C/T	1.77931e-05	0.00298266	intron-variant	SCAP	GRCh38.p7	3:47415043	AAAGCAATGGGTAGA[C/T]GGCCCCTGCCCGTCC	22937
rs748949326	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47465823	TGGGATTTCTTTCCA[C/T]TTACTTGTTTAAAAA	22937
rs748985541	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47470043	GGTAACTCTTTTAGA[C/T]TAATGTAATGGTAGC	22937
rs749003277	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47453978	GAAACATGTAAGTAC[C/T]AATGTTAAAACAATG	22937
rs749056011	snp	A/G	1.69714e-05	0.00291298	intron-variant	SCAP	GRCh38.p7	3:47420824	ATCCAGAGGCTGCTC[A/G]CACAGGACCGCTGTC	22937
rs749060905	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47425419	GGGAAGGCCAAGAAC[C/T]CAGAAGTGCAAGGCT	22937
rs749073716	in-del	-/A	8.52551e-05	0.00652842	intron-variant	SCAP	GRCh38.p7	3:47418892	CCTCCCAGGGCTTCC[-/A]TCCTGCTGTGCTCGC	22937
rs749110335	snp	A/C	0.000916741	0.02139	intron-variant	SCAP	GRCh38.p7	3:47418635	ACTCTTTCCCACCCC[A/C]CCCCACCCAGCAGCC	22937
rs749190706	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47447452	CCTAGAACTTGGTGA[A/G]GCAAAGGTGGGCGGA	22937
rs749194176	snp	A/G	6.66445e-05	0.00577216	synonymous-codon	SCAP	GRCh38.p7	3:47414282	GGTACAGGTAAGGGA[A/G]GTGACATCCCCACGG	22937
rs749204614	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47444510	ATAGAATCTCACTCT[A/G]TCGACCAGGCTGGAG	22937
rs749220404	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47439132	TGCATGACTAGGCTG[A/G]GCAAGGTGGCTTATG	22937
rs749236523	snp	A/G			upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47479056	GGTATGACCCACCAT[A/G]CCCAGCCTCCTACAA	22937
rs749267331	in-del	-/GTGAGAGGGGGCACGGGGGAGGGGG/GTGAGAGGGGGCATGGGGGAGGGGG	2.25629e-05	0.00335871	intron-variant	SCAP	GRCh38.p7	3:47417846	GGCCAGGAGGGCGGA[lengthTooLong]GTGAGAGGGGGCACG	22937
rs749278584	snp	A/T			intron-variant	SCAP	GRCh38.p7	3:47420544	AGGGCAGGGCAGGGG[A/T]GGCAGGTACCATGAT	22937
rs749293673	snp	A/C/T	0.000207035	0.0101724	missense	SCAP	GRCh38.p7	3:47417672	GGTCAGGCTGGTCCC[A/C/T]GAAGAGGGAAGGCGG	22937
rs749294616	snp	A/G	1.65373e-05	0.00287548	intron-variant, utr-variant-5-prime	SCAP	GRCh38.p7	3:47434958	CCCCTGCCTCAGCCA[A/G]TCTCCACCCAACGCT	22937
rs749300995	snp	C/G	2.10551e-05	0.00324455	missense	SCAP	GRCh38.p7	3:47418703	CCACCTGGGCCCTTG[C/G]GTCCTGCTTCCCAGT	22937
rs749317735	snp	C/T	1.66021e-05	0.0028811	missense	SCAP	GRCh38.p7	3:47414637	AGAGGCAGCACGAGT[C/T]CTCCAGACGGAACAC	22937
rs749349363	snp	A/G	2.32388e-05	0.00340864	missense	SCAP	GRCh38.p7	3:47418811	GGGTTCAGGCGGAGC[A/G]TGACTGGGATGACGG	22937
rs749376692	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47459476	TTTTCCGTAAGTGTC[A/G]GCCGGCTGAGAAATA	22937
rs749404146	snp	C/G	1.71628e-05	0.00292935	intron-variant	SCAP	GRCh38.p7	3:47423913	CTGCAGCCCTCTGCC[C/G]AACTCTCCCACTGCG	22937
rs749459359	snp	A/G	3.59874e-05	0.00424175	intron-variant	SCAP	GRCh38.p7	3:47419281	GGGAAAGGGGATGGT[A/G]AGTTGACACCATCGA	22937
rs749464407	snp	A/G	0.000152401	0.00872797	missense	SCAP	GRCh38.p7	3:47417819	CGCCACTGTCCCGGC[A/G]CTGCCTGCTGGGGGC	22937
rs749474668	in-del	-/C	8.30227e-05	0.0064424	intron-variant, utr-variant-5-prime	SCAP	GRCh38.p7	3:47434943	AATCTCACTGGCAGA[-/C]CCCTGCCTCAGCCAG	22937
rs749517170	snp	C/T	4.97525e-05	0.00498736	utr-variant-5-prime	SCAP	GRCh38.p7	3:47443001	AGGGTCATCCTCAGC[C/T]GAAGTCACCTTGCTG	22937
rs749524696	snp	G/T	1.64963e-05	0.00287192	utr-variant-5-prime, missense	SCAP	GRCh38.p7	3:47442878	AAAACATACCAGCAG[G/T]CTAAGATGCAGAACC	22937
rs749550679	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47435251	TCAGGACTGTACAAA[C/T]GTGCAAAATATTAGA	22937
rs749554318	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47423216	AAGTGACCAGGCCTC[C/T]AAGGCCAGGCTCTCC	22937
rs749578606	snp	C/T	0.00201569	0.0316825	intron-variant	SCAP	GRCh38.p7	3:47417860	GAGTGAGAGGGGGCA[C/T]GGGGGAGGGGGGTGA	22937
rs749661015	snp	A/T	3.29554e-05	0.00405914	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47427444	AACTTGTACTGGGGC[A/T]ACCTTTGAGTGTGGC	22937
rs749663154	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47430283	CTCACTAAATATCAC[A/G]TACTTTTCTCACTAG	22937
rs749684765	in-del	-/AC			intron-variant	SCAP	GRCh38.p7	3:47435465	ACATATATAATATAA[-/AC]ACATACACACACACA	22937
rs749756737	snp	C/T	0.000151217	0.00869401	missense	SCAP	GRCh38.p7	3:47417414	AAGGGGAGCCTTTCT[C/T]GGGGGAGCCACCCTC	22937
rs749766376	snp	C/T	3.96291e-05	0.00445118	missense	SCAP	GRCh38.p7	3:47417473	CCAGGCGAGGGTGGG[C/T]GCAGGGCTGGTGTGC	22937
rs749769930	snp	C/T	0.000143554	0.00847093	missense	SCAP	GRCh38.p7	3:47418409	AGCTCCCCGCGCCTC[C/T]GCCGCCCGGGCCCAC	22937
rs749774826	snp	A/T			intron-variant	SCAP	GRCh38.p7	3:47459734	AATTCAGAACTACTG[A/T]TAAGGGTCTATGTTC	22937
rs749779557	snp	A/C	1.64732e-05	0.0028699	intron-variant, synonymous-codon, upstream-variant-2KB, utr-variant-5-prime	SCAP	GRCh38.p7	3:47427553	ATTCTGCCAGAAGTT[A/C]CCAGGGGACAGCAGC	22937
rs749798854	snp	C/T	1.66021e-05	0.0028811	synonymous-codon, utr-variant-5-prime	SCAP	GRCh38.p7	3:47422523	CATGATGGACCAGCT[C/T]TCGCTGCTTAGGCCT	22937
rs749838742	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47458602	CCCAAATTGAAGTAA[A/G]ACCAAATTATATTAG	22937
rs749871464	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47420123	CTCCCATCTCAGTTC[A/G]GCTCCCTGGAAGAGG	22937
rs749877627	snp	A/G	3.02183e-05	0.00388693	intron-variant	SCAP	GRCh38.p7	3:47417852	GGAGGGCGGAGTGAG[A/G]GGGGGCACGGGGGAG	22937
rs749923410	snp	G/T	1.70107e-05	0.00291634	stop-gained	SCAP	GRCh38.p7	3:47419348	GGCCAGTGTGATGTT[G/T]TAATAGCTGAAGAGC	22937
rs749924550	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47442466	GGTTAGCCTGCCACA[A/G]GTTGTCCAAGATACT	22937
rs749967242	snp	A/G	8.25689e-05	0.00642477	utr-variant-5-prime, missense	SCAP	GRCh38.p7	3:47442957	GGTTGTAGAAGGCCC[A/G]AGATATCTTCTCACG	22937
rs750034280	snp	A/G	1.6821e-05	0.00290004	utr-variant-5-prime, synonymous-codon, intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47426144	GGTGCAGAAGCATCA[A/G]GCGGGCACGCAGGCT	22937
rs750036827	snp	A/G	3.40518e-05	0.00412611	intron-variant	SCAP	GRCh38.p7	3:47417110	TCTGGGGCTGAGGCA[A/G]GCCACGCTCACCTTT	22937
rs750044355	snp	A/G	0.000143606	0.00847245	intron-variant	SCAP	GRCh38.p7	3:47418108	GGTTGTGGGGGCACA[A/G]AGGAGGAAAGGGCAG	22937
rs750103551	snp	C/T	1.67128e-05	0.00289069	missense	SCAP	GRCh38.p7	3:47417186	TGCTGCAGCACAGCA[C/T]CCCTTCAATGGCGTC	22937
rs750103879	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47434507	CAGTACAGTCCAGAA[A/G]GAGGAGTGGGCTGGG	22937
rs750110358	snp	C/G	3.2993e-05	0.00406145	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47427148	AGCCCAGGGTACTGT[C/G]AATCTTACTTGGCAT	22937
rs750160844	snp	C/G	1.66882e-05	0.00288857	missense	SCAP	GRCh38.p7	3:47420686	CGGCCTCACAGCCAG[C/G]TGCCGCTCGTAGCGC	22937
rs750193430	snp	G/T			intron-variant	SCAP	GRCh38.p7	3:47465904	CTTTGGGAGGCCAAG[G/T]CAGGTGGGTCATGAG	22937
rs750204880	snp	C/T	0.000145762	0.00853579	synonymous-codon	SCAP	GRCh38.p7	3:47417454	GGCCTGGGACAGCAC[C/T]GGCCCAGGCGAGGGT	22937
rs750221799	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47428206	GACACCACCATTACA[C/T]TCACACCATAACCCA	22937
rs750257136	snp	A/C	3.37365e-05	0.00410696	intron-variant, stop-gained, utr-variant-5-prime	SCAP	GRCh38.p7	3:47427645	CTTGCAGACACAACT[A/C]CTCCAAGCTCCTGAT	22937
rs750277096	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47463087	CAAATCTAACAAGAC[C/T]AAAAACAGAATTCTT	22937
rs750444621	snp	C/T	4.17397e-05	0.00456816	intron-variant	SCAP	GRCh38.p7	3:47418871	AGTGGGCAGCCTCAG[C/T]GGGGGGCCTCCCAGG	22937
rs750453577	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47415963	AAAGGAGAATTTCCA[A/G]GAAGCATGGAGGGGC	22937
rs750478719	snp	C/G			upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47478306	CACCTAGCTAAGTAC[C/G]TTTGTGCCTTGAAGC	22937
rs750486395	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47440294	TGGAAGAAGGGGGCA[C/T]TGCTCTGCTGCTCTG	22937
rs750502951	snp	G/T	3.36253e-05	0.00410019	missense	SCAP	GRCh38.p7	3:47414917	TGCACAGGGCACTGT[G/T]TGGGTCAGGTGACAG	22937
rs750516026	snp	A/G	3.72946e-05	0.00431809	missense	SCAP	GRCh38.p7	3:47417689	AAGAGGGAAGGCGGC[A/G]GAGGGCCCCGGGGGC	22937
rs750537215	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47424905	GCCTGAGGACAAGCC[A/G]AGGGAAGGGCTTCCA	22937
rs750606288	in-del	-/G			intron-variant	SCAP	GRCh38.p7	3:47421643	CATGGAGTGCAGATA[-/G]TGGCACAGTGGTTGT	22937
rs750672909	snp	C/T	7.47524e-05	0.00611315	missense	SCAP	GRCh38.p7	3:47418225	TCACCAGCAGCATGC[C/T]GTCGCTGGCCAGGCA	22937
rs750706531	snp	A/G	1.79011e-05	0.00299169	synonymous-codon	SCAP	GRCh38.p7	3:47419636	TTCCGTCACCTGGGC[A/G]GCGAGGTAGTTGCGC	22937
rs750731829	snp	A/G	0.0001641	0.00905667	missense	SCAP	GRCh38.p7	3:47417578	GAGCGGCCACAGACC[A/G]CCCGGTGCCGGGGCT	22937
rs750736040	snp	A/G	1.67761e-05	0.00289617	synonymous-codon	SCAP	GRCh38.p7	3:47420743	GGGCAGGCAGGCCTC[A/G]GGGGGCAGTCGCTTG	22937
rs750780254	snp	C/T	1.65908e-05	0.00288012	intron-variant	SCAP	GRCh38.p7	3:47414128	CATGACAAGCTCAGT[C/T]CTGAGTCCTTCCCTA	22937
rs750805184	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47433009	CAAAAACATGGGGCT[C/G]AAGCTGCTAGGGCCA	22937
rs750837437	snp	G/T	4.98616e-05	0.00499283	missense	SCAP	GRCh38.p7	3:47414227	TGCGGTCCCAGATGC[G/T]GATGAGGTCATCCAG	22937
rs750839588	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47473849	TAATAAACTTGTAGT[A/G]AACTTTTTACCCACC	22937
rs750898360	in-del	-/TGCCCACC	0.000187776	0.00968776	utr-variant-3-prime, downstream-variant-500B	PTPN23, SCAP	GRCh38.p7	3:47413232	ATCATCATCATCTCA[-/TGCCCACC]TGCCCACACCCAGCA	22937
rs750968983	snp	C/T	0.000187521	0.00968117	synonymous-codon	SCAP	GRCh38.p7	3:47417625	TGAGGACCGAGGCTG[C/T]GCTGAAAAGTTGGTG	22937
rs750974062	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47443931	ACAGGAACTTGGATA[C/T]TCATGATGTTTATTC	22937
rs750980451	snp	A/G	1.66746e-05	0.00288739	intron-variant	SCAP	GRCh38.p7	3:47428684	TACTGCAGAAGAAAT[A/G]AGGGAGGGCAGAAAG	22937
rs750997532	in-del	-/C	1.73996e-05	0.00294949	intron-variant	SCAP	GRCh38.p7	3:47417257	AGAAAGGCCCACAAT[-/C]CCCGGGGCGGACAGC	22937
rs751008763	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47422161	CCACTTGGCTGAAAG[A/G]GAAGCAGGCAGGGAG	22937
rs751010401	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47460194	TATTGTTCAAACACA[C/T]GTTTTACAATCAATT	22937
rs751037268	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47428336	AGGTCCAAGCGGAAT[A/G]CAGCCACCGTAGACC	22937
rs751037461	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47463532	CATAGTGAAACCTTG[C/T]GTCTACTAAAAATAC	22937
rs751065512	in-del	-/AGCCCCTCTGCCCACCTCC	7.24323e-05	0.00601755	intron-variant	SCAP	GRCh38.p7	3:47417288	GCTCTGCCCACCTTT[-/AGCCCCTCTGCCCACCTCC]AGCCCCTCTGCCCAC	22937
rs751071982	snp	A/T	1.65979e-05	0.00288074	intron-variant	SCAP	GRCh38.p7	3:47414142	TCCTGAGTCCTTCCC[A/T]AAAATCCCAAGAATC	22937
rs751093608	snp	A/G	3.29685e-05	0.00405995	intron-variant, missense, upstream-variant-2KB	SCAP	GRCh38.p7	3:47427160	TGTCAATCTTACTTG[A/G]CATGGTAGTGCTGGA	22937
rs751097462	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47446432	CTCCTTCGCCTCCCA[A/C]AGGGCTGGGATTACA	22937
rs751109042	snp	G/T	5.08634e-05	0.00504273	synonymous-codon	SCAP	GRCh38.p7	3:47418187	CGCGTCCCACACGCA[G/T]ACGTGGCCTGCCAGG	22937
rs751142537	snp	A/G	1.64906e-05	0.00287142	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47427269	ATAACAAGTCTGCAA[A/G]CAGAAACCAGCAGGT	22937
rs751146724	snp	C/G	1.68485e-05	0.00290241	intron-variant	SCAP	GRCh38.p7	3:47420780	TCTGCTAGCTGTTGG[C/G]GGCACAGTGGTCAGG	22937
rs751147375	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47421124	GCCACCTCATAACCG[A/G]CAGGGCAGCAGCAGG	22937
rs751269061	snp	A/G	1.65034e-05	0.00287253	synonymous-codon	SCAP	GRCh38.p7	3:47420940	TCCTACCTCCATCCG[A/G]CGAATGTCAATGGAC	22937
rs751300538	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47453655	ACTAATAACTACTTT[C/T]ACTATTTCAGTTCCA	22937
rs751311642	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47421700	CCCTATCCTGCAGAT[A/G]CTACTGTTTTTCCAG	22937
rs751335638	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47415280	CAGTTCAAGAAGGCA[A/C]AGGAGGGACATGGCC	22937
rs751343503	snp	A/G	4.95552e-05	0.00497747	missense, intron-variant	SCAP	GRCh38.p7	3:47423968	ACCTCCAGGTCTACC[A/G]GGGTTGAGACCACAG	22937
rs751355170	snp	A/G	1.66275e-05	0.00288331	intron-variant	SCAP	GRCh38.p7	3:47414697	TCTCTGGGATTTTCC[A/G]AGTTATACTTTGGCT	22937
rs751542577	in-del	-/ACATACAC			intron-variant	SCAP	GRCh38.p7	3:47435466	ACATATATAATATAA[-/ACATACAC]ACACACACACACACA	22937
rs751570667	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47467597	AGAGCAAGAAGACCC[C/T]GTCTCAAGAAAAAGA	22937
rs751575082	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47431902	TTTGCCCAGGAGATT[C/T]GTCTATTGTCATCCA	22937
rs751586997	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47463917	ATCGTGGCTCACTGC[A/G]GTCTCAACCTCCCAA	22937
rs751598399	in-del	-/C			intron-variant	SCAP	GRCh38.p7	3:47424525	AGAAGAACGACTGTT[-/C]CTACACAAAGCTCTA	22937
rs751632124	snp	C/T			intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47426302	ACTTCTCTATGGTGC[C/T]TGAGCTTCTCTATAG	22937
rs751636317	snp	A/G	1.80136e-05	0.00300108	synonymous-codon	SCAP	GRCh38.p7	3:47419642	CACCTGGGCAGCGAG[A/G]TAGTTGCGCAGCCCT	22937
rs751679047	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47450971	CCCAGCTCAGCTTCC[C/T]GTGTAGCTAGGATTA	22937
rs751685965	snp	C/T	1.74549e-05	0.00295417	intron-variant	SCAP	GRCh38.p7	3:47415083	TGAACACCTGCCCAC[C/T]CCAGGCCCTCCGACC	22937
rs751688231	snp	A/G	3.56281e-05	0.00422052	intron-variant, utr-variant-3-prime, downstream-variant-500B	PTPN23, SCAP	GRCh38.p7	3:47413804	CAGGTTCAGTGCATT[A/G]GCCCCCACACAGCAC	22937
rs751693690	snp	C/T	3.32729e-05	0.00407864	intron-variant	SCAP	GRCh38.p7	3:47420510	AGGGGCCTGGAGCAC[C/T]GGCCCTCCAGAAGAG	22937
rs751741789	snp	A/C	0.000101559	0.00712525	synonymous-codon	SCAP	GRCh38.p7	3:47418339	GAGGTGGCCGCGCAG[A/C]ACAAGCGGCACGATC	22937
rs751790048	snp	A/T			intron-variant	SCAP	GRCh38.p7	3:47425150	TGTATATAGAATACA[A/T]AAACACAGACACACA	22937
rs751838887	snp	A/C	4.22003e-05	0.0045933	missense	SCAP	GRCh38.p7	3:47418688	CCATGGGCCTGCACC[A/C]CACCTGGGCCCTTGG	22937
rs751852601	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47442162	GAAGAACAGAATTCT[C/T]TCCAGAGAAAAGAAT	22937
rs751871591	snp	A/G	1.64727e-05	0.00286986	intron-variant, synonymous-codon, upstream-variant-2KB, utr-variant-5-prime	SCAP	GRCh38.p7	3:47427511	GGTCCCAATGATGTC[A/G]GGATCAGCATGGAAG	22937
rs751878751	snp	A/G			intron-variant, upstream-variant-2KB	SCAP, LOC105377073	GRCh38.p7	3:47474654	ATACAAAAATTAGCC[A/G]GGCGTGGTGGCACAC	22937
rs751943955	in-del	-/CTCCCCTCCTCCCT	0.000159324	0.00892395	intron-variant	SCAP	GRCh38.p7	3:47418570	CTCACAGCCTGTCCC[-/CTCCCCTCCTCCCT]CTCCCCTCCTCCCTC	22937
rs751957768	snp	A/G	1.65671e-05	0.00287807	synonymous-codon, intron-variant, utr-variant-5-prime	SCAP	GRCh38.p7	3:47425550	CATGAGCAGCGAGCT[A/G]AGCACTGTGACCACG	22937
rs752004657	snp	A/C	1.67363e-05	0.00289272	intron-variant	SCAP	GRCh38.p7	3:47434906	AGTACATGAATTCAC[A/C]AATCAGAAGCTGACC	22937
rs752006380	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47420226	CATGCAGCGGCCGAT[A/G]AACCCGACCCAGGGC	22937
rs752033323	snp	C/T			downstream-variant-500B, synonymous-codon	PTPN23, SCAP	GRCh38.p7	3:47413899	ATACACCAGGCTGAG[C/T]TCACTGCCAAAGTTG	22937
rs752063295	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47467702	AACATCAATATTCCT[C/T]AGAAAATACAAATTG	22937
rs752122003	snp	A/G	1.80798e-05	0.00300658	synonymous-codon	SCAP	GRCh38.p7	3:47417757	ACCAGCCTTCCCACC[A/G]TCTGAAAGTCGTTCC	22937
rs752127151	snp	A/C	5.2989e-05	0.00514701	intron-variant	SCAP	GRCh38.p7	3:47415002	GGGGTCCCTGAGGAC[A/C]AAAGGCCAAGTGAAG	22937
rs752150215	snp	C/T			synonymous-codon	SCAP	GRCh38.p7	3:47414330	GACCCGGCTGCCAGT[C/T]AGTACATCCCACAGG	22937
rs752150926	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47430092	TGCACACACCACACA[C/T]GCATACAAACAGTGT	22937
rs752179416	snp	C/G	1.70339e-05	0.00291833	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47425647	ATCAGGGCGGCCCCT[C/G]CCCCAGCCCCCGGCC	22937
rs752185806	in-del	-/AGG	3.43885e-05	0.00414645	intron-variant	SCAP	GRCh38.p7	3:47424059	CGCTGGGGACAGAGA[-/AGG]AGAAGGTGAGGACAG	22937
rs752237681	snp	C/T	8.59784e-05	0.00655605	missense	SCAP	GRCh38.p7	3:47417375	TCCAGATGGAACCCT[C/T]GGCACTGGGGGCCCA	22937
rs752238656	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47414422	AGTGGGGTCACCATG[C/G]TGTAATACCTCTGTC	22937
rs752304672	snp	A/G	2.10374e-05	0.00324318	missense	SCAP	GRCh38.p7	3:47418694	GCCTGCACCCCACCT[A/G]GGCCCTTGGGTCCTG	22937
rs752375483	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47460324	TAAAGTATTAATTTT[A/G]GGAACTGATAAATGT	22937
rs752381884	in-del	-/CGGTGGGGG	0.000112169	0.00748813	cds-indel	SCAP	GRCh38.p7	3:47418738	AGCAGGTATGGGCCC[-/CGGTGGGGG]CCAGGCACTGCGGCC	22937
rs752400239	snp	A/G	3.70762e-05	0.00430543	missense	SCAP	GRCh38.p7	3:47417702	GCGGAGGGCCCCGGG[A/G]GCGGTGTCTCAGGGG	22937
rs752462659	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47440479	AAAATTTTCTCAAGT[C/G]AATCAGGTTTTAAGA	22937
rs752480524	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47457639	TGGGCCGGGCACGGT[A/G]GCTCACGTCTATAAT	22937
rs752487428	in-del	-/CC			intron-variant, utr-variant-3-prime, downstream-variant-500B	PTPN23, SCAP	GRCh38.p7	3:47413779	GATACTCGGCTCTTT[-/CC]CCCAAGTCCAGGTTC	22937
rs752507188	snp	G/T	1.71781e-05	0.00293066	missense	SCAP	GRCh38.p7	3:47418144	CCTACCCTGGGCGCG[G/T]AATGCGCGTTAGGCA	22937
rs752537249	snp	G/T	1.83122e-05	0.00302585	utr-variant-3-prime, downstream-variant-500B	PTPN23, SCAP	GRCh38.p7	3:47413208	TTGCCTACCTGGTCC[G/T]TACACTACATCATCA	22937
rs752567413	in-del	-/TTTTTTTTT			intron-variant	SCAP	GRCh38.p7	3:47416617	CACACCCCTAACGCT[-/TTTTTTTTT]TTTTTTTTTTTTTTT	22937
rs752620582	snp	A/G	1.64792e-05	0.00287042	intron-variant, synonymous-codon, upstream-variant-2KB	SCAP	GRCh38.p7	3:47427168	TTACTTGGCATGGTA[A/G]TGCTGGAAGACCAGG	22937
rs752628739	snp	A/G	6.46684e-05	0.00568595	synonymous-codon	SCAP	GRCh38.p7	3:47418205	GTGGCCTGCCAGGCA[A/G]CAGCTCACCAGCAGC	22937
rs752635396	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47455360	AGCAACTTGGGAGGC[C/T]GAGATGGGCAGATCA	22937
rs752640545	snp	A/G	1.65179e-05	0.00287379	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47427299	TACTGACACAGAAAT[A/G]ACAGCTACTGCAGAG	22937
rs752658647	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47469873	AAGAGAGCTCTCAGA[C/T]TGGAACAAGAAATTA	22937
rs752683819	snp	A/G	0.00013371	0.0081754	missense	SCAP	GRCh38.p7	3:47420661	GCAACGTGATGGTGT[A/G]GGGTGTGGACGGCCT	22937
rs752711128	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47467023	GCTTGAGTCCAGGAA[A/G]TGGAGGCTGCAATGA	22937
rs752714053	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47464267	GTGATCCGCCTGCCT[A/C]GGCCTCTCAAAGTGC	22937
rs752720257	in-del	-/CC			intron-variant	SCAP	GRCh38.p7	3:47443306	TCTCTCTCTCTCTCT[-/CC]CTCTCCCTCCCCGCC	22937
rs752744947	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47453266	ACCTGCTTATGGCCA[A/G]GCACAGTGGCTCACA	22937
rs752746707	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47470794	TGAACCCAGGGGGGC[A/G]AAGGTTGCAGTGAGC	22937
rs752759779	snp	A/T			intron-variant	SCAP	GRCh38.p7	3:47452446	AGTGCTCAGTACATA[A/T]CTTCTCAACTTCTAA	22937
rs752808226	snp	A/G	1.81757e-05	0.00301455	intron-variant, synonymous-codon, utr-variant-5-prime	SCAP	GRCh38.p7	3:47427667	GCTCCTGATCCCAGA[A/G]CTGCACAGGAGACAG	22937
rs752824363	in-del	-/CAGTACTT			intron-variant	SCAP	GRCh38.p7	3:47444774	ACCACCACACCCGGC[-/CAGTACTT]CATTACTTTTTTTTT	22937
rs752831413	snp	G/T			intron-variant, utr-variant-5-prime	SCAP	GRCh38.p7	3:47434954	CAGACCCCTGCCTCA[G/T]CCAGTCTCCACCCAA	22937
rs752891216	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47463997	CCACCACATCTGGCT[A/G]ATTTATTTTATTTTA	22937
rs752931110	snp	C/T	1.79149e-05	0.00299285	intron-variant	SCAP	GRCh38.p7	3:47423887	AGGAACAGGCCCCAT[C/T]CCAGCCCCTCCTGCA	22937
rs752932099	snp	A/G	9.82753e-05	0.00700914	synonymous-codon	SCAP	GRCh38.p7	3:47417541	CACCAGGCAGCTGAA[A/G]TCATAGCCTGGGGAG	22937
rs752935216	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47459567	TGAGTAGGACCGTGA[C/T]ACCCACCCGAGCTGC	22937
rs752977168	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47465433	CCAAAGCTATCTACA[A/G]ACGCAATCCATATCA	22937
rs752994133	snp	C/G	5.42559e-05	0.00520817	missense	SCAP	GRCh38.p7	3:47417767	CCACCATCTGAAAGT[C/G]GTTCCCAGCTCTCCT	22937
rs752997710	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47431662	TGCGGTTATGGGTTT[C/G]GGAGAGGAAGATCAG	22937
rs753024481	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47428162	CTTCAGAAGGTACCC[A/C]CAGGTAGAGCTTGCT	22937
rs753025611	snp	C/G	9.92375e-05	0.00704336	intron-variant, synonymous-codon, utr-variant-5-prime	SCAP	GRCh38.p7	3:47428521	GGGGTACCTGTCTCT[C/G]AGCACGTGGTTCCGG	22937
rs753047516	snp	C/T	1.64806e-05	0.00287054	missense	SCAP	GRCh38.p7	3:47415101	AGGCCCTCCGACCTC[C/T]AAACTGCAGGGGGCT	22937
rs753132569	snp	A/G	5.24728e-05	0.00512188	intron-variant	SCAP	GRCh38.p7	3:47435158	ATGTACAAAAAGGAG[A/G]TAAGAATTAGACACT	22937
rs753132633	snp	C/T	1.71381e-05	0.00292724	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47425655	GGCCCCTCCCCCAGC[C/T]CCCGGCCCACTGGGG	22937
rs753142974	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47422889	GCATGTGGTTCTTGT[C/T]TGGTCTGCACGGGCC	22937
rs753149264	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47449322	GGCCCCTTTCCTGGT[C/T]TTCTGGCTAAAAGTC	22937
rs753184105	snp	A/G	4.95536e-05	0.00497738	synonymous-codon, intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47426034	AAACAAGATGATGTA[A/G]GTGGTCACAAGGGGG	22937
rs753208787	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47436276	TTTATACTAGGATCA[C/T]GAGGAAAGTTAAGTT	22937
rs753247957	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47471052	GACATAACTGAGTGA[C/T]AGGTACACAAGGGCT	22937
rs753270012	snp	C/T	2.29014e-05	0.00338381	missense	SCAP	GRCh38.p7	3:47418793	CCCTCCAGAGCCTCC[C/T]TCGGGTTCAGGCGGA	22937
rs753272809	snp	C/T	3.84911e-05	0.00438681	intron-variant	SCAP	GRCh38.p7	3:47415217	CAGGGGCCTCTCCCT[C/T]AGAGCCCCAGCCCTG	22937
rs753279911	snp	A/G	3.3042e-05	0.00406447	downstream-variant-500B, missense	PTPN23, SCAP	GRCh38.p7	3:47413909	CTGAGCTCACTGCCA[A/G]AGTTGCAGACAATGG	22937
rs753305426	snp	C/G	3.98351e-05	0.00446273	intron-variant	SCAP	GRCh38.p7	3:47420532	CCAGAAGAGGGCAGG[C/G]CAGGGCAGGGGTGGC	22937
rs753331407	snp	A/T			intron-variant	SCAP	GRCh38.p7	3:47454457	TTAGGCCAGGCACGG[A/T]GGCTCACACCTGTAA	22937
rs753378863	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47452115	AGAGCCTATTTCTTC[C/T]TTTTCAGTGCATTTA	22937
rs753427155	in-del	-/A	1.65263e-05	0.00287452	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47427129	CCCAGCAGACCAGTC[-/A]AAGAGCCCAGGGTAC	22937
rs753435400	snp	C/G	1.8146e-05	0.00301209	missense	SCAP	GRCh38.p7	3:47417778	AAGTCGTTCCCAGCT[C/G]TCCTGAGCCTCAAGC	22937
rs753470952	snp	C/G	3.52379e-05	0.00419735	intron-variant	SCAP	GRCh38.p7	3:47435162	ACAAAAAGGAGATAA[C/G]AATTAGACACTATGA	22937
rs753474523	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47449997	CTTTGCCTTCAAAGA[A/C]ACTTTTTTTTCTTTT	22937
rs753490442	snp	A/G	2.23786e-05	0.00334497	intron-variant	SCAP	GRCh38.p7	3:47417845	GGGGCCAGGAGGGCG[A/G]AGTGAGAGGGGGCAC	22937
rs753490555	snp	A/G	1.70539e-05	0.00292005	synonymous-codon	SCAP	GRCh38.p7	3:47415120	CTGCAGGGGGCTGAG[A/G]GCAGTGTGGGTCTCC	22937
rs753499366	snp	C/T	1.65004e-05	0.00287227	utr-variant-5-prime, missense	SCAP	GRCh38.p7	3:47442944	CAGAGGAGCCCATGG[C/T]TGTAGAAGGCCCGAG	22937
rs753592633	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47431726	GGGCACAATCAATCA[A/G]TGTGATTTATCACTG	22937
rs753592679	snp	A/C/T	3.30449e-05	0.00406467	missense, intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47426060	GGGGGATGAGCTCAG[A/C/T]GACACCAATCTCCTC	22937
rs753629224	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47428143	AGCACGACTTGGGCT[A/G]GGGCTTCAGAAGGTA	22937
rs753641503	snp	A/G	0.000677507	0.0183928	intron-variant	SCAP	GRCh38.p7	3:47418300	GGCCCTCCCCTACCC[A/G]GCCACTGTGCCCCTG	22937
rs753705770	snp	C/T	1.6501e-05	0.00287232	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47427401	CAAAAAGACGGTGAC[C/T]AATGGGCACCTTTAC	22937
rs753731611	snp	A/G	1.79628e-05	0.00299685	synonymous-codon	SCAP	GRCh38.p7	3:47417430	GGGGGAGCCACCCTC[A/G]TCCTCAGGGGCCTGG	22937
rs753765541	snp	A/G	3.29332e-05	0.00405777	missense	SCAP	GRCh38.p7	3:47417383	GAACCCTCGGCACTG[A/G]GGGCCCAGGCGAGGG	22937
rs753792799	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47473975	GCAAAAGAAAAGAGA[A/G]AGCATTCAAGCCAGG	22937
rs753835125	snp	A/G	1.71299e-05	0.00292654	intron-variant	SCAP	GRCh38.p7	3:47414424	TGGGGTCACCATGGT[A/G]TAATACCTCTGTCAA	22937
rs753896397	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47440710	CCCAGCTCTACTAAA[A/G]ATACAAAAAATTAGT	22937
rs753898025	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47458295	TTAGCTGGGTGTGGT[A/G]GCATGCGTCTGTAAT	22937
rs753913097	in-del	-/AAAAAAAAAAA			intron-variant	SCAP	GRCh38.p7	3:47448017	TCAAAAAAAAAAAAA[-/AAAAAAAAAAA]AAAAAAACTTGATAG	22937
rs753919203	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47438677	AAATTGGCCGGACGC[A/G]GTGGCACACGCCTGT	22937
rs753922563	in-del	-/CAAT			intron-variant	SCAP	GRCh38.p7	3:47433354	AGGGGATGAGCGCTC[-/CAAT]CAGAGAGAGAGGAAA	22937
rs753938805	in-del	-/C	1.71035e-05	0.00292429	frameshift-variant	SCAP	GRCh38.p7	3:47415115	CTAAACTGCAGGGGG[-/C]TGAGGGCAGTGTGGG	22937
rs753941312	snp	C/T	0.000153128	0.00874874	intron-variant	SCAP	GRCh38.p7	3:47418574	ACAGCCTGTCCCCTC[C/T]CCTCCTCCCTCTCCC	22937
rs753957070	in-del	-/CAA			intron-variant	SCAP	GRCh38.p7	3:47424200	CTTGTCCACCTCACC[-/CAA]CAAGACCTGCATCTA	22937
rs753963651	snp	C/T	2.76171e-05	0.00371588	missense	SCAP	GRCh38.p7	3:47417617	GTGGGCTGTGAGGAC[C/T]GAGGCTGCGCTGAAA	22937
rs753990510	snp	C/G	3.32055e-05	0.00407451	intron-variant, synonymous-codon, utr-variant-5-prime	SCAP	GRCh38.p7	3:47428665	AGCCACCGGGGCACC[C/G]ACATACTGCAGAAGA	22937
rs753992550	snp	C/T	6.98544e-05	0.00590951	intron-variant	SCAP	GRCh38.p7	3:47414788	GCTCCCACCCCGTGC[C/T]GGGCCACTCCAGCAC	22937
rs753993581	snp	C/T	1.65097e-05	0.00287308	synonymous-codon, intron-variant	SCAP	GRCh38.p7	3:47424006	GAGCACCAACACATT[C/T]TCTAACCCAATAACC	22937
rs754017523	snp	G/T	1.68043e-05	0.0028986	missense	SCAP	GRCh38.p7	3:47414891	TTCAGGGCTGTGATG[G/T]GTTTTTGGTGTGCAC	22937
rs754056645	snp	C/T	1.65773e-05	0.00287895	missense	SCAP	GRCh38.p7	3:47414059	CCAGTCACCAGCAGG[C/T]TGTCTGAGATGACAC	22937
rs754086806	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47447170	GCACTTTGGGAGACC[A/G]AGGTGGGCGGATCGC	22937
rs754116527	snp	C/T	3.34107e-05	0.00408708	synonymous-codon, intron-variant, utr-variant-5-prime	SCAP	GRCh38.p7	3:47425502	GCCATTGAGGGTGGG[C/T]GTCAGGCCGAAGAGT	22937
rs754184027	snp	C/T	2.01603e-05	0.00317486	intron-variant	SCAP	GRCh38.p7	3:47415230	CTTAGAGCCCCAGCC[C/T]TGGGGCTGAGCATGT	22937
rs754193247	snp	C/G	1.65455e-05	0.00287619	missense	SCAP	GRCh38.p7	3:47414015	GGTCCCCGTAGTTTA[C/G]GTCCCAAAAGGAGAC	22937
rs754214878	in-del	-/CATCAT	1.91782e-05	0.00309657	utr-variant-3-prime, downstream-variant-500B, cds-indel	PTPN23, SCAP	GRCh38.p7	3:47413216	CTGGTCCTTACACTA[-/CATCAT]CATCATCTCATGCCC	22937
rs754228428	snp	C/G	6.98422e-05	0.00590899	intron-variant	SCAP	GRCh38.p7	3:47420543	CAGGGCAGGGCAGGG[C/G]TGGCAGGTACCATGA	22937
rs754355057	snp	A/G	3.3437e-05	0.00408869	synonymous-codon	SCAP	GRCh38.p7	3:47420680	TGTGGACGGCCTCAC[A/G]GCCAGCTGCCGCTCG	22937
rs754358875	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47423166	CCTACAGCCCCATTC[C/T]TCACAGACATGGGGT	22937
rs754367277	snp	A/G			upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47477172	CACAATGAAAGTAAC[A/G]ATGGGGACAGTGGGC	22937
rs754431485	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47446509	TTTTTGTTGTTGTTG[C/T]TCTTCAGTTGGGGTT	22937
rs754447626	snp	C/G	3.29696e-05	0.00406001	intron-variant, missense, upstream-variant-2KB	SCAP	GRCh38.p7	3:47427161	GTCAATCTTACTTGG[C/G]ATGGTAGTGCTGGAA	22937
rs754489042	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47454506	CCAAGGCTGGTGGAT[C/T]GTTTGAGGTCAGGAG	22937
rs754498869	snp	C/G	1.68587e-05	0.00290329	intron-variant	SCAP	GRCh38.p7	3:47420782	TGCTAGCTGTTGGGG[C/G]CACAGTGGTCAGGGC	22937
rs754531613	in-del	-/C	0.000641643	0.0179	intron-variant	SCAP	GRCh38.p7	3:47418607	CTCTTGCCTACCCGT[-/C]CCCCCTCCCCGCACT	22937
rs754532647	snp	C/T	1.66327e-05	0.00288376	missense	SCAP	GRCh38.p7	3:47414248	GGTCATCCAGGCCAC[C/T]GCTGATGACACAGGA	22937
rs754547859	snp	A/G	1.65941e-05	0.00288041	intron-variant	SCAP	GRCh38.p7	3:47414143	CCTGAGTCCTTCCCT[A/G]AAATCCCAAGAATCC	22937
rs754581570	snp	C/T	4.63317e-05	0.00481287	intron-variant	SCAP	GRCh38.p7	3:47418621	GTCCCCCTCCCCGCA[C/T]TCTTTCCCACCCCAC	22937
rs754607672	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47459502	AAATAAAGAGAAACA[A/G]TACAAAGAGAGGAAT	22937
rs754626642	snp	A/G	1.9255e-05	0.00310276	missense	SCAP	GRCh38.p7	3:47417656	TCAATTAAGCAGGTG[A/G]GGTCAGGCTGGTCCC	22937
rs754627886	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47444316	CTCACTGATGAAAAC[C/G]CAGACTCAAAGATGA	22937
rs754655193	in-del	-/C	1.89209e-05	0.00307573	frameshift-variant	SCAP	GRCh38.p7	3:47417669	TGAGGTCAGGCTGGT[-/C]CCCGAAGAGGGAAGG	22937
rs754769886	snp	C/T	3.59945e-05	0.00424217	intron-variant	SCAP	GRCh38.p7	3:47419277	ATTGGGGAAAGGGGA[C/T]GGTGAGTTGACACCA	22937
rs754800003	snp	C/T	1.65364e-05	0.0028754	utr-variant-5-prime, synonymous-codon	SCAP	GRCh38.p7	3:47442973	AGATATCTTCTCACG[C/T]AGCCTTTCAGTCAGG	22937
rs754835219	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47417857	GCGGAGTGAGAGGGG[A/G]CACGGGGGAGGGGGG	22937
rs754850325	snp	G/T			intron-variant	SCAP	GRCh38.p7	3:47456571	AGGAGTTTGAGACCA[G/T]TCTGACCAATATGGC	22937
rs754871670	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47429508	TGTGCACCACCACCA[C/T]GCCTAATTTTCAAAA	22937
rs754889807	snp	A/G	1.70142e-05	0.00291664	utr-variant-5-prime, missense, intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47426153	GCATCAGGCGGGCAC[A/G]CAGGCTGCCCAGGAA	22937
rs754951028	snp	C/T	0.000115721	0.00760572	synonymous-codon	SCAP	GRCh38.p7	3:47418142	CACCTACCCTGGGCG[C/T]GGAATGCGCGTTAGG	22937
rs754966611	snp	C/T	1.81171e-05	0.00300969	missense	SCAP	GRCh38.p7	3:47419649	GCAGCGAGGTAGTTG[C/T]GCAGCCCTGCTGGGT	22937
rs754994272	snp	C/T	5.03918e-05	0.0050193	intron-variant	SCAP	GRCh38.p7	3:47417211	GGCGTCCCACACCTA[C/T]GAGTCCAGAGGCTGT	22937
rs755058883	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47451090	ACTCCTGGTTTCAAG[C/G]AATCCTCCTGCCTCA	22937
rs755081039	snp	C/G	9.89609e-05	0.00703354	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47427411	GTGACCAATGGGCAC[C/G]TTTACAGGTCTGAAG	22937
rs755178502	in-del	-/AA			intron-variant	SCAP	GRCh38.p7	3:47472459	AAAAAAAAATAAAAT[-/AA]AATAATAATAATAAT	22937
rs755179051	snp	A/C	1.70362e-05	0.00291853	missense	SCAP	GRCh38.p7	3:47418386	CATAGCCGTAGTCGT[A/C]GCAGGGCAGCTCCCC	22937
rs755183396	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47463975	CTGCTGGGACTACAG[A/G]CATGAGCCACCACAT	22937
rs755186043	snp	A/T			intron-variant	SCAP	GRCh38.p7	3:47464217	GACGGGGTTTCACCA[A/T]GTTAGTCAGGCTGGT	22937
rs755192723	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47425217	ACACAAACATACCAA[C/T]ACACACCCCTTATAT	22937
rs755208981	snp	G/T	1.64727e-05	0.00286986	intron-variant, missense, upstream-variant-2KB, utr-variant-5-prime	SCAP	GRCh38.p7	3:47427513	TCCCAATGATGTCAG[G/T]ATCAGCATGGAAGCG	22937
rs755320442	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47442862	TATCCAAGGCAACCC[A/C]AAAACATACCAGCAG	22937
rs755329308	snp	C/G	1.67055e-05	0.00289006	intron-variant	SCAP	GRCh38.p7	3:47434916	TTCACAAATCAGAAG[C/G]TGACCAACCTCAATC	22937
rs755393003	snp	A/C/G	5.58897e-05	0.00528604	missense	SCAP	GRCh38.p7	3:47417699	GCGGCGGAGGGCCCC[A/C/G]GGGGCGGTGTCTCAG	22937
rs755417165	snp	C/T	1.68672e-05	0.00290402	missense	SCAP	GRCh38.p7	3:47414930	GTGTGGGTCAGGTGA[C/T]AGGCCACTGTGTCGC	22937
rs755426335	in-del	-/A			intron-variant	SCAP	GRCh38.p7	3:47440159	TTTGGGTTTGGCTGT[-/A]CAAGTCTTTCATCCC	22937
rs755431886	snp	A/G	3.31329e-05	0.00407005	missense, intron-variant, utr-variant-5-prime	SCAP	GRCh38.p7	3:47425554	AGCAGCGAGCTGAGC[A/G]CTGTGACCACGGCAG	22937
rs755478172	snp	A/G	1.76378e-05	0.00296961	intron-variant	SCAP	GRCh38.p7	3:47415006	TCCCTGAGGACAAAA[A/G]GCCAAGTGAAGAATC	22937
rs755480676	snp	C/T	0.000135704	0.0082361	missense	SCAP	GRCh38.p7	3:47419575	GGGGCAGCATGCCAC[C/T]AGGCACGGGCATGGG	22937
rs755528637	snp	C/T			intron-variant, upstream-variant-2KB	SCAP, LOC105377073	GRCh38.p7	3:47474659	AAAATTAGCCGGGCG[C/T]GGTGGCACACACCTG	22937
rs755569052	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47434792	CAGTGAGCCGAGATT[C/G]TGCCATTGCACTCCA	22937
rs755589741	snp	G/T			intron-variant	SCAP	GRCh38.p7	3:47414445	CCTCTGTCAACAGTG[G/T]TGTCCCTGTGCCCCA	22937
rs755622121	snp	C/T	2.10183e-05	0.00324172	missense	SCAP	GRCh38.p7	3:47418700	ACCCCACCTGGGCCC[C/T]TGGGTCCTGCTTCCC	22937
rs755711364	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47447184	CGAGGTGGGCGGATC[A/G]CTTGAGGCCAGGAGT	22937
rs755712527	snp	A/C	1.65833e-05	0.00287948	intron-variant, utr-variant-5-prime	SCAP	GRCh38.p7	3:47434945	TCTCACTGGCAGACC[A/C]CTGCCTCAGCCAGTC	22937
rs755713371	snp	C/G	1.69931e-05	0.00291483	intron-variant	SCAP	GRCh38.p7	3:47414403	TGGGGAAACAGGCCA[C/G]GGGAGTGGGGTCACC	22937
rs755723690	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47469925	TGACCTCTTAGTTCA[C/T]TGCCACAGCTCTACT	22937
rs755728873	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47451987	CCTCTATTCCCTCTT[C/G]TCTTTATAGGCTGGT	22937
rs755734453	in-del	-/A	2.95469e-05	0.00384351	intron-variant	SCAP	GRCh38.p7	3:47418855	TACCTGGATTCGGAC[-/A]AGTGGGCAGCCTCAG	22937
rs755746524	snp	A/G	2.29218e-05	0.00338532	missense	SCAP	GRCh38.p7	3:47418776	CGTCCTGAGGGTGCC[A/G]GCCCTCCAGAGCCTC	22937
rs755762666	snp	C/T	5.56323e-05	0.00527381	missense	SCAP	GRCh38.p7	3:47417704	GGAGGGCCCCGGGGG[C/T]GGTGTCTCAGGGGAG	22937
rs755776032	snp	A/G	1.77511e-05	0.00297913	intron-variant	SCAP	GRCh38.p7	3:47415031	AGAATCTCTGAGAAA[A/G]CAATGGGTAGACGGC	22937
rs755816164	snp	A/G	1.81263e-05	0.00301045	missense	SCAP	GRCh38.p7	3:47417774	CTGAAAGTCGTTCCC[A/G]GCTCTCCTGAGCCTC	22937
rs755826250	in-del	-/C	1.69686e-05	0.00291273	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47425647	ATCAGGGCGGCCCCT[-/C]CCCCAGCCCCCGGCC	22937
rs755888712	snp	A/T	0.000131191	0.00809803	missense	SCAP	GRCh38.p7	3:47418207	GGCCTGCCAGGCAGC[A/T]GCTCACCAGCAGCAT	22937
rs755904997	in-del	-/TA			intron-variant	SCAP	GRCh38.p7	3:47448241	TCACTTTTTAGCAAC[-/TA]TGTTTTCAATTTTGA	22937
rs755966955	snp	A/G			intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47426951	CTACCTTAGTCCCCT[A/G]TGCTTAACCAGCTGT	22937
rs755973042	snp	C/G	1.69057e-05	0.00290733	intron-variant	SCAP	GRCh38.p7	3:47420811	GCCTGAGTCCACCAT[C/G]CAGAGGCTGCTCGCA	22937
rs755990746	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47440684	GACCAGCCTGGGCAA[A/C]ATGGCGAAACCCCAG	22937
rs755999998	snp	G/T	1.69e-05	0.00290684	intron-variant	SCAP	GRCh38.p7	3:47417224	TACGAGTCCAGAGGC[G/T]GTGAGCACCTGCCAG	22937
rs756105237	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47456779	AACAAAGCGAGACTC[C/T]GTCTCAAAAAAAAAA	22937
rs756171828	snp	C/T	7.94486e-05	0.00630222	synonymous-codon	SCAP	GRCh38.p7	3:47417463	CAGCACCGGCCCAGG[C/T]GAGGGTGGGCGCAGG	22937
rs756202449	snp	C/T	6.59e-05	0.00573983	utr-variant-5-prime, missense	SCAP	GRCh38.p7	3:47435042	GGCTCTCCTTGTTTG[C/T]GGTCAGAGTCCACAG	22937
rs756274524	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47451543	GCTAGGACTATAGGC[A/G]TGCACCACCACACCC	22937
rs756295971	snp	A/G	0.000174749	0.00934579	missense	SCAP	GRCh38.p7	3:47417551	CTGAAGTCATAGCCT[A/G]GGGAGTCCCGAGAGC	22937
rs756326407	snp	C/T	1.77931e-05	0.00298266	intron-variant	SCAP	GRCh38.p7	3:47423892	CAGGCCCCATTCCAG[C/T]CCCTCCTGCAGCCCT	22937
rs756350670	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47459390	AAATGGGAGATGTGA[C/T]GAGTCTCGTTGCGTT	22937
rs756353829	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47419198	CCTAAACCACCAGTT[A/C]CCACCTCACAACCTT	22937
rs756362286	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47452469	ACTTCTAACTGTGAT[A/G]CAAAGCACCTCAGGC	22937
rs756389124	snp	A/G	1.66288e-05	0.00288343	intron-variant	SCAP	GRCh38.p7	3:47414704	GATTTTCCAAGTTAT[A/G]CTTTGGCTGGGAAAT	22937
rs756475308	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47460764	GGTTTCACCATCCTG[C/G]CCAGGCTGGTCTTGA	22937
rs756515660	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47444478	TTCCAATCCAGGAAC[A/C]CTTTATTTTTTTTGA	22937
rs756535189	snp	C/T	1.71525e-05	0.00292847	synonymous-codon	SCAP	GRCh38.p7	3:47415108	CCGACCTCTAAACTG[C/T]AGGGGGCTGAGGGCA	22937
rs756540633	in-del	-/A			intron-variant	SCAP	GRCh38.p7	3:47464502	ACTAGAATGAAGGAG[-/A]AAAACAATGATCATC	22937
rs756556941	snp	A/C/G	1.65176e-05	0.00287376	synonymous-codon, intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47426037	CAAGATGATGTAGGT[A/C/G]GTCACAAGGGGGATG	22937
rs756560969	snp	A/G	1.82998e-05	0.00302482	missense	SCAP	GRCh38.p7	3:47419685	TATACCAGGATGCCA[A/G]TCCAGACAACGGTGC	22937
rs756578226	snp	A/T			intron-variant	SCAP	GRCh38.p7	3:47434749	GGCTGAGGCAGGAGA[A/T]TCACTTGAACCCGGG	22937
rs756584166	snp	C/T			upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47476190	GCAGAAAGCCGGGCA[C/T]GGTGGCTCGCGGTTG	22937
rs756588071	snp	A/C	1.65209e-05	0.00287405	downstream-variant-500B, missense	PTPN23, SCAP	GRCh38.p7	3:47413910	TGAGCTCACTGCCAA[A/C]GTTGCAGACAATGGC	22937
rs756610733	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47436394	CCCAACACTTTGGGA[A/G]AGGCCAAGCGGGCGG	22937
rs756639053	snp	C/T	9.7996e-05	0.00699917	missense	SCAP	GRCh38.p7	3:47418350	GCAGCACAAGCGGCA[C/T]GATCTCCGTCTCGGG	22937
rs756673092	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47442538	TGCACTTAACCAGGT[A/G]CTAAAACGAAACCAC	22937
rs756683830	snp	A/G	7.67342e-05	0.00619364	intron-variant	SCAP	GRCh38.p7	3:47420536	AAGAGGGCAGGGCAG[A/G]GCAGGGGTGGCAGGT	22937
rs756712555	snp	G/T			upstream-variant-2KB, utr-variant-5-prime, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47477111	TCCTCCTAAAACCCA[G/T]TTCCCACCGGACTCT	22937
rs756719335	snp	A/G	1.648e-05	0.0028705	utr-variant-5-prime, synonymous-codon	SCAP	GRCh38.p7	3:47435062	AGAGTCCACAGGTGG[A/G]GGCGAGTAATCCTTC	22937
rs756746602	snp	C/T	2.30763e-05	0.00339671	synonymous-codon	SCAP	GRCh38.p7	3:47418795	CTCCAGAGCCTCCCT[C/T]GGGTTCAGGCGGAGC	22937
rs756770428	snp	C/T	9.07894e-05	0.00673695	missense	SCAP	GRCh38.p7	3:47417782	CGTTCCCAGCTCTCC[C/T]GAGCCTCAAGCCCGC	22937
rs756774391	snp	C/T	1.7725e-05	0.00297694	intron-variant	SCAP	GRCh38.p7	3:47435166	AAAGGAGATAAGAAT[C/T]AGACACTATGAGAGG	22937
rs756853676	snp	A/G	4.51248e-05	0.00474978	intron-variant	SCAP	GRCh38.p7	3:47417846	GGGCCAGGAGGGCGG[A/G]GTGAGAGGGGGCACG	22937
rs756896071	in-del	-/A			intron-variant	SCAP	GRCh38.p7	3:47432317	AGACTCCGTCTTGAA[-/A]AAAAAAAAAAAAAAA	22937
rs756897137	snp	A/G	5.10408e-05	0.00505151	missense	SCAP	GRCh38.p7	3:47415130	CTGAGGGCAGTGTGG[A/G]TCTCCAAGGAGAAGA	22937
rs756907204	snp	A/G	1.65214e-05	0.0028741	downstream-variant-500B, synonymous-codon	PTPN23, SCAP	GRCh38.p7	3:47413914	CTCACTGCCAAAGTT[A/G]CAGACAATGGCAGCG	22937
rs756910663	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47443201	GGTTTCAGAATGCCT[A/G]TATGCAAGGTCTAGT	22937
rs756923851	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47416076	CCCACTGGCAGAAAT[C/G]AACATCACTAAGGGC	22937
rs756948514	snp	A/G	1.72039e-05	0.00293285	intron-variant	SCAP	GRCh38.p7	3:47417101	CTGGGGACATCTGGG[A/G]CTGAGGCAGGCCACG	22937
rs756957086	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47471431	GACCCTGGATACAAA[C/G]TTGACTCTGAGCTTC	22937
rs757023566	snp	A/G	1.68581e-05	0.00290324	synonymous-codon	SCAP	GRCh38.p7	3:47417391	GGCACTGGGGGCCCA[A/G]GCGAGGGAAGGGGAG	22937
rs757035241	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47447078	AAAAGACTATCCTTC[C/T]TCCATTGAATTGCTT	22937
rs757059187	snp	A/C/T			intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47426866	GGTGCTCAGTAGTAA[A/C/T]CAGCTGGGGATGCCT	22937
rs757074836	snp	A/G	1.71272e-05	0.00292632	intron-variant	SCAP	GRCh38.p7	3:47414426	GGGTCACCATGGTGT[A/G]ATACCTCTGTCAACA	22937
rs757077468	snp	A/T	1.64953e-05	0.00287182	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47427402	AAAAAGACGGTGACC[A/T]ATGGGCACCTTTACA	22937
rs757094821	in-del	-/GTGGGAAGAGCC	1.64939e-05	0.0028717	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47427275	GTCTGCAAGCAGAAA[-/GTGGGAAGAGCC]CCAGCAGGTACTGAC	22937
rs757113758	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47464081	AGTACAGTGGCATGA[C/T]CTCAGCTCACTGCAA	22937
rs757124008	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47419006	AGGTCCCTCCCCAGC[C/T]CAGCTTAGCAGCCAA	22937
rs757129731	snp	G/T			intron-variant	SCAP	GRCh38.p7	3:47458339	GAGGCTGAGGCAGGA[G/T]AATCGCTTGAACCCT	22937
rs757133959	snp	C/G	2.13072e-05	0.00326392	missense	SCAP	GRCh38.p7	3:47418709	GGGCCCTTGGGTCCT[C/G]CTTCCCAGTGCCCAG	22937
rs757177895	snp	A/G	1.64727e-05	0.00286986	intron-variant, missense, upstream-variant-2KB, utr-variant-5-prime	SCAP	GRCh38.p7	3:47427492	TAGGCTCGTGCTGGT[A/G]GATGGTCCCAATGAT	22937
rs757190588	snp	A/G	1.65315e-05	0.00287498	synonymous-codon	SCAP	GRCh38.p7	3:47422463	GGCGGGCACTAGGGT[A/G]AAGTAGCCGATGAGG	22937
rs757267599	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47442351	GCTCTCACAACTGTC[C/T]TTGGCAAGTGCAGCT	22937
rs757276032	in-del	-/A			intron-variant	SCAP	GRCh38.p7	3:47465842	TTGTTTAAAAAAACA[-/A]AAAAAAAAAAAGCTG	22937
rs757283481	snp	C/T	1.70464e-05	0.0029194	intron-variant	SCAP	GRCh38.p7	3:47423916	CAGCCCTCTGCCCAA[C/T]TCTCCCACTGCGTTA	22937
rs757288302	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47425467	CCTGTGGCCCAGTGG[A/G]GCCTGCTAGGGACCT	22937
rs757342318	snp	C/T	1.65157e-05	0.0028736	missense, intron-variant	SCAP	GRCh38.p7	3:47424013	AACACATTCTCTAAC[C/T]CAATAACCACCACAA	22937
rs757378452	snp	A/G	0.000106358	0.0072916	missense	SCAP	GRCh38.p7	3:47417618	TGGGCTGTGAGGACC[A/G]AGGCTGCGCTGAAAA	22937
rs757403080	in-del	-/TATT			intron-variant, upstream-variant-2KB	SCAP, LOC105377073	GRCh38.p7	3:47474385	ATAAATATGGAAATA[-/TATT]TATACAGTGTTAAAT	22937
rs757457096	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47453575	AGTATTTATAAACCA[C/T]GTGTCAGCCTCTGGC	22937
rs757457934	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47455962	GAACAGAATGTCCAG[A/G]AATAGACCAAAATGT	22937
rs757466264	snp	C/T	4.96602e-05	0.00498274	missense	SCAP	GRCh38.p7	3:47419533	CATCAGGTGGGAAGA[C/T]GGAGAAGGCAGGGTC	22937
rs757482164	snp	A/G			upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47477182	GTAACAATGGGGACA[A/G]TGGGCCTTGGCCCAA	22937
rs757493103	snp	G/T	3.30109e-05	0.00406256	missense	SCAP	GRCh38.p7	3:47419437	TTACCTCTGGGACTG[G/T]GCTGTCATGGACAAC	22937
rs757501731	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47436875	AGCATACCACTCCCC[A/C]CCACCAAAGGTAACT	22937
rs757544896	snp	C/T	0.000108102	0.00735115	missense	SCAP	GRCh38.p7	3:47418147	ACCCTGGGCGCGGAA[C/T]GCGCGTTAGGCAATC	22937
rs757554153	in-del	-/ATAT			intron-variant	SCAP	GRCh38.p7	3:47455063	ATACAAAAAAATTAC[-/ATAT]ATATATATATATATA	22937
rs757591694	snp	A/G	3.33611e-05	0.00408405	missense, intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47426132	AGTTGGGGCTGGGGT[A/G]CAGAAGCATCAGGCG	22937
rs757613619	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47448379	TGTGTGTGGATTCTT[C/T]GGAAATTTCTACGTA	22937
rs757644085	snp	G/T	3.16221e-05	0.00397618	intron-variant	SCAP	GRCh38.p7	3:47420551	GGCAGGGGTGGCAGG[G/T]ACCATGATGAGGCGC	22937
rs757697127	snp	A/G	7.21839e-05	0.00600722	missense	SCAP	GRCh38.p7	3:47418410	GCTCCCCGCGCCTCC[A/G]CCGCCCGGGCCCACC	22937
rs757697824	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47430305	TCTCACTAGAATCTG[C/T]CATCTACCTTTCAAG	22937
rs757711612	snp	A/G	0.000184136	0.00959344	missense	SCAP	GRCh38.p7	3:47420681	GTGGACGGCCTCACA[A/G]CCAGCTGCCGCTCGT	22937
rs757735586	snp	C/G	9.85892e-05	0.00702032	intron-variant	SCAP	GRCh38.p7	3:47427682	GCTGCACAGGAGACA[C/G]GACAAGGCACCTGCT	22937
rs757740492	snp	A/G	7.28783e-05	0.00603605	missense	SCAP	GRCh38.p7	3:47417561	AGCCTGGGGAGTCCC[A/G]AGAGCGGCCACAGAC	22937
rs757768995	in-del	-/ATCA	2.00164e-05	0.00316351	utr-variant-3-prime, downstream-variant-500B	PTPN23, SCAP	GRCh38.p7	3:47413219	TCCTTACACTACATC[-/ATCA]ATCATCATCTCATGC	22937
rs757786734	in-del	-/CG			intron-variant	SCAP	GRCh38.p7	3:47462390	TGTAGTAAAGGCACA[-/CG]CAGTGAAGCCTCCAT	22937
rs757837748	snp	C/T	4.95536e-05	0.00497738	utr-variant-5-prime, missense	SCAP	GRCh38.p7	3:47442963	AGAAGGCCCGAGATA[C/T]CTTCTCACGCAGCCT	22937
rs757837801	snp	A/G	4.96249e-05	0.00498096	synonymous-codon, intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47426088	CTCCTTGAAGTGCAC[A/G]TGGACCAGGCTCTCC	22937
rs757845262	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47432193	GTGGTGGTGCGTGCC[C/T]GTAGTCCCAGCTACT	22937
rs757877568	snp	A/G	0.000138976	0.00833478	intron-variant	SCAP	GRCh38.p7	3:47418113	TGGGGGCACAAAGGA[A/G]GAAAGGGCAGCCGCA	22937
rs757884343	snp	C/T	0.000412335	0.0143526	intron-variant	SCAP	GRCh38.p7	3:47418536	CCCTGCACGGGAGGG[C/T]GGACTGCTGTGAGAC	22937
rs757920492	snp	A/G	3.34622e-05	0.00409023	missense	SCAP	GRCh38.p7	3:47417197	AGCACCCCTTCAATG[A/G]CGTCCCACACCTACG	22937
rs757932573	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47457957	GCTTCAAAATTAGCC[A/G]GTAACCTGGGAGAAT	22937
rs757975902	snp	A/T			intron-variant	SCAP	GRCh38.p7	3:47442489	AAGATACTGTTCTAA[A/T]GGACTTTGCCTCGCA	22937
rs757976509	snp	C/G	3.31367e-05	0.00407029	synonymous-codon	SCAP	GRCh38.p7	3:47414028	TAGGTCCCAAAAGGA[C/G]ACACAGCCCTGGCCG	22937
rs758003682	in-del	-/G	1.74868e-05	0.00295687	intron-variant, utr-variant-3-prime, downstream-variant-500B	PTPN23, SCAP	GRCh38.p7	3:47413804	CAGGTTCAGTGCATT[-/G]GCCCCCACACAGCAC	22937
rs758012972	snp	A/T			intron-variant	SCAP	GRCh38.p7	3:47474154	CCTGTAGTCCCAGCT[A/T]CTTGGGAGGCTGAGG	22937
rs758090248	snp	C/T	3.4647e-05	0.00416201	intron-variant, missense, utr-variant-5-prime	SCAP	GRCh38.p7	3:47427657	ACTCCTCCAAGCTCC[C/T]GATCCCAGAGCTGCA	22937
rs758137388	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47439073	TACGATGGGGTTATG[C/T]CCTGATAACGCTGTC	22937
rs758226685	snp	A/G/T	3.304e-05	0.00406437	synonymous-codon	SCAP	GRCh38.p7	3:47422478	GAAGTAGCCGATGAG[A/G/T]ATGATGCCCAGCTCC	22937
rs758245168	in-del	-/TTA	1.64931e-05	0.00287163	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47427413	GACCAATGGGCACCT[-/TTA]CAGGTCTGAAGGGAA	22937
rs758254271	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47467448	CATCTCCACAAAAAA[C/T]ATGAATATAAGCCAG	22937
rs758263646	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47443857	AAGGTGCCCCGTGCC[A/G]ACCCAAGCTACACAA	22937
rs758283498	snp	A/T	2.28809e-05	0.0033823	missense	SCAP	GRCh38.p7	3:47418799	AGAGCCTCCCTCGGG[A/T]TCAGGCGGAGCGTGA	22937
rs758285583	snp	C/T	3.44786e-05	0.00415188	intron-variant	SCAP	GRCh38.p7	3:47422586	ATGGCCACTCTGCGA[C/T]ATGACTCACACAACC	22937
rs758292119	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47466004	TGGGCGTGGTGGCAG[A/G]TGCCTGTAATATCAA	22937
rs758354869	snp	A/G	1.65261e-05	0.0028745	intron-variant	SCAP	GRCh38.p7	3:47442822	AGGGTTAGAAAACCT[A/G]CTGTCCTAAGACACT	22937
rs758370220	snp	A/G	1.65696e-05	0.00287828	missense, intron-variant, utr-variant-5-prime	SCAP	GRCh38.p7	3:47425545	ACAGACATGAGCAGC[A/G]AGCTGAGCACTGTGA	22937
rs758380109	snp	C/G			intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47426949	CCCTACCTTAGTCCC[C/G]TATGCTTAACCAGCT	22937
rs758395982	snp	A/T			intron-variant	SCAP	GRCh38.p7	3:47458802	TAAGAATCAGTTTTA[A/T]TTTTATTTATTTCTT	22937
rs758398161	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47414488	CTGACTGCTTCCTGG[A/C]AGGCCCCTGGGGACC	22937
rs758399779	snp	G/T	4.2069e-05	0.00458614	intron-variant	SCAP	GRCh38.p7	3:47417854	AGGGCGGAGTGAGAG[G/T]GGGCACGGGGGAGGG	22937
rs758408675	snp	A/G	0.000125389	0.007917	intron-variant	SCAP	GRCh38.p7	3:47418872	GTGGGCAGCCTCAGC[A/G]GGGGGCCTCCCAGGG	22937
rs758423329	in-del	-/A			intron-variant	SCAP	GRCh38.p7	3:47415348	CCAGAGGGCAACTCC[-/A]AATATTAACCACCTT	22937
rs758433285	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47428330	CTGCATAGGTCCAAG[C/T]GGAATGCAGCCACCG	22937
rs758446082	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47462012	GTACTCCAGCCTGGG[C/T]GACAGAGTGAGACTC	22937
rs758490301	snp	A/G	6.68248e-05	0.00577996	missense	SCAP	GRCh38.p7	3:47419550	GAGAAGGCAGGGTCC[A/G]GGTGGCTGGGGGGCA	22937
rs758526306	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47428391	GCTAGCTCACCCTCC[A/G]TCCTTCTTGCTTGTT	22937
rs758579693	snp	A/G	1.75459e-05	0.00296186	missense	SCAP	GRCh38.p7	3:47414990	CTGCCCCGCCCTGGG[A/G]TCCCTGAGGACAAAA	22937
rs758586130	snp	G/T	0.000245387	0.011074	utr-variant-3-prime, downstream-variant-500B	PTPN23, SCAP	GRCh38.p7	3:47413232	ATCATCATCATCTCA[G/T]GCCCACCTGCCCACA	22937
rs758618019	snp	A/G	5.08083e-05	0.00504	synonymous-codon	SCAP	GRCh38.p7	3:47418226	CACCAGCAGCATGCC[A/G]TCGCTGGCCAGGCAC	22937
rs758618115	snp	A/G	1.79146e-05	0.00299282	missense	SCAP	GRCh38.p7	3:47419637	TCCGTCACCTGGGCA[A/G]CGAGGTAGTTGCGCA	22937
rs758642503	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47423516	CTCCCACCTCAGCCT[A/C]TTGAGTAGGTGGGAC	22937
rs758670894	snp	A/C	0.000112682	0.00750523	intron-variant	SCAP	GRCh38.p7	3:47418302	CCCTCCCCTACCCGG[A/C]CACTGTGCCCCTGCT	22937
rs758741382	snp	A/G	1.67987e-05	0.00289811	stop-gained	SCAP	GRCh38.p7	3:47420754	CCTCAGGGGGCAGTC[A/G]CTTGTTCAGGTCTGC	22937
rs758779669	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47433106	GGCTCAAACTATATC[A/G]TGCTTAAGTCAGCCC	22937
rs758784767	in-del	-/G			intron-variant	SCAP	GRCh38.p7	3:47450475	GGAAACGTTAGTAGT[-/G]GTTGCTTGTCTTTGT	22937
rs758809528	snp	A/G	1.67245e-05	0.00289171	intron-variant	SCAP	GRCh38.p7	3:47428695	AAATGAGGGAGGGCA[A/G]AAAGGGCAGCTGAGC	22937
rs758865980	snp	A/G	1.64784e-05	0.00287035	intron-variant, missense, utr-variant-5-prime	SCAP	GRCh38.p7	3:47428564	AGTTGGAATGCCCGG[A/G]ACAAAGGTGAACGAA	22937
rs758881747	snp	A/G	1.68781e-05	0.00290495	intron-variant	SCAP	GRCh38.p7	3:47424049	GGGAAAATCTCGCTG[A/G]GGACAGAGAAGGAGA	22937
rs758924212	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47463551	TACTAAAAATACAAA[A/C]ATTAGCTGGGTGTGG	22937
rs758942424	in-del	-/CTCTGCCCACCTTTAGCCC	1.78492e-05	0.00298735	intron-variant	SCAP	GRCh38.p7	3:47417274	CGGGGCGGACAGCCG[-/CTCTGCCCACCTTTAGCCC]CTCTGCCCACCTTTA	22937
rs758960635	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47448524	ATAAACTTTCTGTTA[C/T]TGTCCCATGGGTCCC	22937
rs758968695	snp	A/T	8.53024e-05	0.00653023	missense	SCAP	GRCh38.p7	3:47417630	ACCGAGGCTGCGCTG[A/T]AAAGTTGGTGTCAAT	22937
rs758984252	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47464407	TAGATATTAAACATA[C/T]ATCTCAGATGACAAG	22937
rs758995833	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47461286	CAAATATTTGGTCAA[A/G]GTCTAAAAAACAAAG	22937
rs759008659	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47416921	GTGAGCCACCGCGCC[C/T]GGCCACCCCTAACGC	22937
rs759024401	snp	A/G	1.70761e-05	0.00292194	intron-variant, utr-variant-3-prime, downstream-variant-500B	PTPN23, SCAP	GRCh38.p7	3:47413831	GCACCCCAGCCTCCT[A/G]CCTGGGCAAGGAGGC	22937
rs759057495	snp	A/T	1.64906e-05	0.00287142	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47427271	AACAAGTCTGCAAGC[A/T]GAAACCAGCAGGTAC	22937
rs759072472	in-del	-/CT			intron-variant	SCAP	GRCh38.p7	3:47458421	GCAACAGGGGCAAAA[-/CT]CTGTCTCAAAAAAAT	22937
rs759136549	snp	A/G	8.75021e-05	0.00661388	intron-variant	SCAP	GRCh38.p7	3:47418285	TATGGGCCAGGCTCC[A/G]GCCCTCCCCTACCCG	22937
rs759168890	snp	A/G	0.000101148	0.00711082	missense	SCAP	GRCh38.p7	3:47418152	GGGCGCGGAATGCGC[A/G]TTAGGCAATCCCCGG	22937
rs759190351	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47460266	CTCAGCTTACGAAGA[C/T]AACAGGATTAAGAGA	22937
rs759211135	snp	C/T	2.53181e-05	0.00355786	missense	SCAP	GRCh38.p7	3:47417366	GCTCCAAGCTCCAGA[C/T]GGAACCCTCGGCACT	22937
rs759217970	snp	C/T	1.64735e-05	0.00286993	intron-variant, missense, upstream-variant-2KB, utr-variant-5-prime	SCAP	GRCh38.p7	3:47427483	GCAGGGTTTTAGGCT[C/T]GTGCTGGTGGATGGT	22937
rs759228707	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47470460	AGTGAACATCTGTAC[A/G]CAGGAGTTAACACCC	22937
rs759254234	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47438220	TTGAATATTTTAAAT[A/C]CATTTATTATGTTAA	22937
rs759255886	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47421759	CTGCTCACCCCCATC[C/T]CTCAGCTGGCCTGCC	22937
rs759274160	snp	C/T	1.65603e-05	0.00287747	intron-variant, synonymous-codon, utr-variant-5-prime	SCAP	GRCh38.p7	3:47428656	CTGGACATAAGCCAC[C/T]GGGGCACCCACATAC	22937
rs759289295	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47460243	GTGGTCCTGAGGTGA[C/T]GTACATCCTCAGCTT	22937
rs759298649	snp	C/G	1.68193e-05	0.00289989	missense	SCAP	GRCh38.p7	3:47414887	GGCTTTCAGGGCTGT[C/G]ATGGGTTTTTGGTGT	22937
rs759305791	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47415404	ATGGGGATAAGAGTA[C/T]CCACCTCACAGGGTG	22937
rs759333589	snp	A/G	7.8416e-05	0.00626114	missense	SCAP	GRCh38.p7	3:47417416	GGGGAGCCTTTCTCG[A/G]GGGAGCCACCCTCGT	22937
rs759375315	snp	C/T	3.43637e-05	0.00414496	intron-variant	SCAP	GRCh38.p7	3:47425474	CCCAGTGGAGCCTGC[C/T]AGGGACCTACCCGCC	22937
rs759401951	snp	A/C/G	3.7361e-05	0.00432196	missense	SCAP	GRCh38.p7	3:47417678	GCTGGTCCCCGAAGA[A/C/G]GGAAGGCGGCGGAGG	22937
rs759407087	snp	C/T	1.71832e-05	0.00293109	missense	SCAP	GRCh38.p7	3:47414958	CGCTGCTGCTGTACA[C/T]TGGAGAGGCAGGGGA	22937
rs759428603	snp	C/T	1.76412e-05	0.0029699	missense	SCAP	GRCh38.p7	3:47419623	CCAATGGGCTCTGTT[C/T]CGTCACCTGGGCAGC	22937
rs759435251	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47447862	AAATACAAAATAGCC[A/G]GGCATGGTGGCGTGT	22937
rs759452433	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47470702	ATCCCATCTACTAAA[A/G]GTACAAAAACTAGCC	22937
rs759486756	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47449387	CCACAACTGTGACTA[A/C]CTCCAAGGAAAAGCA	22937
rs759501653	snp	C/G	1.65113e-05	0.00287322	missense	SCAP	GRCh38.p7	3:47419509	TCTGGTTCTCAGGTA[C/G]CTTAGGGGCATCAGG	22937
rs759528100	in-del	-/A			intron-variant	SCAP	GRCh38.p7	3:47462753	GCGAAACTCCGTCTC[-/A]AAAAAAAAAAAAAAA	22937
rs759533837	snp	C/G	9.08405e-05	0.00673884	utr-variant-3-prime, downstream-variant-500B	PTPN23, SCAP	GRCh38.p7	3:47413204	GGTTTTGCCTACCTG[C/G]TCCTTACACTACATC	22937
rs759591628	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47427973	GCCAGTTCAGTGGAT[A/G]AGCAGGGACCGGGGT	22937
rs759610017	snp	A/C/G	6.61227e-05	0.00574957	synonymous-codon, intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47426016	GGAGAAGTAGATGTA[A/C/G]GCAAACAAGATGATG	22937
rs759636321	snp	C/G	1.64901e-05	0.00287137	utr-variant-5-prime, synonymous-codon	SCAP	GRCh38.p7	3:47442901	GCAGAACCCTGTGAA[C/G]AGGATGATGGGGATG	22937
rs759662085	snp	C/G	0.000117028	0.00764856	synonymous-codon	SCAP	GRCh38.p7	3:47420656	CGGCTGCAACGTGAT[C/G]GTGTGGGGTGTGGAC	22937
rs759708115	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47465225	ACCCAGGCTGGAGTG[C/T]AGTGGCACAATCTCG	22937
rs759837124	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47442243	CAGATGTCATCTCAT[A/G]TCAAACTCCTCCTTT	22937
rs759837135	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47459204	GAGTGTCCTCAGCCT[C/T]CACTCCAGCAGGTAC	22937
rs759843483	snp	A/G	1.65787e-05	0.00287907	synonymous-codon	SCAP	GRCh38.p7	3:47414085	GACACCCAAGCTTGC[A/G]CCACAGCCCAGGTCC	22937
rs759895000	snp	C/T	1.80824e-05	0.0030068	synonymous-codon	SCAP	GRCh38.p7	3:47417760	AGCCTTCCCACCATC[C/T]GAAAGTCGTTCCCAG	22937
rs759898079	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47454312	GACGGAGCCTGCAGT[A/G]AGCAGAGATCACGCC	22937
rs759918726	snp	A/T			intron-variant	SCAP	GRCh38.p7	3:47435785	TGGGCGCAGTGGGTT[A/T]TGCCTGTAACCCCAG	22937
rs759921710	snp	A/G	5.00471e-05	0.00500211	synonymous-codon, utr-variant-5-prime	SCAP	GRCh38.p7	3:47422534	AGCTCTCGCTGCTTA[A/G]GCCTGCAGAGGGCAG	22937
rs759923583	in-del	-/GCA	1.67688e-05	0.00289554	intron-variant	SCAP	GRCh38.p7	3:47422545	TTAGGCCTGCAGAGG[-/GCA]GCAGCAACAGGGCAC	22937
rs759945763	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47428842	TAAGAAAAGAAACAA[C/T]TTGCTGAAACCCAGA	22937
rs759975187	snp	A/G	0.000145504	0.00852824	synonymous-codon	SCAP	GRCh38.p7	3:47418825	CGTGACTGGGATGAC[A/G]GGCAGCAGGCTGATG	22937
rs760017591	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47448890	CTGATTTTTCATAGC[C/T]GAAGTAATTCTGAAT	22937
rs760054433	snp	A/T	3.29451e-05	0.00405851	intron-variant, missense, upstream-variant-2KB, utr-variant-5-prime	SCAP	GRCh38.p7	3:47427485	AGGGTTTTAGGCTCG[A/T]GCTGGTGGATGGTCC	22937
rs760056381	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47449630	ATGAGGATCCCCTTT[C/T]CTGCTCCTCAAACTA	22937
rs760077721	in-del	-/AT			intron-variant	SCAP	GRCh38.p7	3:47435467	ATATATAATATAAAC[-/AT]ATACACACACACACA	22937
rs760099348	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47434433	TGACTGAGCCCCTCA[A/G]CTGAAGACCTTTTTT	22937
rs760105190	snp	C/T	1.70356e-05	0.00291848	intron-variant	SCAP	GRCh38.p7	3:47422413	AGTTGCTTCCATGCT[C/T]ATCCAGGTGGCAGGC	22937
rs760149510	snp	A/G	1.98797e-05	0.00315269	intron-variant	SCAP	GRCh38.p7	3:47417830	CGGCGCTGCCTGCTG[A/G]GGGCCAGGAGGGCGG	22937
rs760235273	snp	A/T	1.64852e-05	0.00287094	intron-variant, missense, utr-variant-5-prime	SCAP	GRCh38.p7	3:47427606	GGTTCCTGAGCTTCC[A/T]AAGGCCTGGCAGCAG	22937
rs760290855	snp	C/T	1.77325e-05	0.00297758	missense	SCAP	GRCh38.p7	3:47417425	TTCTCGGGGGAGCCA[C/T]CCTCGTCCTCAGGGG	22937
rs760305750	snp	A/T			intron-variant	SCAP	GRCh38.p7	3:47454240	GGCGAGGTGGCGGGC[A/T]CCTGTAGTCCCAGCT	22937
rs760342147	snp	C/T	1.65894e-05	0.00288	missense	SCAP	GRCh38.p7	3:47414580	CGCTTACCTGGTCAA[C/T]GTACACGGTCGTGAT	22937
rs760357260	snp	C/T	2.64044e-05	0.00363339	synonymous-codon	SCAP	GRCh38.p7	3:47418843	CAGCAGGCTGATGTA[C/T]CTGGATTCGGACAGT	22937
rs760359863	snp	A/T	1.68482e-05	0.00290238	intron-variant	SCAP	GRCh38.p7	3:47422552	CTGCAGAGGGCAGCA[A/T]CAGGGCACAGGGCAA	22937
rs760430965	snp	C/T	2.00164e-05	0.00316351	utr-variant-3-prime, downstream-variant-500B	PTPN23, SCAP	GRCh38.p7	3:47413219	GTCCTTACACTACAT[C/T]ATCATCATCTCATGC	22937
rs760436501	snp	A/G			intron-variant, upstream-variant-2KB	SCAP, LOC105377073	GRCh38.p7	3:47475292	TAAACCCACTCAGAA[A/G]TAAACAGAAGCAACA	22937
rs760527333	snp	C/G	3.54742e-05	0.00421139	synonymous-codon	SCAP	GRCh38.p7	3:47419627	TGGGCTCTGTTCCGT[C/G]ACCTGGGCAGCGAGG	22937
rs760585816	in-del	-/CCTCTGCCCCATCAGCTATACAA			intron-variant	SCAP	GRCh38.p7	3:47462330	ACAGTCATCTGACAG[-/CCTCTGCCCCATCAGCTATACAA]CCTCTGCCCCATCGG	22937
rs760598759	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47432785	TGGGCTCAAGCGATC[C/T]TCCTGCCTCAGTACT	22937
rs760653790	snp	G/T			intron-variant	SCAP	GRCh38.p7	3:47418081	CGTGGCGGCGGGGGG[G/T]GGGGTGAGGGGGGTT	22937
rs760653799	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47434102	GTTGTGCCACAGACC[C/T]ATCTTGCCAGATATG	22937
rs760674994	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47470811	AGGTTGCAGTGAGCC[A/G]AGATCGCACCACTGC	22937
rs760676491	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47430826	GAGGGGCTGTCTCCA[C/T]GCCTGGGCTGCAGTC	22937
rs760685789	snp	G/T			synonymous-codon	SCAP	GRCh38.p7	3:47415162	ATCAAGGGAACCGTT[G/T]AGCCGTGCAGCCACA	22937
rs760699669	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47473954	GGGGGCGTTTTTGCC[A/G]CAACAGCAAAAGAAA	22937
rs760714956	in-del	-/T			intron-variant	SCAP	GRCh38.p7	3:47446008	AGCCTCCTGAGTAGC[-/T]GGAATTACAGATGCG	22937
rs760746234	snp	C/T	1.69761e-05	0.00291337	intron-variant	SCAP	GRCh38.p7	3:47418558	CTGTGAGACACACCT[C/T]ACAGCCTGTCCCCTC	22937
rs760756238	snp	A/G	1.6607e-05	0.00288153	missense	SCAP	GRCh38.p7	3:47414197	GCTGAATGGAGTAGA[A/G]CTTGATGCCTGTGCT	22937
rs760796692	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47453320	GGCTGAGATGGGAGG[A/C]TTGCTTGAGCCCAGA	22937
rs760808778	in-del	-/GGGGGGT	8.44987e-05	0.0064994	intron-variant	SCAP	GRCh38.p7	3:47417867	AGGGGGCACGGGGGA[-/GGGGGGT]GAGAGGGGGCGGGGG	22937
rs760837280	snp	A/G	4.16675e-05	0.00456421	missense	SCAP	GRCh38.p7	3:47418461	GCGGGCATAGCACGC[A/G]GTAGAGGCAGAGCAG	22937
rs760853834	snp	A/G	4.95143e-05	0.00497541	intron-variant, synonymous-codon, utr-variant-5-prime	SCAP	GRCh38.p7	3:47428527	CCTGTCTCTCAGCAC[A/G]TGGTTCCGGATCTCC	22937
rs760858625	in-del	-/G	1.66103e-05	0.00288182	intron-variant	SCAP	GRCh38.p7	3:47414661	GGAACACCTGGGACA[-/G]GGATGGGCCTCAGGT	22937
rs760865363	snp	A/G	6.6855e-05	0.00578126	missense	SCAP	GRCh38.p7	3:47420714	CGCGTTGGCTGTCCC[A/G]CTGGCTTGGCTGAGG	22937
rs760867030	snp	A/G	1.66355e-05	0.002884	missense	SCAP	GRCh38.p7	3:47417605	GGCTCGGGCTGAGTG[A/G]GCTGTGAGGACCGAG	22937
rs760881215	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47423107	CCAGCACAGGGCCTG[A/G]CTTATCACAGAGGCT	22937
rs761001660	snp	C/T	0.000477969	0.0154517	intron-variant	SCAP	GRCh38.p7	3:47418650	ACCCCACCCAGCAGC[C/T]TTACTTGTACAGCGT	22937
rs761062264	snp	A/G	0.000267049	0.0115522	intron-variant	SCAP	GRCh38.p7	3:47419311	AGTGAGGTGGCACCT[A/G]GCACGGCCCAGCTCA	22937
rs761062735	snp	C/T	2.18279e-05	0.00330355	intron-variant	SCAP	GRCh38.p7	3:47417843	TGGGGGCCAGGAGGG[C/T]GGAGTGAGAGGGGGC	22937
rs761115851	snp	A/G	0.000160424	0.00895466	intron-variant	SCAP	GRCh38.p7	3:47418089	CGGGGGGTGGGGTGA[A/G]GGGGGTTGTGGGGGC	22937
rs761162141	snp	C/T			upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47478110	AGAGGGTCAGGAGCC[C/T]GTCTTTTAACCACCT	22937
rs761196193	snp	A/G/T	9.97567e-05	0.00706187	intron-variant	SCAP	GRCh38.p7	3:47414681	GGGCCTCAGGTTCTG[A/G/T]TCTCTGGGATTTTCC	22937
rs761237117	snp	A/C/G	8.92215e-05	0.00667863	intron-variant	SCAP	GRCh38.p7	3:47418857	ACCTGGATTCGGACA[A/C/G]TGGGCAGCCTCAGCG	22937
rs761238914	snp	C/G	1.6666e-05	0.00288664	utr-variant-5-prime	SCAP	GRCh38.p7	3:47443033	CATCCCGGAAAGTGA[C/G]CATGGATCACCCTGG	22937
rs761258283	snp	A/G	6.63306e-05	0.00575855	missense, intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47426108	CCAGGCTCTCCGCCC[A/G]AAGGCTGCAGTTGGG	22937
rs761273984	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47474041	GAGGCCGAAGCGGAC[A/G]GATCATGAGGTCAGG	22937
rs761309541	snp	C/T	0.000100294	0.00708075	synonymous-codon	SCAP	GRCh38.p7	3:47420671	GGTGTGGGGTGTGGA[C/T]GGCCTCACAGCCAGC	22937
rs761311468	snp	A/G	7.03788e-05	0.00593165	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47426221	TGCTCTTGGTTCTGG[A/G]GACAAAGACAATCCC	22937
rs761362229	snp	C/T	1.68519e-05	0.0029027	intron-variant	SCAP	GRCh38.p7	3:47428492	GGGATTCAGGGAGGC[C/T]AGGGTCCCTGAGAGG	22937
rs761362356	snp	A/G	1.69752e-05	0.0029133	intron-variant	SCAP	GRCh38.p7	3:47422571	GGCACAGGGCAACAC[A/G]TGGCCACTCTGCGAC	22937
rs761372739	in-del	-/AT			intron-variant	SCAP	GRCh38.p7	3:47468991	ACATTCTGGAAATGG[-/AT]AGTGATGATGGTTGC	22937
rs761468205	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47459938	AGACACTCCCAGAGC[A/G]GCCATTTATAGACCT	22937
rs761479734	snp	A/G	1.72943e-05	0.00294055	synonymous-codon	SCAP	GRCh38.p7	3:47414839	CACTCTCAGTGTGTG[A/G]TCTTGGCTCCCAGTC	22937
rs761523075	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47450075	TGATCTCGGCTCACC[A/G]CAACCTCCGCCTCCT	22937
rs761550698	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47464581	ATTAAAAAATACTCA[A/G]TGAAATAGGAATAGA	22937
rs761628679	snp	C/T	5.02113e-05	0.0050103	synonymous-codon	SCAP	GRCh38.p7	3:47420650	GGAAGACGGCTGCAA[C/T]GTGATGGTGTGGGGT	22937
rs761628759	snp	A/G	8.37346e-05	0.00646995	synonymous-codon	SCAP	GRCh38.p7	3:47418378	GGGTGGCGCATAGCC[A/G]TAGTCGTCGCAGGGC	22937
rs761649767	snp	C/T	1.65165e-05	0.00287367	missense	SCAP	GRCh38.p7	3:47413967	GGGCAGGCTGGGCCT[C/T]ACTGTTCTTCCCCAG	22937
rs761681586	snp	A/G	9.54608e-05	0.00690806	missense	SCAP	GRCh38.p7	3:47418446	GCTGCCCGTAGTTGC[A/G]CGGGCATAGCACGCG	22937
rs761713487	snp	C/T	1.75068e-05	0.00295857	synonymous-codon	SCAP	GRCh38.p7	3:47417520	CTCCTCCTGGTACAC[C/T]CGCTGCACCAGGCAG	22937
rs761799094	snp	C/G			intron-variant, utr-variant-5-prime, upstream-variant-2KB	SCAP, LOC105377073	GRCh38.p7	3:47475454	TCCGGAAAACCCAAA[C/G]AGCACCAAAGCAGGT	22937
rs761817049	snp	G/T			intron-variant	SCAP	GRCh38.p7	3:47459380	TCAAATCCCAAAATG[G/T]GAGATGTGACGAGTC	22937
rs761870471	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47462957	TGACTCCTGGCTCCA[A/G]TTCTCATCTGTTTGC	22937
rs761894432	snp	C/G	1.66399e-05	0.00288438	intron-variant	SCAP	GRCh38.p7	3:47428674	GGCACCCACATACTG[C/G]AGAAGAAATGAGGGA	22937
rs761901210	snp	A/T			intron-variant	SCAP	GRCh38.p7	3:47457159	CAAAACACCTGGGAA[A/T]GGACACATGAGAAGT	22937
rs761925914	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47469591	CTTGAACTTCTGACC[C/T]CAAGTGATCCACCCA	22937
rs761930390	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47430430	ACAGCAGAGTTATGG[A/C]CCAGGAGAAGCTGAG	22937
rs761986296	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47441646	AACATACTGAGCCAG[A/C]GTGAAACCAGGTGAC	22937
rs761986595	snp	C/G			upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47478233	TTTGCAGAGGACTGA[C/G]CCTCAGTGAAGTCTG	22937
rs761992534	snp	C/T	1.65059e-05	0.00287275	intron-variant, utr-variant-5-prime	SCAP	GRCh38.p7	3:47434972	AGTCTCCACCCAACG[C/T]TCTGTGCTGGCCTCA	22937
rs761995577	snp	A/C/G	8.7417e-05	0.00661073	missense	SCAP	GRCh38.p7	3:47414982	CAGGGGAACTGCCCC[A/C/G]CCCTGGGGTCCCTGA	22937
rs762016927	snp	A/G	4.99488e-05	0.00499719	synonymous-codon, intron-variant, utr-variant-5-prime	SCAP	GRCh38.p7	3:47425511	GGTGGGCGTCAGGCC[A/G]AAGAGTGTGCAGAGT	22937
rs762025454	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47455705	TCTTAATGAGGAAAA[C/G]TCAATATAACGTAAC	22937
rs762057428	snp	A/G	9.31558e-05	0.00682417	missense	SCAP	GRCh38.p7	3:47417686	CCGAAGAGGGAAGGC[A/G]GCGGAGGGCCCCGGG	22937
rs762085961	in-del	-/GGGGGCGGGGGACGGGG	0.000464576	0.0152339	intron-variant	SCAP	GRCh38.p7	3:47417878	GGGAGGGGGGTGAGA[-/GGGGGCGGGGGACGGGG]GTGAGAGGGGGCGTG	22937
rs762107973	snp	A/G	0.000340686	0.0130471	missense	SCAP	GRCh38.p7	3:47418173	CAATCCCCGGTCTGC[A/G]CGTCCCACACGCAGA	22937
rs762114410	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47414102	CACAGCCCAGGTCCT[A/G]GAGGCAAGGACATGA	22937
rs762126071	snp	C/T	1.67267e-05	0.0028919	utr-variant-5-prime	SCAP	GRCh38.p7	3:47443043	AGTGACCATGGATCA[C/T]CCTGGCACACACTTG	22937
rs762182225	snp	A/C/T	7.30519e-05	0.00604329	synonymous-codon	SCAP	GRCh38.p7	3:47417727	CAGGGGAGGGCTGTC[A/C/T]CCAGGCTCCTCTGGA	22937
rs762195281	snp	A/G	3.34146e-05	0.00408732	synonymous-codon	SCAP	GRCh38.p7	3:47417172	GGAGACCTCCTCGCT[A/G]CTGCAGCACAGCACC	22937
rs762209014	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47458010	TATTGAAAAAAGGTC[A/G]GGCACGGTGGCTCAC	22937
rs762248753	snp	A/G	1.65869e-05	0.00287979	intron-variant	SCAP	GRCh38.p7	3:47414120	GGCAAGGACATGACA[A/G]GCTCAGTCCTGAGTC	22937
rs762275286	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47440157	CCTTTGGGTTTGGCT[A/G]TACAAGTCTTTCATC	22937
rs762277779	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47424735	CTCAGGAAAGGGAGC[A/G]GGTATCTAAGAGCAA	22937
rs762278129	in-del	-/GAG	3.34294e-05	0.00408823	cds-indel	SCAP	GRCh38.p7	3:47417155	AGAGCGGTAATGCCT[-/GAG]GAGACCTCCTCGCTG	22937
rs762319178	snp	G/T			intron-variant	SCAP	GRCh38.p7	3:47463417	CTCAAAACACTCCAG[G/T]GGGCCGGGGTGCGGT	22937
rs762373132	snp	C/T	1.66095e-05	0.00288175	synonymous-codon	SCAP	GRCh38.p7	3:47414207	GTAGAACTTGATGCC[C/T]GTGCTGCGGTCCCAG	22937
rs762378697	snp	A/C	1.6477e-05	0.00287024	intron-variant, missense, upstream-variant-2KB, utr-variant-5-prime	SCAP	GRCh38.p7	3:47427232	TAGAGGCTCACCCCG[A/C]TGTACTTCCCAGGAA	22937
rs762408827	snp	A/G	1.67396e-05	0.00289301	synonymous-codon	SCAP	GRCh38.p7	3:47420728	CACTGGCTTGGCTGA[A/G]GGCAGGCAGGCCTCA	22937
rs762424330	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47460480	TTATGTTCCTCTGCC[A/G]CGGCTCCAGCCAGTC	22937
rs762436067	snp	C/G	6.61091e-05	0.00574893	intron-variant	SCAP	GRCh38.p7	3:47420910	AGGAGGCGGGCAGGG[C/G]AGGGCTCAGCCCACT	22937
rs762463972	snp	C/T	1.69329e-05	0.00290967	intron-variant	SCAP	GRCh38.p7	3:47418605	CTACTCTTGCCTACC[C/T]GTCCCCCTCCCCGCA	22937
rs762496099	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47459408	GTCTCGTTGCGTTAC[C/T]ACTTCAATATTAGGG	22937
rs762550857	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47422005	GCGTCTGGCGACTGC[A/G]GCACAGGCCAGGGCC	22937
rs762550939	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47462557	AAACGCCTACAACCA[C/T]CCTGGCTAACACGGT	22937
rs762565424	snp	A/T	1.64939e-05	0.0028717	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47427150	CCCAGGGTACTGTCA[A/T]TCTTACTTGGCATGG	22937
rs762607828	snp	A/C	1.69215e-05	0.00290869	missense	SCAP	GRCh38.p7	3:47418183	TCTGCGCGTCCCACA[A/C]GCAGACGTGGCCTGC	22937
rs762612485	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47447643	CAGTGAGCCAAAGAC[C/T]GTGCCATTGCACTCC	22937
rs762620496	snp	A/T			intron-variant	SCAP	GRCh38.p7	3:47441150	CGTGATCTGCCCGCC[A/T]CGGCCTCCCAAAGTG	22937
rs762627993	snp	C/G	1.79155e-05	0.0029929	utr-variant-3-prime, downstream-variant-500B	PTPN23, SCAP	GRCh38.p7	3:47413195	ACCTGAACAGGTTTT[C/G]CCTACCTGGTCCTTA	22937
rs762630509	in-del	-/C			intron-variant	SCAP	GRCh38.p7	3:47472774	CACTACCCTTACCTG[-/C]CAATGAGCAACAGAA	22937
rs762692726	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47434566	TAACTGGCCAGGTGC[A/G]GTGGCTCACGCCTGT	22937
rs762724444	snp	A/G	1.76649e-05	0.00297189	intron-variant	SCAP	GRCh38.p7	3:47417266	CACAATCCCCGGGGC[A/G]GACAGCCGCTCTGCC	22937
rs762770534	snp	C/T	1.73462e-05	0.00294496	missense	SCAP	GRCh38.p7	3:47417524	TCCTGGTACACCCGC[C/T]GCACCAGGCAGCTGA	22937
rs762827179	snp	A/T	6.33613e-05	0.0056282	intron-variant	SCAP	GRCh38.p7	3:47418546	GAGGGCGGACTGCTG[A/T]GAGACACACCTCACA	22937
rs762832069	in-del	-/CT	9.96231e-05	0.00705703	intron-variant	SCAP	GRCh38.p7	3:47414537	AACATGGGCCACAGA[-/CT]CTGTACCCCCTACCC	22937
rs762847342	in-del	-/TT			intron-variant	SCAP	GRCh38.p7	3:47451396	AGTCCTGGAATGCCT[-/TT]TTTTTTTTTTTTTTT	22937
rs762958521	snp	C/G	1.65965e-05	0.00288062	utr-variant-5-prime, missense	SCAP	GRCh38.p7	3:47435113	AGGTCCTGTTCCTGG[C/G]AAGGGGAGTTTCAGC	22937
rs763045579	snp	A/T			intron-variant	SCAP	GRCh38.p7	3:47442027	ATCTTTCTTACTGAT[A/T]ATCAGGGAAGAGCTT	22937
rs763049838	snp	C/T	3.29582e-05	0.00405931	intron-variant, utr-variant-5-prime	SCAP	GRCh38.p7	3:47434997	GCCTCAGGAACATGA[C/T]GAGTACCCACCCACT	22937
rs763069429	snp	G/T	1.84049e-05	0.00303349	synonymous-codon	SCAP	GRCh38.p7	3:47417715	GGGGCGGTGTCTCAG[G/T]GGAGGGCTGTCCCCA	22937
rs763077421	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47457484	CACCCAGCACCTCAC[C/G]TGGTGCTGAGCAGAA	22937
rs763085440	snp	A/G	1.65605e-05	0.0028775	synonymous-codon, intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47426004	GAACCTACGCGTGGA[A/G]AAGTAGATGTAGGCA	22937
rs763094476	snp	G/T			intron-variant	SCAP	GRCh38.p7	3:47440329	GAAAAGCTTCAGTGG[G/T]TTGAAGACAATGGTG	22937
rs763108443	snp	A/G	6.74809e-05	0.00580826	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47425640	AGGGCGTATCAGGGC[A/G]GCCCCTCCCCCAGCC	22937
rs763154886	snp	A/G	1.65477e-05	0.00287638	downstream-variant-500B, missense	PTPN23, SCAP	GRCh38.p7	3:47413876	AGCTTCTCCAGCACA[A/G]AGGGCACATACACCA	22937
rs763156621	snp	C/T	5.44144e-05	0.00521577	missense	SCAP	GRCh38.p7	3:47417744	CAGGCTCCTCTGGAC[C/T]AGCCTTCCCACCATC	22937
rs763163983	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47470840	GCACTCCAGCCTGGG[A/C]GACAAGAGCAAGACT	22937
rs763198090	snp	A/C/G	6.01297e-05	0.00548287	missense, synonymous-codon	SCAP	GRCh38.p7	3:47417334	GCTCCGCCCCACCAC[A/C/G]ATGAGGTTGCCCTGC	22937
rs763211255	snp	C/G	1.88025e-05	0.00306609	intron-variant	SCAP	GRCh38.p7	3:47419749	AGGAATGGGCCCCAA[C/G]CCCCAGCAGCTTCAG	22937
rs763211699	snp	A/C	3.49125e-05	0.00417792	intron-variant	SCAP	GRCh38.p7	3:47415081	TGTGAACACCTGCCC[A/C]CCCCAGGCCCTCCGA	22937
rs763257244	snp	C/T	1.648e-05	0.0028705	intron-variant, missense, upstream-variant-2KB, utr-variant-5-prime	SCAP	GRCh38.p7	3:47427248	TGTACTTCCCAGGAA[C/T]ACCAAATAACAAGTC	22937
rs763273706	snp	A/G	1.6625e-05	0.00288309	missense	SCAP	GRCh38.p7	3:47414233	CCCAGATGCTGATGA[A/G]GTCATCCAGGCCACT	22937
rs763324640	snp	A/T			intron-variant	SCAP	GRCh38.p7	3:47466687	AAACTGTAAAGCCCT[A/T]AGAAGAAAATATAAG	22937
rs763355897	snp	G/T	1.65187e-05	0.00287386	missense	SCAP	GRCh38.p7	3:47418677	GCGTGACGTCTCCAT[G/T]GGCCTGCACCCCACC	22937
rs763358297	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47452273	ATGCACCTATAATCC[C/T]GGCTACTCAGGAGAC	22937
rs763383031	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47450291	GTGTGAGCCACTGCT[C/T]CTGGCCCTAAGGAAA	22937
rs763416054	in-del	-/G	0.000116119	0.00761879	intron-variant	SCAP	GRCh38.p7	3:47421052	AGAGCACATGGGGAT[-/G]GGGGGGGTGCCGTGA	22937
rs763495586	snp	C/T			intron-variant, synonymous-codon, utr-variant-5-prime	SCAP	GRCh38.p7	3:47427640	GGTCACTTGCAGACA[C/T]AACTCCTCCAAGCTC	22937
rs763504764	snp	A/G	3.31967e-05	0.00407397	intron-variant	SCAP	GRCh38.p7	3:47421064	GGATGGGGGGGTGCC[A/G]TGACCTCACTGTCCC	22937
rs763518187	snp	G/T			intron-variant	SCAP	GRCh38.p7	3:47454090	AAGAATAGACAGGCC[G/T]GGTGCGGTGGCTCAT	22937
rs763542203	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47460506	CAGTCCCTCCGTTCG[A/G]GGTCCCTGACTTCCC	22937
rs763555923	snp	A/G	6.75641e-05	0.00581184	intron-variant	SCAP	GRCh38.p7	3:47422562	CAGCAACAGGGCACA[A/G]GGCAACACATGGCCA	22937
rs763598735	snp	A/G	3.3173e-05	0.00407252	synonymous-codon	SCAP	GRCh38.p7	3:47422448	GGGCCTTACCTGGAT[A/G]GCGGGCACTAGGGTG	22937
rs763603487	snp	A/G	1.86621e-05	0.00305462	missense	SCAP	GRCh38.p7	3:47417692	AGGGAAGGCGGCGGA[A/G]GGCCCCGGGGGCGGT	22937
rs763611933	in-del	-/CGCCCGG	7.09648e-05	0.00595629	frameshift-variant	SCAP	GRCh38.p7	3:47418412	TCCCCGCGCCTCCGC[-/CGCCCGG]GCCCACCACCCAGCT	22937
rs763644731	snp	C/T	1.71126e-05	0.00292506	intron-variant	SCAP	GRCh38.p7	3:47414423	GTGGGGTCACCATGG[C/T]GTAATACCTCTGTCA	22937
rs763656444	snp	C/T	4.58453e-05	0.00478754	missense	SCAP	GRCh38.p7	3:47418791	GGCCCTCCAGAGCCT[C/T]CCTCGGGTTCAGGCG	22937
rs763679910	snp	C/T	2.82068e-05	0.00375534	intron-variant	SCAP	GRCh38.p7	3:47418851	TGATGTACCTGGATT[C/T]GGACAGTGGGCAGCC	22937
rs763697731	snp	A/G	3.31785e-05	0.00407286	synonymous-codon	SCAP	GRCh38.p7	3:47414581	GCTTACCTGGTCAAT[A/G]TACACGGTCGTGATG	22937
rs763737898	in-del	-/TTGCTC	2.07205e-05	0.00321866	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47426205	GGGTAAATGGAAGTG[-/TTGCTC]TTGGTTCTGGGGACA	22937
rs763755265	snp	A/G	1.74833e-05	0.00295658	intron-variant	SCAP	GRCh38.p7	3:47415077	CAAGTGTGAACACCT[A/G]CCCACCCCAGGCCCT	22937
rs763821801	snp	C/T	1.78093e-05	0.00298401	synonymous-codon	SCAP	GRCh38.p7	3:47419630	GCTCTGTTCCGTCAC[C/T]TGGGCAGCGAGGTAG	22937
rs763889051	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47473962	TTTTGCCGCAACAGC[A/G]AAAGAAAAGAGAGAG	22937
rs763905007	snp	A/G	3.28618e-05	0.00405337	synonymous-codon	SCAP	GRCh38.p7	3:47417382	GGAACCCTCGGCACT[A/G]GGGGCCCAGGCGAGG	22937
rs763906158	snp	C/T	1.87187e-05	0.00305925	utr-variant-3-prime, downstream-variant-500B	PTPN23, SCAP	GRCh38.p7	3:47413227	ACTACATCATCATCA[C/T]CTCATGCCCACCTGC	22937
rs763953908	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47458259	ACACAGTGAAACCCC[A/G]TCTCTACTCAAAAAC	22937
rs763970860	snp	C/T			missense	SCAP	GRCh38.p7	3:47418177	CCCCGGTCTGCGCGT[C/T]CCACACGCAGACGTG	22937
rs764036113	snp	A/C/T	3.31742e-05	0.00407262	intron-variant	SCAP	GRCh38.p7	3:47414118	GAGGCAAGGACATGA[A/C/T]AAGCTCAGTCCTGAG	22937
rs764041601	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47442255	CATATCAAACTCCTC[C/T]TTTACGACGTCATTG	22937
rs764128272	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47436532	CCAGCTACTGGCTGA[C/G]GCAGGAGGATCATCT	22937
rs764129088	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47469424	TGGAGTGCTGTGACA[C/T]GATCCTGGCTCACTG	22937
rs764150829	snp	G/T	0.000249138	0.0111583	missense	SCAP	GRCh38.p7	3:47417554	AAGTCATAGCCTGGG[G/T]AGTCCCGAGAGCGGC	22937
rs764156241	snp	A/C/T	0.000131776	0.00811621	intron-variant, missense, upstream-variant-2KB, utr-variant-5-prime	SCAP	GRCh38.p7	3:47427491	TTAGGCTCGTGCTGG[A/C/T]GGATGGTCCCAATGA	22937
rs764200831	snp	C/G	1.67136e-05	0.00289076	missense	SCAP	GRCh38.p7	3:47420718	TTGGCTGTCCCACTG[C/G]CTTGGCTGAGGGCAG	22937
rs764214394	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47437357	GGCAGGAAAATCACT[C/T]GAACCGGTGAGCTGA	22937
rs764289267	snp	A/G	7.64789e-05	0.00618333	intron-variant	SCAP	GRCh38.p7	3:47418566	CACACCTCACAGCCT[A/G]TCCCCTCCCCTCCTC	22937
rs764329443	snp	A/G	1.65605e-05	0.0028775	intron-variant, missense, utr-variant-5-prime	SCAP	GRCh38.p7	3:47428657	TGGACATAAGCCACC[A/G]GGGCACCCACATACT	22937
rs764342489	snp	C/G	3.16121e-05	0.00397555	missense	SCAP	GRCh38.p7	3:47417609	CGGGCTGAGTGGGCT[C/G]TGAGGACCGAGGCTG	22937
rs764362625	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47428981	ACTGCCATGTTTCAT[A/G]CTAACTCCCCCCGGA	22937
rs764369418	in-del	-/A	5.1632e-05	0.00508068	frameshift-variant	SCAP	GRCh38.p7	3:47414961	GCTGCTGTACACTGG[-/A]AGAGGCAGGGGAACT	22937
rs764380507	snp	A/G	6.7178e-05	0.00579521	intron-variant	SCAP	GRCh38.p7	3:47417844	GGGGGCCAGGAGGGC[A/G]GAGTGAGAGGGGGCA	22937
rs764383957	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47461677	TCCCAGCCCGGGGAA[C/G]ATTTCCATGACAGAG	22937
rs764403993	snp	C/G	1.65072e-05	0.00287286	missense, intron-variant	SCAP	GRCh38.p7	3:47423996	CAGACTTGGTGAGCA[C/G]CAACACATTCTCTAA	22937
rs764408743	in-del	-/CAT	0.000492975	0.0156922	utr-variant-3-prime, downstream-variant-500B	PTPN23, SCAP	GRCh38.p7	3:47413215	CTGGTCCTTACACTA[-/CAT]CATCATCATCATCTC	22937
rs764501334	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47450754	ATCCTCCTGCCTCAA[C/T]TTCCCAAACTGATTA	22937
rs764503183	snp	A/G	2.801e-05	0.00374222	intron-variant	SCAP	GRCh38.p7	3:47418091	GGGGGTGGGGTGAGG[A/G]GGGTTGTGGGGGCAC	22937
rs764504264	snp	A/G	3.29957e-05	0.00406162	utr-variant-5-prime, synonymous-codon	SCAP	GRCh38.p7	3:47442940	TGCACAGAGGAGCCC[A/G]TGGTTGTAGAAGGCC	22937
rs764540288	snp	C/G	1.65154e-05	0.00287358	missense, intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47426045	TGTAGGTGGTCACAA[C/G]GGGGATGAGCTCAGC	22937
rs764550461	snp	G/T			upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47478114	GGTCAGGAGCCTGTC[G/T]TTTAACCACCTCCAT	22937
rs764560230	snp	A/T	3.34191e-05	0.0040876	missense	SCAP	GRCh38.p7	3:47417164	ATGCCTGAGGAGACC[A/T]CCTCGCTGCTGCAGC	22937
rs764562678	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47454236	GCCGGGCGAGGTGGC[A/G]GGCACCTGTAGTCCC	22937
rs764613682	in-del	-/GA			intron-variant	SCAP	GRCh38.p7	3:47419139	CTGGCAGCCACCAGT[-/GA]CTCCTCAGAGCAACC	22937
rs764639012	snp	A/T	1.65416e-05	0.00287586	synonymous-codon	SCAP	GRCh38.p7	3:47414013	CAGGTCCCCGTAGTT[A/T]AGGTCCCAAAAGGAG	22937
rs764678419	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47454556	ACAAGGTGAAACCCC[C/T]GTCTCCACTAAAAAA	22937
rs764681298	snp	A/C/T	9.92103e-05	0.00704247	downstream-variant-500B, synonymous-codon	PTPN23, SCAP	GRCh38.p7	3:47413887	CACAGAGGGCACATA[A/C/T]ACCAGGCTGAGCTCA	22937
rs764717980	snp	A/G	1.67122e-05	0.00289064	missense	SCAP	GRCh38.p7	3:47420672	GTGTGGGGTGTGGAC[A/G]GCCTCACAGCCAGCT	22937
rs764720864	snp	C/T	1.70429e-05	0.0029191	missense	SCAP	GRCh38.p7	3:47419346	TTGGCCAGTGTGATG[C/T]TGTAATAGCTGAAGA	22937
rs764748824	snp	A/T			upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47477158	CACCACACTATTGTC[A/T]CAATGAAAGTAACAA	22937
rs764757346	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47432992	CACTGGATTGGATGA[C/T]GCAAAAACATGGGGC	22937
rs764776012	snp	A/G	2.34211e-05	0.00342199	intron-variant	SCAP	GRCh38.p7	3:47418102	GAGGGGGGTTGTGGG[A/G]GCACAAAGGAGGAAA	22937
rs764804395	snp	C/T	1.67464e-05	0.0028936	missense, intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47426139	GCTGGGGTGCAGAAG[C/T]ATCAGGCGGGCACGC	22937
rs764858166	snp	A/C	2.56644e-05	0.00358211	intron-variant	SCAP	GRCh38.p7	3:47417850	CAGGAGGGCGGAGTG[A/C]GAGGGGGCACGGGGG	22937
rs764868638	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47420036	TGCTACCATTCCTAC[A/G]GTCAGAGGGCCAGCA	22937
rs764875284	snp	C/T	1.67318e-05	0.00289234	utr-variant-5-prime	SCAP	GRCh38.p7	3:47443044	GTGACCATGGATCAC[C/T]CTGGCACACACTTGA	22937
rs764919099	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47443654	ACATAATGGTCACCA[A/G]GCAAAATTCACTCTG	22937
rs764958206	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47434392	CTCCAAATAATGAGT[A/G]CGGTGTGATGGTGAG	22937
rs765009239	snp	C/G	0.000129879	0.00805744	missense	SCAP	GRCh38.p7	3:47417444	CGTCCTCAGGGGCCT[C/G]GGACAGCACCGGCCC	22937
rs765046298	snp	G/T			intron-variant	SCAP	GRCh38.p7	3:47459386	CCCAAAATGGGAGAT[G/T]TGACGAGTCTCGTTG	22937
rs765062530	snp	A/G	3.31862e-05	0.00407333	synonymous-codon	SCAP	GRCh38.p7	3:47414587	CTGGTCAATGTACAC[A/G]GTCGTGATGGCCCCT	22937
rs765126976	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47436159	AAACAAAAGTGGGGG[C/T]ACCTTTAAAAATCCA	22937
rs765199964	snp	C/T	0.0010627	0.0230265	missense	SCAP	GRCh38.p7	3:47417521	TCCTCCTGGTACACC[C/T]GCTGCACCAGGCAGC	22937
rs765209544	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47457252	TTCCCATGTAGTTTA[C/T]CTTTCCAATTTTGTG	22937
rs765217827	snp	A/G	1.66471e-05	0.00288501	intron-variant	SCAP	GRCh38.p7	3:47428675	GCACCCACATACTGC[A/G]GAAGAAATGAGGGAG	22937
rs765238586	snp	C/T			upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47478237	CAGAGGACTGACCCT[C/T]AGTGAAGTCTGGACA	22937
rs765300857	snp	C/T	3.40153e-05	0.0041239	intron-variant	SCAP	GRCh38.p7	3:47422572	GCACAGGGCAACACA[C/T]GGCCACTCTGCGACA	22937
rs765332632	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47470668	AGGAGTTCAAGACTA[C/G]CCTGGCCAACATGGT	22937
rs765343510	snp	C/T	4.47347e-05	0.0047292	missense	SCAP	GRCh38.p7	3:47418665	CTTACTTGTACAGCG[C/T]GACGTCTCCATGGGC	22937
rs765343915	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47423305	AGCTTTTCTGGCAGC[C/T]GTGAAGGCAGCGTCT	22937
rs765344606	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47467184	GGGAGAAACTATTCA[C/G]AAATCATATATCTAA	22937
rs765347825	snp	A/C	2.59683e-05	0.00360326	synonymous-codon	SCAP	GRCh38.p7	3:47417619	GGGCTGTGAGGACCG[A/C]GGCTGCGCTGAAAAG	22937
rs765352248	snp	C/T	1.65855e-05	0.00287967	missense, intron-variant, utr-variant-5-prime	SCAP	GRCh38.p7	3:47425535	GCAGAGTCCCACAGA[C/T]ATGAGCAGCGAGCTG	22937
rs765408326	snp	A/G	1.64985e-05	0.0028721	intron-variant, utr-variant-5-prime	SCAP	GRCh38.p7	3:47434976	TCCACCCAACGCTCT[A/G]TGCTGGCCTCAGGAA	22937
rs765451229	in-del	-/T			intron-variant	SCAP	GRCh38.p7	3:47434264	TTCCTCAACAACAGA[-/T]TCAGCAAGTCCAGCA	22937
rs765451791	in-del	-/AAAAAAAAAAAG			upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47477571	GCGAGACTCCGTCTC[-/AAAAAAAAAAAG]AAAAAAAAAAAGAAA	22937
rs765459142	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47455755	CATTCATCTAGAAAT[C/G]TAACAGTCCCAATAA	22937
rs765477220	snp	C/G	1.86138e-05	0.00305067	missense	SCAP	GRCh38.p7	3:47417687	CGAAGAGGGAAGGCG[C/G]CGGAGGGCCCCGGGG	22937
rs765477644	snp	C/T	1.66632e-05	0.0028864	missense	SCAP	GRCh38.p7	3:47419547	ATGGAGAAGGCAGGG[C/T]CCGGGTGGCTGGGGG	22937
rs765518688	in-del	-/T			intron-variant	SCAP	GRCh38.p7	3:47451397	GTCCTGGAATGCCTT[-/T]TTTTTTTTTTTTTTT	22937
rs765531867	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47446556	TTTTGTTTTCTTTTG[A/C]GTATATTCATTCTTA	22937
rs765534780	snp	A/G	1.67089e-05	0.00289035	synonymous-codon	SCAP	GRCh38.p7	3:47417178	CTCCTCGCTGCTGCA[A/G]CACAGCACCCCTTCA	22937
rs765536460	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47415214	TGCCAGGGGCCTCTC[A/C]CTTAGAGCCCCAGCC	22937
rs765589857	snp	C/T	1.65877e-05	0.00287986	intron-variant	SCAP	GRCh38.p7	3:47414124	AGGACATGACAAGCT[C/T]AGTCCTGAGTCCTTC	22937
rs765621637	snp	A/G	1.64982e-05	0.00287208	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47427146	AGAGCCCAGGGTACT[A/G]TCAATCTTACTTGGC	22937
rs765645431	in-del	-/ACGA	8.39285e-05	0.00647744	splice-acceptor-variant	SCAP	GRCh38.p7	3:47417209	TGGCGTCCCACACCT[-/ACGA]ACGAGTCCAGAGGCT	22937
rs765676999	snp	C/T	1.67663e-05	0.00289532	synonymous-codon	SCAP	GRCh38.p7	3:47420740	TGAGGGCAGGCAGGC[C/T]TCAGGGGGCAGTCGC	22937
rs765689274	in-del	-/CGCCT			intron-variant	SCAP	GRCh38.p7	3:47474003	AGGCGCGGTGGCTCA[-/CGCCT]GTAATCCCAGCACTT	22937
rs765716914	snp	A/T	1.66167e-05	0.00288237	missense	SCAP	GRCh38.p7	3:47414217	ATGCCTGTGCTGCGG[A/T]CCCAGATGCTGATGA	22937
rs765735498	in-del	-/G	0.0016297	0.028499	intron-variant	SCAP	GRCh38.p7	3:47418089	CGGGGGGTGGGGTGA[-/G]GGGGGTTGTGGGGGC	22937
rs765843524	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47459467	TTCTTTCTATTTTCC[A/G]TAAGTGTCGGCCGGC	22937
rs765869950	snp	C/T	5.62509e-05	0.00530304	intron-variant	SCAP	GRCh38.p7	3:47418608	CTCTTGCCTACCCGT[C/T]CCCCTCCCCGCACTC	22937
rs765904028	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47420211	CCAGTGTCTGCACAC[C/T]ATGCAGCGGCCGATG	22937
rs765920903	snp	A/G	0.000270673	0.0116303	intron-variant	SCAP	GRCh38.p7	3:47418119	CACAAAGGAGGAAAG[A/G]GCAGCCGCACCTACC	22937
rs765920943	snp	A/G	1.65048e-05	0.00287265	synonymous-codon	SCAP	GRCh38.p7	3:47419498	GCCTGGCGACGTCTG[A/G]TTCTCAGGTAGCTTA	22937
rs765925928	snp	A/T	1.64931e-05	0.00287163	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47427151	CCAGGGTACTGTCAA[A/T]CTTACTTGGCATGGT	22937
rs765931599	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47460144	CTTGTTCCCTAAAAT[A/G]GCTGTTATTCTGTTT	22937
rs765971437	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47443892	GGCCTCTCTCCCTGG[A/G]CTTTGACTTCTAAAC	22937
rs765981772	snp	C/T	3.34767e-05	0.00409112	missense	SCAP	GRCh38.p7	3:47417198	GCACCCCTTCAATGG[C/T]GTCCCACACCTACGA	22937
rs766051905	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47454304	CCCCGGGGGACGGAG[A/C]CTGCAGTGAGCAGAG	22937
rs766054422	snp	A/G	1.64814e-05	0.00287061	intron-variant, missense, upstream-variant-2KB, utr-variant-5-prime	SCAP	GRCh38.p7	3:47427254	TCCCAGGAACACCAA[A/G]TAACAAGTCTGCAAG	22937
rs766071726	snp	A/G	3.33361e-05	0.00408252	intron-variant	SCAP	GRCh38.p7	3:47428506	CCAGGGTCCCTGAGA[A/G]GGGTACCTGTCTCTC	22937
rs766083738	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47435722	ACTTTTACTGAAAGG[A/C]AACACCAACATGTTA	22937
rs766085910	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47467561	AGTCAACTGTGATTG[C/T]GCCACTGCAGTCTGG	22937
rs766115624	snp	A/C	0.000359346	0.0133994	missense	SCAP	GRCh38.p7	3:47417533	ACCCGCTGCACCAGG[A/C]AGCTGAAGTCATAGC	22937
rs766124980	snp	C/T	3.3042e-05	0.00406447	synonymous-codon, intron-variant	SCAP	GRCh38.p7	3:47423967	CACCTCCAGGTCTAC[C/T]GGGGTTGAGACCACA	22937
rs766167044	snp	C/G	1.66316e-05	0.00288367	intron-variant	SCAP	GRCh38.p7	3:47414696	GTCTCTGGGATTTTC[C/G]AAGTTATACTTTGGC	22937
rs766168592	snp	C/T	4.10467e-05	0.00453008	missense	SCAP	GRCh38.p7	3:47417594	CCCGGTGCCGGGGCT[C/T]GGGCTGAGTGGGCTG	22937
rs766182543	snp	A/G	0.00033089	0.0128583	synonymous-codon	SCAP	GRCh38.p7	3:47414016	GTCCCCGTAGTTTAG[A/G]TCCCAAAAGGAGACA	22937
rs766207583	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47469611	TGATCCACCCACCTT[A/G]GCCTCCCAAAGTGCT	22937
rs766227840	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47463219	ACAAGCCCACATCTG[A/C]AACAGCTGGTTACAA	22937
rs766228453	in-del	-/TG			intron-variant	SCAP	GRCh38.p7	3:47448356	CAGAGTCTTTCTGCA[-/TG]TGTGTGTGTGTGTGG	22937
rs766243663	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47429177	TTTGAGCTGGACTCC[A/G]GTCTCCTAGGGAGTC	22937
rs766266902	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47430459	AGTAGAGCCATAAGG[C/T]TAGAAAAGAACAGGT	22937
rs766283000	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47466811	AACTTTTGGCCGGGC[A/G]TGGTGGCTCACGCCT	22937
rs766321275	snp	C/G	1.80853e-05	0.00300705	missense	SCAP	GRCh38.p7	3:47417755	GGACCAGCCTTCCCA[C/G]CATCTGAAAGTCGTT	22937
rs766360156	snp	C/T	1.69395e-05	0.00291024	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47425645	GTATCAGGGCGGCCC[C/T]TCCCCCAGCCCCCGG	22937
rs766382131	in-del	-/AAAAAAAAAAAA			intron-variant	SCAP	GRCh38.p7	3:47437425	TGAAACTCAATCTCA[-/AAAAAAAAAAAA]AAAAAAAAAAGGAGA	22937
rs766410963	in-del	-/GGGCAACAGA			intron-variant	SCAP	GRCh38.p7	3:47438794	AGTGCACTCTAGCCT[-/GGGCAACAGA]GGGAGACCCTGTCTC	22937
rs766432662	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47446119	GACCTCGTGATCTGA[C/T]CGCCTCAGCCTCCCA	22937
rs766434561	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47473173	ATCTCAGTTTGCACA[C/T]AACACACTCCGTCTC	22937
rs766439708	snp	A/G			intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47426173	CTGCCCAGGAACCTG[A/G]TCAAGGAGCAGGGTG	22937
rs766472360	snp	A/T	1.66004e-05	0.00288096	utr-variant-5-prime, stop-gained	SCAP	GRCh38.p7	3:47435114	GGTCCTGTTCCTGGC[A/T]AGGGGAGTTTCAGCA	22937
rs766486734	snp	C/T	1.79499e-05	0.00299577	missense	SCAP	GRCh38.p7	3:47419638	CCGTCACCTGGGCAG[C/T]GAGGTAGTTGCGCAG	22937
rs766516833	snp	C/T	8.78542e-05	0.00662717	synonymous-codon	SCAP	GRCh38.p7	3:47414992	GCCCCGCCCTGGGGT[C/T]CCTGAGGACAAAAGG	22937
rs766524322	snp	C/T	1.65518e-05	0.00287674	missense, intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47426008	CTACGCGTGGAGAAG[C/T]AGATGTAGGCAAACA	22937
rs766528178	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47442135	TCTATAAATGTTTTA[A/G]ACAATGAATCTGAAG	22937
rs766553117	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47440419	ATTCTCTTATACAAC[A/C]TTTTATTAGTCTTTG	22937
rs766605455	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47425125	CAAGCTGCAGTGTGT[A/G]TGTGGTGTGTGTATA	22937
rs766611578	snp	C/T	0.00010528	0.00725457	missense	SCAP	GRCh38.p7	3:47418332	TCACCATGAGGTGGC[C/T]GCGCAGCACAAGCGG	22937
rs766613246	snp	A/C	1.88503e-05	0.00306998	intron-variant	SCAP	GRCh38.p7	3:47419754	TGGGCCCCAACCCCC[A/C]GCAGCTTCAGCCCTC	22937
rs766614320	snp	A/G	1.65438e-05	0.00287605	downstream-variant-500B, synonymous-codon	PTPN23, SCAP	GRCh38.p7	3:47413878	CTTCTCCAGCACAGA[A/G]GGCACATACACCAGG	22937
rs766639316	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47458190	GTAATCCCAGCACTT[C/T]GGGAGGCCAAGGCGG	22937
rs766751950	snp	A/G	3.30327e-05	0.0040639	synonymous-codon	SCAP	GRCh38.p7	3:47413968	GGCAGGCTGGGCCTC[A/G]CTGTTCTTCCCCAGG	22937
rs766772790	in-del	-/A			intron-variant	SCAP	GRCh38.p7	3:47437576	TGAAACGCCATCCCT[-/A]AAAAAAAAAAAATAC	22937
rs766773480	snp	A/G	1.65633e-05	0.00287774	missense	SCAP	GRCh38.p7	3:47418751	CCCGGTGGGGGCCAG[A/G]CACTGCGGCCGTCCT	22937
rs766784193	snp	C/G	3.34605e-05	0.00409012	synonymous-codon	SCAP	GRCh38.p7	3:47414351	ATCCCACAGGCAGAT[C/G]GCCCCATCTTGTCCT	22937
rs766803939	snp	A/C/G	3.29567e-05	0.00405924	intron-variant, utr-variant-5-prime	SCAP	GRCh38.p7	3:47434998	CCTCAGGAACATGAC[A/C/G]AGTACCCACCCACTC	22937
rs766827344	in-del	-/T			intron-variant	SCAP	GRCh38.p7	3:47473485	TGGTTTGAAGGATGA[-/T]CCACCCTTGACAAGC	22937
rs766835027	snp	A/G	0.000148156	0.00860558	missense	SCAP	GRCh38.p7	3:47418685	TCTCCATGGGCCTGC[A/G]CCCCACCTGGGCCCT	22937
rs766865787	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47465094	AACTGAAACATTGCT[A/G]AAACAAATTAAAGAC	22937
rs766890714	in-del	-/CCCAC	4.40898e-05	0.00469499	intron-variant	SCAP	GRCh38.p7	3:47418627	CTCCCCGCACTCTTT[-/CCCAC]CCCACCCCACCCAGC	22937
rs766893932	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47434575	AGGTGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC	22937
rs766906645	in-del	-/AGC	0.000118537	0.0076977	cds-indel	SCAP	GRCh38.p7	3:47418471	ACGCGGTAGAGGCAG[-/AGC]AGCAGCAGCAGCACC	22937
rs766906826	snp	C/T			upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47478854	CTTGGCTCACTGCAA[C/T]CTCCACCTCTCAGGT	22937
rs766912672	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47453124	GAACTGGACTAGTGA[C/T]AGATATCCAAAACCA	22937
rs766951275	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47450900	CTGTCACCCAGGCTG[C/G]GGTACAGTGGCACTA	22937
rs766972801	snp	A/C/G	4.94176e-05	0.00497059	intron-variant, missense, synonymous-codon, upstream-variant-2KB, utr-variant-5-prime	SCAP	GRCh38.p7	3:47427484	CAGGGTTTTAGGCTC[A/C/G]TGCTGGTGGATGGTC	22937
rs767035759	snp	C/T	1.65168e-05	0.00287369	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47427298	GTACTGACACAGAAA[C/T]GACAGCTACTGCAGA	22937
rs767052967	snp	C/T	1.64947e-05	0.00287177	missense	SCAP	GRCh38.p7	3:47420960	TGTCAATGGACAGGA[C/T]AGTGGTGAAAAACAG	22937
rs767057163	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47429935	TTGCAGCAGAGTAGC[A/G]GGTTTTGAAGATCAA	22937
rs767066659	snp	C/G	3.36417e-05	0.00410119	missense	SCAP	GRCh38.p7	3:47414380	CTCCACTGGCCAGCA[C/G]CATGGTCTGGGGAAA	22937
rs767071650	in-del	-/CAGT			intron-variant	SCAP	GRCh38.p7	3:47473212	TAGGTGACCCAGGGC[-/CAGT]CAAATAACTTTTCTA	22937
rs767092316	snp	C/G	1.75299e-05	0.00296051	intron-variant	SCAP	GRCh38.p7	3:47418289	GGCCAGGCTCCGGCC[C/G]TCCCCTACCCGGCCA	22937
rs767097022	in-del	-/GTA	1.65385e-05	0.00287558	cds-indel, intron-variant	SCAP	GRCh38.p7	3:47424030	AATAACCACCACAAG[-/GTA]GGGGAAAATCTCGCT	22937
rs767143530	snp	C/T	2.77704e-05	0.00372618	synonymous-codon	SCAP	GRCh38.p7	3:47417373	GCTCCAGATGGAACC[C/T]TCGGCACTGGGGGCC	22937
rs767158825	snp	C/G	1.67103e-05	0.00289048	missense, intron-variant, utr-variant-5-prime	SCAP	GRCh38.p7	3:47425501	CGCCATTGAGGGTGG[C/G]CGTCAGGCCGAAGAG	22937
rs767179539	snp	C/G	1.70673e-05	0.00292119	intron-variant	SCAP	GRCh38.p7	3:47422399	CTGGGGAGCACAGCA[C/G]TTGCTTCCATGCTCA	22937
rs767218076	snp	G/T	1.74339e-05	0.0029524	missense	SCAP	GRCh38.p7	3:47414976	GAGAGGCAGGGGAAC[G/T]GCCCCGCCCTGGGGT	22937
rs767248971	snp	C/T	1.68122e-05	0.00289928	missense	SCAP	GRCh38.p7	3:47414889	CTTTCAGGGCTGTGA[C/T]GGGTTTTTGGTGTGC	22937
rs767279116	snp	A/C	1.6519e-05	0.00287388	synonymous-codon	SCAP	GRCh38.p7	3:47419513	GTTCTCAGGTAGCTT[A/C]GGGGCATCAGGTGGG	22937
rs767365424	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47415474	TGGTGAATATCACGT[A/G]AGTTTGTAAATTAAA	22937
rs767388649	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47470775	CTGAGGCAGGAGAGT[C/T]GCTTGAACCCAGGGG	22937
rs767427147	snp	C/T	1.825e-05	0.00302071	utr-variant-3-prime, downstream-variant-500B	PTPN23, SCAP	GRCh38.p7	3:47413206	TTTTGCCTACCTGGT[C/T]CTTACACTACATCAT	22937
rs767436635	snp	A/C	4.54887e-05	0.00476888	intron-variant	SCAP	GRCh38.p7	3:47420513	GGCCTGGAGCACCGG[A/C]CCTCCAGAAGAGGGC	22937
rs767457353	snp	C/G	5.6272e-05	0.00530404	intron-variant	SCAP	GRCh38.p7	3:47415207	GAACAGCTGCCAGGG[C/G]CCTCTCCCTTAGAGC	22937
rs767509839	in-del	-/C			intron-variant	SCAP	GRCh38.p7	3:47446539	TTTTGTATTTTTTTT[-/C]TTTTTGTTTTCTTTT	22937
rs767510530	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47452443	GACAGTGCTCAGTAC[A/G]TATCTTCTCAACTTC	22937
rs767537702	snp	G/T	3.38862e-05	0.00411606	synonymous-codon	SCAP	GRCh38.p7	3:47418193	CCACACGCAGACGTG[G/T]CCTGCCAGGCAGCAG	22937
rs767582370	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47465355	TTTGTATTGTTAGTA[A/G]AGACAGGGTTTCACC	22937
rs767600790	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47466934	TAAAAAAAAATAAAT[A/G]CAAAAAAAATTAGCC	22937
rs767664832	snp	C/T	3.3066e-05	0.00406595	downstream-variant-500B, synonymous-codon	PTPN23, SCAP	GRCh38.p7	3:47413890	AGAGGGCACATACAC[C/T]AGGCTGAGCTCACTG	22937
rs767719888	snp	C/G	1.65266e-05	0.00287455	missense	SCAP	GRCh38.p7	3:47413994	CCAGGTAGACTGTCT[C/G]TAACAGGTCCCCGTA	22937
rs767736525	snp	C/T			intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47426403	GTCTCCCTTTCCGGA[C/T]CTACTCCAACACTCT	22937
rs767756854	snp	C/T	4.2811e-05	0.00462641	missense	SCAP	GRCh38.p7	3:47418458	TGCGCGGGCATAGCA[C/T]GCGGTAGAGGCAGAG	22937
rs767799241	snp	A/G	6.83582e-05	0.00584589	missense	SCAP	GRCh38.p7	3:47418758	GGGGCCAGGCACTGC[A/G]GCCGTCCTGAGGGTG	22937
rs767891154	snp	A/G	2.00543e-05	0.00316651	intron-variant	SCAP	GRCh38.p7	3:47417832	GCGCTGCCTGCTGGG[A/G]GCCAGGAGGGCGGAG	22937
rs767963843	in-del	-/AGGGC			intron-variant	SCAP	GRCh38.p7	3:47420524	CCGGCCCTCCAGAAG[-/AGGGC]AGGGCAGGGCAGGGG	22937
rs767983511	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47473692	CATTCACATGCATGG[A/C]TAGATTCTGAGAGAG	22937
rs767994630	snp	A/G	5.42304e-05	0.00520694	missense	SCAP	GRCh38.p7	3:47417762	CCTTCCCACCATCTG[A/G]AAGTCGTTCCCAGCT	22937
rs768013421	snp	A/G	4.95724e-05	0.00497833	synonymous-codon	SCAP	GRCh38.p7	3:47418441	ACCCAGCTGCCCGTA[A/G]TTGCGCGGGCATAGC	22937
rs768030053	snp	G/T			intron-variant	SCAP	GRCh38.p7	3:47464378	GGGACTGATTTGTGT[G/T]TTTTTTTTTAAAGTA	22937
rs768039091	snp	A/T	1.73447e-05	0.00294483	intron-variant	SCAP	GRCh38.p7	3:47435152	GCTGGGATGTACAAA[A/T]AGGAGATAAGAATTA	22937
rs768049986	snp	A/G	3.462e-05	0.00416039	intron-variant	SCAP	GRCh38.p7	3:47415095	CACCCCAGGCCCTCC[A/G]ACCTCTAAACTGCAG	22937
rs768117933	snp	A/T			intron-variant	SCAP	GRCh38.p7	3:47451852	CTCAGGGCTCTGCAC[A/T]ACCCACCCCGGTCCT	22937
rs768183336	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47465993	CAAAAATTAGCTGGG[C/T]GTGGTGGCAGGTGCC	22937
rs768225701	snp	C/T	0.000108478	0.0073639	intron-variant	SCAP	GRCh38.p7	3:47418528	CGCCGCCACCCTGCA[C/T]GGGAGGGCGGACTGC	22937
rs768321435	snp	A/G	1.69097e-05	0.00290768	intron-variant	SCAP	GRCh38.p7	3:47428485	ACAGAATGGGATTCA[A/G]GGAGGCCAGGGTCCC	22937
rs768331758	in-del	-/C	1.65952e-05	0.00288051	intron-variant	SCAP	GRCh38.p7	3:47414139	CAGTCCTGAGTCCTT[-/C]CCTAAAATCCCAAGA	22937
rs768341337	in-del	-/C			intron-variant	SCAP	GRCh38.p7	3:47430079	GCATCAAGATGTATG[-/C]ACACACCACACACGC	22937
rs768382134	snp	C/T	0.000165945	0.00910741	synonymous-codon, intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47425998	TGCCATGAACCTACG[C/T]GTGGAGAAGTAGATG	22937
rs768409175	snp	A/G	1.66131e-05	0.00288206	intron-variant	SCAP	GRCh38.p7	3:47414666	ACCTGGGACAGGGAT[A/G]GGCCTCAGGTTCTGG	22937
rs768447765	snp	A/G	1.64776e-05	0.00287028	intron-variant, missense, utr-variant-5-prime	SCAP	GRCh38.p7	3:47428577	GGGACAAAGGTGAAC[A/G]AAATACATCTACTGC	22937
rs768460492	snp	A/T	1.73673e-05	0.00294675	stop-gained	SCAP	GRCh38.p7	3:47414829	AGACAATACTCACTC[A/T]CAGTGTGTGGTCTTG	22937
rs768470984	snp	C/T			intron-variant, upstream-variant-2KB	SCAP, LOC105377073	GRCh38.p7	3:47475297	CCACTCAGAAGTAAA[C/T]AGAAGCAACATTAGT	22937
rs768498714	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47421093	CCAGCCCAAGAGGAG[C/G]AGTACCCGGACTGCA	22937
rs768509102	snp	C/G	1.65537e-05	0.0028769	synonymous-codon, intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47426094	GAAGTGCACGTGGAC[C/G]AGGCTCTCCGCCCGA	22937
rs768509116	snp	A/G	1.8659e-05	0.00305436	intron-variant	SCAP	GRCh38.p7	3:47419736	GGTACTCAGTGGGAG[A/G]AATGGGCCCCAACCC	22937
rs768528532	snp	A/G	4.97863e-05	0.00498906	synonymous-codon	SCAP	GRCh38.p7	3:47414043	GACACAGCCCTGGCC[A/G]CCAGTCACCAGCAGG	22937
rs768531247	snp	A/G	9.45028e-05	0.00687331	missense	SCAP	GRCh38.p7	3:47417816	CCACGCCACTGTCCC[A/G]GCGCTGCCTGCTGGG	22937
rs768531782	snp	G/T			intron-variant	SCAP	GRCh38.p7	3:47434132	GCCTCTATTTCAGCC[G/T]CAGAGTCAAGTTCAT	22937
rs768559137	in-del	-/GGGGGTGAGAGGGGGCGGGGGACGGGGGTGAGAGGGGGCGT	0.000196754	0.00991656	intron-variant	SCAP	GRCh38.p7	3:47417868	GGGGGCACGGGGGAG[lengthTooLong]GGGAGTGAGAAGGGG	22937
rs768583561	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47447920	TGAGGCAGGAGAATC[A/G]CTTGAACCCAGGAGG	22937
rs768636607	snp	C/G	1.65151e-05	0.00287355	missense	SCAP	GRCh38.p7	3:47413958	GGATCTGGCGGGCAG[C/G]CTGGGCCTCACTGTT	22937
rs768681076	snp	A/C	0.000209077	0.0102223	intron-variant	SCAP	GRCh38.p7	3:47417259	AAAGGCCCACAATCC[A/C]CGGGGCGGACAGCCG	22937
rs768763943	in-del	-/AAAAC			intron-variant	SCAP	GRCh38.p7	3:47464987	ACAGTGAACAATCTA[-/AAAAC]AAAATTAGGAAAACA	22937
rs768810038	in-del	-/G	4.37857e-05	0.00467878	intron-variant	SCAP	GRCh38.p7	3:47420525	CGGCCCTCCAGAAGA[-/G]GGCAGGGCAGGGCAG	22937
rs768835545	snp	C/G	3.61115e-05	0.00424905	intron-variant	SCAP	GRCh38.p7	3:47425440	GTGCAAGGCTCTCTG[C/G]CCTGAGCCCACCCTG	22937
rs768840956	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47470426	CTATAGTGAGATGTG[C/G]GACTGGTAAAAAGGA	22937
rs768915690	snp	C/T	3.64824e-05	0.00427081	intron-variant	SCAP	GRCh38.p7	3:47415195	CCTGGAAGAGAAGAA[C/T]AGCTGCCAGGGGCCT	22937
rs768941711	snp	A/G	6.67434e-05	0.00577644	utr-variant-5-prime	SCAP	GRCh38.p7	3:47443039	GGAAAGTGACCATGG[A/G]TCACCCTGGCACACA	22937
rs768951244	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47448622	TTATTCTACCTTCAT[A/G]TTCACTGACTCTTCT	22937
rs768974394	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47473605	TGTCAGAGCCGGTAA[A/C]ACACTGGCAACCACC	22937
rs768982772	snp	A/G	2.3414e-05	0.00342147	missense	SCAP	GRCh38.p7	3:47418659	AGCAGCCTTACTTGT[A/G]CAGCGTGACGTCTCC	22937
rs769005686	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47430386	TAACAGGCATGTCGC[A/G]GAGCACCCCAAAACA	22937
rs769048677	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47441192	GCCGTGAGCCACCAC[A/G]CCCGGCCAGGTCTTT	22937
rs769064345	snp	C/T	3.30874e-05	0.00406726	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47427116	AAAGCCTCATGTCAC[C/T]CAGCAGACCAGTCAA	22937
rs769085823	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47457112	TTTCATGTAAGAGAA[C/G]AGAAGTCTCTGCTTA	22937
rs769122576	snp	C/T	1.69269e-05	0.00290915	missense	SCAP	GRCh38.p7	3:47418165	GCGTTAGGCAATCCC[C/T]GGTCTGCGCGTCCCA	22937
rs769171650	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47458026	GGCACGGTGGCTCAC[A/G]CCTGTAATCCCAGAA	22937
rs769173591	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47439775	ACTGCACCCAGGGGC[C/T]AGGCAGGAAGAACAG	22937
rs769186856	in-del	-/TTTTTTTTTT			intron-variant	SCAP	GRCh38.p7	3:47416616	TCACACCCCTAACGC[-/TTTTTTTTTT]TTTTTTTTTTTTTTT	22937
rs769201313	snp	A/G	1.70592e-05	0.0029205	missense	SCAP	GRCh38.p7	3:47414862	TCCCAGTCACCAAGC[A/G]CCCAGCAGCGGCTTT	22937
rs769243198	snp	A/C	0.00211163	0.0324246	intron-variant	SCAP	GRCh38.p7	3:47418630	CCCGCACTCTTTCCC[A/C]CCCCACCCCACCCAG	22937
rs769255146	snp	G/T	4.72311e-05	0.00485935	missense	SCAP	GRCh38.p7	3:47417585	CACAGACCGCCCGGT[G/T]CCGGGGCTCGGGCTG	22937
rs769258893	snp	A/G	0.000119908	0.00774206	synonymous-codon	SCAP	GRCh38.p7	3:47417376	CCAGATGGAACCCTC[A/G]GCACTGGGGGCCCAG	22937
rs769275341	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47457339	TTCCTGTGGAAGCAG[C/T]AGCCCTCTTCTCTGA	22937
rs769308756	snp	A/G	1.89762e-05	0.00308022	stop-gained	SCAP	GRCh38.p7	3:47417666	AGGTGAGGTCAGGCT[A/G]GTCCCCGAAGAGGGA	22937
rs769375384	snp	A/G	1.64893e-05	0.0028713	intron-variant, missense, utr-variant-5-prime	SCAP	GRCh38.p7	3:47428613	GGTTCTTGTGCCAGG[A/G]AAACACTGAGGACTT	22937
rs769408807	snp	C/G			intron-variant, splice-acceptor-variant	SCAP	GRCh38.p7	3:47428671	CGGGGCACCCACATA[C/G]TGCAGAAGAAATGAG	22937
rs769431346	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47460340	GGAACTGATAAATGT[C/T]CATATTAAAAGGAAA	22937
rs769465628	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47453814	CCACACCTTTGCAGT[C/T]AAGGCTCTCTCTTTA	22937
rs769476952	snp	A/G			intron-variant, upstream-variant-2KB	SCAP, LOC105377073	GRCh38.p7	3:47475673	CCGGCCCGCACGGCT[A/G]CTGGACAGCGCCATG	22937
rs769484575	snp	C/T	1.69519e-05	0.0029113	synonymous-codon	SCAP	GRCh38.p7	3:47414938	CAGGTGACAGGCCAC[C/T]GTGTCGCTGCTGCTG	22937
rs769498186	snp	C/G	3.57673e-05	0.00422875	intron-variant	SCAP	GRCh38.p7	3:47425452	CTGGCCTGAGCCCAC[C/G]CTGTGGCCCAGTGGA	22937
rs769504120	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47466621	GAAGTTGGACTCTTA[C/T]ACACAAAAATTAACT	22937
rs769512736	in-del	-/C	1.66034e-05	0.00288122	intron-variant	SCAP	GRCh38.p7	3:47414164	CAAGAATCCTATGAT[-/C]CCCCATCCCCTCTAC	22937
rs769513073	snp	A/C/G	5.01872e-05	0.00500914	missense	SCAP	GRCh38.p7	3:47420651	GAAGACGGCTGCAAC[A/C/G]TGATGGTGTGGGGTG	22937
rs769546548	snp	A/G	1.65682e-05	0.00287817	synonymous-codon, intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47425573	TGACCACGGCAGCCA[A/G]GGCCAGCCCCCACTT	22937
rs769566939	in-del	-/A			intron-variant	SCAP	GRCh38.p7	3:47466580	ACAAATGCTACTGGG[-/A]AAACTGGATAGTTAC	22937
rs769590795	snp	A/C/G			intron-variant	SCAP	GRCh38.p7	3:47452997	GCTACTTGGAAGCCT[A/C/G]AGTGGGAAGGACTGC	22937
rs769602019	in-del	-/GGGGGCCAGGAGGGCGGAGTGAGA	3.90992e-05	0.00442132	intron-variant	SCAP	GRCh38.p7	3:47417829	CCGGCGCTGCCTGCT[-/GGGGGCCAGGAGGGCGGAGTGAGA]GGGGGCACGGGGGAG	22937
rs769626879	in-del	-/TA			intron-variant	SCAP	GRCh38.p7	3:47472485	AATAATAATAATAAT[-/TA]AATGAAGCTGAAATA	22937
rs769677247	snp	C/G			upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47476787	CCCACCTGCCCAGCT[C/G]TGGCCCAACTAGAGA	22937
rs769687190	snp	C/T	3.33684e-05	0.00408449	synonymous-codon	SCAP	GRCh38.p7	3:47420701	CTGCCGCTCGTAGCG[C/T]GTTGGCTGTCCCACT	22937
rs769687752	snp	A/G	6.03846e-05	0.00549442	intron-variant	SCAP	GRCh38.p7	3:47418537	CCTGCACGGGAGGGC[A/G]GACTGCTGTGAGACA	22937
rs769753791	snp	A/C			upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47477364	GAGATCGAAACCATC[A/C]TGGCTAACACGGTGG	22937
rs769791731	snp	C/G	1.65996e-05	0.00288089	intron-variant	SCAP	GRCh38.p7	3:47414157	TAAAATCCCAAGAAT[C/G]CTATGATCCCCATCC	22937
rs769799066	in-del	-/GT			downstream-variant-500B	PTPN23, SCAP	GRCh38.p7	3:47413649	GAGGGTCCAGGCAGA[-/GT]GTGTGCACAAACAAT	22937
rs769804886	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47422319	CTTGCCAGGCAAAGA[C/G]GTCCCACCTCAGAAG	22937
rs769845814	snp	G/T	1.65723e-05	0.00287852	intron-variant	SCAP	GRCh38.p7	3:47421059	CATGGGGATGGGGGG[G/T]TGCCGTGACCTCACT	22937
rs769888068	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47443600	AGGTCTAGCGAGGTC[A/G]GCCCTCAACATAAAA	22937
rs769889198	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47432520	GCCTCTATCTGTCCC[C/T]CACATCATCCCACAC	22937
rs769929004	in-del	-/ACCTCTAGACAGGTGTGGACTGAAGGGGGCA	1.64787e-05	0.00287038	intron-variant, frameshift-variant, utr-variant-5-prime	SCAP	GRCh38.p7	3:47428561	CCAGTTGGAATGCCC[lengthTooLong]GGGACAAAGGTGAAC	22937
rs769942680	snp	A/G	1.64961e-05	0.00287189	utr-variant-5-prime, synonymous-codon	SCAP	GRCh38.p7	3:47435086	ATCCTTCACAGGGGT[A/G]GTGAATTCCACAGGT	22937
rs769957556	in-del	-/G			intron-variant	SCAP	GRCh38.p7	3:47455617	AAAAAAAAAAAAAAA[-/G]AAACCAAAAGAAATC	22937
rs770001989	snp	A/G			missense	SCAP	GRCh38.p7	3:47414591	TCAATGTACACGGTC[A/G]TGATGGCCCCTGAGT	22937
rs770012235	snp	G/T	1.72639e-05	0.00293796	synonymous-codon	SCAP	GRCh38.p7	3:47419597	GGGCATGGGAGCCAG[G/T]GCTCCCTCACCCAAT	22937
rs770021078	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47456854	ACAAGGTGCTAAATT[C/T]CCGCGTATATAAGCA	22937
rs770054566	snp	C/T	4.95078e-05	0.00497508	synonymous-codon	SCAP	GRCh38.p7	3:47419477	ACCTCCACGCTCAGG[C/T]GACTCGCCTGGCGAC	22937
rs770055932	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47433438	TTCTATCATCATCCC[A/G]TCATTCAAAGAGCTC	22937
rs770058714	snp	A/G	4.49236e-05	0.00473918	missense	SCAP	GRCh38.p7	3:47418739	GCAGGTATGGGCCCC[A/G]GTGGGGGCCAGGCAC	22937
rs770098764	snp	C/T	1.64776e-05	0.00287028	intron-variant, missense, upstream-variant-2KB, utr-variant-5-prime	SCAP	GRCh38.p7	3:47427238	CTCACCCCGCTGTAC[C/T]TCCCAGGAACACCAA	22937
rs770127916	in-del	-/TCCACCATCCAGAGGCTGCTCGCACAGGAC	1.68789e-05	0.00290503	intron-variant	SCAP	GRCh38.p7	3:47420803	TGGTCAGGGCCTGAG[lengthTooLong]CGCTGTCCTGCCCGA	22937
rs770156152	snp	A/G	8.33924e-05	0.00645672	synonymous-codon	SCAP	GRCh38.p7	3:47418175	ATCCCCGGTCTGCGC[A/G]TCCCACACGCAGACG	22937
rs770175018	snp	A/G	0.000224653	0.010596	missense	SCAP	GRCh38.p7	3:47417588	AGACCGCCCGGTGCC[A/G]GGGCTCGGGCTGAGT	22937
rs770206358	snp	C/T	1.64743e-05	0.00287	intron-variant, missense, utr-variant-5-prime	SCAP	GRCh38.p7	3:47427578	AGCAGCAGGCATCCA[C/T]GCTCAGGGAGTAGGT	22937
rs770276197	snp	A/C	1.67111e-05	0.00289055	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47425621	TCTTCCCTGGAGGGC[A/C]GAGAGGGCGTATCAG	22937
rs770312738	snp	G/T			intron-variant	SCAP	GRCh38.p7	3:47442792	CATACAGAGGCCAAG[G/T]GCTCCATAGTGGTTA	22937
rs770327035	snp	A/G	1.66974e-05	0.00288936	missense	SCAP	GRCh38.p7	3:47414320	ACACATGGCTGACCC[A/G]GCTGCCAGTCAGTAC	22937
rs770360562	snp	C/G	1.64887e-05	0.00287125	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47427418	ATGGGCACCTTTACA[C/G]GTCTGAAGGGAACTT	22937
rs770437500	snp	A/G/T	0.000106423	0.00729394	intron-variant	SCAP	GRCh38.p7	3:47415044	AAGCAATGGGTAGAC[A/G/T]GCCCCTGCCCGTCCC	22937
rs770486234	snp	A/G			upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47477737	CAAGAAGGTAGGACT[A/G]CAGATGAGCGCCACC	22937
rs770554621	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47454058	CTGATAAAATTCAAC[C/T]CTCATCCTTTTAAGA	22937
rs770589028	snp	A/G	6.40759e-05	0.00565984	intron-variant	SCAP	GRCh38.p7	3:47418547	AGGGCGGACTGCTGT[A/G]AGACACACCTCACAG	22937
rs770594328	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47439989	CCTGATGGAGACAGG[A/C]ACATTCCCAAGCTGT	22937
rs770608563	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47439167	TAATCCCAGGACTTT[C/G]GGAGGCTGAAGTGGG	22937
rs770622802	snp	A/G	1.74805e-05	0.00295634	missense	SCAP	GRCh38.p7	3:47419614	CTCCCTCACCCAATG[A/G]GCTCTGTTCCGTCAC	22937
rs770661699	in-del	-/T			intron-variant	SCAP	GRCh38.p7	3:47416254	CCCAGGTTCACCAGC[-/T]TGGAGGTGGGGCCAG	22937
rs770668697	snp	G/T			intron-variant	SCAP	GRCh38.p7	3:47448867	TGTCTTTTCCCCTTA[G/T]GATTTTCCTGATTTT	22937
rs770671912	snp	A/G	1.8562e-05	0.00304642	intron-variant	SCAP	GRCh38.p7	3:47419718	GCCTGCAGTGGGGCA[A/G]GGGGTACTCAGTGGG	22937
rs770674034	snp	A/G	1.75029e-05	0.00295823	intron-variant	SCAP	GRCh38.p7	3:47418279	TGTTGGTATGGGCCA[A/G]GCTCCGGCCCTCCCC	22937
rs770716348	snp	A/G	1.65468e-05	0.00287631	intron-variant	SCAP	GRCh38.p7	3:47420880	CCCAGGACTCCCTCA[A/G]TACAGCCAGGGCTGA	22937
rs770769434	snp	A/C	0.000123544	0.00785856	intron-variant	SCAP	GRCh38.p7	3:47418638	CTTTCCCACCCCACC[A/C]CACCCAGCAGCCTTA	22937
rs770784740	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47461126	CTTTCATCCTGCTCA[C/T]CGCTGGCCCTAAGAC	22937
rs770793348	snp	A/C	1.65345e-05	0.00287524	intron-variant, utr-variant-5-prime	SCAP	GRCh38.p7	3:47434960	CCTGCCTCAGCCAGT[A/C]TCCACCCAACGCTCT	22937
rs770795938	snp	A/C	3.29973e-05	0.00406172	intron-variant, missense, utr-variant-5-prime	SCAP	GRCh38.p7	3:47428631	ACACTGAGGACTTCA[A/C]AAATATCTGCTGGAC	22937
rs770868179	snp	C/T	1.66721e-05	0.00288717	missense	SCAP	GRCh38.p7	3:47414293	GGGAGGTGACATCCC[C/T]ACGGTGAGCAAACAC	22937
rs770874815	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47462838	TCATGTCCCTACTGA[C/T]GTCCTAGAAGGTTGT	22937
rs770899316	snp	C/T	1.8449e-05	0.00303713	missense	SCAP	GRCh38.p7	3:47417710	CCCCGGGGGCGGTGT[C/T]TCAGGGGAGGGCTGT	22937
rs770920786	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47447799	ATCTCCTGAGGTCAG[C/G]AGTTCAAGACCAGCC	22937
rs770926191	snp	G/T	1.79867e-05	0.00299884	intron-variant	SCAP	GRCh38.p7	3:47419285	AAGGGGATGGTGAGT[G/T]GACACCATCGAGTGA	22937
rs770968108	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47424485	CCTGAAGGCCCACTC[A/G]CCTTTGTTGAGAAGC	22937
rs771000596	snp	A/G	2.36807e-05	0.0034409	synonymous-codon	SCAP	GRCh38.p7	3:47418819	GCGGAGCGTGACTGG[A/G]ATGACGGGCAGCAGG	22937
rs771036489	snp	A/G			missense	SCAP	GRCh38.p7	3:47419595	ACGGGCATGGGAGCC[A/G]GGGCTCCCTCACCCA	22937
rs771039662	snp	A/G			intron-variant, upstream-variant-2KB	SCAP, LOC105377073	GRCh38.p7	3:47475344	TAAGCAATACGGAAA[A/G]CTAGAAACCAAGCAA	22937
rs771049422	snp	A/C	1.90442e-05	0.00308573	missense	SCAP	GRCh38.p7	3:47417820	GCCACTGTCCCGGCG[A/C]TGCCTGCTGGGGGCC	22937
rs771051207	snp	A/G	0.000785237	0.019799	intron-variant	SCAP	GRCh38.p7	3:47417861	AGTGAGAGGGGGCAC[A/G]GGGGAGGGGGGTGAG	22937
rs771100180	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47469657	AGCCACTGCACCCAG[A/C]CACCAAATAATTTTA	22937
rs771115303	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47459027	TCAGGCTGGTTTCAA[A/G]CTCCTGACCTCAGGT	22937
rs771118180	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47435296	AAGCTGAAACTCAGA[A/C]GTCATCTAGATTAGA	22937
rs771175447	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47466808	AAAAACTTTTGGCCG[A/G]GCGTGGTGGCTCACG	22937
rs771178909	snp	A/C	1.6495e-05	0.0028718	utr-variant-5-prime, missense	SCAP	GRCh38.p7	3:47442882	CATACCAGCAGGCTA[A/C]GATGCAGAACCCTGT	22937
rs771185274	snp	C/T			downstream-variant-500B	PTPN23, SCAP	GRCh38.p7	3:47413481	CAGCTCCAGTAGCAC[C/T]GCCAGGAACTTAACT	22937
rs771288044	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47444921	GGATTACAGGTGCCC[A/G]CCACCACACCTGGCT	22937
rs771297313	snp	A/G	1.65853e-05	0.00287964	utr-variant-5-prime	SCAP	GRCh38.p7	3:47443002	GGGTCATCCTCAGCC[A/G]AAGTCACCTTGCTGC	22937
rs771341385	snp	C/T	1.65952e-05	0.00288051	intron-variant	SCAP	GRCh38.p7	3:47414554	CTGTACCCCCTACCC[C/T]ACCTGCAGGCCGCTT	22937
rs771343374	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47428814	CAAGTTCTTGAGTTT[C/G]CAGGATGGCAGATAA	22937
rs771350752	snp	A/G	1.70945e-05	0.00292351	intron-variant	SCAP	GRCh38.p7	3:47422391	CTGCACAGCTGGGGA[A/G]CACAGCAGTTGCTTC	22937
rs771360107	in-del	-/AA	1.6507e-05	0.00287284	intron-variant	SCAP	GRCh38.p7	3:47442862	TATCCAAGGCAACCC[-/AA]AAACATACCAGCAGG	22937
rs771404299	snp	C/T	1.66145e-05	0.00288218	missense, utr-variant-5-prime	SCAP	GRCh38.p7	3:47422525	TGATGGACCAGCTCT[C/T]GCTGCTTAGGCCTGC	22937
rs771417160	snp	A/C/T	3.37353e-05	0.00410689	intron-variant, missense, utr-variant-5-prime	SCAP	GRCh38.p7	3:47427644	ACTTGCAGACACAAC[A/C/T]CCTCCAAGCTCCTGA	22937
rs771419125	snp	A/G	1.86048e-05	0.00304993	intron-variant	SCAP	GRCh38.p7	3:47419729	GGCAGGGGGTACTCA[A/G]TGGGAGGAATGGGCC	22937
rs771543659	snp	A/T			intron-variant	SCAP	GRCh38.p7	3:47462949	TCTCAGCCTGACTCC[A/T]GGCTCCAATTCTCAT	22937
rs771568085	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47434290	CAGCACGAATCCAGG[C/G]ACCACAGAACAACAC	22937
rs771588257	snp	C/T	1.65165e-05	0.00287367	downstream-variant-500B, missense	PTPN23, SCAP	GRCh38.p7	3:47413930	CAGACAATGGCAGCG[C/T]TGTCCAGCACCAGGA	22937
rs771646275	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47430335	GAGCTTAACAGGGAT[A/G]TAAATGACAAGAGTG	22937
rs771654154	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47440862	CGAGACCCTGTCTCA[A/C]GGAAGAAAAAAAAGA	22937
rs771699463	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47439266	ATACAAAAAATAGCC[A/G]GACGTGGTGGCTCAC	22937
rs771707727	snp	C/G			upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47477963	GGAACTTACCTACAC[C/G]CCTTACCTATCCTGA	22937
rs771728213	snp	C/T	6.69949e-05	0.00578731	missense	SCAP	GRCh38.p7	3:47418416	CGCGCCTCCGCCGCC[C/T]GGGCCCACCACCCAG	22937
rs771765479	snp	A/C			intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47425694	AGTAGGTTGCCCTGA[A/C]AGTCGAGGAAGGGAA	22937
rs771769586	snp	G/T	9.0551e-05	0.0067281	synonymous-codon	SCAP	GRCh38.p7	3:47418366	GATCTCCGTCTCGGG[G/T]GGCGCATAGCCGTAG	22937
rs771778990	snp	A/G	1.64751e-05	0.00287007	intron-variant, synonymous-codon, utr-variant-5-prime	SCAP	GRCh38.p7	3:47427586	GCATCCATGCTCAGG[A/G]AGTAGGTTCCTGAGC	22937
rs771796506	snp	C/T	4.95479e-05	0.0049771	intron-variant, utr-variant-5-prime	SCAP	GRCh38.p7	3:47434970	CCAGTCTCCACCCAA[C/T]GCTCTGTGCTGGCCT	22937
rs771824668	snp	A/G	6.93782e-05	0.00588934	synonymous-codon	SCAP	GRCh38.p7	3:47417418	GGAGCCTTTCTCGGG[A/G]GAGCCACCCTCGTCC	22937
rs771853381	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47424568	GCCCACTGTCCCACA[A/C]TCCCCGCAGCAAACC	22937
rs771903635	snp	A/G	0.000183884	0.00958689	missense	SCAP	GRCh38.p7	3:47417716	GGGCGGTGTCTCAGG[A/G]GAGGGCTGTCCCCAG	22937
rs771919218	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47433977	AAAGCCACAAAACTG[A/G]TTTCACCACAAAACT	22937
rs771933318	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47449563	AGAGAAAAGGAGAAA[A/C]GACAAAGCAAACAAC	22937
rs771942359	snp	A/G	1.70866e-05	0.00292284	synonymous-codon	SCAP	GRCh38.p7	3:47415156	GAAGAAATCAAGGGA[A/G]CCGTTGAGCCGTGCA	22937
rs771983388	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47464352	GAGGGTCTCACTATG[C/T]TGCCCAGGCTGGGAC	22937
rs771985529	snp	C/T	0.00019784	0.00994389	utr-variant-5-prime, missense	SCAP	GRCh38.p7	3:47435075	GGGGGCGAGTAATCC[C/T]TCACAGGGGTGGTGA	22937
rs771987817	snp	C/T			utr-variant-3-prime, downstream-variant-500B	PTPN23, SCAP	GRCh38.p7	3:47413228	CTACATCATCATCAT[C/T]TCATGCCCACCTGCC	22937
rs772007263	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47432704	TTTTTTAGAGACAAG[A/G]TCTCACTCTATTGCC	22937
rs772028780	snp	C/T	0.000122825	0.00783566	intron-variant	SCAP	GRCh38.p7	3:47415054	TAGACGGCCCCTGCC[C/T]GTCCCACCAAGTGTG	22937
rs772037598	snp	A/C	1.69476e-05	0.00291093	intron-variant, utr-variant-3-prime, downstream-variant-500B	PTPN23, SCAP	GRCh38.p7	3:47413840	CCTCCTGCCTGGGCA[A/C]GGAGGCCCTGCGCTC	22937
rs772099957	in-del	-/AAG			intron-variant	SCAP	GRCh38.p7	3:47466461	ACCTGAAAAAAAGAA[-/AAG]AAGAAGAAAAAAGAA	22937
rs772137089	snp	A/G	0.000551116	0.0165908	intron-variant	SCAP	GRCh38.p7	3:47417871	GGCACGGGGGAGGGG[A/G]GTGAGAGGGGGCGGG	22937
rs772167078	snp	C/T	6.7944e-05	0.00582816	intron-variant	SCAP	GRCh38.p7	3:47417237	GCTGTGAGCACCTGC[C/T]AGCCAGAAAGGCCCA	22937
rs772174740	in-del	-/TG	1.66037e-05	0.00288125	intron-variant	SCAP	GRCh38.p7	3:47414540	ATGGGCCACAGACTC[-/TG]TACCCCCTACCCCAC	22937
rs772250584	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47422174	AGGGAAGCAGGCAGG[C/G]AGGGGTAGGAAGACA	22937
rs772261359	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47428944	GCAGAATGAGCTTGC[C/T]GATGTCACAGCCTGA	22937
rs772289607	in-del	-/ACACACAC			intron-variant	SCAP	GRCh38.p7	3:47443236	TCAATCCCAAAATAC[-/ACACACAC]ACACACACACACACA	22937
rs772310104	in-del	-/CAAAG			intron-variant	SCAP	GRCh38.p7	3:47430641	ATTTTAATCAGTTGA[-/CAAAG]CAAAGCCCAGTGTCT	22937
rs772352627	snp	C/T	1.67024e-05	0.0028898	splice-acceptor-variant	SCAP	GRCh38.p7	3:47422537	TCTCGCTGCTTAGGC[C/T]TGCAGAGGGCAGCAA	22937
rs772407314	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47470215	CAGTCTTATTGCTGA[C/T]GCTGGCAAACCATCA	22937
rs772436109	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47430337	GCTTAACAGGGATGT[A/C]AATGACAAGAGTGTT	22937
rs772461126	snp	C/T	1.66054e-05	0.00288139	intron-variant	SCAP	GRCh38.p7	3:47414174	TATGATCCCCATCCC[C/T]TCTACCTGCTGAATG	22937
rs772480411	snp	A/G	4.95638e-05	0.0049779	synonymous-codon	SCAP	GRCh38.p7	3:47418830	CTGGGATGACGGGCA[A/G]CAGGCTGATGTACCT	22937
rs772495181	in-del	-/AGA			intron-variant	SCAP	GRCh38.p7	3:47424510	AGAAGCTGTGTGTGG[-/AGA]AGAACGACTGTTCCT	22937
rs772522252	snp	C/T	0.000156507	0.00884471	synonymous-codon	SCAP	GRCh38.p7	3:47417496	TGGTGTGCAGACGGC[C/T]GCCAGCCCCTCCTCC	22937
rs772531598	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47469304	GTGAGCAGAGACCAC[A/G]CCGTTGCATTCCAGC	22937
rs772533599	snp	A/G	1.79069e-05	0.00299218	intron-variant	SCAP	GRCh38.p7	3:47419301	GACACCATCGAGTGA[A/G]GTGGCACCTGGCACG	22937
rs772590324	in-del	-/GCGGCG			utr-variant-5-prime, intron-variant, upstream-variant-2KB	SCAP, LOC105377073	GRCh38.p7	3:47475823	AGCACCTCCCAAGCT[-/GCGGCG]GCGGCGGCGGCGGCG	22937
rs772639862	snp	C/T			intron-variant, upstream-variant-2KB	SCAP, LOC105377073	GRCh38.p7	3:47475707	ACGCACCCCCGAACC[C/T]AGCGGCCCCCATTCC	22937
rs772658776	snp	C/G/T	5.1009e-05	0.00504998	missense	SCAP	GRCh38.p7	3:47414943	GACAGGCCACTGTGT[C/G/T]GCTGCTGCTGTACAC	22937
rs772712801	snp	C/T	1.70409e-05	0.00291893	synonymous-codon	SCAP	GRCh38.p7	3:47414863	CCCAGTCACCAAGCG[C/T]CCAGCAGCGGCTTTC	22937
rs772734617	snp	C/G	1.6495e-05	0.0028718	utr-variant-5-prime, synonymous-codon	SCAP	GRCh38.p7	3:47442931	GGGATAGGATGCACA[C/G]AGGAGCCCATGGTTG	22937
rs772744421	snp	A/C	0.000101351	0.00711796	missense	SCAP	GRCh38.p7	3:47418178	CCCGGTCTGCGCGTC[A/C]CACACGCAGACGTGG	22937
rs772749730	snp	G/T			intron-variant	SCAP	GRCh38.p7	3:47435683	AAGCAACCGTGCCTG[G/T]CTAGTTTATACATTT	22937
rs772782563	snp	C/T			downstream-variant-500B	PTPN23, SCAP	GRCh38.p7	3:47413536	AGGATGGTACCAAAC[C/T]GCCACACTACCAGGA	22937
rs772820492	snp	A/G	1.74644e-05	0.00295497	intron-variant	SCAP	GRCh38.p7	3:47425466	CCCTGTGGCCCAGTG[A/G]AGCCTGCTAGGGACC	22937
rs772837566	snp	C/G/T			intron-variant	SCAP	GRCh38.p7	3:47434305	GACCACAGAACAACA[C/G/T]AGAAGAAAGGGCACT	22937
rs772873995	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47437707	TGATCATGCCACTGC[A/G]TTCCAGCCTAGGTGA	22937
rs772952003	snp	C/T	4.95135e-05	0.00497537	synonymous-codon	SCAP	GRCh38.p7	3:47419492	TGACTCGCCTGGCGA[C/T]GTCTGGTTCTCAGGT	22937
rs772958610	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47422327	GCAAAGAGGTCCCAC[C/T]TCAGAAGCAAGGATG	22937
rs772960649	snp	G/T	1.68071e-05	0.00289884	intron-variant	SCAP	GRCh38.p7	3:47428495	ATTCAGGGAGGCCAG[G/T]GTCCCTGAGAGGGGT	22937
rs772986145	snp	A/G	9.32097e-05	0.00682614	missense	SCAP	GRCh38.p7	3:47418448	TGCCCGTAGTTGCGC[A/G]GGCATAGCACGCGGT	22937
rs773002790	snp	A/G	3.4782e-05	0.00417011	synonymous-codon	SCAP	GRCh38.p7	3:47419606	AGCCAGGGCTCCCTC[A/G]CCCAATGGGCTCTGT	22937
rs773031188	snp	A/G	0.000262364	0.0114505	missense	SCAP	GRCh38.p7	3:47417522	CCTCCTGGTACACCC[A/G]CTGCACCAGGCAGCT	22937
rs773046872	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47461000	GGTGAGGGTCCAGGA[A/G]CCCCTAGAGCTCTCT	22937
rs773060989	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47459969	CCCACCAGGAATGCA[C/T]TCCTTTCCCAGGGTC	22937
rs773084832	snp	C/T	4.97352e-05	0.00498649	missense	SCAP	GRCh38.p7	3:47414074	TTGTCTGAGATGACA[C/T]CCAAGCTTGCACCAC	22937
rs773147729	in-del	-/AGT	1.66062e-05	0.00288146	cds-indel	SCAP	GRCh38.p7	3:47414191	CTACCTGCTGAATGG[-/AGT]AGAACTTGATGCCTG	22937
rs773148499	snp	G/T			intron-variant	SCAP	GRCh38.p7	3:47458142	AAAATACAAAAATTA[G/T]CAGGGCGTGGCCAGG	22937
rs773156068	snp	C/T	9.243e-05	0.00679753	missense	SCAP	GRCh38.p7	3:47417587	CAGACCGCCCGGTGC[C/T]GGGGCTCGGGCTGAG	22937
rs773156877	snp	C/G	0.000148526	0.00861632	missense	SCAP	GRCh38.p7	3:47419495	CTCGCCTGGCGACGT[C/G]TGGTTCTCAGGTAGC	22937
rs773161158	snp	A/C/G	4.53158e-05	0.00475985	synonymous-codon	SCAP	GRCh38.p7	3:47418750	CCCCGGTGGGGGCCA[A/C/G]GCACTGCGGCCGTCC	22937
rs773189475	snp	A/G	1.64789e-05	0.0028704	intron-variant, utr-variant-5-prime	SCAP	GRCh38.p7	3:47434996	GGCCTCAGGAACATG[A/G]CGAGTACCCACCCAC	22937
rs773219231	snp	C/T	6.64033e-05	0.0057617	intron-variant	SCAP	GRCh38.p7	3:47414544	GCCACAGACTCTGTA[C/T]CCCCTACCCCACCTG	22937
rs773262453	snp	A/G	1.64898e-05	0.00287135	intron-variant, missense, utr-variant-5-prime	SCAP	GRCh38.p7	3:47428615	TTCTTGTGCCAGGGA[A/G]ACACTGAGGACTTCA	22937
rs773285224	snp	A/T			upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47478511	ACAGTCTCATTCTGT[A/T]GTCCAGGCTGGAGTG	22937
rs773344685	snp	A/T	1.65422e-05	0.0028759	stop-gained, intron-variant	SCAP	GRCh38.p7	3:47423951	GGGCGATCCGCAGCT[A/T]CACCTCCAGGTCTAC	22937
rs773389011	snp	C/T	4.6449e-05	0.00481896	synonymous-codon	SCAP	GRCh38.p7	3:47418810	CGGGTTCAGGCGGAG[C/T]GTGACTGGGATGACG	22937
rs773390383	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47460229	CAGCTAACACAATAG[C/T]GGTCCTGAGGTGACG	22937
rs773408976	in-del	-/G			intron-variant	SCAP	GRCh38.p7	3:47443132	TAACAAAGAGTACTT[-/G]GCTCTGCACACTAGG	22937
rs773419270	snp	G/T	1.65416e-05	0.00287586	utr-variant-5-prime, synonymous-codon	SCAP	GRCh38.p7	3:47435104	GAATTCCACAGGTCC[G/T]GTTCCTGGCAAGGGG	22937
rs773445612	snp	C/T	8.83041e-05	0.00664411	intron-variant	SCAP	GRCh38.p7	3:47417265	CCACAATCCCCGGGG[C/T]GGACAGCCGCTCTGC	22937
rs773449278	in-del	-/TTCAT			intron-variant	SCAP	GRCh38.p7	3:47448724	ATTTCTGATTTTCTG[-/TTCAT]TTCATTTCAAGAGCA	22937
rs773465508	snp	C/T	1.8151e-05	0.0030125	missense	SCAP	GRCh38.p7	3:47417743	CCAGGCTCCTCTGGA[C/T]CAGCCTTCCCACCAT	22937
rs773476213	snp	G/T			intron-variant	SCAP	GRCh38.p7	3:47466676	AAGAAGAGCTAAAAC[G/T]GTAAAGCCCTTAGAA	22937
rs773485375	snp	A/G	1.65894e-05	0.00288	missense, intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47425999	GCCATGAACCTACGC[A/G]TGGAGAAGTAGATGT	22937
rs773548561	snp	G/T	1.64784e-05	0.00287035	intron-variant, missense, upstream-variant-2KB, utr-variant-5-prime	SCAP	GRCh38.p7	3:47427245	CGCTGTACTTCCCAG[G/T]AACACCAAATAACAA	22937
rs773565318	snp	A/G	0.00013224	0.00813035	intron-variant, synonymous-codon, utr-variant-5-prime	SCAP	GRCh38.p7	3:47427625	GCCTGGCAGCAGGTC[A/G]GTCACTTGCAGACAC	22937
rs773582115	in-del	-/GAA	6.7415e-05	0.00580542	intron-variant	SCAP	GRCh38.p7	3:47428715	GGCAGCTGAGCACAG[-/GAA]GAAGAAAGACGGTCC	22937
rs773608429	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47473859	GTAGTAAACTTTTTA[C/T]CCACCTAATGACAGT	22937
rs773611737	snp	C/G	1.72728e-05	0.00293872	intron-variant	SCAP	GRCh38.p7	3:47418268	CAGAAGCCCGGTGTT[C/G]GTATGGGCCAGGCTC	22937
rs773628886	in-del	-/ACACACACACACACAG			intron-variant	SCAP	GRCh38.p7	3:47435504	CACACACACACACAC[-/ACACACACACACACAG]ATAGATAGGCGCCTG	22937
rs773640251	in-del	-/AAA			intron-variant	SCAP	GRCh38.p7	3:47432315	CAAGACTCCGTCTTG[-/AAA]AAAAAAAAAAAAAAA	22937
rs773671555	snp	A/T	1.6483e-05	0.00287076	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47427432	AGGTCTGAAGGGAAC[A/T]TGTACTGGGGCTACC	22937
rs773690096	in-del	-/C	1.69876e-05	0.00291436	frameshift-variant	SCAP	GRCh38.p7	3:47418335	CATGAGGTGGCCGCG[-/C]CAGCACAAGCGGCAC	22937
rs773715828	snp	C/T			utr-variant-5-prime, synonymous-codon	SCAP	GRCh38.p7	3:47442937	GGATGCACAGAGGAG[C/T]CCATGGTTGTAGAAG	22937
rs773740826	snp	A/G	1.66991e-05	0.00288951	missense	SCAP	GRCh38.p7	3:47414328	CTGACCCGGCTGCCA[A/G]TCAGTACATCCCACA	22937
rs773741593	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47452214	AACTCCCTGTCTGTT[C/T]TTCAGGGTCTTTAAT	22937
rs773778300	in-del	-/AA	3.30049e-05	0.00406219	frameshift-variant	SCAP	GRCh38.p7	3:47421015	CAGCCCCACGACAGC[-/AA]AGAGACAGAACTCCT	22937
rs773794293	snp	G/T	1.80166e-05	0.00300133	utr-variant-3-prime, downstream-variant-500B	PTPN23, SCAP	GRCh38.p7	3:47413198	TGAACAGGTTTTGCC[G/T]ACCTGGTCCTTACAC	22937
rs773826905	in-del	-/A			intron-variant, upstream-variant-2KB	SCAP, LOC105377073	GRCh38.p7	3:47474809	TCCAAACAAACAAAC[-/A]AAAAAACAAGTCTTT	22937
rs773868505	in-del	-/G			intron-variant	SCAP	GRCh38.p7	3:47472847	GCACTTTGGGAGGCC[-/G]AGGCGGGCGGATCAC	22937
rs773872046	snp	C/T	0.000130987	0.00809175	missense	SCAP	GRCh38.p7	3:47418671	TGTACAGCGTGACGT[C/T]TCCATGGGCCTGCAC	22937
rs773879735	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47461262	TCACATCTACATGGT[A/G]CTCATTCCCAAATAT	22937
rs773901227	snp	A/G	2.44723e-05	0.00349794	synonymous-codon	SCAP	GRCh38.p7	3:47417364	CAGCTCCAAGCTCCA[A/G]ATGGAACCCTCGGCA	22937
rs773942201	snp	C/T			upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47476901	TCCCCTCAGCCCCTG[C/T]CTACTGCCCGAGACA	22937
rs773966055	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47422580	CAACACATGGCCACT[C/G]TGCGACATGACTCAC	22937
rs773979797	snp	A/T			intron-variant	SCAP	GRCh38.p7	3:47466324	CTGGCATAAGGTCAG[A/T]CATATAAAACAATAG	22937
rs773991089	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47430557	ACCAAGGAAACCTGT[A/C]AGGGGATAACAGAAA	22937
rs773999691	snp	A/C	0.000277902	0.0117845	intron-variant	SCAP	GRCh38.p7	3:47418640	TTCCCACCCCACCCC[A/C]CCCAGCAGCCTTACT	22937
rs774018672	snp	A/T			intron-variant	SCAP	GRCh38.p7	3:47424539	TCCTACACAAAGCTC[A/T]ACCAGCTATCTGAGC	22937
rs774051545	snp	C/T	3.5049e-05	0.00418608	intron-variant	SCAP	GRCh38.p7	3:47418284	GTATGGGCCAGGCTC[C/T]GGCCCTCCCCTACCC	22937
rs774067106	snp	A/G	1.87728e-05	0.00306367	synonymous-codon	SCAP	GRCh38.p7	3:47417673	GTCAGGCTGGTCCCC[A/G]AAGAGGGAAGGCGGC	22937
rs774112057	snp	A/C	1.72291e-05	0.002935	intron-variant	SCAP	GRCh38.p7	3:47425473	GCCCAGTGGAGCCTG[A/C]TAGGGACCTACCCGC	22937
rs774122815	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47449136	GCAGAACTACTTGAG[C/G]AGTAATGTACTCCAC	22937
rs774130858	snp	C/G	1.66726e-05	0.00288722	synonymous-codon	SCAP	GRCh38.p7	3:47417595	CCGGTGCCGGGGCTC[C/G]GGCTGAGTGGGCTGT	22937
rs774131718	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47444817	GATGGGGTTGCCCAG[A/G]CTGGAGTGCAGTGGC	22937
rs774174292	snp	A/C/T	9.36724e-05	0.00684306	missense, stop-gained	SCAP	GRCh38.p7	3:47418362	GCACGATCTCCGTCT[A/C/T]GGGTGGCGCATAGCC	22937
rs774229333	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47432577	AACTCAGCAGTGAGT[C/T]GAGTAGGGAAGGAAG	22937
rs774285405	snp	G/T			intron-variant	SCAP	GRCh38.p7	3:47443448	GCTCTCTGTCAAACA[G/T]GCATTCTTCCCCCCC	22937
rs774293567	snp	A/G	3.92234e-05	0.00442833	intron-variant	SCAP	GRCh38.p7	3:47417829	CCGGCGCTGCCTGCT[A/G]GGGGCCAGGAGGGCG	22937
rs774303116	snp	C/T	1.65288e-05	0.00287474	intron-variant, utr-variant-5-prime	SCAP	GRCh38.p7	3:47434963	GCCTCAGCCAGTCTC[C/T]ACCCAACGCTCTGTG	22937
rs774306551	snp	C/T	1.71625e-05	0.00292933	synonymous-codon	SCAP	GRCh38.p7	3:47414956	GTCGCTGCTGCTGTA[C/T]ACTGGAGAGGCAGGG	22937
rs774314892	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47462883	CTTCCTGCTTCCCCA[C/T]AGGCTTTGTTCCTGG	22937
rs774442652	snp	A/G	3.30186e-05	0.00406303	missense	SCAP	GRCh38.p7	3:47419506	ACGTCTGGTTCTCAG[A/G]TAGCTTAGGGGCATC	22937
rs774496564	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47445037	TCAGCCTCCCAAAGT[A/G]CTGGGATTACAGGCA	22937
rs774515832	snp	C/T	1.67421e-05	0.00289323	synonymous-codon	SCAP	GRCh38.p7	3:47414354	CCACAGGCAGATGGC[C/T]CCATCTTGTCCTCCA	22937
rs774527295	snp	A/G	0.0001069	0.00731018	intron-variant	SCAP	GRCh38.p7	3:47417862	GTGAGAGGGGGCACG[A/G]GGGAGGGGGGTGAGA	22937
rs774530661	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47420235	GCCGATGAACCCGAC[C/T]CAGGGCAATGTGGTG	22937
rs774647190	in-del	-/A			intron-variant	SCAP	GRCh38.p7	3:47420287	GAGCACTCAACTAAC[-/A]GGCTCCTGTCCTGGG	22937
rs774665852	snp	A/C	1.70845e-05	0.00292267	intron-variant	SCAP	GRCh38.p7	3:47422393	GCACAGCTGGGGAGC[A/C]CAGCAGTTGCTTCCA	22937
rs774745158	snp	C/T	1.65198e-05	0.00287395	missense	SCAP	GRCh38.p7	3:47413979	CCTCACTGTTCTTCC[C/T]CAGGTAGACTGTCTG	22937
rs774749281	snp	A/C/G	3.34539e-05	0.00408975	synonymous-codon	SCAP	GRCh38.p7	3:47417145	CAAGAACACCAGAGC[A/C/G]GTAATGCCTGAGGAG	22937
rs774762162	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47453189	TTTTGCTACCTGCAT[C/T]TGCACTTCACTTCTG	22937
rs774773329	in-del	-/AGA			intron-variant	SCAP	GRCh38.p7	3:47436173	TACCTTTAAAAATCC[-/AGA]AGAAGGATTCCAATT	22937
rs774800441	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47454239	GGGCGAGGTGGCGGG[C/G]ACCTGTAGTCCCAGC	22937
rs774840099	snp	A/G	1.65952e-05	0.00288051	intron-variant	SCAP	GRCh38.p7	3:47414559	CCCCCTACCCCACCT[A/G]CAGGCCGCTTACCTG	22937
rs774862449	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47428825	GTTTGCAGGATGGCA[A/G]ATAAGAAAAGAAACA	22937
rs774892089	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47435775	ATTTTCAGGCTGGGC[A/G]CAGTGGGTTATGCCT	22937
rs774915990	snp	A/G	0.000197375	0.00993219	synonymous-codon	SCAP	GRCh38.p7	3:47418417	GCGCCTCCGCCGCCC[A/G]GGCCCACCACCCAGC	22937
rs774946355	in-del	-/ATG	1.65411e-05	0.00287581	cds-indel	SCAP	GRCh38.p7	3:47422509	GTGGCCATGTTCTTC[-/ATG]ATGGACCAGCTCTCG	22937
rs774947103	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47424669	GAAGGGAGGGCCCTG[C/T]GAAGGGTATGGCAGA	22937
rs774963308	snp	C/G	1.64849e-05	0.00287092	intron-variant, missense, utr-variant-5-prime	SCAP	GRCh38.p7	3:47427605	AGGTTCCTGAGCTTC[C/G]TAAGGCCTGGCAGCA	22937
rs774985661	snp	A/G			upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47478044	AGAAACCTTGGGCAT[A/G]AAGGAGTCCTCCTGA	22937
rs775060706	snp	A/G			intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47425706	TGACAGTCGAGGAAG[A/G]GAAAACTCCTGGTTT	22937
rs775068085	snp	A/G	1.66349e-05	0.00288395	utr-variant-5-prime, synonymous-codon	SCAP	GRCh38.p7	3:47435119	TGTTCCTGGCAAGGG[A/G]AGTTTCAGCAGTGGG	22937
rs775112572	snp	G/T			intron-variant	SCAP	GRCh38.p7	3:47418075	GAGATACGTGGCGGC[G/T]GGGGGTGGGGTGAGG	22937
rs775176341	snp	A/G	1.73872e-05	0.00294844	missense	SCAP	GRCh38.p7	3:47417419	GAGCCTTTCTCGGGG[A/G]AGCCACCCTCGTCCT	22937
rs775196436	snp	A/G	8.77124e-05	0.00662182	intron-variant	SCAP	GRCh38.p7	3:47415055	AGACGGCCCCTGCCC[A/G]TCCCACCAAGTGTGA	22937
rs775232580	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47421817	AGATGGCATCCTCCC[C/T]TTCCTGCAACTCCTT	22937
rs775233872	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47434016	CCAGCATCAGACCAT[A/G]CATCCTTTGACCTTC	22937
rs775244381	snp	A/G	6.59674e-05	0.00574277	utr-variant-5-prime, missense	SCAP	GRCh38.p7	3:47435082	AGTAATCCTTCACAG[A/G]GGTGGTGAATTCCAC	22937
rs775264147	snp	G/T			intron-variant	SCAP	GRCh38.p7	3:47444457	GCGTTAAGCGCACAT[G/T]CAAGTTTCCAATCCA	22937
rs775360696	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47473903	GGGGAAGGGCCCCAA[A/C]CCAGTGATTATAAAG	22937
rs775367542	snp	A/G	1.66877e-05	0.00288852	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47425987	CTCAGCCTCCCTGCC[A/G]TGAACCTACGCGTGG	22937
rs775377959	snp	A/G			synonymous-codon	SCAP	GRCh38.p7	3:47419678	GTCTGTGTATACCAG[A/G]ATGCCAATCCAGACA	22937
rs775418951	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47441014	TCAAGTGATTCTCCT[A/G]CCTCAGCCTCCCGAG	22937
rs775423834	snp	C/G/T	0.000100257	0.00707955	synonymous-codon, missense	SCAP	GRCh38.p7	3:47417163	AATGCCTGAGGAGAC[C/G/T]TCCTCGCTGCTGCAG	22937
rs775432962	snp	G/T	1.67913e-05	0.00289748	intron-variant, utr-variant-3-prime, downstream-variant-500B	PTPN23, SCAP	GRCh38.p7	3:47413849	TGGGCAAGGAGGCCC[G/T]GCGCTCAGTCCAGCT	22937
rs775457226	snp	A/T			intron-variant	SCAP	GRCh38.p7	3:47451703	CACCATGCCTGGCCC[A/T]CATAGACCCCTTCCT	22937
rs775479060	snp	C/T	1.64732e-05	0.0028699	intron-variant	SCAP	GRCh38.p7	3:47414107	CCCAGGTCCTGGAGG[C/T]AAGGACATGACAAGC	22937
rs775495421	in-del	-/CA	0.000454378	0.0150659	intron-variant	SCAP	GRCh38.p7	3:47417858	CGGAGTGAGAGGGGG[-/CA]CGGGGGAGGGGGGTG	22937
rs775611196	in-del	-/T	1.65971e-05	0.00288067	intron-variant	SCAP	GRCh38.p7	3:47414549	AGACTCTGTACCCCC[-/T]ACCCCACCTGCAGGC	22937
rs775686586	snp	C/G	1.72308e-05	0.00293515	intron-variant	SCAP	GRCh38.p7	3:47417249	TGCCAGCCAGAAAGG[C/G]CCACAATCCCCGGGG	22937
rs775723913	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47439370	GCCATGATTGTGCCA[C/T]TGCACTCCAGCCTGG	22937
rs775782835	snp	C/T	1.69556e-05	0.00291162	intron-variant	SCAP	GRCh38.p7	3:47418553	GACTGCTGTGAGACA[C/T]ACCTCACAGCCTGTC	22937
rs775823404	snp	A/G	2.57496e-05	0.00358806	synonymous-codon	SCAP	GRCh38.p7	3:47418840	GGGCAGCAGGCTGAT[A/G]TACCTGGATTCGGAC	22937
rs775857389	snp	A/C/G	3.30722e-05	0.00406635	intron-variant	SCAP	GRCh38.p7	3:47420896	TACAGCCAGGGCTGA[A/C/G]GAGGCGGGCAGGGCA	22937
rs775862799	in-del	-/GT			intron-variant	SCAP	GRCh38.p7	3:47419136	GGCTGGCAGCCACCA[-/GT]GTGACTCCTCAGAGC	22937
rs775876475	snp	C/G	2.12123e-05	0.00325664	intron-variant	SCAP	GRCh38.p7	3:47417841	GCTGGGGGCCAGGAG[C/G]GCGGAGTGAGAGGGG	22937
rs775904584	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47445705	GCCTCCCTTGTAGCT[A/G]GGAGCACAGGTGCAC	22937
rs775918165	snp	A/G	1.66358e-05	0.00288402	utr-variant-5-prime	SCAP	GRCh38.p7	3:47443029	CTGCCATCCCGGAAA[A/G]TGACCATGGATCACC	22937
rs775929741	snp	C/T	1.78512e-05	0.00298752	intron-variant	SCAP	GRCh38.p7	3:47419308	TCGAGTGAGGTGGCA[C/T]CTGGCACGGCCCAGC	22937
rs775984854	snp	G/T	6.52805e-05	0.00571279	intron-variant	SCAP	GRCh38.p7	3:47417872	GCACGGGGGAGGGGG[G/T]TGAGAGGGGGCGGGG	22937
rs776021290	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47470219	CTTATTGCTGATGCT[A/G]GCAAACCATCATACA	22937
rs776070178	snp	C/G/T	3.2992e-05	0.00406142	utr-variant-5-prime, synonymous-codon	SCAP	GRCh38.p7	3:47442934	ATAGGATGCACAGAG[C/G/T]AGCCCATGGTTGTAG	22937
rs776105953	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47454824	TTTACATCTTTCTCA[A/C]TCTCAAAGCTAAAAT	22937
rs776108316	snp	A/G	4.99355e-05	0.00499652	synonymous-codon, intron-variant	SCAP	GRCh38.p7	3:47423937	CACTGCGTTACCTTG[A/G]GCGATCCGCAGCTTC	22937
rs776128734	in-del	-/A			intron-variant	SCAP	GRCh38.p7	3:47416439	GCGCACTCTGTAACT[-/A]AAAAATGCAACCAAG	22937
rs776165538	snp	C/T	0.000103173	0.00718162	synonymous-codon	SCAP	GRCh38.p7	3:47419339	TCACCTCTTGGCCAG[C/T]GTGATGTTGTAATAG	22937
rs776177810	snp	C/T	1.73414e-05	0.00294455	synonymous-codon	SCAP	GRCh38.p7	3:47414833	AATACTCACTCTCAG[C/T]GTGTGGTCTTGGCTC	22937
rs776185648	snp	A/C	1.69522e-05	0.00291132	intron-variant	SCAP	GRCh38.p7	3:47422565	CAACAGGGCACAGGG[A/C]AACACATGGCCACTC	22937
rs776191896	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47451889	CTTCACTTCGTGTCA[C/T]CTCTCCCTGTTCTGG	22937
rs776199950	snp	C/T	0.00014498	0.00851287	missense	SCAP	GRCh38.p7	3:47417509	GCCGCCAGCCCCTCC[C/T]CCTGGTACACCCGCT	22937
rs776211748	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47440188	CCAGGAACAATAAAA[A/G]GTAAGCAATTAAATG	22937
rs776231507	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47459320	ATTTCCTGCAAGAAG[C/T]GTGCTTTGCTGGAGG	22937
rs776236659	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47434259	TGGTTTTCCTCAACA[A/G]CAGATTCAGCAAGTC	22937
rs776260704	snp	A/G	8.4513e-05	0.00649995	intron-variant	SCAP	GRCh38.p7	3:47428486	CAGAATGGGATTCAG[A/G]GAGGCCAGGGTCCCT	22937
rs776328252	snp	C/G	3.32414e-05	0.00407671	intron-variant	SCAP	GRCh38.p7	3:47414674	CAGGGATGGGCCTCA[C/G]GTTCTGGTCTCTGGG	22937
rs776350999	snp	C/T	1.65157e-05	0.0028736	synonymous-codon	SCAP	GRCh38.p7	3:47413959	GATCTGGCGGGCAGG[C/T]TGGGCCTCACTGTTC	22937
rs776363104	snp	C/G	3.6014e-05	0.00424331	intron-variant	SCAP	GRCh38.p7	3:47425446	GGCTCTCTGGCCTGA[C/G]CCCACCCTGTGGCCC	22937
rs776385822	snp	C/T	8.42637e-05	0.00649036	missense	SCAP	GRCh38.p7	3:47418377	CGGGTGGCGCATAGC[C/T]GTAGTCGTCGCAGGG	22937
rs776502967	snp	G/T	1.67508e-05	0.00289398	missense	SCAP	GRCh38.p7	3:47420643	TTCGGAAGGAAGACG[G/T]CTGCAACGTGATGGT	22937
rs776503240	snp	C/T			intron-variant, upstream-variant-2KB	SCAP, LOC105377073	GRCh38.p7	3:47475346	AGCAATACGGAAAAC[C/T]AGAAACCAAGCAAAA	22937
rs776507479	snp	C/G	1.66078e-05	0.00288161	missense	SCAP	GRCh38.p7	3:47414201	AATGGAGTAGAACTT[C/G]ATGCCTGTGCTGCGG	22937
rs776519890	in-del	-/C			intron-variant	SCAP	GRCh38.p7	3:47466416	TGAGTCATTCTTGAA[-/C]CTTGTTATGATGTCA	22937
rs776522882	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47459937	CAGACACTCCCAGAG[C/T]GGCCATTTATAGACC	22937
rs776540758	in-del	-/CTCACAG	1.67158e-05	0.00289096	frameshift-variant	SCAP	GRCh38.p7	3:47420675	TGGGGTGTGGACGGC[-/CTCACAG]CCAGCTGCCGCTCGT	22937
rs776635364	snp	C/T	9.69932e-05	0.00696327	missense	SCAP	GRCh38.p7	3:47418445	AGCTGCCCGTAGTTG[C/T]GCGGGCATAGCACGC	22937
rs776695327	in-del	-/TG			intron-variant	SCAP	GRCh38.p7	3:47448357	GAGTCTTTCTGCATG[-/TG]TGTGTGTGTGTGTGG	22937
rs776721986	snp	A/T			intron-variant	SCAP	GRCh38.p7	3:47457143	TTTGTCTATAAATGC[A/T]CAAAACACCTGGGAA	22937
rs776778325	snp	C/T	1.65302e-05	0.00287486	intron-variant, missense, utr-variant-5-prime	SCAP	GRCh38.p7	3:47427624	GGCCTGGCAGCAGGT[C/T]GGTCACTTGCAGACA	22937
rs776814107	snp	C/G			downstream-variant-500B	PTPN23, SCAP	GRCh38.p7	3:47413590	TCTGGCTTGCTCATC[C/G]TCCCCGTGCCACACT	22937
rs776825257	snp	A/G	1.65321e-05	0.00287502	intron-variant	SCAP	GRCh38.p7	3:47420904	GGGCTGAGGAGGCGG[A/G]CAGGGCAGGGCTCAG	22937
rs776850192	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47432248	CTTGAACCCGGGAGG[C/T]GGAGGTTCCAGTGAG	22937
rs776910833	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47425052	GCATTTAAATGTTCT[A/G]ATCATGAAAAAAAAA	22937
rs776922328	snp	C/T	0.000149533	0.00864546	synonymous-codon	SCAP	GRCh38.p7	3:47417685	CCCGAAGAGGGAAGG[C/T]GGCGGAGGGCCCCGG	22937
rs776930792	in-del	-/G	0.000405597	0.014235	intron-variant	SCAP	GRCh38.p7	3:47417876	GGGGGAGGGGGGTGA[-/G]AGGGGGCGGGGGACG	22937
rs776936437	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47430387	AACAGGCATGTCGCG[C/G]AGCACCCCAAAACAT	22937
rs776946620	snp	A/G	2.30641e-05	0.00339581	missense	SCAP	GRCh38.p7	3:47418661	CAGCCTTACTTGTAC[A/G]GCGTGACGTCTCCAT	22937
rs776965010	in-del	-/CTCTCTCTC			intron-variant	SCAP	GRCh38.p7	3:47443299	TCTCTCTCTCTCTCT[-/CTCTCTCTC]TCTCCCTCCCCGCCC	22937
rs776974087	snp	A/T			intron-variant	SCAP	GRCh38.p7	3:47441299	ACATAATGAGACCCC[A/T]TCTCTACAAAAGACG	22937
rs776978126	snp	G/T	0.000307692	0.0123997	intron-variant	SCAP	GRCh38.p7	3:47418097	GGGGTGAGGGGGGTT[G/T]TGGGGGCACAAAGGA	22937
rs776988943	in-del	-/CTAGAGAC			upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47476795	CCAGCTCTGGCCCAA[-/CTAGAGAC]CTAGAGACGCTGCCC	22937
rs777022777	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47424724	ACAGTGTCAAGCTCA[A/G]GAAAGGGAGCAGGTA	22937
rs777050970	snp	C/T	0.000198013	0.00994824	missense	SCAP	GRCh38.p7	3:47419482	CACGCTCAGGTGACT[C/T]GCCTGGCGACGTCTG	22937
rs777077539	snp	C/T	3.34521e-05	0.00408961	utr-variant-5-prime	SCAP	GRCh38.p7	3:47443041	AAAGTGACCATGGAT[C/T]ACCCTGGCACACACT	22937
rs777111657	snp	A/C	1.65619e-05	0.00287762	intron-variant, utr-variant-5-prime	SCAP	GRCh38.p7	3:47434950	CTGGCAGACCCCTGC[A/C]TCAGCCAGTCTCCAC	22937
rs777130881	snp	A/C	1.6546e-05	0.00287624	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47427120	CCTCATGTCACCCAG[A/C]AGACCAGTCAAGAGC	22937
rs777159104	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47463372	TCGATAAATCTTTCT[A/C]AAGCACAAATCACTA	22937
rs777172042	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47458063	GAGGCTGAGGTGGGC[A/G]GATCACCTGAGGTCT	22937
rs777204979	snp	A/C/G	2.10577e-05	0.00324475	synonymous-codon	SCAP	GRCh38.p7	3:47418702	CCCACCTGGGCCCTT[A/C/G]GGTCCTGCTTCCCAG	22937
rs777219119	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47418623	CCCCCTCCCCGCACT[C/T]TTTCCCACCCCACCC	22937
rs777247992	snp	A/T			intron-variant	SCAP	GRCh38.p7	3:47414525	CAGGAGTCAGCAAAC[A/T]TGGGCCACAGACTCT	22937
rs777304971	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47415864	ATGATTGGAAGTGGG[C/T]GGACAAGGAGAGACC	22937
rs777337058	snp	C/T	1.6734e-05	0.00289253	synonymous-codon	SCAP	GRCh38.p7	3:47420725	TCCCACTGGCTTGGC[C/T]GAGGGCAGGCAGGCC	22937
rs777337873	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47430181	CTCACAACAGCCTGA[C/T]GAGAAGCAAGGAGAG	22937
rs777376898	snp	C/G	1.81302e-05	0.00301078	missense	SCAP	GRCh38.p7	3:47417775	TGAAAGTCGTTCCCA[C/G]CTCTCCTGAGCCTCA	22937
rs777413072	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47453924	ATGCTATTTCCTCCA[C/T]AAGCCTTCTCTAAAC	22937
rs777430804	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47462400	GCACACGCAGTGAAG[A/C]CTCCATTCTTTCAAT	22937
rs777431592	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47456800	AAAAAAAAAAGATAA[A/G]TAAGATCTGGAAAAA	22937
rs777432017	snp	A/G	1.64787e-05	0.00287038	utr-variant-5-prime, missense	SCAP	GRCh38.p7	3:47435058	GGTCAGAGTCCACAG[A/G]TGGGGGCGAGTAATC	22937
rs777452957	snp	C/G	1.77593e-05	0.00297982	intron-variant	SCAP	GRCh38.p7	3:47415041	AGAAAGCAATGGGTA[C/G]ACGGCCCCTGCCCGT	22937
rs777474568	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47425297	TAGCTAGATATGCTA[C/T]ATACAAACACAAGTA	22937
rs777477060	snp	A/G	1.65195e-05	0.00287393	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47427302	TGACACAGAAATGAC[A/G]GCTACTGCAGAGCCA	22937
rs777506993	in-del	-/GGAGTGAGAGGGGGCACGGGGGAGG	2.18279e-05	0.00330355	intron-variant	SCAP	GRCh38.p7	3:47417843	GGGGGCCAGGAGGGC[-/GGAGTGAGAGGGGGCACGGGGGAGG]GGAGTGAGAGGGGGC	22937
rs777514900	snp	C/T	1.6585e-05	0.00287962	missense, intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47425587	AGGGCCAGCCCCCAC[C/T]TGGACTTGACCATGT	22937
rs777569596	snp	C/T	1.72104e-05	0.00293341	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47425952	TGACATGGAAATGCC[C/T]GTTTAGCTTGGAGAA	22937
rs777597143	in-del	-/G	4.17397e-05	0.00456816	intron-variant	SCAP	GRCh38.p7	3:47418871	GTGGGCAGCCTCAGC[-/G]GGGGGGCCTCCCAGG	22937
rs777599467	snp	A/G	1.65277e-05	0.00287464	intron-variant	SCAP	GRCh38.p7	3:47421038	AGAACTCCTGGAATC[A/G]GAGCACATGGGGATG	22937
rs777602531	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47418881	CTCAGCGGGGGGCCT[C/T]CCAGGGCTTCCTCCT	22937
rs777603225	snp	C/G			utr-variant-3-prime, downstream-variant-500B	PTPN23, SCAP	GRCh38.p7	3:47413431	ATAAACCACCCTGTT[C/G]TGTGGCCCGTGTCTG	22937
rs777616283	snp	C/T	1.64762e-05	0.00287016	intron-variant, missense, upstream-variant-2KB	SCAP	GRCh38.p7	3:47427179	GGTAGTGCTGGAAGA[C/T]CAGGGTGATGGTGTA	22937
rs777645695	in-del	-/CA			intron-variant	SCAP	GRCh38.p7	3:47416012	TGGAGGGGAGGATGT[-/CA]CAGCCAAAGCCCATG	22937
rs777657627	snp	A/G	1.69097e-05	0.00290768	intron-variant	SCAP	GRCh38.p7	3:47417227	GAGTCCAGAGGCTGT[A/G]AGCACCTGCCAGCCA	22937
rs777658182	snp	A/C/T	0.000332085	0.0128816	intron-variant	SCAP	GRCh38.p7	3:47414526	AGGAGTCAGCAAACA[A/C/T]GGGCCACAGACTCTG	22937
rs777677743	snp	C/T	1.80491e-05	0.00300403	intron-variant	SCAP	GRCh38.p7	3:47417284	CAGCCGCTCTGCCCA[C/T]CTTTAGCCCCTCTGC	22937
rs777684147	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47440690	CCTGGGCAACATGGC[A/G]AAACCCCAGCTCTAC	22937
rs777703879	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47449524	TGTCTCCACCACTAC[A/G]CAATTACGTGGAGGG	22937
rs777715695	snp	C/T	1.66272e-05	0.00288328	intron-variant	SCAP	GRCh38.p7	3:47418633	GCACTCTTTCCCACC[C/T]CACCCCACCCAGCAG	22937
rs777780298	snp	C/T	1.66021e-05	0.0028811	intron-variant	SCAP	GRCh38.p7	3:47414158	AAAATCCCAAGAATC[C/T]TATGATCCCCATCCC	22937
rs777795926	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47433475	ACATCACACCCCTTA[C/G]GGCCTCATCATTAAA	22937
rs777808954	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47439129	AAATGCATGACTAGG[C/T]TGAGCAAGGTGGCTT	22937
rs777814770	in-del	-/TTTTTTTT			intron-variant	SCAP	GRCh38.p7	3:47416618	ACACCCCTAACGCTT[-/TTTTTTTT]TTTTTTTTTTTTTTT	22937
rs777819308	snp	C/T	1.6649e-05	0.00288518	missense	SCAP	GRCh38.p7	3:47414266	TGATGACACAGGAGG[C/T]GGTACAGGTAAGGGA	22937
rs777821770	snp	A/C/G	3.88178e-05	0.00440541	intron-variant	SCAP	GRCh38.p7	3:47427678	CAGAGCTGCACAGGA[A/C/G]ACAGGACAAGGCACC	22937
rs777888657	snp	A/G	7.20072e-05	0.00599987	intron-variant	SCAP	GRCh38.p7	3:47419278	TTGGGGAAAGGGGAT[A/G]GTGAGTTGACACCAT	22937
rs777899838	snp	A/G	1.66018e-05	0.00288108	missense	SCAP	GRCh38.p7	3:47414634	TGAAGAGGCAGCACG[A/G]GTCCTCCAGACGGAA	22937
rs777901518	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47435242	TAAATTCTGTCAGGA[C/T]TGTACAAATGTGCAA	22937
rs777901727	snp	A/G	4.95839e-05	0.0049789	synonymous-codon	SCAP	GRCh38.p7	3:47422502	CAGCTCCGTGGCCAT[A/G]TTCTTCATGATGGAC	22937
rs777918757	snp	C/G	1.6517e-05	0.00287372	intron-variant	SCAP	GRCh38.p7	3:47442845	AAGACACTGGCCCAC[C/G]ATATCCAAGGCAACC	22937
rs777926348	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47452526	CCCCTCTCTCTGAAT[C/G]AAATCATAAACAAGG	22937
rs777953785	snp	C/T	1.70793e-05	0.00292222	missense	SCAP	GRCh38.p7	3:47415116	TAAACTGCAGGGGGC[C/T]GAGGGCAGTGTGGGT	22937
rs777984970	snp	A/C			intron-variant, upstream-variant-2KB	SCAP, LOC105377073	GRCh38.p7	3:47474996	AATAAAAGAAACACA[A/C]GCAACGCTAACATTA	22937
rs778129437	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47428727	CAGGAAGAAGAAAGA[C/T]GGTCCAATTCAAGGG	22937
rs778152694	snp	C/T	1.71314e-05	0.00292667	intron-variant, utr-variant-3-prime, downstream-variant-500B	PTPN23, SCAP	GRCh38.p7	3:47413825	CACACAGCACCCCAG[C/T]CTCCTGCCTGGGCAA	22937
rs778175096	snp	G/T	7.31663e-05	0.00604796	missense	SCAP	GRCh38.p7	3:47417413	GAAGGGGAGCCTTTC[G/T]CGGGGGAGCCACCCT	22937
rs778215976	snp	C/G	1.81651e-05	0.00301368	missense	SCAP	GRCh38.p7	3:47417785	TCCCAGCTCTCCTGA[C/G]CCTCAAGCCCGCTGC	22937
rs778216233	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47447127	CAGTTGTCTGGACCA[C/G]GCACAGTGGCTCACG	22937
rs778262423	snp	A/G	3.29462e-05	0.00405857	intron-variant, missense, upstream-variant-2KB, utr-variant-5-prime	SCAP	GRCh38.p7	3:47427549	AGTCATTCTGCCAGA[A/G]GTTCCCAGGGGACAG	22937
rs778268038	snp	C/T	1.84076e-05	0.00303372	missense	SCAP	GRCh38.p7	3:47419695	TGCCAATCCAGACAA[C/T]GGTGCCAGCCTGCAG	22937
rs778283250	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47457888	CTCCAGCCTGGGCAA[C/T]GGAGCGAGACTCCGT	22937
rs778318950	snp	A/G	3.68128e-05	0.00429011	intron-variant	SCAP	GRCh38.p7	3:47420539	AGGGCAGGGCAGGGC[A/G]GGGGTGGCAGGTACC	22937
rs778389126	snp	C/T	1.81004e-05	0.0030083	intron-variant	SCAP	GRCh38.p7	3:47435175	AAGAATTAGACACTA[C/T]GAGAGGCAGTCCTCT	22937
rs778452156	in-del	-/G			intron-variant	SCAP	GRCh38.p7	3:47439481	TCACCATGAGCAGCA[-/G]CTTGTTGAATCAAAT	22937
rs778483475	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47471733	AGCCACTGGTTCCCA[A/G]ATGTTTTGATCATGA	22937
rs778505510	snp	C/T	1.65195e-05	0.00287393	downstream-variant-500B, missense	PTPN23, SCAP	GRCh38.p7	3:47413928	TGCAGACAATGGCAG[C/T]GTTGTCCAGCACCAG	22937
rs778510155	snp	C/T	5.00246e-05	0.00500098	missense	SCAP	GRCh38.p7	3:47414295	GAGGTGACATCCCCA[C/T]GGTGAGCAAACACAT	22937
rs778530317	in-del	-/GACACA	1.65026e-05	0.00287246	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47427288	AAACCAGCAGGTACT[-/GACACA]GAAATGACAGCTACT	22937
rs778586363	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47416079	ACTGGCAGAAATCAA[C/T]ATCACTAAGGGCAAG	22937
rs778613192	snp	A/G	1.85696e-05	0.00304704	intron-variant	SCAP	GRCh38.p7	3:47419719	CCTGCAGTGGGGCAG[A/G]GGGTACTCAGTGGGA	22937
rs778655767	snp	C/T	2.52388e-05	0.00355229	synonymous-codon	SCAP	GRCh38.p7	3:47420566	TACCATGATGAGGCG[C/T]TGTGCCAGGCGGGTG	22937
rs778680277	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47456823	TGGAAAAATACAACT[C/G]CAATTCATATCGCTG	22937
rs778689239	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47451554	AGGCGTGCACCACCA[C/T]ACCCAACGAAATGTT	22937
rs778689257	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47465537	TTTGGGAGGTCAAGT[A/G]GGGAGGACTGCTTGA	22937
rs778749312	snp	A/C/G	6.89906e-05	0.00587293			GRCh38.p7	3:47418796	TCCAGAGCCTCCCTC[A/C/G]GGTTCAGGCGGAGCG	22937
rs778821280	snp	A/G	8.61568e-05	0.00656285	synonymous-codon	SCAP	GRCh38.p7	3:47418717	GGGTCCTGCTTCCCA[A/G]TGCCCAGCAGGTATG	22937
rs778833633	snp	A/C	1.71664e-05	0.00292966	intron-variant	SCAP	GRCh38.p7	3:47414430	CACCATGGTGTAATA[A/C]CTCTGTCAACAGTGG	22937
rs778834368	snp	C/T	3.29641e-05	0.00405968	utr-variant-5-prime, synonymous-codon	SCAP	GRCh38.p7	3:47435065	GTCCACAGGTGGGGG[C/T]GAGTAATCCTTCACA	22937
rs778896582	snp	C/T	1.65021e-05	0.00287241	missense	SCAP	GRCh38.p7	3:47419464	CAACCTCTGCTGGAC[C/T]TCCACGCTCAGGTGA	22937
rs778903679	snp	G/T	0.000265252	0.0115133	stop-gained	SCAP	GRCh38.p7	3:47422466	GGGCACTAGGGTGAA[G/T]TAGCCGATGAGGATG	22937
rs778919276	in-del	-/AGGGC	0	0	intron-variant	SCAP	GRCh38.p7	3:47420523	CCGGCCCTCCAGAAG[-/AGGGC]AGGGCAGGGCAGGGC	22937
rs778923043	snp	A/G	1.67913e-05	0.00289748	synonymous-codon	SCAP	GRCh38.p7	3:47414908	TTTTTGGTGTGCACA[A/G]GGCACTGTGTGGGTC	22937
rs778925980	snp	A/G	1.65809e-05	0.00287926	synonymous-codon, intron-variant, utr-variant-5-prime	SCAP	GRCh38.p7	3:47425538	GAGTCCCACAGACAT[A/G]AGCAGCGAGCTGAGC	22937
rs778927789	snp	A/G	1.84245e-05	0.00303511	missense	SCAP	GRCh38.p7	3:47417713	CGGGGGCGGTGTCTC[A/G]GGGGAGGGCTGTCCC	22937
rs778949085	snp	A/G			missense, intron-variant	SCAP	GRCh38.p7	3:47424029	CAATAACCACCACAA[A/G]GTAGGGGAAAATCTC	22937
rs778951286	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47422052	GGAAGGGTCTAGGAA[C/T]CCCACGGTGCTTCTC	22937
rs778956451	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47442460	CTCTGAGGTTAGCCT[A/G]CCACAGGTTGTCCAA	22937
rs778990905	snp	A/G	5.23802e-05	0.00511736	intron-variant	SCAP	GRCh38.p7	3:47414791	CCCACCCCGTGCCGG[A/G]CCACTCCAGCACCCA	22937
rs779012795	snp	C/G	1.97666e-05	0.00314371	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47426199	GGGTGGGGGTAAATG[C/G]AAGTGTTGCTCTTGG	22937
rs779021315	snp	A/G	0.000107452	0.00732901	synonymous-codon	SCAP	GRCh38.p7	3:47418148	CCCTGGGCGCGGAAT[A/G]CGCGTTAGGCAATCC	22937
rs779040146	snp	C/T			upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47477277	TATAAAGAAAGTATT[C/T]GCTGGGCGCGGTGGC	22937
rs779126341	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47459816	TCAAGAGCAGAGAAC[C/T]GGTCTGACCTCAAAT	22937
rs779135884	snp	C/T	1.67211e-05	0.00289142	synonymous-codon	SCAP	GRCh38.p7	3:47420683	GGACGGCCTCACAGC[C/T]AGCTGCCGCTCGTAG	22937
rs779138307	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47430316	TCTGCCATCTACCTT[C/T]CAAGAGCTTAACAGG	22937
rs779194978	snp	C/G	1.65594e-05	0.0028774	synonymous-codon	SCAP	GRCh38.p7	3:47414025	GTTTAGGTCCCAAAA[C/G]GAGACACAGCCCTGG	22937
rs779234569	snp	A/G	1.66004e-05	0.00288096	utr-variant-5-prime	SCAP	GRCh38.p7	3:47443013	AGCCGAAGTCACCTT[A/G]CTGCCATCCCGGAAA	22937
rs779245102	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47428185	AGCTTGCTTCTCGTC[A/G]GCAGAGACACCACCA	22937
rs779296348	snp	A/G	0.000233027	0.0107916	utr-variant-5-prime	SCAP	GRCh38.p7	3:47443024	CCTTGCTGCCATCCC[A/G]GAAAGTGACCATGGA	22937
rs779316145	snp	A/G	1.66056e-05	0.00288141	missense	SCAP	GRCh38.p7	3:47414646	ACGAGTCCTCCAGAC[A/G]GAACACCTGGGACAG	22937
rs779318516	snp	A/C			upstream-variant-2KB, intron-variant, nc-transcript-variant	SCAP, LOC105377073	GRCh38.p7	3:47476669	GAGCTGGTATTGTAC[A/C]TGTCCTCGCATTTGG	22937
rs779359225	snp	C/T	1.70778e-05	0.00292209	missense	SCAP	GRCh38.p7	3:47418412	TCCCCGCGCCTCCGC[C/T]GCCCGGGCCCACCAC	22937
rs779367822	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47470164	AACAGGGGATCAAGA[A/G]CTAGCCTTAAGAGAA	22937
rs779372938	snp	C/T	1.6949e-05	0.00291105	intron-variant	SCAP	GRCh38.p7	3:47417115	GGCTGAGGCAGGCCA[C/T]GCTCACCTTTTGTCC	22937
rs779384233	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47431876	CTTTAGGATACATTA[C/G]TTAGAATTTTTTTGC	22937
rs779389331	in-del	-/C			intron-variant	SCAP	GRCh38.p7	3:47429209	ACCTTCAATATAAAG[-/C]TTTTCTTTTCCCCAA	22937
rs779430670	snp	C/T	1.72059e-05	0.00293303	missense	SCAP	GRCh38.p7	3:47420613	CAACACGCAGCCTCT[C/T]GGGGAGCCGCAGGTT	22937
rs779461666	snp	G/T			intron-variant	SCAP	GRCh38.p7	3:47464372	CAGGCTGGGACTGAT[G/T]TGTGTTTTTTTTTTT	22937
rs779479390	snp	A/G	1.64814e-05	0.00287061	intron-variant, synonymous-codon, utr-variant-5-prime	SCAP	GRCh38.p7	3:47428550	GGATCTCCTCCACCA[A/G]TTGGAATGCCCGGGA	22937
rs779479896	snp	A/G			intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47426987	CATCCCCATTAAAAT[A/G]TGGTAGACAGCATCA	22937
rs779562840	in-del	-/TCATC	1.86235e-05	0.00305146	utr-variant-3-prime, downstream-variant-500B	PTPN23, SCAP	GRCh38.p7	3:47413223	TACACTACATCATCA[-/TCATC]TCATCTCATGCCCAC	22937
rs779581415	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47447356	CAAGATCACGCCACT[C/G]CACTCCAGCCTAGGT	22937
rs779591203	snp	A/G	6.7914e-05	0.00582687	synonymous-codon	SCAP	GRCh38.p7	3:47417565	TGGGGAGTCCCGAGA[A/G]CGGCCACAGACCGCC	22937
rs779631744	snp	G/T			intron-variant	SCAP	GRCh38.p7	3:47458735	TACCTACATTCTTAC[G/T]CCCTCTTGACCTGGT	22937
rs779664032	snp	A/T	1.66815e-05	0.00288799	missense	SCAP	GRCh38.p7	3:47420693	ACAGCCAGCTGCCGC[A/T]CGTAGCGCGTTGGCT	22937
rs779666704	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47422810	AGGGAAGAAGCAGAG[C/T]GTGGAGATGAGAAAA	22937
rs779727821	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47453648	CCCTTAAACTAATAA[C/T]TACTTTTACTATTTC	22937
rs779731444	in-del	-/T			intron-variant	SCAP	GRCh38.p7	3:47436891	CACCAAAGGTAACTG[-/T]TTAGAATCTCTATCA	22937
rs779735698	snp	C/G	1.65946e-05	0.00288046	intron-variant	SCAP	GRCh38.p7	3:47414141	GTCCTGAGTCCTTCC[C/G]TAAAATCCCAAGAAT	22937
rs779757598	in-del	-/TAGCCCCTCTGCCCACCTC	1.81056e-05	0.00300873	intron-variant	SCAP	GRCh38.p7	3:47417287	CGCTCTGCCCACCTT[-/TAGCCCCTCTGCCCACCTC]TAGCCCCTCTGCCCA	22937
rs779768392	snp	C/G	1.65353e-05	0.00287531	intron-variant	SCAP	GRCh38.p7	3:47427718	TGCCACCACAGGGCA[C/G]ACCTGCTGTACTTAG	22937
rs779809130	in-del	-/AAT/AATAAT			intron-variant	SCAP	GRCh38.p7	3:47472463	AAAATAAAATAAAAT[-/AAT/AATAAT]AATAATAATAATAAT	22937
rs779887157	snp	G/T	4.21026e-05	0.00458798	intron-variant	SCAP	GRCh38.p7	3:47417855	GGGCGGAGTGAGAGG[G/T]GGCACGGGGGAGGGG	22937
rs779928496	snp	C/T	0.000115751	0.00760672	intron-variant	SCAP	GRCh38.p7	3:47442823	GGGTTAGAAAACCTA[C/T]TGTCCTAAGACACTG	22937
rs779981590	snp	C/G	1.65444e-05	0.00287609	synonymous-codon, intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47426091	CTTGAAGTGCACGTG[C/G]ACCAGGCTCTCCGCC	22937
rs780003352	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47428331	TGCATAGGTCCAAGC[A/G]GAATGCAGCCACCGT	22937
rs780005638	snp	A/G	0.000113246	0.00752397	utr-variant-3-prime, downstream-variant-500B	PTPN23, SCAP	GRCh38.p7	3:47413233	TCATCATCATCTCAT[A/G]CCCACCTGCCCACAC	22937
rs780035452	snp	A/C/T	8.05121e-05	0.00634425	intron-variant	SCAP	GRCh38.p7	3:47418888	GGGGGCCTCCCAGGG[A/C/T]TTCCTCCTGCTGTGC	22937
rs780072470	snp	C/T	5.13668e-05	0.00506762	missense	SCAP	GRCh38.p7	3:47415158	AGAAATCAAGGGAAC[C/T]GTTGAGCCGTGCAGC	22937
rs780097807	snp	A/G	1.7042e-05	0.00291903	missense	SCAP	GRCh38.p7	3:47418150	CTGGGCGCGGAATGC[A/G]CGTTAGGCAATCCCC	22937
rs780097900	snp	A/G	1.67058e-05	0.00289009	missense	SCAP	GRCh38.p7	3:47419551	AGAAGGCAGGGTCCG[A/G]GTGGCTGGGGGGCAG	22937
rs780150760	snp	C/T	7.55373e-05	0.00614515	missense	SCAP	GRCh38.p7	3:47418228	CCAGCAGCATGCCGT[C/T]GCTGGCCAGGCACTC	22937
rs780168122	snp	C/T	5.66364e-05	0.00532118	missense	SCAP	GRCh38.p7	3:47417311	CTGCCCACCTCCAGC[C/T]GGCCGCTGCTCCGCC	22937
rs780176042	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47462108	CTACTTCGTTTTGTG[A/G]TAAAAAAAAATTATT	22937
rs780186831	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47460746	TATTTTTAGTAGATA[C/T]GGGGTTTCACCATCC	22937
rs780213689	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47423761	CCCATGGCTCCCCAG[C/G]GCACACACTCAAGAG	22937
rs780251043	snp	A/C	1.64787e-05	0.00287038	intron-variant, missense, utr-variant-5-prime	SCAP	GRCh38.p7	3:47428565	GTTGGAATGCCCGGG[A/C]CAAAGGTGAACGAAA	22937
rs780277035	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47447549	CAAAATTGGCTGGGT[A/G]TGGTGGCGAGTGCCT	22937
rs780288481	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47419900	TTGCTGCTGGAGGGG[A/C]CTGCTTGCCTTTCCA	22937
rs780338953	in-del	-/TAA			intron-variant	SCAP	GRCh38.p7	3:47464787	CACTGCCTCATTTAC[-/TAA]CCTTTCTCTCCAGGC	22937
rs780373009	snp	C/T	1.64735e-05	0.00286993	intron-variant, missense, upstream-variant-2KB, utr-variant-5-prime	SCAP	GRCh38.p7	3:47427205	GTGTAGGAGACCATC[C/T]TCTTCCTGGTGTAGA	22937
rs780377772	snp	G/T	1.80504e-05	0.00300414	intron-variant	SCAP	GRCh38.p7	3:47424078	GAAGGTGAGGACAGT[G/T]TTGTGGTGGTTCCCA	22937
rs780386828	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47473202	TCAAATTCGCTAGGT[A/G]ACCCAGGGCCAGTCA	22937
rs780395702	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47460960	AAGCCAAGAGATGAG[A/G]CTCACCTGGGCCCCT	22937
rs780398634	in-del	-/AATAAT			intron-variant	SCAP	GRCh38.p7	3:47472130	ACTCCATCTCAAAAA[-/AATAAT]AATAATAATTAAATG	22937
rs780399274	snp	C/T			intron-variant, upstream-variant-2KB	SCAP, LOC105377073	GRCh38.p7	3:47474627	CAGCAAGACCCCCAT[C/T]TCTACAAAAAAATAC	22937
rs780497763	snp	A/G	5.82089e-05	0.00539454	synonymous-codon	SCAP	GRCh38.p7	3:47417574	CCGAGAGCGGCCACA[A/G]ACCGCCCGGTGCCGG	22937
rs780555007	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47433126	TAAGTCAGCCCTGCA[C/T]CTGGCTGAGTTATAT	22937
rs780557432	snp	A/C			intron-variant, missense, utr-variant-5-prime	SCAP	GRCh38.p7	3:47428546	TTCCGGATCTCCTCC[A/C]CCAGTTGGAATGCCC	22937
rs780610708	snp	C/T	9.00666e-05	0.00671008	utr-variant-3-prime, downstream-variant-500B	PTPN23, SCAP	GRCh38.p7	3:47413197	CTGAACAGGTTTTGC[C/T]TACCTGGTCCTTACA	22937
rs780615493	snp	A/G	1.65685e-05	0.00287819	synonymous-codon, intron-variant, utr-variant-5-prime	SCAP	GRCh38.p7	3:47425547	AGACATGAGCAGCGA[A/G]CTGAGCACTGTGACC	22937
rs780622489	snp	A/C	1.74665e-05	0.00295515	intron-variant	SCAP	GRCh38.p7	3:47414804	GGGCCACTCCAGCAC[A/C]CAAGAGACAAGACAA	22937
rs780642919	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47432086	TTGGGAGGCCGAGGC[A/G]GATGGATCAATCACA	22937
rs780665006	snp	A/C	1.68795e-05	0.00290507	intron-variant	SCAP	GRCh38.p7	3:47420792	TGGGGGCACAGTGGT[A/C]AGGGCCTGAGTCCAC	22937
rs780667235	snp	A/G	0.000541712	0.0164488	intron-variant	SCAP	GRCh38.p7	3:47418529	GCCGCCACCCTGCAC[A/G]GGAGGGCGGACTGCT	22937
rs780762321	snp	C/T	1.66363e-05	0.00288407	missense	SCAP	GRCh38.p7	3:47414254	CCAGGCCACTGCTGA[C/T]GACACAGGAGGTGGT	22937
rs780779658	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47444419	GAATGCCTATTGCTC[A/G]TTCTACCTTTCCGAA	22937
rs780815229	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47456580	AGACCAGTCTGACCA[A/G]TATGGCAAAACCCTG	22937
rs780834992	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47466443	GTCAGCACTACCCAT[C/T]TAACCTGAAAAAAAG	22937
rs780878382	snp	G/T			upstream-variant-2KB, intron-variant	SCAP, LOC105377073	GRCh38.p7	3:47477315	TGTAATCCCAGCACT[G/T]TGGGAGGCCAACACG	22937
rs780901074	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47439089	CCTGATAACGCTGTC[A/G]TAAATTGAAAATATC	22937
rs780901724	in-del	-/AGGGAAGGCGGC	1.87054e-05	0.00305816	cds-indel	SCAP	GRCh38.p7	3:47417676	GGCTGGTCCCCGAAG[-/AGGGAAGGCGGC]AGGGAAGGCGGCGGA	22937
rs780909102	in-del	-/ATG	1.6601e-05	0.00288101	intron-variant	SCAP	GRCh38.p7	3:47414160	AATCCCAAGAATCCT[-/ATG]ATCCCCATCCCCTCT	22937
rs780930197	snp	A/G	1.92077e-05	0.00309895	synonymous-codon	SCAP	GRCh38.p7	3:47417658	AATTAAGCAGGTGAG[A/G]TCAGGCTGGTCCCCG	22937
rs780993031	snp	A/G	1.64836e-05	0.0028708	intron-variant, synonymous-codon, upstream-variant-2KB	SCAP	GRCh38.p7	3:47427162	TCAATCTTACTTGGC[A/G]TGGTAGTGCTGGAAG	22937
rs781013998	snp	C/G	1.654e-05	0.00287571	utr-variant-5-prime, missense	SCAP	GRCh38.p7	3:47442976	TATCTTCTCACGCAG[C/G]CTTTCAGTCAGGGTC	22937
rs781014598	snp	A/C			intron-variant	SCAP	GRCh38.p7	3:47422227	GGCTAGGTGCTCAAT[A/C]TGGGAACCCAGCCAG	22937
rs781034412	in-del	-/ACC			intron-variant	SCAP	GRCh38.p7	3:47466133	GAGACTGTCTTAAAA[-/ACC]ACCAAAAAAAAAAAA	22937
rs781068305	snp	A/G	7.043e-05	0.0059338	intron-variant	SCAP	GRCh38.p7	3:47417859	GGAGTGAGAGGGGGC[A/G]CGGGGGAGGGGGGTG	22937
rs781112030	in-del	-/CTC			intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47425712	TCGAGGAAGGGAAAA[-/CTC]CTGGTTTCACCAAAG	22937
rs781138679	snp	A/G	3.49089e-05	0.00417771	utr-variant-5-prime, synonymous-codon, intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47426166	ACGCAGGCTGCCCAG[A/G]AACCTGGTCAAGGAG	22937
rs781191305	snp	C/T	1.67781e-05	0.00289634	synonymous-codon	SCAP	GRCh38.p7	3:47417130	CGCTCACCTTTTGTC[C/T]AAGAACACCAGAGCG	22937
rs781220425	snp	C/G			intron-variant	SCAP	GRCh38.p7	3:47448627	CTACCTTCATGTTCA[C/G]TGACTCTTCTGTCTT	22937
rs781246250	snp	A/G	3.36174e-05	0.0040997	intron-variant	SCAP	GRCh38.p7	3:47417212	GCGTCCCACACCTAC[A/G]AGTCCAGAGGCTGTG	22937
rs781339205	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47463981	GGACTACAGGCATGA[A/G]CCACCACATCTGGCT	22937
rs781360786	snp	G/T			intron-variant	SCAP	GRCh38.p7	3:47473627	GCAACCACCAATGGT[G/T]AGAGTAAGCAAACAG	22937
rs781363480	snp	A/G	1.66078e-05	0.00288161	intron-variant	SCAP	GRCh38.p7	3:47414529	AGTCAGCAAACATGG[A/G]CCACAGACTCTGTAC	22937
rs781391461	in-del	-/AG	1.64906e-05	0.00287142	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47427417	ATGGGCACCTTTACA[-/AG]GGTCTGAAGGGAACT	22937
rs781460321	snp	C/T	5.11775e-05	0.00505827	missense	SCAP	GRCh38.p7	3:47419581	GCATGCCACTAGGCA[C/T]GGGCATGGGAGCCAG	22937
rs781476668	snp	G/T	1.76733e-05	0.0029726	intron-variant	SCAP	GRCh38.p7	3:47415013	GGACAAAAGGCCAAG[G/T]GAAGAATCTCTGAGA	22937
rs781519926	snp	A/G/T	6.62903e-05	0.00575686	intron-variant	SCAP	GRCh38.p7	3:47421058	ACATGGGGATGGGGG[A/G/T]GTGCCGTGACCTCAC	22937
rs781531317	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47458889	CGGCTCACTGCAACC[C/T]CAGCCTCCTGGGTTC	22937
rs781547219	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47459562	ACATATGAGTAGGAC[C/T]GTGATACCCACCCGA	22937
rs781547584	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47442750	ACTCACAGTTATAAG[A/G]AGCCCAAGCTCCCAT	22937
rs781565109	snp	A/C/T	3.38228e-05	0.00411223	missense	SCAP	GRCh38.p7	3:47414934	GGGTCAGGTGACAGG[A/C/T]CACTGTGTCGCTGCT	22937
rs781594936	snp	A/C			intron-variant, upstream-variant-2KB	SCAP, LOC105377073	GRCh38.p7	3:47474745	AAGGCTGCAGTGAGC[A/C]GAGATCGCGCCACTG	22937
rs781644993	snp	A/T			intron-variant	SCAP	GRCh38.p7	3:47432849	TATTGTCCCTTTGGA[A/T]ACCATCCTCTCTCAT	22937
rs781689777	snp	C/T	1.65658e-05	0.00287795	synonymous-codon, intron-variant, utr-variant-5-prime	SCAP	GRCh38.p7	3:47425556	CAGCGAGCTGAGCAC[C/T]GTGACCACGGCAGCC	22937
rs781725132	snp	C/T	1.71185e-05	0.00292557	intron-variant, upstream-variant-2KB	SCAP	GRCh38.p7	3:47425654	CGGCCCCTCCCCCAG[C/T]CCCCGGCCCACTGGG	22937
rs781758150	in-del	-/T			intron-variant	SCAP	GRCh38.p7	3:47462527	TGACCATAAAGACAC[-/T]TATGCTGAAATGAGA	22937
rs781760076	snp	C/G	1.72113e-05	0.00293348	intron-variant, utr-variant-3-prime, downstream-variant-500B	PTPN23, SCAP	GRCh38.p7	3:47413810	CAGTGCATTGGCCCC[C/G]ACACAGCACCCCAGC	22937
rs796088426	in-del	-/A			intron-variant	SCAP	GRCh38.p7	3:47465768	GCAAGACTCCGTCTC[-/A]AAAAAAAAAAAAAGA	22937
rs796107823	multinucleotide-polymorphism	CT/TC			intron-variant	SCAP	GRCh38.p7	3:47443306	TCTCTCTCTCTCTCT[CT/TC]CTCCCTCCCCGCCCA	22937
rs796469858	snp	C/T			intron-variant	SCAP	GRCh38.p7	3:47459550	AGGGGTGACATCACA[C/T]ATGAGTAGGACCGTG	22937
rs796511709	in-del	-/A			intron-variant	SCAP	GRCh38.p7	3:47465841	CTTGTTTAAAAAAAC[-/A]AAAAAAAAAAAAGCT	22937
rs796569600	in-del	-/ACT			intron-variant	SCAP	GRCh38.p7	3:47436787	GTGTATATCTGTGTA[-/ACT]ACTATCTAGATCAAG	22937
rs796601479	in-del	-/T			intron-variant	SCAP	GRCh38.p7	3:47465168	TGGAAGATGATATTC[-/T]TTTTTTTTTTTTCTT	22937
rs796750971	in-del	CT/TCTCTC			intron-variant	SCAP	GRCh38.p7	3:47443302	TCTCTCTCTCTCTCT[CT/TCTCTC]CTCCCTCCCCGCCCA	22937
rs796762791	snp	A/G			intron-variant	SCAP	GRCh38.p7	3:47414655	CCAGACGGAACACCT[A/G]GGACAGGGATGGGCC	22937
rs796866428	in-del	-/A			intron-variant	SCAP	GRCh38.p7	3:47455052	TCCAAATATATATAC[-/A]AAAAAATTACATATA	22937

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