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

ASB11

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs755521735	snp	A/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15287823	AATGCTACAGATGAG[A/T]CAGGAAGGGGAGAGA	140456
rs755661723	snp	A/G	0.000529661	0.016265			GRCh38.p7	X:15275913	ATCCATGCAAGTGCC[A/G]CCCCTGGCAGTGATA	140456
rs755700466	snp	A/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15310768	CAAGGCAGGTGGATA[A/G]CCTAAGGTCAGGAGT	140456
rs755831077	snp	C/T			intron-variant	ASB11	GRCh38.p7	X:15304230	AATAACTGAAGGCCT[C/T]AAGGAAAGAAAGAAT	140456
rs755860070	snp	A/G	0.000529661	0.016265			GRCh38.p7	X:15280814	CAGATGTGGAGAAAA[A/G]GGAATTCTTATACAC	140456
rs755868973	snp	C/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15292974	CGAAGTTATAAGTAG[C/G]GCTCTTTTGTGCCAC	140456
rs755875255	snp	C/T			intron-variant	ASB11	GRCh38.p7	X:15287253	TTACAAAGCAGAGTT[C/T]TGGTTTGCTCAATCA	140456
rs755897897	snp	C/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15302602	GTATGAGAGGACATA[C/T]GTGCCTCGAATGGCA	140456
rs755900502	snp	A/G			intron-variant	ASB11	GRCh38.p7	X:15297060	GCACTTTGGGAGGCC[A/G]AGGCAGGTGGATCAC	140456
rs756025223	snp	C/G	0.000529661	0.016265	upstream-variant-2KB	ASB11	GRCh38.p7	X:15315755	ACTGATTTGGCGACT[C/G]CATGTGCTGACTCCA	140456
rs756058926	snp	A/G	0.00158814	0.0281345	intron-variant	ASB11	GRCh38.p7	X:15285878	GGCGTGGTGGCACGC[A/G]CCTGTAATCGCAGCT	140456
rs756094429	snp	A/G	2.28786e-05	0.00338212	missense, intron-variant	ASB11	GRCh38.p7	X:15314438	CGGACCTTCTGATAC[A/G]TTCTGAAACTTCACA	140456
rs756108991	snp	G/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15306866	GTACTTCAGACATGT[G/T]ACGCTCTTGCCTAGT	140456
rs756117062	snp	G/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15303646	CCAGTGGAGCCAGAC[G/T]GCTAGGGTTCAAGTC	140456
rs756130226	snp	C/T	0.000529661	0.016265			GRCh38.p7	X:15280015	GGGTGATTAGCATAT[C/T]CATCACCTCAATCAT	140456
rs756213002	snp	A/T	0.000108961	0.00738027	intron-variant	ASB11	GRCh38.p7	X:15297729	TTTTACAGACTGGGG[A/T]CTCACTGTGTTGCCC	140456
rs756254546	snp	C/T	0.00211696	0.0324653	intron-variant	ASB11	GRCh38.p7	X:15284088	AAACCCCGTGTCCAC[C/T]AAAAATACAAAAAAT	140456
rs756260861	snp	C/T			intron-variant	ASB11	GRCh38.p7	X:15308947	TTTGAGATGGAGTCT[C/T]GCTCTGTCCCCTAGG	140456
rs756279227	snp	A/G			synonymous-codon	ASB11	GRCh38.p7	X:15293258	CACATTGACACATGC[A/G]GCACTGCCGCTGCAG	140456
rs756352756	in-del	-/TAGA/TAGATAGA			intron-variant	ASB11	GRCh38.p7	X:15305597	AAGAAAAAAAAAGAT[-/TAGA/TAGATAGA]TAGATAGATAGATAG	140456
rs756360960	snp	A/G	2.38857e-05	0.00345576	intron-variant	ASB11	GRCh38.p7	X:15289472	TCAACAAAGTTAACA[A/G]GTTTCTTCATGAAAA	140456
rs756414788	snp	C/G					GRCh38.p7	X:15277914	TTCTGAATGTCAGAA[C/G]ACCAAAAATGCCACC	140456
rs756420405	snp	C/T	0.00475684	0.0485365	intron-variant	ASB11	GRCh38.p7	X:15312728	CCCAACAAACATTTG[C/T]CTGACCAGTGCAAAA	140456
rs756456206	snp	C/T	0.00211696	0.0324653	intron-variant	ASB11	GRCh38.p7	X:15296704	TGTTCATTTAAGGTG[C/T]TGAATTAAGAGTGTT	140456
rs756483853	snp	A/G	0.00158814	0.0281345	intron-variant	ASB11	GRCh38.p7	X:15287029	GAATTTCAGATGCTC[A/G]CCTTACCTCTTCTGG	140456
rs756502440	in-del	-/CTCG	0.000529661	0.016265	utr-variant-3-prime	ASB11	GRCh38.p7	X:15281944	GTGCGATCTGCCTGC[-/CTCG]CTCGGCCTCCCAAAA	140456
rs756604657	snp	A/T					GRCh38.p7	X:15276328	TTATTTTTTATTTTT[A/T]TTTTTTGAGACGTAG	140456
rs756626882	snp	A/G	2.31479e-05	0.00340197	upstream-variant-2KB, synonymous-codon	ASB11	GRCh38.p7	X:15315489	ATTTCCTTTGACGAT[A/G]TAGAAATGGGTTAGG	140456
rs756651281	snp	A/G			intron-variant	ASB11	GRCh38.p7	X:15295321	GCTGGGATTACAGGC[A/G]TGAGCCACTGTGCCT	140456
rs756663647	snp	A/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15291885	ACTAAAAATACAAAA[A/G]TTAGCCAATTGTGGT	140456
rs756706112	snp	C/G	0.000529661	0.016265	upstream-variant-2KB	ASB11	GRCh38.p7	X:15316719	ACCTCAGGTGATCCA[C/G]CCACTTTGGCCTCCC	140456
rs756730250	snp	A/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15301509	CATACACATGCACAC[A/G]CAGACAGAGAGAGAG	140456
rs756807071	snp	C/T	0.000529661	0.016265	utr-variant-3-prime	ASB11	GRCh38.p7	X:15282975	GTGTGTGTATATATA[C/T]ACGTATATATATATA	140456
rs756923249	snp	C/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15301094	CAGCCTCCCAAGTAG[C/G]TGGGATTATAGGCGC	140456
rs756939281	snp	A/G	2.31578e-05	0.0034027	missense, intron-variant	ASB11	GRCh38.p7	X:15297659	GACACCCGGTTAATT[A/G]TCACAAGGTTCACAT	140456
rs756971681	snp	C/T			intron-variant	ASB11	GRCh38.p7	X:15289761	GGGTGTGGTGGCTCA[C/T]GCCTGTAATCTCAGC	140456
rs757032478	snp	C/G			utr-variant-3-prime	ASB11	GRCh38.p7	X:15283169	TGAATTTATATGTGT[C/G]TATACAATATTCAGA	140456
rs757035178	snp	C/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15309633	GGTTGGGGACCACTG[C/T]TATAAATGGTGTGAA	140456
rs757131031	snp	A/C/G	7.4114e-05	0.00608707	intron-variant	ASB11	GRCh38.p7	X:15297546	GCATCTGGCCAGACA[A/C/G]ACCCAAGTGGGCAGG	140456
rs757138807	snp	C/G/T	0.000139598	0.00835342	missense, intron-variant	ASB11	GRCh38.p7	X:15297648	CGTGGAGAGAAGACA[C/G/T]CCGGTTAATTGTCAC	140456
rs757182711	snp	A/C	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15314310	ATCATGCTTAACTTG[A/C]AACTTATCAGAAGCA	140456
rs757203355	snp	A/C	0.000529661	0.016265	upstream-variant-2KB, intron-variant	ASB11	GRCh38.p7	X:15314760	TATCTGACTCATTTA[A/C]TTTTGTAGCATCTCA	140456
rs757344399	snp	A/G	4.58668e-05	0.00478866	synonymous-codon, intron-variant	ASB11	GRCh38.p7	X:15314454	TTCTGAAACTTCACA[A/G]TTCTTCTCATTTTCC	140456
rs757404474	snp	A/G			intron-variant	ASB11	GRCh38.p7	X:15295546	CACCAGGCCTCTGAA[A/G]CTAGGAACCCAAGAT	140456
rs757424476	snp	A/G					GRCh38.p7	X:15278081	CCACTTCCCTAACCC[A/G]TAAATATAGCTAAGG	140456
rs757465967	snp	A/G			intron-variant	ASB11	GRCh38.p7	X:15311174	GATATCTAAAATATT[A/G]TAATAAAACTGAGTT	140456
rs757539344	snp	C/T	2.34381e-05	0.00342323	intron-variant	ASB11	GRCh38.p7	X:15302846	GTCAAGGCCTGGAGA[C/T]TTCTTCCTGTAACTT	140456
rs757577028	snp	C/T			intron-variant	ASB11	GRCh38.p7	X:15288923	TTTTCCACGGACTCT[C/T]GGTTTCTGTATATGC	140456
rs757581613	snp	G/T	0.00105904	0.0229869	intron-variant	ASB11	GRCh38.p7	X:15295200	GGCGCGTGCCACCAT[G/T]CCTAGCTAGTTTTTG	140456
rs757592691	snp	G/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15288960	GAATTGCTTTTAAAA[G/T]GACTAGATACTGTAG	140456
rs757595068	snp	C/T			intron-variant	ASB11	GRCh38.p7	X:15293586	TCCATTTTCCATTTT[C/T]CATTAATATGACTCC	140456
rs757616749	snp	A/G			intron-variant	ASB11	GRCh38.p7	X:15304467	AAAACATAGATGTGC[A/G]TATATACGTATTTTT	140456
rs757637373	snp	C/T			intron-variant	ASB11	GRCh38.p7	X:15305764	TCATCAATTTTATGT[C/T]TTTTGACTTTTATCT	140456
rs757644935	snp	A/G	2.34324e-05	0.00342281	intron-variant	ASB11	GRCh38.p7	X:15289674	CTCACTCAAGTAAGG[A/G]ACATATTAAATATTA	140456
rs757648759	snp	C/T	0.000529661	0.016265			GRCh38.p7	X:15276417	CGCCTCCCGAGTTCA[C/T]GCCATTCTCCTGCCT	140456
rs757735312	in-del	-/A	0.499981	0.0030463	intron-variant	ASB11	GRCh38.p7	X:15312508	TTAAATGCAGCTTCC[-/A]AAAAAAAAAAAAAAA	140456
rs757762774	snp	C/T	2.30351e-05	0.00339367	synonymous-codon	ASB11	GRCh38.p7	X:15289520	TAATTCTAGAAGTTT[C/T]TTCACACAGTCTACC	140456
rs757825078	snp	G/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15303398	AAAATTTATGAATTT[G/T]TGTTGGGCCACATTC	140456
rs757861713	snp	C/T	0.00105904	0.0229869	intron-variant	ASB11	GRCh38.p7	X:15308677	CATGGCTAGGAAGTA[C/T]CAGAAATAGGACTGA	140456
rs757865083	snp	A/G			intron-variant	ASB11	GRCh38.p7	X:15300635	TGGAACAGAAATAGG[A/G]CATGAGAGGAAAAAC	140456
rs757976866	snp	A/G	0.00105904	0.0229869	utr-variant-3-prime	ASB11	GRCh38.p7	X:15281911	CCATAGTGGCCAGGC[A/G]GTTCTCGAACTCCTG	140456
rs758034600	snp	A/T	0.00105904	0.0229869	intron-variant	ASB11	GRCh38.p7	X:15286888	CCCAGTGCCTGGCAT[A/T]CGTAGAGCTGAATAA	140456
rs758085948	snp	A/T	0.00158814	0.0281345	intron-variant	ASB11	GRCh38.p7	X:15314141	CAACAGGAGAAAACA[A/T]TTGTAACATGTTCTT	140456
rs758089252	snp	C/T	4.55809e-05	0.00477372	synonymous-codon	ASB11	GRCh38.p7	X:15283508	GAACACTTAGGACTA[C/T]TGGTATAGGAGGAAT	140456
rs758145043	snp	A/G	2.28663e-05	0.00338122	missense	ASB11	GRCh38.p7	X:15302787	CAGCTTCATGAAGTG[A/G]GGATCGATCAGCCCA	140456
rs758173236	snp	C/T	0.00105904	0.0229869	downstream-variant-500B	ASB11	GRCh38.p7	X:15281282	TATGTATTTTACACG[C/T]GCAACACATCTTAAT	140456
rs758176882	snp	G/T	0.00158814	0.0281345	intron-variant	ASB11	GRCh38.p7	X:15284209	GTGAGCCGAGATCGG[G/T]CCACTGCACTCCAGC	140456
rs758198880	snp	A/G			intron-variant	ASB11	GRCh38.p7	X:15286836	CTGCTCTAAAGTTTT[A/G]AAAATTCAGTGAGCT	140456
rs758239487	snp	A/T			intron-variant	ASB11	GRCh38.p7	X:15309021	TCCCAGGTTCAAGAG[A/T]TTCTCTGGCCTCAGC	140456
rs758306804	snp	A/G			intron-variant	ASB11	GRCh38.p7	X:15285096	CCAGTGCCCAGAGAC[A/G]CTGACAGGAGAGTGA	140456
rs758373246	snp	A/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15291726	AATAAAAAAAAAATT[A/T]AAAAAAATTAAAAAA	140456
rs758392840	snp	C/T					GRCh38.p7	X:15280794	GAAAATAACAAATGC[C/T]GGTGCAGATGTGGAG	140456
rs758397580	snp	C/T			intron-variant	ASB11	GRCh38.p7	X:15302067	CAACTGTGACTTCCT[C/T]CTTAGGTACCTCTTG	140456
rs758430401	snp	C/T	2.31471e-05	0.00340191	missense, intron-variant	ASB11	GRCh38.p7	X:15297674	GTCACAAGGTTCACA[C/T]TGACACCCTATAATT	140456
rs758496883	snp	C/T	0.00528398	0.051128	intron-variant	ASB11	GRCh38.p7	X:15297446	GCCTAAATGATGGAA[C/T]ACGGACATGGATAGA	140456
rs758506121	snp	C/T			utr-variant-3-prime	ASB11	GRCh38.p7	X:15282452	ATTTTGGGCCCCTAT[C/T]CACAGAAAAAAATAT	140456
rs758588499	snp	A/G			intron-variant	ASB11	GRCh38.p7	X:15296886	ATACCCAGAAGAAAG[A/G]AAAACAGTATATCCA	140456
rs758613491	snp	A/G	2.38572e-05	0.0034537	upstream-variant-2KB, missense	ASB11	GRCh38.p7	X:15315454	TAGATCTCTTCTGCT[A/G]TCCTAGCCGCTTCTT	140456
rs758624814	snp	C/T	2.29508e-05	0.00338746	missense, intron-variant	ASB11	GRCh38.p7	X:15314459	AAACTTCACAATTCT[C/T]CTCATTTTCCCCAGT	140456
rs758673792	snp	C/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15305313	CCCAAAATGCATAAC[C/T]AAAATCTGATAAGGA	140456
rs758684680	snp	C/T			intron-variant	ASB11	GRCh38.p7	X:15307231	CTCAAGTCATATACA[C/T]AACATGGATAAATCT	140456
rs758714896	snp	A/C/G/T	0.000182325	0.00954643	missense	ASB11	GRCh38.p7	X:15283602	TTCCGGACACACAGG[A/C/G/T]GGCAGAGCTGGGAAA	140456
rs758718843	snp	A/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15296988	TCCACCAACAGATGA[A/G]TGCATAAAGAAAACA	140456
rs758775221	snp	C/T			intron-variant	ASB11	GRCh38.p7	X:15290744	TAGATAACATAAAAG[C/T]AAGCTTCATTTTAGA	140456
rs758785429	snp	C/G	0.0251071	0.109193			GRCh38.p7	X:15276387	AGTGGTGCGATCTTG[C/G]CTCACTGCAAGCTCC	140456
rs758799291	in-del	-/AAAAAA	0.442425	0.159602	intron-variant	ASB11	GRCh38.p7	X:15309967	GCAAGACTCCGTCTC[-/AAAAAA]AAAAAAAAAAAAAAA	140456
rs758855699	snp	C/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15294304	TTCAACAACTAAGGA[C/T]GCATGCTTGTGATAA	140456
rs758878984	snp	C/T	0.00166224	0.0287817	missense	ASB11	GRCh38.p7	X:15283579	GATGACATGCTCGAC[C/T]GAGACACTTCCGGAC	140456
rs758944714	in-del	-/A			intron-variant	ASB11	GRCh38.p7	X:15284371	GAACAGAGGGACAAT[-/A]ACGGAAAGGGTGTCA	140456
rs758952078	snp	C/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15304789	CTGAGGCAGAAGAAT[C/T]GCTTGAACCCGGGAG	140456
rs759000536	snp	A/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15310864	TGGTGGCGGGCGCCT[A/G]TACTCCCAGCTACTC	140456
rs759035082	snp	A/G	0.00105904	0.0229869			GRCh38.p7	X:15276613	TGAGCCACTGCGCCC[A/G]GCCTATTTTTTTTAA	140456
rs759066460	snp	C/T			intron-variant	ASB11	GRCh38.p7	X:15296117	AGCTGGACGTGGTGG[C/T]GGGCACCTGTAATCC	140456
rs759076290	snp	G/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15295858	TCCAGTCATCTAGCT[G/T]GAAAGGAAACGGCTC	140456
rs759132310	snp	A/G			intron-variant	ASB11	GRCh38.p7	X:15304225	TTTGAAATAACTGAA[A/G]GCCTTAAGGAAAGAA	140456
rs759143340	snp	A/G					GRCh38.p7	X:15277599	CCCCAAACCGCAGGC[A/G]AAATGGAAACTGAAG	140456
rs759150211	snp	A/G	2.40819e-05	0.00346992	synonymous-codon	ASB11	GRCh38.p7	X:15287888	TTGGTTACCTTCACG[A/G]AGCAAGAGTGCCTGC	140456
rs759155699	snp	G/T			intron-variant	ASB11	GRCh38.p7	X:15288162	CATATAAAGACATTT[G/T]AAGTACCATGACATA	140456
rs759186638	snp	A/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15284167	TGAGGCAGGAGAATG[A/G]CGTGAACCCGGGAGG	140456
rs759237773	in-del	-/A	0.000122862	0.00783684	splice-donor-variant	ASB11	GRCh38.p7	X:15297571	GCAGGGGCAGTACTC[-/A]ACGTGTGCACCATTT	140456
rs759271939	snp	G/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15309364	TCCTTATGAGTCTAA[G/T]GCCTGATGATCTGTC	140456
rs759277106	snp	A/G/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15304226	TTGAAATAACTGAAG[A/G/T]CCTTAAGGAAAGAAA	140456
rs759333326	snp	C/T	2.50589e-05	0.00353961	upstream-variant-2KB, intron-variant	ASB11	GRCh38.p7	X:15315390	TCTAGGAGGGATTTT[C/T]TTTAAATATTAGGAA	140456
rs759497063	snp	A/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15287479	CTACAGGCGCCAGCC[A/G]CCACATCTGGCTAAT	140456
rs759509349	snp	C/T			intron-variant	ASB11	GRCh38.p7	X:15305225	TCATCTGATGGAATG[C/T]GATGAGCAACATCAT	140456
rs759537917	snp	C/T	0.00105904	0.0229869	intron-variant	ASB11	GRCh38.p7	X:15308363	GTGCCATCTTTCATT[C/T]CACCAAGAAAGAGGG	140456
rs759594699	snp	A/G			intron-variant	ASB11	GRCh38.p7	X:15301619	CCAGATGATTGCCTA[A/G]TTGTGGAAGAAAGAC	140456
rs759602459	snp	C/T			intron-variant	ASB11	GRCh38.p7	X:15285877	GGGCGTGGTGGCACG[C/T]GCCTGTAATCGCAGC	140456
rs759622520	snp	A/T			upstream-variant-2KB, intron-variant	ASB11	GRCh38.p7	X:15315336	AAAATCAAAGTATAA[A/T]TATAATCTGCCTTCC	140456
rs759639044	snp	A/G			intron-variant	ASB11	GRCh38.p7	X:15284616	TGTTCCCTGAAACTG[A/G]GTCTCATGGACTCTC	140456
rs759639344	snp	A/T	0.000529661	0.016265			GRCh38.p7	X:15275560	TATATATGCATGTAC[A/T]TGTATATACATACAT	140456
rs759691743	in-del	-/G			utr-variant-3-prime	ASB11	GRCh38.p7	X:15281711	CTTTTTTTTTTTTTT[-/G]TTTTGAGACGGAGTC	140456
rs759707963	in-del	-/TATAAA	0.000529661	0.016265	upstream-variant-2KB, intron-variant	ASB11	GRCh38.p7	X:15315331	CACTTAAAATCAAAG[-/TATAAA]TATAATCTGCCTTCC	140456
rs759717776	snp	C/G			intron-variant	ASB11	GRCh38.p7	X:15300222	TGTGATGCTGGAAAG[C/G]CCTGAAAGATCATCT	140456
rs759726773	snp	G/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15292536	ATTTACTATTTTCCT[G/T]CACTTGGAAATTAAC	140456
rs759807376	snp	A/G	0.00105904	0.0229869	intron-variant	ASB11	GRCh38.p7	X:15301923	GCACCCAGTAATCCT[A/G]GAATCCAGGTATTGC	140456
rs759810407	snp	A/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15298242	GTAGTATTTAGCTAA[A/G]ACTTGAAGCATAAAA	140456
rs759826889	snp	A/G			intron-variant	ASB11	GRCh38.p7	X:15312983	TTTTAAGTATTTTGT[A/G]GGGCGGGGGAAGATT	140456
rs759899272	snp	C/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15289355	TGAGAAATACAGACA[C/T]TCATTTCTCTAGAGA	140456
rs759917240	snp	C/T	2.37158e-05	0.00344345	missense	ASB11	GRCh38.p7	X:15293320	CTGTCACTCCATTGA[C/T]CTAATGATGGGCAAA	140456
rs760094945	snp	A/G			intron-variant	ASB11	GRCh38.p7	X:15305421	AAGGGATGACGAAAC[A/G]CGCTATCTAAAGGCA	140456
rs760107192	snp	A/G	2.35338e-05	0.00343021	synonymous-codon, intron-variant	ASB11	GRCh38.p7	X:15297634	TCCAAGGCATGCCTC[A/G]TGGAGAGAAGACACC	140456
rs760135124	snp	A/G	4.80019e-05	0.00489884	synonymous-codon	ASB11	GRCh38.p7	X:15297613	TTTGGCACAGGCCAC[A/G]TGACCTCCAAGGCAT	140456
rs760195110	snp	C/T			utr-variant-3-prime	ASB11	GRCh38.p7	X:15281933	GAACTCCTGACAGTG[C/T]GATCTGCCTGCCTCG	140456
rs760205146	snp	C/T	0.00158814	0.0281345	intron-variant	ASB11	GRCh38.p7	X:15303213	ACCCCAAAGACTCAA[C/T]AGCCTGTGTATTATG	140456
rs760273362	snp	C/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15284007	CCTGTAATCCCAGCA[C/G]TTTGGGAGGCCAAGG	140456
rs760273491	in-del	-/CT	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15290015	GCCGACAAAGCGAGA[-/CT]CTGTCTCAAAATAAA	140456
rs760369784	multinucleotide-polymorphism	CA/GG			intron-variant	ASB11	GRCh38.p7	X:15284048	ACGAGGTCAGGAGAT[CA/GG]AGACCATCCTGGCTA	140456
rs760394356	snp	C/T	0.00158814	0.0281345	upstream-variant-2KB	ASB11	GRCh38.p7	X:15317127	AGTTTTCCTCATCAC[C/T]CTAGGTCTCTGCCTT	140456
rs760402919	in-del	-/A			intron-variant	ASB11	GRCh38.p7	X:15314057	GCGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA	140456
rs760467867	snp	C/T	7.09052e-05	0.00595379	missense	ASB11	GRCh38.p7	X:15287908	AGAGTGCCTGCTCCA[C/T]GCTGCTTTTTGGAGC	140456
rs760478030	snp	C/T			upstream-variant-2KB	ASB11	GRCh38.p7	X:15317614	ATAACATTATTCAAT[C/T]TTGTTTTGGTCTTTT	140456
rs760486028	snp	G/T	0.00158814	0.0281345	intron-variant	ASB11	GRCh38.p7	X:15308295	ACTGCAGCATCCTCT[G/T]ATGTCCCCAACTCTG	140456
rs760517409	snp	A/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15286567	CTACTCAGGAGGCTG[A/G]GGCAGAAAAATCGCT	140456
rs760537473	in-del	-/AAAT	0.0159363	0.0878305	intron-variant	ASB11	GRCh38.p7	X:15290025	CGAGACTCTGTCTCA[-/AAAT]AAATAAATAAATAAA	140456
rs760566017	snp	A/G	2.46734e-05	0.00351228	upstream-variant-2KB, intron-variant	ASB11	GRCh38.p7	X:15315415	TAGGAACAAATTCAT[A/G]TACTTTTACCTGAAA	140456
rs760587692	snp	A/G	2.32591e-05	0.00341013	upstream-variant-2KB, missense	ASB11	GRCh38.p7	X:15315547	TTAAAGAAAAAAAAC[A/G]TAGCAAACATTGTAA	140456
rs760611981	snp	G/T					GRCh38.p7	X:15275497	ATATGTGTATACATT[G/T]GTATATGCATATGTA	140456
rs760661272	in-del	-/TTAA	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15291321	GCACTGCAGACATAC[-/TTAA]TTAATTCAAACCATT	140456
rs760796127	snp	A/G	0.0465453	0.14528	intron-variant	ASB11	GRCh38.p7	X:15301232	CCTCCTAAAGTGCTA[A/G]GATTACAGGCGTGAG	140456
rs760816910	snp	C/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15292385	TTTCTGATCTCAGTA[C/T]AAGAGAACAACTCCC	140456
rs760832452	snp	G/T	4.84373e-05	0.00492101	intron-variant	ASB11	GRCh38.p7	X:15293157	TTCACATGCATTGTG[G/T]TGGCTCATTTACCTC	140456
rs760845623	snp	A/G			intron-variant	ASB11	GRCh38.p7	X:15285962	GTGAGCCGAGATCAC[A/G]CCACTGCACTCCAGC	140456
rs760853110	snp	C/T			intron-variant	ASB11	GRCh38.p7	X:15310892	CTCAGCAGGCTGAGG[C/T]AGGAGAATCACTTGA	140456
rs761030009	snp	A/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15297289	GTGAGACTCCGTCTC[A/G]AAAACAAAACAAAAC	140456
rs761123090	snp	A/G/T	0.000172905	0.00929667	intron-variant	ASB11	GRCh38.p7	X:15297547	CATCTGGCCAGACAG[A/G/T]CCCAAGTGGGCAGGG	140456
rs761126982	snp	A/C	0.000161125	0.00897422	synonymous-codon, intron-variant	ASB11	GRCh38.p7	X:15314397	GTGACAAATATAATC[A/C]CCAAAAGAAATCTCT	140456
rs761212637	snp	C/T			intron-variant	ASB11	GRCh38.p7	X:15290635	CTTCTGAGGTATTGA[C/T]GGGAGCTTGCAAAGA	140456
rs761283725	snp	A/G	2.2804e-05	0.00337661	utr-variant-3-prime	ASB11	GRCh38.p7	X:15283479	AATCTGTGTCATTCC[A/G]AGTATCTTCCCAGGA	140456
rs761297306	snp	A/G			intron-variant	ASB11	GRCh38.p7	X:15308088	AGTGCCTTGGGAGTG[A/G]GGAGAAACAAGAGGG	140456
rs761350372	in-del	-/CTGT	0.00105904	0.0229869	intron-variant	ASB11	GRCh38.p7	X:15310590	TCAGATGGAGTACAG[-/CTGT]CTAAGTTCCAACCAT	140456
rs761478838	snp	C/G					GRCh38.p7	X:15277089	ATACTTTTATAATAG[C/G]ATATCTATGTTAAAT	140456
rs761505872	snp	A/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15288689	AGGAGTTCGAGACCA[A/G]CCTGGCCAACATGGT	140456
rs761523446	snp	A/G			intron-variant	ASB11	GRCh38.p7	X:15301765	CAAGGTGCTGGGGAT[A/G]TAGTCATAAATATAA	140456
rs761539521	snp	A/C	0.000529661	0.016265	upstream-variant-2KB	ASB11	GRCh38.p7	X:15316388	CTCCAGCCTGGGTGA[A/C]AAGAGCAAGATTCTG	140456
rs761586626	snp	C/T	0.0282	0.115346			GRCh38.p7	X:15276377	GCTGGAGTGCAGTGG[C/T]GCGATCTTGGCTCAC	140456
rs761604759	snp	C/T	2.35688e-05	0.00343276	upstream-variant-2KB, missense	ASB11	GRCh38.p7	X:15315563	TAGCAAACATTGTAA[C/T]AAAAATGTTTTTAAA	140456
rs761617786	snp	C/T	2.28566e-05	0.0033805	missense	ASB11	GRCh38.p7	X:15302762	AGGGCCAGTAAGCGC[C/T]CCTGAGCTGCAGCTT	140456
rs761625808	snp	C/T			intron-variant	ASB11	GRCh38.p7	X:15297208	GAGGCAGGAGAATGG[C/T]GTGAACCCCGGCAGA	140456
rs761662133	snp	C/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15294865	GAAGTTGTCTTCTTA[C/T]GCGATTTCCTATAAA	140456
rs761678439	snp	A/G	0.00158814	0.0281345	intron-variant	ASB11	GRCh38.p7	X:15285864	CAAAAAATTAGCTGG[A/G]CGTGGTGGCACGCGC	140456
rs761705164	snp	A/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15293912	GAGGGGGGAGGGATA[A/G]CATTAGGATGTAAAT	140456
rs761707523	snp	C/T	2.3362e-05	0.00341767	missense	ASB11	GRCh38.p7	X:15288061	GCCACTGGCCATGGT[C/T]GACACTGGCTCCTTA	140456
rs761760041	snp	A/G					GRCh38.p7	X:15275662	GTGAATTGAGGTGAT[A/G]GGCATACAGATATTA	140456
rs761891594	snp	A/G	0.00105904	0.0229869	intron-variant	ASB11	GRCh38.p7	X:15303047	ATCTCTCTGGCTTTT[A/G]GGAGGCAATTTTAAT	140456
rs761901662	snp	C/T	2.38903e-05	0.00345609	synonymous-codon	ASB11	GRCh38.p7	X:15293177	TCATTTACCTCTCTT[C/T]ACTGCCTCATGGATG	140456
rs761937987	snp	A/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15308190	GCAGGCCTCACTCCA[A/G]GTCTGTGGCATGCCC	140456
rs761969743	snp	G/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15299802	CCAGCCGAGTCCTGC[G/T]TTTGATCCTATGCCT	140456
rs761979340	snp	G/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15307355	CCACCAAGGACTGGT[G/T]TCATGGAAGACAATT	140456
rs761985655	snp	C/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15290174	GCTTCCCCACTCCAG[C/T]TCCTCTTTACAGCCC	140456
rs761994161	snp	A/G			intron-variant	ASB11	GRCh38.p7	X:15296604	TAAATTTAAAATAAG[A/G]TAAAGTTCAATTCTG	140456
rs762044007	snp	A/G			intron-variant	ASB11	GRCh38.p7	X:15289481	TTAACAGGTTTCTTC[A/G]TGAAAATAATTTTGG	140456
rs762048689	snp	A/G	0.00633741	0.0559334	intron-variant	ASB11	GRCh38.p7	X:15284178	AATGGCGTGAACCCG[A/G]GAGGCGGAGCTTGCA	140456
rs762111472	snp	A/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15313790	GGCGCGGTGGCTCAC[A/G]CCTGTAATCCCAGCA	140456
rs762243251	snp	A/C			utr-variant-3-prime	ASB11	GRCh38.p7	X:15282215	AAAAAACATGTGTGA[A/C]ATGAGTCTTAGGATG	140456
rs762245541	snp	A/G			intron-variant	ASB11	GRCh38.p7	X:15299622	GGAGGAGGGTATAAT[A/G]AGGCATGTTCAACCC	140456
rs762344649	in-del	-/CA			intron-variant	ASB11	GRCh38.p7	X:15313473	GGATTCGTGTATATG[-/CA]TATACACACACACAC	140456
rs762357821	in-del	-/AC	0.00738971	0.0603345	intron-variant	ASB11	GRCh38.p7	X:15291223	GAAAAATATACAGAG[-/AC]ACACAAATTATGTGT	140456
rs762369980	snp	A/G			intron-variant	ASB11	GRCh38.p7	X:15297736	GACTGGGGTCTCACT[A/G]TGTTGCCCAGGCTGG	140456
rs762379602	snp	A/G	0.00317376	0.039709	intron-variant	ASB11	GRCh38.p7	X:15288637	ACCTGTAATCCCAGC[A/G]CTTTGGGAGACTGAG	140456
rs762471967	snp	A/G			intron-variant	ASB11	GRCh38.p7	X:15310165	CTATCCTTGTTCCCA[A/G]CAGAGTCTCTCACTC	140456
rs762564369	snp	A/G	0.00160556	0.0282879	utr-variant-3-prime	ASB11	GRCh38.p7	X:15282966	TGCATGTGTGTGTGT[A/G]TATATATATACGTAT	140456
rs762566030	snp	C/G	2.36563e-05	0.00343913	utr-variant-5-prime, intron-variant	ASB11	GRCh38.p7	X:15314532	CTTTAGATAAGACTG[C/G]TGTTGTCTAGTGTCT	140456
rs762657163	snp	G/T			intron-variant	ASB11	GRCh38.p7	X:15288096	AACAGATGGCCACAA[G/T]TCAACACTAAATGTA	140456
rs762697204	in-del	-/TAACTT	0.492413	0.0611204	intron-variant	ASB11	GRCh38.p7	X:15312837	GATTTTTAATACACC[-/TAACTT]TAAATATATTGTTAT	140456
rs762711834	snp	A/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15296590	AAAAAGTTTGGAGAT[A/G]AATTTAAAATAAGAT	140456
rs762793614	snp	C/T	0.00158814	0.0281345	intron-variant	ASB11	GRCh38.p7	X:15302196	AGTTTGAAAGCAGAT[C/T]CTGCCCGCCTTGAGC	140456
rs762828369	snp	C/T			intron-variant	ASB11	GRCh38.p7	X:15303902	TTCCAGACATATTTT[C/T]CTTATAATTGCTTAT	140456
rs762830625	snp	C/T	0.000529661	0.016265			GRCh38.p7	X:15275669	GAGGTGATGGGCATA[C/T]AGATATTAATTGTTT	140456
rs762835647	snp	G/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15301404	GTTCATTTGATCATT[G/T]CTGGCAGTGCTGATT	140456
rs762838813	in-del	-/CA	0.00317376	0.039709			GRCh38.p7	X:15281089	CAATCCCAGCTACTC[-/CA]GAGGCTGAGGCAGGA	140456
rs762844747	snp	A/G			intron-variant	ASB11	GRCh38.p7	X:15304930	ATTTCAAAATAAACA[A/G]TAAGAGATTATATCT	140456
rs762885115	snp	G/T	0.000529661	0.016265			GRCh38.p7	X:15276287	GTTGAGACTTAAATC[G/T]TCAAGTGACATAGCA	140456
rs762930444	snp	G/T	2.29192e-05	0.00338513	synonymous-codon	ASB11	GRCh38.p7	X:15289616	ATTATTTGCCAGCAG[G/T]ATCTCCATGCACTCT	140456
rs762940447	snp	C/T	0.000529661	0.016265	utr-variant-3-prime	ASB11	GRCh38.p7	X:15283386	ATGGGGGATTTACTT[C/T]GACTGAGCTCATTTA	140456
rs762948059	snp	A/G			intron-variant	ASB11	GRCh38.p7	X:15299872	TGACCCTGAACCCCG[A/G]ACTCCTACTTACACG	140456
rs762985880	snp	C/G	0.00475684	0.0485365	intron-variant	ASB11	GRCh38.p7	X:15285766	CCCTGCACTTTGGGA[C/G]GCTGAGGCGGGTGGA	140456
rs763035352	snp	A/C	0.00105904	0.0229869	upstream-variant-2KB	ASB11	GRCh38.p7	X:15316253	CTCTACTAAAAGTAC[A/C]AAAATTAGCTGGGCG	140456
rs763072464	snp	A/G			intron-variant	ASB11	GRCh38.p7	X:15298171	CCAAAATTAGTTTGG[A/G]AGCATAGGATATCCT	140456
rs763108888	snp	A/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15294753	AAAATGTGTGTAAAT[A/T]TATATTGCTAGGGGT	140456
rs763113020	snp	A/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15285266	CTGCCTCAGCCTCCC[A/G]GGTAGGTGGGATTAC	140456
rs763148786	snp	C/T	2.31457e-05	0.00340181	upstream-variant-2KB, missense	ASB11	GRCh38.p7	X:15315490	TTTCCTTTGACGATA[C/T]AGAAATGGGTTAGGA	140456
rs763149284	snp	C/T	0.000529661	0.016265			GRCh38.p7	X:15280444	TTATCCATTGATCTG[C/T]TGACAGACATTTAAG	140456
rs763157339	snp	A/G	0.0214859	0.101397	intron-variant	ASB11	GRCh38.p7	X:15312466	GTTTTACAGCACAAA[A/G]AATGATATTTAATGA	140456
rs763201170	snp	A/G			upstream-variant-2KB	ASB11	GRCh38.p7	X:15315942	GGTTGGAAAGATAGA[A/G]ACTTCTTGGCTTCCA	140456
rs763315935	snp	C/T	2.36038e-05	0.00343531	synonymous-codon	ASB11	GRCh38.p7	X:15293312	TCCGTGAACTGTCAC[C/T]CCATTGACCTAATGA	140456
rs763326282	snp	A/C	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15313244	TCTCTACTAAAAATA[A/C]AAAAATTAGCCGGGC	140456
rs763349161	snp	C/G			intron-variant	ASB11	GRCh38.p7	X:15285598	TAAACTATAGTCTCT[C/G]CTAACAGTTGGAAAG	140456
rs763443756	in-del	-/TA	0.0215028	0.101435	utr-variant-3-prime	ASB11	GRCh38.p7	X:15282966	GCATGTGTGTGTGTG[-/TA]TATATATATACGTAT	140456
rs763458142	snp	C/G			intron-variant	ASB11	GRCh38.p7	X:15306738	ACAACAACAACAACT[C/G]TTTGGATATTTATAA	140456
rs763546093	snp	A/G			intron-variant	ASB11	GRCh38.p7	X:15290562	TTGAGAGTTTGCCCA[A/G]TAAATAGATAGACAT	140456
rs763590370	in-del	-/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15288642	TAATCCCAGCACTTT[-/G]GGAGACTGAGGAAGG	140456
rs763705026	snp	A/C	0.00211696	0.0324653	intron-variant	ASB11	GRCh38.p7	X:15309548	CACAAGAATCATCCC[A/C]AAACCATCCCCCCAC	140456
rs763708507	snp	C/G	0.00211696	0.0324653	intron-variant	ASB11	GRCh38.p7	X:15287570	GACCTTGTGATCCAC[C/G]CGCCTCAGCCTCCCA	140456
rs763736804	snp	A/G/T	4.57156e-05	0.00478081	missense	ASB11	GRCh38.p7	X:15302760	TAAGGGCCAGTAAGC[A/G/T]CCCCTGAGCTGCAGC	140456
rs763832275	snp	A/C	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15293867	CAGGAAGGGGAACAT[A/C]ACACACCGGGGACTG	140456
rs763902344	snp	C/T					GRCh38.p7	X:15317652	AACATGGCTGTCCTA[C/T]GTTTTACACGCCAAA	140456
rs764015906	snp	C/G	2.31294e-05	0.00340061	intron-variant	ASB11	GRCh38.p7	X:15283664	GGTGTTAACTTCATA[C/G]TGGTGGGAGGTGGGG	140456
rs764030585	snp	C/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15292896	CACCAGCAAAGAGGA[C/T]CTGGAAAGGCCTGCC	140456
rs764086030	snp	A/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15301462	AACACAACTCATAAA[A/G]GAGAAATCAAAAAAC	140456
rs764088043	snp	A/T	7.04953e-05	0.00593656	upstream-variant-2KB, synonymous-codon	ASB11	GRCh38.p7	X:15315561	CGTAGCAAACATTGT[A/T]ATAAAAATGTTTTTA	140456
rs764138211	in-del	-/A			intron-variant	ASB11	GRCh38.p7	X:15314058	GCGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA	140456
rs764198800	snp	A/G	0.000529661	0.016265			GRCh38.p7	X:15275719	GCTGGAAACTTCAAG[A/G]TATAACAACGGTGGG	140456
rs764217510	snp	A/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15298526	GAAATGGAGCACCTA[A/T]GAAGTCTGCTAGGCT	140456
rs764278148	snp	C/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15285272	CAGCCTCCCGGGTAG[C/G]TGGGATTACAGGCGG	140456
rs764279966	snp	G/T	2.29795e-05	0.00338958	missense	ASB11	GRCh38.p7	X:15287937	GCCGCCAGATCAAGC[G/T]CACTTTTGCCCTGAG	140456
rs764362899	snp	C/T	4.63784e-05	0.00481529	intron-variant	ASB11	GRCh38.p7	X:15289655	TGGTGGAACACAAGA[C/T]ACCCTCACTCAAGTA	140456
rs764404522	snp	A/C	2.34849e-05	0.00342665	splice-donor-variant	ASB11	GRCh38.p7	X:15289502	ATAATTTTGGAAATT[A/C]CCTAATTCTAGAAGT	140456
rs764406635	in-del	-/AAT			intron-variant	ASB11	GRCh38.p7	X:15286006	CAAAACTCCGTCTAA[-/AAT]AATAATAATAATAAT	140456
rs764418379	snp	A/G	0.00105904	0.0229869			GRCh38.p7	X:15279368	GGGTGGGATCTGACA[A/G]TCTCCTTTGCCCTAG	140456
rs764457892	snp	C/T	0.00211696	0.0324653			GRCh38.p7	X:15276542	CAGGATGGTCTCGAT[C/T]TCCTGACCTCGTGAT	140456
rs764475773	snp	A/C/T	4.7885e-05	0.00489292	intron-variant	ASB11	GRCh38.p7	X:15289457	TGAAGCTGTAGAAAA[A/C/T]CAACAAAGTTAACAG	140456
rs764486854	snp	G/T	0.00105904	0.0229869	intron-variant	ASB11	GRCh38.p7	X:15313302	TACTCAGGAGGCTGA[G/T]GCACGAGAATTGCTT	140456
rs764550899	snp	C/T			utr-variant-3-prime	ASB11	GRCh38.p7	X:15282151	TCAGTGGGAGTGGGG[C/T]AAAATTGTCTCCAGT	140456
rs764613447	snp	A/C	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15312484	TGATATTTAATGAGG[A/C]ATGTGGTGTTAAATG	140456
rs764660986	snp	C/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15299639	GGCATGTTCAACCCC[C/G]CTTTCCTGTCATGGC	140456
rs764668839	snp	C/G			intron-variant	ASB11	GRCh38.p7	X:15292800	ATAAGCTATTCTTGC[C/G]TACTAAGGACAGAGA	140456
rs764762940	snp	A/G			intron-variant	ASB11	GRCh38.p7	X:15296323	GCATCAGGAAAATTA[A/G]TTTTCACAAGGAAGA	140456
rs764783559	snp	C/T	6.83706e-05	0.00584642	stop-lost	ASB11	GRCh38.p7	X:15283506	AGGAACACTTAGGAC[C/T]ATTGGTATAGGAGGA	140456
rs764796483	snp	A/C	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15304227	TGAAATAACTGAAGG[A/C]CTTAAGGAAAGAAAG	140456
rs764801887	in-del	-/AAAA	0.488319	0.0755258	intron-variant	ASB11	GRCh38.p7	X:15286664	GTGAGACTCCATCTC[-/AAAA]AAAAAAAAAAAAAAA	140456
rs764877543	in-del	-/CATTTT	2.44774e-05	0.0034983	cds-indel	ASB11	GRCh38.p7	X:15297581	TACTCACGTGTGCAC[-/CATTTT]CATTTTCCAATAAGG	140456
rs764932377	snp	C/T			intron-variant	ASB11	GRCh38.p7	X:15290652	GGAGCTTGCAAAGAG[C/T]TAGTTCTCTTTGAAG	140456
rs764934498	snp	A/G			intron-variant	ASB11	GRCh38.p7	X:15308195	CCTCACTCCAGGTCT[A/G]TGGCATGCCCTTCAC	140456
rs764938563	snp	A/T	0.000529661	0.016265			GRCh38.p7	X:15276626	CCAGCCTATTTTTTT[A/T]AAATAAAAGGTAAAG	140456
rs764965101	snp	G/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15301371	AATAAATAAGCAAGT[G/T]ATAAAATCAGGTACA	140456
rs765030440	snp	A/C			intron-variant	ASB11	GRCh38.p7	X:15301831	GTTCCCTGGGGAGTC[A/C]GATTTACCCATTGTC	140456
rs765085810	snp	A/G	0.000529661	0.016265			GRCh38.p7	X:15275643	AGCAAAATGCTAACA[A/G]TTGGTGAATTGAGGT	140456
rs765095102	snp	C/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15309410	CCCTAGATGGGACCA[C/T]CTAGTTGCAGGAAAA	140456
rs765168306	snp	A/C	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15300707	TATCAATGTTAACTT[A/C]GTATTTTTGACTAAT	140456
rs765173933	snp	A/G	0.000485841	0.0155783	synonymous-codon, intron-variant	ASB11	GRCh38.p7	X:15297664	CCGGTTAATTGTCAC[A/G]AGGTTCACATTGACA	140456
rs765212160	snp	A/G	2.33751e-05	0.00341863	synonymous-codon	ASB11	GRCh38.p7	X:15288062	CCACTGGCCATGGTC[A/G]ACACTGGCTCCTTAA	140456
rs765241622	snp	C/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15287498	CATCTGGCTAATTTC[C/T]GTATTTTTAGTAGAG	140456
rs765246484	snp	C/T	0.000529661	0.016265			GRCh38.p7	X:15278998	TCAATATTTGGGGCG[C/T]ATTGAATTGTACCTC	140456
rs765310243	snp	C/T			upstream-variant-2KB	ASB11	GRCh38.p7	X:15315632	CTCTGTATAGGGTCC[C/T]AGGACTGTAAAATTT	140456
rs765320500	snp	C/G	0.000529661	0.016265			GRCh38.p7	X:15278193	GCAAAACCCGTATCA[C/G]AGTGATTGGTTTACT	140456
rs765329054	in-del	-/TTAG			intron-variant	ASB11	GRCh38.p7	X:15305597	CAAGAAAAAAAAAGA[-/TTAG]ATAGATAGATAGATA	140456
rs765331480	snp	G/T	0.00105904	0.0229869	utr-variant-3-prime	ASB11	GRCh38.p7	X:15282774	GTTAACTACAATGTT[G/T]CTGAAGTCCTTAACT	140456
rs765379380	snp	A/C			intron-variant	ASB11	GRCh38.p7	X:15313894	GTCTCTACTAAAAAT[A/C]CAAAAAAATTAGCTG	140456
rs765415719	snp	C/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15292553	ACTTGGAAATTAACT[C/G]ACAACACAGGAGTCT	140456
rs765459429	snp	A/C	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15305917	TTTCCTGATCGTCTC[A/C]CTCCTCCTACCCTCC	140456
rs765470261	snp	A/G	7.09807e-05	0.00595696	intron-variant	ASB11	GRCh38.p7	X:15289690	ACATATTAAATATTA[A/G]CAGAATTATAGGATT	140456
rs765495633	snp	C/T	0.00158814	0.0281345	intron-variant	ASB11	GRCh38.p7	X:15314049	GGCTACAGAGCGAGA[C/T]TCCATCTCAAAAAAA	140456
rs765661219	snp	C/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15297405	AATATTTACACACAG[C/G]GGGGTAAGTTGAAGA	140456
rs765674953	snp	A/G	2.36521e-05	0.00343882	synonymous-codon	ASB11	GRCh38.p7	X:15293186	TCTCTTCACTGCCTC[A/G]TGGATGGGCGAGGCC	140456
rs765677155	snp	A/G	0.00105904	0.0229869	intron-variant	ASB11	GRCh38.p7	X:15288873	CTGGGCAATAAGAGC[A/G]AAACTTCATCTCAAA	140456
rs765742402	snp	C/T			intron-variant	ASB11	GRCh38.p7	X:15297955	GAGAAGTAGAAGTTA[C/T]GATCAGGGGAGCCTA	140456
rs765791267	snp	C/T	0.00475684	0.0485365	intron-variant	ASB11	GRCh38.p7	X:15298340	AGCAACAGGAAGTTA[C/T]TTCCTGTTGCTTCCT	140456
rs765866935	snp	A/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15303958	ATGAGCATTTGAGAA[A/G]TAACCCCCCATTAAA	140456
rs765932453	snp	A/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15312292	TAAAAACCAAAACTA[A/G]TAACAGTCAACCATG	140456
rs765939357	in-del	-/T	0.00158814	0.0281345	intron-variant	ASB11	GRCh38.p7	X:15295049	AAGAATTTTTTTTAA[-/T]TTTTTTATTTTTTAG	140456
rs765954607	snp	C/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15303276	TTGGTTTCCCTGGGC[C/T]GCATTGGAAGGAGTA	140456
rs765982988	snp	C/G			intron-variant	ASB11	GRCh38.p7	X:15293093	GTCACCCTTGAATGA[C/G]TAACACTAGACCATT	140456
rs765995260	snp	G/T	0.00105904	0.0229869	intron-variant	ASB11	GRCh38.p7	X:15284013	ATCCCAGCACTTTGG[G/T]AGGCCAAGGTGGGCG	140456
rs766058768	snp	A/G	0.000529661	0.016265			GRCh38.p7	X:15276380	GGAGTGCAGTGGTGC[A/G]ATCTTGGCTCACTGC	140456
rs766079138	snp	C/T			intron-variant	ASB11	GRCh38.p7	X:15295159	GAGATTCTGCTGCCT[C/T]AGGCTCCCAAGAAGC	140456
rs766087370	snp	A/C	0.0026455	0.0362733	intron-variant	ASB11	GRCh38.p7	X:15284066	GACCATCCTGGCTAA[A/C]ACGGTGAAACCCCGT	140456
rs766152229	snp	G/T	2.28686e-05	0.00338139	missense	ASB11	GRCh38.p7	X:15302789	GCTTCATGAAGTGGG[G/T]ATCGATCAGCCCAGC	140456
rs766245248	snp	C/T	0.000529661	0.016265	upstream-variant-2KB	ASB11	GRCh38.p7	X:15316507	TAAGATGGAGTCTTA[C/T]TCTGTTGCCCAGGCT	140456
rs766313796	snp	A/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15285930	GAATTGCTTGAACCC[A/G]GGAGGCGGAGGTTGC	140456
rs766333558	in-del	-/AAC	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15292391	ATCTCAGTATAAGAG[-/AAC]AACTCCCTCACTTGC	140456
rs766399993	snp	A/C	0.000529661	0.016265			GRCh38.p7	X:15280821	GGAGAAAAGGGAATT[A/C]TTATACACTATTGGT	140456
rs766413011	snp	A/G	4.59047e-05	0.00479064	synonymous-codon	ASB11	GRCh38.p7	X:15287939	CGCCAGATCAAGCGC[A/G]CTTTTGCCCTGAGCA	140456
rs766419156	snp	C/T	0.00105904	0.0229869	intron-variant	ASB11	GRCh38.p7	X:15313975	GAGAATTGCTTCAAC[C/T]GGGACCTGGGAGGCG	140456
rs766515072	snp	A/G	2.37456e-05	0.00344561	upstream-variant-2KB, synonymous-codon	ASB11	GRCh38.p7	X:15315570	CATTGTAATAAAAAT[A/G]TTTTTAAAGCCATAG	140456
rs766529169	snp	A/G	0.00105904	0.0229869	intron-variant	ASB11	GRCh38.p7	X:15284196	GGCGGAGCTTGCAGT[A/G]AGCCGAGATCGGGCC	140456
rs766579173	snp	G/T			intron-variant	ASB11	GRCh38.p7	X:15298227	AACCTTGCAAATGAG[G/T]TAGTATTTAGCTAAG	140456
rs766603679	snp	A/G			intron-variant	ASB11	GRCh38.p7	X:15308610	AGCCTTGCTTTGCTG[A/G]ATGGTAACACCCCAA	140456
rs766626830	snp	C/T	0.000115318	0.00759249	upstream-variant-2KB, missense	ASB11	GRCh38.p7	X:15315457	ATCTCTTCTGCTATC[C/T]TAGCCGCTTCTTTTC	140456
rs766641107	snp	G/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15291440	TAAATTTTTAATAAA[G/T]ACTTTTTGTAATACC	140456
rs766654572	snp	G/T			upstream-variant-2KB	ASB11	GRCh38.p7	X:15317564	CTAAGTAGGCAATCA[G/T]TTAGTCATGTCAGAC	140456
rs766676769	snp	A/G	2.36393e-05	0.00343789	synonymous-codon	ASB11	GRCh38.p7	X:15293315	GTGAACTGTCACTCC[A/G]TTGACCTAATGATGG	140456
rs766739818	in-del	-/T			intron-variant	ASB11	GRCh38.p7	X:15305598	AAGAAAAAAAAAGAT[-/T]AGATAGATAGATAGA	140456
rs766790004	snp	C/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15305084	CTTCAACTCATCTCC[C/T]TGCAAAATAATGACT	140456
rs766870838	snp	A/G	4.64652e-05	0.0048198	missense	ASB11	GRCh38.p7	X:15293206	TGGGCGAGGCCAGGT[A/G]CACCTCCAACTGGGC	140456
rs766883260	snp	C/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15296761	TTAAGCCTCATACAG[C/T]GTTAGTGGGATTATA	140456
rs766894772	snp	A/G	0.000114407	0.00756244	synonymous-codon, intron-variant	ASB11	GRCh38.p7	X:15314424	CTCTTTCCATGGTCC[A/G]GACCTTCTGATACGT	140456
rs766973820	snp	G/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15284618	TTCCCTGAAACTGAG[G/T]CTCATGGACTCTCAA	140456
rs766975933	snp	G/T	0.00475684	0.0485365			GRCh38.p7	X:15277054	TACAATATGGTTTAT[G/T]GGAAAAGCTGGAATC	140456
rs766988468	snp	A/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15283981	CACGGGGCCAGGCAC[A/G]GTGGCTCACGCCTGT	140456
rs767086348	snp	C/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15302531	AAGGAGGGAACTGGG[C/G]TGAAAATGAAGGAGC	140456
rs767092578	snp	A/C/G	0.000120385	0.00775762	intron-variant	ASB11	GRCh38.p7	X:15293340	TGATGGGCAAAGAGA[A/C/G]ACCCAAAGGATTTGT	140456
rs767128463	snp	A/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15288693	GTTCGAGACCAGCCT[A/G]GCCAACATGGTAAAA	140456
rs767243288	snp	C/G	4.97574e-05	0.00498761	upstream-variant-2KB, intron-variant	ASB11	GRCh38.p7	X:15315403	TTCTTTAAATATTAG[C/G]AACAAATTCATGTAC	140456
rs767246443	snp	A/G	2.29634e-05	0.00338839	intron-variant	ASB11	GRCh38.p7	X:15283652	AGAAATAAAAATGGT[A/G]TTAACTTCATAGTGG	140456
rs767262827	in-del	-/AAC	0.0465972	0.145352	intron-variant	ASB11	GRCh38.p7	X:15306704	TGACACTTTGTCTCA[-/AAC]AACAACAACAACAAC	140456
rs767263863	snp	A/G	0.00105904	0.0229869	intron-variant	ASB11	GRCh38.p7	X:15309757	TGGATCACGAGGTCA[A/G]GAGATCGAGACCATC	140456
rs767284349	snp	C/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15310736	CTTATGCCTGTAATC[C/T]CAGCACTTTGGGAGG	140456
rs767326460	snp	C/T			intron-variant	ASB11	GRCh38.p7	X:15305307	TTTCTGCCCAAAATG[C/T]ATAACCAAAATCTGA	140456
rs767456796	snp	A/G	0.00475684	0.0485365	intron-variant	ASB11	GRCh38.p7	X:15293931	TAGGATGTAAATGAC[A/G]AGTTAATGGGTGCAG	140456
rs767477851	snp	A/G	0.000529661	0.016265	upstream-variant-2KB	ASB11	GRCh38.p7	X:15315716	AGTGCTCCTGTTACC[A/G]AGATCTCTGTAGGTT	140456
rs767520795	snp	C/G			intron-variant	ASB11	GRCh38.p7	X:15285927	GGAGAATTGCTTGAA[C/G]CCGGGAGGCGGAGGT	140456
rs767529842	snp	A/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15303052	TCTGGCTTTTGGGAG[A/G]CAATTTTAATAAGCA	140456
rs767623990	snp	C/T			missense	ASB11	GRCh38.p7	X:15289600	CATGGTCAATGTTAA[C/T]ATTATTTGCCAGCAG	140456
rs767662328	snp	C/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15290209	TAACTTTAACTGAAC[C/T]AAGGGCTCCAAGTAG	140456
rs767691471	snp	C/T			intron-variant	ASB11	GRCh38.p7	X:15310446	TCCTGATGAGGTGTA[C/T]GGAAAATGTTCAAGT	140456
rs767708973	snp	C/T	0.000529661	0.016265			GRCh38.p7	X:15280503	GAGCTACAATAAACA[C/T]GGAGGTGCAACTACC	140456
rs767734249	snp	C/T	2.29779e-05	0.00338946	missense	ASB11	GRCh38.p7	X:15289624	CCAGCAGGATCTCCA[C/T]GCACTCTCTGTGACC	140456
rs767786589	snp	C/G			intron-variant	ASB11	GRCh38.p7	X:15284704	AAAATCAGCTGATGA[C/G]AGTCCAGAATATGGT	140456
rs767786956	snp	C/T			intron-variant	ASB11	GRCh38.p7	X:15301738	ATACTTACCAGGCCC[C/T]TACTCATTTTTCAAG	140456
rs767793877	snp	A/C	0.00475684	0.0485365	intron-variant	ASB11	GRCh38.p7	X:15299831	CTTGTAACTGACCAA[A/C]TGAAAGCTTCCAAAA	140456
rs767797182	snp	C/T	0.00105904	0.0229869	downstream-variant-500B	ASB11	GRCh38.p7	X:15281683	TTGTTTGTTTTTCTT[C/T]CTTTCTTTCTTTCTT	140456
rs767818749	in-del	-/AGAA/AGATAGAA			intron-variant	ASB11	GRCh38.p7	X:15305602	AAAAAAAGATTAGAT[-/AGAA/AGATAGAA]AGATAGATAGATAGA	140456
rs767822616	in-del	-/TT			intron-variant	ASB11	GRCh38.p7	X:15285140	GGTATTTAATCTTTC[-/TT]TTTTTTTTTTTTTTT	140456
rs767870189	snp	G/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15296047	AGGAGTCTGAAACCA[G/T]CATCGCTGGTTTCAC	140456
rs767878290	snp	C/T	0.00158814	0.0281345			GRCh38.p7	X:15276773	GGTTATGAAAATATT[C/T]ATTCCTTAAAATGAT	140456
rs767895073	snp	A/G	7.1101e-05	0.005962	missense	ASB11	GRCh38.p7	X:15297627	CGTGACCTCCAAGGC[A/G]TGCCTCGTGGAGAGA	140456
rs767959988	snp	C/T			intron-variant	ASB11	GRCh38.p7	X:15296132	CGGGCACCTGTAATC[C/T]CAGTTACTCAGGAGG	140456
rs767988478	in-del	-/TG					GRCh38.p7	X:15279944	TTGGTATGTAATAAC[-/TG]TATATATTTATGGGG	140456
rs768039220	snp	C/T	2.44221e-05	0.00349435	upstream-variant-2KB, missense	ASB11	GRCh38.p7	X:15315598	TAGAAAACAGGACCA[C/T]CTTCCATTTTGGCTT	140456
rs768070892	snp	C/T	0.00105904	0.0229869	intron-variant	ASB11	GRCh38.p7	X:15289145	AAATCTAGGCCTAAA[C/T]TAATCAATATATTGT	140456
rs768076405	snp	A/G	0.00105904	0.0229869	intron-variant	ASB11	GRCh38.p7	X:15313812	ATCCCAGCACTTTGC[A/G]AGGCCGAGGCGGGCG	140456
rs768112875	snp	A/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15291270	ATATGTTTTATAGGC[A/G]CATAGATACCAAAAG	140456
rs768137701	snp	C/T			intron-variant	ASB11	GRCh38.p7	X:15293136	TTGGAGTGAGCCCAT[C/T]AATGTTTCACATGCA	140456
rs768202492	snp	A/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15284184	GTGAACCCGGGAGGC[A/G]GAGCTTGCAGTGAGC	140456
rs768206874	snp	A/G			intron-variant	ASB11	GRCh38.p7	X:15310632	AAAAACGATTAAACT[A/G]TTTTTGTAATTTTTA	140456
rs768278027	snp	C/T	6.8426e-05	0.00584879	missense	ASB11	GRCh38.p7	X:15289575	AGGGGAGTTCCGAGC[C/T]GAGGCACCTCATGGT	140456
rs768324026	snp	A/G	0.000529661	0.016265	upstream-variant-2KB, intron-variant	ASB11	GRCh38.p7	X:15315123	TTAAAGAAAATAATT[A/G]TATACAAGTAATTAC	140456
rs768456556	snp	A/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15302967	AGCCACTTTCAGGGA[A/G]ACAAGCTACTGAATG	140456
rs768472092	snp	A/G	6.91659e-05	0.00588032	missense	ASB11	GRCh38.p7	X:15288036	GCTGCAGCATGGAGT[A/G]GGGTGTCCAGCCACT	140456
rs768497033	snp	A/G					GRCh38.p7	X:15275514	TATATGCATATGTAT[A/G]TGTATACATGCCTGT	140456
rs768530830	snp	A/G			intron-variant	ASB11	GRCh38.p7	X:15309114	TAGAGACGGGATTTC[A/G]CCATGTTGCCCAGGC	140456
rs768533080	snp	A/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15312864	TTATGGGATAATTTA[A/G]GAATTAGAGAGACTG	140456
rs768553623	in-del	-/TTATTTT	0.00528398	0.051128			GRCh38.p7	X:15276306	AGTGACATAGCAAGC[-/TTATTTT]TTATTTTTTATTTTT	140456
rs768572255	snp	C/T	0.00949095	0.0682305			GRCh38.p7	X:15276477	GCCCGCCAACACGCC[C/T]GGCTAATTTTTTGTA	140456
rs768603701	snp	A/G			intron-variant	ASB11	GRCh38.p7	X:15307886	TCATACTTTCATGAA[A/G]AGTTTCTAAAGTAAC	140456
rs768662465	snp	A/G	0.00158814	0.0281345	intron-variant	ASB11	GRCh38.p7	X:15286440	GGAAGGCTGAGGCGG[A/G]CGGATCACAATGTCA	140456
rs768693790	snp	G/T			intron-variant	ASB11	GRCh38.p7	X:15292552	CACTTGGAAATTAAC[G/T]GACAACACAGGAGTC	140456
rs768708317	snp	A/G	0.00475684	0.0485365	intron-variant	ASB11	GRCh38.p7	X:15289885	AAAAATTAGCTGGGC[A/G]TGGTGGCACACACCC	140456
rs768734882	snp	A/G	0.00422943	0.0457911	upstream-variant-2KB	ASB11	GRCh38.p7	X:15316850	AGCATCAGACTACTC[A/G]CCATGGTAGTTCCAT	140456
rs768769734	snp	G/T	0.00105904	0.0229869	upstream-variant-2KB	ASB11	GRCh38.p7	X:15316265	TACAAAAATTAGCTG[G/T]GCGTGGTGGCAGGTG	140456
rs768812336	snp	A/G	4.62642e-05	0.00480936	synonymous-codon	ASB11	GRCh38.p7	X:15293279	GCCGCTGCAGCAAGC[A/G]TTGAAGAGGGGTGTG	140456
rs768826979	snp	A/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15295480	AGGGAGATGAAAGAA[A/G]TAAGATGACTCTCAG	140456
rs768835494	in-del	-/T	0.00158814	0.0281345	intron-variant	ASB11	GRCh38.p7	X:15291028	TGAATAATTCTTGTC[-/T]TTTTTTTGAAGAACA	140456
rs768900288	snp	A/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15294781	GGTTTCTATATTTTT[A/G]CTAAAAAATATTTGG	140456
rs768998391	snp	A/G	2.27884e-05	0.00337545	missense	ASB11	GRCh38.p7	X:15283570	GGATGGCTTGATGAC[A/G]TGCTCGACCGAGACA	140456
rs769004538	snp	C/G			upstream-variant-2KB	ASB11	GRCh38.p7	X:15317152	TGCCTTCATTCTTGG[C/G]TATGTTCGATTTTGT	140456
rs769054725	snp	G/T	0.00422943	0.0457911			GRCh38.p7	X:15276567	CGTGATCCGCCCGCC[G/T]TGGCCTCCCAAAGTG	140456
rs769073103	snp	A/G	2.31755e-05	0.003404	missense, intron-variant	ASB11	GRCh38.p7	X:15314483	CCCCAGTTAATTGAA[A/G]CATTCTGATGCTTCG	140456
rs769075043	snp	C/T	0.0110639	0.0735497	intron-variant	ASB11	GRCh38.p7	X:15301130	ACCACGCCTGGCTAA[C/T]TTTTGTACTTTTAGT	140456
rs769143946	snp	A/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15305498	CTAAACATGAATGGA[A/G]TCTCTGGGTGAAGAG	140456
rs769160985	snp	A/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15292044	TGTCGAAAAAAAAAA[A/G]AAAAAGAAAGAAAGA	140456
rs769170837	snp	A/G			intron-variant	ASB11	GRCh38.p7	X:15299459	TCTGTCTGGGTTACA[A/G]TAAGGGGTTGTGGAG	140456
rs769173856	snp	C/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15307984	CAGGGCAGGGTATGG[C/G]CTTCTCCAGCCCACC	140456
rs769195936	snp	G/T	0.000529661	0.016265	utr-variant-3-prime	ASB11	GRCh38.p7	X:15282193	GGTCTAGAAAAATTG[G/T]GGGAAAAAAAAACAT	140456
rs769215407	snp	A/G	0.000280371	0.0118367	utr-variant-5-prime, intron-variant	ASB11	GRCh38.p7	X:15314498	GCATTCTGATGCTTC[A/G]TCCTTGGAGGTCTTA	140456
rs769223500	in-del	-/AA	0.484391	0.0869544			GRCh38.p7	X:15278635	AAGATCCCAGATGAC[-/AA]AAAAAAAAAAAAAAA	140456
rs769273405	snp	C/T	2.55813e-05	0.00357631	intron-variant	ASB11	GRCh38.p7	X:15314348	TTTTTTTTTTTTTTG[C/T]AACTAGTCAAAGTAA	140456
rs769340838	snp	A/C	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15300469	GTTTATAAAAGTAGA[A/C]AAATACATTTTTTAA	140456
rs769350925	snp	C/G			upstream-variant-2KB, intron-variant	ASB11	GRCh38.p7	X:15315307	TAAGTGACAATTTTT[C/G]AAACTACCCACTTAA	140456
rs769411915	snp	C/T	4.56397e-05	0.00477679	missense	ASB11	GRCh38.p7	X:15289590	TGAGGCACCTCATGG[C/T]CAATGTTAACATTAT	140456
rs769468974	snp	A/G					GRCh38.p7	X:15278745	CTTTCCTCTTTGATC[A/G]TTCCATGGCTAATGA	140456
rs769523785	snp	C/G	0.00211696	0.0324653	intron-variant	ASB11	GRCh38.p7	X:15284231	CACTCCAGCCTGGGC[C/G]ACAGAGCGAGACTCC	140456
rs769578751	snp	A/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15310371	TTTGGCAGATCGCCC[A/G]TGTCACAGGGCTGCA	140456
rs769592346	snp	C/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15297157	ATTAGCCGGGCGTGG[C/T]GGCGTGTGCCTGTAG	140456
rs769650226	snp	C/T	2.43208e-05	0.00348709	intron-variant	ASB11	GRCh38.p7	X:15293146	CCCATCAATGTTTCA[C/T]ATGCATTGTGGTGGC	140456
rs769652108	snp	C/T	0.00105904	0.0229869	utr-variant-3-prime	ASB11	GRCh38.p7	X:15283349	CTAACCAGGAGTTTC[C/T]ACTCCTCAAGTGTTC	140456
rs769759994	snp	A/G			intron-variant	ASB11	GRCh38.p7	X:15291765	TATATGGCTGAGCAC[A/G]GTGGCTCATGCCTGT	140456
rs769816918	snp	C/T					GRCh38.p7	X:15277143	ATGCACTGAAAATAC[C/T]GAAAAATCTTAACAG	140456
rs769835587	snp	C/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15297841	AAGCCCAGCAGAAGA[C/G]AGTGAAATACTGCAT	140456
rs769897181	snp	A/G	9.36538e-05	0.00684238	synonymous-codon	ASB11	GRCh38.p7	X:15293300	GAGGGGTGTGGCTCC[A/G]TGAACTGTCACTCCA	140456
rs769918701	snp	C/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15288470	GTAAATGATGGGAAA[C/T]AAAAAAGACAAAAAC	140456
rs769937506	snp	A/G	0.0026455	0.0362733	intron-variant	ASB11	GRCh38.p7	X:15285732	ATCCTGGCCAGGCGC[A/G]GTGGCTCACGCCTGA	140456
rs769971312	snp	C/T	0.00158814	0.0281345			GRCh38.p7	X:15276224	CCAAAATTAGAGACG[C/T]TGGATTACATACCTA	140456
rs770018057	snp	C/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15299570	TAAGGTCTGTGTTGA[C/T]GTTAAATTCTGGTCA	140456
rs770107080	snp	A/G			intron-variant	ASB11	GRCh38.p7	X:15290232	CCAAGTAGCACAGTT[A/G]AAATCACTCTCCAGA	140456
rs770168216	snp	C/T			upstream-variant-2KB	ASB11	GRCh38.p7	X:15317298	ATTAGAATGACTGCC[C/T]GGTTAAGAACTGTTT	140456
rs770214211	snp	A/G			synonymous-codon	ASB11	GRCh38.p7	X:15283592	ACCGAGACACTTCCG[A/G]ACACACAGGCGGCAG	140456
rs770238769	in-del	-/A	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15307899	AAGAGTTTCTAAAGT[-/A]ACACAGACTAGCCCT	140456
rs770243434	snp	A/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15286303	CAAAATGGAACTGGT[A/G]AGTGAAATAAGACCC	140456
rs770294715	snp	C/T	0.00105904	0.0229869	intron-variant	ASB11	GRCh38.p7	X:15313688	AAGAGATTTGTATTC[C/T]AGCTCCAGATTAAAT	140456
rs770361870	snp	A/T			intron-variant	ASB11	GRCh38.p7	X:15296079	AAAAATACAAAAATT[A/T]CTGCACTAAAAATAC	140456
rs770403508	snp	C/T	2.28337e-05	0.0033788	missense	ASB11	GRCh38.p7	X:15283629	GAAAGAGCAGGTGGG[C/T]CTGAGAGAGAAATAA	140456
rs770406180	snp	C/G	2.27931e-05	0.0033758	missense	ASB11	GRCh38.p7	X:15283605	CGGACACACAGGCGG[C/G]AGAGCTGGGAAAGAG	140456
rs770416192	snp	A/G	0.00105904	0.0229869	upstream-variant-2KB	ASB11	GRCh38.p7	X:15316134	TACCTGGCCGGGCGC[A/G]GTGGTTGACTCCTGT	140456
rs770433220	snp	C/T	0.000529661	0.016265			GRCh38.p7	X:15276606	ACAGGCGTGAGCCAC[C/T]GCGCCCAGCCTATTT	140456
rs770455505	snp	C/G					GRCh38.p7	X:15279429	ACATACAGTTTTCCT[C/G]TATTTTGGTTTGCCA	140456
rs770486086	snp	A/C	0.000172951	0.0092976	intron-variant	ASB11	GRCh38.p7	X:15287865	GAAGAGGAATGGATA[A/C]CCAGCCCTTGGTTAC	140456
rs770501484	snp	A/G			intron-variant	ASB11	GRCh38.p7	X:15297276	CCTGGGCGACAGAGT[A/G]AGACTCCGTCTCAAA	140456
rs770568742	in-del	-/AATT			intron-variant	ASB11	GRCh38.p7	X:15290041	ATAAATAAATAAATA[-/AATT]AATTAATTAAATAAC	140456
rs770587509	snp	C/T			intron-variant	ASB11	GRCh38.p7	X:15310264	GGGAGTTTTTCCATT[C/T]CCTTCAGGAAGTATG	140456
rs770681714	snp	A/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15290690	TATCTCCCTAAAAAA[A/T]CATGTCATTACTAAT	140456
rs770746266	snp	C/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15304734	AATACAAAAATTAGG[C/G]TGTGGTGGTGCACGC	140456
rs770784402	snp	C/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15287411	TGCTCATCGCAACCT[C/T]CGCCTCCCAGGTTCA	140456
rs770790537	snp	A/G			intron-variant	ASB11	GRCh38.p7	X:15305112	ACTAACTAGAAAAGG[A/G]ACAGGGATAATTTTA	140456
rs770804405	in-del	-/A	4.64226e-05	0.00481758	upstream-variant-2KB, frameshift-variant	ASB11	GRCh38.p7	X:15315537	ATTAAAAGCTTAAAG[-/A]AAAAAAAACGTAGCA	140456
rs770874074	snp	C/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15288144	CTTCAAATATAGTCA[C/T]TGCATATAAAGACAT	140456
rs770893726	in-del	-/GC	0.00738971	0.0603345			GRCh38.p7	X:15275524	TGTATGTGTATACAT[-/GC]CTGTATATGTATATG	140456
rs770915402	snp	A/G	0.000529661	0.016265			GRCh38.p7	X:15277418	ACAATGTTCTACAGT[A/G]TCTGGCACATAGTAG	140456
rs770960701	snp	A/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15301859	GTCAACCTATTTTAA[A/T]GCTTGTTCTTAAAAT	140456
rs770963434	snp	C/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15305422	AGGGATGACGAAACG[C/T]GCTATCTAAAGGCAA	140456
rs770968202	snp	A/T	2.42615e-05	0.00348284	intron-variant	ASB11	GRCh38.p7	X:15293151	CAATGTTTCACATGC[A/T]TTGTGGTGGCTCATT	140456
rs771029089	snp	A/C	6.91443e-05	0.0058794	intron-variant	ASB11	GRCh38.p7	X:15283660	AAATGGTGTTAACTT[A/C]ATAGTGGTGGGAGGT	140456
rs771052285	snp	A/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15296270	AATAAAAAGATGGAA[A/G]AAAAAAAAACAAAAA	140456
rs771074141	snp	A/C	0.000529661	0.016265			GRCh38.p7	X:15276115	ACTGAAAAAAGATTC[A/C]TGTACAAACCTCATG	140456
rs771116161	snp	A/G	2.34996e-05	0.00342771	intron-variant	ASB11	GRCh38.p7	X:15302709	TAAGCATGAAGGATC[A/G]AGTCTTCAGTTCACT	140456
rs771140251	snp	C/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15309141	AGGCTGGTCTTGAAC[C/T]CCTGACCTCAAGTGA	140456
rs771144950	snp	C/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15285633	TGGTATTTCCAAGCT[C/G]GGATCTGCTGAGGAA	140456
rs771153168	snp	C/T	0.00105904	0.0229869	intron-variant	ASB11	GRCh38.p7	X:15306548	TCTCTACTAAAAATA[C/T]AAAAATTAGCCTGGC	140456
rs771240204	in-del	-/TG			intron-variant	ASB11	GRCh38.p7	X:15305335	TGATAAGGAGGAAAC[-/TG]TGCACCAACCCAAAC	140456
rs771321653	snp	C/T					GRCh38.p7	X:15275393	CCACAACTTACAAAT[C/T]GTTCATTTTTTTAAT	140456
rs771323374	snp	A/G			intron-variant	ASB11	GRCh38.p7	X:15287413	CTCATCGCAACCTCC[A/G]CCTCCCAGGTTCAAG	140456
rs771345251	snp	A/G	0.00475684	0.0485365	upstream-variant-2KB, intron-variant	ASB11	GRCh38.p7	X:15315202	ACCTATTTACTTCTT[A/G]AATAACAACTGCTAC	140456
rs771372708	snp	G/T	0.000529661	0.016265			GRCh38.p7	X:15278915	ATGAACCTATATTAT[G/T]CTTATTGGTTTGTAA	140456
rs771435987	snp	C/T	2.28441e-05	0.00337957	missense	ASB11	GRCh38.p7	X:15288009	TGGATGACCTCCACA[C/T]TGGACTGCCTCGCTG	140456
rs771480136	snp	C/T			utr-variant-3-prime	ASB11	GRCh38.p7	X:15281910	ACCATAGTGGCCAGG[C/T]GGTTCTCGAACTCCT	140456
rs771504225	snp	A/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15290003	CACTCCAGCCTGGCC[A/G]ACAAAGCGAGACTCT	140456
rs771506712	snp	C/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15284057	GGAGATGGAGACCAT[C/T]CTGGCTAACACGGTG	140456
rs771540181	snp	A/T			intron-variant	ASB11	GRCh38.p7	X:15299263	GGGTAGTCAGGGCAC[A/T]GCCTAGTTTTATACA	140456
rs771594039	snp	A/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15290462	TACCTATGAGAAAGA[A/G]TAAAGAAGTCTTAAG	140456
rs771659173	snp	A/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15312130	TCTCTCCTGAGAAAG[A/T]GCCTGCAGAAATATC	140456
rs771682124	snp	C/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15298079	CTTATGACATGGGTC[C/T]CTCTTCTCCCAGAGC	140456
rs771690353	snp	A/G	2.40419e-05	0.00346704	missense	ASB11	GRCh38.p7	X:15287890	GGTTACCTTCACGGA[A/G]CAAGAGTGCCTGCTC	140456
rs771701231	snp	A/G			intron-variant	ASB11	GRCh38.p7	X:15307531	TCTAATGCCACCACT[A/G]ATCTGACAGAAGGCG	140456
rs771773967	snp	G/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15299391	AGATTATAGACAGAT[G/T]GAAAATTTTTCTGAT	140456
rs771877384	in-del	-/T	0.022522	0.1037			GRCh38.p7	X:15276573	CCGCCCGCCGTGGCC[-/T]CCCAAAGTGCTGGGA	140456
rs771879437	in-del	-/C			intron-variant	ASB11	GRCh38.p7	X:15308223	ACACTGGGGCTTACA[-/C]CCCATGTACCTTTTC	140456
rs771886491	snp	A/G	2.30963e-05	0.00339818	upstream-variant-2KB, missense	ASB11	GRCh38.p7	X:15315526	AAAAAAACTTTAATT[A/G]AAAGCTTAAAGAAAA	140456
rs771926873	snp	A/G			intron-variant	ASB11	GRCh38.p7	X:15290419	TTGGATATATGGCCT[A/G]CAACAGTACTTTGGT	140456
rs771955355	snp	C/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15304621	GGCCAGGCTCACGCC[C/T]GTAATCCCAGCACTT	140456
rs771968580	snp	C/T	0.000529661	0.016265			GRCh38.p7	X:15276507	ATTTTTTAGTAGAGA[C/T]GGGGTTTCACCGTGT	140456
rs772039757	snp	C/G	0.0173306	0.0914601	intron-variant	ASB11	GRCh38.p7	X:15284122	CCGGGTGTGGTGGCG[C/G]GTGCCTATAGTCCCA	140456
rs772045096	in-del	-/C	2.41782e-05	0.00347686	frameshift-variant	ASB11	GRCh38.p7	X:15287886	CCTTGGTTACCTTCA[-/C]GGAGCAAGAGTGCCT	140456
rs772084604	snp	C/T	0.00105904	0.0229869	utr-variant-3-prime	ASB11	GRCh38.p7	X:15282465	ATCCACAGAAAAAAA[C/T]ATTGACCCAGCATTG	140456
rs772108325	snp	C/T			intron-variant	ASB11	GRCh38.p7	X:15306640	CCCGGGAGGTGGAGG[C/T]TGCAGTGAGCCAAGA	140456
rs772149642	snp	A/G	0.00105904	0.0229869	intron-variant	ASB11	GRCh38.p7	X:15303884	AACAGCCTTAGAGCC[A/G]CCTTCCAGACATATT	140456
rs772152625	snp	A/G	2.27884e-05	0.00337545	missense	ASB11	GRCh38.p7	X:15283539	CGTTCGAGTGGCTCT[A/G]GCAGATGTAGCTTGT	140456
rs772168441	snp	C/T			intron-variant	ASB11	GRCh38.p7	X:15304572	AAAATACAAGATGGG[C/T]CTTAAACATCTTCCA	140456
rs772195892	snp	C/T	0.00105904	0.0229869	intron-variant	ASB11	GRCh38.p7	X:15308245	TACCTTTTCTACCCA[C/T]TGGCATTTGGCCACC	140456
rs772253027	snp	A/G	0.00105904	0.0229869	intron-variant	ASB11	GRCh38.p7	X:15287363	ACGGAGTCTCGCTCT[A/G]TCACCCAGGCTGGAA	140456
rs772277335	in-del	-/TTTT	0.00230017	0.0338348	intron-variant	ASB11	GRCh38.p7	X:15314330	TATCAGAAGCATTAC[-/TTTT]TTTTTTTTTTTTTGT	140456
rs772448156	snp	A/G	2.28102e-05	0.00337707	utr-variant-3-prime	ASB11	GRCh38.p7	X:15283465	GTACAGCAGACAACA[A/G]TCTGTGTCATTCCAA	140456
rs772509897	snp	A/G			intron-variant	ASB11	GRCh38.p7	X:15312988	AGTATTTTGTGGGGC[A/G]GGGGAAGATTTGTAA	140456
rs772514051	in-del	-/A	0.265183	0.249539	intron-variant	ASB11	GRCh38.p7	X:15296267	AAAATAAAAAGATGG[-/A]AAAAAAAAAAAACAA	140456
rs772515454	snp	C/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15301616	AAGCCAGATGATTGC[C/G]TAGTTGTGGAAGAAA	140456
rs772564808	snp	A/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15312233	TTAAACTTTAAAAAA[A/G]AAAAAAAAATATACA	140456
rs772623378	in-del	-/TATGTGTATACATTTGTATATGCATATG	0.0026455	0.0362733			GRCh38.p7	X:15275482	ATTTATATATGTATA[-/TATGTGTATACATTTGTATATGCATATG]TATGTGTATACATTT	140456
rs772743413	snp	C/T	2.3541e-05	0.00343074	utr-variant-5-prime, intron-variant	ASB11	GRCh38.p7	X:15314520	GAGGTCTTATTTCTT[C/T]AGATAAGACTGCTGT	140456
rs772747984	snp	C/T			intron-variant	ASB11	GRCh38.p7	X:15294966	AAGACAATTGCCTCT[C/T]CTTGAGTGGGCTGAA	140456
rs772760293	snp	C/T	0.00317376	0.039709	intron-variant	ASB11	GRCh38.p7	X:15284059	AGATGGAGACCATCC[C/T]GGCTAACACGGTGAA	140456
rs772767246	snp	C/T	0.0026455	0.0362733	intron-variant	ASB11	GRCh38.p7	X:15292120	GACTTACATGATGTT[C/T]GGGAAATGACTAACA	140456
rs772797326	snp	A/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15289354	CTGAGAAATACAGAC[A/G]CTCATTTCTCTAGAG	140456
rs772820473	snp	A/C	2.27889e-05	0.00337549	missense	ASB11	GRCh38.p7	X:15283578	TGATGACATGCTCGA[A/C]CGAGACACTTCCGGA	140456
rs772872848	snp	A/C			intron-variant	ASB11	GRCh38.p7	X:15310130	TTCCAGAAACTGCCA[A/C]AGTGGGGTCTCCTGC	140456
rs772885150	snp	C/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15284001	CTCACGCCTGTAATC[C/G]CAGCACTTTGGGAGG	140456
rs772919113	snp	A/G	4.55866e-05	0.00477402	missense	ASB11	GRCh38.p7	X:15283606	GGACACACAGGCGGC[A/G]GAGCTGGGAAAGAGC	140456
rs772924035	snp	A/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15286538	GGTGTGGTGGTGCAC[A/G]CCTGTAGTCCCAGCT	140456
rs772940413	in-del	-/T	2.28266e-05	0.00337828	frameshift-variant	ASB11	GRCh38.p7	X:15288002	AGCAGGTGGATGACC[-/T]TCCACATTGGACTGC	140456
rs773007519	snp	C/T					GRCh38.p7	X:15277310	TTTTTCTTTTTATCA[C/T]TTCCTGATATGATAT	140456
rs773049573	snp	A/C	0.000529661	0.016265	upstream-variant-2KB	ASB11	GRCh38.p7	X:15317048	TATTTCATGAATCAA[A/C]CTTCTCTAGTTGGGC	140456
rs773121309	snp	A/G			intron-variant	ASB11	GRCh38.p7	X:15296017	GAGGCCAAGGCGGGC[A/G]GATCACCTGAGGTCA	140456
rs773169424	snp	C/T	0.000529661	0.016265			GRCh38.p7	X:15276518	GAGACGGGGTTTCAC[C/T]GTGTTAGCCAGGATG	140456
rs773219546	snp	C/T	0.00475684	0.0485365	intron-variant	ASB11	GRCh38.p7	X:15303925	TTGCTTATCTGCAAA[C/T]AAGACTAACTAGTTT	140456
rs773254084	in-del	-/ACAG	0.00475684	0.0485365	intron-variant	ASB11	GRCh38.p7	X:15309056	CGAGTAGCTGGGACT[-/ACAG]ACACACATCACCACT	140456
rs773295245	snp	G/T					GRCh38.p7	X:15275252	CTATCATGGGCTTTT[G/T]GCCTTAACATTGACT	140456
rs773296332	snp	C/T	0.000529661	0.016265	utr-variant-3-prime	ASB11	GRCh38.p7	X:15281720	TTTTTTGTTTTGAGA[C/T]GGAGTCTCGCTCTGT	140456
rs773390640	snp	A/G			upstream-variant-2KB	ASB11	GRCh38.p7	X:15317412	TAAAGACCTTGAGTC[A/G]TCTTAACTCTCAAGG	140456
rs773417355	snp	C/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15308260	TTGGCATTTGGCCAC[C/T]TCTCCTAGTGTCTGT	140456
rs773505120	snp	A/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15300496	TTAACAGTGTATAAG[A/G]GTAAAGAAGTAGGGG	140456
rs773554026	snp	A/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15313854	CAGGAGTTCAAGACC[A/G]GCCTGGCCAACATGG	140456
rs773605325	in-del	-/TTTTT	0.00115141	0.0239662	intron-variant	ASB11	GRCh38.p7	X:15314330	TATCAGAAGCATTAC[-/TTTTT]TTTTTTTTTTTTGTA	140456
rs773632768	snp	A/G	0.0026455	0.0362733	intron-variant	ASB11	GRCh38.p7	X:15305704	TAATAACAAAGAAAA[A/G]CAGATAAAAAATTTT	140456
rs773636633	snp	C/T	2.36047e-05	0.00343537	missense	ASB11	GRCh38.p7	X:15293311	CTCCGTGAACTGTCA[C/T]TCCATTGACCTAATG	140456
rs773735630	in-del	-/AAAAC			intron-variant	ASB11	GRCh38.p7	X:15297290	TGAGACTCCGTCTCA[-/AAAAC]AAAACAAAACAAAAC	140456
rs773764041	snp	C/T	0.00105904	0.0229869	intron-variant	ASB11	GRCh38.p7	X:15285144	ATTTAATCTTTCTTT[C/T]TTTTTTTTTTTTTTT	140456
rs773800709	snp	A/C	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15292256	AAATTGGCAAGTGAC[A/C]TGTTTAATAACCTGG	140456
rs773871027	snp	A/G	7.23493e-05	0.0060141	missense	ASB11	GRCh38.p7	X:15287887	CTTGGTTACCTTCAC[A/G]GAGCAAGAGTGCCTG	140456
rs773872197	snp	A/C/G/T	0.000205122	0.0101255	missense	ASB11	GRCh38.p7	X:15283603	TCCGGACACACAGGC[A/C/G/T]GCAGAGCTGGGAAAG	140456
rs773872500	snp	A/G			intron-variant	ASB11	GRCh38.p7	X:15295188	GCTGGGACTACAGGC[A/G]CGTGCCACCATGCCT	140456
rs773886828	snp	A/C	3.29462e-05	0.00405857	intron-variant	ASB11	GRCh38.p7	X:15283639	GTGGGCCTGAGAGAG[A/C]AATAAAAATGGTGTT	140456
rs773890792	snp	C/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15284373	AACAGAGGGACAATA[C/T]GGAAAGGGTGTCAGC	140456
rs773903395	snp	C/G	0.0026455	0.0362733	intron-variant	ASB11	GRCh38.p7	X:15288684	AGGTCAGGAGTTCGA[C/G]ACCAGCCTGGCCAAC	140456
rs773954903	snp	A/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15289234	GCTCTTTCTTGCTGC[A/G]TATGGATAAGGAGGG	140456
rs774016287	in-del	-/A	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15298070	TCTTCAAAACTTATG[-/A]CATGGGTCTCTCTTC	140456
rs774050040	snp	C/T			intron-variant	ASB11	GRCh38.p7	X:15312960	GTTTTGAATAAAGAG[C/T]TGTTATTTTTTAAGT	140456
rs774065680	snp	C/G	0.00105904	0.0229869	intron-variant	ASB11	GRCh38.p7	X:15310576	TCAATAACATTGGTT[C/G]AGATGGAGTACAGCT	140456
rs774066559	snp	C/T			intron-variant	ASB11	GRCh38.p7	X:15296114	ATTAGCTGGACGTGG[C/T]GGCGGGCACCTGTAA	140456
rs774113059	snp	C/T	0.000529661	0.016265			GRCh38.p7	X:15278851	GACTATTTATTTGTA[C/T]GTTATTTGATAAGTT	140456
rs774162977	snp	C/T	0.00105904	0.0229869	intron-variant	ASB11	GRCh38.p7	X:15284054	TCAGGAGATGGAGAC[C/T]ATCCTGGCTAACACG	140456
rs774202192	snp	G/T	2.51389e-05	0.00354525	upstream-variant-2KB, intron-variant	ASB11	GRCh38.p7	X:15315384	GAATTATCTAGGAGG[G/T]ATTTTCTTTAAATAT	140456
rs774227746	in-del	-/T	0.000534331	0.0163365			GRCh38.p7	X:15276492	GGCTAATTTTTTGTA[-/T]TTTTTTAGTAGAGAC	140456
rs774241608	snp	C/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15303827	AAGTGCTCCGGACAT[C/T]GTATGATTAATAAGT	140456
rs774273600	snp	C/T	0.000529661	0.016265	upstream-variant-2KB	ASB11	GRCh38.p7	X:15316892	TCCCATGGCAAGGTT[C/T]CCTCCTGATCATTCA	140456
rs774328119	snp	A/G			intron-variant	ASB11	GRCh38.p7	X:15306566	AAATTAGCCTGGCAC[A/G]GTGGTAGGCGCCTGT	140456
rs774330290	snp	A/C			missense	ASB11	GRCh38.p7	X:15289569	ACATATAGGGGAGTT[A/C]CGAGCTGAGGCACCT	140456
rs774365012	snp	C/T	0.00475684	0.0485365	intron-variant	ASB11	GRCh38.p7	X:15311883	CAAAATGTTTGACTG[C/T]GGGAGGCAGCTCCAG	140456
rs774365256	snp	A/G	2.36088e-05	0.00343568	intron-variant	ASB11	GRCh38.p7	X:15288077	GACACTGGCTCCTTA[A/G]CAAAACAGATGGCCA	140456
rs774454578	snp	A/G			intron-variant	ASB11	GRCh38.p7	X:15305127	AACAGGGATAATTTT[A/G]TAGAACAGAATTGTA	140456
rs774464638	snp	G/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15307348	CTTTTTGCCACCAAG[G/T]ACTGGTTTCATGGAA	140456
rs774490290	snp	C/T			upstream-variant-2KB	ASB11	GRCh38.p7	X:15317566	AAGTAGGCAATCATT[C/T]AGTCATGTCAGACCA	140456
rs774541045	snp	A/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15285825	CCTAGCCAACATGAT[A/G]AAACCCCATCTCTAC	140456
rs774579877	snp	A/G			intron-variant	ASB11	GRCh38.p7	X:15300017	TTTCATGTCCTGAAT[A/G]TGACATCATTACTCT	140456
rs774582451	in-del	-/A			intron-variant	ASB11	GRCh38.p7	X:15284252	GCGAGACTCCGCCTC[-/A]AAAAAAAAAAAAAAA	140456
rs774594896	snp	C/T	0.00211696	0.0324653	upstream-variant-2KB	ASB11	GRCh38.p7	X:15316338	CTTGAACCTGGGAGG[C/T]GGAGGTTGCAGTGAG	140456
rs774636589	snp	C/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15299645	TTCAACCCCCCTTTC[C/G]TGTCATGGCCTGAAC	140456
rs774663775	snp	A/G	2.4154e-05	0.00347511	missense	ASB11	GRCh38.p7	X:15297606	ATAAGGCTTTGGCAC[A/G]GGCCACGTGACCTCC	140456
rs774694024	snp	G/T					GRCh38.p7	X:15275470	TGTGCACATGTGCAT[G/T]TATATATGTATATAT	140456
rs774726252	snp	C/T			intron-variant	ASB11	GRCh38.p7	X:15287490	AGCCACCACATCTGG[C/T]TAATTTCTGTATTTT	140456
rs774759657	snp	A/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15313780	CTTGAGGCCGGGCGC[A/G]GTGGCTCACGCCTGT	140456
rs774825686	snp	C/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15284170	GGCAGGAGAATGGCG[C/T]GAACCCGGGAGGCGG	140456
rs774829192	snp	A/C			intron-variant	ASB11	GRCh38.p7	X:15302885	TGCCCACCCACTGTG[A/C]GAGGAGGTTTGGGGG	140456
rs774834037	snp	G/T	2.34307e-05	0.00342269	intron-variant	ASB11	GRCh38.p7	X:15302712	GCATGAAGGATCAAG[G/T]CTTCAGTTCACTTAC	140456
rs774902326	snp	A/G	0.00105904	0.0229869	intron-variant	ASB11	GRCh38.p7	X:15292046	TCGAAAAAAAAAAAA[A/G]AAAGAAAGAAAGACA	140456
rs774941074	snp	A/T	0.00105904	0.0229869	intron-variant	ASB11	GRCh38.p7	X:15300479	GTAGACAAATACATT[A/T]TTTAACAGTGTATAA	140456
rs774997800	snp	C/T	0.00105904	0.0229869	intron-variant	ASB11	GRCh38.p7	X:15284238	GCCTGGGCGACAGAG[C/T]GAGACTCCGCCTCAA	140456
rs775024383	in-del	-/AAAG	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15296473	AACAAAATTAGAAAC[-/AAAG]AACATCTGGCAACTA	140456
rs775025199	snp	A/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15291183	ATTCTGTGGATATTT[A/G]TCCTTAACATGCTTT	140456
rs775030870	snp	A/G	0.000529661	0.016265			GRCh38.p7	X:15277625	TGAAGGGTTAATTTG[A/G]TCAGGTCTGTCCGCC	140456
rs775054234	snp	A/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15304835	AGCTAAGATTATGCC[A/T]CTGTACTCTGGCCTG	140456
rs775060087	in-del	-/TT	0.239914	0.249796	intron-variant	ASB11	GRCh38.p7	X:15314330	TATCAGAAGCATTAC[-/TT]TTTTTTTTTTTTTTT	140456
rs775128998	snp	A/G	0.00633741	0.0559334	intron-variant	ASB11	GRCh38.p7	X:15310404	CACATTATGAAGATA[A/G]TTTACTCTACAAATA	140456
rs775130448	snp	C/T	2.36141e-05	0.00343606	synonymous-codon, splice-acceptor-variant	ASB11	GRCh38.p7	X:15297631	ACCTCCAAGGCATGC[C/T]TCGTGGAGAGAAGAC	140456
rs775131592	in-del	-/G	4.75585e-05	0.00487616	frameshift-variant	ASB11	GRCh38.p7	X:15297624	CCACGTGACCTCCAA[-/G]GCATGCCTCGTGGAG	140456
rs775137827	snp	A/G	4.58363e-05	0.00478707	missense	ASB11	GRCh38.p7	X:15288021	ACATTGGACTGCCTC[A/G]CTGCAGCATGGAGTG	140456
rs775201678	snp	A/G			intron-variant	ASB11	GRCh38.p7	X:15297503	GTAAGCCATCTGGAA[A/G]GTAAACTATCATTAA	140456
rs775210782	snp	C/G	0.0026455	0.0362733	intron-variant	ASB11	GRCh38.p7	X:15302125	ATCTCATGACACAGC[C/G]CTGTGGAGAGGCTCA	140456
rs775260894	in-del	-/AACA	0.0100156	0.0700533			GRCh38.p7	X:15278824	CAATTTTCCATCTTT[-/AACA]AACATTCTTATGACT	140456
rs775290731	snp	C/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15289090	TGTTAGTTTCAGTTC[C/T]CGTGTTTCCAGTGAA	140456
rs775320558	snp	C/T	9.47721e-05	0.0068831	synonymous-codon	ASB11	GRCh38.p7	X:15287906	CAAGAGTGCCTGCTC[C/T]ACGCTGCTTTTTGGA	140456
rs775387534	snp	C/T			intron-variant	ASB11	GRCh38.p7	X:15292478	TCAGTGGCATCTTCT[C/T]GGTTCAGGTCTAGTC	140456
rs775462023	snp	C/G	0.00422943	0.0457911	intron-variant	ASB11	GRCh38.p7	X:15309414	AGATGGGACCATCTA[C/G]TTGCAGGAAAACAAG	140456
rs775484374	snp	G/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15288549	CTTTATGTCAGGGGC[G/T]AAGTTTGTTGAATCT	140456
rs775594547	snp	C/T	0.00581083	0.0535878	intron-variant	ASB11	GRCh38.p7	X:15285741	AGGCGCGGTGGCTCA[C/T]GCCTGAAATCCCTGC	140456
rs775629062	snp	C/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15293725	CTGGTCTACTATAAT[C/T]CATGCAAATTACACA	140456
rs775675180	snp	C/T	2.28102e-05	0.00337707	utr-variant-3-prime	ASB11	GRCh38.p7	X:15283473	GACAACAATCTGTGT[C/T]ATTCCAAGTATCTTC	140456
rs775688249	snp	C/T			intron-variant	ASB11	GRCh38.p7	X:15301741	CTTACCAGGCCCCTA[C/T]TCATTTTTCAAGGTG	140456
rs775769528	snp	G/T	2.42239e-05	0.00348014	intron-variant	ASB11	GRCh38.p7	X:15293156	TTTCACATGCATTGT[G/T]GTGGCTCATTTACCT	140456
rs775873392	snp	A/T	2.31227e-05	0.00340012	intron-variant	ASB11	GRCh38.p7	X:15302725	AGTCTTCAGTTCACT[A/T]ACTTGTGCAATTAAA	140456
rs775962264	snp	G/T			intron-variant	ASB11	GRCh38.p7	X:15289076	GTAAACCACCCTCTT[G/T]TTAGTTTCAGTTCTC	140456
rs775982955	snp	C/G	6.83628e-05	0.00584609	missense	ASB11	GRCh38.p7	X:15283550	CTCTGGCAGATGTAG[C/G]TTGTGGATGGCTTGA	140456
rs776035305	snp	C/T	0.00105904	0.0229869	intron-variant	ASB11	GRCh38.p7	X:15300404	ATGTTTTACTCATAT[C/T]GGTTTAATGTTTTAC	140456
rs776043230	snp	C/T			upstream-variant-2KB, intron-variant	ASB11	GRCh38.p7	X:15315096	TTCATTGTTAAAGTT[C/T]GCTTTAAAATATTAA	140456
rs776075218	snp	C/T	0.000529661	0.016265	downstream-variant-500B	ASB11	GRCh38.p7	X:15281521	TATGTATTTTACACT[C/T]ACAACACATCTTAAT	140456
rs776078024	snp	C/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15307227	TAGACTCAAGTCATA[C/T]ACACAACATGGATAA	140456
rs776141286	in-del	-/AAC/AACAAC/AACAACAAC	0.0913156	0.196776	intron-variant	ASB11	GRCh38.p7	X:15306703	TGACACTTTGTCTCA[-/AAC/AACAAC/AACAACAAC]AACAACAACAACAAC	140456
rs776167931	snp	C/T			intron-variant	ASB11	GRCh38.p7	X:15313073	TGAAAAATACTGGTC[C/T]AGGCATGTTACTGCC	140456
rs776267958	snp	A/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15284160	GGGAGGCTGAGGCAG[A/G]AGAATGGCGTGAACC	140456
rs776275606	snp	A/G	0.00105904	0.0229869	intron-variant	ASB11	GRCh38.p7	X:15304744	TTAGGGTGTGGTGGT[A/G]CACGCCTGTAGTGCC	140456
rs776292530	snp	C/T			intron-variant	ASB11	GRCh38.p7	X:15306871	TCAGACATGTTACGC[C/T]CTTGCCTAGTTGCTC	140456
rs776349360	snp	A/C	2.37691e-05	0.00344731	splice-donor-variant, intron-variant	ASB11	GRCh38.p7	X:15314367	TAGTCAAAGTAACAT[A/C]CCTCCCTGAAATGTG	140456
rs776350890	snp	A/G	2.2811e-05	0.00337713	missense	ASB11	GRCh38.p7	X:15289578	GGAGTTCCGAGCTGA[A/G]GCACCTCATGGTCAA	140456
rs776424749	snp	C/G			intron-variant	ASB11	GRCh38.p7	X:15292615	TTTGGAAAGTTGCAG[C/G]CTTTTCTTTTCAATA	140456
rs776441670	in-del	-/CATTCTCACCATCTC	2.43674e-05	0.00349043	intron-variant	ASB11	GRCh38.p7	X:15293360	AAGGATTTGTTATTT[-/CATTCTCACCATCTC]CATTCTCACCATCTC	140456
rs776443970	snp	C/T					GRCh38.p7	X:15277063	GTTTATGGGAAAAGC[C/T]GGAATCATAGATACT	140456
rs776446968	snp	C/G					GRCh38.p7	X:15275621	ACATACATAGAGAAG[C/G]AAATGTAGCAAAATG	140456
rs776458541	snp	C/T	0.000210067	0.0102464	missense	ASB11	GRCh38.p7	X:15288042	GCATGGAGTGGGGTG[C/T]CCAGCCACTGGCCAT	140456
rs776509711	snp	A/T	0.000529661	0.016265			GRCh38.p7	X:15276217	ATGTGAACCAAAATT[A/T]GAGACGTTGGATTAC	140456
rs776531591	in-del	-/C	0.000232342	0.0107758	upstream-variant-2KB, frameshift-variant	ASB11	GRCh38.p7	X:15315546	CTTAAAGAAAAAAAA[-/C]GTAGCAAACATTGTA	140456
rs776544561	snp	A/G	2.32964e-05	0.00341287	missense	ASB11	GRCh38.p7	X:15293290	AAGCATTGAAGAGGG[A/G]TGTGGCTCCGTGAAC	140456
rs776580239	snp	C/T	0.000529661	0.016265	upstream-variant-2KB	ASB11	GRCh38.p7	X:15317211	GCCAAAATATAGTTA[C/T]ACAAGTGGCCTAATA	140456
rs776615453	snp	C/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15288159	TTGCATATAAAGACA[C/T]TTTAAGTACCATGAC	140456
rs776616184	snp	C/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15293431	ACGCTGGTGAATAAG[C/T]GAGGGAACTCCACAT	140456
rs776654333	snp	A/C/G	0.00105918	0.022993	intron-variant	ASB11	GRCh38.p7	X:15296288	AAAAAAACAAAAAAA[A/C/G]AAAATGCACGACCAC	140456
rs776728636	snp	A/C			intron-variant	ASB11	GRCh38.p7	X:15289458	GAAGCTGTAGAAAAT[A/C]AACAAAGTTAACAGG	140456
rs776741645	snp	A/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15287470	TAGCTGGAACTACAG[A/G]CGCCAGCCACCACAT	140456
rs776764799	snp	C/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15310234	AAATTGAGGATAAAA[C/G]TTACTTGGCAGCTTG	140456
rs776771097	snp	A/G	0.00475684	0.0485365	intron-variant	ASB11	GRCh38.p7	X:15301259	TGAGCCACCACATCC[A/G]GCCAGTCCACCTTTT	140456
rs776929594	snp	A/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15307096	TGGCAACTTGCAATT[A/T]AAAGAGTTAACATAG	140456
rs776934683	snp	C/T	0.00738971	0.0603345			GRCh38.p7	X:15275526	TATGTGTATACATGC[C/T]TGTATATGTATATGT	140456
rs776934705	snp	C/T	2.39481e-05	0.00346027	synonymous-codon	ASB11	GRCh38.p7	X:15293174	GGCTCATTTACCTCT[C/T]TTCACTGCCTCATGG	140456
rs776934708	snp	C/T	0.00158814	0.0281345	intron-variant	ASB11	GRCh38.p7	X:15292500	GGTCTAGTCTGTACA[C/T]ACAGTCTTTAAATTC	140456
rs776990875	snp	C/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15285186	TCACTCGGTCGCCCA[C/G]GCTGAAATGCAGTGG	140456
rs777023812	snp	C/T			upstream-variant-2KB	ASB11	GRCh38.p7	X:15317205	AGACAAGCCAAAATA[C/T]AGTTATACAAGTGGC	140456
rs777087383	snp	C/T	0.000529661	0.016265			GRCh38.p7	X:15280295	GTAAGCAAGAACATA[C/T]GGTGTTTATCTTTCT	140456
rs777120840	snp	A/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15298209	GGCTTGGGGAGTAAG[A/G]AAAACCTTGCAAATG	140456
rs777175264	snp	G/T			intron-variant	ASB11	GRCh38.p7	X:15299525	AGCAGGCTTCAGAGA[G/T]AATAGATTGTAAATG	140456
rs777175281	snp	A/G			utr-variant-3-prime	ASB11	GRCh38.p7	X:15282164	GGCAAAATTGTCTCC[A/G]GTTGAGAGCCAAAGG	140456
rs777195031	snp	A/G	0.00211696	0.0324653	intron-variant	ASB11	GRCh38.p7	X:15300934	AGGTGGGTGCAAGAC[A/G]TTTCATTGTGCACCT	140456
rs777236701	snp	A/T	0.000529661	0.016265	upstream-variant-2KB, intron-variant	ASB11	GRCh38.p7	X:15315325	ACTACCCACTTAAAA[A/T]CAAAGTATAAATATA	140456
rs777272933	snp	G/T			intron-variant	ASB11	GRCh38.p7	X:15304353	GTTCTGAAAATGGGG[G/T]AAACTTGAATGCACT	140456
rs777308199	snp	C/T	0.000529661	0.016265			GRCh38.p7	X:15278936	TGGTTTGTAAATGAA[C/T]TCTTTATATGTTGAA	140456
rs777326093	in-del	-/CTTGTT	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15308723	GACTTTAGAACACAC[-/CTTGTT]CTGGTTTTAAGAACT	140456
rs777389243	snp	A/G	3.29636e-05	0.00405964	intron-variant	ASB11	GRCh38.p7	X:15293147	CCATCAATGTTTCAC[A/G]TGCATTGTGGTGGCT	140456
rs777429763	snp	G/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15307789	AATTTCTTGCTCTTA[G/T]GTGCTGGTTCCTGAC	140456
rs777450735	snp	A/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15286948	CACAAATAATCAATA[A/T]AGGCTCCGAAAATAT	140456
rs777464833	snp	A/G			intron-variant	ASB11	GRCh38.p7	X:15287295	CAGGACAGAAATGGA[A/G]ATTCAAGATTTTCGG	140456
rs777496544	snp	A/T			intron-variant	ASB11	GRCh38.p7	X:15298638	TGTAAGACCAAAGCA[A/T]GGAGAGCCACAGAGA	140456
rs777498938	snp	A/G			downstream-variant-500B	ASB11	GRCh38.p7	X:15281351	TGGCTAGTAGCTACC[A/G]TATTGAATAGCACAG	140456
rs777502717	snp	A/G	0	0	intron-variant	ASB11	GRCh38.p7	X:15284823	GAAAACCTAATTACT[A/G]GTCTACACAAAGTTT	140456
rs777516021	snp	A/G	0.00475684	0.0485365	intron-variant	ASB11	GRCh38.p7	X:15300244	AGATCATCTAGAGTG[A/G]ATCACCTCAATTGTG	140456
rs777557288	snp	G/T	0.00105904	0.0229869			GRCh38.p7	X:15277381	ATGAGTTTTTTGGAA[G/T]CAAACAGCATGTCTG	140456
rs777561847	snp	A/G	2.43229e-05	0.00348724	intron-variant	ASB11	GRCh38.p7	X:15293357	CCCAAAGGATTTGTT[A/G]TTTCATTCTCACCAT	140456
rs777624898	snp	C/T	0.00158814	0.0281345	utr-variant-3-prime	ASB11	GRCh38.p7	X:15281928	TTCTCGAACTCCTGA[C/T]AGTGCGATCTGCCTG	140456
rs777692960	snp	C/T			intron-variant	ASB11	GRCh38.p7	X:15297109	CCATCCTGGCTAACA[C/T]AGTGAAACTCTGTCT	140456
rs777699355	snp	C/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15284210	TGAGCCGAGATCGGG[C/T]CACTGCACTCCAGCC	140456
rs777753362	snp	C/G	4.63623e-05	0.00481446	missense, intron-variant	ASB11	GRCh38.p7	X:15314484	CCCAGTTAATTGAAG[C/G]ATTCTGATGCTTCGT	140456
rs777775669	in-del	-/A	4.61515e-05	0.0048035	upstream-variant-2KB, frameshift-variant	ASB11	GRCh38.p7	X:15315510	TGGGTTAGGAGAGCC[-/A]AAAAAAACTTTAATT	140456
rs777786866	snp	A/G	2.37296e-05	0.00344445	intron-variant	ASB11	GRCh38.p7	X:15302701	TTATAGCATAAGCAT[A/G]AAGGATCAAGTCTTC	140456
rs777861666	snp	C/T	0.00475684	0.0485365	intron-variant	ASB11	GRCh38.p7	X:15288902	AAAAAAAAAAAGATA[C/T]TTCATTTTTCCACGG	140456
rs777876813	snp	C/T	4.6092e-05	0.0048004	intron-variant	ASB11	GRCh38.p7	X:15302816	CAGCAATCTGAAACA[C/T]AAATCAAGCTCAAAG	140456
rs777894017	snp	A/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15310024	TTCCCAACTGGAAAC[A/G]AAGTAACTCTCAAGA	140456
rs778056389	snp	G/T	0.00791544	0.0624105	upstream-variant-2KB, intron-variant	ASB11	GRCh38.p7	X:15315143	CAAGTAATTACTTTG[G/T]CTAGTAGAAATGAAG	140456
rs778072299	snp	C/T	0.000529661	0.016265			GRCh38.p7	X:15276402	GCTCACTGCAAGCTC[C/T]GCCTCCCGAGTTCAC	140456
rs778131132	snp	C/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15297019	TGGTACAAGGCCGGG[C/T]GCGGTGGCTCACGCC	140456
rs778149127	snp	A/G			intron-variant	ASB11	GRCh38.p7	X:15308948	TTGAGATGGAGTCTC[A/G]CTCTGTCCCCTAGGC	140456
rs778159255	snp	A/C			intron-variant	ASB11	GRCh38.p7	X:15302594	GCAGTGAGGTATGAG[A/C]GGACATACGTGCCTC	140456
rs778177113	snp	C/T	0.00105904	0.0229869	intron-variant	ASB11	GRCh38.p7	X:15302665	CTGCTACAGCCAAAG[C/T]TAATAAAGAATGATG	140456
rs778192709	snp	C/T	0.0026455	0.0362733	intron-variant	ASB11	GRCh38.p7	X:15310935	GAGGTTGCAGTGAGC[C/T]GAGATCACATCACTG	140456
rs778231280	snp	A/G	4.56277e-05	0.00477617	synonymous-codon	ASB11	GRCh38.p7	X:15287984	GTTAGCTCCATAGTC[A/G]GTTAGCAGGTGGATG	140456
rs778285698	snp	A/C	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15301626	ATTGCCTAGTTGTGG[A/C]AGAAAGACATGATGG	140456
rs778328303	snp	C/T	0.00158814	0.0281345	intron-variant	ASB11	GRCh38.p7	X:15307624	CAGGCCATGGACTGG[C/T]ACTGGTCTGTGGCCT	140456
rs778334178	snp	G/T	4.57064e-05	0.00478029	synonymous-codon	ASB11	GRCh38.p7	X:15288011	GATGACCTCCACATT[G/T]GACTGCCTCGCTGCA	140456
rs778404186	snp	A/T					GRCh38.p7	X:15277954	TGCTAATGCCACTAT[A/T]TTGGGTTTATATGTC	140456
rs778405956	snp	C/T			intron-variant	ASB11	GRCh38.p7	X:15289795	TTGGGAGGCTGAGAC[C/T]GGCGGATTCCCTGAG	140456
rs778425250	snp	A/C	3.29576e-05	0.00405928	intron-variant	ASB11	GRCh38.p7	X:15287867	AGAGGAATGGATACC[A/C]AGCCCTTGGTTACCT	140456
rs778446774	snp	C/G			upstream-variant-2KB, intron-variant	ASB11	GRCh38.p7	X:15314921	CTACCATATAAAATG[C/G]GTTTAGTGAAGAGCT	140456
rs778527395	snp	C/T	0.000529661	0.016265			GRCh38.p7	X:15281191	ACAAAAGCAAAACTT[C/T]GTCTCAAAAAAGAAA	140456
rs778626933	snp	C/T	0.00158814	0.0281345	intron-variant	ASB11	GRCh38.p7	X:15295128	GCTCACTGCAACCTC[C/T]GCCTCCTGGGTTCAA	140456
rs778651435	snp	A/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15307048	TTGAAGGTACTGTAA[A/G]TATTCCATTTAAAAA	140456
rs778706298	snp	C/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15289947	GAGAATCACTTGAAC[C/T]GGGGAGGAGGAGGTT	140456
rs778723266	snp	A/G	0.0157677	0.0873799			GRCh38.p7	X:15284115	AAATTAGCCGGGTGT[A/G]GTGGCGGGTGCCTAT	140456
rs778723704	snp	A/G	0.00158814	0.0281345			GRCh38.p7	X:15286001	CAAGAGCAAAACTCC[A/G]TCTAAAATAATAATA	140456
rs778810047	in-del	-/A	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15300158	GCAGAAGTGTGCTAG[-/A]AAAAAACTGTTACGG	140456
rs778889998	snp	C/T			utr-variant-3-prime	ASB11	GRCh38.p7	X:15283213	GGTACAAGAAGATCC[C/T]GAATCATCAAAAAAC	140456
rs778890631	snp	C/T			intron-variant	ASB11	GRCh38.p7	X:15299208	TAAGTGACCAATGGC[C/T]TGTGACAAGCTCTCA	140456
rs778918010	snp	C/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15313595	GACCTTAGAATACTA[C/T]GCTACTTGCAAATTA	140456
rs778945511	snp	C/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15304594	CATCTTCCAAGAAAG[C/T]AAGAAAGTGCTGGCC	140456
rs779003157	snp	C/G	4.5871e-05	0.00478888	missense, intron-variant	ASB11	GRCh38.p7	X:15314457	TGAAACTTCACAATT[C/G]TTCTCATTTTCCCCA	140456
rs779004266	snp	A/G	4.55783e-05	0.00477358	missense	ASB11	GRCh38.p7	X:15283593	CCGAGACACTTCCGG[A/G]CACACAGGCGGCAGA	140456
rs779006595	snp	G/T	2.34461e-05	0.00342381	intron-variant	ASB11	GRCh38.p7	X:15302847	TCAAGGCCTGGAGAC[G/T]TCTTCCTGTAACTTG	140456
rs779016321	snp	C/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15287308	GAAATTCAAGATTTT[C/T]GGGGTATAAACAAGG	140456
rs779028107	in-del	-/AG			intron-variant	ASB11	GRCh38.p7	X:15307885	ATCATACTTTCATGA[-/AG]AGTTTCTAAAGTAAC	140456
rs779037323	snp	C/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15296202	TGCAGTGAGCTGAGA[C/T]TGTGCCACTGCACTC	140456
rs779039959	in-del	-/AAC			intron-variant	ASB11	GRCh38.p7	X:15306706	CACTTTGTCTCAAAC[-/AAC]AACAACAACAACAAC	140456
rs779051817	in-del	-/T	0.000529661	0.016265			GRCh38.p7	X:15277259	TCAGCTTATCTAAAA[-/T]AGTAAGCCTCTTTCA	140456
rs779076518	snp	C/T	0.000529661	0.016265			GRCh38.p7	X:15275463	GGGTGTGTGTGCACA[C/T]GTGCATTTATATATG	140456
rs779099363	snp	A/C	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15296879	TGGGTATATACCCAG[A/C]AGAAAGGAAAACAGT	140456
rs779180078	snp	C/T			intron-variant	ASB11	GRCh38.p7	X:15311264	GTTAGACACAATTAA[C/T]TATGTTGCAGTGTAT	140456
rs779190033	snp	C/T	0.00422943	0.0457911			GRCh38.p7	X:15276568	GTGATCCGCCCGCCG[C/T]GGCCTCCCAAAGTGC	140456
rs779290235	snp	A/G			intron-variant	ASB11	GRCh38.p7	X:15288933	ACTCTTGGTTTCTGT[A/G]TATGCCTTTTAGAAT	140456
rs779310499	snp	A/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15305280	GAAGAACACACCACC[A/G]CTTCTGTGATATTTC	140456
rs779319818	snp	A/G	0.00158814	0.0281345	intron-variant	ASB11	GRCh38.p7	X:15309878	GAGGCTGAGGCAGGA[A/G]AATGGTGTGAACCCG	140456
rs779389617	snp	C/G			utr-variant-3-prime	ASB11	GRCh38.p7	X:15283467	ACAGCAGACAACAAT[C/G]TGTGTCATTCCAAGT	140456
rs779409414	snp	C/T	0.00158814	0.0281345	utr-variant-3-prime	ASB11	GRCh38.p7	X:15282987	ATATACGTATATATA[C/T]ATACGTATATGTATG	140456
rs779417872	snp	A/C	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15308971	CCCTAGGCTGGAGTG[A/C]AGTGGTGCAATCTCA	140456
rs779501036	snp	A/G	2.28081e-05	0.00337691	synonymous-codon	ASB11	GRCh38.p7	X:15289562	GCAGGCCACATATAG[A/G]GGAGTTCCGAGCTGA	140456
rs779554951	snp	A/G	0.00105904	0.0229869			GRCh38.p7	X:15278664	AAAAAAAATGCACTC[A/G]CGAGAACACTTTGAA	140456
rs779590974	snp	C/T	0.000343348	0.0130979	intron-variant	ASB11	GRCh38.p7	X:15290010	GCCTGGCCGACAAAG[C/T]GAGACTCTGTCTCAA	140456
rs779593224	snp	A/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15301168	GGGTTTCACCATGTT[A/G]CCCAGGCTGGTCTCG	140456
rs779667491	snp	A/G			intron-variant	ASB11	GRCh38.p7	X:15300859	ATTAAAAATATACCA[A/G]TGAAAGTATTGAGGT	140456
rs779705576	snp	C/T	0.000529661	0.016265	upstream-variant-2KB, intron-variant	ASB11	GRCh38.p7	X:15314897	ACTTTGTTTGGAGTG[C/T]TTTGCATGCTACCAT	140456
rs779750193	snp	A/T			intron-variant	ASB11	GRCh38.p7	X:15309055	CCGAGTAGCTGGGAC[A/T]ACAGACACACATCAC	140456
rs779764212	snp	C/G	0.00105904	0.0229869	intron-variant	ASB11	GRCh38.p7	X:15284972	AGAAAGCTACCTGGA[C/G]GACCAAACAATCGAT	140456
rs779841394	snp	A/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15293035	GAAGTTACTGCTGTG[A/G]GATTTCTAGGCCACA	140456
rs779845204	snp	C/T			upstream-variant-2KB	ASB11	GRCh38.p7	X:15317119	TTATTTTTAGTTTTC[C/T]TCATCACTCTAGGTC	140456
rs779847802	snp	A/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15289840	ACCAGCCTGGCCAAC[A/G]TGGTGAAACCCCATC	140456
rs779863672	snp	A/G			intron-variant	ASB11	GRCh38.p7	X:15299302	AAACATGAGACATCA[A/G]TCAAATACATGTAAA	140456
rs779952990	snp	A/G	0.00105904	0.0229869	intron-variant	ASB11	GRCh38.p7	X:15306869	CTTCAGACATGTTAC[A/G]CTCTTGCCTAGTTGC	140456
rs779968694	snp	A/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15311727	TGTAAAGTTCCTCCA[A/G]TTCTGAAAACCAAGC	140456
rs780043959	snp	A/C	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15298888	AGAGGTCTCTGAAGT[A/C]CTAGAGTCCGGGGCC	140456
rs780084318	snp	A/C/G	0.0570788	0.159001	intron-variant	ASB11	GRCh38.p7	X:15312835	CTTGATTTTTAATAC[A/C/G]CCTAAATATATTGTT	140456
rs780113143	snp	A/G					GRCh38.p7	X:15278530	CCATGGTCTGCAGTT[A/G]CAGTGGGCAATGGAA	140456
rs780134919	snp	A/G	2.35275e-05	0.00342975	intron-variant	ASB11	GRCh38.p7	X:15283679	GTGGTGGGAGGTGGG[A/G]TGGAAGGGGGAAATC	140456
rs780137576	snp	C/T	0.00105904	0.0229869	intron-variant	ASB11	GRCh38.p7	X:15290325	TATTACTCTGAAAAG[C/T]TAGTGCTCAAACCCA	140456
rs780236914	snp	C/T	0.000529661	0.016265	utr-variant-3-prime	ASB11	GRCh38.p7	X:15281947	GCGATCTGCCTGCCT[C/T]GGCCTCCCAAAATGC	140456
rs780298820	snp	A/G			intron-variant	ASB11	GRCh38.p7	X:15296887	TACCCAGAAGAAAGG[A/G]AAACAGTATATCCAA	140456
rs780339174	snp	C/T	2.29822e-05	0.00338977	missense, intron-variant	ASB11	GRCh38.p7	X:15314462	CTTCACAATTCTTCT[C/T]ATTTTCCCCAGTTAA	140456
rs780346268	snp	A/G			intron-variant	ASB11	GRCh38.p7	X:15290882	TGAATTACAGCATCA[A/G]TATGTCAAGGTATTG	140456
rs780354160	snp	C/T	0.0026455	0.0362733	intron-variant	ASB11	GRCh38.p7	X:15287695	GTAAATGCCCTTTGG[C/T]TGTTAGTGAATATAC	140456
rs780386657	snp	C/T					GRCh38.p7	X:15280833	ATTCTTATACACTAT[C/T]GGTGGGAATGTAAAT	140456
rs780410634	snp	A/T			intron-variant	ASB11	GRCh38.p7	X:15306076	TGGCCTCCAGCTCCA[A/T]CCATGTCTCTGCAAA	140456
rs780425517	snp	G/T	7.64468e-05	0.00618203	intron-variant	ASB11	GRCh38.p7	X:15314339	CATTACTTTTTTTTT[G/T]TTTTTTTGTAACTAG	140456
rs780440644	snp	A/G	0.00105904	0.0229869	intron-variant	ASB11	GRCh38.p7	X:15284095	GTGTCCACTAAAAAT[A/G]CAAAAAATTAGCCGG	140456
rs780477344	snp	A/G	0.00211696	0.0324653			GRCh38.p7	X:15276466	GGACTACAGGCGCCC[A/G]CCAACACGCCTGGCT	140456
rs780514857	snp	A/G	2.31182e-05	0.00339979	synonymous-codon	ASB11	GRCh38.p7	X:15293215	CCAGGTGCACCTCCA[A/G]CTGGGCCTTGGCTCC	140456
rs780530253	snp	A/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15286354	AGATTCAGGGTTGGG[A/G]CCTTATGACATTAAG	140456
rs780534057	snp	A/G	0.00370173	0.0428621	intron-variant	ASB11	GRCh38.p7	X:15296110	AAAAATTAGCTGGAC[A/G]TGGTGGCGGGCACCT	140456
rs780637481	in-del	-/T/TT/TTT	0.538135	0.124407	intron-variant	ASB11	GRCh38.p7	X:15314329	TATCAGAAGCATTAC[-/T/TT/TTT]TTTTTTTTTTTTTTT	140456
rs780703213	snp	C/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15284218	GATCGGGCCACTGCA[C/G]TCCAGCCTGGGCGAC	140456
rs780802582	snp	A/G			intron-variant	ASB11	GRCh38.p7	X:15287235	TCAGATTGTCTCCCA[A/G]TATTACAAAGCAGAG	140456
rs780809010	snp	C/T			intron-variant	ASB11	GRCh38.p7	X:15295684	AACTTTCTCTTATTT[C/T]GTTTCTCATTCTGAT	140456
rs780871030	snp	A/G	0.000529661	0.016265	utr-variant-3-prime	ASB11	GRCh38.p7	X:15282976	TGTGTGTATATATAT[A/G]CGTATATATATATAC	140456
rs780901580	snp	A/G	0.00158814	0.0281345	intron-variant	ASB11	GRCh38.p7	X:15291896	AAAAATTAGCCAATT[A/G]TGGTGGCGGGCACCT	140456
rs780929809	snp	C/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15305456	ACCTGATCCTTTTGC[C/T]ATAAAGGACATTATT	140456
rs780942277	snp	C/T	0.000529661	0.016265			GRCh38.p7	X:15275381	GGATCATGATGCCCA[C/T]AACTTACAAATCGTT	140456
rs780976350	snp	C/T			intron-variant	ASB11	GRCh38.p7	X:15301024	TGGAGTGAAGTGACG[C/T]GATCTCGGTTCACTG	140456
rs780992710	snp	A/G			intron-variant	ASB11	GRCh38.p7	X:15285275	CCTCCCGGGTAGGTG[A/G]GATTACAGGCGGGTG	140456
rs780994674	snp	C/T			intron-variant	ASB11	GRCh38.p7	X:15302281	CCAGAATCACCTAGC[C/T]AAGCTGCTCCCTGGC	140456
rs780996377	in-del	-/GACAGAGAGAGAG	0.00791544	0.0624105	intron-variant	ASB11	GRCh38.p7	X:15301526	AGACAGAGAGAGAGA[-/GACAGAGAGAGAG]AGAGAAAGAAAAAGA	140456
rs781053483	snp	C/T	0.000529661	0.016265	upstream-variant-2KB, intron-variant	ASB11	GRCh38.p7	X:15314773	TACTTTTGTAGCATC[C/T]CACCACAATTAAAGT	140456
rs781159153	snp	C/G	0.000529661	0.016265			GRCh38.p7	X:15278520	TTTGTGGCATCCATG[C/G]TCTGCAGTTGCAGTG	140456
rs781263178	snp	A/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15298671	TCACTATGAGTCTAG[A/G]AACAGGCTGGCATGG	140456
rs781289457	snp	A/C			intron-variant	ASB11	GRCh38.p7	X:15290154	AAAAAGAGGAGCATG[A/C]CCATGCTTCCCCACT	140456
rs781292147	snp	C/T	2.30484e-05	0.00339465	missense	ASB11	GRCh38.p7	X:15302729	TTCAGTTCACTTACT[C/T]GTGCAATTAAAGTTT	140456
rs781293837	snp	A/G	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15312516	AGCTTCCAAAAAAAA[A/G]AAAAAAAAAGAGTGC	140456
rs781365395	snp	C/G			utr-variant-3-prime	ASB11	GRCh38.p7	X:15282622	GGGACACCCAGTGTT[C/G]TCAATCCTAGAACTG	140456
rs781393399	snp	A/G	3.31312e-05	0.00406995	intron-variant	ASB11	GRCh38.p7	X:15297551	TGGCCAGACAGACCC[A/G]AGTGGGCAGGGGCAG	140456
rs781410649	snp	C/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15311202	GTTAAAATAAATATT[C/T]TCCAGAATGTCCAGT	140456
rs781564627	snp	C/T	0.000205386	0.0101317	missense	ASB11	GRCh38.p7	X:15287961	CCCTGAGCATTTCTA[C/T]GCTTCAGGTTAGCTC	140456
rs781592954	snp	C/T	0.00158814	0.0281345			GRCh38.p7	X:15276559	CCTGACCTCGTGATC[C/T]GCCCGCCGTGGCCTC	140456
rs781652574	snp	C/T	0.000529661	0.016265	intron-variant	ASB11	GRCh38.p7	X:15303431	AGCCATCCTGGGCCA[C/T]GAGTTGGACAAGCTT	140456
rs781653107	snp	C/T	0.000371299	0.0136203	upstream-variant-2KB, missense	ASB11	GRCh38.p7	X:15315485	TTCTATTTCCTTTGA[C/T]GATATAGAAATGGGT	140456
rs781671376	snp	A/G	0.000529661	0.016265	upstream-variant-2KB	ASB11	GRCh38.p7	X:15316113	GACCAGTTAAAAAAG[A/G]CCATTTACCTGGCCG	140456
rs781716812	snp	A/C	0.0026455	0.0362733			GRCh38.p7	X:15276427	GTTCACGCCATTCTC[A/C]TGCCTCAGCCTCCCG	140456
rs781726059	snp	C/T	2.49414e-05	0.0035313	intron-variant	ASB11	GRCh38.p7	X:15287844	AGGGGAGAGAATGTG[C/T]TTATGGAAGAGGAAT	140456
rs796418984	snp	A/T					GRCh38.p7	X:15277835	GGCCAGCTCCTGTCC[A/T]GTTCAAACCAGTTAA	140456
rs796551191	snp	C/T			intron-variant	ASB11	GRCh38.p7	X:15313817	AGCACTTTGCGAGGC[C/T]GAGGCGGGCGGATCA	140456

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