Item | Value |
---|---|
geneid | 6884 |
ensemblid | ENSG00000197780.11 |
hgncid | 11546 |
symbol | TAF13 |
name | TATA-box binding protein associated factor 13 |
refseq_nuc | NM_005645.4 |
refseq_prot | NP_005636.1 |
ensembl_nuc | ENST00000338366.6 |
ensembl_prot | ENSP00000355051.4 |
mane_status | MANE Select |
chr | chr1 |
start | 109064140 |
end | 109076003 |
strand | - |
ver | v1.2 |
region | chr1:109064140-109076003 |
region5000 | chr1:109059140-109081003 |
regionname0 | TAF13_chr1_109064140_109076003 |
regionname5000 | TAF13_chr1_109059140_109081003 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 372 | 410 | 98 | 74 | 176 | 14 | 46 | TAF13_chr1_109059140_109081003 | TAF13 | ATGGC others(367): Show |
chr1 | 109059140 | 109081003 | ||
a0001c0002 | 0/0 | 372 | 4 | 0 | 0 | 4 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | ATGGC others(367): Show |
chr1 | 109059140 | 109081003 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 817 | 181 | 21 | 38 | 89 | 7 | 26 | TAF13_chr1_109059140_109081003 | TAF13 | AGTGT others(812): Show |
chr1 | 109059140 | 109081003 |
a0001c0001t0002 | 0/1 | 818 | 111 | 20 | 17 | 60 | 4 | 9 | TAF13_chr1_109059140_109081003 | TAF13 | AGTGT others(813): Show |
chr1 | 109059140 | 109081003 |
a0001c0001t0003 | 0/0 | 819 | 37 | 7 | 4 | 23 | 0 | 3 | TAF13_chr1_109059140_109081003 | TAF13 | AGTGT others(814): Show |
chr1 | 109059140 | 109081003 |
a0001c0001t0004 | 0/0 | 816 | 21 | 15 | 4 | 1 | 1 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | AGTGT others(811): Show |
chr1 | 109059140 | 109081003 |
a0001c0001t0005 | 1/0 | 814 | 14 | 13 | 0 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | AGTGT others(809): Show |
chr1 | 109059140 | 109081003 |
a0001c0001t0006 | 0/0 | 820 | 13 | 6 | 1 | 3 | 0 | 3 | TAF13_chr1_109059140_109081003 | TAF13 | AGTGT others(815): Show |
chr1 | 109059140 | 109081003 |
a0001c0001t0007 | 0/0 | 815 | 9 | 7 | 0 | 0 | 1 | 1 | TAF13_chr1_109059140_109081003 | TAF13 | AGTGT others(810): Show |
chr1 | 109059140 | 109081003 |
a0001c0001t0008 | 0/0 | 814 | 8 | 4 | 3 | 0 | 0 | 1 | TAF13_chr1_109059140_109081003 | TAF13 | AGTGT others(809): Show |
chr1 | 109059140 | 109081003 |
a0001c0001t0009 | 0/0 | 804 | 5 | 1 | 1 | 0 | 0 | 3 | TAF13_chr1_109059140_109081003 | TAF13 | AGTGT others(799): Show |
chr1 | 109059140 | 109081003 |
a0001c0001t0010 | 0/0 | 818 | 3 | 1 | 2 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | AGTGT others(813): Show |
chr1 | 109059140 | 109081003 |
a0001c0001t0011 | 0/0 | 819 | 3 | 0 | 3 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | AGTGT others(814): Show |
chr1 | 109059140 | 109081003 |
a0001c0001t0012 | 0/0 | 815 | 2 | 2 | 0 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | AGTGT others(810): Show |
chr1 | 109059140 | 109081003 |
a0001c0001t0013 | 0/0 | 816 | 1 | 0 | 1 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | AGTGT others(811): Show |
chr1 | 109059140 | 109081003 |
a0001c0001t0014 | 0/0 | 794 | 1 | 1 | 0 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | AGTGT others(789): Show |
chr1 | 109059140 | 109081003 |
a0001c0001t0015 | 0/0 | 818 | 1 | 0 | 0 | 0 | 1 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | AGTGT others(813): Show |
chr1 | 109059140 | 109081003 |
a0001c0002t0002 | 0/0 | 818 | 3 | 0 | 0 | 3 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | AGTGT others(813): Show |
chr1 | 109059140 | 109081003 |
a0001c0002t0003 | 0/0 | 819 | 1 | 0 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | AGTGT others(814): Show |
chr1 | 109059140 | 109081003 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 70 | 3 | 23 | 33 | 2 | 9 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0004 | 0/0 | 11 | 3 | 1 | 6 | 0 | 1 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0007 | 0/0 | 7 | 0 | 1 | 3 | 1 | 2 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0008 | 0/0 | 6 | 1 | 0 | 5 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0010 | 0/0 | 5 | 2 | 1 | 1 | 0 | 1 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0012 | 0/0 | 4 | 2 | 1 | 0 | 1 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0015 | 0/0 | 4 | 1 | 1 | 2 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0046 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0051 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0053 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0055 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0056 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0057 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0002g0002 | 0/0 | 24 | 0 | 2 | 18 | 2 | 2 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0002g0003 | 0/0 | 13 | 5 | 1 | 6 | 0 | 1 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0002g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0002g0019 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0002g0020 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0002g0026 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0002g0029 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0002g0035 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0002g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0002g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0002g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0002g0045 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0002g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0002g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0002g0052 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0002g0164 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0003g0006 | 0/0 | 9 | 0 | 1 | 6 | 0 | 2 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0003g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0003g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0003g0028 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0003g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0003g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0004g0009 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0004g0025 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0004g0050 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0004g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0004g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0004g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0004g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0004g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0005g0005 | 1/0 | 10 | 9 | 0 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0005g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0005g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0005g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0005g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0006g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0006g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0006g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0006g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0006g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0006g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0006g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0006g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0006g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0006g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0007g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0007g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0007g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0007g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0007g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0007g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0008g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0008g0024 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0008g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0008g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0009g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0009g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0009g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0009g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0010g0039 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0010g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0011g0017 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0012g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0012g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0013g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0014g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0001t0015g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0002t0002g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
a0001c0002t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0007 | g0129 | EUR | GBR | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | GBR | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0029 | EUR | GBR | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG00280 | hp1 | a0001 | c0001 | t0004 | g0071 | EUR | FIN | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0060 | EUR | FIN | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG00408 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | CHS | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG00544 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | CHS | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG00597 | hp2 | a0001 | c0001 | t0006 | g0116 | EAS | CHS | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | CHS | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | CHS | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG00639 | hp2 | a0001 | c0001 | t0004 | g0025 | AMR | PUR | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG00642 | hp1 | a0001 | c0001 | t0004 | g0149 | AMR | PUR | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0028 | AMR | PUR | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0035 | AMR | PUR | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0102 | AMR | PUR | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG00738 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0115 | AMR | PUR | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01070 | hp1 | a0001 | c0001 | t0004 | g0050 | AMR | PUR | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0038 | AMR | PUR | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0038 | AMR | PUR | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01099 | hp2 | a0001 | c0001 | t0009 | g0031 | AMR | PUR | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01109 | hp1 | a0001 | c0001 | t0008 | g0141 | AMR | PUR | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01109 | hp2 | a0001 | c0001 | t0006 | g0170 | AMR | PUR | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01167 | hp1 | a0001 | c0001 | t0008 | g0024 | AMR | PUR | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01167 | hp2 | a0001 | c0001 | t0013 | g0058 | AMR | PUR | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01169 | hp1 | a0001 | c0001 | t0008 | g0024 | AMR | PUR | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0045 | AMR | PUR | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0190 | AMR | CLM | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01261 | hp1 | a0001 | c0001 | t0010 | g0086 | AMR | CLM | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0029 | AMR | CLM | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0047 | AMR | CLM | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | CLM | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0068 | AMR | CLM | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01433 | hp2 | a0001 | c0001 | t0004 | g0009 | AMR | CLM | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01516 | hp1 | a0001 | c0001 | t0015 | g0108 | EUR | IBS | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0065 | EUR | IBS | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | IBS | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01884 | hp1 | a0001 | c0001 | t0010 | g0039 | AFR | ACB | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01891 | hp1 | a0001 | c0001 | t0006 | g0144 | AFR | ACB | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01891 | hp2 | a0001 | c0001 | t0007 | g0044 | AFR | ACB | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01928 | hp1 | a0001 | c0001 | t0011 | g0017 | AMR | PEL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01928 | hp2 | a0001 | c0001 | t0011 | g0017 | AMR | PEL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01952 | hp1 | a0001 | c0001 | t0011 | g0017 | AMR | PEL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0178 | AMR | PEL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01978 | hp2 | a0001 | c0001 | t0003 | g0157 | AMR | PEL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | KHV | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0156 | AFR | ACB | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0045 | AFR | ACB | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | KHV | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0125 | AFR | ACB | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0052 | AFR | ACB | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CDX | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02155 | hp2 | a0001 | c0001 | t0004 | g0130 | EAS | CDX | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CDX | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | ACB | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02257 | hp2 | a0001 | c0001 | t0012 | g0140 | AFR | ACB | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02258 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | ACB | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02273 | hp2 | a0001 | c0001 | t0010 | g0039 | AMR | PEL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0169 | AFR | ACB | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02280 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | ACB | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | PEL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02451 | hp1 | a0001 | c0001 | t0005 | g0005 | AFR | ACB | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0186 | AFR | ACB | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | KHV | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | KHV | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02572 | hp2 | a0001 | c0001 | t0007 | g0152 | AFR | GWD | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02615 | hp2 | a0001 | c0001 | t0006 | g0030 | AFR | GWD | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0123 | AFR | GWD | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02647 | hp1 | a0001 | c0001 | t0005 | g0005 | AFR | GWD | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02647 | hp2 | a0001 | c0001 | t0007 | g0018 | AFR | GWD | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02683 | hp2 | a0001 | c0001 | t0008 | g0024 | SAS | PJL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0107 | SAS | PJL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02717 | hp1 | a0001 | c0001 | t0005 | g0005 | AFR | GWD | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02717 | hp2 | a0001 | c0001 | t0012 | g0147 | AFR | GWD | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02723 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | GWD | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0028 | AFR | GWD | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02735 | hp2 | a0001 | c0001 | t0003 | g0006 | SAS | PJL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02809 | hp1 | a0001 | c0001 | t0007 | g0018 | AFR | GWD | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02818 | hp1 | a0001 | c0001 | t0004 | g0075 | AFR | GWD | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02818 | hp2 | a0001 | c0001 | t0004 | g0025 | AFR | GWD | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02886 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | GWD | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02886 | hp2 | a0001 | c0001 | t0008 | g0139 | AFR | GWD | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0089 | AFR | GWD | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02895 | hp2 | a0001 | c0001 | t0005 | g0091 | AFR | GWD | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02896 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | GWD | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02896 | hp2 | a0001 | c0001 | t0004 | g0009 | AFR | GWD | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02897 | hp1 | a0001 | c0001 | t0007 | g0100 | AFR | GWD | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02897 | hp2 | a0001 | c0001 | t0004 | g0148 | AFR | GWD | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02922 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | ESN | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02922 | hp2 | a0001 | c0001 | t0008 | g0023 | AFR | ESN | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ESN | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02970 | hp1 | a0001 | c0001 | t0004 | g0025 | AFR | ESN | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ESN | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02976 | hp1 | a0001 | c0001 | t0005 | g0005 | AFR | ESN | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG03017 | hp1 | a0001 | c0001 | t0007 | g0132 | SAS | PJL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0064 | AFR | GWD | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG03098 | hp1 | a0001 | c0001 | t0005 | g0151 | AFR | MSL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG03098 | hp2 | a0001 | c0001 | t0004 | g0126 | AFR | MSL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG03130 | hp1 | a0001 | c0001 | t0005 | g0005 | AFR | ESN | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG03130 | hp2 | a0001 | c0001 | t0004 | g0063 | AFR | ESN | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG03139 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | ESN | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG03195 | hp1 | a0001 | c0001 | t0005 | g0005 | AFR | ESN | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG03195 | hp2 | a0001 | c0001 | t0008 | g0023 | AFR | ESN | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG03209 | hp1 | a0001 | c0001 | t0005 | g0005 | AFR | MSL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG03209 | hp2 | a0001 | c0001 | t0009 | g0090 | AFR | MSL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG03225 | hp1 | a0001 | c0001 | t0006 | g0097 | AFR | MSL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG03225 | hp2 | a0001 | c0001 | t0005 | g0150 | AFR | MSL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | MSL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | MSL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0085 | AFR | MSL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG03490 | hp2 | a0001 | c0001 | t0006 | g0037 | SAS | PJL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0019 | SAS | PJL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0026 | SAS | PJL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG03492 | hp1 | a0001 | c0001 | t0006 | g0120 | SAS | PJL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0019 | SAS | PJL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG03516 | hp1 | a0001 | c0001 | t0004 | g0088 | AFR | ESN | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG03516 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | ESN | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG03540 | hp1 | a0001 | c0001 | t0014 | g0131 | AFR | GWD | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG03579 | hp1 | a0001 | c0001 | t0005 | g0142 | AFR | MSL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | STU | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG03704 | hp1 | a0001 | c0001 | t0006 | g0037 | SAS | PJL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG03704 | hp2 | a0001 | c0001 | t0003 | g0006 | SAS | PJL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG03710 | hp2 | a0001 | c0001 | t0009 | g0062 | SAS | PJL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | BEB | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG03834 | hp2 | a0001 | c0001 | t0009 | g0031 | SAS | BEB | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0173 | SAS | BEB | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0019 | SAS | STU | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | STU | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | STU | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0026 | SAS | STU | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | STU | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG04228 | hp1 | a0001 | c0001 | t0009 | g0061 | SAS | STU | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18522 | hp1 | a0001 | c0001 | t0006 | g0098 | AFR | YRI | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0059 | AFR | YRI | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | CHB | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18747 | hp2 | a0001 | c0002 | t0002 | g0021 | EAS | CHB | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18906 | hp1 | a0001 | c0001 | t0004 | g0093 | AFR | YRI | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0121 | AFR | YRI | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18940 | hp1 | a0001 | c0001 | t0003 | g0136 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18944 | hp1 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18947 | hp2 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18948 | hp2 | a0001 | c0001 | t0003 | g0117 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18952 | hp1 | a0001 | c0001 | t0003 | g0118 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18956 | hp2 | a0001 | c0001 | t0006 | g0040 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18962 | hp1 | a0001 | c0001 | t0003 | g0145 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18963 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18965 | hp1 | a0001 | c0002 | t0003 | g0111 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18967 | hp2 | a0001 | c0001 | t0003 | g0146 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18972 | hp1 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18977 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18989 | hp2 | a0001 | c0001 | t0006 | g0040 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18995 | hp2 | a0001 | c0002 | t0002 | g0021 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18997 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18998 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19001 | hp2 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19010 | hp2 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19030 | hp1 | a0001 | c0001 | t0006 | g0030 | AFR | LWK | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19030 | hp2 | a0001 | c0001 | t0007 | g0018 | AFR | LWK | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19043 | hp2 | a0001 | c0001 | t0006 | g0143 | AFR | LWK | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19067 | hp2 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19074 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19077 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19086 | hp2 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19088 | hp1 | a0001 | c0002 | t0002 | g0021 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19088 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19089 | hp2 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19240 | hp1 | a0001 | c0001 | t0007 | g0044 | AFR | YRI | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA19240 | hp2 | a0001 | c0001 | t0008 | g0023 | AFR | YRI | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ASW | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ASW | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | TSI | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0029 | EUR | TSI | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0165 | EUR | TSI | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | TSI | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0124 | AFR | ACB | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02486 | hp1 | a0001 | c0001 | t0003 | g0099 | AFR | ACB | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | ACB | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | MSL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | MSL | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG06807 | hp1 | a0001 | c0001 | t0004 | g0128 | AFR | USA | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
HG06807 | hp2 | a0001 | c0001 | t0004 | g0050 | AFR | USA | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18955 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0185 | AFR | USA | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0164 | REF | REF | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
homoSapiens | grch38p0 | a0001 | c0001 | t0005 | g0005 | REF | REF | TAF13_chr1_109059140_109081003 | TAF13 | chr1 | 109059140 | 109081003 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:109064577 | A | G | 1 | a0001c0002 | 4 | NA18747.hp2 NA18965.hp1 NA18995.hp2 others(1): Show |
synonymous_variant | LOW | c.321T>C | p.Asn107Asn | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 4/4 | 377/814 | 321/375 | 107/124 | chr1 | 109064577 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:109064156 | C | CA | 2 | a0001c0001t0007 a0001c0001t0012 |
11 | HG00099.hp1 HG01891.hp2 HG02257.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*366dupT | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 4/4 | 366 | chr1 | 109064156 | ||||||
chr1:109064156 | C | CAA | 2 | a0001c0001t0004 a0001c0001t0013 |
22 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*365_*366dupTT | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 4/4 | 366 | chr1 | 109064156 | ||||||
chr1:109064156 | C | CAAA | 1 | a0001c0001t0001 | 181 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(178): Show |
3_prime_UTR_variant | MODIFIER | c.*364_*366dupTTT | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 4/4 | 366 | chr1 | 109064156 | ||||||
chr1:109064156 | C | CAAAA | 4 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0015 others(1): Show |
117 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*363_*366dupTTTT | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 4/4 | 366 | chr1 | 109064156 | ||||||
chr1:109064156 | C | CAAAAA | 3 | a0001c0001t0003 a0001c0001t0011 a0001c0002t0003 |
41 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*362_*366dupTTTTT | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 4/4 | 366 | chr1 | 109064156 | ||||||
chr1:109064156 | C | CAAAAAA | 1 | a0001c0001t0006 | 13 | HG00597.hp2 HG01109.hp2 HG01891.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*361_*366dupTTTTTT | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 4/4 | 366 | chr1 | 109064156 | ||||||
chr1:109064156 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0009 | 5 | HG01099.hp2 HG03209.hp2 HG03710.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*357_*366delTTTTTT others(4): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 4/4 | 357 | chr1 | 109064156 | ||||||
chr1:109064156 | CAAAAAAA others(13): Show |
C | 1 | a0001c0001t0014 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*347_*366delTTTTTT others(14): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 4/4 | 347 | chr1 | 109064156 | ||||||
chr1:109064303 | C | T | 2 | a0001c0001t0010 a0001c0001t0011 |
6 | HG01261.hp1 HG01884.hp1 HG01928.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*220G>A | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 4/4 | 220 | chr1 | 109064303 | ||||||
chr1:109064373 | T | G | 2 | a0001c0001t0008 a0001c0001t0012 |
10 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*150A>C | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 4/4 | 150 | chr1 | 109064373 | ||||||
chr1:109064434 | T | C | 1 | a0001c0001t0015 | 1 | HG01516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*89A>G | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 4/4 | 89 | chr1 | 109064434 | ||||||
chr1:109075949 | C | T | 1 | a0001c0001t0013 | 1 | HG01167.hp2 | 5_prime_UTR_variant | MODIFIER | c.-2G>A | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 1/4 | 2 | chr1 | 109075949 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:109064891 | T | C | 3 | a0001c0001t0004g0009 a0001c0001t0004g0148 a0001c0001t0004g0149 |
8 | HG00642.hp1 HG01433.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.205-198A>G | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 3/3 | chr1 | 109064891 | |||||||
chr1:109065090 | T | C | 1 | a0001c0001t0014g0131 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.205-397A>G | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 3/3 | chr1 | 109065090 | |||||||
chr1:109065201 | C | T | 1 | a0001c0001t0001g0048 | 2 | HG02015.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.205-508G>A | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 3/3 | chr1 | 109065201 | |||||||
chr1:109065203 | G | C | 1 | a0001c0001t0004g0063 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.205-510C>G | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 3/3 | chr1 | 109065203 | |||||||
chr1:109065251 | A | G | 1 | a0001c0001t0001g0191 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.205-558T>C | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 3/3 | chr1 | 109065251 | |||||||
chr1:109065252 | G | A | 1 | a0001c0001t0001g0191 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.205-559C>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 3/3 | chr1 | 109065252 | |||||||
chr1:109065259 | G | C | 1 | a0001c0001t0001g0077 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.205-566C>G | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 3/3 | chr1 | 109065259 | |||||||
chr1:109065268 | T | C | 1 | a0001c0001t0002g0113 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.205-575A>G | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 3/3 | chr1 | 109065268 | |||||||
chr1:109065326 | A | G | 3 | a0001c0001t0002g0059 a0001c0001t0003g0011 a0001c0001t0006g0030 |
7 | HG02258.hp1 HG02615.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.205-633T>C | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 3/3 | chr1 | 109065326 | |||||||
chr1:109065366 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.205-673C>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 3/3 | chr1 | 109065366 | |||||||
chr1:109065414 | G | A | 49 | a0001c0001t0001g0112 a0001c0001t0001g0133 a0001c0001t0002g0002 others(46): Show |
96 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.204+721C>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 3/3 | chr1 | 109065414 | |||||||
chr1:109065415 | G | A | 1 | a0001c0001t0001g0191 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.204+720C>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 3/3 | chr1 | 109065415 | |||||||
chr1:109065508 | C | A | 16 | a0001c0001t0001g0122 a0001c0001t0002g0036 a0001c0001t0002g0085 others(13): Show |
19 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.204+627G>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 3/3 | chr1 | 109065508 | |||||||
chr1:109065510 | A | C | 6 | a0001c0001t0008g0023 a0001c0001t0008g0024 a0001c0001t0008g0139 others(3): Show |
10 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.204+625T>G | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 3/3 | chr1 | 109065510 | |||||||
chr1:109065519 | G | A | 3 | a0001c0001t0002g0059 a0001c0001t0003g0011 a0001c0001t0006g0030 |
7 | HG02258.hp1 HG02615.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.204+616C>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 3/3 | chr1 | 109065519 | |||||||
chr1:109065519 | G | GT | 8 | a0001c0001t0001g0027 a0001c0001t0001g0048 a0001c0001t0001g0057 others(5): Show |
13 | HG00609.hp2 HG02015.hp1 NA18939.hp2 others(10): Show |
intron_variant | MODIFIER | c.204+615dupA | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 3/3 | chr1 | 109065519 | |||||||
chr1:109065523 | C | A | 1 | a0001c0001t0005g0150 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.204+612G>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 3/3 | chr1 | 109065523 | |||||||
chr1:109065546 | GA | G | 35 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0032 others(32): Show |
57 | HG00280.hp1 HG00544.hp1 HG01070.hp2 others(54): Show |
intron_variant | MODIFIER | c.204+588delT | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 3/3 | chr1 | 109065546 | |||||||
chr1:109065643 | C | T | 1 | a0001c0001t0002g0013 | 4 | NA18959.hp2 NA18974.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.204+492G>A | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 3/3 | chr1 | 109065643 | |||||||
chr1:109065651 | G | A | 4 | a0001c0001t0002g0059 a0001c0001t0003g0011 a0001c0001t0005g0150 others(1): Show |
8 | HG02258.hp1 HG02615.hp2 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.204+484C>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 3/3 | chr1 | 109065651 | |||||||
chr1:109065661 | G | A | 64 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(61): Show |
186 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.204+474C>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 3/3 | chr1 | 109065661 | |||||||
chr1:109065768 | C | T | 1 | a0001c0001t0002g0064 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.204+367G>A | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 3/3 | chr1 | 109065768 | |||||||
chr1:109065852 | C | T | 3 | a0001c0001t0004g0088 a0001c0001t0004g0128 a0001c0001t0013g0058 |
3 | HG01167.hp2 HG03516.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.204+283G>A | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 3/3 | chr1 | 109065852 | |||||||
chr1:109065921 | C | CA | 16 | a0001c0001t0001g0014 a0001c0001t0001g0043 a0001c0001t0001g0166 others(13): Show |
27 | HG00639.hp2 HG00642.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.204+213dupT | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 3/3 | chr1 | 109065921 | |||||||
chr1:109065921 | CA | C | 27 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0032 others(24): Show |
46 | HG00280.hp1 HG00544.hp1 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.204+213delT | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 3/3 | chr1 | 109065921 | |||||||
chr1:109066007 | C | T | 1 | a0001c0001t0006g0170 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.204+128G>A | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 3/3 | chr1 | 109066007 | |||||||
chr1:109066248 | CACTT | C | 26 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0032 others(23): Show |
45 | HG00280.hp1 HG00544.hp1 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.107-20_107-17delAA others(2): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109066248 | |||||||
chr1:109066356 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.107-124C>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109066356 | |||||||
chr1:109066445 | T | C | 1 | a0001c0001t0001g0172 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.107-213A>G | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109066445 | |||||||
chr1:109066445 | TCTTC | T | 3 | a0001c0001t0002g0059 a0001c0001t0003g0011 a0001c0001t0006g0030 |
7 | HG02258.hp1 HG02615.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.107-217_107-214del others(4): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109066445 | |||||||
chr1:109066446 | C | T | 2 | a0001c0001t0004g0093 a0001c0001t0007g0018 |
4 | HG02647.hp2 HG02809.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.107-214G>A | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109066446 | |||||||
chr1:109066547 | G | T | 1 | a0001c0001t0005g0150 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.107-315C>A | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109066547 | |||||||
chr1:109066619 | T | C | 26 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0032 others(23): Show |
45 | HG00280.hp1 HG00544.hp1 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.107-387A>G | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109066619 | |||||||
chr1:109066706 | T | G | 1 | a0001c0001t0003g0099 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.107-474A>C | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109066706 | |||||||
chr1:109066755 | C | T | 2 | a0001c0001t0003g0107 a0001c0001t0015g0108 |
2 | HG01516.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.107-523G>A | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109066755 | |||||||
chr1:109066790 | C | T | 2 | a0001c0001t0004g0093 a0001c0001t0007g0018 |
4 | HG02647.hp2 HG02809.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.107-558G>A | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109066790 | |||||||
chr1:109066844 | C | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0065 |
5 | HG01099.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.107-612G>A | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109066844 | |||||||
chr1:109066853 | G | A | 2 | a0001c0001t0006g0037 a0001c0001t0006g0120 |
3 | HG03490.hp2 HG03492.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.107-621C>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109066853 | |||||||
chr1:109067010 | C | T | 7 | a0001c0001t0002g0036 a0001c0001t0002g0085 a0001c0001t0002g0089 others(4): Show |
8 | HG01891.hp1 HG02257.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.107-778G>A | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109067010 | |||||||
chr1:109067133 | G | C | 2 | a0001c0001t0001g0051 a0001c0001t0002g0173 |
3 | HG03688.hp2 HG03942.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.107-901C>G | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109067133 | |||||||
chr1:109067278 | C | A | 1 | a0001c0001t0002g0135 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.107-1046G>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109067278 | |||||||
chr1:109067278 | C | G | 1 | a0001c0001t0002g0038 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.107-1046G>C | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109067278 | |||||||
chr1:109067278 | C | T | 3 | a0001c0001t0002g0059 a0001c0001t0003g0011 a0001c0001t0006g0030 |
7 | HG02258.hp1 HG02615.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.107-1046G>A | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109067278 | |||||||
chr1:109067279 | G | A | 1 | a0001c0001t0004g0063 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.107-1047C>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109067279 | |||||||
chr1:109067363 | G | A | 20 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0032 others(17): Show |
35 | HG00280.hp1 HG00544.hp1 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.107-1131C>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109067363 | |||||||
chr1:109067436 | T | TA | 28 | a0001c0001t0001g0015 a0001c0001t0001g0043 a0001c0001t0001g0174 others(25): Show |
45 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.107-1205dupT | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109067436 | |||||||
chr1:109067436 | TA | T | 20 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0032 others(17): Show |
35 | HG00280.hp1 HG00544.hp1 HG01361.hp2 others(32): Show |
intron_variant | MODIFIER | c.107-1205delT | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109067436 | |||||||
chr1:109067448 | A | C | 6 | a0001c0001t0008g0023 a0001c0001t0008g0024 a0001c0001t0008g0139 others(3): Show |
10 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.107-1216T>G | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109067448 | |||||||
chr1:109067559 | G | C | 1 | a0001c0001t0003g0103 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.107-1327C>G | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109067559 | |||||||
chr1:109067646 | A | G | 2 | a0001c0001t0004g0093 a0001c0001t0007g0018 |
4 | HG02647.hp2 HG02809.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.107-1414T>C | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109067646 | |||||||
chr1:109067800 | T | A | 2 | a0001c0001t0001g0055 a0001c0001t0002g0185 |
3 | HG00639.hp1 HG02300.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.107-1568A>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109067800 | |||||||
chr1:109067915 | C | T | 73 | a0001c0001t0001g0012 a0001c0001t0001g0022 a0001c0001t0001g0065 others(70): Show |
129 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.107-1683G>A | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109067915 | |||||||
chr1:109068076 | A | G | 2 | a0001c0001t0001g0168 a0001c0001t0002g0169 |
2 | HG02280.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.107-1844T>C | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109068076 | |||||||
chr1:109068123 | T | G | 1 | a0001c0001t0003g0117 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.107-1891A>C | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109068123 | |||||||
chr1:109068124 | A | G | 1 | a0001c0001t0002g0074 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.107-1892T>C | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109068124 | |||||||
chr1:109068199 | G | A | 6 | a0001c0001t0008g0023 a0001c0001t0008g0024 a0001c0001t0008g0139 others(3): Show |
10 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.107-1967C>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109068199 | |||||||
chr1:109068343 | G | A | 4 | a0001c0001t0002g0121 a0001c0001t0002g0123 a0001c0001t0002g0124 others(1): Show |
4 | HG02109.hp2 HG02145.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.107-2111C>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109068343 | |||||||
chr1:109068704 | T | G | 66 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(63): Show |
188 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.107-2472A>C | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109068704 | |||||||
chr1:109068785 | T | C | 9 | a0001c0001t0001g0043 a0001c0001t0002g0059 a0001c0001t0003g0011 others(6): Show |
21 | HG00639.hp2 HG00642.hp1 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.107-2553A>G | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109068785 | |||||||
chr1:109068835 | C | T | 1 | a0001c0001t0004g0126 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.107-2603G>A | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109068835 | |||||||
chr1:109068873 | G | A | 64 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(61): Show |
186 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.107-2641C>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109068873 | |||||||
chr1:109068907 | C | T | 1 | a0001c0001t0002g0020 | 3 | HG01069.hp1 HG01071.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.107-2675G>A | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109068907 | |||||||
chr1:109068944 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.107-2712C>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109068944 | |||||||
chr1:109069202 | A | AGT | 9 | a0001c0001t0001g0012 a0001c0001t0001g0065 a0001c0001t0001g0070 others(6): Show |
16 | HG01099.hp1 HG01516.hp2 HG01517.hp2 others(13): Show |
intron_variant | MODIFIER | c.107-2972_107-2971d others(4): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109069202 | |||||||
chr1:109069202 | A | AGTGT | 1 | a0001c0001t0001g0022 | 3 | HG01884.hp2 HG02976.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.107-2974_107-2971d others(6): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109069202 | |||||||
chr1:109069202 | AGTGTGT | A | 4 | a0001c0001t0009g0031 a0001c0001t0009g0061 a0001c0001t0009g0062 others(1): Show |
5 | HG01099.hp2 HG03209.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.107-2976_107-2971d others(8): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109069202 | |||||||
chr1:109069202 | AGTGTGTG others(5): Show |
A | 66 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(63): Show |
188 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.107-2982_107-2971d others(14): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109069202 | |||||||
chr1:109069220 | T | TGC | 6 | a0001c0001t0008g0023 a0001c0001t0008g0024 a0001c0001t0008g0139 others(3): Show |
10 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.107-2990_107-2989d others(4): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109069220 | |||||||
chr1:109069236 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.107-3004C>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109069236 | |||||||
chr1:109069280 | T | C | 1 | a0001c0001t0001g0155 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.107-3048A>G | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109069280 | |||||||
chr1:109069322 | T | C | 1 | a0001c0001t0004g0126 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.107-3090A>G | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109069322 | |||||||
chr1:109069452 | T | C | 1 | a0001c0001t0007g0132 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.107-3220A>G | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109069452 | |||||||
chr1:109069527 | T | C | 1 | a0001c0001t0001g0189 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.107-3295A>G | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109069527 | |||||||
chr1:109069542 | C | G | 2 | a0001c0001t0004g0088 a0001c0001t0004g0128 |
2 | HG03516.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.107-3310G>C | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109069542 | |||||||
chr1:109069643 | T | A | 1 | a0001c0001t0004g0063 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.107-3411A>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109069643 | |||||||
chr1:109069644 | A | T | 1 | a0001c0001t0013g0058 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.107-3412T>A | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109069644 | |||||||
chr1:109069769 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.107-3537T>C | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109069769 | |||||||
chr1:109069862 | C | A | 20 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0032 others(17): Show |
35 | HG00280.hp1 HG00544.hp1 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.107-3630G>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109069862 | |||||||
chr1:109069925 | TA | T | 4 | a0001c0001t0001g0070 a0001c0001t0001g0155 a0001c0001t0002g0095 others(1): Show |
4 | NA18953.hp1 NA18977.hp1 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.107-3694delT | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109069925 | |||||||
chr1:109070099 | T | G | 1 | a0001c0001t0002g0186 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.107-3867A>C | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109070099 | |||||||
chr1:109070184 | T | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(178): Show |
389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.107-3952A>G | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109070184 | |||||||
chr1:109070214 | T | C | 2 | a0001c0001t0004g0093 a0001c0001t0007g0018 |
4 | HG02647.hp2 HG02809.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.107-3982A>G | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109070214 | |||||||
chr1:109070217 | CTTTTT | C | 20 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0032 others(17): Show |
35 | HG00280.hp1 HG00544.hp1 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.107-3990_107-3986d others(7): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109070217 | |||||||
chr1:109070287 | C | A | 64 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(61): Show |
186 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.107-4055G>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109070287 | |||||||
chr1:109070359 | C | T | 1 | a0001c0001t0004g0126 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.107-4127G>A | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109070359 | |||||||
chr1:109070391 | C | G | 26 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0032 others(23): Show |
45 | HG00280.hp1 HG00544.hp1 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.107-4159G>C | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109070391 | |||||||
chr1:109070541 | G | C | 2 | a0001c0001t0001g0060 a0001c0001t0001g0177 |
2 | HG00280.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.107-4309C>G | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109070541 | |||||||
chr1:109070554 | G | A | 2 | a0001c0001t0008g0023 a0001c0001t0012g0147 |
4 | HG02717.hp2 HG02922.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.107-4322C>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109070554 | |||||||
chr1:109070590 | C | T | 4 | a0001c0001t0008g0023 a0001c0001t0008g0139 a0001c0001t0012g0140 others(1): Show |
6 | HG02257.hp2 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.107-4358G>A | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109070590 | |||||||
chr1:109070702 | AT | A | 10 | a0001c0001t0002g0013 a0001c0001t0002g0029 a0001c0001t0002g0119 others(7): Show |
19 | HG00140.hp2 HG01109.hp1 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.106+4284delA | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109070702 | |||||||
chr1:109070844 | C | A | 58 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0014 others(55): Show |
168 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.106+4143G>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109070844 | |||||||
chr1:109071065 | G | C | 1 | a0001c0001t0006g0098 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.106+3922C>G | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071065 | |||||||
chr1:109071097 | G | A | 1 | a0001c0001t0004g0126 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.106+3890C>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071097 | |||||||
chr1:109071099 | C | T | 2 | a0001c0001t0002g0105 a0001c0001t0003g0094 |
2 | NA19062.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.106+3888G>A | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071099 | |||||||
chr1:109071157 | G | T | 1 | a0001c0001t0002g0104 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.106+3830C>A | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071157 | |||||||
chr1:109071180 | C | A | 3 | a0001c0001t0001g0053 a0001c0001t0001g0160 a0001c0001t0002g0178 |
4 | HG01257.hp1 HG01496.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.106+3807G>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071180 | |||||||
chr1:109071251 | G | C | 5 | a0001c0001t0001g0043 a0001c0001t0004g0009 a0001c0001t0004g0025 others(2): Show |
13 | HG00639.hp2 HG00642.hp1 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.106+3736C>G | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071251 | |||||||
chr1:109071298 | G | A | 3 | a0001c0001t0009g0031 a0001c0001t0009g0061 a0001c0001t0009g0062 |
4 | HG01099.hp2 HG03710.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.106+3689C>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071298 | |||||||
chr1:109071305 | G | C | 1 | a0001c0001t0003g0118 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.106+3682C>G | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071305 | |||||||
chr1:109071443 | G | GA | 15 | a0001c0001t0001g0032 a0001c0001t0001g0069 a0001c0001t0001g0073 others(12): Show |
17 | HG00642.hp1 HG00741.hp1 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.106+3543dupT | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071443 | |||||||
chr1:109071443 | GA | G | 11 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0002g0036 others(8): Show |
12 | HG01891.hp1 HG02257.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.106+3543delT | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071443 | |||||||
chr1:109071464 | G | T | 4 | a0001c0001t0009g0031 a0001c0001t0009g0061 a0001c0001t0009g0062 others(1): Show |
5 | HG01099.hp2 HG03209.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.106+3523C>A | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071464 | |||||||
chr1:109071475 | T | C | 20 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0032 others(17): Show |
35 | HG00280.hp1 HG00544.hp1 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.106+3512A>G | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071475 | |||||||
chr1:109071486 | T | A | 1 | a0001c0001t0001g0180 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.106+3501A>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071486 | |||||||
chr1:109071489 | A | G | 1 | a0001c0001t0002g0102 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.106+3498T>C | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071489 | |||||||
chr1:109071553 | T | A | 1 | a0001c0001t0001g0073 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.106+3434A>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071553 | |||||||
chr1:109071729 | G | A | 7 | a0001c0001t0001g0122 a0001c0001t0002g0121 a0001c0001t0002g0123 others(4): Show |
9 | HG02109.hp2 HG02145.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.106+3258C>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071729 | |||||||
chr1:109071754 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.106+3233G>A | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071754 | |||||||
chr1:109071801 | A | C | 1 | a0001c0001t0002g0101 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.106+3186T>G | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071801 | |||||||
chr1:109071841 | A | C | 3 | a0001c0001t0002g0019 a0001c0001t0006g0037 a0001c0001t0006g0120 |
6 | HG03490.hp2 HG03491.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.106+3146T>G | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071841 | |||||||
chr1:109071860 | G | C | 10 | a0001c0001t0002g0036 a0001c0001t0002g0064 a0001c0001t0002g0085 others(7): Show |
11 | HG01891.hp1 HG02257.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.106+3127C>G | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071860 | |||||||
chr1:109071862 | G | A | 78 | a0001c0001t0001g0012 a0001c0001t0001g0022 a0001c0001t0001g0043 others(75): Show |
142 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.106+3125C>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071862 | |||||||
chr1:109071875 | C | T | 1 | a0001c0001t0004g0063 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.106+3112G>A | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071875 | |||||||
chr1:109071896 | G | A | 2 | a0001c0001t0005g0091 a0001c0001t0007g0100 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.106+3091C>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071896 | |||||||
chr1:109071916 | C | T | 1 | a0001c0001t0002g0127 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.106+3071G>A | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071916 | |||||||
chr1:109071942 | C | T | 20 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0032 others(17): Show |
35 | HG00280.hp1 HG00544.hp1 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.106+3045G>A | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071942 | |||||||
chr1:109071956 | AAATATAT others(122): Show |
A | 1 | a0001c0001t0001g0065 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.106+2902_106+3030d others(2): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071956 | |||||||
chr1:109071956 | AAATATAT others(124): Show |
A | 1 | a0001c0001t0006g0120 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.106+2900_106+3030d others(2): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071956 | |||||||
chr1:109071957 | A | AATATATA others(3): Show |
2 | a0001c0001t0009g0031 a0001c0001t0009g0062 |
2 | HG03710.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.106+3020_106+3029d others(12): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071957 | |||||||
chr1:109071957 | AATATATA others(107): Show |
A | 2 | a0001c0001t0001g0007 a0001c0001t0002g0068 |
2 | HG01361.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.106+2916_106+3029d others(2): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071957 | |||||||
chr1:109071957 | AATATATA others(109): Show |
A | 1 | a0001c0001t0001g0007 | 3 | HG01934.hp2 HG02698.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.106+2914_106+3029d others(2): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071957 | |||||||
chr1:109071957 | AATATATA others(111): Show |
A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0078 |
2 | HG02602.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.106+2912_106+3029d others(2): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071957 | |||||||
chr1:109071957 | AATATATA others(117): Show |
A | 3 | a0001c0001t0001g0122 a0001c0001t0002g0121 a0001c0001t0002g0123 |
3 | HG02615.hp1 HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.106+2906_106+3029d others(2): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071957 | |||||||
chr1:109071957 | AATATATA others(119): Show |
A | 6 | a0001c0001t0002g0002 a0001c0001t0002g0101 a0001c0001t0002g0127 others(3): Show |
6 | HG01516.hp1 HG02155.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.106+2904_106+3029d others(2): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071957 | |||||||
chr1:109071957 | AATATATA others(121): Show |
A | 12 | a0001c0001t0001g0022 a0001c0001t0001g0109 a0001c0001t0002g0002 others(9): Show |
15 | HG00423.hp1 HG00673.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.106+2902_106+3029d others(2): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071957 | |||||||
chr1:109071957 | AATATATA others(123): Show |
A | 13 | a0001c0001t0001g0022 a0001c0001t0002g0002 a0001c0001t0002g0034 others(10): Show |
14 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.106+2900_106+3029d others(2): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071957 | |||||||
chr1:109071957 | AATATATA others(125): Show |
A | 6 | a0001c0001t0002g0002 a0001c0001t0002g0059 a0001c0001t0003g0006 others(3): Show |
8 | HG00621.hp1 HG03225.hp1 NA18522.hp2 others(5): Show |
intron_variant | MODIFIER | c.106+2898_106+3029d others(2): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071957 | |||||||
chr1:109071957 | AATATATA others(127): Show |
A | 16 | a0001c0001t0001g0133 a0001c0001t0002g0002 a0001c0001t0002g0038 others(13): Show |
22 | HG01070.hp2 HG01071.hp1 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.106+2896_106+3029d others(2): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071957 | |||||||
chr1:109071957 | AATATATA others(153): Show |
A | 46 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(43): Show |
141 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.106+2870_106+3029d others(2): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071957 | |||||||
chr1:109071957 | AATATATA others(155): Show |
A | 2 | a0001c0001t0001g0054 a0001c0001t0002g0181 |
2 | HG02080.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.106+2868_106+3029d others(2): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071957 | |||||||
chr1:109071957 | AATATATA others(157): Show |
A | 2 | a0001c0001t0002g0137 a0001c0001t0003g0138 |
2 | NA18964.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.106+2866_106+3029d others(2): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071957 | |||||||
chr1:109071957 | AATATATA others(159): Show |
A | 1 | a0001c0001t0001g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.106+2864_106+3029d others(2): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071957 | |||||||
chr1:109071958 | ATATATAT others(84): Show |
A | 1 | a0001c0001t0001g0007 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.106+2938_106+3028d others(93): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071958 | |||||||
chr1:109071958 | ATATATAT others(110): Show |
A | 1 | a0001c0001t0002g0076 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.106+2912_106+3028d others(2): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071958 | |||||||
chr1:109071958 | ATATATAT others(112): Show |
A | 2 | a0001c0001t0001g0069 a0001c0001t0001g0077 |
2 | HG01243.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.106+2910_106+3028d others(2): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071958 | |||||||
chr1:109071958 | ATATATAT others(114): Show |
A | 1 | a0001c0001t0001g0033 | 2 | HG02074.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.106+2908_106+3028d others(2): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071958 | |||||||
chr1:109071959 | T | A | 14 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0032 others(11): Show |
22 | HG00280.hp1 HG00544.hp1 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.106+3028A>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071959 | |||||||
chr1:109071959 | T | C | 25 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(22): Show |
47 | HG00597.hp1 HG00639.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.106+3028A>G | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071959 | |||||||
chr1:109071959 | TATATATA others(117): Show |
T | 4 | a0001c0001t0002g0002 a0001c0001t0002g0013 a0001c0001t0002g0042 others(1): Show |
4 | HG01952.hp1 NA18988.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.106+2904_106+3027d others(2): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071959 | |||||||
chr1:109071959 | TATATATA others(155): Show |
T | 1 | a0001c0001t0002g0002 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.106+2866_106+3027d others(2): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071959 | |||||||
chr1:109071961 | T | A | 12 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0032 others(9): Show |
20 | HG00544.hp1 HG02559.hp2 HG02818.hp1 others(17): Show |
intron_variant | MODIFIER | c.106+3026A>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071961 | |||||||
chr1:109071961 | TATATATA others(115): Show |
T | 1 | a0001c0001t0002g0002 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.106+2904_106+3025d others(2): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071961 | |||||||
chr1:109071961 | TATATATA others(153): Show |
T | 1 | a0001c0001t0008g0024 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.106+2866_106+3025d others(2): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071961 | |||||||
chr1:109071963 | T | A | 12 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0032 others(9): Show |
20 | HG00544.hp1 HG02559.hp2 HG02818.hp1 others(17): Show |
intron_variant | MODIFIER | c.106+3024A>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071963 | |||||||
chr1:109071963 | T | TATATATA others(117): Show |
1 | a0001c0001t0009g0061 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.106+3023_106+3024i others(126): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071963 | |||||||
chr1:109071963 | T | TATATATA others(73): Show |
1 | a0001c0001t0009g0090 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.106+3023_106+3024i others(82): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071963 | |||||||
chr1:109071963 | TATATATA others(113): Show |
T | 1 | a0001c0001t0002g0013 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.106+2904_106+3023d others(2): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071963 | |||||||
chr1:109071963 | TATATATA others(151): Show |
T | 21 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(18): Show |
30 | HG00597.hp1 HG00639.hp1 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.106+2866_106+3023d others(2): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071963 | |||||||
chr1:109071965 | T | A | 11 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0032 others(8): Show |
19 | HG00544.hp1 HG02559.hp2 HG04115.hp2 others(16): Show |
intron_variant | MODIFIER | c.106+3022A>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071965 | |||||||
chr1:109071965 | T | TATATATA others(205): Show |
1 | a0001c0001t0009g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.106+3021_106+3022i others(214): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071965 | |||||||
chr1:109071965 | TATATATA others(111): Show |
T | 1 | a0001c0001t0002g0013 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.106+2904_106+3021d others(2): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071965 | |||||||
chr1:109071965 | TATATATA others(149): Show |
T | 16 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0043 others(13): Show |
27 | HG00639.hp2 HG00741.hp1 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.106+2866_106+3021d others(2): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071965 | |||||||
chr1:109071967 | T | A | 10 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0032 others(7): Show |
14 | HG00544.hp1 HG04115.hp2 NA18942.hp2 others(11): Show |
intron_variant | MODIFIER | c.106+3020A>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071967 | |||||||
chr1:109071967 | TATATATA others(147): Show |
T | 10 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0046 others(7): Show |
11 | HG00642.hp1 HG01169.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.106+2866_106+3019d others(2): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071967 | |||||||
chr1:109071969 | T | A | 7 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0067 others(4): Show |
11 | HG00544.hp1 HG04115.hp2 NA18944.hp2 others(8): Show |
intron_variant | MODIFIER | c.106+3018A>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071969 | |||||||
chr1:109071969 | TATATATA others(107): Show |
T | 1 | a0001c0001t0002g0074 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.106+2904_106+3017d others(2): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071969 | |||||||
chr1:109071969 | TATATATA others(145): Show |
T | 3 | a0001c0001t0003g0117 a0001c0001t0007g0132 a0001c0001t0011g0017 |
3 | HG01928.hp2 HG03017.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.106+2866_106+3017d others(2): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071969 | |||||||
chr1:109071971 | T | A | 2 | a0001c0001t0001g0032 a0001c0001t0003g0016 |
2 | HG00544.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.106+3016A>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071971 | |||||||
chr1:109071971 | TATATACA others(105): Show |
T | 1 | a0001c0001t0001g0007 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.106+2904_106+3015d others(2): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071971 | |||||||
chr1:109071971 | TATATACA others(143): Show |
T | 9 | a0001c0001t0002g0104 a0001c0001t0003g0006 a0001c0001t0003g0115 others(6): Show |
10 | HG00741.hp2 HG01167.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.106+2866_106+3015d others(2): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071971 | |||||||
chr1:109071973 | TATACACA others(103): Show |
T | 2 | a0001c0001t0005g0091 a0001c0001t0007g0100 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.106+2904_106+3013d others(2): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071973 | |||||||
chr1:109071973 | TATACACA others(141): Show |
T | 5 | a0001c0001t0002g0036 a0001c0001t0002g0085 a0001c0001t0002g0135 others(2): Show |
6 | HG00099.hp1 HG02257.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.106+2866_106+3013d others(2): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071973 | |||||||
chr1:109071975 | TAC | T | 5 | a0001c0001t0001g0032 a0001c0001t0001g0070 a0001c0001t0001g0073 others(2): Show |
6 | NA18947.hp1 NA18974.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.106+3010_106+3011d others(4): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071975 | |||||||
chr1:109071975 | TACACACA others(33): Show |
T | 1 | a0001c0001t0005g0005 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.106+2972_106+3011d others(42): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071975 | |||||||
chr1:109071975 | TACACACA others(135): Show |
T | 17 | a0001c0001t0001g0012 a0001c0001t0001g0112 a0001c0001t0002g0002 others(14): Show |
23 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.106+2870_106+3011d others(2): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071975 | |||||||
chr1:109071975 | TACACACA others(137): Show |
T | 9 | a0001c0001t0002g0002 a0001c0001t0002g0019 a0001c0001t0002g0020 others(6): Show |
12 | HG01358.hp2 HG01981.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.106+2868_106+3011d others(2): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071975 | |||||||
chr1:109071975 | TACACACA others(139): Show |
T | 7 | a0001c0001t0001g0012 a0001c0001t0002g0035 a0001c0001t0002g0114 others(4): Show |
9 | HG00733.hp1 HG01099.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.106+2866_106+3011d others(2): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071975 | |||||||
chr1:109071977 | C | T | 5 | a0001c0001t0001g0008 a0001c0001t0001g0067 a0001c0001t0003g0016 others(2): Show |
10 | HG00280.hp1 HG01099.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.106+3010G>A | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071977 | |||||||
chr1:109071977 | CACACATA others(29): Show |
C | 1 | a0001c0001t0005g0005 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.106+2974_106+3009d others(38): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071977 | |||||||
chr1:109071979 | C | T | 9 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0067 others(6): Show |
15 | HG00280.hp1 HG02559.hp2 HG04115.hp2 others(12): Show |
intron_variant | MODIFIER | c.106+3008G>A | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071979 | |||||||
chr1:109071981 | C | T | 11 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0067 others(8): Show |
17 | HG00280.hp1 HG02559.hp2 HG02738.hp1 others(14): Show |
intron_variant | MODIFIER | c.106+3006G>A | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071981 | |||||||
chr1:109071983 | TATATATA others(31): Show |
T | 1 | a0001c0001t0005g0005 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.106+2966_106+3003d others(40): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071983 | |||||||
chr1:109071985 | TATATATA others(29): Show |
T | 3 | a0001c0001t0005g0005 a0001c0001t0005g0151 a0001c0001t0007g0044 |
5 | HG01891.hp2 HG02451.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.106+2966_106+3001d others(38): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071985 | |||||||
chr1:109071987 | T | C | 1 | a0001c0001t0005g0005 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.106+3000A>G | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071987 | |||||||
chr1:109071993 | T | C | 1 | a0001c0001t0009g0061 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.106+2994A>G | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071993 | |||||||
chr1:109071995 | T | C | 2 | a0001c0001t0009g0031 a0001c0001t0009g0090 |
2 | HG01099.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.106+2992A>G | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071995 | |||||||
chr1:109071997 | T | C | 4 | a0001c0001t0009g0031 a0001c0001t0009g0061 a0001c0001t0009g0062 others(1): Show |
5 | HG01099.hp2 HG03209.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.106+2990A>G | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071997 | |||||||
chr1:109071999 | T | C | 2 | a0001c0001t0009g0031 a0001c0001t0009g0061 |
2 | HG01099.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.106+2988A>G | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109071999 | |||||||
chr1:109072001 | TATATATA others(120): Show |
T | 1 | a0001c0001t0002g0082 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.106+2859_106+2985d others(2): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072001 | |||||||
chr1:109072007 | TATATATA others(31): Show |
T | 1 | a0001c0001t0007g0152 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.106+2942_106+2979d others(40): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072007 | |||||||
chr1:109072015 | C | T | 3 | a0001c0001t0001g0008 a0001c0001t0001g0067 a0001c0001t0009g0031 |
4 | HG01099.hp2 HG02559.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.106+2972G>A | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072015 | |||||||
chr1:109072017 | CACACATA others(121): Show |
C | 10 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0070 others(7): Show |
16 | HG00280.hp1 HG00544.hp1 HG02738.hp1 others(13): Show |
intron_variant | MODIFIER | c.106+2842_106+2969d others(2): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072017 | |||||||
chr1:109072019 | CACATATA others(119): Show |
C | 2 | a0001c0001t0001g0008 a0001c0001t0001g0067 |
3 | HG02559.hp2 HG04115.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.106+2842_106+2967d others(2): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072019 | |||||||
chr1:109072021 | C | T | 3 | a0001c0001t0005g0005 a0001c0001t0009g0061 a0001c0001t0009g0090 |
3 | HG03209.hp1 HG03209.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.106+2966G>A | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072021 | |||||||
chr1:109072031 | T | TATATACA others(103): Show |
1 | a0001c0001t0009g0062 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.106+2955_106+2956i others(112): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072031 | |||||||
chr1:109072031 | T | TATATACA others(109): Show |
1 | a0001c0001t0009g0031 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.106+2955_106+2956i others(118): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072031 | |||||||
chr1:109072049 | C | T | 1 | a0001c0001t0009g0090 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.106+2938G>A | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072049 | |||||||
chr1:109072051 | C | A | 1 | a0001c0001t0001g0007 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.106+2936G>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072051 | |||||||
chr1:109072051 | C | T | 2 | a0001c0001t0009g0031 a0001c0001t0009g0090 |
2 | HG01099.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.106+2936G>A | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072051 | |||||||
chr1:109072051 | CATATATA others(27): Show |
C | 1 | a0001c0001t0005g0005 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.106+2902_106+2935d others(36): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072051 | |||||||
chr1:109072053 | T | A | 1 | a0001c0001t0001g0007 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.106+2934A>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072053 | |||||||
chr1:109072053 | T | C | 1 | a0001c0001t0007g0152 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.106+2934A>G | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072053 | |||||||
chr1:109072055 | T | A | 1 | a0001c0001t0001g0007 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.106+2932A>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072055 | |||||||
chr1:109072057 | T | A | 1 | a0001c0001t0001g0007 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.106+2930A>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072057 | |||||||
chr1:109072059 | T | A | 1 | a0001c0001t0001g0007 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.106+2928A>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072059 | |||||||
chr1:109072059 | T | TATATACA others(25): Show |
1 | a0001c0001t0009g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.106+2927_106+2928i others(34): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072059 | |||||||
chr1:109072061 | T | A | 1 | a0001c0001t0001g0007 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.106+2926A>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072061 | |||||||
chr1:109072063 | T | TACAC | 3 | a0001c0001t0009g0031 a0001c0001t0009g0061 a0001c0001t0009g0062 |
3 | HG03710.hp2 HG03834.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.106+2923_106+2924i others(6): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072063 | |||||||
chr1:109072073 | T | A | 2 | a0001c0001t0001g0007 a0001c0001t0002g0068 |
2 | HG01361.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.106+2914A>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072073 | |||||||
chr1:109072075 | T | A | 2 | a0001c0001t0001g0007 a0001c0001t0002g0068 |
5 | HG01361.hp2 HG01934.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.106+2912A>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072075 | |||||||
chr1:109072077 | C | A | 4 | a0001c0001t0001g0007 a0001c0001t0001g0078 a0001c0001t0002g0068 others(1): Show |
8 | HG01361.hp2 HG01934.hp2 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.106+2910G>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072077 | |||||||
chr1:109072077 | C | T | 2 | a0001c0001t0009g0031 a0001c0001t0009g0090 |
2 | HG01099.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.106+2910G>A | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072077 | |||||||
chr1:109072079 | C | A | 6 | a0001c0001t0001g0007 a0001c0001t0001g0069 a0001c0001t0001g0077 others(3): Show |
10 | HG01243.hp1 HG01361.hp2 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.106+2908G>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072079 | |||||||
chr1:109072081 | C | A | 7 | a0001c0001t0001g0007 a0001c0001t0001g0033 a0001c0001t0001g0069 others(4): Show |
12 | HG01243.hp1 HG01361.hp2 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.106+2906G>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072081 | |||||||
chr1:109072082 | A | G | 1 | a0001c0001t0009g0090 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.106+2905T>C | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072082 | |||||||
chr1:109072083 | C | A | 7 | a0001c0001t0001g0007 a0001c0001t0001g0033 a0001c0001t0001g0069 others(4): Show |
12 | HG01243.hp1 HG01361.hp2 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.106+2904G>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072083 | |||||||
chr1:109072083 | C | T | 4 | a0001c0001t0009g0031 a0001c0001t0009g0061 a0001c0001t0009g0062 others(1): Show |
4 | HG03209.hp2 HG03710.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.106+2904G>A | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072083 | |||||||
chr1:109072083 | CAT | C | 2 | a0001c0001t0005g0005 a0001c0001t0007g0044 |
3 | HG01891.hp2 HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.106+2902_106+2903d others(4): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072083 | |||||||
chr1:109072085 | T | A | 6 | a0001c0001t0001g0007 a0001c0001t0001g0033 a0001c0001t0001g0069 others(3): Show |
7 | HG01243.hp1 HG01361.hp2 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.106+2902A>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072085 | |||||||
chr1:109072087 | T | A | 2 | a0001c0001t0001g0033 a0001c0001t0002g0068 |
3 | HG01361.hp2 HG02074.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.106+2900A>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072087 | |||||||
chr1:109072089 | T | A | 1 | a0001c0001t0001g0033 | 2 | HG02074.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.106+2898A>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072089 | |||||||
chr1:109072089 | T | C | 2 | a0001c0001t0002g0124 a0001c0001t0003g0125 |
2 | HG02109.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.106+2898A>G | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072089 | |||||||
chr1:109072091 | T | A | 1 | a0001c0001t0001g0033 | 2 | HG02074.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.106+2896A>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072091 | |||||||
chr1:109072097 | T | C | 1 | a0001c0001t0009g0061 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.106+2890A>G | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072097 | |||||||
chr1:109072103 | T | C | 1 | a0001c0001t0009g0090 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.106+2884A>G | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072103 | |||||||
chr1:109072105 | T | C | 1 | a0001c0001t0009g0090 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.106+2882A>G | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072105 | |||||||
chr1:109072107 | T | C | 1 | a0001c0001t0009g0090 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.106+2880A>G | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072107 | |||||||
chr1:109072111 | TATATACA others(3): Show |
T | 1 | a0001c0001t0002g0121 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.106+2866_106+2875d others(12): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072111 | |||||||
chr1:109072115 | T | C | 2 | a0001c0001t0005g0091 a0001c0001t0007g0100 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.106+2872A>G | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072115 | |||||||
chr1:109072115 | TACACAC | T | 51 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0033 others(48): Show |
86 | HG00423.hp1 HG00621.hp1 HG00673.hp2 others(83): Show |
intron_variant | MODIFIER | c.106+2866_106+2871d others(8): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072115 | |||||||
chr1:109072117 | C | T | 6 | a0001c0001t0001g0007 a0001c0001t0001g0069 a0001c0001t0001g0077 others(3): Show |
6 | HG01099.hp2 HG01243.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.106+2870G>A | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072117 | |||||||
chr1:109072119 | C | T | 22 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0069 others(19): Show |
28 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.106+2868G>A | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072119 | |||||||
chr1:109072121 | C | CATATATA others(113): Show |
1 | a0001c0001t0009g0031 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.106+2865_106+2866i others(122): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072121 | |||||||
chr1:109072121 | C | CATATATA others(117): Show |
1 | a0001c0001t0009g0061 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.106+2865_106+2866i others(126): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072121 | |||||||
chr1:109072121 | C | CATATATA others(123): Show |
1 | a0001c0001t0009g0062 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.106+2865_106+2866i others(132): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072121 | |||||||
chr1:109072121 | C | T | 75 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(72): Show |
181 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.106+2866G>A | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072121 | |||||||
chr1:109072122 | A | G | 1 | a0001c0001t0009g0090 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.106+2865T>C | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072122 | |||||||
chr1:109072123 | T | C | 4 | a0001c0001t0005g0091 a0001c0001t0005g0151 a0001c0001t0007g0100 others(1): Show |
4 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.106+2864A>G | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072123 | |||||||
chr1:109072138 | A | G | 3 | a0001c0001t0002g0059 a0001c0001t0003g0011 a0001c0001t0006g0030 |
7 | HG02258.hp1 HG02615.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.106+2849T>C | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072138 | |||||||
chr1:109072143 | T | C | 9 | a0001c0001t0001g0007 a0001c0001t0001g0033 a0001c0001t0001g0069 others(6): Show |
16 | HG01243.hp1 HG01361.hp2 HG01934.hp2 others(13): Show |
intron_variant | MODIFIER | c.106+2844A>G | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072143 | |||||||
chr1:109072145 | T | C | 9 | a0001c0001t0001g0007 a0001c0001t0001g0033 a0001c0001t0001g0069 others(6): Show |
16 | HG01243.hp1 HG01361.hp2 HG01934.hp2 others(13): Show |
intron_variant | MODIFIER | c.106+2842A>G | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072145 | |||||||
chr1:109072146 | A | G | 2 | a0001c0001t0005g0142 a0001c0001t0006g0143 |
2 | HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.106+2841T>C | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072146 | |||||||
chr1:109072317 | T | G | 2 | a0001c0001t0001g0054 a0001c0001t0002g0181 |
3 | HG02080.hp1 NA18972.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.106+2670A>C | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072317 | |||||||
chr1:109072357 | T | G | 1 | a0001c0001t0001g0022 | 3 | HG01884.hp2 HG02976.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.106+2630A>C | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072357 | |||||||
chr1:109072359 | G | A | 1 | a0001c0001t0009g0062 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.106+2628C>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072359 | |||||||
chr1:109072401 | A | G | 1 | a0001c0001t0004g0126 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.106+2586T>C | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072401 | |||||||
chr1:109072418 | T | G | 1 | a0001c0001t0005g0150 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.106+2569A>C | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072418 | |||||||
chr1:109072589 | G | A | 6 | a0001c0001t0001g0083 a0001c0001t0001g0122 a0001c0001t0002g0121 others(3): Show |
6 | HG02109.hp2 HG02145.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.106+2398C>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072589 | |||||||
chr1:109072714 | G | C | 1 | a0001c0001t0001g0182 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.106+2273C>G | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072714 | |||||||
chr1:109072743 | C | G | 1 | a0001c0001t0004g0126 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.106+2244G>C | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072743 | |||||||
chr1:109072780 | CT | C | 82 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(79): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.106+2206delA | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072780 | |||||||
chr1:109072780 | CTT | C | 67 | a0001c0001t0001g0012 a0001c0001t0001g0022 a0001c0001t0001g0055 others(64): Show |
127 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.106+2205_106+2206d others(4): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072780 | |||||||
chr1:109072780 | CTTT | C | 27 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0032 others(24): Show |
46 | HG00280.hp1 HG00544.hp1 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.106+2204_106+2206d others(5): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072780 | |||||||
chr1:109072855 | A | G | 1 | a0001c0001t0002g0089 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.106+2132T>C | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072855 | |||||||
chr1:109072859 | A | C | 26 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0032 others(23): Show |
45 | HG00280.hp1 HG00544.hp1 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.106+2128T>G | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109072859 | |||||||
chr1:109073153 | A | G | 1 | a0001c0001t0003g0157 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.106+1834T>C | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109073153 | |||||||
chr1:109073262 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.106+1725C>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109073262 | |||||||
chr1:109073410 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.106+1577G>A | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109073410 | |||||||
chr1:109073519 | G | A | 7 | a0001c0001t0004g0088 a0001c0001t0004g0128 a0001c0001t0004g0130 others(4): Show |
7 | HG00099.hp1 HG01167.hp2 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.106+1468C>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109073519 | |||||||
chr1:109073605 | G | A | 1 | a0001c0001t0001g0187 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.106+1382C>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109073605 | |||||||
chr1:109073705 | C | T | 62 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(59): Show |
184 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.106+1282G>A | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109073705 | |||||||
chr1:109073857 | C | T | 1 | a0001c0001t0001g0161 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.106+1130G>A | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109073857 | |||||||
chr1:109073885 | G | A | 2 | a0001c0001t0001g0133 a0001c0001t0002g0134 |
2 | NA18943.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.106+1102C>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109073885 | |||||||
chr1:109073911 | G | A | 3 | a0001c0001t0002g0059 a0001c0001t0003g0011 a0001c0001t0006g0030 |
7 | HG02258.hp1 HG02615.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.106+1076C>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109073911 | |||||||
chr1:109073928 | G | T | 26 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0032 others(23): Show |
45 | HG00280.hp1 HG00544.hp1 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.106+1059C>A | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109073928 | |||||||
chr1:109073942 | A | AC | 18 | a0001c0001t0001g0010 a0001c0001t0001g0067 a0001c0001t0001g0069 others(15): Show |
26 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.106+1044dupG | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109073942 | |||||||
chr1:109073946 | C | T | 1 | a0001c0001t0003g0084 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.106+1041G>A | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109073946 | |||||||
chr1:109073994 | A | G | 6 | a0001c0001t0008g0023 a0001c0001t0008g0024 a0001c0001t0008g0139 others(3): Show |
10 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.106+993T>C | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109073994 | |||||||
chr1:109073995 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.106+992T>C | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109073995 | |||||||
chr1:109074018 | C | G | 4 | a0001c0001t0008g0023 a0001c0001t0008g0139 a0001c0001t0012g0140 others(1): Show |
6 | HG02257.hp2 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.106+969G>C | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109074018 | |||||||
chr1:109074057 | G | A | 1 | a0001c0001t0002g0135 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.106+930C>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109074057 | |||||||
chr1:109074166 | T | G | 2 | a0001c0001t0003g0136 a0001c0001t0003g0146 |
2 | NA18940.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.106+821A>C | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109074166 | |||||||
chr1:109074191 | A | G | 4 | a0001c0001t0002g0034 a0001c0001t0002g0080 a0001c0001t0002g0082 others(1): Show |
5 | HG02523.hp1 NA18941.hp2 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.106+796T>C | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109074191 | |||||||
chr1:109074207 | G | C | 1 | a0001c0001t0005g0150 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.106+780C>G | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109074207 | |||||||
chr1:109074240 | C | A | 1 | a0001c0001t0002g0041 | 2 | NA18612.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.106+747G>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109074240 | |||||||
chr1:109074258 | A | C | 1 | a0001c0001t0002g0066 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.106+729T>G | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109074258 | |||||||
chr1:109074338 | G | A | 1 | a0001c0001t0012g0147 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.106+649C>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109074338 | |||||||
chr1:109074345 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.106+642C>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109074345 | |||||||
chr1:109074385 | G | C | 6 | a0001c0001t0002g0059 a0001c0001t0002g0137 a0001c0001t0003g0011 others(3): Show |
10 | HG02258.hp1 HG02615.hp2 HG03139.hp2 others(7): Show |
intron_variant | MODIFIER | c.106+602C>G | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109074385 | |||||||
chr1:109074420 | C | T | 20 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0032 others(17): Show |
35 | HG00280.hp1 HG00544.hp1 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.106+567G>A | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109074420 | |||||||
chr1:109074590 | A | T | 1 | a0001c0001t0001g0032 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.106+397T>A | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109074590 | |||||||
chr1:109074622 | C | A | 1 | a0001c0001t0013g0058 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.106+365G>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109074622 | |||||||
chr1:109074779 | C | CA | 14 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0002g0042 others(11): Show |
19 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.106+207dupT | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109074779 | |||||||
chr1:109074779 | C | CAA | 5 | a0001c0001t0001g0043 a0001c0001t0004g0009 a0001c0001t0004g0025 others(2): Show |
13 | HG00639.hp2 HG00642.hp1 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.106+206_106+207dup others(2): Show |
TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 2/3 | chr1 | 109074779 | |||||||
chr1:109075133 | A | AT | 5 | a0001c0001t0001g0012 a0001c0001t0001g0065 a0001c0001t0002g0064 others(2): Show |
8 | HG01099.hp1 HG01516.hp2 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.28-69dupA | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 1/3 | chr1 | 109075133 | |||||||
chr1:109075155 | A | G | 3 | a0001c0001t0009g0031 a0001c0001t0009g0061 a0001c0001t0009g0062 |
4 | HG01099.hp2 HG03710.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.28-90T>C | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 1/3 | chr1 | 109075155 | |||||||
chr1:109075177 | G | A | 1 | a0001c0001t0005g0150 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.28-112C>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 1/3 | chr1 | 109075177 | |||||||
chr1:109075288 | C | T | 1 | a0001c0001t0002g0156 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.28-223G>A | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 1/3 | chr1 | 109075288 | |||||||
chr1:109075300 | G | T | 1 | a0001c0001t0001g0155 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.28-235C>A | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 1/3 | chr1 | 109075300 | |||||||
chr1:109075424 | T | C | 2 | a0001c0001t0001g0056 a0001c0001t0002g0190 |
3 | HG01256.hp2 HG01258.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.28-359A>G | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 1/3 | chr1 | 109075424 | |||||||
chr1:109075462 | C | G | 1 | a0001c0001t0001g0154 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.28-397G>C | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 1/3 | chr1 | 109075462 | |||||||
chr1:109075469 | T | C | 3 | a0001c0001t0001g0057 a0001c0001t0001g0191 a0001c0001t0001g0192 |
4 | HG00609.hp2 NA18967.hp1 NA18987.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-404A>G | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 1/3 | chr1 | 109075469 | |||||||
chr1:109075635 | C | T | 187 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(184): Show |
399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.27+286G>A | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 1/3 | chr1 | 109075635 | |||||||
chr1:109075652 | T | C | 1 | a0001c0001t0002g0153 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.27+269A>G | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 1/3 | chr1 | 109075652 | |||||||
chr1:109075686 | G | A | 62 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(59): Show |
184 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.27+235C>T | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 1/3 | chr1 | 109075686 | |||||||
chr1:109075866 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.27+55T>C | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 1/3 | chr1 | 109075866 | |||||||
chr1:109075870 | A | C | 3 | a0001c0001t0002g0059 a0001c0001t0003g0011 a0001c0001t0006g0030 |
7 | HG02258.hp1 HG02615.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.27+51T>G | TAF13 | ENSG00000197780.11 | transcript | ENST00000338366.6 | protein_coding | 1/3 | chr1 | 109075870 |