Item | Value |
---|---|
geneid | 129685 |
ensemblid | ENSG00000137413.17 |
hgncid | 17300 |
symbol | TAF8 |
name | TATA-box binding protein associated factor 8 |
refseq_nuc | NM_138572.3 |
refseq_prot | NP_612639.2 |
ensembl_nuc | ENST00000372977.8 |
ensembl_prot | ENSP00000362068.3 |
mane_status | MANE Select |
chr | chr6 |
start | 42050524 |
end | 42083272 |
strand | + |
ver | v1.2 |
region | chr6:42050524-42083272 |
region5000 | chr6:42045524-42088272 |
regionname0 | TAF8_chr6_42050524_42083272 |
regionname5000 | TAF8_chr6_42045524_42088272 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 930 | 332 | 35 | 62 | 190 | 13 | 32 | TAF8_chr6_42045524_42088272 | TAF8 | ATGGC others(925): Show |
chr6 | 42045524 | 42088272 | ||
a0001c0002 | 1/1 | 930 | 119 | 59 | 18 | 23 | 5 | 12 | TAF8_chr6_42045524_42088272 | TAF8 | ATGGC others(925): Show |
chr6 | 42045524 | 42088272 | ||
a0001c0003 | 0/0 | 930 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ATGGC others(925): Show |
chr6 | 42045524 | 42088272 | ||
a0001c0004 | 0/0 | 930 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ATGGC others(925): Show |
chr6 | 42045524 | 42088272 | ||
a0001c0005 | 0/0 | 930 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ATGGC others(925): Show |
chr6 | 42045524 | 42088272 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6678 | 132 | 2 | 32 | 73 | 10 | 15 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6673): Show |
chr6 | 42045524 | 42088272 |
a0001c0001t0002 | 0/0 | 6683 | 43 | 0 | 13 | 27 | 0 | 3 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6678): Show |
chr6 | 42045524 | 42088272 |
a0001c0001t0003 | 0/0 | 6684 | 41 | 1 | 1 | 36 | 0 | 3 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6679): Show |
chr6 | 42045524 | 42088272 |
a0001c0001t0005 | 0/0 | 6683 | 23 | 4 | 1 | 18 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6678): Show |
chr6 | 42045524 | 42088272 |
a0001c0001t0006 | 0/0 | 6683 | 19 | 3 | 6 | 3 | 2 | 5 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6678): Show |
chr6 | 42045524 | 42088272 |
a0001c0001t0008 | 0/0 | 6678 | 10 | 1 | 3 | 6 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6673): Show |
chr6 | 42045524 | 42088272 |
a0001c0001t0010 | 0/0 | 6683 | 9 | 0 | 0 | 8 | 1 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6678): Show |
chr6 | 42045524 | 42088272 |
a0001c0001t0012 | 0/0 | 6682 | 7 | 6 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6677): Show |
chr6 | 42045524 | 42088272 |
a0001c0001t0013 | 0/0 | 6683 | 6 | 6 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6678): Show |
chr6 | 42045524 | 42088272 |
a0001c0001t0019 | 0/0 | 6677 | 3 | 0 | 0 | 3 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6672): Show |
chr6 | 42045524 | 42088272 |
a0001c0001t0020 | 0/0 | 6682 | 3 | 3 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6677): Show |
chr6 | 42045524 | 42088272 |
a0001c0001t0021 | 0/0 | 6684 | 3 | 3 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6679): Show |
chr6 | 42045524 | 42088272 |
a0001c0001t0022 | 0/0 | 6678 | 3 | 0 | 2 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6673): Show |
chr6 | 42045524 | 42088272 |
a0001c0001t0025 | 0/0 | 6678 | 2 | 0 | 0 | 0 | 0 | 2 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6673): Show |
chr6 | 42045524 | 42088272 |
a0001c0001t0030 | 0/0 | 6683 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6678): Show |
chr6 | 42045524 | 42088272 |
a0001c0001t0031 | 0/0 | 6684 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6679): Show |
chr6 | 42045524 | 42088272 |
a0001c0001t0032 | 0/0 | 6684 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6679): Show |
chr6 | 42045524 | 42088272 |
a0001c0001t0033 | 0/0 | 6682 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6677): Show |
chr6 | 42045524 | 42088272 |
a0001c0001t0034 | 0/0 | 6683 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6678): Show |
chr6 | 42045524 | 42088272 |
a0001c0001t0035 | 0/0 | 6684 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6679): Show |
chr6 | 42045524 | 42088272 |
a0001c0001t0041 | 0/0 | 6678 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6673): Show |
chr6 | 42045524 | 42088272 |
a0001c0001t0042 | 0/0 | 6677 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6672): Show |
chr6 | 42045524 | 42088272 |
a0001c0001t0043 | 0/0 | 6682 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6677): Show |
chr6 | 42045524 | 42088272 |
a0001c0001t0044 | 0/0 | 6682 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6677): Show |
chr6 | 42045524 | 42088272 |
a0001c0001t0045 | 0/0 | 6681 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6676): Show |
chr6 | 42045524 | 42088272 |
a0001c0001t0046 | 0/0 | 6683 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6678): Show |
chr6 | 42045524 | 42088272 |
a0001c0001t0048 | 0/0 | 6679 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6674): Show |
chr6 | 42045524 | 42088272 |
a0001c0001t0049 | 0/0 | 6682 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6677): Show |
chr6 | 42045524 | 42088272 |
a0001c0001t0050 | 0/0 | 6678 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6673): Show |
chr6 | 42045524 | 42088272 |
a0001c0001t0051 | 0/0 | 6678 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6673): Show |
chr6 | 42045524 | 42088272 |
a0001c0001t0053 | 0/0 | 6678 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6673): Show |
chr6 | 42045524 | 42088272 |
a0001c0001t0054 | 0/0 | 6680 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6675): Show |
chr6 | 42045524 | 42088272 |
a0001c0001t0055 | 0/0 | 6678 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6673): Show |
chr6 | 42045524 | 42088272 |
a0001c0001t0056 | 0/0 | 6684 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6679): Show |
chr6 | 42045524 | 42088272 |
a0001c0001t0057 | 0/0 | 6683 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6678): Show |
chr6 | 42045524 | 42088272 |
a0001c0001t0058 | 0/0 | 6726 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6721): Show |
chr6 | 42045524 | 42088272 |
a0001c0001t0059 | 0/0 | 6679 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6674): Show |
chr6 | 42045524 | 42088272 |
a0001c0001t0060 | 0/0 | 6683 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6678): Show |
chr6 | 42045524 | 42088272 |
a0001c0001t0061 | 0/0 | 6683 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6678): Show |
chr6 | 42045524 | 42088272 |
a0001c0001t0062 | 0/0 | 6679 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6674): Show |
chr6 | 42045524 | 42088272 |
a0001c0001t0063 | 0/0 | 6677 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6672): Show |
chr6 | 42045524 | 42088272 |
a0001c0001t0077 | 0/0 | 6676 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6671): Show |
chr6 | 42045524 | 42088272 |
a0001c0002t0004 | 0/0 | 6677 | 35 | 5 | 11 | 11 | 4 | 4 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6672): Show |
chr6 | 42045524 | 42088272 |
a0001c0002t0007 | 0/0 | 6678 | 13 | 13 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6673): Show |
chr6 | 42045524 | 42088272 |
a0001c0002t0009 | 0/0 | 6676 | 10 | 3 | 2 | 1 | 1 | 3 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6671): Show |
chr6 | 42045524 | 42088272 |
a0001c0002t0011 | 0/0 | 6677 | 7 | 0 | 0 | 7 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6672): Show |
chr6 | 42045524 | 42088272 |
a0001c0002t0014 | 0/0 | 6675 | 6 | 6 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6670): Show |
chr6 | 42045524 | 42088272 |
a0001c0002t0015 | 0/0 | 6676 | 6 | 6 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6671): Show |
chr6 | 42045524 | 42088272 |
a0001c0002t0016 | 0/0 | 6674 | 5 | 5 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6669): Show |
chr6 | 42045524 | 42088272 |
a0001c0002t0017 | 0/0 | 6675 | 4 | 4 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6670): Show |
chr6 | 42045524 | 42088272 |
a0001c0002t0018 | 0/0 | 6679 | 4 | 3 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6674): Show |
chr6 | 42045524 | 42088272 |
a0001c0002t0023 | 0/0 | 6674 | 2 | 2 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6669): Show |
chr6 | 42045524 | 42088272 |
a0001c0002t0024 | 0/0 | 6676 | 2 | 0 | 0 | 2 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6671): Show |
chr6 | 42045524 | 42088272 |
a0001c0002t0026 | 0/0 | 6676 | 2 | 2 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6671): Show |
chr6 | 42045524 | 42088272 |
a0001c0002t0027 | 0/0 | 6678 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6673): Show |
chr6 | 42045524 | 42088272 |
a0001c0002t0028 | 0/0 | 6673 | 2 | 0 | 1 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6668): Show |
chr6 | 42045524 | 42088272 |
a0001c0002t0029 | 0/0 | 6676 | 2 | 1 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6671): Show |
chr6 | 42045524 | 42088272 |
a0001c0002t0036 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6670): Show |
chr6 | 42045524 | 42088272 |
a0001c0002t0037 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6670): Show |
chr6 | 42045524 | 42088272 |
a0001c0002t0038 | 0/0 | 6678 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6673): Show |
chr6 | 42045524 | 42088272 |
a0001c0002t0039 | 0/0 | 6675 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6670): Show |
chr6 | 42045524 | 42088272 |
a0001c0002t0040 | 0/0 | 6677 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6672): Show |
chr6 | 42045524 | 42088272 |
a0001c0002t0064 | 0/0 | 6677 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6672): Show |
chr6 | 42045524 | 42088272 |
a0001c0002t0065 | 1/0 | 6678 | 1 | 0 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6673): Show |
chr6 | 42045524 | 42088272 |
a0001c0002t0066 | 0/0 | 6677 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6672): Show |
chr6 | 42045524 | 42088272 |
a0001c0002t0067 | 0/0 | 6678 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6673): Show |
chr6 | 42045524 | 42088272 |
a0001c0002t0068 | 0/0 | 6677 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6672): Show |
chr6 | 42045524 | 42088272 |
a0001c0002t0069 | 0/0 | 6676 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6671): Show |
chr6 | 42045524 | 42088272 |
a0001c0002t0070 | 0/0 | 6677 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6672): Show |
chr6 | 42045524 | 42088272 |
a0001c0002t0071 | 0/0 | 6678 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6673): Show |
chr6 | 42045524 | 42088272 |
a0001c0002t0072 | 0/0 | 6677 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6672): Show |
chr6 | 42045524 | 42088272 |
a0001c0002t0073 | 0/0 | 6673 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6668): Show |
chr6 | 42045524 | 42088272 |
a0001c0002t0074 | 0/0 | 6676 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6671): Show |
chr6 | 42045524 | 42088272 |
a0001c0002t0075 | 0/1 | 6680 | 1 | 0 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6675): Show |
chr6 | 42045524 | 42088272 |
a0001c0002t0076 | 0/0 | 6676 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6671): Show |
chr6 | 42045524 | 42088272 |
a0001c0003t0047 | 0/0 | 6676 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6671): Show |
chr6 | 42045524 | 42088272 |
a0001c0004t0052 | 0/0 | 6678 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6673): Show |
chr6 | 42045524 | 42088272 |
a0001c0005t0027 | 0/0 | 6678 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | ACACT others(6673): Show |
chr6 | 42045524 | 42088272 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 9 | 0 | 2 | 4 | 2 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0002 | 0/0 | 7 | 0 | 5 | 0 | 0 | 2 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0006 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0011 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0002g0003 | 0/0 | 9 | 0 | 7 | 2 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0002g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0002g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0003g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0003g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0003g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0003g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0003g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0003g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0005g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0005g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0005g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0005g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0005g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0005g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0005g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0005g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0005g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0005g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0005g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0005g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0005g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0005g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0005g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0005g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0005g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0005g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0005g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0005g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0005g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0005g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0006g0015 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0006g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0006g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0006g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0006g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0006g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0006g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0006g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0006g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0006g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0006g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0006g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0006g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0006g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0006g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0008g0001 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0008g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0008g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0008g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0008g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0008g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0008g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0010g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0010g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0010g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0010g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0010g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0010g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0010g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0010g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0012g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0012g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0012g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0012g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0012g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0013g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0013g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0013g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0013g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0013g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0013g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0019g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0019g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0019g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0020g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0020g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0020g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0021g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0021g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0021g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0022g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0022g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0022g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0025g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0030g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0031g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0032g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0033g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0034g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0035g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0041g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0042g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0043g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0044g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0045g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0046g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0048g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0049g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0050g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0051g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0053g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0054g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0055g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0056g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0057g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0058g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0059g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0060g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0061g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0062g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0063g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0001t0077g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0004g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0004g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0004g0037 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0004g0038 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0004g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0004g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0004g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0004g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0004g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0004g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0004g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0004g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0004g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0004g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0004g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0004g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0004g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0004g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0004g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0004g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0004g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0004g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0004g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0004g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0004g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0004g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0004g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0004g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0004g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0007g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0007g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0007g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0007g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0007g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0007g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0007g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0007g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0007g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0007g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0007g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0007g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0009g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0009g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0009g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0009g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0009g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0009g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0009g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0009g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0009g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0009g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0011g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0011g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0011g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0011g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0011g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0011g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0014g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0014g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0014g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0014g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0014g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0014g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0015g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0015g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0016g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0016g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0016g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0016g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0016g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0017g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0017g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0017g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0018g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0018g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0018g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0023g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0023g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0024g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0024g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0026g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0026g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0027g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0028g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0028g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0029g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0029g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0036g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0037g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0038g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0039g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0040g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0064g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0065g0342 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0066g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0067g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0068g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0069g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0070g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0071g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0072g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0073g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0074g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0075g0187 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0002t0076g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0003t0047g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0004t0052g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
a0001c0005t0027g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0004 | g0038 | EUR | GBR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | GBR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG00140 | hp1 | a0001 | c0002 | t0004 | g0102 | EUR | GBR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG00140 | hp2 | a0001 | c0002 | t0004 | g0019 | EUR | GBR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG00280 | hp1 | a0001 | c0001 | t0006 | g0246 | EUR | FIN | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG00280 | hp2 | a0001 | c0002 | t0009 | g0300 | EUR | FIN | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG00323 | hp1 | a0001 | c0001 | t0010 | g0071 | EUR | FIN | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG00323 | hp2 | a0001 | c0002 | t0004 | g0076 | EUR | FIN | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG00408 | hp2 | a0001 | c0002 | t0072 | g0285 | EAS | CHS | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | CHS | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG00423 | hp2 | a0001 | c0001 | t0005 | g0308 | EAS | CHS | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG00438 | hp1 | a0001 | c0001 | t0005 | g0321 | EAS | CHS | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG00544 | hp1 | a0001 | c0001 | t0003 | g0080 | EAS | CHS | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | CHS | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG00597 | hp1 | a0001 | c0001 | t0051 | g0296 | EAS | CHS | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0224 | EAS | CHS | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | CHS | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | CHS | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG00621 | hp1 | a0001 | c0001 | t0010 | g0203 | EAS | CHS | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG00621 | hp2 | a0001 | c0001 | t0003 | g0111 | EAS | CHS | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG00639 | hp1 | a0001 | c0002 | t0004 | g0181 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG00642 | hp1 | a0001 | c0001 | t0012 | g0031 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG00673 | hp1 | a0001 | c0001 | t0003 | g0068 | EAS | CHS | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG00673 | hp2 | a0001 | c0001 | t0003 | g0048 | EAS | CHS | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG00733 | hp1 | a0001 | c0001 | t0022 | g0001 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0099 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0238 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0347 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG00738 | hp2 | a0001 | c0001 | t0006 | g0077 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG00741 | hp1 | a0001 | c0002 | t0028 | g0183 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG00741 | hp2 | a0001 | c0002 | t0018 | g0155 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0307 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01081 | hp2 | a0001 | c0001 | t0056 | g0160 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0142 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0231 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01106 | hp2 | a0001 | c0001 | t0006 | g0074 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01167 | hp1 | a0001 | c0002 | t0004 | g0059 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01169 | hp1 | a0001 | c0002 | t0009 | g0188 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01169 | hp2 | a0001 | c0002 | t0004 | g0079 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01175 | hp1 | a0001 | c0001 | t0006 | g0196 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01175 | hp2 | a0001 | c0002 | t0074 | g0272 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01192 | hp1 | a0001 | c0002 | t0004 | g0026 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01192 | hp2 | a0001 | c0001 | t0006 | g0066 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01243 | hp1 | a0001 | c0001 | t0006 | g0271 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01243 | hp2 | a0001 | c0002 | t0070 | g0299 | AMR | PUR | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01255 | hp1 | a0001 | c0001 | t0005 | g0154 | AMR | CLM | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0302 | AMR | CLM | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01258 | hp1 | a0001 | c0001 | t0006 | g0186 | AMR | CLM | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0228 | AMR | CLM | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01361 | hp1 | a0001 | c0002 | t0004 | g0019 | AMR | CLM | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01361 | hp2 | a0001 | c0001 | t0022 | g0014 | AMR | CLM | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | CLM | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0017 | EUR | IBS | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | IBS | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0305 | EUR | IBS | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | IBS | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01884 | hp2 | a0001 | c0001 | t0021 | g0306 | AFR | ACB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01891 | hp1 | a0001 | c0002 | t0023 | g0169 | AFR | ACB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01891 | hp2 | a0001 | c0001 | t0012 | g0310 | AFR | ACB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01928 | hp1 | a0001 | c0001 | t0053 | g0006 | AMR | PEL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01934 | hp1 | a0001 | c0002 | t0004 | g0026 | AMR | PEL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01934 | hp2 | a0001 | c0002 | t0029 | g0269 | AMR | PEL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01943 | hp2 | a0001 | c0001 | t0008 | g0209 | AMR | PEL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01952 | hp2 | a0001 | c0001 | t0008 | g0018 | AMR | PEL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01975 | hp1 | a0001 | c0002 | t0004 | g0204 | AMR | PEL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01975 | hp2 | a0001 | c0002 | t0004 | g0286 | AMR | PEL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01978 | hp2 | a0001 | c0002 | t0004 | g0288 | AMR | PEL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01981 | hp1 | a0001 | c0001 | t0063 | g0184 | AMR | PEL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0206 | AMR | PEL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02015 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | KHV | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | KHV | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | KHV | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02055 | hp1 | a0001 | c0002 | t0004 | g0037 | AFR | ACB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02055 | hp2 | a0001 | c0004 | t0052 | g0195 | AFR | ACB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02056 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | KHV | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02056 | hp2 | a0001 | c0001 | t0010 | g0128 | EAS | KHV | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | KHV | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02074 | hp1 | a0001 | c0001 | t0003 | g0070 | EAS | KHV | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02080 | hp2 | a0001 | c0001 | t0010 | g0081 | EAS | KHV | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02083 | hp2 | a0001 | c0001 | t0003 | g0094 | EAS | KHV | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | KHV | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02135 | hp1 | a0001 | c0001 | t0003 | g0087 | EAS | KHV | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | KHV | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02145 | hp1 | a0001 | c0001 | t0020 | g0332 | AFR | ACB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02145 | hp2 | a0001 | c0002 | t0066 | g0200 | AFR | ACB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02148 | hp1 | a0001 | c0001 | t0003 | g0316 | AMR | PEL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02148 | hp2 | a0001 | c0001 | t0008 | g0001 | AMR | PEL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | CDX | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02155 | hp2 | a0001 | c0002 | t0004 | g0312 | EAS | CDX | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CDX | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02257 | hp1 | a0001 | c0001 | t0006 | g0025 | AFR | ACB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02257 | hp2 | a0001 | c0002 | t0038 | g0175 | AFR | ACB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02258 | hp1 | a0001 | c0002 | t0007 | g0158 | AFR | ACB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02258 | hp2 | a0001 | c0002 | t0018 | g0130 | AFR | ACB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02273 | hp2 | a0001 | c0002 | t0004 | g0278 | AMR | PEL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02280 | hp1 | a0001 | c0002 | t0007 | g0265 | AFR | ACB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02280 | hp2 | a0001 | c0001 | t0034 | g0297 | AFR | ACB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02300 | hp1 | a0001 | c0002 | t0004 | g0277 | AMR | PEL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02451 | hp1 | a0001 | c0002 | t0026 | g0137 | AFR | ACB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02451 | hp2 | a0001 | c0002 | t0076 | g0242 | AFR | ACB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | KHV | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02572 | hp1 | a0001 | c0001 | t0020 | g0331 | AFR | GWD | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02572 | hp2 | a0001 | c0001 | t0057 | g0163 | AFR | GWD | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02602 | hp1 | a0001 | c0002 | t0009 | g0194 | SAS | PJL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0314 | SAS | PJL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02615 | hp1 | a0001 | c0002 | t0004 | g0322 | AFR | GWD | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02615 | hp2 | a0001 | c0002 | t0073 | g0257 | AFR | GWD | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02622 | hp1 | a0001 | c0002 | t0039 | g0339 | AFR | GWD | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02622 | hp2 | a0001 | c0002 | t0009 | g0151 | AFR | GWD | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02630 | hp1 | a0001 | c0002 | t0067 | g0337 | AFR | GWD | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02630 | hp2 | a0001 | c0001 | t0077 | g0170 | AFR | GWD | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02647 | hp1 | a0001 | c0002 | t0014 | g0259 | AFR | GWD | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02647 | hp2 | a0001 | c0001 | t0012 | g0030 | AFR | GWD | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0292 | SAS | PJL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02717 | hp1 | a0001 | c0001 | t0013 | g0161 | AFR | GWD | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02717 | hp2 | a0001 | c0002 | t0014 | g0152 | AFR | GWD | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02723 | hp1 | a0001 | c0002 | t0029 | g0268 | AFR | GWD | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02723 | hp2 | a0001 | c0001 | t0013 | g0344 | AFR | GWD | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02735 | hp1 | a0001 | c0001 | t0003 | g0276 | SAS | PJL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02735 | hp2 | a0001 | c0001 | t0006 | g0140 | SAS | PJL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02738 | hp1 | a0001 | c0001 | t0061 | g0281 | SAS | PJL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0143 | SAS | PJL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02809 | hp1 | a0001 | c0001 | t0005 | g0178 | AFR | GWD | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02809 | hp2 | a0001 | c0002 | t0017 | g0264 | AFR | GWD | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02886 | hp1 | a0001 | c0001 | t0059 | g0201 | AFR | GWD | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02886 | hp2 | a0001 | c0001 | t0013 | g0338 | AFR | GWD | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02895 | hp1 | a0001 | c0002 | t0007 | g0171 | AFR | GWD | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02895 | hp2 | a0001 | c0002 | t0014 | g0252 | AFR | GWD | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02896 | hp1 | a0001 | c0002 | t0009 | g0153 | AFR | GWD | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02896 | hp2 | a0001 | c0002 | t0007 | g0034 | AFR | GWD | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02922 | hp1 | a0001 | c0003 | t0047 | g0273 | AFR | ESN | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02922 | hp2 | a0001 | c0001 | t0013 | g0147 | AFR | ESN | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02965 | hp1 | a0001 | c0002 | t0007 | g0343 | AFR | ESN | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02965 | hp2 | a0001 | c0002 | t0007 | g0159 | AFR | ESN | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02970 | hp1 | a0001 | c0002 | t0007 | g0086 | AFR | ESN | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02970 | hp2 | a0001 | c0001 | t0013 | g0295 | AFR | ESN | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02976 | hp1 | a0001 | c0002 | t0015 | g0010 | AFR | ESN | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02976 | hp2 | a0001 | c0002 | t0016 | g0131 | AFR | ESN | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG03017 | hp1 | a0001 | c0002 | t0004 | g0038 | SAS | PJL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0061 | SAS | PJL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG03041 | hp1 | a0001 | c0001 | t0005 | g0253 | AFR | GWD | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG03041 | hp2 | a0001 | c0002 | t0015 | g0010 | AFR | GWD | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG03098 | hp1 | a0001 | c0001 | t0003 | g0317 | AFR | MSL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG03098 | hp2 | a0001 | c0002 | t0014 | g0149 | AFR | MSL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG03130 | hp1 | a0001 | c0002 | t0026 | g0345 | AFR | ESN | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG03130 | hp2 | a0001 | c0002 | t0015 | g0010 | AFR | ESN | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG03139 | hp1 | a0001 | c0002 | t0017 | g0165 | AFR | ESN | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG03139 | hp2 | a0001 | c0002 | t0023 | g0167 | AFR | ESN | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG03195 | hp1 | a0001 | c0002 | t0004 | g0177 | AFR | ESN | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG03195 | hp2 | a0001 | c0002 | t0007 | g0034 | AFR | ESN | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG03209 | hp1 | a0001 | c0002 | t0007 | g0146 | AFR | MSL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG03209 | hp2 | a0001 | c0001 | t0062 | g0340 | AFR | MSL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG03225 | hp1 | a0001 | c0001 | t0005 | g0333 | AFR | MSL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG03225 | hp2 | a0001 | c0002 | t0016 | g0164 | AFR | MSL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG03239 | hp1 | a0001 | c0002 | t0009 | g0189 | SAS | PJL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG03239 | hp2 | a0001 | c0002 | t0068 | g0115 | SAS | PJL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG03453 | hp1 | a0001 | c0002 | t0007 | g0263 | AFR | MSL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG03453 | hp2 | a0001 | c0001 | t0013 | g0336 | AFR | MSL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG03486 | hp1 | a0001 | c0002 | t0016 | g0174 | AFR | MSL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG03486 | hp2 | a0001 | c0001 | t0006 | g0025 | AFR | MSL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG03490 | hp1 | a0001 | c0002 | t0069 | g0219 | SAS | PJL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG03490 | hp2 | a0001 | c0001 | t0025 | g0002 | SAS | PJL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG03491 | hp1 | a0001 | c0002 | t0028 | g0182 | SAS | PJL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG03491 | hp2 | a0001 | c0001 | t0006 | g0040 | SAS | PJL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG03492 | hp1 | a0001 | c0001 | t0006 | g0040 | SAS | PJL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG03492 | hp2 | a0001 | c0001 | t0025 | g0002 | SAS | PJL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG03516 | hp1 | a0001 | c0002 | t0009 | g0270 | AFR | ESN | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG03516 | hp2 | a0001 | c0001 | t0012 | g0030 | AFR | ESN | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG03540 | hp1 | a0001 | c0002 | t0016 | g0173 | AFR | GWD | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG03540 | hp2 | a0001 | c0001 | t0012 | g0267 | AFR | GWD | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG03579 | hp1 | a0001 | c0002 | t0037 | g0166 | AFR | MSL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG03579 | hp2 | a0001 | c0002 | t0016 | g0162 | AFR | MSL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG03654 | hp1 | a0001 | c0001 | t0031 | g0279 | SAS | PJL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG03669 | hp2 | a0001 | c0001 | t0006 | g0318 | SAS | PJL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | STU | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG03688 | hp2 | a0001 | c0002 | t0040 | g0256 | SAS | STU | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0287 | SAS | PJL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG03710 | hp1 | a0001 | c0002 | t0004 | g0284 | SAS | PJL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG03710 | hp2 | a0001 | c0002 | t0004 | g0037 | SAS | PJL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG03831 | hp1 | a0001 | c0002 | t0009 | g0123 | SAS | BEB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | BEB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG03834 | hp1 | a0001 | c0002 | t0004 | g0283 | SAS | BEB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG03942 | hp1 | a0001 | c0001 | t0048 | g0088 | SAS | BEB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | BEB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | STU | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG04115 | hp2 | a0001 | c0002 | t0071 | g0220 | SAS | STU | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0157 | SAS | BEB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG04184 | hp2 | a0001 | c0001 | t0006 | g0215 | SAS | BEB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | STU | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0282 | SAS | STU | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | STU | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18522 | hp1 | a0001 | c0002 | t0017 | g0024 | AFR | YRI | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18522 | hp2 | a0001 | c0002 | t0064 | g0243 | AFR | YRI | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | CHB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | CHB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18906 | hp1 | a0001 | c0002 | t0004 | g0309 | AFR | YRI | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18906 | hp2 | a0001 | c0002 | t0004 | g0168 | AFR | YRI | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18941 | hp1 | a0001 | c0001 | t0019 | g0274 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18942 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18942 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18945 | hp1 | a0001 | c0002 | t0011 | g0057 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18945 | hp2 | a0001 | c0001 | t0003 | g0145 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18947 | hp2 | a0001 | c0001 | t0003 | g0212 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18950 | hp1 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18951 | hp2 | a0001 | c0001 | t0005 | g0114 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18952 | hp1 | a0001 | c0001 | t0005 | g0328 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18953 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18954 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18954 | hp2 | a0001 | c0001 | t0005 | g0190 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18956 | hp2 | a0001 | c0001 | t0010 | g0028 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18957 | hp1 | a0001 | c0001 | t0019 | g0016 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18957 | hp2 | a0001 | c0001 | t0019 | g0122 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18959 | hp1 | a0001 | c0001 | t0005 | g0254 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18959 | hp2 | a0001 | c0002 | t0011 | g0208 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18960 | hp1 | a0001 | c0001 | t0008 | g0001 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18961 | hp1 | a0001 | c0001 | t0033 | g0289 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18961 | hp2 | a0001 | c0001 | t0058 | g0251 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18962 | hp1 | a0001 | c0002 | t0004 | g0255 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18962 | hp2 | a0001 | c0001 | t0006 | g0015 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18963 | hp1 | a0001 | c0002 | t0004 | g0217 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18963 | hp2 | a0001 | c0001 | t0049 | g0007 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18965 | hp2 | a0001 | c0002 | t0004 | g0090 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18966 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18966 | hp2 | a0001 | c0002 | t0011 | g0261 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18967 | hp2 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18970 | hp1 | a0001 | c0001 | t0008 | g0001 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18970 | hp2 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18971 | hp2 | a0001 | c0001 | t0005 | g0326 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18973 | hp2 | a0001 | c0002 | t0011 | g0245 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18974 | hp2 | a0001 | c0001 | t0010 | g0041 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18977 | hp2 | a0001 | c0001 | t0006 | g0197 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18978 | hp1 | a0001 | c0001 | t0005 | g0291 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18979 | hp1 | a0001 | c0001 | t0005 | g0036 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18980 | hp2 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18981 | hp1 | a0001 | c0001 | t0005 | g0315 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18981 | hp2 | a0001 | c0001 | t0030 | g0044 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18982 | hp1 | a0001 | c0001 | t0005 | g0058 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18985 | hp1 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18985 | hp2 | a0001 | c0002 | t0011 | g0247 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18986 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18986 | hp2 | a0001 | c0001 | t0045 | g0311 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18988 | hp1 | a0001 | c0002 | t0011 | g0029 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18988 | hp2 | a0001 | c0002 | t0004 | g0320 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18989 | hp1 | a0001 | c0002 | t0004 | g0266 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18990 | hp2 | a0001 | c0001 | t0008 | g0001 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18991 | hp1 | a0001 | c0002 | t0004 | g0324 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18991 | hp2 | a0001 | c0001 | t0005 | g0211 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18992 | hp2 | a0001 | c0001 | t0055 | g0006 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18993 | hp1 | a0001 | c0001 | t0010 | g0250 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18994 | hp2 | a0001 | c0002 | t0009 | g0198 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18995 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18998 | hp1 | a0001 | c0001 | t0044 | g0118 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19000 | hp2 | a0001 | c0002 | t0027 | g0290 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19001 | hp2 | a0001 | c0001 | t0005 | g0036 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19002 | hp1 | a0001 | c0001 | t0005 | g0072 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19002 | hp2 | a0001 | c0001 | t0003 | g0223 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19003 | hp2 | a0001 | c0001 | t0005 | g0234 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19004 | hp1 | a0001 | c0002 | t0004 | g0280 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19006 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19006 | hp2 | a0001 | c0001 | t0050 | g0056 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19007 | hp1 | a0001 | c0002 | t0004 | g0298 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19007 | hp2 | a0001 | c0001 | t0006 | g0015 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19009 | hp2 | a0001 | c0002 | t0004 | g0325 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19010 | hp2 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19011 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19012 | hp1 | a0001 | c0002 | t0004 | g0222 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19012 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19030 | hp1 | a0001 | c0002 | t0018 | g0023 | AFR | LWK | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19030 | hp2 | a0001 | c0001 | t0021 | g0134 | AFR | LWK | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19043 | hp1 | a0001 | c0001 | t0021 | g0313 | AFR | LWK | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19043 | hp2 | a0001 | c0002 | t0014 | g0150 | AFR | LWK | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19056 | hp1 | a0001 | c0005 | t0027 | g0119 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19056 | hp2 | a0001 | c0001 | t0043 | g0191 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19057 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19057 | hp2 | a0001 | c0002 | t0024 | g0262 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19058 | hp1 | a0001 | c0002 | t0024 | g0064 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19058 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19062 | hp1 | a0001 | c0001 | t0005 | g0303 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19062 | hp2 | a0001 | c0001 | t0008 | g0199 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19063 | hp1 | a0001 | c0001 | t0032 | g0004 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19065 | hp1 | a0001 | c0001 | t0008 | g0006 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19068 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19070 | hp1 | a0001 | c0002 | t0011 | g0029 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19070 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19072 | hp1 | a0001 | c0001 | t0003 | g0275 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19072 | hp2 | a0001 | c0001 | t0042 | g0005 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19074 | hp2 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19076 | hp1 | a0001 | c0001 | t0008 | g0330 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19077 | hp2 | a0001 | c0001 | t0054 | g0108 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19079 | hp2 | a0001 | c0001 | t0005 | g0105 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19080 | hp2 | a0001 | c0001 | t0046 | g0049 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19084 | hp1 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19086 | hp1 | a0001 | c0001 | t0041 | g0237 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19086 | hp2 | a0001 | c0001 | t0010 | g0028 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19087 | hp1 | a0001 | c0001 | t0010 | g0258 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19088 | hp2 | a0001 | c0001 | t0005 | g0304 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19090 | hp2 | a0001 | c0001 | t0035 | g0004 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19091 | hp1 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19240 | hp1 | a0001 | c0002 | t0015 | g0010 | AFR | YRI | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA19240 | hp2 | a0001 | c0001 | t0020 | g0132 | AFR | YRI | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA20129 | hp1 | a0001 | c0001 | t0006 | g0015 | AFR | ASW | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | ASW | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | TSI | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | TSI | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA20805 | hp1 | a0001 | c0001 | t0006 | g0244 | EUR | TSI | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0334 | EUR | TSI | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | GIH | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA20905 | hp2 | a0001 | c0001 | t0022 | g0005 | SAS | GIH | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01123 | hp1 | a0001 | c0002 | t0009 | g0301 | AMR | CLM | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02109 | hp1 | a0001 | c0002 | t0015 | g0010 | AFR | ACB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02109 | hp2 | a0001 | c0002 | t0036 | g0148 | AFR | ACB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02486 | hp1 | a0001 | c0001 | t0012 | g0031 | AFR | ACB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02486 | hp2 | a0001 | c0002 | t0007 | g0193 | AFR | ACB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02559 | hp1 | a0001 | c0002 | t0018 | g0023 | AFR | ACB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG02559 | hp2 | a0001 | c0002 | t0014 | g0341 | AFR | ACB | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG03471 | hp1 | a0001 | c0001 | t0005 | g0335 | AFR | MSL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG03471 | hp2 | a0001 | c0002 | t0007 | g0135 | AFR | MSL | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG06807 | hp1 | a0001 | c0002 | t0015 | g0172 | AFR | USA | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
HG06807 | hp2 | a0001 | c0002 | t0017 | g0024 | AFR | USA | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA20300 | hp1 | a0001 | c0001 | t0008 | g0214 | AFR | USA | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA20300 | hp2 | a0001 | c0001 | t0012 | g0176 | AFR | USA | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA21309 | hp1 | a0001 | c0001 | t0060 | g0156 | AFR | LWK | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
NA21309 | hp2 | a0001 | c0002 | t0007 | g0346 | AFR | LWK | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
homoSapiens | chm13v2 | a0001 | c0002 | t0075 | g0187 | REF | REF | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
homoSapiens | grch38p0 | a0001 | c0002 | t0065 | g0342 | REF | REF | TAF8_chr6_42045524_42088272 | TAF8 | chr6 | 42045524 | 42088272 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:42050559 | C | T | 1 | a0001c0005 | 1 | NA19056.hp1 | synonymous_variant | LOW | c.18C>T | p.Ala6Ala | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 1/9 | 36/6678 | 18/933 | 6/310 | chr6 | 42050559 | |||
chr6:42050574 | T | G | 1 | a0001c0003 | 1 | HG02922.hp1 | synonymous_variant | LOW | c.33T>G | p.Gly11Gly | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 1/9 | 51/6678 | 33/933 | 11/310 | chr6 | 42050574 | |||
chr6:42057513 | G | A | 1 | a0001c0004 | 1 | HG02055.hp2 | splice_region_variant&synonymous_variant | LOW | c.489G>A | p.Pro163Pro | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/9 | 507/6678 | 489/933 | 163/310 | chr6 | 42057513 | |||
chr6:42077207 | G | A | 3 | a0001c0001 a0001c0003 a0001c0004 |
334 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(331): Show |
synonymous_variant | LOW | c.888G>A | p.Arg296Arg | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 8/9 | 906/6678 | 888/933 | 296/310 | chr6 | 42077207 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:42077626 | G | A | 9 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0013 others(6): Show |
72 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*81G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 81 | chr6 | 42077626 | ||||||
chr6:42077633 | C | T | 1 | a0001c0001t0077 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*88C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 88 | chr6 | 42077633 | ||||||
chr6:42077758 | T | A | 9 | a0001c0002t0014 a0001c0002t0015 a0001c0002t0016 others(6): Show |
27 | HG01891.hp1 HG02109.hp1 HG02109.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*213T>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 213 | chr6 | 42077758 | ||||||
chr6:42077792 | A | G | 1 | a0001c0002t0039 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*247A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 247 | chr6 | 42077792 | ||||||
chr6:42077951 | TC | T | 1 | a0001c0001t0012 | 7 | HG00642.hp1 HG01891.hp2 HG02486.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*407delC | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 407 | chr6 | 42077951 | ||||||
chr6:42078233 | G | C | 1 | a0001c0002t0040 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*688G>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 688 | chr6 | 42078233 | ||||||
chr6:42078304 | G | A | 3 | a0001c0002t0011 a0001c0002t0024 a0001c0002t0040 |
10 | HG03688.hp2 NA18945.hp1 NA18959.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*759G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 759 | chr6 | 42078304 | ||||||
chr6:42078337 | A | T | 4 | a0001c0002t0009 a0001c0002t0029 a0001c0002t0074 others(1): Show |
14 | HG00280.hp2 HG01123.hp1 HG01169.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*792A>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 792 | chr6 | 42078337 | ||||||
chr6:42078341 | G | A | 54 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(51): Show |
363 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(360): Show |
3_prime_UTR_variant | MODIFIER | c.*796G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 796 | chr6 | 42078341 | ||||||
chr6:42078347 | CTG | C | 4 | a0001c0002t0009 a0001c0002t0029 a0001c0002t0074 others(1): Show |
14 | HG00280.hp2 HG01123.hp1 HG01169.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*804_*805delGT | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 804 | INFO_REALIGN_3_PRIME | chr6 | 42078347 | |||||
chr6:42078512 | C | T | 2 | a0001c0002t0028 a0001c0002t0073 |
3 | HG00741.hp1 HG02615.hp2 HG03491.hp1 |
3_prime_UTR_variant | MODIFIER | c.*967C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 967 | chr6 | 42078512 | ||||||
chr6:42078622 | C | G | 2 | a0001c0001t0022 a0001c0001t0063 |
4 | HG00733.hp1 HG01361.hp2 HG01981.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1077C>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 1077 | chr6 | 42078622 | ||||||
chr6:42078631 | G | C | 2 | a0001c0002t0017 a0001c0002t0036 |
5 | HG02109.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1086G>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 1086 | chr6 | 42078631 | ||||||
chr6:42078787 | A | G | 1 | a0001c0002t0072 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1242A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 1242 | chr6 | 42078787 | ||||||
chr6:42078845 | C | T | 1 | a0001c0001t0008 | 10 | HG01943.hp2 HG01952.hp2 HG02148.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1300C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 1300 | chr6 | 42078845 | ||||||
chr6:42078860 | G | A | 1 | a0001c0002t0023 | 2 | HG01891.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1315G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 1315 | chr6 | 42078860 | ||||||
chr6:42078919 | C | T | 13 | a0001c0001t0001 a0001c0002t0004 a0001c0002t0011 others(10): Show |
57 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*1374C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 1374 | chr6 | 42078919 | ||||||
chr6:42078949 | C | T | 11 | a0001c0001t0005 a0001c0001t0012 a0001c0001t0020 others(8): Show |
43 | HG00423.hp2 HG00438.hp1 HG00642.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*1404C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 1404 | chr6 | 42078949 | ||||||
chr6:42078950 | C | T | 11 | a0001c0001t0005 a0001c0001t0012 a0001c0001t0020 others(8): Show |
43 | HG00423.hp2 HG00438.hp1 HG00642.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*1405C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 1405 | chr6 | 42078950 | ||||||
chr6:42078978 | C | T | 11 | a0001c0002t0004 a0001c0002t0011 a0001c0002t0024 others(8): Show |
52 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*1433C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 1433 | chr6 | 42078978 | ||||||
chr6:42078979 | G | A | 1 | a0001c0002t0037 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1434G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 1434 | chr6 | 42078979 | ||||||
chr6:42079009 | C | T | 1 | a0001c0002t0067 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1464C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 1464 | chr6 | 42079009 | ||||||
chr6:42079110 | A | G | 1 | a0001c0002t0037 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1565A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 1565 | chr6 | 42079110 | ||||||
chr6:42079279 | G | A | 1 | a0001c0001t0056 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1734G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 1734 | chr6 | 42079279 | ||||||
chr6:42079433 | T | G | 1 | a0001c0001t0041 | 1 | NA19086.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1888T>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 1888 | chr6 | 42079433 | ||||||
chr6:42079568 | C | A | 1 | a0001c0002t0068 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2023C>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 2023 | chr6 | 42079568 | ||||||
chr6:42079656 | G | A | 1 | a0001c0001t0042 | 1 | NA19072.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2111G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 2111 | chr6 | 42079656 | ||||||
chr6:42079684 | G | T | 2 | a0001c0002t0017 a0001c0002t0036 |
5 | HG02109.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2139G>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 2139 | chr6 | 42079684 | ||||||
chr6:42079697 | C | T | 1 | a0001c0002t0066 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2152C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 2152 | chr6 | 42079697 | ||||||
chr6:42079715 | A | AT | 17 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0021 others(14): Show |
163 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(160): Show |
3_prime_UTR_variant | MODIFIER | c.*2188dupT | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 2189 | INFO_REALIGN_3_PRIME | chr6 | 42079715 | |||||
chr6:42079715 | AT | A | 12 | a0001c0001t0020 a0001c0001t0030 a0001c0001t0043 others(9): Show |
25 | HG01891.hp1 HG02145.hp1 HG02559.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*2188delT | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 2188 | INFO_REALIGN_3_PRIME | chr6 | 42079715 | |||||
chr6:42079741 | A | G | 8 | a0001c0002t0014 a0001c0002t0016 a0001c0002t0017 others(5): Show |
22 | HG01891.hp1 HG02109.hp2 HG02451.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2196A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 2196 | chr6 | 42079741 | ||||||
chr6:42079743 | G | A | 1 | a0001c0001t0056 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2198G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 2198 | chr6 | 42079743 | ||||||
chr6:42079834 | G | A | 8 | a0001c0002t0014 a0001c0002t0016 a0001c0002t0017 others(5): Show |
22 | HG01891.hp1 HG02109.hp2 HG02451.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2289G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 2289 | chr6 | 42079834 | ||||||
chr6:42079852 | C | T | 1 | a0001c0001t0055 | 1 | NA18992.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2307C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 2307 | chr6 | 42079852 | ||||||
chr6:42079904 | G | A | 1 | a0001c0002t0014 | 6 | HG02559.hp2 HG02647.hp1 HG02717.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2359G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 2359 | chr6 | 42079904 | ||||||
chr6:42079995 | T | TA | 17 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0008 others(14): Show |
202 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(199): Show |
3_prime_UTR_variant | MODIFIER | c.*2463dupA | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 2464 | INFO_REALIGN_3_PRIME | chr6 | 42079995 | |||||
chr6:42079995 | TA | T | 24 | a0001c0001t0045 a0001c0001t0049 a0001c0002t0004 others(21): Show |
80 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*2463delA | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 2463 | INFO_REALIGN_3_PRIME | chr6 | 42079995 | |||||
chr6:42080009 | T | A | 1 | a0001c0001t0050 | 1 | NA19006.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2464T>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 2464 | chr6 | 42080009 | ||||||
chr6:42080075 | C | T | 1 | a0001c0002t0018 | 4 | HG00741.hp2 HG02258.hp2 HG02559.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2530C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 2530 | chr6 | 42080075 | ||||||
chr6:42080095 | A | G | 1 | a0001c0001t0077 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2550A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 2550 | chr6 | 42080095 | ||||||
chr6:42080129 | A | G | 1 | a0001c0001t0062 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2584A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 2584 | chr6 | 42080129 | ||||||
chr6:42080131 | C | T | 2 | a0001c0002t0014 a0001c0002t0037 |
7 | HG02559.hp2 HG02647.hp1 HG02717.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2586C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 2586 | chr6 | 42080131 | ||||||
chr6:42080177 | C | T | 1 | a0001c0002t0029 | 2 | HG01934.hp2 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2632C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 2632 | chr6 | 42080177 | ||||||
chr6:42080256 | G | T | 13 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0019 others(10): Show |
158 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*2711G>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 2711 | chr6 | 42080256 | ||||||
chr6:42080308 | A | C | 2 | a0001c0002t0016 a0001c0002t0023 |
7 | HG01891.hp1 HG02976.hp2 HG03139.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2763A>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 2763 | chr6 | 42080308 | ||||||
chr6:42080372 | T | C | 1 | a0001c0002t0037 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2827T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 2827 | chr6 | 42080372 | ||||||
chr6:42080373 | C | CT | 3 | a0001c0002t0018 a0001c0002t0027 a0001c0005t0027 |
6 | HG00741.hp2 HG02258.hp2 HG02559.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2844dupT | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 2845 | INFO_REALIGN_3_PRIME | chr6 | 42080373 | |||||
chr6:42080376 | T | TTC | 2 | a0001c0002t0014 a0001c0002t0037 |
7 | HG02559.hp2 HG02647.hp1 HG02717.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2832_*2833insCT | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 2833 | INFO_REALIGN_3_PRIME | chr6 | 42080376 | |||||
chr6:42080377 | T | TC | 49 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(46): Show |
353 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(350): Show |
3_prime_UTR_variant | MODIFIER | c.*2832_*2833insC | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 2833 | chr6 | 42080377 | ||||||
chr6:42080378 | T | C | 2 | a0001c0001t0033 a0001c0001t0042 |
2 | NA18961.hp1 NA19072.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2833T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 2833 | chr6 | 42080378 | ||||||
chr6:42080418 | G | A | 1 | a0001c0001t0046 | 1 | NA19080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2873G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 2873 | chr6 | 42080418 | ||||||
chr6:42080596 | G | A | 1 | a0001c0002t0070 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3051G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 3051 | chr6 | 42080596 | ||||||
chr6:42080638 | T | C | 1 | a0001c0001t0057 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3093T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 3093 | chr6 | 42080638 | ||||||
chr6:42080844 | C | T | 1 | a0001c0002t0076 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3299C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 3299 | chr6 | 42080844 | ||||||
chr6:42080923 | A | G | 1 | a0001c0001t0061 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3378A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 3378 | chr6 | 42080923 | ||||||
chr6:42080952 | A | G | 36 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(33): Show |
195 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(192): Show |
3_prime_UTR_variant | MODIFIER | c.*3407A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 3407 | chr6 | 42080952 | ||||||
chr6:42081006 | A | G | 1 | a0001c0001t0062 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3461A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 3461 | chr6 | 42081006 | ||||||
chr6:42081048 | TAGAG | T | 2 | a0001c0002t0028 a0001c0002t0073 |
3 | HG00741.hp1 HG02615.hp2 HG03491.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3506_*3509delAGAG | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 3506 | INFO_REALIGN_3_PRIME | chr6 | 42081048 | |||||
chr6:42081054 | G | GCAAAATA others(36): Show |
1 | a0001c0001t0058 | 1 | NA18961.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3511_*3553dupAAAA others(39): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 3554 | INFO_REALIGN_3_PRIME | chr6 | 42081054 | |||||
chr6:42081105 | G | A | 52 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(49): Show |
361 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(358): Show |
3_prime_UTR_variant | MODIFIER | c.*3560G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 3560 | chr6 | 42081105 | ||||||
chr6:42081138 | C | G | 1 | a0001c0002t0018 | 4 | HG00741.hp2 HG02258.hp2 HG02559.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3593C>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 3593 | chr6 | 42081138 | ||||||
chr6:42081170 | A | AGT | 5 | a0001c0002t0007 a0001c0002t0015 a0001c0002t0028 others(2): Show |
11 | HG00741.hp1 HG02109.hp1 HG02615.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3645_*3646dupTG | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 3647 | INFO_REALIGN_3_PRIME | chr6 | 42081170 | |||||
chr6:42081170 | A | AGTGT | 10 | a0001c0001t0077 a0001c0002t0007 a0001c0002t0009 others(7): Show |
31 | HG00741.hp2 HG01169.hp1 HG01175.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*3643_*3646dupTGTG | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 3647 | INFO_REALIGN_3_PRIME | chr6 | 42081170 | |||||
chr6:42081170 | AGT | A | 1 | a0001c0001t0001 | 10 | HG00438.hp2 HG00544.hp2 HG02165.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3645_*3646delTG | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 3645 | INFO_REALIGN_3_PRIME | chr6 | 42081170 | |||||
chr6:42081170 | AGTGT | A | 12 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0019 others(9): Show |
143 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(140): Show |
3_prime_UTR_variant | MODIFIER | c.*3643_*3646delTGTG | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 3643 | INFO_REALIGN_3_PRIME | chr6 | 42081170 | |||||
chr6:42081170 | AGTGTGTG others(3): Show |
A | 2 | a0001c0001t0001 a0001c0001t0051 |
5 | HG00597.hp1 NA18952.hp2 NA18969.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3637_*3646delTGTG others(6): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 3637 | INFO_REALIGN_3_PRIME | chr6 | 42081170 | |||||
chr6:42081190 | T | TGTGC | 25 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(22): Show |
170 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(167): Show |
3_prime_UTR_variant | MODIFIER | c.*3646_*3647insTGCG | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 3647 | INFO_REALIGN_3_PRIME | chr6 | 42081190 | |||||
chr6:42081204 | T | C | 11 | a0001c0001t0005 a0001c0001t0012 a0001c0001t0020 others(8): Show |
43 | HG00423.hp2 HG00438.hp1 HG00642.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*3659T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 3659 | chr6 | 42081204 | ||||||
chr6:42081220 | G | A | 1 | a0001c0002t0074 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3675G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 3675 | chr6 | 42081220 | ||||||
chr6:42081221 | C | T | 1 | a0001c0001t0032 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3676C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 3676 | chr6 | 42081221 | ||||||
chr6:42081270 | G | A | 2 | a0001c0002t0016 a0001c0002t0023 |
7 | HG01891.hp1 HG02976.hp2 HG03139.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3725G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 3725 | chr6 | 42081270 | ||||||
chr6:42081325 | TACC | T | 24 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0019 others(21): Show |
188 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(185): Show |
3_prime_UTR_variant | MODIFIER | c.*3792_*3794delCAC | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 3792 | INFO_REALIGN_3_PRIME | chr6 | 42081325 | |||||
chr6:42081332 | A | T | 1 | a0001c0001t0053 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3787A>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 3787 | chr6 | 42081332 | ||||||
chr6:42081395 | G | A | 1 | a0001c0001t0031 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3850G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 3850 | chr6 | 42081395 | ||||||
chr6:42081445 | C | T | 23 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0019 others(20): Show |
186 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(183): Show |
3_prime_UTR_variant | MODIFIER | c.*3900C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 3900 | chr6 | 42081445 | ||||||
chr6:42081446 | G | A | 1 | a0001c0001t0060 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3901G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 3901 | chr6 | 42081446 | ||||||
chr6:42081454 | C | T | 1 | a0001c0002t0039 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3909C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 3909 | chr6 | 42081454 | ||||||
chr6:42081470 | G | A | 1 | a0001c0001t0051 | 1 | HG00597.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3925G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 3925 | chr6 | 42081470 | ||||||
chr6:42081525 | C | T | 2 | a0001c0002t0016 a0001c0002t0023 |
7 | HG01891.hp1 HG02976.hp2 HG03139.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3980C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 3980 | chr6 | 42081525 | ||||||
chr6:42081725 | T | C | 10 | a0001c0001t0043 a0001c0002t0007 a0001c0002t0009 others(7): Show |
35 | HG00280.hp2 HG00741.hp2 HG01123.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*4180T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 4180 | chr6 | 42081725 | ||||||
chr6:42081738 | C | T | 1 | a0001c0001t0013 | 6 | HG02717.hp1 HG02723.hp2 HG02886.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4193C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 4193 | chr6 | 42081738 | ||||||
chr6:42081797 | C | T | 16 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0019 others(13): Show |
166 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(163): Show |
3_prime_UTR_variant | MODIFIER | c.*4252C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 4252 | chr6 | 42081797 | ||||||
chr6:42081860 | T | G | 16 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0019 others(13): Show |
166 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(163): Show |
3_prime_UTR_variant | MODIFIER | c.*4315T>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 4315 | chr6 | 42081860 | ||||||
chr6:42081868 | C | T | 1 | a0001c0002t0073 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4323C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 4323 | chr6 | 42081868 | ||||||
chr6:42081869 | G | A | 2 | a0001c0002t0017 a0001c0002t0036 |
5 | HG02109.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4324G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 4324 | chr6 | 42081869 | ||||||
chr6:42082007 | T | C | 1 | a0001c0002t0039 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4462T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 4462 | chr6 | 42082007 | ||||||
chr6:42082045 | A | G | 1 | a0001c0001t0025 | 2 | HG03490.hp2 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4500A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 4500 | chr6 | 42082045 | ||||||
chr6:42082126 | C | T | 1 | a0001c0004t0052 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4581C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 4581 | chr6 | 42082126 | ||||||
chr6:42082162 | G | C | 23 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0019 others(20): Show |
186 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(183): Show |
3_prime_UTR_variant | MODIFIER | c.*4617G>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 4617 | chr6 | 42082162 | ||||||
chr6:42082428 | T | C | 1 | a0001c0002t0017 | 4 | HG02809.hp2 HG03139.hp1 HG06807.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4883T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 4883 | chr6 | 42082428 | ||||||
chr6:42082432 | G | A | 16 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0019 others(13): Show |
166 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(163): Show |
3_prime_UTR_variant | MODIFIER | c.*4887G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 4887 | chr6 | 42082432 | ||||||
chr6:42082478 | A | G | 3 | a0001c0002t0017 a0001c0002t0036 a0001c0002t0039 |
6 | HG02109.hp2 HG02622.hp1 HG02809.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4933A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 4933 | chr6 | 42082478 | ||||||
chr6:42082485 | T | C | 2 | a0001c0002t0016 a0001c0002t0023 |
7 | HG01891.hp1 HG02976.hp2 HG03139.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4940T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 4940 | chr6 | 42082485 | ||||||
chr6:42082621 | G | C | 8 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0013 others(5): Show |
71 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*5076G>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 5076 | chr6 | 42082621 | ||||||
chr6:42082632 | C | A | 1 | a0001c0001t0010 | 9 | HG00323.hp1 HG00621.hp1 HG02056.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*5087C>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 5087 | chr6 | 42082632 | ||||||
chr6:42082682 | T | C | 1 | a0001c0001t0056 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5137T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 5137 | chr6 | 42082682 | ||||||
chr6:42082692 | G | T | 1 | a0001c0004t0052 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5147G>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 5147 | chr6 | 42082692 | ||||||
chr6:42082882 | A | G | 51 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(48): Show |
360 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(357): Show |
3_prime_UTR_variant | MODIFIER | c.*5337A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 5337 | chr6 | 42082882 | ||||||
chr6:42082967 | T | C | 1 | a0001c0002t0037 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5422T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 5422 | chr6 | 42082967 | ||||||
chr6:42083085 | C | T | 8 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0013 others(5): Show |
71 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*5540C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 5540 | chr6 | 42083085 | ||||||
chr6:42083188 | A | C | 1 | a0001c0002t0039 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5643A>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 5643 | chr6 | 42083188 | ||||||
chr6:42083259 | T | C | 16 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0019 others(13): Show |
166 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(163): Show |
3_prime_UTR_variant | MODIFIER | c.*5714T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 9/9 | 5714 | chr6 | 42083259 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:42050611 | G | T | 1 | a0001c0001t0001g0347 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.45+25G>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 1/8 | chr6 | 42050611 | |||||||
chr6:42050683 | C | G | 1 | a0001c0002t0007g0346 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.45+97C>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 1/8 | chr6 | 42050683 | |||||||
chr6:42050794 | C | T | 3 | a0001c0001t0013g0344 a0001c0002t0007g0343 a0001c0002t0026g0345 |
3 | HG02723.hp2 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.45+208C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 1/8 | chr6 | 42050794 | |||||||
chr6:42050902 | T | G | 52 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0043 others(49): Show |
66 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.45+316T>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 1/8 | chr6 | 42050902 | |||||||
chr6:42050915 | T | G | 1 | a0001c0002t0007g0086 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.45+329T>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 1/8 | chr6 | 42050915 | |||||||
chr6:42051140 | T | C | 349 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(346): Show |
442 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(439): Show |
intron_variant | MODIFIER | c.46-217T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 1/8 | chr6 | 42051140 | |||||||
chr6:42051145 | G | T | 77 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0017 others(74): Show |
94 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.46-212G>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 1/8 | chr6 | 42051145 | |||||||
chr6:42051168 | T | G | 1 | a0001c0001t0010g0041 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.46-189T>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 1/8 | chr6 | 42051168 | |||||||
chr6:42051625 | G | A | 13 | a0001c0001t0001g0032 a0001c0001t0001g0282 a0001c0001t0001g0287 others(10): Show |
14 | HG00408.hp2 HG01975.hp2 HG01978.hp2 others(11): Show |
intron_variant | MODIFIER | c.202+112G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42051625 | |||||||
chr6:42051790 | G | A | 52 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0043 others(49): Show |
66 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.202+277G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42051790 | |||||||
chr6:42051834 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.202+321C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42051834 | |||||||
chr6:42051884 | T | G | 49 | a0001c0001t0001g0009 a0001c0001t0001g0091 a0001c0001t0001g0092 others(46): Show |
66 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.202+371T>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42051884 | |||||||
chr6:42052144 | G | GCTCACTT others(11): Show |
1 | a0001c0001t0001g0129 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.202+631_202+632ins others(18): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42052144 | |||||||
chr6:42052146 | G | C | 1 | a0001c0001t0001g0129 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.202+633G>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42052146 | |||||||
chr6:42052147 | A | T | 1 | a0001c0001t0001g0129 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.202+634A>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42052147 | |||||||
chr6:42052148 | G | C | 1 | a0001c0001t0001g0129 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.202+635G>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42052148 | |||||||
chr6:42052153 | A | G | 1 | a0001c0001t0003g0276 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.202+640A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42052153 | |||||||
chr6:42052317 | G | GC | 24 | a0001c0001t0001g0013 a0001c0001t0001g0043 a0001c0001t0001g0133 others(21): Show |
27 | HG00099.hp2 HG00408.hp1 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.202+815dupC | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 42052317 | ||||||
chr6:42052317 | GC | G | 132 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(129): Show |
170 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.202+815delC | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 42052317 | ||||||
chr6:42052318 | C | CG | 5 | a0001c0001t0012g0176 a0001c0001t0077g0170 a0001c0002t0007g0171 others(2): Show |
5 | HG02630.hp2 HG02895.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.202+805_202+806ins others(1): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42052318 | |||||||
chr6:42052328 | C | CTT | 9 | a0001c0001t0013g0147 a0001c0002t0004g0168 a0001c0002t0004g0177 others(6): Show |
9 | HG01891.hp1 HG02109.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.202+825_202+826dup others(2): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 42052328 | ||||||
chr6:42052558 | G | C | 2 | a0001c0001t0001g0033 a0001c0001t0005g0291 |
3 | HG00558.hp1 NA18978.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.202+1045G>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42052558 | |||||||
chr6:42052725 | T | G | 1 | a0001c0001t0003g0145 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.202+1212T>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42052725 | |||||||
chr6:42052727 | G | T | 1 | a0001c0001t0003g0145 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.202+1214G>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42052727 | |||||||
chr6:42052738 | G | T | 1 | a0001c0001t0003g0145 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.202+1225G>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42052738 | |||||||
chr6:42052802 | G | T | 1 | a0001c0001t0003g0145 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.202+1289G>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42052802 | |||||||
chr6:42052806 | G | T | 1 | a0001c0001t0003g0145 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.202+1293G>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42052806 | |||||||
chr6:42052814 | C | T | 60 | a0001c0001t0001g0001 a0001c0001t0001g0136 a0001c0001t0001g0138 others(57): Show |
80 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.202+1301C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42052814 | |||||||
chr6:42052829 | G | T | 1 | a0001c0001t0003g0145 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.202+1316G>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42052829 | |||||||
chr6:42052856 | G | A | 1 | a0001c0002t0007g0146 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.202+1343G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42052856 | |||||||
chr6:42052864 | T | A | 1 | a0001c0001t0003g0145 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.202+1351T>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42052864 | |||||||
chr6:42052865 | A | T | 1 | a0001c0001t0003g0145 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.202+1352A>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42052865 | |||||||
chr6:42052873 | C | G | 1 | a0001c0001t0003g0145 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.202+1360C>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42052873 | |||||||
chr6:42052878 | G | C | 1 | a0001c0001t0003g0145 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.202+1365G>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42052878 | |||||||
chr6:42052879 | G | A | 1 | a0001c0001t0003g0145 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.202+1366G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42052879 | |||||||
chr6:42052883 | A | G | 1 | a0001c0001t0003g0145 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.202+1370A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42052883 | |||||||
chr6:42052884 | T | G | 1 | a0001c0001t0003g0145 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.202+1371T>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42052884 | |||||||
chr6:42052885 | T | A | 1 | a0001c0001t0003g0145 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.202+1372T>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42052885 | |||||||
chr6:42052965 | G | A | 1 | a0001c0001t0003g0292 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.202+1452G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42052965 | |||||||
chr6:42053067 | C | T | 1 | a0001c0001t0001g0334 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.202+1554C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42053067 | |||||||
chr6:42053138 | G | T | 1 | a0001c0001t0059g0201 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.202+1625G>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42053138 | |||||||
chr6:42053328 | C | T | 8 | a0001c0001t0006g0271 a0001c0001t0012g0030 a0001c0001t0012g0031 others(5): Show |
10 | HG00642.hp1 HG01175.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.202+1815C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42053328 | |||||||
chr6:42053437 | C | T | 114 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(111): Show |
145 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.202+1924C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42053437 | |||||||
chr6:42053444 | A | G | 13 | a0001c0001t0012g0176 a0001c0001t0077g0170 a0001c0002t0004g0168 others(10): Show |
14 | HG01891.hp1 HG02257.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.202+1931A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42053444 | |||||||
chr6:42053565 | CA | C | 145 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0016 others(142): Show |
182 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.203-1953delA | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 42053565 | ||||||
chr6:42053565 | CAA | C | 48 | a0001c0001t0001g0009 a0001c0001t0001g0091 a0001c0001t0001g0092 others(45): Show |
64 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.203-1954_203-1953d others(4): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 42053565 | ||||||
chr6:42053565 | CAAAAAAA others(7): Show |
C | 8 | a0001c0001t0013g0161 a0001c0001t0056g0160 a0001c0001t0057g0163 others(5): Show |
8 | HG01081.hp2 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.203-1956_203-1943d others(16): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 42053565 | ||||||
chr6:42053583 | A | G | 1 | a0001c0001t0002g0022 | 2 | HG00558.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.203-1948A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42053583 | |||||||
chr6:42053618 | C | T | 58 | a0001c0001t0001g0001 a0001c0001t0001g0136 a0001c0001t0001g0138 others(55): Show |
78 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.203-1913C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42053618 | |||||||
chr6:42053638 | C | G | 1 | a0001c0002t0007g0086 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.203-1893C>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42053638 | |||||||
chr6:42053773 | G | C | 1 | a0001c0001t0001g0202 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.203-1758G>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42053773 | |||||||
chr6:42053801 | A | G | 61 | a0001c0001t0001g0001 a0001c0001t0001g0136 a0001c0001t0001g0138 others(58): Show |
81 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.203-1730A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42053801 | |||||||
chr6:42053959 | G | C | 1 | a0001c0002t0007g0146 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.203-1572G>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42053959 | |||||||
chr6:42054154 | T | C | 221 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(218): Show |
279 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.203-1377T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054154 | |||||||
chr6:42054175 | C | A | 1 | a0001c0001t0003g0145 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.203-1356C>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054175 | |||||||
chr6:42054176 | A | C | 1 | a0001c0001t0003g0145 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.203-1355A>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054176 | |||||||
chr6:42054178 | A | T | 1 | a0001c0001t0003g0145 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.203-1353A>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054178 | |||||||
chr6:42054180 | A | C | 1 | a0001c0001t0003g0145 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.203-1351A>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054180 | |||||||
chr6:42054181 | G | T | 1 | a0001c0001t0003g0145 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.203-1350G>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054181 | |||||||
chr6:42054192 | AAAACTCC others(7): Show |
A | 1 | a0001c0001t0003g0145 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.203-1334_203-1321d others(16): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 42054192 | ||||||
chr6:42054210 | C | T | 2 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
2 | HG00609.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.203-1321C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054210 | |||||||
chr6:42054214 | T | C | 358 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(355): Show |
451 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(448): Show |
intron_variant | MODIFIER | c.203-1317T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054214 | |||||||
chr6:42054218 | C | T | 1 | a0001c0001t0003g0145 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.203-1313C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054218 | |||||||
chr6:42054219 | T | A | 1 | a0001c0001t0003g0145 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.203-1312T>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054219 | |||||||
chr6:42054233 | T | C | 1 | a0001c0001t0003g0145 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.203-1298T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054233 | |||||||
chr6:42054238 | C | A | 1 | a0001c0001t0003g0145 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.203-1293C>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054238 | |||||||
chr6:42054243 | C | A | 1 | a0001c0001t0003g0145 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.203-1288C>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054243 | |||||||
chr6:42054250 | A | C | 1 | a0001c0001t0003g0145 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.203-1281A>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054250 | |||||||
chr6:42054265 | C | G | 1 | a0001c0001t0003g0145 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.203-1266C>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054265 | |||||||
chr6:42054266 | A | T | 1 | a0001c0001t0003g0145 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.203-1265A>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054266 | |||||||
chr6:42054273 | A | G | 1 | a0001c0001t0003g0145 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.203-1258A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054273 | |||||||
chr6:42054274 | G | C | 1 | a0001c0001t0003g0145 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.203-1257G>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054274 | |||||||
chr6:42054388 | G | A | 1 | a0001c0001t0003g0145 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.203-1143G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054388 | |||||||
chr6:42054390 | A | T | 1 | a0001c0001t0003g0145 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.203-1141A>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054390 | |||||||
chr6:42054391 | C | A | 1 | a0001c0001t0003g0145 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.203-1140C>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054391 | |||||||
chr6:42054493 | C | T | 6 | a0001c0001t0005g0335 a0001c0001t0013g0336 a0001c0001t0013g0338 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.203-1038C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054493 | |||||||
chr6:42054549 | G | A | 49 | a0001c0001t0001g0009 a0001c0001t0001g0091 a0001c0001t0001g0092 others(46): Show |
66 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.203-982G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054549 | |||||||
chr6:42054680 | CTCACTGC others(1): Show |
C | 6 | a0001c0001t0005g0154 a0001c0002t0009g0151 a0001c0002t0009g0153 others(3): Show |
6 | HG01255.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.203-850_203-843del others(8): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054680 | |||||||
chr6:42054692 | A | T | 6 | a0001c0001t0005g0154 a0001c0002t0009g0151 a0001c0002t0009g0153 others(3): Show |
6 | HG01255.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.203-839A>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054692 | |||||||
chr6:42054696 | C | G | 6 | a0001c0001t0005g0154 a0001c0002t0009g0151 a0001c0002t0009g0153 others(3): Show |
6 | HG01255.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.203-835C>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054696 | |||||||
chr6:42054697 | C | CTTGA | 6 | a0001c0001t0005g0154 a0001c0002t0009g0151 a0001c0002t0009g0153 others(3): Show |
6 | HG01255.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.203-834_203-833ins others(4): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054697 | |||||||
chr6:42054739 | G | C | 1 | a0001c0001t0001g0047 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.203-792G>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054739 | |||||||
chr6:42054806 | A | G | 8 | a0001c0001t0013g0161 a0001c0001t0056g0160 a0001c0001t0057g0163 others(5): Show |
8 | HG01081.hp2 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.203-725A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054806 | |||||||
chr6:42054825 | T | C | 49 | a0001c0001t0001g0009 a0001c0001t0001g0091 a0001c0001t0001g0092 others(46): Show |
66 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.203-706T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054825 | |||||||
chr6:42054904 | C | T | 2 | a0001c0001t0044g0118 a0001c0005t0027g0119 |
2 | NA18998.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.203-627C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42054904 | |||||||
chr6:42054931 | C | CT | 9 | a0001c0001t0001g0084 a0001c0001t0013g0161 a0001c0001t0056g0160 others(6): Show |
9 | HG01081.hp2 HG02258.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.203-585dupT | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 42054931 | ||||||
chr6:42054931 | CT | C | 51 | a0001c0001t0001g0009 a0001c0001t0001g0091 a0001c0001t0001g0092 others(48): Show |
68 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.203-585delT | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 42054931 | ||||||
chr6:42055077 | C | T | 49 | a0001c0001t0001g0009 a0001c0001t0001g0091 a0001c0001t0001g0092 others(46): Show |
66 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.203-454C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42055077 | |||||||
chr6:42055128 | T | C | 9 | a0001c0001t0013g0147 a0001c0002t0004g0168 a0001c0002t0004g0177 others(6): Show |
10 | HG01891.hp1 HG02109.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.203-403T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42055128 | |||||||
chr6:42055207 | C | T | 49 | a0001c0001t0001g0009 a0001c0001t0001g0091 a0001c0001t0001g0092 others(46): Show |
66 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.203-324C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42055207 | |||||||
chr6:42055215 | C | T | 1 | a0001c0001t0005g0333 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.203-316C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42055215 | |||||||
chr6:42055361 | G | A | 349 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(346): Show |
442 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(439): Show |
intron_variant | MODIFIER | c.203-170G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42055361 | |||||||
chr6:42055373 | G | A | 9 | a0001c0001t0013g0147 a0001c0002t0004g0168 a0001c0002t0004g0177 others(6): Show |
10 | HG01891.hp1 HG02109.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.203-158G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 2/8 | chr6 | 42055373 | |||||||
chr6:42055783 | A | G | 78 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0017 others(75): Show |
95 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.301+154A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 3/8 | chr6 | 42055783 | |||||||
chr6:42055880 | A | ATAC | 49 | a0001c0001t0001g0009 a0001c0001t0001g0091 a0001c0001t0001g0092 others(46): Show |
66 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.302-63_302-61dupCT others(1): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr6 | 42055880 | ||||||
chr6:42056071 | AAGTAATT others(4): Show |
A | 1 | a0001c0002t0004g0288 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.364+59_364+69delGT others(9): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr6 | 42056071 | ||||||
chr6:42056239 | T | A | 8 | a0001c0001t0006g0271 a0001c0001t0012g0030 a0001c0001t0012g0031 others(5): Show |
10 | HG00642.hp1 HG01175.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.364+225T>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 4/8 | chr6 | 42056239 | |||||||
chr6:42056401 | A | G | 12 | a0001c0001t0001g0124 a0001c0001t0001g0127 a0001c0001t0002g0007 others(9): Show |
18 | HG00423.hp1 HG00558.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.364+387A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 4/8 | chr6 | 42056401 | |||||||
chr6:42056491 | C | T | 1 | a0001c0002t0004g0266 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.364+477C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 4/8 | chr6 | 42056491 | |||||||
chr6:42056547 | G | A | 49 | a0001c0001t0001g0009 a0001c0001t0001g0091 a0001c0001t0001g0092 others(46): Show |
66 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.364+533G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 4/8 | chr6 | 42056547 | |||||||
chr6:42056552 | GAGT | G | 7 | a0001c0001t0012g0176 a0001c0001t0077g0170 a0001c0002t0007g0171 others(4): Show |
7 | HG02257.hp2 HG02630.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.364+540_364+542del others(3): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr6 | 42056552 | ||||||
chr6:42056558 | C | T | 2 | a0001c0001t0020g0331 a0001c0001t0020g0332 |
2 | HG02145.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.364+544C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 4/8 | chr6 | 42056558 | |||||||
chr6:42056633 | C | T | 1 | a0001c0001t0002g0116 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.364+619C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 4/8 | chr6 | 42056633 | |||||||
chr6:42056688 | C | T | 1 | a0001c0003t0047g0273 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.364+674C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 4/8 | chr6 | 42056688 | |||||||
chr6:42056754 | C | T | 1 | a0001c0001t0059g0201 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.365-635C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 4/8 | chr6 | 42056754 | |||||||
chr6:42056858 | G | A | 3 | a0001c0001t0013g0344 a0001c0002t0007g0343 a0001c0002t0026g0345 |
3 | HG02723.hp2 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.365-531G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 4/8 | chr6 | 42056858 | |||||||
chr6:42056867 | G | A | 281 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(278): Show |
357 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(354): Show |
intron_variant | MODIFIER | c.365-522G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 4/8 | chr6 | 42056867 | |||||||
chr6:42056896 | G | A | 49 | a0001c0001t0001g0009 a0001c0001t0001g0091 a0001c0001t0001g0092 others(46): Show |
66 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.365-493G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 4/8 | chr6 | 42056896 | |||||||
chr6:42056902 | G | A | 8 | a0001c0001t0006g0271 a0001c0001t0012g0030 a0001c0001t0012g0031 others(5): Show |
10 | HG00642.hp1 HG01175.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.365-487G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 4/8 | chr6 | 42056902 | |||||||
chr6:42057051 | G | A | 1 | a0001c0001t0005g0333 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.365-338G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 4/8 | chr6 | 42057051 | |||||||
chr6:42057123 | G | A | 1 | a0001c0002t0007g0146 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.365-266G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 4/8 | chr6 | 42057123 | |||||||
chr6:42057305 | G | C | 1 | a0001c0001t0003g0120 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.365-84G>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 4/8 | chr6 | 42057305 | |||||||
chr6:42057320 | G | A | 138 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(135): Show |
174 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.365-69G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 4/8 | chr6 | 42057320 | |||||||
chr6:42057537 | G | A | 1 | a0001c0002t0018g0155 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.489+24G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42057537 | |||||||
chr6:42057580 | G | A | 49 | a0001c0001t0001g0009 a0001c0001t0001g0091 a0001c0001t0001g0092 others(46): Show |
66 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.489+67G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42057580 | |||||||
chr6:42057664 | A | G | 141 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(138): Show |
183 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.489+151A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42057664 | |||||||
chr6:42057772 | T | G | 2 | a0001c0001t0001g0085 a0001c0001t0003g0048 |
2 | HG00673.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.489+259T>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42057772 | |||||||
chr6:42057776 | G | GA | 279 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(276): Show |
355 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(352): Show |
intron_variant | MODIFIER | c.489+273dupA | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 42057776 | ||||||
chr6:42057807 | A | C | 62 | a0001c0001t0001g0009 a0001c0001t0001g0091 a0001c0001t0001g0092 others(59): Show |
80 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.489+294A>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42057807 | |||||||
chr6:42057855 | G | A | 3 | a0001c0001t0012g0030 a0001c0001t0012g0031 a0001c0001t0012g0267 |
5 | HG00642.hp1 HG02486.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.489+342G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42057855 | |||||||
chr6:42057967 | T | C | 8 | a0001c0001t0013g0161 a0001c0001t0056g0160 a0001c0001t0057g0163 others(5): Show |
8 | HG01081.hp2 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.489+454T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42057967 | |||||||
chr6:42058147 | G | T | 7 | a0001c0001t0012g0176 a0001c0001t0077g0170 a0001c0002t0007g0171 others(4): Show |
7 | HG02257.hp2 HG02630.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.489+634G>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42058147 | |||||||
chr6:42058254 | C | T | 1 | a0001c0002t0017g0165 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.489+741C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42058254 | |||||||
chr6:42058255 | A | G | 281 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(278): Show |
357 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(354): Show |
intron_variant | MODIFIER | c.489+742A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42058255 | |||||||
chr6:42058306 | G | T | 12 | a0001c0001t0001g0124 a0001c0001t0001g0127 a0001c0001t0002g0007 others(9): Show |
18 | HG00423.hp1 HG00558.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.489+793G>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42058306 | |||||||
chr6:42058389 | T | G | 2 | a0001c0001t0002g0042 a0001c0001t0046g0049 |
2 | HG02135.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.489+876T>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42058389 | |||||||
chr6:42058452 | G | A | 58 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0133 others(55): Show |
72 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.489+939G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42058452 | |||||||
chr6:42058467 | T | C | 1 | a0001c0002t0015g0010 | 5 | HG02109.hp1 HG02976.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.489+954T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42058467 | |||||||
chr6:42058544 | TC | T | 3 | a0001c0001t0005g0178 a0001c0001t0006g0025 a0001c0002t0066g0200 |
4 | HG02145.hp2 HG02257.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+1033delC | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 42058544 | ||||||
chr6:42058748 | C | G | 1 | a0001c0002t0068g0115 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.489+1235C>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42058748 | |||||||
chr6:42058764 | C | G | 151 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(148): Show |
186 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.489+1251C>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42058764 | |||||||
chr6:42058978 | T | A | 1 | a0001c0002t0014g0149 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.489+1465T>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42058978 | |||||||
chr6:42059043 | G | C | 4 | a0001c0001t0056g0160 a0001c0002t0007g0158 a0001c0002t0007g0159 others(1): Show |
4 | HG01081.hp2 HG02258.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.489+1530G>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42059043 | |||||||
chr6:42059341 | C | T | 5 | a0001c0001t0006g0271 a0001c0002t0009g0270 a0001c0002t0029g0268 others(2): Show |
5 | HG01175.hp2 HG01243.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.489+1828C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42059341 | |||||||
chr6:42059361 | C | G | 1 | a0001c0001t0001g0233 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.489+1848C>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42059361 | |||||||
chr6:42059386 | A | G | 8 | a0001c0001t0006g0271 a0001c0001t0012g0030 a0001c0001t0012g0031 others(5): Show |
10 | HG00642.hp1 HG01175.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.489+1873A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42059386 | |||||||
chr6:42059390 | A | C | 49 | a0001c0001t0001g0009 a0001c0001t0001g0091 a0001c0001t0001g0092 others(46): Show |
66 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.489+1877A>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42059390 | |||||||
chr6:42059391 | A | G | 2 | a0001c0001t0006g0025 a0001c0002t0066g0200 |
3 | HG02145.hp2 HG02257.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.489+1878A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42059391 | |||||||
chr6:42059632 | A | G | 2 | a0001c0001t0001g0144 a0001c0001t0001g0232 |
2 | HG01261.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.489+2119A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42059632 | |||||||
chr6:42059983 | G | A | 1 | a0001c0001t0019g0274 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.489+2470G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42059983 | |||||||
chr6:42059992 | G | A | 2 | a0001c0002t0028g0182 a0001c0002t0028g0183 |
2 | HG00741.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.489+2479G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42059992 | |||||||
chr6:42060162 | A | G | 1 | a0001c0002t0017g0264 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.489+2649A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42060162 | |||||||
chr6:42060177 | A | C | 2 | a0001c0001t0002g0012 a0001c0001t0005g0114 |
4 | NA18951.hp2 NA18975.hp1 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+2664A>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42060177 | |||||||
chr6:42060200 | A | G | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(222): Show |
284 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.489+2687A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42060200 | |||||||
chr6:42060307 | T | G | 1 | a0001c0001t0001g0179 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.489+2794T>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42060307 | |||||||
chr6:42060492 | G | A | 37 | a0001c0001t0001g0009 a0001c0001t0001g0091 a0001c0001t0001g0092 others(34): Show |
48 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.489+2979G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42060492 | |||||||
chr6:42060834 | T | C | 12 | a0001c0001t0001g0043 a0001c0001t0001g0051 a0001c0001t0001g0052 others(9): Show |
12 | HG00673.hp2 NA18945.hp1 NA18952.hp2 others(9): Show |
intron_variant | MODIFIER | c.489+3321T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42060834 | |||||||
chr6:42061020 | G | A | 1 | a0001c0001t0063g0184 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.489+3507G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42061020 | |||||||
chr6:42061025 | A | T | 8 | a0001c0001t0005g0335 a0001c0001t0013g0336 a0001c0001t0013g0338 others(5): Show |
8 | HG02280.hp1 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.489+3512A>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42061025 | |||||||
chr6:42061058 | A | G | 1 | a0001c0002t0007g0346 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.489+3545A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42061058 | |||||||
chr6:42061385 | T | C | 3 | a0001c0001t0013g0344 a0001c0002t0007g0343 a0001c0002t0026g0345 |
3 | HG02723.hp2 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.489+3872T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42061385 | |||||||
chr6:42061502 | C | T | 1 | a0001c0001t0012g0267 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.489+3989C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42061502 | |||||||
chr6:42061533 | C | A | 49 | a0001c0001t0001g0009 a0001c0001t0001g0091 a0001c0001t0001g0092 others(46): Show |
66 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.489+4020C>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42061533 | |||||||
chr6:42061724 | A | T | 5 | a0001c0001t0001g0009 a0001c0001t0001g0113 a0001c0001t0002g0112 others(2): Show |
9 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(6): Show |
intron_variant | MODIFIER | c.489+4211A>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42061724 | |||||||
chr6:42061734 | A | G | 1 | a0001c0001t0059g0201 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.489+4221A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42061734 | |||||||
chr6:42061791 | C | T | 5 | a0001c0001t0006g0271 a0001c0002t0009g0270 a0001c0002t0029g0268 others(2): Show |
5 | HG01175.hp2 HG01243.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.489+4278C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42061791 | |||||||
chr6:42061843 | AGTTTGTC others(11): Show |
A | 11 | a0001c0001t0005g0335 a0001c0001t0013g0336 a0001c0001t0013g0338 others(8): Show |
11 | HG02280.hp1 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.489+4335_489+4352d others(20): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 42061843 | ||||||
chr6:42061904 | A | G | 64 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0133 others(61): Show |
86 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.489+4391A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42061904 | |||||||
chr6:42061950 | G | A | 281 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(278): Show |
357 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(354): Show |
intron_variant | MODIFIER | c.490-4362G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42061950 | |||||||
chr6:42062084 | G | GA | 8 | a0001c0001t0006g0271 a0001c0001t0012g0030 a0001c0001t0012g0031 others(5): Show |
10 | HG00642.hp1 HG01175.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.490-4224dupA | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 42062084 | ||||||
chr6:42062128 | A | G | 49 | a0001c0001t0001g0009 a0001c0001t0001g0091 a0001c0001t0001g0092 others(46): Show |
66 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.490-4184A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42062128 | |||||||
chr6:42062167 | C | T | 133 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(130): Show |
166 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.490-4145C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42062167 | |||||||
chr6:42062168 | G | A | 49 | a0001c0001t0001g0009 a0001c0001t0001g0091 a0001c0001t0001g0092 others(46): Show |
66 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.490-4144G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42062168 | |||||||
chr6:42062529 | C | CT | 49 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0018 others(46): Show |
60 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.490-3759dupT | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 42062529 | ||||||
chr6:42062529 | C | CTT | 88 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0027 others(85): Show |
115 | HG00642.hp1 HG00735.hp2 HG00741.hp1 others(112): Show |
intron_variant | MODIFIER | c.490-3760_490-3759d others(4): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 42062529 | ||||||
chr6:42062529 | C | CTTT | 62 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0047 others(59): Show |
77 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.490-3761_490-3759d others(5): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 42062529 | ||||||
chr6:42062529 | C | CTTTT | 6 | a0001c0001t0001g0043 a0001c0001t0001g0083 a0001c0001t0003g0080 others(3): Show |
6 | HG00544.hp1 HG00621.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.490-3762_490-3759d others(6): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 42062529 | ||||||
chr6:42062529 | CT | C | 56 | a0001c0001t0001g0009 a0001c0001t0001g0091 a0001c0001t0001g0092 others(53): Show |
73 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.490-3759delT | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 42062529 | ||||||
chr6:42062730 | T | C | 281 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(278): Show |
357 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(354): Show |
intron_variant | MODIFIER | c.490-3582T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42062730 | |||||||
chr6:42062731 | G | A | 1 | a0001c0002t0007g0265 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.490-3581G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42062731 | |||||||
chr6:42062742 | A | G | 9 | a0001c0001t0001g0127 a0001c0001t0013g0161 a0001c0001t0056g0160 others(6): Show |
9 | HG01081.hp2 HG02258.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.490-3570A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42062742 | |||||||
chr6:42062846 | ATCTTTAA others(5): Show |
A | 1 | a0001c0001t0001g0240 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.490-3462_490-3451d others(14): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 42062846 | ||||||
chr6:42062907 | G | T | 37 | a0001c0001t0001g0009 a0001c0001t0001g0091 a0001c0001t0001g0092 others(34): Show |
48 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.490-3405G>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42062907 | |||||||
chr6:42063003 | C | G | 1 | a0001c0001t0002g0228 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.490-3309C>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42063003 | |||||||
chr6:42063108 | G | C | 1 | a0001c0001t0002g0206 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.490-3204G>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42063108 | |||||||
chr6:42063122 | C | T | 8 | a0001c0001t0006g0271 a0001c0001t0012g0030 a0001c0001t0012g0031 others(5): Show |
10 | HG00642.hp1 HG01175.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.490-3190C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42063122 | |||||||
chr6:42063140 | C | G | 49 | a0001c0001t0001g0009 a0001c0001t0001g0091 a0001c0001t0001g0092 others(46): Show |
66 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.490-3172C>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42063140 | |||||||
chr6:42063287 | C | A | 1 | a0001c0001t0048g0088 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.490-3025C>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42063287 | |||||||
chr6:42063360 | G | A | 281 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(278): Show |
357 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(354): Show |
intron_variant | MODIFIER | c.490-2952G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42063360 | |||||||
chr6:42063509 | T | C | 2 | a0001c0001t0013g0295 a0001c0002t0007g0034 |
3 | HG02896.hp2 HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.490-2803T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42063509 | |||||||
chr6:42064219 | C | G | 2 | a0001c0001t0001g0226 a0001c0001t0001g0227 |
2 | NA19010.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.490-2093C>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42064219 | |||||||
chr6:42064251 | T | G | 1 | a0001c0001t0030g0044 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.490-2061T>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42064251 | |||||||
chr6:42064255 | G | GT | 56 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0043 others(53): Show |
70 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.490-2050dupT | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 42064255 | ||||||
chr6:42064255 | G | T | 1 | a0001c0001t0030g0044 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.490-2057G>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42064255 | |||||||
chr6:42064322 | G | A | 8 | a0001c0001t0013g0161 a0001c0001t0056g0160 a0001c0001t0057g0163 others(5): Show |
8 | HG01081.hp2 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.490-1990G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42064322 | |||||||
chr6:42064362 | C | T | 1 | a0001c0001t0001g0239 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.490-1950C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42064362 | |||||||
chr6:42064378 | C | A | 6 | a0001c0002t0004g0168 a0001c0002t0004g0177 a0001c0002t0017g0024 others(3): Show |
7 | HG01891.hp1 HG03139.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.490-1934C>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42064378 | |||||||
chr6:42064443 | C | A | 86 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0017 others(83): Show |
103 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.490-1869C>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42064443 | |||||||
chr6:42064634 | C | T | 1 | a0001c0001t0021g0313 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.490-1678C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42064634 | |||||||
chr6:42064754 | G | A | 1 | a0001c0002t0007g0146 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.490-1558G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42064754 | |||||||
chr6:42064830 | G | A | 2 | a0001c0001t0001g0226 a0001c0001t0001g0227 |
2 | NA19010.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.490-1482G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42064830 | |||||||
chr6:42064872 | G | C | 2 | a0001c0001t0001g0207 a0001c0002t0011g0208 |
2 | NA18959.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.490-1440G>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42064872 | |||||||
chr6:42064881 | CGGGGGGC others(3): Show |
C | 267 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(264): Show |
342 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(339): Show |
intron_variant | MODIFIER | c.490-1429_490-1420d others(12): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 42064881 | ||||||
chr6:42064894 | T | C | 267 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(264): Show |
342 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(339): Show |
intron_variant | MODIFIER | c.490-1418T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42064894 | |||||||
chr6:42064895 | TG | T | 267 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(264): Show |
342 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(339): Show |
intron_variant | MODIFIER | c.490-1416delG | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42064895 | |||||||
chr6:42064898 | AGTGAG | A | 267 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(264): Show |
342 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(339): Show |
intron_variant | MODIFIER | c.490-1413_490-1409d others(7): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42064898 | |||||||
chr6:42064913 | C | T | 1 | a0001c0002t0004g0312 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.490-1399C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42064913 | |||||||
chr6:42064914 | G | A | 57 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0133 others(54): Show |
71 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.490-1398G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42064914 | |||||||
chr6:42064914 | G | T | 2 | a0001c0002t0004g0059 a0001c0002t0004g0079 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.490-1398G>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42064914 | |||||||
chr6:42064956 | C | CA | 56 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0027 others(53): Show |
78 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.490-1334dupA | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 42064956 | ||||||
chr6:42064956 | C | CAAA | 7 | a0001c0001t0013g0161 a0001c0001t0056g0160 a0001c0001t0057g0163 others(4): Show |
7 | HG01081.hp2 HG02258.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.490-1336_490-1334d others(5): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 42064956 | ||||||
chr6:42064956 | CA | C | 69 | a0001c0001t0001g0009 a0001c0001t0001g0075 a0001c0001t0001g0078 others(66): Show |
87 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.490-1334delA | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 42064956 | ||||||
chr6:42064956 | CAA | C | 64 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0107 others(61): Show |
80 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.490-1335_490-1334d others(4): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 42064956 | ||||||
chr6:42065071 | C | G | 1 | a0001c0001t0002g0116 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.490-1241C>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42065071 | |||||||
chr6:42065170 | A | G | 1 | a0001c0001t0005g0058 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.490-1142A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42065170 | |||||||
chr6:42065241 | G | T | 2 | a0001c0002t0007g0346 a0001c0002t0015g0010 |
6 | HG02109.hp1 HG02976.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.490-1071G>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42065241 | |||||||
chr6:42065311 | A | T | 3 | a0001c0001t0005g0178 a0001c0001t0006g0025 a0001c0002t0066g0200 |
4 | HG02145.hp2 HG02257.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-1001A>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42065311 | |||||||
chr6:42065331 | G | A | 126 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(123): Show |
168 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.490-981G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42065331 | |||||||
chr6:42065442 | A | G | 57 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0133 others(54): Show |
71 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.490-870A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42065442 | |||||||
chr6:42065538 | A | G | 2 | a0001c0001t0013g0147 a0001c0002t0036g0148 |
2 | HG02109.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.490-774A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42065538 | |||||||
chr6:42065697 | C | T | 1 | a0001c0001t0003g0046 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.490-615C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42065697 | |||||||
chr6:42065702 | C | T | 140 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(137): Show |
174 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.490-610C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42065702 | |||||||
chr6:42065898 | T | A | 4 | a0001c0001t0001g0075 a0001c0002t0004g0059 a0001c0002t0004g0076 others(1): Show |
4 | HG00323.hp2 HG01123.hp2 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-414T>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42065898 | |||||||
chr6:42065938 | C | T | 2 | a0001c0001t0001g0207 a0001c0002t0011g0208 |
2 | NA18959.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.490-374C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42065938 | |||||||
chr6:42066060 | C | T | 1 | a0001c0002t0009g0194 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.490-252C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42066060 | |||||||
chr6:42066149 | C | G | 1 | a0001c0001t0005g0328 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.490-163C>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42066149 | |||||||
chr6:42066308 | G | A | 1 | a0001c0002t0024g0064 | 1 | NA19058.hp1 | splice_region_variant&intron_variant | LOW | c.490-4G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 5/8 | chr6 | 42066308 | |||||||
chr6:42066670 | C | G | 1 | a0001c0002t0017g0264 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.637+211C>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 6/8 | chr6 | 42066670 | |||||||
chr6:42066671 | T | C | 267 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(264): Show |
342 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(339): Show |
intron_variant | MODIFIER | c.637+212T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 6/8 | chr6 | 42066671 | |||||||
chr6:42066795 | C | T | 2 | a0001c0002t0007g0346 a0001c0002t0015g0010 |
6 | HG02109.hp1 HG02976.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.637+336C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 6/8 | chr6 | 42066795 | |||||||
chr6:42066917 | C | T | 6 | a0001c0001t0005g0154 a0001c0002t0009g0151 a0001c0002t0009g0153 others(3): Show |
6 | HG01255.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.637+458C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 6/8 | chr6 | 42066917 | |||||||
chr6:42066934 | C | T | 12 | a0001c0001t0001g0124 a0001c0001t0001g0127 a0001c0001t0002g0007 others(9): Show |
18 | HG00423.hp1 HG00558.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.637+475C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 6/8 | chr6 | 42066934 | |||||||
chr6:42066947 | C | T | 210 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(207): Show |
268 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.637+488C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 6/8 | chr6 | 42066947 | |||||||
chr6:42067312 | G | A | 8 | a0001c0001t0013g0161 a0001c0001t0056g0160 a0001c0001t0057g0163 others(5): Show |
8 | HG01081.hp2 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.637+853G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 6/8 | chr6 | 42067312 | |||||||
chr6:42067326 | C | G | 1 | a0001c0001t0001g0078 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.637+867C>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 6/8 | chr6 | 42067326 | |||||||
chr6:42067370 | C | T | 1 | a0001c0001t0012g0176 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.637+911C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 6/8 | chr6 | 42067370 | |||||||
chr6:42067499 | G | C | 6 | a0001c0001t0013g0161 a0001c0001t0056g0160 a0001c0001t0057g0163 others(3): Show |
6 | HG01081.hp2 HG02572.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.638-966G>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 6/8 | chr6 | 42067499 | |||||||
chr6:42067521 | A | G | 1 | a0001c0001t0006g0074 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.638-944A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 6/8 | chr6 | 42067521 | |||||||
chr6:42067856 | C | T | 1 | a0001c0001t0001g0327 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.638-609C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 6/8 | chr6 | 42067856 | |||||||
chr6:42068189 | T | C | 267 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(264): Show |
342 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(339): Show |
intron_variant | MODIFIER | c.638-276T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 6/8 | chr6 | 42068189 | |||||||
chr6:42068322 | G | A | 1 | a0001c0001t0002g0228 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.638-143G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 6/8 | chr6 | 42068322 | |||||||
chr6:42068331 | T | C | 6 | a0001c0001t0020g0132 a0001c0001t0060g0156 a0001c0002t0016g0131 others(3): Show |
7 | HG00741.hp2 HG02258.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.638-134T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 6/8 | chr6 | 42068331 | |||||||
chr6:42068461 | C | T | 1 | a0001c0001t0005g0326 | 1 | NA18971.hp2 | splice_region_variant&intron_variant | LOW | c.638-4C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 6/8 | chr6 | 42068461 | |||||||
chr6:42068657 | A | C | 275 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(272): Show |
350 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(347): Show |
intron_variant | MODIFIER | c.780+50A>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42068657 | |||||||
chr6:42068706 | C | T | 8 | a0001c0001t0006g0271 a0001c0001t0012g0030 a0001c0001t0012g0031 others(5): Show |
10 | HG00642.hp1 HG01175.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.780+99C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42068706 | |||||||
chr6:42068767 | A | G | 7 | a0001c0001t0012g0176 a0001c0001t0077g0170 a0001c0002t0007g0171 others(4): Show |
7 | HG02257.hp2 HG02630.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.780+160A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42068767 | |||||||
chr6:42068909 | G | A | 3 | a0001c0002t0004g0278 a0001c0002t0004g0286 a0001c0002t0004g0288 |
3 | HG01975.hp2 HG01978.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.780+302G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42068909 | |||||||
chr6:42069011 | A | G | 8 | a0001c0001t0006g0271 a0001c0001t0012g0030 a0001c0001t0012g0031 others(5): Show |
10 | HG00642.hp1 HG01175.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.780+404A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42069011 | |||||||
chr6:42069062 | CCT | C | 8 | a0001c0001t0013g0161 a0001c0001t0056g0160 a0001c0001t0057g0163 others(5): Show |
8 | HG01081.hp2 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.780+456_780+457del others(2): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42069062 | |||||||
chr6:42069084 | T | C | 1 | a0001c0001t0005g0333 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.780+477T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42069084 | |||||||
chr6:42069112 | G | T | 63 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0133 others(60): Show |
77 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.780+505G>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42069112 | |||||||
chr6:42069352 | A | G | 1 | a0001c0001t0034g0297 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.780+745A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42069352 | |||||||
chr6:42069360 | T | G | 152 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(149): Show |
194 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.780+753T>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42069360 | |||||||
chr6:42069369 | G | A | 1 | a0001c0002t0004g0298 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.780+762G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42069369 | |||||||
chr6:42069429 | C | T | 57 | a0001c0001t0001g0009 a0001c0001t0001g0091 a0001c0001t0001g0092 others(54): Show |
76 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.780+822C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42069429 | |||||||
chr6:42069439 | G | C | 1 | a0001c0001t0020g0332 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.780+832G>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42069439 | |||||||
chr6:42069604 | T | C | 11 | a0001c0001t0001g0009 a0001c0001t0001g0091 a0001c0001t0001g0092 others(8): Show |
15 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(12): Show |
intron_variant | MODIFIER | c.780+997T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42069604 | |||||||
chr6:42069610 | T | C | 49 | a0001c0001t0001g0009 a0001c0001t0001g0091 a0001c0001t0001g0092 others(46): Show |
66 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.780+1003T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42069610 | |||||||
chr6:42069725 | G | A | 1 | a0001c0001t0001g0213 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.780+1118G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42069725 | |||||||
chr6:42069890 | C | G | 57 | a0001c0001t0001g0009 a0001c0001t0001g0091 a0001c0001t0001g0092 others(54): Show |
76 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.780+1283C>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42069890 | |||||||
chr6:42069944 | A | C | 2 | a0001c0001t0001g0225 a0001c0001t0001g0233 |
2 | HG02040.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.780+1337A>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42069944 | |||||||
chr6:42069977 | C | T | 1 | a0001c0001t0059g0201 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.780+1370C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42069977 | |||||||
chr6:42069982 | A | G | 2 | a0001c0001t0063g0184 a0001c0002t0007g0146 |
2 | HG01981.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.780+1375A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42069982 | |||||||
chr6:42070214 | C | T | 5 | a0001c0001t0006g0271 a0001c0002t0009g0270 a0001c0002t0029g0268 others(2): Show |
5 | HG01175.hp2 HG01243.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.780+1607C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42070214 | |||||||
chr6:42070293 | C | T | 1 | a0001c0001t0002g0126 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.780+1686C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42070293 | |||||||
chr6:42070332 | C | CA | 143 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(140): Show |
182 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.780+1735dupA | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 42070332 | ||||||
chr6:42070340 | A | C | 48 | a0001c0001t0001g0009 a0001c0001t0001g0091 a0001c0001t0001g0092 others(45): Show |
65 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.780+1733A>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42070340 | |||||||
chr6:42070392 | C | T | 1 | a0001c0001t0005g0211 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.780+1785C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42070392 | |||||||
chr6:42070407 | G | T | 8 | a0001c0001t0006g0271 a0001c0001t0012g0030 a0001c0001t0012g0031 others(5): Show |
10 | HG00642.hp1 HG01175.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.780+1800G>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42070407 | |||||||
chr6:42070433 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.780+1826C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42070433 | |||||||
chr6:42070447 | G | A | 1 | a0001c0001t0003g0317 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.780+1840G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42070447 | |||||||
chr6:42070690 | A | G | 12 | a0001c0001t0013g0147 a0001c0001t0013g0161 a0001c0001t0013g0344 others(9): Show |
12 | HG01081.hp2 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.780+2083A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42070690 | |||||||
chr6:42070711 | C | T | 65 | a0001c0001t0001g0009 a0001c0001t0001g0033 a0001c0001t0001g0092 others(62): Show |
83 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.780+2104C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42070711 | |||||||
chr6:42070964 | T | G | 2 | a0001c0002t0018g0023 a0001c0002t0018g0130 |
3 | HG02258.hp2 HG02559.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.780+2357T>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42070964 | |||||||
chr6:42070983 | C | G | 75 | a0001c0001t0001g0006 a0001c0001t0001g0033 a0001c0001t0001g0084 others(72): Show |
89 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.780+2376C>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42070983 | |||||||
chr6:42071029 | C | T | 12 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0078 others(9): Show |
16 | HG00639.hp1 HG01070.hp2 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.780+2422C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42071029 | |||||||
chr6:42071127 | T | C | 10 | a0001c0001t0006g0025 a0001c0001t0013g0336 a0001c0001t0013g0344 others(7): Show |
11 | HG02257.hp1 HG02451.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.780+2520T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42071127 | |||||||
chr6:42071187 | G | A | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(249): Show |
338 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.780+2580G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42071187 | |||||||
chr6:42071230 | T | C | 1 | a0001c0002t0039g0339 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.780+2623T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42071230 | |||||||
chr6:42071249 | G | A | 1 | a0001c0002t0029g0268 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.780+2642G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42071249 | |||||||
chr6:42071311 | C | CT | 26 | a0001c0001t0002g0063 a0001c0001t0002g0096 a0001c0001t0002g0157 others(23): Show |
27 | HG00408.hp2 HG00597.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.780+2737dupT | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 42071311 | ||||||
chr6:42071311 | C | CTT | 10 | a0001c0001t0005g0291 a0001c0001t0005g0321 a0001c0001t0010g0028 others(7): Show |
11 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(8): Show |
intron_variant | MODIFIER | c.780+2736_780+2737d others(4): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 42071311 | ||||||
chr6:42071311 | C | CTTTT | 8 | a0001c0001t0005g0154 a0001c0001t0061g0281 a0001c0002t0009g0153 others(5): Show |
8 | HG01255.hp1 HG02559.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.780+2734_780+2737d others(6): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 42071311 | ||||||
chr6:42071311 | CT | C | 32 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0001g0294 others(29): Show |
44 | HG00673.hp1 HG00673.hp2 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.780+2737delT | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 42071311 | ||||||
chr6:42071311 | CTT | C | 15 | a0001c0001t0001g0302 a0001c0001t0002g0143 a0001c0001t0003g0050 others(12): Show |
15 | HG01123.hp1 HG01175.hp2 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.780+2736_780+2737d others(4): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 42071311 | ||||||
chr6:42071311 | CTTT | C | 30 | a0001c0001t0001g0104 a0001c0001t0002g0067 a0001c0001t0002g0089 others(27): Show |
31 | HG00280.hp2 HG00733.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.780+2735_780+2737d others(5): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 42071311 | ||||||
chr6:42071311 | CTTTTTTT others(7): Show |
C | 5 | a0001c0001t0001g0084 a0001c0001t0001g0323 a0001c0001t0003g0205 others(2): Show |
5 | HG02735.hp1 NA18949.hp2 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.780+2724_780+2737d others(16): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 42071311 | ||||||
chr6:42071311 | CTTTTTTT others(8): Show |
C | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(137): Show |
202 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.780+2723_780+2737d others(17): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 42071311 | ||||||
chr6:42071311 | CTTTTTTT others(9): Show |
C | 2 | a0001c0001t0001g0226 a0001c0001t0006g0318 |
2 | HG03669.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.780+2722_780+2737d others(18): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 42071311 | ||||||
chr6:42071311 | CTTTTTTT others(13): Show |
C | 6 | a0001c0001t0001g0033 a0001c0001t0001g0065 a0001c0001t0001g0235 others(3): Show |
15 | HG00558.hp1 HG00735.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.780+2718_780+2737d others(22): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 42071311 | ||||||
chr6:42071342 | T | G | 1 | a0001c0003t0047g0273 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.780+2735T>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42071342 | |||||||
chr6:42071344 | T | A | 26 | a0001c0001t0001g0033 a0001c0001t0001g0065 a0001c0001t0001g0104 others(23): Show |
35 | HG00558.hp1 HG00733.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.780+2737T>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42071344 | |||||||
chr6:42071359 | T | A | 2 | a0001c0002t0018g0023 a0001c0002t0018g0130 |
3 | HG02258.hp2 HG02559.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.780+2752T>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42071359 | |||||||
chr6:42071394 | T | C | 47 | a0001c0001t0001g0035 a0001c0001t0001g0052 a0001c0001t0001g0054 others(44): Show |
55 | HG00323.hp1 HG00544.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.780+2787T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42071394 | |||||||
chr6:42071412 | G | A | 1 | a0001c0002t0073g0257 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.780+2805G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42071412 | |||||||
chr6:42071475 | A | G | 13 | a0001c0001t0002g0007 a0001c0001t0002g0022 a0001c0001t0002g0042 others(10): Show |
19 | HG00423.hp1 HG00558.hp2 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.780+2868A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42071475 | |||||||
chr6:42071487 | G | A | 1 | a0001c0001t0003g0292 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.780+2880G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42071487 | |||||||
chr6:42071488 | G | T | 2 | a0001c0001t0006g0025 a0001c0002t0004g0038 |
4 | HG00099.hp1 HG02257.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.780+2881G>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42071488 | |||||||
chr6:42071515 | G | A | 16 | a0001c0001t0013g0161 a0001c0001t0034g0297 a0001c0001t0051g0296 others(13): Show |
16 | HG00280.hp2 HG00597.hp1 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.780+2908G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42071515 | |||||||
chr6:42071526 | G | A | 297 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(294): Show |
384 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(381): Show |
intron_variant | MODIFIER | c.780+2919G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42071526 | |||||||
chr6:42071537 | G | A | 3 | a0001c0002t0028g0182 a0001c0002t0028g0183 a0001c0002t0073g0257 |
3 | HG00741.hp1 HG02615.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.780+2930G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42071537 | |||||||
chr6:42071626 | G | A | 4 | a0001c0001t0021g0306 a0001c0001t0021g0313 a0001c0001t0056g0160 others(1): Show |
4 | HG01081.hp2 HG01884.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.780+3019G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42071626 | |||||||
chr6:42071639 | T | C | 3 | a0001c0002t0026g0137 a0001c0002t0026g0345 a0001c0002t0037g0166 |
3 | HG02451.hp1 HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.780+3032T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42071639 | |||||||
chr6:42071749 | T | C | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(162): Show |
223 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(220): Show |
intron_variant | MODIFIER | c.780+3142T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42071749 | |||||||
chr6:42071762 | A | G | 3 | a0001c0001t0013g0147 a0001c0001t0013g0336 a0001c0001t0013g0344 |
3 | HG02723.hp2 HG02922.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.780+3155A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42071762 | |||||||
chr6:42071774 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.780+3167G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42071774 | |||||||
chr6:42071801 | C | A | 2 | a0001c0001t0021g0306 a0001c0001t0021g0313 |
2 | HG01884.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.780+3194C>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42071801 | |||||||
chr6:42071804 | G | A | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(97): Show |
146 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.780+3197G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42071804 | |||||||
chr6:42071813 | C | T | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(103): Show |
152 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.780+3206C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42071813 | |||||||
chr6:42071834 | A | G | 38 | a0001c0001t0001g0192 a0001c0001t0005g0036 a0001c0001t0005g0058 others(35): Show |
41 | HG00423.hp2 HG00438.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.780+3227A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42071834 | |||||||
chr6:42071928 | C | T | 302 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(299): Show |
389 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(386): Show |
intron_variant | MODIFIER | c.780+3321C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42071928 | |||||||
chr6:42072060 | G | A | 1 | a0001c0001t0062g0340 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.780+3453G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42072060 | |||||||
chr6:42072077 | C | T | 4 | a0001c0001t0021g0306 a0001c0001t0021g0313 a0001c0001t0056g0160 others(1): Show |
4 | HG01081.hp2 HG01884.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.780+3470C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42072077 | |||||||
chr6:42072139 | G | A | 1 | a0001c0001t0005g0253 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.780+3532G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42072139 | |||||||
chr6:42072145 | C | T | 306 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(303): Show |
394 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(391): Show |
intron_variant | MODIFIER | c.780+3538C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42072145 | |||||||
chr6:42072222 | A | C | 1 | a0001c0001t0001g0248 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.780+3615A>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42072222 | |||||||
chr6:42072288 | A | G | 90 | a0001c0001t0001g0104 a0001c0001t0001g0192 a0001c0001t0002g0003 others(87): Show |
111 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.780+3681A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42072288 | |||||||
chr6:42072404 | CCCTGT | C | 4 | a0001c0002t0007g0193 a0001c0002t0007g0263 a0001c0002t0007g0265 others(1): Show |
4 | HG02280.hp1 HG02486.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.780+3798_780+3802d others(7): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42072404 | |||||||
chr6:42072492 | T | G | 1 | a0001c0001t0008g0330 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.780+3885T>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42072492 | |||||||
chr6:42072553 | C | T | 44 | a0001c0001t0001g0104 a0001c0001t0002g0003 a0001c0001t0002g0007 others(41): Show |
61 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.780+3946C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42072553 | |||||||
chr6:42072583 | G | A | 110 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(107): Show |
157 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(154): Show |
intron_variant | MODIFIER | c.780+3976G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42072583 | |||||||
chr6:42072587 | C | T | 1 | a0001c0002t0004g0309 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.780+3980C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42072587 | |||||||
chr6:42072648 | C | T | 1 | a0001c0001t0001g0260 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.780+4041C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42072648 | |||||||
chr6:42072729 | G | GT | 10 | a0001c0001t0005g0036 a0001c0001t0005g0190 a0001c0001t0010g0258 others(7): Show |
12 | HG01169.hp1 HG02109.hp2 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.780+4133dupT | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 42072729 | ||||||
chr6:42072783 | C | T | 4 | a0001c0002t0017g0024 a0001c0002t0017g0165 a0001c0002t0017g0264 others(1): Show |
5 | HG02109.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.780+4176C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42072783 | |||||||
chr6:42072848 | C | G | 6 | a0001c0001t0002g0099 a0001c0001t0013g0161 a0001c0002t0007g0135 others(3): Show |
6 | HG00733.hp2 HG02717.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.780+4241C>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42072848 | |||||||
chr6:42072851 | C | T | 1 | a0001c0001t0002g0099 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.780+4244C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42072851 | |||||||
chr6:42072856 | A | G | 1 | a0001c0001t0002g0099 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.781-4244A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42072856 | |||||||
chr6:42072863 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.781-4237C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42072863 | |||||||
chr6:42072868 | G | A | 46 | a0001c0001t0001g0104 a0001c0001t0002g0003 a0001c0001t0002g0007 others(43): Show |
63 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.781-4232G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42072868 | |||||||
chr6:42072880 | G | T | 3 | a0001c0002t0015g0010 a0001c0002t0015g0172 a0001c0003t0047g0273 |
7 | HG02109.hp1 HG02922.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.781-4220G>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42072880 | |||||||
chr6:42072884 | G | C | 1 | a0001c0001t0008g0330 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.781-4216G>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42072884 | |||||||
chr6:42072891 | T | G | 1 | a0001c0002t0004g0283 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.781-4209T>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42072891 | |||||||
chr6:42072953 | G | A | 45 | a0001c0001t0001g0104 a0001c0001t0002g0003 a0001c0001t0002g0007 others(42): Show |
62 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.781-4147G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42072953 | |||||||
chr6:42072978 | C | T | 4 | a0001c0001t0021g0306 a0001c0001t0021g0313 a0001c0001t0056g0160 others(1): Show |
4 | HG01081.hp2 HG01884.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.781-4122C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42072978 | |||||||
chr6:42073002 | C | G | 83 | a0001c0001t0001g0104 a0001c0001t0001g0192 a0001c0001t0002g0003 others(80): Show |
103 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.781-4098C>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42073002 | |||||||
chr6:42073214 | C | G | 1 | a0001c0001t0001g0139 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.781-3886C>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42073214 | |||||||
chr6:42073214 | C | T | 1 | a0001c0001t0021g0134 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.781-3886C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42073214 | |||||||
chr6:42073333 | G | A | 1 | a0001c0002t0004g0298 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.781-3767G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42073333 | |||||||
chr6:42073437 | G | A | 1 | a0001c0001t0019g0274 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.781-3663G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42073437 | |||||||
chr6:42073488 | G | T | 1 | a0001c0002t0007g0346 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.781-3612G>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42073488 | |||||||
chr6:42073536 | G | A | 1 | a0001c0003t0047g0273 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.781-3564G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42073536 | |||||||
chr6:42073708 | G | A | 17 | a0001c0001t0005g0335 a0001c0001t0013g0147 a0001c0001t0013g0161 others(14): Show |
17 | HG02559.hp2 HG02622.hp2 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.781-3392G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42073708 | |||||||
chr6:42073778 | G | C | 1 | a0001c0002t0039g0339 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.781-3322G>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42073778 | |||||||
chr6:42073800 | G | A | 2 | a0001c0002t0026g0137 a0001c0002t0026g0345 |
2 | HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.781-3300G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42073800 | |||||||
chr6:42073803 | C | T | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(222): Show |
293 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(290): Show |
intron_variant | MODIFIER | c.781-3297C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42073803 | |||||||
chr6:42073862 | G | C | 1 | a0001c0002t0066g0200 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.781-3238G>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42073862 | |||||||
chr6:42074097 | G | C | 1 | a0001c0001t0034g0297 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.781-3003G>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42074097 | |||||||
chr6:42074205 | G | A | 2 | a0001c0001t0001g0293 a0001c0001t0001g0319 |
2 | HG02523.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.781-2895G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42074205 | |||||||
chr6:42074225 | G | A | 4 | a0001c0001t0013g0147 a0001c0001t0013g0336 a0001c0001t0013g0344 others(1): Show |
4 | HG02145.hp2 HG02723.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.781-2875G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42074225 | |||||||
chr6:42074297 | C | T | 12 | a0001c0001t0043g0191 a0001c0002t0009g0188 a0001c0002t0009g0189 others(9): Show |
12 | HG00280.hp2 HG01123.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.781-2803C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42074297 | |||||||
chr6:42074827 | C | T | 3 | a0001c0002t0007g0135 a0001c0002t0007g0346 a0001c0002t0064g0243 |
3 | HG03471.hp2 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.781-2273C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42074827 | |||||||
chr6:42074838 | CT | C | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(162): Show |
230 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.781-2244delT | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 42074838 | ||||||
chr6:42074838 | CTT | C | 55 | a0001c0001t0001g0293 a0001c0001t0005g0335 a0001c0001t0013g0147 others(52): Show |
57 | HG00280.hp2 HG00741.hp2 HG01081.hp2 others(54): Show |
intron_variant | MODIFIER | c.781-2245_781-2244d others(4): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 42074838 | ||||||
chr6:42074838 | CTTT | C | 45 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0012 others(42): Show |
62 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.781-2246_781-2244d others(5): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 42074838 | ||||||
chr6:42075074 | T | C | 2 | a0001c0002t0007g0034 a0001c0002t0007g0171 |
3 | HG02895.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.781-2026T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42075074 | |||||||
chr6:42075148 | A | G | 11 | a0001c0002t0009g0151 a0001c0002t0009g0153 a0001c0002t0009g0188 others(8): Show |
11 | HG00280.hp2 HG01123.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.781-1952A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42075148 | |||||||
chr6:42075182 | A | G | 1 | a0001c0002t0009g0189 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.781-1918A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42075182 | |||||||
chr6:42075262 | G | A | 1 | a0001c0002t0016g0173 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.781-1838G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42075262 | |||||||
chr6:42075327 | G | A | 6 | a0001c0002t0016g0131 a0001c0002t0016g0173 a0001c0002t0016g0174 others(3): Show |
6 | HG01891.hp1 HG02257.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.781-1773G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42075327 | |||||||
chr6:42075395 | A | G | 5 | a0001c0001t0005g0036 a0001c0001t0005g0190 a0001c0001t0005g0304 others(2): Show |
6 | NA18954.hp2 NA18961.hp2 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.781-1705A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42075395 | |||||||
chr6:42075419 | C | T | 1 | a0001c0002t0004g0288 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.781-1681C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42075419 | |||||||
chr6:42075526 | G | A | 33 | a0001c0001t0002g0003 a0001c0001t0002g0012 a0001c0001t0002g0063 others(30): Show |
44 | HG00323.hp1 HG00621.hp1 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.781-1574G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42075526 | |||||||
chr6:42075656 | GACTTCTT others(12): Show |
G | 1 | a0001c0003t0047g0273 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.781-1432_781-1414d others(21): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 42075656 | ||||||
chr6:42075664 | C | G | 81 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0012 others(78): Show |
100 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.781-1436C>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42075664 | |||||||
chr6:42075706 | C | T | 1 | a0001c0002t0004g0298 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.781-1394C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42075706 | |||||||
chr6:42075772 | A | T | 31 | a0001c0001t0043g0191 a0001c0002t0007g0034 a0001c0002t0007g0086 others(28): Show |
33 | HG00280.hp2 HG00741.hp2 HG01123.hp1 others(30): Show |
intron_variant | MODIFIER | c.781-1328A>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42075772 | |||||||
chr6:42075858 | T | C | 1 | a0001c0001t0005g0105 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.781-1242T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42075858 | |||||||
chr6:42076001 | AGAT | A | 7 | a0001c0001t0005g0335 a0001c0001t0013g0147 a0001c0001t0013g0161 others(4): Show |
7 | HG02717.hp1 HG02723.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.781-1098_781-1096d others(5): Show |
TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42076001 | |||||||
chr6:42076036 | C | T | 1 | a0001c0002t0011g0247 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.781-1064C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42076036 | |||||||
chr6:42076037 | G | A | 2 | a0001c0001t0003g0046 a0001c0001t0003g0094 |
2 | HG02083.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.781-1063G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42076037 | |||||||
chr6:42076206 | C | CA | 9 | a0001c0001t0013g0344 a0001c0002t0016g0131 a0001c0002t0016g0162 others(6): Show |
9 | HG01891.hp1 HG02257.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.781-882dupA | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 42076206 | ||||||
chr6:42076279 | G | A | 2 | a0001c0001t0001g0144 a0001c0001t0001g0232 |
2 | HG01261.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.781-821G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42076279 | |||||||
chr6:42076306 | C | T | 1 | a0001c0001t0008g0214 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.781-794C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42076306 | |||||||
chr6:42076375 | C | T | 3 | a0001c0001t0001g0210 a0001c0001t0001g0221 a0001c0001t0077g0170 |
3 | HG02630.hp2 HG03704.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.781-725C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42076375 | |||||||
chr6:42076399 | G | A | 1 | a0001c0003t0047g0273 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.781-701G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42076399 | |||||||
chr6:42076451 | A | G | 3 | a0001c0001t0020g0132 a0001c0001t0020g0331 a0001c0001t0020g0332 |
3 | HG02145.hp1 HG02572.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.781-649A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42076451 | |||||||
chr6:42076466 | A | C | 60 | a0001c0001t0003g0004 a0001c0001t0003g0008 a0001c0001t0003g0021 others(57): Show |
74 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.781-634A>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42076466 | |||||||
chr6:42076493 | G | C | 2 | a0001c0001t0005g0253 a0001c0001t0059g0201 |
2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.781-607G>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42076493 | |||||||
chr6:42076535 | C | T | 46 | a0001c0001t0005g0036 a0001c0001t0005g0058 a0001c0001t0005g0072 others(43): Show |
50 | HG00423.hp2 HG00438.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.781-565C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42076535 | |||||||
chr6:42076681 | G | T | 1 | a0001c0001t0050g0056 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.781-419G>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42076681 | |||||||
chr6:42076682 | C | G | 1 | a0001c0001t0050g0056 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.781-418C>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42076682 | |||||||
chr6:42076683 | G | C | 1 | a0001c0001t0050g0056 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.781-417G>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42076683 | |||||||
chr6:42076793 | G | C | 1 | a0001c0001t0001g0180 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.781-307G>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42076793 | |||||||
chr6:42076867 | T | C | 8 | a0001c0002t0016g0131 a0001c0002t0016g0162 a0001c0002t0016g0164 others(5): Show |
8 | HG01891.hp1 HG02257.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.781-233T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42076867 | |||||||
chr6:42076877 | G | A | 6 | a0001c0001t0013g0147 a0001c0001t0013g0161 a0001c0001t0013g0295 others(3): Show |
6 | HG02717.hp1 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.781-223G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42076877 | |||||||
chr6:42076880 | G | A | 6 | a0001c0001t0013g0147 a0001c0001t0013g0161 a0001c0001t0013g0295 others(3): Show |
6 | HG02717.hp1 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.781-220G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42076880 | |||||||
chr6:42076915 | T | C | 2 | a0001c0002t0004g0280 a0001c0002t0072g0285 |
2 | HG00408.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.781-185T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42076915 | |||||||
chr6:42076917 | C | G | 44 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0012 others(41): Show |
61 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.781-183C>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42076917 | |||||||
chr6:42077009 | A | G | 1 | a0001c0002t0007g0086 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.781-91A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42077009 | |||||||
chr6:42077087 | C | T | 4 | a0001c0002t0017g0024 a0001c0002t0017g0165 a0001c0002t0017g0264 others(1): Show |
5 | HG02109.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.781-13C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 7/8 | chr6 | 42077087 | |||||||
chr6:42077288 | G | A | 34 | a0001c0002t0007g0034 a0001c0002t0007g0086 a0001c0002t0007g0135 others(31): Show |
36 | HG00280.hp2 HG00741.hp1 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.920+49G>A | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 8/8 | chr6 | 42077288 | |||||||
chr6:42077292 | T | C | 1 | a0001c0002t0007g0086 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.920+53T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 8/8 | chr6 | 42077292 | |||||||
chr6:42077325 | G | T | 1 | a0001c0002t0014g0149 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.920+86G>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 8/8 | chr6 | 42077325 | |||||||
chr6:42077348 | C | T | 11 | a0001c0002t0009g0151 a0001c0002t0009g0153 a0001c0002t0009g0188 others(8): Show |
11 | HG00280.hp2 HG01123.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.920+109C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 8/8 | chr6 | 42077348 | |||||||
chr6:42077367 | T | C | 1 | a0001c0001t0001g0323 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.920+128T>C | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 8/8 | chr6 | 42077367 | |||||||
chr6:42077368 | C | T | 1 | a0001c0001t0001g0323 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.920+129C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 8/8 | chr6 | 42077368 | |||||||
chr6:42077433 | A | G | 35 | a0001c0001t0043g0191 a0001c0002t0007g0034 a0001c0002t0007g0086 others(32): Show |
37 | HG00280.hp2 HG00741.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.921-100A>G | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 8/8 | chr6 | 42077433 | |||||||
chr6:42077496 | C | T | 1 | a0001c0001t0008g0214 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.921-37C>T | TAF8 | ENSG00000137413.17 | transcript | ENST00000372977.8 | protein_coding | 8/8 | chr6 | 42077496 |