Search by Gene
| Item | Value |
|---|---|
| geneid | 6883 |
| ensemblid | ENSG00000120656.14 |
| hgncid | 11545 |
| symbol | TAF12 |
| name | TATA-box binding protein associated factor 12 |
| refseq_nuc | NM_005644.4 |
| refseq_prot | NP_005635.1 |
| ensembl_nuc | ENST00000373824.9 |
| ensembl_prot | ENSP00000362930.4 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 28602850 |
| end | 28643067 |
| strand | - |
| ver | v1.2 |
| region | chr1:28602850-28643067 |
| region5000 | chr1:28597850-28648067 |
| regionname0 | TAF12_chr1_28602850_28643067 |
| regionname5000 | TAF12_chr1_28597850_28648067 |
Multiple Alignments (by translate haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
Multiple Alignments (by aa haplotype frequency)
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 483 | 300 | 82 | 66 | 96 | 16 | 40 | TAF12_chr1_28597850_28648067 | TAF12 | ATGAA others(478): Show |
chr1 | 28597850 | 28648067 |
| acthapid | grch38/chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1335 | 290 | 75 | 63 | 96 | 16 | 40 | TAF12_chr1_28597850_28648067 | TAF12 | AGTCG others(1330): Show |
chr1 | 28597850 | 28648067 |
| a0001c0001t0002 | 0/0 | 1333 | 8 | 6 | 2 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | AGTCG others(1328): Show |
chr1 | 28597850 | 28648067 |
| a0001c0001t0003 | 0/0 | 1335 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | AGTCG others(1330): Show |
chr1 | 28597850 | 28648067 |
| a0001c0001t0004 | 0/0 | 1335 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | AGTCG others(1330): Show |
chr1 | 28597850 | 28648067 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0002g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0002g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0003g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| a0001c0001t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0054 | EUR | GBR | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0205 | EUR | GBR | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0233 | EUR | GBR | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0101 | EUR | GBR | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0235 | EUR | FIN | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0207 | EUR | FIN | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | CHS | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | CHS | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | CHS | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | CHS | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | CHS | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | CHS | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | CLM | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | CLM | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | CLM | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | CLM | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | CLM | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0245 | EUR | IBS | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0017 | EUR | IBS | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0262 | EUR | IBS | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0169 | EUR | IBS | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0260 | EUR | IBS | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0142 | EUR | IBS | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | ACB | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | PEL | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | PEL | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | PEL | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | ACB | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | KHV | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0178 | AFR | ACB | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | ACB | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | PEL | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | CDX | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | CDX | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | CDX | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | CDX | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | ACB | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | PEL | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PEL | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PEL | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | GWD | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | GWD | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | GWD | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | GWD | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | GWD | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | GWD | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | ESN | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ESN | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | ESN | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | GWD | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | MSL | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | MSL | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | ESN | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | ESN | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ESN | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | ESN | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ESN | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | MSL | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | MSL | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | MSL | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | MSL | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | MSL | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | MSL | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | MSL | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | MSL | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | MSL | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | MSL | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | STU | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | STU | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | BEB | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0255 | SAS | BEB | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | BEB | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | BEB | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0265 | SAS | STU | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | STU | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | BEB | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | BEB | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | STU | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | STU | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | STU | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0267 | SAS | STU | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | YRI | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | YRI | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | CHB | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CHB | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | YRI | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | YRI | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | LWK | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | LWK | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | LWK | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | LWK | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0294 | AFR | ASW | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ASW | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0109 | EUR | TSI | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0236 | EUR | TSI | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0098 | EUR | TSI | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0211 | EUR | TSI | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | GIH | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | GIH | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | CLM | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | CLM | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | ACB | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | ACB | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | ACB | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0297 | AFR | MSL | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | MSL | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | USA | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | USA | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | USA | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | USA | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | LWK | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | LWK | TAF12_chr1_28597850_28648067 | TAF12 | chr1 | 28597850 | 28648067 |
| view | chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:28603090 | CCT | C | 1 | a0001c0001t0002 | 8 | HG01069.hp1 HG01243.hp2 HG02486.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*447_*448delAG | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 6/6 | 447 | chr1 | 28603090 | ||||||
| chr1:28603104 | A | G | 1 | a0001c0001t0004 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*435T>C | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 6/6 | 435 | chr1 | 28603104 | ||||||
| chr1:28643027 | A | C | 1 | a0001c0001t0003 | 1 | HG01255.hp1 | 5_prime_UTR_variant | MODIFIER | c.-120T>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/6 | 20946 | chr1 | 28643027 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:28603908 | C | CT | 51 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(48): Show | 51 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.451-335dupA | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 5/5 | chr1 | 28603908 | |||||||
| chr1:28604118 | T | C | 3 | a0001c0001t0001g0042a0001c0001t0001g0162a0001c0001t0001g0163 | 3 | NA18972.hp1 NA19012.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.451-544A>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 5/5 | chr1 | 28604118 | |||||||
| chr1:28604158 | G | A | 7 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0216others(4): Show | 7 | HG02055.hp1 HG02559.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.451-584C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 5/5 | chr1 | 28604158 | |||||||
| chr1:28604201 | G | A | 3 | a0001c0001t0001g0283a0001c0001t0001g0284a0001c0001t0001g0285 | 3 | HG01255.hp2 HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.451-627C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 5/5 | chr1 | 28604201 | |||||||
| chr1:28604220 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.451-646C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 5/5 | chr1 | 28604220 | |||||||
| chr1:28604249 | A | G | 1 | a0001c0001t0001g0065 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.451-675T>C | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 5/5 | chr1 | 28604249 | |||||||
| chr1:28604612 | G | C | 1 | a0001c0001t0001g0127 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.450+760C>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 5/5 | chr1 | 28604612 | |||||||
| chr1:28604894 | G | A | 1 | a0001c0001t0001g0270 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.450+478C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 5/5 | chr1 | 28604894 | |||||||
| chr1:28604948 | A | T | 1 | a0001c0001t0001g0060 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.450+424T>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 5/5 | chr1 | 28604948 | |||||||
| chr1:28605113 | T | G | 50 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(47): Show | 50 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.450+259A>C | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 5/5 | chr1 | 28605113 | |||||||
| chr1:28605259 | G | A | 3 | a0001c0001t0001g0042a0001c0001t0001g0162a0001c0001t0001g0163 | 3 | NA18972.hp1 NA19012.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.450+113C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 5/5 | chr1 | 28605259 | |||||||
| chr1:28605266 | G | T | 1 | a0001c0001t0001g0046 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.450+106C>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 5/5 | chr1 | 28605266 | |||||||
| chr1:28605500 | AAGGCAGT others(3): Show |
A | 4 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(1): Show | 4 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.362-50_362-41delGG others(8): Show |
TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28605500 | |||||||
| chr1:28605504 | C | T | 9 | a0001c0001t0001g0076a0001c0001t0001g0084a0001c0001t0001g0099others(6): Show | 9 | HG02056.hp1 HG02523.hp1 HG04184.hp1 others(6): Show |
intron_variant | MODIFIER | c.362-44G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28605504 | |||||||
| chr1:28606171 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.362-711C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28606171 | |||||||
| chr1:28606232 | C | T | 2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.362-772G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28606232 | |||||||
| chr1:28606239 | C | T | 4 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(1): Show | 4 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.362-779G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28606239 | |||||||
| chr1:28606248 | C | T | 4 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(1): Show | 4 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.362-788G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28606248 | |||||||
| chr1:28606398 | C | T | 10 | a0001c0001t0001g0026a0001c0001t0001g0152a0001c0001t0001g0179others(7): Show | 10 | HG02258.hp1 HG02809.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.362-938G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28606398 | |||||||
| chr1:28606482 | A | G | 15 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0217others(12): Show | 15 | HG00735.hp2 HG00741.hp1 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.362-1022T>C | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28606482 | |||||||
| chr1:28606821 | T | G | 3 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025 | 3 | HG01243.hp1 HG01884.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.362-1361A>C | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28606821 | |||||||
| chr1:28606824 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.362-1364G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28606824 | |||||||
| chr1:28607004 | C | T | 2 | a0001c0001t0001g0134a0001c0001t0001g0301 | 2 | NA18967.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.362-1544G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28607004 | |||||||
| chr1:28607211 | T | C | 57 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(54): Show | 57 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.362-1751A>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28607211 | |||||||
| chr1:28607349 | T | C | 1 | a0001c0001t0001g0190 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.362-1889A>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28607349 | |||||||
| chr1:28607862 | C | A | 1 | a0001c0001t0001g0080 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.362-2402G>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28607862 | |||||||
| chr1:28607879 | G | C | 1 | a0001c0001t0001g0301 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.362-2419C>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28607879 | |||||||
| chr1:28608058 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.362-2598C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28608058 | |||||||
| chr1:28608175 | C | CA | 40 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0019others(37): Show | 40 | HG00733.hp2 HG01074.hp1 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.362-2716dupT | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28608175 | |||||||
| chr1:28608175 | CA | C | 12 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(9): Show | 12 | HG01167.hp1 HG01243.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.362-2716delT | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28608175 | |||||||
| chr1:28608390 | A | G | 15 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0217others(12): Show | 15 | HG00735.hp2 HG00741.hp1 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.362-2930T>C | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28608390 | |||||||
| chr1:28608475 | C | T | 1 | a0001c0001t0004g0178 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.362-3015G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28608475 | |||||||
| chr1:28608582 | C | T | 1 | a0001c0001t0001g0293 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.362-3122G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28608582 | |||||||
| chr1:28608670 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.362-3210C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28608670 | |||||||
| chr1:28608713 | C | T | 2 | a0001c0001t0001g0209a0001c0001t0001g0227 | 2 | HG02970.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.362-3253G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28608713 | |||||||
| chr1:28608719 | C | T | 1 | a0001c0001t0001g0038 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.362-3259G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28608719 | |||||||
| chr1:28608951 | T | G | 1 | a0001c0001t0001g0031 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.362-3491A>C | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28608951 | |||||||
| chr1:28609027 | G | A | 61 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0030others(58): Show | 61 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.362-3567C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28609027 | |||||||
| chr1:28609233 | C | T | 2 | a0001c0001t0001g0192a0001c0001t0001g0272 | 2 | HG01884.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.362-3773G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28609233 | |||||||
| chr1:28609344 | G | C | 1 | a0001c0001t0001g0271 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.362-3884C>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28609344 | |||||||
| chr1:28609532 | G | C | 1 | a0001c0001t0001g0202 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.361+3715C>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28609532 | |||||||
| chr1:28609557 | G | C | 1 | a0001c0001t0001g0202 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.361+3690C>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28609557 | |||||||
| chr1:28609634 | G | A | 4 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(1): Show | 4 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.361+3613C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28609634 | |||||||
| chr1:28609717 | C | G | 8 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0060others(5): Show | 8 | HG00673.hp1 HG02132.hp1 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.361+3530G>C | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28609717 | |||||||
| chr1:28610186 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.361+3061G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28610186 | |||||||
| chr1:28610829 | G | A | 1 | a0001c0001t0004g0178 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.361+2418C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28610829 | |||||||
| chr1:28610957 | C | CA | 28 | a0001c0001t0001g0019a0001c0001t0001g0033a0001c0001t0001g0034others(25): Show | 28 | HG00140.hp2 HG01109.hp1 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.361+2289dupT | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28610957 | |||||||
| chr1:28610969 | A | C | 2 | a0001c0001t0001g0070a0001c0001t0001g0071 | 2 | HG02040.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.361+2278T>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28610969 | |||||||
| chr1:28610971 | A | C | 3 | a0001c0001t0001g0078a0001c0001t0001g0081a0001c0001t0001g0170 | 3 | HG01069.hp2 HG02486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.361+2276T>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28610971 | |||||||
| chr1:28610971 | AAAAAAAA others(6): Show |
A | 57 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(54): Show | 57 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.361+2263_361+2275d others(15): Show |
TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28610971 | |||||||
| chr1:28610972 | A | C | 7 | a0001c0001t0001g0071a0001c0001t0001g0089a0001c0001t0001g0090others(4): Show | 7 | HG00438.hp2 HG00558.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.361+2275T>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28610972 | |||||||
| chr1:28610986 | C | G | 57 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(54): Show | 57 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.361+2261G>C | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28610986 | |||||||
| chr1:28611008 | C | A | 1 | a0001c0001t0001g0172 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.361+2239G>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28611008 | |||||||
| chr1:28611108 | G | C | 2 | a0001c0001t0001g0192a0001c0001t0001g0272 | 2 | HG01884.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.361+2139C>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28611108 | |||||||
| chr1:28611126 | T | A | 1 | a0001c0001t0001g0137 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.361+2121A>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28611126 | |||||||
| chr1:28611131 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.361+2116C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28611131 | |||||||
| chr1:28611202 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.361+2045A>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28611202 | |||||||
| chr1:28611211 | G | A | 2 | a0001c0001t0001g0192a0001c0001t0001g0272 | 2 | HG01884.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.361+2036C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28611211 | |||||||
| chr1:28611339 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.361+1908C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28611339 | |||||||
| chr1:28611375 | A | T | 57 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(54): Show | 57 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.361+1872T>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28611375 | |||||||
| chr1:28611391 | A | G | 1 | a0001c0001t0001g0236 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.361+1856T>C | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28611391 | |||||||
| chr1:28611401 | G | T | 1 | a0001c0001t0001g0138 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.361+1846C>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28611401 | |||||||
| chr1:28611484 | T | C | 1 | a0001c0001t0001g0024 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.361+1763A>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28611484 | |||||||
| chr1:28611557 | GAC | G | 59 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0030others(56): Show | 59 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.361+1688_361+1689d others(4): Show |
TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28611557 | |||||||
| chr1:28611672 | T | C | 1 | a0001c0001t0001g0206 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.361+1575A>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28611672 | |||||||
| chr1:28611990 | T | C | 299 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(296): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.361+1257A>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28611990 | |||||||
| chr1:28612031 | T | C | 1 | a0001c0001t0001g0256 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.361+1216A>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28612031 | |||||||
| chr1:28612128 | G | A | 1 | a0001c0001t0004g0178 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.361+1119C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28612128 | |||||||
| chr1:28612249 | A | C | 1 | a0001c0001t0002g0014 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.361+998T>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28612249 | |||||||
| chr1:28612418 | G | A | 15 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0217others(12): Show | 15 | HG00735.hp2 HG00741.hp1 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.361+829C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28612418 | |||||||
| chr1:28612438 | C | A | 1 | a0001c0001t0001g0236 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.361+809G>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28612438 | |||||||
| chr1:28612444 | A | T | 1 | a0001c0001t0001g0028 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.361+803T>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28612444 | |||||||
| chr1:28612446 | T | A | 66 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(63): Show | 66 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.361+801A>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28612446 | |||||||
| chr1:28612448 | T | A | 2 | a0001c0001t0001g0256a0001c0001t0004g0178 | 2 | HG02145.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.361+799A>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28612448 | |||||||
| chr1:28612493 | T | C | 5 | a0001c0001t0001g0021a0001c0001t0001g0234a0001c0001t0001g0249others(2): Show | 5 | HG00738.hp2 HG01358.hp2 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.361+754A>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28612493 | |||||||
| chr1:28612507 | AAAATTAT others(14): Show |
A | 1 | a0001c0001t0002g0011 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.361+719_361+739del others(21): Show |
TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28612507 | |||||||
| chr1:28612516 | TATAA | T | 9 | a0001c0001t0001g0026a0001c0001t0001g0179a0001c0001t0001g0180others(6): Show | 9 | HG02258.hp1 HG02809.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.361+727_361+730del others(4): Show |
TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28612516 | |||||||
| chr1:28612567 | C | CAT | 35 | a0001c0001t0001g0016a0001c0001t0001g0030a0001c0001t0001g0031others(32): Show | 35 | HG00099.hp1 HG00597.hp1 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.361+678_361+679dup others(2): Show |
TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28612567 | |||||||
| chr1:28612626 | C | T | 57 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(54): Show | 57 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.361+621G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28612626 | |||||||
| chr1:28612768 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.361+479C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28612768 | |||||||
| chr1:28612849 | G | T | 1 | a0001c0001t0001g0225 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.361+398C>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 4/5 | chr1 | 28612849 | |||||||
| chr1:28613604 | A | G | 4 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(1): Show | 4 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.247-243T>C | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 3/5 | chr1 | 28613604 | |||||||
| chr1:28613986 | C | T | 300 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(297): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.247-625G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 3/5 | chr1 | 28613986 | |||||||
| chr1:28614021 | C | T | 59 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0030others(56): Show | 59 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.247-660G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 3/5 | chr1 | 28614021 | |||||||
| chr1:28614098 | C | T | 1 | a0001c0001t0001g0121 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.247-737G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 3/5 | chr1 | 28614098 | |||||||
| chr1:28614192 | C | T | 3 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185 | 3 | HG02970.hp1 HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.247-831G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 3/5 | chr1 | 28614192 | |||||||
| chr1:28614215 | C | T | 1 | a0001c0001t0001g0044 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.247-854G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 3/5 | chr1 | 28614215 | |||||||
| chr1:28614369 | G | C | 1 | a0001c0001t0001g0039 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.247-1008C>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 3/5 | chr1 | 28614369 | |||||||
| chr1:28614381 | T | C | 9 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0169others(6): Show | 9 | HG00323.hp2 HG01109.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.247-1020A>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 3/5 | chr1 | 28614381 | |||||||
| chr1:28614457 | G | T | 1 | a0001c0001t0001g0272 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.247-1096C>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 3/5 | chr1 | 28614457 | |||||||
| chr1:28614607 | G | A | 2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.247-1246C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 3/5 | chr1 | 28614607 | |||||||
| chr1:28614674 | C | CA | 16 | a0001c0001t0001g0001a0001c0001t0001g0106a0001c0001t0001g0147others(13): Show | 17 | HG02280.hp2 HG02300.hp2 HG02717.hp2 others(14): Show |
intron_variant | MODIFIER | c.247-1314dupT | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 3/5 | chr1 | 28614674 | |||||||
| chr1:28614724 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.247-1363G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 3/5 | chr1 | 28614724 | |||||||
| chr1:28614821 | G | A | 10 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0002g0005others(7): Show | 10 | HG01069.hp1 HG01243.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.247-1460C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 3/5 | chr1 | 28614821 | |||||||
| chr1:28614949 | A | G | 4 | a0001c0001t0001g0041a0001c0001t0001g0151a0001c0001t0001g0152others(1): Show | 4 | HG02809.hp1 HG02818.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.247-1588T>C | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 3/5 | chr1 | 28614949 | |||||||
| chr1:28615678 | C | CA | 16 | a0001c0001t0001g0019a0001c0001t0001g0026a0001c0001t0001g0048others(13): Show | 16 | HG00597.hp1 HG01516.hp2 HG02040.hp2 others(13): Show |
intron_variant | MODIFIER | c.246+2274dupT | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 3/5 | chr1 | 28615678 | |||||||
| chr1:28615678 | CA | C | 110 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(107): Show | 111 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.246+2274delT | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 3/5 | chr1 | 28615678 | |||||||
| chr1:28615678 | CAA | C | 45 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0013others(42): Show | 45 | HG00733.hp2 HG01074.hp1 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.246+2273_246+2274d others(4): Show |
TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 3/5 | chr1 | 28615678 | |||||||
| chr1:28615678 | CAAA | C | 28 | a0001c0001t0001g0015a0001c0001t0001g0027a0001c0001t0001g0076others(25): Show | 28 | HG00639.hp2 HG00735.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.246+2272_246+2274d others(5): Show |
TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 3/5 | chr1 | 28615678 | |||||||
| chr1:28615678 | CAAAA | C | 32 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0175others(29): Show | 32 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.246+2271_246+2274d others(6): Show |
TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 3/5 | chr1 | 28615678 | |||||||
| chr1:28615678 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0001g0180 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.246+2262_246+2274d others(15): Show |
TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 3/5 | chr1 | 28615678 | |||||||
| chr1:28615678 | CAAAAAAA others(11): Show |
C | 2 | a0001c0001t0001g0105a0001c0001t0001g0194 | 2 | HG03704.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.246+2257_246+2274d others(20): Show |
TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 3/5 | chr1 | 28615678 | |||||||
| chr1:28615678 | CAAAAAAA others(12): Show |
C | 1 | a0001c0001t0001g0051 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.246+2256_246+2274d others(21): Show |
TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 3/5 | chr1 | 28615678 | |||||||
| chr1:28615678 | CAAAAAAA others(15): Show |
C | 1 | a0001c0001t0001g0275 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.246+2253_246+2274d others(24): Show |
TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 3/5 | chr1 | 28615678 | |||||||
| chr1:28615814 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.246+2139G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 3/5 | chr1 | 28615814 | |||||||
| chr1:28616120 | G | A | 3 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025 | 3 | HG01243.hp1 HG01884.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.246+1833C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 3/5 | chr1 | 28616120 | |||||||
| chr1:28616171 | C | T | 5 | a0001c0001t0001g0001a0001c0001t0001g0214a0001c0001t0001g0215others(2): Show | 6 | HG02717.hp2 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.246+1782G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 3/5 | chr1 | 28616171 | |||||||
| chr1:28616172 | A | G | 5 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(2): Show | 5 | HG01243.hp1 HG01884.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.246+1781T>C | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 3/5 | chr1 | 28616172 | |||||||
| chr1:28616288 | C | T | 9 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0169others(6): Show | 9 | HG00323.hp2 HG01109.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.246+1665G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 3/5 | chr1 | 28616288 | |||||||
| chr1:28616375 | A | G | 5 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(2): Show | 5 | HG01243.hp1 HG01884.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.246+1578T>C | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 3/5 | chr1 | 28616375 | |||||||
| chr1:28616395 | C | CA | 11 | a0001c0001t0001g0031a0001c0001t0001g0060a0001c0001t0001g0062others(8): Show | 11 | HG00673.hp1 HG01891.hp1 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.246+1557dupT | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 3/5 | chr1 | 28616395 | |||||||
| chr1:28616395 | CA | C | 8 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0104others(5): Show | 8 | HG00323.hp2 HG01255.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.246+1557delT | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 3/5 | chr1 | 28616395 | |||||||
| chr1:28616407 | A | G | 1 | a0001c0001t0001g0225 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.246+1546T>C | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 3/5 | chr1 | 28616407 | |||||||
| chr1:28616503 | T | G | 1 | a0001c0001t0001g0026 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.246+1450A>C | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 3/5 | chr1 | 28616503 | |||||||
| chr1:28616513 | A | G | 5 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(2): Show | 5 | HG01243.hp1 HG01884.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.246+1440T>C | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 3/5 | chr1 | 28616513 | |||||||
| chr1:28616558 | C | G | 1 | a0001c0001t0001g0046 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.246+1395G>C | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 3/5 | chr1 | 28616558 | |||||||
| chr1:28616741 | T | A | 50 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(47): Show | 50 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.246+1212A>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 3/5 | chr1 | 28616741 | |||||||
| chr1:28616967 | A | C | 2 | a0001c0001t0001g0192a0001c0001t0001g0272 | 2 | HG01884.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.246+986T>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 3/5 | chr1 | 28616967 | |||||||
| chr1:28616988 | T | C | 299 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(296): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.246+965A>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 3/5 | chr1 | 28616988 | |||||||
| chr1:28617013 | A | G | 76 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(73): Show | 76 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.246+940T>C | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 3/5 | chr1 | 28617013 | |||||||
| chr1:28617116 | G | A | 4 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(1): Show | 4 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+837C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 3/5 | chr1 | 28617116 | |||||||
| chr1:28617720 | G | A | 50 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(47): Show | 50 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.246+233C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 3/5 | chr1 | 28617720 | |||||||
| chr1:28617746 | T | C | 5 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(2): Show | 5 | HG01243.hp1 HG01884.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.246+207A>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 3/5 | chr1 | 28617746 | |||||||
| chr1:28617901 | T | C | 1 | a0001c0001t0001g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.246+52A>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 3/5 | chr1 | 28617901 | |||||||
| chr1:28618069 | A | G | 1 | a0001c0001t0001g0268 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.169-39T>C | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 2/5 | chr1 | 28618069 | |||||||
| chr1:28618339 | A | G | 2 | a0001c0001t0001g0192a0001c0001t0001g0272 | 2 | HG01884.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.169-309T>C | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 2/5 | chr1 | 28618339 | |||||||
| chr1:28618434 | G | C | 1 | a0001c0001t0004g0178 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.169-404C>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 2/5 | chr1 | 28618434 | |||||||
| chr1:28618534 | A | AT | 17 | a0001c0001t0001g0015a0001c0001t0001g0042a0001c0001t0001g0043others(14): Show | 17 | HG01175.hp2 HG01261.hp1 HG02135.hp1 others(14): Show |
intron_variant | MODIFIER | c.169-505dupA | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 2/5 | chr1 | 28618534 | |||||||
| chr1:28618534 | AT | A | 23 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0025others(20): Show | 23 | HG00099.hp2 HG01099.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.169-505delA | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 2/5 | chr1 | 28618534 | |||||||
| chr1:28618833 | C | T | 1 | a0001c0001t0001g0272 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.169-803G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 2/5 | chr1 | 28618833 | |||||||
| chr1:28619089 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.169-1059G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 2/5 | chr1 | 28619089 | |||||||
| chr1:28619090 | G | A | 1 | a0001c0001t0001g0026 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.169-1060C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 2/5 | chr1 | 28619090 | |||||||
| chr1:28619260 | G | A | 50 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(47): Show | 50 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.169-1230C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 2/5 | chr1 | 28619260 | |||||||
| chr1:28619268 | C | A | 1 | a0001c0001t0001g0020 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.169-1238G>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 2/5 | chr1 | 28619268 | |||||||
| chr1:28619350 | T | G | 1 | a0001c0001t0001g0255 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.169-1320A>C | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 2/5 | chr1 | 28619350 | |||||||
| chr1:28619435 | T | C | 1 | a0001c0001t0001g0093 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.169-1405A>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 2/5 | chr1 | 28619435 | |||||||
| chr1:28619497 | C | CA | 12 | a0001c0001t0001g0033a0001c0001t0001g0041a0001c0001t0001g0042others(9): Show | 12 | HG00323.hp2 HG02055.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.169-1468dupT | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 2/5 | chr1 | 28619497 | |||||||
| chr1:28619497 | CA | C | 10 | a0001c0001t0001g0001a0001c0001t0001g0212a0001c0001t0001g0213others(7): Show | 11 | HG02055.hp1 HG02559.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.169-1468delT | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 2/5 | chr1 | 28619497 | |||||||
| chr1:28619647 | G | GA | 38 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0028others(35): Show | 38 | HG00609.hp1 HG00741.hp1 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.169-1618dupT | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 2/5 | chr1 | 28619647 | |||||||
| chr1:28619647 | GA | G | 51 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(48): Show | 51 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.169-1618delT | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 2/5 | chr1 | 28619647 | |||||||
| chr1:28619648 | A | G | 1 | a0001c0001t0001g0298 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.169-1618T>C | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 2/5 | chr1 | 28619648 | |||||||
| chr1:28620058 | G | T | 1 | a0001c0001t0001g0105 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.168+1856C>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 2/5 | chr1 | 28620058 | |||||||
| chr1:28620138 | T | A | 3 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0118 | 3 | HG01167.hp1 HG01169.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.168+1776A>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 2/5 | chr1 | 28620138 | |||||||
| chr1:28620298 | T | A | 1 | a0001c0001t0001g0066 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.168+1616A>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 2/5 | chr1 | 28620298 | |||||||
| chr1:28620442 | A | AT | 6 | a0001c0001t0001g0057a0001c0001t0001g0072a0001c0001t0001g0140others(3): Show | 6 | HG01261.hp1 HG02135.hp1 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.168+1471dupA | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 2/5 | chr1 | 28620442 | |||||||
| chr1:28620555 | C | T | 1 | a0001c0001t0004g0178 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.168+1359G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 2/5 | chr1 | 28620555 | |||||||
| chr1:28620584 | T | C | 1 | a0001c0001t0001g0066 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.168+1330A>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 2/5 | chr1 | 28620584 | |||||||
| chr1:28620626 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.168+1288G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 2/5 | chr1 | 28620626 | |||||||
| chr1:28620675 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.168+1239G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 2/5 | chr1 | 28620675 | |||||||
| chr1:28620699 | C | T | 4 | a0001c0001t0001g0174a0001c0001t0001g0254a0001c0001t0001g0257others(1): Show | 4 | HG01123.hp1 HG01167.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.168+1215G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 2/5 | chr1 | 28620699 | |||||||
| chr1:28620777 | G | T | 9 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0169others(6): Show | 9 | HG00323.hp2 HG01109.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.168+1137C>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 2/5 | chr1 | 28620777 | |||||||
| chr1:28620814 | T | TA | 57 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(54): Show | 57 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.168+1099dupT | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 2/5 | chr1 | 28620814 | |||||||
| chr1:28620953 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.168+961G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 2/5 | chr1 | 28620953 | |||||||
| chr1:28621400 | T | C | 3 | a0001c0001t0001g0130a0001c0001t0001g0132a0001c0001t0001g0156 | 3 | HG02040.hp2 NA18941.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.168+514A>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 2/5 | chr1 | 28621400 | |||||||
| chr1:28621409 | C | T | 1 | a0001c0001t0001g0162 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.168+505G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 2/5 | chr1 | 28621409 | |||||||
| chr1:28621635 | C | T | 1 | a0001c0001t0001g0106 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.168+279G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 2/5 | chr1 | 28621635 | |||||||
| chr1:28621656 | A | G | 1 | a0001c0001t0001g0088 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.168+258T>C | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 2/5 | chr1 | 28621656 | |||||||
| chr1:28622343 | G | A | 1 | a0001c0001t0004g0178 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-84-178C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28622343 | |||||||
| chr1:28622360 | G | GA | 87 | a0001c0001t0001g0016a0001c0001t0001g0022a0001c0001t0001g0028others(84): Show | 87 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.-84-196dupT | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28622360 | |||||||
| chr1:28622491 | C | T | 1 | a0001c0001t0001g0181 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-84-326G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28622491 | |||||||
| chr1:28622907 | C | T | 1 | a0001c0001t0004g0178 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-84-742G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28622907 | |||||||
| chr1:28622970 | TGA | T | 50 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(47): Show | 50 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.-84-807_-84-806del others(2): Show |
TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28622970 | |||||||
| chr1:28623036 | C | CA | 9 | a0001c0001t0001g0072a0001c0001t0001g0088a0001c0001t0001g0140others(6): Show | 9 | HG01175.hp2 HG02135.hp1 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.-84-872dupT | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28623036 | |||||||
| chr1:28623043 | A | C | 1 | a0001c0001t0001g0190 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-84-878T>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28623043 | |||||||
| chr1:28623047 | AC | A | 3 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0025 | 3 | HG01243.hp1 HG01884.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.-84-883delG | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28623047 | |||||||
| chr1:28623048 | C | A | 52 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(49): Show | 52 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.-84-883G>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28623048 | |||||||
| chr1:28623287 | C | T | 14 | a0001c0001t0001g0001a0001c0001t0001g0209a0001c0001t0001g0212others(11): Show | 15 | HG02055.hp1 HG02559.hp1 HG02717.hp2 others(12): Show |
intron_variant | MODIFIER | c.-84-1122G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28623287 | |||||||
| chr1:28623469 | C | A | 4 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(1): Show | 4 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-84-1304G>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28623469 | |||||||
| chr1:28623487 | A | AAAAT | 161 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(158): Show | 161 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.-84-1326_-84-1323d others(6): Show |
TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28623487 | |||||||
| chr1:28623487 | A | AAAATAAA others(1): Show |
13 | a0001c0001t0001g0001a0001c0001t0001g0176a0001c0001t0001g0177others(10): Show | 14 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-84-1330_-84-1323d others(10): Show |
TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28623487 | |||||||
| chr1:28623487 | A | AAAATAAA others(5): Show |
3 | a0001c0001t0001g0209a0001c0001t0001g0226a0001c0001t0001g0227 | 3 | HG02970.hp2 HG06807.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-84-1334_-84-1323d others(14): Show |
TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28623487 | |||||||
| chr1:28623588 | A | C | 1 | a0001c0001t0004g0178 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-84-1423T>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28623588 | |||||||
| chr1:28623721 | T | C | 1 | a0001c0001t0001g0133 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-84-1556A>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28623721 | |||||||
| chr1:28624350 | C | T | 57 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(54): Show | 57 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.-84-2185G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28624350 | |||||||
| chr1:28624409 | C | T | 1 | a0001c0001t0001g0296 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-84-2244G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28624409 | |||||||
| chr1:28624623 | T | C | 1 | a0001c0001t0004g0178 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-84-2458A>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28624623 | |||||||
| chr1:28624638 | T | C | 1 | a0001c0001t0001g0026 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-84-2473A>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28624638 | |||||||
| chr1:28624733 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-84-2568G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28624733 | |||||||
| chr1:28624734 | G | A | 1 | a0001c0001t0004g0178 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-84-2569C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28624734 | |||||||
| chr1:28624746 | C | CA | 53 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(50): Show | 53 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.-84-2582dupT | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28624746 | |||||||
| chr1:28624748 | A | G | 2 | a0001c0001t0001g0192a0001c0001t0001g0272 | 2 | HG01884.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-84-2583T>C | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28624748 | |||||||
| chr1:28624783 | T | G | 2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-84-2618A>C | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28624783 | |||||||
| chr1:28624786 | G | T | 50 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(47): Show | 50 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.-84-2621C>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28624786 | |||||||
| chr1:28625202 | G | A | 2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-84-3037C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28625202 | |||||||
| chr1:28625286 | C | T | 9 | a0001c0001t0001g0015a0001c0001t0001g0174a0001c0001t0001g0248others(6): Show | 9 | HG01123.hp1 HG01167.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.-84-3121G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28625286 | |||||||
| chr1:28625424 | G | A | 9 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0169others(6): Show | 9 | HG00323.hp2 HG01109.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.-84-3259C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28625424 | |||||||
| chr1:28625461 | C | T | 1 | a0001c0001t0001g0154 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-84-3296G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28625461 | |||||||
| chr1:28625537 | A | AT | 50 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0019others(47): Show | 51 | HG00741.hp1 HG01106.hp2 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.-84-3373dupA | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28625537 | |||||||
| chr1:28625537 | AT | A | 6 | a0001c0001t0001g0033a0001c0001t0001g0037a0001c0001t0001g0111others(3): Show | 6 | HG00323.hp2 HG01167.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.-84-3373delA | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28625537 | |||||||
| chr1:28625660 | G | C | 10 | a0001c0001t0001g0026a0001c0001t0001g0179a0001c0001t0001g0180others(7): Show | 10 | HG02258.hp1 HG02809.hp2 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.-84-3495C>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28625660 | |||||||
| chr1:28625669 | G | A | 2 | a0001c0001t0001g0172a0001c0001t0001g0206 | 2 | NA19075.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.-84-3504C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28625669 | |||||||
| chr1:28625713 | T | C | 1 | a0001c0001t0001g0298 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-84-3548A>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28625713 | |||||||
| chr1:28625763 | G | C | 50 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(47): Show | 50 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.-84-3598C>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28625763 | |||||||
| chr1:28625832 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-84-3667G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28625832 | |||||||
| chr1:28625848 | AT | A | 18 | a0001c0001t0001g0030a0001c0001t0001g0047a0001c0001t0001g0137others(15): Show | 18 | HG01109.hp1 HG01258.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.-84-3684delA | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28625848 | |||||||
| chr1:28625891 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-84-3726C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28625891 | |||||||
| chr1:28626170 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-84-4005C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28626170 | |||||||
| chr1:28626517 | G | C | 1 | a0001c0001t0001g0051 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-84-4352C>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28626517 | |||||||
| chr1:28626558 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-84-4393C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28626558 | |||||||
| chr1:28626581 | C | CA | 23 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0077others(20): Show | 23 | HG00438.hp1 HG00735.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.-84-4417dupT | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28626581 | |||||||
| chr1:28626612 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-84-4447A>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28626612 | |||||||
| chr1:28626630 | C | T | 1 | a0001c0001t0004g0178 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-84-4465G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28626630 | |||||||
| chr1:28626706 | C | T | 15 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0217others(12): Show | 15 | HG00735.hp2 HG00741.hp1 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.-84-4541G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28626706 | |||||||
| chr1:28626712 | C | T | 3 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185 | 3 | HG02970.hp1 HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-84-4547G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28626712 | |||||||
| chr1:28626786 | T | C | 1 | a0001c0001t0001g0028 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-84-4621A>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28626786 | |||||||
| chr1:28626818 | G | A | 14 | a0001c0001t0001g0001a0001c0001t0001g0209a0001c0001t0001g0212others(11): Show | 15 | HG02055.hp1 HG02559.hp1 HG02717.hp2 others(12): Show |
intron_variant | MODIFIER | c.-84-4653C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28626818 | |||||||
| chr1:28626868 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-84-4703G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28626868 | |||||||
| chr1:28626990 | A | T | 1 | a0001c0001t0001g0282 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-84-4825T>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28626990 | |||||||
| chr1:28627125 | G | A | 1 | a0001c0001t0004g0178 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-84-4960C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28627125 | |||||||
| chr1:28627285 | G | C | 1 | a0001c0001t0001g0190 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-84-5120C>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28627285 | |||||||
| chr1:28627380 | T | C | 1 | a0001c0001t0001g0210 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-84-5215A>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28627380 | |||||||
| chr1:28627391 | G | GA | 22 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0026others(19): Show | 23 | HG01243.hp1 HG01928.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.-84-5227dupT | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28627391 | |||||||
| chr1:28627391 | GA | G | 11 | a0001c0001t0001g0098a0001c0001t0001g0175a0001c0001t0001g0238others(8): Show | 11 | HG01517.hp1 HG01928.hp2 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.-84-5227delT | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28627391 | |||||||
| chr1:28627419 | C | T | 1 | a0001c0001t0001g0026 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-84-5254G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28627419 | |||||||
| chr1:28627420 | G | A | 1 | a0001c0001t0001g0028 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-84-5255C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28627420 | |||||||
| chr1:28627426 | G | A | 3 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0118 | 3 | HG01167.hp1 HG01169.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.-84-5261C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28627426 | |||||||
| chr1:28627464 | C | T | 49 | a0001c0001t0001g0018a0001c0001t0001g0028a0001c0001t0001g0033others(46): Show | 49 | HG00099.hp2 HG00438.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.-84-5299G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28627464 | |||||||
| chr1:28627480 | T | G | 3 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0166 | 3 | HG01074.hp1 HG01099.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.-84-5315A>C | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28627480 | |||||||
| chr1:28627485 | A | C | 1 | a0001c0001t0001g0060 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-84-5320T>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28627485 | |||||||
| chr1:28627562 | G | A | 1 | a0001c0001t0001g0281 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-84-5397C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28627562 | |||||||
| chr1:28627619 | G | T | 1 | a0001c0001t0001g0255 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-84-5454C>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28627619 | |||||||
| chr1:28627644 | G | T | 1 | a0001c0001t0001g0043 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-84-5479C>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28627644 | |||||||
| chr1:28627648 | G | A | 1 | a0001c0001t0001g0182 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-84-5483C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28627648 | |||||||
| chr1:28627665 | C | CA | 183 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0013others(180): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.-84-5501dupT | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28627665 | |||||||
| chr1:28627665 | C | CAA | 55 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0028others(52): Show | 55 | HG00323.hp2 HG00609.hp1 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.-84-5502_-84-5501d others(4): Show |
TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28627665 | |||||||
| chr1:28627665 | CAAAAAA | C | 47 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(44): Show | 47 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.-84-5506_-84-5501d others(8): Show |
TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28627665 | |||||||
| chr1:28627734 | T | C | 1 | a0001c0001t0001g0018 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-84-5569A>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28627734 | |||||||
| chr1:28627768 | G | C | 1 | a0001c0001t0001g0225 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-84-5603C>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28627768 | |||||||
| chr1:28627858 | A | C | 1 | a0001c0001t0004g0178 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-84-5693T>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28627858 | |||||||
| chr1:28628216 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-84-6051G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28628216 | |||||||
| chr1:28628222 | A | G | 4 | a0001c0001t0001g0151a0001c0001t0001g0216a0001c0001t0002g0005others(1): Show | 4 | HG01243.hp2 HG02818.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.-84-6057T>C | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28628222 | |||||||
| chr1:28628228 | T | G | 20 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0041others(17): Show | 20 | HG00438.hp1 HG01069.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.-84-6063A>C | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28628228 | |||||||
| chr1:28628228 | T | TG | 25 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0018others(22): Show | 25 | HG01257.hp2 HG01258.hp1 HG01261.hp2 others(22): Show |
intron_variant | MODIFIER | c.-84-6064dupC | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28628228 | |||||||
| chr1:28628228 | T | TGG | 57 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0022others(54): Show | 58 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(55): Show |
intron_variant | MODIFIER | c.-84-6065_-84-6064d others(4): Show |
TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28628228 | |||||||
| chr1:28628228 | T | TGGG | 50 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0029others(47): Show | 50 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.-84-6066_-84-6064d others(5): Show |
TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28628228 | |||||||
| chr1:28628228 | T | TGGGG | 43 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0036others(40): Show | 43 | HG00609.hp2 HG00673.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.-84-6067_-84-6064d others(6): Show |
TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28628228 | |||||||
| chr1:28628228 | T | TGGGGG | 33 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0031others(30): Show | 33 | HG00597.hp1 HG00597.hp2 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.-84-6068_-84-6064d others(7): Show |
TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28628228 | |||||||
| chr1:28628228 | T | TGGGGGG | 30 | a0001c0001t0001g0024a0001c0001t0001g0032a0001c0001t0001g0048others(27): Show | 30 | HG00099.hp1 HG00639.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.-84-6069_-84-6064d others(8): Show |
TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28628228 | |||||||
| chr1:28628228 | T | TGGGGGGG others(3): Show |
4 | a0001c0001t0001g0025a0001c0001t0001g0030a0001c0001t0001g0047others(1): Show | 4 | HG01243.hp1 HG01258.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-84-6073_-84-6064d others(12): Show |
TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28628228 | |||||||
| chr1:28628228 | T | TGGGGGGG others(4): Show |
2 | a0001c0001t0001g0049a0001c0001t0001g0179 | 2 | HG02809.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.-84-6074_-84-6064d others(13): Show |
TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28628228 | |||||||
| chr1:28628243 | C | G | 7 | a0001c0001t0001g0017a0001c0001t0001g0102a0001c0001t0001g0142others(4): Show | 7 | HG01358.hp1 HG01515.hp2 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.-84-6078G>C | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28628243 | |||||||
| chr1:28628278 | TG | T | 50 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(47): Show | 50 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.-84-6114delC | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28628278 | |||||||
| chr1:28628308 | T | G | 1 | a0001c0001t0001g0073 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-84-6143A>C | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28628308 | |||||||
| chr1:28628338 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-84-6173G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28628338 | |||||||
| chr1:28628411 | G | T | 8 | a0001c0001t0001g0026a0001c0001t0001g0179a0001c0001t0001g0180others(5): Show | 8 | HG02809.hp2 HG02970.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.-84-6246C>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28628411 | |||||||
| chr1:28628564 | T | C | 2 | a0001c0001t0001g0270a0001c0001t0001g0271 | 2 | HG02258.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-84-6399A>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28628564 | |||||||
| chr1:28628609 | A | C | 1 | a0001c0001t0004g0178 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-84-6444T>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28628609 | |||||||
| chr1:28628643 | G | C | 2 | a0001c0001t0001g0192a0001c0001t0001g0272 | 2 | HG01884.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-84-6478C>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28628643 | |||||||
| chr1:28628675 | TA | T | 17 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0022others(14): Show | 17 | HG00323.hp2 HG01074.hp1 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.-84-6511delT | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28628675 | |||||||
| chr1:28628778 | G | A | 5 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(2): Show | 5 | HG01243.hp1 HG01884.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.-84-6613C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28628778 | |||||||
| chr1:28628823 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-84-6658C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28628823 | |||||||
| chr1:28628894 | G | T | 3 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0292 | 3 | HG01109.hp1 HG02717.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-84-6729C>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28628894 | |||||||
| chr1:28629014 | T | C | 2 | a0001c0001t0001g0043a0001c0001t0001g0051 | 2 | HG02738.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.-84-6849A>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28629014 | |||||||
| chr1:28629128 | T | G | 1 | a0001c0001t0001g0140 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-84-6963A>C | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28629128 | |||||||
| chr1:28629595 | C | T | 2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-84-7430G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28629595 | |||||||
| chr1:28629667 | A | G | 1 | a0001c0001t0001g0048 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-84-7502T>C | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28629667 | |||||||
| chr1:28629681 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-84-7516G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28629681 | |||||||
| chr1:28629822 | A | T | 10 | a0001c0001t0001g0026a0001c0001t0001g0179a0001c0001t0001g0180others(7): Show | 10 | HG02258.hp1 HG02809.hp2 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.-84-7657T>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28629822 | |||||||
| chr1:28630043 | T | A | 1 | a0001c0001t0001g0143 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-84-7878A>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28630043 | |||||||
| chr1:28630426 | C | T | 3 | a0001c0001t0001g0036a0001c0001t0001g0096a0001c0001t0001g0101 | 3 | HG00140.hp2 HG00735.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.-84-8261G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28630426 | |||||||
| chr1:28630447 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-84-8282C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28630447 | |||||||
| chr1:28630484 | G | A | 18 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0074others(15): Show | 18 | HG00438.hp2 HG00558.hp1 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.-84-8319C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28630484 | |||||||
| chr1:28630509 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-84-8344C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28630509 | |||||||
| chr1:28630559 | A | G | 51 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(48): Show | 51 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.-84-8394T>C | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28630559 | |||||||
| chr1:28630640 | G | A | 4 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(1): Show | 4 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-84-8475C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28630640 | |||||||
| chr1:28630684 | CAAAAG | C | 8 | a0001c0001t0001g0027a0001c0001t0001g0186a0001c0001t0001g0187others(5): Show | 8 | HG00639.hp2 HG02280.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-84-8524_-84-8520d others(7): Show |
TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28630684 | |||||||
| chr1:28630692 | A | T | 1 | a0001c0001t0001g0100 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-84-8527T>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28630692 | |||||||
| chr1:28630693 | A | T | 1 | a0001c0001t0001g0100 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-84-8528T>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28630693 | |||||||
| chr1:28630760 | G | A | 15 | a0001c0001t0001g0001a0001c0001t0001g0209a0001c0001t0001g0212others(12): Show | 16 | HG02055.hp1 HG02145.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.-84-8595C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28630760 | |||||||
| chr1:28630815 | G | A | 1 | a0001c0001t0001g0095 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-84-8650C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28630815 | |||||||
| chr1:28631026 | T | G | 4 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(1): Show | 4 | HG00099.hp1 HG01106.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.-84-8861A>C | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28631026 | |||||||
| chr1:28631045 | C | CA | 20 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0033others(17): Show | 20 | HG00323.hp2 HG01109.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.-84-8881dupT | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28631045 | |||||||
| chr1:28631045 | CA | C | 6 | a0001c0001t0001g0044a0001c0001t0001g0099a0001c0001t0001g0151others(3): Show | 6 | HG01192.hp2 HG02523.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-84-8881delT | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28631045 | |||||||
| chr1:28631071 | T | C | 1 | a0001c0001t0004g0178 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-84-8906A>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28631071 | |||||||
| chr1:28631099 | A | G | 1 | a0001c0001t0001g0291 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-84-8934T>C | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28631099 | |||||||
| chr1:28631209 | TAAC | T | 4 | a0001c0001t0001g0232a0001c0001t0001g0242a0001c0001t0001g0250others(1): Show | 4 | HG00609.hp2 HG01099.hp2 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.-84-9047_-84-9045d others(5): Show |
TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28631209 | |||||||
| chr1:28631231 | G | A | 2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-84-9066C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28631231 | |||||||
| chr1:28631305 | T | C | 2 | a0001c0001t0001g0017a0001c0001t0001g0142 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-84-9140A>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28631305 | |||||||
| chr1:28631442 | C | T | 5 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(2): Show | 5 | HG01243.hp1 HG01884.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.-84-9277G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28631442 | |||||||
| chr1:28631535 | A | G | 2 | a0001c0001t0001g0049a0001c0001t0001g0055 | 2 | HG02735.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.-84-9370T>C | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28631535 | |||||||
| chr1:28632103 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-84-9938A>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28632103 | |||||||
| chr1:28632260 | A | T | 1 | a0001c0001t0001g0050 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-84-10095T>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28632260 | |||||||
| chr1:28632264 | G | GCT | 5 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(2): Show | 5 | HG01243.hp1 HG01884.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.-84-10101_-84-1010 others(6): Show |
TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28632264 | |||||||
| chr1:28632440 | C | T | 7 | a0001c0001t0001g0043a0001c0001t0001g0050a0001c0001t0001g0051others(4): Show | 7 | HG00099.hp1 HG01106.hp2 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.-84-10275G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28632440 | |||||||
| chr1:28632464 | A | G | 9 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0169others(6): Show | 9 | HG00323.hp2 HG01109.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.-84-10299T>C | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28632464 | |||||||
| chr1:28632548 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-84-10383G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28632548 | |||||||
| chr1:28632950 | G | A | 2 | a0001c0001t0001g0192a0001c0001t0001g0272 | 2 | HG01884.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-85+10042C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28632950 | |||||||
| chr1:28633015 | C | G | 1 | a0001c0001t0001g0098 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-85+9977G>C | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28633015 | |||||||
| chr1:28633022 | C | A | 1 | a0001c0001t0001g0143 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-85+9970G>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28633022 | |||||||
| chr1:28633133 | T | A | 1 | a0001c0001t0001g0217 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-85+9859A>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28633133 | |||||||
| chr1:28633164 | C | CT | 14 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0041others(11): Show | 14 | HG00735.hp1 HG01175.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.-85+9827dupA | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28633164 | |||||||
| chr1:28633283 | C | A | 4 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(1): Show | 4 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-85+9709G>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28633283 | |||||||
| chr1:28633411 | A | C | 4 | a0001c0001t0001g0173a0001c0001t0001g0175a0001c0001t0001g0259others(1): Show | 4 | HG02080.hp1 NA18957.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.-85+9581T>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28633411 | |||||||
| chr1:28633467 | C | T | 1 | a0001c0001t0004g0178 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-85+9525G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28633467 | |||||||
| chr1:28633624 | A | G | 1 | a0001c0001t0001g0197 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-85+9368T>C | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28633624 | |||||||
| chr1:28633740 | C | T | 1 | a0001c0001t0004g0178 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-85+9252G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28633740 | |||||||
| chr1:28633912 | CA | C | 49 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0017others(46): Show | 49 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.-85+9079delT | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28633912 | |||||||
| chr1:28633954 | G | T | 7 | a0001c0001t0001g0209a0001c0001t0001g0212a0001c0001t0001g0213others(4): Show | 7 | HG02055.hp1 HG02559.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-85+9038C>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28633954 | |||||||
| chr1:28633975 | C | T | 1 | a0001c0001t0001g0252 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-85+9017G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28633975 | |||||||
| chr1:28634006 | C | T | 10 | a0001c0001t0001g0026a0001c0001t0001g0179a0001c0001t0001g0180others(7): Show | 10 | HG02258.hp1 HG02809.hp2 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.-85+8986G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28634006 | |||||||
| chr1:28634211 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-85+8781G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28634211 | |||||||
| chr1:28634215 | A | C | 7 | a0001c0001t0001g0209a0001c0001t0001g0212a0001c0001t0001g0213others(4): Show | 7 | HG02055.hp1 HG02559.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-85+8777T>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28634215 | |||||||
| chr1:28634226 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-85+8766G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28634226 | |||||||
| chr1:28634285 | G | A | 2 | a0001c0001t0001g0030a0001c0001t0001g0047 | 2 | HG01258.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.-85+8707C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28634285 | |||||||
| chr1:28634393 | G | A | 1 | a0001c0001t0001g0275 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-85+8599C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28634393 | |||||||
| chr1:28634415 | C | CA | 32 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0027others(29): Show | 32 | HG00609.hp1 HG00639.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.-85+8576dupT | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28634415 | |||||||
| chr1:28634430 | A | C | 1 | a0001c0001t0001g0083 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-85+8562T>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28634430 | |||||||
| chr1:28634436 | A | C | 2 | a0001c0001t0001g0174a0001c0001t0002g0011 | 2 | HG01167.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.-85+8556T>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28634436 | |||||||
| chr1:28634437 | C | A | 2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-85+8555G>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28634437 | |||||||
| chr1:28634472 | T | C | 3 | a0001c0001t0001g0283a0001c0001t0001g0284a0001c0001t0001g0285 | 3 | HG01255.hp2 HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-85+8520A>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28634472 | |||||||
| chr1:28634550 | G | C | 1 | a0001c0001t0004g0178 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-85+8442C>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28634550 | |||||||
| chr1:28634571 | T | C | 5 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(2): Show | 5 | HG01243.hp1 HG01884.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.-85+8421A>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28634571 | |||||||
| chr1:28635124 | G | A | 1 | a0001c0001t0004g0178 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-85+7868C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28635124 | |||||||
| chr1:28635154 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-85+7838G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28635154 | |||||||
| chr1:28635184 | C | T | 2 | a0001c0001t0001g0192a0001c0001t0001g0272 | 2 | HG01884.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-85+7808G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28635184 | |||||||
| chr1:28635249 | T | A | 1 | a0001c0001t0001g0297 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-85+7743A>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28635249 | |||||||
| chr1:28635253 | A | T | 4 | a0001c0001t0001g0083a0001c0001t0001g0176a0001c0001t0001g0177others(1): Show | 4 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.-85+7739T>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28635253 | |||||||
| chr1:28635257 | A | C | 14 | a0001c0001t0001g0001a0001c0001t0001g0209a0001c0001t0001g0212others(11): Show | 15 | HG02055.hp1 HG02559.hp1 HG02717.hp2 others(12): Show |
intron_variant | MODIFIER | c.-85+7735T>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28635257 | |||||||
| chr1:28635276 | C | CT | 43 | a0001c0001t0001g0017a0001c0001t0001g0026a0001c0001t0001g0030others(40): Show | 43 | HG00438.hp2 HG00597.hp2 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.-85+7715dupA | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28635276 | |||||||
| chr1:28635276 | CT | C | 40 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(37): Show | 40 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.-85+7715delA | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28635276 | |||||||
| chr1:28635276 | CTTTTTTT others(4): Show |
C | 4 | a0001c0001t0001g0041a0001c0001t0001g0151a0001c0001t0001g0152others(1): Show | 4 | HG02809.hp1 HG02818.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-85+7705_-85+7715d others(13): Show |
TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28635276 | |||||||
| chr1:28635278 | T | C | 3 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150 | 3 | NA18995.hp2 NA19011.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.-85+7714A>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28635278 | |||||||
| chr1:28635279 | T | C | 2 | a0001c0001t0001g0149a0001c0001t0001g0150 | 2 | NA18995.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.-85+7713A>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28635279 | |||||||
| chr1:28635317 | TGTGTCGC others(15): Show |
T | 2 | a0001c0001t0001g0030a0001c0001t0001g0047 | 2 | HG01258.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.-85+7653_-85+7674d others(24): Show |
TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28635317 | |||||||
| chr1:28635345 | G | A | 1 | a0001c0001t0001g0154 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-85+7647C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28635345 | |||||||
| chr1:28635589 | G | A | 1 | a0001c0001t0004g0178 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-85+7403C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28635589 | |||||||
| chr1:28635814 | GT | G | 7 | a0001c0001t0001g0072a0001c0001t0001g0155a0001c0001t0001g0156others(4): Show | 7 | HG01167.hp2 HG01255.hp1 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.-85+7177delA | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28635814 | |||||||
| chr1:28635826 | T | A | 3 | a0001c0001t0001g0046a0001c0001t0001g0250a0001c0001t0004g0178 | 3 | HG00609.hp2 HG02145.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.-85+7166A>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28635826 | |||||||
| chr1:28635826 | T | TA | 7 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0001g0158others(4): Show | 7 | HG01358.hp1 HG01943.hp2 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.-85+7165_-85+7166i others(3): Show |
TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28635826 | |||||||
| chr1:28635827 | T | A | 288 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(285): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.-85+7165A>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28635827 | |||||||
| chr1:28635827 | T | TA | 5 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0001g0245others(2): Show | 5 | HG00323.hp1 HG00741.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.-85+7164dupT | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28635827 | |||||||
| chr1:28635981 | G | A | 1 | a0001c0001t0001g0267 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-85+7011C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28635981 | |||||||
| chr1:28636121 | G | A | 10 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0169others(7): Show | 10 | HG00323.hp2 HG00597.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-85+6871C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28636121 | |||||||
| chr1:28636136 | G | C | 1 | a0001c0001t0001g0244 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-85+6856C>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28636136 | |||||||
| chr1:28636207 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-85+6785C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28636207 | |||||||
| chr1:28636351 | T | G | 1 | a0001c0001t0001g0271 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-85+6641A>C | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28636351 | |||||||
| chr1:28636533 | A | G | 5 | a0001c0001t0001g0217a0001c0001t0001g0219a0001c0001t0001g0220others(2): Show | 5 | HG00735.hp2 HG00741.hp1 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.-85+6459T>C | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28636533 | |||||||
| chr1:28636707 | G | A | 3 | a0001c0001t0001g0042a0001c0001t0001g0162a0001c0001t0001g0163 | 3 | NA18972.hp1 NA19012.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.-85+6285C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28636707 | |||||||
| chr1:28636847 | T | G | 4 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(1): Show | 4 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-85+6145A>C | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28636847 | |||||||
| chr1:28636864 | T | C | 1 | a0001c0001t0001g0285 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-85+6128A>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28636864 | |||||||
| chr1:28636891 | T | G | 2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-85+6101A>C | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28636891 | |||||||
| chr1:28636998 | GTTTCA | G | 76 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(73): Show | 76 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.-85+5989_-85+5993d others(7): Show |
TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28636998 | |||||||
| chr1:28637088 | C | T | 1 | a0001c0001t0001g0251 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-85+5904G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28637088 | |||||||
| chr1:28637117 | T | TAAC | 5 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(2): Show | 5 | HG01243.hp1 HG01884.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.-85+5872_-85+5874d others(5): Show |
TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28637117 | |||||||
| chr1:28637289 | G | A | 2 | a0001c0001t0001g0209a0001c0001t0001g0216 | 2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-85+5703C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28637289 | |||||||
| chr1:28637316 | T | C | 1 | a0001c0001t0001g0245 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-85+5676A>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28637316 | |||||||
| chr1:28637392 | T | C | 57 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(54): Show | 57 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.-85+5600A>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28637392 | |||||||
| chr1:28637408 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-85+5584A>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28637408 | |||||||
| chr1:28637432 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-85+5560G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28637432 | |||||||
| chr1:28637448 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-85+5544G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28637448 | |||||||
| chr1:28637521 | C | T | 35 | a0001c0001t0001g0016a0001c0001t0001g0030a0001c0001t0001g0031others(32): Show | 35 | HG00099.hp1 HG00597.hp1 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.-85+5471G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28637521 | |||||||
| chr1:28637534 | G | A | 50 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(47): Show | 50 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.-85+5458C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28637534 | |||||||
| chr1:28637775 | T | C | 50 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(47): Show | 50 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.-85+5217A>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28637775 | |||||||
| chr1:28637869 | C | A | 1 | a0001c0001t0001g0165 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-85+5123G>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28637869 | |||||||
| chr1:28637869 | C | T | 2 | a0001c0001t0001g0030a0001c0001t0001g0047 | 2 | HG01258.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.-85+5123G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28637869 | |||||||
| chr1:28637870 | G | A | 1 | a0001c0001t0001g0246 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-85+5122C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28637870 | |||||||
| chr1:28637886 | C | T | 12 | a0001c0001t0001g0001a0001c0001t0001g0209a0001c0001t0001g0212others(9): Show | 13 | HG02055.hp1 HG02559.hp1 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.-85+5106G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28637886 | |||||||
| chr1:28638010 | A | T | 1 | a0001c0001t0001g0186 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-85+4982T>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28638010 | |||||||
| chr1:28638173 | G | GTATTT | 3 | a0001c0001t0001g0234a0001c0001t0001g0249a0001c0001t0001g0250 | 3 | HG00609.hp2 HG00738.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.-85+4814_-85+4818d others(7): Show |
TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28638173 | |||||||
| chr1:28638173 | G | GTATTTTA others(8): Show |
2 | a0001c0001t0001g0270a0001c0001t0001g0271 | 2 | HG02258.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-85+4804_-85+4818d others(17): Show |
TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28638173 | |||||||
| chr1:28638173 | GTATTTTA others(3): Show |
G | 1 | a0001c0001t0001g0266 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-85+4809_-85+4818d others(12): Show |
TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28638173 | |||||||
| chr1:28638346 | C | T | 4 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(1): Show | 4 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-85+4646G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28638346 | |||||||
| chr1:28638385 | C | T | 4 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(1): Show | 4 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-85+4607G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28638385 | |||||||
| chr1:28638437 | C | T | 3 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025 | 3 | HG01243.hp1 HG01884.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-85+4555G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28638437 | |||||||
| chr1:28638479 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-85+4513C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28638479 | |||||||
| chr1:28638480 | C | A | 1 | a0001c0001t0001g0271 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-85+4512G>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28638480 | |||||||
| chr1:28638491 | A | AT | 13 | a0001c0001t0001g0024a0001c0001t0001g0043a0001c0001t0001g0044others(10): Show | 13 | HG00733.hp2 HG00735.hp2 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.-85+4500dupA | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28638491 | |||||||
| chr1:28638787 | A | AT | 46 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0024others(43): Show | 47 | HG00140.hp1 HG00609.hp1 HG01099.hp2 others(44): Show |
intron_variant | MODIFIER | c.-85+4204dupA | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28638787 | |||||||
| chr1:28638885 | G | A | 5 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(2): Show | 5 | HG01106.hp1 HG01243.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.-85+4107C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28638885 | |||||||
| chr1:28638948 | G | C | 1 | a0001c0001t0001g0166 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-85+4044C>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28638948 | |||||||
| chr1:28639027 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-85+3965C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28639027 | |||||||
| chr1:28639043 | G | C | 1 | a0001c0001t0001g0285 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-85+3949C>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28639043 | |||||||
| chr1:28639101 | A | C | 1 | a0001c0001t0004g0178 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-85+3891T>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28639101 | |||||||
| chr1:28639182 | C | T | 1 | a0001c0001t0001g0029 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-85+3810G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28639182 | |||||||
| chr1:28639317 | G | A | 1 | a0001c0001t0001g0168 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-85+3675C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28639317 | |||||||
| chr1:28639426 | C | CAAAAAAA others(7): Show |
4 | a0001c0001t0001g0022a0001c0001t0001g0169a0001c0001t0001g0207others(1): Show | 4 | HG00323.hp2 HG01123.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-85+3552_-85+3565d others(16): Show |
TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28639426 | |||||||
| chr1:28639426 | C | CAAAAAAA others(8): Show |
42 | a0001c0001t0001g0023a0001c0001t0001g0026a0001c0001t0001g0027others(39): Show | 42 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.-85+3551_-85+3565d others(17): Show |
TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28639426 | |||||||
| chr1:28639426 | C | CAAAAAAA others(9): Show |
56 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(53): Show | 57 | HG00609.hp2 HG00741.hp1 HG00741.hp2 others(54): Show |
intron_variant | MODIFIER | c.-85+3565_-85+3566i others(18): Show |
TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28639426 | |||||||
| chr1:28639426 | C | CAAAAAAA others(10): Show |
12 | a0001c0001t0001g0013a0001c0001t0001g0192a0001c0001t0001g0221others(9): Show | 12 | HG00735.hp2 HG01074.hp2 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.-85+3565_-85+3566i others(19): Show |
TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28639426 | |||||||
| chr1:28639426 | C | CAAAAAAA others(11): Show |
2 | a0001c0001t0001g0272a0001c0001t0002g0014 | 2 | HG02486.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-85+3565_-85+3566i others(20): Show |
TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28639426 | |||||||
| chr1:28639506 | G | A | 2 | a0001c0001t0001g0171a0001c0001t0001g0172 | 2 | NA18953.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.-85+3486C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28639506 | |||||||
| chr1:28639698 | T | C | 4 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(1): Show | 4 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-85+3294A>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28639698 | |||||||
| chr1:28639750 | T | C | 1 | a0001c0001t0004g0178 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-85+3242A>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28639750 | |||||||
| chr1:28639883 | C | T | 1 | a0001c0001t0001g0028 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-85+3109G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28639883 | |||||||
| chr1:28640032 | G | A | 2 | a0001c0001t0001g0175a0001c0001t0001g0269 | 2 | NA18957.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.-85+2960C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28640032 | |||||||
| chr1:28640102 | C | T | 10 | a0001c0001t0001g0026a0001c0001t0001g0179a0001c0001t0001g0180others(7): Show | 10 | HG02258.hp1 HG02809.hp2 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.-85+2890G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28640102 | |||||||
| chr1:28641014 | A | G | 57 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(54): Show | 57 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.-85+1978T>C | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28641014 | |||||||
| chr1:28641244 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-85+1748C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28641244 | |||||||
| chr1:28641257 | G | A | 2 | a0001c0001t0001g0226a0001c0001t0001g0227 | 2 | HG02970.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-85+1735C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28641257 | |||||||
| chr1:28641269 | A | G | 76 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(73): Show | 76 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.-85+1723T>C | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28641269 | |||||||
| chr1:28641340 | G | A | 2 | a0001c0001t0001g0230a0001c0001t0001g0231 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-85+1652C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28641340 | |||||||
| chr1:28641508 | T | C | 1 | a0001c0001t0001g0228 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-85+1484A>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28641508 | |||||||
| chr1:28641655 | G | A | 1 | a0001c0001t0001g0229 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-85+1337C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28641655 | |||||||
| chr1:28641775 | C | G | 50 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(47): Show | 50 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.-85+1217G>C | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28641775 | |||||||
| chr1:28641786 | C | A | 2 | a0001c0001t0001g0230a0001c0001t0001g0231 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-85+1206G>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28641786 | |||||||
| chr1:28641793 | C | CA | 78 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(75): Show | 79 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.-85+1198dupT | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28641793 | |||||||
| chr1:28641793 | C | CAA | 49 | a0001c0001t0001g0015a0001c0001t0001g0232a0001c0001t0001g0233others(46): Show | 49 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.-85+1197_-85+1198d others(4): Show |
TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28641793 | |||||||
| chr1:28641793 | CA | C | 6 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(3): Show | 6 | HG01515.hp2 HG02109.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-85+1198delT | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28641793 | |||||||
| chr1:28641816 | T | A | 6 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277others(3): Show | 6 | HG01928.hp2 HG01943.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.-85+1176A>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28641816 | |||||||
| chr1:28641818 | C | T | 1 | a0001c0001t0001g0015 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-85+1174G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28641818 | |||||||
| chr1:28641902 | G | A | 1 | a0001c0001t0001g0281 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-85+1090C>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28641902 | |||||||
| chr1:28642307 | T | A | 1 | a0001c0001t0001g0282 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-85+685A>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28642307 | |||||||
| chr1:28642489 | T | C | 3 | a0001c0001t0001g0283a0001c0001t0001g0284a0001c0001t0001g0285 | 3 | HG01255.hp2 HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-85+503A>G | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28642489 | |||||||
| chr1:28642589 | A | T | 10 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0002g0005others(7): Show | 10 | HG01069.hp1 HG01243.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-85+403T>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28642589 | |||||||
| chr1:28642775 | C | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-85+217G>A | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28642775 | |||||||
| chr1:28642802 | A | G | 286 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(283): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.-85+190T>C | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28642802 | |||||||
| chr1:28642856 | C | A | 1 | a0001c0001t0001g0301 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-85+136G>T | TAF12 | ENSG00000120656.14 | transcript | ENST00000373824.9 | protein_coding | 1/5 | chr1 | 28642856 |