Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 7024 |
| ensemblid | ENSG00000135457.11 |
| hgncid | 11748 |
| symbol | TFCP2 |
| name | transcription factor CP2 |
| refseq_nuc | NM_005653.5 |
| refseq_prot | NP_005644.2 |
| ensembl_nuc | ENST00000257915.10 |
| ensembl_prot | ENSP00000257915.5 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 51093656 |
| end | 51173135 |
| strand | - |
| ver | v1.2 |
| region | chr12:51093656-51173135 |
| region5000 | chr12:51088656-51178135 |
| regionname0 | TFCP2_chr12_51093656_51173135 |
| regionname5000 | TFCP2_chr12_51088656_51178135 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1506 | 347 | 92 | 72 | 131 | 12 | 38 | TFCP2_chr12_51088656_51178135 | TFCP2 | ATGGC others(1501): Show |
chr12 | 51088656 | 51178135 | ||
| a0001c0002 | 0/0 | 1506 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | ATGGC others(1501): Show |
chr12 | 51088656 | 51178135 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3793 | 92 | 25 | 10 | 46 | 2 | 9 | TFCP2_chr12_51088656_51178135 | TFCP2 | GTTCG others(3788): Show |
chr12 | 51088656 | 51178135 |
| a0001c0001t0002 | 0/0 | 3805 | 68 | 19 | 27 | 10 | 5 | 7 | TFCP2_chr12_51088656_51178135 | TFCP2 | GTTCG others(3800): Show |
chr12 | 51088656 | 51178135 |
| a0001c0001t0003 | 0/0 | 3805 | 48 | 4 | 11 | 24 | 2 | 7 | TFCP2_chr12_51088656_51178135 | TFCP2 | GTTCG others(3800): Show |
chr12 | 51088656 | 51178135 |
| a0001c0001t0004 | 0/0 | 3811 | 44 | 4 | 11 | 28 | 0 | 1 | TFCP2_chr12_51088656_51178135 | TFCP2 | GTTCG others(3806): Show |
chr12 | 51088656 | 51178135 |
| a0001c0001t0005 | 0/0 | 3807 | 16 | 10 | 1 | 0 | 0 | 5 | TFCP2_chr12_51088656_51178135 | TFCP2 | GTTCG others(3802): Show |
chr12 | 51088656 | 51178135 |
| a0001c0001t0006 | 0/0 | 3807 | 12 | 12 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | GTTCG others(3802): Show |
chr12 | 51088656 | 51178135 |
| a0001c0001t0007 | 1/0 | 3807 | 6 | 5 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | GTTCG others(3802): Show |
chr12 | 51088656 | 51178135 |
| a0001c0001t0008 | 0/0 | 3805 | 5 | 1 | 1 | 3 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | GTTCG others(3800): Show |
chr12 | 51088656 | 51178135 |
| a0001c0001t0009 | 0/0 | 3813 | 5 | 0 | 0 | 5 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | GTTCG others(3808): Show |
chr12 | 51088656 | 51178135 |
| a0001c0001t0010 | 0/0 | 3807 | 5 | 1 | 2 | 1 | 0 | 1 | TFCP2_chr12_51088656_51178135 | TFCP2 | GTTCG others(3802): Show |
chr12 | 51088656 | 51178135 |
| a0001c0001t0011 | 0/0 | 3805 | 4 | 0 | 0 | 3 | 1 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | GTTCG others(3800): Show |
chr12 | 51088656 | 51178135 |
| a0001c0001t0012 | 0/0 | 3805 | 4 | 1 | 3 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | GTTCG others(3800): Show |
chr12 | 51088656 | 51178135 |
| a0001c0001t0013 | 0/0 | 3805 | 4 | 4 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | GTTCG others(3800): Show |
chr12 | 51088656 | 51178135 |
| a0001c0001t0014 | 0/0 | 3805 | 3 | 0 | 0 | 3 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | GTTCG others(3800): Show |
chr12 | 51088656 | 51178135 |
| a0001c0001t0015 | 0/0 | 3811 | 3 | 0 | 0 | 3 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | GTTCG others(3806): Show |
chr12 | 51088656 | 51178135 |
| a0001c0001t0016 | 0/0 | 3805 | 3 | 1 | 0 | 1 | 0 | 1 | TFCP2_chr12_51088656_51178135 | TFCP2 | GTTCG others(3800): Show |
chr12 | 51088656 | 51178135 |
| a0001c0001t0017 | 0/0 | 3805 | 3 | 1 | 0 | 0 | 1 | 1 | TFCP2_chr12_51088656_51178135 | TFCP2 | GTTCG others(3800): Show |
chr12 | 51088656 | 51178135 |
| a0001c0001t0018 | 0/0 | 3805 | 3 | 1 | 2 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | GTTCG others(3800): Show |
chr12 | 51088656 | 51178135 |
| a0001c0001t0019 | 0/0 | 3807 | 2 | 0 | 0 | 0 | 1 | 1 | TFCP2_chr12_51088656_51178135 | TFCP2 | GTTCG others(3802): Show |
chr12 | 51088656 | 51178135 |
| a0001c0001t0020 | 0/0 | 3805 | 2 | 0 | 0 | 0 | 0 | 2 | TFCP2_chr12_51088656_51178135 | TFCP2 | GTTCG others(3800): Show |
chr12 | 51088656 | 51178135 |
| a0001c0001t0021 | 0/0 | 3805 | 2 | 0 | 0 | 0 | 0 | 2 | TFCP2_chr12_51088656_51178135 | TFCP2 | GTTCG others(3800): Show |
chr12 | 51088656 | 51178135 |
| a0001c0001t0022 | 0/0 | 3811 | 2 | 0 | 2 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | GTTCG others(3806): Show |
chr12 | 51088656 | 51178135 |
| a0001c0001t0023 | 0/0 | 3793 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | GTTCG others(3788): Show |
chr12 | 51088656 | 51178135 |
| a0001c0001t0024 | 0/0 | 3775 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | GTTCG others(3770): Show |
chr12 | 51088656 | 51178135 |
| a0001c0001t0025 | 0/0 | 3807 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | GTTCG others(3802): Show |
chr12 | 51088656 | 51178135 |
| a0001c0001t0026 | 0/0 | 3793 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | GTTCG others(3788): Show |
chr12 | 51088656 | 51178135 |
| a0001c0001t0027 | 0/0 | 3807 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | GTTCG others(3802): Show |
chr12 | 51088656 | 51178135 |
| a0001c0001t0028 | 0/0 | 3811 | 1 | 0 | 0 | 0 | 0 | 1 | TFCP2_chr12_51088656_51178135 | TFCP2 | GTTCG others(3806): Show |
chr12 | 51088656 | 51178135 |
| a0001c0001t0029 | 0/0 | 3793 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | GTTCG others(3788): Show |
chr12 | 51088656 | 51178135 |
| a0001c0001t0030 | 0/1 | 3807 | 1 | 0 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | GTTCG others(3802): Show |
chr12 | 51088656 | 51178135 |
| a0001c0001t0031 | 0/0 | 3807 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | GTTCG others(3802): Show |
chr12 | 51088656 | 51178135 |
| a0001c0001t0032 | 0/0 | 3775 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | GTTCG others(3770): Show |
chr12 | 51088656 | 51178135 |
| a0001c0001t0033 | 0/0 | 3793 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | GTTCG others(3788): Show |
chr12 | 51088656 | 51178135 |
| a0001c0002t0004 | 0/0 | 3811 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | GTTCG others(3806): Show |
chr12 | 51088656 | 51178135 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0001 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0007 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0002g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0003g0002 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0003g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0003g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0003g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0003g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0004g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0004g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0004g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0004g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0004g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0004g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0004g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0004g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0004g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0004g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0004g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0004g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0004g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0004g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0004g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0004g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0004g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0004g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0004g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0004g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0004g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0004g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0004g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0004g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0004g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0004g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0004g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0004g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0005g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0005g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0005g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0005g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0005g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0005g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0005g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0005g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0005g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0005g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0005g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0005g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0005g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0005g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0005g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0005g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0006g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0006g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0006g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0006g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0006g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0006g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0006g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0006g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0006g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0006g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0006g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0006g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0007g0268 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0007g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0007g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0007g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0007g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0007g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0008g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0008g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0008g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0008g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0008g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0009g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0009g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0009g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0009g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0009g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0010g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0010g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0010g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0010g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0010g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0011g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0011g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0011g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0011g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0012g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0012g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0012g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0012g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0013g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0013g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0013g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0014g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0014g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0014g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0015g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0015g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0015g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0016g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0016g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0016g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0017g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0017g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0017g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0018g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0018g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0019g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0019g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0020g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0020g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0021g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0021g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0022g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0022g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0023g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0024g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0025g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0026g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0027g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0028g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0029g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0030g0253 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0031g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0032g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0001t0033g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| a0001c0002t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0172 | EUR | GBR | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0225 | EUR | GBR | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG00140 | hp1 | a0001 | c0001 | t0017 | g0199 | EUR | GBR | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0007 | EUR | GBR | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0223 | EUR | FIN | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG00280 | hp2 | a0001 | c0001 | t0011 | g0041 | EUR | FIN | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0065 | EAS | CHS | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG00408 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | CHS | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | CHS | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG00423 | hp2 | a0001 | c0001 | t0009 | g0093 | EAS | CHS | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | CHS | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG00438 | hp2 | a0001 | c0001 | t0004 | g0080 | EAS | CHS | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | CHS | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG00544 | hp2 | a0001 | c0001 | t0015 | g0107 | EAS | CHS | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG00558 | hp1 | a0001 | c0001 | t0004 | g0091 | EAS | CHS | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | CHS | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | CHS | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG00597 | hp2 | a0001 | c0001 | t0004 | g0081 | EAS | CHS | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0050 | EAS | CHS | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG00609 | hp2 | a0001 | c0001 | t0025 | g0086 | EAS | CHS | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG00639 | hp2 | a0001 | c0001 | t0010 | g0168 | AMR | PUR | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG00642 | hp1 | a0001 | c0001 | t0026 | g0186 | AMR | PUR | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG00642 | hp2 | a0001 | c0001 | t0004 | g0113 | AMR | PUR | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0036 | AMR | PUR | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0179 | AMR | PUR | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0180 | AMR | PUR | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0098 | AMR | PUR | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0285 | AMR | PUR | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0166 | AMR | PUR | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0183 | AMR | PUR | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0040 | AMR | PUR | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG01069 | hp1 | a0001 | c0001 | t0018 | g0009 | AMR | PUR | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG01069 | hp2 | a0001 | c0001 | t0008 | g0124 | AMR | PUR | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG01070 | hp1 | a0001 | c0001 | t0022 | g0336 | AMR | PUR | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG01070 | hp2 | a0001 | c0001 | t0012 | g0158 | AMR | PUR | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG01071 | hp1 | a0001 | c0001 | t0012 | g0160 | AMR | PUR | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG01071 | hp2 | a0001 | c0001 | t0018 | g0009 | AMR | PUR | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0163 | AMR | PUR | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0138 | AMR | PUR | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | PUR | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG01099 | hp1 | a0001 | c0001 | t0012 | g0161 | AMR | PUR | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG01099 | hp2 | a0001 | c0001 | t0022 | g0337 | AMR | PUR | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0038 | AMR | PUR | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0156 | AMR | PUR | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0290 | AMR | PUR | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0068 | AMR | PUR | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0301 | AMR | PUR | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG01175 | hp1 | a0001 | c0001 | t0033 | g0338 | AMR | PUR | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0175 | AMR | PUR | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0174 | AMR | PUR | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0054 | AMR | PUR | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0181 | AMR | CLM | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0051 | AMR | CLM | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | CLM | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0162 | AMR | CLM | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0011 | AMR | CLM | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG01346 | hp2 | a0001 | c0001 | t0005 | g0122 | AMR | CLM | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0165 | AMR | CLM | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0048 | AMR | CLM | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | CLM | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG01361 | hp2 | a0001 | c0001 | t0004 | g0097 | AMR | CLM | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0282 | AMR | CLM | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0157 | AMR | CLM | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0177 | EUR | IBS | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0028 | EUR | IBS | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0167 | EUR | IBS | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0052 | EUR | IBS | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG01884 | hp1 | a0001 | c0001 | t0016 | g0302 | AFR | ACB | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0319 | AFR | ACB | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0169 | AFR | ACB | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG01928 | hp1 | a0001 | c0001 | t0004 | g0085 | AMR | PEL | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0283 | AMR | PEL | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG01934 | hp1 | a0001 | c0001 | t0010 | g0193 | AMR | PEL | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG01934 | hp2 | a0001 | c0001 | t0004 | g0074 | AMR | PEL | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG01943 | hp1 | a0001 | c0001 | t0004 | g0077 | AMR | PEL | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0281 | AMR | PEL | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0286 | AMR | PEL | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG01952 | hp2 | a0001 | c0001 | t0004 | g0103 | AMR | PEL | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0182 | AMR | PEL | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG01993 | hp1 | a0001 | c0001 | t0004 | g0095 | AMR | PEL | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PEL | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0284 | AMR | PEL | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02004 | hp2 | a0001 | c0001 | t0004 | g0092 | AMR | PEL | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0061 | EAS | KHV | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02027 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | KHV | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | KHV | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0064 | EAS | KHV | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02055 | hp2 | a0001 | c0001 | t0007 | g0269 | AFR | ACB | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | KHV | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | KHV | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02083 | hp1 | a0001 | c0001 | t0009 | g0076 | EAS | KHV | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | KHV | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | KHV | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02129 | hp2 | a0001 | c0001 | t0004 | g0079 | EAS | KHV | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02145 | hp1 | a0001 | c0001 | t0005 | g0134 | AFR | ACB | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02145 | hp2 | a0001 | c0001 | t0006 | g0314 | AFR | ACB | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0287 | AMR | PEL | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02148 | hp2 | a0001 | c0001 | t0004 | g0099 | AMR | PEL | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | CDX | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0023 | EAS | CDX | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0305 | AFR | ACB | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0072 | AFR | ACB | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02273 | hp1 | a0001 | c0001 | t0004 | g0082 | AMR | PEL | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0324 | AMR | PEL | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02280 | hp1 | a0001 | c0001 | t0007 | g0333 | AFR | ACB | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0222 | AMR | PEL | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | PEL | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0037 | AMR | PEL | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PEL | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0127 | AFR | ACB | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02523 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | KHV | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | KHV | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0197 | AFR | GWD | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0033 | AFR | GWD | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0237 | SAS | PJL | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02615 | hp1 | a0001 | c0001 | t0012 | g0159 | AFR | GWD | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | GWD | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02622 | hp1 | a0001 | c0001 | t0007 | g0270 | AFR | GWD | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0307 | AFR | GWD | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | GWD | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02630 | hp2 | a0001 | c0001 | t0032 | g0334 | AFR | GWD | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | GWD | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0032 | AFR | GWD | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0059 | SAS | PJL | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0170 | SAS | PJL | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02698 | hp1 | a0001 | c0001 | t0019 | g0034 | SAS | PJL | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02698 | hp2 | a0001 | c0001 | t0017 | g0203 | SAS | PJL | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02717 | hp1 | a0001 | c0001 | t0008 | g0132 | AFR | GWD | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0293 | AFR | GWD | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02723 | hp1 | a0001 | c0001 | t0013 | g0155 | AFR | GWD | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0320 | AFR | GWD | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0035 | SAS | PJL | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0176 | SAS | PJL | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02818 | hp1 | a0001 | c0001 | t0007 | g0332 | AFR | GWD | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0188 | AFR | GWD | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0189 | AFR | GWD | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02896 | hp1 | a0001 | c0001 | t0007 | g0331 | AFR | GWD | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02896 | hp2 | a0001 | c0001 | t0013 | g0006 | AFR | GWD | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02897 | hp1 | a0001 | c0001 | t0013 | g0006 | AFR | GWD | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0135 | AFR | GWD | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0003 | AFR | ESN | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0173 | AFR | ESN | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02965 | hp1 | a0001 | c0001 | t0029 | g0279 | AFR | ESN | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02965 | hp2 | a0001 | c0001 | t0006 | g0323 | AFR | ESN | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | ESN | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02970 | hp2 | a0001 | c0001 | t0005 | g0130 | AFR | ESN | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02976 | hp1 | a0001 | c0001 | t0006 | g0202 | AFR | ESN | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02976 | hp2 | a0001 | c0001 | t0005 | g0128 | AFR | ESN | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG03041 | hp1 | a0001 | c0001 | t0024 | g0066 | AFR | GWD | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | GWD | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0329 | AFR | ESN | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG03130 | hp2 | a0001 | c0001 | t0006 | g0200 | AFR | ESN | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0327 | AFR | ESN | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG03139 | hp2 | a0001 | c0001 | t0006 | g0328 | AFR | ESN | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG03195 | hp2 | a0001 | c0001 | t0006 | g0310 | AFR | ESN | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0304 | AFR | MSL | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | MSL | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG03225 | hp1 | a0001 | c0001 | t0006 | g0201 | AFR | MSL | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0049 | AFR | MSL | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG03239 | hp1 | a0001 | c0001 | t0005 | g0123 | SAS | PJL | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | MSL | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG03453 | hp2 | a0001 | c0001 | t0006 | g0316 | AFR | MSL | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | MSL | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0322 | AFR | MSL | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0184 | SAS | PJL | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0058 | SAS | PJL | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0057 | SAS | PJL | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0185 | SAS | PJL | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | ESN | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | ESN | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0119 | AFR | GWD | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | GWD | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0192 | AFR | MSL | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG03579 | hp2 | a0001 | c0001 | t0005 | g0131 | AFR | MSL | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG03654 | hp2 | a0001 | c0001 | t0020 | g0046 | SAS | PJL | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG03669 | hp2 | a0001 | c0001 | t0005 | g0133 | SAS | PJL | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG03688 | hp1 | a0001 | c0001 | t0020 | g0029 | SAS | STU | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG03688 | hp2 | a0001 | c0001 | t0004 | g0102 | SAS | STU | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | BEB | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG03831 | hp2 | a0001 | c0001 | t0010 | g0198 | SAS | BEB | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | BEB | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG03834 | hp2 | a0001 | c0001 | t0005 | g0118 | SAS | BEB | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0055 | SAS | BEB | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG03927 | hp2 | a0001 | c0001 | t0028 | g0330 | SAS | BEB | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0039 | SAS | BEB | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0267 | SAS | BEB | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | STU | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG04199 | hp2 | a0001 | c0001 | t0021 | g0252 | SAS | STU | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG04204 | hp1 | a0001 | c0001 | t0021 | g0289 | SAS | STU | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0056 | SAS | STU | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG04228 | hp1 | a0001 | c0001 | t0005 | g0126 | SAS | STU | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG04228 | hp2 | a0001 | c0001 | t0016 | g0204 | SAS | STU | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0298 | AFR | YRI | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18522 | hp2 | a0001 | c0001 | t0006 | g0313 | AFR | YRI | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | CHB | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18612 | hp2 | a0001 | c0001 | t0009 | g0096 | EAS | CHB | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18747 | hp1 | a0001 | c0001 | t0016 | g0206 | EAS | CHB | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18747 | hp2 | a0001 | c0001 | t0004 | g0075 | EAS | CHB | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0178 | AFR | YRI | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0121 | AFR | YRI | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18939 | hp2 | a0001 | c0001 | t0004 | g0088 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18946 | hp2 | a0001 | c0001 | t0004 | g0110 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18947 | hp1 | a0001 | c0001 | t0004 | g0108 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18949 | hp1 | a0001 | c0001 | t0010 | g0242 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18951 | hp2 | a0001 | c0001 | t0004 | g0083 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18954 | hp2 | a0001 | c0001 | t0004 | g0090 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18959 | hp2 | a0001 | c0001 | t0027 | g0244 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18961 | hp2 | a0001 | c0001 | t0004 | g0105 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18971 | hp1 | a0001 | c0001 | t0015 | g0136 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18972 | hp2 | a0001 | c0001 | t0004 | g0111 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18973 | hp1 | a0001 | c0001 | t0011 | g0047 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18973 | hp2 | a0001 | c0001 | t0004 | g0078 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18979 | hp1 | a0001 | c0001 | t0009 | g0101 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18980 | hp1 | a0001 | c0001 | t0015 | g0137 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18981 | hp1 | a0001 | c0001 | t0004 | g0100 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18981 | hp2 | a0001 | c0001 | t0011 | g0043 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18984 | hp1 | a0001 | c0001 | t0031 | g0146 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18986 | hp2 | a0001 | c0001 | t0004 | g0114 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18990 | hp1 | a0001 | c0001 | t0009 | g0094 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18991 | hp1 | a0001 | c0001 | t0004 | g0112 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18995 | hp2 | a0001 | c0001 | t0004 | g0070 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA19001 | hp1 | a0001 | c0001 | t0014 | g0019 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA19001 | hp2 | a0001 | c0001 | t0004 | g0106 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA19002 | hp2 | a0001 | c0001 | t0004 | g0089 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA19003 | hp1 | a0001 | c0001 | t0008 | g0115 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA19005 | hp1 | a0001 | c0001 | t0004 | g0087 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA19009 | hp2 | a0001 | c0001 | t0014 | g0020 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA19010 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA19011 | hp1 | a0001 | c0001 | t0008 | g0117 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA19011 | hp2 | a0001 | c0001 | t0004 | g0069 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA19012 | hp1 | a0001 | c0001 | t0008 | g0116 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0295 | AFR | LWK | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA19030 | hp2 | a0001 | c0001 | t0006 | g0312 | AFR | LWK | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0003 | AFR | LWK | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | LWK | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA19058 | hp1 | a0001 | c0001 | t0011 | g0022 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA19062 | hp2 | a0001 | c0001 | t0004 | g0109 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA19063 | hp2 | a0001 | c0001 | t0004 | g0084 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA19065 | hp2 | a0001 | c0002 | t0004 | g0071 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA19068 | hp2 | a0001 | c0001 | t0014 | g0018 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA19072 | hp1 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA19086 | hp2 | a0001 | c0001 | t0004 | g0104 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA19088 | hp1 | a0001 | c0001 | t0023 | g0012 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA19240 | hp1 | a0001 | c0001 | t0013 | g0297 | AFR | YRI | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0120 | AFR | YRI | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA20129 | hp1 | a0001 | c0001 | t0006 | g0309 | AFR | ASW | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0321 | AFR | ASW | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0150 | EUR | TSI | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA20752 | hp2 | a0001 | c0001 | t0019 | g0053 | EUR | TSI | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0191 | SAS | GIH | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA20905 | hp2 | a0001 | c0001 | t0005 | g0125 | SAS | GIH | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0299 | AFR | ACB | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0311 | AFR | ACB | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0187 | AFR | ACB | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0073 | AFR | ACB | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02559 | hp1 | a0001 | c0001 | t0018 | g0335 | AFR | ACB | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG02559 | hp2 | a0001 | c0001 | t0006 | g0315 | AFR | ACB | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0306 | AFR | MSL | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0300 | AFR | MSL | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG06807 | hp1 | a0001 | c0001 | t0010 | g0291 | AFR | USA | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| HG06807 | hp2 | a0001 | c0001 | t0017 | g0303 | AFR | USA | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0042 | AFR | USA | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0171 | AFR | USA | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0254 | AFR | LWK | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| NA21309 | hp2 | a0001 | c0001 | t0005 | g0129 | AFR | LWK | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0030 | g0253 | REF | REF | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0007 | g0268 | REF | REF | TFCP2_chr12_51088656_51178135 | TFCP2 | chr12 | 51088656 | 51178135 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:51118739 | T | C | 1 | a0001c0002 | 1 | NA19065.hp2 | synonymous_variant | LOW | c.156A>G | p.Glu52Glu | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 2/15 | 869/3807 | 156/1509 | 52/502 | chr12 | 51118739 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:51093663 | G | A | 1 | a0001c0001t0029 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1578C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 15/15 | 1578 | chr12 | 51093663 | ||||||
| chr12:51093833 | A | AACAC | 5 | a0001c0001t0004 a0001c0001t0015 a0001c0001t0022 others(2): Show |
51 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*1404_*1407dupGTGT | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 15/15 | 1407 | chr12 | 51093833 | ||||||
| chr12:51093833 | A | AACACAC | 1 | a0001c0001t0009 | 5 | HG00423.hp2 HG02083.hp1 NA18612.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1402_*1407dupGTGT others(2): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 15/15 | 1407 | chr12 | 51093833 | ||||||
| chr12:51093833 | AAC | A | 12 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0008 others(9): Show |
149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
3_prime_UTR_variant | MODIFIER | c.*1406_*1407delGT | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 15/15 | 1406 | chr12 | 51093833 | ||||||
| chr12:51093833 | AACACACA others(7): Show |
A | 7 | a0001c0001t0001 a0001c0001t0023 a0001c0001t0024 others(4): Show |
98 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*1394_*1407delGTGT others(10): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 15/15 | 1394 | chr12 | 51093833 | ||||||
| chr12:51093835 | C | CAT | 3 | a0001c0001t0005 a0001c0001t0019 a0001c0001t0027 |
19 | HG01346.hp2 HG02145.hp1 HG02451.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1405_*1406insAT | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 15/15 | 1405 | chr12 | 51093835 | ||||||
| chr12:51093933 | G | A | 1 | a0001c0001t0013 | 4 | HG02723.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1308C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 15/15 | 1308 | chr12 | 51093933 | ||||||
| chr12:51093968 | A | T | 3 | a0001c0001t0005 a0001c0001t0019 a0001c0001t0027 |
19 | HG01346.hp2 HG02145.hp1 HG02451.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1273T>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 15/15 | 1273 | chr12 | 51093968 | ||||||
| chr12:51093978 | TACACACT others(11): Show |
T | 2 | a0001c0001t0024 a0001c0001t0032 |
2 | HG02630.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1245_*1262delGTGT others(14): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 15/15 | 1245 | chr12 | 51093978 | ||||||
| chr12:51093984 | CTT | C | 5 | a0001c0001t0001 a0001c0001t0023 a0001c0001t0026 others(2): Show |
71 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*1255_*1256delAA | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 15/15 | 1255 | chr12 | 51093984 | ||||||
| chr12:51093985 | T | A | 1 | a0001c0001t0001 | 2 | HG03491.hp1 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1256A>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 15/15 | 1256 | chr12 | 51093985 | ||||||
| chr12:51093986 | T | C | 1 | a0001c0001t0001 | 2 | HG03491.hp1 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1255A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 15/15 | 1255 | chr12 | 51093986 | ||||||
| chr12:51093986 | T | TAC | 10 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(7): Show |
32 | HG00408.hp1 HG01346.hp2 HG02145.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*1253_*1254dupGT | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 15/15 | 1254 | chr12 | 51093986 | ||||||
| chr12:51093986 | T | TACACAC | 1 | a0001c0001t0002 | 3 | HG02109.hp1 HG03471.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1249_*1254dupGTGT others(2): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 15/15 | 1254 | chr12 | 51093986 | ||||||
| chr12:51093986 | TAC | T | 4 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0016 others(1): Show |
17 | HG00140.hp1 HG01884.hp1 HG01884.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1253_*1254delGT | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 15/15 | 1253 | chr12 | 51093986 | ||||||
| chr12:51093986 | TACAC | T | 1 | a0001c0001t0006 | 9 | HG02145.hp2 HG02559.hp2 HG02965.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1251_*1254delGTGT | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 15/15 | 1251 | chr12 | 51093986 | ||||||
| chr12:51093986 | TACACAC | T | 11 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0008 others(8): Show |
87 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*1249_*1254delGTGT others(2): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 15/15 | 1249 | chr12 | 51093986 | ||||||
| chr12:51094086 | C | A | 32 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(29): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
3_prime_UTR_variant | MODIFIER | c.*1155G>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 15/15 | 1155 | chr12 | 51094086 | ||||||
| chr12:51094099 | T | C | 17 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(14): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(201): Show |
3_prime_UTR_variant | MODIFIER | c.*1142A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 15/15 | 1142 | chr12 | 51094099 | ||||||
| chr12:51094314 | T | C | 1 | a0001c0001t0015 | 3 | HG00544.hp2 NA18971.hp1 NA18980.hp1 |
3_prime_UTR_variant | MODIFIER | c.*927A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 15/15 | 927 | chr12 | 51094314 | ||||||
| chr12:51094354 | C | T | 1 | a0001c0001t0021 | 2 | HG04199.hp2 HG04204.hp1 |
3_prime_UTR_variant | MODIFIER | c.*887G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 15/15 | 887 | chr12 | 51094354 | ||||||
| chr12:51094449 | G | T | 1 | a0001c0001t0026 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*792C>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 15/15 | 792 | chr12 | 51094449 | ||||||
| chr12:51094453 | A | G | 24 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(21): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(267): Show |
3_prime_UTR_variant | MODIFIER | c.*788T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 15/15 | 788 | chr12 | 51094453 | ||||||
| chr12:51094484 | G | A | 1 | a0001c0001t0013 | 4 | HG02723.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*757C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 15/15 | 757 | chr12 | 51094484 | ||||||
| chr12:51094596 | T | C | 1 | a0001c0001t0018 | 3 | HG01069.hp1 HG01071.hp2 HG02559.hp1 |
3_prime_UTR_variant | MODIFIER | c.*645A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 15/15 | 645 | chr12 | 51094596 | ||||||
| chr12:51094600 | G | A | 2 | a0001c0001t0024 a0001c0001t0032 |
2 | HG02630.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*641C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 15/15 | 641 | chr12 | 51094600 | ||||||
| chr12:51094639 | A | C | 3 | a0001c0001t0003 a0001c0001t0011 a0001c0001t0018 |
55 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*602T>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 15/15 | 602 | chr12 | 51094639 | ||||||
| chr12:51094687 | T | C | 1 | a0001c0001t0011 | 4 | HG00280.hp2 NA18973.hp1 NA18981.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*554A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 15/15 | 554 | chr12 | 51094687 | ||||||
| chr12:51095091 | G | A | 1 | a0001c0001t0031 | 1 | NA18984.hp1 | 3_prime_UTR_variant | MODIFIER | c.*150C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 15/15 | 150 | chr12 | 51095091 | ||||||
| chr12:51095226 | C | T | 1 | a0001c0001t0012 | 4 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*15G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 15/15 | 15 | chr12 | 51095226 | ||||||
| chr12:51172567 | C | T | 8 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0008 others(5): Show |
77 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(74): Show |
5_prime_UTR_variant | MODIFIER | c.-145G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/15 | 145 | chr12 | 51172567 | ||||||
| chr12:51172758 | G | A | 7 | a0001c0001t0003 a0001c0001t0011 a0001c0001t0014 others(4): Show |
61 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(58): Show |
5_prime_UTR_variant | MODIFIER | c.-336C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/15 | 336 | chr12 | 51172758 | ||||||
| chr12:51172790 | G | A | 2 | a0001c0001t0018 a0001c0001t0032 |
4 | HG01069.hp1 HG01071.hp2 HG02559.hp1 others(1): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-368C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/15 | chr12 | 51172790 | |||||||
| chr12:51172854 | C | A | 1 | a0001c0001t0022 | 2 | HG01070.hp1 HG01099.hp2 |
5_prime_UTR_variant | MODIFIER | c.-432G>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/15 | 432 | chr12 | 51172854 | ||||||
| chr12:51172874 | G | T | 7 | a0001c0001t0003 a0001c0001t0011 a0001c0001t0014 others(4): Show |
61 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(58): Show |
5_prime_UTR_variant | MODIFIER | c.-452C>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/15 | 452 | chr12 | 51172874 | ||||||
| chr12:51172884 | T | C | 1 | a0001c0001t0033 | 1 | HG01175.hp1 | 5_prime_UTR_variant | MODIFIER | c.-462A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/15 | 462 | chr12 | 51172884 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:51095557 | G | A | 4 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 others(1): Show |
4 | HG02717.hp2 HG03041.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1472-279C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 14/14 | chr12 | 51095557 | |||||||
| chr12:51095624 | G | C | 1 | a0001c0001t0013g0006 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1472-346C>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 14/14 | chr12 | 51095624 | |||||||
| chr12:51095636 | G | A | 2 | a0001c0001t0002g0304 a0001c0001t0002g0307 |
2 | HG02622.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1471+353C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 14/14 | chr12 | 51095636 | |||||||
| chr12:51095664 | A | G | 1 | a0001c0001t0005g0133 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1471+325T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 14/14 | chr12 | 51095664 | |||||||
| chr12:51095746 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1471+243C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 14/14 | chr12 | 51095746 | |||||||
| chr12:51095763 | G | A | 19 | a0001c0001t0005g0118 a0001c0001t0005g0119 a0001c0001t0005g0120 others(16): Show |
19 | HG01346.hp2 HG02145.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.1471+226C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 14/14 | chr12 | 51095763 | |||||||
| chr12:51095777 | G | A | 1 | a0001c0001t0018g0009 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1471+212C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 14/14 | chr12 | 51095777 | |||||||
| chr12:51095813 | C | CA | 132 | a0001c0001t0001g0292 a0001c0001t0001g0317 a0001c0001t0001g0318 others(129): Show |
137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.1471+175dupT | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 14/14 | chr12 | 51095813 | |||||||
| chr12:51095813 | C | CAA | 19 | a0001c0001t0002g0165 a0001c0001t0002g0171 a0001c0001t0002g0174 others(16): Show |
19 | HG01175.hp1 HG01192.hp1 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.1471+174_1471+175d others(4): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 14/14 | chr12 | 51095813 | |||||||
| chr12:51095813 | CA | C | 17 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(14): Show |
17 | HG02273.hp1 HG02451.hp2 HG02886.hp2 others(14): Show |
intron_variant | MODIFIER | c.1471+175delT | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 14/14 | chr12 | 51095813 | |||||||
| chr12:51095855 | C | T | 5 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0167 others(2): Show |
8 | HG00099.hp1 HG00140.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.1471+134G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 14/14 | chr12 | 51095855 | |||||||
| chr12:51096489 | T | G | 2 | a0001c0001t0017g0199 a0001c0001t0017g0203 |
2 | HG00140.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1420-449A>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 13/14 | chr12 | 51096489 | |||||||
| chr12:51096551 | C | T | 71 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(68): Show |
73 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.1420-511G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 13/14 | chr12 | 51096551 | |||||||
| chr12:51096581 | G | A | 79 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0138 others(76): Show |
82 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.1420-541C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 13/14 | chr12 | 51096581 | |||||||
| chr12:51096625 | G | A | 65 | a0001c0001t0003g0002 a0001c0001t0003g0010 a0001c0001t0003g0011 others(62): Show |
67 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.1420-585C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 13/14 | chr12 | 51096625 | |||||||
| chr12:51096715 | T | C | 3 | a0001c0001t0001g0238 a0001c0001t0001g0249 a0001c0001t0001g0250 |
3 | NA18612.hp1 NA18989.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.1420-675A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 13/14 | chr12 | 51096715 | |||||||
| chr12:51096899 | A | G | 328 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(325): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(335): Show |
intron_variant | MODIFIER | c.1420-859T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 13/14 | chr12 | 51096899 | |||||||
| chr12:51096949 | A | G | 2 | a0001c0001t0001g0238 a0001c0001t0001g0249 |
2 | NA18612.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.1420-909T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 13/14 | chr12 | 51096949 | |||||||
| chr12:51096952 | A | AT | 179 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(176): Show |
185 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.1420-913dupA | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 13/14 | chr12 | 51096952 | |||||||
| chr12:51097016 | C | T | 179 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(176): Show |
185 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.1420-976G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 13/14 | chr12 | 51097016 | |||||||
| chr12:51097048 | C | T | 1 | a0001c0001t0005g0133 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1420-1008G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 13/14 | chr12 | 51097048 | |||||||
| chr12:51097123 | C | A | 3 | a0001c0001t0002g0298 a0001c0001t0002g0299 a0001c0001t0002g0300 |
3 | HG02109.hp1 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1420-1083G>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 13/14 | chr12 | 51097123 | |||||||
| chr12:51097309 | C | T | 11 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0121 others(8): Show |
11 | HG01346.hp2 HG02145.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1420-1269G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 13/14 | chr12 | 51097309 | |||||||
| chr12:51097331 | C | A | 12 | a0001c0001t0006g0200 a0001c0001t0006g0201 a0001c0001t0006g0202 others(9): Show |
12 | HG02145.hp2 HG02559.hp2 HG02965.hp2 others(9): Show |
intron_variant | MODIFIER | c.1420-1291G>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 13/14 | chr12 | 51097331 | |||||||
| chr12:51097409 | A | G | 79 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0138 others(76): Show |
82 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.1419+1367T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 13/14 | chr12 | 51097409 | |||||||
| chr12:51097562 | A | G | 1 | a0001c0001t0002g0329 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1419+1214T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 13/14 | chr12 | 51097562 | |||||||
| chr12:51097698 | A | G | 3 | a0001c0001t0002g0175 a0001c0001t0002g0184 a0001c0001t0002g0185 |
3 | HG01175.hp2 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1419+1078T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 13/14 | chr12 | 51097698 | |||||||
| chr12:51097743 | G | A | 2 | a0001c0001t0001g0218 a0001c0001t0001g0246 |
2 | HG00558.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1419+1033C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 13/14 | chr12 | 51097743 | |||||||
| chr12:51097775 | G | A | 1 | a0001c0001t0003g0027 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1419+1001C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 13/14 | chr12 | 51097775 | |||||||
| chr12:51097778 | A | G | 35 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0150 others(32): Show |
38 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.1419+998T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 13/14 | chr12 | 51097778 | |||||||
| chr12:51097978 | G | A | 179 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(176): Show |
185 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.1419+798C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 13/14 | chr12 | 51097978 | |||||||
| chr12:51098383 | T | G | 1 | a0001c0001t0001g0255 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1419+393A>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 13/14 | chr12 | 51098383 | |||||||
| chr12:51098453 | C | T | 4 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0001g0233 others(1): Show |
4 | HG01978.hp1 HG01993.hp2 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.1419+323G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 13/14 | chr12 | 51098453 | |||||||
| chr12:51098476 | AT | A | 179 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(176): Show |
185 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.1419+299delA | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 13/14 | chr12 | 51098476 | |||||||
| chr12:51098518 | C | T | 179 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(176): Show |
185 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.1419+258G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 13/14 | chr12 | 51098518 | |||||||
| chr12:51098726 | G | A | 73 | a0001c0001t0004g0003 a0001c0001t0004g0004 a0001c0001t0004g0005 others(70): Show |
76 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.1419+50C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 13/14 | chr12 | 51098726 | |||||||
| chr12:51098978 | T | A | 1 | a0001c0001t0003g0040 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1277-60A>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 12/14 | chr12 | 51098978 | |||||||
| chr12:51099047 | CAACCACT others(12): Show |
C | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG02886.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1277-148_1277-130d others(21): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 12/14 | chr12 | 51099047 | |||||||
| chr12:51099477 | C | CA | 7 | a0001c0001t0004g0074 a0001c0001t0004g0092 a0001c0001t0004g0095 others(4): Show |
7 | HG00735.hp2 HG01934.hp2 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.1276+177dupT | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 12/14 | chr12 | 51099477 | |||||||
| chr12:51099477 | CA | C | 252 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(249): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.1276+177delT | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 12/14 | chr12 | 51099477 | |||||||
| chr12:51099942 | A | G | 1 | a0001c0001t0002g0197 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1152-163T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 11/14 | chr12 | 51099942 | |||||||
| chr12:51099987 | A | T | 1 | a0001c0001t0006g0313 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1152-208T>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 11/14 | chr12 | 51099987 | |||||||
| chr12:51100582 | G | A | 3 | a0001c0001t0003g0032 a0001c0001t0003g0033 a0001c0001t0003g0049 |
3 | HG02572.hp2 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1152-803C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 11/14 | chr12 | 51100582 | |||||||
| chr12:51100600 | G | A | 6 | a0001c0001t0014g0018 a0001c0001t0014g0019 a0001c0001t0014g0020 others(3): Show |
6 | HG04228.hp2 NA18747.hp1 NA18984.hp1 others(3): Show |
intron_variant | MODIFIER | c.1152-821C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 11/14 | chr12 | 51100600 | |||||||
| chr12:51100618 | C | A | 6 | a0001c0001t0014g0018 a0001c0001t0014g0019 a0001c0001t0014g0020 others(3): Show |
6 | HG04228.hp2 NA18747.hp1 NA18984.hp1 others(3): Show |
intron_variant | MODIFIER | c.1152-839G>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 11/14 | chr12 | 51100618 | |||||||
| chr12:51100625 | G | C | 1 | a0001c0001t0001g0306 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1152-846C>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 11/14 | chr12 | 51100625 | |||||||
| chr12:51100633 | C | T | 1 | a0001c0001t0002g0181 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1152-854G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 11/14 | chr12 | 51100633 | |||||||
| chr12:51100643 | C | G | 3 | a0001c0001t0017g0199 a0001c0001t0017g0203 a0001c0001t0017g0303 |
3 | HG00140.hp1 HG02698.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1152-864G>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 11/14 | chr12 | 51100643 | |||||||
| chr12:51100657 | A | G | 79 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0138 others(76): Show |
82 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.1152-878T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 11/14 | chr12 | 51100657 | |||||||
| chr12:51100671 | C | T | 1 | a0001c0001t0003g0032 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1152-892G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 11/14 | chr12 | 51100671 | |||||||
| chr12:51100890 | A | C | 19 | a0001c0001t0005g0118 a0001c0001t0005g0119 a0001c0001t0005g0120 others(16): Show |
19 | HG01346.hp2 HG02145.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.1151+1045T>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 11/14 | chr12 | 51100890 | |||||||
| chr12:51100966 | G | A | 4 | a0001c0001t0002g0298 a0001c0001t0002g0299 a0001c0001t0002g0300 others(1): Show |
4 | HG02109.hp1 HG03471.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1151+969C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 11/14 | chr12 | 51100966 | |||||||
| chr12:51100994 | T | C | 1 | a0001c0001t0003g0025 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1151+941A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 11/14 | chr12 | 51100994 | |||||||
| chr12:51101108 | C | T | 1 | a0001c0001t0002g0156 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1151+827G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 11/14 | chr12 | 51101108 | |||||||
| chr12:51101342 | A | G | 1 | a0001c0001t0005g0120 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1151+593T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 11/14 | chr12 | 51101342 | |||||||
| chr12:51101509 | C | A | 80 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0138 others(77): Show |
83 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.1151+426G>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 11/14 | chr12 | 51101509 | |||||||
| chr12:51101772 | G | T | 1 | a0001c0001t0001g0216 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1151+163C>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 11/14 | chr12 | 51101772 | |||||||
| chr12:51101907 | T | C | 4 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 others(1): Show |
4 | HG02717.hp2 HG03041.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1151+28A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 11/14 | chr12 | 51101907 | |||||||
| chr12:51102205 | C | T | 100 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(97): Show |
103 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.1061-180G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 10/14 | chr12 | 51102205 | |||||||
| chr12:51102371 | C | T | 1 | a0001c0001t0003g0060 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1061-346G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 10/14 | chr12 | 51102371 | |||||||
| chr12:51102618 | C | T | 2 | a0001c0001t0017g0199 a0001c0001t0017g0203 |
2 | HG00140.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1061-593G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 10/14 | chr12 | 51102618 | |||||||
| chr12:51102876 | T | C | 75 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(72): Show |
76 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.1060+794A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 10/14 | chr12 | 51102876 | |||||||
| chr12:51102902 | C | CT | 19 | a0001c0001t0005g0118 a0001c0001t0005g0119 a0001c0001t0005g0120 others(16): Show |
19 | HG01346.hp2 HG02145.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.1060+767dupA | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 10/14 | chr12 | 51102902 | |||||||
| chr12:51102918 | T | C | 2 | a0001c0001t0022g0336 a0001c0001t0022g0337 |
2 | HG01070.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.1060+752A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 10/14 | chr12 | 51102918 | |||||||
| chr12:51103039 | T | C | 1 | a0001c0001t0003g0011 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1060+631A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 10/14 | chr12 | 51103039 | |||||||
| chr12:51103262 | G | A | 1 | a0001c0001t0016g0302 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1060+408C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 10/14 | chr12 | 51103262 | |||||||
| chr12:51103790 | T | C | 19 | a0001c0001t0005g0118 a0001c0001t0005g0119 a0001c0001t0005g0120 others(16): Show |
19 | HG01346.hp2 HG02145.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.967-27A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 9/14 | chr12 | 51103790 | |||||||
| chr12:51103802 | T | C | 2 | a0001c0001t0017g0199 a0001c0001t0017g0203 |
2 | HG00140.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.967-39A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 9/14 | chr12 | 51103802 | |||||||
| chr12:51104287 | T | C | 1 | a0001c0001t0002g0283 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.918-84A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 8/14 | chr12 | 51104287 | |||||||
| chr12:51104413 | A | G | 2 | a0001c0001t0022g0336 a0001c0001t0022g0337 |
2 | HG01070.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.918-210T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 8/14 | chr12 | 51104413 | |||||||
| chr12:51104428 | T | C | 54 | a0001c0001t0004g0003 a0001c0001t0004g0004 a0001c0001t0004g0005 others(51): Show |
57 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.918-225A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 8/14 | chr12 | 51104428 | |||||||
| chr12:51104697 | T | C | 1 | a0001c0001t0005g0126 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.918-494A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 8/14 | chr12 | 51104697 | |||||||
| chr12:51104713 | A | AT | 15 | a0001c0001t0001g0317 a0001c0001t0001g0318 a0001c0001t0001g0320 others(12): Show |
16 | HG01928.hp1 HG02040.hp2 HG02723.hp1 others(13): Show |
intron_variant | MODIFIER | c.918-511dupA | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 8/14 | chr12 | 51104713 | |||||||
| chr12:51104713 | AT | A | 86 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(83): Show |
89 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.918-511delA | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 8/14 | chr12 | 51104713 | |||||||
| chr12:51104735 | G | C | 1 | a0001c0001t0001g0294 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.918-532C>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 8/14 | chr12 | 51104735 | |||||||
| chr12:51104769 | C | T | 331 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(328): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.918-566G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 8/14 | chr12 | 51104769 | |||||||
| chr12:51104793 | C | G | 180 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(177): Show |
186 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.918-590G>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 8/14 | chr12 | 51104793 | |||||||
| chr12:51104878 | A | T | 75 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(72): Show |
76 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.918-675T>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 8/14 | chr12 | 51104878 | |||||||
| chr12:51104952 | T | C | 1 | a0001c0001t0002g0156 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.918-749A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 8/14 | chr12 | 51104952 | |||||||
| chr12:51104954 | C | T | 1 | a0001c0001t0002g0171 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.918-751G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 8/14 | chr12 | 51104954 | |||||||
| chr12:51104992 | G | A | 1 | a0001c0001t0002g0173 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.918-789C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 8/14 | chr12 | 51104992 | |||||||
| chr12:51105044 | T | C | 4 | a0001c0001t0002g0298 a0001c0001t0002g0299 a0001c0001t0002g0300 others(1): Show |
4 | HG02109.hp1 HG03471.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.918-841A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 8/14 | chr12 | 51105044 | |||||||
| chr12:51105146 | C | T | 9 | a0001c0001t0006g0309 a0001c0001t0006g0310 a0001c0001t0006g0312 others(6): Show |
9 | HG02145.hp2 HG02559.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.918-943G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 8/14 | chr12 | 51105146 | |||||||
| chr12:51105154 | CATG | C | 51 | a0001c0001t0003g0002 a0001c0001t0003g0010 a0001c0001t0003g0011 others(48): Show |
52 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.918-954_918-952del others(3): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 8/14 | chr12 | 51105154 | |||||||
| chr12:51105313 | C | G | 3 | a0001c0001t0006g0200 a0001c0001t0006g0201 a0001c0001t0006g0202 |
3 | HG02976.hp1 HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.918-1110G>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 8/14 | chr12 | 51105313 | |||||||
| chr12:51105327 | C | G | 6 | a0001c0001t0001g0317 a0001c0001t0001g0318 a0001c0001t0001g0319 others(3): Show |
6 | HG01884.hp2 HG02723.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.918-1124G>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 8/14 | chr12 | 51105327 | |||||||
| chr12:51105394 | T | A | 1 | a0001c0001t0008g0116 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.917+1131A>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 8/14 | chr12 | 51105394 | |||||||
| chr12:51105472 | G | A | 79 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0138 others(76): Show |
82 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.917+1053C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 8/14 | chr12 | 51105472 | |||||||
| chr12:51105936 | T | C | 74 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(71): Show |
75 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.917+589A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 8/14 | chr12 | 51105936 | |||||||
| chr12:51105961 | T | C | 1 | a0001c0001t0002g0311 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.917+564A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 8/14 | chr12 | 51105961 | |||||||
| chr12:51106022 | C | T | 1 | a0001c0001t0009g0093 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.917+503G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 8/14 | chr12 | 51106022 | |||||||
| chr12:51106072 | A | C | 7 | a0001c0001t0001g0151 a0001c0001t0001g0234 a0001c0001t0001g0256 others(4): Show |
7 | HG00438.hp1 HG03669.hp1 HG04184.hp2 others(4): Show |
intron_variant | MODIFIER | c.917+453T>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 8/14 | chr12 | 51106072 | |||||||
| chr12:51106189 | A | G | 2 | a0001c0001t0001g0151 a0001c0001t0001g0261 |
2 | NA19012.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.917+336T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 8/14 | chr12 | 51106189 | |||||||
| chr12:51106197 | A | G | 1 | a0001c0001t0001g0215 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.917+328T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 8/14 | chr12 | 51106197 | |||||||
| chr12:51106297 | A | G | 1 | a0001c0001t0017g0303 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.917+228T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 8/14 | chr12 | 51106297 | |||||||
| chr12:51106701 | G | A | 5 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(2): Show |
5 | HG02451.hp2 HG02886.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.829-88C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 7/14 | chr12 | 51106701 | |||||||
| chr12:51106921 | C | T | 6 | a0001c0001t0001g0317 a0001c0001t0001g0318 a0001c0001t0001g0319 others(3): Show |
6 | HG01884.hp2 HG02723.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.829-308G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 7/14 | chr12 | 51106921 | |||||||
| chr12:51107103 | G | T | 78 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(75): Show |
80 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.828+133C>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 7/14 | chr12 | 51107103 | |||||||
| chr12:51107540 | T | C | 1 | a0001c0002t0004g0071 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.718-194A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 6/14 | chr12 | 51107540 | |||||||
| chr12:51107560 | G | T | 53 | a0001c0001t0004g0003 a0001c0001t0004g0004 a0001c0001t0004g0005 others(50): Show |
56 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.718-214C>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 6/14 | chr12 | 51107560 | |||||||
| chr12:51107629 | C | T | 53 | a0001c0001t0003g0002 a0001c0001t0003g0010 a0001c0001t0003g0011 others(50): Show |
55 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.718-283G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 6/14 | chr12 | 51107629 | |||||||
| chr12:51107678 | C | T | 1 | a0001c0001t0017g0303 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.718-332G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 6/14 | chr12 | 51107678 | |||||||
| chr12:51107751 | C | T | 80 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0138 others(77): Show |
83 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.718-405G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 6/14 | chr12 | 51107751 | |||||||
| chr12:51107752 | G | A | 1 | a0001c0001t0001g0308 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.718-406C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 6/14 | chr12 | 51107752 | |||||||
| chr12:51107820 | G | A | 5 | a0001c0001t0001g0145 a0001c0001t0001g0164 a0001c0001t0001g0212 others(2): Show |
5 | HG01891.hp1 HG02055.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.718-474C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 6/14 | chr12 | 51107820 | |||||||
| chr12:51107856 | G | A | 1 | a0001c0001t0001g0306 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.718-510C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 6/14 | chr12 | 51107856 | |||||||
| chr12:51107994 | A | C | 7 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(4): Show |
7 | HG02451.hp2 HG02630.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.718-648T>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 6/14 | chr12 | 51107994 | |||||||
| chr12:51108050 | C | T | 8 | a0001c0001t0014g0018 a0001c0001t0014g0019 a0001c0001t0014g0020 others(5): Show |
8 | HG00140.hp1 HG02698.hp2 HG04228.hp2 others(5): Show |
intron_variant | MODIFIER | c.718-704G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 6/14 | chr12 | 51108050 | |||||||
| chr12:51108106 | G | A | 1 | a0001c0001t0002g0254 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.718-760C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 6/14 | chr12 | 51108106 | |||||||
| chr12:51108262 | G | T | 2 | a0001c0001t0017g0199 a0001c0001t0017g0203 |
2 | HG00140.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.717+859C>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 6/14 | chr12 | 51108262 | |||||||
| chr12:51108373 | G | T | 3 | a0001c0001t0002g0175 a0001c0001t0002g0184 a0001c0001t0002g0185 |
3 | HG01175.hp2 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.717+748C>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 6/14 | chr12 | 51108373 | |||||||
| chr12:51108576 | C | T | 1 | a0001c0001t0001g0306 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.717+545G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 6/14 | chr12 | 51108576 | |||||||
| chr12:51108668 | G | A | 1 | a0001c0001t0017g0303 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.717+453C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 6/14 | chr12 | 51108668 | |||||||
| chr12:51108686 | A | G | 6 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(3): Show |
6 | HG00597.hp1 HG02056.hp1 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.717+435T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 6/14 | chr12 | 51108686 | |||||||
| chr12:51108764 | A | AAAAT | 10 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 others(7): Show |
10 | HG01884.hp2 HG02717.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.717+353_717+356dup others(4): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 6/14 | chr12 | 51108764 | |||||||
| chr12:51108802 | G | T | 2 | a0001c0001t0001g0213 a0001c0001t0001g0245 |
2 | NA18971.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.717+319C>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 6/14 | chr12 | 51108802 | |||||||
| chr12:51108941 | C | T | 2 | a0001c0001t0017g0199 a0001c0001t0017g0203 |
2 | HG00140.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.717+180G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 6/14 | chr12 | 51108941 | |||||||
| chr12:51109008 | C | T | 188 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(185): Show |
194 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.717+113G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 6/14 | chr12 | 51109008 | |||||||
| chr12:51109048 | G | C | 1 | a0001c0001t0004g0112 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.717+73C>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 6/14 | chr12 | 51109048 | |||||||
| chr12:51109354 | A | G | 54 | a0001c0001t0004g0003 a0001c0001t0004g0004 a0001c0001t0004g0005 others(51): Show |
57 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.565-81T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 5/14 | chr12 | 51109354 | |||||||
| chr12:51109522 | C | T | 1 | a0001c0001t0016g0302 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.565-249G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 5/14 | chr12 | 51109522 | |||||||
| chr12:51109541 | C | T | 1 | a0001c0001t0001g0296 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.565-268G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 5/14 | chr12 | 51109541 | |||||||
| chr12:51109658 | C | T | 34 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0150 others(31): Show |
37 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.565-385G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 5/14 | chr12 | 51109658 | |||||||
| chr12:51109659 | A | G | 79 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0138 others(76): Show |
82 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.565-386T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 5/14 | chr12 | 51109659 | |||||||
| chr12:51109715 | AT | A | 131 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(128): Show |
133 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.565-443delA | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 5/14 | chr12 | 51109715 | |||||||
| chr12:51109715 | ATT | A | 81 | a0001c0001t0001g0164 a0001c0001t0001g0238 a0001c0001t0001g0275 others(78): Show |
85 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.565-444_565-443del others(2): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 5/14 | chr12 | 51109715 | |||||||
| chr12:51109715 | ATTT | A | 45 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(42): Show |
45 | HG01069.hp2 HG01081.hp1 HG01346.hp2 others(42): Show |
intron_variant | MODIFIER | c.565-445_565-443del others(3): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 5/14 | chr12 | 51109715 | |||||||
| chr12:51109715 | ATTTT | A | 55 | a0001c0001t0001g0141 a0001c0001t0004g0003 a0001c0001t0004g0004 others(52): Show |
58 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.565-446_565-443del others(4): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 5/14 | chr12 | 51109715 | |||||||
| chr12:51109728 | T | C | 1 | a0001c0001t0006g0316 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.565-455A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 5/14 | chr12 | 51109728 | |||||||
| chr12:51109788 | G | A | 2 | a0001c0001t0002g0170 a0001c0001t0002g0171 |
2 | HG02683.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.565-515C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 5/14 | chr12 | 51109788 | |||||||
| chr12:51109848 | A | G | 7 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(4): Show |
7 | HG02451.hp2 HG02630.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.565-575T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 5/14 | chr12 | 51109848 | |||||||
| chr12:51110238 | T | C | 1 | a0001c0001t0001g0231 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.564+639A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 5/14 | chr12 | 51110238 | |||||||
| chr12:51110389 | C | T | 97 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(94): Show |
100 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.564+488G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 5/14 | chr12 | 51110389 | |||||||
| chr12:51110573 | C | A | 327 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(324): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.564+304G>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 5/14 | chr12 | 51110573 | |||||||
| chr12:51110734 | G | A | 1 | a0001c0001t0002g0280 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.564+143C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 5/14 | chr12 | 51110734 | |||||||
| chr12:51111016 | T | C | 319 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(316): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.458-33A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51111016 | |||||||
| chr12:51111111 | GT | G | 261 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(258): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.458-129delA | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51111111 | |||||||
| chr12:51111127 | G | A | 1 | a0001c0001t0001g0308 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.458-144C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51111127 | |||||||
| chr12:51111553 | C | T | 75 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(72): Show |
76 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.458-570G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51111553 | |||||||
| chr12:51111584 | G | A | 51 | a0001c0001t0003g0002 a0001c0001t0003g0010 a0001c0001t0003g0011 others(48): Show |
52 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.458-601C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51111584 | |||||||
| chr12:51111631 | G | A | 1 | a0001c0001t0005g0134 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.458-648C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51111631 | |||||||
| chr12:51111786 | G | A | 4 | a0001c0001t0002g0298 a0001c0001t0002g0299 a0001c0001t0002g0300 others(1): Show |
4 | HG02109.hp1 HG03471.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.458-803C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51111786 | |||||||
| chr12:51111802 | C | T | 1 | a0001c0001t0002g0191 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.458-819G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51111802 | |||||||
| chr12:51111851 | T | C | 1 | a0001c0001t0001g0305 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.458-868A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51111851 | |||||||
| chr12:51112115 | C | T | 53 | a0001c0001t0003g0002 a0001c0001t0003g0010 a0001c0001t0003g0011 others(50): Show |
55 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.458-1132G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51112115 | |||||||
| chr12:51112120 | C | T | 263 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(260): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.458-1137G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51112120 | |||||||
| chr12:51112494 | A | G | 6 | a0001c0001t0014g0018 a0001c0001t0014g0019 a0001c0001t0014g0020 others(3): Show |
6 | HG04228.hp2 NA18747.hp1 NA18984.hp1 others(3): Show |
intron_variant | MODIFIER | c.458-1511T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51112494 | |||||||
| chr12:51112523 | G | A | 1 | a0001c0001t0004g0102 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.458-1540C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51112523 | |||||||
| chr12:51112545 | T | C | 263 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(260): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.458-1562A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51112545 | |||||||
| chr12:51112604 | C | T | 5 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(2): Show |
5 | HG02451.hp2 HG02886.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.458-1621G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51112604 | |||||||
| chr12:51112810 | T | A | 75 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(72): Show |
76 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.458-1827A>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51112810 | |||||||
| chr12:51112866 | C | CA | 84 | a0001c0001t0001g0216 a0001c0001t0002g0001 a0001c0001t0002g0007 others(81): Show |
87 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.458-1884dupT | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51112866 | |||||||
| chr12:51112866 | CA | C | 56 | a0001c0001t0001g0151 a0001c0001t0001g0261 a0001c0001t0004g0003 others(53): Show |
59 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.458-1884delT | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51112866 | |||||||
| chr12:51113089 | T | A | 4 | a0001c0001t0002g0298 a0001c0001t0002g0299 a0001c0001t0002g0300 others(1): Show |
4 | HG02109.hp1 HG03471.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.458-2106A>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51113089 | |||||||
| chr12:51113091 | T | TA | 4 | a0001c0001t0002g0298 a0001c0001t0002g0299 a0001c0001t0002g0300 others(1): Show |
4 | HG02109.hp1 HG03471.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.458-2109_458-2108i others(3): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51113091 | |||||||
| chr12:51113092 | G | T | 4 | a0001c0001t0002g0298 a0001c0001t0002g0299 a0001c0001t0002g0300 others(1): Show |
4 | HG02109.hp1 HG03471.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.458-2109C>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51113092 | |||||||
| chr12:51113093 | G | A | 82 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(79): Show |
84 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.458-2110C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51113093 | |||||||
| chr12:51113232 | C | A | 4 | a0001c0001t0002g0298 a0001c0001t0002g0299 a0001c0001t0002g0300 others(1): Show |
4 | HG02109.hp1 HG03471.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.458-2249G>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51113232 | |||||||
| chr12:51113330 | C | T | 331 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(328): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.458-2347G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51113330 | |||||||
| chr12:51113494 | G | A | 6 | a0001c0001t0001g0317 a0001c0001t0001g0318 a0001c0001t0001g0319 others(3): Show |
6 | HG01884.hp2 HG02723.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.458-2511C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51113494 | |||||||
| chr12:51113579 | T | G | 2 | a0001c0001t0004g0110 a0001c0001t0004g0114 |
2 | NA18946.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.458-2596A>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51113579 | |||||||
| chr12:51113627 | T | G | 334 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(331): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.458-2644A>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51113627 | |||||||
| chr12:51113641 | G | A | 27 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(24): Show |
27 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.458-2658C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51113641 | |||||||
| chr12:51113676 | A | G | 6 | a0001c0001t0014g0018 a0001c0001t0014g0019 a0001c0001t0014g0020 others(3): Show |
6 | HG04228.hp2 NA18747.hp1 NA18984.hp1 others(3): Show |
intron_variant | MODIFIER | c.457+2639T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51113676 | |||||||
| chr12:51113846 | C | A | 1 | a0001c0001t0025g0086 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.457+2469G>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51113846 | |||||||
| chr12:51113851 | T | G | 75 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(72): Show |
76 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.457+2464A>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51113851 | |||||||
| chr12:51114056 | C | A | 2 | a0001c0001t0002g0167 a0001c0001t0002g0172 |
2 | HG00099.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.457+2259G>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51114056 | |||||||
| chr12:51114208 | T | C | 6 | a0001c0001t0014g0018 a0001c0001t0014g0019 a0001c0001t0014g0020 others(3): Show |
6 | HG04228.hp2 NA18747.hp1 NA18984.hp1 others(3): Show |
intron_variant | MODIFIER | c.457+2107A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51114208 | |||||||
| chr12:51114267 | C | T | 87 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(84): Show |
89 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.457+2048G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51114267 | |||||||
| chr12:51114290 | C | T | 266 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(263): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.457+2025G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51114290 | |||||||
| chr12:51114508 | G | A | 1 | a0001c0001t0010g0198 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.457+1807C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51114508 | |||||||
| chr12:51114623 | A | G | 75 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(72): Show |
76 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.457+1692T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51114623 | |||||||
| chr12:51114748 | C | G | 12 | a0001c0001t0004g0077 a0001c0001t0004g0082 a0001c0001t0004g0084 others(9): Show |
12 | HG00423.hp2 HG00642.hp2 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.457+1567G>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51114748 | |||||||
| chr12:51114802 | G | A | 1 | a0001c0001t0002g0166 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.457+1513C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51114802 | |||||||
| chr12:51114830 | G | A | 1 | a0001c0001t0017g0303 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.457+1485C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51114830 | |||||||
| chr12:51114856 | G | A | 1 | a0001c0001t0002g0324 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.457+1459C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51114856 | |||||||
| chr12:51114972 | A | G | 179 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(176): Show |
185 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.457+1343T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51114972 | |||||||
| chr12:51114992 | G | C | 334 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(331): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.457+1323C>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51114992 | |||||||
| chr12:51115016 | G | A | 11 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0121 others(8): Show |
11 | HG01346.hp2 HG02145.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.457+1299C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51115016 | |||||||
| chr12:51115048 | C | G | 6 | a0001c0001t0014g0018 a0001c0001t0014g0019 a0001c0001t0014g0020 others(3): Show |
6 | HG04228.hp2 NA18747.hp1 NA18984.hp1 others(3): Show |
intron_variant | MODIFIER | c.457+1267G>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51115048 | |||||||
| chr12:51115064 | G | GAAAAAAA others(1): Show |
22 | a0001c0001t0001g0240 a0001c0001t0002g0180 a0001c0001t0005g0118 others(19): Show |
22 | HG00140.hp1 HG00735.hp1 HG01346.hp2 others(19): Show |
intron_variant | MODIFIER | c.457+1243_457+1250d others(10): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51115064 | |||||||
| chr12:51115064 | G | GAAAAAAA others(2): Show |
222 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(219): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.457+1242_457+1250d others(11): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51115064 | |||||||
| chr12:51115064 | G | GAAAAAAA others(3): Show |
64 | a0001c0001t0001g0227 a0001c0001t0001g0236 a0001c0001t0001g0248 others(61): Show |
66 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.457+1241_457+1250d others(12): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51115064 | |||||||
| chr12:51115064 | G | GAAAAAAA others(4): Show |
8 | a0001c0001t0003g0011 a0001c0001t0003g0016 a0001c0001t0003g0035 others(5): Show |
8 | HG01346.hp1 HG01884.hp1 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.457+1240_457+1250d others(13): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51115064 | |||||||
| chr12:51115064 | G | GAAAAAAA others(5): Show |
1 | a0001c0001t0003g0055 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.457+1239_457+1250d others(14): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51115064 | |||||||
| chr12:51115119 | C | CT | 16 | a0001c0001t0001g0231 a0001c0001t0001g0248 a0001c0001t0001g0257 others(13): Show |
16 | HG01106.hp2 HG01175.hp1 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.457+1195dupA | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51115119 | |||||||
| chr12:51115119 | CT | C | 154 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(151): Show |
160 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.457+1195delA | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51115119 | |||||||
| chr12:51115276 | C | T | 4 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(1): Show |
4 | HG02451.hp2 HG02886.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.457+1039G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51115276 | |||||||
| chr12:51115311 | G | A | 1 | a0001c0001t0022g0337 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.457+1004C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51115311 | |||||||
| chr12:51115408 | T | C | 1 | a0001c0001t0003g0014 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.457+907A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51115408 | |||||||
| chr12:51115409 | C | T | 1 | a0001c0001t0003g0014 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.457+906G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51115409 | |||||||
| chr12:51115412 | G | A | 60 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(57): Show |
64 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.457+903C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51115412 | |||||||
| chr12:51115505 | C | G | 2 | a0001c0001t0004g0078 a0001c0001t0004g0079 |
2 | HG02129.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.457+810G>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51115505 | |||||||
| chr12:51115704 | G | A | 65 | a0001c0001t0003g0002 a0001c0001t0003g0010 a0001c0001t0003g0011 others(62): Show |
67 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.457+611C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51115704 | |||||||
| chr12:51116067 | C | T | 1 | a0001c0001t0003g0057 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.457+248G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51116067 | |||||||
| chr12:51116101 | T | C | 6 | a0001c0001t0014g0018 a0001c0001t0014g0019 a0001c0001t0014g0020 others(3): Show |
6 | HG04228.hp2 NA18747.hp1 NA18984.hp1 others(3): Show |
intron_variant | MODIFIER | c.457+214A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51116101 | |||||||
| chr12:51116297 | T | C | 2 | a0001c0001t0017g0199 a0001c0001t0017g0203 |
2 | HG00140.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.457+18A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 4/14 | chr12 | 51116297 | |||||||
| chr12:51116451 | C | A | 53 | a0001c0001t0003g0002 a0001c0001t0003g0010 a0001c0001t0003g0011 others(50): Show |
55 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.352-31G>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 3/14 | chr12 | 51116451 | |||||||
| chr12:51116620 | C | CT | 53 | a0001c0001t0001g0229 a0001c0001t0003g0002 a0001c0001t0003g0010 others(50): Show |
55 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.352-201dupA | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 3/14 | chr12 | 51116620 | |||||||
| chr12:51116620 | CT | C | 23 | a0001c0001t0001g0145 a0001c0001t0001g0164 a0001c0001t0001g0212 others(20): Show |
23 | HG00140.hp1 HG01069.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.352-201delA | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 3/14 | chr12 | 51116620 | |||||||
| chr12:51116651 | C | T | 1 | a0001c0001t0004g0074 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.352-231G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 3/14 | chr12 | 51116651 | |||||||
| chr12:51116774 | C | T | 5 | a0001c0001t0001g0317 a0001c0001t0001g0318 a0001c0001t0001g0319 others(2): Show |
5 | HG01884.hp2 HG02970.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.352-354G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 3/14 | chr12 | 51116774 | |||||||
| chr12:51116859 | C | T | 75 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(72): Show |
76 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.352-439G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 3/14 | chr12 | 51116859 | |||||||
| chr12:51116883 | C | A | 1 | a0001c0001t0001g0305 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.352-463G>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 3/14 | chr12 | 51116883 | |||||||
| chr12:51116897 | G | A | 1 | a0001c0001t0022g0337 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.352-477C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 3/14 | chr12 | 51116897 | |||||||
| chr12:51117030 | A | G | 125 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(122): Show |
128 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(125): Show |
intron_variant | MODIFIER | c.352-610T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 3/14 | chr12 | 51117030 | |||||||
| chr12:51117214 | C | T | 1 | a0001c0001t0001g0250 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.351+457G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 3/14 | chr12 | 51117214 | |||||||
| chr12:51117369 | G | A | 65 | a0001c0001t0003g0002 a0001c0001t0003g0010 a0001c0001t0003g0011 others(62): Show |
67 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.351+302C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 3/14 | chr12 | 51117369 | |||||||
| chr12:51117393 | C | A | 6 | a0001c0001t0001g0145 a0001c0001t0001g0164 a0001c0001t0001g0212 others(3): Show |
6 | HG01891.hp1 HG02055.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.351+278G>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 3/14 | chr12 | 51117393 | |||||||
| chr12:51117460 | T | G | 57 | a0001c0001t0004g0003 a0001c0001t0004g0004 a0001c0001t0004g0005 others(54): Show |
61 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.351+211A>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 3/14 | chr12 | 51117460 | |||||||
| chr12:51117461 | G | A | 125 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(122): Show |
128 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(125): Show |
intron_variant | MODIFIER | c.351+210C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 3/14 | chr12 | 51117461 | |||||||
| chr12:51117481 | T | C | 51 | a0001c0001t0003g0002 a0001c0001t0003g0010 a0001c0001t0003g0011 others(48): Show |
52 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.351+190A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 3/14 | chr12 | 51117481 | |||||||
| chr12:51117486 | A | G | 19 | a0001c0001t0005g0118 a0001c0001t0005g0119 a0001c0001t0005g0120 others(16): Show |
19 | HG01346.hp2 HG02145.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.351+185T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 3/14 | chr12 | 51117486 | |||||||
| chr12:51117639 | T | A | 1 | a0001c0001t0002g0195 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.351+32A>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 3/14 | chr12 | 51117639 | |||||||
| chr12:51117826 | T | G | 1 | a0001c0001t0002g0178 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.275-79A>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 2/14 | chr12 | 51117826 | |||||||
| chr12:51117920 | T | C | 1 | a0001c0001t0005g0133 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.275-173A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 2/14 | chr12 | 51117920 | |||||||
| chr12:51117945 | T | C | 9 | a0001c0001t0006g0309 a0001c0001t0006g0310 a0001c0001t0006g0312 others(6): Show |
9 | HG02145.hp2 HG02559.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.275-198A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 2/14 | chr12 | 51117945 | |||||||
| chr12:51117962 | C | G | 141 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(138): Show |
146 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.275-215G>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 2/14 | chr12 | 51117962 | |||||||
| chr12:51118110 | A | C | 1 | a0001c0001t0001g0272 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.275-363T>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 2/14 | chr12 | 51118110 | |||||||
| chr12:51118121 | T | C | 1 | a0001c0001t0001g0144 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.275-374A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 2/14 | chr12 | 51118121 | |||||||
| chr12:51118176 | G | A | 1 | a0001c0001t0002g0173 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.275-429C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 2/14 | chr12 | 51118176 | |||||||
| chr12:51118186 | C | A | 3 | a0001c0001t0013g0006 a0001c0001t0013g0155 a0001c0001t0013g0297 |
4 | HG02723.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.274+435G>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 2/14 | chr12 | 51118186 | |||||||
| chr12:51118276 | C | T | 1 | a0001c0001t0002g0007 | 2 | HG00140.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.274+345G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 2/14 | chr12 | 51118276 | |||||||
| chr12:51118332 | A | C | 3 | a0001c0001t0001g0152 a0001c0001t0001g0225 a0001c0001t0001g0232 |
3 | HG00099.hp2 HG01167.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.274+289T>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 2/14 | chr12 | 51118332 | |||||||
| chr12:51118447 | C | T | 81 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0138 others(78): Show |
84 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.274+174G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 2/14 | chr12 | 51118447 | |||||||
| chr12:51118854 | CT | C | 125 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(122): Show |
128 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(125): Show |
intron_variant | MODIFIER | c.123-83delA | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51118854 | |||||||
| chr12:51119011 | A | G | 2 | a0001c0001t0024g0066 a0001c0001t0032g0334 |
2 | HG02630.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.123-239T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51119011 | |||||||
| chr12:51119056 | A | T | 5 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(2): Show |
5 | HG02451.hp2 HG02886.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.123-284T>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51119056 | |||||||
| chr12:51119092 | G | A | 1 | a0001c0001t0001g0325 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.123-320C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51119092 | |||||||
| chr12:51119154 | T | C | 1 | a0001c0001t0001g0211 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.123-382A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51119154 | |||||||
| chr12:51119452 | T | C | 2 | a0001c0001t0003g0028 a0001c0001t0003g0052 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.123-680A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51119452 | |||||||
| chr12:51119468 | C | T | 2 | a0001c0001t0001g0305 a0001c0001t0001g0306 |
2 | HG02258.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.123-696G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51119468 | |||||||
| chr12:51119526 | G | A | 1 | a0001c0001t0002g0327 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.123-754C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51119526 | |||||||
| chr12:51119539 | T | C | 132 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(129): Show |
137 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.123-767A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51119539 | |||||||
| chr12:51119541 | C | T | 1 | a0001c0001t0001g0292 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.123-769G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51119541 | |||||||
| chr12:51119572 | G | A | 121 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(118): Show |
124 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(121): Show |
intron_variant | MODIFIER | c.123-800C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51119572 | |||||||
| chr12:51119642 | C | T | 2 | a0001c0001t0003g0010 a0001c0001t0003g0011 |
2 | HG01081.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.123-870G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51119642 | |||||||
| chr12:51119653 | G | A | 1 | a0001c0001t0021g0289 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.123-881C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51119653 | |||||||
| chr12:51119825 | G | A | 75 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(72): Show |
76 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.123-1053C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51119825 | |||||||
| chr12:51120127 | G | A | 3 | a0001c0001t0013g0006 a0001c0001t0013g0155 a0001c0001t0013g0297 |
4 | HG02723.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-1355C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51120127 | |||||||
| chr12:51120177 | C | CA | 6 | a0001c0001t0001g0216 a0001c0001t0001g0243 a0001c0001t0001g0263 others(3): Show |
6 | HG01109.hp2 HG02083.hp2 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.123-1406dupT | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51120177 | |||||||
| chr12:51120177 | CA | C | 137 | a0001c0001t0001g0145 a0001c0001t0001g0164 a0001c0001t0001g0208 others(134): Show |
141 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.123-1406delT | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51120177 | |||||||
| chr12:51120177 | CAA | C | 110 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(107): Show |
114 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(111): Show |
intron_variant | MODIFIER | c.123-1407_123-1406d others(4): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51120177 | |||||||
| chr12:51120177 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0152 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.123-1416_123-1406d others(13): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51120177 | |||||||
| chr12:51120192 | A | G | 1 | a0001c0001t0002g0156 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.123-1420T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51120192 | |||||||
| chr12:51120202 | G | C | 4 | a0001c0001t0001g0145 a0001c0001t0001g0164 a0001c0001t0001g0212 others(1): Show |
4 | HG01891.hp1 HG02055.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-1430C>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51120202 | |||||||
| chr12:51120217 | C | A | 173 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(170): Show |
178 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.123-1445G>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51120217 | |||||||
| chr12:51120331 | A | G | 1 | a0001c0001t0005g0120 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.123-1559T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51120331 | |||||||
| chr12:51120545 | G | GT | 4 | a0001c0001t0002g0298 a0001c0001t0002g0299 a0001c0001t0002g0300 others(1): Show |
4 | HG02109.hp1 HG03471.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-1774dupA | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51120545 | |||||||
| chr12:51120569 | T | C | 75 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(72): Show |
76 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.123-1797A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51120569 | |||||||
| chr12:51120859 | G | A | 1 | a0001c0001t0001g0295 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.123-2087C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51120859 | |||||||
| chr12:51120909 | C | CA | 61 | a0001c0001t0001g0145 a0001c0001t0001g0212 a0001c0001t0001g0292 others(58): Show |
62 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.123-2138dupT | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51120909 | |||||||
| chr12:51120909 | C | CAA | 85 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(82): Show |
88 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.123-2139_123-2138d others(4): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51120909 | |||||||
| chr12:51120909 | C | CAAA | 56 | a0001c0001t0001g0218 a0001c0001t0001g0230 a0001c0001t0001g0231 others(53): Show |
59 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.123-2140_123-2138d others(5): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51120909 | |||||||
| chr12:51121041 | A | T | 2 | a0001c0001t0001g0210 a0001c0001t0001g0220 |
2 | HG03834.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.123-2269T>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51121041 | |||||||
| chr12:51121046 | AG | A | 71 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(68): Show |
72 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.123-2275delC | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51121046 | |||||||
| chr12:51121047 | G | A | 3 | a0001c0001t0001g0207 a0001c0001t0001g0219 a0001c0001t0001g0247 |
3 | HG03654.hp1 NA18962.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.123-2275C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51121047 | |||||||
| chr12:51121052 | A | T | 2 | a0001c0001t0001g0207 a0001c0001t0001g0247 |
2 | NA18962.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.123-2280T>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51121052 | |||||||
| chr12:51121293 | C | T | 1 | a0001c0001t0002g0173 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.123-2521G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51121293 | |||||||
| chr12:51121394 | G | A | 1 | a0001c0001t0006g0201 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.123-2622C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51121394 | |||||||
| chr12:51121469 | A | AT | 131 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0138 others(128): Show |
137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.123-2698dupA | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51121469 | |||||||
| chr12:51121469 | AT | A | 53 | a0001c0001t0003g0002 a0001c0001t0003g0010 a0001c0001t0003g0011 others(50): Show |
55 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.123-2698delA | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51121469 | |||||||
| chr12:51121522 | G | A | 6 | a0001c0001t0014g0018 a0001c0001t0014g0019 a0001c0001t0014g0020 others(3): Show |
6 | HG04228.hp2 NA18747.hp1 NA18984.hp1 others(3): Show |
intron_variant | MODIFIER | c.123-2750C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51121522 | |||||||
| chr12:51121529 | G | A | 72 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(69): Show |
73 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.123-2757C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51121529 | |||||||
| chr12:51121592 | A | G | 1 | a0001c0001t0001g0147 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.123-2820T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51121592 | |||||||
| chr12:51121615 | G | A | 8 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0001g0317 others(5): Show |
8 | HG01884.hp2 HG02258.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.123-2843C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51121615 | |||||||
| chr12:51121654 | C | T | 335 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(332): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.123-2882G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51121654 | |||||||
| chr12:51121791 | T | A | 1 | a0001c0001t0003g0010 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.123-3019A>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51121791 | |||||||
| chr12:51121819 | T | C | 2 | a0001c0001t0002g0304 a0001c0001t0002g0307 |
2 | HG02622.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.123-3047A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51121819 | |||||||
| chr12:51122006 | T | G | 2 | a0001c0001t0005g0123 a0001c0001t0019g0053 |
2 | HG03239.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.123-3234A>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51122006 | |||||||
| chr12:51122253 | C | CT | 25 | a0001c0001t0001g0227 a0001c0001t0001g0229 a0001c0001t0001g0256 others(22): Show |
25 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(22): Show |
intron_variant | MODIFIER | c.123-3482dupA | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51122253 | |||||||
| chr12:51122253 | CT | C | 106 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0145 others(103): Show |
111 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(108): Show |
intron_variant | MODIFIER | c.123-3482delA | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51122253 | |||||||
| chr12:51122253 | CTT | C | 7 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0293 others(4): Show |
7 | HG02717.hp2 HG02886.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.123-3483_123-3482d others(4): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51122253 | |||||||
| chr12:51122288 | T | C | 2 | a0001c0001t0018g0009 a0001c0001t0018g0335 |
3 | HG01069.hp1 HG01071.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.123-3516A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51122288 | |||||||
| chr12:51122322 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.123-3550G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51122322 | |||||||
| chr12:51122614 | G | C | 2 | a0001c0001t0017g0199 a0001c0001t0017g0203 |
2 | HG00140.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.123-3842C>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51122614 | |||||||
| chr12:51122671 | A | C | 5 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 others(2): Show |
5 | HG02717.hp2 HG03041.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.123-3899T>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51122671 | |||||||
| chr12:51123095 | T | C | 1 | a0001c0001t0008g0132 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.123-4323A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51123095 | |||||||
| chr12:51123318 | G | A | 1 | a0001c0001t0022g0337 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.123-4546C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51123318 | |||||||
| chr12:51123538 | T | A | 1 | a0001c0001t0007g0270 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.123-4766A>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51123538 | |||||||
| chr12:51123575 | G | T | 53 | a0001c0001t0003g0002 a0001c0001t0003g0010 a0001c0001t0003g0011 others(50): Show |
55 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.123-4803C>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51123575 | |||||||
| chr12:51123846 | C | T | 2 | a0001c0001t0020g0029 a0001c0001t0020g0046 |
2 | HG03654.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.123-5074G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51123846 | |||||||
| chr12:51123874 | G | A | 53 | a0001c0001t0004g0003 a0001c0001t0004g0004 a0001c0001t0004g0005 others(50): Show |
56 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.123-5102C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51123874 | |||||||
| chr12:51123927 | C | T | 51 | a0001c0001t0003g0002 a0001c0001t0003g0010 a0001c0001t0003g0011 others(48): Show |
52 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.123-5155G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51123927 | |||||||
| chr12:51124098 | C | CT | 274 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(271): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.123-5327dupA | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51124098 | |||||||
| chr12:51124333 | C | A | 1 | a0001c0001t0001g0255 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.123-5561G>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51124333 | |||||||
| chr12:51124588 | G | A | 1 | a0001c0001t0002g0285 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.123-5816C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51124588 | |||||||
| chr12:51124618 | G | A | 8 | a0001c0001t0006g0309 a0001c0001t0006g0310 a0001c0001t0006g0312 others(5): Show |
8 | HG02145.hp2 HG02559.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.123-5846C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51124618 | |||||||
| chr12:51124619 | G | A | 1 | a0001c0001t0002g0284 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.123-5847C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51124619 | |||||||
| chr12:51124636 | C | T | 1 | a0001c0001t0002g0194 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.123-5864G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51124636 | |||||||
| chr12:51124752 | GCCTTTTT others(11): Show |
G | 6 | a0001c0001t0014g0018 a0001c0001t0014g0019 a0001c0001t0014g0020 others(3): Show |
6 | HG04228.hp2 NA18747.hp1 NA18984.hp1 others(3): Show |
intron_variant | MODIFIER | c.123-5998_123-5981d others(20): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51124752 | |||||||
| chr12:51124757 | T | C | 1 | a0001c0001t0003g0033 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.123-5985A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51124757 | |||||||
| chr12:51124813 | C | G | 4 | a0001c0001t0002g0298 a0001c0001t0002g0299 a0001c0001t0002g0300 others(1): Show |
4 | HG02109.hp1 HG03471.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-6041G>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51124813 | |||||||
| chr12:51125004 | C | G | 130 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(127): Show |
134 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.123-6232G>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51125004 | |||||||
| chr12:51125055 | G | A | 1 | a0001c0001t0005g0126 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.123-6283C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51125055 | |||||||
| chr12:51125323 | A | G | 85 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(82): Show |
86 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.123-6551T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51125323 | |||||||
| chr12:51125381 | C | T | 4 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(1): Show |
4 | HG02451.hp2 HG02886.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-6609G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51125381 | |||||||
| chr12:51125393 | C | G | 1 | a0001c0001t0016g0302 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.123-6621G>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51125393 | |||||||
| chr12:51125416 | C | T | 1 | a0001c0001t0001g0262 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.123-6644G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51125416 | |||||||
| chr12:51125507 | G | A | 268 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(265): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.123-6735C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51125507 | |||||||
| chr12:51125630 | T | G | 3 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0264 |
3 | HG00423.hp1 HG02040.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.123-6858A>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51125630 | |||||||
| chr12:51125805 | C | T | 331 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(328): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.123-7033G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51125805 | |||||||
| chr12:51125835 | T | C | 10 | a0001c0001t0001g0145 a0001c0001t0001g0164 a0001c0001t0001g0212 others(7): Show |
10 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.123-7063A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51125835 | |||||||
| chr12:51125835 | T | G | 11 | a0001c0001t0003g0021 a0001c0001t0003g0023 a0001c0001t0003g0024 others(8): Show |
11 | HG02027.hp1 HG02155.hp2 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.123-7063A>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51125835 | |||||||
| chr12:51125867 | A | G | 258 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(255): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.123-7095T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51125867 | |||||||
| chr12:51125997 | G | A | 50 | a0001c0001t0003g0002 a0001c0001t0003g0013 a0001c0001t0003g0014 others(47): Show |
51 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.123-7225C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51125997 | |||||||
| chr12:51126001 | C | G | 5 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 others(2): Show |
5 | HG02717.hp2 HG03041.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.123-7229G>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51126001 | |||||||
| chr12:51126027 | G | A | 3 | a0001c0001t0006g0200 a0001c0001t0006g0201 a0001c0001t0006g0202 |
3 | HG02976.hp1 HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.123-7255C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51126027 | |||||||
| chr12:51126056 | C | T | 4 | a0001c0001t0002g0298 a0001c0001t0002g0299 a0001c0001t0002g0300 others(1): Show |
4 | HG02109.hp1 HG03471.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-7284G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51126056 | |||||||
| chr12:51126059 | T | G | 49 | a0001c0001t0003g0002 a0001c0001t0003g0013 a0001c0001t0003g0014 others(46): Show |
50 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.123-7287A>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51126059 | |||||||
| chr12:51126100 | T | G | 3 | a0001c0001t0003g0032 a0001c0001t0003g0033 a0001c0001t0003g0049 |
3 | HG02572.hp2 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.123-7328A>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51126100 | |||||||
| chr12:51126232 | C | CA | 207 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(204): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.123-7461dupT | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51126232 | |||||||
| chr12:51126232 | C | CAA | 7 | a0001c0001t0001g0226 a0001c0001t0001g0235 a0001c0001t0001g0305 others(4): Show |
7 | HG00544.hp1 HG02258.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.123-7462_123-7461d others(4): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51126232 | |||||||
| chr12:51126454 | C | T | 1 | a0001c0001t0001g0266 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.123-7682G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51126454 | |||||||
| chr12:51126723 | T | G | 11 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0121 others(8): Show |
11 | HG01346.hp2 HG02145.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.123-7951A>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51126723 | |||||||
| chr12:51126802 | G | A | 1 | a0001c0001t0003g0016 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.123-8030C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51126802 | |||||||
| chr12:51126874 | G | T | 328 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(325): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.123-8102C>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51126874 | |||||||
| chr12:51126936 | G | A | 13 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(10): Show |
13 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.123-8164C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51126936 | |||||||
| chr12:51127038 | T | C | 1 | a0001c0001t0002g0300 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.123-8266A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51127038 | |||||||
| chr12:51127093 | G | T | 5 | a0001c0001t0004g0074 a0001c0001t0004g0092 a0001c0001t0004g0095 others(2): Show |
5 | HG00735.hp2 HG01934.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.123-8321C>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51127093 | |||||||
| chr12:51127746 | G | A | 1 | a0001c0001t0001g0149 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.123-8974C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51127746 | |||||||
| chr12:51127765 | T | A | 2 | a0001c0001t0001g0211 a0001c0001t0001g0308 |
2 | HG01361.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.123-8993A>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51127765 | |||||||
| chr12:51127818 | C | A | 1 | a0001c0001t0001g0218 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.123-9046G>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51127818 | |||||||
| chr12:51127843 | A | T | 273 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(270): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.123-9071T>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51127843 | |||||||
| chr12:51127925 | C | CT | 244 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(241): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.123-9154dupA | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51127925 | |||||||
| chr12:51127925 | C | CTT | 29 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 others(26): Show |
29 | HG01346.hp2 HG02109.hp1 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.123-9155_123-9154d others(4): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51127925 | |||||||
| chr12:51127983 | G | A | 1 | a0001c0001t0012g0161 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.123-9211C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51127983 | |||||||
| chr12:51127997 | G | A | 1 | a0001c0001t0007g0333 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.123-9225C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51127997 | |||||||
| chr12:51128044 | T | A | 1 | a0001c0001t0001g0326 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.123-9272A>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51128044 | |||||||
| chr12:51128082 | G | A | 1 | a0001c0001t0001g0217 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.123-9310C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51128082 | |||||||
| chr12:51128139 | G | A | 60 | a0001c0001t0003g0002 a0001c0001t0003g0010 a0001c0001t0003g0011 others(57): Show |
61 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.123-9367C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51128139 | |||||||
| chr12:51128286 | G | A | 1 | a0001c0001t0016g0302 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.123-9514C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51128286 | |||||||
| chr12:51128299 | A | T | 11 | a0001c0001t0001g0145 a0001c0001t0001g0164 a0001c0001t0001g0212 others(8): Show |
11 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.123-9527T>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51128299 | |||||||
| chr12:51128478 | TA | T | 242 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(239): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.123-9707delT | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51128478 | |||||||
| chr12:51128478 | TAA | T | 6 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 others(3): Show |
6 | HG02717.hp2 HG03041.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.123-9708_123-9707d others(4): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51128478 | |||||||
| chr12:51128482 | A | T | 1 | a0001c0001t0002g0156 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.123-9710T>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51128482 | |||||||
| chr12:51128484 | A | C | 1 | a0001c0001t0004g0080 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.123-9712T>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51128484 | |||||||
| chr12:51128492 | A | C | 11 | a0001c0001t0001g0145 a0001c0001t0001g0164 a0001c0001t0001g0212 others(8): Show |
11 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.123-9720T>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51128492 | |||||||
| chr12:51128492 | AC | A | 4 | a0001c0001t0002g0298 a0001c0001t0002g0299 a0001c0001t0002g0300 others(1): Show |
4 | HG02109.hp1 HG03471.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-9721delG | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51128492 | |||||||
| chr12:51128493 | C | A | 70 | a0001c0001t0001g0145 a0001c0001t0001g0164 a0001c0001t0001g0212 others(67): Show |
71 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.123-9721G>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51128493 | |||||||
| chr12:51128498 | A | AC | 3 | a0001c0001t0003g0032 a0001c0001t0003g0038 a0001c0001t0003g0054 |
3 | HG01106.hp2 HG01192.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.123-9727_123-9726i others(3): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51128498 | |||||||
| chr12:51128498 | A | C | 51 | a0001c0001t0003g0002 a0001c0001t0003g0010 a0001c0001t0003g0011 others(48): Show |
52 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.123-9726T>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51128498 | |||||||
| chr12:51128502 | C | A | 4 | a0001c0001t0002g0197 a0001c0001t0002g0290 a0001c0001t0002g0301 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-9730G>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51128502 | |||||||
| chr12:51128782 | T | G | 2 | a0001c0001t0001g0305 a0001c0001t0001g0306 |
2 | HG02258.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.123-10010A>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51128782 | |||||||
| chr12:51128836 | G | A | 2 | a0001c0001t0016g0302 a0001c0001t0027g0244 |
2 | HG01884.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.123-10064C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51128836 | |||||||
| chr12:51128867 | T | C | 1 | a0001c0001t0021g0252 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.123-10095A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51128867 | |||||||
| chr12:51129050 | T | TA | 5 | a0001c0001t0004g0074 a0001c0001t0004g0092 a0001c0001t0004g0095 others(2): Show |
5 | HG00735.hp2 HG01934.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.123-10279dupT | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51129050 | |||||||
| chr12:51129131 | C | T | 1 | a0001c0001t0005g0126 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.123-10359G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51129131 | |||||||
| chr12:51129321 | G | A | 1 | a0001c0001t0018g0335 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.123-10549C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51129321 | |||||||
| chr12:51129489 | C | G | 54 | a0001c0001t0004g0003 a0001c0001t0004g0004 a0001c0001t0004g0005 others(51): Show |
57 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.123-10717G>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51129489 | |||||||
| chr12:51129514 | C | CA | 17 | a0001c0001t0003g0039 a0001c0001t0004g0005 a0001c0001t0004g0106 others(14): Show |
18 | HG00544.hp2 HG02523.hp1 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.123-10743dupT | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51129514 | |||||||
| chr12:51129514 | CAAAAAA | C | 210 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(207): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.123-10748_123-1074 others(10): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51129514 | |||||||
| chr12:51129630 | C | G | 1 | a0001c0001t0002g0191 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.123-10858G>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51129630 | |||||||
| chr12:51129836 | G | GA | 263 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(260): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.123-11065_123-1106 others(5): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51129836 | |||||||
| chr12:51129837 | G | A | 325 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(322): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.123-11065C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51129837 | |||||||
| chr12:51129837 | G | GA | 6 | a0001c0001t0002g0156 a0001c0001t0013g0006 a0001c0001t0013g0155 others(3): Show |
7 | HG00140.hp1 HG01109.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.123-11066dupT | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51129837 | |||||||
| chr12:51129903 | A | G | 1 | a0001c0001t0001g0260 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.123-11131T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51129903 | |||||||
| chr12:51129984 | CA | C | 272 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(269): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.123-11213delT | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51129984 | |||||||
| chr12:51130140 | T | A | 272 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(269): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.123-11368A>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51130140 | |||||||
| chr12:51130150 | C | A | 272 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(269): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.123-11378G>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51130150 | |||||||
| chr12:51130209 | C | A | 2 | a0001c0001t0013g0155 a0001c0001t0013g0297 |
2 | HG02723.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.123-11437G>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51130209 | |||||||
| chr12:51130242 | T | C | 273 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(270): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.123-11470A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51130242 | |||||||
| chr12:51130300 | C | T | 2 | a0001c0001t0018g0009 a0001c0001t0018g0335 |
3 | HG01069.hp1 HG01071.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.123-11528G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51130300 | |||||||
| chr12:51130451 | G | A | 1 | a0001c0001t0004g0097 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.123-11679C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51130451 | |||||||
| chr12:51130471 | C | CA | 60 | a0001c0001t0003g0002 a0001c0001t0003g0010 a0001c0001t0003g0011 others(57): Show |
61 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.123-11700dupT | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51130471 | |||||||
| chr12:51130512 | C | T | 1 | a0001c0001t0001g0326 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.123-11740G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51130512 | |||||||
| chr12:51130676 | A | T | 56 | a0001c0001t0003g0002 a0001c0001t0003g0010 a0001c0001t0003g0011 others(53): Show |
57 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.123-11904T>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51130676 | |||||||
| chr12:51130698 | A | T | 3 | a0001c0001t0016g0204 a0001c0001t0016g0206 a0001c0001t0031g0146 |
3 | HG04228.hp2 NA18747.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.123-11926T>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51130698 | |||||||
| chr12:51130725 | G | A | 1 | a0001c0001t0002g0237 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.123-11953C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51130725 | |||||||
| chr12:51130941 | T | C | 1 | a0001c0001t0001g0151 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.123-12169A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51130941 | |||||||
| chr12:51130945 | G | A | 60 | a0001c0001t0003g0002 a0001c0001t0003g0010 a0001c0001t0003g0011 others(57): Show |
61 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.123-12173C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51130945 | |||||||
| chr12:51130987 | CA | C | 9 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 others(6): Show |
9 | HG02109.hp1 HG02717.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.123-12216delT | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51130987 | |||||||
| chr12:51131052 | G | A | 4 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(1): Show |
4 | HG02451.hp2 HG02886.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-12280C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51131052 | |||||||
| chr12:51131058 | G | A | 4 | a0001c0001t0002g0298 a0001c0001t0002g0299 a0001c0001t0002g0300 others(1): Show |
4 | HG02109.hp1 HG03471.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-12286C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51131058 | |||||||
| chr12:51131067 | C | T | 58 | a0001c0001t0004g0003 a0001c0001t0004g0004 a0001c0001t0004g0005 others(55): Show |
62 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.123-12295G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51131067 | |||||||
| chr12:51131165 | T | TA | 25 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(22): Show |
26 | HG01069.hp1 HG01071.hp2 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.123-12394dupT | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51131165 | |||||||
| chr12:51131172 | A | G | 4 | a0001c0001t0002g0298 a0001c0001t0002g0299 a0001c0001t0002g0300 others(1): Show |
4 | HG02109.hp1 HG03471.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-12400T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51131172 | |||||||
| chr12:51131208 | G | A | 1 | a0001c0001t0002g0237 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.123-12436C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51131208 | |||||||
| chr12:51131259 | C | T | 1 | a0001c0001t0005g0123 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.123-12487G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51131259 | |||||||
| chr12:51131332 | C | CA | 172 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(169): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.123-12561dupT | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51131332 | |||||||
| chr12:51131332 | C | CAA | 7 | a0001c0001t0001g0216 a0001c0001t0001g0240 a0001c0001t0001g0257 others(4): Show |
7 | HG00735.hp1 HG02145.hp2 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.123-12562_123-1256 others(6): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51131332 | |||||||
| chr12:51131408 | A | C | 1 | a0001c0001t0027g0244 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.123-12636T>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51131408 | |||||||
| chr12:51131626 | C | G | 1 | a0001c0001t0024g0066 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.123-12854G>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51131626 | |||||||
| chr12:51131638 | T | C | 11 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0121 others(8): Show |
11 | HG01346.hp2 HG02145.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.123-12866A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51131638 | |||||||
| chr12:51132163 | T | C | 273 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(270): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.123-13391A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51132163 | |||||||
| chr12:51132243 | G | A | 2 | a0001c0001t0001g0223 a0001c0001t0026g0186 |
2 | HG00280.hp1 HG00642.hp1 |
intron_variant | MODIFIER | c.123-13471C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51132243 | |||||||
| chr12:51132298 | CTTTAACA others(66): Show |
C | 2 | a0001c0001t0001g0293 a0001c0001t0001g0296 |
2 | HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.123-13599_123-1352 others(77): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51132298 | |||||||
| chr12:51132357 | C | CTT | 22 | a0001c0001t0004g0005 a0001c0001t0004g0075 a0001c0001t0004g0077 others(19): Show |
22 | HG00544.hp2 HG00597.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.123-13587_123-1358 others(6): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51132357 | |||||||
| chr12:51132357 | C | CTTT | 28 | a0001c0001t0004g0003 a0001c0001t0004g0004 a0001c0001t0004g0005 others(25): Show |
29 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(26): Show |
intron_variant | MODIFIER | c.123-13588_123-1358 others(7): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51132357 | |||||||
| chr12:51132357 | C | CTTTTTT | 7 | a0001c0001t0001g0275 a0001c0001t0001g0294 a0001c0001t0001g0318 others(4): Show |
7 | HG03041.hp2 HG03471.hp2 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.123-13591_123-1358 others(10): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51132357 | |||||||
| chr12:51132357 | C | CTTTTTTT | 30 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0218 others(27): Show |
31 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.123-13592_123-1358 others(11): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51132357 | |||||||
| chr12:51132357 | C | CTTTTTTT others(1): Show |
55 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(52): Show |
55 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(52): Show |
intron_variant | MODIFIER | c.123-13593_123-1358 others(12): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51132357 | |||||||
| chr12:51132357 | C | CTTTTTTT others(2): Show |
45 | a0001c0001t0001g0008 a0001c0001t0001g0140 a0001c0001t0001g0152 others(42): Show |
46 | HG00639.hp2 HG00733.hp2 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.123-13594_123-1358 others(13): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51132357 | |||||||
| chr12:51132357 | C | CTTTTTTT others(3): Show |
25 | a0001c0001t0001g0139 a0001c0001t0001g0215 a0001c0001t0001g0216 others(22): Show |
25 | HG00735.hp1 HG00741.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.123-13595_123-1358 others(14): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51132357 | |||||||
| chr12:51132357 | C | CTTTTTTT others(4): Show |
7 | a0001c0001t0001g0212 a0001c0001t0001g0234 a0001c0001t0002g0254 others(4): Show |
7 | HG01069.hp2 HG02647.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.123-13596_123-1358 others(15): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51132357 | |||||||
| chr12:51132357 | C | CTTTTTTT others(5): Show |
7 | a0001c0001t0001g0145 a0001c0001t0001g0151 a0001c0001t0001g0164 others(4): Show |
7 | HG01346.hp2 HG01891.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.123-13597_123-1358 others(16): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51132357 | |||||||
| chr12:51132357 | C | CTTTTTTT others(6): Show |
2 | a0001c0001t0001g0306 a0001c0001t0002g0329 |
2 | HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.123-13598_123-1358 others(17): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51132357 | |||||||
| chr12:51132357 | C | CTTTTTTT others(7): Show |
1 | a0001c0001t0005g0128 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.123-13599_123-1358 others(18): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51132357 | |||||||
| chr12:51132357 | C | CTTTTTTT others(8): Show |
2 | a0001c0001t0005g0131 a0001c0001t0005g0134 |
2 | HG02145.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.123-13600_123-1358 others(19): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51132357 | |||||||
| chr12:51132357 | C | CTTTTTTT others(9): Show |
1 | a0001c0001t0005g0130 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.123-13601_123-1358 others(20): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51132357 | |||||||
| chr12:51132357 | C | CTTTTTTT others(13): Show |
1 | a0001c0001t0005g0127 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.123-13605_123-1358 others(24): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51132357 | |||||||
| chr12:51132357 | C | CTTTTTTT others(16): Show |
1 | a0001c0001t0017g0303 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.123-13608_123-1358 others(27): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51132357 | |||||||
| chr12:51132357 | CTT | C | 16 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0014 others(13): Show |
16 | HG00597.hp1 HG01081.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.123-13587_123-1358 others(6): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51132357 | |||||||
| chr12:51132357 | CTTT | C | 44 | a0001c0001t0003g0002 a0001c0001t0003g0013 a0001c0001t0003g0015 others(41): Show |
45 | HG00280.hp2 HG00408.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.123-13588_123-1358 others(7): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51132357 | |||||||
| chr12:51132357 | CTTTTTTT others(1): Show |
C | 6 | a0001c0001t0002g0188 a0001c0001t0013g0006 a0001c0001t0013g0155 others(3): Show |
7 | HG00140.hp1 HG02698.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.123-13593_123-1358 others(12): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51132357 | |||||||
| chr12:51132357 | CTTTTTTT others(2): Show |
C | 13 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(10): Show |
13 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.123-13594_123-1358 others(13): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51132357 | |||||||
| chr12:51132357 | CTTTTTTT others(3): Show |
C | 3 | a0001c0001t0001g0230 a0001c0001t0001g0262 a0001c0001t0002g0190 |
3 | HG00639.hp1 NA19085.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.123-13595_123-1358 others(14): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51132357 | |||||||
| chr12:51132357 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0220 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.123-13596_123-1358 others(15): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51132357 | |||||||
| chr12:51132357 | CTTTTTTT others(7): Show |
C | 2 | a0001c0001t0018g0009 a0001c0001t0018g0335 |
3 | HG01069.hp1 HG01071.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.123-13599_123-1358 others(18): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51132357 | |||||||
| chr12:51132357 | CTTTTTTT others(8): Show |
C | 2 | a0001c0001t0024g0066 a0001c0001t0032g0334 |
2 | HG02630.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.123-13600_123-1358 others(19): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51132357 | |||||||
| chr12:51132400 | G | A | 1 | a0001c0001t0003g0065 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.123-13628C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51132400 | |||||||
| chr12:51132954 | G | A | 33 | a0001c0001t0001g0145 a0001c0001t0001g0164 a0001c0001t0001g0212 others(30): Show |
33 | HG01346.hp2 HG01884.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.123-14182C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51132954 | |||||||
| chr12:51133144 | G | A | 328 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(325): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.123-14372C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51133144 | |||||||
| chr12:51133297 | T | C | 3 | a0001c0001t0016g0204 a0001c0001t0016g0206 a0001c0001t0031g0146 |
3 | HG04228.hp2 NA18747.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.123-14525A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51133297 | |||||||
| chr12:51133330 | C | T | 60 | a0001c0001t0003g0002 a0001c0001t0003g0010 a0001c0001t0003g0011 others(57): Show |
61 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.123-14558G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51133330 | |||||||
| chr12:51133558 | G | A | 5 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 others(2): Show |
5 | HG02717.hp2 HG03041.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.123-14786C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51133558 | |||||||
| chr12:51133730 | C | A | 1 | a0001c0001t0001g0231 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.123-14958G>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51133730 | |||||||
| chr12:51133921 | C | CA | 54 | a0001c0001t0004g0003 a0001c0001t0004g0004 a0001c0001t0004g0005 others(51): Show |
58 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.123-15150dupT | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51133921 | |||||||
| chr12:51133921 | CA | C | 229 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(226): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.123-15150delT | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51133921 | |||||||
| chr12:51133940 | G | A | 1 | a0001c0001t0005g0133 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.123-15168C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51133940 | |||||||
| chr12:51134174 | G | A | 1 | a0001c0001t0003g0056 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.123-15402C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51134174 | |||||||
| chr12:51134253 | C | G | 20 | a0001c0001t0005g0118 a0001c0001t0005g0119 a0001c0001t0005g0120 others(17): Show |
20 | HG01346.hp2 HG02145.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.123-15481G>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51134253 | |||||||
| chr12:51134321 | A | G | 1 | a0001c0001t0017g0303 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.123-15549T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51134321 | |||||||
| chr12:51134448 | C | T | 1 | a0001c0001t0017g0303 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.123-15676G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51134448 | |||||||
| chr12:51134622 | C | G | 1 | a0001c0001t0001g0223 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.123-15850G>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51134622 | |||||||
| chr12:51134662 | T | A | 3 | a0001c0001t0016g0204 a0001c0001t0016g0206 a0001c0001t0031g0146 |
3 | HG04228.hp2 NA18747.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.123-15890A>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51134662 | |||||||
| chr12:51134793 | T | G | 1 | a0001c0001t0022g0336 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.123-16021A>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51134793 | |||||||
| chr12:51134845 | CA | C | 3 | a0001c0001t0016g0204 a0001c0001t0016g0206 a0001c0001t0031g0146 |
3 | HG04228.hp2 NA18747.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.123-16074delT | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51134845 | |||||||
| chr12:51134934 | C | A | 1 | a0001c0001t0003g0049 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.123-16162G>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51134934 | |||||||
| chr12:51134977 | G | T | 1 | a0001c0001t0008g0117 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.123-16205C>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51134977 | |||||||
| chr12:51135071 | C | T | 12 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 others(9): Show |
12 | HG02109.hp1 HG02717.hp2 HG03041.hp2 others(9): Show |
intron_variant | MODIFIER | c.123-16299G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51135071 | |||||||
| chr12:51135113 | GA | G | 263 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(260): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.123-16342delT | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51135113 | |||||||
| chr12:51135113 | GAA | G | 6 | a0001c0001t0002g0298 a0001c0001t0002g0299 a0001c0001t0002g0300 others(3): Show |
6 | HG02109.hp1 HG03471.hp2 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.123-16343_123-1634 others(6): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51135113 | |||||||
| chr12:51135122 | A | C | 2 | a0001c0001t0001g0229 a0001c0001t0001g0235 |
2 | NA18994.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.123-16350T>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51135122 | |||||||
| chr12:51135353 | G | A | 6 | a0001c0001t0002g0156 a0001c0001t0013g0006 a0001c0001t0013g0155 others(3): Show |
7 | HG00140.hp1 HG01109.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.123-16581C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51135353 | |||||||
| chr12:51135434 | C | CA | 4 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0296 others(1): Show |
4 | HG02717.hp2 HG03041.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.123-16663dupT | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51135434 | |||||||
| chr12:51135436 | C | A | 5 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 others(2): Show |
5 | HG02717.hp2 HG03041.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.123-16664G>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51135436 | |||||||
| chr12:51135436 | C | CA | 250 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(247): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.123-16665dupT | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51135436 | |||||||
| chr12:51135437 | A | AC | 12 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(9): Show |
13 | HG00140.hp1 HG01109.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.123-16666_123-1666 others(5): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51135437 | |||||||
| chr12:51135440 | A | AG | 3 | a0001c0001t0016g0204 a0001c0001t0016g0206 a0001c0001t0031g0146 |
3 | HG04228.hp2 NA18747.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.123-16669_123-1666 others(5): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51135440 | |||||||
| chr12:51135448 | C | G | 56 | a0001c0001t0003g0002 a0001c0001t0003g0010 a0001c0001t0003g0011 others(53): Show |
57 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.123-16676G>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51135448 | |||||||
| chr12:51135622 | G | A | 7 | a0001c0001t0001g0145 a0001c0001t0001g0164 a0001c0001t0001g0212 others(4): Show |
7 | HG01891.hp1 HG02055.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.123-16850C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51135622 | |||||||
| chr12:51135707 | A | G | 42 | a0001c0001t0001g0145 a0001c0001t0001g0164 a0001c0001t0001g0212 others(39): Show |
42 | HG01346.hp2 HG01884.hp2 HG01891.hp1 others(39): Show |
intron_variant | MODIFIER | c.123-16935T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51135707 | |||||||
| chr12:51135840 | C | T | 1 | a0001c0001t0001g0305 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.123-17068G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51135840 | |||||||
| chr12:51136008 | G | A | 1 | a0001c0001t0001g0267 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.123-17236C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51136008 | |||||||
| chr12:51136018 | G | T | 5 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 others(2): Show |
5 | HG02717.hp2 HG03041.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.123-17246C>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51136018 | |||||||
| chr12:51136148 | T | C | 1 | a0001c0001t0001g0250 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.123-17376A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51136148 | |||||||
| chr12:51136226 | T | C | 1 | a0001c0001t0001g0248 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.123-17454A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51136226 | |||||||
| chr12:51136285 | C | A | 1 | a0001c0001t0002g0173 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.123-17513G>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51136285 | |||||||
| chr12:51136302 | TA | T | 268 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(265): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.123-17531delT | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51136302 | |||||||
| chr12:51136311 | A | G | 1 | a0001c0001t0001g0325 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.123-17539T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51136311 | |||||||
| chr12:51136330 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.123-17558C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51136330 | |||||||
| chr12:51136440 | C | A | 1 | a0001c0001t0002g0281 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.123-17668G>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51136440 | |||||||
| chr12:51136465 | G | A | 43 | a0001c0001t0001g0145 a0001c0001t0001g0164 a0001c0001t0001g0212 others(40): Show |
43 | HG01346.hp2 HG01884.hp2 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.123-17693C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51136465 | |||||||
| chr12:51136633 | A | G | 6 | a0001c0001t0002g0298 a0001c0001t0002g0299 a0001c0001t0002g0300 others(3): Show |
6 | HG02109.hp1 HG03471.hp2 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.123-17861T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51136633 | |||||||
| chr12:51136649 | A | AC | 331 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(328): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.123-17878dupG | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51136649 | |||||||
| chr12:51136664 | T | A | 272 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(269): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.123-17892A>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51136664 | |||||||
| chr12:51136734 | G | A | 20 | a0001c0001t0005g0118 a0001c0001t0005g0119 a0001c0001t0005g0120 others(17): Show |
20 | HG01346.hp2 HG02145.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.123-17962C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51136734 | |||||||
| chr12:51136889 | G | A | 1 | a0001c0001t0002g0173 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.123-18117C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51136889 | |||||||
| chr12:51137003 | G | T | 2 | a0001c0001t0016g0206 a0001c0001t0031g0146 |
2 | NA18747.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.123-18231C>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51137003 | |||||||
| chr12:51137013 | T | C | 56 | a0001c0001t0003g0002 a0001c0001t0003g0010 a0001c0001t0003g0011 others(53): Show |
57 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.123-18241A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51137013 | |||||||
| chr12:51137157 | A | T | 1 | a0001c0001t0025g0086 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.123-18385T>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51137157 | |||||||
| chr12:51137179 | T | C | 20 | a0001c0001t0005g0118 a0001c0001t0005g0119 a0001c0001t0005g0120 others(17): Show |
20 | HG01346.hp2 HG02145.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.123-18407A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51137179 | |||||||
| chr12:51137243 | C | G | 2 | a0001c0001t0002g0205 a0001c0001t0002g0239 |
2 | NA18947.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.123-18471G>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51137243 | |||||||
| chr12:51137326 | T | A | 1 | a0001c0001t0001g0278 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.123-18554A>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51137326 | |||||||
| chr12:51137328 | T | A | 57 | a0001c0001t0003g0002 a0001c0001t0003g0010 a0001c0001t0003g0011 others(54): Show |
58 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.123-18556A>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51137328 | |||||||
| chr12:51137724 | A | G | 11 | a0001c0001t0001g0145 a0001c0001t0001g0164 a0001c0001t0001g0212 others(8): Show |
11 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.123-18952T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51137724 | |||||||
| chr12:51137740 | T | C | 59 | a0001c0001t0004g0003 a0001c0001t0004g0004 a0001c0001t0004g0005 others(56): Show |
63 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.123-18968A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51137740 | |||||||
| chr12:51137793 | A | G | 146 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(143): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.123-19021T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51137793 | |||||||
| chr12:51137895 | C | T | 1 | a0001c0001t0016g0302 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.123-19123G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51137895 | |||||||
| chr12:51137931 | T | C | 330 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(327): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.123-19159A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51137931 | |||||||
| chr12:51138254 | G | A | 1 | a0001c0001t0007g0331 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.123-19482C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51138254 | |||||||
| chr12:51138267 | G | T | 4 | a0001c0001t0002g0298 a0001c0001t0002g0299 a0001c0001t0002g0300 others(1): Show |
4 | HG02109.hp1 HG03471.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-19495C>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51138267 | |||||||
| chr12:51138286 | C | T | 57 | a0001c0001t0003g0002 a0001c0001t0003g0010 a0001c0001t0003g0011 others(54): Show |
58 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.123-19514G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51138286 | |||||||
| chr12:51138446 | T | C | 3 | a0001c0001t0016g0204 a0001c0001t0017g0199 a0001c0001t0017g0203 |
3 | HG00140.hp1 HG02698.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.123-19674A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51138446 | |||||||
| chr12:51138491 | G | T | 4 | a0001c0001t0002g0298 a0001c0001t0002g0299 a0001c0001t0002g0300 others(1): Show |
4 | HG02109.hp1 HG03471.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-19719C>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51138491 | |||||||
| chr12:51138653 | T | A | 2 | a0001c0001t0004g0082 a0001c0001t0004g0113 |
2 | HG00642.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.123-19881A>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51138653 | |||||||
| chr12:51138742 | G | A | 57 | a0001c0001t0003g0002 a0001c0001t0003g0010 a0001c0001t0003g0011 others(54): Show |
58 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.123-19970C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51138742 | |||||||
| chr12:51138788 | G | A | 59 | a0001c0001t0004g0003 a0001c0001t0004g0004 a0001c0001t0004g0005 others(56): Show |
63 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.123-20016C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51138788 | |||||||
| chr12:51138826 | C | A | 9 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 others(6): Show |
9 | HG02109.hp1 HG02717.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.123-20054G>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51138826 | |||||||
| chr12:51138826 | C | T | 3 | a0001c0001t0002g0197 a0001c0001t0002g0290 a0001c0001t0002g0301 |
3 | HG01167.hp1 HG01169.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.123-20054G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51138826 | |||||||
| chr12:51138903 | G | A | 2 | a0001c0001t0002g0170 a0001c0001t0002g0171 |
2 | HG02683.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.123-20131C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51138903 | |||||||
| chr12:51138928 | A | G | 331 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(328): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.123-20156T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51138928 | |||||||
| chr12:51138957 | G | C | 29 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 others(26): Show |
29 | HG01346.hp2 HG02109.hp1 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.123-20185C>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51138957 | |||||||
| chr12:51139033 | C | T | 3 | a0001c0001t0014g0018 a0001c0001t0014g0019 a0001c0001t0014g0020 |
3 | NA19001.hp1 NA19009.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.123-20261G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51139033 | |||||||
| chr12:51139075 | A | G | 12 | a0001c0001t0004g0077 a0001c0001t0004g0082 a0001c0001t0004g0084 others(9): Show |
12 | HG00423.hp2 HG00642.hp2 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.123-20303T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51139075 | |||||||
| chr12:51139393 | C | T | 40 | a0001c0001t0001g0145 a0001c0001t0001g0164 a0001c0001t0001g0212 others(37): Show |
40 | HG01346.hp2 HG01884.hp2 HG01891.hp1 others(37): Show |
intron_variant | MODIFIER | c.123-20621G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51139393 | |||||||
| chr12:51139482 | C | T | 5 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 others(2): Show |
5 | HG02717.hp2 HG03041.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.123-20710G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51139482 | |||||||
| chr12:51139505 | G | T | 5 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 others(2): Show |
5 | HG02717.hp2 HG03041.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.123-20733C>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51139505 | |||||||
| chr12:51139552 | ATT | A | 3 | a0001c0001t0006g0200 a0001c0001t0006g0201 a0001c0001t0006g0202 |
3 | HG02976.hp1 HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.123-20782_123-2078 others(6): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51139552 | |||||||
| chr12:51139763 | CCTCAA | C | 210 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(207): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.123-20996_123-2099 others(9): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51139763 | |||||||
| chr12:51139774 | T | C | 57 | a0001c0001t0003g0002 a0001c0001t0003g0010 a0001c0001t0003g0011 others(54): Show |
58 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.123-21002A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51139774 | |||||||
| chr12:51139984 | T | C | 5 | a0001c0001t0001g0145 a0001c0001t0001g0164 a0001c0001t0001g0212 others(2): Show |
5 | HG01891.hp1 HG02055.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.123-21212A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51139984 | |||||||
| chr12:51140443 | T | C | 2 | a0001c0001t0006g0314 a0001c0001t0006g0316 |
2 | HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.123-21671A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51140443 | |||||||
| chr12:51140444 | T | C | 1 | a0001c0001t0006g0323 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.123-21672A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51140444 | |||||||
| chr12:51140445 | C | CT | 120 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(117): Show |
125 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.123-21674dupA | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51140445 | |||||||
| chr12:51140445 | C | T | 3 | a0001c0001t0006g0314 a0001c0001t0006g0316 a0001c0001t0006g0323 |
3 | HG02145.hp2 HG02965.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.123-21673G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51140445 | |||||||
| chr12:51140445 | CT | C | 53 | a0001c0001t0003g0060 a0001c0001t0004g0003 a0001c0001t0004g0004 others(50): Show |
56 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.123-21674delA | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51140445 | |||||||
| chr12:51140449 | T | C | 8 | a0001c0001t0005g0123 a0001c0001t0005g0125 a0001c0001t0005g0126 others(5): Show |
8 | HG02698.hp1 HG02717.hp1 HG03239.hp1 others(5): Show |
intron_variant | MODIFIER | c.123-21677A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51140449 | |||||||
| chr12:51140451 | T | C | 2 | a0001c0001t0004g0105 a0001c0001t0004g0106 |
2 | NA18961.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.123-21679A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51140451 | |||||||
| chr12:51140870 | G | A | 9 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 others(6): Show |
9 | HG02109.hp1 HG02717.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.123-22098C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51140870 | |||||||
| chr12:51140871 | C | T | 9 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 others(6): Show |
9 | HG02109.hp1 HG02717.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.123-22099G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51140871 | |||||||
| chr12:51140929 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.123-22157C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51140929 | |||||||
| chr12:51140980 | G | A | 170 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(167): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.123-22208C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51140980 | |||||||
| chr12:51141072 | A | T | 1 | a0001c0001t0001g0295 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.123-22300T>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51141072 | |||||||
| chr12:51141103 | A | AT | 100 | a0001c0001t0001g0145 a0001c0001t0001g0164 a0001c0001t0001g0212 others(97): Show |
101 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.123-22332dupA | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51141103 | |||||||
| chr12:51141103 | A | ATT | 172 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(169): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.123-22333_123-2233 others(6): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51141103 | |||||||
| chr12:51141124 | G | T | 1 | a0001c0001t0001g0145 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.123-22352C>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51141124 | |||||||
| chr12:51141149 | C | T | 2 | a0001c0001t0024g0066 a0001c0001t0032g0334 |
2 | HG02630.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.123-22377G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51141149 | |||||||
| chr12:51141228 | G | C | 1 | a0001c0001t0004g0077 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.123-22456C>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51141228 | |||||||
| chr12:51141235 | G | A | 1 | a0001c0001t0016g0302 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.123-22463C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51141235 | |||||||
| chr12:51141558 | AC | A | 3 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 |
3 | NA18983.hp2 NA19002.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.123-22787delG | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51141558 | |||||||
| chr12:51141660 | G | T | 1 | a0001c0001t0002g0187 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.123-22888C>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51141660 | |||||||
| chr12:51141687 | G | A | 56 | a0001c0001t0003g0002 a0001c0001t0003g0010 a0001c0001t0003g0011 others(53): Show |
57 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.123-22915C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51141687 | |||||||
| chr12:51141726 | C | G | 1 | a0001c0001t0003g0017 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.123-22954G>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51141726 | |||||||
| chr12:51141745 | C | CA | 8 | a0001c0001t0001g0140 a0001c0001t0001g0229 a0001c0001t0001g0293 others(5): Show |
8 | HG02717.hp2 HG03041.hp2 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.123-22974dupT | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51141745 | |||||||
| chr12:51141778 | C | T | 1 | a0001c0001t0001g0306 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.123-23006G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51141778 | |||||||
| chr12:51141859 | T | G | 1 | a0001c0001t0002g0192 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.123-23087A>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51141859 | |||||||
| chr12:51141905 | C | CA | 69 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0211 others(66): Show |
70 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.123-23134dupT | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51141905 | |||||||
| chr12:51141905 | C | CAA | 12 | a0001c0001t0003g0026 a0001c0001t0003g0048 a0001c0001t0003g0054 others(9): Show |
12 | HG00280.hp2 HG01192.hp2 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.123-23135_123-2313 others(6): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51141905 | |||||||
| chr12:51141925 | C | A | 1 | a0001c0001t0005g0118 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.123-23153G>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51141925 | |||||||
| chr12:51141970 | C | T | 4 | a0001c0001t0012g0158 a0001c0001t0012g0159 a0001c0001t0012g0160 others(1): Show |
4 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-23198G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51141970 | |||||||
| chr12:51142066 | G | A | 32 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0150 others(29): Show |
35 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.123-23294C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51142066 | |||||||
| chr12:51142127 | C | T | 215 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(212): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.123-23355G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51142127 | |||||||
| chr12:51142203 | C | CA | 37 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 others(34): Show |
37 | HG00609.hp1 HG01346.hp1 HG01884.hp1 others(34): Show |
intron_variant | MODIFIER | c.123-23432dupT | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51142203 | |||||||
| chr12:51142203 | C | CAA | 121 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0147 others(118): Show |
126 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.123-23433_123-2343 others(6): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51142203 | |||||||
| chr12:51142203 | C | CAAA | 47 | a0001c0001t0001g0140 a0001c0001t0001g0149 a0001c0001t0001g0151 others(44): Show |
47 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.123-23434_123-2343 others(7): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51142203 | |||||||
| chr12:51142203 | C | CAAAA | 19 | a0001c0001t0001g0145 a0001c0001t0001g0164 a0001c0001t0001g0212 others(16): Show |
19 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.123-23435_123-2343 others(8): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51142203 | |||||||
| chr12:51142203 | CA | C | 55 | a0001c0001t0003g0010 a0001c0001t0003g0013 a0001c0001t0003g0014 others(52): Show |
58 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.123-23432delT | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51142203 | |||||||
| chr12:51142203 | CAAAAAAA others(6): Show |
C | 4 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(1): Show |
4 | HG02451.hp2 HG02886.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-23444_123-2343 others(17): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51142203 | |||||||
| chr12:51142260 | A | G | 57 | a0001c0001t0003g0002 a0001c0001t0003g0010 a0001c0001t0003g0011 others(54): Show |
58 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.123-23488T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51142260 | |||||||
| chr12:51142501 | T | C | 6 | a0001c0001t0001g0317 a0001c0001t0001g0318 a0001c0001t0001g0319 others(3): Show |
6 | HG01884.hp2 HG02723.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.123-23729A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51142501 | |||||||
| chr12:51142742 | C | G | 36 | a0001c0001t0001g0145 a0001c0001t0001g0212 a0001c0001t0001g0292 others(33): Show |
36 | HG01346.hp2 HG01891.hp1 HG02109.hp1 others(33): Show |
intron_variant | MODIFIER | c.123-23970G>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51142742 | |||||||
| chr12:51143043 | C | T | 6 | a0001c0001t0001g0317 a0001c0001t0001g0318 a0001c0001t0001g0319 others(3): Show |
6 | HG01884.hp2 HG02723.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.123-24271G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51143043 | |||||||
| chr12:51143064 | C | A | 11 | a0001c0001t0002g0138 a0001c0001t0002g0222 a0001c0001t0002g0280 others(8): Show |
11 | HG00738.hp1 HG01081.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.123-24292G>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51143064 | |||||||
| chr12:51143065 | C | G | 1 | a0001c0001t0001g0272 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.123-24293G>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51143065 | |||||||
| chr12:51143066 | T | C | 3 | a0001c0001t0008g0115 a0001c0001t0008g0116 a0001c0001t0008g0117 |
3 | NA19003.hp1 NA19011.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.123-24294A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51143066 | |||||||
| chr12:51143131 | C | G | 216 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(213): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.123-24359G>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51143131 | |||||||
| chr12:51143239 | T | G | 3 | a0001c0001t0016g0204 a0001c0001t0017g0199 a0001c0001t0017g0203 |
3 | HG00140.hp1 HG02698.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.123-24467A>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51143239 | |||||||
| chr12:51143304 | ATAAC | A | 7 | a0001c0001t0001g0145 a0001c0001t0001g0212 a0001c0001t0001g0292 others(4): Show |
7 | HG01891.hp1 HG02258.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.123-24536_123-2453 others(8): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51143304 | |||||||
| chr12:51143413 | C | T | 208 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(205): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.123-24641G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51143413 | |||||||
| chr12:51143509 | G | T | 3 | a0001c0001t0006g0200 a0001c0001t0006g0201 a0001c0001t0006g0202 |
3 | HG02976.hp1 HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.123-24737C>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51143509 | |||||||
| chr12:51143526 | A | G | 57 | a0001c0001t0003g0002 a0001c0001t0003g0010 a0001c0001t0003g0011 others(54): Show |
58 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.123-24754T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51143526 | |||||||
| chr12:51143848 | A | G | 272 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(269): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.123-25076T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51143848 | |||||||
| chr12:51143856 | A | T | 1 | a0001c0001t0002g0304 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.123-25084T>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51143856 | |||||||
| chr12:51143950 | G | A | 328 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(325): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.123-25178C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51143950 | |||||||
| chr12:51144121 | C | T | 1 | a0001c0001t0016g0206 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.123-25349G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51144121 | |||||||
| chr12:51144291 | T | C | 1 | a0001c0001t0002g0237 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.123-25519A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51144291 | |||||||
| chr12:51144515 | T | C | 1 | a0001c0001t0013g0006 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.123-25743A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51144515 | |||||||
| chr12:51144553 | G | C | 20 | a0001c0001t0005g0118 a0001c0001t0005g0119 a0001c0001t0005g0120 others(17): Show |
20 | HG01346.hp2 HG02145.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.123-25781C>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51144553 | |||||||
| chr12:51144832 | C | A | 2 | a0001c0001t0016g0206 a0001c0001t0031g0146 |
2 | NA18747.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.123-26060G>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51144832 | |||||||
| chr12:51144975 | C | T | 54 | a0001c0001t0004g0003 a0001c0001t0004g0004 a0001c0001t0004g0005 others(51): Show |
57 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.123-26203G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51144975 | |||||||
| chr12:51145103 | A | T | 1 | a0001c0001t0001g0257 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.123-26331T>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51145103 | |||||||
| chr12:51145116 | G | A | 5 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 others(2): Show |
5 | HG02717.hp2 HG03041.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.123-26344C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51145116 | |||||||
| chr12:51145139 | T | C | 1 | a0001c0001t0016g0302 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.123-26367A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51145139 | |||||||
| chr12:51145143 | G | C | 2 | a0001c0001t0016g0206 a0001c0001t0031g0146 |
2 | NA18747.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.123-26371C>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51145143 | |||||||
| chr12:51145150 | G | A | 1 | a0001c0001t0001g0306 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.123-26378C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51145150 | |||||||
| chr12:51145177 | G | A | 213 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(210): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.123-26405C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51145177 | |||||||
| chr12:51145200 | CA | C | 9 | a0001c0001t0001g0229 a0001c0001t0001g0243 a0001c0001t0004g0082 others(6): Show |
10 | HG01069.hp1 HG01071.hp2 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.123-26429delT | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51145200 | |||||||
| chr12:51145200 | CAA | C | 75 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(72): Show |
76 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.123-26430_123-2642 others(6): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51145200 | |||||||
| chr12:51145200 | CAAA | C | 195 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(192): Show |
200 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.123-26431_123-2642 others(7): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51145200 | |||||||
| chr12:51145297 | G | C | 4 | a0001c0001t0001g0164 a0001c0001t0001g0212 a0001c0001t0001g0292 others(1): Show |
4 | HG02055.hp1 HG02647.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-26525C>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51145297 | |||||||
| chr12:51145308 | G | C | 146 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(143): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.123-26536C>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51145308 | |||||||
| chr12:51145393 | A | AAAATAC | 56 | a0001c0001t0003g0002 a0001c0001t0003g0010 a0001c0001t0003g0011 others(53): Show |
57 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.123-26627_123-2662 others(10): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51145393 | |||||||
| chr12:51145456 | C | T | 56 | a0001c0001t0003g0002 a0001c0001t0003g0010 a0001c0001t0003g0011 others(53): Show |
57 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.123-26684G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51145456 | |||||||
| chr12:51145479 | T | C | 4 | a0001c0001t0002g0298 a0001c0001t0002g0299 a0001c0001t0002g0300 others(1): Show |
4 | HG02109.hp1 HG03471.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-26707A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51145479 | |||||||
| chr12:51145526 | A | T | 171 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(168): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.123-26754T>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51145526 | |||||||
| chr12:51145567 | C | CA | 51 | a0001c0001t0001g0293 a0001c0001t0001g0296 a0001c0001t0004g0003 others(48): Show |
55 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.122+26733dupT | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51145567 | |||||||
| chr12:51145567 | C | CAA | 9 | a0001c0001t0004g0097 a0001c0001t0004g0098 a0001c0001t0004g0099 others(6): Show |
9 | HG00735.hp2 HG01361.hp2 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.122+26732_122+2673 others(6): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51145567 | |||||||
| chr12:51145567 | CA | C | 7 | a0001c0001t0002g0180 a0001c0001t0002g0298 a0001c0001t0002g0300 others(4): Show |
7 | HG00735.hp1 HG03471.hp2 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.122+26733delT | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51145567 | |||||||
| chr12:51145567 | CAA | C | 34 | a0001c0001t0001g0220 a0001c0001t0001g0308 a0001c0001t0002g0138 others(31): Show |
34 | HG00609.hp1 HG00733.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.122+26732_122+2673 others(6): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51145567 | |||||||
| chr12:51145567 | CAAA | C | 205 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(202): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.122+26731_122+2673 others(7): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51145567 | |||||||
| chr12:51145567 | CAAAA | C | 20 | a0001c0001t0001g0164 a0001c0001t0001g0212 a0001c0001t0001g0221 others(17): Show |
21 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.122+26730_122+2673 others(8): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51145567 | |||||||
| chr12:51145677 | G | T | 1 | a0001c0001t0004g0077 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.122+26624C>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51145677 | |||||||
| chr12:51145725 | G | A | 206 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(203): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.122+26576C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51145725 | |||||||
| chr12:51146078 | T | A | 331 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(328): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.122+26223A>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51146078 | |||||||
| chr12:51146235 | T | A | 1 | a0001c0001t0018g0009 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.122+26066A>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51146235 | |||||||
| chr12:51146237 | G | A | 2 | a0001c0001t0001g0210 a0001c0001t0001g0241 |
2 | HG03834.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.122+26064C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51146237 | |||||||
| chr12:51146590 | T | C | 1 | a0001c0001t0001g0234 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.122+25711A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51146590 | |||||||
| chr12:51146606 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.122+25695G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51146606 | |||||||
| chr12:51146833 | T | C | 5 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 others(2): Show |
5 | HG02717.hp2 HG03041.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.122+25468A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51146833 | |||||||
| chr12:51146927 | A | C | 1 | a0001c0001t0016g0302 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.122+25374T>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51146927 | |||||||
| chr12:51146959 | C | A | 1 | a0001c0001t0013g0297 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.122+25342G>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51146959 | |||||||
| chr12:51147001 | T | C | 1 | a0001c0001t0001g0230 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.122+25300A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51147001 | |||||||
| chr12:51147081 | G | A | 1 | a0001c0001t0009g0076 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.122+25220C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51147081 | |||||||
| chr12:51147274 | C | CAGAGGTT others(1350): Show |
1 | a0001c0001t0001g0211 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.122+25026_122+2502 others(1361): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51147274 | |||||||
| chr12:51147283 | T | C | 275 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(272): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.122+25018A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51147283 | |||||||
| chr12:51147341 | G | A | 331 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(328): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.122+24960C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51147341 | |||||||
| chr12:51147456 | A | C | 1 | a0001c0001t0003g0033 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.122+24845T>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51147456 | |||||||
| chr12:51147529 | T | TG | 86 | a0001c0001t0001g0164 a0001c0001t0001g0212 a0001c0001t0001g0276 others(83): Show |
87 | HG00140.hp1 HG00280.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.122+24771dupC | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51147529 | |||||||
| chr12:51147537 | GA | G | 5 | a0001c0001t0002g0290 a0001c0001t0002g0298 a0001c0001t0002g0300 others(2): Show |
5 | HG01167.hp1 HG01169.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.122+24763delT | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51147537 | |||||||
| chr12:51147538 | A | G | 1 | a0001c0001t0005g0126 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.122+24763T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51147538 | |||||||
| chr12:51147696 | G | C | 6 | a0001c0001t0001g0317 a0001c0001t0001g0318 a0001c0001t0001g0319 others(3): Show |
6 | HG01884.hp2 HG02723.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.122+24605C>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51147696 | |||||||
| chr12:51148126 | T | TA | 7 | a0001c0001t0001g0317 a0001c0001t0001g0318 a0001c0001t0001g0319 others(4): Show |
7 | HG01884.hp2 HG02523.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.122+24174dupT | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51148126 | |||||||
| chr12:51148150 | G | C | 2 | a0001c0001t0001g0292 a0001c0001t0017g0303 |
2 | HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.122+24151C>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51148150 | |||||||
| chr12:51148269 | C | T | 165 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(162): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.122+24032G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51148269 | |||||||
| chr12:51148419 | G | A | 53 | a0001c0001t0004g0003 a0001c0001t0004g0004 a0001c0001t0004g0005 others(50): Show |
56 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.122+23882C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51148419 | |||||||
| chr12:51148477 | G | A | 263 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(260): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.122+23824C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51148477 | |||||||
| chr12:51148484 | A | G | 54 | a0001c0001t0004g0003 a0001c0001t0004g0004 a0001c0001t0004g0005 others(51): Show |
57 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.122+23817T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51148484 | |||||||
| chr12:51148491 | G | A | 56 | a0001c0001t0004g0003 a0001c0001t0004g0004 a0001c0001t0004g0005 others(53): Show |
59 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.122+23810C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51148491 | |||||||
| chr12:51148561 | G | A | 2 | a0001c0001t0001g0292 a0001c0001t0017g0303 |
2 | HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.122+23740C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51148561 | |||||||
| chr12:51148643 | T | C | 1 | a0001c0002t0004g0071 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.122+23658A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51148643 | |||||||
| chr12:51148699 | C | CA | 183 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(180): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.122+23601dupT | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51148699 | |||||||
| chr12:51148699 | C | CAA | 6 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0002g0280 others(3): Show |
6 | HG02109.hp1 HG02622.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.122+23600_122+2360 others(6): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51148699 | |||||||
| chr12:51148699 | C | CAAAAA | 19 | a0001c0001t0005g0118 a0001c0001t0005g0119 a0001c0001t0005g0120 others(16): Show |
19 | HG01069.hp2 HG01346.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.122+23597_122+2360 others(9): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51148699 | |||||||
| chr12:51148705 | A | G | 15 | a0001c0001t0003g0021 a0001c0001t0003g0023 a0001c0001t0003g0024 others(12): Show |
15 | HG00408.hp1 HG00609.hp1 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.122+23596T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51148705 | |||||||
| chr12:51148712 | A | AG | 3 | a0001c0001t0002g0169 a0001c0001t0002g0183 a0001c0001t0010g0168 |
3 | HG00639.hp2 HG00741.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.122+23588_122+2358 others(5): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51148712 | |||||||
| chr12:51148845 | C | A | 1 | a0001c0001t0003g0044 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.122+23456G>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51148845 | |||||||
| chr12:51148845 | C | T | 4 | a0001c0001t0018g0009 a0001c0001t0018g0335 a0001c0001t0024g0066 others(1): Show |
5 | HG01069.hp1 HG01071.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.122+23456G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51148845 | |||||||
| chr12:51148981 | C | T | 20 | a0001c0001t0005g0118 a0001c0001t0005g0119 a0001c0001t0005g0120 others(17): Show |
20 | HG01069.hp2 HG01346.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.122+23320G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51148981 | |||||||
| chr12:51148988 | G | A | 1 | a0001c0001t0016g0302 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.122+23313C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51148988 | |||||||
| chr12:51149024 | C | CAAAAAAA | 6 | a0001c0001t0002g0290 a0001c0001t0002g0298 a0001c0001t0002g0299 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.122+23270_122+2327 others(11): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51149024 | |||||||
| chr12:51149024 | C | CAAAAAAA others(3): Show |
34 | a0001c0001t0002g0156 a0001c0001t0003g0002 a0001c0001t0003g0010 others(31): Show |
35 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.122+23267_122+2327 others(14): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51149024 | |||||||
| chr12:51149024 | C | CAAAAAAA others(4): Show |
23 | a0001c0001t0003g0016 a0001c0001t0003g0023 a0001c0001t0003g0024 others(20): Show |
23 | HG01168.hp1 HG01358.hp2 HG02027.hp1 others(20): Show |
intron_variant | MODIFIER | c.122+23266_122+2327 others(15): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51149024 | |||||||
| chr12:51149024 | C | CAAAAAAA others(5): Show |
27 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0258 others(24): Show |
28 | HG00423.hp1 HG00609.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.122+23265_122+2327 others(16): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51149024 | |||||||
| chr12:51149024 | C | CAAAAAAA others(6): Show |
75 | a0001c0001t0001g0008 a0001c0001t0001g0147 a0001c0001t0001g0148 others(72): Show |
79 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.122+23264_122+2327 others(17): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51149024 | |||||||
| chr12:51149024 | C | CAAAAAAA others(7): Show |
35 | a0001c0001t0001g0152 a0001c0001t0001g0207 a0001c0001t0001g0210 others(32): Show |
35 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(32): Show |
intron_variant | MODIFIER | c.122+23263_122+2327 others(18): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51149024 | |||||||
| chr12:51149024 | C | CAAAAAAA others(8): Show |
19 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0231 others(16): Show |
19 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.122+23262_122+2327 others(19): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51149024 | |||||||
| chr12:51149024 | C | CAAAAAAA others(9): Show |
1 | a0001c0001t0001g0235 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.122+23261_122+2327 others(20): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51149024 | |||||||
| chr12:51149024 | C | CAAAAAAA others(11): Show |
13 | a0001c0001t0005g0119 a0001c0001t0005g0121 a0001c0001t0005g0122 others(10): Show |
13 | HG01346.hp2 HG02451.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.122+23276_122+2327 others(22): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51149024 | |||||||
| chr12:51149024 | C | CAAAAAAA others(12): Show |
6 | a0001c0001t0005g0120 a0001c0001t0005g0125 a0001c0001t0005g0131 others(3): Show |
6 | HG01069.hp2 HG02145.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.122+23276_122+2327 others(23): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51149024 | |||||||
| chr12:51149024 | C | CAAAAAAA others(21): Show |
1 | a0001c0001t0005g0118 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.122+23276_122+2327 others(32): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51149024 | |||||||
| chr12:51149163 | A | G | 20 | a0001c0001t0005g0118 a0001c0001t0005g0119 a0001c0001t0005g0120 others(17): Show |
20 | HG01069.hp2 HG01346.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.122+23138T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51149163 | |||||||
| chr12:51149401 | T | C | 3 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0002g0304 |
3 | HG02258.hp1 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.122+22900A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51149401 | |||||||
| chr12:51149448 | C | G | 147 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(144): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.122+22853G>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51149448 | |||||||
| chr12:51149618 | G | A | 53 | a0001c0001t0004g0003 a0001c0001t0004g0004 a0001c0001t0004g0005 others(50): Show |
56 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.122+22683C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51149618 | |||||||
| chr12:51149648 | A | G | 275 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(272): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.122+22653T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51149648 | |||||||
| chr12:51150031 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.122+22270G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51150031 | |||||||
| chr12:51150193 | G | A | 57 | a0001c0001t0003g0017 a0001c0001t0004g0003 a0001c0001t0004g0004 others(54): Show |
60 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.122+22108C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51150193 | |||||||
| chr12:51150238 | C | T | 1 | a0001c0001t0004g0069 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.122+22063G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51150238 | |||||||
| chr12:51150333 | G | A | 36 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(33): Show |
36 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.122+21968C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51150333 | |||||||
| chr12:51150417 | C | T | 1 | a0001c0001t0010g0198 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.122+21884G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51150417 | |||||||
| chr12:51150436 | A | T | 2 | a0001c0001t0001g0139 a0001c0001t0001g0140 |
2 | NA18939.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.122+21865T>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51150436 | |||||||
| chr12:51150444 | T | A | 1 | a0001c0001t0018g0335 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.122+21857A>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51150444 | |||||||
| chr12:51150521 | C | T | 275 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(272): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.122+21780G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51150521 | |||||||
| chr12:51150652 | G | C | 1 | a0001c0001t0003g0056 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.122+21649C>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51150652 | |||||||
| chr12:51150735 | T | A | 5 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 others(2): Show |
5 | HG02717.hp2 HG03041.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.122+21566A>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51150735 | |||||||
| chr12:51150756 | T | C | 231 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(228): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.122+21545A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51150756 | |||||||
| chr12:51150786 | C | T | 27 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(24): Show |
27 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.122+21515G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51150786 | |||||||
| chr12:51150829 | C | T | 1 | a0001c0001t0001g0325 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.122+21472G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51150829 | |||||||
| chr12:51150988 | G | C | 2 | a0001c0001t0004g0110 a0001c0001t0004g0114 |
2 | NA18946.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.122+21313C>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51150988 | |||||||
| chr12:51151034 | C | T | 274 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(271): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.122+21267G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51151034 | |||||||
| chr12:51151072 | T | C | 2 | a0001c0001t0003g0010 a0001c0001t0003g0011 |
2 | HG01081.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.122+21229A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51151072 | |||||||
| chr12:51151408 | C | T | 11 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 others(8): Show |
11 | HG01167.hp1 HG01169.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.122+20893G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51151408 | |||||||
| chr12:51151423 | A | G | 1 | a0001c0001t0003g0060 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.122+20878T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51151423 | |||||||
| chr12:51151506 | G | A | 5 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 others(2): Show |
5 | HG02717.hp2 HG03041.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.122+20795C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51151506 | |||||||
| chr12:51151519 | C | T | 11 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 others(8): Show |
11 | HG01167.hp1 HG01169.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.122+20782G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51151519 | |||||||
| chr12:51151573 | A | T | 3 | a0001c0001t0006g0200 a0001c0001t0006g0201 a0001c0001t0006g0202 |
3 | HG02976.hp1 HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.122+20728T>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51151573 | |||||||
| chr12:51151637 | C | T | 53 | a0001c0001t0004g0003 a0001c0001t0004g0004 a0001c0001t0004g0005 others(50): Show |
56 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.122+20664G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51151637 | |||||||
| chr12:51151679 | G | A | 11 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 others(8): Show |
11 | HG01167.hp1 HG01169.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.122+20622C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51151679 | |||||||
| chr12:51151682 | C | T | 5 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 others(2): Show |
5 | HG02717.hp2 HG03041.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.122+20619G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51151682 | |||||||
| chr12:51151688 | G | A | 1 | a0001c0001t0003g0068 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.122+20613C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51151688 | |||||||
| chr12:51151726 | A | G | 331 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(328): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.122+20575T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51151726 | |||||||
| chr12:51151728 | G | A | 77 | a0001c0001t0003g0002 a0001c0001t0003g0010 a0001c0001t0003g0011 others(74): Show |
78 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.122+20573C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51151728 | |||||||
| chr12:51151997 | G | C | 1 | a0001c0001t0001g0236 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.122+20304C>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51151997 | |||||||
| chr12:51152096 | C | T | 20 | a0001c0001t0005g0118 a0001c0001t0005g0119 a0001c0001t0005g0120 others(17): Show |
20 | HG01069.hp2 HG01346.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.122+20205G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51152096 | |||||||
| chr12:51152217 | C | T | 3 | a0001c0001t0001g0213 a0001c0001t0001g0245 a0001c0001t0002g0214 |
3 | NA18971.hp2 NA18984.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.122+20084G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51152217 | |||||||
| chr12:51152303 | A | G | 8 | a0001c0001t0001g0292 a0001c0001t0001g0317 a0001c0001t0001g0318 others(5): Show |
8 | HG01884.hp2 HG02723.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.122+19998T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51152303 | |||||||
| chr12:51152307 | C | T | 57 | a0001c0001t0003g0002 a0001c0001t0003g0010 a0001c0001t0003g0011 others(54): Show |
58 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.122+19994G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51152307 | |||||||
| chr12:51152355 | A | AGATTAAA others(1): Show |
57 | a0001c0001t0003g0002 a0001c0001t0003g0010 a0001c0001t0003g0011 others(54): Show |
58 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.122+19945_122+1994 others(12): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51152355 | |||||||
| chr12:51152358 | A | G | 57 | a0001c0001t0003g0002 a0001c0001t0003g0010 a0001c0001t0003g0011 others(54): Show |
58 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.122+19943T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51152358 | |||||||
| chr12:51152359 | C | A | 57 | a0001c0001t0003g0002 a0001c0001t0003g0010 a0001c0001t0003g0011 others(54): Show |
58 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.122+19942G>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51152359 | |||||||
| chr12:51152412 | T | C | 1 | a0001c0001t0003g0063 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.122+19889A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51152412 | |||||||
| chr12:51152450 | C | G | 1 | a0001c0001t0022g0336 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.122+19851G>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51152450 | |||||||
| chr12:51152542 | G | C | 165 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(162): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.122+19759C>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51152542 | |||||||
| chr12:51152589 | C | T | 3 | a0001c0001t0006g0200 a0001c0001t0006g0201 a0001c0001t0006g0202 |
3 | HG02976.hp1 HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.122+19712G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51152589 | |||||||
| chr12:51152660 | A | C | 165 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(162): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.122+19641T>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51152660 | |||||||
| chr12:51152765 | A | T | 1 | a0001c0001t0016g0302 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.122+19536T>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51152765 | |||||||
| chr12:51152868 | T | C | 6 | a0001c0001t0001g0317 a0001c0001t0001g0318 a0001c0001t0001g0319 others(3): Show |
6 | HG01884.hp2 HG02723.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.122+19433A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51152868 | |||||||
| chr12:51153029 | G | T | 1 | a0001c0001t0003g0057 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.122+19272C>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51153029 | |||||||
| chr12:51153234 | G | A | 3 | a0001c0001t0002g0169 a0001c0001t0002g0183 a0001c0001t0010g0168 |
3 | HG00639.hp2 HG00741.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.122+19067C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51153234 | |||||||
| chr12:51153398 | CT | C | 54 | a0001c0001t0004g0003 a0001c0001t0004g0004 a0001c0001t0004g0005 others(51): Show |
57 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.122+18902delA | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51153398 | |||||||
| chr12:51153398 | CTT | C | 269 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(266): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.122+18901_122+1890 others(6): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51153398 | |||||||
| chr12:51153404 | T | G | 27 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(24): Show |
27 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.122+18897A>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51153404 | |||||||
| chr12:51153404 | TTTTTTTG | T | 5 | a0001c0001t0018g0009 a0001c0001t0018g0335 a0001c0001t0024g0066 others(2): Show |
6 | HG01069.hp1 HG01071.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.122+18890_122+1889 others(11): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51153404 | |||||||
| chr12:51153519 | T | C | 77 | a0001c0001t0003g0002 a0001c0001t0003g0010 a0001c0001t0003g0011 others(74): Show |
78 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.122+18782A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51153519 | |||||||
| chr12:51153566 | A | ACT | 275 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(272): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.122+18733_122+1873 others(6): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51153566 | |||||||
| chr12:51153697 | A | G | 1 | a0001c0001t0001g0248 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.122+18604T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51153697 | |||||||
| chr12:51153697 | A | T | 274 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(271): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.122+18604T>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51153697 | |||||||
| chr12:51153714 | T | C | 270 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(267): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.122+18587A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51153714 | |||||||
| chr12:51153753 | T | C | 16 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(13): Show |
16 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.122+18548A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51153753 | |||||||
| chr12:51153759 | A | G | 11 | a0001c0001t0001g0292 a0001c0001t0001g0305 a0001c0001t0001g0306 others(8): Show |
11 | HG01884.hp2 HG02258.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.122+18542T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51153759 | |||||||
| chr12:51153890 | C | T | 20 | a0001c0001t0005g0118 a0001c0001t0005g0119 a0001c0001t0005g0120 others(17): Show |
20 | HG01069.hp2 HG01346.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.122+18411G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51153890 | |||||||
| chr12:51153948 | C | G | 165 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(162): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.122+18353G>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51153948 | |||||||
| chr12:51154046 | AT | A | 275 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(272): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.122+18254delA | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51154046 | |||||||
| chr12:51154222 | A | G | 1 | a0001c0001t0027g0244 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.122+18079T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51154222 | |||||||
| chr12:51154318 | T | C | 1 | a0001c0001t0016g0302 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.122+17983A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51154318 | |||||||
| chr12:51154368 | A | C | 27 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(24): Show |
27 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.122+17933T>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51154368 | |||||||
| chr12:51154465 | G | A | 1 | a0001c0001t0002g0307 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.122+17836C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51154465 | |||||||
| chr12:51154490 | T | C | 1 | a0001c0001t0002g0307 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.122+17811A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51154490 | |||||||
| chr12:51154541 | G | A | 331 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(328): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.122+17760C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51154541 | |||||||
| chr12:51154555 | G | A | 1 | a0001c0001t0006g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.122+17746C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51154555 | |||||||
| chr12:51154617 | C | A | 20 | a0001c0001t0005g0118 a0001c0001t0005g0119 a0001c0001t0005g0120 others(17): Show |
20 | HG01069.hp2 HG01346.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.122+17684G>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51154617 | |||||||
| chr12:51154824 | G | C | 1 | a0001c0001t0016g0302 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.122+17477C>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51154824 | |||||||
| chr12:51154840 | C | T | 274 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(271): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.122+17461G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51154840 | |||||||
| chr12:51154856 | C | A | 1 | a0001c0001t0002g0300 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.122+17445G>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51154856 | |||||||
| chr12:51154861 | T | A | 1 | a0001c0001t0002g0237 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.122+17440A>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51154861 | |||||||
| chr12:51154921 | G | C | 1 | a0001c0001t0001g0250 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.122+17380C>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51154921 | |||||||
| chr12:51155078 | A | G | 20 | a0001c0001t0005g0118 a0001c0001t0005g0119 a0001c0001t0005g0120 others(17): Show |
20 | HG01069.hp2 HG01346.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.122+17223T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51155078 | |||||||
| chr12:51155228 | G | A | 20 | a0001c0001t0005g0118 a0001c0001t0005g0119 a0001c0001t0005g0120 others(17): Show |
20 | HG01069.hp2 HG01346.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.122+17073C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51155228 | |||||||
| chr12:51155315 | C | G | 1 | a0001c0001t0002g0281 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.122+16986G>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51155315 | |||||||
| chr12:51155347 | C | A | 1 | a0001c0001t0001g0292 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.122+16954G>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51155347 | |||||||
| chr12:51155500 | A | G | 1 | a0001c0001t0018g0009 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.122+16801T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51155500 | |||||||
| chr12:51155670 | TATAATCC others(5): Show |
T | 1 | a0001c0001t0001g0152 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.122+16619_122+1663 others(16): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51155670 | |||||||
| chr12:51155730 | A | G | 2 | a0001c0001t0024g0066 a0001c0001t0032g0334 |
2 | HG02630.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.122+16571T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51155730 | |||||||
| chr12:51155734 | A | G | 2 | a0001c0001t0002g0184 a0001c0001t0002g0185 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.122+16567T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51155734 | |||||||
| chr12:51155914 | T | C | 194 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(191): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.122+16387A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51155914 | |||||||
| chr12:51155968 | G | C | 8 | a0001c0001t0004g0005 a0001c0001t0004g0108 a0001c0001t0004g0109 others(5): Show |
9 | HG00544.hp2 HG02523.hp1 NA18947.hp1 others(6): Show |
intron_variant | MODIFIER | c.122+16333C>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51155968 | |||||||
| chr12:51156045 | CA | C | 6 | a0001c0001t0004g0074 a0001c0001t0004g0080 a0001c0001t0004g0102 others(3): Show |
6 | HG00438.hp2 HG01934.hp2 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.122+16255delT | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51156045 | |||||||
| chr12:51156045 | CAA | C | 50 | a0001c0001t0004g0003 a0001c0001t0004g0004 a0001c0001t0004g0005 others(47): Show |
53 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.122+16254_122+1625 others(6): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51156045 | |||||||
| chr12:51156045 | CAAAAAAA others(6): Show |
C | 19 | a0001c0001t0005g0118 a0001c0001t0005g0119 a0001c0001t0005g0120 others(16): Show |
19 | HG01069.hp2 HG01346.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.122+16243_122+1625 others(17): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51156045 | |||||||
| chr12:51156045 | CAAAAAAA others(7): Show |
C | 256 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(253): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.122+16242_122+1625 others(18): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51156045 | |||||||
| chr12:51156123 | C | G | 1 | a0001c0001t0001g0212 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.122+16178G>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51156123 | |||||||
| chr12:51156138 | T | C | 11 | a0001c0001t0001g0292 a0001c0001t0001g0305 a0001c0001t0001g0306 others(8): Show |
11 | HG01884.hp2 HG02258.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.122+16163A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51156138 | |||||||
| chr12:51156343 | A | AG | 58 | a0001c0001t0002g0280 a0001c0001t0003g0002 a0001c0001t0003g0010 others(55): Show |
59 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.122+15957dupC | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51156343 | |||||||
| chr12:51156348 | G | C | 3 | a0001c0001t0001g0238 a0001c0001t0002g0205 a0001c0001t0002g0239 |
3 | NA18612.hp1 NA18947.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.122+15953C>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51156348 | |||||||
| chr12:51156364 | T | C | 1 | a0001c0001t0002g0173 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.122+15937A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51156364 | |||||||
| chr12:51156475 | C | G | 2 | a0001c0001t0004g0069 a0001c0001t0004g0070 |
2 | NA18995.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.122+15826G>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51156475 | |||||||
| chr12:51156577 | G | A | 3 | a0001c0001t0002g0298 a0001c0001t0002g0299 a0001c0001t0002g0300 |
3 | HG02109.hp1 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.122+15724C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51156577 | |||||||
| chr12:51156637 | GTTC | G | 57 | a0001c0001t0003g0002 a0001c0001t0003g0010 a0001c0001t0003g0011 others(54): Show |
58 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.122+15661_122+1566 others(7): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51156637 | |||||||
| chr12:51156908 | G | GC | 11 | a0001c0001t0001g0292 a0001c0001t0001g0305 a0001c0001t0001g0306 others(8): Show |
11 | HG01884.hp2 HG02258.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.122+15392_122+1539 others(5): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51156908 | |||||||
| chr12:51156909 | T | A | 11 | a0001c0001t0001g0292 a0001c0001t0001g0305 a0001c0001t0001g0306 others(8): Show |
11 | HG01884.hp2 HG02258.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.122+15392A>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51156909 | |||||||
| chr12:51156995 | G | C | 275 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(272): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.122+15306C>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51156995 | |||||||
| chr12:51157017 | TC | T | 274 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(271): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.122+15283delG | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51157017 | |||||||
| chr12:51157018 | C | T | 1 | a0001c0001t0001g0250 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.122+15283G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51157018 | |||||||
| chr12:51157019 | T | C | 1 | a0001c0001t0001g0250 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.122+15282A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51157019 | |||||||
| chr12:51157020 | T | C | 274 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(271): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.122+15281A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51157020 | |||||||
| chr12:51157071 | A | G | 149 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(146): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.122+15230T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51157071 | |||||||
| chr12:51157273 | CAGCCTCC others(3): Show |
C | 2 | a0001c0001t0007g0331 a0001c0001t0007g0332 |
2 | HG02818.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.122+15018_122+1502 others(14): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51157273 | |||||||
| chr12:51157439 | C | T | 275 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(272): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.122+14862G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51157439 | |||||||
| chr12:51157450 | G | A | 1 | a0001c0001t0003g0021 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.122+14851C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51157450 | |||||||
| chr12:51157464 | TG | T | 18 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0150 others(15): Show |
21 | HG00140.hp2 HG00639.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.122+14836delC | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51157464 | |||||||
| chr12:51157469 | T | C | 20 | a0001c0001t0005g0118 a0001c0001t0005g0119 a0001c0001t0005g0120 others(17): Show |
20 | HG01069.hp2 HG01346.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.122+14832A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51157469 | |||||||
| chr12:51157540 | C | T | 8 | a0001c0001t0001g0292 a0001c0001t0001g0317 a0001c0001t0001g0318 others(5): Show |
8 | HG01884.hp2 HG02723.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.122+14761G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51157540 | |||||||
| chr12:51157681 | C | CT | 54 | a0001c0001t0001g0148 a0001c0001t0002g0154 a0001c0001t0002g0299 others(51): Show |
55 | HG00280.hp2 HG00408.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.122+14619dupA | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51157681 | |||||||
| chr12:51157681 | C | CTT | 143 | a0001c0001t0001g0008 a0001c0001t0001g0140 a0001c0001t0001g0147 others(140): Show |
149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.122+14618_122+1461 others(6): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51157681 | |||||||
| chr12:51157681 | C | CTTT | 20 | a0001c0001t0001g0139 a0001c0001t0001g0152 a0001c0001t0001g0164 others(17): Show |
20 | HG01109.hp2 HG01167.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.122+14617_122+1461 others(7): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51157681 | |||||||
| chr12:51157681 | C | T | 9 | a0001c0001t0001g0292 a0001c0001t0001g0306 a0001c0001t0001g0317 others(6): Show |
9 | HG01884.hp2 HG02723.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.122+14620G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51157681 | |||||||
| chr12:51157681 | CTTTTCT | C | 20 | a0001c0001t0005g0118 a0001c0001t0005g0119 a0001c0001t0005g0120 others(17): Show |
20 | HG01069.hp2 HG01346.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.122+14614_122+1461 others(10): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51157681 | |||||||
| chr12:51157685 | TC | T | 4 | a0001c0001t0018g0335 a0001c0001t0024g0066 a0001c0001t0031g0146 others(1): Show |
4 | HG02559.hp1 HG02630.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.122+14615delG | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51157685 | |||||||
| chr12:51157686 | C | CTT | 6 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(3): Show |
6 | HG01891.hp1 HG02451.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.122+14613_122+1461 others(6): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51157686 | |||||||
| chr12:51157686 | C | T | 243 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(240): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.122+14615G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51157686 | |||||||
| chr12:51157686 | CT | C | 53 | a0001c0001t0004g0003 a0001c0001t0004g0004 a0001c0001t0004g0005 others(50): Show |
56 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.122+14614delA | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51157686 | |||||||
| chr12:51157838 | G | A | 3 | a0001c0001t0002g0298 a0001c0001t0002g0299 a0001c0001t0002g0300 |
3 | HG02109.hp1 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.122+14463C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51157838 | |||||||
| chr12:51157897 | C | A | 57 | a0001c0001t0003g0002 a0001c0001t0003g0010 a0001c0001t0003g0011 others(54): Show |
58 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.122+14404G>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51157897 | |||||||
| chr12:51157996 | C | T | 19 | a0001c0001t0005g0118 a0001c0001t0005g0119 a0001c0001t0005g0120 others(16): Show |
19 | HG01069.hp2 HG01346.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.122+14305G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51157996 | |||||||
| chr12:51158057 | T | C | 1 | a0001c0001t0016g0302 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.122+14244A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51158057 | |||||||
| chr12:51158073 | C | A | 11 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 others(8): Show |
11 | HG01167.hp1 HG01169.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.122+14228G>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51158073 | |||||||
| chr12:51158177 | T | C | 1 | a0001c0001t0005g0121 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.122+14124A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51158177 | |||||||
| chr12:51158211 | T | C | 1 | a0001c0001t0033g0338 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.122+14090A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51158211 | |||||||
| chr12:51158396 | G | C | 1 | a0001c0001t0002g0239 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.122+13905C>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51158396 | |||||||
| chr12:51158578 | T | G | 1 | a0001c0001t0001g0240 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.122+13723A>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51158578 | |||||||
| chr12:51158605 | C | T | 4 | a0001c0001t0001g0211 a0001c0001t0003g0028 a0001c0001t0003g0051 others(1): Show |
4 | HG01255.hp2 HG01361.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.122+13696G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51158605 | |||||||
| chr12:51158654 | A | G | 5 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0210 others(2): Show |
5 | HG03834.hp1 NA18949.hp1 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.122+13647T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51158654 | |||||||
| chr12:51158749 | A | T | 1 | a0001c0001t0022g0337 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.122+13552T>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51158749 | |||||||
| chr12:51158842 | C | T | 1 | a0001c0001t0001g0272 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.122+13459G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51158842 | |||||||
| chr12:51158891 | C | A | 1 | a0001c0001t0016g0204 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.122+13410G>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51158891 | |||||||
| chr12:51158918 | C | A | 11 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0121 others(8): Show |
11 | HG01346.hp2 HG02145.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.122+13383G>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51158918 | |||||||
| chr12:51159005 | T | TA | 3 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0002g0304 |
3 | HG02258.hp1 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.122+13295_122+1329 others(5): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51159005 | |||||||
| chr12:51159005 | TCC | T | 181 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(178): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.122+13294_122+1329 others(6): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51159005 | |||||||
| chr12:51159005 | TCCA | T | 25 | a0001c0001t0001g0272 a0001c0001t0001g0277 a0001c0001t0002g0165 others(22): Show |
25 | HG01069.hp2 HG01192.hp2 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.122+13293_122+1329 others(7): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51159005 | |||||||
| chr12:51159005 | TCCAA | T | 42 | a0001c0001t0003g0002 a0001c0001t0003g0010 a0001c0001t0003g0011 others(39): Show |
43 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.122+13292_122+1329 others(8): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51159005 | |||||||
| chr12:51159006 | C | A | 85 | a0001c0001t0001g0153 a0001c0001t0001g0241 a0001c0001t0001g0243 others(82): Show |
88 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.122+13295G>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51159006 | |||||||
| chr12:51159007 | C | A | 3 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0002g0304 |
3 | HG02258.hp1 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.122+13294G>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51159007 | |||||||
| chr12:51159007 | CA | C | 73 | a0001c0001t0001g0153 a0001c0001t0001g0241 a0001c0001t0001g0243 others(70): Show |
75 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.122+13293delT | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51159007 | |||||||
| chr12:51159009 | A | C | 181 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(178): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.122+13292T>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51159009 | |||||||
| chr12:51159010 | A | C | 25 | a0001c0001t0001g0272 a0001c0001t0001g0277 a0001c0001t0002g0165 others(22): Show |
25 | HG01069.hp2 HG01192.hp2 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.122+13291T>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51159010 | |||||||
| chr12:51159011 | A | C | 42 | a0001c0001t0003g0002 a0001c0001t0003g0010 a0001c0001t0003g0011 others(39): Show |
43 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.122+13290T>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51159011 | |||||||
| chr12:51159093 | C | A | 275 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(272): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.122+13208G>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51159093 | |||||||
| chr12:51159095 | T | C | 275 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(272): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.122+13206A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51159095 | |||||||
| chr12:51159178 | C | CA | 158 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(155): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.122+13122dupT | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51159178 | |||||||
| chr12:51159195 | GA | G | 55 | a0001c0001t0001g0271 a0001c0001t0004g0003 a0001c0001t0004g0004 others(52): Show |
58 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.122+13105delT | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51159195 | |||||||
| chr12:51159237 | T | C | 8 | a0001c0001t0001g0292 a0001c0001t0001g0317 a0001c0001t0001g0318 others(5): Show |
8 | HG01884.hp2 HG02723.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.122+13064A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51159237 | |||||||
| chr12:51159253 | A | G | 2 | a0001c0001t0002g0290 a0001c0001t0002g0301 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.122+13048T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51159253 | |||||||
| chr12:51159346 | A | AT | 15 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(12): Show |
15 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.122+12954dupA | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51159346 | |||||||
| chr12:51159374 | G | A | 3 | a0001c0001t0002g0156 a0001c0001t0013g0006 a0001c0001t0013g0155 |
4 | HG01109.hp1 HG02723.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.122+12927C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51159374 | |||||||
| chr12:51159528 | G | A | 136 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(133): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.122+12773C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51159528 | |||||||
| chr12:51159575 | C | T | 1 | a0001c0001t0028g0330 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.122+12726G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51159575 | |||||||
| chr12:51159597 | C | T | 1 | a0001c0001t0006g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.122+12704G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51159597 | |||||||
| chr12:51159762 | C | T | 1 | a0001c0001t0004g0080 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.122+12539G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51159762 | |||||||
| chr12:51159874 | C | T | 2 | a0001c0001t0001g0258 a0001c0001t0001g0259 |
2 | HG00423.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.122+12427G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51159874 | |||||||
| chr12:51160133 | A | AT | 144 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(141): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.122+12167dupA | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51160133 | |||||||
| chr12:51160133 | A | ATT | 7 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0002g0175 others(4): Show |
7 | HG00438.hp1 HG01175.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.122+12166_122+1216 others(6): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51160133 | |||||||
| chr12:51160133 | AT | A | 17 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0145 others(14): Show |
17 | HG01891.hp1 HG01943.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.122+12167delA | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51160133 | |||||||
| chr12:51160133 | ATT | A | 78 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0292 others(75): Show |
79 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.122+12166_122+1216 others(6): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51160133 | |||||||
| chr12:51160133 | ATTT | A | 10 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0002g0298 others(7): Show |
10 | HG02109.hp1 HG02258.hp1 HG03209.hp1 others(7): Show |
intron_variant | MODIFIER | c.122+12165_122+1216 others(7): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51160133 | |||||||
| chr12:51160281 | G | A | 21 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(18): Show |
21 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.122+12020C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51160281 | |||||||
| chr12:51160370 | C | T | 1 | a0001c0001t0004g0077 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.122+11931G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51160370 | |||||||
| chr12:51160424 | C | G | 10 | a0001c0001t0002g0138 a0001c0001t0002g0280 a0001c0001t0002g0281 others(7): Show |
10 | HG00738.hp1 HG01081.hp1 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.122+11877G>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51160424 | |||||||
| chr12:51160537 | T | A | 1 | a0001c0001t0004g0113 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.122+11764A>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51160537 | |||||||
| chr12:51160887 | T | C | 1 | a0001c0001t0001g0250 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.122+11414A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51160887 | |||||||
| chr12:51160944 | G | A | 1 | a0001c0001t0031g0146 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.122+11357C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51160944 | |||||||
| chr12:51161010 | C | T | 1 | a0001c0001t0016g0302 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.122+11291G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51161010 | |||||||
| chr12:51161014 | T | G | 21 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(18): Show |
21 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.122+11287A>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51161014 | |||||||
| chr12:51161043 | A | G | 159 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(156): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.122+11258T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51161043 | |||||||
| chr12:51161057 | G | C | 1 | a0001c0001t0032g0334 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.122+11244C>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51161057 | |||||||
| chr12:51161073 | T | C | 18 | a0001c0001t0001g0292 a0001c0001t0001g0293 a0001c0001t0001g0294 others(15): Show |
18 | HG01167.hp1 HG01169.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.122+11228A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51161073 | |||||||
| chr12:51161359 | G | C | 1 | a0001c0001t0022g0337 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.122+10942C>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51161359 | |||||||
| chr12:51161381 | G | GA | 36 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(33): Show |
36 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.122+10919dupT | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51161381 | |||||||
| chr12:51161446 | C | T | 40 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(37): Show |
40 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.122+10855G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51161446 | |||||||
| chr12:51161472 | A | G | 18 | a0001c0001t0001g0292 a0001c0001t0001g0293 a0001c0001t0001g0294 others(15): Show |
18 | HG01167.hp1 HG01169.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.122+10829T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51161472 | |||||||
| chr12:51161679 | C | CA | 159 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(156): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.122+10621dupT | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51161679 | |||||||
| chr12:51161688 | T | A | 169 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(166): Show |
175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.122+10613A>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51161688 | |||||||
| chr12:51161691 | T | A | 30 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(27): Show |
31 | HG01069.hp1 HG01071.hp2 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.122+10610A>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51161691 | |||||||
| chr12:51161718 | G | A | 259 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(256): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.122+10583C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51161718 | |||||||
| chr12:51161752 | C | T | 1 | a0001c0001t0031g0146 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.122+10549G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51161752 | |||||||
| chr12:51161760 | CA | C | 73 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0249 others(70): Show |
76 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.122+10540delT | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51161760 | |||||||
| chr12:51161760 | CAA | C | 92 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(89): Show |
93 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.122+10539_122+1054 others(6): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51161760 | |||||||
| chr12:51161760 | CAAA | C | 141 | a0001c0001t0001g0164 a0001c0001t0001g0292 a0001c0001t0001g0293 others(138): Show |
147 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.122+10538_122+1054 others(7): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51161760 | |||||||
| chr12:51161760 | CAAAA | C | 18 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(15): Show |
18 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.122+10537_122+1054 others(8): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51161760 | |||||||
| chr12:51161760 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0003g0021 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.122+10528_122+1054 others(17): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51161760 | |||||||
| chr12:51161778 | A | G | 1 | a0001c0001t0026g0186 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.122+10523T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51161778 | |||||||
| chr12:51161883 | C | T | 259 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(256): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.122+10418G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51161883 | |||||||
| chr12:51161904 | C | CA | 9 | a0001c0001t0004g0005 a0001c0001t0004g0108 a0001c0001t0004g0109 others(6): Show |
10 | HG00544.hp2 HG02523.hp1 HG06807.hp2 others(7): Show |
intron_variant | MODIFIER | c.122+10396dupT | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51161904 | |||||||
| chr12:51161908 | C | A | 289 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(286): Show |
296 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.122+10393G>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51161908 | |||||||
| chr12:51162107 | T | C | 1 | a0001c0001t0001g0276 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.122+10194A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51162107 | |||||||
| chr12:51162142 | C | T | 7 | a0001c0001t0001g0292 a0001c0001t0002g0290 a0001c0001t0002g0298 others(4): Show |
7 | HG01167.hp1 HG01169.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.122+10159G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51162142 | |||||||
| chr12:51162203 | T | C | 1 | a0001c0001t0003g0065 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.122+10098A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51162203 | |||||||
| chr12:51162208 | G | A | 60 | a0001c0001t0003g0002 a0001c0001t0003g0010 a0001c0001t0003g0011 others(57): Show |
61 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.122+10093C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51162208 | |||||||
| chr12:51162303 | A | G | 331 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(328): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.122+9998T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51162303 | |||||||
| chr12:51162322 | T | C | 260 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(257): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.122+9979A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51162322 | |||||||
| chr12:51162337 | G | A | 1 | a0001c0001t0017g0303 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.122+9964C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51162337 | |||||||
| chr12:51162402 | C | T | 4 | a0001c0001t0003g0024 a0001c0001t0003g0025 a0001c0001t0003g0026 others(1): Show |
4 | NA18949.hp2 NA18982.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.122+9899G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51162402 | |||||||
| chr12:51162445 | C | CA | 74 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(71): Show |
75 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.122+9855dupT | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51162445 | |||||||
| chr12:51162761 | C | T | 7 | a0001c0001t0002g0157 a0001c0001t0002g0162 a0001c0001t0002g0163 others(4): Show |
7 | HG01070.hp2 HG01071.hp1 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.122+9540G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51162761 | |||||||
| chr12:51162980 | G | T | 18 | a0001c0001t0001g0292 a0001c0001t0001g0293 a0001c0001t0001g0294 others(15): Show |
18 | HG01167.hp1 HG01169.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.122+9321C>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51162980 | |||||||
| chr12:51163282 | C | G | 18 | a0001c0001t0001g0292 a0001c0001t0001g0293 a0001c0001t0001g0294 others(15): Show |
18 | HG01167.hp1 HG01169.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.122+9019G>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51163282 | |||||||
| chr12:51163287 | C | G | 3 | a0001c0001t0002g0311 a0001c0001t0006g0309 a0001c0001t0006g0310 |
3 | HG02109.hp2 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.122+9014G>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51163287 | |||||||
| chr12:51163311 | C | T | 71 | a0001c0001t0004g0003 a0001c0001t0004g0004 a0001c0001t0004g0005 others(68): Show |
74 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.122+8990G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51163311 | |||||||
| chr12:51163317 | C | T | 1 | a0001c0001t0004g0075 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.122+8984G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51163317 | |||||||
| chr12:51163505 | G | A | 2 | a0001c0001t0004g0005 a0001c0001t0018g0009 |
4 | HG01069.hp1 HG01071.hp2 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.122+8796C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51163505 | |||||||
| chr12:51163619 | A | G | 1 | a0001c0001t0002g0157 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.122+8682T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51163619 | |||||||
| chr12:51163674 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.122+8627G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51163674 | |||||||
| chr12:51163698 | A | G | 260 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(257): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.122+8603T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51163698 | |||||||
| chr12:51163741 | G | A | 1 | a0001c0001t0002g0307 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.122+8560C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51163741 | |||||||
| chr12:51163882 | A | C | 3 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0002g0304 |
3 | HG02258.hp1 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.122+8419T>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51163882 | |||||||
| chr12:51164142 | G | A | 2 | a0001c0001t0004g0110 a0001c0001t0004g0114 |
2 | NA18946.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.122+8159C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51164142 | |||||||
| chr12:51164181 | G | A | 60 | a0001c0001t0003g0002 a0001c0001t0003g0010 a0001c0001t0003g0011 others(57): Show |
61 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.122+8120C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51164181 | |||||||
| chr12:51164193 | C | T | 160 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(157): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.122+8108G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51164193 | |||||||
| chr12:51164239 | C | T | 3 | a0001c0001t0002g0156 a0001c0001t0013g0006 a0001c0001t0013g0155 |
4 | HG01109.hp1 HG02723.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.122+8062G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51164239 | |||||||
| chr12:51164267 | G | A | 1 | a0001c0001t0002g0251 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.122+8034C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51164267 | |||||||
| chr12:51164336 | C | T | 6 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(3): Show |
6 | HG01891.hp1 HG02451.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.122+7965G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51164336 | |||||||
| chr12:51164370 | G | A | 1 | a0001c0001t0017g0303 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.122+7931C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51164370 | |||||||
| chr12:51164597 | G | A | 53 | a0001c0001t0004g0003 a0001c0001t0004g0004 a0001c0001t0004g0005 others(50): Show |
56 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.122+7704C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51164597 | |||||||
| chr12:51164597 | G | GA | 62 | a0001c0001t0001g0145 a0001c0001t0001g0288 a0001c0001t0003g0002 others(59): Show |
63 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.122+7703dupT | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51164597 | |||||||
| chr12:51164597 | GA | G | 7 | a0001c0001t0002g0154 a0001c0001t0002g0307 a0001c0001t0007g0331 others(4): Show |
7 | HG01884.hp1 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.122+7703delT | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51164597 | |||||||
| chr12:51164868 | T | C | 12 | a0001c0001t0001g0292 a0001c0001t0001g0293 a0001c0001t0001g0294 others(9): Show |
12 | HG01167.hp1 HG01169.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.122+7433A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51164868 | |||||||
| chr12:51164929 | C | T | 12 | a0001c0001t0001g0292 a0001c0001t0001g0293 a0001c0001t0001g0294 others(9): Show |
12 | HG01167.hp1 HG01169.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.122+7372G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51164929 | |||||||
| chr12:51164948 | A | G | 1 | a0001c0001t0004g0074 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.122+7353T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51164948 | |||||||
| chr12:51165070 | T | G | 1 | a0001c0001t0002g0254 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.122+7231A>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51165070 | |||||||
| chr12:51165110 | T | C | 1 | a0001c0001t0002g0307 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.122+7191A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51165110 | |||||||
| chr12:51165142 | T | C | 18 | a0001c0001t0005g0118 a0001c0001t0005g0119 a0001c0001t0005g0120 others(15): Show |
18 | HG01069.hp2 HG01346.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.122+7159A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51165142 | |||||||
| chr12:51165172 | T | C | 60 | a0001c0001t0003g0002 a0001c0001t0003g0010 a0001c0001t0003g0011 others(57): Show |
61 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.122+7129A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51165172 | |||||||
| chr12:51165201 | C | T | 259 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(256): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.122+7100G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51165201 | |||||||
| chr12:51165357 | T | A | 1 | a0001c0001t0002g0307 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.122+6944A>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51165357 | |||||||
| chr12:51165445 | T | TA | 27 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(24): Show |
27 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.122+6855dupT | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51165445 | |||||||
| chr12:51165602 | G | T | 1 | a0001c0001t0013g0297 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.122+6699C>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51165602 | |||||||
| chr12:51165636 | A | G | 1 | a0001c0001t0013g0297 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.122+6665T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51165636 | |||||||
| chr12:51165728 | A | G | 60 | a0001c0001t0003g0002 a0001c0001t0003g0010 a0001c0001t0003g0011 others(57): Show |
61 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.122+6573T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51165728 | |||||||
| chr12:51165733 | T | A | 3 | a0001c0001t0018g0009 a0001c0001t0018g0335 a0001c0001t0032g0334 |
4 | HG01069.hp1 HG01071.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.122+6568A>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51165733 | |||||||
| chr12:51165915 | G | A | 1 | a0001c0001t0001g0255 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.122+6386C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51165915 | |||||||
| chr12:51166088 | G | A | 159 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(156): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.122+6213C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51166088 | |||||||
| chr12:51166144 | G | A | 16 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(13): Show |
16 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.122+6157C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51166144 | |||||||
| chr12:51166343 | T | C | 155 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(152): Show |
160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.122+5958A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51166343 | |||||||
| chr12:51166452 | A | G | 3 | a0001c0001t0004g0003 a0001c0001t0004g0072 a0001c0001t0004g0073 |
4 | HG02258.hp2 HG02486.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.122+5849T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51166452 | |||||||
| chr12:51166522 | C | G | 22 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(19): Show |
22 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.122+5779G>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51166522 | |||||||
| chr12:51166550 | A | G | 1 | a0001c0001t0016g0302 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.122+5751T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51166550 | |||||||
| chr12:51166554 | G | C | 12 | a0001c0001t0001g0151 a0001c0001t0001g0256 a0001c0001t0001g0257 others(9): Show |
12 | HG00423.hp1 HG00438.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.122+5747C>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51166554 | |||||||
| chr12:51167018 | T | C | 1 | a0001c0001t0002g0307 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.122+5283A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51167018 | |||||||
| chr12:51167086 | T | G | 1 | a0001c0001t0004g0112 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.122+5215A>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51167086 | |||||||
| chr12:51167087 | G | T | 1 | a0001c0001t0004g0112 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.122+5214C>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51167087 | |||||||
| chr12:51167088 | T | G | 1 | a0001c0001t0004g0112 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.122+5213A>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51167088 | |||||||
| chr12:51167106 | A | G | 1 | a0001c0001t0013g0297 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.122+5195T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51167106 | |||||||
| chr12:51167273 | C | T | 259 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(256): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.122+5028G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51167273 | |||||||
| chr12:51167384 | G | A | 159 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(156): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.122+4917C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51167384 | |||||||
| chr12:51167395 | T | G | 1 | a0001c0001t0001g0267 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.122+4906A>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51167395 | |||||||
| chr12:51167399 | AT | A | 236 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(233): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.122+4901delA | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51167399 | |||||||
| chr12:51167478 | C | T | 1 | a0001c0001t0016g0302 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.122+4823G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51167478 | |||||||
| chr12:51167504 | T | A | 1 | a0001c0001t0004g0113 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.122+4797A>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51167504 | |||||||
| chr12:51167535 | G | C | 1 | a0001c0001t0001g0306 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.122+4766C>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51167535 | |||||||
| chr12:51167610 | C | G | 18 | a0001c0001t0001g0292 a0001c0001t0001g0293 a0001c0001t0001g0294 others(15): Show |
18 | HG01167.hp1 HG01169.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.122+4691G>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51167610 | |||||||
| chr12:51167790 | G | A | 60 | a0001c0001t0003g0002 a0001c0001t0003g0010 a0001c0001t0003g0011 others(57): Show |
61 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.122+4511C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51167790 | |||||||
| chr12:51167800 | T | A | 1 | a0001c0001t0024g0066 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.122+4501A>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51167800 | |||||||
| chr12:51168002 | A | G | 1 | a0001c0001t0001g0276 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.122+4299T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51168002 | |||||||
| chr12:51168056 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.122+4245G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51168056 | |||||||
| chr12:51168094 | TA | T | 259 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(256): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.122+4206delT | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51168094 | |||||||
| chr12:51168155 | G | A | 7 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0140 others(4): Show |
8 | HG02155.hp1 NA18939.hp1 NA18951.hp1 others(5): Show |
intron_variant | MODIFIER | c.122+4146C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51168155 | |||||||
| chr12:51168279 | C | T | 1 | a0001c0002t0004g0071 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.122+4022G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51168279 | |||||||
| chr12:51168301 | G | T | 1 | a0001c0001t0002g0307 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.122+4000C>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51168301 | |||||||
| chr12:51168339 | G | C | 20 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0001g0308 others(17): Show |
20 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.122+3962C>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51168339 | |||||||
| chr12:51168361 | GAGCCACT others(7): Show |
G | 7 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(4): Show |
7 | HG00597.hp1 HG02056.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.122+3926_122+3939d others(16): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51168361 | |||||||
| chr12:51168727 | T | C | 1 | a0001c0001t0006g0316 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.122+3574A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51168727 | |||||||
| chr12:51168748 | T | G | 17 | a0001c0001t0005g0118 a0001c0001t0005g0122 a0001c0001t0005g0123 others(14): Show |
17 | HG01069.hp2 HG01346.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.122+3553A>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51168748 | |||||||
| chr12:51168809 | AT | A | 172 | a0001c0001t0001g0275 a0001c0001t0001g0292 a0001c0001t0001g0293 others(169): Show |
176 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.122+3491delA | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51168809 | |||||||
| chr12:51168842 | C | T | 1 | a0001c0001t0001g0151 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.122+3459G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51168842 | |||||||
| chr12:51168873 | C | T | 7 | a0001c0001t0001g0292 a0001c0001t0002g0290 a0001c0001t0002g0298 others(4): Show |
7 | HG01167.hp1 HG01169.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.122+3428G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51168873 | |||||||
| chr12:51168884 | T | C | 78 | a0001c0001t0004g0003 a0001c0001t0004g0004 a0001c0001t0004g0005 others(75): Show |
81 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.122+3417A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51168884 | |||||||
| chr12:51168887 | C | T | 1 | a0001c0001t0002g0150 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.122+3414G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51168887 | |||||||
| chr12:51168925 | C | G | 1 | a0001c0001t0005g0118 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.122+3376G>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51168925 | |||||||
| chr12:51168976 | A | G | 3 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 |
3 | NA18983.hp2 NA19002.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.122+3325T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51168976 | |||||||
| chr12:51169182 | T | C | 4 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0002g0304 others(1): Show |
4 | HG02258.hp1 HG02622.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.122+3119A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51169182 | |||||||
| chr12:51169245 | T | C | 2 | a0001c0001t0001g0276 a0001c0001t0001g0277 |
2 | HG02630.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.122+3056A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51169245 | |||||||
| chr12:51169276 | G | A | 1 | a0001c0001t0016g0302 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.122+3025C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51169276 | |||||||
| chr12:51169358 | G | A | 1 | a0001c0001t0001g0278 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.122+2943C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51169358 | |||||||
| chr12:51169363 | T | C | 6 | a0001c0001t0001g0317 a0001c0001t0001g0318 a0001c0001t0001g0319 others(3): Show |
6 | HG01884.hp2 HG02723.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.122+2938A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51169363 | |||||||
| chr12:51169371 | T | C | 60 | a0001c0001t0003g0002 a0001c0001t0003g0010 a0001c0001t0003g0011 others(57): Show |
61 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.122+2930A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51169371 | |||||||
| chr12:51169383 | G | C | 171 | a0001c0001t0001g0292 a0001c0001t0001g0293 a0001c0001t0001g0294 others(168): Show |
175 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.122+2918C>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51169383 | |||||||
| chr12:51169578 | C | G | 1 | a0001c0001t0031g0146 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.122+2723G>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51169578 | |||||||
| chr12:51169584 | G | A | 1 | a0001c0001t0029g0279 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.122+2717C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51169584 | |||||||
| chr12:51169639 | C | T | 3 | a0001c0001t0008g0115 a0001c0001t0008g0116 a0001c0001t0008g0117 |
3 | NA19003.hp1 NA19011.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.122+2662G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51169639 | |||||||
| chr12:51169645 | C | A | 1 | a0001c0001t0002g0287 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.122+2656G>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51169645 | |||||||
| chr12:51169873 | C | T | 5 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(2): Show |
5 | HG01891.hp1 HG02451.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.122+2428G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51169873 | |||||||
| chr12:51169907 | G | A | 3 | a0001c0001t0002g0298 a0001c0001t0002g0299 a0001c0001t0002g0300 |
3 | HG02109.hp1 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.122+2394C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51169907 | |||||||
| chr12:51170296 | A | G | 3 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0002g0304 |
3 | HG02258.hp1 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.122+2005T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51170296 | |||||||
| chr12:51170343 | C | CTTTTTTT others(1): Show |
60 | a0001c0001t0002g0301 a0001c0001t0003g0002 a0001c0001t0003g0013 others(57): Show |
61 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.122+1950_122+1957d others(10): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51170343 | |||||||
| chr12:51170343 | C | CTTTTTTT others(2): Show |
105 | a0001c0001t0001g0292 a0001c0001t0001g0293 a0001c0001t0001g0294 others(102): Show |
108 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.122+1949_122+1957d others(11): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51170343 | |||||||
| chr12:51170343 | C | CTTTTTTT others(3): Show |
4 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0002g0304 others(1): Show |
4 | HG02258.hp1 HG02622.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.122+1957_122+1958i others(12): Show |
TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51170343 | |||||||
| chr12:51170343 | C | T | 1 | a0001c0001t0016g0302 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.122+1958G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51170343 | |||||||
| chr12:51170405 | A | G | 1 | a0001c0001t0013g0006 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.122+1896T>C | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51170405 | |||||||
| chr12:51170583 | C | T | 1 | a0001c0001t0017g0303 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.122+1718G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51170583 | |||||||
| chr12:51170609 | T | C | 21 | a0001c0001t0005g0118 a0001c0001t0005g0119 a0001c0001t0005g0120 others(18): Show |
21 | HG01069.hp2 HG01346.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.122+1692A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51170609 | |||||||
| chr12:51170676 | T | C | 21 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0001g0308 others(18): Show |
21 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.122+1625A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51170676 | |||||||
| chr12:51170686 | T | C | 11 | a0001c0001t0002g0138 a0001c0001t0002g0280 a0001c0001t0002g0281 others(8): Show |
11 | HG00738.hp1 HG01081.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.122+1615A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51170686 | |||||||
| chr12:51170817 | T | C | 1 | a0001c0001t0001g0288 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.122+1484A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51170817 | |||||||
| chr12:51170920 | C | T | 2 | a0001c0001t0001g0139 a0001c0001t0001g0140 |
2 | NA18939.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.122+1381G>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51170920 | |||||||
| chr12:51170968 | G | A | 1 | a0001c0001t0021g0289 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.122+1333C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51170968 | |||||||
| chr12:51170995 | A | T | 1 | a0001c0001t0002g0138 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.122+1306T>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51170995 | |||||||
| chr12:51171019 | T | A | 172 | a0001c0001t0001g0292 a0001c0001t0001g0293 a0001c0001t0001g0294 others(169): Show |
176 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.122+1282A>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51171019 | |||||||
| chr12:51171336 | A | T | 2 | a0001c0001t0004g0069 a0001c0001t0004g0070 |
2 | NA18995.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.122+965T>A | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51171336 | |||||||
| chr12:51171503 | G | C | 1 | a0001c0001t0002g0324 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.122+798C>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51171503 | |||||||
| chr12:51171581 | T | C | 78 | a0001c0001t0004g0003 a0001c0001t0004g0004 a0001c0001t0004g0005 others(75): Show |
81 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.122+720A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51171581 | |||||||
| chr12:51171685 | G | A | 2 | a0001c0001t0015g0136 a0001c0001t0015g0137 |
2 | NA18971.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.122+616C>T | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51171685 | |||||||
| chr12:51171836 | T | C | 62 | a0001c0001t0001g0325 a0001c0001t0001g0326 a0001c0001t0003g0002 others(59): Show |
63 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.122+465A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51171836 | |||||||
| chr12:51171871 | T | C | 3 | a0001c0001t0002g0327 a0001c0001t0002g0329 a0001c0001t0006g0328 |
3 | HG03130.hp1 HG03139.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.122+430A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51171871 | |||||||
| chr12:51172109 | T | C | 78 | a0001c0001t0004g0003 a0001c0001t0004g0004 a0001c0001t0004g0005 others(75): Show |
81 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.122+192A>G | TFCP2 | ENSG00000135457.11 | transcript | ENST00000257915.10 | protein_coding | 1/14 | chr12 | 51172109 |