Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:228103292-228103491 | Not yet | Common:1; Rare:68 | 179 | ||
chr1:228109247-228109471 | Not yet | Rare:77 | 241 | ||
chr1:228457866-228458107 | Not yet | Common:1; Rare:73 | 269 | ||
chr1:229271036-229271117 | Not yet | Rare:27 | 95 | ||
chr1:229626080-229626251 | Not yet | Rare:59 | 188 | ||
chr1:230867946-230868183 | Not yet | Common:3; Rare:54 | 275 | ||
chr1:230978830-230979117 | Not yet | Common:1; Rare:102 | 329 | ||
chr1:231241087-231241362 | Not yet | Common:2; Rare:134; Clinvar:4; Clinvar (benign):2 | 218 | ||
chr1:231337803-231338048 | Not yet | Common:2; Rare:91 | 232 | ||
chr1:231528613-231528724 | Not yet | Common:1; Rare:48 | 152 | ||
chr1:234373418-234373770 | Not yet | Common:1; Rare:167; Clinvar (benign):7 | 347 | ||
chr1:234608200-234608236 | Not yet | Rare:12 | 55 | ||
chr1:235883265-235883461 | Not yet | Common:1; Rare:28 | 302 | ||
chr1:240091768-240091944 | Not yet | Common:3; Rare:72 | 198 | ||
chr1:243255741-243256137 | Not yet | Common:1; Rare:113; Clinvar:4; Clinvar (benign):1 | 340 |