| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:144412816-144413379 | Common:1; Rare:210; Clinvar:2 | ||||
| chr8:144413511-144413786 | Common:1; Rare:101; Clinvar:1 | ||||
| chr8:144413788-144414000 | Common:1; Rare:87 | ||||
| chr8:144414018-144414310 | Common:5; Rare:116; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr8:144414326-144414620 | Common:1; Rare:101; Clinvar:2; Clinvar (benign):1 | ||||
| chr8:144416066-144416344 | Common:2; Rare:91 | ||||
| chr8:144416483-144416711 | Common:2; Rare:76; Clinvar:1; Clinvar (benign):2 | ||||
| chr8:144416761-144417045 | Common:2; Rare:80; Clinvar:1; Clinvar (benign):1 | ||||
| chr8:144427622-144427975 | Common:2; Rare:99 | ||||
| chr8:144428455-144428638 | Common:2; Rare:68 | ||||
| chr8:144465344-144465493 | Common:3; Rare:58 | ||||
| chr8:144477857-144478104 | Common:5; Rare:93 | ||||
| chr8:144478295-144478473 | Rare:44 | ||||
| chr8:144496084-144496328 | Common:1; Rare:61 | ||||
| chr8:144501043-144501754 | Rare:315 |