| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:71356486-71356811 | Rare:78; Clinvar:1; Clinvar (benign):1 | ||||
| chr8:71361763-71361928 | Common:1; Rare:49; Clinvar:4; Clinvar (benign):2 | ||||
| chr8:71362096-71362330 | Common:1; Rare:31 | ||||
| chr8:71843844-71844323 | Common:1; Rare:173 | ||||
| chr8:73008636-73008910 | Common:1; Rare:94 | ||||
| chr8:73292679-73293156 | Common:3; Rare:154 | ||||
| chr8:73293396-73293399 | |||||
| chr8:73293579-73293724 | Rare:77 | ||||
| chr8:73293882-73294119 | Common:1; Rare:74 | ||||
| chr8:73294139-73294281 | Common:1; Rare:43 | ||||
| chr8:73294354-73294605 | Common:1; Rare:83 | ||||
| chr8:73878811-73879009 | Common:3; Rare:96 | ||||
| chr8:73971880-73971957 | Rare:27 | ||||
| chr8:73972060-73972618 | Common:2; Rare:154 | ||||
| chr8:73976038-73976360 | Common:5; Rare:120; Clinvar:3; Clinvar (benign):4 |