| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:90001392-90001544 | Rare:70 | ||||
| chr8:90985192-90985418 | Common:4; Rare:70 | ||||
| chr8:91070007-91070425 | Common:1; Rare:150 | ||||
| chr8:92095221-92095358 | Rare:35 | ||||
| chr8:92966016-92966216 | Rare:34 | ||||
| chr8:93700466-93700630 | Common:1; Rare:67 | ||||
| chr8:93754784-93754947 | Common:1; Rare:64; Clinvar:1; Clinvar (benign):5 | ||||
| chr8:93916675-93917001 | Common:3; Rare:113; Clinvar:1; Clinvar (benign):1 | ||||
| chr8:94553443-94553739 | Common:3; Rare:105 | ||||
| chr8:94719834-94719955 | Common:1; Rare:39 | ||||
| chr8:94895197-94895322 | Rare:41 | ||||
| chr8:94895639-94895806 | Rare:48 | ||||
| chr8:94949362-94949567 | Common:2; Rare:60 | ||||
| chr8:95268491-95268849 | Common:10; Rare:75 | ||||
| chr8:96235510-96235649 | Common:1; Rare:73; Clinvar (benign):2 |