| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:73976029-73976310 | Common:6; Rare:101; Clinvar:3; Clinvar (benign):3 | ||||
| chr8:74350261-74350568 | Common:2; Rare:126; Clinvar:2; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr8:74824321-74824544 | Common:2; Rare:46 | ||||
| chr8:74984428-74984749 | Common:3; Rare:102 | ||||
| chr8:75407879-75407928 | Rare:14 | ||||
| chr8:76681110-76681407 | Common:1; Rare:59 | ||||
| chr8:76683132-76683930 | Common:5; Rare:164 | ||||
| chr8:77000163-77000201 | Common:1; Rare:16; Clinvar:3 | ||||
| chr8:77000203-77000304 | Rare:28 | ||||
| chr8:78665951-78666160 | Rare:82 | ||||
| chr8:80029905-80029986 | Common:1; Rare:28 | ||||
| chr8:80030147-80030304 | Rare:71 | ||||
| chr8:80171373-80171682 | Common:8; Rare:104 | ||||
| chr8:80485580-80485624 | Rare:8 | ||||
| chr8:81280356-81280641 | Common:2; Rare:105 |