| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:100309885-100310319 | Common:1; Rare:162 | ||||
| chr8:100709131-100709733 | Common:11; Rare:149 | ||||
| chr8:100951265-100951416 | Rare:53 | ||||
| chr8:100953336-100953414 | Common:1; Rare:16 | ||||
| chr8:101205444-101205754 | Common:5; Rare:97 | ||||
| chr8:102238832-102238949 | Rare:49; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr8:102239046-102239311 | Common:2; Rare:59 | ||||
| chr8:102412666-102413027 | Common:3; Rare:89 | ||||
| chr8:102655618-102655860 | Common:1; Rare:91 | ||||
| chr8:102864109-102864271 | Common:2; Rare:73 | ||||
| chr8:103298737-103298935 | Common:1; Rare:47 | ||||
| chr8:103414831-103414879 | Rare:12 | ||||
| chr8:103414988-103415511 | Common:6; Rare:256 | ||||
| chr8:106657568-106658004 | Common:5; Rare:120 | ||||
| chr8:107497270-107497537 | Common:2; Rare:73 |