| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:100150555-100150701 | Rare:47 | ||||
| chr8:100309914-100310231 | Common:1; Rare:107 | ||||
| chr8:100950427-100950699 | Common:10; Rare:118 | ||||
| chr8:101205591-101205867 | Common:3; Rare:78 | ||||
| chr8:103371406-103371571 | Common:1; Rare:49 | ||||
| chr8:103414999-103415507 | Common:6; Rare:251 | ||||
| chr8:106657541-106657898 | Common:4; Rare:101 | ||||
| chr8:108248690-108248870 | Rare:68 | ||||
| chr8:109334009-109334426 | Common:1; Rare:126 | ||||
| chr8:109539542-109539908 | Common:2; Rare:92 | ||||
| chr8:116766252-116766546 | Common:4; Rare:74 | ||||
| chr8:118951838-118952157 | Common:1; Rare:91; Clinvar:7; Clinvar (benign):1 | ||||
| chr8:119832826-119832897 | Common:1; Rare:25 | ||||
| chr8:120445100-120445467 | Common:1; Rare:96 | ||||
| chr8:122781589-122781659 | Rare:10 |