| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:100150555-100150701 | Rare:47 | ||||
| chr8:100310055-100310355 | Common:1; Rare:126 | ||||
| chr8:100706531-100706707 | Common:2; Rare:41 | ||||
| chr8:100706714-100706999 | Common:9; Rare:78 | ||||
| chr8:100709182-100709543 | Common:6; Rare:102 | ||||
| chr8:100709719-100709894 | Common:1; Rare:47 | ||||
| chr8:100712359-100712791 | Common:2; Rare:120 | ||||
| chr8:100712877-100713179 | Common:8; Rare:61 | ||||
| chr8:100950550-100950722 | Common:8; Rare:86 | ||||
| chr8:100951462-100951793 | Common:2; Rare:117 | ||||
| chr8:100952540-100952613 | Rare:23 | ||||
| chr8:100952866-100953435 | Common:5; Rare:136 | ||||
| chr8:101205528-101205881 | Common:4; Rare:115 | ||||
| chr8:102238768-102239090 | Common:6; Rare:123; Clinvar:1; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr8:102412680-102412898 | Common:1; Rare:50 |