| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:156950112-156950387 | Common:2; Rare:127 | ||||
| chr7:157336746-157337013 | Common:2; Rare:115 | ||||
| chr7:158704784-158704948 | Common:1; Rare:59 | ||||
| chr7:158856527-158856746 | Common:7; Rare:86 | ||||
| chr8:232139-232397 | Common:3; Rare:103 | ||||
| chr8:1755642-1755766 | Common:2; Rare:35 | ||||
| chr8:2127530-2127804 | Common:13; Rare:64 | ||||
| chr8:6406521-6406670 | Common:3; Rare:81; Clinvar:2; Clinvar (benign):1 | ||||
| chr8:6708170-6708396 | Common:3; Rare:101 | ||||
| chr8:6709046-6709214 | Common:2; Rare:70 | ||||
| chr8:9151629-9151734 | Rare:30 | ||||
| chr8:9555884-9555968 | Rare:55 | ||||
| chr8:11769572-11769774 | Common:5; Rare:85 | ||||
| chr8:11802446-11802916 | Common:7; Rare:254 | ||||
| chr8:11802924-11803021 | Rare:60 |