| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:108534204-108534477 | Common:7; Rare:113 | ||||
| chr2:108719388-108719564 | Common:3; Rare:71; Clinvar (benign):1 | ||||
| chr2:109613885-109613996 | Common:1; Rare:40 | ||||
| chr2:110204934-110205054 | Common:1; Rare:53; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:110678041-110678214 | Rare:44 | ||||
| chr2:111884151-111884255 | Rare:30 | ||||
| chr2:112254999-112255207 | Common:2; Rare:86 | ||||
| chr2:112275399-112275634 | Common:1; Rare:77 | ||||
| chr2:112542148-112542487 | Common:1; Rare:106 | ||||
| chr2:112584303-112584645 | Common:2; Rare:94 | ||||
| chr2:112645701-112645944 | Common:1; Rare:89 | ||||
| chr2:112646253-112646439 | Common:1; Rare:66 | ||||
| chr2:113437642-113437849 | Common:1; Rare:78 | ||||
| chr2:113627009-113627323 | Common:4; Rare:95 | ||||
| chr2:113756566-113756759 | Common:2; Rare:64 |