| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:108534148-108534502 | Common:7; Rare:142 | ||||
| chr2:108719345-108719593 | Common:3; Rare:113; Clinvar (benign):2 | ||||
| chr2:110204961-110205063 | Rare:45; Clinvar:1 | ||||
| chr2:110677997-110678258 | Rare:88 | ||||
| chr2:111884091-111884257 | Rare:48 | ||||
| chr2:111898308-111898611 | Common:2; Rare:67 | ||||
| chr2:112254998-112255173 | Common:1; Rare:77 | ||||
| chr2:112542140-112542493 | Common:1; Rare:109 | ||||
| chr2:112584393-112584633 | Common:1; Rare:65 | ||||
| chr2:112645609-112645966 | Common:2; Rare:128 | ||||
| chr2:113437728-113437904 | Common:3; Rare:78 | ||||
| chr2:113627046-113627277 | Common:1; Rare:68 | ||||
| chr2:113756601-113756791 | Common:3; Rare:74 | ||||
| chr2:113889710-113890210 | Common:8; Rare:158 | ||||
| chr2:118014040-118014214 | Common:2; Rare:99 |