| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:108621164-108621280 | Rare:17 | ||||
| chr2:108719352-108719553 | Common:2; Rare:88 | ||||
| chr2:108786685-108786818 | Common:2; Rare:70 | ||||
| chr2:110677997-110678244 | Rare:82 | ||||
| chr2:111884081-111884240 | Common:1; Rare:47 | ||||
| chr2:112255033-112255187 | Common:2; Rare:69 | ||||
| chr2:112584346-112584639 | Common:1; Rare:82 | ||||
| chr2:112645688-112645951 | Common:1; Rare:97 | ||||
| chr2:112764591-112764815 | Common:2; Rare:74; Clinvar (pathogenic):1 | ||||
| chr2:113278919-113279083 | Common:1; Rare:35 | ||||
| chr2:113627065-113627272 | Common:1; Rare:62 | ||||
| chr2:113756566-113756816 | Common:4; Rare:87 | ||||
| chr2:113889782-113890224 | Common:7; Rare:129 | ||||
| chr2:118014062-118014243 | Common:2; Rare:100 | ||||
| chr2:119366788-119367059 | Common:1; Rare:82 |