| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:111122449-111122763 | Common:3; Rare:128 | ||||
| chr2:111884103-111884268 | Rare:50 | ||||
| chr2:112275404-112275594 | Common:1; Rare:58 | ||||
| chr2:112542148-112542493 | Common:1; Rare:106 | ||||
| chr2:112584410-112584639 | Common:1; Rare:64 | ||||
| chr2:112584801-112584892 | Rare:19 | ||||
| chr2:112645590-112645951 | Common:2; Rare:124 | ||||
| chr2:112764584-112764779 | Common:1; Rare:63; Clinvar (pathogenic):1 | ||||
| chr2:112836756-112837099 | Common:1; Rare:52; Clinvar:1 | ||||
| chr2:113627041-113627272 | Common:1; Rare:68 | ||||
| chr2:113756556-113756791 | Common:3; Rare:82 | ||||
| chr2:113889704-113890290 | Common:9; Rare:188 | ||||
| chr2:113891008-113891109 | Rare:26 | ||||
| chr2:118014056-118014254 | Common:2; Rare:107 | ||||
| chr2:118088167-118088540 | Common:2; Rare:95 |