| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74529662-74530009 | Rare:102; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:74530361-74530797 | Common:5; Rare:217; Clinvar:7; Clinvar (benign):3 | ||||
| chr2:74553860-74554220 | Rare:71 | ||||
| chr2:74554240-74554540 | Common:2; Rare:70 | ||||
| chr2:74554967-74555367 | Common:1; Rare:117 | ||||
| chr2:74654065-74654314 | Common:1; Rare:71 | ||||
| chr2:74833898-74834147 | Rare:76 | ||||
| chr2:74835129-74835325 | Rare:49 | ||||
| chr2:74958541-74958677 | Common:2; Rare:49 | ||||
| chr2:74958871-74959071 | Rare:72 | ||||
| chr2:75560933-75561068 | Rare:33 | ||||
| chr2:75561116-75561287 | Common:4; Rare:38 | ||||
| chr2:75646728-75646862 | Rare:50 | ||||
| chr2:75647020-75647570 | Common:3; Rare:147 | ||||
| chr2:75710600-75711190 | Common:4; Rare:206 |