| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:121530579-121530884 | Common:7; Rare:127 | ||||
| chr2:121649418-121649683 | Common:2; Rare:77 | ||||
| chr2:121736846-121737249 | Common:5; Rare:151 | ||||
| chr2:121755379-121755780 | Common:6; Rare:133 | ||||
| chr2:124025167-124025320 | Common:2; Rare:53 | ||||
| chr2:127294088-127294203 | Common:2; Rare:44; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:127526435-127526596 | Common:2; Rare:50 | ||||
| chr2:127645996-127646153 | Rare:36 | ||||
| chr2:127811139-127811224 | Rare:28 | ||||
| chr2:127858102-127858182 | Rare:47 | ||||
| chr2:128028023-128028254 | Common:1; Rare:66 | ||||
| chr2:128091054-128091335 | Common:8; Rare:95 | ||||
| chr2:130181546-130181795 | Common:3; Rare:111 | ||||
| chr2:130342111-130342228 | Rare:51; Clinvar:1 | ||||
| chr2:130342692-130342935 | Common:3; Rare:80 |