| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:127387928-127388255 | Common:9; Rare:142 | ||||
| chr2:127526450-127526577 | Common:1; Rare:39 | ||||
| chr2:127811145-127811254 | Rare:32 | ||||
| chr2:127885886-127885994 | Rare:28 | ||||
| chr2:128091034-128091354 | Common:8; Rare:103 | ||||
| chr2:130181546-130181780 | Common:3; Rare:105 | ||||
| chr2:130342123-130342218 | Rare:41; Clinvar:1 | ||||
| chr2:130342645-130342930 | Common:5; Rare:89 | ||||
| chr2:131105193-131105375 | Common:1; Rare:84 | ||||
| chr2:131492754-131493092 | Common:8; Rare:101 | ||||
| chr2:134918614-134918852 | Common:1; Rare:97 | ||||
| chr2:135530710-135530988 | Common:3; Rare:66 | ||||
| chr2:135531172-135531502 | Common:1; Rare:66 | ||||
| chr2:135985407-135985685 | Common:4; Rare:123; Clinvar (benign):1 | ||||
| chr2:138501675-138502037 | Common:2; Rare:123 |