| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:132416279-132416672 | Common:1; Rare:101 | ||||
| chr2:132416677-132416887 | Common:1; Rare:53 | ||||
| chr2:132417102-132417406 | Common:1; Rare:87 | ||||
| chr2:134918585-134918931 | Common:1; Rare:148 | ||||
| chr2:135052167-135052332 | Common:1; Rare:67; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:135531172-135531514 | Common:1; Rare:72 | ||||
| chr2:135741611-135742007 | Common:4; Rare:140 | ||||
| chr2:135742300-135742611 | Rare:66 | ||||
| chr2:135985398-135985704 | Common:4; Rare:130; Clinvar (benign):1 | ||||
| chr2:135985870-135985996 | Common:1; Rare:27 | ||||
| chr2:136118139-136118328 | Rare:49 | ||||
| chr2:137964100-137964624 | Common:2; Rare:99 | ||||
| chr2:138501645-138502077 | Common:4; Rare:153 | ||||
| chr2:142130895-142130971 | Rare:16 | ||||
| chr2:142130981-142131024 | Rare:14 |