| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:136115522-136116552 | Common:4; Rare:259; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:136117397-136117866 | Rare:148 | ||||
| chr2:136118137-136118351 | Rare:56 | ||||
| chr2:137964430-137965050 | Rare:147 | ||||
| chr2:138501614-138501808 | Common:3; Rare:83 | ||||
| chr2:138780358-138780530 | Rare:55 | ||||
| chr2:142130816-142131801 | Common:17; Rare:485 | ||||
| chr2:144332165-144332276 | Common:1; Rare:48 | ||||
| chr2:144332430-144332661 | Rare:92 | ||||
| chr2:144513779-144513965 | Rare:47 | ||||
| chr2:144515761-144516845 | Common:16; Rare:483 | ||||
| chr2:144517375-144517775 | Common:5; Rare:135; Clinvar (benign):4 | ||||
| chr2:144520111-144520570 | Common:5; Rare:79; Clinvar (benign):1 | ||||
| chr2:144520759-144521920 | Common:3; Rare:222 | ||||
| chr2:144524422-144524677 | Common:4; Rare:62 |