| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:135052208-135052320 | Common:1; Rare:49; Clinvar (benign):1 | ||||
| chr2:135531170-135531526 | Common:1; Rare:74 | ||||
| chr2:135586188-135586496 | Rare:55 | ||||
| chr2:135741528-135741929 | Common:5; Rare:132 | ||||
| chr2:135876357-135876650 | Common:1; Rare:81 | ||||
| chr2:135985404-135985705 | Common:4; Rare:130; Clinvar (benign):1 | ||||
| chr2:136118126-136118283 | Rare:41 | ||||
| chr2:136765421-136765616 | Common:5; Rare:48 | ||||
| chr2:138501658-138502020 | Common:2; Rare:130 | ||||
| chr2:138780239-138780578 | Rare:103 | ||||
| chr2:142130756-142131037 | Common:2; Rare:91 | ||||
| chr2:144332449-144332689 | Rare:96 | ||||
| chr2:144430983-144431111 | Rare:18 | ||||
| chr2:144513791-144513955 | Rare:44 | ||||
| chr2:144517287-144517610 | Common:1; Rare:93; Clinvar:3; Clinvar (benign):5 |