| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:96305466-96305607 | Common:1; Rare:50; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:96335680-96335824 | Common:1; Rare:55 | ||||
| chr2:96638284-96638453 | Common:1; Rare:43 | ||||
| chr2:96857899-96858265 | Common:2; Rare:134 | ||||
| chr2:96868561-96868743 | Rare:45 | ||||
| chr2:97094829-97094966 | Common:1; Rare:27 | ||||
| chr2:97645780-97646179 | Common:3; Rare:118 | ||||
| chr2:97663902-97664261 | Common:1; Rare:110 | ||||
| chr2:98608445-98608650 | Common:1; Rare:94 | ||||
| chr2:99154863-99155037 | Common:2; Rare:75; Clinvar (benign):1 | ||||
| chr2:99180967-99181233 | Common:2; Rare:79 | ||||
| chr2:99337345-99337466 | Rare:48 | ||||
| chr2:101002156-101002318 | Rare:63 | ||||
| chr2:101474682-101474821 | Common:1; Rare:23 | ||||
| chr2:102736825-102736951 | Common:1; Rare:63 |