| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6461751-6462301 | Common:8; Rare:458 | ||||
| chr12:6462633-6463467 | Common:8; Rare:220; Clinvar (benign):1 | ||||
| chr12:6466860-6467023 | Rare:30 | ||||
| chr12:6468798-6469479 | Common:7; Rare:159 | ||||
| chr12:6480049-6480449 | Common:7; Rare:83 | ||||
| chr12:6531216-6532500 | Common:15; Rare:413 | ||||
| chr12:6532600-6533022 | Common:3; Rare:138 | ||||
| chr12:6533147-6533351 | Common:1; Rare:38 | ||||
| chr12:6538567-6538782 | Common:1; Rare:69 | ||||
| chr12:6540020-6540420 | Common:4; Rare:130 | ||||
| chr12:6540616-6540761 | Common:2; Rare:42 | ||||
| chr12:6554110-6554374 | Common:6; Rare:86 | ||||
| chr12:6601653-6602474 | Common:5; Rare:553 | ||||
| chr12:6604395-6606039 | Common:21; Rare:966 | ||||
| chr12:6608071-6608739 | Common:14; Rare:242 |