| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:89524738-89524904 | Common:2; Rare:31 | ||||
| chr12:89708815-89708992 | Rare:70 | ||||
| chr12:91182612-91182665 | Rare:14 | ||||
| chr12:95003623-95003821 | Common:3; Rare:78; Clinvar (benign):4 | ||||
| chr12:95217465-95217831 | Common:1; Rare:100 | ||||
| chr12:96035548-96035786 | Common:2; Rare:55 | ||||
| chr12:98644717-98644865 | Common:2; Rare:47 | ||||
| chr12:100200707-100200822 | Rare:33 | ||||
| chr12:101407705-101408053 | Common:3; Rare:83 | ||||
| chr12:101877529-101877769 | Common:4; Rare:62 | ||||
| chr12:102120061-102120246 | Rare:70 | ||||
| chr12:103930044-103930508 | Common:8; Rare:158 | ||||
| chr12:103965727-103965987 | Common:2; Rare:55 | ||||
| chr12:104064442-104064566 | Rare:30 | ||||
| chr12:106955526-106955966 | Rare:159 |