| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:49623286-49623575 | Common:1; Rare:80 | ||||
| chr12:49828380-49828511 | Common:1; Rare:53 | ||||
| chr12:50025412-50025731 | Common:2; Rare:87 | ||||
| chr12:50085300-50085381 | Common:1; Rare:16 | ||||
| chr12:50103794-50104084 | Rare:74 | ||||
| chr12:50104896-50105176 | Common:1; Rare:53 | ||||
| chr12:50283420-50283692 | Common:3; Rare:83 | ||||
| chr12:50763913-50764126 | Common:1; Rare:61 | ||||
| chr12:50924426-50924743 | Common:3; Rare:85 | ||||
| chr12:51026313-51026545 | Common:3; Rare:99; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:51048098-51048359 | Common:2; Rare:87 | ||||
| chr12:51238648-51238914 | Common:8; Rare:115 | ||||
| chr12:51270170-51270355 | Common:3; Rare:48 | ||||
| chr12:51270371-51270432 | Rare:17 | ||||
| chr12:51391232-51391458 | Common:2; Rare:47 |