| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:50763829-50764191 | Common:2; Rare:106 | ||||
| chr12:50764290-50764743 | Common:4; Rare:143 | ||||
| chr12:50924269-50924415 | Rare:20 | ||||
| chr12:50924446-50924740 | Common:3; Rare:82 | ||||
| chr12:51025849-51025925 | Rare:14 | ||||
| chr12:51026297-51026625 | Common:6; Rare:125; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:51047824-51048019 | Common:2; Rare:35 | ||||
| chr12:51048022-51048429 | Common:2; Rare:136 | ||||
| chr12:51083454-51083806 | Common:1; Rare:130 | ||||
| chr12:51172017-51172397 | Common:1; Rare:55 | ||||
| chr12:51172725-51172968 | Common:3; Rare:53 | ||||
| chr12:51173011-51173344 | Rare:66 | ||||
| chr12:51217229-51217650 | Common:2; Rare:94 | ||||
| chr12:51218128-51218441 | Common:5; Rare:63 | ||||
| chr12:51238586-51238972 | Common:8; Rare:155 |