| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:85016535-85016665 | Rare:14 | ||||
| chr12:85036230-85036532 | Common:2; Rare:76 | ||||
| chr12:85036546-85036633 | Common:1; Rare:19 | ||||
| chr12:85836278-85836432 | Rare:21 | ||||
| chr12:85836452-85836776 | Common:3; Rare:51 | ||||
| chr12:88035407-88035646 | Common:1; Rare:71 | ||||
| chr12:88035672-88035870 | Rare:64 | ||||
| chr12:88141765-88141953 | Common:2; Rare:33; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:88141970-88142427 | Rare:128; Clinvar:5 | ||||
| chr12:88580044-88580566 | Common:3; Rare:147; Clinvar (benign):1 | ||||
| chr12:89351516-89351907 | Common:2; Rare:139 | ||||
| chr12:89351929-89352083 | Rare:58 | ||||
| chr12:89352191-89352880 | Common:5; Rare:195 | ||||
| chr12:89352982-89353357 | Rare:78 | ||||
| chr12:89353370-89353594 | Rare:56 |