| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:123584843-123585243 | Common:2; Rare:115 | ||||
| chr12:123601221-123602389 | Common:43; Rare:806 | ||||
| chr12:123633518-123633962 | Common:13; Rare:869; Clinvar:48; Clinvar (benign):6 | ||||
| chr12:123670852-123671252 | Common:12; Rare:236; Clinvar:3; Clinvar (benign):3 | ||||
| chr12:123712090-123712537 | Common:41; Rare:835; Clinvar:17; Clinvar (benign):14 | ||||
| chr12:123971625-123973317 | Common:31; Rare:1382 | ||||
| chr12:123998206-123998606 | Common:1; Rare:64 | ||||
| chr12:124422505-124423312 | Common:27; Rare:533 | ||||
| chr12:124567101-124567253 | Rare:50 | ||||
| chr12:124567290-124567931 | Common:22; Rare:690 | ||||
| chr12:124863648-124863753 | Common:4; Rare:34 | ||||
| chr12:124863716-124864183 | Common:7; Rare:635 | ||||
| chr12:124913918-124914318 | Common:22; Rare:286 | ||||
| chr12:124914533-124915150 | Common:29; Rare:884 | ||||
| chr12:124915221-124915621 | Common:2; Rare:182 |