| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6970621-6970966 | Common:4; Rare:108; Clinvar (benign):1 | ||||
| chr12:7189519-7189733 | Rare:73; Clinvar:4 | ||||
| chr12:8032542-8032759 | Common:5; Rare:70 | ||||
| chr12:9115850-9116207 | Common:3; Rare:73 | ||||
| chr12:10098952-10099051 | Common:1; Rare:23 | ||||
| chr12:10613534-10613622 | Rare:36 | ||||
| chr12:10929094-10929324 | Common:2; Rare:59 | ||||
| chr12:11171604-11171705 | Common:1; Rare:34 | ||||
| chr12:12357004-12357098 | Common:1; Rare:47 | ||||
| chr12:12611808-12611966 | Common:1; Rare:49 | ||||
| chr12:13000212-13000430 | Common:1; Rare:76 | ||||
| chr12:13196534-13196849 | Common:1; Rare:56 | ||||
| chr12:14365482-14365719 | Common:1; Rare:77 | ||||
| chr12:14771109-14771220 | Rare:46 | ||||
| chr12:14774184-14774492 | Common:3; Rare:79 |