| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:131710678-131711164 | Common:2; Rare:566 | ||||
| chr12:131828142-131828542 | Common:16; Rare:335 | ||||
| chr12:131894300-131894762 | Common:7; Rare:335 | ||||
| chr12:131928952-131929352 | Common:60; Rare:555; Clinvar:6 | ||||
| chr12:131929320-131930599 | Common:8; Rare:825; Clinvar:11; Clinvar (benign):22 | ||||
| chr12:131949576-131950078 | Common:14; Rare:876 | ||||
| chr12:132083984-132084418 | Common:37; Rare:630 | ||||
| chr12:132084524-132085698 | Common:19; Rare:431 | ||||
| chr12:132143817-132144612 | Common:12; Rare:839 | ||||
| chr12:132489770-132490219 | Common:15; Rare:619 | ||||
| chr12:132506830-132507150 | Common:4; Rare:84 | ||||
| chr12:132559763-132560163 | Rare:273 | ||||
| chr12:132687255-132687689 | Common:17; Rare:834; Clinvar:60; Clinvar (benign):64; Clinvar (pathogenic):6 | ||||
| chr12:132687936-132688071 | Rare:29 | ||||
| chr12:132710340-132711050 | Common:35; Rare:1037 |