| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:114162849-114162933 | Rare:22 | ||||
| chr11:114167929-114168198 | Common:1; Rare:49 | ||||
| chr11:114178836-114179135 | Common:3; Rare:46 | ||||
| chr11:114179195-114179234 | Rare:7 | ||||
| chr11:120133569-120133723 | Rare:29 | ||||
| chr11:120135982-120136071 | Common:1; Rare:16 | ||||
| chr11:120137025-120137174 | Rare:26 | ||||
| chr11:129642055-129642135 | Common:1; Rare:16 | ||||
| chr12:16737-16850 | Common:5; Rare:37 | ||||
| chr12:753794-754098 | Common:2; Rare:109; Clinvar:7; Clinvar (benign):4 | ||||
| chr12:1581850-1582126 | Rare:44 | ||||
| chr12:2799613-2799880 | Rare:50 | ||||
| chr12:6233111-6233486 | Common:1; Rare:82 | ||||
| chr12:6233846-6233945 | Common:1; Rare:16 | ||||
| chr12:6372725-6372961 | Common:5; Rare:34 |