| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:24146579-24146881 | Common:1; Rare:94 | ||||
| chr14:24195400-24195744 | Common:2; Rare:76 | ||||
| chr14:24213065-24213188 | Rare:22 | ||||
| chr14:24213449-24213583 | Common:1; Rare:47 | ||||
| chr14:24232251-24232717 | Common:8; Rare:116 | ||||
| chr14:24232743-24232942 | Common:1; Rare:44 | ||||
| chr14:24242295-24242433 | Rare:46; Clinvar (benign):1 | ||||
| chr14:24242556-24242720 | Common:1; Rare:37; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:24271460-24271687 | Common:2; Rare:65 | ||||
| chr14:24299760-24299890 | Rare:44 | ||||
| chr14:24429861-24429980 | Rare:28 | ||||
| chr14:24442661-24443013 | Common:5; Rare:115 | ||||
| chr14:31025419-31025673 | Common:2; Rare:60 | ||||
| chr14:31207067-31207189 | Common:1; Rare:32 | ||||
| chr14:31207600-31207911 | Common:2; Rare:106 |