| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:63289215-63289364 | Rare:23 | ||||
| chr14:63290205-63290229 | Rare:5 | ||||
| chr14:63290507-63290987 | Common:7; Rare:85 | ||||
| chr14:63294464-63294783 | Common:1; Rare:60 | ||||
| chr14:63393818-63394056 | Rare:51 | ||||
| chr14:63722054-63722357 | Common:1; Rare:48 | ||||
| chr14:63883885-63883904 | Rare:3 | ||||
| chr14:63940091-63940335 | Common:1; Rare:57 | ||||
| chr14:63941761-63941914 | Common:1; Rare:29; Clinvar (benign):1 | ||||
| chr14:63944857-63945113 | Common:4; Rare:26 | ||||
| chr14:63988332-63988370 | Common:1; Rare:9 | ||||
| chr14:64219129-64219250 | Common:1; Rare:48 | ||||
| chr14:64365748-64365955 | Common:2; Rare:28 | ||||
| chr14:64416202-64416490 | Common:3; Rare:61 | ||||
| chr14:64441828-64442063 | Common:1; Rare:51 |