| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:110503842-110504264 | Common:4; Rare:142; Clinvar:1; Clinvar (benign):4 | ||||
| chr13:110559552-110559828 | Common:1; Rare:55 | ||||
| chr13:110901453-110901740 | Common:2; Rare:60 | ||||
| chr13:113351479-113351742 | Common:2; Rare:58 | ||||
| chr13:114065804-114065949 | Rare:34 | ||||
| chr13:114256985-114257113 | Rare:24 | ||||
| chr13:114268421-114268620 | Common:2; Rare:35 | ||||
| chr14:21082728-21082857 | Common:2; Rare:38 | ||||
| chr14:21085462-21085787 | Common:3; Rare:85 | ||||
| chr14:21736016-21736174 | Common:1; Rare:28 | ||||
| chr14:22147788-22148012 | Common:1; Rare:50 | ||||
| chr14:22303767-22304045 | Common:5; Rare:46 | ||||
| chr14:22422204-22422526 | Rare:59 | ||||
| chr14:22489428-22489467 | Rare:11 | ||||
| chr14:22531565-22531882 | Rare:57 |