| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:12576967-12577245 | Common:1; Rare:47 | ||||
| chr3:12584998-12585079 | Common:1; Rare:29; Clinvar (benign):1 | ||||
| chr3:12594233-12594530 | Rare:46 | ||||
| chr3:12643460-12643604 | Common:1; Rare:34 | ||||
| chr3:12838184-12838426 | Common:5; Rare:63 | ||||
| chr3:12838888-12838948 | Common:1; Rare:18 | ||||
| chr3:12839900-12840182 | Common:1; Rare:73 | ||||
| chr3:14125725-14125887 | Rare:40 | ||||
| chr3:14127842-14128130 | Common:1; Rare:55 | ||||
| chr3:14128990-14129225 | Common:2; Rare:42 | ||||
| chr3:14144455-14144763 | Common:5; Rare:77 | ||||
| chr3:14154335-14154625 | Common:2; Rare:53 | ||||
| chr3:14181328-14181618 | Common:1; Rare:56 | ||||
| chr3:14467884-14468202 | Rare:65 | ||||
| chr3:14664761-14665066 | Common:1; Rare:54 |