| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:141876447-141876836 | Common:3; Rare:165 | ||||
| chr3:141915887-141915998 | Rare:24 | ||||
| chr3:142447974-142448288 | Common:3; Rare:93 | ||||
| chr3:142578697-142578927 | Rare:81; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:142596262-142596480 | Common:3; Rare:57 | ||||
| chr3:142723896-142724068 | Rare:50 | ||||
| chr3:142888883-142889061 | Common:3; Rare:52 | ||||
| chr3:142889072-142889233 | Rare:20 | ||||
| chr3:142963668-142963953 | Common:5; Rare:83 | ||||
| chr3:142963996-142964164 | Common:2; Rare:43 | ||||
| chr3:143001454-143001670 | Common:2; Rare:85 | ||||
| chr3:143002040-143002285 | Rare:63 | ||||
| chr3:143119606-143119837 | Rare:67 | ||||
| chr3:143971689-143971867 | Common:2; Rare:80 | ||||
| chr3:143971967-143972235 | Common:2; Rare:111 |