| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:142578649-142579075 | Rare:390; Clinvar:3; Clinvar (benign):3 | ||||
| chr3:142595494-142595996 | Common:4; Rare:125 | ||||
| chr3:142596216-142596531 | Common:9; Rare:192 | ||||
| chr3:142723893-142724251 | Common:3; Rare:136 | ||||
| chr3:142724410-142724594 | Common:4; Rare:98 | ||||
| chr3:142724770-142725430 | Common:5; Rare:265 | ||||
| chr3:143001199-143001659 | Common:12; Rare:308 | ||||
| chr3:143971280-143971550 | Common:3; Rare:248 | ||||
| chr3:143971664-143972269 | Common:12; Rare:615 | ||||
| chr3:143972425-143972711 | Common:2; Rare:273 | ||||
| chr3:143972708-143972950 | Common:4; Rare:150 | ||||
| chr3:143973205-143973388 | Rare:121 | ||||
| chr3:143973651-143974051 | Common:1; Rare:123 | ||||
| chr3:146160806-146161247 | Common:5; Rare:286; Clinvar:9; Clinvar (benign):5 | ||||
| chr3:146161282-146161443 | Common:5; Rare:80; Clinvar:3; Clinvar (benign):2 |