| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:142578700-142578927 | Rare:80; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:142596427-142596451 | Rare:7 | ||||
| chr3:142723884-142724042 | Rare:45 | ||||
| chr3:143001472-143001632 | Common:2; Rare:57 | ||||
| chr3:143119601-143119796 | Rare:51 | ||||
| chr3:143971867-143972075 | Common:1; Rare:72 | ||||
| chr3:146160975-146161327 | Common:2; Rare:114; Clinvar:5; Clinvar (benign):2 | ||||
| chr3:146544484-146544945 | Common:5; Rare:113 | ||||
| chr3:147406511-147406731 | Rare:40 | ||||
| chr3:147409129-147409496 | Rare:102 | ||||
| chr3:147421233-147421396 | Common:2; Rare:46 | ||||
| chr3:149086424-149086722 | Rare:90 | ||||
| chr3:149129549-149129721 | Common:1; Rare:72; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:149377628-149377863 | Common:1; Rare:54 | ||||
| chr3:149752408-149752540 | Common:2; Rare:51 |