| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:196143300-196143740 | Common:7; Rare:134 | ||||
| chr3:196163590-196163990 | Common:6; Rare:83 | ||||
| chr3:196193771-196194200 | Common:4; Rare:136 | ||||
| chr3:196431176-196431410 | Common:2; Rare:41 | ||||
| chr3:196487249-196487800 | Rare:292; Clinvar (benign):4; Clinvar (pathogenic):4 | ||||
| chr3:196502620-196503080 | Common:1; Rare:215 | ||||
| chr3:196632070-196632540 | Common:13; Rare:206 | ||||
| chr3:196632610-196632732 | Rare:29 | ||||
| chr3:196740360-196740830 | Common:3; Rare:114 | ||||
| chr3:197478610-197479040 | Common:1; Rare:102 | ||||
| chr3:197487695-197488186 | Common:6; Rare:154 | ||||
| chr3:197554720-197555100 | Common:9; Rare:183 | ||||
| chr3:197627814-197628069 | Common:8; Rare:97 | ||||
| chr4:781767-782199 | Common:5; Rare:277 | ||||
| chr4:1777820-1778260 | Common:2; Rare:176 |