| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:102809670-102809851 | Common:1; Rare:40 | ||||
| chr4:102827110-102827428 | Common:1; Rare:117 | ||||
| chr4:102827433-102827941 | Common:4; Rare:171 | ||||
| chr4:102827947-102828286 | Common:2; Rare:115 | ||||
| chr4:102868813-102869083 | Common:2; Rare:92 | ||||
| chr4:103076198-103076402 | Rare:63 | ||||
| chr4:105708628-105708847 | Common:1; Rare:71 | ||||
| chr4:106316161-106316625 | Common:5; Rare:150 | ||||
| chr4:107720193-107720562 | Common:7; Rare:150 | ||||
| chr4:107824305-107824693 | Common:1; Rare:76 | ||||
| chr4:107824769-107825055 | Common:1; Rare:86 | ||||
| chr4:107989646-107990029 | Common:6; Rare:163; Clinvar:5; Clinvar (benign):5 | ||||
| chr4:108620384-108620647 | Common:6; Rare:134 | ||||
| chr4:108762842-108763212 | Common:1; Rare:106 | ||||
| chr4:109433757-109433926 | Common:1; Rare:58 |