| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:102827433-102827902 | Common:4; Rare:157 | ||||
| chr4:102827904-102828288 | Common:3; Rare:129 | ||||
| chr4:102868844-102869068 | Common:2; Rare:80 | ||||
| chr4:103076303-103076372 | Rare:22 | ||||
| chr4:105708628-105708827 | Rare:63 | ||||
| chr4:106316161-106316635 | Common:5; Rare:156 | ||||
| chr4:107720201-107720504 | Common:7; Rare:117 | ||||
| chr4:107824778-107825044 | Common:1; Rare:78 | ||||
| chr4:107989679-107990059 | Common:6; Rare:160; Clinvar:5; Clinvar (benign):5 | ||||
| chr4:108620384-108620609 | Common:6; Rare:113 | ||||
| chr4:108762994-108763202 | Common:1; Rare:41 | ||||
| chr4:109730044-109730280 | Common:2; Rare:56 | ||||
| chr4:109815493-109815786 | Common:1; Rare:79 | ||||
| chr4:110476015-110476286 | Common:1; Rare:56 | ||||
| chr4:112145293-112145475 | Common:1; Rare:47 |