| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:99894357-99894615 | Common:3; Rare:90 | ||||
| chr4:99950223-99950476 | Rare:57 | ||||
| chr4:101347519-101347822 | Common:5; Rare:94 | ||||
| chr4:102760908-102761091 | Rare:66; Clinvar:1 | ||||
| chr4:102826796-102826980 | Rare:53 | ||||
| chr4:102827492-102827637 | Rare:50 | ||||
| chr4:102827708-102828160 | Common:4; Rare:146 | ||||
| chr4:102828168-102828299 | Common:2; Rare:39 | ||||
| chr4:102868814-102869063 | Common:2; Rare:81 | ||||
| chr4:103198315-103198559 | Common:2; Rare:66 | ||||
| chr4:104494883-104495197 | Common:3; Rare:66 | ||||
| chr4:105708645-105708849 | Common:1; Rare:67 | ||||
| chr4:106316169-106316625 | Common:5; Rare:146 | ||||
| chr4:107720181-107720516 | Common:7; Rare:134 | ||||
| chr4:107989710-107989925 | Common:5; Rare:104; Clinvar:4; Clinvar (benign):5 |