| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:98929080-98929382 | Common:3; Rare:79 | ||||
| chr4:99088702-99088884 | Common:6; Rare:79 | ||||
| chr4:99894357-99894597 | Common:2; Rare:88 | ||||
| chr4:99950248-99950527 | Rare:60 | ||||
| chr4:100190458-100190584 | Common:2; Rare:29 | ||||
| chr4:102826761-102826986 | Rare:64 | ||||
| chr4:102827481-102827849 | Common:4; Rare:122 | ||||
| chr4:102827985-102828299 | Common:3; Rare:106 | ||||
| chr4:102868844-102869063 | Common:2; Rare:75 | ||||
| chr4:105708649-105708843 | Common:1; Rare:62 | ||||
| chr4:106316199-106316612 | Common:5; Rare:133 | ||||
| chr4:107720175-107720493 | Common:7; Rare:128 | ||||
| chr4:107989690-107989900 | Common:5; Rare:100; Clinvar:4; Clinvar (benign):5 | ||||
| chr4:108620408-108620711 | Common:6; Rare:139 | ||||
| chr4:109433783-109433920 | Common:1; Rare:45 |