| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:70839232-70839414 | Common:2; Rare:76 | ||||
| chr4:70839567-70839715 | Rare:48 | ||||
| chr4:70902158-70902435 | Common:5; Rare:96 | ||||
| chr4:70993427-70993808 | Common:6; Rare:122 | ||||
| chr4:71187170-71187333 | Common:1; Rare:55 | ||||
| chr4:72031933-72032148 | Common:2; Rare:83 | ||||
| chr4:72567931-72568081 | Rare:42 | ||||
| chr4:72569159-72569327 | Common:1; Rare:47 | ||||
| chr4:73069459-73069484 | Rare:12; Clinvar (benign):1 | ||||
| chr4:73069625-73069865 | Common:2; Rare:117 | ||||
| chr4:73258530-73258910 | Common:1; Rare:115 | ||||
| chr4:73259140-73259280 | Common:1; Rare:38 | ||||
| chr4:74157878-74158188 | Common:2; Rare:141 | ||||
| chr4:75514273-75514503 | Common:1; Rare:79 | ||||
| chr4:75630458-75630666 | Rare:47 |