| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:99950266-99950477 | Rare:40 | ||||
| chr4:100517919-100518128 | Rare:48 | ||||
| chr4:101347517-101347816 | Common:5; Rare:94 | ||||
| chr4:102345473-102345596 | Rare:31 | ||||
| chr4:102501505-102501705 | Rare:64 | ||||
| chr4:102827462-102828138 | Common:4; Rare:224 | ||||
| chr4:102868850-102869087 | Common:2; Rare:84 | ||||
| chr4:103019653-103019960 | Common:3; Rare:68 | ||||
| chr4:104494888-104495192 | Common:3; Rare:63 | ||||
| chr4:105146594-105146898 | Common:1; Rare:98 | ||||
| chr4:105552342-105552645 | Rare:44 | ||||
| chr4:105708641-105708856 | Common:2; Rare:71 | ||||
| chr4:106316063-106316607 | Common:5; Rare:171 | ||||
| chr4:107989679-107989941 | Common:6; Rare:117; Clinvar:4; Clinvar (benign):5 | ||||
| chr4:108620393-108620640 | Common:6; Rare:123 |