| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:1720538-1720612 | Rare:17 | ||||
| chr4:1721241-1721524 | Common:2; Rare:86 | ||||
| chr4:2041875-2042017 | Common:1; Rare:54 | ||||
| chr4:2242042-2242423 | Common:1; Rare:139 | ||||
| chr4:2418674-2419006 | Common:5; Rare:104 | ||||
| chr4:2468871-2469187 | Common:4; Rare:122 | ||||
| chr4:2843699-2844022 | Common:3; Rare:117 | ||||
| chr4:2867719-2867972 | Rare:39 | ||||
| chr4:2934767-2934938 | Common:4; Rare:77 | ||||
| chr4:2963309-2963620 | Common:3; Rare:119 | ||||
| chr4:3074516-3074708 | Common:4; Rare:64 | ||||
| chr4:3292734-3293079 | Common:3; Rare:132 | ||||
| chr4:3385564-3385721 | Rare:31 | ||||
| chr4:3532222-3532385 | Rare:75; Clinvar (pathogenic):1 | ||||
| chr4:4248194-4248293 | Common:2; Rare:41 |