| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:183505980-183506116 | Rare:53 | ||||
| chr4:183659105-183659411 | Common:1; Rare:102 | ||||
| chr4:184474039-184474129 | Common:1; Rare:21 | ||||
| chr4:184474461-184474860 | Rare:88 | ||||
| chr4:184649427-184649796 | Common:4; Rare:117 | ||||
| chr4:184805475-184805832 | Common:1; Rare:67 | ||||
| chr4:184825917-184826288 | Common:7; Rare:109 | ||||
| chr4:185203904-185204167 | Common:2; Rare:87 | ||||
| chr4:185395831-185396080 | Common:2; Rare:72 | ||||
| chr4:185396581-185396845 | Rare:85 | ||||
| chr4:185425864-185426265 | Common:4; Rare:126 | ||||
| chr4:185535352-185535632 | Common:2; Rare:102; Clinvar:1; Clinvar (benign):9 | ||||
| chr4:186191543-186191870 | Common:5; Rare:106; Clinvar:2; Clinvar (benign):4 | ||||
| chr4:186723754-186723879 | Common:4; Rare:55 | ||||
| chr4:189940605-189941042 | Common:18; Rare:155 |