| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:173168506-173168813 | Common:2; Rare:82 | ||||
| chr4:173370688-173371009 | Common:2; Rare:82 | ||||
| chr4:174283631-174283967 | Common:1; Rare:65 | ||||
| chr4:176319721-176320055 | Common:4; Rare:115 | ||||
| chr4:177442384-177442519 | Rare:79; Clinvar:2 | ||||
| chr4:183444438-183444812 | Common:2; Rare:171 | ||||
| chr4:183504401-183504641 | Rare:87 | ||||
| chr4:183505231-183505346 | Common:1; Rare:29 | ||||
| chr4:183659166-183659337 | Rare:51 | ||||
| chr4:184474484-184474808 | Rare:71 | ||||
| chr4:184649397-184649770 | Common:5; Rare:125 | ||||
| chr4:184734029-184734430 | Common:8; Rare:158 | ||||
| chr4:185143094-185143299 | Common:3; Rare:66; Clinvar (benign):3 | ||||
| chr4:185203897-185204097 | Rare:66 | ||||
| chr4:185396438-185396815 | Rare:126 |