| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:55948610-55949440 | Common:4; Rare:189 | ||||
| chr4:56048948-56049151 | Common:2; Rare:59 | ||||
| chr4:56387078-56387273 | Rare:39 | ||||
| chr4:56387326-56387652 | Rare:111 | ||||
| chr4:56435256-56435379 | Rare:44 | ||||
| chr4:56435448-56435827 | Common:5; Rare:125 | ||||
| chr4:56435961-56436373 | Rare:151 | ||||
| chr4:56467481-56467697 | Common:2; Rare:91; Clinvar (benign):5 | ||||
| chr4:56467889-56467981 | Common:2; Rare:26 | ||||
| chr4:56907746-56908045 | Common:4; Rare:100 | ||||
| chr4:56908517-56908777 | Common:2; Rare:62 | ||||
| chr4:56908844-56908928 | Common:1; Rare:25 | ||||
| chr4:56909206-56909354 | Rare:32 | ||||
| chr4:56977485-56977851 | Common:2; Rare:126 | ||||
| chr4:56977923-56978097 | Rare:29 |