| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:52659166-52659439 | Common:1; Rare:91 | ||||
| chr4:52862175-52862322 | Common:5; Rare:65 | ||||
| chr4:54229171-54229414 | Common:1; Rare:40; Clinvar (benign):2 | ||||
| chr4:55948757-55948899 | Rare:27 | ||||
| chr4:56387397-56387568 | Rare:61 | ||||
| chr4:56435478-56435770 | Common:5; Rare:106 | ||||
| chr4:56436042-56436324 | Rare:103 | ||||
| chr4:56467532-56467721 | Common:2; Rare:78; Clinvar (benign):5 | ||||
| chr4:56977513-56977780 | Common:2; Rare:97 | ||||
| chr4:57110330-57110584 | Common:2; Rare:75 | ||||
| chr4:67701057-67701431 | Common:4; Rare:170 | ||||
| chr4:70688477-70688816 | Common:4; Rare:88 | ||||
| chr4:70839201-70839419 | Common:2; Rare:87 | ||||
| chr4:70902229-70902423 | Common:3; Rare:65 | ||||
| chr4:73258772-73258910 | Rare:39 |