| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:39458856-39459098 | Common:3; Rare:138; Clinvar (benign):4 | ||||
| chr4:39527520-39527746 | Common:2; Rare:59 | ||||
| chr4:39638863-39639209 | Common:1; Rare:135 | ||||
| chr4:39697889-39698188 | Common:2; Rare:122 | ||||
| chr4:40629666-40629933 | Common:1; Rare:68 | ||||
| chr4:40630304-40630546 | Common:1; Rare:50 | ||||
| chr4:47485151-47485320 | Common:1; Rare:54 | ||||
| chr4:48780254-48780288 | Rare:14 | ||||
| chr4:56387438-56387574 | Rare:50 | ||||
| chr4:56435586-56435765 | Common:1; Rare:60 | ||||
| chr4:56467569-56467709 | Common:2; Rare:58; Clinvar (benign):5 | ||||
| chr4:56977524-56977782 | Common:2; Rare:95 | ||||
| chr4:57110377-57110543 | Common:1; Rare:54 | ||||
| chr4:67701117-67701367 | Common:4; Rare:117 | ||||
| chr4:75514335-75514495 | Rare:48 |