| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:184734125-184734440 | Common:8; Rare:95 | ||||
| chr4:184805441-184805835 | Common:1; Rare:72 | ||||
| chr4:184808332-184808603 | Rare:51 | ||||
| chr4:184808666-184808768 | Rare:13 | ||||
| chr4:184825931-184826311 | Common:7; Rare:110 | ||||
| chr4:185143163-185143389 | Common:3; Rare:78; Clinvar:1; Clinvar (benign):5 | ||||
| chr4:185203891-185204095 | Rare:66 | ||||
| chr4:185209389-185209550 | Common:1; Rare:50 | ||||
| chr4:185395889-185396030 | Rare:44 | ||||
| chr4:185396556-185396885 | Rare:114 | ||||
| chr4:185425866-185426296 | Common:4; Rare:135 | ||||
| chr4:185471050-185471544 | Common:11; Rare:101 | ||||
| chr4:185535341-185535773 | Common:4; Rare:139; Clinvar:1; Clinvar (benign):9 | ||||
| chr4:185775197-185775540 | Common:4; Rare:58 | ||||
| chr4:185811685-185811955 | Common:1; Rare:55 |