| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:184475210-184475311 | Common:1; Rare:17 | ||||
| chr4:184529470-184529663 | Common:3; Rare:31 | ||||
| chr4:184530236-184530311 | Common:2; Rare:12 | ||||
| chr4:184537211-184537296 | Rare:14 | ||||
| chr4:184537436-184537754 | Common:4; Rare:78 | ||||
| chr4:184538024-184538112 | Rare:15 | ||||
| chr4:184538114-184538277 | Common:1; Rare:38 | ||||
| chr4:184650300-184650402 | Rare:20 | ||||
| chr4:184851077-184851364 | Common:2; Rare:51 | ||||
| chr4:185039471-185039751 | Common:3; Rare:41 | ||||
| chr4:185234896-185235049 | Common:2; Rare:17 | ||||
| chr4:185504442-185504608 | Common:1; Rare:62; Clinvar:4; Clinvar (benign):5 | ||||
| chr4:185573972-185574108 | Rare:20 | ||||
| chr4:186079475-186079565 | Rare:16 | ||||
| chr4:186190739-186190771 | Rare:7 |