| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:173168714-173168840 | Common:2; Rare:49 | ||||
| chr4:173334261-173334613 | Rare:96 | ||||
| chr4:173369765-173369935 | Common:1; Rare:55 | ||||
| chr4:173370690-173370986 | Common:2; Rare:76 | ||||
| chr4:173530160-173530514 | Common:3; Rare:70 | ||||
| chr4:174283601-174283948 | Common:1; Rare:69 | ||||
| chr4:176319742-176320096 | Common:4; Rare:117 | ||||
| chr4:177442371-177442521 | Rare:90; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr4:182917295-182917558 | Common:4; Rare:84 | ||||
| chr4:183658997-183659404 | Common:1; Rare:123 | ||||
| chr4:184474513-184474817 | Rare:67 | ||||
| chr4:184649420-184649805 | Common:4; Rare:124 | ||||
| chr4:184734125-184734426 | Common:6; Rare:89 | ||||
| chr4:185425866-185426267 | Common:4; Rare:124 | ||||
| chr4:186723783-186723911 | Common:4; Rare:51 |