| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:182917325-182917619 | Common:4; Rare:93 | ||||
| chr4:183504522-183504809 | Common:2; Rare:94 | ||||
| chr4:183506009-183506110 | Rare:41 | ||||
| chr4:183659096-183659426 | Common:1; Rare:108 | ||||
| chr4:183960144-183960310 | Common:2; Rare:30 | ||||
| chr4:184474497-184474823 | Rare:76 | ||||
| chr4:184649396-184649796 | Common:5; Rare:130 | ||||
| chr4:184734044-184734403 | Common:5; Rare:134 | ||||
| chr4:185143041-185143353 | Common:5; Rare:98; Clinvar:1; Clinvar (benign):4 | ||||
| chr4:185203882-185204251 | Common:3; Rare:119 | ||||
| chr4:185210648-185210831 | Common:2; Rare:27 | ||||
| chr4:185395840-185396017 | Common:2; Rare:49 | ||||
| chr4:185396563-185396858 | Rare:96 | ||||
| chr4:185425878-185426289 | Common:4; Rare:123 | ||||
| chr4:185471049-185471428 | Common:10; Rare:52 |