| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:183098799-183099553 | Common:8; Rare:339 | ||||
| chr4:183444010-183444370 | Common:4; Rare:225 | ||||
| chr4:183444469-183444787 | Common:3; Rare:252 | ||||
| chr4:183504050-183504840 | Common:9; Rare:322 | ||||
| chr4:183504860-183505100 | Common:2; Rare:133 | ||||
| chr4:183505980-183506116 | Rare:104 | ||||
| chr4:183659155-183659416 | Common:1; Rare:166 | ||||
| chr4:184474489-184474852 | Rare:161 | ||||
| chr4:184649392-184649843 | Common:9; Rare:275 | ||||
| chr4:184734052-184734460 | Common:16; Rare:275 | ||||
| chr4:184825936-184826173 | Common:10; Rare:149 | ||||
| chr4:185143112-185143306 | Common:3; Rare:102; Clinvar (benign):5 | ||||
| chr4:185203889-185204147 | Common:2; Rare:147 | ||||
| chr4:185209406-185209659 | Common:2; Rare:166 | ||||
| chr4:185396496-185396845 | Rare:205 |