| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:183659083-183659439 | Common:1; Rare:113 | ||||
| chr4:184474438-184474816 | Common:1; Rare:79 | ||||
| chr4:184649406-184649796 | Common:4; Rare:126 | ||||
| chr4:184805512-184805922 | Common:2; Rare:70 | ||||
| chr4:185143163-185143322 | Common:2; Rare:58; Clinvar (benign):3 | ||||
| chr4:185396563-185396851 | Rare:93 | ||||
| chr4:185425873-185426217 | Common:3; Rare:99 | ||||
| chr4:185471070-185471412 | Common:10; Rare:40 | ||||
| chr4:185535359-185535668 | Common:2; Rare:113; Clinvar:1; Clinvar (benign):9 | ||||
| chr4:185657299-185657356 | Common:1; Rare:12 | ||||
| chr4:186191459-186191826 | Common:6; Rare:124; Clinvar:2; Clinvar (benign):5 | ||||
| chr4:186723759-186723917 | Common:5; Rare:65 | ||||
| chr4:186726544-186726932 | Common:4; Rare:119 | ||||
| chr4:189940588-189941035 | Common:18; Rare:153 | ||||
| chr5:218114-218415 | Common:3; Rare:121; Clinvar:11; Clinvar (benign):10; Clinvar (pathogenic):2 |