| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:183905192-183905395 | Common:1; Rare:52 | ||||
| chr4:184474513-184474647 | Rare:25 | ||||
| chr4:184649406-184649892 | Common:4; Rare:148 | ||||
| chr4:184733342-184733538 | Common:4; Rare:54 | ||||
| chr4:184734014-184734459 | Common:11; Rare:180 | ||||
| chr4:185143136-185143322 | Common:2; Rare:63; Clinvar (benign):3 | ||||
| chr4:185203906-185204097 | Rare:64 | ||||
| chr4:185396563-185396708 | Rare:51 | ||||
| chr4:185425870-185426019 | Common:2; Rare:56 | ||||
| chr4:185535363-185535632 | Common:2; Rare:99; Clinvar:1; Clinvar (benign):9 | ||||
| chr4:186191494-186191814 | Common:5; Rare:107; Clinvar:2; Clinvar (benign):5 | ||||
| chr4:186723759-186723910 | Common:4; Rare:64 | ||||
| chr4:189940574-189941037 | Common:18; Rare:156 | ||||
| chr5:218112-218378 | Common:3; Rare:114; Clinvar:8; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr5:443084-443269 | Common:10; Rare:84 |