| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:183504940-183505126 | Common:1; Rare:53 | ||||
| chr4:183659090-183659401 | Common:1; Rare:103 | ||||
| chr4:184474438-184474829 | Common:1; Rare:86 | ||||
| chr4:184649410-184649794 | Common:4; Rare:124 | ||||
| chr4:185395921-185396056 | Rare:44 | ||||
| chr4:185396563-185396694 | Rare:44 | ||||
| chr4:185425870-185426014 | Common:2; Rare:55 | ||||
| chr4:185471051-185471533 | Common:11; Rare:96 | ||||
| chr4:185535341-185535630 | Common:2; Rare:106; Clinvar:1; Clinvar (benign):9 | ||||
| chr4:185657181-185657374 | Common:1; Rare:41 | ||||
| chr4:185657386-185657434 | Rare:16 | ||||
| chr4:186191505-186191826 | Common:5; Rare:108; Clinvar:2; Clinvar (benign):5 | ||||
| chr4:186723759-186723953 | Common:5; Rare:78 | ||||
| chr4:189940605-189941046 | Common:18; Rare:158 | ||||
| chr5:218107-218409 | Common:4; Rare:120; Clinvar:11; Clinvar (benign):9; Clinvar (pathogenic):2 |