| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:169620400-169620593 | Common:2; Rare:73 | ||||
| chr4:169660030-169660248 | Common:1; Rare:42 | ||||
| chr4:173370693-173371014 | Common:2; Rare:81 | ||||
| chr4:174283643-174283953 | Common:1; Rare:59 | ||||
| chr4:176319718-176320042 | Common:4; Rare:111 | ||||
| chr4:177442377-177442519 | Rare:85; Clinvar:2 | ||||
| chr4:183504522-183504633 | Rare:45 | ||||
| chr4:183659183-183659317 | Rare:35 | ||||
| chr4:184474454-184474852 | Rare:87 | ||||
| chr4:184649441-184649756 | Common:4; Rare:102 | ||||
| chr4:184825936-184826268 | Common:7; Rare:105 | ||||
| chr5:218141-218340 | Common:2; Rare:72; Clinvar:1; Clinvar (benign):2 | ||||
| chr5:443069-443286 | Common:10; Rare:101 | ||||
| chr5:612201-612358 | Rare:62 | ||||
| chr5:1799783-1799975 | Common:8; Rare:93 |