| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:179624449-179624575 | Common:2; Rare:22 | ||||
| chr5:179698366-179698427 | Common:1; Rare:19 | ||||
| chr5:179698519-179699243 | Common:4; Rare:256 | ||||
| chr5:179806900-179807070 | Common:3; Rare:58 | ||||
| chr5:179820775-179820907 | Common:2; Rare:48; Clinvar (benign):1 | ||||
| chr5:179858798-179858965 | Rare:94 | ||||
| chr5:179907828-179908021 | Common:2; Rare:99 | ||||
| chr5:180072128-180072223 | Common:1; Rare:42 | ||||
| chr5:180809808-180809900 | Common:4; Rare:23 | ||||
| chr5:180810108-180810282 | Common:5; Rare:53 | ||||
| chr5:180861135-180861435 | Common:2; Rare:120 | ||||
| chr5:181223102-181223337 | Rare:87 | ||||
| chr5:181223628-181223750 | Common:3; Rare:30 | ||||
| chr5:181238098-181238348 | Common:1; Rare:55 | ||||
| chr5:181243680-181243960 | Common:4; Rare:101 |