| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:172959373-172959515 | Common:1; Rare:48 | ||||
| chr5:173328400-173328596 | Rare:38 | ||||
| chr5:176388550-176388811 | Common:4; Rare:103 | ||||
| chr5:176448216-176448402 | Common:1; Rare:69 | ||||
| chr5:177022634-177022741 | Rare:39 | ||||
| chr5:177133488-177133794 | Rare:111 | ||||
| chr5:177303691-177304029 | Common:3; Rare:135 | ||||
| chr5:177351643-177351716 | Rare:20 | ||||
| chr5:177497552-177497868 | Common:1; Rare:116 | ||||
| chr5:177516872-177517066 | Common:2; Rare:81; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr5:179559504-179559805 | Common:1; Rare:95 | ||||
| chr5:179806886-179807063 | Common:3; Rare:67 | ||||
| chr5:179858798-179858993 | Rare:108 | ||||
| chr5:180353321-180353513 | Common:5; Rare:79 | ||||
| chr5:181261081-181261262 | Rare:61 |