| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:176388236-176388973 | Common:5; Rare:255 | ||||
| chr5:176388978-176389217 | Common:1; Rare:70 | ||||
| chr5:176448045-176448410 | Common:1; Rare:116 | ||||
| chr5:177022569-177022908 | Common:1; Rare:121 | ||||
| chr5:177303645-177303988 | Common:4; Rare:141 | ||||
| chr5:177351585-177351731 | Rare:53 | ||||
| chr5:177367211-177367374 | Common:1; Rare:32 | ||||
| chr5:177446787-177446887 | Rare:34 | ||||
| chr5:177447868-177448066 | Common:2; Rare:40 | ||||
| chr5:177460435-177460705 | Common:1; Rare:90 | ||||
| chr5:177473551-177473747 | Common:1; Rare:72 | ||||
| chr5:177484491-177484778 | Common:2; Rare:51 | ||||
| chr5:177492388-177492671 | Common:1; Rare:113 | ||||
| chr5:177512096-177512340 | Common:1; Rare:69; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:177516789-177517073 | Common:2; Rare:119; Clinvar:1; Clinvar (pathogenic):1 |