| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:177524054-177524080 | Rare:11 | ||||
| chr5:177553265-177553501 | Rare:47 | ||||
| chr5:177592128-177592268 | Common:2; Rare:69 | ||||
| chr5:177592278-177592673 | Common:1; Rare:135; Clinvar:1 | ||||
| chr5:178153644-178153731 | Rare:37; Clinvar:5; Clinvar (benign):2 | ||||
| chr5:178204323-178204622 | Common:4; Rare:122 | ||||
| chr5:178205720-178205818 | Common:1; Rare:25 | ||||
| chr5:178231065-178231257 | Common:1; Rare:48 | ||||
| chr5:178232331-178232437 | Common:3; Rare:54 | ||||
| chr5:179550513-179550874 | Common:2; Rare:170 | ||||
| chr5:179559560-179559819 | Common:1; Rare:76 | ||||
| chr5:179618487-179618990 | Rare:111 | ||||
| chr5:179619971-179620107 | Rare:28 | ||||
| chr5:179621522-179621617 | Common:1; Rare:28 | ||||
| chr5:179624576-179624818 | Rare:45 |