| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:177600000-177600181 | Common:3; Rare:55; Clinvar (benign):2 | ||||
| chr5:177600368-177600468 | Common:1; Rare:19 | ||||
| chr5:178113280-178113690 | Common:5; Rare:129 | ||||
| chr5:178130300-178130720 | Common:2; Rare:99 | ||||
| chr5:178130837-178131063 | Common:1; Rare:63 | ||||
| chr5:178131365-178131650 | Common:3; Rare:59 | ||||
| chr5:178153857-178154116 | Rare:67; Clinvar:3; Clinvar (benign):1 | ||||
| chr5:178204243-178204628 | Common:6; Rare:157 | ||||
| chr5:178204880-178205635 | Common:8; Rare:354 | ||||
| chr5:178232380-178232539 | Common:6; Rare:87 | ||||
| chr5:178232752-178232929 | Common:2; Rare:74 | ||||
| chr5:178590250-178590560 | Common:3; Rare:72 | ||||
| chr5:178626410-178626810 | Common:4; Rare:107 | ||||
| chr5:178627039-178627281 | Common:7; Rare:87 | ||||
| chr5:178859740-178860137 | Common:4; Rare:109 |