| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:69234714-69235114 | Common:7; Rare:449 | ||||
| chr5:69235167-69235567 | Common:4; Rare:134 | ||||
| chr5:69332540-69333060 | Common:1; Rare:321 | ||||
| chr5:69368622-69369094 | Common:5; Rare:198 | ||||
| chr5:69369040-69369361 | Common:28; Rare:316 | ||||
| chr5:69369370-69370310 | Common:16; Rare:1540 | ||||
| chr5:69559916-69560316 | Common:6; Rare:166 | ||||
| chr5:71455401-71456118 | Common:1; Rare:522; Clinvar (benign):1 | ||||
| chr5:71456067-71456322 | Common:1; Rare:62 | ||||
| chr5:71586490-71586978 | Common:7; Rare:277 | ||||
| chr5:71587030-71587415 | Common:9; Rare:453; Clinvar (benign):5 | ||||
| chr5:72106583-72106983 | Common:3; Rare:74 | ||||
| chr5:72106901-72108825 | Common:24; Rare:1525 | ||||
| chr5:72307504-72308270 | Common:14; Rare:323 | ||||
| chr5:72308240-72308714 | Common:9; Rare:372 |