| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:611575-611975 | Common:4; Rare:61 | ||||
| chr5:612063-612463 | Rare:622 | ||||
| chr5:693223-693623 | Common:17; Rare:224 | ||||
| chr5:891056-891796 | Common:15; Rare:844 | ||||
| chr5:891774-892563 | Common:8; Rare:511 | ||||
| chr5:892495-893190 | Common:36; Rare:1021 | ||||
| chr5:1111182-1111582 | Common:2; Rare:100 | ||||
| chr5:1111835-1112313 | Common:3; Rare:320 | ||||
| chr5:1201029-1201525 | Common:21; Rare:368 | ||||
| chr5:1202060-1202310 | Rare:70 | ||||
| chr5:1294910-1295317 | Common:6; Rare:250; Clinvar:6; Clinvar (benign):7 | ||||
| chr5:1326211-1327156 | Common:41; Rare:231 | ||||
| chr5:1344171-1345320 | Common:20; Rare:1364 | ||||
| chr5:1523766-1524170 | Common:4; Rare:390 | ||||
| chr5:1524086-1524486 | Common:6; Rare:242 |