| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:138018884-138019027 | Rare:34 | ||||
| chr5:138567584-138567722 | Rare:36 | ||||
| chr5:138947441-138947698 | Common:1; Rare:59; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr5:139280111-139280411 | Common:2; Rare:52 | ||||
| chr5:139325412-139325923 | Rare:149; Clinvar:6; Clinvar (benign):3 | ||||
| chr5:140537953-140538262 | Rare:65 | ||||
| chr5:140556249-140556468 | Rare:37 | ||||
| chr5:140565622-140565966 | Common:3; Rare:55 | ||||
| chr5:140645622-140645882 | Rare:57; Clinvar (benign):2 | ||||
| chr5:140661699-140661937 | Common:2; Rare:40 | ||||
| chr5:140689193-140689457 | Common:3; Rare:43 | ||||
| chr5:140718826-140718925 | Common:3; Rare:36 | ||||
| chr5:141318461-141318496 | Rare:6 | ||||
| chr5:141318748-141319255 | Common:1; Rare:113 | ||||
| chr5:141418308-141418535 | Rare:66 |