| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:55346137-55346332 | Common:3; Rare:68; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:55395858-55395957 | Rare:27; Clinvar:2 | ||||
| chr4:55546808-55547020 | Common:2; Rare:73 | ||||
| chr4:56387423-56387543 | Rare:41 | ||||
| chr4:56435473-56435973 | Common:6; Rare:164 | ||||
| chr4:56435994-56436307 | Rare:111 | ||||
| chr4:56467507-56467708 | Common:2; Rare:82; Clinvar (benign):5 | ||||
| chr4:56656301-56656596 | Common:3; Rare:51 | ||||
| chr4:56681028-56681381 | Rare:60 | ||||
| chr4:56681520-56681755 | Common:1; Rare:27 | ||||
| chr4:56977589-56977732 | Common:1; Rare:53 | ||||
| chr4:61201340-61201374 | Rare:9 | ||||
| chr4:65670408-65670636 | Common:1; Rare:55 | ||||
| chr4:67545423-67545714 | Common:2; Rare:71 | ||||
| chr4:67701111-67701358 | Common:4; Rare:118 |