| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:40629813-40629976 | Common:1; Rare:39 | ||||
| chr4:41214458-41214788 | Common:5; Rare:77 | ||||
| chr4:41360680-41360785 | Rare:25 | ||||
| chr4:41990406-41990566 | Common:1; Rare:60 | ||||
| chr4:44678265-44678492 | Common:2; Rare:74 | ||||
| chr4:47485166-47485340 | Common:1; Rare:62 | ||||
| chr4:47914593-47914898 | Common:1; Rare:85 | ||||
| chr4:48016618-48016784 | Common:1; Rare:48 | ||||
| chr4:48269795-48269971 | Common:2; Rare:37 | ||||
| chr4:48341214-48341478 | Common:1; Rare:111 | ||||
| chr4:48780245-48780572 | Common:2; Rare:97 | ||||
| chr4:52038255-52038412 | Rare:56; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr4:52659234-52659398 | Common:1; Rare:58 | ||||
| chr4:55546805-55546862 | Rare:12 | ||||
| chr4:55546865-55546998 | Common:2; Rare:53 |