| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:16898392-16898723 | Rare:72 | ||||
| chr4:17512054-17512280 | Common:3; Rare:85; Clinvar:2; Clinvar (benign):3 | ||||
| chr4:17614548-17614660 | Common:2; Rare:49 | ||||
| chr4:17810677-17811061 | Common:4; Rare:123 | ||||
| chr4:18021649-18022025 | Common:2; Rare:166 | ||||
| chr4:23889904-23890278 | Common:1; Rare:65 | ||||
| chr4:24584381-24584718 | Common:1; Rare:104 | ||||
| chr4:24795348-24795592 | Common:1; Rare:61 | ||||
| chr4:25160358-25160727 | Common:3; Rare:113; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25233841-25234078 | Rare:99 | ||||
| chr4:25376966-25377344 | Common:4; Rare:113 | ||||
| chr4:25914051-25914326 | Common:2; Rare:117 | ||||
| chr4:26163440-26163530 | Common:2; Rare:12 | ||||
| chr4:26319650-26319830 | Rare:50 | ||||
| chr4:26320590-26320832 | Common:1; Rare:92 |