| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:17810681-17811091 | Common:4; Rare:125 | ||||
| chr4:20252758-20252920 | Common:1; Rare:40 | ||||
| chr4:20700245-20700510 | Common:1; Rare:115 | ||||
| chr4:21544412-21544616 | Common:1; Rare:38 | ||||
| chr4:21697687-21697827 | Common:1; Rare:35 | ||||
| chr4:23889957-23890271 | Common:1; Rare:54 | ||||
| chr4:24584459-24584889 | Common:1; Rare:111 | ||||
| chr4:25160358-25160741 | Common:3; Rare:119; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25233847-25234071 | Rare:93 | ||||
| chr4:25376961-25377343 | Common:4; Rare:115 | ||||
| chr4:25914060-25914337 | Common:3; Rare:117 | ||||
| chr4:26320590-26320857 | Common:1; Rare:110 | ||||
| chr4:26320874-26321043 | Rare:58; Clinvar (benign):1 | ||||
| chr4:26583892-26584131 | Rare:51 | ||||
| chr4:26857464-26857739 | Common:4; Rare:78 |