| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:56435980-56436315 | Rare:117 | ||||
| chr4:56467542-56467699 | Common:2; Rare:66; Clinvar (benign):5 | ||||
| chr4:56977521-56977751 | Common:2; Rare:86 | ||||
| chr4:67545423-67545742 | Common:2; Rare:80 | ||||
| chr4:67701061-67701391 | Common:4; Rare:152 | ||||
| chr4:68349952-68350200 | Rare:90 | ||||
| chr4:70688297-70688586 | Common:2; Rare:72 | ||||
| chr4:70688928-70689211 | Common:1; Rare:102 | ||||
| chr4:70993416-70993722 | Common:5; Rare:98 | ||||
| chr4:73069707-73069875 | Common:1; Rare:73 | ||||
| chr4:73258460-73258887 | Common:1; Rare:119 | ||||
| chr4:73259124-73259180 | Rare:10 | ||||
| chr4:73998416-73998498 | Rare:37 | ||||
| chr4:73998568-73998748 | Rare:49 | ||||
| chr4:74038687-74038867 | Rare:50 |