| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:68101494-68101737 | Common:6; Rare:97 | ||||
| chr17:68125698-68125973 | Common:4; Rare:49 | ||||
| chr17:76557449-76557854 | Common:3; Rare:106 | ||||
| chr17:77492712-77493057 | Common:2; Rare:78; Clinvar (benign):1 | ||||
| chr17:78908629-78908724 | Common:1; Rare:14 | ||||
| chr18:3593976-3594161 | Common:3; Rare:30 | ||||
| chr18:5238016-5238135 | Common:1; Rare:49 | ||||
| chr18:9359975-9360303 | Rare:67 | ||||
| chr18:11852341-11852577 | Common:2; Rare:65 | ||||
| chr18:12279145-12279452 | Common:1; Rare:66 | ||||
| chr18:76491475-76491628 | Common:2; Rare:71 | ||||
| chr19:1037585-1037665 | Common:1; Rare:32 | ||||
| chr19:1085556-1085810 | Common:1; Rare:148 | ||||
| chr19:2115219-2115612 | Common:4; Rare:144 | ||||
| chr19:3462572-3462770 | Common:2; Rare:48 |