| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:68715024-68715229 | Common:2; Rare:89 | ||||
| chr18:70205659-70205774 | Common:3; Rare:48; Clinvar (benign):2 | ||||
| chr18:74148349-74148599 | Common:1; Rare:77 | ||||
| chr18:74496046-74496389 | Common:4; Rare:107 | ||||
| chr18:74499822-74499881 | Rare:16 | ||||
| chr18:74597611-74597907 | Common:2; Rare:76 | ||||
| chr19:344790-344951 | Common:3; Rare:59 | ||||
| chr19:572295-572618 | Common:1; Rare:161 | ||||
| chr19:633520-633715 | Common:8; Rare:90 | ||||
| chr19:663132-663426 | Common:2; Rare:113 | ||||
| chr19:893177-893480 | Common:3; Rare:127 | ||||
| chr19:913164-913296 | Rare:42 | ||||
| chr19:984225-984348 | Common:1; Rare:46 | ||||
| chr19:1039924-1040160 | Common:2; Rare:71 | ||||
| chr19:1067099-1067187 | Common:1; Rare:25 |