| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:62186937-62187305 | Common:5; Rare:102 | ||||
| chr18:68714988-68715284 | Common:6; Rare:126 | ||||
| chr18:70205672-70205856 | Common:3; Rare:71; Clinvar (benign):2 | ||||
| chr18:74291911-74292206 | Common:2; Rare:80 | ||||
| chr19:572331-572600 | Rare:136 | ||||
| chr19:633505-633747 | Common:8; Rare:112 | ||||
| chr19:663146-663486 | Common:3; Rare:138 | ||||
| chr19:680469-680754 | Common:2; Rare:98 | ||||
| chr19:893158-893553 | Common:3; Rare:211 | ||||
| chr19:1026494-1026683 | Rare:74 | ||||
| chr19:1103768-1104118 | Common:6; Rare:149 | ||||
| chr19:1269036-1269341 | Common:3; Rare:113 | ||||
| chr19:1275788-1276113 | Common:2; Rare:144 | ||||
| chr19:2096235-2096397 | Rare:55 | ||||
| chr19:2269503-2269677 | Common:2; Rare:78 |