| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:36772795-36773103 | Common:3; Rare:80 | ||||
| chr19:36850770-36850916 | Rare:36 | ||||
| chr19:36915996-36916371 | Common:3; Rare:66 | ||||
| chr19:37078181-37078473 | Common:3; Rare:69 | ||||
| chr19:37218120-37218240 | Rare:24 | ||||
| chr19:37317635-37317911 | Common:6; Rare:75 | ||||
| chr19:37467183-37467529 | Common:2; Rare:98 | ||||
| chr19:37507011-37507168 | Common:2; Rare:47 | ||||
| chr19:37594739-37594886 | Rare:42 | ||||
| chr19:37779594-37779662 | Rare:11 | ||||
| chr19:38264843-38264873 | Rare:15 | ||||
| chr19:38647372-38647713 | Common:3; Rare:120 | ||||
| chr19:38899572-38899959 | Rare:106 | ||||
| chr19:38930737-38930987 | Common:2; Rare:68; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:39391057-39391418 | Common:1; Rare:149 |