| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:40403533-40403755 | Common:1; Rare:70; Clinvar:1 | ||||
| chr19:40404240-40404449 | Common:1; Rare:44 | ||||
| chr19:40411601-40411849 | Common:2; Rare:32 | ||||
| chr19:40417150-40417341 | Common:1; Rare:50 | ||||
| chr19:40420950-40421471 | Common:4; Rare:105 | ||||
| chr19:40424475-40425146 | Common:2; Rare:131 | ||||
| chr19:40433466-40433575 | Common:1; Rare:23 | ||||
| chr19:40433902-40434195 | Common:2; Rare:77 | ||||
| chr19:40443282-40443444 | Common:4; Rare:47 | ||||
| chr19:40463287-40463420 | Common:3; Rare:20 | ||||
| chr19:40523388-40523540 | Common:1; Rare:42 | ||||
| chr19:40549270-40549590 | Rare:82 | ||||
| chr19:40604015-40604231 | Rare:42 | ||||
| chr19:40605621-40605749 | Rare:39; Clinvar:2; Clinvar (benign):1 | ||||
| chr19:40634560-40634830 | Common:3; Rare:43 |