| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:19192110-19192255 | Common:1; Rare:44 | ||||
| chr19:19192563-19193015 | Common:3; Rare:114; Clinvar (benign):1 | ||||
| chr19:19320472-19320870 | Common:4; Rare:149 | ||||
| chr19:19516126-19516302 | Rare:116; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr19:19668511-19668843 | Rare:88 | ||||
| chr19:19821668-19821907 | Common:1; Rare:80 | ||||
| chr19:20077818-20077992 | Common:2; Rare:49 | ||||
| chr19:20565746-20565932 | Rare:51 | ||||
| chr19:20661525-20661753 | Common:7; Rare:64 | ||||
| chr19:21141886-21142096 | Rare:59 | ||||
| chr19:21836112-21836331 | Rare:84 | ||||
| chr19:23687144-23687343 | Common:3; Rare:50 | ||||
| chr19:29213114-29213259 | Common:2; Rare:49 | ||||
| chr19:29606163-29606324 | Rare:53 | ||||
| chr19:29665252-29665532 | Common:4; Rare:101 |