| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:16542429-16542593 | Common:2; Rare:41 | ||||
| chr19:16660112-16660386 | Common:3; Rare:100 | ||||
| chr19:17215625-17215760 | Common:1; Rare:36 | ||||
| chr19:17305687-17305893 | Common:1; Rare:89 | ||||
| chr19:17337327-17337584 | Common:1; Rare:58 | ||||
| chr19:18152934-18153262 | Common:1; Rare:102 | ||||
| chr19:18323018-18323281 | Common:3; Rare:90 | ||||
| chr19:18683440-18683691 | Common:2; Rare:71 | ||||
| chr19:18919335-18919705 | Common:2; Rare:122 | ||||
| chr19:19033482-19033882 | Common:2; Rare:110 | ||||
| chr19:19192122-19192212 | Common:1; Rare:31 | ||||
| chr19:19192574-19192990 | Common:2; Rare:108 | ||||
| chr19:19516163-19516321 | Rare:96; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr19:19821710-19821873 | Common:1; Rare:52 | ||||
| chr19:23395443-23395672 | Common:1; Rare:56 |