| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:16077430-16077489 | Rare:19 | ||||
| chr19:16079373-16079575 | Common:1; Rare:39 | ||||
| chr19:16080118-16080238 | Rare:23 | ||||
| chr19:16111277-16111336 | Common:2; Rare:21 | ||||
| chr19:16111339-16111959 | Common:8; Rare:166 | ||||
| chr19:16143550-16143805 | Common:2; Rare:62 | ||||
| chr19:16185165-16185505 | Common:1; Rare:110 | ||||
| chr19:16197511-16197589 | Rare:14 | ||||
| chr19:16197644-16197995 | Common:4; Rare:110 | ||||
| chr19:16324658-16324904 | Rare:64 | ||||
| chr19:16471930-16472252 | Common:5; Rare:104 | ||||
| chr19:16496023-16496401 | Common:1; Rare:118; Clinvar:3; Clinvar (benign):1 | ||||
| chr19:16542332-16542713 | Common:2; Rare:128 | ||||
| chr19:16572291-16572699 | Common:5; Rare:153 | ||||
| chr19:16587057-16587220 | Common:2; Rare:34 |