| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:36053986-36054627 | Common:3; Rare:205 | ||||
| chr19:36054708-36054997 | Common:1; Rare:102; Clinvar:2; Clinvar (benign):1 | ||||
| chr19:36055189-36055537 | Common:2; Rare:63 | ||||
| chr19:36114214-36114566 | Common:1; Rare:111 | ||||
| chr19:36114799-36115006 | Common:2; Rare:85 | ||||
| chr19:36115147-36115597 | Common:4; Rare:142 | ||||
| chr19:36115654-36115868 | Rare:52 | ||||
| chr19:36139481-36139592 | Common:1; Rare:25 | ||||
| chr19:36139621-36139739 | Common:1; Rare:17 | ||||
| chr19:36139815-36140162 | Common:1; Rare:102 | ||||
| chr19:36140485-36140681 | Rare:31 | ||||
| chr19:36140874-36141008 | Rare:30 | ||||
| chr19:36141026-36141039 | Rare:2 | ||||
| chr19:36141101-36141346 | Common:5; Rare:119 | ||||
| chr19:36214489-36214773 | Common:2; Rare:93 |