| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45768384-45768579 | Rare:65; Clinvar:1 | ||||
| chr19:45768703-45768871 | Rare:60; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:45768982-45769095 | Common:2; Rare:42 | ||||
| chr19:45769183-45769714 | Common:3; Rare:215 | ||||
| chr19:45770503-45771027 | Common:4; Rare:237; Clinvar:3 | ||||
| chr19:45779573-45779826 | Common:1; Rare:71 | ||||
| chr19:45792326-45792388 | Rare:14 | ||||
| chr19:45792715-45793143 | Common:7; Rare:120 | ||||
| chr19:45862411-45862743 | Common:3; Rare:78 | ||||
| chr19:45863032-45863433 | Common:5; Rare:123 | ||||
| chr19:45864136-45864381 | Common:2; Rare:56 | ||||
| chr19:45885821-45886028 | Rare:37 | ||||
| chr19:45886039-45886231 | Common:1; Rare:75 | ||||
| chr19:45886427-45886600 | Common:3; Rare:28 | ||||
| chr19:45902565-45902956 | Common:3; Rare:122 |