| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49662671-49663071 | Common:2; Rare:68 | ||||
| chr19:49664348-49664754 | Common:7; Rare:566 | ||||
| chr19:49665215-49665615 | Common:1; Rare:167 | ||||
| chr19:49665569-49666481 | Common:30; Rare:1332; Clinvar (pathogenic):7 | ||||
| chr19:49672006-49672406 | Common:1; Rare:105 | ||||
| chr19:49675297-49676392 | Common:7; Rare:362 | ||||
| chr19:49676297-49677305 | Common:24; Rare:846 | ||||
| chr19:49677280-49677530 | Rare:121 | ||||
| chr19:49677500-49678146 | Common:1; Rare:340 | ||||
| chr19:49678340-49678790 | Common:2; Rare:119 | ||||
| chr19:49683583-49685068 | Common:16; Rare:621 | ||||
| chr19:49712200-49712720 | Common:15; Rare:469 | ||||
| chr19:49766220-49767018 | Common:7; Rare:700 | ||||
| chr19:49766972-49767446 | Common:1; Rare:220 | ||||
| chr19:49808693-49809380 | Common:14; Rare:596; Clinvar:3 |