| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:17859644-17859969 | Common:2; Rare:102 | ||||
| chr19:17932740-17933048 | Common:2; Rare:75 | ||||
| chr19:18153012-18153283 | Common:1; Rare:91 | ||||
| chr19:18323019-18323308 | Common:3; Rare:94 | ||||
| chr19:18340500-18340640 | Common:3; Rare:55 | ||||
| chr19:18557685-18557911 | Common:4; Rare:59 | ||||
| chr19:18571679-18571891 | Common:2; Rare:92 | ||||
| chr19:18683486-18683694 | Common:1; Rare:68 | ||||
| chr19:18919352-18919771 | Common:3; Rare:151 | ||||
| chr19:19033482-19033649 | Common:2; Rare:51 | ||||
| chr19:19192122-19192264 | Common:1; Rare:44 | ||||
| chr19:19192632-19192976 | Common:2; Rare:81 | ||||
| chr19:19516167-19516278 | Rare:64; Clinvar (pathogenic):1 | ||||
| chr19:19733084-19733217 | Common:1; Rare:30 | ||||
| chr19:19821668-19821900 | Common:1; Rare:80 |