| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:7629538-7629851 | Common:5; Rare:112; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:8308295-8308638 | Common:2; Rare:108 | ||||
| chr19:8321308-8321653 | Common:2; Rare:151 | ||||
| chr19:8390044-8390413 | Common:1; Rare:105 | ||||
| chr19:8514132-8514227 | Common:1; Rare:29 | ||||
| chr19:9538574-9538743 | Common:1; Rare:52 | ||||
| chr19:9621181-9621569 | Common:3; Rare:113 | ||||
| chr19:9818806-9818846 | Rare:12 | ||||
| chr19:9827832-9827957 | Common:1; Rare:47 | ||||
| chr19:9835013-9835383 | Rare:152 | ||||
| chr19:10380546-10380892 | Common:11; Rare:101; Clinvar:2 | ||||
| chr19:10928409-10928870 | Common:3; Rare:140 | ||||
| chr19:11197505-11197625 | Common:1; Rare:32 | ||||
| chr19:12551472-12551708 | Common:2; Rare:60 | ||||
| chr19:12610723-12610989 | Rare:91 |