| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:18571496-18571971 | Common:26; Rare:781 | ||||
| chr19:18572438-18572662 | Common:3; Rare:49 | ||||
| chr19:18588015-18588415 | Common:1; Rare:115 | ||||
| chr19:18588480-18588880 | Common:19; Rare:354 | ||||
| chr19:18588980-18590510 | Common:31; Rare:818 | ||||
| chr19:18594219-18594940 | Common:4; Rare:321; Clinvar (pathogenic):3 | ||||
| chr19:18636666-18637098 | Common:8; Rare:347 | ||||
| chr19:18683371-18684129 | Common:11; Rare:647 | ||||
| chr19:18831680-18832092 | Common:7; Rare:499 | ||||
| chr19:18832146-18832630 | Common:2; Rare:230 | ||||
| chr19:18832680-18832970 | Common:1; Rare:147 | ||||
| chr19:18883763-18884310 | Common:2; Rare:442; Clinvar:8; Clinvar (benign):16; Clinvar (pathogenic):4 | ||||
| chr19:18895132-18895902 | Common:6; Rare:247; Clinvar (benign):3 | ||||
| chr19:18896080-18896310 | Rare:52 | ||||
| chr19:18918143-18918856 | Common:7; Rare:147 |