| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:89701693-89701813 | Rare:47 | ||||
| chr16:89720865-89721000 | Common:1; Rare:36 | ||||
| chr16:89816625-89816801 | Common:3; Rare:86; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:89873492-89873697 | Common:1; Rare:93 | ||||
| chr16:89923171-89923362 | Rare:75 | ||||
| chr16:89972482-89972669 | Common:1; Rare:70 | ||||
| chr16:90022594-90022709 | Rare:47 | ||||
| chr17:714785-714982 | Common:3; Rare:64 | ||||
| chr17:752251-752347 | Common:1; Rare:29 | ||||
| chr17:996781-997164 | Common:2; Rare:116 | ||||
| chr17:1400048-1400311 | Common:2; Rare:102 | ||||
| chr17:1516628-1516960 | Common:1; Rare:118 | ||||
| chr17:1684792-1685048 | Common:2; Rare:80; Clinvar:4; Clinvar (benign):1 | ||||
| chr17:1829842-1830071 | Common:7; Rare:92 | ||||
| chr17:2303504-2303549 | Rare:18 |