| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:22437119-22437326 | Rare:69 | ||||
| chr16:22437447-22437483 | Rare:11 | ||||
| chr16:22437505-22437671 | Common:2; Rare:42 | ||||
| chr16:22814774-22815010 | Common:1; Rare:79 | ||||
| chr16:23452725-23452794 | Rare:22 | ||||
| chr16:23557325-23557592 | Common:3; Rare:95; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:23641223-23641546 | Common:2; Rare:92; Clinvar:1; Clinvar (benign):3 | ||||
| chr16:24729604-24729745 | Common:6; Rare:74 | ||||
| chr16:25111468-25111805 | Common:2; Rare:91 | ||||
| chr16:27268719-27268851 | Common:1; Rare:42 | ||||
| chr16:27549850-27550167 | Common:2; Rare:123 | ||||
| chr16:28491915-28492138 | Common:2; Rare:52; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:28494297-28494684 | Common:1; Rare:80 | ||||
| chr16:28824006-28824169 | Common:2; Rare:48 | ||||
| chr16:28846216-28846696 | Common:2; Rare:161; Clinvar:7; Clinvar (benign):6 |