| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:46689111-46689330 | Common:2; Rare:164; Clinvar:4; Clinvar (benign):2 | ||||
| chr16:46689504-46689728 | Common:4; Rare:174; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr16:46789800-46790250 | Common:9; Rare:147 | ||||
| chr16:46831121-46831283 | Common:4; Rare:123 | ||||
| chr16:46884042-46884437 | Common:4; Rare:206 | ||||
| chr16:46973606-46973820 | Rare:189 | ||||
| chr16:47143905-47144097 | Rare:170 | ||||
| chr16:47460838-47461393 | Common:5; Rare:354; Clinvar (benign):5 | ||||
| chr16:48244083-48244563 | Common:5; Rare:220 | ||||
| chr16:48365883-48366117 | Common:10; Rare:131 | ||||
| chr16:48385273-48385608 | Common:6; Rare:237 | ||||
| chr16:48610142-48610358 | Common:5; Rare:146 | ||||
| chr16:50024942-50025309 | Common:5; Rare:115 | ||||
| chr16:50065827-50066014 | Common:4; Rare:64 | ||||
| chr16:50152858-50152963 | Rare:41 |