| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:2046944-2047231 | Common:2; Rare:68 | ||||
| chr16:2047239-2047730 | Rare:276; Clinvar (benign):1 | ||||
| chr16:2047726-2048126 | Rare:991; Clinvar:14; Clinvar (benign):31; Clinvar (pathogenic):2 | ||||
| chr16:2135811-2136211 | Common:4; Rare:574; Clinvar (benign):1 | ||||
| chr16:2140584-2140984 | Common:5; Rare:129 | ||||
| chr16:2148359-2148775 | Rare:334 | ||||
| chr16:2150778-2151372 | Common:11; Rare:314 | ||||
| chr16:2152368-2152915 | Common:5; Rare:350 | ||||
| chr16:2153202-2153602 | Common:4; Rare:376 | ||||
| chr16:2154951-2155853 | Common:13; Rare:1408 | ||||
| chr16:2155809-2156643 | Common:10; Rare:430 | ||||
| chr16:2196420-2197061 | Common:4; Rare:638 | ||||
| chr16:2204910-2205230 | Common:4; Rare:191 | ||||
| chr16:2205249-2205661 | Common:6; Rare:298 | ||||
| chr16:2205612-2205889 | Common:27; Rare:649 |