| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:88804218-88804819 | Common:5; Rare:348; Clinvar (benign):5 | ||||
| chr16:88811590-88811850 | Common:8; Rare:154; Clinvar (benign):4 | ||||
| chr16:88811862-88812100 | Common:4; Rare:164; Clinvar (benign):2 | ||||
| chr16:88856867-88857178 | Common:8; Rare:281; Clinvar:4; Clinvar (benign):4 | ||||
| chr16:89093769-89093976 | Common:6; Rare:164 | ||||
| chr16:89200040-89200620 | Common:1; Rare:152 | ||||
| chr16:89217572-89217765 | Common:2; Rare:172 | ||||
| chr16:89490508-89490981 | Common:12; Rare:335 | ||||
| chr16:89508243-89508541 | Common:4; Rare:246; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr16:89560497-89560786 | Rare:243 | ||||
| chr16:89575096-89575283 | Common:2; Rare:51 | ||||
| chr16:89575657-89576083 | Common:4; Rare:184 | ||||
| chr16:89657632-89658152 | Common:7; Rare:490 | ||||
| chr16:89686477-89686711 | Common:18; Rare:183 | ||||
| chr16:89686898-89687153 | Common:3; Rare:139 |