| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:88857569-88857711 | Common:1; Rare:36 | ||||
| chr16:89093698-89093995 | Common:6; Rare:119 | ||||
| chr16:89201632-89202025 | Common:4; Rare:142 | ||||
| chr16:89217514-89217773 | Common:1; Rare:128 | ||||
| chr16:89489183-89489527 | Common:6; Rare:131 | ||||
| chr16:89489559-89489653 | Rare:35 | ||||
| chr16:89490441-89491024 | Common:6; Rare:204 | ||||
| chr16:89491082-89491209 | Common:1; Rare:37 | ||||
| chr16:89491668-89491772 | Rare:22 | ||||
| chr16:89507439-89507669 | Rare:72 | ||||
| chr16:89507674-89507766 | Common:2; Rare:42 | ||||
| chr16:89507769-89507965 | Common:1; Rare:78 | ||||
| chr16:89507968-89508125 | Rare:51 | ||||
| chr16:89508150-89508489 | Common:4; Rare:162; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:89508835-89509017 | Rare:85 |