| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:88976945-88977258 | Common:1; Rare:85 | ||||
| chr16:89093761-89093945 | Common:3; Rare:82 | ||||
| chr16:89217599-89217740 | Common:1; Rare:70 | ||||
| chr16:89508292-89508426 | Rare:75; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr16:89560555-89560743 | Rare:85 | ||||
| chr16:89657637-89658151 | Common:4; Rare:253 | ||||
| chr16:89686666-89686722 | Common:4; Rare:37 | ||||
| chr16:89720862-89721003 | Common:1; Rare:41 | ||||
| chr16:89816628-89816760 | Common:2; Rare:59; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:89873490-89873725 | Common:1; Rare:106 | ||||
| chr16:89972470-89972669 | Common:1; Rare:72 | ||||
| chr17:714772-714976 | Common:3; Rare:65 | ||||
| chr17:1109069-1109280 | Common:1; Rare:69 | ||||
| chr17:1400055-1400255 | Common:2; Rare:79 | ||||
| chr17:1516596-1516954 | Common:1; Rare:123 |