| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30748128-30748462 | Common:2; Rare:81; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:30762054-30762334 | Common:3; Rare:93 | ||||
| chr16:30768836-30769321 | Rare:131 | ||||
| chr16:30893855-30894265 | Common:5; Rare:110 | ||||
| chr16:30922642-30922857 | Common:1; Rare:65 | ||||
| chr16:30923228-30923610 | Common:1; Rare:89 | ||||
| chr16:30957514-30957983 | Common:1; Rare:139 | ||||
| chr16:30984956-30985268 | Common:1; Rare:85 | ||||
| chr16:31033453-31033831 | Common:1; Rare:108 | ||||
| chr16:31033930-31034112 | Rare:54 | ||||
| chr16:31073716-31073837 | Rare:38 | ||||
| chr16:31074192-31074464 | Common:1; Rare:75 | ||||
| chr16:31189664-31190399 | Common:2; Rare:205; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:31190747-31191110 | Common:1; Rare:119; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr16:31202284-31202359 | Common:2; Rare:20 |