| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:47144388-47144563 | Rare:42 | ||||
| chr16:47460851-47461432 | Common:3; Rare:228; Clinvar:1; Clinvar (benign):3 | ||||
| chr16:47461703-47461854 | Rare:32 | ||||
| chr16:47461928-47462219 | Common:1; Rare:47 | ||||
| chr16:48244165-48244427 | Common:3; Rare:89 | ||||
| chr16:48244430-48244644 | Rare:52 | ||||
| chr16:48244921-48244960 | Rare:6 | ||||
| chr16:48365824-48366310 | Common:5; Rare:132 | ||||
| chr16:48384941-48385235 | Common:2; Rare:94 | ||||
| chr16:48385242-48385669 | Common:3; Rare:163 | ||||
| chr16:48385708-48385843 | Common:1; Rare:48 | ||||
| chr16:48385860-48386130 | Rare:57 | ||||
| chr16:48609645-48609859 | Rare:67 | ||||
| chr16:48609920-48610013 | Rare:28 | ||||
| chr16:48610025-48610547 | Common:5; Rare:150 |