| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:21233588-21233731 | Rare:31 | ||||
| chr16:21652594-21652712 | Rare:32 | ||||
| chr16:21952991-21953419 | Common:1; Rare:109; Clinvar (benign):3 | ||||
| chr16:22436939-22437325 | Rare:136 | ||||
| chr16:22437461-22437695 | Common:2; Rare:61 | ||||
| chr16:23452725-23452819 | Rare:37; Clinvar (benign):1 | ||||
| chr16:23557304-23557483 | Common:2; Rare:82; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:23641237-23641545 | Common:2; Rare:90; Clinvar:1; Clinvar (benign):3 | ||||
| chr16:23678714-23678944 | Common:4; Rare:72 | ||||
| chr16:24729611-24729745 | Common:6; Rare:72 | ||||
| chr16:25111468-25111797 | Common:2; Rare:84 | ||||
| chr16:27268713-27268872 | Common:1; Rare:57 | ||||
| chr16:27313804-27313985 | Common:2; Rare:51 | ||||
| chr16:27549891-27550167 | Common:2; Rare:101 | ||||
| chr16:28491305-28491456 | Common:1; Rare:37 |