| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:29815993-29816225 | Common:1; Rare:67 | ||||
| chr16:29816356-29816528 | Common:1; Rare:58 | ||||
| chr16:29863506-29863656 | Common:2; Rare:38 | ||||
| chr16:29899015-29899318 | Common:2; Rare:63 | ||||
| chr16:29899329-29899640 | Common:1; Rare:58 | ||||
| chr16:29900084-29900741 | Common:5; Rare:154 | ||||
| chr16:29925984-29926339 | Common:3; Rare:136 | ||||
| chr16:29961931-29962165 | Common:1; Rare:79 | ||||
| chr16:29973541-29973931 | Common:5; Rare:126 | ||||
| chr16:29995602-29995713 | Rare:50 | ||||
| chr16:29996072-29996296 | Common:2; Rare:79 | ||||
| chr16:30010940-30011137 | Rare:51 | ||||
| chr16:30021293-30021447 | Rare:29 | ||||
| chr16:30053038-30053163 | Common:1; Rare:44 | ||||
| chr16:30064093-30064490 | Common:1; Rare:80; Clinvar (benign):1 |