| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:29663154-29663265 | Rare:18 | ||||
| chr16:29790513-29790801 | Common:1; Rare:117; Clinvar (benign):2 | ||||
| chr16:29816003-29816230 | Common:1; Rare:63 | ||||
| chr16:29816279-29816604 | Common:1; Rare:107 | ||||
| chr16:29961676-29961704 | Rare:4 | ||||
| chr16:29961947-29962161 | Common:1; Rare:70 | ||||
| chr16:29973579-29973899 | Common:4; Rare:100 | ||||
| chr16:29995596-29995713 | Rare:53 | ||||
| chr16:29996064-29996296 | Common:2; Rare:82 | ||||
| chr16:30053026-30053211 | Common:1; Rare:70; Clinvar (benign):1 | ||||
| chr16:30064093-30064446 | Common:1; Rare:69; Clinvar (benign):1 | ||||
| chr16:30065566-30065835 | Rare:93 | ||||
| chr16:30075887-30076051 | Rare:55 | ||||
| chr16:30091908-30092119 | Common:1; Rare:49 | ||||
| chr16:30183492-30183644 | Common:2; Rare:38 |