| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:29833743-29834013 | Common:1; Rare:79 | ||||
| chr16:29863211-29863589 | Common:1; Rare:96 | ||||
| chr16:29863647-29863978 | Common:1; Rare:75 | ||||
| chr16:29899176-29899329 | Common:1; Rare:28 | ||||
| chr16:29900215-29900522 | Common:2; Rare:77 | ||||
| chr16:29926015-29926353 | Common:3; Rare:125 | ||||
| chr16:29961958-29962257 | Common:1; Rare:94 | ||||
| chr16:29962775-29963277 | Common:3; Rare:132 | ||||
| chr16:29973529-29973918 | Common:5; Rare:127 | ||||
| chr16:29974123-29974340 | Rare:53 | ||||
| chr16:29995596-29995765 | Rare:72 | ||||
| chr16:29996064-29996313 | Common:2; Rare:91 | ||||
| chr16:30023192-30023404 | Common:2; Rare:49 | ||||
| chr16:30052902-30053178 | Common:1; Rare:82 | ||||
| chr16:30064036-30064497 | Common:1; Rare:90; Clinvar (benign):1 |