| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:35196217-35196502 | Common:1; Rare:42 | ||||
| chr20:35395853-35396144 | Rare:46 | ||||
| chr20:35448188-35448392 | Rare:35 | ||||
| chr20:35466981-35467182 | Common:2; Rare:69; Clinvar (pathogenic):1 | ||||
| chr20:35479212-35479683 | Rare:116 | ||||
| chr20:35479697-35480078 | Common:1; Rare:85 | ||||
| chr20:35490922-35491053 | Rare:27 | ||||
| chr20:35546418-35546439 | Common:1; Rare:4 | ||||
| chr20:35548512-35548870 | Rare:111 | ||||
| chr20:35624190-35624378 | Common:1; Rare:36 | ||||
| chr20:35663792-35664022 | Rare:55 | ||||
| chr20:35700957-35701141 | Common:1; Rare:32 | ||||
| chr20:35704451-35704821 | Rare:87 | ||||
| chr20:35709196-35709469 | Rare:38 | ||||
| chr20:35712033-35712174 | Rare:27 |