| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:51804113-51804244 | Common:2; Rare:41 | ||||
| chr13:52012106-52012421 | Common:2; Rare:101; Clinvar:1 | ||||
| chr13:52159551-52159719 | Common:1; Rare:28 | ||||
| chr13:52455344-52455616 | Common:3; Rare:104 | ||||
| chr13:52455926-52456021 | Common:1; Rare:33 | ||||
| chr13:52652386-52652926 | Common:3; Rare:159 | ||||
| chr13:52739593-52739680 | Rare:37 | ||||
| chr13:52739853-52740160 | Common:1; Rare:60 | ||||
| chr13:60163855-60164118 | Common:2; Rare:70 | ||||
| chr13:60397173-60397380 | Common:4; Rare:76 | ||||
| chr13:72727598-72727978 | Common:4; Rare:146 | ||||
| chr13:72781869-72782273 | Common:1; Rare:141 | ||||
| chr13:75549378-75549827 | Common:9; Rare:119 | ||||
| chr13:76992051-76992175 | Rare:57; Clinvar:7; Clinvar (benign):6 | ||||
| chr13:77918782-77918908 | Common:1; Rare:30 |