| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:49443996-49444442 | Common:1; Rare:142 | ||||
| chr13:49792530-49792706 | Common:4; Rare:70 | ||||
| chr13:50081992-50082296 | Common:1; Rare:86 | ||||
| chr13:51453018-51453359 | Rare:124 | ||||
| chr13:51804112-51804282 | Common:2; Rare:50 | ||||
| chr13:52012106-52012418 | Common:2; Rare:101; Clinvar:1 | ||||
| chr13:52455375-52455507 | Common:2; Rare:43 | ||||
| chr13:52652666-52652916 | Common:3; Rare:80 | ||||
| chr13:60163877-60164071 | Common:1; Rare:47 | ||||
| chr13:72727585-72727972 | Common:5; Rare:150 | ||||
| chr13:72781859-72782188 | Common:1; Rare:128 | ||||
| chr13:75635730-75635831 | Common:1; Rare:23 | ||||
| chr13:75636048-75636386 | Common:2; Rare:78 | ||||
| chr13:76991997-76992107 | Common:2; Rare:56; Clinvar:11; Clinvar (benign):7 | ||||
| chr13:77027142-77027282 | Common:5; Rare:43 |