| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:33494910-33495240 | Common:2; Rare:56 | ||||
| chr13:33542393-33542745 | Rare:116 | ||||
| chr13:33542867-33543044 | Common:2; Rare:47 | ||||
| chr13:33697570-33697860 | Rare:49 | ||||
| chr13:33723800-33724110 | Common:3; Rare:58 | ||||
| chr13:33761490-33762170 | Common:6; Rare:128 | ||||
| chr13:33937880-33938170 | Rare:54 | ||||
| chr13:34004941-34005091 | Rare:69 | ||||
| chr13:34155938-34156087 | Common:4; Rare:23 | ||||
| chr13:34156894-34157310 | Common:2; Rare:84 | ||||
| chr13:34847810-34848080 | Common:3; Rare:57 | ||||
| chr13:36762310-36762570 | Common:3; Rare:31 | ||||
| chr13:36872610-36872910 | Rare:109; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr13:40664738-40664897 | Common:3; Rare:41 | ||||
| chr13:40665518-40665650 | Rare:31 |