| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:33285625-33285890 | Common:1; Rare:97 | ||||
| chr13:33818007-33818236 | Common:2; Rare:203 | ||||
| chr13:36297730-36298050 | Common:5; Rare:197 | ||||
| chr13:36345520-36346070 | Common:4; Rare:193 | ||||
| chr13:36346086-36346360 | Common:3; Rare:97; Clinvar:1; Clinvar (benign):2 | ||||
| chr13:36346280-36346630 | Common:4; Rare:133; Clinvar:5; Clinvar (benign):3 | ||||
| chr13:36920028-36920332 | Common:9; Rare:198; Clinvar:11; Clinvar (benign):4 | ||||
| chr13:36999258-36999468 | Rare:164 | ||||
| chr13:37000243-37000422 | Common:4; Rare:64 | ||||
| chr13:37000518-37000817 | Common:3; Rare:96; Clinvar (pathogenic):1 | ||||
| chr13:37059569-37059754 | Common:2; Rare:121 | ||||
| chr13:38349402-38350017 | Common:11; Rare:341; Clinvar (pathogenic):2 | ||||
| chr13:38350100-38350590 | Common:3; Rare:196 | ||||
| chr13:39037985-39038495 | Common:2; Rare:255 | ||||
| chr13:39655464-39655802 | Common:6; Rare:221; Clinvar:6; Clinvar (benign):10; Clinvar (pathogenic):2 |