| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:34942050-34942360 | Common:3; Rare:91 | ||||
| chr13:36214300-36214810 | Common:7; Rare:373 | ||||
| chr13:36297433-36297720 | Common:6; Rare:111 | ||||
| chr13:36297740-36298220 | Common:9; Rare:460 | ||||
| chr13:36345405-36346372 | Common:18; Rare:659; Clinvar:1; Clinvar (benign):6 | ||||
| chr13:36346280-36346590 | Common:13; Rare:298; Clinvar:10; Clinvar (benign):8 | ||||
| chr13:36346642-36347042 | Common:16; Rare:312 | ||||
| chr13:36818960-36819360 | Common:5; Rare:505; Clinvar:15 | ||||
| chr13:36920130-36920490 | Common:10; Rare:148; Clinvar:6; Clinvar (benign):2 | ||||
| chr13:36999205-36999605 | Common:1; Rare:586 | ||||
| chr13:36999940-37000400 | Common:7; Rare:243 | ||||
| chr13:37000480-37001292 | Common:14; Rare:752; Clinvar (pathogenic):6 | ||||
| chr13:37059507-37059907 | Common:7; Rare:329 | ||||
| chr13:38349401-38350513 | Common:32; Rare:1307; Clinvar (pathogenic):4 | ||||
| chr13:39036458-39036858 | Common:1; Rare:87 |