| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:75635766-75635883 | Common:1; Rare:29 | ||||
| chr13:75635921-75636720 | Common:3; Rare:206 | ||||
| chr13:77027131-77027284 | Common:5; Rare:50 | ||||
| chr13:77918779-77918932 | Common:1; Rare:37 | ||||
| chr13:79405782-79405901 | Rare:41 | ||||
| chr13:79406190-79406334 | Common:4; Rare:46 | ||||
| chr13:93226776-93227431 | Common:3; Rare:142; Clinvar:6; Clinvar (benign):2 | ||||
| chr13:95301254-95301539 | Common:2; Rare:89 | ||||
| chr13:95301744-95301870 | Common:1; Rare:28 | ||||
| chr13:95676955-95677292 | Common:4; Rare:115 | ||||
| chr13:96053353-96053561 | Common:2; Rare:88 | ||||
| chr13:99200670-99200909 | Common:6; Rare:115 | ||||
| chr13:100088909-100089207 | Rare:116; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr13:102596798-102597045 | Common:1; Rare:117; Clinvar (benign):1 | ||||
| chr13:102798943-102799211 | Common:1; Rare:56 |