| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:34942000-34942343 | Common:3; Rare:97 | ||||
| chr13:36131272-36131404 | Common:1; Rare:25 | ||||
| chr13:36297384-36297558 | Common:3; Rare:25 | ||||
| chr13:36297624-36297727 | Common:1; Rare:35 | ||||
| chr13:36297740-36298028 | Common:3; Rare:100 | ||||
| chr13:36298132-36298222 | Rare:15 | ||||
| chr13:36345198-36345266 | Rare:20 | ||||
| chr13:36345487-36345807 | Common:2; Rare:79 | ||||
| chr13:36345838-36345975 | Common:1; Rare:29 | ||||
| chr13:36345988-36346071 | Rare:21 | ||||
| chr13:36346073-36346595 | Common:4; Rare:131; Clinvar:3; Clinvar (benign):3 | ||||
| chr13:36346609-36346952 | Common:4; Rare:96 | ||||
| chr13:36431687-36431914 | Rare:64 | ||||
| chr13:36673834-36674097 | Common:1; Rare:83 | ||||
| chr13:36819068-36819323 | Common:1; Rare:96; Clinvar:3 |