| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:28718813-28719159 | Common:1; Rare:89 | ||||
| chr13:30306840-30307145 | Common:5; Rare:83 | ||||
| chr13:30307377-30307621 | Common:3; Rare:80 | ||||
| chr13:30465762-30466128 | Common:1; Rare:113 | ||||
| chr13:30616961-30617112 | Rare:27 | ||||
| chr13:30617263-30617392 | Rare:28 | ||||
| chr13:30617460-30618034 | Common:1; Rare:185 | ||||
| chr13:31161836-31161927 | Rare:48 | ||||
| chr13:31162327-31162461 | Common:1; Rare:39 | ||||
| chr13:32031019-32031174 | Rare:33 | ||||
| chr13:32031251-32031453 | Common:1; Rare:56 | ||||
| chr13:32031571-32031790 | Common:1; Rare:64 | ||||
| chr13:32315415-32315583 | Rare:47; Clinvar:2; Clinvar (benign):2 | ||||
| chr13:32315855-32316023 | Common:2; Rare:36; Clinvar (benign):2 | ||||
| chr13:32538682-32538913 | Common:1; Rare:70 |