| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:30464195-30464349 | Common:1; Rare:44 | ||||
| chr13:30464868-30464994 | Common:1; Rare:36 | ||||
| chr13:30465760-30466128 | Common:1; Rare:113 | ||||
| chr13:30617255-30617403 | Rare:32 | ||||
| chr13:30617474-30618074 | Common:1; Rare:187 | ||||
| chr13:30932560-30932718 | Rare:37 | ||||
| chr13:31161701-31162105 | Common:1; Rare:178 | ||||
| chr13:31162279-31162520 | Common:2; Rare:73 | ||||
| chr13:32315416-32315583 | Rare:47; Clinvar:2; Clinvar (benign):2 | ||||
| chr13:32428116-32428242 | Rare:24 | ||||
| chr13:32538674-32538869 | Common:1; Rare:62 | ||||
| chr13:32539154-32539193 | Rare:11 | ||||
| chr13:32586220-32586593 | Common:2; Rare:114 | ||||
| chr13:33285686-33285851 | Rare:30 | ||||
| chr13:33818013-33818208 | Common:1; Rare:87 |