| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:52159211-52159285 | Common:2; Rare:15 | ||||
| chr13:52159404-52159540 | Common:2; Rare:53 | ||||
| chr13:52449973-52450250 | Common:1; Rare:69 | ||||
| chr13:52450515-52450727 | Common:1; Rare:66 | ||||
| chr13:52455250-52455582 | Common:3; Rare:122 | ||||
| chr13:52455892-52456008 | Common:2; Rare:41 | ||||
| chr13:52652072-52652451 | Common:3; Rare:101 | ||||
| chr13:52652523-52653008 | Common:3; Rare:149 | ||||
| chr13:52653096-52653201 | Common:1; Rare:35 | ||||
| chr13:60163565-60163625 | Common:1; Rare:19; Clinvar (benign):1 | ||||
| chr13:60163684-60164231 | Common:2; Rare:152; Clinvar (benign):1 | ||||
| chr13:60395993-60396106 | Rare:24 | ||||
| chr13:60396221-60396565 | Common:2; Rare:131 | ||||
| chr13:60396867-60397261 | Rare:117 | ||||
| chr13:60397397-60397709 | Common:3; Rare:110 |