| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:48233002-48233363 | Common:3; Rare:119 | ||||
| chr13:48233376-48233700 | Common:3; Rare:88 | ||||
| chr13:48303049-48303279 | Common:1; Rare:36 | ||||
| chr13:48303304-48304093 | Common:1; Rare:222; Clinvar:16; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr13:48304198-48304526 | Rare:65 | ||||
| chr13:48532050-48532356 | Common:2; Rare:63 | ||||
| chr13:48532457-48532532 | Rare:26 | ||||
| chr13:48532613-48532937 | Common:4; Rare:115 | ||||
| chr13:48532949-48533192 | Common:2; Rare:76 | ||||
| chr13:48975462-48975506 | Rare:11 | ||||
| chr13:49110205-49110420 | Common:2; Rare:67 | ||||
| chr13:49110645-49110737 | Rare:20 | ||||
| chr13:49247547-49247577 | Rare:9 | ||||
| chr13:49247698-49248076 | Common:1; Rare:91 | ||||
| chr13:49443568-49443746 | Rare:26 |