| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:41061395-41061586 | Common:2; Rare:51 | ||||
| chr13:43879493-43879647 | Rare:41 | ||||
| chr13:43879743-43879847 | Common:14; Rare:41 | ||||
| chr13:44989443-44989607 | Rare:62 | ||||
| chr13:45120180-45120560 | Common:2; Rare:91 | ||||
| chr13:45341040-45341599 | Common:4; Rare:257 | ||||
| chr13:46052722-46052815 | Common:1; Rare:25 | ||||
| chr13:48001246-48001405 | Common:1; Rare:74; Clinvar:3; Clinvar (benign):4 | ||||
| chr13:48037644-48037789 | Common:1; Rare:70 | ||||
| chr13:48975637-48975923 | Common:2; Rare:89 | ||||
| chr13:48976554-48976662 | Rare:36 | ||||
| chr13:49247807-49247976 | Rare:48 | ||||
| chr13:49495875-49496055 | Rare:43 | ||||
| chr13:50081935-50082296 | Common:1; Rare:100 | ||||
| chr13:51804103-51804176 | Common:2; Rare:24 |