| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:46052718-46052842 | Common:2; Rare:33 | ||||
| chr13:46797121-46797303 | Common:3; Rare:70 | ||||
| chr13:48001265-48001408 | Common:1; Rare:66; Clinvar:3; Clinvar (benign):2 | ||||
| chr13:48037610-48037789 | Common:1; Rare:81 | ||||
| chr13:49247844-49247977 | Rare:43 | ||||
| chr13:49585543-49585624 | Common:1; Rare:24 | ||||
| chr13:50081980-50082256 | Common:1; Rare:77 | ||||
| chr13:52455329-52455493 | Common:3; Rare:54 | ||||
| chr13:52652537-52652914 | Common:3; Rare:106 | ||||
| chr13:72727598-72727934 | Common:4; Rare:119 | ||||
| chr13:72781896-72782171 | Common:1; Rare:104 | ||||
| chr13:75549440-75549821 | Common:8; Rare:97 | ||||
| chr13:75636033-75636347 | Common:2; Rare:70 | ||||
| chr13:75760520-75760715 | Common:2; Rare:44 | ||||
| chr13:95676916-95677176 | Common:3; Rare:90 |