| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:52012105-52012428 | Common:2; Rare:104; Clinvar:1 | ||||
| chr13:52159558-52159718 | Common:1; Rare:26 | ||||
| chr13:52406157-52406313 | Common:2; Rare:38 | ||||
| chr13:52450548-52450771 | Common:1; Rare:64 | ||||
| chr13:52455189-52455543 | Common:4; Rare:111 | ||||
| chr13:52455926-52456017 | Common:1; Rare:31 | ||||
| chr13:52652234-52652416 | Common:3; Rare:48 | ||||
| chr13:52652658-52652963 | Common:3; Rare:103 | ||||
| chr13:52653085-52653188 | Common:1; Rare:33 | ||||
| chr13:60163732-60164119 | Common:2; Rare:104; Clinvar (benign):1 | ||||
| chr13:60396922-60397052 | Rare:28 | ||||
| chr13:60397122-60397380 | Common:4; Rare:95 | ||||
| chr13:71866296-71866630 | Common:4; Rare:132; Clinvar:1 | ||||
| chr13:71867251-71867495 | Common:1; Rare:53 | ||||
| chr13:72727543-72728007 | Common:7; Rare:185 |