| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:51804103-51804236 | Common:2; Rare:41 | ||||
| chr13:52012106-52012428 | Common:2; Rare:104; Clinvar:1 | ||||
| chr13:52450590-52450694 | Rare:34 | ||||
| chr13:52455329-52455501 | Common:3; Rare:57 | ||||
| chr13:52455953-52456001 | Common:1; Rare:16 | ||||
| chr13:60397110-60397380 | Common:4; Rare:102 | ||||
| chr13:72727591-72727950 | Common:4; Rare:134 | ||||
| chr13:72781843-72782188 | Common:1; Rare:132 | ||||
| chr13:76992012-76992181 | Common:1; Rare:78; Clinvar:12; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr13:77027137-77027289 | Common:5; Rare:47 | ||||
| chr13:77918567-77918932 | Common:2; Rare:82; Clinvar (benign):2 | ||||
| chr13:79405770-79405885 | Rare:44 | ||||
| chr13:79406219-79406314 | Common:1; Rare:29 | ||||
| chr13:79481030-79481378 | Common:2; Rare:138 | ||||
| chr13:94601550-94601907 | Common:4; Rare:105 |