| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:49956683-49956989 | Common:2; Rare:39 | ||||
| chr13:50005517-50005543 | Rare:4 | ||||
| chr13:52194378-52194487 | Rare:33 | ||||
| chr13:72971490-72971788 | Common:2; Rare:62 | ||||
| chr13:73059316-73059586 | Rare:63 | ||||
| chr13:73062649-73062993 | Common:8; Rare:114 | ||||
| chr13:73064174-73064466 | Common:2; Rare:51 | ||||
| chr13:73194380-73194595 | Common:3; Rare:35 | ||||
| chr13:79441754-79441957 | Common:3; Rare:35 | ||||
| chr13:79485284-79485302 | Rare:3 | ||||
| chr13:79988687-79988822 | Rare:28 | ||||
| chr13:93227446-93227520 | Common:1; Rare:21; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:98572201-98572547 | Common:2; Rare:58 | ||||
| chr13:98650404-98650707 | Common:2; Rare:62 | ||||
| chr13:99087946-99088051 | Common:1; Rare:25 |