Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:30617229-30617403 | Rare:36 | ||||
chr13:30617473-30618005 | Common:1; Rare:173 | ||||
chr13:31162337-31162461 | Common:1; Rare:34 | ||||
chr13:32315426-32315584 | Rare:45; Clinvar:2; Clinvar (benign):2 | ||||
chr13:32315802-32315989 | Common:3; Rare:41; Clinvar (benign):3 | ||||
chr13:32538674-32538973 | Common:1; Rare:81 | ||||
chr13:32586220-32586590 | Common:2; Rare:112 | ||||
chr13:33285651-33285913 | Rare:63 | ||||
chr13:33817997-33818244 | Common:1; Rare:112 | ||||
chr13:34942186-34942298 | Common:2; Rare:35 | ||||
chr13:35476311-35476405 | Rare:19 | ||||
chr13:35476659-35476960 | Common:1; Rare:42 | ||||
chr13:36131368-36131489 | Rare:34 | ||||
chr13:36297771-36297908 | Rare:51 | ||||
chr13:36345510-36345815 | Common:2; Rare:71 |