Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:36370355-36370561 | Common:2; Rare:35 | ||||
chr13:37000231-37000397 | Common:2; Rare:30 | ||||
chr13:37000732-37000816 | Rare:34; Clinvar (pathogenic):1 | ||||
chr13:37059584-37059754 | Common:1; Rare:55 | ||||
chr13:38350254-38350363 | Rare:32 | ||||
chr13:39038086-39038406 | Common:1; Rare:81 | ||||
chr13:40789370-40789609 | Common:2; Rare:79; Clinvar:5; Clinvar (benign):2 | ||||
chr13:41060868-41061635 | Common:20; Rare:308 | ||||
chr13:41061671-41061839 | Common:1; Rare:66 | ||||
chr13:41132732-41132980 | Rare:68 | ||||
chr13:42271794-42272022 | Common:2; Rare:69 | ||||
chr13:43786764-43786783 | Rare:2 | ||||
chr13:43879440-43879654 | Common:1; Rare:52 | ||||
chr13:43879665-43879975 | Common:18; Rare:80 | ||||
chr13:44436806-44436997 | Common:2; Rare:59 |