Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:44797745-44798007 | Rare:54 | ||||
chr17:47100271-47100414 | Common:1; Rare:35 | ||||
chr17:47492443-47492753 | Common:3; Rare:106 | ||||
chr17:48546455-48546552 | Rare:13 | ||||
chr17:49691200-49691336 | Common:2; Rare:27 | ||||
chr17:50189874-50190074 | Common:1; Rare:57; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr17:50866919-50867128 | Common:1; Rare:43 | ||||
chr17:50944615-50944765 | Rare:35 | ||||
chr17:57834517-57834613 | Rare:11 | ||||
chr17:57851783-57851984 | Common:1; Rare:32 | ||||
chr17:58324375-58324533 | Rare:43 | ||||
chr17:58324917-58325076 | Rare:36 | ||||
chr17:58631834-58632132 | Common:3; Rare:125 | ||||
chr17:58659301-58659567 | Common:2; Rare:87 | ||||
chr17:60134876-60135039 | Rare:25 |