Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:42833102-42833482 | Rare:110 | ||||
chr17:43006519-43006773 | Rare:49 | ||||
chr17:43125344-43125654 | Rare:74; Clinvar:3; Clinvar (benign):2 | ||||
chr17:43171024-43171245 | Rare:68 | ||||
chr17:44070619-44070911 | Common:3; Rare:98; Clinvar:4; Clinvar (benign):2 | ||||
chr17:44111237-44111449 | Rare:55 | ||||
chr17:44186691-44187002 | Rare:104 | ||||
chr17:44187153-44187274 | Rare:31 | ||||
chr17:44268093-44268365 | Rare:57; Clinvar:3 | ||||
chr17:44324760-44324966 | Common:2; Rare:74 | ||||
chr17:44350506-44350759 | Rare:90; Clinvar:4; Clinvar (benign):3 | ||||
chr17:44503369-44503713 | Rare:134 | ||||
chr17:44899379-44899774 | Common:3; Rare:125; Clinvar:3; Clinvar (benign):1 | ||||
chr17:45060971-45061345 | Common:2; Rare:102 | ||||
chr17:45132552-45132631 | Rare:31 |