Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:39927539-39927745 | Common:2; Rare:60 | ||||
chr17:40140150-40140565 | Common:5; Rare:195 | ||||
chr17:41812782-41813039 | Rare:63; Clinvar:3 | ||||
chr17:41966586-41966837 | Common:1; Rare:86 | ||||
chr17:42017382-42017482 | Rare:45 | ||||
chr17:42458751-42458920 | Common:1; Rare:64 | ||||
chr17:42566957-42567130 | Common:3; Rare:58 | ||||
chr17:42577671-42577839 | Rare:83 | ||||
chr17:42609333-42609705 | Common:8; Rare:150; Clinvar (benign):1 | ||||
chr17:42761092-42761236 | Rare:38 | ||||
chr17:42833340-42833479 | Rare:51 | ||||
chr17:43171043-43171245 | Rare:61 | ||||
chr17:44070608-44070925 | Common:3; Rare:109; Clinvar:4; Clinvar (benign):2 | ||||
chr17:44186673-44186998 | Common:1; Rare:115 | ||||
chr17:44187178-44187274 | Rare:26 |