Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:43491225-43491471 | Rare:48 | ||||
chr17:44070618-44070911 | Common:3; Rare:98; Clinvar:4; Clinvar (benign):2 | ||||
chr17:44123613-44123854 | Common:3; Rare:68 | ||||
chr17:44186689-44187050 | Common:1; Rare:117 | ||||
chr17:44187142-44187328 | Common:1; Rare:48 | ||||
chr17:44212924-44213225 | Common:1; Rare:60 | ||||
chr17:44220845-44221084 | Rare:79 | ||||
chr17:44221273-44221402 | Rare:39 | ||||
chr17:44222094-44222346 | Rare:53 | ||||
chr17:44324774-44325017 | Common:2; Rare:87 | ||||
chr17:44503383-44503713 | Rare:132 | ||||
chr17:44899371-44899473 | Rare:42 | ||||
chr17:45060964-45061353 | Common:2; Rare:109 | ||||
chr17:45148160-45148478 | Common:1; Rare:93 | ||||
chr17:45161500-45161813 | Common:1; Rare:81 |