Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:842445-842988 | Common:8; Rare:222 | ||||
chr11:844014-844159 | Common:1; Rare:34 | ||||
chr11:844228-844442 | Common:3; Rare:61 | ||||
chr11:1838747-1839030 | Common:1; Rare:78; Clinvar:1 | ||||
chr11:1919551-1919754 | Rare:54; Clinvar:2; Clinvar (benign):1 | ||||
chr11:2137276-2137422 | Rare:35 | ||||
chr11:2138328-2138585 | Common:2; Rare:63 | ||||
chr11:2138607-2138668 | Rare:15 | ||||
chr11:2138864-2139068 | Common:1; Rare:35 | ||||
chr11:2992228-2992522 | Common:2; Rare:113 | ||||
chr11:3057369-3057538 | Rare:59 | ||||
chr11:3379088-3379309 | Common:3; Rare:58 | ||||
chr11:3840910-3841073 | Rare:72 | ||||
chr11:4094594-4094877 | Common:2; Rare:78 | ||||
chr11:4393658-4393814 | Rare:37 |