Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:18394140-18394400 | Common:1; Rare:49 | ||||
chr11:18394410-18394626 | Common:1; Rare:86; Clinvar (benign):1 | ||||
chr11:18396141-18396418 | Common:1; Rare:109 | ||||
chr11:18412245-18412338 | Common:1; Rare:29 | ||||
chr11:18526825-18526992 | Rare:79 | ||||
chr11:18588650-18588915 | Common:2; Rare:94 | ||||
chr11:18588972-18589231 | Rare:56 | ||||
chr11:18634278-18634585 | Common:3; Rare:107 | ||||
chr11:18634789-18634874 | Rare:15 | ||||
chr11:18698558-18698803 | Common:6; Rare:64 | ||||
chr11:18706393-18706511 | Rare:18 | ||||
chr11:19116939-19117276 | Common:3; Rare:92 | ||||
chr11:19777063-19777486 | Common:3; Rare:110 | ||||
chr11:19777528-19777849 | Common:2; Rare:81 | ||||
chr11:20387389-20387806 | Common:8; Rare:139 |