Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:18394401-18394660 | Common:1; Rare:105; Clinvar (benign):1 | ||||
chr11:18526889-18526963 | Rare:34 | ||||
chr11:18588667-18588860 | Common:2; Rare:66 | ||||
chr11:18634283-18634575 | Common:3; Rare:101 | ||||
chr11:20387417-20387764 | Common:7; Rare:113 | ||||
chr11:26994084-26994196 | Common:1; Rare:21 | ||||
chr11:27506748-27506857 | Common:1; Rare:45 | ||||
chr11:28108130-28108396 | Common:1; Rare:77 | ||||
chr11:30322983-30323173 | Common:1; Rare:57 | ||||
chr11:31369737-31369882 | Rare:45 | ||||
chr11:31509575-31509784 | Common:1; Rare:65 | ||||
chr11:32435537-32435765 | Common:1; Rare:57 | ||||
chr11:32829647-32829982 | Common:4; Rare:66 | ||||
chr11:33161443-33161565 | Common:4; Rare:32 | ||||
chr11:33257814-33257856 | Rare:11 |