Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:832881-833014 | Common:7; Rare:49 | ||||
chr11:842464-842967 | Common:8; Rare:210 | ||||
chr11:844020-844153 | Common:1; Rare:32 | ||||
chr11:1309554-1309829 | Common:2; Rare:118 | ||||
chr11:2138346-2138585 | Common:2; Rare:60 | ||||
chr11:3057352-3057545 | Rare:69 | ||||
chr11:3797494-3797855 | Rare:124 | ||||
chr11:3808518-3808560 | Rare:14 | ||||
chr11:3840905-3841256 | Common:1; Rare:124 | ||||
chr11:3855551-3855711 | Common:2; Rare:32 | ||||
chr11:4393643-4393779 | Rare:31 | ||||
chr11:6390237-6390474 | Common:2; Rare:68 | ||||
chr11:6473889-6474124 | Rare:71 | ||||
chr11:6481292-6481524 | Common:4; Rare:92 | ||||
chr11:6603539-6603831 | Common:4; Rare:89; Clinvar (benign):3 |