Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:6619409-6619570 | Common:2; Rare:47; Clinvar:1; Clinvar (benign):5 | ||||
chr11:6926316-6926562 | Common:5; Rare:68 | ||||
chr11:7020312-7020502 | Rare:68 | ||||
chr11:7513626-7513937 | Common:5; Rare:89 | ||||
chr11:8168991-8169048 | Rare:22 | ||||
chr11:8594163-8594322 | Rare:55 | ||||
chr11:8682638-8682816 | Common:2; Rare:79 | ||||
chr11:8910921-8911295 | Common:7; Rare:108 | ||||
chr11:8964417-8964513 | Common:3; Rare:27 | ||||
chr11:9003996-9004142 | Rare:50 | ||||
chr11:9460607-9461051 | Common:4; Rare:114 | ||||
chr11:9664013-9664191 | Common:4; Rare:69 | ||||
chr11:10304915-10305078 | Common:1; Rare:33 | ||||
chr11:10541145-10541314 | Rare:65 | ||||
chr11:10751174-10751279 | Rare:32 |