Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:122954174-122954484 | Rare:111 | ||||
chr10:123008791-123009021 | Common:5; Rare:62; Clinvar:4; Clinvar (benign):5 | ||||
chr10:124801645-124801827 | Rare:55 | ||||
chr10:125719462-125719742 | Common:1; Rare:95 | ||||
chr10:125823200-125823594 | Common:1; Rare:139; Clinvar:1; Clinvar (benign):1 | ||||
chr10:126905308-126905458 | Rare:57 | ||||
chr10:132331794-132332213 | Common:16; Rare:140 | ||||
chr10:133308835-133308982 | Rare:69 | ||||
chr11:207372-207749 | Common:8; Rare:113 | ||||
chr11:208662-208847 | Rare:70 | ||||
chr11:236333-236513 | Common:6; Rare:52 | ||||
chr11:236913-237047 | Common:1; Rare:53 | ||||
chr11:507169-507476 | Common:4; Rare:100 | ||||
chr11:560689-561003 | Common:6; Rare:149 | ||||
chr11:576413-576519 | Rare:43 |