Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:74171783-74172027 | Rare:43 | ||||
chr11:74230759-74230974 | Rare:34 | ||||
chr11:74231264-74231392 | Common:1; Rare:21 | ||||
chr11:74398381-74398525 | Common:3; Rare:27 | ||||
chr11:74949061-74949352 | Common:6; Rare:87 | ||||
chr11:74988662-74988703 | Rare:8 | ||||
chr11:74988810-74988957 | Rare:37 | ||||
chr11:75351651-75351916 | Common:3; Rare:78 | ||||
chr11:75562053-75562413 | Common:1; Rare:78; Clinvar:4; Clinvar (benign):2 | ||||
chr11:75562690-75562926 | Common:1; Rare:47 | ||||
chr11:76783023-76783366 | Common:9; Rare:115 | ||||
chr11:77066952-77067085 | Common:1; Rare:39 | ||||
chr11:77590124-77590326 | Common:2; Rare:58 | ||||
chr11:77637591-77637725 | Rare:36 | ||||
chr11:77637742-77637823 | Rare:38 |