Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:22982515-22982726 | Rare:80 | ||||
chr14:23095108-23095441 | Common:1; Rare:155 | ||||
chr14:23095446-23095587 | Common:2; Rare:57 | ||||
chr14:23306639-23306867 | Common:1; Rare:52 | ||||
chr14:23567756-23567913 | Rare:32 | ||||
chr14:23953611-23953810 | Common:8; Rare:80 | ||||
chr14:24094019-24094323 | Common:3; Rare:75 | ||||
chr14:24115018-24115280 | Common:2; Rare:72 | ||||
chr14:24141588-24141862 | Rare:56 | ||||
chr14:24146563-24146881 | Common:1; Rare:100 | ||||
chr14:24195410-24195715 | Common:1; Rare:69 | ||||
chr14:24213425-24213598 | Common:1; Rare:58 | ||||
chr14:24232312-24232663 | Common:8; Rare:83 | ||||
chr14:24232848-24232929 | Rare:20 | ||||
chr14:24242295-24242507 | Rare:63; Clinvar (benign):3 |