Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:143281672-143281817 | Common:1; Rare:29 | ||||
chr8:143579748-143580034 | Rare:102; Clinvar:1 | ||||
chr8:143583148-143583211 | Rare:12 | ||||
chr8:143653970-143654156 | Common:3; Rare:48 | ||||
chr8:143795131-143795280 | Rare:55 | ||||
chr8:143810520-143810712 | Common:1; Rare:91 | ||||
chr8:143820664-143820967 | Rare:74 | ||||
chr8:143828122-143828398 | Common:2; Rare:61 | ||||
chr8:143929803-143929988 | Common:1; Rare:96; Clinvar:8; Clinvar (benign):4 | ||||
chr8:143931474-143931581 | Common:2; Rare:38; Clinvar:2; Clinvar (benign):3 | ||||
chr8:143935092-143935289 | Common:1; Rare:73; Clinvar:5; Clinvar (benign):5 | ||||
chr8:143937030-143937258 | Common:2; Rare:83; Clinvar:7; Clinvar (benign):4 | ||||
chr8:143951789-143951948 | Common:1; Rare:41 | ||||
chr8:144427881-144427981 | Common:1; Rare:22 | ||||
chr8:144431102-144431381 | Common:2; Rare:65 |