Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:244863796-244863875 | Rare:26; Clinvar:1; Clinvar (benign):1 | ||||
chr1:244970924-244971132 | Common:1; Rare:65 | ||||
chr1:246569745-246569899 | Common:1; Rare:29 | ||||
chr10:241936-242132 | Rare:54 | ||||
chr10:247160-247463 | Rare:56 | ||||
chr10:3783007-3783118 | Rare:30 | ||||
chr10:3783424-3783574 | Rare:34 | ||||
chr10:3783882-3784042 | Common:3; Rare:42 | ||||
chr10:3853585-3853917 | Common:2; Rare:64 | ||||
chr10:3861064-3861368 | Common:8; Rare:61 | ||||
chr10:3911946-3912090 | Common:1; Rare:35 | ||||
chr10:4243666-4243912 | Common:1; Rare:50 | ||||
chr10:4941757-4941910 | Rare:43 | ||||
chr10:5712557-5712889 | Common:2; Rare:61 | ||||
chr10:5766494-5766769 | Common:1; Rare:63 |