Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:46693642-46693768 | Common:1; Rare:32 | ||||
chr3:46979504-46979871 | Common:3; Rare:96; Clinvar:2 | ||||
chr3:46981981-46982186 | Rare:32 | ||||
chr3:46995597-46995771 | Rare:55; Clinvar:2; Clinvar (pathogenic):1 | ||||
chr3:47163887-47164227 | Common:1; Rare:96; Clinvar (pathogenic):1 | ||||
chr3:47380822-47381072 | Rare:75 | ||||
chr3:47802879-47803199 | Common:1; Rare:96 | ||||
chr3:48088792-48089057 | Rare:87 | ||||
chr3:48089248-48089363 | Rare:34 | ||||
chr3:48301363-48301622 | Common:3; Rare:74 | ||||
chr3:48440035-48440316 | Common:1; Rare:106 | ||||
chr3:48847676-48847954 | Common:1; Rare:77 | ||||
chr3:48918804-48918903 | Common:2; Rare:56 | ||||
chr3:49007086-49007424 | Common:2; Rare:130 | ||||
chr3:49018552-49018605 | Rare:21 |