Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:230978158-230978229 | Common:2; Rare:22 | ||||
chr1:231211438-231211705 | Common:1; Rare:72 | ||||
chr1:231421225-231421297 | Rare:20; Clinvar (benign):1 | ||||
chr1:231422163-231422569 | Common:6; Rare:180; Clinvar:6; Clinvar (benign):6 | ||||
chr1:231422617-231422777 | Rare:40; Clinvar:1; Clinvar (benign):1 | ||||
chr1:231612772-231612886 | Common:1; Rare:19 | ||||
chr1:232630100-232630264 | Rare:62 | ||||
chr1:233673499-233673680 | Common:2; Rare:30 | ||||
chr1:233673807-233673986 | Rare:35 | ||||
chr1:234216414-234216435 | Rare:3 | ||||
chr1:234399245-234399266 | Rare:4 | ||||
chr1:234473283-234473354 | Rare:15 | ||||
chr1:234478149-234478421 | Common:2; Rare:119 | ||||
chr1:234495283-234495528 | Common:4; Rare:40 | ||||
chr1:234495619-234495792 | Common:1; Rare:30 |