Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:183659122-183659401 | Common:1; Rare:93 | ||||
chr4:184474484-184474810 | Rare:71 | ||||
chr4:184649403-184649781 | Common:4; Rare:126 | ||||
chr4:184734052-184734403 | Common:5; Rare:126 | ||||
chr4:184805664-184805832 | Common:1; Rare:26 | ||||
chr4:185143105-185143290 | Common:3; Rare:57; Clinvar (benign):3 | ||||
chr4:185425880-185426242 | Common:3; Rare:108 | ||||
chr4:185535488-185535640 | Rare:40 | ||||
chr4:186723708-186723952 | Common:5; Rare:99 | ||||
chr4:186726367-186726751 | Common:5; Rare:96 | ||||
chr4:189940613-189941030 | Common:16; Rare:151 | ||||
chr5:218106-218376 | Common:4; Rare:115; Clinvar:8; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
chr5:612211-612351 | Rare:55 | ||||
chr5:892699-892927 | Common:5; Rare:84 | ||||
chr5:1799795-1799986 | Common:4; Rare:91 |