Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:168038119-168038412 | Common:1; Rare:55 | ||||
chr1:168056493-168056626 | Common:1; Rare:22 | ||||
chr1:168239478-168239689 | Rare:27 | ||||
chr1:169129851-169130084 | Common:5; Rare:43; Clinvar (benign):1 | ||||
chr1:169160820-169161127 | Common:1; Rare:40 | ||||
chr1:169200959-169201126 | Common:2; Rare:32 | ||||
chr1:171558069-171558394 | Common:5; Rare:73 | ||||
chr1:171591146-171591485 | Common:2; Rare:56 | ||||
chr1:171743202-171743335 | Rare:20 | ||||
chr1:171824765-171824967 | Rare:45 | ||||
chr1:172040685-172040876 | Rare:43 | ||||
chr1:172181823-172182135 | Rare:56 | ||||
chr1:172482444-172482585 | Common:2; Rare:21 | ||||
chr1:172973480-172973741 | Common:1; Rare:55 | ||||
chr1:173351928-173352003 | Rare:8 |