Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:222589871-222590074 | Common:2; Rare:53 | ||||
chr1:222644137-222644351 | Common:1; Rare:60 | ||||
chr1:222712437-222712599 | Rare:54 | ||||
chr1:222713243-222713404 | Common:1; Rare:49 | ||||
chr1:223712287-223712636 | Common:2; Rare:108 | ||||
chr1:224183040-224183289 | Common:3; Rare:105 | ||||
chr1:224330159-224330471 | Common:5; Rare:101 | ||||
chr1:225428026-225428352 | Common:3; Rare:104; Clinvar:2; Clinvar (benign):2 | ||||
chr1:225924136-225924453 | Common:8; Rare:102 | ||||
chr1:225999316-225999616 | Common:2; Rare:100 | ||||
chr1:226062081-226062094 | Rare:2 | ||||
chr1:226062668-226062784 | Rare:49 | ||||
chr1:226186714-226186789 | Rare:22 | ||||
chr1:226309135-226309415 | Common:1; Rare:123 | ||||
chr1:226407943-226408321 | Common:4; Rare:114 |