Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:24642983-24643351 | Common:2; Rare:111 | ||||
chr1:24745309-24745613 | Common:2; Rare:106 | ||||
chr1:25232460-25232654 | Rare:75 | ||||
chr1:26021630-26021789 | Common:1; Rare:25 | ||||
chr1:26279934-26280206 | Rare:145 | ||||
chr1:26432095-26432418 | Common:5; Rare:87; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26695928-26696062 | Rare:43 | ||||
chr1:26900408-26900526 | Rare:50 | ||||
chr1:28505803-28506135 | Common:4; Rare:138 | ||||
chr1:28643018-28643184 | Rare:65 | ||||
chr1:28736719-28737019 | Common:2; Rare:99 | ||||
chr1:29123891-29124011 | Common:1; Rare:49 | ||||
chr1:31296730-31297139 | Common:5; Rare:124 | ||||
chr1:31578013-31578203 | Rare:25 | ||||
chr1:31703898-31704055 | Common:2; Rare:37 |