Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:179025696-179026188 | Common:12; Rare:186 | ||||
chr1:179026190-179026351 | Rare:53 | ||||
chr1:179081856-179082160 | Common:2; Rare:166 | ||||
chr1:179143052-179143258 | Rare:73 | ||||
chr1:179229539-179229862 | Common:11; Rare:108 | ||||
chr1:179229880-179230270 | Common:4; Rare:147 | ||||
chr1:179293572-179293933 | Common:6; Rare:220 | ||||
chr1:179365530-179366164 | Common:52; Rare:403 | ||||
chr1:179877747-179877898 | Rare:62 | ||||
chr1:179882129-179882343 | Common:2; Rare:70 | ||||
chr1:179882481-179882874 | Rare:363; Clinvar:15; Clinvar (benign):4 | ||||
chr1:179883012-179883160 | Common:3; Rare:57 | ||||
chr1:179954641-179954830 | Common:2; Rare:78 | ||||
chr1:180154665-180154923 | Common:5; Rare:177 | ||||
chr1:180229876-180230310 | Common:9; Rare:253 |