Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:40691503-40691867 | Common:2; Rare:161 | ||||
chr1:40691959-40692030 | Common:1; Rare:23 | ||||
chr1:40692033-40692111 | Rare:31 | ||||
chr1:40709160-40709413 | Rare:58 | ||||
chr1:40979627-40979797 | Common:1; Rare:61 | ||||
chr1:41242089-41242449 | Common:1; Rare:103 | ||||
chr1:42335099-42335434 | Common:6; Rare:158 | ||||
chr1:42455993-42456108 | Rare:40 | ||||
chr1:42456446-42456621 | Common:1; Rare:79 | ||||
chr1:42658271-42658512 | Common:2; Rare:74 | ||||
chr1:42682132-42682488 | Common:2; Rare:102 | ||||
chr1:42682515-42682751 | Common:1; Rare:83 | ||||
chr1:42683265-42683465 | Common:3; Rare:80 | ||||
chr1:42766952-42767324 | Common:5; Rare:129; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr1:42816986-42817146 | Common:1; Rare:43 |