Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:40691590-40691864 | Common:1; Rare:120 | ||||
chr1:40692033-40692421 | Common:2; Rare:111 | ||||
chr1:40979631-40979766 | Common:1; Rare:49 | ||||
chr1:41242104-41242399 | Rare:88 | ||||
chr1:42335129-42335346 | Common:4; Rare:115 | ||||
chr1:42455993-42456595 | Common:1; Rare:185 | ||||
chr1:42463015-42463344 | Common:4; Rare:102 | ||||
chr1:42658273-42658534 | Common:2; Rare:76 | ||||
chr1:42682132-42682465 | Common:2; Rare:91 | ||||
chr1:42682605-42682731 | Common:1; Rare:52 | ||||
chr1:42683185-42683466 | Common:3; Rare:128 | ||||
chr1:42766978-42767312 | Common:4; Rare:115; Clinvar (benign):1 | ||||
chr1:42816981-42817138 | Common:1; Rare:45 | ||||
chr1:42817219-42817385 | Rare:74 | ||||
chr1:42846399-42846657 | Common:1; Rare:75 |