Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:86396044-86396111 | Rare:18 | ||||
chr1:86396277-86396410 | Common:1; Rare:31 | ||||
chr1:86914325-86914632 | Common:1; Rare:78 | ||||
chr1:88683962-88684350 | Common:3; Rare:115 | ||||
chr1:89994979-89995157 | Common:2; Rare:72 | ||||
chr1:91021998-91022156 | Rare:49 | ||||
chr1:92298944-92299070 | Common:1; Rare:59; Clinvar:1; Clinvar (benign):1 | ||||
chr1:92785082-92785406 | Common:6; Rare:102 | ||||
chr1:93079067-93079290 | Common:3; Rare:97 | ||||
chr1:93180298-93180736 | Common:1; Rare:175 | ||||
chr1:93345807-93345919 | Common:2; Rare:43 | ||||
chr1:93448002-93448213 | Common:2; Rare:72 | ||||
chr1:93879144-93879273 | Common:1; Rare:43 | ||||
chr1:94418117-94418464 | Common:2; Rare:123 | ||||
chr1:94541751-94541982 | Rare:70 |