Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:71080978-71081383 | Rare:111 | ||||
chr1:72282669-72282979 | Common:4; Rare:92 | ||||
chr1:74198148-74198347 | Common:2; Rare:111 | ||||
chr1:74732994-74733363 | Common:6; Rare:130 | ||||
chr1:75724308-75724654 | Common:5; Rare:102; Clinvar:3; Clinvar (benign):4 | ||||
chr1:76074572-76074856 | Common:2; Rare:92 | ||||
chr1:77219385-77219525 | Rare:66 | ||||
chr1:77683322-77683556 | Common:1; Rare:75 | ||||
chr1:77888073-77888362 | Common:1; Rare:71 | ||||
chr1:77888369-77888758 | Common:2; Rare:88; Clinvar:2; Clinvar (benign):1 | ||||
chr1:77941847-77942203 | Rare:118; Clinvar:13; Clinvar (benign):5 | ||||
chr1:77947227-77947434 | Rare:33 | ||||
chr1:77979006-77979344 | Common:3; Rare:115 | ||||
chr1:77979407-77979550 | Common:1; Rare:36 | ||||
chr1:78004547-78005001 | Common:4; Rare:99 |