Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:75403655-75404044 | Common:1; Rare:107 | ||||
chr10:77925656-77925719 | Rare:11 | ||||
chr10:79826347-79826693 | Common:3; Rare:94 | ||||
chr10:79904782-79905044 | Common:4; Rare:63 | ||||
chr10:80467989-80468250 | Common:1; Rare:52 | ||||
chr10:86955672-86955785 | Rare:20 | ||||
chr10:86970916-86971105 | Common:3; Rare:39 | ||||
chr10:86971207-86971268 | Rare:18 | ||||
chr10:87342318-87342920 | Common:5; Rare:184 | ||||
chr10:87862252-87862570 | Rare:154; Clinvar:1 | ||||
chr10:88948800-88949254 | Rare:82; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
chr10:89283374-89283750 | Common:1; Rare:53 | ||||
chr10:91807506-91807607 | Rare:25 | ||||
chr10:92831026-92831158 | Rare:24 | ||||
chr10:93437093-93437405 | Common:4; Rare:67 |