Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:101062040-101063507 | Common:23; Rare:1236 | ||||
chr10:101066094-101066494 | Common:3; Rare:270 | ||||
chr10:101066500-101066870 | Common:6; Rare:178 | ||||
chr10:101131019-101131425 | Common:4; Rare:231 | ||||
chr10:101353651-101354222 | Common:3; Rare:390 | ||||
chr10:101570212-101570612 | Common:3; Rare:176 | ||||
chr10:101588082-101588482 | Common:1; Rare:632; Clinvar:2 | ||||
chr10:101694360-101694938 | Common:14; Rare:416; Clinvar:18; Clinvar (benign):17 | ||||
chr10:101694941-101695341 | Rare:143; Clinvar:1 | ||||
chr10:101783261-101784123 | Common:8; Rare:547 | ||||
chr10:101816821-101818371 | Common:10; Rare:716 | ||||
chr10:101818284-101819324 | Common:9; Rare:917 | ||||
chr10:101829559-101829959 | Rare:128 | ||||
chr10:101830370-101830870 | Common:7; Rare:127 | ||||
chr10:101830928-101831087 | Common:1; Rare:41 |