Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:100987256-100987639 | Common:2; Rare:131; Clinvar:1; Clinvar (benign):2 | ||||
chr10:100999726-100999934 | Common:1; Rare:64 | ||||
chr10:101031102-101031311 | Common:1; Rare:46 | ||||
chr10:101038002-101038202 | Common:1; Rare:22 | ||||
chr10:101061714-101062007 | Rare:48 | ||||
chr10:101587847-101587911 | Rare:20 | ||||
chr10:101588101-101588333 | Rare:102 | ||||
chr10:101783315-101783522 | Rare:90 | ||||
chr10:101793216-101793305 | Rare:18 | ||||
chr10:101793320-101793542 | Rare:41 | ||||
chr10:101817825-101817978 | Common:3; Rare:53 | ||||
chr10:101818342-101818557 | Rare:69 | ||||
chr10:102065341-102065472 | Rare:48 | ||||
chr10:102120456-102120560 | Common:1; Rare:37 | ||||
chr10:102132846-102133077 | Common:1; Rare:57 |