Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:75296184-75296415 | Common:1; Rare:43 | ||||
chr10:77925371-77925702 | Rare:53 | ||||
chr10:79067408-79067441 | Common:1; Rare:15 | ||||
chr10:79070010-79070151 | Rare:52 | ||||
chr10:79071090-79071418 | Common:1; Rare:80 | ||||
chr10:79148966-79149046 | Rare:10 | ||||
chr10:79309255-79309545 | Common:3; Rare:90 | ||||
chr10:79555803-79555919 | Rare:29 | ||||
chr10:79558540-79559028 | Common:17; Rare:173; Clinvar:1; Clinvar (benign):2 | ||||
chr10:79585915-79586063 | Common:1; Rare:37 | ||||
chr10:79612293-79612740 | Common:6; Rare:144; Clinvar (benign):2 | ||||
chr10:79613031-79613582 | Common:5; Rare:140; Clinvar (benign):1 | ||||
chr10:79826315-79826901 | Common:5; Rare:176 | ||||
chr10:79904534-79904925 | Common:2; Rare:96 | ||||
chr10:80166906-80167320 | Common:5; Rare:131 |