Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:68817590-68817684 | Rare:28 | ||||
chr15:69160333-69160658 | Common:4; Rare:100 | ||||
chr15:69414209-69414372 | Rare:46 | ||||
chr15:69452774-69453020 | Common:5; Rare:109 | ||||
chr15:70095230-70095357 | Common:1; Rare:32 | ||||
chr15:70097814-70098085 | Common:5; Rare:66 | ||||
chr15:70763328-70763735 | Common:2; Rare:135 | ||||
chr15:70854119-70854289 | Rare:56 | ||||
chr15:70892555-70892684 | Common:1; Rare:23 | ||||
chr15:71547221-71547346 | Rare:32 | ||||
chr15:72118055-72118417 | Common:3; Rare:119 | ||||
chr15:72231117-72231266 | Rare:58 | ||||
chr15:72272201-72272242 | Rare:7 | ||||
chr15:72375657-72375771 | Rare:25; Clinvar:1; Clinvar (pathogenic):3 | ||||
chr15:72375935-72376144 | Common:3; Rare:83; Clinvar:7; Clinvar (benign):2; Clinvar (pathogenic):5 |