Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:111605943-111606019 | Common:1; Rare:14 | ||||
chr6:111759546-111759753 | Common:2; Rare:40 | ||||
chr6:112087452-112087678 | Rare:68 | ||||
chr6:112139269-112139575 | Common:2; Rare:53; Clinvar:1; Clinvar (benign):1 | ||||
chr6:116100695-116100903 | Common:1; Rare:76 | ||||
chr6:116254046-116254251 | Common:4; Rare:58 | ||||
chr6:116279328-116279543 | Common:1; Rare:88 | ||||
chr6:116279850-116280092 | Common:1; Rare:83 | ||||
chr6:116370573-116370751 | Common:1; Rare:31 | ||||
chr6:116571209-116571595 | Common:3; Rare:108 | ||||
chr6:116681094-116681281 | Common:4; Rare:50 | ||||
chr6:118548157-118548367 | Common:2; Rare:45; Clinvar:3; Clinvar (benign):2 | ||||
chr6:118893947-118894302 | Common:2; Rare:102 | ||||
chr6:118934978-118935270 | Common:7; Rare:100 | ||||
chr6:119349732-119349936 | Common:3; Rare:73 |