Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:95414935-95415099 | Rare:29 | ||||
chr10:103661666-103661867 | Common:1; Rare:59 | ||||
chr10:110764401-110764709 | Common:1; Rare:57 | ||||
chr10:114043117-114043259 | Rare:31 | ||||
chr10:114768080-114768372 | Common:1; Rare:67 | ||||
chr10:119036244-119036460 | Rare:39 | ||||
chr10:124703889-124704097 | Rare:31 | ||||
chr10:132518188-132518379 | Rare:30 | ||||
chr11:1995901-1996253 | Common:3; Rare:115 | ||||
chr11:2138317-2138392 | Common:1; Rare:22 | ||||
chr11:9758160-9758320 | Rare:44 | ||||
chr11:14759382-14759597 | Common:2; Rare:46 | ||||
chr11:20049158-20049248 | Rare:23 | ||||
chr11:20049306-20049535 | Rare:29 | ||||
chr11:47337389-47337795 | Common:3; Rare:141; Clinvar:24; Clinvar (benign):16; Clinvar (pathogenic):16 |