Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:104039069-104039371 | Common:1; Rare:71; Clinvar (benign):1 | ||||
chr10:109996873-109996898 | Rare:6 | ||||
chr10:110211171-110211392 | Common:1; Rare:53 | ||||
chr10:110872591-110872841 | Common:3; Rare:74 | ||||
chr10:110901579-110901906 | Common:1; Rare:68 | ||||
chr10:112372203-112372397 | Common:1; Rare:46 | ||||
chr10:112402026-112402034 | Common:1; Rare:1 | ||||
chr10:112426491-112426864 | Rare:77 | ||||
chr10:112951565-112951850 | Common:1; Rare:84 | ||||
chr10:112952002-112952057 | Common:1; Rare:20 | ||||
chr10:113063719-113063885 | Rare:30 | ||||
chr10:113161763-113161886 | Rare:28 | ||||
chr10:116624040-116624075 | Common:1; Rare:16 | ||||
chr10:116631296-116631352 | Rare:23 | ||||
chr10:122113721-122113775 | Rare:14 |