Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:101588211-101588339 | Rare:51 | ||||
chr10:101783379-101783479 | Rare:38 | ||||
chr10:101818376-101818770 | Common:1; Rare:103 | ||||
chr10:102114958-102115061 | Common:1; Rare:35 | ||||
chr10:102432533-102432797 | Common:1; Rare:77 | ||||
chr10:102714197-102714655 | Common:2; Rare:150 | ||||
chr10:102854193-102854284 | Rare:35 | ||||
chr10:103193250-103193527 | Common:4; Rare:80 | ||||
chr10:103350930-103351186 | Common:2; Rare:105 | ||||
chr10:103396411-103396699 | Rare:103 | ||||
chr10:104338446-104338594 | Rare:35 | ||||
chr10:109923425-109923638 | Common:2; Rare:79 | ||||
chr10:110007725-110008016 | Rare:81 | ||||
chr10:110567381-110567776 | Common:2; Rare:111; Clinvar:2; Clinvar (benign):5 | ||||
chr10:110919141-110919309 | Common:1; Rare:43 |