Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:102918719-102918825 | Common:1; Rare:20; Clinvar (benign):1 | ||||
chr10:103192561-103193048 | Common:5; Rare:151 | ||||
chr10:103193050-103193090 | Rare:11 | ||||
chr10:103193127-103193452 | Common:5; Rare:99; Clinvar (benign):1 | ||||
chr10:103350490-103350658 | Rare:51 | ||||
chr10:103350757-103351253 | Common:2; Rare:194 | ||||
chr10:103367800-103368038 | Common:3; Rare:62 | ||||
chr10:103368254-103368309 | Rare:18 | ||||
chr10:103395864-103396121 | Common:2; Rare:52 | ||||
chr10:103396367-103396782 | Rare:139 | ||||
chr10:103451263-103451455 | Rare:38 | ||||
chr10:103452391-103452469 | Rare:19 | ||||
chr10:103855313-103855650 | Common:1; Rare:88 | ||||
chr10:103900484-103900531 | Rare:10 | ||||
chr10:103917791-103917987 | Rare:46 |