Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:243473183-243473408 | Common:2; Rare:26 | ||||
chr1:244047820-244047837 | Rare:3 | ||||
chr1:244049661-244049982 | Rare:86 | ||||
chr1:244052139-244052542 | Common:1; Rare:72 | ||||
chr1:244053122-244053370 | Common:3; Rare:42 | ||||
chr1:244863702-244863788 | Rare:26; Clinvar (benign):1 | ||||
chr1:244863816-244863875 | Rare:19; Clinvar:1 | ||||
chr10:6163657-6163880 | Common:6; Rare:79 | ||||
chr10:10294274-10294304 | Rare:2 | ||||
chr10:10294654-10294786 | Common:1; Rare:29 | ||||
chr10:10462229-10462570 | Common:3; Rare:80 | ||||
chr10:10465650-10465681 | Rare:7 | ||||
chr10:10798334-10798380 | Rare:12 | ||||
chr10:10798705-10798767 | Rare:18 | ||||
chr10:11003712-11004052 | Rare:65 |