Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:6393264-6393651 | Common:5; Rare:134 | ||||
chr1:6393689-6394180 | Common:2; Rare:140 | ||||
chr1:6419848-6420021 | Common:2; Rare:52 | ||||
chr1:6424675-6424786 | Common:1; Rare:42 | ||||
chr1:6489929-6490181 | Common:1; Rare:43 | ||||
chr1:6490434-6490971 | Common:3; Rare:112; Clinvar (benign):1 | ||||
chr1:6490985-6491058 | Rare:13 | ||||
chr1:6491165-6491252 | Rare:14 | ||||
chr1:6491287-6491319 | Rare:11 | ||||
chr1:6491412-6491804 | Common:2; Rare:49; Clinvar (benign):1 | ||||
chr1:6497414-6497681 | Common:2; Rare:75 | ||||
chr1:6554412-6554659 | Common:6; Rare:90 | ||||
chr1:6579547-6579590 | Rare:9 | ||||
chr1:6579708-6580108 | Common:5; Rare:129 | ||||
chr1:6599935-6600251 | Common:1; Rare:92 |