Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:6419900-6419926 | Rare:5 | ||||
chr1:6424647-6424806 | Common:1; Rare:52 | ||||
chr1:6440416-6440696 | Common:11; Rare:80; Clinvar (benign):3 | ||||
chr1:6471528-6471799 | Common:1; Rare:91; Clinvar (benign):4 | ||||
chr1:6485464-6485510 | Rare:11 | ||||
chr1:6489934-6490110 | Common:1; Rare:32 | ||||
chr1:6490477-6490942 | Common:1; Rare:99 | ||||
chr1:6490988-6491022 | Rare:8 | ||||
chr1:6497414-6497656 | Common:2; Rare:69 | ||||
chr1:6554489-6554732 | Common:7; Rare:73 | ||||
chr1:6579556-6579661 | Rare:29 | ||||
chr1:6579772-6580098 | Common:5; Rare:105 | ||||
chr1:6602526-6602665 | Rare:64 | ||||
chr1:6602815-6603293 | Common:5; Rare:172 | ||||
chr1:6603451-6603858 | Common:2; Rare:94 |