Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:21345459-21345677 | Common:2; Rare:82 | ||||
chr1:21782985-21783318 | Common:3; Rare:125 | ||||
chr1:22451689-22451889 | Common:1; Rare:65 | ||||
chr1:23368841-23368965 | Common:1; Rare:42 | ||||
chr1:23530842-23531005 | Common:1; Rare:37 | ||||
chr1:23559416-23559684 | Common:2; Rare:114 | ||||
chr1:23691724-23691867 | Common:3; Rare:65; Clinvar:2; Clinvar (benign):2 | ||||
chr1:23743268-23743518 | Rare:93 | ||||
chr1:23778257-23778488 | Common:9; Rare:121 | ||||
chr1:23791065-23791225 | Rare:51 | ||||
chr1:23800729-23800965 | Common:1; Rare:86 | ||||
chr1:23825411-23825543 | Common:2; Rare:43; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:23959035-23959322 | Common:3; Rare:55 | ||||
chr1:23959641-23959854 | Common:2; Rare:57 | ||||
chr1:23979933-23980058 | Common:2; Rare:36 |