Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:99969878-99970106 | Rare:55 | ||||
chr1:100038006-100038193 | Common:1; Rare:76 | ||||
chr1:100132895-100133260 | Common:2; Rare:144 | ||||
chr1:100249796-100250017 | Common:3; Rare:77; Clinvar:1; Clinvar (benign):1 | ||||
chr1:100266107-100266331 | Common:3; Rare:82 | ||||
chr1:100894633-100895014 | Common:2; Rare:89 | ||||
chr1:100895987-100896155 | Rare:46 | ||||
chr1:101025763-101025916 | Common:1; Rare:45 | ||||
chr1:101236611-101237042 | Common:5; Rare:84 | ||||
chr1:103525502-103525774 | Rare:70 | ||||
chr1:103525908-103526221 | Common:1; Rare:97 | ||||
chr1:107056467-107056781 | Common:2; Rare:124 | ||||
chr1:107140190-107140353 | Common:1; Rare:33 | ||||
chr1:107688415-107688724 | Rare:52 | ||||
chr1:108200120-108200450 | Common:9; Rare:104 |