Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:209675268-209675435 | Common:1; Rare:43 | ||||
chr1:209784514-209784704 | Rare:62 | ||||
chr1:209827838-209828123 | Common:1; Rare:77 | ||||
chr1:210328815-210328945 | Common:1; Rare:49 | ||||
chr1:211259008-211259408 | Common:1; Rare:125 | ||||
chr1:211259424-211259588 | Common:2; Rare:72 | ||||
chr1:211259733-211260011 | Rare:79 | ||||
chr1:211326718-211326872 | Common:3; Rare:39 | ||||
chr1:211675413-211675769 | Common:1; Rare:77; Clinvar (benign):1 | ||||
chr1:211830598-211830911 | Common:1; Rare:81 | ||||
chr1:212035488-212035834 | Common:2; Rare:96 | ||||
chr1:212432756-212433120 | Rare:96 | ||||
chr1:212608289-212608762 | Common:3; Rare:121 | ||||
chr1:212791707-212791972 | Common:6; Rare:127 | ||||
chr1:212858057-212858336 | Common:5; Rare:73; Clinvar:2 |