Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:206635416-206635604 | Common:1; Rare:52 | ||||
chr1:206684783-206684964 | Rare:60 | ||||
chr1:206685304-206685425 | Common:1; Rare:34 | ||||
chr1:206865372-206865676 | Rare:44 | ||||
chr1:206909503-206909685 | Common:3; Rare:44 | ||||
chr1:207032606-207033040 | Common:5; Rare:72 | ||||
chr1:207050941-207051145 | Common:1; Rare:90 | ||||
chr1:207053091-207053376 | Common:1; Rare:73 | ||||
chr1:207752027-207752272 | Common:1; Rare:77; Clinvar:1 | ||||
chr1:209651129-209651397 | Common:2; Rare:50 | ||||
chr1:209652248-209652643 | Common:3; Rare:80; Clinvar:2; Clinvar (benign):1 | ||||
chr1:209652805-209653164 | Common:2; Rare:60 | ||||
chr1:209675263-209675480 | Common:1; Rare:53 | ||||
chr1:209784407-209784618 | Rare:64 | ||||
chr1:209802230-209802407 | Rare:22 |