Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:115641776-115642004 | Common:3; Rare:78; Clinvar:1; Clinvar (benign):2 | ||||
chr1:117929568-117929789 | Common:1; Rare:66 | ||||
chr1:119140648-119140761 | Rare:32 | ||||
chr1:145823937-145824238 | Rare:106 | ||||
chr1:145918700-145919013 | Common:2; Rare:64 | ||||
chr1:145927433-145927612 | Common:1; Rare:49; Clinvar (pathogenic):1 | ||||
chr1:149850902-149851064 | |||||
chr1:149886646-149887004 | Common:2; Rare:132 | ||||
chr1:149887908-149888195 | Rare:90 | ||||
chr1:150067595-150067844 | Common:1; Rare:68 | ||||
chr1:150236065-150236368 | Rare:64 | ||||
chr1:150282291-150282586 | Common:3; Rare:57 | ||||
chr1:150629568-150629825 | Rare:46 | ||||
chr1:151165851-151166158 | Common:3; Rare:86 | ||||
chr1:151198428-151198586 | Common:1; Rare:54 |