Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:188035625-188035737 | Rare:22 | ||||
chr2:193502478-193502794 | Common:9; Rare:103 | ||||
chr2:206812268-206812567 | Common:3; Rare:60 | ||||
chr2:231514337-231514579 | Common:5; Rare:95 | ||||
chr20:19758010-19758258 | Common:4; Rare:88 | ||||
chr20:40269140-40269406 | Common:8; Rare:67 | ||||
chr22:25448001-25448141 | Common:3; Rare:51 | ||||
chr22:30969044-30969278 | Common:2; Rare:66 | ||||
chr3:40453169-40453417 | Common:5; Rare:54 | ||||
chr3:54637895-54637986 | Common:1; Rare:26 | ||||
chr3:75435064-75435336 | Common:3; Rare:100 | ||||
chr3:143797516-143797850 | Common:2; Rare:72 | ||||
chr3:148414294-148414631 | Common:3; Rare:93 | ||||
chr3:169765053-169765258 | Rare:77; Clinvar (pathogenic):2 | ||||
chr3:175822831-175823088 | Common:1; Rare:54 |