Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:140511239-140511449 | Common:3; Rare:87 | ||||
chr8:141391888-141392057 | Common:1; Rare:60 | ||||
chr8:142727040-142727274 | Common:3; Rare:95 | ||||
chr8:143018429-143018569 | Common:1; Rare:39 | ||||
chr8:143558262-143558419 | Common:1; Rare:64 | ||||
chr8:143684366-143684519 | Common:4; Rare:35 | ||||
chr8:143829026-143829129 | Rare:37 | ||||
chr8:143829296-143829486 | Rare:70 | ||||
chr8:144082484-144082685 | Common:2; Rare:67 | ||||
chr8:144103678-144103866 | Common:1; Rare:67 | ||||
chr8:144104222-144104496 | Common:1; Rare:81 | ||||
chr8:144291366-144291615 | Common:1; Rare:77 | ||||
chr8:144428493-144428658 | Common:2; Rare:63 | ||||
chr8:144509012-144509115 | Rare:31 | ||||
chr8:144517649-144518029 | Common:1; Rare:134; Clinvar:10; Clinvar (benign):2 |