Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:139198284-139198531 | Rare:83; Clinvar (benign):1 | ||||
chr5:139561733-139561793 | Rare:27 | ||||
chr5:140557427-140557536 | Common:1; Rare:66 | ||||
chr5:140564573-140564837 | Rare:73 | ||||
chr5:140647589-140647890 | Common:5; Rare:122; Clinvar:4; Clinvar (benign):3 | ||||
chr5:140664747-140664905 | Common:2; Rare:39 | ||||
chr5:140691313-140691515 | Common:1; Rare:77; Clinvar:7 | ||||
chr5:141320732-141320912 | Common:2; Rare:61 | ||||
chr5:141636810-141637001 | Common:2; Rare:83 | ||||
chr5:142108718-142108943 | Common:2; Rare:76 | ||||
chr5:142325019-142325236 | Rare:66 | ||||
chr5:148383740-148384054 | Rare:84 | ||||
chr5:149345344-149345536 | Common:1; Rare:65 | ||||
chr5:149551301-149551624 | Common:1; Rare:75 | ||||
chr5:149960569-149960773 | Rare:65; Clinvar:3 |