Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:138501649-138502026 | Common:4; Rare:137 | ||||
chr2:144513779-144513954 | Rare:46 | ||||
chr2:144514918-144515019 | Rare:21 | ||||
chr2:144517426-144517610 | Rare:41 | ||||
chr2:144517628-144517691 | Rare:23 | ||||
chr2:144518134-144518203 | Common:1; Rare:14 | ||||
chr2:144518386-144518495 | Rare:25 | ||||
chr2:144520136-144520547 | Common:4; Rare:72; Clinvar (benign):1 | ||||
chr2:148020688-148021096 | Common:2; Rare:95; Clinvar (benign):2 | ||||
chr2:148021329-148021415 | Rare:16 | ||||
chr2:148021429-148021477 | Rare:10 | ||||
chr2:149587685-149587814 | Common:1; Rare:37; Clinvar:1 | ||||
chr2:151828459-151828619 | Common:2; Rare:42 | ||||
chr2:152175670-152176092 | Common:3; Rare:117 | ||||
chr2:152335008-152335174 | Common:1; Rare:60 |