Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:47380806-47381090 | Rare:96 | ||||
chr3:47475803-47476058 | Common:3; Rare:105 | ||||
chr3:48240991-48241183 | Common:3; Rare:65 | ||||
chr3:48301325-48301612 | Common:3; Rare:91 | ||||
chr3:48440056-48440309 | Common:1; Rare:97 | ||||
chr3:48446652-48446766 | Common:1; Rare:40 | ||||
chr3:48847624-48847965 | Common:1; Rare:94 | ||||
chr3:48918794-48918949 | Common:2; Rare:90 | ||||
chr3:49007201-49007432 | Common:2; Rare:90 | ||||
chr3:49021503-49021732 | Rare:55; Clinvar:1 | ||||
chr3:49028305-49028491 | Rare:58 | ||||
chr3:49029346-49029536 | Common:2; Rare:134 | ||||
chr3:49104722-49104930 | Rare:87; Clinvar (benign):4 | ||||
chr3:49120747-49121117 | Rare:103 | ||||
chr3:49132836-49133143 | Rare:70; Clinvar:3 |