Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:140924706-140925059 | Common:3; Rare:125; Clinvar:2; Clinvar (benign):5 | ||||
chr7:141551243-141551428 | Common:2; Rare:53; Clinvar:5; Clinvar (benign):2 | ||||
chr7:141738001-141738464 | Common:4; Rare:140 | ||||
chr7:143263398-143263532 | Rare:43 | ||||
chr7:143902122-143902292 | Common:5; Rare:55 | ||||
chr7:144836026-144836123 | Rare:30 | ||||
chr7:148884165-148884440 | Common:1; Rare:124; Clinvar:3; Clinvar (benign):1 | ||||
chr7:149028402-149028566 | Common:2; Rare:66 | ||||
chr7:149028586-149028938 | Common:5; Rare:119 | ||||
chr7:149090705-149090876 | Rare:45 | ||||
chr7:150368716-150368854 | Rare:44 | ||||
chr7:150379084-150379311 | Common:1; Rare:74 | ||||
chr7:151028155-151028466 | Rare:101 | ||||
chr7:151057876-151058149 | Common:3; Rare:72 | ||||
chr7:151232382-151232525 | Common:1; Rare:47 |