Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:959193-959452 | Common:1; Rare:136 | ||||
chr1:960509-960671 | Rare:44 | ||||
chr1:966900-967049 | Common:1; Rare:62 | ||||
chr1:1000065-1000548 | Common:8; Rare:159 | ||||
chr1:1013275-1013571 | Common:6; Rare:94 | ||||
chr1:1019901-1020187 | Common:2; Rare:91; Clinvar:1; Clinvar (benign):1 | ||||
chr1:1020261-1020332 | Rare:19 | ||||
chr1:1212990-1213166 | Common:1; Rare:74; Clinvar (benign):2 | ||||
chr1:1231883-1232368 | Rare:174; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
chr1:1273776-1274257 | Common:5; Rare:166 | ||||
chr1:1305442-1305549 | Rare:23 | ||||
chr1:1305652-1305860 | Rare:70 | ||||
chr1:1307831-1308227 | Common:1; Rare:102 | ||||
chr1:1308312-1308693 | Common:9; Rare:161 | ||||
chr1:1324330-1324455 | Rare:37 |