Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:230642637-230642841 | Common:1; Rare:84 | ||||
chr1:230642896-230643007 | Rare:22 | ||||
chr1:230868258-230868383 | Rare:43 | ||||
chr1:230868412-230868710 | Common:1; Rare:86 | ||||
chr1:230868813-230868901 | Rare:18 | ||||
chr1:230869007-230869077 | Common:1; Rare:13 | ||||
chr1:230978322-230978441 | Rare:34 | ||||
chr1:230978699-230979325 | Common:4; Rare:232; Clinvar (benign):1 | ||||
chr1:231039812-231039894 | Common:2; Rare:23 | ||||
chr1:231040145-231040394 | Common:1; Rare:96 | ||||
chr1:231240422-231240954 | Common:4; Rare:86 | ||||
chr1:231241032-231241384 | Common:3; Rare:169; Clinvar:5; Clinvar (benign):2 | ||||
chr1:231241398-231241508 | Common:1; Rare:43; Clinvar:1; Clinvar (benign):1 | ||||
chr1:231337418-231337639 | Common:1; Rare:57 | ||||
chr1:231337762-231338134 | Common:5; Rare:132 |