Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:100266689-100266753 | Rare:9 | ||||
chr1:100266759-100266877 | Common:1; Rare:25 | ||||
chr1:100351292-100351457 | Rare:37 | ||||
chr1:100351606-100351827 | Common:2; Rare:73 | ||||
chr1:100352145-100352727 | Common:2; Rare:126 | ||||
chr1:100352827-100352979 | Common:1; Rare:52; Clinvar (benign):2 | ||||
chr1:100719609-100719769 | Common:1; Rare:41 | ||||
chr1:100894623-100894946 | Common:2; Rare:74 | ||||
chr1:100895682-100895775 | Rare:22 | ||||
chr1:100895792-100896282 | Common:1; Rare:142 | ||||
chr1:100896709-100896842 | Common:1; Rare:25 | ||||
chr1:101025314-101025377 | Rare:27 | ||||
chr1:101025696-101026016 | Common:2; Rare:88 | ||||
chr1:101236403-101236432 | Rare:4 | ||||
chr1:101236600-101237059 | Common:5; Rare:94 |