Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:231528575-231528820 | Common:2; Rare:84 | ||||
chr1:232950384-232950713 | Common:5; Rare:117 | ||||
chr1:233295712-233295802 | Common:1; Rare:27 | ||||
chr1:234373282-234373775 | Common:1; Rare:214; Clinvar (benign):7 | ||||
chr1:234608173-234608428 | Common:1; Rare:92 | ||||
chr1:235128592-235128991 | Rare:158 | ||||
chr1:235160891-235161342 | Common:3; Rare:218 | ||||
chr1:235328015-235328636 | Common:4; Rare:187 | ||||
chr1:235328816-235329008 | Common:1; Rare:59 | ||||
chr1:235504385-235504748 | Common:5; Rare:116 | ||||
chr1:235866852-235867124 | Common:3; Rare:79 | ||||
chr1:235883702-235883912 | Rare:37 | ||||
chr1:236064887-236064974 | Rare:27 | ||||
chr1:236065053-236065246 | Rare:82; Clinvar (pathogenic):1 | ||||
chr1:236142933-236142937 |