Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:156741378-156742254 | Common:12; Rare:335 | ||||
chr1:156747060-156747776 | Common:10; Rare:202 | ||||
chr1:156750188-156752524 | Common:28; Rare:1959 | ||||
chr1:156766228-156766628 | Common:3; Rare:72 | ||||
chr1:156766970-156767620 | Common:9; Rare:727 | ||||
chr1:156767774-156768240 | Common:2; Rare:467 | ||||
chr1:156786301-156786846 | Common:1; Rare:139 | ||||
chr1:156813848-156814248 | Rare:372 | ||||
chr1:156816660-156817100 | Common:7; Rare:285 | ||||
chr1:156858557-156859700 | Common:20; Rare:680 | ||||
chr1:156860050-156860480 | Common:4; Rare:233 | ||||
chr1:156860500-156861060 | Common:16; Rare:511; Clinvar:6; Clinvar (benign):18; Clinvar (pathogenic):3 | ||||
chr1:156912940-156913872 | Common:33; Rare:842 | ||||
chr1:156920349-156920749 | Common:1; Rare:186 | ||||
chr1:156927672-156928251 | Common:2; Rare:200 |