Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:155185406-155185540 | Rare:28 | ||||
chr1:155186323-155186536 | Common:1; Rare:36 | ||||
chr1:155194699-155194827 | Common:1; Rare:42 | ||||
chr1:155218991-155219081 | Common:1; Rare:23 | ||||
chr1:155227415-155227764 | Common:3; Rare:101 | ||||
chr1:155309934-155310158 | Common:1; Rare:62 | ||||
chr1:155313407-155313520 | Rare:17 | ||||
chr1:155338189-155338539 | Rare:81 | ||||
chr1:155343614-155343845 | Common:1; Rare:57 | ||||
chr1:155354516-155354822 | Rare:69 | ||||
chr1:155977104-155977240 | Rare:18 | ||||
chr1:155983360-155983747 | Rare:65 | ||||
chr1:156130309-156130773 | Common:3; Rare:113; Clinvar:11; Clinvar (benign):6; Clinvar (pathogenic):6 | ||||
chr1:156661418-156661517 | Rare:23 | ||||
chr1:156800161-156800529 | Common:1; Rare:71 |