Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:58783078-58783140 | Common:1; Rare:16 | ||||
chr1:58783151-58783340 | Rare:47 | ||||
chr1:58783352-58783681 | Common:1; Rare:76 | ||||
chr1:65066721-65066942 | Rare:73 | ||||
chr1:65067712-65067825 | Rare:30 | ||||
chr1:67832100-67832224 | Common:1; Rare:33 | ||||
chr1:83860974-83861127 | Rare:36 | ||||
chr1:90851568-90851812 | Common:2; Rare:62 | ||||
chr1:92837208-92837592 | Common:1; Rare:99; Clinvar (benign):1 | ||||
chr1:103573958-103574418 | Common:1; Rare:159 | ||||
chr1:103623332-103623494 | Common:3; Rare:12 | ||||
chr1:109100441-109100461 | Rare:5 | ||||
chr1:112360596-112360920 | Rare:67 | ||||
chr1:120558520-120558651 | Rare:33 | ||||
chr1:144551931-144552215 | Rare:92 |