Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:10108311-10108717 | Rare:172 | ||||
chr1:10168980-10169290 | Common:2; Rare:41 | ||||
chr1:10173720-10174000 | Common:3; Rare:69 | ||||
chr1:10283473-10283581 | Rare:18 | ||||
chr1:10378451-10378851 | Common:3; Rare:81; Clinvar:6; Clinvar (benign):7 | ||||
chr1:10388080-10388430 | Common:1; Rare:70 | ||||
chr1:10416999-10417955 | Common:2; Rare:273 | ||||
chr1:10494769-10494910 | Rare:30 | ||||
chr1:10495141-10495588 | Common:1; Rare:247; Clinvar:5 | ||||
chr1:10510865-10511679 | Common:5; Rare:239 | ||||
chr1:10511643-10512043 | Common:4; Rare:111 | ||||
chr1:10516250-10516570 | Rare:52 | ||||
chr1:10555760-10556030 | Common:1; Rare:56 | ||||
chr1:10556360-10556660 | Common:4; Rare:102 | ||||
chr1:10594692-10594960 | Common:4; Rare:70 |