Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:100249810-100249989 | Common:2; Rare:58; Clinvar:1; Clinvar (benign):1 | ||||
chr1:100266093-100266344 | Common:6; Rare:152 | ||||
chr1:100352130-100352570 | Common:1; Rare:153 | ||||
chr1:100894630-100895052 | Common:4; Rare:166 | ||||
chr1:100895080-100895370 | Common:4; Rare:72 | ||||
chr1:100895861-100896257 | Rare:187 | ||||
chr1:101025732-101025947 | Common:2; Rare:115 | ||||
chr1:101026100-101026364 | Rare:69 | ||||
chr1:103525461-103525766 | Rare:147 | ||||
chr1:103525869-103526074 | Common:1; Rare:92 | ||||
chr1:107056598-107056723 | Common:2; Rare:91 | ||||
chr1:107688406-107688669 | Rare:73 | ||||
chr1:108200076-108200494 | Common:18; Rare:251 | ||||
chr1:108559851-108560323 | Common:6; Rare:295 | ||||
chr1:108660670-108660960 | Common:8; Rare:146 |