Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:39408710-39409102 | Common:10; Rare:274 | ||||
chr1:39575420-39576551 | Common:8; Rare:479 | ||||
chr1:39576527-39576981 | Rare:210 | ||||
chr1:39738717-39738911 | Common:3; Rare:63 | ||||
chr1:39788826-39789155 | Common:7; Rare:191 | ||||
chr1:39883441-39883602 | Common:2; Rare:122; Clinvar (pathogenic):2 | ||||
chr1:39902002-39902219 | Common:2; Rare:59 | ||||
chr1:40039875-40040073 | Common:3; Rare:90 | ||||
chr1:40040409-40040864 | Common:8; Rare:279 | ||||
chr1:40161225-40161416 | Common:2; Rare:97 | ||||
chr1:40257898-40258296 | Common:8; Rare:212; Clinvar:15; Clinvar (benign):2 | ||||
chr1:40449780-40450360 | Common:10; Rare:245 | ||||
chr1:40508649-40508815 | Common:7; Rare:76 | ||||
chr1:40531360-40531770 | Common:3; Rare:173 | ||||
chr1:40691323-40692021 | Common:5; Rare:380 |