Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:93180053-93180751 | Common:2; Rare:272 | ||||
chr1:93345619-93345962 | Common:5; Rare:115 | ||||
chr1:93448019-93448170 | Common:1; Rare:57 | ||||
chr1:93847215-93847286 | Common:1; Rare:17 | ||||
chr1:93879088-93879336 | Common:3; Rare:97 | ||||
chr1:94237492-94237744 | Rare:93 | ||||
chr1:94541622-94542000 | Common:1; Rare:110 | ||||
chr1:94820186-94820403 | Common:3; Rare:57 | ||||
chr1:94903176-94903444 | Common:1; Rare:52 | ||||
chr1:94926854-94926933 | Rare:22 | ||||
chr1:94926940-94927467 | Common:4; Rare:167 | ||||
chr1:95072855-95073023 | Common:1; Rare:67; Clinvar (benign):2 | ||||
chr1:95233945-95234237 | Common:5; Rare:86 | ||||
chr1:96721690-96721861 | Common:1; Rare:74 | ||||
chr1:98661609-98661869 | Common:2; Rare:93 |