Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:161314265-161314396 | Common:3; Rare:46; Clinvar (benign):2 | ||||
chr1:161766225-161766363 | Common:3; Rare:44 | ||||
chr1:162790516-162790797 | Common:4; Rare:84 | ||||
chr1:163321713-163322007 | Common:1; Rare:79 | ||||
chr1:165630780-165630874 | Rare:34 | ||||
chr1:165768796-165768933 | Common:1; Rare:64 | ||||
chr1:165827740-165827829 | Common:1; Rare:26 | ||||
chr1:166839286-166839530 | Rare:75 | ||||
chr1:166876229-166876528 | Common:1; Rare:96 | ||||
chr1:167935988-167936261 | Common:1; Rare:85 | ||||
chr1:167936561-167936924 | Common:1; Rare:131 | ||||
chr1:168178739-168179089 | Common:4; Rare:112 | ||||
chr1:168225891-168226050 | Common:1; Rare:57 | ||||
chr1:169367739-169368250 | Common:3; Rare:107 | ||||
chr1:169427388-169427574 | Rare:39 |