Variant report

Variant	rs74108014
Chromosome Location	chr1:103299083-103299084
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs553038	1.00[AFR][1000 genomes]
rs55937921	1.00[AFR][1000 genomes]
rs57389925	1.00[AFR][1000 genomes]
rs57437661	1.00[AFR][1000 genomes]
rs59896004	0.84[AFR][1000 genomes]
rs60602655	1.00[AFR][1000 genomes]
rs74108015	1.00[AFR][1000 genomes]
rs74108016	1.00[AFR][1000 genomes]
rs74108017	1.00[AFR][1000 genomes]
rs74108018	1.00[AFR][1000 genomes]
rs74108021	1.00[AFR][1000 genomes]
rs74108023	1.00[AFR][1000 genomes]
rs74108025	1.00[AFR][1000 genomes]
rs74108026	0.84[AFR][1000 genomes]
rs74108034	0.84[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830882	chr1:103192683-103355802	Weak transcription Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:103293000-103299200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr1:103299000-103299800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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