Variant report

Variant	rs74069951
Chromosome Location	chr14:84912614-84912615
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs11847910	1.00[AMR][1000 genomes]
rs60695422	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74069957	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74069958	0.85[AFR][1000 genomes];1.00[AMR][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	esv2751288	chr14:84815330-85704047	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:84911000-84913200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr14:84912600-84912800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr14:84912600-84912800	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr14:84912600-84913000	Enhancers	iPS-18 Cell Line	embryonic stem cell

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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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