Variant report

Variant	rs74064279
Chromosome Location	chr14:81042617-81042618
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs57127927	1.00[AMR][1000 genomes]
rs57644214	1.00[AMR][1000 genomes]
rs58599638	1.00[AMR][1000 genomes]
rs58687069	1.00[AMR][1000 genomes]
rs58804464	1.00[AMR][1000 genomes]
rs59450199	1.00[AMR][1000 genomes]
rs59619003	1.00[AMR][1000 genomes]
rs60698271	1.00[AMR][1000 genomes]
rs60764374	1.00[AMR][1000 genomes]
rs61216637	1.00[AMR][1000 genomes]
rs61336262	1.00[AMR][1000 genomes]
rs61345181	1.00[AMR][1000 genomes]
rs61419086	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869348	chr14:80921098-81535754	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv902116	chr14:81018237-81082400	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:81029600-81044800	Weak transcription	Dnd41	blood
2	chr14:81037000-81051000	Weak transcription	NHEK	skin
3	chr14:81037200-81050800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr14:81037200-81050800	Weak transcription	HMEC	breast
5	chr14:81041400-81042800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr14:81041400-81046200	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr14:81042000-81043000	Enhancers	A549	lung
8	chr14:81042400-81042800	Enhancers	Pancreatic Islets	Pancreatic Islet
9	chr14:81042400-81043200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr14:81042600-81042800	Enhancers	iPS-20b 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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