Variant report

Variant	rs6844961
Chromosome Location	chr4:76785187-76785188
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10856862	1.00[EUR][1000 genomes]
rs13149236	1.00[EUR][1000 genomes]
rs1546567	1.00[EUR][1000 genomes]
rs1546568	1.00[EUR][1000 genomes]
rs17000735	1.00[EUR][1000 genomes]
rs17000764	1.00[EUR][1000 genomes]
rs17000810	1.00[EUR][1000 genomes]
rs17000961	1.00[EUR][1000 genomes]
rs17000973	1.00[EUR][1000 genomes]
rs17001036	1.00[EUR][1000 genomes]
rs17001150	1.00[EUR][1000 genomes]
rs17001165	1.00[EUR][1000 genomes]
rs2174513	1.00[EUR][1000 genomes]
rs28406977	1.00[EUR][1000 genomes]
rs34155925	1.00[EUR][1000 genomes]
rs4324568	1.00[EUR][1000 genomes]
rs4859563	1.00[EUR][1000 genomes]
rs5028031	1.00[EUR][1000 genomes]
rs56024633	1.00[EUR][1000 genomes]
rs57659593	1.00[EUR][1000 genomes]
rs61288563	1.00[EUR][1000 genomes]
rs6531992	1.00[EUR][1000 genomes]
rs6811934	1.00[EUR][1000 genomes]
rs6824610	1.00[EUR][1000 genomes]
rs6826893	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6838414	1.00[EUR][1000 genomes]
rs6856987	1.00[EUR][1000 genomes]
rs73825563	1.00[EUR][1000 genomes]
rs73825569	1.00[EUR][1000 genomes]
rs73825570	1.00[EUR][1000 genomes]
rs7654738	1.00[EUR][1000 genomes]
rs7685485	1.00[EUR][1000 genomes]
rs7685710	1.00[EUR][1000 genomes]
rs7693116	1.00[EUR][1000 genomes]
rs9998204	1.00[EUR][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	esv3353539	chr4:76530136-76993859	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
2	nsv529613	chr4:76654941-77081576	Flanking Active TSS Weak transcription Genic enhancers Strong transcription Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:76782600-76789600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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Input of quick search could be:

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

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