Variant report

Variant	rs61423916
Chromosome Location	chr4:143831886-143831887
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs2012164	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28431183	1.00[AMR][1000 genomes]
rs28524896	1.00[AMR][1000 genomes]
rs56676496	1.00[AMR][1000 genomes]
rs57197698	1.00[AMR][1000 genomes]
rs58224636	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58494822	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs58597536	0.83[AMR][1000 genomes]
rs59762983	0.85[AFR][1000 genomes]
rs7679596	0.85[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv880174	chr4:143639498-143848024	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv880175	chr4:143779613-143892252	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv10580	chr4:143794158-143856359	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv830102	chr4:143820268-143953611	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	5 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	chr4:143830000-143832800	Weak transcription	Aorta	Aorta
2	chr4:143831200-143832000	Enhancers	Rectal Smooth Muscle	rectum
3	chr4:143831600-143834600	Weak transcription	Colon Smooth Muscle	Colon
4	chr4:143831600-143834800	Weak transcription	Stomach Smooth Muscle	stomach

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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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