Variant report

Variant	rs1155357
Chromosome Location	chr4:125421613-125421614
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10857101	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1492748	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1492752	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17008322	0.83[AMR][1000 genomes]
rs1873772	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs219848	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28592204	0.83[AMR][1000 genomes]
rs28668989	0.83[AMR][1000 genomes]
rs28730460	0.83[AMR][1000 genomes]
rs312507	0.85[AFR][1000 genomes]
rs312513	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs312515	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs312516	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs312519	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73845363	0.83[AMR][1000 genomes]
rs9992551	1.00[AFR][1000 genomes];1.00[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	nsv868977	chr4:124841128-125550637	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	nsv879880	chr4:125174817-125494547	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	esv2760890	chr4:125273456-125466931	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv879881	chr4:125280852-125448288	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr4:125420000-125423200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr4:125420400-125423000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr4:125420800-125422200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr4:125421400-125426200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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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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