Variant report

Variant	rs73798027
Chromosome Location	chr5:151542176-151542177
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs56023602	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58015776	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58393037	1.00[AMR][1000 genomes]
rs60253952	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60883836	0.84[AFR][1000 genomes]
rs6881089	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6883512	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73795748	0.88[AFR][1000 genomes]
rs73796393	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73798033	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73798043	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73798050	0.84[AFR][1000 genomes]
rs73798056	1.00[AMR][1000 genomes]
rs73798057	1.00[AMR][1000 genomes]
rs73798922	1.00[AMR][1000 genomes]
rs7708592	1.00[AMR][1000 genomes]
rs7718285	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9918224	0.84[AFR][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	esv2760935	chr5:151463117-151586051	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv883040	chr5:151471642-151596273	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv516251	chr5:151514956-151543128	Enhancers Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv1023828	chr5:151522149-151956217	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 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	chr5:151542000-151542400	Enhancers	iPS-15b Cell Line	embryonic stem cell

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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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