Variant report

Variant	rs73691210
Chromosome Location	chr8:66794747-66794748
allele	G/T
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]
rs16932400	1.00[EUR][1000 genomes]
rs2357573	1.00[EUR][1000 genomes]
rs55658547	1.00[EUR][1000 genomes]
rs55947988	1.00[EUR][1000 genomes]
rs56158968	1.00[EUR][1000 genomes]
rs56316549	1.00[EUR][1000 genomes]
rs56338345	1.00[EUR][1000 genomes]
rs56781848	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57028955	1.00[EUR][1000 genomes]
rs57400902	1.00[EUR][1000 genomes]
rs57598287	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58772235	1.00[EUR][1000 genomes]
rs58852265	1.00[EUR][1000 genomes]
rs58975338	1.00[EUR][1000 genomes]
rs59084420	1.00[EUR][1000 genomes]
rs59461929	1.00[EUR][1000 genomes]
rs59658032	1.00[EUR][1000 genomes]
rs59865117	1.00[EUR][1000 genomes]
rs59967440	1.00[EUR][1000 genomes]
rs60088935	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60229346	1.00[EUR][1000 genomes]
rs60706814	1.00[EUR][1000 genomes]
rs61571778	1.00[EUR][1000 genomes]
rs6472243	1.00[EUR][1000 genomes]
rs7001194	1.00[EUR][1000 genomes]
rs73691221	1.00[EUR][1000 genomes]
rs73691248	1.00[EUR][1000 genomes]
rs73691253	1.00[EUR][1000 genomes]
rs73691255	1.00[EUR][1000 genomes]
rs73691258	1.00[EUR][1000 genomes]
rs73691260	1.00[EUR][1000 genomes]
rs73693441	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7814366	1.00[EUR][1000 genomes]
rs7834695	1.00[EUR][1000 genomes]
rs7839572	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	esv3446467	chr8:66749863-67667068	Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
2	nsv1023239	chr8:66775321-66904124	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	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	chr8:66787600-66795800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr8:66792400-66801000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
3	chr8:66794200-66799000	Weak transcription	Primary B cells from peripheral blood	blood
4	chr8:66794600-66794800	Flanking Active TSS	K562	blood

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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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