Variant report

Variant	rs6864302
Chromosome Location	chr5:113793286-113793287
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs11949478	1.00[CEU][hapmap];1.00[AMR][1000 genomes]
rs17136613	1.00[AMR][1000 genomes]
rs17136662	1.00[CEU][hapmap];0.82[LWK][hapmap];0.81[MKK][hapmap];0.90[YRI][hapmap];1.00[AMR][1000 genomes]
rs17136705	1.00[AMR][1000 genomes]
rs55942406	1.00[AMR][1000 genomes]
rs56284400	1.00[AMR][1000 genomes]
rs56789529	1.00[AMR][1000 genomes]
rs56976419	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57220263	1.00[AMR][1000 genomes]
rs57876273	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58946775	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61514079	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61530176	1.00[AMR][1000 genomes]
rs6897063	1.00[CEU][hapmap];0.82[LWK][hapmap];1.00[AMR][1000 genomes]
rs73247838	1.00[AMR][1000 genomes]
rs73247848	1.00[AMR][1000 genomes]
rs73247849	1.00[AMR][1000 genomes]
rs73779903	1.00[AMR][1000 genomes]
rs972756	1.00[AMR][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	nsv830451	chr5:113684301-113829833	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv882729	chr5:113743628-114497708	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:113786600-113793400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr5:113791800-113793600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr5:113792800-113794200	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr5:113793000-113793400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr5:113793000-113794800	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr5:113793000-113794800	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr5:113793200-113793600	Enhancers	H1 Cell Line	embryonic stem cell
8	chr5:113793200-113793600	Enhancers	H9 Cell Line	embryonic stem cell
9	chr5:113793200-113793600	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr5:113793200-113793800	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr5:113793200-113793800	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr5:113793200-113794200	Enhancers	ES-I3 Cell Line	embryonic stem cell

Quick Search:

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

what's new

Quick links