Variant report

Variant	rs56379016
Chromosome Location	chr11:92651684-92651685
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs1052382	0.95[EUR][1000 genomes]
rs11598	0.95[EUR][1000 genomes]
rs17628334	0.97[EUR][1000 genomes]
rs1838977	0.90[AFR][1000 genomes];0.97[EUR][1000 genomes]
rs2028979	0.90[AFR][1000 genomes];0.97[EUR][1000 genomes]
rs55835347	0.97[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7950811	0.90[AFR][1000 genomes];0.97[EUR][1000 genomes]
rs7950849	0.90[AFR][1000 genomes];0.97[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1043861	chr11:92357570-92689868	Strong transcription Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
2	nsv1044571	chr11:92495213-92742314	Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
3	nsv898175	chr11:92623349-92668826	Genic enhancers Weak transcription Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
4	nsv555903	chr11:92640787-92877533	Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv555904	chr11:92640787-92881933	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 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	chr11:92649800-92653000	Enhancers	ES-I3 Cell Line	embryonic stem cell
2	chr11:92650400-92652600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
3	chr11:92650600-92652400	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr11:92650600-92652800	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr11:92650600-92653200	Enhancers	H9 Cell Line	embryonic stem cell
6	chr11:92651000-92652400	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr11:92651200-92653000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr11:92651400-92651800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr11:92651400-92651800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
10	chr11:92651400-92651800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
11	chr11:92651400-92653400	Weak transcription	Cortex derived primary cultured neurospheres	brain
12	chr11:92651400-92655400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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