Variant report

Variant	rs187811
Chromosome Location	chr6:142938768-142938769
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs11155255	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs12214216	1.00[CEU][hapmap]
rs146250	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs17527704	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs2202900	0.82[CEU][hapmap]
rs263106	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs263117	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs263128	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs263136	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs263153	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs263170	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs263173	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs865141	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs9390000	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949088	chr6:142561402-143128849	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv1023426	chr6:142813845-142940262	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv830827	chr6:142840734-143015005	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:142933600-142944000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr6:142937600-142939200	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr6:142937800-142938800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr6:142937800-142938800	Enhancers	NHEK	skin
5	chr6:142938000-142938800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr6:142938000-142938800	Enhancers	HMEC	breast

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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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