Variant report

Variant	rs7668162
Chromosome Location	chr4:171941803-171941804
allele	C/T
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:19)

rs_ID	r²[population]
rs12645591	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12715920	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1508509	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1588229	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1605652	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1605653	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1605654	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1818341	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1818342	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2877578	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2915629	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6843064	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs71646860	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72991717	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72991718	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72991720	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7340865	0.96[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs7663742	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs906624	0.97[AFR][1000 genomes];1.00[AMR][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	nsv881345	chr4:171673765-172228547	Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases
2	nsv1018793	chr4:171808272-172395180	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
3	nsv881662	chr4:171842726-171957000	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:171929000-171944400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr4:171939000-171944000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr4:171941600-171942200	Enhancers	H9 Cell Line	embryonic stem cell
4	chr4:171941800-171942200	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr4:171941800-171942800	Enhancers	HUES64 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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