Variant report

Variant	rs61655667
Chromosome Location	chr2:151937504-151937505
allele	A/G
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:18)

rs_ID	r²[population]
rs10167013	0.89[EUR][1000 genomes]
rs10177678	0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10179177	0.89[EUR][1000 genomes]
rs10181655	0.89[EUR][1000 genomes]
rs10200462	0.89[EUR][1000 genomes]
rs12233051	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12233244	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1485096	0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs16829494	0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs16829500	0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs16829541	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs16829561	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2341849	0.82[ASN][1000 genomes]
rs4144513	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4144514	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57376641	0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs61116609	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6745933	0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv525350	chr2:151711700-152044794	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv523849	chr2:151718133-152143524	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
3	esv3693426	chr2:151725792-152295862	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
4	nsv1002140	chr2:151833257-152054910	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:151927400-151941000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr2:151937200-151937800	Enhancers	HUES6 Cell Line	embryonic stem cell
3	chr2:151937200-151938000	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr2:151937400-151938000	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr2:151937400-151938200	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr2:151937400-151938200	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr2:151937400-151938200	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr2:151937400-151938200	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr2:151937400-151941000	Weak transcription	H1 Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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