Variant report

Variant	rs12744632
Chromosome Location	chr1:170536797-170536798
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10753816	0.84[ASN][1000 genomes]
rs10919432	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11583564	0.84[CEU][hapmap];1.00[CHB][hapmap]
rs11801783	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12071298	0.92[AFR][1000 genomes];0.83[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs12075840	0.88[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs12729774	1.00[CHB][hapmap]
rs12731618	1.00[ASN][1000 genomes]
rs12743310	0.99[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12755330	0.91[CEU][hapmap];1.00[CHB][hapmap]
rs6663850	0.96[ASN][1000 genomes]
rs6676293	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs7515690	1.00[CHB][hapmap]
rs7552922	0.82[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs913257	1.00[JPT][hapmap]
rs9919189	0.84[ASN][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	nsv872543	chr1:170171083-170674903	Weak transcription Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
2	nsv533915	chr1:170258766-170725296	Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:170531400-170537600	Enhancers	NHDF-Ad	bronchial
2	chr1:170532800-170538600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr1:170533400-170536800	Weak transcription	Fetal Muscle Leg	muscle
4	chr1:170533800-170537400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr1:170534000-170537000	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr1:170535400-170537200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr1:170535600-170537200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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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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