Variant report

Variant	rs9485128
Chromosome Location	chr6:147140858-147140859
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11964579	1.00[CHB][hapmap];1.00[EUR][1000 genomes]
rs17076418	1.00[CHB][hapmap]
rs17076421	1.00[CHB][hapmap];0.90[ASN][1000 genomes]
rs2328768	1.00[CHB][hapmap]
rs56198525	0.90[ASN][1000 genomes]
rs6906745	0.90[ASN][1000 genomes]
rs6923489	1.00[ASN][1000 genomes]
rs6939002	1.00[ASN][1000 genomes]
rs73786784	1.00[ASN][1000 genomes]
rs7738936	1.00[ASN][1000 genomes]
rs7767826	1.00[EUR][1000 genomes]
rs7773366	1.00[ASN][1000 genomes]
rs9485126	1.00[EUR][1000 genomes]
rs9485127	1.00[EUR][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	nsv830838	chr6:147090745-147274669	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
2	nsv966634	chr6:147128760-147141217	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:147136000-147141200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr6:147137800-147141400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr6:147140400-147141600	Enhancers	Osteobl	bone
4	chr6:147140600-147141600	Enhancers	K562	blood
5	chr6:147140600-147141600	Enhancers	NH-A	brain
6	chr6:147140600-147141800	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr6:147140800-147141000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr6:147140800-147141200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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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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