Variant report

Variant	rs60102359
Chromosome Location	chr6:70848394-70848395
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs1200561	0.81[AFR][1000 genomes]
rs56855480	0.85[AMR][1000 genomes]
rs810561	0.87[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1026151	chr6:70621616-70946967	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv933674	chr6:70663616-70973112	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv1026836	chr6:70727747-70849014	Enhancers Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv932111	chr6:70736835-71633094	Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
5	nsv886142	chr6:70741209-71251421	Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
6	nsv830683	chr6:70743422-70941190	Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:70842400-70875200	Weak transcription	GM12878-XiMat	blood
2	chr6:70845400-70849000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr6:70845600-70849000	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr6:70845600-70851600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr6:70846400-70848800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr6:70846400-70848800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr6:70846400-70849200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr6:70846600-70849200	Strong transcription	Primary B cells from cord blood	blood
9	chr6:70846800-70850600	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr6:70847600-70849400	Enhancers	H9 Cell Line	embryonic stem cell
11	chr6:70847600-70874800	Strong transcription	Primary B cells from peripheral blood	blood
12	chr6:70847800-70849000	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr6:70848000-70848400	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr6:70848000-70849800	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr6:70848200-70848600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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