Variant report

Variant	rs7664735
Chromosome Location	chr4:69141613-69141614
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10024896	1.00[EUR][1000 genomes]
rs10027564	1.00[EUR][1000 genomes]
rs10031034	1.00[EUR][1000 genomes]
rs11932381	1.00[EUR][1000 genomes]
rs11940780	1.00[EUR][1000 genomes]
rs11942378	1.00[EUR][1000 genomes]
rs17089253	1.00[EUR][1000 genomes]
rs2056802	1.00[EUR][1000 genomes]
rs28633232	1.00[EUR][1000 genomes]
rs28758556	1.00[EUR][1000 genomes]
rs28866177	1.00[EUR][1000 genomes]
rs35883654	1.00[EUR][1000 genomes]
rs7684922	1.00[EUR][1000 genomes]
rs9998289	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1008084	chr4:68797598-69482831	Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
2	nsv537131	chr4:68797598-69482831	Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
3	esv1812438	chr4:68943858-69154222	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
4	esv1806586	chr4:68943858-69592846	ZNF genes & repeats Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
5	nsv461546	chr4:69049643-69223057	Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
6	nsv594506	chr4:69049643-69223057	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
7	nsv964740	chr4:69137797-69159003	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr4:69138800-69143600	Weak transcription	Muscle Satellite Cultured Cells	--
2	chr4:69139400-69143400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr4:69139400-69143600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr4:69139400-69149600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr4:69139600-69147400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr4:69139600-69153600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr4:69139800-69143600	Weak transcription	Osteobl	bone
8	chr4:69140000-69143600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr4:69140200-69143600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
10	chr4:69140400-69143400	Weak transcription	H1 Cell Line	embryonic stem cell
11	chr4:69140400-69145800	Weak transcription	Fetal Intestine Small	intestine
12	chr4:69140400-69146000	Weak transcription	Fetal Intestine Large	intestine
13	chr4:69140600-69142200	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr4:69140800-69143200	Weak transcription	HUES48 Cell Line	embryonic stem cell
15	chr4:69140800-69143800	Weak transcription	HUES64 Cell Line	embryonic stem cell

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

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