Variant report

Variant	rs7092668
Chromosome Location	chr10:4091343-4091344
allele	C/T
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:5)

rs_ID	r²[population]
rs10508275	0.81[CHD][hapmap]
rs11252345	0.81[CHD][hapmap]
rs4147111	0.94[ASN][1000 genomes]
rs72774769	0.84[ASN][1000 genomes]
rs72774770	0.84[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	nsv1051297	chr10:3908706-4277678	Enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
2	nsv831772	chr10:4039292-4212218	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv1046213	chr10:4059937-4144692	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv540460	chr10:4059937-4144692	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:4087200-4092200	Weak transcription	Primary monocytes fromperipheralblood	blood
2	chr10:4087200-4092800	Weak transcription	Adipose Nuclei	Adipose
3	chr10:4087200-4093200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr10:4087400-4093000	Weak transcription	HUVEC	blood vessel
5	chr10:4087400-4093400	Weak transcription	Fetal Muscle Leg	muscle
6	chr10:4088800-4093200	Weak transcription	Primary B cells from peripheral blood	blood
7	chr10:4089400-4093200	Weak transcription	Fetal Kidney	kidney
8	chr10:4089600-4092800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr10:4091000-4091800	Weak transcription	Left Ventricle	heart
10	chr10:4091000-4092000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr10:4091000-4092000	Weak transcription	Ovary	ovary
12	chr10:4091000-4092800	Weak transcription	Small Intestine	intestine
13	chr10:4091000-4093000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr10:4091200-4093400	Weak transcription	Aorta	Aorta
15	chr10:4091200-4093400	Weak transcription	Colon Smooth Muscle	Colon
16	chr10:4091200-4093400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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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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