Variant report

Variant	rs7695495
Chromosome Location	chr4:152957898-152957899
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10003555	0.82[AMR][1000 genomes]
rs11099840	0.91[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12509941	0.84[AMR][1000 genomes]
rs13106080	1.00[ASN][1000 genomes]
rs13107216	1.00[CHB][hapmap]
rs13123917	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs13130547	1.00[ASN][1000 genomes]
rs13130730	1.00[ASN][1000 genomes]
rs13143024	0.91[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs13149643	0.96[AFR][1000 genomes];0.91[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1469241	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17276149	0.84[AMR][1000 genomes]
rs17276212	0.86[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4549360	0.82[AMR][1000 genomes]
rs4696123	0.84[AMR][1000 genomes]
rs7683987	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs890177	0.90[AFR][1000 genomes];0.87[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs919013	0.90[AFR][1000 genomes];0.88[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs9997649	0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv432644	chr4:152635395-153023402	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
2	nsv880341	chr4:152861685-153110256	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv931416	chr4:152877808-153440553	Genic enhancers Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
4	nsv461679	chr4:152935555-152992741	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv595734	chr4:152935555-152992741	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:152952000-152959000	Weak transcription	Aorta	Aorta
2	chr4:152954400-152958800	Weak transcription	HSMMtube	muscle
3	chr4:152954600-152958000	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr4:152954600-152959000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr4:152955000-152958000	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr4:152955000-152959000	Weak transcription	Right Atrium	heart
7	chr4:152955000-152959000	Weak transcription	Stomach Smooth Muscle	stomach
8	chr4:152955200-152960600	Weak transcription	Left Ventricle	heart
9	chr4:152957200-152958400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr4:152957200-152958800	Enhancers	Fetal Heart	heart
11	chr4:152957200-152960400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr4:152957400-152958200	Enhancers	NHLF	lung
13	chr4:152957600-152958000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
14	chr4:152957800-152958000	Enhancers	iPS-15b Cell Line	embryonic stem cell

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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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