Variant report

Variant	rs7763686
Chromosome Location	chr6:4824198-4824199
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs1265336	0.88[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap]
rs1771884	0.87[ASN][1000 genomes]
rs1883327	0.89[CHB][hapmap];0.92[CHD][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs233477	0.88[CHB][hapmap];0.91[CHD][hapmap];1.00[JPT][hapmap]
rs233479	0.94[CHB][hapmap];0.96[CHD][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs55653939	0.91[ASN][1000 genomes]
rs6925763	0.84[ASN][1000 genomes]
rs73364556	0.82[ASN][1000 genomes]
rs7772813	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs808603	0.81[ASN][1000 genomes]
rs808615	0.82[CHB][hapmap];0.83[CHD][hapmap];1.00[JPT][hapmap]
rs808622	0.82[CHB][hapmap];1.00[JPT][hapmap]

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	esv3366530	chr6:4471528-4865322	ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv1023527	chr6:4729592-5387176	Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	esv2422499	chr6:4745428-5073222	Enhancers Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
4	nsv1015888	chr6:4787784-4883663	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv966675	chr6:4819733-4855009	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:4806800-4829400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr6:4807200-4827800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr6:4812400-4829600	Weak transcription	Left Ventricle	heart
4	chr6:4812600-4826800	Weak transcription	HepG2	liver
5	chr6:4812800-4828800	Weak transcription	Hela-S3	cervix
6	chr6:4814200-4829600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr6:4815000-4826000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr6:4815000-4827400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr6:4815200-4824200	Weak transcription	Primary B cells from cord blood	blood
10	chr6:4815200-4829600	Weak transcription	Lung	lung
11	chr6:4817800-4827000	Weak transcription	K562	blood
12	chr6:4820200-4828000	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr6:4820400-4825400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
14	chr6:4820400-4844200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr6:4820800-4825400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr6:4821200-4853600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr6:4823600-4824200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
18	chr6:4824000-4824200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood

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dbSNP/dbVar ID: rs12345 /nsv7879
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