Variant report

Variant	rs919856
Chromosome Location	chr4:21083553-21083554
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 63 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs10007120	0.81[ASN][1000 genomes]
rs10028465	0.96[ASN][1000 genomes]
rs10028561	0.97[ASN][1000 genomes]
rs10029228	0.81[ASN][1000 genomes]
rs10033946	0.89[YRI][hapmap]
rs1023722	0.85[CHB][hapmap];0.95[CHD][hapmap];0.85[JPT][hapmap]
rs10938829	0.85[CHB][hapmap];0.85[JPT][hapmap]
rs11944192	0.85[CHB][hapmap];0.81[ASN][1000 genomes]
rs12642991	0.84[ASN][1000 genomes]
rs12643360	0.84[CEU][hapmap];0.84[CHB][hapmap]
rs12643371	0.81[ASN][1000 genomes]
rs12646516	0.81[ASN][1000 genomes]
rs12649352	0.81[ASN][1000 genomes]
rs12649359	0.82[ASN][1000 genomes]
rs1368640	0.83[CEU][hapmap];1.00[CHB][hapmap]
rs1433493	0.81[ASN][1000 genomes]
rs1560786	0.81[ASN][1000 genomes]
rs1560788	0.85[CHB][hapmap];0.81[ASN][1000 genomes]
rs1560789	0.82[CEU][hapmap];0.85[CHB][hapmap]
rs1560790	0.81[ASN][1000 genomes]
rs16870359	0.85[CHB][hapmap]
rs16870421	0.85[CHB][hapmap];0.84[ASN][1000 genomes]
rs1865193	0.92[CHB][hapmap];0.85[JPT][hapmap]
rs1897664	0.84[CEU][hapmap];0.85[CHB][hapmap];0.81[ASN][1000 genomes]
rs28390301	0.81[ASN][1000 genomes]
rs28396704	1.00[ASN][1000 genomes]
rs28492736	0.81[ASN][1000 genomes]
rs28718441	1.00[ASN][1000 genomes]
rs61277470	0.84[ASN][1000 genomes]
rs6448011	0.92[CHB][hapmap];0.95[CHD][hapmap];0.80[GIH][hapmap];0.85[JPT][hapmap];1.00[ASN][1000 genomes]
rs6448013	0.86[CEU][hapmap];0.92[CHB][hapmap];0.85[JPT][hapmap];1.00[ASN][1000 genomes]
rs6448016	0.84[CEU][hapmap];0.85[CHB][hapmap];0.81[ASN][1000 genomes]
rs6448018	0.81[ASN][1000 genomes]
rs6448019	0.84[ASN][1000 genomes]
rs6814358	0.84[CEU][hapmap];0.85[CHB][hapmap];0.81[ASN][1000 genomes]
rs6824763	0.89[CEU][hapmap];0.92[CHB][hapmap];0.85[JPT][hapmap];1.00[ASN][1000 genomes]
rs7356370	0.84[CEU][hapmap];0.85[CHB][hapmap];0.81[ASN][1000 genomes]
rs7356371	0.81[ASN][1000 genomes]
rs7667541	0.84[CEU][hapmap];0.85[CHB][hapmap];0.81[ASN][1000 genomes]
rs7673495	0.85[CHB][hapmap];0.84[JPT][hapmap];0.84[ASN][1000 genomes]
rs7688396	0.81[ASN][1000 genomes]
rs7689134	0.81[ASN][1000 genomes]
rs7689193	0.84[CEU][hapmap];0.85[CHB][hapmap];0.81[ASN][1000 genomes]
rs7689340	0.84[CEU][hapmap];0.84[CHB][hapmap];0.81[ASN][1000 genomes]
rs7694857	0.81[ASN][1000 genomes]
rs7695039	0.81[ASN][1000 genomes]
rs7695878	0.92[CHB][hapmap];0.95[CHD][hapmap];0.81[GIH][hapmap];0.85[JPT][hapmap];0.80[TSI][hapmap]
rs7696284	0.85[CHB][hapmap]
rs7696531	0.84[CEU][hapmap];0.91[CHB][hapmap]
rs7696822	0.81[CEU][hapmap];0.91[CHB][hapmap]
rs7696887	0.84[CEU][hapmap];0.85[CHB][hapmap];0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1014941	chr4:20611726-21345226	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv537053	chr4:20611726-21345226	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv1013365	chr4:20834054-21609078	Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
4	nsv829878	chr4:20966047-21138626	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv878745	chr4:21054348-21155716	Enhancers Weak transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv878746	chr4:21054348-21169062	Enhancers Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv878747	chr4:21057794-21169062	Enhancers Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
8	esv3467025	chr4:21080942-21086055	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
9	esv3467026	chr4:21080942-21086055	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
10	esv17854	chr4:21081080-21086557	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
11	esv2760912	chr4:21082551-21085342	Enhancers	n/a	n/a	inside rSNPs	diseases
12	nsv522328	chr4:21083553-21096827	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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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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