Variant report

Variant	rs206741
Chromosome Location	chr6:164516081-164516082
allele	C/T
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]
rs12173338	0.84[MKK][hapmap]
rs169580	1.00[CEU][hapmap]
rs176242	0.85[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs206699	0.83[ASN][1000 genomes]
rs206700	0.95[CEU][hapmap]
rs206705	0.91[CEU][hapmap]
rs206707	0.90[CEU][hapmap]
rs206708	0.95[CEU][hapmap];0.81[CHB][hapmap]
rs206723	0.83[CEU][hapmap]
rs206726	0.83[CEU][hapmap]
rs206728	0.83[CEU][hapmap]
rs206739	0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[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	nsv1018860	chr6:163939347-164532579	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv538526	chr6:163939347-164532579	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
3	nsv1026707	chr6:164188210-164749206	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv538527	chr6:164188210-164749206	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
5	nsv1029952	chr6:164463355-165268911	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:164506400-164530200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr6:164507000-164519200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr6:164507800-164518000	Weak transcription	Right Ventricle	heart
4	chr6:164515000-164518000	Weak transcription	Left Ventricle	heart
5	chr6:164515000-164518600	Weak transcription	Psoas Muscle	Psoas
6	chr6:164515000-164519000	Weak transcription	HSMMtube	muscle
7	chr6:164515000-164522800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr6:164515200-164518400	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr6:164515800-164516200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr6:164515800-164516600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr6:164515800-164517400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr6:164516000-164516600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr6:164516000-164516600	Enhancers	NHDF-Ad	bronchial

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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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