Variant report

Variant	rs73390178
Chromosome Location	chr6:27390489-27390490
allele	A/G
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:13)

rs_ID	r²[population]
rs11961344	1.00[AMR][1000 genomes]
rs16867879	1.00[ASN][1000 genomes]
rs16897468	1.00[ASN][1000 genomes]
rs16897553	1.00[ASN][1000 genomes]
rs16901818	1.00[ASN][1000 genomes]
rs56809760	1.00[ASN][1000 genomes]
rs57759431	1.00[ASN][1000 genomes]
rs73389539	1.00[AMR][1000 genomes]
rs73389547	1.00[AMR][1000 genomes]
rs73391371	1.00[ASN][1000 genomes]
rs73392621	1.00[ASN][1000 genomes]
rs73392632	1.00[AMR][1000 genomes]
rs73395363	1.00[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	nsv948921	chr6:26556890-27443957	Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	472 gene(s)	inside rSNPs	diseases
2	nsv1031803	chr6:27355881-27423655	Active TSS Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
3	nsv538166	chr6:27355881-27423655	Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
4	nsv5235	chr6:27358498-27404074	ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:27390400-27390600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr6:27390400-27390800	Active TSS	Fetal Muscle Leg	muscle
3	chr6:27390400-27391000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr6:27390400-27391000	Active TSS	Ovary	ovary
5	chr6:27390400-27391200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr6:27390400-27391200	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr6:27390400-27391200	Active TSS	Brain Inferior Temporal Lobe	brain

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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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