Variant report

Variant	rs56942091
Chromosome Location	chr7:70629438-70629439
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs56795865	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73357805	1.00[AMR][1000 genomes]
rs73361706	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73361714	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73361715	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73361726	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73361747	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73361771	1.00[AMR][1000 genomes]
rs73361776	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv519090	chr7:70085934-71071896	Weak transcription Enhancers Bivalent/Poised TSS Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1034662	chr7:70275712-70722953	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv1015261	chr7:70404302-71255933	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:70612000-70636400	Weak transcription	Ovary	ovary
2	chr7:70612200-70650600	Weak transcription	Fetal Lung	lung
3	chr7:70615200-70632800	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr7:70616000-70632800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr7:70617600-70630600	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr7:70619800-70641800	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr7:70620200-70631000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr7:70620400-70639000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr7:70623000-70630200	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr7:70623000-70633000	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr7:70623000-70639600	Weak transcription	Aorta	Aorta
12	chr7:70624800-70630800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
13	chr7:70626400-70630000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr7:70628000-70630400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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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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