Variant report

Variant	rs11591252
Chromosome Location	chr10:16285822-16285823
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10508504	0.93[EUR][1000 genomes]
rs10904697	0.97[EUR][1000 genomes]
rs10904699	0.97[EUR][1000 genomes]
rs11253863	0.97[EUR][1000 genomes]
rs11253865	1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12247591	0.90[EUR][1000 genomes]
rs7082336	0.94[EUR][1000 genomes]
rs7094549	0.90[EUR][1000 genomes]
rs7095122	0.92[EUR][1000 genomes]
rs74124947	0.82[EUR][1000 genomes]
rs74124951	0.84[EUR][1000 genomes]
rs7902512	0.94[EUR][1000 genomes]
rs7910600	0.82[EUR][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	nsv530146	chr10:15722937-16522747	Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
2	nsv870420	chr10:16225427-16541252	Flanking Active TSS Strong transcription Enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv894904	chr10:16233175-16477106	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv831796	chr10:16240111-16393044	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	esv19845	chr10:16284959-16291617	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:16284200-16286600	Enhancers	H1 Cell Line	embryonic stem cell
2	chr10:16284400-16286200	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr10:16284800-16286000	Enhancers	H9 Cell Line	embryonic stem cell
4	chr10:16285000-16286000	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr10:16285000-16286200	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr10:16285200-16286000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
7	chr10:16285400-16286000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr10:16285400-16286000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr10:16285600-16286800	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr10:16285800-16286000	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr10:16285800-16286200	Enhancers	HUES48 Cell Line	embryonic stem cell

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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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