Variant report

Variant	rs4491863
Chromosome Location	chr3:70524412-70524413
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs11128176	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12490416	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13096169	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1491609	0.90[ASN][1000 genomes]
rs17790790	0.88[ASN][1000 genomes]
rs2320777	0.89[EUR][1000 genomes]
rs4572735	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4638930	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6549341	0.83[ASN][1000 genomes]
rs6796357	0.83[ASN][1000 genomes]
rs7431027	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7650600	0.87[ASN][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	nsv533396	chr3:69964029-70538306	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv3867	chr3:70480358-70525397	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	esv2762336	chr3:70516421-70527712	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	inside rSNPs	n/a

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:70521200-70524600	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr3:70524200-70524800	Enhancers	H9 Cell Line	embryonic stem cell
3	chr3:70524200-70525000	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr3:70524200-70525600	Enhancers	H1 Cell Line	embryonic stem cell
5	chr3:70524200-70526400	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr3:70524400-70524800	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr3:70524400-70525600	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr3:70524400-70526400	Enhancers	iPS-15b 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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