Variant report

Variant	rs72823152
Chromosome Location	chr2:77214845-77214846
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs1348832	0.97[ASN][1000 genomes]
rs1348833	0.97[ASN][1000 genomes]
rs1446716	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs17013541	1.00[ASN][1000 genomes]
rs2028914	1.00[ASN][1000 genomes]
rs58463979	0.86[AFR][1000 genomes]
rs59946045	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs61145558	0.86[AFR][1000 genomes]
rs61391187	0.81[ASN][1000 genomes]
rs72821297	0.86[AFR][1000 genomes]
rs72821299	0.86[AFR][1000 genomes]
rs72823111	0.86[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs72823116	0.86[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs72823136	0.90[ASN][1000 genomes]
rs72823138	0.86[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs72823139	0.86[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs72823141	0.86[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs72823142	1.00[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs72823144	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs72823157	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs72823158	1.00[ASN][1000 genomes]
rs72823159	1.00[ASN][1000 genomes]
rs72823168	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs72823173	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs72823179	0.93[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	esv2752990	chr2:77038541-77217310	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv834266	chr2:77120236-77287504	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv949670	chr2:77125218-77712607	Weak transcription Enhancers Bivalent Enhancer Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv519950	chr2:77213103-77256291	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:77213600-77215400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr2:77214000-77220400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr2:77214200-77217400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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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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