Variant report

Variant	rs72732392
Chromosome Location	chr14:72316220-72316221
allele	C/T
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:13)

rs_ID	r²[population]
rs11158915	0.93[EUR][1000 genomes]
rs12896381	0.84[EUR][1000 genomes]
rs1892560	0.97[AFR][1000 genomes];0.80[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2533058	0.81[AFR][1000 genomes];0.99[EUR][1000 genomes]
rs2533059	0.88[EUR][1000 genomes]
rs72732389	0.97[AFR][1000 genomes];0.80[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72732390	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72732400	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72732401	0.97[AFR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72734003	0.97[AFR][1000 genomes];0.80[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72734014	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8018260	0.89[EUR][1000 genomes]
rs8019244	0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3398985	chr14:71927884-72404676	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv530794	chr14:72113818-73034008	Enhancers Bivalent/Poised TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:72315600-72316600	Active TSS	H9 Cell Line	embryonic stem cell
2	chr14:72315800-72316400	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr14:72316000-72316400	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr14:72316000-72316600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
5	chr14:72316000-72319000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr14:72316200-72316400	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
7	chr14:72316200-72316600	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr14:72316200-72316600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr14:72316200-72317000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr14:72316200-72317200	ZNF genes & repeats	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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