Variant report

Variant	rs62519706
Chromosome Location	chr8:64992981-64992982
allele	G/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:11)

rs_ID	r²[population]
rs10504370	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12542208	0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs16930842	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs16930892	0.88[EUR][1000 genomes]
rs16930897	0.88[EUR][1000 genomes]
rs1838419	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs56254916	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs57006495	0.88[EUR][1000 genomes]
rs62510964	0.85[EUR][1000 genomes]
rs62519745	0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7841260	0.86[EUR][1000 genomes];0.80[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	nsv948343	chr8:64804219-65328394	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
2	nsv890969	chr8:64807144-65047353	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv890970	chr8:64975466-65125295	ZNF genes & repeats Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv534001	chr8:64992196-65798776	Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:64991600-64993400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr8:64992000-64993000	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr8:64992000-64993000	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr8:64992000-64993000	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr8:64992000-64993200	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr8:64992000-64993200	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr8:64992000-64993400	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr8:64992600-64993000	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr8:64992600-64993000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr8:64992600-64993000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr8:64992600-64993200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr8:64992800-64993000	Enhancers	H1 Cell Line	embryonic stem cell
13	chr8:64992800-64993000	Enhancers	H1 Derived Neuronal Progenitor 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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