Variant report

Variant	rs1485506
Chromosome Location	chr8:65070952-65070953
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs10453088	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12056484	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12541027	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12542334	0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12542914	0.93[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12543669	0.97[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12545053	0.96[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12547267	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs13248130	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13251387	0.89[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs13253431	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs13254721	0.97[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs13256238	0.94[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs13274344	0.93[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs13280898	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1485510	0.93[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs17220928	0.96[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs17311772	0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs17311793	0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs17312403	0.97[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1867492	0.89[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2053644	0.94[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2053645	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2083996	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2083998	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2356339	0.97[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2883908	0.97[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs34054660	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs34337233	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs34927214	0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs35273528	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs35589320	0.89[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs35644708	0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs35836546	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs35946908	0.90[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs36026993	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4147347	0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs55985982	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs57568306	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs59234435	0.93[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs62521160	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6998317	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7828268	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7844990	0.96[AMR][1000 genomes];0.84[EUR][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	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
3	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
4	nsv890971	chr8:65028814-65242166	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:65060800-65074000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr8:65069600-65071800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
3	chr8:65069600-65072000	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chr8:65069800-65071800	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr8:65069800-65071800	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr8:65069800-65072200	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr8:65070000-65071000	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr8:65070000-65071800	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr8:65070000-65072000	Weak transcription	H1 Cell Line	embryonic stem cell

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