Variant report

Variant	rs6468900
Chromosome Location	chr8:104998775-104998776
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10112626	0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12675809	0.95[AFR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13248054	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13257910	0.88[EUR][1000 genomes]
rs13273017	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1603495	0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs17816262	0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1845928	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1954900	0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1954901	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1954905	0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2023029	0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4386947	0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4463386	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4467913	0.92[EUR][1000 genomes]
rs4549737	0.87[EUR][1000 genomes]
rs4618663	0.92[EUR][1000 genomes]
rs4734735	0.86[AFR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4734737	0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4734742	0.92[EUR][1000 genomes]
rs55959188	0.81[AFR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs57773033	0.83[AFR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62527146	0.90[EUR][1000 genomes]
rs6468895	0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6468896	0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6468897	0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6468899	0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6983436	0.82[AFR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6986875	0.82[AFR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6988613	0.88[CEU][hapmap];1.00[CHB][hapmap];0.84[JPT][hapmap]
rs6993567	0.96[AFR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7014986	0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7357535	0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7357566	0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7815854	0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7830448	0.96[AFR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7837318	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9692610	0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2752692	chr8:104520824-105123824	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv1031195	chr8:104601231-105194208	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
3	nsv831415	chr8:104907757-105115320	Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
4	nsv891248	chr8:104956705-105043211	Flanking Active TSS Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Active TSS	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
5	nsv465753	chr8:104956705-105136549	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
6	nsv611833	chr8:104956705-105136549	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
7	esv1824479	chr8:104961899-105032765	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
8	nsv891249	chr8:104963377-105077013	Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
9	nsv819897	chr8:104987702-105002005	Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:104992200-104999400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr8:104992800-105001600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr8:104993600-105000400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr8:104994400-105009200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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