Variant report

Variant	rs2085251
Chromosome Location	chr8:63824941-63824942
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 66 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:63)

rs_ID	r²[population]
rs10092338	0.86[EUR][1000 genomes]
rs10102831	0.86[EUR][1000 genomes]
rs10107381	0.86[EUR][1000 genomes]
rs10282884	0.84[EUR][1000 genomes]
rs10282893	0.81[EUR][1000 genomes]
rs10504356	0.86[EUR][1000 genomes]
rs10504357	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs10504358	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs10504359	0.89[EUR][1000 genomes]
rs11989852	0.86[CHB][hapmap];0.81[JPT][hapmap]
rs11990678	0.88[CHB][hapmap];0.81[JPT][hapmap]
rs1480119	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs1600534	0.93[EUR][1000 genomes]
rs16929879	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17182014	1.00[CEU][hapmap];0.99[EUR][1000 genomes]
rs17194931	0.88[CHB][hapmap];0.81[JPT][hapmap]
rs17266243	0.88[EUR][1000 genomes]
rs17275944	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17279320	0.88[CHB][hapmap];0.81[JPT][hapmap]
rs17279355	0.86[CHB][hapmap];0.81[JPT][hapmap]
rs17279558	0.86[CHB][hapmap];0.81[JPT][hapmap]
rs1904571	0.90[EUR][1000 genomes]
rs2085253	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28387373	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs28494990	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28549153	0.84[EUR][1000 genomes]
rs28767608	0.99[EUR][1000 genomes]
rs28825674	0.84[EUR][1000 genomes]
rs28881312	0.84[EUR][1000 genomes]
rs3780127	0.86[CHB][hapmap];0.81[JPT][hapmap]
rs4636200	0.88[EUR][1000 genomes]
rs55641737	0.89[EUR][1000 genomes]
rs55919907	0.89[EUR][1000 genomes]
rs55933624	0.89[EUR][1000 genomes]
rs56047308	0.84[EUR][1000 genomes]
rs56252369	0.88[EUR][1000 genomes]
rs56653385	0.88[EUR][1000 genomes]
rs58210668	0.84[EUR][1000 genomes]
rs62508064	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62509402	0.81[EUR][1000 genomes]
rs62510765	0.88[EUR][1000 genomes]
rs62510766	0.84[EUR][1000 genomes]
rs62510767	0.88[EUR][1000 genomes]
rs62510768	0.88[EUR][1000 genomes]
rs62510770	0.88[EUR][1000 genomes]
rs62510778	0.90[EUR][1000 genomes]
rs62510779	0.90[EUR][1000 genomes]
rs62510780	0.90[EUR][1000 genomes]
rs62510781	0.90[EUR][1000 genomes]
rs62510782	0.90[EUR][1000 genomes]
rs62510783	0.93[EUR][1000 genomes]
rs62510825	0.89[EUR][1000 genomes]
rs62510826	0.89[EUR][1000 genomes]
rs62510836	0.99[EUR][1000 genomes]
rs6999540	0.90[EUR][1000 genomes]
rs7015302	0.88[CHB][hapmap];0.86[JPT][hapmap]
rs72653293	0.85[EUR][1000 genomes]
rs72653295	0.88[EUR][1000 genomes]
rs72653296	0.90[EUR][1000 genomes]
rs72653299	0.90[EUR][1000 genomes]
rs72655008	0.89[EUR][1000 genomes]
rs72655038	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9785076	0.84[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1018879	chr8:63281724-63937632	Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv831341	chr8:63658694-63852213	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1033527	chr8:63673915-64073735	Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs2085251	GGH	Cis_1M	lymphoblastoid	RTeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:63824800-63825400	Enhancers	Placenta	Placenta

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