Variant report

Variant	rs7774848
Chromosome Location	chr6:119868386-119868387
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 49 )
Associated
traits (count: 1 )

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

rs_ID	r²[population]
rs10457355	0.80[CEU][hapmap]
rs10485004	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10485005	0.91[EUR][1000 genomes]
rs11153832	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12195793	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12197734	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12201876	0.92[EUR][1000 genomes]
rs12203478	0.91[EUR][1000 genomes]
rs12206086	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12206472	0.81[CEU][hapmap]
rs12207914	0.84[EUR][1000 genomes]
rs12208820	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12209160	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs13194194	0.91[EUR][1000 genomes]
rs13201608	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs13201736	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs13208284	0.91[EUR][1000 genomes]
rs13217373	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1499571	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs17628078	0.90[EUR][1000 genomes]
rs17628412	0.91[EUR][1000 genomes]
rs17628430	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs17628459	0.91[EUR][1000 genomes]
rs17628530	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2133533	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2153824	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs62418722	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs62418723	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62418738	0.83[EUR][1000 genomes]
rs62418739	0.83[EUR][1000 genomes]
rs66623281	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6899913	0.91[EUR][1000 genomes]
rs6918348	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6919823	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6923308	0.91[EUR][1000 genomes]
rs6923537	0.87[EUR][1000 genomes]
rs6923854	0.88[EUR][1000 genomes]
rs6927955	1.00[ASW][hapmap];1.00[CEU][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6935126	0.81[CEU][hapmap];0.81[MEX][hapmap]
rs72954953	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7743094	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7743821	0.91[EUR][1000 genomes]
rs7756933	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs870891	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3447598	chr6:119558591-120119384	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
2	esv3389526	chr6:119558598-120190087	ZNF genes & repeats Enhancers Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
3	nsv1027904	chr6:119709488-120001986	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	nsv533518	chr6:119712186-119998618	ZNF genes & repeats Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription	Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	esv3442553	chr6:119742069-120076777	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription	Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs7774848	FAM162B	cis	parietal	SCAN

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:119867800-119868400	Enhancers	iPS-18 Cell Line	embryonic stem cell
2	chr6:119867800-119868600	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr6:119868000-119868600	Enhancers	H9 Cell Line	embryonic stem cell
4	chr6:119868200-119868600	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr6:119868200-119868800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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