Variant report

Variant	rs11916150
Chromosome Location	chr3:121667465-121667466
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs12695420	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13068522	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1474327	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1589700	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2091665	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2689276	0.87[AMR][1000 genomes]
rs2700424	0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3817599	0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4419417	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6438689	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6770115	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6780559	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7626740	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7628167	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7638094	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7647751	0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9289184	0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9289185	0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs953730	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9815649	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9828757	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9829181	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9843053	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv516233	chr3:121419301-121670405	Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Enhancers Genic enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
2	esv33139	chr3:121500400-122091831	Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs11916150	EAF2	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:121615800-121671600	Weak transcription	Pancreas	Pancrea
2	chr3:121635000-121670600	Weak transcription	Brain Hippocampus Middle	brain
3	chr3:121650600-121675600	Weak transcription	Brain Anterior Caudate	brain
4	chr3:121656800-121675200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr3:121660200-121670000	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr3:121660200-121671600	Weak transcription	Left Ventricle	heart
7	chr3:121660200-121675200	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr3:121660200-121676600	Weak transcription	Cortex derived primary cultured neurospheres	brain
9	chr3:121660600-121670400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr3:121661600-121670000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr3:121661800-121670200	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr3:121661800-121674800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr3:121662600-121669800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
14	chr3:121663200-121669400	Weak transcription	GM12878-XiMat	blood
15	chr3:121663200-121669800	Weak transcription	Primary B cells from peripheral blood	blood
16	chr3:121664000-121668000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr3:121664600-121670000	Weak transcription	Primary neutrophils fromperipheralblood	blood
18	chr3:121665200-121669400	Weak transcription	Primary monocytes fromperipheralblood	blood
19	chr3:121666000-121669600	Weak transcription	Primary B cells from cord blood	blood
20	chr3:121667200-121674400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr3:121667400-121667800	ZNF genes & repeats	Primary hematopoietic stem cells	blood
22	chr3:121667400-121670000	Strong transcription	Monocytes-CD14+_RO01746	blood

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