Variant report

Variant	rs9819224
Chromosome Location	chr3:139136519-139136520
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs1007079	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11919679	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1602627	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs182409	0.91[AMR][1000 genomes]
rs188419	0.96[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs192688	0.94[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs211581	0.92[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs211584	0.91[AMR][1000 genomes]
rs2233817	0.85[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2278577	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs295475	0.96[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs295476	0.96[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs295477	0.96[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs3772874	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs3772875	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs3821546	0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs60082560	0.96[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs60961550	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6439863	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6776315	0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72986799	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7373142	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7373302	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7648636	0.84[AFR][1000 genomes];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9858740	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9859683	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9879736	0.91[AMR][1000 genomes]
rs9879748	0.91[AMR][1000 genomes]
rs9882253	0.87[AFR][1000 genomes];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][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	nsv877543	chr3:139021139-139327261	Enhancers Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
2	nsv1003154	chr3:139060841-139788752	ZNF genes & repeats Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
3	nsv536729	chr3:139060841-139788752	Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
4	nsv949635	chr3:139091219-139367043	Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Enhancers Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:139114200-139153800	Weak transcription	Left Ventricle	heart
2	chr3:139131200-139142200	Weak transcription	Gastric	stomach
3	chr3:139132600-139137200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr3:139133200-139137000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr3:139133200-139144200	Weak transcription	Right Ventricle	heart
6	chr3:139133800-139140200	Weak transcription	Pancreas	Pancrea
7	chr3:139133800-139141200	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr3:139133800-139141800	Weak transcription	Ovary	ovary
9	chr3:139133800-139142200	Weak transcription	Brain Hippocampus Middle	brain
10	chr3:139133800-139144200	Weak transcription	Brain Anterior Caudate	brain
11	chr3:139134000-139142200	Weak transcription	Aorta	Aorta
12	chr3:139134200-139140200	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr3:139135800-139141800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
14	chr3:139136200-139141200	Weak transcription	Psoas Muscle	Psoas
15	chr3:139136400-139137000	Weak transcription	Fetal Stomach	stomach
16	chr3:139136400-139142200	Weak transcription	Brain Inferior Temporal Lobe	brain
17	chr3:139136400-139166200	Weak transcription	Fetal Brain Female	brain

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