Variant report

Variant	rs61797634
Chromosome Location	chr3:120223562-120223563
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs1147719	0.81[ASN][1000 genomes]
rs1147721	0.90[ASN][1000 genomes]
rs11713908	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1259314	0.90[ASN][1000 genomes]
rs1259318	0.81[ASN][1000 genomes]
rs1259320	0.81[ASN][1000 genomes]
rs1259321	0.81[ASN][1000 genomes]
rs2319821	0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs34182414	0.94[ASN][1000 genomes]
rs3914889	0.96[ASN][1000 genomes]
rs4408894	0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4676792	0.94[ASN][1000 genomes]
rs4676793	0.94[ASN][1000 genomes]
rs5029440	0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs55662337	0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs55854851	0.94[ASN][1000 genomes]
rs61797633	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6438582	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6438583	0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6777371	0.80[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs8180105	0.92[ASN][1000 genomes]
rs8180108	0.94[ASN][1000 genomes]
rs9857229	0.94[ASN][1000 genomes]
rs9870449	0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1007557	chr3:119892894-120764353	Enhancers Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
2	nsv536706	chr3:119892894-120764353	Flanking Bivalent TSS/Enh Enhancers Active TSS Weak transcription Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
3	nsv1012127	chr3:120015620-120272893	Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
4	nsv536707	chr3:120015620-120272893	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
5	nsv1006428	chr3:120015620-120421982	Enhancers Strong transcription Weak transcription Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
6	esv3369381	chr3:120066425-120425510	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
7	esv3350409	chr3:120066445-120425480	Genic enhancers Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	33 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:120217000-120225200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr3:120217000-120225200	Weak transcription	Aorta	Aorta
3	chr3:120218000-120225000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr3:120218000-120225200	Weak transcription	Left Ventricle	heart
5	chr3:120218000-120225200	Weak transcription	Right Ventricle	heart
6	chr3:120218200-120226000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr3:120218600-120224600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr3:120219400-120224400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr3:120219400-120224600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr3:120219800-120225600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr3:120219800-120225800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr3:120222200-120223600	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
13	chr3:120222200-120224800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr3:120222400-120223600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
15	chr3:120222600-120223600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr3:120222600-120223600	Enhancers	Brain Germinal Matrix	brain
17	chr3:120222600-120223800	Enhancers	H1 Cell Line	embryonic stem cell
18	chr3:120223000-120223600	Enhancers	Fetal Brain Female	brain
19	chr3:120223200-120223600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr3:120223200-120223600	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr3:120223200-120223600	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr3:120223400-120223800	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr3:120223400-120225200	Weak transcription	Cortex derived primary cultured neurospheres	brain
24	chr3:120223400-120225800	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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