Variant report

Variant	rs72635107
Chromosome Location	chr4:166590178-166590179
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs10012405	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10029541	0.88[ASN][1000 genomes]
rs11931542	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11932029	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11938725	0.92[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1246905	0.80[ASN][1000 genomes]
rs1246910	0.80[ASN][1000 genomes]
rs1246920	0.80[ASN][1000 genomes]
rs12650088	0.86[ASN][1000 genomes]
rs1312880	0.80[ASN][1000 genomes]
rs1459507	0.90[ASN][1000 genomes]
rs17632084	0.92[EUR][1000 genomes]
rs17632233	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1960435	0.80[ASN][1000 genomes]
rs2611205	0.86[ASN][1000 genomes]
rs2611209	0.84[ASN][1000 genomes]
rs2611211	0.83[ASN][1000 genomes]
rs2611212	0.84[ASN][1000 genomes]
rs2611214	0.84[ASN][1000 genomes]
rs2611218	0.84[ASN][1000 genomes]
rs2611220	0.84[ASN][1000 genomes]
rs2714831	0.84[ASN][1000 genomes]
rs2714835	0.84[ASN][1000 genomes]
rs2714836	0.84[ASN][1000 genomes]
rs28455937	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs28504666	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28602943	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4691212	0.99[ASN][1000 genomes]
rs55989211	0.87[EUR][1000 genomes]
rs56396842	1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs58230571	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60551091	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs61702512	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72631701	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72631702	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72635103	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72635104	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72635105	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72635106	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs736675	0.80[ASN][1000 genomes]
rs73863250	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73863253	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73863254	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7437622	0.84[ASN][1000 genomes]
rs764240	0.83[ASN][1000 genomes]
rs9308114	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9992610	1.00[EUR][1000 genomes];0.99[ASN][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	nsv830141	chr4:166502908-166689626	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv1028337	chr4:166544699-166659468	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv537338	chr4:166544699-166659468	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	esv3486584	chr4:166565013-166680227	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	esv3486585	chr4:166565013-166680227	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:166588600-166590200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr4:166589200-166590200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr4:166589600-166590200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr4:166589600-166590400	Enhancers	Muscle Satellite Cultured Cells	--
5	chr4:166589600-166590400	Enhancers	Fetal Heart	heart
6	chr4:166589600-166590400	Enhancers	HMEC	breast
7	chr4:166589800-166590200	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr4:166589800-166590200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr4:166589800-166590200	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr4:166589800-166590200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr4:166589800-166590200	Enhancers	Fetal Kidney	kidney
12	chr4:166589800-166590200	Enhancers	Right Atrium	heart
13	chr4:166589800-166590400	Enhancers	H1 Cell Line	embryonic stem cell
14	chr4:166589800-166590400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr4:166589800-166590400	Enhancers	H9 Cell Line	embryonic stem cell
16	chr4:166589800-166590400	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr4:166589800-166590400	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr4:166589800-166590400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr4:166589800-166590600	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr4:166590000-166591200	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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