Variant report

Variant	rs10002207
Chromosome Location	chr4:120040351-120040352
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs10007353	0.89[EUR][1000 genomes]
rs10008206	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10011628	0.89[EUR][1000 genomes]
rs10011815	0.89[EUR][1000 genomes]
rs10017227	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10020251	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10027388	0.89[EUR][1000 genomes]
rs10027543	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10027649	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10027729	0.89[EUR][1000 genomes]
rs10033458	0.89[EUR][1000 genomes]
rs11934185	0.89[EUR][1000 genomes]
rs11934309	0.89[EUR][1000 genomes]
rs11935277	0.89[EUR][1000 genomes]
rs11935490	0.89[EUR][1000 genomes]
rs11936641	0.89[EUR][1000 genomes]
rs11943221	0.89[EUR][1000 genomes]
rs13434885	0.89[EUR][1000 genomes]
rs13435642	0.89[EUR][1000 genomes]
rs17050012	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17050027	0.89[EUR][1000 genomes]
rs17050032	0.89[EUR][1000 genomes]
rs17050065	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs17839092	0.89[EUR][1000 genomes]
rs2389726	0.89[EUR][1000 genomes]
rs28404363	0.89[EUR][1000 genomes]
rs28429127	0.89[EUR][1000 genomes]
rs28477374	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28480491	0.89[EUR][1000 genomes]
rs28507886	0.89[EUR][1000 genomes]
rs28526325	0.89[EUR][1000 genomes]
rs28682357	0.89[EUR][1000 genomes]
rs28687038	0.89[EUR][1000 genomes]
rs28691747	0.89[EUR][1000 genomes]
rs28734069	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4370120	0.89[EUR][1000 genomes]
rs4608795	0.89[EUR][1000 genomes]
rs56231990	0.87[EUR][1000 genomes]
rs72671701	0.83[AMR][1000 genomes]
rs72673713	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72673721	0.89[EUR][1000 genomes]
rs72673726	0.89[EUR][1000 genomes]
rs72673752	0.87[EUR][1000 genomes]
rs72673777	1.00[EUR][1000 genomes]
rs72673794	1.00[EUR][1000 genomes]
rs72676009	1.00[EUR][1000 genomes]
rs72676016	0.87[EUR][1000 genomes]
rs7666114	0.89[EUR][1000 genomes]
rs7666154	0.89[EUR][1000 genomes]
rs7666292	0.89[EUR][1000 genomes]
rs9307467	1.00[CEU][hapmap];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9996541	1.00[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916641	chr4:119780023-120777320	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
2	nsv948802	chr4:119844269-120208926	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
3	nsv1007214	chr4:120007913-120112460	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv1008115	chr4:120007913-120143849	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
5	nsv1003827	chr4:120008227-120112460	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv522386	chr4:120009147-120115379	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv1012868	chr4:120014630-120464880	Enhancers Flanking Active TSS Active TSS Weak transcription Genic enhancers ZNF genes & repeats Strong transcription 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	58 gene(s)	inside rSNPs	diseases
8	nsv537232	chr4:120014630-120464880	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
9	nsv1007619	chr4:120014898-120112460	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 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	chr4:120014800-120045000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr4:120034400-120044800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr4:120036600-120040600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr4:120037000-120046600	Weak transcription	Right Ventricle	heart
5	chr4:120037400-120040400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr4:120037600-120040800	Enhancers	HUVEC	blood vessel
7	chr4:120038400-120040400	Weak transcription	Left Ventricle	heart
8	chr4:120038400-120041800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr4:120038600-120043800	Weak transcription	HSMM	muscle
10	chr4:120038600-120044800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr4:120038600-120045000	Weak transcription	Aorta	Aorta
12	chr4:120038800-120045600	Weak transcription	Adipose Nuclei	Adipose
13	chr4:120039200-120040600	Enhancers	HMEC	breast
14	chr4:120039800-120044800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
15	chr4:120039800-120044800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr4:120039800-120044800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr4:120039800-120045000	Weak transcription	NHDF-Ad	bronchial
18	chr4:120040000-120041600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr4:120040000-120044800	Weak transcription	Primary hematopoietic stem cells	blood
20	chr4:120040000-120045400	Weak transcription	Osteobl	bone

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