Variant report

Variant	rs7692328
Chromosome Location	chr4:120163756-120163757
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:120162306..120165092-chr4:120183039..120184970,2	K562	blood:

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs1033086	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1058450	1.00[YRI][hapmap]
rs1397606	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1397612	1.00[CEU][hapmap];0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1511020	1.00[CEU][hapmap];0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1511024	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs17050351	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs17050397	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs17050457	1.00[CEU][hapmap];0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2389744	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2389745	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4263382	1.00[ASN][1000 genomes]
rs4270572	1.00[ASN][1000 genomes]
rs4301093	1.00[ASN][1000 genomes]
rs4352459	1.00[ASN][1000 genomes]
rs4441740	1.00[ASN][1000 genomes]
rs4458436	1.00[CEU][hapmap];0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4611910	1.00[ASN][1000 genomes]
rs4834758	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4834763	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6534129	0.81[AMR][1000 genomes]
rs6814008	1.00[ASN][1000 genomes]
rs6818150	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6823192	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6833531	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6853132	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6853317	1.00[CEU][hapmap]
rs6853794	1.00[ASN][1000 genomes]
rs7658445	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7668809	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7668987	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7684673	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7690674	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9991222	1.00[CEU][hapmap];0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9998382	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 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	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
4	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
5	esv2763386	chr4:120143861-120186968	Strong transcription ZNF genes & repeats Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv461632	chr4:120158734-120180790	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv461633	chr4:120158734-120180790	Strong transcription Enhancers Genic enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv595332	chr4:120158734-120180790	Strong transcription Weak transcription Genic enhancers Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:104 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:120134800-120170000	Weak transcription	Colon Smooth Muscle	Colon
2	chr4:120135000-120170400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr4:120135000-120195800	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr4:120135200-120176200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr4:120135200-120176200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
6	chr4:120135400-120194600	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr4:120135600-120173800	Weak transcription	Brain Anterior Caudate	brain
8	chr4:120136200-120219200	Weak transcription	Brain Angular Gyrus	brain
9	chr4:120139400-120165800	Weak transcription	Fetal Kidney	kidney
10	chr4:120140600-120167400	Weak transcription	Colonic Mucosa	Colon
11	chr4:120141000-120192400	Weak transcription	Hela-S3	cervix
12	chr4:120143000-120167200	Weak transcription	Placenta	Placenta
13	chr4:120143000-120176200	Weak transcription	Esophagus	oesophagus
14	chr4:120143800-120167000	Weak transcription	Fetal Intestine Large	intestine
15	chr4:120146000-120178600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
16	chr4:120148200-120213600	Weak transcription	Fetal Muscle Leg	muscle
17	chr4:120152200-120167200	Weak transcription	Pancreas	Pancrea
18	chr4:120155000-120166200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
19	chr4:120155200-120167000	Weak transcription	NH-A	brain
20	chr4:120155400-120165200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr4:120155400-120165800	Weak transcription	Primary B cells from peripheral blood	blood
22	chr4:120155400-120166400	Weak transcription	Primary T helper cells fromperipheralblood	blood
23	chr4:120155400-120167200	Weak transcription	Aorta	Aorta
24	chr4:120155400-120167200	Weak transcription	Fetal Thymus	thymus
25	chr4:120155400-120167400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr4:120155400-120169800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
27	chr4:120155400-120169800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
28	chr4:120155400-120169800	Weak transcription	Ovary	ovary
29	chr4:120155400-120176200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr4:120155400-120176400	Weak transcription	Right Ventricle	heart
31	chr4:120155600-120165800	Weak transcription	HSMMtube	muscle
32	chr4:120155600-120169800	Weak transcription	Rectal Smooth Muscle	rectum
33	chr4:120155600-120173800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
34	chr4:120155600-120176400	Weak transcription	Brain Substantia Nigra	brain
35	chr4:120155600-120186000	Weak transcription	Fetal Heart	heart
36	chr4:120155800-120163800	Strong transcription	NHDF-Ad	bronchial
37	chr4:120156200-120165200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr4:120156200-120167200	Weak transcription	Psoas Muscle	Psoas
39	chr4:120156800-120167200	Weak transcription	Fetal Intestine Small	intestine
40	chr4:120156800-120167200	Weak transcription	Fetal Stomach	stomach
41	chr4:120157000-120170000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
42	chr4:120157600-120167000	Weak transcription	HepG2	liver
43	chr4:120157600-120176800	Weak transcription	Primary B cells from cord blood	blood
44	chr4:120157800-120165000	Weak transcription	Fetal Lung	lung
45	chr4:120157800-120167200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr4:120158000-120165200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr4:120158000-120165800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr4:120158000-120167000	Weak transcription	Stomach Smooth Muscle	stomach
49	chr4:120158000-120167200	Weak transcription	Duodenum Mucosa	Duodenum
50	chr4:120158000-120167200	Weak transcription	Lung	lung

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