Variant report

Variant	rs7665652
Chromosome Location	chr4:151659452-151659453
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 93 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:83)

rs_ID	r²[population]
rs10008077	1.00[ASN][1000 genomes]
rs10025414	1.00[CEU][hapmap]
rs1148642	1.00[ASN][1000 genomes]
rs1201202	1.00[ASN][1000 genomes]
rs12645871	0.82[AFR][1000 genomes]
rs13126388	0.94[AFR][1000 genomes]
rs17027030	0.88[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];0.91[LWK][hapmap];1.00[MEX][hapmap];0.90[MKK][hapmap];1.00[TSI][hapmap];0.89[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17027034	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];0.82[MEX][hapmap];1.00[TSI][hapmap];0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17027100	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17027158	1.00[ASN][1000 genomes]
rs17440394	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1782360	1.00[CEU][hapmap]
rs1947314	0.89[AFR][1000 genomes]
rs2122920	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs294532	1.00[CEU][hapmap]
rs35879351	1.00[ASN][1000 genomes]
rs4355367	1.00[CEU][hapmap]
rs4431210	1.00[CEU][hapmap]
rs4533751	1.00[CEU][hapmap]
rs4696220	1.00[CEU][hapmap]
rs4696537	1.00[CEU][hapmap]
rs57218449	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57518605	1.00[ASN][1000 genomes]
rs58328072	1.00[ASN][1000 genomes]
rs59572961	1.00[ASN][1000 genomes]
rs60102523	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60391819	1.00[ASN][1000 genomes]
rs61258128	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61371689	1.00[ASN][1000 genomes]
rs61668839	1.00[ASN][1000 genomes]
rs62344564	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62344565	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62344567	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62344568	0.87[EUR][1000 genomes]
rs62344569	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62344571	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62344572	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62344573	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62344578	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62344579	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62344582	1.00[ASN][1000 genomes]
rs62344596	1.00[ASN][1000 genomes]
rs62344597	1.00[ASN][1000 genomes]
rs62344598	1.00[ASN][1000 genomes]
rs62344605	1.00[ASN][1000 genomes]
rs62346260	1.00[ASN][1000 genomes]
rs62346265	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62346268	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62346294	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62346295	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62346297	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62346301	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62346303	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62346304	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62346305	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62346306	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62346307	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62346308	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62346309	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62346311	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62346337	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62346338	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62346341	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62346345	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs62346346	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62346348	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62346349	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62346350	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62346351	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6535743	1.00[ASN][1000 genomes]
rs6535744	1.00[ASN][1000 genomes]
rs6819868	1.00[ASN][1000 genomes]
rs6836017	1.00[CEU][hapmap]
rs6841158	0.95[AFR][1000 genomes]
rs6847725	1.00[CEU][hapmap]
rs6854740	0.98[AFR][1000 genomes]
rs716474	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73859222	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73859291	1.00[ASN][1000 genomes]
rs73859295	1.00[ASN][1000 genomes]
rs7677186	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7698142	0.85[AFR][1000 genomes]
rs971640	0.88[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];0.98[LWK][hapmap];1.00[MEX][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];0.89[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv880256	chr4:151126725-151751369	Enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv817540	chr4:151228965-151858609	Strong transcription Active TSS Weak transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv869051	chr4:151347901-151737781	Strong transcription Weak transcription Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv1024820	chr4:151364078-151943561	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
5	nsv1032070	chr4:151514664-151775259	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv830113	chr4:151538184-151691942	Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
7	nsv1029861	chr4:151556384-151720601	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv1034948	chr4:151590115-152202687	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
9	nsv537302	chr4:151590115-152202687	ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
10	nsv530159	chr4:151624865-152203910	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:49 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:151639600-151671400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr4:151644400-151660800	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr4:151644400-151660800	Weak transcription	Aorta	Aorta
4	chr4:151644400-151663800	Weak transcription	HMEC	breast
5	chr4:151644600-151664200	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr4:151645200-151665800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
7	chr4:151645200-151671000	Weak transcription	Left Ventricle	heart
8	chr4:151645400-151695000	Weak transcription	Esophagus	oesophagus
9	chr4:151645600-151662600	Weak transcription	Pancreas	Pancrea
10	chr4:151645600-151669600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
11	chr4:151645600-151690400	Weak transcription	K562	blood
12	chr4:151645600-151749000	Weak transcription	Rectal Mucosa Donor 31	rectum
13	chr4:151647800-151677600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr4:151648000-151660800	Weak transcription	GM12878-XiMat	blood
15	chr4:151648000-151664000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr4:151648000-151676400	Weak transcription	Ovary	ovary
17	chr4:151648200-151703000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr4:151648600-151664800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr4:151650600-151666000	Weak transcription	Gastric	stomach
20	chr4:151652200-151660800	Weak transcription	Fetal Intestine Small	intestine
21	chr4:151652800-151659800	Weak transcription	Rectal Mucosa Donor 29	rectum
22	chr4:151652800-151661800	Weak transcription	Fetal Intestine Large	intestine
23	chr4:151653000-151663800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr4:151653000-151665400	Weak transcription	Dnd41	blood
25	chr4:151653000-151666000	Weak transcription	Duodenum Mucosa	Duodenum
26	chr4:151653000-151669600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
27	chr4:151653000-151683800	Weak transcription	Fetal Kidney	kidney
28	chr4:151653000-151692200	Weak transcription	Primary T cells fromperipheralblood	blood
29	chr4:151653000-151694400	Weak transcription	Thymus	Thymus
30	chr4:151653000-151749200	Weak transcription	Sigmoid Colon	Sigmoid Colon
31	chr4:151653200-151686000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr4:151653200-151690600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
33	chr4:151655000-151660800	Weak transcription	HUES6 Cell Line	embryonic stem cell
34	chr4:151655200-151660600	Weak transcription	HUES64 Cell Line	embryonic stem cell
35	chr4:151655200-151685400	Weak transcription	HSMMtube	muscle
36	chr4:151656000-151660800	Weak transcription	HUES48 Cell Line	embryonic stem cell
37	chr4:151656400-151667000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
38	chr4:151656400-151668400	Weak transcription	Primary B cells from peripheral blood	blood
39	chr4:151656400-151681600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
40	chr4:151656600-151663400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr4:151656600-151693400	Weak transcription	Primary T helper cells PMA-I stimulated	--
42	chr4:151656800-151671600	Weak transcription	Fetal Thymus	thymus
43	chr4:151657000-151663400	Weak transcription	Primary B cells from cord blood	blood
44	chr4:151657000-151668200	Weak transcription	Primary hematopoietic stem cells	blood
45	chr4:151657000-151668200	Weak transcription	Primary T helper cells fromperipheralblood	blood
46	chr4:151657000-151700600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
47	chr4:151657200-151666800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr4:151658400-151660600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr4:151658600-151668000	Weak transcription	Primary T cells from cord blood	blood

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