Variant report

Variant	rs7430600
Chromosome Location	chr3:110856783-110856784
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:110856185..110858816-chr3:110868086..110870660,2	MCF-7	breast:

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

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs11717706	0.82[AFR][1000 genomes];0.86[AMR][1000 genomes]
rs11929280	0.85[CEU][hapmap]
rs13060876	0.81[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs13061640	0.81[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs13072462	0.82[AFR][1000 genomes];0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs13093206	0.99[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs1382075	0.81[AFR][1000 genomes]
rs1477841	1.00[CEU][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1477842	1.00[CEU][hapmap];0.86[YRI][hapmap];0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1477843	1.00[ASW][hapmap];1.00[CEU][hapmap];0.81[GIH][hapmap];0.86[LWK][hapmap];1.00[MEX][hapmap];1.00[YRI][hapmap];0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1477846	1.00[CEU][hapmap]
rs1477847	1.00[CEU][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1477848	1.00[CEU][hapmap]
rs1477851	1.00[ASW][hapmap];0.86[CEU][hapmap];1.00[LWK][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs1547518	0.80[AFR][1000 genomes];0.86[AMR][1000 genomes]
rs2126710	0.81[AFR][1000 genomes]
rs2126713	1.00[ASW][hapmap];1.00[CEU][hapmap];0.81[GIH][hapmap];0.96[LWK][hapmap];1.00[MEX][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.89[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs2169643	0.85[CEU][hapmap]
rs2399373	1.00[ASW][hapmap];1.00[CEU][hapmap];0.81[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.86[AMR][1000 genomes]
rs2399375	1.00[CEU][hapmap];0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs4682033	1.00[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs4682034	0.84[AFR][1000 genomes];0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4682229	1.00[ASW][hapmap];1.00[CEU][hapmap];0.80[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs4682230	1.00[ASW][hapmap];1.00[CEU][hapmap];0.81[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.86[AMR][1000 genomes]
rs4682231	1.00[CEU][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.86[AMR][1000 genomes]
rs4682234	1.00[ASW][hapmap];1.00[CEU][hapmap];0.80[GIH][hapmap];0.96[LWK][hapmap];1.00[MEX][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4682238	1.00[CEU][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs4682240	0.96[ASN][1000 genomes]
rs55774570	1.00[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs56668317	1.00[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs57417964	0.96[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs6437948	1.00[ASW][hapmap];1.00[CEU][hapmap];0.81[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6437952	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs6437953	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs6437955	0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs66803420	0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs67209183	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6781480	0.81[AFR][1000 genomes]
rs6786854	0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6794645	1.00[CEU][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs7433877	0.85[CEU][hapmap]
rs7610760	1.00[CEU][hapmap];0.93[YRI][hapmap];0.89[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs7612572	0.82[AFR][1000 genomes];0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7612667	0.82[ASW][hapmap];1.00[CEU][hapmap];0.81[GIH][hapmap];0.96[LWK][hapmap];1.00[MEX][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7623847	0.84[AFR][1000 genomes];0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7623880	1.00[CEU][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs7632375	0.81[AFR][1000 genomes]
rs7632388	0.81[AFR][1000 genomes]
rs7653595	1.00[CEU][hapmap];0.93[YRI][hapmap];0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs873132	0.85[CEU][hapmap]
rs9288918	0.85[CEU][hapmap]
rs9821335	0.94[ASW][hapmap];1.00[CEU][hapmap];0.81[GIH][hapmap];0.90[LWK][hapmap];1.00[MEX][hapmap];0.93[YRI][hapmap];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs9828899	1.00[ASW][hapmap];1.00[CEU][hapmap];0.81[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.86[AMR][1000 genomes]
rs9866028	1.00[ASW][hapmap];1.00[CEU][hapmap];0.81[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9876350	1.00[CEU][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.86[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1003106	chr3:110264476-111105943	Weak transcription Enhancers Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv460821	chr3:110637471-111501097	Enhancers Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv591275	chr3:110637471-111501097	Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
4	esv1850918	chr3:110685181-110889974	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv877338	chr3:110824425-110860188	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a
6	nsv1008308	chr3:110836281-110885834	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:52 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:110816000-110873800	Weak transcription	Left Ventricle	heart
2	chr3:110816000-110893400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr3:110819200-110857200	Weak transcription	NHLF	lung
4	chr3:110826800-110884200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr3:110829400-110893400	Weak transcription	HUVEC	blood vessel
6	chr3:110832200-110881800	Weak transcription	Small Intestine	intestine
7	chr3:110832200-110892400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr3:110832400-110911200	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr3:110834000-110891800	Weak transcription	Rectal Smooth Muscle	rectum
10	chr3:110835600-110929600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr3:110836200-110872800	Weak transcription	Rectal Mucosa Donor 29	rectum
12	chr3:110838400-110880200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr3:110842600-110911200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr3:110843000-110857400	Weak transcription	Adipose Nuclei	Adipose
15	chr3:110845400-110880000	Weak transcription	Fetal Kidney	kidney
16	chr3:110846000-110863600	Weak transcription	NHDF-Ad	bronchial
17	chr3:110847000-110873800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
18	chr3:110847000-110911400	Weak transcription	Fetal Muscle Leg	muscle
19	chr3:110847200-110873800	Weak transcription	Fetal Intestine Small	intestine
20	chr3:110847200-110874000	Weak transcription	Fetal Stomach	stomach
21	chr3:110848000-110872800	Weak transcription	Duodenum Smooth Muscle	Duodenum
22	chr3:110848000-110873800	Weak transcription	Fetal Intestine Large	intestine
23	chr3:110848200-110872600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr3:110848200-110891800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr3:110848400-110879800	Weak transcription	Placenta	Placenta
26	chr3:110852800-110857200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr3:110853000-110856800	Weak transcription	Placenta Amnion	Placenta Amnion
28	chr3:110853000-110860600	Weak transcription	Fetal Heart	heart
29	chr3:110853000-110872800	Weak transcription	Liver	Liver
30	chr3:110853000-110880000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr3:110853000-110919600	Weak transcription	Fetal Brain Male	brain
32	chr3:110853200-110865800	Weak transcription	Dnd41	blood
33	chr3:110853200-110866000	Weak transcription	HUES48 Cell Line	embryonic stem cell
34	chr3:110853200-110866400	Weak transcription	Muscle Satellite Cultured Cells	--
35	chr3:110853200-110867200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr3:110853200-110870000	Weak transcription	HUES6 Cell Line	embryonic stem cell
37	chr3:110853200-110870000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr3:110853200-110870600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
39	chr3:110853200-110873000	Weak transcription	A549	lung
40	chr3:110853200-110873800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr3:110853200-110880200	Weak transcription	Ovary	ovary
42	chr3:110853200-110897000	Weak transcription	H1 Cell Line	embryonic stem cell
43	chr3:110853200-110911000	Weak transcription	NH-A	brain
44	chr3:110853400-110866000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
45	chr3:110853400-110866000	Weak transcription	Fetal Lung	lung
46	chr3:110853400-110868000	Weak transcription	HUES64 Cell Line	embryonic stem cell
47	chr3:110853400-110870200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr3:110853400-110879800	Weak transcription	Duodenum Mucosa	Duodenum
49	chr3:110853800-110867200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr3:110853800-110869200	Weak transcription	HSMM	muscle

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