Variant report

Variant	rs4327657
Chromosome Location	chr6:86207965-86207966
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:86203775..86205410-chr6:86207113..86209986,2	MCF-7	breast:
2	chr6:86207297..86209802-chr6:86213073..86214625,2	K562	blood:
3	chr6:86207507..86210473-chr6:86386895..86389586,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000203875	Chromatin interaction

Extended variants
information (count: 127 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:114)

rs_ID	r²[population]
rs1000632	0.81[ASN][1000 genomes]
rs1000633	0.81[ASN][1000 genomes]
rs1000634	0.81[ASN][1000 genomes]
rs11508041	0.82[ASN][1000 genomes]
rs11963844	0.82[ASN][1000 genomes]
rs11968230	0.82[ASN][1000 genomes]
rs11968238	0.82[ASN][1000 genomes]
rs12055597	0.81[ASN][1000 genomes]
rs12524836	0.85[ASN][1000 genomes]
rs12528808	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12662033	0.82[ASN][1000 genomes]
rs12664908	0.90[ASN][1000 genomes]
rs1322401	0.81[ASN][1000 genomes]
rs1570310	0.81[ASN][1000 genomes]
rs1570311	0.82[ASN][1000 genomes]
rs2208722	0.81[ASN][1000 genomes]
rs2229524	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2295890	0.82[ASN][1000 genomes]
rs3812137	1.00[ASN][1000 genomes]
rs3812139	0.96[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4144166	0.87[ASN][1000 genomes]
rs4144167	0.84[ASN][1000 genomes]
rs4373339	0.87[ASN][1000 genomes]
rs4400191	0.87[ASN][1000 genomes]
rs4458647	0.82[ASN][1000 genomes]
rs4463232	0.82[ASN][1000 genomes]
rs4487548	0.82[ASN][1000 genomes]
rs4565270	0.87[ASN][1000 genomes]
rs4571538	0.82[ASN][1000 genomes]
rs59744370	0.85[EUR][1000 genomes]
rs59797285	0.82[ASN][1000 genomes]
rs6900270	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6902638	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6902904	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6910543	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6913634	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6923017	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6930543	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6930790	0.93[ASN][1000 genomes]
rs6942065	0.87[ASN][1000 genomes]
rs73751215	1.00[ASN][1000 genomes]
rs7744309	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7746186	0.87[ASN][1000 genomes]
rs7749600	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7749745	0.81[ASN][1000 genomes]
rs7752105	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7753022	0.90[ASN][1000 genomes]
rs7753936	0.81[ASN][1000 genomes]
rs7753950	0.81[ASN][1000 genomes]
rs7754559	0.81[ASN][1000 genomes]
rs7771187	1.00[ASN][1000 genomes]
rs7771366	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7772233	0.82[ASN][1000 genomes]
rs7775788	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9294336	0.82[ASN][1000 genomes]
rs9342039	0.82[ASN][1000 genomes]
rs9344519	0.81[ASN][1000 genomes]
rs9344520	0.81[ASN][1000 genomes]
rs9344521	0.81[ASN][1000 genomes]
rs9344522	0.81[ASN][1000 genomes]
rs9344523	0.82[ASN][1000 genomes]
rs9344524	0.82[ASN][1000 genomes]
rs9344525	0.82[ASN][1000 genomes]
rs9344526	0.82[ASN][1000 genomes]
rs9344527	0.87[ASN][1000 genomes]
rs9344528	0.87[ASN][1000 genomes]
rs9344529	0.87[ASN][1000 genomes]
rs9344530	1.00[ASN][1000 genomes]
rs9344538	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9351063	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9351066	0.85[EUR][1000 genomes]
rs9353312	0.82[ASN][1000 genomes]
rs9353313	0.82[ASN][1000 genomes]
rs9353314	0.82[ASN][1000 genomes]
rs9353315	0.82[ASN][1000 genomes]
rs9353316	0.82[ASN][1000 genomes]
rs9353317	0.82[ASN][1000 genomes]
rs9353319	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9353321	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9353323	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9353324	0.95[EUR][1000 genomes]
rs9359654	0.82[ASN][1000 genomes]
rs9359655	0.87[ASN][1000 genomes]
rs9359656	0.93[ASN][1000 genomes]
rs9362211	0.81[ASN][1000 genomes]
rs9362213	0.81[ASN][1000 genomes]
rs9362215	0.81[ASN][1000 genomes]
rs9362216	0.82[ASN][1000 genomes]
rs9362217	0.82[ASN][1000 genomes]
rs9362218	0.82[ASN][1000 genomes]
rs9362219	0.82[ASN][1000 genomes]
rs9362220	0.82[ASN][1000 genomes]
rs9362221	0.82[ASN][1000 genomes]
rs9362223	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9362224	0.91[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs9362225	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9362226	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9444353	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9444356	0.95[EUR][1000 genomes]
rs9450274	0.82[ASN][1000 genomes]
rs9450278	0.82[ASN][1000 genomes]
rs9450279	0.82[ASN][1000 genomes]
rs9450280	0.87[ASN][1000 genomes]
rs9450286	1.00[ASN][1000 genomes]
rs9450289	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9450294	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9450295	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9450299	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9450300	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9450304	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9450307	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9450308	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9450309	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9450313	0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1017418	chr6:85344786-86259540	Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Enhancers Bivalent/Poised TSS Strong transcription Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	nsv538347	chr6:85344786-86259540	Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
3	nsv1022445	chr6:85972678-86392968	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	136 gene(s)	inside rSNPs	diseases
4	nsv538349	chr6:85972678-86392968	Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats 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	136 gene(s)	inside rSNPs	diseases
5	esv3326486	chr6:86020165-86292456	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
6	esv3435075	chr6:86052235-86271910	Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
7	nsv463937	chr6:86114766-86264374	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
8	nsv604092	chr6:86114766-86264374	Genic enhancers Flanking Active TSS Strong transcription Weak transcription Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
9	nsv520112	chr6:86144875-86247759	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
10	nsv886333	chr6:86199243-86289415	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
11	nsv463939	chr6:86205323-86279737	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
12	nsv470839	chr6:86205323-86279737	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
13	nsv604093	chr6:86205323-86279737	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs4327657	NT5E	cis	Thyroid	GTEx

Chromatin state (count:64 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:86176800-86242600	Weak transcription	Gastric	stomach
2	chr6:86186800-86211000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr6:86192800-86221400	Weak transcription	Brain Substantia Nigra	brain
4	chr6:86193000-86221200	Weak transcription	A549	lung
5	chr6:86193200-86212200	Weak transcription	Brain Anterior Caudate	brain
6	chr6:86193400-86208600	Weak transcription	HUVEC	blood vessel
7	chr6:86193400-86219800	Weak transcription	Brain Cingulate Gyrus	brain
8	chr6:86195000-86211800	Weak transcription	Duodenum Smooth Muscle	Duodenum
9	chr6:86195000-86219800	Weak transcription	Brain Angular Gyrus	brain
10	chr6:86196800-86221600	Weak transcription	Spleen	Spleen
11	chr6:86199600-86219400	Weak transcription	Skeletal Muscle Male	skeletal muscle
12	chr6:86200000-86219200	Weak transcription	Skeletal Muscle Female	skeletal muscle
13	chr6:86200200-86219400	Weak transcription	Colon Smooth Muscle	Colon
14	chr6:86200600-86208800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr6:86200600-86220400	Weak transcription	Psoas Muscle	Psoas
16	chr6:86200600-86221800	Weak transcription	Rectal Smooth Muscle	rectum
17	chr6:86200800-86212800	Weak transcription	Rectal Mucosa Donor 29	rectum
18	chr6:86201000-86216600	Weak transcription	Left Ventricle	heart
19	chr6:86201600-86218800	Weak transcription	Fetal Muscle Trunk	muscle
20	chr6:86202600-86212000	Weak transcription	Primary T cells from cord blood	blood
21	chr6:86202800-86208400	Weak transcription	Rectal Mucosa Donor 31	rectum
22	chr6:86202800-86211800	Weak transcription	Ovary	ovary
23	chr6:86202800-86218800	Weak transcription	Stomach Smooth Muscle	stomach
24	chr6:86203400-86219800	Weak transcription	NHLF	lung
25	chr6:86204800-86208000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr6:86204800-86208400	Weak transcription	NHEK	skin
27	chr6:86205000-86211000	Weak transcription	Adipose Nuclei	Adipose
28	chr6:86205000-86212400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr6:86205200-86208400	Weak transcription	Liver	Liver
30	chr6:86205200-86217600	Weak transcription	HSMMtube	muscle
31	chr6:86205200-86219600	Weak transcription	Placenta Amnion	Placenta Amnion
32	chr6:86205800-86208200	Weak transcription	HMEC	breast
33	chr6:86206000-86208600	Weak transcription	Muscle Satellite Cultured Cells	--
34	chr6:86206000-86212200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr6:86206000-86215200	Weak transcription	NHDF-Ad	bronchial
36	chr6:86206400-86212200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr6:86206800-86211200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr6:86207000-86208400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr6:86207000-86221600	Weak transcription	Lung	lung
40	chr6:86207200-86208400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr6:86207200-86217600	Weak transcription	Fetal Intestine Large	intestine
42	chr6:86207200-86219400	Weak transcription	Osteobl	bone
43	chr6:86207200-86219800	Weak transcription	Fetal Muscle Leg	muscle
44	chr6:86207200-86221200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr6:86207200-86221600	Weak transcription	Brain Germinal Matrix	brain
46	chr6:86207200-86238400	Weak transcription	Esophagus	oesophagus
47	chr6:86207400-86208400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr6:86207400-86208600	Strong transcription	Cortex derived primary cultured neurospheres	brain
49	chr6:86207400-86208600	Weak transcription	Duodenum Mucosa	Duodenum
50	chr6:86207400-86208600	Weak transcription	NH-A	brain

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