Variant report

Variant	nsv605938
Chromosome Location	chr7:3792038-3852261
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:3793998..3797473-chr7:3798195..3801316,4	MCF-7	breast:
2	chr7:3800945..3803910-chr7:3805454..3807274,2	K562	blood:
3	chr7:3828320..3832262-chr7:3833106..3836337,3	K562	blood:
4	chr7:3848437..3851053-chr7:3868632..3870528,2	MCF-7	breast:
5	chr7:3824486..3827082-chr7:3833919..3835661,2	MCF-7	breast:
6	chr7:3450055..3452486-chr7:3794915..3797670,2	MCF-7	breast:
7	chr7:3801628..3804260-chr7:3804675..3806733,2	MCF-7	breast:
8	chr7:3800945..3803910-chr7:3805454..3807274,2	K562	blood:
9	chr7:3801628..3804260-chr7:3804675..3806733,2	MCF-7	breast:
10	chr7:3824486..3827082-chr7:3833919..3835661,2	MCF-7	breast:
11	chr7:3793998..3797473-chr7:3798195..3801316,4	MCF-7	breast:
12	chr7:3521823..3522640-chr7:3807742..3808264,2	MCF-7	breast:
13	chr7:3828320..3832262-chr7:3833106..3836337,3	K562	blood:

No data

Extended variants
information (count: 3523 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:3523 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7798663	chr7:3792038-3792039	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs10232141	chr7:3792041-3792042	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs150609483	chr7:3792148-3792149	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs578138441	chr7:3792179-3792180	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs114144161	chr7:3792234-3792235	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs560403330	chr7:3792258-3792259	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs573746075	chr7:3792278-3792279	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs542466283	chr7:3792299-3792300	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs562394575	chr7:3792305-3792306	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs531093665	chr7:3792351-3792352	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs113220476	chr7:3792353-3792354	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs550951405	chr7:3792382-3792383	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs187845946	chr7:3792395-3792396	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs549584614	chr7:3792407-3792408	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs527376584	chr7:3792428-3792429	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs117811928	chr7:3792449-3792450	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs149429204	chr7:3792482-3792483	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs6970269	chr7:3792484-3792485	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs144812810	chr7:3792491-3792492	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs139654703	chr7:3792560-3792561	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs538579790	chr7:3792571-3792572	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs558168547	chr7:3792612-3792613	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs577940332	chr7:3792620-3792621	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs192439400	chr7:3792636-3792637	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs371369756	chr7:3792645-3792646	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs574049944	chr7:3792655-3792656	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs542801624	chr7:3792658-3792659	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs76781988	chr7:3792660-3792661	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs144048109	chr7:3792680-3792681	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs185630855	chr7:3792698-3792699	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs564859941	chr7:3792708-3792709	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs188651614	chr7:3792713-3792714	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs527247843	chr7:3792736-3792737	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs540683327	chr7:3792764-3792765	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs560992093	chr7:3792778-3792779	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs193277595	chr7:3792795-3792796	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs79091400	chr7:3792821-3792822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs6951452	chr7:3792876-3792877	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs6975070	chr7:3792895-3792896	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs371701362	chr7:3792900-3792901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs372281962	chr7:3792907-3792908	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs184180765	chr7:3792912-3792913	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs145960209	chr7:3792949-3792950	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs534149809	chr7:3792950-3792951	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs553921597	chr7:3792981-3792982	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs188975353	chr7:3792982-3792983	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs139853161	chr7:3792998-3792999	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs371293540	chr7:3793003-3793004	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs555915969	chr7:3793004-3793005	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs181170548	chr7:3793013-3793014	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Chordoma	21602918	CNVD
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Developmental delay	21147756	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
Spondylocostal dysostosis	21085971	CNVD
Mental retardation	17901693	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	22286061	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
Colorectal cancer	21645411	CNVD
Intellectual disability	21811512	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Acute lymphoblastic leukemia	22237106	CNVD

Chromatin state (count:291 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:3773000-3820000	Weak transcription	Pancreas	Pancrea
2	chr7:3780200-3795400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr7:3782600-3800200	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr7:3788200-3794000	Weak transcription	Fetal Lung	lung
5	chr7:3789200-3793000	Weak transcription	Fetal Brain Male	brain
6	chr7:3790400-3794000	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr7:3791000-3793200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr7:3791600-3793600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr7:3791800-3793400	Enhancers	Primary neutrophils fromperipheralblood	blood
10	chr7:3792600-3792800	Enhancers	Gastric	stomach
11	chr7:3792800-3801800	Weak transcription	Gastric	stomach
12	chr7:3793000-3793200	Enhancers	Fetal Brain Male	brain
13	chr7:3793000-3793600	Enhancers	Fetal Brain Female	brain
14	chr7:3793000-3795000	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr7:3793000-3795000	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr7:3793200-3793800	Weak transcription	Fetal Brain Male	brain
17	chr7:3793200-3794000	Enhancers	Brain Anterior Caudate	brain
18	chr7:3793200-3794400	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr7:3793200-3794800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr7:3793200-3795000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr7:3793200-3795000	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr7:3793200-3795000	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr7:3793200-3795400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr7:3793400-3796600	Weak transcription	Primary neutrophils fromperipheralblood	blood
25	chr7:3793600-3794000	Enhancers	Brain Cingulate Gyrus	brain
26	chr7:3793600-3794000	Weak transcription	Fetal Brain Female	brain
27	chr7:3793600-3794200	Enhancers	Brain Germinal Matrix	brain
28	chr7:3793600-3794400	Enhancers	Cortex derived primary cultured neurospheres	brain
29	chr7:3793600-3794600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr7:3793600-3794800	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr7:3793600-3795000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr7:3793600-3795000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr7:3793600-3795600	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr7:3793800-3794000	Enhancers	Brain Hippocampus Middle	brain
35	chr7:3793800-3795000	Enhancers	Fetal Brain Male	brain
36	chr7:3794000-3794200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr7:3794000-3794200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr7:3794000-3794200	Flanking Active TSS	Brain Hippocampus Middle	brain
39	chr7:3794000-3794200	Enhancers	Brain Substantia Nigra	brain
40	chr7:3794000-3794200	Enhancers	Stomach Smooth Muscle	stomach
41	chr7:3794000-3794200	Enhancers	NH-A	brain
42	chr7:3794000-3794400	Flanking Active TSS	Brain Cingulate Gyrus	brain
43	chr7:3794000-3794400	Enhancers	Fetal Brain Female	brain
44	chr7:3794000-3794400	Enhancers	Fetal Heart	heart
45	chr7:3794000-3794400	Enhancers	Fetal Lung	lung
46	chr7:3794000-3795000	Enhancers	H1 Cell Line	embryonic stem cell
47	chr7:3794000-3795000	Active TSS	Duodenum Smooth Muscle	Duodenum
48	chr7:3794000-3795200	Active TSS	Brain Anterior Caudate	brain
49	chr7:3794000-3795200	Active TSS	Brain Inferior Temporal Lobe	brain
50	chr7:3794200-3794400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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