Variant report

Variant	nsv1032112
Chromosome Location	chr9:25251849-25352691
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:11)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:25267661..25270080-chr9:25677540..25679201,2	MCF-7	breast:
2	chr9:25321931..25322446-chr9:25349957..25350559,2	MCF-7	breast:
3	chr9:24613953..24614528-chr9:25350122..25350850,2	MCF-7	breast:
4	chr9:25350133..25352434-chr9:25677647..25679713,3	MCF-7	breast:
5	chr9:25321931..25322446-chr9:25349957..25350559,2	MCF-7	breast:
6	chr9:25352690..25354379-chr9:25676635..25678931,2	MCF-7	breast:
7	chr9:25292451..25293431-chr9:25673511..25674229,2	MCF-7	breast:
8	chr9:25346387..25349185-chr9:25351167..25353046,2	MCF-7	breast:
9	chr9:25346387..25349185-chr9:25351167..25353046,2	MCF-7	breast:
10	chr9:25261310..25262090-chr9:25716255..25716920,2	MCF-7	breast:
11	chr9:25349920..25350511-chr9:25716130..25716944,2	MCF-7	breast:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TUSC1-1	chr9:25288488-25288555	NONHSAT130499
2	lnc-TUSC1-1	chr9:25290336-25290489	NONHSAT130499

No data

Variant related genes	Relation type
ENSG00000198680	chromatin interactions

Extended variants
information (count: 1525 )
Associated
traits (count: 147 )

Variant overlapped rSNPs/rCNVs (count:1525 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs35155120	chr9:25253206-25253207	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs564871530	chr9:25253210-25253211	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs183109518	chr9:25253227-25253228	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs547017165	chr9:25253232-25253233	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs1627255	chr9:25253254-25253255	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs529606894	chr9:25253255-25253256	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs549275153	chr9:25253283-25253284	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs569485529	chr9:25253318-25253319	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs55791649	chr9:25253334-25253335	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs551938794	chr9:25253344-25253345	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs147462960	chr9:25253361-25253362	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs534312820	chr9:25253369-25253370	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs554277002	chr9:25253372-25253373	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs73474171	chr9:25253386-25253387	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs80056763	chr9:25253402-25253403	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs566217724	chr9:25253408-25253409	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs375732573	chr9:25253420-25253421	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs556231874	chr9:25253450-25253451	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs539560764	chr9:25253508-25253509	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs140154972	chr9:25253541-25253542	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs7040877	chr9:25253580-25253581	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs1442852	chr9:25253633-25253634	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs571881313	chr9:25253650-25253651	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs540742308	chr9:25253659-25253660	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs7041019	chr9:25253685-25253686	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs529642568	chr9:25253709-25253710	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs1668966	chr9:25253717-25253718	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs563078303	chr9:25253782-25253783	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs189531329	chr9:25253784-25253785	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs551761090	chr9:25253824-25253825	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs571887514	chr9:25253854-25253855	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs534351835	chr9:25253867-25253868	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs182191122	chr9:25253927-25253928	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs567760602	chr9:25253928-25253929	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs187727195	chr9:25253932-25253933	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs556507095	chr9:25253945-25253946	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs576287448	chr9:25253963-25253964	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs538944624	chr9:25253986-25253987	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs1372870	chr9:25253996-25253997	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs192876241	chr9:25254060-25254061	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs540779180	chr9:25254125-25254126	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs368190466	chr9:25254143-25254144	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs560693744	chr9:25254145-25254146	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs574183036	chr9:25254150-25254151	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs144078368	chr9:25254230-25254231	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs563270976	chr9:25254245-25254246	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs531980092	chr9:25254270-25254271	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs183111275	chr9:25254347-25254348	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs552061586	chr9:25254363-25254364	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs150700351	chr9:25254390-25254391	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:147)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Melanoma	18172304	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	21668985	CNVD
Myelodysplastic syndrome	21251322	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	18803288	CNVD
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
Cancer	22183965	CNVD
Myelofibrosis	22110671	CNVD
Ewing''s sarcoma	22429812	CNVD
Neuroblastoma	21899760	CNVD
Glioblastoma multiforme	19435819	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Glioblastoma multiforme	22291905	CNVD
Lung cancer	21911935	CNVD
Primary central nervous system lymphoma	21088137	CNVD
head and neck squamous cell carcinoma	21798897	CNVD
Cancer	21253487	CNVD
Glioblastoma multiforme	22286061	CNVD
Intracranial ependymoma	16609018	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Urothelial cell carcinoma	18451213	CNVD
Glioma	17123091	CNVD
Mental retardation	17124404	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Acute lymphoblastic leukemia	18768390	CNVD
Leukemia	19602459	CNVD
Acute monocytic leukemia	16498392	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Leukemia	18688285	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Acute myeloid leukemia	19651601	CNVD
Coronary Disease	20032323	CNVD
Squamous cell cancer	20885788	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21732550	CNVD
Gastric cancer	22539939	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Metastatic melanoma	18483359	CNVD
Non-small cell lung cancer	20864512	CNVD
Cervical cancer	21062161	CNVD
Acute myeloid leukemia	16864856	CNVD
Glioblastoma	17090523	CNVD
Lung cancer	16773561	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16774939	CNVD
Bladder cancer	19088036	CNVD
Colorectal cancer	16272173	CNVD
Melanoma	16977458	CNVD
Glioblastoma multiforme	17369134	CNVD
Chagasic megaesophagus	20163722	CNVD
Melanoma	19566914	CNVD
Squamous cell cancer	19047905	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Adenoid cystic carcinoma	18332873	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21364760	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Lung cancer	21569311	CNVD
Pancreatic cancer	21811587	CNVD
early-passage human iPS cells	21368824	CNVD
Cancer	21215367	CNVD
Chordoma	21215367	CNVD
Bipolar disorder	19114987	CNVD
Non-small cell lung cancer	16651412	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:34 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:25253200-25254000	Enhancers	Fetal Brain Female	brain
2	chr9:25253400-25255800	Enhancers	Fetal Brain Male	brain
3	chr9:25254000-25254600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr9:25255000-25255400	Active TSS	HSMM	muscle
5	chr9:25259000-25260200	Enhancers	Fetal Kidney	kidney
6	chr9:25260200-25265000	Weak transcription	Fetal Kidney	kidney
7	chr9:25265000-25268000	Active TSS	Fetal Kidney	kidney
8	chr9:25266800-25267200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
9	chr9:25283600-25283800	Enhancers	Fetal Lung	lung
10	chr9:25283800-25284600	Weak transcription	Fetal Lung	lung
11	chr9:25284600-25285400	Enhancers	Fetal Lung	lung
12	chr9:25286600-25288200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr9:25287800-25288200	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr9:25288000-25288200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr9:25289200-25291200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr9:25291800-25292000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr9:25292000-25292400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr9:25292400-25295600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr9:25295400-25296200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr9:25295600-25296000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr9:25295600-25296000	Enhancers	Breast Myoepithelial Primary Cells	Breast
22	chr9:25310800-25312000	Enhancers	Fetal Brain Male	brain
23	chr9:25311000-25311400	Enhancers	Breast Myoepithelial Primary Cells	Breast
24	chr9:25311000-25311400	Enhancers	Adipose Nuclei	Adipose
25	chr9:25323400-25323800	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr9:25323800-25325400	Weak transcription	HUES48 Cell Line	embryonic stem cell
27	chr9:25325400-25325600	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr9:25325600-25326000	Weak transcription	HUES48 Cell Line	embryonic stem cell
29	chr9:25325800-25326200	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr9:25325800-25326200	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr9:25326000-25326400	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr9:25334400-25334600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr9:25347200-25348400	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr9:25350000-25350200	Enhancers	Fetal Brain Male	brain

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