Variant report

Variant	nsv892822
Chromosome Location	chr9:25295456-25396115
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:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:25352690..25354379-chr9:25676635..25678931,2	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	chr9:25346387..25349185-chr9:25351167..25353046,2	MCF-7	breast:
5	chr9:25350133..25352434-chr9:25677647..25679713,3	MCF-7	breast:
6	chr9:25346387..25349185-chr9:25351167..25353046,2	MCF-7	breast:
7	chr9:25349920..25350511-chr9:25716130..25716944,2	MCF-7	breast:
8	chr9:25321931..25322446-chr9:25349957..25350559,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000198680	chromatin interactions

Extended variants
information (count: 1056 )
Associated
traits (count: 145 )

Variant overlapped rSNPs/rCNVs (count:1056 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13287445	chr9:25295456-25295457	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs556642896	chr9:25295496-25295497	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs576713315	chr9:25295502-25295503	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs557441048	chr9:25295517-25295518	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs368097813	chr9:25295529-25295530	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs572472547	chr9:25295530-25295531	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs540246287	chr9:25295542-25295543	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs181186147	chr9:25295552-25295553	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs561558733	chr9:25295555-25295556	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs558250852	chr9:25295577-25295578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs572286372	chr9:25295585-25295586	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs541191251	chr9:25295610-25295611	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs147787997	chr9:25295634-25295635	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs530100209	chr9:25295680-25295681	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs552942451	chr9:25295697-25295698	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs563533147	chr9:25295732-25295733	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs532480099	chr9:25295770-25295771	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs35596992	chr9:25295792-25295793	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs552485762	chr9:25295796-25295797	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs141248838	chr9:25295809-25295810	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs75548632	chr9:25295834-25295835	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs548033260	chr9:25295859-25295860	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs184913993	chr9:25295871-25295872	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs146964177	chr9:25295874-25295875	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs556963126	chr9:25295913-25295914	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs144889434	chr9:25295921-25295922	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs371657424	chr9:25295925-25295926	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs189798232	chr9:25295929-25295930	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs558836186	chr9:25295970-25295971	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs571055774	chr9:25295973-25295974	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs533575064	chr9:25295985-25295986	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs181838006	chr9:25295994-25295995	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs111461673	chr9:25295995-25295996	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs541227537	chr9:25295999-25296000	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs376752897	chr9:25296009-25296010	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs561316270	chr9:25296100-25296101	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs149045702	chr9:25296102-25296103	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs186015698	chr9:25296139-25296140	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs190829417	chr9:25296188-25296189	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs563738837	chr9:25296189-25296190	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs527359532	chr9:25310807-25310808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs529343269	chr9:25310815-25310816	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs115900249	chr9:25310832-25310833	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs547156383	chr9:25310874-25310875	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs568603637	chr9:25310886-25310887	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs369878141	chr9:25310893-25310894	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs145313294	chr9:25310907-25310908	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs10757519	chr9:25310965-25310966	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs181711899	chr9:25310967-25310968	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs200714620	chr9:25310996-25310997	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:145)

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
Bipolar disorder	19114987	CNVD
Non-small cell lung cancer	16651412	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:55 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:25292400-25295600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr9:25295400-25296200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr9:25295600-25296000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr9:25295600-25296000	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr9:25310800-25312000	Enhancers	Fetal Brain Male	brain
6	chr9:25311000-25311400	Enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr9:25311000-25311400	Enhancers	Adipose Nuclei	Adipose
8	chr9:25323400-25323800	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr9:25323800-25325400	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr9:25325400-25325600	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr9:25325600-25326000	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr9:25325800-25326200	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr9:25325800-25326200	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr9:25326000-25326400	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr9:25334400-25334600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr9:25347200-25348400	Enhancers	Breast Myoepithelial Primary Cells	Breast
17	chr9:25350000-25350200	Enhancers	Fetal Brain Male	brain
18	chr9:25354400-25355400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
19	chr9:25357600-25358000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr9:25362600-25363000	Active TSS	Fetal Heart	heart
21	chr9:25376600-25377400	Enhancers	Skeletal Muscle Male	skeletal muscle
22	chr9:25377000-25377600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr9:25377000-25377600	Enhancers	Fetal Muscle Trunk	muscle
24	chr9:25377200-25377600	Enhancers	Psoas Muscle	Psoas
25	chr9:25379400-25379600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr9:25379600-25380600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr9:25380600-25381200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr9:25380600-25381200	Enhancers	Adipose Nuclei	Adipose
29	chr9:25380800-25381400	Enhancers	Fetal Lung	lung
30	chr9:25381200-25382000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr9:25381200-25383200	Weak transcription	Adipose Nuclei	Adipose
32	chr9:25382000-25382200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr9:25382200-25383400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr9:25383200-25383600	Enhancers	Adipose Nuclei	Adipose
35	chr9:25383400-25383600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr9:25385400-25385600	Enhancers	Adipose Nuclei	Adipose
37	chr9:25390000-25395400	Weak transcription	H1 Cell Line	embryonic stem cell
38	chr9:25393000-25393200	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr9:25393200-25394000	Weak transcription	HUES64 Cell Line	embryonic stem cell
40	chr9:25394000-25394800	Strong transcription	HUES64 Cell Line	embryonic stem cell
41	chr9:25394000-25396200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
42	chr9:25394200-25395000	Enhancers	Breast Myoepithelial Primary Cells	Breast
43	chr9:25394200-25396200	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
44	chr9:25394200-25396600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
45	chr9:25394400-25395400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
46	chr9:25394600-25399000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
47	chr9:25394800-25395600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
48	chr9:25395000-25395200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr9:25395000-25397400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
50	chr9:25395200-25396600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links