Variant report

Variant	nsv1033537
Chromosome Location	chr9:2235700-2361750
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:36)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:2290959..2293717-chr9:2295989..2299437,4	MCF-7	breast:
2	chr9:2243537..2246838-chr9:2247520..2250621,4	MCF-7	breast:
3	chr9:2242145..2244162-chr9:2246197..2248614,2	MCF-7	breast:
4	chr9:2266333..2269283-chr9:2269848..2272589,2	K562	blood:
5	chr9:2335812..2338035-chr9:2341360..2343149,2	MCF-7	breast:
6	chr9:2335812..2338035-chr9:2341360..2343149,2	MCF-7	breast:
7	chr9:2016060..2018467-chr9:2241276..2243249,2	K562	blood:
8	chr9:2292225..2294051-chr9:2294141..2297013,2	MCF-7	breast:
9	chr9:2334689..2336340-chr9:2621369..2623518,2	MCF-7	breast:
10	chr9:2291871..2293597-chr9:2622079..2623974,2	MCF-7	breast:
11	chr9:2256748..2259220-chr9:2292192..2293911,2	MCF-7	breast:
12	chr9:2244966..2246945-chr9:2263682..2266605,2	MCF-7	breast:
13	chr9:2231807..2233920-chr9:2241447..2243691,2	MCF-7	breast:
14	chr9:2321723..2322570-chr9:2728160..2728820,2	MCF-7	breast:
15	chr9:2257367..2260216-chr9:2810940..2813820,2	MCF-7	breast:
16	chr9:2244966..2246945-chr9:2263682..2266605,2	MCF-7	breast:
17	chr9:2332261..2334098-chr9:2335447..2337175,2	MCF-7	breast:
18	chr9:2232135..2233681-chr9:2242107..2243678,2	MCF-7	breast:
19	chr9:2229721..2232093-chr9:2241469..2243158,2	MCF-7	breast:
20	chr9:2229879..2232148-chr9:2238435..2240178,2	K562	blood:
21	chr9:2256748..2259220-chr9:2292192..2293911,2	MCF-7	breast:
22	chr9:2242145..2244162-chr9:2246197..2248614,2	MCF-7	breast:
23	chr9:2266333..2269283-chr9:2269848..2272589,2	K562	blood:
24	chr9:2353709..2356767-chr9:2357162..2361529,4	K562	blood:
25	chr9:2255030..2255773-chr9:2600478..2601011,2	MCF-7	breast:
26	chr9:2226247..2228750-chr9:2234155..2236078,2	MCF-7	breast:
27	chr9:2353709..2356767-chr9:2357162..2361529,4	K562	blood:
28	chr9:2292225..2294051-chr9:2294141..2297013,2	MCF-7	breast:
29	chr9:2335749..2336338-chr9:2727775..2728597,3	MCF-7	breast:
30	chr9:2353709..2355330-chr9:2357162..2359493,2	K562	blood:
31	chr9:2332261..2334098-chr9:2335447..2337175,2	MCF-7	breast:
32	chr9:2290959..2293717-chr9:2295989..2299437,4	MCF-7	breast:
33	chr9:2240721..2243292-chr9:2621569..2623384,2	MCF-7	breast:
34	chr9:2243537..2246838-chr9:2247520..2250621,4	MCF-7	breast:
35	chr9:2333652..2336415-chr9:2621221..2622791,2	MCF-7	breast:
36	chr9:2353709..2355330-chr9:2357162..2359493,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SMARCA2-5	chr9:2264485-2264628	NONHSAT129991
2	lnc-SMARCA2-6	chr9:2287708-2288332	NONHSAT129989
3	lnc-SMARCA2-6	chr9:2291976-2293037	NONHSAT129989
4	lnc-SMARCA2-5	chr9:2273475-2274167	NONHSAT129991
5	lnc-SMARCA2-6	chr9:2276007-2276253	NONHSAT129989

No data

Variant related genes	Relation type
ENSG00000236404	chromatin interactions
ENSG00000147852	chromatin interactions
ENSG00000080503	chromatin interactions

Extended variants
information (count: 6355 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:6355 , 50 per page) page: 1 2 3 4 5 6 7 ... 128

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556241956	chr9:2235721-2235722	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs184948135	chr9:2235737-2235738	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs538106264	chr9:2235746-2235747	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs139769967	chr9:2235749-2235750	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs377482975	chr9:2235774-2235775	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs117887236	chr9:2235793-2235794	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs188933817	chr9:2235842-2235843	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs369126792	chr9:2235844-2235845	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs566990248	chr9:2235876-2235877	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs553872582	chr9:2235969-2235970	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs540097736	chr9:2235988-2235989	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs113313756	chr9:2235989-2235990	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs114947872	chr9:2236013-2236014	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs542609561	chr9:2236033-2236034	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs181564008	chr9:2236054-2236055	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs143586035	chr9:2236089-2236090	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs150559535	chr9:2236094-2236095	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs4740665	chr9:2236105-2236106	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs527925163	chr9:2236106-2236107	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs554281657	chr9:2236121-2236122	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs547663860	chr9:2236125-2236126	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs10118773	chr9:2236139-2236140	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs530111347	chr9:2236225-2236226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs117448059	chr9:2236257-2236258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs570102156	chr9:2236267-2236268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs577816464	chr9:2236268-2236269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs186099139	chr9:2236272-2236273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs551747051	chr9:2236281-2236282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs571557031	chr9:2236290-2236291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs534002368	chr9:2236307-2236308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs189390658	chr9:2236313-2236314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs6475625	chr9:2236315-2236316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs118144531	chr9:2236317-2236318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs113659512	chr9:2236320-2236321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs575660364	chr9:2236357-2236358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs149687157	chr9:2236371-2236372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs180743732	chr9:2236382-2236383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs186018419	chr9:2236409-2236410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs377594048	chr9:2236441-2236442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs541615308	chr9:2236444-2236445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs569919295	chr9:2236445-2236446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs561292148	chr9:2236456-2236457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs190939230	chr9:2236462-2236463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs183262996	chr9:2236526-2236527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs144513350	chr9:2236554-2236555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs113137028	chr9:2236580-2236581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs186358695	chr9:2236594-2236595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs571569021	chr9:2236624-2236625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs7854708	chr9:2236643-2236644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs190469060	chr9:2236672-2236673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Gastric cancer	16715143	CNVD
Glioblastoma multiforme	22286061	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Intracranial aneurysm	16715129	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Disorders of sex development	22290220	CNVD
Glioblastoma multiforme	21080181	CNVD
Sudden cardiac death	19188705	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	21952639	CNVD
Disorders of sex development	21048976	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
abnormal development	18461090	CNVD
Honadal dysgenesis	21048976	CNVD
Medulloblastoma	21979893	CNVD
Lung cancer	16740712	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Oral squamous cell carcinoma	17134496	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
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
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Autism	20531469	CNVD
XY gonadal dysgenesis	20685758	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Myelofibrosis	22110671	CNVD
Developmental delay	21373258	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Hepatocellular carcinoma	18803288	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1335 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:2223600-2240800	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr9:2230000-2241200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr9:2230200-2241200	Weak transcription	Stomach Mucosa	stomach
4	chr9:2231400-2235800	Enhancers	Fetal Heart	heart
5	chr9:2233600-2235800	Enhancers	Pancreatic Islets	Pancreatic Islet
6	chr9:2233800-2236200	Enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr9:2234400-2236000	Enhancers	Left Ventricle	heart
8	chr9:2234800-2237000	Weak transcription	Brain Germinal Matrix	brain
9	chr9:2235000-2237000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr9:2235000-2239600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr9:2235000-2240200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr9:2235000-2241200	Weak transcription	HMEC	breast
13	chr9:2235200-2239600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr9:2235200-2239800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr9:2235200-2240200	Weak transcription	Fetal Brain Female	brain
16	chr9:2235200-2241200	Weak transcription	NHEK	skin
17	chr9:2235200-2241400	Weak transcription	Right Ventricle	heart
18	chr9:2235400-2235800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr9:2235400-2241000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr9:2235400-2241200	Weak transcription	Fetal Muscle Trunk	muscle
21	chr9:2235400-2241400	Weak transcription	Esophagus	oesophagus
22	chr9:2235400-2241400	Weak transcription	Psoas Muscle	Psoas
23	chr9:2235600-2236000	Weak transcription	Fetal Muscle Leg	muscle
24	chr9:2235600-2237000	Weak transcription	Fetal Kidney	kidney
25	chr9:2235600-2239600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr9:2235600-2240000	Weak transcription	HUES6 Cell Line	embryonic stem cell
27	chr9:2235600-2240800	Weak transcription	Cortex derived primary cultured neurospheres	brain
28	chr9:2235600-2240800	Weak transcription	Fetal Brain Male	brain
29	chr9:2235600-2241000	Weak transcription	Fetal Lung	lung
30	chr9:2235600-2241000	Weak transcription	Fetal Stomach	stomach
31	chr9:2235600-2241400	Weak transcription	Colon Smooth Muscle	Colon
32	chr9:2235800-2237000	Weak transcription	Pancreatic Islets	Pancreatic Islet
33	chr9:2235800-2239800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr9:2235800-2241200	Weak transcription	Fetal Heart	heart
35	chr9:2236000-2241400	Weak transcription	Left Ventricle	heart
36	chr9:2236200-2241000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
37	chr9:2236800-2237000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr9:2237000-2237200	Active TSS	Pancreatic Islets	Pancreatic Islet
39	chr9:2237000-2237400	Enhancers	Brain Germinal Matrix	brain
40	chr9:2237000-2237600	Enhancers	Fetal Kidney	kidney
41	chr9:2237000-2238000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr9:2237000-2238600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr9:2237200-2237400	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
44	chr9:2237400-2239400	Enhancers	Pancreatic Islets	Pancreatic Islet
45	chr9:2237400-2241000	Weak transcription	Brain Germinal Matrix	brain
46	chr9:2237600-2241200	Weak transcription	Fetal Kidney	kidney
47	chr9:2238000-2242000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr9:2238600-2241000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr9:2239400-2241400	Weak transcription	Pancreatic Islets	Pancreatic Islet
50	chr9:2239600-2240200	Genic enhancers	ES-I3 Cell Line	embryonic stem cell

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