Variant report

Variant	nsv1011020
Chromosome Location	chr2:33508811-33527784
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:33523300-33523527	K562	blood:	n/a	n/a
2	ATF1	chr2:33523272-33523602	K562	blood:	n/a	n/a
3	ATF3	chr2:33516228-33516950	A549	lung:	n/a	n/a
4	BCL3	chr2:33516373-33516960	A549	lung:	n/a	n/a
5	BCL3	chr2:33523207-33523469	GM12878	blood:	n/a	chr2:33523404-33523413 chr2:33523405-33523414
6	BCL3	chr2:33516117-33516981	A549	lung:	n/a	n/a
7	BHLHE40	chr2:33516464-33516665	HepG2	liver:	n/a	n/a
8	CEBPB	chr2:33523225-33523571	A549	lung:	n/a	n/a
9	CEBPB	chr2:33523152-33523596	IMR90	lung:	n/a	n/a
10	CEBPB	chr2:33518047-33518395	H1-hESC	embryonic stem cell:	n/a	chr2:33518207-33518216 chr2:33518205-33518218 chr2:33518207-33518216 chr2:33518206-33518217 chr2:33518207-33518216
11	CEBPB	chr2:33518099-33518389	MCF-7	breast:	n/a	chr2:33518207-33518216 chr2:33518205-33518218 chr2:33518207-33518216 chr2:33518206-33518217 chr2:33518207-33518216
12	CEBPB	chr2:33523192-33523623	A549	lung:	n/a	n/a
13	CEBPB	chr2:33518026-33518397	A549	lung:	n/a	chr2:33518207-33518216 chr2:33518205-33518218 chr2:33518207-33518216 chr2:33518206-33518217 chr2:33518207-33518216
14	CEBPB	chr2:33518086-33518365	Hela-S3	cervix:	n/a	chr2:33518207-33518216 chr2:33518205-33518218 chr2:33518207-33518216 chr2:33518206-33518217 chr2:33518207-33518216
15	CEBPB	chr2:33523259-33523568	K562	blood:	n/a	n/a
16	CEBPB	chr2:33523230-33523593	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr2:33518039-33518398	HepG2	liver:	n/a	chr2:33518207-33518216 chr2:33518205-33518218 chr2:33518207-33518216 chr2:33518206-33518217 chr2:33518207-33518216
18	CEBPB	chr2:33518624-33518643	A549	lung:	n/a	n/a
19	CEBPB	chr2:33518024-33518401	IMR90	lung:	n/a	chr2:33518207-33518216 chr2:33518205-33518218 chr2:33518207-33518216 chr2:33518206-33518217 chr2:33518207-33518216
20	CEBPB	chr2:33517954-33518506	A549	lung:	n/a	chr2:33518207-33518216 chr2:33518205-33518218 chr2:33518207-33518216 chr2:33518206-33518217 chr2:33518207-33518216
21	CEBPB	chr2:33518058-33518447	A549	lung:	n/a	chr2:33518207-33518216 chr2:33518205-33518218 chr2:33518207-33518216 chr2:33518206-33518217 chr2:33518207-33518216
22	CEBPB	chr2:33517995-33518337	K562	blood:	n/a	chr2:33518207-33518216 chr2:33518205-33518218 chr2:33518207-33518216 chr2:33518206-33518217 chr2:33518207-33518216
23	CEBPB	chr2:33518039-33518787	K562	blood:	n/a	chr2:33518755-33518766 chr2:33518207-33518216 chr2:33518205-33518218 chr2:33518756-33518768 chr2:33518207-33518216 chr2:33518206-33518217 chr2:33518207-33518216
24	CEBPB	chr2:33509508-33509698	A549	lung:	n/a	n/a
25	CEBPB	chr2:33523162-33523629	K562	blood:	n/a	n/a
26	CEBPB	chr2:33516274-33516922	A549	lung:	n/a	n/a
27	CEBPB	chr2:33527570-33527587	A549	lung:	n/a	chr2:33527571-33527584
28	CREB1	chr2:33516421-33516714	A549	lung:	n/a	n/a
29	CTCF	chr2:33511157-33511159	GM12878	blood:	n/a	n/a
30	CTCF	chr2:33511070-33511188	K562	blood:	n/a	chr2:33511124-33511140
31	CTCF	chr2:33515440-33515590	HepG2	liver:	n/a	n/a
32	E2F4	chr2:33516385-33516891	MCF10A-Er-Src	breast:	n/a	n/a
33	E2F4	chr2:33523166-33523494	MCF10A-Er-Src	breast:	n/a	n/a
34	EP300	chr2:33516376-33516781	HepG2	liver:	n/a	n/a
35	EP300	chr2:33522873-33523841	SK-N-SH	brain:	n/a	chr2:33523357-33523364
36	EP300	chr2:33516060-33517152	A549	lung:	n/a	chr2:33517010-33517024
37	EP300	chr2:33523243-33523507	SK-N-SH_RA	brain:	n/a	chr2:33523357-33523364
38	EP300	chr2:33523247-33523593	K562	blood:	n/a	chr2:33523357-33523364
39	EP300	chr2:33516163-33517059	A549	lung:	n/a	chr2:33517010-33517024
40	EP300	chr2:33516374-33516818	T-47D	breast:	n/a	n/a
41	EP300	chr2:33516342-33516629	SK-N-SH_RA	brain:	n/a	n/a
42	EP300	chr2:33516377-33516712	SK-N-SH_RA	brain:	n/a	n/a
43	EP300	chr2:33516178-33516955	SK-N-SH	brain:	n/a	n/a
44	EP300	chr2:33516367-33516777	HepG2	liver:	n/a	n/a
45	EP300	chr2:33516382-33516888	MCF-7	breast:	n/a	n/a
46	EP300	chr2:33513829-33514317	SK-N-SH	brain:	n/a	n/a
47	EP300	chr2:33518481-33518597	GM12878	blood:	n/a	n/a
48	EP300	chr2:33523188-33523586	SK-N-SH_RA	brain:	n/a	chr2:33523357-33523364
49	FOS	chr2:33516385-33516832	MCF10A-Er-Src	breast:	n/a	chr2:33516647-33516658
50	FOS	chr2:33523201-33523545	MCF10A-Er-Src	breast:	n/a	chr2:33523405-33523413 chr2:33523404-33523414 chr2:33523404-33523414

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:33518258-33518308	Hepatocyte	liver:	n/a
2	chr2:33518258-33518308	AG09309	skin:	n/a
3	chr2:33518258-33518308	HUVEC	blood vessel:	n/a
4	chr2:33518258-33518308	BJ	skin:	n/a
5	chr2:33518258-33518308	GM19239	blood:	n/a
6	chr2:33518258-33518308	HEEpiC	esophagus:	n/a
7	chr2:33518258-33518308	HCT-116	colon:	n/a
8	chr2:33518258-33518308	NH-A	brain:	n/a
9	chr2:33518258-33518308	U87	brain:	n/a
10	chr2:33518258-33518308	LNCaP	prostate:	n/a
11	chr2:33518258-33518308	ovcar-3	ovarian:	n/a
12	chr2:33518258-33518308	HPAEpiC	pulmonary alveolar:	n/a
13	chr2:33518258-33518308	HRCEpiC	kidney:	n/a
14	chr2:33518258-33518308	AoSMC	blood vessel:	n/a
15	chr2:33518258-33518308	ECC-1	luminal epithelium:	n/a
16	chr2:33518258-33518308	SK-N-MC	brain:	n/a
17	chr2:33518258-33518308	T-47D	breast:	n/a
18	chr2:33518258-33518308	AG10803	skin:	n/a
19	chr2:33518258-33518308	AG04449	skin:	fetal
20	chr2:33518258-33518308	PrEC	prostate:	n/a
21	chr2:33518258-33518308	HMEC	breast:	n/a
22	chr2:33518258-33518308	IMR90	lung:	fetal
23	chr2:33518258-33518308	AG09319	gingival:	n/a
24	chr2:33518258-33518308	HEK293	kidney:	embryo
25	chr2:33518258-33518308	PFSK-1	brain:	n/a
26	chr2:33518258-33518308	HNPCEpiC	eye:	n/a
27	chr2:33518258-33518308	HCF	heart:	n/a
28	chr2:33518258-33518308	HRE	kidney:	n/a
29	chr2:33518258-33518308	NHDF-neo	bronchial:	n/a
30	chr2:33518258-33518308	PANC-1	pancreas:	n/a
31	chr2:33518258-33518308	CMK	blood:	n/a
32	chr2:33518258-33518308	SKMC	muscle:	n/a
33	chr2:33518258-33518308	Hela-S3	cervix:	n/a
34	chr2:33518258-33518308	GM12878	blood:	n/a
35	chr2:33518258-33518308	HepG2	liver:	n/a
36	chr2:33518258-33518308	MCF10A-Er-Src	breast:	n/a
37	chr2:33518258-33518308	MCF-7	breast:	n/a
38	chr2:33518258-33518308	GM06990	blood:	n/a
39	chr2:33518258-33518308	HL-60	blood:	n/a
40	chr2:33518258-33518308	HCM	heart:	n/a
41	chr2:33518258-33518308	ProgFib	skin:	n/a
42	chr2:33518258-33518308	SK-N-SH_RA	brain:	n/a
43	chr2:33518258-33518308	GM12891	blood:	n/a
44	chr2:33518258-33518308	HRPEpiC	eye:	n/a
45	chr2:33518258-33518308	RPTEC	kidney:	n/a
46	chr2:33518258-33518308	Jurkat	blood:	n/a
47	chr2:33518258-33518308	SAEC	small airway:	n/a
48	chr2:33518258-33518308	Caco-2	colon:	n/a
49	chr2:33518258-33518308	H1-hESC	embryonic stem cell:	embryo
50	chr2:33518258-33518308	K562	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:33515586..33518253-chr2:33521124..33522863,2	MCF-7	breast:
2	chr2:33521500..33523864-chr2:33524061..33525573,2	K562	blood:
3	chr2:33508471..33509397-chr2:33534003..33534531,2	K562	blood:
4	chr2:33514697..33516578-chr2:33527291..33531093,3	MCF-7	breast:
5	chr2:33505710..33509161-chr2:33514931..33517884,3	K562	blood:
6	chr2:33513308..33515964-chr2:33519124..33522873,3	K562	blood:
7	chr2:33508125..33510502-chr2:33516735..33518824,2	K562	blood:
8	chr2:33514241..33517210-chr2:33520355..33523749,3	K562	blood:
9	chr2:33508125..33510502-chr2:33516735..33518824,2	K562	blood:
10	chr2:33521500..33523864-chr2:33524061..33525573,2	K562	blood:
11	chr2:33513308..33515964-chr2:33519124..33522873,3	K562	blood:

Variant related genes	Relation type
LTBP1	TF binding region
RNA5SP91	TF binding region
LTBP1	CpG island
RNA5SP91	CpG island
ENSG00000049323	chromatin interactions

Extended variants
information (count: 883 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:883 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs569565983	chr2:33508903-33508904	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs527630287	chr2:33508908-33508909	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs369502970	chr2:33508935-33508936	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs569213810	chr2:33508958-33508959	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs6719885	chr2:33508990-33508991	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs550155549	chr2:33509028-33509029	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs570225646	chr2:33509130-33509131	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs533658048	chr2:33509175-33509176	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs149149807	chr2:33509194-33509195	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs557946289	chr2:33509202-33509203	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs6722904	chr2:33509219-33509220	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs534018790	chr2:33509222-33509223	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs534566436	chr2:33509236-33509237	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs191557956	chr2:33509260-33509261	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs77871775	chr2:33509374-33509375	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs567072859	chr2:33509468-33509469	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs543500056	chr2:33509525-33509526	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs115187862	chr2:33509528-33509529	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs143237332	chr2:33509532-33509533	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs79394121	chr2:33509539-33509540	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs559191240	chr2:33509551-33509552	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs184335394	chr2:33509561-33509562	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs537546051	chr2:33509563-33509564	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs62148883	chr2:33509634-33509635	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs561333132	chr2:33509653-33509654	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs78082900	chr2:33509695-33509696	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs147401222	chr2:33509720-33509721	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs559053872	chr2:33509725-33509726	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs140479516	chr2:33509742-33509743	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs145816669	chr2:33509743-33509744	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs116736749	chr2:33509756-33509757	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs138435906	chr2:33509798-33509799	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs566411657	chr2:33509804-33509805	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs535315360	chr2:33509817-33509818	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs545991203	chr2:33509822-33509823	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs569720507	chr2:33509823-33509824	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs190069435	chr2:33509848-33509849	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs568036055	chr2:33509884-33509885	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs79865347	chr2:33509912-33509913	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs536756466	chr2:33509918-33509919	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs142940729	chr2:33509954-33509955	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs576646656	chr2:33509963-33509964	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs545557780	chr2:33509967-33509968	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs146165323	chr2:33509973-33509974	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs116420306	chr2:33509983-33509984	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs75167831	chr2:33509984-33509985	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs561138513	chr2:33509990-33509991	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs570948955	chr2:33510047-33510048	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs530060584	chr2:33510053-33510054	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs543574244	chr2:33510070-33510071	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Breast cancer	21364760	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	18927303	CNVD
Hereditary gingival fibromatosis	19633868	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Neurocytoma	17123091	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:495 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:33472000-33516600	Weak transcription	Psoas Muscle	Psoas
2	chr2:33487000-33509800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr2:33490600-33515600	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr2:33492000-33515800	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr2:33492200-33516600	Weak transcription	Brain Hippocampus Middle	brain
6	chr2:33492200-33516600	Weak transcription	Brain Substantia Nigra	brain
7	chr2:33492400-33547400	Weak transcription	Fetal Intestine Small	intestine
8	chr2:33493600-33515200	Weak transcription	Fetal Lung	lung
9	chr2:33493800-33515400	Weak transcription	Colon Smooth Muscle	Colon
10	chr2:33494200-33516000	Weak transcription	Rectal Smooth Muscle	rectum
11	chr2:33494200-33516200	Weak transcription	Fetal Kidney	kidney
12	chr2:33494600-33515200	Weak transcription	Duodenum Smooth Muscle	Duodenum
13	chr2:33501200-33511000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr2:33501200-33516400	Weak transcription	Stomach Mucosa	stomach
15	chr2:33501200-33528800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr2:33501400-33516600	Weak transcription	K562	blood
17	chr2:33501600-33509000	Weak transcription	HUVEC	blood vessel
18	chr2:33501800-33517800	Weak transcription	HUES64 Cell Line	embryonic stem cell
19	chr2:33502400-33512400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr2:33502400-33512600	Weak transcription	Lung	lung
21	chr2:33502400-33514000	Strong transcription	Osteobl	bone
22	chr2:33502400-33516000	Weak transcription	Brain Angular Gyrus	brain
23	chr2:33502400-33516600	Weak transcription	Pancreas	Pancrea
24	chr2:33502400-33516600	Weak transcription	Skeletal Muscle Male	skeletal muscle
25	chr2:33502400-33516800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr2:33502400-33516800	Weak transcription	Esophagus	oesophagus
27	chr2:33502600-33515200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
28	chr2:33502600-33515400	Weak transcription	NHDF-Ad	bronchial
29	chr2:33502600-33515800	Weak transcription	Skeletal Muscle Female	skeletal muscle
30	chr2:33502600-33537000	Weak transcription	Fetal Intestine Large	intestine
31	chr2:33503200-33515000	Weak transcription	Ovary	ovary
32	chr2:33503400-33515600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr2:33503600-33515400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr2:33503600-33518200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
35	chr2:33504000-33515800	Weak transcription	Fetal Brain Female	brain
36	chr2:33504200-33516000	Weak transcription	Fetal Brain Male	brain
37	chr2:33504400-33511800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr2:33505000-33526200	Weak transcription	Placenta	Placenta
39	chr2:33505400-33509200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr2:33505600-33512400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr2:33506200-33514400	Weak transcription	Fetal Stomach	stomach
42	chr2:33506400-33510200	Strong transcription	NH-A	brain
43	chr2:33506600-33509200	Weak transcription	NHLF	lung
44	chr2:33506800-33509000	Weak transcription	Cortex derived primary cultured neurospheres	brain
45	chr2:33506800-33509000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr2:33506800-33509400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr2:33506800-33509400	Weak transcription	Left Ventricle	heart
48	chr2:33506800-33514600	Weak transcription	Fetal Muscle Leg	muscle
49	chr2:33506800-33514800	Weak transcription	Aorta	Aorta
50	chr2:33506800-33515800	Weak transcription	Right Ventricle	heart

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links