Variant report

Variant	nsv459452
Chromosome Location	chr2:133841008-133875512
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	CEBPB	chr2:133862268-133862515	HepG2	liver:	n/a	n/a
2	CEBPB	chr2:133867453-133867754	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr2:133862217-133862515	IMR90	lung:	n/a	chr2:133862250-133862261 chr2:133862250-133862263
4	CEBPB	chr2:133862229-133862527	A549	lung:	n/a	chr2:133862250-133862261 chr2:133862250-133862263
5	CEBPB	chr2:133867421-133867772	IMR90	lung:	n/a	n/a
6	CTCF	chr2:133854730-133854822	MCF-7	breast:	n/a	n/a
7	CTCF	chr2:133854756-133854810	MCF-7	breast:	n/a	n/a
8	CTCF	chr2:133854760-133854910	SK-N-SH_RA	brain:	n/a	n/a
9	CTCF	chr2:133854739-133854794	MCF-7	breast:	n/a	n/a
10	CTCF	chr2:133854762-133854803	GM12892	blood:	n/a	n/a
11	CTCF	chr2:133847880-133848030	SK-N-SH_RA	brain:	n/a	n/a
12	CTCF	chr2:133854755-133854759	GM12892	blood:	n/a	n/a
13	CTCF	chr2:133854728-133854824	MCF-7	breast:	n/a	n/a
14	CTCF	chr2:133854738-133854797	A549	lung:	n/a	n/a
15	EP300	chr2:133843092-133843724	SK-N-SH_RA	brain:	n/a	n/a
16	EP300	chr2:133867309-133867793	SK-N-SH_RA	brain:	n/a	chr2:133867574-133867588 chr2:133867730-133867739
17	EP300	chr2:133867148-133867884	SK-N-SH	brain:	n/a	chr2:133867574-133867588 chr2:133867730-133867739
18	EP300	chr2:133842811-133844086	SK-N-SH	brain:	n/a	n/a
19	EP300	chr2:133847927-133848355	SK-N-SH_RA	brain:	n/a	chr2:133848310-133848320
20	EP300	chr2:133847641-133848608	SK-N-SH	brain:	n/a	chr2:133848310-133848320
21	EP300	chr2:133867196-133867948	SK-N-SH	brain:	n/a	chr2:133867574-133867588 chr2:133867730-133867739
22	EP300	chr2:133843072-133843763	SK-N-SH	brain:	n/a	n/a
23	EP300	chr2:133867233-133867793	SK-N-SH	brain:	n/a	chr2:133867574-133867588 chr2:133867730-133867739
24	EP300	chr2:133843036-133843677	SK-N-SH_RA	brain:	n/a	n/a
25	EP300	chr2:133847937-133848349	SK-N-SH_RA	brain:	n/a	chr2:133848310-133848320
26	EP300	chr2:133867285-133867761	SK-N-SH_RA	brain:	n/a	chr2:133867574-133867588 chr2:133867730-133867739
27	FOS	chr2:133867433-133867649	MCF10A-Er-Src	breast:	n/a	chr2:133867536-133867545
28	FOS	chr2:133867405-133867707	MCF10A-Er-Src	breast:	n/a	chr2:133867536-133867545
29	FOS	chr2:133867426-133867774	MCF10A-Er-Src	breast:	n/a	chr2:133867536-133867545
30	FOS	chr2:133867390-133867706	MCF10A-Er-Src	breast:	n/a	chr2:133867536-133867545
31	FOSL2	chr2:133867338-133867797	SK-N-SH	brain:	n/a	chr2:133867536-133867545
32	FOSL2	chr2:133843697-133844148	SK-N-SH	brain:	n/a	n/a
33	FOSL2	chr2:133867259-133867826	SK-N-SH	brain:	n/a	chr2:133867536-133867545
34	FOXA1	chr2:133845338-133845526	T-47D	breast:	n/a	n/a
35	FOXA1	chr2:133845275-133845589	T-47D	breast:	n/a	n/a
36	FOXM1	chr2:133867011-133867896	SK-N-SH	brain:	n/a	n/a
37	FOXM1	chr2:133867342-133867804	SK-N-SH	brain:	n/a	n/a
38	GATA2	chr2:133853427-133853775	SH-SY5Y	brain:	n/a	n/a
39	GATA2	chr2:133843160-133844074	SH-SY5Y	brain:	n/a	chr2:133843521-133843528 chr2:133843514-133843535 chr2:133843519-133843529 chr2:133843521-133843528 chr2:133843521-133843528 chr2:133843521-133843531 chr2:133843519-133843528
40	GATA3	chr2:133843201-133844170	SH-SY5Y	brain:	n/a	chr2:133843521-133843528 chr2:133843514-133843535 chr2:133843519-133843529 chr2:133843521-133843528 chr2:133843521-133843528 chr2:133843521-133843531 chr2:133843519-133843528
41	GATA3	chr2:133842976-133844330	SK-N-SH	brain:	n/a	chr2:133843521-133843528 chr2:133843514-133843535 chr2:133843519-133843529 chr2:133843521-133843528 chr2:133843521-133843528 chr2:133843521-133843531 chr2:133843519-133843528
42	GATA3	chr2:133867024-133867889	SK-N-SH	brain:	n/a	n/a
43	GATA3	chr2:133867238-133867910	SK-N-SH	brain:	n/a	n/a
44	GATA3	chr2:133843089-133844264	SK-N-SH	brain:	n/a	chr2:133843521-133843528 chr2:133843514-133843535 chr2:133843519-133843529 chr2:133843521-133843528 chr2:133843521-133843528 chr2:133843521-133843531 chr2:133843519-133843528
45	GATA3	chr2:133853425-133853800	SH-SY5Y	brain:	n/a	n/a
46	GATA3	chr2:133847901-133848327	SK-N-SH	brain:	n/a	n/a
47	GATA3	chr2:133866532-133866548	SH-SY5Y	brain:	n/a	n/a
48	JUN	chr2:133841803-133841985	HepG2	liver:	n/a	chr2:133841889-133841898 chr2:133841817-133841826 chr2:133841888-133841901
49	JUND	chr2:133867134-133867893	SK-N-SH	brain:	n/a	chr2:133867536-133867545
50	JUND	chr2:133841774-133842024	HepG2	liver:	n/a	chr2:133841889-133841898 chr2:133841817-133841826

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:133868449-133868499	HL-60	blood:	n/a
2	chr2:133855847-133855897	HAEpiC	amniotic membrane:	n/a
3	chr2:133868449-133868499	AG04449	skin:	fetal
4	chr2:133855847-133855897	GM06990	blood:	n/a
5	chr2:133855847-133855897	NH-A	brain:	n/a
6	chr2:133855847-133855897	GM12878	blood:	n/a
7	chr2:133868449-133868499	AG04450	lung:	fetal
8	chr2:133855847-133855897	BE2_C	brain:	n/a
9	chr2:133855847-133855897	MCF-7	breast:	n/a
10	chr2:133868449-133868499	HPAEpiC	pulmonary alveolar:	n/a
11	chr2:133855847-133855897	AG09319	gingival:	n/a
12	chr2:133855847-133855897	AG04450	lung:	fetal
13	chr2:133855847-133855897	HRCEpiC	kidney:	n/a
14	chr2:133855847-133855897	NHBE	bronchial:	n/a
15	chr2:133868449-133868499	ProgFib	skin:	n/a
16	chr2:133868449-133868499	GM12891	blood:	n/a
17	chr2:133868449-133868499	MCF10A-Er-Src	breast:	n/a
18	chr2:133868449-133868499	Hela-S3	cervix:	n/a
19	chr2:133855847-133855897	K562	blood:	n/a
20	chr2:133855847-133855897	LNCaP	prostate:	n/a
21	chr2:133855847-133855897	A549	lung:	n/a
22	chr2:133855847-133855897	AG09309	skin:	n/a
23	chr2:133855847-133855897	ECC-1	luminal epithelium:	n/a
24	chr2:133868449-133868499	K562	blood:	n/a
25	chr2:133868449-133868499	GM06990	blood:	n/a
26	chr2:133868449-133868499	PFSK-1	brain:	n/a
27	chr2:133855847-133855897	NT2-D1	testis:	n/a
28	chr2:133868449-133868499	HEEpiC	esophagus:	n/a
29	chr2:133868449-133868499	A549	lung:	n/a
30	chr2:133855847-133855897	HRE	kidney:	n/a
31	chr2:133855847-133855897	PFSK-1	brain:	n/a
32	chr2:133855847-133855897	H1-hESC	embryonic stem cell:	embryo
33	chr2:133855847-133855897	HL-60	blood:	n/a
34	chr2:133855847-133855897	NHDF-neo	bronchial:	n/a
35	chr2:133868449-133868499	HNPCEpiC	eye:	n/a
36	chr2:133855847-133855897	SK-N-MC	brain:	n/a
37	chr2:133855847-133855897	HPAEpiC	pulmonary alveolar:	n/a
38	chr2:133868449-133868499	GM12892	blood:	n/a
39	chr2:133855847-133855897	IMR90	lung:	fetal
40	chr2:133868449-133868499	NHDF-neo	bronchial:	n/a
41	chr2:133855847-133855897	CMK	blood:	n/a
42	chr2:133855847-133855897	NB4	blood:	n/a
43	chr2:133868449-133868499	H1-hESC	embryonic stem cell:	embryo
44	chr2:133855847-133855897	MCF10A-Er-Src	breast:	n/a
45	chr2:133868449-133868499	HRCEpiC	kidney:	n/a
46	chr2:133868449-133868499	MCF-7	breast:	n/a
47	chr2:133868449-133868499	HEK293	kidney:	embryo
48	chr2:133855847-133855897	AG04449	skin:	fetal
49	chr2:133868449-133868499	IMR90	lung:	fetal
50	chr2:133868449-133868499	HCM	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:133850084..133851752-chr2:133851774..133853791,2	MCF-7	breast:
2	chr2:133865556..133868534-chr2:133870878..133873548,2	K562	blood:
3	chr2:133811077..133813218-chr2:133838444..133841047,2	MCF-7	breast:
4	chr2:133865556..133868534-chr2:133870878..133873548,2	K562	blood:
5	chr2:133850171..133852489-chr2:133854080..133856768,2	MCF-7	breast:
6	chr2:133826353..133828506-chr2:133839741..133842653,2	MCF-7	breast:
7	chr2:133427195..133430167-chr2:133854644..133856509,2	MCF-7	breast:
8	chr2:133850171..133852489-chr2:133854080..133856768,2	MCF-7	breast:
9	chr2:133850084..133851752-chr2:133851774..133853791,2	MCF-7	breast:
10	chr2:133836968..133839255-chr2:133840150..133841905,2	K562	blood:

Variant related genes	Relation type
ENSG00000269686	TF binding region
ENSG00000269686	CpG island
ENSG00000150551	chromatin interactions

Extended variants
information (count: 1332 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:1332 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs375286337	chr2:133841008-133841009	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs539836997	chr2:133841017-133841018	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs66590303	chr2:133841029-133841030	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs573334273	chr2:133841051-133841052	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs190428915	chr2:133841090-133841091	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs555962455	chr2:133841166-133841167	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs530823010	chr2:133841174-133841175	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs183002652	chr2:133841193-133841194	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs16847317	chr2:133841199-133841200	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs147944997	chr2:133841255-133841256	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs140110116	chr2:133841296-133841297	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs145514160	chr2:133841324-133841325	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs544993946	chr2:133841357-133841358	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs187379705	chr2:133841358-133841359	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs72998839	chr2:133841359-133841360	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs527418901	chr2:133841361-133841362	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs76747255	chr2:133841385-133841386	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs561092587	chr2:133841403-133841404	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs113233181	chr2:133841413-133841414	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs549965885	chr2:133841454-133841455	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs115451435	chr2:133841455-133841456	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs147701862	chr2:133841491-133841492	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs75670198	chr2:133841492-133841493	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs566736922	chr2:133841501-133841502	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs74788147	chr2:133841510-133841511	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs113518098	chr2:133841520-133841521	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs192252534	chr2:133841534-133841535	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs557451065	chr2:133841549-133841550	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs538060129	chr2:133841590-133841591	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs149158518	chr2:133841647-133841648	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs578262702	chr2:133841706-133841707	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs367927981	chr2:133841710-133841711	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs34782758	chr2:133841717-133841718	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs536112877	chr2:133841722-133841723	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs575512170	chr2:133841727-133841728	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs183924485	chr2:133841834-133841835	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs142297170	chr2:133841849-133841850	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs531392554	chr2:133841910-133841911	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs557699577	chr2:133841929-133841930	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs543643904	chr2:133841934-133841935	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs569632816	chr2:133841952-133841953	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs10176860	chr2:133841981-133841982	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs188914566	chr2:133842085-133842086	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs192646894	chr2:133842113-133842114	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs565937133	chr2:133842143-133842144	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs184547103	chr2:133842152-133842153	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs548927713	chr2:133842154-133842155	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs151245306	chr2:133842184-133842185	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs73960009	chr2:133842187-133842188	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs556377648	chr2:133842228-133842229	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
lymphocytic leukemia	21291569	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Developmental delay	21147756	CNVD
Mental retardation	17621639	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Breast cancer	21509527	CNVD
Mental retardation	17124404	CNVD
Colorectal cancer	20459617	CNVD
Neuroticism	17667963	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	22522925	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:74 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:133831600-133855200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr2:133836200-133855200	Weak transcription	Ovary	ovary
3	chr2:133839800-133843600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr2:133841000-133854600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr2:133843600-133845400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr2:133844600-133845600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr2:133845400-133851600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr2:133845600-133848200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr2:133847000-133859200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr2:133848200-133848600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr2:133848200-133849000	Enhancers	NHDF-Ad	bronchial
12	chr2:133848400-133848600	Enhancers	Right Ventricle	heart
13	chr2:133848600-133854600	Weak transcription	Right Ventricle	heart
14	chr2:133849000-133849800	Weak transcription	NHDF-Ad	bronchial
15	chr2:133849800-133850600	Enhancers	NHDF-Ad	bronchial
16	chr2:133850000-133850600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr2:133850600-133855000	Weak transcription	NHDF-Ad	bronchial
18	chr2:133851600-133854600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr2:133853000-133867400	Weak transcription	Brain Hippocampus Middle	brain
20	chr2:133854600-133854800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr2:133854600-133854800	Enhancers	Left Ventricle	heart
22	chr2:133854600-133854800	Enhancers	Right Ventricle	heart
23	chr2:133854600-133865000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr2:133854800-133855200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr2:133854800-133892000	Weak transcription	Left Ventricle	heart
26	chr2:133855000-133855400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr2:133855000-133855400	Enhancers	NHDF-Ad	bronchial
28	chr2:133855200-133855400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr2:133855200-133855400	Enhancers	Ovary	ovary
30	chr2:133855200-133855600	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr2:133855200-133855800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr2:133855400-133855600	Flanking Active TSS	NHDF-Ad	bronchial
33	chr2:133855400-133856000	Active TSS	Ovary	ovary
34	chr2:133855400-133856200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr2:133855600-133855800	Enhancers	NHDF-Ad	bronchial
36	chr2:133855600-133856800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr2:133855600-133867800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr2:133855800-133856000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr2:133855800-133856000	Flanking Active TSS	NHDF-Ad	bronchial
40	chr2:133856000-133856600	Enhancers	NHDF-Ad	bronchial
41	chr2:133856000-133856800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr2:133856200-133857000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr2:133856600-133857600	Weak transcription	NHDF-Ad	bronchial
44	chr2:133857600-133857800	Enhancers	NHDF-Ad	bronchial
45	chr2:133859200-133859600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr2:133859600-133864800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr2:133862000-133863400	Enhancers	Fetal Lung	lung
48	chr2:133864000-133864800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr2:133864000-133865800	Enhancers	Fetal Brain Male	brain
50	chr2:133865000-133867800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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