Variant report

Variant	nsv948851
Chromosome Location	chr2:133864452-133955999
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	chr2:133915573-133916005	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:133929022-133929350	HepG2	liver:	n/a	n/a
3	BATF	chr2:133892668-133892866	GM12878	blood:	n/a	n/a
4	BCL11A	chr2:133897445-133897743	H1-hESC	embryonic stem cell:	n/a	chr2:133897635-133897644 chr2:133897634-133897643
5	CEBPB	chr2:133927616-133927977	MCF-7	breast:	n/a	chr2:133927787-133927798 chr2:133927786-133927797 chr2:133927788-133927797
6	CEBPB	chr2:133911787-133911835	H1-hESC	embryonic stem cell:	n/a	chr2:133911792-133911803
7	CEBPB	chr2:133927438-133927952	A549	lung:	n/a	chr2:133927787-133927798 chr2:133927786-133927797 chr2:133927788-133927797
8	CEBPB	chr2:133911620-133911962	HepG2	liver:	n/a	chr2:133911792-133911803
9	CEBPB	chr2:133924811-133925135	IMR90	lung:	n/a	chr2:133924973-133924984
10	CEBPB	chr2:133888455-133888729	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr2:133927649-133927954	IMR90	lung:	n/a	chr2:133927787-133927798 chr2:133927786-133927797 chr2:133927788-133927797
12	CEBPB	chr2:133927644-133927947	MCF-7	breast:	n/a	chr2:133927787-133927798 chr2:133927786-133927797 chr2:133927788-133927797
13	CEBPB	chr2:133911686-133911964	MCF-7	breast:	n/a	chr2:133911792-133911803
14	CEBPB	chr2:133951727-133952071	A549	lung:	n/a	chr2:133951845-133951856
15	CEBPB	chr2:133951683-133952095	A549	lung:	n/a	chr2:133951845-133951856
16	CEBPB	chr2:133884649-133884917	IMR90	lung:	n/a	chr2:133884879-133884890 chr2:133884881-133884890
17	CEBPB	chr2:133884617-133885020	HepG2	liver:	n/a	chr2:133884879-133884890 chr2:133884881-133884890
18	CEBPB	chr2:133888428-133888781	IMR90	lung:	n/a	n/a
19	CEBPB	chr2:133867453-133867754	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr2:133927441-133927955	HepG2	liver:	n/a	chr2:133927787-133927798 chr2:133927786-133927797 chr2:133927788-133927797
21	CEBPB	chr2:133951704-133952046	HepG2	liver:	n/a	chr2:133951845-133951856
22	CEBPB	chr2:133867421-133867772	IMR90	lung:	n/a	n/a
23	CEBPB	chr2:133897405-133897664	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr2:133951548-133952193	A549	lung:	n/a	chr2:133951845-133951856
25	CEBPB	chr2:133951692-133952052	IMR90	lung:	n/a	chr2:133951845-133951856
26	CEBPB	chr2:133911651-133911930	IMR90	lung:	n/a	chr2:133911792-133911803
27	CEBPB	chr2:133927773-133927830	H1-hESC	embryonic stem cell:	n/a	chr2:133927787-133927798 chr2:133927786-133927797 chr2:133927788-133927797
28	CEBPB	chr2:133911687-133911964	A549	lung:	n/a	chr2:133911792-133911803
29	CEBPB	chr2:133924899-133925138	A549	lung:	n/a	chr2:133924973-133924984
30	CEBPB	chr2:133923387-133923427	HepG2	liver:	n/a	n/a
31	CEBPB	chr2:133924821-133925142	HepG2	liver:	n/a	chr2:133924973-133924984
32	CEBPB	chr2:133927367-133927908	Hela-S3	cervix:	n/a	chr2:133927787-133927798 chr2:133927786-133927797 chr2:133927788-133927797
33	CEBPB	chr2:133951657-133952062	Hela-S3	cervix:	n/a	chr2:133951845-133951856
34	CEBPB	chr2:133911637-133911956	Hela-S3	cervix:	n/a	chr2:133911792-133911803
35	CHD2	chr2:133897550-133897741	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr2:133928740-133928890	GM12873	blood:	n/a	n/a
37	CTCF	chr2:133929080-133929230	HBMEC	blood vessel:	n/a	chr2:133929165-133929181 chr2:133929164-133929182 chr2:133929166-133929179 chr2:133929159-133929180
38	CTCF	chr2:133929100-133929250	AG09319	gingival:	n/a	chr2:133929165-133929181 chr2:133929164-133929182 chr2:133929166-133929179 chr2:133929159-133929180
39	CTCF	chr2:133928640-133929575	SK-N-SH	brain:	n/a	chr2:133929165-133929181 chr2:133929164-133929182 chr2:133929166-133929179 chr2:133929159-133929180
40	CTCF	chr2:133949680-133949830	HPF	lung:	n/a	n/a
41	CTCF	chr2:133929140-133929290	HVMF	connective:	n/a	chr2:133929165-133929181 chr2:133929164-133929182 chr2:133929166-133929179 chr2:133929159-133929180
42	CTCF	chr2:133904620-133904770	HCPEpiC	choroid plexus:	n/a	chr2:133904676-133904697
43	CTCF	chr2:133949780-133949930	Caco-2	colon:	n/a	n/a
44	CTCF	chr2:133929080-133929230	HPAF	blood vessel:	n/a	chr2:133929165-133929181 chr2:133929164-133929182 chr2:133929166-133929179 chr2:133929159-133929180
45	CTCF	chr2:133929120-133929270	WERI-Rb-1	eye:	n/a	chr2:133929165-133929181 chr2:133929164-133929182 chr2:133929166-133929179 chr2:133929159-133929180
46	CTCF	chr2:133929100-133929250	GM12869	blood:	n/a	chr2:133929165-133929181 chr2:133929164-133929182 chr2:133929166-133929179 chr2:133929159-133929180
47	CTCF	chr2:133949700-133949850	MCF-7	breast:	n/a	n/a
48	CTCF	chr2:133929060-133929210	GM12875	blood:	n/a	chr2:133929165-133929181 chr2:133929164-133929182 chr2:133929166-133929179 chr2:133929159-133929180
49	CTCF	chr2:133929100-133929250	AG04449	skin:	n/a	chr2:133929165-133929181 chr2:133929164-133929182 chr2:133929166-133929179 chr2:133929159-133929180
50	CTCF	chr2:133929040-133929190	A549	lung:	n/a	chr2:133929165-133929181 chr2:133929164-133929182 chr2:133929166-133929179 chr2:133929159-133929180

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:133927261-133927311	AG04450	lung:	fetal
2	chr2:133927261-133927311	AG04450	lung:	fetal
3	chr2:133934804-133934854	PANC-1	pancreas:	n/a
4	chr2:133923604-133923654	GM06990	blood:	n/a
5	chr2:133888263-133888313	HMEC	breast:	n/a
6	chr2:133923604-133923654	AoSMC	blood vessel:	n/a
7	chr2:133888263-133888313	MCF-7	breast:	n/a
8	chr2:133868449-133868499	BJ	skin:	n/a
9	chr2:133888263-133888313	HEK293	kidney:	embryo
10	chr2:133868449-133868499	PrEC	prostate:	n/a
11	chr2:133927261-133927311	HCM	heart:	n/a
12	chr2:133927261-133927311	CMK	blood:	n/a
13	chr2:133927261-133927311	NHDF-neo	bronchial:	n/a
14	chr2:133888263-133888313	HRPEpiC	eye:	n/a
15	chr2:133923604-133923654	ovcar-3	ovarian:	n/a
16	chr2:133927261-133927311	GM19239	blood:	n/a
17	chr2:133923604-133923654	NHBE	bronchial:	n/a
18	chr2:133923604-133923654	PANC-1	pancreas:	n/a
19	chr2:133934804-133934854	HCM	heart:	n/a
20	chr2:133923604-133923654	AG09309	skin:	n/a
21	chr2:133927261-133927311	MCF10A-Er-Src	breast:	n/a
22	chr2:133888263-133888313	AG10803	skin:	n/a
23	chr2:133927261-133927311	HRPEpiC	eye:	n/a
24	chr2:133888263-133888313	MCF10A-Er-Src	breast:	n/a
25	chr2:133923604-133923654	HCM	heart:	n/a
26	chr2:133923604-133923654	GM19239	blood:	n/a
27	chr2:133927261-133927311	Hepatocyte	liver:	n/a
28	chr2:133934804-133934854	GM19239	blood:	n/a
29	chr2:133868449-133868499	SKMC	muscle:	n/a
30	chr2:133888263-133888313	Hela-S3	cervix:	n/a
31	chr2:133868449-133868499	Jurkat	blood:	n/a
32	chr2:133888263-133888313	SKMC	muscle:	n/a
33	chr2:133934804-133934854	BE2_C	brain:	n/a
34	chr2:133868449-133868499	NHDF-neo	bronchial:	n/a
35	chr2:133923604-133923654	GM12892	blood:	n/a
36	chr2:133934804-133934854	HCF	heart:	n/a
37	chr2:133927261-133927311	HRE	kidney:	n/a
38	chr2:133934804-133934854	HPAEpiC	pulmonary alveolar:	n/a
39	chr2:133927261-133927311	LNCaP	prostate:	n/a
40	chr2:133923604-133923654	LNCaP	prostate:	n/a
41	chr2:133923604-133923654	Hepatocyte	liver:	n/a
42	chr2:133934804-133934854	ProgFib	skin:	n/a
43	chr2:133868449-133868499	SAEC	small airway:	n/a
44	chr2:133888263-133888313	PrEC	prostate:	n/a
45	chr2:133923604-133923654	RPTEC	kidney:	n/a
46	chr2:133923604-133923654	HRCEpiC	kidney:	n/a
47	chr2:133888263-133888313	K562	blood:	n/a
48	chr2:133923604-133923654	PrEC	prostate:	n/a
49	chr2:133927261-133927311	Caco-2	colon:	n/a
50	chr2:133934804-133934854	HCPEpiC	choroid plexus:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:133408307..133409298-chr2:133928740..133929575,3	MCF-7	breast:
2	chr2:133106208..133106974-chr2:133928762..133929385,2	MCF-7	breast:
3	chr2:133426638..133429342-chr2:133954852..133957761,2	MCF-7	breast:
4	chr2:133304640..133305382-chr2:133928983..133929651,2	MCF-7	breast:
5	chr2:133907650..133909821-chr2:133911613..133914505,3	MCF-7	breast:
6	chr2:133865556..133868534-chr2:133870878..133873548,2	K562	blood:
7	chr2:133427423..133430466-chr2:133927227..133930556,4	MCF-7	breast:
8	chr2:133932748..133934866-chr2:133936195..133938875,2	MCF-7	breast:
9	chr2:133428080..133428797-chr2:133928852..133929367,2	MCF-7	breast:
10	chr2:133953064..133954873-chr2:134023809..134025378,2	MCF-7	breast:
11	chr2:133922662..133923182-chr20:49410946..49412118,12	MCF-7	breast:
12	chr2:133907650..133909821-chr2:133911613..133914505,3	MCF-7	breast:
13	chr2:133922662..133923182-chr20:49410992..49411888,4	MCF-7	breast:
14	chr2:133434344..133435258-chr2:133928761..133929306,2	MCF-7	breast:
15	chr2:133426257..133428194-chr2:133927974..133930516,2	MCF-7	breast:
16	chr2:133865556..133868534-chr2:133870878..133873548,2	K562	blood:
17	chr2:133304031..133305145-chr2:133928594..133929580,6	MCF-7	breast:
18	chr2:133932748..133934866-chr2:133936195..133938875,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000269686	TF binding region
ENSG00000269686	CpG island
ENSG00000150551	chromatin interactions
ENSG00000124243	chromatin interactions
ENSG00000226953	chromatin interactions

Extended variants
information (count: 3380 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:3380 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4437017	chr2:133864452-133864453	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs552705186	chr2:133864455-133864456	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs570917897	chr2:133864503-133864504	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs558888081	chr2:133864525-133864526	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs553514910	chr2:133864574-133864575	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs575057510	chr2:133864599-133864600	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs78993445	chr2:133864651-133864652	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs149888940	chr2:133864700-133864701	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs181003434	chr2:133864715-133864716	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs545347386	chr2:133864718-133864719	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs144897615	chr2:133864738-133864739	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs75429750	chr2:133864783-133864784	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs540089608	chr2:133864801-133864802	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs561901161	chr2:133864864-133864865	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs529073027	chr2:133864879-133864880	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs114839379	chr2:133864937-133864938	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs562734460	chr2:133864941-133864942	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs537599404	chr2:133864947-133864948	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs16848067	chr2:133864994-133864995	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs565179542	chr2:133865016-133865017	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs552530651	chr2:133865018-133865019	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs185628185	chr2:133865026-133865027	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs570888785	chr2:133865048-133865049	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs535095947	chr2:133865063-133865064	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs546748857	chr2:133865093-133865094	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs11887605	chr2:133865130-133865131	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs386650749	chr2:133865181-133865182	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs535611836	chr2:133865186-133865187	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs190421329	chr2:133865226-133865227	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs575529648	chr2:133865232-133865233	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs539088541	chr2:133865233-133865234	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs181686631	chr2:133865341-133865342	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs560537725	chr2:133865353-133865354	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs572882544	chr2:133865359-133865360	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs540346176	chr2:133865363-133865364	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs77932039	chr2:133865369-133865370	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs186797216	chr2:133865379-133865380	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs149020352	chr2:133865380-133865381	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs191584169	chr2:133865396-133865397	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs183938256	chr2:133865402-133865403	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs143829670	chr2:133865412-133865413	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs138458047	chr2:133865431-133865432	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs564526137	chr2:133865441-133865442	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs141366609	chr2:133865466-133865467	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs547080545	chr2:133865497-133865498	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs568168978	chr2:133865547-133865548	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs187812715	chr2:133865556-133865557	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs529491178	chr2:133865568-133865569	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs550753122	chr2:133865575-133865576	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs189653593	chr2:133865592-133865593	Weak transcription Enhancers	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:344 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:133853000-133867400	Weak transcription	Brain Hippocampus Middle	brain
2	chr2:133854600-133865000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr2:133854800-133892000	Weak transcription	Left Ventricle	heart
4	chr2:133855600-133867800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr2:133859600-133864800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr2:133864000-133864800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr2:133864000-133865800	Enhancers	Fetal Brain Male	brain
8	chr2:133865000-133867800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr2:133865200-133870400	Weak transcription	NHLF	lung
10	chr2:133866600-133868000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr2:133866600-133868400	Enhancers	NHDF-Ad	bronchial
12	chr2:133867200-133868000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr2:133867200-133868000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr2:133867200-133868400	Enhancers	NHEK	skin
15	chr2:133867400-133867800	Enhancers	HMEC	breast
16	chr2:133867400-133868000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr2:133867400-133868000	Enhancers	Brain Hippocampus Middle	brain
18	chr2:133867600-133868000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr2:133867600-133868400	Enhancers	Brain Substantia Nigra	brain
20	chr2:133867600-133868600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr2:133867800-133868200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr2:133867800-133868200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr2:133867800-133877000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr2:133868000-133870400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr2:133868000-133885200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr2:133868000-133888200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr2:133868200-133883600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr2:133870400-133870800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr2:133870400-133870800	Enhancers	NHLF	lung
30	chr2:133871200-133871400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr2:133871200-133871400	Enhancers	Pancreas	Pancrea
32	chr2:133871400-133876200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr2:133877000-133880400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr2:133877400-133879200	Enhancers	Stomach Mucosa	stomach
35	chr2:133877600-133878200	Enhancers	Cortex derived primary cultured neurospheres	brain
36	chr2:133878200-133887200	Weak transcription	Cortex derived primary cultured neurospheres	brain
37	chr2:133879800-133880800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr2:133880000-133880200	Enhancers	Brain Cingulate Gyrus	brain
39	chr2:133880000-133889200	Weak transcription	Liver	Liver
40	chr2:133880200-133880400	Enhancers	Brain Hippocampus Middle	brain
41	chr2:133880200-133880400	Enhancers	Ovary	ovary
42	chr2:133880200-133880600	Enhancers	Brain Substantia Nigra	brain
43	chr2:133880400-133880600	Enhancers	Brain Angular Gyrus	brain
44	chr2:133880400-133880600	Enhancers	Brain Anterior Caudate	brain
45	chr2:133880400-133881000	Weak transcription	Ovary	ovary
46	chr2:133880400-133888800	Weak transcription	Brain Hippocampus Middle	brain
47	chr2:133880400-133889000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr2:133880600-133881800	Weak transcription	Brain Anterior Caudate	brain
49	chr2:133880600-133896200	Weak transcription	Brain Substantia Nigra	brain
50	chr2:133880800-133886000	Weak transcription	Brain Angular Gyrus	brain

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