Variant report

Variant	nsv532651
Chromosome Location	chr2:50712339-50758351
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	chr2:50718755-50718994	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:50756786-50757088	HepG2	liver:	n/a	chr2:50757036-50757052 chr2:50757037-50757053
3	BHLHE40	chr2:50719650-50719971	GM12878	blood:	n/a	n/a
4	BHLHE40	chr2:50718813-50718826	K562	blood:	n/a	n/a
5	BRCA1	chr2:50719632-50719941	Hela-S3	cervix:	n/a	n/a
6	BRCA1	chr2:50756704-50757012	H1-hESC	embryonic stem cell:	n/a	n/a
7	CREB1	chr2:50742070-50742432	H1-hESC	embryonic stem cell:	n/a	n/a
8	CTCF	chr2:50718760-50718910	GM12866	blood:	n/a	chr2:50718868-50718889 chr2:50718866-50718884 chr2:50718869-50718882
9	CTCF	chr2:50718566-50720259	A549	lung:	n/a	chr2:50719790-50719811 chr2:50718868-50718889 chr2:50719800-50719808 chr2:50718866-50718884 chr2:50718869-50718882 chr2:50719796-50719812 chr2:50719795-50719813
10	CTCF	chr2:50718800-50718950	HPAF	blood vessel:	n/a	chr2:50718868-50718889 chr2:50718866-50718884 chr2:50718869-50718882
11	CTCF	chr2:50740969-50741132	H1-hESC	embryonic stem cell:	n/a	chr2:50741058-50741076 chr2:50741063-50741071 chr2:50741053-50741074 chr2:50741059-50741075
12	CTCF	chr2:50716300-50716450	HCT-116	colon:	n/a	n/a
13	CTCF	chr2:50719635-50719850	H1-hESC	embryonic stem cell:	n/a	chr2:50719790-50719811 chr2:50719800-50719808 chr2:50719796-50719812 chr2:50719795-50719813
14	CTCF	chr2:50718740-50718890	NHEK	skin:	n/a	chr2:50718868-50718889 chr2:50718866-50718884 chr2:50718869-50718882
15	CTCF	chr2:50718920-50719070	GM12865	blood:	n/a	n/a
16	CTCF	chr2:50718780-50718930	GM12801	blood:	n/a	chr2:50718868-50718889 chr2:50718866-50718884 chr2:50718869-50718882
17	CTCF	chr2:50756880-50757030	GM12874	blood:	n/a	chr2:50756940-50756958 chr2:50756945-50756953 chr2:50756942-50756963
18	CTCF	chr2:50756880-50757030	GM12871	blood:	n/a	chr2:50756940-50756958 chr2:50756945-50756953 chr2:50756942-50756963
19	CTCF	chr2:50718800-50718950	HL-60	blood:	n/a	chr2:50718868-50718889 chr2:50718866-50718884 chr2:50718869-50718882
20	CTCF	chr2:50756860-50757010	HCPEpiC	choroid plexus:	n/a	chr2:50756940-50756958 chr2:50756945-50756953 chr2:50756942-50756963
21	CTCF	chr2:50756760-50757063	GM12878	blood:	n/a	chr2:50756940-50756958 chr2:50756945-50756953 chr2:50756942-50756963
22	CTCF	chr2:50719501-50720081	HCT-116	colon:	n/a	chr2:50719790-50719811 chr2:50719800-50719808 chr2:50719796-50719812 chr2:50719795-50719813
23	CTCF	chr2:50756880-50757030	AG04450	lung:	n/a	chr2:50756940-50756958 chr2:50756945-50756953 chr2:50756942-50756963
24	CTCF	chr2:50720060-50720210	HPF	lung:	n/a	n/a
25	CTCF	chr2:50719700-50719850	GM12871	blood:	n/a	chr2:50719800-50719808 chr2:50719796-50719812 chr2:50719795-50719813 chr2:50719790-50719811
26	CTCF	chr2:50718760-50718910	GM12870	blood:	n/a	chr2:50718868-50718889 chr2:50718866-50718884 chr2:50718869-50718882
27	CTCF	chr2:50740960-50741110	HMEC	breast:	n/a	chr2:50741058-50741076 chr2:50741063-50741071 chr2:50741053-50741074 chr2:50741059-50741075
28	CTCF	chr2:50756780-50756930	GM12867	blood:	n/a	n/a
29	CTCF	chr2:50756766-50757072	SK-N-SH_RA	brain:	n/a	chr2:50756940-50756958 chr2:50756945-50756953 chr2:50756942-50756963
30	CTCF	chr2:50756800-50756950	GM12868	blood:	n/a	n/a
31	CTCF	chr2:50740980-50741130	HEEpiC	esophagus:	n/a	chr2:50741058-50741076 chr2:50741063-50741071 chr2:50741053-50741074 chr2:50741059-50741075
32	CTCF	chr2:50740960-50741110	AG04450	lung:	n/a	chr2:50741058-50741076 chr2:50741063-50741071 chr2:50741053-50741074 chr2:50741059-50741075
33	CTCF	chr2:50756789-50757148	HCT-116	colon:	n/a	chr2:50756940-50756958 chr2:50756945-50756953 chr2:50756942-50756963
34	CTCF	chr2:50740980-50741130	GM12873	blood:	n/a	chr2:50741058-50741076 chr2:50741063-50741071 chr2:50741053-50741074 chr2:50741059-50741075
35	CTCF	chr2:50719380-50719530	NHEK	skin:	n/a	n/a
36	CTCF	chr2:50719700-50719850	BE2_C	brain:	n/a	chr2:50719790-50719811 chr2:50719800-50719808 chr2:50719796-50719812 chr2:50719795-50719813
37	CTCF	chr2:50719700-50719850	HA-sp	spinal cord:	n/a	chr2:50719790-50719811 chr2:50719800-50719808 chr2:50719796-50719812 chr2:50719795-50719813
38	CTCF	chr2:50718880-50719030	NHDF-neo	bronchial:	n/a	n/a
39	CTCF	chr2:50756537-50757316	A549	lung:	n/a	chr2:50756940-50756958 chr2:50756945-50756953 chr2:50756942-50756963
40	CTCF	chr2:50756191-50756267	GM20000	blood:	n/a	n/a
41	CTCF	chr2:50718777-50718967	LNCaP	prostate:	n/a	chr2:50718868-50718889 chr2:50718866-50718884 chr2:50718869-50718882
42	CTCF	chr2:50718880-50719030	RPTEC	kidney:	n/a	n/a
43	CTCF	chr2:50740940-50741090	BE2_C	brain:	n/a	chr2:50741058-50741076 chr2:50741063-50741071 chr2:50741053-50741074 chr2:50741059-50741075
44	CTCF	chr2:50740940-50741090	Hela-S3	cervix:	n/a	chr2:50741058-50741076 chr2:50741063-50741071 chr2:50741053-50741074 chr2:50741059-50741075
45	CTCF	chr2:50719720-50719870	AG10803	skin:	n/a	chr2:50719790-50719811 chr2:50719800-50719808 chr2:50719796-50719812 chr2:50719795-50719813
46	CTCF	chr2:50756880-50757030	Hela-S3	cervix:	n/a	chr2:50756940-50756958 chr2:50756945-50756953 chr2:50756942-50756963
47	CTCF	chr2:50756880-50757030	NHDF-neo	bronchial:	n/a	chr2:50756940-50756958 chr2:50756945-50756953 chr2:50756942-50756963
48	CTCF	chr2:50719660-50719810	SAEC	small airway:	n/a	chr2:50719800-50719808
49	CTCF	chr2:50720140-50720290	NHLF	lung:	n/a	n/a
50	CTCF	chr2:50719099-50719143	GM10266	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:50718584-50718634	SK-N-SH	brain:	n/a
2	chr2:50718584-50718634	SK-N-SH	brain:	n/a
3	chr2:50718584-50718634	Hela-S3	cervix:	n/a
4	chr2:50718584-50718634	K562	blood:	n/a
5	chr2:50718584-50718634	HEK293	kidney:	embryo
6	chr2:50718584-50718634	HEEpiC	esophagus:	n/a
7	chr2:50718584-50718634	HCF	heart:	n/a
8	chr2:50718584-50718634	GM12878	blood:	n/a
9	chr2:50718584-50718634	ECC-1	luminal epithelium:	n/a
10	chr2:50718584-50718634	HIPEpiC	eye:	n/a
11	chr2:50718584-50718634	BE2_C	brain:	n/a
12	chr2:50718584-50718634	HMEC	breast:	n/a
13	chr2:50718584-50718634	NHBE	bronchial:	n/a
14	chr2:50718584-50718634	IMR90	lung:	fetal
15	chr2:50718584-50718634	H1-hESC	embryonic stem cell:	embryo
16	chr2:50718584-50718634	GM12891	blood:	n/a
17	chr2:50718584-50718634	AG09319	gingival:	n/a
18	chr2:50718584-50718634	MCF10A-Er-Src	breast:	n/a
19	chr2:50718584-50718634	CMK	blood:	n/a
20	chr2:50718584-50718634	AG04450	lung:	fetal
21	chr2:50718584-50718634	MCF-7	breast:	n/a
22	chr2:50718584-50718634	SAEC	small airway:	n/a
23	chr2:50718584-50718634	ovcar-3	ovarian:	n/a
24	chr2:50718584-50718634	HCPEpiC	choroid plexus:	n/a
25	chr2:50718584-50718634	PANC-1	pancreas:	n/a
26	chr2:50718584-50718634	HPAEpiC	pulmonary alveolar:	n/a
27	chr2:50718584-50718634	HCM	heart:	n/a
28	chr2:50718584-50718634	SK-N-MC	brain:	n/a
29	chr2:50718584-50718634	HCT-116	colon:	n/a
30	chr2:50718584-50718634	GM12892	blood:	n/a
31	chr2:50718584-50718634	NB4	blood:	n/a
32	chr2:50718584-50718634	BJ	skin:	n/a
33	chr2:50718584-50718634	SKMC	muscle:	n/a
34	chr2:50718584-50718634	HAEpiC	amniotic membrane:	n/a
35	chr2:50718584-50718634	Hepatocyte	liver:	n/a
36	chr2:50718584-50718634	AoSMC	blood vessel:	n/a
37	chr2:50718584-50718634	HRPEpiC	eye:	n/a
38	chr2:50718584-50718634	ProgFib	skin:	n/a
39	chr2:50718584-50718634	PrEC	prostate:	n/a
40	chr2:50718584-50718634	HNPCEpiC	eye:	n/a
41	chr2:50718584-50718634	RPTEC	kidney:	n/a
42	chr2:50718584-50718634	AG09309	skin:	n/a
43	chr2:50718584-50718634	AG10803	skin:	n/a
44	chr2:50718584-50718634	HL-60	blood:	n/a
45	chr2:50718584-50718634	HRCEpiC	kidney:	n/a
46	chr2:50718584-50718634	NHDF-neo	bronchial:	n/a
47	chr2:50718584-50718634	Jurkat	blood:	n/a
48	chr2:50718584-50718634	AG04449	skin:	fetal
49	chr2:50718584-50718634	NT2-D1	testis:	n/a
50	chr2:50718584-50718634	HRE	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:48772065..48772805-chr2:50719351..50720113,2	K562	blood:
2	chr2:50756714..50757394-chr2:52022672..52023233,2	MCF-7	breast:
3	chr2:50748617..50751233-chr2:50751871..50754542,2	K562	blood:
4	chr2:50629632..50630141-chr2:50719329..50719849,2	MCF-7	breast:
5	chr2:50712217..50714362-chr2:50715383..50718092,2	MCF-7	breast:
6	chr2:50712217..50714362-chr2:50715383..50718092,2	MCF-7	breast:
7	chr2:50551521..50552446-chr2:50719322..50720205,2	MCF-7	breast:
8	chr2:50571653..50572272-chr2:50719383..50719965,2	MCF-7	breast:
9	chr2:50748617..50751233-chr2:50751871..50754542,2	K562	blood:

Variant related genes	Relation type
NRXN1	TF binding region
NRXN1	CpG island

Extended variants
information (count: 2239 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:2239 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs574041767	chr2:50712374-50712375	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs191065617	chr2:50712404-50712405	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs556553050	chr2:50712407-50712408	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs541991508	chr2:50712493-50712494	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs561825323	chr2:50712525-50712526	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs80304543	chr2:50712551-50712552	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs545683108	chr2:50712592-50712593	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs560752156	chr2:50712612-50712613	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs200271042	chr2:50712651-50712652	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs542848886	chr2:50712652-50712653	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs368064750	chr2:50712657-50712658	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs182038061	chr2:50712667-50712668	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs549369363	chr2:50712678-50712679	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs186909630	chr2:50712694-50712695	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs532286416	chr2:50712695-50712696	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs370481728	chr2:50712700-50712701	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs544360383	chr2:50712746-50712747	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs115290734	chr2:50712748-50712749	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs190405830	chr2:50712771-50712772	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs536489540	chr2:50712845-50712846	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs548042803	chr2:50712866-50712867	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs567754307	chr2:50712868-50712869	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs538317765	chr2:50712883-50712884	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs371993119	chr2:50712888-50712889	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs183438479	chr2:50712889-50712890	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs578095747	chr2:50712896-50712897	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs539013186	chr2:50712897-50712898	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs375618712	chr2:50712941-50712942	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs564444082	chr2:50712952-50712953	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs533503323	chr2:50712968-50712969	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs112871033	chr2:50712981-50712982	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs6721498	chr2:50713012-50713013	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs112448128	chr2:50713042-50713043	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs565575515	chr2:50713091-50713092	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs117699010	chr2:50713113-50713114	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs576106882	chr2:50713120-50713121	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs13423536	chr2:50713147-50713148	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs533066286	chr2:50713219-50713220	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs80055048	chr2:50713222-50713223	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs147725631	chr2:50713242-50713243	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs546982324	chr2:50713288-50713289	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs79150744	chr2:50713315-50713316	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs6724631	chr2:50713331-50713332	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs6739559	chr2:50713367-50713368	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs568125609	chr2:50713399-50713400	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs111585620	chr2:50713408-50713409	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs13423870	chr2:50713410-50713411	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs377308832	chr2:50713428-50713429	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs13410477	chr2:50713448-50713449	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs76698602	chr2:50713457-50713458	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
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
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	16272173	CNVD
Lung cancer	17297452	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	20433910	CNVD
Autism	21701786	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Austim spectrum disorder	21302340	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	20553308	CNVD
Autism	22241247	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Retinoblastoma	22278416	CNVD
Cancer	21183584	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	18768390	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	18940311	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18945720	CNVD
Schizophrenia	19571808	CNVD
Prostate cancer	16573809	CNVD
Neuroticism	17667963	CNVD
Schizophrenia	19443537	CNVD
Schizophrenia	19546859	CNVD
Autism	17322880	CNVD
Lung cancer	17086460	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Hereditary non-polyposis colorectal cancer	19566914	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Basal cell lymphoma	21115979	CNVD
Cognitive impairment	21505072	CNVD
Psychiatric disorder	19734545	CNVD
Autism	20844286	CNVD
Schizophrenia	20838587	CNVD
Schizophrenia	20718829	CNVD
Autism	19218893	CNVD
Autism	22209245	CNVD
Neuropsychiatric disorder	21827697	CNVD
Schizophrenia	22118685	CNVD
Autism	20663923	CNVD
Schizophrenia	21285140	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21990379	CNVD
Schizophrenia	22885689	CNVD
Autism	20964600	CNVD
Schizophrenia	19521646	CNVD
Attention deficit hyperactivity disorder	22214315	CNVD
Chronic motor tic disorder	22214315	CNVD
Schizophrenia	22214315	CNVD
Mental retardation	19896112	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute myeloid leukemia	20729466	CNVD

Chromatin state (count:215 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:50691200-50716000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr2:50691600-50718600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr2:50699000-50742000	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr2:50704400-50718600	Weak transcription	Fetal Brain Male	brain
5	chr2:50706200-50719000	Weak transcription	Stomach Mucosa	stomach
6	chr2:50706600-50719400	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr2:50710000-50712400	Weak transcription	Brain Germinal Matrix	brain
8	chr2:50711600-50716600	Strong transcription	Fetal Brain Female	brain
9	chr2:50712400-50714600	Strong transcription	Brain Germinal Matrix	brain
10	chr2:50712600-50718800	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr2:50713400-50718200	Weak transcription	Brain Angular Gyrus	brain
12	chr2:50714600-50715800	Weak transcription	Brain Germinal Matrix	brain
13	chr2:50714600-50718600	Weak transcription	Brain Anterior Caudate	brain
14	chr2:50715800-50716200	Strong transcription	Brain Germinal Matrix	brain
15	chr2:50716000-50716200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr2:50716000-50716200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
17	chr2:50716000-50716400	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr2:50716000-50717800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr2:50716200-50717000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr2:50716200-50718600	Weak transcription	Brain Germinal Matrix	brain
21	chr2:50716400-50717400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
22	chr2:50716400-50719200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr2:50716600-50719000	Weak transcription	Fetal Brain Female	brain
24	chr2:50717000-50717400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr2:50717200-50717400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr2:50717400-50717600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr2:50717400-50718400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
28	chr2:50717400-50719400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr2:50717600-50719000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr2:50717600-50719200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr2:50717600-50719200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr2:50717800-50718400	Enhancers	Primary hematopoietic stem cells	blood
33	chr2:50717800-50719200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr2:50717800-50719400	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr2:50717800-50719600	Enhancers	Primary hematopoietic stem cells short term culture	blood
36	chr2:50717800-50724000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr2:50718200-50718400	Enhancers	Brain Angular Gyrus	brain
38	chr2:50718200-50719200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr2:50718200-50719600	Enhancers	NHEK	skin
40	chr2:50718200-50719800	Enhancers	HMEC	breast
41	chr2:50718400-50718800	Weak transcription	Primary hematopoietic stem cells	blood
42	chr2:50718400-50719200	Weak transcription	Brain Angular Gyrus	brain
43	chr2:50718400-50719200	Enhancers	Brain Hippocampus Middle	brain
44	chr2:50718400-50719400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
45	chr2:50718400-50719800	Enhancers	Primary T helper cells fromperipheralblood	blood
46	chr2:50718600-50719200	Enhancers	Brain Anterior Caudate	brain
47	chr2:50718600-50719200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
48	chr2:50718600-50719400	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr2:50718600-50719600	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr2:50718600-50719600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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