Variant report

Variant	nsv520225
Chromosome Location	chr2:50983186-51082754
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	chr2:51077746-51078099	IMR90	lung:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
2	CEBPB	chr2:51077727-51078088	H1-hESC	embryonic stem cell:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
3	CEBPB	chr2:51042082-51042350	A549	lung:	n/a	chr2:51042175-51042186
4	CEBPB	chr2:51077720-51078095	HepG2	liver:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
5	CEBPB	chr2:51080929-51081152	A549	lung:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
6	CEBPB	chr2:51042035-51042364	HepG2	liver:	n/a	chr2:51042175-51042186
7	CEBPB	chr2:51077732-51078049	Hela-S3	cervix:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
8	CEBPB	chr2:51039958-51040191	HepG2	liver:	n/a	n/a
9	CEBPB	chr2:51080882-51081169	HepG2	liver:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
10	CEBPB	chr2:51003545-51003679	IMR90	lung:	n/a	n/a
11	CEBPB	chr2:51080924-51081178	H1-hESC	embryonic stem cell:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
12	CEBPB	chr2:51068879-51068992	HepG2	liver:	n/a	chr2:51068958-51068969
13	CEBPB	chr2:51080873-51081218	IMR90	lung:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
14	CEBPB	chr2:51077765-51078077	A549	lung:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
15	CEBPB	chr2:51051532-51051664	HepG2	liver:	n/a	chr2:51051618-51051629 chr2:51051616-51051627 chr2:51051616-51051629
16	CEBPB	chr2:51080893-51081164	Hela-S3	cervix:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
17	CHD2	chr2:51020103-51020131	GM12878	blood:	n/a	n/a
18	CTCF	chr2:51013610-51013718	HUVEC	blood vessel:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
19	CTCF	chr2:51013640-51013790	RPTEC	kidney:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
20	CTCF	chr2:51075262-51075348	Kidney_OC	kidney:	n/a	n/a
21	CTCF	chr2:51013660-51013810	RPTEC	kidney:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
22	CTCF	chr2:51013623-51013763	Hela-S3	cervix:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
23	CTCF	chr2:51013560-51013710	HBMEC	blood vessel:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
24	CTCF	chr2:51040238-51040274	A549	lung:	n/a	n/a
25	CTCF	chr2:51013620-51013770	WERI-Rb-1	eye:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
26	CTCF	chr2:51009720-51009870	AG04450	lung:	n/a	chr2:51009841-51009854
27	CTCF	chr2:51013620-51013770	HCT-116	colon:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
28	CTCF	chr2:51015540-51015690	HCT-116	colon:	n/a	n/a
29	CTCF	chr2:51013600-51013750	HEK293	kidney:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
30	CTCF	chr2:51040080-51040230	GM12874	blood:	n/a	n/a
31	CTCF	chr2:51009680-51009830	HRE	kidney:	n/a	n/a
32	CTCF	chr2:51013660-51013810	GM12873	blood:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
33	CTCF	chr2:51013600-51013750	NHEK	skin:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
34	CTCF	chr2:51056731-51056889	GM20000	blood:	n/a	n/a
35	CTCF	chr2:51013580-51013730	HRE	kidney:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
36	CTCF	chr2:51013620-51013770	SK-N-SH_RA	brain:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
37	CTCF	chr2:51013580-51013730	AG04450	lung:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
38	CTCF	chr2:51013600-51013750	BE2_C	brain:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
39	CTCF	chr2:51009804-51009856	Hela-S3	cervix:	n/a	chr2:51009841-51009854
40	CTCF	chr2:51013640-51013790	AG04450	lung:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
41	CTCF	chr2:51013607-51013764	Kidney_OC	kidney:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
42	CTCF	chr2:51009780-51009930	Caco-2	colon:	n/a	chr2:51009841-51009854
43	CTCF	chr2:51013540-51013690	GM12866	blood:	n/a	n/a
44	CTCF	chr2:51013580-51013730	WERI-Rb-1	eye:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
45	CTCF	chr2:51009760-51009910	HBMEC	blood vessel:	n/a	chr2:51009841-51009854
46	CTCF	chr2:51009820-51009970	AG04450	lung:	n/a	chr2:51009841-51009854
47	CTCF	chr2:51013578-51013819	Medullo	brain:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
48	CTCF	chr2:51013580-51013730	HRPEpiC	eye:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
49	CTCF	chr2:51013540-51013690	HCT-116	colon:	n/a	n/a
50	CTCF	chr2:51013675-51013707	K562	blood:	n/a	chr2:51013679-51013695 chr2:51013678-51013696

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:51065673-51065723	HEK293	kidney:	embryo
2	chr2:51065673-51065723	HEK293	kidney:	embryo
3	chr2:51056822-51056872	AG10803	skin:	n/a
4	chr2:51001003-51001053	ProgFib	skin:	n/a
5	chr2:51056884-51056934	PFSK-1	brain:	n/a
6	chr2:51001003-51001053	NHBE	bronchial:	n/a
7	chr2:51056884-51056934	H1-hESC	embryonic stem cell:	embryo
8	chr2:51057218-51057268	HL-60	blood:	n/a
9	chr2:50992829-50992879	HCM	heart:	n/a
10	chr2:51056884-51056934	MCF10A-Er-Src	breast:	n/a
11	chr2:51074881-51074931	NH-A	brain:	n/a
12	chr2:51065673-51065723	MCF-7	breast:	n/a
13	chr2:51001003-51001053	Jurkat	blood:	n/a
14	chr2:50992829-50992879	GM06990	blood:	n/a
15	chr2:51056884-51056934	SKMC	muscle:	n/a
16	chr2:51057548-51057598	NH-A	brain:	n/a
17	chr2:51074881-51074931	AoSMC	blood vessel:	n/a
18	chr2:51074939-51074989	Jurkat	blood:	n/a
19	chr2:51074881-51074931	PrEC	prostate:	n/a
20	chr2:51057218-51057268	HMEC	breast:	n/a
21	chr2:51057548-51057598	SK-N-SH	brain:	n/a
22	chr2:50992829-50992879	HNPCEpiC	eye:	n/a
23	chr2:50992829-50992879	NHBE	bronchial:	n/a
24	chr2:51074939-51074989	NHDF-neo	bronchial:	n/a
25	chr2:51074881-51074931	HCF	heart:	n/a
26	chr2:51074939-51074989	HRE	kidney:	n/a
27	chr2:51001003-51001053	CMK	blood:	n/a
28	chr2:51074939-51074989	IMR90	lung:	fetal
29	chr2:51056884-51056934	AG09309	skin:	n/a
30	chr2:51001003-51001053	Hela-S3	cervix:	n/a
31	chr2:50992829-50992879	ProgFib	skin:	n/a
32	chr2:50992829-50992879	GM12878	blood:	n/a
33	chr2:51074881-51074931	ECC-1	luminal epithelium:	n/a
34	chr2:50992829-50992879	PFSK-1	brain:	n/a
35	chr2:51074881-51074931	AG09319	gingival:	n/a
36	chr2:50992829-50992879	PrEC	prostate:	n/a
37	chr2:51074881-51074931	NB4	blood:	n/a
38	chr2:51001003-51001053	HRPEpiC	eye:	n/a
39	chr2:51074939-51074989	AoSMC	blood vessel:	n/a
40	chr2:51056822-51056872	AG04449	skin:	fetal
41	chr2:50992829-50992879	SK-N-MC	brain:	n/a
42	chr2:51074939-51074989	HEEpiC	esophagus:	n/a
43	chr2:51056822-51056872	AG09309	skin:	n/a
44	chr2:51057548-51057598	AG10803	skin:	n/a
45	chr2:51001003-51001053	H1-hESC	embryonic stem cell:	embryo
46	chr2:51074881-51074931	HRPEpiC	eye:	n/a
47	chr2:51056884-51056934	HCM	heart:	n/a
48	chr2:51001003-51001053	BJ	skin:	n/a
49	chr2:51001003-51001053	GM12892	blood:	n/a
50	chr2:51057548-51057598	PrEC	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:51018306..51019906-chr2:51022210..51025087,2	K562	blood:
2	chr2:50985182..50988156-chr2:50995412..50998213,2	K562	blood:
3	chr2:51018306..51019906-chr2:51022210..51025087,2	K562	blood:
4	chr2:50985182..50988156-chr2:50995412..50998213,2	K562	blood:
5	chr2:50977335..50979735-chr2:50992909..50995322,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FSHR-5	chr2:51056580-51056816	NONHSAT070648

Variant related genes	Relation type
ENSG00000238165	TF binding region
ENSG00000215968	TF binding region
ENSG00000238165	CpG island
ENSG00000215968	CpG island

Extended variants
information (count: 3618 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:3618 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17041014	chr2:50983186-50983187	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs141194832	chr2:50983188-50983189	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs373722055	chr2:50983201-50983202	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs565585636	chr2:50983210-50983211	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs535932790	chr2:50983248-50983249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs143306139	chr2:50983262-50983263	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs540398531	chr2:50983264-50983265	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs560620589	chr2:50983278-50983279	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs185945325	chr2:50983280-50983281	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs148316078	chr2:50983341-50983342	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs549138338	chr2:50983342-50983343	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs562846086	chr2:50983362-50983363	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs141533258	chr2:50983381-50983382	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs578201408	chr2:50983395-50983396	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs545025370	chr2:50983427-50983428	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs560532211	chr2:50983435-50983436	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs572510467	chr2:50983457-50983458	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs72889405	chr2:50983550-50983551	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs561391384	chr2:50983592-50983593	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs531500786	chr2:50983645-50983646	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs549959079	chr2:50983712-50983713	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs190119495	chr2:50983721-50983722	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs532433933	chr2:50983818-50983819	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs547415219	chr2:50983832-50983833	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs150443266	chr2:50983867-50983868	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs9309193	chr2:50983957-50983958	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs547852575	chr2:50984006-50984007	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs569426054	chr2:50984051-50984052	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs538006926	chr2:50984052-50984053	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs181072901	chr2:50984086-50984087	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs77914523	chr2:50984160-50984161	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs539306261	chr2:50984161-50984162	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs185946913	chr2:50984191-50984192	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs190604170	chr2:50984215-50984216	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs183356862	chr2:50984239-50984240	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs78691803	chr2:50984252-50984253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs546391374	chr2:50984273-50984274	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs576615720	chr2:50984283-50984284	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs116777909	chr2:50984322-50984323	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs565080580	chr2:50984332-50984333	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs566531025	chr2:50984354-50984355	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs532240747	chr2:50984444-50984445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs111776983	chr2:50984471-50984472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs547646039	chr2:50984501-50984502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs372182571	chr2:50984537-50984538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs189210345	chr2:50984559-50984560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs529605665	chr2:50984612-50984613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs547790343	chr2:50984632-50984633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs569361794	chr2:50984669-50984670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs144141400	chr2:50984696-50984697	Weak 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
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
Schizophrenia	20967226	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:359 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:50976600-50983200	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr2:50977400-50983600	Weak transcription	Brain Hippocampus Middle	brain
3	chr2:50977400-50984400	Enhancers	Fetal Brain Female	brain
4	chr2:50978400-50984400	Enhancers	Fetal Brain Male	brain
5	chr2:50980800-50984000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr2:50981200-50983400	Enhancers	Pancreatic Islets	Pancreatic Islet
7	chr2:50982000-50983200	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr2:50982600-50983400	Weak transcription	Brain Germinal Matrix	brain
9	chr2:50982600-50991200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr2:50983000-50983200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr2:50983000-50983600	Weak transcription	Brain Substantia Nigra	brain
12	chr2:50983200-50983400	Enhancers	Brain Inferior Temporal Lobe	brain
13	chr2:50983200-50983600	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr2:50983200-50991800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr2:50983200-50996800	Weak transcription	Cortex derived primary cultured neurospheres	brain
16	chr2:50983400-50983600	Enhancers	Brain Germinal Matrix	brain
17	chr2:50983400-50983800	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr2:50983600-50983800	Enhancers	Brain Hippocampus Middle	brain
19	chr2:50983600-50983800	Enhancers	Brain Substantia Nigra	brain
20	chr2:50983800-50984200	Enhancers	Brain Inferior Temporal Lobe	brain
21	chr2:50984000-50984400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr2:50990800-50991200	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr2:50991200-50991800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr2:50991200-50992200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr2:50991200-50992600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr2:50991400-50993400	Enhancers	Pancreatic Islets	Pancreatic Islet
27	chr2:50991800-50993000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr2:50991800-50993400	Enhancers	Brain Cingulate Gyrus	brain
29	chr2:50991800-50997000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr2:50992000-50993000	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr2:50992000-50993000	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr2:50992200-50992800	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr2:50992200-50992800	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr2:50992200-50993400	Enhancers	Fetal Kidney	kidney
35	chr2:50992400-50992600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr2:50992400-50993000	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr2:50992600-50992800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr2:50992600-50993000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr2:50992800-50993600	Enhancers	Brain Anterior Caudate	brain
40	chr2:50992800-50994200	Weak transcription	HUES48 Cell Line	embryonic stem cell
41	chr2:50992800-51000800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr2:50993000-50994000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr2:50993000-50994400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
44	chr2:50993000-50998800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr2:50993000-50999200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
46	chr2:50993000-51000800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
47	chr2:50993400-50995600	Weak transcription	Pancreatic Islets	Pancreatic Islet
48	chr2:50993400-50996000	Weak transcription	Brain Cingulate Gyrus	brain
49	chr2:50993600-50994200	Enhancers	Brain Germinal Matrix	brain
50	chr2:50993600-50996800	Weak transcription	Brain Anterior Caudate	brain

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