Variant report

Variant	nsv581850
Chromosome Location	chr2:50992027-51129285
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	BACH1	chr2:51083034-51083154	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr2:51080924-51081178	H1-hESC	embryonic stem cell:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
3	CEBPB	chr2:51077727-51078088	H1-hESC	embryonic stem cell:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
4	CEBPB	chr2:51127917-51128117	HepG2	liver:	n/a	n/a
5	CEBPB	chr2:51068879-51068992	HepG2	liver:	n/a	chr2:51068958-51068969
6	CEBPB	chr2:51042035-51042364	HepG2	liver:	n/a	chr2:51042175-51042186
7	CEBPB	chr2:51084911-51085196	IMR90	lung:	n/a	chr2:51085060-51085071
8	CEBPB	chr2:51084914-51085194	A549	lung:	n/a	chr2:51085060-51085071
9	CEBPB	chr2:51051532-51051664	HepG2	liver:	n/a	chr2:51051618-51051629 chr2:51051616-51051627 chr2:51051616-51051629
10	CEBPB	chr2:51080893-51081164	Hela-S3	cervix:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
11	CEBPB	chr2:51039958-51040191	HepG2	liver:	n/a	n/a
12	CEBPB	chr2:51077720-51078095	HepG2	liver:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
13	CEBPB	chr2:51077732-51078049	Hela-S3	cervix:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
14	CEBPB	chr2:51003545-51003679	IMR90	lung:	n/a	n/a
15	CEBPB	chr2:51042082-51042350	A549	lung:	n/a	chr2:51042175-51042186
16	CEBPB	chr2:51084918-51085221	HepG2	liver:	n/a	chr2:51085060-51085071
17	CEBPB	chr2:51084920-51085210	H1-hESC	embryonic stem cell:	n/a	chr2:51085060-51085071
18	CEBPB	chr2:51077765-51078077	A549	lung:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
19	CEBPB	chr2:51080882-51081169	HepG2	liver:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
20	CEBPB	chr2:51077746-51078099	IMR90	lung:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
21	CEBPB	chr2:51106584-51106784	HepG2	liver:	n/a	n/a
22	CEBPB	chr2:51080929-51081152	A549	lung:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
23	CEBPB	chr2:51080873-51081218	IMR90	lung:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
24	CHD2	chr2:51020103-51020131	GM12878	blood:	n/a	n/a
25	CTCF	chr2:51086360-51086510	WERI-Rb-1	eye:	n/a	n/a
26	CTCF	chr2:51013540-51013690	HCT-116	colon:	n/a	n/a
27	CTCF	chr2:51099780-51099930	HRPEpiC	eye:	n/a	n/a
28	CTCF	chr2:51099780-51099930	HMEC	breast:	n/a	n/a
29	CTCF	chr2:51009720-51009870	AG04450	lung:	n/a	chr2:51009841-51009854
30	CTCF	chr2:51099780-51099930	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr2:51013600-51013750	NHEK	skin:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
32	CTCF	chr2:51099800-51099950	AG04450	lung:	n/a	n/a
33	CTCF	chr2:51013578-51013819	Medullo	brain:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
34	CTCF	chr2:51099780-51099930	Caco-2	colon:	n/a	n/a
35	CTCF	chr2:51099740-51099890	HCT-116	colon:	n/a	n/a
36	CTCF	chr2:51099800-51099950	Caco-2	colon:	n/a	n/a
37	CTCF	chr2:51099940-51100090	NHEK	skin:	n/a	n/a
38	CTCF	chr2:51099800-51099901	NHEK	skin:	n/a	n/a
39	CTCF	chr2:51099757-51100003	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr2:51099880-51100030	HCT-116	colon:	n/a	n/a
41	CTCF	chr2:51086260-51086410	BE2_C	brain:	n/a	n/a
42	CTCF	chr2:51013675-51013707	K562	blood:	n/a	chr2:51013679-51013695 chr2:51013678-51013696
43	CTCF	chr2:51009804-51009856	Hela-S3	cervix:	n/a	chr2:51009841-51009854
44	CTCF	chr2:51009760-51009910	HBMEC	blood vessel:	n/a	chr2:51009841-51009854
45	CTCF	chr2:51015540-51015690	HCT-116	colon:	n/a	n/a
46	CTCF	chr2:51056731-51056889	GM20000	blood:	n/a	n/a
47	CTCF	chr2:51009780-51009930	Caco-2	colon:	n/a	chr2:51009841-51009854
48	CTCF	chr2:51099740-51099890	RPTEC	kidney:	n/a	n/a
49	CTCF	chr2:51009680-51009830	HRE	kidney:	n/a	n/a
50	CTCF	chr2:51013640-51013790	HRPEpiC	eye:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:51056822-51056872	MCF-7	breast:	n/a
2	chr2:51074939-51074989	GM12891	blood:	n/a
3	chr2:51057218-51057268	MCF10A-Er-Src	breast:	n/a
4	chr2:51056822-51056872	SK-N-SH_RA	brain:	n/a
5	chr2:51057548-51057598	HL-60	blood:	n/a
6	chr2:51057218-51057268	AG10803	skin:	n/a
7	chr2:51065673-51065723	AG09319	gingival:	n/a
8	chr2:51074939-51074989	HEEpiC	esophagus:	n/a
9	chr2:51056822-51056872	A549	lung:	n/a
10	chr2:51074881-51074931	HIPEpiC	eye:	n/a
11	chr2:50992829-50992879	HAEpiC	amniotic membrane:	n/a
12	chr2:50992829-50992879	GM19239	blood:	n/a
13	chr2:51074939-51074989	SK-N-MC	brain:	n/a
14	chr2:51001003-51001053	HepG2	liver:	n/a
15	chr2:51001003-51001053	GM06990	blood:	n/a
16	chr2:51065673-51065723	U87	brain:	n/a
17	chr2:51056822-51056872	BE2_C	brain:	n/a
18	chr2:51057218-51057268	HMEC	breast:	n/a
19	chr2:51065673-51065723	A549	lung:	n/a
20	chr2:50992829-50992879	HUVEC	blood vessel:	n/a
21	chr2:51057218-51057268	AG09309	skin:	n/a
22	chr2:51001003-51001053	NHBE	bronchial:	n/a
23	chr2:51056822-51056872	HCT-116	colon:	n/a
24	chr2:50992829-50992879	HCT-116	colon:	n/a
25	chr2:50992829-50992879	K562	blood:	n/a
26	chr2:51057548-51057598	NHDF-neo	bronchial:	n/a
27	chr2:51056884-51056934	LNCaP	prostate:	n/a
28	chr2:51074939-51074989	U87	brain:	n/a
29	chr2:51057218-51057268	A549	lung:	n/a
30	chr2:50992829-50992879	HRCEpiC	kidney:	n/a
31	chr2:50992829-50992879	HCF	heart:	n/a
32	chr2:51057548-51057598	Jurkat	blood:	n/a
33	chr2:51065673-51065723	MCF10A-Er-Src	breast:	n/a
34	chr2:51001003-51001053	U87	brain:	n/a
35	chr2:51001003-51001053	Caco-2	colon:	n/a
36	chr2:51074939-51074989	HNPCEpiC	eye:	n/a
37	chr2:51065673-51065723	K562	blood:	n/a
38	chr2:51074939-51074989	AG09319	gingival:	n/a
39	chr2:51056822-51056872	AG04450	lung:	fetal
40	chr2:50992829-50992879	PFSK-1	brain:	n/a
41	chr2:51056884-51056934	T-47D	breast:	n/a
42	chr2:51074939-51074989	AG10803	skin:	n/a
43	chr2:51074939-51074989	HUVEC	blood vessel:	n/a
44	chr2:51074939-51074989	SK-N-SH	brain:	n/a
45	chr2:51057548-51057598	AG10803	skin:	n/a
46	chr2:51001003-51001053	IMR90	lung:	fetal
47	chr2:51074881-51074931	HRPEpiC	eye:	n/a
48	chr2:51074939-51074989	Caco-2	colon:	n/a
49	chr2:51056822-51056872	NHDF-neo	bronchial:	n/a
50	chr2:51057218-51057268	HNPCEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:51084150..51086897-chr2:51088805..51090362,2	K562	blood:
2	chr2:51084150..51086897-chr2:51088805..51090362,2	K562	blood:
3	chr2:51018306..51019906-chr2:51022210..51025087,2	K562	blood:
4	chr2:51113708..51115897-chr2:51117205..51120148,2	K562	blood:
5	chr2:51107834..51110098-chr2:51577616..51579275,2	K562	blood:
6	chr2:51113708..51115897-chr2:51117205..51120148,2	K562	blood:
7	chr2:50985182..50988156-chr2:50995412..50998213,2	K562	blood:
8	chr2:51018306..51019906-chr2:51022210..51025087,2	K562	blood:
9	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: 4791 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:4791 , 50 per page) page: 1 2 3 4 5 6 7 ... 96

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9309195	chr2:50992027-50992028	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs145479318	chr2:50992043-50992044	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs373497095	chr2:50992057-50992058	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs9309196	chr2:50992109-50992110	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs557795455	chr2:50992111-50992112	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs562575205	chr2:50992116-50992117	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs371155879	chr2:50992128-50992129	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs374886582	chr2:50992135-50992136	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs377321895	chr2:50992153-50992154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs558653441	chr2:50992164-50992165	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs556655929	chr2:50992196-50992197	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs576600544	chr2:50992197-50992198	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs531396827	chr2:50992223-50992224	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs534521740	chr2:50992244-50992245	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs191461396	chr2:50992295-50992296	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs574393443	chr2:50992296-50992297	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs370804015	chr2:50992307-50992308	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs182853678	chr2:50992313-50992314	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs575224439	chr2:50992345-50992346	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs545553105	chr2:50992348-50992349	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs147689502	chr2:50992351-50992352	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs571468346	chr2:50992428-50992429	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs532714957	chr2:50992439-50992440	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs188175968	chr2:50992521-50992522	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs142553629	chr2:50992530-50992531	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs192968588	chr2:50992559-50992560	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs548895866	chr2:50992588-50992589	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs182853375	chr2:50992629-50992630	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs10176529	chr2:50992650-50992651	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs552218762	chr2:50992663-50992664	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs368470641	chr2:50992776-50992777	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs187933007	chr2:50992778-50992779	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs76159848	chr2:50992829-50992830	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs552744622	chr2:50992830-50992831	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs114290796	chr2:50992882-50992883	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs3914723	chr2:50992927-50992928	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs549722481	chr2:50992962-50992963	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs529303444	chr2:50992969-50992970	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs575097233	chr2:50993011-50993012	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs192302900	chr2:50993014-50993015	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs3914724	chr2:50993048-50993049	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs183639819	chr2:50993061-50993062	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs146710943	chr2:50993064-50993065	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs559969100	chr2:50993084-50993085	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs116280866	chr2:50993100-50993101	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs542126701	chr2:50993104-50993105	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs564022177	chr2:50993168-50993169	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs530771900	chr2:50993199-50993200	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs539167776	chr2:50993326-50993327	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs552155514	chr2:50993387-50993388	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:107)

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
Schizophrenia	17989066	CNVD
Autism	19404257	CNVD

Chromatin state (count:412 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:50983200-50996800	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr2:50991200-50992200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr2:50991200-50992600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr2:50991400-50993400	Enhancers	Pancreatic Islets	Pancreatic Islet
5	chr2:50991800-50993000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr2:50991800-50993400	Enhancers	Brain Cingulate Gyrus	brain
7	chr2:50991800-50997000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr2:50992000-50993000	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr2:50992000-50993000	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr2:50992200-50992800	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr2:50992200-50992800	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr2:50992200-50993400	Enhancers	Fetal Kidney	kidney
13	chr2:50992400-50992600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr2:50992400-50993000	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr2:50992600-50992800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr2:50992600-50993000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr2:50992800-50993600	Enhancers	Brain Anterior Caudate	brain
18	chr2:50992800-50994200	Weak transcription	HUES48 Cell Line	embryonic stem cell
19	chr2:50992800-51000800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr2:50993000-50994000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr2:50993000-50994400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
22	chr2:50993000-50998800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr2:50993000-50999200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
24	chr2:50993000-51000800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr2:50993400-50995600	Weak transcription	Pancreatic Islets	Pancreatic Islet
26	chr2:50993400-50996000	Weak transcription	Brain Cingulate Gyrus	brain
27	chr2:50993600-50994200	Enhancers	Brain Germinal Matrix	brain
28	chr2:50993600-50996800	Weak transcription	Brain Anterior Caudate	brain
29	chr2:50994000-50996200	Weak transcription	Fetal Brain Female	brain
30	chr2:50994000-50996600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr2:50994200-50994800	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr2:50994400-50995000	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr2:50994800-50999800	Weak transcription	HUES48 Cell Line	embryonic stem cell
34	chr2:50995000-51000600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
35	chr2:50995600-50996200	Enhancers	Pancreatic Islets	Pancreatic Islet
36	chr2:50995800-50997400	Enhancers	Fetal Brain Male	brain
37	chr2:50996000-50996400	Enhancers	Brain Cingulate Gyrus	brain
38	chr2:50996000-50997200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr2:50996000-50997400	Enhancers	Duodenum Mucosa	Duodenum
40	chr2:50996200-50996600	Enhancers	Fetal Intestine Small	intestine
41	chr2:50996200-50996600	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
42	chr2:50996200-50996800	Enhancers	Fetal Brain Female	brain
43	chr2:50996400-50997200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr2:50996400-50997200	Enhancers	Fetal Intestine Large	intestine
45	chr2:50996400-51000800	Weak transcription	Brain Cingulate Gyrus	brain
46	chr2:50996600-50997000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr2:50996600-50997000	Weak transcription	Fetal Intestine Small	intestine
48	chr2:50996600-50997400	Enhancers	Pancreatic Islets	Pancreatic Islet
49	chr2:50996800-50997000	Enhancers	Cortex derived primary cultured neurospheres	brain
50	chr2:50996800-50997000	Active TSS	Brain Anterior Caudate	brain

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