Variant report

Variant	nsv1009922
Chromosome Location	chr2:50890581-51012083
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	chr2:50955596-50955702	K562	blood:	n/a	n/a
2	CEBPB	chr2:50919241-50919557	IMR90	lung:	n/a	chr2:50919400-50919413 chr2:50919400-50919411
3	CEBPB	chr2:50952000-50952353	HepG2	liver:	n/a	n/a
4	CEBPB	chr2:50954382-50954517	HepG2	liver:	n/a	n/a
5	CEBPB	chr2:50951993-50952357	IMR90	lung:	n/a	n/a
6	CEBPB	chr2:50951301-50951586	HepG2	liver:	n/a	chr2:50951423-50951436 chr2:50951424-50951435
7	CEBPB	chr2:50919242-50919552	HepG2	liver:	n/a	chr2:50919400-50919413 chr2:50919400-50919411
8	CEBPB	chr2:50952036-50952291	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr2:51003545-51003679	IMR90	lung:	n/a	n/a
10	CEBPB	chr2:50890728-50891191	HepG2	liver:	n/a	chr2:50890749-50890760 chr2:50891044-50891055
11	CEBPB	chr2:50974968-50975018	HepG2	liver:	n/a	n/a
12	CEBPB	chr2:50919262-50919518	K562	blood:	n/a	chr2:50919400-50919413 chr2:50919400-50919411
13	CEBPB	chr2:50952033-50952347	A549	lung:	n/a	n/a
14	CHD2	chr2:50947884-50948198	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr2:50902100-50902250	GM12864	blood:	n/a	n/a
16	CTCF	chr2:50901960-50902110	RPTEC	kidney:	n/a	n/a
17	CTCF	chr2:50973740-50973890	HepG2	liver:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
18	CTCF	chr2:50906100-50906250	GM12864	blood:	n/a	n/a
19	CTCF	chr2:50902106-50902258	A549	lung:	n/a	n/a
20	CTCF	chr2:50973720-50973870	GM12866	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
21	CTCF	chr2:50902100-50902250	HCPEpiC	choroid plexus:	n/a	n/a
22	CTCF	chr2:50973780-50973930	BE2_C	brain:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
23	CTCF	chr2:50973687-50973983	Gliobla	brain:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
24	CTCF	chr2:50902200-50902350	HRPEpiC	eye:	n/a	n/a
25	CTCF	chr2:50973783-50973941	GM13976	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
26	CTCF	chr2:50902080-50902230	HCPEpiC	choroid plexus:	n/a	n/a
27	CTCF	chr2:50973800-50973950	GM12870	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
28	CTCF	chr2:50902200-50902350	HRE	kidney:	n/a	n/a
29	CTCF	chr2:50973733-50973949	ProgFib	skin:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
30	CTCF	chr2:50973731-50973929	LNCaP	prostate:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
31	CTCF	chr2:50973704-50973959	H1-hESC	embryonic stem cell:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
32	CTCF	chr2:50973780-50973930	HCPEpiC	choroid plexus:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
33	CTCF	chr2:50902120-50902270	HepG2	liver:	n/a	n/a
34	CTCF	chr2:50902320-50902470	A549	lung:	n/a	n/a
35	CTCF	chr2:50973740-50973890	GM12867	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
36	CTCF	chr2:50973752-50973928	H1-hESC	embryonic stem cell:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
37	CTCF	chr2:50973760-50973923	K562	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
38	CTCF	chr2:50973760-50973910	RPTEC	kidney:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
39	CTCF	chr2:50978582-50978614	Kidney_OC	kidney:	n/a	n/a
40	CTCF	chr2:50973800-50973950	GM12869	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
41	CTCF	chr2:50902139-50902314	GM12891	blood:	n/a	n/a
42	CTCF	chr2:50973740-50973931	GM10266	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
43	CTCF	chr2:50902046-50902364	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr2:50902080-50902230	GM12873	blood:	n/a	n/a
45	CTCF	chr2:50902080-50902230	GM12864	blood:	n/a	n/a
46	CTCF	chr2:50902100-50902250	HepG2	liver:	n/a	n/a
47	CTCF	chr2:50973721-50973966	HepG2	liver:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
48	CTCF	chr2:50973420-50973570	HCM	heart:	n/a	n/a
49	CTCF	chr2:50973840-50973990	GM12869	blood:	n/a	chr2:50973841-50973849
50	CTCF	chr2:50973760-50973910	HPAF	blood vessel:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:50956659-50956709	NB4	blood:	n/a
2	chr2:50992829-50992879	GM12878	blood:	n/a
3	chr2:51001003-51001053	Hela-S3	cervix:	n/a
4	chr2:50956659-50956709	Jurkat	blood:	n/a
5	chr2:51001003-51001053	GM06990	blood:	n/a
6	chr2:50992829-50992879	GM19239	blood:	n/a
7	chr2:51001003-51001053	T-47D	breast:	n/a
8	chr2:50956659-50956709	HCF	heart:	n/a
9	chr2:51001003-51001053	U87	brain:	n/a
10	chr2:50956659-50956709	HMEC	breast:	n/a
11	chr2:51001003-51001053	HIPEpiC	eye:	n/a
12	chr2:50956659-50956709	HL-60	blood:	n/a
13	chr2:50956659-50956709	HRE	kidney:	n/a
14	chr2:50956659-50956709	K562	blood:	n/a
15	chr2:51001003-51001053	GM12892	blood:	n/a
16	chr2:51001003-51001053	BJ	skin:	n/a
17	chr2:51001003-51001053	HCF	heart:	n/a
18	chr2:51001003-51001053	CMK	blood:	n/a
19	chr2:51001003-51001053	GM12891	blood:	n/a
20	chr2:50956659-50956709	HCM	heart:	n/a
21	chr2:50956659-50956709	GM12892	blood:	n/a
22	chr2:50956659-50956709	HEEpiC	esophagus:	n/a
23	chr2:50992829-50992879	T-47D	breast:	n/a
24	chr2:50956659-50956709	HUVEC	blood vessel:	n/a
25	chr2:50992829-50992879	SKMC	muscle:	n/a
26	chr2:50956659-50956709	AoSMC	blood vessel:	n/a
27	chr2:51001003-51001053	HMEC	breast:	n/a
28	chr2:51001003-51001053	NB4	blood:	n/a
29	chr2:50992829-50992879	NB4	blood:	n/a
30	chr2:51001003-51001053	AG09309	skin:	n/a
31	chr2:50992829-50992879	LNCaP	prostate:	n/a
32	chr2:51001003-51001053	HepG2	liver:	n/a
33	chr2:50992829-50992879	AG09309	skin:	n/a
34	chr2:50956659-50956709	ovcar-3	ovarian:	n/a
35	chr2:51001003-51001053	AoSMC	blood vessel:	n/a
36	chr2:51001003-51001053	NHDF-neo	bronchial:	n/a
37	chr2:50956659-50956709	IMR90	lung:	fetal
38	chr2:51001003-51001053	SK-N-SH_RA	brain:	n/a
39	chr2:50992829-50992879	MCF-7	breast:	n/a
40	chr2:50992829-50992879	HNPCEpiC	eye:	n/a
41	chr2:50992829-50992879	HRE	kidney:	n/a
42	chr2:50992829-50992879	HRCEpiC	kidney:	n/a
43	chr2:50956659-50956709	BE2_C	brain:	n/a
44	chr2:50956659-50956709	Caco-2	colon:	n/a
45	chr2:50992829-50992879	PANC-1	pancreas:	n/a
46	chr2:50956659-50956709	MCF-7	breast:	n/a
47	chr2:50956659-50956709	SK-N-SH_RA	brain:	n/a
48	chr2:50992829-50992879	ovcar-3	ovarian:	n/a
49	chr2:50992829-50992879	ProgFib	skin:	n/a
50	chr2:51001003-51001053	HRE	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:50973459..50974271-chr2:52224493..52225477,4	MCF-7	breast:
2	chr2:50965713..50967269-chr2:50975937..50978033,2	K562	blood:
3	chr2:50977335..50979735-chr2:50992909..50995322,2	K562	blood:
4	chr2:50985182..50988156-chr2:50995412..50998213,2	K562	blood:
5	chr2:50909775..50912434-chr2:50920496..50923402,2	MCF-7	breast:
6	chr2:50946676..50947176-chr20:60981159..60981778,2	MCF-7	breast:
7	chr2:50965713..50967269-chr2:50975937..50978033,2	K562	blood:
8	chr2:50977335..50979735-chr2:50992909..50995322,2	K562	blood:
9	chr2:50985182..50988156-chr2:50995412..50998213,2	K562	blood:

Variant related genes	Relation type
ENSG00000216191	TF binding region
ENSG00000216191	CpG island
ENSG00000216191	chromatin interactions

Extended variants
information (count: 4140 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:4140 , 50 per page) page: 1 2 3 4 5 6 7 ... 83

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536244611	chr2:50890592-50890593	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs574733528	chr2:50890617-50890618	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs139954698	chr2:50890666-50890667	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs556343151	chr2:50890667-50890668	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs557089039	chr2:50890675-50890676	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs574746488	chr2:50890735-50890736	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs17040926	chr2:50890766-50890767	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs145054055	chr2:50890794-50890795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs569632013	chr2:50890804-50890805	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs545849279	chr2:50890817-50890818	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs370256553	chr2:50890849-50890850	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs538863503	chr2:50890858-50890859	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs558436425	chr2:50890887-50890888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs528069197	chr2:50890932-50890933	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs373330990	chr2:50890968-50890969	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs540578663	chr2:50890981-50890982	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs59075821	chr2:50890992-50890993	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs543897406	chr2:50890993-50890994	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs112627784	chr2:50891012-50891013	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs572324569	chr2:50891024-50891025	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs561952515	chr2:50891060-50891061	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs376577737	chr2:50891103-50891104	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs529161268	chr2:50891155-50891156	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs550797392	chr2:50891167-50891168	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs569002936	chr2:50891169-50891170	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs530922583	chr2:50891219-50891220	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs183092107	chr2:50891238-50891239	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs554551819	chr2:50891249-50891250	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs570784151	chr2:50891257-50891258	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs534690044	chr2:50891286-50891287	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs374078520	chr2:50891293-50891294	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs552910687	chr2:50891308-50891309	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs147550530	chr2:50891355-50891356	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs535723476	chr2:50891356-50891357	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs557288282	chr2:50891390-50891391	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs575779384	chr2:50891400-50891401	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs574531454	chr2:50891422-50891423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs545610309	chr2:50891426-50891427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs113311143	chr2:50891478-50891479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs112383879	chr2:50891485-50891486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs71411512	chr2:50891530-50891531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs35702112	chr2:50891576-50891577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs56969621	chr2:50891577-50891578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs572789968	chr2:50891580-50891581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs540241881	chr2:50891585-50891586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs142076151	chr2:50891590-50891591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs561620257	chr2:50891610-50891611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs563811958	chr2:50891613-50891614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs529225489	chr2:50891623-50891624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs145903672	chr2:50891624-50891625	Weak transcription	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
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
Acute myeloid leukemia	20729466	CNVD
Bipolar disorder	19114987	CNVD
Autism	20841430	CNVD
Schizophrenia	20967226	CNVD

Chromatin state (count:525 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:50886800-50890600	Weak transcription	NHEK	skin
2	chr2:50888400-50890800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr2:50889400-50890800	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr2:50890400-50890800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr2:50890400-50899200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr2:50890600-50891400	Enhancers	NHEK	skin
7	chr2:50890800-50891000	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr2:50890800-50895000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr2:50894800-50895800	Enhancers	Brain Angular Gyrus	brain
10	chr2:50895000-50895200	Enhancers	Brain Germinal Matrix	brain
11	chr2:50895000-50895600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr2:50895000-50895800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr2:50895200-50896200	Enhancers	Brain Substantia Nigra	brain
14	chr2:50895600-50896000	Enhancers	Brain Cingulate Gyrus	brain
15	chr2:50895800-50896000	Enhancers	Brain Germinal Matrix	brain
16	chr2:50896000-50896400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr2:50899200-50899600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr2:50899200-50899800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr2:50899600-50899800	Enhancers	Pancreatic Islets	Pancreatic Islet
20	chr2:50904200-50904600	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr2:50905400-50905800	Enhancers	Brain Hippocampus Middle	brain
22	chr2:50905600-50906200	Enhancers	Brain Anterior Caudate	brain
23	chr2:50905800-50906200	Enhancers	Brain Inferior Temporal Lobe	brain
24	chr2:50913400-50914000	Enhancers	Brain Angular Gyrus	brain
25	chr2:50913400-50914600	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr2:50913600-50914800	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr2:50913600-50916000	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr2:50913600-50916200	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr2:50913800-50915800	Enhancers	Brain Anterior Caudate	brain
30	chr2:50913800-50916200	Enhancers	H1 Cell Line	embryonic stem cell
31	chr2:50914000-50914200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr2:50914000-50914200	Enhancers	Brain Cingulate Gyrus	brain
33	chr2:50914000-50914400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr2:50914000-50917800	Weak transcription	Brain Angular Gyrus	brain
35	chr2:50914200-50915200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr2:50914200-50916000	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr2:50914200-50918600	Weak transcription	Brain Cingulate Gyrus	brain
38	chr2:50914400-50918400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr2:50914600-50914800	Enhancers	H9 Cell Line	embryonic stem cell
40	chr2:50914600-50914800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
41	chr2:50914600-50915200	Enhancers	Fetal Heart	heart
42	chr2:50914800-50915200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
43	chr2:50914800-50915200	Active TSS	iPS-20b Cell Line	embryonic stem cell
44	chr2:50914800-50915800	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr2:50915000-50915200	Enhancers	Brain Substantia Nigra	brain
46	chr2:50915000-50915400	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr2:50915000-50915600	Weak transcription	H9 Cell Line	embryonic stem cell
48	chr2:50915200-50915600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
49	chr2:50915200-50915800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr2:50915200-50916000	Enhancers	HUES48 Cell Line	embryonic stem cell

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