Variant report

Variant	nsv1001190
Chromosome Location	chr2:50955013-51040820
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	chr2:51003545-51003679	IMR90	lung:	n/a	n/a
3	CEBPB	chr2:51039958-51040191	HepG2	liver:	n/a	n/a
4	CEBPB	chr2:50974968-50975018	HepG2	liver:	n/a	n/a
5	CHD2	chr2:51020103-51020131	GM12878	blood:	n/a	n/a
6	CTCF	chr2:51013620-51013770	HCT-116	colon:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
7	CTCF	chr2:50973554-50974218	SK-N-SH	brain:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
8	CTCF	chr2:50973740-50973890	WERI-Rb-1	eye:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
9	CTCF	chr2:50973740-50973890	NHEK	skin:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
10	CTCF	chr2:50973760-50973910	HA-sp	spinal cord:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
11	CTCF	chr2:51013580-51013730	WERI-Rb-1	eye:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
12	CTCF	chr2:51013660-51013810	GM12873	blood:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
13	CTCF	chr2:50973740-50973890	NB4	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
14	CTCF	chr2:50973520-50973670	HepG2	liver:	n/a	n/a
15	CTCF	chr2:50973800-50973950	MCF-7	breast:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
16	CTCF	chr2:50973733-50973905	A549	lung:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
17	CTCF	chr2:50973780-50973930	GM12873	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
18	CTCF	chr2:50973752-50973913	GM10248	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
19	CTCF	chr2:50973572-50973669	Gliobla	brain:	n/a	n/a
20	CTCF	chr2:50969658-50969686	MCF-7	breast:	n/a	n/a
21	CTCF	chr2:50973722-50973924	SK-N-SH_RA	brain:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
22	CTCF	chr2:50973740-50973890	GM12871	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
23	CTCF	chr2:50973740-50973890	HRE	kidney:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
24	CTCF	chr2:50973708-50973972	MCF-7	breast:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
25	CTCF	chr2:50973780-50973930	HRPEpiC	eye:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
26	CTCF	chr2:50973740-50973890	GM12870	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
27	CTCF	chr2:50973720-50973870	HEK293	kidney:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
28	CTCF	chr2:50973740-50973890	HEEpiC	esophagus:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
29	CTCF	chr2:50973772-50973922	GM19239	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
30	CTCF	chr2:50973705-50973962	Hela-S3	cervix:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
31	CTCF	chr2:50973760-50973910	GM12871	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
32	CTCF	chr2:50973751-50973938	GM12892	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
33	CTCF	chr2:50973760-50973910	RPTEC	kidney:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
34	CTCF	chr2:50973795-50973920	Spleen_OC	spleen:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
35	CTCF	chr2:50973622-50974108	MCF-7	breast:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
36	CTCF	chr2:50973100-50973250	HCPEpiC	choroid plexus:	n/a	n/a
37	CTCF	chr2:50973746-50973940	MCF-7	breast:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
38	CTCF	chr2:50976420-50976570	Caco-2	colon:	n/a	n/a
39	CTCF	chr2:50973780-50973930	HMEC	breast:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
40	CTCF	chr2:50973760-50973910	GM12872	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
41	CTCF	chr2:51013620-51013770	WERI-Rb-1	eye:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
42	CTCF	chr2:50973800-50973950	GM06990	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
43	CTCF	chr2:51009720-51009870	AG04450	lung:	n/a	chr2:51009841-51009854
44	CTCF	chr2:50978500-50978650	BE2_C	brain:	n/a	n/a
45	CTCF	chr2:50973732-50973965	GM19238	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
46	CTCF	chr2:50973740-50973890	AG09319	gingival:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
47	CTCF	chr2:51013640-51013790	RPTEC	kidney:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
48	CTCF	chr2:50973780-50973930	HCM	heart:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
49	CTCF	chr2:50973720-50973870	HPF	lung:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
50	CTCF	chr2:50973420-50973570	HCM	heart:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:50956659-50956709	T-47D	breast:	n/a
2	chr2:51001003-51001053	HNPCEpiC	eye:	n/a
3	chr2:50956659-50956709	Hepatocyte	liver:	n/a
4	chr2:51001003-51001053	Hepatocyte	liver:	n/a
5	chr2:50956659-50956709	LNCaP	prostate:	n/a
6	chr2:51001003-51001053	GM06990	blood:	n/a
7	chr2:51001003-51001053	ECC-1	luminal epithelium:	n/a
8	chr2:50992829-50992879	ProgFib	skin:	n/a
9	chr2:50956659-50956709	A549	lung:	n/a
10	chr2:50992829-50992879	MCF10A-Er-Src	breast:	n/a
11	chr2:50992829-50992879	MCF-7	breast:	n/a
12	chr2:51001003-51001053	NHDF-neo	bronchial:	n/a
13	chr2:51001003-51001053	HCF	heart:	n/a
14	chr2:51001003-51001053	ProgFib	skin:	n/a
15	chr2:50992829-50992879	HUVEC	blood vessel:	n/a
16	chr2:50992829-50992879	AG04450	lung:	fetal
17	chr2:50956659-50956709	Jurkat	blood:	n/a
18	chr2:50992829-50992879	AoSMC	blood vessel:	n/a
19	chr2:51001003-51001053	HPAEpiC	pulmonary alveolar:	n/a
20	chr2:50992829-50992879	U87	brain:	n/a
21	chr2:50992829-50992879	T-47D	breast:	n/a
22	chr2:50992829-50992879	PFSK-1	brain:	n/a
23	chr2:50956659-50956709	NHDF-neo	bronchial:	n/a
24	chr2:51001003-51001053	A549	lung:	n/a
25	chr2:51001003-51001053	SAEC	small airway:	n/a
26	chr2:51001003-51001053	HEEpiC	esophagus:	n/a
27	chr2:50992829-50992879	NHDF-neo	bronchial:	n/a
28	chr2:50992829-50992879	HEK293	kidney:	embryo
29	chr2:51001003-51001053	HCT-116	colon:	n/a
30	chr2:50992829-50992879	HRCEpiC	kidney:	n/a
31	chr2:50992829-50992879	HNPCEpiC	eye:	n/a
32	chr2:50992829-50992879	HRPEpiC	eye:	n/a
33	chr2:51001003-51001053	SK-N-SH	brain:	n/a
34	chr2:51001003-51001053	PFSK-1	brain:	n/a
35	chr2:51001003-51001053	H1-hESC	embryonic stem cell:	embryo
36	chr2:51001003-51001053	CMK	blood:	n/a
37	chr2:50956659-50956709	HRPEpiC	eye:	n/a
38	chr2:51001003-51001053	HepG2	liver:	n/a
39	chr2:50992829-50992879	CMK	blood:	n/a
40	chr2:50956659-50956709	HL-60	blood:	n/a
41	chr2:51001003-51001053	GM19239	blood:	n/a
42	chr2:51001003-51001053	GM12891	blood:	n/a
43	chr2:50956659-50956709	HRCEpiC	kidney:	n/a
44	chr2:51001003-51001053	HRCEpiC	kidney:	n/a
45	chr2:50992829-50992879	Jurkat	blood:	n/a
46	chr2:51001003-51001053	Jurkat	blood:	n/a
47	chr2:51001003-51001053	NH-A	brain:	n/a
48	chr2:51001003-51001053	MCF10A-Er-Src	breast:	n/a
49	chr2:51001003-51001053	AG10803	skin:	n/a
50	chr2:50992829-50992879	NHBE	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:50977335..50979735-chr2:50992909..50995322,2	K562	blood:
2	chr2:50965713..50967269-chr2:50975937..50978033,2	K562	blood:
3	chr2:50985182..50988156-chr2:50995412..50998213,2	K562	blood:
4	chr2:50977335..50979735-chr2:50992909..50995322,2	K562	blood:
5	chr2:50985182..50988156-chr2:50995412..50998213,2	K562	blood:
6	chr2:51018306..51019906-chr2:51022210..51025087,2	K562	blood:
7	chr2:51018306..51019906-chr2:51022210..51025087,2	K562	blood:
8	chr2:50973459..50974271-chr2:52224493..52225477,4	MCF-7	breast:
9	chr2:50965713..50967269-chr2:50975937..50978033,2	K562	blood:

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

Extended variants
information (count: 2764 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:2764 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs572821382	chr2:50955014-50955015	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs550006276	chr2:50955015-50955016	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs571428378	chr2:50955045-50955046	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs371179325	chr2:50955046-50955047	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs184299349	chr2:50955071-50955072	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs542009221	chr2:50955151-50955152	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs558204827	chr2:50955153-50955154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs566782194	chr2:50955184-50955185	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs534182138	chr2:50955218-50955219	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs190022474	chr2:50955231-50955232	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs573997450	chr2:50955247-50955248	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs374918351	chr2:50955252-50955253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs375819432	chr2:50955294-50955295	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs544461395	chr2:50955302-50955303	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs548104760	chr2:50955328-50955329	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs556352803	chr2:50955332-50955333	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs34985596	chr2:50955347-50955348	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs530433414	chr2:50955381-50955382	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs544801660	chr2:50955531-50955532	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs544561070	chr2:50955536-50955537	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs560174235	chr2:50955539-50955540	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs571983452	chr2:50955544-50955545	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs542645026	chr2:50955562-50955563	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs181087448	chr2:50955566-50955567	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs531650774	chr2:50955577-50955578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs550067451	chr2:50955604-50955605	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs564955947	chr2:50955613-50955614	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs199634803	chr2:50955635-50955636	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs560571932	chr2:50955693-50955694	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs551617532	chr2:50955715-50955716	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs187001287	chr2:50955737-50955738	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs533989376	chr2:50955744-50955745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs533396317	chr2:50955830-50955831	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs548974865	chr2:50955964-50955965	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs190499642	chr2:50955976-50955977	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs116309115	chr2:50956057-50956058	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs556416455	chr2:50956071-50956072	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs933734	chr2:50956081-50956082	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs578134197	chr2:50956085-50956086	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs539210715	chr2:50956119-50956120	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs933735	chr2:50956133-50956134	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs553630253	chr2:50956219-50956220	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs374739286	chr2:50956222-50956223	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs572111679	chr2:50956282-50956283	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs540227413	chr2:50956287-50956288	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs542706567	chr2:50956293-50956294	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs560659356	chr2:50956338-50956339	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs115638097	chr2:50956360-50956361	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs140743481	chr2:50956372-50956373	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs529325014	chr2:50956391-50956392	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:106)

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
Autism	20841430	CNVD
Schizophrenia	20967226	CNVD

Chromatin state (count:351 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:50948400-50957000	Weak transcription	Fetal Brain Male	brain
2	chr2:50948600-50956400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr2:50948600-50956600	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr2:50948600-50956600	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr2:50948800-50955200	Weak transcription	Fetal Brain Female	brain
6	chr2:50951000-50956600	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr2:50951200-50955400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
8	chr2:50951200-50956400	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr2:50951200-50956400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
10	chr2:50951200-50956400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr2:50951200-50959800	Weak transcription	Brain Anterior Caudate	brain
12	chr2:50951400-50956800	Weak transcription	Brain Cingulate Gyrus	brain
13	chr2:50952400-50956200	Enhancers	Pancreatic Islets	Pancreatic Islet
14	chr2:50952400-50957000	Weak transcription	Cortex derived primary cultured neurospheres	brain
15	chr2:50954800-50957400	Enhancers	Brain Germinal Matrix	brain
16	chr2:50955000-50955600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr2:50955000-50955800	Enhancers	Brain Angular Gyrus	brain
18	chr2:50955000-50955800	Enhancers	HSMMtube	muscle
19	chr2:50955200-50957400	Enhancers	Fetal Brain Female	brain
20	chr2:50955400-50956000	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr2:50955600-50959800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr2:50955800-50956600	Weak transcription	Brain Angular Gyrus	brain
23	chr2:50955800-50956600	Weak transcription	HSMMtube	muscle
24	chr2:50956000-50956400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
25	chr2:50956200-50959400	Weak transcription	Pancreatic Islets	Pancreatic Islet
26	chr2:50956400-50956600	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
27	chr2:50956400-50957000	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr2:50956400-50957600	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr2:50956400-50957800	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr2:50956400-50957800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
31	chr2:50956600-50956800	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr2:50956600-50957000	Enhancers	H9 Cell Line	embryonic stem cell
33	chr2:50956600-50957000	Enhancers	Brain Angular Gyrus	brain
34	chr2:50956600-50957000	Enhancers	HSMMtube	muscle
35	chr2:50956600-50957200	Enhancers	H1 Cell Line	embryonic stem cell
36	chr2:50956600-50957200	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr2:50956600-50957400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr2:50956600-50957400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr2:50956600-50957600	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr2:50956800-50957000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
41	chr2:50956800-50957200	Enhancers	Brain Cingulate Gyrus	brain
42	chr2:50957000-50957200	Enhancers	Fetal Brain Male	brain
43	chr2:50957000-50957600	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr2:50957000-50957600	Enhancers	Cortex derived primary cultured neurospheres	brain
45	chr2:50959400-50960000	Enhancers	Pancreatic Islets	Pancreatic Islet
46	chr2:50959800-50960000	Enhancers	Brain Anterior Caudate	brain
47	chr2:50959800-50960200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr2:50960000-50961600	Weak transcription	Pancreatic Islets	Pancreatic Islet
49	chr2:50961600-50961800	Enhancers	Pancreatic Islets	Pancreatic Islet
50	chr2:50965400-50966200	Enhancers	Brain Germinal Matrix	brain

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