Variant report

Variant	nsv1005293
Chromosome Location	chr2:50914047-51066819
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	chr2:50919262-50919518	K562	blood:	n/a	chr2:50919400-50919413 chr2:50919400-50919411
3	CEBPB	chr2:50919242-50919552	HepG2	liver:	n/a	chr2:50919400-50919413 chr2:50919400-50919411
4	CEBPB	chr2:51042035-51042364	HepG2	liver:	n/a	chr2:51042175-51042186
5	CEBPB	chr2:50952000-50952353	HepG2	liver:	n/a	n/a
6	CEBPB	chr2:51042082-51042350	A549	lung:	n/a	chr2:51042175-51042186
7	CEBPB	chr2:51003545-51003679	IMR90	lung:	n/a	n/a
8	CEBPB	chr2:51051532-51051664	HepG2	liver:	n/a	chr2:51051618-51051629 chr2:51051616-51051627 chr2:51051616-51051629
9	CEBPB	chr2:50952036-50952291	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr2:50974968-50975018	HepG2	liver:	n/a	n/a
11	CEBPB	chr2:51039958-51040191	HepG2	liver:	n/a	n/a
12	CEBPB	chr2:50951301-50951586	HepG2	liver:	n/a	chr2:50951423-50951436 chr2:50951424-50951435
13	CEBPB	chr2:50951993-50952357	IMR90	lung:	n/a	n/a
14	CEBPB	chr2:50952033-50952347	A549	lung:	n/a	n/a
15	CEBPB	chr2:50954382-50954517	HepG2	liver:	n/a	n/a
16	CEBPB	chr2:50919241-50919557	IMR90	lung:	n/a	chr2:50919400-50919413 chr2:50919400-50919411
17	CHD2	chr2:51020103-51020131	GM12878	blood:	n/a	n/a
18	CHD2	chr2:50947884-50948198	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr2:50973687-50973983	Gliobla	brain:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
20	CTCF	chr2:51013607-51013764	Kidney_OC	kidney:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
21	CTCF	chr2:51013623-51013763	Hela-S3	cervix:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
22	CTCF	chr2:50973760-50973910	AG04450	lung:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
23	CTCF	chr2:50973772-50973922	GM19239	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
24	CTCF	chr2:50973780-50973930	HCT-116	colon:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
25	CTCF	chr2:50973780-50973930	SK-N-SH_RA	brain:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
26	CTCF	chr2:50973100-50973250	HCPEpiC	choroid plexus:	n/a	n/a
27	CTCF	chr2:50973740-50973890	WERI-Rb-1	eye:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
28	CTCF	chr2:51040238-51040274	A549	lung:	n/a	n/a
29	CTCF	chr2:50973740-50973890	GM12867	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
30	CTCF	chr2:50973740-50973890	AoAF	blood vessel:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
31	CTCF	chr2:50973740-50973890	RPTEC	kidney:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
32	CTCF	chr2:50973760-50973910	HCT-116	colon:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
33	CTCF	chr2:51013600-51013750	HepG2	liver:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
34	CTCF	chr2:50969658-50969686	MCF-7	breast:	n/a	n/a
35	CTCF	chr2:50973740-50973890	NHEK	skin:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
36	CTCF	chr2:50973760-50973923	K562	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
37	CTCF	chr2:51009720-51009870	AG04450	lung:	n/a	chr2:51009841-51009854
38	CTCF	chr2:50973634-50974016	HCT-116	colon:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
39	CTCF	chr2:50973739-50973958	LNCaP	prostate:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
40	CTCF	chr2:50973780-50973930	GM12873	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
41	CTCF	chr2:50973760-50973910	GM12864	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
42	CTCF	chr2:50973780-50973930	WI-38	lung:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
43	CTCF	chr2:50973740-50973890	HepG2	liver:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
44	CTCF	chr2:50973740-50973890	Caco-2	colon:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
45	CTCF	chr2:51013620-51013770	HCT-116	colon:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
46	CTCF	chr2:50973783-50973941	GM13976	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
47	CTCF	chr2:50973751-50973938	GM12892	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
48	CTCF	chr2:50973717-50973974	GM12878	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
49	CTCF	chr2:50973780-50973930	HEK293	kidney:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
50	CTCF	chr2:50973708-50973972	MCF-7	breast:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:50992829-50992879	HCF	heart:	n/a
2	chr2:51001003-51001053	ECC-1	luminal epithelium:	n/a
3	chr2:50992829-50992879	HCF	heart:	n/a
4	chr2:51001003-51001053	ECC-1	luminal epithelium:	n/a
5	chr2:50992829-50992879	PrEC	prostate:	n/a
6	chr2:51056822-51056872	T-47D	breast:	n/a
7	chr2:51065673-51065723	AG09309	skin:	n/a
8	chr2:51057548-51057598	MCF10A-Er-Src	breast:	n/a
9	chr2:51056822-51056872	PANC-1	pancreas:	n/a
10	chr2:51056884-51056934	HAEpiC	amniotic membrane:	n/a
11	chr2:51056884-51056934	LNCaP	prostate:	n/a
12	chr2:51057218-51057268	HPAEpiC	pulmonary alveolar:	n/a
13	chr2:51056884-51056934	PrEC	prostate:	n/a
14	chr2:51001003-51001053	NH-A	brain:	n/a
15	chr2:50992829-50992879	K562	blood:	n/a
16	chr2:50956659-50956709	AG10803	skin:	n/a
17	chr2:51057218-51057268	SKMC	muscle:	n/a
18	chr2:51001003-51001053	HPAEpiC	pulmonary alveolar:	n/a
19	chr2:50956659-50956709	PrEC	prostate:	n/a
20	chr2:50956659-50956709	AG04450	lung:	fetal
21	chr2:51057548-51057598	HUVEC	blood vessel:	n/a
22	chr2:51056884-51056934	Hepatocyte	liver:	n/a
23	chr2:51065673-51065723	MCF10A-Er-Src	breast:	n/a
24	chr2:51057218-51057268	ECC-1	luminal epithelium:	n/a
25	chr2:51057218-51057268	Caco-2	colon:	n/a
26	chr2:51057548-51057598	H1-hESC	embryonic stem cell:	embryo
27	chr2:51056884-51056934	SK-N-SH	brain:	n/a
28	chr2:51057548-51057598	AG09309	skin:	n/a
29	chr2:51056884-51056934	GM12878	blood:	n/a
30	chr2:51057548-51057598	HEEpiC	esophagus:	n/a
31	chr2:51001003-51001053	MCF-7	breast:	n/a
32	chr2:50992829-50992879	HNPCEpiC	eye:	n/a
33	chr2:51001003-51001053	HAEpiC	amniotic membrane:	n/a
34	chr2:50992829-50992879	GM06990	blood:	n/a
35	chr2:50992829-50992879	LNCaP	prostate:	n/a
36	chr2:51001003-51001053	CMK	blood:	n/a
37	chr2:51057218-51057268	HRCEpiC	kidney:	n/a
38	chr2:51057548-51057598	HCM	heart:	n/a
39	chr2:50992829-50992879	RPTEC	kidney:	n/a
40	chr2:51057548-51057598	HNPCEpiC	eye:	n/a
41	chr2:50956659-50956709	NHDF-neo	bronchial:	n/a
42	chr2:50956659-50956709	GM12891	blood:	n/a
43	chr2:51065673-51065723	HCT-116	colon:	n/a
44	chr2:51057548-51057598	GM12878	blood:	n/a
45	chr2:51065673-51065723	H1-hESC	embryonic stem cell:	embryo
46	chr2:51056884-51056934	HPAEpiC	pulmonary alveolar:	n/a
47	chr2:51001003-51001053	HepG2	liver:	n/a
48	chr2:51056884-51056934	BE2_C	brain:	n/a
49	chr2:51065673-51065723	AG10803	skin:	n/a
50	chr2:51001003-51001053	AG10803	skin:	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	chr2:50973459..50974271-chr2:52224493..52225477,4	MCF-7	breast:
4	chr2:51018306..51019906-chr2:51022210..51025087,2	K562	blood:
5	chr2:50946676..50947176-chr20:60981159..60981778,2	MCF-7	breast:
6	chr2:50965713..50967269-chr2:50975937..50978033,2	K562	blood:
7	chr2:50977335..50979735-chr2:50992909..50995322,2	K562	blood:
8	chr2:51018306..51019906-chr2:51022210..51025087,2	K562	blood:
9	chr2:50985182..50988156-chr2:50995412..50998213,2	K562	blood:
10	chr2:50985182..50988156-chr2:50995412..50998213,2	K562	blood:

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

Variant related genes	Relation type
ENSG00000216191	TF binding region
ENSG00000238165	TF binding region
ENSG00000215968	TF binding region
ENSG00000216191	CpG island
ENSG00000238165	CpG island
ENSG00000215968	CpG island

Extended variants
information (count: 5468 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:5468 , 50 per page) page: 1 2 3 4 5 6 7 ... 110

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs183698338	chr2:50914067-50914068	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs561390952	chr2:50914083-50914084	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs531678321	chr2:50914106-50914107	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs550184833	chr2:50914111-50914112	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs571546367	chr2:50914166-50914167	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs532880348	chr2:50914169-50914170	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs550089223	chr2:50914178-50914179	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs547693747	chr2:50914190-50914191	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs565985699	chr2:50914207-50914208	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs537686983	chr2:50914225-50914226	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs554705457	chr2:50914242-50914243	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs370971377	chr2:50914291-50914292	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs188840950	chr2:50914303-50914304	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs570342888	chr2:50914307-50914308	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs191775670	chr2:50914334-50914335	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs532664864	chr2:50914340-50914341	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs185185811	chr2:50914344-50914345	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs553308018	chr2:50914359-50914360	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs551358321	chr2:50914364-50914365	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs574757790	chr2:50914410-50914411	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs542062637	chr2:50914458-50914459	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs375503548	chr2:50914474-50914475	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs563458731	chr2:50914479-50914480	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs918808	chr2:50914485-50914486	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs190080090	chr2:50914518-50914519	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs543541564	chr2:50914570-50914571	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs565340048	chr2:50914585-50914586	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs532404828	chr2:50914629-50914630	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs371340334	chr2:50914635-50914636	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs533164152	chr2:50914648-50914649	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs556034252	chr2:50914650-50914651	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs182195943	chr2:50914668-50914669	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs149756154	chr2:50914671-50914672	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs371970348	chr2:50914684-50914685	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs147430002	chr2:50914729-50914730	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs530312142	chr2:50914784-50914785	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs187269696	chr2:50914793-50914794	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs114566606	chr2:50914826-50914827	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs533728993	chr2:50914839-50914840	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs369545303	chr2:50914844-50914845	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs189248900	chr2:50914854-50914855	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs180974392	chr2:50914862-50914863	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs139901070	chr2:50914864-50914865	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs534343972	chr2:50914876-50914877	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs552970917	chr2:50914898-50914899	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs185036844	chr2:50914935-50914936	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs535727035	chr2:50915094-50915095	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs553956520	chr2:50915139-50915140	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs577862260	chr2:50915144-50915145	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs557232594	chr2:50915172-50915173	Enhancers Weak transcription Flanking Active TSS Active TSS	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:636 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:50913400-50914600	Enhancers	iPS-20b Cell Line	embryonic stem cell
2	chr2:50913600-50914800	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr2:50913600-50916000	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr2:50913600-50916200	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr2:50913800-50915800	Enhancers	Brain Anterior Caudate	brain
6	chr2:50913800-50916200	Enhancers	H1 Cell Line	embryonic stem cell
7	chr2:50914000-50914200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr2:50914000-50914200	Enhancers	Brain Cingulate Gyrus	brain
9	chr2:50914000-50914400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr2:50914000-50917800	Weak transcription	Brain Angular Gyrus	brain
11	chr2:50914200-50915200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr2:50914200-50916000	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr2:50914200-50918600	Weak transcription	Brain Cingulate Gyrus	brain
14	chr2:50914400-50918400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr2:50914600-50914800	Enhancers	H9 Cell Line	embryonic stem cell
16	chr2:50914600-50914800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
17	chr2:50914600-50915200	Enhancers	Fetal Heart	heart
18	chr2:50914800-50915200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
19	chr2:50914800-50915200	Active TSS	iPS-20b Cell Line	embryonic stem cell
20	chr2:50914800-50915800	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr2:50915000-50915200	Enhancers	Brain Substantia Nigra	brain
22	chr2:50915000-50915400	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr2:50915000-50915600	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr2:50915200-50915600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
25	chr2:50915200-50915800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr2:50915200-50916000	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr2:50915600-50915800	Enhancers	H9 Cell Line	embryonic stem cell
28	chr2:50915600-50916000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr2:50915600-50916200	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr2:50915800-50917800	Weak transcription	Brain Anterior Caudate	brain
31	chr2:50915800-50918600	Weak transcription	HUES64 Cell Line	embryonic stem cell
32	chr2:50915800-50918800	Weak transcription	H9 Cell Line	embryonic stem cell
33	chr2:50916000-50918600	Weak transcription	HUES48 Cell Line	embryonic stem cell
34	chr2:50916000-50918800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
35	chr2:50916000-50948000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr2:50916200-50923800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
37	chr2:50917600-50917800	Enhancers	Brain Hippocampus Middle	brain
38	chr2:50917600-50918000	Weak transcription	Brain Substantia Nigra	brain
39	chr2:50917600-50918400	Enhancers	Brain Inferior Temporal Lobe	brain
40	chr2:50917800-50918400	Enhancers	Brain Angular Gyrus	brain
41	chr2:50917800-50918600	Enhancers	Brain Anterior Caudate	brain
42	chr2:50918000-50918200	Enhancers	Brain Substantia Nigra	brain
43	chr2:50918200-50918800	Weak transcription	Brain Substantia Nigra	brain
44	chr2:50918400-50918600	Weak transcription	Brain Inferior Temporal Lobe	brain
45	chr2:50918400-50918800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr2:50918400-50919200	Active TSS	Brain Angular Gyrus	brain
47	chr2:50918400-50919600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr2:50918600-50918800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr2:50918600-50919200	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr2:50918600-50919200	Enhancers	HUES64 Cell Line	embryonic stem cell

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