Variant report

Variant	nsv1014217
Chromosome Location	chr2:50906725-51099781
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	BACH1	chr2:50955596-50955702	K562	blood:	n/a	n/a
3	CEBPB	chr2:50952036-50952291	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr2:51051532-51051664	HepG2	liver:	n/a	chr2:51051618-51051629 chr2:51051616-51051627 chr2:51051616-51051629
5	CEBPB	chr2:50954382-50954517	HepG2	liver:	n/a	n/a
6	CEBPB	chr2:50919241-50919557	IMR90	lung:	n/a	chr2:50919400-50919413 chr2:50919400-50919411
7	CEBPB	chr2:50919262-50919518	K562	blood:	n/a	chr2:50919400-50919413 chr2:50919400-50919411
8	CEBPB	chr2:51077746-51078099	IMR90	lung:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
9	CEBPB	chr2:51084914-51085194	A549	lung:	n/a	chr2:51085060-51085071
10	CEBPB	chr2:51084918-51085221	HepG2	liver:	n/a	chr2:51085060-51085071
11	CEBPB	chr2:50952000-50952353	HepG2	liver:	n/a	n/a
12	CEBPB	chr2:51084911-51085196	IMR90	lung:	n/a	chr2:51085060-51085071
13	CEBPB	chr2:50919242-50919552	HepG2	liver:	n/a	chr2:50919400-50919413 chr2:50919400-50919411
14	CEBPB	chr2:51068879-51068992	HepG2	liver:	n/a	chr2:51068958-51068969
15	CEBPB	chr2:51080882-51081169	HepG2	liver:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
16	CEBPB	chr2:51077720-51078095	HepG2	liver:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
17	CEBPB	chr2:51077727-51078088	H1-hESC	embryonic stem cell:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
18	CEBPB	chr2:51077765-51078077	A549	lung:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
19	CEBPB	chr2:51042082-51042350	A549	lung:	n/a	chr2:51042175-51042186
20	CEBPB	chr2:51003545-51003679	IMR90	lung:	n/a	n/a
21	CEBPB	chr2:50952033-50952347	A549	lung:	n/a	n/a
22	CEBPB	chr2:51080893-51081164	Hela-S3	cervix:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
23	CEBPB	chr2:51080924-51081178	H1-hESC	embryonic stem cell:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
24	CEBPB	chr2:51084920-51085210	H1-hESC	embryonic stem cell:	n/a	chr2:51085060-51085071
25	CEBPB	chr2:50951993-50952357	IMR90	lung:	n/a	n/a
26	CEBPB	chr2:51077732-51078049	Hela-S3	cervix:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
27	CEBPB	chr2:51080929-51081152	A549	lung:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
28	CEBPB	chr2:50951301-50951586	HepG2	liver:	n/a	chr2:50951423-50951436 chr2:50951424-50951435
29	CEBPB	chr2:51042035-51042364	HepG2	liver:	n/a	chr2:51042175-51042186
30	CEBPB	chr2:51039958-51040191	HepG2	liver:	n/a	n/a
31	CEBPB	chr2:51080873-51081218	IMR90	lung:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
32	CEBPB	chr2:50974968-50975018	HepG2	liver:	n/a	n/a
33	CHD2	chr2:50947884-50948198	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr2:51020103-51020131	GM12878	blood:	n/a	n/a
35	CTCF	chr2:50973840-50973990	GM12869	blood:	n/a	chr2:50973841-50973849
36	CTCF	chr2:50973760-50973910	HPAF	blood vessel:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
37	CTCF	chr2:50978582-50978614	Kidney_OC	kidney:	n/a	n/a
38	CTCF	chr2:50973760-50973910	BE2_C	brain:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
39	CTCF	chr2:51008900-51009050	Caco-2	colon:	n/a	n/a
40	CTCF	chr2:51086380-51086530	HCT-116	colon:	n/a	n/a
41	CTCF	chr2:51013640-51013790	HRPEpiC	eye:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
42	CTCF	chr2:50973420-50973570	HCM	heart:	n/a	n/a
43	CTCF	chr2:50973760-50973910	Hela-S3	cervix:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
44	CTCF	chr2:50973705-50973915	A549	lung:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
45	CTCF	chr2:50973642-50974009	HepG2	liver:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
46	CTCF	chr2:51009804-51009856	Hela-S3	cervix:	n/a	chr2:51009841-51009854
47	CTCF	chr2:50973625-50974108	A549	lung:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
48	CTCF	chr2:50973760-50973910	BJ	skin:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
49	CTCF	chr2:50973740-50973890	GM12871	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
50	CTCF	chr2:50973687-50973983	Gliobla	brain:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:51057218-51057268	AG04450	lung:	fetal
2	chr2:50992829-50992879	NT2-D1	testis:	n/a
3	chr2:51001003-51001053	HMEC	breast:	n/a
4	chr2:51074881-51074931	H1-hESC	embryonic stem cell:	embryo
5	chr2:51074939-51074989	GM12891	blood:	n/a
6	chr2:51056822-51056872	BE2_C	brain:	n/a
7	chr2:50956659-50956709	HepG2	liver:	n/a
8	chr2:50992829-50992879	AG04449	skin:	fetal
9	chr2:51074939-51074989	AG04450	lung:	fetal
10	chr2:51074939-51074989	U87	brain:	n/a
11	chr2:51074939-51074989	PANC-1	pancreas:	n/a
12	chr2:51074939-51074989	NB4	blood:	n/a
13	chr2:51057548-51057598	GM12878	blood:	n/a
14	chr2:51057218-51057268	NHDF-neo	bronchial:	n/a
15	chr2:51074939-51074989	MCF-7	breast:	n/a
16	chr2:51074939-51074989	Hela-S3	cervix:	n/a
17	chr2:51056822-51056872	HRE	kidney:	n/a
18	chr2:51074939-51074989	HepG2	liver:	n/a
19	chr2:51074881-51074931	AG04449	skin:	fetal
20	chr2:51056822-51056872	T-47D	breast:	n/a
21	chr2:51001003-51001053	HUVEC	blood vessel:	n/a
22	chr2:51074939-51074989	NH-A	brain:	n/a
23	chr2:51056822-51056872	HUVEC	blood vessel:	n/a
24	chr2:51074881-51074931	HRPEpiC	eye:	n/a
25	chr2:51065673-51065723	AG09309	skin:	n/a
26	chr2:51074939-51074989	H1-hESC	embryonic stem cell:	embryo
27	chr2:51074939-51074989	HMEC	breast:	n/a
28	chr2:51057218-51057268	SK-N-MC	brain:	n/a
29	chr2:51057548-51057598	HNPCEpiC	eye:	n/a
30	chr2:51065673-51065723	HRCEpiC	kidney:	n/a
31	chr2:51074939-51074989	HUVEC	blood vessel:	n/a
32	chr2:51056822-51056872	Caco-2	colon:	n/a
33	chr2:51056884-51056934	HEK293	kidney:	embryo
34	chr2:51057548-51057598	U87	brain:	n/a
35	chr2:51057548-51057598	PrEC	prostate:	n/a
36	chr2:51074939-51074989	AG09309	skin:	n/a
37	chr2:51057218-51057268	HRPEpiC	eye:	n/a
38	chr2:51057218-51057268	HEK293	kidney:	embryo
39	chr2:51065673-51065723	HCM	heart:	n/a
40	chr2:51057548-51057598	IMR90	lung:	fetal
41	chr2:51057218-51057268	HL-60	blood:	n/a
42	chr2:51056884-51056934	K562	blood:	n/a
43	chr2:51074939-51074989	Hepatocyte	liver:	n/a
44	chr2:50992829-50992879	U87	brain:	n/a
45	chr2:51001003-51001053	Jurkat	blood:	n/a
46	chr2:51065673-51065723	SK-N-SH_RA	brain:	n/a
47	chr2:51057218-51057268	GM06990	blood:	n/a
48	chr2:51074939-51074989	LNCaP	prostate:	n/a
49	chr2:51074881-51074931	Hela-S3	cervix:	n/a
50	chr2:51056884-51056934	AG10803	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:51084150..51086897-chr2:51088805..51090362,2	K562	blood:
2	chr2:50909775..50912434-chr2:50920496..50923402,2	MCF-7	breast:
3	chr2:50965713..50967269-chr2:50975937..50978033,2	K562	blood:
4	chr2:50973459..50974271-chr2:52224493..52225477,4	MCF-7	breast:
5	chr2:50946676..50947176-chr20:60981159..60981778,2	MCF-7	breast:
6	chr2:51018306..51019906-chr2:51022210..51025087,2	K562	blood:
7	chr2:50985182..50988156-chr2:50995412..50998213,2	K562	blood:
8	chr2:50985182..50988156-chr2:50995412..50998213,2	K562	blood:
9	chr2:50965713..50967269-chr2:50975937..50978033,2	K562	blood:
10	chr2:51084150..51086897-chr2:51088805..51090362,2	K562	blood:
11	chr2:50977335..50979735-chr2:50992909..50995322,2	K562	blood:
12	chr2:51018306..51019906-chr2:51022210..51025087,2	K562	blood:
13	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
ENSG00000216191	TF binding region
ENSG00000238165	TF binding region
ENSG00000215968	TF binding region
ENSG00000216191	CpG island
ENSG00000238165	CpG island
ENSG00000215968	CpG island
ENSG00000216191	chromatin interactions

Extended variants
information (count: 6866 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:6866 , 50 per page) page: 1 2 3 4 5 6 7 ... 138

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs141061601	chr2:50909832-50909833	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs35313417	chr2:50909842-50909843	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs562631750	chr2:50909851-50909852	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs546096715	chr2:50909868-50909869	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs200423917	chr2:50909889-50909890	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs184268597	chr2:50909939-50909940	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs572940282	chr2:50909941-50909942	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs377701319	chr2:50909998-50909999	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs72887516	chr2:50910013-50910014	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs533667644	chr2:50910058-50910059	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs530108983	chr2:50910059-50910060	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs188906677	chr2:50910073-50910074	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs563329727	chr2:50910086-50910087	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs531138031	chr2:50910126-50910127	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs150235700	chr2:50910157-50910158	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs564742814	chr2:50910175-50910176	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs373305652	chr2:50910202-50910203	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs528688344	chr2:50910209-50910210	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs547143782	chr2:50910231-50910232	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs568176426	chr2:50910272-50910273	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs535526032	chr2:50910277-50910278	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs375701780	chr2:50910330-50910331	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs555069474	chr2:50910344-50910345	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs539759371	chr2:50910360-50910361	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs193242181	chr2:50910393-50910394	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs367824362	chr2:50910446-50910447	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs184527458	chr2:50910497-50910498	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs533772449	chr2:50910520-50910521	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs555110459	chr2:50910540-50910541	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs574629441	chr2:50910546-50910547	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs541900099	chr2:50910553-50910554	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs563389953	chr2:50910575-50910576	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs575224970	chr2:50910598-50910599	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs10469918	chr2:50910602-50910603	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs564646396	chr2:50910626-50910627	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs368927065	chr2:50910627-50910628	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs567106271	chr2:50910638-50910639	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs546910663	chr2:50910662-50910663	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs527348009	chr2:50910752-50910753	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs1964305	chr2:50910782-50910783	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs1964306	chr2:50910784-50910785	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs371672526	chr2:50910785-50910786	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs71225142	chr2:50910804-50910805	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs531760735	chr2:50910826-50910827	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs529043392	chr2:50910869-50910870	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs138954684	chr2:50910888-50910889	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs568929858	chr2:50910891-50910892	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs551470107	chr2:50910920-50910921	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs72887520	chr2:50910971-50910972	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs375919185	chr2:50910997-50910998	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:108)

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
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:741 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

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

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