Variant report

Variant	nsv933691
Chromosome Location	chr2:50908459-51009190
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	chr2:50952000-50952353	HepG2	liver:	n/a	n/a
3	CEBPB	chr2:50951993-50952357	IMR90	lung:	n/a	n/a
4	CEBPB	chr2:50919241-50919557	IMR90	lung:	n/a	chr2:50919400-50919413 chr2:50919400-50919411
5	CEBPB	chr2:50919262-50919518	K562	blood:	n/a	chr2:50919400-50919413 chr2:50919400-50919411
6	CEBPB	chr2:50952033-50952347	A549	lung:	n/a	n/a
7	CEBPB	chr2:50954382-50954517	HepG2	liver:	n/a	n/a
8	CEBPB	chr2:50952036-50952291	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr2:50951301-50951586	HepG2	liver:	n/a	chr2:50951423-50951436 chr2:50951424-50951435
10	CEBPB	chr2:50919242-50919552	HepG2	liver:	n/a	chr2:50919400-50919413 chr2:50919400-50919411
11	CEBPB	chr2:51003545-51003679	IMR90	lung:	n/a	n/a
12	CEBPB	chr2:50974968-50975018	HepG2	liver:	n/a	n/a
13	CHD2	chr2:50947884-50948198	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr2:50973654-50974028	GM12878	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
15	CTCF	chr2:50973705-50973915	A549	lung:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
16	CTCF	chr2:50973620-50973770	A549	lung:	n/a	n/a
17	CTCF	chr2:50973740-50973890	GM12867	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
18	CTCF	chr2:50973740-50973890	HepG2	liver:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
19	CTCF	chr2:50973780-50973930	HRPEpiC	eye:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
20	CTCF	chr2:50973572-50973669	Gliobla	brain:	n/a	n/a
21	CTCF	chr2:50973773-50973916	MCF-7	breast:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
22	CTCF	chr2:50973800-50973950	GM12864	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
23	CTCF	chr2:50973760-50973910	Hela-S3	cervix:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
24	CTCF	chr2:50973720-50973870	HFF-Myc	foreskin:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
25	CTCF	chr2:50973772-50973922	GM19239	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
26	CTCF	chr2:50973743-50973945	Pancreas_OC	pancreas:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
27	CTCF	chr2:50973780-50973930	SK-N-SH_RA	brain:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
28	CTCF	chr2:50973720-50973870	HVMF	connective:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
29	CTCF	chr2:50973780-50973930	AG04450	lung:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
30	CTCF	chr2:50973800-50973950	GM12874	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
31	CTCF	chr2:50973740-50973890	AG10803	skin:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
32	CTCF	chr2:50973740-50973890	HRE	kidney:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
33	CTCF	chr2:50973740-50973890	HEEpiC	esophagus:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
34	CTCF	chr2:50973729-50973949	NHEK	skin:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
35	CTCF	chr2:50973732-50973938	MCF-7	breast:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
36	CTCF	chr2:50973780-50973930	BE2_C	brain:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
37	CTCF	chr2:50973760-50973910	AG04450	lung:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
38	CTCF	chr2:50973760-50973910	WI-38	lung:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
39	CTCF	chr2:50976420-50976570	Caco-2	colon:	n/a	n/a
40	CTCF	chr2:50973820-50973970	HEEpiC	esophagus:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
41	CTCF	chr2:50973740-50973890	HAc	cerebellar:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
42	CTCF	chr2:50973760-50973910	HPAF	blood vessel:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
43	CTCF	chr2:50973740-50973890	GM12870	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
44	CTCF	chr2:50973747-50973915	A549	lung:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
45	CTCF	chr2:50973800-50973950	HAc	cerebellar:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
46	CTCF	chr2:50973760-50973910	BE2_C	brain:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
47	CTCF	chr2:50973740-50973890	AoAF	blood vessel:	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	chr2:50973705-50973962	Hela-S3	cervix:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
50	CTCF	chr2:50973780-50973930	HCPEpiC	choroid plexus:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:51001003-51001053	PANC-1	pancreas:	n/a
2	chr2:50956659-50956709	MCF-7	breast:	n/a
3	chr2:51001003-51001053	HL-60	blood:	n/a
4	chr2:50956659-50956709	HCPEpiC	choroid plexus:	n/a
5	chr2:51001003-51001053	HepG2	liver:	n/a
6	chr2:50992829-50992879	BJ	skin:	n/a
7	chr2:51001003-51001053	HPAEpiC	pulmonary alveolar:	n/a
8	chr2:50992829-50992879	HRPEpiC	eye:	n/a
9	chr2:50992829-50992879	MCF-7	breast:	n/a
10	chr2:50956659-50956709	SK-N-SH_RA	brain:	n/a
11	chr2:50992829-50992879	Hela-S3	cervix:	n/a
12	chr2:50956659-50956709	GM19239	blood:	n/a
13	chr2:50956659-50956709	GM12891	blood:	n/a
14	chr2:51001003-51001053	NHBE	bronchial:	n/a
15	chr2:50956659-50956709	A549	lung:	n/a
16	chr2:51001003-51001053	NT2-D1	testis:	n/a
17	chr2:50956659-50956709	AG04449	skin:	fetal
18	chr2:50956659-50956709	NB4	blood:	n/a
19	chr2:50956659-50956709	PrEC	prostate:	n/a
20	chr2:50992829-50992879	HAEpiC	amniotic membrane:	n/a
21	chr2:50992829-50992879	AG04449	skin:	fetal
22	chr2:51001003-51001053	PFSK-1	brain:	n/a
23	chr2:51001003-51001053	LNCaP	prostate:	n/a
24	chr2:50956659-50956709	SK-N-MC	brain:	n/a
25	chr2:50992829-50992879	HUVEC	blood vessel:	n/a
26	chr2:50956659-50956709	BJ	skin:	n/a
27	chr2:50992829-50992879	U87	brain:	n/a
28	chr2:50956659-50956709	HEK293	kidney:	embryo
29	chr2:50992829-50992879	HRCEpiC	kidney:	n/a
30	chr2:50956659-50956709	HCT-116	colon:	n/a
31	chr2:51001003-51001053	HCM	heart:	n/a
32	chr2:50992829-50992879	Jurkat	blood:	n/a
33	chr2:50992829-50992879	SAEC	small airway:	n/a
34	chr2:50992829-50992879	HCT-116	colon:	n/a
35	chr2:51001003-51001053	HEEpiC	esophagus:	n/a
36	chr2:51001003-51001053	ProgFib	skin:	n/a
37	chr2:50992829-50992879	HCF	heart:	n/a
38	chr2:50956659-50956709	Jurkat	blood:	n/a
39	chr2:50956659-50956709	NHBE	bronchial:	n/a
40	chr2:50992829-50992879	PANC-1	pancreas:	n/a
41	chr2:51001003-51001053	SK-N-MC	brain:	n/a
42	chr2:51001003-51001053	AoSMC	blood vessel:	n/a
43	chr2:51001003-51001053	HMEC	breast:	n/a
44	chr2:50956659-50956709	HRPEpiC	eye:	n/a
45	chr2:50956659-50956709	PANC-1	pancreas:	n/a
46	chr2:51001003-51001053	AG09309	skin:	n/a
47	chr2:50992829-50992879	K562	blood:	n/a
48	chr2:50992829-50992879	AG09309	skin:	n/a
49	chr2:51001003-51001053	IMR90	lung:	fetal
50	chr2:50956659-50956709	NH-A	brain:	n/a

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

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

Extended variants
information (count: 3597 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:3597 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

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: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:495 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

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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