Variant report

Variant	nsv533791
Chromosome Location	chr2:50850691-50982113
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	chr2:50951993-50952357	IMR90	lung:	n/a	n/a
3	CEBPB	chr2:50952033-50952347	A549	lung:	n/a	n/a
4	CEBPB	chr2:50952036-50952291	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr2:50954382-50954517	HepG2	liver:	n/a	n/a
6	CEBPB	chr2:50952000-50952353	HepG2	liver:	n/a	n/a
7	CEBPB	chr2:50974968-50975018	HepG2	liver:	n/a	n/a
8	CEBPB	chr2:50854171-50854480	A549	lung:	n/a	chr2:50854319-50854330 chr2:50854320-50854331 chr2:50854319-50854332
9	CEBPB	chr2:50919262-50919518	K562	blood:	n/a	chr2:50919400-50919413 chr2:50919400-50919411
10	CEBPB	chr2:50890728-50891191	HepG2	liver:	n/a	chr2:50890749-50890760 chr2:50891044-50891055
11	CEBPB	chr2:50854196-50854476	IMR90	lung:	n/a	chr2:50854319-50854330 chr2:50854320-50854331 chr2:50854319-50854332
12	CEBPB	chr2:50919242-50919552	HepG2	liver:	n/a	chr2:50919400-50919413 chr2:50919400-50919411
13	CEBPB	chr2:50854209-50854495	HepG2	liver:	n/a	chr2:50854319-50854330 chr2:50854320-50854331 chr2:50854319-50854332
14	CEBPB	chr2:50951301-50951586	HepG2	liver:	n/a	chr2:50951423-50951436 chr2:50951424-50951435
15	CEBPB	chr2:50858684-50858994	HepG2	liver:	n/a	chr2:50858808-50858817 chr2:50858807-50858818 chr2:50858808-50858817 chr2:50858808-50858817 chr2:50858806-50858817 chr2:50858808-50858817
16	CEBPB	chr2:50919241-50919557	IMR90	lung:	n/a	chr2:50919400-50919413 chr2:50919400-50919411
17	CHD2	chr2:50947884-50948198	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr2:50902100-50902250	BE2_C	brain:	n/a	n/a
19	CTCF	chr2:50973780-50973930	SK-N-SH_RA	brain:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
20	CTCF	chr2:50973740-50973890	HRE	kidney:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
21	CTCF	chr2:50902139-50902314	GM12891	blood:	n/a	n/a
22	CTCF	chr2:50902140-50902290	GM06990	blood:	n/a	n/a
23	CTCF	chr2:50973751-50973938	GM12892	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
24	CTCF	chr2:50902100-50902250	HCT-116	colon:	n/a	n/a
25	CTCF	chr2:50973760-50973910	RPTEC	kidney:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
26	CTCF	chr2:50902100-50902250	WERI-Rb-1	eye:	n/a	n/a
27	CTCF	chr2:50973740-50973890	HAc	cerebellar:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
28	CTCF	chr2:50902100-50902250	GM12870	blood:	n/a	n/a
29	CTCF	chr2:50902120-50902270	Hela-S3	cervix:	n/a	n/a
30	CTCF	chr2:50973780-50973930	GM12865	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
31	CTCF	chr2:50973731-50973929	LNCaP	prostate:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
32	CTCF	chr2:50902140-50902290	HMEC	breast:	n/a	n/a
33	CTCF	chr2:50973760-50973910	HA-sp	spinal cord:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
34	CTCF	chr2:50973780-50973930	GM12875	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
35	CTCF	chr2:50973554-50974218	SK-N-SH	brain:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
36	CTCF	chr2:50902116-50902324	GM12892	blood:	n/a	n/a
37	CTCF	chr2:50973720-50973870	HPF	lung:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
38	CTCF	chr2:50973721-50973966	HepG2	liver:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
39	CTCF	chr2:50973800-50973950	MCF-7	breast:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
40	CTCF	chr2:50973752-50973913	GM10248	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
41	CTCF	chr2:50973760-50973910	GM12875	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
42	CTCF	chr2:50889585-50889672	MCF-7	breast:	n/a	n/a
43	CTCF	chr2:50973620-50973770	A549	lung:	n/a	n/a
44	CTCF	chr2:50973760-50973910	GM12871	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
45	CTCF	chr2:50973780-50973930	GM12874	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
46	CTCF	chr2:50973739-50973958	LNCaP	prostate:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
47	CTCF	chr2:50902100-50902250	NHEK	skin:	n/a	n/a
48	CTCF	chr2:50973740-50973890	GM12871	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
49	CTCF	chr2:50973820-50973970	HFF-Myc	foreskin:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
50	CTCF	chr2:50902100-50902250	HMF	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:50956659-50956709	HL-60	blood:	n/a
2	chr2:50884693-50884743	GM12878	blood:	n/a
3	chr2:50884252-50884302	SK-N-SH_RA	brain:	n/a
4	chr2:50863603-50863653	RPTEC	kidney:	n/a
5	chr2:50884693-50884743	RPTEC	kidney:	n/a
6	chr2:50884693-50884743	HEEpiC	esophagus:	n/a
7	chr2:50863603-50863653	HCF	heart:	n/a
8	chr2:50884252-50884302	Hepatocyte	liver:	n/a
9	chr2:50956659-50956709	HRPEpiC	eye:	n/a
10	chr2:50863603-50863653	PrEC	prostate:	n/a
11	chr2:50863603-50863653	BE2_C	brain:	n/a
12	chr2:50863603-50863653	HNPCEpiC	eye:	n/a
13	chr2:50884693-50884743	AG04450	lung:	fetal
14	chr2:50863603-50863653	NHDF-neo	bronchial:	n/a
15	chr2:50956659-50956709	LNCaP	prostate:	n/a
16	chr2:50876837-50876887	GM12891	blood:	n/a
17	chr2:50876837-50876887	SAEC	small airway:	n/a
18	chr2:50852209-50852259	PFSK-1	brain:	n/a
19	chr2:50876837-50876887	NHBE	bronchial:	n/a
20	chr2:50863603-50863653	HIPEpiC	eye:	n/a
21	chr2:50884693-50884743	Hepatocyte	liver:	n/a
22	chr2:50852209-50852259	SK-N-SH_RA	brain:	n/a
23	chr2:50884252-50884302	AG09309	skin:	n/a
24	chr2:50884693-50884743	ProgFib	skin:	n/a
25	chr2:50852209-50852259	K562	blood:	n/a
26	chr2:50884252-50884302	HNPCEpiC	eye:	n/a
27	chr2:50863603-50863653	CMK	blood:	n/a
28	chr2:50884252-50884302	MCF10A-Er-Src	breast:	n/a
29	chr2:50956659-50956709	NB4	blood:	n/a
30	chr2:50956659-50956709	RPTEC	kidney:	n/a
31	chr2:50876837-50876887	HCPEpiC	choroid plexus:	n/a
32	chr2:50884252-50884302	HRPEpiC	eye:	n/a
33	chr2:50852209-50852259	HCM	heart:	n/a
34	chr2:50863603-50863653	HUVEC	blood vessel:	n/a
35	chr2:50884693-50884743	HRE	kidney:	n/a
36	chr2:50876837-50876887	AG09319	gingival:	n/a
37	chr2:50884693-50884743	K562	blood:	n/a
38	chr2:50884693-50884743	HEK293	kidney:	embryo
39	chr2:50852209-50852259	HRCEpiC	kidney:	n/a
40	chr2:50852209-50852259	AG09309	skin:	n/a
41	chr2:50884252-50884302	GM06990	blood:	n/a
42	chr2:50884693-50884743	MCF-7	breast:	n/a
43	chr2:50852209-50852259	HL-60	blood:	n/a
44	chr2:50876837-50876887	HNPCEpiC	eye:	n/a
45	chr2:50852209-50852259	CMK	blood:	n/a
46	chr2:50884693-50884743	PFSK-1	brain:	n/a
47	chr2:50884252-50884302	NHBE	bronchial:	n/a
48	chr2:50863603-50863653	SKMC	muscle:	n/a
49	chr2:50884252-50884302	Caco-2	colon:	n/a
50	chr2:50863603-50863653	NHBE	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:50884111..50885778-chr2:50886770..50888521,2	MCF-7	breast:
2	chr2:50965713..50967269-chr2:50975937..50978033,2	K562	blood:
3	chr2:50977335..50979735-chr2:50992909..50995322,2	K562	blood:
4	chr2:50884335..50886694-chr2:50887318..50889235,3	K562	blood:
5	chr2:50946676..50947176-chr20:60981159..60981778,2	MCF-7	breast:
6	chr2:50884111..50885778-chr2:50886770..50888521,2	MCF-7	breast:
7	chr2:50965713..50967269-chr2:50975937..50978033,2	K562	blood:
8	chr2:50884335..50886694-chr2:50887318..50889235,3	K562	blood:
9	chr2:50973459..50974271-chr2:52224493..52225477,4	MCF-7	breast:
10	chr2:50883231..50884999-chr2:50887642..50889397,2	MCF-7	breast:
11	chr2:50909775..50912434-chr2:50920496..50923402,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-STON1-GTF2A1L-4	chr2:50851950-50852041	NONHSAT070645
2	lnc-STON1-GTF2A1L-4	chr2:50859486-50859749	NONHSAT070645
3	lnc-STON1-GTF2A1L-4	chr2:50858415-50858521	NONHSAT070645

Variant related genes	Relation type
ENSG00000216191	TF binding region
NRXN1	TF binding region
ENSG00000216191	CpG island
NRXN1	CpG island
ENSG00000179915	chromatin interactions
ENSG00000216191	chromatin interactions

Extended variants
information (count: 4676 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:4676 , 50 per page) page: 1 2 3 4 5 6 7 ... 94

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs200464704	chr2:50850704-50850705	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs373654735	chr2:50850722-50850723	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs201753471	chr2:50850731-50850732	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs199712573	chr2:50850758-50850759	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs200537932	chr2:50850761-50850762	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs201902998	chr2:50850774-50850775	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs370497222	chr2:50850779-50850780	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs558908577	chr2:50850793-50850794	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs149840385	chr2:50850794-50850795	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs200151215	chr2:50850799-50850800	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs541733372	chr2:50850811-50850812	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs560055109	chr2:50850813-50850814	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs145859715	chr2:50850827-50850828	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs555460002	chr2:50850840-50850841	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs7606886	chr2:50850846-50850847	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs563246474	chr2:50850908-50850909	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs530617101	chr2:50850920-50850921	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs551930092	chr2:50850921-50850922	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs78879318	chr2:50850926-50850927	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs528404021	chr2:50850927-50850928	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs35218961	chr2:50850930-50850931	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs149044987	chr2:50850951-50850952	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs145743059	chr2:50850986-50850987	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs567984736	chr2:50851030-50851031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs112791872	chr2:50851034-50851035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs181876763	chr2:50851047-50851048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs77219550	chr2:50851065-50851066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs570096816	chr2:50851114-50851115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs533522263	chr2:50851148-50851149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs186087188	chr2:50851161-50851162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs540818137	chr2:50851177-50851178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs558718926	chr2:50851190-50851191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs112224903	chr2:50851194-50851195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs534989891	chr2:50851205-50851206	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs373430081	chr2:50851213-50851214	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs189809186	chr2:50851220-50851221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs180958629	chr2:50851231-50851232	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs542479272	chr2:50851246-50851247	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs201244381	chr2:50851297-50851298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs141193945	chr2:50851306-50851307	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs575271900	chr2:50851330-50851331	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs545867618	chr2:50851334-50851335	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs563990935	chr2:50851376-50851377	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs528096164	chr2:50851394-50851395	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs146984557	chr2:50851434-50851435	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs186029214	chr2:50851456-50851457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs544171210	chr2:50851486-50851487	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs529537805	chr2:50851504-50851505	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs191354402	chr2:50851527-50851528	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs201066469	chr2:50851548-50851549	Weak transcription Enhancers	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:512 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:50839000-50851800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr2:50843000-50853600	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr2:50848200-50851800	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr2:50849400-50854600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr2:50850200-50850800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr2:50850200-50850800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr2:50850400-50850800	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr2:50850400-50850800	Enhancers	H1 Cell Line	embryonic stem cell
9	chr2:50850600-50850800	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr2:50850600-50851600	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr2:50850600-50852600	Weak transcription	Brain Germinal Matrix	brain
12	chr2:50850800-50851200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr2:50850800-50851800	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr2:50850800-50854800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
15	chr2:50851200-50852400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr2:50851600-50852000	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr2:50851800-50852000	Enhancers	H1 Cell Line	embryonic stem cell
18	chr2:50851800-50852000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
19	chr2:50851800-50852400	Enhancers	Cortex derived primary cultured neurospheres	brain
20	chr2:50852000-50854400	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr2:50854400-50855200	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr2:50854600-50854800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr2:50854800-50855000	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr2:50854800-50855200	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr2:50854800-50860200	Weak transcription	Fetal Brain Male	brain
26	chr2:50855200-50862600	Weak transcription	HUES48 Cell Line	embryonic stem cell
27	chr2:50860200-50860400	Enhancers	Fetal Brain Male	brain
28	chr2:50862000-50863600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr2:50862000-50863800	Enhancers	H1 Cell Line	embryonic stem cell
30	chr2:50862000-50864600	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr2:50862600-50863600	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr2:50862600-50864000	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr2:50862600-50865800	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr2:50862800-50863800	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr2:50862800-50865800	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr2:50863000-50864200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
37	chr2:50863000-50864800	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr2:50863400-50863800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr2:50863400-50864000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr2:50863400-50864000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr2:50863600-50864000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
42	chr2:50863800-50865400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
43	chr2:50864000-50864600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
44	chr2:50864000-50865600	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr2:50864600-50864800	Enhancers	iPS-20b Cell Line	embryonic stem cell
46	chr2:50864600-50866200	Weak transcription	HUES6 Cell Line	embryonic stem cell
47	chr2:50865600-50865800	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr2:50866200-50866400	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr2:50868400-50868600	Enhancers	Fetal Brain Male	brain
50	chr2:50868600-50869000	Enhancers	Fetal Muscle Leg	muscle

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