Variant report

Variant	nsv1000087
Chromosome Location	chr2:50501395-50581229
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	chr2:50575093-50575245	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr2:50573460-50573887	H1-hESC	embryonic stem cell:	n/a	n/a
3	BRCA1	chr2:50575004-50575237	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr2:50574811-50575016	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr2:50538326-50538376	HepG2	liver:	n/a	chr2:50538357-50538368
6	CEBPB	chr2:50501100-50501399	A549	lung:	n/a	n/a
7	CEBPB	chr2:50546541-50546584	K562	blood:	n/a	n/a
8	CEBPB	chr2:50543533-50543755	A549	lung:	n/a	chr2:50543626-50543637 chr2:50543653-50543666 chr2:50543653-50543666
9	CEBPB	chr2:50501078-50501409	IMR90	lung:	n/a	n/a
10	CHD1	chr2:50574393-50575260	H1-hESC	embryonic stem cell:	n/a	chr2:50574651-50574661
11	CHD2	chr2:50574294-50574471	H1-hESC	embryonic stem cell:	n/a	n/a
12	CHD2	chr2:50574674-50575078	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTBP2	chr2:50573194-50575208	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr2:50545400-50545550	HMEC	breast:	n/a	n/a
15	CTCF	chr2:50573389-50573602	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr2:50571715-50572001	MCF-7	breast:	n/a	chr2:50571804-50571820 chr2:50571803-50571821 chr2:50571806-50571819
17	CTCF	chr2:50545431-50545527	LNCaP	prostate:	n/a	n/a
18	CTCF	chr2:50573439-50573539	SK-N-SH_RA	brain:	n/a	n/a
19	CTCF	chr2:50571800-50571950	GM12870	blood:	n/a	chr2:50571804-50571820 chr2:50571803-50571821 chr2:50571806-50571819
20	CTCF	chr2:50553675-50553699	Lung_OC	lung:	n/a	n/a
21	CTCF	chr2:50571680-50571830	GM12875	blood:	n/a	chr2:50571804-50571820 chr2:50571803-50571821 chr2:50571806-50571819
22	CTCF	chr2:50545400-50545550	GM12874	blood:	n/a	n/a
23	CTCF	chr2:50545460-50545610	HMEC	breast:	n/a	n/a
24	CTCF	chr2:50571700-50571850	GM12865	blood:	n/a	chr2:50571804-50571820 chr2:50571803-50571821 chr2:50571806-50571819
25	CTCF	chr2:50571763-50571851	Gliobla	brain:	n/a	chr2:50571804-50571820 chr2:50571803-50571821 chr2:50571806-50571819
26	CTCF	chr2:50545480-50545630	GM12874	blood:	n/a	n/a
27	CTCF	chr2:50545440-50545590	GM12873	blood:	n/a	n/a
28	CTCF	chr2:50571720-50571870	WERI-Rb-1	eye:	n/a	chr2:50571804-50571820 chr2:50571803-50571821 chr2:50571806-50571819
29	CTCF	chr2:50571740-50571890	NHEK	skin:	n/a	chr2:50571804-50571820 chr2:50571803-50571821 chr2:50571806-50571819
30	CTCF	chr2:50571735-50571916	A549	lung:	n/a	chr2:50571804-50571820 chr2:50571803-50571821 chr2:50571806-50571819
31	CTCF	chr2:50571700-50571850	GM12871	blood:	n/a	chr2:50571804-50571820 chr2:50571803-50571821 chr2:50571806-50571819
32	CTCF	chr2:50571808-50571870	Fibrobl	skin:	n/a	n/a
33	CTCF	chr2:50574640-50574790	WERI-Rb-1	eye:	n/a	n/a
34	CTCF	chr2:50545440-50545590	HRPEpiC	eye:	n/a	n/a
35	CTCF	chr2:50571720-50571870	SAEC	small airway:	n/a	chr2:50571804-50571820 chr2:50571803-50571821 chr2:50571806-50571819
36	CTCF	chr2:50571673-50571946	H1-hESC	embryonic stem cell:	n/a	chr2:50571804-50571820 chr2:50571803-50571821 chr2:50571806-50571819
37	CTCF	chr2:50571730-50571930	MCF-7	breast:	n/a	chr2:50571804-50571820 chr2:50571803-50571821 chr2:50571806-50571819
38	CTCF	chr2:50545440-50545590	GM12864	blood:	n/a	n/a
39	CTCF	chr2:50571715-50571903	HepG2	liver:	n/a	chr2:50571804-50571820 chr2:50571803-50571821 chr2:50571806-50571819
40	CTCF	chr2:50545420-50545570	HCT-116	colon:	n/a	n/a
41	CTCF	chr2:50545440-50545590	Caco-2	colon:	n/a	n/a
42	CTCF	chr2:50573780-50573930	SK-N-SH_RA	brain:	n/a	n/a
43	CTCF	chr2:50571700-50571850	K562	blood:	n/a	chr2:50571804-50571820 chr2:50571803-50571821 chr2:50571806-50571819
44	CTCF	chr2:50571720-50571870	HAc	cerebellar:	n/a	chr2:50571804-50571820 chr2:50571803-50571821 chr2:50571806-50571819
45	CTCF	chr2:50571740-50571890	GM12872	blood:	n/a	chr2:50571804-50571820 chr2:50571803-50571821 chr2:50571806-50571819
46	CTCF	chr2:50571720-50571870	GM12864	blood:	n/a	chr2:50571804-50571820 chr2:50571803-50571821 chr2:50571806-50571819
47	CTCF	chr2:50545380-50545530	GM06990	blood:	n/a	n/a
48	CTCF	chr2:50571760-50571910	BE2_C	brain:	n/a	chr2:50571804-50571820 chr2:50571803-50571821 chr2:50571806-50571819
49	CTCF	chr2:50571673-50571882	HepG2	liver:	n/a	chr2:50571804-50571820 chr2:50571803-50571821 chr2:50571806-50571819
50	CTCF	chr2:50571740-50571890	HRPEpiC	eye:	n/a	chr2:50571804-50571820 chr2:50571803-50571821 chr2:50571806-50571819

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:50578420-50578470	PrEC	prostate:	n/a
2	chr2:50570407-50570457	SK-N-SH_RA	brain:	n/a
3	chr2:50574196-50574246	HIPEpiC	eye:	n/a
4	chr2:50574516-50574566	HNPCEpiC	eye:	n/a
5	chr2:50575326-50575376	T-47D	breast:	n/a
6	chr2:50574516-50574566	ProgFib	skin:	n/a
7	chr2:50573485-50573535	AoSMC	blood vessel:	n/a
8	chr2:50575324-50575374	HCT-116	colon:	n/a
9	chr2:50572944-50572994	HAEpiC	amniotic membrane:	n/a
10	chr2:50574516-50574566	HCT-116	colon:	n/a
11	chr2:50578420-50578470	HRPEpiC	eye:	n/a
12	chr2:50574516-50574566	HAEpiC	amniotic membrane:	n/a
13	chr2:50575037-50575087	MCF10A-Er-Src	breast:	n/a
14	chr2:50575030-50575080	K562	blood:	n/a
15	chr2:50575326-50575376	RPTEC	kidney:	n/a
16	chr2:50575093-50575143	Hepatocyte	liver:	n/a
17	chr2:50573485-50573535	Hepatocyte	liver:	n/a
18	chr2:50570407-50570457	NHDF-neo	bronchial:	n/a
19	chr2:50573485-50573535	MCF10A-Er-Src	breast:	n/a
20	chr2:50574912-50574962	NT2-D1	testis:	n/a
21	chr2:50575326-50575376	HRCEpiC	kidney:	n/a
22	chr2:50574912-50574962	U87	brain:	n/a
23	chr2:50570407-50570457	PFSK-1	brain:	n/a
24	chr2:50574516-50574566	HCPEpiC	choroid plexus:	n/a
25	chr2:50574624-50574674	HCM	heart:	n/a
26	chr2:50574912-50574962	HRPEpiC	eye:	n/a
27	chr2:50575069-50575119	BJ	skin:	n/a
28	chr2:50574912-50574962	HCF	heart:	n/a
29	chr2:50574516-50574566	HUVEC	blood vessel:	n/a
30	chr2:50570407-50570457	SK-N-MC	brain:	n/a
31	chr2:50578420-50578470	HCPEpiC	choroid plexus:	n/a
32	chr2:50575030-50575080	ProgFib	skin:	n/a
33	chr2:50578420-50578470	GM12892	blood:	n/a
34	chr2:50575030-50575080	BJ	skin:	n/a
35	chr2:50572944-50572994	HepG2	liver:	n/a
36	chr2:50574708-50574758	HIPEpiC	eye:	n/a
37	chr2:50572944-50572994	GM12891	blood:	n/a
38	chr2:50574516-50574566	ovcar-3	ovarian:	n/a
39	chr2:50575326-50575376	HAEpiC	amniotic membrane:	n/a
40	chr2:50575093-50575143	RPTEC	kidney:	n/a
41	chr2:50574624-50574674	HCF	heart:	n/a
42	chr2:50574708-50574758	HEEpiC	esophagus:	n/a
43	chr2:50575069-50575119	LNCaP	prostate:	n/a
44	chr2:50574708-50574758	ProgFib	skin:	n/a
45	chr2:50572944-50572994	MCF10A-Er-Src	breast:	n/a
46	chr2:50570407-50570457	AG04450	lung:	fetal
47	chr2:50575098-50575148	HEK293	kidney:	embryo
48	chr2:50575093-50575143	HIPEpiC	eye:	n/a
49	chr2:50574624-50574674	AG09309	skin:	n/a
50	chr2:50574912-50574962	ProgFib	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:50523162..50524953-chr4:179777624..179779144,2	MCF-7	breast:
2	chr2:50551521..50552446-chr2:50719322..50720205,2	MCF-7	breast:
3	chr2:50571493..50572317-chr2:50629670..50630519,2	MCF-7	breast:
4	chr2:50571653..50572272-chr2:50719383..50719965,2	MCF-7	breast:

Variant related genes	Relation type
NRXN1	TF binding region
NRXN1	CpG island

Extended variants
information (count: 2555 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:2555 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576716045	chr2:50501403-50501404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs146328692	chr2:50501447-50501448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs559107711	chr2:50501521-50501522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs529806386	chr2:50501524-50501525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs542029570	chr2:50501536-50501537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs561179546	chr2:50501540-50501541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs188789513	chr2:50501569-50501570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs552123375	chr2:50501586-50501587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs386645970	chr2:50501635-50501636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs181206324	chr2:50501669-50501670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs571663058	chr2:50501701-50501702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs532835418	chr2:50501713-50501714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs186167661	chr2:50501720-50501721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs575370570	chr2:50501721-50501722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs536811162	chr2:50501736-50501737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs28375370	chr2:50501740-50501741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs569609641	chr2:50501773-50501774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs537189195	chr2:50501779-50501780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs558263500	chr2:50501789-50501790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs576465292	chr2:50501844-50501845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs564255247	chr2:50501869-50501870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs540643331	chr2:50501907-50501908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs577958946	chr2:50501921-50501922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs144311072	chr2:50501922-50501923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs75860525	chr2:50501931-50501932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs373448169	chr2:50501972-50501973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs540675699	chr2:50502001-50502002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs541622191	chr2:50502024-50502025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs139721152	chr2:50502058-50502059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs576458079	chr2:50502106-50502107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs543926574	chr2:50502141-50502142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs370526444	chr2:50502142-50502143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs75759012	chr2:50502173-50502174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs77632746	chr2:50502212-50502213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs190140417	chr2:50502239-50502240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs560038618	chr2:50502263-50502264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs530432079	chr2:50502267-50502268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs548487848	chr2:50502269-50502270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs371280992	chr2:50502278-50502279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs74854732	chr2:50502299-50502300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs536723907	chr2:50502344-50502345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs10186205	chr2:50502363-50502364	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs182148155	chr2:50502405-50502406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs552558747	chr2:50502457-50502458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs369487350	chr2:50502472-50502473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs141932405	chr2:50502481-50502482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs535791559	chr2:50502511-50502512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs368430237	chr2:50502604-50502605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs575432512	chr2:50502607-50502608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs563078155	chr2:50502639-50502640	Weak transcription	n/a	n/a	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
Bladder cancer	21909424	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
Pancreatic ductal adenocarcinoma	19077451	CNVD
Autism	20531469	CNVD
Autism	20848651	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:381 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:50496400-50519000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr2:50514800-50515200	Enhancers	Pancreatic Islets	Pancreatic Islet
3	chr2:50517800-50518000	Enhancers	Brain Germinal Matrix	brain
4	chr2:50517800-50518200	Enhancers	Fetal Brain Female	brain
5	chr2:50518200-50519400	Weak transcription	Fetal Brain Female	brain
6	chr2:50518400-50519800	Enhancers	Colon Smooth Muscle	Colon
7	chr2:50518600-50518800	Enhancers	Brain Germinal Matrix	brain
8	chr2:50518800-50519200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr2:50519000-50519200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr2:50519600-50519800	Enhancers	Fetal Brain Female	brain
11	chr2:50522400-50524000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr2:50536600-50537000	Enhancers	Fetal Stomach	stomach
13	chr2:50539800-50540400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr2:50540400-50542800	Enhancers	Fetal Brain Female	brain
15	chr2:50540400-50543200	Enhancers	Fetal Brain Male	brain
16	chr2:50540600-50541000	Enhancers	Brain Angular Gyrus	brain
17	chr2:50540600-50543200	Enhancers	Brain Germinal Matrix	brain
18	chr2:50541000-50542400	Weak transcription	Brain Angular Gyrus	brain
19	chr2:50541200-50541400	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr2:50542000-50542600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
21	chr2:50542200-50543400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr2:50542400-50542800	Enhancers	Brain Anterior Caudate	brain
23	chr2:50542400-50543000	Enhancers	Brain Angular Gyrus	brain
24	chr2:50542800-50543600	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr2:50543000-50547800	Weak transcription	Brain Angular Gyrus	brain
26	chr2:50546400-50546800	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr2:50546600-50547000	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr2:50546800-50547000	Enhancers	Fetal Brain Female	brain
29	chr2:50546800-50547200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr2:50546800-50547200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
31	chr2:50547000-50547600	Weak transcription	Fetal Brain Female	brain
32	chr2:50547200-50548200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
33	chr2:50547600-50548400	Enhancers	Fetal Brain Female	brain
34	chr2:50547800-50548400	Enhancers	Brain Angular Gyrus	brain
35	chr2:50548200-50548600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
36	chr2:50548400-50570600	Weak transcription	Brain Angular Gyrus	brain
37	chr2:50558400-50559200	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr2:50558800-50559000	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr2:50558800-50559000	Enhancers	H1 Cell Line	embryonic stem cell
40	chr2:50558800-50559600	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr2:50559000-50560800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
42	chr2:50559000-50562400	Weak transcription	H1 Cell Line	embryonic stem cell
43	chr2:50559200-50559600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
44	chr2:50559600-50559800	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr2:50559600-50561000	Weak transcription	HUES48 Cell Line	embryonic stem cell
46	chr2:50559800-50562000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
47	chr2:50560200-50560400	Enhancers	Fetal Brain Male	brain
48	chr2:50560200-50560600	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr2:50560400-50561400	Weak transcription	Fetal Brain Male	brain
50	chr2:50560600-50560800	Enhancers	H9 Cell Line	embryonic stem cell

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