Variant report

Variant	nsv933174
Chromosome Location	chr2:51203132-51314430
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:349)
CpG islands
(count:1467)
Chromatin interactive
region (count:6)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:349 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr2:51259020-51259511	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr2:51259057-51259636	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr2:51240144-51240458	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr2:51246247-51246255	H1-hESC	embryonic stem cell:	n/a	n/a
5	BRCA1	chr2:51259605-51259656	H1-hESC	embryonic stem cell:	n/a	n/a
6	BRCA1	chr2:51214813-51214934	Hela-S3	cervix:	n/a	n/a
7	CBX3	chr2:51240017-51240569	HCT-116	colon:	n/a	n/a
8	CEBPB	chr2:51229696-51229991	IMR90	lung:	n/a	chr2:51229820-51229831
9	CEBPB	chr2:51256004-51256330	K562	blood:	n/a	chr2:51256172-51256183
10	CEBPB	chr2:51282778-51283040	IMR90	lung:	n/a	chr2:51282886-51282897
11	CEBPB	chr2:51272237-51272566	HepG2	liver:	n/a	chr2:51272397-51272408 chr2:51272396-51272409
12	CEBPB	chr2:51272267-51272564	A549	lung:	n/a	chr2:51272397-51272408 chr2:51272396-51272409
13	CEBPB	chr2:51240147-51240542	MCF-7	breast:	n/a	n/a
14	CEBPB	chr2:51255964-51256336	MCF-7	breast:	n/a	chr2:51256172-51256183
15	CEBPB	chr2:51255984-51256364	HepG2	liver:	n/a	chr2:51256172-51256183
16	CEBPB	chr2:51255989-51256366	IMR90	lung:	n/a	chr2:51256172-51256183
17	CEBPB	chr2:51255980-51256366	H1-hESC	embryonic stem cell:	n/a	chr2:51256172-51256183
18	CEBPB	chr2:51236313-51236416	A549	lung:	n/a	n/a
19	CEBPB	chr2:51256083-51256253	HepG2	liver:	n/a	chr2:51256172-51256183
20	CEBPB	chr2:51229679-51229969	HepG2	liver:	n/a	chr2:51229820-51229831
21	CEBPB	chr2:51256026-51256305	HepG2	liver:	n/a	chr2:51256172-51256183
22	CEBPB	chr2:51229690-51229927	A549	lung:	n/a	chr2:51229820-51229831
23	CEBPB	chr2:51255998-51256347	A549	lung:	n/a	chr2:51256172-51256183
24	CEBPB	chr2:51282756-51283052	HepG2	liver:	n/a	chr2:51282886-51282897
25	CEBPB	chr2:51259207-51259533	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr2:51255896-51256399	A549	lung:	n/a	chr2:51256172-51256183
27	CEBPB	chr2:51256005-51256373	Hela-S3	cervix:	n/a	chr2:51256172-51256183
28	CHD1	chr2:51259142-51259719	IMR90	lung:	n/a	n/a
29	CHD2	chr2:51301746-51301806	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr2:51259157-51260352	H1-hESC	embryonic stem cell:	n/a	n/a
31	CREB1	chr2:51259155-51259702	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTBP2	chr2:51259099-51260033	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr2:51257520-51257670	WERI-Rb-1	eye:	n/a	n/a
34	CTCF	chr2:51278880-51279030	GM12864	blood:	n/a	n/a
35	CTCF	chr2:51223985-51224068	GM20000	blood:	n/a	n/a
36	CTCF	chr2:51257430-51257765	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr2:51257500-51257650	SK-N-SH_RA	brain:	n/a	n/a
38	CTCF	chr2:51230760-51230910	HMEC	breast:	n/a	n/a
39	CTCF	chr2:51300710-51300762	GM10266	blood:	n/a	n/a
40	CTCF	chr2:51312020-51312170	HEEpiC	esophagus:	n/a	n/a
41	CTCF	chr2:51311960-51312110	HMEC	breast:	n/a	n/a
42	CTCF	chr2:51307306-51307343	Lung_OC	lung:	n/a	n/a
43	CTCF	chr2:51257544-51257638	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr2:51312000-51312150	NHEK	skin:	n/a	n/a
45	E2F4	chr2:51247598-51247814	MCF10A-Er-Src	breast:	n/a	n/a
46	E2F4	chr2:51212157-51212179	MCF10A-Er-Src	breast:	n/a	n/a
47	E2F4	chr2:51230837-51231293	MCF10A-Er-Src	breast:	n/a	n/a
48	E2F4	chr2:51309280-51309367	MCF10A-Er-Src	breast:	n/a	n/a
49	E2F4	chr2:51310137-51310570	MCF10A-Er-Src	breast:	n/a	n/a
50	E2F6	chr2:51309441-51310051	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1467 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:51255306-51255356	AG09309	skin:	n/a
2	chr2:51260003-51260053	K562	blood:	n/a
3	chr2:51259807-51259857	HPAEpiC	pulmonary alveolar:	n/a
4	chr2:51255306-51255356	AG09309	skin:	n/a
5	chr2:51260003-51260053	K562	blood:	n/a
6	chr2:51259807-51259857	HPAEpiC	pulmonary alveolar:	n/a
7	chr2:51260739-51260789	HCT-116	colon:	n/a
8	chr2:51255324-51255374	HCF	heart:	n/a
9	chr2:51255306-51255356	AG04450	lung:	fetal
10	chr2:51259552-51259602	PANC-1	pancreas:	n/a
11	chr2:51255324-51255374	K562	blood:	n/a
12	chr2:51255324-51255374	PANC-1	pancreas:	n/a
13	chr2:51228125-51228175	SK-N-SH_RA	brain:	n/a
14	chr2:51260739-51260789	Caco-2	colon:	n/a
15	chr2:51260003-51260053	HRCEpiC	kidney:	n/a
16	chr2:51259786-51259836	H1-hESC	embryonic stem cell:	embryo
17	chr2:51259703-51259753	BJ	skin:	n/a
18	chr2:51231649-51231699	T-47D	breast:	n/a
19	chr2:51254132-51254182	NH-A	brain:	n/a
20	chr2:51255627-51255677	GM19239	blood:	n/a
21	chr2:51254132-51254182	RPTEC	kidney:	n/a
22	chr2:51252301-51252351	HUVEC	blood vessel:	n/a
23	chr2:51259786-51259836	ovcar-3	ovarian:	n/a
24	chr2:51255306-51255356	GM12878	blood:	n/a
25	chr2:51254981-51255031	GM12891	blood:	n/a
26	chr2:51259693-51259743	HCPEpiC	choroid plexus:	n/a
27	chr2:51252301-51252351	MCF-7	breast:	n/a
28	chr2:51254823-51254873	ECC-1	luminal epithelium:	n/a
29	chr2:51260399-51260449	BJ	skin:	n/a
30	chr2:51218880-51218930	AoSMC	blood vessel:	n/a
31	chr2:51252301-51252351	BE2_C	brain:	n/a
32	chr2:51259697-51259747	HEK293	kidney:	embryo
33	chr2:51255627-51255677	HCF	heart:	n/a
34	chr2:51259693-51259743	NHDF-neo	bronchial:	n/a
35	chr2:51260003-51260053	SAEC	small airway:	n/a
36	chr2:51240310-51240360	PFSK-1	brain:	n/a
37	chr2:51254170-51254220	PrEC	prostate:	n/a
38	chr2:51259786-51259836	GM12892	blood:	n/a
39	chr2:51259697-51259747	HIPEpiC	eye:	n/a
40	chr2:51252301-51252351	NB4	blood:	n/a
41	chr2:51259552-51259602	HCM	heart:	n/a
42	chr2:51255306-51255356	GM06990	blood:	n/a
43	chr2:51259786-51259836	SK-N-SH	brain:	n/a
44	chr2:51228125-51228175	AG09319	gingival:	n/a
45	chr2:51254132-51254182	GM12878	blood:	n/a
46	chr2:51260739-51260789	HEK293	kidney:	embryo
47	chr2:51260003-51260053	HepG2	liver:	n/a
48	chr2:51240310-51240360	HRCEpiC	kidney:	n/a
49	chr2:51260003-51260053	HCPEpiC	choroid plexus:	n/a
50	chr2:51240310-51240360	SK-N-MC	brain:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:51313706..51316467-chr2:51317325..51319738,2	K562	blood:
2	chr2:51260931..51263493-chr2:51269854..51271859,2	MCF-7	breast:
3	chr2:51288072..51290967-chr2:232569534..232571521,2	MCF-7	breast:
4	chr2:51281367..51284227-chr2:51284549..51287538,2	K562	blood:
5	chr2:51281367..51284227-chr2:51284549..51287538,2	K562	blood:
6	chr2:51260931..51263493-chr2:51269854..51271859,2	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NRXN1-3	chr2:51283579-51283793	l_1833_chr2:51283578-51306188_testes
2	lnc-NRXN1-3	chr2:51302313-51302437	l_1833_chr2:51283578-51306188_testes
3	lnc-NRXN1-3	chr2:51302314-51302406	NONHSAT070652
4	lnc-NRXN1-3	chr2:51294575-51294743	l_1833_chr2:51283578-51306188_testes
5	lnc-NRXN1-3	chr2:51282723-51282956	NONHSAT070652
6	lnc-NRXN1-3	chr2:51306149-51306209	l_1833_chr2:51283578-51306188_testes
7	lnc-CHAC2-4	chr2:51279495-51279592	ENSG00000231918.1
8	lnc-NRXN1-3	chr2:51283633-51283791	NONHSAT070652
9	lnc-CHAC2-4	chr2:51259739-51260154	ENSG00000231918.1

No data

Variant related genes	Relation type
NRXN1	TF binding region
ENSG00000231918	TF binding region
NRXN1	CpG island
ENSG00000231918	CpG island

Extended variants
information (count: 3455 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:3455 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563640394	chr2:51203144-51203145	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs181894983	chr2:51203172-51203173	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs545832096	chr2:51203176-51203177	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs373213752	chr2:51203188-51203189	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs186236449	chr2:51203194-51203195	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs547393934	chr2:51203197-51203198	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs528607590	chr2:51203213-51203214	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs567180762	chr2:51203255-51203256	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs144637381	chr2:51203309-51203310	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs576892115	chr2:51203333-51203334	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs568130364	chr2:51203341-51203342	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs201032192	chr2:51203348-51203349	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs529095624	chr2:51203400-51203401	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs550847689	chr2:51203427-51203428	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs569222772	chr2:51203464-51203465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs7586490	chr2:51203466-51203467	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs556027202	chr2:51203468-51203469	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs1065244	chr2:51203486-51203487	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs146727347	chr2:51203497-51203498	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs373994310	chr2:51203511-51203512	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs539502208	chr2:51203517-51203518	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs12621330	chr2:51203560-51203561	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs533617344	chr2:51203564-51203565	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs189868286	chr2:51203581-51203582	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs574886156	chr2:51203592-51203593	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs140327852	chr2:51203613-51203614	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs182139200	chr2:51203659-51203660	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs575568631	chr2:51203702-51203703	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs558744706	chr2:51203727-51203728	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs186471759	chr2:51203742-51203743	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs370181344	chr2:51203743-51203744	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs564114800	chr2:51203745-51203746	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs143609780	chr2:51203750-51203751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs371229753	chr2:51203799-51203800	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs540329110	chr2:51203824-51203825	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs562214959	chr2:51203881-51203882	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs375931605	chr2:51203882-51203883	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs572385446	chr2:51203892-51203893	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs191506158	chr2:51203922-51203923	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs550835608	chr2:51203941-51203942	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs569149963	chr2:51203957-51203958	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs533234062	chr2:51203958-51203959	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs66971536	chr2:51204003-51204004	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs566304229	chr2:51204017-51204018	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs533783871	chr2:51204029-51204030	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs555164123	chr2:51204036-51204037	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs182828862	chr2:51204037-51204038	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs561212978	chr2:51204243-51204244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs148068711	chr2:51204282-51204283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs141774899	chr2:51204359-51204360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:97)

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
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
Schizophrenia	20967226	CNVD
Schizophrenia	17989066	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Bipolar disorder	19114987	CNVD
Bladder cancer	21909424	CNVD

Chromatin state (count:713 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:51190400-51221600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr2:51198000-51205600	Weak transcription	Fetal Brain Male	brain
3	chr2:51200200-51203800	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr2:51201200-51204200	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr2:51201200-51205800	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr2:51202000-51203800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr2:51202400-51203200	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr2:51202400-51203400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr2:51202800-51203200	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr2:51202800-51203200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr2:51203800-51204000	Enhancers	H1 Cell Line	embryonic stem cell
12	chr2:51205000-51205400	Enhancers	Fetal Brain Female	brain
13	chr2:51205400-51205800	Weak transcription	Fetal Brain Female	brain
14	chr2:51205600-51205800	Enhancers	Fetal Brain Male	brain
15	chr2:51205600-51207400	Enhancers	Brain Germinal Matrix	brain
16	chr2:51205800-51206400	Weak transcription	Fetal Brain Male	brain
17	chr2:51205800-51206600	Enhancers	Fetal Brain Female	brain
18	chr2:51205800-51207000	Enhancers	Breast Myoepithelial Primary Cells	Breast
19	chr2:51205800-51207200	Enhancers	Pancreatic Islets	Pancreatic Islet
20	chr2:51206000-51206800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr2:51206200-51206600	Enhancers	HMEC	breast
22	chr2:51206400-51206600	Enhancers	Fetal Brain Male	brain
23	chr2:51206600-51208800	Weak transcription	Fetal Brain Male	brain
24	chr2:51207200-51218800	Weak transcription	Pancreatic Islets	Pancreatic Islet
25	chr2:51207400-51237600	Weak transcription	Brain Germinal Matrix	brain
26	chr2:51208800-51209000	Enhancers	Fetal Brain Male	brain
27	chr2:51215200-51215600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr2:51215400-51216000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr2:51215600-51216000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr2:51215800-51216000	Enhancers	Fetal Brain Female	brain
31	chr2:51216000-51216200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr2:51216000-51217800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr2:51216000-51218400	Weak transcription	Fetal Brain Female	brain
34	chr2:51216200-51219800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr2:51217800-51218000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr2:51217800-51218800	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr2:51218000-51218800	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr2:51218400-51218600	Enhancers	Fetal Brain Female	brain
39	chr2:51218400-51218800	Enhancers	Brain Substantia Nigra	brain
40	chr2:51218600-51219400	Weak transcription	Fetal Brain Female	brain
41	chr2:51218800-51219200	Weak transcription	Brain Substantia Nigra	brain
42	chr2:51218800-51222200	Enhancers	Pancreatic Islets	Pancreatic Islet
43	chr2:51218800-51225600	Weak transcription	HUES48 Cell Line	embryonic stem cell
44	chr2:51218800-51226400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
45	chr2:51219200-51219400	Enhancers	Brain Substantia Nigra	brain
46	chr2:51219400-51220200	Enhancers	Fetal Brain Female	brain
47	chr2:51219400-51227200	Weak transcription	Brain Substantia Nigra	brain
48	chr2:51219600-51220000	Enhancers	Fetal Brain Male	brain
49	chr2:51219800-51222400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr2:51220200-51227200	Weak transcription	Fetal Brain Female	brain

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