Variant report

Variant	nsv933632
Chromosome Location	chr2:50958645-51079286
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	CEBPB	chr2:51077732-51078049	Hela-S3	cervix:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
2	CEBPB	chr2:50974968-50975018	HepG2	liver:	n/a	n/a
3	CEBPB	chr2:51042082-51042350	A549	lung:	n/a	chr2:51042175-51042186
4	CEBPB	chr2:51077720-51078095	HepG2	liver:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
5	CEBPB	chr2:51051532-51051664	HepG2	liver:	n/a	chr2:51051618-51051629 chr2:51051616-51051627 chr2:51051616-51051629
6	CEBPB	chr2:51077765-51078077	A549	lung:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
7	CEBPB	chr2:51077727-51078088	H1-hESC	embryonic stem cell:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
8	CEBPB	chr2:51039958-51040191	HepG2	liver:	n/a	n/a
9	CEBPB	chr2:51003545-51003679	IMR90	lung:	n/a	n/a
10	CEBPB	chr2:51068879-51068992	HepG2	liver:	n/a	chr2:51068958-51068969
11	CEBPB	chr2:51042035-51042364	HepG2	liver:	n/a	chr2:51042175-51042186
12	CEBPB	chr2:51077746-51078099	IMR90	lung:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
13	CHD2	chr2:51020103-51020131	GM12878	blood:	n/a	n/a
14	CTCF	chr2:50973800-50973950	GM12870	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
15	CTCF	chr2:50973820-50973970	K562	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
16	CTCF	chr2:50973760-50973910	HCPEpiC	choroid plexus:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
17	CTCF	chr2:50973420-50973570	HCM	heart:	n/a	n/a
18	CTCF	chr2:50973780-50973930	HCT-116	colon:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
19	CTCF	chr2:50973740-50973890	AG09319	gingival:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
20	CTCF	chr2:50973687-50973983	Gliobla	brain:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
21	CTCF	chr2:50969658-50969686	MCF-7	breast:	n/a	n/a
22	CTCF	chr2:50973760-50973910	GM12872	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
23	CTCF	chr2:50973760-50973910	HCT-116	colon:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
24	CTCF	chr2:50973747-50973915	A549	lung:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
25	CTCF	chr2:50973704-50973959	H1-hESC	embryonic stem cell:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
26	CTCF	chr2:50973760-50973910	K562	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
27	CTCF	chr2:50973625-50974108	A549	lung:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
28	CTCF	chr2:50973752-50973928	H1-hESC	embryonic stem cell:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
29	CTCF	chr2:50973795-50973920	Spleen_OC	spleen:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
30	CTCF	chr2:50973720-50973870	HPF	lung:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
31	CTCF	chr2:50973740-50973890	SAEC	small airway:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
32	CTCF	chr2:50978500-50978650	HMEC	breast:	n/a	n/a
33	CTCF	chr2:50973746-50973953	A549	lung:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
34	CTCF	chr2:50973760-50973910	AG04449	skin:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
35	CTCF	chr2:50973780-50973930	HMEC	breast:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
36	CTCF	chr2:50973752-50973932	GM12891	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
37	CTCF	chr2:50973760-50973910	GM06990	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
38	CTCF	chr2:50973634-50974016	HCT-116	colon:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
39	CTCF	chr2:51013620-51013770	SK-N-SH_RA	brain:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
40	CTCF	chr2:50973746-50973940	MCF-7	breast:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
41	CTCF	chr2:50973780-50973930	AG04449	skin:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
42	CTCF	chr2:50973780-50973930	HCPEpiC	choroid plexus:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
43	CTCF	chr2:50973780-50973930	HepG2	liver:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
44	CTCF	chr2:50973740-50973890	HFF	foreskin:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
45	CTCF	chr2:50976420-50976570	Caco-2	colon:	n/a	n/a
46	CTCF	chr2:50973641-50974055	H1-hESC	embryonic stem cell:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
47	CTCF	chr2:50973728-50973980	HepG2	liver:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
48	CTCF	chr2:50973760-50973910	HPAF	blood vessel:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
49	CTCF	chr2:50973760-50973910	GM12875	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
50	CTCF	chr2:50973722-50973924	SK-N-SH_RA	brain:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:51074881-51074931	ECC-1	luminal epithelium:	n/a
2	chr2:51057548-51057598	HNPCEpiC	eye:	n/a
3	chr2:51074881-51074931	ECC-1	luminal epithelium:	n/a
4	chr2:51057548-51057598	HNPCEpiC	eye:	n/a
5	chr2:51065673-51065723	HCM	heart:	n/a
6	chr2:51057218-51057268	CMK	blood:	n/a
7	chr2:51056822-51056872	PFSK-1	brain:	n/a
8	chr2:51056884-51056934	MCF-7	breast:	n/a
9	chr2:51074881-51074931	MCF10A-Er-Src	breast:	n/a
10	chr2:51074881-51074931	MCF-7	breast:	n/a
11	chr2:51057218-51057268	SK-N-SH	brain:	n/a
12	chr2:50992829-50992879	NHDF-neo	bronchial:	n/a
13	chr2:51057548-51057598	NT2-D1	testis:	n/a
14	chr2:50992829-50992879	U87	brain:	n/a
15	chr2:51056884-51056934	ECC-1	luminal epithelium:	n/a
16	chr2:51056884-51056934	RPTEC	kidney:	n/a
17	chr2:51056822-51056872	NB4	blood:	n/a
18	chr2:51056884-51056934	HRE	kidney:	n/a
19	chr2:51074939-51074989	HRPEpiC	eye:	n/a
20	chr2:51065673-51065723	LNCaP	prostate:	n/a
21	chr2:51056884-51056934	HepG2	liver:	n/a
22	chr2:51056822-51056872	ovcar-3	ovarian:	n/a
23	chr2:51056822-51056872	BJ	skin:	n/a
24	chr2:50992829-50992879	T-47D	breast:	n/a
25	chr2:51065673-51065723	HPAEpiC	pulmonary alveolar:	n/a
26	chr2:51001003-51001053	SAEC	small airway:	n/a
27	chr2:51057218-51057268	ProgFib	skin:	n/a
28	chr2:51065673-51065723	NHBE	bronchial:	n/a
29	chr2:51065673-51065723	MCF10A-Er-Src	breast:	n/a
30	chr2:51056822-51056872	MCF-7	breast:	n/a
31	chr2:51001003-51001053	Caco-2	colon:	n/a
32	chr2:51065673-51065723	SAEC	small airway:	n/a
33	chr2:51057548-51057598	BE2_C	brain:	n/a
34	chr2:51074939-51074989	K562	blood:	n/a
35	chr2:51056884-51056934	Caco-2	colon:	n/a
36	chr2:51065673-51065723	NH-A	brain:	n/a
37	chr2:51074939-51074989	GM12878	blood:	n/a
38	chr2:51074881-51074931	SAEC	small airway:	n/a
39	chr2:51074881-51074931	NT2-D1	testis:	n/a
40	chr2:50992829-50992879	MCF10A-Er-Src	breast:	n/a
41	chr2:50992829-50992879	NH-A	brain:	n/a
42	chr2:51065673-51065723	HAEpiC	amniotic membrane:	n/a
43	chr2:51074939-51074989	HEEpiC	esophagus:	n/a
44	chr2:51056822-51056872	HUVEC	blood vessel:	n/a
45	chr2:50992829-50992879	HNPCEpiC	eye:	n/a
46	chr2:51056884-51056934	HNPCEpiC	eye:	n/a
47	chr2:51056822-51056872	SAEC	small airway:	n/a
48	chr2:51057218-51057268	H1-hESC	embryonic stem cell:	embryo
49	chr2:51057548-51057598	AG09309	skin:	n/a
50	chr2:51057548-51057598	SAEC	small airway:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:50973459..50974271-chr2:52224493..52225477,4	MCF-7	breast:
2	chr2:50965713..50967269-chr2:50975937..50978033,2	K562	blood:
3	chr2:51018306..51019906-chr2:51022210..51025087,2	K562	blood:
4	chr2:50977335..50979735-chr2:50992909..50995322,2	K562	blood:
5	chr2:50965713..50967269-chr2:50975937..50978033,2	K562	blood:
6	chr2:50985182..50988156-chr2:50995412..50998213,2	K562	blood:
7	chr2:51018306..51019906-chr2:51022210..51025087,2	K562	blood:
8	chr2:50977335..50979735-chr2:50992909..50995322,2	K562	blood:
9	chr2:50985182..50988156-chr2:50995412..50998213,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FSHR-5	chr2:51056580-51056816	NONHSAT070648

Variant related genes	Relation type
ENSG00000238165	TF binding region
ENSG00000215968	TF binding region
ENSG00000238165	CpG island
ENSG00000215968	CpG island

Extended variants
information (count: 4142 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:4142 , 50 per page) page: 1 2 3 4 5 6 7 ... 83

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs377621629	chr2:50958653-50958654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs543926525	chr2:50958694-50958695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs369966712	chr2:50958706-50958707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs577209409	chr2:50958728-50958729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs541064828	chr2:50958756-50958757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs559738450	chr2:50958779-50958780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs530427191	chr2:50958780-50958781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs858950	chr2:50958782-50958783	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs114045089	chr2:50958818-50958819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs530995758	chr2:50958828-50958829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs552287406	chr2:50958846-50958847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs149261338	chr2:50958894-50958895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs192473124	chr2:50958940-50958941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs562621173	chr2:50959013-50959014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs542532579	chr2:50959031-50959032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs144490712	chr2:50959108-50959109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs546195146	chr2:50959158-50959159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs184482401	chr2:50959187-50959188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs535385789	chr2:50959210-50959211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs556817285	chr2:50959220-50959221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs35408355	chr2:50959295-50959296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs531821816	chr2:50959313-50959314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs551526775	chr2:50959323-50959324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs539247738	chr2:50959354-50959355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs559057291	chr2:50959413-50959414	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs577269969	chr2:50959507-50959508	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs541476354	chr2:50959535-50959536	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs370370587	chr2:50959536-50959537	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs559805801	chr2:50959544-50959545	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs574863064	chr2:50959578-50959579	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs556472275	chr2:50959613-50959614	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs542574494	chr2:50959647-50959648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs563961996	chr2:50959660-50959661	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs116951553	chr2:50959670-50959671	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs858951	chr2:50959683-50959684	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs148046555	chr2:50959700-50959701	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs189006337	chr2:50959758-50959759	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs377143109	chr2:50959778-50959779	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs192941611	chr2:50959802-50959803	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs184633046	chr2:50959903-50959904	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs535069732	chr2:50959905-50959906	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs550504007	chr2:50959921-50959922	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs569055070	chr2:50959929-50959930	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs527938048	chr2:50960001-50960002	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs539672769	chr2:50960021-50960022	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs35541167	chr2:50960025-50960026	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs141724178	chr2:50960085-50960086	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs566391032	chr2:50960088-50960089	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs115798270	chr2:50960118-50960119	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs553487426	chr2:50960256-50960257	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
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
Autism	20841430	CNVD
Schizophrenia	20967226	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:50951200-50959800	Weak transcription	Brain Anterior Caudate	brain
2	chr2:50955600-50959800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr2:50956200-50959400	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr2:50959400-50960000	Enhancers	Pancreatic Islets	Pancreatic Islet
5	chr2:50959800-50960000	Enhancers	Brain Anterior Caudate	brain
6	chr2:50959800-50960200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr2:50960000-50961600	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chr2:50961600-50961800	Enhancers	Pancreatic Islets	Pancreatic Islet
9	chr2:50965400-50966200	Enhancers	Brain Germinal Matrix	brain
10	chr2:50966200-50967800	Weak transcription	Brain Germinal Matrix	brain
11	chr2:50967800-50968400	Enhancers	Brain Germinal Matrix	brain
12	chr2:50971800-50972200	Enhancers	Pancreatic Islets	Pancreatic Islet
13	chr2:50972200-50975800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr2:50972200-50978200	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr2:50974200-50974400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr2:50974200-50974400	Weak transcription	Brain Germinal Matrix	brain
17	chr2:50974400-50974600	Enhancers	Brain Hippocampus Middle	brain
18	chr2:50974400-50975200	Enhancers	HSMMtube	muscle
19	chr2:50974400-50976200	Enhancers	Brain Germinal Matrix	brain
20	chr2:50974400-50978200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr2:50975000-50976000	Enhancers	Fetal Muscle Leg	muscle
22	chr2:50975000-50976800	Enhancers	Fetal Brain Female	brain
23	chr2:50975200-50975800	Enhancers	Fetal Brain Male	brain
24	chr2:50975200-50977200	Enhancers	Cortex derived primary cultured neurospheres	brain
25	chr2:50975400-50975600	Enhancers	Brain Inferior Temporal Lobe	brain
26	chr2:50975400-50975800	Enhancers	Brain Hippocampus Middle	brain
27	chr2:50975600-50975800	Enhancers	Fetal Stomach	stomach
28	chr2:50975600-50975800	Enhancers	Psoas Muscle	Psoas
29	chr2:50975600-50976200	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
30	chr2:50975800-50976200	Active TSS	Brain Anterior Caudate	brain
31	chr2:50975800-50976200	Active TSS	Brain Hippocampus Middle	brain
32	chr2:50975800-50976200	Active TSS	Brain Substantia Nigra	brain
33	chr2:50975800-50976200	Enhancers	Fetal Kidney	kidney
34	chr2:50975800-50976600	Weak transcription	Fetal Stomach	stomach
35	chr2:50975800-50977000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr2:50975800-50978400	Weak transcription	Fetal Brain Male	brain
37	chr2:50976000-50977200	Enhancers	Brain Cingulate Gyrus	brain
38	chr2:50976000-50978000	Weak transcription	Psoas Muscle	Psoas
39	chr2:50976000-50978600	Weak transcription	Fetal Muscle Leg	muscle
40	chr2:50976200-50976600	Enhancers	Brain Inferior Temporal Lobe	brain
41	chr2:50976200-50976800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr2:50976200-50977400	Enhancers	Brain Hippocampus Middle	brain
43	chr2:50976200-50978200	Weak transcription	Brain Germinal Matrix	brain
44	chr2:50976200-50982800	Weak transcription	Brain Substantia Nigra	brain
45	chr2:50976400-50976600	Enhancers	Duodenum Smooth Muscle	Duodenum
46	chr2:50976600-50979800	Enhancers	Fetal Stomach	stomach
47	chr2:50976600-50983200	Weak transcription	Brain Inferior Temporal Lobe	brain
48	chr2:50976800-50977400	Weak transcription	Fetal Brain Female	brain
49	chr2:50976800-50978200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr2:50976800-50978200	Weak transcription	Duodenum Smooth Muscle	Duodenum

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