Variant report

Variant	esv2751896
Chromosome Location	chr2:50976171-51040820
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	chr2:51003545-51003679	IMR90	lung:	n/a	n/a
2	CEBPB	chr2:51039958-51040191	HepG2	liver:	n/a	n/a
3	CHD2	chr2:51020103-51020131	GM12878	blood:	n/a	n/a
4	CTCF	chr2:51013640-51013790	AG04450	lung:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
5	CTCF	chr2:51040238-51040274	A549	lung:	n/a	n/a
6	CTCF	chr2:51015540-51015690	HCT-116	colon:	n/a	n/a
7	CTCF	chr2:51013540-51013690	HCT-116	colon:	n/a	n/a
8	CTCF	chr2:50978545-50978604	Medullo	brain:	n/a	n/a
9	CTCF	chr2:51013620-51013770	HCT-116	colon:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
10	CTCF	chr2:51013580-51013730	WERI-Rb-1	eye:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
11	CTCF	chr2:50978500-50978650	HMEC	breast:	n/a	n/a
12	CTCF	chr2:50978582-50978614	Kidney_OC	kidney:	n/a	n/a
13	CTCF	chr2:51013578-51013819	Medullo	brain:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
14	CTCF	chr2:51013675-51013707	K562	blood:	n/a	chr2:51013679-51013695 chr2:51013678-51013696
15	CTCF	chr2:51013600-51013750	BE2_C	brain:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
16	CTCF	chr2:51009820-51009970	AG04450	lung:	n/a	chr2:51009841-51009854
17	CTCF	chr2:51009804-51009856	Hela-S3	cervix:	n/a	chr2:51009841-51009854
18	CTCF	chr2:51013600-51013750	NHEK	skin:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
19	CTCF	chr2:51013660-51013810	RPTEC	kidney:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
20	CTCF	chr2:51013640-51013790	RPTEC	kidney:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
21	CTCF	chr2:51009720-51009870	AG04450	lung:	n/a	chr2:51009841-51009854
22	CTCF	chr2:50978500-50978650	BE2_C	brain:	n/a	n/a
23	CTCF	chr2:51013607-51013764	Kidney_OC	kidney:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
24	CTCF	chr2:51013640-51013790	HRPEpiC	eye:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
25	CTCF	chr2:51013623-51013763	Hela-S3	cervix:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
26	CTCF	chr2:51013540-51013690	GM12866	blood:	n/a	n/a
27	CTCF	chr2:51013620-51013770	SK-N-SH_RA	brain:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
28	CTCF	chr2:51013610-51013718	HUVEC	blood vessel:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
29	CTCF	chr2:50976420-50976570	Caco-2	colon:	n/a	n/a
30	CTCF	chr2:51008900-51009050	Caco-2	colon:	n/a	n/a
31	CTCF	chr2:51013580-51013730	HRE	kidney:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
32	CTCF	chr2:51013560-51013710	HBMEC	blood vessel:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
33	CTCF	chr2:51013660-51013810	GM12873	blood:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
34	CTCF	chr2:51013620-51013770	WERI-Rb-1	eye:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
35	CTCF	chr2:51013580-51013730	AG04450	lung:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
36	CTCF	chr2:51009680-51009830	HRE	kidney:	n/a	n/a
37	CTCF	chr2:51009760-51009910	HBMEC	blood vessel:	n/a	chr2:51009841-51009854
38	CTCF	chr2:51009780-51009930	Caco-2	colon:	n/a	chr2:51009841-51009854
39	CTCF	chr2:51013580-51013730	HRPEpiC	eye:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
40	CTCF	chr2:51013600-51013750	HEK293	kidney:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
41	CTCF	chr2:51013600-51013750	HepG2	liver:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
42	CTCF	chr2:51040080-51040230	GM12874	blood:	n/a	n/a
43	ESR1	chr2:51036590-51036975	ECC-1	luminal epithelium:	n/a	n/a
44	ESR1	chr2:51036670-51036984	ECC-1	luminal epithelium:	n/a	n/a
45	ESR1	chr2:51031536-51031804	ECC-1	luminal epithelium:	n/a	chr2:51031705-51031722 chr2:51031705-51031720 chr2:51031704-51031721
46	ESR1	chr2:51036504-51036992	ECC-1	luminal epithelium:	n/a	n/a
47	ESR1	chr2:51036616-51037084	ECC-1	luminal epithelium:	n/a	n/a
48	FAM48A	chr2:50991708-50991886	GM12878	blood:	n/a	n/a
49	FOS	chr2:50978765-50979109	MCF10A-Er-Src	breast:	n/a	chr2:50978943-50978952 chr2:50978943-50978950
50	FOS	chr2:51009823-51010023	MCF10A-Er-Src	breast:	n/a	chr2:51009920-51009929 chr2:51009922-51009933 chr2:51009921-51009930 chr2:51009919-51009931

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:50992829-50992879	GM06990	blood:	n/a
2	chr2:50992829-50992879	HCF	heart:	n/a
3	chr2:51001003-51001053	NHDF-neo	bronchial:	n/a
4	chr2:51001003-51001053	H1-hESC	embryonic stem cell:	embryo
5	chr2:50992829-50992879	HL-60	blood:	n/a
6	chr2:50992829-50992879	AoSMC	blood vessel:	n/a
7	chr2:50992829-50992879	Hepatocyte	liver:	n/a
8	chr2:51001003-51001053	K562	blood:	n/a
9	chr2:51001003-51001053	SAEC	small airway:	n/a
10	chr2:50992829-50992879	GM12892	blood:	n/a
11	chr2:50992829-50992879	HAEpiC	amniotic membrane:	n/a
12	chr2:50992829-50992879	ProgFib	skin:	n/a
13	chr2:50992829-50992879	NHDF-neo	bronchial:	n/a
14	chr2:51001003-51001053	SK-N-SH_RA	brain:	n/a
15	chr2:51001003-51001053	PANC-1	pancreas:	n/a
16	chr2:50992829-50992879	ECC-1	luminal epithelium:	n/a
17	chr2:50992829-50992879	Hela-S3	cervix:	n/a
18	chr2:51001003-51001053	GM06990	blood:	n/a
19	chr2:51001003-51001053	AG10803	skin:	n/a
20	chr2:50992829-50992879	HCPEpiC	choroid plexus:	n/a
21	chr2:50992829-50992879	HRCEpiC	kidney:	n/a
22	chr2:51001003-51001053	AG09309	skin:	n/a
23	chr2:51001003-51001053	SKMC	muscle:	n/a
24	chr2:50992829-50992879	HIPEpiC	eye:	n/a
25	chr2:50992829-50992879	CMK	blood:	n/a
26	chr2:51001003-51001053	SK-N-MC	brain:	n/a
27	chr2:51001003-51001053	GM19239	blood:	n/a
28	chr2:51001003-51001053	GM12892	blood:	n/a
29	chr2:50992829-50992879	HNPCEpiC	eye:	n/a
30	chr2:50992829-50992879	K562	blood:	n/a
31	chr2:51001003-51001053	HRE	kidney:	n/a
32	chr2:50992829-50992879	MCF10A-Er-Src	breast:	n/a
33	chr2:50992829-50992879	HPAEpiC	pulmonary alveolar:	n/a
34	chr2:50992829-50992879	GM19239	blood:	n/a
35	chr2:51001003-51001053	HepG2	liver:	n/a
36	chr2:50992829-50992879	RPTEC	kidney:	n/a
37	chr2:51001003-51001053	HNPCEpiC	eye:	n/a
38	chr2:51001003-51001053	HEEpiC	esophagus:	n/a
39	chr2:50992829-50992879	HCT-116	colon:	n/a
40	chr2:50992829-50992879	HRE	kidney:	n/a
41	chr2:51001003-51001053	Jurkat	blood:	n/a
42	chr2:50992829-50992879	AG10803	skin:	n/a
43	chr2:51001003-51001053	MCF-7	breast:	n/a
44	chr2:50992829-50992879	HEK293	kidney:	embryo
45	chr2:51001003-51001053	ovcar-3	ovarian:	n/a
46	chr2:51001003-51001053	ProgFib	skin:	n/a
47	chr2:51001003-51001053	GM12891	blood:	n/a
48	chr2:51001003-51001053	PFSK-1	brain:	n/a
49	chr2:51001003-51001053	RPTEC	kidney:	n/a
50	chr2:51001003-51001053	T-47D	breast:	n/a

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

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

Extended variants
information (count: 2236 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:2236 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3842845	chr2:50976171-50976172	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs140530544	chr2:50976219-50976220	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs565852512	chr2:50976242-50976243	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs536520133	chr2:50976243-50976244	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs9679335	chr2:50976245-50976246	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs201923710	chr2:50976258-50976259	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs571714069	chr2:50976270-50976271	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs544342182	chr2:50976275-50976276	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs556238217	chr2:50976298-50976299	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs17041012	chr2:50976324-50976325	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs545085310	chr2:50976336-50976337	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs529325350	chr2:50976353-50976354	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs112544065	chr2:50976411-50976412	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs560507603	chr2:50976443-50976444	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs3842981	chr2:50976459-50976460	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs543287661	chr2:50976479-50976480	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs3901491	chr2:50976485-50976486	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs531937959	chr2:50976518-50976519	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs182836366	chr2:50976520-50976521	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs17041013	chr2:50976615-50976616	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs370149469	chr2:50976623-50976624	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs547098772	chr2:50976705-50976706	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs115266082	chr2:50976727-50976728	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs187919206	chr2:50976762-50976763	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs192310265	chr2:50976804-50976805	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs542578229	chr2:50976806-50976807	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs554840632	chr2:50976820-50976821	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs3850329	chr2:50976852-50976853	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs536852720	chr2:50976874-50976875	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs145624630	chr2:50976886-50976887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs138325042	chr2:50976972-50976973	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs551127675	chr2:50976980-50976981	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs184385116	chr2:50977002-50977003	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs553911054	chr2:50977025-50977026	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs572394058	chr2:50977054-50977055	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs570922165	chr2:50977110-50977111	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs533593168	chr2:50977168-50977169	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs531226242	chr2:50977187-50977188	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs189316081	chr2:50977189-50977190	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs561569279	chr2:50977216-50977217	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs532002335	chr2:50977223-50977224	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs544046196	chr2:50977233-50977234	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs542138616	chr2:50977240-50977241	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs546831013	chr2:50977275-50977276	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs192746255	chr2:50977297-50977298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs142892351	chr2:50977311-50977312	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs72837053	chr2:50977426-50977427	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs574415381	chr2:50977445-50977446	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs200379485	chr2:50977488-50977489	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs67759712	chr2:50977490-50977491	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

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
Schizophrenia	20967226	CNVD

Chromatin state (count:287 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:50972200-50978200	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr2:50974400-50976200	Enhancers	Brain Germinal Matrix	brain
3	chr2:50974400-50978200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr2:50975000-50976800	Enhancers	Fetal Brain Female	brain
5	chr2:50975200-50977200	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr2:50975600-50976200	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
7	chr2:50975800-50976200	Active TSS	Brain Anterior Caudate	brain
8	chr2:50975800-50976200	Active TSS	Brain Hippocampus Middle	brain
9	chr2:50975800-50976200	Active TSS	Brain Substantia Nigra	brain
10	chr2:50975800-50976200	Enhancers	Fetal Kidney	kidney
11	chr2:50975800-50976600	Weak transcription	Fetal Stomach	stomach
12	chr2:50975800-50977000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr2:50975800-50978400	Weak transcription	Fetal Brain Male	brain
14	chr2:50976000-50977200	Enhancers	Brain Cingulate Gyrus	brain
15	chr2:50976000-50978000	Weak transcription	Psoas Muscle	Psoas
16	chr2:50976000-50978600	Weak transcription	Fetal Muscle Leg	muscle
17	chr2:50976200-50976600	Enhancers	Brain Inferior Temporal Lobe	brain
18	chr2:50976200-50976800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr2:50976200-50977400	Enhancers	Brain Hippocampus Middle	brain
20	chr2:50976200-50978200	Weak transcription	Brain Germinal Matrix	brain
21	chr2:50976200-50982800	Weak transcription	Brain Substantia Nigra	brain
22	chr2:50976400-50976600	Enhancers	Duodenum Smooth Muscle	Duodenum
23	chr2:50976600-50979800	Enhancers	Fetal Stomach	stomach
24	chr2:50976600-50983200	Weak transcription	Brain Inferior Temporal Lobe	brain
25	chr2:50976800-50977400	Weak transcription	Fetal Brain Female	brain
26	chr2:50976800-50978200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr2:50976800-50978200	Weak transcription	Duodenum Smooth Muscle	Duodenum
28	chr2:50977000-50982200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr2:50977200-50978400	Weak transcription	Cortex derived primary cultured neurospheres	brain
30	chr2:50977400-50983600	Weak transcription	Brain Hippocampus Middle	brain
31	chr2:50977400-50984400	Enhancers	Fetal Brain Female	brain
32	chr2:50978200-50978800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr2:50978200-50979200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr2:50978200-50979200	Enhancers	Colon Smooth Muscle	Colon
35	chr2:50978200-50979400	Enhancers	Duodenum Smooth Muscle	Duodenum
36	chr2:50978200-50979600	Enhancers	Rectal Smooth Muscle	rectum
37	chr2:50978200-50980400	Enhancers	Brain Germinal Matrix	brain
38	chr2:50978200-50980400	Enhancers	Pancreatic Islets	Pancreatic Islet
39	chr2:50978400-50978800	Enhancers	NH-A	brain
40	chr2:50978400-50980800	Enhancers	Cortex derived primary cultured neurospheres	brain
41	chr2:50978400-50984400	Enhancers	Fetal Brain Male	brain
42	chr2:50978600-50978800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr2:50978600-50979200	Enhancers	Fetal Muscle Leg	muscle
44	chr2:50978800-50979400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr2:50979200-50982200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr2:50979200-50982200	Weak transcription	Fetal Muscle Leg	muscle
47	chr2:50979400-50979600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
48	chr2:50979400-50980800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr2:50979600-50982400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
50	chr2:50980200-50981000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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