Variant report

Variant	nsv999179
Chromosome Location	chr2:72561463-72761103
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:883)
CpG islands
(count:61)
Chromatin interactive
region (count:38)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:883 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:72744986-72745715	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:72760857-72762181	K562	blood:	n/a	n/a
3	ARID3A	chr2:72665577-72665773	HepG2	liver:	n/a	n/a
4	ATF1	chr2:72753444-72753585	K562	blood:	n/a	n/a
5	ATF1	chr2:72741133-72741286	K562	blood:	n/a	n/a
6	ATF1	chr2:72760996-72761223	K562	blood:	n/a	n/a
7	ATF3	chr2:72594792-72595306	A549	lung:	n/a	n/a
8	BACH1	chr2:72741410-72741524	K562	blood:	n/a	n/a
9	BACH1	chr2:72675350-72675409	K562	blood:	n/a	n/a
10	BACH1	chr2:72719205-72719270	K562	blood:	n/a	n/a
11	BATF	chr2:72619978-72620200	GM12878	blood:	n/a	chr2:72620159-72620169
12	BCL3	chr2:72594632-72595392	A549	lung:	n/a	n/a
13	BCL3	chr2:72594727-72595339	A549	lung:	n/a	n/a
14	BHLHE40	chr2:72681407-72681607	K562	blood:	n/a	n/a
15	BHLHE40	chr2:72756167-72756234	A549	lung:	n/a	n/a
16	CBX3	chr2:72594934-72595318	HCT-116	colon:	n/a	n/a
17	CBX3	chr2:72613411-72613830	K562	blood:	n/a	n/a
18	CBX3	chr2:72613471-72613765	K562	blood:	n/a	n/a
19	CBX3	chr2:72760828-72761353	HCT-116	colon:	n/a	n/a
20	CCNT2	chr2:72760937-72761322	K562	blood:	n/a	n/a
21	CCNT2	chr2:72580873-72581066	K562	blood:	n/a	n/a
22	CCNT2	chr2:72578182-72578331	K562	blood:	n/a	n/a
23	CEBPB	chr2:72594490-72595360	A549	lung:	n/a	n/a
24	CEBPB	chr2:72745059-72745420	HepG2	liver:	n/a	n/a
25	CEBPB	chr2:72564350-72564473	H1-hESC	embryonic stem cell:	n/a	chr2:72564438-72564451 chr2:72564440-72564451 chr2:72564440-72564451 chr2:72564438-72564451
26	CEBPB	chr2:72594850-72595338	ECC-1	luminal epithelium:	n/a	n/a
27	CEBPB	chr2:72594678-72595345	A549	lung:	n/a	n/a
28	CEBPB	chr2:72724873-72725236	HepG2	liver:	n/a	chr2:72725049-72725060
29	CEBPB	chr2:72594624-72595341	A549	lung:	n/a	n/a
30	CEBPB	chr2:72608809-72609073	HepG2	liver:	n/a	chr2:72608920-72608933 chr2:72608920-72608931 chr2:72608922-72608933
31	CEBPB	chr2:72724869-72725242	IMR90	lung:	n/a	chr2:72725049-72725060
32	CEBPB	chr2:72651002-72651425	HepG2	liver:	n/a	chr2:72651151-72651162
33	CEBPB	chr2:72594709-72595362	HCT-116	colon:	n/a	n/a
34	CEBPB	chr2:72656744-72656880	A549	lung:	n/a	n/a
35	CEBPB	chr2:72665501-72665866	HepG2	liver:	n/a	n/a
36	CEBPB	chr2:72595079-72595208	K562	blood:	n/a	n/a
37	CEBPB	chr2:72724986-72725164	K562	blood:	n/a	chr2:72725049-72725060
38	CEBPB	chr2:72754595-72754903	HepG2	liver:	n/a	chr2:72754742-72754753
39	CEBPB	chr2:72594831-72595372	MCF-7	breast:	n/a	n/a
40	CEBPB	chr2:72758583-72758936	HCT-116	colon:	n/a	n/a
41	CEBPB	chr2:72754594-72754912	A549	lung:	n/a	chr2:72754742-72754753
42	CEBPB	chr2:72594952-72595290	HepG2	liver:	n/a	n/a
43	CEBPB	chr2:72584061-72584254	HepG2	liver:	n/a	chr2:72584153-72584164
44	CEBPB	chr2:72724883-72725175	A549	lung:	n/a	chr2:72725049-72725060
45	CEBPB	chr2:72594841-72595298	ECC-1	luminal epithelium:	n/a	n/a
46	CEBPB	chr2:72754565-72754972	K562	blood:	n/a	chr2:72754742-72754753
47	CEBPB	chr2:72758789-72758942	A549	lung:	n/a	n/a
48	CEBPB	chr2:72697631-72697718	HepG2	liver:	n/a	chr2:72697632-72697643
49	CEBPB	chr2:72651037-72651329	A549	lung:	n/a	chr2:72651151-72651162
50	CEBPB	chr2:72685384-72685612	Hela-S3	cervix:	n/a	chr2:72685499-72685512

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:72606914-72606964	AoSMC	blood vessel:	n/a
2	chr2:72606914-72606964	AG04450	lung:	fetal
3	chr2:72606914-72606964	HUVEC	blood vessel:	n/a
4	chr2:72606914-72606964	NT2-D1	testis:	n/a
5	chr2:72606914-72606964	T-47D	breast:	n/a
6	chr2:72606914-72606964	NH-A	brain:	n/a
7	chr2:72606914-72606964	SAEC	small airway:	n/a
8	chr2:72606914-72606964	LNCaP	prostate:	n/a
9	chr2:72606914-72606964	PFSK-1	brain:	n/a
10	chr2:72606914-72606964	MCF-7	breast:	n/a
11	chr2:72606914-72606964	ECC-1	luminal epithelium:	n/a
12	chr2:72606914-72606964	A549	lung:	n/a
13	chr2:72606914-72606964	Caco-2	colon:	n/a
14	chr2:72606914-72606964	ovcar-3	ovarian:	n/a
15	chr2:72606914-72606964	BE2_C	brain:	n/a
16	chr2:72606914-72606964	GM12878	blood:	n/a
17	chr2:72606914-72606964	NHDF-neo	bronchial:	n/a
18	chr2:72606914-72606964	GM06990	blood:	n/a
19	chr2:72606914-72606964	Hepatocyte	liver:	n/a
20	chr2:72606914-72606964	IMR90	lung:	fetal
21	chr2:72606914-72606964	HPAEpiC	pulmonary alveolar:	n/a
22	chr2:72606914-72606964	HEEpiC	esophagus:	n/a
23	chr2:72606914-72606964	SK-N-SH	brain:	n/a
24	chr2:72606914-72606964	HNPCEpiC	eye:	n/a
25	chr2:72606914-72606964	PANC-1	pancreas:	n/a
26	chr2:72606914-72606964	HCPEpiC	choroid plexus:	n/a
27	chr2:72606914-72606964	U87	brain:	n/a
28	chr2:72606914-72606964	HRE	kidney:	n/a
29	chr2:72606914-72606964	GM12891	blood:	n/a
30	chr2:72606914-72606964	HRPEpiC	eye:	n/a
31	chr2:72606914-72606964	Hela-S3	cervix:	n/a
32	chr2:72606914-72606964	SKMC	muscle:	n/a
33	chr2:72606914-72606964	AG10803	skin:	n/a
34	chr2:72606914-72606964	AG09319	gingival:	n/a
35	chr2:72606914-72606964	MCF10A-Er-Src	breast:	n/a
36	chr2:72606914-72606964	NHBE	bronchial:	n/a
37	chr2:72606914-72606964	RPTEC	kidney:	n/a
38	chr2:72606914-72606964	HCT-116	colon:	n/a
39	chr2:72606914-72606964	NB4	blood:	n/a
40	chr2:72606914-72606964	HCM	heart:	n/a
41	chr2:72606914-72606964	AG09309	skin:	n/a
42	chr2:72606914-72606964	SK-N-SH_RA	brain:	n/a
43	chr2:72606914-72606964	SK-N-MC	brain:	n/a
44	chr2:72606914-72606964	ProgFib	skin:	n/a
45	chr2:72606914-72606964	AG04449	skin:	fetal
46	chr2:72606914-72606964	HRCEpiC	kidney:	n/a
47	chr2:72606914-72606964	HEK293	kidney:	embryo
48	chr2:72606914-72606964	GM12892	blood:	n/a
49	chr2:72606914-72606964	K562	blood:	n/a
50	chr2:72606914-72606964	PrEC	prostate:	n/a

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:72744464..72746896-chr2:72747784..72749596,2	K562	blood:
2	chr2:72651011..72654002-chr2:72655484..72657938,2	MCF-7	breast:
3	chr2:72573103..72574031-chr2:188995710..188996539,2	MCF-7	breast:
4	chr2:72738252..72740072-chr2:72743033..72744721,2	K562	blood:
5	chr2:72701558..72703531-chr2:72704901..72708933,3	MCF-7	breast:
6	chr2:72691074..72693045-chr2:72701878..72703474,2	MCF-7	breast:
7	chr2:72684137..72687084-chr2:72706108..72708534,2	MCF-7	breast:
8	chr2:72747909..72750021-chr2:72752476..72754330,3	K562	blood:
9	chr2:72734670..72737032-chr2:72745367..72747114,2	MCF-7	breast:
10	chr2:72737047..72739752-chr2:72743033..72745282,2	K562	blood:
11	chr2:72744464..72746896-chr2:72747784..72749596,2	K562	blood:
12	chr2:72616102..72617981-chr2:72733250..72735254,2	K562	blood:
13	chr2:72563559..72566519-chr2:72566611..72568121,2	K562	blood:
14	chr2:72615828..72618063-chr2:72620028..72621701,2	MCF-7	breast:
15	chr2:72643084..72645013-chr2:72652645..72655633,3	MCF-7	breast:
16	chr2:72613280..72613780-chr8:19325545..19326087,2	MCF-7	breast:
17	chr2:72616102..72617981-chr2:72733250..72735254,2	K562	blood:
18	chr2:72643084..72645013-chr2:72652645..72655633,3	MCF-7	breast:
19	chr2:72576055..72577738-chr2:72579767..72581620,2	K562	blood:
20	chr2:72651011..72654002-chr2:72655484..72657938,2	MCF-7	breast:
21	chr2:72747909..72750021-chr2:72752476..72754330,3	K562	blood:
22	chr2:72734670..72737032-chr2:72745367..72747114,2	MCF-7	breast:
23	chr2:72675277..72678684-chr2:72678721..72682329,4	MCF-7	breast:
24	chr2:72701558..72703531-chr2:72704901..72708933,3	MCF-7	breast:
25	chr2:72607420..72609302-chr2:72612337..72614241,2	MCF-7	breast:
26	chr2:72676869..72679264-chr2:72682562..72684885,2	MCF-7	breast:
27	chr2:72684137..72687084-chr2:72706108..72708534,2	MCF-7	breast:
28	chr2:72563559..72566519-chr2:72566611..72568121,2	K562	blood:
29	chr2:72691074..72693045-chr2:72701878..72703474,2	MCF-7	breast:
30	chr2:72676869..72679264-chr2:72682562..72684885,2	MCF-7	breast:
31	chr2:72738252..72740072-chr2:72743033..72744721,2	K562	blood:
32	chr2:72607420..72609302-chr2:72612337..72614241,2	MCF-7	breast:
33	chr2:72675277..72678684-chr2:72678721..72682329,4	MCF-7	breast:
34	chr2:72377572..72378539-chr2:72594368..72595601,4	MCF-7	breast:
35	chr2:72615828..72618063-chr2:72620028..72621701,2	MCF-7	breast:
36	chr2:72721174..72724904-chr2:72725415..72727814,3	K562	blood:
37	chr2:72721978..72724058-chr2:72749672..72751274,2	MCF-7	breast:
38	chr2:72737047..72739752-chr2:72743033..72745282,2	K562	blood:

No data

Variant related genes	Relation type
EXOC6B	TF binding region
EXOC6B	CpG island
ENSG00000144036	chromatin interactions

Extended variants
information (count: 6703 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:6703 , 50 per page) page: 1 2 3 4 5 6 7 ... 135

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568775682	chr2:72561489-72561490	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs539371872	chr2:72561528-72561529	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs187439929	chr2:72561579-72561580	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs373838022	chr2:72561593-72561594	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs557777061	chr2:72561610-72561611	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs143730687	chr2:72561646-72561647	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs573167059	chr2:72561776-72561777	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs534027739	chr2:72561855-72561856	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs571933030	chr2:72561859-72561860	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs555581559	chr2:72561865-72561866	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs540791429	chr2:72561897-72561898	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs62149281	chr2:72561946-72561947	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs574221890	chr2:72561968-72561969	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs146140262	chr2:72561980-72561981	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs562975214	chr2:72562015-72562016	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs577958359	chr2:72562056-72562057	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs111624023	chr2:72562101-72562102	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs375284555	chr2:72562106-72562107	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs191567398	chr2:72562121-72562122	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs566348239	chr2:72562161-72562162	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs183996739	chr2:72562177-72562178	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs371853759	chr2:72562200-72562201	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs376972688	chr2:72562211-72562212	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs542787587	chr2:72562229-72562230	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs531899657	chr2:72562252-72562253	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs138173346	chr2:72562299-72562300	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs568894991	chr2:72562350-72562351	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs539102533	chr2:72562385-72562386	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs187994725	chr2:72562399-72562400	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs566801802	chr2:72562410-72562411	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs376535642	chr2:72562426-72562427	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs534065706	chr2:72562457-72562458	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs560683374	chr2:72562501-72562502	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs555669309	chr2:72562575-72562576	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs573906885	chr2:72562583-72562584	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs375630276	chr2:72562678-72562679	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs371021664	chr2:72562679-72562680	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs537995178	chr2:72562681-72562682	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs70963124	chr2:72562721-72562722	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs181039711	chr2:72562724-72562725	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs373196531	chr2:72562769-72562770	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs185596755	chr2:72562814-72562815	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs370969434	chr2:72562899-72562900	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs34077784	chr2:72562918-72562919	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs578041134	chr2:72562993-72562994	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs545117055	chr2:72563028-72563029	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs560090948	chr2:72563068-72563069	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs377378299	chr2:72563150-72563151	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs542929555	chr2:72563322-72563323	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs149558042	chr2:72563481-72563482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:53)

Disease	PMID	Source
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
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Lung cancer	18438408	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Developmental delay	21147756	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Hepatocellular carcinoma	16750200	CNVD
Renal cell carcinoma	18765545	CNVD
Myxofibrosarcoma	16751306	CNVD
Myelofibrosis	22110671	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Acute myeloid leukemia	21251322	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:1264 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:72531200-72594800	Weak transcription	Esophagus	oesophagus
2	chr2:72537200-72567800	Weak transcription	Ovary	ovary
3	chr2:72538600-72567800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr2:72551800-72563400	Weak transcription	Primary T cells from cord blood	blood
5	chr2:72552600-72568600	Weak transcription	Fetal Brain Male	brain
6	chr2:72553000-72563600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr2:72553600-72562200	Weak transcription	Left Ventricle	heart
8	chr2:72553600-72576000	Weak transcription	Fetal Heart	heart
9	chr2:72553800-72594600	Weak transcription	Aorta	Aorta
10	chr2:72554000-72562000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr2:72554400-72567600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr2:72558000-72568800	Weak transcription	HMEC	breast
13	chr2:72559200-72607400	Weak transcription	Liver	Liver
14	chr2:72560000-72561600	Weak transcription	Brain Germinal Matrix	brain
15	chr2:72560400-72562000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr2:72560600-72563000	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr2:72560600-72563200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr2:72560600-72594800	Weak transcription	Pancreas	Pancrea
19	chr2:72560800-72561600	Strong transcription	Adipose Nuclei	Adipose
20	chr2:72560800-72562400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr2:72561400-72561600	Enhancers	Brain Cingulate Gyrus	brain
22	chr2:72561400-72562200	Enhancers	HSMMtube	muscle
23	chr2:72561400-72562800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr2:72561400-72562800	Enhancers	Brain Hippocampus Middle	brain
25	chr2:72561600-72562200	Weak transcription	Brain Cingulate Gyrus	brain
26	chr2:72561600-72562200	Enhancers	Brain Germinal Matrix	brain
27	chr2:72561600-72562200	Active TSS	Brain Substantia Nigra	brain
28	chr2:72561600-72563000	Enhancers	Brain Inferior Temporal Lobe	brain
29	chr2:72561600-72571800	Weak transcription	Adipose Nuclei	Adipose
30	chr2:72561800-72562000	Enhancers	Brain Anterior Caudate	brain
31	chr2:72562000-72562200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr2:72562000-72562400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr2:72562000-72562400	Flanking Active TSS	Brain Anterior Caudate	brain
34	chr2:72562000-72562400	Enhancers	Fetal Muscle Leg	muscle
35	chr2:72562200-72562400	Enhancers	Brain Cingulate Gyrus	brain
36	chr2:72562200-72562400	Enhancers	Brain Substantia Nigra	brain
37	chr2:72562200-72562400	Enhancers	Left Ventricle	heart
38	chr2:72562200-72562600	Flanking Active TSS	HSMMtube	muscle
39	chr2:72562200-72563000	Enhancers	Fetal Lung	lung
40	chr2:72562200-72563200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr2:72562400-72562600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr2:72562400-72566600	Weak transcription	Left Ventricle	heart
43	chr2:72562600-72562800	Enhancers	HSMMtube	muscle
44	chr2:72563000-72563400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr2:72563200-72564400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr2:72564600-72564800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr2:72566600-72566800	Enhancers	Left Ventricle	heart
48	chr2:72566600-72568000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr2:72567600-72567800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr2:72567600-72568200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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