Variant report

Variant	esv1840176
Chromosome Location	chr6:134268822-134274297
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	ARID3A	chr6:134272926-134274538	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:134273021-134273329	K562	blood:	n/a	n/a
3	ARID3A	chr6:134273753-134274425	K562	blood:	n/a	n/a
4	ATF1	chr6:134274098-134274417	K562	blood:	n/a	n/a
5	ATF2	chr6:134273540-134274487	GM12878	blood:	n/a	n/a
6	ATF2	chr6:134273664-134274427	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr6:134273943-134274375	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr6:134273616-134274446	GM12878	blood:	n/a	n/a
9	ATF3	chr6:134274124-134274368	K562	blood:	n/a	chr6:134274199-134274208
10	BACH1	chr6:134273134-134273398	K562	blood:	n/a	n/a
11	BACH1	chr6:134273056-134273937	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr6:134274101-134274422	GM12878	blood:	n/a	n/a
13	BCL11A	chr6:134274097-134274388	GM12878	blood:	n/a	chr6:134274106-134274115 chr6:134274200-134274209
14	BCL3	chr6:134273984-134274542	A549	lung:	n/a	chr6:134274106-134274115 chr6:134274200-134274209 chr6:134274522-134274535
15	BCL3	chr6:134273992-134274541	A549	lung:	n/a	chr6:134274106-134274115 chr6:134274200-134274209 chr6:134274522-134274535
16	BCLAF1	chr6:134273990-134274645	K562	blood:	n/a	chr6:134274106-134274115 chr6:134274200-134274209 chr6:134274522-134274535
17	BCLAF1	chr6:134273913-134274618	GM12878	blood:	n/a	chr6:134274106-134274115 chr6:134274200-134274209 chr6:134274522-134274535
18	BCLAF1	chr6:134272983-134274536	GM12878	blood:	n/a	chr6:134273461-134273470 chr6:134274106-134274115 chr6:134274200-134274209 chr6:134274522-134274535
19	BCLAF1	chr6:134273080-134273855	GM12878	blood:	n/a	chr6:134273461-134273470
20	BCLAF1	chr6:134273925-134274610	K562	blood:	n/a	chr6:134274106-134274115 chr6:134274200-134274209 chr6:134274522-134274535
21	BHLHE40	chr6:134273947-134274585	K562	blood:	n/a	n/a
22	BHLHE40	chr6:134272994-134274455	GM12878	blood:	n/a	n/a
23	BRCA1	chr6:134273632-134274424	H1-hESC	embryonic stem cell:	n/a	n/a
24	BRCA1	chr6:134274045-134274476	HepG2	liver:	n/a	n/a
25	BRCA1	chr6:134273655-134274429	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr6:134273323-134273598	HepG2	liver:	n/a	n/a
27	CBX3	chr6:134273866-134274622	HCT-116	colon:	n/a	n/a
28	CBX3	chr6:134273952-134274606	K562	blood:	n/a	n/a
29	CCNT2	chr6:134273859-134274864	K562	blood:	n/a	chr6:134274811-134274820 chr6:134274199-134274208
30	CCNT2	chr6:134273140-134273546	K562	blood:	n/a	chr6:134273429-134273438
31	CEBPB	chr6:134274266-134274281	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr6:134274182-134274376	HepG2	liver:	n/a	n/a
33	CEBPB	chr6:134273452-134274528	GM12878	blood:	n/a	n/a
34	CEBPB	chr6:134273557-134274496	ECC-1	luminal epithelium:	n/a	n/a
35	CEBPD	chr6:134273997-134274609	HepG2	liver:	n/a	n/a
36	CHD1	chr6:134273456-134274507	GM12878	blood:	n/a	chr6:134273783-134273792
37	CHD2	chr6:134273188-134274497	HepG2	liver:	n/a	chr6:134273783-134273792
38	CHD2	chr6:134273167-134273217	K562	blood:	n/a	n/a
39	CHD2	chr6:134273535-134274571	K562	blood:	n/a	chr6:134273783-134273792
40	CHD2	chr6:134273576-134274585	H1-hESC	embryonic stem cell:	n/a	chr6:134273783-134273792
41	CHD2	chr6:134273108-134274868	Hela-S3	cervix:	n/a	chr6:134273783-134273792
42	CHD2	chr6:134273044-134274595	GM12878	blood:	n/a	chr6:134273783-134273792
43	CREB1	chr6:134274048-134274647	H1-hESC	embryonic stem cell:	n/a	n/a
44	CREB1	chr6:134273869-134274667	K562	blood:	n/a	n/a
45	CREB1	chr6:134273920-134274695	GM12878	blood:	n/a	n/a
46	CREB1	chr6:134273938-134274837	HepG2	liver:	n/a	n/a
47	CREB1	chr6:134273940-134274639	H1-hESC	embryonic stem cell:	n/a	n/a
48	CREB1	chr6:134273956-134274586	K562	blood:	n/a	n/a
49	CREB1	chr6:134273998-134274566	A549	lung:	n/a	n/a
50	CTBP2	chr6:134273033-134274598	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:134274110-134274160	H1-hESC	embryonic stem cell:	embryo
2	chr6:134274107-134274157	AG04449	skin:	fetal
3	chr6:134274110-134274160	H1-hESC	embryonic stem cell:	embryo
4	chr6:134274107-134274157	AG04449	skin:	fetal
5	chr6:134272463-134272513	U87	brain:	n/a
6	chr6:134270138-134270188	NB4	blood:	n/a
7	chr6:134270138-134270188	HL-60	blood:	n/a
8	chr6:134274110-134274160	AG04450	lung:	fetal
9	chr6:134273465-134273515	ECC-1	luminal epithelium:	n/a
10	chr6:134270138-134270188	SK-N-MC	brain:	n/a
11	chr6:134274107-134274157	HRE	kidney:	n/a
12	chr6:134270138-134270188	HRPEpiC	eye:	n/a
13	chr6:134274110-134274160	CMK	blood:	n/a
14	chr6:134270138-134270188	AG04450	lung:	fetal
15	chr6:134272463-134272513	GM19239	blood:	n/a
16	chr6:134274110-134274160	HCF	heart:	n/a
17	chr6:134274107-134274157	K562	blood:	n/a
18	chr6:134274008-134274058	HAEpiC	amniotic membrane:	n/a
19	chr6:134272463-134272513	HRPEpiC	eye:	n/a
20	chr6:134274110-134274160	U87	brain:	n/a
21	chr6:134274107-134274157	BE2_C	brain:	n/a
22	chr6:134274107-134274157	PFSK-1	brain:	n/a
23	chr6:134273564-134273614	BE2_C	brain:	n/a
24	chr6:134270138-134270188	RPTEC	kidney:	n/a
25	chr6:134273199-134273249	NH-A	brain:	n/a
26	chr6:134274110-134274160	HNPCEpiC	eye:	n/a
27	chr6:134273564-134273614	ECC-1	luminal epithelium:	n/a
28	chr6:134273121-134273171	AG04450	lung:	fetal
29	chr6:134272463-134272513	CMK	blood:	n/a
30	chr6:134274110-134274160	Hepatocyte	liver:	n/a
31	chr6:134274110-134274160	SAEC	small airway:	n/a
32	chr6:134273564-134273614	PANC-1	pancreas:	n/a
33	chr6:134273564-134273614	HL-60	blood:	n/a
34	chr6:134273564-134273614	HCPEpiC	choroid plexus:	n/a
35	chr6:134274286-134274336	K562	blood:	n/a
36	chr6:134273121-134273171	SK-N-MC	brain:	n/a
37	chr6:134273199-134273249	HRE	kidney:	n/a
38	chr6:134273564-134273614	PrEC	prostate:	n/a
39	chr6:134274110-134274160	NB4	blood:	n/a
40	chr6:134274107-134274157	U87	brain:	n/a
41	chr6:134273465-134273515	MCF10A-Er-Src	breast:	n/a
42	chr6:134274008-134274058	HL-60	blood:	n/a
43	chr6:134273465-134273515	ProgFib	skin:	n/a
44	chr6:134273199-134273249	HEK293	kidney:	embryo
45	chr6:134274286-134274336	HIPEpiC	eye:	n/a
46	chr6:134274107-134274157	HCM	heart:	n/a
47	chr6:134273465-134273515	HCPEpiC	choroid plexus:	n/a
48	chr6:134270138-134270188	NHDF-neo	bronchial:	n/a
49	chr6:134273199-134273249	GM06990	blood:	n/a
50	chr6:134273121-134273171	PANC-1	pancreas:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:133132887..133135811-chr6:134273188..134277510,5	K562	blood:
2	chr6:134259055..134262632-chr6:134266342..134269518,3	K562	blood:
3	chr6:134260984..134262645-chr6:134269778..134271680,2	K562	blood:
4	chr6:134273314..134277341-chr6:134371733..134374606,4	K562	blood:

Variant related genes	Relation type
TBPL1	TF binding region
TBPL1	CpG island
ENSG00000112306	chromatin interactions
ENSG00000146411	chromatin interactions

Extended variants
information (count: 168 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:168 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs228867	chr6:134268822-134268823	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs183685515	chr6:134268833-134268834	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs542950645	chr6:134268963-134268964	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs375800812	chr6:134268981-134268982	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs369942172	chr6:134268983-134268984	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs541820301	chr6:134269058-134269059	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs561942571	chr6:134269079-134269080	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs77909489	chr6:134269184-134269185	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs541183390	chr6:134269198-134269199	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs560269520	chr6:134269313-134269314	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs187002360	chr6:134269338-134269339	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs552440355	chr6:134269346-134269347	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs562764983	chr6:134269391-134269392	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs6938805	chr6:134269392-134269393	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs78487977	chr6:134269466-134269467	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs150995831	chr6:134269569-134269570	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs80292618	chr6:134269605-134269606	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs191835577	chr6:134269622-134269623	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs373585943	chr6:134269724-134269725	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs142749236	chr6:134269798-134269799	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs370051933	chr6:134269799-134269800	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs570246037	chr6:134269825-134269826	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs539637311	chr6:134269885-134269886	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs556386085	chr6:134269936-134269937	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs140816779	chr6:134269939-134269940	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs149753959	chr6:134269955-134269956	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs146760338	chr6:134269957-134269958	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs572372555	chr6:134269960-134269961	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs541445989	chr6:134270036-134270037	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs543077160	chr6:134270072-134270073	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs564411164	chr6:134270074-134270075	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs564618890	chr6:134270131-134270132	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs578176193	chr6:134270215-134270216	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs182163776	chr6:134270276-134270277	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs562679644	chr6:134270458-134270459	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs186900361	chr6:134270556-134270557	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs193236829	chr6:134270580-134270581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs78114420	chr6:134270607-134270608	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs546986380	chr6:134270619-134270620	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs527276249	chr6:134270640-134270641	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs559339753	chr6:134270686-134270687	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs547410371	chr6:134270738-134270739	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs185746976	chr6:134270763-134270764	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs539150658	chr6:134270794-134270795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs549923151	chr6:134270802-134270803	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs569932743	chr6:134270811-134270812	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs4896016	chr6:134270849-134270850	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs527937958	chr6:134270871-134270872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs34082514	chr6:134270880-134270881	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs55705079	chr6:134271016-134271017	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Autism	22495311	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Gastric cancer	17908304	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Lung adenocarcinoma	21935476	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21785460	CNVD
Kartagener syndrome	16639409	CNVD
Breast cancer	17133270	CNVD
Follicular lymphoma	18703704	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	18641027	CNVD

Chromatin state (count:336 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:134266600-134272400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr6:134266800-134272200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr6:134267000-134272200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr6:134267800-134271600	Enhancers	Liver	Liver
5	chr6:134268000-134269000	Enhancers	K562	blood
6	chr6:134268000-134270200	Enhancers	Rectal Mucosa Donor 31	rectum
7	chr6:134268000-134270400	Enhancers	Duodenum Mucosa	Duodenum
8	chr6:134268000-134270400	Enhancers	Pancreas	Pancrea
9	chr6:134268200-134269200	Weak transcription	Rectal Mucosa Donor 29	rectum
10	chr6:134268200-134269600	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr6:134268200-134270000	Weak transcription	Gastric	stomach
12	chr6:134268200-134270600	Enhancers	Stomach Mucosa	stomach
13	chr6:134268400-134272200	Weak transcription	Aorta	Aorta
14	chr6:134268600-134272400	Weak transcription	Fetal Brain Female	brain
15	chr6:134269000-134272400	Weak transcription	K562	blood
16	chr6:134269200-134270000	Enhancers	Rectal Mucosa Donor 29	rectum
17	chr6:134269600-134270200	Enhancers	Sigmoid Colon	Sigmoid Colon
18	chr6:134270000-134270400	Enhancers	Gastric	stomach
19	chr6:134270000-134272400	Weak transcription	Rectal Mucosa Donor 29	rectum
20	chr6:134270200-134272400	Weak transcription	Rectal Mucosa Donor 31	rectum
21	chr6:134270200-134272400	Weak transcription	Sigmoid Colon	Sigmoid Colon
22	chr6:134270400-134272200	Weak transcription	Duodenum Mucosa	Duodenum
23	chr6:134270400-134272200	Weak transcription	Gastric	stomach
24	chr6:134270400-134272400	Weak transcription	Pancreas	Pancrea
25	chr6:134270600-134272200	Weak transcription	Stomach Mucosa	stomach
26	chr6:134271600-134272000	Weak transcription	Liver	Liver
27	chr6:134272000-134272600	Enhancers	Liver	Liver
28	chr6:134272200-134272400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr6:134272200-134272400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr6:134272200-134272400	Enhancers	Breast Myoepithelial Primary Cells	Breast
31	chr6:134272200-134272400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr6:134272200-134272400	Enhancers	Muscle Satellite Cultured Cells	--
33	chr6:134272200-134272400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr6:134272200-134272400	Enhancers	Adipose Nuclei	Adipose
35	chr6:134272200-134272400	Flanking Active TSS	Aorta	Aorta
36	chr6:134272200-134272400	Enhancers	Brain Anterior Caudate	brain
37	chr6:134272200-134272400	Enhancers	Brain Cingulate Gyrus	brain
38	chr6:134272200-134272400	Enhancers	Brain Inferior Temporal Lobe	brain
39	chr6:134272200-134272400	Enhancers	Brain Substantia Nigra	brain
40	chr6:134272200-134272400	Enhancers	Duodenum Mucosa	Duodenum
41	chr6:134272200-134272400	Enhancers	Fetal Lung	lung
42	chr6:134272200-134272400	Enhancers	A549	lung
43	chr6:134272200-134272400	Enhancers	GM12878-XiMat	blood
44	chr6:134272200-134272400	Enhancers	HSMM	muscle
45	chr6:134272200-134272400	Enhancers	HSMMtube	muscle
46	chr6:134272200-134272400	Enhancers	NHDF-Ad	bronchial
47	chr6:134272200-134272400	Enhancers	NHEK	skin
48	chr6:134272200-134272600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr6:134272200-134272600	Enhancers	Primary B cells from peripheral blood	blood
50	chr6:134272200-134272600	Enhancers	Primary T cells fromperipheralblood	blood

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