Variant report

Variant	esv2757179
Chromosome Location	chr6:75525739-75625251
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:414)
CpG islands
(count:122)
Chromatin interactive
region (count:7)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:414 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:75566931-75567251	HepG2	liver:	n/a	n/a
2	BACH1	chr6:75557714-75557743	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr6:75566891-75567091	HepG2	liver:	n/a	n/a
4	CEBPB	chr6:75588856-75589356	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr6:75601837-75602086	IMR90	lung:	n/a	n/a
6	CEBPB	chr6:75588847-75589314	IMR90	lung:	n/a	n/a
7	CEBPB	chr6:75588829-75589194	A549	lung:	n/a	n/a
8	CEBPB	chr6:75566890-75567103	A549	lung:	n/a	n/a
9	CEBPB	chr6:75558084-75558360	HepG2	liver:	n/a	chr6:75558204-75558215
10	CEBPB	chr6:75611552-75611724	HepG2	liver:	n/a	chr6:75611594-75611605 chr6:75611594-75611607
11	CHD2	chr6:75588862-75589275	Hela-S3	cervix:	n/a	n/a
12	CTCF	chr6:75584180-75584330	AG04450	lung:	n/a	n/a
13	CTCF	chr6:75599451-75599519	HUVEC	blood vessel:	n/a	n/a
14	CTCF	chr6:75599380-75599530	AG10803	skin:	n/a	n/a
15	CTCF	chr6:75580360-75580510	HRPEpiC	eye:	n/a	n/a
16	CTCF	chr6:75580280-75580430	GM12878	blood:	n/a	n/a
17	CTCF	chr6:75599455-75599648	GM12878	blood:	n/a	n/a
18	CTCF	chr6:75609120-75609270	HRE	kidney:	n/a	n/a
19	CTCF	chr6:75609160-75609310	AG09319	gingival:	n/a	n/a
20	CTCF	chr6:75609220-75609370	GM12873	blood:	n/a	n/a
21	CTCF	chr6:75599440-75599590	HMF	breast:	n/a	n/a
22	CTCF	chr6:75599440-75599590	HCPEpiC	choroid plexus:	n/a	n/a
23	CTCF	chr6:75609160-75609310	GM12878	blood:	n/a	n/a
24	CTCF	chr6:75609173-75609377	HepG2	liver:	n/a	n/a
25	CTCF	chr6:75580380-75580530	HPF	lung:	n/a	n/a
26	CTCF	chr6:75609180-75609330	HBMEC	blood vessel:	n/a	n/a
27	CTCF	chr6:75613643-75613721	Kidney_OC	kidney:	n/a	n/a
28	CTCF	chr6:75588720-75588870	HEEpiC	esophagus:	n/a	n/a
29	CTCF	chr6:75609140-75609290	HCM	heart:	n/a	n/a
30	CTCF	chr6:75609235-75609281	K562	blood:	n/a	n/a
31	CTCF	chr6:75582389-75582544	Hela-S3	cervix:	n/a	n/a
32	CTCF	chr6:75580260-75580410	BJ	skin:	n/a	n/a
33	CTCF	chr6:75609135-75609454	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr6:75599420-75599570	HMEC	breast:	n/a	n/a
35	CTCF	chr6:75580340-75580490	GM12865	blood:	n/a	n/a
36	CTCF	chr6:75609182-75609375	MCF-7	breast:	n/a	n/a
37	CTCF	chr6:75609106-75609471	HepG2	liver:	n/a	n/a
38	CTCF	chr6:75609180-75609330	HPF	lung:	n/a	n/a
39	CTCF	chr6:75609215-75609400	GM12878	blood:	n/a	n/a
40	CTCF	chr6:75582475-75582527	GM10266	blood:	n/a	n/a
41	CTCF	chr6:75580500-75580650	GM12864	blood:	n/a	n/a
42	CTCF	chr6:75609160-75609310	HVMF	connective:	n/a	n/a
43	CTCF	chr6:75609180-75609330	AG10803	skin:	n/a	n/a
44	CTCF	chr6:75580260-75580410	HepG2	liver:	n/a	n/a
45	CTCF	chr6:75582380-75582530	GM12864	blood:	n/a	n/a
46	CTCF	chr6:75582424-75582487	GM19238	blood:	n/a	n/a
47	CTCF	chr6:75580460-75580610	RPTEC	kidney:	n/a	n/a
48	CTCF	chr6:75608980-75609130	HFF-Myc	foreskin:	n/a	n/a
49	CTCF	chr6:75609220-75609370	AG09309	skin:	n/a	n/a
50	CTCF	chr6:75609180-75609330	HAc	cerebellar:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:75589206-75589256	GM06990	blood:	n/a
2	chr6:75589206-75589256	HMEC	breast:	n/a
3	chr6:75589206-75589256	K562	blood:	n/a
4	chr6:75583742-75583792	ProgFib	skin:	n/a
5	chr6:75583742-75583792	PrEC	prostate:	n/a
6	chr6:75589206-75589256	HUVEC	blood vessel:	n/a
7	chr6:75589206-75589256	HAEpiC	amniotic membrane:	n/a
8	chr6:75583742-75583792	HNPCEpiC	eye:	n/a
9	chr6:75583742-75583792	MCF-7	breast:	n/a
10	chr6:75583742-75583792	PFSK-1	brain:	n/a
11	chr6:75589206-75589256	AG09309	skin:	n/a
12	chr6:75589206-75589256	HRPEpiC	eye:	n/a
13	chr6:75589206-75589256	NH-A	brain:	n/a
14	chr6:75589206-75589256	Hela-S3	cervix:	n/a
15	chr6:75583742-75583792	HAEpiC	amniotic membrane:	n/a
16	chr6:75583742-75583792	HIPEpiC	eye:	n/a
17	chr6:75583742-75583792	RPTEC	kidney:	n/a
18	chr6:75589206-75589256	NT2-D1	testis:	n/a
19	chr6:75583742-75583792	CMK	blood:	n/a
20	chr6:75589206-75589256	BE2_C	brain:	n/a
21	chr6:75583742-75583792	HEK293	kidney:	embryo
22	chr6:75583742-75583792	Hepatocyte	liver:	n/a
23	chr6:75583742-75583792	GM12892	blood:	n/a
24	chr6:75583742-75583792	GM12878	blood:	n/a
25	chr6:75583742-75583792	K562	blood:	n/a
26	chr6:75589206-75589256	ovcar-3	ovarian:	n/a
27	chr6:75589206-75589256	Caco-2	colon:	n/a
28	chr6:75589206-75589256	HepG2	liver:	n/a
29	chr6:75589206-75589256	IMR90	lung:	fetal
30	chr6:75583742-75583792	GM19239	blood:	n/a
31	chr6:75583742-75583792	BE2_C	brain:	n/a
32	chr6:75589206-75589256	AG10803	skin:	n/a
33	chr6:75589206-75589256	T-47D	breast:	n/a
34	chr6:75583742-75583792	AG10803	skin:	n/a
35	chr6:75583742-75583792	IMR90	lung:	fetal
36	chr6:75583742-75583792	SK-N-SH_RA	brain:	n/a
37	chr6:75583742-75583792	HEEpiC	esophagus:	n/a
38	chr6:75583742-75583792	HRE	kidney:	n/a
39	chr6:75589206-75589256	AG04449	skin:	fetal
40	chr6:75589206-75589256	HCM	heart:	n/a
41	chr6:75589206-75589256	BJ	skin:	n/a
42	chr6:75583742-75583792	HRCEpiC	kidney:	n/a
43	chr6:75589206-75589256	U87	brain:	n/a
44	chr6:75583742-75583792	HL-60	blood:	n/a
45	chr6:75589206-75589256	HCPEpiC	choroid plexus:	n/a
46	chr6:75589206-75589256	Jurkat	blood:	n/a
47	chr6:75589206-75589256	HEEpiC	esophagus:	n/a
48	chr6:75589206-75589256	HRE	kidney:	n/a
49	chr6:75589206-75589256	AG09319	gingival:	n/a
50	chr6:75589206-75589256	GM12892	blood:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:75610525..75612245-chr6:75914237..75915878,2	MCF-7	breast:
2	chr6:75609148..75609683-chr6:75913367..75914426,3	MCF-7	breast:
3	chr6:75608999..75611267-chr6:75912636..75915418,2	MCF-7	breast:
4	chr6:75622208..75624628-chr6:75629968..75631581,2	MCF-7	breast:
5	chr6:75589124..75590939-chr6:75914285..75915811,2	MCF-7	breast:
6	chr6:75609173..75609713-chr6:75911685..75912571,2	MCF-7	breast:
7	chr6:75623758..75626363-chr6:75914057..75916388,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COL12A1-2	chr6:75558793-75560200	NONHSAT113595

No data

Variant related genes	Relation type
ENSG00000219736	TF binding region
ENSG00000219736	CpG island
ENSG00000111799	chromatin interactions

Extended variants
information (count: 1747 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:1747 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536451161	chr6:75535822-75535823	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs554439264	chr6:75535849-75535850	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs368328767	chr6:75535880-75535881	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs569898885	chr6:75535911-75535912	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs573125863	chr6:75535948-75535949	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs140472286	chr6:75535962-75535963	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs150477935	chr6:75535988-75535989	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs577603846	chr6:75535990-75535991	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs182632481	chr6:75536011-75536012	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs557948521	chr6:75536015-75536016	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs57421982	chr6:75536039-75536040	Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs576130443	chr6:75536080-75536081	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs530878478	chr6:75536112-75536113	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs185904944	chr6:75536149-75536150	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs561311792	chr6:75536152-75536153	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs528811984	chr6:75536176-75536177	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs546977767	chr6:75536181-75536182	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs571305826	chr6:75536188-75536189	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs142652165	chr6:75536200-75536201	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs189974065	chr6:75536221-75536222	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs550549700	chr6:75536223-75536224	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs568995804	chr6:75536224-75536225	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs535950052	chr6:75536234-75536235	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs554777258	chr6:75536249-75536250	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs79570447	chr6:75536397-75536398	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs115068488	chr6:75536414-75536415	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs558435754	chr6:75536428-75536429	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs117147262	chr6:75536429-75536430	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs115377065	chr6:75536434-75536435	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs182587940	chr6:75536439-75536440	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs9352162	chr6:75536443-75536444	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs200285178	chr6:75536453-75536454	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs542736562	chr6:75536455-75536456	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs187246739	chr6:75536471-75536472	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs528671716	chr6:75536472-75536473	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs111872955	chr6:75536496-75536497	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs565582707	chr6:75536497-75536498	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs56306321	chr6:75536547-75536548	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs532827223	chr6:75536556-75536557	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs550611743	chr6:75536574-75536575	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs376433214	chr6:75536578-75536579	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs545952289	chr6:75536594-75536595	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs386702757	chr6:75538835-75538836	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs7753921	chr6:75538836-75538837	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs575987506	chr6:75538857-75538858	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs536601277	chr6:75538931-75538932	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs113148354	chr6:75538940-75538941	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs16820	chr6:75539046-75539047	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs541236665	chr6:75539065-75539066	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs16885704	chr6:75539142-75539143	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:98)

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
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	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
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Systemic lupus erythematosus	17503323	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Lung cancer	18438408	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
Prostate cancer	16573809	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ovarian cancer	17437010	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Mental retardation	17124404	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Multiple myeloma	16616336	CNVD
Acute myeloid leukemia	16864856	CNVD
Follicular lymphoma	17699855	CNVD
Breast cancer	17133270	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Developmental delay	21147756	CNVD
Chronic lymphocytic leukemia	21546498	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
low-grade B-cell lymphoma tumor	18367492	CNVD
Lung adenocarcinoma	21935476	CNVD
Myelodysplastic syndrome	18508791	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	23813976	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:181 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:75535800-75536200	Enhancers	Skeletal Muscle Female	skeletal muscle
2	chr6:75535800-75536600	Enhancers	Primary hematopoietic stem cells short term culture	blood
3	chr6:75536000-75536400	Active TSS	Ovary	ovary
4	chr6:75536000-75536400	Enhancers	NHDF-Ad	bronchial
5	chr6:75538800-75539200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr6:75544400-75545200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr6:75561000-75561400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr6:75561000-75561400	Enhancers	Adipose Nuclei	Adipose
9	chr6:75561000-75561800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr6:75561000-75561800	Enhancers	NHDF-Ad	bronchial
11	chr6:75561000-75562200	Enhancers	HSMM	muscle
12	chr6:75561000-75562200	Enhancers	HSMMtube	muscle
13	chr6:75561000-75562400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr6:75561200-75561800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr6:75562200-75563400	Weak transcription	HSMM	muscle
16	chr6:75562400-75562800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr6:75562800-75563800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr6:75563000-75563600	Enhancers	Rectal Smooth Muscle	rectum
19	chr6:75563000-75564000	Enhancers	Duodenum Smooth Muscle	Duodenum
20	chr6:75563200-75563600	Enhancers	Ovary	ovary
21	chr6:75563200-75563800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr6:75563600-75563800	Enhancers	HSMM	muscle
23	chr6:75563600-75564400	Weak transcription	Ovary	ovary
24	chr6:75564400-75564600	Enhancers	Ovary	ovary
25	chr6:75571000-75577000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr6:75572400-75575400	Enhancers	Ovary	ovary
27	chr6:75573000-75573400	Enhancers	Fetal Kidney	kidney
28	chr6:75575200-75575400	Enhancers	HSMMtube	muscle
29	chr6:75575400-75576200	Weak transcription	Ovary	ovary
30	chr6:75575400-75580400	Weak transcription	HSMMtube	muscle
31	chr6:75576200-75576600	Enhancers	Ovary	ovary
32	chr6:75576400-75577200	Enhancers	HSMM	muscle
33	chr6:75576400-75577800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr6:75577000-75577600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr6:75577200-75580600	Weak transcription	HSMM	muscle
36	chr6:75577600-75580000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr6:75577800-75580000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr6:75580000-75580800	Enhancers	HepG2	liver
39	chr6:75580000-75584400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr6:75580000-75584400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr6:75580400-75582000	Enhancers	HSMMtube	muscle
42	chr6:75580600-75582200	Enhancers	HSMM	muscle
43	chr6:75581000-75582200	Enhancers	HMEC	breast
44	chr6:75581000-75584400	Enhancers	Osteobl	bone
45	chr6:75581200-75582000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr6:75581400-75582000	Enhancers	NHEK	skin
47	chr6:75581600-75582000	Enhancers	Muscle Satellite Cultured Cells	--
48	chr6:75581600-75582000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr6:75581800-75584200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr6:75582000-75582600	ZNF genes & repeats	HSMMtube	muscle

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links