Variant report

Variant	esv1837685
Chromosome Location	chr6:71997278-71998880
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:353)
CpG islands
(count:306)
Chromatin interactive
region (count:1)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:353 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr6:71998373-71998481	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr6:71997741-71997991	GM12878	blood:	n/a	n/a
3	BCL11A	chr6:71997761-71998058	GM12878	blood:	n/a	n/a
4	BHLHE40	chr6:71997710-71998207	GM12878	blood:	n/a	n/a
5	BHLHE40	chr6:71998494-71998737	GM12878	blood:	n/a	n/a
6	BRCA1	chr6:71997992-71998249	Hela-S3	cervix:	n/a	n/a
7	CCNT2	chr6:71998354-71998725	K562	blood:	n/a	n/a
8	CEBPB	chr6:71997872-71998666	Hela-S3	cervix:	n/a	n/a
9	CHD1	chr6:71998606-71999437	H1-hESC	embryonic stem cell:	n/a	n/a
10	CHD1	chr6:71998399-71998744	GM12878	blood:	n/a	n/a
11	CHD2	chr6:71997795-71998257	GM12878	blood:	n/a	n/a
12	CHD2	chr6:71997852-71998706	Hela-S3	cervix:	n/a	n/a
13	CREB1	chr6:71997993-71998698	A549	lung:	n/a	n/a
14	CTBP2	chr6:71997949-71998546	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr6:71998420-71998570	HCFaa	heart:	n/a	n/a
16	CTCF	chr6:71998420-71998570	HCPEpiC	choroid plexus:	n/a	n/a
17	CTCF	chr6:71998319-71998676	IMR90	lung:	n/a	chr6:71998393-71998406 chr6:71998368-71998377
18	CTCF	chr6:71997940-71998090	WERI-Rb-1	eye:	n/a	n/a
19	CTCF	chr6:71998420-71998570	AoAF	blood vessel:	n/a	n/a
20	CTCF	chr6:71998409-71998650	GM10266	blood:	n/a	n/a
21	CTCF	chr6:71998425-71998630	MCF-7	breast:	n/a	n/a
22	CTCF	chr6:71998480-71998630	GM12868	blood:	n/a	n/a
23	CTCF	chr6:71998469-71998596	GM10248	blood:	n/a	n/a
24	CTCF	chr6:71998456-71998632	LNCaP	prostate:	n/a	n/a
25	CTCF	chr6:71998407-71998663	MCF-7	breast:	n/a	n/a
26	CTCF	chr6:71998420-71998570	AG04450	lung:	n/a	n/a
27	CTCF	chr6:71998400-71998550	AG10803	skin:	n/a	n/a
28	CTCF	chr6:71998440-71998590	Caco-2	colon:	n/a	n/a
29	CTCF	chr6:71998420-71998570	WI-38	lung:	n/a	n/a
30	CTCF	chr6:71998281-71998749	GM12878	blood:	n/a	chr6:71998393-71998406 chr6:71998368-71998377
31	CTCF	chr6:71998380-71998530	WERI-Rb-1	eye:	n/a	chr6:71998393-71998406
32	CTCF	chr6:71998397-71998636	SK-N-SH_RA	brain:	n/a	n/a
33	CTCF	chr6:71998391-71998681	GM19238	blood:	n/a	chr6:71998393-71998406
34	CTCF	chr6:71998740-71998890	AG04449	skin:	n/a	n/a
35	CTCF	chr6:71998420-71998570	GM12878	blood:	n/a	n/a
36	CTCF	chr6:71998455-71998626	Lung_OC	lung:	n/a	n/a
37	CTCF	chr6:71998437-71998589	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr6:71997960-71998110	HRPEpiC	eye:	n/a	n/a
39	CTCF	chr6:71998452-71998580	MCF-7	breast:	n/a	n/a
40	CTCF	chr6:71998440-71998590	RPTEC	kidney:	n/a	n/a
41	CTCF	chr6:71998386-71998680	MCF-7	breast:	n/a	chr6:71998393-71998406
42	CTCF	chr6:71998400-71998614	ProgFib	skin:	n/a	n/a
43	CTCF	chr6:71998420-71998603	A549	lung:	n/a	n/a
44	CTCF	chr6:71997758-71999716	SK-N-SH	brain:	n/a	chr6:71998393-71998406 chr6:71998368-71998377 chr6:71999230-71999238 chr6:71998968-71998981
45	CTCF	chr6:71998440-71998590	GM12869	blood:	n/a	n/a
46	CTCF	chr6:71998444-71998587	GM13977	blood:	n/a	n/a
47	CTCF	chr6:71998440-71998590	GM12866	blood:	n/a	n/a
48	CTCF	chr6:71998460-71998610	GM12872	blood:	n/a	n/a
49	CTCF	chr6:71998460-71998610	GM12869	blood:	n/a	n/a
50	CTCF	chr6:71998412-71998615	Gliobla	brain:	n/a	n/a

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:71998385-71998435	HEK293	kidney:	embryo
2	chr6:71998385-71998435	HEK293	kidney:	embryo
3	chr6:71998385-71998435	RPTEC	kidney:	n/a
4	chr6:71998398-71998448	GM12891	blood:	n/a
5	chr6:71997462-71997512	HRCEpiC	kidney:	n/a
6	chr6:71998145-71998195	Hela-S3	cervix:	n/a
7	chr6:71998145-71998195	AoSMC	blood vessel:	n/a
8	chr6:71998145-71998195	AG04449	skin:	fetal
9	chr6:71998597-71998647	AG09309	skin:	n/a
10	chr6:71998398-71998448	AG04449	skin:	fetal
11	chr6:71997462-71997512	SK-N-MC	brain:	n/a
12	chr6:71998597-71998647	HCM	heart:	n/a
13	chr6:71998597-71998647	HIPEpiC	eye:	n/a
14	chr6:71998145-71998195	HRE	kidney:	n/a
15	chr6:71997462-71997512	ECC-1	luminal epithelium:	n/a
16	chr6:71998145-71998195	HCT-116	colon:	n/a
17	chr6:71997462-71997512	HCM	heart:	n/a
18	chr6:71998597-71998647	Hela-S3	cervix:	n/a
19	chr6:71997462-71997512	K562	blood:	n/a
20	chr6:71997462-71997512	PFSK-1	brain:	n/a
21	chr6:71998145-71998195	HEK293	kidney:	embryo
22	chr6:71997462-71997512	BJ	skin:	n/a
23	chr6:71998597-71998647	H1-hESC	embryonic stem cell:	embryo
24	chr6:71998385-71998435	GM12878	blood:	n/a
25	chr6:71998398-71998448	HAEpiC	amniotic membrane:	n/a
26	chr6:71998385-71998435	T-47D	breast:	n/a
27	chr6:71998385-71998435	HIPEpiC	eye:	n/a
28	chr6:71998597-71998647	PANC-1	pancreas:	n/a
29	chr6:71998385-71998435	K562	blood:	n/a
30	chr6:71997462-71997512	LNCaP	prostate:	n/a
31	chr6:71998398-71998448	HCT-116	colon:	n/a
32	chr6:71998398-71998448	HMEC	breast:	n/a
33	chr6:71998398-71998448	T-47D	breast:	n/a
34	chr6:71998398-71998448	BJ	skin:	n/a
35	chr6:71997462-71997512	Hepatocyte	liver:	n/a
36	chr6:71997462-71997512	GM12892	blood:	n/a
37	chr6:71997462-71997512	BE2_C	brain:	n/a
38	chr6:71998597-71998647	SK-N-MC	brain:	n/a
39	chr6:71998145-71998195	SK-N-SH	brain:	n/a
40	chr6:71998597-71998647	CMK	blood:	n/a
41	chr6:71997462-71997512	HCPEpiC	choroid plexus:	n/a
42	chr6:71998145-71998195	RPTEC	kidney:	n/a
43	chr6:71998398-71998448	ProgFib	skin:	n/a
44	chr6:71998398-71998448	HEK293	kidney:	embryo
45	chr6:71998145-71998195	H1-hESC	embryonic stem cell:	embryo
46	chr6:71998145-71998195	NB4	blood:	n/a
47	chr6:71998145-71998195	HCM	heart:	n/a
48	chr6:71997462-71997512	HRE	kidney:	n/a
49	chr6:71998398-71998448	MCF-7	breast:	n/a
50	chr6:71998385-71998435	ovcar-3	ovarian:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:71997812..71999868-chr6:72020711..72023495,2	MCF-7	breast:

No data

Variant related genes	Relation type
OGFRL1	TF binding region
ENSG00000232295	TF binding region
OGFRL1	CpG island
ENSG00000232295	CpG island
ENSG00000232295	chromatin interactions

Extended variants
information (count: 52 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:52 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2208845	chr6:71997278-71997279	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs548211833	chr6:71997316-71997317	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
3	rs566725537	chr6:71997340-71997341	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs2224656	chr6:71997447-71997448	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs552631571	chr6:71997472-71997473	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
6	rs570855670	chr6:71997495-71997496	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
7	rs144260990	chr6:71997517-71997518	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs574500091	chr6:71997530-71997531	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs531969483	chr6:71997532-71997533	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs201078388	chr6:71997633-71997634	Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs201682554	chr6:71997634-71997635	Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs143484938	chr6:71997635-71997636	Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs143360421	chr6:71997636-71997637	Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs113407919	chr6:71997637-71997638	Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
15	rs143680872	chr6:71997638-71997639	Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
16	rs67347683	chr6:71997645-71997646	Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
17	rs375346364	chr6:71997647-71997648	Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
18	rs560967044	chr6:71997686-71997687	Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
19	rs186667716	chr6:71997726-71997727	Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
20	rs536018024	chr6:71997729-71997730	Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
21	rs554181600	chr6:71997755-71997756	Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
22	rs190824811	chr6:71997795-71997796	Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
23	rs553603278	chr6:71997799-71997800	Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
24	rs143789687	chr6:71997822-71997823	Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs546088227	chr6:71997890-71997891	Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs564581183	chr6:71997983-71997984	Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs182643965	chr6:71997997-71997998	Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs185543093	chr6:71998023-71998024	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs6913383	chr6:71998031-71998032	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs529863981	chr6:71998070-71998071	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs548400030	chr6:71998108-71998109	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs560366265	chr6:71998114-71998115	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs190251500	chr6:71998131-71998132	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs527631947	chr6:71998139-71998140	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs6935796	chr6:71998162-71998163	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs570867124	chr6:71998166-71998167	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs116039266	chr6:71998198-71998199	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs182162213	chr6:71998222-71998223	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs568504710	chr6:71998224-71998225	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs535560449	chr6:71998258-71998259	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs554395015	chr6:71998283-71998284	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs546110366	chr6:71998412-71998413	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs562615714	chr6:71998422-71998423	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs557984940	chr6:71998550-71998551	Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs576453463	chr6:71998624-71998625	Active TSS Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs544160797	chr6:71998651-71998652	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs376036358	chr6:71998654-71998655	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs368114977	chr6:71998724-71998725	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs555871898	chr6:71998769-71998770	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs112585190	chr6:71998778-71998779	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
Chronic lymphocytic leukemia	21546498	CNVD
Gastrointestinal stromal cancer	20818650	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
Developmental delay	21147756	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
Breast cancer	21364760	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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	20409316	CNVD

Chromatin state (count:331 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:71988200-71997400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr6:71988200-71997400	Weak transcription	Left Ventricle	heart
3	chr6:71988400-71997800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr6:71991600-71997800	Weak transcription	Lung	lung
5	chr6:71992000-71997800	Weak transcription	Esophagus	oesophagus
6	chr6:71994200-71997800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr6:71994800-71997600	Weak transcription	Pancreas	Pancrea
8	chr6:71994800-71997800	Weak transcription	Gastric	stomach
9	chr6:71995200-71997400	Weak transcription	NHEK	skin
10	chr6:71995400-71997400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr6:71995600-71997600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr6:71995800-71997600	Enhancers	Psoas Muscle	Psoas
13	chr6:71996000-71997400	Enhancers	Primary monocytes fromperipheralblood	blood
14	chr6:71996200-71997600	Weak transcription	Spleen	Spleen
15	chr6:71996600-71997600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
16	chr6:71996600-71997600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr6:71996800-71997400	Enhancers	Primary B cells from peripheral blood	blood
18	chr6:71996800-71997400	Enhancers	Primary hematopoietic stem cells short term culture	blood
19	chr6:71996800-71997400	Enhancers	Adipose Nuclei	Adipose
20	chr6:71996800-71997600	Enhancers	Primary T cells fromperipheralblood	blood
21	chr6:71996800-71997600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
22	chr6:71996800-71997800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr6:71996800-71997800	Enhancers	Fetal Thymus	thymus
24	chr6:71996800-71997800	Enhancers	Stomach Mucosa	stomach
25	chr6:71996800-71998000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
26	chr6:71996800-71998200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
27	chr6:71997000-71997400	Enhancers	Primary T helper naive cells from peripheral blood	blood
28	chr6:71997000-71997400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr6:71997000-71997400	Enhancers	Brain Anterior Caudate	brain
30	chr6:71997000-71997400	Enhancers	Colon Smooth Muscle	Colon
31	chr6:71997000-71997400	Enhancers	Rectal Smooth Muscle	rectum
32	chr6:71997000-71997600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr6:71997000-71997600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr6:71997000-71997600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr6:71997000-71997600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
36	chr6:71997000-71997600	Enhancers	Primary T helper cells PMA-I stimulated	--
37	chr6:71997000-71997600	Enhancers	Primary T helper cells fromperipheralblood	blood
38	chr6:71997000-71997600	Enhancers	Liver	Liver
39	chr6:71997000-71997600	Enhancers	Duodenum Mucosa	Duodenum
40	chr6:71997000-71997600	Enhancers	Rectal Mucosa Donor 31	rectum
41	chr6:71997000-71997600	Enhancers	Skeletal Muscle Female	skeletal muscle
42	chr6:71997000-71997600	Enhancers	GM12878-XiMat	blood
43	chr6:71997000-71997600	Enhancers	Hela-S3	cervix
44	chr6:71997000-71997600	Enhancers	Osteobl	bone
45	chr6:71997000-71997800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
46	chr6:71997000-71997800	Enhancers	Primary T killer memory cells from peripheral blood	blood
47	chr6:71997000-71997800	Enhancers	Muscle Satellite Cultured Cells	--
48	chr6:71997000-71997800	Enhancers	Skeletal Muscle Male	skeletal muscle
49	chr6:71997000-71997800	Enhancers	HMEC	breast
50	chr6:71997000-71998000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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