Variant report

Variant	esv3447442
Chromosome Location	chr7:10985761-11013298
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:593)
CpG islands
(count:244)
Chromatin interactive
region (count:31)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:593 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:11013100-11013602	K562	blood:	n/a	n/a
2	ARID3A	chr7:11012565-11013705	HepG2	liver:	n/a	n/a
3	ATF1	chr7:10991707-10991852	K562	blood:	n/a	n/a
4	ATF1	chr7:11012682-11013593	K562	blood:	n/a	n/a
5	ATF2	chr7:11012410-11013687	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr7:11012550-11013322	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr7:11012605-11013331	GM12878	blood:	n/a	n/a
8	ATF2	chr7:11012559-11013715	GM12878	blood:	n/a	n/a
9	ATF3	chr7:11013239-11013674	A549	lung:	n/a	n/a
10	BACH1	chr7:11010694-11010942	K562	blood:	n/a	n/a
11	BCL3	chr7:11012933-11013671	A549	lung:	n/a	chr7:11013495-11013504
12	BCL3	chr7:11012756-11013758	A549	lung:	n/a	chr7:11013495-11013504
13	BHLHE40	chr7:11013181-11013689	GM12878	blood:	n/a	n/a
14	BHLHE40	chr7:11013168-11013601	K562	blood:	n/a	n/a
15	BRCA1	chr7:11012952-11013139	GM12878	blood:	n/a	n/a
16	BRCA1	chr7:11012774-11013200	H1-hESC	embryonic stem cell:	n/a	n/a
17	BRCA1	chr7:11012713-11013636	Hela-S3	cervix:	n/a	n/a
18	CBX3	chr7:11012418-11013716	K562	blood:	n/a	n/a
19	CBX3	chr7:11005849-11006118	K562	blood:	n/a	n/a
20	CBX3	chr7:10990636-10990997	K562	blood:	n/a	n/a
21	CBX3	chr7:11012620-11013355	K562	blood:	n/a	n/a
22	CCNT2	chr7:11013188-11013762	K562	blood:	n/a	n/a
23	CEBPB	chr7:11012683-11013136	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr7:11012677-11014062	HepG2	liver:	n/a	n/a
25	CEBPB	chr7:11012677-11013580	HepG2	liver:	n/a	n/a
26	CEBPB	chr7:11012593-11013441	A549	lung:	n/a	n/a
27	CEBPB	chr7:11012578-11013142	A549	lung:	n/a	n/a
28	CEBPB	chr7:11013113-11013634	K562	blood:	n/a	n/a
29	CEBPB	chr7:11012674-11013568	K562	blood:	n/a	n/a
30	CEBPB	chr7:11011010-11011069	K562	blood:	n/a	n/a
31	CEBPB	chr7:11012593-11013061	K562	blood:	n/a	n/a
32	CEBPB	chr7:11013171-11013378	HepG2	liver:	n/a	n/a
33	CEBPB	chr7:11012554-11013607	Hela-S3	cervix:	n/a	n/a
34	CEBPD	chr7:11013129-11013710	HepG2	liver:	n/a	n/a
35	CEBPD	chr7:11013232-11013766	HepG2	liver:	n/a	n/a
36	CEBPD	chr7:11012755-11013120	HepG2	liver:	n/a	n/a
37	CEBPZ	chr7:10987055-10987078	HepG2	liver:	n/a	n/a
38	CHD1	chr7:11012948-11013744	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD2	chr7:11012510-11013526	K562	blood:	n/a	n/a
40	CHD2	chr7:11012537-11014303	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD2	chr7:11012710-11013620	HepG2	liver:	n/a	n/a
42	CHD2	chr7:11012492-11014344	Hela-S3	cervix:	n/a	n/a
43	CREB1	chr7:11013183-11013735	A549	lung:	n/a	n/a
44	CREB1	chr7:11012742-11013016	A549	lung:	n/a	n/a
45	CREB1	chr7:11012694-11013019	ECC-1	luminal epithelium:	n/a	n/a
46	CTCF	chr7:11006998-11007053	Gliobla	brain:	n/a	n/a
47	CTCF	chr7:11006940-11007090	GM12872	blood:	n/a	n/a
48	CTCF	chr7:11006920-11007070	Caco-2	colon:	n/a	n/a
49	CTCF	chr7:11006943-11007083	MCF-7	breast:	n/a	n/a
50	CTCF	chr7:10996320-10996470	HepG2	liver:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:11010872-11010922	NH-A	brain:	n/a
2	chr7:11012873-11012923	HRE	kidney:	n/a
3	chr7:11012873-11012923	MCF10A-Er-Src	breast:	n/a
4	chr7:11010872-11010922	MCF10A-Er-Src	breast:	n/a
5	chr7:11010872-11010922	GM19239	blood:	n/a
6	chr7:11013274-11013324	BJ	skin:	n/a
7	chr7:11010872-11010922	HCPEpiC	choroid plexus:	n/a
8	chr7:11010872-11010922	GM12878	blood:	n/a
9	chr7:11012967-11013017	ovcar-3	ovarian:	n/a
10	chr7:11010872-11010922	Jurkat	blood:	n/a
11	chr7:11010872-11010922	HCF	heart:	n/a
12	chr7:11010872-11010922	T-47D	breast:	n/a
13	chr7:11010872-11010922	BE2_C	brain:	n/a
14	chr7:11012873-11012923	HIPEpiC	eye:	n/a
15	chr7:11013274-11013324	PrEC	prostate:	n/a
16	chr7:11012873-11012923	PrEC	prostate:	n/a
17	chr7:11013274-11013324	SAEC	small airway:	n/a
18	chr7:11010872-11010922	HUVEC	blood vessel:	n/a
19	chr7:11012967-11013017	U87	brain:	n/a
20	chr7:11010872-11010922	HepG2	liver:	n/a
21	chr7:11012967-11013017	HEK293	kidney:	embryo
22	chr7:11013274-11013324	SK-N-MC	brain:	n/a
23	chr7:11013274-11013324	HIPEpiC	eye:	n/a
24	chr7:11012873-11012923	HMEC	breast:	n/a
25	chr7:11012967-11013017	NT2-D1	testis:	n/a
26	chr7:11012873-11012923	HCM	heart:	n/a
27	chr7:11013274-11013324	CMK	blood:	n/a
28	chr7:11012967-11013017	MCF10A-Er-Src	breast:	n/a
29	chr7:11012967-11013017	HMEC	breast:	n/a
30	chr7:11013274-11013324	BE2_C	brain:	n/a
31	chr7:11012967-11013017	IMR90	lung:	fetal
32	chr7:11013274-11013324	PANC-1	pancreas:	n/a
33	chr7:11012873-11012923	GM12891	blood:	n/a
34	chr7:11012873-11012923	SK-N-SH	brain:	n/a
35	chr7:11010872-11010922	HAEpiC	amniotic membrane:	n/a
36	chr7:11012873-11012923	SAEC	small airway:	n/a
37	chr7:11012967-11013017	HIPEpiC	eye:	n/a
38	chr7:11013274-11013324	HUVEC	blood vessel:	n/a
39	chr7:11013274-11013324	MCF10A-Er-Src	breast:	n/a
40	chr7:11010872-11010922	NHDF-neo	bronchial:	n/a
41	chr7:11010872-11010922	Hela-S3	cervix:	n/a
42	chr7:11012967-11013017	PFSK-1	brain:	n/a
43	chr7:11012967-11013017	NHDF-neo	bronchial:	n/a
44	chr7:11012967-11013017	HRE	kidney:	n/a
45	chr7:11012873-11012923	A549	lung:	n/a
46	chr7:11012967-11013017	SK-N-MC	brain:	n/a
47	chr7:11010872-11010922	HRPEpiC	eye:	n/a
48	chr7:11012873-11012923	RPTEC	kidney:	n/a
49	chr7:11013274-11013324	RPTEC	kidney:	n/a
50	chr7:11013274-11013324	Caco-2	colon:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:11012451..11014446-chr7:11075009..11077346,2	MCF-7	breast:
2	chr7:10975906..10982429-chr7:11007978..11018673,26	K562	blood:
3	chr7:11005901..11008185-chr7:11010044..11012149,2	K562	blood:
4	chr7:10972277..10974447-chr7:11011761..11013440,2	K562	blood:
5	chr7:10996449..11000162-chr7:11009366..11013332,3	K562	blood:
6	chr7:10994945..10997006-chr7:11013339..11016151,2	MCF-7	breast:
7	chr7:10994214..10996545-chr7:11013291..11015040,3	MCF-7	breast:
8	chr7:10993579..10996514-chr7:10997193..10998993,2	K562	blood:
9	chr7:11010971..11012619-chr7:11259384..11261240,2	MCF-7	breast:
10	chr7:10993579..10996514-chr7:10997193..10998993,2	K562	blood:
11	chr7:10985009..10987966-chr7:11011919..11013774,2	MCF-7	breast:
12	chr11:73019220..73019808-chr7:11012749..11013563,2	HCT-116	colon:
13	chr7:10988102..10989982-chr7:10992834..10996627,3	MCF-7	breast:
14	chr7:11006402..11010250-chr7:11012259..11015737,5	K562	blood:
15	chr7:11012908..11015544-chr7:11049769..11053521,4	MCF-7	breast:
16	chr7:10978325..10981149-chr7:10995847..10998453,3	K562	blood:
17	chr7:10978326..10980800-chr7:10996010..10997979,3	MCF-7	breast:
18	chr7:11012745..11013588-chrX:16737490..16738055,2	Hela-S3	cervix:
19	chr7:11004791..11009411-chr7:11011969..11015268,6	MCF-7	breast:
20	chr7:11013088..11016193-chr7:11045661..11047742,3	MCF-7	breast:
21	chr7:11005901..11008185-chr7:11010044..11012149,2	K562	blood:
22	chr7:10978101..10982429-chr7:11011509..11017731,20	K562	blood:
23	chr7:10977305..10982144-chr7:11011875..11016071,10	MCF-7	breast:
24	chr7:10970436..10972192-chr7:11007402..11009320,2	K562	blood:
25	chr7:10988102..10989982-chr7:10992834..10996627,3	MCF-7	breast:
26	chr7:10979309..10981149-chr7:10995607..10997523,2	K562	blood:
27	chr7:10978242..10981238-chr7:11011671..11015550,7	MCF-7	breast:
28	chr7:11007370..11009612-chr7:11011024..11013340,2	MCF-7	breast:
29	chr7:10993482..10995624-chr7:11021410..11023892,2	K562	blood:
30	chr7:10996449..11000162-chr7:11009366..11013332,3	K562	blood:
31	chr7:11007370..11009612-chr7:11011024..11013340,2	MCF-7	breast:

No data

Variant related genes	Relation type
PHF14	TF binding region
PHF14	CpG island
ENSG00000110237	chromatin interactions
ENSG00000169895	chromatin interactions
ENSG00000230370	chromatin interactions
ENSG00000189043	chromatin interactions
ENSG00000271185	chromatin interactions
ENSG00000106443	chromatin interactions

Extended variants
information (count: 984 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:984 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs112623663	chr7:10985762-10985763	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs218972	chr7:10985774-10985775	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs533778352	chr7:10985797-10985798	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs578000055	chr7:10985850-10985851	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs371673456	chr7:10985860-10985861	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs537399229	chr7:10985866-10985867	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs139613177	chr7:10985875-10985876	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs574358233	chr7:10985902-10985903	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs543261422	chr7:10985929-10985930	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs375390161	chr7:10985948-10985949	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs527321027	chr7:10986032-10986033	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs369508630	chr7:10986063-10986064	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs185054838	chr7:10986076-10986077	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs564017653	chr7:10986101-10986102	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs149723333	chr7:10986133-10986134	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs553575860	chr7:10986140-10986141	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs563266843	chr7:10986190-10986191	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs73678337	chr7:10986191-10986192	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs2353336	chr7:10986194-10986195	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs539235040	chr7:10986254-10986255	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs189019054	chr7:10986258-10986259	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs145550449	chr7:10986273-10986274	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs551859041	chr7:10986329-10986330	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs556357903	chr7:10986330-10986331	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs369507039	chr7:10986334-10986335	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs575847905	chr7:10986346-10986347	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs75315634	chr7:10986371-10986372	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs557359597	chr7:10986405-10986406	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs547089030	chr7:10986455-10986456	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs567650133	chr7:10986475-10986476	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs180984023	chr7:10986498-10986499	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs148429416	chr7:10986541-10986542	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs573426017	chr7:10986590-10986591	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs6970176	chr7:10986634-10986635	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs59634596	chr7:10986700-10986701	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs548974149	chr7:10986735-10986736	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs147585834	chr7:10986738-10986739	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs186317784	chr7:10986760-10986761	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs6970358	chr7:10986773-10986774	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs369819666	chr7:10986799-10986800	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs559342867	chr7:10986802-10986803	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs142005604	chr7:10986809-10986810	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs145747053	chr7:10986826-10986827	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs373439031	chr7:10986834-10986835	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs218971	chr7:10986882-10986883	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs218970	chr7:10986944-10986945	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs551074723	chr7:10986972-10986973	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs60675058	chr7:10987009-10987010	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs189394878	chr7:10987031-10987032	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs553639169	chr7:10987036-10987037	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	22286061	CNVD
Non-small cell lung cancer	21829676	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Medulloblastoma	17653508	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	18194544	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Breast cancer	22522925	CNVD
Lung adenocarcinoma	21935476	CNVD
Gastric cancer	22014070	CNVD

Chromatin state (count:240 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:10981200-10989200	Weak transcription	HepG2	liver
2	chr7:10989200-10990600	Enhancers	HepG2	liver
3	chr7:10990600-10991800	Weak transcription	HepG2	liver
4	chr7:10991800-10992400	Enhancers	HepG2	liver
5	chr7:10992000-10993000	Enhancers	Stomach Mucosa	stomach
6	chr7:10992400-10995800	Weak transcription	HepG2	liver
7	chr7:10992800-10993600	Enhancers	GM12878-XiMat	blood
8	chr7:10995800-10996200	Active TSS	HepG2	liver
9	chr7:10998200-10999000	Weak transcription	Pancreas	Pancrea
10	chr7:10999000-10999400	ZNF genes & repeats	Pancreas	Pancrea
11	chr7:11004800-11005200	Enhancers	Primary T helper cells fromperipheralblood	blood
12	chr7:11004800-11005400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
13	chr7:11004800-11005400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
14	chr7:11004800-11005400	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
15	chr7:11004800-11005400	Enhancers	Primary T killer memory cells from peripheral blood	blood
16	chr7:11004800-11005600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
17	chr7:11004800-11005800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
18	chr7:11005000-11005400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
19	chr7:11005000-11005600	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
20	chr7:11005000-11005600	Enhancers	Dnd41	blood
21	chr7:11005400-11005800	Bivalent Enhancer	HepG2	liver
22	chr7:11005400-11012400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
23	chr7:11010600-11011000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr7:11010600-11011200	Enhancers	Dnd41	blood
25	chr7:11011000-11012800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr7:11011200-11012400	Weak transcription	Dnd41	blood
27	chr7:11012000-11012200	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr7:11012000-11012200	Enhancers	HepG2	liver
29	chr7:11012200-11012400	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr7:11012200-11012400	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
31	chr7:11012200-11012400	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr7:11012200-11012400	Enhancers	Hela-S3	cervix
33	chr7:11012200-11012400	Flanking Active TSS	HepG2	liver
34	chr7:11012200-11012600	Flanking Active TSS	A549	lung
35	chr7:11012200-11014400	Active TSS	ES-I3 Cell Line	embryonic stem cell
36	chr7:11012400-11012600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
37	chr7:11012400-11012600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr7:11012400-11012600	Enhancers	Breast Myoepithelial Primary Cells	Breast
39	chr7:11012400-11012600	Enhancers	Primary hematopoietic stem cells short term culture	blood
40	chr7:11012400-11012600	Enhancers	Primary T killer memory cells from peripheral blood	blood
41	chr7:11012400-11012600	Flanking Active TSS	Brain Anterior Caudate	brain
42	chr7:11012400-11012600	Enhancers	Brain Hippocampus Middle	brain
43	chr7:11012400-11012600	Enhancers	Pancreatic Islets	Pancreatic Islet
44	chr7:11012400-11012600	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
45	chr7:11012400-11012600	Enhancers	Rectal Mucosa Donor 31	rectum
46	chr7:11012400-11012800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
47	chr7:11012400-11012800	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr7:11012400-11012800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
49	chr7:11012400-11012800	Enhancers	Primary T helper cells fromperipheralblood	blood
50	chr7:11012400-11012800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood

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