Variant report

Variant	esv3370563
Chromosome Location	chr7:4775026-4779224
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:397)
CpG islands
(count:305)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:397 , 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	ARID3A	chr7:4778370-4778734	K562	blood:	n/a	n/a
2	ATF1	chr7:4778420-4779344	K562	blood:	n/a	n/a
3	ATF3	chr7:4778441-4778945	A549	lung:	n/a	n/a
4	ATF3	chr7:4778249-4778901	A549	lung:	n/a	n/a
5	ATF3	chr7:4778336-4778755	K562	blood:	n/a	n/a
6	BACH1	chr7:4778387-4779341	K562	blood:	n/a	n/a
7	BACH1	chr7:4778336-4778835	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL3	chr7:4778195-4779019	A549	lung:	n/a	chr7:4778390-4778398
9	BCL3	chr7:4776805-4777372	GM12878	blood:	n/a	n/a
10	BCL3	chr7:4776892-4777354	GM12878	blood:	n/a	n/a
11	BCL3	chr7:4778179-4779583	A549	lung:	n/a	chr7:4778390-4778398 chr7:4779359-4779372
12	BHLHE40	chr7:4779079-4779378	HepG2	liver:	n/a	n/a
13	BHLHE40	chr7:4778417-4779530	K562	blood:	n/a	n/a
14	CBX3	chr7:4778254-4779547	K562	blood:	n/a	n/a
15	CCNT2	chr7:4778316-4778985	K562	blood:	n/a	n/a
16	CEBPB	chr7:4777565-4777629	HepG2	liver:	n/a	n/a
17	CEBPB	chr7:4778260-4778991	A549	lung:	n/a	chr7:4778961-4778973
18	CEBPB	chr7:4778358-4778914	A549	lung:	n/a	n/a
19	CEBPB	chr7:4778282-4779088	K562	blood:	n/a	chr7:4778961-4778973
20	CEBPB	chr7:4777525-4779040	IMR90	lung:	n/a	chr7:4778961-4778973
21	CEBPB	chr7:4777587-4779035	A549	lung:	n/a	chr7:4778961-4778973
22	CEBPB	chr7:4777563-4779101	K562	blood:	n/a	chr7:4778961-4778973
23	CHD2	chr7:4778403-4778660	HepG2	liver:	n/a	n/a
24	CHD2	chr7:4778346-4778909	K562	blood:	n/a	n/a
25	CHD2	chr7:4779117-4779367	HepG2	liver:	n/a	n/a
26	CHD2	chr7:4779124-4779418	K562	blood:	n/a	n/a
27	CREB1	chr7:4778445-4778836	A549	lung:	n/a	n/a
28	CREB1	chr7:4778309-4778835	A549	lung:	n/a	n/a
29	CTCF	chr7:4778500-4778650	NB4	blood:	n/a	n/a
30	CTCF	chr7:4778583-4778640	GM12892	blood:	n/a	n/a
31	CTCF	chr7:4778520-4778670	HepG2	liver:	n/a	n/a
32	CTCF	chr7:4779220-4779370	WERI-Rb-1	eye:	n/a	n/a
33	CTCF	chr7:4778619-4778627	GM13977	blood:	n/a	n/a
34	CTCF	chr7:4778600-4778750	BJ	skin:	n/a	n/a
35	CTCF	chr7:4777075-4777138	MCF-7	breast:	n/a	n/a
36	CTCF	chr7:4779200-4779350	A549	lung:	n/a	n/a
37	CTCF	chr7:4778556-4778676	HepG2	liver:	n/a	n/a
38	CTCF	chr7:4777095-4777136	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr7:4778520-4778670	HMF	breast:	n/a	n/a
40	CTCF	chr7:4778520-4778670	RPTEC	kidney:	n/a	n/a
41	CTCF	chr7:4777035-4777220	GM19239	blood:	n/a	n/a
42	CTCF	chr7:4778480-4778630	HPAF	blood vessel:	n/a	n/a
43	CTCF	chr7:4778540-4778690	HRE	kidney:	n/a	n/a
44	CTCF	chr7:4778508-4778728	K562	blood:	n/a	n/a
45	CTCF	chr7:4778560-4778710	AG10803	skin:	n/a	n/a
46	CTCF	chr7:4778560-4778710	GM12865	blood:	n/a	n/a
47	CTCF	chr7:4779144-4779483	K562	blood:	n/a	n/a
48	CTCF	chr7:4778531-4778682	Fibrobl	skin:	n/a	n/a
49	CTCF	chr7:4778420-4778570	HFF-Myc	foreskin:	n/a	n/a
50	CTCF	chr7:4778552-4778622	Spleen_OC	spleen:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:4778908-4778958	AG04450	lung:	fetal
2	chr7:4778908-4778958	HPAEpiC	pulmonary alveolar:	n/a
3	chr7:4775247-4775297	GM12878	blood:	n/a
4	chr7:4775247-4775297	Hepatocyte	liver:	n/a
5	chr7:4775247-4775297	GM12892	blood:	n/a
6	chr7:4778908-4778958	AG04449	skin:	fetal
7	chr7:4775278-4775328	HNPCEpiC	eye:	n/a
8	chr7:4775278-4775328	T-47D	breast:	n/a
9	chr7:4775278-4775328	AG10803	skin:	n/a
10	chr7:4775247-4775297	U87	brain:	n/a
11	chr7:4778908-4778958	SK-N-MC	brain:	n/a
12	chr7:4775247-4775297	GM19239	blood:	n/a
13	chr7:4775278-4775328	NB4	blood:	n/a
14	chr7:4778908-4778958	RPTEC	kidney:	n/a
15	chr7:4775278-4775328	A549	lung:	n/a
16	chr7:4778881-4778931	HCF	heart:	n/a
17	chr7:4778908-4778958	NT2-D1	testis:	n/a
18	chr7:4778908-4778958	ovcar-3	ovarian:	n/a
19	chr7:4778908-4778958	PrEC	prostate:	n/a
20	chr7:4778839-4778889	AG10803	skin:	n/a
21	chr7:4778839-4778889	CMK	blood:	n/a
22	chr7:4775247-4775297	PrEC	prostate:	n/a
23	chr7:4778839-4778889	NHBE	bronchial:	n/a
24	chr7:4778839-4778889	ECC-1	luminal epithelium:	n/a
25	chr7:4778839-4778889	PrEC	prostate:	n/a
26	chr7:4775247-4775297	SAEC	small airway:	n/a
27	chr7:4778881-4778931	SAEC	small airway:	n/a
28	chr7:4778839-4778889	K562	blood:	n/a
29	chr7:4778908-4778958	AG09309	skin:	n/a
30	chr7:4778839-4778889	GM06990	blood:	n/a
31	chr7:4775247-4775297	HEK293	kidney:	embryo
32	chr7:4778881-4778931	PFSK-1	brain:	n/a
33	chr7:4778908-4778958	U87	brain:	n/a
34	chr7:4775247-4775297	MCF-7	breast:	n/a
35	chr7:4775278-4775328	AG04449	skin:	fetal
36	chr7:4775278-4775328	RPTEC	kidney:	n/a
37	chr7:4778908-4778958	MCF10A-Er-Src	breast:	n/a
38	chr7:4778908-4778958	Jurkat	blood:	n/a
39	chr7:4778839-4778889	H1-hESC	embryonic stem cell:	embryo
40	chr7:4775278-4775328	PrEC	prostate:	n/a
41	chr7:4778839-4778889	PANC-1	pancreas:	n/a
42	chr7:4775278-4775328	HIPEpiC	eye:	n/a
43	chr7:4775278-4775328	HRCEpiC	kidney:	n/a
44	chr7:4778839-4778889	HEK293	kidney:	embryo
45	chr7:4775247-4775297	SKMC	muscle:	n/a
46	chr7:4778839-4778889	AoSMC	blood vessel:	n/a
47	chr7:4778908-4778958	A549	lung:	n/a
48	chr7:4778881-4778931	HUVEC	blood vessel:	n/a
49	chr7:4778881-4778931	HRPEpiC	eye:	n/a
50	chr7:4778839-4778889	Hela-S3	cervix:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:4768370..4770170-chr7:4773458..4776418,2	K562	blood:
2	chr7:4763802..4765803-chr7:4775724..4778098,2	MCF-7	breast:
3	chr7:4718155..4726493-chr7:4775257..4787798,22	MCF-7	breast:
4	chr7:4771014..4776153-chr7:4776925..4780694,6	K562	blood:
5	chr7:4778391..4781100-chr7:4828582..4831115,2	K562	blood:
6	chr7:4721394..4723500-chr7:4773564..4775066,2	MCF-7	breast:
7	chr7:4777828..4782067-chr7:4812094..4815733,5	K562	blood:
8	chr7:4777402..4779328-chr7:4814233..4816172,2	K562	blood:
9	chr7:4776650..4779516-chr7:4815210..4817284,2	MCF-7	breast:
10	chr7:4738046..4740037-chr7:4772327..4775096,2	K562	blood:
11	chr7:4777042..4778807-chr7:4793981..4795930,2	MCF-7	breast:
12	chr7:4679860..4681544-chr7:4777354..4780296,2	K562	blood:

No data

Variant related genes	Relation type
FOXK1	TF binding region
FOXK1	CpG island
ENSG00000242802	chromatin interactions
ENSG00000164916	chromatin interactions

Extended variants
information (count: 231 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:231 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532373511	chr7:4775026-4775027	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs367548819	chr7:4775048-4775049	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs6977882	chr7:4775049-4775050	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs56911085	chr7:4775066-4775067	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs148385281	chr7:4775105-4775106	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs140434729	chr7:4775135-4775136	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs561181260	chr7:4775142-4775143	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs528465055	chr7:4775155-4775156	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs547018257	chr7:4775158-4775159	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs187786433	chr7:4775175-4775176	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs532627792	chr7:4775180-4775181	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs550838709	chr7:4775248-4775249	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs577429023	chr7:4775263-4775264	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs536467033	chr7:4775267-4775268	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs56030601	chr7:4775270-4775271	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs150408343	chr7:4775279-4775280	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs566829518	chr7:4775284-4775285	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs534280113	chr7:4775293-4775294	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs138278591	chr7:4775308-4775309	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs577612567	chr7:4775323-4775324	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs535095609	chr7:4775331-4775332	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs545066719	chr7:4775366-4775367	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs191453645	chr7:4775367-4775368	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs575475726	chr7:4775381-4775382	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs542863916	chr7:4775387-4775388	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs112443938	chr7:4775391-4775392	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs76552106	chr7:4775397-4775398	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs540570659	chr7:4775411-4775412	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs146106677	chr7:4775429-4775430	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs115778992	chr7:4775466-4775467	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs10271191	chr7:4775470-4775471	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs10260874	chr7:4775475-4775476	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs75547826	chr7:4775491-4775492	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs10257680	chr7:4775507-4775508	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs566766229	chr7:4775649-4775650	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs558499850	chr7:4775684-4775685	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs111820455	chr7:4775693-4775694	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs552622995	chr7:4775707-4775708	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs576624702	chr7:4775711-4775712	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs545140210	chr7:4775729-4775730	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs141785678	chr7:4775826-4775827	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs563402032	chr7:4775850-4775851	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs188266703	chr7:4775856-4775857	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs144590577	chr7:4775924-4775925	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs554792782	chr7:4775930-4775931	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs573119981	chr7:4775952-4775953	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs575235416	chr7:4775967-4775968	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs542628195	chr7:4775974-4775975	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs148488308	chr7:4776001-4776002	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs565051586	chr7:4776015-4776016	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	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
Developmental delay	21147756	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Urothelial carcinoma	21177765	CNVD
Glioblastoma multiforme	21525872	CNVD
Bladder cancer	21909424	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21045282	CNVD
Disorders of sex development	21048976	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Cancer	20164919	CNVD
Gastric cancer	22014070	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:450 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:4756400-4776800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr7:4757200-4778800	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr7:4765400-4778200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr7:4765600-4777600	Strong transcription	Fetal Intestine Small	intestine
5	chr7:4765600-4778200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr7:4765600-4778200	Weak transcription	Aorta	Aorta
7	chr7:4765600-4778200	Weak transcription	Ovary	ovary
8	chr7:4765600-4778400	Weak transcription	Brain Germinal Matrix	brain
9	chr7:4765600-4783200	Weak transcription	Fetal Brain Male	brain
10	chr7:4765600-4784000	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr7:4765800-4778200	Weak transcription	Osteobl	bone
12	chr7:4765800-4778400	Weak transcription	Fetal Kidney	kidney
13	chr7:4765800-4782400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr7:4766000-4778000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr7:4766000-4778000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr7:4766000-4778000	Weak transcription	NHDF-Ad	bronchial
17	chr7:4766000-4778200	Weak transcription	Fetal Brain Female	brain
18	chr7:4766000-4778200	Weak transcription	HSMM	muscle
19	chr7:4766000-4778800	Weak transcription	Pancreatic Islets	Pancreatic Islet
20	chr7:4766000-4783600	Weak transcription	HMEC	breast
21	chr7:4766200-4778200	Weak transcription	Stomach Mucosa	stomach
22	chr7:4766400-4778000	Weak transcription	HUVEC	blood vessel
23	chr7:4766600-4778000	Weak transcription	Liver	Liver
24	chr7:4766800-4776400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr7:4767200-4775200	Strong transcription	Fetal Intestine Large	intestine
26	chr7:4767800-4775600	Strong transcription	Cortex derived primary cultured neurospheres	brain
27	chr7:4768000-4781600	Weak transcription	Rectal Mucosa Donor 31	rectum
28	chr7:4768200-4778200	Weak transcription	Rectal Smooth Muscle	rectum
29	chr7:4768400-4778200	Weak transcription	Duodenum Mucosa	Duodenum
30	chr7:4768800-4777800	Weak transcription	Muscle Satellite Cultured Cells	--
31	chr7:4768800-4778000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr7:4770200-4777000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr7:4770200-4777000	Weak transcription	Pancreas	Pancrea
34	chr7:4770200-4778200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr7:4770400-4777000	Weak transcription	HUES6 Cell Line	embryonic stem cell
36	chr7:4770400-4778200	Weak transcription	Gastric	stomach
37	chr7:4770800-4776600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr7:4771000-4777000	Weak transcription	NHLF	lung
39	chr7:4771000-4777400	Strong transcription	Fetal Stomach	stomach
40	chr7:4771000-4778200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
41	chr7:4771000-4778200	Weak transcription	Colon Smooth Muscle	Colon
42	chr7:4772000-4777200	Weak transcription	Placenta	Placenta
43	chr7:4772200-4775400	Enhancers	Brain Substantia Nigra	brain
44	chr7:4772400-4776400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr7:4773000-4775400	Enhancers	Lung	lung
46	chr7:4773000-4775400	Enhancers	Right Ventricle	heart
47	chr7:4773200-4775200	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
48	chr7:4773200-4775400	Enhancers	Brain Cingulate Gyrus	brain
49	chr7:4773200-4776600	Weak transcription	Primary B cells from cord blood	blood
50	chr7:4773200-4776800	Weak transcription	GM12878-XiMat	blood

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