Variant report

Variant	nsv830944
Chromosome Location	chr7:33389892-33549882
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:962)
CpG islands
(count:305)
Chromatin interactive
region (count:24)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:962 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:33397641-33397646	K562	blood:	n/a	n/a
2	ATF2	chr7:33511318-33511802	GM12878	blood:	n/a	n/a
3	BACH1	chr7:33492541-33492768	K562	blood:	n/a	n/a
4	BACH1	chr7:33495168-33495210	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr7:33492456-33492655	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr7:33511374-33511766	GM12878	blood:	n/a	chr7:33511606-33511615
7	BATF	chr7:33463182-33463442	GM12878	blood:	n/a	n/a
8	BATF	chr7:33517312-33517626	GM12878	blood:	n/a	n/a
9	BATF	chr7:33517332-33517647	GM12878	blood:	n/a	n/a
10	BATF	chr7:33511401-33511731	GM12878	blood:	n/a	chr7:33511606-33511615
11	BCL11A	chr7:33517380-33517593	GM12878	blood:	n/a	chr7:33517559-33517568
12	BCL11A	chr7:33511382-33511772	GM12878	blood:	n/a	n/a
13	BCL3	chr7:33511380-33511806	GM12878	blood:	n/a	n/a
14	BHLHE40	chr7:33511602-33511635	GM12878	blood:	n/a	n/a
15	BHLHE40	chr7:33527676-33527991	GM12878	blood:	n/a	n/a
16	CEBPB	chr7:33489436-33489697	IMR90	lung:	n/a	chr7:33489558-33489569
17	CEBPB	chr7:33455450-33455468	HepG2	liver:	n/a	n/a
18	CEBPB	chr7:33400672-33400966	IMR90	lung:	n/a	n/a
19	CEBPB	chr7:33489448-33489725	HepG2	liver:	n/a	chr7:33489558-33489569
20	CEBPB	chr7:33475790-33476059	HepG2	liver:	n/a	chr7:33475910-33475921
21	CEBPB	chr7:33397437-33397913	MCF-7	breast:	n/a	n/a
22	CEBPB	chr7:33514368-33514561	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr7:33534831-33535155	IMR90	lung:	n/a	chr7:33534996-33535009 chr7:33534996-33535009 chr7:33534998-33535009
24	CEBPB	chr7:33489521-33489594	Hela-S3	cervix:	n/a	chr7:33489558-33489569
25	CEBPB	chr7:33391358-33391654	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr7:33468209-33468226	A549	lung:	n/a	n/a
27	CEBPB	chr7:33400743-33400980	HepG2	liver:	n/a	n/a
28	CEBPB	chr7:33532292-33532456	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr7:33514465-33514752	MCF-7	breast:	n/a	n/a
30	CEBPB	chr7:33495619-33495622	A549	lung:	n/a	n/a
31	CEBPB	chr7:33455461-33455617	IMR90	lung:	n/a	n/a
32	CEBPB	chr7:33431614-33431774	HepG2	liver:	n/a	chr7:33431668-33431677 chr7:33431667-33431678 chr7:33431668-33431677 chr7:33431668-33431677 chr7:33431666-33431677 chr7:33431668-33431677 chr7:33431666-33431679
33	CEBPB	chr7:33485981-33486050	HepG2	liver:	n/a	chr7:33485988-33486001 chr7:33485989-33486000
34	CEBPB	chr7:33461052-33461367	IMR90	lung:	n/a	chr7:33461216-33461227
35	CEBPB	chr7:33534892-33535147	Hela-S3	cervix:	n/a	chr7:33534996-33535009 chr7:33534996-33535009 chr7:33534998-33535009
36	CEBPB	chr7:33498960-33499280	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr7:33475778-33476051	A549	lung:	n/a	chr7:33475910-33475921
38	CEBPB	chr7:33400718-33400968	A549	lung:	n/a	n/a
39	CEBPB	chr7:33534832-33535130	H1-hESC	embryonic stem cell:	n/a	chr7:33534996-33535009 chr7:33534996-33535009 chr7:33534998-33535009
40	CHD1	chr7:33392842-33393067	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD1	chr7:33391419-33391874	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD1	chr7:33502039-33502212	GM12878	blood:	n/a	n/a
43	CHD2	chr7:33517472-33517556	GM12878	blood:	n/a	n/a
44	CHD2	chr7:33495257-33495273	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD2	chr7:33391450-33391725	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD2	chr7:33502817-33503090	GM12878	blood:	n/a	n/a
47	CHD2	chr7:33531995-33532392	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr7:33499188-33499386	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr7:33463360-33463510	HPF	lung:	n/a	chr7:33463417-33463426 chr7:33463416-33463437 chr7:33463414-33463432
50	CTCF	chr7:33463320-33463470	GM12871	blood:	n/a	chr7:33463417-33463426 chr7:33463416-33463437 chr7:33463414-33463432

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:33462512-33462562	SK-N-MC	brain:	n/a
2	chr7:33457940-33457990	MCF10A-Er-Src	breast:	n/a
3	chr7:33457940-33457990	SK-N-SH	brain:	n/a
4	chr7:33534876-33534926	AoSMC	blood vessel:	n/a
5	chr7:33534876-33534926	SK-N-SH_RA	brain:	n/a
6	chr7:33534876-33534926	BJ	skin:	n/a
7	chr7:33462512-33462562	HCM	heart:	n/a
8	chr7:33534876-33534926	ProgFib	skin:	n/a
9	chr7:33533728-33533778	SAEC	small airway:	n/a
10	chr7:33457940-33457990	HNPCEpiC	eye:	n/a
11	chr7:33533728-33533778	HCPEpiC	choroid plexus:	n/a
12	chr7:33457940-33457990	AG10803	skin:	n/a
13	chr7:33534876-33534926	T-47D	breast:	n/a
14	chr7:33534876-33534926	SK-N-SH	brain:	n/a
15	chr7:33534876-33534926	HRE	kidney:	n/a
16	chr7:33389885-33389935	SK-N-SH_RA	brain:	n/a
17	chr7:33457940-33457990	H1-hESC	embryonic stem cell:	embryo
18	chr7:33534876-33534926	NT2-D1	testis:	n/a
19	chr7:33533728-33533778	K562	blood:	n/a
20	chr7:33389885-33389935	HepG2	liver:	n/a
21	chr7:33457940-33457990	GM12878	blood:	n/a
22	chr7:33534876-33534926	HCT-116	colon:	n/a
23	chr7:33389885-33389935	NH-A	brain:	n/a
24	chr7:33533728-33533778	Caco-2	colon:	n/a
25	chr7:33457940-33457990	MCF-7	breast:	n/a
26	chr7:33533728-33533778	AG04450	lung:	fetal
27	chr7:33389885-33389935	AG10803	skin:	n/a
28	chr7:33389885-33389935	HL-60	blood:	n/a
29	chr7:33457940-33457990	PFSK-1	brain:	n/a
30	chr7:33533728-33533778	PFSK-1	brain:	n/a
31	chr7:33533728-33533778	ECC-1	luminal epithelium:	n/a
32	chr7:33533728-33533778	BJ	skin:	n/a
33	chr7:33534876-33534926	HAEpiC	amniotic membrane:	n/a
34	chr7:33389885-33389935	RPTEC	kidney:	n/a
35	chr7:33533728-33533778	HAEpiC	amniotic membrane:	n/a
36	chr7:33534876-33534926	MCF-7	breast:	n/a
37	chr7:33457940-33457990	HRE	kidney:	n/a
38	chr7:33462512-33462562	RPTEC	kidney:	n/a
39	chr7:33389885-33389935	AG04449	skin:	fetal
40	chr7:33533728-33533778	GM12892	blood:	n/a
41	chr7:33389885-33389935	HPAEpiC	pulmonary alveolar:	n/a
42	chr7:33533728-33533778	U87	brain:	n/a
43	chr7:33533728-33533778	IMR90	lung:	fetal
44	chr7:33462512-33462562	SAEC	small airway:	n/a
45	chr7:33533728-33533778	MCF10A-Er-Src	breast:	n/a
46	chr7:33462512-33462562	HL-60	blood:	n/a
47	chr7:33457940-33457990	HRCEpiC	kidney:	n/a
48	chr7:33457940-33457990	HAEpiC	amniotic membrane:	n/a
49	chr7:33389885-33389935	HRE	kidney:	n/a
50	chr7:33533728-33533778	Hela-S3	cervix:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:4047787..4048628-chr7:33396481..33397227,2	MCF-7	breast:
2	chr7:33417630..33419879-chr7:33421037..33423794,2	K562	blood:
3	chr7:33373710..33374867-chr7:33498631..33499702,4	MCF-7	breast:
4	chr7:33407715..33410648-chr7:33411444..33414144,2	K562	blood:
5	chr7:33448405..33450851-chr7:33456089..33457716,2	MCF-7	breast:
6	chr10:118270037..118270892-chr7:33545417..33545952,2	MCF-7	breast:
7	chr7:33499224..33499840-chr7:33756036..33756556,2	MCF-7	breast:
8	chr7:33417630..33419879-chr7:33421037..33423794,2	K562	blood:
9	chr7:33381826..33383987-chr7:33388092..33389898,2	MCF-7	breast:
10	chr7:33535469..33537729-chr7:33538223..33540733,2	MCF-7	breast:
11	chr7:33387307..33390007-chr7:33559029..33560942,2	K562	blood:
12	chr7:33528273..33530011-chr7:33531942..33534154,2	K562	blood:
13	chr7:33535469..33537729-chr7:33538223..33540733,2	MCF-7	breast:
14	chr7:33480819..33483351-chr7:33485248..33487940,2	K562	blood:
15	chr7:33225084..33225594-chr7:33499029..33499648,2	MCF-7	breast:
16	chr7:33438887..33440911-chr7:33449255..33451707,2	K562	blood:
17	chr7:33438887..33440911-chr7:33449255..33451707,2	K562	blood:
18	chr7:33480819..33483351-chr7:33485248..33487940,2	K562	blood:
19	chr7:33498720..33499554-chr7:33783613..33784456,2	MCF-7	breast:
20	chr7:33282661..33283550-chr7:33499199..33499750,2	MCF-7	breast:
21	chr7:33462937..33463514-chr7:33783854..33784554,2	MCF-7	breast:
22	chr7:33528273..33530011-chr7:33531942..33534154,2	K562	blood:
23	chr7:33407715..33410648-chr7:33411444..33414144,2	K562	blood:
24	chr7:33448405..33450851-chr7:33456089..33457716,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AVL9-4	chr7:33419576-33420498	NONHSAT120025

No data

Variant related genes	Relation type
BBS9	TF binding region
ENSG00000238090	TF binding region
BBS9	CpG island
ENSG00000238090	CpG island
ENSG00000122507	chromatin interactions
ENSG00000238090	chromatin interactions

Extended variants
information (count: 5781 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:5781 , 50 per page) page: 1 2 3 4 5 6 7 ... 116

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs542583923	chr7:33389948-33389949	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs79991797	chr7:33389977-33389978	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs192622312	chr7:33390042-33390043	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs138791472	chr7:33390125-33390126	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs182165337	chr7:33390194-33390195	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs576508010	chr7:33390205-33390206	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs564568345	chr7:33390226-33390227	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs557630028	chr7:33390227-33390228	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs76745139	chr7:33390234-33390235	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs186805945	chr7:33390262-33390263	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs568404748	chr7:33390329-33390330	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs577695775	chr7:33390396-33390397	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs547243216	chr7:33390424-33390425	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs111340925	chr7:33390503-33390504	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs117673131	chr7:33390549-33390550	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs78352573	chr7:33390594-33390595	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs141974885	chr7:33390620-33390621	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs146325498	chr7:33390677-33390678	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs56655388	chr7:33390702-33390703	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs555332121	chr7:33390728-33390729	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs573637947	chr7:33390755-33390756	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs113611210	chr7:33390771-33390772	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs534602614	chr7:33390789-33390790	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs554475549	chr7:33390801-33390802	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs200850911	chr7:33390862-33390863	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs375968976	chr7:33390864-33390865	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs369146555	chr7:33390884-33390885	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs139303948	chr7:33390885-33390886	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs546359350	chr7:33390943-33390944	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs561227158	chr7:33390959-33390960	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs200032502	chr7:33390979-33390980	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs148529246	chr7:33391013-33391014	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs543512918	chr7:33391059-33391060	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs35557465	chr7:33391089-33391090	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs76983967	chr7:33391094-33391095	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs547403773	chr7:33391129-33391130	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs192562413	chr7:33391131-33391132	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs6955645	chr7:33391139-33391140	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs35054346	chr7:33391173-33391174	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs367751412	chr7:33391179-33391180	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs569791059	chr7:33391188-33391189	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs574514229	chr7:33391276-33391277	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs184853206	chr7:33391283-33391284	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs150665588	chr7:33391284-33391285	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs79030728	chr7:33391324-33391325	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs538739333	chr7:33391334-33391335	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs534563624	chr7:33391362-33391363	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs551843444	chr7:33391425-33391426	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs118022457	chr7:33391430-33391431	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs572776664	chr7:33391510-33391511	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

Disease	PMID	Source
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
Melanoma	18172304	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
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
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Non-syndromic sensorineural hearing loss	22570644	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21364760	CNVD
Lung adenocarcinoma	21935476	CNVD
Colorectal cancer	21645411	CNVD
Myelofibrosis	22110671	CNVD
Autism	22241247	CNVD
Williams-beuren syndrome	18553513	CNVD
Breast cancer	22522925	CNVD
Aortic dissecting aneurysms	22263138	CNVD

Chromatin state (count:996 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:33355200-33419600	Weak transcription	Primary T cells from cord blood	blood
2	chr7:33362200-33404400	Weak transcription	Ovary	ovary
3	chr7:33362200-33404800	Weak transcription	Fetal Lung	lung
4	chr7:33370600-33396200	Weak transcription	Adipose Nuclei	Adipose
5	chr7:33375800-33399200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr7:33377600-33404800	Weak transcription	Left Ventricle	heart
7	chr7:33377800-33392600	Weak transcription	Primary B cells from peripheral blood	blood
8	chr7:33378000-33392800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr7:33378200-33404400	Weak transcription	Aorta	Aorta
10	chr7:33379600-33391800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
11	chr7:33380000-33404400	Weak transcription	Duodenum Smooth Muscle	Duodenum
12	chr7:33380200-33393800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr7:33380400-33393200	Weak transcription	Primary B cells from cord blood	blood
14	chr7:33380400-33393400	Weak transcription	Fetal Stomach	stomach
15	chr7:33380600-33404800	Weak transcription	Stomach Smooth Muscle	stomach
16	chr7:33381400-33407200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
17	chr7:33384000-33425400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
18	chr7:33384200-33395800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr7:33384800-33391000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr7:33385800-33407000	Weak transcription	Primary T helper cells fromperipheralblood	blood
21	chr7:33386000-33394000	Weak transcription	Fetal Kidney	kidney
22	chr7:33386000-33407400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr7:33386400-33408200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr7:33386600-33393200	Weak transcription	Psoas Muscle	Psoas
25	chr7:33387000-33425200	Weak transcription	Primary T cells fromperipheralblood	blood
26	chr7:33388800-33390800	Strong transcription	Colon Smooth Muscle	Colon
27	chr7:33388800-33404800	Weak transcription	Lung	lung
28	chr7:33389000-33437400	Weak transcription	Liver	Liver
29	chr7:33390200-33391400	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr7:33390200-33391600	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr7:33390400-33390600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr7:33390400-33391400	Enhancers	H9 Cell Line	embryonic stem cell
33	chr7:33390400-33392800	Weak transcription	Sigmoid Colon	Sigmoid Colon
34	chr7:33390800-33394600	Weak transcription	Colon Smooth Muscle	Colon
35	chr7:33391000-33391200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
36	chr7:33391000-33391400	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr7:33391000-33391600	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr7:33391200-33391600	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr7:33391200-33391600	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr7:33391200-33397400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
41	chr7:33391400-33391800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr7:33391400-33391800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr7:33391400-33391800	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr7:33391400-33392800	Active TSS	H1 Cell Line	embryonic stem cell
45	chr7:33391400-33394000	Active TSS	H9 Cell Line	embryonic stem cell
46	chr7:33391400-33395400	Active TSS	HUES6 Cell Line	embryonic stem cell
47	chr7:33391400-33396600	Active TSS	ES-I3 Cell Line	embryonic stem cell
48	chr7:33391600-33391800	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
49	chr7:33391600-33391800	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
50	chr7:33391600-33391800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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