Variant report

Variant	nsv1030157
Chromosome Location	chr7:4272488-4311316
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:4275147-4275340	HepG2	liver:	n/a	n/a
2	CTCF	chr7:4281656-4281712	HepG2	liver:	n/a	chr7:4281691-4281704 chr7:4281691-4281700
3	CTCF	chr7:4281663-4281709	MCF-7	breast:	n/a	chr7:4281691-4281704 chr7:4281691-4281700
4	CTCF	chr7:4281590-4281763	MCF-7	breast:	n/a	chr7:4281691-4281704 chr7:4281691-4281700
5	CTCF	chr7:4281580-4281730	K562	blood:	n/a	chr7:4281691-4281704 chr7:4281691-4281700
6	CTCF	chr7:4299858-4299930	Lung_OC	lung:	n/a	n/a
7	CTCF	chr7:4281560-4281710	HepG2	liver:	n/a	chr7:4281691-4281704 chr7:4281571-4281580 chr7:4281691-4281700
8	CTCF	chr7:4281680-4281830	NHEK	skin:	n/a	chr7:4281691-4281704 chr7:4281691-4281700
9	CTCF	chr7:4281620-4281770	HEEpiC	esophagus:	n/a	chr7:4281691-4281704 chr7:4281691-4281700
10	CTCF	chr7:4286720-4286870	MCF-7	breast:	n/a	n/a
11	CTCF	chr7:4281580-4281730	HEK293	kidney:	n/a	chr7:4281691-4281704 chr7:4281691-4281700
12	CTCF	chr7:4281532-4281817	H1-hESC	embryonic stem cell:	n/a	chr7:4281691-4281704 chr7:4281571-4281580 chr7:4281691-4281700
13	CTCF	chr7:4281647-4281726	Gliobla	brain:	n/a	chr7:4281691-4281704 chr7:4281691-4281700
14	CTCF	chr7:4281560-4281710	WERI-Rb-1	eye:	n/a	chr7:4281691-4281704 chr7:4281571-4281580 chr7:4281691-4281700
15	CTCF	chr7:4285420-4285570	MCF-7	breast:	n/a	n/a
16	CTCF	chr7:4281625-4281749	K562	blood:	n/a	chr7:4281691-4281704 chr7:4281691-4281700
17	CTCF	chr7:4281620-4281770	Hela-S3	cervix:	n/a	chr7:4281691-4281704 chr7:4281691-4281700
18	CTCF	chr7:4281599-4281776	MCF-7	breast:	n/a	chr7:4281691-4281704 chr7:4281691-4281700
19	CTCF	chr7:4281548-4281912	K562	blood:	n/a	chr7:4281691-4281704 chr7:4281571-4281580 chr7:4281691-4281700
20	CTCF	chr7:4281560-4281710	SK-N-SH_RA	brain:	n/a	chr7:4281691-4281704 chr7:4281571-4281580 chr7:4281691-4281700
21	CTCF	chr7:4301464-4301518	H1-hESC	embryonic stem cell:	n/a	chr7:4301485-4301498 chr7:4301485-4301503 chr7:4301488-4301497
22	CTCF	chr7:4281600-4281750	MCF-7	breast:	n/a	chr7:4281691-4281704 chr7:4281691-4281700
23	CTCF	chr7:4281553-4281818	K562	blood:	n/a	chr7:4281691-4281704 chr7:4281571-4281580 chr7:4281691-4281700
24	CTCF	chr7:4281600-4281750	HCFaa	heart:	n/a	chr7:4281691-4281704 chr7:4281691-4281700
25	CTCF	chr7:4281626-4281742	MCF-7	breast:	n/a	chr7:4281691-4281704 chr7:4281691-4281700
26	CTCF	chr7:4281580-4281730	WERI-Rb-1	eye:	n/a	chr7:4281691-4281704 chr7:4281691-4281700
27	CTCF	chr7:4281666-4281715	A549	lung:	n/a	chr7:4281691-4281704 chr7:4281691-4281700
28	CTCF	chr7:4281632-4281724	MCF-7	breast:	n/a	chr7:4281691-4281704 chr7:4281691-4281700
29	CTCF	chr7:4281471-4281882	H1-hESC	embryonic stem cell:	n/a	chr7:4281691-4281704 chr7:4281571-4281580 chr7:4281691-4281700
30	CTCF	chr7:4281640-4281790	K562	blood:	n/a	chr7:4281691-4281704 chr7:4281691-4281700
31	CTCF	chr7:4281680-4281830	MCF-7	breast:	n/a	chr7:4281691-4281704 chr7:4281691-4281700
32	CTCF	chr7:4297920-4298070	MCF-7	breast:	n/a	n/a
33	CTCF	chr7:4281640-4281790	HRE	kidney:	n/a	chr7:4281691-4281704 chr7:4281691-4281700
34	CTCF	chr7:4281476-4281863	H1-hESC	embryonic stem cell:	n/a	chr7:4281691-4281704 chr7:4281571-4281580 chr7:4281691-4281700
35	CTCF	chr7:4286860-4287010	MCF-7	breast:	n/a	chr7:4286902-4286910
36	CTCF	chr7:4281640-4281790	SK-N-SH_RA	brain:	n/a	chr7:4281691-4281704 chr7:4281691-4281700
37	CTCF	chr7:4281620-4281770	HCT-116	colon:	n/a	chr7:4281691-4281704 chr7:4281691-4281700
38	CTCF	chr7:4281549-4281830	K562	blood:	n/a	chr7:4281691-4281704 chr7:4281571-4281580 chr7:4281691-4281700
39	CTCF	chr7:4281595-4281755	K562	blood:	n/a	chr7:4281691-4281704 chr7:4281691-4281700
40	CTCF	chr7:4281560-4281710	NB4	blood:	n/a	chr7:4281691-4281704 chr7:4281571-4281580 chr7:4281691-4281700
41	CTCF	chr7:4281640-4281790	HCT-116	colon:	n/a	chr7:4281691-4281704 chr7:4281691-4281700
42	CTCF	chr7:4281640-4281790	HRPEpiC	eye:	n/a	chr7:4281691-4281704 chr7:4281691-4281700
43	CTCF	chr7:4281673-4281707	Hela-S3	cervix:	n/a	chr7:4281691-4281704 chr7:4281691-4281700
44	CTCF	chr7:4281440-4281590	A549	lung:	n/a	chr7:4281571-4281580
45	CTCF	chr7:4281660-4281810	A549	lung:	n/a	chr7:4281691-4281704 chr7:4281691-4281700
46	E2F6	chr7:4297335-4297725	H1-hESC	embryonic stem cell:	n/a	n/a
47	E2F6	chr7:4304564-4304945	H1-hESC	embryonic stem cell:	n/a	chr7:4304738-4304750
48	E2F6	chr7:4297451-4297624	K562	blood:	n/a	n/a
49	E2F6	chr7:4297304-4297796	H1-hESC	embryonic stem cell:	n/a	n/a
50	E2F6	chr7:4304496-4304988	H1-hESC	embryonic stem cell:	n/a	chr7:4304738-4304750

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:4275962-4276012	ovcar-3	ovarian:	n/a
2	chr7:4300182-4300232	HIPEpiC	eye:	n/a
3	chr7:4309035-4309085	PFSK-1	brain:	n/a
4	chr7:4275962-4276012	ovcar-3	ovarian:	n/a
5	chr7:4300182-4300232	HIPEpiC	eye:	n/a
6	chr7:4309035-4309085	PFSK-1	brain:	n/a
7	chr7:4304846-4304896	HIPEpiC	eye:	n/a
8	chr7:4309035-4309085	AG04449	skin:	fetal
9	chr7:4308120-4308170	HMEC	breast:	n/a
10	chr7:4303790-4303840	HEK293	kidney:	embryo
11	chr7:4277473-4277523	HL-60	blood:	n/a
12	chr7:4308739-4308789	NT2-D1	testis:	n/a
13	chr7:4303109-4303159	NHDF-neo	bronchial:	n/a
14	chr7:4301346-4301396	NHBE	bronchial:	n/a
15	chr7:4302246-4302296	RPTEC	kidney:	n/a
16	chr7:4287215-4287265	HCT-116	colon:	n/a
17	chr7:4304397-4304447	HEEpiC	esophagus:	n/a
18	chr7:4305535-4305585	HCM	heart:	n/a
19	chr7:4304397-4304447	T-47D	breast:	n/a
20	chr7:4299646-4299696	HEK293	kidney:	embryo
21	chr7:4304779-4304829	T-47D	breast:	n/a
22	chr7:4303790-4303840	K562	blood:	n/a
23	chr7:4305042-4305092	PrEC	prostate:	n/a
24	chr7:4303790-4303840	GM12878	blood:	n/a
25	chr7:4308166-4308216	HCT-116	colon:	n/a
26	chr7:4308120-4308170	CMK	blood:	n/a
27	chr7:4308327-4308377	HIPEpiC	eye:	n/a
28	chr7:4308449-4308499	HCF	heart:	n/a
29	chr7:4300845-4300895	AG09319	gingival:	n/a
30	chr7:4275784-4275834	HEK293	kidney:	embryo
31	chr7:4300306-4300356	AG04450	lung:	fetal
32	chr7:4304397-4304447	HCPEpiC	choroid plexus:	n/a
33	chr7:4307490-4307540	AG10803	skin:	n/a
34	chr7:4287215-4287265	AG04450	lung:	fetal
35	chr7:4307490-4307540	HCF	heart:	n/a
36	chr7:4307490-4307540	HIPEpiC	eye:	n/a
37	chr7:4303193-4303243	HCT-116	colon:	n/a
38	chr7:4303109-4303159	ProgFib	skin:	n/a
39	chr7:4308209-4308259	GM12878	blood:	n/a
40	chr7:4301346-4301396	AoSMC	blood vessel:	n/a
41	chr7:4276204-4276254	HRE	kidney:	n/a
42	chr7:4300306-4300356	AG09309	skin:	n/a
43	chr7:4307433-4307483	PANC-1	pancreas:	n/a
44	chr7:4275634-4275684	BJ	skin:	n/a
45	chr7:4300306-4300356	HEK293	kidney:	embryo
46	chr7:4303109-4303159	SKMC	muscle:	n/a
47	chr7:4303165-4303215	HCT-116	colon:	n/a
48	chr7:4275962-4276012	AG09309	skin:	n/a
49	chr7:4302246-4302296	HCM	heart:	n/a
50	chr7:4276220-4276270	NHBE	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:4285802..4287439-chr7:4291050..4292753,2	MCF-7	breast:
2	chr7:4302968..4305028-chr7:4309435..4311444,2	MCF-7	breast:
3	chr7:4266434..4268284-chr7:4284245..4288090,3	MCF-7	breast:
4	chr7:4274876..4277578-chr7:4279083..4281112,2	K562	blood:
5	chr7:4306283..4308245-chr7:4322606..4324838,2	MCF-7	breast:
6	chr7:4277127..4279209-chr7:4282111..4283928,2	MCF-7	breast:
7	chr7:4225105..4227175-chr7:4279360..4281841,2	MCF-7	breast:
8	chr7:4287888..4289875-chr7:4302608..4305550,2	MCF-7	breast:
9	chr7:4280752..4283162-chr7:4283913..4286565,5	MCF-7	breast:
10	chr7:4280752..4283162-chr7:4283913..4286565,5	MCF-7	breast:
11	chr7:4281480..4283823-chr7:4284575..4286412,2	MCF-7	breast:
12	chr7:4285802..4287439-chr7:4291050..4292753,2	MCF-7	breast:
13	chr7:4309076..4311036-chr7:4311322..4313505,2	MCF-7	breast:
14	chr7:4274876..4277578-chr7:4279083..4281112,2	K562	blood:
15	chr7:4265084..4267850-chr7:4273909..4275894,2	K562	blood:
16	chr7:4277127..4279209-chr7:4282111..4283928,2	MCF-7	breast:
17	chr7:4287888..4289875-chr7:4302608..4305550,2	MCF-7	breast:
18	chr7:4309758..4311351-chr7:4312992..4314606,2	K562	blood:
19	chr7:4281480..4283823-chr7:4284575..4286412,2	MCF-7	breast:
20	chr7:4302968..4305028-chr7:4309435..4311444,2	MCF-7	breast:

Variant related genes	Relation type
SDK1	TF binding region
SDK1	CpG island
ENSG00000146555	chromatin interactions

Extended variants
information (count: 2324 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:2324 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs631530	chr7:4272488-4272489	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs141148258	chr7:4272490-4272491	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs550567968	chr7:4272495-4272496	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs570405896	chr7:4272498-4272499	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs575477987	chr7:4272514-4272515	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs528630950	chr7:4272522-4272523	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs144990971	chr7:4272546-4272547	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs559195086	chr7:4272547-4272548	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs566292432	chr7:4272559-4272560	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs534844384	chr7:4272565-4272566	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs181424152	chr7:4272586-4272587	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs4723516	chr7:4272587-4272588	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs543529609	chr7:4272593-4272594	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs545795204	chr7:4272604-4272605	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs577152259	chr7:4272619-4272620	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs545916998	chr7:4272624-4272625	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs559594818	chr7:4272649-4272650	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs78176663	chr7:4272652-4272653	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs564410540	chr7:4272674-4272675	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs531897013	chr7:4272675-4272676	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs2880458	chr7:4272685-4272686	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs561885985	chr7:4272695-4272696	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs543589360	chr7:4272709-4272710	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs185709268	chr7:4272725-4272726	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs550635722	chr7:4272730-4272731	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs570496002	chr7:4272734-4272735	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs532940269	chr7:4272777-4272778	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs562192095	chr7:4272803-4272804	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs113154539	chr7:4272804-4272805	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs566324517	chr7:4272807-4272808	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs535004608	chr7:4272812-4272813	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs114244421	chr7:4272834-4272835	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs373002433	chr7:4272840-4272841	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs202027111	chr7:4272843-4272844	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs375631216	chr7:4272845-4272846	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs374780395	chr7:4272851-4272852	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs367585225	chr7:4272865-4272866	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs372247216	chr7:4272866-4272867	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs577312842	chr7:4272868-4272869	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs375715373	chr7:4272880-4272881	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs369928102	chr7:4272881-4272882	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs544749299	chr7:4272884-4272885	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs138370726	chr7:4272890-4272891	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs149277638	chr7:4272893-4272894	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs78491883	chr7:4272901-4272902	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs201307576	chr7:4272906-4272907	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs376242565	chr7:4272922-4272923	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs144472783	chr7:4272924-4272925	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs561998612	chr7:4272925-4272926	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs369276316	chr7:4272926-4272927	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Chordoma	21602918	CNVD
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
Spondylocostal dysostosis	21085971	CNVD
Mental retardation	17901693	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	22286061	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	20164920	CNVD
Colorectal cancer	21645411	CNVD
Intellectual disability	21811512	CNVD
Breast cancer	22522925	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Urothelial carcinoma	21177765	CNVD
Glioblastoma multiforme	21525872	CNVD

Chromatin state (count:439 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:4235800-4287200	Weak transcription	Gastric	stomach
2	chr7:4244400-4283800	Weak transcription	Primary neutrophils fromperipheralblood	blood
3	chr7:4244800-4283800	Weak transcription	Right Ventricle	heart
4	chr7:4251000-4276600	Weak transcription	Aorta	Aorta
5	chr7:4255800-4284200	Weak transcription	Colon Smooth Muscle	Colon
6	chr7:4256000-4283800	Weak transcription	Adipose Nuclei	Adipose
7	chr7:4256400-4283800	Weak transcription	Stomach Smooth Muscle	stomach
8	chr7:4259800-4283600	Weak transcription	Duodenum Smooth Muscle	Duodenum
9	chr7:4261200-4285000	Weak transcription	Rectal Smooth Muscle	rectum
10	chr7:4263800-4273200	Weak transcription	Pancreas	Pancrea
11	chr7:4263800-4281200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr7:4265200-4283600	Weak transcription	Fetal Lung	lung
13	chr7:4266200-4273400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr7:4266200-4279200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr7:4267000-4276000	Weak transcription	Spleen	Spleen
16	chr7:4267800-4275200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr7:4267800-4281200	Weak transcription	Cortex derived primary cultured neurospheres	brain
18	chr7:4267800-4284400	Weak transcription	Fetal Brain Female	brain
19	chr7:4268000-4274400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr7:4268000-4277200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr7:4268000-4291800	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr7:4268200-4284000	Weak transcription	Fetal Muscle Leg	muscle
23	chr7:4268600-4272800	Weak transcription	Fetal Stomach	stomach
24	chr7:4269200-4282600	Weak transcription	Pancreatic Islets	Pancreatic Islet
25	chr7:4270400-4272600	Weak transcription	Fetal Brain Male	brain
26	chr7:4271000-4283400	Weak transcription	Skeletal Muscle Male	skeletal muscle
27	chr7:4272000-4272800	Weak transcription	Fetal Intestine Small	intestine
28	chr7:4272200-4274000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr7:4272800-4273200	Strong transcription	Fetal Intestine Small	intestine
30	chr7:4272800-4282600	Strong transcription	Fetal Stomach	stomach
31	chr7:4273200-4273400	Strong transcription	Pancreas	Pancrea
32	chr7:4273200-4274800	Genic enhancers	Fetal Intestine Small	intestine
33	chr7:4273400-4274000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr7:4273400-4274000	Weak transcription	Pancreas	Pancrea
35	chr7:4273600-4275000	Enhancers	Fetal Intestine Large	intestine
36	chr7:4274000-4274600	Strong transcription	Pancreas	Pancrea
37	chr7:4274000-4277000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr7:4274000-4279200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr7:4274400-4274800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr7:4274400-4275800	Enhancers	HepG2	liver
41	chr7:4274600-4281400	Weak transcription	Pancreas	Pancrea
42	chr7:4274800-4277000	Weak transcription	Fetal Intestine Small	intestine
43	chr7:4274800-4277200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr7:4275000-4275400	Weak transcription	Fetal Intestine Large	intestine
45	chr7:4275200-4275600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr7:4275400-4275600	Enhancers	Fetal Intestine Large	intestine
47	chr7:4275400-4277200	Weak transcription	Lung	lung
48	chr7:4275600-4277000	Weak transcription	Fetal Intestine Large	intestine
49	chr7:4275600-4287800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr7:4275800-4279600	Weak transcription	HepG2	liver

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