Variant report

Variant	nsv1033564
Chromosome Location	chr7:40273845-40417886
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	ATF1	chr7:40386153-40386787	K562	blood:	n/a	n/a
2	ATF1	chr7:40369219-40369450	K562	blood:	n/a	n/a
3	BACH1	chr7:40335510-40335517	K562	blood:	n/a	n/a
4	BCL3	chr7:40396941-40397261	GM12878	blood:	n/a	n/a
5	BHLHE40	chr7:40369274-40369393	GM12878	blood:	n/a	n/a
6	BHLHE40	chr7:40371071-40371334	K562	blood:	n/a	n/a
7	BHLHE40	chr7:40280341-40280356	K562	blood:	n/a	n/a
8	CEBPB	chr7:40413702-40413911	IMR90	lung:	n/a	n/a
9	CEBPB	chr7:40400497-40400736	IMR90	lung:	n/a	chr7:40400597-40400608
10	CEBPB	chr7:40394474-40394666	HepG2	liver:	n/a	chr7:40394598-40394609
11	CEBPB	chr7:40305500-40305758	IMR90	lung:	n/a	chr7:40305633-40305644 chr7:40305631-40305644 chr7:40305631-40305644 chr7:40305631-40305644
12	CEBPB	chr7:40394430-40394767	IMR90	lung:	n/a	chr7:40394598-40394609
13	CEBPB	chr7:40346853-40346935	HepG2	liver:	n/a	chr7:40346890-40346901
14	CEBPB	chr7:40352312-40352434	HepG2	liver:	n/a	chr7:40352333-40352344
15	CEBPB	chr7:40386245-40386478	K562	blood:	n/a	n/a
16	CEBPB	chr7:40400575-40400713	HepG2	liver:	n/a	chr7:40400597-40400608
17	CEBPB	chr7:40400524-40400714	A549	lung:	n/a	chr7:40400597-40400608
18	CHD1	chr7:40369385-40369414	GM12878	blood:	n/a	n/a
19	CHD2	chr7:40386347-40386531	K562	blood:	n/a	n/a
20	CHD2	chr7:40273928-40274040	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr7:40369195-40369470	Medullo	brain:	n/a	chr7:40369339-40369357 chr7:40369340-40369356 chr7:40369341-40369362
22	CTCF	chr7:40369260-40369410	HBMEC	blood vessel:	n/a	chr7:40369339-40369357 chr7:40369340-40369356 chr7:40369341-40369362
23	CTCF	chr7:40369260-40369410	HCPEpiC	choroid plexus:	n/a	chr7:40369339-40369357 chr7:40369340-40369356 chr7:40369341-40369362
24	CTCF	chr7:40371340-40371490	BE2_C	brain:	n/a	n/a
25	CTCF	chr7:40369240-40369390	RPTEC	kidney:	n/a	chr7:40369339-40369357 chr7:40369340-40369356 chr7:40369341-40369362
26	CTCF	chr7:40369060-40369062	GM19240	blood:	n/a	n/a
27	CTCF	chr7:40369144-40369472	ECC-1	luminal epithelium:	n/a	chr7:40369339-40369357 chr7:40369340-40369356 chr7:40369341-40369362
28	CTCF	chr7:40397360-40397510	AG04450	lung:	n/a	n/a
29	CTCF	chr7:40293160-40293310	K562	blood:	n/a	n/a
30	CTCF	chr7:40369280-40369430	HA-sp	spinal cord:	n/a	chr7:40369339-40369357 chr7:40369340-40369356 chr7:40369341-40369362
31	CTCF	chr7:40335860-40336010	HEEpiC	esophagus:	n/a	n/a
32	CTCF	chr7:40369128-40369601	IMR90	lung:	n/a	chr7:40369339-40369357 chr7:40369340-40369356 chr7:40369341-40369362
33	CTCF	chr7:40293160-40293310	AG09309	skin:	n/a	n/a
34	CTCF	chr7:40369240-40369390	BE2_C	brain:	n/a	chr7:40369339-40369357 chr7:40369340-40369356 chr7:40369341-40369362
35	CTCF	chr7:40369300-40369450	GM12868	blood:	n/a	chr7:40369339-40369357 chr7:40369340-40369356 chr7:40369341-40369362
36	CTCF	chr7:40293120-40293270	K562	blood:	n/a	n/a
37	CTCF	chr7:40369260-40369410	HVMF	connective:	n/a	chr7:40369339-40369357 chr7:40369340-40369356 chr7:40369341-40369362
38	CTCF	chr7:40293160-40293310	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr7:40369190-40369458	Gliobla	brain:	n/a	chr7:40369339-40369357 chr7:40369340-40369356 chr7:40369341-40369362
40	CTCF	chr7:40369220-40369370	GM12866	blood:	n/a	chr7:40369339-40369357 chr7:40369340-40369356 chr7:40369341-40369362
41	CTCF	chr7:40369260-40369410	HUVEC	blood vessel:	n/a	chr7:40369339-40369357 chr7:40369340-40369356 chr7:40369341-40369362
42	CTCF	chr7:40369240-40369390	GM12868	blood:	n/a	chr7:40369339-40369357 chr7:40369340-40369356 chr7:40369341-40369362
43	CTCF	chr7:40397400-40397550	HMF	breast:	n/a	n/a
44	CTCF	chr7:40293140-40293290	AG04449	skin:	n/a	n/a
45	CTCF	chr7:40293160-40293310	HBMEC	blood vessel:	n/a	n/a
46	CTCF	chr7:40369229-40369438	LNCaP	prostate:	n/a	chr7:40369339-40369357 chr7:40369340-40369356 chr7:40369341-40369362
47	CTCF	chr7:40369340-40369490	HAc	cerebellar:	n/a	chr7:40369340-40369356 chr7:40369341-40369362
48	CTCF	chr7:40293160-40293310	RPTEC	kidney:	n/a	n/a
49	CTCF	chr7:40293161-40293355	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr7:40293000-40293150	HVMF	connective:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:40338163-40338213	HCF	heart:	n/a
2	chr7:40338163-40338213	HCF	heart:	n/a
3	chr7:40338163-40338213	HEK293	kidney:	embryo
4	chr7:40338163-40338213	BE2_C	brain:	n/a
5	chr7:40367873-40367923	SAEC	small airway:	n/a
6	chr7:40367873-40367923	HRCEpiC	kidney:	n/a
7	chr7:40338163-40338213	Hela-S3	cervix:	n/a
8	chr7:40367873-40367923	HCF	heart:	n/a
9	chr7:40338163-40338213	Hepatocyte	liver:	n/a
10	chr7:40338163-40338213	AG04449	skin:	fetal
11	chr7:40367873-40367923	NB4	blood:	n/a
12	chr7:40367873-40367923	Hepatocyte	liver:	n/a
13	chr7:40367873-40367923	LNCaP	prostate:	n/a
14	chr7:40367873-40367923	HepG2	liver:	n/a
15	chr7:40367873-40367923	K562	blood:	n/a
16	chr7:40338163-40338213	GM19239	blood:	n/a
17	chr7:40367873-40367923	Caco-2	colon:	n/a
18	chr7:40338163-40338213	RPTEC	kidney:	n/a
19	chr7:40338163-40338213	NT2-D1	testis:	n/a
20	chr7:40338163-40338213	SK-N-SH	brain:	n/a
21	chr7:40338163-40338213	MCF10A-Er-Src	breast:	n/a
22	chr7:40367873-40367923	HCT-116	colon:	n/a
23	chr7:40367873-40367923	PANC-1	pancreas:	n/a
24	chr7:40367873-40367923	ECC-1	luminal epithelium:	n/a
25	chr7:40338163-40338213	HAEpiC	amniotic membrane:	n/a
26	chr7:40338163-40338213	NHDF-neo	bronchial:	n/a
27	chr7:40367873-40367923	NHDF-neo	bronchial:	n/a
28	chr7:40367873-40367923	HPAEpiC	pulmonary alveolar:	n/a
29	chr7:40367873-40367923	Jurkat	blood:	n/a
30	chr7:40367873-40367923	GM12892	blood:	n/a
31	chr7:40367873-40367923	GM12878	blood:	n/a
32	chr7:40367873-40367923	ovcar-3	ovarian:	n/a
33	chr7:40338163-40338213	T-47D	breast:	n/a
34	chr7:40338163-40338213	NH-A	brain:	n/a
35	chr7:40367873-40367923	HRE	kidney:	n/a
36	chr7:40338163-40338213	GM12878	blood:	n/a
37	chr7:40367873-40367923	HCM	heart:	n/a
38	chr7:40367873-40367923	SK-N-SH_RA	brain:	n/a
39	chr7:40338163-40338213	ECC-1	luminal epithelium:	n/a
40	chr7:40367873-40367923	HCPEpiC	choroid plexus:	n/a
41	chr7:40367873-40367923	HUVEC	blood vessel:	n/a
42	chr7:40338163-40338213	NB4	blood:	n/a
43	chr7:40367873-40367923	A549	lung:	n/a
44	chr7:40367873-40367923	HAEpiC	amniotic membrane:	n/a
45	chr7:40338163-40338213	SKMC	muscle:	n/a
46	chr7:40367873-40367923	MCF10A-Er-Src	breast:	n/a
47	chr7:40338163-40338213	BJ	skin:	n/a
48	chr7:40338163-40338213	HIPEpiC	eye:	n/a
49	chr7:40338163-40338213	AG09309	skin:	n/a
50	chr7:40338163-40338213	Jurkat	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:6483244..6484243-chr7:40333894..40334600,2	MCF-7	breast:
2	chr7:40344397..40346549-chr7:40349560..40351479,2	K562	blood:
3	chr7:40362786..40364533-chr7:40364996..40369227,3	K562	blood:
4	chr20:57473196..57474009-chr7:40413360..40414065,2	MCF-7	breast:
5	chr7:40345049..40347172-chr7:40349979..40352115,2	K562	blood:
6	chr7:40345049..40347172-chr7:40349979..40352115,2	K562	blood:
7	chr7:40334583..40336119-chr7:40353617..40356349,2	K562	blood:
8	chr7:40344397..40346549-chr7:40349560..40351479,2	K562	blood:
9	chr7:40368904..40369830-chr7:40644119..40645087,4	MCF-7	breast:
10	chr7:40334583..40336119-chr7:40353617..40356349,2	K562	blood:
11	chr7:40362786..40364533-chr7:40364996..40369227,3	K562	blood:
12	chr7:40348620..40350328-chr7:40353767..40356702,2	K562	blood:
13	chr7:40348620..40350328-chr7:40353767..40356702,2	K562	blood:
14	chr7:39988445..39991258-chr7:40413776..40416750,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C7orf11-8	chr7:40279515-40279605	NONHSAT120249
2	lnc-C7orf11-8	chr7:40336722-40336813	NONHSAT120249
3	lnc-C7orf11-8	chr7:40291369-40291524	NONHSAT120249
4	lnc-C7orf11-8	chr7:40333941-40333997	NONHSAT120249

Variant related genes	Relation type
SUGCT	TF binding region
SUGCT	CpG island
ENSG00000065883	chromatin interactions
ENSG00000259826	chromatin interactions

Extended variants
information (count: 4809 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:4809 , 50 per page) page: 1 2 3 4 5 6 7 ... 97

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs113760084	chr7:40273884-40273885	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs538398596	chr7:40273957-40273958	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs554773680	chr7:40273991-40273992	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs574937001	chr7:40273994-40273995	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs146496522	chr7:40273999-40274000	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs556453496	chr7:40274024-40274025	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs62456127	chr7:40274050-40274051	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs538557991	chr7:40274060-40274061	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs558101924	chr7:40274072-40274073	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs368184713	chr7:40274075-40274076	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs577294149	chr7:40274115-40274116	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs192097212	chr7:40274126-40274127	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs562767559	chr7:40274143-40274144	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs34639074	chr7:40274165-40274166	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs182160558	chr7:40274178-40274179	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs548319013	chr7:40274198-40274199	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs556650960	chr7:40274231-40274232	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs561732077	chr7:40274232-40274233	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs148302818	chr7:40274339-40274340	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs547077542	chr7:40274399-40274400	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs570144544	chr7:40274406-40274407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs373313283	chr7:40274448-40274449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs141392684	chr7:40274461-40274462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs569491684	chr7:40274462-40274463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs13243187	chr7:40274509-40274510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs13243188	chr7:40274512-40274513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs13243192	chr7:40274519-40274520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs13243196	chr7:40274526-40274527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs111339178	chr7:40274529-40274530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs112045053	chr7:40274597-40274598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs538056530	chr7:40274634-40274635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs574184035	chr7:40274635-40274636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs186828192	chr7:40274721-40274722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs534321206	chr7:40274736-40274737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs371146668	chr7:40274788-40274789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs190712900	chr7:40274793-40274794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs546138854	chr7:40274837-40274838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs556188704	chr7:40274847-40274848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs576334723	chr7:40274855-40274856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs373058065	chr7:40274909-40274910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs202094229	chr7:40274916-40274917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs73131776	chr7:40274924-40274925	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs67382823	chr7:40274931-40274932	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs556083841	chr7:40274954-40274955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs572085911	chr7:40274959-40274960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs150906000	chr7:40274963-40274964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs563801129	chr7:40274973-40274974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs374042666	chr7:40274987-40274988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs544529370	chr7:40275074-40275075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs113090555	chr7:40275082-40275083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	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
Autism	22495311	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	17237825	CNVD
Breast cancer	17899364	CNVD
Breast cancer	20409316	CNVD
Acute monocytic leukemia	16498392	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Colorectal cancer	19455253	CNVD
Glioblastoma multiforme	22286061	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Gastric cancer	24379144	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:459 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:40272200-40281200	Weak transcription	HSMMtube	muscle
2	chr7:40272200-40285000	Weak transcription	HSMM	muscle
3	chr7:40272200-40303400	Weak transcription	Liver	Liver
4	chr7:40273400-40274000	Enhancers	Primary T killer memory cells from peripheral blood	blood
5	chr7:40273400-40274400	Enhancers	Fetal Intestine Large	intestine
6	chr7:40273400-40274400	Enhancers	Rectal Mucosa Donor 29	rectum
7	chr7:40273600-40274000	Enhancers	Primary hematopoietic stem cells	blood
8	chr7:40273600-40274000	Enhancers	Primary T helper naive cells from peripheral blood	blood
9	chr7:40273600-40274000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
10	chr7:40273600-40274000	Enhancers	Rectal Mucosa Donor 31	rectum
11	chr7:40273600-40274200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
12	chr7:40273600-40274200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr7:40273600-40274200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr7:40273600-40274200	Enhancers	Fetal Thymus	thymus
15	chr7:40273600-40274400	Enhancers	Dnd41	blood
16	chr7:40273800-40274000	Flanking Active TSS	Stomach Mucosa	stomach
17	chr7:40273800-40274200	Enhancers	Primary T cells fromperipheralblood	blood
18	chr7:40273800-40274200	Enhancers	Duodenum Mucosa	Duodenum
19	chr7:40273800-40274200	Enhancers	GM12878-XiMat	blood
20	chr7:40273800-40274400	Enhancers	Fetal Intestine Small	intestine
21	chr7:40274000-40274200	Enhancers	Stomach Mucosa	stomach
22	chr7:40274200-40274400	Flanking Active TSS	Stomach Mucosa	stomach
23	chr7:40274200-40277200	Weak transcription	GM12878-XiMat	blood
24	chr7:40274400-40279800	Weak transcription	Stomach Mucosa	stomach
25	chr7:40274400-40280000	Weak transcription	Fetal Intestine Small	intestine
26	chr7:40277200-40277600	Enhancers	GM12878-XiMat	blood
27	chr7:40279200-40279800	Weak transcription	Duodenum Mucosa	Duodenum
28	chr7:40279200-40280600	Enhancers	Fetal Heart	heart
29	chr7:40279600-40280200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr7:40279800-40280400	Enhancers	Stomach Mucosa	stomach
31	chr7:40279800-40280600	Enhancers	Duodenum Mucosa	Duodenum
32	chr7:40280000-40281000	Enhancers	Fetal Intestine Small	intestine
33	chr7:40280200-40280400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr7:40280200-40280600	Enhancers	Fetal Kidney	kidney
35	chr7:40280200-40280600	Enhancers	Pancreas	Pancrea
36	chr7:40280200-40280600	Enhancers	Right Atrium	heart
37	chr7:40280200-40281000	Enhancers	Fetal Intestine Large	intestine
38	chr7:40280400-40282000	Weak transcription	Stomach Mucosa	stomach
39	chr7:40280400-40284000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr7:40280600-40291800	Weak transcription	Pancreas	Pancrea
41	chr7:40281000-40295000	Weak transcription	Fetal Intestine Small	intestine
42	chr7:40282000-40282600	Enhancers	Stomach Mucosa	stomach
43	chr7:40282600-40283200	Weak transcription	Stomach Mucosa	stomach
44	chr7:40283200-40283400	Enhancers	Stomach Mucosa	stomach
45	chr7:40283800-40284200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr7:40283800-40284200	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr7:40283800-40284200	Enhancers	Ovary	ovary
48	chr7:40284000-40284600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr7:40286400-40287200	Enhancers	Fetal Heart	heart
50	chr7:40286800-40287000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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