Variant report

Variant	nsv824000
Chromosome Location	chr7:6492407-6499407
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	chr7:6493526-6493770	K562	blood:	n/a	n/a
2	BCL3	chr7:6493126-6493626	A549	lung:	n/a	n/a
3	CEBPB	chr7:6492557-6492846	MCF-7	breast:	n/a	chr7:6492671-6492682
4	CEBPB	chr7:6493268-6493680	A549	lung:	n/a	n/a
5	CEBPB	chr7:6493180-6493789	A549	lung:	n/a	n/a
6	CEBPB	chr7:6492513-6492835	Hela-S3	cervix:	n/a	chr7:6492671-6492682
7	CEBPB	chr7:6493281-6493607	A549	lung:	n/a	n/a
8	CEBPB	chr7:6492582-6492876	A549	lung:	n/a	chr7:6492671-6492682
9	CEBPB	chr7:6492573-6492791	IMR90	lung:	n/a	chr7:6492671-6492682
10	CEBPB	chr7:6492587-6492860	MCF-7	breast:	n/a	chr7:6492671-6492682
11	CEBPB	chr7:6493283-6493673	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr7:6492537-6492830	A549	lung:	n/a	chr7:6492671-6492682
13	CEBPB	chr7:6492480-6492944	A549	lung:	n/a	chr7:6492671-6492682
14	CEBPB	chr7:6493374-6493550	HepG2	liver:	n/a	n/a
15	CEBPB	chr7:6493257-6493779	IMR90	lung:	n/a	n/a
16	CEBPB	chr7:6492559-6492830	HepG2	liver:	n/a	chr7:6492671-6492682
17	CTCF	chr7:6493471-6493530	MCF-7	breast:	n/a	n/a
18	CTCF	chr7:6495817-6495828	GM10248	blood:	n/a	n/a
19	CTCF	chr7:6493412-6493563	NHEK	skin:	n/a	n/a
20	CTCF	chr7:6493420-6493570	HMEC	breast:	n/a	n/a
21	CTCF	chr7:6493432-6493556	Hela-S3	cervix:	n/a	n/a
22	EGR1	chr7:6499099-6499365	K562	blood:	n/a	chr7:6499291-6499302 chr7:6499290-6499303 chr7:6499289-6499303 chr7:6499291-6499302 chr7:6499291-6499300 chr7:6499285-6499307 chr7:6499289-6499304 chr7:6499291-6499301 chr7:6499292-6499301 chr7:6499290-6499303 chr7:6499291-6499301
23	EGR1	chr7:6499134-6499344	K562	blood:	n/a	chr7:6499291-6499302 chr7:6499290-6499303 chr7:6499289-6499303 chr7:6499291-6499302 chr7:6499291-6499300 chr7:6499285-6499307 chr7:6499289-6499304 chr7:6499291-6499301 chr7:6499292-6499301 chr7:6499290-6499303 chr7:6499291-6499301
24	EP300	chr7:6493262-6493861	A549	lung:	n/a	n/a
25	FOS	chr7:6493337-6493787	MCF10A-Er-Src	breast:	n/a	n/a
26	FOS	chr7:6493299-6493790	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr7:6498340-6498635	MCF10A-Er-Src	breast:	n/a	chr7:6498491-6498501 chr7:6498491-6498501
28	FOS	chr7:6493245-6493828	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr7:6498473-6498568	MCF10A-Er-Src	breast:	n/a	chr7:6498491-6498501 chr7:6498491-6498501
30	FOS	chr7:6493365-6493781	MCF10A-Er-Src	breast:	n/a	n/a
31	FOSL1	chr7:6493226-6493894	HCT-116	colon:	n/a	n/a
32	FOSL1	chr7:6493273-6493919	HCT-116	colon:	n/a	n/a
33	FOSL2	chr7:6493280-6493860	A549	lung:	n/a	n/a
34	FOSL2	chr7:6493137-6493906	SK-N-SH	brain:	n/a	n/a
35	FOSL2	chr7:6493354-6493765	A549	lung:	n/a	n/a
36	FOSL2	chr7:6499094-6501279	HepG2	liver:	n/a	n/a
37	GATA3	chr7:6493105-6493891	A549	lung:	n/a	n/a
38	JUND	chr7:6493116-6494003	SK-N-SH	brain:	n/a	chr7:6493543-6493554
39	JUND	chr7:6493225-6493921	HCT-116	colon:	n/a	chr7:6493543-6493554
40	JUND	chr7:6493421-6493678	HepG2	liver:	n/a	chr7:6493543-6493554
41	MAFK	chr7:6495970-6496106	HepG2	liver:	n/a	n/a
42	MYC	chr7:6492535-6492757	MCF10A-Er-Src	breast:	n/a	n/a
43	MYC	chr7:6493307-6493741	MCF10A-Er-Src	breast:	n/a	n/a
44	MYC	chr7:6493331-6493839	MCF10A-Er-Src	breast:	n/a	n/a
45	POLR2A	chr7:6496469-6496770	MCF-7	breast:	n/a	n/a
46	POLR2A	chr7:6499179-6499294	GM12878	blood:	n/a	n/a
47	POLR2A	chr7:6493479-6493625	MCF10A-Er-Src	breast:	n/a	n/a
48	POLR2A	chr7:6499031-6499369	Hela-S3	cervix:	n/a	n/a
49	POLR2A	chr7:6496461-6496485	ProgFib	skin:	n/a	n/a
50	POLR2A	chr7:6498794-6501380	PFSK-1	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:6493555-6493605	Caco-2	colon:	n/a
2	chr7:6493555-6493605	Caco-2	colon:	n/a
3	chr7:6493555-6493605	HRE	kidney:	n/a
4	chr7:6493555-6493605	MCF10A-Er-Src	breast:	n/a
5	chr7:6493555-6493605	GM12878	blood:	n/a
6	chr7:6493555-6493605	AG10803	skin:	n/a
7	chr7:6493555-6493605	PFSK-1	brain:	n/a
8	chr7:6493555-6493605	AoSMC	blood vessel:	n/a
9	chr7:6493555-6493605	GM06990	blood:	n/a
10	chr7:6493555-6493605	HepG2	liver:	n/a
11	chr7:6493555-6493605	SK-N-SH	brain:	n/a
12	chr7:6493555-6493605	H1-hESC	embryonic stem cell:	embryo
13	chr7:6493555-6493605	A549	lung:	n/a
14	chr7:6493555-6493605	HUVEC	blood vessel:	n/a
15	chr7:6493555-6493605	BJ	skin:	n/a
16	chr7:6493555-6493605	SK-N-SH_RA	brain:	n/a
17	chr7:6493555-6493605	HMEC	breast:	n/a
18	chr7:6493555-6493605	NHDF-neo	bronchial:	n/a
19	chr7:6493555-6493605	AG09319	gingival:	n/a
20	chr7:6493555-6493605	NH-A	brain:	n/a
21	chr7:6493555-6493605	K562	blood:	n/a
22	chr7:6493555-6493605	HAEpiC	amniotic membrane:	n/a
23	chr7:6493555-6493605	AG04450	lung:	fetal
24	chr7:6493555-6493605	ECC-1	luminal epithelium:	n/a
25	chr7:6493555-6493605	RPTEC	kidney:	n/a
26	chr7:6493555-6493605	HNPCEpiC	eye:	n/a
27	chr7:6493555-6493605	HCM	heart:	n/a
28	chr7:6493555-6493605	NHBE	bronchial:	n/a
29	chr7:6493555-6493605	NT2-D1	testis:	n/a
30	chr7:6493555-6493605	HEK293	kidney:	embryo
31	chr7:6493555-6493605	HCF	heart:	n/a
32	chr7:6493555-6493605	GM12891	blood:	n/a
33	chr7:6493555-6493605	HEEpiC	esophagus:	n/a
34	chr7:6493555-6493605	IMR90	lung:	fetal
35	chr7:6493555-6493605	HCPEpiC	choroid plexus:	n/a
36	chr7:6493555-6493605	U87	brain:	n/a
37	chr7:6493555-6493605	PrEC	prostate:	n/a
38	chr7:6493555-6493605	HL-60	blood:	n/a
39	chr7:6493555-6493605	GM12892	blood:	n/a
40	chr7:6493555-6493605	PANC-1	pancreas:	n/a
41	chr7:6493555-6493605	HRPEpiC	eye:	n/a
42	chr7:6493555-6493605	MCF-7	breast:	n/a
43	chr7:6493555-6493605	Hepatocyte	liver:	n/a
44	chr7:6493555-6493605	ProgFib	skin:	n/a
45	chr7:6493555-6493605	HPAEpiC	pulmonary alveolar:	n/a
46	chr7:6493555-6493605	AG09309	skin:	n/a
47	chr7:6493555-6493605	GM19239	blood:	n/a
48	chr7:6493555-6493605	T-47D	breast:	n/a
49	chr7:6493555-6493605	LNCaP	prostate:	n/a
50	chr7:6493555-6493605	SKMC	muscle:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:6484395..6490398-chr7:6492212..6496662,5	MCF-7	breast:
2	chr7:6487071..6489296-chr7:6498689..6501637,2	MCF-7	breast:
3	chr7:6486167..6489212-chr7:6498721..6504081,5	MCF-7	breast:
4	chr7:6487534..6489634-chr7:6491176..6495271,6	MCF-7	breast:
5	chr7:6495113..6497493-chr7:6497529..6500079,3	MCF-7	breast:
6	chr7:6497678..6499764-chr7:6515399..6517836,2	K562	blood:
7	chr7:6495113..6497493-chr7:6497529..6500079,3	MCF-7	breast:
8	chr7:6492564..6494087-chr7:6514495..6516683,2	K562	blood:

Variant related genes	Relation type
DAGLB	TF binding region
DAGLB	CpG island
ENSG00000164535	chromatin interactions

Extended variants
information (count: 347 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:347 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530770319	chr7:6492407-6492408	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs537080175	chr7:6492430-6492431	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs59612436	chr7:6492475-6492476	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs567237195	chr7:6492480-6492481	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs534733180	chr7:6492490-6492491	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs553060762	chr7:6492507-6492508	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs578225099	chr7:6492519-6492520	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs57900187	chr7:6492521-6492522	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs187236653	chr7:6492527-6492528	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs552277810	chr7:6492532-6492533	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs11309414	chr7:6492548-6492549	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs540177931	chr7:6492549-6492550	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs543268571	chr7:6492575-6492576	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs561144976	chr7:6492626-6492627	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs117818660	chr7:6492648-6492649	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs7809287	chr7:6492779-6492780	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs7810553	chr7:6492879-6492880	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs111824689	chr7:6492887-6492888	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs533005079	chr7:6492914-6492915	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs551265840	chr7:6492918-6492919	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs563635150	chr7:6492980-6492981	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs137944341	chr7:6492996-6492997	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs13224490	chr7:6493001-6493002	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs376663440	chr7:6493010-6493011	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs549231663	chr7:6493036-6493037	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs567276022	chr7:6493046-6493047	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs190484016	chr7:6493050-6493051	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs183053795	chr7:6493104-6493105	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs187679308	chr7:6493105-6493106	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs539252864	chr7:6493123-6493124	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs149057861	chr7:6493137-6493138	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs11361392	chr7:6493181-6493182	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs565155361	chr7:6493197-6493198	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs34679461	chr7:6493199-6493200	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs575763084	chr7:6493255-6493256	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs143053620	chr7:6493291-6493292	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs200085199	chr7:6493296-6493297	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs559525314	chr7:6493390-6493391	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs572942652	chr7:6493414-6493415	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs540229039	chr7:6493430-6493431	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs565065312	chr7:6493525-6493526	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs533447445	chr7:6493555-6493556	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs544658719	chr7:6493621-6493622	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs551633514	chr7:6493721-6493722	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs563360903	chr7:6493754-6493755	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs530686795	chr7:6493760-6493761	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs569824561	chr7:6493763-6493764	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs148221927	chr7:6493778-6493779	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs118184487	chr7:6493780-6493781	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs528141941	chr7:6493813-6493814	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:75)

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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	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
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
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	21525872	CNVD
Autism	20685689	CNVD
Intracranial arachnoid cysts	20187927	CNVD

Chromatin state (count:170 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:6488200-6492800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr7:6488200-6493200	Weak transcription	HMEC	breast
3	chr7:6488200-6493200	Weak transcription	HSMM	muscle
4	chr7:6488200-6493200	Weak transcription	NH-A	brain
5	chr7:6488200-6493200	Weak transcription	NHLF	lung
6	chr7:6488200-6499600	Weak transcription	Lung	lung
7	chr7:6488200-6499800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr7:6488200-6499800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr7:6488200-6500200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr7:6488200-6500800	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr7:6488400-6500200	Weak transcription	HSMMtube	muscle
12	chr7:6488400-6505200	Weak transcription	Fetal Brain Male	brain
13	chr7:6488400-6505600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr7:6488400-6505600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr7:6488600-6499800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr7:6488600-6500000	Weak transcription	Primary T cells from cord blood	blood
17	chr7:6488800-6492800	Weak transcription	Osteobl	bone
18	chr7:6488800-6493000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr7:6488800-6493200	Weak transcription	NHDF-Ad	bronchial
20	chr7:6488800-6499800	Weak transcription	Fetal Brain Female	brain
21	chr7:6488800-6499800	Weak transcription	Fetal Muscle Leg	muscle
22	chr7:6488800-6500000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr7:6488800-6500000	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr7:6488800-6500000	Weak transcription	Adipose Nuclei	Adipose
25	chr7:6488800-6500000	Weak transcription	Liver	Liver
26	chr7:6488800-6500000	Weak transcription	Rectal Mucosa Donor 29	rectum
27	chr7:6488800-6500200	Weak transcription	Brain Germinal Matrix	brain
28	chr7:6488800-6500200	Weak transcription	Spleen	Spleen
29	chr7:6488800-6500800	Weak transcription	Primary B cells from cord blood	blood
30	chr7:6488800-6500800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
31	chr7:6488800-6501000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
32	chr7:6488800-6505200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
33	chr7:6488800-6505200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
34	chr7:6488800-6505600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
35	chr7:6489000-6493200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr7:6489000-6493200	Weak transcription	NHEK	skin
37	chr7:6489000-6499800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr7:6489000-6499800	Weak transcription	Fetal Muscle Trunk	muscle
39	chr7:6489000-6500000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
40	chr7:6489000-6500000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
41	chr7:6489000-6500000	Weak transcription	Brain Cingulate Gyrus	brain
42	chr7:6489000-6500000	Weak transcription	Monocytes-CD14+_RO01746	blood
43	chr7:6489000-6500200	Weak transcription	Primary monocytes fromperipheralblood	blood
44	chr7:6489000-6500200	Weak transcription	Primary hematopoietic stem cells	blood
45	chr7:6489000-6500200	Weak transcription	Primary T helper cells PMA-I stimulated	--
46	chr7:6489000-6500200	Weak transcription	Primary T helper cells fromperipheralblood	blood
47	chr7:6489000-6500200	Weak transcription	Cortex derived primary cultured neurospheres	brain
48	chr7:6489000-6500200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr7:6489000-6500200	Weak transcription	GM12878-XiMat	blood
50	chr7:6489000-6500400	Weak transcription	Primary neutrophils fromperipheralblood	blood

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