Variant report

Variant	nsv892630
Chromosome Location	chr9:15554960-15694690
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	chr9:15606729-15607013	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:15642421-15642732	HepG2	liver:	n/a	n/a
3	ATF1	chr9:15606159-15606277	K562	blood:	n/a	n/a
4	ATF3	chr9:15587162-15587411	K562	blood:	n/a	n/a
5	BATF	chr9:15613003-15613305	GM12878	blood:	n/a	chr9:15613158-15613169
6	BATF	chr9:15612994-15613254	GM12878	blood:	n/a	chr9:15613158-15613169
7	CEBPB	chr9:15634650-15635051	HepG2	liver:	n/a	chr9:15634719-15634730
8	CEBPB	chr9:15616839-15617368	HepG2	liver:	n/a	chr9:15617185-15617196
9	CEBPB	chr9:15634699-15634857	A549	lung:	n/a	chr9:15634719-15634730
10	CEBPB	chr9:15587156-15587411	K562	blood:	n/a	chr9:15587301-15587312
11	CEBPB	chr9:15587130-15587433	IMR90	lung:	n/a	chr9:15587301-15587312
12	CEBPB	chr9:15634610-15635086	IMR90	lung:	n/a	chr9:15634719-15634730
13	CEBPB	chr9:15578740-15579055	IMR90	lung:	n/a	n/a
14	CEBPB	chr9:15587167-15587391	HepG2	liver:	n/a	chr9:15587301-15587312
15	CREB1	chr9:15612874-15613444	GM12878	blood:	n/a	n/a
16	CREB1	chr9:15613014-15613393	GM12878	blood:	n/a	n/a
17	CTCF	chr9:15606780-15606930	AG04450	lung:	n/a	chr9:15606835-15606851 chr9:15606834-15606852 chr9:15606839-15606847 chr9:15606836-15606849 chr9:15606829-15606850
18	CTCF	chr9:15606751-15606936	GM10248	blood:	n/a	chr9:15606835-15606851 chr9:15606834-15606852 chr9:15606839-15606847 chr9:15606836-15606849 chr9:15606829-15606850
19	CTCF	chr9:15606639-15606923	A549	lung:	n/a	chr9:15606835-15606851 chr9:15606834-15606852 chr9:15606839-15606847 chr9:15606836-15606849 chr9:15606829-15606850
20	CTCF	chr9:15620540-15620690	HCPEpiC	choroid plexus:	n/a	n/a
21	CTCF	chr9:15620500-15620650	HBMEC	blood vessel:	n/a	n/a
22	CTCF	chr9:15642420-15642570	AG04449	skin:	n/a	chr9:15642533-15642551 chr9:15642528-15642549 chr9:15642535-15642548
23	CTCF	chr9:15656237-15656340	GM19238	blood:	n/a	n/a
24	CTCF	chr9:15606780-15606930	AG10803	skin:	n/a	chr9:15606835-15606851 chr9:15606834-15606852 chr9:15606839-15606847 chr9:15606836-15606849 chr9:15606829-15606850
25	CTCF	chr9:15622613-15622968	IMR90	lung:	n/a	chr9:15622788-15622796 chr9:15622783-15622801 chr9:15622778-15622799
26	CTCF	chr9:15606820-15606970	GM12868	blood:	n/a	chr9:15606835-15606851 chr9:15606834-15606852 chr9:15606839-15606847 chr9:15606836-15606849 chr9:15606829-15606850
27	CTCF	chr9:15606760-15606910	HBMEC	blood vessel:	n/a	chr9:15606835-15606851 chr9:15606834-15606852 chr9:15606839-15606847 chr9:15606836-15606849 chr9:15606829-15606850
28	CTCF	chr9:15622720-15622870	HBMEC	blood vessel:	n/a	chr9:15622788-15622796 chr9:15622783-15622801 chr9:15622778-15622799
29	CTCF	chr9:15642480-15642630	HCPEpiC	choroid plexus:	n/a	chr9:15642533-15642551 chr9:15642528-15642549 chr9:15642535-15642548
30	CTCF	chr9:15656260-15656410	HepG2	liver:	n/a	n/a
31	CTCF	chr9:15620560-15620710	RPTEC	kidney:	n/a	n/a
32	CTCF	chr9:15606786-15606925	MCF-7	breast:	n/a	chr9:15606835-15606851 chr9:15606834-15606852 chr9:15606839-15606847 chr9:15606836-15606849 chr9:15606829-15606850
33	CTCF	chr9:15606518-15607060	HCT-116	colon:	n/a	chr9:15606835-15606851 chr9:15606834-15606852 chr9:15606839-15606847 chr9:15606836-15606849 chr9:15606829-15606850
34	CTCF	chr9:15620500-15620650	HMF	breast:	n/a	n/a
35	CTCF	chr9:15656196-15656346	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr9:15642440-15642590	GM12867	blood:	n/a	chr9:15642533-15642551 chr9:15642528-15642549 chr9:15642535-15642548
37	CTCF	chr9:15622577-15622945	HCT-116	colon:	n/a	chr9:15622788-15622796 chr9:15622783-15622801 chr9:15622778-15622799
38	CTCF	chr9:15622740-15622869	GM10266	blood:	n/a	chr9:15622788-15622796 chr9:15622783-15622801 chr9:15622778-15622799
39	CTCF	chr9:15642380-15642530	HCT-116	colon:	n/a	n/a
40	CTCF	chr9:15642440-15642590	HEEpiC	esophagus:	n/a	chr9:15642533-15642551 chr9:15642528-15642549 chr9:15642535-15642548
41	CTCF	chr9:15620360-15620510	WI-38	lung:	n/a	n/a
42	CTCF	chr9:15622720-15622870	RPTEC	kidney:	n/a	chr9:15622788-15622796 chr9:15622783-15622801 chr9:15622778-15622799
43	CTCF	chr9:15620560-15620710	HEK293	kidney:	n/a	n/a
44	CTCF	chr9:15656154-15656377	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr9:15642415-15642643	Hela-S3	cervix:	n/a	chr9:15642533-15642551 chr9:15642528-15642549 chr9:15642535-15642548
46	CTCF	chr9:15620480-15620630	AG04450	lung:	n/a	n/a
47	CTCF	chr9:15606738-15606990	Pancreas_OC	pancreas:	n/a	chr9:15606835-15606851 chr9:15606834-15606852 chr9:15606839-15606847 chr9:15606836-15606849 chr9:15606829-15606850
48	CTCF	chr9:15642480-15642630	GM12868	blood:	n/a	chr9:15642533-15642551 chr9:15642528-15642549 chr9:15642535-15642548
49	CTCF	chr9:15622735-15622865	GM13977	blood:	n/a	chr9:15622788-15622796 chr9:15622783-15622801 chr9:15622778-15622799
50	CTCF	chr9:15620460-15620610	HFF-Myc	foreskin:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:15609722..15611520-chr9:15613088..15614614,2	MCF-7	breast:
2	chr9:15570769..15573187-chr9:15586351..15588425,2	MCF-7	breast:
3	chr9:15509318..15512022-chr9:15550389..15555494,9	MCF-7	breast:
4	chr9:15690406..15691946-chr9:15692582..15695063,2	MCF-7	breast:
5	chr9:15421567..15424446-chr9:15606338..15608598,2	MCF-7	breast:
6	chr9:15551543..15553297-chr9:15600119..15601625,2	MCF-7	breast:
7	chr9:15551936..15552629-chr9:15619996..15620642,2	MCF-7	breast:
8	chr9:15609722..15611520-chr9:15613088..15614614,2	MCF-7	breast:
9	chr9:15509144..15511285-chr9:15608383..15610950,2	MCF-7	breast:
10	chr9:15690406..15691946-chr9:15692582..15695063,2	MCF-7	breast:
11	chr9:15551939..15552527-chr9:15606365..15606962,2	MCF-7	breast:
12	chr9:15508603..15511423-chr9:15563063..15564927,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SNAPC3-3	chr9:15563976-15564022	NONHSAT130275
2	lnc-SNAPC3-4	chr9:15588353-15588613	NONHSAT130276

Variant related genes	Relation type
HMGN2P16	TF binding region
ENSG00000164975	chromatin interactions
ENSG00000164985	chromatin interactions
ENSG00000231376	chromatin interactions
ENSG00000164989	chromatin interactions

Extended variants
information (count: 7415 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:7415 , 50 per page) page: 1 2 3 4 5 6 7 ... 149

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4740614	chr9:15554960-15554961	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs186106371	chr9:15554970-15554971	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs75925639	chr9:15554979-15554980	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs188909595	chr9:15555000-15555001	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs138917755	chr9:15555031-15555032	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs10962066	chr9:15555038-15555039	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs149391857	chr9:15555104-15555105	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs559421832	chr9:15555105-15555106	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs144845854	chr9:15555122-15555123	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs548507264	chr9:15555174-15555175	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs569749481	chr9:15555208-15555209	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs117085729	chr9:15555222-15555223	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs552346921	chr9:15555263-15555264	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs570625393	chr9:15555281-15555282	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs571389542	chr9:15555314-15555315	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs534668878	chr9:15555322-15555323	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs552927014	chr9:15555348-15555349	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs568150453	chr9:15555370-15555371	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs535763872	chr9:15555381-15555382	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs375226145	chr9:15555387-15555388	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs181324878	chr9:15555454-15555455	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs7873152	chr9:15555458-15555459	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs540039779	chr9:15555463-15555464	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs186388411	chr9:15555518-15555519	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs373079254	chr9:15555582-15555583	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs148578067	chr9:15555597-15555598	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs375879825	chr9:15555602-15555603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs543965336	chr9:15555639-15555640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs58596549	chr9:15555651-15555652	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs545134743	chr9:15555694-15555695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs144481017	chr9:15555724-15555725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs563606534	chr9:15555727-15555728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs191085718	chr9:15555744-15555745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs550605026	chr9:15555759-15555760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs557296461	chr9:15555760-15555761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs563967720	chr9:15555789-15555790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs60918672	chr9:15555805-15555806	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs117746357	chr9:15555811-15555812	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
39	rs535868443	chr9:15555853-15555854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs182977193	chr9:15555855-15555856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs185075989	chr9:15555859-15555860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs550959215	chr9:15555873-15555874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs112280707	chr9:15555880-15555881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs200282635	chr9:15555888-15555889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs143745148	chr9:15555893-15555894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs370144676	chr9:15555894-15555895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs151261997	chr9:15555899-15555900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs140305310	chr9:15555909-15555910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs534706764	chr9:15555933-15555934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs553108068	chr9:15555952-15555953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Melanoma	18172304	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Myelodysplastic syndrome	21251322	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	18803288	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21611746	CNVD
Glycine encephalopathy	21572526	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	19835627	CNVD
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:331 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:15553200-15555000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr9:15553800-15576200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr9:15553800-15580600	Weak transcription	Ovary	ovary
4	chr9:15553800-15592600	Weak transcription	Left Ventricle	heart
5	chr9:15554000-15564400	Weak transcription	Skeletal Muscle Male	skeletal muscle
6	chr9:15554000-15590200	Weak transcription	Fetal Stomach	stomach
7	chr9:15554400-15579400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr9:15554600-15555000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr9:15554600-15555600	Enhancers	Thymus	Thymus
10	chr9:15554600-15556400	Weak transcription	Fetal Brain Male	brain
11	chr9:15554600-15563600	Weak transcription	Fetal Thymus	thymus
12	chr9:15554600-15580800	Weak transcription	Brain Anterior Caudate	brain
13	chr9:15554800-15555000	Enhancers	GM12878-XiMat	blood
14	chr9:15554800-15559400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr9:15554800-15559600	Weak transcription	Primary hematopoietic stem cells	blood
16	chr9:15554800-15560800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
17	chr9:15555000-15555200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr9:15555200-15559400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr9:15555600-15561600	Weak transcription	Thymus	Thymus
20	chr9:15559400-15559600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr9:15559400-15559800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr9:15559600-15560400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr9:15559600-15561800	Strong transcription	Primary hematopoietic stem cells	blood
24	chr9:15559800-15560600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr9:15560400-15563000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr9:15560600-15562400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr9:15560800-15562200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
28	chr9:15561600-15561800	Enhancers	Sigmoid Colon	Sigmoid Colon
29	chr9:15561600-15562400	Strong transcription	Thymus	Thymus
30	chr9:15561800-15563400	Weak transcription	Sigmoid Colon	Sigmoid Colon
31	chr9:15561800-15570000	Weak transcription	Primary hematopoietic stem cells	blood
32	chr9:15562200-15588200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
33	chr9:15562400-15570400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr9:15562400-15583800	Weak transcription	Thymus	Thymus
35	chr9:15563000-15563800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr9:15563600-15565000	Strong transcription	Fetal Thymus	thymus
37	chr9:15563800-15569400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr9:15564000-15564800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr9:15565000-15578800	Weak transcription	Fetal Thymus	thymus
40	chr9:15569400-15572400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr9:15570000-15570600	Strong transcription	Primary hematopoietic stem cells	blood
42	chr9:15570400-15571000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr9:15570600-15574800	Weak transcription	Primary hematopoietic stem cells	blood
44	chr9:15571000-15574600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr9:15572200-15573200	Enhancers	Fetal Lung	lung
46	chr9:15572400-15580800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr9:15573200-15576600	Weak transcription	Fetal Lung	lung
48	chr9:15574600-15580000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr9:15574800-15579400	Strong transcription	Primary hematopoietic stem cells	blood
50	chr9:15576200-15576800	Strong transcription	Breast Myoepithelial Primary Cells	Breast

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