Variant report

Variant	esv3404940
Chromosome Location	chr9:6828615-6836185
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:152)
CpG islands
(count:61)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:152 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr9:6833910-6834257	IMR90	lung:	n/a	n/a
2	CEBPB	chr9:6833914-6834218	A549	lung:	n/a	n/a
3	CEBPB	chr9:6833935-6834181	K562	blood:	n/a	n/a
4	CTCF	chr9:6829180-6829330	HCT-116	colon:	n/a	n/a
5	CTCF	chr9:6828960-6829110	NB4	blood:	n/a	n/a
6	CTCF	chr9:6829140-6829290	HVMF	connective:	n/a	n/a
7	CTCF	chr9:6829120-6829270	HPF	lung:	n/a	n/a
8	CTCF	chr9:6829100-6829250	HBMEC	blood vessel:	n/a	n/a
9	CTCF	chr9:6829600-6829750	GM12864	blood:	n/a	chr9:6829734-6829747
10	CTCF	chr9:6829164-6829218	MCF-7	breast:	n/a	n/a
11	CTCF	chr9:6829060-6829210	AG04449	skin:	n/a	n/a
12	CTCF	chr9:6829080-6829230	GM12873	blood:	n/a	n/a
13	CTCF	chr9:6829060-6829210	HCFaa	heart:	n/a	n/a
14	CTCF	chr9:6829020-6829170	AoAF	blood vessel:	n/a	n/a
15	CTCF	chr9:6829040-6829190	AG10803	skin:	n/a	n/a
16	CTCF	chr9:6829100-6829250	SAEC	small airway:	n/a	n/a
17	CTCF	chr9:6829040-6829190	HEK293	kidney:	n/a	n/a
18	CTCF	chr9:6829080-6829230	AG04449	skin:	n/a	n/a
19	CTCF	chr9:6829120-6829270	AG04450	lung:	n/a	n/a
20	CTCF	chr9:6829155-6829156	NHEK	skin:	n/a	n/a
21	CTCF	chr9:6829000-6829150	HFF-Myc	foreskin:	n/a	n/a
22	CTCF	chr9:6829060-6829210	HEEpiC	esophagus:	n/a	n/a
23	CTCF	chr9:6829080-6829230	MCF-7	breast:	n/a	n/a
24	CTCF	chr9:6829060-6829210	SAEC	small airway:	n/a	n/a
25	CTCF	chr9:6829020-6829170	GM12870	blood:	n/a	n/a
26	CTCF	chr9:6829080-6829230	BE2_C	brain:	n/a	n/a
27	CTCF	chr9:6829100-6829250	AoAF	blood vessel:	n/a	n/a
28	CTCF	chr9:6829080-6829230	GM12871	blood:	n/a	n/a
29	CTCF	chr9:6829060-6829210	GM12864	blood:	n/a	n/a
30	CTCF	chr9:6829600-6829750	MCF-7	breast:	n/a	chr9:6829734-6829747
31	CTCF	chr9:6829180-6829330	RPTEC	kidney:	n/a	n/a
32	CTCF	chr9:6829157-6829225	NHEK	skin:	n/a	n/a
33	CTCF	chr9:6829040-6829190	GM12872	blood:	n/a	n/a
34	CTCF	chr9:6829160-6829310	Caco-2	colon:	n/a	n/a
35	CTCF	chr9:6829169-6829227	Fibrobl	skin:	n/a	n/a
36	CTCF	chr9:6829140-6829290	HepG2	liver:	n/a	n/a
37	CTCF	chr9:6829034-6829312	IMR90	lung:	n/a	n/a
38	CTCF	chr9:6829120-6829270	NHEK	skin:	n/a	n/a
39	CTCF	chr9:6829080-6829230	HMF	breast:	n/a	n/a
40	CTCF	chr9:6829160-6829310	HVMF	connective:	n/a	n/a
41	CTCF	chr9:6829100-6829250	HMF	breast:	n/a	n/a
42	CTCF	chr9:6829060-6829210	HPAF	blood vessel:	n/a	n/a
43	CTCF	chr9:6829000-6829150	HCPEpiC	choroid plexus:	n/a	n/a
44	CTCF	chr9:6829120-6829270	HPAF	blood vessel:	n/a	n/a
45	CTCF	chr9:6829040-6829190	BE2_C	brain:	n/a	n/a
46	CTCF	chr9:6829140-6829290	GM12873	blood:	n/a	n/a
47	CTCF	chr9:6829100-6829250	GM12875	blood:	n/a	n/a
48	CTCF	chr9:6829180-6829330	HFF	foreskin:	n/a	n/a
49	CTCF	chr9:6829040-6829190	RPTEC	kidney:	n/a	n/a
50	CTCF	chr9:6829120-6829270	HA-sp	spinal cord:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:6835001-6835051	HCPEpiC	choroid plexus:	n/a
2	chr9:6835001-6835051	Hepatocyte	liver:	n/a
3	chr9:6835001-6835051	ProgFib	skin:	n/a
4	chr9:6835001-6835051	NHDF-neo	bronchial:	n/a
5	chr9:6835001-6835051	HIPEpiC	eye:	n/a
6	chr9:6835001-6835051	HMEC	breast:	n/a
7	chr9:6835001-6835051	AG09309	skin:	n/a
8	chr9:6835001-6835051	HRPEpiC	eye:	n/a
9	chr9:6835001-6835051	HEEpiC	esophagus:	n/a
10	chr9:6835001-6835051	AG04450	lung:	fetal
11	chr9:6835001-6835051	GM06990	blood:	n/a
12	chr9:6835001-6835051	CMK	blood:	n/a
13	chr9:6835001-6835051	NT2-D1	testis:	n/a
14	chr9:6835001-6835051	HepG2	liver:	n/a
15	chr9:6835001-6835051	HCT-116	colon:	n/a
16	chr9:6835001-6835051	GM12891	blood:	n/a
17	chr9:6835001-6835051	NH-A	brain:	n/a
18	chr9:6835001-6835051	SAEC	small airway:	n/a
19	chr9:6835001-6835051	RPTEC	kidney:	n/a
20	chr9:6835001-6835051	U87	brain:	n/a
21	chr9:6835001-6835051	K562	blood:	n/a
22	chr9:6835001-6835051	GM12892	blood:	n/a
23	chr9:6835001-6835051	PrEC	prostate:	n/a
24	chr9:6835001-6835051	HL-60	blood:	n/a
25	chr9:6835001-6835051	GM19239	blood:	n/a
26	chr9:6835001-6835051	Jurkat	blood:	n/a
27	chr9:6835001-6835051	Caco-2	colon:	n/a
28	chr9:6835001-6835051	ovcar-3	ovarian:	n/a
29	chr9:6835001-6835051	A549	lung:	n/a
30	chr9:6835001-6835051	BJ	skin:	n/a
31	chr9:6835001-6835051	SK-N-SH_RA	brain:	n/a
32	chr9:6835001-6835051	Hela-S3	cervix:	n/a
33	chr9:6835001-6835051	AG04449	skin:	fetal
34	chr9:6835001-6835051	HEK293	kidney:	embryo
35	chr9:6835001-6835051	PFSK-1	brain:	n/a
36	chr9:6835001-6835051	T-47D	breast:	n/a
37	chr9:6835001-6835051	PANC-1	pancreas:	n/a
38	chr9:6835001-6835051	HCF	heart:	n/a
39	chr9:6835001-6835051	HPAEpiC	pulmonary alveolar:	n/a
40	chr9:6835001-6835051	MCF10A-Er-Src	breast:	n/a
41	chr9:6835001-6835051	BE2_C	brain:	n/a
42	chr9:6835001-6835051	IMR90	lung:	fetal
43	chr9:6835001-6835051	NHBE	bronchial:	n/a
44	chr9:6835001-6835051	ECC-1	luminal epithelium:	n/a
45	chr9:6835001-6835051	SK-N-SH	brain:	n/a
46	chr9:6835001-6835051	LNCaP	prostate:	n/a
47	chr9:6835001-6835051	AG09319	gingival:	n/a
48	chr9:6835001-6835051	HUVEC	blood vessel:	n/a
49	chr9:6835001-6835051	GM12878	blood:	n/a
50	chr9:6835001-6835051	NB4	blood:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:6826110..6829506-chr9:6834474..6836178,3	MCF-7	breast:
2	chr9:6826110..6829506-chr9:6834474..6836178,3	MCF-7	breast:
3	chr9:6831771..6833427-chr9:6836426..6839172,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000230581	TF binding region
ENSG00000230581	CpG island

Extended variants
information (count: 426 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:426 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs386732159	chr9:6828630-6828631	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs575618508	chr9:6828653-6828654	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs187667894	chr9:6828676-6828677	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs536404205	chr9:6828698-6828699	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs146395613	chr9:6828711-6828712	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs191741225	chr9:6828732-6828733	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs540303993	chr9:6828817-6828818	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs558393736	chr9:6828827-6828828	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs374534518	chr9:6828828-6828829	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs182533399	chr9:6828858-6828859	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs368678867	chr9:6828859-6828860	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs530325690	chr9:6828867-6828868	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs202106825	chr9:6828875-6828876	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs374608358	chr9:6828884-6828885	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs372006651	chr9:6828915-6828916	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs542157390	chr9:6828966-6828967	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs560722567	chr9:6828971-6828972	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs527907554	chr9:6829010-6829011	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs187188916	chr9:6829015-6829016	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs570872126	chr9:6829102-6829103	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs192215137	chr9:6829120-6829121	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs550201613	chr9:6829153-6829154	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs568511617	chr9:6829193-6829194	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs536539327	chr9:6829200-6829201	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs184538445	chr9:6829208-6829209	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs190297563	chr9:6829213-6829214	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs116257991	chr9:6829258-6829259	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs193299105	chr9:6829260-6829261	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs115351153	chr9:6829262-6829263	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs139043441	chr9:6829355-6829356	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs555731841	chr9:6829405-6829406	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs561800837	chr9:6829432-6829433	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs143999043	chr9:6829435-6829436	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs571024665	chr9:6829464-6829465	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs7870453	chr9:6829508-6829509	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs546089453	chr9:6829520-6829521	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs564556326	chr9:6829540-6829541	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs550181528	chr9:6829541-6829542	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs531837191	chr9:6829545-6829546	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs550336276	chr9:6829551-6829552	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs57498143	chr9:6829553-6829554	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs529331476	chr9:6829588-6829589	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs184296906	chr9:6829626-6829627	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs114963633	chr9:6829627-6829628	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs139534434	chr9:6829660-6829661	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs576447663	chr9:6829669-6829670	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs149713503	chr9:6829695-6829696	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs530612079	chr9:6829725-6829726	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs537533541	chr9:6829740-6829741	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs555868800	chr9:6829741-6829742	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:104)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Intracranial aneurysm	16715129	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Disorders of sex development	22290220	CNVD
Glioblastoma multiforme	21080181	CNVD
Sudden cardiac death	19188705	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	21952639	CNVD
Disorders of sex development	21048976	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
abnormal development	18461090	CNVD
Honadal dysgenesis	21048976	CNVD
Medulloblastoma	21979893	CNVD
Lung cancer	16740712	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Oral squamous cell carcinoma	17134496	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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Developmental delay	21147756	CNVD
Lung cancer	18438408	CNVD
XY gonadal dysgenesis	20685758	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Hepatocellular carcinoma	18803288	CNVD
Breast cancer	21364760	CNVD
Metastatic melanoma	18483359	CNVD
Glioblastoma	19074898	CNVD
Malignant melanoma	19074898	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Medulloblastoma	16783165	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Schizophrenia	23813976	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD

Chromatin state (count:426 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:6789000-6831800	Weak transcription	Osteobl	bone
2	chr9:6789200-6834200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr9:6789200-6834400	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr9:6792000-6831400	Weak transcription	Fetal Muscle Trunk	muscle
5	chr9:6793200-6834400	Weak transcription	Ovary	ovary
6	chr9:6794400-6834600	Weak transcription	Right Ventricle	heart
7	chr9:6794600-6831600	Weak transcription	HSMMtube	muscle
8	chr9:6794800-6834200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr9:6795000-6863800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
10	chr9:6795400-6849600	Weak transcription	HMEC	breast
11	chr9:6799600-6834400	Weak transcription	Spleen	Spleen
12	chr9:6806000-6831600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr9:6806000-6834600	Weak transcription	Brain Angular Gyrus	brain
14	chr9:6806200-6828800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr9:6806800-6834600	Weak transcription	Fetal Muscle Leg	muscle
16	chr9:6806800-6834600	Weak transcription	Rectal Smooth Muscle	rectum
17	chr9:6807000-6831600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr9:6807000-6834200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr9:6807200-6831600	Weak transcription	Fetal Stomach	stomach
20	chr9:6807800-6831400	Weak transcription	Thymus	Thymus
21	chr9:6814400-6833600	Weak transcription	NHLF	lung
22	chr9:6814600-6845400	Weak transcription	Fetal Brain Male	brain
23	chr9:6815400-6852000	Weak transcription	NHDF-Ad	bronchial
24	chr9:6815800-6831200	Weak transcription	Cortex derived primary cultured neurospheres	brain
25	chr9:6816000-6830800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr9:6816000-6856000	Weak transcription	Colon Smooth Muscle	Colon
27	chr9:6818800-6834200	Weak transcription	Pancreas	Pancrea
28	chr9:6818800-6856000	Weak transcription	Psoas Muscle	Psoas
29	chr9:6819600-6834400	Weak transcription	Brain Substantia Nigra	brain
30	chr9:6819800-6829200	Weak transcription	Pancreatic Islets	Pancreatic Islet
31	chr9:6819800-6853400	Weak transcription	Small Intestine	intestine
32	chr9:6820200-6834600	Weak transcription	H9 Cell Line	embryonic stem cell
33	chr9:6820400-6829000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr9:6820400-6829200	Weak transcription	K562	blood
35	chr9:6820400-6834000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr9:6820400-6845200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr9:6820600-6829200	Weak transcription	Fetal Intestine Small	intestine
38	chr9:6820600-6832200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
39	chr9:6820600-6834400	Weak transcription	HUES48 Cell Line	embryonic stem cell
40	chr9:6820600-6834400	Weak transcription	Colonic Mucosa	Colon
41	chr9:6820600-6834400	Weak transcription	Fetal Intestine Large	intestine
42	chr9:6822800-6832000	Strong transcription	Primary B cells from cord blood	blood
43	chr9:6823000-6831600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
44	chr9:6823200-6828800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
45	chr9:6823200-6834400	Weak transcription	Skeletal Muscle Male	skeletal muscle
46	chr9:6823400-6834400	Weak transcription	Skeletal Muscle Female	skeletal muscle
47	chr9:6823600-6834200	Weak transcription	Esophagus	oesophagus
48	chr9:6823800-6831400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr9:6823800-6834200	Weak transcription	Gastric	stomach
50	chr9:6824000-6828800	Weak transcription	NHEK	skin

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