Variant report

Variant	nsv892651
Chromosome Location	chr9:16816755-16869240
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	CEBPB	chr9:16868049-16868429	ECC-1	luminal epithelium:	n/a	chr9:16868232-16868241 chr9:16868232-16868243 chr9:16868230-16868241
2	CEBPB	chr9:16867953-16868427	IMR90	lung:	n/a	chr9:16868232-16868241 chr9:16868232-16868243 chr9:16868230-16868241
3	CEBPB	chr9:16850699-16850775	Hela-S3	cervix:	n/a	chr9:16850746-16850757
4	CEBPB	chr9:16868041-16868355	ECC-1	luminal epithelium:	n/a	chr9:16868232-16868241 chr9:16868232-16868243 chr9:16868230-16868241
5	CEBPB	chr9:16850575-16850932	HepG2	liver:	n/a	chr9:16850746-16850757
6	CEBPB	chr9:16839182-16839183	A549	lung:	n/a	n/a
7	CEBPB	chr9:16868060-16868408	A549	lung:	n/a	chr9:16868232-16868241 chr9:16868232-16868243 chr9:16868230-16868241
8	CEBPB	chr9:16868014-16868463	A549	lung:	n/a	chr9:16868232-16868241 chr9:16868232-16868243 chr9:16868230-16868241
9	CEBPB	chr9:16850582-16850900	A549	lung:	n/a	chr9:16850746-16850757
10	CEBPB	chr9:16850597-16850910	IMR90	lung:	n/a	chr9:16850746-16850757
11	CEBPB	chr9:16849320-16849487	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr9:16850629-16850828	H1-hESC	embryonic stem cell:	n/a	chr9:16850746-16850757
13	CEBPB	chr9:16867927-16868542	A549	lung:	n/a	chr9:16868232-16868241 chr9:16868232-16868243 chr9:16868230-16868241
14	CEBPB	chr9:16825716-16826574	IMR90	lung:	n/a	n/a
15	CEBPB	chr9:16868073-16868432	MCF-7	breast:	n/a	chr9:16868232-16868241 chr9:16868232-16868243 chr9:16868230-16868241
16	CEBPB	chr9:16838887-16839367	IMR90	lung:	n/a	n/a
17	CEBPB	chr9:16868029-16868431	Hela-S3	cervix:	n/a	chr9:16868232-16868241 chr9:16868232-16868243 chr9:16868230-16868241
18	CEBPB	chr9:16868084-16868399	H1-hESC	embryonic stem cell:	n/a	chr9:16868232-16868241 chr9:16868232-16868243 chr9:16868230-16868241
19	CEBPB	chr9:16868064-16868414	HepG2	liver:	n/a	chr9:16868232-16868241 chr9:16868232-16868243 chr9:16868230-16868241
20	CEBPB	chr9:16865182-16865443	IMR90	lung:	n/a	n/a
21	CEBPB	chr9:16848154-16848536	ECC-1	luminal epithelium:	n/a	n/a
22	CEBPB	chr9:16839177-16839212	Hela-S3	cervix:	n/a	n/a
23	CTCF	chr9:16824980-16825130	A549	lung:	n/a	n/a
24	CTCF	chr9:16866780-16866930	HCFaa	heart:	n/a	n/a
25	CTCF	chr9:16824840-16824990	HFF-Myc	foreskin:	n/a	chr9:16824960-16824978 chr9:16824963-16824973 chr9:16824955-16824976
26	CTCF	chr9:16866720-16866870	RPTEC	kidney:	n/a	n/a
27	CTCF	chr9:16824899-16825004	A549	lung:	n/a	chr9:16824960-16824978 chr9:16824963-16824973 chr9:16824955-16824976
28	CTCF	chr9:16866800-16866950	HCM	heart:	n/a	n/a
29	CTCF	chr9:16824840-16824990	HVMF	connective:	n/a	chr9:16824960-16824978 chr9:16824963-16824973 chr9:16824955-16824976
30	CTCF	chr9:16856502-16856536	Kidney_OC	kidney:	n/a	n/a
31	CTCF	chr9:16864520-16864670	HMF	breast:	n/a	n/a
32	CTCF	chr9:16824900-16825050	NHDF-neo	bronchial:	n/a	chr9:16824960-16824978 chr9:16824963-16824973 chr9:16824955-16824976
33	CTCF	chr9:16824920-16825070	GM06990	blood:	n/a	chr9:16824960-16824978 chr9:16824963-16824973 chr9:16824955-16824976
34	CTCF	chr9:16824860-16825010	AG09319	gingival:	n/a	chr9:16824960-16824978 chr9:16824963-16824973 chr9:16824955-16824976
35	CTCF	chr9:16866760-16866910	NHLF	lung:	n/a	n/a
36	CTCF	chr9:16828600-16828750	SK-N-SH_RA	brain:	n/a	n/a
37	CTCF	chr9:16866740-16866890	HMF	breast:	n/a	n/a
38	CTCF	chr9:16866740-16866890	HAc	cerebellar:	n/a	n/a
39	CTCF	chr9:16824860-16825010	BJ	skin:	n/a	chr9:16824960-16824978 chr9:16824963-16824973 chr9:16824955-16824976
40	CTCF	chr9:16824820-16824970	HCPEpiC	choroid plexus:	n/a	n/a
41	CTCF	chr9:16824860-16825010	HPF	lung:	n/a	chr9:16824960-16824978 chr9:16824963-16824973 chr9:16824955-16824976
42	CTCF	chr9:16824560-16824710	NHEK	skin:	n/a	n/a
43	CTCF	chr9:16824940-16825090	AG09319	gingival:	n/a	chr9:16824960-16824978 chr9:16824963-16824973 chr9:16824955-16824976
44	CTCF	chr9:16866700-16866850	AoAF	blood vessel:	n/a	n/a
45	CTCF	chr9:16866780-16866930	AG09319	gingival:	n/a	n/a
46	CTCF	chr9:16824780-16824930	AG04450	lung:	n/a	n/a
47	CTCF	chr9:16824900-16825050	BJ	skin:	n/a	chr9:16824960-16824978 chr9:16824963-16824973 chr9:16824955-16824976
48	CTCF	chr9:16824860-16825010	AG09309	skin:	n/a	chr9:16824960-16824978 chr9:16824963-16824973 chr9:16824955-16824976
49	CTCF	chr9:16866780-16866930	AG04449	skin:	n/a	n/a
50	CTCF	chr9:16824887-16825018	NHEK	skin:	n/a	chr9:16824960-16824978 chr9:16824963-16824973 chr9:16824955-16824976

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:16868891-16868941	NT2-D1	testis:	n/a
2	chr9:16868891-16868941	NT2-D1	testis:	n/a
3	chr9:16829168-16829218	HL-60	blood:	n/a
4	chr9:16868891-16868941	AG04449	skin:	fetal
5	chr9:16829168-16829218	IMR90	lung:	fetal
6	chr9:16829168-16829218	ProgFib	skin:	n/a
7	chr9:16868891-16868941	HEEpiC	esophagus:	n/a
8	chr9:16864746-16864796	PrEC	prostate:	n/a
9	chr9:16868891-16868941	LNCaP	prostate:	n/a
10	chr9:16868891-16868941	HMEC	breast:	n/a
11	chr9:16829168-16829218	Jurkat	blood:	n/a
12	chr9:16868891-16868941	BE2_C	brain:	n/a
13	chr9:16829168-16829218	HNPCEpiC	eye:	n/a
14	chr9:16868891-16868941	AG10803	skin:	n/a
15	chr9:16868891-16868941	GM19239	blood:	n/a
16	chr9:16864746-16864796	ECC-1	luminal epithelium:	n/a
17	chr9:16829168-16829218	T-47D	breast:	n/a
18	chr9:16864746-16864796	BJ	skin:	n/a
19	chr9:16864746-16864796	HNPCEpiC	eye:	n/a
20	chr9:16864746-16864796	PFSK-1	brain:	n/a
21	chr9:16864746-16864796	BE2_C	brain:	n/a
22	chr9:16864746-16864796	CMK	blood:	n/a
23	chr9:16864746-16864796	Caco-2	colon:	n/a
24	chr9:16868891-16868941	GM06990	blood:	n/a
25	chr9:16864746-16864796	Hela-S3	cervix:	n/a
26	chr9:16868891-16868941	HPAEpiC	pulmonary alveolar:	n/a
27	chr9:16864746-16864796	HAEpiC	amniotic membrane:	n/a
28	chr9:16868891-16868941	HRE	kidney:	n/a
29	chr9:16868891-16868941	AG04450	lung:	fetal
30	chr9:16829168-16829218	SK-N-MC	brain:	n/a
31	chr9:16864746-16864796	HMEC	breast:	n/a
32	chr9:16864746-16864796	NHDF-neo	bronchial:	n/a
33	chr9:16829168-16829218	PFSK-1	brain:	n/a
34	chr9:16868891-16868941	ovcar-3	ovarian:	n/a
35	chr9:16868891-16868941	GM12878	blood:	n/a
36	chr9:16864746-16864796	HCPEpiC	choroid plexus:	n/a
37	chr9:16864746-16864796	HepG2	liver:	n/a
38	chr9:16829168-16829218	AG04450	lung:	fetal
39	chr9:16868891-16868941	SK-N-SH	brain:	n/a
40	chr9:16829168-16829218	SAEC	small airway:	n/a
41	chr9:16829168-16829218	HCF	heart:	n/a
42	chr9:16868891-16868941	K562	blood:	n/a
43	chr9:16829168-16829218	MCF10A-Er-Src	breast:	n/a
44	chr9:16864746-16864796	HRE	kidney:	n/a
45	chr9:16829168-16829218	PANC-1	pancreas:	n/a
46	chr9:16868891-16868941	HCT-116	colon:	n/a
47	chr9:16864746-16864796	Jurkat	blood:	n/a
48	chr9:16829168-16829218	AG04449	skin:	fetal
49	chr9:16868891-16868941	HUVEC	blood vessel:	n/a
50	chr9:16864746-16864796	HEEpiC	esophagus:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:16833151..16834904-chr9:16839778..16842584,2	MCF-7	breast:
2	chr9:16833151..16834904-chr9:16839778..16842584,2	MCF-7	breast:

Variant related genes	Relation type
BNC2	TF binding region
BNC2	CpG island

Extended variants
information (count: 2588 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:2588 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3936215	chr9:16816755-16816756	Enhancers Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs560530233	chr9:16816774-16816775	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs148715193	chr9:16816777-16816778	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs540486576	chr9:16816789-16816790	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs561988388	chr9:16816823-16816824	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs529066605	chr9:16816832-16816833	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs544406634	chr9:16816844-16816845	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs562571676	chr9:16816913-16816914	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs142292356	chr9:16817018-16817019	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs188858123	chr9:16817027-16817028	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs551226654	chr9:16817052-16817053	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs367739363	chr9:16817074-16817075	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs568103367	chr9:16817113-16817114	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs193230781	chr9:16817123-16817124	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs35662925	chr9:16817131-16817132	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs117865972	chr9:16817153-16817154	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs549236742	chr9:16817160-16817161	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs185301694	chr9:16817231-16817232	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs17743789	chr9:16817233-16817234	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs556694918	chr9:16817254-16817255	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs571789635	chr9:16817265-16817266	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs139424536	chr9:16817266-16817267	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs189034645	chr9:16817273-16817274	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs112742327	chr9:16817285-16817286	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs531276188	chr9:16817327-16817328	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs563911895	chr9:16817362-16817363	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs572444098	chr9:16817424-16817425	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs543062229	chr9:16817452-16817453	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs555040293	chr9:16817464-16817465	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs573963042	chr9:16817484-16817485	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs544566884	chr9:16817492-16817493	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs562692743	chr9:16817508-16817509	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs181427204	chr9:16817552-16817553	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs144074421	chr9:16817566-16817567	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs111434375	chr9:16817588-16817589	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs371300603	chr9:16817611-16817612	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs567904001	chr9:16817708-16817709	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs55933102	chr9:16817720-16817721	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs548554274	chr9:16817818-16817819	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs371156966	chr9:16817877-16817878	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs374441611	chr9:16817950-16817951	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs562488664	chr9:16817957-16817958	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs566950078	chr9:16817962-16817963	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs547141911	chr9:16817968-16817969	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs550216822	chr9:16818001-16818002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs566878769	chr9:16818010-16818011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs543656320	chr9:16818018-16818019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs571766466	chr9:16818025-16818026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs538883150	chr9:16818125-16818126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs554207155	chr9:16818139-16818140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

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
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
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Myelofibrosis	22110671	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
Breast cancer	21611746	CNVD
Pancreatic cancer	21811587	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1026 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:16796200-16816800	Weak transcription	HSMMtube	muscle
2	chr9:16796400-16824400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr9:16810600-16817200	Weak transcription	Stomach Smooth Muscle	stomach
4	chr9:16810600-16824400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr9:16810600-16824400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr9:16810800-16817200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr9:16810800-16824200	Weak transcription	HSMM	muscle
8	chr9:16812200-16824400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr9:16812600-16823800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr9:16812600-16826200	Weak transcription	Duodenum Smooth Muscle	Duodenum
11	chr9:16812800-16824600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr9:16814200-16817200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr9:16814200-16817600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr9:16814200-16817600	Weak transcription	Osteobl	bone
15	chr9:16814200-16824000	Weak transcription	NHLF	lung
16	chr9:16814400-16824200	Weak transcription	Muscle Satellite Cultured Cells	--
17	chr9:16814600-16817800	Enhancers	Rectal Smooth Muscle	rectum
18	chr9:16814800-16817200	Enhancers	Fetal Stomach	stomach
19	chr9:16814800-16817800	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr9:16814800-16818000	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr9:16815200-16817800	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr9:16815400-16816800	Enhancers	Fetal Kidney	kidney
23	chr9:16815400-16817000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr9:16815400-16817600	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr9:16815400-16817800	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr9:16815400-16822200	Weak transcription	Fetal Lung	lung
27	chr9:16815600-16817800	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr9:16815800-16817400	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr9:16816000-16817800	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr9:16816000-16817800	Enhancers	H9 Cell Line	embryonic stem cell
31	chr9:16816200-16817400	Enhancers	Ovary	ovary
32	chr9:16816200-16818000	Enhancers	Colon Smooth Muscle	Colon
33	chr9:16816600-16816800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
34	chr9:16816600-16817000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr9:16816600-16817800	Enhancers	H1 Cell Line	embryonic stem cell
36	chr9:16816800-16817200	Enhancers	HSMMtube	muscle
37	chr9:16817000-16817800	Enhancers	NHDF-Ad	bronchial
38	chr9:16817000-16823400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr9:16817200-16817400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr9:16817200-16817400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr9:16817200-16817800	Enhancers	Stomach Smooth Muscle	stomach
42	chr9:16817200-16824400	Weak transcription	Fetal Stomach	stomach
43	chr9:16817200-16824400	Weak transcription	HSMMtube	muscle
44	chr9:16817400-16818000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr9:16817400-16824400	Weak transcription	Ovary	ovary
46	chr9:16817400-16824600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr9:16817600-16817800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr9:16817600-16817800	Enhancers	Osteobl	bone
49	chr9:16817600-16822200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
50	chr9:16817800-16818000	Weak transcription	Stomach Smooth Muscle	stomach

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