Variant report

Variant	nsv430000
Chromosome Location	chr9:16603483-16671045
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	chr9:16653619-16654168	HepG2	liver:	n/a	n/a
2	ATF3	chr9:16626544-16626978	A549	lung:	n/a	n/a
3	BACH1	chr9:16626901-16626943	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr9:16655674-16655965	GM12878	blood:	n/a	chr9:16655674-16655683 chr9:16655674-16655683 chr9:16655675-16655684
5	BRCA1	chr9:16623666-16623719	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr9:16611997-16612266	HepG2	liver:	n/a	chr9:16612112-16612121 chr9:16612110-16612123 chr9:16612110-16612121 chr9:16612111-16612122
7	CEBPB	chr9:16625871-16626165	IMR90	lung:	n/a	n/a
8	CEBPB	chr9:16651134-16651299	IMR90	lung:	n/a	n/a
9	CEBPB	chr9:16618569-16618849	Hela-S3	cervix:	n/a	chr9:16618703-16618716 chr9:16618705-16618714 chr9:16618705-16618714 chr9:16618705-16618714 chr9:16618703-16618716 chr9:16618705-16618716 chr9:16618705-16618714 chr9:16618703-16618714
10	CEBPB	chr9:16647398-16647660	A549	lung:	n/a	chr9:16647524-16647533 chr9:16647522-16647533 chr9:16647524-16647535
11	CEBPB	chr9:16618528-16618899	IMR90	lung:	n/a	chr9:16618703-16618716 chr9:16618705-16618714 chr9:16618705-16618714 chr9:16618705-16618714 chr9:16618703-16618716 chr9:16618705-16618716 chr9:16618705-16618714 chr9:16618703-16618714
12	CEBPB	chr9:16611983-16612143	H1-hESC	embryonic stem cell:	n/a	chr9:16612112-16612121 chr9:16612110-16612123 chr9:16612110-16612121 chr9:16612111-16612122
13	CEBPB	chr9:16647375-16647679	HepG2	liver:	n/a	chr9:16647524-16647533 chr9:16647522-16647533 chr9:16647524-16647535
14	CEBPB	chr9:16618576-16618869	A549	lung:	n/a	chr9:16618703-16618716 chr9:16618705-16618714 chr9:16618705-16618714 chr9:16618705-16618714 chr9:16618703-16618716 chr9:16618705-16618716 chr9:16618705-16618714 chr9:16618703-16618714
15	CEBPB	chr9:16634440-16634631	IMR90	lung:	n/a	n/a
16	CEBPB	chr9:16618652-16618889	H1-hESC	embryonic stem cell:	n/a	chr9:16618703-16618716 chr9:16618705-16618714 chr9:16618705-16618714 chr9:16618705-16618714 chr9:16618703-16618716 chr9:16618705-16618716 chr9:16618705-16618714 chr9:16618703-16618714
17	CEBPB	chr9:16611999-16612294	A549	lung:	n/a	chr9:16612112-16612121 chr9:16612110-16612123 chr9:16612110-16612121 chr9:16612111-16612122
18	CEBPB	chr9:16611944-16612311	IMR90	lung:	n/a	chr9:16612112-16612121 chr9:16612110-16612123 chr9:16612110-16612121 chr9:16612111-16612122
19	CEBPB	chr9:16626665-16626979	IMR90	lung:	n/a	chr9:16626932-16626944
20	CEBPB	chr9:16654726-16654923	H1-hESC	embryonic stem cell:	n/a	chr9:16654879-16654892
21	CEBPB	chr9:16654849-16654963	A549	lung:	n/a	chr9:16654879-16654892
22	CEBPB	chr9:16654727-16655039	IMR90	lung:	n/a	chr9:16654879-16654892
23	CEBPB	chr9:16647342-16647662	IMR90	lung:	n/a	chr9:16647524-16647533 chr9:16647522-16647533 chr9:16647524-16647535
24	CEBPB	chr9:16618522-16618887	HepG2	liver:	n/a	chr9:16618703-16618716 chr9:16618705-16618714 chr9:16618705-16618714 chr9:16618705-16618714 chr9:16618703-16618716 chr9:16618705-16618716 chr9:16618705-16618714 chr9:16618703-16618714
25	CHD2	chr9:16626657-16626839	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD2	chr9:16628040-16628219	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr9:16605617-16605641	GM12878	blood:	n/a	n/a
28	CHD2	chr9:16628194-16628207	GM12878	blood:	n/a	n/a
29	CTCF	chr9:16640800-16640950	NHLF	lung:	n/a	n/a
30	CTCF	chr9:16640760-16640910	HPAF	blood vessel:	n/a	n/a
31	CTCF	chr9:16640740-16640890	RPTEC	kidney:	n/a	n/a
32	CTCF	chr9:16640760-16640910	HAc	cerebellar:	n/a	n/a
33	CTCF	chr9:16648760-16648910	SAEC	small airway:	n/a	n/a
34	CTCF	chr9:16640860-16641010	A549	lung:	n/a	n/a
35	CTCF	chr9:16640673-16640908	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr9:16640720-16640870	HBMEC	blood vessel:	n/a	n/a
37	CTCF	chr9:16640820-16640970	HMF	breast:	n/a	n/a
38	CTCF	chr9:16640811-16640896	HUVEC	blood vessel:	n/a	n/a
39	CTCF	chr9:16640758-16640890	MCF-7	breast:	n/a	n/a
40	CTCF	chr9:16640740-16640890	BE2_C	brain:	n/a	n/a
41	CTCF	chr9:16640740-16640890	HRPEpiC	eye:	n/a	n/a
42	CTCF	chr9:16640800-16640950	NHDF-neo	bronchial:	n/a	n/a
43	CTCF	chr9:16648846-16648855	GM13977	blood:	n/a	n/a
44	CTCF	chr9:16640800-16640950	GM12865	blood:	n/a	n/a
45	CTCF	chr9:16640720-16640870	AoAF	blood vessel:	n/a	n/a
46	CTCF	chr9:16640740-16640890	HPAF	blood vessel:	n/a	n/a
47	CTCF	chr9:16640800-16640950	WI-38	lung:	n/a	n/a
48	CTCF	chr9:16640700-16640850	GM12873	blood:	n/a	n/a
49	CTCF	chr9:16666135-16666162	GM20000	blood:	n/a	n/a
50	CTCF	chr9:16653460-16653610	HPAF	blood vessel:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:16653688-16653738	AG09309	skin:	n/a
2	chr9:16653688-16653738	AG10803	skin:	n/a
3	chr9:16653688-16653738	HNPCEpiC	eye:	n/a
4	chr9:16653688-16653738	MCF10A-Er-Src	breast:	n/a
5	chr9:16653688-16653738	ECC-1	luminal epithelium:	n/a
6	chr9:16653688-16653738	H1-hESC	embryonic stem cell:	embryo
7	chr9:16653688-16653738	HMEC	breast:	n/a
8	chr9:16653688-16653738	NHDF-neo	bronchial:	n/a
9	chr9:16653688-16653738	SAEC	small airway:	n/a
10	chr9:16653688-16653738	NB4	blood:	n/a
11	chr9:16653688-16653738	ProgFib	skin:	n/a
12	chr9:16653688-16653738	AG09319	gingival:	n/a
13	chr9:16653688-16653738	PFSK-1	brain:	n/a
14	chr9:16653688-16653738	HRCEpiC	kidney:	n/a
15	chr9:16653688-16653738	GM06990	blood:	n/a
16	chr9:16653688-16653738	IMR90	lung:	fetal
17	chr9:16653688-16653738	Hepatocyte	liver:	n/a
18	chr9:16653688-16653738	U87	brain:	n/a
19	chr9:16653688-16653738	GM19239	blood:	n/a
20	chr9:16653688-16653738	MCF-7	breast:	n/a
21	chr9:16653688-16653738	Hela-S3	cervix:	n/a
22	chr9:16653688-16653738	Jurkat	blood:	n/a
23	chr9:16653688-16653738	RPTEC	kidney:	n/a
24	chr9:16653688-16653738	Caco-2	colon:	n/a
25	chr9:16653688-16653738	HCPEpiC	choroid plexus:	n/a
26	chr9:16653688-16653738	PANC-1	pancreas:	n/a
27	chr9:16653688-16653738	HEEpiC	esophagus:	n/a
28	chr9:16653688-16653738	A549	lung:	n/a
29	chr9:16653688-16653738	GM12892	blood:	n/a
30	chr9:16653688-16653738	HCM	heart:	n/a
31	chr9:16653688-16653738	NHBE	bronchial:	n/a
32	chr9:16653688-16653738	CMK	blood:	n/a
33	chr9:16653688-16653738	GM12891	blood:	n/a
34	chr9:16653688-16653738	K562	blood:	n/a
35	chr9:16653688-16653738	SK-N-SH_RA	brain:	n/a
36	chr9:16653688-16653738	HEK293	kidney:	embryo
37	chr9:16653688-16653738	HIPEpiC	eye:	n/a
38	chr9:16653688-16653738	ovcar-3	ovarian:	n/a
39	chr9:16653688-16653738	HPAEpiC	pulmonary alveolar:	n/a
40	chr9:16653688-16653738	SK-N-SH	brain:	n/a
41	chr9:16653688-16653738	NT2-D1	testis:	n/a
42	chr9:16653688-16653738	NH-A	brain:	n/a
43	chr9:16653688-16653738	HCF	heart:	n/a
44	chr9:16653688-16653738	SK-N-MC	brain:	n/a
45	chr9:16653688-16653738	GM12878	blood:	n/a
46	chr9:16653688-16653738	AoSMC	blood vessel:	n/a
47	chr9:16653688-16653738	HAEpiC	amniotic membrane:	n/a
48	chr9:16653688-16653738	HRPEpiC	eye:	n/a
49	chr9:16653688-16653738	AG04449	skin:	fetal
50	chr9:16653688-16653738	HepG2	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:16191923..16192798-chr9:16648750..16649311,2	MCF-7	breast:
2	chr9:16653386..16655989-chr9:16657272..16659036,2	MCF-7	breast:
3	chr9:16653386..16655989-chr9:16657272..16659036,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CNTLN-3	chr9:16626156-16626388	ENSG00000230694.1
2	lnc-CNTLN-3	chr9:16625674-16625895	ENSG00000230694.1
3	lnc-C9orf92-4	chr9:16665064-16665173	NONHSAT130290

Variant related genes	Relation type
ENSG00000230694	TF binding region
ENSG00000230694	CpG island

Extended variants
information (count: 3176 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:3176 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs113436336	chr9:16603483-16603484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs368590084	chr9:16603494-16603495	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs184344944	chr9:16603504-16603505	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs532081874	chr9:16603512-16603513	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs547974283	chr9:16603532-16603533	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs187694451	chr9:16603533-16603534	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs193111096	chr9:16603544-16603545	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs7032772	chr9:16603557-16603558	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs185560329	chr9:16603578-16603579	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs149477355	chr9:16603676-16603677	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs113847868	chr9:16603737-16603738	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs537030459	chr9:16603742-16603743	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs77061042	chr9:16603769-16603770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs200787401	chr9:16603849-16603850	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs574419431	chr9:16603886-16603887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs201898723	chr9:16603887-16603888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs534760444	chr9:16603889-16603890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs200197611	chr9:16603893-16603894	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs76212898	chr9:16603894-16603895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs7018743	chr9:16603921-16603922	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs572258022	chr9:16603925-16603926	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs201332967	chr9:16603929-16603930	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs542370269	chr9:16603951-16603952	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs542974226	chr9:16603964-16603965	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs189025708	chr9:16603998-16603999	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs576373117	chr9:16604015-16604016	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs55873179	chr9:16604075-16604076	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs10123190	chr9:16604085-16604086	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs62543460	chr9:16604088-16604089	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs181464506	chr9:16604104-16604105	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs184117632	chr9:16604122-16604123	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs559566226	chr9:16604161-16604162	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs112406059	chr9:16604206-16604207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs530209177	chr9:16604218-16604219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs548503851	chr9:16604225-16604226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs376985342	chr9:16604258-16604259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs570028618	chr9:16604271-16604272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs544090657	chr9:16604275-16604276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs188512779	chr9:16604280-16604281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs531081628	chr9:16604291-16604292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs56728579	chr9:16604398-16604399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs552543203	chr9:16604420-16604421	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs570712908	chr9:16604421-16604422	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs535157840	chr9:16604423-16604424	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs553172739	chr9:16604461-16604462	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs79975355	chr9:16604470-16604471	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs565918850	chr9:16604527-16604528	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs536468215	chr9:16604550-16604551	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs181071333	chr9:16604587-16604588	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs138614420	chr9:16604621-16604622	Weak transcription Enhancers Genic enhancers	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
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
Pancreatic ductal adenocarcinoma	19077451	CNVD
early-passage human iPS cells	21368824	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	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1095 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:16583000-16606800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr9:16583200-16611200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr9:16586800-16604400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr9:16595000-16611200	Weak transcription	NHLF	lung
5	chr9:16597600-16604400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr9:16597600-16610800	Weak transcription	Fetal Stomach	stomach
7	chr9:16598800-16608200	Weak transcription	HUES64 Cell Line	embryonic stem cell
8	chr9:16598800-16611400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr9:16599000-16603600	Weak transcription	A549	lung
10	chr9:16599000-16607000	Weak transcription	Colon Smooth Muscle	Colon
11	chr9:16599000-16612200	Weak transcription	Osteobl	bone
12	chr9:16599000-16612600	Weak transcription	HSMM	muscle
13	chr9:16601200-16604200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr9:16602200-16607800	Weak transcription	HUES48 Cell Line	embryonic stem cell
15	chr9:16602400-16608000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
16	chr9:16602600-16608800	Weak transcription	HUES6 Cell Line	embryonic stem cell
17	chr9:16602800-16608600	Weak transcription	Ovary	ovary
18	chr9:16602800-16608800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr9:16602800-16612400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr9:16603200-16612600	Weak transcription	HUVEC	blood vessel
21	chr9:16603600-16603800	Enhancers	A549	lung
22	chr9:16604200-16606600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr9:16604400-16604600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr9:16604400-16604800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr9:16604400-16605000	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr9:16604600-16605600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr9:16604600-16608800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr9:16604800-16606400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr9:16605000-16606800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr9:16605600-16606000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr9:16605600-16607600	Weak transcription	Fetal Lung	lung
32	chr9:16606000-16606200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr9:16606000-16606200	Enhancers	HSMMtube	muscle
34	chr9:16606200-16613600	Weak transcription	HSMMtube	muscle
35	chr9:16606200-16615000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr9:16606400-16607200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr9:16606600-16607400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr9:16606800-16607000	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr9:16606800-16610000	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr9:16607000-16608200	Enhancers	Colon Smooth Muscle	Colon
41	chr9:16607000-16618400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr9:16607200-16609000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr9:16607400-16610200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr9:16607800-16608000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr9:16607800-16608400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr9:16607800-16610000	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr9:16608000-16609000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr9:16608000-16609600	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr9:16608200-16610200	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr9:16608200-16610800	Weak transcription	Colon Smooth Muscle	Colon

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