Variant report

Variant	nsv892653
Chromosome Location	chr9:16848790-16895610
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	BACH1	chr9:16870940-16871146	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr9:16870063-16870262	H1-hESC	embryonic stem cell:	n/a	n/a
3	BRCA1	chr9:16870026-16870092	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr9:16873182-16873748	IMR90	lung:	n/a	chr9:16873434-16873445
5	CEBPB	chr9:16868060-16868408	A549	lung:	n/a	chr9:16868232-16868241 chr9:16868232-16868243 chr9:16868230-16868241
6	CEBPB	chr9:16873229-16873384	A549	lung:	n/a	n/a
7	CEBPB	chr9:16865182-16865443	IMR90	lung:	n/a	n/a
8	CEBPB	chr9:16867953-16868427	IMR90	lung:	n/a	chr9:16868232-16868241 chr9:16868232-16868243 chr9:16868230-16868241
9	CEBPB	chr9:16850699-16850775	Hela-S3	cervix:	n/a	chr9:16850746-16850757
10	CEBPB	chr9:16867927-16868542	A549	lung:	n/a	chr9:16868232-16868241 chr9:16868232-16868243 chr9:16868230-16868241
11	CEBPB	chr9:16850629-16850828	H1-hESC	embryonic stem cell:	n/a	chr9:16850746-16850757
12	CEBPB	chr9:16870607-16870634	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr9:16849320-16849487	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr9:16880221-16880332	H1-hESC	embryonic stem cell:	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	chr9:16885265-16885574	Hela-S3	cervix:	n/a	chr9:16885528-16885541
17	CEBPB	chr9:16868029-16868431	Hela-S3	cervix:	n/a	chr9:16868232-16868241 chr9:16868232-16868243 chr9:16868230-16868241
18	CEBPB	chr9:16868064-16868414	HepG2	liver:	n/a	chr9:16868232-16868241 chr9:16868232-16868243 chr9:16868230-16868241
19	CEBPB	chr9:16850582-16850900	A549	lung:	n/a	chr9:16850746-16850757
20	CEBPB	chr9:16868049-16868429	ECC-1	luminal epithelium:	n/a	chr9:16868232-16868241 chr9:16868232-16868243 chr9:16868230-16868241
21	CEBPB	chr9:16868041-16868355	ECC-1	luminal epithelium:	n/a	chr9:16868232-16868241 chr9:16868232-16868243 chr9:16868230-16868241
22	CEBPB	chr9:16873187-16873697	Hela-S3	cervix:	n/a	chr9:16873434-16873445
23	CEBPB	chr9:16850597-16850910	IMR90	lung:	n/a	chr9:16850746-16850757
24	CEBPB	chr9:16868014-16868463	A549	lung:	n/a	chr9:16868232-16868241 chr9:16868232-16868243 chr9:16868230-16868241
25	CEBPB	chr9:16868084-16868399	H1-hESC	embryonic stem cell:	n/a	chr9:16868232-16868241 chr9:16868232-16868243 chr9:16868230-16868241
26	CEBPB	chr9:16884994-16885796	IMR90	lung:	n/a	chr9:16885528-16885541
27	CEBPB	chr9:16850575-16850932	HepG2	liver:	n/a	chr9:16850746-16850757
28	CHD1	chr9:16869619-16870710	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD1	chr9:16871612-16872256	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD1	chr9:16871061-16871345	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr9:16871622-16871908	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr9:16870873-16871230	H1-hESC	embryonic stem cell:	n/a	chr9:16871004-16871014
33	CREB1	chr9:16870578-16870957	A549	lung:	n/a	n/a
34	CTBP2	chr9:16869579-16870832	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr9:16866720-16866870	AoAF	blood vessel:	n/a	n/a
36	CTCF	chr9:16870643-16870750	ProgFib	skin:	n/a	n/a
37	CTCF	chr9:16870480-16870630	HRPEpiC	eye:	n/a	n/a
38	CTCF	chr9:16871980-16872130	AG09319	gingival:	n/a	n/a
39	CTCF	chr9:16871876-16871955	Gliobla	brain:	n/a	n/a
40	CTCF	chr9:16870600-16870750	HBMEC	blood vessel:	n/a	n/a
41	CTCF	chr9:16870640-16870790	HA-sp	spinal cord:	n/a	n/a
42	CTCF	chr9:16870620-16870770	HRPEpiC	eye:	n/a	n/a
43	CTCF	chr9:16870600-16870750	AG04450	lung:	n/a	n/a
44	CTCF	chr9:16870480-16870630	RPTEC	kidney:	n/a	n/a
45	CTCF	chr9:16866840-16866990	HVMF	connective:	n/a	n/a
46	CTCF	chr9:16871800-16871950	HPF	lung:	n/a	n/a
47	CTCF	chr9:16871920-16872070	HCM	heart:	n/a	n/a
48	CTCF	chr9:16873140-16873290	Caco-2	colon:	n/a	n/a
49	CTCF	chr9:16870680-16870830	NHLF	lung:	n/a	n/a
50	CTCF	chr9:16870600-16870750	HA-sp	spinal cord:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:16871106-16871156	HMEC	breast:	n/a
2	chr9:16871106-16871156	HMEC	breast:	n/a
3	chr9:16871106-16871156	HEEpiC	esophagus:	n/a
4	chr9:16870893-16870943	GM12878	blood:	n/a
5	chr9:16870893-16870943	HL-60	blood:	n/a
6	chr9:16871106-16871156	HEK293	kidney:	embryo
7	chr9:16871185-16871235	NHDF-neo	bronchial:	n/a
8	chr9:16864746-16864796	HCM	heart:	n/a
9	chr9:16868891-16868941	AG09319	gingival:	n/a
10	chr9:16870464-16870514	AG09319	gingival:	n/a
11	chr9:16864746-16864796	AG04449	skin:	fetal
12	chr9:16872192-16872242	BJ	skin:	n/a
13	chr9:16872192-16872242	HEEpiC	esophagus:	n/a
14	chr9:16872192-16872242	Jurkat	blood:	n/a
15	chr9:16864746-16864796	Caco-2	colon:	n/a
16	chr9:16872192-16872242	AG04450	lung:	fetal
17	chr9:16871185-16871235	AG09319	gingival:	n/a
18	chr9:16871185-16871235	AG09309	skin:	n/a
19	chr9:16871185-16871235	AoSMC	blood vessel:	n/a
20	chr9:16871185-16871235	HepG2	liver:	n/a
21	chr9:16872192-16872242	H1-hESC	embryonic stem cell:	embryo
22	chr9:16871185-16871235	NH-A	brain:	n/a
23	chr9:16870893-16870943	HNPCEpiC	eye:	n/a
24	chr9:16868891-16868941	Caco-2	colon:	n/a
25	chr9:16870289-16870339	HIPEpiC	eye:	n/a
26	chr9:16875612-16875662	H1-hESC	embryonic stem cell:	embryo
27	chr9:16870289-16870339	NB4	blood:	n/a
28	chr9:16870091-16870141	NHBE	bronchial:	n/a
29	chr9:16871185-16871235	SKMC	muscle:	n/a
30	chr9:16870893-16870943	A549	lung:	n/a
31	chr9:16868891-16868941	BE2_C	brain:	n/a
32	chr9:16875612-16875662	ProgFib	skin:	n/a
33	chr9:16875612-16875662	HNPCEpiC	eye:	n/a
34	chr9:16875612-16875662	GM12891	blood:	n/a
35	chr9:16872192-16872242	HNPCEpiC	eye:	n/a
36	chr9:16870289-16870339	SK-N-MC	brain:	n/a
37	chr9:16870289-16870339	Caco-2	colon:	n/a
38	chr9:16870091-16870141	AG04450	lung:	fetal
39	chr9:16871106-16871156	IMR90	lung:	fetal
40	chr9:16871106-16871156	NH-A	brain:	n/a
41	chr9:16870464-16870514	IMR90	lung:	fetal
42	chr9:16872192-16872242	HCM	heart:	n/a
43	chr9:16868891-16868941	Hela-S3	cervix:	n/a
44	chr9:16875612-16875662	AG09319	gingival:	n/a
45	chr9:16872192-16872242	Hela-S3	cervix:	n/a
46	chr9:16864746-16864796	IMR90	lung:	fetal
47	chr9:16870091-16870141	HEEpiC	esophagus:	n/a
48	chr9:16871106-16871156	PrEC	prostate:	n/a
49	chr9:16870893-16870943	NB4	blood:	n/a
50	chr9:16870464-16870514	AoSMC	blood vessel:	n/a

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

Extended variants
information (count: 2222 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:2222 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1339552	chr9:16848790-16848791	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs141168576	chr9:16848831-16848832	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs554345807	chr9:16848862-16848863	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs113319499	chr9:16848867-16848868	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs139379110	chr9:16848902-16848903	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs191730266	chr9:16848911-16848912	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs184280199	chr9:16848957-16848958	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs188962644	chr9:16848984-16848985	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs78059686	chr9:16849032-16849033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs556038474	chr9:16849038-16849039	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs577521405	chr9:16849039-16849040	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs544836771	chr9:16849045-16849046	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs376224217	chr9:16849051-16849052	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs192224084	chr9:16849067-16849068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs527368353	chr9:16849158-16849159	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs185400796	chr9:16849192-16849193	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs114384002	chr9:16849200-16849201	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs141722515	chr9:16849208-16849209	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs531323067	chr9:16849229-16849230	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs7039999	chr9:16849248-16849249	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs571922222	chr9:16849326-16849327	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs532862208	chr9:16849330-16849331	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs35561834	chr9:16849374-16849375	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs143773454	chr9:16849389-16849390	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs190649218	chr9:16849416-16849417	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs148103261	chr9:16849459-16849460	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs10962640	chr9:16849464-16849465	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs569865061	chr9:16849471-16849472	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs537003449	chr9:16849490-16849491	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs558540299	chr9:16849492-16849493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs141894964	chr9:16849502-16849503	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs545309755	chr9:16849506-16849507	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs555440331	chr9:16849511-16849512	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs373804355	chr9:16849513-16849514	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs12685962	chr9:16849517-16849518	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs533060152	chr9:16849518-16849519	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs138716343	chr9:16849535-16849536	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs10962641	chr9:16849604-16849605	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs543399954	chr9:16849627-16849628	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs564887504	chr9:16849635-16849636	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs182325731	chr9:16849637-16849638	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs80023160	chr9:16849647-16849648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs566287920	chr9:16849693-16849694	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs375080293	chr9:16849714-16849715	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs10481508	chr9:16849720-16849721	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs548502651	chr9:16849727-16849728	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs565403361	chr9:16849748-16849749	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs569776506	chr9:16849762-16849763	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs186044108	chr9:16849778-16849779	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs117570235	chr9:16849853-16849854	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:895 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:16829200-16852800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr9:16829800-16864200	Weak transcription	NH-A	brain
3	chr9:16831000-16859600	Weak transcription	HSMM	muscle
4	chr9:16831200-16852600	Weak transcription	Fetal Lung	lung
5	chr9:16831200-16863400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr9:16831200-16864400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr9:16833800-16863800	Weak transcription	NHLF	lung
8	chr9:16834600-16852600	Weak transcription	Fetal Stomach	stomach
9	chr9:16836200-16864400	Weak transcription	NHDF-Ad	bronchial
10	chr9:16838800-16852000	Weak transcription	Muscle Satellite Cultured Cells	--
11	chr9:16840400-16852000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr9:16840600-16849400	Weak transcription	Ovary	ovary
13	chr9:16842200-16852000	Weak transcription	Colon Smooth Muscle	Colon
14	chr9:16843000-16853200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr9:16843400-16850600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr9:16845200-16849600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
17	chr9:16846000-16851200	Weak transcription	Fetal Muscle Leg	muscle
18	chr9:16846600-16852000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr9:16846600-16852800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr9:16848000-16849400	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr9:16848200-16849000	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr9:16848400-16848800	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr9:16848400-16852800	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr9:16848600-16852000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr9:16848600-16852600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr9:16848600-16852800	Weak transcription	H1 Cell Line	embryonic stem cell
27	chr9:16848800-16852400	Weak transcription	HUES48 Cell Line	embryonic stem cell
28	chr9:16849000-16852600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
29	chr9:16849400-16849800	Enhancers	Ovary	ovary
30	chr9:16849400-16852400	Weak transcription	HUES64 Cell Line	embryonic stem cell
31	chr9:16849600-16849800	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr9:16849800-16850200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
33	chr9:16849800-16850600	Weak transcription	Ovary	ovary
34	chr9:16850200-16850400	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr9:16850400-16852400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
36	chr9:16850600-16850800	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr9:16850600-16851000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr9:16850600-16851600	Enhancers	Ovary	ovary
39	chr9:16850800-16852600	Weak transcription	HUES6 Cell Line	embryonic stem cell
40	chr9:16851000-16851800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr9:16851600-16852600	Weak transcription	Ovary	ovary
42	chr9:16851800-16854200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr9:16852000-16852800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr9:16852000-16853000	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr9:16852000-16853400	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr9:16852000-16853400	Enhancers	Colon Smooth Muscle	Colon
47	chr9:16852400-16852800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr9:16852400-16853200	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr9:16852400-16853200	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr9:16852400-16853200	Enhancers	HUES64 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links