Variant report

Variant	nsv524954
Chromosome Location	chr9:16432544-16446091
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:120)
CpG islands
(count:61)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:120 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr9:16443222-16443460	A549	lung:	n/a	chr9:16443341-16443352
2	CEBPB	chr9:16445384-16445994	A549	lung:	n/a	n/a
3	CEBPB	chr9:16442629-16443501	Hela-S3	cervix:	n/a	chr9:16443341-16443352 chr9:16443469-16443481 chr9:16443471-16443482
4	CEBPB	chr9:16442663-16442934	A549	lung:	n/a	n/a
5	CEBPB	chr9:16442602-16442930	ECC-1	luminal epithelium:	n/a	n/a
6	CEBPB	chr9:16443202-16443491	HepG2	liver:	n/a	chr9:16443341-16443352 chr9:16443469-16443481 chr9:16443471-16443482
7	CEBPB	chr9:16445516-16445882	IMR90	lung:	n/a	n/a
8	CEBPB	chr9:16445514-16445950	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr9:16445588-16445835	HepG2	liver:	n/a	n/a
10	CEBPB	chr9:16434627-16434842	IMR90	lung:	n/a	n/a
11	CEBPB	chr9:16442560-16443055	A549	lung:	n/a	n/a
12	CEBPB	chr9:16442698-16442978	A549	lung:	n/a	n/a
13	CEBPB	chr9:16445501-16445957	A549	lung:	n/a	n/a
14	CTCF	chr9:16436600-16436750	WERI-Rb-1	eye:	n/a	n/a
15	CTCF	chr9:16436600-16436750	GM12864	blood:	n/a	n/a
16	CTCF	chr9:16436600-16436750	GM12865	blood:	n/a	n/a
17	CTCF	chr9:16436600-16436750	GM12873	blood:	n/a	n/a
18	CTCF	chr9:16436631-16436805	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr9:16436727-16436747	GM12891	blood:	n/a	n/a
20	CTCF	chr9:16436670-16436807	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr9:16436614-16436891	GM12878	blood:	n/a	n/a
22	CTCF	chr9:16436780-16436930	GM12873	blood:	n/a	n/a
23	CTCF	chr9:16436620-16436770	GM12875	blood:	n/a	n/a
24	CTCF	chr9:16436800-16436950	GM06990	blood:	n/a	n/a
25	CTCF	chr9:16436701-16436769	GM12892	blood:	n/a	n/a
26	CTCF	chr9:16436713-16436756	GM19238	blood:	n/a	n/a
27	E2F4	chr9:16445559-16445826	MCF10A-Er-Src	breast:	n/a	n/a
28	EBF1	chr9:16446032-16446085	GM12878	blood:	n/a	n/a
29	ELK4	chr9:16443570-16443765	HEK293	kidney:	n/a	n/a
30	EP300	chr9:16445478-16446072	A549	lung:	n/a	chr9:16445925-16445939
31	EP300	chr9:16445612-16445941	Hela-S3	cervix:	n/a	chr9:16445925-16445939
32	EP300	chr9:16434450-16434652	SK-N-SH_RA	brain:	n/a	chr9:16434510-16434518
33	EP300	chr9:16442417-16443162	ECC-1	luminal epithelium:	n/a	n/a
34	EP300	chr9:16434305-16435060	SK-N-SH	brain:	n/a	chr9:16434510-16434518
35	ESR1	chr9:16442615-16443005	ECC-1	luminal epithelium:	n/a	n/a
36	ESR1	chr9:16442557-16443132	ECC-1	luminal epithelium:	n/a	n/a
37	ESR1	chr9:16442557-16443088	ECC-1	luminal epithelium:	n/a	n/a
38	ESR1	chr9:16442498-16443100	ECC-1	luminal epithelium:	n/a	n/a
39	ESR1	chr9:16442605-16442999	ECC-1	luminal epithelium:	n/a	n/a
40	FOS	chr9:16442639-16443497	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr9:16442660-16443407	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr9:16445609-16445937	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr9:16444069-16444250	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr9:16442379-16443492	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr9:16445553-16445946	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr9:16443258-16443458	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr9:16445496-16446013	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr9:16442011-16443018	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr9:16438944-16439151	MCF10A-Er-Src	breast:	n/a	n/a
50	FOSL2	chr9:16442414-16443101	A549	lung:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:16442831-16442881	NB4	blood:	n/a
2	chr9:16442831-16442881	HRCEpiC	kidney:	n/a
3	chr9:16442831-16442881	HCT-116	colon:	n/a
4	chr9:16442831-16442881	MCF-7	breast:	n/a
5	chr9:16442831-16442881	PFSK-1	brain:	n/a
6	chr9:16442831-16442881	SK-N-SH	brain:	n/a
7	chr9:16442831-16442881	HepG2	liver:	n/a
8	chr9:16442831-16442881	SKMC	muscle:	n/a
9	chr9:16442831-16442881	ProgFib	skin:	n/a
10	chr9:16442831-16442881	GM19239	blood:	n/a
11	chr9:16442831-16442881	AoSMC	blood vessel:	n/a
12	chr9:16442831-16442881	RPTEC	kidney:	n/a
13	chr9:16442831-16442881	GM06990	blood:	n/a
14	chr9:16442831-16442881	Hepatocyte	liver:	n/a
15	chr9:16442831-16442881	NT2-D1	testis:	n/a
16	chr9:16442831-16442881	BE2_C	brain:	n/a
17	chr9:16442831-16442881	HPAEpiC	pulmonary alveolar:	n/a
18	chr9:16442831-16442881	HUVEC	blood vessel:	n/a
19	chr9:16442831-16442881	Hela-S3	cervix:	n/a
20	chr9:16442831-16442881	LNCaP	prostate:	n/a
21	chr9:16442831-16442881	U87	brain:	n/a
22	chr9:16442831-16442881	HNPCEpiC	eye:	n/a
23	chr9:16442831-16442881	SK-N-MC	brain:	n/a
24	chr9:16442831-16442881	NHDF-neo	bronchial:	n/a
25	chr9:16442831-16442881	BJ	skin:	n/a
26	chr9:16442831-16442881	HRE	kidney:	n/a
27	chr9:16442831-16442881	CMK	blood:	n/a
28	chr9:16442831-16442881	AG04449	skin:	fetal
29	chr9:16442831-16442881	T-47D	breast:	n/a
30	chr9:16442831-16442881	AG10803	skin:	n/a
31	chr9:16442831-16442881	PANC-1	pancreas:	n/a
32	chr9:16442831-16442881	HCM	heart:	n/a
33	chr9:16442831-16442881	NHBE	bronchial:	n/a
34	chr9:16442831-16442881	GM12892	blood:	n/a
35	chr9:16442831-16442881	ovcar-3	ovarian:	n/a
36	chr9:16442831-16442881	AG09319	gingival:	n/a
37	chr9:16442831-16442881	K562	blood:	n/a
38	chr9:16442831-16442881	HCPEpiC	choroid plexus:	n/a
39	chr9:16442831-16442881	A549	lung:	n/a
40	chr9:16442831-16442881	GM12878	blood:	n/a
41	chr9:16442831-16442881	ECC-1	luminal epithelium:	n/a
42	chr9:16442831-16442881	MCF10A-Er-Src	breast:	n/a
43	chr9:16442831-16442881	Caco-2	colon:	n/a
44	chr9:16442831-16442881	PrEC	prostate:	n/a
45	chr9:16442831-16442881	HEK293	kidney:	embryo
46	chr9:16442831-16442881	SAEC	small airway:	n/a
47	chr9:16442831-16442881	GM12891	blood:	n/a
48	chr9:16442831-16442881	SK-N-SH_RA	brain:	n/a
49	chr9:16442831-16442881	Jurkat	blood:	n/a
50	chr9:16442831-16442881	HMEC	breast:	n/a

No data

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

Extended variants
information (count: 593 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:593 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16934660	chr9:16432544-16432545	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs537269117	chr9:16432551-16432552	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs568132601	chr9:16432561-16432562	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs535687595	chr9:16432624-16432625	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs375479392	chr9:16432685-16432686	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs569573324	chr9:16432715-16432716	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs79416019	chr9:16432762-16432763	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs367745777	chr9:16432770-16432771	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs150567832	chr9:16432779-16432780	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs562546609	chr9:16432837-16432838	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs558480019	chr9:16432878-16432879	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs573202888	chr9:16432881-16432882	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs187722696	chr9:16432899-16432900	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs76479645	chr9:16432933-16432934	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs75720572	chr9:16433005-16433006	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs78406408	chr9:16433061-16433062	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs112265610	chr9:16433085-16433086	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs77566035	chr9:16433136-16433137	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs575087695	chr9:16433184-16433185	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs545741871	chr9:16433212-16433213	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs138576207	chr9:16433218-16433219	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs528108865	chr9:16433359-16433360	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs546541104	chr9:16433373-16433374	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs561654152	chr9:16433420-16433421	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs528936716	chr9:16433485-16433486	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs551204140	chr9:16433487-16433488	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs569511959	chr9:16433510-16433511	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs562118486	chr9:16433528-16433529	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs375284780	chr9:16433581-16433582	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs552130075	chr9:16433582-16433583	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs567135472	chr9:16433585-16433586	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs149333174	chr9:16433595-16433596	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs144606499	chr9:16433598-16433599	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs7871743	chr9:16433603-16433604	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs537991828	chr9:16433625-16433626	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs547626453	chr9:16433679-16433680	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs139717865	chr9:16433696-16433697	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs575126882	chr9:16433709-16433710	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs545578368	chr9:16433733-16433734	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs564239039	chr9:16433818-16433819	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs145039740	chr9:16433855-16433856	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs116435377	chr9:16433916-16433917	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs561683530	chr9:16433961-16433962	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs185142441	chr9:16433969-16433970	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs539768611	chr9:16433975-16433976	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs550741849	chr9:16433981-16433982	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs562547116	chr9:16434014-16434015	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs372758417	chr9:16434058-16434059	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs533597986	chr9:16434115-16434116	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs551914323	chr9:16434122-16434123	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

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
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
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:264 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:16416200-16435400	Weak transcription	Fetal Muscle Leg	muscle
2	chr9:16418000-16435600	Weak transcription	HUVEC	blood vessel
3	chr9:16418200-16435800	Weak transcription	Duodenum Smooth Muscle	Duodenum
4	chr9:16419400-16436200	Weak transcription	Fetal Muscle Trunk	muscle
5	chr9:16419600-16435200	Weak transcription	Fetal Intestine Large	intestine
6	chr9:16419600-16435400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr9:16419600-16435400	Weak transcription	Stomach Smooth Muscle	stomach
8	chr9:16419800-16432600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr9:16421800-16460400	Weak transcription	Aorta	Aorta
10	chr9:16422000-16435400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr9:16422800-16435400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr9:16426000-16442600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr9:16426200-16434200	Weak transcription	NHDF-Ad	bronchial
14	chr9:16426200-16434400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr9:16426200-16434400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr9:16426200-16435400	Weak transcription	Fetal Lung	lung
17	chr9:16426200-16435400	Weak transcription	Fetal Stomach	stomach
18	chr9:16426200-16435400	Weak transcription	HSMMtube	muscle
19	chr9:16426200-16436000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr9:16426200-16442600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr9:16426200-16445200	Weak transcription	Adipose Nuclei	Adipose
22	chr9:16426600-16435400	Weak transcription	Muscle Satellite Cultured Cells	--
23	chr9:16426600-16436000	Weak transcription	A549	lung
24	chr9:16427000-16433200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr9:16427000-16434400	Weak transcription	NHLF	lung
26	chr9:16427200-16434400	Weak transcription	NH-A	brain
27	chr9:16427400-16442600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr9:16427800-16433400	Weak transcription	HSMM	muscle
29	chr9:16428400-16441800	Weak transcription	Rectal Smooth Muscle	rectum
30	chr9:16428400-16442000	Weak transcription	Colon Smooth Muscle	Colon
31	chr9:16429600-16436600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr9:16430000-16434600	Weak transcription	Osteobl	bone
33	chr9:16430000-16435400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr9:16430200-16435200	Weak transcription	Ovary	ovary
35	chr9:16430600-16433200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr9:16430600-16434600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr9:16431400-16433800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr9:16431600-16432800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr9:16431800-16432800	Enhancers	H1 Cell Line	embryonic stem cell
40	chr9:16431800-16432800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr9:16431800-16432800	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr9:16431800-16433200	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr9:16432000-16432800	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr9:16432000-16433000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr9:16432000-16433200	Enhancers	iPS-20b Cell Line	embryonic stem cell
46	chr9:16432000-16433400	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr9:16432000-16435400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr9:16432200-16433200	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr9:16432400-16432600	Enhancers	H9 Cell Line	embryonic stem cell
50	chr9:16432400-16432800	Enhancers	iPS-15b Cell Line	embryonic stem cell

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