Variant report

Variant	nsv892621
Chromosome Location	chr9:14928013-15043692
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:557)
CpG islands
(count:244)
Chromatin interactive
region (count:2)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:557 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:14967513-14968337	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:14960946-14962339	HepG2	liver:	n/a	n/a
3	ATF1	chr9:14993152-14993450	K562	blood:	n/a	n/a
4	ATF1	chr9:14992118-14992479	K562	blood:	n/a	n/a
5	BATF	chr9:14992095-14992275	GM12878	blood:	n/a	n/a
6	BCL3	chr9:14974056-14974338	GM12878	blood:	n/a	n/a
7	BHLHE40	chr9:14993063-14993414	K562	blood:	n/a	n/a
8	BHLHE40	chr9:14961666-14961683	K562	blood:	n/a	n/a
9	CBX3	chr9:14993086-14993431	K562	blood:	n/a	n/a
10	CCNT2	chr9:14993093-14993468	K562	blood:	n/a	chr9:14993195-14993204
11	CEBPB	chr9:14960939-14961821	HepG2	liver:	n/a	n/a
12	CEBPB	chr9:14974108-14974375	HepG2	liver:	n/a	chr9:14974218-14974229
13	CEBPB	chr9:14978650-14978695	A549	lung:	n/a	n/a
14	CEBPB	chr9:14941573-14941825	HepG2	liver:	n/a	chr9:14941720-14941731 chr9:14941718-14941731 chr9:14941718-14941729 chr9:14941720-14941729
15	CEBPB	chr9:14978624-14978819	IMR90	lung:	n/a	chr9:14978687-14978698
16	CEBPB	chr9:14945585-14945795	HepG2	liver:	n/a	chr9:14945603-14945614
17	CEBPB	chr9:14974036-14974356	A549	lung:	n/a	chr9:14974218-14974229
18	CEBPB	chr9:14949391-14949419	K562	blood:	n/a	n/a
19	CEBPB	chr9:14993420-14993444	K562	blood:	n/a	n/a
20	CEBPB	chr9:14978581-14978815	HepG2	liver:	n/a	chr9:14978687-14978698
21	CEBPB	chr9:14992111-14992396	K562	blood:	n/a	n/a
22	CEBPB	chr9:15010647-15010868	HepG2	liver:	n/a	chr9:15010746-15010757 chr9:15010745-15010758
23	CEBPB	chr9:14975880-14976085	HepG2	liver:	n/a	n/a
24	CHD2	chr9:14993152-14993465	K562	blood:	n/a	n/a
25	CHD2	chr9:14961345-14962017	HepG2	liver:	n/a	n/a
26	CHD2	chr9:14993084-14993550	H1-hESC	embryonic stem cell:	n/a	n/a
27	CREB1	chr9:14993066-14993633	H1-hESC	embryonic stem cell:	n/a	n/a
28	CREB1	chr9:14961190-14962077	HepG2	liver:	n/a	n/a
29	CREB1	chr9:14993016-14993607	H1-hESC	embryonic stem cell:	n/a	n/a
30	CREB1	chr9:14993147-14993530	A549	lung:	n/a	n/a
31	CTCF	chr9:14961350-14961409	Lung_OC	lung:	n/a	n/a
32	CTCF	chr9:14967502-14967791	K562	blood:	n/a	n/a
33	CTCF	chr9:14968079-14968215	HepG2	liver:	n/a	n/a
34	CTCF	chr9:14967569-14967724	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr9:14993221-14993248	K562	blood:	n/a	n/a
36	CTCF	chr9:14967996-14968238	HepG2	liver:	n/a	n/a
37	CTCF	chr9:15034677-15034700	GM13976	blood:	n/a	n/a
38	CTCF	chr9:14935900-14936050	HCM	heart:	n/a	n/a
39	CTCF	chr9:14967544-14967728	K562	blood:	n/a	n/a
40	CTCF	chr9:15041473-15041603	HepG2	liver:	n/a	chr9:15041557-15041578 chr9:15041562-15041580
41	CTCF	chr9:14949559-14949568	Kidney_OC	kidney:	n/a	n/a
42	CTCF	chr9:15018293-15018526	MCF-7	breast:	n/a	n/a
43	CTCF	chr9:15042046-15042166	GM12878	blood:	n/a	n/a
44	CTCF	chr9:15018316-15018514	MCF-7	breast:	n/a	n/a
45	CTCF	chr9:14982580-14982730	Caco-2	colon:	n/a	n/a
46	CTCF	chr9:15018300-15018450	Caco-2	colon:	n/a	n/a
47	CTCF	chr9:14961760-14961801	Pancreas_OC	pancreas:	n/a	n/a
48	CTCF	chr9:14967626-14967662	MCF-7	breast:	n/a	n/a
49	CTCF	chr9:14978175-14978237	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr9:14967612-14967704	MCF-7	breast:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:14992172-14992222	HUVEC	blood vessel:	n/a
2	chr9:14992172-14992222	PrEC	prostate:	n/a
3	chr9:14978400-14978450	SK-N-MC	brain:	n/a
4	chr9:14993584-14993634	BJ	skin:	n/a
5	chr9:14992172-14992222	AG04449	skin:	fetal
6	chr9:14993466-14993516	NHDF-neo	bronchial:	n/a
7	chr9:14992172-14992222	MCF-7	breast:	n/a
8	chr9:14978400-14978450	SKMC	muscle:	n/a
9	chr9:14993466-14993516	AG09309	skin:	n/a
10	chr9:14978400-14978450	HPAEpiC	pulmonary alveolar:	n/a
11	chr9:14978400-14978450	HRPEpiC	eye:	n/a
12	chr9:14992172-14992222	NH-A	brain:	n/a
13	chr9:14993584-14993634	PANC-1	pancreas:	n/a
14	chr9:14978400-14978450	HRE	kidney:	n/a
15	chr9:14993466-14993516	GM12892	blood:	n/a
16	chr9:14993466-14993516	NHBE	bronchial:	n/a
17	chr9:14992172-14992222	AoSMC	blood vessel:	n/a
18	chr9:14993584-14993634	ovcar-3	ovarian:	n/a
19	chr9:14978400-14978450	ovcar-3	ovarian:	n/a
20	chr9:14992172-14992222	A549	lung:	n/a
21	chr9:14978400-14978450	HNPCEpiC	eye:	n/a
22	chr9:14992172-14992222	NB4	blood:	n/a
23	chr9:14993584-14993634	HRPEpiC	eye:	n/a
24	chr9:14993584-14993634	HRE	kidney:	n/a
25	chr9:14993466-14993516	Caco-2	colon:	n/a
26	chr9:14993466-14993516	Hepatocyte	liver:	n/a
27	chr9:14978400-14978450	A549	lung:	n/a
28	chr9:14993466-14993516	T-47D	breast:	n/a
29	chr9:14978400-14978450	HepG2	liver:	n/a
30	chr9:14992172-14992222	Hela-S3	cervix:	n/a
31	chr9:14992172-14992222	HepG2	liver:	n/a
32	chr9:14978400-14978450	RPTEC	kidney:	n/a
33	chr9:14978400-14978450	NH-A	brain:	n/a
34	chr9:14978400-14978450	NHDF-neo	bronchial:	n/a
35	chr9:14993466-14993516	HCF	heart:	n/a
36	chr9:14993584-14993634	MCF-7	breast:	n/a
37	chr9:14993466-14993516	SK-N-MC	brain:	n/a
38	chr9:14978400-14978450	MCF10A-Er-Src	breast:	n/a
39	chr9:14978400-14978450	HUVEC	blood vessel:	n/a
40	chr9:14993466-14993516	GM06990	blood:	n/a
41	chr9:14993584-14993634	GM12892	blood:	n/a
42	chr9:14992172-14992222	HCF	heart:	n/a
43	chr9:14993466-14993516	SKMC	muscle:	n/a
44	chr9:14978400-14978450	AG09309	skin:	n/a
45	chr9:14993466-14993516	HL-60	blood:	n/a
46	chr9:14978400-14978450	AoSMC	blood vessel:	n/a
47	chr9:14992172-14992222	CMK	blood:	n/a
48	chr9:14993584-14993634	GM19239	blood:	n/a
49	chr9:14993584-14993634	ECC-1	luminal epithelium:	n/a
50	chr9:14993466-14993516	HUVEC	blood vessel:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:15036109..15038088-chr9:15043149..15044736,2	MCF-7	breast:
2	chr9:15036109..15038088-chr9:15043149..15044736,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FREM1-1	chr9:14980226-14980343	l_3739_chr9:14977433-14983179_testes
2	lnc-FREM1-1	chr9:14977434-14977699	l_3739_chr9:14977433-14983179_testes
3	lnc-FREM1-1	chr9:14977891-14977954	l_3739_chr9:14977433-14983179_testes
4	lnc-FREM1-1	chr9:14979298-14979338	l_3739_chr9:14977433-14983179_testes
5	lnc-FREM1-1	chr9:14983147-14983179	l_3739_chr9:14977433-14983179_testes

No data

Variant related genes	Relation type
ENSG00000215237	TF binding region
ENSG00000215237	CpG island

Extended variants
information (count: 4439 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:4439 , 50 per page) page: 1 2 3 4 5 6 7 ... 89

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10511602	chr9:14928013-14928014	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs530382211	chr9:14928028-14928029	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs548620876	chr9:14928041-14928042	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs570354460	chr9:14928112-14928113	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs374460257	chr9:14928114-14928115	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs549854820	chr9:14928151-14928152	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs569501532	chr9:14928171-14928172	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs549409552	chr9:14928172-14928173	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs184899622	chr9:14928187-14928188	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs10738382	chr9:14928191-14928192	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs145309910	chr9:14928200-14928201	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs565753127	chr9:14928209-14928210	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs536520301	chr9:14928223-14928224	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs150576795	chr9:14928326-14928327	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs111998677	chr9:14928367-14928368	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs7865084	chr9:14928397-14928398	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs149677169	chr9:14928425-14928426	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs566021652	chr9:14928426-14928427	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs189744189	chr9:14928467-14928468	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs78898922	chr9:14928527-14928528	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs150614395	chr9:14928555-14928556	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs145459544	chr9:14928570-14928571	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs10756627	chr9:14928594-14928595	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs563820110	chr9:14928598-14928599	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs77455872	chr9:14928603-14928604	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs140303745	chr9:14928612-14928613	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs570920759	chr9:14928709-14928710	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs369159800	chr9:14928744-14928745	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs144033702	chr9:14928794-14928795	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs547112516	chr9:14928819-14928820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs565796759	chr9:14928927-14928928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs554375205	chr9:14928930-14928931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs536047619	chr9:14929011-14929012	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs386732956	chr9:14929020-14929021	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs115376713	chr9:14929021-14929022	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs76472721	chr9:14929027-14929028	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs558958129	chr9:14929076-14929077	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs545931472	chr9:14929109-14929110	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs377638454	chr9:14929124-14929125	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs114500370	chr9:14929137-14929138	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs75338695	chr9:14929141-14929142	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs146852115	chr9:14929187-14929188	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs113189612	chr9:14929208-14929209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs563910445	chr9:14929209-14929210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs180937948	chr9:14929225-14929226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs117433085	chr9:14929247-14929248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs185929933	chr9:14929275-14929276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs35794566	chr9:14929279-14929280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs561625998	chr9:14929307-14929308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs189151655	chr9:14929308-14929309	Weak transcription	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
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
Breast cancer	21611746	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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	21811587	CNVD
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:669 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:14920600-14935200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr9:14925200-14945400	Weak transcription	Aorta	Aorta
3	chr9:14925600-14928600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr9:14926000-14928800	Enhancers	Fetal Heart	heart
5	chr9:14926200-14928800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr9:14927200-14935200	Weak transcription	Fetal Stomach	stomach
7	chr9:14927400-14928200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr9:14927400-14932800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr9:14927400-14935400	Weak transcription	Fetal Kidney	kidney
10	chr9:14927600-14932000	Weak transcription	Primary hematopoietic stem cells	blood
11	chr9:14927600-14937000	Weak transcription	Fetal Lung	lung
12	chr9:14927800-14932000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
13	chr9:14928200-14932000	Weak transcription	Fetal Muscle Leg	muscle
14	chr9:14928800-14931000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr9:14929000-14929200	Enhancers	HepG2	liver
16	chr9:14931000-14931200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr9:14931200-14932200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr9:14932000-14932200	Enhancers	Primary hematopoietic stem cells	blood
19	chr9:14932000-14932400	Enhancers	Fetal Muscle Trunk	muscle
20	chr9:14932000-14932400	Enhancers	NHDF-Ad	bronchial
21	chr9:14932000-14932600	Enhancers	Fetal Muscle Leg	muscle
22	chr9:14932600-14933000	Weak transcription	Fetal Muscle Leg	muscle
23	chr9:14932800-14933000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr9:14932800-14933000	Enhancers	Fetal Brain Male	brain
25	chr9:14932800-14933200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr9:14933000-14933200	Enhancers	Fetal Muscle Leg	muscle
27	chr9:14933000-14941800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr9:14933200-14957200	Weak transcription	Fetal Muscle Leg	muscle
29	chr9:14934600-14935800	Enhancers	Fetal Brain Male	brain
30	chr9:14934600-14937400	Enhancers	Cortex derived primary cultured neurospheres	brain
31	chr9:14934600-14938200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr9:14935000-14937600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr9:14935200-14935600	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr9:14935200-14935600	Enhancers	Adipose Nuclei	Adipose
35	chr9:14935200-14936000	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr9:14935200-14937000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr9:14935200-14937200	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr9:14935200-14937200	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr9:14935200-14937200	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr9:14935200-14937400	Enhancers	Colon Smooth Muscle	Colon
41	chr9:14935200-14937600	Enhancers	Fetal Stomach	stomach
42	chr9:14935200-14939200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr9:14935400-14935800	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr9:14935400-14935800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr9:14935400-14936600	Enhancers	Fetal Kidney	kidney
46	chr9:14935400-14937400	Enhancers	Fetal Brain Female	brain
47	chr9:14935600-14936600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr9:14935800-14936200	Weak transcription	Fetal Brain Male	brain
49	chr9:14935800-14937000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
50	chr9:14935800-14938800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links