Variant report

Variant	nsv892614
Chromosome Location	chr9:14712257-14756969
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:183)
CpG islands
(count:245)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:183 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr9:14722642-14723053	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr9:14722568-14723014	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL11A	chr9:14722811-14722999	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr9:14751524-14751618	K562	blood:	n/a	n/a
5	CEBPB	chr9:14756265-14756314	HepG2	liver:	n/a	n/a
6	CEBPB	chr9:14720785-14721085	A549	lung:	n/a	chr9:14720966-14720983
7	CREB1	chr9:14741415-14741701	GM12878	blood:	n/a	n/a
8	CTCF	chr9:14714859-14714893	Fibrobl	skin:	n/a	n/a
9	CTCF	chr9:14739140-14739290	GM12878	blood:	n/a	n/a
10	CTCF	chr9:14742360-14742510	BE2_C	brain:	n/a	n/a
11	CTCF	chr9:14742160-14742310	BE2_C	brain:	n/a	n/a
12	CTCF	chr9:14742140-14742290	BE2_C	brain:	n/a	n/a
13	CTCF	chr9:14746280-14746430	GM12875	blood:	n/a	n/a
14	CTCF	chr9:14747313-14747353	Fibrobl	skin:	n/a	n/a
15	E2F4	chr9:14749811-14749898	MCF10A-Er-Src	breast:	n/a	n/a
16	EP300	chr9:14755936-14757233	SK-N-SH	brain:	n/a	chr9:14756319-14756333 chr9:14756115-14756125
17	EP300	chr9:14722544-14723149	H1-hESC	embryonic stem cell:	n/a	chr9:14722744-14722753 chr9:14722809-14722819
18	FOS	chr9:14747100-14747500	MCF10A-Er-Src	breast:	n/a	n/a
19	FOS	chr9:14750672-14751258	HUVEC	blood vessel:	n/a	n/a
20	FOS	chr9:14747156-14747453	MCF10A-Er-Src	breast:	n/a	n/a
21	FOS	chr9:14747099-14747500	MCF10A-Er-Src	breast:	n/a	n/a
22	FOS	chr9:14713528-14713631	MCF10A-Er-Src	breast:	n/a	n/a
23	FOS	chr9:14752149-14752609	HUVEC	blood vessel:	n/a	n/a
24	FOS	chr9:14747157-14747449	MCF10A-Er-Src	breast:	n/a	n/a
25	FOS	chr9:14746615-14747547	HUVEC	blood vessel:	n/a	chr9:14746832-14746839 chr9:14746829-14746840 chr9:14746831-14746839
26	FOSL2	chr9:14727977-14728315	HepG2	liver:	n/a	n/a
27	FOSL2	chr9:14731700-14732024	HepG2	liver:	n/a	n/a
28	FOSL2	chr9:14731055-14731610	HepG2	liver:	n/a	n/a
29	GATA2	chr9:14751815-14752654	HUVEC	blood vessel:	n/a	n/a
30	GATA2	chr9:14756175-14756494	SH-SY5Y	brain:	n/a	n/a
31	GATA2	chr9:14750842-14751154	HUVEC	blood vessel:	n/a	n/a
32	GATA2	chr9:14746171-14747513	HUVEC	blood vessel:	n/a	n/a
33	GATA3	chr9:14756113-14756487	MCF-7	breast:	n/a	n/a
34	GATA3	chr9:14752468-14752600	SH-SY5Y	brain:	n/a	n/a
35	GATA3	chr9:14756234-14756500	SH-SY5Y	brain:	n/a	n/a
36	GATA3	chr9:14756212-14756535	MCF-7	breast:	n/a	n/a
37	GTF2F1	chr9:14722869-14723065	H1-hESC	embryonic stem cell:	n/a	n/a
38	HDAC2	chr9:14722605-14723076	H1-hESC	embryonic stem cell:	n/a	n/a
39	JUN	chr9:14746650-14747436	HUVEC	blood vessel:	n/a	chr9:14746832-14746839 chr9:14746831-14746839
40	JUN	chr9:14722746-14723114	H1-hESC	embryonic stem cell:	n/a	n/a
41	JUND	chr9:14722698-14723115	H1-hESC	embryonic stem cell:	n/a	n/a
42	JUND	chr9:14722734-14723038	H1-hESC	embryonic stem cell:	n/a	n/a
43	MAFF	chr9:14733156-14733505	K562	blood:	n/a	chr9:14733322-14733340
44	MAFF	chr9:14748127-14748293	HepG2	liver:	n/a	chr9:14748177-14748195
45	MAFF	chr9:14733144-14733510	HepG2	liver:	n/a	chr9:14733322-14733340
46	MAFF	chr9:14737934-14738174	HepG2	liver:	n/a	n/a
47	MAFF	chr9:14713227-14713698	HepG2	liver:	n/a	n/a
48	MAFF	chr9:14713278-14713496	K562	blood:	n/a	n/a
49	MAFK	chr9:14713353-14713485	H1-hESC	embryonic stem cell:	n/a	n/a
50	MAFK	chr9:14745926-14746080	HepG2	liver:	n/a	chr9:14745988-14746004 chr9:14745995-14746005 chr9:14745989-14746009 chr9:14745993-14746002

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:14749903-14749953	GM06990	blood:	n/a
2	chr9:14749903-14749953	GM06990	blood:	n/a
3	chr9:14723496-14723546	HRPEpiC	eye:	n/a
4	chr9:14749903-14749953	NT2-D1	testis:	n/a
5	chr9:14723496-14723546	HCF	heart:	n/a
6	chr9:14723496-14723546	ProgFib	skin:	n/a
7	chr9:14722864-14722914	K562	blood:	n/a
8	chr9:14720244-14720294	HCT-116	colon:	n/a
9	chr9:14749903-14749953	HRCEpiC	kidney:	n/a
10	chr9:14722864-14722914	HEEpiC	esophagus:	n/a
11	chr9:14720244-14720294	PFSK-1	brain:	n/a
12	chr9:14722864-14722914	HCM	heart:	n/a
13	chr9:14720244-14720294	AG04449	skin:	fetal
14	chr9:14722864-14722914	BJ	skin:	n/a
15	chr9:14720244-14720294	HMEC	breast:	n/a
16	chr9:14722864-14722914	HPAEpiC	pulmonary alveolar:	n/a
17	chr9:14723496-14723546	ovcar-3	ovarian:	n/a
18	chr9:14722864-14722914	ovcar-3	ovarian:	n/a
19	chr9:14749903-14749953	NHDF-neo	bronchial:	n/a
20	chr9:14722864-14722914	HNPCEpiC	eye:	n/a
21	chr9:14720244-14720294	AG04450	lung:	fetal
22	chr9:14722864-14722914	NT2-D1	testis:	n/a
23	chr9:14723496-14723546	Caco-2	colon:	n/a
24	chr9:14749903-14749953	GM19239	blood:	n/a
25	chr9:14749903-14749953	HRE	kidney:	n/a
26	chr9:14749903-14749953	SK-N-MC	brain:	n/a
27	chr9:14723496-14723546	Hela-S3	cervix:	n/a
28	chr9:14749903-14749953	Hepatocyte	liver:	n/a
29	chr9:14749903-14749953	BJ	skin:	n/a
30	chr9:14723496-14723546	AG09309	skin:	n/a
31	chr9:14749903-14749953	HAEpiC	amniotic membrane:	n/a
32	chr9:14723496-14723546	K562	blood:	n/a
33	chr9:14723496-14723546	SKMC	muscle:	n/a
34	chr9:14722864-14722914	Caco-2	colon:	n/a
35	chr9:14720244-14720294	H1-hESC	embryonic stem cell:	embryo
36	chr9:14723496-14723546	NB4	blood:	n/a
37	chr9:14749903-14749953	SK-N-SH	brain:	n/a
38	chr9:14722864-14722914	GM12892	blood:	n/a
39	chr9:14749903-14749953	PrEC	prostate:	n/a
40	chr9:14749903-14749953	HCF	heart:	n/a
41	chr9:14722864-14722914	GM12878	blood:	n/a
42	chr9:14723496-14723546	GM06990	blood:	n/a
43	chr9:14720244-14720294	MCF10A-Er-Src	breast:	n/a
44	chr9:14749903-14749953	HL-60	blood:	n/a
45	chr9:14722864-14722914	MCF10A-Er-Src	breast:	n/a
46	chr9:14723496-14723546	HNPCEpiC	eye:	n/a
47	chr9:14720244-14720294	SK-N-SH_RA	brain:	n/a
48	chr9:14749903-14749953	GM12891	blood:	n/a
49	chr9:14749903-14749953	MCF-7	breast:	n/a
50	chr9:14749903-14749953	GM12878	blood:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:14692738..14695647-chr9:14753924..14755803,2	MCF-7	breast:
2	chr9:14693520..14695525-chr9:14717829..14719510,2	MCF-7	breast:
3	chr9:14677358..14679032-chr9:14729314..14731148,2	MCF-7	breast:
4	chr21:20745898..20746419-chr9:14747590..14748110,2	MCF-7	breast:
5	chr9:14692067..14693708-chr9:14756273..14757823,2	MCF-7	breast:
6	chr9:14690708..14693231-chr9:14713433..14715842,2	MCF-7	breast:
7	chr9:14723716..14725255-chr9:14725943..14728400,2	K562	blood:
8	chr9:14723716..14725255-chr9:14725943..14728400,2	K562	blood:
9	chr9:14692069..14694193-chr9:14751861..14753401,2	MCF-7	breast:
10	chr9:14691736..14693392-chr9:14716118..14717957,2	MCF-7	breast:
11	chr9:14406326..14406836-chr9:14756241..14756794,2	MCF-7	breast:

No data

Variant related genes	Relation type
CER1	TF binding region
CER1	CpG island
ENSG00000175893	chromatin interactions

Extended variants
information (count: 2122 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:2122 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7024505	chr9:14712257-14712258	Weak transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs142433111	chr9:14712309-14712310	Weak transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs531022577	chr9:14712330-14712331	Weak transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs116304119	chr9:14712336-14712337	Weak transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs79991369	chr9:14712365-14712366	Weak transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs192294671	chr9:14712367-14712368	Weak transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs371627272	chr9:14712399-14712400	Weak transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs184356423	chr9:14712440-14712441	Weak transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs1154781	chr9:14712456-14712457	Weak transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs114947576	chr9:14712495-14712496	Weak transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs569091094	chr9:14712571-14712572	Weak transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs537646598	chr9:14712591-14712592	Weak transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs189698282	chr9:14712597-14712598	Weak transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs556499472	chr9:14712616-14712617	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs567850324	chr9:14712636-14712637	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs116233634	chr9:14712672-14712673	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs151325713	chr9:14712676-14712677	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs576424616	chr9:14712689-14712690	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs181344699	chr9:14712722-14712723	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs558991689	chr9:14712776-14712777	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs10961678	chr9:14712806-14712807	Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs577904129	chr9:14712813-14712814	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs112303024	chr9:14712827-14712828	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs544492582	chr9:14712849-14712850	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs79780510	chr9:14712887-14712888	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs185986985	chr9:14712918-14712919	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs114450622	chr9:14712923-14712924	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs115090534	chr9:14712965-14712966	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs532558204	chr9:14712981-14712982	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs115712467	chr9:14713017-14713018	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs562656559	chr9:14713036-14713037	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs531620325	chr9:14713039-14713040	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs563904243	chr9:14713042-14713043	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs142078891	chr9:14713043-14713044	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs548112510	chr9:14713053-14713054	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs575164439	chr9:14713062-14713063	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs150398777	chr9:14713076-14713077	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs147700777	chr9:14713096-14713097	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs189302534	chr9:14713123-14713124	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs570167601	chr9:14713142-14713143	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs142402975	chr9:14713161-14713162	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs529504742	chr9:14713168-14713169	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs556087694	chr9:14713186-14713187	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs78060116	chr9:14713194-14713195	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs79868581	chr9:14713277-14713278	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs369029742	chr9:14713304-14713305	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs181893802	chr9:14713326-14713327	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs540789560	chr9:14713327-14713328	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs74870265	chr9:14713364-14713365	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs577240129	chr9:14713375-14713376	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

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
early-passage human iPS cells	21368824	CNVD
Glioblastoma multiforme	18628472	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	21811587	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD

Chromatin state (count:368 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:14694000-14719400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr9:14704800-14719400	Weak transcription	Right Atrium	heart
3	chr9:14709200-14712600	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr9:14710000-14715000	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr9:14710400-14713600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr9:14710600-14717400	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr9:14710800-14714000	Enhancers	NHEK	skin
8	chr9:14712000-14713000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr9:14712000-14713400	Weak transcription	HMEC	breast
10	chr9:14712600-14713600	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr9:14712600-14714200	Enhancers	Placenta	Placenta
12	chr9:14713000-14714000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr9:14713400-14714000	Bivalent Enhancer	Primary B cells from peripheral blood	blood
14	chr9:14713400-14714000	Enhancers	HMEC	breast
15	chr9:14713600-14715200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr9:14713600-14716800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr9:14714000-14714200	Enhancers	Primary B cells from peripheral blood	blood
18	chr9:14715000-14717600	Strong transcription	HUES64 Cell Line	embryonic stem cell
19	chr9:14715200-14715400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr9:14716000-14716200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr9:14716800-14722600	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr9:14717800-14746200	Weak transcription	Pancreas	Pancrea
23	chr9:14719400-14720200	Strong transcription	Right Atrium	heart
24	chr9:14719400-14723200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr9:14719800-14720000	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
26	chr9:14719800-14720000	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
27	chr9:14719800-14721000	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
28	chr9:14720000-14720200	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
29	chr9:14720200-14720800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
30	chr9:14720200-14722200	Weak transcription	Right Atrium	heart
31	chr9:14720200-14723000	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
32	chr9:14720800-14721400	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
33	chr9:14721000-14721400	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
34	chr9:14721400-14722000	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
35	chr9:14721400-14722200	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
36	chr9:14721600-14721800	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
37	chr9:14721600-14722800	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
38	chr9:14721800-14722000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
39	chr9:14721800-14723000	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
40	chr9:14722000-14722200	Bivalent Enhancer	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr9:14722000-14722200	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr9:14722000-14722200	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
43	chr9:14722000-14722200	Enhancers	Esophagus	oesophagus
44	chr9:14722000-14722400	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
45	chr9:14722000-14722400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
46	chr9:14722000-14722400	Flanking Bivalent TSS/Enh	H9 Cell Line	embryonic stem cell
47	chr9:14722000-14722600	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
48	chr9:14722000-14722600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr9:14722000-14722800	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
50	chr9:14722000-14722800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell

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