Variant report

Variant	nsv613647
Chromosome Location	chr9:14852141-15016475
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:977)
CpG islands
(count:489)
Chromatin interactive
region (count:6)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:14960946-14962339	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:14913278-14913856	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:14925038-14925148	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:14967513-14968337	HepG2	liver:	n/a	n/a
5	ARID3A	chr9:14882074-14882476	HepG2	liver:	n/a	n/a
6	ARID3A	chr9:14899812-14900038	HepG2	liver:	n/a	n/a
7	ARID3A	chr9:14908366-14908878	HepG2	liver:	n/a	n/a
8	ARID3A	chr9:14893420-14893599	HepG2	liver:	n/a	n/a
9	ARID3A	chr9:14868526-14869963	HepG2	liver:	n/a	chr9:14869168-14869184 chr9:14869167-14869183
10	ARID3A	chr9:14888518-14888791	HepG2	liver:	n/a	n/a
11	ATF1	chr9:14992118-14992479	K562	blood:	n/a	n/a
12	ATF1	chr9:14926973-14927434	K562	blood:	n/a	n/a
13	ATF1	chr9:14993152-14993450	K562	blood:	n/a	n/a
14	BATF	chr9:14992095-14992275	GM12878	blood:	n/a	n/a
15	BCL3	chr9:14974056-14974338	GM12878	blood:	n/a	n/a
16	BHLHE40	chr9:14961666-14961683	K562	blood:	n/a	n/a
17	BHLHE40	chr9:14993063-14993414	K562	blood:	n/a	n/a
18	CBX3	chr9:14993086-14993431	K562	blood:	n/a	n/a
19	CCNT2	chr9:14926887-14927432	K562	blood:	n/a	n/a
20	CCNT2	chr9:14993093-14993468	K562	blood:	n/a	chr9:14993195-14993204
21	CEBPB	chr9:14992111-14992396	K562	blood:	n/a	n/a
22	CEBPB	chr9:14993420-14993444	K562	blood:	n/a	n/a
23	CEBPB	chr9:14974036-14974356	A549	lung:	n/a	chr9:14974218-14974229
24	CEBPB	chr9:14975880-14976085	HepG2	liver:	n/a	n/a
25	CEBPB	chr9:14924966-14925246	A549	lung:	n/a	chr9:14925029-14925040 chr9:14925086-14925097
26	CEBPB	chr9:14949391-14949419	K562	blood:	n/a	n/a
27	CEBPB	chr9:15010647-15010868	HepG2	liver:	n/a	chr9:15010746-15010757 chr9:15010745-15010758
28	CEBPB	chr9:14924936-14925115	K562	blood:	n/a	chr9:14925029-14925040 chr9:14925086-14925097
29	CEBPB	chr9:14978624-14978819	IMR90	lung:	n/a	chr9:14978687-14978698
30	CEBPB	chr9:14945585-14945795	HepG2	liver:	n/a	chr9:14945603-14945614
31	CEBPB	chr9:14978650-14978695	A549	lung:	n/a	n/a
32	CEBPB	chr9:14899804-14900187	HepG2	liver:	n/a	chr9:14899992-14900003
33	CEBPB	chr9:14884179-14884475	HepG2	liver:	n/a	n/a
34	CEBPB	chr9:14978581-14978815	HepG2	liver:	n/a	chr9:14978687-14978698
35	CEBPB	chr9:14924863-14925268	HepG2	liver:	n/a	chr9:14925029-14925040 chr9:14925086-14925097
36	CEBPB	chr9:14941573-14941825	HepG2	liver:	n/a	chr9:14941720-14941731 chr9:14941718-14941731 chr9:14941718-14941729 chr9:14941720-14941729
37	CEBPB	chr9:14924866-14925231	IMR90	lung:	n/a	chr9:14925029-14925040 chr9:14925086-14925097
38	CEBPB	chr9:14877121-14877303	HepG2	liver:	n/a	n/a
39	CEBPB	chr9:14899853-14900153	K562	blood:	n/a	chr9:14899992-14900003
40	CEBPB	chr9:14974108-14974375	HepG2	liver:	n/a	chr9:14974218-14974229
41	CEBPB	chr9:14899811-14900187	HepG2	liver:	n/a	chr9:14899992-14900003
42	CEBPB	chr9:14924869-14925229	Hela-S3	cervix:	n/a	chr9:14925029-14925040 chr9:14925086-14925097
43	CEBPB	chr9:14960939-14961821	HepG2	liver:	n/a	n/a
44	CEBPB	chr9:14899731-14900204	HepG2	liver:	n/a	chr9:14899992-14900003
45	CEBPB	chr9:14868569-14869669	HepG2	liver:	n/a	n/a
46	CEBPB	chr9:14899873-14900096	HepG2	liver:	n/a	chr9:14899992-14900003
47	CEBPB	chr9:14905488-14905648	HepG2	liver:	n/a	chr9:14905524-14905535
48	CEBPD	chr9:14899837-14900073	HepG2	liver:	n/a	n/a
49	CEBPD	chr9:14868715-14869298	HepG2	liver:	n/a	n/a
50	CEBPD	chr9:14869355-14869588	HepG2	liver:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:14910315-14910365	HRPEpiC	eye:	n/a
2	chr9:14910315-14910365	HRPEpiC	eye:	n/a
3	chr9:14910689-14910739	H1-hESC	embryonic stem cell:	embryo
4	chr9:14908132-14908182	GM06990	blood:	n/a
5	chr9:14908132-14908182	T-47D	breast:	n/a
6	chr9:14993584-14993634	BJ	skin:	n/a
7	chr9:14910689-14910739	HepG2	liver:	n/a
8	chr9:14993466-14993516	SK-N-SH_RA	brain:	n/a
9	chr9:14993466-14993516	GM12878	blood:	n/a
10	chr9:14993584-14993634	Caco-2	colon:	n/a
11	chr9:14910315-14910365	BE2_C	brain:	n/a
12	chr9:14993584-14993634	K562	blood:	n/a
13	chr9:14993466-14993516	ProgFib	skin:	n/a
14	chr9:14908132-14908182	GM12891	blood:	n/a
15	chr9:14993466-14993516	AG04449	skin:	fetal
16	chr9:14910689-14910739	AG09309	skin:	n/a
17	chr9:14883945-14883995	AG04450	lung:	fetal
18	chr9:14910689-14910739	SAEC	small airway:	n/a
19	chr9:14883945-14883995	HIPEpiC	eye:	n/a
20	chr9:14978400-14978450	HEEpiC	esophagus:	n/a
21	chr9:14910689-14910739	SK-N-SH_RA	brain:	n/a
22	chr9:14910315-14910365	HCPEpiC	choroid plexus:	n/a
23	chr9:14992172-14992222	CMK	blood:	n/a
24	chr9:14992172-14992222	HRCEpiC	kidney:	n/a
25	chr9:14910689-14910739	HMEC	breast:	n/a
26	chr9:14978400-14978450	HEK293	kidney:	embryo
27	chr9:14908132-14908182	PFSK-1	brain:	n/a
28	chr9:14908132-14908182	CMK	blood:	n/a
29	chr9:14910689-14910739	SKMC	muscle:	n/a
30	chr9:14883945-14883995	PANC-1	pancreas:	n/a
31	chr9:14992172-14992222	BJ	skin:	n/a
32	chr9:14910689-14910739	HRE	kidney:	n/a
33	chr9:14993466-14993516	HCM	heart:	n/a
34	chr9:14910689-14910739	GM12891	blood:	n/a
35	chr9:14910315-14910365	MCF10A-Er-Src	breast:	n/a
36	chr9:14992172-14992222	HCM	heart:	n/a
37	chr9:14978400-14978450	GM12892	blood:	n/a
38	chr9:14978400-14978450	ECC-1	luminal epithelium:	n/a
39	chr9:14993584-14993634	HNPCEpiC	eye:	n/a
40	chr9:14910315-14910365	MCF-7	breast:	n/a
41	chr9:14910315-14910365	HAEpiC	amniotic membrane:	n/a
42	chr9:14908132-14908182	HCT-116	colon:	n/a
43	chr9:14910689-14910739	HL-60	blood:	n/a
44	chr9:14978400-14978450	HRCEpiC	kidney:	n/a
45	chr9:14883945-14883995	NH-A	brain:	n/a
46	chr9:14993584-14993634	HCM	heart:	n/a
47	chr9:14992172-14992222	T-47D	breast:	n/a
48	chr9:14910315-14910365	PANC-1	pancreas:	n/a
49	chr9:14908132-14908182	ECC-1	luminal epithelium:	n/a
50	chr9:14910315-14910365	HepG2	liver:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr20:52274228..52274993-chr9:14900093..14900641,2	MCF-7	breast:
2	chr9:14897379..14899021-chr9:14903144..14904953,2	MCF-7	breast:
3	chr9:14897379..14899021-chr9:14903144..14904953,2	MCF-7	breast:
4	chr9:14914097..14915785-chr9:14923708..14925930,2	K562	blood:
5	chr9:14850312..14853276-chr9:14856165..14857741,2	MCF-7	breast:
6	chr9:14914097..14915785-chr9:14923708..14925930,2	K562	blood:

(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	chr9:14979298-14979338	l_3739_chr9:14977433-14983179_testes
3	lnc-FREM1-1	chr9:14983147-14983179	l_3739_chr9:14977433-14983179_testes
4	lnc-FREM1-1	chr9:14977891-14977954	l_3739_chr9:14977433-14983179_testes
5	lnc-FREM1-1	chr9:14977434-14977699	l_3739_chr9:14977433-14983179_testes

No data

Variant related genes	Relation type
LDHAP4	TF binding region
FREM1	TF binding region
ENSG00000215237	TF binding region
LDHAP4	CpG island
FREM1	CpG island
ENSG00000215237	CpG island
ENSG00000199814	chromatin interactions

Extended variants
information (count: 7871 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:7871 , 50 per page) page: 1 2 3 4 5 6 7 ... 158

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1874105	chr9:14852141-14852142	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs369921283	chr9:14852165-14852166	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs542450217	chr9:14852256-14852257	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs561186589	chr9:14852274-14852275	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs531486971	chr9:14852294-14852295	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs543713730	chr9:14852315-14852316	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs16932357	chr9:14852341-14852342	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs201169451	chr9:14852347-14852348	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs558636799	chr9:14852375-14852376	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs532551668	chr9:14852411-14852412	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs547870634	chr9:14852423-14852424	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs559877075	chr9:14852424-14852425	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs139245400	chr9:14852427-14852428	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs188346117	chr9:14852428-14852429	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs570266584	chr9:14852452-14852453	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs150016290	chr9:14852474-14852475	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs552474526	chr9:14852480-14852481	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs2779497	chr9:14852491-14852492	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs534306690	chr9:14852506-14852507	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs368723499	chr9:14852507-14852508	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs180800061	chr9:14852523-14852524	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs145231413	chr9:14852559-14852560	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs554183010	chr9:14852563-14852564	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs7044206	chr9:14852585-14852586	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs554430960	chr9:14852597-14852598	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs187597886	chr9:14852600-14852601	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs190309808	chr9:14852613-14852614	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs543302766	chr9:14852623-14852624	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs565185366	chr9:14852664-14852665	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs539855741	chr9:14852674-14852675	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs541434368	chr9:14852675-14852676	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs149089258	chr9:14852683-14852684	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs574654630	chr9:14852693-14852694	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs376289129	chr9:14852701-14852702	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs145912081	chr9:14852733-14852734	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs556176530	chr9:14852735-14852736	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs548679905	chr9:14852748-14852749	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs563704385	chr9:14852751-14852752	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs182073784	chr9:14852754-14852755	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs186608380	chr9:14852755-14852756	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs552413051	chr9:14852765-14852766	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs190288297	chr9:14852769-14852770	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs377638006	chr9:14852779-14852780	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs535034341	chr9:14852810-14852811	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs546968401	chr9:14852816-14852817	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs147851625	chr9:14852829-14852830	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs80000410	chr9:14852845-14852846	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs141491760	chr9:14852859-14852860	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs554650566	chr9:14852861-14852862	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs576112313	chr9:14852871-14852872	Strong transcription 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
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	21811587	CNVD

Chromatin state (count:1577 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:14779800-14853200	Weak transcription	Placenta	Placenta
2	chr9:14801800-14857200	Strong transcription	HepG2	liver
3	chr9:14807400-14868600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr9:14824000-14852800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr9:14833400-14860600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr9:14838600-14854000	Strong transcription	Fetal Kidney	kidney
7	chr9:14842200-14852400	Weak transcription	Brain Hippocampus Middle	brain
8	chr9:14843400-14868800	Weak transcription	Pancreas	Pancrea
9	chr9:14844400-14853000	Strong transcription	Fetal Muscle Leg	muscle
10	chr9:14848000-14853000	Strong transcription	Adipose Nuclei	Adipose
11	chr9:14848200-14852400	Strong transcription	Fetal Muscle Trunk	muscle
12	chr9:14848400-14852600	Strong transcription	Duodenum Mucosa	Duodenum
13	chr9:14849600-14869000	Weak transcription	Small Intestine	intestine
14	chr9:14850200-14853200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr9:14850200-14857000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr9:14850200-14859000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr9:14850200-14869000	Weak transcription	Fetal Brain Male	brain
18	chr9:14850600-14852600	Strong transcription	Fetal Lung	lung
19	chr9:14850600-14852800	Strong transcription	Fetal Stomach	stomach
20	chr9:14850800-14853200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr9:14850800-14853200	Strong transcription	Fetal Intestine Large	intestine
22	chr9:14851000-14852200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr9:14851600-14863800	Weak transcription	Colon Smooth Muscle	Colon
24	chr9:14851800-14857000	Weak transcription	Aorta	Aorta
25	chr9:14852200-14857200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr9:14852400-14853400	Weak transcription	Fetal Muscle Trunk	muscle
27	chr9:14852600-14853000	Weak transcription	Fetal Lung	lung
28	chr9:14852600-14858600	Weak transcription	Duodenum Mucosa	Duodenum
29	chr9:14852800-14857000	Weak transcription	Fetal Stomach	stomach
30	chr9:14853000-14853400	Enhancers	Fetal Lung	lung
31	chr9:14853000-14857000	Weak transcription	Fetal Muscle Leg	muscle
32	chr9:14853000-14857200	Weak transcription	Adipose Nuclei	Adipose
33	chr9:14853200-14853400	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
34	chr9:14853200-14857200	Weak transcription	Fetal Intestine Large	intestine
35	chr9:14853200-14868800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr9:14853400-14853800	Strong transcription	Fetal Muscle Trunk	muscle
37	chr9:14853400-14857000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
38	chr9:14853400-14857000	Weak transcription	Fetal Lung	lung
39	chr9:14853800-14857200	Weak transcription	Fetal Muscle Trunk	muscle
40	chr9:14854000-14856800	Weak transcription	Fetal Kidney	kidney
41	chr9:14856800-14859800	Strong transcription	Fetal Kidney	kidney
42	chr9:14857000-14857800	Strong transcription	Fetal Muscle Leg	muscle
43	chr9:14857000-14857800	Strong transcription	Fetal Stomach	stomach
44	chr9:14857000-14858000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr9:14857000-14858400	Strong transcription	Aorta	Aorta
46	chr9:14857000-14859600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
47	chr9:14857000-14860200	Strong transcription	Fetal Lung	lung
48	chr9:14857200-14857400	Genic enhancers	HepG2	liver
49	chr9:14857200-14858200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr9:14857200-14859400	Strong transcription	Adipose Nuclei	Adipose

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