Variant report

Variant	nsv6482
Chromosome Location	chr9:14673695-14718568
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:481)
CpG islands
(count:488)
Chromatin interactive
region (count:18)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:481 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr9:14688075-14688638	GM12878	blood:	n/a	n/a
2	ATF2	chr9:14693237-14693620	GM12878	blood:	n/a	n/a
3	BACH1	chr9:14693258-14693548	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCLAF1	chr9:14693175-14693606	GM12878	blood:	n/a	n/a
5	BCLAF1	chr9:14693199-14693708	GM12878	blood:	n/a	n/a
6	BCLAF1	chr9:14688097-14688460	GM12878	blood:	n/a	chr9:14688341-14688350
7	BHLHE40	chr9:14692950-14693814	GM12878	blood:	n/a	chr9:14693117-14693133
8	BHLHE40	chr9:14689247-14689350	GM12878	blood:	n/a	n/a
9	BHLHE40	chr9:14688140-14688529	GM12878	blood:	n/a	n/a
10	CCNT2	chr9:14693300-14693572	K562	blood:	n/a	n/a
11	CEBPB	chr9:14687100-14687489	IMR90	lung:	n/a	n/a
12	CEBPB	chr9:14710917-14711211	IMR90	lung:	n/a	n/a
13	CHD1	chr9:14693269-14693945	GM12878	blood:	n/a	n/a
14	CHD1	chr9:14693268-14693369	H1-hESC	embryonic stem cell:	n/a	n/a
15	CHD1	chr9:14688156-14688623	GM12878	blood:	n/a	n/a
16	CHD2	chr9:14692865-14693793	GM12878	blood:	n/a	chr9:14693027-14693037
17	CHD2	chr9:14693310-14693896	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr9:14692666-14692698	HepG2	liver:	n/a	n/a
19	CREB1	chr9:14693141-14693720	HepG2	liver:	n/a	n/a
20	CREB1	chr9:14693169-14693584	A549	lung:	n/a	n/a
21	CTBP2	chr9:14693233-14693890	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr9:14693000-14693150	SK-N-SH_RA	brain:	n/a	n/a
23	CTCF	chr9:14693000-14693150	GM12868	blood:	n/a	n/a
24	CTCF	chr9:14693053-14693117	GM10266	blood:	n/a	n/a
25	CTCF	chr9:14693000-14693150	GM12874	blood:	n/a	n/a
26	CTCF	chr9:14693001-14693155	GM19240	blood:	n/a	n/a
27	CTCF	chr9:14692960-14693110	GM12865	blood:	n/a	n/a
28	CTCF	chr9:14693050-14693106	NHEK	skin:	n/a	n/a
29	CTCF	chr9:14692960-14693110	SAEC	small airway:	n/a	n/a
30	CTCF	chr9:14693052-14693101	A549	lung:	n/a	n/a
31	CTCF	chr9:14693036-14693097	LNCaP	prostate:	n/a	n/a
32	CTCF	chr9:14693039-14693127	MCF-7	breast:	n/a	n/a
33	CTCF	chr9:14692990-14693150	GM19239	blood:	n/a	n/a
34	CTCF	chr9:14692967-14693157	GM12891	blood:	n/a	n/a
35	CTCF	chr9:14693366-14693448	Lung_OC	lung:	n/a	n/a
36	CTCF	chr9:14692940-14693090	HEEpiC	esophagus:	n/a	n/a
37	CTCF	chr9:14693020-14693170	HMEC	breast:	n/a	n/a
38	CTCF	chr9:14708792-14708853	LNCaP	prostate:	n/a	n/a
39	CTCF	chr9:14692940-14693090	GM12874	blood:	n/a	n/a
40	CTCF	chr9:14693000-14693150	GM12871	blood:	n/a	n/a
41	CTCF	chr9:14692980-14693130	GM12865	blood:	n/a	n/a
42	CTCF	chr9:14714859-14714893	Fibrobl	skin:	n/a	n/a
43	CTCF	chr9:14693260-14693410	AG04449	skin:	n/a	n/a
44	CTCF	chr9:14693388-14693415	GM19239	blood:	n/a	n/a
45	CTCF	chr9:14688244-14688406	GM12878	blood:	n/a	n/a
46	CTCF	chr9:14692987-14693163	MCF-7	breast:	n/a	n/a
47	CTCF	chr9:14693010-14693120	LNCaP	prostate:	n/a	n/a
48	CTCF	chr9:14693250-14693305	GM12892	blood:	n/a	n/a
49	CTCF	chr9:14686713-14686754	LNCaP	prostate:	n/a	n/a
50	CTCF	chr9:14693056-14693102	HepG2	liver:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:14691289-14691339	HEEpiC	esophagus:	n/a
2	chr9:14693648-14693698	NH-A	brain:	n/a
3	chr9:14693888-14693938	NT2-D1	testis:	n/a
4	chr9:14693082-14693132	ProgFib	skin:	n/a
5	chr9:14693538-14693588	HPAEpiC	pulmonary alveolar:	n/a
6	chr9:14693888-14693938	HEK293	kidney:	embryo
7	chr9:14693082-14693132	MCF-7	breast:	n/a
8	chr9:14691289-14691339	NHBE	bronchial:	n/a
9	chr9:14693648-14693698	PANC-1	pancreas:	n/a
10	chr9:14693648-14693698	GM12878	blood:	n/a
11	chr9:14692931-14692981	NHDF-neo	bronchial:	n/a
12	chr9:14693538-14693588	HepG2	liver:	n/a
13	chr9:14691289-14691339	HUVEC	blood vessel:	n/a
14	chr9:14693504-14693554	AG09309	skin:	n/a
15	chr9:14691289-14691339	HIPEpiC	eye:	n/a
16	chr9:14692931-14692981	GM06990	blood:	n/a
17	chr9:14693648-14693698	NT2-D1	testis:	n/a
18	chr9:14693888-14693938	ProgFib	skin:	n/a
19	chr9:14691289-14691339	MCF10A-Er-Src	breast:	n/a
20	chr9:14693888-14693938	PrEC	prostate:	n/a
21	chr9:14693648-14693698	HL-60	blood:	n/a
22	chr9:14693648-14693698	ECC-1	luminal epithelium:	n/a
23	chr9:14693648-14693698	NB4	blood:	n/a
24	chr9:14691289-14691339	IMR90	lung:	fetal
25	chr9:14693504-14693554	HEK293	kidney:	embryo
26	chr9:14693504-14693554	A549	lung:	n/a
27	chr9:14691289-14691339	SK-N-SH	brain:	n/a
28	chr9:14693648-14693698	SK-N-SH	brain:	n/a
29	chr9:14690531-14690581	HEK293	kidney:	embryo
30	chr9:14693504-14693554	AG04449	skin:	fetal
31	chr9:14693504-14693554	SK-N-SH	brain:	n/a
32	chr9:14693888-14693938	HCT-116	colon:	n/a
33	chr9:14692931-14692981	A549	lung:	n/a
34	chr9:14693538-14693588	T-47D	breast:	n/a
35	chr9:14693888-14693938	AG10803	skin:	n/a
36	chr9:14691289-14691339	GM12892	blood:	n/a
37	chr9:14693888-14693938	GM06990	blood:	n/a
38	chr9:14690531-14690581	HPAEpiC	pulmonary alveolar:	n/a
39	chr9:14691289-14691339	HCT-116	colon:	n/a
40	chr9:14693888-14693938	SKMC	muscle:	n/a
41	chr9:14693538-14693588	LNCaP	prostate:	n/a
42	chr9:14693504-14693554	AG09319	gingival:	n/a
43	chr9:14693504-14693554	RPTEC	kidney:	n/a
44	chr9:14693888-14693938	A549	lung:	n/a
45	chr9:14691289-14691339	CMK	blood:	n/a
46	chr9:14691289-14691339	ovcar-3	ovarian:	n/a
47	chr9:14690531-14690581	HEEpiC	esophagus:	n/a
48	chr9:14693504-14693554	GM19239	blood:	n/a
49	chr9:14693648-14693698	SK-N-SH_RA	brain:	n/a
50	chr9:14693082-14693132	Caco-2	colon:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:14685829..14688724-chr9:14693473..14695940,2	K562	blood:
2	chr9:14693520..14695525-chr9:14717829..14719510,2	MCF-7	breast:
3	chr9:14678774..14681640-chr9:14758881..14761517,2	MCF-7	breast:
4	chr9:14700452..14703179-chr9:14705217..14707235,2	MCF-7	breast:
5	chr9:14693520..14695525-chr9:14717829..14719510,2	MCF-7	breast:
6	chr10:61799790..61802033-chr9:14680041..14681542,2	MCF-7	breast:
7	chr9:14673551..14675387-chr9:14691158..14693433,2	MCF-7	breast:
8	chr9:14690708..14693231-chr9:14713433..14715842,2	MCF-7	breast:
9	chr9:14686674..14691236-chr9:14691548..14694778,7	MCF-7	breast:
10	chr9:14671286..14673264-chr9:14676237..14678702,2	K562	blood:
11	chr9:14691736..14693392-chr9:14716118..14717957,2	MCF-7	breast:
12	chr9:14677358..14679032-chr9:14729314..14731148,2	MCF-7	breast:
13	chr9:14690708..14693231-chr9:14713433..14715842,2	MCF-7	breast:
14	chr9:14700452..14703179-chr9:14705217..14707235,2	MCF-7	breast:
15	chr9:14691643..14693414-chr9:14700745..14703153,2	K562	blood:
16	chr9:14692215..14694584-chr9:14703998..14706013,2	MCF-7	breast:
17	chr9:14685829..14688724-chr9:14693473..14695940,2	K562	blood:
18	chr9:14676498..14678344-chr9:14692478..14694843,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CER1-1	chr9:14693227-14693263	NONHSAT130254
2	lnc-CER1-1	chr9:14677364-14677470	NONHSAT130254
3	lnc-CER1-1	chr9:14683569-14683727	NONHSAT130254
4	lnc-CER1-1	chr9:14680031-14680160	NONHSAT130254
5	lnc-CER1-1	chr9:14690335-14690383	NONHSAT130254

No data

Variant related genes	Relation type
ZDHHC21	TF binding region
ZDHHC21	CpG island
ENSG00000175893	chromatin interactions

Extended variants
information (count: 2236 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:2236 , 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	rs150335626	chr9:14673730-14673731	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs12338477	chr9:14673744-14673745	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs537764905	chr9:14673765-14673766	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs554820014	chr9:14673791-14673792	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs181065148	chr9:14673839-14673840	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs533932448	chr9:14673840-14673841	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs185319405	chr9:14673847-14673848	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs10961651	chr9:14673853-14673854	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs149838604	chr9:14673906-14673907	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs190220135	chr9:14673926-14673927	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs556178211	chr9:14673949-14673950	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs112298456	chr9:14673964-14673965	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs373940708	chr9:14674020-14674021	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs565683071	chr9:14674058-14674059	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs544582550	chr9:14674106-14674107	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs373180944	chr9:14674133-14674134	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs376163915	chr9:14674154-14674155	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs200140489	chr9:14674158-14674159	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs375522483	chr9:14674199-14674200	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs549187484	chr9:14674218-14674219	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs540427235	chr9:14674220-14674221	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs139052749	chr9:14674292-14674293	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs368628792	chr9:14674346-14674347	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs371202417	chr9:14674355-14674356	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs560243224	chr9:14674419-14674420	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs532455929	chr9:14674428-14674429	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs552220841	chr9:14674432-14674433	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs112857758	chr9:14674455-14674456	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs113938048	chr9:14674509-14674510	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs569177392	chr9:14674537-14674538	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs566129854	chr9:14674560-14674561	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs372800282	chr9:14674571-14674572	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs10961652	chr9:14674574-14674575	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs568333415	chr9:14674581-14674582	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs201206991	chr9:14674726-14674727	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs534025655	chr9:14674730-14674731	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs553987304	chr9:14674738-14674739	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs113520481	chr9:14674749-14674750	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs116577368	chr9:14674754-14674755	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs539554924	chr9:14674780-14674781	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs78913240	chr9:14674797-14674798	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs182452707	chr9:14674952-14674953	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs558278276	chr9:14675008-14675009	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs541800412	chr9:14675013-14675014	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs555010392	chr9:14675028-14675029	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs80212938	chr9:14675100-14675101	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs186641097	chr9:14675108-14675109	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs191993830	chr9:14675141-14675142	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs532537302	chr9:14675204-14675205	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs146065753	chr9:14675217-14675218	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:95)

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
Pancreatic cancer	21811587	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Chordoma	21215367	CNVD

Chromatin state (count:878 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:14631000-14692400	Weak transcription	HSMMtube	muscle
2	chr9:14634400-14686600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr9:14634600-14692400	Weak transcription	Gastric	stomach
4	chr9:14634600-14692600	Weak transcription	Aorta	Aorta
5	chr9:14652000-14687000	Weak transcription	Primary monocytes fromperipheralblood	blood
6	chr9:14653800-14687200	Weak transcription	Left Ventricle	heart
7	chr9:14654200-14686200	Weak transcription	Fetal Brain Male	brain
8	chr9:14654200-14692600	Weak transcription	Pancreas	Pancrea
9	chr9:14655000-14686800	Weak transcription	Psoas Muscle	Psoas
10	chr9:14655200-14679000	Weak transcription	Rectal Mucosa Donor 29	rectum
11	chr9:14655200-14690600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr9:14655400-14681400	Weak transcription	Rectal Mucosa Donor 31	rectum
13	chr9:14655400-14681600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
14	chr9:14655400-14689200	Weak transcription	Rectal Smooth Muscle	rectum
15	chr9:14655400-14690600	Weak transcription	Brain Angular Gyrus	brain
16	chr9:14655400-14690600	Weak transcription	Fetal Kidney	kidney
17	chr9:14655400-14691000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
18	chr9:14655400-14691400	Weak transcription	A549	lung
19	chr9:14655400-14692200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
20	chr9:14655600-14680800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
21	chr9:14655600-14686200	Weak transcription	Brain Anterior Caudate	brain
22	chr9:14655600-14686600	Weak transcription	NHDF-Ad	bronchial
23	chr9:14655600-14688200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr9:14655600-14692200	Weak transcription	Fetal Lung	lung
25	chr9:14655800-14686200	Weak transcription	Primary T cells fromperipheralblood	blood
26	chr9:14655800-14686200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr9:14655800-14686800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
28	chr9:14655800-14686800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr9:14655800-14687200	Weak transcription	Adipose Nuclei	Adipose
30	chr9:14655800-14692200	Weak transcription	Brain Inferior Temporal Lobe	brain
31	chr9:14656000-14692400	Weak transcription	Colonic Mucosa	Colon
32	chr9:14656200-14692400	Weak transcription	Primary T cells from cord blood	blood
33	chr9:14657000-14692600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr9:14657200-14686600	Weak transcription	Primary T helper cells fromperipheralblood	blood
35	chr9:14657400-14686400	Weak transcription	Fetal Intestine Small	intestine
36	chr9:14658200-14677800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
37	chr9:14658400-14676800	Weak transcription	Liver	Liver
38	chr9:14658400-14685800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr9:14658600-14680800	Weak transcription	Duodenum Mucosa	Duodenum
40	chr9:14658600-14688800	Weak transcription	Skeletal Muscle Female	skeletal muscle
41	chr9:14659000-14686200	Weak transcription	HUES48 Cell Line	embryonic stem cell
42	chr9:14659200-14686000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr9:14659600-14685800	Weak transcription	Fetal Muscle Leg	muscle
44	chr9:14659600-14692400	Weak transcription	Colon Smooth Muscle	Colon
45	chr9:14660000-14675800	Weak transcription	Primary B cells from cord blood	blood
46	chr9:14660000-14681400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
47	chr9:14660000-14686600	Weak transcription	Fetal Stomach	stomach
48	chr9:14660200-14691000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
49	chr9:14663000-14686200	Weak transcription	Brain Hippocampus Middle	brain
50	chr9:14663200-14689400	Weak transcription	Brain Cingulate Gyrus	brain

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