Variant report

Variant	nsv1050499
Chromosome Location	chr9:71616954-71647969
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:489)
CpG islands
(count:428)
Chromatin interactive
region (count:29)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:489 , 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	ARID3A	chr9:71635426-71635919	K562	blood:	n/a	n/a
2	ARID3A	chr9:71631852-71631872	K562	blood:	n/a	n/a
3	ARID3A	chr9:71634748-71635103	K562	blood:	n/a	n/a
4	ARID3A	chr9:71642563-71642873	K562	blood:	n/a	n/a
5	ATF1	chr9:71642591-71642873	K562	blood:	n/a	n/a
6	ATF1	chr9:71635543-71635967	K562	blood:	n/a	n/a
7	ATF1	chr9:71634756-71635094	K562	blood:	n/a	n/a
8	BACH1	chr9:71634639-71634975	K562	blood:	n/a	n/a
9	BHLHE40	chr9:71634550-71635063	K562	blood:	n/a	n/a
10	BHLHE40	chr9:71631696-71631742	K562	blood:	n/a	n/a
11	BHLHE40	chr9:71633440-71634093	K562	blood:	n/a	n/a
12	CBX3	chr9:71634637-71635116	K562	blood:	n/a	n/a
13	CBX3	chr9:71634767-71635088	K562	blood:	n/a	n/a
14	CBX3	chr9:71644508-71644794	K562	blood:	n/a	n/a
15	CBX3	chr9:71644422-71644945	K562	blood:	n/a	n/a
16	CCNT2	chr9:71623403-71623461	K562	blood:	n/a	n/a
17	CCNT2	chr9:71634748-71635750	K562	blood:	n/a	n/a
18	CEBPB	chr9:71642532-71642963	K562	blood:	n/a	n/a
19	CEBPB	chr9:71642667-71642952	HepG2	liver:	n/a	n/a
20	CEBPB	chr9:71621213-71621255	HepG2	liver:	n/a	n/a
21	CEBPB	chr9:71642544-71642945	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr9:71642624-71642951	A549	lung:	n/a	n/a
23	CEBPB	chr9:71622329-71622529	HepG2	liver:	n/a	chr9:71622451-71622462
24	CEBPB	chr9:71622410-71622544	K562	blood:	n/a	chr9:71622451-71622462
25	CEBPB	chr9:71622344-71622530	IMR90	lung:	n/a	chr9:71622451-71622462
26	CEBPB	chr9:71642612-71642931	IMR90	lung:	n/a	n/a
27	CEBPB	chr9:71642524-71642960	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr9:71642518-71642970	K562	blood:	n/a	n/a
29	CEBPB	chr9:71642608-71642955	MCF-7	breast:	n/a	n/a
30	CEBPB	chr9:71634509-71635001	K562	blood:	n/a	n/a
31	CEBPB	chr9:71634690-71635114	K562	blood:	n/a	n/a
32	CEBPD	chr9:71634734-71635203	K562	blood:	n/a	n/a
33	CEBPD	chr9:71634663-71635222	K562	blood:	n/a	n/a
34	CHD1	chr9:71642698-71642879	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr9:71634776-71635089	K562	blood:	n/a	n/a
36	CTCF	chr9:71642478-71642933	GM12878	blood:	n/a	n/a
37	CTCF	chr9:71642680-71642830	RPTEC	kidney:	n/a	n/a
38	CTCF	chr9:71642628-71642857	A549	lung:	n/a	n/a
39	CTCF	chr9:71633748-71633899	GM12878	blood:	n/a	n/a
40	CTCF	chr9:71642640-71642790	HepG2	liver:	n/a	n/a
41	CTCF	chr9:71642660-71642810	HRPEpiC	eye:	n/a	n/a
42	CTCF	chr9:71627804-71627970	GM19240	blood:	n/a	n/a
43	CTCF	chr9:71642640-71642790	HFF-Myc	foreskin:	n/a	n/a
44	CTCF	chr9:71642588-71642841	ECC-1	luminal epithelium:	n/a	n/a
45	CTCF	chr9:71629112-71629136	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr9:71642620-71642770	GM12874	blood:	n/a	n/a
47	CTCF	chr9:71633740-71633890	GM12875	blood:	n/a	n/a
48	CTCF	chr9:71642454-71642997	MCF-7	breast:	n/a	n/a
49	CTCF	chr9:71642700-71642850	HVMF	connective:	n/a	n/a
50	CTCF	chr9:71642600-71642750	HFF-Myc	foreskin:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:71628906-71628956	AG09309	skin:	n/a
2	chr9:71628906-71628956	AG09309	skin:	n/a
3	chr9:71628906-71628956	ECC-1	luminal epithelium:	n/a
4	chr9:71628906-71628956	HCF	heart:	n/a
5	chr9:71627524-71627574	AG10803	skin:	n/a
6	chr9:71631514-71631564	NT2-D1	testis:	n/a
7	chr9:71627667-71627717	SK-N-MC	brain:	n/a
8	chr9:71629130-71629180	NHDF-neo	bronchial:	n/a
9	chr9:71628906-71628956	AG04449	skin:	fetal
10	chr9:71623401-71623451	HCM	heart:	n/a
11	chr9:71627667-71627717	HL-60	blood:	n/a
12	chr9:71627667-71627717	GM12878	blood:	n/a
13	chr9:71631514-71631564	HEK293	kidney:	embryo
14	chr9:71629130-71629180	AG04449	skin:	fetal
15	chr9:71631514-71631564	HMEC	breast:	n/a
16	chr9:71647192-71647242	BJ	skin:	n/a
17	chr9:71627667-71627717	HEK293	kidney:	embryo
18	chr9:71647192-71647242	AG04449	skin:	fetal
19	chr9:71628906-71628956	LNCaP	prostate:	n/a
20	chr9:71647192-71647242	HNPCEpiC	eye:	n/a
21	chr9:71647192-71647242	HEEpiC	esophagus:	n/a
22	chr9:71629130-71629180	Hepatocyte	liver:	n/a
23	chr9:71628906-71628956	HPAEpiC	pulmonary alveolar:	n/a
24	chr9:71631514-71631564	AoSMC	blood vessel:	n/a
25	chr9:71627667-71627717	RPTEC	kidney:	n/a
26	chr9:71627667-71627717	GM19239	blood:	n/a
27	chr9:71627667-71627717	ovcar-3	ovarian:	n/a
28	chr9:71631514-71631564	IMR90	lung:	fetal
29	chr9:71623401-71623451	SK-N-MC	brain:	n/a
30	chr9:71628906-71628956	MCF10A-Er-Src	breast:	n/a
31	chr9:71623401-71623451	HRCEpiC	kidney:	n/a
32	chr9:71627667-71627717	HCT-116	colon:	n/a
33	chr9:71623401-71623451	GM12891	blood:	n/a
34	chr9:71628906-71628956	T-47D	breast:	n/a
35	chr9:71647192-71647242	HCPEpiC	choroid plexus:	n/a
36	chr9:71647192-71647242	HUVEC	blood vessel:	n/a
37	chr9:71631514-71631564	HCF	heart:	n/a
38	chr9:71627667-71627717	SK-N-SH_RA	brain:	n/a
39	chr9:71647192-71647242	HIPEpiC	eye:	n/a
40	chr9:71623401-71623451	MCF10A-Er-Src	breast:	n/a
41	chr9:71647192-71647242	SKMC	muscle:	n/a
42	chr9:71627524-71627574	AG04450	lung:	fetal
43	chr9:71628906-71628956	NHDF-neo	bronchial:	n/a
44	chr9:71629130-71629180	HCT-116	colon:	n/a
45	chr9:71629130-71629180	HRPEpiC	eye:	n/a
46	chr9:71647192-71647242	PrEC	prostate:	n/a
47	chr9:71631514-71631564	RPTEC	kidney:	n/a
48	chr9:71623401-71623451	RPTEC	kidney:	n/a
49	chr9:71647192-71647242	RPTEC	kidney:	n/a
50	chr9:71629130-71629180	RPTEC	kidney:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:71642182..71645609-chr9:71649881..71653003,5	K562	blood:
2	chr9:71622551..71625318-chr9:71628981..71631159,4	K562	blood:
3	chr9:71639276..71640998-chr9:71649555..71652246,2	MCF-7	breast:
4	chr9:71619036..71621267-chr9:71649234..71651665,2	K562	blood:
5	chr9:71634014..71636921-chr9:71638059..71641027,2	K562	blood:
6	chr9:71642300..71643929-chr9:71644528..71647295,2	MCF-7	breast:
7	chr9:71640222..71642541-chr9:71649127..71652222,3	MCF-7	breast:
8	chr9:71634014..71636230-chr9:71638337..71641027,2	K562	blood:
9	chr9:71646520..71648758-chr9:71649618..71651156,2	MCF-7	breast:
10	chr9:71621939..71625091-chr9:71631557..71634181,3	K562	blood:
11	chr9:71642108..71644566-chr9:71646491..71648725,2	K562	blood:
12	chr9:71614613..71617089-chr9:71618925..71621633,2	K562	blood:
13	chr9:71634014..71636230-chr9:71638337..71641027,2	K562	blood:
14	chr9:71637586..71639711-chr9:71650641..71653127,2	K562	blood:
15	chr9:71621939..71625091-chr9:71631557..71634181,3	K562	blood:
16	chr9:71634711..71636591-chr9:71649540..71651584,2	MCF-7	breast:
17	chr9:71642300..71643929-chr9:71644528..71647295,2	MCF-7	breast:
18	chr9:71642108..71644566-chr9:71646491..71648725,2	K562	blood:
19	chr9:71459672..71460600-chr9:71642433..71642935,2	K562	blood:
20	chr9:71614613..71617089-chr9:71618925..71621633,2	K562	blood:
21	chr9:71199440..71199949-chr9:71642261..71643160,3	MCF-7	breast:
22	chr9:71628740..71631389-chr9:71634679..71636239,2	K562	blood:
23	chr9:71199108..71199619-chr9:71642191..71643182,2	K562	blood:
24	chr9:71644052..71646200-chr9:71649443..71653055,3	MCF-7	breast:
25	chr9:71612570..71616113-chr9:71618356..71621633,3	K562	blood:
26	chr9:71612099..71614210-chr9:71616099..71618792,2	MCF-7	breast:
27	chr9:71634014..71636921-chr9:71638059..71641027,2	K562	blood:
28	chr9:71627843..71630592-chr9:71632071..71633725,3	K562	blood:
29	chr9:71647332..71649670-chr9:71650617..71653266,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRKACG-4	chr9:71625289-71625403	ucscGeneNc_uc004ahk_2
2	lnc-PRKACG-4	chr9:71624143-71625000	ucscGeneNc_uc004ahk_2

No data

Variant related genes	Relation type
PRKACG	TF binding region
FXN	TF binding region
PRKACG	CpG island
FXN	CpG island
ENSG00000165060	chromatin interactions
ENSG00000165059	chromatin interactions

Extended variants
information (count: 1165 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:1165 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs574491579	chr9:71617021-71617022	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs115783183	chr9:71617024-71617025	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs146830365	chr9:71617059-71617060	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs575177753	chr9:71617065-71617066	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs1888333	chr9:71617087-71617088	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs78058129	chr9:71617135-71617136	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs572652638	chr9:71617169-71617170	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs182144369	chr9:71617170-71617171	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs186164839	chr9:71617171-71617172	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs140590875	chr9:71617184-71617185	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs1888332	chr9:71617211-71617212	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs1888331	chr9:71617227-71617228	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs531220681	chr9:71617233-71617234	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs188633531	chr9:71617239-71617240	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs1888330	chr9:71617269-71617270	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs115855435	chr9:71617272-71617273	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs374565848	chr9:71617275-71617276	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs113569859	chr9:71617276-71617277	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs150411064	chr9:71617384-71617385	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs180723125	chr9:71617438-71617439	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs556677496	chr9:71617489-71617490	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs368549756	chr9:71617545-71617546	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs74777216	chr9:71617547-71617548	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs545358104	chr9:71617555-71617556	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs539052219	chr9:71617651-71617652	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs138121645	chr9:71617766-71617767	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs185024413	chr9:71617768-71617769	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs149646008	chr9:71617793-71617794	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs555564675	chr9:71617822-71617823	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs574821524	chr9:71617826-71617827	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs542349093	chr9:71617830-71617831	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs189830260	chr9:71617831-71617832	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs530887889	chr9:71617874-71617875	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs183872199	chr9:71617928-71617929	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs564742189	chr9:71617973-71617974	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs545417560	chr9:71617996-71617997	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs4745490	chr9:71618098-71618099	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs187653331	chr9:71618123-71618124	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs568681470	chr9:71618220-71618221	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs528979386	chr9:71618234-71618235	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs143369765	chr9:71618235-71618236	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs568617861	chr9:71618236-71618237	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs539011327	chr9:71618243-71618244	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs10781329	chr9:71618245-71618246	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
45	rs139251696	chr9:71618256-71618257	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs369608800	chr9:71618264-71618265	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs191430225	chr9:71618268-71618269	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs199967445	chr9:71618344-71618345	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs57669897	chr9:71618382-71618383	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs386414979	chr9:71618383-71618384	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	17899364	CNVD
Mantle cell lymphoma	19029149	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	20729466	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Oral cancer	21386901	CNVD
Epilepsy	22083797	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Bipolar disorder	18458673	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:408 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:71594800-71628400	Weak transcription	Spleen	Spleen
2	chr9:71595200-71628000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr9:71595200-71631600	Weak transcription	Gastric	stomach
4	chr9:71595800-71626200	Weak transcription	Colonic Mucosa	Colon
5	chr9:71597200-71626000	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr9:71598800-71623200	Weak transcription	Pancreas	Pancrea
7	chr9:71598800-71644600	Weak transcription	Right Atrium	heart
8	chr9:71604200-71617800	Strong transcription	Fetal Intestine Large	intestine
9	chr9:71606800-71623000	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr9:71606800-71626800	Weak transcription	HepG2	liver
11	chr9:71607400-71630600	Weak transcription	Aorta	Aorta
12	chr9:71607600-71628000	Weak transcription	Lung	lung
13	chr9:71613000-71624600	Strong transcription	Fetal Intestine Small	intestine
14	chr9:71613600-71619200	Weak transcription	Rectal Smooth Muscle	rectum
15	chr9:71613600-71619600	Strong transcription	Duodenum Mucosa	Duodenum
16	chr9:71614000-71617600	Weak transcription	Placenta	Placenta
17	chr9:71614200-71619400	Weak transcription	Right Ventricle	heart
18	chr9:71614400-71618200	Weak transcription	Brain Anterior Caudate	brain
19	chr9:71614600-71617400	Strong transcription	Rectal Mucosa Donor 29	rectum
20	chr9:71614600-71619600	Weak transcription	Fetal Lung	lung
21	chr9:71614600-71621200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr9:71614600-71623000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr9:71614600-71625200	Weak transcription	Fetal Stomach	stomach
24	chr9:71614600-71625800	Weak transcription	Primary neutrophils fromperipheralblood	blood
25	chr9:71614600-71626800	Weak transcription	Primary hematopoietic stem cells	blood
26	chr9:71614600-71626800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr9:71614600-71627400	Weak transcription	Monocytes-CD14+_RO01746	blood
28	chr9:71614600-71630800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr9:71614800-71619600	Weak transcription	Fetal Kidney	kidney
30	chr9:71614800-71627400	Weak transcription	GM12878-XiMat	blood
31	chr9:71615000-71618200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
32	chr9:71615000-71618400	Weak transcription	Left Ventricle	heart
33	chr9:71615800-71621400	Weak transcription	Fetal Heart	heart
34	chr9:71616000-71620200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr9:71616400-71617400	Strong transcription	Primary B cells from peripheral blood	blood
36	chr9:71616600-71617400	Strong transcription	Primary B cells from cord blood	blood
37	chr9:71617400-71618200	Weak transcription	Primary B cells from peripheral blood	blood
38	chr9:71617400-71620800	Weak transcription	Rectal Mucosa Donor 29	rectum
39	chr9:71617400-71621400	Weak transcription	Primary B cells from cord blood	blood
40	chr9:71617800-71618200	Weak transcription	Fetal Intestine Large	intestine
41	chr9:71618000-71618200	Enhancers	Cortex derived primary cultured neurospheres	brain
42	chr9:71618200-71620000	Strong transcription	Primary B cells from peripheral blood	blood
43	chr9:71618200-71625000	Strong transcription	Fetal Intestine Large	intestine
44	chr9:71618400-71619600	Enhancers	Left Ventricle	heart
45	chr9:71619000-71631200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
46	chr9:71619200-71619600	Enhancers	Rectal Smooth Muscle	rectum
47	chr9:71619400-71620000	Enhancers	Right Ventricle	heart
48	chr9:71619600-71620000	Enhancers	Fetal Kidney	kidney
49	chr9:71619600-71620000	Enhancers	Fetal Lung	lung
50	chr9:71619600-71621200	Weak transcription	Duodenum Mucosa	Duodenum

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