Variant report

Variant	nsv615228
Chromosome Location	chr9:116907448-116933449
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:116917556-116917812	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:116916117-116916350	HepG2	liver:	n/a	n/a
3	BACH1	chr9:116919190-116919252	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr9:116918832-116918950	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr9:116916262-116917825	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr9:116916169-116916429	HepG2	liver:	n/a	chr9:116916326-116916342
7	BHLHE40	chr9:116925776-116926107	HepG2	liver:	n/a	n/a
8	BHLHE40	chr9:116917582-116917706	K562	blood:	n/a	n/a
9	BHLHE40	chr9:116916072-116916459	HepG2	liver:	n/a	chr9:116916326-116916342
10	BHLHE40	chr9:116916046-116916890	HepG2	liver:	n/a	chr9:116916562-116916578 chr9:116916504-116916520 chr9:116916326-116916342
11	BHLHE40	chr9:116917652-116917813	GM12878	blood:	n/a	n/a
12	BRCA1	chr9:116917608-116917881	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr9:116916125-116916314	HepG2	liver:	n/a	n/a
14	CCNT2	chr9:116917603-116917846	K562	blood:	n/a	n/a
15	CEBPB	chr9:116918614-116918817	HepG2	liver:	n/a	n/a
16	CEBPB	chr9:116918582-116919517	IMR90	lung:	n/a	n/a
17	CEBPB	chr9:116917541-116917736	HepG2	liver:	n/a	n/a
18	CEBPB	chr9:116917574-116917748	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr9:116920204-116920447	IMR90	lung:	n/a	n/a
20	CEBPD	chr9:116916078-116916534	HepG2	liver:	n/a	n/a
21	CHD1	chr9:116917619-116917971	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD1	chr9:116917409-116920757	IMR90	lung:	n/a	n/a
23	CHD2	chr9:116917730-116917764	GM12878	blood:	n/a	n/a
24	CHD2	chr9:116916895-116917095	HepG2	liver:	n/a	n/a
25	CHD2	chr9:116917633-116917951	Hela-S3	cervix:	n/a	n/a
26	CHD2	chr9:116916123-116916384	HepG2	liver:	n/a	chr9:116916326-116916336
27	CHD2	chr9:116925741-116926067	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr9:116917641-116917827	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr9:116925792-116926044	HepG2	liver:	n/a	n/a
30	CREB1	chr9:116917536-116918110	A549	lung:	n/a	n/a
31	CTBP2	chr9:116917548-116918440	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTBP2	chr9:116915982-116917075	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTBP2	chr9:116918708-116919951	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr9:116917660-116917810	HPF	lung:	n/a	chr9:116917702-116917720 chr9:116917722-116917740 chr9:116917715-116917728 chr9:116917725-116917738 chr9:116917712-116917730 chr9:116917705-116917718
35	CTCF	chr9:116917542-116917878	GM12892	blood:	n/a	chr9:116917702-116917720 chr9:116917722-116917740 chr9:116917715-116917728 chr9:116917725-116917738 chr9:116917712-116917730 chr9:116917705-116917718
36	CTCF	chr9:116916080-116916230	HCFaa	heart:	n/a	chr9:116916166-116916179 chr9:116916164-116916182
37	CTCF	chr9:116916080-116916230	AG09309	skin:	n/a	chr9:116916166-116916179 chr9:116916164-116916182
38	CTCF	chr9:116916140-116916254	LNCaP	prostate:	n/a	chr9:116916166-116916179 chr9:116916164-116916182
39	CTCF	chr9:116917471-116917893	HepG2	liver:	n/a	chr9:116917702-116917720 chr9:116917722-116917740 chr9:116917715-116917728 chr9:116917725-116917738 chr9:116917712-116917730 chr9:116917705-116917718
40	CTCF	chr9:116917524-116917869	GM19238	blood:	n/a	chr9:116917702-116917720 chr9:116917722-116917740 chr9:116917715-116917728 chr9:116917725-116917738 chr9:116917712-116917730 chr9:116917705-116917718
41	CTCF	chr9:116916294-116916295	Kidney_OC	kidney:	n/a	n/a
42	CTCF	chr9:116917660-116917810	BE2_C	brain:	n/a	chr9:116917702-116917720 chr9:116917722-116917740 chr9:116917715-116917728 chr9:116917725-116917738 chr9:116917712-116917730 chr9:116917705-116917718
43	CTCF	chr9:116917551-116917886	NHEK	skin:	n/a	chr9:116917702-116917720 chr9:116917722-116917740 chr9:116917715-116917728 chr9:116917725-116917738 chr9:116917712-116917730 chr9:116917705-116917718
44	CTCF	chr9:116917640-116917790	HCPEpiC	choroid plexus:	n/a	chr9:116917702-116917720 chr9:116917722-116917740 chr9:116917715-116917728 chr9:116917725-116917738 chr9:116917712-116917730 chr9:116917705-116917718
45	CTCF	chr9:116919003-116919304	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr9:116916080-116916230	AoAF	blood vessel:	n/a	chr9:116916166-116916179 chr9:116916164-116916182
47	CTCF	chr9:116917571-116917853	GM13977	blood:	n/a	chr9:116917702-116917720 chr9:116917722-116917740 chr9:116917715-116917728 chr9:116917725-116917738 chr9:116917712-116917730 chr9:116917705-116917718
48	CTCF	chr9:116917660-116917810	GM12874	blood:	n/a	chr9:116917702-116917720 chr9:116917722-116917740 chr9:116917715-116917728 chr9:116917725-116917738 chr9:116917712-116917730 chr9:116917705-116917718
49	CTCF	chr9:116917680-116917830	HAc	cerebellar:	n/a	chr9:116917702-116917720 chr9:116917722-116917740 chr9:116917715-116917728 chr9:116917725-116917738 chr9:116917712-116917730 chr9:116917705-116917718
50	CTCF	chr9:116917680-116917830	NHDF-neo	bronchial:	n/a	chr9:116917702-116917720 chr9:116917722-116917740 chr9:116917715-116917728 chr9:116917725-116917738 chr9:116917712-116917730 chr9:116917705-116917718

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:116932436-116932486	HL-60	blood:	n/a
2	chr9:116918247-116918297	HCM	heart:	n/a
3	chr9:116918183-116918233	HL-60	blood:	n/a
4	chr9:116914074-116914124	HRPEpiC	eye:	n/a
5	chr9:116916031-116916081	HPAEpiC	pulmonary alveolar:	n/a
6	chr9:116932028-116932078	GM12892	blood:	n/a
7	chr9:116930367-116930417	K562	blood:	n/a
8	chr9:116916031-116916081	HUVEC	blood vessel:	n/a
9	chr9:116917393-116917443	HCM	heart:	n/a
10	chr9:116929797-116929847	T-47D	breast:	n/a
11	chr9:116918183-116918233	K562	blood:	n/a
12	chr9:116918477-116918527	Caco-2	colon:	n/a
13	chr9:116929797-116929847	HEK293	kidney:	embryo
14	chr9:116929797-116929847	GM12892	blood:	n/a
15	chr9:116932436-116932486	AG09319	gingival:	n/a
16	chr9:116929797-116929847	PFSK-1	brain:	n/a
17	chr9:116918247-116918297	AG09309	skin:	n/a
18	chr9:116930367-116930417	U87	brain:	n/a
19	chr9:116916031-116916081	AoSMC	blood vessel:	n/a
20	chr9:116918247-116918297	Jurkat	blood:	n/a
21	chr9:116932028-116932078	SAEC	small airway:	n/a
22	chr9:116930367-116930417	ovcar-3	ovarian:	n/a
23	chr9:116918183-116918233	AG09319	gingival:	n/a
24	chr9:116918247-116918297	SAEC	small airway:	n/a
25	chr9:116917393-116917443	SKMC	muscle:	n/a
26	chr9:116932028-116932078	AoSMC	blood vessel:	n/a
27	chr9:116932436-116932486	HEEpiC	esophagus:	n/a
28	chr9:116932028-116932078	LNCaP	prostate:	n/a
29	chr9:116918477-116918527	Hepatocyte	liver:	n/a
30	chr9:116932028-116932078	AG09319	gingival:	n/a
31	chr9:116918477-116918527	HRCEpiC	kidney:	n/a
32	chr9:116918247-116918297	GM12878	blood:	n/a
33	chr9:116930367-116930417	PANC-1	pancreas:	n/a
34	chr9:116930367-116930417	SK-N-MC	brain:	n/a
35	chr9:116932028-116932078	PANC-1	pancreas:	n/a
36	chr9:116929797-116929847	ProgFib	skin:	n/a
37	chr9:116916031-116916081	HCPEpiC	choroid plexus:	n/a
38	chr9:116918183-116918233	NT2-D1	testis:	n/a
39	chr9:116930367-116930417	BJ	skin:	n/a
40	chr9:116917393-116917443	MCF10A-Er-Src	breast:	n/a
41	chr9:116914074-116914124	HRE	kidney:	n/a
42	chr9:116918183-116918233	GM06990	blood:	n/a
43	chr9:116932436-116932486	SKMC	muscle:	n/a
44	chr9:116932436-116932486	HCT-116	colon:	n/a
45	chr9:116918477-116918527	HMEC	breast:	n/a
46	chr9:116917393-116917443	K562	blood:	n/a
47	chr9:116930367-116930417	BE2_C	brain:	n/a
48	chr9:116917393-116917443	HUVEC	blood vessel:	n/a
49	chr9:116929797-116929847	PrEC	prostate:	n/a
50	chr9:116932436-116932486	NB4	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:116922253..116925161-chr9:116948030..116950142,2	MCF-7	breast:
2	chr9:116909854..116913482-chr9:116913961..116916713,3	MCF-7	breast:
3	chr9:116909854..116913482-chr9:116913961..116916713,3	MCF-7	breast:
4	chr9:116846273..116847216-chr9:116922173..116922681,2	MCF-7	breast:
5	chr9:116901825..116904823-chr9:116906598..116910253,3	K562	blood:
6	chr9:116918924..116921858-chr9:116922744..116925296,3	K562	blood:
7	chr9:116918121..116920168-chr9:116937255..116940070,3	K562	blood:
8	chr9:116906533..116909775-chr9:116912915..116915543,3	MCF-7	breast:
9	chr9:116914824..116917398-chr9:116971543..116973662,2	MCF-7	breast:
10	chr9:116927426..116928989-chr9:116941833..116943417,2	K562	blood:
11	chr9:116869891..116870803-chr9:116915238..116916605,3	MCF-7	breast:
12	chr9:116870237..116871907-chr9:116924776..116927376,2	MCF-7	breast:
13	chr9:116918924..116921858-chr9:116922744..116925296,3	K562	blood:
14	chr9:116932183..116936074-chr9:116938591..116942808,3	K562	blood:
15	chr9:116906533..116909775-chr9:116912915..116915543,3	MCF-7	breast:
16	chr9:116903323..116904967-chr9:116908753..116911536,2	K562	blood:
17	chr9:116894422..116897805-chr9:116912339..116915406,3	MCF-7	breast:
18	chr9:116869949..116870838-chr9:116915614..116916621,9	MCF-7	breast:
19	chr9:116917422..116918284-chr9:117067805..117069207,4	K562	blood:
20	chr9:116915372..116918710-chr9:116920861..116924845,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KIF12-3	chr9:116929050-116929727	NONHSAT134369
2	lnc-KIF12-3	chr9:116921639-116921808	NONHSAT134369
3	lnc-KIF12-2	chr9:116908781-116909341	NONHSAT134368
4	lnc-KIF12-3	chr9:116924897-116924972	NONHSAT134369
5	lnc-KIF12-3	chr9:116929847-116930010	NONHSAT134369
6	lnc-KIF12-3	chr9:116928407-116928523	NONHSAT134369
7	lnc-KIF12-2	chr9:116914873-116914992	NONHSAT134368

Variant related genes	Relation type
COL27A1	TF binding region
COL27A1	CpG island
ENSG00000207726	chromatin interactions
ENSG00000196739	chromatin interactions

Extended variants
information (count: 1111 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:1111 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10817573	chr9:116907448-116907449	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs540607815	chr9:116907451-116907452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs12352644	chr9:116907553-116907554	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs535489384	chr9:116907572-116907573	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs181801042	chr9:116907585-116907586	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs543723197	chr9:116907593-116907594	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs563910446	chr9:116907602-116907603	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs185580993	chr9:116907615-116907616	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs543149087	chr9:116907655-116907656	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs565057398	chr9:116907656-116907657	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs577101361	chr9:116907821-116907822	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs544408674	chr9:116907926-116907927	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs559870591	chr9:116907990-116907991	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs528525333	chr9:116908057-116908058	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs551822798	chr9:116908058-116908059	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs565248260	chr9:116908064-116908065	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs533269308	chr9:116908129-116908130	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs535758004	chr9:116908136-116908137	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs141889203	chr9:116908137-116908138	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs569875973	chr9:116908150-116908151	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs535281115	chr9:116908160-116908161	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs13300086	chr9:116908173-116908174	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs138072533	chr9:116908192-116908193	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs376228415	chr9:116908197-116908198	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs534385660	chr9:116908217-116908218	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs190193741	chr9:116908226-116908227	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs548316026	chr9:116908233-116908234	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs577525949	chr9:116908235-116908236	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs537796662	chr9:116908248-116908249	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs557362315	chr9:116908267-116908268	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs181893074	chr9:116908277-116908278	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs542832660	chr9:116908295-116908296	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs149458862	chr9:116908315-116908316	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs186419567	chr9:116908362-116908363	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs143850963	chr9:116908398-116908399	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs2002284	chr9:116908453-116908454	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs74307796	chr9:116908459-116908460	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs530805012	chr9:116908470-116908471	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs527308867	chr9:116908473-116908474	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs142750044	chr9:116908521-116908522	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs188805931	chr9:116908597-116908598	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs529112060	chr9:116908600-116908601	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs375070886	chr9:116908619-116908620	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs565504073	chr9:116908640-116908641	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs534420800	chr9:116908659-116908660	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs34048470	chr9:116908677-116908678	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs551058008	chr9:116908740-116908741	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs140903544	chr9:116908762-116908763	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs536628466	chr9:116908769-116908770	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs557664573	chr9:116908842-116908843	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Oral squamous cell carcinoma	17134496	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
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
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
small cell lung cancer	20016488	CNVD
Cardiac fibroma	18329553	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
Lung cancer	19147751	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16272173	CNVD
Bladder cancer	21909424	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	21509527	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Cervical cancer	16585170	CNVD
Ependymoma	19289631	CNVD
Melanoma	17363583	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1308 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:116892800-116916000	Weak transcription	Gastric	stomach
2	chr9:116902600-116907800	Enhancers	Fetal Muscle Leg	muscle
3	chr9:116906200-116908200	Weak transcription	HepG2	liver
4	chr9:116906600-116910800	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr9:116907600-116908400	Bivalent Enhancer	Placenta	Placenta
6	chr9:116907800-116908000	Enhancers	Right Ventricle	heart
7	chr9:116907800-116908800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr9:116908000-116916000	Weak transcription	Right Ventricle	heart
9	chr9:116908200-116908800	Enhancers	HepG2	liver
10	chr9:116908400-116908600	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr9:116908600-116909400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr9:116908800-116910000	Weak transcription	HepG2	liver
13	chr9:116909400-116909600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr9:116909600-116915200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr9:116910000-116910200	Enhancers	HepG2	liver
16	chr9:116910200-116910600	Weak transcription	HepG2	liver
17	chr9:116910600-116912400	Enhancers	HepG2	liver
18	chr9:116910800-116911200	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
19	chr9:116911200-116911400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
20	chr9:116911400-116913400	Enhancers	Placenta	Placenta
21	chr9:116911800-116913600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr9:116912000-116912200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr9:116912000-116912400	Enhancers	Adipose Nuclei	Adipose
24	chr9:116912000-116912400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
25	chr9:116912200-116913000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr9:116912400-116913200	Weak transcription	HepG2	liver
27	chr9:116912800-116913400	Enhancers	Skeletal Muscle Male	skeletal muscle
28	chr9:116912800-116914200	Enhancers	Left Ventricle	heart
29	chr9:116913000-116914000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr9:116913000-116914400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr9:116913000-116914600	Enhancers	Cortex derived primary cultured neurospheres	brain
32	chr9:116913200-116914800	Enhancers	Spleen	Spleen
33	chr9:116913200-116915800	Enhancers	HepG2	liver
34	chr9:116913800-116914000	Bivalent Enhancer	Stomach Smooth Muscle	stomach
35	chr9:116913800-116914200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr9:116913800-116914400	Bivalent Enhancer	Fetal Muscle Leg	muscle
37	chr9:116913800-116914600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
38	chr9:116914000-116914200	Bivalent Enhancer	Primary mononuclear cells fromperipheralblood	Blood
39	chr9:116914000-116914600	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr9:116914000-116914600	Enhancers	Breast Myoepithelial Primary Cells	Breast
41	chr9:116914000-116914600	Bivalent Enhancer	Brain Anterior Caudate	brain
42	chr9:116914000-116916600	Enhancers	Liver	Liver
43	chr9:116914200-116916000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr9:116914200-116916000	Weak transcription	Left Ventricle	heart
45	chr9:116914400-116914600	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr9:116914600-116915000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr9:116914600-116915800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
48	chr9:116914600-116915800	Weak transcription	Cortex derived primary cultured neurospheres	brain
49	chr9:116914800-116915800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
50	chr9:116914800-116915800	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell

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