Variant report

Variant	nsv466524
Chromosome Location	chr9:116826842-116867054
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1086)
CpG islands
(count:855)
Chromatin interactive
region (count:43)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1086 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:116844279-116845083	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:116842638-116844032	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:116840488-116840966	HepG2	liver:	n/a	n/a
4	ATF3	chr9:116842974-116843531	A549	lung:	n/a	n/a
5	ATF3	chr9:116842433-116843590	A549	lung:	n/a	n/a
6	BACH1	chr9:116840541-116841228	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr9:116840658-116841126	K562	blood:	n/a	n/a
8	BCL3	chr9:116842282-116843923	A549	lung:	n/a	chr9:116843045-116843054 chr9:116843046-116843055
9	BCL3	chr9:116842806-116843812	A549	lung:	n/a	chr9:116843045-116843054 chr9:116843046-116843055
10	BCL3	chr9:116844297-116845192	A549	lung:	n/a	n/a
11	BHLHE40	chr9:116838098-116838321	HepG2	liver:	n/a	n/a
12	BHLHE40	chr9:116844832-116845056	GM12878	blood:	n/a	n/a
13	BHLHE40	chr9:116844108-116845133	HepG2	liver:	n/a	n/a
14	BHLHE40	chr9:116840430-116841326	HepG2	liver:	n/a	n/a
15	BRCA1	chr9:116840522-116840580	HepG2	liver:	n/a	chr9:116840536-116840543
16	BRCA1	chr9:116844351-116845068	HepG2	liver:	n/a	n/a
17	BRCA1	chr9:116843080-116843583	HepG2	liver:	n/a	n/a
18	CBX3	chr9:116864751-116865191	HCT-116	colon:	n/a	n/a
19	CBX3	chr9:116844650-116845093	K562	blood:	n/a	n/a
20	CBX3	chr9:116864807-116865125	K562	blood:	n/a	n/a
21	CBX3	chr9:116864794-116865133	K562	blood:	n/a	n/a
22	CEBPB	chr9:116844347-116845055	HepG2	liver:	n/a	chr9:116844531-116844544 chr9:116844533-116844544
23	CEBPB	chr9:116843085-116843653	A549	lung:	n/a	n/a
24	CEBPB	chr9:116844432-116844633	HepG2	liver:	n/a	chr9:116844531-116844544 chr9:116844533-116844544
25	CEBPB	chr9:116832616-116832630	HepG2	liver:	n/a	n/a
26	CEBPB	chr9:116844846-116845109	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr9:116843161-116843532	HepG2	liver:	n/a	n/a
28	CEBPB	chr9:116842549-116843727	A549	lung:	n/a	n/a
29	CEBPB	chr9:116843102-116843647	HepG2	liver:	n/a	n/a
30	CEBPB	chr9:116844434-116845166	A549	lung:	n/a	chr9:116844531-116844544 chr9:116844533-116844544
31	CEBPB	chr9:116840525-116840881	HepG2	liver:	n/a	n/a
32	CEBPB	chr9:116843108-116843979	HepG2	liver:	n/a	chr9:116843795-116843806
33	CEBPB	chr9:116840439-116840891	HepG2	liver:	n/a	n/a
34	CEBPB	chr9:116831179-116831303	H1-hESC	embryonic stem cell:	n/a	chr9:116831285-116831298
35	CEBPB	chr9:116844308-116844769	HepG2	liver:	n/a	chr9:116844531-116844544 chr9:116844533-116844544
36	CEBPB	chr9:116843160-116843568	A549	lung:	n/a	n/a
37	CEBPB	chr9:116831154-116831332	IMR90	lung:	n/a	chr9:116831285-116831298 chr9:116831307-116831319
38	CEBPB	chr9:116844213-116845089	HepG2	liver:	n/a	chr9:116844531-116844544 chr9:116844533-116844544
39	CEBPB	chr9:116844795-116845110	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr9:116831120-116831410	HepG2	liver:	n/a	chr9:116831285-116831298 chr9:116831307-116831319
41	CEBPD	chr9:116840273-116840979	HepG2	liver:	n/a	n/a
42	CEBPD	chr9:116843056-116843916	HepG2	liver:	n/a	n/a
43	CEBPD	chr9:116843971-116844736	HepG2	liver:	n/a	n/a
44	CEBPD	chr9:116844286-116844673	HepG2	liver:	n/a	n/a
45	CEBPD	chr9:116843251-116843649	HepG2	liver:	n/a	n/a
46	CEBPZ	chr9:116828479-116828533	HepG2	liver:	n/a	n/a
47	CHD1	chr9:116861095-116861396	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr9:116840394-116840956	HepG2	liver:	n/a	n/a
49	CHD2	chr9:116842857-116843975	HepG2	liver:	n/a	n/a
50	CHD2	chr9:116844277-116845112	HepG2	liver:	n/a	n/a

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:116860500-116860550	SK-N-MC	brain:	n/a
2	chr9:116860500-116860550	SK-N-MC	brain:	n/a
3	chr9:116861532-116861582	SK-N-SH_RA	brain:	n/a
4	chr9:116861288-116861338	NHDF-neo	bronchial:	n/a
5	chr9:116861532-116861582	AG10803	skin:	n/a
6	chr9:116840435-116840485	ovcar-3	ovarian:	n/a
7	chr9:116861532-116861582	AG04450	lung:	fetal
8	chr9:116859631-116859681	U87	brain:	n/a
9	chr9:116860500-116860550	GM12878	blood:	n/a
10	chr9:116861442-116861492	HCT-116	colon:	n/a
11	chr9:116861288-116861338	HUVEC	blood vessel:	n/a
12	chr9:116861404-116861454	GM06990	blood:	n/a
13	chr9:116840825-116840875	ECC-1	luminal epithelium:	n/a
14	chr9:116861288-116861338	HPAEpiC	pulmonary alveolar:	n/a
15	chr9:116856710-116856760	Caco-2	colon:	n/a
16	chr9:116861288-116861338	HCF	heart:	n/a
17	chr9:116841084-116841134	T-47D	breast:	n/a
18	chr9:116860500-116860550	CMK	blood:	n/a
19	chr9:116840435-116840485	U87	brain:	n/a
20	chr9:116856710-116856760	HCT-116	colon:	n/a
21	chr9:116859631-116859681	PANC-1	pancreas:	n/a
22	chr9:116856710-116856760	MCF-7	breast:	n/a
23	chr9:116861442-116861492	NT2-D1	testis:	n/a
24	chr9:116861532-116861582	SK-N-MC	brain:	n/a
25	chr9:116840435-116840485	NHBE	bronchial:	n/a
26	chr9:116856710-116856760	HAEpiC	amniotic membrane:	n/a
27	chr9:116861404-116861454	HIPEpiC	eye:	n/a
28	chr9:116860500-116860550	Hela-S3	cervix:	n/a
29	chr9:116837795-116837845	AG09309	skin:	n/a
30	chr9:116841084-116841134	GM12891	blood:	n/a
31	chr9:116861404-116861454	HepG2	liver:	n/a
32	chr9:116861288-116861338	HCT-116	colon:	n/a
33	chr9:116860500-116860550	ProgFib	skin:	n/a
34	chr9:116861404-116861454	MCF10A-Er-Src	breast:	n/a
35	chr9:116856710-116856760	H1-hESC	embryonic stem cell:	embryo
36	chr9:116861288-116861338	K562	blood:	n/a
37	chr9:116837795-116837845	HUVEC	blood vessel:	n/a
38	chr9:116859631-116859681	GM19239	blood:	n/a
39	chr9:116856710-116856760	NHDF-neo	bronchial:	n/a
40	chr9:116837795-116837845	HEK293	kidney:	embryo
41	chr9:116860650-116860700	AG10803	skin:	n/a
42	chr9:116860437-116860487	Hela-S3	cervix:	n/a
43	chr9:116840435-116840485	HEEpiC	esophagus:	n/a
44	chr9:116861288-116861338	HIPEpiC	eye:	n/a
45	chr9:116841084-116841134	AG04449	skin:	fetal
46	chr9:116861442-116861492	BJ	skin:	n/a
47	chr9:116840825-116840875	HUVEC	blood vessel:	n/a
48	chr9:116841084-116841134	U87	brain:	n/a
49	chr9:116861404-116861454	PANC-1	pancreas:	n/a
50	chr9:116861532-116861582	HAEpiC	amniotic membrane:	n/a

(count:43 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:116841868..116844591-chr9:116846288..116849534,3	MCF-7	breast:
2	chr9:116844498..116845455-chr9:117033807..117034432,3	MCF-7	breast:
3	chr9:116822066..116823998-chr9:116833040..116834650,2	MCF-7	breast:
4	chr9:116850338..116853034-chr9:116856193..116858808,2	K562	blood:
5	chr9:116859675..116862094-chr9:116864175..116866038,2	MCF-7	breast:
6	chr9:116841868..116844591-chr9:116846288..116849534,3	MCF-7	breast:
7	chr9:116837426..116839732-chr9:116847214..116849059,3	MCF-7	breast:
8	chr9:116844821..116845361-chr9:116869981..116870487,2	MCF-7	breast:
9	chr9:116845277..116847223-chr9:116852930..116854750,2	K562	blood:
10	chr9:116821881..116823558-chr9:116825884..116828799,2	K562	blood:
11	chr9:116846273..116847216-chr9:116922173..116922681,2	MCF-7	breast:
12	chr9:116843708..116846188-chr9:116846451..116849353,3	MCF-7	breast:
13	chr9:116850338..116853324-chr9:116855246..116858808,3	K562	blood:
14	chr9:116836828..116838763-chr9:116843693..116846191,2	K562	blood:
15	chr9:116836243..116838411-chr9:116841082..116842914,2	MCF-7	breast:
16	chr9:116844450..116845667-chr9:117052850..117054752,10	K562	blood:
17	chr9:116848752..116850800-chr9:116852040..116854106,2	MCF-7	breast:
18	chr9:116842742..116844725-chr9:116847223..116849817,2	K562	blood:
19	chr9:116844851..116845417-chr9:117067843..117068379,2	MCF-7	breast:
20	chr9:116844247..116845566-chr9:117052560..117054100,7	MCF-7	breast:
21	chr9:116842742..116844725-chr9:116847223..116849817,2	K562	blood:
22	chr9:116844453..116844997-chr9:117033798..117034722,3	MCF-7	breast:
23	chr9:116837426..116839732-chr9:116847214..116849059,3	MCF-7	breast:
24	chr9:116844093..116845109-chr9:117068221..117068772,3	K562	blood:
25	chr9:116844678..116846349-chr9:117050619..117053590,2	MCF-7	breast:
26	chr1:106001832..106002553-chr9:116841509..116842188,2	MCF-7	breast:
27	chr9:116856264..116859004-chr9:116870407..116871935,2	MCF-7	breast:
28	chr9:116845927..116847866-chr9:117052148..117055626,3	MCF-7	breast:
29	chr9:116847982..116849837-chr9:116858325..116860933,2	MCF-7	breast:
30	chr9:116844583..116845499-chr9:117067855..117068993,4	MCF-7	breast:
31	chr9:116837232..116841114-chr9:116841892..116845820,4	MCF-7	breast:
32	chr9:116844518..116845085-chr9:116869930..116870489,2	MCF-7	breast:
33	chr9:116843708..116846188-chr9:116846451..116849353,3	MCF-7	breast:
34	chr9:116845277..116847223-chr9:116852930..116854750,2	K562	blood:
35	chr9:116844543..116845536-chr9:117026114..117026681,2	K562	blood:
36	chr9:116848752..116850800-chr9:116852040..116854106,2	MCF-7	breast:
37	chr9:116846785..116849126-chr9:116861196..116862830,2	MCF-7	breast:
38	chr9:116846559..116847181-chr9:117043604..117044541,2	MCF-7	breast:
39	chr9:116843600..116846294-chr9:117069884..117072218,2	MCF-7	breast:
40	chr9:116637031..116639708-chr9:116859646..116861440,2	MCF-7	breast:
41	chr9:116820042..116822386-chr9:116830008..116831532,2	K562	blood:
42	chr9:116864243..116866474-chr9:116868618..116871598,3	MCF-7	breast:
43	chr9:116849164..116851925-chr9:116855946..116857898,2	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KIF12-1	chr9:116855509-116855777	NONHSAT134365
2	lnc-KIF12-1	chr9:116856166-116856197	NONHSAT134365
3	lnc-KIF12-1	chr9:116848406-116848504	NONHSAT134365

No data

Variant related genes	Relation type
AMBP	TF binding region
KIF12	TF binding region
AMBP	CpG island
KIF12	CpG island
ENSG00000136883	chromatin interactions
ENSG00000106927	chromatin interactions
ENSG00000157657	chromatin interactions
ENSG00000196739	chromatin interactions

Extended variants
information (count: 1729 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:1729 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10817563	chr9:116826842-116826843	Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs143936277	chr9:116826843-116826844	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs550307559	chr9:116826893-116826894	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs532387376	chr9:116826942-116826943	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs5900068	chr9:116826943-116826944	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs573860728	chr9:116826950-116826951	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs397960379	chr9:116826953-116826954	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs536617096	chr9:116826985-116826986	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs564501727	chr9:116826994-116826995	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs139064300	chr9:116827001-116827002	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs370396266	chr9:116827002-116827003	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs199515319	chr9:116827004-116827005	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs529327659	chr9:116827061-116827062	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs10817564	chr9:116827079-116827080	Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs566056522	chr9:116827093-116827094	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs73658326	chr9:116827135-116827136	Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs554025012	chr9:116827184-116827185	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs190451347	chr9:116827245-116827246	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs534839455	chr9:116827274-116827275	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs539570466	chr9:116827297-116827298	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs555858845	chr9:116827300-116827301	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs183041148	chr9:116827310-116827311	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs370698909	chr9:116827320-116827321	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs113007873	chr9:116827333-116827334	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs148672251	chr9:116827334-116827335	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs186917511	chr9:116827377-116827378	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs74458778	chr9:116827391-116827392	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs117885383	chr9:116827447-116827448	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs191818301	chr9:116827449-116827450	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs369669622	chr9:116827475-116827476	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs142173717	chr9:116827522-116827523	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs563789374	chr9:116827578-116827579	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs150760455	chr9:116827590-116827591	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs549494596	chr9:116827593-116827594	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs559527582	chr9:116827599-116827600	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs80252371	chr9:116827600-116827601	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs75160527	chr9:116827655-116827656	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs570695789	chr9:116827682-116827683	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs7020477	chr9:116827760-116827761	Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs184055057	chr9:116827774-116827775	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs187764795	chr9:116827777-116827778	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs370342643	chr9:116827780-116827781	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs535221687	chr9:116827802-116827803	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs548590132	chr9:116827856-116827857	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs375482383	chr9:116827897-116827898	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs555035922	chr9:116827920-116827921	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs77554614	chr9:116827966-116827967	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs534567200	chr9:116828029-116828030	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs139410696	chr9:116828108-116828109	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs567178692	chr9:116828109-116828110	Weak transcription Genic enhancers	n/a	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:631 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:116812200-116827400	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr9:116822000-116832400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr9:116822600-116833400	Genic enhancers	HepG2	liver
4	chr9:116824600-116830600	Genic enhancers	Liver	Liver
5	chr9:116824800-116828200	Weak transcription	Pancreas	Pancrea
6	chr9:116825600-116832000	Weak transcription	Fetal Intestine Small	intestine
7	chr9:116828200-116828400	Enhancers	Ovary	ovary
8	chr9:116828200-116828600	Strong transcription	Pancreas	Pancrea
9	chr9:116828600-116833400	Weak transcription	Pancreas	Pancrea
10	chr9:116830600-116831400	Weak transcription	Liver	Liver
11	chr9:116831400-116836200	Genic enhancers	Liver	Liver
12	chr9:116831800-116832000	Bivalent Enhancer	Ovary	ovary
13	chr9:116832000-116832200	Enhancers	Fetal Intestine Small	intestine
14	chr9:116832000-116832600	Enhancers	Rectal Mucosa Donor 31	rectum
15	chr9:116832200-116832600	Weak transcription	Fetal Intestine Small	intestine
16	chr9:116832400-116832800	Enhancers	Colonic Mucosa	Colon
17	chr9:116832400-116833000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr9:116832400-116833000	Enhancers	Fetal Intestine Large	intestine
19	chr9:116832400-116833000	Enhancers	Sigmoid Colon	Sigmoid Colon
20	chr9:116832400-116835400	Enhancers	Breast Myoepithelial Primary Cells	Breast
21	chr9:116832400-116835400	Enhancers	Esophagus	oesophagus
22	chr9:116832600-116832800	Enhancers	Fetal Intestine Small	intestine
23	chr9:116832800-116833200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr9:116832800-116833600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr9:116832800-116833600	Weak transcription	Fetal Intestine Small	intestine
26	chr9:116832800-116833800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr9:116833000-116833400	Weak transcription	Fetal Intestine Large	intestine
28	chr9:116833000-116833800	Enhancers	HMEC	breast
29	chr9:116833200-116833600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr9:116833200-116833600	Enhancers	NHEK	skin
31	chr9:116833200-116834000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr9:116833200-116834000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
33	chr9:116833200-116835400	Enhancers	Fetal Muscle Leg	muscle
34	chr9:116833400-116833800	Transcr. at gene 5' and 3'	HepG2	liver
35	chr9:116833400-116834800	Enhancers	Fetal Intestine Large	intestine
36	chr9:116833400-116835400	Enhancers	Pancreas	Pancrea
37	chr9:116833400-116835400	Enhancers	Right Ventricle	heart
38	chr9:116833600-116834000	ZNF genes & repeats	Fetal Intestine Small	intestine
39	chr9:116833800-116834400	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr9:116833800-116835000	Genic enhancers	HepG2	liver
41	chr9:116834000-116834600	Enhancers	Fetal Intestine Small	intestine
42	chr9:116834000-116835400	Enhancers	Fetal Muscle Trunk	muscle
43	chr9:116834200-116834800	Enhancers	Colonic Mucosa	Colon
44	chr9:116834200-116834800	Enhancers	Skeletal Muscle Female	skeletal muscle
45	chr9:116834200-116835200	Enhancers	Adipose Nuclei	Adipose
46	chr9:116834200-116835200	Enhancers	Brain Cingulate Gyrus	brain
47	chr9:116834200-116835200	Enhancers	Fetal Lung	lung
48	chr9:116834200-116835200	Enhancers	Right Atrium	heart
49	chr9:116834200-116835400	Enhancers	Stomach Mucosa	stomach
50	chr9:116834400-116834800	Enhancers	Gastric	stomach

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