Variant report

Variant	nsv523287
Chromosome Location	chr9:104191392-104202803
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	chr9:104199996-104200599	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:104194966-104196022	HepG2	liver:	n/a	chr9:104195921-104195937 chr9:104195920-104195936
3	CEBPB	chr9:104200162-104200576	HepG2	liver:	n/a	n/a
4	CEBPB	chr9:104191224-104191429	H1-hESC	embryonic stem cell:	n/a	chr9:104191382-104191395 chr9:104191382-104191395 chr9:104191383-104191394 chr9:104191384-104191393 chr9:104191384-104191393 chr9:104191384-104191393
5	CEBPB	chr9:104191208-104191549	HepG2	liver:	n/a	chr9:104191382-104191395 chr9:104191382-104191395 chr9:104191383-104191394 chr9:104191384-104191393 chr9:104191384-104191393 chr9:104191384-104191393
6	CEBPB	chr9:104191209-104191537	IMR90	lung:	n/a	chr9:104191382-104191395 chr9:104191382-104191395 chr9:104191383-104191394 chr9:104191384-104191393 chr9:104191384-104191393 chr9:104191384-104191393
7	CEBPB	chr9:104191211-104191535	A549	lung:	n/a	chr9:104191382-104191395 chr9:104191382-104191395 chr9:104191383-104191394 chr9:104191384-104191393 chr9:104191384-104191393 chr9:104191384-104191393
8	CHD2	chr9:104199614-104199993	HepG2	liver:	n/a	n/a
9	CTCF	chr9:104195640-104195790	Caco-2	colon:	n/a	n/a
10	CTCF	chr9:104191614-104191673	GM13976	blood:	n/a	n/a
11	CTCF	chr9:104195660-104195810	Caco-2	colon:	n/a	n/a
12	CTCF	chr9:104193720-104193870	HepG2	liver:	n/a	n/a
13	CTCF	chr9:104195680-104195830	HepG2	liver:	n/a	n/a
14	CTCF	chr9:104191684-104191748	Lung_OC	lung:	n/a	n/a
15	CTCF	chr9:104195640-104195790	HepG2	liver:	n/a	n/a
16	ELF1	chr9:104195512-104195875	HepG2	liver:	n/a	n/a
17	EP300	chr9:104195395-104195956	HepG2	liver:	n/a	chr9:104195638-104195651
18	EP300	chr9:104200887-104201129	GM12878	blood:	n/a	chr9:104201028-104201037
19	EP300	chr9:104195466-104195906	HepG2	liver:	n/a	chr9:104195638-104195651
20	EP300	chr9:104199949-104200608	HepG2	liver:	n/a	n/a
21	FOXA1	chr9:104194484-104194819	HepG2	liver:	n/a	n/a
22	FOXA1	chr9:104195509-104195857	HepG2	liver:	n/a	n/a
23	FOXA1	chr9:104195270-104196086	HepG2	liver:	n/a	n/a
24	FOXA1	chr9:104195467-104195869	HepG2	liver:	n/a	n/a
25	FOXA1	chr9:104195368-104196148	HepG2	liver:	n/a	n/a
26	FOXA2	chr9:104195461-104195896	HepG2	liver:	n/a	n/a
27	FOXA2	chr9:104195100-104196146	HepG2	liver:	n/a	n/a
28	GATA3	chr9:104201118-104201414	SH-SY5Y	brain:	n/a	chr9:104201209-104201225
29	GTF2F1	chr9:104202197-104202245	H1-hESC	embryonic stem cell:	n/a	n/a
30	HDAC2	chr9:104195295-104195913	HepG2	liver:	n/a	n/a
31	HDAC2	chr9:104195371-104195901	HepG2	liver:	n/a	n/a
32	HEY1	chr9:104195490-104195920	HepG2	liver:	n/a	n/a
33	HNF4A	chr9:104195505-104195851	HepG2	liver:	n/a	chr9:104195719-104195733 chr9:104195718-104195733 chr9:104195719-104195732 chr9:104195720-104195732
34	HNF4A	chr9:104195482-104195959	HepG2	liver:	n/a	chr9:104195719-104195733 chr9:104195718-104195733 chr9:104195719-104195732 chr9:104195720-104195732
35	HNF4A	chr9:104194519-104194827	HepG2	liver:	n/a	n/a
36	HNF4A	chr9:104194528-104194798	HepG2	liver:	n/a	n/a
37	HNF4A	chr9:104200215-104200621	HepG2	liver:	n/a	chr9:104200467-104200479 chr9:104200466-104200479 chr9:104200466-104200479
38	HNF4G	chr9:104195497-104195924	HepG2	liver:	n/a	chr9:104195719-104195733 chr9:104195719-104195732 chr9:104195720-104195732 chr9:104195717-104195732
39	HNF4G	chr9:104195370-104195985	HepG2	liver:	n/a	chr9:104195719-104195733 chr9:104195719-104195732 chr9:104195720-104195732 chr9:104195717-104195732
40	JUN	chr9:104194333-104194661	HepG2	liver:	n/a	chr9:104194471-104194484
41	JUND	chr9:104195509-104195841	HepG2	liver:	n/a	chr9:104195585-104195597 chr9:104195586-104195596
42	JUND	chr9:104194226-104194630	HepG2	liver:	n/a	n/a
43	JUND	chr9:104195588-104195828	HepG2	liver:	n/a	n/a
44	JUND	chr9:104195538-104195857	HepG2	liver:	n/a	chr9:104195585-104195597 chr9:104195586-104195596
45	MAFF	chr9:104195371-104195852	HepG2	liver:	n/a	chr9:104195578-104195596 chr9:104195584-104195598
46	MAFF	chr9:104192960-104193149	HepG2	liver:	n/a	chr9:104193026-104193044
47	MAFF	chr9:104200052-104200564	HepG2	liver:	n/a	chr9:104200236-104200254 chr9:104200235-104200249
48	MAFK	chr9:104192945-104193114	HepG2	liver:	n/a	chr9:104193028-104193043
49	MAFK	chr9:104200036-104200601	HepG2	liver:	n/a	chr9:104200234-104200250 chr9:104200241-104200252 chr9:104200241-104200252 chr9:104200242-104200253 chr9:104200232-104200252
50	MAFK	chr9:104195404-104195861	HepG2	liver:	n/a	chr9:104195587-104195597 chr9:104195585-104195594

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:104197675-104197725	NT2-D1	testis:	n/a
2	chr9:104197675-104197725	NT2-D1	testis:	n/a
3	chr9:104197675-104197725	HCF	heart:	n/a
4	chr9:104199266-104199316	HAEpiC	amniotic membrane:	n/a
5	chr9:104197886-104197936	HEK293	kidney:	embryo
6	chr9:104197675-104197725	HCT-116	colon:	n/a
7	chr9:104197886-104197936	U87	brain:	n/a
8	chr9:104193952-104194002	HL-60	blood:	n/a
9	chr9:104199266-104199316	Hepatocyte	liver:	n/a
10	chr9:104193952-104194002	HEEpiC	esophagus:	n/a
11	chr9:104198262-104198312	T-47D	breast:	n/a
12	chr9:104193952-104194002	HRE	kidney:	n/a
13	chr9:104193952-104194002	SAEC	small airway:	n/a
14	chr9:104193952-104194002	AG09319	gingival:	n/a
15	chr9:104198262-104198312	GM19239	blood:	n/a
16	chr9:104198262-104198312	HIPEpiC	eye:	n/a
17	chr9:104197886-104197936	GM12878	blood:	n/a
18	chr9:104193952-104194002	A549	lung:	n/a
19	chr9:104193952-104194002	IMR90	lung:	fetal
20	chr9:104198262-104198312	ProgFib	skin:	n/a
21	chr9:104199266-104199316	ovcar-3	ovarian:	n/a
22	chr9:104197886-104197936	A549	lung:	n/a
23	chr9:104197886-104197936	Jurkat	blood:	n/a
24	chr9:104198262-104198312	Caco-2	colon:	n/a
25	chr9:104197886-104197936	LNCaP	prostate:	n/a
26	chr9:104193952-104194002	NH-A	brain:	n/a
27	chr9:104199266-104199316	H1-hESC	embryonic stem cell:	embryo
28	chr9:104197886-104197936	NT2-D1	testis:	n/a
29	chr9:104197675-104197725	AG09319	gingival:	n/a
30	chr9:104197675-104197725	PFSK-1	brain:	n/a
31	chr9:104197886-104197936	ovcar-3	ovarian:	n/a
32	chr9:104199266-104199316	RPTEC	kidney:	n/a
33	chr9:104199266-104199316	ProgFib	skin:	n/a
34	chr9:104198262-104198312	HepG2	liver:	n/a
35	chr9:104193952-104194002	ovcar-3	ovarian:	n/a
36	chr9:104197675-104197725	GM12892	blood:	n/a
37	chr9:104199266-104199316	GM12891	blood:	n/a
38	chr9:104197886-104197936	HPAEpiC	pulmonary alveolar:	n/a
39	chr9:104197886-104197936	AG09319	gingival:	n/a
40	chr9:104199266-104199316	NT2-D1	testis:	n/a
41	chr9:104197886-104197936	ProgFib	skin:	n/a
42	chr9:104198262-104198312	NHDF-neo	bronchial:	n/a
43	chr9:104197675-104197725	ECC-1	luminal epithelium:	n/a
44	chr9:104197886-104197936	ECC-1	luminal epithelium:	n/a
45	chr9:104198262-104198312	HCF	heart:	n/a
46	chr9:104193952-104194002	NHDF-neo	bronchial:	n/a
47	chr9:104197886-104197936	NHBE	bronchial:	n/a
48	chr9:104197886-104197936	GM12892	blood:	n/a
49	chr9:104198262-104198312	GM12892	blood:	n/a
50	chr9:104198262-104198312	HL-60	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:104191772..104193285-chr9:104196452..104198331,2	K562	blood:
2	chr9:104160949..104162500-chr9:104190805..104192507,2	MCF-7	breast:
3	chr9:104192560..104194811-chr9:104200149..104202360,2	K562	blood:
4	chr9:104190256..104192316-chr9:104193462..104195389,2	K562	blood:
5	chr9:104192560..104194189-chr9:104200149..104202095,2	K562	blood:
6	chr9:104192637..104194566-chr9:104195884..104197639,2	MCF-7	breast:
7	chr9:104197118..104199793-chr9:104230175..104232444,2	K562	blood:
8	chr9:104171015..104173390-chr9:104201738..104204667,2	K562	blood:
9	chr9:104192560..104194189-chr9:104200149..104202095,2	K562	blood:
10	chr9:104192560..104194811-chr9:104200149..104202360,2	K562	blood:
11	chr9:104192637..104194566-chr9:104195884..104197639,2	MCF-7	breast:
12	chr9:104189039..104190592-chr9:104201442..104204018,2	K562	blood:
13	chr9:104191772..104193285-chr9:104196452..104198331,2	K562	blood:

Variant related genes	Relation type
ALDOB	TF binding region
ALDOB	CpG island
ENSG00000136870	chromatin interactions
ENSG00000136872	chromatin interactions
ENSG00000225376	chromatin interactions

Extended variants
information (count: 457 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:457 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs550915	chr9:104191392-104191393	Genic enhancers Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs7864833	chr9:104191398-104191399	Genic enhancers Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs200068470	chr9:104191408-104191409	Genic enhancers Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs552828978	chr9:104191421-104191422	Genic enhancers Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs551640	chr9:104191425-104191426	Genic enhancers Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs527932290	chr9:104191429-104191430	Genic enhancers Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs75255910	chr9:104191433-104191434	Genic enhancers Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs75923376	chr9:104191434-104191435	Genic enhancers Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs531552685	chr9:104191474-104191475	Genic enhancers Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs72743343	chr9:104191485-104191486	Genic enhancers Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs567807596	chr9:104191521-104191522	Genic enhancers Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs530220653	chr9:104191582-104191583	Genic enhancers Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs139727291	chr9:104191598-104191599	Genic enhancers Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs570082345	chr9:104191650-104191651	Genic enhancers Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs143017767	chr9:104191663-104191664	Genic enhancers Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs75295708	chr9:104191667-104191668	Genic enhancers Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs139448480	chr9:104191678-104191679	Genic enhancers Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs191436902	chr9:104191680-104191681	Genic enhancers Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs184280777	chr9:104191682-104191683	Genic enhancers Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs188041018	chr9:104191703-104191704	Genic enhancers Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs553697336	chr9:104191733-104191734	Genic enhancers Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs532753208	chr9:104191739-104191740	Genic enhancers Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs573470415	chr9:104191813-104191814	Genic enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs192851595	chr9:104191815-104191816	Genic enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs111241833	chr9:104191832-104191833	Genic enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs185271249	chr9:104191837-104191838	Genic enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs575658291	chr9:104191854-104191855	Genic enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs190170526	chr9:104191903-104191904	Genic enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs565610677	chr9:104191911-104191912	Genic enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs527985839	chr9:104191960-104191961	Genic enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs374413253	chr9:104191996-104191997	Genic enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs118168553	chr9:104192029-104192030	Genic enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs142196987	chr9:104192043-104192044	Genic enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs561489667	chr9:104192046-104192047	Genic enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs200121991	chr9:104192068-104192069	Genic enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs372738117	chr9:104192073-104192074	Genic enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs549682194	chr9:104192079-104192080	Genic enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs200585150	chr9:104192097-104192098	Genic enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs568367333	chr9:104192113-104192114	Genic enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs182003715	chr9:104192118-104192119	Genic enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs375679562	chr9:104192137-104192138	Genic enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs151219186	chr9:104192170-104192171	Genic enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs141267935	chr9:104192182-104192183	Genic enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs118204429	chr9:104192183-104192184	Genic enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs370761101	chr9:104192191-104192192	Genic enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs570143313	chr9:104192192-104192193	Genic enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs200050226	chr9:104192194-104192195	Genic enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs201397971	chr9:104192195-104192196	Genic enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs2854709	chr9:104192199-104192200	Genic enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs149671008	chr9:104192205-104192206	Genic enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
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
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
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
small cell lung cancer	20016488	CNVD
Cardiac fibroma	18329553	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Fukuyama congenital muscular dystrophy	21572526	CNVD
Testicular germ cell tumor	18059402	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Mantle cell lymphoma	19029149	CNVD
Intracranial aneurysm	16715129	CNVD
Neuroblastoma	20406844	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:90 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:104185400-104193200	Strong transcription	Duodenum Mucosa	Duodenum
2	chr9:104187000-104192800	Genic enhancers	Liver	Liver
3	chr9:104188200-104196800	Weak transcription	Left Ventricle	heart
4	chr9:104189200-104191400	Enhancers	HepG2	liver
5	chr9:104189600-104193200	Weak transcription	Pancreas	Pancrea
6	chr9:104190800-104193000	Weak transcription	Fetal Intestine Large	intestine
7	chr9:104191000-104191400	Weak transcription	Fetal Intestine Small	intestine
8	chr9:104191000-104194600	Weak transcription	Stomach Mucosa	stomach
9	chr9:104191400-104192400	Strong transcription	Fetal Intestine Small	intestine
10	chr9:104191400-104192400	Weak transcription	HepG2	liver
11	chr9:104192400-104192800	Genic enhancers	Fetal Intestine Small	intestine
12	chr9:104192400-104195000	Enhancers	HepG2	liver
13	chr9:104192800-104193400	Weak transcription	Fetal Intestine Small	intestine
14	chr9:104192800-104195200	Transcr. at gene 5' and 3'	Liver	Liver
15	chr9:104193000-104196600	Enhancers	Fetal Intestine Large	intestine
16	chr9:104193200-104193400	Genic enhancers	Duodenum Mucosa	Duodenum
17	chr9:104193200-104193400	Enhancers	Small Intestine	intestine
18	chr9:104193200-104195800	Enhancers	Pancreas	Pancrea
19	chr9:104193400-104193800	Enhancers	Fetal Intestine Small	intestine
20	chr9:104193400-104194000	Transcr. at gene 5' and 3'	Duodenum Mucosa	Duodenum
21	chr9:104193400-104196800	Weak transcription	Small Intestine	intestine
22	chr9:104193800-104194600	Flanking Active TSS	Fetal Intestine Small	intestine
23	chr9:104194000-104195000	Active TSS	Duodenum Mucosa	Duodenum
24	chr9:104194000-104197600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
25	chr9:104194600-104195000	Enhancers	Fetal Intestine Small	intestine
26	chr9:104194600-104195200	Enhancers	Stomach Mucosa	stomach
27	chr9:104195000-104195200	Bivalent/Poised TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr9:104195000-104195400	Flanking Active TSS	Duodenum Mucosa	Duodenum
29	chr9:104195000-104195400	Flanking Active TSS	Fetal Intestine Small	intestine
30	chr9:104195000-104195600	Flanking Active TSS	HepG2	liver
31	chr9:104195200-104195400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr9:104195200-104196800	Enhancers	Pancreatic Islets	Pancreatic Islet
33	chr9:104195200-104196800	Weak transcription	Stomach Mucosa	stomach
34	chr9:104195200-104198400	Active TSS	Liver	Liver
35	chr9:104195400-104196000	Enhancers	Fetal Intestine Small	intestine
36	chr9:104195400-104196800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr9:104195400-104198400	Active TSS	Duodenum Mucosa	Duodenum
38	chr9:104195600-104195800	Enhancers	Colon Smooth Muscle	Colon
39	chr9:104195600-104207200	Enhancers	HepG2	liver
40	chr9:104195800-104196800	Weak transcription	Pancreas	Pancrea
41	chr9:104195800-104197400	Weak transcription	Colon Smooth Muscle	Colon
42	chr9:104196000-104198200	Flanking Active TSS	Fetal Intestine Small	intestine
43	chr9:104196400-104198000	Active TSS	Fetal Kidney	kidney
44	chr9:104196600-104197400	Flanking Active TSS	Fetal Intestine Large	intestine
45	chr9:104196600-104197800	Active TSS	Duodenum Smooth Muscle	Duodenum
46	chr9:104196800-104197000	Enhancers	Right Atrium	heart
47	chr9:104196800-104197000	Enhancers	Small Intestine	intestine
48	chr9:104196800-104197200	Enhancers	Colonic Mucosa	Colon
49	chr9:104196800-104197200	Enhancers	Left Ventricle	heart
50	chr9:104196800-104197200	Enhancers	Pancreas	Pancrea

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