Variant report

Variant	nsv1067884
Chromosome Location	chr9:104188775-104195222
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	chr9:104194966-104196022	HepG2	liver:	n/a	chr9:104195921-104195937 chr9:104195920-104195936
2	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
3	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
4	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
5	CEBPB	chr9:104190066-104190419	HepG2	liver:	n/a	n/a
6	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
7	CTCF	chr9:104193720-104193870	HepG2	liver:	n/a	n/a
8	CTCF	chr9:104191684-104191748	Lung_OC	lung:	n/a	n/a
9	CTCF	chr9:104191614-104191673	GM13976	blood:	n/a	n/a
10	CTCF	chr9:104189500-104189650	WERI-Rb-1	eye:	n/a	n/a
11	EP300	chr9:104190266-104190555	GM12878	blood:	n/a	chr9:104190439-104190446
12	FOXA1	chr9:104194484-104194819	HepG2	liver:	n/a	n/a
13	FOXA2	chr9:104190352-104190916	HepG2	liver:	n/a	n/a
14	FOXA2	chr9:104195100-104196146	HepG2	liver:	n/a	n/a
15	HNF4A	chr9:104194528-104194798	HepG2	liver:	n/a	n/a
16	HNF4A	chr9:104194519-104194827	HepG2	liver:	n/a	n/a
17	JUN	chr9:104194333-104194661	HepG2	liver:	n/a	chr9:104194471-104194484
18	JUND	chr9:104194226-104194630	HepG2	liver:	n/a	n/a
19	MAFF	chr9:104192960-104193149	HepG2	liver:	n/a	chr9:104193026-104193044
20	MAFK	chr9:104192938-104193093	HepG2	liver:	n/a	chr9:104193028-104193043
21	MAFK	chr9:104192945-104193114	HepG2	liver:	n/a	chr9:104193028-104193043
22	MAFK	chr9:104195123-104195839	HepG2	liver:	n/a	chr9:104195587-104195597 chr9:104195585-104195594
23	MAZ	chr9:104192927-104193104	HepG2	liver:	n/a	n/a
24	MEF2A	chr9:104190307-104190620	GM12878	blood:	n/a	chr9:104190421-104190442 chr9:104190427-104190438 chr9:104190425-104190440 chr9:104190426-104190441 chr9:104190428-104190437 chr9:104190425-104190441 chr9:104190421-104190442 chr9:104190421-104190442 chr9:104190426-104190440
25	MYBL2	chr9:104194994-104196181	HepG2	liver:	n/a	n/a
26	MYC	chr9:104189810-104189827	MCF-7	breast:	n/a	n/a
27	RCOR1	chr9:104194512-104194650	HepG2	liver:	n/a	n/a
28	RCOR1	chr9:104195145-104195896	HepG2	liver:	n/a	n/a
29	RELA	chr9:104190050-104190974	GM19193	blood:	n/a	n/a
30	RELA	chr9:104190102-104190862	GM19099	blood:	n/a	n/a
31	RELA	chr9:104190132-104190952	GM12891	blood:	n/a	n/a
32	RELA	chr9:104190208-104190690	GM10847	blood:	n/a	n/a
33	RELA	chr9:104190147-104190807	GM12878	blood:	n/a	n/a
34	RELA	chr9:104190217-104191030	GM18505	blood:	n/a	n/a
35	RELA	chr9:104190161-104190813	GM18951	blood:	n/a	n/a
36	RUNX3	chr9:104190166-104190571	GM12878	blood:	n/a	n/a
37	RUNX3	chr9:104190212-104190577	GM12878	blood:	n/a	n/a
38	STAT3	chr9:104190223-104190338	MCF10A-Er-Src	breast:	n/a	n/a
39	TEAD4	chr9:104195093-104196103	HepG2	liver:	n/a	n/a
40	WRNIP1	chr9:104190564-104190695	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:104193952-104194002	RPTEC	kidney:	n/a
2	chr9:104193952-104194002	HL-60	blood:	n/a
3	chr9:104193952-104194002	AoSMC	blood vessel:	n/a
4	chr9:104193952-104194002	MCF-7	breast:	n/a
5	chr9:104193952-104194002	AG04450	lung:	fetal
6	chr9:104193952-104194002	HRCEpiC	kidney:	n/a
7	chr9:104193952-104194002	Jurkat	blood:	n/a
8	chr9:104193952-104194002	PrEC	prostate:	n/a
9	chr9:104193952-104194002	NHDF-neo	bronchial:	n/a
10	chr9:104193952-104194002	LNCaP	prostate:	n/a
11	chr9:104193952-104194002	A549	lung:	n/a
12	chr9:104193952-104194002	SKMC	muscle:	n/a
13	chr9:104193952-104194002	HUVEC	blood vessel:	n/a
14	chr9:104193952-104194002	BJ	skin:	n/a
15	chr9:104193952-104194002	HCPEpiC	choroid plexus:	n/a
16	chr9:104193952-104194002	Caco-2	colon:	n/a
17	chr9:104193952-104194002	HAEpiC	amniotic membrane:	n/a
18	chr9:104193952-104194002	PANC-1	pancreas:	n/a
19	chr9:104193952-104194002	IMR90	lung:	fetal
20	chr9:104193952-104194002	AG09309	skin:	n/a
21	chr9:104193952-104194002	AG09319	gingival:	n/a
22	chr9:104193952-104194002	HCT-116	colon:	n/a
23	chr9:104193952-104194002	NT2-D1	testis:	n/a
24	chr9:104193952-104194002	NB4	blood:	n/a
25	chr9:104193952-104194002	HNPCEpiC	eye:	n/a
26	chr9:104193952-104194002	GM12892	blood:	n/a
27	chr9:104193952-104194002	SK-N-SH_RA	brain:	n/a
28	chr9:104193952-104194002	CMK	blood:	n/a
29	chr9:104193952-104194002	HIPEpiC	eye:	n/a
30	chr9:104193952-104194002	MCF10A-Er-Src	breast:	n/a
31	chr9:104193952-104194002	Hepatocyte	liver:	n/a
32	chr9:104193952-104194002	T-47D	breast:	n/a
33	chr9:104193952-104194002	Hela-S3	cervix:	n/a
34	chr9:104193952-104194002	ECC-1	luminal epithelium:	n/a
35	chr9:104193952-104194002	H1-hESC	embryonic stem cell:	embryo
36	chr9:104193952-104194002	K562	blood:	n/a
37	chr9:104193952-104194002	SK-N-MC	brain:	n/a
38	chr9:104193952-104194002	HepG2	liver:	n/a
39	chr9:104193952-104194002	NHBE	bronchial:	n/a
40	chr9:104193952-104194002	HRE	kidney:	n/a
41	chr9:104193952-104194002	HCF	heart:	n/a
42	chr9:104193952-104194002	GM12891	blood:	n/a
43	chr9:104193952-104194002	SAEC	small airway:	n/a
44	chr9:104193952-104194002	HEK293	kidney:	embryo
45	chr9:104193952-104194002	HEEpiC	esophagus:	n/a
46	chr9:104193952-104194002	ovcar-3	ovarian:	n/a
47	chr9:104193952-104194002	GM19239	blood:	n/a
48	chr9:104193952-104194002	GM06990	blood:	n/a
49	chr9:104193952-104194002	GM12878	blood:	n/a
50	chr9:104193952-104194002	BE2_C	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:104160949..104162500-chr9:104190805..104192507,2	MCF-7	breast:
2	chr9:104192637..104194566-chr9:104195884..104197639,2	MCF-7	breast:
3	chr9:104192560..104194811-chr9:104200149..104202360,2	K562	blood:
4	chr9:104191772..104193285-chr9:104196452..104198331,2	K562	blood:
5	chr9:104173472..104176121-chr9:104187429..104190280,2	MCF-7	breast:
6	chr9:104190256..104192316-chr9:104193462..104195389,2	K562	blood:
7	chr9:104189039..104190592-chr9:104201442..104204018,2	K562	blood:
8	chr9:104192560..104194189-chr9:104200149..104202095,2	K562	blood:

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

Extended variants
information (count: 309 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:309 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs374541456	chr9:104188817-104188818	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs3739721	chr9:104188842-104188843	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs376375686	chr9:104188847-104188848	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs370793608	chr9:104188849-104188850	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs374240733	chr9:104188851-104188852	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs368140282	chr9:104188871-104188872	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs141988626	chr9:104188879-104188880	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs188851404	chr9:104188901-104188902	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs387906226	chr9:104188909-104188910	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs35885472	chr9:104188918-104188919	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs533131687	chr9:104188925-104188926	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs201582514	chr9:104188947-104188948	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs559584742	chr9:104188978-104188979	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs2854705	chr9:104188991-104188992	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs376534311	chr9:104189001-104189002	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs2777350	chr9:104189015-104189016	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs2777351	chr9:104189016-104189017	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs528305537	chr9:104189063-104189064	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs561974572	chr9:104189089-104189090	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs529263838	chr9:104189097-104189098	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs35443504	chr9:104189099-104189100	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs144557386	chr9:104189165-104189166	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs75093537	chr9:104189167-104189168	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs192431066	chr9:104189181-104189182	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs76734656	chr9:104189193-104189194	Genic enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs112202090	chr9:104189203-104189204	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs17773040	chr9:104189209-104189210	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs148613786	chr9:104189223-104189224	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs533211510	chr9:104189313-104189314	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs142088967	chr9:104189316-104189317	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs555551533	chr9:104189362-104189363	Genic enhancers Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs183895835	chr9:104189451-104189452	Genic enhancers Strong transcription Enhancers ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs188230065	chr9:104189453-104189454	Genic enhancers Strong transcription Enhancers ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs570624417	chr9:104189455-104189456	Genic enhancers Strong transcription Enhancers ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs191920560	chr9:104189485-104189486	Genic enhancers Strong transcription Enhancers ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs151175394	chr9:104189491-104189492	Genic enhancers Strong transcription Enhancers ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs537781360	chr9:104189534-104189535	Genic enhancers Strong transcription Enhancers ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs184153664	chr9:104189543-104189544	Genic enhancers Strong transcription Enhancers ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs189663333	chr9:104189544-104189545	Genic enhancers Strong transcription Enhancers ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs140263869	chr9:104189562-104189563	Genic enhancers Strong transcription Enhancers ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs541709699	chr9:104189569-104189570	Genic enhancers Strong transcription Enhancers ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs568330877	chr9:104189573-104189574	Genic enhancers Strong transcription Enhancers ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs561883744	chr9:104189589-104189590	Genic enhancers Strong transcription Enhancers ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs115703955	chr9:104189613-104189614	Enhancers Genic enhancers Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs187730845	chr9:104189650-104189651	Enhancers Genic enhancers Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs569499451	chr9:104189662-104189663	Enhancers Genic enhancers Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs550729556	chr9:104189669-104189670	Enhancers Genic enhancers Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs1929480	chr9:104189680-104189681	Enhancers Genic enhancers Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs200351394	chr9:104189719-104189720	Enhancers Genic enhancers Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs546868362	chr9:104189727-104189728	Enhancers Genic enhancers Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

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

Chromatin state (count:56 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:104179400-104188800	Enhancers	HepG2	liver
2	chr9:104182400-104189600	Weak transcription	Ovary	ovary
3	chr9:104184600-104189200	Weak transcription	Stomach Mucosa	stomach
4	chr9:104185400-104193200	Strong transcription	Duodenum Mucosa	Duodenum
5	chr9:104187000-104192800	Genic enhancers	Liver	Liver
6	chr9:104187400-104189400	Weak transcription	Fetal Intestine Small	intestine
7	chr9:104188200-104189400	Weak transcription	Pancreas	Pancrea
8	chr9:104188200-104196800	Weak transcription	Left Ventricle	heart
9	chr9:104188400-104189400	Weak transcription	Fetal Intestine Large	intestine
10	chr9:104188800-104189200	Weak transcription	HepG2	liver
11	chr9:104189200-104191000	Enhancers	Stomach Mucosa	stomach
12	chr9:104189200-104191400	Enhancers	HepG2	liver
13	chr9:104189400-104189600	Enhancers	Pancreas	Pancrea
14	chr9:104189400-104190000	ZNF genes & repeats	Fetal Intestine Small	intestine
15	chr9:104189400-104190200	Enhancers	Fetal Intestine Large	intestine
16	chr9:104189600-104190000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr9:104189600-104191000	Enhancers	Primary B cells from peripheral blood	blood
18	chr9:104189600-104193200	Weak transcription	Pancreas	Pancrea
19	chr9:104189800-104190000	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr9:104189800-104190000	Enhancers	Sigmoid Colon	Sigmoid Colon
21	chr9:104189800-104190400	Enhancers	GM12878-XiMat	blood
22	chr9:104190000-104190200	Weak transcription	Fetal Intestine Small	intestine
23	chr9:104190200-104190600	Weak transcription	Fetal Intestine Large	intestine
24	chr9:104190200-104191000	Enhancers	Fetal Intestine Small	intestine
25	chr9:104190400-104190800	Flanking Active TSS	GM12878-XiMat	blood
26	chr9:104190600-104190800	Enhancers	Fetal Intestine Large	intestine
27	chr9:104190800-104191200	Enhancers	GM12878-XiMat	blood
28	chr9:104190800-104193000	Weak transcription	Fetal Intestine Large	intestine
29	chr9:104191000-104191400	Weak transcription	Fetal Intestine Small	intestine
30	chr9:104191000-104194600	Weak transcription	Stomach Mucosa	stomach
31	chr9:104191400-104192400	Strong transcription	Fetal Intestine Small	intestine
32	chr9:104191400-104192400	Weak transcription	HepG2	liver
33	chr9:104192400-104192800	Genic enhancers	Fetal Intestine Small	intestine
34	chr9:104192400-104195000	Enhancers	HepG2	liver
35	chr9:104192800-104193400	Weak transcription	Fetal Intestine Small	intestine
36	chr9:104192800-104195200	Transcr. at gene 5' and 3'	Liver	Liver
37	chr9:104193000-104196600	Enhancers	Fetal Intestine Large	intestine
38	chr9:104193200-104193400	Genic enhancers	Duodenum Mucosa	Duodenum
39	chr9:104193200-104193400	Enhancers	Small Intestine	intestine
40	chr9:104193200-104195800	Enhancers	Pancreas	Pancrea
41	chr9:104193400-104193800	Enhancers	Fetal Intestine Small	intestine
42	chr9:104193400-104194000	Transcr. at gene 5' and 3'	Duodenum Mucosa	Duodenum
43	chr9:104193400-104196800	Weak transcription	Small Intestine	intestine
44	chr9:104193800-104194600	Flanking Active TSS	Fetal Intestine Small	intestine
45	chr9:104194000-104195000	Active TSS	Duodenum Mucosa	Duodenum
46	chr9:104194000-104197600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
47	chr9:104194600-104195000	Enhancers	Fetal Intestine Small	intestine
48	chr9:104194600-104195200	Enhancers	Stomach Mucosa	stomach
49	chr9:104195000-104195200	Bivalent/Poised TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr9:104195000-104195400	Flanking Active TSS	Duodenum Mucosa	Duodenum

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