Variant report

Variant	esv3437370
Chromosome Location	chr9:115821231-115835029
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:302)
CpG islands
(count:306)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:302 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr9:115823819-115824137	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCL11A	chr9:115827158-115827380	GM12878	blood:	n/a	n/a
3	BCL11A	chr9:115831520-115831701	GM12878	blood:	n/a	n/a
4	BCL11A	chr9:115834606-115834870	GM12878	blood:	n/a	chr9:115834615-115834628 chr9:115834611-115834620
5	BCL11A	chr9:115823884-115824048	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL11A	chr9:115832606-115832828	GM12878	blood:	n/a	n/a
7	BCL11A	chr9:115829156-115829420	GM12878	blood:	n/a	chr9:115829161-115829170 chr9:115829165-115829178
8	BCL11A	chr9:115826072-115826253	GM12878	blood:	n/a	n/a
9	CHD2	chr9:115825423-115825439	Hela-S3	cervix:	n/a	n/a
10	CTBP2	chr9:115823828-115824165	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTCF	chr9:115823840-115823990	GM12873	blood:	n/a	n/a
12	ELK1	chr9:115825281-115825333	Hela-S3	cervix:	n/a	n/a
13	EP300	chr9:115829001-115829479	GM12878	blood:	n/a	chr9:115829164-115829173
14	EP300	chr9:115831777-115832091	GM12878	blood:	n/a	chr9:115831892-115831902
15	EP300	chr9:115826705-115826969	GM12878	blood:	n/a	n/a
16	EP300	chr9:115823546-115823971	GM12878	blood:	n/a	chr9:115823715-115823724
17	EP300	chr9:115830707-115830959	GM12878	blood:	n/a	n/a
18	EP300	chr9:115824151-115824323	GM12878	blood:	n/a	n/a
19	EP300	chr9:115834451-115834929	GM12878	blood:	n/a	chr9:115834614-115834623
20	EP300	chr9:115825634-115826314	GM12878	blood:	n/a	n/a
21	EP300	chr9:115826329-115826643	GM12878	blood:	n/a	chr9:115826444-115826454
22	EP300	chr9:115829600-115829772	GM12878	blood:	n/a	n/a
23	EP300	chr9:115824630-115824956	GM12878	blood:	n/a	chr9:115824663-115824677
24	EP300	chr9:115832153-115832417	GM12878	blood:	n/a	n/a
25	EP300	chr9:115829889-115830555	GM12878	blood:	n/a	chr9:115830110-115830124
26	EP300	chr9:115826828-115826998	GM12878	blood:	n/a	n/a
27	EP300	chr9:115832276-115832446	GM12878	blood:	n/a	n/a
28	EP300	chr9:115831042-115831762	GM12878	blood:	n/a	n/a
29	FOSL2	chr9:115831785-115832096	HepG2	liver:	n/a	n/a
30	FOSL2	chr9:115823101-115823600	HepG2	liver:	n/a	n/a
31	FOSL2	chr9:115832531-115833162	HepG2	liver:	n/a	n/a
32	FOSL2	chr9:115831669-115831982	HepG2	liver:	n/a	n/a
33	FOSL2	chr9:115822464-115822848	HepG2	liver:	n/a	n/a
34	FOSL2	chr9:115827913-115828297	HepG2	liver:	n/a	n/a
35	FOSL2	chr9:115826674-115826910	HepG2	liver:	n/a	n/a
36	FOSL2	chr9:115827083-115827714	HepG2	liver:	n/a	n/a
37	FOSL2	chr9:115834582-115835415	HepG2	liver:	n/a	n/a
38	FOSL2	chr9:115826221-115826534	HepG2	liver:	n/a	n/a
39	FOSL2	chr9:115829132-115829965	HepG2	liver:	n/a	n/a
40	FOSL2	chr9:115825304-115825688	HepG2	liver:	n/a	n/a
41	FOSL2	chr9:115828550-115829087	HepG2	liver:	n/a	n/a
42	FOSL2	chr9:115832122-115832358	HepG2	liver:	n/a	n/a
43	FOSL2	chr9:115834000-115834537	HepG2	liver:	n/a	n/a
44	FOSL2	chr9:115825885-115826292	HepG2	liver:	n/a	chr9:115825889-115825898
45	FOSL2	chr9:115824519-115824766	HepG2	liver:	n/a	n/a
46	FOSL2	chr9:115833361-115833745	HepG2	liver:	n/a	n/a
47	FOSL2	chr9:115826337-115826648	HepG2	liver:	n/a	n/a
48	FOSL2	chr9:115823640-115824339	HepG2	liver:	n/a	n/a
49	FOSL2	chr9:115830805-115831135	HepG2	liver:	n/a	n/a
50	FOSL2	chr9:115829992-115830556	HepG2	liver:	n/a	n/a

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:115825302-115825352	AG09309	skin:	n/a
2	chr9:115825302-115825352	AG09309	skin:	n/a
3	chr9:115822072-115822122	NHDF-neo	bronchial:	n/a
4	chr9:115825302-115825352	Hepatocyte	liver:	n/a
5	chr9:115833890-115833940	HCPEpiC	choroid plexus:	n/a
6	chr9:115824717-115824767	NB4	blood:	n/a
7	chr9:115822072-115822122	SK-N-MC	brain:	n/a
8	chr9:115824717-115824767	LNCaP	prostate:	n/a
9	chr9:115825302-115825352	HNPCEpiC	eye:	n/a
10	chr9:115821352-115821402	NHBE	bronchial:	n/a
11	chr9:115824717-115824767	HUVEC	blood vessel:	n/a
12	chr9:115833890-115833940	K562	blood:	n/a
13	chr9:115821352-115821402	HCT-116	colon:	n/a
14	chr9:115833890-115833940	A549	lung:	n/a
15	chr9:115833890-115833940	GM06990	blood:	n/a
16	chr9:115822072-115822122	HIPEpiC	eye:	n/a
17	chr9:115822072-115822122	IMR90	lung:	fetal
18	chr9:115821352-115821402	Caco-2	colon:	n/a
19	chr9:115825302-115825352	HUVEC	blood vessel:	n/a
20	chr9:115821352-115821402	HMEC	breast:	n/a
21	chr9:115824717-115824767	A549	lung:	n/a
22	chr9:115821352-115821402	A549	lung:	n/a
23	chr9:115822072-115822122	U87	brain:	n/a
24	chr9:115821352-115821402	AG10803	skin:	n/a
25	chr9:115825302-115825352	GM19239	blood:	n/a
26	chr9:115824717-115824767	HCF	heart:	n/a
27	chr9:115822072-115822122	NHBE	bronchial:	n/a
28	chr9:115824717-115824767	ECC-1	luminal epithelium:	n/a
29	chr9:115821352-115821402	HAEpiC	amniotic membrane:	n/a
30	chr9:115833890-115833940	HCT-116	colon:	n/a
31	chr9:115825302-115825352	Jurkat	blood:	n/a
32	chr9:115822072-115822122	HMEC	breast:	n/a
33	chr9:115822072-115822122	SAEC	small airway:	n/a
34	chr9:115824717-115824767	BE2_C	brain:	n/a
35	chr9:115833890-115833940	MCF10A-Er-Src	breast:	n/a
36	chr9:115822072-115822122	HUVEC	blood vessel:	n/a
37	chr9:115822072-115822122	PANC-1	pancreas:	n/a
38	chr9:115821352-115821402	SAEC	small airway:	n/a
39	chr9:115825302-115825352	AG09319	gingival:	n/a
40	chr9:115833890-115833940	U87	brain:	n/a
41	chr9:115825302-115825352	HAEpiC	amniotic membrane:	n/a
42	chr9:115821352-115821402	ovcar-3	ovarian:	n/a
43	chr9:115824717-115824767	HNPCEpiC	eye:	n/a
44	chr9:115822072-115822122	A549	lung:	n/a
45	chr9:115824717-115824767	HRCEpiC	kidney:	n/a
46	chr9:115824717-115824767	AG09319	gingival:	n/a
47	chr9:115821352-115821402	Hepatocyte	liver:	n/a
48	chr9:115822072-115822122	NT2-D1	testis:	n/a
49	chr9:115824717-115824767	HRPEpiC	eye:	n/a
50	chr9:115821352-115821402	NHDF-neo	bronchial:	n/a

No data

Variant related genes	Relation type
ZFP37	TF binding region
ZFP37	CpG island

Extended variants
information (count: 246 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:246 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138345641	chr9:115821237-115821238	ZNF genes & repeats Bivalent/Poised TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs573111724	chr9:115821239-115821240	ZNF genes & repeats Bivalent/Poised TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs187450614	chr9:115821246-115821247	ZNF genes & repeats Bivalent/Poised TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs527613055	chr9:115821251-115821252	ZNF genes & repeats Bivalent/Poised TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs375410554	chr9:115821257-115821258	ZNF genes & repeats Bivalent/Poised TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs575197873	chr9:115821262-115821263	ZNF genes & repeats Bivalent/Poised TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs543795562	chr9:115821268-115821269	ZNF genes & repeats Bivalent/Poised TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs560687386	chr9:115821270-115821271	ZNF genes & repeats Bivalent/Poised TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs574175138	chr9:115821283-115821284	ZNF genes & repeats Bivalent/Poised TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs142837763	chr9:115821292-115821293	ZNF genes & repeats Bivalent/Poised TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs547192346	chr9:115821309-115821310	ZNF genes & repeats Bivalent/Poised TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs75659210	chr9:115821317-115821318	ZNF genes & repeats Bivalent/Poised TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs368137694	chr9:115821324-115821325	ZNF genes & repeats Bivalent/Poised TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs371700652	chr9:115821328-115821329	ZNF genes & repeats Bivalent/Poised TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs532847461	chr9:115821335-115821336	ZNF genes & repeats Bivalent/Poised TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs551283553	chr9:115821350-115821351	ZNF genes & repeats Bivalent/Poised TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs150144519	chr9:115821374-115821375	ZNF genes & repeats Bivalent/Poised TSS Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
18	rs563190149	chr9:115821375-115821376	ZNF genes & repeats Bivalent/Poised TSS Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
19	rs571193772	chr9:115821376-115821377	ZNF genes & repeats Bivalent/Poised TSS Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
20	rs531780592	chr9:115821378-115821379	ZNF genes & repeats Bivalent/Poised TSS Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
21	rs80303174	chr9:115821395-115821396	ZNF genes & repeats Bivalent/Poised TSS Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
22	rs386737754	chr9:115821413-115821414	Bivalent/Poised TSS ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs191076574	chr9:115821428-115821429	Bivalent/Poised TSS ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs534257402	chr9:115821430-115821431	Bivalent/Poised TSS ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs111618248	chr9:115821437-115821438	Bivalent/Poised TSS ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs138571775	chr9:115821449-115821450	Bivalent/Poised TSS ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs538824821	chr9:115821457-115821458	Bivalent/Poised TSS ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs558619602	chr9:115821476-115821477	Bivalent/Poised TSS ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs10759623	chr9:115821485-115821486	Bivalent/Poised TSS ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs535513325	chr9:115821498-115821499	Bivalent/Poised TSS ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs372334688	chr9:115821509-115821510	Bivalent/Poised TSS ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs548815580	chr9:115821515-115821516	Bivalent/Poised TSS ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs10541987	chr9:115821525-115821526	Bivalent/Poised TSS ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs3220385	chr9:115821526-115821527	Bivalent/Poised TSS ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs201770689	chr9:115821534-115821535	Bivalent/Poised TSS ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs58403011	chr9:115821561-115821562	Bivalent/Poised TSS ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs545057295	chr9:115821571-115821572	Bivalent/Poised TSS ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs377308568	chr9:115821598-115821599	Bivalent/Poised TSS ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs149324454	chr9:115821599-115821600	Bivalent/Poised TSS ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs372481364	chr9:115821608-115821609	Bivalent/Poised TSS ZNF genes & repeats Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs539898668	chr9:115821613-115821614	Bivalent/Poised TSS ZNF genes & repeats Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs373263335	chr9:115821614-115821615	Bivalent/Poised TSS ZNF genes & repeats Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs183706695	chr9:115821637-115821638	Bivalent/Poised TSS ZNF genes & repeats Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs187981340	chr9:115821638-115821639	Bivalent/Poised TSS ZNF genes & repeats Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs111441672	chr9:115821639-115821640	Bivalent/Poised TSS ZNF genes & repeats Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs192609185	chr9:115821648-115821649	Bivalent/Poised TSS ZNF genes & repeats Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs532021273	chr9:115821669-115821670	Bivalent/Poised TSS ZNF genes & repeats Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs73546528	chr9:115821671-115821672	Bivalent/Poised TSS ZNF genes & repeats Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs545480941	chr9:115821685-115821686	Bivalent/Poised TSS ZNF genes & repeats Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs376793020	chr9:115821695-115821696	Bivalent/Poised TSS ZNF genes & repeats Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

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
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Bladder cancer	21909424	CNVD

Chromatin state (count:118 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:115793000-115822200	ZNF genes & repeats	Liver	Liver
2	chr9:115817600-115822400	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
3	chr9:115817800-115822400	ZNF genes & repeats	Primary hematopoietic stem cells	blood
4	chr9:115818200-115822600	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
5	chr9:115819800-115821800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
6	chr9:115819800-115822600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr9:115820400-115822000	ZNF genes & repeats	Aorta	Aorta
8	chr9:115821000-115822000	ZNF genes & repeats	Pancreas	Pancrea
9	chr9:115821000-115822000	ZNF genes & repeats	Right Ventricle	heart
10	chr9:115821000-115822200	Bivalent/Poised TSS	Primary T cells from cord blood	blood
11	chr9:115821000-115822200	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
12	chr9:115821000-115822200	ZNF genes & repeats	Right Atrium	heart
13	chr9:115821000-115822400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr9:115821200-115821800	ZNF genes & repeats	Adipose Nuclei	Adipose
15	chr9:115821200-115822200	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
16	chr9:115821200-115822200	Bivalent/Poised TSS	Psoas Muscle	Psoas
17	chr9:115821200-115822400	ZNF genes & repeats	Primary T helper naive cells fromperipheralblood	blood
18	chr9:115821200-115822600	ZNF genes & repeats	Ovary	ovary
19	chr9:115821400-115822200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
20	chr9:115821400-115822200	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood
21	chr9:115821400-115822200	ZNF genes & repeats	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr9:115821400-115822600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr9:115821600-115821800	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr9:115821600-115821800	Bivalent/Poised TSS	Brain Germinal Matrix	brain
25	chr9:115821600-115822000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
26	chr9:115821600-115822000	Bivalent/Poised TSS	Fetal Brain Female	brain
27	chr9:115821600-115822200	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
28	chr9:115821800-115822000	Bivalent Enhancer	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr9:115821800-115822000	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
30	chr9:115821800-115822000	Flanking Bivalent TSS/Enh	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr9:115821800-115822000	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr9:115821800-115822000	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
33	chr9:115821800-115822000	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr9:115821800-115822000	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr9:115821800-115822000	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
36	chr9:115821800-115822200	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
37	chr9:115821800-115822200	Bivalent Enhancer	Primary B cells from peripheral blood	blood
38	chr9:115821800-115822200	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
39	chr9:115821800-115822200	Bivalent/Poised TSS	Cortex derived primary cultured neurospheres	brain
40	chr9:115821800-115822200	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr9:115821800-115822200	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr9:115821800-115822200	Bivalent/Poised TSS	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr9:115821800-115822200	Bivalent/Poised TSS	Adipose Nuclei	Adipose
44	chr9:115821800-115822200	Bivalent/Poised TSS	Colon Smooth Muscle	Colon
45	chr9:115821800-115822200	Bivalent/Poised TSS	Fetal Kidney	kidney
46	chr9:115821800-115822200	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
47	chr9:115821800-115822200	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
48	chr9:115821800-115822200	Bivalent/Poised TSS	Thymus	Thymus
49	chr9:115821800-115822400	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
50	chr9:115821800-115822400	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links