Variant report

Variant	esv3433695
Chromosome Location	chr9:115822131-115836129
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:315)
CpG islands
(count:305)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:315 , 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	chr9:115834606-115834870	GM12878	blood:	n/a	chr9:115834615-115834628 chr9:115834611-115834620
3	BCL11A	chr9:115832606-115832828	GM12878	blood:	n/a	n/a
4	BCL11A	chr9:115831520-115831701	GM12878	blood:	n/a	n/a
5	BCL11A	chr9:115827158-115827380	GM12878	blood:	n/a	n/a
6	BCL11A	chr9:115826072-115826253	GM12878	blood:	n/a	n/a
7	BCL11A	chr9:115829156-115829420	GM12878	blood:	n/a	chr9:115829161-115829170 chr9:115829165-115829178
8	BCL11A	chr9:115823884-115824048	H1-hESC	embryonic stem cell:	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	chr9:115826329-115826643	GM12878	blood:	n/a	chr9:115826444-115826454
14	EP300	chr9:115824151-115824323	GM12878	blood:	n/a	n/a
15	EP300	chr9:115823546-115823971	GM12878	blood:	n/a	chr9:115823715-115823724
16	EP300	chr9:115829001-115829479	GM12878	blood:	n/a	chr9:115829164-115829173
17	EP300	chr9:115830707-115830959	GM12878	blood:	n/a	n/a
18	EP300	chr9:115825634-115826314	GM12878	blood:	n/a	n/a
19	EP300	chr9:115832153-115832417	GM12878	blood:	n/a	n/a
20	EP300	chr9:115834451-115834929	GM12878	blood:	n/a	chr9:115834614-115834623
21	EP300	chr9:115826705-115826969	GM12878	blood:	n/a	n/a
22	EP300	chr9:115826828-115826998	GM12878	blood:	n/a	n/a
23	EP300	chr9:115832276-115832446	GM12878	blood:	n/a	n/a
24	EP300	chr9:115831777-115832091	GM12878	blood:	n/a	chr9:115831892-115831902
25	EP300	chr9:115831042-115831762	GM12878	blood:	n/a	n/a
26	EP300	chr9:115824630-115824956	GM12878	blood:	n/a	chr9:115824663-115824677
27	EP300	chr9:115835339-115835884	GM12878	blood:	n/a	chr9:115835560-115835574
28	EP300	chr9:115829889-115830555	GM12878	blood:	n/a	chr9:115830110-115830124
29	EP300	chr9:115829600-115829772	GM12878	blood:	n/a	n/a
30	FOSL2	chr9:115830805-115831135	HepG2	liver:	n/a	n/a
31	FOSL2	chr9:115834582-115835415	HepG2	liver:	n/a	n/a
32	FOSL2	chr9:115824519-115824766	HepG2	liver:	n/a	n/a
33	FOSL2	chr9:115823101-115823600	HepG2	liver:	n/a	n/a
34	FOSL2	chr9:115826221-115826534	HepG2	liver:	n/a	n/a
35	FOSL2	chr9:115832531-115833162	HepG2	liver:	n/a	n/a
36	FOSL2	chr9:115831333-115831740	HepG2	liver:	n/a	chr9:115831337-115831346
37	FOSL2	chr9:115825304-115825688	HepG2	liver:	n/a	n/a
38	FOSL2	chr9:115831669-115831982	HepG2	liver:	n/a	n/a
39	FOSL2	chr9:115823640-115824339	HepG2	liver:	n/a	n/a
40	FOSL2	chr9:115826337-115826648	HepG2	liver:	n/a	n/a
41	FOSL2	chr9:115827913-115828297	HepG2	liver:	n/a	n/a
42	FOSL2	chr9:115822464-115822848	HepG2	liver:	n/a	n/a
43	FOSL2	chr9:115826674-115826910	HepG2	liver:	n/a	n/a
44	FOSL2	chr9:115829132-115829965	HepG2	liver:	n/a	n/a
45	FOSL2	chr9:115833361-115833745	HepG2	liver:	n/a	n/a
46	FOSL2	chr9:115828550-115829087	HepG2	liver:	n/a	n/a
47	FOSL2	chr9:115831785-115832096	HepG2	liver:	n/a	n/a
48	FOSL2	chr9:115827083-115827714	HepG2	liver:	n/a	n/a
49	FOSL2	chr9:115832122-115832358	HepG2	liver:	n/a	n/a
50	FOSL2	chr9:115834000-115834537	HepG2	liver:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:115835613-115835663	HCM	heart:	n/a
2	chr9:115833890-115833940	HIPEpiC	eye:	n/a
3	chr9:115825302-115825352	GM06990	blood:	n/a
4	chr9:115824717-115824767	SAEC	small airway:	n/a
5	chr9:115835613-115835663	BJ	skin:	n/a
6	chr9:115825302-115825352	T-47D	breast:	n/a
7	chr9:115835616-115835666	Jurkat	blood:	n/a
8	chr9:115825302-115825352	PFSK-1	brain:	n/a
9	chr9:115835616-115835666	IMR90	lung:	fetal
10	chr9:115824717-115824767	AG04450	lung:	fetal
11	chr9:115835613-115835663	U87	brain:	n/a
12	chr9:115833890-115833940	GM19239	blood:	n/a
13	chr9:115835616-115835666	HRCEpiC	kidney:	n/a
14	chr9:115833890-115833940	BJ	skin:	n/a
15	chr9:115833890-115833940	IMR90	lung:	fetal
16	chr9:115825302-115825352	HPAEpiC	pulmonary alveolar:	n/a
17	chr9:115824717-115824767	GM12892	blood:	n/a
18	chr9:115835613-115835663	ProgFib	skin:	n/a
19	chr9:115824717-115824767	LNCaP	prostate:	n/a
20	chr9:115835616-115835666	SAEC	small airway:	n/a
21	chr9:115835616-115835666	AoSMC	blood vessel:	n/a
22	chr9:115825302-115825352	HRCEpiC	kidney:	n/a
23	chr9:115833890-115833940	HUVEC	blood vessel:	n/a
24	chr9:115835616-115835666	GM12878	blood:	n/a
25	chr9:115835613-115835663	ovcar-3	ovarian:	n/a
26	chr9:115825302-115825352	NT2-D1	testis:	n/a
27	chr9:115835613-115835663	GM12891	blood:	n/a
28	chr9:115833890-115833940	Caco-2	colon:	n/a
29	chr9:115835613-115835663	SAEC	small airway:	n/a
30	chr9:115835613-115835663	A549	lung:	n/a
31	chr9:115835613-115835663	HCPEpiC	choroid plexus:	n/a
32	chr9:115835616-115835666	ECC-1	luminal epithelium:	n/a
33	chr9:115835616-115835666	U87	brain:	n/a
34	chr9:115824717-115824767	Hepatocyte	liver:	n/a
35	chr9:115824717-115824767	HPAEpiC	pulmonary alveolar:	n/a
36	chr9:115825302-115825352	HIPEpiC	eye:	n/a
37	chr9:115835616-115835666	BE2_C	brain:	n/a
38	chr9:115824717-115824767	ECC-1	luminal epithelium:	n/a
39	chr9:115835616-115835666	SK-N-SH	brain:	n/a
40	chr9:115835613-115835663	Caco-2	colon:	n/a
41	chr9:115824717-115824767	MCF10A-Er-Src	breast:	n/a
42	chr9:115833890-115833940	CMK	blood:	n/a
43	chr9:115835613-115835663	Jurkat	blood:	n/a
44	chr9:115825302-115825352	Hepatocyte	liver:	n/a
45	chr9:115835616-115835666	HCF	heart:	n/a
46	chr9:115835613-115835663	HPAEpiC	pulmonary alveolar:	n/a
47	chr9:115835613-115835663	SKMC	muscle:	n/a
48	chr9:115833890-115833940	NB4	blood:	n/a
49	chr9:115824717-115824767	Jurkat	blood:	n/a
50	chr9:115833890-115833940	AG09319	gingival:	n/a

No data

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

Extended variants
information (count: 142 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:142 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs28728218	chr9:115822146-115822147	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs28526807	chr9:115822150-115822151	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs569752423	chr9:115822151-115822152	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs1831438	chr9:115822157-115822158	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs373952647	chr9:115822158-115822159	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs555971603	chr9:115822160-115822161	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs572668043	chr9:115822165-115822166	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs368467625	chr9:115822175-115822176	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs557872732	chr9:115822188-115822189	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs578004801	chr9:115822191-115822192	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs371899878	chr9:115822217-115822218	Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs375083894	chr9:115822223-115822224	Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs543401231	chr9:115822315-115822316	Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs28562001	chr9:115822344-115822345	Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs28436016	chr9:115822401-115822402	Bivalent Enhancer Weak transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs563473544	chr9:115822482-115822483	Bivalent Enhancer Weak transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs137961638	chr9:115822621-115822622	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs187896915	chr9:115822747-115822748	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs113095734	chr9:115822766-115822767	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs573771393	chr9:115822786-115822787	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs62574433	chr9:115822814-115822815	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs112893253	chr9:115822886-115822887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs3897264	chr9:115822998-115822999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs111253902	chr9:115823107-115823108	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs372700682	chr9:115823206-115823207	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs375001346	chr9:115823277-115823278	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs541643657	chr9:115823473-115823474	Weak transcription ZNF genes & repeats Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs201872910	chr9:115823536-115823537	Weak transcription ZNF genes & repeats Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs372991888	chr9:115823555-115823556	Weak transcription ZNF genes & repeats Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs62574435	chr9:115823581-115823582	Weak transcription ZNF genes & repeats Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs376809665	chr9:115823582-115823583	Weak transcription ZNF genes & repeats Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs527598420	chr9:115823657-115823658	ZNF genes & repeats Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs182753880	chr9:115823685-115823686	ZNF genes & repeats Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs28689002	chr9:115823721-115823722	ZNF genes & repeats Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs547621896	chr9:115823738-115823739	ZNF genes & repeats Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs564216165	chr9:115823794-115823795	ZNF genes & repeats Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs369042219	chr9:115823813-115823814	Bivalent Enhancer ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs374152886	chr9:115823815-115823816	Bivalent Enhancer ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs532979944	chr9:115823850-115823851	Bivalent Enhancer ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs200389019	chr9:115823859-115823860	Bivalent Enhancer ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs569790316	chr9:115823888-115823889	Bivalent Enhancer ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs200916804	chr9:115823969-115823970	Bivalent Enhancer ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs60764001	chr9:115824022-115824023	ZNF genes & repeats Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs532357405	chr9:115824023-115824024	ZNF genes & repeats Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs149789561	chr9:115824024-115824025	ZNF genes & repeats Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs62574436	chr9:115824028-115824029	ZNF genes & repeats Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs548202441	chr9:115824047-115824048	ZNF genes & repeats Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs528965966	chr9:115824057-115824058	ZNF genes & repeats Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs371140746	chr9:115824059-115824060	ZNF genes & repeats Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs373864441	chr9:115824084-115824085	ZNF genes & repeats Bivalent Enhancer Enhancers	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:101 , 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	chr9:115819800-115822600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr9:115821000-115822200	Bivalent/Poised TSS	Primary T cells from cord blood	blood
7	chr9:115821000-115822200	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
8	chr9:115821000-115822200	ZNF genes & repeats	Right Atrium	heart
9	chr9:115821000-115822400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr9:115821200-115822200	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
11	chr9:115821200-115822200	Bivalent/Poised TSS	Psoas Muscle	Psoas
12	chr9:115821200-115822400	ZNF genes & repeats	Primary T helper naive cells fromperipheralblood	blood
13	chr9:115821200-115822600	ZNF genes & repeats	Ovary	ovary
14	chr9:115821400-115822200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
15	chr9:115821400-115822200	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood
16	chr9:115821400-115822200	ZNF genes & repeats	Primary T cells effector/memory enriched fromperipheralblood	blood
17	chr9:115821400-115822600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr9:115821600-115822200	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
19	chr9:115821800-115822200	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
20	chr9:115821800-115822200	Bivalent Enhancer	Primary B cells from peripheral blood	blood
21	chr9:115821800-115822200	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
22	chr9:115821800-115822200	Bivalent/Poised TSS	Cortex derived primary cultured neurospheres	brain
23	chr9:115821800-115822200	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr9:115821800-115822200	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr9:115821800-115822200	Bivalent/Poised TSS	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr9:115821800-115822200	Bivalent/Poised TSS	Adipose Nuclei	Adipose
27	chr9:115821800-115822200	Bivalent/Poised TSS	Colon Smooth Muscle	Colon
28	chr9:115821800-115822200	Bivalent/Poised TSS	Fetal Kidney	kidney
29	chr9:115821800-115822200	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
30	chr9:115821800-115822200	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
31	chr9:115821800-115822200	Bivalent/Poised TSS	Thymus	Thymus
32	chr9:115821800-115822400	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
33	chr9:115821800-115822400	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
34	chr9:115821800-115822400	Bivalent/Poised TSS	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr9:115821800-115822400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
36	chr9:115821800-115822400	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
37	chr9:115821800-115822600	Bivalent/Poised TSS	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr9:115821800-115822600	ZNF genes & repeats	HSMM	muscle
39	chr9:115822000-115822200	Bivalent Enhancer	Primary T helper naive cells from peripheral blood	blood
40	chr9:115822000-115822200	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
41	chr9:115822000-115822200	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
42	chr9:115822000-115822400	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr9:115822000-115822400	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr9:115822000-115822400	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr9:115822000-115822400	Bivalent/Poised TSS	Brain Germinal Matrix	brain
46	chr9:115822000-115822400	Flanking Bivalent TSS/Enh	Fetal Brain Female	brain
47	chr9:115822000-115822400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
48	chr9:115822000-115822400	Active TSS	Right Ventricle	heart
49	chr9:115822000-115822400	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
50	chr9:115822200-115822400	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell

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