Variant report

Variant	esv3373273
Chromosome Location	chr9:95707031-95711229
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:43)
CpG islands
(count:183)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr9:95709099-95709483	GM12878	blood:	n/a	n/a
2	CEBPB	chr9:95707387-95707426	K562	blood:	n/a	n/a
3	CEBPB	chr9:95708007-95708132	K562	blood:	n/a	chr9:95708043-95708056
4	CEBPB	chr9:95707947-95708131	HepG2	liver:	n/a	chr9:95708043-95708056
5	CEBPB	chr9:95706894-95707085	HepG2	liver:	n/a	n/a
6	CEBPB	chr9:95707365-95707371	HepG2	liver:	n/a	n/a
7	CTCF	chr9:95710220-95710370	GM12873	blood:	n/a	n/a
8	CTCF	chr9:95709236-95709372	GM19239	blood:	n/a	n/a
9	CTCF	chr9:95709980-95710130	SK-N-SH_RA	brain:	n/a	chr9:95710116-95710129 chr9:95710118-95710128 chr9:95709999-95710012
10	CTCF	chr9:95709680-95709830	MCF-7	breast:	n/a	chr9:95709728-95709741
11	CTCF	chr9:95710020-95710170	HEK293	kidney:	n/a	chr9:95710116-95710129 chr9:95710118-95710128
12	CTCF	chr9:95709291-95709357	NHEK	skin:	n/a	n/a
13	FOXA1	chr9:95710729-95711067	T-47D	breast:	n/a	n/a
14	FOXA1	chr9:95710733-95710977	T-47D	breast:	n/a	n/a
15	FOXA1	chr9:95709875-95710043	T-47D	breast:	n/a	n/a
16	FOXA2	chr9:95709726-95710123	A549	lung:	n/a	n/a
17	FOXA2	chr9:95709870-95710203	A549	lung:	n/a	n/a
18	FOXA2	chr9:95710735-95711005	HepG2	liver:	n/a	n/a
19	GATA3	chr9:95710701-95710954	T-47D	breast:	n/a	n/a
20	KAP1	chr9:95708756-95709867	HEK293	kidney:	n/a	n/a
21	MAX	chr9:95709531-95709803	NB4	blood:	n/a	chr9:95709608-95709617
22	MYC	chr9:95709264-95709341	MCF-7	breast:	n/a	n/a
23	MYC	chr9:95709224-95709265	HUVEC	blood vessel:	n/a	n/a
24	MYC	chr9:95709237-95709296	H1-hESC	embryonic stem cell:	n/a	n/a
25	MYC	chr9:95709550-95709750	NB4	blood:	n/a	chr9:95709608-95709617
26	NFATC1	chr9:95709044-95709449	GM12878	blood:	n/a	n/a
27	PBX3	chr9:95709159-95709460	GM12878	blood:	n/a	n/a
28	POLR2A	chr9:95709160-95709372	Gliobla	brain:	n/a	n/a
29	POLR2A	chr9:95709977-95710156	H1-hESC	embryonic stem cell:	n/a	n/a
30	POLR2A	chr9:95709276-95709354	MCF-7	breast:	n/a	n/a
31	POLR2A	chr9:95709162-95709352	H1-hESC	embryonic stem cell:	n/a	n/a
32	POLR2A	chr9:95709565-95710028	ECC-1	luminal epithelium:	n/a	n/a
33	POLR2A	chr9:95709462-95710039	SK-N-MC	brain:	n/a	n/a
34	RCOR1	chr9:95710972-95711070	Hela-S3	cervix:	n/a	n/a
35	REST	chr9:95709052-95711028	H1-neurons	neurons:	n/a	chr9:95709946-95709959 chr9:95709583-95709596 chr9:95709704-95709717
36	RXRA	chr9:95708515-95708684	HepG2	liver:	n/a	n/a
37	SETDB1	chr9:95708739-95708939	U2OS	brain:	n/a	n/a
38	SUZ12	chr9:95708997-95709401	H1-hESC	embryonic stem cell:	n/a	n/a
39	UBTF	chr9:95709649-95709842	K562	blood:	n/a	n/a
40	UBTF	chr9:95709622-95709811	K562	blood:	n/a	n/a
41	ZBTB7A	chr9:95709203-95710581	ECC-1	luminal epithelium:	n/a	n/a
42	ZBTB7A	chr9:95709327-95710495	ECC-1	luminal epithelium:	n/a	n/a
43	ZNF143	chr9:95709735-95709740	H1-hESC	embryonic stem cell:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:95709582-95709632	SKMC	muscle:	n/a
2	chr9:95710046-95710096	HEEpiC	esophagus:	n/a
3	chr9:95710046-95710096	HRCEpiC	kidney:	n/a
4	chr9:95709582-95709632	ECC-1	luminal epithelium:	n/a
5	chr9:95708321-95708371	AG04450	lung:	fetal
6	chr9:95709582-95709632	HPAEpiC	pulmonary alveolar:	n/a
7	chr9:95709582-95709632	AG09309	skin:	n/a
8	chr9:95709582-95709632	HAEpiC	amniotic membrane:	n/a
9	chr9:95709582-95709632	SK-N-MC	brain:	n/a
10	chr9:95708321-95708371	SKMC	muscle:	n/a
11	chr9:95708321-95708371	CMK	blood:	n/a
12	chr9:95710046-95710096	SK-N-SH	brain:	n/a
13	chr9:95709582-95709632	T-47D	breast:	n/a
14	chr9:95709582-95709632	PANC-1	pancreas:	n/a
15	chr9:95709582-95709632	BE2_C	brain:	n/a
16	chr9:95709582-95709632	HCPEpiC	choroid plexus:	n/a
17	chr9:95708321-95708371	PrEC	prostate:	n/a
18	chr9:95708321-95708371	BE2_C	brain:	n/a
19	chr9:95710046-95710096	NHBE	bronchial:	n/a
20	chr9:95708321-95708371	HRCEpiC	kidney:	n/a
21	chr9:95710046-95710096	HCF	heart:	n/a
22	chr9:95710046-95710096	HMEC	breast:	n/a
23	chr9:95710046-95710096	GM12878	blood:	n/a
24	chr9:95708321-95708371	NB4	blood:	n/a
25	chr9:95709582-95709632	BJ	skin:	n/a
26	chr9:95709582-95709632	SK-N-SH_RA	brain:	n/a
27	chr9:95710046-95710096	HepG2	liver:	n/a
28	chr9:95709582-95709632	HRCEpiC	kidney:	n/a
29	chr9:95710046-95710096	U87	brain:	n/a
30	chr9:95710046-95710096	AG09309	skin:	n/a
31	chr9:95709582-95709632	NB4	blood:	n/a
32	chr9:95710046-95710096	HPAEpiC	pulmonary alveolar:	n/a
33	chr9:95709582-95709632	NH-A	brain:	n/a
34	chr9:95708321-95708371	T-47D	breast:	n/a
35	chr9:95708321-95708371	AoSMC	blood vessel:	n/a
36	chr9:95708321-95708371	HEEpiC	esophagus:	n/a
37	chr9:95709582-95709632	HCF	heart:	n/a
38	chr9:95709582-95709632	IMR90	lung:	fetal
39	chr9:95708321-95708371	HL-60	blood:	n/a
40	chr9:95708321-95708371	HRE	kidney:	n/a
41	chr9:95708321-95708371	U87	brain:	n/a
42	chr9:95710046-95710096	Hela-S3	cervix:	n/a
43	chr9:95710046-95710096	LNCaP	prostate:	n/a
44	chr9:95709582-95709632	MCF10A-Er-Src	breast:	n/a
45	chr9:95710046-95710096	HCM	heart:	n/a
46	chr9:95708321-95708371	HepG2	liver:	n/a
47	chr9:95709582-95709632	NHBE	bronchial:	n/a
48	chr9:95710046-95710096	HCPEpiC	choroid plexus:	n/a
49	chr9:95709582-95709632	HEK293	kidney:	embryo
50	chr9:95710046-95710096	BJ	skin:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr9:95708784..95711358-chr9:96213029..96214881,2	K562	blood:
2	chr9:95706988..95710231-chr9:95710858..95713457,3	MCF-7	breast:
3	chr9:95706512..95708726-chr9:95712017..95714192,2	K562	blood:

No data

Variant related genes	Relation type
FGD3	TF binding region
FGD3	CpG island
ENSG00000048828	chromatin interactions
ENSG00000188938	chromatin interactions
ENSG00000127084	chromatin interactions

Extended variants
information (count: 153 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:153 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs557580939	chr9:95707047-95707048	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs567357657	chr9:95707106-95707107	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs369241697	chr9:95707160-95707161	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs540097052	chr9:95707179-95707180	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs558181635	chr9:95707180-95707181	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs573513972	chr9:95707199-95707200	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs540209448	chr9:95707200-95707201	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs551241727	chr9:95707260-95707261	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs555385105	chr9:95707265-95707266	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs573783647	chr9:95707277-95707278	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs375593786	chr9:95707287-95707288	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs544311596	chr9:95707325-95707326	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs34953814	chr9:95707332-95707333	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs530641813	chr9:95707337-95707338	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs546046817	chr9:95707365-95707366	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs74971778	chr9:95707402-95707403	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs528424206	chr9:95707407-95707408	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs562399690	chr9:95707445-95707446	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs146860760	chr9:95707527-95707528	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs536212212	chr9:95707568-95707569	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs112892562	chr9:95707611-95707612	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs142953373	chr9:95707612-95707613	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs548951743	chr9:95707627-95707628	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs539627918	chr9:95707632-95707633	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs558356417	chr9:95707633-95707634	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs567047123	chr9:95707634-95707635	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs75996881	chr9:95707670-95707671	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs534258666	chr9:95707672-95707673	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs555299143	chr9:95707683-95707684	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs573704062	chr9:95707732-95707733	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs544274730	chr9:95707739-95707740	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs556399366	chr9:95707771-95707772	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs578075313	chr9:95707862-95707863	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs567279878	chr9:95707876-95707877	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs76540086	chr9:95707877-95707878	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs117648701	chr9:95707880-95707881	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs528386575	chr9:95707893-95707894	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs76276266	chr9:95707896-95707897	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs561638759	chr9:95707931-95707932	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs528912511	chr9:95707938-95707939	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs550583274	chr9:95708019-95708020	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs551173981	chr9:95708022-95708023	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs534706280	chr9:95708029-95708030	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs552837464	chr9:95708032-95708033	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs151120174	chr9:95708045-95708046	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs533092737	chr9:95708047-95708048	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs577742270	chr9:95708093-95708094	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs551670441	chr9:95708127-95708128	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs140920245	chr9:95708145-95708146	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs61137937	chr9:95708149-95708150	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

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
Bipolar disorder	18458673	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Biliary cancer	19435499	CNVD
small cell lung cancer	20016488	CNVD
Intracranial aneurysm	16715129	CNVD
Cardiac fibroma	18329553	CNVD
Mental retardation	21693067	CNVD
Breast cancer	17133270	CNVD
Basal cell nevus syndrome	21572526	CNVD
Mental retardation	19951919	CNVD
Retinoblastoma	22278416	CNVD
9q22.3 microdeletion syndrome	22283845	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Microcephaly	18830227	CNVD
overgrowth syndrome	16570072	CNVD

Chromatin state (count:421 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:95702000-95709400	Weak transcription	Right Atrium	heart
2	chr9:95703400-95708200	Weak transcription	Brain Germinal Matrix	brain
3	chr9:95703600-95709200	Weak transcription	Spleen	Spleen
4	chr9:95704400-95707400	Enhancers	Primary neutrophils fromperipheralblood	blood
5	chr9:95704600-95709200	Weak transcription	HSMMtube	muscle
6	chr9:95705800-95708800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr9:95705800-95709000	Weak transcription	Fetal Brain Female	brain
8	chr9:95705800-95709200	Weak transcription	Esophagus	oesophagus
9	chr9:95706000-95708800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
10	chr9:95706000-95708800	Weak transcription	Primary T helper cells PMA-I stimulated	--
11	chr9:95706000-95708800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
12	chr9:95706400-95707200	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr9:95706400-95709000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr9:95706400-95709200	Weak transcription	HSMM	muscle
15	chr9:95706400-95709400	Weak transcription	Psoas Muscle	Psoas
16	chr9:95706800-95707400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr9:95707000-95707400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr9:95707000-95708400	Enhancers	Fetal Muscle Trunk	muscle
19	chr9:95707000-95708400	Enhancers	Fetal Muscle Leg	muscle
20	chr9:95707200-95707400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
21	chr9:95707200-95707400	Enhancers	Ovary	ovary
22	chr9:95707200-95707400	Enhancers	Right Ventricle	heart
23	chr9:95707200-95707400	Enhancers	Skeletal Muscle Male	skeletal muscle
24	chr9:95707400-95708200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr9:95707400-95709200	Weak transcription	Skeletal Muscle Male	skeletal muscle
26	chr9:95707600-95709600	Weak transcription	Ovary	ovary
27	chr9:95707800-95708000	Enhancers	Fetal Brain Male	brain
28	chr9:95707800-95708600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
29	chr9:95708000-95709000	Weak transcription	Fetal Brain Male	brain
30	chr9:95708200-95708400	Enhancers	Brain Germinal Matrix	brain
31	chr9:95708200-95709200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr9:95708200-95709200	ZNF genes & repeats	Primary Natural Killer cells fromperipheralblood	blood
33	chr9:95708400-95708800	Weak transcription	Brain Germinal Matrix	brain
34	chr9:95708400-95709000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
35	chr9:95708400-95709000	Enhancers	Primary T helper naive cells from peripheral blood	blood
36	chr9:95708400-95709200	Weak transcription	Fetal Muscle Trunk	muscle
37	chr9:95708400-95709200	Weak transcription	Right Ventricle	heart
38	chr9:95708600-95709000	Enhancers	Primary T cells fromperipheralblood	blood
39	chr9:95708800-95709000	Enhancers	Primary T cells from cord blood	blood
40	chr9:95708800-95709000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
41	chr9:95708800-95709000	Enhancers	Primary T helper cells PMA-I stimulated	--
42	chr9:95708800-95709000	Enhancers	Primary T helper cells fromperipheralblood	blood
43	chr9:95708800-95709000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
44	chr9:95708800-95709000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
45	chr9:95708800-95709000	Enhancers	Primary T killer memory cells from peripheral blood	blood
46	chr9:95708800-95709000	Enhancers	Brain Germinal Matrix	brain
47	chr9:95708800-95709200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
48	chr9:95708800-95709200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
49	chr9:95708800-95709200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
50	chr9:95709000-95709200	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links