Variant report

Variant	esv9886
Chromosome Location	chr17:45142849-45153796
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:898)
CpG islands
(count:123)
Chromatin interactive
region (count:7)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:898 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:45144743-45145166	K562	blood:	n/a	n/a
2	ARID3A	chr17:45144527-45145208	HepG2	liver:	n/a	n/a
3	ATF1	chr17:45148562-45148592	K562	blood:	n/a	n/a
4	ATF2	chr17:45144587-45145135	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr17:45144651-45145146	GM12878	blood:	n/a	n/a
6	ATF2	chr17:45144604-45145036	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr17:45144575-45145188	GM12878	blood:	n/a	n/a
8	ATF3	chr17:45144278-45145192	A549	lung:	n/a	n/a
9	ATF3	chr17:45144521-45145080	A549	lung:	n/a	n/a
10	ATF3	chr17:45144719-45145135	K562	blood:	n/a	n/a
11	BACH1	chr17:45144464-45144994	K562	blood:	n/a	n/a
12	BATF	chr17:45144747-45145054	GM12878	blood:	n/a	n/a
13	BCL11A	chr17:45144770-45145045	GM12878	blood:	n/a	n/a
14	BCL11A	chr17:45144678-45144962	GM12878	blood:	n/a	n/a
15	BCL3	chr17:45143945-45145197	A549	lung:	n/a	n/a
16	BCL3	chr17:45144478-45145168	A549	lung:	n/a	n/a
17	BCL3	chr17:45144494-45145057	GM12878	blood:	n/a	n/a
18	BCLAF1	chr17:45144518-45145177	K562	blood:	n/a	n/a
19	BCLAF1	chr17:45144545-45145178	K562	blood:	n/a	n/a
20	BCLAF1	chr17:45144096-45145119	GM12878	blood:	n/a	n/a
21	BCLAF1	chr17:45144491-45145085	GM12878	blood:	n/a	n/a
22	BHLHE40	chr17:45144674-45145149	GM12878	blood:	n/a	n/a
23	BHLHE40	chr17:45144608-45145047	K562	blood:	n/a	n/a
24	BHLHE40	chr17:45147784-45147837	A549	lung:	n/a	n/a
25	BRCA1	chr17:45147769-45147988	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr17:45144647-45144987	HepG2	liver:	n/a	n/a
27	BRCA1	chr17:45144688-45145138	Hela-S3	cervix:	n/a	n/a
28	CBX3	chr17:45144515-45145100	K562	blood:	n/a	n/a
29	CBX3	chr17:45144579-45145091	K562	blood:	n/a	n/a
30	CBX3	chr17:45148405-45148864	K562	blood:	n/a	n/a
31	CCNT2	chr17:45144623-45145013	K562	blood:	n/a	n/a
32	CEBPB	chr17:45144772-45145003	GM12878	blood:	n/a	n/a
33	CEBPB	chr17:45147780-45147886	A549	lung:	n/a	n/a
34	CEBPB	chr17:45147660-45147980	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr17:45144569-45145210	A549	lung:	n/a	n/a
36	CEBPB	chr17:45148891-45149068	K562	blood:	n/a	n/a
37	CEBPB	chr17:45153563-45153819	IMR90	lung:	n/a	n/a
38	CEBPB	chr17:45144728-45145111	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr17:45144882-45145097	K562	blood:	n/a	n/a
40	CEBPB	chr17:45144723-45145121	K562	blood:	n/a	n/a
41	CEBPB	chr17:45144692-45145088	ECC-1	luminal epithelium:	n/a	n/a
42	CEBPB	chr17:45144673-45144876	HepG2	liver:	n/a	n/a
43	CEBPB	chr17:45144767-45145096	HepG2	liver:	n/a	n/a
44	CEBPD	chr17:45144653-45145011	HepG2	liver:	n/a	n/a
45	CEBPD	chr17:45144588-45145056	HepG2	liver:	n/a	n/a
46	CEBPD	chr17:45144558-45145104	K562	blood:	n/a	n/a
47	CHD1	chr17:45143917-45145182	IMR90	lung:	n/a	n/a
48	CHD1	chr17:45144471-45145003	GM12878	blood:	n/a	n/a
49	CHD2	chr17:45147684-45147884	Hela-S3	cervix:	n/a	n/a
50	CHD2	chr17:45144654-45145123	GM12878	blood:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:45144857-45144907	AG04450	lung:	fetal
2	chr17:45144857-45144907	AG04450	lung:	fetal
3	chr17:45144857-45144907	SAEC	small airway:	n/a
4	chr17:45144857-45144907	RPTEC	kidney:	n/a
5	chr17:45144857-45144907	GM06990	blood:	n/a
6	chr17:45144857-45144907	NB4	blood:	n/a
7	chr17:45144857-45144907	ECC-1	luminal epithelium:	n/a
8	chr17:45143871-45143921	HUVEC	blood vessel:	n/a
9	chr17:45143871-45143921	MCF10A-Er-Src	breast:	n/a
10	chr17:45144857-45144907	HCM	heart:	n/a
11	chr17:45143871-45143921	NB4	blood:	n/a
12	chr17:45144857-45144907	HNPCEpiC	eye:	n/a
13	chr17:45144857-45144907	MCF10A-Er-Src	breast:	n/a
14	chr17:45143871-45143921	AG09309	skin:	n/a
15	chr17:45143871-45143921	HAEpiC	amniotic membrane:	n/a
16	chr17:45143871-45143921	NH-A	brain:	n/a
17	chr17:45143871-45143921	SK-N-MC	brain:	n/a
18	chr17:45143871-45143921	ovcar-3	ovarian:	n/a
19	chr17:45143871-45143921	GM12878	blood:	n/a
20	chr17:45143871-45143921	AoSMC	blood vessel:	n/a
21	chr17:45144857-45144907	HEK293	kidney:	embryo
22	chr17:45143871-45143921	GM06990	blood:	n/a
23	chr17:45144857-45144907	AG10803	skin:	n/a
24	chr17:45143871-45143921	SK-N-SH	brain:	n/a
25	chr17:45144857-45144907	Caco-2	colon:	n/a
26	chr17:45144857-45144907	AG04449	skin:	fetal
27	chr17:45144857-45144907	Jurkat	blood:	n/a
28	chr17:45144857-45144907	PANC-1	pancreas:	n/a
29	chr17:45143871-45143921	AG10803	skin:	n/a
30	chr17:45143871-45143921	LNCaP	prostate:	n/a
31	chr17:45143871-45143921	GM19239	blood:	n/a
32	chr17:45143871-45143921	Hela-S3	cervix:	n/a
33	chr17:45144857-45144907	Hela-S3	cervix:	n/a
34	chr17:45144857-45144907	HIPEpiC	eye:	n/a
35	chr17:45144857-45144907	HPAEpiC	pulmonary alveolar:	n/a
36	chr17:45143871-45143921	HMEC	breast:	n/a
37	chr17:45144857-45144907	K562	blood:	n/a
38	chr17:45144857-45144907	HMEC	breast:	n/a
39	chr17:45143871-45143921	U87	brain:	n/a
40	chr17:45144857-45144907	A549	lung:	n/a
41	chr17:45143871-45143921	AG04449	skin:	fetal
42	chr17:45143871-45143921	GM12891	blood:	n/a
43	chr17:45143871-45143921	SKMC	muscle:	n/a
44	chr17:45143871-45143921	H1-hESC	embryonic stem cell:	embryo
45	chr17:45143871-45143921	ProgFib	skin:	n/a
46	chr17:45144857-45144907	ovcar-3	ovarian:	n/a
47	chr17:45143871-45143921	SAEC	small airway:	n/a
48	chr17:45144857-45144907	NT2-D1	testis:	n/a
49	chr17:45143871-45143921	Hepatocyte	liver:	n/a
50	chr17:45144857-45144907	HRPEpiC	eye:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:45143352..45146051-chr17:45399301..45401762,3	K562	blood:
2	chr17:45144506..45145240-chr9:130213283..130213833,2	Hela-S3	cervix:
3	chr17:45143352..45144907-chr17:45399301..45401186,2	K562	blood:
4	chr1:28655193..28655793-chr17:45144387..45145240,2	Hela-S3	cervix:
5	chr17:45142727..45145152-chr17:45150394..45151973,2	K562	blood:
6	chr17:45145658..45148463-chr17:45161187..45163786,2	MCF-7	breast:
7	chr17:45148479..45151206-chr17:45175479..45177922,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RPRML-3	chr17:45149838-45149925	ENSG00000262879.1
2	lnc-RPRML-3	chr17:45149723-45149925	NONHSAT054278
3	lnc-RPRML-3	chr17:45149838-45149925	NONHSAT054277
4	lnc-RPRML-3	chr17:45148881-45148978	NONHSAT054277

No data

Variant related genes	Relation type
ENSG00000262879	TF binding region
ENSG00000262879	CpG island
ENSG00000148356	chromatin interactions
ENSG00000262879	chromatin interactions
ENSG00000178852	chromatin interactions
ENSG00000130772	chromatin interactions
ENSG00000197958	chromatin interactions
ENSG00000263293	chromatin interactions

Extended variants
information (count: 360 )
Associated
traits (count: 119 )

Variant overlapped rSNPs/rCNVs (count:360 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs557449667	chr17:45142891-45142892	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs543197849	chr17:45142928-45142929	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs577750950	chr17:45142948-45142949	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs540490748	chr17:45142953-45142954	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs143067954	chr17:45142967-45142968	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs529068441	chr17:45142986-45142987	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs112139365	chr17:45143012-45143013	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs62073856	chr17:45143031-45143032	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs151178260	chr17:45143078-45143079	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs531689580	chr17:45143093-45143094	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs551897693	chr17:45143097-45143098	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs571298694	chr17:45143180-45143181	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs532011081	chr17:45143182-45143183	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs189527002	chr17:45143196-45143197	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs547637358	chr17:45143225-45143226	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs567641206	chr17:45143237-45143238	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs536415704	chr17:45143396-45143397	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs370413188	chr17:45143406-45143407	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs150228833	chr17:45143408-45143409	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs376816250	chr17:45143411-45143412	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs9911627	chr17:45143465-45143466	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs532932061	chr17:45143503-45143504	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs570260637	chr17:45143534-45143535	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs537543000	chr17:45143538-45143539	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs535921712	chr17:45143633-45143634	Enhancers ZNF genes & repeats Weak transcription Active TSS Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs9891199	chr17:45143642-45143643	Enhancers ZNF genes & repeats Weak transcription Active TSS Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs12453392	chr17:45143646-45143647	Enhancers ZNF genes & repeats Weak transcription Active TSS Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs146923264	chr17:45143657-45143658	Enhancers ZNF genes & repeats Weak transcription Active TSS Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs554072445	chr17:45143698-45143699	Enhancers ZNF genes & repeats Weak transcription Active TSS Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs573250937	chr17:45143712-45143713	Enhancers ZNF genes & repeats Weak transcription Active TSS Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs534320822	chr17:45143724-45143725	Enhancers ZNF genes & repeats Weak transcription Active TSS Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs555912094	chr17:45143725-45143726	Enhancers ZNF genes & repeats Weak transcription Active TSS Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs114022269	chr17:45143727-45143728	Enhancers ZNF genes & repeats Weak transcription Active TSS Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs117707904	chr17:45143758-45143759	Enhancers ZNF genes & repeats Weak transcription Active TSS Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs36098545	chr17:45143773-45143774	Enhancers ZNF genes & repeats Weak transcription Active TSS Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs533757433	chr17:45143828-45143829	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs565042882	chr17:45143845-45143846	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs143271878	chr17:45143877-45143878	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs547403564	chr17:45143891-45143892	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs112960692	chr17:45143908-45143909	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs193003095	chr17:45143923-45143924	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs200606460	chr17:45144030-45144031	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs201836561	chr17:45144031-45144032	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs373294483	chr17:45144034-45144035	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs530310446	chr17:45144079-45144080	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs550499188	chr17:45144099-45144100	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs184225202	chr17:45144299-45144300	Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs79917694	chr17:45144306-45144307	Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs539224793	chr17:45144345-45144346	Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs189592292	chr17:45144367-45144368	Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:119)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Melanoma	18172304	CNVD
Moyamoya disease	22323933	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ovarian cancer	21781307	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell lymphomas	19863542	CNVD
Cancer	16751803	CNVD
Chordoma	21602918	CNVD
Neurofibromatosis	20686819	CNVD
Peripheral nerve sheath tumors	20686819	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	17897457	CNVD
Neuroblastoma	17327916	CNVD
Breast cancer	21264507	CNVD
Endometrial cancer	22040021	CNVD
Neuroblastoma	21484798	CNVD
Breast cancer	22028636	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute myeloid leukemia	20724749	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Gastric cancer	17167181	CNVD
Breast cancer	19287154	CNVD
Leukemia	20874852	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Neuroblastoma	18664255	CNVD
Neuroblastoma	17533364	CNVD
Human rectal carcinomas	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Breast cancer	17457667	CNVD
Breast cancer	16951389	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22048815	CNVD
Breast cancer	17603634	CNVD
Follicular lymphoma	20505157	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	20953835	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
TAR Syndrome	17847015	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17850661	CNVD
Breast cancer	19261255	CNVD
Lung cancer	16773561	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Basal-like breast cancer	18066063	CNVD
Breast cancer	20031965	CNVD
Colorectal cancer	19287155	CNVD
Hereditary breast	19566914	CNVD
Ovarian cancer	19047089	CNVD
Ovarian cancer	19566914	CNVD
Triple-negative breast cancer	18950515	CNVD
Breast cancer	16846527	CNVD
Bladder cancer	21909424	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	21251322	CNVD
Ewing''s sarcoma	22429812	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21509527	CNVD
Urothelial carcinoma	21177765	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Breast cancer	17142309	CNVD
Breast cancer	16397240	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Non-syndromic sensorineural hearing loss	21084979	CNVD
Autism	22817714	CNVD
Breast cancer	20409316	CNVD
Cancer	17160897	CNVD
Frontotemporal lobar degeneration	19640594	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:700 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:45123800-45143600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr17:45125200-45143600	Weak transcription	HepG2	liver
3	chr17:45125400-45143800	Weak transcription	NHLF	lung
4	chr17:45128200-45143600	Weak transcription	HSMMtube	muscle
5	chr17:45128200-45143800	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr17:45128800-45143600	Weak transcription	HUVEC	blood vessel
7	chr17:45128800-45144600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr17:45129400-45144200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
9	chr17:45129800-45144000	Weak transcription	Hela-S3	cervix
10	chr17:45130000-45144200	Weak transcription	Primary B cells from cord blood	blood
11	chr17:45130600-45143800	Weak transcription	NHEK	skin
12	chr17:45131200-45143600	Weak transcription	Rectal Smooth Muscle	rectum
13	chr17:45131200-45144000	Weak transcription	Brain Germinal Matrix	brain
14	chr17:45131600-45143600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
15	chr17:45131800-45143600	Weak transcription	HSMM	muscle
16	chr17:45131800-45144600	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr17:45132000-45144600	Weak transcription	Spleen	Spleen
18	chr17:45132200-45143600	Weak transcription	Psoas Muscle	Psoas
19	chr17:45132600-45143600	Weak transcription	Pancreatic Islets	Pancreatic Islet
20	chr17:45132600-45143600	Weak transcription	Osteobl	bone
21	chr17:45132600-45143800	Weak transcription	Brain Cingulate Gyrus	brain
22	chr17:45132600-45144000	Weak transcription	HMEC	breast
23	chr17:45132600-45144200	Weak transcription	Colonic Mucosa	Colon
24	chr17:45133600-45144200	Weak transcription	Fetal Brain Female	brain
25	chr17:45133800-45143400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr17:45133800-45143600	Weak transcription	Primary T cells from cord blood	blood
27	chr17:45133800-45143600	Weak transcription	Primary T cells fromperipheralblood	blood
28	chr17:45133800-45143600	Weak transcription	Brain Substantia Nigra	brain
29	chr17:45133800-45144000	Weak transcription	Cortex derived primary cultured neurospheres	brain
30	chr17:45133800-45144000	Weak transcription	Colon Smooth Muscle	Colon
31	chr17:45133800-45144200	Weak transcription	Primary T helper cells PMA-I stimulated	--
32	chr17:45133800-45144200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
33	chr17:45133800-45144200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
34	chr17:45133800-45144200	Weak transcription	Esophagus	oesophagus
35	chr17:45133800-45144200	Weak transcription	Placenta Amnion	Placenta Amnion
36	chr17:45134000-45143600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
37	chr17:45134000-45143600	Weak transcription	Primary T helper cells fromperipheralblood	blood
38	chr17:45134000-45143600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
39	chr17:45134000-45143600	Weak transcription	Brain Angular Gyrus	brain
40	chr17:45134000-45143600	Weak transcription	Brain Anterior Caudate	brain
41	chr17:45134000-45143600	Weak transcription	Duodenum Mucosa	Duodenum
42	chr17:45134000-45143600	Weak transcription	Duodenum Smooth Muscle	Duodenum
43	chr17:45134000-45143600	Weak transcription	Fetal Kidney	kidney
44	chr17:45134000-45143600	Weak transcription	Pancreas	Pancrea
45	chr17:45134000-45143600	Weak transcription	Skeletal Muscle Male	skeletal muscle
46	chr17:45134000-45143600	Weak transcription	Stomach Mucosa	stomach
47	chr17:45134000-45143600	Weak transcription	GM12878-XiMat	blood
48	chr17:45134000-45143800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr17:45134000-45143800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
50	chr17:45134000-45143800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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