Variant report

Variant	nsv466074
Chromosome Location	chr9:2032845-2074070
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:570)
CpG islands
(count:366)
Chromatin interactive
region (count:22)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:570 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr9:2055011-2055808	GM12878	blood:	n/a	n/a
2	ATF2	chr9:2053653-2054478	GM12878	blood:	n/a	n/a
3	ATF2	chr9:2043092-2043667	GM12878	blood:	n/a	n/a
4	ATF2	chr9:2053700-2054321	GM12878	blood:	n/a	n/a
5	ATF2	chr9:2043068-2043725	GM12878	blood:	n/a	n/a
6	ATF2	chr9:2054946-2055805	GM12878	blood:	n/a	n/a
7	BATF	chr9:2055078-2055684	GM12878	blood:	n/a	chr9:2055534-2055544
8	BATF	chr9:2043195-2043566	GM12878	blood:	n/a	n/a
9	BATF	chr9:2053830-2054274	GM12878	blood:	n/a	n/a
10	BATF	chr9:2055036-2055733	GM12878	blood:	n/a	chr9:2055534-2055544
11	BATF	chr9:2066304-2066596	GM12878	blood:	n/a	n/a
12	BATF	chr9:2043270-2043543	GM12878	blood:	n/a	n/a
13	BCL11A	chr9:2053866-2054307	GM12878	blood:	n/a	n/a
14	BCL11A	chr9:2055123-2055702	GM12878	blood:	n/a	n/a
15	BCL11A	chr9:2059398-2059873	GM12878	blood:	n/a	n/a
16	BCL11A	chr9:2055057-2055743	GM12878	blood:	n/a	n/a
17	BCL11A	chr9:2053878-2054277	GM12878	blood:	n/a	n/a
18	BCL3	chr9:2055084-2055684	GM12878	blood:	n/a	n/a
19	BCL3	chr9:2053747-2054301	GM12878	blood:	n/a	n/a
20	BCLAF1	chr9:2043986-2044753	GM12878	blood:	n/a	n/a
21	BCLAF1	chr9:2043238-2043879	GM12878	blood:	n/a	chr9:2043484-2043493
22	BCLAF1	chr9:2053773-2054316	GM12878	blood:	n/a	n/a
23	BCLAF1	chr9:2053364-2054381	GM12878	blood:	n/a	n/a
24	BCLAF1	chr9:2055206-2055756	GM12878	blood:	n/a	n/a
25	BHLHE40	chr9:2069977-2070015	HepG2	liver:	n/a	n/a
26	BHLHE40	chr9:2053738-2054542	GM12878	blood:	n/a	n/a
27	CEBPB	chr9:2055286-2055624	IMR90	lung:	n/a	n/a
28	CEBPB	chr9:2051511-2051590	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr9:2053906-2054237	GM12878	blood:	n/a	n/a
30	CEBPB	chr9:2067430-2067645	A549	lung:	n/a	n/a
31	CEBPB	chr9:2054991-2055898	GM12878	blood:	n/a	n/a
32	CEBPB	chr9:2067495-2067627	IMR90	lung:	n/a	n/a
33	CEBPB	chr9:2067380-2067661	HepG2	liver:	n/a	n/a
34	CHD2	chr9:2053800-2054488	GM12878	blood:	n/a	n/a
35	CREB1	chr9:2053767-2054383	GM12878	blood:	n/a	n/a
36	CREB1	chr9:2053718-2054421	GM12878	blood:	n/a	n/a
37	CTCF	chr9:2067020-2067170	BJ	skin:	n/a	n/a
38	CTCF	chr9:2067000-2067150	AG09319	gingival:	n/a	n/a
39	CTCF	chr9:2067080-2067230	HAc	cerebellar:	n/a	n/a
40	CTCF	chr9:2066920-2067070	HMEC	breast:	n/a	n/a
41	CTCF	chr9:2067000-2067162	K562	blood:	n/a	n/a
42	CTCF	chr9:2059640-2059840	GM12878	blood:	n/a	n/a
43	CTCF	chr9:2067020-2067170	GM12873	blood:	n/a	n/a
44	CTCF	chr9:2067050-2067111	GM13977	blood:	n/a	n/a
45	CTCF	chr9:2067060-2067210	HBMEC	blood vessel:	n/a	n/a
46	CTCF	chr9:2066843-2067201	MCF-7	breast:	n/a	n/a
47	CTCF	chr9:2066880-2067030	WI-38	lung:	n/a	n/a
48	CTCF	chr9:2066960-2067110	AoAF	blood vessel:	n/a	n/a
49	CTCF	chr9:2067020-2067170	GM12864	blood:	n/a	n/a
50	CTCF	chr9:2066980-2067130	HCPEpiC	choroid plexus:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:2047160-2047210	HEK293	kidney:	embryo
2	chr9:2044055-2044105	HAEpiC	amniotic membrane:	n/a
3	chr9:2047595-2047645	RPTEC	kidney:	n/a
4	chr9:2044055-2044105	HIPEpiC	eye:	n/a
5	chr9:2044055-2044105	SK-N-SH_RA	brain:	n/a
6	chr9:2050899-2050949	GM12892	blood:	n/a
7	chr9:2050899-2050949	PrEC	prostate:	n/a
8	chr9:2047373-2047423	Jurkat	blood:	n/a
9	chr9:2047373-2047423	PFSK-1	brain:	n/a
10	chr9:2047595-2047645	GM12892	blood:	n/a
11	chr9:2044055-2044105	HCPEpiC	choroid plexus:	n/a
12	chr9:2047595-2047645	Caco-2	colon:	n/a
13	chr9:2050899-2050949	HL-60	blood:	n/a
14	chr9:2047160-2047210	SK-N-MC	brain:	n/a
15	chr9:2044055-2044105	BE2_C	brain:	n/a
16	chr9:2047373-2047423	NHBE	bronchial:	n/a
17	chr9:2044055-2044105	HL-60	blood:	n/a
18	chr9:2047373-2047423	Hepatocyte	liver:	n/a
19	chr9:2047160-2047210	MCF-7	breast:	n/a
20	chr9:2047800-2047850	GM12892	blood:	n/a
21	chr9:2047160-2047210	GM06990	blood:	n/a
22	chr9:2047595-2047645	ProgFib	skin:	n/a
23	chr9:2047160-2047210	GM12878	blood:	n/a
24	chr9:2047800-2047850	K562	blood:	n/a
25	chr9:2044055-2044105	NH-A	brain:	n/a
26	chr9:2047160-2047210	NHBE	bronchial:	n/a
27	chr9:2047373-2047423	PrEC	prostate:	n/a
28	chr9:2047595-2047645	AG09319	gingival:	n/a
29	chr9:2047800-2047850	GM06990	blood:	n/a
30	chr9:2047160-2047210	HCF	heart:	n/a
31	chr9:2050899-2050949	HAEpiC	amniotic membrane:	n/a
32	chr9:2044055-2044105	MCF10A-Er-Src	breast:	n/a
33	chr9:2047800-2047850	AG09319	gingival:	n/a
34	chr9:2047800-2047850	HCF	heart:	n/a
35	chr9:2047160-2047210	HCT-116	colon:	n/a
36	chr9:2050899-2050949	HepG2	liver:	n/a
37	chr9:2047373-2047423	MCF10A-Er-Src	breast:	n/a
38	chr9:2050899-2050949	GM06990	blood:	n/a
39	chr9:2047800-2047850	MCF10A-Er-Src	breast:	n/a
40	chr9:2047800-2047850	HepG2	liver:	n/a
41	chr9:2050899-2050949	SK-N-SH	brain:	n/a
42	chr9:2050899-2050949	Caco-2	colon:	n/a
43	chr9:2047800-2047850	SAEC	small airway:	n/a
44	chr9:2047595-2047645	HEEpiC	esophagus:	n/a
45	chr9:2047160-2047210	NB4	blood:	n/a
46	chr9:2047160-2047210	K562	blood:	n/a
47	chr9:2050899-2050949	Hela-S3	cervix:	n/a
48	chr9:2047373-2047423	AG10803	skin:	n/a
49	chr9:2044055-2044105	HRPEpiC	eye:	n/a
50	chr9:2047800-2047850	ovcar-3	ovarian:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:2038457..2040329-chr9:2040850..2042831,2	K562	blood:
2	chr9:2012580..2014743-chr9:2038420..2041072,2	K562	blood:
3	chr9:2016166..2018399-chr9:2051368..2053339,2	MCF-7	breast:
4	chr9:2027773..2030143-chr9:2034628..2037514,2	K562	blood:
5	chr9:2027542..2030484-chr9:2031269..2033941,3	K562	blood:
6	chr9:2061237..2063006-chr9:2063719..2066539,2	K562	blood:
7	chr9:2016948..2019401-chr9:2068781..2070385,2	MCF-7	breast:
8	chr9:2038457..2040329-chr9:2040850..2042831,2	K562	blood:
9	chr9:2031596..2033809-chr9:2036447..2038109,2	MCF-7	breast:
10	chr9:2035867..2037863-chr9:2040595..2043579,2	MCF-7	breast:
11	chr9:2015277..2016837-chr9:2046158..2048018,2	K562	blood:
12	chr9:2014062..2016473-chr9:2041837..2045472,3	MCF-7	breast:
13	chr9:2014489..2016511-chr9:2066212..2068333,2	MCF-7	breast:
14	chr9:2016568..2019114-chr9:2030660..2033552,2	MCF-7	breast:
15	chr9:2035867..2037863-chr9:2040595..2043579,2	MCF-7	breast:
16	chr9:2014709..2017122-chr9:2062966..2067398,3	MCF-7	breast:
17	chr9:2015290..2017230-chr9:2035454..2037354,2	MCF-7	breast:
18	chr9:2030993..2033791-chr9:2034490..2037168,2	K562	blood:
19	chr9:2015330..2018297-chr9:2035684..2039047,3	MCF-7	breast:
20	chr9:2061237..2063006-chr9:2063719..2066539,2	K562	blood:
21	chr9:2025406..2027101-chr9:2041465..2044182,2	K562	blood:
22	chr9:2035810..2037705-chr9:2044015..2046964,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KIAA0020-2	chr9:2041900-2042130	ENSG00000236199.1
2	lnc-KIAA0020-2	chr9:2045835-2046023	ENSG00000236199.1
3	lnc-VLDLR-4	chr9:2042994-2046019	NONHSAT129986

No data

Variant related genes	Relation type
ENSG00000236199	TF binding region
ENSG00000236199	CpG island
ENSG00000080503	chromatin interactions
ENSG00000236199	chromatin interactions

Extended variants
information (count: 1969 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:1969 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1112534	chr9:2032845-2032846	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs568138151	chr9:2032877-2032878	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs537275074	chr9:2032889-2032890	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs557073252	chr9:2032897-2032898	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs377532438	chr9:2032900-2032901	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs373127967	chr9:2032923-2032924	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs149279147	chr9:2032932-2032933	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs148086416	chr9:2032957-2032958	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs201962378	chr9:2032968-2032969	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs141861118	chr9:2032970-2032971	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs181403075	chr9:2032972-2032973	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs370078162	chr9:2032990-2032991	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs564889539	chr9:2033038-2033039	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs533959336	chr9:2033046-2033047	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs150630640	chr9:2033050-2033051	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs374114848	chr9:2033051-2033052	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs368021380	chr9:2033084-2033085	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs376665212	chr9:2033091-2033092	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs370152390	chr9:2033120-2033121	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs370288630	chr9:2033130-2033131	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs550732830	chr9:2033153-2033154	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs1112533	chr9:2033182-2033183	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs533228509	chr9:2033191-2033192	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs144428938	chr9:2033227-2033228	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs566746931	chr9:2033274-2033275	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs186542538	chr9:2033326-2033327	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs369195546	chr9:2033341-2033342	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs548170577	chr9:2033404-2033405	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs539452237	chr9:2033449-2033450	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs117779686	chr9:2033453-2033454	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs148407615	chr9:2033472-2033473	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs375424689	chr9:2033533-2033534	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs143021439	chr9:2033534-2033535	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs539114909	chr9:2033563-2033564	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs370234170	chr9:2033642-2033643	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs77381160	chr9:2033657-2033658	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs10811337	chr9:2033745-2033746	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs113605155	chr9:2033763-2033764	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs190719032	chr9:2033785-2033786	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs575497444	chr9:2033855-2033856	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs140200865	chr9:2033869-2033870	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs74390427	chr9:2033895-2033896	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs564293180	chr9:2033904-2033905	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs533619697	chr9:2033905-2033906	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs10964497	chr9:2033929-2033930	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs560667828	chr9:2034017-2034018	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs572576820	chr9:2034018-2034019	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs529248686	chr9:2034020-2034021	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs551681130	chr9:2034073-2034074	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs541582669	chr9:2034105-2034106	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:109)

Disease	PMID	Source
Myelofibrosis	22110671	CNVD
Lynch syndrome	18415027	CNVD
Retinoblastoma	21504564	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	22286061	CNVD
Williams-beuren syndrome	18553513	CNVD
Disorders of sex development	21048976	CNVD
Pilocytic astrocytoma	18622384	CNVD
Pilomyxoid astrocytoma	18622384	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
prenatal diagnosis	20453657	CNVD
Gastric cancer	16715143	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Intracranial aneurysm	16715129	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Disorders of sex development	22290220	CNVD
Glioblastoma multiforme	21080181	CNVD
Sudden cardiac death	19188705	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	21952639	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
abnormal development	18461090	CNVD
Honadal dysgenesis	21048976	CNVD
Medulloblastoma	21979893	CNVD
Lung cancer	16740712	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Autism	20531469	CNVD
XY gonadal dysgenesis	20685758	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1565 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:2018200-2033400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr9:2019000-2033200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr9:2019200-2039400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr9:2019400-2033000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr9:2019400-2033200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr9:2020000-2033000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr9:2023600-2033000	Weak transcription	Fetal Brain Female	brain
8	chr9:2024000-2039400	Weak transcription	Stomach Mucosa	stomach
9	chr9:2025000-2033000	Weak transcription	HSMMtube	muscle
10	chr9:2025200-2033000	Weak transcription	Thymus	Thymus
11	chr9:2025200-2044600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
12	chr9:2025400-2033000	Weak transcription	Colonic Mucosa	Colon
13	chr9:2025400-2044000	Weak transcription	HUES48 Cell Line	embryonic stem cell
14	chr9:2025600-2033000	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr9:2025600-2033000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr9:2025600-2040000	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr9:2025600-2041200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr9:2025800-2033000	Weak transcription	Fetal Thymus	thymus
19	chr9:2025800-2033000	Weak transcription	HepG2	liver
20	chr9:2025800-2043600	Weak transcription	Fetal Heart	heart
21	chr9:2026000-2033000	Weak transcription	Fetal Intestine Small	intestine
22	chr9:2026000-2037400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr9:2026000-2047400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr9:2026200-2033000	Weak transcription	Aorta	Aorta
25	chr9:2028000-2033000	Weak transcription	Gastric	stomach
26	chr9:2028000-2040000	Weak transcription	HMEC	breast
27	chr9:2028200-2033000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr9:2028200-2033000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr9:2028200-2033000	Weak transcription	Right Ventricle	heart
30	chr9:2028200-2033400	Weak transcription	Esophagus	oesophagus
31	chr9:2028400-2033000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
32	chr9:2028400-2033200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr9:2028600-2033200	Enhancers	Pancreatic Islets	Pancreatic Islet
34	chr9:2029000-2125200	Strong transcription	Monocytes-CD14+_RO01746	blood
35	chr9:2029200-2033000	Weak transcription	Brain Angular Gyrus	brain
36	chr9:2029200-2033000	Weak transcription	Placenta	Placenta
37	chr9:2029200-2033000	Weak transcription	Pancreas	Pancrea
38	chr9:2029200-2033000	Weak transcription	Placenta Amnion	Placenta Amnion
39	chr9:2029200-2039600	Weak transcription	Psoas Muscle	Psoas
40	chr9:2029200-2042600	Strong transcription	Primary B cells from peripheral blood	blood
41	chr9:2029200-2053000	Weak transcription	Small Intestine	intestine
42	chr9:2029400-2043800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
43	chr9:2029600-2033000	Weak transcription	NHLF	lung
44	chr9:2029600-2033200	Weak transcription	NH-A	brain
45	chr9:2029600-2051800	Strong transcription	Liver	Liver
46	chr9:2030000-2040800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
47	chr9:2030600-2033000	Weak transcription	Duodenum Smooth Muscle	Duodenum
48	chr9:2030600-2033000	Weak transcription	Fetal Stomach	stomach
49	chr9:2030600-2033000	Weak transcription	Lung	lung
50	chr9:2030800-2033000	Weak transcription	HSMM	muscle

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