Variant report

Variant	nsv613086
Chromosome Location	chr9:2034666-2059341
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:366)
CpG islands
(count:366)
Chromatin interactive
region (count:15)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr9:2053700-2054321	GM12878	blood:	n/a	n/a
2	ATF2	chr9:2055011-2055808	GM12878	blood:	n/a	n/a
3	ATF2	chr9:2043092-2043667	GM12878	blood:	n/a	n/a
4	ATF2	chr9:2054946-2055805	GM12878	blood:	n/a	n/a
5	ATF2	chr9:2043068-2043725	GM12878	blood:	n/a	n/a
6	ATF2	chr9:2053653-2054478	GM12878	blood:	n/a	n/a
7	BATF	chr9:2043195-2043566	GM12878	blood:	n/a	n/a
8	BATF	chr9:2055036-2055733	GM12878	blood:	n/a	chr9:2055534-2055544
9	BATF	chr9:2043270-2043543	GM12878	blood:	n/a	n/a
10	BATF	chr9:2053830-2054274	GM12878	blood:	n/a	n/a
11	BATF	chr9:2055078-2055684	GM12878	blood:	n/a	chr9:2055534-2055544
12	BCL11A	chr9:2055057-2055743	GM12878	blood:	n/a	n/a
13	BCL11A	chr9:2053866-2054307	GM12878	blood:	n/a	n/a
14	BCL11A	chr9:2053878-2054277	GM12878	blood:	n/a	n/a
15	BCL11A	chr9:2055123-2055702	GM12878	blood:	n/a	n/a
16	BCL3	chr9:2053747-2054301	GM12878	blood:	n/a	n/a
17	BCL3	chr9:2055084-2055684	GM12878	blood:	n/a	n/a
18	BCLAF1	chr9:2055206-2055756	GM12878	blood:	n/a	n/a
19	BCLAF1	chr9:2053773-2054316	GM12878	blood:	n/a	n/a
20	BCLAF1	chr9:2043238-2043879	GM12878	blood:	n/a	chr9:2043484-2043493
21	BCLAF1	chr9:2043986-2044753	GM12878	blood:	n/a	n/a
22	BCLAF1	chr9:2053364-2054381	GM12878	blood:	n/a	n/a
23	BHLHE40	chr9:2053738-2054542	GM12878	blood:	n/a	n/a
24	CEBPB	chr9:2051511-2051590	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr9:2055286-2055624	IMR90	lung:	n/a	n/a
26	CEBPB	chr9:2054991-2055898	GM12878	blood:	n/a	n/a
27	CEBPB	chr9:2053906-2054237	GM12878	blood:	n/a	n/a
28	CHD2	chr9:2053800-2054488	GM12878	blood:	n/a	n/a
29	CREB1	chr9:2053718-2054421	GM12878	blood:	n/a	n/a
30	CREB1	chr9:2053767-2054383	GM12878	blood:	n/a	n/a
31	CTCF	chr9:2055440-2055590	HMF	breast:	n/a	n/a
32	CTCF	chr9:2044480-2044630	AG09309	skin:	n/a	n/a
33	CTCF	chr9:2053220-2053370	AG09309	skin:	n/a	n/a
34	CUX1	chr9:2053708-2054248	GM12878	blood:	n/a	n/a
35	CUX1	chr9:2043289-2043642	GM12878	blood:	n/a	n/a
36	CUX1	chr9:2055112-2055648	GM12878	blood:	n/a	chr9:2055237-2055253
37	E2F4	chr9:2055400-2055752	MCF10A-Er-Src	breast:	n/a	n/a
38	E2F4	chr9:2050399-2050457	MCF10A-Er-Src	breast:	n/a	n/a
39	EBF1	chr9:2038293-2038642	GM12878	blood:	n/a	chr9:2038464-2038475
40	EBF1	chr9:2038330-2038633	GM12878	blood:	n/a	chr9:2038464-2038475
41	EBF1	chr9:2053849-2054258	GM12878	blood:	n/a	n/a
42	EBF1	chr9:2053878-2054308	GM12878	blood:	n/a	n/a
43	EBF1	chr9:2055088-2055655	GM12878	blood:	n/a	n/a
44	EBF1	chr9:2043274-2043472	GM12878	blood:	n/a	n/a
45	EBF1	chr9:2053807-2054387	GM12878	blood:	n/a	n/a
46	EBF1	chr9:2055260-2055660	GM12878	blood:	n/a	n/a
47	ELF1	chr9:2053786-2054315	GM12878	blood:	n/a	n/a
48	EP300	chr9:2055011-2055790	GM12878	blood:	n/a	chr9:2055033-2055043
49	EP300	chr9:2058701-2060033	SK-N-SH	brain:	n/a	chr9:2059351-2059361
50	EP300	chr9:2043243-2043798	GM12878	blood:	n/a	chr9:2043467-2043481 chr9:2043479-2043493 chr9:2043443-2043457

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:2047373-2047423	ECC-1	luminal epithelium:	n/a
2	chr9:2047800-2047850	SAEC	small airway:	n/a
3	chr9:2050899-2050949	H1-hESC	embryonic stem cell:	embryo
4	chr9:2047373-2047423	NT2-D1	testis:	n/a
5	chr9:2047800-2047850	NT2-D1	testis:	n/a
6	chr9:2047160-2047210	HL-60	blood:	n/a
7	chr9:2047595-2047645	NHDF-neo	bronchial:	n/a
8	chr9:2047800-2047850	CMK	blood:	n/a
9	chr9:2047800-2047850	AG09319	gingival:	n/a
10	chr9:2047595-2047645	GM12891	blood:	n/a
11	chr9:2047595-2047645	HRCEpiC	kidney:	n/a
12	chr9:2047595-2047645	AoSMC	blood vessel:	n/a
13	chr9:2044055-2044105	BJ	skin:	n/a
14	chr9:2047595-2047645	LNCaP	prostate:	n/a
15	chr9:2047595-2047645	HCPEpiC	choroid plexus:	n/a
16	chr9:2047595-2047645	SK-N-MC	brain:	n/a
17	chr9:2044055-2044105	ECC-1	luminal epithelium:	n/a
18	chr9:2047800-2047850	HCM	heart:	n/a
19	chr9:2044055-2044105	GM12878	blood:	n/a
20	chr9:2047373-2047423	HPAEpiC	pulmonary alveolar:	n/a
21	chr9:2047800-2047850	NB4	blood:	n/a
22	chr9:2050899-2050949	HCPEpiC	choroid plexus:	n/a
23	chr9:2050899-2050949	AG04450	lung:	fetal
24	chr9:2044055-2044105	HepG2	liver:	n/a
25	chr9:2047595-2047645	Hela-S3	cervix:	n/a
26	chr9:2050899-2050949	SK-N-MC	brain:	n/a
27	chr9:2047160-2047210	SAEC	small airway:	n/a
28	chr9:2047160-2047210	GM19239	blood:	n/a
29	chr9:2047373-2047423	HEEpiC	esophagus:	n/a
30	chr9:2047800-2047850	HRPEpiC	eye:	n/a
31	chr9:2044055-2044105	HL-60	blood:	n/a
32	chr9:2044055-2044105	AG09319	gingival:	n/a
33	chr9:2050899-2050949	SK-N-SH	brain:	n/a
34	chr9:2047160-2047210	HRPEpiC	eye:	n/a
35	chr9:2047160-2047210	ProgFib	skin:	n/a
36	chr9:2047160-2047210	SK-N-MC	brain:	n/a
37	chr9:2047373-2047423	BJ	skin:	n/a
38	chr9:2047373-2047423	IMR90	lung:	fetal
39	chr9:2047160-2047210	HNPCEpiC	eye:	n/a
40	chr9:2047373-2047423	MCF10A-Er-Src	breast:	n/a
41	chr9:2047373-2047423	HRPEpiC	eye:	n/a
42	chr9:2050899-2050949	SAEC	small airway:	n/a
43	chr9:2050899-2050949	AG09309	skin:	n/a
44	chr9:2050899-2050949	MCF10A-Er-Src	breast:	n/a
45	chr9:2047373-2047423	HUVEC	blood vessel:	n/a
46	chr9:2044055-2044105	CMK	blood:	n/a
47	chr9:2047373-2047423	SK-N-SH	brain:	n/a
48	chr9:2047160-2047210	HCM	heart:	n/a
49	chr9:2047800-2047850	HCPEpiC	choroid plexus:	n/a
50	chr9:2044055-2044105	HUVEC	blood vessel:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:2012580..2014743-chr9:2038420..2041072,2	K562	blood:
2	chr9:2016166..2018399-chr9:2051368..2053339,2	MCF-7	breast:
3	chr9:2035810..2037705-chr9:2044015..2046964,2	K562	blood:
4	chr9:2035867..2037863-chr9:2040595..2043579,2	MCF-7	breast:
5	chr9:2014062..2016473-chr9:2041837..2045472,3	MCF-7	breast:
6	chr9:2031596..2033809-chr9:2036447..2038109,2	MCF-7	breast:
7	chr9:2035867..2037863-chr9:2040595..2043579,2	MCF-7	breast:
8	chr9:2030993..2033791-chr9:2034490..2037168,2	K562	blood:
9	chr9:2015290..2017230-chr9:2035454..2037354,2	MCF-7	breast:
10	chr9:2015330..2018297-chr9:2035684..2039047,3	MCF-7	breast:
11	chr9:2025406..2027101-chr9:2041465..2044182,2	K562	blood:
12	chr9:2027773..2030143-chr9:2034628..2037514,2	K562	blood:
13	chr9:2038457..2040329-chr9:2040850..2042831,2	K562	blood:
14	chr9:2038457..2040329-chr9:2040850..2042831,2	K562	blood:
15	chr9:2015277..2016837-chr9:2046158..2048018,2	K562	blood:

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

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

No data

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

Extended variants
information (count: 1144 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:1144 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10964502	chr9:2034666-2034667	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs568500461	chr9:2034729-2034730	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs191147342	chr9:2034765-2034766	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs558005490	chr9:2034773-2034774	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs547412791	chr9:2034774-2034775	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs540587945	chr9:2034781-2034782	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs182287065	chr9:2034840-2034841	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs574157142	chr9:2034898-2034899	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs7862617	chr9:2034908-2034909	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs563012493	chr9:2034923-2034924	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs576490412	chr9:2034924-2034925	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs3057853	chr9:2035008-2035009	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs555705616	chr9:2035009-2035010	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs567408279	chr9:2035020-2035021	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs57411199	chr9:2035046-2035047	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs545448048	chr9:2035047-2035048	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs67210108	chr9:2035053-2035054	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs10964504	chr9:2035099-2035100	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs556164900	chr9:2035122-2035123	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs7852483	chr9:2035128-2035129	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs201090709	chr9:2035132-2035133	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs546581251	chr9:2035133-2035134	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs560291943	chr9:2035174-2035175	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs374704977	chr9:2035201-2035202	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs188038247	chr9:2035234-2035235	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs371701664	chr9:2035246-2035247	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs373586624	chr9:2035307-2035308	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs535422553	chr9:2035309-2035310	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs191029756	chr9:2035340-2035341	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs537568914	chr9:2035364-2035365	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs551323723	chr9:2035389-2035390	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs571166710	chr9:2035397-2035398	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs376596608	chr9:2035414-2035415	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs534460976	chr9:2035415-2035416	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs183291920	chr9:2035424-2035425	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs574274781	chr9:2035432-2035433	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs536882090	chr9:2035452-2035453	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs529737183	chr9:2035455-2035456	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs35257497	chr9:2035474-2035475	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs556673318	chr9:2035501-2035502	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs576578360	chr9:2035513-2035514	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs114625206	chr9:2035537-2035538	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs565236279	chr9:2035554-2035555	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs555804985	chr9:2035604-2035605	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs188272133	chr9:2035631-2035632	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs116749428	chr9:2035685-2035686	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs192017771	chr9:2035709-2035710	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs572353745	chr9:2035743-2035744	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs3838718	chr9:2035748-2035749	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs369548187	chr9:2035760-2035761	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:108)

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

Chromatin state (count:1121 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:2019200-2039400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr9:2024000-2039400	Weak transcription	Stomach Mucosa	stomach
3	chr9:2025200-2044600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr9:2025400-2044000	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr9:2025600-2040000	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr9:2025600-2041200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr9:2025800-2043600	Weak transcription	Fetal Heart	heart
8	chr9:2026000-2037400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr9:2026000-2047400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr9:2028000-2040000	Weak transcription	HMEC	breast
11	chr9:2029000-2125200	Strong transcription	Monocytes-CD14+_RO01746	blood
12	chr9:2029200-2039600	Weak transcription	Psoas Muscle	Psoas
13	chr9:2029200-2042600	Strong transcription	Primary B cells from peripheral blood	blood
14	chr9:2029200-2053000	Weak transcription	Small Intestine	intestine
15	chr9:2029400-2043800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
16	chr9:2029600-2051800	Strong transcription	Liver	Liver
17	chr9:2030000-2040800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
18	chr9:2031400-2048400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
19	chr9:2031400-2052200	Strong transcription	Primary monocytes fromperipheralblood	blood
20	chr9:2031600-2035000	Strong transcription	HUVEC	blood vessel
21	chr9:2031600-2039600	Strong transcription	GM12878-XiMat	blood
22	chr9:2031800-2035000	Strong transcription	Primary T cells from cord blood	blood
23	chr9:2031800-2043600	Strong transcription	Primary T helper cells fromperipheralblood	blood
24	chr9:2031800-2043800	Strong transcription	Primary T cells fromperipheralblood	blood
25	chr9:2032000-2035200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr9:2032000-2044200	Strong transcription	Dnd41	blood
27	chr9:2032200-2035000	Strong transcription	Rectal Mucosa Donor 29	rectum
28	chr9:2032200-2035200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
29	chr9:2032200-2036200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr9:2032200-2042400	Strong transcription	Primary B cells from cord blood	blood
31	chr9:2032200-2044200	Strong transcription	Rectal Mucosa Donor 31	rectum
32	chr9:2032400-2034800	Strong transcription	Cortex derived primary cultured neurospheres	brain
33	chr9:2032400-2034800	Strong transcription	Duodenum Mucosa	Duodenum
34	chr9:2032400-2034800	Strong transcription	Fetal Muscle Leg	muscle
35	chr9:2032400-2034800	Strong transcription	Stomach Smooth Muscle	stomach
36	chr9:2032400-2034800	Strong transcription	Hela-S3	cervix
37	chr9:2032400-2035000	Strong transcription	Fetal Intestine Large	intestine
38	chr9:2032400-2035400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
39	chr9:2032400-2035600	Strong transcription	Primary T killer naive cells fromperipheralblood	blood
40	chr9:2032400-2035600	Strong transcription	Brain Inferior Temporal Lobe	brain
41	chr9:2032400-2035600	Strong transcription	Fetal Muscle Trunk	muscle
42	chr9:2032400-2039400	Weak transcription	Right Atrium	heart
43	chr9:2032400-2040800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
44	chr9:2032400-2045000	Strong transcription	Primary neutrophils fromperipheralblood	blood
45	chr9:2032600-2034800	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
46	chr9:2032600-2034800	Strong transcription	Brain Cingulate Gyrus	brain
47	chr9:2032600-2034800	Strong transcription	Skeletal Muscle Female	skeletal muscle
48	chr9:2032600-2034800	Strong transcription	A549	lung
49	chr9:2032600-2035000	Strong transcription	Muscle Satellite Cultured Cells	--
50	chr9:2032600-2035000	Strong transcription	Fetal Lung	lung

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