Variant report

Variant	nsv1014990
Chromosome Location	chr1:92084142-92206674
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1313)
CpG islands
(count:1038)
Chromatin interactive
region (count:105)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:8)

(count:1313 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:92202453-92203118	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:92163141-92163300	K562	blood:	n/a	n/a
3	ARID3A	chr1:92196941-92197327	K562	blood:	n/a	chr1:92197183-92197199
4	ARID3A	chr1:92171705-92172336	K562	blood:	n/a	n/a
5	ARID3A	chr1:92191604-92191892	HepG2	liver:	n/a	n/a
6	ARID3A	chr1:92190309-92190531	K562	blood:	n/a	n/a
7	ARID3A	chr1:92181905-92182533	K562	blood:	n/a	n/a
8	ARID3A	chr1:92197761-92198425	K562	blood:	n/a	n/a
9	ATF1	chr1:92196313-92196636	K562	blood:	n/a	n/a
10	ATF1	chr1:92181927-92182317	K562	blood:	n/a	n/a
11	ATF1	chr1:92178624-92179281	K562	blood:	n/a	n/a
12	ATF1	chr1:92171779-92172334	K562	blood:	n/a	n/a
13	ATF1	chr1:92197884-92198458	K562	blood:	n/a	n/a
14	ATF2	chr1:92110452-92110814	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr1:92178671-92179395	GM12878	blood:	n/a	n/a
16	ATF3	chr1:92196237-92196599	K562	blood:	n/a	n/a
17	ATF3	chr1:92197931-92198501	K562	blood:	n/a	n/a
18	ATF3	chr1:92198028-92198372	K562	blood:	n/a	n/a
19	BACH1	chr1:92197491-92198200	K562	blood:	n/a	n/a
20	BACH1	chr1:92183826-92183910	K562	blood:	n/a	n/a
21	BACH1	chr1:92179079-92179250	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr1:92172316-92172596	K562	blood:	n/a	n/a
23	BATF	chr1:92162955-92163389	GM12878	blood:	n/a	n/a
24	BATF	chr1:92178946-92179304	GM12878	blood:	n/a	n/a
25	BATF	chr1:92162962-92163345	GM12878	blood:	n/a	n/a
26	BCL3	chr1:92197385-92197844	A549	lung:	n/a	chr1:92197586-92197595
27	BCL3	chr1:92197434-92197789	A549	lung:	n/a	chr1:92197586-92197595
28	BCL3	chr1:92197333-92197701	GM12878	blood:	n/a	chr1:92197586-92197595
29	BCLAF1	chr1:92175696-92176195	GM12878	blood:	n/a	n/a
30	BCLAF1	chr1:92178690-92179438	GM12878	blood:	n/a	chr1:92179162-92179171 chr1:92179161-92179170
31	BHLHE40	chr1:92202481-92202959	HepG2	liver:	n/a	n/a
32	BHLHE40	chr1:92181837-92182347	K562	blood:	n/a	n/a
33	BHLHE40	chr1:92202555-92202860	A549	lung:	n/a	n/a
34	BHLHE40	chr1:92178632-92179229	K562	blood:	n/a	n/a
35	BHLHE40	chr1:92179668-92179800	GM12878	blood:	n/a	chr1:92179708-92179721
36	BHLHE40	chr1:92117159-92117406	K562	blood:	n/a	n/a
37	BHLHE40	chr1:92196306-92198601	K562	blood:	n/a	n/a
38	BHLHE40	chr1:92191192-92191235	K562	blood:	n/a	n/a
39	BHLHE40	chr1:92180324-92181000	K562	blood:	n/a	n/a
40	BHLHE40	chr1:92171698-92172130	K562	blood:	n/a	n/a
41	BHLHE40	chr1:92195148-92195280	K562	blood:	n/a	n/a
42	BRCA1	chr1:92202431-92202939	Hela-S3	cervix:	n/a	n/a
43	BRCA1	chr1:92200064-92200100	GM12878	blood:	n/a	n/a
44	CBX3	chr1:92197685-92198551	K562	blood:	n/a	n/a
45	CBX3	chr1:92196661-92197390	K562	blood:	n/a	n/a
46	CBX3	chr1:92124560-92124878	K562	blood:	n/a	n/a
47	CBX3	chr1:92197993-92198468	K562	blood:	n/a	n/a
48	CBX3	chr1:92171537-92172394	K562	blood:	n/a	n/a
49	CBX3	chr1:92178523-92179430	K562	blood:	n/a	n/a
50	CBX3	chr1:92121412-92122078	K562	blood:	n/a	n/a

(count:1038 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:92117004-92117054	PrEC	prostate:	n/a
2	chr1:92117004-92117054	PrEC	prostate:	n/a
3	chr1:92197531-92197581	ECC-1	luminal epithelium:	n/a
4	chr1:92191625-92191675	SK-N-SH	brain:	n/a
5	chr1:92102055-92102105	BJ	skin:	n/a
6	chr1:92179761-92179811	HNPCEpiC	eye:	n/a
7	chr1:92150549-92150599	AG04450	lung:	fetal
8	chr1:92149139-92149189	GM12878	blood:	n/a
9	chr1:92135648-92135698	NB4	blood:	n/a
10	chr1:92102055-92102105	HRPEpiC	eye:	n/a
11	chr1:92101219-92101269	Hepatocyte	liver:	n/a
12	chr1:92100082-92100132	A549	lung:	n/a
13	chr1:92102055-92102105	NHBE	bronchial:	n/a
14	chr1:92117004-92117054	NHDF-neo	bronchial:	n/a
15	chr1:92150549-92150599	HEK293	kidney:	embryo
16	chr1:92150549-92150599	GM12878	blood:	n/a
17	chr1:92149139-92149189	Caco-2	colon:	n/a
18	chr1:92117004-92117054	GM12891	blood:	n/a
19	chr1:92099528-92099578	HNPCEpiC	eye:	n/a
20	chr1:92135648-92135698	NHDF-neo	bronchial:	n/a
21	chr1:92135648-92135698	HNPCEpiC	eye:	n/a
22	chr1:92154087-92154137	Jurkat	blood:	n/a
23	chr1:92099528-92099578	HL-60	blood:	n/a
24	chr1:92150549-92150599	Caco-2	colon:	n/a
25	chr1:92179761-92179811	U87	brain:	n/a
26	chr1:92101219-92101269	GM19239	blood:	n/a
27	chr1:92149139-92149189	HAEpiC	amniotic membrane:	n/a
28	chr1:92100107-92100157	Jurkat	blood:	n/a
29	chr1:92135648-92135698	HIPEpiC	eye:	n/a
30	chr1:92100107-92100157	Hepatocyte	liver:	n/a
31	chr1:92101219-92101269	SK-N-MC	brain:	n/a
32	chr1:92171309-92171359	HRE	kidney:	n/a
33	chr1:92203667-92203717	MCF10A-Er-Src	breast:	n/a
34	chr1:92179761-92179811	HAEpiC	amniotic membrane:	n/a
35	chr1:92099528-92099578	NT2-D1	testis:	n/a
36	chr1:92154087-92154137	HPAEpiC	pulmonary alveolar:	n/a
37	chr1:92150549-92150599	GM12891	blood:	n/a
38	chr1:92203667-92203717	PFSK-1	brain:	n/a
39	chr1:92099528-92099578	H1-hESC	embryonic stem cell:	embryo
40	chr1:92179761-92179811	NHBE	bronchial:	n/a
41	chr1:92102055-92102105	BE2_C	brain:	n/a
42	chr1:92203667-92203717	NHDF-neo	bronchial:	n/a
43	chr1:92203667-92203717	SK-N-MC	brain:	n/a
44	chr1:92197531-92197581	HCF	heart:	n/a
45	chr1:92191625-92191675	HCPEpiC	choroid plexus:	n/a
46	chr1:92100082-92100132	RPTEC	kidney:	n/a
47	chr1:92203667-92203717	SK-N-SH	brain:	n/a
48	chr1:92191625-92191675	HUVEC	blood vessel:	n/a
49	chr1:92179761-92179811	AoSMC	blood vessel:	n/a
50	chr1:92100107-92100157	SAEC	small airway:	n/a

(count:105 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr1:92094905..92097332-chr1:92098172..92099750,2	K562	blood:
2	chr1:92169004..92174919-chr1:92176719..92181810,13	K562	blood:
3	chr1:92162441..92164446-chr1:92195933..92198118,2	K562	blood:
4	chr1:92147184..92150173-chr1:92170826..92172983,2	K562	blood:
5	chr1:92169636..92171571-chr1:92175226..92178212,2	K562	blood:
6	chr1:92181357..92183863-chr1:92196120..92197770,2	K562	blood:
7	chr1:92172545..92174973-chr1:92176760..92181587,6	K562	blood:
8	chr1:92140250..92142676-chr1:92166165..92167732,2	K562	blood:
9	chr1:92171820..92173594-chr1:92174594..92176348,2	K562	blood:
10	chr1:92197642..92200532-chr1:92350997..92352784,2	K562	blood:
11	chr1:92118900..92121538-chr1:92139273..92141628,2	MCF-7	breast:
12	chr1:92161234..92163653-chr1:92164578..92167182,3	K562	blood:
13	chr1:92170602..92173339-chr1:92193646..92196655,3	K562	blood:
14	chr1:92160729..92163460-chr1:92181543..92183054,2	K562	blood:
15	chr1:92094905..92097332-chr1:92098172..92099750,2	K562	blood:
16	chr1:92143583..92146461-chr1:92147900..92150725,3	K562	blood:
17	chr1:92186351..92189237-chr1:92195630..92198229,2	K562	blood:
18	chr1:92162419..92166265-chr1:92170255..92173059,5	K562	blood:
19	chr1:92155914..92157539-chr1:92165115..92168054,2	K562	blood:
20	chr1:92155914..92157539-chr1:92165115..92168054,2	K562	blood:
21	chr1:92196960..92199922-chr1:92201744..92205146,4	K562	blood:
22	chr1:92151670..92153207-chr1:92161456..92163644,2	K562	blood:
23	chr1:92194536..92198402-chr1:92243329..92245903,3	K562	blood:
24	chr1:92178299..92180371-chr1:92198181..92200886,2	K562	blood:
25	chr1:92192178..92194320-chr1:92196821..92198679,2	K562	blood:
26	chr1:92171317..92173686-chr1:92182060..92185039,2	K562	blood:
27	chr1:92189258..92193188-chr1:92194522..92196591,3	K562	blood:
28	chr1:92156294..92159210-chr1:92161380..92163036,2	K562	blood:
29	chr1:92197202..92203288-chr1:92206365..92210533,5	K562	blood:
30	chr1:92189655..92191426-chr1:92192587..92194510,2	K562	blood:
31	chr1:92181357..92183863-chr1:92196120..92197770,2	K562	blood:
32	chr1:92119870..92122702-chr1:92124415..92126033,2	MCF-7	breast:
33	chr1:92111029..92113050-chr1:92113299..92116260,2	K562	blood:
34	chr1:92081027..92084138-chr1:92090096..92093775,3	K562	blood:
35	chr1:92186351..92189237-chr1:92195630..92198229,2	K562	blood:
36	chr1:92148164..92151549-chr1:92152320..92156969,4	K562	blood:
37	chr1:92093151..92095190-chr1:92098812..92100312,2	K562	blood:
38	chr1:92151670..92153207-chr1:92161456..92163644,2	K562	blood:
39	chr1:92162419..92166265-chr1:92170255..92173059,5	K562	blood:
40	chr1:92143583..92146461-chr1:92147900..92150725,3	K562	blood:
41	chr1:92166691..92169573-chr1:92171812..92173535,2	K562	blood:
42	chr1:92162419..92165412-chr1:92170320..92173271,4	K562	blood:
43	chr1:92182554..92184890-chr1:92189322..92192184,2	K562	blood:
44	chr1:92180489..92182487-chr1:92191711..92193965,2	K562	blood:
45	chr1:92161234..92163653-chr1:92164578..92167182,3	K562	blood:
46	chr1:92119870..92122702-chr1:92124415..92126033,2	MCF-7	breast:
47	chr1:92177009..92179682-chr1:92195748..92197642,2	K562	blood:
48	chr1:92182554..92184890-chr1:92189322..92192184,2	K562	blood:
49	chr1:92139645..92141947-chr1:92143774..92146003,3	K562	blood:
50	chr1:92197202..92203288-chr1:92206365..92210533,5	K562	blood:

No data

(count:8 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	TGFBR3	hsa-miR-181a-5p	chr1:92147377-92147371
2	TGFBR3	hsa-miR-101-3p	chr1:92146310-92146303
3	TGFBR3	hsa-miR-101-3p	chr1:92146304-92146323
4	TGFBR3	hsa-miR-21-5p	chr1:92148000-92148022
5	TGFBR3	hsa-miR-193b-3p	chr1:92146042-92146036
6	TGFBR3	hsa-miR-21-5p	chr1:92147733-92147755
7	TGFBR3	hsa-miR-101-3p	chr1:92147198-92147219
8	TGFBR3	hsa-miR-193b-3p	chr1:92146036-92146057

Variant related genes	Relation type
TGFBR3	TF binding region
HSP90B3P	TF binding region
TGFBR3	CpG island
HSP90B3P	CpG island
ENSG00000069702	chromatin interactions

Extended variants
information (count: 4693 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:4693 , 50 per page) page: 1 2 3 4 5 6 7 ... 94

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563077072	chr1:92084144-92084145	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs556261136	chr1:92084171-92084172	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs577690691	chr1:92084177-92084178	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs544633453	chr1:92084274-92084275	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs560101988	chr1:92084303-92084304	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs12074345	chr1:92084323-92084324	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs74100990	chr1:92084369-92084370	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs12074375	chr1:92084386-92084387	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs542559443	chr1:92084397-92084398	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs187502533	chr1:92084409-92084410	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs35137032	chr1:92084423-92084424	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs17131508	chr1:92084445-92084446	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs74100991	chr1:92084453-92084454	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs373627357	chr1:92084456-92084457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs562812057	chr1:92084466-92084467	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs533468155	chr1:92084467-92084468	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs551478081	chr1:92084472-92084473	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs566906439	chr1:92084483-92084484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs78539583	chr1:92084484-92084485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs142716700	chr1:92084504-92084505	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs147346562	chr1:92084594-92084595	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs538414053	chr1:92084625-92084626	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs17131509	chr1:92084657-92084658	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs370843122	chr1:92084660-92084661	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs6687718	chr1:92084669-92084670	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs112962603	chr1:92084689-92084690	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs115997052	chr1:92084695-92084696	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs71087964	chr1:92084714-92084715	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs538765190	chr1:92084724-92084725	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs78908510	chr1:92084726-92084727	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs397980795	chr1:92084727-92084728	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs77441270	chr1:92084728-92084729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs570365882	chr1:92084768-92084769	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs148018462	chr1:92084858-92084859	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs375063247	chr1:92084862-92084863	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs141661159	chr1:92084866-92084867	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs111542003	chr1:92084871-92084872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs200488596	chr1:92084887-92084888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs543164312	chr1:92084910-92084911	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs565096105	chr1:92084944-92084945	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs533265674	chr1:92084968-92084969	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs7534256	chr1:92084979-92084980	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs182793694	chr1:92084982-92084983	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs527655799	chr1:92085000-92085001	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs549420682	chr1:92085077-92085078	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs371559511	chr1:92085083-92085084	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs567912549	chr1:92085219-92085220	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs538549073	chr1:92085234-92085235	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs59178722	chr1:92085259-92085260	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs369787749	chr1:92085270-92085271	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	22429812	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17133270	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	16397240	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	22522925	CNVD
Lung adenocarcinoma	21935476	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Prostate cancer	19156837	CNVD
Autism	17483303	CNVD
Malignant melanoma	17260012	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2587 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:92075800-92088200	Weak transcription	Right Atrium	heart
2	chr1:92078000-92088200	Weak transcription	Ovary	ovary
3	chr1:92080000-92085000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr1:92080000-92085000	Weak transcription	NHDF-Ad	bronchial
5	chr1:92080000-92085200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr1:92080000-92087600	Weak transcription	Fetal Heart	heart
7	chr1:92082800-92084200	Enhancers	H1 Cell Line	embryonic stem cell
8	chr1:92082800-92084200	Enhancers	Psoas Muscle	Psoas
9	chr1:92083000-92084600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr1:92083000-92085400	Enhancers	Fetal Muscle Leg	muscle
11	chr1:92083000-92087600	Weak transcription	Skeletal Muscle Male	skeletal muscle
12	chr1:92083400-92088600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr1:92083400-92088600	Weak transcription	Left Ventricle	heart
14	chr1:92083600-92084600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr1:92083600-92084600	Weak transcription	Fetal Muscle Trunk	muscle
16	chr1:92083800-92084200	Enhancers	Fetal Lung	lung
17	chr1:92084000-92084200	Enhancers	Breast Myoepithelial Primary Cells	Breast
18	chr1:92084000-92086800	Weak transcription	Colon Smooth Muscle	Colon
19	chr1:92084000-92087200	Weak transcription	Adipose Nuclei	Adipose
20	chr1:92084000-92087400	Weak transcription	Skeletal Muscle Female	skeletal muscle
21	chr1:92084000-92103200	Weak transcription	HUES64 Cell Line	embryonic stem cell
22	chr1:92084200-92085400	Weak transcription	Fetal Lung	lung
23	chr1:92084200-92086600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
24	chr1:92084600-92085000	Enhancers	Fetal Muscle Trunk	muscle
25	chr1:92084600-92086400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr1:92084600-92086800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr1:92085000-92085400	Enhancers	NHDF-Ad	bronchial
28	chr1:92085000-92085600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr1:92085200-92085800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr1:92085200-92086200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr1:92085400-92085600	Bivalent Enhancer	HSMMtube	muscle
32	chr1:92085400-92085800	Enhancers	Osteobl	bone
33	chr1:92085400-92086000	Enhancers	Muscle Satellite Cultured Cells	--
34	chr1:92085400-92087200	Weak transcription	Fetal Muscle Leg	muscle
35	chr1:92085400-92087400	Weak transcription	NHDF-Ad	bronchial
36	chr1:92085600-92085800	Enhancers	Fetal Lung	lung
37	chr1:92085600-92088000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr1:92086200-92087000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr1:92086400-92087600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr1:92086600-92086800	Enhancers	Brain Inferior Temporal Lobe	brain
41	chr1:92086600-92089200	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr1:92086800-92087600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr1:92086800-92087600	Weak transcription	Brain Inferior Temporal Lobe	brain
44	chr1:92086800-92089000	Enhancers	Colon Smooth Muscle	Colon
45	chr1:92087000-92087200	Enhancers	Psoas Muscle	Psoas
46	chr1:92087000-92089400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr1:92087200-92087400	Enhancers	Fetal Muscle Leg	muscle
48	chr1:92087200-92088600	Enhancers	Adipose Nuclei	Adipose
49	chr1:92087200-92089000	Enhancers	Aorta	Aorta
50	chr1:92087200-92089000	Enhancers	Stomach Smooth Muscle	stomach

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