Variant report

Variant	nsv529002
Chromosome Location	chr1:95781217-95805002
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr1:95786650-95786850	HepG2	liver:	n/a	chr1:95786681-95786692
2	CEBPB	chr1:95788853-95788988	HepG2	liver:	n/a	n/a
3	CEBPB	chr1:95793144-95793154	HepG2	liver:	n/a	n/a
4	CTCF	chr1:95801147-95801220	ProgFib	skin:	n/a	n/a
5	CTCF	chr1:95793620-95793658	K562	blood:	n/a	n/a
6	CTCF	chr1:95793600-95793750	HEEpiC	esophagus:	n/a	n/a
7	CTCF	chr1:95793560-95793710	HPF	lung:	n/a	n/a
8	CTCF	chr1:95793540-95793690	HMEC	breast:	n/a	n/a
9	CTCF	chr1:95793560-95793710	HMEC	breast:	n/a	n/a
10	CTCF	chr1:95798214-95798310	GM20000	blood:	n/a	n/a
11	CTCF	chr1:95793600-95793750	HRPEpiC	eye:	n/a	n/a
12	CTCF	chr1:95793655-95793721	K562	blood:	n/a	n/a
13	EP300	chr1:95788466-95792016	SK-N-SH	brain:	n/a	chr1:95788868-95788877 chr1:95790953-95790963 chr1:95791561-95791575 chr1:95788869-95788878
14	EP300	chr1:95796279-95796292	HepG2	liver:	n/a	n/a
15	FAM48A	chr1:95793471-95793500	GM12878	blood:	n/a	n/a
16	FOS	chr1:95788703-95789042	HUVEC	blood vessel:	n/a	chr1:95788868-95788878 chr1:95788870-95788877 chr1:95788868-95788877 chr1:95788867-95788878 chr1:95788869-95788878 chr1:95788869-95788877 chr1:95788867-95788879
17	FOS	chr1:95788705-95789051	MCF10A-Er-Src	breast:	n/a	chr1:95788868-95788878 chr1:95788870-95788877 chr1:95788868-95788877 chr1:95788867-95788878 chr1:95788869-95788878 chr1:95788869-95788877 chr1:95788867-95788879
18	FOS	chr1:95788706-95789053	MCF10A-Er-Src	breast:	n/a	chr1:95788868-95788878 chr1:95788870-95788877 chr1:95788868-95788877 chr1:95788867-95788878 chr1:95788869-95788878 chr1:95788869-95788877 chr1:95788867-95788879
19	FOS	chr1:95788707-95789039	MCF10A-Er-Src	breast:	n/a	chr1:95788868-95788878 chr1:95788870-95788877 chr1:95788868-95788877 chr1:95788867-95788878 chr1:95788869-95788878 chr1:95788869-95788877 chr1:95788867-95788879
20	FOS	chr1:95788709-95789050	MCF10A-Er-Src	breast:	n/a	chr1:95788868-95788878 chr1:95788870-95788877 chr1:95788868-95788877 chr1:95788867-95788878 chr1:95788869-95788878 chr1:95788869-95788877 chr1:95788867-95788879
21	FOSL1	chr1:95788669-95789093	HCT-116	colon:	n/a	chr1:95788868-95788878 chr1:95788870-95788877 chr1:95788868-95788877 chr1:95788869-95788878 chr1:95788869-95788877 chr1:95788867-95788879
22	FOSL2	chr1:95788703-95789009	HepG2	liver:	n/a	chr1:95788868-95788878 chr1:95788868-95788879 chr1:95788870-95788877 chr1:95788868-95788877 chr1:95788869-95788878 chr1:95788869-95788877 chr1:95788867-95788879
23	FOSL2	chr1:95788730-95789078	HepG2	liver:	n/a	chr1:95788868-95788878 chr1:95788868-95788879 chr1:95788870-95788877 chr1:95788868-95788877 chr1:95788869-95788878 chr1:95788869-95788877 chr1:95788867-95788879
24	GATA2	chr1:95790760-95791300	SH-SY5Y	brain:	n/a	n/a
25	GATA2	chr1:95789286-95789559	SH-SY5Y	brain:	n/a	chr1:95789463-95789472
26	GATA2	chr1:95789839-95790352	SH-SY5Y	brain:	n/a	n/a
27	GATA3	chr1:95790929-95791218	SH-SY5Y	brain:	n/a	n/a
28	GATA3	chr1:95790117-95790436	SH-SY5Y	brain:	n/a	n/a
29	JUN	chr1:95785989-95786099	K562	blood:	n/a	n/a
30	JUN	chr1:95788757-95789033	HepG2	liver:	n/a	chr1:95788868-95788878 chr1:95788870-95788877 chr1:95788868-95788877 chr1:95788869-95788878 chr1:95788869-95788877 chr1:95788867-95788879
31	JUND	chr1:95788742-95788938	HepG2	liver:	n/a	chr1:95788868-95788878 chr1:95788870-95788877 chr1:95788868-95788877 chr1:95788867-95788878 chr1:95788869-95788878 chr1:95788869-95788877 chr1:95788867-95788879
32	JUND	chr1:95788694-95789059	HepG2	liver:	n/a	chr1:95788868-95788878 chr1:95788870-95788877 chr1:95788868-95788877 chr1:95788867-95788878 chr1:95788869-95788878 chr1:95788869-95788877 chr1:95788867-95788879
33	JUND	chr1:95788555-95789194	SK-N-SH	brain:	n/a	chr1:95788868-95788878 chr1:95788870-95788877 chr1:95788868-95788877 chr1:95788867-95788878 chr1:95788869-95788878 chr1:95788869-95788877 chr1:95788867-95788879
34	JUND	chr1:95788729-95789037	Hela-S3	cervix:	n/a	chr1:95788868-95788878 chr1:95788870-95788877 chr1:95788868-95788877 chr1:95788867-95788878 chr1:95788869-95788878 chr1:95788869-95788877 chr1:95788867-95788879
35	JUND	chr1:95788796-95788918	HepG2	liver:	n/a	chr1:95788868-95788878 chr1:95788870-95788877 chr1:95788868-95788877 chr1:95788867-95788878 chr1:95788869-95788878 chr1:95788869-95788877 chr1:95788867-95788879
36	JUND	chr1:95788680-95789067	H1-hESC	embryonic stem cell:	n/a	chr1:95788868-95788878 chr1:95788870-95788877 chr1:95788868-95788877 chr1:95788867-95788878 chr1:95788869-95788878 chr1:95788869-95788877 chr1:95788867-95788879
37	JUND	chr1:95788748-95789013	K562	blood:	n/a	chr1:95788868-95788878 chr1:95788870-95788877 chr1:95788868-95788877 chr1:95788867-95788878 chr1:95788869-95788878 chr1:95788869-95788877 chr1:95788867-95788879
38	MYC	chr1:95802809-95802975	MCF10A-Er-Src	breast:	n/a	n/a
39	NR3C1	chr1:95798387-95798654	A549	lung:	n/a	chr1:95798437-95798463 chr1:95798440-95798461 chr1:95798454-95798475 chr1:95798456-95798472 chr1:95798437-95798463 chr1:95798451-95798477 chr1:95798442-95798458 chr1:95798443-95798457 chr1:95798437-95798463 chr1:95798456-95798472 chr1:95798451-95798477 chr1:95798442-95798458 chr1:95798451-95798477 chr1:95798508-95798526 chr1:95798437-95798463 chr1:95798457-95798471 chr1:95798441-95798459 chr1:95798443-95798457 chr1:95798456-95798471 chr1:95798443-95798457 chr1:95798442-95798457
40	NRF1	chr1:95786454-95786469	H1-hESC	embryonic stem cell:	n/a	n/a
41	POLR2A	chr1:95797218-95797286	MCF-7	breast:	n/a	n/a
42	POLR2A	chr1:95796934-95797175	GM12878	blood:	n/a	n/a
43	POLR2A	chr1:95789275-95789333	H1-hESC	embryonic stem cell:	n/a	n/a
44	POLR2A	chr1:95785245-95785279	A549	lung:	n/a	n/a
45	RAD21	chr1:95793590-95793703	Hela-S3	cervix:	n/a	n/a
46	RFX5	chr1:95796175-95796179	K562	blood:	n/a	n/a
47	TBP	chr1:95799199-95799203	K562	blood:	n/a	n/a
48	USF2	chr1:95790902-95790937	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:95783866-95783916	HCF	heart:	n/a
2	chr1:95784493-95784543	AG10803	skin:	n/a
3	chr1:95783866-95783916	NB4	blood:	n/a
4	chr1:95784493-95784543	HCF	heart:	n/a
5	chr1:95784493-95784543	PANC-1	pancreas:	n/a
6	chr1:95784493-95784543	HCPEpiC	choroid plexus:	n/a
7	chr1:95783866-95783916	HCPEpiC	choroid plexus:	n/a
8	chr1:95783866-95783916	HUVEC	blood vessel:	n/a
9	chr1:95783866-95783916	ovcar-3	ovarian:	n/a
10	chr1:95783866-95783916	Caco-2	colon:	n/a
11	chr1:95783866-95783916	Hepatocyte	liver:	n/a
12	chr1:95783866-95783916	NHBE	bronchial:	n/a
13	chr1:95784493-95784543	HL-60	blood:	n/a
14	chr1:95784493-95784543	HAEpiC	amniotic membrane:	n/a
15	chr1:95783866-95783916	AG09309	skin:	n/a
16	chr1:95783866-95783916	HRE	kidney:	n/a
17	chr1:95783866-95783916	T-47D	breast:	n/a
18	chr1:95784493-95784543	SK-N-MC	brain:	n/a
19	chr1:95783866-95783916	ProgFib	skin:	n/a
20	chr1:95784493-95784543	HUVEC	blood vessel:	n/a
21	chr1:95784493-95784543	RPTEC	kidney:	n/a
22	chr1:95784493-95784543	Hela-S3	cervix:	n/a
23	chr1:95783866-95783916	HRCEpiC	kidney:	n/a
24	chr1:95784493-95784543	PFSK-1	brain:	n/a
25	chr1:95784493-95784543	GM12891	blood:	n/a
26	chr1:95783866-95783916	U87	brain:	n/a
27	chr1:95783866-95783916	SK-N-MC	brain:	n/a
28	chr1:95783866-95783916	PFSK-1	brain:	n/a
29	chr1:95784493-95784543	NHBE	bronchial:	n/a
30	chr1:95783866-95783916	ECC-1	luminal epithelium:	n/a
31	chr1:95783866-95783916	GM06990	blood:	n/a
32	chr1:95784493-95784543	PrEC	prostate:	n/a
33	chr1:95784493-95784543	HEK293	kidney:	embryo
34	chr1:95784493-95784543	ovcar-3	ovarian:	n/a
35	chr1:95783866-95783916	Hela-S3	cervix:	n/a
36	chr1:95784493-95784543	LNCaP	prostate:	n/a
37	chr1:95784493-95784543	NB4	blood:	n/a
38	chr1:95783866-95783916	HMEC	breast:	n/a
39	chr1:95783866-95783916	A549	lung:	n/a
40	chr1:95784493-95784543	AG04450	lung:	fetal
41	chr1:95784493-95784543	H1-hESC	embryonic stem cell:	embryo
42	chr1:95784493-95784543	GM19239	blood:	n/a
43	chr1:95784493-95784543	GM12878	blood:	n/a
44	chr1:95784493-95784543	HMEC	breast:	n/a
45	chr1:95783866-95783916	HepG2	liver:	n/a
46	chr1:95783866-95783916	NT2-D1	testis:	n/a
47	chr1:95784493-95784543	ProgFib	skin:	n/a
48	chr1:95784493-95784543	BE2_C	brain:	n/a
49	chr1:95783866-95783916	AoSMC	blood vessel:	n/a
50	chr1:95783866-95783916	PrEC	prostate:	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ALG14-3	chr1:95783467-95783539	XLOC_000927
2	lnc-ALG14-3	chr1:95781384-95781530	XLOC_000927
3	lnc-ALG14-3	chr1:95782438-95782493	XLOC_000927
4	lnc-ALG14-3	chr1:95783704-95783970	XLOC_000927
5	lnc-RWDD3-1	chr1:95783150-95783970	NONHSAT004662
6	lnc-ALG14-3	chr1:95781345-95781530	XLOC_000927
7	lnc-RWDD3-1	chr1:95782437-95782493	NONHSAT004662
8	lnc-ALG14-3	chr1:95782438-95782493	XLOC_000927
9	lnc-ALG14-3	chr1:95783704-95783849	NONHSAT004663
10	lnc-RWDD3-1	chr1:95786849-95787167	NONHSAT004662
11	lnc-RWDD3-1	chr1:95781344-95781530	NONHSAT004662
12	lnc-ALG14-3	chr1:95781388-95781530	NONHSAT004666
13	lnc-RWDD3-2	chr1:95783151-95783713	XLOC_000308
14	lnc-ALG14-3	chr1:95783704-95783849	NONHSAT004666
15	lnc-RWDD3-2	chr1:95786850-95787167	XLOC_000308
16	lnc-ALG14-3	chr1:95783704-95783819	XLOC_000927

Variant related genes	Relation type
ENSG00000228504	TF binding region
ENSG00000228504	CpG island
SLC44A2	miRNA target sites
LPGAT1	miRNA target sites
PRKAA1	miRNA target sites
ZCCHC24	miRNA target sites
FAM122A	miRNA target sites
FAM129A	miRNA target sites

Extended variants
information (count: 637 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:637 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs202221620	chr1:95781217-95781218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs553994343	chr1:95781331-95781332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs376366963	chr1:95781338-95781339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs116623094	chr1:95781344-95781345	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
5	rs187856016	chr1:95781360-95781361	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
6	rs548756043	chr1:95781379-95781380	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
7	rs373269864	chr1:95781399-95781400	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
8	rs562093715	chr1:95781401-95781402	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
9	rs17113357	chr1:95781422-95781423	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs369551844	chr1:95781423-95781424	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
11	rs549430383	chr1:95781455-95781456	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
12	rs527493074	chr1:95781486-95781487	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
13	rs192986523	chr1:95781507-95781508	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
14	rs538222542	chr1:95781550-95781551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs544829174	chr1:95781572-95781573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs183760808	chr1:95781583-95781584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs77206450	chr1:95781598-95781599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs188433339	chr1:95781629-95781630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs11165373	chr1:95781632-95781633	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs56020320	chr1:95781674-95781675	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs537260997	chr1:95781711-95781712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs12135810	chr1:95781729-95781730	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs577442299	chr1:95781753-95781754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs12125618	chr1:95781754-95781755	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs559529669	chr1:95781765-95781766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs147835401	chr1:95781788-95781789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs191457518	chr1:95781809-95781810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs562419906	chr1:95781811-95781812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs11804410	chr1:95781873-95781874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs530992463	chr1:95781885-95781886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs184727526	chr1:95781896-95781897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs76975943	chr1:95781929-95781930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs74104812	chr1:95781936-95781937	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs376858848	chr1:95781946-95781947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs569755073	chr1:95781950-95781951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs190718081	chr1:95781958-95781959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs370275325	chr1:95781986-95781987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs11165374	chr1:95782002-95782003	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs552039683	chr1:95782020-95782021	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs571961480	chr1:95782021-95782022	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs568380327	chr1:95782035-95782036	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs142418607	chr1:95782040-95782041	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs11165375	chr1:95782072-95782073	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs577407685	chr1:95782115-95782116	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs539901843	chr1:95782120-95782121	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs553452042	chr1:95782167-95782168	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs568619379	chr1:95782205-95782206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs554514060	chr1:95782218-95782219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs151277983	chr1:95782219-95782220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs555759958	chr1:95782222-95782223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
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
Medulloblastoma	21979893	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
Multiple myeloma	17550852	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Autism	17483303	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Intestinal disease	21956041	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Gastric cancer	16891809	CNVD
Schizophrenia	17879154	CNVD
Mental retardation	17124404	CNVD
Intestinal disease	17828263	CNVD
Malignant melanoma	17260012	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:104 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:95769200-95782000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr1:95774400-95786800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr1:95777000-95786800	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr1:95782000-95782200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr1:95782200-95785600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr1:95783800-95784200	Enhancers	Cortex derived primary cultured neurospheres	brain
7	chr1:95784200-95786600	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr1:95785200-95785400	Flanking Bivalent TSS/Enh	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr1:95785200-95785400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr1:95785400-95787000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr1:95786600-95786800	Enhancers	Cortex derived primary cultured neurospheres	brain
12	chr1:95786600-95786800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr1:95786600-95786800	Enhancers	Brain Cingulate Gyrus	brain
14	chr1:95786600-95786800	Enhancers	Brain Germinal Matrix	brain
15	chr1:95786600-95786800	Enhancers	Fetal Lung	lung
16	chr1:95786600-95787000	Active TSS	Brain Substantia Nigra	brain
17	chr1:95786600-95787400	Active TSS	Brain Anterior Caudate	brain
18	chr1:95786600-95787400	Active TSS	Brain Hippocampus Middle	brain
19	chr1:95786800-95787000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr1:95786800-95787200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr1:95786800-95787200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr1:95786800-95787200	Flanking Active TSS	Brain Germinal Matrix	brain
23	chr1:95786800-95787200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
24	chr1:95786800-95787200	Active TSS	Fetal Brain Female	brain
25	chr1:95786800-95787200	Flanking Active TSS	Fetal Lung	lung
26	chr1:95786800-95787200	Active TSS	NHDF-Ad	bronchial
27	chr1:95786800-95787400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
28	chr1:95786800-95787400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr1:95786800-95787400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr1:95786800-95787400	Active TSS	Brain Angular Gyrus	brain
31	chr1:95786800-95787400	Active TSS	Brain Inferior Temporal Lobe	brain
32	chr1:95786800-95787800	Flanking Active TSS	Brain Cingulate Gyrus	brain
33	chr1:95786800-95789200	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr1:95786800-95789600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr1:95787000-95787200	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr1:95787000-95787200	Flanking Active TSS	Brain Substantia Nigra	brain
37	chr1:95787000-95787800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr1:95787000-95787800	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr1:95787000-95788200	Enhancers	Fetal Brain Male	brain
40	chr1:95787000-95789400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr1:95787200-95787400	Active TSS	Brain Substantia Nigra	brain
42	chr1:95787200-95787400	Flanking Active TSS	Fetal Brain Female	brain
43	chr1:95787200-95787400	Active TSS	Fetal Lung	lung
44	chr1:95787200-95787600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr1:95787200-95787600	Weak transcription	NHDF-Ad	bronchial
46	chr1:95787200-95787800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr1:95787200-95788000	Enhancers	Brain Germinal Matrix	brain
48	chr1:95787200-95788200	Weak transcription	HUES6 Cell Line	embryonic stem cell
49	chr1:95787400-95787600	Enhancers	Brain Angular Gyrus	brain
50	chr1:95787400-95787800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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