Variant report

Variant	nsv830332
Chromosome Location	chr5:68238288-68282681
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	BACH1	chr5:68258751-68259013	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCL3	chr5:68260450-68262189	GM12878	blood:	n/a	n/a
3	BCL3	chr5:68260303-68262196	GM12878	blood:	n/a	n/a
4	BRCA1	chr5:68258726-68258984	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr5:68276082-68276203	A549	lung:	n/a	n/a
6	CEBPB	chr5:68239183-68239383	HepG2	liver:	n/a	chr5:68239232-68239243
7	CEBPB	chr5:68264348-68264652	HepG2	liver:	n/a	n/a
8	CHD2	chr5:68258746-68258988	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr5:68258880-68259030	GM12872	blood:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
10	CTCF	chr5:68258820-68258970	HEK293	kidney:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
11	CTCF	chr5:68258797-68259027	GM12878	blood:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
12	CTCF	chr5:68258820-68258970	GM12875	blood:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
13	CTCF	chr5:68258811-68259041	ECC-1	luminal epithelium:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
14	CTCF	chr5:68258836-68258998	GM20000	blood:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
15	CTCF	chr5:68258840-68258990	HBMEC	blood vessel:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
16	CTCF	chr5:68258774-68259047	LNCaP	prostate:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
17	CTCF	chr5:68246480-68246630	HMEC	breast:	n/a	n/a
18	CTCF	chr5:68258860-68259010	WI-38	lung:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
19	CTCF	chr5:68258840-68258990	NHEK	skin:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
20	CTCF	chr5:68258774-68259045	NHEK	skin:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
21	CTCF	chr5:68258820-68258970	HCM	heart:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
22	CTCF	chr5:68258860-68259010	GM12873	blood:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
23	CTCF	chr5:68258840-68258990	AG10803	skin:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
24	CTCF	chr5:68258408-68259294	SK-N-SH	brain:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
25	CTCF	chr5:68258820-68258970	Caco-2	colon:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
26	CTCF	chr5:68258779-68259026	HepG2	liver:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
27	CTCF	chr5:68258800-68258950	MCF-7	breast:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
28	CTCF	chr5:68258820-68258970	HBMEC	blood vessel:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
29	CTCF	chr5:68266822-68266888	MCF-7	breast:	n/a	n/a
30	CTCF	chr5:68258840-68258990	AG09319	gingival:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
31	CTCF	chr5:68258860-68259010	HRE	kidney:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
32	CTCF	chr5:68258727-68259043	H1-hESC	embryonic stem cell:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
33	CTCF	chr5:68258840-68258990	GM12868	blood:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
34	CTCF	chr5:68258790-68259034	GM19240	blood:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
35	CTCF	chr5:68258800-68258950	GM12869	blood:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
36	CTCF	chr5:68258820-68258970	AG09309	skin:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
37	CTCF	chr5:68258800-68258950	NHDF-neo	bronchial:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
38	CTCF	chr5:68281280-68281430	GM12872	blood:	n/a	n/a
39	CTCF	chr5:68258689-68259111	T-47D	breast:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
40	CTCF	chr5:68258820-68258970	GM12865	blood:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
41	CTCF	chr5:68258900-68259050	GM06990	blood:	n/a	n/a
42	CTCF	chr5:68244000-68244150	HCM	heart:	n/a	n/a
43	CTCF	chr5:68266860-68267010	BE2_C	brain:	n/a	n/a
44	CTCF	chr5:68258816-68259020	GM13976	blood:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
45	CTCF	chr5:68258820-68258970	AG04450	lung:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
46	CTCF	chr5:68258860-68259010	GM12868	blood:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
47	CTCF	chr5:68258840-68258990	GM06990	blood:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
48	CTCF	chr5:68258840-68258990	Caco-2	colon:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
49	CTCF	chr5:68258681-68259188	IMR90	lung:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
50	CTCF	chr5:68258813-68259029	H1-hESC	embryonic stem cell:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:68245848-68245898	HRCEpiC	kidney:	n/a
2	chr5:68245848-68245898	AG09319	gingival:	n/a
3	chr5:68245848-68245898	HCT-116	colon:	n/a
4	chr5:68245848-68245898	A549	lung:	n/a
5	chr5:68245848-68245898	ECC-1	luminal epithelium:	n/a
6	chr5:68245848-68245898	PANC-1	pancreas:	n/a
7	chr5:68245848-68245898	HCF	heart:	n/a
8	chr5:68245848-68245898	SK-N-MC	brain:	n/a
9	chr5:68245848-68245898	AG10803	skin:	n/a
10	chr5:68245848-68245898	AG04450	lung:	fetal
11	chr5:68245848-68245898	MCF10A-Er-Src	breast:	n/a
12	chr5:68245848-68245898	Caco-2	colon:	n/a
13	chr5:68245848-68245898	AG09309	skin:	n/a
14	chr5:68245848-68245898	K562	blood:	n/a
15	chr5:68245848-68245898	HMEC	breast:	n/a
16	chr5:68245848-68245898	BE2_C	brain:	n/a
17	chr5:68245848-68245898	HEK293	kidney:	embryo
18	chr5:68245848-68245898	HRPEpiC	eye:	n/a
19	chr5:68245848-68245898	LNCaP	prostate:	n/a
20	chr5:68245848-68245898	ProgFib	skin:	n/a
21	chr5:68245848-68245898	GM19239	blood:	n/a
22	chr5:68245848-68245898	BJ	skin:	n/a
23	chr5:68245848-68245898	NHBE	bronchial:	n/a
24	chr5:68245848-68245898	NH-A	brain:	n/a
25	chr5:68245848-68245898	HL-60	blood:	n/a
26	chr5:68245848-68245898	IMR90	lung:	fetal
27	chr5:68245848-68245898	SAEC	small airway:	n/a
28	chr5:68245848-68245898	NT2-D1	testis:	n/a
29	chr5:68245848-68245898	U87	brain:	n/a
30	chr5:68245848-68245898	T-47D	breast:	n/a
31	chr5:68245848-68245898	HUVEC	blood vessel:	n/a
32	chr5:68245848-68245898	GM12892	blood:	n/a
33	chr5:68245848-68245898	NHDF-neo	bronchial:	n/a
34	chr5:68245848-68245898	PrEC	prostate:	n/a
35	chr5:68245848-68245898	HCM	heart:	n/a
36	chr5:68245848-68245898	HRE	kidney:	n/a
37	chr5:68245848-68245898	RPTEC	kidney:	n/a
38	chr5:68245848-68245898	GM12878	blood:	n/a
39	chr5:68245848-68245898	GM12891	blood:	n/a
40	chr5:68245848-68245898	GM06990	blood:	n/a
41	chr5:68245848-68245898	H1-hESC	embryonic stem cell:	embryo
42	chr5:68245848-68245898	PFSK-1	brain:	n/a
43	chr5:68245848-68245898	AG04449	skin:	fetal
44	chr5:68245848-68245898	AoSMC	blood vessel:	n/a
45	chr5:68245848-68245898	HCPEpiC	choroid plexus:	n/a
46	chr5:68245848-68245898	SK-N-SH	brain:	n/a
47	chr5:68245848-68245898	HIPEpiC	eye:	n/a
48	chr5:68245848-68245898	Jurkat	blood:	n/a
49	chr5:68245848-68245898	HEEpiC	esophagus:	n/a
50	chr5:68245848-68245898	HNPCEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:68251674..68254012-chr5:68255255..68257197,2	K562	blood:
2	chr5:68251674..68254012-chr5:68255255..68257197,2	K562	blood:
3	chr5:68239218..68240904-chr5:68246497..68248439,2	MCF-7	breast:
4	chr5:68234349..68236254-chr5:68237922..68240366,2	K562	blood:
5	chr5:68239218..68240904-chr5:68246497..68248439,2	MCF-7	breast:
6	chr5:68258016..68260416-chr5:68261824..68264961,3	MCF-7	breast:
7	chr5:68248343..68250458-chr5:68251741..68254406,2	K562	blood:
8	chr5:68248343..68250458-chr5:68251741..68254406,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCDC125-5	chr5:68256367-68256453	ENSG00000249335.1
2	lnc-CCDC125-4	chr5:68264370-68264771	XLOC_004860
3	lnc-CCDC125-4	chr5:68265629-68265746	XLOC_004860
4	lnc-CCDC125-4	chr5:68264431-68264771	XLOC_004860
5	lnc-CCDC125-5	chr5:68257696-68257985	ENSG00000249335.1
6	lnc-CCDC125-4	chr5:68264370-68264771	NONHSAT101877
7	lnc-CCDC125-4	chr5:68265940-68266904	XLOC_004860
8	lnc-CCDC125-4	chr5:68265940-68266904	NONHSAT101876
9	lnc-CCDC125-4	chr5:68265629-68265754	XLOC_004860
10	lnc-SLC30A5-1	chr5:68259073-68259310	XLOC_004417
11	lnc-CCDC125-4	chr5:68265629-68265746	NONHSAT101877
12	lnc-CCDC125-4	chr5:68266519-68266904	ENSG00000249352
13	lnc-CCDC125-4	chr5:68264370-68264771	NONHSAT101876
14	lnc-SLC30A5-1	chr5:68263494-68263672	XLOC_004417
15	lnc-CCDC125-4	chr5:68266266-68266579	ENSG00000249352.3
16	lnc-CCDC125-4	chr5:68265629-68265746	XLOC_004860
17	lnc-CCDC125-4	chr5:68263568-68264283	XLOC_004860
18	lnc-CCDC125-4	chr5:68263568-68264283	NONHSAT101876
19	lnc-CCDC125-4	chr5:68264370-68264771	XLOC_004860
20	lnc-CCDC125-4	chr5:68265940-68266904	XLOC_004860
21	lnc-CCDC125-4	chr5:68265629-68265746	NONHSAT101876

Variant related genes	Relation type
ENSG00000250066	TF binding region
ENSG00000249352	TF binding region
ENSG00000249335	TF binding region
ENSG00000250066	CpG island
ENSG00000249352	CpG island
ENSG00000249335	CpG island
ENSG00000250066	chromatin interactions
TNRC6C	miRNA target sites
TOB1	miRNA target sites

Extended variants
information (count: 1392 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:1392 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs62354483	chr5:68238288-68238289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs529199410	chr5:68238317-68238318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs562625056	chr5:68238344-68238345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs542392166	chr5:68238349-68238350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs530063376	chr5:68238391-68238392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs36118348	chr5:68238394-68238395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs371459695	chr5:68238401-68238402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs572620705	chr5:68238409-68238410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs545854779	chr5:68238414-68238415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs564246284	chr5:68238429-68238430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs374486973	chr5:68238452-68238453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs548148724	chr5:68238468-68238469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs566774170	chr5:68238511-68238512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs111552915	chr5:68238522-68238523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs370676911	chr5:68238540-68238541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs533804431	chr5:68238541-68238542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs529973113	chr5:68238553-68238554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs58415037	chr5:68238613-68238614	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs566514626	chr5:68238615-68238616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs527491480	chr5:68238621-68238622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs370136757	chr5:68238635-68238636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs552254721	chr5:68238654-68238655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs6865806	chr5:68238670-68238671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs182792297	chr5:68238671-68238672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs372525831	chr5:68238682-68238683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs537830863	chr5:68238683-68238684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs555918671	chr5:68238717-68238718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs568712218	chr5:68238724-68238725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs141567336	chr5:68238795-68238796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs554460693	chr5:68238796-68238797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs572261538	chr5:68238816-68238817	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs546037025	chr5:68238861-68238862	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs557823076	chr5:68238891-68238892	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs576164220	chr5:68238920-68238921	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs62354484	chr5:68238931-68238932	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs561909156	chr5:68238972-68238973	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs573995178	chr5:68238983-68238984	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs541717617	chr5:68238992-68238993	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs147359393	chr5:68239008-68239009	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs377053991	chr5:68239034-68239035	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs188582325	chr5:68239050-68239051	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs552442409	chr5:68239074-68239075	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs139451816	chr5:68239075-68239076	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs112764096	chr5:68239082-68239083	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs34377543	chr5:68239099-68239100	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs531459829	chr5:68239131-68239132	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs60532552	chr5:68239137-68239138	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs145172929	chr5:68239232-68239233	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs191734647	chr5:68239385-68239386	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs538036068	chr5:68239394-68239395	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17133270	CNVD
Breast cancer	19602461	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	21720365	CNVD
Lung adenocarcinoma	17086460	CNVD
Breast cancer	21045282	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Lung cancer	17086460	CNVD
Prostate cancer	16461572	CNVD
Myelodysplastic syndrome	18663149	CNVD
Spinal muscular atrophy	15981080	CNVD
Spinal muscular atrophy	18839960	CNVD
Spinal muscular atrophy	19716110	CNVD
Sezary syndrome	18413736	CNVD
Ewing''s sarcoma	17952124	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:224 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:68229000-68243200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr5:68238800-68239800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr5:68239800-68242200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr5:68242200-68243400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr5:68242200-68250800	Enhancers	Fetal Lung	lung
6	chr5:68242600-68243000	Enhancers	Adipose Nuclei	Adipose
7	chr5:68243000-68245200	Weak transcription	Adipose Nuclei	Adipose
8	chr5:68243200-68243400	Enhancers	Ovary	ovary
9	chr5:68243400-68245400	Weak transcription	Fetal Heart	heart
10	chr5:68243800-68245000	Weak transcription	Ovary	ovary
11	chr5:68244400-68246400	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr5:68245000-68245200	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr5:68245000-68246200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr5:68245000-68246400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
15	chr5:68245000-68247000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr5:68245000-68247000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
17	chr5:68245000-68247000	Enhancers	Left Ventricle	heart
18	chr5:68245000-68247000	Enhancers	Ovary	ovary
19	chr5:68245000-68247000	Enhancers	Right Atrium	heart
20	chr5:68245200-68246200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr5:68245200-68247200	Enhancers	Adipose Nuclei	Adipose
22	chr5:68245400-68245800	Enhancers	HMEC	breast
23	chr5:68245400-68246200	Enhancers	Placenta	Placenta
24	chr5:68245400-68246400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr5:68245400-68246400	Enhancers	Fetal Muscle Trunk	muscle
26	chr5:68245400-68246800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr5:68245400-68246800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr5:68245400-68246800	Enhancers	Right Ventricle	heart
29	chr5:68245400-68247200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr5:68245400-68247200	Enhancers	Fetal Heart	heart
31	chr5:68245600-68246000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr5:68245600-68246000	Enhancers	Brain Anterior Caudate	brain
33	chr5:68245600-68246000	Enhancers	Brain Cingulate Gyrus	brain
34	chr5:68245600-68246000	Enhancers	Duodenum Smooth Muscle	Duodenum
35	chr5:68245600-68246000	Enhancers	NHEK	skin
36	chr5:68245600-68246200	Enhancers	Brain Inferior Temporal Lobe	brain
37	chr5:68245600-68246200	Enhancers	Esophagus	oesophagus
38	chr5:68245600-68246200	Enhancers	Pancreas	Pancrea
39	chr5:68245600-68246800	Enhancers	Placenta Amnion	Placenta Amnion
40	chr5:68245600-68247000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr5:68245600-68247400	Enhancers	Cortex derived primary cultured neurospheres	brain
42	chr5:68245800-68246000	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr5:68245800-68246000	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
44	chr5:68245800-68246400	Flanking Active TSS	HMEC	breast
45	chr5:68245800-68246600	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr5:68245800-68247000	Enhancers	Brain Hippocampus Middle	brain
47	chr5:68246000-68246400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr5:68246000-68246400	Flanking Active TSS	Brain Anterior Caudate	brain
49	chr5:68246000-68246400	Flanking Active TSS	NHEK	skin
50	chr5:68246000-68246600	Enhancers	iPS-20b Cell Line	embryonic stem cell

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