Variant report

Variant	nsv1019796
Chromosome Location	chr8:10979442-11010826
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	ATF2	chr8:10981506-10982207	GM12878	blood:	n/a	n/a
2	ATF2	chr8:10981488-10982324	GM12878	blood:	n/a	n/a
3	BCLAF1	chr8:10981539-10982080	GM12878	blood:	n/a	n/a
4	BHLHE40	chr8:10981392-10982182	GM12878	blood:	n/a	n/a
5	CEBPB	chr8:11006150-11006516	IMR90	lung:	n/a	chr8:11006326-11006337
6	CEBPB	chr8:11006166-11006493	HepG2	liver:	n/a	chr8:11006326-11006337
7	CEBPB	chr8:10986551-10986831	IMR90	lung:	n/a	n/a
8	CEBPB	chr8:11006185-11006505	K562	blood:	n/a	chr8:11006326-11006337
9	CEBPB	chr8:11006179-11006486	Hela-S3	cervix:	n/a	chr8:11006326-11006337
10	CEBPB	chr8:11006147-11006536	A549	lung:	n/a	chr8:11006326-11006337
11	CEBPB	chr8:11006152-11006488	H1-hESC	embryonic stem cell:	n/a	chr8:11006326-11006337
12	CEBPB	chr8:10984322-10984480	HepG2	liver:	n/a	chr8:10984400-10984411
13	CHD1	chr8:10981485-10982120	GM12878	blood:	n/a	n/a
14	CHD2	chr8:10981673-10981992	GM12878	blood:	n/a	n/a
15	CTCF	chr8:10996820-10996970	WERI-Rb-1	eye:	n/a	chr8:10996901-10996909 chr8:10996892-10996905
16	CTCF	chr8:11001940-11002090	GM12864	blood:	n/a	n/a
17	CTCF	chr8:10996886-10996924	MCF-7	breast:	n/a	chr8:10996901-10996909 chr8:10996892-10996905
18	CTCF	chr8:10996840-10996990	GM12871	blood:	n/a	chr8:10996901-10996909 chr8:10996892-10996905
19	CTCF	chr8:10996820-10996970	SK-N-SH_RA	brain:	n/a	chr8:10996901-10996909 chr8:10996892-10996905
20	CTCF	chr8:10996900-10997050	GM12868	blood:	n/a	chr8:10996901-10996909
21	CTCF	chr8:10996780-10996930	HRE	kidney:	n/a	chr8:10996901-10996909 chr8:10996892-10996905
22	CTCF	chr8:10996860-10997010	SK-N-SH_RA	brain:	n/a	chr8:10996901-10996909 chr8:10996892-10996905
23	CTCF	chr8:11001740-11001890	GM12864	blood:	n/a	n/a
24	CTCF	chr8:10996833-10996970	MCF-7	breast:	n/a	chr8:10996901-10996909 chr8:10996892-10996905
25	CTCF	chr8:10996885-10996936	MCF-7	breast:	n/a	chr8:10996901-10996909 chr8:10996892-10996905
26	CTCF	chr8:10996716-10996997	H1-hESC	embryonic stem cell:	n/a	chr8:10996901-10996909 chr8:10996892-10996905
27	CTCF	chr8:10996820-10996970	HAc	cerebellar:	n/a	chr8:10996901-10996909 chr8:10996892-10996905
28	CTCF	chr8:10996780-10996930	GM12872	blood:	n/a	chr8:10996901-10996909 chr8:10996892-10996905
29	CTCF	chr8:10996828-10996951	MCF-7	breast:	n/a	chr8:10996901-10996909 chr8:10996892-10996905
30	CTCF	chr8:10996820-10996970	HEK293	kidney:	n/a	chr8:10996901-10996909 chr8:10996892-10996905
31	CTCF	chr8:10996800-10996950	GM12871	blood:	n/a	chr8:10996901-10996909 chr8:10996892-10996905
32	CTCF	chr8:10996860-10997010	HEK293	kidney:	n/a	chr8:10996901-10996909 chr8:10996892-10996905
33	CTCF	chr8:10996788-10997008	H1-hESC	embryonic stem cell:	n/a	chr8:10996901-10996909 chr8:10996892-10996905
34	CTCF	chr8:10996820-10996970	HRE	kidney:	n/a	chr8:10996901-10996909 chr8:10996892-10996905
35	CTCF	chr8:10996867-10996944	GM12891	blood:	n/a	chr8:10996901-10996909 chr8:10996892-10996905
36	CTCF	chr8:10996880-10997030	RPTEC	kidney:	n/a	chr8:10996901-10996909 chr8:10996892-10996905
37	CTCF	chr8:10996845-10996957	SK-N-SH_RA	brain:	n/a	chr8:10996901-10996909 chr8:10996892-10996905
38	CTCF	chr8:10996860-10997010	BE2_C	brain:	n/a	chr8:10996901-10996909 chr8:10996892-10996905
39	CTCF	chr8:10996860-10997010	HCPEpiC	choroid plexus:	n/a	chr8:10996901-10996909 chr8:10996892-10996905
40	CTCF	chr8:11001920-11002070	HCPEpiC	choroid plexus:	n/a	n/a
41	CTCF	chr8:10996890-10996925	GM19239	blood:	n/a	chr8:10996901-10996909 chr8:10996892-10996905
42	CTCF	chr8:10996645-10997299	SK-N-SH	brain:	n/a	chr8:10996901-10996909 chr8:10997049-10997057 chr8:10996892-10996905
43	CTCF	chr8:10996860-10997010	GM12869	blood:	n/a	chr8:10996901-10996909 chr8:10996892-10996905
44	CTCF	chr8:11002015-11002027	HUVEC	blood vessel:	n/a	n/a
45	CTCF	chr8:10982701-10982751	GM19239	blood:	n/a	n/a
46	CTCF	chr8:10996860-10997010	GM12872	blood:	n/a	chr8:10996901-10996909 chr8:10996892-10996905
47	CTCF	chr8:10985140-10985290	GM06990	blood:	n/a	n/a
48	CTCF	chr8:10996800-10996950	GM12867	blood:	n/a	chr8:10996901-10996909 chr8:10996892-10996905
49	CTCF	chr8:10996715-10997099	H1-hESC	embryonic stem cell:	n/a	chr8:10996901-10996909 chr8:10997049-10997057 chr8:10996892-10996905
50	CTCF	chr8:10996849-10996946	MCF-7	breast:	n/a	chr8:10996901-10996909 chr8:10996892-10996905

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:10987869-10987919	PFSK-1	brain:	n/a
2	chr8:10996424-10996474	NB4	blood:	n/a
3	chr8:10982668-10982718	ProgFib	skin:	n/a
4	chr8:10982836-10982886	MCF10A-Er-Src	breast:	n/a
5	chr8:10988117-10988167	K562	blood:	n/a
6	chr8:10982836-10982886	NHBE	bronchial:	n/a
7	chr8:10987869-10987919	SAEC	small airway:	n/a
8	chr8:10982332-10982382	SKMC	muscle:	n/a
9	chr8:10982836-10982886	U87	brain:	n/a
10	chr8:10988117-10988167	HRPEpiC	eye:	n/a
11	chr8:10987869-10987919	HEEpiC	esophagus:	n/a
12	chr8:10987869-10987919	HNPCEpiC	eye:	n/a
13	chr8:10982332-10982382	SK-N-SH_RA	brain:	n/a
14	chr8:10987869-10987919	PrEC	prostate:	n/a
15	chr8:10982668-10982718	NT2-D1	testis:	n/a
16	chr8:10982332-10982382	GM06990	blood:	n/a
17	chr8:10996424-10996474	AoSMC	blood vessel:	n/a
18	chr8:10982668-10982718	Hepatocyte	liver:	n/a
19	chr8:10987869-10987919	HRPEpiC	eye:	n/a
20	chr8:10982836-10982886	BJ	skin:	n/a
21	chr8:10982668-10982718	HL-60	blood:	n/a
22	chr8:10982332-10982382	GM12892	blood:	n/a
23	chr8:10982836-10982886	HUVEC	blood vessel:	n/a
24	chr8:10982836-10982886	HCPEpiC	choroid plexus:	n/a
25	chr8:10988117-10988167	AG10803	skin:	n/a
26	chr8:10996424-10996474	GM19239	blood:	n/a
27	chr8:10996424-10996474	SKMC	muscle:	n/a
28	chr8:10987869-10987919	HCT-116	colon:	n/a
29	chr8:10996424-10996474	HMEC	breast:	n/a
30	chr8:10982332-10982382	HRCEpiC	kidney:	n/a
31	chr8:10988117-10988167	HL-60	blood:	n/a
32	chr8:10982332-10982382	T-47D	breast:	n/a
33	chr8:10982668-10982718	GM19239	blood:	n/a
34	chr8:10982836-10982886	SK-N-SH_RA	brain:	n/a
35	chr8:10982836-10982886	HepG2	liver:	n/a
36	chr8:10987869-10987919	HCF	heart:	n/a
37	chr8:10988117-10988167	HAEpiC	amniotic membrane:	n/a
38	chr8:10982836-10982886	GM12891	blood:	n/a
39	chr8:10982668-10982718	HEEpiC	esophagus:	n/a
40	chr8:10982332-10982382	AoSMC	blood vessel:	n/a
41	chr8:10982668-10982718	MCF10A-Er-Src	breast:	n/a
42	chr8:10982332-10982382	HIPEpiC	eye:	n/a
43	chr8:10996424-10996474	MCF10A-Er-Src	breast:	n/a
44	chr8:10987869-10987919	GM12892	blood:	n/a
45	chr8:10982836-10982886	GM12878	blood:	n/a
46	chr8:10982332-10982382	ECC-1	luminal epithelium:	n/a
47	chr8:10988117-10988167	AoSMC	blood vessel:	n/a
48	chr8:10982332-10982382	NT2-D1	testis:	n/a
49	chr8:10982668-10982718	ECC-1	luminal epithelium:	n/a
50	chr8:10982668-10982718	HMEC	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:10987323..10988888-chr8:10996311..10998461,2	MCF-7	breast:
2	chr8:10989309..10991277-chr8:11000364..11001975,2	MCF-7	breast:
3	chr8:10989309..10991277-chr8:11000364..11001975,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AF131215.3.1-1	chr8:10980891-10982327	ENSG00000254936.3
2	lnc-AF131215.3.1-1	chr8:10983271-10983574	ENSG00000254936.3
3	lnc-AF131215.3.1-1	chr8:10980891-10982327	NONHSAT125036
4	lnc-AF131215.3.1-2	chr8:10986134-10987275	NONHSAT125039
5	lnc-MTMR9-1	chr8:10983268-10983574	ENSG00000247665
6	lnc-MTMR9-1	chr8:10980891-10982326	ENSG00000247665
7	lnc-AF131215.3.1-2	chr8:10984315-10984600	NONHSAT125039
8	lnc-AF131215.4.1-1	chr8:10994408-10996117	ENSG00000254556.1
9	lnc-AF131215.3.1-1	chr8:10983268-10983574	ENSG00000254936.3
10	lnc-AF131215.3.1-1	chr8:10980891-10982327	ENSG00000254936.3

Variant related genes	Relation type
ENSG00000254936	TF binding region
ENSG00000215346	TF binding region
ENSG00000254556	TF binding region
ENSG00000254936	CpG island
ENSG00000215346	CpG island
ENSG00000254556	CpG island
ENSG00000215346	chromatin interactions
ZFYVE20	miRNA target sites
KIF5C	miRNA target sites

Extended variants
information (count: 1794 )
Associated
traits (count: 138 )

Variant overlapped rSNPs/rCNVs (count:1794 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs151004334	chr8:10979458-10979459	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs372756673	chr8:10979477-10979478	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs575613268	chr8:10979480-10979481	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs140905207	chr8:10979500-10979501	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs536887365	chr8:10979503-10979504	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs552443825	chr8:10979513-10979514	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs150169594	chr8:10979515-10979516	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs73547404	chr8:10979524-10979525	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs116454649	chr8:10979542-10979543	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs2409709	chr8:10979553-10979554	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs4333549	chr8:10979561-10979562	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs79983241	chr8:10979575-10979576	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs575895109	chr8:10979583-10979584	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs546125856	chr8:10979622-10979623	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs564777437	chr8:10979645-10979646	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs138676394	chr8:10979656-10979657	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs74673974	chr8:10979669-10979670	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs2898263	chr8:10979672-10979673	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs529642915	chr8:10979680-10979681	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs574808262	chr8:10979684-10979685	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs541956786	chr8:10979685-10979686	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs536476604	chr8:10979699-10979700	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs186983874	chr8:10979700-10979701	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs563091327	chr8:10979736-10979737	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs529629445	chr8:10979794-10979795	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs2409710	chr8:10979821-10979822	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs552122215	chr8:10979849-10979850	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs570642627	chr8:10979852-10979853	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs528350348	chr8:10979862-10979863	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs114494497	chr8:10979888-10979889	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs57308044	chr8:10979955-10979956	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs535894631	chr8:10979957-10979958	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs557485757	chr8:10979985-10979986	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs569400618	chr8:10979990-10979991	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs540005229	chr8:10980013-10980014	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs115818059	chr8:10980038-10980039	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs573406046	chr8:10980042-10980043	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs141566016	chr8:10980044-10980045	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs551943794	chr8:10980063-10980064	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs544252581	chr8:10980073-10980074	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs555649526	chr8:10980113-10980114	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs369875573	chr8:10980118-10980119	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs574092296	chr8:10980121-10980122	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs183658145	chr8:10980124-10980125	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs188855900	chr8:10980174-10980175	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs530488692	chr8:10980179-10980180	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs74711708	chr8:10980215-10980216	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs564082971	chr8:10980221-10980222	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs540515944	chr8:10980229-10980230	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs71518510	chr8:10980269-10980270	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:138)

Disease	PMID	Source
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
Prostate cancer	16573809	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Developmental disorder	20461109	CNVD
abnormal development	18461090	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Gastric cancer	21811585	CNVD
Colorectal cancer	16774939	CNVD
Breast cancer	22522925	CNVD
Acute lymphoblastic leukemia	21390130	CNVD

Chromatin state (count:324 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:10963000-10981200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
2	chr8:10965800-10981600	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr8:10966200-10981400	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr8:10966200-10999000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr8:10966400-11026200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr8:10975000-10981000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr8:10975000-10981200	Weak transcription	Primary T helper cells PMA-I stimulated	--
8	chr8:10975600-10981000	Weak transcription	Primary T helper cells fromperipheralblood	blood
9	chr8:10975600-10981400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
10	chr8:10975800-10980400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
11	chr8:10975800-10981200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
12	chr8:10978000-10981200	Weak transcription	Primary B cells from peripheral blood	blood
13	chr8:10979400-10979600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
14	chr8:10979400-10979600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
15	chr8:10979400-10980400	ZNF genes & repeats	GM12878-XiMat	blood
16	chr8:10980000-10981400	Weak transcription	HUES6 Cell Line	embryonic stem cell
17	chr8:10980200-10981200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
18	chr8:10980400-10980800	Enhancers	GM12878-XiMat	blood
19	chr8:10980400-10981400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
20	chr8:10980600-10982000	Enhancers	Primary hematopoietic stem cells	blood
21	chr8:10980800-10981400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr8:10980800-10981600	Flanking Active TSS	GM12878-XiMat	blood
23	chr8:10981000-10981200	Enhancers	Primary hematopoietic stem cells short term culture	blood
24	chr8:10981000-10981200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr8:10981000-10981400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
26	chr8:10981000-10981400	Enhancers	Primary T helper cells fromperipheralblood	blood
27	chr8:10981000-10981400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
28	chr8:10981000-10981600	Enhancers	Primary T killer memory cells from peripheral blood	blood
29	chr8:10981200-10981400	Enhancers	Primary T cells fromperipheralblood	blood
30	chr8:10981200-10981400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
31	chr8:10981200-10981400	Enhancers	Primary T helper naive cells from peripheral blood	blood
32	chr8:10981200-10981400	Enhancers	Primary T helper cells PMA-I stimulated	--
33	chr8:10981200-10981400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
34	chr8:10981200-10981400	Enhancers	Duodenum Mucosa	Duodenum
35	chr8:10981200-10981600	Enhancers	Primary B cells from cord blood	blood
36	chr8:10981200-10981600	Enhancers	Primary B cells from peripheral blood	blood
37	chr8:10981200-10981600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
38	chr8:10981200-10981600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
39	chr8:10981200-10981600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
40	chr8:10981200-10981600	Enhancers	Spleen	Spleen
41	chr8:10981200-10982200	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr8:10981200-10982400	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
43	chr8:10981200-10982800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr8:10981400-10981600	Flanking Active TSS	Primary T cells fromperipheralblood	blood
45	chr8:10981400-10981600	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
46	chr8:10981400-10981600	Flanking Active TSS	Duodenum Mucosa	Duodenum
47	chr8:10981400-10982000	Enhancers	HUES6 Cell Line	embryonic stem cell
48	chr8:10981400-10982200	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
49	chr8:10981400-10982200	Active TSS	Rectal Mucosa Donor 29	rectum
50	chr8:10981400-10982400	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood

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