Variant report

Variant	nsv465435
Chromosome Location	chr8:6118630-6253232
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	ARID3A	chr8:6201384-6201656	HepG2	liver:	n/a	n/a
2	BATF	chr8:6125905-6126127	GM12878	blood:	n/a	n/a
3	BHLHE40	chr8:6188926-6189013	K562	blood:	n/a	n/a
4	BHLHE40	chr8:6149426-6149734	GM12878	blood:	n/a	n/a
5	CEBPB	chr8:6128437-6128476	K562	blood:	n/a	n/a
6	CEBPB	chr8:6148528-6148743	HepG2	liver:	n/a	chr8:6148625-6148638 chr8:6148625-6148638 chr8:6148626-6148637 chr8:6148625-6148636
7	CEBPB	chr8:6200012-6200084	A549	lung:	n/a	n/a
8	CEBPB	chr8:6231017-6231102	HepG2	liver:	n/a	n/a
9	CEBPB	chr8:6128430-6128600	HepG2	liver:	n/a	n/a
10	CEBPB	chr8:6132470-6132485	HepG2	liver:	n/a	n/a
11	CEBPB	chr8:6165763-6166327	K562	blood:	n/a	chr8:6165822-6165835 chr8:6165824-6165833 chr8:6165822-6165833
12	CEBPB	chr8:6165771-6165947	A549	lung:	n/a	chr8:6165822-6165835 chr8:6165824-6165833 chr8:6165822-6165833
13	CEBPB	chr8:6229207-6229307	HepG2	liver:	n/a	chr8:6229236-6229247
14	CEBPB	chr8:6229956-6230363	HepG2	liver:	n/a	n/a
15	CEBPB	chr8:6230120-6230328	IMR90	lung:	n/a	n/a
16	CEBPB	chr8:6165750-6165958	HepG2	liver:	n/a	chr8:6165822-6165835 chr8:6165824-6165833 chr8:6165822-6165833
17	CEBPB	chr8:6165750-6165950	IMR90	lung:	n/a	chr8:6165822-6165835 chr8:6165824-6165833 chr8:6165822-6165833
18	CEBPB	chr8:6128333-6128520	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr8:6229961-6230353	A549	lung:	n/a	n/a
20	CHD1	chr8:6188534-6188648	H1-hESC	embryonic stem cell:	n/a	n/a
21	CREB1	chr8:6193500-6193847	GM12878	blood:	n/a	n/a
22	CREB1	chr8:6193467-6193873	GM12878	blood:	n/a	n/a
23	CTCF	chr8:6232200-6232350	GM12867	blood:	n/a	chr8:6232214-6232235 chr8:6232220-6232236 chr8:6232224-6232232 chr8:6232221-6232234
24	CTCF	chr8:6188860-6189010	GM12866	blood:	n/a	chr8:6188961-6188982 chr8:6188968-6188981 chr8:6188968-6188981 chr8:6188966-6188984
25	CTCF	chr8:6140640-6140790	GM12866	blood:	n/a	chr8:6140735-6140753 chr8:6140730-6140751
26	CTCF	chr8:6188880-6189030	HBMEC	blood vessel:	n/a	chr8:6188961-6188982 chr8:6188968-6188981 chr8:6188968-6188981 chr8:6188966-6188984
27	CTCF	chr8:6140686-6140835	GM12892	blood:	n/a	chr8:6140735-6140753 chr8:6140730-6140751
28	CTCF	chr8:6232140-6232290	GM12871	blood:	n/a	chr8:6232214-6232235 chr8:6232220-6232236 chr8:6232224-6232232 chr8:6232221-6232234
29	CTCF	chr8:6229780-6229930	A549	lung:	n/a	n/a
30	CTCF	chr8:6232140-6232290	HPF	lung:	n/a	chr8:6232214-6232235 chr8:6232220-6232236 chr8:6232224-6232232 chr8:6232221-6232234
31	CTCF	chr8:6147164-6147366	H1-hESC	embryonic stem cell:	n/a	chr8:6147257-6147270
32	CTCF	chr8:6188820-6188970	NHDF-neo	bronchial:	n/a	n/a
33	CTCF	chr8:6229800-6229950	SAEC	small airway:	n/a	n/a
34	CTCF	chr8:6126841-6126881	GM13976	blood:	n/a	n/a
35	CTCF	chr8:6147121-6147372	K562	blood:	n/a	chr8:6147257-6147270
36	CTCF	chr8:6140640-6140790	GM06990	blood:	n/a	chr8:6140735-6140753 chr8:6140730-6140751
37	CTCF	chr8:6188740-6188890	WI-38	lung:	n/a	n/a
38	CTCF	chr8:6140651-6140824	MCF-7	breast:	n/a	chr8:6140735-6140753 chr8:6140730-6140751
39	CTCF	chr8:6140600-6140750	SAEC	small airway:	n/a	n/a
40	CTCF	chr8:6229831-6229848	GM10266	blood:	n/a	n/a
41	CTCF	chr8:6188880-6189030	AG09319	gingival:	n/a	chr8:6188961-6188982 chr8:6188968-6188981 chr8:6188968-6188981 chr8:6188966-6188984
42	CTCF	chr8:6140680-6140830	GM12864	blood:	n/a	chr8:6140735-6140753 chr8:6140730-6140751
43	CTCF	chr8:6185460-6185610	A549	lung:	n/a	chr8:6185537-6185550 chr8:6185536-6185552
44	CTCF	chr8:6232160-6232310	GM12866	blood:	n/a	chr8:6232214-6232235 chr8:6232220-6232236 chr8:6232224-6232232 chr8:6232221-6232234
45	CTCF	chr8:6188880-6189030	GM12875	blood:	n/a	chr8:6188961-6188982 chr8:6188968-6188981 chr8:6188968-6188981 chr8:6188966-6188984
46	CTCF	chr8:6232180-6232330	GM12872	blood:	n/a	chr8:6232214-6232235 chr8:6232220-6232236 chr8:6232224-6232232 chr8:6232221-6232234
47	CTCF	chr8:6185500-6185650	Hela-S3	cervix:	n/a	chr8:6185537-6185550 chr8:6185536-6185552
48	CTCF	chr8:6188880-6189030	HPAF	blood vessel:	n/a	chr8:6188961-6188982 chr8:6188968-6188981 chr8:6188968-6188981 chr8:6188966-6188984
49	CTCF	chr8:6232116-6232350	Hela-S3	cervix:	n/a	chr8:6232214-6232235 chr8:6232220-6232236 chr8:6232224-6232232 chr8:6232221-6232234
50	CTCF	chr8:6236785-6236851	Lung_OC	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:6189008-6189058	NH-A	brain:	n/a
2	chr8:6189008-6189058	PFSK-1	brain:	n/a
3	chr8:6189008-6189058	H1-hESC	embryonic stem cell:	embryo
4	chr8:6189008-6189058	K562	blood:	n/a
5	chr8:6189008-6189058	GM19239	blood:	n/a
6	chr8:6189008-6189058	SAEC	small airway:	n/a
7	chr8:6189008-6189058	HEK293	kidney:	embryo
8	chr8:6189008-6189058	HRPEpiC	eye:	n/a
9	chr8:6189008-6189058	HCT-116	colon:	n/a
10	chr8:6189008-6189058	HepG2	liver:	n/a
11	chr8:6189008-6189058	SK-N-MC	brain:	n/a
12	chr8:6189008-6189058	HCPEpiC	choroid plexus:	n/a
13	chr8:6189008-6189058	MCF-7	breast:	n/a
14	chr8:6189008-6189058	Hela-S3	cervix:	n/a
15	chr8:6189008-6189058	HEEpiC	esophagus:	n/a
16	chr8:6189008-6189058	HIPEpiC	eye:	n/a
17	chr8:6189008-6189058	CMK	blood:	n/a
18	chr8:6189008-6189058	BE2_C	brain:	n/a
19	chr8:6189008-6189058	BJ	skin:	n/a
20	chr8:6189008-6189058	Caco-2	colon:	n/a
21	chr8:6189008-6189058	HAEpiC	amniotic membrane:	n/a
22	chr8:6189008-6189058	AG04450	lung:	fetal
23	chr8:6189008-6189058	HRCEpiC	kidney:	n/a
24	chr8:6189008-6189058	SKMC	muscle:	n/a
25	chr8:6189008-6189058	NHDF-neo	bronchial:	n/a
26	chr8:6189008-6189058	Hepatocyte	liver:	n/a
27	chr8:6189008-6189058	ovcar-3	ovarian:	n/a
28	chr8:6189008-6189058	NHBE	bronchial:	n/a
29	chr8:6189008-6189058	HCM	heart:	n/a
30	chr8:6189008-6189058	ProgFib	skin:	n/a
31	chr8:6189008-6189058	AG10803	skin:	n/a
32	chr8:6189008-6189058	GM12892	blood:	n/a
33	chr8:6189008-6189058	T-47D	breast:	n/a
34	chr8:6189008-6189058	MCF10A-Er-Src	breast:	n/a
35	chr8:6189008-6189058	RPTEC	kidney:	n/a
36	chr8:6189008-6189058	HNPCEpiC	eye:	n/a
37	chr8:6189008-6189058	HCF	heart:	n/a
38	chr8:6189008-6189058	A549	lung:	n/a
39	chr8:6189008-6189058	PANC-1	pancreas:	n/a
40	chr8:6189008-6189058	HUVEC	blood vessel:	n/a
41	chr8:6189008-6189058	IMR90	lung:	fetal
42	chr8:6189008-6189058	AG04449	skin:	fetal
43	chr8:6189008-6189058	HPAEpiC	pulmonary alveolar:	n/a
44	chr8:6189008-6189058	AoSMC	blood vessel:	n/a
45	chr8:6189008-6189058	NB4	blood:	n/a
46	chr8:6189008-6189058	U87	brain:	n/a
47	chr8:6189008-6189058	GM12891	blood:	n/a
48	chr8:6189008-6189058	HRE	kidney:	n/a
49	chr8:6189008-6189058	GM06990	blood:	n/a
50	chr8:6189008-6189058	AG09319	gingival:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:6178544..6180648-chr8:6180657..6183263,2	K562	blood:
2	chr8:6178544..6180648-chr8:6180657..6183263,2	K562	blood:
3	chr8:6145627..6147844-chr8:6162410..6164202,2	MCF-7	breast:
4	chr8:6245309..6247015-chr8:6262084..6263587,2	MCF-7	breast:
5	chr8:6221816..6223744-chr8:6224650..6226459,2	K562	blood:
6	chr8:6139049..6141857-chr8:6147372..6149538,2	K562	blood:
7	chr8:6245766..6247303-chr8:6249126..6250864,2	K562	blood:
8	chr8:6175216..6177017-chr8:6178392..6180174,2	K562	blood:
9	chr8:6115787..6116559-chr8:6229328..6229869,2	MCF-7	breast:
10	chr8:6139049..6141857-chr8:6147372..6149538,2	K562	blood:
11	chr8:6116111..6116635-chr8:6188825..6189362,2	MCF-7	breast:
12	chr8:6117190..6120021-chr8:6122326..6123985,2	K562	blood:
13	chr8:6117190..6120021-chr8:6122326..6123985,2	K562	blood:
14	chr8:6221816..6223744-chr8:6224650..6226459,2	K562	blood:
15	chr8:6145627..6147844-chr8:6162410..6164202,2	MCF-7	breast:
16	chr8:6245766..6247303-chr8:6249126..6250864,2	K562	blood:
17	chr8:6175216..6177017-chr8:6178392..6180174,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ANGPT2-8	chr8:6248485-6250049	ucscGeneNc_uc003wqf_1
2	lnc-ANGPT2-8	chr8:6250635-6251477	ucscGeneNc_uc003wqf_1

Variant related genes	Relation type
ENSG00000253880	TF binding region
ENSG00000253880	CpG island

Extended variants
information (count: 6255 )
Associated
traits (count: 146 )

Variant overlapped rSNPs/rCNVs (count:6255 , 50 per page) page: 1 2 3 4 5 6 7 ... 126

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13272289	chr8:6118630-6118631	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs191596840	chr8:6118632-6118633	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs73192604	chr8:6118641-6118642	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs551211803	chr8:6118642-6118643	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs571202359	chr8:6118646-6118647	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs144269519	chr8:6118649-6118650	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs148331163	chr8:6118662-6118663	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs79071082	chr8:6118663-6118664	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs12682045	chr8:6118677-6118678	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs141390996	chr8:6118680-6118681	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs573315018	chr8:6118687-6118688	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs542475281	chr8:6118688-6118689	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs13274647	chr8:6118694-6118695	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
14	rs79483788	chr8:6118717-6118718	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs533573261	chr8:6118743-6118744	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs575999896	chr8:6118744-6118745	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs183428192	chr8:6118757-6118758	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs563254690	chr8:6118764-6118765	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs150827950	chr8:6118777-6118778	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs573704682	chr8:6118781-6118782	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs139914889	chr8:6118786-6118787	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs188482830	chr8:6118849-6118850	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs117781146	chr8:6118864-6118865	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs377138067	chr8:6118867-6118868	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs145295729	chr8:6118887-6118888	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs80200786	chr8:6118894-6118895	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs117314838	chr8:6118914-6118915	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs550581727	chr8:6118919-6118920	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs527374641	chr8:6118922-6118923	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs567517480	chr8:6118924-6118925	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs541166465	chr8:6118936-6118937	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs147226620	chr8:6118957-6118958	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs532560149	chr8:6118967-6118968	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs539280229	chr8:6118973-6118974	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs55667317	chr8:6118975-6118976	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs569601821	chr8:6119008-6119009	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs538513217	chr8:6119038-6119039	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs556934405	chr8:6119039-6119040	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs200874071	chr8:6119100-6119101	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs201928657	chr8:6119106-6119107	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs66744999	chr8:6119108-6119109	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs202026191	chr8:6119109-6119110	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs199970449	chr8:6119111-6119112	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs142659543	chr8:6119119-6119120	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs71211473	chr8:6119127-6119128	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs59038985	chr8:6119130-6119131	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs529722054	chr8:6119141-6119142	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs547779641	chr8:6119142-6119143	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs566267004	chr8:6119194-6119195	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs568977482	chr8:6119199-6119200	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:146)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	16573809	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
abnormal development	18461090	CNVD
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
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
Epilepsy	22083797	CNVD
Acute myeloid leukemia	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Cancer	20164920	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Non-small cell lung cancer	21829676	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Prostate cancer	17217626	CNVD
Developmental delay	19128483	CNVD
Neuroticism	17667963	CNVD
Leukoplakia	24403051	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16774939	CNVD
Breast cancer	21364760	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Cancer	20164919	CNVD
Medulloblastoma	16783165	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Osteosarcoma	21215367	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
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
Schizophrenia	23813976	CNVD
Bladder cancer	21909424	CNVD
Autism	20685689	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:257 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:6119400-6120000	Enhancers	Brain Germinal Matrix	brain
2	chr8:6119400-6120000	Enhancers	Osteobl	bone
3	chr8:6119400-6120200	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr8:6120000-6121000	Weak transcription	Brain Germinal Matrix	brain
5	chr8:6120200-6120800	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr8:6120800-6121200	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr8:6121000-6121200	Enhancers	Brain Germinal Matrix	brain
8	chr8:6122200-6123200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr8:6128200-6128600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr8:6132000-6132800	Enhancers	Breast Myoepithelial Primary Cells	Breast
11	chr8:6132200-6132800	Enhancers	Spleen	Spleen
12	chr8:6132200-6133600	Enhancers	Pancreas	Pancrea
13	chr8:6132800-6134800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr8:6132800-6149000	Weak transcription	Spleen	Spleen
15	chr8:6134800-6135000	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr8:6138400-6141200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr8:6140200-6140400	Active TSS	Breast Myoepithelial Primary Cells	Breast
18	chr8:6140800-6141000	Active TSS	Breast Myoepithelial Primary Cells	Breast
19	chr8:6141200-6141400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr8:6141400-6144400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr8:6144400-6144600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr8:6144600-6147200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr8:6147200-6147400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr8:6147200-6148200	Enhancers	Breast Myoepithelial Primary Cells	Breast
25	chr8:6147200-6148200	Enhancers	Primary hematopoietic stem cells short term culture	blood
26	chr8:6147200-6148200	Enhancers	Monocytes-CD14+_RO01746	blood
27	chr8:6147200-6148600	Enhancers	Primary hematopoietic stem cells	blood
28	chr8:6147200-6148600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr8:6147200-6148600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr8:6147200-6148800	Enhancers	Primary monocytes fromperipheralblood	blood
31	chr8:6147600-6147800	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr8:6147800-6148000	Enhancers	Duodenum Mucosa	Duodenum
33	chr8:6147800-6148200	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr8:6147800-6148200	Enhancers	Adipose Nuclei	Adipose
35	chr8:6147800-6148200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
36	chr8:6147800-6148800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
37	chr8:6147800-6148800	Enhancers	Primary B cells from cord blood	blood
38	chr8:6148000-6149000	Enhancers	Primary B cells from peripheral blood	blood
39	chr8:6148000-6149000	Weak transcription	Duodenum Mucosa	Duodenum
40	chr8:6148200-6148600	Weak transcription	HUES48 Cell Line	embryonic stem cell
41	chr8:6148200-6149000	Enhancers	Primary neutrophils fromperipheralblood	blood
42	chr8:6148200-6149400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
43	chr8:6148200-6149600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
44	chr8:6148600-6149000	Enhancers	Brain Cingulate Gyrus	brain
45	chr8:6148600-6149400	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr8:6148600-6149400	Flanking Active TSS	Primary hematopoietic stem cells	blood
47	chr8:6148600-6149600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr8:6148600-6149800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr8:6148800-6149000	Bivalent/Poised TSS	Adipose Nuclei	Adipose
50	chr8:6148800-6149000	Enhancers	GM12878-XiMat	blood

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