Variant report

Variant	nsv539430
Chromosome Location	chr8:6109055-6253121
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	chr8:6132470-6132485	HepG2	liver:	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	chr8:6165750-6165958	HepG2	liver:	n/a	chr8:6165822-6165835 chr8:6165824-6165833 chr8:6165822-6165833
8	CEBPB	chr8:6165771-6165947	A549	lung:	n/a	chr8:6165822-6165835 chr8:6165824-6165833 chr8:6165822-6165833
9	CEBPB	chr8:6165750-6165950	IMR90	lung:	n/a	chr8:6165822-6165835 chr8:6165824-6165833 chr8:6165822-6165833
10	CEBPB	chr8:6200012-6200084	A549	lung:	n/a	n/a
11	CEBPB	chr8:6165763-6166327	K562	blood:	n/a	chr8:6165822-6165835 chr8:6165824-6165833 chr8:6165822-6165833
12	CEBPB	chr8:6128333-6128520	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr8:6229207-6229307	HepG2	liver:	n/a	chr8:6229236-6229247
14	CEBPB	chr8:6229961-6230353	A549	lung:	n/a	n/a
15	CEBPB	chr8:6128430-6128600	HepG2	liver:	n/a	n/a
16	CEBPB	chr8:6229956-6230363	HepG2	liver:	n/a	n/a
17	CEBPB	chr8:6230120-6230328	IMR90	lung:	n/a	n/a
18	CEBPB	chr8:6128437-6128476	K562	blood:	n/a	n/a
19	CEBPB	chr8:6231017-6231102	HepG2	liver:	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	chr8:6188860-6189010	GM12801	blood:	n/a	chr8:6188961-6188982 chr8:6188968-6188981 chr8:6188968-6188981 chr8:6188966-6188984
24	CTCF	chr8:6185400-6185550	WERI-Rb-1	eye:	n/a	chr8:6185537-6185550
25	CTCF	chr8:6188880-6189030	MCF-7	breast:	n/a	chr8:6188961-6188982 chr8:6188968-6188981 chr8:6188968-6188981 chr8:6188966-6188984
26	CTCF	chr8:6188880-6189030	GM12873	blood:	n/a	chr8:6188961-6188982 chr8:6188968-6188981 chr8:6188968-6188981 chr8:6188966-6188984
27	CTCF	chr8:6116100-6116250	WERI-Rb-1	eye:	n/a	n/a
28	CTCF	chr8:6232030-6232359	ECC-1	luminal epithelium:	n/a	chr8:6232214-6232235 chr8:6232220-6232236 chr8:6232224-6232232 chr8:6232221-6232234
29	CTCF	chr8:6188880-6189030	SK-N-SH_RA	brain:	n/a	chr8:6188961-6188982 chr8:6188968-6188981 chr8:6188968-6188981 chr8:6188966-6188984
30	CTCF	chr8:6232183-6232303	Spleen_OC	spleen:	n/a	chr8:6232214-6232235 chr8:6232220-6232236 chr8:6232224-6232232 chr8:6232221-6232234
31	CTCF	chr8:6232160-6232310	HBMEC	blood vessel:	n/a	chr8:6232214-6232235 chr8:6232220-6232236 chr8:6232224-6232232 chr8:6232221-6232234
32	CTCF	chr8:6140640-6140790	Caco-2	colon:	n/a	chr8:6140735-6140753 chr8:6140730-6140751
33	CTCF	chr8:6116160-6116310	SAEC	small airway:	n/a	n/a
34	CTCF	chr8:6232140-6232290	A549	lung:	n/a	chr8:6232214-6232235 chr8:6232220-6232236 chr8:6232224-6232232 chr8:6232221-6232234
35	CTCF	chr8:6116120-6116270	GM12878	blood:	n/a	n/a
36	CTCF	chr8:6188900-6189050	MCF-7	breast:	n/a	chr8:6188961-6188982 chr8:6188968-6188981 chr8:6188968-6188981 chr8:6188966-6188984
37	CTCF	chr8:6232200-6232350	K562	blood:	n/a	chr8:6232214-6232235 chr8:6232220-6232236 chr8:6232224-6232232 chr8:6232221-6232234
38	CTCF	chr8:6229740-6229890	Caco-2	colon:	n/a	n/a
39	CTCF	chr8:6188660-6188810	HAc	cerebellar:	n/a	n/a
40	CTCF	chr8:6140660-6140810	GM06990	blood:	n/a	chr8:6140735-6140753 chr8:6140730-6140751
41	CTCF	chr8:6229780-6229866	K562	blood:	n/a	n/a
42	CTCF	chr8:6232012-6232348	HepG2	liver:	n/a	chr8:6232214-6232235 chr8:6232220-6232236 chr8:6232224-6232232 chr8:6232221-6232234
43	CTCF	chr8:6232140-6232290	WERI-Rb-1	eye:	n/a	chr8:6232214-6232235 chr8:6232220-6232236 chr8:6232224-6232232 chr8:6232221-6232234
44	CTCF	chr8:6232120-6232270	GM12874	blood:	n/a	chr8:6232214-6232235 chr8:6232220-6232236 chr8:6232224-6232232 chr8:6232221-6232234
45	CTCF	chr8:6185477-6185623	Gliobla	brain:	n/a	chr8:6185537-6185550 chr8:6185536-6185552
46	CTCF	chr8:6188920-6189070	HCT-116	colon:	n/a	chr8:6188961-6188982 chr8:6188968-6188981 chr8:6188968-6188981 chr8:6188966-6188984
47	CTCF	chr8:6140672-6140825	GM12878	blood:	n/a	chr8:6140735-6140753 chr8:6140730-6140751
48	CTCF	chr8:6188860-6189010	WI-38	lung:	n/a	chr8:6188961-6188982 chr8:6188968-6188981 chr8:6188968-6188981 chr8:6188966-6188984
49	CTCF	chr8:6188818-6189082	H1-hESC	embryonic stem cell:	n/a	chr8:6188961-6188982 chr8:6188968-6188981 chr8:6188968-6188981 chr8:6188966-6188984
50	CTCF	chr8:6147121-6147372	K562	blood:	n/a	chr8:6147257-6147270

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:6118575-6118625	Caco-2	colon:	n/a
2	chr8:6189008-6189058	ECC-1	luminal epithelium:	n/a
3	chr8:6118575-6118625	BJ	skin:	n/a
4	chr8:6118575-6118625	GM12892	blood:	n/a
5	chr8:6118526-6118576	GM12892	blood:	n/a
6	chr8:6189008-6189058	IMR90	lung:	fetal
7	chr8:6118575-6118625	U87	brain:	n/a
8	chr8:6118575-6118625	CMK	blood:	n/a
9	chr8:6118575-6118625	HL-60	blood:	n/a
10	chr8:6118575-6118625	ovcar-3	ovarian:	n/a
11	chr8:6118526-6118576	HEK293	kidney:	embryo
12	chr8:6189008-6189058	HIPEpiC	eye:	n/a
13	chr8:6118526-6118576	CMK	blood:	n/a
14	chr8:6118575-6118625	HNPCEpiC	eye:	n/a
15	chr8:6118526-6118576	HAEpiC	amniotic membrane:	n/a
16	chr8:6118526-6118576	AG09319	gingival:	n/a
17	chr8:6189008-6189058	AG10803	skin:	n/a
18	chr8:6189008-6189058	HAEpiC	amniotic membrane:	n/a
19	chr8:6118526-6118576	BJ	skin:	n/a
20	chr8:6118526-6118576	Jurkat	blood:	n/a
21	chr8:6118575-6118625	PANC-1	pancreas:	n/a
22	chr8:6118575-6118625	NHBE	bronchial:	n/a
23	chr8:6118526-6118576	GM12878	blood:	n/a
24	chr8:6118526-6118576	LNCaP	prostate:	n/a
25	chr8:6118526-6118576	HCPEpiC	choroid plexus:	n/a
26	chr8:6189008-6189058	HMEC	breast:	n/a
27	chr8:6118526-6118576	T-47D	breast:	n/a
28	chr8:6189008-6189058	PrEC	prostate:	n/a
29	chr8:6118575-6118625	HRE	kidney:	n/a
30	chr8:6189008-6189058	T-47D	breast:	n/a
31	chr8:6118575-6118625	Jurkat	blood:	n/a
32	chr8:6118526-6118576	NHDF-neo	bronchial:	n/a
33	chr8:6189008-6189058	HRPEpiC	eye:	n/a
34	chr8:6118575-6118625	BE2_C	brain:	n/a
35	chr8:6118575-6118625	AG04450	lung:	fetal
36	chr8:6118575-6118625	T-47D	breast:	n/a
37	chr8:6118526-6118576	NB4	blood:	n/a
38	chr8:6118526-6118576	ProgFib	skin:	n/a
39	chr8:6118526-6118576	HCT-116	colon:	n/a
40	chr8:6118526-6118576	H1-hESC	embryonic stem cell:	embryo
41	chr8:6118526-6118576	GM12891	blood:	n/a
42	chr8:6118575-6118625	HRPEpiC	eye:	n/a
43	chr8:6118526-6118576	IMR90	lung:	fetal
44	chr8:6118526-6118576	K562	blood:	n/a
45	chr8:6118526-6118576	BE2_C	brain:	n/a
46	chr8:6118575-6118625	HCPEpiC	choroid plexus:	n/a
47	chr8:6189008-6189058	AG04449	skin:	fetal
48	chr8:6118526-6118576	HL-60	blood:	n/a
49	chr8:6189008-6189058	HPAEpiC	pulmonary alveolar:	n/a
50	chr8:6118575-6118625	HPAEpiC	pulmonary alveolar:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:6139049..6141857-chr8:6147372..6149538,2	K562	blood:
2	chr8:6116111..6116635-chr8:6188825..6189362,2	MCF-7	breast:
3	chr8:6221816..6223744-chr8:6224650..6226459,2	K562	blood:
4	chr8:6116111..6116635-chr8:6188825..6189362,2	MCF-7	breast:
5	chr8:6139049..6141857-chr8:6147372..6149538,2	K562	blood:
6	chr8:6175216..6177017-chr8:6178392..6180174,2	K562	blood:
7	chr8:6117190..6120021-chr8:6122326..6123985,2	K562	blood:
8	chr8:6245766..6247303-chr8:6249126..6250864,2	K562	blood:
9	chr8:6115678..6116241-chr8:6687345..6688278,2	K562	blood:
10	chr8:6145627..6147844-chr8:6162410..6164202,2	MCF-7	breast:
11	chr8:6115787..6116559-chr8:6229328..6229869,2	MCF-7	breast:
12	chr8:6117190..6120021-chr8:6122326..6123985,2	K562	blood:
13	chr8:6245309..6247015-chr8:6262084..6263587,2	MCF-7	breast:
14	chr8:6175216..6177017-chr8:6178392..6180174,2	K562	blood:
15	chr8:6178544..6180648-chr8:6180657..6183263,2	K562	blood:
16	chr8:6245766..6247303-chr8:6249126..6250864,2	K562	blood:
17	chr8:6115787..6116559-chr8:6229328..6229869,2	MCF-7	breast:
18	chr8:6178544..6180648-chr8:6180657..6183263,2	K562	blood:
19	chr8:6145627..6147844-chr8:6162410..6164202,2	MCF-7	breast:
20	chr8:6221816..6223744-chr8:6224650..6226459,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ANGPT2-3	chr8:6114933-6115058	ENSG00000253880
2	lnc-ANGPT2-8	chr8:6250635-6251477	ucscGeneNc_uc003wqf_1
3	lnc-ANGPT2-8	chr8:6248485-6250049	ucscGeneNc_uc003wqf_1

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

Extended variants
information (count: 7077 )
Associated
traits (count: 146 )

Variant overlapped rSNPs/rCNVs (count:7077 , 50 per page) page: 1 2 3 4 5 6 7 ... 142

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs548199538	chr8:6109057-6109058	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs376237669	chr8:6109074-6109075	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs571651821	chr8:6109084-6109085	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs527381524	chr8:6109109-6109110	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs146202740	chr8:6109129-6109130	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs55784936	chr8:6109132-6109133	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs570841222	chr8:6109136-6109137	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs59355288	chr8:6109141-6109142	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs78633334	chr8:6109142-6109143	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs570278313	chr8:6109172-6109173	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs536002840	chr8:6109192-6109193	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs79655605	chr8:6109195-6109196	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs572745529	chr8:6109198-6109199	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs535885631	chr8:6109201-6109202	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs55988315	chr8:6109214-6109215	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs553380662	chr8:6109237-6109238	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs576402457	chr8:6109240-6109241	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs183767747	chr8:6109264-6109265	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs60403285	chr8:6109269-6109270	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs545510780	chr8:6109285-6109286	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs578038196	chr8:6109286-6109287	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs78570840	chr8:6109297-6109298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs17076346	chr8:6109303-6109304	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs139224979	chr8:6109307-6109308	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs561727705	chr8:6109317-6109318	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs372672344	chr8:6109319-6109320	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs371931004	chr8:6109322-6109323	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs539381157	chr8:6109336-6109337	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs559188269	chr8:6109337-6109338	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs143957577	chr8:6109339-6109340	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs564492747	chr8:6109341-6109342	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs572726430	chr8:6109348-6109349	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs533329983	chr8:6109359-6109360	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs554509858	chr8:6109366-6109367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs550305707	chr8:6109380-6109381	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs188541406	chr8:6109381-6109382	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs34934178	chr8:6109403-6109404	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs56335709	chr8:6109405-6109406	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs566120813	chr8:6109407-6109408	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs79718124	chr8:6109429-6109430	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs117551263	chr8:6109443-6109444	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs576441207	chr8:6109468-6109469	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs376088576	chr8:6109470-6109471	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs181045209	chr8:6109477-6109478	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs139487326	chr8:6109484-6109485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs576129701	chr8:6109494-6109495	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs150021931	chr8:6109501-6109502	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs541542257	chr8:6109515-6109516	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs561945023	chr8:6109521-6109522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs184030955	chr8:6109529-6109530	Weak transcription Enhancers	n/a	n/a	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:273 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:6106400-6111200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr8:6106400-6111200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr8:6107400-6110200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr8:6107400-6110600	Weak transcription	Primary hematopoietic stem cells	blood
5	chr8:6110200-6110600	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr8:6110600-6111000	Enhancers	Primary hematopoietic stem cells	blood
7	chr8:6110600-6111800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr8:6111000-6112400	Weak transcription	Primary hematopoietic stem cells	blood
9	chr8:6111200-6112200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr8:6111200-6112200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr8:6111800-6112800	Enhancers	Primary hematopoietic stem cells short term culture	blood
12	chr8:6112200-6112600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr8:6112200-6112800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr8:6112400-6112600	Enhancers	Primary hematopoietic stem cells	blood
15	chr8:6112800-6114800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr8:6114800-6115200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr8:6114800-6115200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr8:6119400-6120000	Enhancers	Brain Germinal Matrix	brain
19	chr8:6119400-6120000	Enhancers	Osteobl	bone
20	chr8:6119400-6120200	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr8:6120000-6121000	Weak transcription	Brain Germinal Matrix	brain
22	chr8:6120200-6120800	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr8:6120800-6121200	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr8:6121000-6121200	Enhancers	Brain Germinal Matrix	brain
25	chr8:6122200-6123200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr8:6128200-6128600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr8:6132000-6132800	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr8:6132200-6132800	Enhancers	Spleen	Spleen
29	chr8:6132200-6133600	Enhancers	Pancreas	Pancrea
30	chr8:6132800-6134800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
31	chr8:6132800-6149000	Weak transcription	Spleen	Spleen
32	chr8:6134800-6135000	Enhancers	Breast Myoepithelial Primary Cells	Breast
33	chr8:6138400-6141200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr8:6140200-6140400	Active TSS	Breast Myoepithelial Primary Cells	Breast
35	chr8:6140800-6141000	Active TSS	Breast Myoepithelial Primary Cells	Breast
36	chr8:6141200-6141400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr8:6141400-6144400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr8:6144400-6144600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr8:6144600-6147200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr8:6147200-6147400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr8:6147200-6148200	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr8:6147200-6148200	Enhancers	Primary hematopoietic stem cells short term culture	blood
43	chr8:6147200-6148200	Enhancers	Monocytes-CD14+_RO01746	blood
44	chr8:6147200-6148600	Enhancers	Primary hematopoietic stem cells	blood
45	chr8:6147200-6148600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr8:6147200-6148600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr8:6147200-6148800	Enhancers	Primary monocytes fromperipheralblood	blood
48	chr8:6147600-6147800	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr8:6147800-6148000	Enhancers	Duodenum Mucosa	Duodenum
50	chr8:6147800-6148200	Enhancers	HUES48 Cell Line	embryonic stem cell

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