Variant report

Variant	nsv539414
Chromosome Location	chr8:5511172-5837654
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	chr8:5607668-5608196	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr8:5645898-5646187	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr8:5765727-5765858	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr8:5665134-5665329	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL11A	chr8:5532714-5533009	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr8:5633880-5633888	GM12878	blood:	n/a	n/a
7	BHLHE40	chr8:5833612-5833750	GM12878	blood:	n/a	n/a
8	BRCA1	chr8:5754693-5754799	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr8:5743115-5743330	H1-hESC	embryonic stem cell:	n/a	chr8:5743238-5743249 chr8:5743236-5743247 chr8:5743238-5743247 chr8:5743236-5743249
10	CEBPB	chr8:5532168-5532358	HepG2	liver:	n/a	chr8:5532275-5532288 chr8:5532276-5532287 chr8:5532275-5532286
11	CEBPB	chr8:5710994-5711190	HepG2	liver:	n/a	chr8:5711068-5711079
12	CEBPB	chr8:5649151-5649414	HepG2	liver:	n/a	n/a
13	CEBPB	chr8:5665500-5665846	A549	lung:	n/a	chr8:5665672-5665685 chr8:5665674-5665683 chr8:5665672-5665683 chr8:5665674-5665683 chr8:5665576-5665584 chr8:5665672-5665685 chr8:5665674-5665683 chr8:5665674-5665683 chr8:5665673-5665684
14	CEBPB	chr8:5731891-5732130	IMR90	lung:	n/a	chr8:5731971-5731982
15	CEBPB	chr8:5665491-5665861	HepG2	liver:	n/a	chr8:5665672-5665685 chr8:5665674-5665683 chr8:5665672-5665683 chr8:5665674-5665683 chr8:5665576-5665584 chr8:5665672-5665685 chr8:5665674-5665683 chr8:5665674-5665683 chr8:5665673-5665684
16	CEBPB	chr8:5743087-5743365	A549	lung:	n/a	chr8:5743238-5743249 chr8:5743236-5743247 chr8:5743238-5743247 chr8:5743236-5743249
17	CEBPB	chr8:5606425-5606513	A549	lung:	n/a	n/a
18	CEBPB	chr8:5513789-5514104	HepG2	liver:	n/a	chr8:5513934-5513945
19	CEBPB	chr8:5766581-5766595	A549	lung:	n/a	n/a
20	CEBPB	chr8:5743105-5743392	K562	blood:	n/a	chr8:5743238-5743249 chr8:5743236-5743247 chr8:5743238-5743247 chr8:5743236-5743249
21	CEBPB	chr8:5606430-5606630	HepG2	liver:	n/a	n/a
22	CEBPB	chr8:5750468-5750687	HepG2	liver:	n/a	n/a
23	CEBPB	chr8:5532924-5533107	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr8:5743074-5743414	IMR90	lung:	n/a	chr8:5743238-5743249 chr8:5743236-5743247 chr8:5743238-5743247 chr8:5743236-5743249
25	CEBPB	chr8:5665512-5665799	K562	blood:	n/a	chr8:5665672-5665685 chr8:5665674-5665683 chr8:5665672-5665683 chr8:5665674-5665683 chr8:5665576-5665584 chr8:5665672-5665685 chr8:5665674-5665683 chr8:5665674-5665683 chr8:5665673-5665684
26	CEBPB	chr8:5665505-5665860	IMR90	lung:	n/a	chr8:5665672-5665685 chr8:5665674-5665683 chr8:5665672-5665683 chr8:5665674-5665683 chr8:5665576-5665584 chr8:5665672-5665685 chr8:5665674-5665683 chr8:5665674-5665683 chr8:5665673-5665684
27	CEBPB	chr8:5584989-5585024	HepG2	liver:	n/a	chr8:5584999-5585010
28	CEBPB	chr8:5731799-5732146	HepG2	liver:	n/a	chr8:5731971-5731982
29	CEBPB	chr8:5572602-5572802	HepG2	liver:	n/a	chr8:5572684-5572695 chr8:5572683-5572694 chr8:5572683-5572696
30	CEBPB	chr8:5664965-5665044	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr8:5731829-5732132	H1-hESC	embryonic stem cell:	n/a	chr8:5731971-5731982
32	CEBPB	chr8:5665345-5665839	H1-hESC	embryonic stem cell:	n/a	chr8:5665672-5665685 chr8:5665674-5665683 chr8:5665672-5665683 chr8:5665674-5665683 chr8:5665576-5665584 chr8:5665672-5665685 chr8:5665674-5665683 chr8:5665674-5665683 chr8:5665673-5665684
33	CEBPB	chr8:5743077-5743413	HepG2	liver:	n/a	chr8:5743238-5743249 chr8:5743236-5743247 chr8:5743238-5743247 chr8:5743236-5743249
34	CEBPB	chr8:5731871-5732051	K562	blood:	n/a	chr8:5731971-5731982
35	CEBPB	chr8:5731815-5732103	A549	lung:	n/a	chr8:5731971-5731982
36	CHD2	chr8:5527476-5527834	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr8:5543363-5543413	Gliobla	brain:	n/a	n/a
38	CTCF	chr8:5741174-5741198	Lung_OC	lung:	n/a	n/a
39	CTCF	chr8:5657120-5657270	GM12873	blood:	n/a	n/a
40	CTCF	chr8:5828580-5828730	HFF-Myc	foreskin:	n/a	n/a
41	CTCF	chr8:5790174-5790455	GM12878	blood:	n/a	n/a
42	CTCF	chr8:5798340-5798490	HFF-Myc	foreskin:	n/a	n/a
43	CTCF	chr8:5790240-5790390	MCF-7	breast:	n/a	n/a
44	CTCF	chr8:5543620-5543770	BJ	skin:	n/a	chr8:5543674-5543692 chr8:5543676-5543697
45	CTCF	chr8:5798329-5798521	HepG2	liver:	n/a	n/a
46	CTCF	chr8:5828459-5828550	HepG2	liver:	n/a	n/a
47	CTCF	chr8:5828492-5828577	MCF-7	breast:	n/a	n/a
48	CTCF	chr8:5821241-5821292	Lung_OC	lung:	n/a	n/a
49	CTCF	chr8:5738260-5738330	GM10266	blood:	n/a	n/a
50	CTCF	chr8:5543520-5543670	NB4	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:5762990-5763040	AG09309	skin:	n/a
2	chr8:5762990-5763040	AG09309	skin:	n/a
3	chr8:5526092-5526142	Caco-2	colon:	n/a
4	chr8:5762990-5763040	HPAEpiC	pulmonary alveolar:	n/a
5	chr8:5762944-5762994	NT2-D1	testis:	n/a
6	chr8:5762990-5763040	RPTEC	kidney:	n/a
7	chr8:5762990-5763040	HAEpiC	amniotic membrane:	n/a
8	chr8:5526092-5526142	AoSMC	blood vessel:	n/a
9	chr8:5526092-5526142	H1-hESC	embryonic stem cell:	embryo
10	chr8:5526092-5526142	U87	brain:	n/a
11	chr8:5762944-5762994	NH-A	brain:	n/a
12	chr8:5762990-5763040	NT2-D1	testis:	n/a
13	chr8:5762944-5762994	HUVEC	blood vessel:	n/a
14	chr8:5526092-5526142	HIPEpiC	eye:	n/a
15	chr8:5762944-5762994	U87	brain:	n/a
16	chr8:5762944-5762994	HMEC	breast:	n/a
17	chr8:5762944-5762994	GM12892	blood:	n/a
18	chr8:5526092-5526142	PrEC	prostate:	n/a
19	chr8:5762944-5762994	RPTEC	kidney:	n/a
20	chr8:5762944-5762994	CMK	blood:	n/a
21	chr8:5526092-5526142	HNPCEpiC	eye:	n/a
22	chr8:5526092-5526142	HPAEpiC	pulmonary alveolar:	n/a
23	chr8:5762990-5763040	ovcar-3	ovarian:	n/a
24	chr8:5526092-5526142	HCF	heart:	n/a
25	chr8:5526092-5526142	AG09309	skin:	n/a
26	chr8:5762944-5762994	GM12891	blood:	n/a
27	chr8:5762944-5762994	HPAEpiC	pulmonary alveolar:	n/a
28	chr8:5762944-5762994	GM12878	blood:	n/a
29	chr8:5762944-5762994	HEK293	kidney:	embryo
30	chr8:5762990-5763040	HEEpiC	esophagus:	n/a
31	chr8:5762990-5763040	HEK293	kidney:	embryo
32	chr8:5762990-5763040	HCT-116	colon:	n/a
33	chr8:5762944-5762994	PFSK-1	brain:	n/a
34	chr8:5762990-5763040	HRPEpiC	eye:	n/a
35	chr8:5526092-5526142	LNCaP	prostate:	n/a
36	chr8:5526092-5526142	MCF10A-Er-Src	breast:	n/a
37	chr8:5762990-5763040	ProgFib	skin:	n/a
38	chr8:5526092-5526142	HRCEpiC	kidney:	n/a
39	chr8:5762944-5762994	HNPCEpiC	eye:	n/a
40	chr8:5762944-5762994	Caco-2	colon:	n/a
41	chr8:5762944-5762994	SAEC	small airway:	n/a
42	chr8:5762944-5762994	NHBE	bronchial:	n/a
43	chr8:5762944-5762994	HCM	heart:	n/a
44	chr8:5762990-5763040	Hela-S3	cervix:	n/a
45	chr8:5762990-5763040	NB4	blood:	n/a
46	chr8:5526092-5526142	Hela-S3	cervix:	n/a
47	chr8:5762990-5763040	IMR90	lung:	fetal
48	chr8:5762944-5762994	HRE	kidney:	n/a
49	chr8:5762944-5762994	IMR90	lung:	fetal
50	chr8:5526092-5526142	HUVEC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:5539160..5541154-chr8:5572222..5575011,2	K562	blood:
2	chr8:5535511..5537996-chr8:5538816..5540687,2	K562	blood:
3	chr8:5653098..5655133-chr8:5666888..5669291,2	MCF-7	breast:
4	chr4:47028381..47029208-chr8:5581216..5581723,2	MCF-7	breast:
5	chr8:5745375..5747333-chr8:5749537..5752235,2	K562	blood:
6	chr8:5658661..5661228-chr8:5666311..5668611,2	K562	blood:
7	chr8:5543604..5544126-chr8:5997197..5997756,2	MCF-7	breast:
8	chr8:5655115..5656724-chr8:5659683..5662268,2	K562	blood:
9	chr8:5653098..5655133-chr8:5666888..5669291,2	MCF-7	breast:
10	chr8:5775799..5778570-chr8:6262790..6264825,2	K562	blood:
11	chr8:5610821..5612324-chr8:5615595..5617703,2	K562	blood:
12	chr8:5658661..5661228-chr8:5666311..5668611,2	K562	blood:
13	chr8:5524220..5526546-chr8:5527520..5529311,2	K562	blood:
14	chr8:5655115..5656724-chr8:5659683..5662268,2	K562	blood:
15	chr8:5539160..5541154-chr8:5572222..5575011,2	K562	blood:
16	chr8:5707497..5710127-chr8:5711033..5712692,2	K562	blood:
17	chr8:5610821..5612324-chr8:5615595..5617703,2	K562	blood:
18	chr8:5707497..5710127-chr8:5711033..5712692,2	K562	blood:
19	chr8:5797855..5798416-chr8:5934095..5934883,2	MCF-7	breast:
20	chr8:5535511..5537996-chr8:5538816..5540687,2	K562	blood:
21	chr8:5745375..5747333-chr8:5749537..5752235,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ANGPT2-13	chr8:5703214-5703330	l_3534_chr8:5703213-5738710_testes
2	lnc-CSMD1-6	chr8:5522226-5522711	ENSG00000254007
3	lnc-CSMD1-6	chr8:5517201-5517508	ENSG00000254007
4	lnc-ANGPT2-6	chr8:5757144-5757253	XLOC_006982
5	lnc-ANGPT2-13	chr8:5738563-5738710	l_3534_chr8:5703213-5738710_testes
6	lnc-MCPH1-4	chr8:5706219-5707214	NONHSAT124761
7	lnc-CSMD1-6	chr8:5517279-5517508	XLOC_006981
8	lnc-CSMD1-6	chr8:5522226-5522285	XLOC_006981
9	lnc-ANGPT2-6	chr8:5715806-5715922	XLOC_006982
10	lnc-CSMD1-6	chr8:5527471-5527599	ENSG00000254007
11	lnc-ANGPT2-6	chr8:5751155-5751303	XLOC_006982
12	lnc-ANGPT2-12	chr8:5768467-5768758	NONHSAT124763

Variant related genes	Relation type
ENSG00000253571	TF binding region
ENSG00000254007	TF binding region
RN7SKP159	TF binding region
ENSG00000253571	CpG island
ENSG00000254007	CpG island
RN7SKP159	CpG island
ENSG00000147316	chromatin interactions
ENSG00000246089	chromatin interactions
ENSG00000254007	chromatin interactions
STRBP	miRNA target sites
STRADB	miRNA target sites

Extended variants
information (count: 8024 )
Associated
traits (count: 134 )

Variant overlapped rSNPs/rCNVs (count:8024 , 50 per page) page: 1 2 3 4 5 6 7 ... 161

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs527976560	chr8:5511172-5511173	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs7845109	chr8:5511179-5511180	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs138993131	chr8:5511182-5511183	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs141990419	chr8:5511186-5511187	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs7846143	chr8:5511201-5511202	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs568195308	chr8:5511236-5511237	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs535302523	chr8:5511253-5511254	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs78195932	chr8:5511256-5511257	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs565686819	chr8:5511279-5511280	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs539722909	chr8:5511291-5511292	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs10503315	chr8:5511301-5511302	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs148542129	chr8:5511323-5511324	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs536616769	chr8:5511336-5511337	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs10503316	chr8:5511345-5511346	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs551643449	chr8:5511427-5511428	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs555528316	chr8:5511430-5511431	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs4875607	chr8:5511450-5511451	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs141885527	chr8:5511460-5511461	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs150632261	chr8:5511461-5511462	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs572497299	chr8:5511470-5511471	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs546483624	chr8:5511488-5511489	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs73509777	chr8:5511489-5511490	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs538790565	chr8:5511491-5511492	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs114793944	chr8:5511501-5511502	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs561889521	chr8:5511511-5511512	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs35844461	chr8:5511515-5511516	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs68027294	chr8:5511518-5511519	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs529347238	chr8:5511542-5511543	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs577807076	chr8:5511544-5511545	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs547440318	chr8:5511558-5511559	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs139581190	chr8:5511561-5511562	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs539224703	chr8:5511567-5511568	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs551677923	chr8:5511570-5511571	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs569827755	chr8:5511575-5511576	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs537082636	chr8:5511577-5511578	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs144362844	chr8:5511591-5511592	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs573827019	chr8:5511607-5511608	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs377563705	chr8:5511621-5511622	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs62485070	chr8:5511632-5511633	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs553060984	chr8:5511641-5511642	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs375235029	chr8:5511646-5511647	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs572614647	chr8:5511659-5511660	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs546050166	chr8:5511674-5511675	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs147852987	chr8:5511675-5511676	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs188143050	chr8:5511677-5511678	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs543460770	chr8:5511687-5511688	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs573932572	chr8:5511694-5511695	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs62485071	chr8:5511724-5511725	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs529209448	chr8:5511744-5511745	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs547501326	chr8:5511745-5511746	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:134)

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
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16774939	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Chronic myeloid leukemia	21384125	CNVD
Tetralogy of Fallot	22912587	CNVD
Type 2 diabetes	21526130	CNVD
Medulloblastoma	16783165	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
early-passage human iPS cells	21368824	CNVD
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Medulloblastoma	21163964	CNVD
Obesity	21131291	CNVD
Schizophrenia	20967226	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Melanoma	20688739	CNVD

Chromatin state (count:291 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:5511000-5511800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr8:5514000-5514600	Enhancers	Fetal Muscle Leg	muscle
3	chr8:5518400-5518600	Enhancers	H9 Cell Line	embryonic stem cell
4	chr8:5518600-5522200	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr8:5518800-5519000	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr8:5521200-5521400	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr8:5522200-5522400	Enhancers	H9 Cell Line	embryonic stem cell
8	chr8:5522400-5525800	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr8:5522800-5523000	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr8:5523400-5525400	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr8:5524600-5526000	Enhancers	Fetal Brain Male	brain
12	chr8:5525000-5526600	Enhancers	Cortex derived primary cultured neurospheres	brain
13	chr8:5525400-5528000	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr8:5525400-5528200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr8:5525400-5528200	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr8:5525600-5526400	Enhancers	H1 Cell Line	embryonic stem cell
17	chr8:5525600-5528200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr8:5525800-5526000	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr8:5525800-5526000	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr8:5525800-5526000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr8:5525800-5528000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr8:5526000-5526200	Enhancers	H9 Cell Line	embryonic stem cell
23	chr8:5526000-5526200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr8:5526000-5527000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
25	chr8:5526000-5528800	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr8:5526200-5526400	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
27	chr8:5526200-5527200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr8:5526200-5527400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr8:5526400-5526600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr8:5526400-5527400	Weak transcription	H1 Cell Line	embryonic stem cell
31	chr8:5526600-5527000	Weak transcription	Cortex derived primary cultured neurospheres	brain
32	chr8:5526600-5527400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr8:5527000-5527800	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr8:5527000-5528000	Enhancers	Cortex derived primary cultured neurospheres	brain
35	chr8:5527200-5527400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr8:5527200-5527800	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr8:5527200-5527800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr8:5527400-5527800	Enhancers	H1 Cell Line	embryonic stem cell
39	chr8:5527400-5527800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr8:5527400-5528000	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr8:5527400-5528000	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr8:5527400-5528200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr8:5527400-5528200	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
44	chr8:5527800-5531400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
45	chr8:5527800-5532000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
46	chr8:5527800-5534400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr8:5528000-5532000	Weak transcription	HUES48 Cell Line	embryonic stem cell
48	chr8:5528000-5532400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
49	chr8:5528000-5532800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr8:5528000-5533200	Weak transcription	HUES6 Cell Line	embryonic stem cell

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