Variant report

Variant	esv8249
Chromosome Location	chr8:8675403-8683649
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	chr8:8683384-8683480	K562	blood:	n/a	n/a
2	ATF1	chr8:8683397-8683587	K562	blood:	n/a	n/a
3	CBX3	chr8:8678479-8678905	K562	blood:	n/a	n/a
4	CEBPB	chr8:8683234-8683588	K562	blood:	n/a	chr8:8683396-8683405 chr8:8683394-8683405 chr8:8683394-8683407
5	CEBPB	chr8:8683208-8683648	MCF-7	breast:	n/a	chr8:8683396-8683405 chr8:8683394-8683405 chr8:8683394-8683407
6	CEBPB	chr8:8683232-8683571	K562	blood:	n/a	chr8:8683396-8683405 chr8:8683394-8683405 chr8:8683394-8683407
7	CEBPB	chr8:8683283-8683520	K562	blood:	n/a	chr8:8683396-8683405 chr8:8683394-8683405 chr8:8683394-8683407
8	CEBPB	chr8:8683324-8683546	IMR90	lung:	n/a	chr8:8683396-8683405 chr8:8683394-8683405 chr8:8683394-8683407
9	CEBPB	chr8:8679341-8679360	IMR90	lung:	n/a	n/a
10	CTCF	chr8:8679577-8679697	GM19238	blood:	n/a	n/a
11	CTCF	chr8:8679600-8679750	GM12867	blood:	n/a	n/a
12	CTCF	chr8:8679460-8679610	BE2_C	brain:	n/a	n/a
13	CTCF	chr8:8679700-8679850	GM12872	blood:	n/a	n/a
14	CTCF	chr8:8679533-8679707	GM19239	blood:	n/a	n/a
15	EBF1	chr8:8679509-8679876	GM12878	blood:	n/a	chr8:8679699-8679708 chr8:8679698-8679709 chr8:8679699-8679708 chr8:8679697-8679710
16	EBF1	chr8:8679490-8679804	GM12878	blood:	n/a	chr8:8679699-8679708 chr8:8679698-8679709 chr8:8679699-8679708 chr8:8679697-8679710
17	EBF1	chr8:8679665-8679873	GM12878	blood:	n/a	chr8:8679699-8679708 chr8:8679698-8679709 chr8:8679699-8679708 chr8:8679697-8679710
18	EP300	chr8:8683362-8683606	K562	blood:	n/a	n/a
19	FOS	chr8:8683220-8683796	HUVEC	blood vessel:	n/a	n/a
20	GATA2	chr8:8683063-8683819	HUVEC	blood vessel:	n/a	chr8:8683627-8683637 chr8:8683361-8683368
21	GATA2	chr8:8681939-8682528	SH-SY5Y	brain:	n/a	n/a
22	GATA2	chr8:8679228-8679593	SH-SY5Y	brain:	n/a	n/a
23	GATA3	chr8:8681977-8682534	SK-N-SH	brain:	n/a	n/a
24	GATA3	chr8:8681992-8682336	SH-SY5Y	brain:	n/a	n/a
25	GATA3	chr8:8683322-8683671	MCF-7	breast:	n/a	chr8:8683627-8683637 chr8:8683361-8683368
26	GTF2F1	chr8:8678785-8678856	H1-hESC	embryonic stem cell:	n/a	n/a
27	IRF1	chr8:8683399-8683696	K562	blood:	n/a	n/a
28	IRF1	chr8:8676417-8676440	K562	blood:	n/a	n/a
29	JUN	chr8:8683391-8683668	HUVEC	blood vessel:	n/a	n/a
30	JUND	chr8:8678431-8678577	K562	blood:	n/a	chr8:8678543-8678551 chr8:8678541-8678553
31	JUND	chr8:8683369-8683531	K562	blood:	n/a	n/a
32	NR2F2	chr8:8683279-8683573	K562	blood:	n/a	n/a
33	POLR2A	chr8:8682680-8682847	K562	blood:	n/a	n/a
34	POLR2A	chr8:8683220-8683809	HUVEC	blood vessel:	n/a	n/a
35	POLR2A	chr8:8678710-8678779	H1-hESC	embryonic stem cell:	n/a	n/a
36	POLR2A	chr8:8681145-8681597	H1-neurons	neurons:	n/a	n/a
37	POLR2A	chr8:8682365-8682410	MCF-7	breast:	n/a	n/a
38	POLR2A	chr8:8677560-8677976	K562	blood:	n/a	n/a
39	POLR2A	chr8:8678104-8678132	Hela-S3	cervix:	n/a	n/a
40	POLR2A	chr8:8683305-8683706	HUVEC	blood vessel:	n/a	n/a
41	RCOR1	chr8:8683315-8683619	K562	blood:	n/a	n/a
42	SPI1	chr8:8678443-8678643	K562	blood:	n/a	chr8:8678550-8678563 chr8:8678578-8678587 chr8:8678599-8678612
43	SPI1	chr8:8680963-8681318	HL-60	blood:	n/a	n/a
44	TBL1XR1	chr8:8683328-8683566	K562	blood:	n/a	n/a
45	UBTF	chr8:8683464-8683568	K562	blood:	n/a	n/a
46	ZBTB7A	chr8:8678508-8678722	K562	blood:	n/a	n/a
47	ZNF143	chr8:8678532-8678871	H1-hESC	embryonic stem cell:	n/a	n/a
48	ZNF143	chr8:8678648-8678745	K562	blood:	n/a	n/a
49	ZNF143	chr8:8676178-8676195	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:8680903-8680953	PANC-1	pancreas:	n/a
2	chr8:8680971-8681021	HCPEpiC	choroid plexus:	n/a
3	chr8:8681198-8681248	AG10803	skin:	n/a
4	chr8:8680903-8680953	AG04449	skin:	fetal
5	chr8:8681339-8681389	HAEpiC	amniotic membrane:	n/a
6	chr8:8680971-8681021	HRE	kidney:	n/a
7	chr8:8679450-8679500	NT2-D1	testis:	n/a
8	chr8:8679450-8679500	LNCaP	prostate:	n/a
9	chr8:8681198-8681248	GM12878	blood:	n/a
10	chr8:8681198-8681248	NHBE	bronchial:	n/a
11	chr8:8681339-8681389	PANC-1	pancreas:	n/a
12	chr8:8681339-8681389	HepG2	liver:	n/a
13	chr8:8680924-8680974	CMK	blood:	n/a
14	chr8:8680903-8680953	SKMC	muscle:	n/a
15	chr8:8680924-8680974	T-47D	breast:	n/a
16	chr8:8679450-8679500	K562	blood:	n/a
17	chr8:8679450-8679500	GM12878	blood:	n/a
18	chr8:8679450-8679500	SAEC	small airway:	n/a
19	chr8:8681339-8681389	MCF10A-Er-Src	breast:	n/a
20	chr8:8681198-8681248	U87	brain:	n/a
21	chr8:8680924-8680974	NB4	blood:	n/a
22	chr8:8680903-8680953	A549	lung:	n/a
23	chr8:8680924-8680974	SK-N-SH_RA	brain:	n/a
24	chr8:8680924-8680974	Hepatocyte	liver:	n/a
25	chr8:8680903-8680953	T-47D	breast:	n/a
26	chr8:8680971-8681021	RPTEC	kidney:	n/a
27	chr8:8680971-8681021	SK-N-MC	brain:	n/a
28	chr8:8680924-8680974	AG10803	skin:	n/a
29	chr8:8679450-8679500	SKMC	muscle:	n/a
30	chr8:8681339-8681389	SAEC	small airway:	n/a
31	chr8:8681339-8681389	HCT-116	colon:	n/a
32	chr8:8680903-8680953	PrEC	prostate:	n/a
33	chr8:8680903-8680953	H1-hESC	embryonic stem cell:	embryo
34	chr8:8680971-8681021	HUVEC	blood vessel:	n/a
35	chr8:8680903-8680953	IMR90	lung:	fetal
36	chr8:8680971-8681021	SAEC	small airway:	n/a
37	chr8:8681339-8681389	HCM	heart:	n/a
38	chr8:8680971-8681021	ProgFib	skin:	n/a
39	chr8:8680971-8681021	HCT-116	colon:	n/a
40	chr8:8681198-8681248	NH-A	brain:	n/a
41	chr8:8680924-8680974	HRE	kidney:	n/a
42	chr8:8680924-8680974	AG04450	lung:	fetal
43	chr8:8680924-8680974	HCF	heart:	n/a
44	chr8:8680903-8680953	BE2_C	brain:	n/a
45	chr8:8680903-8680953	HCT-116	colon:	n/a
46	chr8:8681198-8681248	HUVEC	blood vessel:	n/a
47	chr8:8680903-8680953	HCM	heart:	n/a
48	chr8:8681339-8681389	CMK	blood:	n/a
49	chr8:8680924-8680974	LNCaP	prostate:	n/a
50	chr8:8681339-8681389	SK-N-SH	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:8680684..8683788-chr8:8684972..8687852,3	K562	blood:
2	chr8:8678976..8682016-chr8:8748981..8752043,3	MCF-7	breast:
3	chr8:8676467..8679551-chr8:8749550..8751180,3	K562	blood:
4	chr8:8674703..8676330-chr8:8678081..8680231,2	K562	blood:

Variant related genes	Relation type
MFHAS1	TF binding region
MFHAS1	CpG island
ENSG00000147324	chromatin interactions

Extended variants
information (count: 489 )
Associated
traits (count: 140 )

Variant overlapped rSNPs/rCNVs (count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566119650	chr8:8675403-8675404	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs528601250	chr8:8675410-8675411	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs551526700	chr8:8675452-8675453	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs571492379	chr8:8675453-8675454	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs55961293	chr8:8675478-8675479	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs55657655	chr8:8675491-8675492	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs567627639	chr8:8675505-8675506	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs372070247	chr8:8675506-8675507	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs536196490	chr8:8675544-8675545	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs186996953	chr8:8675591-8675592	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs149785191	chr8:8675592-8675593	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs74751801	chr8:8675606-8675607	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs558711844	chr8:8675639-8675640	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs139448908	chr8:8675676-8675677	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs143020775	chr8:8675689-8675690	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs144138770	chr8:8675696-8675697	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs543095541	chr8:8675706-8675707	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs386722008	chr8:8675712-8675713	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs202023853	chr8:8675714-8675715	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs192281901	chr8:8675750-8675751	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs529951221	chr8:8675800-8675801	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs182249799	chr8:8675801-8675802	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs74453389	chr8:8675816-8675817	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs528522461	chr8:8675833-8675834	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs367968950	chr8:8675835-8675836	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs186874742	chr8:8675911-8675912	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs375816414	chr8:8675948-8675949	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs551440369	chr8:8675985-8675986	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs149089927	chr8:8676014-8676015	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs77138270	chr8:8676043-8676044	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs190584719	chr8:8676069-8676070	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs111277478	chr8:8676080-8676081	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs116866654	chr8:8676150-8676151	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs143110727	chr8:8676165-8676166	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs187038022	chr8:8676170-8676171	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs370842607	chr8:8676192-8676193	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs151170024	chr8:8676203-8676204	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs140193041	chr8:8676204-8676205	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs146941266	chr8:8676241-8676242	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs544377516	chr8:8676281-8676282	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs554827488	chr8:8676322-8676323	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs11986429	chr8:8676328-8676329	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs540141431	chr8:8676331-8676332	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs56765590	chr8:8676360-8676361	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs386722009	chr8:8676368-8676369	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs528473568	chr8:8676369-8676370	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs143342312	chr8:8676382-8676383	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs147119329	chr8:8676468-8676469	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs530933411	chr8:8676488-8676489	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs59312159	chr8:8676490-8676491	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:140)

Disease	PMID	Source
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
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
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
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
Colorectal cancer	16774939	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
Bladder cancer	21909424	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
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Bipolar disorder	19114987	CNVD
Gastric cancer	17229543	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:239 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:8637600-8679800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr8:8655200-8680600	Weak transcription	Colonic Mucosa	Colon
3	chr8:8655600-8685600	Weak transcription	Fetal Brain Female	brain
4	chr8:8658400-8687200	Weak transcription	Skeletal Muscle Male	skeletal muscle
5	chr8:8660200-8684400	Weak transcription	HSMMtube	muscle
6	chr8:8662600-8683400	Weak transcription	Rectal Mucosa Donor 31	rectum
7	chr8:8662800-8679800	Weak transcription	Brain Angular Gyrus	brain
8	chr8:8663400-8691800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr8:8663600-8681400	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr8:8664000-8678600	Weak transcription	Spleen	Spleen
11	chr8:8664000-8682400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr8:8664200-8681200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr8:8664200-8691400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr8:8664400-8691800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr8:8664600-8683200	Weak transcription	Muscle Satellite Cultured Cells	--
16	chr8:8667000-8680000	Weak transcription	Esophagus	oesophagus
17	chr8:8667200-8678400	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr8:8667200-8683600	Weak transcription	NHDF-Ad	bronchial
19	chr8:8667200-8685800	Weak transcription	Right Atrium	heart
20	chr8:8667200-8686200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr8:8667200-8699200	Weak transcription	Aorta	Aorta
22	chr8:8667200-8701600	Weak transcription	Sigmoid Colon	Sigmoid Colon
23	chr8:8667400-8677800	Weak transcription	Fetal Muscle Leg	muscle
24	chr8:8667400-8678200	Weak transcription	Adipose Nuclei	Adipose
25	chr8:8667400-8678400	Weak transcription	A549	lung
26	chr8:8667400-8679000	Weak transcription	NHLF	lung
27	chr8:8667400-8685400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr8:8667400-8686000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr8:8667400-8693400	Weak transcription	Small Intestine	intestine
30	chr8:8667600-8679200	Weak transcription	HepG2	liver
31	chr8:8667600-8679400	Weak transcription	H1 Cell Line	embryonic stem cell
32	chr8:8667600-8679800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr8:8667600-8685800	Weak transcription	HUES48 Cell Line	embryonic stem cell
34	chr8:8667600-8701000	Weak transcription	HUES64 Cell Line	embryonic stem cell
35	chr8:8668200-8681400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
36	chr8:8668600-8679400	Weak transcription	Fetal Brain Male	brain
37	chr8:8668600-8679800	Weak transcription	Fetal Kidney	kidney
38	chr8:8669800-8677200	Weak transcription	Primary monocytes fromperipheralblood	blood
39	chr8:8670000-8676400	Weak transcription	Monocytes-CD14+_RO01746	blood
40	chr8:8670000-8677800	Weak transcription	Fetal Lung	lung
41	chr8:8670000-8678200	Weak transcription	Fetal Intestine Small	intestine
42	chr8:8670000-8679400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr8:8670000-8701200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr8:8670200-8678000	Weak transcription	Fetal Thymus	thymus
45	chr8:8670200-8678200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr8:8670200-8678200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr8:8670200-8678600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr8:8670200-8682800	Weak transcription	Fetal Intestine Large	intestine
49	chr8:8670200-8701200	Weak transcription	Duodenum Mucosa	Duodenum
50	chr8:8670400-8677800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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