Variant report

Variant	esv3324025
Chromosome Location	chr8:131439370-131443168
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	chr8:131438707-131439423	HepG2	liver:	n/a	n/a
2	CEBPB	chr8:131438949-131439386	HepG2	liver:	n/a	n/a
3	CTCF	chr8:131440834-131440943	GM19239	blood:	n/a	n/a
4	CTCF	chr8:131440902-131440981	NHEK	skin:	n/a	n/a
5	CTCF	chr8:131442120-131442270	AG09319	gingival:	n/a	n/a
6	E2F4	chr8:131442020-131442278	MCF10A-Er-Src	breast:	n/a	n/a
7	EP300	chr8:131438990-131439383	HepG2	liver:	n/a	n/a
8	ESR1	chr8:131442022-131442421	T-47D	breast:	n/a	chr8:131442197-131442214
9	ESR1	chr8:131441996-131442321	T-47D	breast:	n/a	chr8:131442197-131442214
10	ESR1	chr8:131441992-131442406	T-47D	breast:	n/a	chr8:131442197-131442214
11	FOS	chr8:131441941-131442313	MCF10A-Er-Src	breast:	n/a	chr8:131442086-131442098
12	FOS	chr8:131440193-131440467	HUVEC	blood vessel:	n/a	chr8:131440324-131440335 chr8:131440327-131440338 chr8:131440324-131440336 chr8:131440325-131440334 chr8:131440325-131440335
13	FOS	chr8:131441935-131442345	MCF10A-Er-Src	breast:	n/a	chr8:131442086-131442098
14	FOS	chr8:131440216-131440464	MCF10A-Er-Src	breast:	n/a	chr8:131440324-131440335 chr8:131440327-131440338 chr8:131440324-131440336 chr8:131440325-131440334 chr8:131440325-131440335
15	FOS	chr8:131440195-131440466	MCF10A-Er-Src	breast:	n/a	chr8:131440324-131440335 chr8:131440327-131440338 chr8:131440324-131440336 chr8:131440325-131440334 chr8:131440325-131440335
16	FOS	chr8:131441939-131442342	MCF10A-Er-Src	breast:	n/a	chr8:131442086-131442098
17	FOS	chr8:131441926-131442345	MCF10A-Er-Src	breast:	n/a	chr8:131442086-131442098
18	FOS	chr8:131440174-131440520	MCF10A-Er-Src	breast:	n/a	chr8:131440324-131440335 chr8:131440327-131440338 chr8:131440324-131440336 chr8:131440325-131440334 chr8:131440325-131440335
19	FOS	chr8:131440236-131440466	MCF10A-Er-Src	breast:	n/a	chr8:131440324-131440335 chr8:131440327-131440338 chr8:131440324-131440336 chr8:131440325-131440334 chr8:131440325-131440335
20	FOSL2	chr8:131440106-131440559	A549	lung:	n/a	chr8:131440327-131440338 chr8:131440324-131440336 chr8:131440325-131440334 chr8:131440325-131440335
21	FOXA1	chr8:131438864-131439711	HepG2	liver:	n/a	n/a
22	FOXA1	chr8:131438800-131439411	HepG2	liver:	n/a	n/a
23	FOXA1	chr8:131438853-131439472	HepG2	liver:	n/a	n/a
24	FOXA2	chr8:131438788-131439711	HepG2	liver:	n/a	n/a
25	FOXA2	chr8:131439462-131439736	HepG2	liver:	n/a	n/a
26	FOXA2	chr8:131438892-131439397	HepG2	liver:	n/a	n/a
27	GABPA	chr8:131443021-131443458	A549	lung:	n/a	n/a
28	GATA3	chr8:131441711-131442411	T-47D	breast:	n/a	n/a
29	GATA3	chr8:131441658-131442319	T-47D	breast:	n/a	n/a
30	HDAC2	chr8:131438850-131439436	HepG2	liver:	n/a	n/a
31	JUND	chr8:131439004-131439387	HepG2	liver:	n/a	n/a
32	JUND	chr8:131440176-131440512	HepG2	liver:	n/a	chr8:131440327-131440338 chr8:131440324-131440335 chr8:131440324-131440336 chr8:131440325-131440334 chr8:131440325-131440335
33	MAX	chr8:131438606-131439445	HepG2	liver:	n/a	n/a
34	MXI1	chr8:131438721-131439436	IMR90	lung:	n/a	n/a
35	MXI1	chr8:131438813-131439543	HepG2	liver:	n/a	n/a
36	MYBL2	chr8:131438884-131439387	HepG2	liver:	n/a	n/a
37	MYC	chr8:131440807-131440811	MCF-7	breast:	n/a	n/a
38	MYC	chr8:131440819-131440836	MCF-7	breast:	n/a	n/a
39	MYC	chr8:131441870-131442345	MCF10A-Er-Src	breast:	n/a	chr8:131442109-131442118
40	MYC	chr8:131440604-131440714	MCF-7	breast:	n/a	n/a
41	MYC	chr8:131440786-131440793	MCF-7	breast:	n/a	n/a
42	MYC	chr8:131440595-131440814	MCF-7	breast:	n/a	n/a
43	MYC	chr8:131440751-131440785	MCF-7	breast:	n/a	n/a
44	MYC	chr8:131441941-131442344	MCF10A-Er-Src	breast:	n/a	chr8:131442109-131442118
45	NFIC	chr8:131438881-131439400	HepG2	liver:	n/a	n/a
46	POLR2A	chr8:131440813-131440903	HepG2	liver:	n/a	n/a
47	POLR2A	chr8:131442169-131442292	MCF10A-Er-Src	breast:	n/a	n/a
48	POLR2A	chr8:131440791-131440809	Gliobla	brain:	n/a	n/a
49	POLR2A	chr8:131440757-131440777	Gliobla	brain:	n/a	n/a
50	POLR2A	chr8:131442996-131443778	A549	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:131439812-131439862	HCPEpiC	choroid plexus:	n/a
2	chr8:131440305-131440355	NT2-D1	testis:	n/a
3	chr8:131441413-131441463	K562	blood:	n/a
4	chr8:131441413-131441463	NHDF-neo	bronchial:	n/a
5	chr8:131440305-131440355	SK-N-SH_RA	brain:	n/a
6	chr8:131439812-131439862	IMR90	lung:	fetal
7	chr8:131441413-131441463	HepG2	liver:	n/a
8	chr8:131439812-131439862	AG09319	gingival:	n/a
9	chr8:131440305-131440355	HRPEpiC	eye:	n/a
10	chr8:131441413-131441463	T-47D	breast:	n/a
11	chr8:131439812-131439862	NH-A	brain:	n/a
12	chr8:131441413-131441463	SK-N-SH_RA	brain:	n/a
13	chr8:131440305-131440355	ProgFib	skin:	n/a
14	chr8:131440305-131440355	T-47D	breast:	n/a
15	chr8:131439812-131439862	CMK	blood:	n/a
16	chr8:131441413-131441463	HEK293	kidney:	embryo
17	chr8:131440305-131440355	AG04450	lung:	fetal
18	chr8:131439812-131439862	HAEpiC	amniotic membrane:	n/a
19	chr8:131440305-131440355	NHDF-neo	bronchial:	n/a
20	chr8:131441413-131441463	Caco-2	colon:	n/a
21	chr8:131439812-131439862	HRE	kidney:	n/a
22	chr8:131440305-131440355	GM12878	blood:	n/a
23	chr8:131441413-131441463	HUVEC	blood vessel:	n/a
24	chr8:131439812-131439862	MCF-7	breast:	n/a
25	chr8:131439812-131439862	Hepatocyte	liver:	n/a
26	chr8:131440305-131440355	AoSMC	blood vessel:	n/a
27	chr8:131440305-131440355	LNCaP	prostate:	n/a
28	chr8:131439812-131439862	HEEpiC	esophagus:	n/a
29	chr8:131441413-131441463	ECC-1	luminal epithelium:	n/a
30	chr8:131441413-131441463	HPAEpiC	pulmonary alveolar:	n/a
31	chr8:131441413-131441463	AG09319	gingival:	n/a
32	chr8:131440305-131440355	AG09319	gingival:	n/a
33	chr8:131439812-131439862	AoSMC	blood vessel:	n/a
34	chr8:131441413-131441463	NH-A	brain:	n/a
35	chr8:131440305-131440355	GM12891	blood:	n/a
36	chr8:131441413-131441463	NT2-D1	testis:	n/a
37	chr8:131440305-131440355	SKMC	muscle:	n/a
38	chr8:131440305-131440355	PANC-1	pancreas:	n/a
39	chr8:131441413-131441463	HRCEpiC	kidney:	n/a
40	chr8:131439812-131439862	HCF	heart:	n/a
41	chr8:131440305-131440355	HIPEpiC	eye:	n/a
42	chr8:131441413-131441463	Jurkat	blood:	n/a
43	chr8:131441413-131441463	Hepatocyte	liver:	n/a
44	chr8:131440305-131440355	Caco-2	colon:	n/a
45	chr8:131441413-131441463	AoSMC	blood vessel:	n/a
46	chr8:131439812-131439862	AG09309	skin:	n/a
47	chr8:131440305-131440355	HEEpiC	esophagus:	n/a
48	chr8:131441413-131441463	IMR90	lung:	fetal
49	chr8:131440305-131440355	HAEpiC	amniotic membrane:	n/a
50	chr8:131441413-131441463	HCF	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:131436507..131441847-chr8:131454010..131456873,7	MCF-7	breast:
2	chr8:131441459..131443636-chr8:131445223..131447112,2	K562	blood:
3	chr8:131442808..131445703-chr8:131454691..131456819,2	MCF-7	breast:
4	chr8:131442195..131445335-chr8:131452635..131456457,4	MCF-7	breast:
5	chr8:131442973..131445344-chr8:131451202..131452908,2	MCF-7	breast:

Variant related genes	Relation type
ASAP1	TF binding region
ASAP1	CpG island
ENSG00000153317	chromatin interactions

Extended variants
information (count: 161 )
Associated
traits (count: 156 )

Variant overlapped rSNPs/rCNVs (count:161 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535184358	chr8:131439394-131439395	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs547443406	chr8:131439395-131439396	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs565675533	chr8:131439469-131439470	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs191208865	chr8:131439496-131439497	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs540176411	chr8:131439524-131439525	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs183420418	chr8:131439528-131439529	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs187958635	chr8:131439582-131439583	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs193180599	chr8:131439586-131439587	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs555593106	chr8:131439607-131439608	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs557863226	chr8:131439626-131439627	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs146457316	chr8:131439674-131439675	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs541165037	chr8:131439676-131439677	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs559364127	chr8:131439677-131439678	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs577577348	chr8:131439691-131439692	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs545694991	chr8:131439694-131439695	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs11775398	chr8:131439767-131439768	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs74724856	chr8:131439805-131439806	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs73711702	chr8:131439852-131439853	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs561709607	chr8:131439856-131439857	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs529030124	chr8:131440032-131440033	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs547506129	chr8:131440074-131440075	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs75191282	chr8:131440087-131440088	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs184276371	chr8:131440109-131440110	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs552121846	chr8:131440224-131440225	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs545700889	chr8:131440265-131440266	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs140698505	chr8:131440306-131440307	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs537327237	chr8:131440315-131440316	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs555974812	chr8:131440336-131440337	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs187812735	chr8:131440347-131440348	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs150101048	chr8:131440359-131440360	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs72726220	chr8:131440374-131440375	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs13272567	chr8:131440409-131440410	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs577640749	chr8:131440436-131440437	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs13272817	chr8:131440447-131440448	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs13272819	chr8:131440449-131440450	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs529515875	chr8:131440456-131440457	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs192382290	chr8:131440477-131440478	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs556923444	chr8:131440495-131440496	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs13273116	chr8:131440573-131440574	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs183630500	chr8:131440584-131440585	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs117879295	chr8:131440596-131440597	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs561956844	chr8:131440619-131440620	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs529035825	chr8:131440631-131440632	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs200348638	chr8:131440656-131440657	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs76514441	chr8:131440666-131440667	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs78805487	chr8:131440667-131440668	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs368757728	chr8:131440676-131440677	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs370574684	chr8:131440680-131440681	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs79814615	chr8:131440688-131440689	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs77801024	chr8:131440691-131440692	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:156)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	17603634	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	20729466	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Gastric cancer	21528007	CNVD
Breast cancer	22532251	CNVD
Cervical cancer	21062161	CNVD
Cancer	21129771	CNVD
benign familial neonatal convulsions	18472482	CNVD
Breast cancer	16417655	CNVD
Astrocytoma	17387387	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	20814816	CNVD
Colorectal cancer	22486879	CNVD
Breast cancer	17908964	CNVD
Colorectal cancer	20031965	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian cancer	17908964	CNVD
Ovarian cancer	20031965	CNVD
Prostate cancer	20031965	CNVD
Non-small cell lung cancer	17643093	CNVD
Prostate cancer	19242612	CNVD
Colorectal cancer	16774939	CNVD
Malignant melanoma	17260012	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute myeloid leukemia	18379011	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	22048815	CNVD
Colorectal cancer	16912164	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Lung adenocarcinoma	21148746	CNVD
Lung cancer	21911935	CNVD
Breast cancer	20459607	CNVD
Medulloblastoma	19270706	CNVD
Acute myeloid leukemia	19651601	CNVD
Colorectal cancer	21645411	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Colorectal cancer	19455253	CNVD
Glioblastoma multiforme	22286061	CNVD
Colorectal cancer	22860045	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Lung cancer	17925434	CNVD
Non-small cell lung cancer	21829676	CNVD
Prostate cancer	17217626	CNVD
Cancer	17160897	CNVD
Breast cancer	16497871	CNVD
Colorectal cancer	16882699	CNVD
Cystic fibrosis	19273617	CNVD
Chronic stroke	19622162	CNVD
Chordoma	18071362	CNVD
Breast cancer	17850661	CNVD
head and neck squamous cell carcinoma	16740747	CNVD
Gastric cancer	22539939	CNVD
Breast cancer	16272173	CNVD
Uveal melanoma	20484589	CNVD
Ovarian cancer	20844748	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21611746	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Gastrointestinal stromal cancer	20818650	CNVD

Chromatin state (count:169 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:131417000-131440600	Weak transcription	Fetal Kidney	kidney
2	chr8:131429000-131446800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr8:131429000-131454800	Weak transcription	Aorta	Aorta
4	chr8:131429200-131444800	Weak transcription	HSMMtube	muscle
5	chr8:131429400-131440200	Weak transcription	Pancreas	Pancrea
6	chr8:131429400-131442600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr8:131429400-131447200	Weak transcription	Gastric	stomach
8	chr8:131429400-131449400	Weak transcription	Brain Hippocampus Middle	brain
9	chr8:131429600-131453800	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr8:131431600-131442600	Weak transcription	Muscle Satellite Cultured Cells	--
11	chr8:131432000-131445000	Weak transcription	Psoas Muscle	Psoas
12	chr8:131432200-131439800	Weak transcription	NHDF-Ad	bronchial
13	chr8:131432200-131449400	Weak transcription	Ovary	ovary
14	chr8:131432400-131441600	Weak transcription	Fetal Muscle Trunk	muscle
15	chr8:131432400-131441600	Weak transcription	Osteobl	bone
16	chr8:131432400-131442000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr8:131433800-131440800	Weak transcription	Right Ventricle	heart
18	chr8:131434000-131443000	Weak transcription	Skeletal Muscle Female	skeletal muscle
19	chr8:131434200-131443000	Weak transcription	Brain Substantia Nigra	brain
20	chr8:131434600-131441600	Weak transcription	Hela-S3	cervix
21	chr8:131434600-131447000	Weak transcription	HSMM	muscle
22	chr8:131434600-131447200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr8:131434800-131442000	Weak transcription	Fetal Stomach	stomach
24	chr8:131434800-131442200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr8:131434800-131453000	Weak transcription	Placenta Amnion	Placenta Amnion
26	chr8:131435000-131441400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr8:131435000-131446600	Weak transcription	NH-A	brain
28	chr8:131435200-131440800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr8:131435200-131441400	Weak transcription	Fetal Muscle Leg	muscle
30	chr8:131435200-131442000	Weak transcription	HUVEC	blood vessel
31	chr8:131435200-131442200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr8:131435200-131442200	Weak transcription	Left Ventricle	heart
33	chr8:131435200-131443400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr8:131435800-131439800	Weak transcription	HMEC	breast
35	chr8:131435800-131441000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr8:131435800-131441600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
37	chr8:131435800-131443200	Weak transcription	Stomach Smooth Muscle	stomach
38	chr8:131437000-131440000	Weak transcription	Lung	lung
39	chr8:131437000-131440600	Weak transcription	H9 Cell Line	embryonic stem cell
40	chr8:131437000-131441200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
41	chr8:131437000-131442600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr8:131437000-131449800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
43	chr8:131437000-131449800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
44	chr8:131437800-131439400	Strong transcription	Cortex derived primary cultured neurospheres	brain
45	chr8:131437800-131443400	Weak transcription	Primary B cells from peripheral blood	blood
46	chr8:131438000-131440800	Genic enhancers	A549	lung
47	chr8:131438000-131441800	Strong transcription	NHEK	skin
48	chr8:131438200-131439400	Enhancers	H1 Cell Line	embryonic stem cell
49	chr8:131438200-131440400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr8:131438200-131443600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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