Variant report

Variant	esv3448910
Chromosome Location	chr8:11144417-11146865
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:26)
CpG islands
(count:61)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:26 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ELF1	chr8:11145939-11146343	K562	blood:	n/a	chr8:11146153-11146166
2	EP300	chr8:11144264-11144706	T-47D	breast:	n/a	n/a
3	FOS	chr8:11146863-11147215	MCF10A-Er-Src	breast:	n/a	n/a
4	FOXA1	chr8:11144637-11144942	T-47D	breast:	n/a	n/a
5	FOXA1	chr8:11144257-11144617	T-47D	breast:	n/a	n/a
6	FOXA1	chr8:11144196-11144977	T-47D	breast:	n/a	n/a
7	GATA3	chr8:11144258-11144704	T-47D	breast:	n/a	n/a
8	GATA3	chr8:11144280-11144711	T-47D	breast:	n/a	n/a
9	JUND	chr8:11144203-11144798	T-47D	breast:	n/a	n/a
10	JUND	chr8:11146858-11147253	HepG2	liver:	n/a	chr8:11147042-11147053
11	JUND	chr8:11146821-11147253	Hela-S3	cervix:	n/a	chr8:11147042-11147053
12	JUND	chr8:11146743-11147444	SK-N-SH	brain:	n/a	chr8:11147042-11147053
13	KAP1	chr8:11146713-11147684	U2OS	brain:	n/a	n/a
14	KAP1	chr8:11146674-11147683	HEK293	kidney:	n/a	n/a
15	MAFF	chr8:11146864-11147281	HepG2	liver:	n/a	chr8:11147042-11147060
16	MAFK	chr8:11146863-11147232	HepG2	liver:	n/a	chr8:11147043-11147058
17	MAFK	chr8:11146863-11147274	IMR90	lung:	n/a	chr8:11147043-11147058
18	MAFK	chr8:11146865-11147239	K562	blood:	n/a	chr8:11147043-11147058
19	MAFK	chr8:11146797-11147348	H1-hESC	embryonic stem cell:	n/a	chr8:11147043-11147058
20	MAFK	chr8:11146861-11147235	HepG2	liver:	n/a	chr8:11147043-11147058
21	MAFK	chr8:11146861-11147224	Hela-S3	cervix:	n/a	chr8:11147043-11147058
22	NFYB	chr8:11144605-11144770	Hela-S3	cervix:	n/a	n/a
23	POLR2A	chr8:11144826-11144844	GM12878	blood:	n/a	n/a
24	POLR2A	chr8:11144315-11144477	MCF10A-Er-Src	breast:	n/a	n/a
25	WRNIP1	chr8:11145959-11146142	GM12878	blood:	n/a	n/a
26	ZNF274	chr8:11144985-11145618	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:11144705-11144755	HIPEpiC	eye:	n/a
2	chr8:11144705-11144755	HNPCEpiC	eye:	n/a
3	chr8:11144705-11144755	BJ	skin:	n/a
4	chr8:11144705-11144755	SK-N-MC	brain:	n/a
5	chr8:11144705-11144755	AG10803	skin:	n/a
6	chr8:11144705-11144755	HRE	kidney:	n/a
7	chr8:11144705-11144755	A549	lung:	n/a
8	chr8:11144705-11144755	NT2-D1	testis:	n/a
9	chr8:11144705-11144755	HRPEpiC	eye:	n/a
10	chr8:11144705-11144755	HCM	heart:	n/a
11	chr8:11144705-11144755	SK-N-SH_RA	brain:	n/a
12	chr8:11144705-11144755	NHBE	bronchial:	n/a
13	chr8:11144705-11144755	K562	blood:	n/a
14	chr8:11144705-11144755	HL-60	blood:	n/a
15	chr8:11144705-11144755	ECC-1	luminal epithelium:	n/a
16	chr8:11144705-11144755	HAEpiC	amniotic membrane:	n/a
17	chr8:11144705-11144755	H1-hESC	embryonic stem cell:	embryo
18	chr8:11144705-11144755	Caco-2	colon:	n/a
19	chr8:11144705-11144755	AG09319	gingival:	n/a
20	chr8:11144705-11144755	NB4	blood:	n/a
21	chr8:11144705-11144755	PrEC	prostate:	n/a
22	chr8:11144705-11144755	GM12891	blood:	n/a
23	chr8:11144705-11144755	U87	brain:	n/a
24	chr8:11144705-11144755	PANC-1	pancreas:	n/a
25	chr8:11144705-11144755	T-47D	breast:	n/a
26	chr8:11144705-11144755	AG04449	skin:	fetal
27	chr8:11144705-11144755	AG04450	lung:	fetal
28	chr8:11144705-11144755	SK-N-SH	brain:	n/a
29	chr8:11144705-11144755	MCF10A-Er-Src	breast:	n/a
30	chr8:11144705-11144755	HepG2	liver:	n/a
31	chr8:11144705-11144755	CMK	blood:	n/a
32	chr8:11144705-11144755	ovcar-3	ovarian:	n/a
33	chr8:11144705-11144755	ProgFib	skin:	n/a
34	chr8:11144705-11144755	HRCEpiC	kidney:	n/a
35	chr8:11144705-11144755	GM19239	blood:	n/a
36	chr8:11144705-11144755	HEK293	kidney:	embryo
37	chr8:11144705-11144755	GM12892	blood:	n/a
38	chr8:11144705-11144755	SAEC	small airway:	n/a
39	chr8:11144705-11144755	HCF	heart:	n/a
40	chr8:11144705-11144755	Hepatocyte	liver:	n/a
41	chr8:11144705-11144755	PFSK-1	brain:	n/a
42	chr8:11144705-11144755	HPAEpiC	pulmonary alveolar:	n/a
43	chr8:11144705-11144755	Jurkat	blood:	n/a
44	chr8:11144705-11144755	GM06990	blood:	n/a
45	chr8:11144705-11144755	AoSMC	blood vessel:	n/a
46	chr8:11144705-11144755	BE2_C	brain:	n/a
47	chr8:11144705-11144755	NHDF-neo	bronchial:	n/a
48	chr8:11144705-11144755	RPTEC	kidney:	n/a
49	chr8:11144705-11144755	HCT-116	colon:	n/a
50	chr8:11144705-11144755	LNCaP	prostate:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:11142561..11144389-chr8:11146083..11147788,2	MCF-7	breast:
2	chr8:11145415..11146964-chr8:11204889..11207266,2	K562	blood:
3	chr8:11146765..11148444-chr8:11152337..11154487,2	K562	blood:
4	chr8:11142870..11145744-chr8:11152405..11154351,2	K562	blood:
5	chr8:11141122..11144782-chr8:11147545..11153235,7	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000249316	TF binding region
ENSG00000249316	CpG island
ENSG00000154316	chromatin interactions
ENSG00000104643	chromatin interactions
ENSG00000255020	chromatin interactions

Extended variants
information (count: 151 )
Associated
traits (count: 138 )

Variant overlapped rSNPs/rCNVs (count:151 , 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	rs111899210	chr8:11144422-11144423	Active TSS Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs147881311	chr8:11144441-11144442	Active TSS Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs537006526	chr8:11144451-11144452	Active TSS Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs2572421	chr8:11144484-11144485	Active TSS Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs558391883	chr8:11144511-11144512	Active TSS Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs7813424	chr8:11144517-11144518	Active TSS Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs534404998	chr8:11144520-11144521	Active TSS Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs139949778	chr8:11144583-11144584	Active TSS Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs145481185	chr8:11144644-11144645	Active TSS Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs574681455	chr8:11144695-11144696	Active TSS Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs569529149	chr8:11144704-11144705	Active TSS Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs542185316	chr8:11144716-11144717	Active TSS Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs538540605	chr8:11144721-11144722	Active TSS Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs147716193	chr8:11144726-11144727	Active TSS Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs142579007	chr8:11144771-11144772	Active TSS Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs546149236	chr8:11144775-11144776	Active TSS Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs564437276	chr8:11144812-11144813	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs375101995	chr8:11144827-11144828	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs150270461	chr8:11144832-11144833	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs188477242	chr8:11144846-11144847	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs114803303	chr8:11144853-11144854	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs567792917	chr8:11144862-11144863	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs192729817	chr8:11144875-11144876	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs529408942	chr8:11144899-11144900	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs550867842	chr8:11144900-11144901	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs558339610	chr8:11144905-11144906	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs184755497	chr8:11144983-11144984	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs530440675	chr8:11145001-11145002	Weak transcription Strong transcription ZNF genes & repeats Active TSS Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs189272077	chr8:11145068-11145069	Weak transcription Strong transcription ZNF genes & repeats Active TSS Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs570330779	chr8:11145088-11145089	Weak transcription Strong transcription ZNF genes & repeats Active TSS Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs534762132	chr8:11145090-11145091	Weak transcription Strong transcription ZNF genes & repeats Active TSS Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs180953501	chr8:11145109-11145110	Weak transcription Strong transcription ZNF genes & repeats Active TSS Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs568269961	chr8:11145143-11145144	Weak transcription Strong transcription ZNF genes & repeats Active TSS Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs574897420	chr8:11145145-11145146	Weak transcription Strong transcription ZNF genes & repeats Active TSS Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs568081252	chr8:11145162-11145163	Weak transcription Strong transcription ZNF genes & repeats Active TSS Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs535598241	chr8:11145170-11145171	Weak transcription Strong transcription ZNF genes & repeats Active TSS Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs553818994	chr8:11145178-11145179	Weak transcription Strong transcription ZNF genes & repeats Active TSS Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs183582136	chr8:11145184-11145185	Weak transcription Strong transcription ZNF genes & repeats Active TSS Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs545761686	chr8:11145206-11145207	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs558157757	chr8:11145209-11145210	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs200639913	chr8:11145213-11145214	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs557198000	chr8:11145215-11145216	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs145842191	chr8:11145223-11145224	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs573149318	chr8:11145254-11145255	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs62488593	chr8:11145281-11145282	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs570720462	chr8:11145282-11145283	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs36211457	chr8:11145298-11145299	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs62488594	chr8:11145307-11145308	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs374899211	chr8:11145311-11145312	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs398047508	chr8:11145312-11145313	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:138)

Disease	PMID	Source
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
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
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
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
abnormal development	18461090	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Gastric cancer	21811585	CNVD
Colorectal cancer	16774939	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:331 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:11142800-11145000	Enhancers	Small Intestine	intestine
2	chr8:11143000-11144600	Flanking Active TSS	Dnd41	blood
3	chr8:11143000-11145000	Enhancers	Spleen	Spleen
4	chr8:11143000-11145200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
5	chr8:11143000-11145200	Enhancers	Sigmoid Colon	Sigmoid Colon
6	chr8:11143000-11146000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr8:11143000-11146000	Weak transcription	Lung	lung
8	chr8:11143000-11146200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr8:11143000-11149400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
10	chr8:11143000-11162200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr8:11143000-11166400	Weak transcription	Esophagus	oesophagus
12	chr8:11143000-11166400	Weak transcription	Pancreas	Pancrea
13	chr8:11143200-11145200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
14	chr8:11143400-11144600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr8:11143400-11144600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr8:11143400-11144600	Enhancers	Fetal Brain Male	brain
17	chr8:11143400-11144600	Weak transcription	Fetal Heart	heart
18	chr8:11143400-11144600	Active TSS	Hela-S3	cervix
19	chr8:11143400-11144800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr8:11143400-11144800	Enhancers	Liver	Liver
21	chr8:11143400-11144800	Active TSS	Rectal Smooth Muscle	rectum
22	chr8:11143400-11145000	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr8:11143400-11145000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
24	chr8:11143400-11145000	Enhancers	Primary T killer memory cells from peripheral blood	blood
25	chr8:11143400-11145000	Enhancers	Brain Germinal Matrix	brain
26	chr8:11143400-11146000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr8:11143400-11146000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr8:11143400-11146000	Weak transcription	Fetal Intestine Small	intestine
29	chr8:11143400-11146000	Weak transcription	Gastric	stomach
30	chr8:11143400-11146000	Weak transcription	NH-A	brain
31	chr8:11143400-11146200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr8:11143400-11146600	Weak transcription	HUVEC	blood vessel
33	chr8:11143400-11147000	Weak transcription	H1 Cell Line	embryonic stem cell
34	chr8:11143400-11147000	Weak transcription	H9 Cell Line	embryonic stem cell
35	chr8:11143400-11147000	Weak transcription	Brain Substantia Nigra	brain
36	chr8:11143400-11150200	Weak transcription	Osteobl	bone
37	chr8:11143400-11152800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr8:11143400-11153000	Weak transcription	NHLF	lung
39	chr8:11143400-11153200	Weak transcription	Fetal Thymus	thymus
40	chr8:11143400-11154000	Weak transcription	Psoas Muscle	Psoas
41	chr8:11143400-11163600	Weak transcription	Brain Angular Gyrus	brain
42	chr8:11143400-11166400	Weak transcription	HSMMtube	muscle
43	chr8:11143600-11144600	Weak transcription	HUES64 Cell Line	embryonic stem cell
44	chr8:11143600-11144600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr8:11143600-11146000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr8:11143800-11144600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr8:11143800-11144600	Weak transcription	Brain Inferior Temporal Lobe	brain
48	chr8:11143800-11144600	Enhancers	Duodenum Smooth Muscle	Duodenum
49	chr8:11143800-11144600	Weak transcription	Left Ventricle	heart
50	chr8:11143800-11144800	Weak transcription	Right Atrium	heart

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