Variant report

Variant	esv2761441
Chromosome Location	chr8:86155592-86167129
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:525)
CpG islands
(count:916)
Chromatin interactive
region (count:12)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:525 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:86157652-86158712	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:86158415-86158709	K562	blood:	n/a	n/a
3	ATF2	chr8:86157875-86158542	GM12878	blood:	n/a	n/a
4	BACH1	chr8:86157639-86158022	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL11A	chr8:86157928-86158378	GM12878	blood:	n/a	chr8:86158031-86158040 chr8:86157939-86157952
6	BCL11A	chr8:86157976-86158313	GM12878	blood:	n/a	chr8:86158031-86158040
7	BCLAF1	chr8:86157667-86158520	GM12878	blood:	n/a	chr8:86158031-86158040 chr8:86157939-86157952 chr8:86157687-86157696 chr8:86157680-86157689
8	BCLAF1	chr8:86157884-86158467	GM12878	blood:	n/a	chr8:86158031-86158040 chr8:86157939-86157952
9	BHLHE40	chr8:86157520-86158686	K562	blood:	n/a	chr8:86157942-86157958 chr8:86157939-86157955
10	BHLHE40	chr8:86157667-86158398	GM12878	blood:	n/a	chr8:86157942-86157958 chr8:86157939-86157955
11	BRCA1	chr8:86158193-86158399	HepG2	liver:	n/a	n/a
12	BRCA1	chr8:86157888-86157939	HepG2	liver:	n/a	n/a
13	CBX3	chr8:86157310-86158429	K562	blood:	n/a	n/a
14	CCNT2	chr8:86157563-86158468	K562	blood:	n/a	n/a
15	CEBPB	chr8:86157475-86158641	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr8:86158054-86158745	HepG2	liver:	n/a	n/a
17	CEBPB	chr8:86158023-86158727	K562	blood:	n/a	n/a
18	CEBPB	chr8:86158272-86158702	A549	lung:	n/a	n/a
19	CEBPB	chr8:86158135-86158659	IMR90	lung:	n/a	n/a
20	CHD2	chr8:86157526-86158515	GM12878	blood:	n/a	chr8:86158099-86158106
21	CHD2	chr8:86157449-86158363	HepG2	liver:	n/a	chr8:86158099-86158106
22	CHD2	chr8:86157787-86158228	H1-hESC	embryonic stem cell:	n/a	chr8:86158099-86158106
23	CHD2	chr8:86157596-86158222	K562	blood:	n/a	chr8:86158099-86158106
24	CHD2	chr8:86157632-86158032	Hela-S3	cervix:	n/a	n/a
25	CREB1	chr8:86157907-86158596	H1-hESC	embryonic stem cell:	n/a	n/a
26	CREB1	chr8:86157756-86158552	GM12878	blood:	n/a	n/a
27	CREB1	chr8:86157671-86158660	HepG2	liver:	n/a	n/a
28	CTBP2	chr8:86157295-86158374	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr8:86157742-86158133	K562	blood:	n/a	n/a
30	CTCF	chr8:86157812-86157986	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr8:86157819-86157992	MCF-7	breast:	n/a	n/a
32	CTCF	chr8:86157840-86157990	HCT-116	colon:	n/a	n/a
33	CTCF	chr8:86157811-86157926	GM13977	blood:	n/a	n/a
34	CTCF	chr8:86157811-86157998	GM12878	blood:	n/a	n/a
35	CTCF	chr8:86157800-86157950	AoAF	blood vessel:	n/a	n/a
36	CTCF	chr8:86157260-86157410	HFF-Myc	foreskin:	n/a	n/a
37	CTCF	chr8:86157860-86158010	GM12870	blood:	n/a	n/a
38	CTCF	chr8:86157800-86157950	A549	lung:	n/a	n/a
39	CTCF	chr8:86157801-86157996	ProgFib	skin:	n/a	n/a
40	CTCF	chr8:86157780-86157930	GM12868	blood:	n/a	n/a
41	CTCF	chr8:86157800-86157950	HVMF	connective:	n/a	n/a
42	CTCF	chr8:86158400-86158550	HCM	heart:	n/a	n/a
43	CTCF	chr8:86157800-86157950	GM12867	blood:	n/a	n/a
44	CTCF	chr8:86157781-86158018	MCF-7	breast:	n/a	n/a
45	CTCF	chr8:86157740-86157890	WI-38	lung:	n/a	n/a
46	CTCF	chr8:86157743-86158098	K562	blood:	n/a	n/a
47	CTCF	chr8:86157760-86157910	RPTEC	kidney:	n/a	n/a
48	CTCF	chr8:86157760-86157910	HMF	breast:	n/a	n/a
49	CTCF	chr8:86157880-86158030	NB4	blood:	n/a	n/a
50	CTCF	chr8:86157760-86157910	NHEK	skin:	n/a	n/a

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:86157393-86157443	LNCaP	prostate:	n/a
2	chr8:86157393-86157443	LNCaP	prostate:	n/a
3	chr8:86160306-86160356	GM06990	blood:	n/a
4	chr8:86158305-86158355	HepG2	liver:	n/a
5	chr8:86157501-86157551	AG10803	skin:	n/a
6	chr8:86157935-86157985	SK-N-SH_RA	brain:	n/a
7	chr8:86157410-86157460	HCF	heart:	n/a
8	chr8:86157735-86157785	CMK	blood:	n/a
9	chr8:86160306-86160356	HCM	heart:	n/a
10	chr8:86157501-86157551	HMEC	breast:	n/a
11	chr8:86157573-86157623	Jurkat	blood:	n/a
12	chr8:86157838-86157888	HRCEpiC	kidney:	n/a
13	chr8:86157735-86157785	GM06990	blood:	n/a
14	chr8:86157410-86157460	HRE	kidney:	n/a
15	chr8:86157501-86157551	AG04449	skin:	fetal
16	chr8:86157735-86157785	NT2-D1	testis:	n/a
17	chr8:86158305-86158355	AG09309	skin:	n/a
18	chr8:86157573-86157623	HL-60	blood:	n/a
19	chr8:86157410-86157460	SK-N-SH_RA	brain:	n/a
20	chr8:86158305-86158355	MCF-7	breast:	n/a
21	chr8:86157735-86157785	K562	blood:	n/a
22	chr8:86158305-86158355	PFSK-1	brain:	n/a
23	chr8:86157610-86157660	HEEpiC	esophagus:	n/a
24	chr8:86158163-86158213	GM12892	blood:	n/a
25	chr8:86157573-86157623	RPTEC	kidney:	n/a
26	chr8:86157573-86157623	PrEC	prostate:	n/a
27	chr8:86157836-86157886	ovcar-3	ovarian:	n/a
28	chr8:86157573-86157623	AG09319	gingival:	n/a
29	chr8:86157836-86157886	AoSMC	blood vessel:	n/a
30	chr8:86157525-86157575	SAEC	small airway:	n/a
31	chr8:86157838-86157888	Hepatocyte	liver:	n/a
32	chr8:86157393-86157443	PFSK-1	brain:	n/a
33	chr8:86157935-86157985	Caco-2	colon:	n/a
34	chr8:86157501-86157551	NH-A	brain:	n/a
35	chr8:86157935-86157985	MCF-7	breast:	n/a
36	chr8:86157410-86157460	PANC-1	pancreas:	n/a
37	chr8:86157735-86157785	PrEC	prostate:	n/a
38	chr8:86157641-86157691	SK-N-SH_RA	brain:	n/a
39	chr8:86157836-86157886	GM19239	blood:	n/a
40	chr8:86157735-86157785	HRE	kidney:	n/a
41	chr8:86157610-86157660	AG09319	gingival:	n/a
42	chr8:86157610-86157660	MCF10A-Er-Src	breast:	n/a
43	chr8:86157573-86157623	BJ	skin:	n/a
44	chr8:86157838-86157888	AG09309	skin:	n/a
45	chr8:86157836-86157886	AG10803	skin:	n/a
46	chr8:86157501-86157551	NB4	blood:	n/a
47	chr8:86157641-86157691	SKMC	muscle:	n/a
48	chr8:86157410-86157460	HRPEpiC	eye:	n/a
49	chr8:86160306-86160356	NH-A	brain:	n/a
50	chr8:86157501-86157551	NT2-D1	testis:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:86130126..86132730-chr8:86156867..86158422,2	K562	blood:
2	chr8:86156869..86159520-chr8:86162595..86165209,2	K562	blood:
3	chr8:86131617..86133252-chr8:86160556..86162129,2	MCF-7	breast:
4	chr8:86156067..86157846-chr8:86165485..86167515,2	K562	blood:
5	chr8:86156144..86157901-chr8:86162540..86165209,2	K562	blood:
6	chr8:86132529..86133453-chr8:86157485..86158364,3	K562	blood:
7	chr8:86132667..86134494-chr8:86156330..86158323,2	K562	blood:
8	chr8:86156346..86159536-chr8:86165485..86168710,4	K562	blood:
9	chr8:86132561..86133614-chr8:86157413..86158314,7	MCF-7	breast:
10	chr8:86088395..86090323-chr8:86154916..86157479,2	K562	blood:
11	chr8:86166893..86168765-chr8:86170470..86172602,2	K562	blood:
12	chr8:86158140..86160236-chr8:86162041..86163568,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-219B4.5.1-1	chr8:86157624-86157946	NONHSAT127522
2	lnc-RP11-219B4.5.1-1	chr8:86155574-86155917	NONHSAT127522

No data

Variant related genes	Relation type
ENSG00000258256	TF binding region
ENSG00000257962	TF binding region
CA13	TF binding region
ENSG00000258256	CpG island
ENSG00000257962	CpG island
CA13	CpG island
ENSG00000185015	chromatin interactions
ENSG00000133740	chromatin interactions
ENSG00000257962	chromatin interactions
ENSG00000260493	chromatin interactions
ENSG00000176731	chromatin interactions
ENSG00000258256	chromatin interactions

Extended variants
information (count: 449 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:449 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568790523	chr8:86155597-86155598	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
2	rs533370992	chr8:86155599-86155600	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
3	rs376693184	chr8:86155689-86155690	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
4	rs563646947	chr8:86155693-86155694	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
5	rs187645917	chr8:86155700-86155701	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
6	rs191957693	chr8:86155782-86155783	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
7	rs183782216	chr8:86155807-86155808	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
8	rs371381160	chr8:86155867-86155868	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
9	rs534468664	chr8:86155872-86155873	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
10	rs186692453	chr8:86155892-86155893	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
11	rs28523659	chr8:86155908-86155909	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs533717908	chr8:86155926-86155927	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs13259464	chr8:86155928-86155929	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs536660454	chr8:86155930-86155931	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs556948486	chr8:86155933-86155934	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs573533510	chr8:86156051-86156052	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs536390224	chr8:86156053-86156054	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs191476141	chr8:86156121-86156122	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs373762604	chr8:86156131-86156132	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs373731354	chr8:86156168-86156169	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs147688035	chr8:86156171-86156172	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs541594092	chr8:86156175-86156176	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs73688688	chr8:86156176-86156177	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs578241456	chr8:86156236-86156237	Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs182429386	chr8:86156282-86156283	Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs186663652	chr8:86156283-86156284	Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs572664688	chr8:86156366-86156367	Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs529269386	chr8:86156369-86156370	Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs547251828	chr8:86156400-86156401	Weak transcription Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs543116185	chr8:86156415-86156416	Weak transcription Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs559372439	chr8:86156475-86156476	Weak transcription Bivalent Enhancer ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs191123409	chr8:86156520-86156521	Weak transcription Bivalent Enhancer ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs535124421	chr8:86156548-86156549	Weak transcription Bivalent Enhancer ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs571090636	chr8:86156587-86156588	Weak transcription Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs530860587	chr8:86156596-86156597	Weak transcription Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs149177726	chr8:86156599-86156600	Weak transcription Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs182161719	chr8:86156607-86156608	Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs574813812	chr8:86156652-86156653	Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs4740044	chr8:86156680-86156681	Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs553109927	chr8:86156691-86156692	Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs143233533	chr8:86156696-86156697	Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs4740045	chr8:86156707-86156708	Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs148301940	chr8:86156783-86156784	Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs578094768	chr8:86156801-86156802	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs544143076	chr8:86156824-86156825	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs576027792	chr8:86156858-86156859	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs573980264	chr8:86157027-86157028	Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs189235501	chr8:86157055-86157056	Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs559435226	chr8:86157065-86157066	Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs193054332	chr8:86157109-86157110	Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
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
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	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	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	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
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
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
small cell lung cancer	20016488	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
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Epilepsy	20502679	CNVD
Acute monocytic leukemia	16498392	CNVD
Autism	20841430	CNVD
Gastric cancer	22014070	CNVD

Chromatin state (count:438 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:86133800-86157200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr8:86134600-86157200	Weak transcription	Right Atrium	heart
3	chr8:86136000-86157200	Weak transcription	Liver	Liver
4	chr8:86136200-86157000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr8:86136400-86157000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr8:86139600-86157200	Weak transcription	Pancreas	Pancrea
7	chr8:86142600-86157200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr8:86143600-86157000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr8:86145000-86157200	Weak transcription	Ovary	ovary
10	chr8:86145600-86157400	Weak transcription	Brain Angular Gyrus	brain
11	chr8:86146200-86156400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr8:86146200-86157200	Weak transcription	Gastric	stomach
13	chr8:86148000-86157200	Weak transcription	Esophagus	oesophagus
14	chr8:86148200-86157200	Weak transcription	Brain Inferior Temporal Lobe	brain
15	chr8:86149200-86157000	Weak transcription	Primary monocytes fromperipheralblood	blood
16	chr8:86152000-86157200	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr8:86152400-86157200	Weak transcription	Rectal Mucosa Donor 31	rectum
18	chr8:86152600-86157000	Weak transcription	Stomach Mucosa	stomach
19	chr8:86152800-86157200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr8:86153000-86157000	Weak transcription	Duodenum Mucosa	Duodenum
21	chr8:86153200-86157000	Weak transcription	Fetal Intestine Large	intestine
22	chr8:86153200-86157200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
23	chr8:86154000-86157000	Weak transcription	Fetal Intestine Small	intestine
24	chr8:86154600-86157200	Weak transcription	HepG2	liver
25	chr8:86155000-86156800	Weak transcription	Monocytes-CD14+_RO01746	blood
26	chr8:86155400-86155600	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr8:86155400-86155600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr8:86156000-86157200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr8:86156200-86156800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
30	chr8:86156400-86156600	ZNF genes & repeats	Thymus	Thymus
31	chr8:86156600-86157200	Weak transcription	Thymus	Thymus
32	chr8:86156800-86157000	Enhancers	Monocytes-CD14+_RO01746	blood
33	chr8:86156800-86157200	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
34	chr8:86156800-86157200	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
35	chr8:86157000-86157200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr8:86157000-86157200	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
37	chr8:86157000-86157200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr8:86157000-86157200	Enhancers	Primary monocytes fromperipheralblood	blood
39	chr8:86157000-86157200	Bivalent/Poised TSS	Primary B cells from cord blood	blood
40	chr8:86157000-86157200	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells	blood
41	chr8:86157000-86157200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
42	chr8:86157000-86157200	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
43	chr8:86157000-86157200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
44	chr8:86157000-86157200	Active TSS	Primary T killer memory cells from peripheral blood	blood
45	chr8:86157000-86157200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr8:86157000-86157200	Enhancers	Cortex derived primary cultured neurospheres	brain
47	chr8:86157000-86157200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr8:86157000-86157200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr8:86157000-86157200	Enhancers	Adipose Nuclei	Adipose
50	chr8:86157000-86157200	Enhancers	Brain Anterior Caudate	brain

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