Variant report

Variant	nsv890922
Chromosome Location	chr8:54994759-55023494
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:675)
CpG islands
(count:976)
Chromatin interactive
region (count:43)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:675 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:55018717-55019091	K562	blood:	n/a	n/a
2	ARID3A	chr8:55012881-55013984	K562	blood:	n/a	n/a
3	ARID3A	chr8:55012852-55014180	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:55006625-55006885	K562	blood:	n/a	n/a
5	ARID3A	chr8:55014439-55014825	HepG2	liver:	n/a	n/a
6	ARID3A	chr8:55014700-55014793	K562	blood:	n/a	n/a
7	ATF1	chr8:55018643-55019258	K562	blood:	n/a	n/a
8	ATF2	chr8:55014498-55014923	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr8:55014571-55014784	K562	blood:	n/a	n/a
10	BACH1	chr8:55013899-55014674	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCLAF1	chr8:55014129-55014597	GM12878	blood:	n/a	chr8:55014572-55014581
12	BHLHE40	chr8:55012805-55012905	K562	blood:	n/a	n/a
13	BHLHE40	chr8:55013765-55013986	GM12878	blood:	n/a	n/a
14	BHLHE40	chr8:55018810-55019419	K562	blood:	n/a	n/a
15	BHLHE40	chr8:55014303-55014813	HepG2	liver:	n/a	chr8:55014627-55014643 chr8:55014526-55014542
16	BHLHE40	chr8:55013215-55015126	K562	blood:	n/a	chr8:55014627-55014643 chr8:55014526-55014542
17	BHLHE40	chr8:55014229-55014895	GM12878	blood:	n/a	chr8:55014627-55014643 chr8:55014526-55014542
18	BRCA1	chr8:55014673-55014700	HepG2	liver:	n/a	n/a
19	BRCA1	chr8:55014723-55014734	GM12878	blood:	n/a	n/a
20	CBX3	chr8:55014325-55015500	K562	blood:	n/a	n/a
21	CBX3	chr8:54999398-54999689	K562	blood:	n/a	n/a
22	CBX3	chr8:54999180-54999711	K562	blood:	n/a	n/a
23	CBX3	chr8:55002517-55002905	K562	blood:	n/a	n/a
24	CCNT2	chr8:55013643-55014772	K562	blood:	n/a	n/a
25	CCNT2	chr8:55012910-55013110	K562	blood:	n/a	n/a
26	CEBPB	chr8:55008562-55008673	A549	lung:	n/a	n/a
27	CEBPB	chr8:55002053-55002401	A549	lung:	n/a	n/a
28	CEBPB	chr8:55014474-55014861	K562	blood:	n/a	chr8:55014622-55014630
29	CEBPB	chr8:55014326-55014842	A549	lung:	n/a	chr8:55014622-55014630
30	CEBPB	chr8:55002072-55002366	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr8:55014377-55014967	A549	lung:	n/a	chr8:55014622-55014630
32	CEBPB	chr8:55014507-55014754	HepG2	liver:	n/a	chr8:55014622-55014630
33	CEBPB	chr8:55013339-55013805	K562	blood:	n/a	n/a
34	CEBPB	chr8:55013410-55013849	K562	blood:	n/a	n/a
35	CEBPB	chr8:55014550-55014855	A549	lung:	n/a	chr8:55014622-55014630
36	CEBPB	chr8:55010706-55011064	IMR90	lung:	n/a	n/a
37	CEBPB	chr8:55014470-55014865	K562	blood:	n/a	chr8:55014622-55014630
38	CEBPB	chr8:55010713-55011013	K562	blood:	n/a	n/a
39	CEBPB	chr8:55002036-55002415	K562	blood:	n/a	n/a
40	CEBPB	chr8:55013452-55013759	A549	lung:	n/a	n/a
41	CEBPB	chr8:55011752-55011825	K562	blood:	n/a	n/a
42	CEBPB	chr8:55011746-55011946	HepG2	liver:	n/a	chr8:55011916-55011927
43	CEBPB	chr8:55013423-55013799	HepG2	liver:	n/a	n/a
44	CEBPB	chr8:55013426-55013795	IMR90	lung:	n/a	n/a
45	CEBPB	chr8:55014564-55014742	K562	blood:	n/a	chr8:55014622-55014630
46	CEBPB	chr8:55002058-55002368	K562	blood:	n/a	n/a
47	CEBPB	chr8:55002050-55002410	HepG2	liver:	n/a	n/a
48	CEBPB	chr8:55014301-55014850	HepG2	liver:	n/a	chr8:55014622-55014630
49	CEBPB	chr8:55013118-55014920	Hela-S3	cervix:	n/a	chr8:55014622-55014630
50	CEBPB	chr8:55014497-55014838	H1-hESC	embryonic stem cell:	n/a	chr8:55014622-55014630

(count:976 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:55014888-55014938	HEK293	kidney:	embryo
2	chr8:55014641-55014691	GM12891	blood:	n/a
3	chr8:55014643-55014693	HCF	heart:	n/a
4	chr8:55014655-55014705	NH-A	brain:	n/a
5	chr8:55014655-55014705	H1-hESC	embryonic stem cell:	embryo
6	chr8:55016879-55016929	NHDF-neo	bronchial:	n/a
7	chr8:55011819-55011869	NT2-D1	testis:	n/a
8	chr8:55014655-55014705	HNPCEpiC	eye:	n/a
9	chr8:55011819-55011869	CMK	blood:	n/a
10	chr8:55014377-55014427	Hepatocyte	liver:	n/a
11	chr8:55014847-55014897	LNCaP	prostate:	n/a
12	chr8:54997999-54998049	NHDF-neo	bronchial:	n/a
13	chr8:54997999-54998049	HUVEC	blood vessel:	n/a
14	chr8:55016751-55016801	IMR90	lung:	fetal
15	chr8:55014655-55014705	AG10803	skin:	n/a
16	chr8:55014772-55014822	U87	brain:	n/a
17	chr8:55014772-55014822	GM12891	blood:	n/a
18	chr8:55014040-55014090	H1-hESC	embryonic stem cell:	embryo
19	chr8:55014772-55014822	LNCaP	prostate:	n/a
20	chr8:55014772-55014822	HEK293	kidney:	embryo
21	chr8:55011819-55011869	IMR90	lung:	fetal
22	chr8:55012178-55012228	Caco-2	colon:	n/a
23	chr8:55016751-55016801	NT2-D1	testis:	n/a
24	chr8:55014772-55014822	GM06990	blood:	n/a
25	chr8:55016879-55016929	LNCaP	prostate:	n/a
26	chr8:55014847-55014897	AG09309	skin:	n/a
27	chr8:55014772-55014822	MCF10A-Er-Src	breast:	n/a
28	chr8:55012178-55012228	GM12892	blood:	n/a
29	chr8:55014888-55014938	MCF10A-Er-Src	breast:	n/a
30	chr8:55014888-55014938	PANC-1	pancreas:	n/a
31	chr8:55011819-55011869	U87	brain:	n/a
32	chr8:55011819-55011869	AG09309	skin:	n/a
33	chr8:55014772-55014822	CMK	blood:	n/a
34	chr8:55014388-55014438	SK-N-SH_RA	brain:	n/a
35	chr8:55016930-55016980	SAEC	small airway:	n/a
36	chr8:55012178-55012228	HPAEpiC	pulmonary alveolar:	n/a
37	chr8:55011819-55011869	PFSK-1	brain:	n/a
38	chr8:55011819-55011869	K562	blood:	n/a
39	chr8:55014772-55014822	ECC-1	luminal epithelium:	n/a
40	chr8:55016879-55016929	Jurkat	blood:	n/a
41	chr8:55014847-55014897	PrEC	prostate:	n/a
42	chr8:55011819-55011869	HPAEpiC	pulmonary alveolar:	n/a
43	chr8:55014388-55014438	NHDF-neo	bronchial:	n/a
44	chr8:55014388-55014438	HRE	kidney:	n/a
45	chr8:55014641-55014691	HAEpiC	amniotic membrane:	n/a
46	chr8:55014847-55014897	NT2-D1	testis:	n/a
47	chr8:55014388-55014438	BJ	skin:	n/a
48	chr8:55014888-55014938	HUVEC	blood vessel:	n/a
49	chr8:55014377-55014427	LNCaP	prostate:	n/a
50	chr8:55014772-55014822	GM12892	blood:	n/a

(count:43 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:55011828..55016126-chr8:55017682..55020090,4	K562	blood:
2	chr8:55012759..55014929-chr8:55046340..55050101,4	K562	blood:
3	chr8:55005117..55006971-chr8:55012903..55014492,2	K562	blood:
4	chr8:55011828..55014733-chr8:55017986..55020090,2	K562	blood:
5	chr8:54996725..55000204-chr8:55012427..55016239,5	K562	blood:
6	chr8:9412503..9413441-chr8:55013581..55014482,2	Hela-S3	cervix:
7	chr8:54791520..54793289-chr8:55017925..55020342,2	K562	blood:
8	chr5:162886981..162887825-chr8:55014104..55014735,2	NB4	blood:
9	chr20:45946400..45948172-chr8:55014333..55016301,2	MCF-7	breast:
10	chr8:55022281..55024042-chr8:55030500..55032091,2	K562	blood:
11	chr8:55003709..55008030-chr8:55008912..55012851,6	K562	blood:
12	chr8:54933970..54936104-chr8:55012695..55015394,2	MCF-7	breast:
13	chr8:55007468..55010231-chr8:55019347..55021686,2	K562	blood:
14	chr8:54931365..54936825-chr8:55013053..55016452,9	MCF-7	breast:
15	chr8:55003709..55008030-chr8:55008912..55012851,6	K562	blood:
16	chr8:55012036..55017270-chr8:55017780..55022488,6	MCF-7	breast:
17	chr8:55012232..55015363-chr8:55063151..55067460,5	K562	blood:
18	chr8:54996188..54999075-chr8:55012427..55015650,3	K562	blood:
19	chr8:55013205..55015046-chr8:55046385..55049225,2	MCF-7	breast:
20	chr8:55008979..55011480-chr8:55012604..55016082,4	K562	blood:
21	chr8:54990352..54992315-chr8:55004670..55007174,2	K562	blood:
22	chr8:55021464..55024057-chr8:55046548..55048568,2	MCF-7	breast:
23	chr1:43147767..43148594-chr8:55013821..55014667,2	HCT-116	colon:
24	chr8:55017880..55020655-chr8:55046123..55048427,3	MCF-7	breast:
25	chr8:55005836..55007387-chr8:55012760..55014510,2	MCF-7	breast:
26	chr8:54929833..54936668-chr8:55008421..55016367,12	K562	blood:
27	chr8:55007468..55010231-chr8:55019347..55021686,2	K562	blood:
28	chr8:54934501..54937318-chr8:55011753..55013857,2	K562	blood:
29	chr8:54934843..54936668-chr8:55008922..55011513,2	K562	blood:
30	chr8:55012350..55016130-chr8:55063151..55067016,6	K562	blood:
31	chr8:55006677..55009466-chr8:55047209..55049239,2	MCF-7	breast:
32	chr8:54791937..54794536-chr8:55012642..55014305,2	K562	blood:
33	chr8:55008237..55011334-chr8:55014384..55018005,3	MCF-7	breast:
34	chr8:55013237..55015721-chr8:55016855..55019742,2	MCF-7	breast:
35	chr8:55011657..55013589-chr8:55059186..55062088,2	K562	blood:
36	chr8:54990580..54994755-chr8:55009285..55012320,3	K562	blood:
37	chr8:55009975..55010673-chr8:55078381..55079050,2	MCF-7	breast:
38	chr8:55014583..55016959-chr8:55047205..55048947,2	K562	blood:
39	chr8:55012569..55016203-chr8:55046168..55049938,7	MCF-7	breast:
40	chr8:55003346..55005748-chr8:55012113..55014512,3	MCF-7	breast:
41	chr8:54924177..54926194-chr8:55016876..55019206,2	K562	blood:
42	chr8:54990580..54993539-chr8:55009667..55012320,2	K562	blood:
43	chr8:55010890..55013599-chr8:55056433..55059069,2	MCF-7	breast:

No data

Variant related genes	Relation type
LYPLA1	TF binding region
LYPLA1	CpG island
ENSG00000267882	chromatin interactions
ENSG00000120992	chromatin interactions
ENSG00000147509	chromatin interactions
ENSG00000173273	chromatin interactions
ENSG00000137547	chromatin interactions
ENSG00000187735	chromatin interactions
ENSG00000170584	chromatin interactions
ENSG00000251835	chromatin interactions
ENSG00000065978	chromatin interactions
ENSG00000072571	chromatin interactions
ENSG00000101040	chromatin interactions

Extended variants
information (count: 1113 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:1113 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs34599244	chr8:54994759-54994760	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs73681307	chr8:54994785-54994786	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs193250877	chr8:54994798-54994799	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs537810950	chr8:54994806-54994807	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs547883733	chr8:54994818-54994819	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs568319174	chr8:54994825-54994826	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs533852963	chr8:54994835-54994836	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs184849544	chr8:54994841-54994842	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs372180572	chr8:54994842-54994843	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs188882874	chr8:54994856-54994857	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs79465602	chr8:54994868-54994869	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs181637246	chr8:54994892-54994893	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs576468442	chr8:54994897-54994898	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs538960939	chr8:54994948-54994949	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs185362340	chr8:54994949-54994950	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs572740599	chr8:54994972-54994973	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs528510896	chr8:54994974-54994975	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs375820111	chr8:54995010-54995011	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs138171709	chr8:54995025-54995026	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs11998000	chr8:54995058-54995059	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs112313904	chr8:54995060-54995061	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs533612106	chr8:54995110-54995111	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs544042233	chr8:54995123-54995124	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs189918654	chr8:54995127-54995128	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs562558047	chr8:54995182-54995183	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs180726821	chr8:54995193-54995194	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs373535757	chr8:54995196-54995197	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs35130790	chr8:54995198-54995199	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs567998566	chr8:54995219-54995220	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs527560819	chr8:54995256-54995257	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs376937395	chr8:54995267-54995268	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs547336071	chr8:54995309-54995310	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs570305401	chr8:54995310-54995311	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs539206039	chr8:54995350-54995351	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs556086538	chr8:54995382-54995383	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs570106047	chr8:54995399-54995400	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs545365092	chr8:54995411-54995412	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs564271592	chr8:54995444-54995445	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs535592216	chr8:54995460-54995461	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs141805380	chr8:54995508-54995509	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs572498226	chr8:54995515-54995516	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs186061807	chr8:54995528-54995529	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs558527862	chr8:54995532-54995533	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs553433355	chr8:54995533-54995534	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs578251411	chr8:54995537-54995538	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs549768430	chr8:54995541-54995542	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs145143807	chr8:54995574-54995575	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs569520470	chr8:54995575-54995576	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs138966333	chr8:54995581-54995582	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs541589380	chr8:54995588-54995589	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
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
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Salivary gland tumor	18059337	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
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	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
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
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	22286061	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Sezary syndrome	18413736	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Uveal melanoma	20484589	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:1223 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:54946400-54999200	Weak transcription	NHDF-Ad	bronchial
2	chr8:54949800-54999400	Weak transcription	NHLF	lung
3	chr8:54956000-54999000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
4	chr8:54957600-55009800	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr8:54963200-54999200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
6	chr8:54963200-54999200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr8:54963200-54999200	Weak transcription	Colonic Mucosa	Colon
8	chr8:54963200-54999200	Weak transcription	Small Intestine	intestine
9	chr8:54963400-54999200	Weak transcription	HSMMtube	muscle
10	chr8:54963800-54999200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
11	chr8:54966200-54997600	Weak transcription	Pancreas	Pancrea
12	chr8:54966400-55007600	Weak transcription	Psoas Muscle	Psoas
13	chr8:54966400-55012800	Weak transcription	Fetal Kidney	kidney
14	chr8:54966600-55012800	Weak transcription	Rectal Smooth Muscle	rectum
15	chr8:54967200-54999200	Weak transcription	Ovary	ovary
16	chr8:54974400-54999200	Weak transcription	Rectal Mucosa Donor 31	rectum
17	chr8:54974600-54997400	Weak transcription	Spleen	Spleen
18	chr8:54974600-54999200	Weak transcription	Right Ventricle	heart
19	chr8:54974800-54999200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
20	chr8:54974800-55002200	Weak transcription	Gastric	stomach
21	chr8:54975600-55012800	Weak transcription	Stomach Smooth Muscle	stomach
22	chr8:54975800-54999200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
23	chr8:54975800-54999600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
24	chr8:54982600-54999400	Weak transcription	HSMM	muscle
25	chr8:54983800-54999200	Weak transcription	Skeletal Muscle Male	skeletal muscle
26	chr8:54984000-55005800	Weak transcription	Skeletal Muscle Female	skeletal muscle
27	chr8:54985000-54999200	Weak transcription	Fetal Brain Female	brain
28	chr8:54986000-54997600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr8:54986000-54999200	Weak transcription	Cortex derived primary cultured neurospheres	brain
30	chr8:54986200-55000000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr8:54987400-54994800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr8:54988000-54999000	Weak transcription	Placenta Amnion	Placenta Amnion
33	chr8:54989200-54999200	Weak transcription	Colon Smooth Muscle	Colon
34	chr8:54989400-54995200	Strong transcription	Monocytes-CD14+_RO01746	blood
35	chr8:54989400-54996400	Strong transcription	A549	lung
36	chr8:54989600-54995000	Strong transcription	Primary monocytes fromperipheralblood	blood
37	chr8:54989600-54995200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
38	chr8:54989600-54999000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr8:54990000-54995400	Strong transcription	HUES64 Cell Line	embryonic stem cell
40	chr8:54990000-54999000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
41	chr8:54990400-54999200	Weak transcription	HMEC	breast
42	chr8:54990800-54994800	Strong transcription	Fetal Thymus	thymus
43	chr8:54990800-54996400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
44	chr8:54991000-54994800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
45	chr8:54991000-54995000	Strong transcription	HepG2	liver
46	chr8:54991000-54996200	Strong transcription	K562	blood
47	chr8:54991200-54994800	Strong transcription	Primary neutrophils fromperipheralblood	blood
48	chr8:54991200-54994800	Strong transcription	Primary T helper cells PMA-I stimulated	--
49	chr8:54991200-54994800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
50	chr8:54991200-54995000	Strong transcription	Dnd41	blood

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