Variant report

Variant	esv2761448
Chromosome Location	chr8:90837630-90853986
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:322)
CpG islands
(count:183)
Chromatin interactive
region (count:33)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:322 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:90838811-90838957	HepG2	liver:	n/a	n/a
2	ATF1	chr8:90851185-90851416	K562	blood:	n/a	n/a
3	ATF2	chr8:90849017-90849522	GM12878	blood:	n/a	n/a
4	ATF2	chr8:90848887-90849536	GM12878	blood:	n/a	n/a
5	ATF3	chr8:90851178-90851424	K562	blood:	n/a	n/a
6	BATF	chr8:90849099-90849357	GM12878	blood:	n/a	n/a
7	BATF	chr8:90846770-90847078	GM12878	blood:	n/a	n/a
8	BATF	chr8:90849053-90849348	GM12878	blood:	n/a	n/a
9	BCL11A	chr8:90845928-90846150	GM12878	blood:	n/a	n/a
10	BCL11A	chr8:90849030-90849412	GM12878	blood:	n/a	chr8:90849336-90849345
11	BCLAF1	chr8:90848930-90849556	GM12878	blood:	n/a	chr8:90849336-90849345
12	BCLAF1	chr8:90848961-90849387	GM12878	blood:	n/a	chr8:90849336-90849345
13	BHLHE40	chr8:90849020-90849429	GM12878	blood:	n/a	n/a
14	BHLHE40	chr8:90847723-90847926	GM12878	blood:	n/a	n/a
15	BHLHE40	chr8:90848633-90848775	GM12878	blood:	n/a	n/a
16	BHLHE40	chr8:90838425-90838937	GM12878	blood:	n/a	n/a
17	BRCA1	chr8:90838179-90838327	GM12878	blood:	n/a	n/a
18	CEBPB	chr8:90849049-90849979	IMR90	lung:	n/a	n/a
19	CEBPB	chr8:90851098-90851448	IMR90	lung:	n/a	chr8:90851263-90851274
20	CEBPB	chr8:90851070-90851480	K562	blood:	n/a	chr8:90851263-90851274
21	CEBPB	chr8:90851097-90851459	HepG2	liver:	n/a	chr8:90851263-90851274
22	CEBPB	chr8:90851147-90851523	HCT-116	colon:	n/a	chr8:90851263-90851274
23	CEBPB	chr8:90851126-90851467	ECC-1	luminal epithelium:	n/a	chr8:90851263-90851274
24	CEBPB	chr8:90851138-90851520	A549	lung:	n/a	chr8:90851263-90851274
25	CEBPB	chr8:90848916-90849612	GM12878	blood:	n/a	n/a
26	CEBPB	chr8:90851042-90851475	MCF-7	breast:	n/a	chr8:90851263-90851274
27	CEBPB	chr8:90851107-90851445	K562	blood:	n/a	chr8:90851263-90851274
28	CEBPB	chr8:90851110-90851462	Hela-S3	cervix:	n/a	chr8:90851263-90851274
29	CEBPB	chr8:90853556-90854111	K562	blood:	n/a	chr8:90853683-90853694
30	CEBPB	chr8:90851146-90851433	ECC-1	luminal epithelium:	n/a	chr8:90851263-90851274
31	CEBPB	chr8:90851043-90851459	MCF-7	breast:	n/a	chr8:90851263-90851274
32	CEBPB	chr8:90851019-90851564	HCT-116	colon:	n/a	chr8:90851263-90851274
33	CEBPB	chr8:90851068-90851580	A549	lung:	n/a	chr8:90851263-90851274
34	CEBPB	chr8:90851081-90851440	H1-hESC	embryonic stem cell:	n/a	chr8:90851263-90851274
35	CEBPB	chr8:90840694-90841001	HepG2	liver:	n/a	n/a
36	CEBPB	chr8:90840754-90840941	A549	lung:	n/a	n/a
37	CEBPB	chr8:90849188-90849894	A549	lung:	n/a	n/a
38	CEBPB	chr8:90853575-90854197	A549	lung:	n/a	chr8:90853683-90853694
39	CEBPB	chr8:90853557-90854240	IMR90	lung:	n/a	chr8:90853683-90853694
40	CEBPB	chr8:90851081-90851468	K562	blood:	n/a	chr8:90851263-90851274
41	CEBPB	chr8:90851127-90851473	A549	lung:	n/a	chr8:90851263-90851274
42	CEBPB	chr8:90853894-90854202	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr8:90853564-90853761	HepG2	liver:	n/a	chr8:90853683-90853694
44	CEBPB	chr8:90853593-90853853	K562	blood:	n/a	chr8:90853683-90853694
45	CHD1	chr8:90848237-90848481	GM12878	blood:	n/a	n/a
46	CHD1	chr8:90848953-90849648	GM12878	blood:	n/a	chr8:90848981-90848991
47	CHD1	chr8:90847707-90847789	GM12878	blood:	n/a	n/a
48	CHD2	chr8:90845833-90846340	GM12878	blood:	n/a	n/a
49	CHD2	chr8:90848560-90848825	GM12878	blood:	n/a	n/a
50	CHD2	chr8:90849073-90849784	GM12878	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:90847772-90847822	MCF10A-Er-Src	breast:	n/a
2	chr8:90849014-90849064	GM12878	blood:	n/a
3	chr8:90837663-90837713	NHDF-neo	bronchial:	n/a
4	chr8:90837663-90837713	T-47D	breast:	n/a
5	chr8:90849014-90849064	PFSK-1	brain:	n/a
6	chr8:90849014-90849064	HNPCEpiC	eye:	n/a
7	chr8:90847772-90847822	SK-N-SH	brain:	n/a
8	chr8:90837663-90837713	HUVEC	blood vessel:	n/a
9	chr8:90849014-90849064	HCPEpiC	choroid plexus:	n/a
10	chr8:90847772-90847822	HIPEpiC	eye:	n/a
11	chr8:90847772-90847822	GM19239	blood:	n/a
12	chr8:90849014-90849064	HAEpiC	amniotic membrane:	n/a
13	chr8:90837663-90837713	GM12892	blood:	n/a
14	chr8:90837663-90837713	MCF10A-Er-Src	breast:	n/a
15	chr8:90837663-90837713	Hela-S3	cervix:	n/a
16	chr8:90849014-90849064	H1-hESC	embryonic stem cell:	embryo
17	chr8:90847772-90847822	HNPCEpiC	eye:	n/a
18	chr8:90849014-90849064	NT2-D1	testis:	n/a
19	chr8:90837663-90837713	AG09319	gingival:	n/a
20	chr8:90849014-90849064	NB4	blood:	n/a
21	chr8:90849014-90849064	HMEC	breast:	n/a
22	chr8:90837663-90837713	Caco-2	colon:	n/a
23	chr8:90837663-90837713	GM12878	blood:	n/a
24	chr8:90847772-90847822	NT2-D1	testis:	n/a
25	chr8:90847772-90847822	HUVEC	blood vessel:	n/a
26	chr8:90837663-90837713	ECC-1	luminal epithelium:	n/a
27	chr8:90849014-90849064	AG09309	skin:	n/a
28	chr8:90837663-90837713	RPTEC	kidney:	n/a
29	chr8:90849014-90849064	SAEC	small airway:	n/a
30	chr8:90849014-90849064	HPAEpiC	pulmonary alveolar:	n/a
31	chr8:90847772-90847822	NHDF-neo	bronchial:	n/a
32	chr8:90847772-90847822	HEK293	kidney:	embryo
33	chr8:90847772-90847822	AG04450	lung:	fetal
34	chr8:90849014-90849064	PrEC	prostate:	n/a
35	chr8:90849014-90849064	NHBE	bronchial:	n/a
36	chr8:90849014-90849064	Jurkat	blood:	n/a
37	chr8:90847772-90847822	GM12878	blood:	n/a
38	chr8:90849014-90849064	HepG2	liver:	n/a
39	chr8:90849014-90849064	MCF-7	breast:	n/a
40	chr8:90849014-90849064	HRCEpiC	kidney:	n/a
41	chr8:90847772-90847822	A549	lung:	n/a
42	chr8:90847772-90847822	HepG2	liver:	n/a
43	chr8:90837663-90837713	HRCEpiC	kidney:	n/a
44	chr8:90837663-90837713	HMEC	breast:	n/a
45	chr8:90849014-90849064	HEEpiC	esophagus:	n/a
46	chr8:90849014-90849064	AG09319	gingival:	n/a
47	chr8:90849014-90849064	HUVEC	blood vessel:	n/a
48	chr8:90837663-90837713	AG04449	skin:	fetal
49	chr8:90837663-90837713	HCF	heart:	n/a
50	chr8:90849014-90849064	SKMC	muscle:	n/a

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:90800222..90801982-chr8:90840675..90842723,2	MCF-7	breast:
2	chr8:90838601..90840941-chr8:90843850..90846321,2	MCF-7	breast:
3	chr8:90848881..90850770-chr8:90855549..90858442,2	MCF-7	breast:
4	chr8:90835990..90838723-chr8:90850259..90852353,2	K562	blood:
5	chr8:90835853..90837817-chr8:90838818..90840749,2	MCF-7	breast:
6	chr8:90835014..90836804-chr8:90836875..90838600,2	K562	blood:
7	chr8:90841193..90842876-chr8:90844123..90846004,2	MCF-7	breast:
8	chr8:90838136..90841638-chr8:90842560..90845111,3	K562	blood:
9	chr1:153928343..153930810-chr8:90845808..90848291,2	MCF-7	breast:
10	chr8:90816818..90818597-chr8:90852863..90855109,2	MCF-7	breast:
11	chr8:90844734..90847246-chr8:90847760..90849982,2	MCF-7	breast:
12	chr8:90836699..90839189-chr8:90853198..90855476,2	MCF-7	breast:
13	chr8:90850950..90853766-chr8:90995447..90997024,2	K562	blood:
14	chr8:90841193..90842876-chr8:90844123..90846004,2	MCF-7	breast:
15	chr8:90835454..90837187-chr8:90837338..90840296,2	MCF-7	breast:
16	chr8:90842015..90844808-chr8:90846350..90848041,2	MCF-7	breast:
17	chr8:90842015..90844808-chr8:90846350..90848041,2	MCF-7	breast:
18	chr8:90853874..90856166-chr8:90995472..90997827,2	MCF-7	breast:
19	chr8:90838578..90843611-chr8:90912392..90915640,4	MCF-7	breast:
20	chr8:90845301..90847765-chr8:90850348..90853325,2	MCF-7	breast:
21	chr8:90844504..90846119-chr8:90995493..90997687,2	MCF-7	breast:
22	chr8:90843753..90846365-chr8:90914514..90916042,2	MCF-7	breast:
23	chr8:90824515..90827081-chr8:90836313..90840458,3	MCF-7	breast:
24	chr8:90845301..90847765-chr8:90850348..90853325,2	MCF-7	breast:
25	chr8:90852737..90854940-chr8:90914150..90915970,2	MCF-7	breast:
26	chr8:90836699..90839189-chr8:90853198..90855476,2	MCF-7	breast:
27	chr8:90844734..90847246-chr8:90847760..90849982,2	MCF-7	breast:
28	chr8:90852614..90855258-chr8:90856891..90858844,2	MCF-7	breast:
29	chr8:90768306..90772219-chr8:90848541..90851274,3	MCF-7	breast:
30	chr8:90841090..90842981-chr8:90920708..90922317,2	MCF-7	breast:
31	chr8:90838601..90840941-chr8:90843850..90846321,2	MCF-7	breast:
32	chr8:90737986..90738708-chr8:90849422..90850036,2	MCF-7	breast:
33	chr8:90838136..90841638-chr8:90842560..90845111,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NBN-5	chr8:90838399-90839074	ucscGeneNc_uc003yed_1

No data

Variant related genes	Relation type
COX6B1P6	TF binding region
COX6B1P6	CpG island
ENSG00000164823	chromatin interactions
ENSG00000207359	chromatin interactions
ENSG00000104312	chromatin interactions
ENSG00000104320	chromatin interactions
ENSG00000251136	chromatin interactions
ENSG00000160741	chromatin interactions
ENSG00000253349	chromatin interactions

Extended variants
information (count: 561 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:561 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs374957	chr8:90837630-90837631	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs540622277	chr8:90837663-90837664	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs370564284	chr8:90837664-90837665	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs546292654	chr8:90837674-90837675	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs375327928	chr8:90837675-90837676	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs16900885	chr8:90837691-90837692	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs42481	chr8:90837714-90837715	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs375863225	chr8:90837724-90837725	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs77614906	chr8:90837725-90837726	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs16900888	chr8:90837747-90837748	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs562106819	chr8:90837749-90837750	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs182681858	chr8:90837758-90837759	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs570714325	chr8:90837820-90837821	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs34039988	chr8:90837827-90837828	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs551012954	chr8:90837828-90837829	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs186958405	chr8:90837868-90837869	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs192221548	chr8:90837869-90837870	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs548902145	chr8:90837894-90837895	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs567480927	chr8:90837903-90837904	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs149906638	chr8:90837920-90837921	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs556520258	chr8:90837953-90837954	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs73696806	chr8:90837978-90837979	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs539852501	chr8:90837990-90837991	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs39517	chr8:90837994-90837995	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs184249146	chr8:90838067-90838068	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs540751439	chr8:90838074-90838075	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs186499290	chr8:90838094-90838095	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs373852939	chr8:90838153-90838154	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs574190081	chr8:90838188-90838189	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs544473309	chr8:90838194-90838195	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs16900910	chr8:90838203-90838204	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs532724749	chr8:90838205-90838206	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs188849367	chr8:90838242-90838243	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs34531272	chr8:90838243-90838244	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs538160217	chr8:90838244-90838245	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs74603465	chr8:90838256-90838257	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs35004759	chr8:90838258-90838259	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs544594175	chr8:90838279-90838280	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs560140194	chr8:90838343-90838344	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs193210991	chr8:90838365-90838366	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs549078110	chr8:90838417-90838418	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
42	rs78437189	chr8:90838444-90838445	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
43	rs16900915	chr8:90838452-90838453	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs550061262	chr8:90838483-90838484	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
45	rs562709282	chr8:90838499-90838500	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
46	rs571558931	chr8:90838551-90838552	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
47	rs538984194	chr8:90838567-90838568	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
48	rs56337634	chr8:90838569-90838570	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs372615932	chr8:90838578-90838579	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
50	rs533999690	chr8:90838592-90838593	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:107)

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
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
Breast cancer	20409316	CNVD
Acute myeloid leukemia	19651601	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Breast cancer	21611746	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:254 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:90828000-90845800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr8:90836400-90837800	Enhancers	Fetal Intestine Large	intestine
3	chr8:90836800-90838200	Enhancers	A549	lung
4	chr8:90836800-90838400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr8:90836800-90839000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr8:90837000-90837800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr8:90837000-90838200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr8:90837000-90838200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr8:90837000-90838200	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr8:90837000-90839000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr8:90837000-90847600	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr8:90837200-90838200	Weak transcription	Pancreas	Pancrea
13	chr8:90837200-90838400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr8:90837200-90844600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr8:90837400-90837800	Enhancers	HepG2	liver
16	chr8:90837400-90838200	Enhancers	Pancreatic Islets	Pancreatic Islet
17	chr8:90837400-90838400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr8:90837600-90838000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr8:90837600-90838000	Weak transcription	Stomach Mucosa	stomach
20	chr8:90837600-90839200	Enhancers	Muscle Satellite Cultured Cells	--
21	chr8:90837800-90838000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr8:90837800-90839000	Weak transcription	HepG2	liver
23	chr8:90837800-90839200	Enhancers	GM12878-XiMat	blood
24	chr8:90837800-90839200	Enhancers	Osteobl	bone
25	chr8:90838000-90838600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr8:90838000-90839000	Enhancers	Stomach Mucosa	stomach
27	chr8:90838000-90839600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr8:90838000-90841000	Enhancers	NHDF-Ad	bronchial
29	chr8:90838200-90838400	Enhancers	Pancreas	Pancrea
30	chr8:90838200-90838600	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr8:90838200-90838600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr8:90838200-90838600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr8:90838200-90839000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr8:90838200-90839000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr8:90838200-90839000	Flanking Active TSS	A549	lung
36	chr8:90838200-90839000	Enhancers	NH-A	brain
37	chr8:90838400-90838600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
38	chr8:90838400-90838800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr8:90838400-90839000	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr8:90838400-90839000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
41	chr8:90838600-90841000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr8:90838800-90841200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr8:90839000-90839200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr8:90839000-90839200	Enhancers	HepG2	liver
45	chr8:90839000-90839400	Enhancers	A549	lung
46	chr8:90839200-90848400	Weak transcription	Osteobl	bone
47	chr8:90839400-90839800	Weak transcription	A549	lung
48	chr8:90839600-90839800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr8:90839600-90840000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr8:90839600-90840000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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