Variant report

Variant	nsv891188
Chromosome Location	chr8:92110936-92191011
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:295)
CpG islands
(count:488)
Chromatin interactive
region (count:36)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:295 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:92130895-92131095	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:92112093-92112404	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:92119585-92120834	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:92121937-92122001	HepG2	liver:	n/a	n/a
5	ATF1	chr8:92126805-92126814	K562	blood:	n/a	n/a
6	ATF2	chr8:92157649-92158115	GM12878	blood:	n/a	n/a
7	BACH1	chr8:92130210-92130270	H1-hESC	embryonic stem cell:	n/a	n/a
8	BHLHE40	chr8:92119659-92120741	HepG2	liver:	n/a	n/a
9	BHLHE40	chr8:92120097-92120425	HepG2	liver:	n/a	n/a
10	CEBPB	chr8:92123908-92124201	HepG2	liver:	n/a	n/a
11	CEBPB	chr8:92148653-92148976	IMR90	lung:	n/a	chr8:92148804-92148815
12	CEBPB	chr8:92120050-92120860	HepG2	liver:	n/a	chr8:92120199-92120211
13	CEBPB	chr8:92152343-92152575	HepG2	liver:	n/a	chr8:92152445-92152458 chr8:92152447-92152456 chr8:92152447-92152456 chr8:92152445-92152458 chr8:92152447-92152456 chr8:92152447-92152456 chr8:92152447-92152458 chr8:92152445-92152456 chr8:92152447-92152458
14	CEBPB	chr8:92148613-92148967	MCF-7	breast:	n/a	chr8:92148804-92148815
15	CEBPB	chr8:92130918-92131377	IMR90	lung:	n/a	n/a
16	CEBPB	chr8:92148672-92148965	HepG2	liver:	n/a	chr8:92148804-92148815
17	CEBPB	chr8:92119569-92119750	HepG2	liver:	n/a	n/a
18	CEBPB	chr8:92148641-92148988	K562	blood:	n/a	chr8:92148804-92148815
19	CEBPB	chr8:92120574-92120772	IMR90	lung:	n/a	n/a
20	CEBPB	chr8:92164320-92164536	A549	lung:	n/a	n/a
21	CEBPB	chr8:92148557-92148979	MCF-7	breast:	n/a	chr8:92148804-92148815
22	CEBPB	chr8:92152325-92152560	IMR90	lung:	n/a	chr8:92152445-92152458 chr8:92152447-92152456 chr8:92152447-92152456 chr8:92152445-92152458 chr8:92152447-92152456 chr8:92152447-92152456 chr8:92152447-92152458 chr8:92152445-92152456 chr8:92152447-92152458
23	CHD2	chr8:92179540-92179627	K562	blood:	n/a	n/a
24	CHD2	chr8:92120111-92120465	HepG2	liver:	n/a	n/a
25	CHD2	chr8:92124549-92124557	HepG2	liver:	n/a	n/a
26	CREB1	chr8:92157732-92158202	GM12878	blood:	n/a	n/a
27	CTCF	chr8:92152201-92152298	LNCaP	prostate:	n/a	n/a
28	CTCF	chr8:92120440-92120590	HRPEpiC	eye:	n/a	n/a
29	CTCF	chr8:92120460-92120610	BE2_C	brain:	n/a	n/a
30	CTCF	chr8:92120500-92120650	HMEC	breast:	n/a	n/a
31	CTCF	chr8:92120460-92120610	HCPEpiC	choroid plexus:	n/a	n/a
32	CTCF	chr8:92120518-92120587	Kidney_OC	kidney:	n/a	n/a
33	CTCF	chr8:92120480-92120628	Medullo	brain:	n/a	n/a
34	CTCF	chr8:92115120-92115270	A549	lung:	n/a	n/a
35	CTCF	chr8:92129960-92130110	AG10803	skin:	n/a	n/a
36	CTCF	chr8:92120551-92120591	GM20000	blood:	n/a	n/a
37	CTCF	chr8:92129900-92130050	BJ	skin:	n/a	n/a
38	CTCF	chr8:92120500-92120650	HepG2	liver:	n/a	n/a
39	CTCF	chr8:92120600-92120750	RPTEC	kidney:	n/a	n/a
40	CTCF	chr8:92120312-92120861	MCF-7	breast:	n/a	n/a
41	CTCF	chr8:92120420-92120570	NHDF-neo	bronchial:	n/a	n/a
42	CTCF	chr8:92120546-92120549	K562	blood:	n/a	n/a
43	CTCF	chr8:92120517-92120624	HepG2	liver:	n/a	n/a
44	CTCF	chr8:92129900-92130050	AG04449	skin:	n/a	n/a
45	CTCF	chr8:92175640-92175790	HEEpiC	esophagus:	n/a	n/a
46	CTCF	chr8:92129900-92130050	AG10803	skin:	n/a	n/a
47	CTCF	chr8:92120480-92120630	AG04449	skin:	n/a	n/a
48	CTCF	chr8:92129920-92130070	AG09309	skin:	n/a	n/a
49	CTCF	chr8:92129880-92130030	BJ	skin:	n/a	n/a
50	CTCF	chr8:92120540-92120690	RPTEC	kidney:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:92130025-92130075	Caco-2	colon:	n/a
2	chr8:92114654-92114704	HRPEpiC	eye:	n/a
3	chr8:92114654-92114704	HIPEpiC	eye:	n/a
4	chr8:92113770-92113820	H1-hESC	embryonic stem cell:	embryo
5	chr8:92114654-92114704	Hepatocyte	liver:	n/a
6	chr8:92114654-92114704	HPAEpiC	pulmonary alveolar:	n/a
7	chr8:92177481-92177531	HNPCEpiC	eye:	n/a
8	chr8:92130025-92130075	SK-N-SH	brain:	n/a
9	chr8:92114654-92114704	HepG2	liver:	n/a
10	chr8:92129661-92129711	GM12891	blood:	n/a
11	chr8:92113870-92113920	GM12891	blood:	n/a
12	chr8:92113870-92113920	SAEC	small airway:	n/a
13	chr8:92113770-92113820	SK-N-SH	brain:	n/a
14	chr8:92113770-92113820	MCF-7	breast:	n/a
15	chr8:92130454-92130504	HNPCEpiC	eye:	n/a
16	chr8:92177481-92177531	HL-60	blood:	n/a
17	chr8:92114654-92114704	NT2-D1	testis:	n/a
18	chr8:92130454-92130504	MCF-7	breast:	n/a
19	chr8:92130454-92130504	AG09319	gingival:	n/a
20	chr8:92129661-92129711	SAEC	small airway:	n/a
21	chr8:92114654-92114704	HCT-116	colon:	n/a
22	chr8:92113870-92113920	GM12878	blood:	n/a
23	chr8:92114725-92114775	PrEC	prostate:	n/a
24	chr8:92114654-92114704	AG04450	lung:	fetal
25	chr8:92130025-92130075	NHDF-neo	bronchial:	n/a
26	chr8:92130025-92130075	IMR90	lung:	fetal
27	chr8:92129661-92129711	Hepatocyte	liver:	n/a
28	chr8:92129661-92129711	NH-A	brain:	n/a
29	chr8:92113770-92113820	MCF10A-Er-Src	breast:	n/a
30	chr8:92177481-92177531	ovcar-3	ovarian:	n/a
31	chr8:92130454-92130504	HEK293	kidney:	embryo
32	chr8:92114654-92114704	AG04449	skin:	fetal
33	chr8:92130025-92130075	K562	blood:	n/a
34	chr8:92177481-92177531	K562	blood:	n/a
35	chr8:92130454-92130504	CMK	blood:	n/a
36	chr8:92114725-92114775	NH-A	brain:	n/a
37	chr8:92113770-92113820	GM12878	blood:	n/a
38	chr8:92177481-92177531	HRPEpiC	eye:	n/a
39	chr8:92129661-92129711	NHDF-neo	bronchial:	n/a
40	chr8:92129661-92129711	HRPEpiC	eye:	n/a
41	chr8:92177481-92177531	AG10803	skin:	n/a
42	chr8:92129661-92129711	LNCaP	prostate:	n/a
43	chr8:92113870-92113920	HCM	heart:	n/a
44	chr8:92177481-92177531	PFSK-1	brain:	n/a
45	chr8:92114725-92114775	U87	brain:	n/a
46	chr8:92113770-92113820	AG10803	skin:	n/a
47	chr8:92129661-92129711	HL-60	blood:	n/a
48	chr8:92130025-92130075	PrEC	prostate:	n/a
49	chr8:92130025-92130075	Hela-S3	cervix:	n/a
50	chr8:92113770-92113820	IMR90	lung:	fetal

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:92120884..92123955-chr8:92135517..92137332,3	K562	blood:
2	chr8:92148959..92151184-chr8:92158932..92161122,2	K562	blood:
3	chr8:92110691..92113252-chr8:92118062..92119956,2	K562	blood:
4	chr8:92155872..92157525-chr8:92209191..92211411,2	K562	blood:
5	chr8:92110951..92113555-chr8:92117926..92119500,2	MCF-7	breast:
6	chr8:92098468..92101361-chr8:92119773..92121850,2	K562	blood:
7	chr8:92104591..92107005-chr8:92111374..92113896,5	MCF-7	breast:
8	chr8:92081085..92084002-chr8:92118821..92120627,2	MCF-7	breast:
9	chr8:92148959..92151184-chr8:92158932..92161122,2	K562	blood:
10	chr8:92120202..92121198-chr8:92265328..92266332,4	MCF-7	breast:
11	chr8:92119859..92121552-chr8:92126272..92127780,2	K562	blood:
12	chr8:92144011..92145737-chr8:92157940..92159530,2	K562	blood:
13	chr8:92110664..92112974-chr8:92115701..92118510,3	MCF-7	breast:
14	chr8:92107839..92110534-chr8:92110820..92113788,2	MCF-7	breast:
15	chr8:92150726..92152514-chr8:92154521..92157433,2	MCF-7	breast:
16	chr8:92154407..92157062-chr8:92186719..92188314,2	K562	blood:
17	chr8:92110691..92113252-chr8:92118062..92119956,2	K562	blood:
18	chr8:92110664..92112974-chr8:92115701..92118510,3	MCF-7	breast:
19	chr8:92154407..92157062-chr8:92186719..92188314,2	K562	blood:
20	chr8:92120884..92123342-chr8:92135640..92137332,2	K562	blood:
21	chr8:92185616..92187449-chr8:92210169..92211682,2	K562	blood:
22	chr8:92120448..92121074-chr8:92405403..92406245,2	MCF-7	breast:
23	chr8:92117994..92121552-chr8:92125286..92129221,4	K562	blood:
24	chr8:92120884..92123955-chr8:92135517..92137332,3	K562	blood:
25	chr8:92120884..92123342-chr8:92135640..92137332,2	K562	blood:
26	chr8:92052048..92053750-chr8:92131275..92133087,2	K562	blood:
27	chr8:92117994..92121552-chr8:92125286..92129221,4	K562	blood:
28	chr8:92119859..92121552-chr8:92126272..92127780,2	K562	blood:
29	chr8:92119728..92121505-chr8:92405339..92406291,6	MCF-7	breast:
30	chr8:92132436..92135251-chr8:92135477..92137033,2	K562	blood:
31	chr8:92134168..92136932-chr8:92139678..92141512,2	MCF-7	breast:
32	chr8:92120160..92121035-chr8:92355245..92356052,2	MCF-7	breast:
33	chr8:92134168..92136932-chr8:92139678..92141512,2	MCF-7	breast:
34	chr8:92132436..92135251-chr8:92135477..92137033,2	K562	blood:
35	chr8:92110951..92113555-chr8:92117926..92119500,2	MCF-7	breast:
36	chr8:92144011..92145737-chr8:92157940..92159530,2	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OTUD6B-4	chr8:92142987-92143064	NONHSAT127672
2	lnc-OTUD6B-4	chr8:92142582-92142645	NONHSAT127672
3	lnc-OTUD6B-6	chr8:92151489-92151751	NONHSAT127674
4	lnc-OTUD6B-4	chr8:92145338-92145592	NONHSAT127672
5	lnc-OTUD6B-5	chr8:92147909-92147967	NONHSAT127673
6	lnc-TMEM55A-4	chr8:92151335-92151500	ucscGeneNc_uc003yet_1
7	lnc-OTUD6B-5	chr8:92150995-92151423	NONHSAT127673
8	lnc-TMEM55A-4	chr8:92149320-92151226	ucscGeneNc_uc003yet_1
9	lnc-OTUD6B-3	chr8:92114949-92115072	NONHSAT127671
10	lnc-OTUD6B-3	chr8:92136721-92137011	NONHSAT127671

No data

Variant related genes	Relation type
RN7SL777P	TF binding region
ENSG00000253525	TF binding region
LRRC69	TF binding region
RN7SL777P	CpG island
ENSG00000253525	CpG island
LRRC69	CpG island
ENSG00000263888	chromatin interactions
ENSG00000253738	chromatin interactions
ENSG00000155100	chromatin interactions
ENSG00000147606	chromatin interactions
ENSG00000155099	chromatin interactions

Extended variants
information (count: 2223 )
Associated
traits (count: 118 )

Variant overlapped rSNPs/rCNVs (count:2223 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7820904	chr8:92110936-92110937	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs367565545	chr8:92110945-92110946	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs541302633	chr8:92110967-92110968	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs549627726	chr8:92110971-92110972	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs150024945	chr8:92111001-92111002	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs574898555	chr8:92111023-92111024	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs541915009	chr8:92111071-92111072	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs116040990	chr8:92111149-92111150	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs182003310	chr8:92111225-92111226	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs114360395	chr8:92111230-92111231	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs564051738	chr8:92111285-92111286	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs567532938	chr8:92111336-92111337	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs528418014	chr8:92111372-92111373	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs546544758	chr8:92111380-92111381	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs572009087	chr8:92111406-92111407	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs568256241	chr8:92111414-92111415	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs529033578	chr8:92111415-92111416	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs550747610	chr8:92111421-92111422	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs115260238	chr8:92111550-92111551	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs547552937	chr8:92111603-92111604	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs537130988	chr8:92111615-92111616	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs144902337	chr8:92111617-92111618	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs570482468	chr8:92111622-92111623	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs535000431	chr8:92111697-92111698	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs186186496	chr8:92111708-92111709	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs574976851	chr8:92111816-92111817	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs542101737	chr8:92111831-92111832	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs573587527	chr8:92111863-92111864	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs112284645	chr8:92111932-92111933	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs62531560	chr8:92111933-92111934	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs200606889	chr8:92111938-92111939	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs542689162	chr8:92111973-92111974	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs189812965	chr8:92112013-92112014	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs564086903	chr8:92112058-92112059	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs182270390	chr8:92112067-92112068	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs370127500	chr8:92112217-92112218	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs556240384	chr8:92112222-92112223	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs62531561	chr8:92112237-92112238	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs202015783	chr8:92112251-92112252	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs185812209	chr8:92112280-92112281	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs539112298	chr8:92112371-92112372	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs553911260	chr8:92112611-92112612	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs58052832	chr8:92112720-92112721	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs562320192	chr8:92112777-92112778	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs191452842	chr8:92112782-92112783	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs552216808	chr8:92112786-92112787	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs570518658	chr8:92112793-92112794	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs542578645	chr8:92112843-92112844	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs534651042	chr8:92113086-92113087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs368484349	chr8:92113098-92113099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:118)

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
Non-syndromic sensorineural hearing loss	17122850	CNVD
early-passage human iPS cells	21368824	CNVD
Colorectal cancer	21645411	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Gastric cancer	22014070	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:534 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:92083000-92147800	Weak transcription	Spleen	Spleen
2	chr8:92083200-92113200	Weak transcription	Esophagus	oesophagus
3	chr8:92083400-92124400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr8:92083600-92112000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr8:92083600-92113000	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr8:92083600-92114800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr8:92083600-92150800	Weak transcription	Pancreas	Pancrea
8	chr8:92084000-92124600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr8:92084200-92111400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr8:92085000-92125800	Weak transcription	Small Intestine	intestine
11	chr8:92088000-92111600	Strong transcription	HUES64 Cell Line	embryonic stem cell
12	chr8:92091200-92133800	Weak transcription	NHLF	lung
13	chr8:92091800-92137800	Weak transcription	Rectal Smooth Muscle	rectum
14	chr8:92092600-92111000	Weak transcription	HepG2	liver
15	chr8:92092600-92116800	Weak transcription	Brain Hippocampus Middle	brain
16	chr8:92092600-92147800	Weak transcription	Right Ventricle	heart
17	chr8:92092800-92111400	Weak transcription	Brain Substantia Nigra	brain
18	chr8:92092800-92124400	Weak transcription	Brain Cingulate Gyrus	brain
19	chr8:92094200-92125200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
20	chr8:92095200-92124400	Weak transcription	Skeletal Muscle Male	skeletal muscle
21	chr8:92095200-92130800	Weak transcription	HSMMtube	muscle
22	chr8:92095800-92126600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
23	chr8:92096800-92135000	Weak transcription	Hela-S3	cervix
24	chr8:92097200-92127000	Weak transcription	Colon Smooth Muscle	Colon
25	chr8:92097400-92126400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
26	chr8:92097400-92130800	Weak transcription	Osteobl	bone
27	chr8:92097400-92146200	Weak transcription	Psoas Muscle	Psoas
28	chr8:92098000-92111200	Weak transcription	Brain Germinal Matrix	brain
29	chr8:92098200-92124600	Weak transcription	HUVEC	blood vessel
30	chr8:92098600-92122800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
31	chr8:92100000-92111200	Strong transcription	Primary T cells fromperipheralblood	blood
32	chr8:92100400-92112200	Weak transcription	Stomach Mucosa	stomach
33	chr8:92100400-92115000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr8:92100800-92130800	Weak transcription	Muscle Satellite Cultured Cells	--
35	chr8:92101400-92118800	Weak transcription	Fetal Brain Female	brain
36	chr8:92102600-92111400	Weak transcription	Fetal Lung	lung
37	chr8:92102600-92114800	Weak transcription	NH-A	brain
38	chr8:92104000-92111600	Strong transcription	HUES6 Cell Line	embryonic stem cell
39	chr8:92104400-92117800	Weak transcription	Brain Angular Gyrus	brain
40	chr8:92104400-92124400	Weak transcription	Gastric	stomach
41	chr8:92104600-92114800	Weak transcription	Skeletal Muscle Female	skeletal muscle
42	chr8:92104600-92116800	Weak transcription	Stomach Smooth Muscle	stomach
43	chr8:92104600-92117000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
44	chr8:92104600-92126000	Weak transcription	Fetal Intestine Large	intestine
45	chr8:92104600-92129600	Weak transcription	Brain Anterior Caudate	brain
46	chr8:92104800-92111200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr8:92104800-92112200	Weak transcription	Colonic Mucosa	Colon
48	chr8:92104800-92115000	Weak transcription	Aorta	Aorta
49	chr8:92104800-92124400	Weak transcription	Brain Inferior Temporal Lobe	brain
50	chr8:92104800-92124400	Weak transcription	Ovary	ovary

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