Variant report

Variant	esv34042
Chromosome Location	chr8:11698337-11726817
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2457)
CpG islands
(count:1039)
Chromatin interactive
region (count:51)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2457 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:11720016-11720613	K562	blood:	n/a	n/a
2	ARID3A	chr8:11711460-11711976	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:11710564-11710991	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:11719967-11720499	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:11722303-11722739	HepG2	liver:	n/a	n/a
6	ATF1	chr8:11719934-11720561	K562	blood:	n/a	n/a
7	ATF2	chr8:11724597-11725205	GM12878	blood:	n/a	n/a
8	ATF2	chr8:11718234-11718663	GM12878	blood:	n/a	n/a
9	ATF2	chr8:11724806-11725122	GM12878	blood:	n/a	n/a
10	ATF2	chr8:11718117-11718791	GM12878	blood:	n/a	n/a
11	ATF2	chr8:11716064-11716683	GM12878	blood:	n/a	n/a
12	ATF2	chr8:11704572-11705318	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF3	chr8:11711440-11711869	K562	blood:	n/a	chr8:11711746-11711755
14	ATF3	chr8:11720050-11720523	K562	blood:	n/a	n/a
15	ATF3	chr8:11725467-11725700	K562	blood:	n/a	n/a
16	ATF3	chr8:11711190-11711884	A549	lung:	n/a	chr8:11711746-11711755
17	ATF3	chr8:11711524-11711774	K562	blood:	n/a	chr8:11711746-11711755
18	ATF3	chr8:11725482-11725723	HepG2	liver:	n/a	n/a
19	BACH1	chr8:11720086-11720270	K562	blood:	n/a	n/a
20	BATF	chr8:11718273-11718716	GM12878	blood:	n/a	chr8:11718530-11718541
21	BATF	chr8:11718298-11718610	GM12878	blood:	n/a	chr8:11718530-11718541
22	BCL11A	chr8:11716227-11716542	GM12878	blood:	n/a	n/a
23	BCL11A	chr8:11718244-11718588	GM12878	blood:	n/a	n/a
24	BCL11A	chr8:11716165-11716612	GM12878	blood:	n/a	n/a
25	BCL11A	chr8:11718308-11718637	GM12878	blood:	n/a	n/a
26	BCL3	chr8:11705132-11705635	K562	blood:	n/a	n/a
27	BCL3	chr8:11700687-11701096	K562	blood:	n/a	n/a
28	BCL3	chr8:11725383-11725760	GM12878	blood:	n/a	n/a
29	BCL3	chr8:11725327-11725762	A549	lung:	n/a	n/a
30	BCL3	chr8:11701138-11705117	K562	blood:	n/a	n/a
31	BCL3	chr8:11704974-11705270	GM12878	blood:	n/a	n/a
32	BCL3	chr8:11706000-11706740	GM12878	blood:	n/a	n/a
33	BCL3	chr8:11699609-11700117	A549	lung:	n/a	n/a
34	BCLAF1	chr8:11720126-11720531	K562	blood:	n/a	n/a
35	BCLAF1	chr8:11716093-11716697	GM12878	blood:	n/a	n/a
36	BCLAF1	chr8:11718158-11718703	GM12878	blood:	n/a	n/a
37	BCLAF1	chr8:11718183-11718689	GM12878	blood:	n/a	n/a
38	BCLAF1	chr8:11725364-11725722	GM12878	blood:	n/a	n/a
39	BHLHE40	chr8:11723871-11724307	HepG2	liver:	n/a	n/a
40	BHLHE40	chr8:11701849-11701953	K562	blood:	n/a	n/a
41	BHLHE40	chr8:11726001-11726018	K562	blood:	n/a	n/a
42	BHLHE40	chr8:11706613-11706766	K562	blood:	n/a	n/a
43	BHLHE40	chr8:11711404-11711808	HepG2	liver:	n/a	chr8:11711744-11711760
44	BHLHE40	chr8:11703047-11703271	K562	blood:	n/a	n/a
45	BHLHE40	chr8:11725499-11725699	GM12878	blood:	n/a	n/a
46	BHLHE40	chr8:11718221-11718702	GM12878	blood:	n/a	n/a
47	BHLHE40	chr8:11724911-11725184	K562	blood:	n/a	n/a
48	BHLHE40	chr8:11720032-11720462	HepG2	liver:	n/a	n/a
49	BHLHE40	chr8:11725436-11726052	HepG2	liver:	n/a	n/a
50	BHLHE40	chr8:11711347-11711840	K562	blood:	n/a	chr8:11711744-11711760

(count:1039 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:11710911-11710961	AoSMC	blood vessel:	n/a
2	chr8:11726286-11726336	Jurkat	blood:	n/a
3	chr8:11710911-11710961	AoSMC	blood vessel:	n/a
4	chr8:11726286-11726336	Jurkat	blood:	n/a
5	chr8:11725492-11725542	PANC-1	pancreas:	n/a
6	chr8:11725599-11725649	ProgFib	skin:	n/a
7	chr8:11726043-11726093	AG09319	gingival:	n/a
8	chr8:11723816-11723866	SK-N-MC	brain:	n/a
9	chr8:11725596-11725646	NT2-D1	testis:	n/a
10	chr8:11725104-11725154	SK-N-SH_RA	brain:	n/a
11	chr8:11723816-11723866	SKMC	muscle:	n/a
12	chr8:11724777-11724827	HCM	heart:	n/a
13	chr8:11725306-11725356	LNCaP	prostate:	n/a
14	chr8:11724777-11724827	AG09309	skin:	n/a
15	chr8:11725306-11725356	HCPEpiC	choroid plexus:	n/a
16	chr8:11725599-11725649	GM12892	blood:	n/a
17	chr8:11715284-11715334	LNCaP	prostate:	n/a
18	chr8:11719367-11719417	AG04449	skin:	fetal
19	chr8:11721826-11721876	AG09309	skin:	n/a
20	chr8:11725492-11725542	ovcar-3	ovarian:	n/a
21	chr8:11726043-11726093	SK-N-SH	brain:	n/a
22	chr8:11725492-11725542	AG04449	skin:	fetal
23	chr8:11725596-11725646	SKMC	muscle:	n/a
24	chr8:11726286-11726336	BE2_C	brain:	n/a
25	chr8:11725104-11725154	A549	lung:	n/a
26	chr8:11726094-11726144	HAEpiC	amniotic membrane:	n/a
27	chr8:11723816-11723866	HRE	kidney:	n/a
28	chr8:11725306-11725356	A549	lung:	n/a
29	chr8:11725492-11725542	H1-hESC	embryonic stem cell:	embryo
30	chr8:11725104-11725154	RPTEC	kidney:	n/a
31	chr8:11710911-11710961	H1-hESC	embryonic stem cell:	embryo
32	chr8:11725599-11725649	HEK293	kidney:	embryo
33	chr8:11725104-11725154	AG09319	gingival:	n/a
34	chr8:11717853-11717903	HPAEpiC	pulmonary alveolar:	n/a
35	chr8:11726043-11726093	NH-A	brain:	n/a
36	chr8:11725104-11725154	PrEC	prostate:	n/a
37	chr8:11710911-11710961	LNCaP	prostate:	n/a
38	chr8:11726043-11726093	AG10803	skin:	n/a
39	chr8:11725599-11725649	HCM	heart:	n/a
40	chr8:11725599-11725649	HUVEC	blood vessel:	n/a
41	chr8:11725596-11725646	HCF	heart:	n/a
42	chr8:11726286-11726336	T-47D	breast:	n/a
43	chr8:11723816-11723866	HRCEpiC	kidney:	n/a
44	chr8:11725596-11725646	BJ	skin:	n/a
45	chr8:11725492-11725542	HCM	heart:	n/a
46	chr8:11725306-11725356	HEK293	kidney:	embryo
47	chr8:11726043-11726093	H1-hESC	embryonic stem cell:	embryo
48	chr8:11726286-11726336	AG09319	gingival:	n/a
49	chr8:11725306-11725356	PFSK-1	brain:	n/a
50	chr8:11726094-11726144	GM06990	blood:	n/a

(count:51 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:11658317..11661287-chr8:11697246..11700186,2	K562	blood:
2	chr8:11718857..11721432-chr8:11753489..11755957,2	K562	blood:
3	chr8:11709901..11713097-chr8:11718255..11721625,5	MCF-7	breast:
4	chr8:11625866..11628884-chr8:11724599..11727626,3	MCF-7	breast:
5	chr8:11662566..11665636-chr8:11705504..11707081,3	K562	blood:
6	chr8:11706290..11708186-chr8:11724044..11726922,3	MCF-7	breast:
7	chr8:11695667..11699183-chr8:11720606..11722768,3	K562	blood:
8	chr8:11695946..11697771-chr8:11722616..11724742,2	MCF-7	breast:
9	chr8:11626986..11628635-chr8:11724070..11726191,2	K562	blood:
10	chr8:11625966..11628578-chr8:11704558..11706433,2	MCF-7	breast:
11	chr8:11710836..11712408-chr8:11724380..11726355,2	MCF-7	breast:
12	chr8:11717376..11719253-chr8:11741735..11744320,2	K562	blood:
13	chr8:11701610..11705224-chr8:11724505..11726759,3	MCF-7	breast:
14	chr8:11699877..11702780-chr8:11758303..11760780,3	K562	blood:
15	chr8:11715679..11717977-chr8:11719165..11721934,2	MCF-7	breast:
16	chr11:62608950..62609596-chr8:11725047..11725738,2	HCT-116	colon:
17	chr8:11710197..11714536-chr8:11724997..11727273,4	K562	blood:
18	chr8:11708512..11715317-chr8:11723234..11727095,9	MCF-7	breast:
19	chr8:11717778..11719934-chr8:11735920..11738113,2	MCF-7	breast:
20	chr12:90102840..90103619-chr8:11725166..11725791,2	HCT-116	colon:
21	chr8:11701610..11705224-chr8:11724505..11726759,3	MCF-7	breast:
22	chr8:11701711..11703998-chr8:11723479..11725596,2	K562	blood:
23	chr8:11701923..11705144-chr8:11709953..11712815,3	K562	blood:
24	chr8:11689387..11691686-chr8:11696731..11698715,2	K562	blood:
25	chr8:11706164..11707709-chr8:11709253..11711783,2	K562	blood:
26	chr8:11708512..11715317-chr8:11723234..11727095,9	MCF-7	breast:
27	chr8:11706164..11707709-chr8:11709253..11711783,2	K562	blood:
28	chr16:87902576..87903306-chr8:11724748..11725674,2	Hela-S3	cervix:
29	chr8:11706290..11708186-chr8:11724044..11726922,3	MCF-7	breast:
30	chr8:11678607..11680636-chr8:11724388..11726584,2	MCF-7	breast:
31	chr8:11659426..11661474-chr8:11724613..11726870,3	MCF-7	breast:
32	chr8:11658864..11661745-chr8:11724576..11726431,3	MCF-7	breast:
33	chr8:11718467..11721222-chr8:11754378..11756104,3	K562	blood:
34	chr8:11695667..11699183-chr8:11720606..11722768,3	K562	blood:
35	chr8:11701711..11703998-chr8:11723479..11725596,2	K562	blood:
36	chr8:11693196..11696107-chr8:11696780..11702016,6	K562	blood:
37	chr8:11708825..11713035-chr8:11718721..11724039,7	MCF-7	breast:
38	chr8:11710201..11712259-chr8:11713212..11714755,2	MCF-7	breast:
39	chr8:11710197..11714536-chr8:11724997..11727273,4	K562	blood:
40	chr8:11724192..11726313-chr8:11753136..11754724,2	MCF-7	breast:
41	chr8:11708825..11713035-chr8:11718721..11724039,7	MCF-7	breast:
42	chr8:11710005..11711598-chr8:11715052..11717778,2	MCF-7	breast:
43	chr8:11664303..11666890-chr8:11705423..11707941,2	MCF-7	breast:
44	chr8:11709901..11713097-chr8:11718255..11721625,5	MCF-7	breast:
45	chr8:11701923..11705144-chr8:11709953..11712815,3	K562	blood:
46	chr8:11710836..11712408-chr8:11724380..11726355,2	MCF-7	breast:
47	chr8:11665243..11667469-chr8:11710761..11712863,3	MCF-7	breast:
48	chr8:11714135..11717431-chr8:11717814..11720890,3	K562	blood:
49	chr8:11697890..11700465-chr8:11711516..11714369,2	K562	blood:
50	chr8:11664874..11667348-chr8:11701152..11702795,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-297N6.4.1-2	chr8:11703663-11703900	ENSG00000269899.1
2	lnc-FDFT1-1	chr8:11701603-11702070	expReg_chr8_457_+

No data

Variant related genes	Relation type
CTSB	TF binding region
ENSG00000269899	TF binding region
CTSB	CpG island
ENSG00000269899	CpG island
ENSG00000154328	chromatin interactions
ENSG00000269899	chromatin interactions
ENSG00000255144	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000255046	chromatin interactions
ENSG00000079459	chromatin interactions
ENSG00000103257	chromatin interactions
ENSG00000164733	chromatin interactions
ENSG00000070961	chromatin interactions

Extended variants
information (count: 2351 )
Associated
traits (count: 140 )

Variant overlapped rSNPs/rCNVs (count:2351 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1293330	chr8:11698337-11698338	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs190053117	chr8:11698338-11698339	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs565719839	chr8:11698339-11698340	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs370831741	chr8:11698355-11698356	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs539467309	chr8:11698365-11698366	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs374187037	chr8:11698369-11698370	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs77467456	chr8:11698379-11698380	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs566811843	chr8:11698410-11698411	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs534051684	chr8:11698417-11698418	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs555276621	chr8:11698420-11698421	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs573753691	chr8:11698432-11698433	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs1293331	chr8:11698436-11698437	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs556274867	chr8:11698446-11698447	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs61394300	chr8:11698464-11698465	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs545050758	chr8:11698469-11698470	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs561968471	chr8:11698476-11698477	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs548131981	chr8:11698503-11698504	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs567984244	chr8:11698546-11698547	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs560107104	chr8:11698558-11698559	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs527988985	chr8:11698563-11698564	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs565374869	chr8:11698564-11698565	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs543274911	chr8:11698568-11698569	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs555276939	chr8:11698578-11698579	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs543453470	chr8:11698588-11698589	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs561337923	chr8:11698596-11698597	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs531964211	chr8:11698603-11698604	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs550373107	chr8:11698656-11698657	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs569020264	chr8:11698659-11698660	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs193078433	chr8:11698663-11698664	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs551404292	chr8:11698665-11698666	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs537319915	chr8:11698668-11698669	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs533865916	chr8:11698669-11698670	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs142560364	chr8:11698716-11698717	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs529384828	chr8:11698719-11698720	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs1296028	chr8:11698747-11698748	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
36	rs561126368	chr8:11698753-11698754	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs386722322	chr8:11698765-11698766	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs577758005	chr8:11698787-11698788	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs73209014	chr8:11698790-11698791	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs150990707	chr8:11698805-11698806	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs386722323	chr8:11698808-11698809	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs576538969	chr8:11698809-11698810	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs77706396	chr8:11698811-11698812	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs561651837	chr8:11698813-11698814	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs531907725	chr8:11698814-11698815	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs544070664	chr8:11698815-11698816	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs565437222	chr8:11698816-11698817	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs533062852	chr8:11698817-11698818	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs559146438	chr8:11698820-11698821	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs386722325	chr8:11698822-11698823	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:140)

Disease	PMID	Source
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
Prostate cancer	16573809	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Developmental disorder	20461109	CNVD
abnormal development	18461090	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Gastric cancer	21811585	CNVD
Colorectal cancer	16774939	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cancer	20164919	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:2049 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:11667000-11711000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr8:11669400-11708000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr8:11671400-11701400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr8:11675200-11707000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr8:11675800-11712600	Strong transcription	Dnd41	blood
6	chr8:11676200-11704800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
7	chr8:11677000-11705200	Strong transcription	HUES48 Cell Line	embryonic stem cell
8	chr8:11677200-11704400	Strong transcription	H9 Cell Line	embryonic stem cell
9	chr8:11677600-11702000	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr8:11677600-11702000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr8:11677600-11703200	Strong transcription	ES-I3 Cell Line	embryonic stem cell
12	chr8:11677600-11708200	Strong transcription	Cortex derived primary cultured neurospheres	brain
13	chr8:11677600-11710600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr8:11677600-11711800	Strong transcription	Fetal Brain Female	brain
15	chr8:11677800-11706600	Strong transcription	NHLF	lung
16	chr8:11678000-11707400	Strong transcription	HUES64 Cell Line	embryonic stem cell
17	chr8:11678200-11704000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr8:11678200-11704400	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr8:11678200-11704600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr8:11678200-11705200	Strong transcription	HUES6 Cell Line	embryonic stem cell
21	chr8:11678200-11705200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
22	chr8:11678200-11706800	Strong transcription	H1 Cell Line	embryonic stem cell
23	chr8:11678400-11704000	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr8:11678400-11704400	Strong transcription	GM12878-XiMat	blood
25	chr8:11678400-11705600	Strong transcription	Fetal Muscle Trunk	muscle
26	chr8:11678400-11706400	Strong transcription	Sigmoid Colon	Sigmoid Colon
27	chr8:11678600-11705400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr8:11678600-11708600	Strong transcription	HUVEC	blood vessel
29	chr8:11679000-11702200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr8:11679000-11705200	Strong transcription	iPS-15b Cell Line	embryonic stem cell
31	chr8:11679000-11715200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
32	chr8:11679200-11698800	Strong transcription	Rectal Mucosa Donor 31	rectum
33	chr8:11679200-11710400	Strong transcription	NHDF-Ad	bronchial
34	chr8:11679200-11710800	Strong transcription	Fetal Stomach	stomach
35	chr8:11679400-11705600	Strong transcription	Fetal Lung	lung
36	chr8:11679600-11704200	Strong transcription	K562	blood
37	chr8:11680400-11706600	Strong transcription	HepG2	liver
38	chr8:11682200-11713000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
39	chr8:11682400-11712600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr8:11683000-11713200	Strong transcription	Primary B cells from peripheral blood	blood
41	chr8:11683200-11698800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr8:11683200-11698800	Strong transcription	Muscle Satellite Cultured Cells	--
43	chr8:11683200-11698800	Strong transcription	Rectal Mucosa Donor 29	rectum
44	chr8:11683200-11706600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr8:11683200-11710000	Strong transcription	NH-A	brain
46	chr8:11683400-11699000	Strong transcription	Brain Anterior Caudate	brain
47	chr8:11683400-11703400	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr8:11683400-11711600	Strong transcription	Brain Germinal Matrix	brain
49	chr8:11683600-11708600	Strong transcription	Primary hematopoietic stem cells	blood
50	chr8:11683600-11712600	Strong transcription	Primary neutrophils fromperipheralblood	blood

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