Variant report

Variant	esv3389294
Chromosome Location	chr8:131027670-131029918
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:762)
CpG islands
(count:305)
Chromatin interactive
region (count:17)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:762 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:131028825-131028876	K562	blood:	n/a	n/a
2	ARID3A	chr8:131027514-131028077	K562	blood:	n/a	n/a
3	ATF2	chr8:131027340-131027895	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr8:131027349-131027901	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr8:131027039-131028066	A549	lung:	n/a	chr8:131027168-131027181
6	BACH1	chr8:131027559-131027732	K562	blood:	n/a	n/a
7	BACH1	chr8:131027416-131028151	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr8:131027402-131027674	GM12878	blood:	n/a	n/a
9	BCL3	chr8:131026788-131028063	A549	lung:	n/a	chr8:131027125-131027134
10	BCL3	chr8:131027367-131028192	A549	lung:	n/a	n/a
11	BCLAF1	chr8:131027444-131027824	GM12878	blood:	n/a	n/a
12	BHLHE40	chr8:131028648-131028895	GM12878	blood:	n/a	chr8:131028677-131028693 chr8:131028666-131028682 chr8:131028674-131028690
13	BHLHE40	chr8:131028620-131029126	K562	blood:	n/a	chr8:131028677-131028693 chr8:131029009-131029025 chr8:131028666-131028682 chr8:131028674-131028690
14	BHLHE40	chr8:131027087-131028336	K562	blood:	n/a	chr8:131028299-131028315
15	BHLHE40	chr8:131027293-131027756	GM12878	blood:	n/a	n/a
16	BRCA1	chr8:131027519-131027787	H1-hESC	embryonic stem cell:	n/a	n/a
17	BRCA1	chr8:131029175-131029192	Hela-S3	cervix:	n/a	n/a
18	CBX3	chr8:131027210-131028265	K562	blood:	n/a	n/a
19	CBX3	chr8:131027398-131027948	K562	blood:	n/a	n/a
20	CCNT2	chr8:131027381-131029199	K562	blood:	n/a	n/a
21	CEBPB	chr8:131027422-131027784	K562	blood:	n/a	n/a
22	CEBPB	chr8:131027221-131027722	K562	blood:	n/a	n/a
23	CEBPB	chr8:131027182-131027813	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr8:131028637-131028725	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr8:131029174-131029261	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr8:131027521-131027854	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD1	chr8:131029104-131029241	GM12878	blood:	n/a	n/a
28	CHD1	chr8:131027416-131028122	GM12878	blood:	n/a	n/a
29	CHD1	chr8:131028763-131028862	GM12878	blood:	n/a	chr8:131028822-131028832
30	CHD2	chr8:131028511-131028919	GM12878	blood:	n/a	chr8:131028822-131028832
31	CHD2	chr8:131027950-131029258	Hela-S3	cervix:	n/a	chr8:131028910-131028920 chr8:131028822-131028832
32	CHD2	chr8:131029059-131029416	K562	blood:	n/a	n/a
33	CHD2	chr8:131027749-131027751	HepG2	liver:	n/a	n/a
34	CHD2	chr8:131028781-131028833	H1-hESC	embryonic stem cell:	n/a	chr8:131028822-131028832
35	CHD2	chr8:131028646-131028669	K562	blood:	n/a	n/a
36	CHD2	chr8:131027232-131027733	Hela-S3	cervix:	n/a	n/a
37	CHD2	chr8:131027457-131027956	K562	blood:	n/a	n/a
38	CHD2	chr8:131027493-131027838	H1-hESC	embryonic stem cell:	n/a	n/a
39	CREB1	chr8:131028515-131029342	H1-hESC	embryonic stem cell:	n/a	n/a
40	CREB1	chr8:131028593-131028927	A549	lung:	n/a	n/a
41	CREB1	chr8:131027363-131027823	A549	lung:	n/a	n/a
42	CREB1	chr8:131027339-131027976	H1-hESC	embryonic stem cell:	n/a	n/a
43	CREB1	chr8:131028453-131029439	HepG2	liver:	n/a	n/a
44	CREB1	chr8:131028557-131029007	GM12878	blood:	n/a	n/a
45	CREB1	chr8:131028266-131029154	A549	lung:	n/a	n/a
46	CREB1	chr8:131027481-131027815	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTBP2	chr8:131028567-131029709	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTBP2	chr8:131027378-131028249	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr8:131028140-131028290	Caco-2	colon:	n/a	n/a
50	CTCF	chr8:131027520-131027670	SK-N-SH_RA	brain:	n/a	chr8:131027593-131027611 chr8:131027594-131027610 chr8:131027595-131027608 chr8:131027588-131027609

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:131027724-131027774	GM19239	blood:	n/a
2	chr8:131028990-131029040	T-47D	breast:	n/a
3	chr8:131028990-131029040	PFSK-1	brain:	n/a
4	chr8:131028232-131028282	GM19239	blood:	n/a
5	chr8:131028990-131029040	GM06990	blood:	n/a
6	chr8:131027724-131027774	ProgFib	skin:	n/a
7	chr8:131029139-131029189	NB4	blood:	n/a
8	chr8:131028985-131029035	HL-60	blood:	n/a
9	chr8:131028985-131029035	HMEC	breast:	n/a
10	chr8:131028990-131029040	HCF	heart:	n/a
11	chr8:131028985-131029035	HNPCEpiC	eye:	n/a
12	chr8:131027724-131027774	AG09319	gingival:	n/a
13	chr8:131028232-131028282	HAEpiC	amniotic membrane:	n/a
14	chr8:131027724-131027774	HRPEpiC	eye:	n/a
15	chr8:131028985-131029035	NB4	blood:	n/a
16	chr8:131028990-131029040	HRCEpiC	kidney:	n/a
17	chr8:131027724-131027774	ECC-1	luminal epithelium:	n/a
18	chr8:131027724-131027774	AG04449	skin:	fetal
19	chr8:131028985-131029035	ProgFib	skin:	n/a
20	chr8:131028232-131028282	A549	lung:	n/a
21	chr8:131027724-131027774	HRE	kidney:	n/a
22	chr8:131028985-131029035	HCPEpiC	choroid plexus:	n/a
23	chr8:131028990-131029040	PrEC	prostate:	n/a
24	chr8:131029139-131029189	PANC-1	pancreas:	n/a
25	chr8:131027724-131027774	HL-60	blood:	n/a
26	chr8:131029139-131029189	K562	blood:	n/a
27	chr8:131029139-131029189	SK-N-SH_RA	brain:	n/a
28	chr8:131028985-131029035	H1-hESC	embryonic stem cell:	embryo
29	chr8:131028985-131029035	GM12878	blood:	n/a
30	chr8:131027724-131027774	AoSMC	blood vessel:	n/a
31	chr8:131028990-131029040	HMEC	breast:	n/a
32	chr8:131028990-131029040	MCF10A-Er-Src	breast:	n/a
33	chr8:131027724-131027774	HCF	heart:	n/a
34	chr8:131028990-131029040	SK-N-SH	brain:	n/a
35	chr8:131028232-131028282	PANC-1	pancreas:	n/a
36	chr8:131028232-131028282	GM06990	blood:	n/a
37	chr8:131028232-131028282	HRE	kidney:	n/a
38	chr8:131028990-131029040	HAEpiC	amniotic membrane:	n/a
39	chr8:131029139-131029189	AG10803	skin:	n/a
40	chr8:131028990-131029040	HRE	kidney:	n/a
41	chr8:131028232-131028282	AG09319	gingival:	n/a
42	chr8:131027724-131027774	HCM	heart:	n/a
43	chr8:131028985-131029035	A549	lung:	n/a
44	chr8:131028232-131028282	Jurkat	blood:	n/a
45	chr8:131028985-131029035	PFSK-1	brain:	n/a
46	chr8:131028985-131029035	K562	blood:	n/a
47	chr8:131028985-131029035	Hela-S3	cervix:	n/a
48	chr8:131028232-131028282	Hepatocyte	liver:	n/a
49	chr8:131028232-131028282	GM12891	blood:	n/a
50	chr8:131027724-131027774	SAEC	small airway:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:130950293..130952850-chr8:131027033..131029151,3	MCF-7	breast:
2	chr8:130950488..130952013-chr8:131029373..131031137,2	K562	blood:
3	chr8:130951430..130951975-chr8:131027547..131028096,2	K562	blood:
4	chr8:130908607..130911071-chr8:131026510..131028615,2	MCF-7	breast:
5	chr8:130949943..130953390-chr8:131026093..131029581,5	K562	blood:
6	chr8:130960320..130961292-chr8:131027438..131028472,5	MCF-7	breast:
7	chr8:130981588..130985969-chr8:131024671..131030870,8	K562	blood:
8	chr8:130949293..130953390-chr8:131026261..131028875,4	K562	blood:
9	chr8:130950508..130954142-chr8:131027064..131029855,6	MCF-7	breast:
10	chr8:130981588..130985969-chr8:131027661..131030801,4	K562	blood:
11	chr8:130951528..130952250-chr8:131028470..131029127,2	MCF-7	breast:
12	chr8:131019270..131022496-chr8:131027575..131029857,4	MCF-7	breast:
13	chr20:47442643..47444706-chr8:131026917..131028434,2	MCF-7	breast:
14	chr8:131025540..131027750-chr8:131037896..131040382,2	MCF-7	breast:
15	chr8:130982299..130983095-chr8:131026665..131027754,4	MCF-7	breast:
16	chr8:130951997..130952639-chr8:131027123..131027922,3	MCF-7	breast:
17	chr8:131018416..131020834-chr8:131027208..131028989,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GSDMC-5	chr8:131028853-131028898	NONHSAT129141

No data

Variant related genes	Relation type
FAM49B	TF binding region
FAM49B	CpG island
ENSG00000153310	chromatin interactions
ENSG00000264653	chromatin interactions
ENSG00000124126	chromatin interactions
ENSG00000253720	chromatin interactions

Extended variants
information (count: 73 )
Associated
traits (count: 153 )

Variant overlapped rSNPs/rCNVs (count:73 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs148721175	chr8:131027713-131027714	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs187806942	chr8:131027733-131027734	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs531785378	chr8:131027826-131027827	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs897051	chr8:131027841-131027842	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs376503786	chr8:131027857-131027858	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs549914576	chr8:131027907-131027908	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs529325994	chr8:131027940-131027941	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs547535378	chr8:131027941-131027942	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs192328537	chr8:131027983-131027984	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs539458813	chr8:131027995-131027996	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs552008618	chr8:131028002-131028003	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs184351798	chr8:131028058-131028059	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs570744080	chr8:131028082-131028083	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs116418534	chr8:131028184-131028185	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs568204929	chr8:131028210-131028211	Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs371504809	chr8:131028214-131028215	Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs13253576	chr8:131028331-131028332	Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs13253600	chr8:131028358-131028359	Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs112220482	chr8:131028368-131028369	Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs535541506	chr8:131028389-131028390	Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs553948580	chr8:131028475-131028476	Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs192285422	chr8:131028525-131028526	Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs572028676	chr8:131028547-131028548	Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs545837850	chr8:131028574-131028575	Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs4075727	chr8:131028578-131028579	Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs112125991	chr8:131028590-131028591	Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs576658601	chr8:131028660-131028661	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs543788190	chr8:131028687-131028688	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs562307419	chr8:131028714-131028715	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs575791168	chr8:131028756-131028757	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs543173556	chr8:131028758-131028759	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs547447931	chr8:131028864-131028865	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
33	rs185031455	chr8:131028871-131028872	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
34	rs28490530	chr8:131028872-131028873	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
35	rs35211574	chr8:131028938-131028939	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs551766317	chr8:131028943-131028944	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs569982165	chr8:131028961-131028962	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs150798456	chr8:131029071-131029072	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs549854304	chr8:131029092-131029093	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs568236080	chr8:131029095-131029096	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs377748786	chr8:131029103-131029104	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs527901524	chr8:131029116-131029117	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs535655609	chr8:131029175-131029176	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs553854633	chr8:131029176-131029177	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs572188227	chr8:131029207-131029208	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs539577569	chr8:131029211-131029212	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs12677382	chr8:131029219-131029220	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs557713771	chr8:131029242-131029243	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs576001366	chr8:131029300-131029301	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs114154123	chr8:131029309-131029310	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:153)

Disease	PMID	Source
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
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	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	17603634	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	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
Acute myeloid leukemia	20729466	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
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	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
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Gastric cancer	21528007	CNVD
Breast cancer	22532251	CNVD
Cervical cancer	21062161	CNVD
Cancer	21129771	CNVD
benign familial neonatal convulsions	18472482	CNVD
Breast cancer	16417655	CNVD
Astrocytoma	17387387	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	20814816	CNVD
Colorectal cancer	22486879	CNVD
Breast cancer	17908964	CNVD
Colorectal cancer	20031965	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian cancer	17908964	CNVD
Ovarian cancer	20031965	CNVD
Prostate cancer	20031965	CNVD
Non-small cell lung cancer	17643093	CNVD
Prostate cancer	19242612	CNVD
Colorectal cancer	16774939	CNVD
Malignant melanoma	17260012	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute myeloid leukemia	18379011	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	22048815	CNVD
Colorectal cancer	16912164	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Lung adenocarcinoma	21148746	CNVD
Lung cancer	21911935	CNVD
Breast cancer	20459607	CNVD
Medulloblastoma	19270706	CNVD
Acute myeloid leukemia	19651601	CNVD
Colorectal cancer	21645411	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Colorectal cancer	19455253	CNVD
Glioblastoma multiforme	22286061	CNVD
Colorectal cancer	22860045	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Lung cancer	17925434	CNVD
Non-small cell lung cancer	21829676	CNVD
Prostate cancer	17217626	CNVD
Cancer	17160897	CNVD
Breast cancer	16497871	CNVD
Colorectal cancer	16882699	CNVD
Cystic fibrosis	19273617	CNVD
Chronic stroke	19622162	CNVD
Chordoma	18071362	CNVD
Breast cancer	17850661	CNVD
head and neck squamous cell carcinoma	16740747	CNVD
Gastric cancer	22539939	CNVD
Breast cancer	16272173	CNVD
Uveal melanoma	20484589	CNVD
Ovarian cancer	20844748	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21611746	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:412 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:131012600-131027800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr8:131022200-131028000	Weak transcription	Ovary	ovary
3	chr8:131025400-131027800	Enhancers	Fetal Heart	heart
4	chr8:131026200-131028000	Enhancers	Fetal Brain Male	brain
5	chr8:131026400-131028000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
6	chr8:131026600-131028000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
7	chr8:131026600-131028000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
8	chr8:131026600-131028200	Flanking Active TSS	Primary hematopoietic stem cells	blood
9	chr8:131026600-131028200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
10	chr8:131026600-131028200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
11	chr8:131026800-131027800	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
12	chr8:131026800-131028000	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
13	chr8:131026800-131028000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr8:131026800-131028000	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
15	chr8:131026800-131028000	Flanking Active TSS	A549	lung
16	chr8:131026800-131028200	Flanking Active TSS	Primary B cells from cord blood	blood
17	chr8:131026800-131028200	Flanking Active TSS	GM12878-XiMat	blood
18	chr8:131026800-131028400	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
19	chr8:131026800-131029600	Active TSS	Brain Anterior Caudate	brain
20	chr8:131027000-131027800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr8:131027000-131027800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
22	chr8:131027000-131027800	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
23	chr8:131027000-131027800	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
24	chr8:131027000-131027800	Flanking Active TSS	Fetal Brain Female	brain
25	chr8:131027000-131028000	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
26	chr8:131027000-131028000	Flanking Active TSS	Primary T cells from cord blood	blood
27	chr8:131027000-131028000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
28	chr8:131027000-131028000	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
29	chr8:131027000-131028000	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
30	chr8:131027000-131028000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
31	chr8:131027000-131028000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr8:131027000-131028000	Flanking Active TSS	Brain Angular Gyrus	brain
33	chr8:131027000-131028000	Flanking Active TSS	Duodenum Mucosa	Duodenum
34	chr8:131027000-131028000	Flanking Active TSS	Hela-S3	cervix
35	chr8:131027000-131028000	Flanking Active TSS	HMEC	breast
36	chr8:131027000-131028000	Flanking Active TSS	K562	blood
37	chr8:131027000-131028000	Flanking Active TSS	NHEK	skin
38	chr8:131027000-131028000	Flanking Active TSS	Osteobl	bone
39	chr8:131027000-131028200	Flanking Active TSS	Adipose Nuclei	Adipose
40	chr8:131027000-131028200	Flanking Active TSS	Fetal Muscle Leg	muscle
41	chr8:131027000-131028200	Flanking Active TSS	Stomach Smooth Muscle	stomach
42	chr8:131027000-131029600	Active TSS	Brain Hippocampus Middle	brain
43	chr8:131027000-131029600	Active TSS	Brain Inferior Temporal Lobe	brain
44	chr8:131027200-131027800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr8:131027200-131027800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr8:131027200-131027800	Flanking Active TSS	Fetal Stomach	stomach
47	chr8:131027200-131028000	Flanking Active TSS	Primary T cells fromperipheralblood	blood
48	chr8:131027200-131028000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
49	chr8:131027200-131028200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr8:131027200-131029000	Active TSS	HUES64 Cell Line	embryonic stem cell

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