Variant report

Variant	nsv465809
Chromosome Location	chr8:131005345-131031827
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1489)
CpG islands
(count:613)
Chromatin interactive
region (count:51)
LncRNA
region (count:1)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:1489 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:131012944-131013054	K562	blood:	n/a	n/a
2	ARID3A	chr8:131028825-131028876	K562	blood:	n/a	n/a
3	ARID3A	chr8:131027514-131028077	K562	blood:	n/a	n/a
4	ARID3A	chr8:131009008-131009301	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:131014808-131014920	K562	blood:	n/a	n/a
6	ATF2	chr8:131027349-131027901	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr8:131027340-131027895	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr8:131020655-131021478	GM12878	blood:	n/a	n/a
9	ATF2	chr8:131020554-131021539	GM12878	blood:	n/a	n/a
10	ATF3	chr8:131027039-131028066	A549	lung:	n/a	chr8:131027168-131027181
11	ATF3	chr8:131012045-131012531	K562	blood:	n/a	n/a
12	ATF3	chr8:131008717-131009228	A549	lung:	n/a	n/a
13	ATF3	chr8:131012190-131012473	K562	blood:	n/a	n/a
14	BACH1	chr8:131011443-131012750	K562	blood:	n/a	chr8:131012319-131012333 chr8:131012309-131012323
15	BACH1	chr8:131004552-131005513	K562	blood:	n/a	n/a
16	BACH1	chr8:131011507-131011695	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr8:131027416-131028151	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr8:131006190-131006343	K562	blood:	n/a	n/a
19	BACH1	chr8:131027559-131027732	K562	blood:	n/a	n/a
20	BACH1	chr8:131011927-131012673	H1-hESC	embryonic stem cell:	n/a	chr8:131012319-131012333 chr8:131012309-131012323
21	BACH1	chr8:131009666-131009812	H1-hESC	embryonic stem cell:	n/a	n/a
22	BATF	chr8:131012138-131012431	GM12878	blood:	n/a	chr8:131012322-131012333
23	BATF	chr8:131019146-131019450	GM12878	blood:	n/a	chr8:131019287-131019298
24	BATF	chr8:131020696-131021357	GM12878	blood:	n/a	chr8:131021092-131021100
25	BATF	chr8:131019105-131019438	GM12878	blood:	n/a	chr8:131019287-131019298
26	BATF	chr8:131027402-131027674	GM12878	blood:	n/a	n/a
27	BATF	chr8:131020617-131021490	GM12878	blood:	n/a	chr8:131021092-131021100
28	BCL11A	chr8:131020668-131021346	GM12878	blood:	n/a	chr8:131021095-131021104
29	BCL11A	chr8:131020842-131021300	GM12878	blood:	n/a	chr8:131021095-131021104
30	BCL3	chr8:131007237-131007977	A549	lung:	n/a	chr8:131007498-131007507
31	BCL3	chr8:131027367-131028192	A549	lung:	n/a	n/a
32	BCL3	chr8:131026788-131028063	A549	lung:	n/a	chr8:131027125-131027134
33	BCL3	chr8:131012116-131012428	GM12878	blood:	n/a	n/a
34	BCL3	chr8:131008646-131009374	A549	lung:	n/a	n/a
35	BCL3	chr8:131020912-131021366	GM12878	blood:	n/a	chr8:131021095-131021104
36	BCL3	chr8:131008633-131009320	A549	lung:	n/a	n/a
37	BCL3	chr8:131020745-131021350	GM12878	blood:	n/a	chr8:131021095-131021104
38	BCLAF1	chr8:131027444-131027824	GM12878	blood:	n/a	n/a
39	BCLAF1	chr8:131020592-131021475	GM12878	blood:	n/a	chr8:131021095-131021104
40	BCLAF1	chr8:131020790-131021433	GM12878	blood:	n/a	chr8:131021095-131021104
41	BHLHE40	chr8:131006272-131006906	K562	blood:	n/a	n/a
42	BHLHE40	chr8:131011488-131011691	K562	blood:	n/a	n/a
43	BHLHE40	chr8:131027293-131027756	GM12878	blood:	n/a	n/a
44	BHLHE40	chr8:131012162-131012595	K562	blood:	n/a	n/a
45	BHLHE40	chr8:131017541-131017783	K562	blood:	n/a	chr8:131017662-131017671
46	BHLHE40	chr8:131028648-131028895	GM12878	blood:	n/a	chr8:131028677-131028693 chr8:131028666-131028682 chr8:131028674-131028690
47	BHLHE40	chr8:131004627-131005367	K562	blood:	n/a	n/a
48	BHLHE40	chr8:131020660-131021274	GM12878	blood:	n/a	n/a
49	BHLHE40	chr8:131027087-131028336	K562	blood:	n/a	chr8:131028299-131028315
50	BHLHE40	chr8:131028620-131029126	K562	blood:	n/a	chr8:131028677-131028693 chr8:131029009-131029025 chr8:131028666-131028682 chr8:131028674-131028690

(count:613 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:131011240-131011290	HRPEpiC	eye:	n/a
2	chr8:131008537-131008587	SAEC	small airway:	n/a
3	chr8:131028990-131029040	HepG2	liver:	n/a
4	chr8:131011240-131011290	HRPEpiC	eye:	n/a
5	chr8:131008537-131008587	SAEC	small airway:	n/a
6	chr8:131028990-131029040	HepG2	liver:	n/a
7	chr8:131029139-131029189	HEEpiC	esophagus:	n/a
8	chr8:131028990-131029040	MCF-7	breast:	n/a
9	chr8:131028985-131029035	GM12891	blood:	n/a
10	chr8:131031752-131031802	CMK	blood:	n/a
11	chr8:131028232-131028282	HCT-116	colon:	n/a
12	chr8:131028990-131029040	Hela-S3	cervix:	n/a
13	chr8:131022097-131022147	Caco-2	colon:	n/a
14	chr8:131022097-131022147	NHDF-neo	bronchial:	n/a
15	chr8:131028985-131029035	HepG2	liver:	n/a
16	chr8:131022097-131022147	AG09309	skin:	n/a
17	chr8:131031752-131031802	HRE	kidney:	n/a
18	chr8:131022097-131022147	HUVEC	blood vessel:	n/a
19	chr8:131011240-131011290	HL-60	blood:	n/a
20	chr8:131028990-131029040	HMEC	breast:	n/a
21	chr8:131029139-131029189	H1-hESC	embryonic stem cell:	embryo
22	chr8:131022097-131022147	HepG2	liver:	n/a
23	chr8:131022097-131022147	HIPEpiC	eye:	n/a
24	chr8:131022097-131022147	PrEC	prostate:	n/a
25	chr8:131011240-131011290	H1-hESC	embryonic stem cell:	embryo
26	chr8:131011240-131011290	Jurkat	blood:	n/a
27	chr8:131027724-131027774	HCT-116	colon:	n/a
28	chr8:131011240-131011290	HEK293	kidney:	embryo
29	chr8:131028232-131028282	HIPEpiC	eye:	n/a
30	chr8:131029139-131029189	MCF10A-Er-Src	breast:	n/a
31	chr8:131008537-131008587	HCT-116	colon:	n/a
32	chr8:131031752-131031802	NT2-D1	testis:	n/a
33	chr8:131029139-131029189	HPAEpiC	pulmonary alveolar:	n/a
34	chr8:131025902-131025952	HEEpiC	esophagus:	n/a
35	chr8:131028985-131029035	BJ	skin:	n/a
36	chr8:131008537-131008587	AoSMC	blood vessel:	n/a
37	chr8:131025902-131025952	AG04450	lung:	fetal
38	chr8:131027724-131027774	RPTEC	kidney:	n/a
39	chr8:131031752-131031802	Jurkat	blood:	n/a
40	chr8:131011240-131011290	LNCaP	prostate:	n/a
41	chr8:131028232-131028282	HL-60	blood:	n/a
42	chr8:131022097-131022147	HEK293	kidney:	embryo
43	chr8:131027724-131027774	LNCaP	prostate:	n/a
44	chr8:131029139-131029189	HRPEpiC	eye:	n/a
45	chr8:131028232-131028282	MCF10A-Er-Src	breast:	n/a
46	chr8:131029139-131029189	HUVEC	blood vessel:	n/a
47	chr8:131029139-131029189	HCF	heart:	n/a
48	chr8:131031752-131031802	PANC-1	pancreas:	n/a
49	chr8:131029139-131029189	HepG2	liver:	n/a
50	chr8:131008537-131008587	HL-60	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr8:131007021..131009238-chr8:131011453..131013766,3	MCF-7	breast:
2	chr8:130999286..131001755-chr8:131008650..131010695,2	K562	blood:
3	chr8:130950293..130952850-chr8:131027033..131029151,3	MCF-7	breast:
4	chr8:131014946..131017483-chr8:131021202..131023488,4	MCF-7	breast:
5	chr8:131003704..131005230-chr8:131007280..131008801,2	K562	blood:
6	chr8:131010009..131012187-chr8:131014234..131016988,4	MCF-7	breast:
7	chr8:131008248..131015000-chr8:131026148..131029127,9	K562	blood:
8	chr8:130960320..130961292-chr8:131027438..131028472,5	MCF-7	breast:
9	chr8:130986346..130989213-chr8:131003390..131006806,3	K562	blood:
10	chr8:130987235..130990502-chr8:131006341..131009239,3	MCF-7	breast:
11	chr8:130994958..130999216-chr8:131005349..131009996,7	MCF-7	breast:
12	chr8:131023287..131025131-chr8:131027494..131029690,2	MCF-7	breast:
13	chr8:131020889..131022923-chr8:131027315..131029052,2	MCF-7	breast:
14	chr8:131018416..131020834-chr8:131027208..131028989,2	MCF-7	breast:
15	chr8:131019270..131022496-chr8:131027575..131029857,4	MCF-7	breast:
16	chr8:131028813..131030509-chr8:131031181..131032735,2	MCF-7	breast:
17	chr8:130949293..130953390-chr8:131026261..131028875,4	K562	blood:
18	chr8:130966636..130968344-chr8:131006185..131008673,2	MCF-7	breast:
19	chr8:130951997..130952639-chr8:131027123..131027922,3	MCF-7	breast:
20	chr8:130996585..131001100-chr8:131002410..131006763,8	K562	blood:
21	chr8:130951430..130951975-chr8:131027547..131028096,2	K562	blood:
22	chr8:131009438..131012351-chr8:131027443..131029854,5	MCF-7	breast:
23	chr8:131022542..131024332-chr8:131027331..131030262,2	MCF-7	breast:
24	chr8:131007627..131010623-chr8:131045952..131048257,2	MCF-7	breast:
25	chr8:130981588..130985969-chr8:131024671..131030870,8	K562	blood:
26	chr8:131013499..131015985-chr8:131028051..131030878,2	MCF-7	breast:
27	chr8:131025540..131027750-chr8:131037896..131040382,2	MCF-7	breast:
28	chr8:131018416..131020834-chr8:131027208..131028989,2	MCF-7	breast:
29	chr8:131010470..131015100-chr8:131019285..131023448,5	K562	blood:
30	chr8:131006585..131008313-chr8:131019363..131020989,2	MCF-7	breast:
31	chr8:131007021..131009238-chr8:131011453..131013766,3	MCF-7	breast:
32	chr8:130950627..130952678-chr8:131014268..131017998,3	K562	blood:
33	chr8:131021262..131023800-chr8:131023935..131026265,2	MCF-7	breast:
34	chr8:130951528..130952250-chr8:131028470..131029127,2	MCF-7	breast:
35	chr8:131017010..131019589-chr8:131030192..131032616,2	K562	blood:
36	chr8:131011363..131013823-chr8:131017566..131020563,3	MCF-7	breast:
37	chr8:131027601..131029228-chr8:131030030..131032966,2	MCF-7	breast:
38	chr8:130950488..130952013-chr8:131029373..131031137,2	K562	blood:
39	chr8:131021262..131023800-chr8:131023935..131026265,2	MCF-7	breast:
40	chr8:131031108..131033473-chr8:131036840..131039215,2	MCF-7	breast:
41	chr8:130982299..130983095-chr8:131026665..131027754,4	MCF-7	breast:
42	chr8:131019270..131022496-chr8:131027575..131029857,4	MCF-7	breast:
43	chr8:130950508..130954142-chr8:131027064..131029855,6	MCF-7	breast:
44	chr8:130949866..130952104-chr8:131031388..131034166,2	K562	blood:
45	chr8:131006962..131012860-chr8:131027231..131029958,8	MCF-7	breast:
46	chr20:47442643..47444706-chr8:131026917..131028434,2	MCF-7	breast:
47	chr8:130949943..130953390-chr8:131026093..131029581,5	K562	blood:
48	chr8:131017010..131019589-chr8:131030192..131032616,2	K562	blood:
49	chr8:130908607..130911071-chr8:131026510..131028615,2	MCF-7	breast:
50	chr8:130981588..130985969-chr8:131027661..131030801,4	K562	blood:

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

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

miRNA name	Chromosome Location	mirBase accession
hsa-miR-5194	chr8:131020606-131020627	MIMAT0021125

No data

Variant related genes	Relation type
MIR5194	TF binding region
FAM49B	TF binding region
RNU7-181P	TF binding region
MIR5194	CpG island
FAM49B	CpG island
RNU7-181P	CpG island
ENSG00000253043	chromatin interactions
ENSG00000253720	chromatin interactions
ENSG00000153310	chromatin interactions
ENSG00000124126	chromatin interactions
ENSG00000264653	chromatin interactions

Extended variants
information (count: 1024 )
Associated
traits (count: 157 )

Variant overlapped rSNPs/rCNVs (count:1024 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6470788	chr8:131005345-131005346	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs548621581	chr8:131005403-131005404	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs567541684	chr8:131005412-131005413	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs183718126	chr8:131005415-131005416	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs553165178	chr8:131005423-131005424	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs571348623	chr8:131005435-131005436	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs188195818	chr8:131005439-131005440	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs192085892	chr8:131005449-131005450	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs199624843	chr8:131005481-131005482	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs370736413	chr8:131005510-131005511	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs184849431	chr8:131005588-131005589	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs575310859	chr8:131005664-131005665	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs541168946	chr8:131005746-131005747	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs189263864	chr8:131005762-131005763	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs577622007	chr8:131005774-131005775	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs573159932	chr8:131005779-131005780	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs191395150	chr8:131005795-131005796	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs545038622	chr8:131005814-131005815	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs565284700	chr8:131005875-131005876	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs139469219	chr8:131005876-131005877	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs544825564	chr8:131005878-131005879	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs562810114	chr8:131005909-131005910	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs530236687	chr8:131005965-131005966	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs144881761	chr8:131005969-131005970	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs566883439	chr8:131006001-131006002	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs147975671	chr8:131006062-131006063	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs576019643	chr8:131006108-131006109	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs533517906	chr8:131006119-131006120	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs75980645	chr8:131006179-131006180	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs184166453	chr8:131006187-131006188	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs189880547	chr8:131006239-131006240	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs117446365	chr8:131006258-131006259	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs181091038	chr8:131006303-131006304	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs368512881	chr8:131006318-131006319	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs572503010	chr8:131006323-131006324	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs550232483	chr8:131006324-131006325	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs186530239	chr8:131006400-131006401	Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs189222102	chr8:131006411-131006412	Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs181543029	chr8:131006412-131006413	Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs146607115	chr8:131006418-131006419	Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs186517548	chr8:131006442-131006443	Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs561750578	chr8:131006459-131006460	Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs190910384	chr8:131006460-131006461	Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs573977895	chr8:131006515-131006516	Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs56090609	chr8:131006516-131006517	Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs559517027	chr8:131006517-131006518	Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs112374684	chr8:131006518-131006519	Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs199794114	chr8:131006520-131006521	Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs397934244	chr8:131006523-131006524	Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs150465642	chr8:131006547-131006548	Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:157)

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
Breast cancer	16620391	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21611746	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Cancer	20164919	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1533 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:130996600-131009600	Weak transcription	Duodenum Smooth Muscle	Duodenum
2	chr8:130996600-131017400	Weak transcription	Fetal Intestine Small	intestine
3	chr8:130996800-131011600	Weak transcription	Left Ventricle	heart
4	chr8:130997000-131006800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr8:130997000-131006800	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr8:130997000-131006800	Weak transcription	Right Atrium	heart
7	chr8:130997000-131007000	Weak transcription	HSMMtube	muscle
8	chr8:130997000-131007600	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr8:130997000-131008600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr8:130997000-131008600	Weak transcription	Osteobl	bone
11	chr8:130997000-131009800	Weak transcription	Fetal Heart	heart
12	chr8:130997600-131007200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr8:130998400-131006600	Weak transcription	Esophagus	oesophagus
14	chr8:130998400-131006800	Weak transcription	Small Intestine	intestine
15	chr8:130998400-131007000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr8:130998400-131007400	Weak transcription	Fetal Muscle Leg	muscle
17	chr8:130998400-131008000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr8:130998400-131009000	Weak transcription	HUES64 Cell Line	embryonic stem cell
19	chr8:130998400-131017400	Weak transcription	Fetal Intestine Large	intestine
20	chr8:130998600-131007000	Weak transcription	Hela-S3	cervix
21	chr8:130998600-131009000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr8:130998600-131009600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr8:130998800-131006400	Weak transcription	Primary hematopoietic stem cells	blood
24	chr8:130999000-131006600	Weak transcription	Brain Angular Gyrus	brain
25	chr8:130999200-131006400	Weak transcription	Gastric	stomach
26	chr8:130999200-131007000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr8:130999400-131006800	Weak transcription	Pancreas	Pancrea
28	chr8:130999400-131008200	Weak transcription	Rectal Mucosa Donor 29	rectum
29	chr8:130999600-131006200	Weak transcription	Adipose Nuclei	Adipose
30	chr8:130999600-131006200	Weak transcription	HMEC	breast
31	chr8:130999600-131007000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
32	chr8:130999600-131008000	Weak transcription	Rectal Mucosa Donor 31	rectum
33	chr8:131000200-131006200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr8:131000400-131006800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr8:131000400-131008400	Weak transcription	Fetal Stomach	stomach
36	chr8:131000600-131006400	Weak transcription	Fetal Thymus	thymus
37	chr8:131000800-131006400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr8:131000800-131006800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr8:131001200-131008600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
40	chr8:131001400-131006200	Weak transcription	Brain Hippocampus Middle	brain
41	chr8:131001400-131006600	Weak transcription	Duodenum Mucosa	Duodenum
42	chr8:131001400-131008600	Weak transcription	H9 Cell Line	embryonic stem cell
43	chr8:131001600-131006200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
44	chr8:131001600-131006600	Weak transcription	Brain Cingulate Gyrus	brain
45	chr8:131001600-131009800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
46	chr8:131001800-131005800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
47	chr8:131001800-131006200	Weak transcription	Primary T helper cells PMA-I stimulated	--
48	chr8:131001800-131006200	Weak transcription	Brain Substantia Nigra	brain
49	chr8:131001800-131007400	Weak transcription	Sigmoid Colon	Sigmoid Colon
50	chr8:131001800-131009400	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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