Variant report

Variant	nsv533420
Chromosome Location	chr8:35358115-36227536
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2417)
CpG islands
(count:1952)
Chromatin interactive
region (count:48)
LncRNA
region (count:26)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2417 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:35998781-35999050	K562	blood:	n/a	n/a
2	ARID3A	chr8:35998754-35999027	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:35483342-35483547	HepG2	liver:	n/a	chr8:35483503-35483519 chr8:35483504-35483520
4	ATF1	chr8:35694479-35694576	K562	blood:	n/a	n/a
5	ATF1	chr8:35359837-35359860	K562	blood:	n/a	n/a
6	ATF1	chr8:35535442-35535506	K562	blood:	n/a	n/a
7	ATF2	chr8:35449571-35450010	GM12878	blood:	n/a	n/a
8	ATF2	chr8:35402765-35403153	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr8:35449456-35450056	GM12878	blood:	n/a	n/a
10	ATF2	chr8:35718359-35718833	GM12878	blood:	n/a	n/a
11	ATF2	chr8:35718465-35718780	GM12878	blood:	n/a	n/a
12	ATF2	chr8:35402728-35403206	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr8:35402916-35403184	H1-hESC	embryonic stem cell:	n/a	chr8:35402948-35402962
14	BACH1	chr8:36139227-36139586	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr8:35801904-35802359	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr8:35817981-35818072	K562	blood:	n/a	n/a
17	BACH1	chr8:36126038-36126313	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr8:35480385-35480401	K562	blood:	n/a	n/a
19	BACH1	chr8:35424139-35424252	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr8:35524193-35524227	K562	blood:	n/a	n/a
21	BACH1	chr8:35874478-35874818	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr8:35973723-35973757	K562	blood:	n/a	n/a
23	BACH1	chr8:36139222-36139571	K562	blood:	n/a	n/a
24	BATF	chr8:35767333-35767578	GM12878	blood:	n/a	n/a
25	BATF	chr8:35718466-35718742	GM12878	blood:	n/a	chr8:35718642-35718652
26	BATF	chr8:35718379-35718751	GM12878	blood:	n/a	chr8:35718642-35718652
27	BATF	chr8:35952817-35953061	GM12878	blood:	n/a	chr8:35952957-35952968
28	BCL11A	chr8:35718409-35718777	GM12878	blood:	n/a	n/a
29	BCL11A	chr8:35718438-35718749	GM12878	blood:	n/a	n/a
30	BCL11A	chr8:35755403-35755668	GM12878	blood:	n/a	n/a
31	BHLHE40	chr8:36127900-36128094	HepG2	liver:	n/a	n/a
32	BHLHE40	chr8:35768471-35768657	GM12878	blood:	n/a	n/a
33	BHLHE40	chr8:35755372-35755653	GM12878	blood:	n/a	n/a
34	BRCA1	chr8:35916503-35916505	GM12878	blood:	n/a	n/a
35	BRCA1	chr8:35725959-35725973	GM12878	blood:	n/a	n/a
36	CBX3	chr8:35817194-35817452	K562	blood:	n/a	n/a
37	CCNT2	chr8:35527398-35527598	K562	blood:	n/a	n/a
38	CEBPB	chr8:35555536-35555860	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr8:35637870-35638208	A549	lung:	n/a	chr8:35638032-35638041 chr8:35638031-35638042
40	CEBPB	chr8:35802637-35802717	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr8:35587784-35588055	K562	blood:	n/a	chr8:35587949-35587960 chr8:35587950-35587959 chr8:35587948-35587961 chr8:35587948-35587959
42	CEBPB	chr8:35367904-35368119	A549	lung:	n/a	n/a
43	CEBPB	chr8:36081963-36082234	HepG2	liver:	n/a	chr8:36082096-36082107
44	CEBPB	chr8:35575000-35575611	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr8:36202344-36202662	H1-hESC	embryonic stem cell:	n/a	chr8:36202485-36202494 chr8:36202483-36202496 chr8:36202484-36202495 chr8:36202483-36202494 chr8:36202485-36202494 chr8:36202485-36202494 chr8:36202485-36202494
46	CEBPB	chr8:35914872-35915081	HepG2	liver:	n/a	chr8:35914963-35914974 chr8:35914965-35914976 chr8:35914965-35914974
47	CEBPB	chr8:35643318-35643686	HepG2	liver:	n/a	chr8:35643499-35643510
48	CEBPB	chr8:36199377-36199577	K562	blood:	n/a	chr8:36199406-36199419 chr8:36199406-36199419
49	CEBPB	chr8:36005039-36005743	A549	lung:	n/a	chr8:36005181-36005192
50	CEBPB	chr8:35998793-35999054	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1952 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:35979338-35979388	NH-A	brain:	n/a
2	chr8:35391321-35391371	HRPEpiC	eye:	n/a
3	chr8:35576222-35576272	HCPEpiC	choroid plexus:	n/a
4	chr8:35649016-35649066	SK-N-SH	brain:	n/a
5	chr8:35440771-35440821	AG10803	skin:	n/a
6	chr8:35979108-35979158	GM12892	blood:	n/a
7	chr8:35762637-35762687	HEK293	kidney:	embryo
8	chr8:35576222-35576272	HL-60	blood:	n/a
9	chr8:35580715-35580765	HEEpiC	esophagus:	n/a
10	chr8:35979108-35979158	SK-N-MC	brain:	n/a
11	chr8:35580432-35580482	HCM	heart:	n/a
12	chr8:35452334-35452384	PANC-1	pancreas:	n/a
13	chr8:35979325-35979375	HRCEpiC	kidney:	n/a
14	chr8:35392042-35392092	H1-hESC	embryonic stem cell:	embryo
15	chr8:35452334-35452384	AG09319	gingival:	n/a
16	chr8:35803167-35803217	HepG2	liver:	n/a
17	chr8:35731494-35731544	SK-N-SH_RA	brain:	n/a
18	chr8:35762637-35762687	NHBE	bronchial:	n/a
19	chr8:35391321-35391371	AoSMC	blood vessel:	n/a
20	chr8:35581526-35581576	SKMC	muscle:	n/a
21	chr8:35580715-35580765	K562	blood:	n/a
22	chr8:35576222-35576272	HUVEC	blood vessel:	n/a
23	chr8:35580715-35580765	HRCEpiC	kidney:	n/a
24	chr8:35580715-35580765	SK-N-SH	brain:	n/a
25	chr8:35401908-35401958	HEEpiC	esophagus:	n/a
26	chr8:35979325-35979375	Jurkat	blood:	n/a
27	chr8:35979033-35979083	PrEC	prostate:	n/a
28	chr8:35440771-35440821	SK-N-SH_RA	brain:	n/a
29	chr8:35979338-35979388	NHBE	bronchial:	n/a
30	chr8:35580715-35580765	GM06990	blood:	n/a
31	chr8:35401313-35401363	ovcar-3	ovarian:	n/a
32	chr8:35979179-35979229	HCF	heart:	n/a
33	chr8:35401742-35401792	SK-N-MC	brain:	n/a
34	chr8:35803167-35803217	ovcar-3	ovarian:	n/a
35	chr8:35401742-35401792	RPTEC	kidney:	n/a
36	chr8:35580432-35580482	BE2_C	brain:	n/a
37	chr8:35685207-35685257	GM06990	blood:	n/a
38	chr8:35979108-35979158	HUVEC	blood vessel:	n/a
39	chr8:35685207-35685257	Hepatocyte	liver:	n/a
40	chr8:35581526-35581576	GM12891	blood:	n/a
41	chr8:35392042-35392092	ProgFib	skin:	n/a
42	chr8:35440771-35440821	MCF-7	breast:	n/a
43	chr8:35452334-35452384	AoSMC	blood vessel:	n/a
44	chr8:35744638-35744688	HRPEpiC	eye:	n/a
45	chr8:35576222-35576272	CMK	blood:	n/a
46	chr8:35580715-35580765	AG04450	lung:	fetal
47	chr8:35401670-35401720	PrEC	prostate:	n/a
48	chr8:35649016-35649066	PrEC	prostate:	n/a
49	chr8:35979179-35979229	Hepatocyte	liver:	n/a
50	chr8:35540239-35540289	MCF-7	breast:	n/a

(count:48 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:36214537..36217375-chr8:36218045..36219768,2	K562	blood:
2	chr7:98429076..98431489-chr8:36223053..36226052,2	MCF-7	breast:
3	chr8:35596968..35598886-chr8:35604620..35606278,2	K562	blood:
4	chr17:41401117..41402640-chr8:35678068..35679569,2	K562	blood:
5	chr17:41464397..41466335-chr8:35678069..35679588,3	K562	blood:
6	chr8:36184128..36185820-chr8:36198877..36200625,2	K562	blood:
7	chr8:35018612..35019300-chr8:35998668..35999178,2	MCF-7	breast:
8	chr8:35296451..35297364-chr8:35998554..35999313,2	MCF-7	breast:
9	chr8:35899435..35901974-chr8:35902766..35905726,2	K562	blood:
10	chr8:35899435..35901974-chr8:35902766..35905726,2	K562	blood:
11	chr8:35787657..35788212-chr8:35806131..35807030,2	MCF-7	breast:
12	chr17:41463858..41466219-chr8:35678069..35679569,3	K562	blood:
13	chr8:35638386..35640452-chr8:35642289..35644463,2	K562	blood:
14	chr8:35431521..35433590-chr8:35435377..35437047,2	K562	blood:
15	chr8:35998628..35999297-chr8:36630776..36631627,3	MCF-7	breast:
16	chr8:35744346..35744912-chr8:35998590..35999359,2	MCF-7	breast:
17	chr8:35497530..35499054-chr8:35564853..35566842,2	K562	blood:
18	chr8:36173773..36176086-chr8:36196865..36199430,2	MCF-7	breast:
19	chr8:35787657..35788212-chr8:35806131..35807030,2	MCF-7	breast:
20	chr8:35638386..35640452-chr8:35642289..35644463,2	K562	blood:
21	chr8:35452680..35453282-chr8:35998615..35999410,2	MCF-7	breast:
22	chr8:35009843..35010391-chr8:35998408..35998917,2	MCF-7	breast:
23	chr17:41398363..41402584-chr8:35679569..35681089,3	K562	blood:
24	chr8:35009829..35010450-chr8:35998446..35999665,3	MCF-7	breast:
25	chr8:36214348..36217156-chr8:36228449..36231444,2	MCF-7	breast:
26	chr8:36173773..36176086-chr8:36196865..36199430,2	MCF-7	breast:
27	chr8:35431521..35433590-chr8:35435377..35437047,2	K562	blood:
28	chr17:41399296..41402359-chr8:35678068..35681088,3	MCF-7	breast:
29	chr8:36214537..36217375-chr8:36218045..36219768,2	K562	blood:
30	chr17:41380631..41382205-chr8:35678068..35679588,2	MCF-7	breast:
31	chr3:73158515..73160568-chr8:35679569..35681069,2	K562	blood:
32	chr8:35452680..35453282-chr8:35998615..35999410,2	MCF-7	breast:
33	chr8:36036347..36039298-chr8:36039472..36041633,2	MCF-7	breast:
34	chr8:35993182..35994756-chr8:35996509..35999089,2	K562	blood:
35	chr8:33663430..33663957-chr8:35744542..35745198,2	MCF-7	breast:
36	chr3:73159093..73162068-chr8:35678068..35679569,2	MCF-7	breast:
37	chr8:35744346..35744912-chr8:35998590..35999359,2	MCF-7	breast:
38	chr8:36215520..36217788-chr8:36221980..36223861,2	K562	blood:
39	chr8:36184128..36185820-chr8:36198877..36200625,2	K562	blood:
40	chr8:35596968..35598886-chr8:35604620..35606278,2	K562	blood:
41	chr8:35620195..35622822-chr8:35626883..35629554,2	K562	blood:
42	chr8:36036347..36039298-chr8:36039472..36041633,2	MCF-7	breast:
43	chr13:35589705..35590705-chr8:36059332..36059852,2	MCF-7	breast:
44	chr17:41400768..41402617-chr8:35678068..35679569,3	K562	blood:
45	chr8:35497530..35499054-chr8:35564853..35566842,2	K562	blood:
46	chr8:35993182..35994756-chr8:35996509..35999089,2	K562	blood:
47	chr8:36215520..36217788-chr8:36221980..36223861,2	K562	blood:
48	chr8:35620195..35622822-chr8:35626883..35629554,2	K562	blood:

(count:26 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-419C23.1.1-4	chr8:35861834-35862110	ENSG00000253524
2	lnc-UNC5D-2	chr8:35750072-35750201	ENSG00000253452
3	lnc-UNC5D-2	chr8:35757901-35758022	ENSG00000253452
4	lnc-UNC5D-2	chr8:35788183-35788228	ENSG00000253452
5	lnc-RP11-419C23.1.1-11	chr8:36083091-36083154	NONHSAT126011
6	lnc-UNC5D-5	chr8:36124003-36124282	NONHSAT126012
7	lnc-UNC5D-2	chr8:35720025-35720138	ENSG00000253452
8	lnc-UNC5D-2	chr8:35783552-35783638	ENSG00000253452
9	lnc-UNC5D-2	chr8:35719641-35719668	ENSG00000253452
10	lnc-RP11-419C23.1.1-8	chr8:36178665-36178922	NONHSAT126017
11	lnc-UNC5D-2	chr8:35757901-35758022	ENSG00000253452
12	lnc-UNC5D-2	chr8:35828131-35828183	ENSG00000253452
13	lnc-RP11-419C23.1.1-9	chr8:36137009-36137214	NONHSAT126015
14	lnc-UNC5D-2	chr8:35750072-35750201	ENSG00000253452
15	lnc-RP11-419C23.1.1-8	chr8:36178557-36178598	NONHSAT126017
16	lnc-RP11-419C23.1.1-4	chr8:35951496-35951527	ENSG00000253524
17	lnc-RP11-419C23.1.1-4	chr8:35892385-35892466	ENSG00000253524
18	lnc-RP11-419C23.1.1-4	chr8:35951496-35951543	ENSG00000253524
19	lnc-UNC5D-6	chr8:36136478-36137001	NONHSAT126014
20	lnc-RP11-419C23.1.1-4	chr8:35861838-35862110	ENSG00000253524
21	lnc-UNC5D-2	chr8:35801762-35801920	ENSG00000253452
22	lnc-RP11-419C23.1.1-12	chr8:35978916-35979201	NONHSAT126010
23	lnc-UNC5D-2	chr8:35720027-35720138	ENSG00000253452
24	lnc-RP11-419C23.1.1-11	chr8:36088465-36088673	NONHSAT126011
25	lnc-UNC5D-2	chr8:35787238-35787275	ENSG00000253452
26	lnc-RP11-419C23.1.1-4	chr8:35952530-35952564	ENSG00000253524

No data

Variant related genes	Relation type
UNC5D	TF binding region
RNU6-533P	TF binding region
ENSG00000254309	TF binding region
ENSG00000253504	TF binding region
ENSG00000253685	TF binding region
MTND6P19	TF binding region
ENSG00000253610	TF binding region
ENSG00000254320	TF binding region
ENSG00000253452	TF binding region
ENSG00000253524	TF binding region
LSM12P1	TF binding region
RN7SKP201	TF binding region
ENSG00000233863	TF binding region
UNC5D	CpG island
RNU6-533P	CpG island
ENSG00000254309	CpG island
ENSG00000253504	CpG island
ENSG00000253685	CpG island
MTND6P19	CpG island
ENSG00000253610	CpG island
ENSG00000254320	CpG island
ENSG00000253452	CpG island
ENSG00000253524	CpG island
LSM12P1	CpG island
RN7SKP201	CpG island
ENSG00000233863	CpG island
ENSG00000188825	chromatin interactions
ENSG00000223247	chromatin interactions
ENSG00000236383	chromatin interactions

Extended variants
information (count: 19475 )
Associated
traits (count: 126 )

Variant overlapped rSNPs/rCNVs (count:19475 , 50 per page) page: 1 2 3 4 5 6 7 ... 390

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs113633482	chr8:35358152-35358153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs372012849	chr8:35358157-35358158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs559227675	chr8:35358199-35358200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs577461365	chr8:35358200-35358201	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs375902784	chr8:35358230-35358231	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs541648363	chr8:35358261-35358262	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs112385815	chr8:35358283-35358284	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs142711126	chr8:35358294-35358295	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs574644008	chr8:35358295-35358296	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs192625788	chr8:35358432-35358433	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs150507590	chr8:35358433-35358434	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs568765565	chr8:35358438-35358439	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs34532946	chr8:35358464-35358465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs573184249	chr8:35358465-35358466	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs370305800	chr8:35358468-35358469	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs530968549	chr8:35358572-35358573	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs552285791	chr8:35358606-35358607	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs184499100	chr8:35358618-35358619	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs117827874	chr8:35358622-35358623	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs139482136	chr8:35358683-35358684	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs149687678	chr8:35358696-35358697	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs568080072	chr8:35358713-35358714	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs548342241	chr8:35358763-35358764	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs569632055	chr8:35358786-35358787	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs116004893	chr8:35358799-35358800	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs189268659	chr8:35358816-35358817	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs535419507	chr8:35358855-35358856	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs76180405	chr8:35358869-35358870	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs565744609	chr8:35358873-35358874	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs534400757	chr8:35358913-35358914	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs553221531	chr8:35359003-35359004	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs145525695	chr8:35359018-35359019	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs542002509	chr8:35359069-35359070	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs557060629	chr8:35359103-35359104	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs575641265	chr8:35359138-35359139	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs546238732	chr8:35359228-35359229	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs372816775	chr8:35359254-35359255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs181962953	chr8:35359369-35359370	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs369829070	chr8:35359418-35359419	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs373247461	chr8:35359419-35359420	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs528460425	chr8:35359531-35359532	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs574147372	chr8:35359554-35359555	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs541354863	chr8:35359557-35359558	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs559672336	chr8:35359600-35359601	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs76836997	chr8:35359601-35359602	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs541203561	chr8:35359603-35359604	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs184593533	chr8:35359614-35359615	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs569769762	chr8:35359670-35359671	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs140881997	chr8:35359673-35359674	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs189914447	chr8:35359752-35359753	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:126)

Disease	PMID	Source
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	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
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Prostate cancer	21965145	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
Colorectal cancer	16272173	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
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
Seminomas	18059402	CNVD
Lung cancer	18438408	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
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Multiple myeloma	16616336	CNVD
Melanoma	20688739	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	21806811	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hepatocellular carcinoma	16750200	CNVD
Bladder cancer	19088036	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	20459607	CNVD
Renal cell carcinoma	18765545	CNVD
Colorectal cancer	16912164	CNVD
Neuroticism	17667963	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	17001308	CNVD
Breast cancer	17157792	CNVD
Cancer	17001308	CNVD
Cancer	18840272	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	18382360	CNVD
Ductal carcinoma	18381933	CNVD
Breast cancer	21328542	CNVD
Squamous cell cancer	20885788	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Intellectual disability	22045946	CNVD
Lung cancer	17925434	CNVD
Uveal melanoma	20484589	CNVD
Breast cancer	16608533	CNVD
Breast cancer	21364760	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Renal cell carcinoma	21215367	CNVD
Chordoma	21215367	CNVD
Acute myeloid leukemia	19651600	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:2244 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:35356400-35391200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr8:35356800-35358400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr8:35356800-35358800	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr8:35357000-35358200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr8:35357000-35358200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr8:35357000-35358400	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr8:35357000-35358400	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr8:35357600-35358200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr8:35358200-35359200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr8:35358200-35359600	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr8:35358200-35359800	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr8:35358400-35359200	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr8:35358400-35359800	Enhancers	H1 Cell Line	embryonic stem cell
14	chr8:35358400-35359800	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr8:35358800-35359600	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr8:35359200-35359600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr8:35359200-35371600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr8:35359600-35359800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr8:35359800-35361600	Weak transcription	HUES48 Cell Line	embryonic stem cell
20	chr8:35359800-35361600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr8:35359800-35397200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr8:35361600-35362000	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr8:35361600-35362000	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr8:35361600-35362200	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr8:35361600-35366000	Weak transcription	Fetal Brain Female	brain
26	chr8:35361800-35362000	Enhancers	H1 Cell Line	embryonic stem cell
27	chr8:35361800-35362400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr8:35361800-35362600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr8:35361800-35362600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr8:35362400-35368000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr8:35362600-35363000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr8:35362600-35364000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr8:35363000-35363200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr8:35363000-35363600	Enhancers	Fetal Lung	lung
35	chr8:35363200-35365600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr8:35364000-35364200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr8:35365400-35366800	Enhancers	Cortex derived primary cultured neurospheres	brain
38	chr8:35365600-35366200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr8:35365600-35366400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr8:35366000-35366200	Enhancers	Fetal Brain Male	brain
41	chr8:35366000-35366400	Enhancers	Fetal Brain Female	brain
42	chr8:35366000-35366800	Enhancers	Fetal Heart	heart
43	chr8:35366000-35366800	Enhancers	Fetal Muscle Leg	muscle
44	chr8:35366200-35366800	Weak transcription	Fetal Brain Male	brain
45	chr8:35366400-35368000	Weak transcription	Fetal Brain Female	brain
46	chr8:35366800-35367000	Enhancers	Fetal Brain Male	brain
47	chr8:35366800-35371600	Weak transcription	Cortex derived primary cultured neurospheres	brain
48	chr8:35366800-35371600	Weak transcription	Fetal Muscle Leg	muscle
49	chr8:35367000-35371200	Weak transcription	Fetal Brain Male	brain
50	chr8:35368000-35368200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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