Variant report

Variant	esv2759452
Chromosome Location	chr6:87456503-87645214
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:87535126-87535556	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:87566680-87567004	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:87566708-87567012	K562	blood:	n/a	n/a
4	BCL11A	chr6:87466373-87466627	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr6:87530476-87530779	GM12878	blood:	n/a	n/a
6	CBX3	chr6:87469730-87470014	K562	blood:	n/a	n/a
7	CCNT2	chr6:87462269-87462510	K562	blood:	n/a	n/a
8	CEBPB	chr6:87487584-87487974	MCF-7	breast:	n/a	chr6:87487835-87487846
9	CEBPB	chr6:87456318-87456518	H1-hESC	embryonic stem cell:	n/a	chr6:87456436-87456447
10	CEBPB	chr6:87487691-87487983	K562	blood:	n/a	chr6:87487835-87487846
11	CEBPB	chr6:87582556-87582895	MCF-7	breast:	n/a	chr6:87582731-87582742
12	CEBPB	chr6:87487669-87488013	HepG2	liver:	n/a	chr6:87487835-87487846
13	CEBPB	chr6:87487799-87487907	H1-hESC	embryonic stem cell:	n/a	chr6:87487835-87487846
14	CEBPB	chr6:87487730-87487984	A549	lung:	n/a	chr6:87487835-87487846
15	CEBPB	chr6:87487594-87488059	MCF-7	breast:	n/a	chr6:87487835-87487846
16	CEBPB	chr6:87582634-87582782	HepG2	liver:	n/a	chr6:87582731-87582742
17	CEBPB	chr6:87566699-87567040	MCF-7	breast:	n/a	chr6:87566793-87566806
18	CEBPB	chr6:87487702-87487991	IMR90	lung:	n/a	chr6:87487835-87487846
19	CEBPB	chr6:87456275-87456563	HepG2	liver:	n/a	chr6:87456436-87456447
20	CEBPB	chr6:87566545-87566969	MCF-7	breast:	n/a	chr6:87566793-87566806
21	CEBPB	chr6:87582620-87582898	HepG2	liver:	n/a	chr6:87582731-87582742
22	CEBPB	chr6:87486237-87486275	A549	lung:	n/a	chr6:87486256-87486269
23	CREB1	chr6:87466320-87466767	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr6:87601780-87601930	GM12873	blood:	n/a	n/a
25	CTCF	chr6:87566800-87566950	BJ	skin:	n/a	chr6:87566859-87566875 chr6:87566864-87566873 chr6:87566860-87566873 chr6:87566858-87566876 chr6:87566853-87566874
26	CTCF	chr6:87601720-87601870	HEK293	kidney:	n/a	n/a
27	CTCF	chr6:87569360-87569510	HepG2	liver:	n/a	n/a
28	CTCF	chr6:87566780-87566930	Caco-2	colon:	n/a	chr6:87566859-87566875 chr6:87566864-87566873 chr6:87566860-87566873 chr6:87566858-87566876 chr6:87566853-87566874
29	CTCF	chr6:87566800-87566950	K562	blood:	n/a	chr6:87566859-87566875 chr6:87566864-87566873 chr6:87566860-87566873 chr6:87566858-87566876 chr6:87566853-87566874
30	CTCF	chr6:87566800-87566950	HAc	cerebellar:	n/a	chr6:87566859-87566875 chr6:87566864-87566873 chr6:87566860-87566873 chr6:87566858-87566876 chr6:87566853-87566874
31	CTCF	chr6:87566800-87566950	HPAF	blood vessel:	n/a	chr6:87566859-87566875 chr6:87566864-87566873 chr6:87566860-87566873 chr6:87566858-87566876 chr6:87566853-87566874
32	CTCF	chr6:87569320-87569470	NHEK	skin:	n/a	n/a
33	CTCF	chr6:87566860-87567010	HCM	heart:	n/a	chr6:87566864-87566873 chr6:87566860-87566873
34	CTCF	chr6:87569400-87569550	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr6:87601740-87601890	GM06990	blood:	n/a	n/a
36	CTCF	chr6:87566752-87566990	Pancreas_OC	pancreas:	n/a	chr6:87566859-87566875 chr6:87566864-87566873 chr6:87566860-87566873 chr6:87566858-87566876 chr6:87566853-87566874
37	CTCF	chr6:87566606-87567158	MCF-7	breast:	n/a	chr6:87566859-87566875 chr6:87566864-87566873 chr6:87566860-87566873 chr6:87566858-87566876 chr6:87566853-87566874
38	CTCF	chr6:87522206-87522233	GM10266	blood:	n/a	n/a
39	CTCF	chr6:87569380-87569530	GM12873	blood:	n/a	n/a
40	CTCF	chr6:87488757-87488820	MCF-7	breast:	n/a	n/a
41	CTCF	chr6:87566820-87566970	HPF	lung:	n/a	chr6:87566859-87566875 chr6:87566864-87566873 chr6:87566860-87566873 chr6:87566858-87566876 chr6:87566853-87566874
42	CTCF	chr6:87601700-87601850	NB4	blood:	n/a	n/a
43	CTCF	chr6:87566770-87566974	Kidney_OC	kidney:	n/a	chr6:87566859-87566875 chr6:87566864-87566873 chr6:87566860-87566873 chr6:87566858-87566876 chr6:87566853-87566874
44	CTCF	chr6:87601735-87601799	MCF-7	breast:	n/a	n/a
45	CTCF	chr6:87566750-87566990	GM10266	blood:	n/a	chr6:87566859-87566875 chr6:87566864-87566873 chr6:87566860-87566873 chr6:87566858-87566876 chr6:87566853-87566874
46	CTCF	chr6:87601660-87601810	HepG2	liver:	n/a	n/a
47	CTCF	chr6:87566920-87567070	A549	lung:	n/a	n/a
48	CTCF	chr6:87566750-87566959	GM13976	blood:	n/a	chr6:87566859-87566875 chr6:87566864-87566873 chr6:87566860-87566873 chr6:87566858-87566876 chr6:87566853-87566874
49	CTCF	chr6:87566780-87566930	GM06990	blood:	n/a	chr6:87566859-87566875 chr6:87566864-87566873 chr6:87566860-87566873 chr6:87566858-87566876 chr6:87566853-87566874
50	CTCF	chr6:87492180-87492330	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:87607655-87607705	HIPEpiC	eye:	n/a
2	chr6:87607195-87607245	HCT-116	colon:	n/a
3	chr6:87607744-87607794	PFSK-1	brain:	n/a
4	chr6:87643469-87643519	SK-N-SH_RA	brain:	n/a
5	chr6:87607161-87607211	HPAEpiC	pulmonary alveolar:	n/a
6	chr6:87466574-87466624	AoSMC	blood vessel:	n/a
7	chr6:87466574-87466624	HUVEC	blood vessel:	n/a
8	chr6:87607161-87607211	NHDF-neo	bronchial:	n/a
9	chr6:87643469-87643519	PANC-1	pancreas:	n/a
10	chr6:87643469-87643519	H1-hESC	embryonic stem cell:	embryo
11	chr6:87607655-87607705	MCF-7	breast:	n/a
12	chr6:87607195-87607245	AG04449	skin:	fetal
13	chr6:87607655-87607705	AoSMC	blood vessel:	n/a
14	chr6:87607178-87607228	ProgFib	skin:	n/a
15	chr6:87607195-87607245	HRCEpiC	kidney:	n/a
16	chr6:87643469-87643519	AG10803	skin:	n/a
17	chr6:87607195-87607245	AG09319	gingival:	n/a
18	chr6:87607655-87607705	ECC-1	luminal epithelium:	n/a
19	chr6:87607744-87607794	A549	lung:	n/a
20	chr6:87607744-87607794	GM19239	blood:	n/a
21	chr6:87643469-87643519	CMK	blood:	n/a
22	chr6:87607744-87607794	NH-A	brain:	n/a
23	chr6:87607744-87607794	AG09319	gingival:	n/a
24	chr6:87607655-87607705	SK-N-SH_RA	brain:	n/a
25	chr6:87607744-87607794	ovcar-3	ovarian:	n/a
26	chr6:87607178-87607228	HIPEpiC	eye:	n/a
27	chr6:87643469-87643519	HCPEpiC	choroid plexus:	n/a
28	chr6:87607744-87607794	SK-N-MC	brain:	n/a
29	chr6:87607178-87607228	HUVEC	blood vessel:	n/a
30	chr6:87466574-87466624	GM06990	blood:	n/a
31	chr6:87607195-87607245	HCF	heart:	n/a
32	chr6:87607178-87607228	SKMC	muscle:	n/a
33	chr6:87643469-87643519	HCF	heart:	n/a
34	chr6:87607195-87607245	GM12891	blood:	n/a
35	chr6:87466574-87466624	GM12878	blood:	n/a
36	chr6:87643469-87643519	AG09309	skin:	n/a
37	chr6:87643469-87643519	HepG2	liver:	n/a
38	chr6:87607655-87607705	BJ	skin:	n/a
39	chr6:87607744-87607794	PrEC	prostate:	n/a
40	chr6:87607655-87607705	SK-N-MC	brain:	n/a
41	chr6:87466574-87466624	HCPEpiC	choroid plexus:	n/a
42	chr6:87607744-87607794	GM12892	blood:	n/a
43	chr6:87607744-87607794	AG09309	skin:	n/a
44	chr6:87607744-87607794	Hepatocyte	liver:	n/a
45	chr6:87607161-87607211	ovcar-3	ovarian:	n/a
46	chr6:87607655-87607705	HCF	heart:	n/a
47	chr6:87643469-87643519	GM12878	blood:	n/a
48	chr6:87607178-87607228	Hepatocyte	liver:	n/a
49	chr6:87466574-87466624	AG04449	skin:	fetal
50	chr6:87643469-87643519	HRPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:87433212..87433993-chr6:87487281..87488109,4	MCF-7	breast:
2	chr6:87570969..87571590-chr6:87646510..87647169,2	MCF-7	breast:
3	chr6:87569023..87569900-chr6:87646597..87647139,2	MCF-7	breast:
4	chr6:87570712..87571662-chr6:87646445..87647351,6	MCF-7	breast:
5	chr6:87433571..87436009-chr6:87486240..87488175,2	MCF-7	breast:
6	chr6:87566606..87567119-chr6:87739226..87739851,2	MCF-7	breast:
7	chr17:59694281..59694801-chr6:87560393..87561118,2	MCF-7	breast:
8	chr6:87533978..87535623-chr6:87543693..87545877,2	K562	blood:
9	chr6:87494778..87497258-chr6:87499826..87502214,2	K562	blood:
10	chr6:87494778..87497258-chr6:87499826..87502214,2	K562	blood:
11	chr6:87624618..87626142-chr6:87628674..87631673,2	K562	blood:
12	chr6:87624618..87626142-chr6:87628674..87631673,2	K562	blood:
13	chr6:87565888..87566776-chr6:87646668..87647203,2	MCF-7	breast:
14	chr6:87432080..87434373-chr6:87487910..87490262,2	MCF-7	breast:
15	chr1:144533824..144534363-chr6:87480670..87481670,2	HCT-116	colon:
16	chr6:86463941..86466706-chr6:87565460..87567312,2	MCF-7	breast:
17	chr6:87491790..87492456-chr6:87566446..87567164,4	MCF-7	breast:
18	chr6:87569382..87569938-chr6:87739160..87740006,3	MCF-7	breast:
19	chr1:144532698..144535379-chr6:87481170..87482690,3	K562	blood:
20	chr6:87494199..87497258-chr6:87499220..87502214,3	K562	blood:
21	chr6:87533978..87535623-chr6:87543693..87545877,2	K562	blood:
22	chr6:87494199..87497258-chr6:87499220..87502214,3	K562	blood:
23	chr6:87491790..87492456-chr6:87566446..87567164,4	MCF-7	breast:
24	chr6:87569162..87570137-chr6:87646249..87647415,7	MCF-7	breast:
25	chr6:87569230..87570355-chr6:87738909..87740054,4	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CGA-5	chr6:87547915-87548191	NONHSAT113887
2	lnc-CGA-5	chr6:87641630-87641702	NONHSAT113887
3	lnc-CGA-5	chr6:87540309-87542399	NONHSAT113886
4	lnc-CGA-5	chr6:87638499-87638629	NONHSAT113887
5	lnc-CGA-5	chr6:87548088-87548191	NONHSAT113886
6	lnc-CGA-6	chr6:87478240-87478650	NONHSAT113884

Variant related genes	Relation type
ENSG00000217769	TF binding region
ENSG00000219190	TF binding region
HTR1E	TF binding region
ENSG00000220240	TF binding region
ENSG00000217769	CpG island
ENSG00000219190	CpG island
HTR1E	CpG island
ENSG00000220240	CpG island
ENSG00000168830	chromatin interactions
ENSG00000201699	chromatin interactions

Extended variants
information (count: 2468 )
Associated
traits (count: 112 )

Variant overlapped rSNPs/rCNVs (count:2468 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs540799255	chr6:87465232-87465233	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs535488575	chr6:87465257-87465258	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs550318295	chr6:87465261-87465262	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs568839340	chr6:87465324-87465325	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs183769157	chr6:87465343-87465344	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs188149167	chr6:87465348-87465349	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs73492070	chr6:87465363-87465364	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs534125806	chr6:87465429-87465430	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs573785529	chr6:87465490-87465491	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs147943567	chr6:87465519-87465520	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs80014355	chr6:87465531-87465532	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs181278562	chr6:87465533-87465534	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs17435044	chr6:87465560-87465561	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs148565018	chr6:87465621-87465622	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs564031156	chr6:87465692-87465693	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs111562561	chr6:87465730-87465731	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs520731	chr6:87465749-87465750	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs186437118	chr6:87465795-87465796	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs562129842	chr6:87465801-87465802	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs550625418	chr6:87465815-87465816	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs563923649	chr6:87465879-87465880	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs149549628	chr6:87465880-87465881	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs190040308	chr6:87465883-87465884	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs539428817	chr6:87465909-87465910	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs552148176	chr6:87465912-87465913	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs567171839	chr6:87465931-87465932	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs181670600	chr6:87465935-87465936	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs555696678	chr6:87465936-87465937	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs151071921	chr6:87465986-87465987	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs187191103	chr6:87465987-87465988	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs78858742	chr6:87466030-87466031	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs577657131	chr6:87466098-87466099	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs9362359	chr6:87466134-87466135	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs140979397	chr6:87466183-87466184	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs573065524	chr6:87466226-87466227	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs113630234	chr6:87466253-87466254	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs200814437	chr6:87466267-87466268	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs9353424	chr6:87466268-87466269	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs79759620	chr6:87466269-87466270	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs561758509	chr6:87466270-87466271	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs192119481	chr6:87466278-87466279	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs544013220	chr6:87466283-87466284	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs541546830	chr6:87466345-87466346	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs533008906	chr6:87466374-87466375	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs551404316	chr6:87466406-87466407	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs74555988	chr6:87466414-87466415	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs563953603	chr6:87466473-87466474	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs493187	chr6:87466492-87466493	Enhancers Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
49	rs567798141	chr6:87466535-87466536	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs145027249	chr6:87466579-87466580	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:112)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Autism	22495311	CNVD
Gastric cancer	17908304	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Systemic lupus erythematosus	17503323	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Follicular lymphoma	17699855	CNVD
Breast cancer	17133270	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Lung adenocarcinoma	21935476	CNVD
Prostate cancer	16461572	CNVD
Mental retardation	21045960	CNVD
Obesity	21045960	CNVD
learning difficulties	21045960	CNVD
Prostate cancer	17245344	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Cancer	20164920	CNVD
Burkitt''s lymphoma	20823134	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
craniofacial dysmorphism	21918468	CNVD
Myelofibrosis	22110671	CNVD
Neurodevelopmental disorder	22521361	CNVD
abnormal development	18461090	CNVD
Myelodysplastic syndrome	18508791	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	21364760	CNVD
Developmental delay	19490664	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Urothelial cell carcinoma	18451213	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:148 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:87465200-87465800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
2	chr6:87465200-87468200	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr6:87465400-87466200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr6:87465400-87467000	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr6:87465400-87468000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr6:87465400-87468000	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr6:87465600-87466200	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr6:87465800-87467000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr6:87465800-87467000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr6:87465800-87467200	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr6:87466000-87467000	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr6:87466000-87467200	Enhancers	H1 Cell Line	embryonic stem cell
13	chr6:87466200-87466400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
14	chr6:87466200-87466800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr6:87466400-87466800	Enhancers	H9 Cell Line	embryonic stem cell
16	chr6:87466400-87466800	Active TSS	iPS-20b Cell Line	embryonic stem cell
17	chr6:87466800-87467000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr6:87466800-87467000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
19	chr6:87466800-87467800	Weak transcription	H9 Cell Line	embryonic stem cell
20	chr6:87467000-87467200	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr6:87467000-87467400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr6:87467200-87467800	Weak transcription	H1 Cell Line	embryonic stem cell
23	chr6:87467400-87469200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr6:87467800-87468000	Enhancers	H1 Cell Line	embryonic stem cell
25	chr6:87467800-87468000	Enhancers	H9 Cell Line	embryonic stem cell
26	chr6:87469200-87470200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
27	chr6:87469200-87470800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr6:87482400-87482800	Enhancers	Fetal Intestine Large	intestine
29	chr6:87483200-87483800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr6:87484800-87485200	Enhancers	Esophagus	oesophagus
31	chr6:87493800-87494600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr6:87493800-87494800	Enhancers	Fetal Kidney	kidney
33	chr6:87494600-87494800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr6:87494600-87494800	Enhancers	Fetal Intestine Large	intestine
35	chr6:87494800-87495400	Weak transcription	Fetal Intestine Large	intestine
36	chr6:87494800-87495600	Weak transcription	Fetal Kidney	kidney
37	chr6:87494800-87495800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr6:87495400-87496200	Enhancers	Fetal Intestine Large	intestine
39	chr6:87495600-87495800	Enhancers	Fetal Kidney	kidney
40	chr6:87495800-87496400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr6:87496400-87496600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr6:87525400-87525600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr6:87525400-87525800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr6:87525600-87525800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr6:87528600-87529400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
46	chr6:87534600-87536000	Enhancers	Liver	Liver
47	chr6:87534600-87536400	Enhancers	HepG2	liver
48	chr6:87535800-87536000	Enhancers	Pancreatic Islets	Pancreatic Islet
49	chr6:87536200-87537600	Weak transcription	Pancreatic Islets	Pancreatic Islet
50	chr6:87536800-87537600	Enhancers	Fetal Intestine Large	intestine

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