Variant report

Variant	nsv5386
Chromosome Location	chr6:88038551-88044921
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:83)
CpG islands
(count:245)
Chromatin interactive
region (count:6)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:83 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr6:88043598-88043928	K562	blood:	n/a	n/a
2	BHLHE40	chr6:88042733-88043021	K562	blood:	n/a	n/a
3	CEBPB	chr6:88043397-88043709	IMR90	lung:	n/a	n/a
4	CEBPB	chr6:88043501-88043702	HepG2	liver:	n/a	n/a
5	CEBPB	chr6:88043390-88043722	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr6:88043399-88043713	K562	blood:	n/a	n/a
7	CEBPB	chr6:88038751-88038949	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr6:88039588-88039606	K562	blood:	n/a	n/a
9	CHD2	chr6:88038816-88038832	H1-hESC	embryonic stem cell:	n/a	n/a
10	CHD2	chr6:88038824-88038952	Hela-S3	cervix:	n/a	n/a
11	CTCF	chr6:88043020-88043170	GM12864	blood:	n/a	n/a
12	CTCF	chr6:88043160-88043310	GM12872	blood:	n/a	chr6:88043188-88043197
13	CTCF	chr6:88040540-88040690	HRE	kidney:	n/a	n/a
14	E2F6	chr6:88042623-88043051	H1-hESC	embryonic stem cell:	n/a	n/a
15	EGR1	chr6:88038553-88038763	K562	blood:	n/a	n/a
16	FOS	chr6:88043408-88043626	MCF10A-Er-Src	breast:	n/a	n/a
17	FOS	chr6:88043407-88043686	MCF10A-Er-Src	breast:	n/a	n/a
18	FOS	chr6:88043475-88043703	MCF10A-Er-Src	breast:	n/a	n/a
19	FOS	chr6:88043408-88043686	MCF10A-Er-Src	breast:	n/a	n/a
20	FOXA2	chr6:88038367-88038712	A549	lung:	n/a	n/a
21	FOXA2	chr6:88038204-88038811	A549	lung:	n/a	n/a
22	GTF2F1	chr6:88042673-88042693	H1-hESC	embryonic stem cell:	n/a	n/a
23	HA-E2F1	chr6:88038516-88038921	MCF-7	breast:	n/a	n/a
24	IRF1	chr6:88040262-88040273	K562	blood:	n/a	n/a
25	JUN	chr6:88041509-88041653	K562	blood:	n/a	n/a
26	KAP1	chr6:88043367-88043932	HEK293	kidney:	n/a	n/a
27	KAP1	chr6:88038534-88039171	HEK293	kidney:	n/a	n/a
28	KAP1	chr6:88043409-88043863	U2OS	brain:	n/a	n/a
29	MAX	chr6:88042454-88042465	A549	lung:	n/a	n/a
30	MAX	chr6:88042700-88043049	K562	blood:	n/a	chr6:88042879-88042889
31	MAX	chr6:88043537-88043835	K562	blood:	n/a	chr6:88043739-88043749
32	MAX	chr6:88043530-88043842	K562	blood:	n/a	chr6:88043739-88043749
33	MAX	chr6:88042808-88042953	K562	blood:	n/a	chr6:88042879-88042889
34	MAX	chr6:88043588-88043914	NB4	blood:	n/a	chr6:88043739-88043749
35	MAX	chr6:88042679-88042978	H1-hESC	embryonic stem cell:	n/a	chr6:88042879-88042889
36	MAX	chr6:88042808-88043000	NB4	blood:	n/a	chr6:88042879-88042889
37	MAX	chr6:88042667-88043081	H1-hESC	embryonic stem cell:	n/a	chr6:88042879-88042889
38	MYC	chr6:88043571-88043793	K562	blood:	n/a	chr6:88043739-88043749
39	MYC	chr6:88043487-88043712	MCF10A-Er-Src	breast:	n/a	n/a
40	MYC	chr6:88038737-88038798	MCF-7	breast:	n/a	n/a
41	MYC	chr6:88038582-88038671	MCF-7	breast:	n/a	n/a
42	MYC	chr6:88043716-88043841	NB4	blood:	n/a	chr6:88043739-88043749
43	MYC	chr6:88043484-88043651	MCF10A-Er-Src	breast:	n/a	n/a
44	MYC	chr6:88038538-88038884	MCF-7	breast:	n/a	n/a
45	MYC	chr6:88042809-88043035	K562	blood:	n/a	chr6:88042879-88042889
46	POLR2A	chr6:88038686-88038711	MCF-7	breast:	n/a	n/a
47	POLR2A	chr6:88038995-88039003	MCF-7	breast:	n/a	n/a
48	POLR2A	chr6:88039077-88039088	MCF-7	breast:	n/a	n/a
49	POLR2A	chr6:88038438-88038718	MCF-7	breast:	n/a	n/a
50	POLR2A	chr6:88038590-88038665	MCF-7	breast:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:88040249-88040299	AG10803	skin:	n/a
2	chr6:88040249-88040299	AG10803	skin:	n/a
3	chr6:88039504-88039554	Hela-S3	cervix:	n/a
4	chr6:88039023-88039073	NB4	blood:	n/a
5	chr6:88039031-88039081	IMR90	lung:	fetal
6	chr6:88039504-88039554	HCT-116	colon:	n/a
7	chr6:88039504-88039554	K562	blood:	n/a
8	chr6:88039031-88039081	U87	brain:	n/a
9	chr6:88039031-88039081	HAEpiC	amniotic membrane:	n/a
10	chr6:88039031-88039081	HEEpiC	esophagus:	n/a
11	chr6:88040249-88040299	SK-N-SH_RA	brain:	n/a
12	chr6:88040249-88040299	HEK293	kidney:	embryo
13	chr6:88039023-88039073	AoSMC	blood vessel:	n/a
14	chr6:88039031-88039081	ProgFib	skin:	n/a
15	chr6:88040249-88040299	NHBE	bronchial:	n/a
16	chr6:88039504-88039554	AoSMC	blood vessel:	n/a
17	chr6:88039023-88039073	HPAEpiC	pulmonary alveolar:	n/a
18	chr6:88039023-88039073	K562	blood:	n/a
19	chr6:88039504-88039554	PANC-1	pancreas:	n/a
20	chr6:88039031-88039081	Caco-2	colon:	n/a
21	chr6:88039504-88039554	HEK293	kidney:	embryo
22	chr6:88039504-88039554	AG09309	skin:	n/a
23	chr6:88039504-88039554	LNCaP	prostate:	n/a
24	chr6:88039504-88039554	SK-N-MC	brain:	n/a
25	chr6:88039023-88039073	PFSK-1	brain:	n/a
26	chr6:88040249-88040299	Hela-S3	cervix:	n/a
27	chr6:88039504-88039554	HAEpiC	amniotic membrane:	n/a
28	chr6:88040249-88040299	AG09319	gingival:	n/a
29	chr6:88039504-88039554	GM06990	blood:	n/a
30	chr6:88039031-88039081	BE2_C	brain:	n/a
31	chr6:88039504-88039554	AG04449	skin:	fetal
32	chr6:88040249-88040299	HPAEpiC	pulmonary alveolar:	n/a
33	chr6:88039504-88039554	SAEC	small airway:	n/a
34	chr6:88039023-88039073	MCF-7	breast:	n/a
35	chr6:88040249-88040299	PANC-1	pancreas:	n/a
36	chr6:88039504-88039554	ProgFib	skin:	n/a
37	chr6:88039031-88039081	Jurkat	blood:	n/a
38	chr6:88040249-88040299	GM19239	blood:	n/a
39	chr6:88039504-88039554	GM19239	blood:	n/a
40	chr6:88039504-88039554	HCF	heart:	n/a
41	chr6:88039031-88039081	HepG2	liver:	n/a
42	chr6:88039031-88039081	PFSK-1	brain:	n/a
43	chr6:88040249-88040299	AoSMC	blood vessel:	n/a
44	chr6:88039023-88039073	AG09319	gingival:	n/a
45	chr6:88039031-88039081	HCT-116	colon:	n/a
46	chr6:88040249-88040299	HCM	heart:	n/a
47	chr6:88039031-88039081	H1-hESC	embryonic stem cell:	embryo
48	chr6:88039023-88039073	NT2-D1	testis:	n/a
49	chr6:88040249-88040299	SAEC	small airway:	n/a
50	chr6:88040249-88040299	HAEpiC	amniotic membrane:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:88041023..88043490-chr6:88050888..88053357,2	K562	blood:
2	chr6:88044455..88046283-chr6:88047721..88049403,2	K562	blood:
3	chr6:88031398..88035229-chr6:88037396..88042297,5	MCF-7	breast:
4	chr6:88030655..88033234-chr6:88038071..88039593,2	MCF-7	breast:
5	chr6:88040776..88043456-chr6:88056096..88058777,2	MCF-7	breast:
6	chr6:88032389..88034079-chr6:88038245..88041213,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RARS2-5	chr6:88038856-88038959	NONHSAT113898

No data

Variant related genes	Relation type
GJB7	TF binding region
GJB7	CpG island
ENSG00000164411	chromatin interactions
ENSG00000111850	chromatin interactions
ENSG00000203872	chromatin interactions
ENSG00000226524	chromatin interactions

Extended variants
information (count: 241 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:241 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543611454	chr6:88038572-88038573	Active TSS Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs184116732	chr6:88038577-88038578	Active TSS Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs577101201	chr6:88038578-88038579	Active TSS Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs28890862	chr6:88038584-88038585	Active TSS Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs190817343	chr6:88038590-88038591	Active TSS Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs182314049	chr6:88038626-88038627	Active TSS Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs542721397	chr6:88038631-88038632	Active TSS Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs143115787	chr6:88038639-88038640	Active TSS Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs531672725	chr6:88038664-88038665	Active TSS Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs151199208	chr6:88038694-88038695	Active TSS Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs141397477	chr6:88038701-88038702	Active TSS Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs186623083	chr6:88038711-88038712	Active TSS Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs147011459	chr6:88038735-88038736	Active TSS Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs138243989	chr6:88038741-88038742	Active TSS Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs536222124	chr6:88038798-88038799	Active TSS Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs73488017	chr6:88038822-88038823	Active TSS Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs569792589	chr6:88038825-88038826	Active TSS Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs552800858	chr6:88038835-88038836	Active TSS Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs116724056	chr6:88038841-88038842	Active TSS Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs538478409	chr6:88038843-88038844	Active TSS Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs114519347	chr6:88038844-88038845	Active TSS Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs71572749	chr6:88038856-88038857	Active TSS Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
23	rs571724564	chr6:88038894-88038895	Active TSS Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
24	rs193008033	chr6:88038895-88038896	Active TSS Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
25	rs552807784	chr6:88038902-88038903	Active TSS Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
26	rs572124013	chr6:88038923-88038924	Active TSS Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
27	rs58321177	chr6:88038961-88038962	Active TSS Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs560931451	chr6:88039023-88039024	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs182790561	chr6:88039032-88039033	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs60628059	chr6:88039049-88039050	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs188692527	chr6:88039055-88039056	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs532558663	chr6:88039062-88039063	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs548087845	chr6:88039063-88039064	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs566350704	chr6:88039117-88039118	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs192832169	chr6:88039139-88039140	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs548239491	chr6:88039141-88039142	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs184998077	chr6:88039178-88039179	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs116406933	chr6:88039203-88039204	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs558322827	chr6:88039205-88039206	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs72391962	chr6:88039217-88039218	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs60776882	chr6:88039230-88039231	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs548753846	chr6:88039248-88039249	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs189572632	chr6:88039272-88039273	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs57596999	chr6:88039304-88039305	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs552871703	chr6:88039310-88039311	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs574426621	chr6:88039377-88039378	Active TSS Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs368831757	chr6:88039409-88039410	Active TSS Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs145953174	chr6:88039416-88039417	Active TSS Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs554588984	chr6:88039424-88039425	Active TSS Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs568637080	chr6:88039426-88039427	Active TSS Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:105)

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
Acute lymphoblastic leukemia	20067559	CNVD
Systemic lupus erythematosus	17503323	CNVD
Melanoma	18172304	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
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
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
abnormal development	18461090	CNVD
Myelodysplastic syndrome	18508791	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	21364760	CNVD
Developmental delay	19490664	CNVD
Myelofibrosis	22110671	CNVD
Urothelial cell carcinoma	18451213	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD

Chromatin state (count:191 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:88033000-88039600	Weak transcription	GM12878-XiMat	blood
2	chr6:88033000-88043600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr6:88033000-88043600	Weak transcription	Fetal Intestine Small	intestine
4	chr6:88033000-88043600	Weak transcription	Spleen	Spleen
5	chr6:88033000-88049000	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr6:88033000-88055200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr6:88033200-88042800	Weak transcription	Fetal Thymus	thymus
8	chr6:88033200-88043000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr6:88033200-88043400	Weak transcription	Primary T cells from cord blood	blood
10	chr6:88033200-88043600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
11	chr6:88033200-88043600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr6:88033200-88043600	Weak transcription	Pancreas	Pancrea
13	chr6:88033200-88045200	Weak transcription	Stomach Smooth Muscle	stomach
14	chr6:88033200-88045400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr6:88033200-88048000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
16	chr6:88033200-88056400	Weak transcription	Liver	Liver
17	chr6:88033200-88062200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
18	chr6:88035800-88043400	Weak transcription	Primary hematopoietic stem cells	blood
19	chr6:88038000-88039000	Active TSS	iPS-20b Cell Line	embryonic stem cell
20	chr6:88038000-88039600	Active TSS	ES-I3 Cell Line	embryonic stem cell
21	chr6:88038200-88038600	Enhancers	H1 Cell Line	embryonic stem cell
22	chr6:88038200-88038600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr6:88038200-88039000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr6:88038200-88039000	Active TSS	iPS-18 Cell Line	embryonic stem cell
25	chr6:88038200-88039200	Active TSS	HUES64 Cell Line	embryonic stem cell
26	chr6:88038200-88039400	Active TSS	iPS-15b Cell Line	embryonic stem cell
27	chr6:88038400-88039200	Active TSS	H9 Cell Line	embryonic stem cell
28	chr6:88038400-88039400	Active TSS	HUES6 Cell Line	embryonic stem cell
29	chr6:88038600-88038800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr6:88038600-88038800	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
31	chr6:88038600-88039000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
32	chr6:88038600-88039000	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr6:88038600-88039000	Active TSS	Hela-S3	cervix
34	chr6:88038600-88039200	Flanking Active TSS	H1 Cell Line	embryonic stem cell
35	chr6:88038600-88039200	Active TSS	HUES48 Cell Line	embryonic stem cell
36	chr6:88038600-88039400	Active TSS	Placenta	Placenta
37	chr6:88038800-88039000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr6:88038800-88039000	Flanking Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr6:88038800-88042600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
40	chr6:88039000-88039200	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr6:88039000-88039400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr6:88039000-88042400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr6:88039000-88042400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
44	chr6:88039000-88042800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
45	chr6:88039000-88042800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr6:88039000-88044200	Weak transcription	Hela-S3	cervix
47	chr6:88039000-88051400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr6:88039000-88068400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr6:88039000-88078400	Weak transcription	Fetal Stomach	stomach
50	chr6:88039200-88039400	Enhancers	H1 Cell Line	embryonic stem cell

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