Variant report

Variant	esv2753902
Chromosome Location	chr6:93671679-93994779
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:707)
CpG islands
(count:305)
Chromatin interactive
region (count:32)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:8)

(count:707 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr6:93785785-93785808	K562	blood:	n/a	n/a
2	BACH1	chr6:93799001-93799008	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr6:93885797-93886081	GM12878	blood:	n/a	n/a
4	BATF	chr6:93750187-93750453	GM12878	blood:	n/a	chr6:93750353-93750364
5	BATF	chr6:93849197-93849443	GM12878	blood:	n/a	chr6:93849351-93849360
6	BATF	chr6:93849138-93849535	GM12878	blood:	n/a	chr6:93849351-93849360
7	BATF	chr6:93885853-93886047	GM12878	blood:	n/a	n/a
8	BCL11A	chr6:93758218-93758355	H1-hESC	embryonic stem cell:	n/a	chr6:93758327-93758336
9	BHLHE40	chr6:93885755-93886044	GM12878	blood:	n/a	n/a
10	BRCA1	chr6:93794796-93794805	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr6:93814705-93815211	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr6:93833986-93834289	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr6:93829925-93830101	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr6:93833971-93834305	HepG2	liver:	n/a	n/a
15	CEBPB	chr6:93718968-93719168	A549	lung:	n/a	chr6:93719075-93719086
16	CEBPB	chr6:93833987-93834325	MCF-7	breast:	n/a	n/a
17	CEBPB	chr6:93733269-93733607	HepG2	liver:	n/a	chr6:93733424-93733435
18	CEBPB	chr6:93746552-93746865	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr6:93677242-93677465	MCF-7	breast:	n/a	n/a
20	CEBPB	chr6:93779601-93779920	HepG2	liver:	n/a	chr6:93779769-93779780
21	CEBPB	chr6:93867258-93867339	HepG2	liver:	n/a	chr6:93867287-93867298
22	CEBPB	chr6:93814816-93815086	MCF-7	breast:	n/a	n/a
23	CEBPB	chr6:93887484-93887810	HepG2	liver:	n/a	chr6:93887635-93887648 chr6:93887635-93887646
24	CEBPB	chr6:93699464-93699671	HepG2	liver:	n/a	chr6:93699569-93699580
25	CEBPB	chr6:93689226-93689514	HepG2	liver:	n/a	chr6:93689387-93689398 chr6:93689447-93689459 chr6:93689388-93689397
26	CEBPB	chr6:93950461-93950774	IMR90	lung:	n/a	n/a
27	CEBPB	chr6:93887561-93887838	Hela-S3	cervix:	n/a	chr6:93887635-93887648 chr6:93887635-93887646
28	CEBPB	chr6:93950501-93950774	A549	lung:	n/a	n/a
29	CEBPB	chr6:93834038-93834167	HepG2	liver:	n/a	n/a
30	CEBPB	chr6:93950465-93950793	HepG2	liver:	n/a	n/a
31	CEBPB	chr6:93779657-93779870	H1-hESC	embryonic stem cell:	n/a	chr6:93779769-93779780
32	CEBPB	chr6:93938655-93938699	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr6:93718900-93719253	Hela-S3	cervix:	n/a	chr6:93719217-93719230 chr6:93719075-93719086 chr6:93719219-93719230
34	CEBPB	chr6:93950504-93950792	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr6:93822839-93823017	Hela-S3	cervix:	n/a	chr6:93822903-93822914
36	CEBPB	chr6:93822826-93823016	H1-hESC	embryonic stem cell:	n/a	chr6:93822903-93822914
37	CEBPB	chr6:93677191-93677391	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr6:93733299-93733596	IMR90	lung:	n/a	chr6:93733424-93733435
39	CEBPB	chr6:93890196-93890517	Hela-S3	cervix:	n/a	chr6:93890366-93890379 chr6:93890368-93890377 chr6:93890366-93890379 chr6:93890368-93890379
40	CEBPB	chr6:93804885-93805100	A549	lung:	n/a	chr6:93804950-93804961 chr6:93804984-93804995
41	CEBPB	chr6:93822843-93823065	HepG2	liver:	n/a	chr6:93822903-93822914
42	CEBPB	chr6:93876292-93876557	HepG2	liver:	n/a	chr6:93876420-93876431
43	CEBPB	chr6:93850996-93851093	HepG2	liver:	n/a	chr6:93851025-93851036
44	CEBPB	chr6:93804861-93805074	HepG2	liver:	n/a	chr6:93804950-93804961 chr6:93804984-93804995
45	CEBPB	chr6:93718928-93719146	HepG2	liver:	n/a	chr6:93719075-93719086
46	CEBPB	chr6:93892774-93893405	Hela-S3	cervix:	n/a	chr6:93893208-93893219
47	CEBPB	chr6:93833964-93834316	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr6:93779643-93779885	A549	lung:	n/a	chr6:93779769-93779780
49	CEBPB	chr6:93779629-93779927	IMR90	lung:	n/a	chr6:93779769-93779780
50	CEBPB	chr6:93689988-93690188	HepG2	liver:	n/a	chr6:93690080-93690091

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:93992415-93992465	H1-hESC	embryonic stem cell:	embryo
2	chr6:93887573-93887623	HMEC	breast:	n/a
3	chr6:93992415-93992465	T-47D	breast:	n/a
4	chr6:93992415-93992465	HCPEpiC	choroid plexus:	n/a
5	chr6:93789928-93789978	HCM	heart:	n/a
6	chr6:93887573-93887623	AG09319	gingival:	n/a
7	chr6:93992464-93992514	HAEpiC	amniotic membrane:	n/a
8	chr6:93887573-93887623	U87	brain:	n/a
9	chr6:93789928-93789978	HUVEC	blood vessel:	n/a
10	chr6:93992417-93992467	NH-A	brain:	n/a
11	chr6:93992464-93992514	AG09309	skin:	n/a
12	chr6:93992417-93992467	PFSK-1	brain:	n/a
13	chr6:93992417-93992467	A549	lung:	n/a
14	chr6:93992415-93992465	AG10803	skin:	n/a
15	chr6:93992415-93992465	AG04449	skin:	fetal
16	chr6:93992415-93992465	HCF	heart:	n/a
17	chr6:93992417-93992467	PrEC	prostate:	n/a
18	chr6:93789928-93789978	NH-A	brain:	n/a
19	chr6:93992415-93992465	AG09319	gingival:	n/a
20	chr6:93992417-93992467	HEK293	kidney:	embryo
21	chr6:93992464-93992514	SK-N-SH	brain:	n/a
22	chr6:93992415-93992465	SK-N-SH_RA	brain:	n/a
23	chr6:93992417-93992467	GM12891	blood:	n/a
24	chr6:93789928-93789978	Caco-2	colon:	n/a
25	chr6:93992464-93992514	NHDF-neo	bronchial:	n/a
26	chr6:93887573-93887623	GM12892	blood:	n/a
27	chr6:93789928-93789978	ovcar-3	ovarian:	n/a
28	chr6:93992417-93992467	HRE	kidney:	n/a
29	chr6:93992417-93992467	GM12878	blood:	n/a
30	chr6:93992464-93992514	HepG2	liver:	n/a
31	chr6:93887573-93887623	PFSK-1	brain:	n/a
32	chr6:93992464-93992514	BE2_C	brain:	n/a
33	chr6:93992415-93992465	SK-N-SH	brain:	n/a
34	chr6:93992415-93992465	HUVEC	blood vessel:	n/a
35	chr6:93789928-93789978	Hepatocyte	liver:	n/a
36	chr6:93789928-93789978	PANC-1	pancreas:	n/a
37	chr6:93992464-93992514	LNCaP	prostate:	n/a
38	chr6:93992417-93992467	NT2-D1	testis:	n/a
39	chr6:93992415-93992465	HEK293	kidney:	embryo
40	chr6:93992415-93992465	HL-60	blood:	n/a
41	chr6:93887573-93887623	HPAEpiC	pulmonary alveolar:	n/a
42	chr6:93992417-93992467	ProgFib	skin:	n/a
43	chr6:93992464-93992514	HL-60	blood:	n/a
44	chr6:93992417-93992467	PANC-1	pancreas:	n/a
45	chr6:93992417-93992467	GM06990	blood:	n/a
46	chr6:93992417-93992467	SK-N-SH	brain:	n/a
47	chr6:93789928-93789978	SAEC	small airway:	n/a
48	chr6:93887573-93887623	SK-N-SH_RA	brain:	n/a
49	chr6:93992464-93992514	MCF-7	breast:	n/a
50	chr6:93992464-93992514	HUVEC	blood vessel:	n/a

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:93809738..93811467-chr6:93820413..93822351,2	K562	blood:
2	chr6:93691182..93692729-chr6:93694302..93697274,2	K562	blood:
3	chr6:93913223..93915449-chr6:93919354..93921018,2	MCF-7	breast:
4	chr6:93876478..93878612-chr6:94124255..94126715,2	MCF-7	breast:
5	chr6:93780261..93783234-chr6:93783302..93785531,2	MCF-7	breast:
6	chr6:93945747..93948325-chr6:93957939..93959736,2	K562	blood:
7	chr6:93914152..93916093-chr6:93916123..93918942,2	MCF-7	breast:
8	chr6:93749711..93751923-chr6:93752867..93755308,2	MCF-7	breast:
9	chr6:93698868..93701522-chr6:93703182..93705134,2	MCF-7	breast:
10	chr6:93897520..93899127-chr6:93900118..93901832,2	MCF-7	breast:
11	chr6:93780261..93783234-chr6:93783302..93785531,2	MCF-7	breast:
12	chr6:93721414..93723700-chr6:93724604..93727201,3	MCF-7	breast:
13	chr6:93721414..93723700-chr6:93724604..93727201,3	MCF-7	breast:
14	chr6:93824925..93826754-chr6:93831718..93833300,2	MCF-7	breast:
15	chr6:93816179..93818015-chr6:93819610..93821560,2	MCF-7	breast:
16	chr6:93931036..93933172-chr6:94009352..94011662,2	MCF-7	breast:
17	chr6:93809738..93811467-chr6:93820413..93822351,2	K562	blood:
18	chr6:93816179..93818015-chr6:93819610..93821560,2	MCF-7	breast:
19	chr6:93691182..93692729-chr6:93694302..93697274,2	K562	blood:
20	chr6:93824925..93826754-chr6:93831718..93833300,2	MCF-7	breast:
21	chr6:93892704..93894556-chr6:93953207..93955566,2	K562	blood:
22	chr6:93797134..93798758-chr6:94127992..94129499,2	MCF-7	breast:
23	chr6:93749711..93751923-chr6:93752867..93755308,2	MCF-7	breast:
24	chr6:93973793..93974315-chr8:123979961..123980768,2	MCF-7	breast:
25	chr6:93698868..93701522-chr6:93703182..93705134,2	MCF-7	breast:
26	chr6:93945747..93948325-chr6:93957939..93959736,2	K562	blood:
27	chr6:93913223..93915449-chr6:93919354..93921018,2	MCF-7	breast:
28	chr6:93520687..93521206-chr6:93726686..93727450,3	MCF-7	breast:
29	chr6:93897520..93899127-chr6:93900118..93901832,2	MCF-7	breast:
30	chr6:93892704..93894556-chr6:93953207..93955566,2	K562	blood:
31	chr12:54136317..54137172-chr6:93686043..93686596,2	MCF-7	breast:
32	chr6:93914152..93916093-chr6:93916123..93918942,2	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MANEA-5	chr6:93695711-93695847	NONHSAT114018
2	lnc-MANEA-4	chr6:93780105-93780248	ENSG00000235099
3	lnc-MANEA-5	chr6:93690972-93691115	XLOC_005389
4	lnc-MANEA-5	chr6:93689707-93689741	NONHSAT114018
5	lnc-MANEA-4	chr6:93812508-93813102	ENSG00000235099
6	lnc-MANEA-5	chr6:93689708-93689741	XLOC_005389
7	lnc-MANEA-5	chr6:93695712-93695847	XLOC_005389
8	lnc-MANEA-5	chr6:93690971-93691115	NONHSAT114018

No data

(count:8 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	EPHA7	hsa-miR-196a-5p	chr6:93952900-93952922
2	EPHA7	hsa-miR-93-5p	chr6:93952361-93952384
3	EPHA7	hsa-miR-125b-5p	chr6:93950445-93950465
4	EPHA7	hsa-miR-196a-5p	chr6:93952906-93952900
5	EPHA7	hsa-miR-93-5p	chr6:93952367-93952361
6	EPHA7	hsa-miR-93-5p	chr6:93951073-93951066
7	EPHA7	hsa-miR-93-5p	chr6:93951488-93951512
8	EPHA7	hsa-miR-93-5p	chr6:93951067-93951092

Variant related genes	Relation type
ENSG00000235099	TF binding region
COPS5P1	TF binding region
ENSG00000235099	CpG island
COPS5P1	CpG island
ENSG00000135333	chromatin interactions
ZNF236	miRNA target sites
EDEM3	miRNA target sites
UPF2	miRNA target sites

Extended variants
information (count: 7822 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:7822 , 50 per page) page: 1 2 3 4 5 6 7 ... 157

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs377010749	chr6:93672874-93672875	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs534396285	chr6:93672893-93672894	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs57211993	chr6:93672906-93672907	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs577193268	chr6:93672948-93672949	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs150113433	chr6:93672953-93672954	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs548955738	chr6:93672971-93672972	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs567854686	chr6:93672972-93672973	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs189861054	chr6:93673005-93673006	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs35472176	chr6:93673021-93673022	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs34088201	chr6:93673036-93673037	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs536718656	chr6:93673084-93673085	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs138552715	chr6:93673129-93673130	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs7742297	chr6:93673175-93673176	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs539064279	chr6:93673177-93673178	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs568979495	chr6:93673187-93673188	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs534254006	chr6:93674034-93674035	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs572426261	chr6:93674070-93674071	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs1361177	chr6:93674075-93674076	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs554066224	chr6:93674081-93674082	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs374431363	chr6:93674113-93674114	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs573476418	chr6:93674153-93674154	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs368690609	chr6:93674211-93674212	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs542459042	chr6:93674232-93674233	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs530146217	chr6:93674238-93674239	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs144181215	chr6:93674246-93674247	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs76204514	chr6:93674355-93674356	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs34356963	chr6:93674390-93674391	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs545092401	chr6:93674419-93674420	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs17528777	chr6:93674438-93674439	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs527300174	chr6:93674451-93674452	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs541347021	chr6:93674469-93674470	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs537852361	chr6:93674472-93674473	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs561597399	chr6:93674482-93674483	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs201929540	chr6:93674560-93674561	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs142192956	chr6:93674567-93674568	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs151061367	chr6:93674612-93674613	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs570264434	chr6:93674689-93674690	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs140828724	chr6:93674697-93674698	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs552654758	chr6:93674711-93674712	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs111669667	chr6:93674786-93674787	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs574146857	chr6:93674815-93674816	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs17437983	chr6:93674832-93674833	Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
43	rs377149425	chr6:93674931-93674932	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs2485797	chr6:93674940-93674941	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs144588327	chr6:93674953-93674954	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs555895362	chr6:93674965-93674966	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs575856046	chr6:93675003-93675004	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs143199424	chr6:93675090-93675091	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs369518438	chr6:93675107-93675108	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs544973750	chr6:93675108-93675109	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:106)

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
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
Prostate cancer	18632612	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	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	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	17640729	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	21364760	CNVD
Developmental delay	19490664	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Adrenocortical carcinoma	18281524	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Neuropathy	19664229	CNVD
Neurodevelopmental disorder	22521361	CNVD
Burkitt''s lymphoma	18698080	CNVD
Ovarian cancer	21720365	CNVD
Basal cell lymphoma	17170743	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Epilepsy	22083797	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD

Chromatin state (count:616 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:93672800-93673200	Enhancers	Fetal Brain Female	brain
2	chr6:93674000-93675600	Enhancers	Fetal Heart	heart
3	chr6:93677200-93677400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr6:93686000-93686400	Enhancers	Small Intestine	intestine
5	chr6:93686000-93687800	Enhancers	Duodenum Mucosa	Duodenum
6	chr6:93686400-93688800	Weak transcription	Small Intestine	intestine
7	chr6:93686600-93687200	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr6:93687800-93689000	Weak transcription	Duodenum Mucosa	Duodenum
9	chr6:93688400-93689400	Enhancers	HUVEC	blood vessel
10	chr6:93688600-93689600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
11	chr6:93688800-93689600	Enhancers	Fetal Heart	heart
12	chr6:93688800-93689600	Enhancers	Small Intestine	intestine
13	chr6:93689000-93689400	Enhancers	Duodenum Mucosa	Duodenum
14	chr6:93689400-93694600	Weak transcription	Duodenum Mucosa	Duodenum
15	chr6:93694600-93695800	Enhancers	Duodenum Mucosa	Duodenum
16	chr6:93697800-93698000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr6:93698000-93699000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr6:93699000-93700200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr6:93699200-93700000	Enhancers	NH-A	brain
20	chr6:93699400-93700000	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr6:93722400-93722800	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr6:93722400-93723200	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr6:93722600-93723000	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr6:93726800-93727000	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr6:93726800-93727200	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr6:93727200-93730600	Weak transcription	HUES6 Cell Line	embryonic stem cell
27	chr6:93730600-93731600	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr6:93730800-93732200	Enhancers	Fetal Brain Female	brain
29	chr6:93730800-93732400	Enhancers	Fetal Brain Male	brain
30	chr6:93740800-93746800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr6:93746800-93747200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr6:93746800-93747400	ZNF genes & repeats	Gastric	stomach
33	chr6:93746800-93747600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr6:93747000-93747600	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr6:93747800-93748000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
36	chr6:93748000-93754200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr6:93748600-93750000	Enhancers	HUVEC	blood vessel
38	chr6:93748800-93750400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
39	chr6:93749000-93750000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr6:93749000-93751200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr6:93749400-93751800	Enhancers	Primary hematopoietic stem cells short term culture	blood
42	chr6:93749600-93750600	Enhancers	Primary monocytes fromperipheralblood	blood
43	chr6:93749600-93750800	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr6:93749800-93750200	Enhancers	Monocytes-CD14+_RO01746	blood
45	chr6:93749800-93750600	Enhancers	H9 Cell Line	embryonic stem cell
46	chr6:93749800-93750800	Enhancers	Primary hematopoietic stem cells	blood
47	chr6:93750000-93750400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr6:93750000-93750400	Flanking Active TSS	HUVEC	blood vessel
49	chr6:93750000-93750600	Enhancers	iPS-20b Cell Line	embryonic stem cell
50	chr6:93750000-93750600	Enhancers	NH-A	brain

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