Variant report

Variant	esv3473881
Chromosome Location	chr6:29916964-29938022
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1093)
CpG islands
(count:1709)
Chromatin interactive
region (count:32)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1093 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:29937042-29937091	K562	blood:	n/a	n/a
2	ARID3A	chr6:29933775-29934240	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:29932290-29932954	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:29935252-29935904	K562	blood:	n/a	n/a
5	ARID3A	chr6:29932477-29933236	K562	blood:	n/a	n/a
6	ARID3A	chr6:29931139-29931164	K562	blood:	n/a	n/a
7	ARID3A	chr6:29934522-29934914	K562	blood:	n/a	n/a
8	ARID3A	chr6:29933748-29934309	K562	blood:	n/a	n/a
9	ARID3A	chr6:29935249-29935871	HepG2	liver:	n/a	n/a
10	ARID3A	chr6:29922852-29922901	K562	blood:	n/a	n/a
11	ATF1	chr6:29932584-29933076	K562	blood:	n/a	n/a
12	ATF1	chr6:29935286-29935585	K562	blood:	n/a	n/a
13	ATF2	chr6:29932488-29932978	GM12878	blood:	n/a	n/a
14	ATF2	chr6:29932433-29933091	GM12878	blood:	n/a	n/a
15	ATF3	chr6:29932539-29933023	K562	blood:	n/a	n/a
16	ATF3	chr6:29932615-29932943	K562	blood:	n/a	n/a
17	BACH1	chr6:29932608-29933062	K562	blood:	n/a	n/a
18	BACH1	chr6:29932453-29933278	H1-hESC	embryonic stem cell:	n/a	n/a
19	BATF	chr6:29932589-29933017	GM12878	blood:	n/a	chr6:29932797-29932808 chr6:29932798-29932808
20	BATF	chr6:29932612-29932987	GM12878	blood:	n/a	chr6:29932797-29932808 chr6:29932798-29932808
21	BCL11A	chr6:29932639-29932881	GM12878	blood:	n/a	chr6:29932797-29932806
22	BCL11A	chr6:29932602-29932969	GM12878	blood:	n/a	chr6:29932797-29932806
23	BCL3	chr6:29932533-29932943	GM12878	blood:	n/a	chr6:29932797-29932806
24	BCLAF1	chr6:29932428-29933119	GM12878	blood:	n/a	chr6:29932797-29932806
25	BCLAF1	chr6:29932494-29933203	GM12878	blood:	n/a	chr6:29932797-29932806
26	BHLHE40	chr6:29932569-29933159	K562	blood:	n/a	n/a
27	BHLHE40	chr6:29934607-29934610	GM12878	blood:	n/a	n/a
28	BHLHE40	chr6:29933714-29934091	HepG2	liver:	n/a	n/a
29	BHLHE40	chr6:29920974-29921274	K562	blood:	n/a	n/a
30	BHLHE40	chr6:29932548-29933279	GM12878	blood:	n/a	n/a
31	BHLHE40	chr6:29933866-29934118	GM12878	blood:	n/a	n/a
32	BHLHE40	chr6:29933686-29934301	K562	blood:	n/a	n/a
33	BHLHE40	chr6:29935166-29935758	K562	blood:	n/a	n/a
34	BHLHE40	chr6:29920783-29921023	A549	lung:	n/a	n/a
35	CBX3	chr6:29935860-29936460	HCT-116	colon:	n/a	n/a
36	CBX3	chr6:29920575-29921454	HCT-116	colon:	n/a	n/a
37	CBX3	chr6:29932608-29932997	K562	blood:	n/a	n/a
38	CBX3	chr6:29933685-29934511	HCT-116	colon:	n/a	n/a
39	CBX3	chr6:29935109-29935665	K562	blood:	n/a	n/a
40	CBX3	chr6:29932504-29933475	K562	blood:	n/a	n/a
41	CBX3	chr6:29932403-29933273	HCT-116	colon:	n/a	n/a
42	CBX3	chr6:29935905-29936437	HCT-116	colon:	n/a	n/a
43	CCNT2	chr6:29932623-29932970	K562	blood:	n/a	n/a
44	CCNT2	chr6:29935317-29935569	K562	blood:	n/a	n/a
45	CEBPB	chr6:29936002-29936359	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr6:29933654-29933956	HepG2	liver:	n/a	n/a
47	CEBPB	chr6:29935138-29935549	K562	blood:	n/a	chr6:29935249-29935260 chr6:29935210-29935221
48	CEBPB	chr6:29934230-29934543	IMR90	lung:	n/a	n/a
49	CEBPB	chr6:29932426-29933189	K562	blood:	n/a	n/a
50	CEBPB	chr6:29932451-29933116	GM12878	blood:	n/a	n/a

(count:1709 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:29924202-29924252	LNCaP	prostate:	n/a
2	chr6:29924202-29924252	LNCaP	prostate:	n/a
3	chr6:29928362-29928412	ECC-1	luminal epithelium:	n/a
4	chr6:29932743-29932793	Jurkat	blood:	n/a
5	chr6:29924299-29924349	SK-N-MC	brain:	n/a
6	chr6:29924299-29924349	BJ	skin:	n/a
7	chr6:29924202-29924252	K562	blood:	n/a
8	chr6:29924471-29924521	HCT-116	colon:	n/a
9	chr6:29923952-29924002	BE2_C	brain:	n/a
10	chr6:29924299-29924349	HCF	heart:	n/a
11	chr6:29933697-29933747	RPTEC	kidney:	n/a
12	chr6:29932621-29932671	NH-A	brain:	n/a
13	chr6:29924471-29924521	Hepatocyte	liver:	n/a
14	chr6:29923954-29924004	MCF-7	breast:	n/a
15	chr6:29924475-29924525	AG09319	gingival:	n/a
16	chr6:29932743-29932793	AG10803	skin:	n/a
17	chr6:29924067-29924117	GM12892	blood:	n/a
18	chr6:29933925-29933975	HCM	heart:	n/a
19	chr6:29924247-29924297	GM12878	blood:	n/a
20	chr6:29933697-29933747	SK-N-SH	brain:	n/a
21	chr6:29924299-29924349	NB4	blood:	n/a
22	chr6:29932743-29932793	PANC-1	pancreas:	n/a
23	chr6:29924310-29924360	NHBE	bronchial:	n/a
24	chr6:29921779-29921829	SK-N-SH_RA	brain:	n/a
25	chr6:29923913-29923963	AoSMC	blood vessel:	n/a
26	chr6:29922522-29922572	ovcar-3	ovarian:	n/a
27	chr6:29933511-29933561	CMK	blood:	n/a
28	chr6:29924475-29924525	Caco-2	colon:	n/a
29	chr6:29924299-29924349	SK-N-SH_RA	brain:	n/a
30	chr6:29933697-29933747	Jurkat	blood:	n/a
31	chr6:29924407-29924457	NT2-D1	testis:	n/a
32	chr6:29922522-29922572	HMEC	breast:	n/a
33	chr6:29924067-29924117	SKMC	muscle:	n/a
34	chr6:29924202-29924252	IMR90	lung:	fetal
35	chr6:29932621-29932671	NB4	blood:	n/a
36	chr6:29933411-29933461	ovcar-3	ovarian:	n/a
37	chr6:29924299-29924349	NH-A	brain:	n/a
38	chr6:29923952-29924002	GM19239	blood:	n/a
39	chr6:29923952-29924002	SK-N-SH	brain:	n/a
40	chr6:29924067-29924117	HMEC	breast:	n/a
41	chr6:29922522-29922572	ProgFib	skin:	n/a
42	chr6:29933511-29933561	HIPEpiC	eye:	n/a
43	chr6:29924067-29924117	PANC-1	pancreas:	n/a
44	chr6:29932864-29932914	Hepatocyte	liver:	n/a
45	chr6:29932743-29932793	GM12892	blood:	n/a
46	chr6:29923913-29923963	BJ	skin:	n/a
47	chr6:29928362-29928412	Hepatocyte	liver:	n/a
48	chr6:29933925-29933975	RPTEC	kidney:	n/a
49	chr6:29924407-29924457	HL-60	blood:	n/a
50	chr6:29932743-29932793	GM12891	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr6:29926306..29930004-chr6:29943804..29947247,3	K562	blood:
2	chr6:29927397..29931336-chr6:29932208..29936273,8	K562	blood:
3	chr6:29820057..29821697-chr6:29920603..29922626,2	K562	blood:
4	chr6:29820786..29821478-chr6:29935191..29935715,2	MCF-7	breast:
5	chr6:29917150..29919030-chr6:29920403..29922798,2	MCF-7	breast:
6	chr6:29937399..29939324-chr6:29949163..29951713,2	K562	blood:
7	chr6:29931653..29934276-chr6:29943760..29946372,5	K562	blood:
8	chr6:29929604..29934270-chr6:29942846..29948120,6	K562	blood:
9	chr6:29917977..29920432-chr6:29924161..29926474,2	K562	blood:
10	chr6:29917413..29919975-chr6:29932108..29934788,2	K562	blood:
11	chr6:29917413..29919975-chr6:29932108..29934788,2	K562	blood:
12	chr6:29937339..29939716-chr6:29942275..29944965,3	MCF-7	breast:
13	chr6:29920527..29922060-chr6:29926055..29928693,2	K562	blood:
14	chr6:29931972..29934794-chr6:30027595..30029471,2	K562	blood:
15	chr6:29921960..29924230-chr6:29934596..29936833,2	K562	blood:
16	chr6:29920547..29922811-chr6:29925895..29928597,2	MCF-7	breast:
17	chr6:29917150..29919030-chr6:29920403..29922798,2	MCF-7	breast:
18	chr6:29764926..29767618-chr6:29920990..29923179,3	MCF-7	breast:
19	chr6:29892582..29894711-chr6:29932418..29935205,2	K562	blood:
20	chr6:29931492..29933251-chr6:30034694..30036479,2	K562	blood:
21	chr6:29815528..29816550-chr6:29935117..29936165,4	MCF-7	breast:
22	chr6:29920547..29922811-chr6:29925895..29928597,2	MCF-7	breast:
23	chr6:29937696..29939359-chr6:30032545..30034517,2	K562	blood:
24	chr14:77247003..77248532-chr6:29931290..29933642,2	K562	blood:
25	chr6:29820931..29821695-chr6:29935492..29936150,2	MCF-7	breast:
26	chr6:29917426..29919477-chr6:29924161..29925991,2	K562	blood:
27	chr6:29932263..29935141-chr6:29936079..29939709,3	K562	blood:
28	chr6:29920527..29922060-chr6:29926055..29928693,2	K562	blood:
29	chr6:29927397..29931336-chr6:29932208..29936273,8	K562	blood:
30	chr6:29932263..29935141-chr6:29936079..29939709,3	K562	blood:
31	chr6:29933916..29936718-chr6:29943405..29945040,3	MCF-7	breast:
32	chr6:29921960..29924230-chr6:29934596..29936833,2	K562	blood:

No data

Variant related genes	Relation type
HCG9	TF binding region
HLA-W	TF binding region
HCG9	CpG island
HLA-W	CpG island
ENSG00000204625	chromatin interactions
ENSG00000259081	chromatin interactions
ENSG00000204623	chromatin interactions
ENSG00000066379	chromatin interactions
ENSG00000233265	chromatin interactions
ENSG00000204619	chromatin interactions
ENSG00000230795	chromatin interactions
ENSG00000235290	chromatin interactions

Extended variants
information (count: 1549 )
Associated
traits (count: 113 )

Variant overlapped rSNPs/rCNVs (count:1549 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs144774662	chr6:29916965-29916966	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs72845136	chr6:29916971-29916972	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs376183992	chr6:29916983-29916984	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs9260319	chr6:29916992-29916993	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs386698586	chr6:29917004-29917005	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs1655903	chr6:29917005-29917006	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs181126739	chr6:29917006-29917007	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs77309262	chr6:29917021-29917022	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs9260321	chr6:29917028-29917029	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
10	rs530938988	chr6:29917029-29917030	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs28894078	chr6:29917033-29917034	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
12	rs28894079	chr6:29917038-29917039	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
13	rs373886646	chr6:29917043-29917044	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs9260323	chr6:29917048-29917049	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
15	rs28749163	chr6:29917053-29917054	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
16	rs530710774	chr6:29917066-29917067	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs9260324	chr6:29917077-29917078	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
18	rs532427528	chr6:29917089-29917090	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs536445735	chr6:29917090-29917091	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs568811955	chr6:29917098-29917099	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs9260327	chr6:29917099-29917100	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs538303097	chr6:29917110-29917111	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs56369124	chr6:29917127-29917128	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs9260328	chr6:29917131-29917132	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs9260329	chr6:29917136-29917137	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs9260330	chr6:29917140-29917141	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs1655904	chr6:29917146-29917147	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs73725558	chr6:29917160-29917161	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs2517717	chr6:29917168-29917169	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs72845140	chr6:29917179-29917180	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs201611484	chr6:29917183-29917184	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs115514825	chr6:29917194-29917195	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs9260332	chr6:29917195-29917196	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs201737251	chr6:29917203-29917204	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs9260333	chr6:29917204-29917205	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs145062354	chr6:29917218-29917219	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs9260334	chr6:29917225-29917226	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs532121943	chr6:29917253-29917254	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs2517716	chr6:29917260-29917261	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs149112161	chr6:29917272-29917273	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs548205314	chr6:29917292-29917293	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs568204872	chr6:29917320-29917321	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs9260344	chr6:29917335-29917336	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs67940191	chr6:29917336-29917337	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs138435974	chr6:29917342-29917343	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs370679772	chr6:29917343-29917344	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs55858236	chr6:29917345-29917346	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs377152854	chr6:29917346-29917347	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs368899929	chr6:29917349-29917350	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs9260347	chr6:29917354-29917355	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance

Variant related diseases (count:113)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17133270	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21785460	CNVD
Retinoblastoma	16790693	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Schizophrenia	19571809	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
abnormal development	18461090	CNVD
Breast cancer	21509527	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Retinoblastoma	22278416	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Systemic lupus erythematosus	20877625	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Pancreatic cancer	17952125	CNVD
Glioma	20126413	CNVD

Chromatin state (count:851 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:29911200-29920200	Weak transcription	A549	lung
2	chr6:29911200-29921400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr6:29911600-29920400	Weak transcription	Fetal Brain Male	brain
4	chr6:29911800-29917200	Strong transcription	Fetal Stomach	stomach
5	chr6:29911800-29917600	Strong transcription	Fetal Intestine Large	intestine
6	chr6:29912400-29917200	Genic enhancers	Spleen	Spleen
7	chr6:29912400-29918000	Strong transcription	Fetal Intestine Small	intestine
8	chr6:29912600-29921000	Weak transcription	Psoas Muscle	Psoas
9	chr6:29912800-29924200	Weak transcription	Right Atrium	heart
10	chr6:29913000-29917200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr6:29913000-29924000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr6:29913000-29924200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr6:29913200-29917000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
14	chr6:29913200-29917000	Weak transcription	Brain Inferior Temporal Lobe	brain
15	chr6:29913400-29917000	Strong transcription	Stomach Smooth Muscle	stomach
16	chr6:29913400-29917800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
17	chr6:29913400-29917800	Weak transcription	Hela-S3	cervix
18	chr6:29913400-29918800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
19	chr6:29913400-29919600	Weak transcription	Fetal Muscle Trunk	muscle
20	chr6:29913400-29920800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr6:29913400-29932200	Weak transcription	Brain Anterior Caudate	brain
22	chr6:29913400-29932600	Weak transcription	Brain Substantia Nigra	brain
23	chr6:29913600-29917000	Weak transcription	HUES6 Cell Line	embryonic stem cell
24	chr6:29913600-29917200	Strong transcription	Duodenum Mucosa	Duodenum
25	chr6:29913600-29918800	Weak transcription	Muscle Satellite Cultured Cells	--
26	chr6:29913600-29919200	Weak transcription	HUES64 Cell Line	embryonic stem cell
27	chr6:29913600-29920400	Weak transcription	HMEC	breast
28	chr6:29913600-29921600	Weak transcription	NHEK	skin
29	chr6:29913600-29924400	Weak transcription	H1 Cell Line	embryonic stem cell
30	chr6:29913600-29925400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr6:29913800-29917200	Strong transcription	Adipose Nuclei	Adipose
32	chr6:29913800-29921000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr6:29913800-29932200	Weak transcription	Small Intestine	intestine
34	chr6:29914000-29917600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr6:29914000-29918000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
36	chr6:29914000-29918200	Strong transcription	Rectal Mucosa Donor 29	rectum
37	chr6:29914000-29918200	Strong transcription	Thymus	Thymus
38	chr6:29914000-29920600	Weak transcription	NHLF	lung
39	chr6:29914000-29921000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr6:29914000-29923800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr6:29914000-29924200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
42	chr6:29914000-29932200	Weak transcription	Colon Smooth Muscle	Colon
43	chr6:29914200-29918000	Genic enhancers	Primary T cells fromperipheralblood	blood
44	chr6:29914200-29918000	Strong transcription	Monocytes-CD14+_RO01746	blood
45	chr6:29914200-29918200	Strong transcription	Primary monocytes fromperipheralblood	blood
46	chr6:29914200-29919000	Strong transcription	Primary B cells from cord blood	blood
47	chr6:29914200-29919200	Weak transcription	HUES48 Cell Line	embryonic stem cell
48	chr6:29914200-29920800	Weak transcription	Cortex derived primary cultured neurospheres	brain
49	chr6:29914400-29917200	Strong transcription	Brain Hippocampus Middle	brain
50	chr6:29914400-29917200	Weak transcription	Dnd41	blood

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