Variant report

Variant	nsv884021
Chromosome Location	chr6:29926654-29937924
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:972)
CpG islands
(count:612)
Chromatin interactive
region (count:22)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:972 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:29931139-29931164	K562	blood:	n/a	n/a
2	ARID3A	chr6:29934522-29934914	K562	blood:	n/a	n/a
3	ARID3A	chr6:29932290-29932954	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:29933748-29934309	K562	blood:	n/a	n/a
5	ARID3A	chr6:29935252-29935904	K562	blood:	n/a	n/a
6	ARID3A	chr6:29932477-29933236	K562	blood:	n/a	n/a
7	ARID3A	chr6:29937042-29937091	K562	blood:	n/a	n/a
8	ARID3A	chr6:29935249-29935871	HepG2	liver:	n/a	n/a
9	ARID3A	chr6:29933775-29934240	HepG2	liver:	n/a	n/a
10	ATF1	chr6:29932584-29933076	K562	blood:	n/a	n/a
11	ATF1	chr6:29935286-29935585	K562	blood:	n/a	n/a
12	ATF2	chr6:29932433-29933091	GM12878	blood:	n/a	n/a
13	ATF2	chr6:29932488-29932978	GM12878	blood:	n/a	n/a
14	ATF3	chr6:29932615-29932943	K562	blood:	n/a	n/a
15	ATF3	chr6:29932539-29933023	K562	blood:	n/a	n/a
16	BACH1	chr6:29932608-29933062	K562	blood:	n/a	n/a
17	BACH1	chr6:29932453-29933278	H1-hESC	embryonic stem cell:	n/a	n/a
18	BATF	chr6:29932612-29932987	GM12878	blood:	n/a	chr6:29932797-29932808 chr6:29932798-29932808
19	BATF	chr6:29932589-29933017	GM12878	blood:	n/a	chr6:29932797-29932808 chr6:29932798-29932808
20	BCL11A	chr6:29932639-29932881	GM12878	blood:	n/a	chr6:29932797-29932806
21	BCL11A	chr6:29932602-29932969	GM12878	blood:	n/a	chr6:29932797-29932806
22	BCL3	chr6:29932533-29932943	GM12878	blood:	n/a	chr6:29932797-29932806
23	BCLAF1	chr6:29932494-29933203	GM12878	blood:	n/a	chr6:29932797-29932806
24	BCLAF1	chr6:29932428-29933119	GM12878	blood:	n/a	chr6:29932797-29932806
25	BHLHE40	chr6:29933686-29934301	K562	blood:	n/a	n/a
26	BHLHE40	chr6:29933714-29934091	HepG2	liver:	n/a	n/a
27	BHLHE40	chr6:29932548-29933279	GM12878	blood:	n/a	n/a
28	BHLHE40	chr6:29935166-29935758	K562	blood:	n/a	n/a
29	BHLHE40	chr6:29934607-29934610	GM12878	blood:	n/a	n/a
30	BHLHE40	chr6:29933866-29934118	GM12878	blood:	n/a	n/a
31	BHLHE40	chr6:29932569-29933159	K562	blood:	n/a	n/a
32	CBX3	chr6:29932403-29933273	HCT-116	colon:	n/a	n/a
33	CBX3	chr6:29932504-29933475	K562	blood:	n/a	n/a
34	CBX3	chr6:29935905-29936437	HCT-116	colon:	n/a	n/a
35	CBX3	chr6:29932608-29932997	K562	blood:	n/a	n/a
36	CBX3	chr6:29935860-29936460	HCT-116	colon:	n/a	n/a
37	CBX3	chr6:29935109-29935665	K562	blood:	n/a	n/a
38	CBX3	chr6:29933685-29934511	HCT-116	colon:	n/a	n/a
39	CCNT2	chr6:29935317-29935569	K562	blood:	n/a	n/a
40	CCNT2	chr6:29932623-29932970	K562	blood:	n/a	n/a
41	CEBPB	chr6:29935064-29935418	HepG2	liver:	n/a	chr6:29935249-29935260 chr6:29935210-29935221
42	CEBPB	chr6:29936002-29936359	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr6:29932451-29933116	GM12878	blood:	n/a	n/a
44	CEBPB	chr6:29929562-29929884	HepG2	liver:	n/a	n/a
45	CEBPB	chr6:29929504-29929848	K562	blood:	n/a	n/a
46	CEBPB	chr6:29932426-29933189	K562	blood:	n/a	n/a
47	CEBPB	chr6:29934230-29934543	IMR90	lung:	n/a	n/a
48	CEBPB	chr6:29932409-29933285	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr6:29935073-29935816	K562	blood:	n/a	chr6:29935249-29935260 chr6:29935210-29935221
50	CEBPB	chr6:29933654-29933956	HepG2	liver:	n/a	n/a

(count:612 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:29932621-29932671	Jurkat	blood:	n/a
2	chr6:29933511-29933561	SK-N-SH	brain:	n/a
3	chr6:29932621-29932671	Jurkat	blood:	n/a
4	chr6:29933511-29933561	SK-N-SH	brain:	n/a
5	chr6:29932621-29932671	HPAEpiC	pulmonary alveolar:	n/a
6	chr6:29932864-29932914	HUVEC	blood vessel:	n/a
7	chr6:29933915-29933965	IMR90	lung:	fetal
8	chr6:29933971-29934021	RPTEC	kidney:	n/a
9	chr6:29933411-29933461	ECC-1	luminal epithelium:	n/a
10	chr6:29933411-29933461	SK-N-MC	brain:	n/a
11	chr6:29928362-29928412	Hela-S3	cervix:	n/a
12	chr6:29933511-29933561	ovcar-3	ovarian:	n/a
13	chr6:29932621-29932671	PANC-1	pancreas:	n/a
14	chr6:29933971-29934021	NT2-D1	testis:	n/a
15	chr6:29933697-29933747	IMR90	lung:	fetal
16	chr6:29932743-29932793	T-47D	breast:	n/a
17	chr6:29928362-29928412	ovcar-3	ovarian:	n/a
18	chr6:29932743-29932793	HCPEpiC	choroid plexus:	n/a
19	chr6:29933925-29933975	HepG2	liver:	n/a
20	chr6:29933915-29933965	BE2_C	brain:	n/a
21	chr6:29933697-29933747	HepG2	liver:	n/a
22	chr6:29932621-29932671	A549	lung:	n/a
23	chr6:29932864-29932914	AG04449	skin:	fetal
24	chr6:29933697-29933747	AoSMC	blood vessel:	n/a
25	chr6:29932743-29932793	GM12892	blood:	n/a
26	chr6:29933411-29933461	GM19239	blood:	n/a
27	chr6:29933925-29933975	AG04450	lung:	fetal
28	chr6:29933511-29933561	GM06990	blood:	n/a
29	chr6:29933511-29933561	SK-N-SH_RA	brain:	n/a
30	chr6:29933511-29933561	HIPEpiC	eye:	n/a
31	chr6:29933697-29933747	HRPEpiC	eye:	n/a
32	chr6:29933511-29933561	PrEC	prostate:	n/a
33	chr6:29933411-29933461	AG04449	skin:	fetal
34	chr6:29933511-29933561	Caco-2	colon:	n/a
35	chr6:29933925-29933975	PrEC	prostate:	n/a
36	chr6:29933411-29933461	NHBE	bronchial:	n/a
37	chr6:29928362-29928412	CMK	blood:	n/a
38	chr6:29932864-29932914	HMEC	breast:	n/a
39	chr6:29932621-29932671	Caco-2	colon:	n/a
40	chr6:29933697-29933747	Jurkat	blood:	n/a
41	chr6:29932743-29932793	PFSK-1	brain:	n/a
42	chr6:29932621-29932671	GM12878	blood:	n/a
43	chr6:29933971-29934021	AG09319	gingival:	n/a
44	chr6:29933511-29933561	GM19239	blood:	n/a
45	chr6:29933915-29933965	HAEpiC	amniotic membrane:	n/a
46	chr6:29932743-29932793	Hepatocyte	liver:	n/a
47	chr6:29933511-29933561	PFSK-1	brain:	n/a
48	chr6:29928362-29928412	AG09309	skin:	n/a
49	chr6:29933411-29933461	HepG2	liver:	n/a
50	chr6:29932621-29932671	HCT-116	colon:	n/a

(count:22 , 50 per page) page: 1

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

No data

Variant related genes	Relation type
HCG9	TF binding region
HCG9	CpG island
ENSG00000230795	chromatin interactions
ENSG00000204619	chromatin interactions
ENSG00000259081	chromatin interactions
ENSG00000204625	chromatin interactions
ENSG00000204623	chromatin interactions
ENSG00000066379	chromatin interactions

Extended variants
information (count: 619 )
Associated
traits (count: 112 )

Variant overlapped rSNPs/rCNVs (count:619 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9260684	chr6:29926654-29926655	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs9260685	chr6:29926668-29926669	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs192872777	chr6:29926684-29926685	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs9260686	chr6:29926696-29926697	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs552014129	chr6:29926750-29926751	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs184999106	chr6:29926755-29926756	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs537451191	chr6:29926758-29926759	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs529735643	chr6:29926759-29926760	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs557074665	chr6:29926760-29926761	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs538991794	chr6:29926761-29926762	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs2517698	chr6:29926832-29926833	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs547809964	chr6:29926834-29926835	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs370715422	chr6:29926857-29926858	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs552763197	chr6:29926867-29926868	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs199556257	chr6:29926893-29926894	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs374415661	chr6:29926906-29926907	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs368576034	chr6:29926934-29926935	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs2523939	chr6:29926940-29926941	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs2517697	chr6:29926951-29926952	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs2523938	chr6:29926976-29926977	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs114696389	chr6:29927013-29927014	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs114905642	chr6:29927014-29927015	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
23	rs369795850	chr6:29927024-29927025	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs368486625	chr6:29927050-29927051	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs112549520	chr6:29927057-29927058	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs559997872	chr6:29927068-29927069	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs138083754	chr6:29927094-29927095	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs2735085	chr6:29927095-29927096	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs571902795	chr6:29927139-29927140	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs2394246	chr6:29927168-29927169	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs2523937	chr6:29927221-29927222	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs567285816	chr6:29927274-29927275	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs114577328	chr6:29927282-29927283	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs2571398	chr6:29927303-29927304	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs544722407	chr6:29927307-29927308	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs12529094	chr6:29927331-29927332	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs200756775	chr6:29927393-29927394	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs572997912	chr6:29927406-29927407	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs201927050	chr6:29927417-29927418	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs112992829	chr6:29927420-29927421	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs201371481	chr6:29927422-29927423	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs2735083	chr6:29927463-29927464	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs187971242	chr6:29927491-29927492	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs377532318	chr6:29927523-29927524	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs9260693	chr6:29927534-29927535	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs560885079	chr6:29927599-29927600	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs386698628	chr6:29927610-29927611	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs2517696	chr6:29927611-29927612	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs2517695	chr6:29927629-29927630	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs375780843	chr6:29927712-29927713	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:112)

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

Chromatin state (count:666 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:29913400-29932200	Weak transcription	Brain Anterior Caudate	brain
2	chr6:29913400-29932600	Weak transcription	Brain Substantia Nigra	brain
3	chr6:29913800-29932200	Weak transcription	Small Intestine	intestine
4	chr6:29914000-29932200	Weak transcription	Colon Smooth Muscle	Colon
5	chr6:29914600-29932200	Weak transcription	Colonic Mucosa	Colon
6	chr6:29914800-29932200	Weak transcription	Right Ventricle	heart
7	chr6:29915400-29931800	Weak transcription	Fetal Thymus	thymus
8	chr6:29915600-29932000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
9	chr6:29916800-29928200	Weak transcription	HepG2	liver
10	chr6:29916800-29930000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
11	chr6:29916800-29932200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr6:29916800-29932200	Weak transcription	Rectal Mucosa Donor 31	rectum
13	chr6:29916800-29932200	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr6:29916800-29933000	Weak transcription	Esophagus	oesophagus
15	chr6:29916800-29933000	Weak transcription	Pancreas	Pancrea
16	chr6:29916800-29933200	Weak transcription	Lung	lung
17	chr6:29916800-29940200	Weak transcription	Gastric	stomach
18	chr6:29917000-29926800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
19	chr6:29917000-29931800	Weak transcription	Primary T helper cells fromperipheralblood	blood
20	chr6:29917200-29932000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
21	chr6:29917200-29932200	Weak transcription	Liver	Liver
22	chr6:29917200-29932200	Weak transcription	Brain Hippocampus Middle	brain
23	chr6:29917400-29927400	Weak transcription	Fetal Muscle Leg	muscle
24	chr6:29917800-29932200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
25	chr6:29918000-29932000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
26	chr6:29918000-29932200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
27	chr6:29918000-29932200	Weak transcription	Fetal Intestine Small	intestine
28	chr6:29918200-29931800	Weak transcription	Primary T cells from cord blood	blood
29	chr6:29918400-29927400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
30	chr6:29919000-29926800	Weak transcription	Primary B cells from cord blood	blood
31	chr6:29920400-29932200	Weak transcription	Duodenum Smooth Muscle	Duodenum
32	chr6:29921800-29929400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr6:29921800-29929600	Weak transcription	Psoas Muscle	Psoas
34	chr6:29921800-29932200	Weak transcription	Skeletal Muscle Male	skeletal muscle
35	chr6:29922000-29929600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr6:29922400-29927600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr6:29924600-29932200	Weak transcription	Left Ventricle	heart
38	chr6:29924600-29932200	Weak transcription	Right Atrium	heart
39	chr6:29924800-29932200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr6:29924800-29933000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr6:29926000-29927000	Enhancers	Monocytes-CD14+_RO01746	blood
42	chr6:29926000-29927200	Enhancers	Spleen	Spleen
43	chr6:29926000-29930600	Enhancers	Adipose Nuclei	Adipose
44	chr6:29926200-29929400	Weak transcription	K562	blood
45	chr6:29926200-29932600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr6:29926400-29927800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr6:29926400-29927800	Enhancers	GM12878-XiMat	blood
48	chr6:29926400-29931800	Weak transcription	Primary neutrophils fromperipheralblood	blood
49	chr6:29926400-29931800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
50	chr6:29926600-29926800	Enhancers	Skeletal Muscle Female	skeletal muscle

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