Variant report

Variant	nsv884029
Chromosome Location	chr6:29928649-29937924
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:966)
CpG islands
(count:549)
Chromatin interactive
region (count:21)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:966 , 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	chr6:29934522-29934914	K562	blood:	n/a	n/a
2	ARID3A	chr6:29932290-29932954	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:29932477-29933236	K562	blood:	n/a	n/a
4	ARID3A	chr6:29933775-29934240	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:29931139-29931164	K562	blood:	n/a	n/a
6	ARID3A	chr6:29935249-29935871	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:29933748-29934309	K562	blood:	n/a	n/a
8	ARID3A	chr6:29935252-29935904	K562	blood:	n/a	n/a
9	ARID3A	chr6:29937042-29937091	K562	blood:	n/a	n/a
10	ATF1	chr6:29935286-29935585	K562	blood:	n/a	n/a
11	ATF1	chr6:29932584-29933076	K562	blood:	n/a	n/a
12	ATF2	chr6:29932488-29932978	GM12878	blood:	n/a	n/a
13	ATF2	chr6:29932433-29933091	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	chr6:29932453-29933278	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr6:29932608-29933062	K562	blood:	n/a	n/a
18	BATF	chr6:29932589-29933017	GM12878	blood:	n/a	chr6:29932797-29932808 chr6:29932798-29932808
19	BATF	chr6:29932612-29932987	GM12878	blood:	n/a	chr6:29932797-29932808 chr6:29932798-29932808
20	BCL11A	chr6:29932602-29932969	GM12878	blood:	n/a	chr6:29932797-29932806
21	BCL11A	chr6:29932639-29932881	GM12878	blood:	n/a	chr6:29932797-29932806
22	BCL3	chr6:29932533-29932943	GM12878	blood:	n/a	chr6:29932797-29932806
23	BCLAF1	chr6:29932428-29933119	GM12878	blood:	n/a	chr6:29932797-29932806
24	BCLAF1	chr6:29932494-29933203	GM12878	blood:	n/a	chr6:29932797-29932806
25	BHLHE40	chr6:29932548-29933279	GM12878	blood:	n/a	n/a
26	BHLHE40	chr6:29933686-29934301	K562	blood:	n/a	n/a
27	BHLHE40	chr6:29935166-29935758	K562	blood:	n/a	n/a
28	BHLHE40	chr6:29932569-29933159	K562	blood:	n/a	n/a
29	BHLHE40	chr6:29933714-29934091	HepG2	liver:	n/a	n/a
30	BHLHE40	chr6:29933866-29934118	GM12878	blood:	n/a	n/a
31	BHLHE40	chr6:29934607-29934610	GM12878	blood:	n/a	n/a
32	CBX3	chr6:29932403-29933273	HCT-116	colon:	n/a	n/a
33	CBX3	chr6:29935109-29935665	K562	blood:	n/a	n/a
34	CBX3	chr6:29933685-29934511	HCT-116	colon:	n/a	n/a
35	CBX3	chr6:29935860-29936460	HCT-116	colon:	n/a	n/a
36	CBX3	chr6:29935905-29936437	HCT-116	colon:	n/a	n/a
37	CBX3	chr6:29932608-29932997	K562	blood:	n/a	n/a
38	CBX3	chr6:29932504-29933475	K562	blood:	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	chr6:29932426-29933189	K562	blood:	n/a	n/a
42	CEBPB	chr6:29935138-29935549	K562	blood:	n/a	chr6:29935249-29935260 chr6:29935210-29935221
43	CEBPB	chr6:29932451-29933116	GM12878	blood:	n/a	n/a
44	CEBPB	chr6:29934230-29934543	IMR90	lung:	n/a	n/a
45	CEBPB	chr6:29936002-29936359	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr6:29935064-29935418	HepG2	liver:	n/a	chr6:29935249-29935260 chr6:29935210-29935221
47	CEBPB	chr6:29929562-29929884	HepG2	liver:	n/a	n/a
48	CEBPB	chr6:29929504-29929848	K562	blood:	n/a	n/a
49	CEBPB	chr6:29932409-29933285	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr6:29932577-29933269	K562	blood:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:29933511-29933561	HPAEpiC	pulmonary alveolar:	n/a
2	chr6:29933915-29933965	Jurkat	blood:	n/a
3	chr6:29933697-29933747	HRE	kidney:	n/a
4	chr6:29933511-29933561	HNPCEpiC	eye:	n/a
5	chr6:29933697-29933747	BE2_C	brain:	n/a
6	chr6:29933915-29933965	SK-N-SH	brain:	n/a
7	chr6:29933411-29933461	HCF	heart:	n/a
8	chr6:29933697-29933747	GM19239	blood:	n/a
9	chr6:29933915-29933965	AG04449	skin:	fetal
10	chr6:29932743-29932793	PrEC	prostate:	n/a
11	chr6:29932743-29932793	HEEpiC	esophagus:	n/a
12	chr6:29933511-29933561	BE2_C	brain:	n/a
13	chr6:29933971-29934021	HPAEpiC	pulmonary alveolar:	n/a
14	chr6:29932864-29932914	HCF	heart:	n/a
15	chr6:29933915-29933965	HepG2	liver:	n/a
16	chr6:29932864-29932914	HCT-116	colon:	n/a
17	chr6:29932743-29932793	GM12878	blood:	n/a
18	chr6:29933915-29933965	Hela-S3	cervix:	n/a
19	chr6:29933915-29933965	HRCEpiC	kidney:	n/a
20	chr6:29933697-29933747	GM06990	blood:	n/a
21	chr6:29933411-29933461	A549	lung:	n/a
22	chr6:29933511-29933561	HMEC	breast:	n/a
23	chr6:29933511-29933561	GM12891	blood:	n/a
24	chr6:29932621-29932671	K562	blood:	n/a
25	chr6:29932621-29932671	HNPCEpiC	eye:	n/a
26	chr6:29933697-29933747	HIPEpiC	eye:	n/a
27	chr6:29933411-29933461	HIPEpiC	eye:	n/a
28	chr6:29932864-29932914	GM06990	blood:	n/a
29	chr6:29933697-29933747	IMR90	lung:	fetal
30	chr6:29932743-29932793	AG10803	skin:	n/a
31	chr6:29933511-29933561	HEK293	kidney:	embryo
32	chr6:29933925-29933975	CMK	blood:	n/a
33	chr6:29933697-29933747	SK-N-SH_RA	brain:	n/a
34	chr6:29933971-29934021	GM06990	blood:	n/a
35	chr6:29933915-29933965	PANC-1	pancreas:	n/a
36	chr6:29933411-29933461	HCPEpiC	choroid plexus:	n/a
37	chr6:29933411-29933461	HEEpiC	esophagus:	n/a
38	chr6:29933511-29933561	AoSMC	blood vessel:	n/a
39	chr6:29933511-29933561	ECC-1	luminal epithelium:	n/a
40	chr6:29933971-29934021	PrEC	prostate:	n/a
41	chr6:29933915-29933965	HEK293	kidney:	embryo
42	chr6:29933925-29933975	PrEC	prostate:	n/a
43	chr6:29933925-29933975	HRE	kidney:	n/a
44	chr6:29933915-29933965	PrEC	prostate:	n/a
45	chr6:29933915-29933965	AG04450	lung:	fetal
46	chr6:29933915-29933965	HPAEpiC	pulmonary alveolar:	n/a
47	chr6:29932621-29932671	NT2-D1	testis:	n/a
48	chr6:29933971-29934021	A549	lung:	n/a
49	chr6:29932864-29932914	ECC-1	luminal epithelium:	n/a
50	chr6:29933915-29933965	HAEpiC	amniotic membrane:	n/a

(count:21 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 513 )
Associated
traits (count: 112 )

Variant overlapped rSNPs/rCNVs (count:513 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2428521	chr6:29928649-29928650	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs373136863	chr6:29928675-29928676	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs377680302	chr6:29928678-29928679	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs200857754	chr6:29928694-29928695	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs2735081	chr6:29928698-29928699	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs2022671	chr6:29928706-29928707	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs200365423	chr6:29928722-29928723	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs149670107	chr6:29928756-29928757	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs377121643	chr6:29928788-29928789	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs531574636	chr6:29928796-29928797	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs17179957	chr6:29928815-29928816	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs112925679	chr6:29928823-29928824	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs2517692	chr6:29928826-29928827	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs2523935	chr6:29928838-29928839	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs368184481	chr6:29928841-29928842	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs375554154	chr6:29928871-29928872	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs146499308	chr6:29928879-29928880	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs17186356	chr6:29928881-29928882	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs147485588	chr6:29928932-29928933	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs199751627	chr6:29928996-29928997	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs200872159	chr6:29929005-29929006	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs201691243	chr6:29929012-29929013	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs6916499	chr6:29929038-29929039	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs186720925	chr6:29929039-29929040	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs142390188	chr6:29929043-29929044	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs2517691	chr6:29929055-29929056	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs2517690	chr6:29929073-29929074	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs560620962	chr6:29929079-29929080	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs17179978	chr6:29929095-29929096	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs75740175	chr6:29929109-29929110	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs563002136	chr6:29929123-29929124	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs17179985	chr6:29929144-29929145	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs116779968	chr6:29929147-29929148	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs561865514	chr6:29929149-29929150	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs17186370	chr6:29929174-29929175	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs9260705	chr6:29929191-29929192	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs6457104	chr6:29929227-29929228	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs539446852	chr6:29929236-29929237	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs2517689	chr6:29929253-29929254	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs9468668	chr6:29929264-29929265	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs115763149	chr6:29929275-29929276	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs17179992	chr6:29929324-29929325	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs9260706	chr6:29929336-29929337	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs527752966	chr6:29929354-29929355	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs17180006	chr6:29929360-29929361	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs140428734	chr6:29929437-29929438	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
47	rs17180013	chr6:29929444-29929445	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs191013349	chr6:29929445-29929446	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs567283658	chr6:29929473-29929474	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs556614016	chr6:29929489-29929490	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:642 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

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	chr6:29916800-29930000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
10	chr6:29916800-29932200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr6:29916800-29932200	Weak transcription	Rectal Mucosa Donor 31	rectum
12	chr6:29916800-29932200	Weak transcription	Sigmoid Colon	Sigmoid Colon
13	chr6:29916800-29933000	Weak transcription	Esophagus	oesophagus
14	chr6:29916800-29933000	Weak transcription	Pancreas	Pancrea
15	chr6:29916800-29933200	Weak transcription	Lung	lung
16	chr6:29916800-29940200	Weak transcription	Gastric	stomach
17	chr6:29917000-29931800	Weak transcription	Primary T helper cells fromperipheralblood	blood
18	chr6:29917200-29932000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
19	chr6:29917200-29932200	Weak transcription	Liver	Liver
20	chr6:29917200-29932200	Weak transcription	Brain Hippocampus Middle	brain
21	chr6:29917800-29932200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr6:29918000-29932000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
23	chr6:29918000-29932200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
24	chr6:29918000-29932200	Weak transcription	Fetal Intestine Small	intestine
25	chr6:29918200-29931800	Weak transcription	Primary T cells from cord blood	blood
26	chr6:29920400-29932200	Weak transcription	Duodenum Smooth Muscle	Duodenum
27	chr6:29921800-29929400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr6:29921800-29929600	Weak transcription	Psoas Muscle	Psoas
29	chr6:29921800-29932200	Weak transcription	Skeletal Muscle Male	skeletal muscle
30	chr6:29922000-29929600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr6:29924600-29932200	Weak transcription	Left Ventricle	heart
32	chr6:29924600-29932200	Weak transcription	Right Atrium	heart
33	chr6:29924800-29932200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr6:29924800-29933000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr6:29926000-29930600	Enhancers	Adipose Nuclei	Adipose
36	chr6:29926200-29929400	Weak transcription	K562	blood
37	chr6:29926200-29932600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr6:29926400-29931800	Weak transcription	Primary neutrophils fromperipheralblood	blood
39	chr6:29926400-29931800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
40	chr6:29927200-29931200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
41	chr6:29927400-29928800	Enhancers	Monocytes-CD14+_RO01746	blood
42	chr6:29927600-29930400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr6:29927800-29929600	Weak transcription	Primary monocytes fromperipheralblood	blood
44	chr6:29927800-29930400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr6:29927800-29931800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr6:29927800-29932000	Weak transcription	Primary B cells from cord blood	blood
47	chr6:29927800-29932000	Weak transcription	GM12878-XiMat	blood
48	chr6:29927800-29932200	Weak transcription	Primary B cells from peripheral blood	blood
49	chr6:29927800-29938800	Weak transcription	Spleen	Spleen
50	chr6:29928400-29928800	Weak transcription	HepG2	liver

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