Variant report

Variant	esv3398089
Chromosome Location	chr6:31235473-31240071
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:559)
CpG islands
(count:2507)
Chromatin interactive
region (count:8)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:559 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr6:31239808-31240131	K562	blood:	n/a	n/a
2	ATF2	chr6:31239651-31240115	GM12878	blood:	n/a	n/a
3	ATF2	chr6:31235265-31236206	GM12878	blood:	n/a	n/a
4	ATF2	chr6:31235142-31236449	GM12878	blood:	n/a	n/a
5	BACH1	chr6:31239252-31239443	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr6:31239693-31240306	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL11A	chr6:31234485-31235770	GM12878	blood:	n/a	n/a
8	BCL3	chr6:31235264-31235791	GM12878	blood:	n/a	n/a
9	BCL3	chr6:31235297-31235807	GM12878	blood:	n/a	n/a
10	BCLAF1	chr6:31239341-31240264	GM12878	blood:	n/a	chr6:31240011-31240020
11	BCLAF1	chr6:31235169-31236336	GM12878	blood:	n/a	n/a
12	BCLAF1	chr6:31239585-31240141	GM12878	blood:	n/a	chr6:31240011-31240020
13	BCLAF1	chr6:31235268-31236420	GM12878	blood:	n/a	n/a
14	BHLHE40	chr6:31239841-31240041	K562	blood:	n/a	n/a
15	BHLHE40	chr6:31238745-31238982	GM12878	blood:	n/a	n/a
16	BHLHE40	chr6:31239743-31240181	GM12878	blood:	n/a	n/a
17	BHLHE40	chr6:31239789-31240109	HepG2	liver:	n/a	n/a
18	BRCA1	chr6:31239860-31240081	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr6:31239757-31239881	GM12878	blood:	n/a	n/a
20	CEBPB	chr6:31240022-31240046	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr6:31238283-31238347	HepG2	liver:	n/a	n/a
22	CEBPB	chr6:31238263-31238458	IMR90	lung:	n/a	n/a
23	CHD1	chr6:31239206-31240387	IMR90	lung:	n/a	n/a
24	CHD1	chr6:31239220-31240590	GM12878	blood:	n/a	n/a
25	CHD2	chr6:31235463-31235965	GM12878	blood:	n/a	n/a
26	CHD2	chr6:31239730-31240148	Hela-S3	cervix:	n/a	n/a
27	CHD2	chr6:31239773-31240228	GM12878	blood:	n/a	n/a
28	CHD2	chr6:31239823-31240131	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr6:31236281-31236435	GM12878	blood:	n/a	n/a
30	CHD2	chr6:31239932-31239957	K562	blood:	n/a	n/a
31	CHD2	chr6:31239741-31240088	HepG2	liver:	n/a	n/a
32	CREB1	chr6:31239170-31240252	GM12878	blood:	n/a	n/a
33	CREB1	chr6:31239648-31240296	GM12878	blood:	n/a	n/a
34	CREB1	chr6:31239786-31240124	A549	lung:	n/a	n/a
35	CREB1	chr6:31239402-31240117	A549	lung:	n/a	n/a
36	CREB1	chr6:31239669-31240189	H1-hESC	embryonic stem cell:	n/a	n/a
37	CREB1	chr6:31239704-31240161	ECC-1	luminal epithelium:	n/a	n/a
38	CREB1	chr6:31239689-31240116	H1-hESC	embryonic stem cell:	n/a	n/a
39	CREB1	chr6:31239714-31240134	ECC-1	luminal epithelium:	n/a	n/a
40	CREB1	chr6:31239283-31240185	HepG2	liver:	n/a	n/a
41	CREB1	chr6:31239737-31240264	K562	blood:	n/a	n/a
42	CREB1	chr6:31239703-31240235	HepG2	liver:	n/a	n/a
43	CREB1	chr6:31239705-31240198	K562	blood:	n/a	n/a
44	CTCF	chr6:31239424-31239601	LNCaP	prostate:	n/a	n/a
45	CTCF	chr6:31239458-31239592	Lung_OC	lung:	n/a	n/a
46	CTCF	chr6:31239420-31239570	AoAF	blood vessel:	n/a	n/a
47	CTCF	chr6:31239400-31239550	A549	lung:	n/a	n/a
48	CTCF	chr6:31239395-31239668	K562	blood:	n/a	n/a
49	CTCF	chr6:31239442-31239594	GM19238	blood:	n/a	n/a
50	CTCF	chr6:31239380-31239530	HAc	cerebellar:	n/a	n/a

(count:2507 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:31239063-31239113	HCT-116	colon:	n/a
2	chr6:31239247-31239297	HCPEpiC	choroid plexus:	n/a
3	chr6:31239158-31239208	HL-60	blood:	n/a
4	chr6:31239295-31239345	AoSMC	blood vessel:	n/a
5	chr6:31237722-31237772	NHBE	bronchial:	n/a
6	chr6:31239005-31239055	AG04450	lung:	fetal
7	chr6:31239063-31239113	HCT-116	colon:	n/a
8	chr6:31239247-31239297	HCPEpiC	choroid plexus:	n/a
9	chr6:31239158-31239208	HL-60	blood:	n/a
10	chr6:31239295-31239345	AoSMC	blood vessel:	n/a
11	chr6:31237722-31237772	NHBE	bronchial:	n/a
12	chr6:31239005-31239055	AG04450	lung:	fetal
13	chr6:31239074-31239124	GM06990	blood:	n/a
14	chr6:31237029-31237079	NHBE	bronchial:	n/a
15	chr6:31239175-31239225	T-47D	breast:	n/a
16	chr6:31239916-31239966	PrEC	prostate:	n/a
17	chr6:31239243-31239293	ovcar-3	ovarian:	n/a
18	chr6:31237405-31237455	Jurkat	blood:	n/a
19	chr6:31238388-31238438	GM06990	blood:	n/a
20	chr6:31239243-31239293	HL-60	blood:	n/a
21	chr6:31239063-31239113	K562	blood:	n/a
22	chr6:31239093-31239143	GM12891	blood:	n/a
23	chr6:31237405-31237455	AG04450	lung:	fetal
24	chr6:31240050-31240100	GM12892	blood:	n/a
25	chr6:31238908-31238958	GM12892	blood:	n/a
26	chr6:31237013-31237063	HL-60	blood:	n/a
27	chr6:31238245-31238295	HEK293	kidney:	embryo
28	chr6:31239295-31239345	HL-60	blood:	n/a
29	chr6:31239175-31239225	K562	blood:	n/a
30	chr6:31239175-31239225	HEK293	kidney:	embryo
31	chr6:31239320-31239370	AG04450	lung:	fetal
32	chr6:31238388-31238438	HepG2	liver:	n/a
33	chr6:31239295-31239345	HNPCEpiC	eye:	n/a
34	chr6:31239320-31239370	HUVEC	blood vessel:	n/a
35	chr6:31238788-31238838	AG09319	gingival:	n/a
36	chr6:31237722-31237772	GM12891	blood:	n/a
37	chr6:31238036-31238086	SKMC	muscle:	n/a
38	chr6:31239063-31239113	NB4	blood:	n/a
39	chr6:31240045-31240095	HCPEpiC	choroid plexus:	n/a
40	chr6:31238267-31238317	GM06990	blood:	n/a
41	chr6:31238267-31238317	H1-hESC	embryonic stem cell:	embryo
42	chr6:31238788-31238838	SKMC	muscle:	n/a
43	chr6:31238267-31238317	AG09319	gingival:	n/a
44	chr6:31237199-31237249	GM12892	blood:	n/a
45	chr6:31238803-31238853	SAEC	small airway:	n/a
46	chr6:31239916-31239966	SKMC	muscle:	n/a
47	chr6:31239175-31239225	HAEpiC	amniotic membrane:	n/a
48	chr6:31237029-31237079	HCT-116	colon:	n/a
49	chr6:31237824-31237874	GM12878	blood:	n/a
50	chr6:31239320-31239370	SK-N-MC	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr6:31235298..31236799-chr6:31321704..31323597,2	K562	blood:
2	chr6:31238404..31240559-chr6:31321762..31324439,3	MCF-7	breast:
3	chr6:31176797..31178729-chr6:31234671..31236847,2	K562	blood:
4	chr6:31233619..31236964-chr6:31319655..31321766,4	MCF-7	breast:
5	chr6:29910138..29911769-chr6:31239456..31240978,2	MCF-7	breast:
6	chr6:31234807..31237311-chr6:31237898..31240961,3	K562	blood:
7	chr6:31238976..31240351-chr6:31324393..31325523,6	HCT-116	colon:
8	chr6:29855138..29856405-chr6:31238835..31239948,4	HCT-116	colon:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HLA-C-2	chr6:31236531-31236950	NONHSAT108747
2	lnc-HLA-C-2	chr6:31237115-31237443	NONHSAT108746
3	lnc-HLA-C-2	chr6:31236526-31236950	NONHSAT108746

No data

Variant related genes	Relation type
USP8P1	TF binding region
HLA-C	TF binding region
USP8P1	CpG island
HLA-C	CpG island
ENSG00000271581	chromatin interactions
ENSG00000206503	chromatin interactions
ENSG00000230521	chromatin interactions
ENSG00000204525	chromatin interactions
ENSG00000206341	chromatin interactions
ENSG00000234745	chromatin interactions
ENSG00000227766	chromatin interactions

Extended variants
information (count: 491 )
Associated
traits (count: 122 )

Variant overlapped rSNPs/rCNVs (count:491 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9368668	chr6:31235480-31235481	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs368312448	chr6:31235498-31235499	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs562401338	chr6:31235499-31235500	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs386698949	chr6:31235500-31235501	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs571022361	chr6:31235502-31235503	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs2853953	chr6:31235505-31235506	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs114938181	chr6:31235510-31235511	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs576474460	chr6:31235521-31235522	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs59286348	chr6:31235526-31235527	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs143394362	chr6:31235530-31235531	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs371536045	chr6:31235550-31235551	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs541786803	chr6:31235552-31235553	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs6907910	chr6:31235558-31235559	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs9264575	chr6:31235576-31235577	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs2524101	chr6:31235598-31235599	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs190533253	chr6:31235605-31235606	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs6907622	chr6:31235610-31235611	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs549546966	chr6:31235621-31235622	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs9380231	chr6:31235632-31235633	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs538541156	chr6:31235639-31235640	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs547239160	chr6:31235648-31235649	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs565845209	chr6:31235653-31235654	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs76235944	chr6:31235662-31235663	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs200079831	chr6:31235671-31235672	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs537578494	chr6:31235705-31235706	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs9264578	chr6:31235708-31235709	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs9264579	chr6:31235746-31235747	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs10807087	chr6:31235751-31235752	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs2524100	chr6:31235769-31235770	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs113792081	chr6:31235775-31235776	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs112707938	chr6:31235782-31235783	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs9264581	chr6:31235786-31235787	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs373739916	chr6:31235805-31235806	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs9264582	chr6:31235816-31235817	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs564639093	chr6:31235817-31235818	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs147179300	chr6:31235847-31235848	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs547204503	chr6:31235853-31235854	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs573644521	chr6:31235858-31235859	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs565935081	chr6:31235868-31235869	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs2853952	chr6:31235869-31235870	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs548549119	chr6:31235939-31235940	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs182732985	chr6:31235950-31235951	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs569993446	chr6:31235953-31235954	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs185648438	chr6:31235955-31235956	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs59672958	chr6:31235956-31235957	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs535198512	chr6:31235962-31235963	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs553313994	chr6:31235963-31235964	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs556547934	chr6:31235996-31235997	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs386698950	chr6:31236034-31236035	Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs115042889	chr6:31236035-31236036	Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:122)

Disease	PMID	Source
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
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	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
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21785460	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	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
abnormal development	18461090	CNVD
Melanoma	17363583	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
Breast cancer	21364760	CNVD
Systemic lupus erythematosus	19279649	CNVD
Retinoblastoma	16790693	CNVD
Acute myocardial infarction	18032375	CNVD
Renal cell carcinoma	19150565	CNVD
Systemic lupus erythematosus	19591781	CNVD
Attention deficit hyperactivity disorder	19287146	CNVD
Autism	19287146	CNVD
Erythema nodosum in leprosy	19287146	CNVD
Henoch-schoenlein purpura	19287146	CNVD
Liver cirrhosis	19287146	CNVD
Systemic lupus erythematosus	19287146	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	CNVD
Osteosarcoma	16790693	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
lymphocytic leukemia	21291569	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:575 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31228200-31235800	Weak transcription	Fetal Thymus	thymus
2	chr6:31230200-31235600	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr6:31231800-31235600	Weak transcription	Left Ventricle	heart
4	chr6:31232600-31235600	Weak transcription	Primary hematopoietic stem cells	blood
5	chr6:31232600-31236800	Weak transcription	Skeletal Muscle Male	skeletal muscle
6	chr6:31232800-31235600	Weak transcription	Colonic Mucosa	Colon
7	chr6:31232800-31235800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr6:31233200-31235600	Weak transcription	Liver	Liver
9	chr6:31233200-31235800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr6:31233200-31235800	Weak transcription	Placenta	Placenta
11	chr6:31233200-31236000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr6:31233200-31236600	Weak transcription	HMEC	breast
13	chr6:31233200-31238200	Weak transcription	Stomach Mucosa	stomach
14	chr6:31233200-31238400	Weak transcription	Small Intestine	intestine
15	chr6:31233400-31235600	Weak transcription	Monocytes-CD14+_RO01746	blood
16	chr6:31233400-31235800	Weak transcription	Primary monocytes fromperipheralblood	blood
17	chr6:31233400-31235800	Weak transcription	Adipose Nuclei	Adipose
18	chr6:31233400-31235800	Weak transcription	GM12878-XiMat	blood
19	chr6:31233400-31236200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
20	chr6:31233600-31235800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr6:31233600-31236400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr6:31233800-31236000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr6:31233800-31236400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
24	chr6:31233800-31236600	Weak transcription	Duodenum Smooth Muscle	Duodenum
25	chr6:31233800-31236800	Weak transcription	Stomach Smooth Muscle	stomach
26	chr6:31234000-31235600	Weak transcription	Skeletal Muscle Female	skeletal muscle
27	chr6:31234000-31235800	Weak transcription	Esophagus	oesophagus
28	chr6:31234000-31235800	Weak transcription	Gastric	stomach
29	chr6:31234000-31236000	Weak transcription	Primary B cells from cord blood	blood
30	chr6:31234000-31236200	Weak transcription	Aorta	Aorta
31	chr6:31234000-31236800	Weak transcription	Rectal Smooth Muscle	rectum
32	chr6:31234000-31237000	Weak transcription	Colon Smooth Muscle	Colon
33	chr6:31234200-31235800	Weak transcription	Thymus	Thymus
34	chr6:31234200-31236200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr6:31234200-31236600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr6:31234200-31236600	Weak transcription	Osteobl	bone
37	chr6:31234400-31236200	Weak transcription	Placenta Amnion	Placenta Amnion
38	chr6:31234400-31236400	Weak transcription	HUES6 Cell Line	embryonic stem cell
39	chr6:31234400-31236800	Weak transcription	HUES64 Cell Line	embryonic stem cell
40	chr6:31234400-31237000	Weak transcription	Ovary	ovary
41	chr6:31234600-31235600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
42	chr6:31234600-31235600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
43	chr6:31234600-31235800	Enhancers	Primary B cells from peripheral blood	blood
44	chr6:31234600-31236200	Weak transcription	H9 Cell Line	embryonic stem cell
45	chr6:31234600-31236200	Weak transcription	Brain Anterior Caudate	brain
46	chr6:31234600-31236200	Weak transcription	Brain Hippocampus Middle	brain
47	chr6:31234600-31236200	Weak transcription	Lung	lung
48	chr6:31234600-31236400	Weak transcription	HUES48 Cell Line	embryonic stem cell
49	chr6:31234600-31236800	Weak transcription	Dnd41	blood
50	chr6:31234800-31235800	Enhancers	Primary T helper naive cells from peripheral blood	blood

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