Variant report

Variant	nsv601495
Chromosome Location	chr6:31237060-31242191
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:514)
CpG islands
(count:2811)
Chromatin interactive
region (count:5)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:514 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

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	BACH1	chr6:31239693-31240306	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr6:31239252-31239443	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr6:31241031-31241428	GM12878	blood:	n/a	n/a
6	BATF	chr6:31241012-31241391	GM12878	blood:	n/a	n/a
7	BCL11A	chr6:31241052-31241373	GM12878	blood:	n/a	n/a
8	BCL11A	chr6:31241100-31241317	GM12878	blood:	n/a	n/a
9	BCLAF1	chr6:31239341-31240264	GM12878	blood:	n/a	chr6:31240011-31240020
10	BCLAF1	chr6:31239585-31240141	GM12878	blood:	n/a	chr6:31240011-31240020
11	BHLHE40	chr6:31239789-31240109	HepG2	liver:	n/a	n/a
12	BHLHE40	chr6:31238745-31238982	GM12878	blood:	n/a	n/a
13	BHLHE40	chr6:31239841-31240041	K562	blood:	n/a	n/a
14	BHLHE40	chr6:31239743-31240181	GM12878	blood:	n/a	n/a
15	BRCA1	chr6:31239860-31240081	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr6:31239757-31239881	GM12878	blood:	n/a	n/a
17	CEBPB	chr6:31238263-31238458	IMR90	lung:	n/a	n/a
18	CEBPB	chr6:31240022-31240046	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr6:31238283-31238347	HepG2	liver:	n/a	n/a
20	CHD1	chr6:31239206-31240387	IMR90	lung:	n/a	n/a
21	CHD1	chr6:31239220-31240590	GM12878	blood:	n/a	n/a
22	CHD2	chr6:31239773-31240228	GM12878	blood:	n/a	n/a
23	CHD2	chr6:31239730-31240148	Hela-S3	cervix:	n/a	n/a
24	CHD2	chr6:31239823-31240131	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr6:31239932-31239957	K562	blood:	n/a	n/a
26	CHD2	chr6:31239741-31240088	HepG2	liver:	n/a	n/a
27	CREB1	chr6:31239689-31240116	H1-hESC	embryonic stem cell:	n/a	n/a
28	CREB1	chr6:31239648-31240296	GM12878	blood:	n/a	n/a
29	CREB1	chr6:31239714-31240134	ECC-1	luminal epithelium:	n/a	n/a
30	CREB1	chr6:31239170-31240252	GM12878	blood:	n/a	n/a
31	CREB1	chr6:31239737-31240264	K562	blood:	n/a	n/a
32	CREB1	chr6:31239704-31240161	ECC-1	luminal epithelium:	n/a	n/a
33	CREB1	chr6:31239786-31240124	A549	lung:	n/a	n/a
34	CREB1	chr6:31239283-31240185	HepG2	liver:	n/a	n/a
35	CREB1	chr6:31239703-31240235	HepG2	liver:	n/a	n/a
36	CREB1	chr6:31239402-31240117	A549	lung:	n/a	n/a
37	CREB1	chr6:31239705-31240198	K562	blood:	n/a	n/a
38	CREB1	chr6:31239669-31240189	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr6:31239440-31239590	GM06990	blood:	n/a	n/a
40	CTCF	chr6:31239440-31239590	HMEC	breast:	n/a	n/a
41	CTCF	chr6:31239580-31239730	AG09319	gingival:	n/a	n/a
42	CTCF	chr6:31239480-31239630	AG04450	lung:	n/a	n/a
43	CTCF	chr6:31239480-31239630	WERI-Rb-1	eye:	n/a	n/a
44	CTCF	chr6:31238874-31238948	GM13976	blood:	n/a	n/a
45	CTCF	chr6:31239420-31239570	SK-N-SH_RA	brain:	n/a	n/a
46	CTCF	chr6:31239420-31239570	BJ	skin:	n/a	n/a
47	CTCF	chr6:31239440-31239590	NHEK	skin:	n/a	n/a
48	CTCF	chr6:31239400-31239550	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr6:31239420-31239570	HRE	kidney:	n/a	n/a
50	CTCF	chr6:31239400-31239550	NHDF-neo	bronchial:	n/a	n/a

(count:2811 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:31238020-31238070	HMEC	breast:	n/a
2	chr6:31240651-31240701	HAEpiC	amniotic membrane:	n/a
3	chr6:31237034-31237084	MCF-7	breast:	n/a
4	chr6:31239916-31239966	HUVEC	blood vessel:	n/a
5	chr6:31237824-31237874	HL-60	blood:	n/a
6	chr6:31238020-31238070	HMEC	breast:	n/a
7	chr6:31240651-31240701	HAEpiC	amniotic membrane:	n/a
8	chr6:31237034-31237084	MCF-7	breast:	n/a
9	chr6:31239916-31239966	HUVEC	blood vessel:	n/a
10	chr6:31237824-31237874	HL-60	blood:	n/a
11	chr6:31239767-31239817	HL-60	blood:	n/a
12	chr6:31239653-31239703	GM19239	blood:	n/a
13	chr6:31241000-31241050	SK-N-MC	brain:	n/a
14	chr6:31239243-31239293	RPTEC	kidney:	n/a
15	chr6:31239093-31239143	MCF10A-Er-Src	breast:	n/a
16	chr6:31237013-31237063	SAEC	small airway:	n/a
17	chr6:31239411-31239461	GM06990	blood:	n/a
18	chr6:31237405-31237455	BE2_C	brain:	n/a
19	chr6:31239005-31239055	Hela-S3	cervix:	n/a
20	chr6:31240814-31240864	HCPEpiC	choroid plexus:	n/a
21	chr6:31238388-31238438	HIPEpiC	eye:	n/a
22	chr6:31239005-31239055	NHBE	bronchial:	n/a
23	chr6:31237405-31237455	T-47D	breast:	n/a
24	chr6:31239074-31239124	HAEpiC	amniotic membrane:	n/a
25	chr6:31238751-31238801	NH-A	brain:	n/a
26	chr6:31238751-31238801	HIPEpiC	eye:	n/a
27	chr6:31240651-31240701	H1-hESC	embryonic stem cell:	embryo
28	chr6:31240784-31240834	HUVEC	blood vessel:	n/a
29	chr6:31237405-31237455	ovcar-3	ovarian:	n/a
30	chr6:31239910-31239960	RPTEC	kidney:	n/a
31	chr6:31239247-31239297	HCPEpiC	choroid plexus:	n/a
32	chr6:31239402-31239452	U87	brain:	n/a
33	chr6:31237405-31237455	NHBE	bronchial:	n/a
34	chr6:31239259-31239309	T-47D	breast:	n/a
35	chr6:31238908-31238958	SKMC	muscle:	n/a
36	chr6:31238020-31238070	GM12891	blood:	n/a
37	chr6:31240050-31240100	GM12878	blood:	n/a
38	chr6:31237034-31237084	CMK	blood:	n/a
39	chr6:31237034-31237084	BE2_C	brain:	n/a
40	chr6:31238908-31238958	HepG2	liver:	n/a
41	chr6:31238036-31238086	MCF10A-Er-Src	breast:	n/a
42	chr6:31239133-31239183	IMR90	lung:	fetal
43	chr6:31241000-31241050	CMK	blood:	n/a
44	chr6:31237722-31237772	PFSK-1	brain:	n/a
45	chr6:31238751-31238801	GM12878	blood:	n/a
46	chr6:31237199-31237249	SK-N-SH_RA	brain:	n/a
47	chr6:31240223-31240273	HCT-116	colon:	n/a
48	chr6:31239324-31239374	AG04449	skin:	fetal
49	chr6:31237013-31237063	MCF-7	breast:	n/a
50	chr6:31239259-31239309	PANC-1	pancreas:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:29910138..29911769-chr6:31239456..31240978,2	MCF-7	breast:
2	chr6:31238976..31240351-chr6:31324393..31325523,6	HCT-116	colon:
3	chr6:31234807..31237311-chr6:31237898..31240961,3	K562	blood:
4	chr6:29855138..29856405-chr6:31238835..31239948,4	HCT-116	colon:
5	chr6:31238404..31240559-chr6:31321762..31324439,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HLA-C-2	chr6:31237115-31237443	NONHSAT108746

No data

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

Extended variants
information (count: 477 )
Associated
traits (count: 123 )

Variant overlapped rSNPs/rCNVs (count:477 , 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	rs180856400	chr6:31237060-31237061	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs2894204	chr6:31237061-31237062	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs371039627	chr6:31237085-31237086	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs17885557	chr6:31237087-31237088	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs375542879	chr6:31237104-31237105	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs1130838	chr6:31237124-31237125	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs35708511	chr6:31237162-31237163	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs545140350	chr6:31237193-31237194	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
9	rs542273765	chr6:31237199-31237200	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs281860589	chr6:31237200-31237201	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
11	rs370407485	chr6:31237208-31237209	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
12	rs527842025	chr6:31237217-31237218	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
13	rs185768419	chr6:31237229-31237230	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
14	rs9264596	chr6:31237230-31237231	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs9264597	chr6:31237233-31237234	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs17881458	chr6:31237237-31237238	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs550578214	chr6:31237250-31237251	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
18	rs41562921	chr6:31237254-31237255	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs386698956	chr6:31237255-31237256	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
20	rs41550315	chr6:31237264-31237265	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
21	rs111308207	chr6:31237268-31237269	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
22	rs3177824	chr6:31237269-31237270	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
23	rs139702282	chr6:31237272-31237273	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
24	rs41559915	chr6:31237275-31237276	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs76294545	chr6:31237284-31237285	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
26	rs568718965	chr6:31237289-31237290	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
27	rs567530604	chr6:31237312-31237313	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
28	rs68094471	chr6:31237323-31237324	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs66772001	chr6:31237333-31237334	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs72558163	chr6:31237342-31237343	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs386698957	chr6:31237353-31237354	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
32	rs543182678	chr6:31237380-31237381	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
33	rs56010430	chr6:31237405-31237406	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs386698958	chr6:31237437-31237438	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
35	rs68037221	chr6:31237449-31237450	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs72558161	chr6:31237457-31237458	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs386698959	chr6:31237461-31237462	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs66620546	chr6:31237463-31237464	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs72558159	chr6:31237513-31237514	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs200405836	chr6:31237528-31237529	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs45437892	chr6:31237542-31237543	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs3819287	chr6:31237563-31237564	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs537747274	chr6:31237565-31237566	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs72558157	chr6:31237571-31237572	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs529514818	chr6:31237576-31237577	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs372183108	chr6:31237578-31237579	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs373826500	chr6:31237584-31237585	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs9264606	chr6:31237592-31237593	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs9264607	chr6:31237605-31237606	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
50	rs189845311	chr6:31237659-31237660	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:123)

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
Melanoma	20877625	CNVD

Chromatin state (count:584 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31233200-31238200	Weak transcription	Stomach Mucosa	stomach
2	chr6:31233200-31238400	Weak transcription	Small Intestine	intestine
3	chr6:31234800-31237400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr6:31235000-31238600	Weak transcription	HSMM	muscle
5	chr6:31235200-31238400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr6:31235400-31237400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr6:31235400-31237800	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr6:31235600-31237200	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
9	chr6:31235600-31237200	Genic enhancers	Rectal Mucosa Donor 29	rectum
10	chr6:31235600-31237400	Strong transcription	Primary hematopoietic stem cells	blood
11	chr6:31235600-31237400	Strong transcription	Left Ventricle	heart
12	chr6:31235600-31238200	Strong transcription	H1 Cell Line	embryonic stem cell
13	chr6:31235600-31238400	Genic enhancers	Spleen	Spleen
14	chr6:31235600-31238400	Weak transcription	NH-A	brain
15	chr6:31235600-31238800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr6:31235600-31238800	Weak transcription	Fetal Kidney	kidney
17	chr6:31235800-31237200	Strong transcription	Placenta	Placenta
18	chr6:31235800-31237200	Strong transcription	Fetal Thymus	thymus
19	chr6:31235800-31237200	Strong transcription	Gastric	stomach
20	chr6:31235800-31237400	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr6:31235800-31237400	Strong transcription	Esophagus	oesophagus
22	chr6:31235800-31237600	Strong transcription	NHLF	lung
23	chr6:31235800-31238000	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr6:31235800-31238000	Genic enhancers	Primary B cells from peripheral blood	blood
25	chr6:31235800-31238200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr6:31235800-31238400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr6:31235800-31238400	Weak transcription	Cortex derived primary cultured neurospheres	brain
28	chr6:31235800-31238400	Weak transcription	Brain Substantia Nigra	brain
29	chr6:31235800-31238400	Strong transcription	Thymus	Thymus
30	chr6:31235800-31238600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr6:31235800-31238600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr6:31235800-31238600	Weak transcription	Fetal Lung	lung
33	chr6:31236000-31238200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr6:31236000-31238200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr6:31236000-31238200	Strong transcription	Fetal Muscle Leg	muscle
36	chr6:31236000-31238600	Strong transcription	Fetal Intestine Small	intestine
37	chr6:31236000-31238600	Weak transcription	HSMMtube	muscle
38	chr6:31236200-31237200	Strong transcription	Pancreas	Pancrea
39	chr6:31236200-31237400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
40	chr6:31236200-31237600	Strong transcription	Brain Anterior Caudate	brain
41	chr6:31236200-31237600	Strong transcription	Brain Hippocampus Middle	brain
42	chr6:31236200-31237600	Strong transcription	Lung	lung
43	chr6:31236200-31237800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
44	chr6:31236200-31237800	Strong transcription	Aorta	Aorta
45	chr6:31236200-31237800	Strong transcription	Placenta Amnion	Placenta Amnion
46	chr6:31236200-31238000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr6:31236200-31238400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
48	chr6:31236200-31238600	Strong transcription	H9 Cell Line	embryonic stem cell
49	chr6:31236200-31238600	Weak transcription	Brain Angular Gyrus	brain
50	chr6:31236200-31238800	Transcr. at gene 5' and 3'	Primary B cells from cord blood	blood

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