Variant report

Variant	esv1849702
Chromosome Location	chr8:110594148-110683804
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2180)
CpG islands
(count:1222)
Chromatin interactive
region (count:156)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2180 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:110664704-110664962	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:110651843-110653048	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:110619901-110620440	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:110605197-110606300	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:110619181-110619521	HepG2	liver:	n/a	n/a
6	ARID3A	chr8:110678575-110678618	K562	blood:	n/a	n/a
7	ARID3A	chr8:110596356-110596975	HepG2	liver:	n/a	n/a
8	ARID3A	chr8:110656368-110656623	HepG2	liver:	n/a	n/a
9	ARID3A	chr8:110655021-110655482	K562	blood:	n/a	n/a
10	ARID3A	chr8:110657512-110658350	HepG2	liver:	n/a	n/a
11	ARID3A	chr8:110656860-110657076	HepG2	liver:	n/a	n/a
12	ATF1	chr8:110654872-110655594	K562	blood:	n/a	n/a
13	ATF2	chr8:110604419-110605051	GM12878	blood:	n/a	n/a
14	ATF2	chr8:110608002-110608513	GM12878	blood:	n/a	n/a
15	ATF2	chr8:110607810-110608520	GM12878	blood:	n/a	n/a
16	ATF2	chr8:110604470-110605159	GM12878	blood:	n/a	n/a
17	ATF2	chr8:110606443-110607348	GM12878	blood:	n/a	n/a
18	ATF3	chr8:110605681-110606214	A549	lung:	n/a	n/a
19	ATF3	chr8:110656815-110657225	K562	blood:	n/a	chr8:110657073-110657082 chr8:110656979-110656988
20	BACH1	chr8:110656564-110657255	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr8:110597531-110597683	K562	blood:	n/a	n/a
22	BCL11A	chr8:110604550-110604974	GM12878	blood:	n/a	chr8:110604931-110604940
23	BCL11A	chr8:110619528-110619862	GM12878	blood:	n/a	n/a
24	BCL11A	chr8:110619515-110619837	GM12878	blood:	n/a	n/a
25	BCLAF1	chr8:110604470-110605155	GM12878	blood:	n/a	chr8:110604931-110604940
26	BCLAF1	chr8:110604502-110605022	GM12878	blood:	n/a	chr8:110604931-110604940
27	BHLHE40	chr8:110656066-110656188	K562	blood:	n/a	n/a
28	BHLHE40	chr8:110650339-110650672	HepG2	liver:	n/a	n/a
29	BHLHE40	chr8:110656875-110657220	GM12878	blood:	n/a	chr8:110656916-110656932 chr8:110656977-110656993 chr8:110657171-110657187 chr8:110657023-110657039 chr8:110656985-110657001
30	BHLHE40	chr8:110656874-110657631	K562	blood:	n/a	chr8:110656916-110656932 chr8:110656977-110656993 chr8:110657171-110657187 chr8:110657023-110657039 chr8:110656985-110657001
31	BHLHE40	chr8:110654773-110655271	GM12878	blood:	n/a	n/a
32	BHLHE40	chr8:110605586-110606212	HepG2	liver:	n/a	n/a
33	BHLHE40	chr8:110619982-110620472	HepG2	liver:	n/a	n/a
34	BHLHE40	chr8:110656581-110657315	HepG2	liver:	n/a	chr8:110656916-110656932 chr8:110656977-110656993 chr8:110657171-110657187 chr8:110657023-110657039 chr8:110656985-110657001
35	BHLHE40	chr8:110604564-110605005	GM12878	blood:	n/a	n/a
36	BHLHE40	chr8:110652702-110652907	HepG2	liver:	n/a	n/a
37	BHLHE40	chr8:110654773-110655762	K562	blood:	n/a	n/a
38	BRCA1	chr8:110664745-110664945	H1-hESC	embryonic stem cell:	n/a	n/a
39	BRCA1	chr8:110657930-110658121	H1-hESC	embryonic stem cell:	n/a	n/a
40	BRCA1	chr8:110657387-110657556	HepG2	liver:	n/a	n/a
41	BRCA1	chr8:110656051-110657237	Hela-S3	cervix:	n/a	n/a
42	CBX3	chr8:110656759-110657446	K562	blood:	n/a	n/a
43	CBX3	chr8:110618740-110620595	HCT-116	colon:	n/a	n/a
44	CBX3	chr8:110654774-110655126	K562	blood:	n/a	n/a
45	CBX3	chr8:110632672-110634114	HCT-116	colon:	n/a	n/a
46	CBX3	chr8:110618708-110620616	HCT-116	colon:	n/a	n/a
47	CBX3	chr8:110605596-110607241	HCT-116	colon:	n/a	n/a
48	CCNT2	chr8:110656764-110657381	K562	blood:	n/a	n/a
49	CCNT2	chr8:110623489-110623738	K562	blood:	n/a	n/a
50	CEBPB	chr8:110655994-110656374	HepG2	liver:	n/a	chr8:110656169-110656180

(count:1222 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:110661735-110661785	AG09319	gingival:	n/a
2	chr8:110657197-110657247	SAEC	small airway:	n/a
3	chr8:110661735-110661785	AG09319	gingival:	n/a
4	chr8:110657197-110657247	SAEC	small airway:	n/a
5	chr8:110656166-110656216	GM12891	blood:	n/a
6	chr8:110657854-110657904	K562	blood:	n/a
7	chr8:110658029-110658079	HCPEpiC	choroid plexus:	n/a
8	chr8:110656982-110657032	GM19239	blood:	n/a
9	chr8:110656442-110656492	MCF10A-Er-Src	breast:	n/a
10	chr8:110657193-110657243	MCF-7	breast:	n/a
11	chr8:110657182-110657232	AG09309	skin:	n/a
12	chr8:110657182-110657232	GM06990	blood:	n/a
13	chr8:110657174-110657224	HRE	kidney:	n/a
14	chr8:110656096-110656146	SK-N-MC	brain:	n/a
15	chr8:110608037-110608087	Jurkat	blood:	n/a
16	chr8:110657174-110657224	SAEC	small airway:	n/a
17	chr8:110657193-110657243	RPTEC	kidney:	n/a
18	chr8:110661735-110661785	GM12878	blood:	n/a
19	chr8:110657193-110657243	NHDF-neo	bronchial:	n/a
20	chr8:110657539-110657589	AG04449	skin:	fetal
21	chr8:110657539-110657589	BE2_C	brain:	n/a
22	chr8:110656245-110656295	Hela-S3	cervix:	n/a
23	chr8:110657197-110657247	U87	brain:	n/a
24	chr8:110657184-110657234	AG09319	gingival:	n/a
25	chr8:110656166-110656216	NT2-D1	testis:	n/a
26	chr8:110656982-110657032	GM12891	blood:	n/a
27	chr8:110661013-110661063	PrEC	prostate:	n/a
28	chr8:110657197-110657247	BE2_C	brain:	n/a
29	chr8:110658029-110658079	HCM	heart:	n/a
30	chr8:110657184-110657234	GM12892	blood:	n/a
31	chr8:110608037-110608087	Hepatocyte	liver:	n/a
32	chr8:110657197-110657247	GM12892	blood:	n/a
33	chr8:110658029-110658079	U87	brain:	n/a
34	chr8:110656982-110657032	AoSMC	blood vessel:	n/a
35	chr8:110659094-110659144	HepG2	liver:	n/a
36	chr8:110657854-110657904	GM12892	blood:	n/a
37	chr8:110656442-110656492	SK-N-SH	brain:	n/a
38	chr8:110661735-110661785	HMEC	breast:	n/a
39	chr8:110657854-110657904	PANC-1	pancreas:	n/a
40	chr8:110661735-110661785	SK-N-SH_RA	brain:	n/a
41	chr8:110656245-110656295	MCF10A-Er-Src	breast:	n/a
42	chr8:110661013-110661063	H1-hESC	embryonic stem cell:	embryo
43	chr8:110656394-110656444	HCM	heart:	n/a
44	chr8:110657193-110657243	SAEC	small airway:	n/a
45	chr8:110657184-110657234	SK-N-SH_RA	brain:	n/a
46	chr8:110657193-110657243	PANC-1	pancreas:	n/a
47	chr8:110657877-110657927	NH-A	brain:	n/a
48	chr8:110657877-110657927	HNPCEpiC	eye:	n/a
49	chr8:110657174-110657224	AG09309	skin:	n/a
50	chr8:110656245-110656295	HL-60	blood:	n/a

(count:156 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr8:110623120..110625738-chr8:110638135..110640971,2	K562	blood:
2	chr8:110656684..110658658-chr8:110660535..110663260,4	MCF-7	breast:
3	chr8:110551172..110552900-chr8:110613869..110616553,2	MCF-7	breast:
4	chr8:110643544..110645348-chr8:110650716..110653682,2	MCF-7	breast:
5	chr8:110344753..110346999-chr8:110656055..110658588,2	MCF-7	breast:
6	chr8:110595213..110597176-chr8:110600323..110601967,2	MCF-7	breast:
7	chr8:110612107..110614990-chr8:110621772..110623731,2	MCF-7	breast:
8	chr8:110643272..110646164-chr8:110646853..110649059,3	MCF-7	breast:
9	chr8:110552868..110555274-chr8:110604412..110606695,2	MCF-7	breast:
10	chr8:110588326..110591138-chr8:110601427..110604344,2	MCF-7	breast:
11	chr8:110639830..110641463-chr8:110642353..110644187,2	K562	blood:
12	chr8:110462528..110463405-chr8:110651980..110652480,2	MCF-7	breast:
13	chr8:110587443..110588480-chr8:110650468..110651460,3	MCF-7	breast:
14	chr8:110358952..110359590-chr8:110664334..110665002,4	MCF-7	breast:
15	chr8:110669997..110672035-chr8:110674199..110676102,2	MCF-7	breast:
16	chr8:110634308..110638739-chr8:110641463..110645115,4	MCF-7	breast:
17	chr8:110344899..110348479-chr8:110652629..110655762,4	MCF-7	breast:
18	chr8:110634308..110638739-chr8:110641463..110645115,4	MCF-7	breast:
19	chr8:110604317..110607760-chr8:110608079..110611073,4	MCF-7	breast:
20	chr8:110664832..110666386-chr8:110668699..110671644,3	K562	blood:
21	chr8:110586311..110588193-chr8:110645798..110647826,2	MCF-7	breast:
22	chr8:110631150..110633770-chr8:110636453..110640817,4	K562	blood:
23	chr8:110639830..110641463-chr8:110642353..110644187,2	K562	blood:
24	chr8:110604868..110607165-chr8:110611365..110613319,2	MCF-7	breast:
25	chr8:110597460..110599576-chr8:110604521..110607030,2	MCF-7	breast:
26	chr8:110626045..110628361-chr8:110643151..110644803,2	MCF-7	breast:
27	chr8:110632763..110635475-chr8:110652459..110654978,2	K562	blood:
28	chr8:110580193..110582706-chr8:110638450..110640225,2	MCF-7	breast:
29	chr8:110344019..110346826-chr8:110650680..110652185,2	K562	blood:
30	chr8:110609564..110612150-chr8:110618699..110620279,2	K562	blood:
31	chr8:110463988..110464714-chr8:110664335..110664899,2	MCF-7	breast:
32	chr8:110654758..110657420-chr8:110658925..110660931,2	K562	blood:
33	chr8:110603377..110605733-chr8:110607297..110608856,2	K562	blood:
34	chr8:110664332..110665340-chr8:110732244..110733184,5	MCF-7	breast:
35	chr8:110587269..110587781-chr8:110658115..110658651,2	MCF-7	breast:
36	chr8:110563214..110565678-chr8:110658219..110659984,2	K562	blood:
37	chr8:110643272..110646164-chr8:110646853..110649059,3	MCF-7	breast:
38	chr8:110358379..110359744-chr8:110664444..110665358,3	MCF-7	breast:
39	chr8:110343048..110346506-chr8:110655063..110657604,4	MCF-7	breast:
40	chr8:110344436..110346948-chr8:110603611..110606145,2	MCF-7	breast:
41	chr8:110649169..110652040-chr8:110653790..110655530,2	K562	blood:
42	chr8:110552227..110553856-chr8:110652244..110654868,2	MCF-7	breast:
43	chr8:110601011..110602738-chr8:110605572..110607359,2	K562	blood:
44	chr8:110601515..110604234-chr8:110611916..110615052,3	MCF-7	breast:
45	chr8:110623120..110625738-chr8:110638135..110640971,2	K562	blood:
46	chr8:110646850..110649452-chr8:110652359..110657793,4	K562	blood:
47	chr8:110356541..110358567-chr8:110652716..110654323,2	K562	blood:
48	chr8:110644089..110646105-chr8:110649563..110651332,2	K562	blood:
49	chr8:110345081..110347283-chr8:110656599..110658183,2	K562	blood:
50	chr8:110612107..110614990-chr8:110621772..110623731,2	MCF-7	breast:

No data

Variant related genes	Relation type
SYBU	TF binding region
ENSG00000252559	TF binding region
ENSG00000248050	TF binding region
SYBU	CpG island
ENSG00000252559	CpG island
ENSG00000248050	CpG island
ENSG00000147654	chromatin interactions
ENSG00000141027	chromatin interactions
ENSG00000120533	chromatin interactions
ENSG00000252559	chromatin interactions
ENSG00000165948	chromatin interactions
ENSG00000147642	chromatin interactions
ENSG00000120526	chromatin interactions
ENSG00000248050	chromatin interactions
ENSG00000109079	chromatin interactions
ENSG00000089737	chromatin interactions
ENSG00000124171	chromatin interactions

Extended variants
information (count: 3192 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:3192 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2844235	chr8:110594148-110594149	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs375425748	chr8:110594210-110594211	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs186473830	chr8:110594232-110594233	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs189672284	chr8:110594233-110594234	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs543908013	chr8:110594287-110594288	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs563600897	chr8:110594311-110594312	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs182376687	chr8:110594319-110594320	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs548116498	chr8:110594337-110594338	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs561522736	chr8:110594395-110594396	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs527626400	chr8:110594435-110594436	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs571866823	chr8:110594450-110594451	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs73700657	chr8:110594492-110594493	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs527841800	chr8:110594513-110594514	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs145681391	chr8:110594535-110594536	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs539018456	chr8:110594545-110594546	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs549871304	chr8:110594569-110594570	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs573580025	chr8:110594625-110594626	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs547684798	chr8:110594642-110594643	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs542481474	chr8:110594657-110594658	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs186220452	chr8:110594677-110594678	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs186603800	chr8:110594715-110594716	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs114297613	chr8:110594741-110594742	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs138361198	chr8:110594791-110594792	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs2844236	chr8:110594818-110594819	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs577986184	chr8:110594839-110594840	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs116236676	chr8:110594866-110594867	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs375793821	chr8:110594879-110594880	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs114266269	chr8:110594885-110594886	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs3779681	chr8:110594886-110594887	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs574076283	chr8:110594894-110594895	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs142760807	chr8:110594952-110594953	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs58483486	chr8:110595062-110595063	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs60859789	chr8:110595098-110595099	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs146045668	chr8:110595149-110595150	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs112452425	chr8:110595195-110595196	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs564012552	chr8:110595197-110595198	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs532959786	chr8:110595236-110595237	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs555868888	chr8:110595291-110595292	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs549547016	chr8:110595321-110595322	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs569612614	chr8:110595324-110595325	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs73700659	chr8:110595431-110595432	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs549093025	chr8:110595486-110595487	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs140028624	chr8:110595517-110595518	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs535182902	chr8:110595542-110595543	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs28585635	chr8:110595547-110595548	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs571879162	chr8:110595563-110595564	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs537725227	chr8:110595567-110595568	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs369391177	chr8:110595579-110595580	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs373334283	chr8:110595648-110595649	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs141769723	chr8:110595668-110595669	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Multiple myeloma	16461302	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Gastric cancer	22539939	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	21645411	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Prostate cancer	22341455	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1958 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:110553800-110613000	Weak transcription	NHLF	lung
2	chr8:110583800-110601600	Weak transcription	Duodenum Smooth Muscle	Duodenum
3	chr8:110586000-110598800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr8:110587800-110605800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr8:110588000-110594800	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr8:110588000-110600600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr8:110588200-110598200	Weak transcription	Ovary	ovary
8	chr8:110588200-110601600	Weak transcription	Left Ventricle	heart
9	chr8:110588600-110596600	Weak transcription	Colon Smooth Muscle	Colon
10	chr8:110589200-110598600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
11	chr8:110589800-110595200	Weak transcription	Psoas Muscle	Psoas
12	chr8:110589800-110598000	Weak transcription	Brain Substantia Nigra	brain
13	chr8:110589800-110598200	Weak transcription	Brain Cingulate Gyrus	brain
14	chr8:110589800-110601600	Weak transcription	Right Atrium	heart
15	chr8:110590000-110597800	Weak transcription	Pancreatic Islets	Pancreatic Islet
16	chr8:110590000-110605600	Weak transcription	K562	blood
17	chr8:110590200-110654800	Weak transcription	Lung	lung
18	chr8:110590800-110597800	Weak transcription	Brain Hippocampus Middle	brain
19	chr8:110591200-110601600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr8:110591600-110594600	Weak transcription	Adipose Nuclei	Adipose
21	chr8:110591600-110595200	Weak transcription	Fetal Muscle Leg	muscle
22	chr8:110591600-110596000	Weak transcription	HepG2	liver
23	chr8:110591600-110597000	Weak transcription	Rectal Smooth Muscle	rectum
24	chr8:110591600-110597600	Weak transcription	Colonic Mucosa	Colon
25	chr8:110591600-110598400	Weak transcription	Right Ventricle	heart
26	chr8:110591600-110599400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr8:110591600-110601600	Weak transcription	Skeletal Muscle Male	skeletal muscle
28	chr8:110591600-110609400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr8:110591800-110598200	Weak transcription	Fetal Stomach	stomach
30	chr8:110592000-110601400	Weak transcription	Brain Angular Gyrus	brain
31	chr8:110592200-110594600	Weak transcription	Brain Anterior Caudate	brain
32	chr8:110592200-110595800	Genic enhancers	Liver	Liver
33	chr8:110592200-110596800	Weak transcription	Fetal Intestine Large	intestine
34	chr8:110592200-110597400	Weak transcription	Brain Inferior Temporal Lobe	brain
35	chr8:110592200-110601600	Weak transcription	NHEK	skin
36	chr8:110592200-110604600	Weak transcription	Gastric	stomach
37	chr8:110592400-110594600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr8:110592400-110594600	Weak transcription	Stomach Smooth Muscle	stomach
39	chr8:110592400-110596600	Weak transcription	Fetal Brain Female	brain
40	chr8:110592400-110597600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr8:110592400-110601800	Weak transcription	Brain Germinal Matrix	brain
42	chr8:110592800-110597000	Weak transcription	Duodenum Mucosa	Duodenum
43	chr8:110593000-110595800	Weak transcription	Fetal Intestine Small	intestine
44	chr8:110593200-110594400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr8:110593200-110596200	Weak transcription	Small Intestine	intestine
46	chr8:110593200-110598600	Strong transcription	Cortex derived primary cultured neurospheres	brain
47	chr8:110593400-110594600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr8:110593400-110594800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr8:110593400-110595400	Weak transcription	Rectal Mucosa Donor 31	rectum
50	chr8:110593400-110597600	Weak transcription	Esophagus	oesophagus

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