Variant report

Variant	nsv831258
Chromosome Location	chr8:20754932-20940380
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:904)
CpG islands
(count:61)
Chromatin interactive
region (count:25)
LncRNA
region (count:87)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:904 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:20898739-20898891	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:20898739-20898837	K562	blood:	n/a	n/a
3	ATF1	chr8:20809628-20809937	K562	blood:	n/a	n/a
4	ATF3	chr8:20891514-20891728	K562	blood:	n/a	n/a
5	BACH1	chr8:20813151-20813198	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL3	chr8:20871346-20871797	GM12878	blood:	n/a	n/a
7	BCL3	chr8:20836598-20836879	GM12878	blood:	n/a	n/a
8	BCL3	chr8:20871364-20871889	GM12878	blood:	n/a	n/a
9	BHLHE40	chr8:20898691-20898929	GM12878	blood:	n/a	chr8:20898790-20898806
10	BHLHE40	chr8:20891661-20891672	K562	blood:	n/a	n/a
11	BHLHE40	chr8:20898617-20899322	K562	blood:	n/a	chr8:20898790-20898806
12	BRCA1	chr8:20898669-20898930	H1-hESC	embryonic stem cell:	n/a	n/a
13	BRCA1	chr8:20871437-20871485	GM12878	blood:	n/a	n/a
14	CCNT2	chr8:20875218-20875595	K562	blood:	n/a	n/a
15	CCNT2	chr8:20809452-20809864	K562	blood:	n/a	chr8:20809683-20809703
16	CEBPB	chr8:20830066-20830350	HepG2	liver:	n/a	chr8:20830220-20830231
17	CEBPB	chr8:20810953-20811181	K562	blood:	n/a	chr8:20811090-20811101
18	CEBPB	chr8:20810677-20811262	IMR90	lung:	n/a	chr8:20811090-20811101
19	CEBPB	chr8:20898717-20898900	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr8:20757415-20757431	A549	lung:	n/a	n/a
21	CEBPB	chr8:20913882-20914203	HepG2	liver:	n/a	n/a
22	CEBPB	chr8:20830191-20830296	H1-hESC	embryonic stem cell:	n/a	chr8:20830220-20830231
23	CEBPB	chr8:20810638-20811217	HepG2	liver:	n/a	chr8:20811090-20811101
24	CEBPB	chr8:20768532-20768761	IMR90	lung:	n/a	chr8:20768654-20768665
25	CEBPB	chr8:20852924-20853124	HepG2	liver:	n/a	n/a
26	CEBPB	chr8:20768508-20768763	K562	blood:	n/a	chr8:20768654-20768665
27	CEBPB	chr8:20852513-20852598	HepG2	liver:	n/a	n/a
28	CEBPB	chr8:20913900-20914163	K562	blood:	n/a	n/a
29	CEBPB	chr8:20913887-20914170	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr8:20916891-20917209	HepG2	liver:	n/a	chr8:20917030-20917041
31	CEBPB	chr8:20809083-20809266	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr8:20768496-20768814	HepG2	liver:	n/a	chr8:20768654-20768665
33	CEBPB	chr8:20916875-20917150	IMR90	lung:	n/a	chr8:20917030-20917041
34	CEBPB	chr8:20810943-20811214	A549	lung:	n/a	chr8:20811090-20811101
35	CEBPB	chr8:20852958-20853147	K562	blood:	n/a	n/a
36	CEBPB	chr8:20916934-20917174	H1-hESC	embryonic stem cell:	n/a	chr8:20917030-20917041
37	CEBPB	chr8:20795561-20795603	HepG2	liver:	n/a	n/a
38	CEBPB	chr8:20881612-20881775	K562	blood:	n/a	n/a
39	CEBPB	chr8:20905661-20905759	IMR90	lung:	n/a	n/a
40	CEBPB	chr8:20768506-20768831	A549	lung:	n/a	chr8:20768654-20768665
41	CEBPB	chr8:20913877-20914202	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr8:20913845-20914246	MCF-7	breast:	n/a	n/a
43	CEBPB	chr8:20913886-20914184	A549	lung:	n/a	n/a
44	CEBPB	chr8:20846099-20846340	HepG2	liver:	n/a	n/a
45	CEBPB	chr8:20916902-20917149	K562	blood:	n/a	chr8:20917030-20917041
46	CEBPB	chr8:20852997-20853024	A549	lung:	n/a	n/a
47	CEBPB	chr8:20929353-20929765	HepG2	liver:	n/a	chr8:20929621-20929634 chr8:20929621-20929632
48	CEBPB	chr8:20925030-20925226	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr8:20840086-20840263	HepG2	liver:	n/a	chr8:20840222-20840233
50	CEBPD	chr8:20809552-20809922	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:20899208-20899258	HL-60	blood:	n/a
2	chr8:20899208-20899258	A549	lung:	n/a
3	chr8:20899208-20899258	AG04450	lung:	fetal
4	chr8:20899208-20899258	IMR90	lung:	fetal
5	chr8:20899208-20899258	SK-N-MC	brain:	n/a
6	chr8:20899208-20899258	SK-N-SH_RA	brain:	n/a
7	chr8:20899208-20899258	HIPEpiC	eye:	n/a
8	chr8:20899208-20899258	HUVEC	blood vessel:	n/a
9	chr8:20899208-20899258	GM19239	blood:	n/a
10	chr8:20899208-20899258	T-47D	breast:	n/a
11	chr8:20899208-20899258	AG04449	skin:	fetal
12	chr8:20899208-20899258	HRPEpiC	eye:	n/a
13	chr8:20899208-20899258	RPTEC	kidney:	n/a
14	chr8:20899208-20899258	MCF10A-Er-Src	breast:	n/a
15	chr8:20899208-20899258	Hepatocyte	liver:	n/a
16	chr8:20899208-20899258	HCF	heart:	n/a
17	chr8:20899208-20899258	Jurkat	blood:	n/a
18	chr8:20899208-20899258	LNCaP	prostate:	n/a
19	chr8:20899208-20899258	HEK293	kidney:	embryo
20	chr8:20899208-20899258	H1-hESC	embryonic stem cell:	embryo
21	chr8:20899208-20899258	GM12891	blood:	n/a
22	chr8:20899208-20899258	ECC-1	luminal epithelium:	n/a
23	chr8:20899208-20899258	HRE	kidney:	n/a
24	chr8:20899208-20899258	CMK	blood:	n/a
25	chr8:20899208-20899258	HepG2	liver:	n/a
26	chr8:20899208-20899258	HPAEpiC	pulmonary alveolar:	n/a
27	chr8:20899208-20899258	HNPCEpiC	eye:	n/a
28	chr8:20899208-20899258	SK-N-SH	brain:	n/a
29	chr8:20899208-20899258	NHBE	bronchial:	n/a
30	chr8:20899208-20899258	PANC-1	pancreas:	n/a
31	chr8:20899208-20899258	MCF-7	breast:	n/a
32	chr8:20899208-20899258	PFSK-1	brain:	n/a
33	chr8:20899208-20899258	AG09319	gingival:	n/a
34	chr8:20899208-20899258	Caco-2	colon:	n/a
35	chr8:20899208-20899258	U87	brain:	n/a
36	chr8:20899208-20899258	SKMC	muscle:	n/a
37	chr8:20899208-20899258	BE2_C	brain:	n/a
38	chr8:20899208-20899258	HEEpiC	esophagus:	n/a
39	chr8:20899208-20899258	AG09309	skin:	n/a
40	chr8:20899208-20899258	NHDF-neo	bronchial:	n/a
41	chr8:20899208-20899258	GM12892	blood:	n/a
42	chr8:20899208-20899258	NH-A	brain:	n/a
43	chr8:20899208-20899258	PrEC	prostate:	n/a
44	chr8:20899208-20899258	Hela-S3	cervix:	n/a
45	chr8:20899208-20899258	HRCEpiC	kidney:	n/a
46	chr8:20899208-20899258	AoSMC	blood vessel:	n/a
47	chr8:20899208-20899258	GM12878	blood:	n/a
48	chr8:20899208-20899258	NT2-D1	testis:	n/a
49	chr8:20899208-20899258	BJ	skin:	n/a
50	chr8:20899208-20899258	GM06990	blood:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:20297170..20297886-chr8:20854968..20855533,2	MCF-7	breast:
2	chr8:20897307..20899039-chr8:20900346..20903316,2	K562	blood:
3	chr8:20856229..20857904-chr8:20875184..20876772,2	K562	blood:
4	chr8:20750920..20753775-chr8:20759115..20761137,3	K562	blood:
5	chr8:20856229..20857904-chr8:20875184..20876772,2	K562	blood:
6	chr8:20897307..20899039-chr8:20900346..20903316,2	K562	blood:
7	chr8:20781724..20783659-chr8:20784151..20785678,2	K562	blood:
8	chr8:20919649..20922445-chr8:20924691..20927492,3	K562	blood:
9	chr8:20806761..20808497-chr8:20810222..20812992,2	K562	blood:
10	chr8:20767548..20769104-chr8:20769526..20772463,2	MCF-7	breast:
11	chr8:20898532..20899166-chr8:21104084..21105006,2	MCF-7	breast:
12	chr8:20893311..20895358-chr8:20895433..20897444,2	K562	blood:
13	chr8:20898154..20898861-chr8:21641597..21642547,2	MCF-7	breast:
14	chr8:20920073..20922021-chr8:20924691..20926689,2	K562	blood:
15	chr8:20400181..20400690-chr8:20854628..20855500,2	MCF-7	breast:
16	chr8:20781724..20783659-chr8:20784151..20785678,2	K562	blood:
17	chr20:55800391..55800924-chr8:20778716..20779696,2	MCF-7	breast:
18	chr8:20831135..20833950-chr8:20835824..20837842,2	K562	blood:
19	chr8:20737626..20740045-chr8:20787296..20789914,2	K562	blood:
20	chr8:20920073..20922021-chr8:20924691..20926689,2	K562	blood:
21	chr8:20767548..20769104-chr8:20769526..20772463,2	MCF-7	breast:
22	chr8:20839365..20841858-chr8:20843930..20846390,2	K562	blood:
23	chr8:20839365..20841858-chr8:20843930..20846390,2	K562	blood:
24	chr8:20893311..20895358-chr8:20895433..20897444,2	K562	blood:
25	chr8:20919649..20922445-chr8:20924691..20927492,3	K562	blood:

(count:87 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATP6V1B2-5	chr8:20811352-20811586	XLOC_006734
2	lnc-ATP6V1B2-4	chr8:20798939-20799011	ENSG00000254260
3	lnc-ATP6V1B2-5	chr8:20813196-20813345	ENSG00000253147
4	lnc-ATP6V1B2-5	chr8:20825695-20826830	NONHSAT125407
5	lnc-ATP6V1B2-5	chr8:20820144-20820412	NONHSAT125418
6	lnc-LZTS1-2	chr8:20810156-20810427	ENSG00000254092
7	lnc-ATP6V1B2-5	chr8:20852291-20852449	XLOC_006734
8	lnc-LZTS1-2	chr8:20831244-20831388	ENSG00000254092
9	lnc-ATP6V1B2-9	chr8:20855632-20855866	l_3558_chr8:20855416-20870707_testes
10	lnc-ATP6V1B2-5	chr8:20811137-20811204	XLOC_006734
11	lnc-ATP6V1B2-9	chr8:20857476-20857627	l_3558_chr8:20855416-20870707_testes
12	lnc-ATP6V1B2-9	chr8:20864572-20864692	l_3558_chr8:20855416-20870707_testes
13	lnc-ATP6V1B2-4	chr8:20806210-20806304	ENSG00000254260
14	lnc-ATP6V1B2-5	chr8:20843922-20843997	XLOC_006734
15	lnc-ATP6V1B2-5	chr8:20826298-20826427	XLOC_006734
16	lnc-ATP6V1B2-5	chr8:20811153-20811204	ENSG00000253147
17	lnc-ATP6V1B2-5	chr8:20813196-20813346	XLOC_006734
18	lnc-ATP6V1B2-5	chr8:20832315-20832531	NONHSAT125421
19	lnc-ATP6V1B2-5	chr8:20810638-20811204	NONHSAT125407
20	lnc-ATP6V1B2-5	chr8:20826298-20826482	NONHSAT125418
21	lnc-ATP6V1B2-5	chr8:20831860-20832033	XLOC_006734
22	lnc-ATP6V1B2-5	chr8:20811352-20811590	ENSG00000253147
23	lnc-ATP6V1B2-5	chr8:20811154-20811204	XLOC_006734
24	lnc-ATP6V1B2-5	chr8:20811523-20811586	ENSG00000254026
25	lnc-GFRA2-2	chr8:20917383-20917446	XLOC_007019
26	lnc-ATP6V1B2-10	chr8:20896820-20896910	refGeneNc_4250_NR_033894
27	lnc-ATP6V1B2-6	chr8:20884720-20884808	ENSG00000254040
28	lnc-ATP6V1B2-10	chr8:20885248-20885897	refGeneNc_4250_NR_033894
29	lnc-LZTS1-4	chr8:20791946-20792348	NONHSAT125404
30	lnc-ATP6V1B2-5	chr8:20812727-20812776	XLOC_006734
31	lnc-ATP6V1B2-5	chr8:20813385-20813631	ENSG00000254026
32	lnc-ATP6V1B2-6	chr8:20886043-20886100	ENSG00000254040
33	lnc-GFRA2-6	chr8:20875524-20876313	l_3557_chr8:20853997-20856467_brain
34	lnc-ATP6V1B2-5	chr8:20831497-20832164	XLOC_006734
35	lnc-ATP6V1B2-5	chr8:20813196-20813345	ENSG00000253147
36	lnc-ATP6V1B2-10	chr8:20888202-20888277	refGeneNc_4250_NR_033894
37	lnc-ATP6V1B2-5	chr8:20810937-20811204	XLOC_006734
38	lnc-ATP6V1B2-5	chr8:20820292-20820412	ENSG00000254026
39	lnc-ATP6V1B2-5	chr8:20820292-20820406	ENSG00000253147
40	lnc-ATP6V1B2-6	chr8:20886417-20886569	ENSG00000254040
41	lnc-ATP6V1B2-5	chr8:20840968-20841617	XLOC_006734
42	lnc-ATP6V1B2-5	chr8:20852540-20852630	XLOC_006734
43	lnc-ATP6V1B2-5	chr8:20813195-20813631	NONHSAT125407
44	lnc-LZTS1-2	chr8:20810905-20811014	XLOC_007018
45	lnc-ATP6V1B2-5	chr8:20820292-20820412	XLOC_006734
46	lnc-ATP6V1B2-5	chr8:20826298-20826415	ENSG00000253147
47	lnc-ATP6V1B2-10	chr8:20875777-20876444	refGeneNc_4250_NR_033894
48	lnc-ATP6V1B2-5	chr8:20852291-20852334	XLOC_006734
49	lnc-ATP6V1B2-6	chr8:20880807-20881087	ENSG00000254040
50	lnc-ATP6V1B2-4	chr8:20800453-20800763	ENSG00000254260

No data

Variant related genes	Relation type
ENSG00000254260	TF binding region
TMEM97P2	TF binding region
ENSG00000254026	TF binding region
ENSG00000253147	TF binding region
ENSG00000253199	TF binding region
ENSG00000254092	TF binding region
ENSG00000254040	TF binding region
ENSG00000254260	CpG island
TMEM97P2	CpG island
ENSG00000254026	CpG island
ENSG00000253147	CpG island
ENSG00000253199	CpG island
ENSG00000254092	CpG island
ENSG00000254040	CpG island
ENSG00000253199	chromatin interactions
ENSG00000254026	chromatin interactions
ENSG00000254092	chromatin interactions
ENSG00000253147	chromatin interactions
HIF1AN	miRNA target sites
RAB14	miRNA target sites
CAB39	miRNA target sites
SCD	miRNA target sites
GRB2	miRNA target sites
BMPR2	miRNA target sites
LDLR	miRNA target sites
SCARB1	miRNA target sites
TP53	miRNA target sites

Extended variants
information (count: 5744 )
Associated
traits (count: 118 )

Variant overlapped rSNPs/rCNVs (count:5744 , 50 per page) page: 1 2 3 4 5 6 7 ... 115

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs550022799	chr8:20760610-20760611	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs561947515	chr8:20760650-20760651	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs529490809	chr8:20760652-20760653	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs150602737	chr8:20760670-20760671	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs188412770	chr8:20760675-20760676	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs528459728	chr8:20760689-20760690	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs190468394	chr8:20760729-20760730	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs138732671	chr8:20760758-20760759	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs570316253	chr8:20760772-20760773	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs538145350	chr8:20760786-20760787	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs556546766	chr8:20760797-20760798	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs571865983	chr8:20760823-20760824	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs149527177	chr8:20760833-20760834	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs34489681	chr8:20760870-20760871	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs77876645	chr8:20760897-20760898	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs555858735	chr8:20760919-20760920	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs572524444	chr8:20760925-20760926	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs551186687	chr8:20760930-20760931	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs75098118	chr8:20760989-20760990	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs564515949	chr8:20760997-20760998	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs147214402	chr8:20761060-20761061	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs577281196	chr8:20761074-20761075	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs569328437	chr8:20761075-20761076	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs140636251	chr8:20761097-20761098	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs562082177	chr8:20761148-20761149	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs546383681	chr8:20761189-20761190	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs183059229	chr8:20761203-20761204	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs537187781	chr8:20761250-20761251	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs547609908	chr8:20761255-20761256	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs73627801	chr8:20761287-20761288	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs527396356	chr8:20761298-20761299	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs545095082	chr8:20761339-20761340	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs551944311	chr8:20761363-20761364	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs570525381	chr8:20761368-20761369	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs187367781	chr8:20761394-20761395	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs73668274	chr8:20761448-20761449	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs549787946	chr8:20761513-20761514	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs4961417	chr8:20761608-20761609	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs114816607	chr8:20761632-20761633	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs144404064	chr8:20761638-20761639	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs565698513	chr8:20761641-20761642	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs73668275	chr8:20761661-20761662	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs147414770	chr8:20761668-20761669	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs576116735	chr8:20761696-20761697	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs543444130	chr8:20761711-20761712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs192330740	chr8:20761733-20761734	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs574016051	chr8:20761738-20761739	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs553324683	chr8:20761766-20761767	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs559906046	chr8:20761767-20761768	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs116646743	chr8:20761824-20761825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:118)

Disease	PMID	Source
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Epilepsy	22083797	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	17603634	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	17550852	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21364760	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cancer	18840272	CNVD
Breast cancer	19602461	CNVD
Osteosarcoma	19286668	CNVD
Prostate cancer	19242612	CNVD
Prostate cancer	19258508	CNVD
small cell lung cancer	20016488	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Gastric adenocarcinoma	19115996	CNVD
Colorectal cancer	19455253	CNVD
Melanoma	20688739	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:511 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:20760600-20761800	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr8:20760800-20761200	Enhancers	Brain Inferior Temporal Lobe	brain
3	chr8:20761400-20764200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr8:20762400-20762600	Enhancers	H9 Cell Line	embryonic stem cell
5	chr8:20763400-20763600	Enhancers	H9 Cell Line	embryonic stem cell
6	chr8:20763400-20763800	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr8:20764200-20765000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr8:20765000-20765200	Enhancers	H9 Cell Line	embryonic stem cell
9	chr8:20765200-20765400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr8:20765400-20774000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr8:20765600-20766000	Enhancers	Rectal Mucosa Donor 29	rectum
12	chr8:20766000-20766600	Enhancers	Rectal Mucosa Donor 31	rectum
13	chr8:20767600-20767800	Enhancers	Left Ventricle	heart
14	chr8:20767800-20768200	Enhancers	Fetal Heart	heart
15	chr8:20768000-20768400	Enhancers	Brain Germinal Matrix	brain
16	chr8:20768200-20769800	Weak transcription	Fetal Heart	heart
17	chr8:20769800-20771800	Enhancers	Fetal Heart	heart
18	chr8:20770000-20771400	Enhancers	Left Ventricle	heart
19	chr8:20772800-20773600	Enhancers	Primary hematopoietic stem cells short term culture	blood
20	chr8:20772800-20773600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr8:20773000-20773600	Enhancers	Monocytes-CD14+_RO01746	blood
22	chr8:20773000-20773800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr8:20773000-20774600	Enhancers	Primary monocytes fromperipheralblood	blood
24	chr8:20773000-20774800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr8:20773400-20774200	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr8:20774000-20774800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr8:20774000-20774800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr8:20774000-20775000	Enhancers	H1 Cell Line	embryonic stem cell
29	chr8:20774200-20774800	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr8:20774200-20774800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr8:20774200-20775000	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr8:20774200-20775200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr8:20774400-20774800	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr8:20774800-20777200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr8:20775200-20775600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr8:20775600-20775800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr8:20775800-20776400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr8:20776400-20777600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr8:20781600-20781800	Enhancers	Primary hematopoietic stem cells	blood
40	chr8:20781600-20782400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr8:20781800-20782400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr8:20782400-20785400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr8:20782400-20785400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr8:20785400-20786600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr8:20785400-20786800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr8:20785600-20786400	Enhancers	Primary hematopoietic stem cells	blood
47	chr8:20785800-20786200	Enhancers	Primary hematopoietic stem cells short term culture	blood
48	chr8:20796000-20797800	Enhancers	Rectal Mucosa Donor 31	rectum
49	chr8:20796200-20798000	Enhancers	Rectal Mucosa Donor 29	rectum
50	chr8:20796800-20797400	Enhancers	Colonic Mucosa	Colon

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