Variant report

Variant	nsv1034185
Chromosome Location	chr8:47727123-47767022
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:262)
CpG islands
(count:306)
Chromatin interactive
region (count:0)
LncRNA
region (count:84)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:262 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr8:47750627-47750683	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr8:47742058-47742352	GM12878	blood:	n/a	n/a
3	BATF	chr8:47742543-47742780	GM12878	blood:	n/a	n/a
4	BATF	chr8:47741055-47741204	GM12878	blood:	n/a	n/a
5	BATF	chr8:47742166-47742315	GM12878	blood:	n/a	n/a
6	BATF	chr8:47738438-47738681	GM12878	blood:	n/a	chr8:47738534-47738545
7	BATF	chr8:47742552-47742702	GM12878	blood:	n/a	n/a
8	BCL11A	chr8:47742011-47742327	GM12878	blood:	n/a	n/a
9	BCL11A	chr8:47742493-47742715	GM12878	blood:	n/a	n/a
10	BCL11A	chr8:47742173-47742308	GM12878	blood:	n/a	n/a
11	BCL11A	chr8:47741045-47741214	GM12878	blood:	n/a	n/a
12	BCL11A	chr8:47741063-47741196	GM12878	blood:	n/a	n/a
13	BCL11A	chr8:47742558-47742696	GM12878	blood:	n/a	n/a
14	BHLHE40	chr8:47742538-47742866	HepG2	liver:	n/a	n/a
15	BHLHE40	chr8:47741998-47742438	HepG2	liver:	n/a	n/a
16	BHLHE40	chr8:47741043-47741216	HepG2	liver:	n/a	n/a
17	CEBPB	chr8:47766294-47766573	K562	blood:	n/a	chr8:47766390-47766401
18	CEBPB	chr8:47752678-47752878	K562	blood:	n/a	n/a
19	CEBPB	chr8:47733822-47733874	HepG2	liver:	n/a	n/a
20	CEBPB	chr8:47760272-47760591	A549	lung:	n/a	chr8:47760422-47760435 chr8:47760424-47760433 chr8:47760423-47760434 chr8:47760424-47760433 chr8:47760424-47760433 chr8:47760424-47760433 chr8:47760422-47760435 chr8:47760422-47760433 chr8:47760422-47760435 chr8:47760422-47760433
21	CEBPB	chr8:47729741-47729838	HepG2	liver:	n/a	n/a
22	CEBPB	chr8:47766240-47766570	A549	lung:	n/a	chr8:47766390-47766401
23	CEBPB	chr8:47767015-47767397	IMR90	lung:	n/a	chr8:47767152-47767163
24	CEBPB	chr8:47752236-47752796	HepG2	liver:	n/a	n/a
25	CEBPB	chr8:47753716-47755048	A549	lung:	n/a	n/a
26	CEBPB	chr8:47729582-47729782	IMR90	lung:	n/a	chr8:47729734-47729745
27	CEBPB	chr8:47732060-47732380	MCF-7	breast:	n/a	chr8:47732251-47732262
28	CEBPB	chr8:47766213-47766559	IMR90	lung:	n/a	chr8:47766390-47766401
29	CEBPB	chr8:47757356-47758245	A549	lung:	n/a	n/a
30	CEBPB	chr8:47728521-47729026	HepG2	liver:	n/a	n/a
31	CEBPB	chr8:47732177-47732382	H1-hESC	embryonic stem cell:	n/a	chr8:47732251-47732262
32	CEBPB	chr8:47754666-47755099	MCF-7	breast:	n/a	n/a
33	CEBPB	chr8:47731371-47731837	HepG2	liver:	n/a	n/a
34	CEBPB	chr8:47728857-47729192	A549	lung:	n/a	n/a
35	CEBPB	chr8:47760294-47760574	HepG2	liver:	n/a	chr8:47760422-47760435 chr8:47760424-47760433 chr8:47760423-47760434 chr8:47760424-47760433 chr8:47760424-47760433 chr8:47760424-47760433 chr8:47760422-47760435 chr8:47760422-47760433 chr8:47760422-47760435 chr8:47760422-47760433
36	CEBPB	chr8:47760243-47760576	K562	blood:	n/a	chr8:47760422-47760435 chr8:47760424-47760433 chr8:47760423-47760434 chr8:47760424-47760433 chr8:47760424-47760433 chr8:47760424-47760433 chr8:47760422-47760435 chr8:47760422-47760433 chr8:47760422-47760435 chr8:47760422-47760433
37	CEBPB	chr8:47757331-47758282	HepG2	liver:	n/a	n/a
38	CEBPB	chr8:47732072-47732430	HepG2	liver:	n/a	chr8:47732251-47732262
39	CEBPB	chr8:47737694-47737724	HepG2	liver:	n/a	n/a
40	CEBPB	chr8:47730645-47730867	HepG2	liver:	n/a	n/a
41	CEBPB	chr8:47752209-47752790	A549	lung:	n/a	n/a
42	CEBPB	chr8:47750868-47751216	HepG2	liver:	n/a	chr8:47751033-47751044
43	CEBPB	chr8:47755769-47755984	A549	lung:	n/a	n/a
44	CEBPB	chr8:47732078-47732422	A549	lung:	n/a	chr8:47732251-47732262
45	CEBPB	chr8:47730627-47730869	A549	lung:	n/a	n/a
46	CEBPB	chr8:47732135-47732429	IMR90	lung:	n/a	chr8:47732251-47732262
47	CEBPB	chr8:47754701-47755059	IMR90	lung:	n/a	n/a
48	CEBPB	chr8:47766223-47766564	HepG2	liver:	n/a	chr8:47766390-47766401
49	CEBPB	chr8:47753754-47755047	HepG2	liver:	n/a	n/a
50	CEBPB	chr8:47750894-47751193	IMR90	lung:	n/a	chr8:47751033-47751044

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:47748435-47748485	GM06990	blood:	n/a
2	chr8:47748435-47748485	GM06990	blood:	n/a
3	chr8:47748435-47748485	GM12878	blood:	n/a
4	chr8:47751494-47751544	HEEpiC	esophagus:	n/a
5	chr8:47751494-47751544	NHBE	bronchial:	n/a
6	chr8:47761906-47761956	HUVEC	blood vessel:	n/a
7	chr8:47751953-47752003	SK-N-SH	brain:	n/a
8	chr8:47761906-47761956	RPTEC	kidney:	n/a
9	chr8:47748435-47748485	Jurkat	blood:	n/a
10	chr8:47751494-47751544	SAEC	small airway:	n/a
11	chr8:47751953-47752003	IMR90	lung:	fetal
12	chr8:47751623-47751673	U87	brain:	n/a
13	chr8:47761906-47761956	Jurkat	blood:	n/a
14	chr8:47751494-47751544	HUVEC	blood vessel:	n/a
15	chr8:47761906-47761956	AoSMC	blood vessel:	n/a
16	chr8:47751623-47751673	T-47D	breast:	n/a
17	chr8:47751953-47752003	Caco-2	colon:	n/a
18	chr8:47761906-47761956	GM12878	blood:	n/a
19	chr8:47751623-47751673	HRCEpiC	kidney:	n/a
20	chr8:47751953-47752003	HEEpiC	esophagus:	n/a
21	chr8:47748435-47748485	H1-hESC	embryonic stem cell:	embryo
22	chr8:47751953-47752003	H1-hESC	embryonic stem cell:	embryo
23	chr8:47751494-47751544	HepG2	liver:	n/a
24	chr8:47761906-47761956	NT2-D1	testis:	n/a
25	chr8:47761906-47761956	Hepatocyte	liver:	n/a
26	chr8:47761906-47761956	HCF	heart:	n/a
27	chr8:47751953-47752003	ECC-1	luminal epithelium:	n/a
28	chr8:47751623-47751673	Hepatocyte	liver:	n/a
29	chr8:47751494-47751544	LNCaP	prostate:	n/a
30	chr8:47751953-47752003	NB4	blood:	n/a
31	chr8:47751494-47751544	GM19239	blood:	n/a
32	chr8:47748435-47748485	Caco-2	colon:	n/a
33	chr8:47751623-47751673	IMR90	lung:	fetal
34	chr8:47751623-47751673	HMEC	breast:	n/a
35	chr8:47751953-47752003	GM12878	blood:	n/a
36	chr8:47751953-47752003	HCT-116	colon:	n/a
37	chr8:47751953-47752003	AG09319	gingival:	n/a
38	chr8:47748435-47748485	HCF	heart:	n/a
39	chr8:47751953-47752003	HMEC	breast:	n/a
40	chr8:47751953-47752003	HRPEpiC	eye:	n/a
41	chr8:47751623-47751673	ovcar-3	ovarian:	n/a
42	chr8:47751953-47752003	GM19239	blood:	n/a
43	chr8:47761906-47761956	GM19239	blood:	n/a
44	chr8:47761906-47761956	PrEC	prostate:	n/a
45	chr8:47761906-47761956	BE2_C	brain:	n/a
46	chr8:47761906-47761956	HRPEpiC	eye:	n/a
47	chr8:47751494-47751544	HCT-116	colon:	n/a
48	chr8:47751953-47752003	MCF-7	breast:	n/a
49	chr8:47751953-47752003	AG09309	skin:	n/a
50	chr8:47751494-47751544	PrEC	prostate:	n/a

No data

(count:84 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-1134I14.8.1-3	chr8:47753899-47753974	NONHSAT126421
2	lnc-RP11-1134I14.8.1-3	chr8:47754972-47755048	ENSG00000253314.1
3	lnc-RP11-1134I14.8.1-3	chr8:47752667-47752748	ENSG00000253314.1
4	lnc-RP11-1134I14.8.1-3	chr8:47754972-47755048	ENSG00000253314.1
5	lnc-RP11-1134I14.8.1-3	chr8:47762290-47762365	ENSG00000253314.1
6	lnc-RP11-1134I14.8.1-3	chr8:47757651-47757703	NONHSAT126419
7	lnc-RP11-1134I14.8.1-3	chr8:47759598-47759722	NONHSAT126415
8	lnc-RP11-1134I14.8.1-3	chr8:47766386-47766763	NONHSAT126424
9	lnc-RP11-350F16.2.1-5	chr8:47738850-47740031	NONHSAT126413
10	lnc-RP11-1134I14.8.1-3	chr8:47765729-47765991	NONHSAT126421
11	lnc-RP11-1134I14.8.1-3	chr8:47759598-47759722	NONHSAT126419
12	lnc-RP11-1134I14.8.1-3	chr8:47759598-47759722	ENSG00000253314.1
13	lnc-RP11-1134I14.8.1-3	chr8:47757651-47757703	NR_027013
14	lnc-RP11-1134I14.8.1-3	chr8:47757651-47757703	NONHSAT126420
15	lnc-RP11-1134I14.8.1-3	chr8:47759598-47759688	ENSG00000253314.1
16	lnc-RP11-1134I14.8.1-3	chr8:47760406-47761152	ENSG00000253314.1
17	lnc-RP11-1134I14.8.1-3	chr8:47765729-47765929	NR_027013
18	lnc-RP11-1134I14.8.1-8	chr8:47750410-47750827	NONHSAT126417
19	lnc-RP11-1134I14.8.1-3	chr8:47754972-47755048	ENSG00000253314.1
20	lnc-RP11-1134I14.8.1-3	chr8:47759598-47759722	ENSG00000253314.1
21	lnc-RP11-1134I14.8.1-3	chr8:47762290-47762365	NONHSAT126421
22	lnc-RP11-1134I14.8.1-3	chr8:47759598-47759722	NONHSAT126420
23	lnc-RP11-1134I14.8.1-3	chr8:47760406-47761152	NONHSAT126420
24	lnc-RP11-1134I14.8.1-3	chr8:47766092-47766216	NONHSAT126421
25	lnc-RP11-1134I14.8.1-3	chr8:47752667-47752748	NONHSAT126415
26	lnc-RP11-1134I14.8.1-3	chr8:47765729-47765991	NONHSAT126424
27	lnc-RP11-1134I14.8.1-3	chr8:47759598-47759722	NONHSAT126421
28	lnc-RP11-1134I14.8.1-3	chr8:47762290-47762365	NONHSAT126423
29	lnc-RP11-1134I14.8.1-3	chr8:47753899-47753974	NR_027013
30	lnc-RP11-1134I14.8.1-3	chr8:47752667-47752748	NONHSAT126420
31	lnc-RP11-1134I14.8.1-3	chr8:47765729-47765929	ENSG00000253314.1
32	lnc-RP11-1134I14.8.1-3	chr8:47752497-47752557	ENSG00000253314.1
33	lnc-RP11-1134I14.8.1-3	chr8:47754972-47755048	NONHSAT126415
34	lnc-RP11-1134I14.8.1-3	chr8:47760406-47760523	ENSG00000253314.1
35	lnc-RP11-1134I14.8.1-3	chr8:47752667-47752748	ENSG00000253314.1
36	lnc-RP11-1134I14.8.1-3	chr8:47748371-47748420	NONHSAT126415
37	lnc-RP11-1134I14.8.1-3	chr8:47762290-47762365	NR_027013
38	lnc-RP11-1134I14.8.1-3	chr8:47752667-47752748	ENSG00000253314.1
39	lnc-RP11-1134I14.8.1-3	chr8:47753899-47753974	NONHSAT126420
40	lnc-RP11-1134I14.8.1-3	chr8:47754972-47755048	ENSG00000253314.1
41	lnc-RP11-1134I14.8.1-3	chr8:47754972-47755048	NR_027013
42	lnc-RP11-1134I14.8.1-3	chr8:47752667-47752748	ENSG00000253314.1
43	lnc-RP11-1134I14.8.1-3	chr8:47752667-47752748	NONHSAT126419
44	lnc-RP11-1134I14.8.1-3	chr8:47759598-47759722	NR_027013
45	lnc-RP11-1134I14.8.1-3	chr8:47766092-47766220	NONHSAT126423
46	lnc-RP11-1134I14.8.1-3	chr8:47754972-47755048	NONHSAT126419
47	lnc-RP11-1134I14.8.1-3	chr8:47752486-47752557	NONHSAT126419
48	lnc-RP11-1134I14.8.1-3	chr8:47760896-47761152	NONHSAT126423
49	lnc-RP11-1134I14.8.1-3	chr8:47766386-47767407	NONHSAT126421
50	lnc-RP11-1134I14.8.1-3	chr8:47762290-47762365	ENSG00000253314.1

No data

Variant related genes	Relation type
MTND1P7	TF binding region
MTND6P20	TF binding region
LINC00293	TF binding region
RNU6-656P	TF binding region
ENSG00000254118	TF binding region
MTND1P7	CpG island
MTND6P20	CpG island
LINC00293	CpG island
RNU6-656P	CpG island
ENSG00000254118	CpG island
USO1	miRNA target sites

Extended variants
information (count: 1046 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:1046 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs145094969	chr8:47728909-47728910	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs551192973	chr8:47728913-47728914	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs566786967	chr8:47728948-47728949	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs191009018	chr8:47728957-47728958	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs551452903	chr8:47728978-47728979	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs150959937	chr8:47728985-47728986	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs375655009	chr8:47728991-47728992	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs181763922	chr8:47729010-47729011	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs140804952	chr8:47729085-47729086	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs557213664	chr8:47729089-47729090	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs186460519	chr8:47729136-47729137	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs191435519	chr8:47729141-47729142	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs183756550	chr8:47729200-47729201	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs73676245	chr8:47729213-47729214	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs573130181	chr8:47729217-47729218	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs113547297	chr8:47729219-47729220	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs537026267	chr8:47729256-47729257	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs577202851	chr8:47729267-47729268	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs11990120	chr8:47729355-47729356	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs562969216	chr8:47729365-47729366	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs550898568	chr8:47729368-47729369	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs541977560	chr8:47729385-47729386	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs560315851	chr8:47729389-47729390	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs527971019	chr8:47729395-47729396	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs567918025	chr8:47729397-47729398	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs564707967	chr8:47729435-47729436	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs532104821	chr8:47729468-47729469	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs369181047	chr8:47729483-47729484	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs550322255	chr8:47729504-47729505	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs568895172	chr8:47729515-47729516	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs536358134	chr8:47729600-47729601	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs535594107	chr8:47729626-47729627	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs536468925	chr8:47729631-47729632	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs553486698	chr8:47729632-47729633	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs111829014	chr8:47729650-47729651	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs187889526	chr8:47729662-47729663	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs11777235	chr8:47729693-47729694	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs35969444	chr8:47729695-47729696	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs191558799	chr8:47729697-47729698	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs558841586	chr8:47729706-47729707	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs376330050	chr8:47729716-47729717	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs182171746	chr8:47729746-47729747	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs201952445	chr8:47729817-47729818	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs556290727	chr8:47729827-47729828	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs534748590	chr8:47729895-47729896	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs140382452	chr8:47729902-47729903	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs541961621	chr8:47729910-47729911	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs56844665	chr8:47729931-47729932	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs71239878	chr8:47729974-47729975	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs552301524	chr8:47730669-47730670	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
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
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Oral cancer	21386901	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Lung cancer	18438408	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Salivary gland tumor	18059337	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
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
abnormal development	18461090	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Medulloblastoma	20607354	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
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	20409316	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
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Tetralogy of Fallot	22912587	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:47733800-47736400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
2	chr8:47751400-47752000	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
3	chr8:47751400-47753800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr8:47753200-47753800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
5	chr8:47754000-47755000	Enhancers	Placenta	Placenta
6	chr8:47755000-47757000	Weak transcription	Placenta	Placenta
7	chr8:47757000-47758200	Enhancers	Placenta	Placenta
8	chr8:47758200-47759400	Weak transcription	Placenta	Placenta
9	chr8:47759200-47761400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
10	chr8:47760000-47760400	Active TSS	Fetal Heart	heart
11	chr8:47761400-47762000	Weak transcription	Placenta	Placenta
12	chr8:47762000-47763400	Enhancers	Placenta	Placenta
13	chr8:47763400-47767400	Weak transcription	Placenta	Placenta
14	chr8:47764200-47764400	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
15	chr8:47765200-47765400	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell

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