Variant report

Variant	nsv1028897
Chromosome Location	chr8:47722290-47801967
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:386)
CpG islands
(count:305)
Chromatin interactive
region (count:0)
LncRNA
region (count:85)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:386 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr8:47770297-47770313	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr8:47750627-47750683	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr8:47742058-47742352	GM12878	blood:	n/a	n/a
4	BATF	chr8:47738438-47738681	GM12878	blood:	n/a	chr8:47738534-47738545
5	BATF	chr8:47742543-47742780	GM12878	blood:	n/a	n/a
6	BATF	chr8:47742166-47742315	GM12878	blood:	n/a	n/a
7	BATF	chr8:47741055-47741204	GM12878	blood:	n/a	n/a
8	BATF	chr8:47742552-47742702	GM12878	blood:	n/a	n/a
9	BCL11A	chr8:47741045-47741214	GM12878	blood:	n/a	n/a
10	BCL11A	chr8:47742173-47742308	GM12878	blood:	n/a	n/a
11	BCL11A	chr8:47742011-47742327	GM12878	blood:	n/a	n/a
12	BCL11A	chr8:47741063-47741196	GM12878	blood:	n/a	n/a
13	BCL11A	chr8:47742493-47742715	GM12878	blood:	n/a	n/a
14	BCL11A	chr8:47742558-47742696	GM12878	blood:	n/a	n/a
15	BHLHE40	chr8:47741043-47741216	HepG2	liver:	n/a	n/a
16	BHLHE40	chr8:47741998-47742438	HepG2	liver:	n/a	n/a
17	BHLHE40	chr8:47742538-47742866	HepG2	liver:	n/a	n/a
18	CEBPB	chr8:47728521-47729026	HepG2	liver:	n/a	n/a
19	CEBPB	chr8:47771800-47772967	A549	lung:	n/a	chr8:47771968-47771977 chr8:47771966-47771979 chr8:47771966-47771977 chr8:47771968-47771977 chr8:47771966-47771977 chr8:47771968-47771977 chr8:47771967-47771978 chr8:47771966-47771979 chr8:47771966-47771979 chr8:47771968-47771977
20	CEBPB	chr8:47760261-47760601	IMR90	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	chr8:47726092-47726550	MCF-7	breast:	n/a	n/a
22	CEBPB	chr8:47750993-47751208	A549	lung:	n/a	chr8:47751033-47751044
23	CEBPB	chr8:47795424-47795900	A549	lung:	n/a	chr8:47795727-47795738
24	CEBPB	chr8:47750868-47751216	HepG2	liver:	n/a	chr8:47751033-47751044
25	CEBPB	chr8:47767862-47768307	A549	lung:	n/a	n/a
26	CEBPB	chr8:47795559-47795889	HepG2	liver:	n/a	chr8:47795727-47795738
27	CEBPB	chr8:47771804-47772479	IMR90	lung:	n/a	chr8:47771968-47771977 chr8:47771966-47771979 chr8:47771966-47771977 chr8:47771968-47771977 chr8:47771966-47771977 chr8:47771968-47771977 chr8:47771967-47771978 chr8:47771966-47771979 chr8:47771966-47771979 chr8:47771968-47771977
28	CEBPB	chr8:47754786-47755004	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr8:47767015-47767397	IMR90	lung:	n/a	chr8:47767152-47767163
30	CEBPB	chr8:47728857-47729192	A549	lung:	n/a	n/a
31	CEBPB	chr8:47729582-47729782	IMR90	lung:	n/a	chr8:47729734-47729745
32	CEBPB	chr8:47786062-47786123	A549	lung:	n/a	n/a
33	CEBPB	chr8:47737694-47737724	HepG2	liver:	n/a	n/a
34	CEBPB	chr8:47755769-47755984	A549	lung:	n/a	n/a
35	CEBPB	chr8:47773617-47773955	IMR90	lung:	n/a	n/a
36	CEBPB	chr8:47726122-47726673	Hela-S3	cervix:	n/a	n/a
37	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
38	CEBPB	chr8:47766223-47766564	HepG2	liver:	n/a	chr8:47766390-47766401
39	CEBPB	chr8:47729741-47729838	HepG2	liver:	n/a	n/a
40	CEBPB	chr8:47726154-47726589	A549	lung:	n/a	n/a
41	CEBPB	chr8:47771800-47772449	HepG2	liver:	n/a	chr8:47771968-47771977 chr8:47771966-47771979 chr8:47771966-47771977 chr8:47771968-47771977 chr8:47771966-47771977 chr8:47771968-47771977 chr8:47771967-47771978 chr8:47771966-47771979 chr8:47771966-47771979 chr8:47771968-47771977
42	CEBPB	chr8:47731371-47731837	HepG2	liver:	n/a	n/a
43	CEBPB	chr8:47752678-47752878	K562	blood:	n/a	n/a
44	CEBPB	chr8:47752270-47752699	IMR90	lung:	n/a	n/a
45	CEBPB	chr8:47735917-47736098	HepG2	liver:	n/a	n/a
46	CEBPB	chr8:47726150-47726880	HepG2	liver:	n/a	n/a
47	CEBPB	chr8:47766213-47766559	IMR90	lung:	n/a	chr8:47766390-47766401
48	CEBPB	chr8:47767029-47767606	A549	lung:	n/a	chr8:47767152-47767163
49	CEBPB	chr8:47733759-47733964	A549	lung:	n/a	n/a
50	CEBPB	chr8:47732060-47732380	MCF-7	breast:	n/a	chr8:47732251-47732262

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:47751494-47751544	HRCEpiC	kidney:	n/a
2	chr8:47751623-47751673	ovcar-3	ovarian:	n/a
3	chr8:47748435-47748485	ECC-1	luminal epithelium:	n/a
4	chr8:47751494-47751544	HL-60	blood:	n/a
5	chr8:47748435-47748485	H1-hESC	embryonic stem cell:	embryo
6	chr8:47751494-47751544	AoSMC	blood vessel:	n/a
7	chr8:47761906-47761956	IMR90	lung:	fetal
8	chr8:47751494-47751544	PANC-1	pancreas:	n/a
9	chr8:47751494-47751544	HEEpiC	esophagus:	n/a
10	chr8:47751623-47751673	HIPEpiC	eye:	n/a
11	chr8:47748435-47748485	K562	blood:	n/a
12	chr8:47751953-47752003	T-47D	breast:	n/a
13	chr8:47751494-47751544	RPTEC	kidney:	n/a
14	chr8:47751623-47751673	A549	lung:	n/a
15	chr8:47751623-47751673	HL-60	blood:	n/a
16	chr8:47751623-47751673	HUVEC	blood vessel:	n/a
17	chr8:47751623-47751673	BJ	skin:	n/a
18	chr8:47761906-47761956	GM12878	blood:	n/a
19	chr8:47751494-47751544	HPAEpiC	pulmonary alveolar:	n/a
20	chr8:47761906-47761956	Jurkat	blood:	n/a
21	chr8:47751623-47751673	SK-N-SH_RA	brain:	n/a
22	chr8:47761906-47761956	AG04449	skin:	fetal
23	chr8:47751953-47752003	HepG2	liver:	n/a
24	chr8:47748435-47748485	HEK293	kidney:	embryo
25	chr8:47751953-47752003	GM19239	blood:	n/a
26	chr8:47748435-47748485	SKMC	muscle:	n/a
27	chr8:47761906-47761956	SK-N-SH_RA	brain:	n/a
28	chr8:47751953-47752003	HRE	kidney:	n/a
29	chr8:47751623-47751673	SKMC	muscle:	n/a
30	chr8:47751494-47751544	GM12891	blood:	n/a
31	chr8:47751494-47751544	Caco-2	colon:	n/a
32	chr8:47751494-47751544	AG09319	gingival:	n/a
33	chr8:47748435-47748485	HMEC	breast:	n/a
34	chr8:47751953-47752003	SK-N-SH_RA	brain:	n/a
35	chr8:47761906-47761956	NB4	blood:	n/a
36	chr8:47751953-47752003	PANC-1	pancreas:	n/a
37	chr8:47751953-47752003	U87	brain:	n/a
38	chr8:47751953-47752003	AG10803	skin:	n/a
39	chr8:47751953-47752003	Jurkat	blood:	n/a
40	chr8:47748435-47748485	AG09319	gingival:	n/a
41	chr8:47751953-47752003	AoSMC	blood vessel:	n/a
42	chr8:47761906-47761956	SK-N-MC	brain:	n/a
43	chr8:47748435-47748485	HCPEpiC	choroid plexus:	n/a
44	chr8:47751494-47751544	SK-N-SH_RA	brain:	n/a
45	chr8:47751494-47751544	AG09309	skin:	n/a
46	chr8:47751494-47751544	PFSK-1	brain:	n/a
47	chr8:47751953-47752003	A549	lung:	n/a
48	chr8:47761906-47761956	RPTEC	kidney:	n/a
49	chr8:47761906-47761956	BE2_C	brain:	n/a
50	chr8:47751623-47751673	HPAEpiC	pulmonary alveolar:	n/a

No data

(count:85 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-1134I14.8.1-3	chr8:47765729-47765991	NONHSAT126421
2	lnc-RP11-1134I14.8.1-3	chr8:47759598-47759631	ENSG00000253314.1
3	lnc-RP11-1134I14.8.1-3	chr8:47760896-47761152	NONHSAT126423
4	lnc-RP11-1134I14.8.1-3	chr8:47753899-47753974	NONHSAT126420
5	lnc-RP11-1134I14.8.1-3	chr8:47748371-47748420	NONHSAT126415
6	lnc-RP11-1134I14.8.1-3	chr8:47752486-47752557	NONHSAT126419
7	lnc-RP11-1134I14.8.1-3	chr8:47754972-47755048	NONHSAT126419
8	lnc-RP11-1134I14.8.1-3	chr8:47752508-47752557	NONHSAT126420
9	lnc-RP11-1134I14.8.1-3	chr8:47762290-47762365	NR_027013
10	lnc-RP11-1134I14.8.1-3	chr8:47754972-47755048	NONHSAT126421
11	lnc-RP11-1134I14.8.1-3	chr8:47766092-47766216	NONHSAT126424
12	lnc-RP11-1134I14.8.1-3	chr8:47761071-47761152	ENSG00000253314.1
13	lnc-RP11-1134I14.8.1-3	chr8:47752667-47752748	ENSG00000253314.1
14	lnc-RP11-1134I14.8.1-3	chr8:47757651-47757703	ENSG00000253314.1
15	lnc-RP11-1134I14.8.1-3	chr8:47762290-47762365	ENSG00000253314.1
16	lnc-RP11-1134I14.8.1-3	chr8:47759598-47759722	NONHSAT126415
17	lnc-RP11-1134I14.8.1-3	chr8:47766386-47767407	NONHSAT126421
18	lnc-RP11-1134I14.8.1-3	chr8:47752438-47752557	ENSG00000253314.1
19	lnc-RP11-1134I14.8.1-3	chr8:47752667-47752748	ENSG00000253314.1
20	lnc-RP11-1134I14.8.1-3	chr8:47754972-47755048	NONHSAT126415
21	lnc-RP11-1134I14.8.1-3	chr8:47760406-47761152	NR_027013
22	lnc-RP11-1134I14.8.1-3	chr8:47752667-47752748	ENSG00000253314.1
23	lnc-RP11-1134I14.8.1-3	chr8:47753899-47753974	NR_027013
24	lnc-RP11-1134I14.8.1-3	chr8:47752667-47752748	ENSG00000253314.1
25	lnc-RP11-1134I14.8.1-3	chr8:47759598-47759722	NR_027013
26	lnc-RP11-1134I14.8.1-3	chr8:47765729-47765991	NONHSAT126424
27	lnc-RP11-1134I14.8.1-3	chr8:47759598-47759722	NONHSAT126419
28	lnc-RP11-1134I14.8.1-3	chr8:47759598-47759722	NONHSAT126421
29	lnc-RP11-1134I14.8.1-3	chr8:47752667-47752748	NONHSAT126415
30	lnc-RP11-1134I14.8.1-3	chr8:47762290-47762365	NONHSAT126421
31	lnc-RP11-350F16.2.1-5	chr8:47738850-47740031	NONHSAT126413
32	lnc-RP11-1134I14.8.1-3	chr8:47754972-47755048	ENSG00000253314.1
33	lnc-RP11-1134I14.8.1-3	chr8:47748364-47748420	ENSG00000253314.1
34	lnc-RP11-1134I14.8.1-3	chr8:47752667-47752748	NONHSAT126420
35	lnc-RP11-1134I14.8.1-3	chr8:47753899-47753974	ENSG00000253314.1
36	lnc-RP11-350F16.2.1-4	chr8:47749200-47750328	NONHSAT126416
37	lnc-RP11-1134I14.8.1-3	chr8:47733859-47734050	ENSG00000253314.1
38	lnc-RP11-1134I14.8.1-3	chr8:47754972-47755048	NONHSAT126420
39	lnc-RP11-1134I14.8.1-3	chr8:47754972-47755048	NR_027013
40	lnc-RP11-1134I14.8.1-3	chr8:47752667-47752748	NONHSAT126419
41	lnc-RP11-1134I14.8.1-3	chr8:47765729-47765833	ENSG00000253314.1
42	lnc-RP11-350F16.2.1-2	chr8:47722340-47723308	XLOC_007078
43	lnc-RP11-1134I14.8.1-3	chr8:47759598-47759688	ENSG00000253314.1
44	lnc-RP11-1134I14.8.1-3	chr8:47757651-47757703	ENSG00000253314.1
45	lnc-RP11-1134I14.8.1-3	chr8:47752667-47752748	NR_027013
46	lnc-RP11-1134I14.8.1-3	chr8:47752508-47752557	NONHSAT126421
47	lnc-RP11-1134I14.8.1-3	chr8:47766092-47766220	NONHSAT126423
48	lnc-RP11-1134I14.8.1-3	chr8:47754972-47755048	ENSG00000253314.1
49	lnc-RP11-1134I14.8.1-3	chr8:47754972-47755048	ENSG00000253314.1
50	lnc-RP11-1134I14.8.1-3	chr8:47755811-47755918	ENSG00000253314.1

No data

Variant related genes	Relation type
MTND1P7	TF binding region
ENSG00000253803	TF binding region
MTND6P20	TF binding region
LINC00293	TF binding region
RNU6-656P	TF binding region
ENSG00000254118	TF binding region
MTND1P7	CpG island
ENSG00000253803	CpG island
MTND6P20	CpG island
LINC00293	CpG island
RNU6-656P	CpG island
ENSG00000254118	CpG island
PPARGC1A	miRNA target sites
USO1	miRNA target sites

Extended variants
information (count: 1256 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:1256 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190210640	chr8:47722406-47722407	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs546976909	chr8:47722437-47722438	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs565283398	chr8:47722463-47722464	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs532649081	chr8:47722465-47722466	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs551135710	chr8:47722478-47722479	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs569416538	chr8:47722488-47722489	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs34449615	chr8:47722504-47722505	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs371651659	chr8:47722510-47722511	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs548783528	chr8:47722552-47722553	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs567016951	chr8:47722624-47722625	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs182766504	chr8:47722703-47722704	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs527276040	chr8:47722794-47722795	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs552503183	chr8:47722798-47722799	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs12543892	chr8:47722829-47722830	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs538334684	chr8:47722834-47722835	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs556668069	chr8:47722836-47722837	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs575321287	chr8:47722844-47722845	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs549233662	chr8:47722845-47722846	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs542425324	chr8:47722869-47722870	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs573008069	chr8:47722874-47722875	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs570747032	chr8:47722875-47722876	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs146980700	chr8:47722883-47722884	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
23	rs565268855	chr8:47722893-47722894	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs369349149	chr8:47722897-47722898	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
25	rs138143415	chr8:47722908-47722909	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
26	rs375145138	chr8:47722912-47722913	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
27	rs528109907	chr8:47722953-47722954	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs186119375	chr8:47722956-47722957	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
29	rs530226107	chr8:47722985-47722986	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
30	rs548451967	chr8:47723004-47723005	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
31	rs192284083	chr8:47723024-47723025	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
32	rs527972926	chr8:47723041-47723042	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
33	rs552488958	chr8:47723104-47723105	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
34	rs115928448	chr8:47723128-47723129	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
35	rs538220566	chr8:47723161-47723162	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
36	rs371651855	chr8:47723165-47723166	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
37	rs556934215	chr8:47723175-47723176	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
38	rs183650493	chr8:47723238-47723239	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
39	rs536351459	chr8:47723244-47723245	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
40	rs535283775	chr8:47723245-47723246	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
41	rs554463827	chr8:47723275-47723276	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
42	rs145094969	chr8:47728909-47728910	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs551192973	chr8:47728913-47728914	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs566786967	chr8:47728948-47728949	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs191009018	chr8:47728957-47728958	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs551452903	chr8:47728978-47728979	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs150959937	chr8:47728985-47728986	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs375655009	chr8:47728991-47728992	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs181763922	chr8:47729010-47729011	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs140804952	chr8:47729085-47729086	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:81)

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
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:17 , 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
16	chr8:47767400-47767800	Enhancers	Placenta	Placenta
17	chr8:47780000-47781800	ZNF genes & repeats	Adipose Nuclei	Adipose

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