Variant report

Variant	nsv6177
Chromosome Location	chr8:47840361-47884867
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:47868491-47869037	HepG2	liver:	n/a	n/a
2	ATF1	chr8:47868616-47868941	K562	blood:	n/a	n/a
3	BHLHE40	chr8:47868720-47869144	HepG2	liver:	n/a	n/a
4	BHLHE40	chr8:47867816-47869101	GM12878	blood:	n/a	n/a
5	CEBPB	chr8:47842143-47842310	HepG2	liver:	n/a	chr8:47842227-47842238
6	CEBPB	chr8:47883507-47883648	K562	blood:	n/a	chr8:47883570-47883587
7	CEBPB	chr8:47875291-47875419	HepG2	liver:	n/a	chr8:47875329-47875340
8	CEBPB	chr8:47865186-47865625	HepG2	liver:	n/a	chr8:47865596-47865607 chr8:47865340-47865351
9	CEBPB	chr8:47865179-47865508	A549	lung:	n/a	chr8:47865340-47865351
10	CEBPB	chr8:47851601-47851855	K562	blood:	n/a	n/a
11	CEBPB	chr8:47865172-47865508	IMR90	lung:	n/a	chr8:47865340-47865351
12	CEBPB	chr8:47865251-47865672	K562	blood:	n/a	chr8:47865596-47865607 chr8:47865340-47865351
13	CHD1	chr8:47868127-47868870	GM12878	blood:	n/a	n/a
14	CHD2	chr8:47868536-47869077	GM12878	blood:	n/a	n/a
15	CHD2	chr8:47867790-47868119	GM12878	blood:	n/a	n/a
16	CTCF	chr8:47868720-47868870	HMF	breast:	n/a	chr8:47868749-47868759 chr8:47868747-47868763 chr8:47868746-47868764 chr8:47868741-47868762 chr8:47868748-47868761 chr8:47868752-47868761
17	CTCF	chr8:47868740-47868890	GM12874	blood:	n/a	chr8:47868749-47868759 chr8:47868747-47868763 chr8:47868746-47868764 chr8:47868741-47868762 chr8:47868748-47868761 chr8:47868752-47868761
18	CTCF	chr8:47868720-47868870	K562	blood:	n/a	chr8:47868749-47868759 chr8:47868747-47868763 chr8:47868746-47868764 chr8:47868741-47868762 chr8:47868748-47868761 chr8:47868752-47868761
19	CTCF	chr8:47868619-47869034	Spleen_OC	spleen:	n/a	chr8:47868749-47868759 chr8:47868747-47868763 chr8:47868746-47868764 chr8:47868741-47868762 chr8:47868748-47868761 chr8:47868876-47868894 chr8:47868752-47868761
20	CTCF	chr8:47868680-47868830	HL-60	blood:	n/a	chr8:47868749-47868759 chr8:47868747-47868763 chr8:47868746-47868764 chr8:47868741-47868762 chr8:47868748-47868761 chr8:47868752-47868761
21	CTCF	chr8:47868640-47868790	HAc	cerebellar:	n/a	chr8:47868749-47868759 chr8:47868747-47868763 chr8:47868746-47868764 chr8:47868741-47868762 chr8:47868748-47868761 chr8:47868752-47868761
22	CTCF	chr8:47868510-47869082	HepG2	liver:	n/a	chr8:47868749-47868759 chr8:47868747-47868763 chr8:47868746-47868764 chr8:47868741-47868762 chr8:47868748-47868761 chr8:47868876-47868894 chr8:47868752-47868761
23	CTCF	chr8:47868740-47868890	AG09319	gingival:	n/a	chr8:47868749-47868759 chr8:47868747-47868763 chr8:47868746-47868764 chr8:47868741-47868762 chr8:47868748-47868761 chr8:47868752-47868761
24	CTCF	chr8:47868740-47868890	HEK293	kidney:	n/a	chr8:47868749-47868759 chr8:47868747-47868763 chr8:47868746-47868764 chr8:47868741-47868762 chr8:47868748-47868761 chr8:47868752-47868761
25	CTCF	chr8:47868537-47869088	K562	blood:	n/a	chr8:47868749-47868759 chr8:47868747-47868763 chr8:47868746-47868764 chr8:47868741-47868762 chr8:47868748-47868761 chr8:47868876-47868894 chr8:47868752-47868761
26	CTCF	chr8:47868680-47868830	HEEpiC	esophagus:	n/a	chr8:47868749-47868759 chr8:47868747-47868763 chr8:47868746-47868764 chr8:47868741-47868762 chr8:47868748-47868761 chr8:47868752-47868761
27	CTCF	chr8:47868620-47869105	Gliobla	brain:	n/a	chr8:47868749-47868759 chr8:47868747-47868763 chr8:47868746-47868764 chr8:47868741-47868762 chr8:47868748-47868761 chr8:47868876-47868894 chr8:47868752-47868761
28	CTCF	chr8:47868740-47868890	BJ	skin:	n/a	chr8:47868749-47868759 chr8:47868747-47868763 chr8:47868746-47868764 chr8:47868741-47868762 chr8:47868748-47868761 chr8:47868752-47868761
29	CTCF	chr8:47868458-47869105	GM12878	blood:	n/a	chr8:47868749-47868759 chr8:47868747-47868763 chr8:47868746-47868764 chr8:47868741-47868762 chr8:47868748-47868761 chr8:47868876-47868894 chr8:47868752-47868761
30	CTCF	chr8:47868624-47868893	GM12891	blood:	n/a	chr8:47868749-47868759 chr8:47868747-47868763 chr8:47868746-47868764 chr8:47868741-47868762 chr8:47868748-47868761 chr8:47868752-47868761
31	CTCF	chr8:47868720-47868870	AoAF	blood vessel:	n/a	chr8:47868749-47868759 chr8:47868747-47868763 chr8:47868746-47868764 chr8:47868741-47868762 chr8:47868748-47868761 chr8:47868752-47868761
32	CTCF	chr8:47868720-47868870	HMEC	breast:	n/a	chr8:47868749-47868759 chr8:47868747-47868763 chr8:47868746-47868764 chr8:47868741-47868762 chr8:47868748-47868761 chr8:47868752-47868761
33	CTCF	chr8:47868648-47869003	HepG2	liver:	n/a	chr8:47868749-47868759 chr8:47868747-47868763 chr8:47868746-47868764 chr8:47868741-47868762 chr8:47868748-47868761 chr8:47868876-47868894 chr8:47868752-47868761
34	CTCF	chr8:47868740-47868890	GM12801	blood:	n/a	chr8:47868749-47868759 chr8:47868747-47868763 chr8:47868746-47868764 chr8:47868741-47868762 chr8:47868748-47868761 chr8:47868752-47868761
35	CTCF	chr8:47868555-47869138	IMR90	lung:	n/a	chr8:47868749-47868759 chr8:47868747-47868763 chr8:47868746-47868764 chr8:47868741-47868762 chr8:47868748-47868761 chr8:47868876-47868894 chr8:47868752-47868761
36	CTCF	chr8:47868602-47869006	ECC-1	luminal epithelium:	n/a	chr8:47868749-47868759 chr8:47868747-47868763 chr8:47868746-47868764 chr8:47868741-47868762 chr8:47868748-47868761 chr8:47868876-47868894 chr8:47868752-47868761
37	CTCF	chr8:47868720-47868870	HCM	heart:	n/a	chr8:47868749-47868759 chr8:47868747-47868763 chr8:47868746-47868764 chr8:47868741-47868762 chr8:47868748-47868761 chr8:47868752-47868761
38	CTCF	chr8:47868655-47869093	GM20000	blood:	n/a	chr8:47868749-47868759 chr8:47868747-47868763 chr8:47868746-47868764 chr8:47868741-47868762 chr8:47868748-47868761 chr8:47868876-47868894 chr8:47868752-47868761
39	CTCF	chr8:47868700-47868850	GM12864	blood:	n/a	chr8:47868749-47868759 chr8:47868747-47868763 chr8:47868746-47868764 chr8:47868741-47868762 chr8:47868748-47868761 chr8:47868752-47868761
40	CTCF	chr8:47873880-47874030	SAEC	small airway:	n/a	n/a
41	CTCF	chr8:47868740-47868890	HAc	cerebellar:	n/a	chr8:47868749-47868759 chr8:47868747-47868763 chr8:47868746-47868764 chr8:47868741-47868762 chr8:47868748-47868761 chr8:47868752-47868761
42	CTCF	chr8:47868680-47868830	HRPEpiC	eye:	n/a	chr8:47868749-47868759 chr8:47868747-47868763 chr8:47868746-47868764 chr8:47868741-47868762 chr8:47868748-47868761 chr8:47868752-47868761
43	CTCF	chr8:47868720-47868870	MCF-7	breast:	n/a	chr8:47868749-47868759 chr8:47868747-47868763 chr8:47868746-47868764 chr8:47868741-47868762 chr8:47868748-47868761 chr8:47868752-47868761
44	CTCF	chr8:47868720-47868870	HPF	lung:	n/a	chr8:47868749-47868759 chr8:47868747-47868763 chr8:47868746-47868764 chr8:47868741-47868762 chr8:47868748-47868761 chr8:47868752-47868761
45	CTCF	chr8:47868628-47868947	Lung_OC	lung:	n/a	chr8:47868749-47868759 chr8:47868747-47868763 chr8:47868746-47868764 chr8:47868741-47868762 chr8:47868748-47868761 chr8:47868876-47868894 chr8:47868752-47868761
46	CTCF	chr8:47850935-47851014	Fibrobl	skin:	n/a	n/a
47	CTCF	chr8:47865137-47865170	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr8:47868642-47868976	Medullo	brain:	n/a	chr8:47868749-47868759 chr8:47868747-47868763 chr8:47868746-47868764 chr8:47868741-47868762 chr8:47868748-47868761 chr8:47868876-47868894 chr8:47868752-47868761
49	CTCF	chr8:47868625-47869005	A549	lung:	n/a	chr8:47868749-47868759 chr8:47868747-47868763 chr8:47868746-47868764 chr8:47868741-47868762 chr8:47868748-47868761 chr8:47868876-47868894 chr8:47868752-47868761
50	CTCF	chr8:47868260-47868410	GM12875	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:47867238-47867288	HCF	heart:	n/a
2	chr8:47867238-47867288	HCF	heart:	n/a
3	chr8:47862954-47863004	GM19239	blood:	n/a
4	chr8:47866784-47866834	AG09309	skin:	n/a
5	chr8:47866659-47866709	HepG2	liver:	n/a
6	chr8:47869097-47869147	MCF10A-Er-Src	breast:	n/a
7	chr8:47862954-47863004	Caco-2	colon:	n/a
8	chr8:47869097-47869147	BE2_C	brain:	n/a
9	chr8:47862954-47863004	H1-hESC	embryonic stem cell:	embryo
10	chr8:47867238-47867288	HPAEpiC	pulmonary alveolar:	n/a
11	chr8:47862954-47863004	RPTEC	kidney:	n/a
12	chr8:47867238-47867288	GM06990	blood:	n/a
13	chr8:47867238-47867288	RPTEC	kidney:	n/a
14	chr8:47866784-47866834	NB4	blood:	n/a
15	chr8:47866183-47866233	HUVEC	blood vessel:	n/a
16	chr8:47866659-47866709	HAEpiC	amniotic membrane:	n/a
17	chr8:47862954-47863004	ECC-1	luminal epithelium:	n/a
18	chr8:47866784-47866834	RPTEC	kidney:	n/a
19	chr8:47869097-47869147	A549	lung:	n/a
20	chr8:47866183-47866233	HL-60	blood:	n/a
21	chr8:47862954-47863004	NHBE	bronchial:	n/a
22	chr8:47869097-47869147	GM06990	blood:	n/a
23	chr8:47866659-47866709	ovcar-3	ovarian:	n/a
24	chr8:47866659-47866709	PANC-1	pancreas:	n/a
25	chr8:47869097-47869147	BJ	skin:	n/a
26	chr8:47862954-47863004	NHDF-neo	bronchial:	n/a
27	chr8:47867238-47867288	Hepatocyte	liver:	n/a
28	chr8:47866784-47866834	SKMC	muscle:	n/a
29	chr8:47866183-47866233	K562	blood:	n/a
30	chr8:47866784-47866834	GM19239	blood:	n/a
31	chr8:47866183-47866233	T-47D	breast:	n/a
32	chr8:47866784-47866834	AG04449	skin:	fetal
33	chr8:47862954-47863004	AG10803	skin:	n/a
34	chr8:47867238-47867288	HRPEpiC	eye:	n/a
35	chr8:47866659-47866709	HCT-116	colon:	n/a
36	chr8:47867238-47867288	Caco-2	colon:	n/a
37	chr8:47866659-47866709	HUVEC	blood vessel:	n/a
38	chr8:47869097-47869147	Hela-S3	cervix:	n/a
39	chr8:47866183-47866233	NHDF-neo	bronchial:	n/a
40	chr8:47866784-47866834	HCF	heart:	n/a
41	chr8:47869097-47869147	ProgFib	skin:	n/a
42	chr8:47867238-47867288	NHBE	bronchial:	n/a
43	chr8:47867238-47867288	AG09319	gingival:	n/a
44	chr8:47866183-47866233	U87	brain:	n/a
45	chr8:47866659-47866709	LNCaP	prostate:	n/a
46	chr8:47862954-47863004	HUVEC	blood vessel:	n/a
47	chr8:47869097-47869147	AoSMC	blood vessel:	n/a
48	chr8:47869097-47869147	AG10803	skin:	n/a
49	chr8:47862954-47863004	GM12878	blood:	n/a
50	chr8:47862954-47863004	HCM	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:47827930..47831126-chr8:47870805..47874048,3	K562	blood:
2	chr8:47868490..47869263-chr8:48105434..48106345,3	MCF-7	breast:
3	chr8:47868367..47869450-chr8:47955570..47956475,5	MCF-7	breast:
4	chr8:47828970..47829945-chr8:47868388..47869115,3	MCF-7	breast:
5	chr8:47829182..47829917-chr8:47868447..47869168,4	MCF-7	breast:
6	chr8:47868349..47869331-chr8:48105662..48106730,3	MCF-7	breast:
7	chr8:47868405..47869388-chr8:48173018..48173532,2	K562	blood:
8	chr8:47868480..47869132-chr8:48100099..48100692,2	MCF-7	breast:
9	chr8:47868355..47869368-chr8:48078653..48079520,3	MCF-7	breast:
10	chr8:47848954..47851708-chr8:48172110..48173812,2	MCF-7	breast:
11	chr8:47868712..47869324-chr8:48091494..48092220,2	K562	blood:
12	chr8:47864214..47867123-chr8:47867478..47869863,2	K562	blood:
13	chr8:47827930..47830534-chr8:47872091..47874048,2	K562	blood:
14	chr8:47864214..47867123-chr8:47867478..47869863,2	K562	blood:
15	chr8:47619331..47620431-chr8:47868217..47869326,4	MCF-7	breast:
16	chr8:47868390..47869335-chr8:48103589..48104192,2	MCF-7	breast:
17	chr8:47619541..47620262-chr8:47868295..47869178,3	MCF-7	breast:
18	chr8:47618289..47619061-chr8:47868266..47869014,2	MCF-7	breast:
19	chr8:46940536..46941325-chr8:47868294..47869211,2	K562	blood:
20	chr8:47829086..47829943-chr8:47868391..47869236,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-350F16.2.1-3	chr8:47862330-47862558	NONHSAT126427
2	lnc-RP11-350F16.2.1-1	chr8:47849800-47849870	l_3587_chr8:47841497-47849870_testes
3	lnc-RP11-350F16.2.1-1	chr8:47842462-47842535	ENSG00000253782.1
4	lnc-RP11-350F16.2.1-1	chr8:47841498-47842473	l_3587_chr8:47841497-47849870_testes
5	lnc-LINC00293-1	chr8:47840258-47840454	ENSG00000253745.1
6	lnc-RP11-350F16.2.1-1	chr8:47842942-47843058	ENSG00000253782.1
7	lnc-RP11-350F16.2.1-1	chr8:47845800-47846068	ENSG00000253782.1
8	lnc-RP11-350F16.2.1-3	chr8:47863285-47863520	NONHSAT126427

Variant related genes	Relation type
ENSG00000253782	TF binding region
ENSG00000253782	CpG island
ENSG00000253502	chromatin interactions
ENSG00000164808	chromatin interactions

Extended variants
information (count: 1065 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:1065 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs35072815	chr8:47840362-47840363	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
2	rs544319618	chr8:47840372-47840373	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
3	rs562705115	chr8:47840387-47840388	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
4	rs530265056	chr8:47840396-47840397	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
5	rs377210289	chr8:47840418-47840419	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
6	rs193062162	chr8:47840461-47840462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs184855053	chr8:47840471-47840472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs73578921	chr8:47840476-47840477	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs189700122	chr8:47840492-47840493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs528009896	chr8:47840498-47840499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs571158632	chr8:47840500-47840501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs538709459	chr8:47840557-47840558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs557108138	chr8:47840571-47840572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs114879116	chr8:47840595-47840596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs547647466	chr8:47840610-47840611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs570730412	chr8:47840617-47840618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs539595590	chr8:47840721-47840722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs117753213	chr8:47840732-47840733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs554566003	chr8:47840775-47840776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs6984976	chr8:47840781-47840782	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs537941989	chr8:47840800-47840801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs554296093	chr8:47840814-47840815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs116008563	chr8:47840849-47840850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs144063977	chr8:47840871-47840872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs147326649	chr8:47840899-47840900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs113630863	chr8:47840906-47840907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs116639951	chr8:47840932-47840933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs530227489	chr8:47840937-47840938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs137863693	chr8:47840953-47840954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs560531617	chr8:47840964-47840965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs574358899	chr8:47840975-47840976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs143408194	chr8:47840984-47840985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs552616897	chr8:47841000-47841001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs35836001	chr8:47841049-47841050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs150517348	chr8:47841146-47841147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs373097414	chr8:47841147-47841148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs35125913	chr8:47841168-47841169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs192345863	chr8:47841193-47841194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs534096219	chr8:47841204-47841205	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs550676937	chr8:47841208-47841209	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs569022436	chr8:47841233-47841234	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs139507662	chr8:47841284-47841285	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs114355735	chr8:47841305-47841306	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs566569722	chr8:47841306-47841307	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs376416517	chr8:47841417-47841418	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs577115922	chr8:47841418-47841419	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs78551923	chr8:47841485-47841486	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs28508163	chr8:47841634-47841635	ZNF genes & repeats Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs576804062	chr8:47841655-47841656	ZNF genes & repeats Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
50	rs149697234	chr8:47841720-47841721	ZNF genes & repeats Weak transcription Enhancers	lncRNA	n/a	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
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
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
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
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:56 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:47838200-47841600	Weak transcription	Spleen	Spleen
2	chr8:47838800-47847000	Weak transcription	Gastric	stomach
3	chr8:47841200-47845600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
4	chr8:47841600-47842000	Enhancers	Spleen	Spleen
5	chr8:47842000-47844200	Weak transcription	Spleen	Spleen
6	chr8:47844200-47845200	Genic enhancers	Spleen	Spleen
7	chr8:47844200-47845400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr8:47845200-47847000	Weak transcription	Spleen	Spleen
9	chr8:47846800-47850200	Enhancers	Primary B cells from peripheral blood	blood
10	chr8:47847000-47847200	Enhancers	Spleen	Spleen
11	chr8:47851600-47852200	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr8:47851600-47853200	Enhancers	Primary B cells from peripheral blood	blood
13	chr8:47863000-47867800	Enhancers	Primary B cells from peripheral blood	blood
14	chr8:47864400-47865400	Enhancers	Primary B cells from cord blood	blood
15	chr8:47864600-47865400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
16	chr8:47865000-47865200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr8:47865000-47865200	Enhancers	Spleen	Spleen
18	chr8:47867000-47869200	Enhancers	Primary B cells from cord blood	blood
19	chr8:47867200-47867800	Enhancers	GM12878-XiMat	blood
20	chr8:47867200-47868600	Enhancers	Monocytes-CD14+_RO01746	blood
21	chr8:47867200-47869000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
22	chr8:47867200-47869200	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr8:47867400-47867600	Enhancers	Spleen	Spleen
24	chr8:47867400-47868600	Enhancers	Adipose Nuclei	Adipose
25	chr8:47867400-47869000	Enhancers	Primary monocytes fromperipheralblood	blood
26	chr8:47867600-47871800	Weak transcription	Fetal Heart	heart
27	chr8:47867600-47872600	Weak transcription	Spleen	Spleen
28	chr8:47867800-47868000	Flanking Active TSS	Primary B cells from peripheral blood	blood
29	chr8:47867800-47868600	Flanking Active TSS	GM12878-XiMat	blood
30	chr8:47868000-47868200	Enhancers	Primary B cells from peripheral blood	blood
31	chr8:47868000-47869200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
32	chr8:47868200-47868400	Flanking Active TSS	Primary B cells from peripheral blood	blood
33	chr8:47868200-47868800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr8:47868200-47869000	Enhancers	Primary T helper cells PMA-I stimulated	--
35	chr8:47868200-47869000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
36	chr8:47868200-47869000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
37	chr8:47868400-47868800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
38	chr8:47868400-47868800	Enhancers	Primary T helper cells fromperipheralblood	blood
39	chr8:47868400-47868800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
40	chr8:47868400-47869000	Enhancers	Primary T helper naive cells from peripheral blood	blood
41	chr8:47868400-47869200	Enhancers	Primary B cells from peripheral blood	blood
42	chr8:47868600-47869000	Enhancers	Brain Substantia Nigra	brain
43	chr8:47868600-47869200	Enhancers	GM12878-XiMat	blood
44	chr8:47869200-47872600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
45	chr8:47871000-47871400	Enhancers	Placenta	Placenta
46	chr8:47871400-47873000	Weak transcription	Placenta	Placenta
47	chr8:47872600-47873800	Enhancers	Spleen	Spleen
48	chr8:47872600-47875800	Enhancers	Breast Myoepithelial Primary Cells	Breast
49	chr8:47872800-47874800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr8:47873000-47875200	Enhancers	Placenta	Placenta

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