Variant report

Variant	nsv1024217
Chromosome Location	chr8:9046230-9062514
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	chr8:9060202-9060298	K562	blood:	n/a	n/a
2	CEBPB	chr8:9048043-9048305	HepG2	liver:	n/a	chr8:9048176-9048189 chr8:9048177-9048188
3	CEBPB	chr8:9048025-9048374	H1-hESC	embryonic stem cell:	n/a	chr8:9048176-9048189 chr8:9048177-9048188
4	CEBPB	chr8:9048013-9048350	K562	blood:	n/a	chr8:9048176-9048189 chr8:9048177-9048188
5	CEBPB	chr8:9048010-9048360	IMR90	lung:	n/a	chr8:9048176-9048189 chr8:9048177-9048188
6	CEBPB	chr8:9048040-9048343	A549	lung:	n/a	chr8:9048176-9048189 chr8:9048177-9048188
7	CEBPB	chr8:9047999-9048355	Hela-S3	cervix:	n/a	chr8:9048176-9048189 chr8:9048177-9048188
8	CEBPB	chr8:9058204-9058498	HepG2	liver:	n/a	n/a
9	CEBPB	chr8:9047136-9047376	A549	lung:	n/a	n/a
10	CEBPB	chr8:9054775-9054792	K562	blood:	n/a	n/a
11	CTCF	chr8:9060420-9060570	AoAF	blood vessel:	n/a	n/a
12	CTCF	chr8:9055300-9055450	SK-N-SH_RA	brain:	n/a	n/a
13	CUX1	chr8:9049618-9049733	K562	blood:	n/a	n/a
14	E2F4	chr8:9049323-9049428	MCF10A-Er-Src	breast:	n/a	n/a
15	E2F6	chr8:9056255-9056371	K562	blood:	n/a	n/a
16	EBF1	chr8:9047098-9047562	GM12878	blood:	n/a	chr8:9047373-9047384 chr8:9047374-9047384 chr8:9047374-9047383 chr8:9047300-9047309
17	EBF1	chr8:9047139-9047434	GM12878	blood:	n/a	chr8:9047373-9047384 chr8:9047374-9047384 chr8:9047374-9047383 chr8:9047300-9047309
18	EBF1	chr8:9047171-9047493	GM12878	blood:	n/a	chr8:9047373-9047384 chr8:9047374-9047384 chr8:9047374-9047383 chr8:9047300-9047309
19	EP300	chr8:9055236-9056115	SK-N-SH_RA	brain:	n/a	chr8:9055605-9055619
20	EP300	chr8:9055148-9055548	K562	blood:	n/a	n/a
21	EP300	chr8:9055169-9056137	SK-N-SH_RA	brain:	n/a	chr8:9055605-9055619
22	EP300	chr8:9054711-9057399	SK-N-SH	brain:	n/a	chr8:9055605-9055619
23	EP300	chr8:9047163-9047481	GM12878	blood:	n/a	n/a
24	EP300	chr8:9053775-9053828	K562	blood:	n/a	n/a
25	FOS	chr8:9048131-9048272	MCF10A-Er-Src	breast:	n/a	n/a
26	GATA2	chr8:9055213-9056127	SH-SY5Y	brain:	n/a	chr8:9055461-9055468 chr8:9055457-9055473 chr8:9055461-9055468 chr8:9055460-9055470 chr8:9055454-9055475 chr8:9055981-9055989 chr8:9055457-9055473 chr8:9055461-9055468
27	GATA3	chr8:9052290-9052642	SH-SY5Y	brain:	n/a	n/a
28	GATA3	chr8:9049377-9049698	T-47D	breast:	n/a	n/a
29	GATA3	chr8:9055158-9055732	SK-N-SH	brain:	n/a	chr8:9055461-9055468 chr8:9055457-9055473 chr8:9055461-9055468 chr8:9055460-9055470 chr8:9055454-9055475 chr8:9055457-9055473 chr8:9055461-9055468
30	GATA3	chr8:9055916-9056122	SH-SY5Y	brain:	n/a	chr8:9055981-9055989
31	GATA3	chr8:9055237-9055663	SK-N-SH	brain:	n/a	chr8:9055461-9055468 chr8:9055457-9055473 chr8:9055461-9055468 chr8:9055460-9055470 chr8:9055454-9055475 chr8:9055457-9055473 chr8:9055461-9055468
32	GATA3	chr8:9061143-9061327	SH-SY5Y	brain:	n/a	n/a
33	GATA3	chr8:9049329-9049809	MCF-7	breast:	n/a	n/a
34	GATA3	chr8:9055222-9055694	SH-SY5Y	brain:	n/a	chr8:9055461-9055468 chr8:9055457-9055473 chr8:9055461-9055468 chr8:9055460-9055470 chr8:9055454-9055475 chr8:9055457-9055473 chr8:9055461-9055468
35	GATA3	chr8:9049351-9049729	T-47D	breast:	n/a	n/a
36	IRF1	chr8:9053731-9053732	K562	blood:	n/a	n/a
37	JUN	chr8:9062269-9062469	K562	blood:	n/a	n/a
38	JUND	chr8:9055313-9055728	K562	blood:	n/a	chr8:9055470-9055479
39	MAFF	chr8:9053471-9053830	HepG2	liver:	n/a	chr8:9053645-9053659 chr8:9053646-9053664
40	MAFF	chr8:9053474-9053830	K562	blood:	n/a	chr8:9053645-9053659 chr8:9053646-9053664
41	MAFK	chr8:9047532-9047786	HepG2	liver:	n/a	chr8:9047665-9047681
42	MAFK	chr8:9053478-9053839	K562	blood:	n/a	chr8:9053652-9053663 chr8:9053644-9053660 chr8:9053647-9053662 chr8:9053652-9053663 chr8:9053645-9053659 chr8:9053647-9053663 chr8:9053642-9053662 chr8:9053651-9053662
43	MAFK	chr8:9053472-9053821	Hela-S3	cervix:	n/a	chr8:9053652-9053663 chr8:9053644-9053660 chr8:9053647-9053662 chr8:9053652-9053663 chr8:9053645-9053659 chr8:9053647-9053663 chr8:9053642-9053662 chr8:9053651-9053662
44	MAFK	chr8:9053471-9053839	HepG2	liver:	n/a	chr8:9053652-9053663 chr8:9053644-9053660 chr8:9053647-9053662 chr8:9053652-9053663 chr8:9053645-9053659 chr8:9053647-9053663 chr8:9053642-9053662 chr8:9053651-9053662
45	MAFK	chr8:9053490-9053842	H1-hESC	embryonic stem cell:	n/a	chr8:9053652-9053663 chr8:9053644-9053660 chr8:9053647-9053662 chr8:9053652-9053663 chr8:9053645-9053659 chr8:9053647-9053663 chr8:9053642-9053662 chr8:9053651-9053662
46	MAFK	chr8:9053477-9053825	HepG2	liver:	n/a	chr8:9053652-9053663 chr8:9053644-9053660 chr8:9053647-9053662 chr8:9053652-9053663 chr8:9053645-9053659 chr8:9053647-9053663 chr8:9053642-9053662 chr8:9053651-9053662
47	MAFK	chr8:9049321-9049555	HepG2	liver:	n/a	chr8:9049418-9049429 chr8:9049418-9049429
48	MAFK	chr8:9053474-9053830	IMR90	lung:	n/a	chr8:9053652-9053663 chr8:9053644-9053660 chr8:9053647-9053662 chr8:9053652-9053663 chr8:9053645-9053659 chr8:9053647-9053663 chr8:9053642-9053662 chr8:9053651-9053662
49	MAX	chr8:9056847-9057086	H1-hESC	embryonic stem cell:	n/a	chr8:9056974-9056985 chr8:9056975-9056984
50	MYC	chr8:9048271-9048552	MCF10A-Er-Src	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:9046418-9046468	Jurkat	blood:	n/a
2	chr8:9046478-9046528	GM12891	blood:	n/a
3	chr8:9046478-9046528	LNCaP	prostate:	n/a
4	chr8:9046418-9046468	Jurkat	blood:	n/a
5	chr8:9046478-9046528	GM12891	blood:	n/a
6	chr8:9046478-9046528	LNCaP	prostate:	n/a
7	chr8:9046480-9046530	HepG2	liver:	n/a
8	chr8:9048528-9048578	GM19239	blood:	n/a
9	chr8:9048528-9048578	AG04449	skin:	fetal
10	chr8:9048528-9048578	NB4	blood:	n/a
11	chr8:9048528-9048578	HIPEpiC	eye:	n/a
12	chr8:9048528-9048578	HEK293	kidney:	embryo
13	chr8:9046478-9046528	SK-N-MC	brain:	n/a
14	chr8:9048528-9048578	HCPEpiC	choroid plexus:	n/a
15	chr8:9048528-9048578	MCF-7	breast:	n/a
16	chr8:9048528-9048578	HepG2	liver:	n/a
17	chr8:9046478-9046528	Jurkat	blood:	n/a
18	chr8:9046478-9046528	HRCEpiC	kidney:	n/a
19	chr8:9046478-9046528	NT2-D1	testis:	n/a
20	chr8:9046478-9046528	HAEpiC	amniotic membrane:	n/a
21	chr8:9055850-9055900	Jurkat	blood:	n/a
22	chr8:9046480-9046530	AG04449	skin:	fetal
23	chr8:9046480-9046530	HUVEC	blood vessel:	n/a
24	chr8:9046480-9046530	HPAEpiC	pulmonary alveolar:	n/a
25	chr8:9046418-9046468	Hepatocyte	liver:	n/a
26	chr8:9055850-9055900	HAEpiC	amniotic membrane:	n/a
27	chr8:9046480-9046530	CMK	blood:	n/a
28	chr8:9046480-9046530	HRPEpiC	eye:	n/a
29	chr8:9046480-9046530	Hela-S3	cervix:	n/a
30	chr8:9046418-9046468	NT2-D1	testis:	n/a
31	chr8:9046480-9046530	PrEC	prostate:	n/a
32	chr8:9046418-9046468	HCM	heart:	n/a
33	chr8:9055850-9055900	BE2_C	brain:	n/a
34	chr8:9055850-9055900	MCF10A-Er-Src	breast:	n/a
35	chr8:9048528-9048578	HRPEpiC	eye:	n/a
36	chr8:9048528-9048578	GM12891	blood:	n/a
37	chr8:9055850-9055900	HUVEC	blood vessel:	n/a
38	chr8:9055850-9055900	RPTEC	kidney:	n/a
39	chr8:9048528-9048578	NHBE	bronchial:	n/a
40	chr8:9048528-9048578	HCT-116	colon:	n/a
41	chr8:9046418-9046468	GM12878	blood:	n/a
42	chr8:9046480-9046530	HMEC	breast:	n/a
43	chr8:9046480-9046530	SAEC	small airway:	n/a
44	chr8:9048528-9048578	AG10803	skin:	n/a
45	chr8:9046480-9046530	T-47D	breast:	n/a
46	chr8:9046418-9046468	NHBE	bronchial:	n/a
47	chr8:9046480-9046530	SKMC	muscle:	n/a
48	chr8:9055850-9055900	HCF	heart:	n/a
49	chr8:9046478-9046528	HMEC	breast:	n/a
50	chr8:9046478-9046528	A549	lung:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:9048939..9051745-chr8:9268709..9271649,2	K562	blood:
2	chr8:9048360..9049861-chr8:9051500..9053163,2	K562	blood:
3	chr8:9055363..9058285-chr8:9064246..9065769,2	K562	blood:
4	chr8:9061535..9063157-chr8:9069276..9071088,2	MCF-7	breast:
5	chr8:9056772..9059082-chr8:9087003..9089013,2	K562	blood:
6	chr8:9048360..9049861-chr8:9051500..9053163,2	K562	blood:
7	chr8:9048360..9049931-chr8:9051500..9053085,2	K562	blood:
8	chr8:9048360..9049931-chr8:9051500..9053085,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-10A14.4.1-2	chr8:9060009-9060347	ENSG00000248538
2	lnc-RP11-10A14.4.1-2	chr8:9056378-9056501	NONHSAT124930
3	lnc-RP11-10A14.4.1-2	chr8:9060009-9060364	ENSG00000248538
4	lnc-RP11-10A14.4.1-2	chr8:9056434-9056501	ENSG00000248538
5	lnc-RP11-10A14.4.1-2	chr8:9046698-9046837	l_3542_chr8:9046697-9051717_testes
6	lnc-RP11-10A14.4.1-2	chr8:9060009-9060357	NONHSAT124930
7	lnc-RP11-10A14.4.1-2	chr8:9056434-9056501	NONHSAT124925
8	lnc-RP11-10A14.4.1-2	chr8:9046856-9047096	ENSG00000248538
9	lnc-RP11-10A14.4.1-2	chr8:9046860-9047096	NONHSAT124925
10	lnc-RP11-10A14.4.1-2	chr8:9047015-9047096	ENSG00000248538
11	lnc-RP11-10A14.4.1-2	chr8:9056434-9056501	XLOC_006705
12	lnc-RP11-10A14.4.1-2	chr8:9056434-9056501	XLOC_006705
13	lnc-RP11-10A14.4.1-2	chr8:9060009-9060363	XLOC_006705
14	lnc-RP11-10A14.4.1-2	chr8:9051468-9051542	ENSG00000248538
15	lnc-RP11-10A14.4.1-2	chr8:9046509-9046556	NONHSAT124925
16	lnc-RP11-10A14.4.1-2	chr8:9059902-9060357	NONHSAT124931
17	lnc-RP11-10A14.4.1-2	chr8:9051691-9051717	l_3542_chr8:9046697-9051717_testes
18	lnc-RP11-10A14.4.1-2	chr8:9051072-9051274	l_3542_chr8:9046697-9051717_testes
19	lnc-RP11-10A14.4.1-2	chr8:9056434-9056501	ENSG00000248538
20	lnc-RP11-10A14.4.1-2	chr8:9056378-9056501	NONHSAT124931
21	lnc-RP11-10A14.4.1-2	chr8:9046521-9046556	ENSG00000248538
22	lnc-RP11-10A14.4.1-2	chr8:9046858-9047107	XLOC_006705
23	lnc-RP11-10A14.4.1-2	chr8:9046512-9046556	XLOC_006705
24	lnc-RP11-10A14.4.1-2	chr8:9049886-9050069	l_3542_chr8:9046697-9051717_testes
25	lnc-RP11-10A14.4.1-2	chr8:9046858-9047096	XLOC_006705
26	lnc-RP11-10A14.4.1-2	chr8:9046858-9047096	ENSG00000248538
27	lnc-RP11-10A14.4.1-2	chr8:9046509-9046556	XLOC_006705
28	lnc-RP11-10A14.4.1-2	chr8:9059902-9060000	ENSG00000248538
29	lnc-RP11-10A14.4.1-2	chr8:9060009-9060366	XLOC_006705
30	lnc-RP11-10A14.4.1-2	chr8:9060009-9060368	NONHSAT124925
31	lnc-RP11-10A14.4.1-2	chr8:9056434-9056501	ENSG00000248538

Variant related genes	Relation type
ENSG00000248538	TF binding region
ENSG00000248538	CpG island

Extended variants
information (count: 923 )
Associated
traits (count: 135 )

Variant overlapped rSNPs/rCNVs (count:923 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562489431	chr8:9046233-9046234	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs181104066	chr8:9046249-9046250	Flanking Active TSS Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs528249135	chr8:9046269-9046270	Flanking Active TSS Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs530430616	chr8:9046292-9046293	Flanking Active TSS Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs147652712	chr8:9046308-9046309	Flanking Active TSS Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs1968853	chr8:9046312-9046313	Flanking Active TSS Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	mRNA abundance
7	rs140883156	chr8:9046368-9046369	Flanking Active TSS Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs186655912	chr8:9046377-9046378	Flanking Active TSS Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs189036405	chr8:9046386-9046387	Flanking Active TSS Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs538801575	chr8:9046393-9046394	Flanking Active TSS Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs551499731	chr8:9046394-9046395	Flanking Active TSS Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs150148443	chr8:9046403-9046404	Flanking Active TSS Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs117210305	chr8:9046405-9046406	Flanking Active TSS Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs537060195	chr8:9046409-9046410	Flanking Active TSS Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs115862139	chr8:9046440-9046441	Flanking Active TSS Weak transcription Enhancers Active TSS	CpG island	1 gene(s)	Overlapped CNVs	n/a
16	rs138581325	chr8:9046471-9046472	Flanking Active TSS Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs116334494	chr8:9046474-9046475	Flanking Active TSS Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs148868733	chr8:9046488-9046489	Flanking Active TSS Weak transcription Enhancers Active TSS	CpG island	1 gene(s)	Overlapped CNVs	n/a
19	rs566846055	chr8:9046498-9046499	Flanking Active TSS Weak transcription Enhancers Active TSS	CpG island	1 gene(s)	Overlapped CNVs	n/a
20	rs375432619	chr8:9046561-9046562	Flanking Active TSS Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs527444514	chr8:9046576-9046577	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs549345863	chr8:9046591-9046592	Flanking Active TSS Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs142127519	chr8:9046592-9046593	Flanking Active TSS Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs577866627	chr8:9046594-9046595	Flanking Active TSS Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs180832359	chr8:9046595-9046596	Flanking Active TSS Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs145348461	chr8:9046598-9046599	Flanking Active TSS Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs185433382	chr8:9046611-9046612	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs191034859	chr8:9046623-9046624	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs137913710	chr8:9046629-9046630	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs35720114	chr8:9046657-9046658	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs80078571	chr8:9046685-9046686	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs529851031	chr8:9046695-9046696	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs546732334	chr8:9046702-9046703	Enhancers Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
34	rs560259883	chr8:9046709-9046710	Enhancers Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
35	rs182060148	chr8:9046717-9046718	Enhancers Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
36	rs371125424	chr8:9046745-9046746	Enhancers Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
37	rs552307703	chr8:9046761-9046762	Enhancers Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
38	rs569095426	chr8:9046766-9046767	Enhancers Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
39	rs538136739	chr8:9046768-9046769	Enhancers Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
40	rs545289535	chr8:9046769-9046770	Enhancers Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
41	rs567304027	chr8:9046770-9046771	Enhancers Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
42	rs7461757	chr8:9046778-9046779	Enhancers Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
43	rs553055708	chr8:9046790-9046791	Enhancers Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
44	rs572963560	chr8:9046804-9046805	Enhancers Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
45	rs536522434	chr8:9046812-9046813	Enhancers Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
46	rs538905317	chr8:9046816-9046817	Enhancers Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
47	rs370145918	chr8:9046825-9046826	Enhancers Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
48	rs559104501	chr8:9046837-9046838	Enhancers Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
49	rs530213315	chr8:9046844-9046845	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs185943796	chr8:9046865-9046866	Enhancers Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:135)

Disease	PMID	Source
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	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
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	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
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Bladder cancer	21909424	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Developmental disorder	20461109	CNVD
abnormal development	18461090	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD

Chromatin state (count:132 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:9041200-9048200	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr8:9041400-9047800	Weak transcription	Brain Anterior Caudate	brain
3	chr8:9043200-9048000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr8:9043200-9048800	Weak transcription	Esophagus	oesophagus
5	chr8:9044600-9046400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr8:9045000-9046400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr8:9045000-9046400	Enhancers	HMEC	breast
8	chr8:9045000-9046600	Enhancers	NHEK	skin
9	chr8:9045000-9046800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr8:9045000-9047000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr8:9045000-9047200	Weak transcription	Cortex derived primary cultured neurospheres	brain
12	chr8:9045400-9046600	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
13	chr8:9045400-9048400	Enhancers	Monocytes-CD14+_RO01746	blood
14	chr8:9045400-9048600	Enhancers	Primary monocytes fromperipheralblood	blood
15	chr8:9045600-9048600	Weak transcription	NH-A	brain
16	chr8:9045800-9047200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr8:9045800-9047400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr8:9045800-9047600	Weak transcription	HUES6 Cell Line	embryonic stem cell
19	chr8:9046000-9046400	Enhancers	A549	lung
20	chr8:9046000-9047200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr8:9046000-9047200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
22	chr8:9046000-9047600	Weak transcription	HUES64 Cell Line	embryonic stem cell
23	chr8:9046000-9047600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
24	chr8:9046000-9047800	Weak transcription	HUES48 Cell Line	embryonic stem cell
25	chr8:9046200-9046400	Weak transcription	K562	blood
26	chr8:9046200-9046600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
27	chr8:9046200-9047200	Active TSS	Placenta	Placenta
28	chr8:9046200-9047600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr8:9046200-9047800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
30	chr8:9046200-9048200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr8:9046200-9048800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr8:9046400-9047400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr8:9046400-9047400	Weak transcription	A549	lung
34	chr8:9046400-9047600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr8:9046400-9047600	Weak transcription	HMEC	breast
36	chr8:9046400-9047600	Active TSS	K562	blood
37	chr8:9046600-9047000	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr8:9046800-9047200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr8:9047000-9047800	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
40	chr8:9047000-9048000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr8:9047200-9047400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr8:9047200-9047800	Flanking Active TSS	Placenta	Placenta
43	chr8:9047200-9049200	Enhancers	Primary hematopoietic stem cells short term culture	blood
44	chr8:9047200-9049400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr8:9047200-9049400	Enhancers	Cortex derived primary cultured neurospheres	brain
46	chr8:9047200-9049800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr8:9047400-9048800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr8:9047400-9049400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr8:9047400-9049400	Enhancers	iPS-20b Cell Line	embryonic stem cell
50	chr8:9047600-9047800	Enhancers	A549	lung

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