Variant report

Variant	nsv891296
Chromosome Location	chr8:111952230-112191432
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:945)
CpG islands
(count:244)
Chromatin interactive
region (count:87)
LncRNA
region (count:37)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:945 , 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	chr8:112005161-112005584	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:112055951-112056163	K562	blood:	n/a	n/a
3	ATF1	chr8:112052514-112052777	K562	blood:	n/a	n/a
4	ATF1	chr8:112055891-112056208	K562	blood:	n/a	n/a
5	ATF1	chr8:112132480-112132510	K562	blood:	n/a	n/a
6	ATF2	chr8:112162917-112163564	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr8:112162891-112163440	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr8:112001168-112001459	K562	blood:	n/a	n/a
9	BACH1	chr8:112001137-112001412	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr8:112113181-112113447	GM12878	blood:	n/a	n/a
11	BCL11A	chr8:112162971-112163355	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCL11A	chr8:112162999-112163239	H1-hESC	embryonic stem cell:	n/a	n/a
13	BCL3	chr8:112032257-112032818	K562	blood:	n/a	n/a
14	BCLAF1	chr8:112045287-112045677	K562	blood:	n/a	n/a
15	BCLAF1	chr8:112050664-112051080	K562	blood:	n/a	n/a
16	BCLAF1	chr8:112051891-112052761	K562	blood:	n/a	n/a
17	BCLAF1	chr8:112049253-112049676	K562	blood:	n/a	n/a
18	BCLAF1	chr8:112047895-112049222	K562	blood:	n/a	n/a
19	BCLAF1	chr8:112051085-112051725	K562	blood:	n/a	n/a
20	BHLHE40	chr8:112113324-112113447	K562	blood:	n/a	n/a
21	BRCA1	chr8:112152605-112152831	H1-hESC	embryonic stem cell:	n/a	n/a
22	CBX3	chr8:112052302-112052706	K562	blood:	n/a	n/a
23	CBX3	chr8:112112808-112113129	K562	blood:	n/a	n/a
24	CCNT2	chr8:112098454-112098654	K562	blood:	n/a	n/a
25	CCNT2	chr8:112053174-112053372	K562	blood:	n/a	n/a
26	CCNT2	chr8:112035228-112035538	K562	blood:	n/a	n/a
27	CEBPB	chr8:111982078-111982135	HepG2	liver:	n/a	chr8:111982113-111982124
28	CEBPB	chr8:112005374-112005612	A549	lung:	n/a	chr8:112005438-112005449
29	CEBPB	chr8:112004396-112004736	HepG2	liver:	n/a	chr8:112004519-112004532
30	CEBPB	chr8:112005317-112005565	HepG2	liver:	n/a	chr8:112005438-112005449
31	CEBPB	chr8:112005386-112005596	IMR90	lung:	n/a	chr8:112005438-112005449
32	CEBPB	chr8:112020080-112020285	A549	lung:	n/a	chr8:112020166-112020179 chr8:112020253-112020264 chr8:112020167-112020178 chr8:112020251-112020264 chr8:112020253-112020264
33	CEBPB	chr8:112152567-112153096	MCF-7	breast:	n/a	n/a
34	CEBPB	chr8:112003416-112003715	K562	blood:	n/a	chr8:112003559-112003570 chr8:112003465-112003477
35	CEBPB	chr8:112005299-112005671	HepG2	liver:	n/a	chr8:112005438-112005449
36	CEBPB	chr8:112005302-112005679	K562	blood:	n/a	chr8:112005438-112005449
37	CEBPB	chr8:112149466-112149680	HepG2	liver:	n/a	chr8:112149616-112149627
38	CEBPB	chr8:112003385-112003736	IMR90	lung:	n/a	chr8:112003559-112003570 chr8:112003465-112003477
39	CEBPB	chr8:112005347-112005579	HepG2	liver:	n/a	chr8:112005438-112005449
40	CEBPB	chr8:112101875-112101968	K562	blood:	n/a	chr8:112101947-112101958
41	CEBPB	chr8:112101790-112102112	HepG2	liver:	n/a	chr8:112101947-112101958
42	CEBPB	chr8:112181017-112181272	HepG2	liver:	n/a	chr8:112181166-112181177
43	CEBPB	chr8:112005319-112005618	K562	blood:	n/a	chr8:112005438-112005449
44	CEBPB	chr8:111988767-111988817	K562	blood:	n/a	n/a
45	CEBPB	chr8:112072418-112072646	HepG2	liver:	n/a	chr8:112072555-112072566 chr8:112072538-112072549
46	CEBPB	chr8:112057976-112058248	IMR90	lung:	n/a	n/a
47	CEBPB	chr8:112101778-112102105	H1-hESC	embryonic stem cell:	n/a	chr8:112101947-112101958
48	CEBPB	chr8:112054727-112055059	HepG2	liver:	n/a	n/a
49	CEBPB	chr8:112054708-112055042	IMR90	lung:	n/a	n/a
50	CEBPB	chr8:112004454-112004672	HepG2	liver:	n/a	chr8:112004519-112004532

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:112052376-112052426	HAEpiC	amniotic membrane:	n/a
2	chr8:112052376-112052426	HepG2	liver:	n/a
3	chr8:112053139-112053189	CMK	blood:	n/a
4	chr8:112053356-112053406	NT2-D1	testis:	n/a
5	chr8:112053139-112053189	ProgFib	skin:	n/a
6	chr8:112053356-112053406	T-47D	breast:	n/a
7	chr8:112053356-112053406	HPAEpiC	pulmonary alveolar:	n/a
8	chr8:112053139-112053189	IMR90	lung:	fetal
9	chr8:112163550-112163600	AoSMC	blood vessel:	n/a
10	chr8:112053139-112053189	HIPEpiC	eye:	n/a
11	chr8:112163550-112163600	Caco-2	colon:	n/a
12	chr8:112163550-112163600	GM12878	blood:	n/a
13	chr8:112052376-112052426	PrEC	prostate:	n/a
14	chr8:112053139-112053189	HCPEpiC	choroid plexus:	n/a
15	chr8:112053356-112053406	PANC-1	pancreas:	n/a
16	chr8:112052376-112052426	SK-N-SH	brain:	n/a
17	chr8:112053139-112053189	Caco-2	colon:	n/a
18	chr8:112163550-112163600	RPTEC	kidney:	n/a
19	chr8:112163550-112163600	GM06990	blood:	n/a
20	chr8:112053139-112053189	SKMC	muscle:	n/a
21	chr8:112163550-112163600	ovcar-3	ovarian:	n/a
22	chr8:112053139-112053189	HCT-116	colon:	n/a
23	chr8:112053356-112053406	SAEC	small airway:	n/a
24	chr8:112163550-112163600	Hepatocyte	liver:	n/a
25	chr8:112053356-112053406	Jurkat	blood:	n/a
26	chr8:112053139-112053189	NHDF-neo	bronchial:	n/a
27	chr8:112052376-112052426	ovcar-3	ovarian:	n/a
28	chr8:112052376-112052426	PANC-1	pancreas:	n/a
29	chr8:112053139-112053189	SAEC	small airway:	n/a
30	chr8:112053139-112053189	AG04450	lung:	fetal
31	chr8:112163550-112163600	HUVEC	blood vessel:	n/a
32	chr8:112163550-112163600	NT2-D1	testis:	n/a
33	chr8:112053356-112053406	AG09309	skin:	n/a
34	chr8:112052376-112052426	HCT-116	colon:	n/a
35	chr8:112053139-112053189	PFSK-1	brain:	n/a
36	chr8:112053139-112053189	HUVEC	blood vessel:	n/a
37	chr8:112163550-112163600	NH-A	brain:	n/a
38	chr8:112053139-112053189	SK-N-SH	brain:	n/a
39	chr8:112052376-112052426	HRPEpiC	eye:	n/a
40	chr8:112163550-112163600	SAEC	small airway:	n/a
41	chr8:112053139-112053189	HepG2	liver:	n/a
42	chr8:112053356-112053406	LNCaP	prostate:	n/a
43	chr8:112053356-112053406	ovcar-3	ovarian:	n/a
44	chr8:112053139-112053189	AG09319	gingival:	n/a
45	chr8:112053356-112053406	BJ	skin:	n/a
46	chr8:112052376-112052426	ECC-1	luminal epithelium:	n/a
47	chr8:112053356-112053406	U87	brain:	n/a
48	chr8:112053356-112053406	NB4	blood:	n/a
49	chr8:112053356-112053406	AG09319	gingival:	n/a
50	chr8:112163550-112163600	HAEpiC	amniotic membrane:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr8:112054463..112057447-chr8:112061238..112063289,2	K562	blood:
2	chr8:112047893..112049980-chr8:112071535..112074858,3	K562	blood:
3	chr8:112142087..112143993-chr8:112151164..112153566,2	MCF-7	breast:
4	chr8:112048936..112050603-chr8:112056318..112058671,2	K562	blood:
5	chr8:112023343..112027872-chr8:112028215..112031579,4	K562	blood:
6	chr8:112152211..112153851-chr8:112248272..112249455,10	MCF-7	breast:
7	chr8:112142087..112143993-chr8:112151164..112153566,2	MCF-7	breast:
8	chr8:112049821..112051426-chr8:112052995..112056257,3	K562	blood:
9	chr8:111877803..111878676-chr8:112126153..112126932,3	MCF-7	breast:
10	chr8:111986722..111988349-chr8:112001568..112003641,2	K562	blood:
11	chr8:112073611..112075207-chr8:112079150..112081817,2	MCF-7	breast:
12	chr8:112046473..112049277-chr8:112050883..112054393,4	K562	blood:
13	chr8:112115345..112116966-chr8:112124670..112126786,2	MCF-7	breast:
14	chr8:112152279..112153092-chr8:121617588..121618297,2	MCF-7	breast:
15	chr8:112024408..112026830-chr8:112028447..112030493,2	K562	blood:
16	chr8:112133641..112134299-chr9:13359583..13360482,2	MCF-7	breast:
17	chr8:112154689..112157253-chr8:112157958..112160941,2	MCF-7	breast:
18	chr8:112127583..112130124-chr8:112133579..112135146,2	MCF-7	breast:
19	chr8:111952441..111954881-chr8:111958633..111961171,2	K562	blood:
20	chr8:112166075..112166697-chr8:112248498..112249074,2	MCF-7	breast:
21	chr8:111993072..111993615-chr8:112265097..112265675,2	MCF-7	breast:
22	chr8:112044268..112046186-chr8:112050654..112052583,2	K562	blood:
23	chr8:112023343..112027872-chr8:112028215..112031579,4	K562	blood:
24	chr8:112127583..112130124-chr8:112133579..112135146,2	MCF-7	breast:
25	chr8:112092554..112095223-chr8:112096856..112098486,2	MCF-7	breast:
26	chr8:112046473..112049277-chr8:112050883..112054393,4	K562	blood:
27	chr8:112115345..112116966-chr8:112124670..112126786,2	MCF-7	breast:
28	chr8:112092554..112095223-chr8:112096856..112098486,2	MCF-7	breast:
29	chr8:112001101..112002648-chr8:112002795..112004747,2	K562	blood:
30	chr8:112040792..112044019-chr8:112049363..112052232,3	K562	blood:
31	chr8:112020517..112022084-chr8:112022778..112025177,2	K562	blood:
32	chr8:112037306..112039469-chr8:112041170..112043078,2	K562	blood:
33	chr8:111977359..111979519-chr8:111986099..111987901,2	K562	blood:
34	chr8:111924377..111926908-chr8:111953183..111955700,2	K562	blood:
35	chr8:112048936..112050603-chr8:112056318..112058671,2	K562	blood:
36	chr8:112054463..112057447-chr8:112061238..112063289,2	K562	blood:
37	chr8:112045873..112047633-chr8:112047967..112049827,3	K562	blood:
38	chr5:173612522..173613033-chr8:112023628..112024312,2	MCF-7	breast:
39	chr8:112050824..112052774-chr8:112058514..112060198,2	K562	blood:
40	chr8:112152351..112153276-chr8:112265083..112266006,7	MCF-7	breast:
41	chr8:112051929..112053704-chr8:112063619..112066974,3	K562	blood:
42	chr8:112121761..112124184-chr8:112126207..112129085,2	K562	blood:
43	chr8:111986722..111988349-chr8:112001568..112003641,2	K562	blood:
44	chr8:112164287..112166378-chr8:112180703..112183075,2	MCF-7	breast:
45	chr8:112040792..112044019-chr8:112049363..112052232,3	K562	blood:
46	chr8:112154689..112157253-chr8:112157958..112160941,2	MCF-7	breast:
47	chr8:112052147..112053672-chr8:112062800..112065119,2	K562	blood:
48	chr8:112152279..112153172-chr8:112264812..112266234,7	MCF-7	breast:
49	chr1:120421655..120422591-chr8:112129482..112130279,2	MCF-7	breast:
50	chr8:111948692..111950464-chr8:111998456..112000368,2	MCF-7	breast:

(count:37 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KCNV1-7	chr8:112086929-112087054	l_3667_chr8:112084787-112108928_brain
2	lnc-RP11-422N16.3.1-6	chr8:112000263-112000924	FPKM1_group_31989_transcript_3
3	lnc-KCNV1-2	chr8:111995179-111995369	ENSG00000253877
4	lnc-KCNV1-2	chr8:112017759-112017878	XLOC_007182
5	lnc-KCNV1-7	chr8:112096343-112096437	l_3667_chr8:112084787-112108928_brain
6	lnc-KCNV1-7	chr8:112084788-112084855	l_3667_chr8:112084787-112108928_brain
7	lnc-KCNV1-2	chr8:112015643-112015679	ENSG00000253877
8	lnc-KCNV1-2	chr8:111993626-111995369	XLOC_007182
9	lnc-KCNV1-2	chr8:112015643-112015679	XLOC_007182
10	lnc-KCNV1-2	chr8:112039535-112039752	XLOC_007182
11	lnc-KCNV1-2	chr8:112016890-112016998	XLOC_007182
12	lnc-KCNV1-2	chr8:112039535-112039621	ENSG00000253877
13	lnc-KCNV1-2	chr8:112039535-112039641	XLOC_007182
14	lnc-KCNV1-7	chr8:112108711-112108928	l_3667_chr8:112084787-112108928_brain
15	lnc-KCNV1-2	chr8:112039535-112039662	ENSG00000253877
16	lnc-KCNV1-2	chr8:112039535-112039752	XLOC_007182
17	lnc-CSMD3-3	chr8:112111190-112111368	ENSG00000253103
18	lnc-RP11-422N16.3.1-6	chr8:112000263-112000924	NONHSAT128319
19	lnc-KCNV1-2	chr8:112017759-112017878	XLOC_007182
20	lnc-KCNV1-2	chr8:112016890-112016917	XLOC_007182
21	lnc-KCNV1-2	chr8:111991098-111995369	XLOC_007182
22	lnc-RP11-422N16.3.1-7	chr8:112174769-112174905	l_3668_chr8:112174768-112194925_testes
23	lnc-CSMD3-3	chr8:112125661-112125749	ENSG00000253103
24	lnc-KCNV1-2	chr8:111994744-111995369	XLOC_007182
25	lnc-KCNV1-2	chr8:112017759-112017878	ENSG00000253877
26	lnc-KCNV1-2	chr8:112015643-112015679	XLOC_007182
27	lnc-KCNV1-2	chr8:112015643-112015679	XLOC_007182
28	lnc-KCNV1-2	chr8:112016890-112016998	ENSG00000253877
29	lnc-KCNV1-2	chr8:112017759-112017878	ENSG00000253877
30	lnc-CSMD3-3	chr8:112128764-112128829	ENSG00000253103
31	lnc-RP11-422N16.3.1-6	chr8:112000448-112001045	FPKM1_group_31989_transcript_3
32	lnc-KCNV1-7	chr8:112086066-112086174	l_3667_chr8:112084787-112108928_brain
33	lnc-RP11-422N16.3.1-6	chr8:112002113-112002710	NONHSAT128319
34	lnc-KCNV1-2	chr8:112015643-112015679	ENSG00000253877
35	lnc-KCNV1-2	chr8:112016890-112016998	ENSG00000253877
36	lnc-KCNV1-2	chr8:112027133-112027261	ENSG00000253877
37	lnc-CSMD3-2	chr8:112191422-112191587	ENSG00000253489

No data

Variant related genes	Relation type
ENSG00000253877	TF binding region
ENSG00000253877	CpG island
ENSG00000253877	chromatin interactions
ENSG00000253103	chromatin interactions
DNMT1	miRNA target sites
ZEB2	miRNA target sites
ZFPM2	miRNA target sites
CDC42	miRNA target sites
TFRC	miRNA target sites
AADACL3	miRNA target sites

Extended variants
information (count: 4462 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:4462 , 50 per page) page: 1 2 3 4 5 6 7 ... 90

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4289849	chr8:111952230-111952231	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs116577384	chr8:111952277-111952278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs557839596	chr8:111952312-111952313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs577724647	chr8:111952353-111952354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs113539684	chr8:111952400-111952401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs571357082	chr8:111952410-111952411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs573966928	chr8:111952417-111952418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs542982638	chr8:111952442-111952443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs376911221	chr8:111952458-111952459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs113318713	chr8:111952519-111952520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs541123848	chr8:111952525-111952526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs564617638	chr8:111952528-111952529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs533332857	chr8:111952631-111952632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs549943697	chr8:111952633-111952634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs527283344	chr8:111952636-111952637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs185241282	chr8:111952661-111952662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs142714847	chr8:111952688-111952689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs549314458	chr8:111952704-111952705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs35158889	chr8:111952709-111952710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs112914942	chr8:111952710-111952711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs534622413	chr8:111952719-111952720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs557533812	chr8:111952728-111952729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs181766860	chr8:111952780-111952781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs371933624	chr8:111952793-111952794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs571341135	chr8:111952853-111952854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs536779928	chr8:111952914-111952915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs557183632	chr8:111952979-111952980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs370877010	chr8:111952986-111952987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs77755065	chr8:111953613-111953614	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs113148862	chr8:111953626-111953627	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs573863183	chr8:111953632-111953633	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs369665887	chr8:111953649-111953650	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs191417397	chr8:111953653-111953654	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs528772821	chr8:111953712-111953713	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs551834260	chr8:111953721-111953722	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs564850655	chr8:111953758-111953759	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs376126444	chr8:111953827-111953828	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs530528772	chr8:111953831-111953832	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs550658824	chr8:111953842-111953843	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs567389644	chr8:111953900-111953901	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs536378620	chr8:111953914-111953915	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs79220047	chr8:111953973-111953974	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs566592343	chr8:111953990-111953991	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs113849441	chr8:111954005-111954006	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs200752583	chr8:111954054-111954055	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs558580221	chr8:111954076-111954077	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs183609109	chr8:111954093-111954094	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs76904610	chr8:111954094-111954095	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs536882675	chr8:111954159-111954160	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs557009234	chr8:111954183-111954184	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
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
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	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
abnormal development	18461090	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
Cancer	16751803	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
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Chronic myeloid leukemia	21384125	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Neuroticism	17667963	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	21163964	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:216 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:111951000-111953000	Weak transcription	Brain Hippocampus Middle	brain
2	chr8:111953600-111954200	Enhancers	Fetal Heart	heart
3	chr8:111958200-111958600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr8:111958600-111959800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr8:111959800-111960600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr8:111969200-111979600	Weak transcription	K562	blood
7	chr8:111970200-111970400	Enhancers	Brain Angular Gyrus	brain
8	chr8:111971000-111971200	Enhancers	Brain Angular Gyrus	brain
9	chr8:111971800-111972600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr8:111977800-111978200	Enhancers	Brain Substantia Nigra	brain
11	chr8:111978000-111978400	Enhancers	Fetal Brain Male	brain
12	chr8:111978200-111989400	Weak transcription	Brain Substantia Nigra	brain
13	chr8:111984200-111984800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr8:111989200-111989800	Enhancers	Brain Cingulate Gyrus	brain
15	chr8:111989400-111989600	Enhancers	Brain Hippocampus Middle	brain
16	chr8:111989400-111990000	Enhancers	Brain Substantia Nigra	brain
17	chr8:111989800-111993400	Weak transcription	Brain Hippocampus Middle	brain
18	chr8:111989800-111995000	Weak transcription	Brain Cingulate Gyrus	brain
19	chr8:111990000-111995200	Weak transcription	Brain Substantia Nigra	brain
20	chr8:111990400-111990600	Enhancers	Brain Inferior Temporal Lobe	brain
21	chr8:111990800-111993400	Weak transcription	Brain Inferior Temporal Lobe	brain
22	chr8:111993400-111993600	Enhancers	Brain Hippocampus Middle	brain
23	chr8:111993400-111993600	Enhancers	Brain Inferior Temporal Lobe	brain
24	chr8:111993600-111994000	Enhancers	Fetal Brain Male	brain
25	chr8:111993600-111995000	Weak transcription	Brain Hippocampus Middle	brain
26	chr8:111993600-111995200	Weak transcription	Brain Inferior Temporal Lobe	brain
27	chr8:111995000-111995200	Flanking Active TSS	Brain Hippocampus Middle	brain
28	chr8:111995000-111995600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr8:111995000-111995600	Active TSS	Brain Cingulate Gyrus	brain
30	chr8:111995200-111995600	Active TSS	Brain Hippocampus Middle	brain
31	chr8:111995200-111995800	Enhancers	Brain Angular Gyrus	brain
32	chr8:111995200-111995800	Active TSS	Brain Inferior Temporal Lobe	brain
33	chr8:111995200-111995800	Enhancers	Brain Substantia Nigra	brain
34	chr8:111995600-111995800	Flanking Active TSS	Brain Hippocampus Middle	brain
35	chr8:111995600-112009200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr8:112003400-112004600	Enhancers	HepG2	liver
37	chr8:112004600-112005000	Enhancers	Brain Substantia Nigra	brain
38	chr8:112004600-112005400	Flanking Active TSS	HepG2	liver
39	chr8:112004800-112005000	Enhancers	Brain Hippocampus Middle	brain
40	chr8:112005000-112006800	Weak transcription	Brain Hippocampus Middle	brain
41	chr8:112006800-112008600	Enhancers	Brain Hippocampus Middle	brain
42	chr8:112007000-112007800	Enhancers	Brain Inferior Temporal Lobe	brain
43	chr8:112007200-112007400	Enhancers	Brain Cingulate Gyrus	brain
44	chr8:112007400-112008400	Weak transcription	Brain Cingulate Gyrus	brain
45	chr8:112007800-112008400	Weak transcription	Brain Inferior Temporal Lobe	brain
46	chr8:112008200-112008400	Enhancers	Brain Angular Gyrus	brain
47	chr8:112008200-112008800	Enhancers	Brain Anterior Caudate	brain
48	chr8:112008400-112008600	Enhancers	Brain Cingulate Gyrus	brain
49	chr8:112008400-112008600	Enhancers	Brain Inferior Temporal Lobe	brain
50	chr8:112008400-112009800	Weak transcription	Brain Angular Gyrus	brain

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