Variant report

Variant	nsv1028079
Chromosome Location	chr8:111939568-112098196
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:487)
CpG islands
(count:183)
Chromatin interactive
region (count:55)
LncRNA
region (count:32)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:487 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:112055951-112056163	K562	blood:	n/a	n/a
2	ARID3A	chr8:112005161-112005584	HepG2	liver:	n/a	n/a
3	ATF1	chr8:112055891-112056208	K562	blood:	n/a	n/a
4	ATF1	chr8:112052514-112052777	K562	blood:	n/a	n/a
5	BACH1	chr8:112001137-112001412	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr8:112001168-112001459	K562	blood:	n/a	n/a
7	BCL3	chr8:112032257-112032818	K562	blood:	n/a	n/a
8	BCLAF1	chr8:112051085-112051725	K562	blood:	n/a	n/a
9	BCLAF1	chr8:112050664-112051080	K562	blood:	n/a	n/a
10	BCLAF1	chr8:112047895-112049222	K562	blood:	n/a	n/a
11	BCLAF1	chr8:112045287-112045677	K562	blood:	n/a	n/a
12	BCLAF1	chr8:112049253-112049676	K562	blood:	n/a	n/a
13	BCLAF1	chr8:112051891-112052761	K562	blood:	n/a	n/a
14	CBX3	chr8:112052302-112052706	K562	blood:	n/a	n/a
15	CCNT2	chr8:112035228-112035538	K562	blood:	n/a	n/a
16	CCNT2	chr8:112053174-112053372	K562	blood:	n/a	n/a
17	CEBPB	chr8:112057976-112058248	IMR90	lung:	n/a	n/a
18	CEBPB	chr8:112003416-112003715	K562	blood:	n/a	chr8:112003559-112003570 chr8:112003465-112003477
19	CEBPB	chr8:112003382-112003710	HepG2	liver:	n/a	chr8:112003559-112003570 chr8:112003465-112003477
20	CEBPB	chr8:112005299-112005671	HepG2	liver:	n/a	chr8:112005438-112005449
21	CEBPB	chr8:112005291-112005662	Hela-S3	cervix:	n/a	chr8:112005438-112005449
22	CEBPB	chr8:112005317-112005565	HepG2	liver:	n/a	chr8:112005438-112005449
23	CEBPB	chr8:112003396-112003657	A549	lung:	n/a	chr8:112003559-112003570 chr8:112003465-112003477
24	CEBPB	chr8:112044174-112044499	HepG2	liver:	n/a	chr8:112044333-112044344
25	CEBPB	chr8:112005205-112005680	HepG2	liver:	n/a	chr8:112005438-112005449
26	CEBPB	chr8:111988767-111988817	K562	blood:	n/a	n/a
27	CEBPB	chr8:112005386-112005596	IMR90	lung:	n/a	chr8:112005438-112005449
28	CEBPB	chr8:111950443-111950740	HepG2	liver:	n/a	chr8:111950580-111950591
29	CEBPB	chr8:112004454-112004672	HepG2	liver:	n/a	chr8:112004519-112004532
30	CEBPB	chr8:112005302-112005679	K562	blood:	n/a	chr8:112005438-112005449
31	CEBPB	chr8:112003385-112003736	IMR90	lung:	n/a	chr8:112003559-112003570 chr8:112003465-112003477
32	CEBPB	chr8:112054708-112055042	IMR90	lung:	n/a	n/a
33	CEBPB	chr8:112020022-112020325	IMR90	lung:	n/a	chr8:112020166-112020179 chr8:112020253-112020264 chr8:112020167-112020178 chr8:112020251-112020264 chr8:112020253-112020264
34	CEBPB	chr8:112054705-112055080	K562	blood:	n/a	n/a
35	CEBPB	chr8:112054718-112055073	A549	lung:	n/a	n/a
36	CEBPB	chr8:112005347-112005579	HepG2	liver:	n/a	chr8:112005438-112005449
37	CEBPB	chr8:111992078-111992115	HepG2	liver:	n/a	n/a
38	CEBPB	chr8:112072418-112072646	HepG2	liver:	n/a	chr8:112072555-112072566 chr8:112072538-112072549
39	CEBPB	chr8:112004396-112004736	HepG2	liver:	n/a	chr8:112004519-112004532
40	CEBPB	chr8:111950419-111950748	H1-hESC	embryonic stem cell:	n/a	chr8:111950580-111950591
41	CEBPB	chr8:112005329-112005586	MCF-7	breast:	n/a	chr8:112005438-112005449
42	CEBPB	chr8:111989225-111989607	MCF-7	breast:	n/a	chr8:111989417-111989430 chr8:111989417-111989428 chr8:111989417-111989430 chr8:111989417-111989428
43	CEBPB	chr8:112054880-112054909	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr8:112072478-112072685	IMR90	lung:	n/a	chr8:112072555-112072566 chr8:112072538-112072549
45	CEBPB	chr8:112003439-112003699	Hela-S3	cervix:	n/a	chr8:112003559-112003570 chr8:112003465-112003477
46	CEBPB	chr8:112044195-112044491	K562	blood:	n/a	chr8:112044333-112044344
47	CEBPB	chr8:111992769-111993050	HepG2	liver:	n/a	chr8:111992861-111992872
48	CEBPB	chr8:112020047-112020339	HepG2	liver:	n/a	chr8:112020166-112020179 chr8:112020253-112020264 chr8:112020167-112020178 chr8:112020251-112020264 chr8:112020253-112020264
49	CEBPB	chr8:112058029-112058214	K562	blood:	n/a	n/a
50	CEBPB	chr8:112005374-112005612	A549	lung:	n/a	chr8:112005438-112005449

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:112053139-112053189	HRE	kidney:	n/a
2	chr8:112052376-112052426	HAEpiC	amniotic membrane:	n/a
3	chr8:112053139-112053189	AG10803	skin:	n/a
4	chr8:112052376-112052426	ovcar-3	ovarian:	n/a
5	chr8:112052376-112052426	HRCEpiC	kidney:	n/a
6	chr8:112052376-112052426	HEK293	kidney:	embryo
7	chr8:112052376-112052426	NB4	blood:	n/a
8	chr8:112052376-112052426	T-47D	breast:	n/a
9	chr8:112053356-112053406	NT2-D1	testis:	n/a
10	chr8:112053356-112053406	HCF	heart:	n/a
11	chr8:112053139-112053189	AG04450	lung:	fetal
12	chr8:112053356-112053406	Hepatocyte	liver:	n/a
13	chr8:112053356-112053406	HCM	heart:	n/a
14	chr8:112053356-112053406	K562	blood:	n/a
15	chr8:112053139-112053189	HUVEC	blood vessel:	n/a
16	chr8:112053356-112053406	Hela-S3	cervix:	n/a
17	chr8:112053139-112053189	AG09309	skin:	n/a
18	chr8:112053356-112053406	T-47D	breast:	n/a
19	chr8:112053139-112053189	SK-N-SH	brain:	n/a
20	chr8:112053356-112053406	NH-A	brain:	n/a
21	chr8:112053356-112053406	ProgFib	skin:	n/a
22	chr8:112053139-112053189	Caco-2	colon:	n/a
23	chr8:112052376-112052426	K562	blood:	n/a
24	chr8:112052376-112052426	HCPEpiC	choroid plexus:	n/a
25	chr8:112053139-112053189	AG04449	skin:	fetal
26	chr8:112053139-112053189	HIPEpiC	eye:	n/a
27	chr8:112053139-112053189	HCT-116	colon:	n/a
28	chr8:112053139-112053189	HMEC	breast:	n/a
29	chr8:112053139-112053189	HepG2	liver:	n/a
30	chr8:112052376-112052426	IMR90	lung:	fetal
31	chr8:112053356-112053406	GM12878	blood:	n/a
32	chr8:112052376-112052426	GM12878	blood:	n/a
33	chr8:112053356-112053406	MCF-7	breast:	n/a
34	chr8:112053139-112053189	GM12891	blood:	n/a
35	chr8:112053139-112053189	SAEC	small airway:	n/a
36	chr8:112053356-112053406	HL-60	blood:	n/a
37	chr8:112053139-112053189	AG09319	gingival:	n/a
38	chr8:112053139-112053189	T-47D	breast:	n/a
39	chr8:112053356-112053406	Jurkat	blood:	n/a
40	chr8:112052376-112052426	H1-hESC	embryonic stem cell:	embryo
41	chr8:112053139-112053189	Hela-S3	cervix:	n/a
42	chr8:112053356-112053406	LNCaP	prostate:	n/a
43	chr8:112053356-112053406	HepG2	liver:	n/a
44	chr8:112053139-112053189	GM12892	blood:	n/a
45	chr8:112053356-112053406	NB4	blood:	n/a
46	chr8:112053139-112053189	SK-N-SH_RA	brain:	n/a
47	chr8:112053356-112053406	GM12892	blood:	n/a
48	chr8:112052376-112052426	AG09319	gingival:	n/a
49	chr8:112053356-112053406	HEEpiC	esophagus:	n/a
50	chr8:112053139-112053189	NHBE	bronchial:	n/a

(count:55 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:112040792..112044019-chr8:112049363..112052232,3	K562	blood:
2	chr8:112001101..112002648-chr8:112002795..112004747,2	K562	blood:
3	chr8:112073611..112075207-chr8:112079150..112081817,2	MCF-7	breast:
4	chr8:112023343..112027872-chr8:112028215..112031579,4	K562	blood:
5	chr8:112023343..112027872-chr8:112028215..112031579,4	K562	blood:
6	chr8:111948692..111950464-chr8:111998456..112000368,2	MCF-7	breast:
7	chr8:112049821..112051426-chr8:112052995..112056257,3	K562	blood:
8	chr8:111986722..111988349-chr8:112001568..112003641,2	K562	blood:
9	chr8:112069491..112071465-chr8:112075168..112076781,2	K562	blood:
10	chr8:112040792..112044019-chr8:112049363..112052232,3	K562	blood:
11	chr8:111993072..111993615-chr8:112265097..112265675,2	MCF-7	breast:
12	chr8:111877768..111878423-chr8:111945734..111946406,2	MCF-7	breast:
13	chr8:112073611..112075207-chr8:112079150..112081817,2	MCF-7	breast:
14	chr8:112045873..112047633-chr8:112047967..112049827,3	K562	blood:
15	chr8:112046473..112049277-chr8:112050883..112054393,4	K562	blood:
16	chr8:111977359..111979519-chr8:111986099..111987901,2	K562	blood:
17	chr8:112026713..112028384-chr8:112038537..112040451,2	K562	blood:
18	chr8:111924377..111926908-chr8:111953183..111955700,2	K562	blood:
19	chr8:112049821..112051426-chr8:112052995..112056257,3	K562	blood:
20	chr8:112048936..112050603-chr8:112056318..112058671,2	K562	blood:
21	chr8:112024408..112026830-chr8:112028447..112030493,2	K562	blood:
22	chr8:112049920..112051426-chr8:112052995..112055202,2	K562	blood:
23	chr8:112020517..112022084-chr8:112022778..112025177,2	K562	blood:
24	chr8:112051929..112053704-chr8:112063619..112066974,3	K562	blood:
25	chr8:111952441..111954881-chr8:111958633..111961171,2	K562	blood:
26	chr8:112092554..112095223-chr8:112096856..112098486,2	MCF-7	breast:
27	chr8:112054463..112057447-chr8:112061238..112063289,2	K562	blood:
28	chr8:112045873..112047633-chr8:112047967..112049827,3	K562	blood:
29	chr8:112037306..112039469-chr8:112041170..112043078,2	K562	blood:
30	chr5:173612522..173613033-chr8:112023628..112024312,2	MCF-7	breast:
31	chr8:111986722..111988349-chr8:112001568..112003641,2	K562	blood:
32	chr8:112037306..112039469-chr8:112041170..112043078,2	K562	blood:
33	chr8:112020517..112022084-chr8:112022778..112025177,2	K562	blood:
34	chr8:112069491..112071465-chr8:112075168..112076781,2	K562	blood:
35	chr8:112048936..112050603-chr8:112056318..112058671,2	K562	blood:
36	chr5:159495628..159496384-chr8:112067763..112068421,2	MCF-7	breast:
37	chr8:112044268..112046186-chr8:112050654..112052583,2	K562	blood:
38	chr8:112050824..112052774-chr8:112058514..112060198,2	K562	blood:
39	chr8:112001101..112002648-chr8:112002795..112004747,2	K562	blood:
40	chr8:112092554..112095223-chr8:112096856..112098486,2	MCF-7	breast:
41	chr8:112024408..112026830-chr8:112028447..112030493,2	K562	blood:
42	chr8:112044268..112046186-chr8:112050654..112052583,2	K562	blood:
43	chr8:111905363..111907255-chr8:112045592..112048412,2	K562	blood:
44	chr8:112052147..112053672-chr8:112062800..112065119,2	K562	blood:
45	chr8:111952441..111954881-chr8:111958633..111961171,2	K562	blood:
46	chr8:111977359..111979519-chr8:111986099..111987901,2	K562	blood:
47	chr8:112049920..112051426-chr8:112052995..112055202,2	K562	blood:
48	chr8:112047893..112049980-chr8:112071535..112074858,3	K562	blood:
49	chr8:112050824..112052774-chr8:112058514..112060198,2	K562	blood:
50	chr8:112051929..112053704-chr8:112063619..112066974,3	K562	blood:

(count:32 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KCNV1-2	chr8:111995179-111995369	ENSG00000253877
2	lnc-KCNV1-2	chr8:112016890-112016998	XLOC_007182
3	lnc-KCNV1-7	chr8:112086066-112086174	l_3667_chr8:112084787-112108928_brain
4	lnc-KCNV1-2	chr8:112017759-112017878	ENSG00000253877
5	lnc-KCNV1-7	chr8:112084788-112084855	l_3667_chr8:112084787-112108928_brain
6	lnc-RP11-422N16.3.1-6	chr8:112000263-112000924	FPKM1_group_31989_transcript_3
7	lnc-KCNV1-2	chr8:112015643-112015679	XLOC_007182
8	lnc-KCNV1-2	chr8:112039535-112039621	ENSG00000253877
9	lnc-KCNV1-2	chr8:111994744-111995369	XLOC_007182
10	lnc-KCNV1-2	chr8:112016890-112016998	ENSG00000253877
11	lnc-RP11-422N16.3.1-6	chr8:112002113-112002710	NONHSAT128319
12	lnc-RP11-422N16.3.1-6	chr8:112000263-112000924	NONHSAT128319
13	lnc-KCNV1-2	chr8:112017759-112017878	XLOC_007182
14	lnc-KCNV1-2	chr8:112015643-112015679	ENSG00000253877
15	lnc-KCNV1-2	chr8:112039535-112039662	ENSG00000253877
16	lnc-KCNV1-2	chr8:112016890-112016998	ENSG00000253877
17	lnc-KCNV1-2	chr8:112017759-112017878	ENSG00000253877
18	lnc-KCNV1-2	chr8:112015643-112015679	ENSG00000253877
19	lnc-KCNV1-2	chr8:112039535-112039752	XLOC_007182
20	lnc-KCNV1-2	chr8:112015643-112015679	XLOC_007182
21	lnc-RP11-422N16.3.1-6	chr8:112000448-112001045	FPKM1_group_31989_transcript_3
22	lnc-KCNV1-2	chr8:112017759-112017878	XLOC_007182
23	lnc-KCNV1-7	chr8:112086929-112087054	l_3667_chr8:112084787-112108928_brain
24	lnc-KCNV1-2	chr8:112016890-112016917	XLOC_007182
25	lnc-KCNV1-2	chr8:112039535-112039752	XLOC_007182
26	lnc-KCNV1-2	chr8:111993626-111995369	XLOC_007182
27	lnc-KCNV1-2	chr8:112039535-112039641	XLOC_007182
28	lnc-KCNV1-2	chr8:111949919-111949956	ENSG00000253877
29	lnc-KCNV1-2	chr8:111991098-111995369	XLOC_007182
30	lnc-KCNV1-2	chr8:112015643-112015679	XLOC_007182
31	lnc-KCNV1-2	chr8:112027133-112027261	ENSG00000253877
32	lnc-KCNV1-7	chr8:112096343-112096437	l_3667_chr8:112084787-112108928_brain

No data

Variant related genes	Relation type
ENSG00000253877	TF binding region
ENSG00000254241	TF binding region
ENSG00000253877	CpG island
ENSG00000254241	CpG island
ENSG00000253877	chromatin interactions
ZFPM2	miRNA target sites
TFRC	miRNA target sites
ZEB2	miRNA target sites
AADACL3	miRNA target sites
CDC42	miRNA target sites
DNMT1	miRNA target sites

Extended variants
information (count: 3731 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:3731 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs570853157	chr8:111939572-111939573	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs533413653	chr8:111939593-111939594	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs550199513	chr8:111939610-111939611	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs545851280	chr8:111939619-111939620	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs115504751	chr8:111939623-111939624	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs143228134	chr8:111939639-111939640	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs555702532	chr8:111939710-111939711	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs181477736	chr8:111939734-111939735	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs186376431	chr8:111939754-111939755	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs558070562	chr8:111939834-111939835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs79098143	chr8:111939846-111939847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs543025700	chr8:111939967-111939968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs552819011	chr8:111939981-111939982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs542738185	chr8:111939995-111939996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs191950046	chr8:111940004-111940005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs183009582	chr8:111940018-111940019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs187458932	chr8:111940049-111940050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs545321284	chr8:111940050-111940051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs368191665	chr8:111940069-111940070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs565179333	chr8:111940154-111940155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs566081904	chr8:111940168-111940169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs533322215	chr8:111940277-111940278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs549919854	chr8:111940295-111940296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs142651568	chr8:111940409-111940410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs4143847	chr8:111940430-111940431	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs34339789	chr8:111940522-111940523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs530777741	chr8:111940526-111940527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs549490865	chr8:111940527-111940528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs565923963	chr8:111940528-111940529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs534933451	chr8:111940587-111940588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs371283008	chr8:111940639-111940640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs146012972	chr8:111940668-111940669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs373912932	chr8:111940669-111940670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs114986898	chr8:111940717-111940718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs537023020	chr8:111940784-111940785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs556661608	chr8:111940821-111940822	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs138631724	chr8:111940826-111940827	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs535959570	chr8:111940830-111940831	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs553081592	chr8:111940835-111940836	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs573029399	chr8:111940876-111940877	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs564239416	chr8:111940878-111940879	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs545230985	chr8:111940886-111940887	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs565140926	chr8:111940957-111940958	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs575628755	chr8:111940960-111940961	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs544521342	chr8:111941066-111941067	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs574667234	chr8:111941143-111941144	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs150221877	chr8:111941183-111941184	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs563517015	chr8:111941226-111941227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs529328916	chr8:111941227-111941228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs549204570	chr8:111941258-111941259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

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

Chromatin state (count:169 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:111929600-111942400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr8:111939200-111939800	Enhancers	HUES6 Cell Line	embryonic stem cell
3	chr8:111939400-111939600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr8:111939800-111940800	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr8:111940800-111941200	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr8:111942400-111942600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr8:111943600-111944800	Enhancers	Muscle Satellite Cultured Cells	--
8	chr8:111943800-111944200	Enhancers	HSMM	muscle
9	chr8:111943800-111944400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr8:111950000-111951200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr8:111950000-111951200	Enhancers	Cortex derived primary cultured neurospheres	brain
12	chr8:111950200-111951200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr8:111950400-111950800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr8:111950600-111951000	Enhancers	Brain Hippocampus Middle	brain
15	chr8:111950600-111951200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
16	chr8:111950600-111951400	Enhancers	Brain Cingulate Gyrus	brain
17	chr8:111951000-111953000	Weak transcription	Brain Hippocampus Middle	brain
18	chr8:111951400-111951800	Weak transcription	Brain Cingulate Gyrus	brain
19	chr8:111951800-111952200	Enhancers	Brain Cingulate Gyrus	brain
20	chr8:111953600-111954200	Enhancers	Fetal Heart	heart
21	chr8:111958200-111958600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr8:111958600-111959800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr8:111959800-111960600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr8:111969200-111979600	Weak transcription	K562	blood
25	chr8:111970200-111970400	Enhancers	Brain Angular Gyrus	brain
26	chr8:111971000-111971200	Enhancers	Brain Angular Gyrus	brain
27	chr8:111971800-111972600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr8:111977800-111978200	Enhancers	Brain Substantia Nigra	brain
29	chr8:111978000-111978400	Enhancers	Fetal Brain Male	brain
30	chr8:111978200-111989400	Weak transcription	Brain Substantia Nigra	brain
31	chr8:111984200-111984800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr8:111989200-111989800	Enhancers	Brain Cingulate Gyrus	brain
33	chr8:111989400-111989600	Enhancers	Brain Hippocampus Middle	brain
34	chr8:111989400-111990000	Enhancers	Brain Substantia Nigra	brain
35	chr8:111989800-111993400	Weak transcription	Brain Hippocampus Middle	brain
36	chr8:111989800-111995000	Weak transcription	Brain Cingulate Gyrus	brain
37	chr8:111990000-111995200	Weak transcription	Brain Substantia Nigra	brain
38	chr8:111990400-111990600	Enhancers	Brain Inferior Temporal Lobe	brain
39	chr8:111990800-111993400	Weak transcription	Brain Inferior Temporal Lobe	brain
40	chr8:111993400-111993600	Enhancers	Brain Hippocampus Middle	brain
41	chr8:111993400-111993600	Enhancers	Brain Inferior Temporal Lobe	brain
42	chr8:111993600-111994000	Enhancers	Fetal Brain Male	brain
43	chr8:111993600-111995000	Weak transcription	Brain Hippocampus Middle	brain
44	chr8:111993600-111995200	Weak transcription	Brain Inferior Temporal Lobe	brain
45	chr8:111995000-111995200	Flanking Active TSS	Brain Hippocampus Middle	brain
46	chr8:111995000-111995600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr8:111995000-111995600	Active TSS	Brain Cingulate Gyrus	brain
48	chr8:111995200-111995600	Active TSS	Brain Hippocampus Middle	brain
49	chr8:111995200-111995800	Enhancers	Brain Angular Gyrus	brain
50	chr8:111995200-111995800	Active TSS	Brain Inferior Temporal Lobe	brain

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