Variant report

Variant	esv2762764
Chromosome Location	chr8:111973389-112160284
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:840)
CpG islands
(count:183)
Chromatin interactive
region (count:79)
LncRNA
region (count:35)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:840 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

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	ATF1	chr8:112132480-112132510	K562	blood:	n/a	n/a
6	BACH1	chr8:112001137-112001412	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr8:112001168-112001459	K562	blood:	n/a	n/a
8	BATF	chr8:112113181-112113447	GM12878	blood:	n/a	n/a
9	BCL3	chr8:112032257-112032818	K562	blood:	n/a	n/a
10	BCLAF1	chr8:112049253-112049676	K562	blood:	n/a	n/a
11	BCLAF1	chr8:112050664-112051080	K562	blood:	n/a	n/a
12	BCLAF1	chr8:112047895-112049222	K562	blood:	n/a	n/a
13	BCLAF1	chr8:112051891-112052761	K562	blood:	n/a	n/a
14	BCLAF1	chr8:112051085-112051725	K562	blood:	n/a	n/a
15	BCLAF1	chr8:112045287-112045677	K562	blood:	n/a	n/a
16	BHLHE40	chr8:112113324-112113447	K562	blood:	n/a	n/a
17	BRCA1	chr8:112152605-112152831	H1-hESC	embryonic stem cell:	n/a	n/a
18	CBX3	chr8:112052302-112052706	K562	blood:	n/a	n/a
19	CBX3	chr8:112112808-112113129	K562	blood:	n/a	n/a
20	CCNT2	chr8:112098454-112098654	K562	blood:	n/a	n/a
21	CCNT2	chr8:112053174-112053372	K562	blood:	n/a	n/a
22	CCNT2	chr8:112035228-112035538	K562	blood:	n/a	n/a
23	CEBPB	chr8:112044174-112044499	HepG2	liver:	n/a	chr8:112044333-112044344
24	CEBPB	chr8:112152567-112153096	MCF-7	breast:	n/a	n/a
25	CEBPB	chr8:111989225-111989607	MCF-7	breast:	n/a	chr8:111989417-111989430 chr8:111989417-111989428 chr8:111989417-111989430 chr8:111989417-111989428
26	CEBPB	chr8:112054708-112055042	IMR90	lung:	n/a	n/a
27	CEBPB	chr8:112005302-112005679	K562	blood:	n/a	chr8:112005438-112005449
28	CEBPB	chr8:112101875-112101968	K562	blood:	n/a	chr8:112101947-112101958
29	CEBPB	chr8:112054718-112055073	A549	lung:	n/a	n/a
30	CEBPB	chr8:112003396-112003657	A549	lung:	n/a	chr8:112003559-112003570 chr8:112003465-112003477
31	CEBPB	chr8:111982078-111982135	HepG2	liver:	n/a	chr8:111982113-111982124
32	CEBPB	chr8:112005291-112005662	Hela-S3	cervix:	n/a	chr8:112005438-112005449
33	CEBPB	chr8:112005347-112005579	HepG2	liver:	n/a	chr8:112005438-112005449
34	CEBPB	chr8:112101790-112102112	HepG2	liver:	n/a	chr8:112101947-112101958
35	CEBPB	chr8:112005205-112005680	HepG2	liver:	n/a	chr8:112005438-112005449
36	CEBPB	chr8:112005374-112005612	A549	lung:	n/a	chr8:112005438-112005449
37	CEBPB	chr8:112058029-112058214	K562	blood:	n/a	n/a
38	CEBPB	chr8:112005319-112005618	K562	blood:	n/a	chr8:112005438-112005449
39	CEBPB	chr8:112020080-112020285	A549	lung:	n/a	chr8:112020166-112020179 chr8:112020253-112020264 chr8:112020167-112020178 chr8:112020251-112020264 chr8:112020253-112020264
40	CEBPB	chr8:112005299-112005671	HepG2	liver:	n/a	chr8:112005438-112005449
41	CEBPB	chr8:112101778-112102105	H1-hESC	embryonic stem cell:	n/a	chr8:112101947-112101958
42	CEBPB	chr8:112005317-112005565	HepG2	liver:	n/a	chr8:112005438-112005449
43	CEBPB	chr8:112054705-112055080	K562	blood:	n/a	n/a
44	CEBPB	chr8:112020022-112020325	IMR90	lung:	n/a	chr8:112020166-112020179 chr8:112020253-112020264 chr8:112020167-112020178 chr8:112020251-112020264 chr8:112020253-112020264
45	CEBPB	chr8:111992078-111992115	HepG2	liver:	n/a	n/a
46	CEBPB	chr8:112054880-112054909	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr8:112072418-112072646	HepG2	liver:	n/a	chr8:112072555-112072566 chr8:112072538-112072549
48	CEBPB	chr8:112044195-112044491	K562	blood:	n/a	chr8:112044333-112044344
49	CEBPB	chr8:112004396-112004736	HepG2	liver:	n/a	chr8:112004519-112004532
50	CEBPB	chr8:112152585-112152901	H1-hESC	embryonic stem cell:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:112053356-112053406	BE2_C	brain:	n/a
2	chr8:112053139-112053189	HepG2	liver:	n/a
3	chr8:112052376-112052426	HRCEpiC	kidney:	n/a
4	chr8:112053356-112053406	SKMC	muscle:	n/a
5	chr8:112053356-112053406	HMEC	breast:	n/a
6	chr8:112053356-112053406	PrEC	prostate:	n/a
7	chr8:112053139-112053189	T-47D	breast:	n/a
8	chr8:112053139-112053189	GM12892	blood:	n/a
9	chr8:112052376-112052426	HIPEpiC	eye:	n/a
10	chr8:112052376-112052426	PANC-1	pancreas:	n/a
11	chr8:112053356-112053406	ovcar-3	ovarian:	n/a
12	chr8:112053356-112053406	HAEpiC	amniotic membrane:	n/a
13	chr8:112053356-112053406	LNCaP	prostate:	n/a
14	chr8:112053356-112053406	NHBE	bronchial:	n/a
15	chr8:112053139-112053189	NB4	blood:	n/a
16	chr8:112053356-112053406	BJ	skin:	n/a
17	chr8:112052376-112052426	GM12892	blood:	n/a
18	chr8:112052376-112052426	Hela-S3	cervix:	n/a
19	chr8:112053139-112053189	ProgFib	skin:	n/a
20	chr8:112053139-112053189	HCPEpiC	choroid plexus:	n/a
21	chr8:112053356-112053406	H1-hESC	embryonic stem cell:	embryo
22	chr8:112053356-112053406	Hela-S3	cervix:	n/a
23	chr8:112053139-112053189	PANC-1	pancreas:	n/a
24	chr8:112052376-112052426	HEEpiC	esophagus:	n/a
25	chr8:112053139-112053189	SK-N-SH_RA	brain:	n/a
26	chr8:112053139-112053189	GM06990	blood:	n/a
27	chr8:112053356-112053406	IMR90	lung:	fetal
28	chr8:112053356-112053406	SAEC	small airway:	n/a
29	chr8:112053139-112053189	GM12891	blood:	n/a
30	chr8:112053139-112053189	IMR90	lung:	fetal
31	chr8:112052376-112052426	AG04450	lung:	fetal
32	chr8:112053139-112053189	MCF10A-Er-Src	breast:	n/a
33	chr8:112052376-112052426	ECC-1	luminal epithelium:	n/a
34	chr8:112053356-112053406	RPTEC	kidney:	n/a
35	chr8:112053356-112053406	SK-N-MC	brain:	n/a
36	chr8:112053356-112053406	A549	lung:	n/a
37	chr8:112053356-112053406	HRE	kidney:	n/a
38	chr8:112052376-112052426	BE2_C	brain:	n/a
39	chr8:112053139-112053189	HMEC	breast:	n/a
40	chr8:112052376-112052426	NHDF-neo	bronchial:	n/a
41	chr8:112052376-112052426	IMR90	lung:	fetal
42	chr8:112053139-112053189	H1-hESC	embryonic stem cell:	embryo
43	chr8:112053356-112053406	AG10803	skin:	n/a
44	chr8:112052376-112052426	Jurkat	blood:	n/a
45	chr8:112052376-112052426	SKMC	muscle:	n/a
46	chr8:112053356-112053406	HCPEpiC	choroid plexus:	n/a
47	chr8:112052376-112052426	SAEC	small airway:	n/a
48	chr8:112052376-112052426	RPTEC	kidney:	n/a
49	chr8:112052376-112052426	ovcar-3	ovarian:	n/a
50	chr8:112052376-112052426	Caco-2	colon:	n/a

(count:79 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:112049821..112051426-chr8:112052995..112056257,3	K562	blood:
2	chr8:112123114..112125207-chr8:112128541..112131451,2	K562	blood:
3	chr8:112139232..112142043-chr8:112142133..112144046,2	MCF-7	breast:
4	chr8:112112298..112113981-chr8:112264995..112266040,10	MCF-7	breast:
5	chr8:112054463..112057447-chr8:112061238..112063289,2	K562	blood:
6	chr8:112152211..112153851-chr8:112248272..112249455,10	MCF-7	breast:
7	chr8:111986722..111988349-chr8:112001568..112003641,2	K562	blood:
8	chr8:112045873..112047633-chr8:112047967..112049827,3	K562	blood:
9	chr8:112113576..112114171-chr8:112248201..112249138,2	MCF-7	breast:
10	chr8:112020517..112022084-chr8:112022778..112025177,2	K562	blood:
11	chr8:112073611..112075207-chr8:112079150..112081817,2	MCF-7	breast:
12	chr8:112069491..112071465-chr8:112075168..112076781,2	K562	blood:
13	chr8:112069491..112071465-chr8:112075168..112076781,2	K562	blood:
14	chr8:112121761..112124184-chr8:112126207..112129085,2	K562	blood:
15	chr8:112023343..112027872-chr8:112028215..112031579,4	K562	blood:
16	chr8:112142087..112143993-chr8:112151164..112153566,2	MCF-7	breast:
17	chr8:111977359..111979519-chr8:111986099..111987901,2	K562	blood:
18	chr8:112121761..112124184-chr8:112126207..112129085,2	K562	blood:
19	chr8:112037306..112039469-chr8:112041170..112043078,2	K562	blood:
20	chr8:111877803..111878676-chr8:112126153..112126932,3	MCF-7	breast:
21	chr8:112052147..112053672-chr8:112062800..112065119,2	K562	blood:
22	chr8:112152245..112153161-chr8:112248220..112248923,2	MCF-7	breast:
23	chr8:112050824..112052774-chr8:112058514..112060198,2	K562	blood:
24	chr8:112127583..112130124-chr8:112133579..112135146,2	MCF-7	breast:
25	chr1:120421655..120422591-chr8:112129482..112130279,2	MCF-7	breast:
26	chr8:112001101..112002648-chr8:112002795..112004747,2	K562	blood:
27	chr8:112024408..112026830-chr8:112028447..112030493,2	K562	blood:
28	chr8:112127583..112130124-chr8:112133579..112135146,2	MCF-7	breast:
29	chr5:173612522..173613033-chr8:112023628..112024312,2	MCF-7	breast:
30	chr8:112049920..112051426-chr8:112052995..112055202,2	K562	blood:
31	chr8:112020517..112022084-chr8:112022778..112025177,2	K562	blood:
32	chr8:112001101..112002648-chr8:112002795..112004747,2	K562	blood:
33	chr8:112092554..112095223-chr8:112096856..112098486,2	MCF-7	breast:
34	chr8:112112573..112113471-chr8:121617637..121618420,2	MCF-7	breast:
35	chr8:112040792..112044019-chr8:112049363..112052232,3	K562	blood:
36	chr8:112045873..112047633-chr8:112047967..112049827,3	K562	blood:
37	chr8:112152351..112153276-chr8:112265083..112266006,7	MCF-7	breast:
38	chr8:112115345..112116966-chr8:112124670..112126786,2	MCF-7	breast:
39	chr8:111905363..111907255-chr8:112045592..112048412,2	K562	blood:
40	chr8:112152279..112153172-chr8:112264812..112266234,7	MCF-7	breast:
41	chr8:112046473..112049277-chr8:112050883..112054393,4	K562	blood:
42	chr8:112154689..112157253-chr8:112157958..112160941,2	MCF-7	breast:
43	chr8:112048936..112050603-chr8:112056318..112058671,2	K562	blood:
44	chr8:112047893..112049980-chr8:112071535..112074858,3	K562	blood:
45	chr8:111986722..111988349-chr8:112001568..112003641,2	K562	blood:
46	chr8:112052147..112053672-chr8:112062800..112065119,2	K562	blood:
47	chr8:111948692..111950464-chr8:111998456..112000368,2	MCF-7	breast:
48	chr8:112040792..112044019-chr8:112049363..112052232,3	K562	blood:
49	chr8:112092554..112095223-chr8:112096856..112098486,2	MCF-7	breast:
50	chr8:112051929..112053704-chr8:112063619..112066974,3	K562	blood:

(count:35 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 3750 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:3750 , 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	rs10955554	chr8:111973389-111973390	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs7826449	chr8:111973398-111973399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs574900111	chr8:111973461-111973462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs540702462	chr8:111973472-111973473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs560546829	chr8:111973497-111973498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs10542012	chr8:111973503-111973504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs74928347	chr8:111973504-111973505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs201087619	chr8:111973509-111973510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs370129664	chr8:111973510-111973511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs568336704	chr8:111973534-111973535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs532532630	chr8:111973601-111973602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs139541509	chr8:111973619-111973620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs562988926	chr8:111973681-111973682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs149681964	chr8:111973710-111973711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs548612772	chr8:111973731-111973732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs184407180	chr8:111973774-111973775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs533567537	chr8:111973777-111973778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs7462681	chr8:111973838-111973839	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs576815059	chr8:111973863-111973864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs570200341	chr8:111973872-111973873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs539514147	chr8:111973896-111973897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs368302483	chr8:111974033-111974034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs539203589	chr8:111974181-111974182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs190097308	chr8:111974230-111974231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs374801308	chr8:111974244-111974245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs13280135	chr8:111974285-111974286	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs555720335	chr8:111974310-111974311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs560313999	chr8:111974314-111974315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs181667886	chr8:111974335-111974336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs540616896	chr8:111974348-111974349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs542168899	chr8:111974371-111974372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs560512251	chr8:111974372-111974373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs577266806	chr8:111974376-111974377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs187575837	chr8:111974401-111974402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs13280204	chr8:111974430-111974431	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs563060155	chr8:111974460-111974461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs575520409	chr8:111974489-111974490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs373783678	chr8:111974631-111974632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs531828412	chr8:111974632-111974633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs544030607	chr8:111974701-111974702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs548447755	chr8:111974707-111974708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs190383968	chr8:111974765-111974766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs528015812	chr8:111974771-111974772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs546982743	chr8:111974778-111974779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs570115334	chr8:111974787-111974788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs533001313	chr8:111974815-111974816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs549625070	chr8:111974827-111974828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs569804056	chr8:111974869-111974870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs62520698	chr8:111974969-111974970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs535272293	chr8:111974980-111974981	Weak transcription	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:166 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:111969200-111979600	Weak transcription	K562	blood
2	chr8:111977800-111978200	Enhancers	Brain Substantia Nigra	brain
3	chr8:111978000-111978400	Enhancers	Fetal Brain Male	brain
4	chr8:111978200-111989400	Weak transcription	Brain Substantia Nigra	brain
5	chr8:111984200-111984800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr8:111989200-111989800	Enhancers	Brain Cingulate Gyrus	brain
7	chr8:111989400-111989600	Enhancers	Brain Hippocampus Middle	brain
8	chr8:111989400-111990000	Enhancers	Brain Substantia Nigra	brain
9	chr8:111989800-111993400	Weak transcription	Brain Hippocampus Middle	brain
10	chr8:111989800-111995000	Weak transcription	Brain Cingulate Gyrus	brain
11	chr8:111990000-111995200	Weak transcription	Brain Substantia Nigra	brain
12	chr8:111990400-111990600	Enhancers	Brain Inferior Temporal Lobe	brain
13	chr8:111990800-111993400	Weak transcription	Brain Inferior Temporal Lobe	brain
14	chr8:111993400-111993600	Enhancers	Brain Hippocampus Middle	brain
15	chr8:111993400-111993600	Enhancers	Brain Inferior Temporal Lobe	brain
16	chr8:111993600-111994000	Enhancers	Fetal Brain Male	brain
17	chr8:111993600-111995000	Weak transcription	Brain Hippocampus Middle	brain
18	chr8:111993600-111995200	Weak transcription	Brain Inferior Temporal Lobe	brain
19	chr8:111995000-111995200	Flanking Active TSS	Brain Hippocampus Middle	brain
20	chr8:111995000-111995600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr8:111995000-111995600	Active TSS	Brain Cingulate Gyrus	brain
22	chr8:111995200-111995600	Active TSS	Brain Hippocampus Middle	brain
23	chr8:111995200-111995800	Enhancers	Brain Angular Gyrus	brain
24	chr8:111995200-111995800	Active TSS	Brain Inferior Temporal Lobe	brain
25	chr8:111995200-111995800	Enhancers	Brain Substantia Nigra	brain
26	chr8:111995600-111995800	Flanking Active TSS	Brain Hippocampus Middle	brain
27	chr8:111995600-112009200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr8:112003400-112004600	Enhancers	HepG2	liver
29	chr8:112004600-112005000	Enhancers	Brain Substantia Nigra	brain
30	chr8:112004600-112005400	Flanking Active TSS	HepG2	liver
31	chr8:112004800-112005000	Enhancers	Brain Hippocampus Middle	brain
32	chr8:112005000-112006800	Weak transcription	Brain Hippocampus Middle	brain
33	chr8:112006800-112008600	Enhancers	Brain Hippocampus Middle	brain
34	chr8:112007000-112007800	Enhancers	Brain Inferior Temporal Lobe	brain
35	chr8:112007200-112007400	Enhancers	Brain Cingulate Gyrus	brain
36	chr8:112007400-112008400	Weak transcription	Brain Cingulate Gyrus	brain
37	chr8:112007800-112008400	Weak transcription	Brain Inferior Temporal Lobe	brain
38	chr8:112008200-112008400	Enhancers	Brain Angular Gyrus	brain
39	chr8:112008200-112008800	Enhancers	Brain Anterior Caudate	brain
40	chr8:112008400-112008600	Enhancers	Brain Cingulate Gyrus	brain
41	chr8:112008400-112008600	Enhancers	Brain Inferior Temporal Lobe	brain
42	chr8:112008400-112009800	Weak transcription	Brain Angular Gyrus	brain
43	chr8:112008600-112009000	Weak transcription	Brain Cingulate Gyrus	brain
44	chr8:112008600-112009600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr8:112008600-112009600	Weak transcription	Brain Hippocampus Middle	brain
46	chr8:112008800-112009800	Weak transcription	Brain Anterior Caudate	brain
47	chr8:112009000-112009400	Active TSS	Brain Cingulate Gyrus	brain
48	chr8:112009000-112009400	Enhancers	Fetal Heart	heart
49	chr8:112009200-112009600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr8:112009400-112010000	Enhancers	Brain Cingulate Gyrus	brain

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