Variant report

Variant	nsv891294
Chromosome Location	chr8:111754075-112163801
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2245)
CpG islands
(count:610)
Chromatin interactive
region (count:136)
LncRNA
region (count:39)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2245 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

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	chr8:111927195-111927263	K562	blood:	n/a	n/a
3	ARID3A	chr8:111930749-111931038	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:111860419-111860636	K562	blood:	n/a	n/a
5	ARID3A	chr8:111844706-111844955	HepG2	liver:	n/a	n/a
6	ARID3A	chr8:111842727-111843064	K562	blood:	n/a	n/a
7	ARID3A	chr8:111861128-111861289	K562	blood:	n/a	n/a
8	ARID3A	chr8:112055951-112056163	K562	blood:	n/a	n/a
9	ARID3A	chr8:111842737-111843081	HepG2	liver:	n/a	n/a
10	ARID3A	chr8:111844737-111844834	K562	blood:	n/a	n/a
11	ARID3A	chr8:111860272-111860903	HepG2	liver:	n/a	chr8:111860332-111860348
12	ATF1	chr8:112132480-112132510	K562	blood:	n/a	n/a
13	ATF1	chr8:111875900-111876067	K562	blood:	n/a	n/a
14	ATF1	chr8:111804441-111804627	K562	blood:	n/a	n/a
15	ATF1	chr8:111906691-111907234	K562	blood:	n/a	n/a
16	ATF1	chr8:112055891-112056208	K562	blood:	n/a	n/a
17	ATF1	chr8:112052514-112052777	K562	blood:	n/a	n/a
18	ATF2	chr8:111758640-111758925	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF2	chr8:112162891-112163440	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF2	chr8:111758671-111758920	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF2	chr8:112162917-112163564	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF3	chr8:111860291-111860669	K562	blood:	n/a	n/a
23	BACH1	chr8:112001168-112001459	K562	blood:	n/a	n/a
24	BACH1	chr8:111907020-111907275	K562	blood:	n/a	n/a
25	BACH1	chr8:111914552-111914921	K562	blood:	n/a	chr8:111914731-111914745
26	BACH1	chr8:111914556-111914922	H1-hESC	embryonic stem cell:	n/a	chr8:111914731-111914745
27	BACH1	chr8:112001137-112001412	H1-hESC	embryonic stem cell:	n/a	n/a
28	BATF	chr8:112113181-112113447	GM12878	blood:	n/a	n/a
29	BATF	chr8:111860419-111860570	GM12878	blood:	n/a	chr8:111860544-111860554
30	BATF	chr8:111887241-111887473	GM12878	blood:	n/a	chr8:111887372-111887383 chr8:111887369-111887379 chr8:111887386-111887397
31	BATF	chr8:111887230-111887546	GM12878	blood:	n/a	chr8:111887372-111887383 chr8:111887369-111887379 chr8:111887386-111887397
32	BCL11A	chr8:112162999-112163239	H1-hESC	embryonic stem cell:	n/a	n/a
33	BCL11A	chr8:111758677-111758916	H1-hESC	embryonic stem cell:	n/a	n/a
34	BCL11A	chr8:111758735-111758917	H1-hESC	embryonic stem cell:	n/a	n/a
35	BCL11A	chr8:112162971-112163355	H1-hESC	embryonic stem cell:	n/a	n/a
36	BCL3	chr8:112032257-112032818	K562	blood:	n/a	n/a
37	BCLAF1	chr8:112050664-112051080	K562	blood:	n/a	n/a
38	BCLAF1	chr8:112051085-112051725	K562	blood:	n/a	n/a
39	BCLAF1	chr8:112049253-112049676	K562	blood:	n/a	n/a
40	BCLAF1	chr8:112047895-112049222	K562	blood:	n/a	n/a
41	BCLAF1	chr8:112051891-112052761	K562	blood:	n/a	n/a
42	BCLAF1	chr8:112045287-112045677	K562	blood:	n/a	n/a
43	BHLHE40	chr8:112113324-112113447	K562	blood:	n/a	n/a
44	BHLHE40	chr8:111842552-111842735	K562	blood:	n/a	n/a
45	BHLHE40	chr8:111906788-111907219	K562	blood:	n/a	n/a
46	BHLHE40	chr8:111927453-111927498	GM12878	blood:	n/a	n/a
47	BRCA1	chr8:112152605-112152831	H1-hESC	embryonic stem cell:	n/a	n/a
48	BRCA1	chr8:111880545-111880672	Hela-S3	cervix:	n/a	n/a
49	BRCA1	chr8:111906219-111906223	HepG2	liver:	n/a	n/a
50	BRCA1	chr8:111846598-111846609	HepG2	liver:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:111835043-111835093	HL-60	blood:	n/a
2	chr8:111835043-111835093	MCF10A-Er-Src	breast:	n/a
3	chr8:112053139-112053189	MCF-7	breast:	n/a
4	chr8:111834906-111834956	SK-N-SH_RA	brain:	n/a
5	chr8:111834906-111834956	HCM	heart:	n/a
6	chr8:112053139-112053189	SK-N-MC	brain:	n/a
7	chr8:111834752-111834802	HL-60	blood:	n/a
8	chr8:112053356-112053406	NT2-D1	testis:	n/a
9	chr8:112053139-112053189	HEEpiC	esophagus:	n/a
10	chr8:111834776-111834826	NB4	blood:	n/a
11	chr8:112053356-112053406	NHDF-neo	bronchial:	n/a
12	chr8:112052376-112052426	HRPEpiC	eye:	n/a
13	chr8:111847388-111847438	HMEC	breast:	n/a
14	chr8:111834776-111834826	H1-hESC	embryonic stem cell:	embryo
15	chr8:111835043-111835093	IMR90	lung:	fetal
16	chr8:112052376-112052426	SK-N-SH	brain:	n/a
17	chr8:112052376-112052426	SAEC	small airway:	n/a
18	chr8:112053139-112053189	Hepatocyte	liver:	n/a
19	chr8:112053356-112053406	HCT-116	colon:	n/a
20	chr8:112163550-112163600	AG10803	skin:	n/a
21	chr8:112053356-112053406	HUVEC	blood vessel:	n/a
22	chr8:111834906-111834956	HUVEC	blood vessel:	n/a
23	chr8:111834752-111834802	HUVEC	blood vessel:	n/a
24	chr8:111906503-111906553	HUVEC	blood vessel:	n/a
25	chr8:111847388-111847438	SK-N-SH_RA	brain:	n/a
26	chr8:111906503-111906553	AG10803	skin:	n/a
27	chr8:112053356-112053406	ovcar-3	ovarian:	n/a
28	chr8:112053139-112053189	AG09309	skin:	n/a
29	chr8:111906503-111906553	HMEC	breast:	n/a
30	chr8:111906503-111906553	SK-N-SH_RA	brain:	n/a
31	chr8:111834906-111834956	HCPEpiC	choroid plexus:	n/a
32	chr8:111834776-111834826	GM06990	blood:	n/a
33	chr8:112053139-112053189	LNCaP	prostate:	n/a
34	chr8:111847388-111847438	HPAEpiC	pulmonary alveolar:	n/a
35	chr8:111834906-111834956	NHDF-neo	bronchial:	n/a
36	chr8:111835043-111835093	SKMC	muscle:	n/a
37	chr8:111834776-111834826	Hela-S3	cervix:	n/a
38	chr8:112163550-112163600	A549	lung:	n/a
39	chr8:111847388-111847438	AG09319	gingival:	n/a
40	chr8:111834752-111834802	PFSK-1	brain:	n/a
41	chr8:111834776-111834826	ovcar-3	ovarian:	n/a
42	chr8:111835043-111835093	GM06990	blood:	n/a
43	chr8:112053356-112053406	GM12891	blood:	n/a
44	chr8:111834776-111834826	LNCaP	prostate:	n/a
45	chr8:112053356-112053406	SK-N-SH	brain:	n/a
46	chr8:111834752-111834802	PANC-1	pancreas:	n/a
47	chr8:111834906-111834956	HIPEpiC	eye:	n/a
48	chr8:111847388-111847438	CMK	blood:	n/a
49	chr8:112053356-112053406	SK-N-SH_RA	brain:	n/a
50	chr8:111834776-111834826	SAEC	small airway:	n/a

(count:136 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr8:111924377..111926908-chr8:111953183..111955700,2	K562	blood:
2	chr8:112152351..112153276-chr8:112265083..112266006,7	MCF-7	breast:
3	chr8:112026713..112028384-chr8:112038537..112040451,2	K562	blood:
4	chr8:112151809..112153959-chr8:112263594..112266459,2	MCF-7	breast:
5	chr8:112037306..112039469-chr8:112041170..112043078,2	K562	blood:
6	chr8:111948692..111950464-chr8:111998456..112000368,2	MCF-7	breast:
7	chr8:111811884..111813878-chr8:111822855..111824615,2	K562	blood:
8	chr8:112154689..112157253-chr8:112157958..112160941,2	MCF-7	breast:
9	chr8:111781609..111784016-chr8:111789603..111791637,2	MCF-7	breast:
10	chr8:111744937..111746990-chr8:111753666..111755908,2	K562	blood:
11	chr8:111913749..111916185-chr8:111918003..111920287,2	MCF-7	breast:
12	chr8:111993072..111993615-chr8:112265097..112265675,2	MCF-7	breast:
13	chr8:112115345..112116966-chr8:112124670..112126786,2	MCF-7	breast:
14	chr8:111853597..111856569-chr8:111856769..111860452,3	MCF-7	breast:
15	chr8:111924377..111926908-chr8:111953183..111955700,2	K562	blood:
16	chr8:111877768..111878423-chr8:111945734..111946406,2	MCF-7	breast:
17	chr8:111365308..111365953-chr8:111842805..111843518,2	MCF-7	breast:
18	chr8:111986722..111988349-chr8:112001568..112003641,2	K562	blood:
19	chr8:112049821..112051426-chr8:112052995..112056257,3	K562	blood:
20	chr8:111780743..111782594-chr8:111785721..111788222,2	MCF-7	breast:
21	chr8:112133641..112134299-chr9:13359583..13360482,2	MCF-7	breast:
22	chr8:112046473..112049277-chr8:112050883..112054393,4	K562	blood:
23	chr8:112051929..112053704-chr8:112063619..112066974,3	K562	blood:
24	chr8:111952441..111954881-chr8:111958633..111961171,2	K562	blood:
25	chr8:111905656..111907856-chr8:111909688..111913737,4	K562	blood:
26	chr8:112112155..112113418-chr8:112247960..112249178,7	MCF-7	breast:
27	chr8:112045873..112047633-chr8:112047967..112049827,3	K562	blood:
28	chr8:111977359..111979519-chr8:111986099..111987901,2	K562	blood:
29	chr8:112037306..112039469-chr8:112041170..112043078,2	K562	blood:
30	chr8:111877768..111878423-chr8:111945734..111946406,2	MCF-7	breast:
31	chr8:112069491..112071465-chr8:112075168..112076781,2	K562	blood:
32	chr8:112139232..112142043-chr8:112142133..112144046,2	MCF-7	breast:
33	chr8:111877803..111878676-chr8:112126153..112126932,3	MCF-7	breast:
34	chr8:112052147..112053672-chr8:112062800..112065119,2	K562	blood:
35	chr8:111913749..111916185-chr8:111918003..111920287,2	MCF-7	breast:
36	chr8:111986722..111988349-chr8:112001568..112003641,2	K562	blood:
37	chr8:111799556..111802962-chr8:111805139..111808019,3	MCF-7	breast:
38	chr8:111870941..111873511-chr8:111873961..111876570,2	K562	blood:
39	chr1:225202258..225204234-chr8:111898982..111900583,2	MCF-7	breast:
40	chr5:173612522..173613033-chr8:112023628..112024312,2	MCF-7	breast:
41	chr8:112142087..112143993-chr8:112151164..112153566,2	MCF-7	breast:
42	chr8:112024408..112026830-chr8:112028447..112030493,2	K562	blood:
43	chr8:111365378..111366118-chr8:111834050..111834594,2	MCF-7	breast:
44	chr8:111855787..111857322-chr8:111859376..111860898,2	MCF-7	breast:
45	chr8:111877803..111878653-chr8:112126153..112126716,2	MCF-7	breast:
46	chr8:112069491..112071465-chr8:112075168..112076781,2	K562	blood:
47	chr8:112048936..112050603-chr8:112056318..112058671,2	K562	blood:
48	chr8:112040792..112044019-chr8:112049363..112052232,3	K562	blood:
49	chr8:111918636..111921932-chr8:111925930..111928582,3	K562	blood:
50	chr8:112001101..112002648-chr8:112002795..112004747,2	K562	blood:

(count:39 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-422N16.3.1-3	chr8:111779092-111779145	ENSG00000253717
2	lnc-KCNV1-7	chr8:112108711-112108928	l_3667_chr8:112084787-112108928_brain
3	lnc-KCNV1-2	chr8:112015643-112015679	ENSG00000253877
4	lnc-KCNV1-2	chr8:112017759-112017878	ENSG00000253877
5	lnc-KCNV1-2	chr8:111994744-111995369	XLOC_007182
6	lnc-KCNV1-7	chr8:112086929-112087054	l_3667_chr8:112084787-112108928_brain
7	lnc-KCNV1-7	chr8:112086066-112086174	l_3667_chr8:112084787-112108928_brain
8	lnc-KCNV1-2	chr8:112015643-112015679	XLOC_007182
9	lnc-RP11-422N16.3.1-6	chr8:112002113-112002710	NONHSAT128319
10	lnc-KCNV1-2	chr8:111995179-111995369	ENSG00000253877
11	lnc-KCNV1-2	chr8:111949919-111949956	ENSG00000253877
12	lnc-KCNV1-2	chr8:112016890-112016998	XLOC_007182
13	lnc-KCNV1-2	chr8:112039535-112039621	ENSG00000253877
14	lnc-KCNV1-2	chr8:112015643-112015679	ENSG00000253877
15	lnc-RP11-422N16.3.1-6	chr8:112000448-112001045	FPKM1_group_31989_transcript_3
16	lnc-KCNV1-2	chr8:112027133-112027261	ENSG00000253877
17	lnc-KCNV1-2	chr8:112015643-112015679	XLOC_007182
18	lnc-KCNV1-2	chr8:112016890-112016998	ENSG00000253877
19	lnc-RP11-422N16.3.1-6	chr8:112000263-112000924	FPKM1_group_31989_transcript_3
20	lnc-KCNV1-2	chr8:112039535-112039662	ENSG00000253877
21	lnc-KCNV1-2	chr8:112015643-112015679	XLOC_007182
22	lnc-KCNV1-2	chr8:112016890-112016998	ENSG00000253877
23	lnc-CSMD3-3	chr8:112128764-112128829	ENSG00000253103
24	lnc-KCNV1-2	chr8:112017759-112017878	ENSG00000253877
25	lnc-KCNV1-7	chr8:112096343-112096437	l_3667_chr8:112084787-112108928_brain
26	lnc-KCNV1-2	chr8:112017759-112017878	XLOC_007182
27	lnc-KCNV1-2	chr8:111993626-111995369	XLOC_007182
28	lnc-RP11-422N16.3.1-6	chr8:112000263-112000924	NONHSAT128319
29	lnc-KCNV1-2	chr8:111991098-111995369	XLOC_007182
30	lnc-RP11-422N16.3.1-3	chr8:111784567-111784988	ENSG00000253717
31	lnc-CSMD3-3	chr8:112111190-112111368	ENSG00000253103
32	lnc-KCNV1-2	chr8:112017759-112017878	XLOC_007182
33	lnc-KCNV1-2	chr8:112039535-112039752	XLOC_007182
34	lnc-KCNV1-5	chr8:111821623-111822123	NONHSAT128312
35	lnc-CSMD3-3	chr8:112125661-112125749	ENSG00000253103
36	lnc-KCNV1-2	chr8:112039535-112039752	XLOC_007182
37	lnc-KCNV1-2	chr8:112016890-112016917	XLOC_007182
38	lnc-KCNV1-2	chr8:112039535-112039641	XLOC_007182
39	lnc-KCNV1-7	chr8:112084788-112084855	l_3667_chr8:112084787-112108928_brain

No data

Variant related genes	Relation type
ENSG00000253994	TF binding region
ENSG00000253877	TF binding region
ENSG00000254241	TF binding region
ENSG00000253717	TF binding region
ENSG00000253994	CpG island
ENSG00000253877	CpG island
ENSG00000254241	CpG island
ENSG00000253717	CpG island
ENSG00000253877	chromatin interactions
ENSG00000253103	chromatin interactions
ENSG00000253717	chromatin interactions
ZEB2	miRNA target sites
TFRC	miRNA target sites
CDC42	miRNA target sites
ZFPM2	miRNA target sites
DNMT1	miRNA target sites
AADACL3	miRNA target sites

Extended variants
information (count: 8874 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:8874 , 50 per page) page: 1 2 3 4 5 6 7 ... 178

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs140017648	chr8:111758414-111758415	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs373795395	chr8:111758483-111758484	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs193127583	chr8:111758489-111758490	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs185625130	chr8:111758505-111758506	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs551294215	chr8:111758510-111758511	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs571382934	chr8:111758526-111758527	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs536768712	chr8:111758538-111758539	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs555522921	chr8:111758572-111758573	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs569133067	chr8:111758624-111758625	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs189229948	chr8:111758627-111758628	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs567304355	chr8:111758631-111758632	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs536244203	chr8:111758639-111758640	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs553750442	chr8:111758652-111758653	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs573461762	chr8:111758675-111758676	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs539279702	chr8:111758719-111758720	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs558901099	chr8:111758784-111758785	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs6997576	chr8:111758818-111758819	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs544330090	chr8:111758821-111758822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs561033374	chr8:111758822-111758823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs553501501	chr8:111758863-111758864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs371923399	chr8:111758866-111758867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs540234587	chr8:111758867-111758868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs542875198	chr8:111758908-111758909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs192613278	chr8:111758911-111758912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs184787272	chr8:111758933-111758934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs188523194	chr8:111758940-111758941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs564959623	chr8:111758974-111758975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs376335563	chr8:111759019-111759020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs371057676	chr8:111759020-111759021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs181243167	chr8:111759046-111759047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs36015683	chr8:111759080-111759081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs557469571	chr8:111759167-111759168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs186279506	chr8:111759245-111759246	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs529768722	chr8:111759253-111759254	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs546629709	chr8:111759267-111759268	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs566428859	chr8:111759298-111759299	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs538985798	chr8:111759305-111759306	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs559184708	chr8:111759320-111759321	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs188997040	chr8:111759368-111759369	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs182272707	chr8:111759378-111759379	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs554692778	chr8:111759381-111759382	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs34858925	chr8:111759391-111759392	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs200930310	chr8:111759422-111759423	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs36001884	chr8:111759424-111759425	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs4273835	chr8:111759490-111759491	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs540293810	chr8:111759517-111759518	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs553897579	chr8:111759553-111759554	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs577146507	chr8:111759634-111759635	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs149847739	chr8:111759661-111759662	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs145835069	chr8:111759685-111759686	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

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
early-passage human iPS cells	21368824	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:526 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:111758400-111758800	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr8:111758800-111759200	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr8:111759200-111759800	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr8:111759400-111759800	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr8:111764000-111764600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr8:111764200-111764800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr8:111768400-111769600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr8:111769200-111770000	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr8:111769400-111769800	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr8:111769400-111769800	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr8:111769400-111769800	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr8:111772200-111772600	Active TSS	Aorta	Aorta
13	chr8:111784800-111785600	Enhancers	Fetal Intestine Small	intestine
14	chr8:111788600-111826200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr8:111791600-111792000	Active TSS	Primary hematopoietic stem cells	blood
16	chr8:111802400-111802800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr8:111802800-111803200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr8:111803200-111804000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr8:111803200-111804400	Enhancers	Fetal Intestine Large	intestine
20	chr8:111803400-111804200	Enhancers	Fetal Intestine Small	intestine
21	chr8:111804000-111804400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr8:111814600-111815200	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr8:111814600-111815200	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr8:111814800-111815400	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr8:111815000-111815200	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr8:111815000-111815400	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr8:111818600-111818800	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr8:111818600-111819600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr8:111818800-111819400	Enhancers	Adipose Nuclei	Adipose
30	chr8:111818800-111819800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr8:111818800-111821000	Weak transcription	HUES64 Cell Line	embryonic stem cell
32	chr8:111820200-111821000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr8:111820600-111821000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr8:111821000-111821400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr8:111821000-111821600	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr8:111821000-111822400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr8:111821400-111822200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr8:111821600-111822000	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr8:111821600-111822800	Weak transcription	HUES64 Cell Line	embryonic stem cell
40	chr8:111822400-111822800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr8:111822600-111823200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr8:111822800-111823000	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr8:111826200-111826400	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr8:111834600-111835000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr8:111835000-111842600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr8:111839600-111839800	Enhancers	H9 Cell Line	embryonic stem cell
47	chr8:111840000-111840400	Enhancers	Fetal Lung	lung
48	chr8:111840400-111847200	Weak transcription	Fetal Lung	lung
49	chr8:111841800-111842200	Enhancers	H9 Cell Line	embryonic stem cell
50	chr8:111841800-111842400	Enhancers	ES-I3 Cell Line	embryonic stem cell

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