Variant report

Variant	esv3377304
Chromosome Location	chr8:53873441-54380875
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2269)
CpG islands
(count:1407)
Chromatin interactive
region (count:51)
LncRNA
region (count:31)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2269 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:53878484-53878808	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:53878433-53878817	K562	blood:	n/a	n/a
3	ATF1	chr8:54244951-54244960	K562	blood:	n/a	n/a
4	ATF2	chr8:54277849-54278369	GM12878	blood:	n/a	n/a
5	ATF2	chr8:54158015-54158946	GM12878	blood:	n/a	n/a
6	ATF2	chr8:53909866-53910228	GM12878	blood:	n/a	n/a
7	ATF2	chr8:54277911-54278322	GM12878	blood:	n/a	n/a
8	ATF2	chr8:54108078-54108544	GM12878	blood:	n/a	n/a
9	BACH1	chr8:54256653-54256931	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr8:54199377-54199659	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr8:54326446-54326519	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr8:54163314-54163469	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr8:54313831-54313834	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr8:54172022-54172267	GM12878	blood:	n/a	chr8:54172159-54172169 chr8:54172163-54172173 chr8:54172158-54172169
15	BATF	chr8:54108183-54108518	GM12878	blood:	n/a	n/a
16	BATF	chr8:53909878-53910230	GM12878	blood:	n/a	chr8:53910027-53910037 chr8:53910026-53910037
17	BATF	chr8:54279973-54280244	GM12878	blood:	n/a	n/a
18	BATF	chr8:54158157-54158741	GM12878	blood:	n/a	n/a
19	BATF	chr8:54148656-54148866	GM12878	blood:	n/a	n/a
20	BATF	chr8:54158025-54158871	GM12878	blood:	n/a	n/a
21	BATF	chr8:54148673-54148936	GM12878	blood:	n/a	n/a
22	BATF	chr8:54108091-54108535	GM12878	blood:	n/a	n/a
23	BATF	chr8:54277918-54278334	GM12878	blood:	n/a	n/a
24	BATF	chr8:54278559-54278861	GM12878	blood:	n/a	n/a
25	BATF	chr8:54277881-54278354	GM12878	blood:	n/a	n/a
26	BATF	chr8:53932574-53932770	GM12878	blood:	n/a	n/a
27	BATF	chr8:54278537-54278911	GM12878	blood:	n/a	n/a
28	BCL11A	chr8:54279973-54280203	GM12878	blood:	n/a	n/a
29	BCL11A	chr8:54280737-54280907	GM12878	blood:	n/a	n/a
30	BCL11A	chr8:54279973-54280176	GM12878	blood:	n/a	n/a
31	BCL11A	chr8:54277858-54278335	GM12878	blood:	n/a	chr8:54278095-54278104
32	BCL11A	chr8:53909839-53910302	GM12878	blood:	n/a	chr8:53910131-53910140
33	BCL11A	chr8:54158068-54158714	GM12878	blood:	n/a	n/a
34	BCL11A	chr8:54277973-54278265	GM12878	blood:	n/a	chr8:54278095-54278104
35	BCL11A	chr8:53909858-53910582	GM12878	blood:	n/a	chr8:53910131-53910140 chr8:53910301-53910310
36	BCL3	chr8:54271942-54272209	GM12878	blood:	n/a	n/a
37	BCL3	chr8:54195005-54195297	GM12878	blood:	n/a	n/a
38	BCL3	chr8:54271967-54272188	GM12878	blood:	n/a	n/a
39	BCL3	chr8:54194789-54195390	GM12878	blood:	n/a	n/a
40	BCLAF1	chr8:54158074-54158952	GM12878	blood:	n/a	n/a
41	BHLHE40	chr8:53917469-53917491	K562	blood:	n/a	n/a
42	BHLHE40	chr8:54077456-54077710	GM12878	blood:	n/a	n/a
43	BHLHE40	chr8:54077445-54077674	K562	blood:	n/a	n/a
44	BHLHE40	chr8:53909862-53910567	GM12878	blood:	n/a	n/a
45	BHLHE40	chr8:53883301-53883728	GM12878	blood:	n/a	n/a
46	BHLHE40	chr8:53884307-53884596	GM12878	blood:	n/a	n/a
47	BRCA1	chr8:53883776-53883853	H1-hESC	embryonic stem cell:	n/a	n/a
48	BRCA1	chr8:54256884-54257130	Hela-S3	cervix:	n/a	n/a
49	BRCA1	chr8:54199428-54199587	H1-hESC	embryonic stem cell:	n/a	n/a
50	BRCA1	chr8:53967252-53967345	GM12878	blood:	n/a	n/a

(count:1407 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:54154426-54154476	GM12892	blood:	n/a
2	chr8:54142212-54142262	SK-N-SH_RA	brain:	n/a
3	chr8:54164296-54164346	HUVEC	blood vessel:	n/a
4	chr8:54164374-54164424	PANC-1	pancreas:	n/a
5	chr8:54154426-54154476	GM12892	blood:	n/a
6	chr8:54142212-54142262	SK-N-SH_RA	brain:	n/a
7	chr8:54164296-54164346	HUVEC	blood vessel:	n/a
8	chr8:54164374-54164424	PANC-1	pancreas:	n/a
9	chr8:54142009-54142059	A549	lung:	n/a
10	chr8:54159889-54159939	HRCEpiC	kidney:	n/a
11	chr8:54164757-54164807	SAEC	small airway:	n/a
12	chr8:54142212-54142262	BE2_C	brain:	n/a
13	chr8:54142009-54142059	NT2-D1	testis:	n/a
14	chr8:54164081-54164131	HCM	heart:	n/a
15	chr8:54164161-54164211	BE2_C	brain:	n/a
16	chr8:54142009-54142059	SK-N-MC	brain:	n/a
17	chr8:54163622-54163672	HIPEpiC	eye:	n/a
18	chr8:54137552-54137602	NHBE	bronchial:	n/a
19	chr8:54164310-54164360	PrEC	prostate:	n/a
20	chr8:54142212-54142262	AG09319	gingival:	n/a
21	chr8:54164442-54164492	HL-60	blood:	n/a
22	chr8:54154528-54154578	GM12892	blood:	n/a
23	chr8:54162969-54163019	PFSK-1	brain:	n/a
24	chr8:54164310-54164360	GM12892	blood:	n/a
25	chr8:54154426-54154476	AG09319	gingival:	n/a
26	chr8:54154426-54154476	Caco-2	colon:	n/a
27	chr8:54159889-54159939	HCT-116	colon:	n/a
28	chr8:54164296-54164346	BE2_C	brain:	n/a
29	chr8:54140771-54140821	Caco-2	colon:	n/a
30	chr8:54164081-54164131	AoSMC	blood vessel:	n/a
31	chr8:54163693-54163743	GM12892	blood:	n/a
32	chr8:54137552-54137602	Caco-2	colon:	n/a
33	chr8:54164442-54164492	PrEC	prostate:	n/a
34	chr8:54164310-54164360	SK-N-MC	brain:	n/a
35	chr8:54165371-54165421	HCF	heart:	n/a
36	chr8:54154489-54154539	GM12892	blood:	n/a
37	chr8:54140771-54140821	A549	lung:	n/a
38	chr8:54164391-54164441	AG10803	skin:	n/a
39	chr8:54164296-54164346	AG10803	skin:	n/a
40	chr8:54154426-54154476	SK-N-MC	brain:	n/a
41	chr8:54168064-54168114	BJ	skin:	n/a
42	chr8:54154528-54154578	ECC-1	luminal epithelium:	n/a
43	chr8:54164161-54164211	SK-N-SH_RA	brain:	n/a
44	chr8:54164051-54164101	BJ	skin:	n/a
45	chr8:54142212-54142262	Caco-2	colon:	n/a
46	chr8:54162969-54163019	SK-N-SH	brain:	n/a
47	chr8:54164442-54164492	BE2_C	brain:	n/a
48	chr8:54163693-54163743	PrEC	prostate:	n/a
49	chr8:54140771-54140821	NB4	blood:	n/a
50	chr8:54140771-54140821	Hepatocyte	liver:	n/a

(count:51 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:54183317..54185825-chr8:54188088..54189770,2	K562	blood:
2	chr8:54159925..54162386-chr8:54168692..54170589,2	K562	blood:
3	chr8:54098132..54100094-chr8:54103558..54106021,2	K562	blood:
4	chr8:54319987..54321896-chr8:54323877..54325521,2	K562	blood:
5	chr8:53963436..53966378-chr8:53966833..53968910,3	K562	blood:
6	chr8:54121078..54124068-chr8:54126518..54128472,2	K562	blood:
7	chr8:54056324..54058341-chr8:54060726..54063007,2	K562	blood:
8	chr8:54095598..54097132-chr8:54099814..54101680,2	K562	blood:
9	chr8:53878320..53879023-chr8:54317254..54317896,3	MCF-7	breast:
10	chr8:53878320..53879023-chr8:54317254..54317896,3	MCF-7	breast:
11	chr8:54143686..54145583-chr8:54146920..54148945,2	K562	blood:
12	chr8:54143686..54145583-chr8:54146920..54148945,2	K562	blood:
13	chr8:54193004..54195448-chr8:54197380..54199028,2	K562	blood:
14	chr8:54031738..54034057-chr8:54034644..54036754,2	K562	blood:
15	chr8:54317487..54319205-chr8:54328127..54329982,2	MCF-7	breast:
16	chr8:54159925..54162386-chr8:54168692..54170589,2	K562	blood:
17	chr8:54062988..54064727-chr8:54068007..54069989,2	K562	blood:
18	chr8:54236248..54239021-chr8:54240226..54242196,2	MCF-7	breast:
19	chr8:53878008..53878947-chr8:55078471..55079402,3	K562	blood:
20	chr8:53939330..53941903-chr8:53942463..53944811,2	MCF-7	breast:
21	chr8:54236248..54239021-chr8:54240226..54242196,2	MCF-7	breast:
22	chr8:54098132..54100094-chr8:54103558..54106021,2	K562	blood:
23	chr8:54056841..54058640-chr8:54061137..54063007,2	K562	blood:
24	chr8:54230692..54232503-chr8:54232952..54235778,2	K562	blood:
25	chr8:53878134..53878972-chr8:54721059..54722142,3	K562	blood:
26	chr8:53963436..53966378-chr8:53966833..53968910,3	K562	blood:
27	chr8:54031738..54034057-chr8:54034644..54036754,2	K562	blood:
28	chr8:54098675..54101243-chr8:54110887..54112724,2	K562	blood:
29	chr8:54317487..54319205-chr8:54328127..54329982,2	MCF-7	breast:
30	chr8:53966830..53968334-chr8:53977318..53980118,2	K562	blood:
31	chr8:54183317..54185825-chr8:54188088..54189770,2	K562	blood:
32	chr8:53966830..53968334-chr8:53977318..53980118,2	K562	blood:
33	chr8:54156472..54161055-chr8:54164094..54168308,5	K562	blood:
34	chr8:54056841..54058640-chr8:54061137..54063007,2	K562	blood:
35	chr8:54147248..54149206-chr8:54604109..54606269,2	MCF-7	breast:
36	chr8:54230692..54232503-chr8:54232952..54235778,2	K562	blood:
37	chr8:53939330..53941903-chr8:53942463..53944811,2	MCF-7	breast:
38	chr8:54056324..54058341-chr8:54060726..54063007,2	K562	blood:
39	chr8:54317343..54318633-chr8:54398864..54399407,3	MCF-7	breast:
40	chr8:54062988..54064727-chr8:54068007..54069989,2	K562	blood:
41	chr8:54094529..54096106-chr8:54115810..54118558,2	K562	blood:
42	chr8:54189481..54190049-chr9:136209967..136210542,2	MCF-7	breast:
43	chr8:53878057..53878612-chr8:54775599..54776413,2	K562	blood:
44	chr8:54095598..54097132-chr8:54099814..54101680,2	K562	blood:
45	chr8:54094529..54096106-chr8:54115810..54118558,2	K562	blood:
46	chr8:54121078..54124068-chr8:54126518..54128472,2	K562	blood:
47	chr8:54098675..54101243-chr8:54110887..54112724,2	K562	blood:
48	chr8:54193004..54195448-chr8:54197380..54199028,2	K562	blood:
49	chr18:13291375..13292050-chr8:53976127..53977109,2	MCF-7	breast:
50	chr8:53878521..53879036-chr8:54398874..54399575,2	MCF-7	breast:

(count:31 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OPRK1-3	chr8:54307910-54308316	NONHSAT126587
2	lnc-NPBWR1-1	chr8:54090131-54090563	ENSG00000254687.1
3	lnc-OPRK1-3	chr8:54333626-54333713	NONHSAT126587
4	lnc-OPRK1-3	chr8:54333626-54333713	NONHSAT126590
5	lnc-OPRK1-3	chr8:54308459-54308506	ENSG00000253369
6	lnc-OPRK1-3	chr8:54334783-54334854	NONHSAT126589
7	lnc-NPBWR1-1	chr8:54090147-54090610	ENSG00000254687.1
8	lnc-OPRK1-3	chr8:54308459-54308541	NONHSAT126587
9	lnc-OPRK1-3	chr8:54308433-54308626	NONHSAT126590
10	lnc-NPBWR1-1	chr8:54155088-54155243	ENSG00000254687.1
11	lnc-OPRK1-2	chr8:54301261-54303432	ENSG00000260484.1
12	lnc-OPRK1-3	chr8:54333626-54333713	NONHSAT126589
13	lnc-OPRK1-3	chr8:54308459-54308626	NONHSAT126589
14	lnc-NPBWR1-1	chr8:54128859-54129064	ENSG00000254687.1
15	lnc-OPRK1-1	chr8:54190698-54190843	XLOC_007082
16	lnc-OPRK1-3	chr8:54312130-54312397	NONHSAT126590
17	lnc-OPRK1-3	chr8:54314040-54314129	NONHSAT126588
18	lnc-NPBWR1-3	chr8:54075401-54075547	NONHSAT126578
19	lnc-OPRK1-3	chr8:54333626-54333730	NONHSAT126588
20	lnc-OPRK1-3	chr8:54312130-54312397	NONHSAT126589
21	lnc-NPBWR1-3	chr8:54074899-54075069	NONHSAT126578
22	lnc-OPRK1-3	chr8:54314040-54314129	NONHSAT126589
23	lnc-OPRK1-3	chr8:54312130-54312397	NONHSAT126588
24	lnc-OPRK1-1	chr8:54215896-54216007	XLOC_007082
25	lnc-OPRK1-3	chr8:54308012-54308316	NONHSAT126588
26	lnc-OPRK1-4	chr8:54163578-54163645	NONHSAT126581
27	lnc-OPRK1-3	chr8:54307771-54308316	ENSG00000253369
28	lnc-OPRK1-3	chr8:54308012-54308316	NONHSAT126589
29	lnc-OPRK1-3	chr8:54308459-54308626	NONHSAT126588
30	lnc-OPRK1-4	chr8:54164009-54164257	NONHSAT126581
31	lnc-NPBWR1-1	chr8:54128859-54128983	ENSG00000254687.1

No data

Variant related genes	Relation type
ENSG00000265835	TF binding region
ENSG00000254687	TF binding region
ENSG00000260484	TF binding region
OPRK1	TF binding region
ENSG00000251871	TF binding region
ENSG00000248911	TF binding region
ENSG00000250494	TF binding region
ENSG00000253369	TF binding region
ENSG00000265835	CpG island
ENSG00000254687	CpG island
ENSG00000260484	CpG island
OPRK1	CpG island
ENSG00000251871	CpG island
ENSG00000248911	CpG island
ENSG00000250494	CpG island
ENSG00000253369	CpG island
ENSG00000082556	chromatin interactions

Extended variants
information (count: 10233 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:10233 , 50 per page) page: 1 2 3 4 5 6 7 ... 205

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs207469176	chr8:53873443-53873444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs556337700	chr8:53873474-53873475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs535033180	chr8:53873550-53873551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs551447818	chr8:53873567-53873568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs139389906	chr8:53873603-53873604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs66467113	chr8:53873613-53873614	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs150065874	chr8:53873614-53873615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs2360236	chr8:53873734-53873735	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs545629620	chr8:53873737-53873738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs182207635	chr8:53873795-53873796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs531350386	chr8:53873810-53873811	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs193122816	chr8:53873816-53873817	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs549848807	chr8:53873834-53873835	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs2262917	chr8:53873837-53873838	Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs149186477	chr8:53873868-53873869	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs187239386	chr8:53873879-53873880	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs2262916	chr8:53873894-53873895	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs370941331	chr8:53873905-53873906	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs555063303	chr8:53873925-53873926	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs552850563	chr8:53873932-53873933	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs571773999	chr8:53873940-53873941	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs190818063	chr8:53873941-53873942	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs556635891	chr8:53873960-53873961	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs574811299	chr8:53873969-53873970	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs535873529	chr8:53873975-53873976	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs553867294	chr8:53873989-53873990	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs373129588	chr8:53873990-53873991	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs180680868	chr8:53874011-53874012	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs563990321	chr8:53874022-53874023	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs575839591	chr8:53874053-53874054	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs543217105	chr8:53874054-53874055	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs561841114	chr8:53874056-53874057	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs528959541	chr8:53874112-53874113	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs147586765	chr8:53874113-53874114	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs142116760	chr8:53874148-53874149	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs532910156	chr8:53874164-53874165	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs552915630	chr8:53874178-53874179	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs185660602	chr8:53874179-53874180	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs538457823	chr8:53874183-53874184	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs557408926	chr8:53874208-53874209	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs550087230	chr8:53874228-53874229	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs557421108	chr8:53874271-53874272	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs7822512	chr8:53874273-53874274	Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs535570963	chr8:53874289-53874290	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs553794161	chr8:53874290-53874291	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs371209573	chr8:53874323-53874324	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs112292300	chr8:53874331-53874332	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs572108462	chr8:53874348-53874349	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs543796124	chr8:53874358-53874359	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs190070997	chr8:53874390-53874391	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
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
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Salivary gland tumor	18059337	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
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	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
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
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	22286061	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Sezary syndrome	18413736	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Uveal melanoma	20484589	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD
Colorectal cancer	21645411	CNVD

Chromatin state (count:885 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:53873000-53874600	Weak transcription	Dnd41	blood
2	chr8:53873800-53874400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr8:53874600-53876800	Enhancers	Dnd41	blood
4	chr8:53876800-53877800	Weak transcription	Dnd41	blood
5	chr8:53877800-53878800	Enhancers	Dnd41	blood
6	chr8:53878000-53878400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr8:53878200-53878600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
8	chr8:53878800-53882400	Weak transcription	Dnd41	blood
9	chr8:53881400-53881600	Enhancers	Thymus	Thymus
10	chr8:53881600-53883400	Weak transcription	Thymus	Thymus
11	chr8:53882200-53883000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr8:53882400-53882600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
13	chr8:53882400-53884800	Enhancers	Dnd41	blood
14	chr8:53882600-53887200	Enhancers	Fetal Intestine Small	intestine
15	chr8:53882800-53884800	Enhancers	Fetal Thymus	thymus
16	chr8:53882800-53887600	Enhancers	Fetal Intestine Large	intestine
17	chr8:53883000-53883400	Weak transcription	H1 Cell Line	embryonic stem cell
18	chr8:53883000-53884200	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr8:53883200-53883800	Enhancers	Duodenum Mucosa	Duodenum
20	chr8:53883200-53884600	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr8:53883200-53885000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr8:53883200-53885200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr8:53883200-53885200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr8:53883400-53883600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr8:53883400-53883800	Enhancers	Rectal Mucosa Donor 31	rectum
26	chr8:53883400-53884000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr8:53883400-53884000	Enhancers	Thymus	Thymus
28	chr8:53883400-53884400	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr8:53883400-53884600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr8:53883400-53884600	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr8:53883400-53885000	Enhancers	Primary B cells from peripheral blood	blood
32	chr8:53883400-53885200	Enhancers	H1 Cell Line	embryonic stem cell
33	chr8:53883400-53885400	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr8:53883400-53885400	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr8:53883400-53885400	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr8:53883600-53883800	Enhancers	Rectal Mucosa Donor 29	rectum
37	chr8:53883600-53883800	Enhancers	Stomach Mucosa	stomach
38	chr8:53883600-53883800	Enhancers	HepG2	liver
39	chr8:53883600-53884000	Enhancers	Small Intestine	intestine
40	chr8:53883600-53884200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr8:53883600-53884200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr8:53883600-53884600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr8:53883600-53884800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr8:53883600-53885400	Enhancers	H9 Cell Line	embryonic stem cell
45	chr8:53883800-53885000	Enhancers	Primary B cells from cord blood	blood
46	chr8:53883800-53886200	Weak transcription	Rectal Mucosa Donor 29	rectum
47	chr8:53883800-53886200	Weak transcription	Rectal Mucosa Donor 31	rectum
48	chr8:53883800-53886200	Weak transcription	Stomach Mucosa	stomach
49	chr8:53883800-53886200	Weak transcription	HepG2	liver
50	chr8:53884200-53884600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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