Variant report

Variant	nsv541769
Chromosome Location	chr13:49045566-49242357
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2753)
CpG islands
(count:1587)
Chromatin interactive
region (count:89)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:20)

(count:2753 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:49074874-49075254	HepG2	liver:	n/a	n/a
2	ARID3A	chr13:49154483-49154514	K562	blood:	n/a	n/a
3	ARID3A	chr13:49133929-49134176	K562	blood:	n/a	n/a
4	ARID3A	chr13:49106636-49107167	HepG2	liver:	n/a	n/a
5	ARID3A	chr13:49199275-49199453	HepG2	liver:	n/a	n/a
6	ARID3A	chr13:49163757-49164122	HepG2	liver:	n/a	n/a
7	ARID3A	chr13:49157738-49158332	HepG2	liver:	n/a	n/a
8	ARID3A	chr13:49169866-49170081	K562	blood:	n/a	n/a
9	ARID3A	chr13:49121950-49122070	HepG2	liver:	n/a	n/a
10	ARID3A	chr13:49200237-49200492	K562	blood:	n/a	n/a
11	ARID3A	chr13:49169770-49170119	HepG2	liver:	n/a	n/a
12	ARID3A	chr13:49200228-49200591	HepG2	liver:	n/a	n/a
13	ARID3A	chr13:49154380-49154733	HepG2	liver:	n/a	n/a
14	ARID3A	chr13:49089107-49089177	HepG2	liver:	n/a	n/a
15	ARID3A	chr13:49165779-49166168	HepG2	liver:	n/a	n/a
16	ARID3A	chr13:49203356-49203600	HepG2	liver:	n/a	n/a
17	ARID3A	chr13:49102183-49102295	HepG2	liver:	n/a	n/a
18	ARID3A	chr13:49137931-49138462	K562	blood:	n/a	n/a
19	ARID3A	chr13:49119999-49120054	HepG2	liver:	n/a	n/a
20	ATF1	chr13:49066725-49067036	K562	blood:	n/a	n/a
21	ATF1	chr13:49200172-49200564	K562	blood:	n/a	n/a
22	ATF2	chr13:49079683-49080292	GM12878	blood:	n/a	n/a
23	ATF2	chr13:49066194-49067099	GM12878	blood:	n/a	n/a
24	ATF2	chr13:49234449-49234951	GM12878	blood:	n/a	n/a
25	ATF2	chr13:49136260-49136920	GM12878	blood:	n/a	n/a
26	ATF2	chr13:49062979-49063610	GM12878	blood:	n/a	n/a
27	ATF2	chr13:49153159-49153854	GM12878	blood:	n/a	n/a
28	ATF2	chr13:49063069-49063536	GM12878	blood:	n/a	n/a
29	ATF2	chr13:49104780-49105437	GM12878	blood:	n/a	n/a
30	ATF2	chr13:49152608-49153895	GM12878	blood:	n/a	n/a
31	ATF2	chr13:49066426-49067129	GM12878	blood:	n/a	n/a
32	ATF2	chr13:49102790-49103305	GM12878	blood:	n/a	n/a
33	ATF2	chr13:49079723-49080279	GM12878	blood:	n/a	n/a
34	ATF2	chr13:49106745-49107353	GM12878	blood:	n/a	n/a
35	ATF2	chr13:49136294-49137061	GM12878	blood:	n/a	n/a
36	ATF3	chr13:49200207-49200533	K562	blood:	n/a	n/a
37	ATF3	chr13:49138155-49138461	K562	blood:	n/a	n/a
38	BACH1	chr13:49106959-49107550	H1-hESC	embryonic stem cell:	n/a	n/a
39	BACH1	chr13:49079289-49079578	H1-hESC	embryonic stem cell:	n/a	n/a
40	BATF	chr13:49234520-49234910	GM12878	blood:	n/a	chr13:49234568-49234578
41	BATF	chr13:49153243-49153666	GM12878	blood:	n/a	n/a
42	BATF	chr13:49079627-49080152	GM12878	blood:	n/a	n/a
43	BATF	chr13:49051371-49051600	GM12878	blood:	n/a	chr13:49051533-49051544
44	BATF	chr13:49145822-49146009	GM12878	blood:	n/a	n/a
45	BATF	chr13:49168239-49168462	GM12878	blood:	n/a	chr13:49168382-49168393
46	BATF	chr13:49136430-49136783	GM12878	blood:	n/a	n/a
47	BATF	chr13:49153307-49153679	GM12878	blood:	n/a	n/a
48	BATF	chr13:49051391-49051611	GM12878	blood:	n/a	chr13:49051533-49051544
49	BATF	chr13:49136432-49136799	GM12878	blood:	n/a	n/a
50	BATF	chr13:49234507-49234899	GM12878	blood:	n/a	chr13:49234568-49234578

(count:1587 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:49117085-49117135	BJ	skin:	n/a
2	chr13:49117085-49117135	BJ	skin:	n/a
3	chr13:49066969-49067019	PANC-1	pancreas:	n/a
4	chr13:49075016-49075066	Jurkat	blood:	n/a
5	chr13:49106778-49106828	Hepatocyte	liver:	n/a
6	chr13:49108353-49108403	SK-N-MC	brain:	n/a
7	chr13:49066969-49067019	HPAEpiC	pulmonary alveolar:	n/a
8	chr13:49076914-49076964	HRCEpiC	kidney:	n/a
9	chr13:49105050-49105100	HCM	heart:	n/a
10	chr13:49200201-49200251	K562	blood:	n/a
11	chr13:49105050-49105100	HAEpiC	amniotic membrane:	n/a
12	chr13:49175326-49175376	HCT-116	colon:	n/a
13	chr13:49108131-49108181	HL-60	blood:	n/a
14	chr13:49106753-49106803	SK-N-SH_RA	brain:	n/a
15	chr13:49107693-49107743	HIPEpiC	eye:	n/a
16	chr13:49106778-49106828	GM12878	blood:	n/a
17	chr13:49159767-49159817	NT2-D1	testis:	n/a
18	chr13:49106753-49106803	NT2-D1	testis:	n/a
19	chr13:49168127-49168177	HRPEpiC	eye:	n/a
20	chr13:49070825-49070875	AG09309	skin:	n/a
21	chr13:49105050-49105100	NHDF-neo	bronchial:	n/a
22	chr13:49107423-49107473	Hepatocyte	liver:	n/a
23	chr13:49175326-49175376	HIPEpiC	eye:	n/a
24	chr13:49108131-49108181	AG04449	skin:	fetal
25	chr13:49117085-49117135	H1-hESC	embryonic stem cell:	embryo
26	chr13:49107693-49107743	LNCaP	prostate:	n/a
27	chr13:49107423-49107473	PFSK-1	brain:	n/a
28	chr13:49070825-49070875	HAEpiC	amniotic membrane:	n/a
29	chr13:49159767-49159817	IMR90	lung:	fetal
30	chr13:49104302-49104352	HPAEpiC	pulmonary alveolar:	n/a
31	chr13:49107249-49107299	HRCEpiC	kidney:	n/a
32	chr13:49107249-49107299	SK-N-SH_RA	brain:	n/a
33	chr13:49070825-49070875	HepG2	liver:	n/a
34	chr13:49106778-49106828	SK-N-SH_RA	brain:	n/a
35	chr13:49107436-49107486	GM12891	blood:	n/a
36	chr13:49159767-49159817	HCPEpiC	choroid plexus:	n/a
37	chr13:49107249-49107299	NB4	blood:	n/a
38	chr13:49066969-49067019	PFSK-1	brain:	n/a
39	chr13:49070825-49070875	NH-A	brain:	n/a
40	chr13:49066868-49066918	NHBE	bronchial:	n/a
41	chr13:49226663-49226713	NH-A	brain:	n/a
42	chr13:49107116-49107166	IMR90	lung:	fetal
43	chr13:49107423-49107473	AG10803	skin:	n/a
44	chr13:49159767-49159817	HCT-116	colon:	n/a
45	chr13:49145436-49145486	SAEC	small airway:	n/a
46	chr13:49108131-49108181	ProgFib	skin:	n/a
47	chr13:49227121-49227171	NT2-D1	testis:	n/a
48	chr13:49107693-49107743	Caco-2	colon:	n/a
49	chr13:49200201-49200251	SK-N-MC	brain:	n/a
50	chr13:49200201-49200251	RPTEC	kidney:	n/a

(count:89 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr13:49057919..49060518-chr13:49066120..49068824,2	K562	blood:
2	chr13:49221601..49222385-chr13:49305871..49306516,2	MCF-7	breast:
3	chr13:49097151..49098767-chr13:49101729..49104209,2	K562	blood:
4	chr13:49081743..49084542-chr13:49085954..49089235,3	K562	blood:
5	chr13:49143466..49145650-chr13:49355908..49357695,2	MCF-7	breast:
6	chr13:49213689..49215557-chr13:49216870..49218702,2	K562	blood:
7	chr13:49107002..49107509-chr13:107220001..107220517,2	Hela-S3	cervix:
8	chr13:49105312..49106900-chr13:49113736..49116224,2	MCF-7	breast:
9	chr13:49090774..49093179-chr13:49096004..49098974,2	K562	blood:
10	chr13:49092461..49094974-chr13:49098743..49100899,2	K562	blood:
11	chr13:49115025..49117372-chr13:49140241..49143183,2	MCF-7	breast:
12	chr13:49106158..49108541-chr13:49108790..49110495,3	MCF-7	breast:
13	chr13:49106736..49108351-chr13:49112115..49113994,3	K562	blood:
14	chr13:49106818..49107420-chr2:172967559..172968104,2	HCT-116	colon:
15	chr13:49066305..49068745-chr13:49072101..49074756,2	MCF-7	breast:
16	chr13:49115025..49117372-chr13:49140241..49143183,2	MCF-7	breast:
17	chr13:49094520..49096357-chr13:49101326..49103599,2	MCF-7	breast:
18	chr13:49109125..49111040-chr13:49114592..49116444,2	K562	blood:
19	chr13:49109125..49111040-chr13:49114592..49116444,2	K562	blood:
20	chr13:49073253..49075349-chr13:49104032..49107682,5	MCF-7	breast:
21	chr13:49106089..49108573-chr13:49138293..49140212,2	MCF-7	breast:
22	chr13:49116019..49118411-chr13:49119146..49122086,2	K562	blood:
23	chr13:49088221..49089957-chr13:49104157..49106836,2	MCF-7	breast:
24	chr13:49075530..49077233-chr13:49077933..49080570,2	MCF-7	breast:
25	chr13:49217399..49217979-chr13:49342910..49343628,2	MCF-7	breast:
26	chr13:49141688..49143234-chr13:49148647..49150198,2	MCF-7	breast:
27	chr13:49075530..49077233-chr13:49077933..49080570,2	MCF-7	breast:
28	chr13:49145648..49148059-chr13:49151703..49153220,2	K562	blood:
29	chr13:49096194..49098388-chr13:49103789..49106979,3	MCF-7	breast:
30	chr13:48806307..48808548-chr13:49152200..49154470,2	MCF-7	breast:
31	chr13:49070136..49072576-chr13:49104860..49107906,3	MCF-7	breast:
32	chr13:49093025..49094796-chr13:49104131..49108138,4	MCF-7	breast:
33	chr13:49113319..49115711-chr13:49122578..49124381,2	K562	blood:
34	chr13:49063272..49066257-chr13:49067561..49069081,2	K562	blood:
35	chr13:49065216..49067091-chr13:49070291..49073195,2	K562	blood:
36	chr13:49106639..49107516-chr14:60714929..60715777,2	Hela-S3	cervix:
37	chr13:31191032..31191832-chr13:49106658..49107318,2	HCT-116	colon:
38	chr13:49090774..49093911-chr13:49094520..49097762,3	K562	blood:
39	chr13:49169295..49170510-chr13:49305795..49306796,15	MCF-7	breast:
40	chr13:49090774..49093911-chr13:49094520..49097762,3	K562	blood:
41	chr13:49068490..49070652-chr13:49071490..49073250,2	K562	blood:
42	chr13:49113085..49114630-chr13:49116071..49118855,2	MCF-7	breast:
43	chr1:121484521..121485222-chr13:49045277..49046048,2	MCF-7	breast:
44	chr13:49169593..49170465-chr13:49305139..49306545,8	MCF-7	breast:
45	chr13:49169501..49170445-chr13:49342944..49343864,14	MCF-7	breast:
46	chr13:49107018..49108572-chr13:49108963..49111065,3	MCF-7	breast:
47	chr13:49169482..49170418-chr13:49342940..49343870,6	K562	blood:
48	chr13:49109335..49111228-chr13:49113801..49116613,2	MCF-7	breast:
49	chr13:49240366..49242001-chr13:49295231..49296935,2	MCF-7	breast:
50	chr13:49106673..49108535-chr13:49114144..49118573,5	MCF-7	breast:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RB1-2	chr13:49106976-49107897	NONHSAT033718
2	lnc-RCBTB2-3	chr13:49151110-49151995	NONHSAT033722
3	lnc-RCBTB2-1	chr13:49142298-49142483	XLOC_010605
4	lnc-RCBTB2-2	chr13:49147244-49147453	XLOC_010606
5	lnc-RCBTB2-4	chr13:49108643-49109255	l_837_chr13:49108642-49112591_adrenal
6	lnc-RCBTB2-3	chr13:49152149-49152224	NONHSAT033722
7	lnc-RCBTB2-2	chr13:49144775-49144977	XLOC_010606
8	lnc-RCBTB2-4	chr13:49112005-49112263	l_837_chr13:49108642-49112591_adrenal
9	lnc-RCBTB2-1	chr13:49144444-49144479	XLOC_010605
10	lnc-RCBTB2-3	chr13:49154977-49155037	NONHSAT033722
11	lnc-RCBTB2-4	chr13:49112265-49112591	l_837_chr13:49108642-49112591_adrenal
12	lnc-RCBTB2-1	chr13:49143977-49144083	XLOC_010605

No data

(count:20 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	RB1	hsa-miR-192-5p	chr13:49055776-49055796
2	RB1	hsa-miR-93-5p	chr13:49055090-49055096
3	RB1	hsa-miR-132-3p	chr13:49055153-49055160
4	RB1	hsa-miR-215-5p	chr13:49055776-49055796
5	RB1	hsa-miR-106b-5p	chr13:49055077-49055097
6	RB1	hsa-miR-17-5p	chr13:49055090-49055096
7	RB1	hsa-miR-106a-5p	chr13:49055075-49055097
8	RB1	hsa-miR-26a-5p	chr13:49055007-49055029
9	RB1	hsa-miR-17-5p	chr13:49055075-49055097
10	RB1	hsa-miR-26a-5p	chr13:49055022-49055029
11	RB1	hsa-miR-93-5p	chr13:49055075-49055097
12	RB1	hsa-miR-20a-5p	chr13:49055075-49055097
13	RCBTB2	hsa-miR-26b-5p	chr13:49063578-49063597
14	RB1	hsa-miR-20a-5p	chr13:49055090-49055096
15	RB1	hsa-miR-106b-5p	chr13:49055090-49055096
16	RB1	hsa-miR-212-3p	chr13:49055153-49055160
17	RB1	hsa-miR-212-3p	chr13:49055140-49055160
18	RB1	hsa-miR-106a-5p	chr13:49055090-49055096
19	RB1	hsa-miR-132-3p	chr13:49055139-49055160
20	RB1	hsa-miR-335-5p	chr13:49054566-49054588

Variant related genes	Relation type
LINC01077	TF binding region
RCBTB2	TF binding region
RB1	TF binding region
LINC00462	TF binding region
LINC01077	CpG island
RCBTB2	CpG island
RB1	CpG island
LINC00462	CpG island
ENSG00000233610	chromatin interactions
ENSG00000233456	chromatin interactions
ENSG00000236651	chromatin interactions
ENSG00000254718	chromatin interactions
ENSG00000115844	chromatin interactions
ENSG00000136161	chromatin interactions
ENSG00000189403	chromatin interactions
ENSG00000132952	chromatin interactions
ENSG00000134884	chromatin interactions
ENSG00000136156	chromatin interactions
ENSG00000139687	chromatin interactions
ENSG00000106346	chromatin interactions
RNF145	miRNA target sites
RNF182	miRNA target sites

Extended variants
information (count: 6864 )
Associated
traits (count: 135 )

Variant overlapped rSNPs/rCNVs (count:6864 , 50 per page) page: 1 2 3 4 5 6 7 ... 138

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538653496	chr13:49045655-49045656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs71072103	chr13:49045709-49045710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs202110782	chr13:49045710-49045711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs78767790	chr13:49045713-49045714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs200265447	chr13:49045724-49045725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs192766762	chr13:49045735-49045736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs371792123	chr13:49045810-49045811	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs542837150	chr13:49045952-49045953	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs561092656	chr13:49046025-49046026	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs183939957	chr13:49046026-49046027	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs566710038	chr13:49046068-49046069	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs574062438	chr13:49046110-49046111	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs186893878	chr13:49046139-49046140	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs150635376	chr13:49046167-49046168	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs55926808	chr13:49046173-49046174	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs551368973	chr13:49046194-49046195	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs139747567	chr13:49046239-49046240	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs191282791	chr13:49046286-49046287	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs555040209	chr13:49046304-49046305	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs75052176	chr13:49046327-49046328	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs567555454	chr13:49046354-49046355	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs538449868	chr13:49046364-49046365	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs543846923	chr13:49046375-49046376	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs549585923	chr13:49046471-49046472	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs571324464	chr13:49046532-49046533	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs142214394	chr13:49046568-49046569	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs183481232	chr13:49046578-49046579	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs564132284	chr13:49046628-49046629	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs533413878	chr13:49046641-49046642	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs112758947	chr13:49046648-49046649	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs555867360	chr13:49046652-49046653	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs190539740	chr13:49046665-49046666	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs572346522	chr13:49046678-49046679	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs536581639	chr13:49046688-49046689	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs369151585	chr13:49046693-49046694	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs560808419	chr13:49046707-49046708	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs182383143	chr13:49046708-49046709	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs554916475	chr13:49046720-49046721	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs576126456	chr13:49046728-49046729	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs543606149	chr13:49046803-49046804	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs4151607	chr13:49046857-49046858	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs529510038	chr13:49046922-49046923	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs578078295	chr13:49046926-49046927	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs544998259	chr13:49046967-49046968	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs185274998	chr13:49047029-49047030	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs527964405	chr13:49047040-49047041	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs549629439	chr13:49047098-49047099	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs549232506	chr13:49047235-49047236	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs190178026	chr13:49047312-49047313	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs561649584	chr13:49047320-49047321	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:135)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Squamous cell cancer	20885788	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Thyroid cancer	19087340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	17899364	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	16774939	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Trisomy	24170809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Alveolar rhabdomyosarcoma	16790082	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	19242612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	17245344	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Retinoblastoma	21504564	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Mental retardation	17502991	CNVD
Retinoblastoma	17502991	CNVD
Bipolar disorder	18458673	CNVD
Liposarcoma	21253554	CNVD
T-cell lymphomas	19863542	CNVD
Cervical cancer	21062161	CNVD
microdeletion syndrome	19284877	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Multiple myeloma	19135901	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Prostate cancer	16461572	CNVD
Merkel cell carcinoma	19020549	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	19435819	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Breast cancer	21858162	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	17237825	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Lung adenocarcinoma	21151896	CNVD
Breast cancer	21518781	CNVD
Mantle cell lymphoma	21518781	CNVD
Ovarian cancer	21518781	CNVD
Retinoblastoma	21518781	CNVD
Myelofibrosis	22110671	CNVD
Hereditary prostate cancer	22028916	CNVD
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Prostate cancer	17217626	CNVD
Ovarian cancer	21781307	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
Chronic myeloid leukemia	21384125	CNVD
Attention deficit hyperactivity disorder	22214315	CNVD
Chronic motor tic disorder	22214315	CNVD
Schizophrenia	22214315	CNVD
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD
Autism	22495309	CNVD
Osteosarcoma	21215367	CNVD
Sezary syndrome	18413736	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Lung adenocarcinoma	21935476	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:4429 , 50 per page) page: 1 2 3 4 5 6 7 ... 89

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:49017400-49062200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr13:49018000-49062400	Weak transcription	Fetal Brain Male	brain
3	chr13:49020800-49062000	Weak transcription	Fetal Kidney	kidney
4	chr13:49021200-49058600	Weak transcription	Hela-S3	cervix
5	chr13:49023800-49061000	Weak transcription	Small Intestine	intestine
6	chr13:49023800-49073800	Weak transcription	NH-A	brain
7	chr13:49024000-49059000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
8	chr13:49025600-49056800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
9	chr13:49025600-49066200	Weak transcription	Psoas Muscle	Psoas
10	chr13:49027600-49049200	Weak transcription	A549	lung
11	chr13:49028000-49071000	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr13:49029000-49046000	Weak transcription	HSMMtube	muscle
13	chr13:49029200-49062000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr13:49029400-49052400	Weak transcription	K562	blood
15	chr13:49030600-49070600	Weak transcription	H1 Cell Line	embryonic stem cell
16	chr13:49031600-49049600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
17	chr13:49031600-49055800	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr13:49031600-49066200	Weak transcription	Rectal Smooth Muscle	rectum
19	chr13:49031800-49045800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
20	chr13:49031800-49052000	Weak transcription	HepG2	liver
21	chr13:49031800-49052600	Weak transcription	Placenta	Placenta
22	chr13:49031800-49059200	Weak transcription	Primary T helper cells PMA-I stimulated	--
23	chr13:49031800-49060200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
24	chr13:49031800-49060600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
25	chr13:49031800-49065400	Weak transcription	Brain Substantia Nigra	brain
26	chr13:49032000-49050800	Weak transcription	Brain Hippocampus Middle	brain
27	chr13:49032000-49065600	Weak transcription	Brain Anterior Caudate	brain
28	chr13:49032000-49066200	Weak transcription	Colonic Mucosa	Colon
29	chr13:49032200-49053400	Weak transcription	Skeletal Muscle Male	skeletal muscle
30	chr13:49032200-49054000	Weak transcription	Aorta	Aorta
31	chr13:49032200-49056000	Weak transcription	Brain Germinal Matrix	brain
32	chr13:49032400-49049000	Weak transcription	Lung	lung
33	chr13:49032400-49052600	Weak transcription	NHLF	lung
34	chr13:49032400-49053000	Weak transcription	Sigmoid Colon	Sigmoid Colon
35	chr13:49032400-49062600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr13:49032400-49066200	Weak transcription	Spleen	Spleen
37	chr13:49032400-49066600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr13:49032400-49066600	Weak transcription	Ovary	ovary
39	chr13:49032400-49067400	Weak transcription	Pancreas	Pancrea
40	chr13:49032400-49067600	Weak transcription	Gastric	stomach
41	chr13:49032600-49051600	Weak transcription	HMEC	breast
42	chr13:49032600-49055000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr13:49032800-49066200	Weak transcription	Stomach Smooth Muscle	stomach
44	chr13:49034400-49073800	Weak transcription	Esophagus	oesophagus
45	chr13:49035200-49073400	Weak transcription	Fetal Intestine Small	intestine
46	chr13:49035400-49052800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
47	chr13:49035600-49052000	Weak transcription	Liver	Liver
48	chr13:49035600-49052800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr13:49035600-49053400	Weak transcription	Cortex derived primary cultured neurospheres	brain
50	chr13:49035600-49065400	Weak transcription	Brain Cingulate Gyrus	brain

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