Variant report

Variant	nsv541745
Chromosome Location	chr13:30621351-30741022
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2745)
CpG islands
(count:1342)
Chromatin interactive
region (count:120)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2745 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:30706687-30706943	HepG2	liver:	n/a	n/a
2	ARID3A	chr13:30688611-30688811	HepG2	liver:	n/a	n/a
3	ARID3A	chr13:30687027-30687469	HepG2	liver:	n/a	n/a
4	ARID3A	chr13:30689142-30689418	HepG2	liver:	n/a	n/a
5	ATF1	chr13:30623887-30624232	K562	blood:	n/a	n/a
6	ATF2	chr13:30716418-30716958	GM12878	blood:	n/a	n/a
7	ATF2	chr13:30733565-30734000	GM12878	blood:	n/a	n/a
8	ATF2	chr13:30706720-30707164	GM12878	blood:	n/a	n/a
9	ATF2	chr13:30687012-30687374	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr13:30706702-30707043	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr13:30715067-30715488	GM12878	blood:	n/a	n/a
12	ATF2	chr13:30689113-30689376	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr13:30719963-30720650	GM12878	blood:	n/a	n/a
14	ATF2	chr13:30687031-30687478	GM12878	blood:	n/a	n/a
15	ATF2	chr13:30733546-30734112	GM12878	blood:	n/a	n/a
16	ATF2	chr13:30687068-30687353	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr13:30731484-30732193	GM12878	blood:	n/a	n/a
18	ATF2	chr13:30719812-30721127	GM12878	blood:	n/a	n/a
19	ATF2	chr13:30716441-30717002	GM12878	blood:	n/a	n/a
20	ATF3	chr13:30718192-30718533	GM12878	blood:	n/a	n/a
21	ATF3	chr13:30718260-30718406	GM12878	blood:	n/a	n/a
22	ATF3	chr13:30718277-30718404	K562	blood:	n/a	n/a
23	ATF3	chr13:30689105-30689355	K562	blood:	n/a	n/a
24	BACH1	chr13:30689058-30689450	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr13:30679756-30679901	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr13:30626681-30626711	K562	blood:	n/a	n/a
27	BACH1	chr13:30689896-30689903	K562	blood:	n/a	n/a
28	BATF	chr13:30716370-30716820	GM12878	blood:	n/a	n/a
29	BATF	chr13:30689026-30689419	GM12878	blood:	n/a	chr13:30689204-30689214 chr13:30689203-30689214
30	BATF	chr13:30719898-30720629	GM12878	blood:	n/a	chr13:30720253-30720262
31	BATF	chr13:30715122-30715507	GM12878	blood:	n/a	n/a
32	BATF	chr13:30715602-30715845	GM12878	blood:	n/a	n/a
33	BATF	chr13:30720016-30720589	GM12878	blood:	n/a	chr13:30720253-30720262
34	BATF	chr13:30715139-30715414	GM12878	blood:	n/a	n/a
35	BATF	chr13:30694253-30694645	GM12878	blood:	n/a	n/a
36	BATF	chr13:30733545-30734005	GM12878	blood:	n/a	chr13:30733724-30733735
37	BCL11A	chr13:30720090-30720423	GM12878	blood:	n/a	chr13:30720267-30720276
38	BCL11A	chr13:30720023-30720600	GM12878	blood:	n/a	chr13:30720267-30720276
39	BCL11A	chr13:30715050-30715432	GM12878	blood:	n/a	n/a
40	BCL3	chr13:30733585-30734032	GM12878	blood:	n/a	n/a
41	BCL3	chr13:30731657-30732135	GM12878	blood:	n/a	n/a
42	BCL3	chr13:30720008-30720550	GM12878	blood:	n/a	chr13:30720267-30720276
43	BCLAF1	chr13:30706603-30707145	GM12878	blood:	n/a	n/a
44	BCLAF1	chr13:30719944-30720582	GM12878	blood:	n/a	chr13:30720267-30720276
45	BCLAF1	chr13:30687050-30687527	GM12878	blood:	n/a	n/a
46	BCLAF1	chr13:30688997-30689490	GM12878	blood:	n/a	chr13:30689338-30689347 chr13:30689053-30689066 chr13:30689303-30689316
47	BCLAF1	chr13:30719835-30720617	GM12878	blood:	n/a	chr13:30720267-30720276
48	BCLAF1	chr13:30731558-30732196	GM12878	blood:	n/a	n/a
49	BCLAF1	chr13:30720721-30721128	GM12878	blood:	n/a	n/a
50	BHLHE40	chr13:30623955-30624088	K562	blood:	n/a	n/a

(count:1342 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:30643156-30643206	SK-N-SH	brain:	n/a
2	chr13:30728534-30728584	HEEpiC	esophagus:	n/a
3	chr13:30686841-30686891	SAEC	small airway:	n/a
4	chr13:30728819-30728869	SK-N-SH	brain:	n/a
5	chr13:30728534-30728584	PrEC	prostate:	n/a
6	chr13:30692581-30692631	HCT-116	colon:	n/a
7	chr13:30700159-30700209	AG10803	skin:	n/a
8	chr13:30626440-30626490	U87	brain:	n/a
9	chr13:30692581-30692631	HCPEpiC	choroid plexus:	n/a
10	chr13:30707265-30707315	HUVEC	blood vessel:	n/a
11	chr13:30728236-30728286	HCM	heart:	n/a
12	chr13:30689528-30689578	IMR90	lung:	fetal
13	chr13:30728534-30728584	T-47D	breast:	n/a
14	chr13:30692581-30692631	HCM	heart:	n/a
15	chr13:30689274-30689324	MCF10A-Er-Src	breast:	n/a
16	chr13:30688502-30688552	SK-N-SH	brain:	n/a
17	chr13:30728812-30728862	HUVEC	blood vessel:	n/a
18	chr13:30692581-30692631	NB4	blood:	n/a
19	chr13:30728819-30728869	T-47D	breast:	n/a
20	chr13:30700159-30700209	Hepatocyte	liver:	n/a
21	chr13:30688865-30688915	HAEpiC	amniotic membrane:	n/a
22	chr13:30717380-30717430	Jurkat	blood:	n/a
23	chr13:30707265-30707315	HEEpiC	esophagus:	n/a
24	chr13:30707265-30707315	SKMC	muscle:	n/a
25	chr13:30707119-30707169	GM12892	blood:	n/a
26	chr13:30688865-30688915	HUVEC	blood vessel:	n/a
27	chr13:30728236-30728286	HL-60	blood:	n/a
28	chr13:30707119-30707169	HRPEpiC	eye:	n/a
29	chr13:30689528-30689578	CMK	blood:	n/a
30	chr13:30728099-30728149	GM12891	blood:	n/a
31	chr13:30727927-30727977	AG10803	skin:	n/a
32	chr13:30643156-30643206	PrEC	prostate:	n/a
33	chr13:30728099-30728149	H1-hESC	embryonic stem cell:	embryo
34	chr13:30688865-30688915	HRCEpiC	kidney:	n/a
35	chr13:30707585-30707635	H1-hESC	embryonic stem cell:	embryo
36	chr13:30689009-30689059	BJ	skin:	n/a
37	chr13:30688502-30688552	PFSK-1	brain:	n/a
38	chr13:30643156-30643206	MCF10A-Er-Src	breast:	n/a
39	chr13:30728819-30728869	Hepatocyte	liver:	n/a
40	chr13:30688865-30688915	NHBE	bronchial:	n/a
41	chr13:30688502-30688552	T-47D	breast:	n/a
42	chr13:30689274-30689324	MCF-7	breast:	n/a
43	chr13:30689009-30689059	HCPEpiC	choroid plexus:	n/a
44	chr13:30688502-30688552	HCPEpiC	choroid plexus:	n/a
45	chr13:30728819-30728869	HRE	kidney:	n/a
46	chr13:30626440-30626490	AG04450	lung:	fetal
47	chr13:30689528-30689578	Jurkat	blood:	n/a
48	chr13:30688865-30688915	HRE	kidney:	n/a
49	chr13:30728812-30728862	Jurkat	blood:	n/a
50	chr13:30740197-30740247	AG09309	skin:	n/a

(count:120 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr13:30688932..30689485-chr13:30732660..30733617,2	MCF-7	breast:
2	chr13:30689194..30691299-chr13:30696452..30698373,2	K562	blood:
3	chr13:30702300..30704333-chr13:30714151..30716262,2	K562	blood:
4	chr13:30710616..30714136-chr13:30716937..30719066,3	K562	blood:
5	chr13:30707361..30710289-chr13:30714464..30717739,4	MCF-7	breast:
6	chr13:30675175..30677266-chr13:30681327..30683065,2	MCF-7	breast:
7	chr13:30347146..30349526-chr13:30687739..30689607,2	MCF-7	breast:
8	chr13:30697642..30699768-chr13:30715433..30718388,2	MCF-7	breast:
9	chr13:30716922..30719833-chr13:30752505..30754476,2	MCF-7	breast:
10	chr13:30669291..30671115-chr13:30673026..30674764,2	K562	blood:
11	chr13:30687723..30690408-chr13:30699734..30701487,2	MCF-7	breast:
12	chr13:30706815..30707417-chr13:30908978..30909886,3	MCF-7	breast:
13	chr13:30418877..30421858-chr13:30687750..30689569,3	MCF-7	breast:
14	chr13:30403000..30404793-chr13:30686519..30690620,3	MCF-7	breast:
15	chr13:30738155..30739907-chr13:30743836..30746673,2	K562	blood:
16	chr13:30268179..30269731-chr13:30686906..30689381,2	MCF-7	breast:
17	chr13:30651986..30653783-chr13:30687863..30690496,2	MCF-7	breast:
18	chr13:30686343..30690173-chr13:31036596..31040141,3	MCF-7	breast:
19	chr13:30672310..30673982-chr13:30681017..30682705,2	MCF-7	breast:
20	chr13:30344222..30347052-chr13:30686907..30688799,2	MCF-7	breast:
21	chr13:30738759..30741658-chr13:30748183..30751175,2	MCF-7	breast:
22	chr13:30702300..30704333-chr13:30714151..30716262,2	K562	blood:
23	chr13:30624543..30627399-chr13:30640626..30642566,2	MCF-7	breast:
24	chr13:30625738..30627746-chr13:30629378..30631883,2	K562	blood:
25	chr13:30689181..30689782-chr13:30706409..30706933,2	MCF-7	breast:
26	chr13:30420849..30425995-chr13:30676959..30681993,8	MCF-7	breast:
27	chr13:30422658..30425963-chr13:30681369..30690318,16	MCF-7	breast:
28	chr13:30644483..30648351-chr13:30648983..30651482,3	MCF-7	breast:
29	chr13:30707361..30710289-chr13:30714464..30717739,4	MCF-7	breast:
30	chr13:30683338..30685506-chr13:30693014..30696213,3	MCF-7	breast:
31	chr13:30669991..30672596-chr13:30676116..30677824,2	K562	blood:
32	chr13:30497791..30500360-chr13:30674614..30679278,4	MCF-7	breast:
33	chr13:30690726..30692990-chr13:30715205..30717386,2	MCF-7	breast:
34	chr13:30654713..30656574-chr13:30657966..30660630,2	MCF-7	breast:
35	chr13:30678307..30680282-chr13:30680311..30683353,3	MCF-7	breast:
36	chr13:30668684..30670945-chr13:30671996..30673872,2	MCF-7	breast:
37	chr13:30081296..30083385-chr13:30689063..30690673,2	MCF-7	breast:
38	chr13:30654713..30656574-chr13:30657966..30660630,2	MCF-7	breast:
39	chr13:30498435..30501654-chr13:30681390..30683059,3	MCF-7	breast:
40	chr13:30720797..30722317-chr8:43092931..43095226,2	K562	blood:
41	chr13:30625738..30627746-chr13:30629378..30631883,2	K562	blood:
42	chr13:30721961..30724488-chr13:30755473..30758076,2	K562	blood:
43	chr13:30413488..30415848-chr13:30648656..30650250,2	MCF-7	breast:
44	chr13:30669291..30671115-chr13:30673026..30674764,2	K562	blood:
45	chr13:30688932..30689485-chr13:30732660..30733617,2	MCF-7	breast:
46	chr13:30428025..30429694-chr13:30678131..30680378,2	MCF-7	breast:
47	chr13:30720797..30723795-chr8:43093825..43096195,3	MCF-7	breast:
48	chr13:30687972..30690132-chr13:31190210..31193033,2	MCF-7	breast:
49	chr13:30621873..30623731-chr13:30625663..30627345,2	MCF-7	breast:
50	chr13:30415961..30419397-chr13:30686617..30690558,4	MCF-7	breast:

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KATNAL1-2	chr13:30726023-30726286	XLOC_010554
2	lnc-RP11-90M5.1.1-5	chr13:30677318-30678167	NONHSAT032762
3	lnc-KATNAL1-4	chr13:30682906-30683005	XLOC_010553
4	lnc-RP11-90M5.1.1-5	chr13:30680912-30681279	NONHSAT032762
5	lnc-RP11-90M5.1.1-3	chr13:30728426-30729034	NONHSAT032767
6	lnc-KATNAL1-4	chr13:30682906-30683012	XLOC_010553
7	lnc-KATNAL1-4	chr13:30681736-30682108	XLOC_010553
8	lnc-KATNAL1-2	chr13:30727171-30733758	XLOC_010554
9	lnc-KATNAL1-4	chr13:30677366-30679832	XLOC_010553
10	lnc-KATNAL1-4	chr13:30677315-30679832	ENSG00000224511
11	lnc-RP11-90M5.1.1-5	chr13:30681295-30681333	NONHSAT032762
12	lnc-RP11-90M5.1.1-3	chr13:30728426-30728723	ENSG00000232643
13	lnc-RP11-90M5.1.1-5	chr13:30678175-30679036	NONHSAT032762
14	lnc-RP11-90M5.1.1-3	chr13:30728203-30728278	ENSG00000232643
15	lnc-KATNAL1-4	chr13:30682906-30683005	ENSG00000224511
16	lnc-RP11-90M5.1.1-3	chr13:30727850-30727977	NONHSAT032767

No data

Variant related genes	Relation type
LINC00385	TF binding region
LINC00384	TF binding region
LINC00365	TF binding region
LINC00385	CpG island
LINC00384	CpG island
LINC00365	CpG island
ENSG00000266505	chromatin interactions
ENSG00000232117	chromatin interactions
ENSG00000122042	chromatin interactions
ENSG00000132952	chromatin interactions
ENSG00000224405	chromatin interactions
ENSG00000232643	chromatin interactions
ENSG00000189403	chromatin interactions
ENSG00000102781	chromatin interactions
ENSG00000224511	chromatin interactions
ENSG00000122043	chromatin interactions
CREBZF	miRNA target sites
AK2	miRNA target sites
AIF1L	miRNA target sites

Extended variants
information (count: 4705 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:4705 , 50 per page) page: 1 2 3 4 5 6 7 ... 95

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565407987	chr13:30621359-30621360	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs527748138	chr13:30621382-30621383	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs570287757	chr13:30621395-30621396	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs567501767	chr13:30621439-30621440	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs536646101	chr13:30621492-30621493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs201883828	chr13:30621533-30621534	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs549702154	chr13:30621536-30621537	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs569596230	chr13:30621542-30621543	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs145760076	chr13:30621553-30621554	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs558299830	chr13:30621561-30621562	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs185721398	chr13:30621572-30621573	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs117649582	chr13:30621584-30621585	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs148955645	chr13:30621594-30621595	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs626014	chr13:30621646-30621647	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs543396582	chr13:30621685-30621686	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs35278262	chr13:30621707-30621708	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs142751752	chr13:30621731-30621732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs147671394	chr13:30621766-30621767	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs625142	chr13:30621842-30621843	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs191673157	chr13:30621847-30621848	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs1041579	chr13:30621851-30621852	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs541212475	chr13:30621876-30621877	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs561424398	chr13:30621881-30621882	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs80077787	chr13:30621899-30621900	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs549740710	chr13:30621925-30621926	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs183494402	chr13:30621926-30621927	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs1041578	chr13:30621969-30621970	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs551963920	chr13:30621976-30621977	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs17074270	chr13:30621995-30621996	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs146897485	chr13:30622066-30622067	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs541751029	chr13:30622085-30622086	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs554410607	chr13:30622087-30622088	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs139382856	chr13:30622093-30622094	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs111703076	chr13:30622123-30622124	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs537073588	chr13:30622175-30622176	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs141738510	chr13:30622182-30622183	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs576816383	chr13:30622214-30622215	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs545668921	chr13:30622232-30622233	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs559290458	chr13:30622267-30622268	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs572592756	chr13:30622306-30622307	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs34253652	chr13:30622325-30622326	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs556735458	chr13:30622337-30622338	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs541595035	chr13:30622340-30622341	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs34568322	chr13:30622351-30622352	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs188939618	chr13:30622415-30622416	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs530179775	chr13:30622439-30622440	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs543425983	chr13:30622445-30622446	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs563303574	chr13:30622509-30622510	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs11619450	chr13:30622539-30622540	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs561511268	chr13:30622547-30622548	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Cancer	20164920	CNVD
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
Lung cancer	18438408	CNVD
Burkitt''s lymphoma	18698080	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	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
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	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
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Squamous cell cancer	20885788	CNVD
Thyroid cancer	19087340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Malignant glioma	17146433	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
Acute lymphoblastic leukemia	21339820	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Myelofibrosis	22110671	CNVD
Non-small cell lung cancer	21829676	CNVD
Retinoblastoma	22278416	CNVD
Peters Plus syndrome	16909395	CNVD
Trisomy	24170809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Breast cancer	20031965	CNVD
Colorectal cancer	19287155	CNVD
Ovarian cancer	19047089	CNVD
Alveolar rhabdomyosarcoma	16790082	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
Prostate cancer	18632612	CNVD
Prostate cancer	21147910	CNVD
Melanoma	20877625	CNVD
Colorectal cancer	21645411	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Congenital anomalies of the kidney and urinary tract	17440070	CNVD
Cancer	17440070	CNVD

Chromatin state (count:2188 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:30612000-30625600	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr13:30614800-30625800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr13:30618400-30621400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr13:30618600-30621800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr13:30619200-30622000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr13:30619400-30625600	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr13:30619800-30621600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr13:30619800-30621600	Enhancers	NH-A	brain
9	chr13:30619800-30621800	Enhancers	NHDF-Ad	bronchial
10	chr13:30619800-30622200	Enhancers	HSMM	muscle
11	chr13:30619800-30622400	Enhancers	HSMMtube	muscle
12	chr13:30619800-30622400	Enhancers	Osteobl	bone
13	chr13:30620000-30622200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr13:30620000-30622200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr13:30620000-30622400	Enhancers	Cortex derived primary cultured neurospheres	brain
16	chr13:30620200-30626600	Weak transcription	Stomach Mucosa	stomach
17	chr13:30620600-30623600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr13:30620800-30621600	Weak transcription	Duodenum Mucosa	Duodenum
19	chr13:30620800-30622200	Enhancers	Muscle Satellite Cultured Cells	--
20	chr13:30620800-30623800	Weak transcription	NHEK	skin
21	chr13:30620800-30625800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr13:30621000-30622000	Enhancers	Liver	Liver
23	chr13:30621000-30622400	Enhancers	Primary T cells from cord blood	blood
24	chr13:30621000-30622400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr13:30621000-30623600	Weak transcription	Placenta Amnion	Placenta Amnion
26	chr13:30621200-30622000	Enhancers	Sigmoid Colon	Sigmoid Colon
27	chr13:30621200-30622200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr13:30621200-30622400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
29	chr13:30621200-30622400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
30	chr13:30621200-30622600	Enhancers	Primary hematopoietic stem cells short term culture	blood
31	chr13:30621200-30623800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr13:30621400-30622200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
33	chr13:30621400-30622200	Enhancers	Fetal Intestine Small	intestine
34	chr13:30621400-30622200	Enhancers	Dnd41	blood
35	chr13:30621400-30622400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr13:30621400-30622400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr13:30621600-30622000	Enhancers	Primary T helper cells PMA-I stimulated	--
38	chr13:30621600-30622000	Enhancers	Duodenum Mucosa	Duodenum
39	chr13:30621600-30622200	Enhancers	Primary T killer memory cells from peripheral blood	blood
40	chr13:30621600-30622400	Enhancers	Breast Myoepithelial Primary Cells	Breast
41	chr13:30621600-30622400	Enhancers	Primary T cells fromperipheralblood	blood
42	chr13:30621600-30622400	Enhancers	Primary T helper naive cells from peripheral blood	blood
43	chr13:30621600-30622400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
44	chr13:30621600-30622400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr13:30621600-30622400	Enhancers	Small Intestine	intestine
46	chr13:30621600-30624000	Weak transcription	NH-A	brain
47	chr13:30621800-30622200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
48	chr13:30621800-30622200	Enhancers	Primary T helper cells fromperipheralblood	blood
49	chr13:30621800-30622400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
50	chr13:30622000-30623000	Weak transcription	Duodenum Mucosa	Duodenum

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