Variant report

Variant	nsv530416
Chromosome Location	chr13:66198235-67126195
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3803)
CpG islands
(count:794)
Chromatin interactive
region (count:54)
LncRNA
region (count:24)
Mature miRNA
region (count: 3)
miRNA target
sites (count:3)

(count:3803 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:66886857-66887028	HepG2	liver:	n/a	n/a
2	ARID3A	chr13:67024589-67024601	K562	blood:	n/a	n/a
3	ARID3A	chr13:66643768-66644097	K562	blood:	n/a	n/a
4	ARID3A	chr13:66651230-66651680	K562	blood:	n/a	n/a
5	ARID3A	chr13:66713473-66713809	HepG2	liver:	n/a	n/a
6	ARID3A	chr13:66650602-66650906	K562	blood:	n/a	n/a
7	ARID3A	chr13:66648258-66648447	K562	blood:	n/a	n/a
8	ARID3A	chr13:66784968-66784973	HepG2	liver:	n/a	n/a
9	ATF1	chr13:66990708-66990955	K562	blood:	n/a	n/a
10	ATF1	chr13:66648256-66648525	K562	blood:	n/a	n/a
11	ATF1	chr13:66999986-67000196	K562	blood:	n/a	n/a
12	ATF1	chr13:66643737-66644023	K562	blood:	n/a	n/a
13	ATF1	chr13:66650593-66650896	K562	blood:	n/a	n/a
14	ATF2	chr13:66798630-66799137	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr13:66712423-66712799	GM12878	blood:	n/a	n/a
16	ATF3	chr13:66886740-66887227	A549	lung:	n/a	n/a
17	BACH1	chr13:67078100-67078397	H1-hESC	embryonic stem cell:	n/a	chr13:67078231-67078245
18	BATF	chr13:66712465-66712951	GM12878	blood:	n/a	n/a
19	BATF	chr13:67052441-67052616	GM12878	blood:	n/a	n/a
20	BATF	chr13:66712420-66712936	GM12878	blood:	n/a	n/a
21	BATF	chr13:66702801-66703238	GM12878	blood:	n/a	n/a
22	BATF	chr13:67081195-67081436	GM12878	blood:	n/a	n/a
23	BCL11A	chr13:66798709-66799125	H1-hESC	embryonic stem cell:	n/a	n/a
24	BCL11A	chr13:66712457-66712949	GM12878	blood:	n/a	chr13:66712844-66712853
25	BCL11A	chr13:66798756-66799093	H1-hESC	embryonic stem cell:	n/a	n/a
26	BCL11A	chr13:66702875-66703088	GM12878	blood:	n/a	n/a
27	BCL11A	chr13:66712423-66713013	GM12878	blood:	n/a	chr13:66712844-66712853
28	BCL11A	chr13:66702751-66703109	GM12878	blood:	n/a	n/a
29	BCL3	chr13:66886752-66887345	A549	lung:	n/a	n/a
30	BCL3	chr13:66886608-66887994	A549	lung:	n/a	n/a
31	BCLAF1	chr13:66712465-66712857	GM12878	blood:	n/a	chr13:66712844-66712853
32	BHLHE40	chr13:66712457-66712998	GM12878	blood:	n/a	n/a
33	BHLHE40	chr13:66902776-66902779	K562	blood:	n/a	n/a
34	BHLHE40	chr13:66739043-66739104	K562	blood:	n/a	n/a
35	BHLHE40	chr13:66212820-66213067	GM12878	blood:	n/a	n/a
36	BHLHE40	chr13:66917482-66917943	K562	blood:	n/a	n/a
37	BHLHE40	chr13:66648396-66648557	K562	blood:	n/a	n/a
38	BRCA1	chr13:66878245-66878246	Hela-S3	cervix:	n/a	n/a
39	BRCA1	chr13:67088395-67088424	H1-hESC	embryonic stem cell:	n/a	n/a
40	BRCA1	chr13:66712793-66712993	GM12878	blood:	n/a	n/a
41	CBX3	chr13:66643667-66644035	K562	blood:	n/a	n/a
42	CBX3	chr13:66861033-66861253	K562	blood:	n/a	n/a
43	CBX3	chr13:66784784-66785224	HCT-116	colon:	n/a	n/a
44	CBX3	chr13:66212653-66213113	HCT-116	colon:	n/a	n/a
45	CBX3	chr13:66784811-66785347	HCT-116	colon:	n/a	n/a
46	CCNT2	chr13:66589547-66589747	K562	blood:	n/a	n/a
47	CCNT2	chr13:66617039-66617239	K562	blood:	n/a	n/a
48	CEBPB	chr13:66977771-66978130	HepG2	liver:	n/a	chr13:66977939-66977950
49	CEBPB	chr13:66212723-66213083	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr13:67082251-67082727	A549	lung:	n/a	chr13:67082691-67082708 chr13:67082473-67082484 chr13:67082694-67082707

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:67101887-67101937	K562	blood:	n/a
2	chr13:67101887-67101937	K562	blood:	n/a
3	chr13:66583686-66583736	HAEpiC	amniotic membrane:	n/a
4	chr13:67101887-67101937	H1-hESC	embryonic stem cell:	embryo
5	chr13:66583583-66583633	BE2_C	brain:	n/a
6	chr13:66983730-66983780	SK-N-SH_RA	brain:	n/a
7	chr13:67101887-67101937	AoSMC	blood vessel:	n/a
8	chr13:66919912-66919962	HNPCEpiC	eye:	n/a
9	chr13:66981290-66981340	GM12892	blood:	n/a
10	chr13:66583583-66583633	BJ	skin:	n/a
11	chr13:66929165-66929215	ECC-1	luminal epithelium:	n/a
12	chr13:66919912-66919962	NB4	blood:	n/a
13	chr13:66501111-66501161	HRE	kidney:	n/a
14	chr13:66252177-66252227	AG09309	skin:	n/a
15	chr13:66583686-66583736	HCF	heart:	n/a
16	chr13:66501111-66501161	NT2-D1	testis:	n/a
17	chr13:66929165-66929215	AG04449	skin:	fetal
18	chr13:66919912-66919962	PrEC	prostate:	n/a
19	chr13:67101887-67101937	MCF-7	breast:	n/a
20	chr13:66983730-66983780	SAEC	small airway:	n/a
21	chr13:67101887-67101937	Caco-2	colon:	n/a
22	chr13:66322551-66322601	NHDF-neo	bronchial:	n/a
23	chr13:67101887-67101937	AG10803	skin:	n/a
24	chr13:66252177-66252227	Hepatocyte	liver:	n/a
25	chr13:66252177-66252227	RPTEC	kidney:	n/a
26	chr13:66981290-66981340	ovcar-3	ovarian:	n/a
27	chr13:66983730-66983780	HEK293	kidney:	embryo
28	chr13:66607275-66607325	HCF	heart:	n/a
29	chr13:66501111-66501161	HIPEpiC	eye:	n/a
30	chr13:66607275-66607325	GM19239	blood:	n/a
31	chr13:66981290-66981340	HRCEpiC	kidney:	n/a
32	chr13:66252177-66252227	PFSK-1	brain:	n/a
33	chr13:66919912-66919962	AG04450	lung:	fetal
34	chr13:66252177-66252227	NB4	blood:	n/a
35	chr13:66878738-66878788	HEK293	kidney:	embryo
36	chr13:66583583-66583633	NT2-D1	testis:	n/a
37	chr13:67101887-67101937	BE2_C	brain:	n/a
38	chr13:66929165-66929215	GM12878	blood:	n/a
39	chr13:66878738-66878788	AG04450	lung:	fetal
40	chr13:66607275-66607325	AG09319	gingival:	n/a
41	chr13:66878738-66878788	PANC-1	pancreas:	n/a
42	chr13:67101887-67101937	MCF10A-Er-Src	breast:	n/a
43	chr13:66322551-66322601	CMK	blood:	n/a
44	chr13:66583583-66583633	HCM	heart:	n/a
45	chr13:66501111-66501161	HCPEpiC	choroid plexus:	n/a
46	chr13:66501111-66501161	AG04449	skin:	fetal
47	chr13:66322551-66322601	SKMC	muscle:	n/a
48	chr13:66981290-66981340	HCPEpiC	choroid plexus:	n/a
49	chr13:66583583-66583633	HMEC	breast:	n/a
50	chr13:66607275-66607325	SK-N-SH	brain:	n/a

(count:54 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr13:66423397..66425712-chr13:66435469..66437961,2	K562	blood:
2	chr13:66725373..66727381-chr13:66728791..66730521,2	K562	blood:
3	chr13:66377468..66378968-chr8:43092929..43094908,2	MCF-7	breast:
4	chr13:66296680..66298971-chr13:66300615..66302352,2	MCF-7	breast:
5	chr13:66918574..66921439-chr13:66945401..66948264,2	MCF-7	breast:
6	chr13:66296680..66298971-chr13:66300615..66302352,2	MCF-7	breast:
7	chr13:67109100..67110769-chr13:67114510..67116820,2	K562	blood:
8	chr13:66879908..66881972-chr13:66902872..66904425,2	K562	blood:
9	chr13:67065287..67067165-chr13:67261665..67264552,2	MCF-7	breast:
10	chr13:67124095..67126180-chr13:67127910..67129667,2	K562	blood:
11	chr13:66500564..66501578-chr13:66540848..66541721,3	MCF-7	breast:
12	chr13:66901663..66903255-chr13:66906195..66907818,2	K562	blood:
13	chr13:66582815..66585533-chr13:66632919..66634778,2	K562	blood:
14	chr13:66423397..66425712-chr13:66435469..66437961,2	K562	blood:
15	chr13:66782802..66785217-chr13:66787154..66788780,2	MCF-7	breast:
16	chr13:66782802..66785217-chr13:66787154..66788780,2	MCF-7	breast:
17	chr13:66879908..66881972-chr13:66902872..66904425,2	K562	blood:
18	chr13:66622814..66624893-chr13:66627297..66630041,2	K562	blood:
19	chr13:67109100..67110769-chr13:67114510..67116820,2	K562	blood:
20	chr13:66355137..66357196-chr13:66362374..66364366,2	K562	blood:
21	chr13:67027655..67028155-chr8:43092779..43093429,2	MCF-7	breast:
22	chr13:67118715..67120725-chr13:67121848..67124669,2	K562	blood:
23	chr13:66230680..66231446-chr13:66540896..66541772,3	MCF-7	breast:
24	chr13:67090368..67092830-chr13:67094169..67095769,2	K562	blood:
25	chr13:66918574..66921439-chr13:66945401..66948264,2	MCF-7	breast:
26	chr13:67090368..67092830-chr13:67094169..67095769,2	K562	blood:
27	chr13:66909684..66911530-chr13:66916300..66919201,2	K562	blood:
28	chr13:66557440..66557967-chr13:82054818..82055319,2	MCF-7	breast:
29	chr13:66901663..66903255-chr13:66906195..66907818,2	K562	blood:
30	chr13:66824109..66824810-chr16:71735977..71736631,2	MCF-7	breast:
31	chr13:65045929..65046727-chr13:66212514..66213321,2	MCF-7	breast:
32	chr13:66230680..66231446-chr13:66540896..66541772,3	MCF-7	breast:
33	chr13:66725373..66727381-chr13:66728791..66730521,2	K562	blood:
34	chr13:67066396..67067204-chr13:67263202..67263856,3	MCF-7	breast:
35	chr13:66909684..66911530-chr13:66916300..66919201,2	K562	blood:
36	chr13:66606276..66609107-chr13:66609295..66610970,2	MCF-7	breast:
37	chr10:29694023..29695542-chr13:67026635..67028155,2	MCF-7	breast:
38	chr13:66363582..66364363-chr21:32786060..32786817,2	MCF-7	breast:
39	chr13:66358245..66360880-chr16:71346372..71347872,2	MCF-7	breast:
40	chr13:65020257..65021157-chr13:66212532..66213123,2	MCF-7	breast:
41	chr12:28240626..28241152-chr13:66662383..66662898,2	MCF-7	breast:
42	chr13:66606276..66609107-chr13:66609295..66610970,2	MCF-7	breast:
43	chr13:66677587..66680337-chr13:66682446..66685267,2	K562	blood:
44	chr13:66978910..66981496-chr13:66983194..66984802,2	K562	blood:
45	chr13:66978910..66981496-chr13:66983194..66984802,2	K562	blood:
46	chr13:66500564..66501578-chr13:66540848..66541721,3	MCF-7	breast:
47	chr13:67065181..67066891-chr13:67075366..67077021,2	MCF-7	breast:
48	chr13:66677587..66680337-chr13:66682446..66685267,2	K562	blood:
49	chr13:67065181..67066891-chr13:67075366..67077021,2	MCF-7	breast:
50	chr13:66622814..66624893-chr13:66627297..66630041,2	K562	blood:

(count:24 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL445989.1-10	chr13:66515195-66515334	XLOC_010415
2	lnc-AL445989.1-26	chr13:66843129-66844590	NONHSAT034207
3	lnc-AL445989.1-9	chr13:66510419-66510480	XLOC_010414
4	lnc-PCDH9-1	chr13:66805874-66806206	ENSG00000250631
5	lnc-AL445989.1-13	chr13:66878003-66878146	ENSG00000234527.1
6	lnc-AL445989.1-11	chr13:66628093-66628119	XLOC_010416
7	lnc-AL445989.1-10	chr13:66546596-66551943	XLOC_010415
8	lnc-AL445989.1-11	chr13:66569993-66570140	XLOC_010416
9	lnc-AL445989.1-8	chr13:66451989-66452351	NONHSAT034197
10	lnc-AL445989.1-8	chr13:66449839-66449901	ENSG00000234767
11	lnc-PCDH9-6	chr13:66430425-66430559	NONHSAT034195
12	lnc-AL445989.1-26	chr13:66844520-66844603	NONHSAT034208
13	lnc-AL445989.1-8	chr13:66449839-66449901	NONHSAT034197
14	lnc-AL445989.1-8	chr13:66440195-66440400	NONHSAT034197
15	lnc-AL445989.1-8	chr13:66451989-66452351	ENSG00000234767
16	lnc-PCDH9-1	chr13:66718649-66718753	ENSG00000250631
17	lnc-AL445989.1-26	chr13:66851684-66852109	NONHSAT034208
18	lnc-AL445989.1-26	chr13:66846998-66847098	NONHSAT034208
19	lnc-AL445989.1-11	chr13:66569686-66569896	XLOC_010416
20	lnc-AL445989.1-8	chr13:66440306-66440375	ENSG00000234767
21	lnc-PCDH9-1	chr13:66715500-66715905	ENSG00000250631
22	lnc-AL445989.1-9	chr13:66503637-66503853	XLOC_010414
23	lnc-AL445989.1-13	chr13:66897306-66897693	ENSG00000234527.1
24	lnc-PCDH9-6	chr13:66410063-66410464	NONHSAT034195

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4704-5p	chr13:66792391-66792412	MIMAT0019803
hsa-miR-548x-3p	chr13:66540484-66540503	MIMAT0015081
hsa-miR-4704-3p	chr13:66792428-66792449	MIMAT0019804

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	PCDH9	hsa-miR-155-5p	chr13:66877756-66877779
2	PCDH9	hsa-miR-155-5p	chr13:66878321-66878343
3	PCDH9	hsa-miR-155-5p	chr13:66878327-66878320

Variant related genes	Relation type
MIR4704	TF binding region
TRIM60P19	TF binding region
PCDH9-AS1	TF binding region
LINC01052	TF binding region
MIR548X2	TF binding region
HNRNPA3P5	TF binding region
ENSG00000221685	TF binding region
MIR4704	CpG island
TRIM60P19	CpG island
PCDH9-AS1	CpG island
LINC01052	CpG island
MIR548X2	CpG island
HNRNPA3P5	CpG island
ENSG00000221685	CpG island
ENSG00000236565	chromatin interactions
INO80D	miRNA target sites

Extended variants
information (count: 18466 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:18466 , 50 per page) page: 1 2 3 4 5 6 7 ... 370

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565956306	chr13:66199485-66199486	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs574820615	chr13:66199508-66199509	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs76830803	chr13:66199613-66199614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs114557975	chr13:66199631-66199632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs572807078	chr13:66199647-66199648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs147944896	chr13:66199654-66199655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs184190389	chr13:66199655-66199656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs576116428	chr13:66199670-66199671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs530535386	chr13:66199715-66199716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs544255585	chr13:66199763-66199764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs201867366	chr13:66199823-66199824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs76496274	chr13:66199832-66199833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs398023136	chr13:66199835-66199836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs200659273	chr13:66199836-66199837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs115603066	chr13:66199849-66199850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs530058117	chr13:66199872-66199873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs73496654	chr13:66199889-66199890	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs186608336	chr13:66199979-66199980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs532474777	chr13:66199983-66199984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs73496655	chr13:66199996-66199997	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs569289540	chr13:66200017-66200018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs200971501	chr13:66200027-66200028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs3072990	chr13:66200029-66200030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs397838473	chr13:66200043-66200044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs537825814	chr13:66200051-66200052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs530115046	chr13:66200115-66200116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs554588706	chr13:66200170-66200171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs191976369	chr13:66200177-66200178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs964666	chr13:66200191-66200192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs554025873	chr13:66200209-66200210	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs577389262	chr13:66200213-66200214	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs140094699	chr13:66200229-66200230	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs560250696	chr13:66200233-66200234	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs964667	chr13:66200316-66200317	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs964668	chr13:66200362-66200363	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs575459849	chr13:66200372-66200373	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs544218509	chr13:66200378-66200379	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs74091294	chr13:66200379-66200380	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs182796498	chr13:66200383-66200384	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs187117245	chr13:66200395-66200396	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs191931005	chr13:66200396-66200397	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs532320620	chr13:66200432-66200433	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs145516018	chr13:66200441-66200442	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs569329225	chr13:66200456-66200457	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs531730508	chr13:66200494-66200495	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs200744776	chr13:66200509-66200510	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs147698703	chr13:66200531-66200532	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs182180265	chr13:66200535-66200536	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs534194530	chr13:66200536-66200537	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs554462665	chr13:66200653-66200654	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:106)

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	17133270	CNVD
Myoepithelioma	18604193	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Prostate cancer	16573809	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	17245344	CNVD
Prostate cancer	18632612	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Merkel cell carcinoma	19020549	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21858162	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Gastric cancer	17908304	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Breast cancer	17393978	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Colorectal cancer	16774939	CNVD
Adenoid cystic carcinoma	17372589	CNVD
abnormal development	18461090	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Prostate cancer	16461572	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Intellectual disability	21811512	CNVD
Colorectal cancer	21645411	CNVD
Melanoma	20877625	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:1700 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:66199400-66199600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr13:66199600-66200200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr13:66200200-66200800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr13:66200800-66204800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr13:66204800-66205200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr13:66205200-66205400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr13:66205200-66205600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr13:66205400-66205600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr13:66205600-66205800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr13:66210400-66210800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr13:66210800-66216800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr13:66216800-66217000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr13:66216800-66218000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr13:66217000-66217200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr13:66217000-66218000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr13:66217200-66217400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr13:66217400-66217800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr13:66221200-66221600	Enhancers	Fetal Brain Female	brain
19	chr13:66227400-66228200	Enhancers	Fetal Brain Male	brain
20	chr13:66227600-66228000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr13:66227800-66228400	Enhancers	Fetal Brain Female	brain
22	chr13:66231800-66232800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr13:66232000-66234000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr13:66232200-66232600	Enhancers	Adipose Nuclei	Adipose
25	chr13:66244200-66245000	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr13:66249600-66249800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr13:66251800-66252800	Enhancers	Osteobl	bone
28	chr13:66252000-66252400	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr13:66252000-66252400	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr13:66252000-66252400	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr13:66252000-66252600	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr13:66252000-66252600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr13:66252000-66252600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr13:66252200-66252600	Enhancers	Hela-S3	cervix
35	chr13:66252600-66253000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr13:66252800-66253200	Weak transcription	Osteobl	bone
37	chr13:66253000-66253600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr13:66253200-66253800	Enhancers	Osteobl	bone
39	chr13:66260600-66267000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
40	chr13:66263200-66267000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr13:66267000-66267200	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
42	chr13:66267000-66267600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr13:66267000-66267600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr13:66284600-66285200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr13:66298000-66298800	Enhancers	Dnd41	blood
46	chr13:66298200-66298600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr13:66298200-66298600	Enhancers	Fetal Stomach	stomach
48	chr13:66298200-66298800	Enhancers	Muscle Satellite Cultured Cells	--
49	chr13:66298200-66298800	Enhancers	Fetal Kidney	kidney
50	chr13:66298200-66298800	Enhancers	NHDF-Ad	bronchial

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