Variant report

Variant	nsv534503
Chromosome Location	chr13:66287963-67126195
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3244)
CpG islands
(count:733)
Chromatin interactive
region (count:49)
LncRNA
region (count:24)
Mature miRNA
region (count: 3)
miRNA target
sites (count:3)

(count:3244 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:66713473-66713809	HepG2	liver:	n/a	n/a
2	ARID3A	chr13:66643768-66644097	K562	blood:	n/a	n/a
3	ARID3A	chr13:66784968-66784973	HepG2	liver:	n/a	n/a
4	ARID3A	chr13:67024589-67024601	K562	blood:	n/a	n/a
5	ARID3A	chr13:66886857-66887028	HepG2	liver:	n/a	n/a
6	ARID3A	chr13:66651230-66651680	K562	blood:	n/a	n/a
7	ARID3A	chr13:66650602-66650906	K562	blood:	n/a	n/a
8	ARID3A	chr13:66648258-66648447	K562	blood:	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	chr13:66643737-66644023	K562	blood:	n/a	n/a
12	ATF1	chr13:66999986-67000196	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	chr13:67081195-67081436	GM12878	blood:	n/a	n/a
19	BATF	chr13:66702801-66703238	GM12878	blood:	n/a	n/a
20	BATF	chr13:66712420-66712936	GM12878	blood:	n/a	n/a
21	BATF	chr13:66712465-66712951	GM12878	blood:	n/a	n/a
22	BATF	chr13:67052441-67052616	GM12878	blood:	n/a	n/a
23	BCL11A	chr13:66702751-66703109	GM12878	blood:	n/a	n/a
24	BCL11A	chr13:66702875-66703088	GM12878	blood:	n/a	n/a
25	BCL11A	chr13:66798756-66799093	H1-hESC	embryonic stem cell:	n/a	n/a
26	BCL11A	chr13:66712457-66712949	GM12878	blood:	n/a	chr13:66712844-66712853
27	BCL11A	chr13:66712423-66713013	GM12878	blood:	n/a	chr13:66712844-66712853
28	BCL11A	chr13:66798709-66799125	H1-hESC	embryonic stem cell:	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	chr13:66739043-66739104	K562	blood:	n/a	n/a
33	BHLHE40	chr13:66902776-66902779	K562	blood:	n/a	n/a
34	BHLHE40	chr13:66712457-66712998	GM12878	blood:	n/a	n/a
35	BHLHE40	chr13:66648396-66648557	K562	blood:	n/a	n/a
36	BHLHE40	chr13:66917482-66917943	K562	blood:	n/a	n/a
37	BRCA1	chr13:66712793-66712993	GM12878	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	CBX3	chr13:66861033-66861253	K562	blood:	n/a	n/a
41	CBX3	chr13:66643667-66644035	K562	blood:	n/a	n/a
42	CBX3	chr13:66784784-66785224	HCT-116	colon:	n/a	n/a
43	CBX3	chr13:66784811-66785347	HCT-116	colon:	n/a	n/a
44	CCNT2	chr13:66589547-66589747	K562	blood:	n/a	n/a
45	CCNT2	chr13:66617039-66617239	K562	blood:	n/a	n/a
46	CEBPB	chr13:66487605-66487805	A549	lung:	n/a	n/a
47	CEBPB	chr13:66405298-66405623	IMR90	lung:	n/a	chr13:66405470-66405481
48	CEBPB	chr13:66888568-66888896	A549	lung:	n/a	n/a
49	CEBPB	chr13:66840058-66840316	IMR90	lung:	n/a	chr13:66840131-66840144 chr13:66840121-66840133
50	CEBPB	chr13:66491284-66491489	HepG2	liver:	n/a	chr13:66491416-66491427 chr13:66491415-66491426

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:66983730-66983780	LNCaP	prostate:	n/a
2	chr13:66983730-66983780	LNCaP	prostate:	n/a
3	chr13:66583686-66583736	AG10803	skin:	n/a
4	chr13:66983730-66983780	SK-N-MC	brain:	n/a
5	chr13:66501111-66501161	AG04449	skin:	fetal
6	chr13:66322551-66322601	AG04450	lung:	fetal
7	chr13:66919912-66919962	H1-hESC	embryonic stem cell:	embryo
8	chr13:66607275-66607325	HCT-116	colon:	n/a
9	chr13:67101887-67101937	SK-N-SH_RA	brain:	n/a
10	chr13:66501111-66501161	RPTEC	kidney:	n/a
11	chr13:66878738-66878788	SAEC	small airway:	n/a
12	chr13:66983730-66983780	NHDF-neo	bronchial:	n/a
13	chr13:66322551-66322601	Hepatocyte	liver:	n/a
14	chr13:66501111-66501161	HUVEC	blood vessel:	n/a
15	chr13:66583583-66583633	PANC-1	pancreas:	n/a
16	chr13:66981290-66981340	ovcar-3	ovarian:	n/a
17	chr13:66983676-66983726	HIPEpiC	eye:	n/a
18	chr13:66929165-66929215	SK-N-SH_RA	brain:	n/a
19	chr13:66983676-66983726	HAEpiC	amniotic membrane:	n/a
20	chr13:66983676-66983726	K562	blood:	n/a
21	chr13:66983730-66983780	GM12878	blood:	n/a
22	chr13:66983676-66983726	HRPEpiC	eye:	n/a
23	chr13:66981290-66981340	NHBE	bronchial:	n/a
24	chr13:66878738-66878788	AoSMC	blood vessel:	n/a
25	chr13:66929165-66929215	AG09309	skin:	n/a
26	chr13:66878738-66878788	U87	brain:	n/a
27	chr13:67101887-67101937	AoSMC	blood vessel:	n/a
28	chr13:66878738-66878788	HPAEpiC	pulmonary alveolar:	n/a
29	chr13:66322551-66322601	HEK293	kidney:	embryo
30	chr13:66322551-66322601	HepG2	liver:	n/a
31	chr13:66583583-66583633	NHBE	bronchial:	n/a
32	chr13:66919912-66919962	GM12891	blood:	n/a
33	chr13:66981290-66981340	HRE	kidney:	n/a
34	chr13:66583583-66583633	Jurkat	blood:	n/a
35	chr13:66322551-66322601	CMK	blood:	n/a
36	chr13:66983676-66983726	CMK	blood:	n/a
37	chr13:66583686-66583736	HCPEpiC	choroid plexus:	n/a
38	chr13:66929165-66929215	HCM	heart:	n/a
39	chr13:66583686-66583736	SKMC	muscle:	n/a
40	chr13:66583583-66583633	SAEC	small airway:	n/a
41	chr13:66929165-66929215	Jurkat	blood:	n/a
42	chr13:66981290-66981340	U87	brain:	n/a
43	chr13:66583583-66583633	U87	brain:	n/a
44	chr13:66983676-66983726	T-47D	breast:	n/a
45	chr13:66583686-66583736	AG09319	gingival:	n/a
46	chr13:66983676-66983726	HCF	heart:	n/a
47	chr13:66322551-66322601	BJ	skin:	n/a
48	chr13:66983730-66983780	NB4	blood:	n/a
49	chr13:66919912-66919962	T-47D	breast:	n/a
50	chr13:66583686-66583736	AG04449	skin:	fetal

(count:49 , 50 per page) page: 1

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

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PCDH9-6	chr13:66430425-66430559	NONHSAT034195
2	lnc-PCDH9-1	chr13:66805874-66806206	ENSG00000250631
3	lnc-AL445989.1-8	chr13:66451989-66452351	ENSG00000234767
4	lnc-AL445989.1-26	chr13:66843129-66844590	NONHSAT034207
5	lnc-AL445989.1-10	chr13:66515195-66515334	XLOC_010415
6	lnc-AL445989.1-13	chr13:66878003-66878146	ENSG00000234527.1
7	lnc-AL445989.1-11	chr13:66628093-66628119	XLOC_010416
8	lnc-PCDH9-1	chr13:66715500-66715905	ENSG00000250631
9	lnc-AL445989.1-8	chr13:66449839-66449901	ENSG00000234767
10	lnc-AL445989.1-26	chr13:66846998-66847098	NONHSAT034208
11	lnc-AL445989.1-9	chr13:66510419-66510480	XLOC_010414
12	lnc-AL445989.1-26	chr13:66851684-66852109	NONHSAT034208
13	lnc-PCDH9-1	chr13:66718649-66718753	ENSG00000250631
14	lnc-AL445989.1-13	chr13:66897306-66897693	ENSG00000234527.1
15	lnc-AL445989.1-8	chr13:66449839-66449901	NONHSAT034197
16	lnc-AL445989.1-8	chr13:66440306-66440375	ENSG00000234767
17	lnc-AL445989.1-8	chr13:66440195-66440400	NONHSAT034197
18	lnc-AL445989.1-8	chr13:66451989-66452351	NONHSAT034197
19	lnc-AL445989.1-11	chr13:66569686-66569896	XLOC_010416
20	lnc-AL445989.1-26	chr13:66844520-66844603	NONHSAT034208
21	lnc-AL445989.1-10	chr13:66546596-66551943	XLOC_010415
22	lnc-AL445989.1-9	chr13:66503637-66503853	XLOC_010414
23	lnc-AL445989.1-11	chr13:66569993-66570140	XLOC_010416
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	chr13:66878327-66878320
2	PCDH9	hsa-miR-155-5p	chr13:66878321-66878343
3	PCDH9	hsa-miR-155-5p	chr13:66877756-66877779

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: 17275 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:17275 , 50 per page) page: 1 2 3 4 5 6 7 ... 346

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549161686	chr13:66298132-66298133	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs566213617	chr13:66298146-66298147	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs189171760	chr13:66298152-66298153	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs375424063	chr13:66298160-66298161	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs541490992	chr13:66298177-66298178	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs4098535	chr13:66298181-66298182	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs571951006	chr13:66298183-66298184	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs537709480	chr13:66298185-66298186	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs373182647	chr13:66298273-66298274	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs182150090	chr13:66298289-66298290	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs574109889	chr13:66298320-66298321	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs536855295	chr13:66298350-66298351	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs116457653	chr13:66298360-66298361	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs571848688	chr13:66298364-66298365	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs578094972	chr13:66298371-66298372	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs540608023	chr13:66298383-66298384	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs563766827	chr13:66298436-66298437	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs186865844	chr13:66298458-66298459	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs543273157	chr13:66298467-66298468	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs563604276	chr13:66298504-66298505	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs7992551	chr13:66298543-66298544	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs549202868	chr13:66298626-66298627	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs74789345	chr13:66298628-66298629	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs528627963	chr13:66298638-66298639	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs372506088	chr13:66298657-66298658	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs563689043	chr13:66298667-66298668	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs551929471	chr13:66298669-66298670	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs9571466	chr13:66298690-66298691	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs537448036	chr13:66298698-66298699	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs550944712	chr13:66298709-66298710	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs567993439	chr13:66298722-66298723	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs536434044	chr13:66298738-66298739	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs543050186	chr13:66298758-66298759	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs144408296	chr13:66298760-66298761	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs377651745	chr13:66298764-66298765	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs190057995	chr13:66298778-66298779	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs534385800	chr13:66298797-66298798	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs557441169	chr13:66298798-66298799	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs182126907	chr13:66298801-66298802	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs529918573	chr13:66298805-66298806	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs143139948	chr13:66298813-66298814	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs185608840	chr13:66298816-66298817	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs190425801	chr13:66298819-66298820	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs542439573	chr13:66298839-66298840	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs146403343	chr13:66298860-66298861	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs377643820	chr13:66298868-66298869	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs370148343	chr13:66298920-66298921	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs528308870	chr13:66298939-66298940	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs370859763	chr13:66298985-66298986	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs551855517	chr13:66298986-66298987	Enhancers Weak transcription	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:1656 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:66298000-66298800	Enhancers	Dnd41	blood
2	chr13:66298200-66298600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr13:66298200-66298600	Enhancers	Fetal Stomach	stomach
4	chr13:66298200-66298800	Enhancers	Muscle Satellite Cultured Cells	--
5	chr13:66298200-66298800	Enhancers	Fetal Kidney	kidney
6	chr13:66298200-66298800	Enhancers	NHDF-Ad	bronchial
7	chr13:66298200-66299400	Enhancers	Fetal Lung	lung
8	chr13:66298200-66299800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr13:66298200-66300200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr13:66298800-66299200	Weak transcription	Fetal Kidney	kidney
11	chr13:66299200-66299800	Enhancers	Fetal Kidney	kidney
12	chr13:66299400-66299800	Enhancers	Fetal Heart	heart
13	chr13:66307000-66307600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr13:66318200-66319600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr13:66318400-66318800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr13:66318400-66319600	Enhancers	Osteobl	bone
17	chr13:66318800-66319000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr13:66318800-66319400	Enhancers	Adipose Nuclei	Adipose
19	chr13:66318800-66320600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr13:66319000-66319600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr13:66330600-66331400	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
22	chr13:66336600-66337200	Enhancers	Fetal Kidney	kidney
23	chr13:66342600-66343200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr13:66343000-66343400	Enhancers	H1 Cell Line	embryonic stem cell
25	chr13:66343000-66343400	Active TSS	iPS-20b Cell Line	embryonic stem cell
26	chr13:66347000-66347200	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr13:66347200-66349800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr13:66357600-66358000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr13:66358000-66358400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr13:66363800-66364200	Enhancers	Osteobl	bone
31	chr13:66363800-66364600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr13:66363800-66364600	Enhancers	Muscle Satellite Cultured Cells	--
33	chr13:66363800-66364600	Enhancers	HSMMtube	muscle
34	chr13:66364200-66364600	Flanking Active TSS	Osteobl	bone
35	chr13:66372000-66373600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr13:66373600-66376400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr13:66376400-66377200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr13:66376600-66377000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr13:66377000-66379000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr13:66377200-66379000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr13:66379000-66379200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr13:66379000-66379400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr13:66379200-66379600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr13:66379400-66382200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr13:66379600-66379800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr13:66379800-66382400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr13:66380800-66382000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr13:66381000-66382800	Enhancers	Muscle Satellite Cultured Cells	--
49	chr13:66381000-66382800	Enhancers	Osteobl	bone
50	chr13:66381400-66383200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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