Variant report

Variant	nsv932195
Chromosome Location	chr13:66215786-67215733
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4001)
CpG islands
(count:1098)
Chromatin interactive
region (count:61)
LncRNA
region (count:24)
Mature miRNA
region (count: 3)
miRNA target
sites (count:3)

(count:4001 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:67024589-67024601	K562	blood:	n/a	n/a
2	ARID3A	chr13:66886857-66887028	HepG2	liver:	n/a	n/a
3	ARID3A	chr13:66784968-66784973	HepG2	liver:	n/a	n/a
4	ARID3A	chr13:67142089-67142310	K562	blood:	n/a	n/a
5	ARID3A	chr13:66651230-66651680	K562	blood:	n/a	n/a
6	ARID3A	chr13:66713473-66713809	HepG2	liver:	n/a	n/a
7	ARID3A	chr13:66648258-66648447	K562	blood:	n/a	n/a
8	ARID3A	chr13:66650602-66650906	K562	blood:	n/a	n/a
9	ARID3A	chr13:67192956-67193156	K562	blood:	n/a	n/a
10	ARID3A	chr13:66643768-66644097	K562	blood:	n/a	n/a
11	ATF1	chr13:66990708-66990955	K562	blood:	n/a	n/a
12	ATF1	chr13:66643737-66644023	K562	blood:	n/a	n/a
13	ATF1	chr13:66999986-67000196	K562	blood:	n/a	n/a
14	ATF1	chr13:66648256-66648525	K562	blood:	n/a	n/a
15	ATF1	chr13:66650593-66650896	K562	blood:	n/a	n/a
16	ATF2	chr13:66712423-66712799	GM12878	blood:	n/a	n/a
17	ATF2	chr13:66798630-66799137	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF3	chr13:66886740-66887227	A549	lung:	n/a	n/a
19	BACH1	chr13:67132673-67133003	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr13:67078100-67078397	H1-hESC	embryonic stem cell:	n/a	chr13:67078231-67078245
21	BATF	chr13:67052441-67052616	GM12878	blood:	n/a	n/a
22	BATF	chr13:66702801-66703238	GM12878	blood:	n/a	n/a
23	BATF	chr13:66712420-66712936	GM12878	blood:	n/a	n/a
24	BATF	chr13:66712465-66712951	GM12878	blood:	n/a	n/a
25	BATF	chr13:67081195-67081436	GM12878	blood:	n/a	n/a
26	BCL11A	chr13:66702875-66703088	GM12878	blood:	n/a	n/a
27	BCL11A	chr13:67159926-67160259	GM12878	blood:	n/a	n/a
28	BCL11A	chr13:66798756-66799093	H1-hESC	embryonic stem cell:	n/a	n/a
29	BCL11A	chr13:66712423-66713013	GM12878	blood:	n/a	chr13:66712844-66712853
30	BCL11A	chr13:66702751-66703109	GM12878	blood:	n/a	n/a
31	BCL11A	chr13:66712457-66712949	GM12878	blood:	n/a	chr13:66712844-66712853
32	BCL11A	chr13:66798709-66799125	H1-hESC	embryonic stem cell:	n/a	n/a
33	BCL3	chr13:66886752-66887345	A549	lung:	n/a	n/a
34	BCL3	chr13:66886608-66887994	A549	lung:	n/a	n/a
35	BCLAF1	chr13:66712465-66712857	GM12878	blood:	n/a	chr13:66712844-66712853
36	BHLHE40	chr13:66917482-66917943	K562	blood:	n/a	n/a
37	BHLHE40	chr13:66902776-66902779	K562	blood:	n/a	n/a
38	BHLHE40	chr13:66712457-66712998	GM12878	blood:	n/a	n/a
39	BHLHE40	chr13:66648396-66648557	K562	blood:	n/a	n/a
40	BHLHE40	chr13:66739043-66739104	K562	blood:	n/a	n/a
41	BHLHE40	chr13:67214443-67214833	GM12878	blood:	n/a	n/a
42	BRCA1	chr13:66878245-66878246	Hela-S3	cervix:	n/a	n/a
43	BRCA1	chr13:66712793-66712993	GM12878	blood:	n/a	n/a
44	BRCA1	chr13:67088395-67088424	H1-hESC	embryonic stem cell:	n/a	n/a
45	CBX3	chr13:66784811-66785347	HCT-116	colon:	n/a	n/a
46	CBX3	chr13:67137257-67137558	K562	blood:	n/a	n/a
47	CBX3	chr13:66643667-66644035	K562	blood:	n/a	n/a
48	CBX3	chr13:66784784-66785224	HCT-116	colon:	n/a	n/a
49	CBX3	chr13:66861033-66861253	K562	blood:	n/a	n/a
50	CCNT2	chr13:67142117-67142330	K562	blood:	n/a	n/a

(count:1098 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:66919912-66919962	HRPEpiC	eye:	n/a
2	chr13:67197277-67197327	BJ	skin:	n/a
3	chr13:67197133-67197183	PFSK-1	brain:	n/a
4	chr13:66919912-66919962	SK-N-SH	brain:	n/a
5	chr13:66583583-66583633	Caco-2	colon:	n/a
6	chr13:67197277-67197327	A549	lung:	n/a
7	chr13:66919912-66919962	GM19239	blood:	n/a
8	chr13:66607275-66607325	Caco-2	colon:	n/a
9	chr13:67197277-67197327	K562	blood:	n/a
10	chr13:66252177-66252227	IMR90	lung:	fetal
11	chr13:66252177-66252227	AG09309	skin:	n/a
12	chr13:67155091-67155141	LNCaP	prostate:	n/a
13	chr13:67101887-67101937	AoSMC	blood vessel:	n/a
14	chr13:66322551-66322601	HRE	kidney:	n/a
15	chr13:66983676-66983726	PANC-1	pancreas:	n/a
16	chr13:66322551-66322601	SK-N-MC	brain:	n/a
17	chr13:67197173-67197223	HAEpiC	amniotic membrane:	n/a
18	chr13:66929165-66929215	HEK293	kidney:	embryo
19	chr13:66878738-66878788	HEEpiC	esophagus:	n/a
20	chr13:66501111-66501161	AG04449	skin:	fetal
21	chr13:67101887-67101937	AG10803	skin:	n/a
22	chr13:66981290-66981340	PANC-1	pancreas:	n/a
23	chr13:67101887-67101937	HMEC	breast:	n/a
24	chr13:66981290-66981340	HAEpiC	amniotic membrane:	n/a
25	chr13:67197133-67197183	GM12892	blood:	n/a
26	chr13:67101887-67101937	GM12891	blood:	n/a
27	chr13:66607275-66607325	HEEpiC	esophagus:	n/a
28	chr13:66919912-66919962	Caco-2	colon:	n/a
29	chr13:67197173-67197223	AG04449	skin:	fetal
30	chr13:66501111-66501161	NHDF-neo	bronchial:	n/a
31	chr13:66983676-66983726	HIPEpiC	eye:	n/a
32	chr13:67197277-67197327	NHBE	bronchial:	n/a
33	chr13:66983676-66983726	AG04449	skin:	fetal
34	chr13:67196386-67196436	SAEC	small airway:	n/a
35	chr13:67196386-67196436	HMEC	breast:	n/a
36	chr13:66981290-66981340	BJ	skin:	n/a
37	chr13:66919912-66919962	GM12878	blood:	n/a
38	chr13:66252177-66252227	SK-N-SH_RA	brain:	n/a
39	chr13:67196386-67196436	HL-60	blood:	n/a
40	chr13:67196386-67196436	HCPEpiC	choroid plexus:	n/a
41	chr13:66322551-66322601	RPTEC	kidney:	n/a
42	chr13:67197277-67197327	GM06990	blood:	n/a
43	chr13:67197133-67197183	NH-A	brain:	n/a
44	chr13:67197133-67197183	SK-N-SH	brain:	n/a
45	chr13:66583686-66583736	HNPCEpiC	eye:	n/a
46	chr13:66583686-66583736	GM12878	blood:	n/a
47	chr13:66919912-66919962	BE2_C	brain:	n/a
48	chr13:66983730-66983780	Hepatocyte	liver:	n/a
49	chr13:66583686-66583736	A549	lung:	n/a
50	chr13:66322551-66322601	NB4	blood:	n/a

(count:61 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr13:66782802..66785217-chr13:66787154..66788780,2	MCF-7	breast:
2	chr13:66363582..66364363-chr21:32786060..32786817,2	MCF-7	breast:
3	chr13:66606276..66609107-chr13:66609295..66610970,2	MCF-7	breast:
4	chr13:67157975..67159957-chr13:67162075..67164465,2	K562	blood:
5	chr13:66230680..66231446-chr13:66540896..66541772,3	MCF-7	breast:
6	chr13:67130437..67132993-chr13:67135417..67138774,3	K562	blood:
7	chr13:66377468..66378968-chr8:43092929..43094908,2	MCF-7	breast:
8	chr13:67118715..67120725-chr13:67121848..67124669,2	K562	blood:
9	chr12:28240626..28241152-chr13:66662383..66662898,2	MCF-7	breast:
10	chr13:66355137..66357196-chr13:66362374..66364366,2	K562	blood:
11	chr13:67066396..67067204-chr13:67263202..67263856,3	MCF-7	breast:
12	chr13:66606276..66609107-chr13:66609295..66610970,2	MCF-7	breast:
13	chr13:67124095..67126180-chr13:67127910..67129667,2	K562	blood:
14	chr13:66901663..66903255-chr13:66906195..66907818,2	K562	blood:
15	chr13:66879908..66881972-chr13:66902872..66904425,2	K562	blood:
16	chr13:67118715..67120725-chr13:67121848..67124669,2	K562	blood:
17	chr13:66978910..66981496-chr13:66983194..66984802,2	K562	blood:
18	chr13:66677587..66680337-chr13:66682446..66685267,2	K562	blood:
19	chr13:66677587..66680337-chr13:66682446..66685267,2	K562	blood:
20	chr13:67124095..67126180-chr13:67127910..67129667,2	K562	blood:
21	chr13:66423397..66425712-chr13:66435469..66437961,2	K562	blood:
22	chr13:66557440..66557967-chr13:82054818..82055319,2	MCF-7	breast:
23	chr13:67130453..67132993-chr13:67135238..67136917,2	K562	blood:
24	chr13:66296680..66298971-chr13:66300615..66302352,2	MCF-7	breast:
25	chr13:67065287..67067165-chr13:67261665..67264552,2	MCF-7	breast:
26	chr13:67090368..67092830-chr13:67094169..67095769,2	K562	blood:
27	chr13:66500564..66501578-chr13:66540848..66541721,3	MCF-7	breast:
28	chr10:29694023..29695542-chr13:67026635..67028155,2	MCF-7	breast:
29	chr13:67130437..67132993-chr13:67135417..67138774,3	K562	blood:
30	chr13:67194212..67196284-chr13:67201796..67203435,2	MCF-7	breast:
31	chr13:66622814..66624893-chr13:66627297..66630041,2	K562	blood:
32	chr13:67130453..67132993-chr13:67135238..67136917,2	K562	blood:
33	chr13:66423397..66425712-chr13:66435469..66437961,2	K562	blood:
34	chr13:66500564..66501578-chr13:66540848..66541721,3	MCF-7	breast:
35	chr13:66824109..66824810-chr16:71735977..71736631,2	MCF-7	breast:
36	chr13:67065181..67066891-chr13:67075366..67077021,2	MCF-7	breast:
37	chr13:67157975..67159957-chr13:67162075..67164465,2	K562	blood:
38	chr13:66296680..66298971-chr13:66300615..66302352,2	MCF-7	breast:
39	chr13:67027655..67028155-chr8:43092779..43093429,2	MCF-7	breast:
40	chr13:67204110..67206444-chr13:67209007..67211337,2	K562	blood:
41	chr13:66725373..66727381-chr13:66728791..66730521,2	K562	blood:
42	chr13:66879908..66881972-chr13:66902872..66904425,2	K562	blood:
43	chr13:66782802..66785217-chr13:66787154..66788780,2	MCF-7	breast:
44	chr13:66909684..66911530-chr13:66916300..66919201,2	K562	blood:
45	chr13:67109100..67110769-chr13:67114510..67116820,2	K562	blood:
46	chr13:66909684..66911530-chr13:66916300..66919201,2	K562	blood:
47	chr13:67090368..67092830-chr13:67094169..67095769,2	K562	blood:
48	chr13:66622814..66624893-chr13:66627297..66630041,2	K562	blood:
49	chr13:66582815..66585533-chr13:66632919..66634778,2	K562	blood:
50	chr13:67194212..67196284-chr13:67201796..67203435,2	MCF-7	breast:

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

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

miRNA name	Chromosome Location	mirBase accession
hsa-miR-548x-3p	chr13:66540484-66540503	MIMAT0015081
hsa-miR-4704-5p	chr13:66792391-66792412	MIMAT0019803
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	chr13:66878321-66878343
2	PCDH9	hsa-miR-155-5p	chr13:66878327-66878320
3	PCDH9	hsa-miR-155-5p	chr13:66877756-66877779

Variant related genes	Relation type
MIR4704	TF binding region
RNU7-87P	TF binding region
MIR548X2	TF binding region
TRIM60P19	TF binding region
HNRNPA3P5	TF binding region
PCDH9-AS1	TF binding region
ENSG00000221685	TF binding region
LINC01052	TF binding region
MIR4704	CpG island
RNU7-87P	CpG island
MIR548X2	CpG island
TRIM60P19	CpG island
HNRNPA3P5	CpG island
PCDH9-AS1	CpG island
ENSG00000221685	CpG island
LINC01052	CpG island
ENSG00000236565	chromatin interactions
ENSG00000238500	chromatin interactions
INO80D	miRNA target sites

Extended variants
information (count: 19862 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:19862 , 50 per page) page: 1 2 3 4 5 6 7 ... 398

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185243281	chr13:66215806-66215807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs571699158	chr13:66215838-66215839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs537447193	chr13:66215880-66215881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs560513306	chr13:66215894-66215895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs567903965	chr13:66215940-66215941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs200241169	chr13:66215989-66215990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs7326838	chr13:66216011-66216012	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs548278594	chr13:66216125-66216126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs553118907	chr13:66216145-66216146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs573733439	chr13:66216150-66216151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs573086764	chr13:66216181-66216182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs138968096	chr13:66216183-66216184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs11840518	chr13:66216190-66216191	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs73195803	chr13:66216225-66216226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs117261841	chr13:66216278-66216279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs17545555	chr13:66216379-66216380	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs190019843	chr13:66216411-66216412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs181095398	chr13:66216415-66216416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs200939021	chr13:66216421-66216422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs202001064	chr13:66216422-66216423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs142083174	chr13:66216428-66216429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs35533302	chr13:66216434-66216435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs63404963	chr13:66216439-66216440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs3072994	chr13:66216449-66216450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs374451228	chr13:66216450-66216451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs367989086	chr13:66216451-66216452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs559709150	chr13:66216499-66216500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs372397203	chr13:66216504-66216505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs149676838	chr13:66216570-66216571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs528294738	chr13:66216610-66216611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs369080688	chr13:66216662-66216663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs9540497	chr13:66216701-66216702	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs186450505	chr13:66216724-66216725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs530914509	chr13:66216741-66216742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs537844419	chr13:66216760-66216761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs74977442	chr13:66216875-66216876	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs567568321	chr13:66216878-66216879	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs368557241	chr13:66216888-66216889	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs149428814	chr13:66216893-66216894	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs188007026	chr13:66216924-66216925	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs538807910	chr13:66216966-66216967	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs550774725	chr13:66216968-66216969	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs577637639	chr13:66216978-66216979	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs549718643	chr13:66216985-66216986	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs536760510	chr13:66217005-66217006	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs143789667	chr13:66217022-66217023	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs573654302	chr13:66217036-66217037	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs568451824	chr13:66217053-66217054	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs527485223	chr13:66217059-66217060	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs113871553	chr13:66217060-66217061	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:108)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Myelofibrosis	22110671	CNVD

Chromatin state (count:1899 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:66216800-66217000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr13:66216800-66218000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr13:66217000-66217200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr13:66217000-66218000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr13:66217200-66217400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr13:66217400-66217800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr13:66221200-66221600	Enhancers	Fetal Brain Female	brain
8	chr13:66227400-66228200	Enhancers	Fetal Brain Male	brain
9	chr13:66227600-66228000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr13:66227800-66228400	Enhancers	Fetal Brain Female	brain
11	chr13:66231800-66232800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr13:66232000-66234000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr13:66232200-66232600	Enhancers	Adipose Nuclei	Adipose
14	chr13:66244200-66245000	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr13:66249600-66249800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr13:66251800-66252800	Enhancers	Osteobl	bone
17	chr13:66252000-66252400	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr13:66252000-66252400	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr13:66252000-66252400	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr13:66252000-66252600	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr13:66252000-66252600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr13:66252000-66252600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr13:66252200-66252600	Enhancers	Hela-S3	cervix
24	chr13:66252600-66253000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr13:66252800-66253200	Weak transcription	Osteobl	bone
26	chr13:66253000-66253600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr13:66253200-66253800	Enhancers	Osteobl	bone
28	chr13:66260600-66267000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
29	chr13:66263200-66267000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr13:66267000-66267200	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
31	chr13:66267000-66267600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr13:66267000-66267600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr13:66284600-66285200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr13:66298000-66298800	Enhancers	Dnd41	blood
35	chr13:66298200-66298600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr13:66298200-66298600	Enhancers	Fetal Stomach	stomach
37	chr13:66298200-66298800	Enhancers	Muscle Satellite Cultured Cells	--
38	chr13:66298200-66298800	Enhancers	Fetal Kidney	kidney
39	chr13:66298200-66298800	Enhancers	NHDF-Ad	bronchial
40	chr13:66298200-66299400	Enhancers	Fetal Lung	lung
41	chr13:66298200-66299800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr13:66298200-66300200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr13:66298800-66299200	Weak transcription	Fetal Kidney	kidney
44	chr13:66299200-66299800	Enhancers	Fetal Kidney	kidney
45	chr13:66299400-66299800	Enhancers	Fetal Heart	heart
46	chr13:66307000-66307600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr13:66318200-66319600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr13:66318400-66318800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr13:66318400-66319600	Enhancers	Osteobl	bone
50	chr13:66318800-66319000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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