Variant report

Variant	nsv1052017
Chromosome Location	chr13:66232288-67213033
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3810)
CpG islands
(count:1099)
Chromatin interactive
region (count:59)
LncRNA
region (count:24)
Mature miRNA
region (count: 3)
miRNA target
sites (count:3)

(count:3810 , 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	chr13:66784968-66784973	HepG2	liver:	n/a	n/a
2	ARID3A	chr13:67024589-67024601	K562	blood:	n/a	n/a
3	ARID3A	chr13:66648258-66648447	K562	blood:	n/a	n/a
4	ARID3A	chr13:66651230-66651680	K562	blood:	n/a	n/a
5	ARID3A	chr13:66650602-66650906	K562	blood:	n/a	n/a
6	ARID3A	chr13:67142089-67142310	K562	blood:	n/a	n/a
7	ARID3A	chr13:66643768-66644097	K562	blood:	n/a	n/a
8	ARID3A	chr13:66713473-66713809	HepG2	liver:	n/a	n/a
9	ARID3A	chr13:67192956-67193156	K562	blood:	n/a	n/a
10	ARID3A	chr13:66886857-66887028	HepG2	liver:	n/a	n/a
11	ATF1	chr13:66648256-66648525	K562	blood:	n/a	n/a
12	ATF1	chr13:66990708-66990955	K562	blood:	n/a	n/a
13	ATF1	chr13:66999986-67000196	K562	blood:	n/a	n/a
14	ATF1	chr13:66650593-66650896	K562	blood:	n/a	n/a
15	ATF1	chr13:66643737-66644023	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	chr13:67081195-67081436	GM12878	blood:	n/a	n/a
23	BATF	chr13:66712420-66712936	GM12878	blood:	n/a	n/a
24	BATF	chr13:66702801-66703238	GM12878	blood:	n/a	n/a
25	BATF	chr13:66712465-66712951	GM12878	blood:	n/a	n/a
26	BCL11A	chr13:66798709-66799125	H1-hESC	embryonic stem cell:	n/a	n/a
27	BCL11A	chr13:67159926-67160259	GM12878	blood:	n/a	n/a
28	BCL11A	chr13:66712423-66713013	GM12878	blood:	n/a	chr13:66712844-66712853
29	BCL11A	chr13:66712457-66712949	GM12878	blood:	n/a	chr13:66712844-66712853
30	BCL11A	chr13:66702751-66703109	GM12878	blood:	n/a	n/a
31	BCL11A	chr13:66702875-66703088	GM12878	blood:	n/a	n/a
32	BCL11A	chr13:66798756-66799093	H1-hESC	embryonic stem cell:	n/a	n/a
33	BCL3	chr13:66886608-66887994	A549	lung:	n/a	n/a
34	BCL3	chr13:66886752-66887345	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	chr13:66648396-66648557	K562	blood:	n/a	n/a
38	BHLHE40	chr13:66712457-66712998	GM12878	blood:	n/a	n/a
39	BHLHE40	chr13:66902776-66902779	K562	blood:	n/a	n/a
40	BHLHE40	chr13:66739043-66739104	K562	blood:	n/a	n/a
41	BRCA1	chr13:66712793-66712993	GM12878	blood:	n/a	n/a
42	BRCA1	chr13:67088395-67088424	H1-hESC	embryonic stem cell:	n/a	n/a
43	BRCA1	chr13:66878245-66878246	Hela-S3	cervix:	n/a	n/a
44	CBX3	chr13:66861033-66861253	K562	blood:	n/a	n/a
45	CBX3	chr13:66784784-66785224	HCT-116	colon:	n/a	n/a
46	CBX3	chr13:66784811-66785347	HCT-116	colon:	n/a	n/a
47	CBX3	chr13:66643667-66644035	K562	blood:	n/a	n/a
48	CBX3	chr13:67137257-67137558	K562	blood:	n/a	n/a
49	CCNT2	chr13:67142117-67142330	K562	blood:	n/a	n/a
50	CCNT2	chr13:66617039-66617239	K562	blood:	n/a	n/a

(count:1099 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:66981290-66981340	HRCEpiC	kidney:	n/a
2	chr13:66981290-66981340	HRCEpiC	kidney:	n/a
3	chr13:67155091-67155141	AG09309	skin:	n/a
4	chr13:66583583-66583633	BE2_C	brain:	n/a
5	chr13:67196386-67196436	SKMC	muscle:	n/a
6	chr13:67197173-67197223	PFSK-1	brain:	n/a
7	chr13:67197133-67197183	GM06990	blood:	n/a
8	chr13:66501111-66501161	SAEC	small airway:	n/a
9	chr13:66583686-66583736	RPTEC	kidney:	n/a
10	chr13:66252177-66252227	GM12878	blood:	n/a
11	chr13:67197133-67197183	T-47D	breast:	n/a
12	chr13:66583686-66583736	HCF	heart:	n/a
13	chr13:66983730-66983780	AG10803	skin:	n/a
14	chr13:66981290-66981340	MCF-7	breast:	n/a
15	chr13:66501111-66501161	ovcar-3	ovarian:	n/a
16	chr13:66919912-66919962	NHBE	bronchial:	n/a
17	chr13:66501111-66501161	HEEpiC	esophagus:	n/a
18	chr13:66322551-66322601	HMEC	breast:	n/a
19	chr13:66878738-66878788	SK-N-SH	brain:	n/a
20	chr13:67197173-67197223	ECC-1	luminal epithelium:	n/a
21	chr13:67197133-67197183	HCF	heart:	n/a
22	chr13:67101887-67101937	GM12891	blood:	n/a
23	chr13:67196386-67196436	Hepatocyte	liver:	n/a
24	chr13:66983730-66983780	AoSMC	blood vessel:	n/a
25	chr13:67101887-67101937	HCM	heart:	n/a
26	chr13:66322551-66322601	HEEpiC	esophagus:	n/a
27	chr13:67197133-67197183	AG04449	skin:	fetal
28	chr13:66983676-66983726	MCF10A-Er-Src	breast:	n/a
29	chr13:66501111-66501161	HPAEpiC	pulmonary alveolar:	n/a
30	chr13:67101887-67101937	ECC-1	luminal epithelium:	n/a
31	chr13:67197277-67197327	RPTEC	kidney:	n/a
32	chr13:66583583-66583633	HEEpiC	esophagus:	n/a
33	chr13:67101887-67101937	A549	lung:	n/a
34	chr13:66322551-66322601	BE2_C	brain:	n/a
35	chr13:66983730-66983780	SK-N-SH	brain:	n/a
36	chr13:66983676-66983726	HRPEpiC	eye:	n/a
37	chr13:67197277-67197327	HRPEpiC	eye:	n/a
38	chr13:66878738-66878788	PrEC	prostate:	n/a
39	chr13:66929165-66929215	HRCEpiC	kidney:	n/a
40	chr13:66983676-66983726	GM19239	blood:	n/a
41	chr13:66583686-66583736	PANC-1	pancreas:	n/a
42	chr13:66919912-66919962	U87	brain:	n/a
43	chr13:66322551-66322601	ProgFib	skin:	n/a
44	chr13:66607275-66607325	AoSMC	blood vessel:	n/a
45	chr13:66981290-66981340	NB4	blood:	n/a
46	chr13:66878738-66878788	Hepatocyte	liver:	n/a
47	chr13:66919912-66919962	ProgFib	skin:	n/a
48	chr13:66501111-66501161	HUVEC	blood vessel:	n/a
49	chr13:67197133-67197183	HRPEpiC	eye:	n/a
50	chr13:66583686-66583736	GM19239	blood:	n/a

(count:59 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr13:66582815..66585533-chr13:66632919..66634778,2	K562	blood:
2	chr13:67090368..67092830-chr13:67094169..67095769,2	K562	blood:
3	chr13:66901663..66903255-chr13:66906195..66907818,2	K562	blood:
4	chr13:66606276..66609107-chr13:66609295..66610970,2	MCF-7	breast:
5	chr13:66918574..66921439-chr13:66945401..66948264,2	MCF-7	breast:
6	chr13:66909684..66911530-chr13:66916300..66919201,2	K562	blood:
7	chr13:67130437..67132993-chr13:67135417..67138774,3	K562	blood:
8	chr13:66918574..66921439-chr13:66945401..66948264,2	MCF-7	breast:
9	chr13:67065181..67066891-chr13:67075366..67077021,2	MCF-7	breast:
10	chr13:66901663..66903255-chr13:66906195..66907818,2	K562	blood:
11	chr13:66782802..66785217-chr13:66787154..66788780,2	MCF-7	breast:
12	chr13:67194212..67196284-chr13:67201796..67203435,2	MCF-7	breast:
13	chr13:67109100..67110769-chr13:67114510..67116820,2	K562	blood:
14	chr13:66296680..66298971-chr13:66300615..66302352,2	MCF-7	breast:
15	chr13:66879908..66881972-chr13:66902872..66904425,2	K562	blood:
16	chr13:66725373..66727381-chr13:66728791..66730521,2	K562	blood:
17	chr13:67124095..67126180-chr13:67127910..67129667,2	K562	blood:
18	chr13:66622814..66624893-chr13:66627297..66630041,2	K562	blood:
19	chr13:66500564..66501578-chr13:66540848..66541721,3	MCF-7	breast:
20	chr13:67109100..67110769-chr13:67114510..67116820,2	K562	blood:
21	chr13:67204110..67206444-chr13:67209007..67211337,2	K562	blood:
22	chr13:66500564..66501578-chr13:66540848..66541721,3	MCF-7	breast:
23	chr13:66978910..66981496-chr13:66983194..66984802,2	K562	blood:
24	chr13:67065181..67066891-chr13:67075366..67077021,2	MCF-7	breast:
25	chr13:66557440..66557967-chr13:82054818..82055319,2	MCF-7	breast:
26	chr13:66782802..66785217-chr13:66787154..66788780,2	MCF-7	breast:
27	chr10:29694023..29695542-chr13:67026635..67028155,2	MCF-7	breast:
28	chr13:66606276..66609107-chr13:66609295..66610970,2	MCF-7	breast:
29	chr13:67124095..67126180-chr13:67127910..67129667,2	K562	blood:
30	chr13:66423397..66425712-chr13:66435469..66437961,2	K562	blood:
31	chr13:66423397..66425712-chr13:66435469..66437961,2	K562	blood:
32	chr13:67118715..67120725-chr13:67121848..67124669,2	K562	blood:
33	chr13:66358245..66360880-chr16:71346372..71347872,2	MCF-7	breast:
34	chr13:66879908..66881972-chr13:66902872..66904425,2	K562	blood:
35	chr13:67090368..67092830-chr13:67094169..67095769,2	K562	blood:
36	chr13:66377468..66378968-chr8:43092929..43094908,2	MCF-7	breast:
37	chr13:67065287..67067165-chr13:67261665..67264552,2	MCF-7	breast:
38	chr13:66909684..66911530-chr13:66916300..66919201,2	K562	blood:
39	chr13:67118715..67120725-chr13:67121848..67124669,2	K562	blood:
40	chr13:66582815..66585533-chr13:66632919..66634778,2	K562	blood:
41	chr13:66677587..66680337-chr13:66682446..66685267,2	K562	blood:
42	chr13:66978910..66981496-chr13:66983194..66984802,2	K562	blood:
43	chr13:67130453..67132993-chr13:67135238..67136917,2	K562	blood:
44	chr13:67157975..67159957-chr13:67162075..67164465,2	K562	blood:
45	chr13:66355137..66357196-chr13:66362374..66364366,2	K562	blood:
46	chr13:67194212..67196284-chr13:67201796..67203435,2	MCF-7	breast:
47	chr13:66824109..66824810-chr16:71735977..71736631,2	MCF-7	breast:
48	chr13:66363582..66364363-chr21:32786060..32786817,2	MCF-7	breast:
49	chr12:28240626..28241152-chr13:66662383..66662898,2	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-AL445989.1-11	chr13:66569993-66570140	XLOC_010416
2	lnc-PCDH9-1	chr13:66805874-66806206	ENSG00000250631
3	lnc-PCDH9-6	chr13:66430425-66430559	NONHSAT034195
4	lnc-PCDH9-6	chr13:66410063-66410464	NONHSAT034195
5	lnc-AL445989.1-26	chr13:66846998-66847098	NONHSAT034208
6	lnc-AL445989.1-8	chr13:66449839-66449901	NONHSAT034197
7	lnc-AL445989.1-8	chr13:66451989-66452351	ENSG00000234767
8	lnc-AL445989.1-9	chr13:66510419-66510480	XLOC_010414
9	lnc-PCDH9-1	chr13:66718649-66718753	ENSG00000250631
10	lnc-AL445989.1-8	chr13:66451989-66452351	NONHSAT034197
11	lnc-AL445989.1-26	chr13:66843129-66844590	NONHSAT034207
12	lnc-AL445989.1-8	chr13:66440306-66440375	ENSG00000234767
13	lnc-AL445989.1-13	chr13:66878003-66878146	ENSG00000234527.1
14	lnc-AL445989.1-9	chr13:66503637-66503853	XLOC_010414
15	lnc-AL445989.1-8	chr13:66440195-66440400	NONHSAT034197
16	lnc-PCDH9-1	chr13:66715500-66715905	ENSG00000250631
17	lnc-AL445989.1-26	chr13:66851684-66852109	NONHSAT034208
18	lnc-AL445989.1-11	chr13:66628093-66628119	XLOC_010416
19	lnc-AL445989.1-10	chr13:66546596-66551943	XLOC_010415
20	lnc-AL445989.1-26	chr13:66844520-66844603	NONHSAT034208
21	lnc-AL445989.1-13	chr13:66897306-66897693	ENSG00000234527.1
22	lnc-AL445989.1-11	chr13:66569686-66569896	XLOC_010416
23	lnc-AL445989.1-10	chr13:66515195-66515334	XLOC_010415
24	lnc-AL445989.1-8	chr13:66449839-66449901	ENSG00000234767

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

(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	chr13:66877756-66877779
3	PCDH9	hsa-miR-155-5p	chr13:66878321-66878343

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: 19611 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:19611 , 50 per page) page: 1 2 3 4 5 6 7 ... 393

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530521347	chr13:66232317-66232318	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs535227154	chr13:66232319-66232320	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs553403068	chr13:66232384-66232385	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs576550832	chr13:66232426-66232427	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs375264247	chr13:66232427-66232428	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs192676242	chr13:66232437-66232438	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs548653509	chr13:66232451-66232452	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs555723639	chr13:66232463-66232464	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs576015156	chr13:66232470-66232471	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs149305560	chr13:66232489-66232490	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs184489422	chr13:66232515-66232516	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs368100478	chr13:66232565-66232566	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs190263348	chr13:66232597-66232598	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs181189975	chr13:66232614-66232615	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs564545527	chr13:66232806-66232807	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs565850637	chr13:66232844-66232845	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs533482818	chr13:66232864-66232865	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs550334273	chr13:66232899-66232900	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs569931117	chr13:66232906-66232907	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs186625198	chr13:66232909-66232910	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs549368119	chr13:66232966-66232967	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs368142948	chr13:66232976-66232977	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs144541436	chr13:66232983-66232984	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs189739057	chr13:66232984-66232985	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs180766877	chr13:66233003-66233004	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs185261314	chr13:66233012-66233013	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs571541183	chr13:66233064-66233065	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs60335340	chr13:66233082-66233083	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs539689974	chr13:66233089-66233090	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs539124032	chr13:66233151-66233152	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs148440552	chr13:66233156-66233157	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs575939700	chr13:66233236-66233237	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs142450912	chr13:66233244-66233245	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs145954582	chr13:66233245-66233246	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs190855939	chr13:66233264-66233265	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs183276147	chr13:66233295-66233296	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs9540505	chr13:66233325-66233326	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs577942936	chr13:66233358-66233359	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs543934334	chr13:66233392-66233393	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs375258277	chr13:66233393-66233394	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs139816620	chr13:66233405-66233406	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs543201547	chr13:66233429-66233430	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs367630575	chr13:66233478-66233479	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs186543751	chr13:66233483-66233484	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs80008063	chr13:66233521-66233522	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs191966042	chr13:66233644-66233645	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs182825104	chr13:66233650-66233651	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs112622660	chr13:66233690-66233691	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs571503815	chr13:66233726-66233727	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs79479840	chr13:66233737-66233738	Enhancers	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:1879 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:66231800-66232800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr13:66232000-66234000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr13:66232200-66232600	Enhancers	Adipose Nuclei	Adipose
4	chr13:66244200-66245000	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr13:66249600-66249800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr13:66251800-66252800	Enhancers	Osteobl	bone
7	chr13:66252000-66252400	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr13:66252000-66252400	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr13:66252000-66252400	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr13:66252000-66252600	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr13:66252000-66252600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr13:66252000-66252600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr13:66252200-66252600	Enhancers	Hela-S3	cervix
14	chr13:66252600-66253000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr13:66252800-66253200	Weak transcription	Osteobl	bone
16	chr13:66253000-66253600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr13:66253200-66253800	Enhancers	Osteobl	bone
18	chr13:66260600-66267000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
19	chr13:66263200-66267000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr13:66267000-66267200	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
21	chr13:66267000-66267600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr13:66267000-66267600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr13:66284600-66285200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr13:66298000-66298800	Enhancers	Dnd41	blood
25	chr13:66298200-66298600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr13:66298200-66298600	Enhancers	Fetal Stomach	stomach
27	chr13:66298200-66298800	Enhancers	Muscle Satellite Cultured Cells	--
28	chr13:66298200-66298800	Enhancers	Fetal Kidney	kidney
29	chr13:66298200-66298800	Enhancers	NHDF-Ad	bronchial
30	chr13:66298200-66299400	Enhancers	Fetal Lung	lung
31	chr13:66298200-66299800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr13:66298200-66300200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr13:66298800-66299200	Weak transcription	Fetal Kidney	kidney
34	chr13:66299200-66299800	Enhancers	Fetal Kidney	kidney
35	chr13:66299400-66299800	Enhancers	Fetal Heart	heart
36	chr13:66307000-66307600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr13:66318200-66319600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr13:66318400-66318800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr13:66318400-66319600	Enhancers	Osteobl	bone
40	chr13:66318800-66319000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr13:66318800-66319400	Enhancers	Adipose Nuclei	Adipose
42	chr13:66318800-66320600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr13:66319000-66319600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr13:66330600-66331400	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
45	chr13:66336600-66337200	Enhancers	Fetal Kidney	kidney
46	chr13:66342600-66343200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr13:66343000-66343400	Enhancers	H1 Cell Line	embryonic stem cell
48	chr13:66343000-66343400	Active TSS	iPS-20b Cell Line	embryonic stem cell
49	chr13:66347000-66347200	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr13:66347200-66349800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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