Variant report

Variant	nsv1037567
Chromosome Location	chr13:52643647-52802799
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3040)
CpG islands
(count:3300)
Chromatin interactive
region (count:58)
LncRNA
region (count:37)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:3040 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:52692261-52692519	K562	blood:	n/a	n/a
2	ARID3A	chr13:52701599-52702201	K562	blood:	n/a	n/a
3	ARID3A	chr13:52701870-52702197	HepG2	liver:	n/a	n/a
4	ARID3A	chr13:52703090-52703386	HepG2	liver:	n/a	n/a
5	ARID3A	chr13:52739173-52739424	HepG2	liver:	n/a	n/a
6	ARID3A	chr13:52768469-52768764	K562	blood:	n/a	n/a
7	ARID3A	chr13:52761418-52761903	K562	blood:	n/a	n/a
8	ARID3A	chr13:52735380-52735683	HepG2	liver:	n/a	chr13:52735628-52735644 chr13:52735627-52735643
9	ARID3A	chr13:52775549-52775803	HepG2	liver:	n/a	n/a
10	ARID3A	chr13:52736213-52737289	HepG2	liver:	n/a	n/a
11	ARID3A	chr13:52768441-52768762	HepG2	liver:	n/a	n/a
12	ARID3A	chr13:52645355-52645600	K562	blood:	n/a	n/a
13	ARID3A	chr13:52761673-52762111	HepG2	liver:	n/a	n/a
14	ARID3A	chr13:52678813-52679187	HepG2	liver:	n/a	n/a
15	ARID3A	chr13:52776095-52776205	HepG2	liver:	n/a	n/a
16	ATF1	chr13:52778134-52778252	K562	blood:	n/a	n/a
17	ATF1	chr13:52645130-52645616	K562	blood:	n/a	n/a
18	ATF1	chr13:52761531-52761864	K562	blood:	n/a	n/a
19	ATF2	chr13:52768359-52768829	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF2	chr13:52768366-52768847	GM12878	blood:	n/a	n/a
21	ATF2	chr13:52768357-52768861	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF2	chr13:52768333-52768885	GM12878	blood:	n/a	n/a
23	ATF3	chr13:52645090-52645562	K562	blood:	n/a	n/a
24	ATF3	chr13:52777990-52778282	K562	blood:	n/a	n/a
25	ATF3	chr13:52768340-52768838	A549	lung:	n/a	n/a
26	ATF3	chr13:52768417-52768760	A549	lung:	n/a	n/a
27	BACH1	chr13:52768461-52768767	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr13:52769515-52769849	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr13:52703283-52703494	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr13:52733037-52733825	H1-hESC	embryonic stem cell:	n/a	n/a
31	BATF	chr13:52797274-52797490	GM12878	blood:	n/a	n/a
32	BATF	chr13:52755736-52756031	GM12878	blood:	n/a	n/a
33	BATF	chr13:52768413-52768735	GM12878	blood:	n/a	n/a
34	BCL11A	chr13:52761551-52761791	GM12878	blood:	n/a	n/a
35	BCL11A	chr13:52761561-52761785	GM12878	blood:	n/a	n/a
36	BCL3	chr13:52768300-52768869	A549	lung:	n/a	n/a
37	BCL3	chr13:52768317-52768857	A549	lung:	n/a	n/a
38	BCL3	chr13:52648878-52649106	GM12878	blood:	n/a	n/a
39	BCL3	chr13:52765291-52765615	GM12878	blood:	n/a	n/a
40	BCLAF1	chr13:52768310-52768866	K562	blood:	n/a	n/a
41	BCLAF1	chr13:52732932-52733442	GM12878	blood:	n/a	n/a
42	BCLAF1	chr13:52769598-52769942	GM12878	blood:	n/a	chr13:52769765-52769778 chr13:52769770-52769783
43	BCLAF1	chr13:52768386-52768935	K562	blood:	n/a	n/a
44	BCLAF1	chr13:52768286-52768892	GM12878	blood:	n/a	n/a
45	BCLAF1	chr13:52768287-52768866	GM12878	blood:	n/a	n/a
46	BHLHE40	chr13:52701862-52702479	K562	blood:	n/a	n/a
47	BHLHE40	chr13:52703185-52703444	K562	blood:	n/a	n/a
48	BHLHE40	chr13:52768325-52769018	GM12878	blood:	n/a	n/a
49	BHLHE40	chr13:52733135-52733991	GM12878	blood:	n/a	n/a
50	BHLHE40	chr13:52645039-52645220	K562	blood:	n/a	n/a

(count:3300 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:52768659-52768709	NHDF-neo	bronchial:	n/a
2	chr13:52768717-52768767	Jurkat	blood:	n/a
3	chr13:52702856-52702906	PrEC	prostate:	n/a
4	chr13:52768669-52768719	K562	blood:	n/a
5	chr13:52703417-52703467	MCF10A-Er-Src	breast:	n/a
6	chr13:52703935-52703985	ovcar-3	ovarian:	n/a
7	chr13:52768659-52768709	NHDF-neo	bronchial:	n/a
8	chr13:52768717-52768767	Jurkat	blood:	n/a
9	chr13:52702856-52702906	PrEC	prostate:	n/a
10	chr13:52768669-52768719	K562	blood:	n/a
11	chr13:52703417-52703467	MCF10A-Er-Src	breast:	n/a
12	chr13:52703935-52703985	ovcar-3	ovarian:	n/a
13	chr13:52734018-52734068	ECC-1	luminal epithelium:	n/a
14	chr13:52769662-52769712	Caco-2	colon:	n/a
15	chr13:52699305-52699355	PFSK-1	brain:	n/a
16	chr13:52703160-52703210	PrEC	prostate:	n/a
17	chr13:52768717-52768767	PrEC	prostate:	n/a
18	chr13:52768717-52768767	HCT-116	colon:	n/a
19	chr13:52768659-52768709	LNCaP	prostate:	n/a
20	chr13:52702431-52702481	GM19239	blood:	n/a
21	chr13:52733860-52733910	HRCEpiC	kidney:	n/a
22	chr13:52769768-52769818	ProgFib	skin:	n/a
23	chr13:52703160-52703210	HCF	heart:	n/a
24	chr13:52703935-52703985	ECC-1	luminal epithelium:	n/a
25	chr13:52703368-52703418	AG04449	skin:	fetal
26	chr13:52701033-52701083	HRPEpiC	eye:	n/a
27	chr13:52768659-52768709	Caco-2	colon:	n/a
28	chr13:52702493-52702543	PANC-1	pancreas:	n/a
29	chr13:52733628-52733678	A549	lung:	n/a
30	chr13:52702856-52702906	Hela-S3	cervix:	n/a
31	chr13:52768659-52768709	A549	lung:	n/a
32	chr13:52707286-52707336	HAEpiC	amniotic membrane:	n/a
33	chr13:52768442-52768492	MCF10A-Er-Src	breast:	n/a
34	chr13:52768659-52768709	GM12878	blood:	n/a
35	chr13:52703368-52703418	HIPEpiC	eye:	n/a
36	chr13:52702856-52702906	HUVEC	blood vessel:	n/a
37	chr13:52768442-52768492	CMK	blood:	n/a
38	chr13:52769875-52769925	LNCaP	prostate:	n/a
39	chr13:52768680-52768730	HMEC	breast:	n/a
40	chr13:52734432-52734482	AG10803	skin:	n/a
41	chr13:52702460-52702510	HCF	heart:	n/a
42	chr13:52701588-52701638	CMK	blood:	n/a
43	chr13:52768669-52768719	H1-hESC	embryonic stem cell:	embryo
44	chr13:52733373-52733423	GM19239	blood:	n/a
45	chr13:52768539-52768589	HEK293	kidney:	embryo
46	chr13:52768717-52768767	SK-N-SH_RA	brain:	n/a
47	chr13:52733860-52733910	SAEC	small airway:	n/a
48	chr13:52766123-52766173	AoSMC	blood vessel:	n/a
49	chr13:52703373-52703423	ovcar-3	ovarian:	n/a
50	chr13:52768669-52768719	HNPCEpiC	eye:	n/a

(count:58 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr13:52687652..52690053-chr13:52690967..52693766,2	K562	blood:
2	chr13:52600318..52601043-chr13:52701669..52702499,2	MCF-7	breast:
3	chr13:52718895..52720527-chr13:52725427..52728131,2	MCF-7	breast:
4	chr13:52675167..52677074-chr13:52681306..52682883,2	K562	blood:
5	chr13:52584477..52586943-chr13:52701489..52703372,3	K562	blood:
6	chr13:52729535..52732308-chr13:52732328..52734703,4	K562	blood:
7	chr13:52675167..52677074-chr13:52681306..52682883,2	K562	blood:
8	chr13:52682568..52684344-chr13:52687301..52689762,2	K562	blood:
9	chr13:52584477..52586900-chr13:52700506..52703372,3	K562	blood:
10	chr13:52683996..52685764-chr13:52687463..52689189,2	K562	blood:
11	chr13:52691024..52693567-chr13:52694230..52696395,3	K562	blood:
12	chr13:52509591..52510539-chr13:52701676..52702543,4	MCF-7	breast:
13	chr13:52025014..52028193-chr13:52674077..52677651,3	K562	blood:
14	chr13:52687652..52690053-chr13:52690967..52693766,2	K562	blood:
15	chr13:52714165..52716732-chr13:52726469..52728185,2	MCF-7	breast:
16	chr13:52377651..52379551-chr13:52768569..52770283,3	MCF-7	breast:
17	chr13:52026008..52028349-chr13:52675344..52677651,2	K562	blood:
18	chr13:52735080..52737033-chr13:52768484..52770040,2	MCF-7	breast:
19	chr13:52725842..52728742-chr13:52731896..52733455,2	MCF-7	breast:
20	chr13:52762333..52764289-chr13:52768534..52770234,2	MCF-7	breast:
21	chr13:52714165..52716732-chr13:52726469..52728185,2	MCF-7	breast:
22	chr13:52388965..52389862-chr13:52701684..52702477,3	K562	blood:
23	chr13:52682568..52684344-chr13:52687301..52689762,2	K562	blood:
24	chr13:52768239..52768779-chr21:34775626..34776496,2	NB4	blood:
25	chr13:52768256..52771397-chr13:52784460..52787312,3	MCF-7	breast:
26	chr13:52699126..52701652-chr13:52702989..52705135,2	K562	blood:
27	chr13:52691024..52693567-chr13:52694230..52696395,3	K562	blood:
28	chr13:52718895..52720527-chr13:52725427..52728131,2	MCF-7	breast:
29	chr13:52680463..52681985-chr13:52686130..52688988,2	K562	blood:
30	chr13:52683996..52685764-chr13:52687463..52689189,2	K562	blood:
31	chr13:52699126..52701652-chr13:52702989..52705135,2	K562	blood:
32	chr13:52377591..52379548-chr13:52768375..52770242,2	K562	blood:
33	chr13:52522795..52524482-chr13:52694291..52697001,2	K562	blood:
34	chr13:52730788..52732496-chr13:52768343..52769860,2	MCF-7	breast:
35	chr13:52726747..52729442-chr13:52731857..52734601,2	K562	blood:
36	chr1:45194788..45196878-chr13:52740302..52742412,2	MCF-7	breast:
37	chr13:52377335..52378174-chr13:52702786..52703324,2	K562	blood:
38	chr13:52728953..52731151-chr13:52731981..52733789,2	MCF-7	breast:
39	chr13:52701771..52705558-chr13:52767896..52769871,3	MCF-7	breast:
40	chr13:52376169..52378547-chr13:52701514..52703656,2	MCF-7	breast:
41	chr13:52645505..52647526-chr13:52648523..52650064,2	K562	blood:
42	chr13:52768173..52768983-chr13:53191222..53192131,3	NB4	blood:
43	chr13:52469831..52471115-chr13:52701846..52702769,5	MCF-7	breast:
44	chr13:52725842..52728742-chr13:52731896..52733455,2	MCF-7	breast:
45	chr13:52486050..52486951-chr13:52701619..52702125,2	MCF-7	breast:
46	chr13:52729535..52732308-chr13:52732328..52734703,4	K562	blood:
47	chr13:52578352..52579378-chr13:52701728..52702446,3	MCF-7	breast:
48	chr13:52701771..52705558-chr13:52767896..52769871,3	MCF-7	breast:
49	chr13:52733390..52734978-chr13:52735915..52738886,2	K562	blood:
50	chr13:52680463..52681985-chr13:52686130..52688988,2	K562	blood:

(count:37 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NEK3-1	chr13:52768389-52768581	NONHSAT033970
2	lnc-NEK3-1	chr13:52745293-52745383	NONHSAT033972
3	lnc-NEK3-1	chr13:52754717-52754789	NONHSAT033972
4	lnc-UTP14C-1	chr13:52703027-52706193	NONHSAT033962
5	lnc-NEK3-1	chr13:52768293-52768581	NONHSAT033975
6	lnc-NEK3-1	chr13:52749774-52749911	NONHSAT033972
7	lnc-UTP14C-1	chr13:52703031-52706193	NR_110306
8	lnc-NEK3-1	chr13:52768389-52768582	NONHSAT033973
9	lnc-NEK3-1	chr13:52763774-52764051	NONHSAT033970
10	lnc-NEK3-1	chr13:52763774-52764049	NONHSAT033975
11	lnc-NEK3-1	chr13:52763774-52764049	NONHSAT033976
12	lnc-NEK3-1	chr13:52760818-52760958	NONHSAT033976
13	lnc-NEK3-1	chr13:52754717-52754789	NONHSAT033970
14	lnc-NEK3-1	chr13:52760818-52760958	NONHSAT033975
15	lnc-NEK3-1	chr13:52745293-52745385	NONHSAT033970
16	lnc-NEK3-1	chr13:52744193-52744234	NONHSAT033973
17	lnc-NEK3-1	chr13:52749774-52749911	NONHSAT033970
18	lnc-NEK3-1	chr13:52760818-52760958	NONHSAT033972
19	lnc-NEK3-1	chr13:52768389-52768582	NONHSAT033972
20	lnc-NEK3-1	chr13:52745293-52745383	NONHSAT033973
21	lnc-NEK3-1	chr13:52744122-52744224	NONHSAT033970
22	lnc-NEK3-1	chr13:52749774-52749911	NONHSAT033973
23	lnc-NEK3-1	chr13:52763774-52764049	NONHSAT033972
24	lnc-NEK3-1	chr13:52766939-52768570	NONHSAT033977
25	lnc-NEK3-1	chr13:52760878-52760958	NONHSAT033970
26	lnc-NEK3-1	chr13:52760818-52760958	NONHSAT033973
27	lnc-NEK3-1	chr13:52758111-52758249	NONHSAT033970
28	lnc-NEK3-1	chr13:52743125-52743441	NONHSAT033970
29	lnc-NEK3-1	chr13:52758111-52758249	NONHSAT033973
30	lnc-UTP14C-1	chr13:52706594-52706859	NONHSAT033962
31	lnc-NEK3-1	chr13:52768394-52768598	NONHSAT033976
32	lnc-NEK3-1	chr13:52758138-52758249	NONHSAT033976
33	lnc-NEK3-1	chr13:52758111-52758249	NONHSAT033972
34	lnc-UTP14C-1	chr13:52706594-52706859	NR_110306
35	lnc-NEK3-1	chr13:52754717-52754789	NONHSAT033973
36	lnc-NEK3-1	chr13:52758118-52758249	NONHSAT033975
37	lnc-NEK3-1	chr13:52744107-52744191	NONHSAT033972

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	NEK3	hsa-miR-98-5p	chr13:52706917-52706910
2	NEK3	hsa-miR-98-5p	chr13:52706911-52706932

Variant related genes	Relation type
NEK5	TF binding region
NEK3	TF binding region
MRPS31P5	TF binding region
NEK5	CpG island
NEK3	CpG island
MRPS31P5	CpG island
ENSG00000102796	chromatin interactions
ENSG00000231856	chromatin interactions
ENSG00000224892	chromatin interactions
ENSG00000197168	chromatin interactions
ENSG00000102786	chromatin interactions
ENSG00000139675	chromatin interactions
ENSG00000236778	chromatin interactions
ENSG00000243406	chromatin interactions
ENSG00000250299	chromatin interactions
ENSG00000159128	chromatin interactions
ENSG00000200169	chromatin interactions
ENSG00000136098	chromatin interactions
ENSG00000253710	chromatin interactions
ENSG00000123191	chromatin interactions

Extended variants
information (count: 4919 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:4919 , 50 per page) page: 1 2 3 4 5 6 7 ... 99

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566611949	chr13:52643669-52643670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs182351156	chr13:52643701-52643702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs576323606	chr13:52643733-52643734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs566189061	chr13:52643742-52643743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs545406953	chr13:52643744-52643745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs558936676	chr13:52643749-52643750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs9535851	chr13:52643757-52643758	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs140384464	chr13:52643775-52643776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs375758730	chr13:52643803-52643804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs148006088	chr13:52643809-52643810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs528942139	chr13:52643823-52643824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs542325358	chr13:52643858-52643859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs562626881	chr13:52643890-52643891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs531164935	chr13:52643949-52643950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs376112981	chr13:52644001-52644002	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs368647872	chr13:52644002-52644003	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs575789568	chr13:52644005-52644006	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs186635816	chr13:52644022-52644023	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs576970017	chr13:52644028-52644029	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs144175762	chr13:52644029-52644030	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs146519068	chr13:52644073-52644074	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs536466111	chr13:52644142-52644143	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs34126896	chr13:52644297-52644298	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs549979012	chr13:52644355-52644356	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs140957261	chr13:52644362-52644363	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs538613274	chr13:52644399-52644400	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs35172666	chr13:52644464-52644465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs71088010	chr13:52644471-52644472	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs398022814	chr13:52644473-52644474	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs558949402	chr13:52644493-52644494	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs552387176	chr13:52644521-52644522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs572400435	chr13:52644527-52644528	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs545881316	chr13:52644627-52644628	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs554860670	chr13:52644670-52644671	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs190257855	chr13:52644748-52644749	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs544001272	chr13:52644750-52644751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs562404414	chr13:52644776-52644777	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs576129221	chr13:52644858-52644859	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs544676401	chr13:52644951-52644952	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs112338664	chr13:52645063-52645064	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs369061176	chr13:52645067-52645068	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs527567133	chr13:52645088-52645089	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs537775599	chr13:52645118-52645119	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs547679618	chr13:52645154-52645155	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs561187557	chr13:52645167-52645168	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs182838563	chr13:52645238-52645239	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs112112821	chr13:52645275-52645276	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs79471741	chr13:52645281-52645282	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
49	rs150145876	chr13:52645304-52645305	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs539167790	chr13:52645313-52645314	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:110)

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
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	16774939	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	19242612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	17245344	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Multiple myeloma	19135901	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Prostate cancer	16461572	CNVD
Merkel cell carcinoma	19020549	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21858162	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	17237825	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Gastric cancer	17908304	CNVD
Breast cancer	18852474	CNVD
Myelofibrosis	22110671	CNVD
craniofacial dysmorphism	21918468	CNVD
Glioblastoma multiforme	22286061	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
Breast cancer	22522925	CNVD

Chromatin state (count:3444 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:52641800-52645000	Weak transcription	Fetal Heart	heart
2	chr13:52644000-52644400	ZNF genes & repeats	Brain Anterior Caudate	brain
3	chr13:52644200-52646000	Enhancers	HSMMtube	muscle
4	chr13:52644400-52647800	Weak transcription	Brain Anterior Caudate	brain
5	chr13:52644600-52646000	Enhancers	HSMM	muscle
6	chr13:52644800-52646200	Enhancers	HepG2	liver
7	chr13:52644800-52646200	Enhancers	K562	blood
8	chr13:52645000-52645800	Enhancers	Muscle Satellite Cultured Cells	--
9	chr13:52645000-52646000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr13:52645000-52646000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr13:52645000-52646000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr13:52645000-52646000	Enhancers	HMEC	breast
13	chr13:52645200-52645800	Enhancers	Dnd41	blood
14	chr13:52645200-52645800	Enhancers	NHEK	skin
15	chr13:52645400-52645800	Enhancers	HUVEC	blood vessel
16	chr13:52645400-52646000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr13:52645400-52647000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
18	chr13:52645600-52646000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr13:52655000-52655600	Enhancers	HepG2	liver
20	chr13:52656800-52658000	Weak transcription	Lung	lung
21	chr13:52658000-52658200	Enhancers	Lung	lung
22	chr13:52658400-52660400	Enhancers	Stomach Mucosa	stomach
23	chr13:52658800-52659200	Enhancers	Fetal Brain Male	brain
24	chr13:52659200-52660000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr13:52659200-52660200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr13:52659200-52660200	Enhancers	HSMM	muscle
27	chr13:52659200-52660400	Enhancers	HSMMtube	muscle
28	chr13:52659400-52660000	Enhancers	Muscle Satellite Cultured Cells	--
29	chr13:52659400-52660200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr13:52659600-52660000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr13:52659600-52660000	Enhancers	NHEK	skin
32	chr13:52659600-52660200	Enhancers	HMEC	breast
33	chr13:52660200-52661400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr13:52661200-52663800	Enhancers	HepG2	liver
35	chr13:52661400-52663600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr13:52661800-52662400	Enhancers	Liver	Liver
37	chr13:52661800-52662400	Enhancers	Placenta	Placenta
38	chr13:52662200-52662400	Enhancers	Stomach Mucosa	stomach
39	chr13:52663400-52663800	Enhancers	Adipose Nuclei	Adipose
40	chr13:52664000-52664800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr13:52670800-52672200	Enhancers	HepG2	liver
42	chr13:52671000-52671600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr13:52671400-52671600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr13:52671400-52671800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr13:52671600-52672400	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr13:52671800-52672400	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr13:52672200-52672400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr13:52672200-52677600	Weak transcription	HepG2	liver
49	chr13:52677600-52680000	Enhancers	HepG2	liver
50	chr13:52679600-52680200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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