Variant report

Variant	nsv915828
Chromosome Location	chr13:66544825-67212201
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2606)
CpG islands
(count:915)
Chromatin interactive
region (count:48)
LncRNA
region (count:13)
Mature miRNA
region (count: 2)
miRNA target
sites (count:3)

(count:2606 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

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	chr13:66643768-66644097	K562	blood:	n/a	n/a
3	ARID3A	chr13:66713473-66713809	HepG2	liver:	n/a	n/a
4	ARID3A	chr13:66886857-66887028	HepG2	liver:	n/a	n/a
5	ARID3A	chr13:67142089-67142310	K562	blood:	n/a	n/a
6	ARID3A	chr13:66648258-66648447	K562	blood:	n/a	n/a
7	ARID3A	chr13:66651230-66651680	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	chr13:67024589-67024601	K562	blood:	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	chr13:66643737-66644023	K562	blood:	n/a	n/a
14	ATF1	chr13:66650593-66650896	K562	blood:	n/a	n/a
15	ATF1	chr13:66999986-67000196	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	chr13:66712420-66712936	GM12878	blood:	n/a	n/a
22	BATF	chr13:67052441-67052616	GM12878	blood:	n/a	n/a
23	BATF	chr13:66702801-66703238	GM12878	blood:	n/a	n/a
24	BATF	chr13:67081195-67081436	GM12878	blood:	n/a	n/a
25	BATF	chr13:66712465-66712951	GM12878	blood:	n/a	n/a
26	BCL11A	chr13:66798756-66799093	H1-hESC	embryonic stem cell:	n/a	n/a
27	BCL11A	chr13:66712423-66713013	GM12878	blood:	n/a	chr13:66712844-66712853
28	BCL11A	chr13:66712457-66712949	GM12878	blood:	n/a	chr13:66712844-66712853
29	BCL11A	chr13:66702875-66703088	GM12878	blood:	n/a	n/a
30	BCL11A	chr13:66798709-66799125	H1-hESC	embryonic stem cell:	n/a	n/a
31	BCL11A	chr13:67159926-67160259	GM12878	blood:	n/a	n/a
32	BCL11A	chr13:66702751-66703109	GM12878	blood:	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	chr13:66648396-66648557	K562	blood:	n/a	n/a
37	BHLHE40	chr13:66712457-66712998	GM12878	blood:	n/a	n/a
38	BHLHE40	chr13:66739043-66739104	K562	blood:	n/a	n/a
39	BHLHE40	chr13:66902776-66902779	K562	blood:	n/a	n/a
40	BHLHE40	chr13:66917482-66917943	K562	blood:	n/a	n/a
41	BRCA1	chr13:67088395-67088424	H1-hESC	embryonic stem cell:	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	CBX3	chr13:66784811-66785347	HCT-116	colon:	n/a	n/a
45	CBX3	chr13:66861033-66861253	K562	blood:	n/a	n/a
46	CBX3	chr13:66643667-66644035	K562	blood:	n/a	n/a
47	CBX3	chr13:67137257-67137558	K562	blood:	n/a	n/a
48	CBX3	chr13:66784784-66785224	HCT-116	colon:	n/a	n/a
49	CCNT2	chr13:66617039-66617239	K562	blood:	n/a	n/a
50	CCNT2	chr13:66589547-66589747	K562	blood:	n/a	n/a

(count:915 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:66981290-66981340	HCT-116	colon:	n/a
2	chr13:66583686-66583736	RPTEC	kidney:	n/a
3	chr13:67155091-67155141	HIPEpiC	eye:	n/a
4	chr13:67196386-67196436	SK-N-MC	brain:	n/a
5	chr13:66919912-66919962	U87	brain:	n/a
6	chr13:66583583-66583633	T-47D	breast:	n/a
7	chr13:67101887-67101937	BE2_C	brain:	n/a
8	chr13:66878738-66878788	GM19239	blood:	n/a
9	chr13:66983730-66983780	BE2_C	brain:	n/a
10	chr13:66983676-66983726	Jurkat	blood:	n/a
11	chr13:66983730-66983780	NB4	blood:	n/a
12	chr13:66981290-66981340	H1-hESC	embryonic stem cell:	embryo
13	chr13:67101887-67101937	HNPCEpiC	eye:	n/a
14	chr13:66878738-66878788	LNCaP	prostate:	n/a
15	chr13:67196386-67196436	HNPCEpiC	eye:	n/a
16	chr13:67101887-67101937	AG04449	skin:	fetal
17	chr13:66878738-66878788	BE2_C	brain:	n/a
18	chr13:66983676-66983726	GM12892	blood:	n/a
19	chr13:67101887-67101937	HMEC	breast:	n/a
20	chr13:67197133-67197183	SK-N-MC	brain:	n/a
21	chr13:66983730-66983780	CMK	blood:	n/a
22	chr13:67197277-67197327	U87	brain:	n/a
23	chr13:67197277-67197327	AG04449	skin:	fetal
24	chr13:67155091-67155141	NB4	blood:	n/a
25	chr13:66983676-66983726	SK-N-SH	brain:	n/a
26	chr13:66607275-66607325	ovcar-3	ovarian:	n/a
27	chr13:66983676-66983726	HMEC	breast:	n/a
28	chr13:66607275-66607325	SK-N-SH_RA	brain:	n/a
29	chr13:66919912-66919962	NB4	blood:	n/a
30	chr13:67197277-67197327	A549	lung:	n/a
31	chr13:67197277-67197327	MCF-7	breast:	n/a
32	chr13:66983676-66983726	HRCEpiC	kidney:	n/a
33	chr13:66878738-66878788	CMK	blood:	n/a
34	chr13:67101887-67101937	HCF	heart:	n/a
35	chr13:66919912-66919962	HPAEpiC	pulmonary alveolar:	n/a
36	chr13:66583583-66583633	AoSMC	blood vessel:	n/a
37	chr13:67197277-67197327	GM12878	blood:	n/a
38	chr13:66583686-66583736	SAEC	small airway:	n/a
39	chr13:66878738-66878788	Hepatocyte	liver:	n/a
40	chr13:66983730-66983780	IMR90	lung:	fetal
41	chr13:66929165-66929215	HAEpiC	amniotic membrane:	n/a
42	chr13:67197133-67197183	K562	blood:	n/a
43	chr13:66607275-66607325	SK-N-SH	brain:	n/a
44	chr13:67197277-67197327	ProgFib	skin:	n/a
45	chr13:66583583-66583633	HRCEpiC	kidney:	n/a
46	chr13:66929165-66929215	AG04449	skin:	fetal
47	chr13:66983676-66983726	HCM	heart:	n/a
48	chr13:66583686-66583736	HPAEpiC	pulmonary alveolar:	n/a
49	chr13:67197173-67197223	HNPCEpiC	eye:	n/a
50	chr13:67197173-67197223	AoSMC	blood vessel:	n/a

(count:48 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:67204110..67206444-chr13:67209007..67211337,2	K562	blood:
2	chr13:67194212..67196284-chr13:67201796..67203435,2	MCF-7	breast:
3	chr13:66918574..66921439-chr13:66945401..66948264,2	MCF-7	breast:
4	chr13:66978910..66981496-chr13:66983194..66984802,2	K562	blood:
5	chr13:66824109..66824810-chr16:71735977..71736631,2	MCF-7	breast:
6	chr13:67118715..67120725-chr13:67121848..67124669,2	K562	blood:
7	chr12:28240626..28241152-chr13:66662383..66662898,2	MCF-7	breast:
8	chr13:67090368..67092830-chr13:67094169..67095769,2	K562	blood:
9	chr13:66606276..66609107-chr13:66609295..66610970,2	MCF-7	breast:
10	chr13:66978910..66981496-chr13:66983194..66984802,2	K562	blood:
11	chr13:66557440..66557967-chr13:82054818..82055319,2	MCF-7	breast:
12	chr13:66879908..66881972-chr13:66902872..66904425,2	K562	blood:
13	chr13:67109100..67110769-chr13:67114510..67116820,2	K562	blood:
14	chr13:67130453..67132993-chr13:67135238..67136917,2	K562	blood:
15	chr13:67090368..67092830-chr13:67094169..67095769,2	K562	blood:
16	chr13:66582815..66585533-chr13:66632919..66634778,2	K562	blood:
17	chr13:67130437..67132993-chr13:67135417..67138774,3	K562	blood:
18	chr13:67124095..67126180-chr13:67127910..67129667,2	K562	blood:
19	chr13:66622814..66624893-chr13:66627297..66630041,2	K562	blood:
20	chr13:67109100..67110769-chr13:67114510..67116820,2	K562	blood:
21	chr13:66677587..66680337-chr13:66682446..66685267,2	K562	blood:
22	chr13:66901663..66903255-chr13:66906195..66907818,2	K562	blood:
23	chr13:67065181..67066891-chr13:67075366..67077021,2	MCF-7	breast:
24	chr10:29694023..29695542-chr13:67026635..67028155,2	MCF-7	breast:
25	chr13:66901663..66903255-chr13:66906195..66907818,2	K562	blood:
26	chr13:67065181..67066891-chr13:67075366..67077021,2	MCF-7	breast:
27	chr13:66622814..66624893-chr13:66627297..66630041,2	K562	blood:
28	chr13:66725373..66727381-chr13:66728791..66730521,2	K562	blood:
29	chr13:67124095..67126180-chr13:67127910..67129667,2	K562	blood:
30	chr13:66918574..66921439-chr13:66945401..66948264,2	MCF-7	breast:
31	chr13:67157975..67159957-chr13:67162075..67164465,2	K562	blood:
32	chr13:67066396..67067204-chr13:67263202..67263856,3	MCF-7	breast:
33	chr13:66909684..66911530-chr13:66916300..66919201,2	K562	blood:
34	chr13:66879908..66881972-chr13:66902872..66904425,2	K562	blood:
35	chr13:67065287..67067165-chr13:67261665..67264552,2	MCF-7	breast:
36	chr13:66677587..66680337-chr13:66682446..66685267,2	K562	blood:
37	chr13:67194212..67196284-chr13:67201796..67203435,2	MCF-7	breast:
38	chr13:66725373..66727381-chr13:66728791..66730521,2	K562	blood:
39	chr13:66606276..66609107-chr13:66609295..66610970,2	MCF-7	breast:
40	chr13:66782802..66785217-chr13:66787154..66788780,2	MCF-7	breast:
41	chr13:67027655..67028155-chr8:43092779..43093429,2	MCF-7	breast:
42	chr13:66582815..66585533-chr13:66632919..66634778,2	K562	blood:
43	chr13:67130437..67132993-chr13:67135417..67138774,3	K562	blood:
44	chr13:66782802..66785217-chr13:66787154..66788780,2	MCF-7	breast:
45	chr13:67157975..67159957-chr13:67162075..67164465,2	K562	blood:
46	chr13:67118715..67120725-chr13:67121848..67124669,2	K562	blood:
47	chr13:67130453..67132993-chr13:67135238..67136917,2	K562	blood:
48	chr13:66909684..66911530-chr13:66916300..66919201,2	K562	blood:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL445989.1-10	chr13:66546596-66551943	XLOC_010415
2	lnc-AL445989.1-11	chr13:66569993-66570140	XLOC_010416
3	lnc-AL445989.1-13	chr13:66878003-66878146	ENSG00000234527.1
4	lnc-AL445989.1-26	chr13:66843129-66844590	NONHSAT034207
5	lnc-AL445989.1-26	chr13:66851684-66852109	NONHSAT034208
6	lnc-AL445989.1-26	chr13:66844520-66844603	NONHSAT034208
7	lnc-AL445989.1-11	chr13:66569686-66569896	XLOC_010416
8	lnc-AL445989.1-11	chr13:66628093-66628119	XLOC_010416
9	lnc-PCDH9-1	chr13:66718649-66718753	ENSG00000250631
10	lnc-AL445989.1-13	chr13:66897306-66897693	ENSG00000234527.1
11	lnc-PCDH9-1	chr13:66805874-66806206	ENSG00000250631
12	lnc-PCDH9-1	chr13:66715500-66715905	ENSG00000250631
13	lnc-AL445989.1-26	chr13:66846998-66847098	NONHSAT034208

miRNA name	Chromosome Location	mirBase accession
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	chr13:66877756-66877779
2	PCDH9	hsa-miR-155-5p	chr13:66878321-66878343
3	PCDH9	hsa-miR-155-5p	chr13:66878327-66878320

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

Extended variants
information (count: 13857 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:13857 , 50 per page) page: 1 2 3 4 5 6 7 ... 278

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs528674208	chr13:66545023-66545024	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs561536906	chr13:66545035-66545036	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs551528880	chr13:66545075-66545076	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs60541953	chr13:66545082-66545083	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs540911688	chr13:66545174-66545175	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs117037718	chr13:66545191-66545192	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs147318650	chr13:66545211-66545212	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs375206874	chr13:66545240-66545241	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs58920081	chr13:66545253-66545254	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs182495418	chr13:66545338-66545339	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs376340585	chr13:66545367-66545368	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs536179052	chr13:66545369-66545370	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs549276456	chr13:66545377-66545378	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs565951990	chr13:66545437-66545438	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs373952075	chr13:66545458-66545459	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs187199672	chr13:66545601-66545602	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs570011546	chr13:66545605-66545606	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs568535171	chr13:66545607-66545608	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs191280737	chr13:66545648-66545649	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs1146804	chr13:66545669-66545670	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs537588580	chr13:66545715-66545716	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs71442682	chr13:66545746-66545747	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs144159358	chr13:66545752-66545753	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs75152715	chr13:66545790-66545791	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs147773119	chr13:66545839-66545840	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs78151313	chr13:66545846-66545847	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs573151878	chr13:66545849-66545850	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs370076871	chr13:66545853-66545854	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs77905801	chr13:66545856-66545857	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs71442683	chr13:66545863-66545864	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs374388596	chr13:66545917-66545918	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs549885366	chr13:66545932-66545933	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs61956689	chr13:66545953-66545954	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs183712721	chr13:66545994-66545995	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs149079353	chr13:66546456-66546457	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs528070554	chr13:66546534-66546535	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs367598562	chr13:66546552-66546553	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs66943444	chr13:66546558-66546559	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs61429957	chr13:66546559-66546560	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs144796336	chr13:66546627-66546628	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
41	rs371589114	chr13:66546716-66546717	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
42	rs540948539	chr13:66546723-66546724	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
43	rs146744923	chr13:66546730-66546731	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
44	rs181576308	chr13:66546790-66546791	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
45	rs55726105	chr13:66546825-66546826	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
46	rs56104294	chr13:66546865-66546866	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
47	rs185337792	chr13:66546954-66546955	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
48	rs11839567	chr13:66546958-66546959	Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs188633928	chr13:66546966-66546967	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
50	rs181281372	chr13:66546967-66546968	Enhancers	lncRNA	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
Schizophrenia	20967226	CNVD
Bipolar disorder	19114987	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:1523 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:66545000-66545600	Enhancers	iPS-20b Cell Line	embryonic stem cell
2	chr13:66545000-66546000	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr13:66545000-66546000	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr13:66545000-66546000	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr13:66545200-66546000	Enhancers	H1 Cell Line	embryonic stem cell
6	chr13:66545400-66545800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr13:66545400-66546000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr13:66545400-66546000	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr13:66545600-66546000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr13:66546400-66547000	Enhancers	Aorta	Aorta
11	chr13:66551800-66552000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr13:66559600-66559800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr13:66562400-66562600	Enhancers	Left Ventricle	heart
14	chr13:66566400-66566800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr13:66575000-66575600	Enhancers	Pancreatic Islets	Pancreatic Islet
16	chr13:66575200-66575600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr13:66584800-66587400	Active TSS	K562	blood
18	chr13:66605800-66608600	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr13:66605800-66608600	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr13:66605800-66608600	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr13:66606200-66606600	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr13:66606400-66607600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr13:66606600-66607800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chr13:66607800-66608000	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr13:66607800-66608400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr13:66607800-66608600	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr13:66608000-66608400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr13:66608400-66610400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr13:66608600-66610000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
30	chr13:66608600-66610200	Weak transcription	HUES64 Cell Line	embryonic stem cell
31	chr13:66610000-66610200	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr13:66610000-66610800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
33	chr13:66610200-66610600	Enhancers	Brain Germinal Matrix	brain
34	chr13:66610200-66610800	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr13:66610200-66611600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr13:66610400-66610600	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr13:66610400-66611000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr13:66613000-66613400	Enhancers	K562	blood
39	chr13:66613000-66613800	Enhancers	Pancreas	Pancrea
40	chr13:66618000-66620800	Weak transcription	Fetal Brain Male	brain
41	chr13:66619000-66620000	Enhancers	Liver	Liver
42	chr13:66619800-66620600	Enhancers	Breast Myoepithelial Primary Cells	Breast
43	chr13:66626800-66627400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr13:66634200-66635000	Bivalent Enhancer	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr13:66634400-66634600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr13:66634600-66636400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr13:66636400-66636600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr13:66636600-66638800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr13:66643200-66644000	Enhancers	Liver	Liver
50	chr13:66643600-66644200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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