Variant report

Variant	nsv430560
Chromosome Location	chr13:49930643-50059354
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1570)
CpG islands
(count:1709)
Chromatin interactive
region (count:70)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1570 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:50040074-50041075	HepG2	liver:	n/a	n/a
2	ARID3A	chr13:49995639-49995842	HepG2	liver:	n/a	n/a
3	ARID3A	chr13:50018043-50018342	K562	blood:	n/a	n/a
4	ARID3A	chr13:50018824-50019531	K562	blood:	n/a	n/a
5	ARID3A	chr13:50017884-50018589	HepG2	liver:	n/a	n/a
6	ARID3A	chr13:50022201-50022473	K562	blood:	n/a	n/a
7	ARID3A	chr13:50038795-50039574	HepG2	liver:	n/a	n/a
8	ATF1	chr13:49948735-49949011	K562	blood:	n/a	n/a
9	ATF2	chr13:50017722-50018650	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr13:50028627-50029260	GM12878	blood:	n/a	n/a
11	ATF2	chr13:50028547-50029303	GM12878	blood:	n/a	n/a
12	ATF2	chr13:50017799-50018696	GM12878	blood:	n/a	n/a
13	ATF2	chr13:50017524-50018660	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr13:50017921-50018315	GM12878	blood:	n/a	n/a
15	BACH1	chr13:49974206-49974216	K562	blood:	n/a	n/a
16	BATF	chr13:50033735-50034011	GM12878	blood:	n/a	n/a
17	BATF	chr13:50028580-50029122	GM12878	blood:	n/a	n/a
18	BATF	chr13:50028595-50029091	GM12878	blood:	n/a	n/a
19	BATF	chr13:50033761-50033980	GM12878	blood:	n/a	n/a
20	BCLAF1	chr13:50017854-50018762	GM12878	blood:	n/a	chr13:50018730-50018743
21	BCLAF1	chr13:50017479-50018901	GM12878	blood:	n/a	chr13:50018730-50018743
22	BHLHE40	chr13:50019165-50019509	A549	lung:	n/a	n/a
23	BHLHE40	chr13:50040050-50040053	HepG2	liver:	n/a	n/a
24	BHLHE40	chr13:50017572-50017700	HepG2	liver:	n/a	n/a
25	BHLHE40	chr13:50019167-50019537	HepG2	liver:	n/a	n/a
26	BHLHE40	chr13:50017924-50019861	GM12878	blood:	n/a	n/a
27	BHLHE40	chr13:50017907-50019581	K562	blood:	n/a	n/a
28	BHLHE40	chr13:50028754-50029257	GM12878	blood:	n/a	n/a
29	BHLHE40	chr13:49995589-49995906	HepG2	liver:	n/a	n/a
30	BHLHE40	chr13:49984789-49984955	GM12878	blood:	n/a	n/a
31	BHLHE40	chr13:49946064-49946407	HepG2	liver:	n/a	n/a
32	BRCA1	chr13:50017958-50018595	HepG2	liver:	n/a	n/a
33	BRCA1	chr13:50017752-50018443	H1-hESC	embryonic stem cell:	n/a	n/a
34	BRCA1	chr13:50017808-50018576	GM12878	blood:	n/a	n/a
35	BRCA1	chr13:49948748-49949109	Hela-S3	cervix:	n/a	chr13:49949075-49949082
36	BRCA1	chr13:50017797-50019617	Hela-S3	cervix:	n/a	n/a
37	CBX3	chr13:50017976-50018310	K562	blood:	n/a	n/a
38	CBX3	chr13:50037375-50037753	HCT-116	colon:	n/a	n/a
39	CBX3	chr13:50037420-50037685	K562	blood:	n/a	n/a
40	CBX3	chr13:49978764-49979124	K562	blood:	n/a	n/a
41	CBX3	chr13:49978763-49979094	K562	blood:	n/a	n/a
42	CBX3	chr13:50037345-50037712	K562	blood:	n/a	n/a
43	CBX3	chr13:50017739-50018627	K562	blood:	n/a	n/a
44	CCNT2	chr13:50018091-50019133	K562	blood:	n/a	chr13:50018752-50018761
45	CEBPB	chr13:50017986-50018199	HepG2	liver:	n/a	n/a
46	CEBPB	chr13:49946236-49946288	K562	blood:	n/a	n/a
47	CEBPB	chr13:49948646-49949091	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr13:49995785-49995828	HepG2	liver:	n/a	n/a
49	CEBPB	chr13:50030370-50030619	IMR90	lung:	n/a	chr13:50030389-50030401
50	CEBPB	chr13:50039210-50039502	HepG2	liver:	n/a	n/a

(count:1709 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:50018157-50018207	PrEC	prostate:	n/a
2	chr13:50018157-50018207	PrEC	prostate:	n/a
3	chr13:50056284-50056334	T-47D	breast:	n/a
4	chr13:50056284-50056334	PrEC	prostate:	n/a
5	chr13:50018355-50018405	PrEC	prostate:	n/a
6	chr13:50024293-50024343	HL-60	blood:	n/a
7	chr13:50018531-50018581	HCPEpiC	choroid plexus:	n/a
8	chr13:49977110-49977160	HCM	heart:	n/a
9	chr13:50025780-50025830	ovcar-3	ovarian:	n/a
10	chr13:50018355-50018405	ovcar-3	ovarian:	n/a
11	chr13:50018157-50018207	HCM	heart:	n/a
12	chr13:50018044-50018094	IMR90	lung:	fetal
13	chr13:50056284-50056334	SKMC	muscle:	n/a
14	chr13:50030794-50030844	HCF	heart:	n/a
15	chr13:50018157-50018207	HNPCEpiC	eye:	n/a
16	chr13:50025780-50025830	HAEpiC	amniotic membrane:	n/a
17	chr13:50018409-50018459	SK-N-SH	brain:	n/a
18	chr13:50021335-50021385	IMR90	lung:	fetal
19	chr13:50018352-50018402	HCF	heart:	n/a
20	chr13:50018359-50018409	HUVEC	blood vessel:	n/a
21	chr13:50019081-50019131	HRCEpiC	kidney:	n/a
22	chr13:50018514-50018564	NT2-D1	testis:	n/a
23	chr13:49976473-49976523	AG09319	gingival:	n/a
24	chr13:50014904-50014954	AG04450	lung:	fetal
25	chr13:50024293-50024343	Caco-2	colon:	n/a
26	chr13:50030794-50030844	K562	blood:	n/a
27	chr13:49975643-49975693	H1-hESC	embryonic stem cell:	embryo
28	chr13:50018380-50018430	HL-60	blood:	n/a
29	chr13:50014904-50014954	T-47D	breast:	n/a
30	chr13:50018171-50018221	HNPCEpiC	eye:	n/a
31	chr13:49977110-49977160	AoSMC	blood vessel:	n/a
32	chr13:50024293-50024343	SK-N-SH	brain:	n/a
33	chr13:49975418-49975468	H1-hESC	embryonic stem cell:	embryo
34	chr13:49977110-49977160	U87	brain:	n/a
35	chr13:50024281-50024331	RPTEC	kidney:	n/a
36	chr13:50018406-50018456	NT2-D1	testis:	n/a
37	chr13:50018157-50018207	SKMC	muscle:	n/a
38	chr13:50018531-50018581	HEK293	kidney:	embryo
39	chr13:50018044-50018094	GM12891	blood:	n/a
40	chr13:49975383-49975433	HL-60	blood:	n/a
41	chr13:50018157-50018207	HIPEpiC	eye:	n/a
42	chr13:50018380-50018430	ProgFib	skin:	n/a
43	chr13:49990767-49990817	AG04449	skin:	fetal
44	chr13:50018636-50018686	PFSK-1	brain:	n/a
45	chr13:50030794-50030844	Hela-S3	cervix:	n/a
46	chr13:49975643-49975693	MCF10A-Er-Src	breast:	n/a
47	chr13:49975383-49975433	HepG2	liver:	n/a
48	chr13:50018531-50018581	LNCaP	prostate:	n/a
49	chr13:50025780-50025830	SK-N-SH_RA	brain:	n/a
50	chr13:49975383-49975433	HCM	heart:	n/a

(count:70 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr13:49874978..49875489-chr13:50010786..50011661,2	MCF-7	breast:
2	chr13:50017298..50020087-chr13:50026645..50030235,3	MCF-7	breast:
3	chr13:49874986..49875912-chr13:49995476..49996152,3	MCF-7	breast:
4	chr13:49978042..49980061-chr13:49981033..49983689,2	K562	blood:
5	chr13:50033311..50035354-chr13:50074002..50076664,2	MCF-7	breast:
6	chr13:50017638..50018206-chr6:35436122..35436718,2	NB4	blood:
7	chr13:49978561..49980656-chr13:49982189..49983984,2	K562	blood:
8	chr13:49971896..49974860-chr13:49997349..49999388,2	MCF-7	breast:
9	chr13:50013502..50016015-chr13:50068967..50071697,2	K562	blood:
10	chr13:50027049..50030534-chr13:50032779..50035441,4	K562	blood:
11	chr13:50011471..50014414-chr13:50018159..50020318,3	K562	blood:
12	chr13:50022438..50024030-chr13:50027384..50029296,2	MCF-7	breast:
13	chr13:50018375..50018943-chr9:33025160..33025792,2	NB4	blood:
14	chr13:49948746..49951030-chr13:49963060..49965178,2	K562	blood:
15	chr13:49978561..49980656-chr13:49982189..49983984,2	K562	blood:
16	chr13:50027025..50029589-chr13:50038716..50040663,2	MCF-7	breast:
17	chr10:10061157..10061825-chr13:49941866..49942517,2	MCF-7	breast:
18	chr13:50017920..50018425-chr3:127317278..127318186,2	NB4	blood:
19	chr13:50007202..50009372-chr13:50016314..50018307,2	K562	blood:
20	chr13:49937629..49939824-chr13:49947316..49949983,2	MCF-7	breast:
21	chr13:49875049..49876153-chr13:50010754..50011724,7	MCF-7	breast:
22	chr13:50017708..50019470-chr13:50036743..50039424,2	MCF-7	breast:
23	chr13:50016895..50018613-chr13:50024420..50026981,2	MCF-7	breast:
24	chr13:49994580..49997137-chr13:49999140..50001619,2	MCF-7	breast:
25	chr13:49975435..49977263-chr13:50015217..50018026,2	K562	blood:
26	chr13:49993633..49996417-chr13:50068251..50070383,2	K562	blood:
27	chr13:50022863..50025187-chr13:50116857..50119478,2	K562	blood:
28	chr13:50016481..50018378-chr13:50070335..50072171,3	K562	blood:
29	chr13:50020464..50022245-chr13:50034255..50036825,2	K562	blood:
30	chr13:49938960..49941756-chr13:49943750..49946277,2	K562	blood:
31	chr13:50010568..50013780-chr13:50016581..50020506,3	MCF-7	breast:
32	chr13:49668884..49671428-chr13:50017958..50020169,2	MCF-7	breast:
33	chr13:50022438..50024030-chr13:50027384..50029296,2	MCF-7	breast:
34	chr13:50018061..50019687-chr13:50035601..50037129,2	MCF-7	breast:
35	chr13:50007011..50008886-chr13:50012564..50014839,2	MCF-7	breast:
36	chr13:50038863..50040866-chr13:50041548..50043299,2	K562	blood:
37	chr13:49959574..49961755-chr13:50016698..50018510,2	MCF-7	breast:
38	chr13:50016638..50018754-chr19:46028466..46031236,2	MCF-7	breast:
39	chr13:50016508..50019619-chr13:50158297..50162493,5	MCF-7	breast:
40	chr13:50027025..50029589-chr13:50038716..50040663,2	MCF-7	breast:
41	chr13:49980803..49985123-chr13:49985194..49988213,3	MCF-7	breast:
42	chr13:49820702..49823407-chr13:50017509..50020339,3	MCF-7	breast:
43	chr13:49974198..49976511-chr13:50002118..50003753,2	MCF-7	breast:
44	chr13:50045650..50047733-chr13:50190939..50192914,2	MCF-7	breast:
45	chr13:50029751..50032528-chr13:50034704..50037567,2	MCF-7	breast:
46	chr13:50016483..50020444-chr13:50068529..50072853,4	MCF-7	breast:
47	chr13:49938960..49941756-chr13:49943750..49946277,2	K562	blood:
48	chr1:36554087..36554720-chr13:50018951..50019561,2	NB4	blood:
49	chr13:49978042..49980061-chr13:49981033..49983689,2	K562	blood:
50	chr13:50020071..50022197-chr13:50067941..50070115,2	K562	blood:

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL136218.1-1	chr13:49999396-49999977	NONHSAT033743
2	lnc-AL136218.1-2	chr13:49975269-49975406	NONHSAT033740
3	lnc-AL136218.1-2	chr13:49975632-49975723	NONHSAT033741
4	lnc-AL136218.1-2	chr13:50008222-50008359	NONHSAT033741
5	lnc-AL136218.1-2	chr13:49975531-49975723	NONHSAT033740
6	lnc-AL136218.1-1	chr13:49998089-49998144	NONHSAT033742
7	lnc-AL136218.1-2	chr13:49956643-49957077	NONHSAT033740
8	lnc-AL136218.1-2	chr13:49987048-49987176	NONHSAT033740
9	lnc-AL136218.1-1	chr13:49999416-49999586	NONHSAT033742
10	lnc-AL136218.1-2	chr13:49988140-49988335	NONHSAT033741
11	lnc-AL136218.1-1	chr13:49999345-49999351	NONHSAT033743
12	lnc-AL136218.1-2	chr13:50007454-50007529	NONHSAT033741
13	lnc-PHF11-2	chr13:50019689-50020088	NONHSAT033744
14	lnc-PHF11-2	chr13:50018820-50018993	NONHSAT033744
15	lnc-AL136218.1-1	chr13:49993070-49993573	NONHSAT033742
16	lnc-AL136218.1-2	chr13:50018122-50018200	NONHSAT033741

No data

Variant related genes	Relation type
SNRPGP14	TF binding region
CAB39L	TF binding region
SETDB2	TF binding region
ENSG00000215462	TF binding region
SNRPGP14	CpG island
CAB39L	CpG island
SETDB2	CpG island
ENSG00000215462	CpG island
ENSG00000116863	chromatin interactions
ENSG00000136147	chromatin interactions
ENSG00000215462	chromatin interactions
ENSG00000198755	chromatin interactions
ENSG00000136169	chromatin interactions
ENSG00000199788	chromatin interactions
ENSG00000017797	chromatin interactions
ENSG00000125753	chromatin interactions
ENSG00000102543	chromatin interactions
ENSG00000086061	chromatin interactions
ENSG00000137074	chromatin interactions
ENSG00000073111	chromatin interactions
ENSG00000102547	chromatin interactions
ENSG00000136144	chromatin interactions
ENSG00000006194	chromatin interactions
ENSG00000138279	chromatin interactions

Extended variants
information (count: 4351 )
Associated
traits (count: 126 )

Variant overlapped rSNPs/rCNVs (count:4351 , 50 per page) page: 1 2 3 4 5 6 7 ... 88

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9535203	chr13:49930643-49930644	Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs181690398	chr13:49930669-49930670	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs78393735	chr13:49930800-49930801	Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs573238239	chr13:49930802-49930803	Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs74072521	chr13:49930813-49930814	Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs35157732	chr13:49930838-49930839	Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs186322351	chr13:49930847-49930848	Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs35336598	chr13:49930904-49930905	Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs145719804	chr13:49930928-49930929	Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs577742608	chr13:49931013-49931014	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs530703489	chr13:49931029-49931030	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs552089456	chr13:49931051-49931052	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs570685798	chr13:49931100-49931101	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs528436765	chr13:49931110-49931111	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs546617557	chr13:49931134-49931135	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs191070811	chr13:49931171-49931172	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs11447143	chr13:49931185-49931186	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs148923105	chr13:49931189-49931190	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs397804263	chr13:49931199-49931200	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs182610320	chr13:49931235-49931236	Weak transcription Enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs187581681	chr13:49931243-49931244	Weak transcription Enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs9535204	chr13:49931258-49931259	Weak transcription Enhancers Strong transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs537608165	chr13:49931275-49931276	Weak transcription Enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs9535205	chr13:49931307-49931308	Weak transcription Enhancers Strong transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs577114847	chr13:49931314-49931315	Weak transcription Enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs143727590	chr13:49931378-49931379	Weak transcription Enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs552931254	chr13:49931379-49931380	Weak transcription Enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs574456058	chr13:49931411-49931412	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs547525597	chr13:49931420-49931421	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs372612055	chr13:49931486-49931487	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs78572658	chr13:49931490-49931491	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs541842883	chr13:49931515-49931516	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs563755196	chr13:49931522-49931523	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs376593185	chr13:49931543-49931544	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs146574348	chr13:49931549-49931550	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs200862592	chr13:49931555-49931556	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs202149230	chr13:49931556-49931557	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs141373881	chr13:49931576-49931577	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs530999223	chr13:49931578-49931579	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs79819200	chr13:49931616-49931617	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs549971732	chr13:49931621-49931622	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs543045961	chr13:49931640-49931641	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs191179489	chr13:49931672-49931673	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs550312113	chr13:49931691-49931692	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs568921373	chr13:49931761-49931762	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs563473246	chr13:49931764-49931765	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs138932494	chr13:49931793-49931794	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs368664189	chr13:49931822-49931823	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs532067914	chr13:49931852-49931853	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs78220121	chr13:49931911-49931912	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:126)

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	17899364	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
Trisomy	24170809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Alveolar rhabdomyosarcoma	16790082	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
Retinoblastoma	21504564	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Mental retardation	17502991	CNVD
Retinoblastoma	17502991	CNVD
Bipolar disorder	18458673	CNVD
Liposarcoma	21253554	CNVD
T-cell lymphomas	19863542	CNVD
Cervical cancer	21062161	CNVD
microdeletion syndrome	19284877	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
Chronic lymphocytic leukemia	21670202	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	19435819	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	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
Myelofibrosis	22110671	CNVD
Hereditary prostate cancer	22028916	CNVD
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Prostate cancer	17217626	CNVD
Ovarian cancer	21781307	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
Chronic myeloid leukemia	21384125	CNVD
Sezary syndrome	18413736	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21990379	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Alcoholism	21790672	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2660 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:49876200-49935600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
2	chr13:49884600-49933600	Weak transcription	Brain Cingulate Gyrus	brain
3	chr13:49885600-49933400	Weak transcription	Primary T cells from cord blood	blood
4	chr13:49889000-49944600	Weak transcription	Brain Angular Gyrus	brain
5	chr13:49889000-49947600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr13:49889200-49933400	Weak transcription	Brain Anterior Caudate	brain
7	chr13:49889200-49944600	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr13:49895600-49933200	Weak transcription	Primary hematopoietic stem cells	blood
9	chr13:49895800-49935600	Weak transcription	Esophagus	oesophagus
10	chr13:49904600-49930800	Weak transcription	Aorta	Aorta
11	chr13:49912600-49948800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr13:49913200-49932600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
13	chr13:49915000-49941400	Weak transcription	Brain Hippocampus Middle	brain
14	chr13:49922200-49937600	Weak transcription	Fetal Brain Male	brain
15	chr13:49922200-49937600	Weak transcription	Skeletal Muscle Female	skeletal muscle
16	chr13:49922400-49931800	Weak transcription	Left Ventricle	heart
17	chr13:49922400-49940800	Weak transcription	Lung	lung
18	chr13:49922400-49946600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr13:49922400-49947800	Weak transcription	Right Ventricle	heart
20	chr13:49922800-49951400	Weak transcription	Gastric	stomach
21	chr13:49923000-49935000	Weak transcription	Fetal Muscle Trunk	muscle
22	chr13:49923200-49934800	Weak transcription	Fetal Stomach	stomach
23	chr13:49923200-49935000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr13:49923200-49937800	Weak transcription	Primary B cells from cord blood	blood
25	chr13:49923200-49951200	Weak transcription	Pancreas	Pancrea
26	chr13:49925000-49930800	Weak transcription	Colon Smooth Muscle	Colon
27	chr13:49925000-49930800	Weak transcription	Duodenum Smooth Muscle	Duodenum
28	chr13:49926000-49933200	Weak transcription	Stomach Smooth Muscle	stomach
29	chr13:49926400-49934400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr13:49926400-49937600	Weak transcription	Brain Substantia Nigra	brain
31	chr13:49926800-49937800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr13:49928600-49932400	Enhancers	NHDF-Ad	bronchial
33	chr13:49929000-49936000	Weak transcription	Primary T helper cells fromperipheralblood	blood
34	chr13:49929200-49931200	Weak transcription	Adipose Nuclei	Adipose
35	chr13:49929400-49933400	Weak transcription	Fetal Heart	heart
36	chr13:49929400-49950000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr13:49929600-49931800	Weak transcription	Ovary	ovary
38	chr13:49929600-49934800	Weak transcription	Brain Germinal Matrix	brain
39	chr13:49929600-49936400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
40	chr13:49929800-49930800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr13:49929800-49931400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
42	chr13:49929800-49933000	Weak transcription	Fetal Brain Female	brain
43	chr13:49929800-49935200	Weak transcription	Skeletal Muscle Male	skeletal muscle
44	chr13:49929800-49937000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr13:49929800-49937600	Weak transcription	Liver	Liver
46	chr13:49930000-49930800	Enhancers	Muscle Satellite Cultured Cells	--
47	chr13:49930000-49932200	Enhancers	Rectal Smooth Muscle	rectum
48	chr13:49930000-49932200	Enhancers	HSMMtube	muscle
49	chr13:49930000-49932400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr13:49930000-49932400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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