Variant report

Variant	esv1807924
Chromosome Location	chr13:49991885-50036730
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1189)
CpG islands
(count:1282)
Chromatin interactive
region (count:47)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1189 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:50018043-50018342	K562	blood:	n/a	n/a
2	ARID3A	chr13:50022201-50022473	K562	blood:	n/a	n/a
3	ARID3A	chr13:50018824-50019531	K562	blood:	n/a	n/a
4	ARID3A	chr13:50017884-50018589	HepG2	liver:	n/a	n/a
5	ARID3A	chr13:49995639-49995842	HepG2	liver:	n/a	n/a
6	ATF2	chr13:50017722-50018650	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr13:50028627-50029260	GM12878	blood:	n/a	n/a
8	ATF2	chr13:50017524-50018660	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr13:50017921-50018315	GM12878	blood:	n/a	n/a
10	ATF2	chr13:50028547-50029303	GM12878	blood:	n/a	n/a
11	ATF2	chr13:50017799-50018696	GM12878	blood:	n/a	n/a
12	BATF	chr13:50028595-50029091	GM12878	blood:	n/a	n/a
13	BATF	chr13:50028580-50029122	GM12878	blood:	n/a	n/a
14	BATF	chr13:50033735-50034011	GM12878	blood:	n/a	n/a
15	BATF	chr13:50033761-50033980	GM12878	blood:	n/a	n/a
16	BCLAF1	chr13:50017479-50018901	GM12878	blood:	n/a	chr13:50018730-50018743
17	BCLAF1	chr13:50017854-50018762	GM12878	blood:	n/a	chr13:50018730-50018743
18	BHLHE40	chr13:49995589-49995906	HepG2	liver:	n/a	n/a
19	BHLHE40	chr13:50017572-50017700	HepG2	liver:	n/a	n/a
20	BHLHE40	chr13:50028754-50029257	GM12878	blood:	n/a	n/a
21	BHLHE40	chr13:50017924-50019861	GM12878	blood:	n/a	n/a
22	BHLHE40	chr13:50017907-50019581	K562	blood:	n/a	n/a
23	BHLHE40	chr13:50019165-50019509	A549	lung:	n/a	n/a
24	BHLHE40	chr13:50019167-50019537	HepG2	liver:	n/a	n/a
25	BRCA1	chr13:50017752-50018443	H1-hESC	embryonic stem cell:	n/a	n/a
26	BRCA1	chr13:50017958-50018595	HepG2	liver:	n/a	n/a
27	BRCA1	chr13:50017808-50018576	GM12878	blood:	n/a	n/a
28	BRCA1	chr13:50017797-50019617	Hela-S3	cervix:	n/a	n/a
29	CBX3	chr13:50017976-50018310	K562	blood:	n/a	n/a
30	CBX3	chr13:50017739-50018627	K562	blood:	n/a	n/a
31	CCNT2	chr13:50018091-50019133	K562	blood:	n/a	chr13:50018752-50018761
32	CEBPB	chr13:50011962-50012062	HepG2	liver:	n/a	chr13:50012012-50012023
33	CEBPB	chr13:50017986-50018199	HepG2	liver:	n/a	n/a
34	CEBPB	chr13:50030370-50030619	IMR90	lung:	n/a	chr13:50030389-50030401
35	CEBPB	chr13:50018081-50018270	K562	blood:	n/a	n/a
36	CEBPB	chr13:50011867-50012135	H1-hESC	embryonic stem cell:	n/a	chr13:50012012-50012023
37	CEBPB	chr13:50028602-50029333	GM12878	blood:	n/a	n/a
38	CEBPB	chr13:50018054-50018646	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr13:49995785-49995828	HepG2	liver:	n/a	n/a
40	CEBPD	chr13:50018365-50018760	HepG2	liver:	n/a	n/a
41	CEBPD	chr13:50018784-50019236	K562	blood:	n/a	n/a
42	CHD1	chr13:50017449-50019775	GM12878	blood:	n/a	n/a
43	CHD1	chr13:50017197-50018140	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD1	chr13:50018630-50018907	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD2	chr13:50017584-50018692	K562	blood:	n/a	n/a
46	CHD2	chr13:50017725-50018730	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD2	chr13:50028816-50029133	GM12878	blood:	n/a	n/a
48	CHD2	chr13:50017898-50018851	HepG2	liver:	n/a	n/a
49	CHD2	chr13:50017490-50019597	GM12878	blood:	n/a	n/a
50	CHD2	chr13:49995508-49995840	HepG2	liver:	n/a	n/a

(count:1282 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:50018531-50018581	AG09309	skin:	n/a
2	chr13:50018531-50018581	AG09309	skin:	n/a
3	chr13:50030794-50030844	Hela-S3	cervix:	n/a
4	chr13:50018137-50018187	AG09319	gingival:	n/a
5	chr13:50018352-50018402	AoSMC	blood vessel:	n/a
6	chr13:50014904-50014954	ProgFib	skin:	n/a
7	chr13:50024703-50024753	ECC-1	luminal epithelium:	n/a
8	chr13:50018380-50018430	HepG2	liver:	n/a
9	chr13:50018514-50018564	CMK	blood:	n/a
10	chr13:50018359-50018409	LNCaP	prostate:	n/a
11	chr13:50018380-50018430	GM12892	blood:	n/a
12	chr13:50018044-50018094	H1-hESC	embryonic stem cell:	embryo
13	chr13:50018355-50018405	PrEC	prostate:	n/a
14	chr13:50030794-50030844	Jurkat	blood:	n/a
15	chr13:50018514-50018564	GM12891	blood:	n/a
16	chr13:50018514-50018564	A549	lung:	n/a
17	chr13:50024293-50024343	GM12892	blood:	n/a
18	chr13:50018406-50018456	Hela-S3	cervix:	n/a
19	chr13:50024281-50024331	SK-N-MC	brain:	n/a
20	chr13:50018380-50018430	GM19239	blood:	n/a
21	chr13:50018531-50018581	SK-N-SH	brain:	n/a
22	chr13:50018171-50018221	GM06990	blood:	n/a
23	chr13:50024703-50024753	GM12878	blood:	n/a
24	chr13:50018359-50018409	AG10803	skin:	n/a
25	chr13:50021335-50021385	Hepatocyte	liver:	n/a
26	chr13:50018409-50018459	PANC-1	pancreas:	n/a
27	chr13:50018171-50018221	SK-N-MC	brain:	n/a
28	chr13:50021335-50021385	BE2_C	brain:	n/a
29	chr13:50024281-50024331	NB4	blood:	n/a
30	chr13:50018157-50018207	IMR90	lung:	fetal
31	chr13:50014904-50014954	A549	lung:	n/a
32	chr13:50018352-50018402	MCF10A-Er-Src	breast:	n/a
33	chr13:50018531-50018581	K562	blood:	n/a
34	chr13:50018636-50018686	BJ	skin:	n/a
35	chr13:50018171-50018221	ECC-1	luminal epithelium:	n/a
36	chr13:50018531-50018581	HRCEpiC	kidney:	n/a
37	chr13:50018044-50018094	HAEpiC	amniotic membrane:	n/a
38	chr13:50018137-50018187	HMEC	breast:	n/a
39	chr13:50014904-50014954	HCT-116	colon:	n/a
40	chr13:50018406-50018456	HL-60	blood:	n/a
41	chr13:50014904-50014954	HNPCEpiC	eye:	n/a
42	chr13:50018044-50018094	K562	blood:	n/a
43	chr13:50018157-50018207	GM12878	blood:	n/a
44	chr13:50018355-50018405	HNPCEpiC	eye:	n/a
45	chr13:50018355-50018405	HIPEpiC	eye:	n/a
46	chr13:50025780-50025830	HRE	kidney:	n/a
47	chr13:50018406-50018456	A549	lung:	n/a
48	chr13:50018531-50018581	HEK293	kidney:	embryo
49	chr13:50018409-50018459	Jurkat	blood:	n/a
50	chr13:50018636-50018686	AG09309	skin:	n/a

(count:47 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:50027025..50029589-chr13:50038716..50040663,2	MCF-7	breast:
2	chr13:49820441..49822930-chr13:50018500..50020473,2	K562	blood:
3	chr13:49874986..49875912-chr13:49995476..49996152,3	MCF-7	breast:
4	chr13:49993633..49996417-chr13:50068251..50070383,2	K562	blood:
5	chr13:50010568..50013780-chr13:50016581..50020506,3	MCF-7	breast:
6	chr13:50017920..50018425-chr3:127317278..127318186,2	NB4	blood:
7	chr13:50018375..50018943-chr9:33025160..33025792,2	NB4	blood:
8	chr13:50007011..50008886-chr13:50012564..50014839,2	MCF-7	breast:
9	chr13:49975435..49977263-chr13:50015217..50018026,2	K562	blood:
10	chr13:50011471..50014414-chr13:50018159..50020318,3	K562	blood:
11	chr13:49971896..49974860-chr13:49997349..49999388,2	MCF-7	breast:
12	chr13:50007011..50008886-chr13:50012564..50014839,2	MCF-7	breast:
13	chr13:50027049..50030534-chr13:50032779..50035441,4	K562	blood:
14	chr13:50007202..50009372-chr13:50016314..50018307,2	K562	blood:
15	chr13:49875049..49876153-chr13:50010754..50011724,7	MCF-7	breast:
16	chr13:50017638..50018206-chr6:35436122..35436718,2	NB4	blood:
17	chr13:50016638..50018754-chr19:46028466..46031236,2	MCF-7	breast:
18	chr13:50022438..50024030-chr13:50027384..50029296,2	MCF-7	breast:
19	chr13:50017298..50020087-chr13:50026645..50030235,3	MCF-7	breast:
20	chr13:50020071..50022197-chr13:50067941..50070115,2	K562	blood:
21	chr13:50022863..50025187-chr13:50116857..50119478,2	K562	blood:
22	chr13:50016895..50018613-chr13:50024420..50026981,2	MCF-7	breast:
23	chr13:50016715..50020360-chr13:50068508..50074036,7	MCF-7	breast:
24	chr13:50020031..50021593-chr13:50030911..50032935,2	MCF-7	breast:
25	chr13:50029751..50032528-chr13:50034704..50037567,2	MCF-7	breast:
26	chr13:50013502..50016015-chr13:50068967..50071697,2	K562	blood:
27	chr13:49820702..49823407-chr13:50017509..50020339,3	MCF-7	breast:
28	chr13:50016481..50018378-chr13:50070335..50072171,3	K562	blood:
29	chr13:50016992..50019784-chr13:50159235..50161344,2	K562	blood:
30	chr13:50018060..50018635-chr18:9475189..9475739,2	NB4	blood:
31	chr13:50016440..50019751-chr13:50141127..50144444,4	MCF-7	breast:
32	chr13:49994580..49997137-chr13:49999140..50001619,2	MCF-7	breast:
33	chr13:49668884..49671428-chr13:50017958..50020169,2	MCF-7	breast:
34	chr10:75173616..75174305-chr13:50017762..50018728,2	HCT-116	colon:
35	chr13:50016483..50020444-chr13:50068529..50072853,4	MCF-7	breast:
36	chr13:50022438..50024030-chr13:50027384..50029296,2	MCF-7	breast:
37	chr13:50027049..50030534-chr13:50032779..50035441,4	K562	blood:
38	chr13:50033311..50035354-chr13:50074002..50076664,2	MCF-7	breast:
39	chr13:50029751..50032528-chr13:50034704..50037567,2	MCF-7	breast:
40	chr13:49874978..49875489-chr13:50010786..50011661,2	MCF-7	breast:
41	chr13:50020464..50022245-chr13:50034255..50036825,2	K562	blood:
42	chr13:49974198..49976511-chr13:50002118..50003753,2	MCF-7	breast:
43	chr13:50016508..50019619-chr13:50158297..50162493,5	MCF-7	breast:
44	chr13:50017253..50018810-chr16:3331703..3334184,2	MCF-7	breast:
45	chr13:49875221..49876253-chr13:50010820..50011928,3	K562	blood:
46	chr1:36554087..36554720-chr13:50018951..50019561,2	NB4	blood:
47	chr13:50018061..50019687-chr13:50035601..50037129,2	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL136218.1-1	chr13:49993070-49993573	NONHSAT033742
2	lnc-AL136218.1-2	chr13:50018122-50018200	NONHSAT033741
3	lnc-AL136218.1-1	chr13:49999416-49999586	NONHSAT033742
4	lnc-AL136218.1-1	chr13:49999345-49999351	NONHSAT033743
5	lnc-AL136218.1-2	chr13:50008222-50008359	NONHSAT033741
6	lnc-AL136218.1-1	chr13:49998089-49998144	NONHSAT033742
7	lnc-AL136218.1-1	chr13:49999396-49999977	NONHSAT033743
8	lnc-PHF11-2	chr13:50019689-50020088	NONHSAT033744
9	lnc-AL136218.1-2	chr13:50007454-50007529	NONHSAT033741
10	lnc-PHF11-2	chr13:50018820-50018993	NONHSAT033744

No data

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

Extended variants
information (count: 1502 )
Associated
traits (count: 122 )

Variant overlapped rSNPs/rCNVs (count:1502 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs79502368	chr13:49991942-49991943	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs7328755	chr13:49991949-49991950	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs559320692	chr13:49991963-49991964	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs577308151	chr13:49991965-49991966	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs569503546	chr13:49991976-49991977	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs145469888	chr13:49992016-49992017	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs574831816	chr13:49992030-49992031	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs541983180	chr13:49992049-49992050	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs563465872	chr13:49992115-49992116	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs9316449	chr13:49992128-49992129	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs368718104	chr13:49992165-49992166	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs79899257	chr13:49992210-49992211	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs28591539	chr13:49992226-49992227	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs181813505	chr13:49992336-49992337	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs137992245	chr13:49992486-49992487	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs141142796	chr13:49992497-49992498	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs115521068	chr13:49992524-49992525	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs375476440	chr13:49992555-49992556	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs528948586	chr13:49992574-49992575	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs372624835	chr13:49992591-49992592	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs186299232	chr13:49992599-49992600	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs570209620	chr13:49992632-49992633	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs144864506	chr13:49992638-49992639	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs552895515	chr13:49992646-49992647	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs148309121	chr13:49992650-49992651	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs376703283	chr13:49992734-49992735	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs79692375	chr13:49992778-49992779	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs116051383	chr13:49992800-49992801	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs191039219	chr13:49992815-49992816	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs568380640	chr13:49992927-49992928	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs141411447	chr13:49992966-49992967	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs183549508	chr13:49992988-49992989	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs575383555	chr13:49993022-49993023	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs73188635	chr13:49993087-49993088	Enhancers Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs536168135	chr13:49993136-49993137	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
36	rs150811549	chr13:49993166-49993167	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
37	rs540151904	chr13:49993169-49993170	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
38	rs561708176	chr13:49993172-49993173	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
39	rs528909178	chr13:49993194-49993195	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
40	rs186756737	chr13:49993195-49993196	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs562486085	chr13:49993199-49993200	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs533057318	chr13:49993248-49993249	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
43	rs531433397	chr13:49993260-49993261	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
44	rs7336188	chr13:49993292-49993293	Enhancers Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs190914319	chr13:49993323-49993324	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
46	rs527248346	chr13:49993328-49993329	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
47	rs143897535	chr13:49993350-49993351	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
48	rs547354147	chr13:49993369-49993370	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
49	rs9591259	chr13:49993384-49993385	Enhancers Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs556139150	chr13:49993442-49993443	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:122)

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

Chromatin state (count:1238 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:49975600-49993600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr13:49975600-50001000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr13:49975800-50001600	Weak transcription	Fetal Stomach	stomach
4	chr13:49975800-50013600	Weak transcription	Primary B cells from cord blood	blood
5	chr13:49976000-49992800	Weak transcription	Ovary	ovary
6	chr13:49978400-50005400	Weak transcription	Aorta	Aorta
7	chr13:49978400-50016800	Weak transcription	Fetal Brain Male	brain
8	chr13:49979800-49997200	Weak transcription	Left Ventricle	heart
9	chr13:49980400-50006400	Weak transcription	Duodenum Smooth Muscle	Duodenum
10	chr13:49981600-49993200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr13:49983400-50017000	Weak transcription	Brain Anterior Caudate	brain
12	chr13:49983400-50017400	Weak transcription	Lung	lung
13	chr13:49983600-50017000	Weak transcription	Brain Angular Gyrus	brain
14	chr13:49984400-50001200	Weak transcription	Stomach Smooth Muscle	stomach
15	chr13:49984400-50010200	Weak transcription	Brain Substantia Nigra	brain
16	chr13:49985000-50001200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr13:49986800-49998000	Weak transcription	Adipose Nuclei	Adipose
18	chr13:49988200-49995600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr13:49988600-49993000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr13:49989200-50006800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr13:49989800-49993400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr13:49991200-49992800	Enhancers	Primary neutrophils fromperipheralblood	blood
23	chr13:49991200-49993000	Enhancers	Monocytes-CD14+_RO01746	blood
24	chr13:49991400-49993000	Enhancers	Primary monocytes fromperipheralblood	blood
25	chr13:49991800-49994200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr13:49992200-49992600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr13:49992200-49993200	Enhancers	Primary hematopoietic stem cells short term culture	blood
28	chr13:49992400-49994000	Enhancers	HepG2	liver
29	chr13:49992800-49993800	Enhancers	Ovary	ovary
30	chr13:49992800-49993800	Weak transcription	HSMM	muscle
31	chr13:49993000-49994200	Enhancers	Muscle Satellite Cultured Cells	--
32	chr13:49993000-49994200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
33	chr13:49993000-49994600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr13:49993000-49994800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr13:49993200-49993800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr13:49993200-49994600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr13:49993400-49993800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr13:49993400-49994000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr13:49993600-49994000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr13:49993600-49994000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr13:49993600-49994000	Enhancers	NHDF-Ad	bronchial
42	chr13:49993800-49994000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr13:49993800-49994000	Enhancers	HSMM	muscle
44	chr13:49993800-49994000	Enhancers	NHLF	lung
45	chr13:49993800-49994000	Enhancers	Osteobl	bone
46	chr13:49993800-49994800	Enhancers	HSMMtube	muscle
47	chr13:49993800-49995200	Weak transcription	Ovary	ovary
48	chr13:49993800-50001600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr13:49993800-50017400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr13:49994000-49994200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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