Variant report

Variant	esv3434605
Chromosome Location	chr13:52999509-53034851
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1606)
CpG islands
(count:1587)
Chromatin interactive
region (count:39)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1606 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:53029122-53030383	HepG2	liver:	n/a	n/a
2	ARID3A	chr13:53024613-53025199	HepG2	liver:	n/a	n/a
3	ARID3A	chr13:53023945-53024413	HepG2	liver:	n/a	n/a
4	ARID3A	chr13:53024736-53024977	K562	blood:	n/a	n/a
5	ARID3A	chr13:53002461-53002786	HepG2	liver:	n/a	n/a
6	ATF2	chr13:53028559-53029467	GM12878	blood:	n/a	n/a
7	ATF2	chr13:53024535-53024981	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr13:53024549-53024982	GM12878	blood:	n/a	n/a
9	ATF2	chr13:53024580-53024959	GM12878	blood:	n/a	n/a
10	ATF2	chr13:53028420-53029582	GM12878	blood:	n/a	n/a
11	ATF2	chr13:53023939-53024398	GM12878	blood:	n/a	n/a
12	ATF3	chr13:53024613-53024954	A549	lung:	n/a	n/a
13	BACH1	chr13:53024652-53025040	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr13:53029095-53029647	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr13:53032296-53032472	GM12878	blood:	n/a	n/a
16	BATF	chr13:53021605-53021781	GM12878	blood:	n/a	n/a
17	BCL11A	chr13:53024599-53024941	GM12878	blood:	n/a	chr13:53024859-53024872
18	BCL11A	chr13:53029009-53029234	GM12878	blood:	n/a	chr13:53029065-53029074
19	BCL11A	chr13:53028636-53028839	GM12878	blood:	n/a	n/a
20	BCL11A	chr13:53028605-53028936	GM12878	blood:	n/a	n/a
21	BCL11A	chr13:53028983-53029269	GM12878	blood:	n/a	chr13:53029065-53029074
22	BCL3	chr13:53024597-53025097	A549	lung:	n/a	chr13:53024859-53024872
23	BCL3	chr13:53024592-53025005	GM12878	blood:	n/a	chr13:53024859-53024872
24	BCLAF1	chr13:53028928-53030037	GM12878	blood:	n/a	chr13:53029620-53029629 chr13:53029065-53029074
25	BCLAF1	chr13:53024567-53025083	K562	blood:	n/a	chr13:53024859-53024872
26	BCLAF1	chr13:53023968-53025081	GM12878	blood:	n/a	chr13:53024859-53024872
27	BCLAF1	chr13:53024086-53025106	GM12878	blood:	n/a	chr13:53024859-53024872
28	BCLAF1	chr13:53028494-53029866	GM12878	blood:	n/a	chr13:53029620-53029629 chr13:53029065-53029074
29	BHLHE40	chr13:53029071-53030081	K562	blood:	n/a	chr13:53029571-53029587
30	BHLHE40	chr13:53024007-53025093	K562	blood:	n/a	n/a
31	BHLHE40	chr13:53024005-53025076	HepG2	liver:	n/a	n/a
32	BHLHE40	chr13:53028505-53030183	GM12878	blood:	n/a	chr13:53029571-53029587
33	BHLHE40	chr13:53028221-53028316	K562	blood:	n/a	n/a
34	BHLHE40	chr13:53023945-53025086	GM12878	blood:	n/a	n/a
35	BRCA1	chr13:53024062-53024400	Hela-S3	cervix:	n/a	n/a
36	BRCA1	chr13:53028262-53029683	Hela-S3	cervix:	n/a	n/a
37	BRCA1	chr13:53023517-53023692	Hela-S3	cervix:	n/a	n/a
38	BRCA1	chr13:53024575-53025037	HepG2	liver:	n/a	n/a
39	BRCA1	chr13:53024667-53024972	GM12878	blood:	n/a	n/a
40	BRCA1	chr13:53029337-53029848	HepG2	liver:	n/a	n/a
41	BRCA1	chr13:53024653-53024930	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chr13:53024710-53025083	H1-hESC	embryonic stem cell:	n/a	n/a
43	CBX3	chr13:53029190-53029706	K562	blood:	n/a	n/a
44	CBX3	chr13:53024559-53025092	K562	blood:	n/a	n/a
45	CCNT2	chr13:53024033-53025093	K562	blood:	n/a	n/a
46	CCNT2	chr13:53028724-53030228	K562	blood:	n/a	chr13:53030156-53030165 chr13:53030075-53030084
47	CEBPB	chr13:53024006-53024279	A549	lung:	n/a	n/a
48	CEBPB	chr13:53022203-53022444	Hela-S3	cervix:	n/a	chr13:53022338-53022351 chr13:53022338-53022351 chr13:53022339-53022350
49	CEBPB	chr13:53024739-53024975	K562	blood:	n/a	n/a
50	CEBPB	chr13:53020430-53020759	HepG2	liver:	n/a	chr13:53020586-53020597

(count:1587 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:53029438-53029488	BE2_C	brain:	n/a
2	chr13:53029438-53029488	BE2_C	brain:	n/a
3	chr13:53024717-53024767	ovcar-3	ovarian:	n/a
4	chr13:53029148-53029198	H1-hESC	embryonic stem cell:	embryo
5	chr13:53025003-53025053	NB4	blood:	n/a
6	chr13:53029588-53029638	HEK293	kidney:	embryo
7	chr13:53024733-53024783	CMK	blood:	n/a
8	chr13:53024905-53024955	CMK	blood:	n/a
9	chr13:53029627-53029677	GM12892	blood:	n/a
10	chr13:53033788-53033838	NT2-D1	testis:	n/a
11	chr13:53024156-53024206	BJ	skin:	n/a
12	chr13:53023979-53024029	NT2-D1	testis:	n/a
13	chr13:53024905-53024955	T-47D	breast:	n/a
14	chr13:53024934-53024984	AG10803	skin:	n/a
15	chr13:53029627-53029677	GM12878	blood:	n/a
16	chr13:53023979-53024029	MCF10A-Er-Src	breast:	n/a
17	chr13:53024912-53024962	HepG2	liver:	n/a
18	chr13:53029591-53029641	NHBE	bronchial:	n/a
19	chr13:53029211-53029261	Jurkat	blood:	n/a
20	chr13:53029588-53029638	HepG2	liver:	n/a
21	chr13:53024905-53024955	SK-N-SH	brain:	n/a
22	chr13:53029954-53030004	HepG2	liver:	n/a
23	chr13:53025762-53025812	HIPEpiC	eye:	n/a
24	chr13:53029355-53029405	A549	lung:	n/a
25	chr13:53025762-53025812	AG04449	skin:	fetal
26	chr13:53029438-53029488	HCM	heart:	n/a
27	chr13:53029588-53029638	HPAEpiC	pulmonary alveolar:	n/a
28	chr13:53025003-53025053	HCM	heart:	n/a
29	chr13:53029422-53029472	GM19239	blood:	n/a
30	chr13:53030145-53030195	SAEC	small airway:	n/a
31	chr13:53025608-53025658	BJ	skin:	n/a
32	chr13:53029418-53029468	HCF	heart:	n/a
33	chr13:53029211-53029261	CMK	blood:	n/a
34	chr13:53029438-53029488	HNPCEpiC	eye:	n/a
35	chr13:53029591-53029641	HRPEpiC	eye:	n/a
36	chr13:53029954-53030004	GM19239	blood:	n/a
37	chr13:53033788-53033838	SK-N-SH_RA	brain:	n/a
38	chr13:53025608-53025658	PANC-1	pancreas:	n/a
39	chr13:53033788-53033838	Caco-2	colon:	n/a
40	chr13:53029438-53029488	GM12878	blood:	n/a
41	chr13:53024439-53024489	GM06990	blood:	n/a
42	chr13:53029385-53029435	HL-60	blood:	n/a
43	chr13:53025762-53025812	HNPCEpiC	eye:	n/a
44	chr13:53024934-53024984	PrEC	prostate:	n/a
45	chr13:53024912-53024962	GM19239	blood:	n/a
46	chr13:53029438-53029488	HIPEpiC	eye:	n/a
47	chr13:53029422-53029472	HRE	kidney:	n/a
48	chr13:53024912-53024962	H1-hESC	embryonic stem cell:	embryo
49	chr13:53029438-53029488	LNCaP	prostate:	n/a
50	chr13:53029954-53030004	HCPEpiC	choroid plexus:	n/a

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:53029326..53030088-chr16:2204666..2205482,2	Hela-S3	cervix:
2	chr13:53011091..53012945-chr13:53024364..53026884,2	MCF-7	breast:
3	chr13:53016259..53019083-chr13:53028600..53030221,2	MCF-7	breast:
4	chr13:53034318..53035830-chr13:53040795..53043273,2	MCF-7	breast:
5	chr13:53015538..53018877-chr13:53019093..53022544,5	MCF-7	breast:
6	chr13:53031068..53033072-chr13:53251817..53253830,2	K562	blood:
7	chr13:53002808..53004729-chr13:53008103..53010876,2	MCF-7	breast:
8	chr13:52025591..52028546-chr13:53016299..53018785,2	K562	blood:
9	chr13:53015095..53017013-chr13:53020968..53022878,2	MCF-7	breast:
10	chr13:52985298..52988100-chr13:53012949..53014836,2	K562	blood:
11	chr13:52377836..52379871-chr13:53028245..53029773,2	K562	blood:
12	chr1:201979261..201979842-chr13:53024291..53024954,2	Hela-S3	cervix:
13	chr13:53029063..53030012-chrX:153718459..153719167,2	Hela-S3	cervix:
14	chr13:52973921..52974578-chr13:53024315..53025276,3	MCF-7	breast:
15	chr13:52989175..52991145-chr13:53028466..53031085,2	MCF-7	breast:
16	chr13:53014003..53016832-chr13:53024151..53026881,3	MCF-7	breast:
17	chr13:53034739..53038447-chr13:53039311..53042950,6	K562	blood:
18	chr13:53024565..53025183-chr2:239148354..239149000,2	HCT-116	colon:
19	chr13:53023259..53027625-chr13:53027753..53030727,5	MCF-7	breast:
20	chr13:53015538..53018877-chr13:53019093..53022544,5	MCF-7	breast:
21	chr13:53023588..53025754-chr13:53225469..53228375,2	K562	blood:
22	chr13:53028109..53029845-chr13:53190052..53193351,3	MCF-7	breast:
23	chr13:53017329..53018919-chr13:53022687..53024858,2	K562	blood:
24	chr1:155023406..155024318-chr13:53029329..53030119,2	NB4	blood:
25	chr13:52025134..52027888-chr13:53029090..53030597,2	MCF-7	breast:
26	chr13:53028631..53030845-chr13:53030982..53032693,2	MCF-7	breast:
27	chr13:53029255..53030110-chr8:54934384..54934889,2	HCT-116	colon:
28	chr13:53023126..53025517-chr17:56734157..56736833,2	MCF-7	breast:
29	chr12:53344450..53346377-chr13:53029194..53030956,2	MCF-7	breast:
30	chr13:53025603..53028034-chr13:53044066..53046923,2	K562	blood:
31	chr13:53017677..53022269-chr13:53022442..53026165,6	MCF-7	breast:
32	chr13:52993615..52996128-chr13:52998035..53000509,2	K562	blood:
33	chr13:53023259..53027625-chr13:53027753..53030727,5	MCF-7	breast:
34	chr13:52911600..52913908-chr13:53027001..53029186,3	MCF-7	breast:
35	chr13:53028078..53032210-chr13:53033257..53037371,7	MCF-7	breast:
36	chr13:53033923..53036375-chr13:53036479..53039026,2	K562	blood:
37	chr13:53011049..53014413-chr13:53028431..53030493,3	K562	blood:
38	chr13:53015095..53017013-chr13:53020968..53022878,2	MCF-7	breast:
39	chr13:53000967..53003487-chr13:53023394..53025748,2	MCF-7	breast:

No data

Variant related genes	Relation type
VPS36	TF binding region
CKAP2	TF binding region
VPS36	CpG island
CKAP2	CpG island
ENSG00000144485	chromatin interactions
ENSG00000236778	chromatin interactions
ENSG00000265039	chromatin interactions
ENSG00000163435	chromatin interactions
ENSG00000231856	chromatin interactions
ENSG00000250299	chromatin interactions
ENSG00000206630	chromatin interactions
ENSG00000187735	chromatin interactions
ENSG00000136100	chromatin interactions
ENSG00000102796	chromatin interactions
ENSG00000224892	chromatin interactions
ENSG00000143537	chromatin interactions
ENSG00000111057	chromatin interactions
ENSG00000260260	chromatin interactions
ENSG00000102786	chromatin interactions
ENSG00000199605	chromatin interactions
ENSG00000126903	chromatin interactions
ENSG00000136108	chromatin interactions
ENSG00000202077	chromatin interactions
ENSG00000165416	chromatin interactions
ENSG00000234678	chromatin interactions
ENSG00000139675	chromatin interactions

Extended variants
information (count: 1346 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:1346 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538021566	chr13:52999516-52999517	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs141375010	chr13:52999552-52999553	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs61958051	chr13:52999583-52999584	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs61958052	chr13:52999595-52999596	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs554162455	chr13:52999641-52999642	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs574395980	chr13:52999671-52999672	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs61958053	chr13:52999726-52999727	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs563118290	chr13:52999834-52999835	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs145104980	chr13:52999870-52999871	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs545575157	chr13:52999921-52999922	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs371686906	chr13:52999941-52999942	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs373315037	chr13:52999951-52999952	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs370714887	chr13:52999952-52999953	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs78757814	chr13:52999989-52999990	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs114035321	chr13:53000009-53000010	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs370328744	chr13:53000031-53000032	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs200170312	chr13:53000038-53000039	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs546200958	chr13:53000044-53000045	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs372964258	chr13:53000049-53000050	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs377501808	chr13:53000109-53000110	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs148021124	chr13:53000112-53000113	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs148016251	chr13:53000136-53000137	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs371044193	chr13:53000245-53000246	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs529173335	chr13:53000252-53000253	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs35543678	chr13:53000304-53000305	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs548891369	chr13:53000333-53000334	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs185151941	chr13:53000392-53000393	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs531444003	chr13:53000420-53000421	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs551548267	chr13:53000421-53000422	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs571652332	chr13:53000459-53000460	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs117734929	chr13:53000487-53000488	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs112836096	chr13:53000548-53000549	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs375798989	chr13:53000571-53000572	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs141670176	chr13:53000589-53000590	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs150092845	chr13:53000600-53000601	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs536633286	chr13:53000632-53000633	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs115131783	chr13:53000662-53000663	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs576670758	chr13:53000701-53000702	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs545276217	chr13:53000722-53000723	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs559069831	chr13:53000734-53000735	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs577336594	chr13:53000741-53000742	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs539914846	chr13:53000773-53000774	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs559796324	chr13:53000816-53000817	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs528889888	chr13:53000817-53000818	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs531638359	chr13:53000823-53000824	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs61570509	chr13:53000832-53000833	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs57540180	chr13:53000834-53000835	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs373319222	chr13:53000846-53000847	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs138361495	chr13:53000847-53000848	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs142902630	chr13:53000850-53000851	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:109)

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

Chromatin state (count:2207 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:52980200-53002000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr13:52980200-53021600	Weak transcription	Small Intestine	intestine
3	chr13:52981000-53022800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr13:52982800-53012600	Weak transcription	Fetal Brain Male	brain
5	chr13:52983600-53000800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
6	chr13:52983800-53016600	Strong transcription	Primary monocytes fromperipheralblood	blood
7	chr13:52984000-53002400	Weak transcription	Hela-S3	cervix
8	chr13:52984400-53023400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr13:52984800-53013400	Strong transcription	Dnd41	blood
10	chr13:52985000-53000600	Strong transcription	Duodenum Smooth Muscle	Duodenum
11	chr13:52985000-53001400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr13:52985000-53002400	Weak transcription	K562	blood
13	chr13:52985000-53013400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr13:52985000-53017400	Strong transcription	Monocytes-CD14+_RO01746	blood
15	chr13:52985000-53019400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
16	chr13:52985600-53000800	Strong transcription	Fetal Muscle Trunk	muscle
17	chr13:52985600-53004000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr13:52985600-53010600	Strong transcription	Rectal Mucosa Donor 29	rectum
19	chr13:52985800-53001400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
20	chr13:52986000-53017000	Strong transcription	Primary B cells from peripheral blood	blood
21	chr13:52986200-53001600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
22	chr13:52986600-53013400	Strong transcription	Liver	Liver
23	chr13:52986800-53002400	Weak transcription	Stomach Mucosa	stomach
24	chr13:52987000-53004200	Strong transcription	Primary T helper cells PMA-I stimulated	--
25	chr13:52987200-53023600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
26	chr13:52988000-53001200	Strong transcription	Skeletal Muscle Female	skeletal muscle
27	chr13:52988200-53001200	Strong transcription	Stomach Smooth Muscle	stomach
28	chr13:52988400-53001400	Strong transcription	Fetal Thymus	thymus
29	chr13:52988800-53002600	Weak transcription	Psoas Muscle	Psoas
30	chr13:52988800-53010000	Weak transcription	Esophagus	oesophagus
31	chr13:52989000-53003400	Weak transcription	Gastric	stomach
32	chr13:52989000-53006000	Weak transcription	NHLF	lung
33	chr13:52989000-53015000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr13:52989000-53016200	Strong transcription	Adipose Nuclei	Adipose
35	chr13:52989000-53021600	Weak transcription	Fetal Heart	heart
36	chr13:52989000-53022800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr13:52989400-53003400	Weak transcription	Spleen	Spleen
38	chr13:52989400-53015000	Weak transcription	Lung	lung
39	chr13:52990400-53002400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr13:52990400-53003000	Weak transcription	Brain Angular Gyrus	brain
41	chr13:52990600-53001400	Strong transcription	Osteobl	bone
42	chr13:52990800-53001600	Strong transcription	Fetal Intestine Small	intestine
43	chr13:52990800-53015000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
44	chr13:52991000-53000200	Strong transcription	Fetal Stomach	stomach
45	chr13:52991000-53007200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
46	chr13:52991200-53001400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr13:52991200-53017000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
48	chr13:52991400-52999600	Weak transcription	NHDF-Ad	bronchial
49	chr13:52991600-53008800	Weak transcription	Placenta Amnion	Placenta Amnion
50	chr13:52993200-53004400	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--

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