Variant report

Variant	esv1797261
Chromosome Location	chr13:52100949-52139113
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:462)
CpG islands
(count:123)
Chromatin interactive
region (count:35)
LncRNA
region (count:18)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:462 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:52107151-52107374	HepG2	liver:	n/a	n/a
2	ARID3A	chr13:52126155-52126435	K562	blood:	n/a	n/a
3	ARID3A	chr13:52115274-52115514	HepG2	liver:	n/a	n/a
4	ARID3A	chr13:52121568-52122179	HepG2	liver:	n/a	n/a
5	ATF2	chr13:52123121-52123651	GM12878	blood:	n/a	n/a
6	ATF2	chr13:52136132-52136782	GM12878	blood:	n/a	n/a
7	ATF2	chr13:52135931-52136861	GM12878	blood:	n/a	n/a
8	ATF3	chr13:52123195-52123525	K562	blood:	n/a	n/a
9	BACH1	chr13:52131701-52131754	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr13:52123216-52123576	GM12878	blood:	n/a	chr13:52123397-52123408 chr13:52123421-52123432
11	BATF	chr13:52123217-52123648	GM12878	blood:	n/a	chr13:52123397-52123408 chr13:52123421-52123432
12	BATF	chr13:52136405-52136818	GM12878	blood:	n/a	n/a
13	BATF	chr13:52136178-52136779	GM12878	blood:	n/a	n/a
14	BCL11A	chr13:52136238-52136591	GM12878	blood:	n/a	chr13:52136452-52136461
15	BCL11A	chr13:52123179-52123610	GM12878	blood:	n/a	n/a
16	BCL11A	chr13:52136292-52136718	GM12878	blood:	n/a	chr13:52136452-52136461
17	BCLAF1	chr13:52123189-52123582	GM12878	blood:	n/a	n/a
18	BCLAF1	chr13:52136158-52136809	GM12878	blood:	n/a	chr13:52136452-52136461
19	BHLHE40	chr13:52123242-52123624	K562	blood:	n/a	n/a
20	BHLHE40	chr13:52126175-52126488	K562	blood:	n/a	n/a
21	BHLHE40	chr13:52134067-52134933	GM12878	blood:	n/a	n/a
22	BHLHE40	chr13:52136102-52136841	GM12878	blood:	n/a	n/a
23	BHLHE40	chr13:52129347-52129443	K562	blood:	n/a	n/a
24	BHLHE40	chr13:52123350-52123741	HepG2	liver:	n/a	n/a
25	BHLHE40	chr13:52122976-52123063	HepG2	liver:	n/a	n/a
26	BRCA1	chr13:52131953-52132455	Hela-S3	cervix:	n/a	n/a
27	CCNT2	chr13:52116862-52117101	K562	blood:	n/a	n/a
28	CCNT2	chr13:52116007-52116475	K562	blood:	n/a	chr13:52116387-52116407
29	CCNT2	chr13:52123293-52123631	K562	blood:	n/a	n/a
30	CEBPB	chr13:52136012-52136929	GM12878	blood:	n/a	n/a
31	CEBPB	chr13:52131957-52132128	K562	blood:	n/a	chr13:52132076-52132087
32	CEBPB	chr13:52131895-52132279	A549	lung:	n/a	chr13:52132076-52132087
33	CEBPB	chr13:52131902-52132167	K562	blood:	n/a	chr13:52132076-52132087
34	CEBPB	chr13:52131895-52132261	HepG2	liver:	n/a	chr13:52132076-52132087
35	CEBPB	chr13:52131934-52132238	H1-hESC	embryonic stem cell:	n/a	chr13:52132076-52132087
36	CEBPB	chr13:52108254-52108862	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr13:52131859-52132298	A549	lung:	n/a	chr13:52132076-52132087
38	CEBPB	chr13:52127763-52127945	K562	blood:	n/a	n/a
39	CEBPB	chr13:52131811-52132701	Hela-S3	cervix:	n/a	chr13:52132076-52132087
40	CEBPB	chr13:52131998-52132134	HepG2	liver:	n/a	chr13:52132076-52132087
41	CEBPB	chr13:52131872-52132734	IMR90	lung:	n/a	chr13:52132076-52132087
42	CEBPB	chr13:52131855-52132354	A549	lung:	n/a	chr13:52132076-52132087
43	CEBPB	chr13:52131889-52132267	K562	blood:	n/a	chr13:52132076-52132087
44	CHD1	chr13:52136232-52136817	GM12878	blood:	n/a	n/a
45	CHD2	chr13:52108239-52108873	Hela-S3	cervix:	n/a	n/a
46	CHD2	chr13:52136086-52136585	GM12878	blood:	n/a	n/a
47	CHD2	chr13:52123289-52123479	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr13:52100940-52101090	HepG2	liver:	n/a	n/a
49	CTCF	chr13:52131800-52131950	HBMEC	blood vessel:	n/a	n/a
50	CTCF	chr13:52107877-52107971	GM20000	blood:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:52131904-52131954	U87	brain:	n/a
2	chr13:52131904-52131954	U87	brain:	n/a
3	chr13:52116184-52116234	HCM	heart:	n/a
4	chr13:52131904-52131954	AG04449	skin:	fetal
5	chr13:52131904-52131954	HRCEpiC	kidney:	n/a
6	chr13:52131904-52131954	K562	blood:	n/a
7	chr13:52131904-52131954	NB4	blood:	n/a
8	chr13:52116184-52116234	SAEC	small airway:	n/a
9	chr13:52116184-52116234	RPTEC	kidney:	n/a
10	chr13:52116184-52116234	PFSK-1	brain:	n/a
11	chr13:52116184-52116234	HRPEpiC	eye:	n/a
12	chr13:52131904-52131954	Hela-S3	cervix:	n/a
13	chr13:52116184-52116234	HNPCEpiC	eye:	n/a
14	chr13:52131904-52131954	GM06990	blood:	n/a
15	chr13:52131904-52131954	ovcar-3	ovarian:	n/a
16	chr13:52116184-52116234	Hepatocyte	liver:	n/a
17	chr13:52116184-52116234	NT2-D1	testis:	n/a
18	chr13:52116184-52116234	NHDF-neo	bronchial:	n/a
19	chr13:52116184-52116234	A549	lung:	n/a
20	chr13:52131904-52131954	HL-60	blood:	n/a
21	chr13:52131904-52131954	HPAEpiC	pulmonary alveolar:	n/a
22	chr13:52131904-52131954	PrEC	prostate:	n/a
23	chr13:52131904-52131954	AG04450	lung:	fetal
24	chr13:52116184-52116234	CMK	blood:	n/a
25	chr13:52116184-52116234	GM06990	blood:	n/a
26	chr13:52131904-52131954	GM19239	blood:	n/a
27	chr13:52116184-52116234	AG09309	skin:	n/a
28	chr13:52116184-52116234	HMEC	breast:	n/a
29	chr13:52131904-52131954	NT2-D1	testis:	n/a
30	chr13:52131904-52131954	H1-hESC	embryonic stem cell:	embryo
31	chr13:52131904-52131954	HIPEpiC	eye:	n/a
32	chr13:52116184-52116234	AoSMC	blood vessel:	n/a
33	chr13:52116184-52116234	HCF	heart:	n/a
34	chr13:52116184-52116234	Jurkat	blood:	n/a
35	chr13:52116184-52116234	MCF-7	breast:	n/a
36	chr13:52131904-52131954	SK-N-MC	brain:	n/a
37	chr13:52116184-52116234	ProgFib	skin:	n/a
38	chr13:52116184-52116234	GM12891	blood:	n/a
39	chr13:52116184-52116234	HEK293	kidney:	embryo
40	chr13:52131904-52131954	AG09319	gingival:	n/a
41	chr13:52116184-52116234	ovcar-3	ovarian:	n/a
42	chr13:52131904-52131954	ECC-1	luminal epithelium:	n/a
43	chr13:52116184-52116234	NH-A	brain:	n/a
44	chr13:52116184-52116234	HepG2	liver:	n/a
45	chr13:52116184-52116234	PANC-1	pancreas:	n/a
46	chr13:52131904-52131954	HCT-116	colon:	n/a
47	chr13:52131904-52131954	A549	lung:	n/a
48	chr13:52116184-52116234	HUVEC	blood vessel:	n/a
49	chr13:52131904-52131954	PANC-1	pancreas:	n/a
50	chr13:52131904-52131954	HCPEpiC	choroid plexus:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:52025558..52028452-chr13:52109917..52111699,2	MCF-7	breast:
2	chr13:52124143..52125807-chr13:52127264..52129826,2	K562	blood:
3	chr13:52126960..52128462-chr13:52130679..52132908,2	MCF-7	breast:
4	chr13:52097892..52100856-chr13:52116371..52118761,2	MCF-7	breast:
5	chr13:52025813..52028361-chr13:52135835..52138227,3	K562	blood:
6	chr13:52132543..52134080-chr13:52136895..52139620,2	MCF-7	breast:
7	chr13:52025591..52028718-chr13:52111998..52119680,9	MCF-7	breast:
8	chr13:52124143..52125807-chr13:52127264..52129826,2	K562	blood:
9	chr13:52024743..52028940-chr13:52112359..52118516,11	MCF-7	breast:
10	chr13:52131962..52135088-chr13:52156352..52158320,3	MCF-7	breast:
11	chr13:52026832..52028649-chr13:52125525..52127655,3	MCF-7	breast:
12	chr13:52107547..52108389-chr6:31782522..31783093,2	Hela-S3	cervix:
13	chr13:52026677..52028551-chr13:52122962..52125114,3	K562	blood:
14	chr13:52108221..52111487-chr13:52112339..52115268,3	K562	blood:
15	chr13:52112849..52115667-chr13:52128292..52129894,2	MCF-7	breast:
16	chr13:52025248..52027565-chr13:52113097..52117557,5	K562	blood:
17	chr13:52114829..52118630-chr13:52158674..52160777,3	MCF-7	breast:
18	chr13:52122493..52124445-chr13:52397766..52400689,2	K562	blood:
19	chr13:52023304..52026235-chr13:52130476..52133449,3	MCF-7	breast:
20	chr13:52112849..52115667-chr13:52128292..52129894,2	MCF-7	breast:
21	chr13:52122039..52124895-chr13:52125029..52128951,4	MCF-7	breast:
22	chr13:52097331..52099871-chr13:52124586..52126544,2	MCF-7	breast:
23	chr13:52026353..52029018-chr13:52131265..52135290,3	MCF-7	breast:
24	chr13:52105659..52107581-chr13:52114621..52118462,3	MCF-7	breast:
25	chr13:52096223..52098756-chr13:52108625..52111484,2	MCF-7	breast:
26	chr13:52024180..52026043-chr13:52139073..52141757,2	K562	blood:
27	chr13:52125996..52128858-chr13:52157695..52159658,2	MCF-7	breast:
28	chr13:52025527..52027084-chr13:52138971..52141023,2	MCF-7	breast:
29	chr13:52108221..52111487-chr13:52112339..52115268,3	K562	blood:
30	chr13:52026308..52028384-chr13:52105731..52108665,3	MCF-7	breast:
31	chr13:52126960..52128462-chr13:52130679..52132908,2	MCF-7	breast:
32	chr13:52024780..52027941-chr13:52120513..52124566,4	MCF-7	breast:
33	chr13:52093719..52095925-chr13:52134002..52136713,2	MCF-7	breast:
34	chr13:52024546..52028811-chr13:52131702..52137649,7	MCF-7	breast:
35	chr13:52025248..52026911-chr13:52113097..52115719,3	K562	blood:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WDFY2-2	chr13:52123846-52124299	ENSG00000236778.3
2	lnc-WDFY2-2	chr13:52123846-52123938	ENSG00000236778.3
3	lnc-WDFY2-2	chr13:52115694-52116320	ENSG00000236778.3
4	lnc-WDFY2-2	chr13:52125261-52125324	ENSG00000236778.3
5	lnc-WDFY2-2	chr13:52123846-52124042	ENSG00000236778.3
6	lnc-WDFY2-2	chr13:52123255-52123366	ENSG00000236778.3
7	lnc-WDFY2-2	chr13:52126219-52126471	ENSG00000236778.3
8	lnc-WDFY2-2	chr13:52123846-52124042	ENSG00000236778.3
9	lnc-WDFY2-2	chr13:52123846-52124028	ENSG00000236778.3
10	lnc-WDFY2-2	chr13:52126219-52126500	ENSG00000236778.3
11	lnc-WDFY2-2	chr13:52123846-52124028	ENSG00000236778.3
12	lnc-WDFY2-2	chr13:52123846-52124028	ENSG00000236778.3
13	lnc-WDFY2-2	chr13:52123846-52124011	ENSG00000236778.3
14	lnc-WDFY2-2	chr13:52123255-52123366	ENSG00000236778.3
15	lnc-WDFY2-2	chr13:52123846-52123890	ENSG00000236778.3
16	lnc-WDFY2-2	chr13:52115694-52116320	ENSG00000236778.3
17	lnc-WDFY2-2	chr13:52123846-52124128	ENSG00000236778
18	lnc-WDFY2-2	chr13:52116061-52116321	ENSG00000236778.3

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4703-3p	chr13:52126773-52126794	MIMAT0019802
hsa-miR-4703-5p	chr13:52126735-52126757	MIMAT0019801

No data

Variant related genes	Relation type
INTS6-AS1	TF binding region
MIR4703	TF binding region
RNU6-65P	TF binding region
INTS6-AS1	CpG island
MIR4703	CpG island
RNU6-65P	CpG island
ENSG00000139668	chromatin interactions
ENSG00000224892	chromatin interactions
ENSG00000102786	chromatin interactions
ENSG00000266611	chromatin interactions
ENSG00000236778	chromatin interactions
ENSG00000204390	chromatin interactions
ENSG00000206920	chromatin interactions
ENSG00000252141	chromatin interactions

Extended variants
information (count: 1354 )
Associated
traits (count: 121 )

Variant overlapped rSNPs/rCNVs (count:1354 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17075764	chr13:52100949-52100950	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs558509314	chr13:52100957-52100958	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs368831406	chr13:52100972-52100973	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs548071493	chr13:52100986-52100987	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs567822461	chr13:52101005-52101006	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs138488278	chr13:52101018-52101019	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs181803868	chr13:52101069-52101070	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs9568623	chr13:52101076-52101077	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs141335800	chr13:52101095-52101096	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs537971902	chr13:52101168-52101169	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs557561634	chr13:52101170-52101171	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs577818356	chr13:52101174-52101175	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs186317848	chr13:52101178-52101179	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs191165667	chr13:52101188-52101189	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs143872804	chr13:52101201-52101202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs542635505	chr13:52101255-52101256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs375344718	chr13:52101256-52101257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs554149828	chr13:52101268-52101269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs562570738	chr13:52101277-52101278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs574006794	chr13:52101287-52101288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs537864154	chr13:52101331-52101332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs201222726	chr13:52101375-52101376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs561129442	chr13:52101381-52101382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs545144417	chr13:52101396-52101397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs374878869	chr13:52101420-52101421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs138685103	chr13:52101492-52101493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs547639672	chr13:52101493-52101494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs562885459	chr13:52101537-52101538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs369953163	chr13:52101570-52101571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs530443477	chr13:52101626-52101627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs555945575	chr13:52101643-52101644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs142877977	chr13:52101697-52101698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs568909901	chr13:52101746-52101747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs118071860	chr13:52101750-52101751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs545648109	chr13:52101751-52101752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs551462412	chr13:52101764-52101765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs571216969	chr13:52101778-52101779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs534008852	chr13:52101791-52101792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs114636496	chr13:52101802-52101803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs573480566	chr13:52101819-52101820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs565552520	chr13:52101832-52101833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs536176691	chr13:52101855-52101856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs139787357	chr13:52101892-52101893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs75484853	chr13:52101904-52101905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs545033355	chr13:52101993-52101994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs565393401	chr13:52102013-52102014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs572419479	chr13:52102044-52102045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs560942981	chr13:52102053-52102054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs369937791	chr13:52102054-52102055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs182176435	chr13:52102064-52102065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:121)

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
Trisomy	24170809	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
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
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
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
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
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21990379	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Gastric cancer	17908304	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Schizophrenia	23813976	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:52097600-52108600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr13:52098200-52101000	Enhancers	HepG2	liver
3	chr13:52098200-52106800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr13:52098800-52101000	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr13:52098800-52106800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr13:52099000-52101000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr13:52099800-52106400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
8	chr13:52099800-52107000	Weak transcription	HMEC	breast
9	chr13:52100000-52101200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr13:52100200-52107000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr13:52100200-52113800	Weak transcription	NHDF-Ad	bronchial
12	chr13:52100600-52106800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr13:52100600-52113000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr13:52100800-52107000	Weak transcription	A549	lung
15	chr13:52101000-52106800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
16	chr13:52101000-52106800	Weak transcription	HepG2	liver
17	chr13:52101200-52107000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr13:52106400-52110000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
19	chr13:52106600-52108200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
20	chr13:52106600-52109400	Enhancers	Hela-S3	cervix
21	chr13:52106600-52109600	Enhancers	Primary T cells from cord blood	blood
22	chr13:52106800-52107000	Weak transcription	NHEK	skin
23	chr13:52106800-52107200	Enhancers	H1 Cell Line	embryonic stem cell
24	chr13:52106800-52107200	Enhancers	H9 Cell Line	embryonic stem cell
25	chr13:52106800-52107200	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr13:52106800-52107200	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr13:52106800-52107200	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr13:52106800-52107200	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr13:52106800-52107200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr13:52106800-52107200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr13:52106800-52107200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr13:52106800-52107400	Enhancers	Muscle Satellite Cultured Cells	--
33	chr13:52106800-52107400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr13:52106800-52107600	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr13:52106800-52108000	Enhancers	Monocytes-CD14+_RO01746	blood
36	chr13:52106800-52108200	Enhancers	Primary neutrophils fromperipheralblood	blood
37	chr13:52106800-52108200	Enhancers	Primary hematopoietic stem cells short term culture	blood
38	chr13:52106800-52108400	Enhancers	Primary T helper cells PMA-I stimulated	--
39	chr13:52106800-52108400	Enhancers	HepG2	liver
40	chr13:52106800-52108600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr13:52106800-52109400	Enhancers	Primary T killer memory cells from peripheral blood	blood
42	chr13:52106800-52109600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
43	chr13:52106800-52109600	Enhancers	Primary T helper naive cells from peripheral blood	blood
44	chr13:52106800-52109600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
45	chr13:52106800-52109600	Enhancers	Primary T helper cells fromperipheralblood	blood
46	chr13:52106800-52109600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
47	chr13:52106800-52110000	Enhancers	Primary monocytes fromperipheralblood	blood
48	chr13:52107000-52107200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
49	chr13:52107000-52107200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr13:52107000-52107200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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