Variant report

Variant	nsv1057722
Chromosome Location	chr18:45343965-45401360
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:397)
CpG islands
(count:61)
Chromatin interactive
region (count:29)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:5)

(count:397 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:45397603-45397941	HepG2	liver:	n/a	chr18:45397770-45397786
2	BACH1	chr18:45391890-45391917	K562	blood:	n/a	n/a
3	BATF	chr18:45379570-45379813	GM12878	blood:	n/a	n/a
4	BATF	chr18:45379443-45379821	GM12878	blood:	n/a	n/a
5	BCL11A	chr18:45379518-45379810	GM12878	blood:	n/a	n/a
6	BCL11A	chr18:45379557-45379920	GM12878	blood:	n/a	n/a
7	BHLHE40	chr18:45379541-45379905	HepG2	liver:	n/a	n/a
8	CEBPB	chr18:45370478-45370783	IMR90	lung:	n/a	chr18:45370610-45370619 chr18:45370608-45370621 chr18:45370610-45370619 chr18:45370610-45370619 chr18:45370610-45370621 chr18:45370608-45370619 chr18:45370610-45370619
9	CEBPB	chr18:45397656-45397855	HepG2	liver:	n/a	chr18:45397738-45397749
10	CEBPB	chr18:45389601-45389752	A549	lung:	n/a	n/a
11	CEBPB	chr18:45370495-45370786	HepG2	liver:	n/a	chr18:45370610-45370619 chr18:45370608-45370621 chr18:45370610-45370619 chr18:45370610-45370619 chr18:45370610-45370621 chr18:45370608-45370619 chr18:45370610-45370619
12	CEBPB	chr18:45379586-45379786	K562	blood:	n/a	n/a
13	CEBPB	chr18:45390727-45391043	IMR90	lung:	n/a	n/a
14	CEBPB	chr18:45390754-45391063	HepG2	liver:	n/a	n/a
15	CEBPB	chr18:45370450-45370801	K562	blood:	n/a	chr18:45370610-45370619 chr18:45370608-45370621 chr18:45370610-45370619 chr18:45370610-45370619 chr18:45370610-45370621 chr18:45370608-45370619 chr18:45370610-45370619
16	CEBPB	chr18:45370562-45370782	A549	lung:	n/a	chr18:45370610-45370619 chr18:45370608-45370621 chr18:45370610-45370619 chr18:45370610-45370619 chr18:45370610-45370621 chr18:45370608-45370619 chr18:45370610-45370619
17	CEBPB	chr18:45390790-45391041	A549	lung:	n/a	n/a
18	CEBPD	chr18:45379393-45379959	K562	blood:	n/a	n/a
19	CHD1	chr18:45380009-45380040	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr18:45397161-45397193	MCF-7	breast:	n/a	n/a
21	CTCF	chr18:45397100-45397250	HRPEpiC	eye:	n/a	n/a
22	CTCF	chr18:45399007-45399037	Spleen_OC	spleen:	n/a	n/a
23	CTCF	chr18:45391492-45391566	Lung_OC	lung:	n/a	n/a
24	CTCF	chr18:45391466-45391531	Medullo	brain:	n/a	n/a
25	CTCF	chr18:45379570-45379796	K562	blood:	n/a	n/a
26	CTCF	chr18:45397120-45397270	HPAF	blood vessel:	n/a	n/a
27	CTCF	chr18:45355382-45355441	LNCaP	prostate:	n/a	n/a
28	CTCF	chr18:45365660-45365810	K562	blood:	n/a	n/a
29	CTCF	chr18:45397000-45397150	HPAF	blood vessel:	n/a	n/a
30	CTCF	chr18:45397074-45397282	HUVEC	blood vessel:	n/a	n/a
31	CTCF	chr18:45391452-45391621	GM12878	blood:	n/a	n/a
32	CTCF	chr18:45391448-45391521	Pancreas_OC	pancreas:	n/a	n/a
33	CTCF	chr18:45391482-45391517	LNCaP	prostate:	n/a	n/a
34	CTCF	chr18:45397120-45397270	HEK293	kidney:	n/a	n/a
35	CTCF	chr18:45372789-45372882	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr18:45397147-45397225	GM12878	blood:	n/a	n/a
37	CTCF	chr18:45395363-45395424	Lung_OC	lung:	n/a	n/a
38	CTCF	chr18:45391400-45391550	HPAF	blood vessel:	n/a	n/a
39	CTCF	chr18:45370760-45370910	HL-60	blood:	n/a	n/a
40	CTCF	chr18:45397866-45397900	Fibrobl	skin:	n/a	n/a
41	CTCF	chr18:45379588-45379789	K562	blood:	n/a	n/a
42	CTCF	chr18:45397097-45397248	GM12878	blood:	n/a	n/a
43	CTCF	chr18:45365680-45365830	HEK293	kidney:	n/a	n/a
44	CTCF	chr18:45374240-45374390	HCM	heart:	n/a	n/a
45	CTCF	chr18:45355206-45355264	GM10248	blood:	n/a	n/a
46	CTCF	chr18:45397176-45397227	Medullo	brain:	n/a	n/a
47	CTCF	chr18:45391380-45391530	HCPEpiC	choroid plexus:	n/a	n/a
48	CTCF	chr18:45363960-45364110	RPTEC	kidney:	n/a	n/a
49	CTCF	chr18:45397102-45397279	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr18:45391400-45391550	HMEC	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:45364325-45364375	HCF	heart:	n/a
2	chr18:45364325-45364375	AG04450	lung:	fetal
3	chr18:45364325-45364375	MCF-7	breast:	n/a
4	chr18:45364325-45364375	SK-N-MC	brain:	n/a
5	chr18:45364325-45364375	AG09309	skin:	n/a
6	chr18:45364325-45364375	BJ	skin:	n/a
7	chr18:45364325-45364375	HRCEpiC	kidney:	n/a
8	chr18:45364325-45364375	AG10803	skin:	n/a
9	chr18:45364325-45364375	GM06990	blood:	n/a
10	chr18:45364325-45364375	H1-hESC	embryonic stem cell:	embryo
11	chr18:45364325-45364375	BE2_C	brain:	n/a
12	chr18:45364325-45364375	HL-60	blood:	n/a
13	chr18:45364325-45364375	HEEpiC	esophagus:	n/a
14	chr18:45364325-45364375	HCPEpiC	choroid plexus:	n/a
15	chr18:45364325-45364375	NHDF-neo	bronchial:	n/a
16	chr18:45364325-45364375	RPTEC	kidney:	n/a
17	chr18:45364325-45364375	SKMC	muscle:	n/a
18	chr18:45364325-45364375	HPAEpiC	pulmonary alveolar:	n/a
19	chr18:45364325-45364375	NB4	blood:	n/a
20	chr18:45364325-45364375	HEK293	kidney:	embryo
21	chr18:45364325-45364375	ProgFib	skin:	n/a
22	chr18:45364325-45364375	CMK	blood:	n/a
23	chr18:45364325-45364375	GM19239	blood:	n/a
24	chr18:45364325-45364375	MCF10A-Er-Src	breast:	n/a
25	chr18:45364325-45364375	HCT-116	colon:	n/a
26	chr18:45364325-45364375	Caco-2	colon:	n/a
27	chr18:45364325-45364375	NT2-D1	testis:	n/a
28	chr18:45364325-45364375	NH-A	brain:	n/a
29	chr18:45364325-45364375	AoSMC	blood vessel:	n/a
30	chr18:45364325-45364375	HNPCEpiC	eye:	n/a
31	chr18:45364325-45364375	SK-N-SH	brain:	n/a
32	chr18:45364325-45364375	ovcar-3	ovarian:	n/a
33	chr18:45364325-45364375	HepG2	liver:	n/a
34	chr18:45364325-45364375	PANC-1	pancreas:	n/a
35	chr18:45364325-45364375	HAEpiC	amniotic membrane:	n/a
36	chr18:45364325-45364375	PrEC	prostate:	n/a
37	chr18:45364325-45364375	HRE	kidney:	n/a
38	chr18:45364325-45364375	Hepatocyte	liver:	n/a
39	chr18:45364325-45364375	GM12878	blood:	n/a
40	chr18:45364325-45364375	HCM	heart:	n/a
41	chr18:45364325-45364375	AG04449	skin:	fetal
42	chr18:45364325-45364375	U87	brain:	n/a
43	chr18:45364325-45364375	T-47D	breast:	n/a
44	chr18:45364325-45364375	LNCaP	prostate:	n/a
45	chr18:45364325-45364375	PFSK-1	brain:	n/a
46	chr18:45364325-45364375	K562	blood:	n/a
47	chr18:45364325-45364375	ECC-1	luminal epithelium:	n/a
48	chr18:45364325-45364375	GM12891	blood:	n/a
49	chr18:45364325-45364375	HMEC	breast:	n/a
50	chr18:45364325-45364375	HUVEC	blood vessel:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:45388105..45390269-chr18:45393560..45395389,2	K562	blood:
2	chr18:45356981..45361316-chr18:45361915..45364794,4	K562	blood:
3	chr18:45356981..45360648-chr18:45361915..45364207,3	K562	blood:
4	chr18:45391818..45394321-chr18:45399787..45402085,2	MCF-7	breast:
5	chr18:45368468..45370509-chr18:45372236..45375671,3	K562	blood:
6	chr18:45367507..45370509-chr18:45371769..45374946,4	K562	blood:
7	chr18:45368468..45370509-chr18:45372236..45375671,3	K562	blood:
8	chr18:45401120..45404562-chr18:45404621..45407593,3	K562	blood:
9	chr18:45390223..45391741-chr18:45457289..45459666,2	MCF-7	breast:
10	chr18:45349020..45351185-chr18:45356009..45358662,2	K562	blood:
11	chr18:45393055..45395642-chr18:45402481..45404020,2	MCF-7	breast:
12	chr18:45396878..45399642-chr18:45401844..45403752,2	MCF-7	breast:
13	chr17:57916192..57918375-chr18:45387752..45390655,2	MCF-7	breast:
14	chr18:45400689..45404562-chr18:45404621..45407103,3	K562	blood:
15	chr18:45356981..45361316-chr18:45361915..45364794,4	K562	blood:
16	chr18:45370062..45371817-chr18:45453252..45455227,2	MCF-7	breast:
17	chr18:45367507..45370509-chr18:45371769..45374946,4	K562	blood:
18	chr18:45388105..45390269-chr18:45393560..45395389,2	K562	blood:
19	chr18:45355527..45357480-chr18:45358347..45361404,3	K562	blood:
20	chr18:45355527..45357480-chr18:45358347..45361404,3	K562	blood:
21	chr18:45349519..45352023-chr18:45354635..45356622,2	MCF-7	breast:
22	chr18:45372242..45375198-chr18:45455382..45457471,2	K562	blood:
23	chr18:45356981..45360648-chr18:45361915..45364207,3	K562	blood:
24	chr18:45367366..45369056-chr18:45455430..45458300,2	MCF-7	breast:
25	chr18:45349020..45351185-chr18:45356009..45358662,2	K562	blood:
26	chr18:45391818..45394321-chr18:45399787..45402085,2	MCF-7	breast:
27	chr16:2732028..2732807-chr18:45399145..45399845,2	Hela-S3	cervix:
28	chr18:45349519..45352023-chr18:45354635..45356622,2	MCF-7	breast:
29	chr18:45379137..45382377-chr18:45391896..45394821,3	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SMAD2-1	chr18:45346666-45352656	XLOC_012839
2	lnc-SMAD2-1	chr18:45355845-45356490	XLOC_012839
3	lnc-SMAD2-1	chr18:45350806-45351353	NONHSAT059172
4	lnc-ZBTB7C-5	chr18:45396844-45396935	NONHSAT059175

No data

(count:5 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	SMAD2	hsa-miR-155-5p	chr18:45359945-45359939
2	SMAD2	hsa-miR-200b-3p	chr18:45367863-45367857
3	SMAD2	hsa-miR-200a-3p	chr18:45371474-45371494
4	SMAD2	hsa-miR-324-5p	chr18:45359919-45359913
5	SMAD2	hsa-miR-155-5p	chr18:45359503-45359496

Variant related genes	Relation type
ENSG00000267541	TF binding region
ENSG00000267541	CpG island
ENSG00000267541	chromatin interactions
ENSG00000167977	chromatin interactions
ENSG00000175387	chromatin interactions

Extended variants
information (count: 2377 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:2377 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs574913840	chr18:45344082-45344083	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs562906960	chr18:45344094-45344095	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs140465200	chr18:45344098-45344099	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs114111824	chr18:45344111-45344112	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs565680517	chr18:45344142-45344143	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs554451278	chr18:45344225-45344226	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs370639621	chr18:45344310-45344311	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs186765441	chr18:45344349-45344350	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs540310347	chr18:45344415-45344416	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs192064019	chr18:45344424-45344425	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs548116324	chr18:45344450-45344451	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs374257577	chr18:45344492-45344493	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs145574739	chr18:45344567-45344568	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs557512281	chr18:45344582-45344583	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs114737949	chr18:45344591-45344592	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs539852415	chr18:45344697-45344698	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs12373324	chr18:45344790-45344791	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs183328367	chr18:45344855-45344856	Flanking Active TSS Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs188022393	chr18:45344857-45344858	Flanking Active TSS Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs542387914	chr18:45344885-45344886	Flanking Active TSS Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs374640169	chr18:45344891-45344892	Flanking Active TSS Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs149092053	chr18:45344923-45344924	Flanking Active TSS Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs189751757	chr18:45344952-45344953	Flanking Active TSS Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs151025629	chr18:45344961-45344962	Flanking Active TSS Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs543083030	chr18:45344964-45344965	Flanking Active TSS Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs563045374	chr18:45344981-45344982	Flanking Active TSS Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs577320489	chr18:45345010-45345011	Flanking Active TSS Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs546172240	chr18:45345012-45345013	Flanking Active TSS Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs182356452	chr18:45345020-45345021	Flanking Active TSS Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs563223599	chr18:45345062-45345063	Flanking Active TSS Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs559578583	chr18:45345079-45345080	Flanking Active TSS Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs528412789	chr18:45345092-45345093	Flanking Active TSS Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs548483221	chr18:45345213-45345214	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs532916173	chr18:45345295-45345296	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs568134377	chr18:45345301-45345302	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs115207556	chr18:45345306-45345307	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs188108781	chr18:45345316-45345317	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs143147346	chr18:45345318-45345319	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs570997854	chr18:45345320-45345321	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs539838571	chr18:45345371-45345372	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs4939632	chr18:45345393-45345394	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs148242868	chr18:45345401-45345402	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs62086501	chr18:45345402-45345403	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs556044045	chr18:45345439-45345440	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs147377953	chr18:45345451-45345452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs544409099	chr18:45345479-45345480	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs1792677	chr18:45345496-45345497	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs576559324	chr18:45345497-45345498	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs73953609	chr18:45345566-45345567	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs200045176	chr18:45345599-45345600	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
lymphocytic leukemia	21291569	CNVD
Barrett''s syndrome	19417022	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
18q deletion syndrome	19533772	CNVD
Acute myeloid leukemia	16864856	CNVD
Colorectal cancer	21102417	CNVD
Colorectal cancer	20709793	CNVD
Pancreatic cancer	21811562	CNVD
Basal cell lymphoma	21115979	CNVD
Mucosa-associated lymphoid tissue lymphomas	21459788	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
colon cancer	17210682	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	16573809	CNVD
Autism	16446308	CNVD
Colorectal cancer	19359472	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	18056178	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Metanephric adenoma	20802469	CNVD
small cell lung cancer	20016488	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Colorectal cancer	21297112	CNVD
Breast cancer	17603634	CNVD
Thyroid cancer	19087340	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Colorectal cancer	19150955	CNVD
Acute myeloid leukemia	21251322	CNVD
Colorectal cancer	16912164	CNVD
Lung cancer	18438408	CNVD
Seminomas	18059402	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
prenatal diagnosis	22389664	CNVD
Medulloblastoma	16783165	CNVD
Neuroblastoma	21508638	CNVD
Myelofibrosis	22110671	CNVD
Multiple myeloma	16461302	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Pilomyxoid astrocytoma	17436254	CNVD
Mental retardation	21062444	CNVD
Cancer	21183584	CNVD
Burkitt''s lymphoma	18698080	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Cancer	17160897	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Gastric cancer	16891809	CNVD
Idiopathic thrombocytopenic purpura	19566914	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16774939	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Asthma	20841430	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:1752 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:45327400-45358400	Weak transcription	HSMMtube	muscle
2	chr18:45327600-45352600	Weak transcription	Fetal Brain Female	brain
3	chr18:45328600-45351600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
4	chr18:45332200-45352400	Weak transcription	Adipose Nuclei	Adipose
5	chr18:45332600-45351800	Weak transcription	Fetal Muscle Leg	muscle
6	chr18:45332800-45351600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr18:45333000-45357200	Weak transcription	Primary hematopoietic stem cells	blood
8	chr18:45333200-45345600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr18:45333800-45351600	Weak transcription	A549	lung
10	chr18:45334600-45349800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
11	chr18:45335400-45365600	Weak transcription	Gastric	stomach
12	chr18:45335800-45351600	Weak transcription	Fetal Thymus	thymus
13	chr18:45336400-45351600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr18:45336600-45351600	Weak transcription	Thymus	Thymus
15	chr18:45337600-45357200	Weak transcription	Dnd41	blood
16	chr18:45339600-45359800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr18:45340200-45351800	Weak transcription	Fetal Muscle Trunk	muscle
18	chr18:45340400-45369400	Weak transcription	Fetal Stomach	stomach
19	chr18:45340600-45344000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr18:45340800-45347800	Weak transcription	Hela-S3	cervix
21	chr18:45341000-45364200	Weak transcription	Skeletal Muscle Female	skeletal muscle
22	chr18:45341400-45351800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
23	chr18:45342000-45344000	Enhancers	Breast Myoepithelial Primary Cells	Breast
24	chr18:45342000-45345400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr18:45342200-45344200	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr18:45342200-45344400	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr18:45342200-45344800	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr18:45342200-45345200	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr18:45342200-45384200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr18:45342400-45353800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr18:45342400-45365400	Weak transcription	Psoas Muscle	Psoas
32	chr18:45342600-45344200	Weak transcription	Rectal Smooth Muscle	rectum
33	chr18:45342600-45349200	Weak transcription	Primary T cells from cord blood	blood
34	chr18:45342600-45351600	Weak transcription	Left Ventricle	heart
35	chr18:45342800-45344000	Weak transcription	HUES64 Cell Line	embryonic stem cell
36	chr18:45343200-45344800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr18:45343200-45351600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr18:45343400-45344200	Weak transcription	H1 Cell Line	embryonic stem cell
39	chr18:45343400-45351800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr18:45343600-45344000	Flanking Active TSS	Ovary	ovary
41	chr18:45343600-45344200	Active TSS	NHLF	lung
42	chr18:45343600-45344400	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr18:45343600-45344400	Active TSS	Aorta	Aorta
44	chr18:45343600-45344600	Enhancers	H9 Cell Line	embryonic stem cell
45	chr18:45343600-45344600	Enhancers	Fetal Lung	lung
46	chr18:45343600-45345000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr18:45343600-45345000	Enhancers	Cortex derived primary cultured neurospheres	brain
48	chr18:45343600-45345000	Enhancers	Brain Germinal Matrix	brain
49	chr18:45343600-45345400	Enhancers	HUES6 Cell Line	embryonic stem cell
50	chr18:45343800-45344000	Enhancers	Pancreas	Pancrea

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