Variant report

Variant	nsv833616
Chromosome Location	chr18:29792336-29964212
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1970)
CpG islands
(count:61)
Chromatin interactive
region (count:68)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1970 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:29905267-29905422	HepG2	liver:	n/a	n/a
2	ARID3A	chr18:29962913-29963406	HepG2	liver:	n/a	n/a
3	ARID3A	chr18:29899090-29899515	HepG2	liver:	n/a	n/a
4	ARID3A	chr18:29851724-29851986	HepG2	liver:	n/a	n/a
5	ARID3A	chr18:29897304-29897515	HepG2	liver:	n/a	n/a
6	ARID3A	chr18:29958691-29958980	HepG2	liver:	n/a	n/a
7	ARID3A	chr18:29951929-29953042	HepG2	liver:	n/a	n/a
8	ARID3A	chr18:29869475-29869822	HepG2	liver:	n/a	n/a
9	ARID3A	chr18:29858231-29858695	HepG2	liver:	n/a	n/a
10	ARID3A	chr18:29957879-29958073	HepG2	liver:	n/a	n/a
11	ATF3	chr18:29929644-29930186	HCT-116	colon:	n/a	n/a
12	ATF3	chr18:29929779-29930125	A549	lung:	n/a	n/a
13	ATF3	chr18:29929626-29930236	HCT-116	colon:	n/a	n/a
14	ATF3	chr18:29897037-29897612	HCT-116	colon:	n/a	n/a
15	BACH1	chr18:29932272-29932282	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr18:29897394-29897429	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr18:29818854-29819068	H1-hESC	embryonic stem cell:	n/a	n/a
18	BATF	chr18:29881951-29882288	GM12878	blood:	n/a	n/a
19	BCL3	chr18:29962880-29963443	A549	lung:	n/a	n/a
20	BCL3	chr18:29951990-29952481	A549	lung:	n/a	n/a
21	BCL3	chr18:29962907-29963348	A549	lung:	n/a	n/a
22	BHLHE40	chr18:29860244-29860325	K562	blood:	n/a	chr18:29860277-29860286 chr18:29860275-29860288 chr18:29860276-29860285 chr18:29860277-29860286
23	BHLHE40	chr18:29963041-29963452	HepG2	liver:	n/a	n/a
24	BHLHE40	chr18:29952269-29952932	HepG2	liver:	n/a	n/a
25	BHLHE40	chr18:29958675-29958875	HepG2	liver:	n/a	n/a
26	BRCA1	chr18:29952055-29952893	Hela-S3	cervix:	n/a	n/a
27	CBX3	chr18:29952156-29953040	HCT-116	colon:	n/a	n/a
28	CBX3	chr18:29962857-29963623	HCT-116	colon:	n/a	n/a
29	CBX3	chr18:29962891-29963505	HCT-116	colon:	n/a	n/a
30	CBX3	chr18:29952044-29953084	HCT-116	colon:	n/a	n/a
31	CBX3	chr18:29929661-29930229	HCT-116	colon:	n/a	n/a
32	CEBPB	chr18:29897203-29897532	ECC-1	luminal epithelium:	n/a	chr18:29897318-29897329
33	CEBPB	chr18:29897198-29897455	HepG2	liver:	n/a	chr18:29897318-29897329
34	CEBPB	chr18:29897149-29897454	HepG2	liver:	n/a	chr18:29897318-29897329
35	CEBPB	chr18:29946477-29946963	ECC-1	luminal epithelium:	n/a	chr18:29946678-29946691 chr18:29946678-29946691
36	CEBPB	chr18:29858469-29858713	HepG2	liver:	n/a	n/a
37	CEBPB	chr18:29948185-29948484	HepG2	liver:	n/a	chr18:29948335-29948346
38	CEBPB	chr18:29829543-29829686	IMR90	lung:	n/a	n/a
39	CEBPB	chr18:29963083-29963413	HepG2	liver:	n/a	n/a
40	CEBPB	chr18:29962954-29963380	A549	lung:	n/a	n/a
41	CEBPB	chr18:29952459-29952886	HepG2	liver:	n/a	n/a
42	CEBPB	chr18:29951964-29953051	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr18:29897141-29897528	HepG2	liver:	n/a	chr18:29897318-29897329
44	CEBPB	chr18:29799742-29799841	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr18:29942471-29942861	MCF-7	breast:	n/a	chr18:29942612-29942629 chr18:29942827-29942838
46	CEBPB	chr18:29883347-29883682	HepG2	liver:	n/a	n/a
47	CEBPB	chr18:29940835-29941176	H1-hESC	embryonic stem cell:	n/a	chr18:29940914-29940925 chr18:29941121-29941134
48	CEBPB	chr18:29952077-29953161	HCT-116	colon:	n/a	n/a
49	CEBPB	chr18:29963034-29963400	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr18:29883349-29883685	IMR90	lung:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:29847791-29847841	AoSMC	blood vessel:	n/a
2	chr18:29847791-29847841	BJ	skin:	n/a
3	chr18:29847791-29847841	SAEC	small airway:	n/a
4	chr18:29847791-29847841	HCF	heart:	n/a
5	chr18:29847791-29847841	HPAEpiC	pulmonary alveolar:	n/a
6	chr18:29847791-29847841	NHDF-neo	bronchial:	n/a
7	chr18:29847791-29847841	NB4	blood:	n/a
8	chr18:29847791-29847841	CMK	blood:	n/a
9	chr18:29847791-29847841	HNPCEpiC	eye:	n/a
10	chr18:29847791-29847841	HEEpiC	esophagus:	n/a
11	chr18:29847791-29847841	GM19239	blood:	n/a
12	chr18:29847791-29847841	IMR90	lung:	fetal
13	chr18:29847791-29847841	HAEpiC	amniotic membrane:	n/a
14	chr18:29847791-29847841	ProgFib	skin:	n/a
15	chr18:29847791-29847841	ECC-1	luminal epithelium:	n/a
16	chr18:29847791-29847841	HCPEpiC	choroid plexus:	n/a
17	chr18:29847791-29847841	AG04449	skin:	fetal
18	chr18:29847791-29847841	GM12878	blood:	n/a
19	chr18:29847791-29847841	GM12891	blood:	n/a
20	chr18:29847791-29847841	PANC-1	pancreas:	n/a
21	chr18:29847791-29847841	MCF10A-Er-Src	breast:	n/a
22	chr18:29847791-29847841	PrEC	prostate:	n/a
23	chr18:29847791-29847841	HRPEpiC	eye:	n/a
24	chr18:29847791-29847841	HL-60	blood:	n/a
25	chr18:29847791-29847841	LNCaP	prostate:	n/a
26	chr18:29847791-29847841	Hepatocyte	liver:	n/a
27	chr18:29847791-29847841	AG09309	skin:	n/a
28	chr18:29847791-29847841	HEK293	kidney:	embryo
29	chr18:29847791-29847841	K562	blood:	n/a
30	chr18:29847791-29847841	ovcar-3	ovarian:	n/a
31	chr18:29847791-29847841	GM06990	blood:	n/a
32	chr18:29847791-29847841	RPTEC	kidney:	n/a
33	chr18:29847791-29847841	U87	brain:	n/a
34	chr18:29847791-29847841	HCT-116	colon:	n/a
35	chr18:29847791-29847841	Hela-S3	cervix:	n/a
36	chr18:29847791-29847841	HRE	kidney:	n/a
37	chr18:29847791-29847841	AG04450	lung:	fetal
38	chr18:29847791-29847841	PFSK-1	brain:	n/a
39	chr18:29847791-29847841	AG09319	gingival:	n/a
40	chr18:29847791-29847841	A549	lung:	n/a
41	chr18:29847791-29847841	SK-N-SH_RA	brain:	n/a
42	chr18:29847791-29847841	SKMC	muscle:	n/a
43	chr18:29847791-29847841	HUVEC	blood vessel:	n/a
44	chr18:29847791-29847841	Jurkat	blood:	n/a
45	chr18:29847791-29847841	NHBE	bronchial:	n/a
46	chr18:29847791-29847841	HepG2	liver:	n/a
47	chr18:29847791-29847841	GM12892	blood:	n/a
48	chr18:29847791-29847841	T-47D	breast:	n/a
49	chr18:29847791-29847841	NT2-D1	testis:	n/a
50	chr18:29847791-29847841	NH-A	brain:	n/a

(count:68 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr18:29960482..29963119-chr18:29963659..29966463,2	MCF-7	breast:
2	chr18:29940994..29943496-chr18:29945012..29946568,2	MCF-7	breast:
3	chr18:29854965..29857562-chr18:29891190..29893119,2	K562	blood:
4	chr18:29952934..29954642-chr18:29963321..29966112,2	MCF-7	breast:
5	chr18:29853249..29854777-chr18:29860158..29863062,2	K562	blood:
6	chr18:29942791..29945437-chr18:29947108..29948708,2	K562	blood:
7	chr18:29942732..29945838-chr18:30048998..30052033,3	MCF-7	breast:
8	chr18:29854965..29857562-chr18:29891190..29893119,2	K562	blood:
9	chr18:29913755..29914382-chr18:30048909..30049690,2	MCF-7	breast:
10	chr18:29948144..29949941-chr18:30049254..30052197,2	MCF-7	breast:
11	chr18:29847813..29851392-chr18:29854747..29858581,3	MCF-7	breast:
12	chr18:29895037..29897248-chr18:29897872..29900366,2	K562	blood:
13	chr18:29891994..29893877-chr18:29897571..29900006,2	MCF-7	breast:
14	chr18:29912040..29915183-chr18:29916652..29919648,4	MCF-7	breast:
15	chr18:29852094..29854619-chr18:29865481..29868899,3	K562	blood:
16	chr18:29869293..29870126-chr18:30132476..30133178,2	MCF-7	breast:
17	chr18:29887452..29890348-chr18:30046410..30049276,2	MCF-7	breast:
18	chr18:29915109..29917928-chr18:29952038..29954321,2	MCF-7	breast:
19	chr18:29952934..29954642-chr18:29963321..29966112,2	MCF-7	breast:
20	chr18:29940994..29943496-chr18:29945012..29946568,2	MCF-7	breast:
21	chr18:29936796..29939619-chr18:29941800..29943870,3	MCF-7	breast:
22	chr18:29896360..29897935-chr18:29901825..29904220,2	K562	blood:
23	chr18:29843865..29846147-chr18:30049369..30051018,2	MCF-7	breast:
24	chr18:29899850..29902793-chr18:29909603..29911236,2	MCF-7	breast:
25	chr18:29877540..29879536-chr18:29882707..29884848,2	MCF-7	breast:
26	chr18:29960482..29963119-chr18:29963659..29966463,2	MCF-7	breast:
27	chr18:29873261..29875337-chr18:30049350..30051070,2	MCF-7	breast:
28	chr18:29936796..29939619-chr18:29941800..29943870,3	MCF-7	breast:
29	chr18:29868718..29871349-chr18:30049265..30052223,3	MCF-7	breast:
30	chr18:29851552..29852413-chr18:30132133..30133147,4	MCF-7	breast:
31	chr18:29856972..29858473-chr18:30049654..30051815,2	MCF-7	breast:
32	chr18:29851378..29852356-chr18:30050569..30051553,4	MCF-7	breast:
33	chr18:29851742..29852316-chr18:30263045..30263644,2	MCF-7	breast:
34	chr18:29950469..29955579-chr18:30048383..30051595,6	MCF-7	breast:
35	chr18:29851628..29852386-chr18:30132192..30133063,2	MCF-7	breast:
36	chr18:29853249..29854777-chr18:29860158..29863062,2	K562	blood:
37	chr18:29930256..29933123-chr18:29933358..29935857,3	MCF-7	breast:
38	chr18:29899850..29902793-chr18:29909603..29911236,2	MCF-7	breast:
39	chr18:29952322..29955283-chr18:29962192..29964133,2	K562	blood:
40	chr18:29955010..29956616-chr18:29960394..29962375,2	MCF-7	breast:
41	chr18:29869178..29870066-chr18:30128854..30129812,2	MCF-7	breast:
42	chr18:29952322..29955283-chr18:29962192..29964133,2	K562	blood:
43	chr18:29869308..29870117-chr18:30050651..30051625,5	MCF-7	breast:
44	chr18:29851409..29852190-chr18:30050752..30051380,2	MCF-7	breast:
45	chr18:29877540..29879536-chr18:29882707..29884848,2	MCF-7	breast:
46	chr18:29931862..29933961-chr18:29952330..29954097,2	MCF-7	breast:
47	chr18:29851159..29852631-chr18:30128814..30129900,6	MCF-7	breast:
48	chr18:29891994..29893877-chr18:29897571..29900006,2	MCF-7	breast:
49	chr18:29867305..29869453-chr18:30048858..30050694,2	MCF-7	breast:
50	chr18:29837235..29838765-chr18:29839489..29841604,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MEP1B-3	chr18:29898404-29898738	NONHSAT058862
2	lnc-MEP1B-3	chr18:29891709-29891919	NONHSAT058862
3	lnc-FAM59A-1	chr18:29828719-29828995	ENSG00000263904.1
4	lnc-FAM59A-1	chr18:29825909-29826099	ENSG00000263904.1

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	FAM59A	hsa-miR-186-5p	chr18:29843701-29843695

Variant related genes	Relation type
GAREM	TF binding region
ENSG00000222395	TF binding region
ENSG00000264982	TF binding region
ENSG00000263904	TF binding region
GAREM	CpG island
ENSG00000222395	CpG island
ENSG00000264982	CpG island
ENSG00000263904	CpG island
ENSG00000092931	chromatin interactions
ENSG00000207556	chromatin interactions
ENSG00000264982	chromatin interactions
ENSG00000161547	chromatin interactions
ENSG00000141441	chromatin interactions

Extended variants
information (count: 5835 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:5835 , 50 per page) page: 1 2 3 4 5 6 7 ... 117

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs575480725	chr18:29792349-29792350	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs559345876	chr18:29792352-29792353	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs532781712	chr18:29792375-29792376	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs191872686	chr18:29792406-29792407	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs563237149	chr18:29792418-29792419	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs193095	chr18:29792485-29792486	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs117885240	chr18:29792530-29792531	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs568294889	chr18:29792558-29792559	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs535795200	chr18:29792566-29792567	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs184112723	chr18:29792675-29792676	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs550704262	chr18:29792677-29792678	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs540896488	chr18:29792716-29792717	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs7234401	chr18:29792796-29792797	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs370070075	chr18:29792811-29792812	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs569235401	chr18:29792825-29792826	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs558106250	chr18:29792860-29792861	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs188215064	chr18:29792871-29792872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs72939741	chr18:29792900-29792901	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs562575230	chr18:29792912-29792913	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs529774746	chr18:29792944-29792945	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs144892316	chr18:29792961-29792962	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs193160570	chr18:29793014-29793015	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs559394612	chr18:29793044-29793045	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs577818538	chr18:29793048-29793049	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs59381757	chr18:29793055-29793056	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs199858802	chr18:29793070-29793071	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs113156575	chr18:29793100-29793101	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs150721615	chr18:29793110-29793111	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs370173924	chr18:29793117-29793118	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs200671563	chr18:29793156-29793157	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs371904750	chr18:29793157-29793158	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs377435354	chr18:29793163-29793164	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs138989509	chr18:29793165-29793166	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs372147927	chr18:29793167-29793168	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs149917646	chr18:29793181-29793182	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs375895692	chr18:29793211-29793212	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs7238073	chr18:29793212-29793213	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs372197706	chr18:29793219-29793220	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs375226060	chr18:29793223-29793224	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs547923472	chr18:29793225-29793226	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs369048823	chr18:29793234-29793235	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs199912683	chr18:29793239-29793240	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs377012654	chr18:29793258-29793259	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs144943422	chr18:29793288-29793289	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs540092665	chr18:29793308-29793309	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs141050716	chr18:29793346-29793347	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs367637912	chr18:29793360-29793361	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs143349103	chr18:29793380-29793381	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs371428573	chr18:29793394-29793395	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs200135266	chr18:29793426-29793427	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

Disease	PMID	Source
Esophageal squamous carcinoma	18350619	CNVD
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
Glioblastoma multiforme	21922591	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
Lung cancer	18438408	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
Hepatocellular carcinoma	16750200	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
Breast cancer	17133270	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Colorectal cancer	16774939	CNVD
Colorectal cancer	21297112	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Glioblastoma multiforme	17002787	CNVD
Cancer	21183584	CNVD
Breast cancer	17603634	CNVD
Thyroid cancer	19087340	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Colorectal cancer	16912164	CNVD
Renal cell carcinoma	19150565	CNVD
Multiple myeloma	16616336	CNVD
Colorectal cancer	19150955	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	21811587	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2541 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:29784600-29795200	Enhancers	Fetal Intestine Large	intestine
2	chr18:29786800-29795200	Enhancers	Fetal Intestine Small	intestine
3	chr18:29788800-29793000	Weak transcription	HepG2	liver
4	chr18:29790400-29793200	Weak transcription	Duodenum Mucosa	Duodenum
5	chr18:29791200-29793200	Weak transcription	Liver	Liver
6	chr18:29791800-29793600	Weak transcription	Rectal Mucosa Donor 31	rectum
7	chr18:29793000-29794600	Enhancers	HepG2	liver
8	chr18:29793200-29794400	Enhancers	Duodenum Mucosa	Duodenum
9	chr18:29793200-29794600	Enhancers	Liver	Liver
10	chr18:29793600-29794200	Enhancers	Rectal Mucosa Donor 31	rectum
11	chr18:29795200-29796400	Weak transcription	Fetal Intestine Large	intestine
12	chr18:29795200-29799400	Weak transcription	Fetal Intestine Small	intestine
13	chr18:29796400-29796800	Enhancers	Fetal Intestine Large	intestine
14	chr18:29796800-29799400	Weak transcription	Fetal Intestine Large	intestine
15	chr18:29798600-29799000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr18:29799400-29800000	Enhancers	Fetal Intestine Small	intestine
17	chr18:29799400-29800200	Enhancers	Breast Myoepithelial Primary Cells	Breast
18	chr18:29799400-29800200	Enhancers	Fetal Intestine Large	intestine
19	chr18:29799600-29800000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr18:29813800-29814200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
21	chr18:29814200-29818400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr18:29814200-29819000	Enhancers	Fetal Intestine Large	intestine
23	chr18:29814600-29816800	Enhancers	Fetal Intestine Small	intestine
24	chr18:29814800-29815200	Enhancers	Pancreas	Pancrea
25	chr18:29815000-29815200	Enhancers	Duodenum Mucosa	Duodenum
26	chr18:29815200-29816200	Weak transcription	Duodenum Mucosa	Duodenum
27	chr18:29816000-29816200	Enhancers	Gastric	stomach
28	chr18:29816200-29816400	ZNF genes & repeats	Aorta	Aorta
29	chr18:29816200-29816800	Enhancers	Sigmoid Colon	Sigmoid Colon
30	chr18:29816200-29816800	Enhancers	Small Intestine	intestine
31	chr18:29816200-29817600	Enhancers	Duodenum Mucosa	Duodenum
32	chr18:29816200-29817600	Enhancers	Rectal Mucosa Donor 31	rectum
33	chr18:29816400-29818800	Weak transcription	Aorta	Aorta
34	chr18:29816800-29818000	Weak transcription	Fetal Intestine Small	intestine
35	chr18:29817600-29817800	Enhancers	Sigmoid Colon	Sigmoid Colon
36	chr18:29817600-29822200	Weak transcription	Rectal Mucosa Donor 31	rectum
37	chr18:29818000-29818800	Enhancers	Fetal Intestine Small	intestine
38	chr18:29818200-29819000	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr18:29818400-29818600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr18:29818400-29818800	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr18:29818400-29818800	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr18:29818400-29819000	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr18:29818400-29819000	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr18:29818600-29818800	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr18:29818600-29819000	Enhancers	H9 Cell Line	embryonic stem cell
46	chr18:29818600-29819000	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr18:29818600-29819000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr18:29818600-29819800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr18:29818800-29819000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr18:29818800-29819000	ZNF genes & repeats	Aorta	Aorta

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