Variant report

Variant	nsv2277
Chromosome Location	chr18:43543715-43588579
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:848)
CpG islands
(count:855)
Chromatin interactive
region (count:19)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:848 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:43547067-43547601	HepG2	liver:	n/a	n/a
2	ARID3A	chr18:43547271-43547530	K562	blood:	n/a	n/a
3	ARID3A	chr18:43554133-43554483	HepG2	liver:	n/a	n/a
4	ARID3A	chr18:43554131-43554486	K562	blood:	n/a	n/a
5	ATF1	chr18:43578215-43578534	K562	blood:	n/a	n/a
6	ATF2	chr18:43547052-43547554	GM12878	blood:	n/a	chr18:43547216-43547230
7	ATF3	chr18:43547202-43547470	K562	blood:	n/a	chr18:43547402-43547411 chr18:43547289-43547298
8	ATF3	chr18:43547146-43547404	K562	blood:	n/a	chr18:43547289-43547298
9	ATF3	chr18:43547151-43547412	HepG2	liver:	n/a	chr18:43547402-43547411 chr18:43547289-43547298
10	ATF3	chr18:43558087-43558316	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr18:43558103-43558359	GM12878	blood:	n/a	chr18:43558209-43558220
12	BCL3	chr18:43563538-43563896	GM12878	blood:	n/a	n/a
13	BHLHE40	chr18:43557689-43557726	GM12878	blood:	n/a	n/a
14	BHLHE40	chr18:43546956-43547568	HepG2	liver:	n/a	n/a
15	BHLHE40	chr18:43547082-43547484	K562	blood:	n/a	n/a
16	BHLHE40	chr18:43554153-43554442	K562	blood:	n/a	n/a
17	BHLHE40	chr18:43554090-43554382	GM12878	blood:	n/a	n/a
18	BHLHE40	chr18:43547126-43547638	GM12878	blood:	n/a	n/a
19	BRCA1	chr18:43547511-43547695	H1-hESC	embryonic stem cell:	n/a	n/a
20	BRCA1	chr18:43562978-43563020	HepG2	liver:	n/a	n/a
21	BRCA1	chr18:43547169-43547446	Hela-S3	cervix:	n/a	n/a
22	CBX3	chr18:43581884-43582222	K562	blood:	n/a	n/a
23	CBX3	chr18:43569233-43569505	K562	blood:	n/a	n/a
24	CBX3	chr18:43581824-43582245	K562	blood:	n/a	n/a
25	CBX3	chr18:43547044-43547492	K562	blood:	n/a	n/a
26	CCNT2	chr18:43578235-43578585	K562	blood:	n/a	n/a
27	CCNT2	chr18:43547035-43547689	K562	blood:	n/a	chr18:43547427-43547436
28	CEBPB	chr18:43547169-43547566	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr18:43557998-43558441	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr18:43554099-43554562	IMR90	lung:	n/a	chr18:43554374-43554387 chr18:43554337-43554348
31	CEBPB	chr18:43558190-43558374	HepG2	liver:	n/a	n/a
32	CEBPB	chr18:43554165-43554526	H1-hESC	embryonic stem cell:	n/a	chr18:43554374-43554387 chr18:43554337-43554348
33	CEBPB	chr18:43554135-43554521	K562	blood:	n/a	chr18:43554374-43554387 chr18:43554337-43554348
34	CEBPB	chr18:43546843-43547477	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr18:43554127-43554559	A549	lung:	n/a	chr18:43554374-43554387 chr18:43554337-43554348
36	CEBPB	chr18:43579704-43580305	HepG2	liver:	n/a	n/a
37	CEBPB	chr18:43580017-43580281	IMR90	lung:	n/a	n/a
38	CEBPB	chr18:43554187-43554548	HepG2	liver:	n/a	chr18:43554374-43554387 chr18:43554337-43554348
39	CEBPB	chr18:43554102-43554549	Hela-S3	cervix:	n/a	chr18:43554374-43554387 chr18:43554337-43554348
40	CEBPB	chr18:43578317-43578516	K562	blood:	n/a	n/a
41	CEBPB	chr18:43573323-43573873	IMR90	lung:	n/a	n/a
42	CEBPB	chr18:43547220-43547420	HepG2	liver:	n/a	n/a
43	CEBPB	chr18:43573347-43573749	Hela-S3	cervix:	n/a	n/a
44	CHD1	chr18:43554128-43554232	GM12878	blood:	n/a	n/a
45	CHD1	chr18:43546831-43547346	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD1	chr18:43547005-43547932	GM12878	blood:	n/a	n/a
47	CHD2	chr18:43546667-43547619	Hela-S3	cervix:	n/a	n/a
48	CHD2	chr18:43547055-43547458	K562	blood:	n/a	n/a
49	CHD2	chr18:43546668-43547531	GM12878	blood:	n/a	n/a
50	CHD2	chr18:43546993-43547685	HepG2	liver:	n/a	n/a

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:43551416-43551466	GM06990	blood:	n/a
2	chr18:43551416-43551466	GM06990	blood:	n/a
3	chr18:43547252-43547302	Jurkat	blood:	n/a
4	chr18:43546845-43546895	NB4	blood:	n/a
5	chr18:43547356-43547406	SAEC	small airway:	n/a
6	chr18:43547356-43547406	AG09319	gingival:	n/a
7	chr18:43547806-43547856	SK-N-MC	brain:	n/a
8	chr18:43545025-43545075	HCT-116	colon:	n/a
9	chr18:43547177-43547227	ECC-1	luminal epithelium:	n/a
10	chr18:43547356-43547406	IMR90	lung:	fetal
11	chr18:43567084-43567134	SKMC	muscle:	n/a
12	chr18:43548144-43548194	ProgFib	skin:	n/a
13	chr18:43546845-43546895	HEEpiC	esophagus:	n/a
14	chr18:43547530-43547580	AG09319	gingival:	n/a
15	chr18:43551416-43551466	AG10803	skin:	n/a
16	chr18:43547806-43547856	HCM	heart:	n/a
17	chr18:43547338-43547388	Hepatocyte	liver:	n/a
18	chr18:43545025-43545075	HCM	heart:	n/a
19	chr18:43546845-43546895	HUVEC	blood vessel:	n/a
20	chr18:43547252-43547302	HL-60	blood:	n/a
21	chr18:43547356-43547406	K562	blood:	n/a
22	chr18:43567084-43567134	NHBE	bronchial:	n/a
23	chr18:43547351-43547401	HL-60	blood:	n/a
24	chr18:43547252-43547302	HUVEC	blood vessel:	n/a
25	chr18:43567084-43567134	HCM	heart:	n/a
26	chr18:43547806-43547856	Caco-2	colon:	n/a
27	chr18:43547701-43547751	HL-60	blood:	n/a
28	chr18:43545025-43545075	HRPEpiC	eye:	n/a
29	chr18:43547356-43547406	Hepatocyte	liver:	n/a
30	chr18:43547177-43547227	AG10803	skin:	n/a
31	chr18:43547356-43547406	CMK	blood:	n/a
32	chr18:43567084-43567134	NB4	blood:	n/a
33	chr18:43547335-43547385	HIPEpiC	eye:	n/a
34	chr18:43547338-43547388	SK-N-SH_RA	brain:	n/a
35	chr18:43545025-43545075	HepG2	liver:	n/a
36	chr18:43545025-43545075	Caco-2	colon:	n/a
37	chr18:43547338-43547388	BJ	skin:	n/a
38	chr18:43546845-43546895	HEK293	kidney:	embryo
39	chr18:43551416-43551466	HEEpiC	esophagus:	n/a
40	chr18:43545025-43545075	HIPEpiC	eye:	n/a
41	chr18:43547351-43547401	GM12878	blood:	n/a
42	chr18:43545025-43545075	NH-A	brain:	n/a
43	chr18:43547530-43547580	HNPCEpiC	eye:	n/a
44	chr18:43567084-43567134	HMEC	breast:	n/a
45	chr18:43548144-43548194	HCT-116	colon:	n/a
46	chr18:43547806-43547856	HEEpiC	esophagus:	n/a
47	chr18:43546845-43546895	AG04450	lung:	fetal
48	chr18:43547335-43547385	T-47D	breast:	n/a
49	chr18:43547806-43547856	HCPEpiC	choroid plexus:	n/a
50	chr18:43547338-43547388	HCPEpiC	choroid plexus:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:43578639..43580570-chr18:43582338..43584371,2	MCF-7	breast:
2	chr18:43504494..43505026-chr18:43554152..43554693,2	MCF-7	breast:
3	chr18:43572012..43574368-chr18:43575627..43577632,2	K562	blood:
4	chr18:43578639..43580570-chr18:43582338..43584371,2	MCF-7	breast:
5	chr18:43580506..43582779-chr18:43587364..43589939,2	K562	blood:
6	chr18:43548996..43552453-chr18:43650910..43654147,4	MCF-7	breast:
7	chr18:43545858..43548536-chr18:43676652..43678402,2	MCF-7	breast:
8	chr18:43578214..43579999-chr18:43649262..43651951,2	K562	blood:
9	chr18:43553938..43554665-chr18:43653434..43654381,2	MCF-7	breast:
10	chr18:43580716..43582929-chr18:43614441..43616520,2	K562	blood:
11	chr18:43567575..43569342-chr18:43570587..43572226,2	MCF-7	breast:
12	chr18:43580506..43582779-chr18:43587364..43589939,2	K562	blood:
13	chr18:43553826..43554616-chr18:43653485..43654035,3	MCF-7	breast:
14	chr18:43245206..43245747-chr18:43553737..43554546,2	K562	blood:
15	chr18:43200584..43201546-chr18:43553704..43554682,3	K562	blood:
16	chr18:43577618..43580480-chr18:43580513..43583485,2	K562	blood:
17	chr18:43577618..43580480-chr18:43580513..43583485,2	K562	blood:
18	chr18:43578212..43579999-chr18:43649262..43652409,3	K562	blood:
19	chr18:43567575..43569342-chr18:43570587..43572226,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EPG5-3	chr18:43569619-43569911	NONHSAT059121

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	PSTPIP2	hsa-miR-24-3p	chr18:43565076-43565101
2	PSTPIP2	hsa-miR-24-3p	chr18:43564835-43564858

Variant related genes	Relation type
EPG5	TF binding region
PSTPIP2	TF binding region
RN7SKP26	TF binding region
EPG5	CpG island
PSTPIP2	CpG island
RN7SKP26	CpG island
ENSG00000152234	chromatin interactions
ENSG00000152229	chromatin interactions

Extended variants
information (count: 1747 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:1747 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs187235341	chr18:43543838-43543839	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs191893671	chr18:43543845-43543846	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs7231179	chr18:43543864-43543865	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs184086417	chr18:43543907-43543908	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs540386100	chr18:43543908-43543909	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs551687689	chr18:43543963-43543964	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs373604848	chr18:43543973-43543974	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs79232325	chr18:43543997-43543998	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs386802857	chr18:43544018-43544019	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs572633687	chr18:43544019-43544020	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs539841613	chr18:43544020-43544021	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs565124204	chr18:43544037-43544038	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs189650861	chr18:43544061-43544062	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs71358416	chr18:43544072-43544073	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs142028617	chr18:43544081-43544082	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs371483411	chr18:43544123-43544124	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs147973084	chr18:43544157-43544158	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs531053446	chr18:43544159-43544160	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs116740613	chr18:43544175-43544176	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs531117583	chr18:43544193-43544194	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs114359775	chr18:43544205-43544206	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs570953183	chr18:43544230-43544231	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs7235629	chr18:43544236-43544237	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs546974633	chr18:43544327-43544328	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs568466475	chr18:43544355-43544356	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs535357542	chr18:43544399-43544400	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs557235560	chr18:43544437-43544438	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs373650644	chr18:43544463-43544464	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs192287559	chr18:43544508-43544509	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs539600658	chr18:43544518-43544519	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs115462943	chr18:43544521-43544522	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs572597221	chr18:43544523-43544524	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs539950703	chr18:43544536-43544537	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs376956505	chr18:43544540-43544541	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs114190282	chr18:43544576-43544577	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs529751295	chr18:43544619-43544620	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs569738912	chr18:43544676-43544677	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs531647915	chr18:43544700-43544701	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs542124374	chr18:43544788-43544789	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs563985764	chr18:43544793-43544794	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs146121727	chr18:43544840-43544841	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs546409231	chr18:43544848-43544849	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs140143499	chr18:43544872-43544873	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs201842565	chr18:43544874-43544875	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs371142827	chr18:43544875-43544876	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs142023125	chr18:43544876-43544877	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs116571987	chr18:43544967-43544968	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs529274509	chr18:43545017-43545018	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs535070561	chr18:43545024-43545025	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs373689243	chr18:43545026-43545027	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

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
low-grade B-cell lymphoma tumor	18367492	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
Breast cancer	21364760	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Prostate cancer	22341455	CNVD
Congenital anomalies of the kidney and urinary tract	18852474	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
Breast cancer	22522925	CNVD

Chromatin state (count:1149 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:43492400-43546600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr18:43494000-43546600	Weak transcription	Stomach Mucosa	stomach
3	chr18:43519200-43546600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr18:43529000-43546400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr18:43534200-43545600	Weak transcription	Fetal Brain Male	brain
6	chr18:43534600-43546600	Weak transcription	Gastric	stomach
7	chr18:43535000-43546400	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr18:43535000-43546400	Weak transcription	GM12878-XiMat	blood
9	chr18:43535200-43545200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr18:43535200-43545200	Weak transcription	Brain Hippocampus Middle	brain
11	chr18:43535200-43545200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr18:43535200-43545400	Weak transcription	Brain Angular Gyrus	brain
13	chr18:43535200-43545600	Weak transcription	Brain Germinal Matrix	brain
14	chr18:43535200-43545600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr18:43535200-43545600	Weak transcription	Small Intestine	intestine
16	chr18:43535200-43546000	Weak transcription	Fetal Intestine Small	intestine
17	chr18:43535200-43546200	Weak transcription	HUVEC	blood vessel
18	chr18:43535200-43546400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr18:43535200-43546400	Weak transcription	Colon Smooth Muscle	Colon
20	chr18:43535200-43546400	Weak transcription	Fetal Muscle Trunk	muscle
21	chr18:43535200-43546400	Weak transcription	Fetal Stomach	stomach
22	chr18:43535200-43546400	Weak transcription	Rectal Smooth Muscle	rectum
23	chr18:43535200-43546600	Weak transcription	Spleen	Spleen
24	chr18:43535400-43545000	Weak transcription	Brain Inferior Temporal Lobe	brain
25	chr18:43535400-43545600	Weak transcription	Hela-S3	cervix
26	chr18:43535400-43545800	Weak transcription	Stomach Smooth Muscle	stomach
27	chr18:43535400-43546200	Weak transcription	Cortex derived primary cultured neurospheres	brain
28	chr18:43535400-43546400	Weak transcription	HUES6 Cell Line	embryonic stem cell
29	chr18:43535400-43546400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr18:43535400-43546400	Weak transcription	Brain Anterior Caudate	brain
31	chr18:43535400-43546400	Weak transcription	Brain Cingulate Gyrus	brain
32	chr18:43535400-43546400	Weak transcription	Brain Substantia Nigra	brain
33	chr18:43535400-43546400	Weak transcription	Rectal Mucosa Donor 31	rectum
34	chr18:43535600-43546400	Weak transcription	HUES64 Cell Line	embryonic stem cell
35	chr18:43535600-43546400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
36	chr18:43535600-43546400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
37	chr18:43535600-43546400	Weak transcription	Fetal Lung	lung
38	chr18:43535800-43545800	Weak transcription	Colonic Mucosa	Colon
39	chr18:43535800-43546600	Weak transcription	Sigmoid Colon	Sigmoid Colon
40	chr18:43536000-43545400	Weak transcription	Duodenum Smooth Muscle	Duodenum
41	chr18:43536000-43545800	Weak transcription	Rectal Mucosa Donor 29	rectum
42	chr18:43536200-43545200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr18:43536200-43545400	Weak transcription	Liver	Liver
44	chr18:43536200-43546200	Weak transcription	Fetal Brain Female	brain
45	chr18:43536200-43546400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr18:43536200-43546400	Weak transcription	HUES48 Cell Line	embryonic stem cell
47	chr18:43536400-43545800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr18:43537400-43546400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
49	chr18:43538000-43544600	Weak transcription	Ovary	ovary
50	chr18:43538400-43545400	Weak transcription	Fetal Kidney	kidney

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