Variant report

Variant	esv2757673
Chromosome Location	chr18:29632749-29674992
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1113)
CpG islands
(count:1101)
Chromatin interactive
region (count:44)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:1113 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:29672621-29672760	HepG2	liver:	n/a	n/a
2	ARID3A	chr18:29673359-29673884	K562	blood:	n/a	n/a
3	ARID3A	chr18:29671653-29671722	K562	blood:	n/a	n/a
4	ARID3A	chr18:29670540-29670822	HepG2	liver:	n/a	n/a
5	ARID3A	chr18:29671473-29672011	HepG2	liver:	n/a	n/a
6	ARID3A	chr18:29652345-29652621	HepG2	liver:	n/a	n/a
7	ARID3A	chr18:29652341-29652647	K562	blood:	n/a	n/a
8	ATF1	chr18:29671608-29672725	K562	blood:	n/a	n/a
9	ATF1	chr18:29640546-29640706	K562	blood:	n/a	n/a
10	ATF2	chr18:29671514-29672075	GM12878	blood:	n/a	n/a
11	ATF2	chr18:29665082-29665449	GM12878	blood:	n/a	n/a
12	ATF2	chr18:29672238-29673045	GM12878	blood:	n/a	n/a
13	ATF2	chr18:29665004-29665523	GM12878	blood:	n/a	n/a
14	ATF2	chr18:29671493-29672135	GM12878	blood:	n/a	n/a
15	ATF3	chr18:29671643-29671995	K562	blood:	n/a	chr18:29671812-29671823 chr18:29671810-29671825 chr18:29671814-29671822 chr18:29671772-29671781 chr18:29671812-29671823
16	BACH1	chr18:29672455-29672620	H1-hESC	embryonic stem cell:	n/a	n/a
17	BATF	chr18:29671727-29671953	GM12878	blood:	n/a	n/a
18	BATF	chr18:29672599-29672844	GM12878	blood:	n/a	n/a
19	BCL11A	chr18:29665138-29665493	GM12878	blood:	n/a	n/a
20	BCL11A	chr18:29665198-29665428	GM12878	blood:	n/a	n/a
21	BCLAF1	chr18:29671454-29672193	GM12878	blood:	n/a	chr18:29671982-29671995 chr18:29671983-29671992
22	BCLAF1	chr18:29665091-29665449	GM12878	blood:	n/a	n/a
23	BCLAF1	chr18:29664942-29665471	GM12878	blood:	n/a	n/a
24	BCLAF1	chr18:29671581-29672203	GM12878	blood:	n/a	chr18:29671982-29671995 chr18:29671983-29671992
25	BCLAF1	chr18:29672572-29673015	GM12878	blood:	n/a	chr18:29672947-29672960 chr18:29672946-29672955 chr18:29672940-29672953
26	BCLAF1	chr18:29673033-29673725	GM12878	blood:	n/a	n/a
27	BHLHE40	chr18:29671724-29673057	HepG2	liver:	n/a	chr18:29672946-29672962 chr18:29671977-29671993 chr18:29671974-29671990
28	BHLHE40	chr18:29671631-29673783	K562	blood:	n/a	chr18:29672946-29672962 chr18:29671977-29671993 chr18:29671974-29671990
29	BHLHE40	chr18:29672447-29672717	HepG2	liver:	n/a	n/a
30	BHLHE40	chr18:29672415-29672941	A549	lung:	n/a	n/a
31	BHLHE40	chr18:29671540-29673692	GM12878	blood:	n/a	chr18:29672946-29672962 chr18:29671977-29671993 chr18:29671974-29671990
32	BHLHE40	chr18:29665096-29665408	GM12878	blood:	n/a	n/a
33	BRCA1	chr18:29671668-29672012	H1-hESC	embryonic stem cell:	n/a	n/a
34	BRCA1	chr18:29672168-29672315	HepG2	liver:	n/a	n/a
35	BRCA1	chr18:29671503-29672004	Hela-S3	cervix:	n/a	n/a
36	BRCA1	chr18:29672674-29672854	HepG2	liver:	n/a	n/a
37	BRCA1	chr18:29671717-29671983	GM12878	blood:	n/a	n/a
38	BRCA1	chr18:29671833-29671910	HepG2	liver:	n/a	n/a
39	BRCA1	chr18:29672610-29672932	GM12878	blood:	n/a	n/a
40	BRCA1	chr18:29672395-29672879	Hela-S3	cervix:	n/a	n/a
41	CBX3	chr18:29671556-29672903	K562	blood:	n/a	n/a
42	CBX3	chr18:29664887-29665486	HCT-116	colon:	n/a	n/a
43	CBX3	chr18:29664909-29665472	HCT-116	colon:	n/a	n/a
44	CCNT2	chr18:29671651-29673750	K562	blood:	n/a	chr18:29672596-29672605 chr18:29672293-29672302 chr18:29673658-29673678 chr18:29672990-29672999 chr18:29672227-29672236 chr18:29672862-29672871 chr18:29672637-29672646
45	CCNT2	chr18:29637691-29637926	K562	blood:	n/a	n/a
46	CEBPB	chr18:29658270-29658302	K562	blood:	n/a	n/a
47	CEBPB	chr18:29672225-29673448	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr18:29664784-29665497	HCT-116	colon:	n/a	n/a
49	CEBPB	chr18:29671612-29672017	K562	blood:	n/a	n/a
50	CEBPB	chr18:29660479-29660748	A549	lung:	n/a	chr18:29660614-29660625

(count:1101 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:29673246-29673296	HPAEpiC	pulmonary alveolar:	n/a
2	chr18:29672549-29672599	NHBE	bronchial:	n/a
3	chr18:29673278-29673328	SAEC	small airway:	n/a
4	chr18:29673246-29673296	HPAEpiC	pulmonary alveolar:	n/a
5	chr18:29672549-29672599	NHBE	bronchial:	n/a
6	chr18:29673278-29673328	SAEC	small airway:	n/a
7	chr18:29669225-29669275	HMEC	breast:	n/a
8	chr18:29672450-29672500	Jurkat	blood:	n/a
9	chr18:29672468-29672518	HRCEpiC	kidney:	n/a
10	chr18:29672736-29672786	HMEC	breast:	n/a
11	chr18:29671767-29671817	PANC-1	pancreas:	n/a
12	chr18:29673278-29673328	GM06990	blood:	n/a
13	chr18:29671767-29671817	AG10803	skin:	n/a
14	chr18:29672549-29672599	NT2-D1	testis:	n/a
15	chr18:29673278-29673328	HCPEpiC	choroid plexus:	n/a
16	chr18:29671984-29672034	GM19239	blood:	n/a
17	chr18:29671767-29671817	HEEpiC	esophagus:	n/a
18	chr18:29671984-29672034	HL-60	blood:	n/a
19	chr18:29669225-29669275	HNPCEpiC	eye:	n/a
20	chr18:29673278-29673328	Caco-2	colon:	n/a
21	chr18:29673246-29673296	AG04450	lung:	fetal
22	chr18:29671448-29671498	HCT-116	colon:	n/a
23	chr18:29671984-29672034	SK-N-SH	brain:	n/a
24	chr18:29672468-29672518	AoSMC	blood vessel:	n/a
25	chr18:29671767-29671817	U87	brain:	n/a
26	chr18:29672450-29672500	T-47D	breast:	n/a
27	chr18:29672736-29672786	NT2-D1	testis:	n/a
28	chr18:29671618-29671668	HMEC	breast:	n/a
29	chr18:29669225-29669275	HAEpiC	amniotic membrane:	n/a
30	chr18:29672458-29672508	SK-N-MC	brain:	n/a
31	chr18:29673278-29673328	HRPEpiC	eye:	n/a
32	chr18:29672736-29672786	AG09319	gingival:	n/a
33	chr18:29672555-29672605	AG09319	gingival:	n/a
34	chr18:29673246-29673296	GM12878	blood:	n/a
35	chr18:29673246-29673296	Caco-2	colon:	n/a
36	chr18:29672450-29672500	HEEpiC	esophagus:	n/a
37	chr18:29672549-29672599	GM12891	blood:	n/a
38	chr18:29672468-29672518	HCT-116	colon:	n/a
39	chr18:29672555-29672605	HIPEpiC	eye:	n/a
40	chr18:29673278-29673328	HUVEC	blood vessel:	n/a
41	chr18:29672458-29672508	BE2_C	brain:	n/a
42	chr18:29672458-29672508	GM19239	blood:	n/a
43	chr18:29674872-29674922	U87	brain:	n/a
44	chr18:29671772-29671822	NHBE	bronchial:	n/a
45	chr18:29672555-29672605	SK-N-SH_RA	brain:	n/a
46	chr18:29672450-29672500	A549	lung:	n/a
47	chr18:29671618-29671668	T-47D	breast:	n/a
48	chr18:29671984-29672034	HRPEpiC	eye:	n/a
49	chr18:29672535-29672585	GM12891	blood:	n/a
50	chr18:29671448-29671498	HCF	heart:	n/a

(count:44 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:29651053..29654185-chr18:29670449..29673548,3	K562	blood:
2	chr18:29598540..29599388-chr18:29671670..29672456,2	Hela-S3	cervix:
3	chr18:29666841..29669333-chr18:29671631..29673559,3	MCF-7	breast:
4	chr18:29620883..29622757-chr18:29645869..29647631,2	K562	blood:
5	chr18:29521939..29525237-chr18:29670716..29673913,4	MCF-7	breast:
6	chr18:29627167..29630199-chr18:29636051..29638994,4	MCF-7	breast:
7	chr18:29661516..29666367-chr18:29670429..29672911,6	MCF-7	breast:
8	chr18:29671668..29674127-chr18:29674569..29677601,3	MCF-7	breast:
9	chr18:29596689..29599956-chr18:29670764..29674475,6	MCF-7	breast:
10	chr18:29628181..29630533-chr18:29631429..29634258,2	K562	blood:
11	chr12:120972120..120972749-chr18:29671926..29672687,2	Hela-S3	cervix:
12	chr18:29523882..29525586-chr18:29646566..29649385,2	K562	blood:
13	chr18:29641006..29643778-chr18:29670687..29672553,2	K562	blood:
14	chr11:62608032..62609663-chr18:29672517..29674072,2	MCF-7	breast:
15	chr18:29656745..29659248-chr18:29670363..29672023,2	K562	blood:
16	chr18:29521522..29523729-chr18:29672844..29674625,2	MCF-7	breast:
17	chr18:29672647..29674860-chr18:29703384..29706167,2	MCF-7	breast:
18	chr18:29654269..29657288-chr18:29670351..29673351,3	K562	blood:
19	chr18:29636110..29637655-chr18:29646609..29648361,2	K562	blood:
20	chr18:29652389..29654185-chr18:29671814..29673548,2	K562	blood:
21	chr18:29634515..29636379-chr18:29669677..29672287,2	K562	blood:
22	chr18:29654269..29657288-chr18:29670351..29673351,3	K562	blood:
23	chr17:73150233..73150854-chr18:29672091..29672842,2	HCT-116	colon:
24	chr18:29636110..29637655-chr18:29646609..29648361,2	K562	blood:
25	chr18:29657548..29661977-chr18:29669149..29673484,4	K562	blood:
26	chr18:29598038..29600342-chr18:29668214..29669893,2	MCF-7	breast:
27	chr18:29597506..29599866-chr18:29670953..29673378,4	MCF-7	breast:
28	chr18:29660336..29661951-chr18:29664954..29667841,2	K562	blood:
29	chr18:29660336..29661951-chr18:29664954..29667841,2	K562	blood:
30	chr18:29662644..29667608-chr18:29668028..29673014,9	K562	blood:
31	chr18:29645971..29648170-chr18:29655121..29657233,2	K562	blood:
32	chr18:29521618..29525019-chr18:29670361..29672184,4	MCF-7	breast:
33	chr18:29671880..29672426-chrX:131157129..131157907,2	Hela-S3	cervix:
34	chr18:29637884..29642506-chr18:29670649..29674281,4	K562	blood:
35	chr18:29653056..29654979-chr18:29671460..29672978,2	MCF-7	breast:
36	chr18:29520857..29524705-chr18:29670705..29674434,7	K562	blood:
37	chr18:29671417..29672347-chr20:42086520..42087354,2	Hela-S3	cervix:
38	chr17:42976409..42976919-chr18:29671871..29672426,2	Hela-S3	cervix:
39	chr11:65190111..65190616-chr18:29672226..29673180,2	Hela-S3	cervix:
40	chr18:29671926..29672642-chr3:159481391..159482087,2	Hela-S3	cervix:
41	chr18:29637884..29642506-chr18:29670649..29674281,4	K562	blood:
42	chr18:29670755..29674701-chr18:29702072..29706406,4	K562	blood:
43	chr18:29521537..29525393-chr18:29670839..29674328,7	K562	blood:
44	chr18:29671504..29673421-chr18:30049351..30052237,2	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RNF125-4	chr18:29671865-29672198	NONHSAT058853
2	lnc-TRAPPC8-1	chr18:29652700-29652841	ENSG00000263664.1
3	lnc-RNF125-4	chr18:29671847-29672198	NONHSAT058852
4	lnc-TRAPPC8-1	chr18:29652866-29652992	ENSG00000263664.1
5	lnc-TRAPPC8-2	chr18:29671818-29672082	ENSG00000265008.1
6	lnc-RNF125-4	chr18:29672663-29672849	NONHSAT058853
7	lnc-TRAPPC8-4	chr18:29655848-29656235	NONHSAT058850
8	lnc-RNF125-4	chr18:29672663-29672849	NONHSAT058852
9	lnc-TRAPPC8-2	chr18:29671258-29671465	ENSG00000265008.1

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	RNF125	hsa-miR-320a	chr18:29652419-29652425
2	RNF125	hsa-miR-320a	chr18:29649375-29649398
3	RNF125	hsa-miR-26b-5p	chr18:29651533-29651553

Variant related genes	Relation type
ENSG00000265008	TF binding region
ENSG00000238982	TF binding region
RNF138	TF binding region
ENSG00000265063	TF binding region
ENSG00000214917	TF binding region
ENSG00000265008	CpG island
ENSG00000238982	CpG island
RNF138	CpG island
ENSG00000265063	CpG island
ENSG00000214917	CpG island
ENSG00000265008	chromatin interactions
ENSG00000263393	chromatin interactions
ENSG00000134602	chromatin interactions
ENSG00000141441	chromatin interactions
ENSG00000167131	chromatin interactions
ENSG00000189159	chromatin interactions
ENSG00000108883	chromatin interactions
ENSG00000153339	chromatin interactions
ENSG00000022840	chromatin interactions
ENSG00000124193	chromatin interactions
ENSG00000263917	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000245532	chromatin interactions
ENSG00000250588	chromatin interactions
ENSG00000214917	chromatin interactions
ENSG00000134758	chromatin interactions
ENSG00000265063	chromatin interactions
ENSG00000101695	chromatin interactions
ENSG00000263823	chromatin interactions
ENSG00000110871	chromatin interactions

Extended variants
information (count: 1531 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:1531 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs61038301	chr18:29632749-29632750	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs539540456	chr18:29632759-29632760	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs539686227	chr18:29632764-29632765	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs558327050	chr18:29632834-29632835	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs57807662	chr18:29632906-29632907	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs544061950	chr18:29632912-29632913	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs576171284	chr18:29632931-29632932	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs184194421	chr18:29632945-29632946	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs73954986	chr18:29632947-29632948	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs541011915	chr18:29632975-29632976	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs150107853	chr18:29632991-29632992	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs189961380	chr18:29633045-29633046	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs59338045	chr18:29633051-29633052	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs375329067	chr18:29633083-29633084	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs563459511	chr18:29633113-29633114	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs141733314	chr18:29633115-29633116	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs56165282	chr18:29633131-29633132	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs181228449	chr18:29633137-29633138	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs567541781	chr18:29633154-29633155	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs146286419	chr18:29633181-29633182	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs546609380	chr18:29633209-29633210	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs546284192	chr18:29633240-29633241	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs538679649	chr18:29633249-29633250	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs371350625	chr18:29633265-29633266	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs59117416	chr18:29633330-29633331	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs61628852	chr18:29633371-29633372	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs570203610	chr18:29633390-29633391	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs57270876	chr18:29633394-29633395	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs376698351	chr18:29633395-29633396	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs397966355	chr18:29633396-29633397	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs12455805	chr18:29633434-29633435	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs59945357	chr18:29633441-29633442	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs12455807	chr18:29633448-29633449	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs56403688	chr18:29633473-29633474	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs115991052	chr18:29633527-29633528	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs578042349	chr18:29633547-29633548	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs200746781	chr18:29633585-29633586	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs60933882	chr18:29633592-29633593	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs61224386	chr18:29633602-29633603	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs545909968	chr18:29633655-29633656	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs570416422	chr18:29633686-29633687	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs542825132	chr18:29633724-29633725	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs572359734	chr18:29633732-29633733	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs561207649	chr18:29633744-29633745	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs528390997	chr18:29633832-29633833	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs149352934	chr18:29633864-29633865	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs187133155	chr18:29633867-29633868	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs79575770	chr18:29633868-29633869	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs190625317	chr18:29633869-29633870	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs11874448	chr18:29633881-29633882	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:70)

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
Prostate cancer	22341455	CNVD

Chromatin state (count:1162 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:29602600-29664200	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr18:29604600-29656000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr18:29606800-29637000	Weak transcription	Brain Anterior Caudate	brain
4	chr18:29615200-29648400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr18:29616000-29640200	Weak transcription	Esophagus	oesophagus
6	chr18:29618400-29639800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr18:29618400-29646800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr18:29618600-29642800	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr18:29619400-29645400	Weak transcription	Fetal Stomach	stomach
10	chr18:29622800-29639800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr18:29626000-29657200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr18:29626200-29639800	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr18:29627000-29637600	Weak transcription	HUES64 Cell Line	embryonic stem cell
14	chr18:29627400-29637600	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr18:29629000-29633400	Weak transcription	Fetal Muscle Trunk	muscle
16	chr18:29629200-29635000	Weak transcription	Lung	lung
17	chr18:29629200-29638200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
18	chr18:29630000-29633800	Weak transcription	Brain Cingulate Gyrus	brain
19	chr18:29630000-29637800	Weak transcription	Right Atrium	heart
20	chr18:29630000-29638800	Weak transcription	Liver	Liver
21	chr18:29630000-29640200	Weak transcription	Thymus	Thymus
22	chr18:29630000-29646600	Weak transcription	Sigmoid Colon	Sigmoid Colon
23	chr18:29630000-29664400	Weak transcription	Fetal Muscle Leg	muscle
24	chr18:29630200-29635200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
25	chr18:29630200-29635200	Weak transcription	Adipose Nuclei	Adipose
26	chr18:29630200-29636400	Weak transcription	Rectal Mucosa Donor 31	rectum
27	chr18:29630200-29646400	Weak transcription	Primary B cells from peripheral blood	blood
28	chr18:29630400-29636200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
29	chr18:29630400-29646600	Weak transcription	Duodenum Mucosa	Duodenum
30	chr18:29630400-29650800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr18:29630400-29664400	Weak transcription	Left Ventricle	heart
32	chr18:29630600-29635000	Weak transcription	Fetal Thymus	thymus
33	chr18:29630800-29633400	Weak transcription	Fetal Intestine Small	intestine
34	chr18:29630800-29634800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
35	chr18:29630800-29637800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
36	chr18:29630800-29641800	Weak transcription	Primary B cells from cord blood	blood
37	chr18:29630800-29658600	Weak transcription	Rectal Mucosa Donor 29	rectum
38	chr18:29631000-29636200	Weak transcription	Fetal Intestine Large	intestine
39	chr18:29631200-29633800	Weak transcription	Monocytes-CD14+_RO01746	blood
40	chr18:29631200-29634200	Strong transcription	Primary T cells from cord blood	blood
41	chr18:29631200-29634400	Weak transcription	Primary T helper cells PMA-I stimulated	--
42	chr18:29631200-29640800	Weak transcription	Primary hematopoietic stem cells	blood
43	chr18:29631400-29634400	Weak transcription	Primary monocytes fromperipheralblood	blood
44	chr18:29631400-29636200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
45	chr18:29631400-29636600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr18:29631400-29639000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
47	chr18:29631400-29671400	Weak transcription	Hela-S3	cervix
48	chr18:29631600-29632800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
49	chr18:29631600-29637800	Strong transcription	Primary T cells fromperipheralblood	blood
50	chr18:29631800-29635800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood

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