Variant report

Variant	nsv1008886
Chromosome Location	chr1:242015591-242176983
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1790)
CpG islands
(count:1221)
Chromatin interactive
region (count:100)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1790 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:242139649-242139760	K562	blood:	n/a	n/a
2	ARID3A	chr1:242059677-242060049	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:242149085-242149421	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:242107314-242107371	K562	blood:	n/a	n/a
5	ARID3A	chr1:242079607-242079807	HepG2	liver:	n/a	n/a
6	ARID3A	chr1:242149175-242149484	K562	blood:	n/a	n/a
7	ARID3A	chr1:242059728-242060038	K562	blood:	n/a	n/a
8	ARID3A	chr1:242097404-242097718	HepG2	liver:	n/a	n/a
9	ARID3A	chr1:242135954-242136215	HepG2	liver:	n/a	n/a
10	ARID3A	chr1:242087569-242087783	HepG2	liver:	n/a	n/a
11	ATF1	chr1:242139514-242139860	K562	blood:	n/a	n/a
12	ATF1	chr1:242130694-242130726	K562	blood:	n/a	n/a
13	ATF1	chr1:242172320-242172434	K562	blood:	n/a	n/a
14	ATF1	chr1:242058327-242058480	K562	blood:	n/a	n/a
15	ATF1	chr1:242059628-242059975	K562	blood:	n/a	n/a
16	ATF1	chr1:242147616-242147938	K562	blood:	n/a	n/a
17	ATF1	chr1:242128209-242128497	K562	blood:	n/a	n/a
18	ATF1	chr1:242137853-242137919	K562	blood:	n/a	n/a
19	ATF2	chr1:242161604-242162019	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF2	chr1:242097401-242097898	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF2	chr1:242097445-242097923	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF2	chr1:242161623-242162128	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF3	chr1:242136065-242136245	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF3	chr1:242136045-242136302	K562	blood:	n/a	n/a
25	ATF3	chr1:242153332-242153616	K562	blood:	n/a	n/a
26	BACH1	chr1:242044778-242045267	K562	blood:	n/a	n/a
27	BACH1	chr1:242161817-242162371	H1-hESC	embryonic stem cell:	n/a	n/a
28	BATF	chr1:242152456-242152709	GM12878	blood:	n/a	n/a
29	BATF	chr1:242058396-242058614	GM12878	blood:	n/a	chr1:242058494-242058505
30	BATF	chr1:242058355-242058646	GM12878	blood:	n/a	chr1:242058494-242058505
31	BCL11A	chr1:242152382-242152691	GM12878	blood:	n/a	n/a
32	BCL3	chr1:242161671-242162382	A549	lung:	n/a	n/a
33	BCL3	chr1:242161617-242162295	A549	lung:	n/a	n/a
34	BHLHE40	chr1:242121224-242121872	K562	blood:	n/a	n/a
35	BHLHE40	chr1:242106090-242106337	K562	blood:	n/a	chr1:242106181-242106190 chr1:242106180-242106189 chr1:242106180-242106189
36	BHLHE40	chr1:242161685-242162227	K562	blood:	n/a	chr1:242162042-242162058
37	BHLHE40	chr1:242069373-242069700	K562	blood:	n/a	n/a
38	BHLHE40	chr1:242153309-242153692	K562	blood:	n/a	chr1:242153473-242153482 chr1:242153473-242153482 chr1:242153467-242153488 chr1:242153472-242153481
39	BHLHE40	chr1:242152479-242152805	GM12878	blood:	n/a	n/a
40	BHLHE40	chr1:242020408-242020638	GM12878	blood:	n/a	n/a
41	BHLHE40	chr1:242111843-242111974	K562	blood:	n/a	n/a
42	BRCA1	chr1:242169360-242169754	Hela-S3	cervix:	n/a	n/a
43	BRCA1	chr1:242161887-242162178	Hela-S3	cervix:	n/a	n/a
44	CBX3	chr1:242161511-242162367	HCT-116	colon:	n/a	n/a
45	CBX3	chr1:242121536-242121885	K562	blood:	n/a	n/a
46	CBX3	chr1:242161587-242162212	K562	blood:	n/a	n/a
47	CBX3	chr1:242147583-242147949	K562	blood:	n/a	n/a
48	CBX3	chr1:242161494-242162370	HCT-116	colon:	n/a	n/a
49	CBX3	chr1:242161655-242162161	K562	blood:	n/a	n/a
50	CCNT2	chr1:242161625-242162175	K562	blood:	n/a	chr1:242162035-242162044

(count:1221 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:242162828-242162878	NHDF-neo	bronchial:	n/a
2	chr1:242162828-242162878	NHDF-neo	bronchial:	n/a
3	chr1:242121827-242121877	Hepatocyte	liver:	n/a
4	chr1:242142508-242142558	GM12891	blood:	n/a
5	chr1:242030232-242030282	NT2-D1	testis:	n/a
6	chr1:242052841-242052891	SK-N-SH	brain:	n/a
7	chr1:242142508-242142558	BE2_C	brain:	n/a
8	chr1:242097870-242097920	Caco-2	colon:	n/a
9	chr1:242163517-242163567	HEK293	kidney:	embryo
10	chr1:242044107-242044157	NHBE	bronchial:	n/a
11	chr1:242122063-242122113	ovcar-3	ovarian:	n/a
12	chr1:242121827-242121877	ProgFib	skin:	n/a
13	chr1:242120638-242120688	SK-N-SH_RA	brain:	n/a
14	chr1:242122063-242122113	IMR90	lung:	fetal
15	chr1:242030232-242030282	SK-N-SH_RA	brain:	n/a
16	chr1:242162802-242162852	HMEC	breast:	n/a
17	chr1:242052841-242052891	MCF10A-Er-Src	breast:	n/a
18	chr1:242122063-242122113	MCF-7	breast:	n/a
19	chr1:242120638-242120688	BE2_C	brain:	n/a
20	chr1:242120638-242120688	A549	lung:	n/a
21	chr1:242162828-242162878	GM19239	blood:	n/a
22	chr1:242142475-242142525	IMR90	lung:	fetal
23	chr1:242142475-242142525	PrEC	prostate:	n/a
24	chr1:242161780-242161830	LNCaP	prostate:	n/a
25	chr1:242052841-242052891	HNPCEpiC	eye:	n/a
26	chr1:242161881-242161931	U87	brain:	n/a
27	chr1:242161806-242161856	AoSMC	blood vessel:	n/a
28	chr1:242097870-242097920	ECC-1	luminal epithelium:	n/a
29	chr1:242161780-242161830	GM12891	blood:	n/a
30	chr1:242161806-242161856	GM12878	blood:	n/a
31	chr1:242162802-242162852	A549	lung:	n/a
32	chr1:242044107-242044157	HAEpiC	amniotic membrane:	n/a
33	chr1:242161780-242161830	AG09309	skin:	n/a
34	chr1:242142508-242142558	BJ	skin:	n/a
35	chr1:242097870-242097920	HEEpiC	esophagus:	n/a
36	chr1:242162828-242162878	CMK	blood:	n/a
37	chr1:242052841-242052891	MCF-7	breast:	n/a
38	chr1:242121526-242121576	GM06990	blood:	n/a
39	chr1:242161881-242161931	SK-N-MC	brain:	n/a
40	chr1:242052841-242052891	HEK293	kidney:	embryo
41	chr1:242121230-242121280	IMR90	lung:	fetal
42	chr1:242121526-242121576	AoSMC	blood vessel:	n/a
43	chr1:242121526-242121576	AG04450	lung:	fetal
44	chr1:242097870-242097920	SK-N-SH	brain:	n/a
45	chr1:242121827-242121877	NHDF-neo	bronchial:	n/a
46	chr1:242161780-242161830	MCF-7	breast:	n/a
47	chr1:242121827-242121877	PrEC	prostate:	n/a
48	chr1:242121526-242121576	HCM	heart:	n/a
49	chr1:242162802-242162852	HL-60	blood:	n/a
50	chr1:242161806-242161856	HRCEpiC	kidney:	n/a

(count:100 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:242034731..242037217-chr1:242045770..242047901,2	K562	blood:
2	chr1:242059371..242060335-chr1:242161395..242162231,4	MCF-7	breast:
3	chr1:242011267..242015099-chr1:242035784..242038875,4	K562	blood:
4	chr1:241767091..241768658-chr1:242019786..242021766,2	K562	blood:
5	chr1:242059673..242060311-chr1:242149546..242150431,2	MCF-7	breast:
6	chr1:241774093..241774637-chr1:242059374..242059913,2	K562	blood:
7	chr1:242026543..242030439-chr1:242041190..242044966,5	K562	blood:
8	chr1:241694305..241695206-chr1:242161362..242162044,2	K562	blood:
9	chr1:241774407..241775239-chr1:242148964..242149557,2	MCF-7	breast:
10	chr1:242059414..242060329-chr1:242180301..242181638,4	K562	blood:
11	chr1:241774424..241775122-chr1:242161574..242162262,2	MCF-7	breast:
12	chr1:242030614..242036400-chr1:242037381..242042163,8	K562	blood:
13	chr1:242082815..242084795-chr1:242086040..242088718,2	K562	blood:
14	chr1:242102983..242105016-chr1:242106501..242108855,2	MCF-7	breast:
15	chr1:242082251..242084626-chr1:242095410..242097827,2	K562	blood:
16	chr1:242082251..242084626-chr1:242095410..242097827,2	K562	blood:
17	chr1:242010596..242013102-chr1:242058609..242060123,2	K562	blood:
18	chr1:242144580..242146530-chr1:242152140..242153827,2	K562	blood:
19	chr1:242022992..242027176-chr1:242044979..242047845,3	K562	blood:
20	chr1:242101934..242104578-chr1:242110497..242113039,2	K562	blood:
21	chr1:242130029..242131689-chr1:242138065..242140950,2	K562	blood:
22	chr1:242103745..242105916-chr1:242116702..242119562,2	K562	blood:
23	chr1:242060961..242063036-chr1:242175225..242177165,2	K562	blood:
24	chr1:242059480..242060334-chr1:242148747..242149804,4	K562	blood:
25	chr1:242059953..242061763-chr1:242068532..242070106,2	K562	blood:
26	chr1:242059953..242061763-chr1:242068532..242070106,2	K562	blood:
27	chr1:242059370..242060370-chr1:242148860..242150209,7	MCF-7	breast:
28	chr1:242096785..242098721-chr1:242103500..242105954,2	K562	blood:
29	chr1:241852237..241854892-chr1:242017899..242019759,2	K562	blood:
30	chr1:241681618..241683927-chr1:242037772..242040748,2	K562	blood:
31	chr1:242059371..242060335-chr1:242161395..242162231,4	MCF-7	breast:
32	chr1:242130029..242131689-chr1:242138065..242140950,2	K562	blood:
33	chr1:242059370..242060370-chr1:242148860..242150209,7	MCF-7	breast:
34	chr1:242161372..242162202-chr1:242171638..242172445,2	K562	blood:
35	chr1:242082815..242084795-chr1:242086040..242088718,2	K562	blood:
36	chr1:242034800..242036646-chr1:242037118..242039497,2	MCF-7	breast:
37	chr1:242080921..242083075-chr1:242088062..242090649,2	MCF-7	breast:
38	chr1:242022063..242023665-chr1:242035192..242037679,2	K562	blood:
39	chr1:242063118..242065688-chr1:242068745..242071369,2	K562	blood:
40	chr1:242026426..242029268-chr1:242029901..242034404,4	K562	blood:
41	chr1:241913661..241915313-chr1:242019528..242022307,2	K562	blood:
42	chr1:242144580..242146530-chr1:242152140..242153827,2	K562	blood:
43	chr1:242059788..242060336-chr1:242180683..242181366,2	MCF-7	breast:
44	chr1:242030614..242036400-chr1:242037381..242042163,8	K562	blood:
45	chr1:242014950..242016521-chr1:242022226..242025203,2	MCF-7	breast:
46	chr1:242066650..242069303-chr1:242074434..242076420,2	K562	blood:
47	chr1:242037775..242040488-chr1:242043413..242045224,4	K562	blood:
48	chr1:242059673..242060311-chr1:242149546..242150431,2	MCF-7	breast:
49	chr1:242063761..242065381-chr1:242152078..242153652,2	MCF-7	breast:
50	chr1:242014950..242016521-chr1:242022226..242025203,2	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EXO1-1	chr1:242071423-242071511	NONHSAT010556
2	lnc-EXO1-8	chr1:242147327-242147451	ucscGeneNc_uc001iac_2
3	lnc-EXO1-8	chr1:242147327-242147451	NONHSAT010559
4	lnc-EXO1-1	chr1:242061356-242061975	NONHSAT010556
5	lnc-EXO1-1	chr1:242072153-242072836	NONHSAT010556
6	lnc-EXO1-1	chr1:242072240-242072365	XLOC_000638
7	lnc-EXO1-1	chr1:242074676-242075035	XLOC_000638
8	lnc-EXO1-5	chr1:242079425-242079845	NONHSAT010558

No data

Variant related genes	Relation type
EXO1	TF binding region
BECN1P1	TF binding region
MAP1LC3C	TF binding region
CFL1P4	TF binding region
ENSG00000235990	TF binding region
EXO1	CpG island
BECN1P1	CpG island
MAP1LC3C	CpG island
CFL1P4	CpG island
ENSG00000235990	CpG island
ENSG00000091483	chromatin interactions
ENSG00000223119	chromatin interactions
ENSG00000054277	chromatin interactions
ENSG00000197769	chromatin interactions
ENSG00000174371	chromatin interactions
ENSG00000196289	chromatin interactions
ENSG00000117009	chromatin interactions
CCNE1	miRNA target sites

Extended variants
information (count: 7450 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:7450 , 50 per page) page: 1 2 3 4 5 6 7 ... 149

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4149863	chr1:242015591-242015592	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs200962199	chr1:242015608-242015609	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs370831732	chr1:242015622-242015623	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs113869435	chr1:242015625-242015626	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs199625132	chr1:242015649-242015650	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs141548668	chr1:242015657-242015658	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs4149864	chr1:242015658-242015659	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs150678179	chr1:242015676-242015677	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs147963292	chr1:242015699-242015700	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs187875457	chr1:242015704-242015705	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs4149865	chr1:242015709-242015710	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs192680726	chr1:242015712-242015713	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs200129097	chr1:242015735-242015736	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs534128907	chr1:242015743-242015744	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs185072087	chr1:242015744-242015745	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs528301976	chr1:242015747-242015748	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs376625539	chr1:242015765-242015766	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs571758243	chr1:242015774-242015775	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs2526704	chr1:242015820-242015821	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs557335631	chr1:242015823-242015824	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs114303747	chr1:242015886-242015887	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs536970892	chr1:242015905-242015906	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs553571134	chr1:242015923-242015924	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs573460460	chr1:242015950-242015951	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs4149866	chr1:242015952-242015953	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs539265011	chr1:242016019-242016020	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs377273638	chr1:242016051-242016052	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs577676150	chr1:242016084-242016085	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs543004167	chr1:242016139-242016140	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs77518709	chr1:242016195-242016196	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs376665576	chr1:242016219-242016220	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs555938287	chr1:242016239-242016240	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs563316807	chr1:242016343-242016344	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs368741734	chr1:242016381-242016382	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs139745272	chr1:242016437-242016438	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs397862999	chr1:242016438-242016439	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs573565126	chr1:242016443-242016444	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs542497879	chr1:242016444-242016445	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs143340737	chr1:242016451-242016452	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs528266928	chr1:242016492-242016493	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs79792692	chr1:242016511-242016512	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs551592115	chr1:242016526-242016527	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs4149867	chr1:242016590-242016591	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs562099707	chr1:242016599-242016600	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs368794651	chr1:242016600-242016601	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs542092590	chr1:242016630-242016631	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs148384257	chr1:242016633-242016634	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs550672150	chr1:242016646-242016647	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs369994389	chr1:242016653-242016654	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs567681802	chr1:242016700-242016701	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:98)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	21829676	CNVD
Hepatocellular carcinoma	16750200	CNVD
Arrhythmogenic right ventricular cardiomyopathy	17576883	CNVD
Multiple myeloma	16616336	CNVD
Developmental delay	21147756	CNVD
Ovarian cancer	21720365	CNVD
Glioblastoma multiforme	22291905	CNVD
Myelofibrosis	22110671	CNVD
Disease	21936942	CNVD
laryngomalacia	21936942	CNVD
GLUT3 deficiency syndrome	20509907	CNVD
Developmental delay	21373258	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Developmental delay	19490664	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Glioblastoma	18772890	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Brain overgrowth syndrome	24179207	CNVD
Breast cancer	22522925	CNVD
Acute lymphoblastic leukemia	21339820	CNVD

Chromatin state (count:1228 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:242012000-242021400	Weak transcription	Right Atrium	heart
2	chr1:242012000-242023800	Weak transcription	Stomach Mucosa	stomach
3	chr1:242012000-242032600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr1:242012200-242016800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr1:242012200-242025600	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr1:242012200-242027800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr1:242012200-242028600	Weak transcription	Gastric	stomach
8	chr1:242012200-242044000	Weak transcription	Primary B cells from cord blood	blood
9	chr1:242012400-242019400	Weak transcription	Fetal Brain Male	brain
10	chr1:242012400-242060200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr1:242012600-242016600	Weak transcription	Primary neutrophils fromperipheralblood	blood
12	chr1:242012600-242016800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr1:242012600-242023200	Weak transcription	Fetal Muscle Trunk	muscle
14	chr1:242012600-242051600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr1:242012600-242051800	Weak transcription	Duodenum Mucosa	Duodenum
16	chr1:242012800-242015800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr1:242012800-242016400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr1:242012800-242016800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr1:242012800-242017000	Weak transcription	Fetal Stomach	stomach
20	chr1:242012800-242019800	Weak transcription	Fetal Kidney	kidney
21	chr1:242012800-242020600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr1:242012800-242054600	Weak transcription	HSMM	muscle
23	chr1:242012800-242056000	Weak transcription	Fetal Intestine Small	intestine
24	chr1:242013000-242016800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
25	chr1:242013000-242017000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr1:242013000-242053400	Weak transcription	Fetal Lung	lung
27	chr1:242013200-242016400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr1:242013200-242016600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr1:242013200-242016600	Weak transcription	Fetal Brain Female	brain
30	chr1:242013200-242016800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr1:242013200-242016800	Weak transcription	Thymus	Thymus
32	chr1:242013200-242017000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr1:242013200-242017000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
34	chr1:242013200-242017800	Weak transcription	Esophagus	oesophagus
35	chr1:242013200-242018200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
36	chr1:242013200-242018400	Strong transcription	H9 Cell Line	embryonic stem cell
37	chr1:242013200-242018600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
38	chr1:242013200-242020400	Weak transcription	HUVEC	blood vessel
39	chr1:242013200-242022000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
40	chr1:242013200-242023800	Weak transcription	NH-A	brain
41	chr1:242013200-242028800	Strong transcription	H1 Cell Line	embryonic stem cell
42	chr1:242013200-242030000	Weak transcription	NHDF-Ad	bronchial
43	chr1:242013200-242030200	Weak transcription	Fetal Muscle Leg	muscle
44	chr1:242013200-242032400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr1:242013200-242034200	Weak transcription	Brain Germinal Matrix	brain
46	chr1:242013200-242036600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr1:242013200-242038800	Strong transcription	HUES6 Cell Line	embryonic stem cell
48	chr1:242013200-242042000	Weak transcription	HepG2	liver
49	chr1:242013200-242048000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr1:242013200-242053200	Weak transcription	Osteobl	bone

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