Variant report

Variant	nsv523554
Chromosome Location	chr1:242029101-242096551
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:489)
CpG islands
(count:183)
Chromatin interactive
region (count:51)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:242059677-242060049	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:242079607-242079807	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:242059728-242060038	K562	blood:	n/a	n/a
4	ARID3A	chr1:242087569-242087783	HepG2	liver:	n/a	n/a
5	ATF1	chr1:242058327-242058480	K562	blood:	n/a	n/a
6	ATF1	chr1:242059628-242059975	K562	blood:	n/a	n/a
7	BACH1	chr1:242044778-242045267	K562	blood:	n/a	n/a
8	BATF	chr1:242058355-242058646	GM12878	blood:	n/a	chr1:242058494-242058505
9	BATF	chr1:242058396-242058614	GM12878	blood:	n/a	chr1:242058494-242058505
10	BHLHE40	chr1:242069373-242069700	K562	blood:	n/a	n/a
11	CCNT2	chr1:242034620-242034900	K562	blood:	n/a	n/a
12	CEBPB	chr1:242092083-242092242	K562	blood:	n/a	n/a
13	CEBPB	chr1:242082242-242082595	IMR90	lung:	n/a	n/a
14	CEBPB	chr1:242081587-242081801	HepG2	liver:	n/a	n/a
15	CEBPB	chr1:242070320-242070589	K562	blood:	n/a	chr1:242070416-242070427
16	CEBPB	chr1:242070288-242070541	Hela-S3	cervix:	n/a	chr1:242070416-242070427
17	CEBPB	chr1:242058517-242058815	IMR90	lung:	n/a	chr1:242058668-242058679
18	CEBPB	chr1:242051454-242051942	IMR90	lung:	n/a	n/a
19	CEBPB	chr1:242058444-242058804	Hela-S3	cervix:	n/a	chr1:242058668-242058679
20	CEBPB	chr1:242070238-242070608	K562	blood:	n/a	chr1:242070416-242070427
21	CEBPB	chr1:242082322-242082445	HepG2	liver:	n/a	n/a
22	CEBPB	chr1:242070332-242070634	MCF-7	breast:	n/a	chr1:242070416-242070427
23	CEBPB	chr1:242070257-242070583	A549	lung:	n/a	chr1:242070416-242070427
24	CEBPB	chr1:242058510-242058811	HepG2	liver:	n/a	chr1:242058668-242058679
25	CEBPB	chr1:242058486-242058820	A549	lung:	n/a	chr1:242058668-242058679
26	CEBPB	chr1:242070269-242070594	H1-hESC	embryonic stem cell:	n/a	chr1:242070416-242070427
27	CEBPB	chr1:242070257-242070591	IMR90	lung:	n/a	chr1:242070416-242070427
28	CEBPB	chr1:242058496-242058753	A549	lung:	n/a	chr1:242058668-242058679
29	CEBPB	chr1:242082311-242082538	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr1:242081556-242081681	K562	blood:	n/a	n/a
31	CEBPB	chr1:242087523-242087823	HepG2	liver:	n/a	n/a
32	CEBPB	chr1:242070270-242070609	HepG2	liver:	n/a	chr1:242070416-242070427
33	CEBPB	chr1:242032324-242032646	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr1:242058518-242058784	K562	blood:	n/a	chr1:242058668-242058679
35	CTCF	chr1:242059820-242059970	GM12870	blood:	n/a	chr1:242059843-242059864 chr1:242059844-242059857 chr1:242059841-242059859
36	CTCF	chr1:242059737-242060002	SK-N-SH_RA	brain:	n/a	chr1:242059843-242059864 chr1:242059844-242059857 chr1:242059841-242059859
37	CTCF	chr1:242059706-242059988	A549	lung:	n/a	chr1:242059843-242059864 chr1:242059844-242059857 chr1:242059841-242059859
38	CTCF	chr1:242059800-242059950	GM12875	blood:	n/a	chr1:242059843-242059864 chr1:242059844-242059857 chr1:242059841-242059859
39	CTCF	chr1:242059760-242059910	GM12868	blood:	n/a	chr1:242059843-242059864 chr1:242059844-242059857 chr1:242059841-242059859
40	CTCF	chr1:242072080-242072230	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr1:242059780-242059930	HEEpiC	esophagus:	n/a	chr1:242059843-242059864 chr1:242059844-242059857 chr1:242059841-242059859
42	CTCF	chr1:242059517-242059569	GM19238	blood:	n/a	n/a
43	CTCF	chr1:242059760-242059910	HA-sp	spinal cord:	n/a	chr1:242059843-242059864 chr1:242059844-242059857 chr1:242059841-242059859
44	CTCF	chr1:242059738-242059966	Hela-S3	cervix:	n/a	chr1:242059843-242059864 chr1:242059844-242059857 chr1:242059841-242059859
45	CTCF	chr1:242059780-242059930	HCT-116	colon:	n/a	chr1:242059843-242059864 chr1:242059844-242059857 chr1:242059841-242059859
46	CTCF	chr1:242059760-242059910	SK-N-SH_RA	brain:	n/a	chr1:242059843-242059864 chr1:242059844-242059857 chr1:242059841-242059859
47	CTCF	chr1:242059800-242059950	HCPEpiC	choroid plexus:	n/a	chr1:242059843-242059864 chr1:242059844-242059857 chr1:242059841-242059859
48	CTCF	chr1:242059590-242060115	A549	lung:	n/a	chr1:242059843-242059864 chr1:242059844-242059857 chr1:242059841-242059859
49	CTCF	chr1:242059820-242059970	HVMF	connective:	n/a	chr1:242059843-242059864 chr1:242059844-242059857 chr1:242059841-242059859
50	CTCF	chr1:242059800-242059950	GM12878	blood:	n/a	chr1:242059843-242059864 chr1:242059844-242059857 chr1:242059841-242059859

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:242044107-242044157	ECC-1	luminal epithelium:	n/a
2	chr1:242052841-242052891	NB4	blood:	n/a
3	chr1:242030232-242030282	HCPEpiC	choroid plexus:	n/a
4	chr1:242044107-242044157	SK-N-MC	brain:	n/a
5	chr1:242030232-242030282	AG04450	lung:	fetal
6	chr1:242052841-242052891	AG09309	skin:	n/a
7	chr1:242030232-242030282	HIPEpiC	eye:	n/a
8	chr1:242052841-242052891	RPTEC	kidney:	n/a
9	chr1:242030232-242030282	SKMC	muscle:	n/a
10	chr1:242044107-242044157	HPAEpiC	pulmonary alveolar:	n/a
11	chr1:242052841-242052891	Hepatocyte	liver:	n/a
12	chr1:242052841-242052891	HRPEpiC	eye:	n/a
13	chr1:242052841-242052891	MCF10A-Er-Src	breast:	n/a
14	chr1:242030232-242030282	HepG2	liver:	n/a
15	chr1:242052841-242052891	PFSK-1	brain:	n/a
16	chr1:242052841-242052891	NHBE	bronchial:	n/a
17	chr1:242052841-242052891	HUVEC	blood vessel:	n/a
18	chr1:242030232-242030282	GM19239	blood:	n/a
19	chr1:242030232-242030282	NHBE	bronchial:	n/a
20	chr1:242052841-242052891	BE2_C	brain:	n/a
21	chr1:242052841-242052891	U87	brain:	n/a
22	chr1:242030232-242030282	SAEC	small airway:	n/a
23	chr1:242044107-242044157	U87	brain:	n/a
24	chr1:242030232-242030282	PrEC	prostate:	n/a
25	chr1:242044107-242044157	PANC-1	pancreas:	n/a
26	chr1:242030232-242030282	GM06990	blood:	n/a
27	chr1:242052841-242052891	HAEpiC	amniotic membrane:	n/a
28	chr1:242030232-242030282	CMK	blood:	n/a
29	chr1:242052841-242052891	SKMC	muscle:	n/a
30	chr1:242030232-242030282	Caco-2	colon:	n/a
31	chr1:242030232-242030282	T-47D	breast:	n/a
32	chr1:242052841-242052891	MCF-7	breast:	n/a
33	chr1:242044107-242044157	HCPEpiC	choroid plexus:	n/a
34	chr1:242052841-242052891	ProgFib	skin:	n/a
35	chr1:242044107-242044157	HAEpiC	amniotic membrane:	n/a
36	chr1:242044107-242044157	MCF-7	breast:	n/a
37	chr1:242052841-242052891	Hela-S3	cervix:	n/a
38	chr1:242030232-242030282	GM12891	blood:	n/a
39	chr1:242044107-242044157	NB4	blood:	n/a
40	chr1:242052841-242052891	NHDF-neo	bronchial:	n/a
41	chr1:242030232-242030282	HEEpiC	esophagus:	n/a
42	chr1:242052841-242052891	SK-N-MC	brain:	n/a
43	chr1:242044107-242044157	GM12891	blood:	n/a
44	chr1:242044107-242044157	Hela-S3	cervix:	n/a
45	chr1:242044107-242044157	RPTEC	kidney:	n/a
46	chr1:242052841-242052891	AG04449	skin:	fetal
47	chr1:242044107-242044157	HEK293	kidney:	embryo
48	chr1:242052841-242052891	GM06990	blood:	n/a
49	chr1:242030232-242030282	HPAEpiC	pulmonary alveolar:	n/a
50	chr1:242030232-242030282	AoSMC	blood vessel:	n/a

(count:51 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:242059953..242061763-chr1:242068532..242070106,2	K562	blood:
2	chr1:242034639..242037217-chr1:242050358..242052283,2	K562	blood:
3	chr1:242060961..242063036-chr1:242175225..242177165,2	K562	blood:
4	chr1:242034800..242036646-chr1:242037118..242039497,2	MCF-7	breast:
5	chr1:242082815..242084795-chr1:242086040..242088718,2	K562	blood:
6	chr1:242034639..242037217-chr1:242050358..242052283,2	K562	blood:
7	chr1:241788676..241790229-chr1:242053556..242055267,2	K562	blood:
8	chr1:242034800..242036646-chr1:242037118..242039497,2	MCF-7	breast:
9	chr1:242066650..242069303-chr1:242074434..242076420,2	K562	blood:
10	chr1:242041021..242042827-chr1:242044286..242047076,2	K562	blood:
11	chr1:242059414..242060329-chr1:242180301..242181638,4	K562	blood:
12	chr1:242059480..242060334-chr1:242148747..242149804,4	K562	blood:
13	chr1:242030614..242036400-chr1:242037381..242042163,8	K562	blood:
14	chr1:242019796..242021724-chr1:242031300..242034090,2	K562	blood:
15	chr1:242026426..242029268-chr1:242029901..242034404,4	K562	blood:
16	chr1:242037775..242040488-chr1:242043413..242045224,4	K562	blood:
17	chr1:242012519..242016019-chr1:242054606..242057342,3	K562	blood:
18	chr1:242010596..242013102-chr1:242058609..242060123,2	K562	blood:
19	chr1:242066650..242069303-chr1:242074434..242076420,2	K562	blood:
20	chr1:242030614..242036400-chr1:242037381..242042163,8	K562	blood:
21	chr1:242022992..242027176-chr1:242044979..242047845,3	K562	blood:
22	chr1:241774093..241774637-chr1:242059374..242059913,2	K562	blood:
23	chr1:241660789..241662817-chr1:242073077..242076000,2	K562	blood:
24	chr1:241681862..241683903-chr1:242032872..242034945,2	K562	blood:
25	chr1:242059953..242061763-chr1:242068532..242070106,2	K562	blood:
26	chr1:242063118..242065688-chr1:242068745..242071369,2	K562	blood:
27	chr1:242080921..242083075-chr1:242088062..242090649,2	MCF-7	breast:
28	chr1:242059673..242060311-chr1:242149546..242150431,2	MCF-7	breast:
29	chr1:242059370..242060370-chr1:242148860..242150209,7	MCF-7	breast:
30	chr1:242063761..242065381-chr1:242152078..242153652,2	MCF-7	breast:
31	chr1:242080921..242083075-chr1:242088062..242090649,2	MCF-7	breast:
32	chr1:242026543..242030439-chr1:242041190..242044966,5	K562	blood:
33	chr1:242079518..242081849-chr1:242083319..242086180,3	K562	blood:
34	chr1:242022063..242023665-chr1:242035192..242037679,2	K562	blood:
35	chr1:242079518..242081849-chr1:242083319..242086180,3	K562	blood:
36	chr1:242059371..242060335-chr1:242161395..242162231,4	MCF-7	breast:
37	chr1:242059788..242060336-chr1:242180683..242181366,2	MCF-7	breast:
38	chr1:242026426..242029268-chr1:242029901..242034404,4	K562	blood:
39	chr1:242034731..242037217-chr1:242045770..242047901,2	K562	blood:
40	chr1:242063118..242065688-chr1:242068745..242071369,2	K562	blood:
41	chr1:242011267..242015099-chr1:242035784..242038875,4	K562	blood:
42	chr1:242037775..242040488-chr1:242043413..242045224,4	K562	blood:
43	chr1:242059613..242060290-chr1:242179713..242180384,2	MCF-7	breast:
44	chr1:242012601..242013405-chr1:242037363..242038255,2	MCF-7	breast:
45	chr1:241681618..241683927-chr1:242037772..242040748,2	K562	blood:
46	chr1:242009621..242013856-chr1:242035396..242038763,5	MCF-7	breast:
47	chr1:242082251..242084626-chr1:242095410..242097827,2	K562	blood:
48	chr1:242059401..242060332-chr1:242161246..242162002,4	K562	blood:
49	chr1:242034731..242037217-chr1:242045770..242047901,2	K562	blood:
50	chr1:242082815..242084795-chr1:242086040..242088718,2	K562	blood:

(count:6 , 50 per page) page: 1

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

No data

Variant related genes	Relation type
EXO1	TF binding region
ENSG00000235990	TF binding region
EXO1	CpG island
ENSG00000235990	CpG island
ENSG00000174371	chromatin interactions
ENSG00000091483	chromatin interactions
CCNE1	miRNA target sites

Extended variants
information (count: 3205 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:3205 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2526698	chr1:242029101-242029102	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs572578896	chr1:242029119-242029120	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs146607328	chr1:242029144-242029145	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs377074162	chr1:242029162-242029163	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs181873729	chr1:242029205-242029206	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs2797602	chr1:242029206-242029207	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs562608039	chr1:242029211-242029212	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs549753479	chr1:242029214-242029215	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs2797601	chr1:242029249-242029250	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs548216236	chr1:242029275-242029276	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs186368664	chr1:242029292-242029293	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs527534286	chr1:242029301-242029302	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs549247120	chr1:242029302-242029303	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs2797600	chr1:242029331-242029332	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs377249182	chr1:242029414-242029415	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs570615256	chr1:242029419-242029420	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs539406125	chr1:242029428-242029429	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs188081413	chr1:242029457-242029458	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs549778173	chr1:242029473-242029474	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs570224121	chr1:242029485-242029486	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs536122498	chr1:242029555-242029556	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs555817326	chr1:242029568-242029569	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs566251850	chr1:242029578-242029579	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs535236411	chr1:242029581-242029582	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs553864868	chr1:242029582-242029583	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs577030943	chr1:242029583-242029584	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs368579952	chr1:242029658-242029659	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs140107446	chr1:242029659-242029660	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs372726661	chr1:242029672-242029673	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs12085137	chr1:242029682-242029683	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs4149941	chr1:242029690-242029691	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs4149942	chr1:242029705-242029706	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs542098778	chr1:242029706-242029707	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs180714360	chr1:242029723-242029724	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs4149943	chr1:242029727-242029728	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs527437563	chr1:242029778-242029779	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs186033921	chr1:242029794-242029795	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs147597043	chr1:242029800-242029801	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs4149944	chr1:242029824-242029825	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs34121929	chr1:242029864-242029865	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs577786219	chr1:242029865-242029866	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs145900626	chr1:242029895-242029896	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs533272234	chr1:242029929-242029930	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs149001934	chr1:242029932-242029933	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs570015488	chr1:242029936-242029937	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs191233619	chr1:242029942-242029943	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs143465250	chr1:242030011-242030012	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs566255049	chr1:242030021-242030022	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs535198503	chr1:242030039-242030040	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs558408748	chr1:242030048-242030049	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:439 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:242012000-242032600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr1:242012200-242044000	Weak transcription	Primary B cells from cord blood	blood
3	chr1:242012400-242060200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr1:242012600-242051600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr1:242012600-242051800	Weak transcription	Duodenum Mucosa	Duodenum
6	chr1:242012800-242054600	Weak transcription	HSMM	muscle
7	chr1:242012800-242056000	Weak transcription	Fetal Intestine Small	intestine
8	chr1:242013000-242053400	Weak transcription	Fetal Lung	lung
9	chr1:242013200-242030000	Weak transcription	NHDF-Ad	bronchial
10	chr1:242013200-242030200	Weak transcription	Fetal Muscle Leg	muscle
11	chr1:242013200-242032400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr1:242013200-242034200	Weak transcription	Brain Germinal Matrix	brain
13	chr1:242013200-242036600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr1:242013200-242038800	Strong transcription	HUES6 Cell Line	embryonic stem cell
15	chr1:242013200-242042000	Weak transcription	HepG2	liver
16	chr1:242013200-242048000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr1:242013200-242053200	Weak transcription	Osteobl	bone
18	chr1:242013200-242056400	Weak transcription	NHLF	lung
19	chr1:242013400-242049400	Weak transcription	Muscle Satellite Cultured Cells	--
20	chr1:242013400-242055800	Strong transcription	HUES64 Cell Line	embryonic stem cell
21	chr1:242013600-242038600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr1:242013600-242039000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr1:242014800-242034400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr1:242015600-242038800	Weak transcription	Fetal Intestine Large	intestine
25	chr1:242015800-242041200	Weak transcription	NHEK	skin
26	chr1:242017000-242053800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
27	chr1:242017400-242031600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
28	chr1:242017800-242038400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr1:242018000-242033400	Weak transcription	Placenta	Placenta
30	chr1:242018000-242046600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr1:242018400-242030200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr1:242018400-242030200	Weak transcription	Thymus	Thymus
33	chr1:242018400-242065600	Weak transcription	Fetal Stomach	stomach
34	chr1:242019400-242037400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
35	chr1:242019600-242037000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr1:242019600-242037400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
37	chr1:242020000-242030400	Weak transcription	Cortex derived primary cultured neurospheres	brain
38	chr1:242020400-242038200	Strong transcription	HUES48 Cell Line	embryonic stem cell
39	chr1:242020800-242037000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr1:242020800-242037000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr1:242020800-242038800	Strong transcription	Dnd41	blood
42	chr1:242021600-242032600	Strong transcription	GM12878-XiMat	blood
43	chr1:242023000-242034800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
44	chr1:242024000-242032400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr1:242024600-242035400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr1:242024600-242043400	Weak transcription	Fetal Muscle Trunk	muscle
47	chr1:242024800-242030200	Weak transcription	NH-A	brain
48	chr1:242025200-242030200	Weak transcription	HMEC	breast
49	chr1:242025200-242030200	Weak transcription	HUVEC	blood vessel
50	chr1:242025200-242035600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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