Variant report

Variant	nsv508703
Chromosome Location	chr1:242146940-242252101
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1505)
CpG islands
(count:1161)
Chromatin interactive
region (count:40)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1505 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:242149085-242149421	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:242183160-242183497	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:242183142-242183615	K562	blood:	n/a	n/a
4	ARID3A	chr1:242149175-242149484	K562	blood:	n/a	n/a
5	ATF1	chr1:242183166-242183478	K562	blood:	n/a	n/a
6	ATF1	chr1:242200610-242200626	K562	blood:	n/a	n/a
7	ATF1	chr1:242147616-242147938	K562	blood:	n/a	n/a
8	ATF1	chr1:242172320-242172434	K562	blood:	n/a	n/a
9	ATF2	chr1:242161604-242162019	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr1:242161623-242162128	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF3	chr1:242153332-242153616	K562	blood:	n/a	n/a
12	BACH1	chr1:242229314-242229325	K562	blood:	n/a	n/a
13	BACH1	chr1:242161817-242162371	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr1:242198202-242198218	K562	blood:	n/a	n/a
15	BATF	chr1:242221934-242222160	GM12878	blood:	n/a	n/a
16	BATF	chr1:242152456-242152709	GM12878	blood:	n/a	n/a
17	BCL11A	chr1:242152382-242152691	GM12878	blood:	n/a	n/a
18	BCL3	chr1:242161617-242162295	A549	lung:	n/a	n/a
19	BCL3	chr1:242161671-242162382	A549	lung:	n/a	n/a
20	BHLHE40	chr1:242180986-242181269	K562	blood:	n/a	n/a
21	BHLHE40	chr1:242181058-242181232	GM12878	blood:	n/a	n/a
22	BHLHE40	chr1:242153309-242153692	K562	blood:	n/a	chr1:242153473-242153482 chr1:242153473-242153482 chr1:242153467-242153488 chr1:242153472-242153481
23	BHLHE40	chr1:242161685-242162227	K562	blood:	n/a	chr1:242162042-242162058
24	BHLHE40	chr1:242187226-242187277	GM12878	blood:	n/a	n/a
25	BHLHE40	chr1:242152479-242152805	GM12878	blood:	n/a	n/a
26	BRCA1	chr1:242161887-242162178	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr1:242169360-242169754	Hela-S3	cervix:	n/a	n/a
28	CBX3	chr1:242161587-242162212	K562	blood:	n/a	n/a
29	CBX3	chr1:242161511-242162367	HCT-116	colon:	n/a	n/a
30	CBX3	chr1:242147583-242147949	K562	blood:	n/a	n/a
31	CBX3	chr1:242161494-242162370	HCT-116	colon:	n/a	n/a
32	CBX3	chr1:242161655-242162161	K562	blood:	n/a	n/a
33	CCNT2	chr1:242161625-242162175	K562	blood:	n/a	chr1:242162035-242162044
34	CEBPB	chr1:242179739-242180095	MCF-7	breast:	n/a	chr1:242179902-242179915 chr1:242179902-242179915 chr1:242179904-242179913 chr1:242179901-242179918 chr1:242179904-242179913 chr1:242179904-242179913 chr1:242179902-242179913 chr1:242179904-242179913 chr1:242179902-242179915 chr1:242179903-242179914 chr1:242179902-242179913
35	CEBPB	chr1:242179759-242180079	K562	blood:	n/a	chr1:242179902-242179915 chr1:242179902-242179915 chr1:242179904-242179913 chr1:242179901-242179918 chr1:242179904-242179913 chr1:242179904-242179913 chr1:242179902-242179913 chr1:242179904-242179913 chr1:242179902-242179915 chr1:242179903-242179914 chr1:242179902-242179913
36	CEBPB	chr1:242189149-242189433	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr1:242206535-242206783	A549	lung:	n/a	n/a
38	CEBPB	chr1:242228014-242228271	HepG2	liver:	n/a	chr1:242228085-242228096
39	CEBPB	chr1:242189134-242189468	K562	blood:	n/a	n/a
40	CEBPB	chr1:242189134-242189456	HepG2	liver:	n/a	n/a
41	CEBPB	chr1:242206531-242206752	HepG2	liver:	n/a	n/a
42	CEBPB	chr1:242179719-242180100	K562	blood:	n/a	chr1:242179902-242179915 chr1:242179902-242179915 chr1:242179904-242179913 chr1:242179901-242179918 chr1:242179904-242179913 chr1:242179904-242179913 chr1:242179902-242179913 chr1:242179904-242179913 chr1:242179902-242179915 chr1:242179903-242179914 chr1:242179902-242179913
43	CEBPB	chr1:242188213-242188413	K562	blood:	n/a	chr1:242188320-242188331
44	CEBPB	chr1:242179726-242180075	HepG2	liver:	n/a	chr1:242179902-242179915 chr1:242179902-242179915 chr1:242179904-242179913 chr1:242179901-242179918 chr1:242179904-242179913 chr1:242179904-242179913 chr1:242179902-242179913 chr1:242179904-242179913 chr1:242179902-242179915 chr1:242179903-242179914 chr1:242179902-242179913
45	CEBPB	chr1:242152115-242152827	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr1:242206615-242206735	K562	blood:	n/a	n/a
47	CEBPB	chr1:242231304-242231681	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr1:242188242-242188430	IMR90	lung:	n/a	chr1:242188320-242188331
49	CEBPB	chr1:242156009-242156368	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr1:242188199-242188401	HepG2	liver:	n/a	chr1:242188320-242188331

(count:1161 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:242217440-242217490	AG09319	gingival:	n/a
2	chr1:242222868-242222918	AoSMC	blood vessel:	n/a
3	chr1:242217440-242217490	AG09319	gingival:	n/a
4	chr1:242222868-242222918	AoSMC	blood vessel:	n/a
5	chr1:242161806-242161856	AG04449	skin:	fetal
6	chr1:242163388-242163438	HCM	heart:	n/a
7	chr1:242224772-242224822	SK-N-SH_RA	brain:	n/a
8	chr1:242220538-242220588	RPTEC	kidney:	n/a
9	chr1:242220925-242220975	SK-N-MC	brain:	n/a
10	chr1:242220538-242220588	GM12878	blood:	n/a
11	chr1:242162828-242162878	SK-N-SH	brain:	n/a
12	chr1:242163388-242163438	NT2-D1	testis:	n/a
13	chr1:242161881-242161931	T-47D	breast:	n/a
14	chr1:242220925-242220975	HRCEpiC	kidney:	n/a
15	chr1:242162802-242162852	HPAEpiC	pulmonary alveolar:	n/a
16	chr1:242220925-242220975	HCF	heart:	n/a
17	chr1:242220301-242220351	U87	brain:	n/a
18	chr1:242220538-242220588	GM19239	blood:	n/a
19	chr1:242219141-242219191	LNCaP	prostate:	n/a
20	chr1:242220925-242220975	NH-A	brain:	n/a
21	chr1:242161881-242161931	NB4	blood:	n/a
22	chr1:242162802-242162852	Jurkat	blood:	n/a
23	chr1:242218597-242218647	HCF	heart:	n/a
24	chr1:242220301-242220351	PrEC	prostate:	n/a
25	chr1:242217440-242217490	PFSK-1	brain:	n/a
26	chr1:242161780-242161830	IMR90	lung:	fetal
27	chr1:242163517-242163567	GM19239	blood:	n/a
28	chr1:242162828-242162878	PrEC	prostate:	n/a
29	chr1:242161881-242161931	GM12878	blood:	n/a
30	chr1:242220475-242220525	NHBE	bronchial:	n/a
31	chr1:242162802-242162852	HCF	heart:	n/a
32	chr1:242161806-242161856	HEEpiC	esophagus:	n/a
33	chr1:242163517-242163567	HCPEpiC	choroid plexus:	n/a
34	chr1:242219141-242219191	HRCEpiC	kidney:	n/a
35	chr1:242159456-242159506	MCF10A-Er-Src	breast:	n/a
36	chr1:242161881-242161931	PrEC	prostate:	n/a
37	chr1:242161780-242161830	ProgFib	skin:	n/a
38	chr1:242220925-242220975	ProgFib	skin:	n/a
39	chr1:242222868-242222918	GM06990	blood:	n/a
40	chr1:242161806-242161856	HCM	heart:	n/a
41	chr1:242163517-242163567	Hepatocyte	liver:	n/a
42	chr1:242220475-242220525	H1-hESC	embryonic stem cell:	embryo
43	chr1:242250508-242250558	HRE	kidney:	n/a
44	chr1:242159456-242159506	Jurkat	blood:	n/a
45	chr1:242163388-242163438	HCPEpiC	choroid plexus:	n/a
46	chr1:242220475-242220525	PFSK-1	brain:	n/a
47	chr1:242250508-242250558	ECC-1	luminal epithelium:	n/a
48	chr1:242219141-242219191	HCF	heart:	n/a
49	chr1:242217440-242217490	CMK	blood:	n/a
50	chr1:242217440-242217490	HepG2	liver:	n/a

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:242161372..242162202-chr1:242171638..242172445,2	K562	blood:
2	chr1:242060961..242063036-chr1:242175225..242177165,2	K562	blood:
3	chr1:242242880..242245765-chr1:242247540..242249469,2	K562	blood:
4	chr1:242192385..242195327-chr1:242197724..242199725,2	K562	blood:
5	chr1:242217500..242220203-chr1:242220898..242222680,2	K562	blood:
6	chr1:242161372..242162202-chr1:242171638..242172445,2	K562	blood:
7	chr1:242120814..242121654-chr1:242161517..242162480,3	MCF-7	breast:
8	chr1:242182508..242183674-chr1:242292156..242293080,6	MCF-7	breast:
9	chr1:242235938..242237964-chr1:242241815..242244808,2	K562	blood:
10	chr1:241694305..241695206-chr1:242161362..242162044,2	K562	blood:
11	chr1:242059673..242060311-chr1:242149546..242150431,2	MCF-7	breast:
12	chr1:242144580..242146530-chr1:242152140..242153827,2	K562	blood:
13	chr1:242059613..242060290-chr1:242179713..242180384,2	MCF-7	breast:
14	chr1:241052705..241053405-chr1:242180887..242181830,2	K562	blood:
15	chr1:242182892..242183793-chr1:242638283..242638859,2	MCF-7	breast:
16	chr1:242120855..242121405-chr1:242149313..242150082,2	MCF-7	breast:
17	chr1:242059414..242060329-chr1:242180301..242181638,4	K562	blood:
18	chr1:241694184..241695730-chr1:242145323..242147944,2	K562	blood:
19	chr1:242242880..242245765-chr1:242247540..242249469,2	K562	blood:
20	chr1:242059371..242060335-chr1:242161395..242162231,4	MCF-7	breast:
21	chr1:242121060..242121703-chr1:242148791..242149743,4	MCF-7	breast:
22	chr1:242063761..242065381-chr1:242152078..242153652,2	MCF-7	breast:
23	chr1:241774175..241774917-chr1:242161594..242162291,2	K562	blood:
24	chr1:242248261..242249840-chr1:242272040..242274388,2	K562	blood:
25	chr1:241768518..241769062-chr1:242180915..242181517,2	MCF-7	breast:
26	chr1:242059480..242060334-chr1:242148747..242149804,4	K562	blood:
27	chr1:242217500..242220203-chr1:242220898..242222680,2	K562	blood:
28	chr1:242171965..242174414-chr1:242186274..242187962,2	K562	blood:
29	chr1:242186609..242188797-chr1:242246316..242249204,2	K562	blood:
30	chr1:241774394..241774939-chr1:242180635..242181533,2	K562	blood:
31	chr1:241774407..241775239-chr1:242148964..242149557,2	MCF-7	breast:
32	chr1:242120900..242121506-chr1:242180828..242181412,2	MCF-7	breast:
33	chr1:242235938..242237964-chr1:242241815..242244808,2	K562	blood:
34	chr1:241774424..241775122-chr1:242161574..242162262,2	MCF-7	breast:
35	chr1:242059401..242060332-chr1:242161246..242162002,4	K562	blood:
36	chr1:242192385..242195327-chr1:242197724..242199725,2	K562	blood:
37	chr1:242219802..242221772-chr1:242224565..242228603,3	MCF-7	breast:
38	chr1:242059788..242060336-chr1:242180683..242181366,2	MCF-7	breast:
39	chr1:242183008..242183632-chr1:242588513..242589035,2	MCF-7	breast:
40	chr1:242059370..242060370-chr1:242148860..242150209,7	MCF-7	breast:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EXO1-8	chr1:242147327-242147451	NONHSAT010559
2	lnc-EXO1-8	chr1:242234983-242235083	ucscGeneNc_uc001iac_2
3	lnc-EXO1-8	chr1:242233308-242233425	NONHSAT010559
4	lnc-EXO1-8	chr1:242208335-242208444	NONHSAT010559
5	lnc-EXO1-8	chr1:242234983-242235083	NONHSAT010559
6	lnc-EXO1-8	chr1:242240622-242240845	NONHSAT010559
7	lnc-EXO1-8	chr1:242208335-242208444	ucscGeneNc_uc001iac_2
8	lnc-EXO1-8	chr1:242233308-242233425	ucscGeneNc_uc001iac_2
9	lnc-EXO1-8	chr1:242147327-242147451	ucscGeneNc_uc001iac_2
10	lnc-EXO1-8	chr1:242239946-242240017	NONHSAT010559
11	lnc-EXO1-8	chr1:242239946-242240017	ucscGeneNc_uc001iac_2
12	lnc-EXO1-8	chr1:242240622-242240845	ucscGeneNc_uc001iac_2

No data

Variant related genes	Relation type
CFL1P4	TF binding region
RNU6-1139P	TF binding region
MAP1LC3C	TF binding region
TUBB8P6	TF binding region
CFL1P4	CpG island
RNU6-1139P	CpG island
MAP1LC3C	CpG island
TUBB8P6	CpG island
ENSG00000117009	chromatin interactions
ENSG00000196289	chromatin interactions
ENSG00000224625	chromatin interactions
ENSG00000223119	chromatin interactions

Extended variants
information (count: 3962 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:3962 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs377371812	chr1:242146957-242146958	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs572600398	chr1:242147009-242147010	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs541222297	chr1:242147026-242147027	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs564383334	chr1:242147027-242147028	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs533505768	chr1:242147050-242147051	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs73141722	chr1:242147103-242147104	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs563699097	chr1:242147130-242147131	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs529597420	chr1:242147131-242147132	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs145444447	chr1:242147136-242147137	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs148399339	chr1:242147142-242147143	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs375102436	chr1:242147153-242147154	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs111354429	chr1:242147176-242147177	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs28488349	chr1:242147180-242147181	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs28578531	chr1:242147187-242147188	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs192431901	chr1:242147261-242147262	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs112927743	chr1:242147310-242147311	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs184569101	chr1:242147316-242147317	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs539195959	chr1:242147321-242147322	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs189405437	chr1:242147334-242147335	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
20	rs569274171	chr1:242147340-242147341	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
21	rs191102734	chr1:242147356-242147357	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
22	rs371610347	chr1:242147365-242147366	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
23	rs112303112	chr1:242147420-242147421	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
24	rs184390349	chr1:242147499-242147500	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs572312096	chr1:242147543-242147544	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs142211983	chr1:242147563-242147564	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs558031159	chr1:242147602-242147603	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs578127753	chr1:242147639-242147640	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs543967048	chr1:242147723-242147724	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs386641217	chr1:242147770-242147771	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs116799652	chr1:242147775-242147776	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs114067037	chr1:242147776-242147777	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs28482794	chr1:242147779-242147780	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs28435820	chr1:242147783-242147784	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs551682585	chr1:242147845-242147846	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs189809834	chr1:242147853-242147854	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs532850691	chr1:242147869-242147870	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs549436246	chr1:242147874-242147875	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs539524772	chr1:242147877-242147878	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs535064836	chr1:242147892-242147893	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs370029274	chr1:242147895-242147896	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs145913311	chr1:242147908-242147909	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs572536130	chr1:242147939-242147940	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs371790164	chr1:242147940-242147941	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs147851502	chr1:242147982-242147983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs564750704	chr1:242147983-242147984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs28693018	chr1:242147995-242147996	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs28687585	chr1:242148017-242148018	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs28707795	chr1:242148038-242148039	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs74151092	chr1:242148039-242148040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

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
Acute lymphoblastic leukemia	21339820	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:608 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:242121400-242161800	Weak transcription	Right Atrium	heart
2	chr1:242137200-242153200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr1:242142800-242153400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr1:242149400-242149600	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr1:242149400-242149800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr1:242149600-242149800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr1:242149600-242155600	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr1:242149800-242151600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr1:242150400-242152200	Weak transcription	A549	lung
10	chr1:242151400-242153600	Enhancers	Cortex derived primary cultured neurospheres	brain
11	chr1:242151600-242152400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr1:242151600-242152400	Enhancers	Hela-S3	cervix
13	chr1:242151600-242152600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr1:242151600-242152600	Enhancers	Adipose Nuclei	Adipose
15	chr1:242151600-242152600	Enhancers	Brain Germinal Matrix	brain
16	chr1:242151600-242153000	Enhancers	Fetal Kidney	kidney
17	chr1:242151600-242153600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr1:242151600-242153600	Enhancers	Fetal Lung	lung
19	chr1:242151600-242153600	Enhancers	NH-A	brain
20	chr1:242151600-242154400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr1:242151600-242154400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr1:242151600-242154400	Enhancers	HSMM	muscle
23	chr1:242151600-242154600	Enhancers	Fetal Muscle Leg	muscle
24	chr1:242151800-242152000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr1:242151800-242152400	Enhancers	Fetal Muscle Trunk	muscle
26	chr1:242151800-242153000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr1:242152000-242152400	Enhancers	Colon Smooth Muscle	Colon
28	chr1:242152000-242154400	Enhancers	Ovary	ovary
29	chr1:242152000-242156600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr1:242152200-242152600	Enhancers	Brain Hippocampus Middle	brain
31	chr1:242152200-242153000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr1:242152200-242153000	Enhancers	HSMMtube	muscle
33	chr1:242152200-242153000	Enhancers	Osteobl	bone
34	chr1:242152200-242154000	Enhancers	A549	lung
35	chr1:242152200-242154200	Enhancers	Muscle Satellite Cultured Cells	--
36	chr1:242152400-242152600	Enhancers	Placenta	Placenta
37	chr1:242152400-242152800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr1:242152400-242152800	Weak transcription	Fetal Muscle Trunk	muscle
39	chr1:242152400-242153000	Flanking Active TSS	Hela-S3	cervix
40	chr1:242152400-242153000	Enhancers	NHLF	lung
41	chr1:242152400-242153600	Enhancers	Fetal Stomach	stomach
42	chr1:242152400-242154200	Enhancers	NHDF-Ad	bronchial
43	chr1:242152600-242156600	Weak transcription	Placenta	Placenta
44	chr1:242152600-242161400	Weak transcription	Adipose Nuclei	Adipose
45	chr1:242152600-242161600	Weak transcription	Brain Germinal Matrix	brain
46	chr1:242152800-242154400	Enhancers	Fetal Muscle Trunk	muscle
47	chr1:242153000-242154800	Enhancers	Hela-S3	cervix
48	chr1:242153000-242156200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr1:242153200-242153400	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr1:242153400-242154400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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