Variant report

Variant	nsv1014626
Chromosome Location	chr1:168441288-168642731
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2657)
CpG islands
(count:858)
Chromatin interactive
region (count:97)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2657 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:168464753-168465207	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:168543576-168543663	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:168633737-168634000	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:168572797-168573106	HepG2	liver:	n/a	n/a
5	ARID3A	chr1:168460863-168461373	HepG2	liver:	n/a	n/a
6	ARID3A	chr1:168524560-168525457	HepG2	liver:	n/a	n/a
7	ARID3A	chr1:168520860-168521362	HepG2	liver:	n/a	n/a
8	ARID3A	chr1:168596695-168596912	HepG2	liver:	n/a	n/a
9	ARID3A	chr1:168543585-168543670	K562	blood:	n/a	n/a
10	ARID3A	chr1:168515256-168515515	HepG2	liver:	n/a	n/a
11	ATF1	chr1:168532008-168532100	K562	blood:	n/a	n/a
12	ATF1	chr1:168539928-168540010	K562	blood:	n/a	n/a
13	ATF1	chr1:168606674-168606989	K562	blood:	n/a	n/a
14	ATF1	chr1:168561672-168561721	K562	blood:	n/a	n/a
15	ATF1	chr1:168583619-168583840	K562	blood:	n/a	n/a
16	ATF1	chr1:168552815-168552924	K562	blood:	n/a	n/a
17	ATF1	chr1:168557771-168557814	K562	blood:	n/a	n/a
18	ATF1	chr1:168475798-168475937	K562	blood:	n/a	n/a
19	ATF2	chr1:168522954-168523589	GM12878	blood:	n/a	n/a
20	ATF2	chr1:168473680-168474125	GM12878	blood:	n/a	n/a
21	ATF2	chr1:168478943-168479856	GM12878	blood:	n/a	n/a
22	ATF2	chr1:168478928-168479900	GM12878	blood:	n/a	n/a
23	ATF3	chr1:168592406-168592751	K562	blood:	n/a	n/a
24	BATF	chr1:168473685-168473986	GM12878	blood:	n/a	chr1:168473865-168473874
25	BATF	chr1:168541966-168542286	GM12878	blood:	n/a	n/a
26	BATF	chr1:168479004-168479858	GM12878	blood:	n/a	n/a
27	BATF	chr1:168531233-168531559	GM12878	blood:	n/a	n/a
28	BATF	chr1:168481703-168482052	GM12878	blood:	n/a	chr1:168481884-168481895
29	BATF	chr1:168541992-168542278	GM12878	blood:	n/a	n/a
30	BATF	chr1:168473240-168473523	GM12878	blood:	n/a	n/a
31	BATF	chr1:168512256-168512493	GM12878	blood:	n/a	n/a
32	BATF	chr1:168522882-168523633	GM12878	blood:	n/a	chr1:168523293-168523301
33	BATF	chr1:168473277-168473594	GM12878	blood:	n/a	n/a
34	BATF	chr1:168473648-168474136	GM12878	blood:	n/a	chr1:168473865-168473874
35	BATF	chr1:168549541-168549855	GM12878	blood:	n/a	n/a
36	BATF	chr1:168477553-168477861	GM12878	blood:	n/a	n/a
37	BCL11A	chr1:168473645-168473999	GM12878	blood:	n/a	n/a
38	BCL11A	chr1:168522989-168523725	GM12878	blood:	n/a	n/a
39	BCL11A	chr1:168479021-168479870	GM12878	blood:	n/a	chr1:168479236-168479245
40	BCL3	chr1:168479054-168479976	GM12878	blood:	n/a	chr1:168479236-168479245
41	BCLAF1	chr1:168479019-168479933	GM12878	blood:	n/a	chr1:168479236-168479245
42	BCLAF1	chr1:168522955-168523350	GM12878	blood:	n/a	n/a
43	BCLAF1	chr1:168479002-168479857	GM12878	blood:	n/a	chr1:168479236-168479245
44	BHLHE40	chr1:168478593-168480156	GM12878	blood:	n/a	n/a
45	BHLHE40	chr1:168572741-168573102	HepG2	liver:	n/a	n/a
46	BHLHE40	chr1:168583630-168583845	K562	blood:	n/a	n/a
47	BHLHE40	chr1:168522955-168523788	GM12878	blood:	n/a	n/a
48	BHLHE40	chr1:168505012-168505150	GM12878	blood:	n/a	n/a
49	BHLHE40	chr1:168583009-168583236	K562	blood:	n/a	n/a
50	BHLHE40	chr1:168490171-168490475	K562	blood:	n/a	n/a

(count:858 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:168466986-168467036	IMR90	lung:	fetal
2	chr1:168544539-168544589	HMEC	breast:	n/a
3	chr1:168514532-168514582	BE2_C	brain:	n/a
4	chr1:168466986-168467036	ProgFib	skin:	n/a
5	chr1:168466986-168467036	IMR90	lung:	fetal
6	chr1:168544539-168544589	HMEC	breast:	n/a
7	chr1:168514532-168514582	BE2_C	brain:	n/a
8	chr1:168466986-168467036	ProgFib	skin:	n/a
9	chr1:168513310-168513360	ECC-1	luminal epithelium:	n/a
10	chr1:168514532-168514582	HepG2	liver:	n/a
11	chr1:168510365-168510415	SK-N-SH	brain:	n/a
12	chr1:168513067-168513117	SK-N-SH_RA	brain:	n/a
13	chr1:168453196-168453246	HRE	kidney:	n/a
14	chr1:168510169-168510219	SK-N-MC	brain:	n/a
15	chr1:168549490-168549540	BE2_C	brain:	n/a
16	chr1:168466986-168467036	GM19239	blood:	n/a
17	chr1:168510169-168510219	U87	brain:	n/a
18	chr1:168514532-168514582	SAEC	small airway:	n/a
19	chr1:168544874-168544924	ECC-1	luminal epithelium:	n/a
20	chr1:168513242-168513292	MCF10A-Er-Src	breast:	n/a
21	chr1:168544874-168544924	ProgFib	skin:	n/a
22	chr1:168513310-168513360	Hepatocyte	liver:	n/a
23	chr1:168489851-168489901	SAEC	small airway:	n/a
24	chr1:168514532-168514582	HRPEpiC	eye:	n/a
25	chr1:168544539-168544589	RPTEC	kidney:	n/a
26	chr1:168453196-168453246	LNCaP	prostate:	n/a
27	chr1:168514108-168514158	BE2_C	brain:	n/a
28	chr1:168549490-168549540	AoSMC	blood vessel:	n/a
29	chr1:168489851-168489901	HRE	kidney:	n/a
30	chr1:168489851-168489901	T-47D	breast:	n/a
31	chr1:168544539-168544589	AG09319	gingival:	n/a
32	chr1:168513067-168513117	HRCEpiC	kidney:	n/a
33	chr1:168513067-168513117	HRPEpiC	eye:	n/a
34	chr1:168513067-168513117	Jurkat	blood:	n/a
35	chr1:168514108-168514158	Hela-S3	cervix:	n/a
36	chr1:168513242-168513292	HUVEC	blood vessel:	n/a
37	chr1:168513310-168513360	AG10803	skin:	n/a
38	chr1:168513242-168513292	AG09319	gingival:	n/a
39	chr1:168453196-168453246	HepG2	liver:	n/a
40	chr1:168545835-168545885	HCM	heart:	n/a
41	chr1:168453196-168453246	AG04449	skin:	fetal
42	chr1:168510365-168510415	NH-A	brain:	n/a
43	chr1:168513310-168513360	A549	lung:	n/a
44	chr1:168545835-168545885	NB4	blood:	n/a
45	chr1:168514532-168514582	Hela-S3	cervix:	n/a
46	chr1:168544539-168544589	H1-hESC	embryonic stem cell:	embryo
47	chr1:168489851-168489901	NB4	blood:	n/a
48	chr1:168544539-168544589	LNCaP	prostate:	n/a
49	chr1:168489851-168489901	HMEC	breast:	n/a
50	chr1:168510365-168510415	SKMC	muscle:	n/a

(count:97 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:168572459..168573424-chr1:169317442..169318283,3	MCF-7	breast:
2	chr1:168572596..168573422-chr1:169103197..169103848,3	MCF-7	breast:
3	chr1:168483037..168485240-chr1:168486216..168489103,2	MCF-7	breast:
4	chr1:168478358..168480427-chr1:168489705..168492143,2	MCF-7	breast:
5	chr1:168605193..168606024-chr1:169103173..169104078,2	MCF-7	breast:
6	chr1:168470086..168472629-chr1:168474827..168477512,2	K562	blood:
7	chr1:168449934..168452789-chr1:168461978..168463647,2	K562	blood:
8	chr1:168470086..168472629-chr1:168474827..168477512,2	K562	blood:
9	chr1:168582928..168585268-chr1:168586137..168588678,2	K562	blood:
10	chr1:168553388..168555903-chr1:168558533..168560056,2	K562	blood:
11	chr1:168408971..168409658-chr1:168572873..168573377,2	MCF-7	breast:
12	chr1:168474261..168477082-chr1:168484366..168486657,2	MCF-7	breast:
13	chr1:168556383..168558957-chr1:168559815..168561713,2	MCF-7	breast:
14	chr1:168572846..168573369-chr1:168606389..168607281,2	MCF-7	breast:
15	chr1:168556856..168559296-chr1:168559903..168562265,2	K562	blood:
16	chr1:168635367..168638330-chr1:168655240..168657100,2	MCF-7	breast:
17	chr1:168474919..168477092-chr1:168477374..168479574,2	MCF-7	breast:
18	chr1:168578094..168580109-chr1:168583246..168584781,2	MCF-7	breast:
19	chr1:168605717..168608617-chr1:168609502..168611325,2	MCF-7	breast:
20	chr1:168572929..168574536-chr1:169075342..169076920,2	MCF-7	breast:
21	chr1:168496907..168499470-chr1:168500641..168502790,2	K562	blood:
22	chr1:168605717..168608617-chr1:168609502..168611325,2	MCF-7	breast:
23	chr1:168582595..168585268-chr1:168586137..168589627,3	K562	blood:
24	chr1:168421956..168424286-chr1:168536137..168537722,2	K562	blood:
25	chr1:168474261..168477082-chr1:168484366..168486657,2	MCF-7	breast:
26	chr1:168538915..168539776-chr8:141248331..141249019,2	MCF-7	breast:
27	chr1:168474919..168477092-chr1:168477374..168479574,2	MCF-7	breast:
28	chr1:168408738..168409696-chr1:168543083..168544145,4	MCF-7	breast:
29	chr1:168488187..168491038-chr1:168501601..168503776,2	MCF-7	breast:
30	chr1:168587487..168589567-chr1:168600039..168601868,2	K562	blood:
31	chr1:168606300..168607332-chr1:169317339..169318501,5	MCF-7	breast:
32	chr1:168575395..168578133-chr1:169074218..169076866,2	MCF-7	breast:
33	chr1:168472959..168474746-chr1:168475771..168477537,2	MCF-7	breast:
34	chr1:168409048..168409630-chr1:168543648..168544296,2	K562	blood:
35	chr1:168590993..168592623-chr1:168594725..168596497,2	K562	blood:
36	chr1:168530651..168532220-chr1:168536771..168538342,2	K562	blood:
37	chr1:168572434..168572967-chr1:169515424..169516289,2	MCF-7	breast:
38	chr1:168604062..168606034-chr1:169316647..169318325,2	MCF-7	breast:
39	chr1:168146778..168149241-chr1:168497908..168500153,2	K562	blood:
40	chr1:168521001..168522517-chr1:168539526..168541091,2	K562	blood:
41	chr1:168606099..168608125-chr1:168618490..168620719,2	MCF-7	breast:
42	chr1:168613512..168616027-chr1:169073937..169076265,3	MCF-7	breast:
43	chr1:168556856..168559296-chr1:168559903..168562265,2	K562	blood:
44	chr1:168444486..168446892-chr1:168447378..168451317,3	K562	blood:
45	chr1:168572846..168573369-chr1:168606389..168607281,2	MCF-7	breast:
46	chr1:168606099..168608125-chr1:168618490..168620719,2	MCF-7	breast:
47	chr1:168472959..168474746-chr1:168475771..168477537,2	MCF-7	breast:
48	chr1:168572840..168573443-chr1:169680986..169681557,2	MCF-7	breast:
49	chr1:168578094..168580109-chr1:168583246..168584781,2	MCF-7	breast:
50	chr1:168535665..168537230-chr1:168537379..168540147,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-XCL2-3	chr1:168519904-168519973	NONHSAT007439
2	lnc-XCL2-3	chr1:168514595-168514697	NONHSAT007439
3	lnc-XCL2-1	chr1:168454481-168454544	XLOC_001084
4	lnc-XCL2-1	chr1:168464826-168464882	XLOC_001084
5	lnc-XCL2-3	chr1:168507170-168507746	l_145_NR_026957
6	lnc-XCL2-4	chr1:168547891-168548677	NONHSAT007441
7	lnc-XCL2-3	chr1:168514595-168514697	l_145_NR_026957
8	lnc-XCL2-1	chr1:168454811-168454969	XLOC_001084
9	lnc-XCL2-3	chr1:168507532-168507746	NONHSAT007439
10	lnc-XCL2-3	chr1:168509298-168510272	l_145_NR_026957
11	lnc-XCL2-1	chr1:168463284-168463362	XLOC_001084
12	lnc-XCL2-3	chr1:168519904-168519973	l_145_NR_026957

No data

Variant related genes	Relation type
XCL2	TF binding region
ENSG00000227777	TF binding region
ENSG00000237658	TF binding region
XCL1	TF binding region
ENSG00000229757	TF binding region
XCL2	CpG island
ENSG00000227777	CpG island
ENSG00000237658	CpG island
XCL1	CpG island
ENSG00000229757	CpG island
ENSG00000167632	chromatin interactions
ENSG00000205542	chromatin interactions
ENSG00000237658	chromatin interactions
ENSG00000143155	chromatin interactions
ENSG00000143153	chromatin interactions
TRIM2	miRNA target sites
SUMO2	miRNA target sites
KIT	miRNA target sites

Extended variants
information (count: 7641 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:7641 , 50 per page) page: 1 2 3 4 5 6 7 ... 153

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs376993161	chr1:168441290-168441291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs370918563	chr1:168441294-168441295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs374625658	chr1:168441310-168441311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs368337013	chr1:168441312-168441313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs183520239	chr1:168441314-168441315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs186704628	chr1:168441329-168441330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs77851487	chr1:168441355-168441356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs373476582	chr1:168441403-168441404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs191304320	chr1:168441424-168441425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs370750762	chr1:168441440-168441441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs200786471	chr1:168441441-168441442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs202056323	chr1:168441442-168441443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs375216164	chr1:168441447-168441448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs199531943	chr1:168441448-168441449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs532740275	chr1:168441465-168441466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs547718749	chr1:168441538-168441539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs560072507	chr1:168441551-168441552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs530445647	chr1:168441570-168441571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs548575010	chr1:168441575-168441576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs114839790	chr1:168441590-168441591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs537107677	chr1:168441644-168441645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs539122531	chr1:168441646-168441647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs12035479	chr1:168441651-168441652	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs12035480	chr1:168441687-168441688	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs77867708	chr1:168441697-168441698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs150357758	chr1:168441710-168441711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs553582927	chr1:168441765-168441766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs1746250	chr1:168441766-168441767	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs536160673	chr1:168441777-168441778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs533486749	chr1:168441780-168441781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs575992735	chr1:168441788-168441789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs570871752	chr1:168441793-168441794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs564985603	chr1:168441813-168441814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs530538842	chr1:168441819-168441820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs550625422	chr1:168441836-168441837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs567231920	chr1:168441847-168441848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs549982988	chr1:168441865-168441866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs149047708	chr1:168441903-168441904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs143777480	chr1:168441915-168441916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs530384486	chr1:168441929-168441930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs151081306	chr1:168441946-168441947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs184528249	chr1:168441959-168441960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs530930322	chr1:168441964-168441965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs141117410	chr1:168441965-168441966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs558726829	chr1:168441976-168441977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs566774958	chr1:168441984-168441985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs570905620	chr1:168441986-168441987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs78818956	chr1:168441992-168441993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs187811630	chr1:168441993-168441994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs374812282	chr1:168442028-168442029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	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
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	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
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Soft tissue tumor	16732325	CNVD
Cancer	17060936	CNVD
Lung cancer	16740712	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Myelofibrosis	22110671	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Williams-beuren syndrome	16971481	CNVD
Developmental delay	21147756	CNVD
Burkitt''s lymphoma	20823134	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:2113 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:168433800-168443400	Weak transcription	Liver	Liver
2	chr1:168434400-168443600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr1:168435800-168451400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr1:168436400-168441400	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr1:168439200-168450200	Weak transcription	Stomach Smooth Muscle	stomach
6	chr1:168439400-168442600	Weak transcription	Fetal Intestine Large	intestine
7	chr1:168439400-168443400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr1:168439400-168443400	Weak transcription	Spleen	Spleen
9	chr1:168439400-168446200	Weak transcription	Primary T cells fromperipheralblood	blood
10	chr1:168439400-168451400	Weak transcription	Ovary	ovary
11	chr1:168440400-168451200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr1:168440400-168453000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr1:168440600-168442400	Weak transcription	HepG2	liver
14	chr1:168440600-168443200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr1:168440600-168443400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr1:168440600-168445800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
17	chr1:168440600-168445800	Weak transcription	Colon Smooth Muscle	Colon
18	chr1:168440600-168445800	Weak transcription	Placenta Amnion	Placenta Amnion
19	chr1:168440600-168446000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr1:168440600-168446400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
21	chr1:168440800-168443400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr1:168440800-168444200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr1:168442400-168447400	Enhancers	HepG2	liver
24	chr1:168442600-168444200	Enhancers	Fetal Intestine Large	intestine
25	chr1:168443000-168443200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr1:168443200-168443600	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
27	chr1:168443400-168444000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr1:168443400-168444000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr1:168443400-168444200	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr1:168443400-168444200	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr1:168443400-168444200	ZNF genes & repeats	Liver	Liver
32	chr1:168443400-168444200	ZNF genes & repeats	Spleen	Spleen
33	chr1:168443600-168444000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
34	chr1:168443600-168444200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr1:168443600-168445800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
36	chr1:168444000-168449800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr1:168444000-168450200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr1:168444000-168451400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr1:168444200-168444400	Weak transcription	Right Ventricle	heart
40	chr1:168444200-168444600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr1:168444200-168445000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr1:168444200-168445800	Weak transcription	Fetal Intestine Large	intestine
43	chr1:168444200-168446000	Weak transcription	Spleen	Spleen
44	chr1:168444200-168450400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr1:168444200-168450400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr1:168444200-168461000	Weak transcription	Liver	Liver
47	chr1:168444600-168445800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr1:168445000-168445200	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr1:168445000-168445600	Enhancers	NHEK	skin
50	chr1:168445000-168446000	Enhancers	HMEC	breast

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