Variant report

Variant	nsv535197
Chromosome Location	chr1:168441488-168642592
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2657)
CpG islands
(count:857)
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	chr1:168543585-168543670	K562	blood:	n/a	n/a
2	ARID3A	chr1:168543576-168543663	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:168464753-168465207	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:168520860-168521362	HepG2	liver:	n/a	n/a
5	ARID3A	chr1:168524560-168525457	HepG2	liver:	n/a	n/a
6	ARID3A	chr1:168596695-168596912	HepG2	liver:	n/a	n/a
7	ARID3A	chr1:168460863-168461373	HepG2	liver:	n/a	n/a
8	ARID3A	chr1:168633737-168634000	HepG2	liver:	n/a	n/a
9	ARID3A	chr1:168515256-168515515	HepG2	liver:	n/a	n/a
10	ARID3A	chr1:168572797-168573106	HepG2	liver:	n/a	n/a
11	ATF1	chr1:168583619-168583840	K562	blood:	n/a	n/a
12	ATF1	chr1:168539928-168540010	K562	blood:	n/a	n/a
13	ATF1	chr1:168557771-168557814	K562	blood:	n/a	n/a
14	ATF1	chr1:168475798-168475937	K562	blood:	n/a	n/a
15	ATF1	chr1:168606674-168606989	K562	blood:	n/a	n/a
16	ATF1	chr1:168561672-168561721	K562	blood:	n/a	n/a
17	ATF1	chr1:168532008-168532100	K562	blood:	n/a	n/a
18	ATF1	chr1:168552815-168552924	K562	blood:	n/a	n/a
19	ATF2	chr1:168478943-168479856	GM12878	blood:	n/a	n/a
20	ATF2	chr1:168522954-168523589	GM12878	blood:	n/a	n/a
21	ATF2	chr1:168478928-168479900	GM12878	blood:	n/a	n/a
22	ATF2	chr1:168473680-168474125	GM12878	blood:	n/a	n/a
23	ATF3	chr1:168592406-168592751	K562	blood:	n/a	n/a
24	BATF	chr1:168481703-168482052	GM12878	blood:	n/a	chr1:168481884-168481895
25	BATF	chr1:168541966-168542286	GM12878	blood:	n/a	n/a
26	BATF	chr1:168473240-168473523	GM12878	blood:	n/a	n/a
27	BATF	chr1:168473277-168473594	GM12878	blood:	n/a	n/a
28	BATF	chr1:168473648-168474136	GM12878	blood:	n/a	chr1:168473865-168473874
29	BATF	chr1:168531233-168531559	GM12878	blood:	n/a	n/a
30	BATF	chr1:168479004-168479858	GM12878	blood:	n/a	n/a
31	BATF	chr1:168477553-168477861	GM12878	blood:	n/a	n/a
32	BATF	chr1:168473685-168473986	GM12878	blood:	n/a	chr1:168473865-168473874
33	BATF	chr1:168549541-168549855	GM12878	blood:	n/a	n/a
34	BATF	chr1:168522882-168523633	GM12878	blood:	n/a	chr1:168523293-168523301
35	BATF	chr1:168541992-168542278	GM12878	blood:	n/a	n/a
36	BATF	chr1:168512256-168512493	GM12878	blood:	n/a	n/a
37	BCL11A	chr1:168479021-168479870	GM12878	blood:	n/a	chr1:168479236-168479245
38	BCL11A	chr1:168522989-168523725	GM12878	blood:	n/a	n/a
39	BCL11A	chr1:168473645-168473999	GM12878	blood:	n/a	n/a
40	BCL3	chr1:168479054-168479976	GM12878	blood:	n/a	chr1:168479236-168479245
41	BCLAF1	chr1:168522955-168523350	GM12878	blood:	n/a	n/a
42	BCLAF1	chr1:168479002-168479857	GM12878	blood:	n/a	chr1:168479236-168479245
43	BCLAF1	chr1:168479019-168479933	GM12878	blood:	n/a	chr1:168479236-168479245
44	BHLHE40	chr1:168505012-168505150	GM12878	blood:	n/a	n/a
45	BHLHE40	chr1:168542032-168542239	GM12878	blood:	n/a	n/a
46	BHLHE40	chr1:168445800-168446148	HepG2	liver:	n/a	n/a
47	BHLHE40	chr1:168572741-168573102	HepG2	liver:	n/a	n/a
48	BHLHE40	chr1:168522955-168523788	GM12878	blood:	n/a	n/a
49	BHLHE40	chr1:168526869-168527242	GM12878	blood:	n/a	n/a
50	BHLHE40	chr1:168583009-168583236	K562	blood:	n/a	n/a

(count:857 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:168489851-168489901	HEK293	kidney:	embryo
2	chr1:168514532-168514582	PrEC	prostate:	n/a
3	chr1:168466986-168467036	SKMC	muscle:	n/a
4	chr1:168489851-168489901	HEK293	kidney:	embryo
5	chr1:168514532-168514582	PrEC	prostate:	n/a
6	chr1:168466986-168467036	SKMC	muscle:	n/a
7	chr1:168466986-168467036	A549	lung:	n/a
8	chr1:168513310-168513360	HUVEC	blood vessel:	n/a
9	chr1:168513242-168513292	RPTEC	kidney:	n/a
10	chr1:168514532-168514582	AG09319	gingival:	n/a
11	chr1:168453196-168453246	HepG2	liver:	n/a
12	chr1:168549490-168549540	Jurkat	blood:	n/a
13	chr1:168549490-168549540	AG04449	skin:	fetal
14	chr1:168514532-168514582	HRE	kidney:	n/a
15	chr1:168544874-168544924	NB4	blood:	n/a
16	chr1:168466986-168467036	NB4	blood:	n/a
17	chr1:168489851-168489901	SK-N-MC	brain:	n/a
18	chr1:168545835-168545885	AG10803	skin:	n/a
19	chr1:168489851-168489901	PANC-1	pancreas:	n/a
20	chr1:168514108-168514158	MCF-7	breast:	n/a
21	chr1:168489851-168489901	RPTEC	kidney:	n/a
22	chr1:168510169-168510219	GM12878	blood:	n/a
23	chr1:168513310-168513360	HEEpiC	esophagus:	n/a
24	chr1:168510365-168510415	HCT-116	colon:	n/a
25	chr1:168453196-168453246	NB4	blood:	n/a
26	chr1:168510169-168510219	Hepatocyte	liver:	n/a
27	chr1:168466986-168467036	PFSK-1	brain:	n/a
28	chr1:168544874-168544924	AG04450	lung:	fetal
29	chr1:168513242-168513292	CMK	blood:	n/a
30	chr1:168514108-168514158	CMK	blood:	n/a
31	chr1:168513242-168513292	ECC-1	luminal epithelium:	n/a
32	chr1:168489851-168489901	HRPEpiC	eye:	n/a
33	chr1:168549490-168549540	AG04450	lung:	fetal
34	chr1:168453196-168453246	SAEC	small airway:	n/a
35	chr1:168549490-168549540	NHDF-neo	bronchial:	n/a
36	chr1:168489851-168489901	LNCaP	prostate:	n/a
37	chr1:168489851-168489901	K562	blood:	n/a
38	chr1:168510365-168510415	T-47D	breast:	n/a
39	chr1:168513067-168513117	Hela-S3	cervix:	n/a
40	chr1:168513067-168513117	MCF-7	breast:	n/a
41	chr1:168513067-168513117	HIPEpiC	eye:	n/a
42	chr1:168466986-168467036	HUVEC	blood vessel:	n/a
43	chr1:168489851-168489901	HEEpiC	esophagus:	n/a
44	chr1:168514108-168514158	HCM	heart:	n/a
45	chr1:168549490-168549540	BE2_C	brain:	n/a
46	chr1:168513067-168513117	SKMC	muscle:	n/a
47	chr1:168510169-168510219	HCPEpiC	choroid plexus:	n/a
48	chr1:168489851-168489901	GM12892	blood:	n/a
49	chr1:168510169-168510219	HL-60	blood:	n/a
50	chr1:168453196-168453246	RPTEC	kidney:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr1:168590993..168592623-chr1:168594725..168596497,2	K562	blood:
2	chr1:168624620..168626985-chr1:169073716..169075620,2	MCF-7	breast:
3	chr1:168553388..168555903-chr1:168558533..168560056,2	K562	blood:
4	chr1:168635367..168638330-chr1:168655240..168657100,2	MCF-7	breast:
5	chr1:168582595..168585268-chr1:168586137..168589627,3	K562	blood:
6	chr1:168605717..168608617-chr1:168609502..168611325,2	MCF-7	breast:
7	chr1:168486143..168488411-chr1:168503326..168505686,2	K562	blood:
8	chr1:168613512..168616027-chr1:169073937..169076265,3	MCF-7	breast:
9	chr1:168482813..168484506-chr1:168493897..168495817,2	K562	blood:
10	chr1:168408971..168409658-chr1:168572873..168573377,2	MCF-7	breast:
11	chr1:168605193..168606024-chr1:169103173..169104078,2	MCF-7	breast:
12	chr1:168535665..168537230-chr1:168537379..168540147,2	MCF-7	breast:
13	chr1:168590882..168592754-chr1:168594350..168596056,2	MCF-7	breast:
14	chr1:168408738..168409696-chr1:168543083..168544145,4	MCF-7	breast:
15	chr1:168556856..168559296-chr1:168559903..168562265,2	K562	blood:
16	chr1:168575395..168578133-chr1:169074218..169076866,2	MCF-7	breast:
17	chr1:168572454..168573380-chr1:169317397..169317940,2	K562	blood:
18	chr1:168605284..168605980-chr1:168956282..168957205,2	MCF-7	breast:
19	chr1:168433780..168435453-chr1:168450998..168452951,2	MCF-7	breast:
20	chr1:168604931..168606716-chr1:169074466..169076968,2	MCF-7	breast:
21	chr1:168406270..168408708-chr1:168577956..168579929,2	MCF-7	breast:
22	chr1:168449934..168452789-chr1:168461978..168463647,2	K562	blood:
23	chr1:168530651..168532220-chr1:168536771..168538342,2	K562	blood:
24	chr1:168607280..168610004-chr1:169101747..169103897,2	MCF-7	breast:
25	chr1:168572434..168572967-chr1:169515424..169516289,2	MCF-7	breast:
26	chr1:168606099..168608125-chr1:168618490..168620719,2	MCF-7	breast:
27	chr1:168449934..168452789-chr1:168461978..168463647,2	K562	blood:
28	chr1:168581005..168585342-chr1:168586418..168588531,4	MCF-7	breast:
29	chr1:168470086..168472629-chr1:168474827..168477512,2	K562	blood:
30	chr1:168582928..168585268-chr1:168586137..168588678,2	K562	blood:
31	chr1:168605132..168606019-chr1:169317390..169318347,3	MCF-7	breast:
32	chr1:168572846..168573369-chr1:168606389..168607281,2	MCF-7	breast:
33	chr1:168578094..168580109-chr1:168583246..168584781,2	MCF-7	breast:
34	chr1:168434236..168435916-chr1:168440122..168441908,2	K562	blood:
35	chr1:168587487..168589567-chr1:168600039..168601868,2	K562	blood:
36	chr1:168572846..168573369-chr1:168606389..168607281,2	MCF-7	breast:
37	chr1:168572446..168573392-chr1:169317346..169318310,9	MCF-7	breast:
38	chr1:168421956..168424286-chr1:168536137..168537722,2	K562	blood:
39	chr1:168582928..168585268-chr1:168586137..168588678,2	K562	blood:
40	chr1:168488187..168491038-chr1:168501601..168503776,2	MCF-7	breast:
41	chr1:168461061..168463419-chr1:168464671..168466571,2	MCF-7	breast:
42	chr1:168483037..168485240-chr1:168486216..168489103,2	MCF-7	breast:
43	chr1:168590882..168592754-chr1:168594350..168596056,2	MCF-7	breast:
44	chr1:168581005..168585342-chr1:168586418..168588531,4	MCF-7	breast:
45	chr1:168478358..168480427-chr1:168489705..168492143,2	MCF-7	breast:
46	chr1:168483037..168485240-chr1:168486216..168489103,2	MCF-7	breast:
47	chr1:168604062..168606034-chr1:169316647..169318325,2	MCF-7	breast:
48	chr1:168478358..168480427-chr1:168489705..168492143,2	MCF-7	breast:
49	chr1:168556856..168559296-chr1:168559903..168562265,2	K562	blood:
50	chr1:168521001..168522517-chr1:168539526..168541091,2	K562	blood:

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

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

No data

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

Extended variants
information (count: 7619 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:7619 , 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	rs547718749	chr1:168441538-168441539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs560072507	chr1:168441551-168441552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs530445647	chr1:168441570-168441571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs548575010	chr1:168441575-168441576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs114839790	chr1:168441590-168441591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs537107677	chr1:168441644-168441645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs539122531	chr1:168441646-168441647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs12035479	chr1:168441651-168441652	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs12035480	chr1:168441687-168441688	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs77867708	chr1:168441697-168441698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs150357758	chr1:168441710-168441711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs553582927	chr1:168441765-168441766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs1746250	chr1:168441766-168441767	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs536160673	chr1:168441777-168441778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs533486749	chr1:168441780-168441781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs575992735	chr1:168441788-168441789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs570871752	chr1:168441793-168441794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs564985603	chr1:168441813-168441814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs530538842	chr1:168441819-168441820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs550625422	chr1:168441836-168441837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs567231920	chr1:168441847-168441848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs549982988	chr1:168441865-168441866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs149047708	chr1:168441903-168441904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs143777480	chr1:168441915-168441916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs530384486	chr1:168441929-168441930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs151081306	chr1:168441946-168441947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs184528249	chr1:168441959-168441960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs530930322	chr1:168441964-168441965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs141117410	chr1:168441965-168441966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs558726829	chr1:168441976-168441977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs566774958	chr1:168441984-168441985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs570905620	chr1:168441986-168441987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs78818956	chr1:168441992-168441993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs187811630	chr1:168441993-168441994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs374812282	chr1:168442028-168442029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs565551924	chr1:168442030-168442031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs192915910	chr1:168442079-168442080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs185138579	chr1:168442092-168442093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs201369779	chr1:168442105-168442106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs537037533	chr1:168442113-168442114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs558297867	chr1:168442115-168442116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs576843932	chr1:168442124-168442125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs79114161	chr1:168442131-168442132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs12133950	chr1:168442132-168442133	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs575088894	chr1:168442144-168442145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs189081221	chr1:168442146-168442147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs537029684	chr1:168442161-168442162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs77800949	chr1:168442163-168442164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs398089647	chr1:168442167-168442168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs563997928	chr1:168442188-168442189	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:2110 , 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	chr1:168439200-168450200	Weak transcription	Stomach Smooth Muscle	stomach
5	chr1:168439400-168442600	Weak transcription	Fetal Intestine Large	intestine
6	chr1:168439400-168443400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr1:168439400-168443400	Weak transcription	Spleen	Spleen
8	chr1:168439400-168446200	Weak transcription	Primary T cells fromperipheralblood	blood
9	chr1:168439400-168451400	Weak transcription	Ovary	ovary
10	chr1:168440400-168451200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr1:168440400-168453000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
12	chr1:168440600-168442400	Weak transcription	HepG2	liver
13	chr1:168440600-168443200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr1:168440600-168443400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr1:168440600-168445800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
16	chr1:168440600-168445800	Weak transcription	Colon Smooth Muscle	Colon
17	chr1:168440600-168445800	Weak transcription	Placenta Amnion	Placenta Amnion
18	chr1:168440600-168446000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr1:168440600-168446400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
20	chr1:168440800-168443400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr1:168440800-168444200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr1:168442400-168447400	Enhancers	HepG2	liver
23	chr1:168442600-168444200	Enhancers	Fetal Intestine Large	intestine
24	chr1:168443000-168443200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr1:168443200-168443600	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
26	chr1:168443400-168444000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr1:168443400-168444000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr1:168443400-168444200	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr1:168443400-168444200	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr1:168443400-168444200	ZNF genes & repeats	Liver	Liver
31	chr1:168443400-168444200	ZNF genes & repeats	Spleen	Spleen
32	chr1:168443600-168444000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
33	chr1:168443600-168444200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr1:168443600-168445800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr1:168444000-168449800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr1:168444000-168450200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr1:168444000-168451400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr1:168444200-168444400	Weak transcription	Right Ventricle	heart
39	chr1:168444200-168444600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr1:168444200-168445000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr1:168444200-168445800	Weak transcription	Fetal Intestine Large	intestine
42	chr1:168444200-168446000	Weak transcription	Spleen	Spleen
43	chr1:168444200-168450400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr1:168444200-168450400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr1:168444200-168461000	Weak transcription	Liver	Liver
46	chr1:168444600-168445800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr1:168445000-168445200	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr1:168445000-168445600	Enhancers	NHEK	skin
49	chr1:168445000-168446000	Enhancers	HMEC	breast
50	chr1:168445200-168445800	Weak transcription	Cortex derived primary cultured neurospheres	brain

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