Variant report

Variant	nsv535172
Chromosome Location	chr1:153209833-153263691
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:797)
CpG islands
(count:733)
Chromatin interactive
region (count:23)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:797 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr1:153235181-153235634	GM12878	blood:	n/a	n/a
2	ATF3	chr1:153250419-153250603	K562	blood:	n/a	n/a
3	BACH1	chr1:153261175-153261426	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr1:153235286-153235585	GM12878	blood:	n/a	n/a
5	BATF	chr1:153226206-153226475	GM12878	blood:	n/a	n/a
6	BATF	chr1:153226175-153226483	GM12878	blood:	n/a	n/a
7	BATF	chr1:153250380-153250692	GM12878	blood:	n/a	n/a
8	BATF	chr1:153235249-153235686	GM12878	blood:	n/a	n/a
9	BCL11A	chr1:153235216-153235581	GM12878	blood:	n/a	n/a
10	BCL11A	chr1:153235180-153235674	GM12878	blood:	n/a	n/a
11	BHLHE40	chr1:153250409-153250701	GM12878	blood:	n/a	n/a
12	BHLHE40	chr1:153261334-153261370	GM12878	blood:	n/a	n/a
13	BHLHE40	chr1:153261225-153261367	K562	blood:	n/a	n/a
14	BHLHE40	chr1:153250390-153250662	K562	blood:	n/a	n/a
15	BRCA1	chr1:153250416-153250642	H1-hESC	embryonic stem cell:	n/a	n/a
16	CBX3	chr1:153250189-153250774	HCT-116	colon:	n/a	n/a
17	CEBPB	chr1:153250293-153250658	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr1:153250321-153250538	K562	blood:	n/a	n/a
19	CEBPB	chr1:153252705-153252766	K562	blood:	n/a	chr1:153252707-153252718
20	CEBPB	chr1:153211156-153211259	HepG2	liver:	n/a	n/a
21	CEBPB	chr1:153263021-153263086	IMR90	lung:	n/a	chr1:153263032-153263043
22	CEBPB	chr1:153210982-153211410	MCF-7	breast:	n/a	n/a
23	CEBPB	chr1:153250275-153250706	MCF-7	breast:	n/a	n/a
24	CEBPB	chr1:153211128-153211343	K562	blood:	n/a	n/a
25	CEBPB	chr1:153262946-153263099	HepG2	liver:	n/a	chr1:153263032-153263043
26	CEBPB	chr1:153252594-153252876	HepG2	liver:	n/a	chr1:153252707-153252718
27	CEBPB	chr1:153211174-153211269	Hela-S3	cervix:	n/a	n/a
28	CHD1	chr1:153234436-153234462	GM12878	blood:	n/a	n/a
29	CREB1	chr1:153235184-153235713	GM12878	blood:	n/a	n/a
30	CTCF	chr1:153250340-153250490	WI-38	lung:	n/a	n/a
31	CTCF	chr1:153250360-153250510	NHDF-neo	bronchial:	n/a	n/a
32	CTCF	chr1:153261168-153261485	GM19238	blood:	n/a	chr1:153261317-153261333 chr1:153261311-153261332 chr1:153261318-153261331 chr1:153261269-153261278 chr1:153261195-153261203 chr1:153261316-153261334
33	CTCF	chr1:153261240-153261390	RPTEC	kidney:	n/a	chr1:153261317-153261333 chr1:153261311-153261332 chr1:153261318-153261331 chr1:153261269-153261278 chr1:153261316-153261334
34	CTCF	chr1:153250460-153250610	NHEK	skin:	n/a	n/a
35	CTCF	chr1:153250454-153250655	Kidney_OC	kidney:	n/a	n/a
36	CTCF	chr1:153211109-153211266	GM19240	blood:	n/a	n/a
37	CTCF	chr1:153261119-153261506	K562	blood:	n/a	chr1:153261317-153261333 chr1:153261311-153261332 chr1:153261318-153261331 chr1:153261269-153261278 chr1:153261147-153261155 chr1:153261195-153261203 chr1:153261316-153261334
38	CTCF	chr1:153261160-153261310	RPTEC	kidney:	n/a	chr1:153261269-153261278 chr1:153261195-153261203
39	CTCF	chr1:153261220-153261370	HMEC	breast:	n/a	chr1:153261317-153261333 chr1:153261311-153261332 chr1:153261318-153261331 chr1:153261269-153261278 chr1:153261316-153261334
40	CTCF	chr1:153250429-153250615	SK-N-SH_RA	brain:	n/a	n/a
41	CTCF	chr1:153261165-153261477	GM12892	blood:	n/a	chr1:153261317-153261333 chr1:153261311-153261332 chr1:153261318-153261331 chr1:153261269-153261278 chr1:153261195-153261203 chr1:153261316-153261334
42	CTCF	chr1:153211140-153211290	HRE	kidney:	n/a	n/a
43	CTCF	chr1:153250500-153250650	GM12864	blood:	n/a	n/a
44	CTCF	chr1:153250460-153250610	SAEC	small airway:	n/a	n/a
45	CTCF	chr1:153250480-153250630	HEK293	kidney:	n/a	n/a
46	CTCF	chr1:153211020-153211387	GM12878	blood:	n/a	n/a
47	CTCF	chr1:153211100-153211250	GM12865	blood:	n/a	n/a
48	CTCF	chr1:153234760-153234910	GM12873	blood:	n/a	n/a
49	CTCF	chr1:153250520-153250670	HFF-Myc	foreskin:	n/a	n/a
50	CTCF	chr1:153261263-153261361	Kidney_OC	kidney:	n/a	chr1:153261317-153261333 chr1:153261311-153261332 chr1:153261318-153261331 chr1:153261269-153261278 chr1:153261316-153261334

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:153230907-153230957	U87	brain:	n/a
2	chr1:153230907-153230957	U87	brain:	n/a
3	chr1:153234387-153234437	SAEC	small airway:	n/a
4	chr1:153232348-153232398	LNCaP	prostate:	n/a
5	chr1:153234387-153234437	AG10803	skin:	n/a
6	chr1:153232060-153232110	AG04450	lung:	fetal
7	chr1:153230907-153230957	AG10803	skin:	n/a
8	chr1:153234037-153234087	Jurkat	blood:	n/a
9	chr1:153234387-153234437	HL-60	blood:	n/a
10	chr1:153232076-153232126	HPAEpiC	pulmonary alveolar:	n/a
11	chr1:153230941-153230991	Hepatocyte	liver:	n/a
12	chr1:153230941-153230991	GM12892	blood:	n/a
13	chr1:153234342-153234392	HCPEpiC	choroid plexus:	n/a
14	chr1:153232348-153232398	RPTEC	kidney:	n/a
15	chr1:153230907-153230957	AG04450	lung:	fetal
16	chr1:153233279-153233329	HIPEpiC	eye:	n/a
17	chr1:153234037-153234087	SAEC	small airway:	n/a
18	chr1:153234268-153234318	Hela-S3	cervix:	n/a
19	chr1:153233279-153233329	HEK293	kidney:	embryo
20	chr1:153234037-153234087	AG04449	skin:	fetal
21	chr1:153232460-153232510	HepG2	liver:	n/a
22	chr1:153230941-153230991	LNCaP	prostate:	n/a
23	chr1:153232348-153232398	NT2-D1	testis:	n/a
24	chr1:153232348-153232398	ProgFib	skin:	n/a
25	chr1:153234809-153234859	H1-hESC	embryonic stem cell:	embryo
26	chr1:153234342-153234392	HUVEC	blood vessel:	n/a
27	chr1:153230907-153230957	GM12891	blood:	n/a
28	chr1:153230941-153230991	HEEpiC	esophagus:	n/a
29	chr1:153230907-153230957	HRPEpiC	eye:	n/a
30	chr1:153234268-153234318	SAEC	small airway:	n/a
31	chr1:153234268-153234318	PFSK-1	brain:	n/a
32	chr1:153233279-153233329	HRPEpiC	eye:	n/a
33	chr1:153232060-153232110	HRPEpiC	eye:	n/a
34	chr1:153233279-153233329	BE2_C	brain:	n/a
35	chr1:153234387-153234437	AG04449	skin:	fetal
36	chr1:153232460-153232510	Caco-2	colon:	n/a
37	chr1:153234037-153234087	HEEpiC	esophagus:	n/a
38	chr1:153232348-153232398	NH-A	brain:	n/a
39	chr1:153232076-153232126	NHDF-neo	bronchial:	n/a
40	chr1:153230907-153230957	HNPCEpiC	eye:	n/a
41	chr1:153234387-153234437	HRPEpiC	eye:	n/a
42	chr1:153232348-153232398	NHDF-neo	bronchial:	n/a
43	chr1:153230941-153230991	RPTEC	kidney:	n/a
44	chr1:153234268-153234318	PrEC	prostate:	n/a
45	chr1:153232460-153232510	SK-N-MC	brain:	n/a
46	chr1:153233279-153233329	ECC-1	luminal epithelium:	n/a
47	chr1:153232348-153232398	T-47D	breast:	n/a
48	chr1:153234037-153234087	Caco-2	colon:	n/a
49	chr1:153232348-153232398	MCF10A-Er-Src	breast:	n/a
50	chr1:153234387-153234437	H1-hESC	embryonic stem cell:	embryo

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:153165121..153165850-chr1:153250100..153250641,2	MCF-7	breast:
2	chr1:153250021..153250689-chr3:65661545..65662381,2	MCF-7	breast:
3	chr1:153210336..153211688-chr1:153249859..153250680,4	MCF-7	breast:
4	chr1:153237506..153240487-chr1:153240538..153242898,2	MCF-7	breast:
5	chr1:153228030..153230897-chr1:153244661..153246633,2	K562	blood:
6	chr1:153253921..153255603-chr1:153263239..153265822,2	MCF-7	breast:
7	chr1:153234471..153235981-chr1:153239092..153241290,2	K562	blood:
8	chr1:153234471..153235981-chr1:153239092..153241290,2	K562	blood:
9	chr1:153210767..153211815-chr1:153250037..153251042,12	MCF-7	breast:
10	chr1:153213411..153215461-chr1:153315506..153317506,2	MCF-7	breast:
11	chr1:153211131..153211662-chr1:153377212..153377839,2	K562	blood:
12	chr1:153210767..153211815-chr1:153250037..153251042,12	MCF-7	breast:
13	chr1:153203220..153203749-chr1:153211972..153212774,2	MCF-7	breast:
14	chr1:153263271..153264922-chr1:153280009..153281672,2	MCF-7	breast:
15	chr1:153211248..153213332-chr1:153213671..153216662,2	MCF-7	breast:
16	chr1:153210770..153211595-chr1:153326032..153327205,3	MCF-7	breast:
17	chr1:153228030..153230897-chr1:153244661..153246633,2	K562	blood:
18	chr1:152842102..152843011-chr1:153260862..153261761,2	K562	blood:
19	chr1:153210019..153212643-chr20:45875612..45877137,2	MCF-7	breast:
20	chr1:153210336..153211688-chr1:153249859..153250680,4	MCF-7	breast:
21	chr1:153237506..153240487-chr1:153240538..153242898,2	MCF-7	breast:
22	chr1:153253921..153255603-chr1:153263239..153265822,2	MCF-7	breast:
23	chr1:153211248..153213332-chr1:153213671..153216662,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LOR-5	chr1:153250116-153250387	expReg_chr1_17210_+
2	lnc-LOR-4	chr1:153216878-153217186	NONHSAT006512
3	lnc-LOR-3	chr1:153247450-153247754	expReg_chr1_17194_+
4	lnc-LOR-1	chr1:153243431-153243816	expReg_chr1_17168_+
5	lnc-LOR-2	chr1:153246123-153246405	expReg_chr1_17185_+

No data

Variant related genes	Relation type
LOR	TF binding region
LOR	CpG island

Extended variants
information (count: 1659 )
Associated
traits (count: 131 )

Variant overlapped rSNPs/rCNVs (count:1659 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs115008440	chr1:153209882-153209883	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs149518941	chr1:153209895-153209896	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs542946142	chr1:153209919-153209920	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs562831135	chr1:153209931-153209932	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs116029963	chr1:153209948-153209949	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs545223293	chr1:153209955-153209956	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs200641665	chr1:153209970-153209971	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs565387145	chr1:153210003-153210004	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs374160640	chr1:153210028-153210029	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs74748604	chr1:153210142-153210143	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs76182474	chr1:153210160-153210161	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs1536823	chr1:153210182-153210183	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs74653448	chr1:153210188-153210189	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs550140595	chr1:153210208-153210209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs376320952	chr1:153210254-153210255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs182524208	chr1:153210297-153210298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs538831281	chr1:153210353-153210354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs202213597	chr1:153210423-153210424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs115651772	chr1:153210453-153210454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs565786220	chr1:153210508-153210509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs114134691	chr1:153210520-153210521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs554225065	chr1:153210547-153210548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs55736513	chr1:153210596-153210597	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs543009379	chr1:153210597-153210598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs116679362	chr1:153210600-153210601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs376445849	chr1:153210680-153210681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs187171398	chr1:153210729-153210730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs191228693	chr1:153210744-153210745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs12122588	chr1:153210760-153210761	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs4845342	chr1:153210808-153210809	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs541573446	chr1:153210812-153210813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs368222482	chr1:153210826-153210827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs376718568	chr1:153210827-153210828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs182609916	chr1:153210828-153210829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs187662541	chr1:153210839-153210840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs563610543	chr1:153210852-153210853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs111463169	chr1:153210886-153210887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs542755013	chr1:153210893-153210894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs4845531	chr1:153210929-153210930	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs193217091	chr1:153210989-153210990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs546854129	chr1:153211063-153211064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs547926292	chr1:153211156-153211157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs144028191	chr1:153211173-153211174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs542794084	chr1:153211181-153211182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs556648994	chr1:153211205-153211206	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs114363408	chr1:153211238-153211239	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs74136421	chr1:153211261-153211262	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs559188672	chr1:153211308-153211309	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs185035967	chr1:153211313-153211314	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs556980195	chr1:153211342-153211343	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:131)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	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
Systemic lupus erythematosus	21956041	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	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
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
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	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
Follicular lymphoma	18703704	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Gastrointestinal cancer	16790693	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Glioblastoma multiforme	21138945	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Breast cancer	21611746	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:447 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:153205200-153215600	Weak transcription	Spleen	Spleen
2	chr1:153209600-153210200	Enhancers	Stomach Mucosa	stomach
3	chr1:153210200-153215600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr1:153211200-153211400	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr1:153211400-153221200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr1:153214400-153217800	Weak transcription	Right Atrium	heart
7	chr1:153215000-153217800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr1:153215600-153215800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr1:153215600-153215800	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr1:153215600-153215800	Flanking Active TSS	Esophagus	oesophagus
11	chr1:153215600-153215800	Enhancers	Spleen	Spleen
12	chr1:153215800-153216000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr1:153215800-153216800	Weak transcription	Esophagus	oesophagus
14	chr1:153216000-153217000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr1:153216800-153217200	Enhancers	Esophagus	oesophagus
16	chr1:153217000-153217600	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr1:153217600-153222200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr1:153221000-153221200	Bivalent Enhancer	Left Ventricle	heart
19	chr1:153221000-153224200	Enhancers	Fetal Brain Male	brain
20	chr1:153221200-153223400	Enhancers	Breast Myoepithelial Primary Cells	Breast
21	chr1:153222200-153222600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr1:153222200-153223000	Enhancers	Brain Angular Gyrus	brain
23	chr1:153222800-153223000	Enhancers	Esophagus	oesophagus
24	chr1:153222800-153223400	Bivalent Enhancer	Adipose Nuclei	Adipose
25	chr1:153223000-153223400	Bivalent/Poised TSS	Fetal Kidney	kidney
26	chr1:153223000-153224000	Weak transcription	Esophagus	oesophagus
27	chr1:153223400-153223800	Enhancers	Adipose Nuclei	Adipose
28	chr1:153223400-153225800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
29	chr1:153223600-153225000	Enhancers	Primary neutrophils fromperipheralblood	blood
30	chr1:153224000-153224400	Enhancers	Esophagus	oesophagus
31	chr1:153224000-153224800	Enhancers	GM12878-XiMat	blood
32	chr1:153224200-153227800	Weak transcription	Fetal Brain Male	brain
33	chr1:153224400-153224600	Weak transcription	Esophagus	oesophagus
34	chr1:153224600-153225000	Enhancers	Esophagus	oesophagus
35	chr1:153224800-153225800	Weak transcription	GM12878-XiMat	blood
36	chr1:153225800-153226400	Enhancers	GM12878-XiMat	blood
37	chr1:153225800-153227200	Enhancers	Breast Myoepithelial Primary Cells	Breast
38	chr1:153227800-153228200	Enhancers	Fetal Brain Male	brain
39	chr1:153228200-153228400	Bivalent Enhancer	Fetal Brain Male	brain
40	chr1:153230600-153230800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
41	chr1:153231400-153231600	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr1:153232800-153233000	Enhancers	GM12878-XiMat	blood
43	chr1:153232800-153233200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
44	chr1:153232800-153233200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
45	chr1:153232800-153233400	Enhancers	Primary T killer memory cells from peripheral blood	blood
46	chr1:153232800-153233600	Bivalent Enhancer	Primary B cells from peripheral blood	blood
47	chr1:153232800-153234000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
48	chr1:153233000-153233200	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
49	chr1:153233000-153233200	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
50	chr1:153233000-153233200	Bivalent/Poised TSS	Primary B cells from cord blood	blood

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