Variant report

Variant	esv6733
Chromosome Location	chr1:153285308-153321521
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:461)
CpG islands
(count:245)
Chromatin interactive
region (count:29)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:461 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:153316224-153316564	K562	blood:	n/a	n/a
2	ATF1	chr1:153316188-153316707	K562	blood:	n/a	n/a
3	ATF2	chr1:153317901-153318732	GM12878	blood:	n/a	n/a
4	BACH1	chr1:153316310-153316560	K562	blood:	n/a	n/a
5	BCL11A	chr1:153318035-153318602	GM12878	blood:	n/a	chr1:153318156-153318165
6	BCL3	chr1:153316226-153316742	K562	blood:	n/a	n/a
7	BHLHE40	chr1:153289548-153289686	HepG2	liver:	n/a	n/a
8	BHLHE40	chr1:153320525-153320834	K562	blood:	n/a	n/a
9	BHLHE40	chr1:153316678-153316844	GM12878	blood:	n/a	n/a
10	BHLHE40	chr1:153314673-153314942	K562	blood:	n/a	n/a
11	BHLHE40	chr1:153316328-153316400	GM12878	blood:	n/a	n/a
12	BHLHE40	chr1:153312255-153312620	GM12878	blood:	n/a	n/a
13	BHLHE40	chr1:153316026-153317463	K562	blood:	n/a	n/a
14	BHLHE40	chr1:153317883-153319176	GM12878	blood:	n/a	n/a
15	CBX3	chr1:153316185-153316747	K562	blood:	n/a	n/a
16	CBX3	chr1:153316070-153316771	K562	blood:	n/a	n/a
17	CCNT2	chr1:153316163-153317014	K562	blood:	n/a	n/a
18	CCNT2	chr1:153314497-153315106	K562	blood:	n/a	n/a
19	CEBPB	chr1:153321231-153321560	Hela-S3	cervix:	n/a	chr1:153321396-153321409 chr1:153321396-153321407
20	CEBPB	chr1:153321130-153321716	MCF-7	breast:	n/a	chr1:153321396-153321409 chr1:153321396-153321407
21	CEBPB	chr1:153321257-153321544	H1-hESC	embryonic stem cell:	n/a	chr1:153321396-153321409 chr1:153321396-153321407
22	CEBPB	chr1:153285291-153285772	MCF-7	breast:	n/a	chr1:153285508-153285519
23	CEBPB	chr1:153317263-153317548	K562	blood:	n/a	n/a
24	CEBPB	chr1:153285373-153285590	HepG2	liver:	n/a	chr1:153285508-153285519
25	CEBPB	chr1:153321313-153321446	IMR90	lung:	n/a	chr1:153321396-153321409 chr1:153321396-153321407
26	CEBPB	chr1:153285467-153285614	H1-hESC	embryonic stem cell:	n/a	chr1:153285508-153285519
27	CEBPB	chr1:153316118-153316685	K562	blood:	n/a	n/a
28	CEBPB	chr1:153321311-153321511	A549	lung:	n/a	chr1:153321396-153321409 chr1:153321396-153321407
29	CEBPB	chr1:153321129-153321667	MCF-7	breast:	n/a	chr1:153321396-153321409 chr1:153321396-153321407
30	CEBPB	chr1:153321233-153321581	K562	blood:	n/a	chr1:153321396-153321409 chr1:153321396-153321407
31	CEBPB	chr1:153285361-153285558	K562	blood:	n/a	chr1:153285508-153285519
32	CEBPB	chr1:153316214-153316725	K562	blood:	n/a	n/a
33	CEBPB	chr1:153321241-153321519	HepG2	liver:	n/a	chr1:153321396-153321409 chr1:153321396-153321407
34	CEBPD	chr1:153316105-153316836	K562	blood:	n/a	n/a
35	CEBPD	chr1:153315982-153316816	K562	blood:	n/a	n/a
36	CHD1	chr1:153316652-153317290	GM12878	blood:	n/a	n/a
37	CHD1	chr1:153312474-153312507	GM12878	blood:	n/a	n/a
38	CHD1	chr1:153318612-153319211	GM12878	blood:	n/a	n/a
39	CHD1	chr1:153315416-153315539	GM12878	blood:	n/a	n/a
40	CHD2	chr1:153316470-153316471	K562	blood:	n/a	n/a
41	CHD2	chr1:153317913-153319371	GM12878	blood:	n/a	n/a
42	CHD2	chr1:153316313-153316508	GM12878	blood:	n/a	n/a
43	CHD2	chr1:153316860-153317439	GM12878	blood:	n/a	n/a
44	CTCF	chr1:153285220-153285370	GM12872	blood:	n/a	chr1:153285232-153285245
45	CTCF	chr1:153321080-153321230	MCF-7	breast:	n/a	n/a
46	CTCF	chr1:153316477-153316581	K562	blood:	n/a	n/a
47	CTCF	chr1:153321060-153321210	Caco-2	colon:	n/a	n/a
48	CTCF	chr1:153285240-153285390	HCT-116	colon:	n/a	n/a
49	CTCF	chr1:153285161-153285372	NHEK	skin:	n/a	chr1:153285232-153285245
50	CTCF	chr1:153321040-153321190	Caco-2	colon:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:153312501-153312551	CMK	blood:	n/a
2	chr1:153312501-153312551	CMK	blood:	n/a
3	chr1:153320414-153320464	HIPEpiC	eye:	n/a
4	chr1:153312501-153312551	U87	brain:	n/a
5	chr1:153321198-153321248	HCM	heart:	n/a
6	chr1:153320414-153320464	AG10803	skin:	n/a
7	chr1:153321198-153321248	GM12878	blood:	n/a
8	chr1:153321198-153321248	AG04450	lung:	fetal
9	chr1:153321421-153321471	SK-N-MC	brain:	n/a
10	chr1:153320414-153320464	CMK	blood:	n/a
11	chr1:153321421-153321471	ovcar-3	ovarian:	n/a
12	chr1:153321421-153321471	NHBE	bronchial:	n/a
13	chr1:153312501-153312551	RPTEC	kidney:	n/a
14	chr1:153320414-153320464	HNPCEpiC	eye:	n/a
15	chr1:153321198-153321248	SAEC	small airway:	n/a
16	chr1:153321421-153321471	GM19239	blood:	n/a
17	chr1:153321421-153321471	AG04450	lung:	fetal
18	chr1:153312501-153312551	GM12891	blood:	n/a
19	chr1:153321421-153321471	Hepatocyte	liver:	n/a
20	chr1:153321421-153321471	HRE	kidney:	n/a
21	chr1:153320414-153320464	AG09309	skin:	n/a
22	chr1:153312501-153312551	ovcar-3	ovarian:	n/a
23	chr1:153312501-153312551	AG04449	skin:	fetal
24	chr1:153312501-153312551	NHBE	bronchial:	n/a
25	chr1:153321198-153321248	T-47D	breast:	n/a
26	chr1:153312501-153312551	HRE	kidney:	n/a
27	chr1:153312501-153312551	BE2_C	brain:	n/a
28	chr1:153312501-153312551	HCT-116	colon:	n/a
29	chr1:153320414-153320464	GM12892	blood:	n/a
30	chr1:153321198-153321248	HEK293	kidney:	embryo
31	chr1:153320414-153320464	U87	brain:	n/a
32	chr1:153320414-153320464	HRE	kidney:	n/a
33	chr1:153312501-153312551	SAEC	small airway:	n/a
34	chr1:153312501-153312551	ProgFib	skin:	n/a
35	chr1:153312501-153312551	A549	lung:	n/a
36	chr1:153321198-153321248	HAEpiC	amniotic membrane:	n/a
37	chr1:153312501-153312551	MCF10A-Er-Src	breast:	n/a
38	chr1:153320414-153320464	HCM	heart:	n/a
39	chr1:153320414-153320464	RPTEC	kidney:	n/a
40	chr1:153320414-153320464	HAEpiC	amniotic membrane:	n/a
41	chr1:153320414-153320464	HEEpiC	esophagus:	n/a
42	chr1:153312501-153312551	SK-N-SH	brain:	n/a
43	chr1:153321198-153321248	NH-A	brain:	n/a
44	chr1:153321198-153321248	HCPEpiC	choroid plexus:	n/a
45	chr1:153321421-153321471	PFSK-1	brain:	n/a
46	chr1:153321421-153321471	Caco-2	colon:	n/a
47	chr1:153312501-153312551	Hepatocyte	liver:	n/a
48	chr1:153320414-153320464	PFSK-1	brain:	n/a
49	chr1:153321421-153321471	K562	blood:	n/a
50	chr1:153320414-153320464	GM12878	blood:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:153295502..153298458-chr1:153310854..153312535,3	MCF-7	breast:
2	chr1:153294084..153298144-chr1:153301195..153303853,4	MCF-7	breast:
3	chr1:153307876..153311044-chr1:153313486..153317217,5	K562	blood:
4	chr1:153320974..153341807-chr1:153456098..153486349,81	MCF-7	breast:
5	chr1:153312042..153314259-chr1:153317727..153320410,2	MCF-7	breast:
6	chr1:153318291..153319996-chr1:153322460..153325006,2	K562	blood:
7	chr1:153284760..153285743-chr1:153325777..153326381,2	MCF-7	breast:
8	chr1:153315494..153319256-chr1:153320325..153322468,4	MCF-7	breast:
9	chr1:153318218..153321043-chr1:153328281..153331716,3	MCF-7	breast:
10	chr1:153308815..153311044-chr1:153314101..153317217,4	K562	blood:
11	chr1:153297965..153300595-chr1:153301047..153303956,2	MCF-7	breast:
12	chr1:153294084..153298144-chr1:153301195..153303853,4	MCF-7	breast:
13	chr1:153285307..153287264-chr1:153311060..153313468,2	MCF-7	breast:
14	chr1:153297965..153300595-chr1:153301047..153303956,2	MCF-7	breast:
15	chr1:153274688..153277090-chr1:153283483..153285851,2	K562	blood:
16	chr1:153310086..153312333-chr1:153317510..153319218,3	K562	blood:
17	chr1:153308815..153311044-chr1:153314101..153317217,4	K562	blood:
18	chr1:153314988..153319996-chr1:153321870..153325921,5	K562	blood:
19	chr1:153310086..153312333-chr1:153317510..153319218,3	K562	blood:
20	chr1:153285307..153287264-chr1:153311060..153313468,2	MCF-7	breast:
21	chr1:153307876..153311044-chr1:153313486..153317217,5	K562	blood:
22	chr1:153312042..153314259-chr1:153317727..153320410,2	MCF-7	breast:
23	chr1:153316827..153319773-chr1:153324804..153327111,2	MCF-7	breast:
24	chr1:153294490..153296567-chr1:153297370..153299941,2	MCF-7	breast:
25	chr1:153295502..153298458-chr1:153310854..153312535,3	MCF-7	breast:
26	chr1:153305058..153307996-chr1:153320640..153322441,2	MCF-7	breast:
27	chr1:153213411..153215461-chr1:153315506..153317506,2	MCF-7	breast:
28	chr1:153294490..153296567-chr1:153297370..153299941,2	MCF-7	breast:
29	chr1:153295251..153295999-chr5:12761269..12762010,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PGLYRP4-1	chr1:153284290-153303044	predAs_engstrom06_CR598625_1
2	lnc-S100A12-3	chr1:153317501-153317846	NONHSAT006515
3	lnc-S100A12-3	chr1:153318578-153318667	NONHSAT006515
4	lnc-S100A12-3	chr1:153320360-153320454	NONHSAT006515

No data

Variant related genes	Relation type
PGLYRP3	TF binding region
RNU6-160P	TF binding region
PGLYRP4	TF binding region
PGLYRP3	CpG island
RNU6-160P	CpG island
PGLYRP4	CpG island
ENSG00000263841	chromatin interactions
ENSG00000163218	chromatin interactions
ENSG00000163220	chromatin interactions

Extended variants
information (count: 1504 )
Associated
traits (count: 125 )

Variant overlapped rSNPs/rCNVs (count:1504 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs78131848	chr1:153285312-153285313	Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
2	rs377405564	chr1:153285320-153285321	Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
3	rs72706901	chr1:153285330-153285331	Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
4	rs376195550	chr1:153285345-153285346	Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
5	rs572205386	chr1:153285346-153285347	Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
6	rs541267840	chr1:153285403-153285404	Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
7	rs554784303	chr1:153285408-153285409	Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
8	rs574620161	chr1:153285423-153285424	Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
9	rs527346316	chr1:153285428-153285429	Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs181415867	chr1:153285463-153285464	Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
11	rs373655077	chr1:153285464-153285465	Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
12	rs563347595	chr1:153285469-153285470	Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
13	rs150569811	chr1:153285481-153285482	Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
14	rs564259063	chr1:153285560-153285561	Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
15	rs143712953	chr1:153285574-153285575	Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
16	rs567629596	chr1:153285578-153285579	Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
17	rs565614553	chr1:153285579-153285580	Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
18	rs536904768	chr1:153285612-153285613	Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
19	rs547610214	chr1:153285616-153285617	Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
20	rs567502190	chr1:153285649-153285650	Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
21	rs116174259	chr1:153285691-153285692	Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
22	rs146324622	chr1:153285765-153285766	Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
23	rs553389827	chr1:153285783-153285784	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
24	rs2987762	chr1:153285786-153285787	Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs3006489	chr1:153285787-153285788	Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs558670449	chr1:153285853-153285854	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
27	rs565994599	chr1:153285854-153285855	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
28	rs534900166	chr1:153285859-153285860	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
29	rs554870275	chr1:153285875-153285876	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
30	rs574708205	chr1:153285969-153285970	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
31	rs537199777	chr1:153286007-153286008	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
32	rs2987763	chr1:153286034-153286035	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs377450927	chr1:153286052-153286053	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
34	rs576857251	chr1:153286144-153286145	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
35	rs545832774	chr1:153286150-153286151	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
36	rs139269512	chr1:153286196-153286197	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
37	rs149979947	chr1:153286209-153286210	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
38	rs2987764	chr1:153286218-153286219	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs548934249	chr1:153286223-153286224	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
40	rs561215591	chr1:153286236-153286237	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
41	rs181903702	chr1:153286241-153286242	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
42	rs549921396	chr1:153286270-153286271	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
43	rs550467180	chr1:153286302-153286303	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
44	rs148701058	chr1:153286366-153286367	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
45	rs186309842	chr1:153286462-153286463	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
46	rs552576143	chr1:153286472-153286473	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
47	rs148902957	chr1:153286473-153286474	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
48	rs534989780	chr1:153286521-153286522	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
49	rs548508567	chr1:153286641-153286642	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
50	rs568322929	chr1:153286644-153286645	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:125)

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
Glioblastoma multiforme	21510904	CNVD
Breast cancer	22522925	CNVD
Follicular lymphoma	20505157	CNVD
Neuroblastoma	18923191	CNVD
Lung adenocarcinoma	21935476	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:212 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:153285000-153285400	Enhancers	Esophagus	oesophagus
2	chr1:153285000-153285400	Enhancers	HMEC	breast
3	chr1:153285000-153285800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr1:153285000-153286000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr1:153285200-153285400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr1:153292200-153292800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr1:153303000-153303200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr1:153303600-153305200	ZNF genes & repeats	GM12878-XiMat	blood
9	chr1:153305200-153308400	Weak transcription	GM12878-XiMat	blood
10	chr1:153308400-153309800	Enhancers	GM12878-XiMat	blood
11	chr1:153308400-153310800	Enhancers	Fetal Brain Male	brain
12	chr1:153309200-153309400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
13	chr1:153309400-153309800	Enhancers	Fetal Brain Female	brain
14	chr1:153309800-153311200	Weak transcription	GM12878-XiMat	blood
15	chr1:153310400-153313200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr1:153311200-153311400	Enhancers	GM12878-XiMat	blood
17	chr1:153311400-153311800	Weak transcription	GM12878-XiMat	blood
18	chr1:153311600-153313000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
19	chr1:153311600-153313000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
20	chr1:153311800-153312200	Enhancers	Primary T cells from cord blood	blood
21	chr1:153311800-153312600	Enhancers	GM12878-XiMat	blood
22	chr1:153311800-153313000	Enhancers	Primary hematopoietic stem cells	blood
23	chr1:153311800-153313000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
24	chr1:153311800-153313000	Enhancers	Primary T helper cells fromperipheralblood	blood
25	chr1:153311800-153313000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr1:153311800-153313200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
27	chr1:153311800-153313200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr1:153312000-153313200	Enhancers	Fetal Thymus	thymus
29	chr1:153312200-153312600	Flanking Active TSS	Primary T cells from cord blood	blood
30	chr1:153312200-153312800	Enhancers	Primary T cells fromperipheralblood	blood
31	chr1:153312200-153312800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
32	chr1:153312200-153313000	Enhancers	Primary hematopoietic stem cells short term culture	blood
33	chr1:153312200-153313000	Enhancers	Primary T killer memory cells from peripheral blood	blood
34	chr1:153312200-153313200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
35	chr1:153312200-153313200	Enhancers	Primary T helper cells PMA-I stimulated	--
36	chr1:153312200-153313800	Enhancers	Primary T helper naive cells from peripheral blood	blood
37	chr1:153312400-153312600	Enhancers	Primary neutrophils fromperipheralblood	blood
38	chr1:153312400-153312600	Enhancers	Esophagus	oesophagus
39	chr1:153312400-153312800	Enhancers	NHEK	skin
40	chr1:153312400-153313000	Enhancers	HMEC	breast
41	chr1:153312400-153313200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
42	chr1:153312400-153313200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
43	chr1:153312600-153313000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
44	chr1:153312600-153313000	Flanking Active TSS	GM12878-XiMat	blood
45	chr1:153312600-153315600	Weak transcription	Esophagus	oesophagus
46	chr1:153312600-153316000	Enhancers	Primary T cells from cord blood	blood
47	chr1:153312800-153313200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
48	chr1:153312800-153315200	Weak transcription	NHEK	skin
49	chr1:153312800-153315600	Weak transcription	Primary neutrophils fromperipheralblood	blood
50	chr1:153313000-153313400	Weak transcription	Primary hematopoietic stem cells	blood

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