Variant report

Variant	esv1819664
Chromosome Location	chr1:144502863-144522535
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:721)
CpG islands
(count:549)
Chromatin interactive
region (count:1)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:721 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr1:144507461-144507711	GM12878	blood:	n/a	n/a
2	BATF	chr1:144505988-144506367	GM12878	blood:	n/a	chr1:144506225-144506236
3	BATF	chr1:144518142-144518372	GM12878	blood:	n/a	n/a
4	BATF	chr1:144521730-144522322	GM12878	blood:	n/a	n/a
5	BATF	chr1:144514091-144514321	GM12878	blood:	n/a	n/a
6	BATF	chr1:144508099-144508353	GM12878	blood:	n/a	n/a
7	BATF	chr1:144509060-144509281	GM12878	blood:	n/a	n/a
8	BATF	chr1:144503041-144503309	GM12878	blood:	n/a	n/a
9	BATF	chr1:144513389-144513659	GM12878	blood:	n/a	n/a
10	BATF	chr1:144519521-144519990	GM12878	blood:	n/a	n/a
11	BATF	chr1:144519358-144521451	GM12878	blood:	n/a	n/a
12	BATF	chr1:144506111-144506279	GM12878	blood:	n/a	chr1:144506225-144506236
13	BATF	chr1:144509096-144509307	GM12878	blood:	n/a	n/a
14	BATF	chr1:144517018-144517384	GM12878	blood:	n/a	n/a
15	BATF	chr1:144518896-144519120	GM12878	blood:	n/a	n/a
16	BATF	chr1:144520625-144520932	GM12878	blood:	n/a	n/a
17	BATF	chr1:144521633-144522521	GM12878	blood:	n/a	n/a
18	BCL11A	chr1:144508971-144509318	GM12878	blood:	n/a	n/a
19	BCL11A	chr1:144511264-144511562	GM12878	blood:	n/a	n/a
20	BCL11A	chr1:144515026-144515216	GM12878	blood:	n/a	n/a
21	BCL11A	chr1:144519476-144521443	GM12878	blood:	n/a	chr1:144520101-144520110 chr1:144520329-144520342 chr1:144520377-144520386 chr1:144520691-144520704 chr1:144520378-144520391 chr1:144521379-144521388 chr1:144521327-144521340 chr1:144521320-144521333
22	BCL11A	chr1:144506123-144506377	GM12878	blood:	n/a	n/a
23	BCL11A	chr1:144516496-144516697	GM12878	blood:	n/a	n/a
24	BCL11A	chr1:144518215-144518501	GM12878	blood:	n/a	n/a
25	BCL11A	chr1:144521697-144522330	GM12878	blood:	n/a	chr1:144522062-144522071
26	BCL11A	chr1:144521627-144522519	GM12878	blood:	n/a	chr1:144522338-144522345 chr1:144522062-144522071
27	BCL11A	chr1:144503003-144503238	GM12878	blood:	n/a	n/a
28	BCL11A	chr1:144507164-144507443	GM12878	blood:	n/a	n/a
29	BCL11A	chr1:144518822-144521528	GM12878	blood:	n/a	chr1:144520101-144520110 chr1:144520329-144520342 chr1:144520377-144520386 chr1:144520691-144520704 chr1:144520378-144520391 chr1:144521379-144521388 chr1:144521327-144521340 chr1:144521320-144521333
30	BCL11A	chr1:144513343-144513579	GM12878	blood:	n/a	n/a
31	BCL3	chr1:144520027-144520189	GM12878	blood:	n/a	chr1:144520101-144520110
32	BHLHE40	chr1:144519960-144520144	GM12878	blood:	n/a	chr1:144520051-144520067
33	BHLHE40	chr1:144520208-144520496	HepG2	liver:	n/a	chr1:144520374-144520390 chr1:144520427-144520443
34	BHLHE40	chr1:144520861-144521057	GM12878	blood:	n/a	n/a
35	CEBPB	chr1:144520346-144520348	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr1:144520317-144520542	K562	blood:	n/a	n/a
37	CEBPB	chr1:144519394-144520093	GM12878	blood:	n/a	n/a
38	CEBPB	chr1:144520239-144520564	K562	blood:	n/a	n/a
39	CHD2	chr1:144520992-144520994	GM12878	blood:	n/a	n/a
40	CREB1	chr1:144520041-144520220	GM12878	blood:	n/a	n/a
41	CTCF	chr1:144520540-144520690	HEK293	kidney:	n/a	n/a
42	CTCF	chr1:144520500-144520650	SK-N-SH_RA	brain:	n/a	n/a
43	CTCF	chr1:144519887-144520174	K562	blood:	n/a	chr1:144520034-144520047 chr1:144520061-144520074
44	CTCF	chr1:144519969-144520096	Gliobla	brain:	n/a	chr1:144520034-144520047 chr1:144520061-144520074
45	CTCF	chr1:144521045-144521050	Gliobla	brain:	n/a	n/a
46	CTCF	chr1:144519983-144520129	GM10248	blood:	n/a	chr1:144520034-144520047 chr1:144520061-144520074
47	CTCF	chr1:144519969-144520008	A549	lung:	n/a	n/a
48	CTCF	chr1:144520422-144520474	LNCaP	prostate:	n/a	n/a
49	CTCF	chr1:144519810-144520300	K562	blood:	n/a	chr1:144520034-144520047 chr1:144520272-144520280 chr1:144520061-144520074
50	CTCF	chr1:144520520-144520670	GM12867	blood:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:144519573-144519623	CMK	blood:	n/a
2	chr1:144520201-144520251	CMK	blood:	n/a
3	chr1:144522237-144522287	A549	lung:	n/a
4	chr1:144522237-144522287	HPAEpiC	pulmonary alveolar:	n/a
5	chr1:144520991-144521041	IMR90	lung:	fetal
6	chr1:144513999-144514049	LNCaP	prostate:	n/a
7	chr1:144521462-144521512	SKMC	muscle:	n/a
8	chr1:144521081-144521131	Hepatocyte	liver:	n/a
9	chr1:144521228-144521278	SK-N-SH_RA	brain:	n/a
10	chr1:144521228-144521278	HEK293	kidney:	embryo
11	chr1:144522237-144522287	GM19239	blood:	n/a
12	chr1:144521228-144521278	BE2_C	brain:	n/a
13	chr1:144513999-144514049	HRE	kidney:	n/a
14	chr1:144519573-144519623	HEEpiC	esophagus:	n/a
15	chr1:144520156-144520206	Hela-S3	cervix:	n/a
16	chr1:144520991-144521041	ECC-1	luminal epithelium:	n/a
17	chr1:144520991-144521041	CMK	blood:	n/a
18	chr1:144520991-144521041	ovcar-3	ovarian:	n/a
19	chr1:144519573-144519623	HIPEpiC	eye:	n/a
20	chr1:144522237-144522287	HAEpiC	amniotic membrane:	n/a
21	chr1:144521228-144521278	PrEC	prostate:	n/a
22	chr1:144522237-144522287	MCF10A-Er-Src	breast:	n/a
23	chr1:144521081-144521131	Jurkat	blood:	n/a
24	chr1:144521462-144521512	HEK293	kidney:	embryo
25	chr1:144521081-144521131	AG09309	skin:	n/a
26	chr1:144521462-144521512	HPAEpiC	pulmonary alveolar:	n/a
27	chr1:144520156-144520206	HCM	heart:	n/a
28	chr1:144521228-144521278	Hela-S3	cervix:	n/a
29	chr1:144520201-144520251	A549	lung:	n/a
30	chr1:144513999-144514049	SK-N-MC	brain:	n/a
31	chr1:144522237-144522287	LNCaP	prostate:	n/a
32	chr1:144521081-144521131	GM19239	blood:	n/a
33	chr1:144521228-144521278	HMEC	breast:	n/a
34	chr1:144520201-144520251	Hela-S3	cervix:	n/a
35	chr1:144521081-144521131	HCPEpiC	choroid plexus:	n/a
36	chr1:144520991-144521041	MCF-7	breast:	n/a
37	chr1:144520201-144520251	AG09309	skin:	n/a
38	chr1:144521081-144521131	H1-hESC	embryonic stem cell:	embryo
39	chr1:144520991-144521041	K562	blood:	n/a
40	chr1:144521228-144521278	Hepatocyte	liver:	n/a
41	chr1:144520156-144520206	HUVEC	blood vessel:	n/a
42	chr1:144520156-144520206	AG09319	gingival:	n/a
43	chr1:144521081-144521131	ovcar-3	ovarian:	n/a
44	chr1:144521462-144521512	LNCaP	prostate:	n/a
45	chr1:144513999-144514049	HMEC	breast:	n/a
46	chr1:144520201-144520251	SKMC	muscle:	n/a
47	chr1:144521081-144521131	NB4	blood:	n/a
48	chr1:144520156-144520206	MCF-7	breast:	n/a
49	chr1:144522237-144522287	AG04449	skin:	fetal
50	chr1:144521228-144521278	HAEpiC	amniotic membrane:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:144519367..144521165-chr1:144533246..144535069,2	K562	blood:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PPIAL4B-2	chr1:144520774-144520871	ENSG00000236943.1
2	lnc-PPIAL4B-2	chr1:144521884-144521969	NONHSAT005803
3	lnc-PPIAL4B-2	chr1:144520774-144520871	NONHSAT005803
4	lnc-PPIAL4B-2	chr1:144506277-144506436	ENSG00000236943.1
5	lnc-PPIAL4B-2	chr1:144520774-144521002	ENSG00000236943.1
6	lnc-PPIAL4B-2	chr1:144516478-144516503	ENSG00000236943.1
7	lnc-PPIAL4B-2	chr1:144521884-144521970	ENSG00000236943.1
8	lnc-PPIAL4B-2	chr1:144520774-144520841	ENSG00000236943.1
9	lnc-PPIAL4B-2	chr1:144520774-144520983	ENSG00000236943.1
10	lnc-PPIAL4B-2	chr1:144506277-144506436	ENSG00000236943.1
11	lnc-PPIAL4B-2	chr1:144514874-144519720	NONHSAT005809
12	lnc-PPIAL4B-2	chr1:144519813-144519867	ENSG00000236943.1
13	lnc-PPIAL4B-2	chr1:144505804-144505925	ENSG00000236943.1
14	lnc-PPIAL4B-2	chr1:144506091-144506436	ENSG00000236943.1
15	lnc-PPIAL4B-2	chr1:144516419-144516729	ENSG00000236943.1
16	lnc-PPIAL4B-2	chr1:144521639-144522054	NONHSAT005811
17	lnc-PPIAL4B-2	chr1:144520774-144520919	ENSG00000236943.1
18	lnc-PPIAL4B-2	chr1:144520774-144520993	ENSG00000236943.1

No data

Variant related genes	Relation type
ENSG00000236943	TF binding region
ENSG00000236943	CpG island
ENSG00000201699	chromatin interactions

Extended variants
information (count: 156 )
Associated
traits (count: 167 )

Variant overlapped rSNPs/rCNVs (count:156 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs61802348	chr1:144506182-144506183	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs61802349	chr1:144506283-144506284	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs557084	chr1:144506348-144506349	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs144944932	chr1:144507306-144507307	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs61802353	chr1:144507407-144507408	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs11485972	chr1:144507590-144507591	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs77147333	chr1:144515204-144515205	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs587727225	chr1:144516403-144516404	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs199972360	chr1:144517580-144517581	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs200788367	chr1:144517715-144517716	Enhancers Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
11	rs2935839	chr1:144517819-144517820	Enhancers Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
12	rs201573042	chr1:144517841-144517842	Enhancers Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
13	rs61802358	chr1:144517858-144517859	Enhancers Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
14	rs587620305	chr1:144517864-144517865	Enhancers Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
15	rs508978	chr1:144517899-144517900	Enhancers Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
16	rs200265663	chr1:144517918-144517919	Enhancers Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
17	rs201923620	chr1:144517986-144517987	Enhancers Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
18	rs200790003	chr1:144518067-144518068	Enhancers Weak transcription Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
19	rs510827	chr1:144518097-144518098	Enhancers Weak transcription Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
20	rs659144	chr1:144518117-144518118	Enhancers Weak transcription Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
21	rs512528	chr1:144518276-144518277	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
22	rs375755963	chr1:144518292-144518293	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
23	rs61802963	chr1:144518328-144518329	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
24	rs61802964	chr1:144518354-144518355	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
25	rs201885043	chr1:144518365-144518366	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
26	rs587693319	chr1:144518522-144518523	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
27	rs4247991	chr1:144518608-144518609	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
28	rs200584358	chr1:144518629-144518630	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
29	rs376314654	chr1:144518816-144518817	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
30	rs587757088	chr1:144519146-144519147	Weak transcription Enhancers Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
31	rs587647486	chr1:144519170-144519171	Weak transcription Enhancers Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
32	rs151085852	chr1:144519342-144519343	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
33	rs371556864	chr1:144519343-144519344	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
34	rs587690241	chr1:144519347-144519348	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
35	rs368186949	chr1:144519552-144519553	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
36	rs372065410	chr1:144519607-144519608	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
37	rs145521130	chr1:144519609-144519610	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
38	rs202138850	chr1:144519615-144519616	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
39	rs587746165	chr1:144519627-144519628	Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
40	rs587623238	chr1:144519636-144519637	Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
41	rs200461970	chr1:144519650-144519651	Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
42	rs587656140	chr1:144519651-144519652	Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
43	rs587711975	chr1:144519802-144519803	Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs200486718	chr1:144519860-144519861	Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
45	rs377362148	chr1:144519899-144519900	Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs587594508	chr1:144519922-144519923	Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs376573006	chr1:144520009-144520010	Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs587667680	chr1:144520017-144520018	Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs145633456	chr1:144520021-144520022	Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs371879743	chr1:144520050-144520051	Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:167)

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
small cell lung cancer	20016488	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
Breast cancer	21611746	CNVD
Retinoblastoma	19183342	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22499536	CNVD
Schizophrenia	18923514	CNVD
Neuroblastoma	21124317	CNVD
Autism	20970697	CNVD
Bipolar disorder	19114987	CNVD
Epilepsy	20970697	CNVD
Schizophrenia	22118685	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	21956041	CNVD
Schizophrenia	20970697	CNVD
Addison''s disease	21851588	CNVD
Heart disease	22199024	CNVD
Mental retardation	19951919	CNVD
Ovarian cancer	20844748	CNVD
Schizophrenia	21399695	CNVD
Prostate cancer	17217626	CNVD
Congenital heart defect	22199024	CNVD
TAR Syndrome	17847015	CNVD
Thrombocytopenia-absent radius syndrome	17236129	CNVD
Autism	18784092	CNVD
Congenital abnormalities	18784092	CNVD
Mental retardation	18784092	CNVD
Schizophrenia	19855392	CNVD
Ovarian cancer	22174824	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
Autism	19521722	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	19521646	CNVD
Neuroblastoma	19536264	CNVD
Epilepsy	20923578	CNVD
Mental retardation	17124404	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18668039	CNVD
Schizophrenia	19443537	CNVD
Schizophrenia	19571808	CNVD
Velocardiofacial syndrome	19329560	CNVD
Autism	19955444	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Colorectal cancer	20459617	CNVD
Osteosarcoma	19286668	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
Breast cancer	17142309	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	18703704	CNVD
Lung adenocarcinoma	17982442	CNVD
Breast cancer	21509527	CNVD
Williams Syndrome	20824207	CNVD
Tetralogy of Fallot	22912587	CNVD
Autism	18522746	CNVD
Schizophrenia	23813976	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Schizophrenia	19197363	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Schizophrenia	20967226	CNVD
Breast cancer	22522925	CNVD
Lung adenocarcinoma	21935476	CNVD
idiopathic generalized epilepsy	19843651	CNVD
Schizophrenia	19843651	CNVD
Cancer	17440070	CNVD

Chromatin state (count:237 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:144507200-144507600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
2	chr1:144507200-144507600	Enhancers	Fetal Intestine Small	intestine
3	chr1:144507400-144507600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
4	chr1:144517600-144518200	Active TSS	Primary T helper naive cells from peripheral blood	blood
5	chr1:144517600-144518200	Enhancers	Primary T helper cells fromperipheralblood	blood
6	chr1:144517600-144518400	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr1:144517600-144518400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
8	chr1:144517600-144518600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
9	chr1:144517800-144518000	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr1:144517800-144518200	Active TSS	Primary T killer memory cells from peripheral blood	blood
11	chr1:144517800-144518400	Active TSS	Pancreatic Islets	Pancreatic Islet
12	chr1:144517800-144518600	Enhancers	Primary T helper cells PMA-I stimulated	--
13	chr1:144518000-144519200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
14	chr1:144518200-144518400	Enhancers	H1 Cell Line	embryonic stem cell
15	chr1:144518200-144518400	Enhancers	H9 Cell Line	embryonic stem cell
16	chr1:144518200-144518400	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr1:144518200-144518400	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr1:144518200-144518400	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr1:144518200-144518400	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr1:144518200-144518400	Enhancers	Primary neutrophils fromperipheralblood	blood
21	chr1:144518200-144518400	Enhancers	Primary B cells from cord blood	blood
22	chr1:144518200-144518400	Enhancers	Primary B cells from peripheral blood	blood
23	chr1:144518200-144518400	Enhancers	Primary T cells from cord blood	blood
24	chr1:144518200-144518400	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
25	chr1:144518200-144518400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
26	chr1:144518200-144518400	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
27	chr1:144518200-144518400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
28	chr1:144518200-144518400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
29	chr1:144518200-144518400	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
30	chr1:144518200-144518400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr1:144518200-144518400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr1:144518200-144518400	Enhancers	Liver	Liver
33	chr1:144518200-144518400	Enhancers	Fetal Intestine Large	intestine
34	chr1:144518200-144518400	Enhancers	Fetal Lung	lung
35	chr1:144518200-144518400	Enhancers	NHEK	skin
36	chr1:144518400-144519000	Weak transcription	HUES64 Cell Line	embryonic stem cell
37	chr1:144518400-144519000	Weak transcription	Primary neutrophils fromperipheralblood	blood
38	chr1:144518400-144519000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
39	chr1:144518400-144519000	Weak transcription	Primary T helper cells fromperipheralblood	blood
40	chr1:144518400-144519000	Weak transcription	Fetal Intestine Large	intestine
41	chr1:144518400-144519200	Weak transcription	HUES48 Cell Line	embryonic stem cell
42	chr1:144518400-144519200	Weak transcription	Primary T cells from cord blood	blood
43	chr1:144518400-144519200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
44	chr1:144518400-144519200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
45	chr1:144518400-144519200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
46	chr1:144518400-144519200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
47	chr1:144518400-144519200	Weak transcription	Pancreatic Islets	Pancreatic Islet
48	chr1:144518400-144519400	Weak transcription	Liver	Liver
49	chr1:144518400-144519400	Weak transcription	Fetal Lung	lung
50	chr1:144518600-144519000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood

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