Variant report

Variant	nsv498699
Chromosome Location	chr1:192970436-192993624
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:192976723-192977711	HepG2	liver:	n/a	n/a
2	BATF	chr1:192973296-192973619	GM12878	blood:	n/a	chr1:192973439-192973450
3	BCL3	chr1:192976889-192977423	A549	lung:	n/a	n/a
4	BCL3	chr1:192978340-192978899	A549	lung:	n/a	n/a
5	BHLHE40	chr1:192976176-192976217	K562	blood:	n/a	n/a
6	CBX3	chr1:192988503-192988967	HCT-116	colon:	n/a	n/a
7	CCNT2	chr1:192980322-192980539	K562	blood:	n/a	n/a
8	CEBPB	chr1:192980568-192980846	Hela-S3	cervix:	n/a	chr1:192980715-192980728 chr1:192980717-192980726 chr1:192980717-192980726 chr1:192980715-192980728 chr1:192980715-192980726 chr1:192980717-192980728 chr1:192980717-192980726 chr1:192980717-192980726
9	CEBPB	chr1:192980540-192980898	K562	blood:	n/a	chr1:192980715-192980728 chr1:192980717-192980726 chr1:192980717-192980726 chr1:192980715-192980728 chr1:192980715-192980726 chr1:192980717-192980728 chr1:192980717-192980726 chr1:192980717-192980726
10	CEBPB	chr1:192980594-192980864	IMR90	lung:	n/a	chr1:192980715-192980728 chr1:192980717-192980726 chr1:192980717-192980726 chr1:192980715-192980728 chr1:192980715-192980726 chr1:192980717-192980728 chr1:192980717-192980726 chr1:192980717-192980726
11	CEBPB	chr1:192982217-192982528	IMR90	lung:	n/a	n/a
12	CEBPB	chr1:192976910-192977353	HepG2	liver:	n/a	n/a
13	CEBPB	chr1:192980548-192980815	A549	lung:	n/a	chr1:192980715-192980728 chr1:192980717-192980726 chr1:192980717-192980726 chr1:192980715-192980728 chr1:192980715-192980726 chr1:192980717-192980728 chr1:192980717-192980726 chr1:192980717-192980726
14	CEBPB	chr1:192980618-192980834	HepG2	liver:	n/a	chr1:192980715-192980728 chr1:192980717-192980726 chr1:192980717-192980726 chr1:192980715-192980728 chr1:192980715-192980726 chr1:192980717-192980728 chr1:192980717-192980726 chr1:192980717-192980726
15	CEBPZ	chr1:192977513-192977736	HepG2	liver:	n/a	n/a
16	CTCF	chr1:192988571-192988904	T-47D	breast:	n/a	chr1:192988762-192988780 chr1:192988757-192988778
17	CTCF	chr1:192988648-192988885	GM12878	blood:	n/a	chr1:192988762-192988780 chr1:192988757-192988778
18	CTCF	chr1:192988693-192988830	MCF-7	breast:	n/a	chr1:192988762-192988780 chr1:192988757-192988778
19	CTCF	chr1:192988610-192988840	T-47D	breast:	n/a	chr1:192988762-192988780 chr1:192988757-192988778
20	CTCF	chr1:192988640-192988790	GM12874	blood:	n/a	chr1:192988762-192988780 chr1:192988757-192988778
21	CTCF	chr1:192988680-192988865	LNCaP	prostate:	n/a	chr1:192988762-192988780 chr1:192988757-192988778
22	CTCF	chr1:192988640-192988790	AG09309	skin:	n/a	chr1:192988762-192988780 chr1:192988757-192988778
23	CTCF	chr1:192988629-192988909	Spleen_OC	spleen:	n/a	chr1:192988762-192988780 chr1:192988757-192988778
24	CTCF	chr1:192988720-192988870	HepG2	liver:	n/a	chr1:192988762-192988780 chr1:192988757-192988778
25	CTCF	chr1:192988660-192988810	HVMF	connective:	n/a	chr1:192988762-192988780 chr1:192988757-192988778
26	CTCF	chr1:192988659-192988862	GM10248	blood:	n/a	chr1:192988762-192988780 chr1:192988757-192988778
27	CTCF	chr1:192988640-192988790	Hela-S3	cervix:	n/a	chr1:192988762-192988780 chr1:192988757-192988778
28	CTCF	chr1:192988611-192988926	K562	blood:	n/a	chr1:192988762-192988780 chr1:192988757-192988778
29	CTCF	chr1:192988631-192988850	H1-hESC	embryonic stem cell:	n/a	chr1:192988762-192988780 chr1:192988757-192988778
30	CTCF	chr1:192988680-192988830	AG10803	skin:	n/a	chr1:192988762-192988780 chr1:192988757-192988778
31	CTCF	chr1:192988680-192988830	HPAF	blood vessel:	n/a	chr1:192988762-192988780 chr1:192988757-192988778
32	CTCF	chr1:192988640-192988790	HBMEC	blood vessel:	n/a	chr1:192988762-192988780 chr1:192988757-192988778
33	CTCF	chr1:192988682-192988897	Lung_OC	lung:	n/a	chr1:192988762-192988780 chr1:192988757-192988778
34	CTCF	chr1:192988640-192988790	Caco-2	colon:	n/a	chr1:192988762-192988780 chr1:192988757-192988778
35	CTCF	chr1:192988720-192988870	GM12866	blood:	n/a	chr1:192988762-192988780 chr1:192988757-192988778
36	CTCF	chr1:192988479-192989027	MCF-7	breast:	n/a	chr1:192988762-192988780 chr1:192988757-192988778
37	CTCF	chr1:192988680-192988830	HMF	breast:	n/a	chr1:192988762-192988780 chr1:192988757-192988778
38	CTCF	chr1:192988700-192988850	MCF-7	breast:	n/a	chr1:192988762-192988780 chr1:192988757-192988778
39	CTCF	chr1:192988640-192988790	HCT-116	colon:	n/a	chr1:192988762-192988780 chr1:192988757-192988778
40	CTCF	chr1:192988700-192988850	AoAF	blood vessel:	n/a	chr1:192988762-192988780 chr1:192988757-192988778
41	CTCF	chr1:192993369-192993375	GM10248	blood:	n/a	n/a
42	CTCF	chr1:192988522-192989046	HCT-116	colon:	n/a	chr1:192988762-192988780 chr1:192988757-192988778
43	CTCF	chr1:192988262-192989077	SK-N-SH	brain:	n/a	chr1:192988762-192988780 chr1:192988757-192988778
44	CTCF	chr1:192988632-192988913	HUVEC	blood vessel:	n/a	chr1:192988762-192988780 chr1:192988757-192988778
45	CTCF	chr1:192988572-192988868	A549	lung:	n/a	chr1:192988762-192988780 chr1:192988757-192988778
46	CTCF	chr1:192988591-192988922	A549	lung:	n/a	chr1:192988762-192988780 chr1:192988757-192988778
47	CTCF	chr1:192988620-192988770	RPTEC	kidney:	n/a	n/a
48	CTCF	chr1:192988660-192988810	GM12864	blood:	n/a	chr1:192988762-192988780 chr1:192988757-192988778
49	CTCF	chr1:192975796-192975839	GM13976	blood:	n/a	n/a
50	CTCF	chr1:192988612-192988818	SK-N-SH_RA	brain:	n/a	chr1:192988762-192988780 chr1:192988757-192988778

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:192983012-192983062	AG09309	skin:	n/a
2	chr1:192983012-192983062	Jurkat	blood:	n/a
3	chr1:192983012-192983062	Hela-S3	cervix:	n/a
4	chr1:192983012-192983062	ovcar-3	ovarian:	n/a
5	chr1:192983012-192983062	NT2-D1	testis:	n/a
6	chr1:192983012-192983062	HCPEpiC	choroid plexus:	n/a
7	chr1:192983012-192983062	HRCEpiC	kidney:	n/a
8	chr1:192983012-192983062	SAEC	small airway:	n/a
9	chr1:192983012-192983062	GM06990	blood:	n/a
10	chr1:192983012-192983062	GM19239	blood:	n/a
11	chr1:192983012-192983062	PrEC	prostate:	n/a
12	chr1:192983012-192983062	NHDF-neo	bronchial:	n/a
13	chr1:192983012-192983062	HAEpiC	amniotic membrane:	n/a
14	chr1:192983012-192983062	NHBE	bronchial:	n/a
15	chr1:192983012-192983062	IMR90	lung:	fetal
16	chr1:192983012-192983062	K562	blood:	n/a
17	chr1:192983012-192983062	NB4	blood:	n/a
18	chr1:192983012-192983062	T-47D	breast:	n/a
19	chr1:192983012-192983062	SK-N-SH_RA	brain:	n/a
20	chr1:192983012-192983062	PANC-1	pancreas:	n/a
21	chr1:192983012-192983062	AG04450	lung:	fetal
22	chr1:192983012-192983062	AG04449	skin:	fetal
23	chr1:192983012-192983062	HMEC	breast:	n/a
24	chr1:192983012-192983062	HEK293	kidney:	embryo
25	chr1:192983012-192983062	HCT-116	colon:	n/a
26	chr1:192983012-192983062	HEEpiC	esophagus:	n/a
27	chr1:192983012-192983062	HL-60	blood:	n/a
28	chr1:192983012-192983062	U87	brain:	n/a
29	chr1:192983012-192983062	MCF-7	breast:	n/a
30	chr1:192983012-192983062	AG10803	skin:	n/a
31	chr1:192983012-192983062	GM12892	blood:	n/a
32	chr1:192983012-192983062	NH-A	brain:	n/a
33	chr1:192983012-192983062	MCF10A-Er-Src	breast:	n/a
34	chr1:192983012-192983062	BE2_C	brain:	n/a
35	chr1:192983012-192983062	HNPCEpiC	eye:	n/a
36	chr1:192983012-192983062	HCF	heart:	n/a
37	chr1:192983012-192983062	A549	lung:	n/a
38	chr1:192983012-192983062	SKMC	muscle:	n/a
39	chr1:192983012-192983062	RPTEC	kidney:	n/a
40	chr1:192983012-192983062	HepG2	liver:	n/a
41	chr1:192983012-192983062	HPAEpiC	pulmonary alveolar:	n/a
42	chr1:192983012-192983062	CMK	blood:	n/a
43	chr1:192983012-192983062	GM12878	blood:	n/a
44	chr1:192983012-192983062	Caco-2	colon:	n/a
45	chr1:192983012-192983062	GM12891	blood:	n/a
46	chr1:192983012-192983062	LNCaP	prostate:	n/a
47	chr1:192983012-192983062	HIPEpiC	eye:	n/a
48	chr1:192983012-192983062	Hepatocyte	liver:	n/a
49	chr1:192983012-192983062	H1-hESC	embryonic stem cell:	embryo
50	chr1:192983012-192983062	HCM	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:192964363..192967314-chr1:192975848..192978969,3	K562	blood:
2	chr1:192978102..192980139-chr1:193100169..193103053,2	K562	blood:
3	chr1:192957649..192960395-chr1:192982012..192983675,2	K562	blood:
4	chr1:192973548..192977447-chr1:192979869..192983384,3	K562	blood:
5	chr1:192971893..192973529-chr1:192975096..192977591,2	K562	blood:
6	chr1:192984947..192986543-chr1:193027186..193029315,2	K562	blood:
7	chr1:192980684..192984723-chr1:192984841..192989093,4	K562	blood:
8	chr1:192446513..192447432-chr1:192988667..192989486,2	K562	blood:
9	chr1:192774616..192775596-chr1:192988271..192989252,4	K562	blood:
10	chr1:192973548..192977447-chr1:192979869..192983384,3	K562	blood:
11	chr1:192774668..192775652-chr1:192988368..192989269,6	MCF-7	breast:
12	chr1:192442920..192443850-chr1:192988643..192989239,2	K562	blood:
13	chr1:192970631..192973618-chr1:193027189..193029600,2	K562	blood:
14	chr1:192775702..192778041-chr1:192986871..192988604,2	MCF-7	breast:
15	chr1:192971893..192973529-chr1:192975096..192977591,2	K562	blood:
16	chr1:192976057..192978615-chr1:193027631..193029509,2	MCF-7	breast:
17	chr1:192980684..192984723-chr1:192984841..192989093,4	K562	blood:
18	chr1:192979947..192982887-chr1:192983438..192986734,3	K562	blood:
19	chr1:192979947..192982887-chr1:192983438..192986734,3	K562	blood:
20	chr1:192976396..192978239-chr1:192979297..192981493,2	MCF-7	breast:
21	chr1:192981169..192983545-chr1:192999201..193001195,2	K562	blood:
22	chr1:192992147..192995725-chr1:192998536..193000592,4	K562	blood:
23	chr1:192773819..192775227-chr1:192988234..192989224,6	MCF-7	breast:
24	chr1:192762496..192765465-chr1:192982382..192985012,2	K562	blood:
25	chr1:192976396..192978239-chr1:192979297..192981493,2	MCF-7	breast:
26	chr1:192446612..192447642-chr1:192988286..192989297,3	MCF-7	breast:

Variant related genes	Relation type
UCHL5	TF binding region
UCHL5	CpG island
ENSG00000116750	chromatin interactions
ENSG00000116747	chromatin interactions

Extended variants
information (count: 679 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:679 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs137969042	chr1:192970456-192970457	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs531869656	chr1:192970465-192970466	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs568614608	chr1:192970466-192970467	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs534492748	chr1:192970500-192970501	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs547850413	chr1:192970501-192970502	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs570843153	chr1:192970517-192970518	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs75795020	chr1:192970571-192970572	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs139693968	chr1:192970584-192970585	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs367772063	chr1:192970587-192970588	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs556638012	chr1:192970590-192970591	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs12740200	chr1:192970612-192970613	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs149123075	chr1:192970613-192970614	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs200032539	chr1:192970618-192970619	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs191828833	chr1:192970627-192970628	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs184133209	chr1:192970653-192970654	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs147137257	chr1:192970657-192970658	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs572057660	chr1:192970702-192970703	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs540919952	chr1:192970748-192970749	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs575397704	chr1:192970845-192970846	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs563774863	chr1:192970853-192970854	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs189455550	chr1:192970861-192970862	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs543022801	chr1:192970872-192970873	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs563412796	chr1:192970873-192970874	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs528933708	chr1:192970939-192970940	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs181066990	chr1:192970954-192970955	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs187345915	chr1:192970976-192970977	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs144419891	chr1:192971032-192971033	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs548085006	chr1:192971146-192971147	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs370858313	chr1:192971148-192971149	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs190518707	chr1:192971152-192971153	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs144902314	chr1:192971156-192971157	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs147544996	chr1:192971211-192971212	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs148589480	chr1:192971239-192971240	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs535577174	chr1:192971326-192971327	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs555184315	chr1:192971329-192971330	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs9427571	chr1:192971406-192971407	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs532353849	chr1:192971514-192971515	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs4658079	chr1:192971539-192971540	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs145167778	chr1:192971553-192971554	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs151090526	chr1:192971580-192971581	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs181458147	chr1:192971775-192971776	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs185956583	chr1:192971806-192971807	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs533376200	chr1:192971838-192971839	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs547125547	chr1:192971839-192971840	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs56022114	chr1:192971899-192971900	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs140969007	chr1:192971963-192971964	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs562296018	chr1:192971980-192971981	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs143740618	chr1:192972019-192972020	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs79662891	chr1:192972028-192972029	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs529026055	chr1:192972051-192972052	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	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
Glioblastoma multiforme	21080181	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
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	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
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	20688739	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21611746	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	17393978	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	19010865	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Trisomy 5 syndrome	21098271	CNVD
Glioblastoma multiforme	22286061	CNVD
Urothelial carcinoma	21177765	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Mental retardation	21062444	CNVD
Liver carcinoma	19366792	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:415 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:192938000-192972800	Weak transcription	Psoas Muscle	Psoas
2	chr1:192953600-192982400	Weak transcription	HSMMtube	muscle
3	chr1:192954200-192991200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
4	chr1:192954800-192978800	Weak transcription	Right Ventricle	heart
5	chr1:192955800-192972400	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr1:192955800-192990600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
7	chr1:192956200-192972000	Weak transcription	Brain Anterior Caudate	brain
8	chr1:192956200-192988400	Weak transcription	Brain Hippocampus Middle	brain
9	chr1:192961200-192983600	Weak transcription	Hela-S3	cervix
10	chr1:192961400-192976000	Weak transcription	HepG2	liver
11	chr1:192961800-192976200	Weak transcription	Rectal Mucosa Donor 31	rectum
12	chr1:192962600-192986400	Weak transcription	Placenta Amnion	Placenta Amnion
13	chr1:192963000-192982000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr1:192963600-192983000	Weak transcription	Primary T helper cells fromperipheralblood	blood
15	chr1:192963800-192972000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
16	chr1:192963800-192972000	Weak transcription	Adipose Nuclei	Adipose
17	chr1:192963800-192972600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr1:192963800-192973200	Weak transcription	Duodenum Smooth Muscle	Duodenum
19	chr1:192963800-192974800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr1:192963800-192981400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr1:192963800-192981600	Weak transcription	NHLF	lung
22	chr1:192963800-192982000	Weak transcription	Muscle Satellite Cultured Cells	--
23	chr1:192963800-192982200	Weak transcription	Aorta	Aorta
24	chr1:192963800-192983000	Weak transcription	NH-A	brain
25	chr1:192963800-192990000	Weak transcription	HMEC	breast
26	chr1:192963800-192994400	Weak transcription	Primary hematopoietic stem cells	blood
27	chr1:192963800-192996200	Weak transcription	Fetal Lung	lung
28	chr1:192963800-193012400	Weak transcription	NHEK	skin
29	chr1:192963800-193019600	Weak transcription	Ovary	ovary
30	chr1:192964000-192971400	Weak transcription	Liver	Liver
31	chr1:192964000-192972600	Weak transcription	Fetal Muscle Trunk	muscle
32	chr1:192964000-192973400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
33	chr1:192964000-192975000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
34	chr1:192964000-192977200	Weak transcription	Cortex derived primary cultured neurospheres	brain
35	chr1:192964000-192981000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr1:192964000-192981800	Weak transcription	HSMM	muscle
37	chr1:192964000-192983000	Weak transcription	Fetal Thymus	thymus
38	chr1:192964000-192984600	Weak transcription	Primary B cells from cord blood	blood
39	chr1:192964000-192990400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
40	chr1:192964000-192994400	Weak transcription	Left Ventricle	heart
41	chr1:192965000-192990800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr1:192966200-192971000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr1:192966200-192994200	Weak transcription	Primary T cells from cord blood	blood
44	chr1:192966400-192970800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr1:192966400-192976800	Weak transcription	A549	lung
46	chr1:192966400-192985200	Weak transcription	Primary T cells fromperipheralblood	blood
47	chr1:192967200-192970800	Weak transcription	Sigmoid Colon	Sigmoid Colon
48	chr1:192967200-192983600	Weak transcription	HUVEC	blood vessel
49	chr1:192967600-192982800	Weak transcription	Skeletal Muscle Female	skeletal muscle
50	chr1:192967600-192993000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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