Variant report

Variant	nsv999251
Chromosome Location	chr1:10276263-10318163
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:248)
CpG islands
(count:122)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 1)
miRNA target
sites (count:1)

(count:248 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:10313857-10314010	HepG2	liver:	n/a	chr1:10313897-10313913
2	ARID3A	chr1:10288507-10288965	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:10290872-10291007	K562	blood:	n/a	n/a
4	ATF1	chr1:10288922-10289087	K562	blood:	n/a	n/a
5	BATF	chr1:10298398-10298570	GM12878	blood:	n/a	chr1:10298491-10298502
6	BHLHE40	chr1:10296582-10296647	GM12878	blood:	n/a	n/a
7	BHLHE40	chr1:10278126-10278526	GM12878	blood:	n/a	n/a
8	BHLHE40	chr1:10297230-10297583	GM12878	blood:	n/a	n/a
9	BHLHE40	chr1:10276157-10276385	GM12878	blood:	n/a	n/a
10	CBX3	chr1:10290696-10291317	HCT-116	colon:	n/a	n/a
11	CBX3	chr1:10290715-10291307	HCT-116	colon:	n/a	n/a
12	CEBPB	chr1:10312565-10312752	IMR90	lung:	n/a	n/a
13	CEBPB	chr1:10290779-10291089	IMR90	lung:	n/a	n/a
14	CEBPB	chr1:10318059-10318259	HepG2	liver:	n/a	chr1:10318131-10318142
15	CEBPB	chr1:10290681-10291321	HCT-116	colon:	n/a	n/a
16	CEBPB	chr1:10276333-10276418	K562	blood:	n/a	n/a
17	CEBPB	chr1:10290689-10291309	HCT-116	colon:	n/a	n/a
18	CEBPB	chr1:10313856-10314265	IMR90	lung:	n/a	n/a
19	CEBPB	chr1:10311824-10312111	IMR90	lung:	n/a	n/a
20	CEBPB	chr1:10285709-10285965	IMR90	lung:	n/a	n/a
21	CEBPD	chr1:10280304-10280665	K562	blood:	n/a	n/a
22	CREB1	chr1:10311723-10312128	GM12878	blood:	n/a	n/a
23	CREB1	chr1:10311716-10312073	GM12878	blood:	n/a	n/a
24	CTCF	chr1:10303385-10303458	MCF-7	breast:	n/a	n/a
25	CTCF	chr1:10278280-10278430	AG10803	skin:	n/a	chr1:10278309-10278319
26	CTCF	chr1:10278319-10278349	GM10266	blood:	n/a	n/a
27	CTCF	chr1:10278220-10278370	HCPEpiC	choroid plexus:	n/a	chr1:10278309-10278319
28	CTCF	chr1:10278240-10278390	AG10803	skin:	n/a	chr1:10278309-10278319
29	CTCF	chr1:10310840-10310990	HRE	kidney:	n/a	n/a
30	CTCF	chr1:10278320-10278470	HMF	breast:	n/a	n/a
31	CUX1	chr1:10276315-10276323	GM12878	blood:	n/a	n/a
32	CUX1	chr1:10296555-10297651	GM12878	blood:	n/a	n/a
33	E2F4	chr1:10311835-10312094	MCF10A-Er-Src	breast:	n/a	n/a
34	EBF1	chr1:10297155-10297568	GM12878	blood:	n/a	n/a
35	EBF1	chr1:10276666-10276710	GM12878	blood:	n/a	n/a
36	EBF1	chr1:10278095-10278431	GM12878	blood:	n/a	n/a
37	ELK1	chr1:10296614-10296619	GM12878	blood:	n/a	n/a
38	EP300	chr1:10313938-10314146	K562	blood:	n/a	n/a
39	EP300	chr1:10288525-10288935	HepG2	liver:	n/a	n/a
40	EP300	chr1:10296516-10296653	GM12878	blood:	n/a	n/a
41	EP300	chr1:10276165-10276460	GM12878	blood:	n/a	n/a
42	EP300	chr1:10278231-10278444	GM12878	blood:	n/a	n/a
43	EP300	chr1:10276307-10276394	K562	blood:	n/a	n/a
44	EP300	chr1:10276039-10276664	GM12878	blood:	n/a	n/a
45	EP300	chr1:10296609-10297659	GM12878	blood:	n/a	chr1:10296757-10296771 chr1:10297343-10297357 chr1:10297444-10297453
46	EP300	chr1:10276182-10276467	GM12878	blood:	n/a	n/a
47	EP300	chr1:10297136-10297604	GM12878	blood:	n/a	chr1:10297343-10297357 chr1:10297444-10297453
48	FAM48A	chr1:10303564-10303693	GM12878	blood:	n/a	n/a
49	FOS	chr1:10290757-10291179	MCF10A-Er-Src	breast:	n/a	chr1:10290999-10291010 chr1:10290944-10290952 chr1:10290942-10290954 chr1:10290942-10290953 chr1:10290943-10290954
50	FOS	chr1:10311440-10312176	MCF10A-Er-Src	breast:	n/a	chr1:10311986-10311994 chr1:10311984-10311996

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:10277983-10278033	SAEC	small airway:	n/a
2	chr1:10314029-10314079	ovcar-3	ovarian:	n/a
3	chr1:10314029-10314079	BE2_C	brain:	n/a
4	chr1:10314029-10314079	IMR90	lung:	fetal
5	chr1:10277983-10278033	AG10803	skin:	n/a
6	chr1:10314029-10314079	PANC-1	pancreas:	n/a
7	chr1:10314029-10314079	HRE	kidney:	n/a
8	chr1:10277983-10278033	Jurkat	blood:	n/a
9	chr1:10314029-10314079	HepG2	liver:	n/a
10	chr1:10277983-10278033	HIPEpiC	eye:	n/a
11	chr1:10277983-10278033	GM12891	blood:	n/a
12	chr1:10277983-10278033	NHBE	bronchial:	n/a
13	chr1:10277983-10278033	HCF	heart:	n/a
14	chr1:10277983-10278033	HNPCEpiC	eye:	n/a
15	chr1:10277983-10278033	AG09309	skin:	n/a
16	chr1:10314029-10314079	ECC-1	luminal epithelium:	n/a
17	chr1:10277983-10278033	Caco-2	colon:	n/a
18	chr1:10277983-10278033	HRPEpiC	eye:	n/a
19	chr1:10277983-10278033	PANC-1	pancreas:	n/a
20	chr1:10277983-10278033	HRE	kidney:	n/a
21	chr1:10314029-10314079	HEK293	kidney:	embryo
22	chr1:10277983-10278033	HepG2	liver:	n/a
23	chr1:10314029-10314079	AG04450	lung:	fetal
24	chr1:10314029-10314079	HCM	heart:	n/a
25	chr1:10314029-10314079	NT2-D1	testis:	n/a
26	chr1:10314029-10314079	GM12878	blood:	n/a
27	chr1:10314029-10314079	AG09309	skin:	n/a
28	chr1:10314029-10314079	GM06990	blood:	n/a
29	chr1:10314029-10314079	PrEC	prostate:	n/a
30	chr1:10314029-10314079	A549	lung:	n/a
31	chr1:10314029-10314079	Jurkat	blood:	n/a
32	chr1:10277983-10278033	BE2_C	brain:	n/a
33	chr1:10277983-10278033	HEK293	kidney:	embryo
34	chr1:10314029-10314079	HRCEpiC	kidney:	n/a
35	chr1:10277983-10278033	HCT-116	colon:	n/a
36	chr1:10314029-10314079	HAEpiC	amniotic membrane:	n/a
37	chr1:10277983-10278033	CMK	blood:	n/a
38	chr1:10277983-10278033	HL-60	blood:	n/a
39	chr1:10314029-10314079	HEEpiC	esophagus:	n/a
40	chr1:10314029-10314079	PFSK-1	brain:	n/a
41	chr1:10277983-10278033	IMR90	lung:	fetal
42	chr1:10314029-10314079	HRPEpiC	eye:	n/a
43	chr1:10314029-10314079	HCT-116	colon:	n/a
44	chr1:10277983-10278033	PrEC	prostate:	n/a
45	chr1:10314029-10314079	RPTEC	kidney:	n/a
46	chr1:10277983-10278033	SK-N-SH_RA	brain:	n/a
47	chr1:10277983-10278033	Hela-S3	cervix:	n/a
48	chr1:10277983-10278033	SK-N-SH	brain:	n/a
49	chr1:10277983-10278033	T-47D	breast:	n/a
50	chr1:10277983-10278033	Hepatocyte	liver:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr1:10282059..10284111-chr1:10292781..10294603,2	K562	blood:
2	chr1:10270579..10272996-chr1:10274200..10277824,5	K562	blood:
3	chr1:10282059..10284111-chr1:10292781..10294603,2	K562	blood:
4	chr1:10278325..10279914-chr1:10289402..10290960,2	K562	blood:
5	chr1:10272332..10273838-chr1:10278117..10280308,2	K562	blood:
6	chr1:10276579..10278410-chr1:10297316..10299169,2	K562	blood:
7	chr1:10313731..10315777-chr1:10317109..10319777,2	K562	blood:
8	chr1:10270307..10271947-chr1:10273665..10276309,2	MCF-7	breast:
9	chr1:10288684..10290909-chr1:10294452..10296809,3	K562	blood:
10	chr1:10298304..10299209-chr3:122134645..122135581,2	NB4	blood:
11	chr1:10312327..10314244-chr1:10342279..10344001,2	MCF-7	breast:
12	chr1:10288561..10290129-chr1:10291840..10294041,2	K562	blood:
13	chr1:10284668..10286801-chr1:10289342..10292166,2	K562	blood:
14	chr1:9901779..9904041-chr1:10302410..10304191,2	K562	blood:
15	chr1:10313731..10315777-chr1:10317109..10319777,2	K562	blood:
16	chr1:10269360..10271630-chr1:10278085..10280674,3	MCF-7	breast:
17	chr1:10268925..10271698-chr1:10297795..10299727,2	MCF-7	breast:
18	chr1:10276579..10278410-chr1:10297316..10299169,2	K562	blood:

No data

miRNA name	Chromosome Location	mirBase accession
hsa-miR-1273d	chr1:10287785-10287809	MIMAT0015090

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	KIF1B	hsa-miR-9-5p	chr1:10316308-10316331

Variant related genes	Relation type
MIR1273D	TF binding region
KIF1B	TF binding region
MIR1273D	CpG island
KIF1B	CpG island
ENSG00000272758	chromatin interactions
ENSG00000054523	chromatin interactions
ENSG00000196981	chromatin interactions

Extended variants
information (count: 1644 )
Associated
traits (count: 119 )

Variant overlapped rSNPs/rCNVs (count:1644 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs570056121	chr1:10276372-10276373	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs78517415	chr1:10276373-10276374	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs191652521	chr1:10276386-10276387	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs577163450	chr1:10276412-10276413	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs541279915	chr1:10276421-10276422	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs148878913	chr1:10276446-10276447	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs574898609	chr1:10276484-10276485	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs537665781	chr1:10276605-10276606	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs541929125	chr1:10276616-10276617	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs563265929	chr1:10276618-10276619	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs549566080	chr1:10276627-10276628	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs376502595	chr1:10276631-10276632	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs72864193	chr1:10276643-10276644	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs146466724	chr1:10276669-10276670	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs528401558	chr1:10276697-10276698	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs546876540	chr1:10276699-10276700	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs568277983	chr1:10276714-10276715	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs386628383	chr1:10276718-10276719	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs375168735	chr1:10276719-10276720	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs112090408	chr1:10276720-10276721	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs537549274	chr1:10276753-10276754	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs367667728	chr1:10276760-10276761	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs141506314	chr1:10276774-10276775	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs570469918	chr1:10276781-10276782	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs534998705	chr1:10276827-10276828	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs553221272	chr1:10276845-10276846	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs11800418	chr1:10276915-10276916	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs535706595	chr1:10276931-10276932	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs12032050	chr1:10276953-10276954	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs377682430	chr1:10277014-10277015	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs139941533	chr1:10277026-10277027	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs70998362	chr1:10277049-10277050	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs71643084	chr1:10277056-10277057	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs372438550	chr1:10277069-10277070	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs557523857	chr1:10277087-10277088	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs375450885	chr1:10277107-10277108	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs183853740	chr1:10277177-10277178	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs188176444	chr1:10277180-10277181	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs538758766	chr1:10277207-10277208	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs559159392	chr1:10277256-10277257	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs191345483	chr1:10277275-10277276	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs556755607	chr1:10277307-10277308	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs11121531	chr1:10277357-10277358	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs201126438	chr1:10277401-10277402	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs199943449	chr1:10277402-10277403	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs201031225	chr1:10277403-10277404	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs201831859	chr1:10277404-10277405	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs72638981	chr1:10277405-10277406	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs550547414	chr1:10277410-10277411	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs185829815	chr1:10277436-10277437	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:119)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Follicular lymphoma	18703704	CNVD
Lung cancer	22429812	CNVD
Epilepsy	22118685	CNVD
Schizophrenia	22118685	CNVD
Ovarian cancer	21720365	CNVD
Developmental delay	19490664	CNVD
Ewing''s sarcoma	21437220	CNVD
Prader-willi syndrome	18797701	CNVD
periventricular nodular heterotopia	20648244	CNVD
1p36 deletion syndrome	22283845	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
Neuroblastoma	18923524	CNVD
Retinoblastoma	22278416	CNVD
Mental retardation	20152051	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Astrocytoma	17934521	CNVD
Glioblastoma	20031968	CNVD
Acute myeloid leukemia	18000384	CNVD
Glioblastoma multiforme	16951158	CNVD
Neuroblastoma	18574593	CNVD
Glioblastoma multiforme	17369134	CNVD
Autism	18414403	CNVD
Breast cancer	17001317	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Myoepithelioma	18604193	CNVD
Wilms tumour	19047088	CNVD
Breast cancer	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Metanephric adenoma	20802469	CNVD
Soft tissue tumor	16732325	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Basal cell lymphoma	21115979	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic myeloid leukemia	21384125	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Neuroblastoma	18923191	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	20406844	CNVD
Glioblastoma multiforme	21138945	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ovarian neoplasms	16753589	CNVD
Neuroblastoma	19287153	CNVD
Hepatocellular carcinoma	18929564	CNVD
Melanoma	17363583	CNVD
renal disease	17924346	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Uveal melanoma	20484589	CNVD
Multiple myeloma	16616336	CNVD
Glioblastoma multiforme	22286061	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	20164919	CNVD
Autism	20808228	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1333 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:10272200-10276400	Weak transcription	Primary B cells from peripheral blood	blood
2	chr1:10272200-10276400	Weak transcription	Primary hematopoietic stem cells	blood
3	chr1:10272200-10276600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr1:10272200-10276600	Weak transcription	Spleen	Spleen
5	chr1:10272200-10277600	Weak transcription	Esophagus	oesophagus
6	chr1:10272200-10278000	Weak transcription	Colonic Mucosa	Colon
7	chr1:10272200-10278200	Weak transcription	Placenta	Placenta
8	chr1:10272400-10276400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr1:10272600-10277600	Weak transcription	Monocytes-CD14+_RO01746	blood
10	chr1:10272600-10277800	Weak transcription	Rectal Mucosa Donor 29	rectum
11	chr1:10272600-10277800	Weak transcription	Rectal Mucosa Donor 31	rectum
12	chr1:10272600-10284000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
13	chr1:10272600-10284000	Weak transcription	Fetal Intestine Small	intestine
14	chr1:10272600-10368200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr1:10272800-10276600	Weak transcription	Lung	lung
16	chr1:10272800-10277600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr1:10272800-10284000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr1:10272800-10284400	Weak transcription	Gastric	stomach
19	chr1:10272800-10290000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr1:10272800-10296600	Weak transcription	Placenta Amnion	Placenta Amnion
21	chr1:10273600-10277800	Weak transcription	Pancreatic Islets	Pancreatic Islet
22	chr1:10273600-10278200	Weak transcription	Fetal Intestine Large	intestine
23	chr1:10273800-10276600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr1:10273800-10276600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr1:10274000-10276400	Weak transcription	HSMMtube	muscle
26	chr1:10274000-10277800	Weak transcription	Fetal Kidney	kidney
27	chr1:10274000-10282400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr1:10274000-10285200	Weak transcription	HUES64 Cell Line	embryonic stem cell
29	chr1:10274200-10276400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr1:10274200-10276600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr1:10274200-10277000	Enhancers	Brain Germinal Matrix	brain
32	chr1:10274200-10277600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr1:10274200-10277800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr1:10274200-10277800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr1:10274200-10278200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr1:10274200-10284600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
37	chr1:10274400-10276400	Weak transcription	NHLF	lung
38	chr1:10274400-10276600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr1:10274400-10278000	Weak transcription	Fetal Stomach	stomach
40	chr1:10274600-10281200	Weak transcription	Fetal Muscle Trunk	muscle
41	chr1:10275000-10276400	Weak transcription	Fetal Muscle Leg	muscle
42	chr1:10275400-10277400	Enhancers	Cortex derived primary cultured neurospheres	brain
43	chr1:10275400-10278600	Enhancers	Psoas Muscle	Psoas
44	chr1:10275600-10276400	Enhancers	Skeletal Muscle Female	skeletal muscle
45	chr1:10275600-10276800	Enhancers	Primary T cells fromperipheralblood	blood
46	chr1:10275600-10276800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
47	chr1:10275600-10276800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
48	chr1:10275600-10276800	Enhancers	Primary T helper cells PMA-I stimulated	--
49	chr1:10275600-10277000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
50	chr1:10275600-10277000	Enhancers	Fetal Brain Female	brain

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