Variant report

Variant	nsv872254
Chromosome Location	chr1:146503841-146544721
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:181)
CpG islands
(count:1099)
Chromatin interactive
region (count:28)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:181 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:146516435-146516446	K562	blood:	n/a	n/a
2	ATF3	chr1:146544653-146544913	K562	blood:	n/a	chr1:146544720-146544727
3	BATF	chr1:146544687-146544893	GM12878	blood:	n/a	n/a
4	BATF	chr1:146518478-146518756	GM12878	blood:	n/a	n/a
5	BATF	chr1:146518014-146518382	GM12878	blood:	n/a	n/a
6	BATF	chr1:146518027-146518369	GM12878	blood:	n/a	n/a
7	BATF	chr1:146544664-146544878	GM12878	blood:	n/a	n/a
8	BATF	chr1:146518484-146518763	GM12878	blood:	n/a	n/a
9	BCL11A	chr1:146518023-146518390	GM12878	blood:	n/a	n/a
10	BCL11A	chr1:146544653-146544883	GM12878	blood:	n/a	n/a
11	BCL11A	chr1:146544622-146544933	GM12878	blood:	n/a	n/a
12	BCL11A	chr1:146518060-146518399	GM12878	blood:	n/a	n/a
13	BHLHE40	chr1:146544054-146544163	K562	blood:	n/a	n/a
14	CEBPB	chr1:146544344-146544471	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr1:146504495-146504541	K562	blood:	n/a	n/a
16	CTCF	chr1:146525497-146525572	Kidney_OC	kidney:	n/a	n/a
17	CTCF	chr1:146506220-146506370	HBMEC	blood vessel:	n/a	n/a
18	CTCF	chr1:146518227-146518251	Spleen_OC	spleen:	n/a	n/a
19	E2F4	chr1:146519552-146519845	MCF10A-Er-Src	breast:	n/a	n/a
20	E2F6	chr1:146544317-146544457	K562	blood:	n/a	n/a
21	E2F6	chr1:146543761-146544859	H1-hESC	embryonic stem cell:	n/a	n/a
22	E2F6	chr1:146543984-146544167	K562	blood:	n/a	n/a
23	E2F6	chr1:146543920-146544639	H1-hESC	embryonic stem cell:	n/a	n/a
24	EBF1	chr1:146525002-146525104	GM12878	blood:	n/a	n/a
25	EBF1	chr1:146544697-146544889	GM12878	blood:	n/a	n/a
26	EBF1	chr1:146518172-146518653	GM12878	blood:	n/a	n/a
27	EBF1	chr1:146544705-146544900	GM12878	blood:	n/a	n/a
28	EBF1	chr1:146518058-146518657	GM12878	blood:	n/a	n/a
29	EBF1	chr1:146518085-146518457	GM12878	blood:	n/a	n/a
30	EP300	chr1:146518052-146518403	GM12878	blood:	n/a	chr1:146518199-146518213
31	EP300	chr1:146518094-146518624	GM12878	blood:	n/a	chr1:146518199-146518213 chr1:146518471-146518485
32	EP300	chr1:146544712-146544864	GM12878	blood:	n/a	n/a
33	EP300	chr1:146544647-146545022	GM12878	blood:	n/a	n/a
34	FOS	chr1:146517882-146518830	HUVEC	blood vessel:	n/a	chr1:146518066-146518075
35	FOS	chr1:146509161-146509590	HUVEC	blood vessel:	n/a	chr1:146509351-146509363
36	FOS	chr1:146518825-146518833	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr1:146542721-146542847	MCF10A-Er-Src	breast:	n/a	chr1:146542795-146542805 chr1:146542797-146542804 chr1:146542795-146542804
38	FOS	chr1:146518680-146518865	MCF10A-Er-Src	breast:	n/a	n/a
39	FOSL2	chr1:146544630-146544915	HepG2	liver:	n/a	n/a
40	FOSL2	chr1:146544692-146544911	HepG2	liver:	n/a	n/a
41	FOXA1	chr1:146544668-146544911	HepG2	liver:	n/a	n/a
42	FOXA1	chr1:146535662-146536100	HepG2	liver:	n/a	n/a
43	FOXA1	chr1:146535829-146536022	HepG2	liver:	n/a	n/a
44	FOXA2	chr1:146535700-146536189	A549	lung:	n/a	n/a
45	FOXA2	chr1:146533921-146534375	A549	lung:	n/a	n/a
46	FOXA2	chr1:146535714-146536032	A549	lung:	n/a	n/a
47	FOXM1	chr1:146518020-146518417	GM12878	blood:	n/a	n/a
48	GABPA	chr1:146544703-146544937	Hela-S3	cervix:	n/a	n/a
49	GATA2	chr1:146544693-146544892	K562	blood:	n/a	chr1:146544862-146544869
50	GATA2	chr1:146517877-146518340	HUVEC	blood vessel:	n/a	chr1:146518236-146518248

(count:1099 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:146525992-146526042	NHDF-neo	bronchial:	n/a
2	chr1:146525992-146526042	NHDF-neo	bronchial:	n/a
3	chr1:146543992-146544042	LNCaP	prostate:	n/a
4	chr1:146521800-146521850	HRE	kidney:	n/a
5	chr1:146522492-146522542	PANC-1	pancreas:	n/a
6	chr1:146525992-146526042	RPTEC	kidney:	n/a
7	chr1:146544645-146544695	SK-N-SH_RA	brain:	n/a
8	chr1:146533323-146533373	HepG2	liver:	n/a
9	chr1:146522878-146522928	Hela-S3	cervix:	n/a
10	chr1:146544044-146544094	SK-N-MC	brain:	n/a
11	chr1:146544044-146544094	PANC-1	pancreas:	n/a
12	chr1:146544267-146544317	SK-N-MC	brain:	n/a
13	chr1:146516011-146516061	HRE	kidney:	n/a
14	chr1:146516011-146516061	ovcar-3	ovarian:	n/a
15	chr1:146522554-146522604	AG04450	lung:	fetal
16	chr1:146522554-146522604	BE2_C	brain:	n/a
17	chr1:146521800-146521850	HEK293	kidney:	embryo
18	chr1:146515238-146515288	ovcar-3	ovarian:	n/a
19	chr1:146522492-146522542	GM06990	blood:	n/a
20	chr1:146522878-146522928	AG09319	gingival:	n/a
21	chr1:146544097-146544147	AG09309	skin:	n/a
22	chr1:146533323-146533373	HRPEpiC	eye:	n/a
23	chr1:146522492-146522542	GM19239	blood:	n/a
24	chr1:146543992-146544042	H1-hESC	embryonic stem cell:	embryo
25	chr1:146543596-146543646	GM12891	blood:	n/a
26	chr1:146522416-146522466	HepG2	liver:	n/a
27	chr1:146522554-146522604	GM06990	blood:	n/a
28	chr1:146543992-146544042	AG09309	skin:	n/a
29	chr1:146544044-146544094	Jurkat	blood:	n/a
30	chr1:146503900-146503950	HEEpiC	esophagus:	n/a
31	chr1:146544267-146544317	HRCEpiC	kidney:	n/a
32	chr1:146544044-146544094	GM12891	blood:	n/a
33	chr1:146503900-146503950	Jurkat	blood:	n/a
34	chr1:146543596-146543646	K562	blood:	n/a
35	chr1:146543596-146543646	HEEpiC	esophagus:	n/a
36	chr1:146503900-146503950	SKMC	muscle:	n/a
37	chr1:146544645-146544695	SAEC	small airway:	n/a
38	chr1:146519025-146519075	NHBE	bronchial:	n/a
39	chr1:146544267-146544317	IMR90	lung:	fetal
40	chr1:146533323-146533373	SK-N-SH	brain:	n/a
41	chr1:146544267-146544317	BE2_C	brain:	n/a
42	chr1:146522365-146522415	HCF	heart:	n/a
43	chr1:146522554-146522604	HNPCEpiC	eye:	n/a
44	chr1:146522878-146522928	HCT-116	colon:	n/a
45	chr1:146525992-146526042	AG04449	skin:	fetal
46	chr1:146543596-146543646	ovcar-3	ovarian:	n/a
47	chr1:146503900-146503950	HepG2	liver:	n/a
48	chr1:146525992-146526042	PFSK-1	brain:	n/a
49	chr1:146544267-146544317	NT2-D1	testis:	n/a
50	chr1:146533323-146533373	Hela-S3	cervix:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:146500894..146503604-chr1:146505375..146507725,2	MCF-7	breast:
2	chr1:146529795..146532554-chr1:146543290..146546177,2	MCF-7	breast:
3	chr1:146510052..146513278-chr1:146553511..146556367,3	MCF-7	breast:
4	chr1:146503324..146505730-chr1:146554828..146557692,2	K562	blood:
5	chr1:146529795..146532554-chr1:146543290..146546177,2	MCF-7	breast:
6	chr1:146518746..146520434-chr1:146527924..146529866,2	MCF-7	breast:
7	chr1:146518746..146520434-chr1:146527924..146529866,2	MCF-7	breast:
8	chr1:146542036..146544748-chr1:149223441..149225409,2	MCF-7	breast:
9	chr1:146512877..146514536-chr1:146516459..146518711,2	K562	blood:
10	chr1:146533488..146536910-chr1:146554170..146556510,5	K562	blood:
11	chr1:146505925..146509776-chr1:146553090..146557502,5	K562	blood:
12	chr1:146529272..146532255-chr1:146554616..146557776,4	K562	blood:
13	chr1:146532723..146535338-chr1:146554228..146556510,3	K562	blood:
14	chr1:146526066..146527690-chr1:146547733..146550722,2	MCF-7	breast:
15	chr1:146500715..146505145-chr1:146554885..146558544,5	MCF-7	breast:
16	chr1:146520193..146523021-chr1:146542603..146544431,2	MCF-7	breast:
17	chr1:144891445..144893339-chr1:146502271..146504240,2	MCF-7	breast:
18	chr1:146528515..146532214-chr1:146553802..146557776,4	K562	blood:
19	chr1:146505843..146507927-chr1:146554979..146557647,2	K562	blood:
20	chr1:146502664..146505503-chr1:146555291..146557477,4	MCF-7	breast:
21	chr1:146510544..146512904-chr1:146555893..146558120,2	K562	blood:
22	chr1:146512877..146514536-chr1:146516459..146518711,2	K562	blood:
23	chr1:146523530..146527862-chr1:146554112..146557348,5	K562	blood:
24	chr1:146524746..146527617-chr1:146553998..146556493,3	MCF-7	breast:
25	chr1:146527377..146530067-chr1:146546745..146548540,2	K562	blood:
26	chr1:146528549..146530712-chr1:146551544..146553259,2	K562	blood:
27	chr1:144890884..144894068-chr1:146500995..146504405,3	K562	blood:
28	chr1:146525668..146528622-chr1:146554429..146557542,4	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRKAB2-6	chr1:146542981-146543443	NONHSAT005993
2	lnc-PRKAB2-6	chr1:146544010-146544117	NONHSAT005993

No data

Variant related genes	Relation type
NBPF13P	TF binding region
ENSG00000225603	TF binding region
NBPF13P	CpG island
ENSG00000225603	CpG island
ENSG00000206737	chromatin interactions
ENSG00000225603	chromatin interactions
ENSG00000230832	chromatin interactions

Extended variants
information (count: 1836 )
Associated
traits (count: 157 )

Variant overlapped rSNPs/rCNVs (count:1836 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12141387	chr1:146503841-146503842	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs370444760	chr1:146503910-146503911	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs587622144	chr1:146503977-146503978	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs587698242	chr1:146503997-146503998	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs587757758	chr1:146504024-146504025	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs587651251	chr1:146504030-146504031	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs11240095	chr1:146504083-146504084	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs587764771	chr1:146504087-146504088	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs111860067	chr1:146504098-146504099	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs12122453	chr1:146504114-146504115	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs587737784	chr1:146504125-146504126	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs78957357	chr1:146504148-146504149	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs149512190	chr1:146504150-146504151	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs587666545	chr1:146504185-146504186	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs372224400	chr1:146504238-146504239	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs183397308	chr1:146504245-146504246	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs144026181	chr1:146504340-146504341	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs587657388	chr1:146504348-146504349	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs117290962	chr1:146504360-146504361	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs12122534	chr1:146504399-146504400	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs587665484	chr1:146504400-146504401	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs35319005	chr1:146504425-146504426	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs12139768	chr1:146504479-146504480	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs587620113	chr1:146504528-146504529	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs1853779	chr1:146504595-146504596	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs587699995	chr1:146504603-146504604	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs1853780	chr1:146504604-146504605	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs148285797	chr1:146504609-146504610	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs79918254	chr1:146504622-146504623	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs370177774	chr1:146504627-146504628	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs587635968	chr1:146504631-146504632	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs112637542	chr1:146504663-146504664	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs587685025	chr1:146504672-146504673	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs113010388	chr1:146504683-146504684	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs587609902	chr1:146504689-146504690	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs367651614	chr1:146504709-146504710	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs141328717	chr1:146504713-146504714	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs1853781	chr1:146504722-146504723	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs186656565	chr1:146504729-146504730	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs113685009	chr1:146504823-146504824	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs587729659	chr1:146504835-146504836	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs3862919	chr1:146504836-146504837	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs3862920	chr1:146504856-146504857	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs3851279	chr1:146504857-146504858	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs369105837	chr1:146504864-146504865	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs587610567	chr1:146504866-146504867	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs114680121	chr1:146504875-146504876	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs998672	chr1:146504878-146504879	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs3862921	chr1:146504890-146504891	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs587681545	chr1:146504899-146504900	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:157)

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
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
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
Tetralogy of Fallot	22912587	CNVD
Bladder cancer	21909424	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	17142309	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Anaplastic thyroid cancer	18753363	CNVD

Chromatin state (count:281 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:146494800-146504200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr1:146501600-146506800	Weak transcription	NHEK	skin
3	chr1:146503800-146504200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
4	chr1:146503800-146504600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
5	chr1:146504200-146504400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
6	chr1:146504200-146504600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr1:146504600-146508800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr1:146506800-146507600	Enhancers	NHEK	skin
9	chr1:146507400-146507800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr1:146508800-146509200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr1:146509200-146509400	Flanking Active TSS	HUVEC	blood vessel
12	chr1:146509200-146509600	Enhancers	Primary T cells from cord blood	blood
13	chr1:146509200-146509600	Enhancers	Primary hematopoietic stem cells short term culture	blood
14	chr1:146509200-146509600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr1:146509200-146509600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr1:146509400-146509600	Enhancers	HUVEC	blood vessel
17	chr1:146509600-146510400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr1:146509600-146515000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr1:146510400-146514800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr1:146512400-146513200	Active TSS	Primary T helper cells PMA-I stimulated	--
21	chr1:146512600-146513400	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr1:146512800-146513000	Enhancers	Primary B cells from peripheral blood	blood
23	chr1:146513000-146513200	Enhancers	Primary B cells from cord blood	blood
24	chr1:146513000-146514200	Weak transcription	Primary B cells from peripheral blood	blood
25	chr1:146513200-146513800	Active TSS	Primary T cells fromperipheralblood	blood
26	chr1:146513200-146514200	Weak transcription	Primary B cells from cord blood	blood
27	chr1:146513200-146514200	Weak transcription	Primary T helper cells PMA-I stimulated	--
28	chr1:146513400-146517800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
29	chr1:146514200-146514400	Active TSS	Primary T helper cells PMA-I stimulated	--
30	chr1:146514200-146521400	Enhancers	Primary B cells from cord blood	blood
31	chr1:146514200-146521800	Enhancers	Primary B cells from peripheral blood	blood
32	chr1:146514400-146514600	Weak transcription	Primary T helper cells PMA-I stimulated	--
33	chr1:146514600-146514800	Enhancers	Primary T helper cells PMA-I stimulated	--
34	chr1:146514800-146515000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
35	chr1:146514800-146517800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr1:146515000-146515800	Enhancers	Primary T helper cells PMA-I stimulated	--
37	chr1:146515000-146518400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr1:146515000-146520400	Enhancers	Primary hematopoietic stem cells	blood
39	chr1:146515200-146515400	Enhancers	Primary T killer memory cells from peripheral blood	blood
40	chr1:146515800-146516800	Weak transcription	Primary T helper cells PMA-I stimulated	--
41	chr1:146515800-146519000	Enhancers	Primary hematopoietic stem cells short term culture	blood
42	chr1:146516000-146517800	Enhancers	Dnd41	blood
43	chr1:146516600-146516800	Enhancers	Primary T helper cells fromperipheralblood	blood
44	chr1:146516600-146517200	Enhancers	GM12878-XiMat	blood
45	chr1:146516800-146517000	Enhancers	Primary T helper cells PMA-I stimulated	--
46	chr1:146516800-146517400	Weak transcription	Primary T helper cells fromperipheralblood	blood
47	chr1:146516800-146520200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
48	chr1:146517000-146517400	Weak transcription	Primary T helper cells PMA-I stimulated	--
49	chr1:146517200-146517600	Weak transcription	GM12878-XiMat	blood
50	chr1:146517400-146518400	Enhancers	Primary T helper cells PMA-I stimulated	--

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