Variant report

Variant	nsv8213
Chromosome Location	chr1:10450914-10460439
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:724)
CpG islands
(count:1038)
Chromatin interactive
region (count:24)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:724 , 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	ARID3A	chr1:10458757-10459497	K562	blood:	n/a	n/a
2	ARID3A	chr1:10458715-10459371	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:10460401-10460924	K562	blood:	n/a	n/a
4	ATF1	chr1:10458604-10459266	K562	blood:	n/a	n/a
5	ATF2	chr1:10458621-10459244	GM12878	blood:	n/a	n/a
6	ATF2	chr1:10458748-10459054	GM12878	blood:	n/a	n/a
7	ATF2	chr1:10458491-10459059	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr1:10458953-10459327	A549	lung:	n/a	n/a
9	BACH1	chr1:10458808-10459091	K562	blood:	n/a	n/a
10	BACH1	chr1:10457177-10457183	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr1:10458657-10459987	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr1:10458714-10458998	GM12878	blood:	n/a	n/a
13	BCL3	chr1:10458618-10459429	A549	lung:	n/a	n/a
14	BCL3	chr1:10459522-10459847	A549	lung:	n/a	n/a
15	BCL3	chr1:10458434-10459386	A549	lung:	n/a	n/a
16	BCLAF1	chr1:10458513-10459189	GM12878	blood:	n/a	n/a
17	BHLHE40	chr1:10458606-10459843	GM12878	blood:	n/a	chr1:10459357-10459373
18	BHLHE40	chr1:10458547-10460008	K562	blood:	n/a	chr1:10459357-10459373
19	BHLHE40	chr1:10458545-10459668	HepG2	liver:	n/a	chr1:10459357-10459373
20	BRCA1	chr1:10458476-10459205	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr1:10458508-10458558	HepG2	liver:	n/a	n/a
22	BRCA1	chr1:10459142-10459321	GM12878	blood:	n/a	n/a
23	BRCA1	chr1:10458762-10459237	HepG2	liver:	n/a	n/a
24	BRCA1	chr1:10458736-10458930	GM12878	blood:	n/a	n/a
25	BRCA1	chr1:10459135-10459271	H1-hESC	embryonic stem cell:	n/a	n/a
26	CBX3	chr1:10458371-10460523	K562	blood:	n/a	n/a
27	CBX3	chr1:10454296-10454614	K562	blood:	n/a	n/a
28	CCNT2	chr1:10458543-10459871	K562	blood:	n/a	chr1:10459500-10459509 chr1:10458635-10458644
29	CEBPB	chr1:10458745-10459257	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr1:10458716-10459226	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr1:10460414-10460994	K562	blood:	n/a	chr1:10460753-10460766 chr1:10460753-10460764
32	CEBPB	chr1:10458855-10459062	K562	blood:	n/a	n/a
33	CEBPD	chr1:10458664-10459625	HepG2	liver:	n/a	n/a
34	CHD1	chr1:10459579-10460126	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD1	chr1:10460038-10460077	GM12878	blood:	n/a	n/a
36	CHD1	chr1:10459604-10459789	GM12878	blood:	n/a	n/a
37	CHD1	chr1:10459255-10459320	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD2	chr1:10459514-10459515	HepG2	liver:	n/a	n/a
39	CHD2	chr1:10458678-10459240	HepG2	liver:	n/a	n/a
40	CHD2	chr1:10458501-10459353	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD2	chr1:10458648-10459256	K562	blood:	n/a	n/a
42	CHD2	chr1:10458653-10459641	GM12878	blood:	n/a	chr1:10459392-10459402
43	CHD2	chr1:10459690-10459713	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD2	chr1:10458437-10459692	Hela-S3	cervix:	n/a	chr1:10459392-10459402
45	CHD2	chr1:10459553-10459756	K562	blood:	n/a	n/a
46	CREB1	chr1:10458535-10459885	H1-hESC	embryonic stem cell:	n/a	n/a
47	CREB1	chr1:10458462-10459664	K562	blood:	n/a	n/a
48	CREB1	chr1:10458546-10459604	A549	lung:	n/a	n/a
49	CREB1	chr1:10458416-10459881	H1-hESC	embryonic stem cell:	n/a	n/a
50	CREB1	chr1:10458792-10459258	ECC-1	luminal epithelium:	n/a	n/a

(count:1038 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:10455147-10455197	U87	brain:	n/a
2	chr1:10455147-10455197	U87	brain:	n/a
3	chr1:10459003-10459053	IMR90	lung:	fetal
4	chr1:10458942-10458992	U87	brain:	n/a
5	chr1:10458942-10458992	HCT-116	colon:	n/a
6	chr1:10458441-10458491	H1-hESC	embryonic stem cell:	embryo
7	chr1:10458599-10458649	ovcar-3	ovarian:	n/a
8	chr1:10459003-10459053	PrEC	prostate:	n/a
9	chr1:10459695-10459745	GM12891	blood:	n/a
10	chr1:10458905-10458955	AG09309	skin:	n/a
11	chr1:10459695-10459745	HPAEpiC	pulmonary alveolar:	n/a
12	chr1:10460205-10460255	PFSK-1	brain:	n/a
13	chr1:10459140-10459190	ECC-1	luminal epithelium:	n/a
14	chr1:10458599-10458649	GM19239	blood:	n/a
15	chr1:10459573-10459623	MCF10A-Er-Src	breast:	n/a
16	chr1:10459573-10459623	H1-hESC	embryonic stem cell:	embryo
17	chr1:10459268-10459318	A549	lung:	n/a
18	chr1:10459146-10459196	A549	lung:	n/a
19	chr1:10458832-10458882	MCF-7	breast:	n/a
20	chr1:10458441-10458491	SAEC	small airway:	n/a
21	chr1:10459268-10459318	MCF10A-Er-Src	breast:	n/a
22	chr1:10459268-10459318	SK-N-SH	brain:	n/a
23	chr1:10458441-10458491	BJ	skin:	n/a
24	chr1:10459695-10459745	HCF	heart:	n/a
25	chr1:10455147-10455197	AoSMC	blood vessel:	n/a
26	chr1:10459003-10459053	BJ	skin:	n/a
27	chr1:10459268-10459318	T-47D	breast:	n/a
28	chr1:10459573-10459623	U87	brain:	n/a
29	chr1:10459140-10459190	Hela-S3	cervix:	n/a
30	chr1:10459003-10459053	LNCaP	prostate:	n/a
31	chr1:10458905-10458955	HCPEpiC	choroid plexus:	n/a
32	chr1:10458942-10458992	HRE	kidney:	n/a
33	chr1:10459268-10459318	NB4	blood:	n/a
34	chr1:10459003-10459053	GM19239	blood:	n/a
35	chr1:10458942-10458992	HCPEpiC	choroid plexus:	n/a
36	chr1:10458832-10458882	NB4	blood:	n/a
37	chr1:10459003-10459053	HCM	heart:	n/a
38	chr1:10460205-10460255	NHBE	bronchial:	n/a
39	chr1:10458939-10458989	HCT-116	colon:	n/a
40	chr1:10459003-10459053	Hela-S3	cervix:	n/a
41	chr1:10459140-10459190	CMK	blood:	n/a
42	chr1:10459052-10459102	NH-A	brain:	n/a
43	chr1:10459573-10459623	A549	lung:	n/a
44	chr1:10458905-10458955	NHDF-neo	bronchial:	n/a
45	chr1:10458832-10458882	PFSK-1	brain:	n/a
46	chr1:10460205-10460255	HAEpiC	amniotic membrane:	n/a
47	chr1:10459268-10459318	AG09319	gingival:	n/a
48	chr1:10458942-10458992	GM06990	blood:	n/a
49	chr1:10459003-10459053	Hepatocyte	liver:	n/a
50	chr1:10455147-10455197	HPAEpiC	pulmonary alveolar:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:10458656..10459252-chr5:137089631..137090531,2	Hela-S3	cervix:
2	chr1:10447080..10448885-chr1:10454434..10456655,2	MCF-7	breast:
3	chr1:10456887..10459867-chr1:10534957..10536960,2	K562	blood:
4	chr1:10269508..10272201-chr1:10459062..10462119,3	K562	blood:
5	chr1:10447111..10452516-chr1:10455817..10460024,9	K562	blood:
6	chr1:10457843..10460253-chr1:10533493..10537083,3	MCF-7	breast:
7	chr1:10457403..10461622-chr1:10531171..10536559,7	K562	blood:
8	chr1:10446221..10450110-chr1:10457451..10462205,13	MCF-7	breast:
9	chr1:10449520..10451785-chr1:10471449..10473119,2	K562	blood:
10	chr1:10446950..10451985-chr1:10457311..10462205,6	K562	blood:
11	chr1:10457797..10461098-chr1:10474071..10478087,9	K562	blood:
12	chr1:10446399..10450088-chr1:10457513..10461303,7	MCF-7	breast:
13	chr1:10269636..10272138-chr1:10457591..10460138,4	K562	blood:
14	chr1:10451777..10453446-chr1:10457951..10460281,3	MCF-7	breast:
15	chr1:10001846..10004168-chr1:10458912..10460649,2	K562	blood:
16	chr1:10457490..10461716-chr1:10469511..10473951,6	K562	blood:
17	chr1:9882661..9885013-chr1:10458252..10460185,2	K562	blood:
18	chr1:10457879..10460190-chr8:103875742..103877594,2	MCF-7	breast:
19	chr1:10457794..10461321-chr1:10487053..10491931,7	K562	blood:
20	chr1:10448474..10450056-chr1:10452189..10454390,3	K562	blood:
21	chr1:10457794..10460664-chr1:10487844..10492697,5	K562	blood:
22	chr1:10447111..10452516-chr1:10455817..10460024,9	K562	blood:
23	chr1:10458808..10459803-chr11:8710259..8711120,2	HCT-116	colon:
24	chr1:10446950..10451985-chr1:10457311..10462205,6	K562	blood:

No data

Variant related genes	Relation type
PGD	TF binding region
PGD	CpG island
ENSG00000162441	chromatin interactions
ENSG00000228150	chromatin interactions
ENSG00000166441	chromatin interactions
ENSG00000142657	chromatin interactions
ENSG00000253320	chromatin interactions
ENSG00000142655	chromatin interactions
ENSG00000054523	chromatin interactions
ENSG00000265945	chromatin interactions
ENSG00000251503	chromatin interactions
ENSG00000171603	chromatin interactions
ENSG00000155096	chromatin interactions
ENSG00000271989	chromatin interactions
ENSG00000177733	chromatin interactions
ENSG00000175279	chromatin interactions
ENSG00000160049	chromatin interactions
ENSG00000173614	chromatin interactions

Extended variants
information (count: 390 )
Associated
traits (count: 116 )

Variant overlapped rSNPs/rCNVs (count:390 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535332951	chr1:10450923-10450924	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs188606336	chr1:10450930-10450931	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs569027547	chr1:10450950-10450951	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs537186894	chr1:10450969-10450970	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs12143395	chr1:10451036-10451037	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs2847342	chr1:10451078-10451079	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs577220329	chr1:10451080-10451081	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs113259459	chr1:10451181-10451182	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs528622546	chr1:10451186-10451187	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs143071568	chr1:10451190-10451191	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs553368987	chr1:10451238-10451239	Weak transcription Enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs193167899	chr1:10451272-10451273	Weak transcription Enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs542519972	chr1:10451273-10451274	Weak transcription Enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs563776190	chr1:10451299-10451300	Weak transcription Enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs185049614	chr1:10451405-10451406	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs560343177	chr1:10451411-10451412	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs60661947	chr1:10451425-10451426	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs58867993	chr1:10451426-10451427	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs371147621	chr1:10451475-10451476	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs190154159	chr1:10451507-10451508	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs564213552	chr1:10451508-10451509	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs532161161	chr1:10451523-10451524	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs111777265	chr1:10451549-10451550	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs528148605	chr1:10451565-10451566	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs191823014	chr1:10451566-10451567	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs11578694	chr1:10451582-10451583	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs374300341	chr1:10451608-10451609	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs529193767	chr1:10451628-10451629	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs550840100	chr1:10451652-10451653	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs183950512	chr1:10451694-10451695	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs527903214	chr1:10451707-10451708	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs368935775	chr1:10451715-10451716	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs539621208	chr1:10451719-10451720	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs555169013	chr1:10451738-10451739	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs34259657	chr1:10451739-10451740	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs71274810	chr1:10451758-10451759	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs4846217	chr1:10451799-10451800	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs188332352	chr1:10451809-10451810	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs535106004	chr1:10451822-10451823	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs536374500	chr1:10451854-10451855	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs554657617	chr1:10451966-10451967	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs553432288	chr1:10451968-10451969	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs4846218	chr1:10452040-10452041	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs59761387	chr1:10452049-10452050	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs180686330	chr1:10452051-10452052	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs543272711	chr1:10452064-10452065	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs538856926	chr1:10452085-10452086	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs563699734	chr1:10452086-10452087	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs557645867	chr1:10452124-10452125	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs144390104	chr1:10452162-10452163	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:116)

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
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

Chromatin state (count:545 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:10438600-10458200	Weak transcription	Right Atrium	heart
2	chr1:10439600-10458200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr1:10440000-10451800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr1:10440000-10458400	Weak transcription	Lung	lung
5	chr1:10444800-10458200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr1:10445600-10454000	Weak transcription	Fetal Brain Female	brain
7	chr1:10447800-10454000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr1:10447800-10458400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr1:10448200-10452800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr1:10448200-10454200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr1:10448200-10458200	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr1:10448200-10458200	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr1:10448200-10458400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr1:10448400-10454400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
15	chr1:10448600-10451200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr1:10448600-10453800	Weak transcription	Fetal Stomach	stomach
17	chr1:10448600-10454200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr1:10448600-10454800	Weak transcription	HUES48 Cell Line	embryonic stem cell
19	chr1:10448600-10458200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
20	chr1:10448600-10458200	Weak transcription	Brain Angular Gyrus	brain
21	chr1:10448600-10458400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr1:10448600-10458400	Weak transcription	HSMM	muscle
23	chr1:10448800-10453400	Strong transcription	Cortex derived primary cultured neurospheres	brain
24	chr1:10448800-10458200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr1:10448800-10458200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
26	chr1:10448800-10458200	Weak transcription	Stomach Smooth Muscle	stomach
27	chr1:10448800-10458200	Weak transcription	HUVEC	blood vessel
28	chr1:10448800-10458200	Weak transcription	NH-A	brain
29	chr1:10448800-10458200	Weak transcription	NHEK	skin
30	chr1:10449000-10451800	Enhancers	Primary B cells from cord blood	blood
31	chr1:10449000-10452600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr1:10449000-10453800	Weak transcription	HUES6 Cell Line	embryonic stem cell
33	chr1:10449000-10454000	Weak transcription	Brain Substantia Nigra	brain
34	chr1:10449000-10458200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr1:10449000-10458200	Weak transcription	Brain Anterior Caudate	brain
36	chr1:10449000-10458200	Weak transcription	Fetal Intestine Large	intestine
37	chr1:10449000-10458200	Weak transcription	Rectal Mucosa Donor 29	rectum
38	chr1:10449000-10458200	Weak transcription	Thymus	Thymus
39	chr1:10449000-10458200	Weak transcription	HSMMtube	muscle
40	chr1:10449200-10458200	Weak transcription	Brain Cingulate Gyrus	brain
41	chr1:10449200-10458200	Weak transcription	Fetal Muscle Leg	muscle
42	chr1:10449200-10458400	Weak transcription	Sigmoid Colon	Sigmoid Colon
43	chr1:10449600-10451000	Enhancers	Monocytes-CD14+_RO01746	blood
44	chr1:10449600-10454000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr1:10449600-10457400	Weak transcription	Brain Hippocampus Middle	brain
46	chr1:10449600-10458200	Weak transcription	Esophagus	oesophagus
47	chr1:10449600-10458200	Weak transcription	Pancreas	Pancrea
48	chr1:10449600-10458200	Weak transcription	Hela-S3	cervix
49	chr1:10449800-10451000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr1:10449800-10453800	Weak transcription	Fetal Intestine Small	intestine

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