Variant report

Variant	nsv871898
Chromosome Location	chr1:70681486-70723347
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1096)
CpG islands
(count:733)
Chromatin interactive
region (count:50)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1096 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:70686778-70687628	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:70685713-70686118	K562	blood:	n/a	n/a
3	ARID3A	chr1:70687392-70687436	K562	blood:	n/a	n/a
4	ATF1	chr1:70685744-70686062	K562	blood:	n/a	n/a
5	ATF1	chr1:70686896-70687222	K562	blood:	n/a	n/a
6	ATF2	chr1:70686837-70687147	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr1:70687416-70687795	GM12878	blood:	n/a	n/a
8	ATF2	chr1:70687385-70687790	GM12878	blood:	n/a	n/a
9	ATF2	chr1:70686755-70687325	GM12878	blood:	n/a	n/a
10	ATF2	chr1:70686740-70687470	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF3	chr1:70686879-70687149	K562	blood:	n/a	n/a
12	BACH1	chr1:70697205-70697461	K562	blood:	n/a	n/a
13	BACH1	chr1:70686894-70687290	H1-hESC	embryonic stem cell:	n/a	n/a
14	BCL3	chr1:70686713-70687297	A549	lung:	n/a	n/a
15	BCL3	chr1:70686837-70687516	GM12878	blood:	n/a	n/a
16	BCLAF1	chr1:70686816-70687458	GM12878	blood:	n/a	n/a
17	BCLAF1	chr1:70686739-70687982	GM12878	blood:	n/a	n/a
18	BHLHE40	chr1:70686858-70687634	HepG2	liver:	n/a	chr1:70686984-70687000
19	BHLHE40	chr1:70686799-70687516	K562	blood:	n/a	chr1:70686984-70687000
20	BHLHE40	chr1:70686401-70686402	K562	blood:	n/a	n/a
21	BHLHE40	chr1:70686877-70687692	GM12878	blood:	n/a	chr1:70686984-70687000
22	BRCA1	chr1:70686808-70687483	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr1:70685818-70685975	GM12878	blood:	n/a	n/a
24	BRCA1	chr1:70686971-70687296	GM12878	blood:	n/a	n/a
25	BRCA1	chr1:70684043-70684214	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr1:70687025-70687251	HepG2	liver:	n/a	n/a
27	CBX3	chr1:70686754-70687637	K562	blood:	n/a	n/a
28	CCNT2	chr1:70685555-70685909	K562	blood:	n/a	n/a
29	CCNT2	chr1:70686834-70687548	K562	blood:	n/a	chr1:70687133-70687142
30	CEBPB	chr1:70687307-70687366	K562	blood:	n/a	n/a
31	CEBPB	chr1:70685203-70685359	Hela-S3	cervix:	n/a	chr1:70685254-70685265
32	CEBPB	chr1:70695269-70695591	A549	lung:	n/a	chr1:70695562-70695575 chr1:70695420-70695433 chr1:70695421-70695432
33	CEBPB	chr1:70715065-70715344	HepG2	liver:	n/a	chr1:70715223-70715234
34	CEBPB	chr1:70720247-70720439	HepG2	liver:	n/a	n/a
35	CEBPB	chr1:70686915-70687340	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr1:70720237-70720446	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr1:70688421-70688678	HepG2	liver:	n/a	chr1:70688562-70688575
38	CEBPB	chr1:70685131-70685398	IMR90	lung:	n/a	chr1:70685254-70685265
39	CEBPB	chr1:70720251-70720430	K562	blood:	n/a	n/a
40	CEBPB	chr1:70722595-70722871	K562	blood:	n/a	n/a
41	CEBPB	chr1:70695273-70695573	K562	blood:	n/a	chr1:70695420-70695433 chr1:70695421-70695432
42	CEBPB	chr1:70715078-70715328	IMR90	lung:	n/a	chr1:70715223-70715234
43	CEBPB	chr1:70695262-70695608	HepG2	liver:	n/a	chr1:70695562-70695575 chr1:70695420-70695433 chr1:70695421-70695432
44	CEBPB	chr1:70685089-70685428	HepG2	liver:	n/a	chr1:70685254-70685265
45	CEBPB	chr1:70695292-70695589	IMR90	lung:	n/a	chr1:70695562-70695575 chr1:70695420-70695433 chr1:70695421-70695432
46	CEBPD	chr1:70686877-70687334	HepG2	liver:	n/a	n/a
47	CHD1	chr1:70686641-70688036	GM12878	blood:	n/a	n/a
48	CHD1	chr1:70686554-70688839	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr1:70686822-70687719	Hela-S3	cervix:	n/a	n/a
50	CHD2	chr1:70686857-70687628	GM12878	blood:	n/a	n/a

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:70684371-70684421	MCF-7	breast:	n/a
2	chr1:70684371-70684421	MCF-7	breast:	n/a
3	chr1:70687506-70687556	SK-N-SH	brain:	n/a
4	chr1:70687106-70687156	GM12891	blood:	n/a
5	chr1:70691524-70691574	MCF-7	breast:	n/a
6	chr1:70687106-70687156	HL-60	blood:	n/a
7	chr1:70687559-70687609	U87	brain:	n/a
8	chr1:70687559-70687609	A549	lung:	n/a
9	chr1:70710389-70710439	MCF10A-Er-Src	breast:	n/a
10	chr1:70710389-70710439	GM06990	blood:	n/a
11	chr1:70715648-70715698	HAEpiC	amniotic membrane:	n/a
12	chr1:70710422-70710472	HEEpiC	esophagus:	n/a
13	chr1:70710422-70710472	H1-hESC	embryonic stem cell:	embryo
14	chr1:70715648-70715698	GM12892	blood:	n/a
15	chr1:70687124-70687174	SK-N-SH_RA	brain:	n/a
16	chr1:70687080-70687130	RPTEC	kidney:	n/a
17	chr1:70687106-70687156	H1-hESC	embryonic stem cell:	embryo
18	chr1:70687559-70687609	CMK	blood:	n/a
19	chr1:70710389-70710439	ProgFib	skin:	n/a
20	chr1:70715648-70715698	Jurkat	blood:	n/a
21	chr1:70691524-70691574	GM12891	blood:	n/a
22	chr1:70684371-70684421	A549	lung:	n/a
23	chr1:70687415-70687465	ECC-1	luminal epithelium:	n/a
24	chr1:70687080-70687130	GM12891	blood:	n/a
25	chr1:70687415-70687465	GM12892	blood:	n/a
26	chr1:70687301-70687351	BE2_C	brain:	n/a
27	chr1:70687415-70687465	HEK293	kidney:	embryo
28	chr1:70710389-70710439	RPTEC	kidney:	n/a
29	chr1:70687124-70687174	NH-A	brain:	n/a
30	chr1:70687106-70687156	HCM	heart:	n/a
31	chr1:70687080-70687130	AG09319	gingival:	n/a
32	chr1:70684371-70684421	Hela-S3	cervix:	n/a
33	chr1:70691524-70691574	Hepatocyte	liver:	n/a
34	chr1:70687106-70687156	CMK	blood:	n/a
35	chr1:70687415-70687465	A549	lung:	n/a
36	chr1:70687106-70687156	GM12878	blood:	n/a
37	chr1:70691524-70691574	IMR90	lung:	fetal
38	chr1:70687124-70687174	AG09319	gingival:	n/a
39	chr1:70687559-70687609	HL-60	blood:	n/a
40	chr1:70687415-70687465	Jurkat	blood:	n/a
41	chr1:70687106-70687156	AG09309	skin:	n/a
42	chr1:70687559-70687609	HPAEpiC	pulmonary alveolar:	n/a
43	chr1:70687080-70687130	HL-60	blood:	n/a
44	chr1:70715648-70715698	LNCaP	prostate:	n/a
45	chr1:70687124-70687174	NT2-D1	testis:	n/a
46	chr1:70715648-70715698	AoSMC	blood vessel:	n/a
47	chr1:70687301-70687351	SKMC	muscle:	n/a
48	chr1:70687301-70687351	HEEpiC	esophagus:	n/a
49	chr1:70687559-70687609	SK-N-SH_RA	brain:	n/a
50	chr1:70687415-70687465	NH-A	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr1:70686799..70688622-chr1:70819236..70822047,3	K562	blood:
2	chr1:70684364..70687178-chr1:70692446..70695041,2	MCF-7	breast:
3	chr1:70686741..70687626-chr16:29827433..29828123,2	Hela-S3	cervix:
4	chr1:70676847..70678967-chr1:70704287..70707286,2	MCF-7	breast:
5	chr1:70686774..70687532-chr11:76091229..76092168,2	HCT-116	colon:
6	chr1:70704895..70706743-chr1:70713115..70715571,2	MCF-7	breast:
7	chr1:70690841..70693656-chr1:70712406..70716408,4	K562	blood:
8	chr1:70714159..70717525-chr1:70719321..70722644,5	K562	blood:
9	chr1:70699386..70701238-chr1:70744306..70747139,2	K562	blood:
10	chr1:70698613..70700864-chr1:70712047..70714516,2	K562	blood:
11	chr1:70691837..70693690-chr1:70781962..70783731,2	K562	blood:
12	chr1:70667153..70674800-chr1:70681943..70693478,26	K562	blood:
13	chr1:70669364..70673005-chr1:70681293..70684159,5	K562	blood:
14	chr1:70680332..70681916-chr1:70685597..70687772,2	MCF-7	breast:
15	chr1:70705684..70710754-chr1:70711128..70717552,6	K562	blood:
16	chr1:70668667..70673217-chr1:70684547..70688689,8	K562	blood:
17	chr1:70679382..70681987-chr1:70682758..70684789,3	K562	blood:
18	chr1:70671444..70673368-chr1:70706387..70708615,2	K562	blood:
19	chr1:70709756..70712647-chr1:71546604..71549117,2	MCF-7	breast:
20	chr1:70687323..70689346-chr1:70692516..70694332,3	MCF-7	breast:
21	chr1:70717775..70720172-chr1:70724645..70726966,2	K562	blood:
22	chr1:70679382..70681987-chr1:70682758..70684789,3	K562	blood:
23	chr1:70688440..70690850-chr1:70877083..70879333,2	K562	blood:
24	chr1:70714127..70716625-chr1:70718344..70722644,5	K562	blood:
25	chr1:70690194..70693110-chr1:70772753..70775116,2	K562	blood:
26	chr1:70669751..70673129-chr1:70685079..70688457,4	MCF-7	breast:
27	chr1:70686750..70687728-chr17:48784876..48785472,2	Hela-S3	cervix:
28	chr1:70697900..70700190-chr1:70817863..70820129,2	MCF-7	breast:
29	chr1:70671321..70673336-chr1:70700811..70702610,2	K562	blood:
30	chr1:70643607..70646837-chr1:70686224..70688710,3	K562	blood:
31	chr1:70679935..70684301-chr1:70685237..70690690,9	K562	blood:
32	chr1:70694395..70695957-chr1:70712165..70714538,2	K562	blood:
33	chr1:70669146..70671967-chr1:70689438..70693050,5	K562	blood:
34	chr1:70692896..70695423-chr1:70718003..70720357,3	K562	blood:
35	chr1:70606579..70609498-chr1:70685222..70687844,2	K562	blood:
36	chr1:70687323..70689346-chr1:70692516..70694332,3	MCF-7	breast:
37	chr1:70686799..70689606-chr1:70818481..70820974,3	K562	blood:
38	chr1:70694395..70695957-chr1:70712165..70714538,2	K562	blood:
39	chr1:70705179..70706922-chr1:70760768..70763689,2	K562	blood:
40	chr1:70719944..70722820-chr1:70729283..70730801,2	K562	blood:
41	chr1:70688424..70691720-chr1:70692048..70694571,6	MCF-7	breast:
42	chr1:70685268..70690578-chr1:70702989..70707451,6	MCF-7	breast:
43	chr1:70670478..70672427-chr1:70697851..70699860,2	K562	blood:
44	chr1:70684364..70687178-chr1:70692446..70695041,2	MCF-7	breast:
45	chr1:70685799..70687948-chr1:70819964..70821804,2	MCF-7	breast:
46	chr1:70687235..70688815-chr1:70690103..70691870,2	MCF-7	breast:
47	chr1:70686924..70688596-chr1:70820161..70821739,2	MCF-7	breast:
48	chr1:70687006..70687600-chr1:212208863..212209612,2	Hela-S3	cervix:
49	chr1:70685268..70690578-chr1:70702989..70707451,6	MCF-7	breast:
50	chr1:70670643..70672906-chr1:70684026..70686642,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRRC7-5	chr1:70696778-70696957	NONHSAT003849
2	lnc-LRRC40-1	chr1:70684272-70684527	ENSG00000228988.1
3	lnc-LRRC40-1	chr1:70686506-70686706	ENSG00000228988.1
4	lnc-LRRC7-5	chr1:70695747-70696301	NONHSAT003849

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	SFRS11	hsa-miR-376a-3p	chr1:70716778-70716802

Variant related genes	Relation type
SRSF11	TF binding region
ENSG00000228988	TF binding region
SRSF11	CpG island
ENSG00000228988	CpG island
ENSG00000118454	chromatin interactions
ENSG00000143493	chromatin interactions
ENSG00000137492	chromatin interactions
ENSG00000143476	chromatin interactions
ENSG00000116754	chromatin interactions
ENSG00000229956	chromatin interactions
ENSG00000066557	chromatin interactions
ENSG00000132485	chromatin interactions
ENSG00000244389	chromatin interactions
ENSG00000033122	chromatin interactions
ENSG00000263136	chromatin interactions
ENSG00000154945	chromatin interactions
ENSG00000197568	chromatin interactions
ENSG00000228988	chromatin interactions

Extended variants
information (count: 1547 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:1547 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12565362	chr1:70681486-70681487	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs571527271	chr1:70681487-70681488	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs192598128	chr1:70681495-70681496	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs540476165	chr1:70681533-70681534	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs553748757	chr1:70681545-70681546	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs184576354	chr1:70681554-70681555	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs187704216	chr1:70681583-70681584	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs543379546	chr1:70681618-70681619	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs141739302	chr1:70681669-70681670	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs192776443	chr1:70681696-70681697	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs146274174	chr1:70681697-70681698	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs564839856	chr1:70681716-70681717	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs527333889	chr1:70681721-70681722	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs557321029	chr1:70681741-70681742	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs577002258	chr1:70681748-70681749	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs529822872	chr1:70681749-70681750	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs376091660	chr1:70681762-70681763	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs545572257	chr1:70681833-70681834	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs537865341	chr1:70681848-70681849	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs551709907	chr1:70681869-70681870	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs72929219	chr1:70681888-70681889	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs534335113	chr1:70681912-70681913	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs554295316	chr1:70681916-70681917	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs139178084	chr1:70681941-70681942	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs551226152	chr1:70681943-70681944	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs149987203	chr1:70681946-70681947	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs201425933	chr1:70681958-70681959	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs386632240	chr1:70681985-70681986	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs148711784	chr1:70681987-70681988	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs544682354	chr1:70682035-70682036	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs564943461	chr1:70682064-70682065	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs571938239	chr1:70682103-70682104	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs552059564	chr1:70682109-70682110	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs71921219	chr1:70682118-70682119	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs538577898	chr1:70682119-70682120	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs78710662	chr1:70682132-70682133	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs553076135	chr1:70682189-70682190	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs560626301	chr1:70682236-70682237	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs529860901	chr1:70682313-70682314	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs716241	chr1:70682319-70682320	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs549528349	chr1:70682364-70682365	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs563441923	chr1:70682406-70682407	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs716240	chr1:70682414-70682415	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs144758044	chr1:70682428-70682429	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs35608988	chr1:70682465-70682466	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs147901007	chr1:70682467-70682468	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs534242447	chr1:70682511-70682512	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs571652352	chr1:70682513-70682514	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs184348390	chr1:70682517-70682518	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs11581894	chr1:70682550-70682551	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:105)

Disease	PMID	Source
Medulloblastoma	21979893	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
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	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
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	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
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	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
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal cancer	21851588	CNVD
abnormal development	18461090	CNVD
Ewing''s sarcoma	17952124	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1521 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:70672000-70686200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr1:70672000-70687000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr1:70672400-70686800	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr1:70672600-70686400	Weak transcription	Primary neutrophils fromperipheralblood	blood
5	chr1:70672600-70686600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr1:70672800-70686600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr1:70673000-70681800	Weak transcription	Fetal Kidney	kidney
8	chr1:70673000-70683400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr1:70673200-70686200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr1:70673200-70686200	Weak transcription	Rectal Mucosa Donor 29	rectum
11	chr1:70673200-70686400	Weak transcription	Brain Substantia Nigra	brain
12	chr1:70673200-70686400	Weak transcription	HSMMtube	muscle
13	chr1:70673200-70686600	Weak transcription	NH-A	brain
14	chr1:70673400-70686200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr1:70673400-70686200	Weak transcription	HMEC	breast
16	chr1:70673400-70686400	Weak transcription	Fetal Brain Male	brain
17	chr1:70673400-70686600	Weak transcription	A549	lung
18	chr1:70673600-70686400	Weak transcription	Brain Cingulate Gyrus	brain
19	chr1:70673800-70686000	Weak transcription	Rectal Smooth Muscle	rectum
20	chr1:70673800-70686600	Weak transcription	Brain Hippocampus Middle	brain
21	chr1:70673800-70687200	Weak transcription	Small Intestine	intestine
22	chr1:70674200-70685800	Weak transcription	Right Ventricle	heart
23	chr1:70674200-70686600	Weak transcription	Brain Angular Gyrus	brain
24	chr1:70674200-70686600	Weak transcription	Brain Anterior Caudate	brain
25	chr1:70674200-70686800	Weak transcription	Aorta	Aorta
26	chr1:70674400-70686200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr1:70674400-70686400	Weak transcription	Duodenum Smooth Muscle	Duodenum
28	chr1:70674400-70686600	Weak transcription	H1 Cell Line	embryonic stem cell
29	chr1:70674400-70686600	Weak transcription	Colonic Mucosa	Colon
30	chr1:70674400-70686600	Weak transcription	Colon Smooth Muscle	Colon
31	chr1:70674600-70686400	Weak transcription	HUES6 Cell Line	embryonic stem cell
32	chr1:70674600-70686600	Weak transcription	HUES48 Cell Line	embryonic stem cell
33	chr1:70675000-70682600	Weak transcription	HSMM	muscle
34	chr1:70675000-70685600	Weak transcription	Skeletal Muscle Male	skeletal muscle
35	chr1:70675000-70686200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr1:70675400-70685800	Weak transcription	Primary hematopoietic stem cells	blood
37	chr1:70675400-70686400	Weak transcription	Osteobl	bone
38	chr1:70676000-70686400	Weak transcription	Brain Germinal Matrix	brain
39	chr1:70676200-70681600	Weak transcription	Stomach Smooth Muscle	stomach
40	chr1:70676200-70686400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
41	chr1:70676400-70686200	Weak transcription	Pancreas	Pancrea
42	chr1:70676400-70686200	Weak transcription	Psoas Muscle	Psoas
43	chr1:70676400-70686200	Weak transcription	Spleen	Spleen
44	chr1:70676400-70686600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
45	chr1:70676400-70686600	Weak transcription	NHDF-Ad	bronchial
46	chr1:70676400-70686600	Weak transcription	NHLF	lung
47	chr1:70676400-70686800	Weak transcription	Ovary	ovary
48	chr1:70677400-70681800	Weak transcription	Hela-S3	cervix
49	chr1:70677400-70682800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr1:70677800-70683200	Strong transcription	Primary T helper cells PMA-I stimulated	--

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