Variant report

Variant	nsv1018510
Chromosome Location	chr8:110403496-110504029
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:641)
CpG islands
(count:183)
Chromatin interactive
region (count:129)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:641 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:110423847-110424726	K562	blood:	n/a	n/a
2	ARID3A	chr8:110404919-110405551	K562	blood:	n/a	n/a
3	ARID3A	chr8:110411923-110412202	K562	blood:	n/a	n/a
4	ARID3A	chr8:110440493-110441166	K562	blood:	n/a	n/a
5	ATF1	chr8:110473883-110474077	K562	blood:	n/a	n/a
6	ATF1	chr8:110440707-110441089	K562	blood:	n/a	n/a
7	ATF1	chr8:110423878-110424292	K562	blood:	n/a	n/a
8	BACH1	chr8:110477232-110477389	K562	blood:	n/a	n/a
9	BACH1	chr8:110403534-110403559	K562	blood:	n/a	n/a
10	BACH1	chr8:110440421-110441061	K562	blood:	n/a	n/a
11	BACH1	chr8:110405000-110405477	K562	blood:	n/a	n/a
12	BCL3	chr8:110461550-110461755	GM12878	blood:	n/a	n/a
13	BCL3	chr8:110461556-110461800	GM12878	blood:	n/a	n/a
14	BCL3	chr8:110405674-110405957	GM12878	blood:	n/a	n/a
15	BCL3	chr8:110414649-110414919	GM12878	blood:	n/a	n/a
16	BCL3	chr8:110458697-110459000	GM12878	blood:	n/a	n/a
17	BHLHE40	chr8:110463120-110463463	K562	blood:	n/a	n/a
18	BHLHE40	chr8:110405685-110405960	K562	blood:	n/a	n/a
19	BHLHE40	chr8:110440560-110441059	K562	blood:	n/a	n/a
20	BHLHE40	chr8:110477349-110477423	K562	blood:	n/a	n/a
21	BHLHE40	chr8:110423807-110424663	K562	blood:	n/a	n/a
22	BRCA1	chr8:110463243-110463494	HepG2	liver:	n/a	n/a
23	CBX3	chr8:110423576-110424294	K562	blood:	n/a	n/a
24	CBX3	chr8:110463124-110463539	K562	blood:	n/a	n/a
25	CBX3	chr8:110430371-110430686	K562	blood:	n/a	n/a
26	CBX3	chr8:110440551-110441149	K562	blood:	n/a	n/a
27	CBX3	chr8:110440772-110441112	K562	blood:	n/a	n/a
28	CBX3	chr8:110430348-110430767	K562	blood:	n/a	n/a
29	CBX3	chr8:110463004-110463661	HCT-116	colon:	n/a	n/a
30	CCNT2	chr8:110423981-110424270	K562	blood:	n/a	n/a
31	CCNT2	chr8:110404892-110405465	K562	blood:	n/a	n/a
32	CCNT2	chr8:110477620-110477848	K562	blood:	n/a	n/a
33	CCNT2	chr8:110442112-110442392	K562	blood:	n/a	chr8:110442292-110442312
34	CCNT2	chr8:110440658-110441093	K562	blood:	n/a	n/a
35	CEBPB	chr8:110422046-110422267	K562	blood:	n/a	chr8:110422165-110422176
36	CEBPB	chr8:110425298-110425665	K562	blood:	n/a	n/a
37	CEBPB	chr8:110489630-110489818	A549	lung:	n/a	chr8:110489716-110489727
38	CEBPB	chr8:110404944-110405322	K562	blood:	n/a	n/a
39	CEBPB	chr8:110421053-110421296	MCF-7	breast:	n/a	n/a
40	CEBPB	chr8:110411769-110412064	A549	lung:	n/a	chr8:110411939-110411952
41	CEBPB	chr8:110421134-110421323	K562	blood:	n/a	n/a
42	CEBPB	chr8:110461558-110461826	A549	lung:	n/a	n/a
43	CEBPB	chr8:110411745-110412260	K562	blood:	n/a	chr8:110411939-110411952
44	CEBPB	chr8:110425348-110425629	A549	lung:	n/a	n/a
45	CEBPB	chr8:110430341-110430561	HepG2	liver:	n/a	chr8:110430419-110430430 chr8:110430419-110430432 chr8:110430421-110430432
46	CEBPB	chr8:110407949-110408209	K562	blood:	n/a	n/a
47	CEBPB	chr8:110453429-110453629	K562	blood:	n/a	n/a
48	CEBPB	chr8:110440612-110441055	K562	blood:	n/a	chr8:110440743-110440756 chr8:110441035-110441046 chr8:110440743-110440754
49	CEBPB	chr8:110464592-110464860	HepG2	liver:	n/a	chr8:110464748-110464759
50	CEBPB	chr8:110477662-110477973	K562	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:110456058-110456108	GM19239	blood:	n/a
2	chr8:110497696-110497746	NHDF-neo	bronchial:	n/a
3	chr8:110497696-110497746	SAEC	small airway:	n/a
4	chr8:110497696-110497746	ECC-1	luminal epithelium:	n/a
5	chr8:110497696-110497746	HCF	heart:	n/a
6	chr8:110470148-110470198	U87	brain:	n/a
7	chr8:110470148-110470198	HCT-116	colon:	n/a
8	chr8:110470148-110470198	MCF-7	breast:	n/a
9	chr8:110497696-110497746	GM12878	blood:	n/a
10	chr8:110456058-110456108	HCPEpiC	choroid plexus:	n/a
11	chr8:110456058-110456108	HRCEpiC	kidney:	n/a
12	chr8:110470148-110470198	Jurkat	blood:	n/a
13	chr8:110470148-110470198	H1-hESC	embryonic stem cell:	embryo
14	chr8:110497696-110497746	NH-A	brain:	n/a
15	chr8:110470148-110470198	Hepatocyte	liver:	n/a
16	chr8:110470148-110470198	K562	blood:	n/a
17	chr8:110456058-110456108	GM12878	blood:	n/a
18	chr8:110497696-110497746	Hela-S3	cervix:	n/a
19	chr8:110497696-110497746	SKMC	muscle:	n/a
20	chr8:110456058-110456108	Hepatocyte	liver:	n/a
21	chr8:110497696-110497746	HNPCEpiC	eye:	n/a
22	chr8:110497696-110497746	HRE	kidney:	n/a
23	chr8:110497696-110497746	BE2_C	brain:	n/a
24	chr8:110456058-110456108	HIPEpiC	eye:	n/a
25	chr8:110456058-110456108	HCT-116	colon:	n/a
26	chr8:110456058-110456108	HMEC	breast:	n/a
27	chr8:110470148-110470198	NHDF-neo	bronchial:	n/a
28	chr8:110456058-110456108	HL-60	blood:	n/a
29	chr8:110456058-110456108	MCF10A-Er-Src	breast:	n/a
30	chr8:110470148-110470198	SK-N-SH_RA	brain:	n/a
31	chr8:110497696-110497746	BJ	skin:	n/a
32	chr8:110470148-110470198	GM12892	blood:	n/a
33	chr8:110470148-110470198	SAEC	small airway:	n/a
34	chr8:110497696-110497746	MCF10A-Er-Src	breast:	n/a
35	chr8:110497696-110497746	NT2-D1	testis:	n/a
36	chr8:110456058-110456108	U87	brain:	n/a
37	chr8:110456058-110456108	AoSMC	blood vessel:	n/a
38	chr8:110497696-110497746	T-47D	breast:	n/a
39	chr8:110470148-110470198	Hela-S3	cervix:	n/a
40	chr8:110497696-110497746	AoSMC	blood vessel:	n/a
41	chr8:110497696-110497746	GM12891	blood:	n/a
42	chr8:110497696-110497746	HAEpiC	amniotic membrane:	n/a
43	chr8:110470148-110470198	NH-A	brain:	n/a
44	chr8:110456058-110456108	ECC-1	luminal epithelium:	n/a
45	chr8:110497696-110497746	HUVEC	blood vessel:	n/a
46	chr8:110497696-110497746	HEK293	kidney:	embryo
47	chr8:110456058-110456108	GM12891	blood:	n/a
48	chr8:110497696-110497746	RPTEC	kidney:	n/a
49	chr8:110470148-110470198	HIPEpiC	eye:	n/a
50	chr8:110470148-110470198	LNCaP	prostate:	n/a

(count:129 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr8:110429297..110431956-chr8:110445022..110447169,2	K562	blood:
2	chr8:110463281..110463836-chr8:110732082..110732942,2	MCF-7	breast:
3	chr8:110434476..110437151-chr8:110440574..110442401,2	K562	blood:
4	chr8:110480733..110484366-chr8:110549857..110553138,3	MCF-7	breast:
5	chr8:110418593..110421354-chr8:110426725..110428421,2	K562	blood:
6	chr8:110403199..110405955-chr8:110549557..110552285,2	K562	blood:
7	chr8:110441796..110443720-chr8:110443789..110445580,2	K562	blood:
8	chr8:110418895..110420648-chr8:110550945..110553899,2	MCF-7	breast:
9	chr8:110425956..110428666-chr8:110434429..110437325,2	K562	blood:
10	chr8:110461291..110465454-chr8:110550197..110554392,6	MCF-7	breast:
11	chr8:110418172..110419815-chr8:110421960..110424604,2	K562	blood:
12	chr8:110397526..110401680-chr8:110402055..110405525,5	K562	blood:
13	chr8:110401286..110403150-chr8:110410223..110413005,2	MCF-7	breast:
14	chr8:110431847..110433717-chr8:110434845..110437578,2	K562	blood:
15	chr8:110466327..110471648-chr8:110473148..110480342,6	K562	blood:
16	chr8:110373263..110375819-chr8:110436169..110438487,2	K562	blood:
17	chr8:110462548..110464182-chr8:110467144..110470132,2	MCF-7	breast:
18	chr8:110466327..110471648-chr8:110473148..110480342,6	K562	blood:
19	chr8:110403524..110405569-chr8:110405749..110408596,2	K562	blood:
20	chr8:110462238..110464562-chr8:110469589..110471882,2	K562	blood:
21	chr8:110462782..110463819-chr8:110664356..110665380,8	MCF-7	breast:
22	chr8:110450010..110452519-chr8:110455545..110457090,2	K562	blood:
23	chr8:110462866..110463874-chr8:110563606..110564958,17	MCF-7	breast:
24	chr8:110463291..110463825-chr8:110573423..110574203,2	MCF-7	breast:
25	chr8:110443668..110447226-chr8:110448028..110451170,4	K562	blood:
26	chr8:110470771..110473127-chr8:110474379..110476056,2	MCF-7	breast:
27	chr8:110443668..110445641-chr8:110448319..110451170,3	K562	blood:
28	chr8:110450010..110452519-chr8:110455545..110457090,2	K562	blood:
29	chr8:110438163..110441059-chr8:110444438..110447388,2	K562	blood:
30	chr8:110483309..110485365-chr8:110487237..110489170,2	MCF-7	breast:
31	chr8:110462528..110463405-chr8:110651980..110652480,2	MCF-7	breast:
32	chr8:110463988..110464714-chr8:110664335..110664899,2	MCF-7	breast:
33	chr8:110500097..110503001-chr8:110504877..110506686,2	MCF-7	breast:
34	chr8:110414719..110417184-chr8:110648514..110651300,2	MCF-7	breast:
35	chr8:110459151..110460064-chr8:110664745..110665328,2	MCF-7	breast:
36	chr8:110438163..110441059-chr8:110444438..110447388,2	K562	blood:
37	chr8:110470771..110473127-chr8:110474379..110476056,2	MCF-7	breast:
38	chr8:110476428..110479434-chr8:110485234..110488569,3	MCF-7	breast:
39	chr8:110477232..110479716-chr8:110551976..110554277,3	MCF-7	breast:
40	chr8:110490813..110493110-chr8:110549363..110552380,3	MCF-7	breast:
41	chr8:110455738..110458666-chr8:110463282..110464812,2	MCF-7	breast:
42	chr8:110485934..110489021-chr8:110489156..110492335,3	MCF-7	breast:
43	chr8:110487318..110489249-chr8:110492747..110497686,4	MCF-7	breast:
44	chr8:110483442..110487678-chr8:110550408..110553451,5	MCF-7	breast:
45	chr8:110374980..110376608-chr8:110402670..110404308,2	K562	blood:
46	chr8:110411451..110413359-chr8:110418061..110419801,2	K562	blood:
47	chr8:110484343..110486206-chr8:110487564..110489651,2	K562	blood:
48	chr8:110403354..110405591-chr8:110412229..110414153,2	K562	blood:
49	chr8:110429688..110434092-chr8:110438385..110444037,5	K562	blood:
50	chr8:110462889..110463619-chr8:110656542..110657170,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000254185	TF binding region
PKHD1L1	TF binding region
ENSG00000254185	CpG island
PKHD1L1	CpG island
ENSG00000205038	chromatin interactions
ENSG00000147642	chromatin interactions
ENSG00000147654	chromatin interactions
ENSG00000120533	chromatin interactions
ENSG00000248050	chromatin interactions
ENSG00000120526	chromatin interactions

Extended variants
information (count: 3236 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:3236 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13278812	chr8:110403496-110403497	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs560505377	chr8:110403516-110403517	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs376100863	chr8:110403538-110403539	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs561489032	chr8:110403568-110403569	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs368559877	chr8:110403680-110403681	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs547241756	chr8:110403684-110403685	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs1379370	chr8:110403698-110403699	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs145107867	chr8:110403720-110403721	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs528014723	chr8:110403757-110403758	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs569370846	chr8:110403799-110403800	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs571239240	chr8:110403801-110403802	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs538297011	chr8:110403821-110403822	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs554781354	chr8:110403834-110403835	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs567428037	chr8:110403839-110403840	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs536086154	chr8:110403893-110403894	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs547645004	chr8:110403904-110403905	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs192110862	chr8:110403906-110403907	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs540053714	chr8:110403926-110403927	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs182153038	chr8:110403932-110403933	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs558080885	chr8:110403952-110403953	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs138921994	chr8:110403968-110403969	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs544259361	chr8:110403989-110403990	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs142154822	chr8:110403991-110403992	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs186037487	chr8:110404000-110404001	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs376612897	chr8:110404004-110404005	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs560757927	chr8:110404048-110404049	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs190955920	chr8:110404070-110404071	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs182447262	chr8:110404107-110404108	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs187144499	chr8:110404119-110404120	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs531631966	chr8:110404178-110404179	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs536311468	chr8:110404179-110404180	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs556296044	chr8:110404208-110404209	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs568497631	chr8:110404259-110404260	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs536439243	chr8:110404279-110404280	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs569813051	chr8:110404316-110404317	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs7834361	chr8:110404333-110404334	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs538501990	chr8:110404378-110404379	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs190163071	chr8:110404402-110404403	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs146140556	chr8:110404418-110404419	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs575146852	chr8:110404431-110404432	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs537469424	chr8:110404440-110404441	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs368753868	chr8:110404441-110404442	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs182783234	chr8:110404492-110404493	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs188389808	chr8:110404558-110404559	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs150842865	chr8:110404576-110404577	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs563781368	chr8:110404577-110404578	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs138232529	chr8:110404585-110404586	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs62508076	chr8:110404635-110404636	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs532502733	chr8:110404682-110404683	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs193244443	chr8:110404704-110404705	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:104)

Disease	PMID	Source
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Multiple myeloma	16461302	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Gastric cancer	22539939	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	21645411	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Gastric cancer	22014070	CNVD
Ovarian cancer	21781307	CNVD

Chromatin state (count:144 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:110402200-110403600	Weak transcription	K562	blood
2	chr8:110402600-110404400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr8:110403600-110403800	Enhancers	Brain Germinal Matrix	brain
4	chr8:110403600-110404200	Enhancers	K562	blood
5	chr8:110404000-110405000	Weak transcription	Brain Germinal Matrix	brain
6	chr8:110404200-110405000	Weak transcription	K562	blood
7	chr8:110404400-110404600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr8:110404600-110405000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr8:110405000-110405600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr8:110405000-110405800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr8:110405000-110405800	Enhancers	Brain Germinal Matrix	brain
12	chr8:110405000-110406000	Enhancers	K562	blood
13	chr8:110405800-110406800	Weak transcription	Brain Germinal Matrix	brain
14	chr8:110406000-110408600	Weak transcription	K562	blood
15	chr8:110407000-110407200	Enhancers	Brain Germinal Matrix	brain
16	chr8:110407000-110407400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr8:110408600-110409000	Enhancers	K562	blood
18	chr8:110409000-110409400	Enhancers	Primary neutrophils fromperipheralblood	blood
19	chr8:110409400-110414200	Weak transcription	Primary neutrophils fromperipheralblood	blood
20	chr8:110414200-110415800	Enhancers	Primary neutrophils fromperipheralblood	blood
21	chr8:110418800-110421600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr8:110419800-110421200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr8:110423600-110423800	Enhancers	K562	blood
24	chr8:110423600-110424600	Enhancers	HUVEC	blood vessel
25	chr8:110423800-110424200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr8:110423800-110424200	Flanking Active TSS	K562	blood
27	chr8:110423800-110424800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr8:110424000-110424600	Enhancers	Muscle Satellite Cultured Cells	--
29	chr8:110424200-110424400	Enhancers	A549	lung
30	chr8:110424200-110424400	Active TSS	K562	blood
31	chr8:110424200-110424600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr8:110424400-110424600	Flanking Active TSS	K562	blood
33	chr8:110424600-110424800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr8:110424600-110424800	Active TSS	K562	blood
35	chr8:110424800-110425800	Weak transcription	K562	blood
36	chr8:110425800-110426000	Enhancers	K562	blood
37	chr8:110427600-110428200	Enhancers	Fetal Intestine Small	intestine
38	chr8:110428200-110428600	Weak transcription	Fetal Intestine Small	intestine
39	chr8:110428600-110429200	Enhancers	Fetal Intestine Small	intestine
40	chr8:110430800-110431200	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr8:110430800-110431600	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr8:110434400-110435400	Active TSS	K562	blood
43	chr8:110436600-110437000	Enhancers	Stomach Mucosa	stomach
44	chr8:110440200-110440400	Enhancers	K562	blood
45	chr8:110440400-110440600	Flanking Active TSS	K562	blood
46	chr8:110440400-110440800	Enhancers	Primary neutrophils fromperipheralblood	blood
47	chr8:110440600-110440800	Enhancers	K562	blood
48	chr8:110440800-110441000	Flanking Active TSS	K562	blood
49	chr8:110440800-110441000	Enhancers	Monocytes-CD14+_RO01746	blood
50	chr8:110441000-110442800	Enhancers	K562	blood

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