Variant report

Variant	nsv891429
Chromosome Location	chr8:125163219-125246937
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1202)
CpG islands
(count:427)
Chromatin interactive
region (count:118)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1202 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:125210094-125210406	K562	blood:	n/a	n/a
2	ARID3A	chr8:125245106-125245216	HepG2	liver:	n/a	n/a
3	ATF1	chr8:125241165-125241453	K562	blood:	n/a	n/a
4	ATF1	chr8:125210092-125210565	K562	blood:	n/a	n/a
5	ATF2	chr8:125208216-125208630	GM12878	blood:	n/a	n/a
6	ATF2	chr8:125208140-125208813	GM12878	blood:	n/a	n/a
7	ATF3	chr8:125212107-125213007	A549	lung:	n/a	n/a
8	ATF3	chr8:125238447-125238637	K562	blood:	n/a	n/a
9	ATF3	chr8:125241058-125241511	K562	blood:	n/a	n/a
10	ATF3	chr8:125212356-125212668	K562	blood:	n/a	n/a
11	ATF3	chr8:125212339-125213113	A549	lung:	n/a	n/a
12	ATF3	chr8:125209078-125209320	K562	blood:	n/a	n/a
13	BACH1	chr8:125174944-125174964	K562	blood:	n/a	n/a
14	BACH1	chr8:125212474-125212589	H1-hESC	embryonic stem cell:	n/a	n/a
15	BCL11A	chr8:125208252-125208936	GM12878	blood:	n/a	n/a
16	BCL3	chr8:125212119-125212897	A549	lung:	n/a	chr8:125212304-125212313
17	BCL3	chr8:125208486-125208970	GM12878	blood:	n/a	n/a
18	BCL3	chr8:125208544-125208913	GM12878	blood:	n/a	n/a
19	BCL3	chr8:125212003-125212840	A549	lung:	n/a	chr8:125212304-125212313
20	BCLAF1	chr8:125208378-125208959	GM12878	blood:	n/a	n/a
21	BCLAF1	chr8:125209926-125210664	GM12878	blood:	n/a	chr8:125210425-125210434
22	BCLAF1	chr8:125208057-125208956	GM12878	blood:	n/a	n/a
23	BHLHE40	chr8:125209135-125209338	K562	blood:	n/a	n/a
24	BHLHE40	chr8:125241125-125241401	K562	blood:	n/a	n/a
25	BHLHE40	chr8:125212456-125212760	K562	blood:	n/a	n/a
26	BHLHE40	chr8:125172594-125172694	K562	blood:	n/a	chr8:125172655-125172668 chr8:125172656-125172665 chr8:125172657-125172666 chr8:125172657-125172666 chr8:125172651-125172672
27	BHLHE40	chr8:125209889-125210454	K562	blood:	n/a	n/a
28	BRCA1	chr8:125212017-125212936	Hela-S3	cervix:	n/a	n/a
29	BRCA1	chr8:125184079-125184280	HepG2	liver:	n/a	n/a
30	CBX3	chr8:125212243-125212947	K562	blood:	n/a	n/a
31	CBX3	chr8:125208702-125209781	K562	blood:	n/a	n/a
32	CBX3	chr8:125241001-125241498	K562	blood:	n/a	n/a
33	CBX3	chr8:125238915-125239277	K562	blood:	n/a	n/a
34	CBX3	chr8:125209939-125210976	K562	blood:	n/a	chr8:125210227-125210238
35	CBX3	chr8:125211919-125213145	HCT-116	colon:	n/a	n/a
36	CCNT2	chr8:125177766-125178007	K562	blood:	n/a	n/a
37	CEBPB	chr8:125188115-125188303	H1-hESC	embryonic stem cell:	n/a	chr8:125188212-125188223
38	CEBPB	chr8:125210076-125210438	K562	blood:	n/a	n/a
39	CEBPB	chr8:125193553-125194201	IMR90	lung:	n/a	n/a
40	CEBPB	chr8:125218423-125218651	A549	lung:	n/a	n/a
41	CEBPB	chr8:125211988-125212842	ECC-1	luminal epithelium:	n/a	chr8:125212096-125212104
42	CEBPB	chr8:125218444-125218554	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr8:125241110-125241534	MCF-7	breast:	n/a	n/a
44	CEBPB	chr8:125245040-125245107	HepG2	liver:	n/a	chr8:125245068-125245079
45	CEBPB	chr8:125193572-125194178	ECC-1	luminal epithelium:	n/a	n/a
46	CEBPB	chr8:125229482-125229684	A549	lung:	n/a	chr8:125229576-125229589 chr8:125229578-125229589 chr8:125229576-125229587 chr8:125229578-125229587
47	CEBPB	chr8:125235517-125235766	A549	lung:	n/a	chr8:125235574-125235587 chr8:125235657-125235668
48	CEBPB	chr8:125211988-125213104	Hela-S3	cervix:	n/a	chr8:125212096-125212104
49	CEBPB	chr8:125239878-125241585	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr8:125218475-125218646	HepG2	liver:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:125183776-125183826	HL-60	blood:	n/a
2	chr8:125213448-125213498	SKMC	muscle:	n/a
3	chr8:125193955-125194005	PFSK-1	brain:	n/a
4	chr8:125193955-125194005	HCPEpiC	choroid plexus:	n/a
5	chr8:125239977-125240027	CMK	blood:	n/a
6	chr8:125239977-125240027	PANC-1	pancreas:	n/a
7	chr8:125239977-125240027	HUVEC	blood vessel:	n/a
8	chr8:125183790-125183840	SK-N-MC	brain:	n/a
9	chr8:125183758-125183808	HIPEpiC	eye:	n/a
10	chr8:125239977-125240027	IMR90	lung:	fetal
11	chr8:125183776-125183826	Jurkat	blood:	n/a
12	chr8:125183988-125184038	Hela-S3	cervix:	n/a
13	chr8:125183758-125183808	LNCaP	prostate:	n/a
14	chr8:125183758-125183808	AG10803	skin:	n/a
15	chr8:125193955-125194005	SK-N-SH_RA	brain:	n/a
16	chr8:125239977-125240027	HCF	heart:	n/a
17	chr8:125239977-125240027	SK-N-SH_RA	brain:	n/a
18	chr8:125183776-125183826	SK-N-SH	brain:	n/a
19	chr8:125193955-125194005	SK-N-SH	brain:	n/a
20	chr8:125183988-125184038	HCF	heart:	n/a
21	chr8:125183776-125183826	HCM	heart:	n/a
22	chr8:125183988-125184038	MCF-7	breast:	n/a
23	chr8:125183988-125184038	PrEC	prostate:	n/a
24	chr8:125213448-125213498	K562	blood:	n/a
25	chr8:125183758-125183808	HEK293	kidney:	embryo
26	chr8:125239977-125240027	GM12892	blood:	n/a
27	chr8:125183790-125183840	HRPEpiC	eye:	n/a
28	chr8:125183988-125184038	SKMC	muscle:	n/a
29	chr8:125183776-125183826	NH-A	brain:	n/a
30	chr8:125193955-125194005	HEEpiC	esophagus:	n/a
31	chr8:125183758-125183808	BJ	skin:	n/a
32	chr8:125183790-125183840	SK-N-SH_RA	brain:	n/a
33	chr8:125213448-125213498	NHDF-neo	bronchial:	n/a
34	chr8:125213448-125213498	A549	lung:	n/a
35	chr8:125183988-125184038	K562	blood:	n/a
36	chr8:125183790-125183840	ProgFib	skin:	n/a
37	chr8:125183776-125183826	AG09309	skin:	n/a
38	chr8:125213448-125213498	HCT-116	colon:	n/a
39	chr8:125193955-125194005	NT2-D1	testis:	n/a
40	chr8:125183758-125183808	HMEC	breast:	n/a
41	chr8:125183988-125184038	GM12891	blood:	n/a
42	chr8:125183776-125183826	AG10803	skin:	n/a
43	chr8:125183790-125183840	PFSK-1	brain:	n/a
44	chr8:125183776-125183826	ECC-1	luminal epithelium:	n/a
45	chr8:125239977-125240027	HNPCEpiC	eye:	n/a
46	chr8:125239977-125240027	HEEpiC	esophagus:	n/a
47	chr8:125213448-125213498	HMEC	breast:	n/a
48	chr8:125213448-125213498	HCF	heart:	n/a
49	chr8:125213448-125213498	AoSMC	blood vessel:	n/a
50	chr8:125183776-125183826	HIPEpiC	eye:	n/a

(count:118 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr8:125245505..125247774-chr8:125248974..125251123,2	K562	blood:
2	chr8:125187083..125190615-chr8:125190919..125193331,4	MCF-7	breast:
3	chr8:125168785..125170511-chr8:125190610..125193215,2	MCF-7	breast:
4	chr8:125166041..125167636-chr8:125188285..125189918,2	MCF-7	breast:
5	chr8:125148286..125150291-chr8:125179421..125181348,2	K562	blood:
6	chr8:125212409..125214102-chr8:125244609..125246382,2	MCF-7	breast:
7	chr8:125158434..125162428-chr8:125172218..125174995,4	MCF-7	breast:
8	chr8:125050107..125050678-chr8:125186177..125186793,3	MCF-7	breast:
9	chr8:125175881..125178146-chr8:125178944..125180876,2	K562	blood:
10	chr8:125159111..125160686-chr8:125174185..125175768,2	K562	blood:
11	chr8:125208077..125210980-chr8:125384559..125386358,2	K562	blood:
12	chr8:125228599..125231318-chr8:125233907..125235802,2	MCF-7	breast:
13	chr8:125206026..125208794-chr8:125210162..125212251,3	MCF-7	breast:
14	chr8:125214674..125216919-chr8:125220846..125223864,3	MCF-7	breast:
15	chr8:125191744..125194449-chr8:125391340..125393349,2	MCF-7	breast:
16	chr8:124780841..124782368-chr8:125233393..125235216,2	K562	blood:
17	chr8:125210719..125213522-chr8:125217440..125219569,3	K562	blood:
18	chr8:125159144..125163463-chr8:125165911..125169919,5	MCF-7	breast:
19	chr8:125208503..125210106-chr8:125213330..125215003,2	K562	blood:
20	chr8:125211433..125214005-chr8:125215089..125216813,2	MCF-7	breast:
21	chr8:125246490..125248480-chr8:125259051..125260941,2	K562	blood:
22	chr8:125050434..125051321-chr8:125181614..125182275,2	MCF-7	breast:
23	chr8:125168785..125170511-chr8:125190610..125193215,2	MCF-7	breast:
24	chr8:125241469..125243738-chr8:125246607..125249023,2	MCF-7	breast:
25	chr8:125243793..125245984-chr8:125248788..125251371,2	K562	blood:
26	chr8:125208503..125210106-chr8:125213330..125215003,2	K562	blood:
27	chr8:125212588..125215990-chr8:125362115..125365671,3	MCF-7	breast:
28	chr8:125201433..125203179-chr8:125210038..125211818,2	MCF-7	breast:
29	chr8:125201433..125203179-chr8:125210038..125211818,2	MCF-7	breast:
30	chr8:124936586..124937490-chr8:125244653..125245170,2	K562	blood:
31	chr8:125211433..125214005-chr8:125215089..125216813,2	MCF-7	breast:
32	chr8:125121321..125123454-chr8:125196535..125198369,2	MCF-7	breast:
33	chr8:125197907..125200093-chr8:125207154..125210134,2	K562	blood:
34	chr8:125121826..125124569-chr8:125246150..125248278,2	K562	blood:
35	chr8:125166041..125167636-chr8:125188285..125189918,2	MCF-7	breast:
36	chr8:125199649..125202361-chr8:125208886..125211211,2	K562	blood:
37	chr8:125050056..125052985-chr8:125210899..125215246,3	MCF-7	breast:
38	chr8:125175502..125179213-chr8:125180574..125185352,5	MCF-7	breast:
39	chr8:125049687..125050407-chr8:125194679..125195202,2	MCF-7	breast:
40	chr8:125162472..125164935-chr8:125272607..125274873,2	MCF-7	breast:
41	chr8:125245132..125247965-chr8:125248444..125250109,2	MCF-7	breast:
42	chr8:125210618..125213409-chr8:125383180..125386049,4	MCF-7	breast:
43	chr8:125181108..125183361-chr8:125183999..125186422,2	MCF-7	breast:
44	chr8:125237773..125239778-chr8:125383805..125385472,2	MCF-7	breast:
45	chr8:125177024..125178652-chr8:125180732..125182242,2	MCF-7	breast:
46	chr8:125052750..125054296-chr8:125209994..125212919,2	MCF-7	breast:
47	chr8:125197907..125200093-chr8:125207154..125210134,2	K562	blood:
48	chr8:125192128..125194093-chr8:125383543..125386541,2	MCF-7	breast:
49	chr8:125175881..125178146-chr8:125178944..125180876,2	K562	blood:
50	chr8:125222612..125225526-chr8:125239750..125242357,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMEM65-1	chr8:125220357-125220562	ENSG00000214803
2	lnc-TMEM65-1	chr8:125220357-125220364	XLOC_007205
3	lnc-TMEM65-1	chr8:125205393-125205785	XLOC_007205
4	lnc-TMEM65-1	chr8:125204912-125205785	ENSG00000214803

No data

Variant related genes	Relation type
ARF1P3	TF binding region
FER1L6-AS2	TF binding region
ARF1P3	CpG island
FER1L6-AS2	CpG island
ENSG00000253868	chromatin interactions
ENSG00000176853	chromatin interactions
ENSG00000144802	chromatin interactions
ENSG00000164983	chromatin interactions
ENSG00000181171	chromatin interactions
ENSG00000214803	chromatin interactions
ENSG00000253227	chromatin interactions
ENSG00000250727	chromatin interactions
ENSG00000254249	chromatin interactions
ENSG00000206724	chromatin interactions
FAM117B	miRNA target sites
PSPH	miRNA target sites

Extended variants
information (count: 3205 )
Associated
traits (count: 142 )

Variant overlapped rSNPs/rCNVs (count:3205 , 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	rs6986229	chr8:125163219-125163220	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs11784687	chr8:125163241-125163242	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs371661215	chr8:125163337-125163338	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs35293410	chr8:125163398-125163399	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs370087797	chr8:125163399-125163400	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs367986921	chr8:125163405-125163406	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs527485182	chr8:125163433-125163434	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs376705915	chr8:125163436-125163437	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs547573106	chr8:125163447-125163448	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs80059034	chr8:125163453-125163454	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs35000230	chr8:125163516-125163517	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs139558147	chr8:125163547-125163548	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs569665581	chr8:125163586-125163587	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs141884262	chr8:125163587-125163588	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs559209134	chr8:125163593-125163594	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs572365417	chr8:125163613-125163614	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs7818609	chr8:125163655-125163656	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs376915247	chr8:125163656-125163657	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs558157288	chr8:125163676-125163677	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs186818960	chr8:125163682-125163683	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs574670658	chr8:125163691-125163692	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs150648413	chr8:125163703-125163704	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs192406218	chr8:125163714-125163715	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs563620839	chr8:125163721-125163722	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs532584299	chr8:125163725-125163726	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs545831258	chr8:125163774-125163775	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs184034806	chr8:125163793-125163794	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs139554564	chr8:125163810-125163811	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs74568851	chr8:125163830-125163831	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs149723159	chr8:125163844-125163845	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs116969208	chr8:125163860-125163861	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs549897802	chr8:125163894-125163895	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs35027280	chr8:125163935-125163936	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs569605675	chr8:125163975-125163976	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs57354698	chr8:125164092-125164093	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs542925663	chr8:125164093-125164094	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs189110516	chr8:125164152-125164153	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs569776387	chr8:125164158-125164159	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs535013974	chr8:125164182-125164183	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs554827877	chr8:125164238-125164239	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs574733200	chr8:125164255-125164256	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs543651400	chr8:125164256-125164257	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs192843867	chr8:125164257-125164258	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs577226560	chr8:125164284-125164285	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs546193866	chr8:125164299-125164300	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs139771563	chr8:125164312-125164313	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs573250879	chr8:125164318-125164319	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs541369188	chr8:125164320-125164321	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs561154563	chr8:125164331-125164332	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs4871466	chr8:125164336-125164337	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:142)

Disease	PMID	Source
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
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	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	17603634	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	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
Acute myeloid leukemia	20729466	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
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	20932292	CNVD
Gastric cancer	22539939	CNVD
Breast cancer	22056952	CNVD
Langer-Giedion syndrome	16773131	CNVD
Lung cancer	16740712	CNVD
Mental retardation	16773131	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Langer-Giedion syndrome	22470819	CNVD
Cornelia de Lange syndrome	24599119	CNVD
Gastric cancer	21528007	CNVD
Breast cancer	22532251	CNVD
Cervical cancer	21062161	CNVD
Cancer	21129771	CNVD
benign familial neonatal convulsions	18472482	CNVD
Breast cancer	16417655	CNVD
Astrocytoma	17387387	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	20814816	CNVD
Colorectal cancer	22486879	CNVD
Breast cancer	17908964	CNVD
Colorectal cancer	20031965	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian cancer	17908964	CNVD
Ovarian cancer	20031965	CNVD
Prostate cancer	20031965	CNVD
Non-small cell lung cancer	17643093	CNVD
Prostate cancer	19242612	CNVD
Colorectal cancer	16774939	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	18628472	CNVD
Malignant melanoma	17260012	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	16397240	CNVD
Multiple myeloma	16461302	CNVD
Multiple myeloma	16616336	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Breast cancer	21364760	CNVD
Burkitt''s lymphoma	20823134	CNVD
Colorectal cancer	21645411	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute myeloid leukemia	18379011	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Breast cancer	21611746	CNVD
Ductal carcinoma	22052326	CNVD
Gastric cancer	18160780	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1032 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:125150400-125165600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr8:125154200-125165600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr8:125158200-125165800	Weak transcription	Spleen	Spleen
4	chr8:125160400-125165600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr8:125160400-125165600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr8:125164200-125164400	Enhancers	Lung	lung
7	chr8:125165600-125165800	Enhancers	Esophagus	oesophagus
8	chr8:125165600-125166000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr8:125165600-125166000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr8:125165600-125166400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr8:125165600-125166400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr8:125165800-125166000	Enhancers	Spleen	Spleen
13	chr8:125171000-125171600	Enhancers	Duodenum Mucosa	Duodenum
14	chr8:125171000-125171800	Enhancers	Pancreas	Pancrea
15	chr8:125171000-125172400	Enhancers	Fetal Intestine Large	intestine
16	chr8:125171000-125172400	Enhancers	Fetal Intestine Small	intestine
17	chr8:125171400-125172600	Enhancers	Fetal Heart	heart
18	chr8:125171600-125172000	Enhancers	Stomach Mucosa	stomach
19	chr8:125172400-125177400	Weak transcription	Fetal Intestine Large	intestine
20	chr8:125172600-125172800	Enhancers	Brain Germinal Matrix	brain
21	chr8:125172800-125175200	Weak transcription	Brain Germinal Matrix	brain
22	chr8:125174400-125175000	Enhancers	Aorta	Aorta
23	chr8:125174800-125175200	Enhancers	Gastric	stomach
24	chr8:125174800-125175400	Enhancers	K562	blood
25	chr8:125174800-125175800	Enhancers	Brain Angular Gyrus	brain
26	chr8:125174800-125177000	Enhancers	Fetal Brain Male	brain
27	chr8:125174800-125177200	Enhancers	Fetal Brain Female	brain
28	chr8:125175000-125177400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr8:125175200-125176800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr8:125175200-125176800	Weak transcription	Gastric	stomach
31	chr8:125175200-125177000	Enhancers	Brain Germinal Matrix	brain
32	chr8:125175200-125177200	Enhancers	Cortex derived primary cultured neurospheres	brain
33	chr8:125175400-125184000	Weak transcription	K562	blood
34	chr8:125175600-125176600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr8:125176600-125182000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr8:125176800-125177000	Enhancers	Gastric	stomach
37	chr8:125177000-125180200	Weak transcription	Fetal Brain Male	brain
38	chr8:125177400-125179000	Enhancers	Fetal Intestine Large	intestine
39	chr8:125177400-125179200	Enhancers	Fetal Intestine Small	intestine
40	chr8:125177800-125178400	Enhancers	Pancreatic Islets	Pancreatic Islet
41	chr8:125178400-125184000	Weak transcription	Pancreatic Islets	Pancreatic Islet
42	chr8:125178600-125178800	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr8:125178600-125179400	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr8:125178800-125179000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr8:125179000-125179200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr8:125179200-125184000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
47	chr8:125180000-125180800	Enhancers	Fetal Heart	heart
48	chr8:125180000-125181400	Enhancers	Left Ventricle	heart
49	chr8:125180200-125180600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr8:125180200-125180600	Enhancers	Fetal Brain Male	brain

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