Variant report

Variant	nsv611882
Chromosome Location	chr8:111342240-111722469
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1037)
CpG islands
(count:123)
Chromatin interactive
region (count:86)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1037 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:111370803-111370846	K562	blood:	n/a	n/a
2	BACH1	chr8:111523582-111523674	K562	blood:	n/a	n/a
3	BACH1	chr8:111719799-111719982	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr8:111361264-111361282	K562	blood:	n/a	n/a
5	BATF	chr8:111380515-111380775	GM12878	blood:	n/a	n/a
6	BATF	chr8:111380529-111380748	GM12878	blood:	n/a	n/a
7	BCL3	chr8:111719822-111720092	GM12878	blood:	n/a	n/a
8	CEBPB	chr8:111470033-111470437	MCF-7	breast:	n/a	n/a
9	CEBPB	chr8:111503758-111503941	H1-hESC	embryonic stem cell:	n/a	chr8:111503888-111503901 chr8:111503888-111503899 chr8:111503889-111503900 chr8:111503888-111503901 chr8:111503888-111503901 chr8:111503888-111503899
10	CEBPB	chr8:111539118-111539315	K562	blood:	n/a	chr8:111539185-111539196 chr8:111539167-111539178
11	CEBPB	chr8:111348693-111348897	A549	lung:	n/a	n/a
12	CEBPB	chr8:111539099-111539344	A549	lung:	n/a	chr8:111539185-111539196 chr8:111539167-111539178
13	CEBPB	chr8:111714073-111714166	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr8:111485138-111485350	HepG2	liver:	n/a	n/a
15	CEBPB	chr8:111655239-111655443	H1-hESC	embryonic stem cell:	n/a	chr8:111655308-111655319
16	CEBPB	chr8:111525002-111525202	HepG2	liver:	n/a	chr8:111525140-111525151 chr8:111525141-111525150 chr8:111525139-111525150
17	CEBPB	chr8:111617237-111617564	HepG2	liver:	n/a	chr8:111617393-111617404
18	CEBPB	chr8:111634949-111635197	IMR90	lung:	n/a	chr8:111635032-111635043
19	CEBPB	chr8:111539037-111539369	IMR90	lung:	n/a	chr8:111539185-111539196 chr8:111539167-111539178
20	CEBPB	chr8:111551859-111552317	MCF-7	breast:	n/a	n/a
21	CEBPB	chr8:111539090-111539260	H1-hESC	embryonic stem cell:	n/a	chr8:111539185-111539196 chr8:111539167-111539178
22	CEBPB	chr8:111407619-111407631	K562	blood:	n/a	n/a
23	CEBPB	chr8:111605973-111606139	HepG2	liver:	n/a	chr8:111606013-111606024
24	CEBPB	chr8:111623432-111623641	MCF-7	breast:	n/a	n/a
25	CEBPB	chr8:111470060-111470420	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr8:111580266-111580852	MCF-7	breast:	n/a	chr8:111580459-111580472
27	CEBPB	chr8:111407057-111407265	HepG2	liver:	n/a	chr8:111407125-111407136
28	CEBPB	chr8:111673382-111673531	HepG2	liver:	n/a	n/a
29	CEBPB	chr8:111563470-111564178	MCF-7	breast:	n/a	chr8:111563940-111563951
30	CEBPB	chr8:111505335-111505447	A549	lung:	n/a	chr8:111505347-111505358 chr8:111505411-111505422
31	CEBPB	chr8:111630967-111631208	HepG2	liver:	n/a	chr8:111631031-111631042
32	CEBPB	chr8:111684904-111685112	IMR90	lung:	n/a	n/a
33	CEBPB	chr8:111407564-111407694	HepG2	liver:	n/a	chr8:111407634-111407645
34	CEBPB	chr8:111503761-111504005	HepG2	liver:	n/a	chr8:111503888-111503901 chr8:111503888-111503899 chr8:111503889-111503900 chr8:111503888-111503901 chr8:111503888-111503901 chr8:111503888-111503899
35	CEBPB	chr8:111663882-111664226	IMR90	lung:	n/a	n/a
36	CEBPB	chr8:111634989-111635163	HepG2	liver:	n/a	chr8:111635032-111635043
37	CEBPB	chr8:111663840-111664346	MCF-7	breast:	n/a	n/a
38	CEBPB	chr8:111551759-111552363	MCF-7	breast:	n/a	n/a
39	CEBPB	chr8:111505352-111505461	HepG2	liver:	n/a	chr8:111505411-111505422
40	CEBPB	chr8:111563765-111564094	A549	lung:	n/a	chr8:111563940-111563951
41	CEBPB	chr8:111563777-111564088	HepG2	liver:	n/a	chr8:111563940-111563951
42	CEBPB	chr8:111485063-111485373	IMR90	lung:	n/a	n/a
43	CEBPB	chr8:111688373-111688402	K562	blood:	n/a	n/a
44	CEBPB	chr8:111599775-111599936	K562	blood:	n/a	chr8:111599861-111599872
45	CEBPB	chr8:111573269-111573432	A549	lung:	n/a	n/a
46	CEBPB	chr8:111392636-111392756	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr8:111539028-111539286	HepG2	liver:	n/a	chr8:111539185-111539196 chr8:111539167-111539178
48	CEBPB	chr8:111566321-111566477	A549	lung:	n/a	chr8:111566413-111566424
49	CEBPB	chr8:111678183-111678436	A549	lung:	n/a	chr8:111678273-111678284
50	CEBPB	chr8:111346863-111346939	HepG2	liver:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:111342449-111342499	HRE	kidney:	n/a
2	chr8:111342449-111342499	HRE	kidney:	n/a
3	chr8:111342449-111342499	BJ	skin:	n/a
4	chr8:111707758-111707808	HMEC	breast:	n/a
5	chr8:111707758-111707808	HCPEpiC	choroid plexus:	n/a
6	chr8:111707758-111707808	HIPEpiC	eye:	n/a
7	chr8:111342449-111342499	K562	blood:	n/a
8	chr8:111707758-111707808	HAEpiC	amniotic membrane:	n/a
9	chr8:111342449-111342499	GM19239	blood:	n/a
10	chr8:111342449-111342499	HCF	heart:	n/a
11	chr8:111342449-111342499	Caco-2	colon:	n/a
12	chr8:111342449-111342499	U87	brain:	n/a
13	chr8:111707758-111707808	HPAEpiC	pulmonary alveolar:	n/a
14	chr8:111342449-111342499	Jurkat	blood:	n/a
15	chr8:111342449-111342499	HepG2	liver:	n/a
16	chr8:111342449-111342499	CMK	blood:	n/a
17	chr8:111707758-111707808	Hela-S3	cervix:	n/a
18	chr8:111342449-111342499	MCF10A-Er-Src	breast:	n/a
19	chr8:111707758-111707808	A549	lung:	n/a
20	chr8:111707758-111707808	SAEC	small airway:	n/a
21	chr8:111707758-111707808	BJ	skin:	n/a
22	chr8:111707758-111707808	PFSK-1	brain:	n/a
23	chr8:111342449-111342499	HNPCEpiC	eye:	n/a
24	chr8:111707758-111707808	IMR90	lung:	fetal
25	chr8:111342449-111342499	HCPEpiC	choroid plexus:	n/a
26	chr8:111342449-111342499	HUVEC	blood vessel:	n/a
27	chr8:111342449-111342499	AG09309	skin:	n/a
28	chr8:111342449-111342499	NHDF-neo	bronchial:	n/a
29	chr8:111342449-111342499	PANC-1	pancreas:	n/a
30	chr8:111707758-111707808	NHBE	bronchial:	n/a
31	chr8:111342449-111342499	PrEC	prostate:	n/a
32	chr8:111342449-111342499	NHBE	bronchial:	n/a
33	chr8:111707758-111707808	HUVEC	blood vessel:	n/a
34	chr8:111342449-111342499	ProgFib	skin:	n/a
35	chr8:111707758-111707808	NHDF-neo	bronchial:	n/a
36	chr8:111707758-111707808	K562	blood:	n/a
37	chr8:111707758-111707808	AG04450	lung:	fetal
38	chr8:111707758-111707808	RPTEC	kidney:	n/a
39	chr8:111707758-111707808	GM19239	blood:	n/a
40	chr8:111707758-111707808	NB4	blood:	n/a
41	chr8:111342449-111342499	GM12878	blood:	n/a
42	chr8:111707758-111707808	SK-N-SH_RA	brain:	n/a
43	chr8:111342449-111342499	SAEC	small airway:	n/a
44	chr8:111707758-111707808	HCF	heart:	n/a
45	chr8:111342449-111342499	GM12891	blood:	n/a
46	chr8:111707758-111707808	HEK293	kidney:	embryo
47	chr8:111342449-111342499	NH-A	brain:	n/a
48	chr8:111707758-111707808	Jurkat	blood:	n/a
49	chr8:111707758-111707808	CMK	blood:	n/a
50	chr8:111707758-111707808	ovcar-3	ovarian:	n/a

(count:86 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:111563289..111565363-chr8:111579783..111581298,2	MCF-7	breast:
2	chr11:74302754..74304460-chr8:111676552..111678415,2	MCF-7	breast:
3	chr8:111579951..111580480-chr8:111668750..111669442,2	MCF-7	breast:
4	chr8:111444766..111447245-chr8:111451075..111453827,2	K562	blood:
5	chr8:111618584..111620243-chr8:111621032..111622618,2	MCF-7	breast:
6	chr8:111594065..111596990-chr8:111668768..111671358,2	MCF-7	breast:
7	chr8:111702766..111704836-chr8:111705809..111708776,2	MCF-7	breast:
8	chr8:111561274..111563938-chr8:111668171..111670064,2	MCF-7	breast:
9	chr8:111665338..111666843-chr8:111677219..111678888,2	K562	blood:
10	chr6:47444917..47447011-chr8:111717811..111719807,2	MCF-7	breast:
11	chr8:111551159..111553132-chr8:111554691..111557321,2	MCF-7	breast:
12	chr8:111689286..111692174-chr8:111701872..111704181,2	MCF-7	breast:
13	chr12:43241796..43242729-chr8:111709968..111710717,2	MCF-7	breast:
14	chr8:111662012..111664592-chr8:111665712..111669617,3	MCF-7	breast:
15	chr8:111669709..111671243-chr8:111673107..111675313,2	MCF-7	breast:
16	chr8:111426432..111429583-chr8:111430116..111432569,3	MCF-7	breast:
17	chr8:111564585..111566803-chr8:111570856..111572872,2	K562	blood:
18	chr15:38663825..38666657-chr8:111561522..111564455,2	MCF-7	breast:
19	chr7:153439451..153439951-chr8:111669137..111669684,2	MCF-7	breast:
20	chr20:47537126..47538714-chr8:111554238..111556097,2	MCF-7	breast:
21	chr8:111100909..111103732-chr8:111408499..111410564,2	K562	blood:
22	chr8:111669709..111671243-chr8:111673107..111675313,2	MCF-7	breast:
23	chr8:111575672..111578651-chr8:111595648..111598231,2	MCF-7	breast:
24	chr22:21987659..21988468-chr8:111631630..111632515,2	MCF-7	breast:
25	chr8:37622904..37623517-chr8:111713671..111714213,2	MCF-7	breast:
26	chr8:111632530..111634212-chr8:111646106..111648334,2	MCF-7	breast:
27	chr7:156803278..156804875-chr8:111542688..111545615,2	MCF-7	breast:
28	chr8:111681810..111684012-chr8:111686136..111688041,2	K562	blood:
29	chr8:111681810..111684012-chr8:111686136..111688041,2	K562	blood:
30	chr8:111444766..111447245-chr8:111451075..111453827,2	K562	blood:
31	chr8:111564585..111566803-chr8:111570856..111572872,2	K562	blood:
32	chr8:111554765..111555294-chr8:111669236..111669854,2	MCF-7	breast:
33	chr8:111662012..111664592-chr8:111665712..111669617,3	MCF-7	breast:
34	chr8:111365308..111365953-chr8:111842805..111843518,2	MCF-7	breast:
35	chr8:111705966..111708208-chr8:111719733..111721854,2	MCF-7	breast:
36	chr8:111714002..111715922-chr8:111718938..111720595,2	K562	blood:
37	chr8:111426582..111428380-chr8:111435676..111438119,2	K562	blood:
38	chr8:111597648..111599475-chr8:111601535..111603940,2	MCF-7	breast:
39	chr8:111705966..111708208-chr8:111719733..111721854,2	MCF-7	breast:
40	chr8:111365378..111366118-chr8:111834050..111834594,2	MCF-7	breast:
41	chr8:111327977..111330779-chr8:111340224..111342460,2	MCF-7	breast:
42	chr8:111667414..111669906-chr8:111688361..111690572,2	MCF-7	breast:
43	chr8:111338897..111341781-chr8:111343648..111346155,2	MCF-7	breast:
44	chr8:111629561..111631393-chr8:111634350..111636471,2	MCF-7	breast:
45	chr8:111665338..111666843-chr8:111677219..111678888,2	K562	blood:
46	chr8:111606860..111609172-chr8:111612437..111615361,2	K562	blood:
47	chr8:111365043..111367620-chr8:111553595..111556957,3	MCF-7	breast:
48	chr8:111426582..111428380-chr8:111435676..111438119,2	K562	blood:
49	chr8:111426432..111429583-chr8:111430116..111432569,3	MCF-7	breast:
50	chr8:111554765..111555294-chr8:111669236..111669854,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KCNV1-1	chr8:111361774-111361836	ENSG00000253956
2	lnc-KCNV1-1	chr8:111356682-111356824	ENSG00000253956
3	lnc-KCNV1-1	chr8:111346972-111347538	ENSG00000253956
4	lnc-RP11-422N16.3.1-5	chr8:111567637-111568747	NONHSAT128309

No data

Variant related genes	Relation type
ENSG00000253956	TF binding region
ENSG00000253107	TF binding region
ENSG00000253122	TF binding region
ENSG00000253956	CpG island
ENSG00000253107	CpG island
ENSG00000253122	CpG island
ENSG00000253122	chromatin interactions
ENSG00000198087	chromatin interactions
ENSG00000077514	chromatin interactions
ENSG00000124198	chromatin interactions
ENSG00000243479	chromatin interactions
ENSG00000130675	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000270761	chromatin interactions

Extended variants
information (count: 5746 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:5746 , 50 per page) page: 1 2 3 4 5 6 7 ... 115

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7832047	chr8:111342240-111342241	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs569798699	chr8:111342243-111342244	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs566112980	chr8:111342244-111342245	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs144120305	chr8:111342259-111342260	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs145999777	chr8:111342289-111342290	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs527671745	chr8:111342291-111342292	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs376808608	chr8:111342302-111342303	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs538164645	chr8:111342330-111342331	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs555109703	chr8:111342345-111342346	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs373380493	chr8:111342355-111342356	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs577427498	chr8:111342374-111342375	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs370698155	chr8:111342377-111342378	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs139881746	chr8:111342400-111342401	Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs538763554	chr8:111342402-111342403	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs542622248	chr8:111342449-111342450	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs577302170	chr8:111342462-111342463	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs540285729	chr8:111342467-111342468	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs546268171	chr8:111342484-111342485	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs560262334	chr8:111342487-111342488	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs562876061	chr8:111342528-111342529	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs561456946	chr8:111342532-111342533	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs77790906	chr8:111342547-111342548	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs530795520	chr8:111342551-111342552	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs550618908	chr8:111342579-111342580	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs561111363	chr8:111342599-111342600	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs558484533	chr8:111342618-111342619	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs189756572	chr8:111342627-111342628	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs151148511	chr8:111342635-111342636	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs566276141	chr8:111342682-111342683	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs538348965	chr8:111342720-111342721	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs144245226	chr8:111342756-111342757	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs551713077	chr8:111342787-111342788	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs367614900	chr8:111342805-111342806	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs538502461	chr8:111342819-111342820	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs80106034	chr8:111342840-111342841	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs370313140	chr8:111342860-111342861	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs180691792	chr8:111342901-111342902	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs140043595	chr8:111342902-111342903	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs185076136	chr8:111342913-111342914	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs190254363	chr8:111342922-111342923	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs534909845	chr8:111342931-111342932	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs183193648	chr8:111342952-111342953	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs562839682	chr8:111342994-111342995	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs573961545	chr8:111343032-111343033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs7836358	chr8:111343056-111343057	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs375962170	chr8:111343059-111343060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs561066572	chr8:111343063-111343064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs188481570	chr8:111343096-111343097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs529893669	chr8:111343108-111343109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs546341040	chr8:111343131-111343132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

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
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	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
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21611746	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
Chronic myeloid leukemia	21384125	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Breast cancer	21364760	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:111340800-111342600	Enhancers	Pancreatic Islets	Pancreatic Islet
2	chr8:111340800-111342600	Enhancers	Fetal Lung	lung
3	chr8:111341000-111342400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr8:111341000-111342400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr8:111341200-111342400	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr8:111341400-111342400	Weak transcription	Rectal Mucosa Donor 31	rectum
7	chr8:111341600-111342400	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
8	chr8:111341600-111342600	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr8:111341800-111342400	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr8:111341800-111343000	Enhancers	HepG2	liver
11	chr8:111342200-111342400	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr8:111342200-111342400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr8:111342200-111342800	Enhancers	Liver	Liver
14	chr8:111342400-111342600	Enhancers	Rectal Mucosa Donor 31	rectum
15	chr8:111342400-111342800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr8:111342400-111342800	Active TSS	Rectal Mucosa Donor 29	rectum
17	chr8:111342800-111345400	Weak transcription	NHEK	skin
18	chr8:111345000-111346000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr8:111345000-111347600	Enhancers	HMEC	breast
20	chr8:111345200-111347600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr8:111345200-111347600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr8:111345400-111346000	Enhancers	NHEK	skin
23	chr8:111345600-111347400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr8:111346000-111346400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr8:111346000-111346400	Weak transcription	NHEK	skin
26	chr8:111346400-111347400	Enhancers	NHEK	skin
27	chr8:111346400-111347600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr8:111346600-111347000	Enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr8:111346600-111347400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr8:111347600-111350600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr8:111347600-111354200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr8:111350600-111350800	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr8:111354200-111354800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr8:111354800-111380600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr8:111359000-111359800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr8:111380600-111380800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr8:111413400-111413800	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr8:111413600-111414000	Enhancers	Fetal Intestine Small	intestine
39	chr8:111459800-111460000	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr8:111460600-111460800	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr8:111464200-111464600	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr8:111464200-111464800	Enhancers	H1 Cell Line	embryonic stem cell
43	chr8:111464200-111464800	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr8:111464200-111464800	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr8:111464600-111465400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr8:111465400-111466600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr8:111466600-111467200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr8:111466800-111467200	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
49	chr8:111469200-111469400	Enhancers	Placenta Amnion	Placenta Amnion
50	chr8:111469600-111470600	Weak transcription	Placenta Amnion	Placenta Amnion

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