Variant report

Variant	nsv891295
Chromosome Location	chr8:111852200-112163801
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1365)
CpG islands
(count:305)
Chromatin interactive
region (count:114)
LncRNA
region (count:36)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1365 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:111930749-111931038	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:111861128-111861289	K562	blood:	n/a	n/a
3	ARID3A	chr8:112055951-112056163	K562	blood:	n/a	n/a
4	ARID3A	chr8:111860272-111860903	HepG2	liver:	n/a	chr8:111860332-111860348
5	ARID3A	chr8:112005161-112005584	HepG2	liver:	n/a	n/a
6	ARID3A	chr8:111927195-111927263	K562	blood:	n/a	n/a
7	ARID3A	chr8:111860419-111860636	K562	blood:	n/a	n/a
8	ATF1	chr8:111906691-111907234	K562	blood:	n/a	n/a
9	ATF1	chr8:112055891-112056208	K562	blood:	n/a	n/a
10	ATF1	chr8:111875900-111876067	K562	blood:	n/a	n/a
11	ATF1	chr8:112132480-112132510	K562	blood:	n/a	n/a
12	ATF1	chr8:112052514-112052777	K562	blood:	n/a	n/a
13	ATF2	chr8:112162891-112163440	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr8:112162917-112163564	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF3	chr8:111860291-111860669	K562	blood:	n/a	n/a
16	BACH1	chr8:111914552-111914921	K562	blood:	n/a	chr8:111914731-111914745
17	BACH1	chr8:112001168-112001459	K562	blood:	n/a	n/a
18	BACH1	chr8:112001137-112001412	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr8:111907020-111907275	K562	blood:	n/a	n/a
20	BACH1	chr8:111914556-111914922	H1-hESC	embryonic stem cell:	n/a	chr8:111914731-111914745
21	BATF	chr8:111887230-111887546	GM12878	blood:	n/a	chr8:111887372-111887383 chr8:111887369-111887379 chr8:111887386-111887397
22	BATF	chr8:112113181-112113447	GM12878	blood:	n/a	n/a
23	BATF	chr8:111887241-111887473	GM12878	blood:	n/a	chr8:111887372-111887383 chr8:111887369-111887379 chr8:111887386-111887397
24	BATF	chr8:111860419-111860570	GM12878	blood:	n/a	chr8:111860544-111860554
25	BCL11A	chr8:112162971-112163355	H1-hESC	embryonic stem cell:	n/a	n/a
26	BCL11A	chr8:112162999-112163239	H1-hESC	embryonic stem cell:	n/a	n/a
27	BCL3	chr8:112032257-112032818	K562	blood:	n/a	n/a
28	BCLAF1	chr8:112045287-112045677	K562	blood:	n/a	n/a
29	BCLAF1	chr8:112049253-112049676	K562	blood:	n/a	n/a
30	BCLAF1	chr8:112047895-112049222	K562	blood:	n/a	n/a
31	BCLAF1	chr8:112051891-112052761	K562	blood:	n/a	n/a
32	BCLAF1	chr8:112050664-112051080	K562	blood:	n/a	n/a
33	BCLAF1	chr8:112051085-112051725	K562	blood:	n/a	n/a
34	BHLHE40	chr8:112113324-112113447	K562	blood:	n/a	n/a
35	BHLHE40	chr8:111927453-111927498	GM12878	blood:	n/a	n/a
36	BHLHE40	chr8:111906788-111907219	K562	blood:	n/a	n/a
37	BRCA1	chr8:111906219-111906223	HepG2	liver:	n/a	n/a
38	BRCA1	chr8:112152605-112152831	H1-hESC	embryonic stem cell:	n/a	n/a
39	BRCA1	chr8:111880545-111880672	Hela-S3	cervix:	n/a	n/a
40	CBX3	chr8:112052302-112052706	K562	blood:	n/a	n/a
41	CBX3	chr8:112112808-112113129	K562	blood:	n/a	n/a
42	CBX3	chr8:111906683-111907203	K562	blood:	n/a	n/a
43	CCNT2	chr8:112098454-112098654	K562	blood:	n/a	n/a
44	CCNT2	chr8:112053174-112053372	K562	blood:	n/a	n/a
45	CCNT2	chr8:111906640-111907232	K562	blood:	n/a	n/a
46	CCNT2	chr8:112035228-112035538	K562	blood:	n/a	n/a
47	CEBPB	chr8:112058029-112058214	K562	blood:	n/a	n/a
48	CEBPB	chr8:111928051-111928091	K562	blood:	n/a	n/a
49	CEBPB	chr8:112003382-112003710	HepG2	liver:	n/a	chr8:112003559-112003570 chr8:112003465-112003477
50	CEBPB	chr8:112003416-112003715	K562	blood:	n/a	chr8:112003559-112003570 chr8:112003465-112003477

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:112163550-112163600	GM12891	blood:	n/a
2	chr8:111906503-111906553	RPTEC	kidney:	n/a
3	chr8:112052376-112052426	PrEC	prostate:	n/a
4	chr8:112052376-112052426	HCM	heart:	n/a
5	chr8:112052376-112052426	HIPEpiC	eye:	n/a
6	chr8:112163550-112163600	AG04450	lung:	fetal
7	chr8:112163550-112163600	HMEC	breast:	n/a
8	chr8:112053139-112053189	HMEC	breast:	n/a
9	chr8:112053139-112053189	RPTEC	kidney:	n/a
10	chr8:112053356-112053406	BJ	skin:	n/a
11	chr8:111906503-111906553	SK-N-MC	brain:	n/a
12	chr8:112163550-112163600	HCT-116	colon:	n/a
13	chr8:111906503-111906553	AG04450	lung:	fetal
14	chr8:112052376-112052426	GM12892	blood:	n/a
15	chr8:112052376-112052426	MCF-7	breast:	n/a
16	chr8:112052376-112052426	U87	brain:	n/a
17	chr8:112053139-112053189	HepG2	liver:	n/a
18	chr8:112052376-112052426	HMEC	breast:	n/a
19	chr8:112052376-112052426	HRCEpiC	kidney:	n/a
20	chr8:112053139-112053189	PANC-1	pancreas:	n/a
21	chr8:112052376-112052426	Hela-S3	cervix:	n/a
22	chr8:111906503-111906553	MCF10A-Er-Src	breast:	n/a
23	chr8:112052376-112052426	Hepatocyte	liver:	n/a
24	chr8:111906503-111906553	NHDF-neo	bronchial:	n/a
25	chr8:112053139-112053189	AG09309	skin:	n/a
26	chr8:112053356-112053406	GM12892	blood:	n/a
27	chr8:112053356-112053406	SK-N-SH_RA	brain:	n/a
28	chr8:112052376-112052426	RPTEC	kidney:	n/a
29	chr8:112053139-112053189	H1-hESC	embryonic stem cell:	embryo
30	chr8:111906503-111906553	AG10803	skin:	n/a
31	chr8:112052376-112052426	AG09309	skin:	n/a
32	chr8:112163550-112163600	NHBE	bronchial:	n/a
33	chr8:111906503-111906553	AoSMC	blood vessel:	n/a
34	chr8:112053356-112053406	A549	lung:	n/a
35	chr8:112053139-112053189	HL-60	blood:	n/a
36	chr8:112053356-112053406	LNCaP	prostate:	n/a
37	chr8:112053356-112053406	NH-A	brain:	n/a
38	chr8:112053139-112053189	HNPCEpiC	eye:	n/a
39	chr8:112163550-112163600	CMK	blood:	n/a
40	chr8:111906503-111906553	GM12878	blood:	n/a
41	chr8:112053139-112053189	SKMC	muscle:	n/a
42	chr8:111906503-111906553	AG09309	skin:	n/a
43	chr8:112053139-112053189	ovcar-3	ovarian:	n/a
44	chr8:112163550-112163600	NHDF-neo	bronchial:	n/a
45	chr8:112163550-112163600	BE2_C	brain:	n/a
46	chr8:112163550-112163600	SK-N-MC	brain:	n/a
47	chr8:112053356-112053406	HRE	kidney:	n/a
48	chr8:112163550-112163600	MCF10A-Er-Src	breast:	n/a
49	chr8:112163550-112163600	ECC-1	luminal epithelium:	n/a
50	chr8:112163550-112163600	A549	lung:	n/a

(count:114 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr8:112048936..112050603-chr8:112056318..112058671,2	K562	blood:
2	chr8:112037306..112039469-chr8:112041170..112043078,2	K562	blood:
3	chr8:111855787..111857322-chr8:111859376..111860898,2	MCF-7	breast:
4	chr8:112037306..112039469-chr8:112041170..112043078,2	K562	blood:
5	chr8:112152279..112153092-chr8:121617588..121618297,2	MCF-7	breast:
6	chr8:112127583..112130124-chr8:112133579..112135146,2	MCF-7	breast:
7	chr8:112024408..112026830-chr8:112028447..112030493,2	K562	blood:
8	chr8:111977359..111979519-chr8:111986099..111987901,2	K562	blood:
9	chr8:111952441..111954881-chr8:111958633..111961171,2	K562	blood:
10	chr8:111918636..111921932-chr8:111925930..111928582,3	K562	blood:
11	chr8:112152245..112153161-chr8:112248220..112248923,2	MCF-7	breast:
12	chr8:112073611..112075207-chr8:112079150..112081817,2	MCF-7	breast:
13	chr8:111986722..111988349-chr8:112001568..112003641,2	K562	blood:
14	chr8:112054463..112057447-chr8:112061238..112063289,2	K562	blood:
15	chr8:111877803..111878653-chr8:112126153..112126716,2	MCF-7	breast:
16	chr8:112048936..112050603-chr8:112056318..112058671,2	K562	blood:
17	chr8:112154689..112157253-chr8:112157958..112160941,2	MCF-7	breast:
18	chr8:111905656..111907856-chr8:111909688..111913737,4	K562	blood:
19	chr8:111842914..111844843-chr8:111916183..111918986,2	MCF-7	breast:
20	chr8:112112298..112113981-chr8:112264995..112266040,10	MCF-7	breast:
21	chr8:111913749..111916185-chr8:111918003..111920287,2	MCF-7	breast:
22	chr1:120421655..120422591-chr8:112129482..112130279,2	MCF-7	breast:
23	chr8:112121761..112124184-chr8:112126207..112129085,2	K562	blood:
24	chr8:112024408..112026830-chr8:112028447..112030493,2	K562	blood:
25	chr8:111913749..111916185-chr8:111918003..111920287,2	MCF-7	breast:
26	chr8:112054463..112057447-chr8:112061238..112063289,2	K562	blood:
27	chr8:112092554..112095223-chr8:112096856..112098486,2	MCF-7	breast:
28	chr8:111877803..111878676-chr8:112126153..112126932,3	MCF-7	breast:
29	chr8:111906809..111908563-chr8:111915252..111917279,2	K562	blood:
30	chr8:111668947..111669607-chr8:111877933..111878646,3	MCF-7	breast:
31	chr8:111907063..111908580-chr8:111914627..111917279,2	K562	blood:
32	chr8:112121761..112124184-chr8:112126207..112129085,2	K562	blood:
33	chr8:111923379..111925877-chr8:111931950..111934366,2	MCF-7	breast:
34	chr8:111929502..111932269-chr8:111933954..111936192,2	MCF-7	breast:
35	chr8:111948692..111950464-chr8:111998456..112000368,2	MCF-7	breast:
36	chr8:112040792..112044019-chr8:112049363..112052232,3	K562	blood:
37	chr8:112092554..112095223-chr8:112096856..112098486,2	MCF-7	breast:
38	chr8:111853597..111856569-chr8:111856769..111860452,3	MCF-7	breast:
39	chr8:111877768..111878423-chr8:111945734..111946406,2	MCF-7	breast:
40	chr8:111907063..111908580-chr8:111914627..111917279,2	K562	blood:
41	chr8:111929502..111932269-chr8:111933954..111936192,2	MCF-7	breast:
42	chr8:111870941..111873511-chr8:111873961..111876570,2	K562	blood:
43	chr8:112046473..112049277-chr8:112050883..112054393,4	K562	blood:
44	chr8:112049920..112051426-chr8:112052995..112055202,2	K562	blood:
45	chr8:111986722..111988349-chr8:112001568..112003641,2	K562	blood:
46	chr8:111952441..111954881-chr8:111958633..111961171,2	K562	blood:
47	chr8:112126432..112126980-chr8:112164515..112165028,2	MCF-7	breast:
48	chr8:112073611..112075207-chr8:112079150..112081817,2	MCF-7	breast:
49	chr8:112115345..112116966-chr8:112124670..112126786,2	MCF-7	breast:
50	chr8:112040792..112044019-chr8:112049363..112052232,3	K562	blood:

(count:36 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KCNV1-7	chr8:112086066-112086174	l_3667_chr8:112084787-112108928_brain
2	lnc-KCNV1-7	chr8:112096343-112096437	l_3667_chr8:112084787-112108928_brain
3	lnc-RP11-422N16.3.1-6	chr8:112000263-112000924	NONHSAT128319
4	lnc-KCNV1-2	chr8:111995179-111995369	ENSG00000253877
5	lnc-CSMD3-3	chr8:112111190-112111368	ENSG00000253103
6	lnc-RP11-422N16.3.1-6	chr8:112002113-112002710	NONHSAT128319
7	lnc-KCNV1-2	chr8:112039535-112039662	ENSG00000253877
8	lnc-KCNV1-2	chr8:112027133-112027261	ENSG00000253877
9	lnc-KCNV1-2	chr8:112015643-112015679	XLOC_007182
10	lnc-KCNV1-2	chr8:111993626-111995369	XLOC_007182
11	lnc-KCNV1-2	chr8:112015643-112015679	XLOC_007182
12	lnc-KCNV1-2	chr8:112015643-112015679	ENSG00000253877
13	lnc-KCNV1-2	chr8:112015643-112015679	XLOC_007182
14	lnc-KCNV1-2	chr8:112015643-112015679	ENSG00000253877
15	lnc-KCNV1-2	chr8:112017759-112017878	ENSG00000253877
16	lnc-KCNV1-7	chr8:112108711-112108928	l_3667_chr8:112084787-112108928_brain
17	lnc-KCNV1-2	chr8:111949919-111949956	ENSG00000253877
18	lnc-KCNV1-7	chr8:112084788-112084855	l_3667_chr8:112084787-112108928_brain
19	lnc-RP11-422N16.3.1-6	chr8:112000263-112000924	FPKM1_group_31989_transcript_3
20	lnc-CSMD3-3	chr8:112125661-112125749	ENSG00000253103
21	lnc-KCNV1-2	chr8:111991098-111995369	XLOC_007182
22	lnc-KCNV1-2	chr8:112016890-112016998	XLOC_007182
23	lnc-KCNV1-2	chr8:112039535-112039752	XLOC_007182
24	lnc-KCNV1-2	chr8:112016890-112016998	ENSG00000253877
25	lnc-CSMD3-3	chr8:112128764-112128829	ENSG00000253103
26	lnc-RP11-422N16.3.1-6	chr8:112000448-112001045	FPKM1_group_31989_transcript_3
27	lnc-KCNV1-7	chr8:112086929-112087054	l_3667_chr8:112084787-112108928_brain
28	lnc-KCNV1-2	chr8:112039535-112039752	XLOC_007182
29	lnc-KCNV1-2	chr8:112017759-112017878	XLOC_007182
30	lnc-KCNV1-2	chr8:112017759-112017878	XLOC_007182
31	lnc-KCNV1-2	chr8:111994744-111995369	XLOC_007182
32	lnc-KCNV1-2	chr8:112017759-112017878	ENSG00000253877
33	lnc-KCNV1-2	chr8:112016890-112016917	XLOC_007182
34	lnc-KCNV1-2	chr8:112016890-112016998	ENSG00000253877
35	lnc-KCNV1-2	chr8:112039535-112039621	ENSG00000253877
36	lnc-KCNV1-2	chr8:112039535-112039641	XLOC_007182

No data

Variant related genes	Relation type
ENSG00000254241	TF binding region
ENSG00000253877	TF binding region
ENSG00000254241	CpG island
ENSG00000253877	CpG island
ENSG00000253877	chromatin interactions
ENSG00000253103	chromatin interactions
CDC42	miRNA target sites
ZFPM2	miRNA target sites
AADACL3	miRNA target sites
DNMT1	miRNA target sites
TFRC	miRNA target sites
ZEB2	miRNA target sites

Extended variants
information (count: 6322 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:6322 , 50 per page) page: 1 2 3 4 5 6 7 ... 127

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs191330526	chr8:111860068-111860069	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs552613339	chr8:111860119-111860120	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs540284740	chr8:111860168-111860169	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs569315173	chr8:111860178-111860179	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs183625372	chr8:111860179-111860180	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs4607577	chr8:111860191-111860192	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs113887151	chr8:111860238-111860239	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs142864888	chr8:111860245-111860246	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs534146807	chr8:111860248-111860249	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs151048169	chr8:111860259-111860260	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs188620973	chr8:111860323-111860324	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs539781085	chr8:111860338-111860339	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs549039599	chr8:111860339-111860340	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs192535491	chr8:111860350-111860351	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs7004627	chr8:111860361-111860362	Enhancers Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs371477272	chr8:111860381-111860382	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs541892656	chr8:111860460-111860461	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs561643148	chr8:111860580-111860581	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs572176471	chr8:111860594-111860595	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs77171107	chr8:111860600-111860601	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs542671834	chr8:111860658-111860659	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs78030650	chr8:111860707-111860708	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs11774323	chr8:111860724-111860725	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs543787261	chr8:111860787-111860788	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs7816438	chr8:111860818-111860819	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs531646386	chr8:111860889-111860890	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs551282015	chr8:111860894-111860895	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs548631481	chr8:111860956-111860957	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs568485868	chr8:111860966-111860967	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs527844000	chr8:111860968-111860969	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs571402811	chr8:111861001-111861002	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs184516234	chr8:111861002-111861003	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs7009284	chr8:111861006-111861007	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs539722169	chr8:111861011-111861012	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs377642656	chr8:111861018-111861019	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs186720768	chr8:111861062-111861063	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs115277482	chr8:111861072-111861073	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs191139474	chr8:111861117-111861118	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs527501996	chr8:111861192-111861193	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs572056608	chr8:111861238-111861239	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs60402522	chr8:111861249-111861250	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs557981839	chr8:111861338-111861339	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs372158805	chr8:111861388-111861389	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs116874399	chr8:111861389-111861390	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs540781953	chr8:111861442-111861443	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs373510058	chr8:111861443-111861444	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs184399657	chr8:111861448-111861449	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs145301771	chr8:111861453-111861454	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs531705589	chr8:111861465-111861466	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs541864956	chr8:111861483-111861484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

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
Breast cancer	22522925	CNVD
Neuroticism	17667963	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	21163964	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:398 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:111860000-111860200	Enhancers	Fetal Intestine Large	intestine
2	chr8:111860000-111860600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr8:111860000-111860600	Enhancers	Muscle Satellite Cultured Cells	--
4	chr8:111860000-111861400	Enhancers	HUVEC	blood vessel
5	chr8:111860200-111860600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr8:111860200-111860800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr8:111860200-111860800	Active TSS	A549	lung
8	chr8:111860200-111861200	Weak transcription	Fetal Intestine Large	intestine
9	chr8:111860200-111862800	Enhancers	Fetal Intestine Small	intestine
10	chr8:111860400-111860600	Enhancers	HSMM	muscle
11	chr8:111860400-111861000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr8:111860600-111860800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr8:111860600-111861000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr8:111860600-111861000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
15	chr8:111860600-111861000	Flanking Active TSS	HSMM	muscle
16	chr8:111860600-111861200	Enhancers	Hela-S3	cervix
17	chr8:111860600-111861200	Enhancers	HSMMtube	muscle
18	chr8:111860600-111861400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr8:111860600-111861400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
20	chr8:111860600-111861400	Enhancers	HepG2	liver
21	chr8:111860600-111861400	Enhancers	NH-A	brain
22	chr8:111860600-111861400	Enhancers	NHDF-Ad	bronchial
23	chr8:111860800-111861000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr8:111860800-111861400	Flanking Active TSS	A549	lung
25	chr8:111861000-111861200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr8:111861000-111861400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr8:111861000-111861400	Enhancers	Muscle Satellite Cultured Cells	--
28	chr8:111861000-111861400	Enhancers	HSMM	muscle
29	chr8:111861200-111861400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr8:111861200-111861400	Enhancers	Fetal Intestine Large	intestine
31	chr8:111861400-111861800	Weak transcription	Fetal Intestine Large	intestine
32	chr8:111861400-111862400	Enhancers	A549	lung
33	chr8:111861800-111862200	Enhancers	Fetal Intestine Large	intestine
34	chr8:111862000-111862800	Enhancers	Brain Germinal Matrix	brain
35	chr8:111862200-111862800	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr8:111862400-111864600	Weak transcription	A549	lung
37	chr8:111862600-111863000	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr8:111864600-111865800	Enhancers	A549	lung
39	chr8:111865600-111865800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr8:111865800-111872200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr8:111871400-111872600	Enhancers	Fetal Intestine Large	intestine
42	chr8:111871800-111872600	Enhancers	Fetal Intestine Small	intestine
43	chr8:111872200-111872600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr8:111872200-111873800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
45	chr8:111872600-111875200	Weak transcription	Fetal Intestine Large	intestine
46	chr8:111875000-111877200	Enhancers	Fetal Intestine Small	intestine
47	chr8:111875200-111876000	Enhancers	Fetal Intestine Large	intestine
48	chr8:111875600-111876400	Enhancers	Brain Anterior Caudate	brain
49	chr8:111875600-111876600	Enhancers	Fetal Lung	lung
50	chr8:111875800-111876200	Enhancers	K562	blood

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