Variant report

Variant	nsv1059775
Chromosome Location	chr18:11892845-11911143
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:615)
CpG islands
(count:916)
Chromatin interactive
region (count:34)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:615 , 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	chr18:11908135-11908358	HepG2	liver:	n/a	n/a
2	ARID3A	chr18:11902099-11902147	K562	blood:	n/a	n/a
3	ARID3A	chr18:11907350-11907482	K562	blood:	n/a	n/a
4	ARID3A	chr18:11909461-11909993	HepG2	liver:	n/a	n/a
5	ARID3A	chr18:11907986-11908404	K562	blood:	n/a	n/a
6	ATF2	chr18:11908285-11908572	GM12878	blood:	n/a	n/a
7	ATF2	chr18:11908044-11908868	GM12878	blood:	n/a	n/a
8	BACH1	chr18:11905555-11905819	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr18:11908181-11908512	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr18:11908961-11909164	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr18:11907432-11907571	K562	blood:	n/a	n/a
12	BATF	chr18:11909467-11909856	GM12878	blood:	n/a	n/a
13	BATF	chr18:11909547-11909800	GM12878	blood:	n/a	n/a
14	BCLAF1	chr18:11908015-11908934	GM12878	blood:	n/a	chr18:11908598-11908611
15	BCLAF1	chr18:11908000-11909062	GM12878	blood:	n/a	chr18:11908598-11908611
16	BHLHE40	chr18:11908100-11908816	GM12878	blood:	n/a	chr18:11908550-11908566
17	BHLHE40	chr18:11901955-11902212	K562	blood:	n/a	n/a
18	BHLHE40	chr18:11908027-11909281	K562	blood:	n/a	chr18:11908550-11908566
19	BRCA1	chr18:11908243-11908347	HepG2	liver:	n/a	n/a
20	BRCA1	chr18:11907985-11908720	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr18:11909178-11909180	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr18:11908489-11908538	GM12878	blood:	n/a	n/a
23	CCNT2	chr18:11908140-11909117	K562	blood:	n/a	n/a
24	CCNT2	chr18:11901846-11902228	K562	blood:	n/a	n/a
25	CEBPB	chr18:11909709-11910038	HepG2	liver:	n/a	n/a
26	CEBPB	chr18:11908096-11908743	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr18:11909791-11909856	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr18:11900992-11901024	K562	blood:	n/a	n/a
29	CEBPD	chr18:11901876-11902177	K562	blood:	n/a	n/a
30	CEBPD	chr18:11908291-11908667	HepG2	liver:	n/a	n/a
31	CEBPD	chr18:11901868-11902237	K562	blood:	n/a	n/a
32	CHD1	chr18:11907360-11908142	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD1	chr18:11908052-11909421	GM12878	blood:	n/a	chr18:11909115-11909125 chr18:11908760-11908770
34	CHD1	chr18:11908460-11908668	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr18:11908280-11908784	HepG2	liver:	n/a	chr18:11908760-11908770
36	CHD2	chr18:11908686-11908750	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD2	chr18:11908140-11908757	K562	blood:	n/a	n/a
38	CHD2	chr18:11908142-11908874	Hela-S3	cervix:	n/a	chr18:11908760-11908770
39	CHD2	chr18:11908144-11909245	GM12878	blood:	n/a	chr18:11909115-11909125 chr18:11908760-11908770
40	CREB1	chr18:11908136-11908583	A549	lung:	n/a	n/a
41	CREB1	chr18:11908095-11909057	GM12878	blood:	n/a	n/a
42	CTBP2	chr18:11908185-11908778	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr18:11908727-11908736	MCF-7	breast:	n/a	n/a
44	CTCF	chr18:11908620-11908770	AG04449	skin:	n/a	n/a
45	CTCF	chr18:11908280-11908430	HRE	kidney:	n/a	n/a
46	CTCF	chr18:11908640-11908790	HMEC	breast:	n/a	n/a
47	CTCF	chr18:11908600-11908750	GM12870	blood:	n/a	n/a
48	CTCF	chr18:11908540-11908690	HCM	heart:	n/a	n/a
49	CTCF	chr18:11908260-11908410	SAEC	small airway:	n/a	n/a
50	CTCF	chr18:11908680-11908830	GM12871	blood:	n/a	n/a

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:11908803-11908853	HepG2	liver:	n/a
2	chr18:11908803-11908853	HepG2	liver:	n/a
3	chr18:11908772-11908822	NH-A	brain:	n/a
4	chr18:11908811-11908861	SKMC	muscle:	n/a
5	chr18:11908331-11908381	HMEC	breast:	n/a
6	chr18:11908695-11908745	HAEpiC	amniotic membrane:	n/a
7	chr18:11908251-11908301	HNPCEpiC	eye:	n/a
8	chr18:11908320-11908370	SK-N-MC	brain:	n/a
9	chr18:11908900-11908950	Hela-S3	cervix:	n/a
10	chr18:11908251-11908301	AG04449	skin:	fetal
11	chr18:11908900-11908950	AG10803	skin:	n/a
12	chr18:11908827-11908877	ECC-1	luminal epithelium:	n/a
13	chr18:11908331-11908381	HNPCEpiC	eye:	n/a
14	chr18:11908320-11908370	AG04450	lung:	fetal
15	chr18:11908320-11908370	BE2_C	brain:	n/a
16	chr18:11908320-11908370	K562	blood:	n/a
17	chr18:11908772-11908822	HUVEC	blood vessel:	n/a
18	chr18:11909052-11909102	AG04449	skin:	fetal
19	chr18:11909052-11909102	BE2_C	brain:	n/a
20	chr18:11908900-11908950	NB4	blood:	n/a
21	chr18:11908320-11908370	HCF	heart:	n/a
22	chr18:11908900-11908950	BE2_C	brain:	n/a
23	chr18:11909052-11909102	NT2-D1	testis:	n/a
24	chr18:11908827-11908877	HAEpiC	amniotic membrane:	n/a
25	chr18:11909008-11909058	SAEC	small airway:	n/a
26	chr18:11908320-11908370	Hepatocyte	liver:	n/a
27	chr18:11908652-11908702	HepG2	liver:	n/a
28	chr18:11908772-11908822	HAEpiC	amniotic membrane:	n/a
29	chr18:11908900-11908950	PANC-1	pancreas:	n/a
30	chr18:11908695-11908745	HEK293	kidney:	embryo
31	chr18:11908811-11908861	HCPEpiC	choroid plexus:	n/a
32	chr18:11908772-11908822	BE2_C	brain:	n/a
33	chr18:11909052-11909102	GM12878	blood:	n/a
34	chr18:11908320-11908370	HEEpiC	esophagus:	n/a
35	chr18:11908652-11908702	ProgFib	skin:	n/a
36	chr18:11908181-11908231	AG10803	skin:	n/a
37	chr18:11908251-11908301	PrEC	prostate:	n/a
38	chr18:11908811-11908861	GM12891	blood:	n/a
39	chr18:11909052-11909102	SK-N-SH_RA	brain:	n/a
40	chr18:11908803-11908853	HL-60	blood:	n/a
41	chr18:11909634-11909684	HIPEpiC	eye:	n/a
42	chr18:11909052-11909102	AG10803	skin:	n/a
43	chr18:11909634-11909684	MCF10A-Er-Src	breast:	n/a
44	chr18:11908695-11908745	HPAEpiC	pulmonary alveolar:	n/a
45	chr18:11908251-11908301	SK-N-SH	brain:	n/a
46	chr18:11908827-11908877	AG09319	gingival:	n/a
47	chr18:11908900-11908950	IMR90	lung:	fetal
48	chr18:11908331-11908381	ProgFib	skin:	n/a
49	chr18:11908695-11908745	GM19239	blood:	n/a
50	chr18:11908320-11908370	Jurkat	blood:	n/a

(count:34 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:11908077..11908808-chr3:73160102..73160621,2	Hela-S3	cervix:
2	chr18:11899516..11901029-chr18:11908171..11909985,2	MCF-7	breast:
3	chr18:11898547..11901109-chr18:11904202..11906126,2	K562	blood:
4	chr18:11902690..11905411-chr18:11905422..11908532,4	K562	blood:
5	chr18:11892388..11894879-chr18:11897284..11900106,3	K562	blood:
6	chr18:11899621..11904572-chr18:11905422..11909871,7	K562	blood:
7	chr18:11848894..11852838-chr18:11907232..11909901,3	MCF-7	breast:
8	chr18:11906869..11908788-chr18:11979428..11982249,2	K562	blood:
9	chr18:11902690..11905411-chr18:11905422..11908532,4	K562	blood:
10	chr18:11899621..11904572-chr18:11905422..11909871,7	K562	blood:
11	chr18:11893379..11895181-chr18:11897830..11899387,2	K562	blood:
12	chr18:11908518..11911302-chr18:12009524..12011140,2	MCF-7	breast:
13	chr18:11905031..11907114-chr18:12010048..12012085,2	K562	blood:
14	chr18:11853727..11856399-chr18:11905762..11908760,2	K562	blood:
15	chr18:11899627..11904640-chr18:11906955..11910092,5	MCF-7	breast:
16	chr14:100842502..100843242-chr18:11908364..11908922,2	Hela-S3	cervix:
17	chr17:8076437..8076995-chr18:11908144..11908909,2	Hela-S3	cervix:
18	chr18:11905898..11908508-chr18:11980358..11982828,3	K562	blood:
19	chr18:11890272..11892139-chr18:11894063..11896941,2	MCF-7	breast:
20	chr18:11851217..11853122-chr18:11907362..11910210,4	MCF-7	breast:
21	chr10:75543773..75546549-chr18:11908703..11911397,2	MCF-7	breast:
22	chr18:11848334..11851734-chr18:11906595..11909240,3	K562	blood:
23	chr18:11906925..11910950-chr18:11978930..11983753,7	MCF-7	breast:
24	chr18:11898547..11901109-chr18:11904202..11906126,2	K562	blood:
25	chr18:11907153..11910661-chr18:11980045..11982514,4	MCF-7	breast:
26	chr18:11899627..11904640-chr18:11906955..11910092,5	MCF-7	breast:
27	chr12:56550673..56553390-chr18:11908435..11911361,2	MCF-7	breast:
28	chr18:11892388..11894879-chr18:11897284..11900106,3	K562	blood:
29	chr18:11849809..11852493-chr18:11906595..11908569,3	K562	blood:
30	chr18:11901497..11903544-chr18:11908058..11909728,2	MCF-7	breast:
31	chr18:11893379..11895181-chr18:11897830..11899387,2	K562	blood:
32	chr18:11885563..11889310-chr18:11906331..11909961,4	MCF-7	breast:
33	chr18:11901497..11903544-chr18:11908058..11909728,2	MCF-7	breast:
34	chr18:11893913..11896539-chr18:11907157..11909387,3	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MPPE1-1	chr18:11910714-11910861	XLOC_012771
2	lnc-GNAL-1	chr18:11908711-11909222	ENSG00000273141.1
3	lnc-MPPE1-1	chr18:11910633-11910861	ENSG00000267079.1
4	lnc-AP002414.1.1-5	chr18:11902779-11902855	NONHSAT058329
5	lnc-AP002414.1.1-5	chr18:11908201-11908317	NONHSAT058325
6	lnc-AP002414.1.1-5	chr18:11906203-11906308	NONHSAT058325
7	lnc-AP002414.1.1-5	chr18:11907895-11908275	NONHSAT058329
8	lnc-AP002414.1.1-5	chr18:11897157-11897355	NONHSAT058325
9	lnc-AP002414.1.1-5	chr18:11906202-11906308	NONHSAT058329

No data

Variant related genes	Relation type
ENSG00000273141	TF binding region
MPPE1	TF binding region
ENSG00000273141	CpG island
MPPE1	CpG island
ENSG00000273141	chromatin interactions
ENSG00000092841	chromatin interactions
ENSG00000257809	chromatin interactions
ENSG00000154889	chromatin interactions
ENSG00000140105	chromatin interactions
ENSG00000141401	chromatin interactions
ENSG00000214655	chromatin interactions
ENSG00000255112	chromatin interactions
ENSG00000223247	chromatin interactions
ENSG00000196465	chromatin interactions
ENSG00000200463	chromatin interactions
ENSG00000176473	chromatin interactions
ENSG00000267165	chromatin interactions

Extended variants
information (count: 821 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:821 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3974590	chr18:11892845-11892846	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs12457818	chr18:11892860-11892861	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs12455436	chr18:11892913-11892914	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs549761247	chr18:11892948-11892949	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs569368305	chr18:11892962-11892963	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs539492353	chr18:11892990-11892991	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs557889884	chr18:11893053-11893054	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs541111667	chr18:11893060-11893061	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs568144363	chr18:11893118-11893119	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs184368656	chr18:11893125-11893126	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs12458375	chr18:11893142-11893143	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs555447472	chr18:11893219-11893220	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs573856509	chr18:11893221-11893222	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs12456011	chr18:11893227-11893228	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs6650615	chr18:11893317-11893318	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs139716216	chr18:11893321-11893322	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs536517928	chr18:11893333-11893334	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs111730016	chr18:11893342-11893343	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs673735	chr18:11893391-11893392	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs76849648	chr18:11893431-11893432	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs374809786	chr18:11893434-11893435	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs368133200	chr18:11893437-11893438	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs371941720	chr18:11893445-11893446	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs564233907	chr18:11893475-11893476	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs79229995	chr18:11893492-11893493	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs374298301	chr18:11893517-11893518	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs145728460	chr18:11893524-11893525	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs540212873	chr18:11893530-11893531	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs200895860	chr18:11893536-11893537	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs34932177	chr18:11893554-11893555	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs201095750	chr18:11893555-11893556	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs112600800	chr18:11893574-11893575	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs551014085	chr18:11893586-11893587	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs200623434	chr18:11893611-11893612	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs144361932	chr18:11893624-11893625	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs552043908	chr18:11893639-11893640	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs566568525	chr18:11893662-11893663	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs533901396	chr18:11893685-11893686	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs555384128	chr18:11893742-11893743	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs2277729	chr18:11893764-11893765	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs538113901	chr18:11893779-11893780	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs373417926	chr18:11893800-11893801	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs59240143	chr18:11893840-11893841	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs577911945	chr18:11893853-11893854	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs544802762	chr18:11893855-11893856	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs77920955	chr18:11893856-11893857	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs144499494	chr18:11893875-11893876	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs540346487	chr18:11893912-11893913	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs561720614	chr18:11893927-11893928	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs75880586	chr18:11893970-11893971	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Intellectual disability	22102821	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Acute myeloid leukemia	16864856	CNVD
Seminomas	18059402	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Kartagener syndrome	16639409	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Cancer	21183584	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Human rectal carcinomas	16397240	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16272173	CNVD
Colorectal cancer	19150955	CNVD
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
Autism	20808228	CNVD
lymphocytic leukemia	21291569	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	21922591	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	17377590	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Developmental delay	21147756	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16620391	CNVD
Myelofibrosis	22110671	CNVD
Retinoblastoma	21504564	CNVD
Glioma	17123091	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1149 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:11873200-11902000	Weak transcription	Fetal Heart	heart
2	chr18:11876800-11902600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr18:11877000-11902400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr18:11878200-11895000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
5	chr18:11878200-11902400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr18:11880000-11907600	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr18:11881600-11898400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
8	chr18:11881800-11906200	Strong transcription	Primary T helper cells fromperipheralblood	blood
9	chr18:11882400-11907000	Weak transcription	Small Intestine	intestine
10	chr18:11882800-11895600	Weak transcription	NHDF-Ad	bronchial
11	chr18:11883400-11897000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr18:11883600-11893600	Weak transcription	HUVEC	blood vessel
13	chr18:11883600-11896800	Strong transcription	Fetal Intestine Small	intestine
14	chr18:11883600-11907000	Weak transcription	NH-A	brain
15	chr18:11883800-11894200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
16	chr18:11883800-11898400	Strong transcription	Fetal Stomach	stomach
17	chr18:11884000-11893000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
18	chr18:11884000-11893400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr18:11884000-11893800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr18:11884000-11893800	Strong transcription	Duodenum Smooth Muscle	Duodenum
21	chr18:11884000-11894200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr18:11884000-11897000	Strong transcription	Skeletal Muscle Male	skeletal muscle
23	chr18:11884000-11897200	Strong transcription	Fetal Muscle Trunk	muscle
24	chr18:11884000-11898200	Strong transcription	Fetal Muscle Leg	muscle
25	chr18:11884000-11898800	Strong transcription	Thymus	Thymus
26	chr18:11884000-11899800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr18:11884000-11906200	Strong transcription	Fetal Thymus	thymus
28	chr18:11884200-11893600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr18:11884200-11897000	Strong transcription	Dnd41	blood
30	chr18:11884600-11894000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
31	chr18:11885000-11894200	Strong transcription	Spleen	Spleen
32	chr18:11885000-11905400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
33	chr18:11885400-11907000	Weak transcription	HMEC	breast
34	chr18:11885600-11905800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
35	chr18:11885600-11907400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr18:11885800-11893400	Strong transcription	Primary B cells from peripheral blood	blood
37	chr18:11885800-11895000	Weak transcription	Muscle Satellite Cultured Cells	--
38	chr18:11886000-11893600	Strong transcription	Liver	Liver
39	chr18:11886600-11903200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
40	chr18:11886600-11906200	Weak transcription	Fetal Kidney	kidney
41	chr18:11886800-11902200	Weak transcription	H1 Cell Line	embryonic stem cell
42	chr18:11886800-11902400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
43	chr18:11887000-11895000	Weak transcription	Fetal Brain Female	brain
44	chr18:11887000-11895600	Weak transcription	NHLF	lung
45	chr18:11887000-11902200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr18:11887200-11902600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr18:11887200-11902800	Weak transcription	HSMMtube	muscle
48	chr18:11888000-11905600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
49	chr18:11888000-11907200	Weak transcription	HSMM	muscle
50	chr18:11888200-11893800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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