Variant report

Variant	nsv898055
Chromosome Location	chr11:85968623-86000757
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:614)
CpG islands
(count:183)
Chromatin interactive
region (count:47)
LncRNA
region (count:4)
Mature miRNA
region (count: 2)
miRNA target
sites (count:5)

(count:614 , 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	ATF2	chr11:85997961-85998737	GM12878	blood:	n/a	n/a
2	ATF2	chr11:85997915-85998761	GM12878	blood:	n/a	n/a
3	BACH1	chr11:85990343-85990380	K562	blood:	n/a	n/a
4	BATF	chr11:85998063-85998725	GM12878	blood:	n/a	chr11:85998410-85998419
5	BATF	chr11:85998112-85998575	GM12878	blood:	n/a	chr11:85998410-85998419
6	BCL11A	chr11:85998142-85998534	GM12878	blood:	n/a	chr11:85998384-85998393
7	BCL11A	chr11:85998048-85998678	GM12878	blood:	n/a	chr11:85998384-85998393
8	BCL3	chr11:85998176-85998475	GM12878	blood:	n/a	chr11:85998384-85998393
9	BCL3	chr11:85997969-85998624	GM12878	blood:	n/a	chr11:85998384-85998393
10	BCLAF1	chr11:85997965-85998736	GM12878	blood:	n/a	chr11:85998384-85998393
11	BCLAF1	chr11:85998094-85998651	GM12878	blood:	n/a	chr11:85998384-85998393
12	CBX3	chr11:85999784-86000228	K562	blood:	n/a	n/a
13	CEBPB	chr11:85998134-85998334	A549	lung:	n/a	chr11:85998179-85998190
14	CEBPB	chr11:85988907-85989071	K562	blood:	n/a	n/a
15	CEBPB	chr11:85997894-85998789	GM12878	blood:	n/a	chr11:85998726-85998737 chr11:85998179-85998190 chr11:85998726-85998737
16	CEBPB	chr11:86000585-86000930	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr11:86000720-86000821	A549	lung:	n/a	n/a
18	CEBPB	chr11:85998722-85998831	K562	blood:	n/a	chr11:85998726-85998737 chr11:85998802-85998813 chr11:85998726-85998737
19	CEBPB	chr11:85998062-85998268	HepG2	liver:	n/a	chr11:85998179-85998190
20	CEBPB	chr11:85998758-85998833	HepG2	liver:	n/a	chr11:85998802-85998813
21	CEBPB	chr11:86000587-86000916	IMR90	lung:	n/a	n/a
22	CREB1	chr11:85998006-85998754	GM12878	blood:	n/a	n/a
23	CTCF	chr11:85972500-85972650	GM12872	blood:	n/a	n/a
24	CTCF	chr11:85985700-85985850	HL-60	blood:	n/a	n/a
25	CTCF	chr11:85987026-85987098	HepG2	liver:	n/a	n/a
26	CTCF	chr11:85986980-85987130	HRE	kidney:	n/a	n/a
27	CTCF	chr11:85985473-85986061	A549	lung:	n/a	n/a
28	CTCF	chr11:85972492-85972643	MCF-7	breast:	n/a	n/a
29	CTCF	chr11:85985640-85985790	HFF-Myc	foreskin:	n/a	n/a
30	CTCF	chr11:85987020-85987170	MCF-7	breast:	n/a	n/a
31	CTCF	chr11:85972486-85972682	MCF-7	breast:	n/a	n/a
32	CTCF	chr11:85985660-85985810	AG04449	skin:	n/a	n/a
33	CTCF	chr11:85985660-85985810	HBMEC	blood vessel:	n/a	n/a
34	CTCF	chr11:85972420-85972570	A549	lung:	n/a	n/a
35	CTCF	chr11:85987000-85987150	HMEC	breast:	n/a	n/a
36	CTCF	chr11:85985620-85985770	GM12865	blood:	n/a	n/a
37	CTCF	chr11:85980980-85981130	MCF-7	breast:	n/a	n/a
38	CTCF	chr11:85985700-85985850	MCF-7	breast:	n/a	n/a
39	CTCF	chr11:85972550-85972636	HepG2	liver:	n/a	n/a
40	CTCF	chr11:85972525-85972610	GM19238	blood:	n/a	n/a
41	CTCF	chr11:85985840-85985990	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr11:85985620-85985770	HRPEpiC	eye:	n/a	n/a
43	CTCF	chr11:85985660-85985810	GM12875	blood:	n/a	n/a
44	CTCF	chr11:85986900-85987050	GM12865	blood:	n/a	n/a
45	CTCF	chr11:85972500-85972650	GM12873	blood:	n/a	n/a
46	CTCF	chr11:85985485-85985921	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr11:85985580-85985730	SAEC	small airway:	n/a	n/a
48	CTCF	chr11:85985620-85985770	GM12878	blood:	n/a	n/a
49	CTCF	chr11:85985700-85985850	HEEpiC	esophagus:	n/a	n/a
50	CTCF	chr11:85987000-85987150	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:85995223-85995273	GM06990	blood:	n/a
2	chr11:85995223-85995273	MCF10A-Er-Src	breast:	n/a
3	chr11:85995039-85995089	HIPEpiC	eye:	n/a
4	chr11:85995223-85995273	H1-hESC	embryonic stem cell:	embryo
5	chr11:85995039-85995089	NB4	blood:	n/a
6	chr11:85995039-85995089	AoSMC	blood vessel:	n/a
7	chr11:85995223-85995273	HEEpiC	esophagus:	n/a
8	chr11:85989647-85989697	ovcar-3	ovarian:	n/a
9	chr11:85989647-85989697	HNPCEpiC	eye:	n/a
10	chr11:85995223-85995273	Hepatocyte	liver:	n/a
11	chr11:85989647-85989697	K562	blood:	n/a
12	chr11:85995223-85995273	IMR90	lung:	fetal
13	chr11:85995223-85995273	A549	lung:	n/a
14	chr11:85995039-85995089	GM12891	blood:	n/a
15	chr11:85995039-85995089	A549	lung:	n/a
16	chr11:85989647-85989697	SK-N-MC	brain:	n/a
17	chr11:85995039-85995089	PrEC	prostate:	n/a
18	chr11:85995223-85995273	HCF	heart:	n/a
19	chr11:85995223-85995273	NH-A	brain:	n/a
20	chr11:85995039-85995089	SKMC	muscle:	n/a
21	chr11:85995223-85995273	CMK	blood:	n/a
22	chr11:85995039-85995089	BE2_C	brain:	n/a
23	chr11:85989647-85989697	ProgFib	skin:	n/a
24	chr11:85989647-85989697	GM12892	blood:	n/a
25	chr11:85995223-85995273	ProgFib	skin:	n/a
26	chr11:85995039-85995089	H1-hESC	embryonic stem cell:	embryo
27	chr11:85989647-85989697	GM12891	blood:	n/a
28	chr11:85995039-85995089	HCPEpiC	choroid plexus:	n/a
29	chr11:85995039-85995089	ECC-1	luminal epithelium:	n/a
30	chr11:85989647-85989697	HL-60	blood:	n/a
31	chr11:85995039-85995089	HPAEpiC	pulmonary alveolar:	n/a
32	chr11:85995039-85995089	PANC-1	pancreas:	n/a
33	chr11:85995223-85995273	RPTEC	kidney:	n/a
34	chr11:85995039-85995089	HCF	heart:	n/a
35	chr11:85989647-85989697	H1-hESC	embryonic stem cell:	embryo
36	chr11:85989647-85989697	ECC-1	luminal epithelium:	n/a
37	chr11:85995223-85995273	HIPEpiC	eye:	n/a
38	chr11:85989647-85989697	SK-N-SH_RA	brain:	n/a
39	chr11:85989647-85989697	AG09319	gingival:	n/a
40	chr11:85989647-85989697	HMEC	breast:	n/a
41	chr11:85989647-85989697	MCF10A-Er-Src	breast:	n/a
42	chr11:85995039-85995089	RPTEC	kidney:	n/a
43	chr11:85989647-85989697	CMK	blood:	n/a
44	chr11:85995039-85995089	HRCEpiC	kidney:	n/a
45	chr11:85995039-85995089	Caco-2	colon:	n/a
46	chr11:85989647-85989697	PrEC	prostate:	n/a
47	chr11:85995223-85995273	HRCEpiC	kidney:	n/a
48	chr11:85989647-85989697	IMR90	lung:	fetal
49	chr11:85989647-85989697	AoSMC	blood vessel:	n/a
50	chr11:85989647-85989697	HRPEpiC	eye:	n/a

(count:47 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:85954518..85956806-chr11:85983872..85987966,3	MCF-7	breast:
2	chr11:85971654..85973609-chr11:85974451..85977409,3	K562	blood:
3	chr11:85954989..85958031-chr11:85971224..85974076,3	MCF-7	breast:
4	chr11:85986570..85988252-chr11:85990111..85992290,2	MCF-7	breast:
5	chr11:85985327..85988221-chr11:85991640..85993778,2	K562	blood:
6	chr11:85965815..85967521-chr11:85980737..85982478,2	K562	blood:
7	chr11:85978505..85980119-chr11:86012077..86014955,2	K562	blood:
8	chr11:85977646..85979205-chr11:85985350..85987005,2	K562	blood:
9	chr11:85986924..85991339-chr11:85991702..85995217,5	K562	blood:
10	chr11:85652016..85653035-chr11:85985052..85986168,4	MCF-7	breast:
11	chr11:85999579..86001748-chr11:86010935..86013289,2	K562	blood:
12	chr11:85988589..85992349-chr11:86011811..86014715,3	MCF-7	breast:
13	chr11:85955083..85957897-chr11:85979233..85982027,2	K562	blood:
14	chr11:85993708..85996490-chr11:86003264..86007905,4	K562	blood:
15	chr11:85984064..85985604-chr11:85986241..85988908,2	K562	blood:
16	chr11:85961896..85964300-chr11:85972097..85973858,2	K562	blood:
17	chr11:85967614..85970637-chr11:85971235..85974775,4	K562	blood:
18	chr11:85990195..85992374-chr11:86002425..86005252,2	K562	blood:
19	chr11:85982147..85984996-chr11:85985369..85987583,3	MCF-7	breast:
20	chr11:85967614..85970637-chr11:85971235..85974775,4	K562	blood:
21	chr11:85984064..85986424-chr11:85987408..85989303,2	K562	blood:
22	chr11:85989760..85992310-chr11:86001977..86004661,2	MCF-7	breast:
23	chr11:85780153..85782337-chr11:85980633..85982185,2	K562	blood:
24	chr11:85974215..85977214-chr11:85984888..85986859,2	MCF-7	breast:
25	chr11:85954640..85957647-chr11:85979944..85983156,3	MCF-7	breast:
26	chr11:85967045..85968879-chr11:85987127..85988641,2	K562	blood:
27	chr11:85744986..85747847-chr11:85984634..85986736,2	K562	blood:
28	chr11:85996870..85999859-chr11:86001615..86003194,2	K562	blood:
29	chr11:85986924..85991339-chr11:85991702..85995217,5	K562	blood:
30	chr11:85954796..85956818-chr11:85983486..85986654,3	MCF-7	breast:
31	chr11:85970225..85973154-chr11:85973663..85975951,2	K562	blood:
32	chr11:85955876..85958194-chr11:85984411..85986234,2	K562	blood:
33	chr11:85992844..85996245-chr11:85997438..86001010,4	K562	blood:
34	chr11:85754219..85755757-chr11:85998190..86001098,2	K562	blood:
35	chr11:85953789..85956159-chr11:86000092..86002736,3	K562	blood:
36	chr11:85982331..85984866-chr11:86014885..86016908,2	MCF-7	breast:
37	chr11:85971469..85973576-chr11:86002289..86004505,2	MCF-7	breast:
38	chr11:85982247..85985107-chr11:85990925..85993009,2	K562	blood:
39	chr11:85752681..85753613-chr11:85986298..85987019,2	K562	blood:
40	chr11:85955961..85957578-chr11:85969257..85970806,2	K562	blood:
41	chr11:85968939..85971727-chr11:85976961..85979234,2	MCF-7	breast:
42	chr11:85988810..85991753-chr11:85992813..85995061,2	MCF-7	breast:
43	chr11:85966228..85969859-chr11:85975228..85979391,4	K562	blood:
44	chr11:85997706..86000207-chr11:86001867..86004535,3	MCF-7	breast:
45	chr11:85569234..85571636-chr11:85985144..85986966,2	K562	blood:
46	chr11:85990243..85992364-chr11:85993264..85996035,2	K562	blood:
47	chr11:85982247..85985107-chr11:85990925..85993009,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ME3-1	chr11:85996202-85997182	ENSG00000247264
2	lnc-ME3-1	chr11:85994954-85995893	ENSG00000247264
3	lnc-ME3-1	chr11:85997840-85998013	ENSG00000247264
4	lnc-EED-1	chr11:85994969-85995710	NONHSAT023463

miRNA name	Chromosome Location	mirBase accession
hsa-miR-6755-5p	chr11:85989380-85989401	MIMAT0027410
hsa-miR-6755-3p	chr11:85989419-85989440	MIMAT0027411

(count:5 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	EED	hsa-miR-30c-5p	chr11:85989688-85989711
2	EED	hsa-miR-101-3p	chr11:85989727-85989733
3	EED	hsa-miR-30c-5p	chr11:85989713-85989720
4	EED	hsa-miR-101-3p	chr11:85989714-85989734
5	EED	hsa-miR-30c-5p	chr11:85989704-85989711

Variant related genes	Relation type
EED	TF binding region
ENSG00000254783	TF binding region
EED	CpG island
ENSG00000254783	CpG island
ENSG00000073921	chromatin interactions
ENSG00000074266	chromatin interactions
ENSG00000149196	chromatin interactions
ENSG00000255222	chromatin interactions
ENSG00000254783	chromatin interactions
PSMD10	miRNA target sites
CTNNB1	miRNA target sites
PTEN	miRNA target sites

Extended variants
information (count: 1213 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:1213 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs974144	chr11:85968623-85968624	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs535645275	chr11:85968706-85968707	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs548967933	chr11:85968739-85968740	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs76565538	chr11:85968748-85968749	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs7931056	chr11:85968752-85968753	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs143091568	chr11:85968813-85968814	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs571703428	chr11:85968819-85968820	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs112749268	chr11:85968827-85968828	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs564471045	chr11:85968836-85968837	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs74567287	chr11:85968863-85968864	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs574103018	chr11:85968870-85968871	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs148228229	chr11:85968971-85968972	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs556543560	chr11:85968984-85968985	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs73511888	chr11:85969117-85969118	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs545320683	chr11:85969206-85969207	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs201614316	chr11:85969211-85969212	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs143977181	chr11:85969278-85969279	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs532802281	chr11:85969315-85969316	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs539905069	chr11:85969335-85969336	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs560204829	chr11:85969399-85969400	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs529047333	chr11:85969456-85969457	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs558270050	chr11:85969466-85969467	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs113366845	chr11:85969486-85969487	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs188812461	chr11:85969500-85969501	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs112331911	chr11:85969538-85969539	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs531622838	chr11:85969545-85969546	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs79829381	chr11:85969547-85969548	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs564848621	chr11:85969566-85969567	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs11234596	chr11:85969585-85969586	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs374812626	chr11:85969596-85969597	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs375324436	chr11:85969597-85969598	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs563888569	chr11:85969598-85969599	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs553933912	chr11:85969604-85969605	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs79585759	chr11:85969613-85969614	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs12293294	chr11:85969617-85969618	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs567763738	chr11:85969628-85969629	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs113127075	chr11:85969651-85969652	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs536416089	chr11:85969654-85969655	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs556694888	chr11:85969684-85969685	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs576262091	chr11:85969685-85969686	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs111795436	chr11:85969693-85969694	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs545285355	chr11:85969711-85969712	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs370473004	chr11:85969714-85969715	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs139347143	chr11:85969715-85969716	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs565623665	chr11:85969718-85969719	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs186094733	chr11:85969722-85969723	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs540242210	chr11:85969723-85969724	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs190617481	chr11:85969788-85969789	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs117394557	chr11:85969804-85969805	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs60150276	chr11:85969828-85969829	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	20729466	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	22429812	CNVD
Breast cancer	21364760	CNVD
Ovarian neoplasms	16753589	CNVD
Breast cancer	16608533	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Sudden cardiac death	19188705	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Ductal carcinoma	22052326	CNVD
Obesity	20622171	CNVD
small cell lung cancer	20016488	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Attention deficit hyperactivity disorder	22241247	CNVD
Breast cancer	21958427	CNVD
Breast cancer	17133270	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:989 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:85957200-85972400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr11:85957200-85972400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr11:85957200-85972400	Weak transcription	Esophagus	oesophagus
4	chr11:85957200-85995400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr11:85957400-85985600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr11:85957400-86008000	Weak transcription	Psoas Muscle	Psoas
7	chr11:85957800-85997200	Weak transcription	Colonic Mucosa	Colon
8	chr11:85957800-85999800	Weak transcription	Brain Cingulate Gyrus	brain
9	chr11:85958400-85972400	Weak transcription	Aorta	Aorta
10	chr11:85958400-85997200	Weak transcription	Brain Germinal Matrix	brain
11	chr11:85959200-85974000	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr11:85959200-85988000	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr11:85959200-85988600	Weak transcription	Brain Angular Gyrus	brain
14	chr11:85959200-85997600	Weak transcription	Colon Smooth Muscle	Colon
15	chr11:85959400-85995000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
16	chr11:85960000-85970800	Weak transcription	Fetal Brain Female	brain
17	chr11:85960000-85972400	Weak transcription	Pancreas	Pancrea
18	chr11:85960200-85972800	Weak transcription	Skeletal Muscle Female	skeletal muscle
19	chr11:85960200-85985600	Weak transcription	Gastric	stomach
20	chr11:85960600-85972200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr11:85960800-85972400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr11:85960800-85988000	Weak transcription	Fetal Heart	heart
23	chr11:85961000-85972200	Weak transcription	Ovary	ovary
24	chr11:85961000-85972400	Weak transcription	Right Ventricle	heart
25	chr11:85961000-85996000	Strong transcription	Monocytes-CD14+_RO01746	blood
26	chr11:85961000-85997000	Weak transcription	Stomach Mucosa	stomach
27	chr11:85961200-85972600	Weak transcription	NHEK	skin
28	chr11:85961400-85980600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr11:85961400-85985800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr11:85961600-85970600	Weak transcription	A549	lung
31	chr11:85961600-85972400	Weak transcription	Small Intestine	intestine
32	chr11:85961600-85974400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
33	chr11:85961600-85998000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
34	chr11:85961800-85972400	Weak transcription	NHLF	lung
35	chr11:85961800-85988000	Weak transcription	Brain Substantia Nigra	brain
36	chr11:85962800-85969600	Strong transcription	Hela-S3	cervix
37	chr11:85962800-85972400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr11:85962800-85975200	Weak transcription	NHDF-Ad	bronchial
39	chr11:85963000-85984400	Weak transcription	Pancreatic Islets	Pancreatic Islet
40	chr11:85963800-85970800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr11:85964000-85972400	Weak transcription	Lung	lung
42	chr11:85964000-85995000	Weak transcription	H9 Cell Line	embryonic stem cell
43	chr11:85964200-85969600	Weak transcription	Fetal Stomach	stomach
44	chr11:85964200-85972400	Weak transcription	Spleen	Spleen
45	chr11:85964400-85980000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
46	chr11:85964400-85987600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
47	chr11:85965400-85969200	Strong transcription	Primary T helper cells PMA-I stimulated	--
48	chr11:85965800-85969200	Strong transcription	K562	blood
49	chr11:85965800-85975400	Strong transcription	Primary T cells fromperipheralblood	blood
50	chr11:85965800-85976400	Strong transcription	Breast Myoepithelial Primary Cells	Breast

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