Variant report

Variant	nsv898419
Chromosome Location	chr11:119488646-119518006
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CHD2	chr11:119497773-119497813	GM12878	blood:	n/a	n/a
2	CTCF	chr11:119494920-119495070	GM12867	blood:	n/a	chr11:119494980-119495001 chr11:119494978-119494996 chr11:119494981-119494990 chr11:119494981-119494994
3	CTCF	chr11:119512800-119512950	HPF	lung:	n/a	chr11:119512917-119512938 chr11:119512918-119512931 chr11:119512918-119512927 chr11:119512916-119512932 chr11:119512915-119512933
4	CTCF	chr11:119495160-119495310	GM12872	blood:	n/a	n/a
5	CTCF	chr11:119512860-119513010	AG04450	lung:	n/a	chr11:119512917-119512938 chr11:119512918-119512931 chr11:119512918-119512927 chr11:119512916-119512932 chr11:119512915-119512933
6	CTCF	chr11:119512820-119512970	GM12871	blood:	n/a	chr11:119512917-119512938 chr11:119512918-119512931 chr11:119512918-119512927 chr11:119512916-119512932 chr11:119512915-119512933
7	CTCF	chr11:119503982-119504242	H1-hESC	embryonic stem cell:	n/a	n/a
8	CTCF	chr11:119495480-119495630	SAEC	small airway:	n/a	n/a
9	CTCF	chr11:119495440-119495590	K562	blood:	n/a	n/a
10	CTCF	chr11:119512670-119513050	K562	blood:	n/a	chr11:119512917-119512938 chr11:119512918-119512931 chr11:119512918-119512927 chr11:119512916-119512932 chr11:119512915-119512933
11	CTCF	chr11:119495080-119495230	AG10803	skin:	n/a	n/a
12	CTCF	chr11:119512839-119513011	ECC-1	luminal epithelium:	n/a	chr11:119512917-119512938 chr11:119512918-119512931 chr11:119512918-119512927 chr11:119512916-119512932 chr11:119512915-119512933
13	CTCF	chr11:119494856-119495092	LNCaP	prostate:	n/a	chr11:119494980-119495001 chr11:119494978-119494996 chr11:119494981-119494990 chr11:119494981-119494994
14	CTCF	chr11:119494900-119495050	GM12873	blood:	n/a	chr11:119494980-119495001 chr11:119494978-119494996 chr11:119494981-119494990 chr11:119494981-119494994
15	CTCF	chr11:119512823-119512990	GM13976	blood:	n/a	chr11:119512917-119512938 chr11:119512918-119512931 chr11:119512918-119512927 chr11:119512916-119512932 chr11:119512915-119512933
16	CTCF	chr11:119495180-119495330	HVMF	connective:	n/a	n/a
17	CTCF	chr11:119495040-119495190	HMF	breast:	n/a	n/a
18	CTCF	chr11:119508460-119508610	Hela-S3	cervix:	n/a	chr11:119508518-119508531
19	CTCF	chr11:119512776-119513034	LNCaP	prostate:	n/a	chr11:119512917-119512938 chr11:119512918-119512931 chr11:119512918-119512927 chr11:119512916-119512932 chr11:119512915-119512933
20	CTCF	chr11:119512840-119512990	GM12866	blood:	n/a	chr11:119512917-119512938 chr11:119512918-119512931 chr11:119512918-119512927 chr11:119512916-119512932 chr11:119512915-119512933
21	CTCF	chr11:119512860-119513010	HEK293	kidney:	n/a	chr11:119512917-119512938 chr11:119512918-119512931 chr11:119512918-119512927 chr11:119512916-119512932 chr11:119512915-119512933
22	CTCF	chr11:119512754-119513065	GM19240	blood:	n/a	chr11:119512917-119512938 chr11:119512918-119512931 chr11:119512918-119512927 chr11:119512916-119512932 chr11:119512915-119512933
23	CTCF	chr11:119512900-119513050	BE2_C	brain:	n/a	chr11:119512917-119512938 chr11:119512918-119512931 chr11:119512918-119512927 chr11:119512916-119512932 chr11:119512915-119512933
24	CTCF	chr11:119494846-119495076	MCF-7	breast:	n/a	chr11:119494980-119495001 chr11:119494978-119494996 chr11:119494981-119494990 chr11:119494981-119494994
25	CTCF	chr11:119504100-119504250	BE2_C	brain:	n/a	n/a
26	CTCF	chr11:119494900-119495050	GM12870	blood:	n/a	chr11:119494980-119495001 chr11:119494978-119494996 chr11:119494981-119494990 chr11:119494981-119494994
27	CTCF	chr11:119512775-119513045	A549	lung:	n/a	chr11:119512917-119512938 chr11:119512918-119512931 chr11:119512918-119512927 chr11:119512916-119512932 chr11:119512915-119512933
28	CTCF	chr11:119512700-119512850	GM12868	blood:	n/a	n/a
29	CTCF	chr11:119512840-119512990	HCFaa	heart:	n/a	chr11:119512917-119512938 chr11:119512918-119512931 chr11:119512918-119512927 chr11:119512916-119512932 chr11:119512915-119512933
30	CTCF	chr11:119494860-119495010	GM12872	blood:	n/a	chr11:119494980-119495001 chr11:119494978-119494996 chr11:119494981-119494990 chr11:119494981-119494994
31	CTCF	chr11:119495383-119495565	K562	blood:	n/a	n/a
32	CTCF	chr11:119495480-119495630	GM12864	blood:	n/a	n/a
33	CTCF	chr11:119494880-119495030	GM12869	blood:	n/a	chr11:119494980-119495001 chr11:119494978-119494996 chr11:119494981-119494990 chr11:119494981-119494994
34	CTCF	chr11:119512920-119513070	HFF-Myc	foreskin:	n/a	n/a
35	CTCF	chr11:119494880-119495030	GM12874	blood:	n/a	chr11:119494980-119495001 chr11:119494978-119494996 chr11:119494981-119494990 chr11:119494981-119494994
36	CTCF	chr11:119494960-119495110	GM12872	blood:	n/a	chr11:119494980-119495001 chr11:119494978-119494996 chr11:119494981-119494990 chr11:119494981-119494994
37	CTCF	chr11:119512796-119513045	MCF-7	breast:	n/a	chr11:119512917-119512938 chr11:119512918-119512931 chr11:119512918-119512927 chr11:119512916-119512932 chr11:119512915-119512933
38	CTCF	chr11:119493560-119493710	HBMEC	blood vessel:	n/a	chr11:119493619-119493632 chr11:119493616-119493634
39	CTCF	chr11:119504020-119504170	BE2_C	brain:	n/a	n/a
40	CTCF	chr11:119494646-119494770	K562	blood:	n/a	n/a
41	CTCF	chr11:119512820-119512970	GM12872	blood:	n/a	chr11:119512917-119512938 chr11:119512918-119512931 chr11:119512918-119512927 chr11:119512916-119512932 chr11:119512915-119512933
42	CTCF	chr11:119512753-119513039	HepG2	liver:	n/a	chr11:119512917-119512938 chr11:119512918-119512931 chr11:119512918-119512927 chr11:119512916-119512932 chr11:119512915-119512933
43	CTCF	chr11:119512820-119512970	WERI-Rb-1	eye:	n/a	chr11:119512917-119512938 chr11:119512918-119512931 chr11:119512918-119512927 chr11:119512916-119512932 chr11:119512915-119512933
44	CTCF	chr11:119513260-119513410	BE2_C	brain:	n/a	chr11:119513276-119513294
45	CTCF	chr11:119495700-119495850	GM12871	blood:	n/a	n/a
46	CTCF	chr11:119494900-119495050	WI-38	lung:	n/a	chr11:119494980-119495001 chr11:119494978-119494996 chr11:119494981-119494990 chr11:119494981-119494994
47	CTCF	chr11:119512880-119513030	HBMEC	blood vessel:	n/a	chr11:119512917-119512938 chr11:119512918-119512931 chr11:119512918-119512927 chr11:119512916-119512932 chr11:119512915-119512933
48	CTCF	chr11:119494860-119495010	BE2_C	brain:	n/a	chr11:119494980-119495001 chr11:119494978-119494996 chr11:119494981-119494990 chr11:119494981-119494994
49	CTCF	chr11:119495460-119495610	NB4	blood:	n/a	n/a
50	CTCF	chr11:119494820-119494970	AG10803	skin:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:119510240-119510290	SK-N-SH_RA	brain:	n/a
2	chr11:119510240-119510290	MCF10A-Er-Src	breast:	n/a
3	chr11:119510240-119510290	ovcar-3	ovarian:	n/a
4	chr11:119510240-119510290	BJ	skin:	n/a
5	chr11:119510240-119510290	SK-N-SH	brain:	n/a
6	chr11:119510240-119510290	PFSK-1	brain:	n/a
7	chr11:119510240-119510290	GM12892	blood:	n/a
8	chr11:119510240-119510290	MCF-7	breast:	n/a
9	chr11:119510240-119510290	HNPCEpiC	eye:	n/a
10	chr11:119510240-119510290	HRCEpiC	kidney:	n/a
11	chr11:119510240-119510290	A549	lung:	n/a
12	chr11:119510240-119510290	NT2-D1	testis:	n/a
13	chr11:119510240-119510290	HEEpiC	esophagus:	n/a
14	chr11:119510240-119510290	Jurkat	blood:	n/a
15	chr11:119510240-119510290	HCPEpiC	choroid plexus:	n/a
16	chr11:119510240-119510290	HRPEpiC	eye:	n/a
17	chr11:119510240-119510290	HPAEpiC	pulmonary alveolar:	n/a
18	chr11:119510240-119510290	GM12878	blood:	n/a
19	chr11:119510240-119510290	BE2_C	brain:	n/a
20	chr11:119510240-119510290	NHDF-neo	bronchial:	n/a
21	chr11:119510240-119510290	AG09319	gingival:	n/a
22	chr11:119510240-119510290	HRE	kidney:	n/a
23	chr11:119510240-119510290	GM12891	blood:	n/a
24	chr11:119510240-119510290	T-47D	breast:	n/a
25	chr11:119510240-119510290	ProgFib	skin:	n/a
26	chr11:119510240-119510290	HAEpiC	amniotic membrane:	n/a
27	chr11:119510240-119510290	CMK	blood:	n/a
28	chr11:119510240-119510290	GM06990	blood:	n/a
29	chr11:119510240-119510290	IMR90	lung:	fetal
30	chr11:119510240-119510290	AG10803	skin:	n/a
31	chr11:119510240-119510290	HCF	heart:	n/a
32	chr11:119510240-119510290	GM19239	blood:	n/a
33	chr11:119510240-119510290	HMEC	breast:	n/a
34	chr11:119510240-119510290	AG04450	lung:	fetal
35	chr11:119510240-119510290	ECC-1	luminal epithelium:	n/a
36	chr11:119510240-119510290	K562	blood:	n/a
37	chr11:119510240-119510290	Caco-2	colon:	n/a
38	chr11:119510240-119510290	SK-N-MC	brain:	n/a
39	chr11:119510240-119510290	HUVEC	blood vessel:	n/a
40	chr11:119510240-119510290	LNCaP	prostate:	n/a
41	chr11:119510240-119510290	SKMC	muscle:	n/a
42	chr11:119510240-119510290	PrEC	prostate:	n/a
43	chr11:119510240-119510290	RPTEC	kidney:	n/a
44	chr11:119510240-119510290	HL-60	blood:	n/a
45	chr11:119510240-119510290	H1-hESC	embryonic stem cell:	embryo
46	chr11:119510240-119510290	AG09309	skin:	n/a
47	chr11:119510240-119510290	NB4	blood:	n/a
48	chr11:119510240-119510290	HCM	heart:	n/a
49	chr11:119510240-119510290	Hepatocyte	liver:	n/a
50	chr11:119510240-119510290	PANC-1	pancreas:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:119352030..119353608-chr11:119494198..119496133,2	K562	blood:
2	chr11:119500808..119502957-chr11:119507140..119509263,2	MCF-7	breast:
3	chr11:119367442..119369349-chr11:119494053..119496718,2	K562	blood:
4	chr11:119513079..119515723-chr11:119516167..119519482,3	K562	blood:
5	chr11:119500808..119502957-chr11:119507140..119509263,2	MCF-7	breast:
6	chr11:119351812..119352603-chr11:119494941..119495456,2	K562	blood:
7	chr11:119498849..119500765-chr11:119521663..119523665,2	K562	blood:
8	chr11:119492357..119494104-chr11:119499707..119501476,2	MCF-7	breast:
9	chr11:119497063..119498948-chr11:119500859..119503017,2	K562	blood:
10	chr11:119512432..119513032-chr11:119599777..119600437,2	K562	blood:
11	chr1:156185738..156186265-chr11:119505514..119506034,2	MCF-7	breast:
12	chr11:119485457..119487077-chr11:119490067..119492945,2	K562	blood:
13	chr11:119351973..119352705-chr11:119512520..119513396,3	MCF-7	breast:
14	chr11:119506334..119509273-chr11:119511344..119513114,2	K562	blood:
15	chr11:119492357..119494104-chr11:119499707..119501476,2	MCF-7	breast:
16	chr11:119513079..119515723-chr11:119516167..119519482,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTD-2523D13.1.1-2	chr11:119507635-119507738	ENSG00000254561.2
2	lnc-CTD-2523D13.1.1-2	chr11:119502088-119502147	ENSG00000254561.2
3	lnc-CTD-2523D13.1.1-2	chr11:119507984-119508087	ENSG00000254561.1
4	lnc-PVRL1-2	chr11:119508844-119508910	NONHSAT024678
5	lnc-CTD-2523D13.1.1-2	chr11:119507635-119507738	ENSG00000254561.1
6	lnc-PVRL1-2	chr11:119499806-119499987	NONHSAT024678
7	lnc-CTD-2523D13.1.1-2	chr11:119510206-119513699	ENSG00000254561.1
8	lnc-PVRL1-2	chr11:119494120-119494459	NONHSAT024678
9	lnc-CTD-2523D13.1.1-2	chr11:119507984-119508087	ENSG00000254561.2
10	lnc-CTD-2523D13.1.1-2	chr11:119510206-119510327	ENSG00000254561.2
11	lnc-PVRL1-1	chr11:119488907-119489008	XLOC_009577
12	lnc-CTD-2523D13.1.1-2	chr11:119501959-119502147	ENSG00000254561.1
13	lnc-CTD-2523D13.1.1-2	chr11:119507643-119507738	NONHSAT024679

Variant related genes	Relation type
ENSG00000254561	TF binding region
PVRL1	TF binding region
ENSG00000254561	CpG island
PVRL1	CpG island
ENSG00000110400	chromatin interactions
ENSG00000254854	chromatin interactions
ENSG00000254561	chromatin interactions
NLRX1	miRNA target sites

Extended variants
information (count: 1300 )
Associated
traits (count: 111 )

Variant overlapped rSNPs/rCNVs (count:1300 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4499013	chr11:119488646-119488647	Enhancers Bivalent Enhancer Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs73578804	chr11:119488688-119488689	Enhancers Bivalent Enhancer Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs185452817	chr11:119488691-119488692	Enhancers Bivalent Enhancer Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs560228021	chr11:119488701-119488702	Enhancers Bivalent Enhancer Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs572350860	chr11:119488725-119488726	Enhancers Bivalent Enhancer Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs546166106	chr11:119488745-119488746	Enhancers Bivalent Enhancer Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs150765955	chr11:119488760-119488761	Enhancers Bivalent Enhancer Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs571673913	chr11:119488790-119488791	Enhancers Bivalent Enhancer Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs138099829	chr11:119488804-119488805	Enhancers Bivalent Enhancer Weak transcription Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs549952942	chr11:119488811-119488812	Enhancers Bivalent Enhancer Weak transcription Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs4354701	chr11:119488812-119488813	Enhancers Bivalent Enhancer Weak transcription Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs529422104	chr11:119488912-119488913	Enhancers Bivalent Enhancer Weak transcription Genic enhancers Flanking Active TSS Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
13	rs189475048	chr11:119488970-119488971	Enhancers Bivalent Enhancer Weak transcription Genic enhancers Flanking Active TSS Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
14	rs149527334	chr11:119489050-119489051	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs117039624	chr11:119489051-119489052	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs147459766	chr11:119489064-119489065	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs180727083	chr11:119489091-119489092	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs112930270	chr11:119489140-119489141	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs555945768	chr11:119489146-119489147	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs139820799	chr11:119489149-119489150	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs115683675	chr11:119489177-119489178	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs570719565	chr11:119489191-119489192	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs12361680	chr11:119489210-119489211	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs572112918	chr11:119489254-119489255	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs545823797	chr11:119489355-119489356	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs145347975	chr11:119489356-119489357	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs368904640	chr11:119489370-119489371	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs543235473	chr11:119489373-119489374	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs186055897	chr11:119489406-119489407	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs529365383	chr11:119489498-119489499	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs147282716	chr11:119489538-119489539	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs372242265	chr11:119489566-119489567	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs559427101	chr11:119489602-119489603	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs79544257	chr11:119489607-119489608	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs551381376	chr11:119489655-119489656	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs140797640	chr11:119489656-119489657	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs142417669	chr11:119489779-119489780	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs572172524	chr11:119489811-119489812	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs574491409	chr11:119489812-119489813	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs138713709	chr11:119489814-119489815	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs371885194	chr11:119489820-119489821	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs201106198	chr11:119489828-119489829	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs202136536	chr11:119489829-119489830	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs113404832	chr11:119489903-119489904	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs11217353	chr11:119489905-119489906	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs372510018	chr11:119489979-119489980	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs567898015	chr11:119489984-119489985	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs11217354	chr11:119490006-119490007	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs188862525	chr11:119490084-119490085	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs556682290	chr11:119490086-119490087	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:111)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	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
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	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
Cancer	22429812	CNVD
Breast cancer	16608533	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21364760	CNVD
Mental retardation	19966786	CNVD
Non-small cell lung cancer	21829676	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Ovarian cancer	21720365	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Neuroblastoma	17327916	CNVD
Malignant melanoma	17260012	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Renal cell carcinoma	21668985	CNVD
Developmental delay	21147756	CNVD
Emanuel syndrome	21549014	CNVD
Emanuel syndrome	18184694	CNVD
Non-syndromic sensorineural hearing loss	18184694	CNVD
Acute lymphoblastic leukemia	22581003	CNVD
Ovarian neoplasms	16753589	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cancer	21183584	CNVD
Retinoblastoma	22278416	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-syndromic sensorineural hearing loss	16829213	CNVD
Non-syndromic sensorineural hearing loss	16760666	CNVD
Squamous cell cancer	20885788	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Neurocytoma	17123091	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Central neurocytomas	17123091	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Hepatocellular carcinoma	16750200	CNVD
Multiple myeloma	17550852	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Acute myeloid leukemia	19651601	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	20409316	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Heart disease	20551144	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Breast cancer	17142309	CNVD
Autism	22543975	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	21509527	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:325 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:119485200-119489600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr11:119485400-119489800	Enhancers	HUVEC	blood vessel
3	chr11:119485400-119490400	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr11:119485600-119489000	Enhancers	Adipose Nuclei	Adipose
5	chr11:119485800-119488800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr11:119485800-119489000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr11:119485800-119489200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr11:119485800-119489400	Enhancers	NH-A	brain
9	chr11:119486200-119489200	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr11:119486400-119489000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr11:119486600-119489200	Enhancers	Placenta	Placenta
12	chr11:119486800-119489000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr11:119486800-119489200	Enhancers	Fetal Muscle Leg	muscle
14	chr11:119486800-119489400	Enhancers	HepG2	liver
15	chr11:119487000-119489200	Weak transcription	Primary hematopoietic stem cells	blood
16	chr11:119487200-119489000	Weak transcription	Stomach Mucosa	stomach
17	chr11:119487600-119489800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr11:119487800-119488800	Weak transcription	NHLF	lung
19	chr11:119487800-119489000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr11:119487800-119489000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr11:119487800-119489200	Flanking Active TSS	Brain Hippocampus Middle	brain
22	chr11:119487800-119489800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr11:119488000-119488800	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
24	chr11:119488000-119488800	Enhancers	Fetal Muscle Trunk	muscle
25	chr11:119488000-119488800	Enhancers	Lung	lung
26	chr11:119488000-119489000	Flanking Active TSS	Brain Angular Gyrus	brain
27	chr11:119488000-119489000	Flanking Active TSS	Brain Cingulate Gyrus	brain
28	chr11:119488000-119489200	Bivalent Enhancer	Fetal Lung	lung
29	chr11:119488000-119489400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr11:119488000-119489400	Enhancers	Cortex derived primary cultured neurospheres	brain
31	chr11:119488000-119489600	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr11:119488000-119489600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr11:119488200-119488800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr11:119488200-119489000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr11:119488200-119489000	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr11:119488200-119489000	Enhancers	Brain Germinal Matrix	brain
37	chr11:119488200-119489000	Flanking Active TSS	Brain Substantia Nigra	brain
38	chr11:119488200-119489400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
39	chr11:119488200-119489400	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr11:119488400-119488800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr11:119488400-119489000	Flanking Active TSS	Brain Anterior Caudate	brain
42	chr11:119488400-119489400	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr11:119488400-119489600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
44	chr11:119488600-119488800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
45	chr11:119488600-119488800	Enhancers	Right Atrium	heart
46	chr11:119488600-119489000	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr11:119488600-119489000	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
48	chr11:119488600-119494600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr11:119488800-119489000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
50	chr11:119488800-119489000	Active TSS	Brain Inferior Temporal Lobe	brain

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