Variant report

Variant	nsv1047667
Chromosome Location	chr11:33119875-33301210
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3115)
CpG islands
(count:2325)
Chromatin interactive
region (count:187)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3115 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:33181198-33181511	K562	blood:	n/a	n/a
2	ARID3A	chr11:33279537-33280483	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:33204058-33204223	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:33280061-33280282	K562	blood:	n/a	n/a
5	ARID3A	chr11:33187666-33188187	K562	blood:	n/a	chr11:33188154-33188170
6	ARID3A	chr11:33182051-33183545	K562	blood:	n/a	n/a
7	ARID3A	chr11:33278760-33279150	HepG2	liver:	n/a	n/a
8	ARID3A	chr11:33280884-33281018	HepG2	liver:	n/a	n/a
9	ARID3A	chr11:33277822-33278022	HepG2	liver:	n/a	n/a
10	ARID3A	chr11:33182607-33183285	HepG2	liver:	n/a	n/a
11	ARID3A	chr11:33187786-33188158	HepG2	liver:	n/a	n/a
12	ARID3A	chr11:33233161-33233450	HepG2	liver:	n/a	n/a
13	ARID3A	chr11:33193183-33193188	K562	blood:	n/a	n/a
14	ARID3A	chr11:33280804-33281150	K562	blood:	n/a	n/a
15	ARID3A	chr11:33201178-33201210	K562	blood:	n/a	n/a
16	ARID3A	chr11:33169179-33169315	K562	blood:	n/a	n/a
17	ARID3A	chr11:33288174-33288395	K562	blood:	n/a	n/a
18	ARID3A	chr11:33229217-33229421	K562	blood:	n/a	n/a
19	ARID3A	chr11:33288039-33288460	HepG2	liver:	n/a	n/a
20	ATF1	chr11:33275258-33275288	K562	blood:	n/a	n/a
21	ATF1	chr11:33182918-33183497	K562	blood:	n/a	n/a
22	ATF1	chr11:33181115-33181435	K562	blood:	n/a	n/a
23	ATF1	chr11:33249480-33249846	K562	blood:	n/a	n/a
24	ATF1	chr11:33190481-33190793	K562	blood:	n/a	n/a
25	ATF2	chr11:33182750-33183468	GM12878	blood:	n/a	chr11:33183172-33183183
26	ATF2	chr11:33279439-33280494	GM12878	blood:	n/a	n/a
27	ATF2	chr11:33182564-33183612	H1-hESC	embryonic stem cell:	n/a	chr11:33183172-33183183
28	ATF2	chr11:33279927-33280370	H1-hESC	embryonic stem cell:	n/a	n/a
29	ATF2	chr11:33182677-33183409	GM12878	blood:	n/a	chr11:33183172-33183183
30	ATF2	chr11:33182565-33183521	H1-hESC	embryonic stem cell:	n/a	chr11:33183172-33183183
31	ATF3	chr11:33249491-33249809	K562	blood:	n/a	n/a
32	ATF3	chr11:33182813-33183435	K562	blood:	n/a	chr11:33183174-33183181 chr11:33183174-33183182 chr11:33183170-33183185 chr11:33183172-33183185 chr11:33183172-33183183 chr11:33183151-33183160 chr11:33183171-33183182
33	ATF3	chr11:33279599-33280413	A549	lung:	n/a	n/a
34	ATF3	chr11:33182601-33183715	A549	lung:	n/a	chr11:33183174-33183181 chr11:33183174-33183182 chr11:33183170-33183185 chr11:33183172-33183185 chr11:33183172-33183183 chr11:33183151-33183160 chr11:33183171-33183182
35	ATF3	chr11:33279487-33279990	A549	lung:	n/a	n/a
36	BACH1	chr11:33183058-33183405	K562	blood:	n/a	n/a
37	BACH1	chr11:33182721-33183535	H1-hESC	embryonic stem cell:	n/a	n/a
38	BACH1	chr11:33189975-33189977	K562	blood:	n/a	n/a
39	BACH1	chr11:33279271-33279281	H1-hESC	embryonic stem cell:	n/a	n/a
40	BACH1	chr11:33279652-33280280	H1-hESC	embryonic stem cell:	n/a	n/a
41	BCL3	chr11:33279715-33280657	A549	lung:	n/a	chr11:33280069-33280078 chr11:33280094-33280107 chr11:33280065-33280078 chr11:33280086-33280099 chr11:33280095-33280108
42	BCL3	chr11:33262786-33263061	GM12878	blood:	n/a	n/a
43	BCL3	chr11:33278860-33279547	A549	lung:	n/a	chr11:33279283-33279296 chr11:33279375-33279384
44	BCL3	chr11:33182611-33183511	A549	lung:	n/a	chr11:33183037-33183050
45	BCL3	chr11:33279580-33280476	A549	lung:	n/a	chr11:33280069-33280078 chr11:33280094-33280107 chr11:33280065-33280078 chr11:33280086-33280099 chr11:33280095-33280108
46	BCL3	chr11:33182479-33183467	A549	lung:	n/a	chr11:33183037-33183050
47	BCLAF1	chr11:33182620-33183480	K562	blood:	n/a	chr11:33183037-33183050
48	BCLAF1	chr11:33279558-33280680	K562	blood:	n/a	chr11:33280069-33280078 chr11:33280094-33280107 chr11:33280065-33280078 chr11:33280086-33280099 chr11:33280095-33280108
49	BCLAF1	chr11:33182707-33183496	K562	blood:	n/a	chr11:33183037-33183050
50	BCLAF1	chr11:33279496-33280164	GM12878	blood:	n/a	chr11:33280069-33280078 chr11:33280094-33280107 chr11:33280065-33280078 chr11:33280086-33280099 chr11:33280095-33280108

(count:2325 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:33183473-33183523	AoSMC	blood vessel:	n/a
2	chr11:33185376-33185426	HepG2	liver:	n/a
3	chr11:33183213-33183263	HNPCEpiC	eye:	n/a
4	chr11:33214297-33214347	Jurkat	blood:	n/a
5	chr11:33279087-33279137	ProgFib	skin:	n/a
6	chr11:33265440-33265490	BJ	skin:	n/a
7	chr11:33183110-33183160	Jurkat	blood:	n/a
8	chr11:33183473-33183523	AoSMC	blood vessel:	n/a
9	chr11:33185376-33185426	HepG2	liver:	n/a
10	chr11:33183213-33183263	HNPCEpiC	eye:	n/a
11	chr11:33214297-33214347	Jurkat	blood:	n/a
12	chr11:33279087-33279137	ProgFib	skin:	n/a
13	chr11:33265440-33265490	BJ	skin:	n/a
14	chr11:33183110-33183160	Jurkat	blood:	n/a
15	chr11:33183343-33183393	BE2_C	brain:	n/a
16	chr11:33183001-33183051	SKMC	muscle:	n/a
17	chr11:33209645-33209695	NT2-D1	testis:	n/a
18	chr11:33182890-33182940	HRE	kidney:	n/a
19	chr11:33265440-33265490	HUVEC	blood vessel:	n/a
20	chr11:33199839-33199889	HCPEpiC	choroid plexus:	n/a
21	chr11:33182799-33182849	HAEpiC	amniotic membrane:	n/a
22	chr11:33185376-33185426	AG09319	gingival:	n/a
23	chr11:33278679-33278729	HCM	heart:	n/a
24	chr11:33282841-33282891	AG09309	skin:	n/a
25	chr11:33279252-33279302	HPAEpiC	pulmonary alveolar:	n/a
26	chr11:33163286-33163336	Caco-2	colon:	n/a
27	chr11:33217195-33217245	SK-N-SH	brain:	n/a
28	chr11:33279136-33279186	GM12878	blood:	n/a
29	chr11:33209645-33209695	NB4	blood:	n/a
30	chr11:33278679-33278729	ovcar-3	ovarian:	n/a
31	chr11:33199839-33199889	HNPCEpiC	eye:	n/a
32	chr11:33279252-33279302	Hepatocyte	liver:	n/a
33	chr11:33183213-33183263	HRPEpiC	eye:	n/a
34	chr11:33279136-33279186	HRPEpiC	eye:	n/a
35	chr11:33199839-33199889	PFSK-1	brain:	n/a
36	chr11:33279252-33279302	CMK	blood:	n/a
37	chr11:33183473-33183523	NHBE	bronchial:	n/a
38	chr11:33265440-33265490	Hela-S3	cervix:	n/a
39	chr11:33278186-33278236	BE2_C	brain:	n/a
40	chr11:33182890-33182940	GM12878	blood:	n/a
41	chr11:33183110-33183160	CMK	blood:	n/a
42	chr11:33189542-33189592	LNCaP	prostate:	n/a
43	chr11:33183108-33183158	HCPEpiC	choroid plexus:	n/a
44	chr11:33279087-33279137	BJ	skin:	n/a
45	chr11:33183213-33183263	HMEC	breast:	n/a
46	chr11:33280012-33280062	HEK293	kidney:	embryo
47	chr11:33265440-33265490	HepG2	liver:	n/a
48	chr11:33182799-33182849	NHDF-neo	bronchial:	n/a
49	chr11:33182890-33182940	BJ	skin:	n/a
50	chr11:33279091-33279141	Jurkat	blood:	n/a

(count:187 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr11:33180418..33183694-chr11:33278346..33281012,5	MCF-7	breast:
2	chr11:33279524..33280025-chr3:9437578..9438488,2	Hela-S3	cervix:
3	chr11:33146192..33148602-chr11:33177101..33179018,2	K562	blood:
4	chr11:33165074..33167895-chr11:33168095..33170897,3	K562	blood:
5	chr11:33294153..33295925-chr11:33303597..33306470,2	MCF-7	breast:
6	chr11:33279534..33280463-chr2:39351094..39351986,2	Hela-S3	cervix:
7	chr11:33154713..33156915-chr11:33157694..33159800,2	MCF-7	breast:
8	chr11:33131476..33135821-chr11:33137366..33139055,4	K562	blood:
9	chr11:33182274..33183032-chr3:52007563..52008447,2	Hela-S3	cervix:
10	chr11:33278564..33280833-chr11:33295728..33298096,2	K562	blood:
11	chr11:33264545..33268685-chr11:33272682..33276323,4	MCF-7	breast:
12	chr11:32914066..32915835-chr11:33278115..33280779,2	K562	blood:
13	chr11:33124274..33125831-chr11:33126964..33128928,2	K562	blood:
14	chr11:33181954..33184910-chr11:33755905..33758961,3	K562	blood:
15	chr11:33180160..33185398-chr11:33277230..33283289,14	K562	blood:
16	chr11:33170533..33172129-chr11:33173815..33175713,2	MCF-7	breast:
17	chr11:33267480..33271185-chr11:33277468..33280694,5	MCF-7	breast:
18	chr11:33278424..33279208-chr12:46766017..46766703,2	NB4	blood:
19	chr11:33279068..33280061-chr11:67195914..67196832,2	Hela-S3	cervix:
20	chr11:33149721..33151534-chr11:33161155..33165147,4	K562	blood:
21	chr11:33277371..33280516-chr11:33349638..33353162,5	MCF-7	breast:
22	chr11:33151982..33154507-chr11:33378792..33381624,2	K562	blood:
23	chr11:33173832..33178118-chr11:33179757..33183730,5	MCF-7	breast:
24	chr11:33161983..33167383-chr11:33177368..33180644,5	K562	blood:
25	chr11:32914737..32917481-chr11:33177201..33180231,3	K562	blood:
26	chr11:33181707..33184014-chr11:33222885..33224416,2	K562	blood:
27	chr11:33265908..33267622-chr11:33278289..33281327,3	MCF-7	breast:
28	chr11:33139857..33145009-chr11:33151477..33155774,5	K562	blood:
29	chr11:33157006..33159275-chr11:33181412..33183264,2	K562	blood:
30	chr11:33262756..33265436-chr11:33277701..33280558,4	MCF-7	breast:
31	chr11:33144694..33146600-chr11:33148884..33151282,2	K562	blood:
32	chr11:33126663..33129359-chr11:33132478..33134732,2	K562	blood:
33	chr11:33198554..33200197-chr11:33279365..33281352,2	K562	blood:
34	chr11:33164604..33166371-chr11:33178493..33180493,2	MCF-7	breast:
35	chr11:33169593..33172505-chr11:33177595..33179412,2	K562	blood:
36	chr11:33279747..33280263-chrX:23801172..23801824,2	Hela-S3	cervix:
37	chr11:33278197..33279052-chr5:134240296..134240970,2	Hela-S3	cervix:
38	chr11:33277741..33279641-chr11:33288313..33289989,2	MCF-7	breast:
39	chr11:33154721..33157255-chr11:33279375..33281458,2	K562	blood:
40	chr11:33182326..33183217-chr11:33278148..33279535,3	Hela-S3	cervix:
41	chr10:74385851..74386629-chr11:33278605..33279285,2	Hela-S3	cervix:
42	chr11:33187786..33191779-chr11:33278023..33282064,7	MCF-7	breast:
43	chr11:33187508..33188019-chr11:33392733..33393351,2	MCF-7	breast:
44	chr11:32913171..32916144-chr11:33182605..33184521,3	K562	blood:
45	chr11:33182251..33184625-chr11:33185906..33187944,2	MCF-7	breast:
46	chr11:33277710..33282201-chr11:33292143..33296310,6	K562	blood:
47	chr11:33287096..33288603-chr11:33295589..33298178,2	K562	blood:
48	chr11:33137241..33139373-chr11:33181195..33183827,2	K562	blood:
49	chr11:33165074..33167895-chr11:33168095..33170897,3	K562	blood:
50	chr11:33284231..33286219-chr11:33288903..33290704,3	K562	blood:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TCP11L1-1	chr11:33210316-33210396	NONHSAT018691
2	lnc-CSTF3-5	chr11:33222131-33222464	NONHSAT018696
3	lnc-TCP11L1-1	chr11:33211479-33211840	ENSG00000247151
4	lnc-TCP11L1-1	chr11:33183234-33183327	ENSG00000247151
5	lnc-TCP11L1-1	chr11:33210316-33210396	ENSG00000247151
6	lnc-CSTF3-4	chr11:33212459-33213144	NONHSAT018694
7	lnc-TCP11L1-1	chr11:33183203-33183327	ENSG00000247151
8	lnc-TCP11L1-1	chr11:33211479-33213142	NONHSAT018691
9	lnc-CSTF3-3	chr11:33211608-33212049	NONHSAT018693
10	lnc-TCP11L1-1	chr11:33211479-33213144	ENSG00000247151
11	lnc-CSTF3-4	chr11:33212346-33212446	NONHSAT018694
12	lnc-TCP11L1-1	chr11:33210914-33211103	ENSG00000247151
13	lnc-TCP11L1-1	chr11:33210316-33210396	ENSG00000247151
14	lnc-TCP11L1-1	chr11:33210914-33211103	NONHSAT018691
15	lnc-TCP11L1-1	chr11:33183203-33183327	NONHSAT018691

No data

Variant related genes	Relation type
ENSG00000200485	TF binding region
CSTF3	TF binding region
ENSG00000241255	TF binding region
CSTF3-AS1	TF binding region
ENSG00000206808	TF binding region
HIPK3	TF binding region
RPL29P23	TF binding region
ENSG00000200485	CpG island
CSTF3	CpG island
ENSG00000241255	CpG island
CSTF3-AS1	CpG island
ENSG00000206808	CpG island
HIPK3	CpG island
RPL29P23	CpG island
ENSG00000110422	chromatin interactions
ENSG00000182718	chromatin interactions
ENSG00000128595	chromatin interactions
ENSG00000060749	chromatin interactions
ENSG00000141522	chromatin interactions
ENSG00000135387	chromatin interactions
ENSG00000114779	chromatin interactions
ENSG00000236778	chromatin interactions
ENSG00000260924	chromatin interactions
ENSG00000199568	chromatin interactions
ENSG00000207972	chromatin interactions
ENSG00000170899	chromatin interactions
ENSG00000196331	chromatin interactions
ENSG00000028528	chromatin interactions
ENSG00000176148	chromatin interactions
ENSG00000132570	chromatin interactions
ENSG00000115904	chromatin interactions
ENSG00000111669	chromatin interactions
ENSG00000105479	chromatin interactions
ENSG00000175634	chromatin interactions
ENSG00000200485	chromatin interactions
ENSG00000248487	chromatin interactions
ENSG00000108846	chromatin interactions
ENSG00000254718	chromatin interactions
ENSG00000263004	chromatin interactions
ENSG00000206808	chromatin interactions
ENSG00000107745	chromatin interactions
ENSG00000085063	chromatin interactions
ENSG00000247151	chromatin interactions
ENSG00000202198	chromatin interactions
ENSG00000079805	chromatin interactions
ENSG00000272762	chromatin interactions
ENSG00000117335	chromatin interactions
ENSG00000130066	chromatin interactions
ENSG00000177542	chromatin interactions
ENSG00000176102	chromatin interactions
ENSG00000102786	chromatin interactions
ENSG00000134294	chromatin interactions
ENSG00000206573	chromatin interactions
PSME3	miRNA target sites
ARID2	miRNA target sites
YWHAZ	miRNA target sites
ERI2	miRNA target sites
NUP160	miRNA target sites
MICALL1	miRNA target sites

Extended variants
information (count: 5952 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:5952 , 50 per page) page: 1 2 3 4 5 6 7 ... 120

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs544277409	chr11:33119920-33119921	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs564458843	chr11:33119938-33119939	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs577727457	chr11:33120014-33120015	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs146267790	chr11:33120038-33120039	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs560338822	chr11:33120058-33120059	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs185112396	chr11:33120064-33120065	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs189050383	chr11:33120099-33120100	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs563028661	chr11:33120108-33120109	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs530571469	chr11:33120143-33120144	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs35931906	chr11:33120260-33120261	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs200350025	chr11:33120265-33120266	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs181095002	chr11:33120280-33120281	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs184046143	chr11:33120310-33120311	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs546689227	chr11:33120338-33120339	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs566699700	chr11:33120424-33120425	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs201483492	chr11:33120527-33120528	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs143587013	chr11:33120531-33120532	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs369145220	chr11:33120554-33120555	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs550579722	chr11:33120566-33120567	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs555681844	chr11:33120627-33120628	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs199509103	chr11:33120713-33120714	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs201339713	chr11:33120721-33120722	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs377132192	chr11:33120739-33120740	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs577208868	chr11:33120777-33120778	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs111434204	chr11:33120837-33120838	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs538103891	chr11:33120844-33120845	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs557747463	chr11:33121018-33121019	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs188000615	chr11:33121025-33121026	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs577589096	chr11:33121034-33121035	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs529904471	chr11:33121064-33121065	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs540357825	chr11:33121103-33121104	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs200639777	chr11:33121121-33121122	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs573935089	chr11:33121136-33121137	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs377479942	chr11:33121144-33121145	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs542847234	chr11:33121147-33121148	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs78085398	chr11:33121166-33121167	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs531919563	chr11:33121253-33121254	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs369844451	chr11:33121285-33121286	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs200957450	chr11:33121294-33121295	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs111941014	chr11:33121444-33121445	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs552016351	chr11:33121472-33121473	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs564092793	chr11:33121481-33121482	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs532933776	chr11:33121490-33121491	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs567765847	chr11:33121525-33121526	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs10836022	chr11:33121582-33121583	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs66548785	chr11:33121605-33121606	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs548381436	chr11:33121630-33121631	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs535486640	chr11:33121631-33121632	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs180880796	chr11:33121668-33121669	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs7125136	chr11:33121669-33121670	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
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Medulloblastoma	16783165	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18194544	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21364760	CNVD
Glioblastoma multiforme	22286061	CNVD
Aniridia syndrome	21572526	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Retinoblastoma	22278416	CNVD
Denys-drash syndrome	21085971	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
WAGR syndrome	16773131	CNVD
Disorders of sex development	22290220	CNVD
Aniridia syndrome	17204608	CNVD
Mental retardation	17204608	CNVD
WAGR syndrome	19617690	CNVD
genitourinary abnormalities	17204608	CNVD
Breast cancer	16397240	CNVD
Mental retardation	16773131	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Cancer	21183584	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
WAGR syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Denys-drash syndrome	19566914	CNVD
Familial wilms tumor	19566914	CNVD
Frasier syndrome	19566914	CNVD
Non-small cell lung cancer	21829676	CNVD
WAGR syndrome	20603712	CNVD
Autism	17322880	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21858162	CNVD
Cancer	20164920	CNVD
Breast cancer	16620391	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:3993 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:33075000-33130200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr11:33076000-33129600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr11:33085600-33122000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr11:33086200-33122000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr11:33086400-33127400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr11:33087200-33129400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr11:33087800-33138000	Weak transcription	Stomach Mucosa	stomach
8	chr11:33094400-33121400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr11:33095000-33126800	Weak transcription	Right Ventricle	heart
10	chr11:33098000-33121400	Weak transcription	Small Intestine	intestine
11	chr11:33098000-33122600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr11:33098800-33127400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr11:33099200-33129400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr11:33100600-33121400	Weak transcription	Aorta	Aorta
15	chr11:33100800-33122000	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr11:33100800-33123800	Weak transcription	Fetal Brain Male	brain
17	chr11:33101600-33122400	Weak transcription	Esophagus	oesophagus
18	chr11:33103600-33128600	Weak transcription	Gastric	stomach
19	chr11:33104200-33128400	Weak transcription	Pancreas	Pancrea
20	chr11:33104800-33122600	Weak transcription	Spleen	Spleen
21	chr11:33104800-33133600	Weak transcription	Placenta Amnion	Placenta Amnion
22	chr11:33106800-33131600	Weak transcription	Psoas Muscle	Psoas
23	chr11:33107200-33121400	Weak transcription	Lung	lung
24	chr11:33107200-33124600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
25	chr11:33107600-33125600	Weak transcription	Rectal Smooth Muscle	rectum
26	chr11:33107600-33131200	Weak transcription	Fetal Heart	heart
27	chr11:33107800-33122000	Weak transcription	Brain Substantia Nigra	brain
28	chr11:33107800-33125400	Weak transcription	Colonic Mucosa	Colon
29	chr11:33107800-33131000	Weak transcription	Pancreatic Islets	Pancreatic Islet
30	chr11:33108200-33121400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr11:33108600-33122000	Weak transcription	Brain Cingulate Gyrus	brain
32	chr11:33109000-33122200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
33	chr11:33110400-33129800	Strong transcription	HUES64 Cell Line	embryonic stem cell
34	chr11:33110600-33121400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr11:33110800-33129400	Strong transcription	Monocytes-CD14+_RO01746	blood
36	chr11:33111000-33127200	Strong transcription	Dnd41	blood
37	chr11:33111200-33127600	Strong transcription	Primary monocytes fromperipheralblood	blood
38	chr11:33112000-33124600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr11:33113600-33161800	Weak transcription	Left Ventricle	heart
40	chr11:33114800-33128000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr11:33114800-33128600	Strong transcription	HUES48 Cell Line	embryonic stem cell
42	chr11:33115200-33123200	Strong transcription	Duodenum Mucosa	Duodenum
43	chr11:33115200-33129000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr11:33115600-33124400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
45	chr11:33115600-33124600	Strong transcription	Cortex derived primary cultured neurospheres	brain
46	chr11:33115600-33124800	Strong transcription	HUES6 Cell Line	embryonic stem cell
47	chr11:33115600-33126200	Strong transcription	Primary T helper cells fromperipheralblood	blood
48	chr11:33115600-33127400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr11:33115600-33127400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
50	chr11:33115600-33127400	Strong transcription	Placenta	Placenta

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