Variant report

Variant	nsv897196
Chromosome Location	chr11:33106616-33152074
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:295)
CpG islands
(count:61)
Chromatin interactive
region (count:45)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:295 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr11:33111397-33111588	GM12878	blood:	n/a	chr11:33111512-33111523
2	CEBPB	chr11:33151957-33151985	HepG2	liver:	n/a	chr11:33151969-33151980
3	CEBPB	chr11:33129139-33129272	A549	lung:	n/a	n/a
4	CEBPB	chr11:33118742-33118790	Hela-S3	cervix:	n/a	chr11:33118768-33118779
5	CEBPB	chr11:33151916-33152063	H1-hESC	embryonic stem cell:	n/a	chr11:33151969-33151980
6	CEBPB	chr11:33118632-33118888	HepG2	liver:	n/a	chr11:33118768-33118779
7	CEBPB	chr11:33118617-33118929	K562	blood:	n/a	chr11:33118768-33118779
8	CEBPB	chr11:33115767-33116050	HepG2	liver:	n/a	chr11:33115900-33115911
9	CEBPB	chr11:33118688-33118870	H1-hESC	embryonic stem cell:	n/a	chr11:33118768-33118779
10	CEBPB	chr11:33118664-33118900	A549	lung:	n/a	chr11:33118768-33118779
11	CEBPB	chr11:33115744-33116039	IMR90	lung:	n/a	chr11:33115900-33115911
12	CEBPB	chr11:33138001-33138449	HCT-116	colon:	n/a	n/a
13	CEBPB	chr11:33115793-33116052	K562	blood:	n/a	chr11:33115900-33115911
14	CEBPB	chr11:33118504-33118972	A549	lung:	n/a	chr11:33118768-33118779
15	CEBPB	chr11:33151873-33152039	Hela-S3	cervix:	n/a	chr11:33151969-33151980
16	CEBPB	chr11:33118652-33118934	IMR90	lung:	n/a	chr11:33118768-33118779
17	CEBPB	chr11:33115758-33116018	A549	lung:	n/a	chr11:33115900-33115911
18	CEBPB	chr11:33143527-33143606	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr11:33111540-33111690	GM12870	blood:	n/a	n/a
20	CTCF	chr11:33111500-33111650	AoAF	blood vessel:	n/a	n/a
21	CTCF	chr11:33111480-33111630	GM12872	blood:	n/a	n/a
22	CTCF	chr11:33111439-33111645	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr11:33111500-33111650	Caco-2	colon:	n/a	n/a
24	CTCF	chr11:33107560-33107710	GM06990	blood:	n/a	n/a
25	CTCF	chr11:33111500-33111650	HPAF	blood vessel:	n/a	n/a
26	CTCF	chr11:33107580-33107730	Hela-S3	cervix:	n/a	chr11:33107709-33107727
27	CTCF	chr11:33111380-33111530	HEEpiC	esophagus:	n/a	n/a
28	CTCF	chr11:33111360-33111510	HAc	cerebellar:	n/a	n/a
29	CTCF	chr11:33111640-33111790	HEEpiC	esophagus:	n/a	n/a
30	CTCF	chr11:33111420-33111570	HFF-Myc	foreskin:	n/a	n/a
31	CTCF	chr11:33111480-33111630	NHDF-neo	bronchial:	n/a	n/a
32	CTCF	chr11:33111486-33111594	MCF-7	breast:	n/a	n/a
33	CTCF	chr11:33111520-33111670	AG10803	skin:	n/a	n/a
34	CTCF	chr11:33111480-33111630	HBMEC	blood vessel:	n/a	n/a
35	CTCF	chr11:33111500-33111650	HCFaa	heart:	n/a	n/a
36	CTCF	chr11:33111520-33111670	HEK293	kidney:	n/a	n/a
37	CTCF	chr11:33111480-33111630	GM12869	blood:	n/a	n/a
38	CTCF	chr11:33111439-33111677	GM12878	blood:	n/a	n/a
39	CTCF	chr11:33111680-33111830	HFF-Myc	foreskin:	n/a	n/a
40	CTCF	chr11:33107620-33107770	Caco-2	colon:	n/a	chr11:33107709-33107727
41	CTCF	chr11:33111360-33111510	NHLF	lung:	n/a	n/a
42	CTCF	chr11:33111520-33111670	HCM	heart:	n/a	n/a
43	CTCF	chr11:33111439-33111754	IMR90	lung:	n/a	n/a
44	CTCF	chr11:33111440-33111590	GM12878	blood:	n/a	n/a
45	CTCF	chr11:33111480-33111630	AG09319	gingival:	n/a	n/a
46	CTCF	chr11:33111512-33111655	HUVEC	blood vessel:	n/a	n/a
47	CTCF	chr11:33111460-33111610	AG09309	skin:	n/a	n/a
48	CTCF	chr11:33111440-33111590	HFF	foreskin:	n/a	n/a
49	CTCF	chr11:33111500-33111650	NHDF-neo	bronchial:	n/a	n/a
50	CTCF	chr11:33107685-33107728	MCF-7	breast:	n/a	chr11:33107709-33107727

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:33112779-33112829	MCF10A-Er-Src	breast:	n/a
2	chr11:33112779-33112829	Hela-S3	cervix:	n/a
3	chr11:33112779-33112829	HRE	kidney:	n/a
4	chr11:33112779-33112829	HL-60	blood:	n/a
5	chr11:33112779-33112829	IMR90	lung:	fetal
6	chr11:33112779-33112829	ovcar-3	ovarian:	n/a
7	chr11:33112779-33112829	HUVEC	blood vessel:	n/a
8	chr11:33112779-33112829	AoSMC	blood vessel:	n/a
9	chr11:33112779-33112829	BJ	skin:	n/a
10	chr11:33112779-33112829	SK-N-SH_RA	brain:	n/a
11	chr11:33112779-33112829	SAEC	small airway:	n/a
12	chr11:33112779-33112829	PrEC	prostate:	n/a
13	chr11:33112779-33112829	HCT-116	colon:	n/a
14	chr11:33112779-33112829	H1-hESC	embryonic stem cell:	embryo
15	chr11:33112779-33112829	NB4	blood:	n/a
16	chr11:33112779-33112829	PANC-1	pancreas:	n/a
17	chr11:33112779-33112829	GM06990	blood:	n/a
18	chr11:33112779-33112829	SKMC	muscle:	n/a
19	chr11:33112779-33112829	Jurkat	blood:	n/a
20	chr11:33112779-33112829	GM19239	blood:	n/a
21	chr11:33112779-33112829	NT2-D1	testis:	n/a
22	chr11:33112779-33112829	HCF	heart:	n/a
23	chr11:33112779-33112829	ECC-1	luminal epithelium:	n/a
24	chr11:33112779-33112829	PFSK-1	brain:	n/a
25	chr11:33112779-33112829	LNCaP	prostate:	n/a
26	chr11:33112779-33112829	HCPEpiC	choroid plexus:	n/a
27	chr11:33112779-33112829	RPTEC	kidney:	n/a
28	chr11:33112779-33112829	ProgFib	skin:	n/a
29	chr11:33112779-33112829	HMEC	breast:	n/a
30	chr11:33112779-33112829	SK-N-SH	brain:	n/a
31	chr11:33112779-33112829	HPAEpiC	pulmonary alveolar:	n/a
32	chr11:33112779-33112829	GM12878	blood:	n/a
33	chr11:33112779-33112829	NH-A	brain:	n/a
34	chr11:33112779-33112829	HCM	heart:	n/a
35	chr11:33112779-33112829	U87	brain:	n/a
36	chr11:33112779-33112829	CMK	blood:	n/a
37	chr11:33112779-33112829	HIPEpiC	eye:	n/a
38	chr11:33112779-33112829	HEK293	kidney:	embryo
39	chr11:33112779-33112829	NHDF-neo	bronchial:	n/a
40	chr11:33112779-33112829	MCF-7	breast:	n/a
41	chr11:33112779-33112829	Hepatocyte	liver:	n/a
42	chr11:33112779-33112829	AG09309	skin:	n/a
43	chr11:33112779-33112829	NHBE	bronchial:	n/a
44	chr11:33112779-33112829	HAEpiC	amniotic membrane:	n/a
45	chr11:33112779-33112829	A549	lung:	n/a
46	chr11:33112779-33112829	GM12891	blood:	n/a
47	chr11:33112779-33112829	BE2_C	brain:	n/a
48	chr11:33112779-33112829	K562	blood:	n/a
49	chr11:33112779-33112829	AG09319	gingival:	n/a
50	chr11:33112779-33112829	HRPEpiC	eye:	n/a

(count:45 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:33134443..33136526-chr11:33141059..33143030,2	K562	blood:
2	chr11:33147528..33150547-chr11:33179225..33184125,4	MCF-7	breast:
3	chr11:33060966..33062993-chr11:33105012..33106638,2	K562	blood:
4	chr11:33124155..33125831-chr11:33126964..33129155,2	K562	blood:
5	chr11:33124155..33125831-chr11:33126964..33129155,2	K562	blood:
6	chr11:33060175..33062354-chr11:33124123..33126610,2	MCF-7	breast:
7	chr11:33126663..33129359-chr11:33132478..33134732,2	K562	blood:
8	chr11:33097286..33101981-chr11:33104595..33108523,4	K562	blood:
9	chr11:33137241..33139373-chr11:33181195..33183827,2	K562	blood:
10	chr11:33115745..33117577-chr11:33119372..33121372,2	K562	blood:
11	chr11:33112203..33114352-chr11:33151243..33153695,2	K562	blood:
12	chr11:33139735..33146600-chr11:33146867..33150605,7	K562	blood:
13	chr11:33099184..33100700-chr11:33113434..33116285,2	MCF-7	breast:
14	chr11:33107195..33109428-chr11:33181962..33183514,2	K562	blood:
15	chr11:33133284..33135813-chr11:33138983..33141504,2	MCF-7	breast:
16	chr11:33120707..33123516-chr11:33278200..33280006,2	K562	blood:
17	chr11:33124274..33125831-chr11:33126964..33128928,2	K562	blood:
18	chr11:33138621..33140759-chr11:33141891..33144623,2	K562	blood:
19	chr11:33133284..33135813-chr11:33138983..33141504,2	MCF-7	breast:
20	chr11:33139857..33145009-chr11:33151477..33155774,5	K562	blood:
21	chr11:33124274..33125831-chr11:33126964..33128928,2	K562	blood:
22	chr11:33107993..33109639-chr11:33110999..33113012,2	K562	blood:
23	chr11:33134443..33136526-chr11:33141059..33143030,2	K562	blood:
24	chr11:33145023..33150108-chr11:33154363..33159467,8	K562	blood:
25	chr11:33118081..33120716-chr11:33128955..33131930,2	MCF-7	breast:
26	chr11:33146192..33148602-chr11:33177101..33179018,2	K562	blood:
27	chr11:33139735..33146600-chr11:33146867..33150605,7	K562	blood:
28	chr11:33149721..33151534-chr11:33161155..33165147,4	K562	blood:
29	chr11:33151982..33154507-chr11:33378792..33381624,2	K562	blood:
30	chr11:33146625..33149206-chr6:52859190..52861528,2	K562	blood:
31	chr11:33126663..33129359-chr11:33132478..33134732,2	K562	blood:
32	chr11:33144694..33146600-chr11:33148884..33151282,2	K562	blood:
33	chr11:33133887..33136865-chr11:33162527..33165170,2	K562	blood:
34	chr11:33118081..33120716-chr11:33128955..33131930,2	MCF-7	breast:
35	chr11:33138621..33140759-chr11:33141891..33144623,2	K562	blood:
36	chr11:33110539..33112969-chr11:33181775..33184270,2	MCF-7	breast:
37	chr11:33142839..33144510-chr11:33145083..33148009,2	MCF-7	breast:
38	chr11:33107993..33109639-chr11:33110999..33113012,2	K562	blood:
39	chr11:33144694..33146600-chr11:33148884..33151282,2	K562	blood:
40	chr11:33139857..33145009-chr11:33151477..33155774,5	K562	blood:
41	chr11:33131476..33135821-chr11:33137366..33139055,4	K562	blood:
42	chr11:33112203..33114352-chr11:33151243..33153695,2	K562	blood:
43	chr11:33115745..33117577-chr11:33119372..33121372,2	K562	blood:
44	chr11:33142839..33144510-chr11:33145083..33148009,2	MCF-7	breast:
45	chr11:33131476..33135821-chr11:33137366..33139055,4	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCDC73-5	chr11:33116283-33116906	expReg_chr11_2930_-

No data

Variant related genes	Relation type
CSTF3	TF binding region
CSTF3	CpG island
ENSG00000176102	chromatin interactions
ENSG00000176148	chromatin interactions
ENSG00000170899	chromatin interactions
ENSG00000202198	chromatin interactions
ENSG00000247151	chromatin interactions
ENSG00000213713	chromatin interactions
ENSG00000110422	chromatin interactions

Extended variants
information (count: 1368 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:1368 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3758741	chr11:33106616-33106617	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs377337032	chr11:33106623-33106624	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs372998614	chr11:33106630-33106631	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs377162271	chr11:33106674-33106675	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs370908432	chr11:33106690-33106691	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs551015961	chr11:33106724-33106725	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs149939387	chr11:33106738-33106739	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs35076726	chr11:33106765-33106766	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs200568543	chr11:33106774-33106775	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs145202125	chr11:33106801-33106802	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs200163537	chr11:33106859-33106860	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs143330290	chr11:33106867-33106868	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs369236108	chr11:33106872-33106873	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs200050515	chr11:33106903-33106904	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs140987237	chr11:33106907-33106908	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs61889307	chr11:33106908-33106909	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs71034648	chr11:33106913-33106914	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs147886653	chr11:33106914-33106915	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs145595659	chr11:33106915-33106916	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs573480815	chr11:33107096-33107097	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs10767987	chr11:33107102-33107103	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs190842129	chr11:33107190-33107191	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs183092700	chr11:33107206-33107207	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs376478270	chr11:33107220-33107221	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs543135667	chr11:33107221-33107222	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs370927014	chr11:33107345-33107346	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs373751924	chr11:33107364-33107365	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs369652270	chr11:33107382-33107383	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs367546306	chr11:33107396-33107397	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs371781850	chr11:33107434-33107435	Strong transcription Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs374097467	chr11:33107444-33107445	Strong transcription Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs367945525	chr11:33107486-33107487	Strong transcription Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs563376018	chr11:33107521-33107522	Strong transcription Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs116623504	chr11:33107564-33107565	Strong transcription Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs369970743	chr11:33107569-33107570	Strong transcription Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs373168530	chr11:33107571-33107572	Strong transcription Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs536921512	chr11:33107573-33107574	Strong transcription Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs545969010	chr11:33107637-33107638	Strong transcription Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs114705753	chr11:33107686-33107687	Strong transcription Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs10631653	chr11:33107692-33107693	Strong transcription Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs375678885	chr11:33107693-33107694	Strong transcription Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs397718693	chr11:33107694-33107695	Strong transcription Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs200947426	chr11:33107695-33107696	Strong transcription Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs145066590	chr11:33107806-33107807	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs7483391	chr11:33107821-33107822	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs148702976	chr11:33107833-33107834	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs371360392	chr11:33107850-33107851	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs552706192	chr11:33107885-33107886	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs200520542	chr11:33107932-33107933	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs4593981	chr11:33107977-33107978	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:79)

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

Chromatin state (count:957 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:33062800-33107400	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr11:33075000-33130200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr11:33076000-33129600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr11:33078200-33109000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
5	chr11:33078600-33109600	Strong transcription	Dnd41	blood
6	chr11:33079400-33110800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
7	chr11:33085200-33112000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
8	chr11:33085600-33107200	Weak transcription	K562	blood
9	chr11:33085600-33122000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
10	chr11:33086200-33122000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr11:33086400-33127400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr11:33086600-33119400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
13	chr11:33086800-33107800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr11:33087200-33109600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr11:33087200-33110800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr11:33087200-33113600	Strong transcription	Placenta	Placenta
17	chr11:33087200-33129400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr11:33087400-33107600	Strong transcription	Duodenum Mucosa	Duodenum
19	chr11:33087400-33108200	Strong transcription	Primary neutrophils fromperipheralblood	blood
20	chr11:33087400-33108800	Strong transcription	Primary monocytes fromperipheralblood	blood
21	chr11:33087400-33108800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr11:33087400-33109400	Strong transcription	Fetal Muscle Trunk	muscle
23	chr11:33087400-33109400	Strong transcription	Monocytes-CD14+_RO01746	blood
24	chr11:33087400-33109600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr11:33087400-33109800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr11:33087400-33109800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
27	chr11:33087600-33109600	Strong transcription	Primary T helper cells fromperipheralblood	blood
28	chr11:33087800-33111800	Strong transcription	A549	lung
29	chr11:33087800-33138000	Weak transcription	Stomach Mucosa	stomach
30	chr11:33089400-33113600	Strong transcription	Fetal Thymus	thymus
31	chr11:33094400-33117600	Weak transcription	Fetal Kidney	kidney
32	chr11:33094400-33121400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr11:33094600-33107200	Weak transcription	Fetal Heart	heart
34	chr11:33094800-33119400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
35	chr11:33095000-33126800	Weak transcription	Right Ventricle	heart
36	chr11:33095200-33119600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
37	chr11:33095400-33117400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
38	chr11:33097800-33117600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
39	chr11:33097800-33117800	Weak transcription	Hela-S3	cervix
40	chr11:33098000-33121400	Weak transcription	Small Intestine	intestine
41	chr11:33098000-33122600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
42	chr11:33098800-33127400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr11:33099000-33107000	Weak transcription	Colonic Mucosa	Colon
44	chr11:33099200-33107200	Weak transcription	NHEK	skin
45	chr11:33099200-33114000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr11:33099200-33129400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr11:33099400-33118800	Weak transcription	Skeletal Muscle Male	skeletal muscle
48	chr11:33100600-33107000	Weak transcription	Brain Angular Gyrus	brain
49	chr11:33100600-33121400	Weak transcription	Aorta	Aorta
50	chr11:33100800-33122000	Weak transcription	H9 Cell Line	embryonic stem cell

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