Variant report

Variant	nsv553447
Chromosome Location	chr11:8792622-8825966
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:440)
CpG islands
(count:307)
Chromatin interactive
region (count:25)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:440 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:8816236-8816720	HepG2	liver:	n/a	n/a
2	BCL11A	chr11:8799642-8799949	GM12878	blood:	n/a	n/a
3	BCL3	chr11:8797528-8797787	GM12878	blood:	n/a	chr11:8797577-8797586
4	BCL3	chr11:8797474-8797876	GM12878	blood:	n/a	chr11:8797577-8797586
5	BHLHE40	chr11:8799539-8799547	GM12878	blood:	n/a	n/a
6	BHLHE40	chr11:8797566-8797845	K562	blood:	n/a	n/a
7	BHLHE40	chr11:8807180-8807338	K562	blood:	n/a	n/a
8	BHLHE40	chr11:8816530-8816565	K562	blood:	n/a	n/a
9	BHLHE40	chr11:8806439-8806667	K562	blood:	n/a	n/a
10	BRCA1	chr11:8816704-8816706	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr11:8803274-8803465	K562	blood:	n/a	n/a
12	CEBPB	chr11:8814613-8815090	A549	lung:	n/a	chr11:8814866-8814877 chr11:8814810-8814821
13	CEBPB	chr11:8814649-8815051	K562	blood:	n/a	chr11:8814866-8814877 chr11:8814810-8814821
14	CEBPB	chr11:8816202-8816617	HepG2	liver:	n/a	n/a
15	CEBPB	chr11:8797786-8798132	HepG2	liver:	n/a	n/a
16	CEBPB	chr11:8802220-8802406	IMR90	lung:	n/a	chr11:8802287-8802298
17	CEBPB	chr11:8797772-8798153	HepG2	liver:	n/a	n/a
18	CEBPB	chr11:8814689-8815034	HepG2	liver:	n/a	chr11:8814866-8814877 chr11:8814810-8814821
19	CEBPB	chr11:8802138-8802399	K562	blood:	n/a	chr11:8802287-8802298
20	CEBPB	chr11:8802227-8802367	HepG2	liver:	n/a	chr11:8802287-8802298
21	CEBPB	chr11:8814679-8814962	Hela-S3	cervix:	n/a	chr11:8814866-8814877 chr11:8814810-8814821
22	CEBPB	chr11:8814671-8815044	A549	lung:	n/a	chr11:8814866-8814877 chr11:8814810-8814821
23	CEBPB	chr11:8814342-8815059	HepG2	liver:	n/a	chr11:8814866-8814877 chr11:8814810-8814821
24	CEBPB	chr11:8814767-8814986	K562	blood:	n/a	chr11:8814866-8814877 chr11:8814810-8814821
25	CEBPB	chr11:8814730-8814957	H1-hESC	embryonic stem cell:	n/a	chr11:8814866-8814877 chr11:8814810-8814821
26	CEBPB	chr11:8797911-8797987	K562	blood:	n/a	n/a
27	CEBPB	chr11:8814645-8815174	IMR90	lung:	n/a	chr11:8814866-8814877 chr11:8814810-8814821
28	CEBPB	chr11:8818635-8818761	A549	lung:	n/a	n/a
29	CEBPB	chr11:8814745-8814943	HepG2	liver:	n/a	chr11:8814866-8814877 chr11:8814810-8814821
30	CEBPB	chr11:8803289-8803489	IMR90	lung:	n/a	n/a
31	CEBPB	chr11:8814716-8814988	HepG2	liver:	n/a	chr11:8814866-8814877 chr11:8814810-8814821
32	CEBPD	chr11:8814754-8814979	HepG2	liver:	n/a	n/a
33	CHD1	chr11:8799511-8799605	GM12878	blood:	n/a	n/a
34	CHD2	chr11:8816492-8816686	HepG2	liver:	n/a	n/a
35	CHD2	chr11:8815873-8815969	HepG2	liver:	n/a	n/a
36	CTCF	chr11:8816452-8816637	MCF-7	breast:	n/a	chr11:8816539-8816552 chr11:8816540-8816549
37	CTCF	chr11:8816440-8816590	HepG2	liver:	n/a	chr11:8816539-8816552 chr11:8816540-8816549
38	CTCF	chr11:8816480-8816630	BJ	skin:	n/a	chr11:8816539-8816552 chr11:8816540-8816549
39	CTCF	chr11:8808600-8808750	HPAF	blood vessel:	n/a	n/a
40	CTCF	chr11:8808660-8808810	RPTEC	kidney:	n/a	n/a
41	CTCF	chr11:8816500-8816650	GM12867	blood:	n/a	chr11:8816539-8816552 chr11:8816540-8816549
42	CTCF	chr11:8816473-8816611	Kidney_OC	kidney:	n/a	chr11:8816539-8816552 chr11:8816540-8816549
43	CTCF	chr11:8803631-8803708	GM13976	blood:	n/a	n/a
44	CTCF	chr11:8816460-8816610	WI-38	lung:	n/a	chr11:8816539-8816552 chr11:8816540-8816549
45	CTCF	chr11:8816485-8816642	GM19240	blood:	n/a	chr11:8816539-8816552 chr11:8816540-8816549
46	CTCF	chr11:8816420-8816570	GM12873	blood:	n/a	chr11:8816539-8816552 chr11:8816540-8816549
47	CTCF	chr11:8808580-8808730	BJ	skin:	n/a	n/a
48	CTCF	chr11:8816324-8816646	H1-hESC	embryonic stem cell:	n/a	chr11:8816539-8816552 chr11:8816540-8816549
49	CTCF	chr11:8816480-8816630	HA-sp	spinal cord:	n/a	chr11:8816539-8816552 chr11:8816540-8816549
50	CTCF	chr11:8816520-8816670	Hela-S3	cervix:	n/a	chr11:8816539-8816552 chr11:8816540-8816549

(count:307 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:8793878-8793928	ProgFib	skin:	n/a
2	chr11:8821924-8821974	NT2-D1	testis:	n/a
3	chr11:8793878-8793928	ProgFib	skin:	n/a
4	chr11:8821924-8821974	NT2-D1	testis:	n/a
5	chr11:8793878-8793928	Hela-S3	cervix:	n/a
6	chr11:8793878-8793928	HEK293	kidney:	embryo
7	chr11:8808320-8808370	HepG2	liver:	n/a
8	chr11:8821924-8821974	PANC-1	pancreas:	n/a
9	chr11:8793878-8793928	ECC-1	luminal epithelium:	n/a
10	chr11:8793878-8793928	HCF	heart:	n/a
11	chr11:8821924-8821974	GM19239	blood:	n/a
12	chr11:8793878-8793928	HUVEC	blood vessel:	n/a
13	chr11:8800270-8800320	PrEC	prostate:	n/a
14	chr11:8816428-8816478	HCF	heart:	n/a
15	chr11:8821924-8821974	LNCaP	prostate:	n/a
16	chr11:8816428-8816478	U87	brain:	n/a
17	chr11:8808320-8808370	LNCaP	prostate:	n/a
18	chr11:8808320-8808370	ProgFib	skin:	n/a
19	chr11:8800270-8800320	SK-N-MC	brain:	n/a
20	chr11:8816428-8816478	HIPEpiC	eye:	n/a
21	chr11:8816428-8816478	MCF-7	breast:	n/a
22	chr11:8800270-8800320	GM12892	blood:	n/a
23	chr11:8800270-8800320	NB4	blood:	n/a
24	chr11:8821924-8821974	HUVEC	blood vessel:	n/a
25	chr11:8808320-8808370	Jurkat	blood:	n/a
26	chr11:8821924-8821974	Caco-2	colon:	n/a
27	chr11:8816428-8816478	AG10803	skin:	n/a
28	chr11:8800270-8800320	GM19239	blood:	n/a
29	chr11:8808320-8808370	HPAEpiC	pulmonary alveolar:	n/a
30	chr11:8793878-8793928	AG10803	skin:	n/a
31	chr11:8821924-8821974	HL-60	blood:	n/a
32	chr11:8816428-8816478	AoSMC	blood vessel:	n/a
33	chr11:8821924-8821974	CMK	blood:	n/a
34	chr11:8816428-8816478	HEEpiC	esophagus:	n/a
35	chr11:8800270-8800320	AG04450	lung:	fetal
36	chr11:8808320-8808370	HCPEpiC	choroid plexus:	n/a
37	chr11:8808320-8808370	HMEC	breast:	n/a
38	chr11:8793878-8793928	Hepatocyte	liver:	n/a
39	chr11:8793878-8793928	GM06990	blood:	n/a
40	chr11:8821924-8821974	AG04450	lung:	fetal
41	chr11:8821924-8821974	HCT-116	colon:	n/a
42	chr11:8800270-8800320	HCM	heart:	n/a
43	chr11:8800270-8800320	LNCaP	prostate:	n/a
44	chr11:8821924-8821974	PrEC	prostate:	n/a
45	chr11:8808320-8808370	SK-N-MC	brain:	n/a
46	chr11:8808320-8808370	HAEpiC	amniotic membrane:	n/a
47	chr11:8800270-8800320	A549	lung:	n/a
48	chr11:8816428-8816478	GM12892	blood:	n/a
49	chr11:8800270-8800320	Jurkat	blood:	n/a
50	chr11:8821924-8821974	Hepatocyte	liver:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:8806228..8807988-chr11:8810413..8812334,2	K562	blood:
2	chr11:8820429..8822256-chr11:8823665..8826630,2	K562	blood:
3	chr11:8811870..8814213-chr11:8819561..8821244,2	K562	blood:
4	chr11:8789292..8792139-chr11:8801689..8804373,2	K562	blood:
5	chr11:8714620..8716803-chr11:8793970..8795486,2	K562	blood:
6	chr11:8801841..8803945-chr11:8806888..8809278,2	MCF-7	breast:
7	chr11:8715578..8718169-chr11:8819916..8823970,3	MCF-7	breast:
8	chr11:8719301..8720930-chr11:8796904..8798885,2	K562	blood:
9	chr11:8792754..8796675-chr11:8797137..8799307,3	K562	blood:
10	chr11:8792754..8796675-chr11:8797137..8799307,3	K562	blood:
11	chr11:8823897..8825497-chr11:8829391..8832297,2	K562	blood:
12	chr11:8811870..8814213-chr11:8819561..8821244,2	K562	blood:
13	chr11:8825764..8827558-chr11:8831066..8834335,3	K562	blood:
14	chr11:8713389..8715952-chr11:8790656..8792768,2	K562	blood:
15	chr11:8706214..8708044-chr11:8804494..8806612,2	MCF-7	breast:
16	chr11:8709428..8711935-chr11:8797742..8799466,2	K562	blood:
17	chr11:8709572..8711665-chr11:8791796..8793909,2	MCF-7	breast:
18	chr11:8709766..8713200-chr11:8820077..8823864,3	K562	blood:
19	chr11:8799185..8801776-chr11:8804867..8806861,2	K562	blood:
20	chr11:8715976..8718057-chr11:8817200..8820115,2	K562	blood:
21	chr11:8820429..8822256-chr11:8823665..8826630,2	K562	blood:
22	chr11:8708821..8711720-chr11:8797773..8800794,3	MCF-7	breast:
23	chr11:8708277..8712745-chr11:8814108..8817920,5	MCF-7	breast:
24	chr11:8776493..8778441-chr11:8825146..8827348,2	MCF-7	breast:
25	chr11:8708263..8710064-chr11:8790794..8793308,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RPL27A-2	chr11:8806948-8807009	ENSG00000255159.1
2	lnc-RPL27A-2	chr11:8806088-8806104	ENSG00000255159.1
3	lnc-RPL27A-2	chr11:8808601-8808833	ENSG00000255159.1
4	lnc-RPL27A-2	chr11:8806703-8807009	ENSG00000255159.1
5	lnc-RPL27A-2	chr11:8805566-8805755	ENSG00000255159.1
6	lnc-RPL27A-2	chr11:8806703-8807318	ENSG00000255159.1

No data

Variant related genes	Relation type
ENSG00000255159	TF binding region
ST5	TF binding region
ENSG00000255159	CpG island
ST5	CpG island
ENSG00000255159	chromatin interactions
ENSG00000166441	chromatin interactions
ENSG00000254665	chromatin interactions
ENSG00000166444	chromatin interactions
ENSG00000212607	chromatin interactions

Extended variants
information (count: 1276 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:1276 , 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	rs4929936	chr11:8792622-8792623	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs145966017	chr11:8792632-8792633	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs185952692	chr11:8792650-8792651	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs559379480	chr11:8792659-8792660	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs551587965	chr11:8792663-8792664	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs138550659	chr11:8792678-8792679	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs141483223	chr11:8792722-8792723	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs146156225	chr11:8792728-8792729	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs566935321	chr11:8792729-8792730	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs536500200	chr11:8792741-8792742	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs190870970	chr11:8792743-8792744	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs528143652	chr11:8792758-8792759	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs570051356	chr11:8792770-8792771	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs538838800	chr11:8792773-8792774	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs139950992	chr11:8792803-8792804	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs572419766	chr11:8792860-8792861	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs541529501	chr11:8792897-8792898	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs554957218	chr11:8792912-8792913	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs574883751	chr11:8792916-8792917	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs543877935	chr11:8792925-8792926	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs562756458	chr11:8792931-8792932	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs146509652	chr11:8792939-8792940	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs548219876	chr11:8792950-8792951	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs531663469	chr11:8792954-8792955	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs546927100	chr11:8792955-8792956	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs183078080	chr11:8792957-8792958	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs149831685	chr11:8793017-8793018	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs568016563	chr11:8793035-8793036	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs527357927	chr11:8793044-8793045	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs200291928	chr11:8793052-8793053	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs146103596	chr11:8793077-8793078	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs186383060	chr11:8793107-8793108	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs66471685	chr11:8793109-8793110	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs146752028	chr11:8793113-8793114	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs567067769	chr11:8793151-8793152	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs75956011	chr11:8793155-8793156	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs550890519	chr11:8793176-8793177	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs529629204	chr11:8793211-8793212	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs570594256	chr11:8793239-8793240	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs190278995	chr11:8793249-8793250	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs570230709	chr11:8793264-8793265	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs558811149	chr11:8793372-8793373	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs36035137	chr11:8793474-8793475	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs182885013	chr11:8793495-8793496	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs144802678	chr11:8793505-8793506	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs117217791	chr11:8793538-8793539	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs59504764	chr11:8793543-8793544	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs575022035	chr11:8793554-8793555	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs187479497	chr11:8793557-8793558	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs554547959	chr11:8793561-8793562	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Breast cancer	19432969	CNVD
Alzheimer''s disease	17576883	CNVD
Long-qt syndrome	17576883	CNVD
Emphysema	19352772	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chordoma	18071362	CNVD
Breast cancer	16608533	CNVD
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
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
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Neuroblastoma	21124317	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Schizophrenia	21399695	CNVD
Gastric cancer	16891809	CNVD
Cancer	17160897	CNVD
Multiple myeloma	16616336	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Dysmorphic features	22052655	CNVD
Intellectual disability	22052655	CNVD
Obesity	22052655	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21785460	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Barrett''s syndrome	19417022	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:1274 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:8777400-8795800	Enhancers	Rectal Smooth Muscle	rectum
2	chr11:8779600-8799600	Weak transcription	Fetal Brain Male	brain
3	chr11:8781400-8794600	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr11:8784000-8794200	Weak transcription	Colonic Mucosa	Colon
5	chr11:8785200-8799400	Enhancers	Fetal Heart	heart
6	chr11:8786400-8794200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr11:8786600-8795400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr11:8786600-8795400	Enhancers	Stomach Mucosa	stomach
9	chr11:8786600-8798000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr11:8786600-8803000	Enhancers	Ovary	ovary
11	chr11:8787000-8797800	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr11:8787600-8795000	Weak transcription	Fetal Intestine Large	intestine
13	chr11:8788200-8794200	Weak transcription	Gastric	stomach
14	chr11:8788200-8797000	Weak transcription	Brain Hippocampus Middle	brain
15	chr11:8788600-8799600	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr11:8788800-8792800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
17	chr11:8788800-8794200	Weak transcription	H1 Cell Line	embryonic stem cell
18	chr11:8788800-8794200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr11:8788800-8794200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
20	chr11:8788800-8801400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr11:8788800-8808400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr11:8789000-8795400	Enhancers	HMEC	breast
23	chr11:8789000-8801200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr11:8789400-8794800	Weak transcription	Brain Anterior Caudate	brain
25	chr11:8789400-8797000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr11:8789400-8797400	Weak transcription	Brain Substantia Nigra	brain
27	chr11:8789400-8807600	Weak transcription	Fetal Kidney	kidney
28	chr11:8789600-8799400	Weak transcription	Brain Cingulate Gyrus	brain
29	chr11:8789600-8805800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr11:8790200-8793400	Weak transcription	Fetal Intestine Small	intestine
31	chr11:8790400-8793800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr11:8790400-8794000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr11:8790400-8794200	Weak transcription	Rectal Mucosa Donor 31	rectum
34	chr11:8790400-8795600	Weak transcription	Pancreatic Islets	Pancreatic Islet
35	chr11:8790400-8795800	Weak transcription	Small Intestine	intestine
36	chr11:8790600-8794400	Weak transcription	HUES6 Cell Line	embryonic stem cell
37	chr11:8790600-8796000	Weak transcription	Sigmoid Colon	Sigmoid Colon
38	chr11:8790800-8792800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr11:8790800-8792800	Weak transcription	HUVEC	blood vessel
40	chr11:8790800-8793800	Weak transcription	Placenta	Placenta
41	chr11:8790800-8794000	Weak transcription	Spleen	Spleen
42	chr11:8790800-8794200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr11:8790800-8794200	Weak transcription	Lung	lung
44	chr11:8790800-8795000	Weak transcription	Duodenum Mucosa	Duodenum
45	chr11:8790800-8797000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr11:8791000-8794400	Weak transcription	Fetal Lung	lung
47	chr11:8791200-8793600	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr11:8791200-8794200	Weak transcription	Placenta Amnion	Placenta Amnion
49	chr11:8791400-8792800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr11:8791400-8793200	Weak transcription	HSMMtube	muscle

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