Variant report

Variant	nsv554203
Chromosome Location	chr11:46399538-46406497
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:963)
CpG islands
(count:1099)
Chromatin interactive
region (count:29)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:963 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:46402101-46402260	K562	blood:	n/a	n/a
2	ATF2	chr11:46400834-46401165	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr11:46402173-46402624	GM12878	blood:	n/a	n/a
4	ATF2	chr11:46403673-46404035	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr11:46401888-46402790	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr11:46402216-46402605	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr11:46401888-46402246	K562	blood:	n/a	n/a
8	ATF3	chr11:46404810-46405028	K562	blood:	n/a	n/a
9	BACH1	chr11:46401422-46401426	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr11:46402342-46402912	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCL3	chr11:46402129-46402691	A549	lung:	n/a	chr11:46402337-46402346 chr11:46402354-46402363
12	BCL3	chr11:46402126-46402816	GM12878	blood:	n/a	chr11:46402337-46402346 chr11:46402354-46402363
13	BCLAF1	chr11:46402216-46402717	GM12878	blood:	n/a	chr11:46402337-46402346 chr11:46402354-46402363
14	BHLHE40	chr11:46403455-46403934	K562	blood:	n/a	n/a
15	BHLHE40	chr11:46402017-46402399	K562	blood:	n/a	n/a
16	BHLHE40	chr11:46404853-46404854	K562	blood:	n/a	n/a
17	CBX3	chr11:46399359-46399798	K562	blood:	n/a	n/a
18	CBX3	chr11:46399430-46399768	K562	blood:	n/a	n/a
19	CBX3	chr11:46401135-46401556	K562	blood:	n/a	n/a
20	CBX3	chr11:46401890-46402414	K562	blood:	n/a	n/a
21	CBX3	chr11:46403354-46403695	K562	blood:	n/a	n/a
22	CCNT2	chr11:46401934-46404360	K562	blood:	n/a	chr11:46403154-46403163 chr11:46403192-46403201 chr11:46402348-46402357 chr11:46403148-46403157 chr11:46402409-46402418 chr11:46403179-46403188 chr11:46403705-46403714
23	CCNT2	chr11:46400579-46401151	K562	blood:	n/a	chr11:46400838-46400847
24	CCNT2	chr11:46401360-46401478	K562	blood:	n/a	n/a
25	CEBPB	chr11:46400904-46400923	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr11:46402302-46402464	Hela-S3	cervix:	n/a	n/a
27	CEBPD	chr11:46402104-46402629	HepG2	liver:	n/a	n/a
28	CHD1	chr11:46401169-46401282	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD1	chr11:46402441-46402478	GM12878	blood:	n/a	n/a
30	CHD1	chr11:46402000-46402255	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr11:46402024-46402856	GM12878	blood:	n/a	n/a
32	CHD2	chr11:46401946-46402590	Hela-S3	cervix:	n/a	n/a
33	CHD2	chr11:46405012-46405073	K562	blood:	n/a	n/a
34	CHD2	chr11:46404239-46404383	K562	blood:	n/a	n/a
35	CHD2	chr11:46403604-46403862	K562	blood:	n/a	n/a
36	CHD2	chr11:46402310-46402783	HepG2	liver:	n/a	n/a
37	CHD2	chr11:46403442-46403586	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD2	chr11:46402090-46402904	K562	blood:	n/a	n/a
39	CHD2	chr11:46405934-46405954	K562	blood:	n/a	n/a
40	CHD2	chr11:46401974-46402899	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD2	chr11:46401145-46401343	K562	blood:	n/a	n/a
42	CREB1	chr11:46402183-46402437	A549	lung:	n/a	n/a
43	CREB1	chr11:46401916-46403009	HepG2	liver:	n/a	n/a
44	CREB1	chr11:46401925-46402542	GM12878	blood:	n/a	n/a
45	CREB1	chr11:46401903-46402573	K562	blood:	n/a	n/a
46	CTBP2	chr11:46401904-46402847	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTBP2	chr11:46403296-46404189	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr11:46404718-46405059	A549	lung:	n/a	chr11:46404902-46404911 chr11:46404902-46404915 chr11:46404901-46404922 chr11:46404899-46404917 chr11:46404900-46404916
49	CTCF	chr11:46404800-46404950	A549	lung:	n/a	chr11:46404902-46404911 chr11:46404902-46404915 chr11:46404901-46404922 chr11:46404899-46404917 chr11:46404900-46404916
50	CTCF	chr11:46404840-46404990	HMF	breast:	n/a	chr11:46404902-46404911 chr11:46404902-46404915 chr11:46404901-46404922 chr11:46404899-46404917 chr11:46404900-46404916

(count:1099 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:46402210-46402260	GM12892	blood:	n/a
2	chr11:46402210-46402260	GM12892	blood:	n/a
3	chr11:46402051-46402101	HCT-116	colon:	n/a
4	chr11:46402051-46402101	BE2_C	brain:	n/a
5	chr11:46400378-46400428	U87	brain:	n/a
6	chr11:46403923-46403973	MCF-7	breast:	n/a
7	chr11:46403416-46403466	Jurkat	blood:	n/a
8	chr11:46403617-46403667	U87	brain:	n/a
9	chr11:46403617-46403667	AG09309	skin:	n/a
10	chr11:46403409-46403459	U87	brain:	n/a
11	chr11:46402210-46402260	GM12891	blood:	n/a
12	chr11:46403617-46403667	IMR90	lung:	fetal
13	chr11:46403087-46403137	NHBE	bronchial:	n/a
14	chr11:46402601-46402651	HRPEpiC	eye:	n/a
15	chr11:46402506-46402556	T-47D	breast:	n/a
16	chr11:46402548-46402598	NHBE	bronchial:	n/a
17	chr11:46402949-46402999	HNPCEpiC	eye:	n/a
18	chr11:46403409-46403459	A549	lung:	n/a
19	chr11:46402051-46402101	PFSK-1	brain:	n/a
20	chr11:46403087-46403137	HCM	heart:	n/a
21	chr11:46403087-46403137	PANC-1	pancreas:	n/a
22	chr11:46403087-46403137	Caco-2	colon:	n/a
23	chr11:46402601-46402651	NHDF-neo	bronchial:	n/a
24	chr11:46402210-46402260	SK-N-SH_RA	brain:	n/a
25	chr11:46402535-46402585	HIPEpiC	eye:	n/a
26	chr11:46401447-46401497	ovcar-3	ovarian:	n/a
27	chr11:46400378-46400428	ProgFib	skin:	n/a
28	chr11:46402666-46402716	GM12892	blood:	n/a
29	chr11:46402548-46402598	HL-60	blood:	n/a
30	chr11:46403409-46403459	PrEC	prostate:	n/a
31	chr11:46402548-46402598	CMK	blood:	n/a
32	chr11:46403923-46403973	RPTEC	kidney:	n/a
33	chr11:46400378-46400428	SK-N-SH_RA	brain:	n/a
34	chr11:46403087-46403137	HAEpiC	amniotic membrane:	n/a
35	chr11:46403416-46403466	NT2-D1	testis:	n/a
36	chr11:46403409-46403459	GM19239	blood:	n/a
37	chr11:46402506-46402556	PFSK-1	brain:	n/a
38	chr11:46402601-46402651	HCM	heart:	n/a
39	chr11:46403409-46403459	ECC-1	luminal epithelium:	n/a
40	chr11:46403923-46403973	AG04450	lung:	fetal
41	chr11:46405046-46405096	HepG2	liver:	n/a
42	chr11:46402051-46402101	AG09309	skin:	n/a
43	chr11:46401447-46401497	AG04449	skin:	fetal
44	chr11:46402949-46402999	GM06990	blood:	n/a
45	chr11:46403923-46403973	ProgFib	skin:	n/a
46	chr11:46401702-46401752	AG04449	skin:	fetal
47	chr11:46402535-46402585	ovcar-3	ovarian:	n/a
48	chr11:46403416-46403466	GM06990	blood:	n/a
49	chr11:46402666-46402716	NT2-D1	testis:	n/a
50	chr11:46403416-46403466	PANC-1	pancreas:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:46401836..46403864-chr11:46637074..46639458,2	K562	blood:
2	chr11:46405206..46407245-chr11:46550618..46552285,2	K562	blood:
3	chr11:46404460..46405392-chr11:46550904..46551508,2	MCF-7	breast:
4	chr11:46387947..46390422-chr11:46401426..46404815,4	MCF-7	breast:
5	chr11:46399063..46400618-chr11:46400770..46402809,2	MCF-7	breast:
6	chr11:46368921..46370887-chr11:46401609..46403776,2	MCF-7	breast:
7	chr11:46391583..46394850-chr11:46399666..46402869,4	MCF-7	breast:
8	chr11:46389075..46389843-chr11:46400385..46401154,2	K562	blood:
9	chr11:46256874..46260563-chr11:46399060..46405748,9	K562	blood:
10	chr11:46404830..46405368-chr11:46550578..46551221,2	MCF-7	breast:
11	chr11:46383271..46387552-chr11:46403551..46406378,4	MCF-7	breast:
12	chr11:46141914..46143962-chr11:46401995..46404790,2	K562	blood:
13	chr11:46391433..46393341-chr11:46403120..46407243,3	MCF-7	breast:
14	chr11:46403212..46404191-chr8:23386218..23387002,2	HCT-116	colon:
15	chr11:46393877..46398500-chr11:46401419..46405642,6	MCF-7	breast:
16	chr11:46404862..46405373-chr11:46413237..46414117,2	MCF-7	breast:
17	chr11:46367411..46370383-chr11:46395468..46399934,4	K562	blood:
18	chr11:46316878..46318719-chr11:46403768..46406390,2	K562	blood:
19	chr11:46399063..46400618-chr11:46400770..46402809,2	MCF-7	breast:
20	chr11:46368689..46375486-chr11:46400770..46406098,12	K562	blood:
21	chr11:46402485..46405164-chr11:46638326..46640546,2	MCF-7	breast:
22	chr11:46382914..46384504-chr11:46401158..46403727,3	MCF-7	breast:
23	chr11:46401780..46403457-chr11:47290200..47292891,2	MCF-7	breast:
24	chr11:46404223..46405874-chr6:34202535..34205359,2	K562	blood:
25	chr11:46368337..46369929-chr11:46403347..46406253,2	MCF-7	breast:
26	chr11:46404448..46405323-chr11:46559050..46559932,2	K562	blood:
27	chr11:46401089..46404766-chr11:46549861..46553085,3	K562	blood:
28	chr11:46404499..46405688-chr11:46559322..46559979,3	MCF-7	breast:
29	chr11:46402912..46405362-chr11:46740261..46742073,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MDK-2	chr11:46399520-46399779	NONHSAT021173
2	lnc-MDK-2	chr11:46400007-46400477	NONHSAT021173

No data

Variant related genes	Relation type
MDK	TF binding region
MDK	CpG island
ENSG00000110492	chromatin interactions
ENSG00000137309	chromatin interactions
ENSG00000147454	chromatin interactions
ENSG00000254639	chromatin interactions
ENSG00000175224	chromatin interactions
ENSG00000180210	chromatin interactions
ENSG00000110514	chromatin interactions
ENSG00000264102	chromatin interactions
ENSG00000180423	chromatin interactions
ENSG00000110497	chromatin interactions
ENSG00000149091	chromatin interactions
ENSG00000135365	chromatin interactions

Extended variants
information (count: 267 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:267 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2279465	chr11:46399538-46399539	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs190388649	chr11:46399580-46399581	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
3	rs182583580	chr11:46399587-46399588	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
4	rs546627213	chr11:46399601-46399602	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
5	rs566732723	chr11:46399664-46399665	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
6	rs527684798	chr11:46399670-46399671	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
7	rs146368494	chr11:46399714-46399715	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
8	rs552561982	chr11:46399720-46399721	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
9	rs113907444	chr11:46399737-46399738	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
10	rs569445114	chr11:46399739-46399740	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
11	rs369155259	chr11:46399741-46399742	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
12	rs373262863	chr11:46399743-46399744	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
13	rs376728224	chr11:46399768-46399769	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
14	rs200913050	chr11:46399774-46399775	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
15	rs567402245	chr11:46399792-46399793	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs536331541	chr11:46399841-46399842	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs11038880	chr11:46399901-46399902	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs116227656	chr11:46399915-46399916	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs368629184	chr11:46399928-46399929	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs374018594	chr11:46399955-46399956	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs371536427	chr11:46399959-46399960	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs199549907	chr11:46399973-46399974	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs200489928	chr11:46399974-46399975	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs374438025	chr11:46399988-46399989	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs202186891	chr11:46399990-46399991	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs377041756	chr11:46399994-46399995	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs200519115	chr11:46400000-46400001	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs544040980	chr11:46400001-46400002	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs142463622	chr11:46400041-46400042	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
30	rs560736568	chr11:46400042-46400043	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
31	rs370171517	chr11:46400046-46400047	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
32	rs374796626	chr11:46400073-46400074	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
33	rs368086092	chr11:46400093-46400094	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
34	rs372048533	chr11:46400097-46400098	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
35	rs185310252	chr11:46400099-46400100	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
36	rs540304111	chr11:46400108-46400109	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
37	rs139662183	chr11:46400150-46400151	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
38	rs532364214	chr11:46400163-46400164	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
39	rs552839258	chr11:46400165-46400166	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
40	rs142015463	chr11:46400192-46400193	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
41	rs11827909	chr11:46400258-46400259	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs538861964	chr11:46400274-46400275	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
43	rs118085099	chr11:46400281-46400282	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
44	rs76614572	chr11:46400357-46400358	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
45	rs150701212	chr11:46400406-46400407	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
46	rs116789080	chr11:46400411-46400412	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
47	rs566463578	chr11:46400446-46400447	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
48	rs374051540	chr11:46400525-46400526	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs367894766	chr11:46400533-46400534	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs146351680	chr11:46400550-46400551	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Parathyroid adenoma	22454399	CNVD
Medulloblastoma	21979893	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
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	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
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Chordoma	18071362	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21364760	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Myelofibrosis	22110671	CNVD
Melanoma	18172304	CNVD
Intracranial ependymoma	16609018	CNVD
Myxofibrosarcoma	16751306	CNVD
Potocki-Shaffer syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	16608533	CNVD
Hirschsprung''s Disease	21712996	CNVD
Follicular lymphoma	20505157	CNVD
Colorectal cancer	21128281	CNVD
Breast cancer	20409316	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Mantle cell lymphoma	19029149	CNVD
Glioblastoma multiforme	21138945	CNVD
Prostate cancer	18632612	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Melanoma	17363583	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:913 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:46383600-46402000	Weak transcription	Fetal Brain Male	brain
2	chr11:46385200-46400600	Strong transcription	Thymus	Thymus
3	chr11:46385400-46401200	Strong transcription	Dnd41	blood
4	chr11:46386000-46402200	Weak transcription	NHDF-Ad	bronchial
5	chr11:46388600-46400200	Strong transcription	Gastric	stomach
6	chr11:46388800-46400600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
7	chr11:46389000-46399600	Strong transcription	Primary neutrophils fromperipheralblood	blood
8	chr11:46389000-46399600	Strong transcription	Monocytes-CD14+_RO01746	blood
9	chr11:46389000-46402000	Weak transcription	Right Atrium	heart
10	chr11:46389400-46400200	Strong transcription	iPS-15b Cell Line	embryonic stem cell
11	chr11:46389400-46400400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
12	chr11:46389400-46401400	Strong transcription	Primary T cells from cord blood	blood
13	chr11:46389600-46399800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr11:46389600-46400200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
15	chr11:46389600-46400200	Strong transcription	Liver	Liver
16	chr11:46389600-46400200	Strong transcription	Left Ventricle	heart
17	chr11:46389600-46400200	Strong transcription	Skeletal Muscle Female	skeletal muscle
18	chr11:46389600-46400400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
19	chr11:46389600-46400400	Strong transcription	Adipose Nuclei	Adipose
20	chr11:46389600-46400400	Strong transcription	Brain Inferior Temporal Lobe	brain
21	chr11:46389600-46401200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr11:46389600-46401800	Weak transcription	Stomach Mucosa	stomach
23	chr11:46389800-46400000	Strong transcription	Pancreas	Pancrea
24	chr11:46389800-46400200	Strong transcription	Primary T helper cells fromperipheralblood	blood
25	chr11:46389800-46400200	Strong transcription	Brain Cingulate Gyrus	brain
26	chr11:46389800-46400600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr11:46389800-46401000	Strong transcription	Fetal Thymus	thymus
28	chr11:46390000-46399600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
29	chr11:46390000-46400000	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
30	chr11:46390200-46400000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
31	chr11:46390200-46400400	Strong transcription	Primary T helper cells PMA-I stimulated	--
32	chr11:46390200-46401200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr11:46391000-46399800	Strong transcription	Skeletal Muscle Male	skeletal muscle
34	chr11:46391000-46402000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr11:46391200-46400400	Strong transcription	Fetal Brain Female	brain
36	chr11:46391400-46400400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr11:46391400-46400600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr11:46391400-46402200	Weak transcription	NH-A	brain
39	chr11:46391600-46399800	Strong transcription	Sigmoid Colon	Sigmoid Colon
40	chr11:46391600-46400200	Strong transcription	Brain Germinal Matrix	brain
41	chr11:46391600-46400200	Strong transcription	NHLF	lung
42	chr11:46391600-46400400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr11:46391600-46400600	Weak transcription	Hela-S3	cervix
44	chr11:46391600-46400800	Weak transcription	K562	blood
45	chr11:46391800-46399800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr11:46391800-46399800	Strong transcription	Stomach Smooth Muscle	stomach
47	chr11:46391800-46399800	Weak transcription	HepG2	liver
48	chr11:46391800-46400000	Strong transcription	Brain Hippocampus Middle	brain
49	chr11:46391800-46400200	Strong transcription	HUES6 Cell Line	embryonic stem cell
50	chr11:46391800-46400400	Strong transcription	Primary T cells fromperipheralblood	blood

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