Variant report

Variant	nsv428258
Chromosome Location	chr11:58700092-58878839
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2343)
CpG islands
(count:3054)
Chromatin interactive
region (count:26)
LncRNA
region (count:29)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2343 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:58874268-58874746	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:58792609-58792905	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:58713222-58713481	HepG2	liver:	n/a	n/a
4	ATF1	chr11:58779639-58779652	K562	blood:	n/a	n/a
5	ATF1	chr11:58864804-58864948	K562	blood:	n/a	n/a
6	ATF2	chr11:58869606-58870352	GM12878	blood:	n/a	n/a
7	ATF2	chr11:58864502-58864964	GM12878	blood:	n/a	n/a
8	ATF2	chr11:58869726-58870352	GM12878	blood:	n/a	n/a
9	ATF2	chr11:58831671-58832143	GM12878	blood:	n/a	n/a
10	ATF2	chr11:58825833-58826405	GM12878	blood:	n/a	n/a
11	ATF2	chr11:58874367-58874899	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr11:58874015-58875031	GM12878	blood:	n/a	n/a
13	ATF2	chr11:58831402-58832419	GM12878	blood:	n/a	n/a
14	ATF2	chr11:58874286-58874870	GM12878	blood:	n/a	n/a
15	ATF2	chr11:58874344-58874770	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF3	chr11:58869743-58869963	K562	blood:	n/a	n/a
17	BACH1	chr11:58825972-58826213	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr11:58869800-58870060	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr11:58873974-58874757	H1-hESC	embryonic stem cell:	n/a	chr11:58874543-58874557
20	BATF	chr11:58869559-58870293	GM12878	blood:	n/a	n/a
21	BATF	chr11:58831471-58831776	GM12878	blood:	n/a	n/a
22	BATF	chr11:58831416-58832275	GM12878	blood:	n/a	chr11:58831926-58831934
23	BATF	chr11:58826199-58826498	GM12878	blood:	n/a	n/a
24	BATF	chr11:58862752-58863071	GM12878	blood:	n/a	n/a
25	BATF	chr11:58875555-58875818	GM12878	blood:	n/a	chr11:58875662-58875670
26	BATF	chr11:58874419-58874727	GM12878	blood:	n/a	chr11:58874543-58874553 chr11:58874547-58874557 chr11:58874542-58874553
27	BATF	chr11:58875256-58875548	GM12878	blood:	n/a	n/a
28	BATF	chr11:58831786-58832150	GM12878	blood:	n/a	chr11:58831926-58831934
29	BATF	chr11:58818940-58819193	GM12878	blood:	n/a	n/a
30	BATF	chr11:58760001-58760259	GM12878	blood:	n/a	chr11:58760105-58760116
31	BCL11A	chr11:58831483-58831904	GM12878	blood:	n/a	n/a
32	BCL11A	chr11:58862711-58863079	GM12878	blood:	n/a	chr11:58862903-58862912
33	BCL11A	chr11:58869760-58870216	GM12878	blood:	n/a	n/a
34	BCL11A	chr11:58875271-58875606	GM12878	blood:	n/a	n/a
35	BCL11A	chr11:58862690-58863069	GM12878	blood:	n/a	chr11:58862903-58862912
36	BCL11A	chr11:58831528-58832157	GM12878	blood:	n/a	n/a
37	BCL11A	chr11:58818878-58819275	GM12878	blood:	n/a	chr11:58819091-58819100
38	BCL11A	chr11:58818899-58819262	GM12878	blood:	n/a	chr11:58819091-58819100
39	BCL11A	chr11:58869844-58870260	GM12878	blood:	n/a	n/a
40	BCL3	chr11:58869751-58870129	GM12878	blood:	n/a	n/a
41	BCL3	chr11:58831794-58832281	GM12878	blood:	n/a	n/a
42	BCLAF1	chr11:58873883-58874436	GM12878	blood:	n/a	chr11:58874084-58874097
43	BCLAF1	chr11:58869623-58870275	GM12878	blood:	n/a	n/a
44	BCLAF1	chr11:58869650-58870315	GM12878	blood:	n/a	n/a
45	BHLHE40	chr11:58792570-58792935	HepG2	liver:	n/a	chr11:58792752-58792765 chr11:58792748-58792769
46	BHLHE40	chr11:58820953-58821000	K562	blood:	n/a	n/a
47	BHLHE40	chr11:58874616-58874646	K562	blood:	n/a	n/a
48	BHLHE40	chr11:58874184-58874825	HepG2	liver:	n/a	n/a
49	BHLHE40	chr11:58869799-58869950	K562	blood:	n/a	n/a
50	BHLHE40	chr11:58865311-58865484	GM12878	blood:	n/a	n/a

(count:3054 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:58711078-58711128	H1-hESC	embryonic stem cell:	embryo
2	chr11:58873955-58874005	AoSMC	blood vessel:	n/a
3	chr11:58874635-58874685	PANC-1	pancreas:	n/a
4	chr11:58869823-58869873	NHBE	bronchial:	n/a
5	chr11:58711078-58711128	H1-hESC	embryonic stem cell:	embryo
6	chr11:58873955-58874005	AoSMC	blood vessel:	n/a
7	chr11:58874635-58874685	PANC-1	pancreas:	n/a
8	chr11:58869823-58869873	NHBE	bronchial:	n/a
9	chr11:58877370-58877420	HAEpiC	amniotic membrane:	n/a
10	chr11:58810187-58810237	HMEC	breast:	n/a
11	chr11:58874637-58874687	GM12878	blood:	n/a
12	chr11:58735304-58735354	HCT-116	colon:	n/a
13	chr11:58874348-58874398	T-47D	breast:	n/a
14	chr11:58874635-58874685	HNPCEpiC	eye:	n/a
15	chr11:58711078-58711128	HRCEpiC	kidney:	n/a
16	chr11:58830355-58830405	HRCEpiC	kidney:	n/a
17	chr11:58810187-58810237	NT2-D1	testis:	n/a
18	chr11:58826073-58826123	PFSK-1	brain:	n/a
19	chr11:58731433-58731483	NB4	blood:	n/a
20	chr11:58724252-58724302	CMK	blood:	n/a
21	chr11:58731505-58731555	GM12892	blood:	n/a
22	chr11:58826073-58826123	Hela-S3	cervix:	n/a
23	chr11:58825870-58825920	GM19239	blood:	n/a
24	chr11:58731634-58731684	BE2_C	brain:	n/a
25	chr11:58825714-58825764	HCM	heart:	n/a
26	chr11:58826414-58826464	MCF-7	breast:	n/a
27	chr11:58825870-58825920	PANC-1	pancreas:	n/a
28	chr11:58731104-58731154	GM12892	blood:	n/a
29	chr11:58869663-58869713	HEEpiC	esophagus:	n/a
30	chr11:58874637-58874687	A549	lung:	n/a
31	chr11:58828174-58828224	HIPEpiC	eye:	n/a
32	chr11:58874207-58874257	H1-hESC	embryonic stem cell:	embryo
33	chr11:58825714-58825764	GM12891	blood:	n/a
34	chr11:58731104-58731154	RPTEC	kidney:	n/a
35	chr11:58806952-58807002	Caco-2	colon:	n/a
36	chr11:58874645-58874695	SKMC	muscle:	n/a
37	chr11:58731634-58731684	PANC-1	pancreas:	n/a
38	chr11:58874635-58874685	AG09319	gingival:	n/a
39	chr11:58806952-58807002	SK-N-SH_RA	brain:	n/a
40	chr11:58830857-58830907	HCPEpiC	choroid plexus:	n/a
41	chr11:58731104-58731154	H1-hESC	embryonic stem cell:	embryo
42	chr11:58730897-58730947	Hela-S3	cervix:	n/a
43	chr11:58874645-58874695	H1-hESC	embryonic stem cell:	embryo
44	chr11:58826414-58826464	HEK293	kidney:	embryo
45	chr11:58731104-58731154	U87	brain:	n/a
46	chr11:58825714-58825764	Hepatocyte	liver:	n/a
47	chr11:58874637-58874687	ECC-1	luminal epithelium:	n/a
48	chr11:58830857-58830907	RPTEC	kidney:	n/a
49	chr11:58869979-58870029	K562	blood:	n/a
50	chr11:58731505-58731555	HRPEpiC	eye:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:58873861..58874546-chr5:111496427..111496981,2	Hela-S3	cervix:
2	chr11:58874735..58876453-chr11:58878007..58880480,2	MCF-7	breast:
3	chr11:58869989..58871867-chr11:58872289..58874332,2	MCF-7	breast:
4	chr11:58872425..58874544-chr11:58888169..58890358,2	MCF-7	breast:
5	chr11:58762969..58764487-chr11:58768997..58771127,2	K562	blood:
6	chr11:58873805..58875305-chr17:41466179..41467880,2	MCF-7	breast:
7	chr11:58762969..58764487-chr11:58768997..58771127,2	K562	blood:
8	chr11:58873708..58874686-chr11:63448916..63449711,2	Hela-S3	cervix:
9	chr11:58399679..58402149-chr11:58838160..58840024,2	K562	blood:
10	chr11:58721468..58724070-chr11:58726713..58729457,3	K562	blood:
11	chr11:58875510..58878300-chr11:58880309..58883300,3	MCF-7	breast:
12	chr11:58721468..58724070-chr11:58726713..58729457,3	K562	blood:
13	chr11:58869192..58871421-chr11:58911598..58913836,2	MCF-7	breast:
14	chr11:58873805..58876804-chr17:41466274..41467888,2	K562	blood:
15	chr11:58869989..58871867-chr11:58872289..58874332,2	MCF-7	breast:
16	chr11:58726086..58726653-chr11:58902781..58903961,3	K562	blood:
17	chr11:58830364..58831268-chr11:58873992..58874927,2	HCT-116	colon:
18	chr11:58729566..58731391-chr11:58732930..58735906,2	K562	blood:
19	chr11:58864668..58865554-chr11:58903471..58904061,2	MCF-7	breast:
20	chr11:58875233..58875940-chr12:49657802..49658323,2	Hela-S3	cervix:
21	chr11:58869769..58871706-chr11:58872515..58874019,2	MCF-7	breast:
22	chr11:58869769..58871706-chr11:58872515..58874019,2	MCF-7	breast:
23	chr11:58874735..58876453-chr11:58878007..58880480,2	MCF-7	breast:
24	chr11:58869975..58872858-chr11:58877240..58880132,2	MCF-7	breast:
25	chr11:58869975..58872858-chr11:58877240..58880132,2	MCF-7	breast:
26	chr11:58863409..58866220-chr11:58910202..58912249,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GLYATL2-2	chr11:58761476-58761524	NR_033853
2	lnc-GLYATL2-2	chr11:58820930-58821099	ENSG00000255240.1
3	lnc-GLYATL2-2	chr11:58825845-58825925	NR_033853
4	lnc-GLYATL2-2	chr11:58746601-58746798	NR_033853
5	lnc-GLYATL2-2	chr11:58746601-58746798	ENSG00000255240.1
6	lnc-GLYATL2-2	chr11:58736426-58736546	ENSG00000255240.1
7	lnc-GLYATL2-2	chr11:58825845-58825923	ENSG00000255240.1
8	lnc-GLYATL2-2	chr11:58725690-58726293	ENSG00000255240.1
9	lnc-GLYATL2-2	chr11:58818733-58818781	ENSG00000255240.1
10	lnc-GLYATL1-2	chr11:58710760-58710795	NONHSAT021491
11	lnc-FAM111A-1	chr11:58874709-58874769	NONHSAT021500
12	lnc-GLYATL1-2	chr11:58710789-58711139	NONHSAT021492
13	lnc-GLYATL2-2	chr11:58761476-58761524	ENSG00000255240.1
14	lnc-GLYATL2-4	chr11:58735069-58735764	NONHSAT021495
15	lnc-GLYATL2-2	chr11:58746601-58746758	ENSG00000255240.1
16	lnc-FAM111A-1	chr11:58877013-58877480	NONHSAT021500
17	lnc-GLYATL2-2	chr11:58736415-58736546	ENSG00000255240.1
18	lnc-GLYATL2-2	chr11:58701116-58703171	NR_033853
19	lnc-GLYATL2-2	chr11:58820930-58821099	NR_033853
20	lnc-FAM111A-1	chr11:58876141-58876185	NONHSAT021500
21	lnc-GLYATL1-2	chr11:58714519-58714734	NONHSAT021492
22	lnc-GLYATL1-2	chr11:58711016-58711139	NONHSAT021491
23	lnc-GLYATL2-2	chr11:58820930-58821099	ENSG00000255240.1
24	lnc-GLYATL2-2	chr11:58822768-58822919	ENSG00000255240.1
25	lnc-GLYATL2-2	chr11:58701116-58703171	ENSG00000255240.1
26	lnc-GLYATL1-2	chr11:58714519-58714948	NONHSAT021491
27	lnc-GLYATL2-2	chr11:58818733-58818781	NR_033853
28	lnc-GLYATL2-2	chr11:58818733-58818781	ENSG00000255240.1
29	lnc-GLYATL2-2	chr11:58825845-58826132	ENSG00000255240.1

No data

Variant related genes	Relation type
GLYATL1P1	TF binding region
ENSG00000255240	TF binding region
GLYATL1P3	TF binding region
GLYATL1P4	TF binding region
ENSG00000254877	TF binding region
ENSG00000254786	TF binding region
FAM111B	TF binding region
ENSG00000255523	TF binding region
GLYATL1	TF binding region
GLYATL1P1	CpG island
ENSG00000255240	CpG island
GLYATL1P3	CpG island
GLYATL1P4	CpG island
ENSG00000254877	CpG island
ENSG00000254786	CpG island
FAM111B	CpG island
ENSG00000255523	CpG island
GLYATL1	CpG island
ENSG00000245571	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000166801	chromatin interactions
ENSG00000133318	chromatin interactions
ENSG00000189057	chromatin interactions
ENSG00000224032	chromatin interactions
ENSG00000254877	chromatin interactions
CNOT6	miRNA target sites
GSPT1	miRNA target sites
KIF2A	miRNA target sites

Extended variants
information (count: 7115 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:7115 , 50 per page) page: 1 2 3 4 5 6 7 ... 143

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs376277521	chr11:58700184-58700185	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs531062543	chr11:58700214-58700215	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs573413273	chr11:58700303-58700304	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs552072895	chr11:58700356-58700357	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs570593639	chr11:58700361-58700362	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs534540286	chr11:58700412-58700413	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs546872494	chr11:58700455-58700456	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs568375595	chr11:58700460-58700461	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs535437870	chr11:58700484-58700485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs148256157	chr11:58700489-58700490	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs575392321	chr11:58700502-58700503	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs370785518	chr11:58700542-58700543	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs187159416	chr11:58700551-58700552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs201484641	chr11:58700588-58700589	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs12222597	chr11:58700597-58700598	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs541274549	chr11:58700604-58700605	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs75220513	chr11:58700643-58700644	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs574841556	chr11:58700726-58700727	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs541800069	chr11:58700727-58700728	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs563377602	chr11:58700774-58700775	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs142020980	chr11:58700779-58700780	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs546230321	chr11:58700828-58700829	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs481247	chr11:58700868-58700869	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs528252760	chr11:58700910-58700911	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs192017636	chr11:58700918-58700919	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs145717465	chr11:58700938-58700939	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs182974916	chr11:58700973-58700974	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs529247687	chr11:58700991-58700992	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs574939135	chr11:58701001-58701002	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs568789640	chr11:58701002-58701003	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs115399628	chr11:58701009-58701010	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs576956027	chr11:58701010-58701011	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs480196	chr11:58701011-58701012	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs187633672	chr11:58701030-58701031	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs75853723	chr11:58701055-58701056	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs114526297	chr11:58701072-58701073	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs542076033	chr11:58701099-58701100	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs73483072	chr11:58701105-58701106	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs528199835	chr11:58701112-58701113	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs538055030	chr11:58701181-58701182	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
41	rs117879143	chr11:58701219-58701220	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
42	rs564586795	chr11:58701220-58701221	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
43	rs528627474	chr11:58701270-58701271	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
44	rs544954056	chr11:58701271-58701272	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
45	rs376037177	chr11:58701286-58701287	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
46	rs540422158	chr11:58701287-58701288	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
47	rs193267874	chr11:58701305-58701306	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
48	rs376749136	chr11:58701323-58701324	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
49	rs550868000	chr11:58701330-58701331	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
50	rs569073265	chr11:58701414-58701415	Weak transcription Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Esophageal cancer	21851588	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16272173	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Pituitary adenoma	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Autism	22495309	CNVD
Autism	20808228	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	20164919	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1798 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:58696200-58700800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr11:58696200-58701400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr11:58696200-58701600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr11:58696200-58703800	Weak transcription	Thymus	Thymus
5	chr11:58699000-58700800	Weak transcription	Fetal Intestine Small	intestine
6	chr11:58699400-58700600	Weak transcription	Fetal Intestine Large	intestine
7	chr11:58699800-58704000	Enhancers	Liver	Liver
8	chr11:58700600-58701800	Enhancers	Fetal Intestine Large	intestine
9	chr11:58700800-58701800	Enhancers	Breast Myoepithelial Primary Cells	Breast
10	chr11:58700800-58701800	Enhancers	Fetal Intestine Small	intestine
11	chr11:58701200-58701600	Enhancers	Gastric	stomach
12	chr11:58701400-58702200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr11:58701600-58703800	Weak transcription	Gastric	stomach
14	chr11:58701800-58702200	Weak transcription	Fetal Intestine Large	intestine
15	chr11:58701800-58702200	Weak transcription	Fetal Intestine Small	intestine
16	chr11:58702200-58702600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr11:58702200-58703000	Enhancers	Fetal Intestine Large	intestine
18	chr11:58702200-58703000	Enhancers	Fetal Intestine Small	intestine
19	chr11:58702800-58703000	Weak transcription	Fetal Thymus	thymus
20	chr11:58703000-58705000	Enhancers	Fetal Thymus	thymus
21	chr11:58703000-58709200	Weak transcription	Fetal Intestine Large	intestine
22	chr11:58703000-58712800	Weak transcription	Fetal Intestine Small	intestine
23	chr11:58703800-58704000	Enhancers	Gastric	stomach
24	chr11:58703800-58704800	Enhancers	Thymus	Thymus
25	chr11:58704000-58705800	Weak transcription	Liver	Liver
26	chr11:58705800-58706800	Enhancers	Liver	Liver
27	chr11:58706800-58707000	Flanking Active TSS	Liver	Liver
28	chr11:58707000-58709000	Active TSS	Liver	Liver
29	chr11:58707200-58708400	Enhancers	HepG2	liver
30	chr11:58708400-58712600	Weak transcription	HepG2	liver
31	chr11:58709000-58710600	Flanking Active TSS	Liver	Liver
32	chr11:58709200-58709800	Enhancers	Fetal Intestine Large	intestine
33	chr11:58709400-58709600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr11:58709800-58712800	Weak transcription	Fetal Intestine Large	intestine
35	chr11:58710600-58710800	Enhancers	Liver	Liver
36	chr11:58710800-58712000	Enhancers	Breast Myoepithelial Primary Cells	Breast
37	chr11:58710800-58712600	Genic enhancers	Liver	Liver
38	chr11:58711000-58713400	Active TSS	Fetal Kidney	kidney
39	chr11:58712000-58712400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
40	chr11:58712400-58715400	Enhancers	Breast Myoepithelial Primary Cells	Breast
41	chr11:58712600-58713200	Flanking Active TSS	Liver	Liver
42	chr11:58712600-58713400	Enhancers	HepG2	liver
43	chr11:58712800-58713200	Enhancers	Fetal Intestine Large	intestine
44	chr11:58712800-58713400	Enhancers	Fetal Intestine Small	intestine
45	chr11:58712800-58714000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr11:58713200-58714400	Enhancers	Liver	Liver
47	chr11:58713400-58721800	Weak transcription	Fetal Intestine Small	intestine
48	chr11:58714400-58718000	Genic enhancers	Liver	Liver
49	chr11:58715600-58718600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
50	chr11:58718000-58720200	Weak transcription	Liver	Liver

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