Variant report

Variant	esv3393019
Chromosome Location	chr11:58679419-58880845
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2745)
CpG islands
(count:3301)
Chromatin interactive
region (count:30)
LncRNA
region (count:31)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2745 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:58792609-58792905	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:58713222-58713481	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:58693760-58694429	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:58874268-58874746	HepG2	liver:	n/a	n/a
5	ATF1	chr11:58691061-58691064	K562	blood:	n/a	n/a
6	ATF1	chr11:58779639-58779652	K562	blood:	n/a	n/a
7	ATF1	chr11:58864804-58864948	K562	blood:	n/a	n/a
8	ATF2	chr11:58831402-58832419	GM12878	blood:	n/a	n/a
9	ATF2	chr11:58825833-58826405	GM12878	blood:	n/a	n/a
10	ATF2	chr11:58874015-58875031	GM12878	blood:	n/a	n/a
11	ATF2	chr11:58831671-58832143	GM12878	blood:	n/a	n/a
12	ATF2	chr11:58874286-58874870	GM12878	blood:	n/a	n/a
13	ATF2	chr11:58874367-58874899	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr11:58874344-58874770	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr11:58864502-58864964	GM12878	blood:	n/a	n/a
16	ATF2	chr11:58869606-58870352	GM12878	blood:	n/a	n/a
17	ATF2	chr11:58694851-58695251	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr11:58869726-58870352	GM12878	blood:	n/a	n/a
19	ATF3	chr11:58869743-58869963	K562	blood:	n/a	n/a
20	BACH1	chr11:58690792-58691378	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr11:58873974-58874757	H1-hESC	embryonic stem cell:	n/a	chr11:58874543-58874557
22	BACH1	chr11:58825972-58826213	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr11:58869800-58870060	H1-hESC	embryonic stem cell:	n/a	n/a
24	BATF	chr11:58874419-58874727	GM12878	blood:	n/a	chr11:58874543-58874553 chr11:58874547-58874557 chr11:58874542-58874553
25	BATF	chr11:58831471-58831776	GM12878	blood:	n/a	n/a
26	BATF	chr11:58831416-58832275	GM12878	blood:	n/a	chr11:58831926-58831934
27	BATF	chr11:58818940-58819193	GM12878	blood:	n/a	n/a
28	BATF	chr11:58831786-58832150	GM12878	blood:	n/a	chr11:58831926-58831934
29	BATF	chr11:58875256-58875548	GM12878	blood:	n/a	n/a
30	BATF	chr11:58760001-58760259	GM12878	blood:	n/a	chr11:58760105-58760116
31	BATF	chr11:58862752-58863071	GM12878	blood:	n/a	n/a
32	BATF	chr11:58826199-58826498	GM12878	blood:	n/a	n/a
33	BATF	chr11:58869559-58870293	GM12878	blood:	n/a	n/a
34	BATF	chr11:58875555-58875818	GM12878	blood:	n/a	chr11:58875662-58875670
35	BCL11A	chr11:58831483-58831904	GM12878	blood:	n/a	n/a
36	BCL11A	chr11:58875271-58875606	GM12878	blood:	n/a	n/a
37	BCL11A	chr11:58862711-58863079	GM12878	blood:	n/a	chr11:58862903-58862912
38	BCL11A	chr11:58831528-58832157	GM12878	blood:	n/a	n/a
39	BCL11A	chr11:58818899-58819262	GM12878	blood:	n/a	chr11:58819091-58819100
40	BCL11A	chr11:58818878-58819275	GM12878	blood:	n/a	chr11:58819091-58819100
41	BCL11A	chr11:58869844-58870260	GM12878	blood:	n/a	n/a
42	BCL11A	chr11:58869760-58870216	GM12878	blood:	n/a	n/a
43	BCL11A	chr11:58862690-58863069	GM12878	blood:	n/a	chr11:58862903-58862912
44	BCL3	chr11:58831794-58832281	GM12878	blood:	n/a	n/a
45	BCL3	chr11:58869751-58870129	GM12878	blood:	n/a	n/a
46	BCLAF1	chr11:58869623-58870275	GM12878	blood:	n/a	n/a
47	BCLAF1	chr11:58869650-58870315	GM12878	blood:	n/a	n/a
48	BCLAF1	chr11:58873883-58874436	GM12878	blood:	n/a	chr11:58874084-58874097
49	BHLHE40	chr11:58869743-58870232	GM12878	blood:	n/a	n/a
50	BHLHE40	chr11:58874616-58874646	K562	blood:	n/a	n/a

(count:3301 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:58696069-58696119	Hepatocyte	liver:	n/a
2	chr11:58874608-58874658	T-47D	breast:	n/a
3	chr11:58873823-58873873	HUVEC	blood vessel:	n/a
4	chr11:58735304-58735354	PFSK-1	brain:	n/a
5	chr11:58870494-58870544	GM06990	blood:	n/a
6	chr11:58830857-58830907	IMR90	lung:	fetal
7	chr11:58825714-58825764	HRPEpiC	eye:	n/a
8	chr11:58696069-58696119	Hepatocyte	liver:	n/a
9	chr11:58874608-58874658	T-47D	breast:	n/a
10	chr11:58873823-58873873	HUVEC	blood vessel:	n/a
11	chr11:58735304-58735354	PFSK-1	brain:	n/a
12	chr11:58870494-58870544	GM06990	blood:	n/a
13	chr11:58830857-58830907	IMR90	lung:	fetal
14	chr11:58825714-58825764	HRPEpiC	eye:	n/a
15	chr11:58874635-58874685	ProgFib	skin:	n/a
16	chr11:58830355-58830405	PrEC	prostate:	n/a
17	chr11:58825714-58825764	HepG2	liver:	n/a
18	chr11:58870075-58870125	HCF	heart:	n/a
19	chr11:58736081-58736131	HAEpiC	amniotic membrane:	n/a
20	chr11:58869663-58869713	K562	blood:	n/a
21	chr11:58735304-58735354	IMR90	lung:	fetal
22	chr11:58869979-58870029	NH-A	brain:	n/a
23	chr11:58870494-58870544	HCF	heart:	n/a
24	chr11:58877370-58877420	ProgFib	skin:	n/a
25	chr11:58869663-58869713	GM12892	blood:	n/a
26	chr11:58731634-58731684	U87	brain:	n/a
27	chr11:58874608-58874658	SK-N-MC	brain:	n/a
28	chr11:58731505-58731555	HCT-116	colon:	n/a
29	chr11:58710158-58710208	GM12892	blood:	n/a
30	chr11:58694950-58695000	SKMC	muscle:	n/a
31	chr11:58710158-58710208	HPAEpiC	pulmonary alveolar:	n/a
32	chr11:58873955-58874005	PFSK-1	brain:	n/a
33	chr11:58695093-58695143	AG10803	skin:	n/a
34	chr11:58826073-58826123	HAEpiC	amniotic membrane:	n/a
35	chr11:58874645-58874695	PrEC	prostate:	n/a
36	chr11:58736104-58736154	SAEC	small airway:	n/a
37	chr11:58826073-58826123	AG09319	gingival:	n/a
38	chr11:58874733-58874783	Jurkat	blood:	n/a
39	chr11:58873823-58873873	ovcar-3	ovarian:	n/a
40	chr11:58724252-58724302	HCF	heart:	n/a
41	chr11:58869823-58869873	LNCaP	prostate:	n/a
42	chr11:58711078-58711128	NH-A	brain:	n/a
43	chr11:58736104-58736154	HIPEpiC	eye:	n/a
44	chr11:58869823-58869873	NHBE	bronchial:	n/a
45	chr11:58696069-58696119	PANC-1	pancreas:	n/a
46	chr11:58833356-58833406	GM12892	blood:	n/a
47	chr11:58826414-58826464	HNPCEpiC	eye:	n/a
48	chr11:58873823-58873873	BE2_C	brain:	n/a
49	chr11:58869979-58870029	ovcar-3	ovarian:	n/a
50	chr11:58874637-58874687	BJ	skin:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:58873708..58874686-chr11:63448916..63449711,2	Hela-S3	cervix:
2	chr11:58864668..58865554-chr11:58903471..58904061,2	MCF-7	breast:
3	chr11:58869769..58871706-chr11:58872515..58874019,2	MCF-7	breast:
4	chr11:58875233..58875940-chr12:49657802..49658323,2	Hela-S3	cervix:
5	chr11:58762969..58764487-chr11:58768997..58771127,2	K562	blood:
6	chr11:58869975..58872858-chr11:58877240..58880132,2	MCF-7	breast:
7	chr11:58721468..58724070-chr11:58726713..58729457,3	K562	blood:
8	chr11:58726086..58726653-chr11:58902781..58903961,3	K562	blood:
9	chr11:58875510..58878300-chr11:58880309..58883300,3	MCF-7	breast:
10	chr11:58678524..58679504-chr6:58776958..58777672,3	MCF-7	breast:
11	chr11:58869989..58871867-chr11:58872289..58874332,2	MCF-7	breast:
12	chr11:58874735..58876453-chr11:58878007..58880480,2	MCF-7	breast:
13	chr11:58762969..58764487-chr11:58768997..58771127,2	K562	blood:
14	chr11:58874735..58876453-chr11:58878007..58880480,2	MCF-7	breast:
15	chr11:58678524..58679504-chr6:58777166..58777745,2	MCF-7	breast:
16	chr11:58421165..58421796-chr11:58687413..58688096,2	MCF-7	breast:
17	chr11:58873805..58875305-chr17:41466179..41467880,2	MCF-7	breast:
18	chr11:58873861..58874546-chr5:111496427..111496981,2	Hela-S3	cervix:
19	chr11:58875510..58878300-chr11:58880309..58883300,3	MCF-7	breast:
20	chr11:58863409..58866220-chr11:58910202..58912249,2	K562	blood:
21	chr11:58873805..58876804-chr17:41466274..41467888,2	K562	blood:
22	chr11:58721468..58724070-chr11:58726713..58729457,3	K562	blood:
23	chr11:58869769..58871706-chr11:58872515..58874019,2	MCF-7	breast:
24	chr11:58869989..58871867-chr11:58872289..58874332,2	MCF-7	breast:
25	chr11:58872425..58874544-chr11:58888169..58890358,2	MCF-7	breast:
26	chr11:58830364..58831268-chr11:58873992..58874927,2	HCT-116	colon:
27	chr11:58399679..58402149-chr11:58838160..58840024,2	K562	blood:
28	chr11:58729566..58731391-chr11:58732930..58735906,2	K562	blood:
29	chr11:58869975..58872858-chr11:58877240..58880132,2	MCF-7	breast:
30	chr11:58869192..58871421-chr11:58911598..58913836,2	MCF-7	breast:

(count:31 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GLYATL2-2	chr11:58746601-58746798	NR_033853
2	lnc-GLYATL1-2	chr11:58714519-58714948	NONHSAT021491
3	lnc-GLYATL2-1	chr11:58684488-58684757	ENSG00000255523.1
4	lnc-GLYATL2-2	chr11:58736415-58736546	ENSG00000255240.1
5	lnc-FAM111A-1	chr11:58876141-58876185	NONHSAT021500
6	lnc-GLYATL2-2	chr11:58701116-58703171	NR_033853
7	lnc-FAM111A-1	chr11:58874709-58874769	NONHSAT021500
8	lnc-GLYATL2-2	chr11:58825845-58826132	ENSG00000255240.1
9	lnc-GLYATL2-2	chr11:58822768-58822919	ENSG00000255240.1
10	lnc-GLYATL2-2	chr11:58736426-58736546	ENSG00000255240.1
11	lnc-GLYATL1-2	chr11:58710789-58711139	NONHSAT021492
12	lnc-GLYATL2-2	chr11:58725690-58726293	ENSG00000255240.1
13	lnc-GLYATL2-1	chr11:58695790-58696162	ENSG00000255523.1
14	lnc-GLYATL2-2	chr11:58820930-58821099	ENSG00000255240.1
15	lnc-GLYATL2-2	chr11:58820930-58821099	ENSG00000255240.1
16	lnc-GLYATL2-2	chr11:58818733-58818781	ENSG00000255240.1
17	lnc-GLYATL1-2	chr11:58710760-58710795	NONHSAT021491
18	lnc-GLYATL2-2	chr11:58746601-58746758	ENSG00000255240.1
19	lnc-GLYATL2-2	chr11:58701116-58703171	ENSG00000255240.1
20	lnc-GLYATL2-2	chr11:58825845-58825923	ENSG00000255240.1
21	lnc-GLYATL2-2	chr11:58818733-58818781	NR_033853
22	lnc-GLYATL2-2	chr11:58820930-58821099	NR_033853
23	lnc-GLYATL2-4	chr11:58735069-58735764	NONHSAT021495
24	lnc-GLYATL2-2	chr11:58818733-58818781	ENSG00000255240.1
25	lnc-GLYATL1-2	chr11:58714519-58714734	NONHSAT021492
26	lnc-GLYATL2-2	chr11:58761476-58761524	NR_033853
27	lnc-GLYATL2-2	chr11:58746601-58746798	ENSG00000255240.1
28	lnc-FAM111A-1	chr11:58877013-58877480	NONHSAT021500
29	lnc-GLYATL2-2	chr11:58825845-58825925	NR_033853
30	lnc-GLYATL2-2	chr11:58761476-58761524	ENSG00000255240.1
31	lnc-GLYATL1-2	chr11:58711016-58711139	NONHSAT021491

No data

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

Extended variants
information (count: 7894 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:7894 , 50 per page) page: 1 2 3 4 5 6 7 ... 158

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs540196997	chr11:58679426-58679427	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs553691523	chr11:58679448-58679449	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs555445029	chr11:58679455-58679456	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs80168849	chr11:58679457-58679458	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs573779847	chr11:58679505-58679506	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs376257228	chr11:58679629-58679630	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs201166255	chr11:58679709-58679710	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs202004371	chr11:58679733-58679734	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs530978060	chr11:58679749-58679750	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs556092767	chr11:58679839-58679840	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs546400187	chr11:58679843-58679844	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs145218907	chr11:58679868-58679869	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs182700778	chr11:58679899-58679900	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs78099239	chr11:58679916-58679917	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs149215816	chr11:58679926-58679927	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs370410898	chr11:58679958-58679959	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs550760765	chr11:58680042-58680043	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs569354891	chr11:58680057-58680058	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs142472924	chr11:58680059-58680060	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs146838797	chr11:58680070-58680071	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs140673437	chr11:58680084-58680085	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs534133205	chr11:58680095-58680096	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs186019544	chr11:58680105-58680106	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs144637218	chr11:58680126-58680127	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs11229692	chr11:58680127-58680128	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs560484083	chr11:58680225-58680226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs544211777	chr11:58680227-58680228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs34147334	chr11:58680237-58680238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs540383	chr11:58680243-58680244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs79814934	chr11:58680289-58680290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs577672108	chr11:58680312-58680313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs12285888	chr11:58680407-58680408	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs138594468	chr11:58680449-58680450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs528737941	chr11:58680479-58680480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs540558763	chr11:58680493-58680494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs562057495	chr11:58680498-58680499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs529240677	chr11:58680524-58680525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs550954422	chr11:58680535-58680536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs569211867	chr11:58680564-58680565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs533511414	chr11:58680610-58680611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs140245327	chr11:58680637-58680638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs566703688	chr11:58680668-58680669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs531578	chr11:58680714-58680715	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs150295523	chr11:58680738-58680739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs191263375	chr11:58680769-58680770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs137947041	chr11:58680802-58680803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs115142514	chr11:58680867-58680868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs149530128	chr11:58680892-58680893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs374163031	chr11:58680916-58680917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs182541393	chr11:58680936-58680937	Weak transcription	n/a	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:2329 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:58673800-58682200	Weak transcription	NH-A	brain
2	chr11:58674000-58682200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr11:58674200-58679600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr11:58674200-58679600	Weak transcription	HMEC	breast
5	chr11:58674200-58682200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr11:58679200-58680200	Enhancers	NHEK	skin
7	chr11:58679400-58679800	Enhancers	Muscle Satellite Cultured Cells	--
8	chr11:58679600-58679800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr11:58679600-58680000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr11:58679600-58680000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr11:58679600-58680000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr11:58679600-58680000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr11:58679600-58680000	Enhancers	HMEC	breast
14	chr11:58679800-58682200	Weak transcription	Muscle Satellite Cultured Cells	--
15	chr11:58680000-58682000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr11:58680000-58682000	Weak transcription	HMEC	breast
17	chr11:58680000-58682200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr11:58680200-58681400	Weak transcription	NHEK	skin
19	chr11:58681000-58681800	Enhancers	Rectal Mucosa Donor 31	rectum
20	chr11:58681400-58683400	Enhancers	NHEK	skin
21	chr11:58682000-58682800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr11:58682000-58683400	Enhancers	HMEC	breast
23	chr11:58682200-58682800	Enhancers	Osteobl	bone
24	chr11:58682200-58683000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr11:58682200-58683000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr11:58682200-58683000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr11:58682200-58683000	Enhancers	NH-A	brain
28	chr11:58682200-58683200	Enhancers	Muscle Satellite Cultured Cells	--
29	chr11:58682200-58683200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr11:58682200-58683400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr11:58683000-58686800	Weak transcription	NH-A	brain
32	chr11:58683400-58690000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr11:58686200-58692600	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr11:58686600-58686800	Enhancers	Colonic Mucosa	Colon
35	chr11:58686600-58687200	ZNF genes & repeats	NHEK	skin
36	chr11:58686800-58687200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr11:58686800-58687600	Enhancers	NH-A	brain
38	chr11:58686800-58689200	Weak transcription	Colonic Mucosa	Colon
39	chr11:58687000-58687600	Enhancers	Muscle Satellite Cultured Cells	--
40	chr11:58687000-58687800	Enhancers	HMEC	breast
41	chr11:58687200-58687600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr11:58687200-58687600	Enhancers	HSMM	muscle
43	chr11:58687200-58687800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr11:58687200-58687800	Enhancers	Monocytes-CD14+_RO01746	blood
45	chr11:58687200-58688000	Enhancers	Fetal Thymus	thymus
46	chr11:58687200-58688200	Enhancers	Thymus	Thymus
47	chr11:58687200-58690400	Weak transcription	NHEK	skin
48	chr11:58687200-58690600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr11:58687200-58694800	Enhancers	Fetal Intestine Large	intestine
50	chr11:58687200-58694800	Enhancers	Fetal Intestine Small	intestine

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