Variant report

Variant	nsv556216
Chromosome Location	chr11:104333651-104560789
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1087)
CpG islands
(count:245)
Chromatin interactive
region (count:15)
LncRNA
region (count:22)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1087 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:104539807-104540209	HepG2	liver:	n/a	n/a
2	BACH1	chr11:104404978-104405409	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL11A	chr11:104452026-104452271	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL11A	chr11:104451956-104452294	H1-hESC	embryonic stem cell:	n/a	n/a
5	BRCA1	chr11:104336495-104336518	Hela-S3	cervix:	n/a	n/a
6	CBX3	chr11:104539778-104540232	HCT-116	colon:	n/a	n/a
7	CBX3	chr11:104520974-104521253	HCT-116	colon:	n/a	n/a
8	CEBPB	chr11:104508427-104509111	Hela-S3	cervix:	n/a	chr11:104508922-104508933
9	CEBPB	chr11:104534113-104534393	IMR90	lung:	n/a	chr11:104534205-104534216
10	CEBPB	chr11:104404965-104405432	IMR90	lung:	n/a	n/a
11	CEBPB	chr11:104539817-104540111	HepG2	liver:	n/a	n/a
12	CEBPB	chr11:104525090-104525327	K562	blood:	n/a	chr11:104525181-104525194 chr11:104525181-104525194 chr11:104525181-104525194 chr11:104525181-104525192
13	CEBPB	chr11:104525026-104525358	IMR90	lung:	n/a	chr11:104525322-104525333 chr11:104525181-104525194 chr11:104525181-104525194 chr11:104525181-104525194 chr11:104525181-104525192
14	CEBPB	chr11:104440984-104441394	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr11:104335721-104335846	HepG2	liver:	n/a	chr11:104335766-104335777
16	CEBPB	chr11:104534104-104534298	HepG2	liver:	n/a	chr11:104534205-104534216
17	CEBPB	chr11:104418775-104419061	A549	lung:	n/a	chr11:104418932-104418943
18	CEBPB	chr11:104494198-104494575	IMR90	lung:	n/a	chr11:104494285-104494296 chr11:104494285-104494296
19	CEBPB	chr11:104512599-104512892	HepG2	liver:	n/a	chr11:104512746-104512757
20	CEBPB	chr11:104365015-104365286	IMR90	lung:	n/a	n/a
21	CEBPB	chr11:104444090-104444528	Hela-S3	cervix:	n/a	chr11:104444139-104444152
22	CEBPB	chr11:104418796-104419073	Hela-S3	cervix:	n/a	chr11:104418932-104418943
23	CEBPB	chr11:104365000-104365259	HepG2	liver:	n/a	n/a
24	CEBPB	chr11:104539774-104540189	IMR90	lung:	n/a	n/a
25	CEBPB	chr11:104550013-104550355	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr11:104536453-104536685	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr11:104539824-104540164	A549	lung:	n/a	n/a
28	CEBPB	chr11:104474320-104474546	A549	lung:	n/a	chr11:104474423-104474434
29	CEBPB	chr11:104525013-104525262	A549	lung:	n/a	chr11:104525181-104525194 chr11:104525181-104525194 chr11:104525181-104525194 chr11:104525181-104525192
30	CEBPB	chr11:104418823-104419081	HepG2	liver:	n/a	chr11:104418932-104418943
31	CEBPB	chr11:104539759-104540264	A549	lung:	n/a	n/a
32	CEBPB	chr11:104537084-104537209	H1-hESC	embryonic stem cell:	n/a	chr11:104537185-104537196
33	CEBPB	chr11:104474275-104474597	HepG2	liver:	n/a	chr11:104474423-104474434
34	CEBPB	chr11:104539749-104540204	HCT-116	colon:	n/a	n/a
35	CEBPB	chr11:104335648-104335888	A549	lung:	n/a	chr11:104335766-104335777
36	CEBPB	chr11:104452414-104452693	IMR90	lung:	n/a	chr11:104452534-104452547
37	CEBPB	chr11:104341857-104341865	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr11:104365021-104365243	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr11:104539700-104540315	HCT-116	colon:	n/a	n/a
40	CEBPB	chr11:104539680-104540284	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr11:104537036-104537358	HepG2	liver:	n/a	chr11:104537185-104537196
42	CEBPB	chr11:104365047-104365362	A549	lung:	n/a	n/a
43	CEBPB	chr11:104355702-104355911	HepG2	liver:	n/a	chr11:104355849-104355860
44	CEBPB	chr11:104481416-104481629	HepG2	liver:	n/a	chr11:104481550-104481558 chr11:104481467-104481478
45	CEBPB	chr11:104480012-104480256	H1-hESC	embryonic stem cell:	n/a	chr11:104480194-104480207
46	CEBPB	chr11:104536365-104536737	IMR90	lung:	n/a	n/a
47	CEBPB	chr11:104418754-104419111	IMR90	lung:	n/a	chr11:104418932-104418943
48	CEBPB	chr11:104479994-104480282	Hela-S3	cervix:	n/a	chr11:104480194-104480207
49	CEBPB	chr11:104489254-104489482	HepG2	liver:	n/a	n/a
50	CEBPB	chr11:104442981-104443405	Hela-S3	cervix:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:104508637-104508687	ovcar-3	ovarian:	n/a
2	chr11:104508637-104508687	ovcar-3	ovarian:	n/a
3	chr11:104435867-104435917	PFSK-1	brain:	n/a
4	chr11:104508637-104508687	SK-N-SH_RA	brain:	n/a
5	chr11:104405198-104405248	CMK	blood:	n/a
6	chr11:104435867-104435917	HPAEpiC	pulmonary alveolar:	n/a
7	chr11:104435867-104435917	GM12891	blood:	n/a
8	chr11:104435867-104435917	HCPEpiC	choroid plexus:	n/a
9	chr11:104435867-104435917	NH-A	brain:	n/a
10	chr11:104405198-104405248	U87	brain:	n/a
11	chr11:104508637-104508687	NHDF-neo	bronchial:	n/a
12	chr11:104435867-104435917	GM12892	blood:	n/a
13	chr11:104501066-104501116	AoSMC	blood vessel:	n/a
14	chr11:104405198-104405248	GM12892	blood:	n/a
15	chr11:104405198-104405248	GM19239	blood:	n/a
16	chr11:104508637-104508687	PFSK-1	brain:	n/a
17	chr11:104501066-104501116	HCM	heart:	n/a
18	chr11:104508637-104508687	HUVEC	blood vessel:	n/a
19	chr11:104508637-104508687	BE2_C	brain:	n/a
20	chr11:104405198-104405248	SK-N-SH_RA	brain:	n/a
21	chr11:104405198-104405248	HCT-116	colon:	n/a
22	chr11:104405198-104405248	NT2-D1	testis:	n/a
23	chr11:104501066-104501116	K562	blood:	n/a
24	chr11:104508637-104508687	HCT-116	colon:	n/a
25	chr11:104435867-104435917	MCF-7	breast:	n/a
26	chr11:104435867-104435917	K562	blood:	n/a
27	chr11:104501066-104501116	HNPCEpiC	eye:	n/a
28	chr11:104405198-104405248	RPTEC	kidney:	n/a
29	chr11:104508637-104508687	SK-N-MC	brain:	n/a
30	chr11:104501066-104501116	PrEC	prostate:	n/a
31	chr11:104501066-104501116	T-47D	breast:	n/a
32	chr11:104501066-104501116	ProgFib	skin:	n/a
33	chr11:104435867-104435917	ovcar-3	ovarian:	n/a
34	chr11:104501066-104501116	A549	lung:	n/a
35	chr11:104405198-104405248	MCF10A-Er-Src	breast:	n/a
36	chr11:104508637-104508687	BJ	skin:	n/a
37	chr11:104508637-104508687	HepG2	liver:	n/a
38	chr11:104405198-104405248	SK-N-MC	brain:	n/a
39	chr11:104405198-104405248	AG09309	skin:	n/a
40	chr11:104405198-104405248	HEEpiC	esophagus:	n/a
41	chr11:104508637-104508687	HAEpiC	amniotic membrane:	n/a
42	chr11:104405198-104405248	IMR90	lung:	fetal
43	chr11:104435867-104435917	IMR90	lung:	fetal
44	chr11:104435867-104435917	HRE	kidney:	n/a
45	chr11:104405198-104405248	Caco-2	colon:	n/a
46	chr11:104405198-104405248	Jurkat	blood:	n/a
47	chr11:104501066-104501116	Hela-S3	cervix:	n/a
48	chr11:104435867-104435917	HRCEpiC	kidney:	n/a
49	chr11:104435867-104435917	PrEC	prostate:	n/a
50	chr11:104501066-104501116	AG10803	skin:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:104481943..104484005-chr11:104508194..104510818,2	K562	blood:
2	chr11:104516723..104519201-chr11:104522234..104524667,2	K562	blood:
3	chr11:104377912..104380713-chr11:104411485..104413500,2	MCF-7	breast:
4	chr11:104331867..104333415-chr11:104336822..104339133,2	K562	blood:
5	chr11:104377912..104380713-chr11:104411485..104413500,2	MCF-7	breast:
6	chr11:104380583..104383114-chr11:104384527..104386564,2	K562	blood:
7	chr11:104505386..104506145-chr7:1705158..1706031,2	MCF-7	breast:
8	chr11:104242893..104244741-chr11:104376136..104378191,2	K562	blood:
9	chr11:104481697..104482494-chr17:63790105..63790828,2	MCF-7	breast:
10	chr11:104372355..104372989-chr5:37799043..37799937,2	MCF-7	breast:
11	chr11:104380583..104383114-chr11:104384527..104386564,2	K562	blood:
12	chr11:104516723..104519201-chr11:104522234..104524667,2	K562	blood:
13	chr11:104524242..104527061-chr11:104559725..104562588,2	K562	blood:
14	chr11:104481943..104484005-chr11:104508194..104510818,2	K562	blood:
15	chr11:104524242..104527061-chr11:104559725..104562588,2	K562	blood:

(count:22 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CASP12-1	chr11:104415604-104415877	ENSG00000256422
2	lnc-CASP12-1	chr11:104443285-104443325	ENSG00000256422
3	lnc-CASP12-1	chr11:104479965-104480030	ENSG00000256422
4	lnc-CASP12-1	chr11:104439776-104439859	ENSG00000256422
5	lnc-CASP12-1	chr11:104439776-104439859	NONHSAT023934
6	lnc-CASP12-1	chr11:104415427-104415514	ENSG00000256422
7	lnc-CASP12-1	chr11:104439083-104439649	XLOC_009538
8	lnc-CASP12-1	chr11:104415427-104415514	ENSG00000256422
9	lnc-CASP12-1	chr11:104442804-104443213	NONHSAT023935
10	lnc-CASP12-1	chr11:104410659-104410753	ENSG00000256422
11	lnc-CASP12-1	chr11:104479965-104480062	XLOC_009538
12	lnc-CASP12-1	chr11:104382877-104382961	ENSG00000256422
13	lnc-CASP12-1	chr11:104415604-104415877	ENSG00000256422
14	lnc-CASP12-1	chr11:104479965-104480102	NONHSAT023934
15	lnc-CASP12-1	chr11:104439221-104439649	NONHSAT023934
16	lnc-CASP12-1	chr11:104439776-104439859	XLOC_009538
17	lnc-CASP12-1	chr11:104439258-104439649	ENSG00000256422
18	lnc-CASP12-1	chr11:104439240-104439649	NONHSAT023935
19	lnc-CASP12-1	chr11:104443285-104443325	XLOC_009538
20	lnc-CASP12-1	chr11:104479965-104480049	ENSG00000256422
21	lnc-CASP12-1	chr11:104439776-104439859	NONHSAT023935
22	lnc-CASP12-1	chr11:104479965-104480024	ENSG00000256422

No data

Variant related genes	Relation type
ENSG00000270449	TF binding region
ENSG00000256422	TF binding region
ENSG00000270449	CpG island
ENSG00000256422	CpG island

Extended variants
information (count: 6314 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:6314 , 50 per page) page: 1 2 3 4 5 6 7 ... 127

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1906308	chr11:104333651-104333652	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs537686916	chr11:104333686-104333687	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs187175476	chr11:104333717-104333718	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs566093195	chr11:104333756-104333757	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs386757078	chr11:104333757-104333758	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs6591082	chr11:104333759-104333760	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs192442849	chr11:104333765-104333766	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs573452870	chr11:104333808-104333809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs545389983	chr11:104333813-104333814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs150726248	chr11:104333833-104333834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs531633963	chr11:104333854-104333855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs76389264	chr11:104333858-104333859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs568145167	chr11:104333896-104333897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs531103927	chr11:104333900-104333901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs551242619	chr11:104333957-104333958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs139022163	chr11:104333966-104333967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs554767538	chr11:104333984-104333985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs546928187	chr11:104333985-104333986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs566775464	chr11:104334005-104334006	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs145318098	chr11:104334046-104334047	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs184417586	chr11:104334097-104334098	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs190456577	chr11:104334128-104334129	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs200422802	chr11:104334134-104334135	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs7925886	chr11:104334149-104334150	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs574435872	chr11:104334182-104334183	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs147217785	chr11:104334190-104334191	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs543645034	chr11:104334199-104334200	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs374043395	chr11:104334209-104334210	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs193227099	chr11:104334213-104334214	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs545810103	chr11:104334232-104334233	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs11226373	chr11:104334239-104334240	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
32	rs184351991	chr11:104334251-104334252	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs371949659	chr11:104334259-104334260	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs561469168	chr11:104334269-104334270	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs530182036	chr11:104334293-104334294	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs7944328	chr11:104334328-104334329	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs188782283	chr11:104334345-104334346	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs369965647	chr11:104334360-104334361	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs552202607	chr11:104334383-104334384	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs536826666	chr11:104334394-104334395	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs568804592	chr11:104334437-104334438	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs531513506	chr11:104334451-104334452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs71484361	chr11:104334486-104334487	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs547951054	chr11:104334492-104334493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs568177097	chr11:104334499-104334500	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs534024052	chr11:104334510-104334511	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs114380494	chr11:104334551-104334552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs570573642	chr11:104334557-104334558	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs11825725	chr11:104334564-104334565	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs556202669	chr11:104334670-104334671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	20729466	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
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	22429812	CNVD
Breast cancer	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17603634	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	16790693	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Mental retardation	19966786	CNVD
Non-small cell lung cancer	21829676	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Intracranial aneurysm	16715129	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Ovarian cancer	21720365	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Neuroblastoma	17327916	CNVD
Melanoma	17363583	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Mantle cell lymphoma	19029149	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant melanoma	17260012	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Prostate cancer	16573809	CNVD
Obesity	19966786	CNVD
Tetralogy of Fallot	22912587	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:709 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:104323800-104334000	Weak transcription	Fetal Heart	heart
2	chr11:104333000-104333800	Enhancers	Muscle Satellite Cultured Cells	--
3	chr11:104333600-104333800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr11:104333800-104336200	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr11:104334000-104334600	Enhancers	Fetal Heart	heart
6	chr11:104335000-104335800	Enhancers	Fetal Muscle Leg	muscle
7	chr11:104336200-104336600	Enhancers	Muscle Satellite Cultured Cells	--
8	chr11:104336200-104336800	Enhancers	Cortex derived primary cultured neurospheres	brain
9	chr11:104336600-104336800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr11:104336600-104337000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr11:104336600-104338200	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr11:104336800-104338000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr11:104338000-104339600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr11:104338200-104338400	Enhancers	Muscle Satellite Cultured Cells	--
15	chr11:104338200-104338600	Enhancers	Dnd41	blood
16	chr11:104338200-104338600	Enhancers	HSMMtube	muscle
17	chr11:104340400-104340800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr11:104342200-104342600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr11:104342200-104342600	Enhancers	NHEK	skin
20	chr11:104344800-104345000	Enhancers	Ovary	ovary
21	chr11:104345200-104346800	Weak transcription	Ovary	ovary
22	chr11:104345800-104346000	Enhancers	Stomach Mucosa	stomach
23	chr11:104346000-104346600	Weak transcription	Stomach Mucosa	stomach
24	chr11:104346600-104347200	Enhancers	Stomach Mucosa	stomach
25	chr11:104346800-104347200	Enhancers	Ovary	ovary
26	chr11:104347000-104347600	Enhancers	Muscle Satellite Cultured Cells	--
27	chr11:104347200-104348400	Weak transcription	Stomach Mucosa	stomach
28	chr11:104347200-104357800	Weak transcription	Ovary	ovary
29	chr11:104348400-104348600	Enhancers	Stomach Mucosa	stomach
30	chr11:104348400-104349200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr11:104355600-104355800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr11:104355600-104357000	Enhancers	Fetal Lung	lung
33	chr11:104355600-104358400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr11:104356000-104356200	Enhancers	Brain Germinal Matrix	brain
35	chr11:104356400-104356800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr11:104356400-104357400	Weak transcription	Brain Germinal Matrix	brain
37	chr11:104356600-104358200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr11:104356800-104357200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr11:104357000-104357800	Weak transcription	Fetal Lung	lung
40	chr11:104357200-104358400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr11:104357200-104358400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr11:104357400-104358400	Enhancers	Brain Germinal Matrix	brain
43	chr11:104357600-104358000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr11:104357600-104359600	Enhancers	Fetal Heart	heart
45	chr11:104357800-104358000	Enhancers	Ovary	ovary
46	chr11:104357800-104358400	Enhancers	Fetal Lung	lung
47	chr11:104357800-104358600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
48	chr11:104358200-104358600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr11:104358200-104358600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr11:104358400-104358800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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