Variant report

Variant	esv2762948
Chromosome Location	chr11:119876596-119901422
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr11:119883865-119884317	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr11:119883955-119884284	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr11:119884035-119884235	K562	blood:	n/a	n/a
4	BRCA1	chr11:119884084-119884362	H1-hESC	embryonic stem cell:	n/a	n/a
5	BRCA1	chr11:119887432-119887433	HepG2	liver:	n/a	n/a
6	CEBPB	chr11:119886515-119886784	IMR90	lung:	n/a	chr11:119886628-119886639 chr11:119886630-119886641 chr11:119886628-119886641
7	CEBPB	chr11:119886477-119886822	HepG2	liver:	n/a	chr11:119886628-119886639 chr11:119886630-119886641 chr11:119886628-119886641
8	CEBPB	chr11:119886569-119886769	K562	blood:	n/a	chr11:119886628-119886639 chr11:119886630-119886641 chr11:119886628-119886641
9	CEBPB	chr11:119884088-119884289	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr11:119886544-119886721	H1-hESC	embryonic stem cell:	n/a	chr11:119886628-119886639 chr11:119886630-119886641 chr11:119886628-119886641
11	CEBPB	chr11:119886597-119886715	Hela-S3	cervix:	n/a	chr11:119886628-119886639 chr11:119886630-119886641 chr11:119886628-119886641
12	CHD2	chr11:119883958-119884349	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr11:119884060-119884210	RPTEC	kidney:	n/a	chr11:119884123-119884136
14	CTCF	chr11:119884040-119884190	HCFaa	heart:	n/a	chr11:119884123-119884136
15	CTCF	chr11:119883840-119883990	HCM	heart:	n/a	n/a
16	CTCF	chr11:119884080-119884230	SK-N-SH_RA	brain:	n/a	chr11:119884123-119884136
17	CTCF	chr11:119884060-119884210	HEK293	kidney:	n/a	chr11:119884123-119884136
18	CTCF	chr11:119883911-119884372	H1-hESC	embryonic stem cell:	n/a	chr11:119884123-119884136
19	CTCF	chr11:119897243-119897253	Kidney_OC	kidney:	n/a	n/a
20	CTCF	chr11:119884180-119884330	A549	lung:	n/a	n/a
21	CTCF	chr11:119883944-119884333	H1-hESC	embryonic stem cell:	n/a	chr11:119884123-119884136
22	CTCF	chr11:119884120-119884270	HFF-Myc	foreskin:	n/a	chr11:119884123-119884136
23	CTCF	chr11:119884100-119884250	NHLF	lung:	n/a	chr11:119884123-119884136
24	CTCF	chr11:119883968-119884279	MCF-7	breast:	n/a	chr11:119884123-119884136
25	CTCF	chr11:119884100-119884250	GM12864	blood:	n/a	chr11:119884123-119884136
26	CTCF	chr11:119884080-119884230	MCF-7	breast:	n/a	chr11:119884123-119884136
27	CTCF	chr11:119883976-119884282	GM19238	blood:	n/a	chr11:119884123-119884136
28	CTCF	chr11:119884080-119884230	HAc	cerebellar:	n/a	chr11:119884123-119884136
29	CTCF	chr11:119884080-119884230	GM12868	blood:	n/a	chr11:119884123-119884136
30	CTCF	chr11:119884040-119884190	GM12874	blood:	n/a	chr11:119884123-119884136
31	CTCF	chr11:119884060-119884210	SAEC	small airway:	n/a	chr11:119884123-119884136
32	CTCF	chr11:119883951-119884280	K562	blood:	n/a	chr11:119884123-119884136
33	CTCF	chr11:119884100-119884250	GM12801	blood:	n/a	chr11:119884123-119884136
34	CTCF	chr11:119883801-119884476	A549	lung:	n/a	chr11:119884123-119884136
35	CTCF	chr11:119884060-119884210	NHEK	skin:	n/a	chr11:119884123-119884136
36	CTCF	chr11:119884040-119884190	SK-N-SH_RA	brain:	n/a	chr11:119884123-119884136
37	CTCF	chr11:119884061-119884256	Lung_OC	lung:	n/a	chr11:119884123-119884136
38	CTCF	chr11:119883986-119884280	GM12892	blood:	n/a	chr11:119884123-119884136
39	CTCF	chr11:119884060-119884210	GM12865	blood:	n/a	chr11:119884123-119884136
40	CTCF	chr11:119884060-119884210	HVMF	connective:	n/a	chr11:119884123-119884136
41	CTCF	chr11:119884060-119884210	HCPEpiC	choroid plexus:	n/a	chr11:119884123-119884136
42	CTCF	chr11:119883609-119884524	SK-N-SH	brain:	n/a	chr11:119884123-119884136
43	CTCF	chr11:119884080-119884230	GM12869	blood:	n/a	chr11:119884123-119884136
44	CTCF	chr11:119883971-119884273	Medullo	brain:	n/a	chr11:119884123-119884136
45	CTCF	chr11:119884100-119884250	HFF-Myc	foreskin:	n/a	chr11:119884123-119884136
46	CTCF	chr11:119883841-119884443	HCT-116	colon:	n/a	chr11:119884123-119884136
47	CTCF	chr11:119884060-119884210	HRE	kidney:	n/a	chr11:119884123-119884136
48	CTCF	chr11:119884035-119884227	Spleen_OC	spleen:	n/a	chr11:119884123-119884136
49	CTCF	chr11:119884060-119884210	HepG2	liver:	n/a	chr11:119884123-119884136
50	CTCF	chr11:119885820-119885970	GM12873	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:119897708-119897758	ovcar-3	ovarian:	n/a
2	chr11:119897638-119897688	GM06990	blood:	n/a
3	chr11:119897708-119897758	ovcar-3	ovarian:	n/a
4	chr11:119897638-119897688	GM06990	blood:	n/a
5	chr11:119897638-119897688	Hela-S3	cervix:	n/a
6	chr11:119897638-119897688	SK-N-SH	brain:	n/a
7	chr11:119897708-119897758	HepG2	liver:	n/a
8	chr11:119887950-119888000	NT2-D1	testis:	n/a
9	chr11:119893672-119893722	A549	lung:	n/a
10	chr11:119881616-119881666	Hepatocyte	liver:	n/a
11	chr11:119897638-119897688	HIPEpiC	eye:	n/a
12	chr11:119893672-119893722	NHBE	bronchial:	n/a
13	chr11:119881616-119881666	HCT-116	colon:	n/a
14	chr11:119897638-119897688	AG04450	lung:	fetal
15	chr11:119887950-119888000	HepG2	liver:	n/a
16	chr11:119897638-119897688	HL-60	blood:	n/a
17	chr11:119887950-119888000	ECC-1	luminal epithelium:	n/a
18	chr11:119897708-119897758	NB4	blood:	n/a
19	chr11:119881616-119881666	LNCaP	prostate:	n/a
20	chr11:119897638-119897688	SK-N-MC	brain:	n/a
21	chr11:119897708-119897758	T-47D	breast:	n/a
22	chr11:119893672-119893722	H1-hESC	embryonic stem cell:	embryo
23	chr11:119897638-119897688	AG04449	skin:	fetal
24	chr11:119897708-119897758	PrEC	prostate:	n/a
25	chr11:119897708-119897758	HUVEC	blood vessel:	n/a
26	chr11:119887950-119888000	HUVEC	blood vessel:	n/a
27	chr11:119897638-119897688	SK-N-SH_RA	brain:	n/a
28	chr11:119881616-119881666	HCF	heart:	n/a
29	chr11:119897638-119897688	HepG2	liver:	n/a
30	chr11:119893672-119893722	Jurkat	blood:	n/a
31	chr11:119893672-119893722	U87	brain:	n/a
32	chr11:119881616-119881666	GM19239	blood:	n/a
33	chr11:119887950-119888000	HRPEpiC	eye:	n/a
34	chr11:119893672-119893722	SK-N-MC	brain:	n/a
35	chr11:119897638-119897688	HEK293	kidney:	embryo
36	chr11:119897708-119897758	AG04449	skin:	fetal
37	chr11:119897708-119897758	H1-hESC	embryonic stem cell:	embryo
38	chr11:119897708-119897758	HCPEpiC	choroid plexus:	n/a
39	chr11:119881616-119881666	HRPEpiC	eye:	n/a
40	chr11:119881616-119881666	Jurkat	blood:	n/a
41	chr11:119887950-119888000	CMK	blood:	n/a
42	chr11:119887950-119888000	Hepatocyte	liver:	n/a
43	chr11:119897638-119897688	HCF	heart:	n/a
44	chr11:119881616-119881666	SK-N-SH_RA	brain:	n/a
45	chr11:119887950-119888000	A549	lung:	n/a
46	chr11:119897708-119897758	SK-N-SH_RA	brain:	n/a
47	chr11:119881616-119881666	AG04449	skin:	fetal
48	chr11:119887950-119888000	BJ	skin:	n/a
49	chr11:119881616-119881666	U87	brain:	n/a
50	chr11:119897638-119897688	A549	lung:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:119898837..119900812-chr11:119902975..119904748,2	K562	blood:
2	chr11:119536835..119537469-chr11:119883617..119884436,2	MCF-7	breast:
3	chr11:119880494..119882883-chr11:119885315..119887974,2	K562	blood:
4	chr11:119893105..119894802-chr11:119896511..119898254,2	K562	blood:
5	chr11:119600000..119600710-chr11:119883945..119884504,2	MCF-7	breast:
6	chr11:119865550..119868461-chr11:119874925..119876802,2	K562	blood:
7	chr11:119886138..119888688-chr11:119891563..119894396,2	K562	blood:
8	chr11:119893105..119894802-chr11:119896511..119898254,2	K562	blood:
9	chr11:119881383..119883433-chr11:119886474..119889218,2	K562	blood:
10	chr11:119886138..119888688-chr11:119891563..119894396,2	K562	blood:
11	chr11:119599746..119600613-chr11:119883658..119884285,2	MCF-7	breast:
12	chr11:119536949..119537719-chr11:119883693..119884201,2	MCF-7	breast:
13	chr11:119883883..119884665-chr11:119978239..119979557,5	MCF-7	breast:
14	chr11:119875923..119878520-chr11:119878673..119880916,2	K562	blood:
15	chr11:119875923..119878520-chr11:119878673..119880916,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-831A10.1.1-2	chr11:119882802-119882867	ENSG00000255216.1
2	lnc-RP11-831A10.1.1-2	chr11:119879313-119879808	ENSG00000255216.1

Variant related genes	Relation type
ENSG00000255216	TF binding region
ENSG00000255216	CpG island
ENSG00000254863	chromatin interactions
ENSG00000110400	chromatin interactions
ENSG00000255216	chromatin interactions
ENSG00000254854	chromatin interactions

Extended variants
information (count: 1047 )
Associated
traits (count: 112 )

Variant overlapped rSNPs/rCNVs (count:1047 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs557261815	chr11:119876633-119876634	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs17311121	chr11:119876680-119876681	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs142083351	chr11:119876688-119876689	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs4938750	chr11:119876697-119876698	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs573695036	chr11:119876704-119876705	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs72645477	chr11:119876760-119876761	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs11825700	chr11:119876761-119876762	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs144277400	chr11:119876776-119876777	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs545231614	chr11:119876806-119876807	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs563348933	chr11:119876814-119876815	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs575014531	chr11:119876820-119876821	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs530574520	chr11:119876821-119876822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs542142811	chr11:119876822-119876823	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs75160858	chr11:119876827-119876828	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs572343257	chr11:119876867-119876868	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs545996306	chr11:119876878-119876879	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs567404465	chr11:119876901-119876902	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs191830374	chr11:119876911-119876912	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs183905022	chr11:119876917-119876918	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs546673267	chr11:119876927-119876928	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs147825095	chr11:119876937-119876938	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs538971768	chr11:119876938-119876939	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs4938751	chr11:119876939-119876940	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs569494283	chr11:119876960-119876961	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs536808880	chr11:119876969-119876970	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs141293762	chr11:119876983-119876984	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs550271776	chr11:119876984-119876985	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs562539953	chr11:119877007-119877008	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs573758954	chr11:119877045-119877046	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs4938752	chr11:119877101-119877102	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs190418429	chr11:119877106-119877107	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs4938753	chr11:119877108-119877109	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs544980944	chr11:119877116-119877117	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs192882635	chr11:119877119-119877120	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs575127062	chr11:119877146-119877147	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs143547234	chr11:119877156-119877157	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs148073402	chr11:119877193-119877194	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs528554690	chr11:119877202-119877203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs4938754	chr11:119877246-119877247	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs570831386	chr11:119877247-119877248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs373387963	chr11:119877300-119877301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs535521169	chr11:119877315-119877316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs538354356	chr11:119877358-119877359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs532508520	chr11:119877371-119877372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs556260197	chr11:119877393-119877394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs572131814	chr11:119877397-119877398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs569556768	chr11:119877418-119877419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs377547320	chr11:119877502-119877503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs548799010	chr11:119877506-119877507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs567410443	chr11:119877513-119877514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:112)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	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
Cancer	22429812	CNVD
Breast cancer	16608533	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21364760	CNVD
Mental retardation	19966786	CNVD
Non-small cell lung cancer	21829676	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Ovarian cancer	21720365	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Neuroblastoma	17327916	CNVD
Malignant melanoma	17260012	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Renal cell carcinoma	21668985	CNVD
Developmental delay	21147756	CNVD
Emanuel syndrome	21549014	CNVD
Emanuel syndrome	18184694	CNVD
Non-syndromic sensorineural hearing loss	18184694	CNVD
Acute lymphoblastic leukemia	22581003	CNVD
Ovarian neoplasms	16753589	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cancer	21183584	CNVD
Retinoblastoma	22278416	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-syndromic sensorineural hearing loss	16829213	CNVD
Non-syndromic sensorineural hearing loss	16760666	CNVD
Squamous cell cancer	20885788	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Neurocytoma	17123091	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Central neurocytomas	17123091	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Hepatocellular carcinoma	16750200	CNVD
Multiple myeloma	17550852	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Acute myeloid leukemia	19651601	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	20409316	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Heart disease	20551144	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Autism	22543975	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	21509527	CNVD
Ductal carcinoma	22052326	CNVD
Schizophrenia	23813976	CNVD
Cancer	17440070	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:242 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:119866400-119880200	Weak transcription	Esophagus	oesophagus
2	chr11:119871000-119877200	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr11:119872200-119880200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr11:119873600-119879200	Weak transcription	Brain Anterior Caudate	brain
5	chr11:119875600-119880400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr11:119877200-119879600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr11:119878800-119879400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr11:119879200-119879400	Enhancers	Brain Anterior Caudate	brain
9	chr11:119879200-119879800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr11:119879400-119879800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr11:119879600-119889200	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr11:119879800-119880200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr11:119879800-119881000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr11:119880000-119880800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr11:119880000-119880800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
16	chr11:119880200-119880400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr11:119880200-119880600	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
18	chr11:119880200-119880600	Weak transcription	Brain Cingulate Gyrus	brain
19	chr11:119880200-119880800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr11:119880200-119881000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr11:119880200-119881200	Bivalent Enhancer	Fetal Muscle Leg	muscle
22	chr11:119880200-119885000	Enhancers	Esophagus	oesophagus
23	chr11:119880400-119880600	Enhancers	Brain Germinal Matrix	brain
24	chr11:119880400-119881000	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr11:119880400-119884200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr11:119880600-119880800	Enhancers	H1 Cell Line	embryonic stem cell
27	chr11:119880600-119880800	Enhancers	Brain Anterior Caudate	brain
28	chr11:119880600-119880800	Enhancers	Brain Cingulate Gyrus	brain
29	chr11:119880600-119881000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
30	chr11:119880600-119881800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
31	chr11:119880600-119881800	Weak transcription	Brain Germinal Matrix	brain
32	chr11:119880800-119881000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
33	chr11:119880800-119881000	Enhancers	Right Ventricle	heart
34	chr11:119880800-119881200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr11:119880800-119881800	Weak transcription	Brain Anterior Caudate	brain
36	chr11:119880800-119881800	Weak transcription	Brain Cingulate Gyrus	brain
37	chr11:119880800-119883800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr11:119880800-119884800	Enhancers	Brain Substantia Nigra	brain
39	chr11:119881000-119883200	Weak transcription	Right Ventricle	heart
40	chr11:119881200-119882000	Enhancers	Fetal Muscle Leg	muscle
41	chr11:119881200-119884600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr11:119881400-119882000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
43	chr11:119881400-119884400	Enhancers	Brain Hippocampus Middle	brain
44	chr11:119881600-119881800	Enhancers	Fetal Thymus	thymus
45	chr11:119881600-119885800	Enhancers	Brain Inferior Temporal Lobe	brain
46	chr11:119881800-119882600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr11:119881800-119884000	Enhancers	Brain Anterior Caudate	brain
48	chr11:119881800-119884000	Weak transcription	Fetal Thymus	thymus
49	chr11:119881800-119884800	Enhancers	Brain Germinal Matrix	brain
50	chr11:119881800-119890000	Enhancers	Brain Cingulate Gyrus	brain

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