Variant report

Variant	nsv524406
Chromosome Location	chr11:119873404-119893179
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	chr11:119884088-119884289	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr11:119886544-119886721	H1-hESC	embryonic stem cell:	n/a	chr11:119886628-119886639 chr11:119886630-119886641 chr11:119886628-119886641
8	CEBPB	chr11:119886515-119886784	IMR90	lung:	n/a	chr11:119886628-119886639 chr11:119886630-119886641 chr11:119886628-119886641
9	CEBPB	chr11:119876410-119876514	HepG2	liver:	n/a	n/a
10	CEBPB	chr11:119886597-119886715	Hela-S3	cervix:	n/a	chr11:119886628-119886639 chr11:119886630-119886641 chr11:119886628-119886641
11	CEBPB	chr11:119886569-119886769	K562	blood:	n/a	chr11:119886628-119886639 chr11:119886630-119886641 chr11:119886628-119886641
12	CEBPB	chr11:119886477-119886822	HepG2	liver:	n/a	chr11:119886628-119886639 chr11:119886630-119886641 chr11:119886628-119886641
13	CHD1	chr11:119873499-119873589	GM12878	blood:	n/a	n/a
14	CHD2	chr11:119883958-119884349	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr11:119884100-119884250	HCT-116	colon:	n/a	chr11:119884123-119884136
16	CTCF	chr11:119884015-119884194	SK-N-SH_RA	brain:	n/a	chr11:119884123-119884136
17	CTCF	chr11:119885820-119885970	GM12873	blood:	n/a	n/a
18	CTCF	chr11:119883951-119884280	K562	blood:	n/a	chr11:119884123-119884136
19	CTCF	chr11:119884100-119884250	GM12869	blood:	n/a	chr11:119884123-119884136
20	CTCF	chr11:119884062-119884214	GM13976	blood:	n/a	chr11:119884123-119884136
21	CTCF	chr11:119884060-119884210	BJ	skin:	n/a	chr11:119884123-119884136
22	CTCF	chr11:119884080-119884230	HA-sp	spinal cord:	n/a	chr11:119884123-119884136
23	CTCF	chr11:119883961-119884233	HepG2	liver:	n/a	chr11:119884123-119884136
24	CTCF	chr11:119883984-119884274	ProgFib	skin:	n/a	chr11:119884123-119884136
25	CTCF	chr11:119884060-119884210	HMEC	breast:	n/a	chr11:119884123-119884136
26	CTCF	chr11:119883977-119884262	K562	blood:	n/a	chr11:119884123-119884136
27	CTCF	chr11:119884060-119884210	WERI-Rb-1	eye:	n/a	chr11:119884123-119884136
28	CTCF	chr11:119884060-119884210	AG09309	skin:	n/a	chr11:119884123-119884136
29	CTCF	chr11:119883560-119883830	HAc	cerebellar:	n/a	n/a
30	CTCF	chr11:119884060-119884210	GM12864	blood:	n/a	chr11:119884123-119884136
31	CTCF	chr11:119884035-119884227	Spleen_OC	spleen:	n/a	chr11:119884123-119884136
32	CTCF	chr11:119883944-119884333	H1-hESC	embryonic stem cell:	n/a	chr11:119884123-119884136
33	CTCF	chr11:119884060-119884210	GM12868	blood:	n/a	chr11:119884123-119884136
34	CTCF	chr11:119884080-119884230	HCT-116	colon:	n/a	chr11:119884123-119884136
35	CTCF	chr11:119884080-119884230	HUVEC	blood vessel:	n/a	chr11:119884123-119884136
36	CTCF	chr11:119883968-119884279	MCF-7	breast:	n/a	chr11:119884123-119884136
37	CTCF	chr11:119883989-119884272	GM12878	blood:	n/a	chr11:119884123-119884136
38	CTCF	chr11:119884060-119884210	HMF	breast:	n/a	chr11:119884123-119884136
39	CTCF	chr11:119883976-119884282	GM19238	blood:	n/a	chr11:119884123-119884136
40	CTCF	chr11:119884080-119884230	GM12871	blood:	n/a	chr11:119884123-119884136
41	CTCF	chr11:119884080-119884230	HCPEpiC	choroid plexus:	n/a	chr11:119884123-119884136
42	CTCF	chr11:119883974-119884283	Fibrobl	skin:	n/a	chr11:119884123-119884136
43	CTCF	chr11:119884040-119884190	HepG2	liver:	n/a	chr11:119884123-119884136
44	CTCF	chr11:119884060-119884210	GM12867	blood:	n/a	chr11:119884123-119884136
45	CTCF	chr11:119884040-119884190	GM12872	blood:	n/a	chr11:119884123-119884136
46	CTCF	chr11:119884100-119884250	GM12864	blood:	n/a	chr11:119884123-119884136
47	CTCF	chr11:119884160-119884310	WI-38	lung:	n/a	n/a
48	CTCF	chr11:119884039-119884232	SK-N-SH_RA	brain:	n/a	chr11:119884123-119884136
49	CTCF	chr11:119884002-119884257	A549	lung:	n/a	chr11:119884123-119884136
50	CTCF	chr11:119883891-119884398	MCF-7	breast:	n/a	chr11:119884123-119884136

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:119881616-119881666	SAEC	small airway:	n/a
2	chr11:119881616-119881666	AG09319	gingival:	n/a
3	chr11:119887950-119888000	LNCaP	prostate:	n/a
4	chr11:119881616-119881666	SK-N-SH	brain:	n/a
5	chr11:119881616-119881666	H1-hESC	embryonic stem cell:	embryo
6	chr11:119887950-119888000	SK-N-SH	brain:	n/a
7	chr11:119887950-119888000	SK-N-MC	brain:	n/a
8	chr11:119881616-119881666	PrEC	prostate:	n/a
9	chr11:119887950-119888000	CMK	blood:	n/a
10	chr11:119887950-119888000	HPAEpiC	pulmonary alveolar:	n/a
11	chr11:119887950-119888000	NT2-D1	testis:	n/a
12	chr11:119887950-119888000	Hela-S3	cervix:	n/a
13	chr11:119887950-119888000	PANC-1	pancreas:	n/a
14	chr11:119887950-119888000	BE2_C	brain:	n/a
15	chr11:119881616-119881666	U87	brain:	n/a
16	chr11:119881616-119881666	HepG2	liver:	n/a
17	chr11:119887950-119888000	BJ	skin:	n/a
18	chr11:119881616-119881666	HMEC	breast:	n/a
19	chr11:119881616-119881666	ovcar-3	ovarian:	n/a
20	chr11:119881616-119881666	ProgFib	skin:	n/a
21	chr11:119881616-119881666	AG04449	skin:	fetal
22	chr11:119887950-119888000	NHDF-neo	bronchial:	n/a
23	chr11:119887950-119888000	GM19239	blood:	n/a
24	chr11:119881616-119881666	NHBE	bronchial:	n/a
25	chr11:119881616-119881666	HRPEpiC	eye:	n/a
26	chr11:119887950-119888000	HNPCEpiC	eye:	n/a
27	chr11:119887950-119888000	GM12891	blood:	n/a
28	chr11:119887950-119888000	U87	brain:	n/a
29	chr11:119887950-119888000	Jurkat	blood:	n/a
30	chr11:119881616-119881666	HRCEpiC	kidney:	n/a
31	chr11:119887950-119888000	SK-N-SH_RA	brain:	n/a
32	chr11:119881616-119881666	GM19239	blood:	n/a
33	chr11:119881616-119881666	PANC-1	pancreas:	n/a
34	chr11:119887950-119888000	NHBE	bronchial:	n/a
35	chr11:119887950-119888000	HL-60	blood:	n/a
36	chr11:119881616-119881666	GM12892	blood:	n/a
37	chr11:119881616-119881666	HEK293	kidney:	embryo
38	chr11:119887950-119888000	HEK293	kidney:	embryo
39	chr11:119887950-119888000	HRE	kidney:	n/a
40	chr11:119881616-119881666	CMK	blood:	n/a
41	chr11:119887950-119888000	PFSK-1	brain:	n/a
42	chr11:119887950-119888000	IMR90	lung:	fetal
43	chr11:119881616-119881666	K562	blood:	n/a
44	chr11:119881616-119881666	NB4	blood:	n/a
45	chr11:119881616-119881666	NHDF-neo	bronchial:	n/a
46	chr11:119881616-119881666	HCT-116	colon:	n/a
47	chr11:119881616-119881666	SK-N-SH_RA	brain:	n/a
48	chr11:119887950-119888000	HCM	heart:	n/a
49	chr11:119887950-119888000	ProgFib	skin:	n/a
50	chr11:119887950-119888000	PrEC	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:119893105..119894802-chr11:119896511..119898254,2	K562	blood:
2	chr11:119886138..119888688-chr11:119891563..119894396,2	K562	blood:
3	chr11:119536835..119537469-chr11:119883617..119884436,2	MCF-7	breast:
4	chr11:119883883..119884665-chr11:119978239..119979557,5	MCF-7	breast:
5	chr11:119865550..119868461-chr11:119874925..119876802,2	K562	blood:
6	chr11:119599746..119600613-chr11:119883658..119884285,2	MCF-7	breast:
7	chr11:119875923..119878520-chr11:119878673..119880916,2	K562	blood:
8	chr11:119536949..119537719-chr11:119883693..119884201,2	MCF-7	breast:
9	chr11:119875923..119878520-chr11:119878673..119880916,2	K562	blood:
10	chr11:119880494..119882883-chr11:119885315..119887974,2	K562	blood:
11	chr11:119881383..119883433-chr11:119886474..119889218,2	K562	blood:
12	chr11:119867354..119869206-chr11:119872754..119874804,2	K562	blood:
13	chr11:119600000..119600710-chr11:119883945..119884504,2	MCF-7	breast:
14	chr11:119886138..119888688-chr11:119891563..119894396,2	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
ENSG00000255216	chromatin interactions
ENSG00000110400	chromatin interactions
ENSG00000254854	chromatin interactions

Extended variants
information (count: 824 )
Associated
traits (count: 112 )

Variant overlapped rSNPs/rCNVs (count:824 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11217624	chr11:119873404-119873405	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs531843270	chr11:119873406-119873407	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs536011539	chr11:119873429-119873430	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs554823558	chr11:119873462-119873463	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs142915329	chr11:119873464-119873465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs535932639	chr11:119873497-119873498	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs368027820	chr11:119873519-119873520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs73586071	chr11:119873530-119873531	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs566134714	chr11:119873581-119873582	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs185715294	chr11:119873658-119873659	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs558596827	chr11:119873706-119873707	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs138207235	chr11:119873717-119873718	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs570711735	chr11:119873727-119873728	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs7106560	chr11:119873728-119873729	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs556323149	chr11:119873731-119873732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs574642367	chr11:119873794-119873795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs542343945	chr11:119873843-119873844	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs150364704	chr11:119873880-119873881	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs572486144	chr11:119873889-119873890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs546161605	chr11:119873899-119873900	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs371769295	chr11:119873913-119873914	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs74947477	chr11:119873995-119873996	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs12277627	chr11:119874030-119874031	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs377259824	chr11:119874100-119874101	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs11217625	chr11:119874170-119874171	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs114278496	chr11:119874212-119874213	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs373950958	chr11:119874220-119874221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs531947899	chr11:119874290-119874291	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs547905701	chr11:119874291-119874292	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs7929916	chr11:119874301-119874302	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs11217626	chr11:119874352-119874353	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs531866305	chr11:119874391-119874392	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs552131115	chr11:119874420-119874421	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs11217627	chr11:119874434-119874435	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs547474702	chr11:119874464-119874465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs117655883	chr11:119874497-119874498	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs556135393	chr11:119874530-119874531	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs369744555	chr11:119874538-119874539	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs535608808	chr11:119874594-119874595	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs190122338	chr11:119874603-119874604	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs138728300	chr11:119874608-119874609	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs60650014	chr11:119874621-119874622	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs558122952	chr11:119874634-119874635	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs58030968	chr11:119874653-119874654	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs183079877	chr11:119874663-119874664	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs544882789	chr11:119874679-119874680	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs370077935	chr11:119874692-119874693	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs187103009	chr11:119874744-119874745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs529462106	chr11:119874757-119874758	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs7126918	chr11:119874855-119874856	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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:197 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:119866400-119880200	Weak transcription	Esophagus	oesophagus
2	chr11:119870600-119873800	Enhancers	Brain Hippocampus Middle	brain
3	chr11:119871000-119877200	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr11:119871400-119873800	Enhancers	Brain Germinal Matrix	brain
5	chr11:119871600-119873600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr11:119872000-119873600	Enhancers	Brain Anterior Caudate	brain
7	chr11:119872200-119880200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr11:119872400-119873800	Enhancers	Fetal Kidney	kidney
9	chr11:119872800-119873600	Enhancers	Brain Angular Gyrus	brain
10	chr11:119873000-119875400	Weak transcription	HMEC	breast
11	chr11:119873200-119873600	Enhancers	Brain Inferior Temporal Lobe	brain
12	chr11:119873200-119875400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr11:119873600-119879200	Weak transcription	Brain Anterior Caudate	brain
14	chr11:119875200-119875600	Enhancers	Stomach Mucosa	stomach
15	chr11:119875400-119875600	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr11:119875400-119876200	Enhancers	HMEC	breast
17	chr11:119875400-119876400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr11:119875600-119880400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr11:119877200-119879600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr11:119878800-119879400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr11:119879200-119879400	Enhancers	Brain Anterior Caudate	brain
22	chr11:119879200-119879800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr11:119879400-119879800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr11:119879600-119889200	Enhancers	Breast Myoepithelial Primary Cells	Breast
25	chr11:119879800-119880200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr11:119879800-119881000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr11:119880000-119880800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr11:119880000-119880800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
29	chr11:119880200-119880400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr11:119880200-119880600	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
31	chr11:119880200-119880600	Weak transcription	Brain Cingulate Gyrus	brain
32	chr11:119880200-119880800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr11:119880200-119881000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr11:119880200-119881200	Bivalent Enhancer	Fetal Muscle Leg	muscle
35	chr11:119880200-119885000	Enhancers	Esophagus	oesophagus
36	chr11:119880400-119880600	Enhancers	Brain Germinal Matrix	brain
37	chr11:119880400-119881000	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr11:119880400-119884200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr11:119880600-119880800	Enhancers	H1 Cell Line	embryonic stem cell
40	chr11:119880600-119880800	Enhancers	Brain Anterior Caudate	brain
41	chr11:119880600-119880800	Enhancers	Brain Cingulate Gyrus	brain
42	chr11:119880600-119881000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
43	chr11:119880600-119881800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr11:119880600-119881800	Weak transcription	Brain Germinal Matrix	brain
45	chr11:119880800-119881000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
46	chr11:119880800-119881000	Enhancers	Right Ventricle	heart
47	chr11:119880800-119881200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr11:119880800-119881800	Weak transcription	Brain Anterior Caudate	brain
49	chr11:119880800-119881800	Weak transcription	Brain Cingulate Gyrus	brain
50	chr11:119880800-119883800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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