Variant report

Variant	esv2761706
Chromosome Location	chr11:104523335-104634024
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:410)
CpG islands
(count:122)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:410 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

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	ATF2	chr11:104576262-104577023	GM12878	blood:	n/a	n/a
3	BATF	chr11:104576557-104576905	GM12878	blood:	n/a	n/a
4	CBX3	chr11:104539778-104540232	HCT-116	colon:	n/a	n/a
5	CEBPB	chr11:104565857-104566073	HepG2	liver:	n/a	n/a
6	CEBPB	chr11:104525090-104525327	K562	blood:	n/a	chr11:104525181-104525194 chr11:104525181-104525194 chr11:104525181-104525194 chr11:104525181-104525192
7	CEBPB	chr11:104525013-104525262	A549	lung:	n/a	chr11:104525181-104525194 chr11:104525181-104525194 chr11:104525181-104525194 chr11:104525181-104525192
8	CEBPB	chr11:104539700-104540315	HCT-116	colon:	n/a	n/a
9	CEBPB	chr11:104571351-104571838	IMR90	lung:	n/a	n/a
10	CEBPB	chr11:104630751-104630812	HepG2	liver:	n/a	chr11:104630758-104630769
11	CEBPB	chr11:104525026-104525358	IMR90	lung:	n/a	chr11:104525322-104525333 chr11:104525181-104525194 chr11:104525181-104525194 chr11:104525181-104525194 chr11:104525181-104525192
12	CEBPB	chr11:104534113-104534393	IMR90	lung:	n/a	chr11:104534205-104534216
13	CEBPB	chr11:104539759-104540264	A549	lung:	n/a	n/a
14	CEBPB	chr11:104584302-104584553	HepG2	liver:	n/a	chr11:104584443-104584454
15	CEBPB	chr11:104565834-104566127	IMR90	lung:	n/a	n/a
16	CEBPB	chr11:104537084-104537209	H1-hESC	embryonic stem cell:	n/a	chr11:104537185-104537196
17	CEBPB	chr11:104539824-104540164	A549	lung:	n/a	n/a
18	CEBPB	chr11:104592226-104592334	HepG2	liver:	n/a	n/a
19	CEBPB	chr11:104539680-104540284	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr11:104550013-104550355	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr11:104536453-104536685	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr11:104536365-104536737	IMR90	lung:	n/a	n/a
23	CEBPB	chr11:104539817-104540111	HepG2	liver:	n/a	n/a
24	CEBPB	chr11:104601427-104601666	HepG2	liver:	n/a	chr11:104601561-104601570 chr11:104601559-104601572 chr11:104601560-104601571 chr11:104601597-104601608
25	CEBPB	chr11:104601432-104601743	IMR90	lung:	n/a	chr11:104601561-104601570 chr11:104601559-104601572 chr11:104601560-104601571 chr11:104601597-104601608
26	CEBPB	chr11:104539749-104540204	HCT-116	colon:	n/a	n/a
27	CEBPB	chr11:104563447-104563746	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr11:104596353-104596854	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr11:104571488-104571708	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr11:104539774-104540189	IMR90	lung:	n/a	n/a
31	CEBPB	chr11:104539838-104540124	A549	lung:	n/a	n/a
32	CEBPB	chr11:104537036-104537358	HepG2	liver:	n/a	chr11:104537185-104537196
33	CEBPB	chr11:104565388-104566175	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr11:104534104-104534298	HepG2	liver:	n/a	chr11:104534205-104534216
35	CREB1	chr11:104576585-104576883	GM12878	blood:	n/a	n/a
36	CTCF	chr11:104547895-104547994	GM20000	blood:	n/a	n/a
37	CTCF	chr11:104629380-104629530	GM12870	blood:	n/a	n/a
38	CTCF	chr11:104584370-104584376	GM10248	blood:	n/a	n/a
39	CTCF	chr11:104565020-104565170	BE2_C	brain:	n/a	chr11:104565124-104565133
40	CTCF	chr11:104609053-104609072	HUVEC	blood vessel:	n/a	n/a
41	CTCF	chr11:104629654-104629759	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr11:104628020-104628170	HCPEpiC	choroid plexus:	n/a	n/a
43	CTCF	chr11:104547879-104547973	Spleen_OC	spleen:	n/a	n/a
44	CTCF	chr11:104529974-104530048	Pancreas_OC	pancreas:	n/a	n/a
45	CTCF	chr11:104567727-104567800	Kidney_OC	kidney:	n/a	n/a
46	CTCF	chr11:104609048-104609077	GM12878	blood:	n/a	n/a
47	CTCF	chr11:104629695-104629723	GM12878	blood:	n/a	n/a
48	CTCF	chr11:104628020-104628170	HRPEpiC	eye:	n/a	n/a
49	CTCF	chr11:104627960-104628110	HRPEpiC	eye:	n/a	n/a
50	CTCF	chr11:104570380-104570530	HMF	breast:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:104621250-104621300	HIPEpiC	eye:	n/a
2	chr11:104621250-104621300	Hela-S3	cervix:	n/a
3	chr11:104576302-104576352	Caco-2	colon:	n/a
4	chr11:104576302-104576352	HRPEpiC	eye:	n/a
5	chr11:104621250-104621300	AoSMC	blood vessel:	n/a
6	chr11:104621250-104621300	BJ	skin:	n/a
7	chr11:104576302-104576352	NT2-D1	testis:	n/a
8	chr11:104621250-104621300	NB4	blood:	n/a
9	chr11:104621250-104621300	MCF-7	breast:	n/a
10	chr11:104576302-104576352	HNPCEpiC	eye:	n/a
11	chr11:104576302-104576352	SK-N-MC	brain:	n/a
12	chr11:104621250-104621300	AG09309	skin:	n/a
13	chr11:104621250-104621300	SKMC	muscle:	n/a
14	chr11:104621250-104621300	PrEC	prostate:	n/a
15	chr11:104621250-104621300	HRE	kidney:	n/a
16	chr11:104576302-104576352	BJ	skin:	n/a
17	chr11:104621250-104621300	GM12891	blood:	n/a
18	chr11:104576302-104576352	AG04449	skin:	fetal
19	chr11:104621250-104621300	GM12878	blood:	n/a
20	chr11:104576302-104576352	GM19239	blood:	n/a
21	chr11:104621250-104621300	U87	brain:	n/a
22	chr11:104621250-104621300	AG04449	skin:	fetal
23	chr11:104621250-104621300	Hepatocyte	liver:	n/a
24	chr11:104621250-104621300	HEEpiC	esophagus:	n/a
25	chr11:104621250-104621300	HRPEpiC	eye:	n/a
26	chr11:104621250-104621300	Jurkat	blood:	n/a
27	chr11:104621250-104621300	T-47D	breast:	n/a
28	chr11:104576302-104576352	HCPEpiC	choroid plexus:	n/a
29	chr11:104621250-104621300	ovcar-3	ovarian:	n/a
30	chr11:104576302-104576352	GM12892	blood:	n/a
31	chr11:104576302-104576352	AG10803	skin:	n/a
32	chr11:104576302-104576352	LNCaP	prostate:	n/a
33	chr11:104621250-104621300	RPTEC	kidney:	n/a
34	chr11:104576302-104576352	IMR90	lung:	fetal
35	chr11:104621250-104621300	HCPEpiC	choroid plexus:	n/a
36	chr11:104576302-104576352	HUVEC	blood vessel:	n/a
37	chr11:104621250-104621300	K562	blood:	n/a
38	chr11:104576302-104576352	ovcar-3	ovarian:	n/a
39	chr11:104621250-104621300	SAEC	small airway:	n/a
40	chr11:104576302-104576352	AG04450	lung:	fetal
41	chr11:104621250-104621300	NHDF-neo	bronchial:	n/a
42	chr11:104621250-104621300	A549	lung:	n/a
43	chr11:104621250-104621300	HL-60	blood:	n/a
44	chr11:104576302-104576352	Jurkat	blood:	n/a
45	chr11:104621250-104621300	AG10803	skin:	n/a
46	chr11:104621250-104621300	AG09319	gingival:	n/a
47	chr11:104621250-104621300	HUVEC	blood vessel:	n/a
48	chr11:104621250-104621300	GM19239	blood:	n/a
49	chr11:104621250-104621300	NT2-D1	testis:	n/a
50	chr11:104621250-104621300	SK-N-SH_RA	brain:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:104524242..104527061-chr11:104559725..104562588,2	K562	blood:
2	chr11:104625274..104625879-chr20:60553051..60553551,2	Hela-S3	cervix:
3	chr11:104598989..104600834-chr11:104611335..104614012,2	K562	blood:
4	chr11:104625193..104625713-chr4:116457976..116458496,2	MCF-7	breast:
5	chr11:104516723..104519201-chr11:104522234..104524667,2	K562	blood:
6	chr11:104598989..104600834-chr11:104611335..104614012,2	K562	blood:
7	chr11:104524242..104527061-chr11:104559725..104562588,2	K562	blood:

No data

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

Extended variants
information (count: 3207 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:3207 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17102811	chr11:104523335-104523336	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs150503083	chr11:104523479-104523480	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs528891969	chr11:104523481-104523482	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs557612419	chr11:104523519-104523520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs577544190	chr11:104523527-104523528	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs73625204	chr11:104523530-104523531	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs563538770	chr11:104523557-104523558	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs573758416	chr11:104523572-104523573	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs542680860	chr11:104523587-104523588	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs542195915	chr11:104523622-104523623	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs559505840	chr11:104523625-104523626	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs367725011	chr11:104523629-104523630	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs375761168	chr11:104523644-104523645	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs139654454	chr11:104523690-104523691	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs531298514	chr11:104523714-104523715	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs370478489	chr11:104523761-104523762	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs551564217	chr11:104523764-104523765	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs550218706	chr11:104523778-104523779	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs375432684	chr11:104523806-104523807	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs187870146	chr11:104523862-104523863	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs546444441	chr11:104523884-104523885	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs549028250	chr11:104523885-104523886	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs565867266	chr11:104523911-104523912	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs369358691	chr11:104523941-104523942	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs192714899	chr11:104524023-104524024	Flanking Active TSS Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs557776091	chr11:104524033-104524034	Flanking Active TSS Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs571440189	chr11:104524051-104524052	Flanking Active TSS Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs182375503	chr11:104524056-104524057	Flanking Active TSS Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs556998433	chr11:104524089-104524090	Flanking Active TSS Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs568230121	chr11:104524101-104524102	Flanking Active TSS Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs56320500	chr11:104524118-104524119	Flanking Active TSS Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs542878162	chr11:104524141-104524142	Flanking Active TSS Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs187821357	chr11:104524179-104524180	Flanking Active TSS Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs10895714	chr11:104524184-104524185	Flanking Active TSS Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs112668981	chr11:104524196-104524197	Flanking Active TSS Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs545015024	chr11:104524197-104524198	Flanking Active TSS Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs369451346	chr11:104524213-104524214	Flanking Active TSS Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs564829461	chr11:104524233-104524234	Flanking Active TSS Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs530428933	chr11:104524277-104524278	Flanking Active TSS Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs544064098	chr11:104524319-104524320	Flanking Active TSS Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs149322283	chr11:104524321-104524322	Flanking Active TSS Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs529471216	chr11:104524347-104524348	Flanking Active TSS Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs192680342	chr11:104524361-104524362	Flanking Active TSS Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs184833918	chr11:104524431-104524432	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs187156361	chr11:104524434-104524435	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs547338550	chr11:104524439-104524440	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs67225205	chr11:104524460-104524461	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs397848985	chr11:104524461-104524462	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs561699495	chr11:104524462-104524463	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs528604230	chr11:104524486-104524487	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

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
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:567 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:104520000-104523800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr11:104521400-104525400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr11:104523400-104525400	Enhancers	Dnd41	blood
4	chr11:104523800-104524000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr11:104523800-104524200	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
6	chr11:104523800-104524200	Active TSS	Aorta	Aorta
7	chr11:104523800-104524200	Active TSS	Brain Inferior Temporal Lobe	brain
8	chr11:104523800-104524200	Active TSS	Ovary	ovary
9	chr11:104523800-104524200	Active TSS	Right Atrium	heart
10	chr11:104523800-104524200	Enhancers	A549	lung
11	chr11:104523800-104524400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr11:104523800-104524400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
13	chr11:104523800-104524400	Active TSS	Rectal Mucosa Donor 29	rectum
14	chr11:104523800-104524600	Enhancers	Primary T helper naive cells from peripheral blood	blood
15	chr11:104523800-104524600	Enhancers	Fetal Heart	heart
16	chr11:104523800-104524800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
17	chr11:104524000-104524200	Active TSS	Brain Anterior Caudate	brain
18	chr11:104524000-104524400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr11:104524000-104524400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr11:104524000-104524400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
21	chr11:104524000-104524400	Enhancers	Adipose Nuclei	Adipose
22	chr11:104524000-104524400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
23	chr11:104524000-104524400	Active TSS	Colon Smooth Muscle	Colon
24	chr11:104524000-104524400	Enhancers	Fetal Kidney	kidney
25	chr11:104524000-104524600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
26	chr11:104524000-104524600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr11:104524000-104524600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr11:104524000-104524800	Enhancers	Primary hematopoietic stem cells short term culture	blood
29	chr11:104524000-104525400	Enhancers	Skeletal Muscle Female	skeletal muscle
30	chr11:104524000-104525600	Enhancers	Fetal Lung	lung
31	chr11:104524200-104524400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
32	chr11:104524200-104524400	Flanking Active TSS	Aorta	Aorta
33	chr11:104524200-104524400	Flanking Active TSS	Brain Anterior Caudate	brain
34	chr11:104524200-104524400	Flanking Active TSS	Ovary	ovary
35	chr11:104524200-104524400	Enhancers	Pancreas	Pancrea
36	chr11:104524200-104524400	Flanking Active TSS	Right Atrium	heart
37	chr11:104524200-104524400	Enhancers	Right Ventricle	heart
38	chr11:104524200-104524600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr11:104524200-104524600	Enhancers	Psoas Muscle	Psoas
40	chr11:104524200-104524600	Enhancers	Monocytes-CD14+_RO01746	blood
41	chr11:104524200-104524600	Enhancers	NHLF	lung
42	chr11:104524200-104524800	Enhancers	Skeletal Muscle Male	skeletal muscle
43	chr11:104524200-104527600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
44	chr11:104524400-104525400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr11:104524800-104525200	Weak transcription	Skeletal Muscle Male	skeletal muscle
46	chr11:104525200-104525400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
47	chr11:104525200-104525600	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr11:104525400-104525600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr11:104525400-104525600	Enhancers	Skeletal Muscle Male	skeletal muscle
50	chr11:104527600-104528400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood

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