Variant report

Variant	esv1845235
Chromosome Location	chr11:34357429-34363950
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:118)
CpG islands
(count:61)
Chromatin interactive
region (count:8)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:118 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:34360799-34361380	HepG2	liver:	n/a	n/a
2	BCL11A	chr11:34360766-34361087	GM12878	blood:	n/a	n/a
3	BCL3	chr11:34360702-34361332	A549	lung:	n/a	n/a
4	BCL3	chr11:34360618-34361152	A549	lung:	n/a	n/a
5	BHLHE40	chr11:34360785-34361082	GM12878	blood:	n/a	n/a
6	CEBPB	chr11:34360879-34361234	HepG2	liver:	n/a	n/a
7	CEBPB	chr11:34360816-34361282	HepG2	liver:	n/a	n/a
8	CEBPB	chr11:34360778-34361291	HepG2	liver:	n/a	n/a
9	CEBPB	chr11:34360863-34361379	A549	lung:	n/a	n/a
10	CEBPB	chr11:34360755-34361214	A549	lung:	n/a	n/a
11	CEBPB	chr11:34360601-34361582	A549	lung:	n/a	chr11:34361370-34361383
12	CEBPB	chr11:34360798-34361445	HepG2	liver:	n/a	chr11:34361370-34361383
13	CEBPD	chr11:34360773-34361106	HepG2	liver:	n/a	n/a
14	CEBPD	chr11:34360862-34361160	HepG2	liver:	n/a	n/a
15	CHD2	chr11:34360952-34360995	GM12878	blood:	n/a	n/a
16	CTCF	chr11:34363760-34363910	AoAF	blood vessel:	n/a	n/a
17	CTCF	chr11:34363780-34363930	AoAF	blood vessel:	n/a	n/a
18	CTCF	chr11:34363800-34363950	HRPEpiC	eye:	n/a	n/a
19	CTCF	chr11:34363760-34363910	HCPEpiC	choroid plexus:	n/a	n/a
20	CTCF	chr11:34363780-34363930	HCPEpiC	choroid plexus:	n/a	n/a
21	CTCF	chr11:34363800-34363950	GM12864	blood:	n/a	n/a
22	CTCF	chr11:34363815-34363893	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr11:34363840-34363990	HAc	cerebellar:	n/a	n/a
24	CTCF	chr11:34363740-34363890	BJ	skin:	n/a	n/a
25	EBF1	chr11:34360839-34361077	GM12878	blood:	n/a	n/a
26	ELF1	chr11:34360927-34361262	HepG2	liver:	n/a	n/a
27	ELF1	chr11:34360887-34361346	HepG2	liver:	n/a	n/a
28	EP300	chr11:34360800-34361319	HepG2	liver:	n/a	n/a
29	EP300	chr11:34360662-34361348	HepG2	liver:	n/a	n/a
30	EP300	chr11:34360785-34361168	GM12878	blood:	n/a	n/a
31	EP300	chr11:34360754-34361107	GM12878	blood:	n/a	n/a
32	EP300	chr11:34360619-34361380	A549	lung:	n/a	n/a
33	EP300	chr11:34360538-34361637	A549	lung:	n/a	n/a
34	FOS	chr11:34361231-34361337	MCF10A-Er-Src	breast:	n/a	n/a
35	FOSL2	chr11:34360681-34361494	A549	lung:	n/a	n/a
36	FOXA1	chr11:34360720-34361397	HepG2	liver:	n/a	chr11:34360969-34360981
37	FOXA1	chr11:34363392-34363784	T-47D	breast:	n/a	n/a
38	FOXA1	chr11:34363352-34363798	T-47D	breast:	n/a	n/a
39	FOXA1	chr11:34360714-34361397	HepG2	liver:	n/a	chr11:34360969-34360981
40	FOXA1	chr11:34360777-34361310	HepG2	liver:	n/a	chr11:34360969-34360981
41	FOXA1	chr11:34360696-34361227	HepG2	liver:	n/a	chr11:34360969-34360981
42	FOXA2	chr11:34360670-34361238	A549	lung:	n/a	chr11:34360969-34360981
43	FOXA2	chr11:34363425-34363885	A549	lung:	n/a	n/a
44	FOXA2	chr11:34362221-34362714	A549	lung:	n/a	chr11:34362409-34362421
45	FOXA2	chr11:34360788-34361497	HepG2	liver:	n/a	chr11:34360969-34360981
46	FOXA2	chr11:34360701-34361613	A549	lung:	n/a	chr11:34360969-34360981
47	GATA3	chr11:34357851-34358199	T-47D	breast:	n/a	n/a
48	GATA3	chr11:34360701-34361436	A549	lung:	n/a	chr11:34361148-34361159 chr11:34360965-34360974
49	GATA3	chr11:34357761-34358279	T-47D	breast:	n/a	n/a
50	GATA3	chr11:34357889-34358174	MCF-7	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:34363786-34363836	NHBE	bronchial:	n/a
2	chr11:34363786-34363836	HCPEpiC	choroid plexus:	n/a
3	chr11:34363786-34363836	AG10803	skin:	n/a
4	chr11:34363786-34363836	Caco-2	colon:	n/a
5	chr11:34363786-34363836	GM12891	blood:	n/a
6	chr11:34363786-34363836	Hepatocyte	liver:	n/a
7	chr11:34363786-34363836	AG09319	gingival:	n/a
8	chr11:34363786-34363836	PrEC	prostate:	n/a
9	chr11:34363786-34363836	HIPEpiC	eye:	n/a
10	chr11:34363786-34363836	BJ	skin:	n/a
11	chr11:34363786-34363836	HCF	heart:	n/a
12	chr11:34363786-34363836	SK-N-SH	brain:	n/a
13	chr11:34363786-34363836	NT2-D1	testis:	n/a
14	chr11:34363786-34363836	NB4	blood:	n/a
15	chr11:34363786-34363836	A549	lung:	n/a
16	chr11:34363786-34363836	HRPEpiC	eye:	n/a
17	chr11:34363786-34363836	LNCaP	prostate:	n/a
18	chr11:34363786-34363836	GM12878	blood:	n/a
19	chr11:34363786-34363836	AG04449	skin:	fetal
20	chr11:34363786-34363836	HNPCEpiC	eye:	n/a
21	chr11:34363786-34363836	AG04450	lung:	fetal
22	chr11:34363786-34363836	BE2_C	brain:	n/a
23	chr11:34363786-34363836	HRCEpiC	kidney:	n/a
24	chr11:34363786-34363836	RPTEC	kidney:	n/a
25	chr11:34363786-34363836	HEEpiC	esophagus:	n/a
26	chr11:34363786-34363836	IMR90	lung:	fetal
27	chr11:34363786-34363836	MCF-7	breast:	n/a
28	chr11:34363786-34363836	PFSK-1	brain:	n/a
29	chr11:34363786-34363836	AG09309	skin:	n/a
30	chr11:34363786-34363836	PANC-1	pancreas:	n/a
31	chr11:34363786-34363836	HRE	kidney:	n/a
32	chr11:34363786-34363836	SAEC	small airway:	n/a
33	chr11:34363786-34363836	ovcar-3	ovarian:	n/a
34	chr11:34363786-34363836	HepG2	liver:	n/a
35	chr11:34363786-34363836	GM19239	blood:	n/a
36	chr11:34363786-34363836	HL-60	blood:	n/a
37	chr11:34363786-34363836	Jurkat	blood:	n/a
38	chr11:34363786-34363836	CMK	blood:	n/a
39	chr11:34363786-34363836	HEK293	kidney:	embryo
40	chr11:34363786-34363836	SKMC	muscle:	n/a
41	chr11:34363786-34363836	SK-N-MC	brain:	n/a
42	chr11:34363786-34363836	Hela-S3	cervix:	n/a
43	chr11:34363786-34363836	HUVEC	blood vessel:	n/a
44	chr11:34363786-34363836	H1-hESC	embryonic stem cell:	embryo
45	chr11:34363786-34363836	GM06990	blood:	n/a
46	chr11:34363786-34363836	U87	brain:	n/a
47	chr11:34363786-34363836	HAEpiC	amniotic membrane:	n/a
48	chr11:34363786-34363836	GM12892	blood:	n/a
49	chr11:34363786-34363836	SK-N-SH_RA	brain:	n/a
50	chr11:34363786-34363836	NHDF-neo	bronchial:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:34359062..34360575-chr11:34363505..34365400,2	K562	blood:
2	chr11:34357216..34358836-chr11:34360327..34362099,2	K562	blood:
3	chr11:34363297..34366211-chr11:34370921..34372477,2	K562	blood:
4	chr11:34283475..34285529-chr11:34358260..34360841,2	MCF-7	breast:
5	chr11:34065587..34067431-chr11:34358883..34361873,2	K562	blood:
6	chr11:34359062..34360575-chr11:34363505..34365400,2	K562	blood:
7	chr11:34355811..34357452-chr2:150425166..150428140,2	MCF-7	breast:
8	chr11:34360672..34363341-chr11:34364599..34366363,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ELF5-4	chr11:34356665-34357550	NONHSAT018749

No data

Variant related genes	Relation type
ENSG00000254708	TF binding region
ENSG00000254708	CpG island
ENSG00000254708	chromatin interactions

Extended variants
information (count: 270 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:270 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs186036114	chr11:34357451-34357452	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
2	rs375393691	chr11:34357452-34357453	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
3	rs562564117	chr11:34357506-34357507	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
4	rs367969693	chr11:34357509-34357510	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
5	rs11545271	chr11:34357541-34357542	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
6	rs11545268	chr11:34357544-34357545	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
7	rs11545267	chr11:34357549-34357550	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
8	rs529795720	chr11:34357563-34357564	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs551029984	chr11:34357578-34357579	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs570901074	chr11:34357641-34357642	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs141475713	chr11:34357672-34357673	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs557196774	chr11:34357712-34357713	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs551912412	chr11:34357748-34357749	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs565541436	chr11:34357775-34357776	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs532878886	chr11:34357800-34357801	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs534577242	chr11:34357829-34357830	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs78902453	chr11:34357846-34357847	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs142056317	chr11:34357864-34357865	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs536695196	chr11:34357888-34357889	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs188490224	chr11:34357903-34357904	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs576825458	chr11:34357928-34357929	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs549574483	chr11:34357968-34357969	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs151132648	chr11:34357974-34357975	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs140097972	chr11:34357999-34358000	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs150316627	chr11:34358030-34358031	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs562270198	chr11:34358031-34358032	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs370573512	chr11:34358035-34358036	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs544318921	chr11:34358044-34358045	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs74935873	chr11:34358049-34358050	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs533205685	chr11:34358062-34358063	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs181520977	chr11:34358093-34358094	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs565523157	chr11:34358144-34358145	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs528299621	chr11:34358147-34358148	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs547285748	chr11:34358189-34358190	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs548463219	chr11:34358194-34358195	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs568305976	chr11:34358199-34358200	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs540963021	chr11:34358215-34358216	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs11607456	chr11:34358247-34358248	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs559199317	chr11:34358249-34358250	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs186463885	chr11:34358258-34358259	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs60514474	chr11:34358282-34358283	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs7944461	chr11:34358300-34358301	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs575691049	chr11:34358301-34358302	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs542103777	chr11:34358314-34358315	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs556015240	chr11:34358323-34358324	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs190902714	chr11:34358397-34358398	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs16925440	chr11:34358408-34358409	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs71457335	chr11:34358444-34358445	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs7929828	chr11:34358476-34358477	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs533171527	chr11:34358531-34358532	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Medulloblastoma	16783165	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18194544	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	21364760	CNVD
Aniridia syndrome	21572526	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Retinoblastoma	22278416	CNVD
Denys-drash syndrome	21085971	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
WAGR syndrome	16773131	CNVD
Disorders of sex development	22290220	CNVD
Aniridia syndrome	17204608	CNVD
Mental retardation	17204608	CNVD
WAGR syndrome	19617690	CNVD
genitourinary abnormalities	17204608	CNVD
Breast cancer	16397240	CNVD
Mental retardation	16773131	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Cancer	21183584	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
WAGR syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Denys-drash syndrome	19566914	CNVD
Familial wilms tumor	19566914	CNVD
Frasier syndrome	19566914	CNVD
Non-small cell lung cancer	21829676	CNVD
WAGR syndrome	20603712	CNVD
Autism	17322880	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21858162	CNVD
Cancer	20164920	CNVD
Breast cancer	16620391	CNVD

Chromatin state (count:203 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:34336200-34358200	Weak transcription	Thymus	Thymus
2	chr11:34351800-34363800	Weak transcription	Left Ventricle	heart
3	chr11:34352600-34363800	Weak transcription	Gastric	stomach
4	chr11:34352800-34358600	Enhancers	HepG2	liver
5	chr11:34353200-34360800	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr11:34353200-34365400	Weak transcription	Pancreas	Pancrea
7	chr11:34353400-34362800	Weak transcription	Right Atrium	heart
8	chr11:34353800-34360800	Weak transcription	HSMMtube	muscle
9	chr11:34354000-34358600	Weak transcription	Skeletal Muscle Female	skeletal muscle
10	chr11:34354000-34360800	Weak transcription	HSMM	muscle
11	chr11:34354400-34360800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr11:34354400-34362200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr11:34354400-34363800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr11:34354400-34366600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr11:34354600-34358600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr11:34354600-34358600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr11:34354600-34362600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr11:34354600-34363000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
19	chr11:34354600-34363800	Weak transcription	NH-A	brain
20	chr11:34354800-34363000	Weak transcription	HUES6 Cell Line	embryonic stem cell
21	chr11:34355600-34358600	Weak transcription	Primary B cells from cord blood	blood
22	chr11:34355600-34360600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr11:34355800-34358600	Weak transcription	Primary hematopoietic stem cells	blood
24	chr11:34355800-34359400	Weak transcription	Primary monocytes fromperipheralblood	blood
25	chr11:34355800-34360400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr11:34356000-34358200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
27	chr11:34356000-34358400	Weak transcription	Primary neutrophils fromperipheralblood	blood
28	chr11:34356200-34361800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
29	chr11:34356400-34360800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr11:34357000-34360600	Enhancers	A549	lung
31	chr11:34357200-34357600	Enhancers	Liver	Liver
32	chr11:34357400-34357600	Enhancers	GM12878-XiMat	blood
33	chr11:34357400-34358000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr11:34357400-34360000	Enhancers	Fetal Thymus	thymus
35	chr11:34357600-34360200	Weak transcription	Liver	Liver
36	chr11:34357600-34360400	Weak transcription	GM12878-XiMat	blood
37	chr11:34358000-34361000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr11:34358200-34359400	Enhancers	Thymus	Thymus
39	chr11:34358200-34362000	Enhancers	Primary hematopoietic stem cells short term culture	blood
40	chr11:34358400-34359600	Enhancers	Primary T cells from cord blood	blood
41	chr11:34358400-34360600	Enhancers	Primary neutrophils fromperipheralblood	blood
42	chr11:34358600-34359000	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr11:34358600-34359000	Enhancers	Skeletal Muscle Female	skeletal muscle
44	chr11:34358600-34359200	Enhancers	Primary B cells from cord blood	blood
45	chr11:34358600-34359400	Enhancers	Primary hematopoietic stem cells	blood
46	chr11:34358600-34359600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
47	chr11:34358600-34359800	Genic enhancers	HepG2	liver
48	chr11:34358800-34359000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr11:34359000-34360400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr11:34359000-34361000	Weak transcription	Skeletal Muscle Female	skeletal muscle

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