Variant report

Variant	esv3471041
Chromosome Location	chr11:71212614-71215837
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:27)
CpG islands
(count:61)
Chromatin interactive
region (count:6)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:27 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr11:71215809-71215924	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr11:71215097-71215297	HepG2	liver:	n/a	n/a
3	EP300	chr11:71215429-71216087	ECC-1	luminal epithelium:	n/a	n/a
4	HDAC2	chr11:71215431-71215945	MCF-7	breast:	n/a	n/a
5	IRF3	chr11:71215206-71215312	GM12878	blood:	n/a	n/a
6	MAX	chr11:71215442-71215998	MCF-7	breast:	n/a	n/a
7	MAX	chr11:71212379-71212843	ECC-1	luminal epithelium:	n/a	n/a
8	MAX	chr11:71215510-71215915	ECC-1	luminal epithelium:	n/a	n/a
9	MAX	chr11:71212358-71212813	ECC-1	luminal epithelium:	n/a	n/a
10	MAX	chr11:71215427-71215976	MCF-7	breast:	n/a	n/a
11	MYC	chr11:71215669-71215781	MCF-7	breast:	n/a	n/a
12	MYC	chr11:71215680-71215747	MCF-7	breast:	n/a	n/a
13	MYC	chr11:71214744-71214820	GM12878	blood:	n/a	n/a
14	NFIC	chr11:71212438-71212789	ECC-1	luminal epithelium:	n/a	n/a
15	NFIC	chr11:71215456-71216054	ECC-1	luminal epithelium:	n/a	n/a
16	NFIC	chr11:71215427-71216220	ECC-1	luminal epithelium:	n/a	n/a
17	POLR2A	chr11:71214773-71214854	ProgFib	skin:	n/a	n/a
18	POLR2A	chr11:71214745-71214751	ProgFib	skin:	n/a	n/a
19	POLR2A	chr11:71214069-71214147	HUVEC	blood vessel:	n/a	n/a
20	SIN3A	chr11:71215809-71215957	H1-hESC	embryonic stem cell:	n/a	n/a
21	SIN3AK20	chr11:71215520-71216080	MCF-7	breast:	n/a	n/a
22	TCF12	chr11:71215515-71215984	ECC-1	luminal epithelium:	n/a	n/a
23	TCF12	chr11:71215423-71216060	ECC-1	luminal epithelium:	n/a	n/a
24	TEAD4	chr11:71215532-71215961	ECC-1	luminal epithelium:	n/a	n/a
25	YY1	chr11:71215587-71215910	ECC-1	luminal epithelium:	n/a	n/a
26	YY1	chr11:71215545-71215934	ECC-1	luminal epithelium:	n/a	n/a
27	ZNF217	chr11:71215589-71215942	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	chr11:71215361-71215411	MCF-7	breast:	n/a
2	chr11:71215361-71215411	HRE	kidney:	n/a
3	chr11:71215361-71215411	H1-hESC	embryonic stem cell:	embryo
4	chr11:71215361-71215411	NHDF-neo	bronchial:	n/a
5	chr11:71215361-71215411	AG09309	skin:	n/a
6	chr11:71215361-71215411	A549	lung:	n/a
7	chr11:71215361-71215411	HAEpiC	amniotic membrane:	n/a
8	chr11:71215361-71215411	SK-N-MC	brain:	n/a
9	chr11:71215361-71215411	MCF10A-Er-Src	breast:	n/a
10	chr11:71215361-71215411	Caco-2	colon:	n/a
11	chr11:71215361-71215411	AG10803	skin:	n/a
12	chr11:71215361-71215411	HNPCEpiC	eye:	n/a
13	chr11:71215361-71215411	Hepatocyte	liver:	n/a
14	chr11:71215361-71215411	BJ	skin:	n/a
15	chr11:71215361-71215411	ECC-1	luminal epithelium:	n/a
16	chr11:71215361-71215411	HCM	heart:	n/a
17	chr11:71215361-71215411	GM12892	blood:	n/a
18	chr11:71215361-71215411	NT2-D1	testis:	n/a
19	chr11:71215361-71215411	HepG2	liver:	n/a
20	chr11:71215361-71215411	NH-A	brain:	n/a
21	chr11:71215361-71215411	RPTEC	kidney:	n/a
22	chr11:71215361-71215411	GM19239	blood:	n/a
23	chr11:71215361-71215411	Hela-S3	cervix:	n/a
24	chr11:71215361-71215411	HEK293	kidney:	embryo
25	chr11:71215361-71215411	PANC-1	pancreas:	n/a
26	chr11:71215361-71215411	NB4	blood:	n/a
27	chr11:71215361-71215411	SKMC	muscle:	n/a
28	chr11:71215361-71215411	SAEC	small airway:	n/a
29	chr11:71215361-71215411	HPAEpiC	pulmonary alveolar:	n/a
30	chr11:71215361-71215411	HMEC	breast:	n/a
31	chr11:71215361-71215411	Jurkat	blood:	n/a
32	chr11:71215361-71215411	AG04449	skin:	fetal
33	chr11:71215361-71215411	BE2_C	brain:	n/a
34	chr11:71215361-71215411	HCPEpiC	choroid plexus:	n/a
35	chr11:71215361-71215411	GM12891	blood:	n/a
36	chr11:71215361-71215411	ProgFib	skin:	n/a
37	chr11:71215361-71215411	LNCaP	prostate:	n/a
38	chr11:71215361-71215411	ovcar-3	ovarian:	n/a
39	chr11:71215361-71215411	NHBE	bronchial:	n/a
40	chr11:71215361-71215411	HCT-116	colon:	n/a
41	chr11:71215361-71215411	K562	blood:	n/a
42	chr11:71215361-71215411	PrEC	prostate:	n/a
43	chr11:71215361-71215411	SK-N-SH_RA	brain:	n/a
44	chr11:71215361-71215411	PFSK-1	brain:	n/a
45	chr11:71215361-71215411	HIPEpiC	eye:	n/a
46	chr11:71215361-71215411	IMR90	lung:	fetal
47	chr11:71215361-71215411	AoSMC	blood vessel:	n/a
48	chr11:71215361-71215411	HCF	heart:	n/a
49	chr11:71215361-71215411	SK-N-SH	brain:	n/a
50	chr11:71215361-71215411	HRCEpiC	kidney:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:71209374..71211618-chr11:71213015..71214853,2	K562	blood:
2	chr11:71210029..71213708-chr11:71213873..71217585,6	MCF-7	breast:
3	chr11:71214959..71216939-chr11:71218643..71221307,2	K562	blood:
4	chr11:71212078..71213595-chr11:71215421..71217314,2	K562	blood:
5	chr11:71212078..71213595-chr11:71215421..71217314,2	K562	blood:
6	chr11:71205951..71209347-chr11:71211780..71215363,4	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KRTAP5-7-1	chr11:71214910-71216920	NONHSAT022690
2	lnc-KRTAP5-7-1	chr11:71214591-71214787	NONHSAT022689
3	lnc-KRTAP5-7-1	chr11:71215112-71215524	NONHSAT022689

No data

Variant related genes	Relation type
NADSYN1	TF binding region
NADSYN1	CpG island
ENSG00000254924	chromatin interactions
ENSG00000172890	chromatin interactions

Extended variants
information (count: 165 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:165 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs548369523	chr11:71212626-71212627	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs560063119	chr11:71212631-71212632	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs113263840	chr11:71212638-71212639	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs528615148	chr11:71212641-71212642	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs547103429	chr11:71212657-71212658	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs181766110	chr11:71212658-71212659	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs186136512	chr11:71212698-71212699	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs551338602	chr11:71212725-71212726	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs116182788	chr11:71212882-71212883	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs536515838	chr11:71212883-71212884	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs143316631	chr11:71212900-71212901	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs60600601	chr11:71212923-71212924	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs11233947	chr11:71212924-71212925	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs558224147	chr11:71212949-71212950	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs116747072	chr11:71212976-71212977	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs751389	chr11:71213007-71213008	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs79518585	chr11:71213020-71213021	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs372137831	chr11:71213030-71213031	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs541727701	chr11:71213035-71213036	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs560332798	chr11:71213039-71213040	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs190992929	chr11:71213058-71213059	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs527460918	chr11:71213074-71213075	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs547162836	chr11:71213081-71213082	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs545984759	chr11:71213088-71213089	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs147544124	chr11:71213132-71213133	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs558194327	chr11:71213167-71213168	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs532612109	chr11:71213184-71213185	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs117965011	chr11:71213199-71213200	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs569121962	chr11:71213207-71213208	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs536986918	chr11:71213208-71213209	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs548579194	chr11:71213243-71213244	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs566768418	chr11:71213287-71213288	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs180777397	chr11:71213299-71213300	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs113468949	chr11:71213321-71213322	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs558683910	chr11:71213372-71213373	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs11233950	chr11:71213373-71213374	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs537521444	chr11:71213383-71213384	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs556142489	chr11:71213389-71213390	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs185238305	chr11:71213412-71213413	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs369946613	chr11:71213444-71213445	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs4945001	chr11:71213465-71213466	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs111819453	chr11:71213488-71213489	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs34889297	chr11:71213499-71213500	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs553779505	chr11:71213528-71213529	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs34678969	chr11:71213535-71213536	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs34279018	chr11:71213540-71213541	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs7939135	chr11:71213552-71213553	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs34689169	chr11:71213561-71213562	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs34274142	chr11:71213619-71213620	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs369144421	chr11:71213631-71213632	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20067559	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
Lung cancer	18438408	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Glioblastoma multiforme	21080181	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chordoma	21602918	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Multiple myeloma	16616336	CNVD
Urothelial cell carcinoma	18451213	CNVD
Leukoplakia	24403051	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	19812545	CNVD

Chromatin state (count:237 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:71165800-71218400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
2	chr11:71181400-71217800	Strong transcription	Primary monocytes fromperipheralblood	blood
3	chr11:71181800-71218000	Strong transcription	Monocytes-CD14+_RO01746	blood
4	chr11:71182000-71217600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr11:71182200-71216000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr11:71182200-71216200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr11:71182200-71216200	Strong transcription	Rectal Mucosa Donor 31	rectum
8	chr11:71182200-71217800	Strong transcription	Primary T cells from cord blood	blood
9	chr11:71182400-71213800	Strong transcription	Rectal Mucosa Donor 29	rectum
10	chr11:71182400-71217200	Strong transcription	Sigmoid Colon	Sigmoid Colon
11	chr11:71182400-71217600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr11:71182400-71217800	Strong transcription	Duodenum Mucosa	Duodenum
13	chr11:71182600-71213600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr11:71182800-71216400	Strong transcription	Stomach Smooth Muscle	stomach
15	chr11:71183000-71213400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr11:71189800-71218400	Strong transcription	Primary neutrophils fromperipheralblood	blood
17	chr11:71199400-71214600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr11:71199400-71215600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
19	chr11:71199600-71213000	Strong transcription	Primary B cells from cord blood	blood
20	chr11:71199600-71216400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr11:71199600-71218400	Strong transcription	Fetal Intestine Small	intestine
22	chr11:71200000-71215000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr11:71200000-71216000	Strong transcription	Primary T helper cells fromperipheralblood	blood
24	chr11:71200200-71213200	Strong transcription	Primary T cells fromperipheralblood	blood
25	chr11:71200200-71216000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
26	chr11:71200200-71216400	Strong transcription	Primary B cells from peripheral blood	blood
27	chr11:71200200-71217400	Strong transcription	Fetal Intestine Large	intestine
28	chr11:71200400-71213200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr11:71200400-71213800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr11:71200400-71216200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
31	chr11:71200400-71216400	Strong transcription	Primary T helper cells PMA-I stimulated	--
32	chr11:71200600-71213200	Strong transcription	HUES6 Cell Line	embryonic stem cell
33	chr11:71200800-71215400	Strong transcription	Placenta	Placenta
34	chr11:71200800-71216800	Weak transcription	Fetal Kidney	kidney
35	chr11:71201000-71214600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr11:71201000-71215200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr11:71201000-71216200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr11:71201200-71213000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr11:71201200-71215400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr11:71201800-71216400	Strong transcription	Ovary	ovary
41	chr11:71203200-71215200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr11:71203400-71216800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr11:71205000-71213200	Strong transcription	Brain Angular Gyrus	brain
44	chr11:71205000-71214600	Strong transcription	Esophagus	oesophagus
45	chr11:71205200-71213000	Strong transcription	Brain Anterior Caudate	brain
46	chr11:71205200-71213000	Strong transcription	Rectal Smooth Muscle	rectum
47	chr11:71205200-71213400	Strong transcription	HepG2	liver
48	chr11:71205200-71215600	Strong transcription	Colonic Mucosa	Colon
49	chr11:71205200-71215600	Strong transcription	Duodenum Smooth Muscle	Duodenum
50	chr11:71205200-71216000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--

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