Variant report

Variant	nsv819658
Chromosome Location	chr11:65757756-65764902
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:66)
CpG islands
(count:0)
Chromatin interactive
region (count:42)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:66 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr11:65764854-65764996	K562	blood:	n/a	n/a
2	CEBPB	chr11:65764858-65765080	K562	blood:	n/a	n/a
3	CEBPB	chr11:65763162-65763352	HepG2	liver:	n/a	chr11:65763234-65763245
4	CEBPB	chr11:65763070-65763322	MCF-7	breast:	n/a	chr11:65763234-65763245
5	CEBPB	chr11:65763232-65763274	H1-hESC	embryonic stem cell:	n/a	chr11:65763234-65763245
6	CEBPB	chr11:65763149-65763297	IMR90	lung:	n/a	chr11:65763234-65763245
7	CEBPB	chr11:65763126-65763326	A549	lung:	n/a	chr11:65763234-65763245
8	CEBPB	chr11:65763120-65763263	K562	blood:	n/a	chr11:65763234-65763245
9	CEBPB	chr11:65764779-65765122	K562	blood:	n/a	n/a
10	CTCF	chr11:65762660-65762810	RPTEC	kidney:	n/a	n/a
11	CTCF	chr11:65764860-65765010	AG04449	skin:	n/a	n/a
12	CTCF	chr11:65764840-65764990	HCPEpiC	choroid plexus:	n/a	n/a
13	CTCF	chr11:65764800-65764950	HBMEC	blood vessel:	n/a	n/a
14	CTCF	chr11:65764864-65765051	K562	blood:	n/a	n/a
15	CTCF	chr11:65764900-65765050	HEK293	kidney:	n/a	n/a
16	CTCF	chr11:65764900-65765050	HPAF	blood vessel:	n/a	n/a
17	CTCF	chr11:65764820-65764970	BE2_C	brain:	n/a	n/a
18	CTCF	chr11:65764880-65765030	HAc	cerebellar:	n/a	n/a
19	EP300	chr11:65762717-65762725	K562	blood:	n/a	n/a
20	MAX	chr11:65764817-65765037	K562	blood:	n/a	n/a
21	POLR2A	chr11:65764762-65765199	K562	blood:	n/a	n/a
22	POLR2A	chr11:65762448-65763050	K562	blood:	n/a	n/a
23	POLR2A	chr11:65761262-65761290	MCF-7	breast:	n/a	n/a
24	POLR2A	chr11:65764828-65765086	HL-60	blood:	n/a	n/a
25	POLR2A	chr11:65763554-65763578	HepG2	liver:	n/a	n/a
26	POLR2A	chr11:65762551-65762572	Hela-S3	cervix:	n/a	n/a
27	POLR2A	chr11:65764807-65765233	HepG2	liver:	n/a	n/a
28	POLR2A	chr11:65764712-65765310	K562	blood:	n/a	n/a
29	POLR2A	chr11:65762608-65762841	HepG2	liver:	n/a	n/a
30	POLR2A	chr11:65763570-65763711	H1-hESC	embryonic stem cell:	n/a	n/a
31	POLR2A	chr11:65764097-65764276	K562	blood:	n/a	n/a
32	POLR2A	chr11:65763149-65763461	K562	blood:	n/a	n/a
33	POLR2A	chr11:65759782-65759820	K562	blood:	n/a	n/a
34	POLR2A	chr11:65759756-65759770	K562	blood:	n/a	n/a
35	POLR2A	chr11:65764059-65764515	PANC-1	pancreas:	n/a	n/a
36	POLR2A	chr11:65764275-65764647	K562	blood:	n/a	n/a
37	POLR2A	chr11:65762719-65762720	ProgFib	skin:	n/a	n/a
38	POLR2A	chr11:65764804-65765219	K562	blood:	n/a	n/a
39	POLR2A	chr11:65764786-65765741	GM12878	blood:	n/a	n/a
40	POLR2A	chr11:65759730-65759948	HepG2	liver:	n/a	n/a
41	POLR2A	chr11:65764707-65765231	HL-60	blood:	n/a	n/a
42	POLR2A	chr11:65764544-65764630	GM12878	blood:	n/a	n/a
43	POLR2A	chr11:65762977-65763449	HepG2	liver:	n/a	n/a
44	POLR2A	chr11:65761300-65761319	MCF-7	breast:	n/a	n/a
45	POLR2A	chr11:65764753-65765214	GM12878	blood:	n/a	n/a
46	POLR2A	chr11:65762782-65763362	PFSK-1	brain:	n/a	n/a
47	POLR2A	chr11:65764191-65764929	HepG2	liver:	n/a	n/a
48	POLR2A	chr11:65764196-65764576	K562	blood:	n/a	n/a
49	POLR2A	chr11:65764734-65765351	SK-N-MC	brain:	n/a	n/a
50	POLR2A	chr11:65764697-65765336	PFSK-1	brain:	n/a	n/a

No data

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:65755347..65758083-chr11:65763733..65766415,2	K562	blood:
2	chr11:65758864..65760871-chr11:65762649..65765214,2	MCF-7	breast:
3	chr11:65759662..65761884-chr11:65763291..65764975,2	MCF-7	breast:
4	chr11:65754920..65762066-chr11:65768032..65772490,9	K562	blood:
5	chr11:65755347..65758083-chr11:65763733..65766415,2	K562	blood:
6	chr11:65748017..65751656-chr11:65762573..65766422,5	K562	blood:
7	chr11:65759662..65761884-chr11:65763291..65764975,2	MCF-7	breast:
8	chr11:65478250..65480362-chr11:65755788..65758079,2	K562	blood:
9	chr11:65764048..65767930-chr11:65768133..65771443,5	MCF-7	breast:
10	chr11:65743310..65746046-chr11:65763797..65766517,3	MCF-7	breast:
11	chr11:65726801..65730087-chr11:65756890..65758859,3	MCF-7	breast:
12	chr11:65752788..65755729-chr11:65758294..65759811,2	K562	blood:
13	chr11:65755935..65759042-chr11:65762460..65765703,3	MCF-7	breast:
14	chr11:65756748..65758854-chr11:65817829..65819589,2	MCF-7	breast:
15	chr11:65762816..65765321-chr11:65799547..65802531,2	MCF-7	breast:
16	chr11:65756651..65758382-chr11:65762755..65764832,2	MCF-7	breast:
17	chr11:65756651..65758382-chr11:65762755..65764832,2	MCF-7	breast:
18	chr11:65479793..65481375-chr11:65755148..65758058,2	MCF-7	breast:
19	chr11:65764589..65766874-chr11:65774811..65776588,2	K562	blood:
20	chr11:65743772..65746115-chr11:65755090..65757829,2	K562	blood:
21	chr11:65749300..65751914-chr11:65760648..65762675,2	K562	blood:
22	chr11:65656283..65659503-chr11:65753735..65758197,4	MCF-7	breast:
23	chr11:65755441..65758001-chr11:65788479..65791196,3	MCF-7	breast:
24	chr11:65478565..65481119-chr11:65754473..65758091,4	MCF-7	breast:
25	chr11:65756379..65757093-chr11:65764476..65765013,2	K562	blood:
26	chr11:65656308..65659356-chr11:65753544..65758296,4	MCF-7	breast:
27	chr11:65755754..65758071-chr11:65759625..65762366,2	K562	blood:
28	chr11:65684400..65687504-chr11:65755771..65760818,5	MCF-7	breast:
29	chr11:65758856..65761840-chr11:65835793..65837474,2	MCF-7	breast:
30	chr11:65758864..65760871-chr11:65762649..65765214,2	MCF-7	breast:
31	chr11:65762506..65765263-chr11:67235744..67237366,2	MCF-7	breast:
32	chr11:65654372..65655973-chr11:65756609..65758755,2	MCF-7	breast:
33	chr11:65755952..65758333-chr11:65769502..65771694,2	K562	blood:
34	chr11:65759257..65761081-chr11:65768976..65770919,2	MCF-7	breast:
35	chr11:65761975..65763785-chr11:65767733..65769368,2	MCF-7	breast:
36	chr11:65626559..65628548-chr11:65757169..65758764,2	MCF-7	breast:
37	chr11:65762401..65764466-chr11:65772379..65774986,2	K562	blood:
38	chr11:65755754..65758071-chr11:65759625..65762366,2	K562	blood:
39	chr11:65757124..65758738-chr11:65818489..65820917,2	K562	blood:
40	chr11:65749395..65751656-chr11:65763529..65766422,3	K562	blood:
41	chr11:65755935..65759042-chr11:65762460..65765703,3	MCF-7	breast:
42	chr11:65758842..65760410-chr11:65788361..65790977,2	MCF-7	breast:

No data

Variant related genes	Relation type
BANF1	TF binding region
ENSG00000238752	chromatin interactions
ENSG00000175334	chromatin interactions
ENSG00000172663	chromatin interactions
ENSG00000175602	chromatin interactions
ENSG00000172977	chromatin interactions
ENSG00000255038	chromatin interactions
ENSG00000175376	chromatin interactions
ENSG00000175550	chromatin interactions
ENSG00000087365	chromatin interactions
ENSG00000175573	chromatin interactions
ENSG00000254867	chromatin interactions
ENSG00000172757	chromatin interactions
ENSG00000172732	chromatin interactions
ENSG00000175294	chromatin interactions
ENSG00000172500	chromatin interactions
ENSG00000175467	chromatin interactions

Extended variants
information (count: 278 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:278 , 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	rs542524115	chr11:65757861-65757862	Weak transcription Strong transcription	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
2	rs562333724	chr11:65757862-65757863	Weak transcription Strong transcription	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
3	rs141871632	chr11:65757878-65757879	Weak transcription Strong transcription	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
4	rs200025541	chr11:65757881-65757882	Weak transcription Strong transcription	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
5	rs72930905	chr11:65757892-65757893	Weak transcription Strong transcription	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
6	rs547347406	chr11:65757911-65757912	Weak transcription Strong transcription	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
7	rs376987279	chr11:65757912-65757913	Weak transcription Strong transcription	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
8	rs530832331	chr11:65757913-65757914	Weak transcription Strong transcription	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
9	rs544546027	chr11:65757915-65757916	Weak transcription Strong transcription	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
10	rs532161679	chr11:65757919-65757920	Weak transcription Strong transcription	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
11	rs75677392	chr11:65757969-65757970	Weak transcription Strong transcription	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
12	rs111260968	chr11:65758031-65758032	Weak transcription Strong transcription	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
13	rs138051195	chr11:65758283-65758284	Weak transcription Strong transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
14	rs114349188	chr11:65758289-65758290	Weak transcription Strong transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
15	rs529187306	chr11:65758311-65758312	Weak transcription Strong transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
16	rs376278852	chr11:65758326-65758327	Weak transcription Strong transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
17	rs552154244	chr11:65758339-65758340	Weak transcription Strong transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
18	rs548884253	chr11:65758344-65758345	Weak transcription Strong transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
19	rs149516544	chr11:65758375-65758376	Weak transcription Strong transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
20	rs531099963	chr11:65758402-65758403	Weak transcription Strong transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
21	rs557695240	chr11:65758416-65758417	Weak transcription Strong transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
22	rs369458759	chr11:65758433-65758434	Weak transcription Strong transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
23	rs370312678	chr11:65758440-65758441	Weak transcription Strong transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
24	rs571296097	chr11:65758444-65758445	Weak transcription Strong transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
25	rs533883801	chr11:65758445-65758446	Weak transcription Strong transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
26	rs551198982	chr11:65758454-65758455	Weak transcription Strong transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
27	rs553635992	chr11:65758475-65758476	Weak transcription Strong transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
28	rs567736808	chr11:65758484-65758485	Weak transcription Strong transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
29	rs573490803	chr11:65758504-65758505	Weak transcription Strong transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
30	rs536029850	chr11:65758508-65758509	Weak transcription Strong transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
31	rs75260268	chr11:65758583-65758584	Weak transcription Strong transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
32	rs371923276	chr11:65758600-65758601	Weak transcription Strong transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
33	rs575851515	chr11:65758658-65758659	Weak transcription Strong transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
34	rs76691101	chr11:65758674-65758675	Weak transcription Strong transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
35	rs564500317	chr11:65758678-65758679	Weak transcription Strong transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
36	rs180820418	chr11:65758686-65758687	Weak transcription Strong transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
37	rs186240053	chr11:65758699-65758700	Weak transcription Strong transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
38	rs560180776	chr11:65758716-65758717	Weak transcription Strong transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
39	rs386754413	chr11:65758717-65758718	Weak transcription Strong transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
40	rs536787362	chr11:65758749-65758750	Weak transcription Strong transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
41	rs548722334	chr11:65758771-65758772	Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs376382440	chr11:65758779-65758780	Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs562650184	chr11:65758806-65758807	Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs80317198	chr11:65758808-65758809	Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs190800392	chr11:65758846-65758847	Weak transcription Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
46	rs1151514	chr11:65758854-65758855	Weak transcription Strong transcription	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs533734236	chr11:65758895-65758896	Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs547536977	chr11:65758910-65758911	Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs567322856	chr11:65758922-65758923	Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs183948783	chr11:65758924-65758925	Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:99)

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
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Pituitary adenoma	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Metanephric adenoma	20802469	CNVD
Chordoma	21602918	CNVD
Melanoma	18172304	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
ovarian endometriomas	16273235	CNVD
Breast cancer	16417655	CNVD
Myelofibrosis	22110671	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Prostate cancer	17217626	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	21045282	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
Anaplastic thyroid cancer	18753363	CNVD
Prostate cancer	18779856	CNVD
Cancer	17160897	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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:275 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:65730600-65767800	Weak transcription	Right Atrium	heart
2	chr11:65736400-65767400	Weak transcription	Psoas Muscle	Psoas
3	chr11:65741200-65765000	Weak transcription	NHDF-Ad	bronchial
4	chr11:65741400-65762000	Weak transcription	HSMMtube	muscle
5	chr11:65741600-65762000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr11:65742200-65759800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr11:65743800-65764800	Weak transcription	HSMM	muscle
8	chr11:65745000-65764200	Weak transcription	HUVEC	blood vessel
9	chr11:65745200-65764800	Weak transcription	K562	blood
10	chr11:65745400-65764800	Weak transcription	Rectal Smooth Muscle	rectum
11	chr11:65745400-65765000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr11:65745600-65764200	Weak transcription	NH-A	brain
13	chr11:65745800-65764800	Weak transcription	Primary hematopoietic stem cells	blood
14	chr11:65746000-65764600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr11:65746800-65765000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr11:65747000-65764200	Weak transcription	Muscle Satellite Cultured Cells	--
17	chr11:65747000-65764600	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr11:65747000-65764600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
19	chr11:65747000-65764600	Weak transcription	Ovary	ovary
20	chr11:65747000-65764800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
21	chr11:65747200-65759800	Weak transcription	Lung	lung
22	chr11:65747200-65764200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
23	chr11:65747200-65764200	Weak transcription	Adipose Nuclei	Adipose
24	chr11:65747200-65764200	Weak transcription	Liver	Liver
25	chr11:65747200-65764200	Weak transcription	A549	lung
26	chr11:65747200-65764400	Weak transcription	Left Ventricle	heart
27	chr11:65747200-65764600	Weak transcription	H1 Cell Line	embryonic stem cell
28	chr11:65747200-65764600	Weak transcription	Brain Hippocampus Middle	brain
29	chr11:65747200-65764800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
30	chr11:65747200-65764800	Weak transcription	Pancreas	Pancrea
31	chr11:65747200-65764800	Weak transcription	Small Intestine	intestine
32	chr11:65747400-65763000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
33	chr11:65747400-65763800	Weak transcription	Primary T helper cells fromperipheralblood	blood
34	chr11:65747400-65764200	Weak transcription	Duodenum Smooth Muscle	Duodenum
35	chr11:65747400-65764200	Weak transcription	Sigmoid Colon	Sigmoid Colon
36	chr11:65747400-65764800	Weak transcription	HUES6 Cell Line	embryonic stem cell
37	chr11:65747400-65764800	Weak transcription	Fetal Lung	lung
38	chr11:65747400-65765200	Weak transcription	Placenta Amnion	Placenta Amnion
39	chr11:65747600-65764200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr11:65747600-65764600	Weak transcription	HUES64 Cell Line	embryonic stem cell
41	chr11:65747600-65764800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr11:65747600-65765000	Weak transcription	Colonic Mucosa	Colon
43	chr11:65747800-65762200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr11:65747800-65764000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr11:65747800-65764000	Weak transcription	Placenta	Placenta
46	chr11:65747800-65764200	Weak transcription	Gastric	stomach
47	chr11:65747800-65764200	Weak transcription	Right Ventricle	heart
48	chr11:65747800-65764200	Weak transcription	HMEC	breast
49	chr11:65747800-65764600	Weak transcription	Osteobl	bone
50	chr11:65747800-65764800	Weak transcription	H9 Cell Line	embryonic stem cell

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