Variant report

Variant	nsv8807
Chromosome Location	chr11:34912167-34930289
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:428)
CpG islands
(count:61)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:428 , 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	chr11:34912409-34912729	K562	blood:	n/a	n/a
2	ARID3A	chr11:34912499-34912747	HepG2	liver:	n/a	n/a
3	ATF3	chr11:34929799-34930110	K562	blood:	n/a	n/a
4	BACH1	chr11:34929538-34930075	H1-hESC	embryonic stem cell:	n/a	chr11:34929943-34929957
5	BACH1	chr11:34929700-34929782	K562	blood:	n/a	n/a
6	BATF	chr11:34929853-34930086	GM12878	blood:	n/a	chr11:34929946-34929957
7	BRCA1	chr11:34920613-34920873	Hela-S3	cervix:	n/a	n/a
8	BRCA1	chr11:34912447-34912805	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr11:34921297-34921703	A549	lung:	n/a	chr11:34921564-34921575
10	CEBPB	chr11:34927973-34928162	A549	lung:	n/a	chr11:34928076-34928087
11	CEBPB	chr11:34928015-34928209	HepG2	liver:	n/a	chr11:34928076-34928087
12	CEBPB	chr11:34928016-34928212	IMR90	lung:	n/a	chr11:34928076-34928087
13	CEBPB	chr11:34918324-34918454	HepG2	liver:	n/a	chr11:34918349-34918360
14	CEBPB	chr11:34928039-34928228	K562	blood:	n/a	chr11:34928076-34928087
15	CEBPB	chr11:34924848-34924975	HepG2	liver:	n/a	n/a
16	CEBPB	chr11:34921547-34921595	HepG2	liver:	n/a	chr11:34921564-34921575
17	CEBPB	chr11:34921467-34921725	K562	blood:	n/a	chr11:34921564-34921575
18	CTCF	chr11:34924594-34924633	GM12878	blood:	n/a	n/a
19	CTCF	chr11:34920700-34920850	SK-N-SH_RA	brain:	n/a	n/a
20	CTCF	chr11:34921080-34921230	NHEK	skin:	n/a	n/a
21	CTCF	chr11:34920602-34920855	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr11:34912760-34912910	HAc	cerebellar:	n/a	n/a
23	CTCF	chr11:34912520-34912670	K562	blood:	n/a	chr11:34912574-34912592
24	CTCF	chr11:34912520-34912670	AG10803	skin:	n/a	chr11:34912574-34912592
25	CTCF	chr11:34912500-34912650	AG04449	skin:	n/a	chr11:34912574-34912592
26	CTCF	chr11:34920680-34920849	LNCaP	prostate:	n/a	n/a
27	CTCF	chr11:34920720-34920870	AG10803	skin:	n/a	n/a
28	CTCF	chr11:34912540-34912690	HPF	lung:	n/a	chr11:34912574-34912592
29	CTCF	chr11:34920720-34920870	NHLF	lung:	n/a	n/a
30	CTCF	chr11:34920740-34920890	HRPEpiC	eye:	n/a	n/a
31	CTCF	chr11:34920680-34920840	LNCaP	prostate:	n/a	n/a
32	CTCF	chr11:34920740-34920890	HCM	heart:	n/a	n/a
33	CTCF	chr11:34920700-34920850	HPF	lung:	n/a	n/a
34	CTCF	chr11:34920720-34920870	NHEK	skin:	n/a	n/a
35	CTCF	chr11:34920733-34920790	ProgFib	skin:	n/a	n/a
36	CTCF	chr11:34920640-34920790	K562	blood:	n/a	n/a
37	CTCF	chr11:34920700-34920850	HMF	breast:	n/a	n/a
38	CTCF	chr11:34911414-34913598	A549	lung:	n/a	chr11:34911824-34911845 chr11:34912574-34912592
39	CTCF	chr11:34912382-34912694	MCF-7	breast:	n/a	chr11:34912574-34912592
40	CTCF	chr11:34912500-34912691	GM12878	blood:	n/a	chr11:34912574-34912592
41	CTCF	chr11:34912505-34912675	LNCaP	prostate:	n/a	chr11:34912574-34912592
42	CTCF	chr11:34920760-34920910	BJ	skin:	n/a	n/a
43	CTCF	chr11:34912451-34912750	H1-hESC	embryonic stem cell:	n/a	chr11:34912574-34912592
44	CTCF	chr11:34912500-34912650	SK-N-SH_RA	brain:	n/a	chr11:34912574-34912592
45	CTCF	chr11:34913300-34913450	GM12864	blood:	n/a	n/a
46	CTCF	chr11:34920700-34920850	AG04450	lung:	n/a	n/a
47	CTCF	chr11:34920562-34920910	K562	blood:	n/a	n/a
48	CTCF	chr11:34912480-34912630	SAEC	small airway:	n/a	chr11:34912574-34912592
49	CTCF	chr11:34920720-34920870	WERI-Rb-1	eye:	n/a	n/a
50	CTCF	chr11:34920740-34920890	AG09319	gingival:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:34929792-34929842	HAEpiC	amniotic membrane:	n/a
2	chr11:34929792-34929842	GM06990	blood:	n/a
3	chr11:34929792-34929842	LNCaP	prostate:	n/a
4	chr11:34929792-34929842	NB4	blood:	n/a
5	chr11:34929792-34929842	T-47D	breast:	n/a
6	chr11:34929792-34929842	HEK293	kidney:	embryo
7	chr11:34929792-34929842	HIPEpiC	eye:	n/a
8	chr11:34929792-34929842	HNPCEpiC	eye:	n/a
9	chr11:34929792-34929842	NHDF-neo	bronchial:	n/a
10	chr11:34929792-34929842	HUVEC	blood vessel:	n/a
11	chr11:34929792-34929842	AoSMC	blood vessel:	n/a
12	chr11:34929792-34929842	GM12892	blood:	n/a
13	chr11:34929792-34929842	PANC-1	pancreas:	n/a
14	chr11:34929792-34929842	GM12891	blood:	n/a
15	chr11:34929792-34929842	ProgFib	skin:	n/a
16	chr11:34929792-34929842	IMR90	lung:	fetal
17	chr11:34929792-34929842	SAEC	small airway:	n/a
18	chr11:34929792-34929842	AG09319	gingival:	n/a
19	chr11:34929792-34929842	HL-60	blood:	n/a
20	chr11:34929792-34929842	K562	blood:	n/a
21	chr11:34929792-34929842	HCPEpiC	choroid plexus:	n/a
22	chr11:34929792-34929842	HCF	heart:	n/a
23	chr11:34929792-34929842	RPTEC	kidney:	n/a
24	chr11:34929792-34929842	AG10803	skin:	n/a
25	chr11:34929792-34929842	HRE	kidney:	n/a
26	chr11:34929792-34929842	H1-hESC	embryonic stem cell:	embryo
27	chr11:34929792-34929842	HMEC	breast:	n/a
28	chr11:34929792-34929842	NH-A	brain:	n/a
29	chr11:34929792-34929842	HRPEpiC	eye:	n/a
30	chr11:34929792-34929842	BE2_C	brain:	n/a
31	chr11:34929792-34929842	BJ	skin:	n/a
32	chr11:34929792-34929842	Hela-S3	cervix:	n/a
33	chr11:34929792-34929842	NT2-D1	testis:	n/a
34	chr11:34929792-34929842	AG09309	skin:	n/a
35	chr11:34929792-34929842	AG04449	skin:	fetal
36	chr11:34929792-34929842	GM12878	blood:	n/a
37	chr11:34929792-34929842	HCM	heart:	n/a
38	chr11:34929792-34929842	SK-N-SH	brain:	n/a
39	chr11:34929792-34929842	HepG2	liver:	n/a
40	chr11:34929792-34929842	HCT-116	colon:	n/a
41	chr11:34929792-34929842	MCF10A-Er-Src	breast:	n/a
42	chr11:34929792-34929842	SKMC	muscle:	n/a
43	chr11:34929792-34929842	ECC-1	luminal epithelium:	n/a
44	chr11:34929792-34929842	MCF-7	breast:	n/a
45	chr11:34929792-34929842	A549	lung:	n/a
46	chr11:34929792-34929842	PrEC	prostate:	n/a
47	chr11:34929792-34929842	AG04450	lung:	fetal
48	chr11:34929792-34929842	SK-N-MC	brain:	n/a
49	chr11:34929792-34929842	Caco-2	colon:	n/a
50	chr11:34929792-34929842	U87	brain:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:34928494..34930891-chr11:34936071..34939196,3	MCF-7	breast:
2	chr11:34607165..34608016-chr11:34920268..34920858,2	K562	blood:
3	chr11:34919773..34921558-chr11:34929230..34931688,2	K562	blood:
4	chr11:34534104..34535140-chr11:34920268..34920796,4	K562	blood:
5	chr11:34923546..34926678-chr11:34933429..34938581,5	MCF-7	breast:
6	chr11:34588812..34589630-chr11:34920341..34921212,2	K562	blood:
7	chr11:34921303..34922935-chr11:34924601..34927346,2	MCF-7	breast:
8	chr11:34923966..34926335-chr11:34931824..34933676,2	K562	blood:
9	chr11:34919773..34921558-chr11:34929230..34931688,2	K562	blood:
10	chr11:34891442..34894035-chr11:34912560..34915333,2	K562	blood:
11	chr11:34905872..34908385-chr11:34915875..34918496,2	K562	blood:
12	chr11:34927454..34929735-chr11:34930952..34932783,2	K562	blood:
13	chr11:34928718..34934554-chr11:34935181..34939232,15	MCF-7	breast:
14	chr11:34921303..34922935-chr11:34924601..34927346,2	MCF-7	breast:
15	chr11:34926486..34928206-chr11:36379103..36382037,2	K562	blood:

No data

Variant related genes	Relation type
APIP	TF binding region
APIP	CpG island
ENSG00000110435	chromatin interactions
ENSG00000149089	chromatin interactions

Extended variants
information (count: 667 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:667 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561001814	chr11:34912210-34912211	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs573967417	chr11:34912239-34912240	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs536554600	chr11:34912241-34912242	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs2915224	chr11:34912289-34912290	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs576554071	chr11:34912292-34912293	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs545632406	chr11:34912420-34912421	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs190643517	chr11:34912516-34912517	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs572605035	chr11:34912567-34912568	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs35733050	chr11:34912630-34912631	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs541399992	chr11:34912649-34912650	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs561285572	chr11:34912652-34912653	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs182987068	chr11:34912669-34912670	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs187658269	chr11:34912717-34912718	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs75877363	chr11:34912823-34912824	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs1430856	chr11:34912861-34912862	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs146109294	chr11:34912876-34912877	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs148797667	chr11:34912882-34912883	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs1430855	chr11:34912908-34912909	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs78476784	chr11:34912918-34912919	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs578156223	chr11:34913016-34913017	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs566935488	chr11:34913032-34913033	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs192686411	chr11:34913055-34913056	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs117623336	chr11:34913125-34913126	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs570354404	chr11:34913129-34913130	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs2985389	chr11:34913164-34913165	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs531090229	chr11:34913201-34913202	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs376449439	chr11:34913202-34913203	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs559208586	chr11:34913212-34913213	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs141600173	chr11:34913262-34913263	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs112195172	chr11:34913264-34913265	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs2985388	chr11:34913265-34913266	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs567394315	chr11:34913299-34913300	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs3751078	chr11:34913315-34913316	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs543844830	chr11:34913322-34913323	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs528576179	chr11:34913333-34913334	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs184744021	chr11:34913340-34913341	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs531651294	chr11:34913460-34913461	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs544849043	chr11:34913465-34913466	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs187217513	chr11:34913488-34913489	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs547025772	chr11:34913513-34913514	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs573766793	chr11:34913556-34913557	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs547083647	chr11:34913582-34913583	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs567071869	chr11:34913584-34913585	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs529638038	chr11:34913593-34913594	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs549781163	chr11:34913627-34913628	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs570217996	chr11:34913632-34913633	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs539338858	chr11:34913647-34913648	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs571648046	chr11:34913724-34913725	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs559144627	chr11:34913737-34913738	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs566286883	chr11:34913764-34913765	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:456 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:34882000-34919800	Weak transcription	Left Ventricle	heart
2	chr11:34891200-34919200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr11:34892600-34913000	Weak transcription	Brain Anterior Caudate	brain
4	chr11:34893000-34921400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr11:34895000-34921200	Weak transcription	Right Ventricle	heart
6	chr11:34896000-34912200	Weak transcription	K562	blood
7	chr11:34897000-34913000	Weak transcription	Lung	lung
8	chr11:34897000-34919200	Weak transcription	Fetal Stomach	stomach
9	chr11:34897600-34919200	Weak transcription	Fetal Heart	heart
10	chr11:34898200-34926800	Weak transcription	HSMMtube	muscle
11	chr11:34898400-34912800	Weak transcription	Brain Hippocampus Middle	brain
12	chr11:34899000-34917400	Weak transcription	HSMM	muscle
13	chr11:34900000-34918200	Weak transcription	Cortex derived primary cultured neurospheres	brain
14	chr11:34900200-34917200	Weak transcription	HUVEC	blood vessel
15	chr11:34900200-34921000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr11:34901400-34917400	Weak transcription	Fetal Kidney	kidney
17	chr11:34901400-34920800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr11:34901600-34918200	Weak transcription	Primary neutrophils fromperipheralblood	blood
19	chr11:34901800-34916800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
20	chr11:34901800-34917000	Weak transcription	Rectal Mucosa Donor 29	rectum
21	chr11:34902000-34921600	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr11:34902200-34915600	Weak transcription	Colon Smooth Muscle	Colon
23	chr11:34902400-34912800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr11:34903600-34919200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr11:34903800-34914200	Weak transcription	Fetal Brain Male	brain
26	chr11:34904000-34918600	Weak transcription	NHDF-Ad	bronchial
27	chr11:34904800-34915600	Weak transcription	GM12878-XiMat	blood
28	chr11:34905000-34912800	Weak transcription	Primary B cells from cord blood	blood
29	chr11:34905000-34917800	Weak transcription	HUES6 Cell Line	embryonic stem cell
30	chr11:34905200-34912600	Weak transcription	Primary hematopoietic stem cells	blood
31	chr11:34905200-34912800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr11:34905200-34915200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr11:34905200-34915400	Weak transcription	Fetal Brain Female	brain
34	chr11:34905200-34917800	Weak transcription	Primary B cells from peripheral blood	blood
35	chr11:34906200-34916200	Weak transcription	Primary T cells from cord blood	blood
36	chr11:34907200-34918200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr11:34907400-34917800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
38	chr11:34907600-34912200	Weak transcription	Brain Inferior Temporal Lobe	brain
39	chr11:34907800-34918000	Weak transcription	Fetal Intestine Large	intestine
40	chr11:34908400-34921200	Weak transcription	Aorta	Aorta
41	chr11:34908600-34917800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr11:34908800-34912200	Weak transcription	HUES48 Cell Line	embryonic stem cell
43	chr11:34908800-34915600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
44	chr11:34908800-34921000	Weak transcription	Ovary	ovary
45	chr11:34909000-34915000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
46	chr11:34909200-34912800	Weak transcription	HepG2	liver
47	chr11:34909200-34919200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
48	chr11:34909400-34918200	Weak transcription	Duodenum Smooth Muscle	Duodenum
49	chr11:34909600-34918200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
50	chr11:34909800-34921600	Weak transcription	Stomach Mucosa	stomach

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