Variant report

Variant	nsv1042924
Chromosome Location	chr11:76659477-76709407
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:151)
CpG islands
(count:61)
Chromatin interactive
region (count:15)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:151 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:76673985-76674672	HepG2	liver:	n/a	n/a
2	ATF1	chr11:76698288-76698423	K562	blood:	n/a	n/a
3	BHLHE40	chr11:76674211-76674319	GM12878	blood:	n/a	n/a
4	CBX3	chr11:76683051-76683513	HCT-116	colon:	n/a	n/a
5	CBX3	chr11:76689231-76689598	K562	blood:	n/a	n/a
6	CEBPB	chr11:76661518-76661703	HepG2	liver:	n/a	chr11:76661561-76661572
7	CEBPB	chr11:76663683-76663784	IMR90	lung:	n/a	n/a
8	CEBPB	chr11:76661504-76661691	IMR90	lung:	n/a	chr11:76661561-76661572
9	CEBPB	chr11:76661695-76661696	A549	lung:	n/a	n/a
10	CEBPB	chr11:76661526-76661690	K562	blood:	n/a	chr11:76661561-76661572
11	CEBPB	chr11:76684751-76684965	K562	blood:	n/a	n/a
12	CEBPB	chr11:76663526-76664088	HepG2	liver:	n/a	n/a
13	CEBPD	chr11:76673965-76674262	HepG2	liver:	n/a	n/a
14	CHD1	chr11:76681188-76681323	GM12878	blood:	n/a	n/a
15	CTCF	chr11:76685289-76685392	MCF-7	breast:	n/a	n/a
16	CTCF	chr11:76685351-76685417	Hela-S3	cervix:	n/a	n/a
17	CTCF	chr11:76685460-76685610	HMEC	breast:	n/a	n/a
18	CTCF	chr11:76671860-76672010	Caco-2	colon:	n/a	n/a
19	CTCF	chr11:76685322-76685471	Pancreas_OC	pancreas:	n/a	n/a
20	CTCF	chr11:76684499-76684553	Fibrobl	skin:	n/a	n/a
21	CTCF	chr11:76683700-76683850	HepG2	liver:	n/a	chr11:76683828-76683838
22	E2F4	chr11:76682707-76682759	MCF10A-Er-Src	breast:	n/a	n/a
23	E2F4	chr11:76685046-76685172	MCF10A-Er-Src	breast:	n/a	n/a
24	ELF1	chr11:76674055-76674370	HepG2	liver:	n/a	n/a
25	ELF1	chr11:76673960-76674413	HepG2	liver:	n/a	n/a
26	ELF1	chr11:76695803-76696213	MCF-7	breast:	n/a	n/a
27	EP300	chr11:76698234-76698549	K562	blood:	n/a	n/a
28	EP300	chr11:76674084-76674415	HepG2	liver:	n/a	n/a
29	EP300	chr11:76673899-76674555	HepG2	liver:	n/a	n/a
30	EP300	chr11:76673850-76674482	HepG2	liver:	n/a	n/a
31	EP300	chr11:76674113-76674347	GM12878	blood:	n/a	n/a
32	FOS	chr11:76666709-76667006	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr11:76686596-76686864	MCF10A-Er-Src	breast:	n/a	chr11:76686756-76686764
34	FOSL2	chr11:76673991-76674386	HepG2	liver:	n/a	n/a
35	FOSL2	chr11:76673961-76674364	HepG2	liver:	n/a	n/a
36	FOXA1	chr11:76698704-76699067	HepG2	liver:	n/a	n/a
37	FOXA1	chr11:76673966-76674734	HepG2	liver:	n/a	n/a
38	FOXA1	chr11:76698825-76699151	HepG2	liver:	n/a	n/a
39	FOXA1	chr11:76673864-76674565	HepG2	liver:	n/a	n/a
40	FOXA1	chr11:76698729-76699082	HepG2	liver:	n/a	n/a
41	FOXA1	chr11:76673920-76674714	HepG2	liver:	n/a	n/a
42	FOXA1	chr11:76673906-76674689	HepG2	liver:	n/a	n/a
43	FOXA1	chr11:76698795-76699180	HepG2	liver:	n/a	n/a
44	FOXA2	chr11:76675184-76675558	A549	lung:	n/a	n/a
45	FOXA2	chr11:76698803-76699046	HepG2	liver:	n/a	n/a
46	FOXA2	chr11:76673955-76674693	HepG2	liver:	n/a	n/a
47	FOXA2	chr11:76673840-76674809	HepG2	liver:	n/a	n/a
48	GATA2	chr11:76698228-76698621	K562	blood:	n/a	n/a
49	GATA3	chr11:76673753-76674450	MCF-7	breast:	n/a	chr11:76674112-76674120
50	GATA3	chr11:76673855-76674344	MCF-7	breast:	n/a	chr11:76674112-76674120

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:76709256-76709306	MCF10A-Er-Src	breast:	n/a
2	chr11:76709256-76709306	NT2-D1	testis:	n/a
3	chr11:76709256-76709306	HIPEpiC	eye:	n/a
4	chr11:76709256-76709306	Jurkat	blood:	n/a
5	chr11:76709256-76709306	PFSK-1	brain:	n/a
6	chr11:76709256-76709306	GM12892	blood:	n/a
7	chr11:76709256-76709306	NHDF-neo	bronchial:	n/a
8	chr11:76709256-76709306	SK-N-MC	brain:	n/a
9	chr11:76709256-76709306	PANC-1	pancreas:	n/a
10	chr11:76709256-76709306	H1-hESC	embryonic stem cell:	embryo
11	chr11:76709256-76709306	Caco-2	colon:	n/a
12	chr11:76709256-76709306	T-47D	breast:	n/a
13	chr11:76709256-76709306	GM06990	blood:	n/a
14	chr11:76709256-76709306	BJ	skin:	n/a
15	chr11:76709256-76709306	AG10803	skin:	n/a
16	chr11:76709256-76709306	ECC-1	luminal epithelium:	n/a
17	chr11:76709256-76709306	HL-60	blood:	n/a
18	chr11:76709256-76709306	HRPEpiC	eye:	n/a
19	chr11:76709256-76709306	ProgFib	skin:	n/a
20	chr11:76709256-76709306	LNCaP	prostate:	n/a
21	chr11:76709256-76709306	NB4	blood:	n/a
22	chr11:76709256-76709306	HEK293	kidney:	embryo
23	chr11:76709256-76709306	Hepatocyte	liver:	n/a
24	chr11:76709256-76709306	NHBE	bronchial:	n/a
25	chr11:76709256-76709306	AG04450	lung:	fetal
26	chr11:76709256-76709306	HAEpiC	amniotic membrane:	n/a
27	chr11:76709256-76709306	HEEpiC	esophagus:	n/a
28	chr11:76709256-76709306	U87	brain:	n/a
29	chr11:76709256-76709306	Hela-S3	cervix:	n/a
30	chr11:76709256-76709306	K562	blood:	n/a
31	chr11:76709256-76709306	HNPCEpiC	eye:	n/a
32	chr11:76709256-76709306	PrEC	prostate:	n/a
33	chr11:76709256-76709306	HepG2	liver:	n/a
34	chr11:76709256-76709306	HUVEC	blood vessel:	n/a
35	chr11:76709256-76709306	HRCEpiC	kidney:	n/a
36	chr11:76709256-76709306	SK-N-SH_RA	brain:	n/a
37	chr11:76709256-76709306	HCPEpiC	choroid plexus:	n/a
38	chr11:76709256-76709306	BE2_C	brain:	n/a
39	chr11:76709256-76709306	HPAEpiC	pulmonary alveolar:	n/a
40	chr11:76709256-76709306	ovcar-3	ovarian:	n/a
41	chr11:76709256-76709306	AG09309	skin:	n/a
42	chr11:76709256-76709306	AoSMC	blood vessel:	n/a
43	chr11:76709256-76709306	SKMC	muscle:	n/a
44	chr11:76709256-76709306	HRE	kidney:	n/a
45	chr11:76709256-76709306	HCT-116	colon:	n/a
46	chr11:76709256-76709306	HCM	heart:	n/a
47	chr11:76709256-76709306	SAEC	small airway:	n/a
48	chr11:76709256-76709306	A549	lung:	n/a
49	chr11:76709256-76709306	AG09319	gingival:	n/a
50	chr11:76709256-76709306	RPTEC	kidney:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr11:76686294..76687888-chr11:76690773..76692768,2	K562	blood:
2	chr11:76666896..76668570-chr11:76671083..76673989,2	K562	blood:
3	chr11:76684953..76685685-chr11:76756997..76757683,2	MCF-7	breast:
4	chr11:76691341..76694336-chr11:76696975..76699945,2	K562	blood:
5	chr11:76691402..76695270-chr11:76696975..76699875,3	K562	blood:
6	chr11:76653898..76657828-chr11:76664691..76666325,3	K562	blood:
7	chr11:76693879..76696563-chr11:76699673..76701721,2	MCF-7	breast:
8	chr11:76691341..76694336-chr11:76696975..76699945,2	K562	blood:
9	chr11:76693879..76696563-chr11:76699673..76701721,2	MCF-7	breast:
10	chr11:76630886..76632771-chr11:76660350..76662030,2	K562	blood:
11	chr11:76684575..76686730-chr11:76722373..76724667,2	MCF-7	breast:
12	chr11:76666896..76668570-chr11:76671083..76673989,2	K562	blood:
13	chr11:76699145..76701750-chr11:76703493..76705984,2	K562	blood:
14	chr11:76686294..76687888-chr11:76690773..76692768,2	K562	blood:
15	chr11:76691402..76695270-chr11:76696975..76699875,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GDPD4-2	chr11:76669878-76670057	ENSG00000254988.1
2	lnc-GDPD4-2	chr11:76689445-76689663	ENSG00000254988.1
3	lnc-GDPD4-2	chr11:76666461-76666629	ENSG00000254988.1

No data

Variant related genes	Relation type
ACER3	TF binding region
ENSG00000254988	TF binding region
ACER3	CpG island
ENSG00000254988	CpG island
ENSG00000078124	chromatin interactions

Extended variants
information (count: 1739 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:1739 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs546309067	chr11:76659555-76659556	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs60521259	chr11:76659596-76659597	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs145474739	chr11:76659600-76659601	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs542014089	chr11:76659604-76659605	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs12222825	chr11:76659609-76659610	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs141223521	chr11:76659643-76659644	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs75823826	chr11:76659658-76659659	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs563731914	chr11:76659677-76659678	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs185529625	chr11:76659819-76659820	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs532109717	chr11:76659828-76659829	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs549754612	chr11:76659966-76659967	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs10431154	chr11:76660019-76660020	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs10431182	chr11:76660088-76660089	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs548877862	chr11:76660094-76660095	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs529702639	chr11:76660098-76660099	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs202033062	chr11:76660120-76660121	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs77424765	chr11:76660124-76660125	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs66957458	chr11:76660125-76660126	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs372801036	chr11:76660126-76660127	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs397818802	chr11:76660127-76660128	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs199497653	chr11:76660128-76660129	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs57908416	chr11:76660180-76660181	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs534899805	chr11:76660358-76660359	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs558123345	chr11:76660361-76660362	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs10899331	chr11:76660366-76660367	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs188960060	chr11:76660410-76660411	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs181715621	chr11:76660419-76660420	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs535984292	chr11:76660437-76660438	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs367784813	chr11:76660438-76660439	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs146967326	chr11:76660445-76660446	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs542328801	chr11:76660452-76660453	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs11237027	chr11:76660458-76660459	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs147590968	chr11:76660471-76660472	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs185843159	chr11:76660474-76660475	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs548561592	chr11:76660493-76660494	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs570938556	chr11:76660555-76660556	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs535097448	chr11:76660576-76660577	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs535839507	chr11:76660612-76660613	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs564392475	chr11:76660613-76660614	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs7104807	chr11:76660621-76660622	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs553008465	chr11:76660645-76660646	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs145360418	chr11:76660647-76660648	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs142120898	chr11:76660666-76660667	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs376242282	chr11:76660676-76660677	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs563318570	chr11:76660771-76660772	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs7118970	chr11:76660780-76660781	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs56789915	chr11:76660793-76660794	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs554563551	chr11:76660797-76660798	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs559577058	chr11:76660804-76660805	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs188691996	chr11:76660863-76660864	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

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
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
Melanoma	18172304	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
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Breast cancer	16620391	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21482786	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	16608533	CNVD
Usher syndrome	18421352	CNVD
Ovarian cancer	21240255	CNVD
Ovarian cancer	22355333	CNVD
Breast cancer	20932292	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Cancer	20164920	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Acute lymphoblastic leukemia	17690704	CNVD

Chromatin state (count:667 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:76631400-76688400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr11:76631600-76670200	Weak transcription	Left Ventricle	heart
3	chr11:76631600-76671600	Weak transcription	Ovary	ovary
4	chr11:76644000-76666400	Weak transcription	NHEK	skin
5	chr11:76645800-76683800	Weak transcription	Esophagus	oesophagus
6	chr11:76646200-76670600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
7	chr11:76646600-76688000	Weak transcription	HMEC	breast
8	chr11:76647000-76670200	Weak transcription	Primary neutrophils fromperipheralblood	blood
9	chr11:76647200-76671600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr11:76647200-76673800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr11:76647200-76674800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr11:76647400-76670000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr11:76648400-76671600	Weak transcription	Spleen	Spleen
14	chr11:76649600-76669600	Weak transcription	Primary monocytes fromperipheralblood	blood
15	chr11:76649600-76672000	Weak transcription	Aorta	Aorta
16	chr11:76650000-76669600	Weak transcription	Adipose Nuclei	Adipose
17	chr11:76650600-76670000	Weak transcription	Placenta	Placenta
18	chr11:76650600-76681200	Weak transcription	Brain Substantia Nigra	brain
19	chr11:76655800-76666400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr11:76655800-76671600	Weak transcription	Brain Inferior Temporal Lobe	brain
21	chr11:76655800-76674200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr11:76655800-76681800	Weak transcription	Primary B cells from cord blood	blood
23	chr11:76656200-76677000	Weak transcription	Brain Anterior Caudate	brain
24	chr11:76656400-76671200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr11:76656800-76670000	Weak transcription	Cortex derived primary cultured neurospheres	brain
26	chr11:76657000-76670200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
27	chr11:76657000-76674600	Weak transcription	Fetal Stomach	stomach
28	chr11:76657000-76676600	Weak transcription	Primary B cells from peripheral blood	blood
29	chr11:76657200-76688400	Weak transcription	Gastric	stomach
30	chr11:76657400-76659800	Weak transcription	Monocytes-CD14+_RO01746	blood
31	chr11:76657400-76663800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
32	chr11:76657400-76670200	Weak transcription	Sigmoid Colon	Sigmoid Colon
33	chr11:76657600-76669600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr11:76657600-76671600	Weak transcription	Lung	lung
35	chr11:76657600-76672600	Weak transcription	Brain Germinal Matrix	brain
36	chr11:76657800-76669600	Weak transcription	Stomach Mucosa	stomach
37	chr11:76658200-76659600	Weak transcription	Fetal Intestine Small	intestine
38	chr11:76658200-76666600	Weak transcription	Hela-S3	cervix
39	chr11:76658400-76659800	Enhancers	Primary T cells from cord blood	blood
40	chr11:76659000-76660000	Enhancers	Fetal Intestine Large	intestine
41	chr11:76659200-76659600	Enhancers	Small Intestine	intestine
42	chr11:76659200-76659800	Enhancers	Duodenum Mucosa	Duodenum
43	chr11:76659600-76659800	Enhancers	Rectal Mucosa Donor 29	rectum
44	chr11:76659600-76660200	Enhancers	Fetal Intestine Small	intestine
45	chr11:76659600-76673600	Weak transcription	Small Intestine	intestine
46	chr11:76659800-76661200	Strong transcription	Monocytes-CD14+_RO01746	blood
47	chr11:76659800-76669800	Weak transcription	Rectal Mucosa Donor 29	rectum
48	chr11:76659800-76673400	Weak transcription	Duodenum Mucosa	Duodenum
49	chr11:76659800-76673600	Weak transcription	Primary T cells from cord blood	blood
50	chr11:76660000-76664000	Weak transcription	Fetal Intestine Large	intestine

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