Variant report

Variant	nsv519700
Chromosome Location	chr11:76637651-76709407
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:254)
CpG islands
(count:183)
Chromatin interactive
region (count:19)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:254 , 50 per page) page: 1 2 3 4 5 6

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	ARID3A	chr11:76650140-76650484	HepG2	liver:	n/a	n/a
3	ATF1	chr11:76698288-76698423	K562	blood:	n/a	n/a
4	BHLHE40	chr11:76674211-76674319	GM12878	blood:	n/a	n/a
5	CBX3	chr11:76689231-76689598	K562	blood:	n/a	n/a
6	CBX3	chr11:76683051-76683513	HCT-116	colon:	n/a	n/a
7	CBX3	chr11:76646052-76646517	HCT-116	colon:	n/a	n/a
8	CEBPB	chr11:76663683-76663784	IMR90	lung:	n/a	n/a
9	CEBPB	chr11:76663526-76664088	HepG2	liver:	n/a	n/a
10	CEBPB	chr11:76661518-76661703	HepG2	liver:	n/a	chr11:76661561-76661572
11	CEBPB	chr11:76649094-76649136	K562	blood:	n/a	chr11:76649114-76649125
12	CEBPB	chr11:76648985-76649285	HepG2	liver:	n/a	chr11:76649114-76649125
13	CEBPB	chr11:76661526-76661690	K562	blood:	n/a	chr11:76661561-76661572
14	CEBPB	chr11:76684751-76684965	K562	blood:	n/a	n/a
15	CEBPB	chr11:76650275-76650395	HepG2	liver:	n/a	n/a
16	CEBPB	chr11:76650284-76650440	A549	lung:	n/a	n/a
17	CEBPB	chr11:76649010-76649284	MCF-7	breast:	n/a	chr11:76649114-76649125
18	CEBPB	chr11:76661504-76661691	IMR90	lung:	n/a	chr11:76661561-76661572
19	CEBPB	chr11:76661695-76661696	A549	lung:	n/a	n/a
20	CEBPB	chr11:76638313-76638502	Hela-S3	cervix:	n/a	chr11:76638421-76638432
21	CEBPB	chr11:76638242-76638548	IMR90	lung:	n/a	chr11:76638421-76638432
22	CEBPB	chr11:76638251-76638567	HepG2	liver:	n/a	chr11:76638421-76638432
23	CEBPD	chr11:76673965-76674262	HepG2	liver:	n/a	n/a
24	CHD1	chr11:76681188-76681323	GM12878	blood:	n/a	n/a
25	CTCF	chr11:76657414-76657425	ProgFib	skin:	n/a	n/a
26	CTCF	chr11:76685351-76685417	Hela-S3	cervix:	n/a	n/a
27	CTCF	chr11:76685289-76685392	MCF-7	breast:	n/a	n/a
28	CTCF	chr11:76656700-76656850	HBMEC	blood vessel:	n/a	n/a
29	CTCF	chr11:76684499-76684553	Fibrobl	skin:	n/a	n/a
30	CTCF	chr11:76657492-76657565	MCF-7	breast:	n/a	n/a
31	CTCF	chr11:76685460-76685610	HMEC	breast:	n/a	n/a
32	CTCF	chr11:76645562-76645624	GM10266	blood:	n/a	n/a
33	CTCF	chr11:76643960-76644110	HPAF	blood vessel:	n/a	n/a
34	CTCF	chr11:76685322-76685471	Pancreas_OC	pancreas:	n/a	n/a
35	CTCF	chr11:76671860-76672010	Caco-2	colon:	n/a	n/a
36	CTCF	chr11:76683700-76683850	HepG2	liver:	n/a	chr11:76683828-76683838
37	CUX1	chr11:76646432-76646447	K562	blood:	n/a	n/a
38	E2F4	chr11:76685046-76685172	MCF10A-Er-Src	breast:	n/a	n/a
39	E2F4	chr11:76682707-76682759	MCF10A-Er-Src	breast:	n/a	n/a
40	ELF1	chr11:76674055-76674370	HepG2	liver:	n/a	n/a
41	ELF1	chr11:76695803-76696213	MCF-7	breast:	n/a	n/a
42	ELF1	chr11:76673960-76674413	HepG2	liver:	n/a	n/a
43	EP300	chr11:76673850-76674482	HepG2	liver:	n/a	n/a
44	EP300	chr11:76673899-76674555	HepG2	liver:	n/a	n/a
45	EP300	chr11:76657728-76659309	SK-N-SH	brain:	n/a	chr11:76658990-76658999 chr11:76658989-76659003
46	EP300	chr11:76698234-76698549	K562	blood:	n/a	n/a
47	EP300	chr11:76674113-76674347	GM12878	blood:	n/a	n/a
48	EP300	chr11:76674084-76674415	HepG2	liver:	n/a	n/a
49	EP300	chr11:76658337-76658609	SK-N-SH_RA	brain:	n/a	n/a
50	EP300	chr11:76650230-76650490	HepG2	liver:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:76652096-76652146	NHBE	bronchial:	n/a
2	chr11:76644975-76645025	Jurkat	blood:	n/a
3	chr11:76709256-76709306	PrEC	prostate:	n/a
4	chr11:76652096-76652146	AG10803	skin:	n/a
5	chr11:76652096-76652146	HNPCEpiC	eye:	n/a
6	chr11:76644975-76645025	HMEC	breast:	n/a
7	chr11:76709256-76709306	BJ	skin:	n/a
8	chr11:76644975-76645025	NHDF-neo	bronchial:	n/a
9	chr11:76709256-76709306	Jurkat	blood:	n/a
10	chr11:76709256-76709306	HCF	heart:	n/a
11	chr11:76709256-76709306	HPAEpiC	pulmonary alveolar:	n/a
12	chr11:76709256-76709306	AoSMC	blood vessel:	n/a
13	chr11:76644975-76645025	NHBE	bronchial:	n/a
14	chr11:76644975-76645025	NH-A	brain:	n/a
15	chr11:76644975-76645025	AG09309	skin:	n/a
16	chr11:76644975-76645025	HCT-116	colon:	n/a
17	chr11:76709256-76709306	AG04450	lung:	fetal
18	chr11:76652096-76652146	HAEpiC	amniotic membrane:	n/a
19	chr11:76644975-76645025	K562	blood:	n/a
20	chr11:76652096-76652146	NB4	blood:	n/a
21	chr11:76644975-76645025	GM19239	blood:	n/a
22	chr11:76652096-76652146	ECC-1	luminal epithelium:	n/a
23	chr11:76644975-76645025	HAEpiC	amniotic membrane:	n/a
24	chr11:76644975-76645025	HIPEpiC	eye:	n/a
25	chr11:76644975-76645025	HCF	heart:	n/a
26	chr11:76652096-76652146	Caco-2	colon:	n/a
27	chr11:76709256-76709306	MCF-7	breast:	n/a
28	chr11:76644975-76645025	HNPCEpiC	eye:	n/a
29	chr11:76709256-76709306	NT2-D1	testis:	n/a
30	chr11:76644975-76645025	AG10803	skin:	n/a
31	chr11:76709256-76709306	IMR90	lung:	fetal
32	chr11:76652096-76652146	HEEpiC	esophagus:	n/a
33	chr11:76709256-76709306	Caco-2	colon:	n/a
34	chr11:76644975-76645025	GM12891	blood:	n/a
35	chr11:76644975-76645025	NT2-D1	testis:	n/a
36	chr11:76709256-76709306	NHDF-neo	bronchial:	n/a
37	chr11:76709256-76709306	HCT-116	colon:	n/a
38	chr11:76652096-76652146	ovcar-3	ovarian:	n/a
39	chr11:76644975-76645025	SK-N-MC	brain:	n/a
40	chr11:76644975-76645025	ECC-1	luminal epithelium:	n/a
41	chr11:76652096-76652146	MCF-7	breast:	n/a
42	chr11:76644975-76645025	HRPEpiC	eye:	n/a
43	chr11:76709256-76709306	AG10803	skin:	n/a
44	chr11:76709256-76709306	Hela-S3	cervix:	n/a
45	chr11:76644975-76645025	HRCEpiC	kidney:	n/a
46	chr11:76709256-76709306	HRE	kidney:	n/a
47	chr11:76709256-76709306	HIPEpiC	eye:	n/a
48	chr11:76652096-76652146	HRE	kidney:	n/a
49	chr11:76652096-76652146	GM19239	blood:	n/a
50	chr11:76652096-76652146	GM12878	blood:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:76693879..76696563-chr11:76699673..76701721,2	MCF-7	breast:
2	chr11:76699145..76701750-chr11:76703493..76705984,2	K562	blood:
3	chr11:76653898..76657828-chr11:76664691..76666325,3	K562	blood:
4	chr11:76684953..76685685-chr11:76756997..76757683,2	MCF-7	breast:
5	chr11:76686294..76687888-chr11:76690773..76692768,2	K562	blood:
6	chr11:76666896..76668570-chr11:76671083..76673989,2	K562	blood:
7	chr11:76653898..76657828-chr11:76664691..76666325,3	K562	blood:
8	chr11:76630803..76631497-chr11:76645979..76646483,2	MCF-7	breast:
9	chr11:76666896..76668570-chr11:76671083..76673989,2	K562	blood:
10	chr11:76631230..76632979-chr11:76654933..76656513,2	K562	blood:
11	chr11:76686294..76687888-chr11:76690773..76692768,2	K562	blood:
12	chr11:76691402..76695270-chr11:76696975..76699875,3	K562	blood:
13	chr11:76630886..76632771-chr11:76660350..76662030,2	K562	blood:
14	chr11:76693879..76696563-chr11:76699673..76701721,2	MCF-7	breast:
15	chr11:76691341..76694336-chr11:76696975..76699945,2	K562	blood:
16	chr11:76691341..76694336-chr11:76696975..76699945,2	K562	blood:
17	chr11:76684575..76686730-chr11:76722373..76724667,2	MCF-7	breast:
18	chr11:76691402..76695270-chr11:76696975..76699875,3	K562	blood:
19	chr11:76643902..76644760-chr11:76756381..76757685,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GDPD4-2	chr11:76689445-76689663	ENSG00000254988.1
2	lnc-GDPD4-2	chr11:76666461-76666629	ENSG00000254988.1
3	lnc-GDPD4-2	chr11:76669878-76670057	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: 2571 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:2571 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4379869	chr11:76637651-76637652	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs555155221	chr11:76637679-76637680	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs4479014	chr11:76637680-76637681	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs142469431	chr11:76637687-76637688	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs113648802	chr11:76637706-76637707	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs199519117	chr11:76637718-76637719	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs4604914	chr11:76637730-76637731	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs368827819	chr11:76637743-76637744	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs541929469	chr11:76637754-76637755	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs72945410	chr11:76637756-76637757	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs376964766	chr11:76637758-76637759	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs35276680	chr11:76637760-76637761	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs4457775	chr11:76637785-76637786	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs547265378	chr11:76637793-76637794	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs570457850	chr11:76637803-76637804	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs532361695	chr11:76637853-76637854	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs552250722	chr11:76637893-76637894	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs569239712	chr11:76637909-76637910	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs537926739	chr11:76637919-76637920	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs548681940	chr11:76637920-76637921	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs568654606	chr11:76637940-76637941	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs534423184	chr11:76637952-76637953	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs368097440	chr11:76637965-76637966	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs142432682	chr11:76637971-76637972	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs547762734	chr11:76637996-76637997	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs577571493	chr11:76638087-76638088	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs183755754	chr11:76638096-76638097	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs555857625	chr11:76638104-76638105	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs35650303	chr11:76638106-76638107	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs371821053	chr11:76638152-76638153	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs576004538	chr11:76638232-76638233	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs563110507	chr11:76638291-76638292	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs530546696	chr11:76638336-76638337	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs10793206	chr11:76638338-76638339	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs571129286	chr11:76638346-76638347	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs187583034	chr11:76638347-76638348	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs571904531	chr11:76638353-76638354	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs540866769	chr11:76638393-76638394	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs10899316	chr11:76638428-76638429	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs146645346	chr11:76638468-76638469	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs36050079	chr11:76638502-76638503	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs577660652	chr11:76638503-76638504	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs550074404	chr11:76638510-76638511	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs139152345	chr11:76638521-76638522	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs140525348	chr11:76638542-76638543	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs183021101	chr11:76638551-76638552	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs10793207	chr11:76638576-76638577	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs138306617	chr11:76638597-76638598	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs529780021	chr11:76638648-76638649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs375819921	chr11:76638652-76638653	Weak 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:964 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:76630200-76643400	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr11:76630200-76645600	Weak transcription	Fetal Brain Female	brain
3	chr11:76630600-76643200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr11:76631400-76643200	Weak transcription	Primary neutrophils fromperipheralblood	blood
5	chr11:76631400-76643400	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr11:76631400-76643600	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr11:76631400-76644600	Weak transcription	Small Intestine	intestine
8	chr11:76631400-76644800	Weak transcription	Fetal Muscle Trunk	muscle
9	chr11:76631400-76645000	Weak transcription	Fetal Stomach	stomach
10	chr11:76631400-76645600	Weak transcription	Esophagus	oesophagus
11	chr11:76631400-76645600	Weak transcription	Placenta	Placenta
12	chr11:76631400-76645600	Weak transcription	Stomach Smooth Muscle	stomach
13	chr11:76631400-76645800	Weak transcription	Fetal Lung	lung
14	chr11:76631400-76646000	Weak transcription	HUVEC	blood vessel
15	chr11:76631400-76649000	Weak transcription	Aorta	Aorta
16	chr11:76631400-76655000	Weak transcription	Primary B cells from cord blood	blood
17	chr11:76631400-76688400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr11:76631600-76643000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr11:76631600-76643000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr11:76631600-76643000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr11:76631600-76643000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr11:76631600-76643000	Weak transcription	Adipose Nuclei	Adipose
23	chr11:76631600-76643200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
24	chr11:76631600-76643200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr11:76631600-76643200	Weak transcription	Cortex derived primary cultured neurospheres	brain
26	chr11:76631600-76643200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr11:76631600-76643200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr11:76631600-76643200	Weak transcription	HMEC	breast
29	chr11:76631600-76643400	Weak transcription	Dnd41	blood
30	chr11:76631600-76643600	Weak transcription	A549	lung
31	chr11:76631600-76643600	Weak transcription	NHDF-Ad	bronchial
32	chr11:76631600-76643800	Weak transcription	NHEK	skin
33	chr11:76631600-76644800	Weak transcription	Primary T helper cells PMA-I stimulated	--
34	chr11:76631600-76645000	Weak transcription	Primary B cells from peripheral blood	blood
35	chr11:76631600-76645000	Weak transcription	Fetal Kidney	kidney
36	chr11:76631600-76645400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr11:76631600-76645600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
38	chr11:76631600-76645800	Weak transcription	Brain Anterior Caudate	brain
39	chr11:76631600-76645800	Weak transcription	Brain Inferior Temporal Lobe	brain
40	chr11:76631600-76645800	Weak transcription	Brain Substantia Nigra	brain
41	chr11:76631600-76646000	Weak transcription	Primary T cells from cord blood	blood
42	chr11:76631600-76646400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
43	chr11:76631600-76646600	Weak transcription	Primary T helper cells fromperipheralblood	blood
44	chr11:76631600-76646600	Weak transcription	Brain Cingulate Gyrus	brain
45	chr11:76631600-76657000	Weak transcription	Sigmoid Colon	Sigmoid Colon
46	chr11:76631600-76670200	Weak transcription	Left Ventricle	heart
47	chr11:76631600-76671600	Weak transcription	Ovary	ovary
48	chr11:76632000-76643800	Weak transcription	Liver	Liver
49	chr11:76632200-76645800	Weak transcription	Duodenum Mucosa	Duodenum
50	chr11:76633000-76643000	Weak transcription	Rectal Mucosa Donor 29	rectum

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