Variant report

Variant	nsv511473
Chromosome Location	chr11:34202953-34212883
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:38)
CpG islands
(count:61)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:38 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr11:34212014-34212274	GM12878	blood:	n/a	n/a
2	CHD1	chr11:34207099-34207121	GM12878	blood:	n/a	n/a
3	CTBP2	chr11:34207727-34208577	H1-hESC	embryonic stem cell:	n/a	n/a
4	CTCF	chr11:34204120-34204270	AG10803	skin:	n/a	n/a
5	CTCF	chr11:34208440-34208590	GM12873	blood:	n/a	n/a
6	CTCF	chr11:34211880-34212030	GM06990	blood:	n/a	n/a
7	CTCF	chr11:34204945-34204988	GM20000	blood:	n/a	n/a
8	CTCF	chr11:34211880-34212030	GM12872	blood:	n/a	n/a
9	EBF1	chr11:34204024-34204309	GM12878	blood:	n/a	chr11:34204188-34204199
10	EBF1	chr11:34203979-34204338	GM12878	blood:	n/a	chr11:34204188-34204199
11	EBF1	chr11:34203994-34204440	GM12878	blood:	n/a	chr11:34204188-34204199
12	FOXP2	chr11:34208172-34208363	PFSK-1	brain:	n/a	n/a
13	MAX	chr11:34206223-34206463	K562	blood:	n/a	chr11:34206365-34206374 chr11:34206365-34206375
14	MAX	chr11:34206283-34206514	NB4	blood:	n/a	chr11:34206365-34206374 chr11:34206365-34206375
15	MAX	chr11:34209790-34210030	H1-hESC	embryonic stem cell:	n/a	n/a
16	NFIC	chr11:34212004-34212456	GM12878	blood:	n/a	n/a
17	POLR2A	chr11:34204821-34204861	HepG2	liver:	n/a	n/a
18	POLR2A	chr11:34207840-34208041	H1-hESC	embryonic stem cell:	n/a	n/a
19	POLR2A	chr11:34204884-34204897	HepG2	liver:	n/a	n/a
20	POLR2A	chr11:34208261-34208267	H1-hESC	embryonic stem cell:	n/a	n/a
21	POLR2A	chr11:34210644-34210667	MCF10A-Er-Src	breast:	n/a	n/a
22	POLR2A	chr11:34208248-34208258	H1-hESC	embryonic stem cell:	n/a	n/a
23	POLR2A	chr11:34208141-34208155	H1-hESC	embryonic stem cell:	n/a	n/a
24	POLR2A	chr11:34210436-34210642	H1-hESC	embryonic stem cell:	n/a	n/a
25	POLR2A	chr11:34208183-34208219	H1-hESC	embryonic stem cell:	n/a	n/a
26	POLR2A	chr11:34204793-34204815	HepG2	liver:	n/a	n/a
27	REST	chr11:34207483-34208468	H1-neurons	neurons:	n/a	n/a
28	REST	chr11:34207976-34208370	PFSK-1	brain:	n/a	n/a
29	RUNX3	chr11:34211984-34212390	GM12878	blood:	n/a	n/a
30	RUNX3	chr11:34211905-34212473	GM12878	blood:	n/a	n/a
31	SIN3A	chr11:34207811-34208337	H1-hESC	embryonic stem cell:	n/a	n/a
32	TBP	chr11:34207985-34208411	H1-hESC	embryonic stem cell:	n/a	n/a
33	TEAD4	chr11:34209709-34210137	H1-hESC	embryonic stem cell:	n/a	n/a
34	TEAD4	chr11:34209758-34210112	H1-hESC	embryonic stem cell:	n/a	n/a
35	USF2	chr11:34207077-34207238	GM12878	blood:	n/a	n/a
36	WRNIP1	chr11:34204474-34204590	GM12878	blood:	n/a	n/a
37	YY1	chr11:34209611-34210100	H1-hESC	embryonic stem cell:	n/a	n/a
38	ZNF384	chr11:34208936-34209136	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:34208754-34208804	K562	blood:	n/a
2	chr11:34208754-34208804	GM12891	blood:	n/a
3	chr11:34208754-34208804	HCPEpiC	choroid plexus:	n/a
4	chr11:34208754-34208804	HPAEpiC	pulmonary alveolar:	n/a
5	chr11:34208754-34208804	NB4	blood:	n/a
6	chr11:34208754-34208804	AG09309	skin:	n/a
7	chr11:34208754-34208804	AG04449	skin:	fetal
8	chr11:34208754-34208804	T-47D	breast:	n/a
9	chr11:34208754-34208804	BJ	skin:	n/a
10	chr11:34208754-34208804	HepG2	liver:	n/a
11	chr11:34208754-34208804	SKMC	muscle:	n/a
12	chr11:34208754-34208804	HIPEpiC	eye:	n/a
13	chr11:34208754-34208804	Caco-2	colon:	n/a
14	chr11:34208754-34208804	PANC-1	pancreas:	n/a
15	chr11:34208754-34208804	HRPEpiC	eye:	n/a
16	chr11:34208754-34208804	IMR90	lung:	fetal
17	chr11:34208754-34208804	HCM	heart:	n/a
18	chr11:34208754-34208804	SAEC	small airway:	n/a
19	chr11:34208754-34208804	MCF-7	breast:	n/a
20	chr11:34208754-34208804	SK-N-SH	brain:	n/a
21	chr11:34208754-34208804	PrEC	prostate:	n/a
22	chr11:34208754-34208804	ovcar-3	ovarian:	n/a
23	chr11:34208754-34208804	GM12892	blood:	n/a
24	chr11:34208754-34208804	HNPCEpiC	eye:	n/a
25	chr11:34208754-34208804	U87	brain:	n/a
26	chr11:34208754-34208804	HRCEpiC	kidney:	n/a
27	chr11:34208754-34208804	HUVEC	blood vessel:	n/a
28	chr11:34208754-34208804	AG09319	gingival:	n/a
29	chr11:34208754-34208804	MCF10A-Er-Src	breast:	n/a
30	chr11:34208754-34208804	Hela-S3	cervix:	n/a
31	chr11:34208754-34208804	AG10803	skin:	n/a
32	chr11:34208754-34208804	GM12878	blood:	n/a
33	chr11:34208754-34208804	HMEC	breast:	n/a
34	chr11:34208754-34208804	RPTEC	kidney:	n/a
35	chr11:34208754-34208804	BE2_C	brain:	n/a
36	chr11:34208754-34208804	ProgFib	skin:	n/a
37	chr11:34208754-34208804	NT2-D1	testis:	n/a
38	chr11:34208754-34208804	NHDF-neo	bronchial:	n/a
39	chr11:34208754-34208804	Jurkat	blood:	n/a
40	chr11:34208754-34208804	CMK	blood:	n/a
41	chr11:34208754-34208804	SK-N-SH_RA	brain:	n/a
42	chr11:34208754-34208804	HCT-116	colon:	n/a
43	chr11:34208754-34208804	LNCaP	prostate:	n/a
44	chr11:34208754-34208804	H1-hESC	embryonic stem cell:	embryo
45	chr11:34208754-34208804	SK-N-MC	brain:	n/a
46	chr11:34208754-34208804	Hepatocyte	liver:	n/a
47	chr11:34208754-34208804	GM19239	blood:	n/a
48	chr11:34208754-34208804	GM06990	blood:	n/a
49	chr11:34208754-34208804	PFSK-1	brain:	n/a
50	chr11:34208754-34208804	AG04450	lung:	fetal

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:34206532..34209064-chr11:34210711..34213198,2	K562	blood:
2	chr11:34198458..34205212-chr11:34376041..34381079,14	MCF-7	breast:
3	chr11:34202988..34205235-chr11:34209660..34212363,2	K562	blood:
4	chr11:34200978..34204921-chr11:34206145..34211160,6	K562	blood:
5	chr11:34194502..34196652-chr11:34202672..34204738,2	MCF-7	breast:
6	chr11:34201889..34204263-chr11:34210189..34212019,2	MCF-7	breast:
7	chr11:34211397..34213472-chr11:34217305..34219861,2	K562	blood:
8	chr11:34211972..34213946-chr11:34215834..34218805,2	K562	blood:
9	chr11:34209674..34212372-chr11:34378433..34380265,3	MCF-7	breast:
10	chr11:34210356..34212606-chr11:34378528..34380428,2	MCF-7	breast:
11	chr11:34199620..34202889-chr11:34205068..34208989,4	K562	blood:

No data

Variant related genes	Relation type
ENSG00000201867	TF binding region
ENSG00000201867	CpG island
ENSG00000201867	chromatin interactions
ENSG00000166016	chromatin interactions

Extended variants
information (count: 397 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:397 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2467377	chr11:34202953-34202954	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs539656804	chr11:34202963-34202964	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs550332794	chr11:34203015-34203016	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs553219209	chr11:34203021-34203022	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs34427038	chr11:34203034-34203035	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs116658841	chr11:34203055-34203056	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs555714585	chr11:34203076-34203077	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs575588097	chr11:34203080-34203081	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs2467376	chr11:34203208-34203209	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs564574271	chr11:34203223-34203224	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs73507415	chr11:34203231-34203232	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs546036007	chr11:34203253-34203254	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs369380366	chr11:34203267-34203268	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs559356532	chr11:34203272-34203273	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs111765912	chr11:34203305-34203306	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs548228568	chr11:34203348-34203349	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs55687647	chr11:34203390-34203391	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs76981800	chr11:34203523-34203524	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs550223309	chr11:34203525-34203526	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs570230802	chr11:34203585-34203586	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs534933886	chr11:34203586-34203587	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs143038557	chr11:34203629-34203630	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs539617635	chr11:34203636-34203637	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs113920024	chr11:34203638-34203639	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs376722641	chr11:34203673-34203674	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs566985601	chr11:34203686-34203687	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs536134588	chr11:34203731-34203732	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs555829730	chr11:34203732-34203733	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs571884910	chr11:34203784-34203785	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs544626268	chr11:34203813-34203814	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs61880413	chr11:34203841-34203842	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs2143868	chr11:34203862-34203863	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs578157947	chr11:34203883-34203884	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs182626988	chr11:34203937-34203938	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs559491592	chr11:34203971-34203972	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs145181364	chr11:34203978-34203979	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs542061904	chr11:34204048-34204049	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs6484699	chr11:34204049-34204050	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs536696510	chr11:34204051-34204052	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs117989378	chr11:34204053-34204054	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs550186251	chr11:34204054-34204055	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs373061696	chr11:34204057-34204058	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs563768988	chr11:34204058-34204059	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs573064100	chr11:34204064-34204065	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs546416075	chr11:34204069-34204070	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs370710638	chr11:34204086-34204087	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs187776147	chr11:34204100-34204101	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs193243103	chr11:34204101-34204102	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs2473913	chr11:34204128-34204129	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs569466284	chr11:34204172-34204173	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	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:389 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:34192800-34203000	Weak transcription	Aorta	Aorta
2	chr11:34196200-34207600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr11:34196400-34203400	Weak transcription	Fetal Brain Male	brain
4	chr11:34196400-34206800	Weak transcription	Gastric	stomach
5	chr11:34196400-34207600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr11:34196600-34203000	Weak transcription	Skeletal Muscle Female	skeletal muscle
7	chr11:34196600-34204400	Weak transcription	HSMM	muscle
8	chr11:34196600-34204800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr11:34196600-34205800	Weak transcription	Fetal Brain Female	brain
10	chr11:34196600-34206000	Weak transcription	Pancreas	Pancrea
11	chr11:34196600-34206200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr11:34196600-34207600	Weak transcription	Left Ventricle	heart
13	chr11:34196600-34210200	Weak transcription	HepG2	liver
14	chr11:34196600-34214000	Weak transcription	Stomach Mucosa	stomach
15	chr11:34196800-34203200	Weak transcription	Stomach Smooth Muscle	stomach
16	chr11:34196800-34205000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr11:34196800-34206800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr11:34197000-34207400	Weak transcription	HSMMtube	muscle
19	chr11:34197400-34203600	Weak transcription	Right Ventricle	heart
20	chr11:34197400-34204400	Enhancers	GM12878-XiMat	blood
21	chr11:34197400-34205000	Weak transcription	Liver	Liver
22	chr11:34197800-34205200	Enhancers	Brain Hippocampus Middle	brain
23	chr11:34198000-34203800	Enhancers	Brain Cingulate Gyrus	brain
24	chr11:34198000-34204000	Enhancers	Brain Anterior Caudate	brain
25	chr11:34198000-34204000	Enhancers	Brain Substantia Nigra	brain
26	chr11:34198600-34207000	Weak transcription	NHEK	skin
27	chr11:34198800-34207000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr11:34199200-34209800	Weak transcription	A549	lung
29	chr11:34199600-34206600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr11:34199800-34206000	Weak transcription	Brain Germinal Matrix	brain
31	chr11:34200800-34203200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr11:34200800-34203400	Enhancers	Cortex derived primary cultured neurospheres	brain
33	chr11:34200800-34203400	Enhancers	Fetal Stomach	stomach
34	chr11:34200800-34203600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
35	chr11:34201000-34203000	Weak transcription	Fetal Muscle Leg	muscle
36	chr11:34201000-34204000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr11:34201600-34203000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
38	chr11:34201800-34203600	Enhancers	Primary monocytes fromperipheralblood	blood
39	chr11:34201800-34203600	Enhancers	Placenta	Placenta
40	chr11:34201800-34203800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr11:34201800-34203800	Enhancers	Brain Inferior Temporal Lobe	brain
42	chr11:34202000-34203000	Weak transcription	Brain Angular Gyrus	brain
43	chr11:34202000-34203000	Weak transcription	Fetal Muscle Trunk	muscle
44	chr11:34202000-34203600	Enhancers	Monocytes-CD14+_RO01746	blood
45	chr11:34202000-34205200	Weak transcription	Fetal Kidney	kidney
46	chr11:34202200-34203200	Enhancers	Primary hematopoietic stem cells short term culture	blood
47	chr11:34202200-34207200	Weak transcription	HMEC	breast
48	chr11:34202400-34203200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
49	chr11:34202400-34207400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr11:34202400-34207400	Weak transcription	Fetal Lung	lung

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