Variant report

Variant	nsv482156
Chromosome Location	chr11:3686817-3692614
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:57)
CpG islands
(count:488)
Chromatin interactive
region (count:5)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:57 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr11:3687100-3687250	K562	blood:	n/a	n/a
2	CTCF	chr11:3687019-3687356	K562	blood:	n/a	n/a
3	CTCF	chr11:3687108-3687263	K562	blood:	n/a	n/a
4	E2F6	chr11:3689094-3689512	H1-hESC	embryonic stem cell:	n/a	chr11:3689288-3689295 chr11:3689287-3689299 chr11:3689288-3689295 chr11:3689287-3689296 chr11:3689284-3689298 chr11:3689288-3689295
5	GATA3	chr11:3689170-3689322	SH-SY5Y	brain:	n/a	n/a
6	HMGN3	chr11:3687405-3687540	K562	blood:	n/a	n/a
7	JUND	chr11:3687174-3687255	K562	blood:	n/a	n/a
8	MAX	chr11:3686893-3687169	NB4	blood:	n/a	chr11:3687021-3687031
9	MAZ	chr11:3687075-3687202	K562	blood:	n/a	n/a
10	MAZ	chr11:3692230-3692414	HepG2	liver:	n/a	n/a
11	MYC	chr11:3687055-3687228	K562	blood:	n/a	n/a
12	POLR2A	chr11:3691874-3691964	H1-hESC	embryonic stem cell:	n/a	n/a
13	POLR2A	chr11:3691811-3692100	HepG2	liver:	n/a	n/a
14	POLR2A	chr11:3691626-3692244	K562	blood:	n/a	n/a
15	POLR2A	chr11:3689767-3694248	PANC-1	pancreas:	n/a	n/a
16	POLR2A	chr11:3691016-3691198	A549	lung:	n/a	n/a
17	POLR2A	chr11:3691717-3692402	SK-N-MC	brain:	n/a	n/a
18	POLR2A	chr11:3688895-3688999	HUVEC	blood vessel:	n/a	n/a
19	POLR2A	chr11:3691053-3691381	K562	blood:	n/a	n/a
20	POLR2A	chr11:3692034-3692086	Hela-S3	cervix:	n/a	n/a
21	POLR2A	chr11:3692552-3692850	HepG2	liver:	n/a	n/a
22	POLR2A	chr11:3691654-3693033	K562	blood:	n/a	n/a
23	POLR2A	chr11:3691718-3691954	K562	blood:	n/a	n/a
24	POLR2A	chr11:3687126-3687181	K562	blood:	n/a	n/a
25	POLR2A	chr11:3689048-3689080	HUVEC	blood vessel:	n/a	n/a
26	POLR2A	chr11:3690963-3694280	PFSK-1	brain:	n/a	n/a
27	POLR2A	chr11:3690808-3690814	K562	blood:	n/a	n/a
28	POLR2A	chr11:3692039-3692042	H1-hESC	embryonic stem cell:	n/a	n/a
29	POLR2A	chr11:3690442-3690652	K562	blood:	n/a	n/a
30	POLR2A	chr11:3691919-3691994	MCF-7	breast:	n/a	n/a
31	POLR2A	chr11:3691094-3691507	Hela-S3	cervix:	n/a	n/a
32	POLR2A	chr11:3692156-3692182	HepG2	liver:	n/a	n/a
33	POLR2A	chr11:3691967-3692035	H1-hESC	embryonic stem cell:	n/a	n/a
34	POLR2A	chr11:3692576-3692869	K562	blood:	n/a	n/a
35	POLR2A	chr11:3691384-3691404	K562	blood:	n/a	n/a
36	POLR2A	chr11:3690541-3690740	Hela-S3	cervix:	n/a	n/a
37	POLR2A	chr11:3690470-3692477	PANC-1	pancreas:	n/a	n/a
38	POLR2A	chr11:3692462-3692784	Hela-S3	cervix:	n/a	n/a
39	POLR2A	chr11:3686999-3687047	H1-hESC	embryonic stem cell:	n/a	n/a
40	POLR2A	chr11:3692376-3692437	HepG2	liver:	n/a	n/a
41	POLR2A	chr11:3692402-3692410	Hela-S3	cervix:	n/a	n/a
42	POLR2A	chr11:3691620-3691709	K562	blood:	n/a	n/a
43	POLR2A	chr11:3692238-3694154	Hela-S3	cervix:	n/a	n/a
44	POLR2A	chr11:3692195-3692249	HepG2	liver:	n/a	n/a
45	POLR2A	chr11:3692545-3693322	PANC-1	pancreas:	n/a	n/a
46	POLR2A	chr11:3688833-3688954	A549	lung:	n/a	n/a
47	POLR2A	chr11:3687737-3688255	SK-N-MC	brain:	n/a	n/a
48	POLR2A	chr11:3687044-3687125	K562	blood:	n/a	n/a
49	POLR2A	chr11:3691244-3691393	K562	blood:	n/a	n/a
50	POLR2A	chr11:3691069-3691156	HUVEC	blood vessel:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:3688526-3688576	HRCEpiC	kidney:	n/a
2	chr11:3689006-3689056	HL-60	blood:	n/a
3	chr11:3692187-3692237	PrEC	prostate:	n/a
4	chr11:3692562-3692612	NT2-D1	testis:	n/a
5	chr11:3692562-3692612	GM12891	blood:	n/a
6	chr11:3686892-3686942	HPAEpiC	pulmonary alveolar:	n/a
7	chr11:3690320-3690370	HCPEpiC	choroid plexus:	n/a
8	chr11:3688722-3688772	SK-N-SH_RA	brain:	n/a
9	chr11:3690320-3690370	HEK293	kidney:	embryo
10	chr11:3692562-3692612	ECC-1	luminal epithelium:	n/a
11	chr11:3688985-3689035	Caco-2	colon:	n/a
12	chr11:3688722-3688772	HCT-116	colon:	n/a
13	chr11:3690320-3690370	PFSK-1	brain:	n/a
14	chr11:3688985-3689035	GM12892	blood:	n/a
15	chr11:3692187-3692237	AG04450	lung:	fetal
16	chr11:3688526-3688576	AG09319	gingival:	n/a
17	chr11:3688526-3688576	PANC-1	pancreas:	n/a
18	chr11:3692187-3692237	ECC-1	luminal epithelium:	n/a
19	chr11:3689006-3689056	Caco-2	colon:	n/a
20	chr11:3690320-3690370	HRCEpiC	kidney:	n/a
21	chr11:3686892-3686942	NHBE	bronchial:	n/a
22	chr11:3688526-3688576	GM12878	blood:	n/a
23	chr11:3692562-3692612	HRCEpiC	kidney:	n/a
24	chr11:3688526-3688576	GM12891	blood:	n/a
25	chr11:3689006-3689056	HepG2	liver:	n/a
26	chr11:3688985-3689035	NH-A	brain:	n/a
27	chr11:3692562-3692612	RPTEC	kidney:	n/a
28	chr11:3688985-3689035	AoSMC	blood vessel:	n/a
29	chr11:3692187-3692237	HUVEC	blood vessel:	n/a
30	chr11:3688526-3688576	LNCaP	prostate:	n/a
31	chr11:3688985-3689035	MCF-7	breast:	n/a
32	chr11:3688722-3688772	SKMC	muscle:	n/a
33	chr11:3692187-3692237	SKMC	muscle:	n/a
34	chr11:3688722-3688772	GM06990	blood:	n/a
35	chr11:3688985-3689035	SAEC	small airway:	n/a
36	chr11:3692562-3692612	Jurkat	blood:	n/a
37	chr11:3688722-3688772	CMK	blood:	n/a
38	chr11:3689006-3689056	BJ	skin:	n/a
39	chr11:3692187-3692237	AG09309	skin:	n/a
40	chr11:3692562-3692612	GM12878	blood:	n/a
41	chr11:3688526-3688576	RPTEC	kidney:	n/a
42	chr11:3690320-3690370	HUVEC	blood vessel:	n/a
43	chr11:3689006-3689056	SK-N-SH	brain:	n/a
44	chr11:3688985-3689035	HRPEpiC	eye:	n/a
45	chr11:3690320-3690370	NB4	blood:	n/a
46	chr11:3688985-3689035	PANC-1	pancreas:	n/a
47	chr11:3688985-3689035	IMR90	lung:	fetal
48	chr11:3688985-3689035	ECC-1	luminal epithelium:	n/a
49	chr11:3692187-3692237	HAEpiC	amniotic membrane:	n/a
50	chr11:3688526-3688576	HNPCEpiC	eye:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:3690214..3692780-chr11:3696076..3698742,2	MCF-7	breast:
2	chr11:3679748..3681336-chr11:3687439..3689154,2	K562	blood:
3	chr11:3692345..3692867-chr15:44084030..44084743,2	NB4	blood:
4	chr11:3692006..3695264-chr11:3695478..3698452,4	K562	blood:
5	chr11:3690371..3694787-chr11:3695669..3699766,6	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NUP98-1	chr11:3690964-3691117	NONHSAT017612
2	lnc-NUP98-1	chr11:3689730-3690580	NONHSAT017612

No data

Variant related genes	Relation type
ENSG00000201279	TF binding region
CHRNA10	TF binding region
ENSG00000200201	TF binding region
ENSG00000201279	CpG island
CHRNA10	CpG island
ENSG00000200201	CpG island
ENSG00000140264	chromatin interactions
ENSG00000110713	chromatin interactions

Extended variants
information (count: 329 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:329 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs548874500	chr11:3686835-3686836	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs55693185	chr11:3686859-3686860	Weak transcription Strong transcription	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs572675582	chr11:3686862-3686863	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs543198232	chr11:3686903-3686904	Weak transcription Strong transcription	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
5	rs368126517	chr11:3686912-3686913	Weak transcription Strong transcription	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
6	rs12221525	chr11:3686944-3686945	Weak transcription Strong transcription	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs76587710	chr11:3686957-3686958	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs543472276	chr11:3687025-3687026	Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs111348374	chr11:3687048-3687049	Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs55798582	chr11:3687049-3687050	Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs149459290	chr11:3687096-3687097	Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs143897402	chr11:3687104-3687105	Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs74049384	chr11:3687113-3687114	Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs548726633	chr11:3687117-3687118	Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
15	rs571785236	chr11:3687128-3687129	Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
16	rs114978383	chr11:3687166-3687167	Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
17	rs112933780	chr11:3687171-3687172	Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
18	rs537925315	chr11:3687252-3687253	Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
19	rs549547097	chr11:3687254-3687255	Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
20	rs571213637	chr11:3687295-3687296	Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
21	rs113881064	chr11:3687318-3687319	Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
22	rs151092008	chr11:3687343-3687344	Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
23	rs539012366	chr11:3687346-3687347	Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
24	rs554510167	chr11:3687388-3687389	Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
25	rs377727660	chr11:3687390-3687391	Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
26	rs370972331	chr11:3687419-3687420	Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
27	rs536855924	chr11:3687428-3687429	Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
28	rs2231548	chr11:3687429-3687430	Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
29	rs116632003	chr11:3687449-3687450	Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
30	rs543881167	chr11:3687450-3687451	Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
31	rs368359091	chr11:3687467-3687468	Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
32	rs146888913	chr11:3687470-3687471	Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
33	rs140488178	chr11:3687471-3687472	Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
34	rs55650071	chr11:3687474-3687475	Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
35	rs56054950	chr11:3687476-3687477	Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
36	rs201776567	chr11:3687479-3687480	Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
37	rs138310150	chr11:3687495-3687496	Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
38	rs149591762	chr11:3687496-3687497	Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
39	rs143107810	chr11:3687504-3687505	Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
40	rs563196190	chr11:3687510-3687511	Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
41	rs376322912	chr11:3687514-3687515	Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
42	rs367930797	chr11:3687518-3687519	Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
43	rs148252978	chr11:3687530-3687531	Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
44	rs188340188	chr11:3687531-3687532	Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
45	rs371388495	chr11:3687538-3687539	Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
46	rs201083934	chr11:3687550-3687551	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs141309069	chr11:3687551-3687552	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs571209251	chr11:3687553-3687554	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs200226257	chr11:3687624-3687625	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs2231547	chr11:3687626-3687627	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	19432969	CNVD
Alzheimer''s disease	17576883	CNVD
Long-qt syndrome	17576883	CNVD
Emphysema	19352772	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chordoma	18071362	CNVD
Breast cancer	16608533	CNVD
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
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
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Neuroblastoma	21124317	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Schizophrenia	21399695	CNVD
Gastric cancer	16891809	CNVD
Cancer	17160897	CNVD
Multiple myeloma	16616336	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Cancer	17440070	CNVD

Chromatin state (count:262 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:3673000-3687200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr11:3680200-3689400	Strong transcription	Skeletal Muscle Female	skeletal muscle
3	chr11:3681000-3687800	Weak transcription	A549	lung
4	chr11:3681400-3691200	Strong transcription	Skeletal Muscle Male	skeletal muscle
5	chr11:3681800-3693200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr11:3682400-3697200	Weak transcription	Fetal Brain Male	brain
7	chr11:3682800-3688400	Weak transcription	Small Intestine	intestine
8	chr11:3683000-3696600	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr11:3683200-3687200	Weak transcription	HSMM	muscle
10	chr11:3683200-3694000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr11:3683400-3687000	Weak transcription	Dnd41	blood
12	chr11:3683400-3687200	Weak transcription	HSMMtube	muscle
13	chr11:3683400-3690200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr11:3683600-3691400	Weak transcription	NH-A	brain
15	chr11:3683600-3693400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
16	chr11:3683600-3693400	Weak transcription	NHDF-Ad	bronchial
17	chr11:3683800-3687000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr11:3683800-3687000	Weak transcription	Brain Inferior Temporal Lobe	brain
19	chr11:3683800-3687600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
20	chr11:3684000-3687200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
21	chr11:3684000-3687600	Weak transcription	HUES64 Cell Line	embryonic stem cell
22	chr11:3684000-3687600	Weak transcription	Primary T cells fromperipheralblood	blood
23	chr11:3684200-3687200	Weak transcription	Colon Smooth Muscle	Colon
24	chr11:3684400-3705400	Strong transcription	Fetal Muscle Leg	muscle
25	chr11:3684800-3688800	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr11:3685000-3687000	Strong transcription	Muscle Satellite Cultured Cells	--
27	chr11:3685000-3688800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr11:3685000-3690400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
29	chr11:3685000-3693200	Weak transcription	Hela-S3	cervix
30	chr11:3685000-3728000	Strong transcription	Stomach Smooth Muscle	stomach
31	chr11:3685000-3743800	Strong transcription	Duodenum Mucosa	Duodenum
32	chr11:3685200-3687000	Weak transcription	Liver	Liver
33	chr11:3685200-3687400	Weak transcription	HUES48 Cell Line	embryonic stem cell
34	chr11:3685200-3689600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
35	chr11:3685200-3689600	Strong transcription	Fetal Stomach	stomach
36	chr11:3685200-3690200	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr11:3685200-3690400	Strong transcription	Lung	lung
38	chr11:3685200-3691800	Strong transcription	Ovary	ovary
39	chr11:3685200-3693200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr11:3685200-3695400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr11:3685200-3702600	Strong transcription	Fetal Intestine Small	intestine
42	chr11:3685200-3705600	Strong transcription	Brain Germinal Matrix	brain
43	chr11:3685200-3728200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr11:3685200-3728200	Strong transcription	Thymus	Thymus
45	chr11:3685200-3730000	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
46	chr11:3685200-3766800	Strong transcription	Placenta	Placenta
47	chr11:3685400-3688200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr11:3685400-3688400	Strong transcription	NHEK	skin
49	chr11:3685400-3688400	Strong transcription	Osteobl	bone
50	chr11:3685400-3689800	Weak transcription	Brain Substantia Nigra	brain

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