Variant report

Variant	nsv7691
Chromosome Location	chr11:17151593-17196894
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:241)
CpG islands
(count:305)
Chromatin interactive
region (count:28)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:241 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:17166930-17166978	HepG2	liver:	n/a	n/a
2	ATF2	chr11:17175863-17176292	GM12878	blood:	n/a	n/a
3	BACH1	chr11:17174185-17174187	K562	blood:	n/a	n/a
4	BATF	chr11:17176430-17176573	GM12878	blood:	n/a	n/a
5	BATF	chr11:17176359-17176590	GM12878	blood:	n/a	n/a
6	BHLHE40	chr11:17175832-17176290	GM12878	blood:	n/a	n/a
7	BHLHE40	chr11:17167300-17167321	GM12878	blood:	n/a	n/a
8	CCNT2	chr11:17175986-17176208	K562	blood:	n/a	n/a
9	CEBPB	chr11:17192994-17193224	A549	lung:	n/a	chr11:17193126-17193137 chr11:17193126-17193137 chr11:17193126-17193139
10	CEBPB	chr11:17192984-17193350	ECC-1	luminal epithelium:	n/a	chr11:17193126-17193137 chr11:17193126-17193137 chr11:17193126-17193139
11	CEBPB	chr11:17186540-17186761	HepG2	liver:	n/a	n/a
12	CEBPB	chr11:17192948-17193324	IMR90	lung:	n/a	chr11:17193126-17193137 chr11:17193126-17193137 chr11:17193126-17193139
13	CEBPB	chr11:17186467-17186811	IMR90	lung:	n/a	n/a
14	CEBPB	chr11:17192929-17193332	Hela-S3	cervix:	n/a	chr11:17193126-17193137 chr11:17193126-17193137 chr11:17193126-17193139
15	CEBPB	chr11:17186438-17186841	K562	blood:	n/a	n/a
16	CEBPB	chr11:17186323-17186841	K562	blood:	n/a	n/a
17	CEBPB	chr11:17186448-17186825	HepG2	liver:	n/a	n/a
18	CEBPB	chr11:17192974-17193257	H1-hESC	embryonic stem cell:	n/a	chr11:17193126-17193137 chr11:17193126-17193137 chr11:17193126-17193139
19	CEBPB	chr11:17186455-17186834	ECC-1	luminal epithelium:	n/a	n/a
20	CEBPB	chr11:17192979-17193298	ECC-1	luminal epithelium:	n/a	chr11:17193126-17193137 chr11:17193126-17193137 chr11:17193126-17193139
21	CEBPB	chr11:17186464-17186803	HepG2	liver:	n/a	n/a
22	CEBPB	chr11:17186378-17186831	A549	lung:	n/a	n/a
23	CEBPB	chr11:17186469-17186760	K562	blood:	n/a	n/a
24	CEBPB	chr11:17192881-17193360	A549	lung:	n/a	chr11:17193126-17193137 chr11:17193126-17193137 chr11:17193126-17193139
25	CEBPB	chr11:17186378-17186905	MCF-7	breast:	n/a	n/a
26	CEBPB	chr11:17186418-17186868	MCF-7	breast:	n/a	n/a
27	CEBPB	chr11:17167446-17167491	A549	lung:	n/a	n/a
28	CEBPB	chr11:17186462-17186801	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr11:17186307-17186966	HCT-116	colon:	n/a	n/a
30	CEBPB	chr11:17186391-17186837	A549	lung:	n/a	n/a
31	CEBPB	chr11:17186480-17186720	HepG2	liver:	n/a	n/a
32	CEBPB	chr11:17186310-17186847	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr11:17186412-17186805	ECC-1	luminal epithelium:	n/a	n/a
34	CEBPB	chr11:17186449-17186801	A549	lung:	n/a	n/a
35	CEBPD	chr11:17186466-17186726	HepG2	liver:	n/a	n/a
36	CTCF	chr11:17154760-17154910	HepG2	liver:	n/a	n/a
37	CTCF	chr11:17174788-17174866	GM20000	blood:	n/a	n/a
38	CTCF	chr11:17183779-17183824	GM10248	blood:	n/a	n/a
39	CTCF	chr11:17176180-17176330	AG10803	skin:	n/a	n/a
40	CUX1	chr11:17175592-17175730	K562	blood:	n/a	n/a
41	CUX1	chr11:17185497-17185546	K562	blood:	n/a	n/a
42	CUX1	chr11:17186009-17186375	K562	blood:	n/a	chr11:17186144-17186153
43	E2F4	chr11:17151561-17151980	MCF10A-Er-Src	breast:	n/a	n/a
44	EBF1	chr11:17176079-17176290	GM12878	blood:	n/a	n/a
45	ELF1	chr11:17186446-17186701	K562	blood:	n/a	n/a
46	ELK1	chr11:17186443-17186774	Hela-S3	cervix:	n/a	n/a
47	ELK4	chr11:17186461-17186696	Hela-S3	cervix:	n/a	chr11:17186620-17186631
48	EP300	chr11:17156927-17156964	K562	blood:	n/a	n/a
49	EP300	chr11:17175970-17176445	GM12878	blood:	n/a	chr11:17176121-17176135
50	EP300	chr11:17175886-17176196	GM12878	blood:	n/a	chr11:17176121-17176135

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:17191617-17191667	PANC-1	pancreas:	n/a
2	chr11:17191235-17191285	HAEpiC	amniotic membrane:	n/a
3	chr11:17191235-17191285	SK-N-MC	brain:	n/a
4	chr11:17191617-17191667	SK-N-SH	brain:	n/a
5	chr11:17193765-17193815	AG09309	skin:	n/a
6	chr11:17191235-17191285	AG09319	gingival:	n/a
7	chr11:17191235-17191285	ProgFib	skin:	n/a
8	chr11:17193765-17193815	NH-A	brain:	n/a
9	chr11:17192372-17192422	ECC-1	luminal epithelium:	n/a
10	chr11:17191235-17191285	SKMC	muscle:	n/a
11	chr11:17191617-17191667	H1-hESC	embryonic stem cell:	embryo
12	chr11:17193765-17193815	HepG2	liver:	n/a
13	chr11:17191235-17191285	AG04450	lung:	fetal
14	chr11:17191235-17191285	AG09309	skin:	n/a
15	chr11:17191235-17191285	HUVEC	blood vessel:	n/a
16	chr11:17158572-17158622	HMEC	breast:	n/a
17	chr11:17193765-17193815	MCF10A-Er-Src	breast:	n/a
18	chr11:17192372-17192422	HCF	heart:	n/a
19	chr11:17191617-17191667	HAEpiC	amniotic membrane:	n/a
20	chr11:17158572-17158622	AG10803	skin:	n/a
21	chr11:17191235-17191285	NHBE	bronchial:	n/a
22	chr11:17158572-17158622	A549	lung:	n/a
23	chr11:17193765-17193815	HEEpiC	esophagus:	n/a
24	chr11:17192372-17192422	AG09319	gingival:	n/a
25	chr11:17158572-17158622	ovcar-3	ovarian:	n/a
26	chr11:17158572-17158622	HNPCEpiC	eye:	n/a
27	chr11:17158572-17158622	Caco-2	colon:	n/a
28	chr11:17158572-17158622	ECC-1	luminal epithelium:	n/a
29	chr11:17191235-17191285	Hela-S3	cervix:	n/a
30	chr11:17192372-17192422	AoSMC	blood vessel:	n/a
31	chr11:17192372-17192422	PANC-1	pancreas:	n/a
32	chr11:17191617-17191667	NH-A	brain:	n/a
33	chr11:17191235-17191285	U87	brain:	n/a
34	chr11:17192372-17192422	T-47D	breast:	n/a
35	chr11:17192372-17192422	LNCaP	prostate:	n/a
36	chr11:17192372-17192422	MCF10A-Er-Src	breast:	n/a
37	chr11:17191617-17191667	SK-N-SH_RA	brain:	n/a
38	chr11:17192372-17192422	SK-N-SH	brain:	n/a
39	chr11:17191617-17191667	Hela-S3	cervix:	n/a
40	chr11:17191235-17191285	NT2-D1	testis:	n/a
41	chr11:17193765-17193815	HPAEpiC	pulmonary alveolar:	n/a
42	chr11:17192372-17192422	PrEC	prostate:	n/a
43	chr11:17192372-17192422	HUVEC	blood vessel:	n/a
44	chr11:17191235-17191285	AG10803	skin:	n/a
45	chr11:17193765-17193815	GM12892	blood:	n/a
46	chr11:17191235-17191285	PFSK-1	brain:	n/a
47	chr11:17158572-17158622	AG04450	lung:	fetal
48	chr11:17158572-17158622	U87	brain:	n/a
49	chr11:17193765-17193815	BJ	skin:	n/a
50	chr11:17158572-17158622	HRE	kidney:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:17183106..17184886-chr11:17186963..17189434,2	MCF-7	breast:
2	chr11:17098455..17101207-chr11:17153666..17155751,2	K562	blood:
3	chr11:17182736..17185668-chr11:17187012..17188861,2	K562	blood:
4	chr11:17190589..17193043-chr11:17228030..17230019,2	MCF-7	breast:
5	chr11:17168815..17170392-chr11:17175190..17177011,2	K562	blood:
6	chr11:17182055..17184280-chr11:17186207..17188512,3	K562	blood:
7	chr11:17154024..17158946-chr11:17185264..17188139,4	K562	blood:
8	chr11:17168815..17170392-chr11:17175190..17177011,2	K562	blood:
9	chr11:17168623..17170231-chr11:17178492..17180803,2	K562	blood:
10	chr11:17181778..17184549-chr11:17240618..17243052,2	K562	blood:
11	chr11:17165805..17167971-chr11:17170717..17172780,2	K562	blood:
12	chr11:17167469..17170392-chr11:17173847..17176690,3	K562	blood:
13	chr11:17172410..17175625-chr11:17176189..17178392,3	MCF-7	breast:
14	chr11:17193774..17196751-chr11:17204153..17207102,2	K562	blood:
15	chr11:17183106..17184886-chr11:17186963..17189434,2	MCF-7	breast:
16	chr11:17165805..17167971-chr11:17170717..17172780,2	K562	blood:
17	chr11:17190320..17193251-chr11:17194290..17196394,2	K562	blood:
18	chr11:17194253..17196723-chr11:17227181..17229874,2	MCF-7	breast:
19	chr11:17182055..17184280-chr11:17186207..17188512,3	K562	blood:
20	chr11:17186616..17189507-chr11:17190943..17193289,3	K562	blood:
21	chr11:17168623..17170231-chr11:17178492..17180803,2	K562	blood:
22	chr11:17172410..17175625-chr11:17176189..17178392,3	MCF-7	breast:
23	chr11:17182736..17185668-chr11:17187012..17188861,2	K562	blood:
24	chr11:17154024..17158946-chr11:17185264..17188139,4	K562	blood:
25	chr11:17196415..17198675-chr11:17200267..17202983,2	K562	blood:
26	chr11:17191444..17193638-chr17:59471300..59473152,2	MCF-7	breast:
27	chr11:17186572..17188105-chr11:17229637..17231932,2	K562	blood:
28	chr11:17167469..17170392-chr11:17173847..17176690,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RPS13-3	chr11:17159523-17159812	NONHSAT018216

No data

Variant related genes	Relation type
PIK3C2A	TF binding region
ENSG00000240808	TF binding region
PIK3C2A	CpG island
ENSG00000240808	CpG island
ENSG00000011405	chromatin interactions
ENSG00000267280	chromatin interactions
ENSG00000070081	chromatin interactions
ENSG00000110700	chromatin interactions

Extended variants
information (count: 1624 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:1624 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs34202189	chr11:17151609-17151610	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs565541107	chr11:17151664-17151665	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs140656552	chr11:17151698-17151699	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs183133432	chr11:17151711-17151712	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs537985363	chr11:17151716-17151717	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs554494444	chr11:17151737-17151738	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs183473155	chr11:17151759-17151760	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs78770151	chr11:17151764-17151765	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs559281604	chr11:17151778-17151779	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs577615933	chr11:17151914-17151915	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs537052304	chr11:17151917-17151918	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs545348105	chr11:17151949-17151950	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs564022195	chr11:17152120-17152121	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs1236311	chr11:17152121-17152122	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs549554266	chr11:17152127-17152128	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs189350367	chr11:17152155-17152156	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs193216641	chr11:17152158-17152159	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs185248527	chr11:17152279-17152280	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs190340954	chr11:17152294-17152295	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs571235683	chr11:17152329-17152330	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs538643682	chr11:17152344-17152345	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs550340818	chr11:17152378-17152379	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs181674212	chr11:17152434-17152435	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs569113265	chr11:17152447-17152448	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs536198913	chr11:17152459-17152460	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs554738544	chr11:17152462-17152463	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs554403245	chr11:17152471-17152472	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs371662311	chr11:17152483-17152484	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs572709549	chr11:17152499-17152500	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs185854222	chr11:17152553-17152554	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs553070074	chr11:17152614-17152615	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs188663451	chr11:17152618-17152619	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs545369202	chr11:17152660-17152661	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs11024163	chr11:17152696-17152697	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs180891567	chr11:17152731-17152732	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs540197255	chr11:17152761-17152762	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs78458806	chr11:17152789-17152790	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs75230427	chr11:17152846-17152847	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs561423406	chr11:17152849-17152850	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs116967062	chr11:17152887-17152888	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs141358065	chr11:17152894-17152895	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs112495970	chr11:17152934-17152935	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs149539875	chr11:17152965-17152966	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs68020564	chr11:17152967-17152968	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs398015428	chr11:17152986-17152987	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs111882936	chr11:17153011-17153012	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs151066417	chr11:17153062-17153063	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs377540794	chr11:17153094-17153095	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs576997074	chr11:17153113-17153114	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs544363166	chr11:17153119-17153120	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
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
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Multiple myeloma	16461302	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Lung adenocarcinoma	17086460	CNVD
Urothelial cell carcinoma	18451213	CNVD
Lung cancer	17086460	CNVD
Uterine serous papillary cancer	19536090	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1481 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:17100400-17157200	Weak transcription	Fetal Heart	heart
2	chr11:17105400-17172800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr11:17106800-17156600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr11:17107000-17167200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr11:17108200-17177400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr11:17108600-17172800	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr11:17109800-17158400	Strong transcription	HUES64 Cell Line	embryonic stem cell
8	chr11:17111600-17182000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr11:17111800-17157800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr11:17115800-17154400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
11	chr11:17117800-17151800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
12	chr11:17120400-17157800	Weak transcription	Stomach Mucosa	stomach
13	chr11:17120400-17181600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
14	chr11:17120600-17155800	Weak transcription	Esophagus	oesophagus
15	chr11:17120800-17156200	Weak transcription	Rectal Smooth Muscle	rectum
16	chr11:17120800-17166200	Weak transcription	Pancreas	Pancrea
17	chr11:17120800-17171800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr11:17120800-17172200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr11:17121000-17178000	Weak transcription	Psoas Muscle	Psoas
20	chr11:17125400-17172200	Weak transcription	Fetal Brain Male	brain
21	chr11:17125800-17181400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
22	chr11:17126800-17186400	Weak transcription	Colonic Mucosa	Colon
23	chr11:17129800-17158200	Strong transcription	Primary monocytes fromperipheralblood	blood
24	chr11:17130200-17174600	Weak transcription	Spleen	Spleen
25	chr11:17130200-17203800	Weak transcription	Aorta	Aorta
26	chr11:17132000-17167800	Weak transcription	Right Ventricle	heart
27	chr11:17132200-17155600	Weak transcription	Primary neutrophils fromperipheralblood	blood
28	chr11:17132200-17156200	Weak transcription	HSMMtube	muscle
29	chr11:17132200-17163200	Weak transcription	Brain Cingulate Gyrus	brain
30	chr11:17132800-17154600	Weak transcription	Fetal Thymus	thymus
31	chr11:17135000-17154200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr11:17135000-17155400	Weak transcription	GM12878-XiMat	blood
33	chr11:17135000-17155800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr11:17135200-17155200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr11:17138200-17156000	Weak transcription	Lung	lung
36	chr11:17139000-17171200	Weak transcription	Fetal Brain Female	brain
37	chr11:17139200-17153600	Weak transcription	Skeletal Muscle Male	skeletal muscle
38	chr11:17139400-17154200	Weak transcription	Rectal Mucosa Donor 31	rectum
39	chr11:17140000-17152600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr11:17140000-17155400	Weak transcription	Placenta Amnion	Placenta Amnion
41	chr11:17140000-17183400	Weak transcription	Small Intestine	intestine
42	chr11:17140200-17154200	Weak transcription	Colon Smooth Muscle	Colon
43	chr11:17142800-17156600	Strong transcription	Liver	Liver
44	chr11:17143000-17163800	Weak transcription	Gastric	stomach
45	chr11:17143200-17153000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr11:17143400-17153200	Weak transcription	Cortex derived primary cultured neurospheres	brain
47	chr11:17144200-17192800	Weak transcription	NHDF-Ad	bronchial
48	chr11:17144400-17154800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr11:17144600-17153600	Weak transcription	Stomach Smooth Muscle	stomach
50	chr11:17144600-17166600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood

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