Variant report

Variant	nsv521191
Chromosome Location	chr9:15218947-15246652
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:375)
CpG islands
(count:244)
Chromatin interactive
region (count:8)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:375 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:15232084-15232341	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:15232148-15232279	K562	blood:	n/a	n/a
3	ATF1	chr9:15220876-15221098	K562	blood:	n/a	n/a
4	ATF1	chr9:15232104-15232252	K562	blood:	n/a	n/a
5	BATF	chr9:15228348-15228763	GM12878	blood:	n/a	n/a
6	BATF	chr9:15228358-15228733	GM12878	blood:	n/a	n/a
7	BHLHE40	chr9:15232167-15232259	K562	blood:	n/a	n/a
8	CEBPB	chr9:15239832-15239996	K562	blood:	n/a	chr9:15239852-15239863 chr9:15239934-15239947
9	CEBPB	chr9:15239790-15240099	A549	lung:	n/a	chr9:15239852-15239863 chr9:15239934-15239947
10	CEBPB	chr9:15232414-15232614	HepG2	liver:	n/a	n/a
11	CEBPB	chr9:15243131-15243445	IMR90	lung:	n/a	n/a
12	CEBPB	chr9:15222526-15222776	HepG2	liver:	n/a	chr9:15222628-15222639
13	CEBPB	chr9:15221053-15221446	IMR90	lung:	n/a	n/a
14	CEBPB	chr9:15239837-15240061	Hela-S3	cervix:	n/a	chr9:15239852-15239863 chr9:15239934-15239947
15	CEBPB	chr9:15243971-15244366	IMR90	lung:	n/a	n/a
16	CEBPB	chr9:15221750-15222045	HepG2	liver:	n/a	chr9:15221899-15221912 chr9:15221899-15221910 chr9:15221901-15221912
17	CEBPB	chr9:15239698-15240120	HepG2	liver:	n/a	chr9:15239852-15239863 chr9:15239934-15239947
18	CEBPB	chr9:15232111-15232384	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr9:15239756-15240129	IMR90	lung:	n/a	chr9:15239852-15239863 chr9:15239934-15239947
20	CTCF	chr9:15231740-15231890	HCM	heart:	n/a	n/a
21	CTCF	chr9:15232140-15232290	HL-60	blood:	n/a	n/a
22	CTCF	chr9:15231946-15232372	MCF-7	breast:	n/a	n/a
23	CTCF	chr9:15232087-15232350	MCF-7	breast:	n/a	n/a
24	CTCF	chr9:15239468-15239560	LNCaP	prostate:	n/a	n/a
25	CTCF	chr9:15232140-15232290	AG09309	skin:	n/a	n/a
26	CTCF	chr9:15232090-15232346	LNCaP	prostate:	n/a	n/a
27	CTCF	chr9:15232098-15232335	LNCaP	prostate:	n/a	n/a
28	CTCF	chr9:15232100-15232250	GM12868	blood:	n/a	n/a
29	CTCF	chr9:15232140-15232290	HA-sp	spinal cord:	n/a	n/a
30	CTCF	chr9:15232180-15232330	NHEK	skin:	n/a	n/a
31	CTCF	chr9:15232140-15232290	NB4	blood:	n/a	n/a
32	CTCF	chr9:15225700-15225850	HEEpiC	esophagus:	n/a	n/a
33	CTCF	chr9:15232120-15232270	AG10803	skin:	n/a	n/a
34	CTCF	chr9:15232081-15232358	Fibrobl	skin:	n/a	n/a
35	CTCF	chr9:15232110-15232348	K562	blood:	n/a	n/a
36	CTCF	chr9:15232140-15232290	A549	lung:	n/a	n/a
37	CTCF	chr9:15232120-15232270	AG09319	gingival:	n/a	n/a
38	CTCF	chr9:15232034-15232415	K562	blood:	n/a	n/a
39	CTCF	chr9:15232140-15232290	NHLF	lung:	n/a	n/a
40	CTCF	chr9:15232120-15232270	WERI-Rb-1	eye:	n/a	n/a
41	CTCF	chr9:15231946-15231995	GM19239	blood:	n/a	n/a
42	CTCF	chr9:15232140-15232290	AG09319	gingival:	n/a	n/a
43	CTCF	chr9:15232140-15232290	GM12865	blood:	n/a	n/a
44	CTCF	chr9:15232105-15232379	K562	blood:	n/a	n/a
45	CTCF	chr9:15232744-15232801	GM10266	blood:	n/a	n/a
46	CTCF	chr9:15232100-15232250	HepG2	liver:	n/a	n/a
47	CTCF	chr9:15232160-15232310	HBMEC	blood vessel:	n/a	n/a
48	CTCF	chr9:15232114-15232319	HepG2	liver:	n/a	n/a
49	CTCF	chr9:15231973-15232384	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr9:15231953-15232341	GM12891	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:15232014-15232064	SK-N-SH	brain:	n/a
2	chr9:15232701-15232751	MCF-7	breast:	n/a
3	chr9:15232701-15232751	MCF10A-Er-Src	breast:	n/a
4	chr9:15232701-15232751	H1-hESC	embryonic stem cell:	embryo
5	chr9:15232701-15232751	HAEpiC	amniotic membrane:	n/a
6	chr9:15232701-15232751	HEEpiC	esophagus:	n/a
7	chr9:15232701-15232751	SK-N-SH_RA	brain:	n/a
8	chr9:15232014-15232064	HCT-116	colon:	n/a
9	chr9:15232867-15232917	ProgFib	skin:	n/a
10	chr9:15232867-15232917	BE2_C	brain:	n/a
11	chr9:15236855-15236905	Hela-S3	cervix:	n/a
12	chr9:15232701-15232751	ovcar-3	ovarian:	n/a
13	chr9:15232867-15232917	GM06990	blood:	n/a
14	chr9:15232867-15232917	SK-N-MC	brain:	n/a
15	chr9:15236855-15236905	Caco-2	colon:	n/a
16	chr9:15232701-15232751	GM19239	blood:	n/a
17	chr9:15232014-15232064	BE2_C	brain:	n/a
18	chr9:15232014-15232064	HRCEpiC	kidney:	n/a
19	chr9:15232867-15232917	HRCEpiC	kidney:	n/a
20	chr9:15232867-15232917	Hepatocyte	liver:	n/a
21	chr9:15232014-15232064	HUVEC	blood vessel:	n/a
22	chr9:15236855-15236905	CMK	blood:	n/a
23	chr9:15236855-15236905	SKMC	muscle:	n/a
24	chr9:15236855-15236905	HCM	heart:	n/a
25	chr9:15232014-15232064	HAEpiC	amniotic membrane:	n/a
26	chr9:15232701-15232751	Hela-S3	cervix:	n/a
27	chr9:15232867-15232917	H1-hESC	embryonic stem cell:	embryo
28	chr9:15232014-15232064	K562	blood:	n/a
29	chr9:15232014-15232064	U87	brain:	n/a
30	chr9:15236855-15236905	Hepatocyte	liver:	n/a
31	chr9:15232701-15232751	NHBE	bronchial:	n/a
32	chr9:15236855-15236905	AG09309	skin:	n/a
33	chr9:15232014-15232064	AG10803	skin:	n/a
34	chr9:15236855-15236905	HCF	heart:	n/a
35	chr9:15236855-15236905	T-47D	breast:	n/a
36	chr9:15232014-15232064	PrEC	prostate:	n/a
37	chr9:15232701-15232751	CMK	blood:	n/a
38	chr9:15232867-15232917	K562	blood:	n/a
39	chr9:15232867-15232917	BJ	skin:	n/a
40	chr9:15236855-15236905	HEEpiC	esophagus:	n/a
41	chr9:15232014-15232064	SKMC	muscle:	n/a
42	chr9:15232014-15232064	ECC-1	luminal epithelium:	n/a
43	chr9:15232701-15232751	HIPEpiC	eye:	n/a
44	chr9:15232867-15232917	AG09319	gingival:	n/a
45	chr9:15236855-15236905	PrEC	prostate:	n/a
46	chr9:15232014-15232064	ProgFib	skin:	n/a
47	chr9:15232701-15232751	HCF	heart:	n/a
48	chr9:15232701-15232751	AG09319	gingival:	n/a
49	chr9:15232014-15232064	MCF10A-Er-Src	breast:	n/a
50	chr9:15232867-15232917	HRPEpiC	eye:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:15218010..15219971-chr9:15288500..15290967,2	MCF-7	breast:
2	chr9:15232176..15234020-chr9:15242735..15245589,2	MCF-7	breast:
3	chr9:15238862..15241119-chr9:15243843..15246423,2	MCF-7	breast:
4	chr9:15240990..15244433-chr9:15303373..15307437,3	MCF-7	breast:
5	chr9:15235538..15237507-chr9:117160951..117163548,2	MCF-7	breast:
6	chr9:15180910..15183220-chr9:15227592..15229851,2	MCF-7	breast:
7	chr9:15242669..15244431-chr9:15422825..15424488,2	MCF-7	breast:
8	chr9:15238862..15241119-chr9:15243843..15246423,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PSIP1-3	chr9:15225915-15226010	NONHSAT130261
2	lnc-PSIP1-3	chr9:15224358-15224503	NONHSAT130261
3	lnc-PSIP1-3	chr9:15232230-15232442	NONHSAT130261

No data

Variant related genes	Relation type
TTC39B	TF binding region
TTC39B	CpG island
ENSG00000164975	chromatin interactions
ENSG00000155158	chromatin interactions

Extended variants
information (count: 1257 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:1257 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7870690	chr9:15218947-15218948	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs189444392	chr9:15218949-15218950	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs373086107	chr9:15218987-15218988	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs561357464	chr9:15218991-15218992	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs574825	chr9:15219015-15219016	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs528813564	chr9:15219063-15219064	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs544165676	chr9:15219114-15219115	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs550284726	chr9:15219158-15219159	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs116649666	chr9:15219164-15219165	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs542768407	chr9:15219219-15219220	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs192958196	chr9:15219265-15219266	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs551331031	chr9:15219287-15219288	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs566647763	chr9:15219290-15219291	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs559545436	chr9:15219293-15219294	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs533852294	chr9:15219300-15219301	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs185217054	chr9:15219324-15219325	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs147261307	chr9:15219352-15219353	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs538207570	chr9:15219354-15219355	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs577643	chr9:15219359-15219360	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs140511631	chr9:15219365-15219366	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs545481161	chr9:15219376-15219377	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs554112119	chr9:15219395-15219396	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs116366291	chr9:15219410-15219411	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs189643346	chr9:15219425-15219426	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs561219687	chr9:15219434-15219435	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs528878128	chr9:15219446-15219447	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs79615359	chr9:15219483-15219484	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs562125173	chr9:15219494-15219495	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs142791228	chr9:15219538-15219539	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs551411539	chr9:15219587-15219588	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs144629253	chr9:15219589-15219590	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs527448275	chr9:15219617-15219618	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs115682355	chr9:15219619-15219620	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs528532518	chr9:15219621-15219622	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs75353774	chr9:15219622-15219623	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs538122830	chr9:15219627-15219628	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs556636137	chr9:15219632-15219633	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs148491314	chr9:15219644-15219645	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs538758228	chr9:15219842-15219843	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs554196850	chr9:15219843-15219844	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs142672136	chr9:15219845-15219846	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs181175021	chr9:15219869-15219870	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs554719388	chr9:15219881-15219882	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs4741478	chr9:15219882-15219883	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs150944307	chr9:15219884-15219885	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs373803522	chr9:15219896-15219897	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs139806336	chr9:15219899-15219900	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs577527185	chr9:15219911-15219912	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs185092144	chr9:15219941-15219942	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs201462449	chr9:15219946-15219947	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Melanoma	18172304	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Myelodysplastic syndrome	21251322	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	18803288	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21611746	CNVD
Glycine encephalopathy	21572526	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	19835627	CNVD
early-passage human iPS cells	21368824	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD

Chromatin state (count:474 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:15163000-15233000	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr9:15171000-15228600	Weak transcription	Stomach Mucosa	stomach
3	chr9:15179400-15221000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr9:15182200-15229200	Weak transcription	Gastric	stomach
5	chr9:15185600-15225800	Weak transcription	Pancreas	Pancrea
6	chr9:15192200-15229200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
7	chr9:15192400-15223200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
8	chr9:15193400-15249600	Weak transcription	Colonic Mucosa	Colon
9	chr9:15197200-15223000	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr9:15197200-15225000	Weak transcription	Monocytes-CD14+_RO01746	blood
11	chr9:15206000-15220800	Weak transcription	Lung	lung
12	chr9:15206000-15222800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
13	chr9:15206000-15223000	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr9:15206000-15229200	Weak transcription	Ovary	ovary
15	chr9:15206400-15221000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr9:15207600-15225600	Weak transcription	Primary B cells from peripheral blood	blood
17	chr9:15207800-15223000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr9:15209600-15223000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
19	chr9:15210000-15231800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
20	chr9:15210600-15226200	Weak transcription	Primary hematopoietic stem cells	blood
21	chr9:15211000-15222400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr9:15211200-15222000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
23	chr9:15211400-15222600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
24	chr9:15211400-15222600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
25	chr9:15211400-15229000	Weak transcription	Primary T helper cells PMA-I stimulated	--
26	chr9:15211400-15229000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
27	chr9:15211600-15223200	Weak transcription	Stomach Smooth Muscle	stomach
28	chr9:15211600-15224600	Weak transcription	NHEK	skin
29	chr9:15211600-15226600	Weak transcription	HMEC	breast
30	chr9:15211800-15220800	Weak transcription	Adipose Nuclei	Adipose
31	chr9:15212000-15219400	Weak transcription	Fetal Kidney	kidney
32	chr9:15212000-15220200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr9:15212000-15222400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr9:15212000-15222400	Weak transcription	Fetal Stomach	stomach
35	chr9:15212000-15222800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
36	chr9:15212000-15224800	Weak transcription	Rectal Smooth Muscle	rectum
37	chr9:15212000-15225400	Weak transcription	Brain Inferior Temporal Lobe	brain
38	chr9:15212200-15220200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr9:15212200-15220800	Weak transcription	Muscle Satellite Cultured Cells	--
40	chr9:15212400-15220800	Weak transcription	Aorta	Aorta
41	chr9:15212400-15223000	Weak transcription	Fetal Lung	lung
42	chr9:15212400-15225600	Weak transcription	Duodenum Smooth Muscle	Duodenum
43	chr9:15212800-15226000	Weak transcription	Liver	Liver
44	chr9:15213400-15222600	Weak transcription	HepG2	liver
45	chr9:15213600-15225800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
46	chr9:15214200-15219200	Weak transcription	Duodenum Mucosa	Duodenum
47	chr9:15214800-15222200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr9:15214800-15222600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
49	chr9:15214800-15226000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
50	chr9:15215200-15219200	Weak transcription	Fetal Intestine Small	intestine

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