Variant report

Variant	nsv430095
Chromosome Location	chr9:117073446-117095446
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:500)
CpG islands
(count:305)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:500 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:117091599-117091832	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:117084358-117084903	HepG2	liver:	n/a	n/a
3	ATF1	chr9:117080165-117080332	K562	blood:	n/a	n/a
4	ATF3	chr9:117080162-117080453	K562	blood:	n/a	n/a
5	BCL3	chr9:117094659-117095275	GM12878	blood:	n/a	n/a
6	BCL3	chr9:117080178-117080438	GM12878	blood:	n/a	n/a
7	BCL3	chr9:117080117-117080458	GM12878	blood:	n/a	n/a
8	BCL3	chr9:117094739-117094968	GM12878	blood:	n/a	n/a
9	BHLHE40	chr9:117085114-117085542	HepG2	liver:	n/a	n/a
10	BHLHE40	chr9:117091885-117092313	HepG2	liver:	n/a	n/a
11	BHLHE40	chr9:117084718-117085030	HepG2	liver:	n/a	n/a
12	CBX3	chr9:117089360-117089769	K562	blood:	n/a	n/a
13	CEBPB	chr9:117091524-117091772	HepG2	liver:	n/a	n/a
14	CEBPB	chr9:117080119-117080474	A549	lung:	n/a	chr9:117080273-117080284
15	CEBPB	chr9:117084795-117084978	HepG2	liver:	n/a	n/a
16	CEBPB	chr9:117080214-117080319	HepG2	liver:	n/a	chr9:117080273-117080284
17	CEBPB	chr9:117080097-117080535	Hela-S3	cervix:	n/a	chr9:117080273-117080284
18	CEBPB	chr9:117080205-117080383	K562	blood:	n/a	chr9:117080273-117080284
19	CEBPB	chr9:117077520-117077679	IMR90	lung:	n/a	chr9:117077571-117077582 chr9:117077573-117077582 chr9:117077571-117077584
20	CEBPB	chr9:117091468-117091849	HepG2	liver:	n/a	n/a
21	CEBPB	chr9:117091269-117091840	HepG2	liver:	n/a	n/a
22	CEBPB	chr9:117084690-117085081	HepG2	liver:	n/a	n/a
23	CEBPB	chr9:117084691-117085065	HepG2	liver:	n/a	n/a
24	CEBPB	chr9:117080082-117080511	IMR90	lung:	n/a	chr9:117080273-117080284
25	CEBPB	chr9:117080094-117080487	K562	blood:	n/a	chr9:117080273-117080284
26	CEBPB	chr9:117078053-117078318	HepG2	liver:	n/a	n/a
27	CEBPB	chr9:117084769-117085000	HepG2	liver:	n/a	n/a
28	CEBPB	chr9:117080115-117080579	A549	lung:	n/a	chr9:117080273-117080284
29	CEBPB	chr9:117091567-117091727	HepG2	liver:	n/a	n/a
30	CEBPB	chr9:117077405-117077763	HepG2	liver:	n/a	chr9:117077571-117077582 chr9:117077573-117077582 chr9:117077571-117077584
31	CEBPB	chr9:117080094-117080477	HepG2	liver:	n/a	chr9:117080273-117080284
32	CEBPB	chr9:117080076-117080472	K562	blood:	n/a	chr9:117080273-117080284
33	CEBPD	chr9:117080879-117081604	K562	blood:	n/a	n/a
34	CEBPD	chr9:117091543-117091776	HepG2	liver:	n/a	n/a
35	CHD2	chr9:117085014-117085045	HepG2	liver:	n/a	n/a
36	CTCF	chr9:117085375-117085432	HepG2	liver:	n/a	chr9:117085397-117085407
37	CTCF	chr9:117074232-117074236	Lung_OC	lung:	n/a	n/a
38	CTCF	chr9:117080200-117080350	AG10803	skin:	n/a	n/a
39	CTCF	chr9:117087295-117087347	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr9:117094063-117094136	K562	blood:	n/a	n/a
41	CTCF	chr9:117080330-117080340	IMR90	lung:	n/a	n/a
42	CTCF	chr9:117085337-117085354	Lung_OC	lung:	n/a	n/a
43	CTCF	chr9:117079160-117079310	WERI-Rb-1	eye:	n/a	n/a
44	CTCF	chr9:117074237-117074291	Lung_OC	lung:	n/a	n/a
45	CTCF	chr9:117079180-117079330	WERI-Rb-1	eye:	n/a	n/a
46	CTCF	chr9:117090740-117090890	HEEpiC	esophagus:	n/a	n/a
47	CUX1	chr9:117086263-117086283	K562	blood:	n/a	n/a
48	E2F4	chr9:117080332-117080426	MCF10A-Er-Src	breast:	n/a	n/a
49	EGR1	chr9:117080497-117080836	K562	blood:	n/a	n/a
50	EP300	chr9:117084601-117085068	HepG2	liver:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:117084602-117084652	Hela-S3	cervix:	n/a
2	chr9:117084602-117084652	HRE	kidney:	n/a
3	chr9:117084602-117084652	HNPCEpiC	eye:	n/a
4	chr9:117093052-117093102	RPTEC	kidney:	n/a
5	chr9:117093175-117093225	GM19239	blood:	n/a
6	chr9:117093052-117093102	AG04450	lung:	fetal
7	chr9:117093052-117093102	GM19239	blood:	n/a
8	chr9:117093052-117093102	PFSK-1	brain:	n/a
9	chr9:117093175-117093225	HCM	heart:	n/a
10	chr9:117085966-117086016	GM12891	blood:	n/a
11	chr9:117093175-117093225	HNPCEpiC	eye:	n/a
12	chr9:117090924-117090974	GM12891	blood:	n/a
13	chr9:117085966-117086016	HL-60	blood:	n/a
14	chr9:117084602-117084652	RPTEC	kidney:	n/a
15	chr9:117085966-117086016	HepG2	liver:	n/a
16	chr9:117093175-117093225	Hepatocyte	liver:	n/a
17	chr9:117093052-117093102	SK-N-SH_RA	brain:	n/a
18	chr9:117093052-117093102	HRCEpiC	kidney:	n/a
19	chr9:117093052-117093102	CMK	blood:	n/a
20	chr9:117085966-117086016	HEEpiC	esophagus:	n/a
21	chr9:117090924-117090974	AoSMC	blood vessel:	n/a
22	chr9:117093175-117093225	NHBE	bronchial:	n/a
23	chr9:117090924-117090974	NB4	blood:	n/a
24	chr9:117090924-117090974	NH-A	brain:	n/a
25	chr9:117090924-117090974	U87	brain:	n/a
26	chr9:117093175-117093225	AG09319	gingival:	n/a
27	chr9:117090924-117090974	GM19239	blood:	n/a
28	chr9:117090924-117090974	HepG2	liver:	n/a
29	chr9:117090924-117090974	HPAEpiC	pulmonary alveolar:	n/a
30	chr9:117093175-117093225	LNCaP	prostate:	n/a
31	chr9:117090924-117090974	H1-hESC	embryonic stem cell:	embryo
32	chr9:117084602-117084652	ProgFib	skin:	n/a
33	chr9:117085966-117086016	H1-hESC	embryonic stem cell:	embryo
34	chr9:117084602-117084652	MCF-7	breast:	n/a
35	chr9:117090924-117090974	SAEC	small airway:	n/a
36	chr9:117093052-117093102	HCPEpiC	choroid plexus:	n/a
37	chr9:117085966-117086016	Caco-2	colon:	n/a
38	chr9:117093175-117093225	HPAEpiC	pulmonary alveolar:	n/a
39	chr9:117085966-117086016	SK-N-SH	brain:	n/a
40	chr9:117093175-117093225	Jurkat	blood:	n/a
41	chr9:117084602-117084652	H1-hESC	embryonic stem cell:	embryo
42	chr9:117084602-117084652	HMEC	breast:	n/a
43	chr9:117085966-117086016	AG10803	skin:	n/a
44	chr9:117093175-117093225	PANC-1	pancreas:	n/a
45	chr9:117085966-117086016	AG09319	gingival:	n/a
46	chr9:117085966-117086016	NH-A	brain:	n/a
47	chr9:117090924-117090974	HIPEpiC	eye:	n/a
48	chr9:117093175-117093225	IMR90	lung:	fetal
49	chr9:117085966-117086016	T-47D	breast:	n/a
50	chr9:117084602-117084652	GM12878	blood:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:117066557..117068874-chr9:117077753..117079545,2	MCF-7	breast:
2	chr9:117086796..117090916-chr9:117093612..117097049,4	K562	blood:
3	chr9:117073544..117075822-chr9:117160051..117162438,2	K562	blood:
4	chr9:117086796..117090916-chr9:117093612..117097049,4	K562	blood:

No data

Variant related genes	Relation type
ORM1	TF binding region
ORM2	TF binding region
ORM1	CpG island
ORM2	CpG island
ENSG00000196739	chromatin interactions
ENSG00000235119	chromatin interactions

Extended variants
information (count: 1193 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:1193 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs188133091	chr9:117073456-117073457	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs576097310	chr9:117073457-117073458	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs190134664	chr9:117073472-117073473	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs556029568	chr9:117073480-117073481	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs534309297	chr9:117073494-117073495	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs7033547	chr9:117073508-117073509	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs374074003	chr9:117073535-117073536	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs564496373	chr9:117073545-117073546	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs533496892	chr9:117073552-117073553	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs543497572	chr9:117073561-117073562	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs555273838	chr9:117073582-117073583	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs11537824	chr9:117073588-117073589	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs141414252	chr9:117073620-117073621	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs149632411	chr9:117073622-117073623	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs368919450	chr9:117073624-117073625	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs71718212	chr9:117073629-117073630	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs111227183	chr9:117073634-117073635	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs10699253	chr9:117073635-117073636	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs529250283	chr9:117073692-117073693	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs182043178	chr9:117073704-117073705	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs186720815	chr9:117073705-117073706	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs527561488	chr9:117073737-117073738	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs571168699	chr9:117073774-117073775	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs570537954	chr9:117073775-117073776	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs201499465	chr9:117073815-117073816	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs369258709	chr9:117073820-117073821	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs373920076	chr9:117073827-117073828	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs372528034	chr9:117073828-117073829	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs56094843	chr9:117073829-117073830	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs397976494	chr9:117073845-117073846	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs543761373	chr9:117073932-117073933	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs540082463	chr9:117073933-117073934	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs10982143	chr9:117073954-117073955	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs552789939	chr9:117073956-117073957	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs539581715	chr9:117073963-117073964	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs558029856	chr9:117074001-117074002	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs59477952	chr9:117074036-117074037	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs16928063	chr9:117074052-117074053	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs113907809	chr9:117074113-117074114	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs577659010	chr9:117074118-117074119	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs535452485	chr9:117074139-117074140	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs368139320	chr9:117074140-117074141	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs192359059	chr9:117074145-117074146	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs78512345	chr9:117074154-117074155	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs141631486	chr9:117074162-117074163	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs558366647	chr9:117074175-117074176	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs577809557	chr9:117074186-117074187	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs115415349	chr9:117074191-117074192	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs563448834	chr9:117074212-117074213	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs7465888	chr9:117074214-117074215	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
small cell lung cancer	20016488	CNVD
Cardiac fibroma	18329553	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
Lung cancer	19147751	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16272173	CNVD
Bladder cancer	21909424	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	21509527	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Cervical cancer	16585170	CNVD
Ependymoma	19289631	CNVD
Melanoma	17363583	CNVD
Retinoblastoma	19183342	CNVD

Chromatin state (count:416 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:117028200-117077000	Weak transcription	Gastric	stomach
2	chr9:117039800-117076600	Weak transcription	Lung	lung
3	chr9:117043800-117074800	Strong transcription	Fetal Intestine Large	intestine
4	chr9:117043800-117075200	Weak transcription	Rectal Smooth Muscle	rectum
5	chr9:117051200-117097200	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr9:117051400-117086800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr9:117053200-117075000	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr9:117053200-117075400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr9:117054800-117077800	Weak transcription	Stomach Mucosa	stomach
10	chr9:117057400-117073600	Weak transcription	Colon Smooth Muscle	Colon
11	chr9:117057400-117075400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr9:117058000-117077800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr9:117058400-117075000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr9:117058600-117080200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr9:117058800-117074400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
16	chr9:117059000-117089800	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr9:117060400-117080600	Weak transcription	HSMM	muscle
18	chr9:117061000-117110000	Weak transcription	A549	lung
19	chr9:117061200-117073600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr9:117061200-117074800	Strong transcription	Fetal Intestine Small	intestine
21	chr9:117061200-117075400	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr9:117061200-117081200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr9:117061800-117077400	Weak transcription	Adipose Nuclei	Adipose
24	chr9:117062800-117075200	Weak transcription	HMEC	breast
25	chr9:117062800-117076400	Weak transcription	Fetal Kidney	kidney
26	chr9:117062800-117084400	Weak transcription	NH-A	brain
27	chr9:117063400-117076000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
28	chr9:117063400-117077400	Weak transcription	HUVEC	blood vessel
29	chr9:117064800-117076800	Weak transcription	Duodenum Smooth Muscle	Duodenum
30	chr9:117065400-117074800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr9:117068000-117078800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr9:117068200-117074200	Strong transcription	HepG2	liver
33	chr9:117068200-117074600	Weak transcription	Brain Substantia Nigra	brain
34	chr9:117068200-117075000	Strong transcription	Fetal Stomach	stomach
35	chr9:117068200-117075000	Weak transcription	Left Ventricle	heart
36	chr9:117068200-117075800	Weak transcription	Duodenum Mucosa	Duodenum
37	chr9:117068200-117076600	Weak transcription	Skeletal Muscle Male	skeletal muscle
38	chr9:117068200-117076800	Weak transcription	Skeletal Muscle Female	skeletal muscle
39	chr9:117068400-117074800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr9:117068400-117076600	Weak transcription	Right Ventricle	heart
41	chr9:117068600-117075000	Strong transcription	Fetal Muscle Leg	muscle
42	chr9:117068800-117075200	Strong transcription	Fetal Muscle Trunk	muscle
43	chr9:117068800-117084400	Weak transcription	Ovary	ovary
44	chr9:117070200-117075000	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr9:117070200-117075200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr9:117070200-117075800	Weak transcription	NHLF	lung
47	chr9:117070600-117083200	Weak transcription	Osteobl	bone
48	chr9:117070800-117079200	Weak transcription	HUES6 Cell Line	embryonic stem cell
49	chr9:117070800-117080400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr9:117071000-117073800	Strong transcription	Liver	Liver

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