Variant report

Variant	nsv831700
Chromosome Location	chr9:118683827-118834499
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1543)
CpG islands
(count:183)
Chromatin interactive
region (count:11)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1543 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:118758807-118759123	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:118708827-118709267	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:118763138-118763398	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:118706133-118707355	HepG2	liver:	n/a	n/a
5	ARID3A	chr9:118715033-118715240	HepG2	liver:	n/a	n/a
6	ATF3	chr9:118758663-118759138	A549	lung:	n/a	n/a
7	ATF3	chr9:118706381-118707440	A549	lung:	n/a	chr9:118707028-118707042
8	ATF3	chr9:118708775-118709352	A549	lung:	n/a	chr9:118709072-118709080
9	ATF3	chr9:118686166-118686684	A549	lung:	n/a	n/a
10	ATF3	chr9:118734895-118735570	A549	lung:	n/a	n/a
11	ATF3	chr9:118685936-118686685	A549	lung:	n/a	n/a
12	ATF3	chr9:118706268-118707532	A549	lung:	n/a	chr9:118707028-118707042
13	ATF3	chr9:118735028-118735509	A549	lung:	n/a	n/a
14	BACH1	chr9:118789896-118789959	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr9:118764933-118765166	K562	blood:	n/a	n/a
16	BACH1	chr9:118764879-118765157	H1-hESC	embryonic stem cell:	n/a	n/a
17	BCL3	chr9:118758669-118759200	A549	lung:	n/a	n/a
18	BCL3	chr9:118758590-118759229	A549	lung:	n/a	n/a
19	BCL3	chr9:118735004-118735586	A549	lung:	n/a	n/a
20	BCL3	chr9:118714798-118715523	A549	lung:	n/a	n/a
21	BCL3	chr9:118701157-118701699	A549	lung:	n/a	n/a
22	BCL3	chr9:118685994-118686701	A549	lung:	n/a	n/a
23	BCL3	chr9:118708631-118709394	A549	lung:	n/a	chr9:118709256-118709265
24	BCL3	chr9:118706265-118707754	A549	lung:	n/a	n/a
25	BCL3	chr9:118708781-118709315	A549	lung:	n/a	chr9:118709256-118709265
26	BCL3	chr9:118685961-118686927	A549	lung:	n/a	n/a
27	BCL3	chr9:118706204-118707925	A549	lung:	n/a	n/a
28	BCL3	chr9:118734637-118735683	A549	lung:	n/a	n/a
29	BCL3	chr9:118714789-118715430	A549	lung:	n/a	n/a
30	BHLHE40	chr9:118708839-118709230	HepG2	liver:	n/a	n/a
31	BHLHE40	chr9:118708866-118709191	A549	lung:	n/a	n/a
32	BHLHE40	chr9:118760382-118760595	GM12878	blood:	n/a	n/a
33	BHLHE40	chr9:118706495-118707516	HepG2	liver:	n/a	n/a
34	BHLHE40	chr9:118701345-118701648	A549	lung:	n/a	n/a
35	BHLHE40	chr9:118706627-118707268	A549	lung:	n/a	n/a
36	BRCA1	chr9:118701365-118702010	Hela-S3	cervix:	n/a	n/a
37	BRCA1	chr9:118706442-118707371	Hela-S3	cervix:	n/a	n/a
38	BRCA1	chr9:118686225-118686584	Hela-S3	cervix:	n/a	n/a
39	CBX3	chr9:118762862-118763438	HCT-116	colon:	n/a	n/a
40	CBX3	chr9:118770016-118771122	HCT-116	colon:	n/a	n/a
41	CCNT2	chr9:118713189-118713365	K562	blood:	n/a	n/a
42	CCNT2	chr9:118758920-118759120	K562	blood:	n/a	n/a
43	CCNT2	chr9:118690119-118690319	K562	blood:	n/a	n/a
44	CCNT2	chr9:118784298-118784653	K562	blood:	n/a	n/a
45	CEBPB	chr9:118708842-118709276	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr9:118697437-118697564	IMR90	lung:	n/a	n/a
47	CEBPB	chr9:118701208-118701961	A549	lung:	n/a	chr9:118701491-118701500 chr9:118701491-118701500 chr9:118701780-118701791 chr9:118701491-118701500 chr9:118701489-118701502 chr9:118701491-118701500 chr9:118701489-118701502
48	CEBPB	chr9:118683497-118683989	HepG2	liver:	n/a	chr9:118683829-118683838 chr9:118683829-118683838 chr9:118683829-118683838 chr9:118683829-118683838 chr9:118683653-118683662 chr9:118683829-118683840 chr9:118683653-118683662
49	CEBPB	chr9:118706433-118707323	HepG2	liver:	n/a	chr9:118707095-118707112 chr9:118707096-118707109 chr9:118707127-118707138 chr9:118707097-118707108
50	CEBPB	chr9:118748109-118748409	IMR90	lung:	n/a	chr9:118748229-118748240 chr9:118748209-118748221 chr9:118748262-118748273

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:118687694-118687744	HCM	heart:	n/a
2	chr9:118687465-118687515	GM12891	blood:	n/a
3	chr9:118687943-118687993	A549	lung:	n/a
4	chr9:118687694-118687744	HRCEpiC	kidney:	n/a
5	chr9:118687465-118687515	SKMC	muscle:	n/a
6	chr9:118687943-118687993	H1-hESC	embryonic stem cell:	embryo
7	chr9:118687943-118687993	HCPEpiC	choroid plexus:	n/a
8	chr9:118687465-118687515	HRE	kidney:	n/a
9	chr9:118687694-118687744	A549	lung:	n/a
10	chr9:118687943-118687993	IMR90	lung:	fetal
11	chr9:118687943-118687993	NHDF-neo	bronchial:	n/a
12	chr9:118687943-118687993	AG04450	lung:	fetal
13	chr9:118687465-118687515	HEEpiC	esophagus:	n/a
14	chr9:118687943-118687993	BE2_C	brain:	n/a
15	chr9:118687943-118687993	ECC-1	luminal epithelium:	n/a
16	chr9:118687694-118687744	AG09309	skin:	n/a
17	chr9:118687694-118687744	RPTEC	kidney:	n/a
18	chr9:118687943-118687993	HRE	kidney:	n/a
19	chr9:118687694-118687744	U87	brain:	n/a
20	chr9:118687694-118687744	PrEC	prostate:	n/a
21	chr9:118687694-118687744	T-47D	breast:	n/a
22	chr9:118687694-118687744	HEK293	kidney:	embryo
23	chr9:118687465-118687515	GM19239	blood:	n/a
24	chr9:118687694-118687744	PFSK-1	brain:	n/a
25	chr9:118687694-118687744	HAEpiC	amniotic membrane:	n/a
26	chr9:118687943-118687993	NHBE	bronchial:	n/a
27	chr9:118687943-118687993	HCT-116	colon:	n/a
28	chr9:118687465-118687515	BJ	skin:	n/a
29	chr9:118687694-118687744	HMEC	breast:	n/a
30	chr9:118687694-118687744	GM06990	blood:	n/a
31	chr9:118687694-118687744	NH-A	brain:	n/a
32	chr9:118687694-118687744	LNCaP	prostate:	n/a
33	chr9:118687465-118687515	HL-60	blood:	n/a
34	chr9:118687465-118687515	AG04450	lung:	fetal
35	chr9:118687694-118687744	BE2_C	brain:	n/a
36	chr9:118687465-118687515	HepG2	liver:	n/a
37	chr9:118687943-118687993	HEEpiC	esophagus:	n/a
38	chr9:118687465-118687515	HCPEpiC	choroid plexus:	n/a
39	chr9:118687943-118687993	HepG2	liver:	n/a
40	chr9:118687943-118687993	CMK	blood:	n/a
41	chr9:118687465-118687515	ECC-1	luminal epithelium:	n/a
42	chr9:118687465-118687515	U87	brain:	n/a
43	chr9:118687694-118687744	NHDF-neo	bronchial:	n/a
44	chr9:118687465-118687515	ProgFib	skin:	n/a
45	chr9:118687943-118687993	AG09319	gingival:	n/a
46	chr9:118687465-118687515	GM12892	blood:	n/a
47	chr9:118687465-118687515	AG09309	skin:	n/a
48	chr9:118687465-118687515	H1-hESC	embryonic stem cell:	embryo
49	chr9:118687694-118687744	GM19239	blood:	n/a
50	chr9:118687465-118687515	PrEC	prostate:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr12:90103727..90105965-chr9:118735035..118737776,2	MCF-7	breast:
2	chr9:118807555..118809349-chr9:118809413..118812280,2	K562	blood:
3	chr9:118789505..118792191-chr9:118846950..118848695,2	K562	blood:
4	chr9:118765127..118767684-chr9:118769235..118771481,2	K562	blood:
5	chr9:118702732..118704840-chr9:118725161..118727624,2	MCF-7	breast:
6	chr9:118715065..118717508-chr9:118718112..118721109,3	MCF-7	breast:
7	chr9:118807555..118809349-chr9:118809413..118812280,2	K562	blood:
8	chr9:118765127..118767684-chr9:118769235..118771481,2	K562	blood:
9	chr9:118313061..118314706-chr9:118831781..118833432,2	MCF-7	breast:
10	chr9:118702732..118704840-chr9:118725161..118727624,2	MCF-7	breast:
11	chr9:118715065..118717508-chr9:118718112..118721109,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PAPPA-AS1-3	chr9:118687302-118687377	NR_024032
2	lnc-PAPPA-1	chr9:118774640-118774809	XLOC_007534
3	lnc-PAPPA-AS1-3	chr9:118687302-118687486	ENSG00000204148
4	lnc-PAPPA-1	chr9:118774906-118775244	XLOC_007534
5	lnc-PAPPA-AS1-3	chr9:118687302-118687377	XLOC_007836

No data

Variant related genes	Relation type
LINC00474	TF binding region
ENSG00000228707	TF binding region
LINC00474	CpG island
ENSG00000228707	CpG island
PLAGL2	miRNA target sites
APAF1	miRNA target sites
SMAD1	miRNA target sites

Extended variants
information (count: 5265 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:5265 , 50 per page) page: 1 2 3 4 5 6 7 ... 106

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs560523535	chr9:118683852-118683853	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs144942637	chr9:118683854-118683855	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs116593195	chr9:118683856-118683857	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs10983013	chr9:118683862-118683863	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs78797213	chr9:118683875-118683876	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs531753873	chr9:118683884-118683885	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs377764648	chr9:118683894-118683895	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs35052145	chr9:118683912-118683913	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs183861738	chr9:118683959-118683960	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs531013368	chr9:118683977-118683978	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs117194055	chr9:118683980-118683981	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs529168914	chr9:118684023-118684024	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs547662597	chr9:118684042-118684043	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs567655900	chr9:118684147-118684148	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs112541274	chr9:118684176-118684177	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs141745452	chr9:118684181-118684182	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs150046158	chr9:118684182-118684183	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs188244969	chr9:118684183-118684184	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs370847780	chr9:118684187-118684188	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs10817849	chr9:118684189-118684190	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs553738835	chr9:118684251-118684252	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs11999077	chr9:118684268-118684269	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs537051885	chr9:118684277-118684278	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs554181909	chr9:118684281-118684282	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs574100470	chr9:118684282-118684283	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs149164864	chr9:118684296-118684297	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs560033939	chr9:118684309-118684310	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs532410209	chr9:118684346-118684347	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs188095	chr9:118684351-118684352	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs545708732	chr9:118684370-118684371	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs201898218	chr9:118684375-118684376	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs562688721	chr9:118684376-118684377	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs556691377	chr9:118684378-118684379	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs67694964	chr9:118684379-118684380	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs66481541	chr9:118684382-118684383	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs530948780	chr9:118684432-118684433	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs555022366	chr9:118684445-118684446	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs567715206	chr9:118684456-118684457	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs530124897	chr9:118684475-118684476	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs546980919	chr9:118684518-118684519	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs374080443	chr9:118684522-118684523	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs377137802	chr9:118684533-118684534	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs71505563	chr9:118684547-118684548	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs180946902	chr9:118684581-118684582	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs77711881	chr9:118684615-118684616	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs568775342	chr9:118684629-118684630	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs185892547	chr9:118684639-118684640	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs569420745	chr9:118684647-118684648	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs386737946	chr9:118684790-118684791	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs9299235	chr9:118684791-118684792	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:67)

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
Breast cancer	21509527	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Cervical cancer	16585170	CNVD
Ependymoma	19289631	CNVD
Schizophrenia	18940311	CNVD
Neuroticism	17667963	CNVD
Cervical cancer	17311676	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Neurodevelopmental disorder	0	CNVD
Intellectual disability	21811512	CNVD
Schizophrenia	20838587	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:743 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:118679800-118684000	Weak transcription	Placenta	Placenta
2	chr9:118683200-118684000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr9:118683200-118684000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr9:118683200-118684000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr9:118683200-118684000	Enhancers	Muscle Satellite Cultured Cells	--
6	chr9:118683200-118686800	Enhancers	Osteobl	bone
7	chr9:118683400-118684000	Enhancers	NHDF-Ad	bronchial
8	chr9:118683400-118684200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr9:118683400-118684200	Enhancers	NHLF	lung
10	chr9:118683400-118688200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr9:118683800-118688000	Enhancers	Hela-S3	cervix
12	chr9:118683800-118688200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr9:118684000-118685400	Weak transcription	NHDF-Ad	bronchial
14	chr9:118684000-118685600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr9:118684000-118685600	Weak transcription	Muscle Satellite Cultured Cells	--
16	chr9:118684000-118685800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr9:118684000-118686200	Enhancers	Placenta	Placenta
18	chr9:118684200-118685400	Weak transcription	NHLF	lung
19	chr9:118684400-118685600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr9:118684600-118685600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr9:118684800-118685600	Enhancers	A549	lung
22	chr9:118685400-118687000	Enhancers	NHDF-Ad	bronchial
23	chr9:118685400-118687400	Enhancers	NHLF	lung
24	chr9:118685400-118687800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr9:118685600-118686200	Flanking Active TSS	A549	lung
26	chr9:118685600-118686800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr9:118685600-118686800	Enhancers	NH-A	brain
28	chr9:118685600-118687000	Enhancers	Muscle Satellite Cultured Cells	--
29	chr9:118685600-118687000	Enhancers	Liver	Liver
30	chr9:118685800-118686800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr9:118685800-118686800	Enhancers	Duodenum Smooth Muscle	Duodenum
32	chr9:118685800-118687400	Enhancers	Fetal Lung	lung
33	chr9:118686000-118686600	Enhancers	Right Ventricle	heart
34	chr9:118686200-118686600	Active TSS	A549	lung
35	chr9:118686200-118686800	Enhancers	HepG2	liver
36	chr9:118686200-118687600	Active TSS	Placenta	Placenta
37	chr9:118686600-118687400	Flanking Active TSS	A549	lung
38	chr9:118687400-118687800	Enhancers	A549	lung
39	chr9:118687400-118692600	Weak transcription	NHLF	lung
40	chr9:118687600-118687800	Flanking Active TSS	Placenta	Placenta
41	chr9:118687800-118688000	Flanking Active TSS	A549	lung
42	chr9:118687800-118688200	Enhancers	Placenta	Placenta
43	chr9:118687800-118692800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr9:118688000-118688200	Enhancers	A549	lung
45	chr9:118688000-118692000	Weak transcription	Hela-S3	cervix
46	chr9:118688200-118689000	Weak transcription	A549	lung
47	chr9:118688200-118692600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr9:118688200-118692600	Weak transcription	Placenta	Placenta
49	chr9:118689000-118690800	ZNF genes & repeats	A549	lung
50	chr9:118690800-118691200	Weak transcription	A549	lung

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