Variant report

Variant	esv2761538
Chromosome Location	chr9:86401015-86451943
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:443)
CpG islands
(count:305)
Chromatin interactive
region (count:15)
LncRNA
region (count:21)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:443 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr9:86432260-86432688	K562	blood:	n/a	chr9:86432477-86432493
2	BHLHE40	chr9:86432167-86432635	GM12878	blood:	n/a	chr9:86432477-86432493
3	BHLHE40	chr9:86432362-86432520	HepG2	liver:	n/a	chr9:86432477-86432493
4	CCNT2	chr9:86432252-86432698	K562	blood:	n/a	chr9:86432668-86432677
5	CEBPB	chr9:86434682-86434882	HepG2	liver:	n/a	chr9:86434732-86434743
6	CEBPB	chr9:86437426-86437435	HepG2	liver:	n/a	n/a
7	CEBPB	chr9:86403521-86403721	A549	lung:	n/a	n/a
8	CEBPB	chr9:86403534-86403759	HepG2	liver:	n/a	n/a
9	CEBPB	chr9:86434689-86434833	K562	blood:	n/a	chr9:86434732-86434743
10	CEBPB	chr9:86403491-86403742	IMR90	lung:	n/a	n/a
11	CEBPB	chr9:86427727-86427914	K562	blood:	n/a	n/a
12	CEBPB	chr9:86403542-86403557	H1-hESC	embryonic stem cell:	n/a	n/a
13	CHD1	chr9:86432239-86432282	GM12878	blood:	n/a	n/a
14	CHD1	chr9:86431789-86432598	IMR90	lung:	n/a	chr9:86432468-86432478 chr9:86431865-86431875
15	CHD2	chr9:86432265-86432364	GM12878	blood:	n/a	n/a
16	CHD2	chr9:86432810-86432972	GM12878	blood:	n/a	n/a
17	CHD2	chr9:86432754-86432816	Hela-S3	cervix:	n/a	n/a
18	CREB1	chr9:86432803-86432995	A549	lung:	n/a	n/a
19	CREB1	chr9:86432235-86433076	A549	lung:	n/a	n/a
20	CTCF	chr9:86432268-86432444	GM12891	blood:	n/a	n/a
21	CTCF	chr9:86432280-86432430	HBMEC	blood vessel:	n/a	n/a
22	CTCF	chr9:86445700-86445850	NHEK	skin:	n/a	n/a
23	CTCF	chr9:86432260-86432410	GM12869	blood:	n/a	n/a
24	CTCF	chr9:86432760-86432910	GM12873	blood:	n/a	n/a
25	CTCF	chr9:86445720-86445870	AG04450	lung:	n/a	n/a
26	CTCF	chr9:86433074-86433141	GM10248	blood:	n/a	n/a
27	CTCF	chr9:86432280-86432430	AG09319	gingival:	n/a	n/a
28	CTCF	chr9:86432240-86432390	GM12875	blood:	n/a	n/a
29	CTCF	chr9:86432244-86432464	GM19240	blood:	n/a	n/a
30	CTCF	chr9:86432220-86432370	AoAF	blood vessel:	n/a	n/a
31	CTCF	chr9:86432220-86432370	GM12869	blood:	n/a	n/a
32	CTCF	chr9:86427369-86427390	GM13976	blood:	n/a	n/a
33	CTCF	chr9:86432237-86432470	GM12892	blood:	n/a	n/a
34	CTCF	chr9:86445700-86445850	AoAF	blood vessel:	n/a	n/a
35	CTCF	chr9:86445700-86445850	BE2_C	brain:	n/a	n/a
36	CTCF	chr9:86445840-86445990	HCT-116	colon:	n/a	n/a
37	CTCF	chr9:86418254-86418306	MCF-7	breast:	n/a	n/a
38	CTCF	chr9:86432260-86432410	GM12872	blood:	n/a	n/a
39	CTCF	chr9:86432800-86432950	AG04449	skin:	n/a	n/a
40	CTCF	chr9:86432362-86432379	HepG2	liver:	n/a	n/a
41	CTCF	chr9:86432280-86432430	GM12870	blood:	n/a	n/a
42	CTCF	chr9:86432254-86432531	Fibrobl	skin:	n/a	n/a
43	CTCF	chr9:86432774-86432913	GM12878	blood:	n/a	n/a
44	CTCF	chr9:86432200-86432350	RPTEC	kidney:	n/a	n/a
45	CTCF	chr9:86432220-86432370	HCPEpiC	choroid plexus:	n/a	n/a
46	CTCF	chr9:86432260-86432410	HRPEpiC	eye:	n/a	n/a
47	CTCF	chr9:86445700-86445850	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr9:86432285-86432451	Gliobla	brain:	n/a	n/a
49	CTCF	chr9:86445680-86445830	HCPEpiC	choroid plexus:	n/a	n/a
50	CTCF	chr9:86432260-86432410	HCT-116	colon:	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	chr9:86432031-86432081	SK-N-MC	brain:	n/a
2	chr9:86432031-86432081	HCF	heart:	n/a
3	chr9:86432031-86432081	H1-hESC	embryonic stem cell:	embryo
4	chr9:86433081-86433131	AG04450	lung:	fetal
5	chr9:86432031-86432081	HAEpiC	amniotic membrane:	n/a
6	chr9:86433081-86433131	PFSK-1	brain:	n/a
7	chr9:86433764-86433814	AG09319	gingival:	n/a
8	chr9:86432854-86432904	ovcar-3	ovarian:	n/a
9	chr9:86432031-86432081	BJ	skin:	n/a
10	chr9:86431343-86431393	NHBE	bronchial:	n/a
11	chr9:86432031-86432081	MCF10A-Er-Src	breast:	n/a
12	chr9:86432031-86432081	HIPEpiC	eye:	n/a
13	chr9:86432854-86432904	MCF-7	breast:	n/a
14	chr9:86432031-86432081	SK-N-SH_RA	brain:	n/a
15	chr9:86431343-86431393	PrEC	prostate:	n/a
16	chr9:86433764-86433814	HRCEpiC	kidney:	n/a
17	chr9:86433764-86433814	Hepatocyte	liver:	n/a
18	chr9:86431343-86431393	BJ	skin:	n/a
19	chr9:86432854-86432904	H1-hESC	embryonic stem cell:	embryo
20	chr9:86433764-86433814	GM12878	blood:	n/a
21	chr9:86433764-86433814	ProgFib	skin:	n/a
22	chr9:86431343-86431393	HCF	heart:	n/a
23	chr9:86431343-86431393	GM12891	blood:	n/a
24	chr9:86432031-86432081	NB4	blood:	n/a
25	chr9:86433081-86433131	HL-60	blood:	n/a
26	chr9:86432854-86432904	GM12891	blood:	n/a
27	chr9:86433764-86433814	HIPEpiC	eye:	n/a
28	chr9:86432854-86432904	HRE	kidney:	n/a
29	chr9:86432854-86432904	MCF10A-Er-Src	breast:	n/a
30	chr9:86432031-86432081	T-47D	breast:	n/a
31	chr9:86432031-86432081	CMK	blood:	n/a
32	chr9:86433764-86433814	T-47D	breast:	n/a
33	chr9:86432031-86432081	GM12878	blood:	n/a
34	chr9:86431343-86431393	SKMC	muscle:	n/a
35	chr9:86433764-86433814	HPAEpiC	pulmonary alveolar:	n/a
36	chr9:86433764-86433814	Hela-S3	cervix:	n/a
37	chr9:86433081-86433131	LNCaP	prostate:	n/a
38	chr9:86433081-86433131	NB4	blood:	n/a
39	chr9:86432854-86432904	SK-N-SH_RA	brain:	n/a
40	chr9:86433764-86433814	GM12892	blood:	n/a
41	chr9:86431343-86431393	RPTEC	kidney:	n/a
42	chr9:86433081-86433131	ECC-1	luminal epithelium:	n/a
43	chr9:86432854-86432904	HEK293	kidney:	embryo
44	chr9:86433081-86433131	GM12892	blood:	n/a
45	chr9:86433081-86433131	MCF10A-Er-Src	breast:	n/a
46	chr9:86431343-86431393	SK-N-SH	brain:	n/a
47	chr9:86432854-86432904	HRPEpiC	eye:	n/a
48	chr9:86432854-86432904	Hepatocyte	liver:	n/a
49	chr9:86433081-86433131	Hepatocyte	liver:	n/a
50	chr9:86432031-86432081	HMEC	breast:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:86411947..86414043-chr9:86595098..86597695,2	MCF-7	breast:
2	chr9:86398629..86401211-chr9:86410405..86412819,2	MCF-7	breast:
3	chr9:86321607..86323730-chr9:86445405..86447358,2	MCF-7	breast:
4	chr9:86321555..86324208-chr9:86431445..86433817,2	MCF-7	breast:
5	chr9:86249075..86251124-chr9:86419195..86422058,2	K562	blood:
6	chr9:86321469..86324662-chr9:86431245..86433854,3	MCF-7	breast:
7	chr9:86402003..86404732-chr9:86411861..86414651,2	MCF-7	breast:
8	chr9:86430622..86432919-chr9:86535075..86537489,2	MCF-7	breast:
9	chr9:86236750..86239117-chr9:86447566..86449894,2	MCF-7	breast:
10	chr9:86429346..86431861-chr9:86535994..86537805,2	MCF-7	breast:
11	chr9:86322196..86324871-chr9:86423684..86425224,2	MCF-7	breast:
12	chr9:86321345..86324567-chr9:86398481..86402531,5	MCF-7	breast:
13	chr9:86320718..86323719-chr9:86450162..86455199,6	MCF-7	breast:
14	chr9:86394932..86396810-chr9:86405282..86407536,2	MCF-7	breast:
15	chr9:86398629..86401211-chr9:86410405..86412819,2	MCF-7	breast:

(count:21 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RMI1-6	chr9:86434721-86434785	NONHSAT132748
2	lnc-RMI1-5	chr9:86444571-86444630	ENSG00000226877.1
3	lnc-KIF27-1	chr9:86432900-86433036	NONHSAT132747
4	lnc-RMI1-6	chr9:86435226-86435354	ENSG00000245608
5	lnc-RMI1-6	chr9:86434446-86434617	NONHSAT132748
6	lnc-RMI1-6	chr9:86432881-86432983	ENSG00000245608
7	lnc-RMI1-6	chr9:86434446-86434617	ENSG00000245608
8	lnc-RMI1-6	chr9:86433316-86433488	ENSG00000245608
9	lnc-RMI1-5	chr9:86450466-86450620	ENSG00000226877.1
10	lnc-RMI1-6	chr9:86434721-86434785	ENSG00000245608
11	lnc-RMI1-6	chr9:86433316-86433488	NONHSAT132748
12	lnc-RMI1-5	chr9:86446478-86446527	ENSG00000226877.3
13	lnc-RMI1-5	chr9:86445783-86445854	ENSG00000226877.1
14	lnc-RMI1-5	chr9:86446480-86446527	ENSG00000226877.1
15	lnc-RMI1-6	chr9:86442823-86443087	ENSG00000245608
16	lnc-RMI1-6	chr9:86432881-86432983	NONHSAT132748
17	lnc-RMI1-5	chr9:86446475-86446527	ENSG00000226877.1
18	lnc-RMI1-5	chr9:86446478-86446527	ENSG00000226877.1
19	lnc-KIF27-1	chr9:86431911-86432042	NONHSAT132747
20	lnc-RMI1-6	chr9:86435226-86435354	NONHSAT132748
21	lnc-RMI1-6	chr9:86442823-86443094	NONHSAT132748

No data

Variant related genes	Relation type
ENSG00000226877	TF binding region
ENSG00000231616	TF binding region
GKAP1	TF binding region
ENSG00000226877	CpG island
ENSG00000231616	CpG island
GKAP1	CpG island
ENSG00000148057	chromatin interactions
ENSG00000178966	chromatin interactions
ENSG00000135018	chromatin interactions
ENSG00000165113	chromatin interactions
ENSG00000165119	chromatin interactions
ENSG00000165115	chromatin interactions
ENSG00000254473	chromatin interactions
FAM49B	miRNA target sites
RUNX1	miRNA target sites
PDS5B	miRNA target sites
RNF182	miRNA target sites

Extended variants
information (count: 1660 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:1660 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs140962189	chr9:86401060-86401061	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs539382281	chr9:86401070-86401071	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs376443307	chr9:86401077-86401078	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs11792634	chr9:86401099-86401100	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs570545030	chr9:86401117-86401118	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs35479440	chr9:86401161-86401162	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs539460604	chr9:86401167-86401168	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs376418782	chr9:86401183-86401184	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs371479849	chr9:86401184-86401185	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs546633299	chr9:86401229-86401230	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs374965379	chr9:86401232-86401233	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs11792650	chr9:86401242-86401243	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs538603458	chr9:86401249-86401250	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs557046363	chr9:86401273-86401274	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs570039447	chr9:86401318-86401319	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs536473651	chr9:86401338-86401339	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs554449215	chr9:86401349-86401350	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs142020790	chr9:86401363-86401364	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs540529650	chr9:86401380-86401381	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs558842742	chr9:86401391-86401392	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs11140249	chr9:86401404-86401405	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs184958099	chr9:86401410-86401411	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs116985359	chr9:86401413-86401414	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs529732987	chr9:86401434-86401435	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs543241919	chr9:86401442-86401443	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs373542500	chr9:86401444-86401445	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs78205969	chr9:86401456-86401457	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs79892290	chr9:86401457-86401458	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs528809091	chr9:86401472-86401473	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs546894548	chr9:86401482-86401483	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs189803767	chr9:86401551-86401552	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs6559742	chr9:86401611-86401612	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs550536605	chr9:86401630-86401631	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs181050777	chr9:86401651-86401652	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs75963769	chr9:86401661-86401662	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs563578451	chr9:86401673-86401674	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs112404763	chr9:86401674-86401675	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs564358232	chr9:86401735-86401736	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs552627239	chr9:86401737-86401738	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs77901069	chr9:86401753-86401754	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs11140250	chr9:86401778-86401779	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs574516457	chr9:86401800-86401801	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs541559026	chr9:86401812-86401813	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs560148034	chr9:86401850-86401851	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs528674193	chr9:86401851-86401852	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs540396572	chr9:86401864-86401865	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs138390108	chr9:86401907-86401908	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs560009393	chr9:86401945-86401946	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs201615366	chr9:86401952-86401953	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs528667199	chr9:86401975-86401976	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Chordoma	18071362	CNVD
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
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	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
Leukemia	18688285	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
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Bipolar disorder	18458673	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Urothelial cell carcinoma	18451213	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Renal cell carcinoma	18765545	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:565 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:86348400-86415400	Weak transcription	Fetal Heart	heart
2	chr9:86350000-86431600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr9:86350800-86407000	Weak transcription	Primary B cells from cord blood	blood
4	chr9:86352000-86411800	Weak transcription	Ovary	ovary
5	chr9:86353000-86432000	Weak transcription	Lung	lung
6	chr9:86363800-86412400	Weak transcription	HepG2	liver
7	chr9:86363800-86431200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
8	chr9:86364800-86412000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
9	chr9:86364800-86413400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
10	chr9:86367000-86413600	Weak transcription	Rectal Mucosa Donor 29	rectum
11	chr9:86367400-86411800	Weak transcription	Brain Substantia Nigra	brain
12	chr9:86367600-86412000	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr9:86373200-86411800	Weak transcription	Stomach Smooth Muscle	stomach
14	chr9:86377000-86412600	Weak transcription	Brain Anterior Caudate	brain
15	chr9:86377200-86432000	Weak transcription	Gastric	stomach
16	chr9:86378400-86418400	Weak transcription	Pancreatic Islets	Pancreatic Islet
17	chr9:86380200-86431600	Weak transcription	Fetal Kidney	kidney
18	chr9:86381400-86411800	Weak transcription	Brain Hippocampus Middle	brain
19	chr9:86383600-86425800	Weak transcription	Sigmoid Colon	Sigmoid Colon
20	chr9:86385400-86409200	Weak transcription	Primary T cells from cord blood	blood
21	chr9:86388200-86411400	Weak transcription	Fetal Muscle Trunk	muscle
22	chr9:86389000-86431600	Weak transcription	Rectal Smooth Muscle	rectum
23	chr9:86391800-86411800	Weak transcription	Rectal Mucosa Donor 31	rectum
24	chr9:86392000-86431600	Weak transcription	Psoas Muscle	Psoas
25	chr9:86392000-86431800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr9:86393400-86412000	Weak transcription	Brain Angular Gyrus	brain
27	chr9:86393600-86412400	Weak transcription	Brain Inferior Temporal Lobe	brain
28	chr9:86394400-86431600	Weak transcription	Colon Smooth Muscle	Colon
29	chr9:86394800-86412600	Weak transcription	Primary T helper cells PMA-I stimulated	--
30	chr9:86395000-86416400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
31	chr9:86395600-86417400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr9:86396600-86403400	Weak transcription	HUES48 Cell Line	embryonic stem cell
33	chr9:86397000-86402400	Strong transcription	Liver	Liver
34	chr9:86397000-86420000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr9:86397400-86412200	Weak transcription	Primary T cells fromperipheralblood	blood
36	chr9:86397400-86413400	Weak transcription	Primary B cells from peripheral blood	blood
37	chr9:86397400-86415600	Weak transcription	Brain Germinal Matrix	brain
38	chr9:86397400-86419400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
39	chr9:86397400-86423400	Weak transcription	HUES64 Cell Line	embryonic stem cell
40	chr9:86397800-86401200	Strong transcription	Primary hematopoietic stem cells	blood
41	chr9:86398200-86401200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
42	chr9:86398600-86402200	Weak transcription	Fetal Brain Female	brain
43	chr9:86399000-86431000	Weak transcription	A549	lung
44	chr9:86399400-86408800	Weak transcription	Fetal Intestine Small	intestine
45	chr9:86399400-86408800	Weak transcription	Left Ventricle	heart
46	chr9:86399400-86409600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
47	chr9:86399400-86411400	Weak transcription	Aorta	Aorta
48	chr9:86399400-86411800	Weak transcription	Primary T helper cells fromperipheralblood	blood
49	chr9:86399400-86412000	Weak transcription	Duodenum Mucosa	Duodenum
50	chr9:86399400-86412200	Weak transcription	Fetal Muscle Leg	muscle

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