Variant report

Variant	nsv6774
Chromosome Location	chr9:140680758-140725053
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:582)
CpG islands
(count:1405)
Chromatin interactive
region (count:24)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:582 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr9:140710777-140711402	GM12878	blood:	n/a	n/a
2	ATF2	chr9:140703449-140703804	GM12878	blood:	n/a	n/a
3	ATF2	chr9:140710782-140711539	GM12878	blood:	n/a	n/a
4	BATF	chr9:140710900-140711326	GM12878	blood:	n/a	chr9:140711120-140711131
5	BATF	chr9:140710702-140711592	GM12878	blood:	n/a	chr9:140711120-140711131
6	BCL11A	chr9:140710826-140711435	GM12878	blood:	n/a	n/a
7	BCL11A	chr9:140703488-140703846	GM12878	blood:	n/a	n/a
8	BCL11A	chr9:140720112-140720348	GM12878	blood:	n/a	chr9:140720260-140720269
9	BCL3	chr9:140707638-140708059	GM12878	blood:	n/a	n/a
10	BCL3	chr9:140699230-140700056	GM12878	blood:	n/a	n/a
11	BCL3	chr9:140702187-140702477	GM12878	blood:	n/a	n/a
12	BCL3	chr9:140707704-140708126	GM12878	blood:	n/a	n/a
13	BCL3	chr9:140699190-140700049	GM12878	blood:	n/a	n/a
14	BCLAF1	chr9:140710805-140711566	GM12878	blood:	n/a	n/a
15	BCLAF1	chr9:140703525-140703782	GM12878	blood:	n/a	n/a
16	BCLAF1	chr9:140703419-140703881	GM12878	blood:	n/a	n/a
17	BHLHE40	chr9:140683842-140684270	HepG2	liver:	n/a	n/a
18	BHLHE40	chr9:140710980-140711476	GM12878	blood:	n/a	n/a
19	BHLHE40	chr9:140720100-140720383	GM12878	blood:	n/a	n/a
20	CEBPB	chr9:140681002-140681220	IMR90	lung:	n/a	n/a
21	CEBPB	chr9:140684103-140684275	HepG2	liver:	n/a	chr9:140684237-140684248
22	CEBPB	chr9:140684121-140684398	HepG2	liver:	n/a	chr9:140684237-140684248
23	CEBPB	chr9:140710730-140711472	GM12878	blood:	n/a	n/a
24	CHD2	chr9:140699464-140699664	GM12878	blood:	n/a	n/a
25	CHD2	chr9:140711231-140711386	GM12878	blood:	n/a	n/a
26	CHD2	chr9:140720163-140720400	GM12878	blood:	n/a	n/a
27	CREB1	chr9:140720000-140720455	GM12878	blood:	n/a	n/a
28	CREB1	chr9:140710882-140711564	GM12878	blood:	n/a	n/a
29	CTCF	chr9:140710100-140710250	GM12866	blood:	n/a	n/a
30	CTCF	chr9:140711501-140711544	GM12891	blood:	n/a	n/a
31	CTCF	chr9:140711380-140711530	GM12871	blood:	n/a	n/a
32	CTCF	chr9:140699442-140699492	MCF-7	breast:	n/a	n/a
33	CTCF	chr9:140708886-140708972	NHEK	skin:	n/a	n/a
34	CTCF	chr9:140711474-140711578	GM19238	blood:	n/a	n/a
35	CTCF	chr9:140707811-140707840	MCF-7	breast:	n/a	n/a
36	CTCF	chr9:140711464-140711581	GM13977	blood:	n/a	n/a
37	CTCF	chr9:140711486-140711537	GM19240	blood:	n/a	n/a
38	CTCF	chr9:140711340-140711490	GM12875	blood:	n/a	n/a
39	CTCF	chr9:140711500-140711650	GM12872	blood:	n/a	n/a
40	EBF1	chr9:140703609-140703811	GM12878	blood:	n/a	n/a
41	EBF1	chr9:140720157-140720348	GM12878	blood:	n/a	n/a
42	EBF1	chr9:140711058-140711601	GM12878	blood:	n/a	n/a
43	EBF1	chr9:140711056-140711573	GM12878	blood:	n/a	n/a
44	EBF1	chr9:140703695-140703873	GM12878	blood:	n/a	chr9:140703808-140703819
45	EBF1	chr9:140720105-140720414	GM12878	blood:	n/a	n/a
46	EBF1	chr9:140703663-140703934	GM12878	blood:	n/a	chr9:140703808-140703819
47	EBF1	chr9:140710885-140711668	GM12878	blood:	n/a	n/a
48	EGR1	chr9:140697373-140697549	K562	blood:	n/a	n/a
49	ELF1	chr9:140683924-140684174	HepG2	liver:	n/a	n/a
50	ELF1	chr9:140710863-140711566	GM12878	blood:	n/a	n/a

(count:1405 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:140683212-140683262	HCT-116	colon:	n/a
2	chr9:140683797-140683847	HUVEC	blood vessel:	n/a
3	chr9:140683212-140683262	HCT-116	colon:	n/a
4	chr9:140683797-140683847	HUVEC	blood vessel:	n/a
5	chr9:140712932-140712982	HCT-116	colon:	n/a
6	chr9:140707378-140707428	Caco-2	colon:	n/a
7	chr9:140683527-140683577	HCT-116	colon:	n/a
8	chr9:140704398-140704448	NHDF-neo	bronchial:	n/a
9	chr9:140681206-140681256	HCT-116	colon:	n/a
10	chr9:140715062-140715112	HNPCEpiC	eye:	n/a
11	chr9:140707378-140707428	GM06990	blood:	n/a
12	chr9:140708214-140708264	HL-60	blood:	n/a
13	chr9:140681206-140681256	AG09309	skin:	n/a
14	chr9:140716770-140716820	SK-N-SH_RA	brain:	n/a
15	chr9:140683212-140683262	HRCEpiC	kidney:	n/a
16	chr9:140687144-140687194	Jurkat	blood:	n/a
17	chr9:140683649-140683699	MCF-7	breast:	n/a
18	chr9:140705990-140706040	HAEpiC	amniotic membrane:	n/a
19	chr9:140708214-140708264	HepG2	liver:	n/a
20	chr9:140683797-140683847	NB4	blood:	n/a
21	chr9:140715062-140715112	PFSK-1	brain:	n/a
22	chr9:140709558-140709608	AG09319	gingival:	n/a
23	chr9:140681131-140681181	ovcar-3	ovarian:	n/a
24	chr9:140684842-140684892	H1-hESC	embryonic stem cell:	embryo
25	chr9:140704065-140704115	Caco-2	colon:	n/a
26	chr9:140683797-140683847	NHBE	bronchial:	n/a
27	chr9:140714075-140714125	NH-A	brain:	n/a
28	chr9:140704763-140704813	MCF10A-Er-Src	breast:	n/a
29	chr9:140705990-140706040	HIPEpiC	eye:	n/a
30	chr9:140705990-140706040	HPAEpiC	pulmonary alveolar:	n/a
31	chr9:140709558-140709608	HRPEpiC	eye:	n/a
32	chr9:140708214-140708264	PrEC	prostate:	n/a
33	chr9:140711975-140712025	ovcar-3	ovarian:	n/a
34	chr9:140704763-140704813	ovcar-3	ovarian:	n/a
35	chr9:140681131-140681181	HCPEpiC	choroid plexus:	n/a
36	chr9:140681131-140681181	SAEC	small airway:	n/a
37	chr9:140705990-140706040	HCPEpiC	choroid plexus:	n/a
38	chr9:140684842-140684892	HRPEpiC	eye:	n/a
39	chr9:140716770-140716820	SAEC	small airway:	n/a
40	chr9:140714075-140714125	GM12878	blood:	n/a
41	chr9:140683212-140683262	Hepatocyte	liver:	n/a
42	chr9:140683797-140683847	BE2_C	brain:	n/a
43	chr9:140704065-140704115	Jurkat	blood:	n/a
44	chr9:140704398-140704448	HCF	heart:	n/a
45	chr9:140715062-140715112	NHBE	bronchial:	n/a
46	chr9:140714075-140714125	Hepatocyte	liver:	n/a
47	chr9:140716770-140716820	AG04450	lung:	fetal
48	chr9:140681131-140681181	SKMC	muscle:	n/a
49	chr9:140684842-140684892	NH-A	brain:	n/a
50	chr9:140716770-140716820	HAEpiC	amniotic membrane:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:140700744..140703518-chr9:140712352..140715179,2	K562	blood:
2	chr9:140720128..140722152-chr9:140723312..140725717,2	K562	blood:
3	chr9:140699377..140703481-chr9:140712801..140716368,4	K562	blood:
4	chr9:140720745..140725244-chr9:140725368..140729857,4	K562	blood:
5	chr9:140679440..140682132-chr9:140702994..140705523,2	K562	blood:
6	chr9:140701752..140704462-chr9:140707799..140711263,3	MCF-7	breast:
7	chr9:140706148..140707731-chr9:140712808..140715644,2	K562	blood:
8	chr9:140692420..140694081-chr9:140698871..140701591,2	K562	blood:
9	chr9:140699377..140703481-chr9:140712801..140716368,4	K562	blood:
10	chr9:140706148..140709058-chr9:140712432..140716292,4	K562	blood:
11	chr9:140720128..140722152-chr9:140723312..140725717,2	K562	blood:
12	chr9:140692420..140694081-chr9:140698871..140701591,2	K562	blood:
13	chr9:140700744..140703518-chr9:140712352..140715179,2	K562	blood:
14	chr9:140713786..140716725-chr9:140719882..140722951,3	K562	blood:
15	chr9:140689938..140692282-chr9:140694934..140697761,2	MCF-7	breast:
16	chr9:140718370..140720341-chr9:140724405..140727123,2	MCF-7	breast:
17	chr9:140700980..140705198-chr9:140707876..140710677,3	K562	blood:
18	chr9:140672962..140675618-chr9:140678748..140680768,2	K562	blood:
19	chr9:140713786..140716725-chr9:140719882..140722951,3	K562	blood:
20	chr9:140722366..140725361-chr9:140730961..140733725,2	MCF-7	breast:
21	chr9:140706148..140707731-chr9:140712808..140715644,2	K562	blood:
22	chr9:140689938..140692282-chr9:140694934..140697761,2	MCF-7	breast:
23	chr9:140679440..140682132-chr9:140702994..140705523,2	K562	blood:
24	chr9:140705835..140707524-chr9:140709188..140711003,2	K562	blood:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL772363.1-5	chr9:140682117-140683139	NONHSAT135752
2	lnc-AL772363.1-4	chr9:140703295-140703875	NONHSAT135753

No data

Variant related genes	Relation type
EHMT1	TF binding region
ENSG00000255585	TF binding region
EHMT1	CpG island
ENSG00000255585	CpG island
ENSG00000207693	chromatin interactions
ENSG00000181090	chromatin interactions

Extended variants
information (count: 2216 )
Associated
traits (count: 20 )

Variant overlapped rSNPs/rCNVs (count:2216 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs144334747	chr9:140680764-140680765	Genic enhancers Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs7858355	chr9:140680789-140680790	Genic enhancers Enhancers Strong transcription Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs542808541	chr9:140680825-140680826	Genic enhancers Enhancers Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs532167757	chr9:140680904-140680905	Genic enhancers Enhancers Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs551842410	chr9:140680913-140680914	Genic enhancers Enhancers Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs559408966	chr9:140680978-140680979	Genic enhancers Enhancers Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs73669179	chr9:140680985-140680986	Genic enhancers Enhancers Strong transcription Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs182585331	chr9:140681011-140681012	Genic enhancers Enhancers Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs141445710	chr9:140681021-140681022	Genic enhancers Enhancers Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs150831094	chr9:140681031-140681032	Genic enhancers Enhancers Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs548392108	chr9:140681032-140681033	Genic enhancers Enhancers Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs186836651	chr9:140681034-140681035	Genic enhancers Enhancers Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs533701770	chr9:140681035-140681036	Genic enhancers Enhancers Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs191667938	chr9:140681087-140681088	Genic enhancers Enhancers Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs73578105	chr9:140681088-140681089	Genic enhancers Enhancers Strong transcription Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs539454634	chr9:140681103-140681104	Genic enhancers Enhancers Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs556276489	chr9:140681104-140681105	Genic enhancers Enhancers Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs139903405	chr9:140681131-140681132	Genic enhancers Enhancers Strong transcription Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
19	rs375807547	chr9:140681156-140681157	Genic enhancers Enhancers Strong transcription Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
20	rs370134742	chr9:140681180-140681181	Genic enhancers Enhancers Strong transcription Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
21	rs572694109	chr9:140681197-140681198	Genic enhancers Enhancers Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs541612303	chr9:140681206-140681207	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
23	rs184639344	chr9:140681244-140681245	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
24	rs373099152	chr9:140681257-140681258	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs116638775	chr9:140681283-140681284	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs551122653	chr9:140681286-140681287	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs564884971	chr9:140681308-140681309	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs145342928	chr9:140681359-140681360	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs73578107	chr9:140681360-140681361	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs531666221	chr9:140681382-140681383	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs543997664	chr9:140681391-140681392	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs187544954	chr9:140681409-140681410	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs561617715	chr9:140681460-140681461	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs527484467	chr9:140681521-140681522	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs547147125	chr9:140681532-140681533	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs563788126	chr9:140681598-140681599	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs553475368	chr9:140681617-140681618	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs539549210	chr9:140681624-140681625	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs530563946	chr9:140681639-140681640	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs201649287	chr9:140681664-140681665	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs80265092	chr9:140681674-140681675	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs147861778	chr9:140681697-140681698	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs550272564	chr9:140681706-140681707	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs113475692	chr9:140681710-140681711	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs572732254	chr9:140681743-140681744	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs535242598	chr9:140681761-140681762	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs532853825	chr9:140681776-140681777	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs117982614	chr9:140681805-140681806	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs549535775	chr9:140681806-140681807	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs565467784	chr9:140681816-140681817	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:20)

Disease	PMID	Source
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Cardiac fibroma	18329553	CNVD
Lung cancer	19147751	CNVD
Cervical cancer	17311676	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Chordoma	18071362	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Sudden cardiac death	19188705	CNVD
Myoepithelioma	18604193	CNVD
Tuberous sclerosis	19566914	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Mantle cell lymphoma	19029149	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:1757 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:140649800-140712400	Weak transcription	Psoas Muscle	Psoas
2	chr9:140650200-140682600	Strong transcription	Monocytes-CD14+_RO01746	blood
3	chr9:140650200-140700000	Strong transcription	Primary T cells from cord blood	blood
4	chr9:140659000-140683600	Strong transcription	Liver	Liver
5	chr9:140663800-140682000	Strong transcription	Rectal Mucosa Donor 29	rectum
6	chr9:140663800-140683000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
7	chr9:140664000-140683000	Strong transcription	Stomach Smooth Muscle	stomach
8	chr9:140664200-140681000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
9	chr9:140664200-140682600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr9:140664200-140698600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
11	chr9:140664200-140701000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr9:140664600-140708000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr9:140664800-140700000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr9:140665000-140681600	Strong transcription	Primary hematopoietic stem cells	blood
15	chr9:140665000-140700000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr9:140665200-140702000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr9:140665400-140682800	Strong transcription	Fetal Intestine Small	intestine
18	chr9:140665400-140697800	Strong transcription	Thymus	Thymus
19	chr9:140665400-140700800	Strong transcription	Fetal Stomach	stomach
20	chr9:140666200-140682200	Strong transcription	Lung	lung
21	chr9:140666600-140682000	Strong transcription	Duodenum Mucosa	Duodenum
22	chr9:140667200-140698000	Strong transcription	Dnd41	blood
23	chr9:140667200-140699000	Strong transcription	Primary neutrophils fromperipheralblood	blood
24	chr9:140668200-140698000	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
25	chr9:140668200-140699000	Strong transcription	Esophagus	oesophagus
26	chr9:140668200-140700000	Strong transcription	Fetal Brain Female	brain
27	chr9:140668400-140681800	Strong transcription	Spleen	Spleen
28	chr9:140669600-140683200	Strong transcription	Skeletal Muscle Male	skeletal muscle
29	chr9:140673200-140685000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
30	chr9:140675000-140689800	Weak transcription	Fetal Brain Male	brain
31	chr9:140675600-140681200	Strong transcription	Muscle Satellite Cultured Cells	--
32	chr9:140675600-140681400	Strong transcription	Primary monocytes fromperipheralblood	blood
33	chr9:140675600-140682000	Strong transcription	Primary T helper cells fromperipheralblood	blood
34	chr9:140675600-140682000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
35	chr9:140675600-140682000	Strong transcription	Sigmoid Colon	Sigmoid Colon
36	chr9:140675600-140682600	Strong transcription	Fetal Intestine Large	intestine
37	chr9:140675600-140683400	Strong transcription	Primary B cells from peripheral blood	blood
38	chr9:140675600-140690800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr9:140675600-140698600	Strong transcription	Placenta	Placenta
40	chr9:140675800-140682600	Strong transcription	GM12878-XiMat	blood
41	chr9:140675800-140682800	Strong transcription	Right Ventricle	heart
42	chr9:140675800-140685800	Strong transcription	Fetal Thymus	thymus
43	chr9:140675800-140688400	Strong transcription	Brain Germinal Matrix	brain
44	chr9:140675800-140695600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
45	chr9:140676000-140681200	Strong transcription	Hela-S3	cervix
46	chr9:140676000-140681800	Strong transcription	Primary T cells fromperipheralblood	blood
47	chr9:140676000-140690800	Strong transcription	Primary T helper cells PMA-I stimulated	--
48	chr9:140676400-140681800	Strong transcription	Colonic Mucosa	Colon
49	chr9:140676400-140699400	Weak transcription	Fetal Heart	heart
50	chr9:140677400-140689400	Weak transcription	Pancreatic Islets	Pancreatic Islet

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