Variant report

Variant	nsv1052590
Chromosome Location	chr9:140689236-140766891
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr9:140703449-140703804	GM12878	blood:	n/a	n/a
2	ATF2	chr9:140761215-140761514	GM12878	blood:	n/a	n/a
3	ATF2	chr9:140710777-140711402	GM12878	blood:	n/a	n/a
4	ATF2	chr9:140710782-140711539	GM12878	blood:	n/a	n/a
5	BATF	chr9:140761031-140761428	GM12878	blood:	n/a	n/a
6	BATF	chr9:140710900-140711326	GM12878	blood:	n/a	chr9:140711120-140711131
7	BATF	chr9:140710702-140711592	GM12878	blood:	n/a	chr9:140711120-140711131
8	BATF	chr9:140731105-140731321	GM12878	blood:	n/a	n/a
9	BATF	chr9:140747930-140748125	GM12878	blood:	n/a	n/a
10	BCL11A	chr9:140703488-140703846	GM12878	blood:	n/a	n/a
11	BCL11A	chr9:140720112-140720348	GM12878	blood:	n/a	chr9:140720260-140720269
12	BCL11A	chr9:140710826-140711435	GM12878	blood:	n/a	n/a
13	BCL11A	chr9:140761035-140761355	GM12878	blood:	n/a	n/a
14	BCL3	chr9:140699230-140700056	GM12878	blood:	n/a	n/a
15	BCL3	chr9:140699190-140700049	GM12878	blood:	n/a	n/a
16	BCL3	chr9:140702187-140702477	GM12878	blood:	n/a	n/a
17	BCL3	chr9:140707704-140708126	GM12878	blood:	n/a	n/a
18	BCL3	chr9:140707638-140708059	GM12878	blood:	n/a	n/a
19	BCL3	chr9:140760724-140761478	GM12878	blood:	n/a	n/a
20	BCLAF1	chr9:140703419-140703881	GM12878	blood:	n/a	n/a
21	BCLAF1	chr9:140703525-140703782	GM12878	blood:	n/a	n/a
22	BCLAF1	chr9:140710805-140711566	GM12878	blood:	n/a	n/a
23	BHLHE40	chr9:140720100-140720383	GM12878	blood:	n/a	n/a
24	BHLHE40	chr9:140710980-140711476	GM12878	blood:	n/a	n/a
25	BHLHE40	chr9:140731130-140731329	K562	blood:	n/a	n/a
26	BHLHE40	chr9:140761159-140761359	GM12878	blood:	n/a	n/a
27	BHLHE40	chr9:140760778-140760955	GM12878	blood:	n/a	n/a
28	BRCA1	chr9:140761625-140761775	GM12878	blood:	n/a	n/a
29	CCNT2	chr9:140729504-140729518	K562	blood:	n/a	n/a
30	CEBPB	chr9:140746423-140746547	A549	lung:	n/a	n/a
31	CEBPB	chr9:140761024-140761478	GM12878	blood:	n/a	n/a
32	CEBPB	chr9:140733435-140733667	HepG2	liver:	n/a	chr9:140733512-140733523 chr9:140733514-140733523 chr9:140733513-140733524
33	CEBPB	chr9:140731077-140731484	Hela-S3	cervix:	n/a	chr9:140731272-140731281 chr9:140731270-140731283 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731270-140731281
34	CEBPB	chr9:140731088-140731472	A549	lung:	n/a	chr9:140731272-140731281 chr9:140731270-140731283 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731270-140731281
35	CEBPB	chr9:140731067-140731469	HepG2	liver:	n/a	chr9:140731272-140731281 chr9:140731270-140731283 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731270-140731281
36	CEBPB	chr9:140731131-140731378	K562	blood:	n/a	chr9:140731272-140731281 chr9:140731270-140731283 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731270-140731281
37	CEBPB	chr9:140746402-140746765	MCF-7	breast:	n/a	n/a
38	CEBPB	chr9:140731082-140731475	H1-hESC	embryonic stem cell:	n/a	chr9:140731272-140731281 chr9:140731270-140731283 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731270-140731281
39	CEBPB	chr9:140733389-140733674	IMR90	lung:	n/a	chr9:140733512-140733523 chr9:140733514-140733523 chr9:140733513-140733524
40	CEBPB	chr9:140731077-140731543	K562	blood:	n/a	chr9:140731272-140731281 chr9:140731270-140731283 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731270-140731281
41	CEBPB	chr9:140733435-140733635	A549	lung:	n/a	chr9:140733512-140733523 chr9:140733514-140733523 chr9:140733513-140733524
42	CEBPB	chr9:140731101-140731454	HepG2	liver:	n/a	chr9:140731272-140731281 chr9:140731270-140731283 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731270-140731281
43	CEBPB	chr9:140731082-140731461	IMR90	lung:	n/a	chr9:140731272-140731281 chr9:140731270-140731283 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731270-140731281
44	CEBPB	chr9:140731027-140731466	K562	blood:	n/a	chr9:140731272-140731281 chr9:140731270-140731283 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731270-140731281
45	CEBPB	chr9:140731058-140731398	HepG2	liver:	n/a	chr9:140731272-140731281 chr9:140731270-140731283 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731270-140731281
46	CEBPB	chr9:140730916-140731619	A549	lung:	n/a	chr9:140731272-140731281 chr9:140731270-140731283 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731270-140731281
47	CEBPB	chr9:140745962-140746844	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr9:140731134-140731426	ECC-1	luminal epithelium:	n/a	chr9:140731272-140731281 chr9:140731270-140731283 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731270-140731281
49	CEBPB	chr9:140710730-140711472	GM12878	blood:	n/a	n/a
50	CEBPB	chr9:140730983-140731575	MCF-7	breast:	n/a	chr9:140731272-140731281 chr9:140731270-140731283 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731270-140731281

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:140704763-140704813	IMR90	lung:	fetal
2	chr9:140709033-140709083	SK-N-SH	brain:	n/a
3	chr9:140703588-140703638	ECC-1	luminal epithelium:	n/a
4	chr9:140704763-140704813	IMR90	lung:	fetal
5	chr9:140709033-140709083	SK-N-SH	brain:	n/a
6	chr9:140703588-140703638	ECC-1	luminal epithelium:	n/a
7	chr9:140709558-140709608	HRCEpiC	kidney:	n/a
8	chr9:140731022-140731072	GM06990	blood:	n/a
9	chr9:140731445-140731495	K562	blood:	n/a
10	chr9:140715062-140715112	HL-60	blood:	n/a
11	chr9:140709033-140709083	HPAEpiC	pulmonary alveolar:	n/a
12	chr9:140733714-140733764	HEEpiC	esophagus:	n/a
13	chr9:140704398-140704448	NHBE	bronchial:	n/a
14	chr9:140731022-140731072	HCF	heart:	n/a
15	chr9:140726863-140726913	BE2_C	brain:	n/a
16	chr9:140715062-140715112	HMEC	breast:	n/a
17	chr9:140704065-140704115	GM12878	blood:	n/a
18	chr9:140725587-140725637	HUVEC	blood vessel:	n/a
19	chr9:140729712-140729762	AG04450	lung:	fetal
20	chr9:140729712-140729762	HRCEpiC	kidney:	n/a
21	chr9:140714075-140714125	HUVEC	blood vessel:	n/a
22	chr9:140727297-140727347	SKMC	muscle:	n/a
23	chr9:140735058-140735108	AoSMC	blood vessel:	n/a
24	chr9:140731445-140731495	HUVEC	blood vessel:	n/a
25	chr9:140727297-140727347	GM12891	blood:	n/a
26	chr9:140730317-140730367	AG04449	skin:	fetal
27	chr9:140726863-140726913	HCF	heart:	n/a
28	chr9:140703588-140703638	MCF10A-Er-Src	breast:	n/a
29	chr9:140726863-140726913	GM12891	blood:	n/a
30	chr9:140709033-140709083	GM12878	blood:	n/a
31	chr9:140727571-140727621	U87	brain:	n/a
32	chr9:140703637-140703687	HAEpiC	amniotic membrane:	n/a
33	chr9:140705990-140706040	ProgFib	skin:	n/a
34	chr9:140728491-140728541	AG09309	skin:	n/a
35	chr9:140708214-140708264	HEEpiC	esophagus:	n/a
36	chr9:140730806-140730856	AG10803	skin:	n/a
37	chr9:140709558-140709608	HAEpiC	amniotic membrane:	n/a
38	chr9:140729241-140729291	H1-hESC	embryonic stem cell:	embryo
39	chr9:140716770-140716820	RPTEC	kidney:	n/a
40	chr9:140703588-140703638	AG04450	lung:	fetal
41	chr9:140703588-140703638	BE2_C	brain:	n/a
42	chr9:140725587-140725637	BJ	skin:	n/a
43	chr9:140729712-140729762	NHDF-neo	bronchial:	n/a
44	chr9:140709033-140709083	NHBE	bronchial:	n/a
45	chr9:140728301-140728351	A549	lung:	n/a
46	chr9:140709558-140709608	PFSK-1	brain:	n/a
47	chr9:140704763-140704813	HRPEpiC	eye:	n/a
48	chr9:140730806-140730856	ovcar-3	ovarian:	n/a
49	chr9:140709558-140709608	NT2-D1	testis:	n/a
50	chr9:140703588-140703638	U87	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:140706148..140709058-chr9:140712432..140716292,4	K562	blood:
2	chr9:140706148..140707731-chr9:140712808..140715644,2	K562	blood:
3	chr9:140689938..140692282-chr9:140694934..140697761,2	MCF-7	breast:
4	chr9:140732797..140735433-chr9:140735710..140738705,2	MCF-7	breast:
5	chr9:140725074..140728358-chr9:140730980..140733506,3	K562	blood:
6	chr9:140763820..140766702-chr9:140806866..140808617,2	K562	blood:
7	chr9:140720745..140725244-chr9:140725368..140729857,4	K562	blood:
8	chr9:140699377..140703481-chr9:140712801..140716368,4	K562	blood:
9	chr9:140705835..140707524-chr9:140709188..140711003,2	K562	blood:
10	chr9:140713786..140716725-chr9:140719882..140722951,3	K562	blood:
11	chr9:140706148..140707731-chr9:140712808..140715644,2	K562	blood:
12	chr9:140699377..140703481-chr9:140712801..140716368,4	K562	blood:
13	chr9:140725074..140728358-chr9:140730980..140733506,3	K562	blood:
14	chr9:140713786..140716725-chr9:140719882..140722951,3	K562	blood:
15	chr9:140701752..140704462-chr9:140707799..140711263,3	MCF-7	breast:
16	chr9:140720128..140722152-chr9:140723312..140725717,2	K562	blood:
17	chr9:140692420..140694081-chr9:140698871..140701591,2	K562	blood:
18	chr9:140722366..140725361-chr9:140730961..140733725,2	MCF-7	breast:
19	chr9:140689938..140692282-chr9:140694934..140697761,2	MCF-7	breast:
20	chr9:140700744..140703518-chr9:140712352..140715179,2	K562	blood:
21	chr9:140720128..140722152-chr9:140723312..140725717,2	K562	blood:
22	chr9:140718370..140720341-chr9:140724405..140727123,2	MCF-7	breast:
23	chr9:140700744..140703518-chr9:140712352..140715179,2	K562	blood:
24	chr9:140692420..140694081-chr9:140698871..140701591,2	K562	blood:
25	chr9:140679440..140682132-chr9:140702994..140705523,2	K562	blood:
26	chr9:140700980..140705198-chr9:140707876..140710677,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL772363.1-1	chr9:140762379-140762689	ENSG00000203987.2
2	lnc-AL772363.1-4	chr9:140703295-140703875	NONHSAT135753
3	lnc-AL772363.1-1	chr9:140762377-140762689	ENSG00000203987.2
4	lnc-AL772363.1-1	chr9:140762365-140762689	XLOC_007904

miRNA name	Chromosome Location	mirBase accession
hsa-miR-602	chr9:140732886-140732908	MIMAT0003270

No.	miRNA target gene	miRNA name	Chromosome Location
1	EHMT1	hsa-miR-615-3p	chr9:140729903-140729924
2	EHMT1	hsa-miR-30e-5p	chr9:140730456-140730473
3	EHMT1	hsa-miR-1	chr9:140730432-140730455

Variant related genes	Relation type
MIR602	TF binding region
EHMT1	TF binding region
MIR602	CpG island
EHMT1	CpG island
ENSG00000181090	chromatin interactions
ENSG00000207693	chromatin interactions
ACIN1	miRNA target sites

Extended variants
information (count: 3945 )
Associated
traits (count: 20 )

Variant overlapped rSNPs/rCNVs (count:3945 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs186183365	chr9:140689258-140689259	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs148373243	chr9:140689266-140689267	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs191033313	chr9:140689293-140689294	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs140573815	chr9:140689299-140689300	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs534297180	chr9:140689306-140689307	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs147088194	chr9:140689335-140689336	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs182766056	chr9:140689370-140689371	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs138396563	chr9:140689371-140689372	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs143892650	chr9:140689372-140689373	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs7023287	chr9:140689373-140689374	Strong transcription Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs373224769	chr9:140689401-140689402	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs80323354	chr9:140689402-140689403	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs186762609	chr9:140689403-140689404	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs147249892	chr9:140689482-140689483	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs545031776	chr9:140689525-140689526	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs565610715	chr9:140689543-140689544	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs531108519	chr9:140689570-140689571	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs11137230	chr9:140689582-140689583	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs370792436	chr9:140689583-140689584	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs544432621	chr9:140689589-140689590	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs561130995	chr9:140689639-140689640	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs192633004	chr9:140689716-140689717	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs548693656	chr9:140689775-140689776	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs565595127	chr9:140689795-140689796	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs554055210	chr9:140689853-140689854	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs35767210	chr9:140689854-140689855	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs528100509	chr9:140689871-140689872	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs200728025	chr9:140689874-140689875	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs199932751	chr9:140689875-140689876	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs372510717	chr9:140689876-140689877	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs56398445	chr9:140689879-140689880	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs57203379	chr9:140689880-140689881	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs57072562	chr9:140689881-140689882	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs199704951	chr9:140689882-140689883	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs57020709	chr9:140689883-140689884	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs201270552	chr9:140689884-140689885	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs58140446	chr9:140689885-140689886	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs61017523	chr9:140689887-140689888	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs11137231	chr9:140689889-140689890	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs114875725	chr9:140689894-140689895	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs58902957	chr9:140689899-140689900	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs55876895	chr9:140689904-140689905	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs58311718	chr9:140689911-140689912	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs58881007	chr9:140689918-140689919	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs562519687	chr9:140689937-140689938	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs117705928	chr9:140689944-140689945	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs571543851	chr9:140690008-140690009	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs139008405	chr9:140690025-140690026	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs12684765	chr9:140690034-140690035	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs567488406	chr9:140690050-140690051	Strong transcription Weak transcription Genic enhancers Enhancers	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:1659 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:140649800-140712400	Weak transcription	Psoas Muscle	Psoas
2	chr9:140650200-140700000	Strong transcription	Primary T cells from cord blood	blood
3	chr9:140664200-140698600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
4	chr9:140664200-140701000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr9:140664600-140708000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr9:140664800-140700000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr9:140665000-140700000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr9:140665200-140702000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr9:140665400-140697800	Strong transcription	Thymus	Thymus
10	chr9:140665400-140700800	Strong transcription	Fetal Stomach	stomach
11	chr9:140667200-140698000	Strong transcription	Dnd41	blood
12	chr9:140667200-140699000	Strong transcription	Primary neutrophils fromperipheralblood	blood
13	chr9:140668200-140698000	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
14	chr9:140668200-140699000	Strong transcription	Esophagus	oesophagus
15	chr9:140668200-140700000	Strong transcription	Fetal Brain Female	brain
16	chr9:140675000-140689800	Weak transcription	Fetal Brain Male	brain
17	chr9:140675600-140690800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr9:140675600-140698600	Strong transcription	Placenta	Placenta
19	chr9:140675800-140695600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
20	chr9:140676000-140690800	Strong transcription	Primary T helper cells PMA-I stimulated	--
21	chr9:140676400-140699400	Weak transcription	Fetal Heart	heart
22	chr9:140677400-140689400	Weak transcription	Pancreatic Islets	Pancreatic Islet
23	chr9:140678400-140689600	Weak transcription	Small Intestine	intestine
24	chr9:140679600-140700000	Strong transcription	Fetal Muscle Leg	muscle
25	chr9:140679600-140710200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
26	chr9:140680600-140700000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr9:140681000-140711400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr9:140681200-140700000	Strong transcription	HUES6 Cell Line	embryonic stem cell
29	chr9:140681200-140704400	Strong transcription	Fetal Muscle Trunk	muscle
30	chr9:140681200-140704600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr9:140681400-140698400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr9:140681400-140699200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
33	chr9:140681400-140699800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr9:140681400-140699800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr9:140681600-140700200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr9:140682400-140699200	Strong transcription	Primary T helper cells fromperipheralblood	blood
37	chr9:140683000-140696600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr9:140683000-140700200	Strong transcription	Monocytes-CD14+_RO01746	blood
39	chr9:140683600-140698200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
40	chr9:140683600-140698400	Strong transcription	Primary T cells fromperipheralblood	blood
41	chr9:140683600-140704200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr9:140683800-140698800	Strong transcription	Primary monocytes fromperipheralblood	blood
43	chr9:140683800-140700000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
44	chr9:140684200-140689800	Weak transcription	Stomach Mucosa	stomach
45	chr9:140684200-140699800	Strong transcription	Fetal Intestine Small	intestine
46	chr9:140684200-140703200	Strong transcription	Primary B cells from peripheral blood	blood
47	chr9:140684400-140691000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
48	chr9:140684600-140695200	Strong transcription	Muscle Satellite Cultured Cells	--
49	chr9:140684600-140698600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr9:140684600-140699800	Strong transcription	HUES64 Cell Line	embryonic stem cell

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