Variant report

Variant	rs714784
Chromosome Location	chr15:51296407-51296408
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:51294396..51297961-chr15:51303486..51306032,4	MCF-7	breast:
2	chr15:51295995..51298395-chr15:51304448..51306643,2	K562	blood:
3	chr15:51291205..51293586-chr15:51295026..51296629,2	MCF-7	breast:
4	chr15:51295054..51296990-chr15:51420438..51423061,2	K562	blood:
5	chr15:51291454..51293095-chr15:51294731..51296517,2	K562	blood:

Extended variants
information (count: 140 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:129)

rs_ID	r²[population]
rs10744956	0.91[CHB][hapmap];0.85[CHD][hapmap];0.82[JPT][hapmap];0.83[ASN][1000 genomes]
rs10851494	0.81[CHB][hapmap];0.81[JPT][hapmap]
rs11070824	0.91[CHB][hapmap];0.95[JPT][hapmap];0.82[ASN][1000 genomes]
rs11070829	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11070835	0.90[CHB][hapmap]
rs1147128	0.88[ASN][1000 genomes]
rs1147129	0.86[CHB][hapmap];0.91[CHD][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs1147130	0.88[ASN][1000 genomes]
rs1147131	0.86[CHB][hapmap];0.95[JPT][hapmap];0.87[ASN][1000 genomes]
rs1147133	0.88[ASN][1000 genomes]
rs1147135	0.88[ASN][1000 genomes]
rs1147136	0.88[ASN][1000 genomes]
rs1147139	0.87[ASN][1000 genomes]
rs11632971	0.91[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11635015	0.96[CEU][hapmap];0.95[CHB][hapmap];0.91[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11635102	0.96[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11857810	0.81[CHB][hapmap]
rs12438343	0.86[CHB][hapmap];0.95[JPT][hapmap];0.89[ASN][1000 genomes]
rs12440387	0.81[CHB][hapmap]
rs12441714	0.93[AFR][1000 genomes];0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12595034	0.89[ASN][1000 genomes]
rs12708425	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1276854	0.86[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.84[ASN][1000 genomes]
rs12898208	0.89[ASN][1000 genomes]
rs12898530	0.89[ASN][1000 genomes]
rs12904125	0.87[ASN][1000 genomes]
rs12904382	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12905611	0.87[ASN][1000 genomes]
rs12906866	0.90[CHB][hapmap];0.95[JPT][hapmap];0.85[YRI][hapmap];0.93[ASN][1000 genomes]
rs12908516	0.82[ASN][1000 genomes]
rs12909519	0.96[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12912295	0.84[AFR][1000 genomes];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12916407	0.87[ASN][1000 genomes]
rs1371058	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1472946	0.90[CHB][hapmap];0.82[JPT][hapmap];0.82[ASN][1000 genomes]
rs1509423	0.95[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1550336	1.00[ASW][hapmap];1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.96[MEX][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1550340	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17703090	0.91[CHB][hapmap];0.82[JPT][hapmap];0.82[ASN][1000 genomes]
rs2118785	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2127366	0.88[ASN][1000 genomes]
rs2127367	0.89[ASN][1000 genomes]
rs2127368	0.86[CHB][hapmap];0.95[JPT][hapmap];0.89[ASN][1000 genomes]
rs2170011	0.89[ASN][1000 genomes]
rs2249535	0.86[CHB][hapmap];0.91[CHD][hapmap];0.95[JPT][hapmap];0.86[YRI][hapmap];0.88[ASN][1000 genomes]
rs2306331	0.86[CHB][hapmap];0.91[CHD][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs2306332	0.92[AFR][1000 genomes];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2414078	0.88[ASN][1000 genomes]
rs2414079	0.88[ASN][1000 genomes]
rs2414080	0.84[ASN][1000 genomes]
rs2414081	0.86[CHB][hapmap];0.95[JPT][hapmap];0.89[ASN][1000 genomes]
rs2614776	0.86[CHB][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs2614779	0.86[CHB][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs2614780	0.86[CHB][hapmap];0.91[CHD][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs2614781	0.86[CHB][hapmap];0.95[JPT][hapmap];0.86[YRI][hapmap];0.88[ASN][1000 genomes]
rs2614782	0.88[ASN][1000 genomes]
rs2614784	0.88[ASN][1000 genomes]
rs2614789	0.88[ASN][1000 genomes]
rs2614790	0.86[CHB][hapmap];0.95[JPT][hapmap];0.84[YRI][hapmap];0.88[ASN][1000 genomes]
rs2614791	0.90[CHB][hapmap];0.82[JPT][hapmap];0.82[ASN][1000 genomes]
rs2614792	0.85[CHB][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs2614794	0.86[CHB][hapmap];0.95[JPT][hapmap];0.86[YRI][hapmap];0.88[ASN][1000 genomes]
rs2619686	0.86[CHB][hapmap];0.95[JPT][hapmap];0.86[YRI][hapmap];0.88[ASN][1000 genomes]
rs2619687	0.88[ASN][1000 genomes]
rs2619688	0.88[ASN][1000 genomes]
rs2619691	0.86[CHB][hapmap];0.82[CHD][hapmap];0.82[JPT][hapmap]
rs2619693	0.86[ASN][1000 genomes]
rs2619694	0.87[ASN][1000 genomes]
rs2663533	0.85[CHB][hapmap];0.93[CHD][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs2663535	0.86[CHB][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs2663537	0.87[ASN][1000 genomes]
rs2663538	0.86[CHB][hapmap];0.95[JPT][hapmap];0.87[ASN][1000 genomes]
rs2663541	0.88[ASN][1000 genomes]
rs2663543	0.88[ASN][1000 genomes]
rs2663544	0.88[ASN][1000 genomes]
rs2663545	0.88[ASN][1000 genomes]
rs2663546	0.88[ASN][1000 genomes]
rs2663548	0.86[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs2663553	0.86[CHB][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs2663554	0.84[CHB][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs2663555	0.88[ASN][1000 genomes]
rs2663556	0.86[CHB][hapmap];0.95[JPT][hapmap];0.86[YRI][hapmap];0.81[ASN][1000 genomes]
rs3743045	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3784301	0.84[CHD][hapmap];0.86[JPT][hapmap];0.83[ASN][1000 genomes]
rs3784302	0.87[CEU][hapmap];0.86[CHB][hapmap];0.86[CHD][hapmap];0.81[GIH][hapmap];0.86[JPT][hapmap];0.87[MEX][hapmap];0.87[ASN][1000 genomes]
rs3784303	0.86[CHB][hapmap];0.95[JPT][hapmap];0.87[ASN][1000 genomes]
rs4438254	0.89[ASN][1000 genomes]
rs4444282	0.92[AFR][1000 genomes];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4534781	0.89[ASN][1000 genomes]
rs4775910	0.91[CHB][hapmap];0.82[JPT][hapmap];0.82[ASN][1000 genomes]
rs4775913	0.87[ASN][1000 genomes]
rs56115630	0.85[ASN][1000 genomes]
rs6493469	0.86[CHB][hapmap];0.91[CHD][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs6493471	0.85[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6493472	0.90[ASN][1000 genomes]
rs6493473	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6493476	1.00[ASW][hapmap];1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.96[MEX][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs67145268	0.83[ASN][1000 genomes]
rs67228714	0.85[ASN][1000 genomes]
rs7162209	1.00[ASW][hapmap];0.96[CEU][hapmap];0.95[CHB][hapmap];0.98[CHD][hapmap];0.95[GIH][hapmap];0.95[JPT][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];0.93[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7168385	0.86[CHB][hapmap];0.95[JPT][hapmap];0.89[ASN][1000 genomes]
rs7168846	0.86[CHB][hapmap];0.95[JPT][hapmap];0.89[ASN][1000 genomes]
rs7169888	0.89[ASN][1000 genomes]
rs7170311	0.85[AFR][1000 genomes];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7170365	0.89[ASN][1000 genomes]
rs7170675	0.86[CHB][hapmap];0.91[CHD][hapmap];0.95[JPT][hapmap];0.89[ASN][1000 genomes]
rs7171085	0.89[ASN][1000 genomes]
rs7177267	0.89[ASN][1000 genomes]
rs7180258	0.91[CHB][hapmap];0.95[JPT][hapmap];0.92[ASN][1000 genomes]
rs7181051	0.89[ASN][1000 genomes]
rs7181201	0.91[CHB][hapmap];0.93[CHD][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs7181997	0.88[ASN][1000 genomes]
rs7182957	0.86[CHB][hapmap];0.95[JPT][hapmap];0.93[ASN][1000 genomes]
rs7184026	0.88[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs73408568	0.80[ASN][1000 genomes]
rs7494977	0.87[ASN][1000 genomes]
rs8024428	0.89[ASN][1000 genomes]
rs8025456	0.85[ASN][1000 genomes]
rs8026318	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8029155	0.86[CHB][hapmap];0.91[CHD][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs8029369	0.86[CHB][hapmap];0.95[JPT][hapmap];0.89[ASN][1000 genomes]
rs8030124	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8030214	0.96[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];1.00[MEX][hapmap];0.93[MKK][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs8031702	0.86[CHB][hapmap];0.91[CHD][hapmap];0.95[JPT][hapmap];0.86[YRI][hapmap];0.88[ASN][1000 genomes]
rs8033934	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs8034236	0.81[ASN][1000 genomes]
rs8034576	0.83[ASN][1000 genomes]
rs8035358	0.95[CEU][hapmap];0.95[CHB][hapmap];0.94[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs8041824	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1047443	chr15:50744781-51647023	Strong transcription Active TSS Weak transcription Genic enhancers Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
2	nsv569399	chr15:50874964-51562198	Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
3	nsv569400	chr15:50874964-51767265	ZNF genes & repeats Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
4	nsv428636	chr15:51154834-51298044	Active TSS Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
5	nsv569403	chr15:51191421-51304373	Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
6	nsv1038778	chr15:51196641-51356728	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
7	nsv904214	chr15:51204364-51535192	Strong transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
8	nsv1049644	chr15:51265447-51560445	Strong transcription Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
9	esv34532	chr15:51276128-51752856	Flanking Active TSS Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
10	esv2758382	chr15:51282257-51830339	Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
11	esv2760031	chr15:51282257-51830339	Weak transcription Enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs714784	GABPB1	cis	parietal	SCAN

Chromatin state (count:118 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:51210600-51298400	Weak transcription	Stomach Mucosa	stomach
2	chr15:51261600-51298200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
3	chr15:51263000-51304800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr15:51263600-51297800	Weak transcription	NHLF	lung
5	chr15:51263600-51299200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr15:51263600-51300200	Weak transcription	Small Intestine	intestine
7	chr15:51263600-51301200	Weak transcription	HepG2	liver
8	chr15:51263600-51303000	Weak transcription	HUVEC	blood vessel
9	chr15:51263800-51296600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
10	chr15:51263800-51300400	Weak transcription	Right Ventricle	heart
11	chr15:51264600-51296600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
12	chr15:51265200-51302400	Weak transcription	Brain Hippocampus Middle	brain
13	chr15:51265200-51315600	Weak transcription	Gastric	stomach
14	chr15:51265400-51302400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
15	chr15:51267000-51302200	Weak transcription	Fetal Brain Female	brain
16	chr15:51270200-51302600	Weak transcription	Skeletal Muscle Male	skeletal muscle
17	chr15:51270200-51317600	Weak transcription	Psoas Muscle	Psoas
18	chr15:51273400-51298000	Weak transcription	Lung	lung
19	chr15:51273400-51302200	Weak transcription	Colonic Mucosa	Colon
20	chr15:51273400-51302400	Weak transcription	Rectal Smooth Muscle	rectum
21	chr15:51273600-51296800	Weak transcription	Spleen	Spleen
22	chr15:51273600-51298200	Weak transcription	Brain Cingulate Gyrus	brain
23	chr15:51273600-51307600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr15:51274200-51301800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr15:51276400-51300600	Weak transcription	A549	lung
26	chr15:51282000-51304000	Weak transcription	Fetal Heart	heart
27	chr15:51282600-51301000	Weak transcription	Colon Smooth Muscle	Colon
28	chr15:51283400-51300400	Weak transcription	Fetal Intestine Small	intestine
29	chr15:51283600-51299600	Weak transcription	Brain Substantia Nigra	brain
30	chr15:51284600-51296600	Weak transcription	Pancreatic Islets	Pancreatic Islet
31	chr15:51286200-51315600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr15:51286600-51323000	Weak transcription	Brain Inferior Temporal Lobe	brain
33	chr15:51287400-51300600	Weak transcription	Rectal Mucosa Donor 31	rectum
34	chr15:51288400-51296600	Strong transcription	Primary T cells fromperipheralblood	blood
35	chr15:51288400-51297800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
36	chr15:51288600-51296800	Strong transcription	Placenta	Placenta
37	chr15:51289000-51302000	Weak transcription	Stomach Smooth Muscle	stomach
38	chr15:51289000-51322200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr15:51289400-51296800	Strong transcription	HSMM	muscle
40	chr15:51289400-51298800	Weak transcription	Muscle Satellite Cultured Cells	--
41	chr15:51290000-51300400	Weak transcription	Sigmoid Colon	Sigmoid Colon
42	chr15:51290800-51300400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
43	chr15:51291800-51298000	Weak transcription	Fetal Kidney	kidney
44	chr15:51292400-51296800	Strong transcription	Adipose Nuclei	Adipose
45	chr15:51292800-51296800	Strong transcription	Duodenum Mucosa	Duodenum
46	chr15:51293200-51296600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr15:51294200-51299200	Weak transcription	Primary T helper cells fromperipheralblood	blood
48	chr15:51294600-51296800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
49	chr15:51294600-51303200	Weak transcription	Primary hematopoietic stem cells	blood
50	chr15:51294800-51298200	Weak transcription	GM12878-XiMat	blood

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