Variant report

Variant	rs3005191
Chromosome Location	chr10:25776176-25776177
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:25775286..25778319-chr10:25779933..25782131,3	K562	blood:
2	chr10:25766789..25768735-chr10:25775251..25777861,2	K562	blood:

Extended variants
information (count: 64 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:63)

rs_ID	r²[population]
rs10508695	1.00[CHB][hapmap];0.96[CHD][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs10508696	1.00[CHB][hapmap];0.96[CHD][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs1069531	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11014576	0.99[ASN][1000 genomes]
rs12415532	0.89[CHB][hapmap];0.88[CHD][hapmap];0.92[JPT][hapmap];0.90[ASN][1000 genomes]
rs12763436	1.00[CHB][hapmap];0.92[CHD][hapmap];0.95[ASN][1000 genomes]
rs12766947	0.99[ASN][1000 genomes]
rs12770449	0.95[ASN][1000 genomes]
rs12770880	0.95[ASN][1000 genomes]
rs12778509	0.99[ASN][1000 genomes]
rs1329255	0.85[CEU][hapmap];0.92[JPT][hapmap];0.83[ASN][1000 genomes]
rs1329256	0.84[CEU][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs1329257	0.91[JPT][hapmap];0.84[ASN][1000 genomes]
rs1360123	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1361634	0.92[CEU][hapmap];1.00[CHB][hapmap];0.92[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.81[TSI][hapmap];0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1410931	0.96[CEU][hapmap];1.00[CHB][hapmap];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1590833	0.89[CHB][hapmap];0.92[JPT][hapmap];0.86[ASN][1000 genomes]
rs1592137	0.88[CHB][hapmap];0.91[JPT][hapmap];0.89[ASN][1000 genomes]
rs1620326	0.89[CEU][hapmap];1.00[CHB][hapmap];0.96[CHD][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs1773636	0.91[CEU][hapmap];0.94[EUR][1000 genomes]
rs1773637	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1928365	0.85[CEU][hapmap];0.84[JPT][hapmap];0.83[ASN][1000 genomes]
rs2211344	0.88[EUR][1000 genomes]
rs2480348	0.96[CEU][hapmap];1.00[CHB][hapmap];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2480349	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2487819	1.00[CEU][hapmap];1.00[CHB][hapmap];0.85[GIH][hapmap];0.88[MEX][hapmap];0.84[TSI][hapmap];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2987832	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2987833	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2987834	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2987835	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2987836	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2987838	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.92[MEX][hapmap];0.93[TSI][hapmap];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2987839	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2987840	0.83[ASN][1000 genomes]
rs3005181	0.83[ASN][1000 genomes]
rs3005182	0.85[CEU][hapmap];0.92[JPT][hapmap];0.83[MEX][hapmap];0.83[ASN][1000 genomes]
rs3005187	0.81[ASN][1000 genomes]
rs3005189	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3005193	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3005194	0.94[EUR][1000 genomes]
rs3123901	0.83[ASN][1000 genomes]
rs34535236	0.99[ASN][1000 genomes]
rs36146927	0.94[ASN][1000 genomes]
rs4408231	0.93[EUR][1000 genomes]
rs4545439	0.89[CHB][hapmap];0.88[CHD][hapmap];0.86[ASN][1000 genomes]
rs4630196	0.85[EUR][1000 genomes]
rs57048226	0.99[ASN][1000 genomes]
rs66516873	0.99[ASN][1000 genomes]
rs67290477	0.99[ASN][1000 genomes]
rs67616835	0.99[ASN][1000 genomes]
rs702977	0.89[EUR][1000 genomes]
rs702980	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.87[GIH][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap];0.91[TSI][hapmap];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7075106	0.92[ASN][1000 genomes]
rs7084979	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs7085111	0.99[ASN][1000 genomes]
rs7086959	0.92[ASN][1000 genomes]
rs7089568	0.96[ASN][1000 genomes]
rs824588	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs824589	0.96[CEU][hapmap];0.81[GIH][hapmap];0.83[TSI][hapmap];0.87[EUR][1000 genomes]
rs824607	0.96[CEU][hapmap];1.00[CHB][hapmap];0.92[CHD][hapmap];0.87[GIH][hapmap];1.00[JPT][hapmap];0.87[TSI][hapmap];0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs824608	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs824609	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs824610	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.87[GIH][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap];0.93[TSI][hapmap];0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3349863	chr10:25614571-25946379	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs3005191	BAMBI	cis	cerebellum	SCAN

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:25765800-25782800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr10:25769600-25777800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr10:25775400-25777000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr10:25775600-25777000	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr10:25775600-25782400	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr10:25775800-25781200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr10:25776000-25777200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
8	chr10:25776000-25777200	Enhancers	K562	blood

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