Variant report

Variant	rs11100963
Chromosome Location	chr4:148375799-148375800
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 75 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:74)

rs_ID	r²[population]
rs10011966	0.80[CHB][hapmap];0.86[JPT][hapmap];1.00[YRI][hapmap]
rs10024834	0.81[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap]
rs10305860	0.85[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs10305862	0.88[ASN][1000 genomes]
rs11722878	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11722942	0.99[ASN][1000 genomes]
rs11727337	0.99[ASN][1000 genomes]
rs11727397	0.99[ASN][1000 genomes]
rs11730985	0.99[ASN][1000 genomes]
rs11731096	0.95[ASN][1000 genomes]
rs11731097	0.95[ASN][1000 genomes]
rs11731134	0.99[ASN][1000 genomes]
rs12509416	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12642328	0.99[ASN][1000 genomes]
rs13109203	0.80[AFR][1000 genomes];0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13109209	0.85[AFR][1000 genomes];0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13112065	0.99[ASN][1000 genomes]
rs13127894	0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13138887	0.93[ASN][1000 genomes]
rs13144507	0.97[ASN][1000 genomes]
rs1366688	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1400558	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs1400559	0.99[ASN][1000 genomes]
rs1400560	0.99[ASN][1000 genomes]
rs1517134	0.83[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs1517138	0.99[ASN][1000 genomes]
rs1517139	0.99[ASN][1000 genomes]
rs17474816	0.81[CHB][hapmap];0.90[JPT][hapmap]
rs1801708	0.85[CHB][hapmap];0.95[JPT][hapmap];0.90[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs1808038	0.84[ASN][1000 genomes]
rs1808039	0.87[AFR][1000 genomes];0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1949375	0.99[ASN][1000 genomes]
rs1987147	0.86[EUR][1000 genomes]
rs1996373	0.90[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs1996374	0.85[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs2063936	0.99[ASN][1000 genomes]
rs34256803	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35686091	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36129328	0.89[ASN][1000 genomes]
rs4631019	0.97[ASN][1000 genomes]
rs4835081	0.99[ASN][1000 genomes]
rs4835083	0.90[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs4835084	0.86[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs4835401	0.99[ASN][1000 genomes]
rs4835405	0.99[ASN][1000 genomes]
rs4835407	0.99[ASN][1000 genomes]
rs4835410	0.88[ASN][1000 genomes]
rs56015601	0.88[ASN][1000 genomes]
rs6537479	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs6537480	0.90[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs6537483	0.81[CHB][hapmap];0.90[JPT][hapmap];1.00[YRI][hapmap]
rs6537484	0.86[JPT][hapmap]
rs6810637	0.86[ASN][1000 genomes]
rs6817469	0.97[ASN][1000 genomes]
rs6819740	0.81[CHB][hapmap];0.86[JPT][hapmap]
rs6820938	0.87[ASN][1000 genomes]
rs6823537	1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs6835512	0.92[ASN][1000 genomes]
rs6840108	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6840756	0.81[CHB][hapmap];0.90[JPT][hapmap]
rs6840784	0.90[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6848108	0.81[CHB][hapmap];0.90[JPT][hapmap]
rs6853791	0.86[ASN][1000 genomes]
rs6855875	0.85[CHB][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs702757	0.81[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs7655670	0.81[CHB][hapmap];0.86[JPT][hapmap]
rs7659823	0.88[ASN][1000 genomes]
rs7663891	0.84[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs9308218	0.90[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs952402	0.86[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs959600	0.99[ASN][1000 genomes]
rs984457	0.85[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs984458	0.81[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs9991584	0.90[AFR][1000 genomes];0.80[AMR][1000 genomes];0.88[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	nsv830109	chr4:148295061-148468605	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:148375200-148377600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr4:148375200-148378000	Weak transcription	HMEC	breast
3	chr4:148375600-148376600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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