Variant report

Variant	rs1508148
Chromosome Location	chr11:106158277-106158278
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10750750	0.87[ASN][1000 genomes]
rs10791801	0.80[ASN][1000 genomes]
rs10895935	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10895938	0.83[ASN][1000 genomes]
rs11226982	0.82[ASN][1000 genomes]
rs11226987	0.90[ASN][1000 genomes]
rs12273190	0.91[EUR][1000 genomes]
rs12283696	0.82[EUR][1000 genomes]
rs12290323	0.91[EUR][1000 genomes]
rs12291279	0.82[EUR][1000 genomes]
rs12421469	0.91[EUR][1000 genomes]
rs12421840	0.91[EUR][1000 genomes]
rs1262373	0.93[EUR][1000 genomes]
rs1605565	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1828126	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1893856	0.91[EUR][1000 genomes]
rs1944770	0.91[EUR][1000 genomes]
rs2409624	0.87[ASN][1000 genomes]
rs4614415	0.82[EUR][1000 genomes]
rs4755146	0.87[ASN][1000 genomes]
rs483873	0.91[EUR][1000 genomes]
rs485681	0.91[EUR][1000 genomes]
rs488212	0.99[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs531851	0.93[EUR][1000 genomes]
rs542358	0.99[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs565672	0.91[EUR][1000 genomes]
rs594050	0.91[EUR][1000 genomes]
rs602407	0.93[EUR][1000 genomes]
rs617143	0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs633534	0.93[EUR][1000 genomes]
rs657786	0.93[EUR][1000 genomes]
rs660647	0.99[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs667501	0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7126969	0.80[ASN][1000 genomes]
rs7127780	0.91[EUR][1000 genomes]
rs7131594	0.89[EUR][1000 genomes]
rs726349	0.91[EUR][1000 genomes]
rs72985182	0.82[EUR][1000 genomes]
rs72987177	0.91[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1048381	chr11:105945117-106561574	Weak transcription Enhancers Active TSS Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
2	nsv898358	chr11:105999580-106182251	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv430428	chr11:106005901-106173046	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	esv2754854	chr11:106092790-106245790	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:106152800-106158800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr11:106157400-106158600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr11:106157600-106159800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr11:106157800-106159400	Weak transcription	NHDF-Ad	bronchial
5	chr11:106158000-106159600	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr11:106158200-106159600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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