Variant report

Variant	rs726349
Chromosome Location	chr11:106080025-106080026
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10750750	0.84[CEU][hapmap]
rs10895935	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12273190	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12276977	0.84[AFR][1000 genomes];0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12283696	0.92[AFR][1000 genomes];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12290323	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12291279	0.89[AFR][1000 genomes];0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12294538	0.84[AFR][1000 genomes];0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12421469	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12421840	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1262373	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1396156	0.81[CHB][hapmap]
rs1508148	0.91[EUR][1000 genomes]
rs1605565	0.83[EUR][1000 genomes]
rs1605567	0.81[CHB][hapmap]
rs1806481	0.81[CHB][hapmap];0.81[CHD][hapmap]
rs1828126	0.91[EUR][1000 genomes]
rs1893856	0.97[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1940761	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1944770	0.97[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4614415	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4755146	0.84[CEU][hapmap]
rs483873	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs485681	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs488212	0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs505416	0.84[EUR][1000 genomes]
rs531851	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs542358	0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs565672	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs594050	0.84[EUR][1000 genomes]
rs602407	1.00[CEU][hapmap];0.95[CHB][hapmap];0.84[JPT][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs617143	0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs633534	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs657786	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs660647	0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs667501	0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs674799	0.85[CEU][hapmap];0.85[CHB][hapmap]
rs7120502	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7127780	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7131594	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72983168	0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72985182	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs72987177	0.96[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][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	nsv826073	chr11:106064382-106122340	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:106078400-106084600	Enhancers	Fetal Intestine Small	intestine
2	chr11:106078400-106084800	Enhancers	Fetal Intestine Large	intestine
3	chr11:106079000-106080200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr11:106079000-106080600	Enhancers	Duodenum Mucosa	Duodenum
5	chr11:106079200-106080400	Enhancers	Fetal Kidney	kidney
6	chr11:106079200-106080400	Enhancers	HepG2	liver
7	chr11:106079600-106080200	Enhancers	Gastric	stomach
8	chr11:106079800-106080400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr11:106079800-106080400	Enhancers	Small Intestine	intestine
10	chr11:106079800-106084200	Weak transcription	Pancreas	Pancrea

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