Variant report

Variant	rs4105126
Chromosome Location	chr12:29353737-29353738
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 62 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs10743645	0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10743647	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10743648	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10743649	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10771486	0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10771489	0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10771492	0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10771494	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10843343	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11050084	0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11050098	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11050099	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11050104	0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11050108	0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11050110	0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11050112	0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11050114	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12310732	0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12366549	0.84[EUR][1000 genomes]
rs1496218	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1561132	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1826800	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1845819	0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1908690	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1908691	0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2349974	0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4105125	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4105127	0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4105128	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4141943	0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4141945	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4323913	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4536271	0.88[ASN][1000 genomes]
rs4930856	0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4930857	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4930858	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4930859	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4931158	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4931162	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4931163	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4931165	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60287933	0.88[ASN][1000 genomes]
rs6487778	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6487783	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs71453727	0.91[ASN][1000 genomes]
rs7294355	0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7296268	0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7297542	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs73265795	0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7956130	0.90[AMR][1000 genomes]
rs7956134	0.87[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs7968949	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7974769	0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7975191	0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7980923	0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs924105	0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs924107	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs924109	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs958478	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532233	chr12:29009388-29496179	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
2	nsv995123	chr12:29095272-29571558	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
3	nsv1053641	chr12:29268813-29854413	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:29325400-29364600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr12:29328800-29354200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr12:29336000-29354000	Weak transcription	Primary hematopoietic stem cells	blood
4	chr12:29346000-29360800	Weak transcription	Duodenum Mucosa	Duodenum
5	chr12:29352000-29355600	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr12:29353200-29354000	Enhancers	Rectal Mucosa Donor 31	rectum
7	chr12:29353200-29354200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr12:29353400-29353800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links