Variant report

Variant	rs74150670
Chromosome Location	chr10:93144029-93144030
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs11186558	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11186560	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11186565	0.82[ASN][1000 genomes]
rs12240706	0.84[ASN][1000 genomes]
rs12241174	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12242238	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12242821	0.84[ASN][1000 genomes]
rs12247672	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12253137	0.84[ASN][1000 genomes]
rs12268013	0.84[ASN][1000 genomes]
rs17106645	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4586060	0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs57033814	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs57996677	0.86[ASN][1000 genomes]
rs60640820	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6583769	0.91[ASN][1000 genomes]
rs6583770	0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7077715	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7081363	0.82[EUR][1000 genomes]
rs7091647	0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs73316210	0.86[ASN][1000 genomes]
rs73316216	0.84[ASN][1000 genomes]
rs7893331	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7893826	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7898769	0.84[ASN][1000 genomes]
rs7904917	0.84[ASN][1000 genomes]
rs7905307	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7906515	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7907154	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7910864	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7911332	0.91[ASN][1000 genomes]
rs7915331	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7916523	0.84[ASN][1000 genomes]
rs7920500	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:93140000-93145600	Enhancers	Fetal Brain Male	brain
2	chr10:93141800-93144800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr10:93142400-93144600	Weak transcription	Fetal Brain Female	brain
4	chr10:93142400-93149400	Weak transcription	Fetal Lung	lung
5	chr10:93142400-93149800	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr10:93142600-93149600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr10:93143200-93144400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr10:93143200-93147200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr10:93143400-93144200	Bivalent Enhancer	Primary mononuclear cells fromperipheralblood	Blood
10	chr10:93144000-93144200	Flanking Bivalent TSS/Enh	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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