Variant report

Variant	rs74018300
Chromosome Location	chr16:48200213-48200214
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 61 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10163354	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10163462	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11861031	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11861127	0.84[ASN][1000 genomes]
rs11863133	0.93[ASN][1000 genomes]
rs11863233	0.93[ASN][1000 genomes]
rs11863236	0.93[ASN][1000 genomes]
rs11863325	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11866251	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11866312	0.93[ASN][1000 genomes]
rs11866529	0.93[ASN][1000 genomes]
rs13336264	0.86[ASN][1000 genomes]
rs16945916	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16945917	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16945919	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16945972	0.93[ASN][1000 genomes]
rs16945974	0.85[ASN][1000 genomes]
rs17743256	1.00[ASN][1000 genomes]
rs28376623	0.93[ASN][1000 genomes]
rs28503414	0.93[ASN][1000 genomes]
rs28605399	0.85[ASN][1000 genomes]
rs28626252	0.93[ASN][1000 genomes]
rs28654935	0.93[ASN][1000 genomes]
rs28684834	0.93[ASN][1000 genomes]
rs28696036	0.93[ASN][1000 genomes]
rs41280939	1.00[ASN][1000 genomes]
rs5017203	0.93[ASN][1000 genomes]
rs57912486	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62058521	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62058522	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62058526	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62058528	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6500339	0.92[ASN][1000 genomes]
rs7184831	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7187233	1.00[ASN][1000 genomes]
rs7191844	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7203695	1.00[ASN][1000 genomes]
rs7206909	1.00[ASN][1000 genomes]
rs73540901	0.93[ASN][1000 genomes]
rs73542903	0.93[ASN][1000 genomes]
rs73542904	0.93[ASN][1000 genomes]
rs73546434	0.85[ASN][1000 genomes]
rs73546437	0.85[ASN][1000 genomes]
rs73546439	0.85[ASN][1000 genomes]
rs74018298	0.92[ASN][1000 genomes]
rs8046814	0.93[ASN][1000 genomes]
rs8047091	0.93[ASN][1000 genomes]
rs8047397	0.85[ASN][1000 genomes]
rs8050120	1.00[ASN][1000 genomes]
rs8051016	0.93[ASN][1000 genomes]
rs8051205	0.93[ASN][1000 genomes]
rs8055128	0.85[ASN][1000 genomes]
rs8056100	0.85[ASN][1000 genomes]
rs8056143	0.85[ASN][1000 genomes]
rs8057475	0.93[ASN][1000 genomes]
rs8060696	0.85[ASN][1000 genomes]
rs8060722	0.85[ASN][1000 genomes]
rs957881	1.00[ASN][1000 genomes]
rs9932850	0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1059259	chr16:48113396-48304404	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv542916	chr16:48113396-48304404	Strong transcription Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:48192800-48204000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr16:48198800-48200400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr16:48198800-48204800	Enhancers	Primary neutrophils fromperipheralblood	blood
4	chr16:48199000-48200600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr16:48199000-48201200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
6	chr16:48199200-48226600	Weak transcription	Spleen	Spleen
7	chr16:48199600-48200400	Flanking Active TSS	HepG2	liver
8	chr16:48199600-48202000	Weak transcription	Adipose Nuclei	Adipose
9	chr16:48200200-48200400	Enhancers	Primary monocytes fromperipheralblood	blood
10	chr16:48200200-48201200	Weak transcription	Monocytes-CD14+_RO01746	blood
11	chr16:48200200-48209000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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