Variant report

Variant	rs16926114
Chromosome Location	chr8:61304790-61304791
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:61300352..61302588-chr8:61303599..61306089,2	K562	blood:
2	chr8:61304106..61306671-chr8:61306892..61309869,2	K562	blood:

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs16918848	1.00[AMR][1000 genomes]
rs16926079	1.00[AMR][1000 genomes]
rs16926106	1.00[ASN][1000 genomes]
rs16926108	1.00[ASN][1000 genomes]
rs16926113	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs16926128	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs16926130	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs16926275	1.00[AMR][1000 genomes]
rs59690563	1.00[AMR][1000 genomes]
rs60618306	1.00[AMR][1000 genomes]
rs6991970	1.00[ASN][1000 genomes]
rs73243948	1.00[AMR][1000 genomes]
rs73243989	1.00[AMR][1000 genomes]
rs73243992	1.00[AMR][1000 genomes]
rs73243994	1.00[AMR][1000 genomes]
rs73245610	1.00[AMR][1000 genomes]
rs73245619	1.00[AMR][1000 genomes]
rs73245642	1.00[AMR][1000 genomes]
rs73247786	1.00[AMR][1000 genomes]
rs73250102	1.00[ASN][1000 genomes]
rs73251503	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv917756	chr8:60942299-61862796	Enhancers Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
2	nsv1022752	chr8:61095248-61322302	Weak transcription Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
3	esv3371465	chr8:61115030-61356658	Bivalent Enhancer Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
4	nsv831334	chr8:61148796-61330190	Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
5	nsv890944	chr8:61252500-61307115	Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent/Poised TSS 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	chr8:61302400-61308800	Weak transcription	Brain Hippocampus Middle	brain
2	chr8:61304200-61305000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr8:61304400-61304800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr8:61304400-61306200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr8:61304600-61305600	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr8:61304600-61306400	Enhancers	Monocytes-CD14+_RO01746	blood

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