Variant report

Variant	rs74043907
Chromosome Location	chr14:31746682-31746683
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10149460	0.80[AMR][1000 genomes]
rs10467704	0.80[AMR][1000 genomes]
rs12100784	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12100791	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12589391	0.80[AMR][1000 genomes]
rs28758850	0.80[AMR][1000 genomes]
rs55719863	0.91[AMR][1000 genomes]
rs61107917	0.80[AMR][1000 genomes]
rs61408696	0.80[AMR][1000 genomes]
rs61416910	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61741258	0.83[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs7142843	0.80[AMR][1000 genomes]
rs7158422	0.80[AMR][1000 genomes]
rs74043915	0.81[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs74043923	0.80[AMR][1000 genomes]
rs74043937	0.80[AMR][1000 genomes]
rs74043941	0.80[AMR][1000 genomes]
rs8003524	0.80[AMR][1000 genomes]
rs8003996	0.80[AMR][1000 genomes]
rs8007156	0.90[AMR][1000 genomes]
rs8012411	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8014570	0.80[AMR][1000 genomes]
rs8020685	0.91[AMR][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	nsv901587	chr14:31501505-31752664	Strong transcription Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	esv2830427	chr14:31639110-32000034	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
3	nsv1050597	chr14:31711248-31904761	Strong transcription Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:31743600-31753000	Weak transcription	Osteobl	bone
2	chr14:31744200-31746800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
3	chr14:31746000-31749600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr14:31746600-31755400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

what's new

Quick links