Variant report

Variant	rs8005725
Chromosome Location	chr14:70638461-70638462
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10782459	0.95[AMR][1000 genomes];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11158836	0.95[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11158841	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12433044	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12434709	0.93[AMR][1000 genomes];0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12437377	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1425614	0.95[AMR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2893	0.94[AMR][1000 genomes];0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs34713959	0.95[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs55695995	0.94[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs56659354	0.94[AMR][1000 genomes];0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs59299321	0.89[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs61559466	0.95[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs72729901	0.93[AMR][1000 genomes];0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs72731804	0.93[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs72731811	0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs913479	0.89[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	nsv832826	chr14:70559589-70723464	Bivalent/Poised TSS Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv902075	chr14:70612618-70919016	Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:70634000-70642800	Weak transcription	Fetal Brain Male	brain
2	chr14:70637600-70638800	Enhancers	Skeletal Muscle Female	skeletal muscle
3	chr14:70637600-70639600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr14:70637600-70641200	Enhancers	Skeletal Muscle Male	skeletal muscle
5	chr14:70637800-70639400	Enhancers	Primary hematopoietic stem cells	blood
6	chr14:70637800-70639400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr14:70638000-70640000	Weak transcription	Psoas Muscle	Psoas
8	chr14:70638200-70639400	Enhancers	Primary hematopoietic stem cells short term culture	blood
9	chr14:70638400-70638800	Enhancers	Primary B cells from peripheral blood	blood
10	chr14:70638400-70639000	Enhancers	Monocytes-CD14+_RO01746	blood

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

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