Variant report

Variant	rs7074313
Chromosome Location	chr10:118224919-118224920
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs10749215	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10749218	0.80[AMR][1000 genomes]
rs10787675	0.93[ASN][1000 genomes]
rs10885966	0.83[AMR][1000 genomes]
rs11197685	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11197692	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1431481	0.93[ASN][1000 genomes]
rs1897515	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1897516	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4751970	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7069270	0.99[ASN][1000 genomes]
rs891665	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832001	chr10:118138370-118315059	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 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	chr10:118202000-118225400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr10:118214200-118225200	Strong transcription	HMEC	breast
3	chr10:118222800-118226000	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr10:118224000-118226600	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr10:118224200-118226800	Genic enhancers	NHEK	skin
6	chr10:118224400-118226000	Enhancers	Primary hematopoietic stem cells short term culture	blood
7	chr10:118224400-118226600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr10:118224400-118226600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr10:118224400-118231200	Weak transcription	Pancreas	Pancrea
10	chr10:118224600-118225200	Enhancers	Monocytes-CD14+_RO01746	blood
11	chr10:118224800-118226200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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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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