Variant report

Variant	rs974363
Chromosome Location	chr1:173071389-173071390
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10753070	0.92[EUR][1000 genomes]
rs10912533	0.98[EUR][1000 genomes]
rs11799493	0.87[EUR][1000 genomes]
rs12034497	0.92[EUR][1000 genomes]
rs12743990	0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2422272	0.89[EUR][1000 genomes]
rs2901697	0.89[EUR][1000 genomes]
rs4916297	0.88[EUR][1000 genomes]
rs4916304	0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4916306	0.94[EUR][1000 genomes]
rs6413826	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6425203	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6425205	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6674831	0.98[EUR][1000 genomes]
rs9286880	0.86[CEU][hapmap]
rs9425406	0.83[EUR][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	nsv533953	chr1:172939335-173133255	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:173066400-173071800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr1:173066400-173072400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr1:173070600-173072000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	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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