Variant report

Variant	rs60582277
Chromosome Location	chr1:69978799-69978800
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs17130981	1.00[EUR][1000 genomes]
rs72934427	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72934445	1.00[EUR][1000 genomes]
rs72934446	1.00[EUR][1000 genomes]
rs72934447	1.00[EUR][1000 genomes]
rs72934448	1.00[EUR][1000 genomes]
rs72934450	1.00[EUR][1000 genomes]
rs72934460	1.00[EUR][1000 genomes]
rs7516848	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7531804	1.00[EUR][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	nsv949691	chr1:69749722-70302201	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	esv3384194	chr1:69885024-70275430	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:69972800-69986200	Weak transcription	K562	blood
2	chr1:69976800-69979000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr1:69976800-69979200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr1:69977000-69978800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr1:69977000-69978800	Weak transcription	HMEC	breast
6	chr1:69977000-69979400	Weak transcription	NHDF-Ad	bronchial
7	chr1:69978600-69980000	Enhancers	NHEK	skin

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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

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