Variant report

Variant	rs60162378
Chromosome Location	chr1:221166801-221166802
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs17009202	0.92[EUR][1000 genomes]
rs17009291	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4587571	1.00[EUR][1000 genomes]
rs57878357	0.92[EUR][1000 genomes]
rs58324444	0.92[EUR][1000 genomes]
rs58487387	1.00[EUR][1000 genomes]
rs60523812	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs60688199	0.92[EUR][1000 genomes]
rs60884344	0.92[EUR][1000 genomes]
rs6693203	0.92[EUR][1000 genomes]
rs73097451	0.92[EUR][1000 genomes]
rs73097458	0.85[AMR][1000 genomes]
rs73097461	0.92[EUR][1000 genomes]
rs73097472	0.92[EUR][1000 genomes]
rs73097476	0.92[EUR][1000 genomes]
rs73097478	0.92[EUR][1000 genomes]
rs73097479	0.92[EUR][1000 genomes]
rs7515981	0.83[AMR][1000 genomes];1.00[EUR][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	nsv997685	chr1:220993527-221863416	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
2	nsv535299	chr1:220993527-221863416	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
3	nsv873199	chr1:221136672-221451217	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:221166200-221173400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr1:221166400-221167400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr1:221166600-221167400	Enhancers	Primary neutrophils fromperipheralblood	blood
4	chr1:221166600-221168200	Enhancers	Primary B cells from cord blood	blood
5	chr1:221166600-221174600	Weak transcription	Psoas Muscle	Psoas

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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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