Variant report

Variant	rs13140736
Chromosome Location	chr4:148309369-148309370
allele	A/C
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:15)

rs_ID	r²[population]
rs13121109	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13127563	1.00[ASN][1000 genomes]
rs1568137	1.00[ASN][1000 genomes]
rs17023180	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17023187	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34877561	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4835408	1.00[ASN][1000 genomes]
rs6537476	1.00[ASN][1000 genomes]
rs6537477	1.00[ASN][1000 genomes]
rs6537478	1.00[ASN][1000 genomes]
rs67538939	1.00[ASN][1000 genomes]
rs6817076	1.00[ASN][1000 genomes]
rs6852395	1.00[ASN][1000 genomes]
rs71616536	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7673178	1.00[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	nsv830108	chr4:148114652-148311104	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region miRNA	3 gene(s)	inside rSNPs	diseases
2	nsv830109	chr4:148295061-148468605	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:148309000-148309800	Enhancers	HMEC	breast
2	chr4:148309000-148310000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr4:148309000-148310600	Weak transcription	Adipose Nuclei	Adipose
4	chr4:148309200-148309800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr4:148309200-148309800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr4:148309200-148309800	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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