Variant report

Variant	rs58611626
Chromosome Location	chr4:76484479-76484480
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]
rs17000621	1.00[ASN][1000 genomes]
rs17000639	1.00[ASN][1000 genomes]
rs55708633	1.00[ASN][1000 genomes]
rs56806434	1.00[ASN][1000 genomes]
rs6847623	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6856762	1.00[ASN][1000 genomes]
rs73825508	1.00[ASN][1000 genomes]
rs73827648	1.00[ASN][1000 genomes]
rs7676544	1.00[ASN][1000 genomes]
rs7695615	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	nsv594687	chr4:76154064-76502748	Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Enhancers Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
2	nsv534570	chr4:76214619-76498362	ZNF genes & repeats Flanking Active TSS Strong transcription Weak transcription Enhancers Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:76481400-76486800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr4:76481800-76487000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr4:76481800-76487000	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr4:76481800-76487000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr4:76481800-76487000	Weak transcription	HMEC	breast
6	chr4:76481800-76487000	Weak transcription	NHEK	skin
7	chr4:76482200-76487000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr4:76483000-76485000	Weak transcription	Placenta	Placenta

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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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