Variant report

Variant	rs60583234
Chromosome Location	chr8:54132452-54132453
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs1425908	0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs16918842	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs58882388	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][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	nsv1016224	chr8:53719941-54367534	Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv530534	chr8:53787984-54367353	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	esv3377304	chr8:53873441-54380875	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:54127600-54136400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr8:54130600-54135600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr8:54131600-54135800	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr8:54131800-54135800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr8:54131800-54136000	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr8:54131800-54136000	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr8:54131800-54136400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr8:54132000-54135800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr8:54132000-54135800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr8:54132000-54136400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr8:54132000-54141600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr8:54132000-54149400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr8:54132200-54135600	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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