Variant report

Variant	rs7827802
Chromosome Location	chr8:121153704-121153705
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs58252479	1.00[AMR][1000 genomes]
rs59400707	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60163884	1.00[AMR][1000 genomes]
rs60298200	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61179468	1.00[AMR][1000 genomes]
rs61396869	1.00[AMR][1000 genomes]
rs73704242	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7846067	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7846510	1.00[AFR][1000 genomes];1.00[AMR][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	nsv891418	chr8:120600965-121301474	Active TSS Flanking Active TSS Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
2	esv3348294	chr8:121000288-121250984	Flanking Active TSS Strong transcription Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS Active 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	6 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	chr8:121152400-121153800	Enhancers	Fetal Lung	lung
2	chr8:121152400-121165400	Weak transcription	Ovary	ovary
3	chr8:121153000-121153800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr8:121153000-121155000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr8:121153200-121154600	Enhancers	Aorta	Aorta
6	chr8:121153400-121153800	Enhancers	NHLF	lung
7	chr8:121153600-121154000	Enhancers	Fetal Stomach	stomach
8	chr8:121153600-121154400	Enhancers	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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