Variant report

Variant	rs7525103
Chromosome Location	chr1:221391786-221391787
allele	G/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:9)

rs_ID	r²[population]
rs7522887	1.00[ASN][1000 genomes]
rs7536615	1.00[ASN][1000 genomes]
rs9431075	1.00[ASN][1000 genomes]
rs9431077	1.00[ASN][1000 genomes]
rs9431078	1.00[ASN][1000 genomes]
rs9431080	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9431084	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9431442	1.00[ASN][1000 genomes]
rs9431450	0.83[AFR][1000 genomes];1.00[AMR][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	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:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:221390200-221391800	Enhancers	Fetal Muscle Leg	muscle
2	chr1:221390200-221392000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr1:221390200-221392000	Enhancers	Muscle Satellite Cultured Cells	--
4	chr1:221390200-221392400	Enhancers	Osteobl	bone
5	chr1:221390400-221392400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr1:221390600-221392400	Enhancers	NHDF-Ad	bronchial
7	chr1:221390800-221391800	Enhancers	Adipose Nuclei	Adipose
8	chr1:221391000-221391800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr1:221391000-221391800	Enhancers	Skeletal Muscle Male	skeletal muscle
10	chr1:221391000-221392200	Weak transcription	NHLF	lung
11	chr1:221391200-221392200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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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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