Variant report

Variant	rs28550691
Chromosome Location	chr4:82100138-82100139
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10033237	0.89[EUR][1000 genomes]
rs1078980	0.87[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs11722019	0.87[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs11722928	0.88[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs11722958	0.84[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs11736177	0.87[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs11941243	0.80[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs1348399	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1982283	0.87[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs2102818	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs3733553	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs58629505	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6846241	0.92[EUR][1000 genomes]
rs751295	0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs7687935	0.80[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs7688672	0.80[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs7696645	0.80[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs9992933	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv999729	chr4:81802554-82627820	Genic enhancers Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv537156	chr4:81802554-82627820	Flanking Active TSS Strong transcription Enhancers Weak transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv829984	chr4:81979988-82113977	Flanking Active TSS Enhancers Strong transcription Active TSS Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
4	esv1822437	chr4:82025743-82118996	Strong transcription Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:82086600-82104800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr4:82088000-82113800	Weak transcription	Fetal Intestine Large	intestine
3	chr4:82088200-82114400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr4:82090600-82104400	Weak transcription	Fetal Intestine Small	intestine
5	chr4:82093600-82115400	Weak transcription	NHDF-Ad	bronchial
6	chr4:82099600-82100600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr4:82099600-82100800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr4:82100000-82105800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr4:82100000-82117200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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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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