Variant report

Variant	rs2014178
Chromosome Location	chr3:25458936-25458937
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs1351781	0.97[EUR][1000 genomes]
rs1483826	0.86[EUR][1000 genomes]
rs1483827	0.86[EUR][1000 genomes]
rs1897500	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1897501	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1991788	0.91[EUR][1000 genomes]
rs1994176	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2364118	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4681021	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4681023	0.82[EUR][1000 genomes]
rs7615918	0.93[AMR][1000 genomes];0.97[EUR][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	nsv949035	chr3:25194301-26084890	Weak transcription Bivalent/Poised TSS Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers 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	68 gene(s)	inside rSNPs	diseases
2	nsv834645	chr3:25363723-25555107	Flanking Active TSS Enhancers Weak transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:25453400-25460600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr3:25454000-25462600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr3:25458400-25462200	Weak transcription	Fetal Intestine Large	intestine

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

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