Variant report

Variant	rs8010219
Chromosome Location	chr14:81696982-81696983
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:81695496..81699679-chr14:81700603..81703669,3	K562	blood:

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10149681	0.93[ASN][1000 genomes]
rs12147118	0.92[ASN][1000 genomes]
rs12586249	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs12590764	0.97[ASN][1000 genomes]
rs1864169	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1951616	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1957546	0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2099108	0.92[ASN][1000 genomes]
rs2288498	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs28890880	0.91[ASN][1000 genomes]
rs4363794	0.92[ASN][1000 genomes]
rs4640110	0.84[EUR][1000 genomes]
rs4899786	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7142641	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7144005	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7148100	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7149294	0.80[AMR][1000 genomes]
rs7149672	0.92[ASN][1000 genomes]
rs7160599	0.80[AMR][1000 genomes]
rs8004096	0.94[ASN][1000 genomes]
rs8006036	0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs8007841	0.91[ASN][1000 genomes]
rs8009888	0.82[AMR][1000 genomes]
rs8011097	0.97[ASN][1000 genomes]
rs8014406	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8016352	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs8016982	0.96[ASN][1000 genomes]
rs8021125	0.97[ASN][1000 genomes]
rs8021385	0.97[ASN][1000 genomes]
rs9806020	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9806027	0.91[ASN][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	nsv832841	chr14:81588322-81743921	Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	86 gene(s)	inside rSNPs	diseases
2	nsv902118	chr14:81679650-81715989	Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	84 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:81688200-81704800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr14:81688800-81700600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr14:81689400-81700600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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