Variant report

Variant	rs11955150
Chromosome Location	chr5:125047659-125047660
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs11950923	0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11954141	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11955142	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1490976	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1490981	0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs17153120	0.86[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs17153142	0.88[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs17153195	0.96[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs17153198	0.96[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2101603	0.81[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs28684625	0.86[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs34407148	0.81[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs35380838	0.85[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs35762924	0.81[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs62385960	0.81[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs62385965	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs62385966	0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs62385967	0.86[AMR][1000 genomes];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66490821	0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6865600	0.96[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6883544	0.85[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs7707067	0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7723274	0.86[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs902593	0.97[AFR][1000 genomes];0.84[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs989983	0.82[AMR][1000 genomes];0.91[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	nsv1030992	chr5:124708549-125391503	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv537892	chr5:124708549-125391503	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv534468	chr5:124943170-125634960	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:125021800-125055400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr5:125040000-125048600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr5:125043200-125048200	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr5:125043200-125048600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr5:125045000-125050000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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