Variant report

Variant	rs10137623
Chromosome Location	chr14:39693068-39693069
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr14:39690148..39692016-chr14:39692891..39694587,2	MCF-7	breast:
2	chr14:39581979..39584975-chr14:39691511..39693486,2	MCF-7	breast:
3	chr14:39642456..39648509-chr14:39688590..39693921,7	MCF-7	breast:
4	chr14:39655421..39657718-chr14:39690495..39693068,2	K562	blood:
5	chr14:39651862..39654641-chr14:39690512..39693459,3	K562	blood:

Variant related genes	Relation type
ENSG00000092208	Chromatin interaction
ENSG00000100941	Chromatin interaction
ENSG00000259083	Chromatin interaction

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10144445	0.86[ASN][1000 genomes]
rs11622951	0.88[CHB][hapmap];0.95[JPT][hapmap]
rs12433610	0.94[JPT][hapmap]
rs1570131	0.80[CHB][hapmap]
rs17109030	0.87[CHB][hapmap]
rs17621388	0.87[CHB][hapmap]
rs17692639	0.94[CHB][hapmap]
rs17694832	0.80[CHB][hapmap]
rs1980609	0.94[CHB][hapmap];0.94[JPT][hapmap]
rs1998193	0.88[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2025027	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2025028	0.88[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2164066	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2415537	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs28502509	0.88[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs34664345	0.84[AFR][1000 genomes]
rs34843498	0.94[CHB][hapmap]
rs35305286	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4902459	0.88[CHB][hapmap];0.89[JPT][hapmap]
rs56167516	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6571912	0.88[CHB][hapmap];0.89[JPT][hapmap]
rs6571921	0.88[JPT][hapmap]
rs7141840	0.88[CHB][hapmap];0.94[JPT][hapmap];0.80[ASN][1000 genomes]
rs7143942	0.87[CHB][hapmap]
rs7153074	0.89[JPT][hapmap]
rs7153523	0.82[CHB][hapmap];0.94[JPT][hapmap];0.82[ASN][1000 genomes]
rs7154632	0.94[CHB][hapmap]
rs7155164	0.88[CHB][hapmap]
rs8006182	0.87[CHB][hapmap]
rs8014839	0.80[CHB][hapmap]
rs8019246	0.90[ASN][1000 genomes]
rs8019368	0.93[ASN][1000 genomes]
rs9322996	0.88[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9743804	0.82[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	nsv1246	chr14:39656597-39701520	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Strong transcription	TF binding region Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv1053133	chr14:39657535-39770729	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
3	nsv977619	chr14:39690884-39697666	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:39674000-39705400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr14:39693000-39693200	Enhancers	HepG2	liver

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