Variant report

Variant	rs257911
Chromosome Location	chr5:128417417-128417418
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr5:128411619..128415483-chr5:128416564..128419080,4	K562	blood:
2	chr5:128416559..128421952-chr5:128424796..128432274,19	K562	blood:
3	chr5:128416535..128420091-chr5:128429855..128432318,3	MCF-7	breast:
4	chr5:128416447..128420070-chr5:128432827..128437106,4	K562	blood:
5	chr5:128373872..128376064-chr5:128416925..128419708,2	K562	blood:

Variant related genes	Relation type
ENSG00000264563	Chromatin interaction
ENSG00000066583	Chromatin interaction

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10036277	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10071265	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1127827	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1181955	0.81[EUR][1000 genomes]
rs11960471	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs13181777	0.80[EUR][1000 genomes]
rs2112697	0.80[AMR][1000 genomes]
rs2161403	0.80[AMR][1000 genomes]
rs2312251	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2430194	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2430195	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs257912	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs257919	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs3798115	0.93[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs3798116	0.93[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs3798117	0.93[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs3798120	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs3822830	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs3822832	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4141014	0.81[EUR][1000 genomes]
rs4836444	0.82[AMR][1000 genomes]
rs58498861	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6595879	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6867600	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6868228	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6871	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6881138	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6888909	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7714427	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs963677	0.81[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv882840	chr5:128205828-128428962	Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv830485	chr5:128298622-128480492	Enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
3	nsv882842	chr5:128301971-128552706	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
4	nsv599701	chr5:128328165-128773052	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases
5	nsv1015525	chr5:128335133-128443859	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	12 gene(s)	inside rSNPs	diseases
6	nsv882846	chr5:128345803-128428962	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv882847	chr5:128368505-128665719	Active TSS Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
8	nsv882848	chr5:128378225-128516629	Strong transcription Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 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	chr5:128409200-128418000	Weak transcription	Fetal Lung	lung
2	chr5:128415800-128418200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr5:128416600-128417600	Enhancers	K562	blood

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