Variant report

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10081574	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10087822	0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10102760	0.91[EUR][1000 genomes]
rs10103936	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10108200	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10109496	0.91[EUR][1000 genomes]
rs10111415	0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12543541	0.90[EUR][1000 genomes]
rs12548242	0.85[EUR][1000 genomes]
rs16888856	0.84[CHB][hapmap];0.83[EUR][1000 genomes]
rs16888858	0.85[EUR][1000 genomes]
rs16888859	0.84[CHB][hapmap];0.85[EUR][1000 genomes]
rs17664177	0.85[CHB][hapmap];0.85[EUR][1000 genomes]
rs28538786	0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs28544915	0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs28839812	0.90[EUR][1000 genomes]
rs56203264	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs56777536	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6981455	0.85[EUR][1000 genomes]
rs6981584	0.85[EUR][1000 genomes]
rs6981928	0.85[EUR][1000 genomes]
rs7016030	0.87[ASN][1000 genomes]
rs7812602	0.85[EUR][1000 genomes]
rs7824282	0.85[CHB][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[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	nsv530386	chr8:117509968-118391406	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
2	nsv831434	chr8:117784467-117977825	Flanking Active TSS Genic enhancers Weak transcription Enhancers Active TSS Bivalent/Poised TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
3	nsv1034015	chr8:117790928-117843979	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Active TSS	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:117839400-117844400	Weak transcription	Psoas Muscle	Psoas
2	chr8:117840600-117845800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr8:117840800-117859400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr8:117841000-117843600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr8:117841000-117856800	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr8:117841600-117845200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr8:117841600-117845400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr8:117842200-117845200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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