Variant report

Variant	rs10088090
Chromosome Location	chr8:91201219-91201220
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:91193596..91196582-chr8:91200011..91201961,3	K562	blood:
2	chr8:91199087..91202530-chr8:91204069..91207445,5	K562	blood:
3	chr8:91193596..91196355-chr8:91200011..91201961,2	K562	blood:
4	chr8:91200381..91201934-chr8:91204615..91207445,3	K562	blood:

Extended variants
information (count: 32 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10102323	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10113268	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10504892	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10808584	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10956507	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10956509	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12676309	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12676331	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12679792	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12681542	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2107073	0.85[EUR][1000 genomes]
rs28461789	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4961179	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4961180	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4961181	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4961182	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4961183	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4961184	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs58516164	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7815353	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7818663	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7819285	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7823556	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7828848	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs983139	0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758164	chr8:91000786-91329669	Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	esv2759628	chr8:91000786-91329669	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	esv2757281	chr8:91090821-91235335	Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	nsv470225	chr8:91113616-91229254	Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
5	nsv891184	chr8:91114698-91222654	Active TSS Genic enhancers Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
6	esv35109	chr8:91150726-91226940	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	8 gene(s)	inside rSNPs	diseases
7	nsv818643	chr8:91153308-91212148	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers	Chromatin interactive region	8 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	chr8:91200200-91201400	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr8:91200600-91202600	Enhancers	K562	blood

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