Variant report

Variant	rs1775989
Chromosome Location	chr1:86177917-86177918
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs1094360	0.82[AFR][1000 genomes]
rs12037294	0.85[ASN][1000 genomes]
rs12758966	0.85[ASN][1000 genomes]
rs1481200	0.90[AFR][1000 genomes];0.87[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs1617458	0.86[ASN][1000 genomes]
rs17128293	0.93[ASN][1000 genomes]
rs1764287	0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs1764295	0.84[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs1775985	0.84[AFR][1000 genomes];0.84[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs1775986	0.84[AFR][1000 genomes];0.84[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs1775987	0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs1775992	0.85[ASN][1000 genomes]
rs1775993	0.85[ASN][1000 genomes]
rs2014733	0.87[AFR][1000 genomes];0.87[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs2389973	0.90[AFR][1000 genomes];0.87[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs2389974	0.80[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs2970548	0.85[ASN][1000 genomes]
rs313723	0.84[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs313724	0.84[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs313725	0.93[ASN][1000 genomes]
rs399547	0.89[AFR][1000 genomes];0.84[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs429040	0.93[ASN][1000 genomes]
rs4379699	0.93[ASN][1000 genomes]
rs444875	0.93[ASN][1000 genomes]
rs6686719	0.89[AFR][1000 genomes];0.84[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs7521240	0.93[ASN][1000 genomes]
rs821378	0.85[ASN][1000 genomes]
rs821380	0.85[ASN][1000 genomes]
rs821382	0.85[ASN][1000 genomes]
rs821383	0.85[ASN][1000 genomes]
rs821385	0.81[AMR][1000 genomes]
rs821387	0.82[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs821388	0.80[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs821390	0.85[ASN][1000 genomes]
rs821397	0.82[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs821400	0.82[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs821403	0.85[ASN][1000 genomes]
rs821404	0.85[ASN][1000 genomes]
rs849158	0.82[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs9324152	0.85[ASN][1000 genomes]
rs9651138	0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs9661608	0.82[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs9661951	0.82[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs9701898	0.82[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs9793556	0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1006994	chr1:85454304-86327679	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
2	esv3391173	chr1:86005637-86337469	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
3	nsv817212	chr1:86127851-86658426	Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv871471	chr1:86143084-86211516	Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:86174400-86185800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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