Variant report

Variant	rs35131031
Chromosome Location	chr2:73354286-73354287
allele	C/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:48)

rs_ID	r²[population]
rs10174548	0.83[ASN][1000 genomes]
rs10180995	0.82[ASN][1000 genomes]
rs10865396	0.96[ASN][1000 genomes]
rs11126389	0.96[ASN][1000 genomes]
rs11126390	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11686557	0.90[ASN][1000 genomes]
rs11693673	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11885522	0.86[ASN][1000 genomes]
rs12104691	0.82[ASN][1000 genomes]
rs12614059	0.93[ASN][1000 genomes]
rs13018842	0.81[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs13019020	0.84[ASN][1000 genomes]
rs13385994	0.81[ASN][1000 genomes]
rs13391532	0.86[ASN][1000 genomes]
rs13400920	0.89[ASN][1000 genomes]
rs13416407	0.82[ASN][1000 genomes]
rs1430349	0.89[ASN][1000 genomes]
rs1430350	0.86[ASN][1000 genomes]
rs1430351	0.86[ASN][1000 genomes]
rs1864488	0.88[ASN][1000 genomes]
rs2060002	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs3813222	0.82[ASN][1000 genomes]
rs3901273	0.83[ASN][1000 genomes]
rs4591365	0.86[ASN][1000 genomes]
rs4852908	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs55894650	0.81[ASN][1000 genomes]
rs57701326	0.86[ASN][1000 genomes]
rs57726945	0.88[ASN][1000 genomes]
rs6546800	0.82[ASN][1000 genomes]
rs6546801	0.88[ASN][1000 genomes]
rs6710755	0.88[ASN][1000 genomes]
rs6712925	0.82[ASN][1000 genomes]
rs6727919	0.82[ASN][1000 genomes]
rs6736153	0.83[ASN][1000 genomes]
rs727470	0.83[ASN][1000 genomes]
rs727471	0.83[ASN][1000 genomes]
rs7557173	0.83[ASN][1000 genomes]
rs7559074	0.86[ASN][1000 genomes]
rs7559340	0.83[ASN][1000 genomes]
rs7567413	0.84[ASN][1000 genomes]
rs7570459	0.84[ASN][1000 genomes]
rs7593322	0.86[ASN][1000 genomes]
rs7596830	0.84[ASN][1000 genomes]
rs7599657	0.86[ASN][1000 genomes]
rs7602651	0.89[ASN][1000 genomes]
rs891432	0.81[ASN][1000 genomes]
rs891433	0.82[ASN][1000 genomes]
rs9309471	0.84[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1006801	chr2:73305056-73431711	Weak transcription Active TSS Genic enhancers Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 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	chr2:73345600-73356200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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