Variant report

Variant	rs35997606
Chromosome Location	chr2:190358689-190358690
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10187060	0.85[ASN][1000 genomes]
rs10497700	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10497703	0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10755004	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10931416	0.83[ASN][1000 genomes]
rs10931418	0.84[ASN][1000 genomes]
rs10931419	0.84[ASN][1000 genomes]
rs1112578	0.83[ASN][1000 genomes]
rs1157910	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11677066	0.83[ASN][1000 genomes]
rs11688021	0.84[ASN][1000 genomes]
rs11695159	0.80[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12612412	0.80[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12613876	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12616234	0.83[ASN][1000 genomes]
rs12623723	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12987962	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12988143	0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12990035	0.82[ASN][1000 genomes]
rs12990235	0.83[ASN][1000 genomes]
rs12997620	0.80[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13010531	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13015203	0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13032853	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13033841	0.84[ASN][1000 genomes]
rs1402368	0.80[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1520855	0.80[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1520857	0.80[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1520864	0.83[ASN][1000 genomes]
rs1581351	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2119069	0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2304703	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4287797	0.84[ASN][1000 genomes]
rs4667281	0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6728055	0.84[ASN][1000 genomes]
rs6745108	0.84[ASN][1000 genomes]
rs7419276	0.86[ASN][1000 genomes]
rs7588453	0.83[ASN][1000 genomes]
rs7593821	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7596592	0.84[ASN][1000 genomes]
rs963738	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9679659	0.82[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	nsv533029	chr2:189812229-190554339	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
2	nsv875615	chr2:190215527-190444392	Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
3	nsv584062	chr2:190272195-190376493	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	19 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	chr2:190335000-190366200	Weak transcription	Ovary	ovary
2	chr2:190349200-190365000	Weak transcription	Fetal Intestine Large	intestine
3	chr2:190353000-190364600	Weak transcription	Skeletal Muscle Female	skeletal muscle

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