Variant report

Variant	rs72669472
Chromosome Location	chr1:67129457-67129458
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10159265	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs10749764	0.87[ASN][1000 genomes]
rs11208940	1.00[ASN][1000 genomes]
rs12094526	0.98[ASN][1000 genomes]
rs13376692	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs17129244	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs17129245	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs17129252	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs17129269	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs17129307	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17440390	0.83[EUR][1000 genomes]
rs2182110	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs55817355	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs55895340	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs58418199	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs61313508	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6588213	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6664403	0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6664597	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6670827	0.98[ASN][1000 genomes]
rs6694782	0.98[ASN][1000 genomes]
rs72669463	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs72669465	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs72669469	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72669475	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72669488	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs74085003	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs74087510	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7536634	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7538967	0.82[EUR][1000 genomes]
rs7540244	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7543378	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7545674	0.84[EUR][1000 genomes]
rs7549727	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[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	nsv869413	chr1:67082512-67414286	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:67090400-67155000	Weak transcription	Fetal Heart	heart
2	chr1:67100000-67144400	Weak transcription	Left Ventricle	heart
3	chr1:67106200-67143000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr1:67108000-67136200	Weak transcription	Fetal Brain Female	brain
5	chr1:67109200-67141800	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr1:67109600-67134200	Weak transcription	Brain Cingulate Gyrus	brain
7	chr1:67109600-67155000	Weak transcription	Brain Anterior Caudate	brain
8	chr1:67110800-67134400	Weak transcription	Brain Substantia Nigra	brain
9	chr1:67111000-67135200	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr1:67111400-67154800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr1:67114200-67134200	Weak transcription	Brain Hippocampus Middle	brain
12	chr1:67114200-67142000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr1:67114200-67156400	Weak transcription	Stomach Smooth Muscle	stomach
14	chr1:67114600-67142200	Weak transcription	NHLF	lung
15	chr1:67118800-67138800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr1:67118800-67140400	Weak transcription	Aorta	Aorta
17	chr1:67121200-67145400	Weak transcription	Brain Angular Gyrus	brain
18	chr1:67122000-67130000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr1:67122000-67141200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr1:67122400-67132600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr1:67126600-67134800	Weak transcription	Fetal Kidney	kidney
22	chr1:67128600-67131000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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