Variant report

Variant	rs1124757
Chromosome Location	chr1:185732229-185732230
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 75 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:72)

rs_ID	r²[population]
rs11579889	0.83[ASN][1000 genomes]
rs11581777	0.86[EUR][1000 genomes]
rs11583092	0.83[ASN][1000 genomes]
rs11583867	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11807146	0.82[EUR][1000 genomes]
rs12057982	0.90[EUR][1000 genomes]
rs12063964	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12078015	0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12079064	0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12083564	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12085167	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12087032	0.81[EUR][1000 genomes]
rs12098116	0.83[EUR][1000 genomes]
rs1321668	0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1321669	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1321670	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1322359	0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1322362	0.92[EUR][1000 genomes]
rs1322364	0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13374445	0.83[EUR][1000 genomes]
rs1407429	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1407430	0.81[EUR][1000 genomes]
rs1407431	0.81[EUR][1000 genomes]
rs1552281	0.94[ASN][1000 genomes]
rs16824390	0.83[ASN][1000 genomes]
rs16824396	0.83[ASN][1000 genomes]
rs16824516	0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs16824564	0.90[EUR][1000 genomes]
rs16824576	0.91[EUR][1000 genomes]
rs17445778	0.83[ASN][1000 genomes]
rs17446906	0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs17447869	0.89[EUR][1000 genomes]
rs17448202	0.87[EUR][1000 genomes]
rs17448216	0.87[EUR][1000 genomes]
rs17448230	0.89[EUR][1000 genomes]
rs17505819	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17507170	0.87[EUR][1000 genomes]
rs2057381	0.87[EUR][1000 genomes]
rs2057383	0.90[EUR][1000 genomes]
rs2057384	0.90[EUR][1000 genomes]
rs2057385	0.87[EUR][1000 genomes]
rs2129125	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2170859	0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2220128	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35314812	0.82[EUR][1000 genomes]
rs35425624	0.94[ASN][1000 genomes]
rs41458549	0.87[EUR][1000 genomes]
rs4515745	0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4593772	0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4596837	0.94[ASN][1000 genomes]
rs4651287	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4651288	0.91[EUR][1000 genomes]
rs57398679	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57686227	0.89[EUR][1000 genomes]
rs61290318	0.82[ASN][1000 genomes]
rs61829860	0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs61831470	0.83[ASN][1000 genomes]
rs61831483	0.83[ASN][1000 genomes]
rs61831485	0.83[ASN][1000 genomes]
rs61831486	0.83[ASN][1000 genomes]
rs61831502	0.83[ASN][1000 genomes]
rs61831503	0.83[ASN][1000 genomes]
rs61831505	0.83[ASN][1000 genomes]
rs61831519	0.82[ASN][1000 genomes]
rs61831528	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs61831532	0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6660510	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6692479	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7414598	0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7544533	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9628625	0.81[EUR][1000 genomes]
rs994970	0.82[AFR][1000 genomes];0.83[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	nsv548398	chr1:185136458-186003094	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	69 gene(s)	inside rSNPs	diseases
2	esv3424090	chr1:185679718-186270877	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
3	esv2753636	chr1:185706947-185734487	Genic enhancers Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:185721800-185736400	Weak transcription	Fetal Lung	lung
2	chr1:185730200-185745000	Weak transcription	Fetal Kidney	kidney
3	chr1:185732000-185733200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr1:185732200-185732400	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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