Variant report

Variant	rs73029705
Chromosome Location	chr1:158320762-158320763
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs11801650	0.92[AFR][1000 genomes]
rs11801964	0.82[AFR][1000 genomes]
rs11804278	0.90[AFR][1000 genomes]
rs11804812	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11805227	0.81[AFR][1000 genomes]
rs11805538	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11809955	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11810029	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61734681	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73012003	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73012022	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73027868	0.96[AFR][1000 genomes]
rs73027869	0.96[AFR][1000 genomes]
rs73027896	1.00[AMR][1000 genomes]
rs73027898	1.00[AMR][1000 genomes]
rs73027900	0.98[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv999542	chr1:158015715-158368132	Bivalent Enhancer Genic enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv872479	chr1:158118787-158484285	Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv872480	chr1:158153526-158450238	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
4	nsv831692	chr1:158223459-158392016	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv998569	chr1:158317392-158443389	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:158319600-158321600	Enhancers	Dnd41	blood
2	chr1:158319800-158321400	Enhancers	Fetal Thymus	thymus

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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