Variant report

Variant	rs73349693
Chromosome Location	chr12:74980638-74980639
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs1493814	0.82[ASN][1000 genomes]
rs1493815	0.82[ASN][1000 genomes]
rs1493816	0.82[ASN][1000 genomes]
rs1493817	0.82[ASN][1000 genomes]
rs1493831	0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1493833	0.95[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1493834	0.95[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17113566	0.92[ASN][1000 genomes]
rs17113587	0.92[ASN][1000 genomes]
rs1903420	1.00[ASN][1000 genomes]
rs2605371	0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2641483	0.95[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2641487	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2641505	0.82[ASN][1000 genomes]
rs2641506	0.82[ASN][1000 genomes]
rs2934408	0.92[ASN][1000 genomes]
rs7973277	0.92[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	nsv1039468	chr12:74080586-75000246	Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv899293	chr12:74835107-74995760	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA target site	5 gene(s)	inside rSNPs	diseases
3	nsv899295	chr12:74854750-74984992	Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:74979800-74980800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr12:74980000-74980800	Enhancers	Brain Cingulate Gyrus	brain
3	chr12:74980000-74980800	Enhancers	Stomach Mucosa	stomach
4	chr12:74980000-74981000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
5	chr12:74980200-74980800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr12:74980200-74980800	Enhancers	Brain Anterior Caudate	brain
7	chr12:74980200-74980800	Enhancers	Brain Hippocampus Middle	brain
8	chr12:74980400-74980800	Enhancers	Brain Substantia Nigra	brain
9	chr12:74980600-74981000	Enhancers	Brain Inferior Temporal Lobe	brain

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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