Variant report

Variant	rs73287338
Chromosome Location	chr12:30672701-30672702
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs12310979	1.00[AMR][1000 genomes]
rs73287354	1.00[AFR][1000 genomes];1.00[AMR][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	esv3343291	chr12:30455597-30992837	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:30669600-30673000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr12:30671400-30672800	Enhancers	Fetal Kidney	kidney
3	chr12:30671400-30673000	Enhancers	HepG2	liver
4	chr12:30671600-30672800	Enhancers	Stomach Mucosa	stomach
5	chr12:30671800-30672800	Enhancers	Fetal Muscle Leg	muscle
6	chr12:30672600-30673000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr12:30672600-30681200	Weak transcription	K562	blood
8	chr12:30672600-30686800	Weak transcription	Ovary	ovary

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

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