Variant report

Variant	rs72987308
Chromosome Location	chr3:140903290-140903291
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs11712839	0.85[EUR][1000 genomes]
rs16851087	0.83[ASN][1000 genomes]
rs17282759	0.83[ASN][1000 genomes]
rs1877224	0.83[ASN][1000 genomes]
rs1949113	1.00[ASN][1000 genomes]
rs4308250	0.84[AFR][1000 genomes]
rs56117886	0.83[ASN][1000 genomes]
rs56191597	1.00[ASN][1000 genomes]
rs57028844	0.83[ASN][1000 genomes]
rs57931409	0.83[ASN][1000 genomes]
rs60710013	0.83[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	nsv877550	chr3:140867094-140933231	Weak transcription Enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs72987308	ACPL2	cis	Thyroid	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:140898200-140906000	Weak transcription	Fetal Muscle Trunk	muscle
2	chr3:140901600-140903400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr3:140902800-140904000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr3:140903000-140903800	Enhancers	NHEK	skin

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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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