Variant report

Variant	rs2053855
Chromosome Location	chr15:73164814-73164815
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs2012304	1.00[EUR][1000 genomes]
rs2899810	1.00[EUR][1000 genomes]
rs930662	1.00[EUR][1000 genomes]
rs930663	1.00[EUR][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	nsv482512	chr15:73023099-73175952	Flanking Active TSS Strong transcription Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:73161800-73165600	Enhancers	Skeletal Muscle Male	skeletal muscle
2	chr15:73162600-73165800	Enhancers	Skeletal Muscle Female	skeletal muscle
3	chr15:73162800-73166000	Enhancers	Psoas Muscle	Psoas
4	chr15:73164000-73167400	Enhancers	Fetal Muscle Leg	muscle
5	chr15:73164200-73166200	Enhancers	Fetal Brain Male	brain
6	chr15:73164600-73165000	Enhancers	Fetal Brain Female	brain
7	chr15:73164800-73166000	Weak transcription	Fetal Muscle Trunk	muscle

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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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