Variant report

Variant	rs1254851
Chromosome Location	chr10:44418024-44418025
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs10793506	0.82[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	nsv1051921	chr10:44378011-44458880	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 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	chr10:44406800-44421800	Weak transcription	Fetal Heart	heart
2	chr10:44408200-44424000	Weak transcription	Right Ventricle	heart
3	chr10:44417400-44418200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
4	chr10:44417400-44418200	Enhancers	Lung	lung
5	chr10:44417600-44418600	Enhancers	Spleen	Spleen
6	chr10:44417600-44419400	Enhancers	Skeletal Muscle Male	skeletal muscle
7	chr10:44417800-44418200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
8	chr10:44417800-44418200	Enhancers	Left Ventricle	heart
9	chr10:44417800-44418200	Enhancers	Right Atrium	heart

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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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