Variant report

Variant	rs557905774
Chromosome Location	chr10:93306808-93306809
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 1 )
Associated
traits (count: 0)

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	esv19622	chr10:93305214-93361590	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:93296200-93312200	Weak transcription	Psoas Muscle	Psoas
2	chr10:93297000-93311400	Weak transcription	Brain Cingulate Gyrus	brain
3	chr10:93297000-93311400	Weak transcription	Left Ventricle	heart
4	chr10:93299400-93311400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr10:93301000-93314800	Weak transcription	Aorta	Aorta
6	chr10:93302400-93311400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr10:93302600-93308000	Weak transcription	Fetal Brain Male	brain
8	chr10:93302600-93312000	Weak transcription	NHLF	lung
9	chr10:93302800-93307800	Weak transcription	Hela-S3	cervix
10	chr10:93304800-93308200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr10:93305800-93311400	Weak transcription	Skeletal Muscle Female	skeletal muscle
12	chr10:93306400-93312200	Weak transcription	Pancreas	Pancrea
13	chr10:93306600-93308000	Weak transcription	Fetal Lung	lung

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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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