Variant report

Variant	rs16996408
Chromosome Location	chr21:39907728-39907729
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:39896000-39910400	Weak transcription	Small Intestine	intestine
2	chr21:39904200-39910400	Weak transcription	Aorta	Aorta
3	chr21:39904400-39909000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr21:39904800-39910800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr21:39905200-39908000	Weak transcription	HepG2	liver
6	chr21:39906000-39910400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	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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