Variant report

Variant	rs557254760
Chromosome Location	chr21:16262651-16262652
allele	A/C
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	esv3449026	chr21:16262081-16265479	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:16249200-16264600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr21:16259600-16262800	Enhancers	Fetal Intestine Large	intestine
3	chr21:16260000-16264600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr21:16261200-16263400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr21:16261400-16263000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr21:16261400-16267000	Weak transcription	Fetal Muscle Leg	muscle
7	chr21:16261800-16265200	Weak transcription	Dnd41	blood
8	chr21:16262000-16262800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr21:16262000-16263000	Enhancers	HepG2	liver
10	chr21:16262000-16263400	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr21:16262000-16284200	Weak transcription	Primary hematopoietic stem cells	blood
12	chr21:16262200-16262800	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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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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