Variant report

Variant	rs10836121
Chromosome Location	chr11:33869713-33869714
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

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	nsv526555	chr11:33868607-33886294	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs10836121	CD59	Cis_1M	lymphoblastoid	RTeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:33864400-33872400	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr11:33864400-33874000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr11:33864400-33874200	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr11:33864800-33880600	Weak transcription	Brain Anterior Caudate	brain
5	chr11:33867200-33878000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr11:33869200-33874000	Weak transcription	Adipose Nuclei	Adipose

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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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