Variant report

Variant	rs10183153
Chromosome Location	chr2:37394435-37394436
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Variant related genes	Relation type
ENSG00000138068	Chromatin interaction
ENSG00000218739	Chromatin interaction
ENSG00000224891	Chromatin interaction
ENSG00000055332	Chromatin interaction

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:37394400-37394600	Enhancers	Fetal Intestine Large	intestine
2	chr2:37394400-37395000	Enhancers	Stomach Mucosa	stomach
3	chr2:37394400-37395200	Enhancers	Duodenum Mucosa	Duodenum
4	chr2:37394400-37395600	Enhancers	Fetal Intestine Small	intestine

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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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