Variant report

Variant	rs9300054
Chromosome Location	chr11:46181091-46181092
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:46179600-46181400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr11:46179600-46181600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr11:46180000-46183000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr11:46180800-46182200	Enhancers	Hela-S3	cervix
5	chr11:46180800-46182200	Enhancers	HMEC	breast
6	chr11:46181000-46181200	Enhancers	Rectal Mucosa Donor 29	rectum
7	chr11:46181000-46181600	Enhancers	Fetal Intestine Large	intestine
8	chr11:46181000-46181600	Enhancers	Placenta	Placenta
9	chr11:46181000-46181800	Enhancers	Placenta Amnion	Placenta Amnion
10	chr11:46181000-46182000	Flanking Active TSS	NHEK	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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