Variant report

Variant	rs17884120
Chromosome Location	chr11:102661518-102661519
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:102651600-102667600	Weak transcription	NHDF-Ad	bronchial
2	chr11:102655600-102668600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr11:102657200-102667600	Weak transcription	Fetal Intestine Small	intestine
4	chr11:102657400-102664400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr11:102657400-102665200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr11:102659600-102661600	Weak transcription	Stomach Mucosa	stomach
7	chr11:102659600-102664600	Weak transcription	Fetal Stomach	stomach
8	chr11:102660200-102662400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr11:102660400-102662600	Weak transcription	NHEK	skin
10	chr11:102660600-102661800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr11:102661200-102662000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr11:102661200-102662200	Strong transcription	NHLF	lung

Quick Search:

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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