Variant report

Variant	rs17879947
Chromosome Location	chr11:102662740-102662741
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:14 , 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	chr11:102659600-102664600	Weak transcription	Fetal Stomach	stomach
7	chr11:102662000-102667600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr11:102662200-102668400	Weak transcription	NHLF	lung
9	chr11:102662400-102662800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr11:102662400-102662800	Enhancers	HMEC	breast
11	chr11:102662400-102663000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr11:102662600-102662800	Weak transcription	Stomach Mucosa	stomach
13	chr11:102662600-102663000	Enhancers	NHEK	skin
14	chr11:102662600-102664600	Weak transcription	HUVEC	blood vessel

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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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