Variant report

Variant rs4485444
Chromosome Location chr18:29009076-29009077
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr18:29004400-29009200 Weak transcription ES-I3 Cell Line embryonic stem cell
2 chr18:29006600-29010600 Enhancers Placenta Amnion Placenta Amnion
3 chr18:29007200-29010800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr18:29007400-29010800 Enhancers NHEK skin
5 chr18:29008200-29010600 Enhancers Stomach Mucosa stomach
6 chr18:29008200-29010800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr18:29008400-29009800 Enhancers Breast Myoepithelial Primary Cells Breast
8 chr18:29008400-29010600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr18:29008800-29009600 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
10 chr18:29008800-29010600 Enhancers HMEC breast
11 chr18:29009000-29009400 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
12 chr18:29009000-29010400 Enhancers Rectal Mucosa Donor 31 rectum

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