Variant report

Variant rs112998509
Chromosome Location chr18:29009286-29009287
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr18:29006600-29010600 Enhancers Placenta Amnion Placenta Amnion
2 chr18:29007200-29010800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr18:29007400-29010800 Enhancers NHEK skin
4 chr18:29008200-29010600 Enhancers Stomach Mucosa stomach
5 chr18:29008200-29010800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr18:29008400-29009800 Enhancers Breast Myoepithelial Primary Cells Breast
7 chr18:29008400-29010600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr18:29008800-29009600 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
9 chr18:29008800-29010600 Enhancers HMEC breast
10 chr18:29009000-29009400 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
11 chr18:29009000-29010400 Enhancers Rectal Mucosa Donor 31 rectum
12 chr18:29009200-29009400 Enhancers Small Intestine intestine
13 chr18:29009200-29010200 Enhancers iPS-15b Cell Line embryonic stem cell
14 chr18:29009200-29010200 Enhancers Fetal Intestine Large intestine
15 chr18:29009200-29010400 Enhancers ES-I3 Cell Line embryonic stem cell
16 chr18:29009200-29010600 Enhancers Hela-S3 cervix

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