Variant report

Variant rs80055261
Chromosome Location chr18:29010166-29010167
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 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 chr18:29008400-29010600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr18:29008800-29010600 Enhancers HMEC breast
8 chr18:29009000-29010400 Enhancers Rectal Mucosa Donor 31 rectum
9 chr18:29009200-29010200 Enhancers iPS-15b Cell Line embryonic stem cell
10 chr18:29009200-29010200 Enhancers Fetal Intestine Large intestine
11 chr18:29009200-29010400 Enhancers ES-I3 Cell Line embryonic stem cell
12 chr18:29009200-29010600 Enhancers Hela-S3 cervix
13 chr18:29009400-29010400 Enhancers HUES6 Cell Line embryonic stem cell
14 chr18:29009600-29010200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
15 chr18:29009800-29010200 Enhancers ES-WA7 Cell Line embryonic stem cell
16 chr18:29009800-29010400 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
17 chr18:29010000-29010200 Enhancers Small Intestine intestine

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