Variant report

Variant rs16883628
Chromosome Location chr8:113471247-113471248
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:113469000-113472600 Enhancers Fetal Intestine Large intestine
2 chr8:113469600-113475000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr8:113470000-113472000 Enhancers A549 lung
4 chr8:113470000-113475600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr8:113470200-113472000 Weak transcription Stomach Mucosa stomach
6 chr8:113470400-113472600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
7 chr8:113470800-113472800 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
8 chr8:113471000-113471600 Enhancers Brain Angular Gyrus brain
9 chr8:113471000-113471600 Enhancers Brain Germinal Matrix brain
10 chr8:113471000-113472000 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
11 chr8:113471000-113472400 Enhancers Brain Substantia Nigra brain
12 chr8:113471000-113472600 Enhancers Brain Hippocampus Middle brain
13 chr8:113471000-113472600 Enhancers Fetal Intestine Small intestine
14 chr8:113471200-113472200 Weak transcription Rectal Smooth Muscle rectum

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