Variant report

Variant rs219153
Chromosome Location chr2:33216370-33216371
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:33202600-33225600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
2 chr2:33208000-33218000 Weak transcription Cortex derived primary cultured neurospheres brain
3 chr2:33209000-33217000 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
4 chr2:33209600-33217200 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
5 chr2:33215000-33219400 Enhancers Fetal Heart heart
6 chr2:33215200-33216800 Weak transcription Right Ventricle heart
7 chr2:33215800-33216400 Enhancers Fetal Stomach stomach
8 chr2:33215800-33216800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr2:33215800-33217200 Enhancers Duodenum Smooth Muscle Duodenum
10 chr2:33216000-33216600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr2:33216000-33216600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
12 chr2:33216000-33216600 Enhancers Colon Smooth Muscle Colon
13 chr2:33216000-33217000 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
14 chr2:33216200-33217200 Weak transcription HMEC breast
15 chr2:33216200-33217400 Enhancers K562 blood
16 chr2:33216200-33218000 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived

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