Variant report

Variant rs73023431
Chromosome Location chr2:173275503-173275504
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:173267600-173275600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
2 chr2:173270000-173277600 Weak transcription Cortex derived primary cultured neurospheres brain
3 chr2:173270400-173277600 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
4 chr2:173271000-173275800 Enhancers HMEC breast
5 chr2:173272800-173276400 Enhancers HUVEC blood vessel
6 chr2:173273400-173277600 Weak transcription Adipose Nuclei Adipose
7 chr2:173273400-173278000 Weak transcription Left Ventricle heart
8 chr2:173273400-173280600 Weak transcription Fetal Intestine Small intestine
9 chr2:173273600-173277400 Weak transcription Thymus Thymus
10 chr2:173274000-173281000 Weak transcription Fetal Kidney kidney
11 chr2:173274600-173277800 Weak transcription Pancreas Pancrea
12 chr2:173274600-173290200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr2:173274800-173280000 Weak transcription Stomach Mucosa stomach
14 chr2:173275400-173275600 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived

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