Variant report

Variant rs60513343
Chromosome Location chr2:181899590-181899591
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:181857800-181901200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
2 chr2:181873400-181901000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr2:181886000-181901200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
4 chr2:181890800-181901200 Weak transcription Primary T helper cells PMA-I stimulated --
5 chr2:181893400-181901200 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr2:181895000-181904000 Weak transcription Left Ventricle heart
7 chr2:181897000-181900600 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
8 chr2:181897400-181901400 Weak transcription NH-A brain
9 chr2:181897600-181901600 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
10 chr2:181898400-181900800 Weak transcription Osteobl bone

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