Variant report

Variant rs17166643
Chromosome Location chr7:13076721-13076722
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:13072000-13082200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr7:13072400-13080600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
3 chr7:13073800-13076800 Weak transcription Rectal Smooth Muscle rectum
4 chr7:13074600-13082600 Weak transcription H9 Cell Line embryonic stem cell
5 chr7:13075200-13078600 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
6 chr7:13075400-13078600 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
7 chr7:13076600-13077000 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
8 chr7:13076600-13084200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin

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