Variant report

Variant rs62174645
Chromosome Location chr2:173820572-173820573
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:173800600-173829400 Weak transcription Cortex derived primary cultured neurospheres brain
2 chr2:173807800-173831600 Weak transcription Left Ventricle heart
3 chr2:173816600-173831800 Weak transcription Lung lung
4 chr2:173816800-173821600 Weak transcription Fetal Thymus thymus
5 chr2:173817200-173821600 Weak transcription Thymus Thymus
6 chr2:173819200-173827000 Weak transcription NHLF lung
7 chr2:173819400-173821000 Enhancers Placenta Amnion Placenta Amnion
8 chr2:173819600-173820800 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
9 chr2:173819600-173826800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr2:173819800-173820800 Enhancers ES-UCSF4 Cell Line embryonic stem cell
11 chr2:173819800-173826800 Weak transcription NHEK skin
12 chr2:173820400-173820600 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
13 chr2:173820400-173820600 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
14 chr2:173820400-173820600 Enhancers H9 Cell Line embryonic stem cell

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