Variant report

Variant rs145121277
Chromosome Location chr5:60148794-60148795
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:60147600-60149200 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
2 chr5:60147800-60149000 Enhancers Fetal Intestine Small intestine
3 chr5:60147800-60149000 Enhancers Placenta Placenta
4 chr5:60147800-60149200 Enhancers Fetal Intestine Large intestine
5 chr5:60147800-60149600 Enhancers K562 blood
6 chr5:60148000-60148800 Bivalent Enhancer hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
7 chr5:60148000-60149000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr5:60148000-60149200 Enhancers HUES6 Cell Line embryonic stem cell
9 chr5:60148000-60149400 Enhancers ES-I3 Cell Line embryonic stem cell
10 chr5:60148200-60148800 Enhancers ES-UCSF4 Cell Line embryonic stem cell
11 chr5:60148200-60149000 Enhancers ES-WA7 Cell Line embryonic stem cell
12 chr5:60148200-60149200 Enhancers HUES48 Cell Line embryonic stem cell
13 chr5:60148400-60148800 Enhancers iPS-20b Cell Line embryonic stem cell
14 chr5:60148400-60149000 Enhancers H1 Cell Line embryonic stem cell
15 chr5:60148400-60149000 Enhancers iPS-15b Cell Line embryonic stem cell
16 chr5:60148400-60149600 Enhancers HUES64 Cell Line embryonic stem cell

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