Variant report

Variant rs60143052
Chromosome Location chr2:39429905-39429906
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:39411000-39448400 Weak transcription HSMMtube muscle
2 chr2:39419000-39455600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
3 chr2:39423400-39470800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr2:39429400-39431400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
5 chr2:39429600-39430000 Enhancers HUES48 Cell Line embryonic stem cell
6 chr2:39429600-39430000 Enhancers HUES64 Cell Line embryonic stem cell
7 chr2:39429600-39430000 Enhancers iPS-20b Cell Line embryonic stem cell
8 chr2:39429600-39431800 Enhancers iPS-18 Cell Line embryonic stem cell
9 chr2:39429800-39430000 Enhancers HUES6 Cell Line embryonic stem cell
10 chr2:39429800-39430400 Enhancers Cortex derived primary cultured neurospheres brain
11 chr2:39429800-39430600 Flanking Active TSS ES-I3 Cell Line embryonic stem cell
12 chr2:39429800-39431000 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
13 chr2:39429800-39431000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
14 chr2:39429800-39431200 Enhancers iPS-15b Cell Line embryonic stem cell
15 chr2:39429800-39459600 Weak transcription HSMM muscle

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