Variant report

Variant rs35969054
Chromosome Location chr4:189320446-189320447
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:189317400-189321200 Weak transcription Brain Inferior Temporal Lobe brain
2 chr4:189319800-189321000 Enhancers H9 Cell Line embryonic stem cell
3 chr4:189320000-189321000 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
4 chr4:189320000-189321600 Enhancers iPS-20b Cell Line embryonic stem cell
5 chr4:189320000-189322400 Enhancers iPS-15b Cell Line embryonic stem cell
6 chr4:189320000-189322600 Enhancers H1 Cell Line embryonic stem cell
7 chr4:189320000-189322600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
8 chr4:189320000-189323000 Enhancers iPS-18 Cell Line embryonic stem cell
9 chr4:189320000-189323200 Enhancers ES-I3 Cell Line embryonic stem cell
10 chr4:189320000-189323200 Enhancers HUES48 Cell Line embryonic stem cell
11 chr4:189320200-189321000 Enhancers ES-UCSF4 Cell Line embryonic stem cell
12 chr4:189320200-189322000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
13 chr4:189320200-189322400 Enhancers Placenta Amnion Placenta Amnion
14 chr4:189320200-189322600 Enhancers HUES64 Cell Line embryonic stem cell
15 chr4:189320400-189320600 Weak transcription HUES6 Cell Line embryonic stem cell
16 chr4:189320400-189321600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived

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