Variant report

Variant rs534859425
Chromosome Location chr2:132977814-132977815
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:132976800-132996200 Weak transcription NHEK skin
2 chr2:132977200-132980600 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
3 chr2:132977400-132980600 Weak transcription K562 blood
4 chr2:132977800-132980200 Weak transcription Adipose Nuclei Adipose
5 chr2:132977800-132980400 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
6 chr2:132977800-132980400 Weak transcription HUES48 Cell Line embryonic stem cell
7 chr2:132977800-132980400 Weak transcription HUES64 Cell Line embryonic stem cell
8 chr2:132977800-132980400 Weak transcription iPS-20b Cell Line embryonic stem cell
9 chr2:132977800-132980600 Weak transcription iPS-18 Cell Line embryonic stem cell
10 chr2:132977800-132980600 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr2:132977800-132980600 Weak transcription Primary T cells from cord blood blood
12 chr2:132977800-132980600 Weak transcription Fetal Brain Male brain
13 chr2:132977800-132980600 Weak transcription Fetal Heart heart
14 chr2:132977800-132980600 Weak transcription Pancreatic Islets Pancreatic Islet
15 chr2:132977800-132980600 Weak transcription HUVEC blood vessel
16 chr2:132977800-132980600 Weak transcription Osteobl bone

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