Variant report

Variant rs3934352
Chromosome Location chr1:103492900-103492901
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:103369600-103498600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
2 chr1:103446800-103497800 Weak transcription HSMM muscle
3 chr1:103449200-103545200 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
4 chr1:103460200-103516400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
5 chr1:103475800-103516600 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
6 chr1:103487600-103493600 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
7 chr1:103489200-103516400 Weak transcription Cortex derived primary cultured neurospheres brain
8 chr1:103489600-103506000 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
9 chr1:103491600-103503800 Weak transcription NH-A brain
10 chr1:103492000-103496400 Weak transcription HUES64 Cell Line embryonic stem cell
11 chr1:103492200-103493000 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
12 chr1:103492400-103497200 Strong transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
13 chr1:103492600-103493800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin

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