Variant report

Variant rs12749361
Chromosome Location chr1:103489190-103489191
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 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 chr1:103453400-103490000 Weak transcription NH-A brain
5 chr1:103460200-103516400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
6 chr1:103475800-103516600 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
7 chr1:103486600-103489200 Strong transcription Cortex derived primary cultured neurospheres brain
8 chr1:103486600-103491800 Strong transcription Foreskin Melanocyte Primary Cells skin03 Skin
9 chr1:103486800-103489600 Strong transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
10 chr1:103486800-103491200 Strong transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
11 chr1:103487000-103491600 Strong transcription HUES64 Cell Line embryonic stem cell
12 chr1:103487000-103492200 Strong transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
13 chr1:103487600-103493600 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
14 chr1:103488000-103490800 Weak transcription Brain Germinal Matrix brain

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