Variant report

Variant rs552547890
Chromosome Location chr1:103394203-103394204
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:103352600-103403200 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
2 chr1:103369600-103498600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
3 chr1:103378800-103400000 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr1:103380000-103399000 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
5 chr1:103381200-103399400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
6 chr1:103385800-103401000 Weak transcription HSMM muscle
7 chr1:103386000-103407000 Weak transcription NH-A brain
8 chr1:103386200-103399600 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
9 chr1:103386200-103482000 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
10 chr1:103387000-103394400 Strong transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
11 chr1:103393600-103399200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
12 chr1:103394200-103399000 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
13 chr1:103394200-103399000 Weak transcription Cortex derived primary cultured neurospheres brain
14 chr1:103394200-103399000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin

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