Variant report

Variant rs7537947
Chromosome Location chr1:225203656-225203657
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:225199400-225207000 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
2 chr1:225201200-225206200 ZNF genes & repeats Primary hematopoietic stem cells G-CSF-mobilized Male --
3 chr1:225202000-225205200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr1:225202200-225203800 ZNF genes & repeats Primary hematopoietic stem cells blood
5 chr1:225202200-225204800 Weak transcription Fetal Stomach stomach
6 chr1:225202800-225204000 Strong transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr1:225202800-225204800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr1:225203400-225203800 ZNF genes & repeats H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
9 chr1:225203400-225203800 ZNF genes & repeats H1 Derived Mesenchymal Stem Cells ES cell derived
10 chr1:225203400-225203800 ZNF genes & repeats Primary hematopoietic stem cells short term culture blood
11 chr1:225203400-225203800 ZNF genes & repeats Ovary ovary
12 chr1:225203400-225204000 ZNF genes & repeats Fetal Intestine Small intestine
13 chr1:225203400-225205000 Weak transcription Fetal Intestine Large intestine
14 chr1:225203600-225203800 ZNF genes & repeats Pancreas Pancrea

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