Variant report

Variant rs553695427
Chromosome Location chr7:128706193-128706194
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:128695800-128706200 Weak transcription H9 Cell Line embryonic stem cell
2 chr7:128696200-128706400 Weak transcription Right Atrium heart
3 chr7:128696600-128706200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
4 chr7:128703200-128706800 Weak transcription iPS-20b Cell Line embryonic stem cell
5 chr7:128705200-128708600 Weak transcription Monocytes-CD14+_RO01746 blood
6 chr7:128705400-128706400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
7 chr7:128705600-128706600 Weak transcription Fetal Intestine Small intestine
8 chr7:128705600-128706800 Weak transcription GM12878-XiMat blood
9 chr7:128705800-128706200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
10 chr7:128705800-128706200 Weak transcription Fetal Intestine Large intestine
11 chr7:128706000-128707400 Enhancers Placenta Placenta
12 chr7:128706000-128708000 Flanking Active TSS K562 blood
13 chr7:128706000-128709600 Enhancers Fetal Adrenal Gland Adrenal Gland

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