Variant report

Variant rs552417357
Chromosome Location chr1:76692476-76692477
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:76687400-76695000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
2 chr1:76689000-76693800 Enhancers Primary neutrophils fromperipheralblood blood
3 chr1:76690000-76694800 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
4 chr1:76692000-76694400 Weak transcription HUVEC blood vessel
5 chr1:76692200-76693000 Enhancers H1 Cell Line embryonic stem cell
6 chr1:76692200-76693000 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
7 chr1:76692200-76693800 Enhancers ES-UCSF4 Cell Line embryonic stem cell
8 chr1:76692200-76696000 Enhancers Fetal Thymus thymus
9 chr1:76692400-76693000 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
10 chr1:76692400-76695600 Enhancers H9 Cell Line embryonic stem cell
11 chr1:76692400-76698200 Enhancers iPS-18 Cell Line embryonic stem cell

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