Variant report

Variant rs71418693
Chromosome Location chr2:209360727-209360728
allele A/G/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:209355200-209361000 Weak transcription Stomach Mucosa stomach
2 chr2:209355200-209366000 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
3 chr2:209356600-209361000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
4 chr2:209360000-209361000 Enhancers HUES64 Cell Line embryonic stem cell
5 chr2:209360000-209361200 Enhancers iPS-20b Cell Line embryonic stem cell
6 chr2:209360200-209361200 Enhancers H1 Cell Line embryonic stem cell
7 chr2:209360200-209361200 Enhancers HUES6 Cell Line embryonic stem cell
8 chr2:209360200-209361400 Enhancers iPS-18 Cell Line embryonic stem cell
9 chr2:209360200-209361600 Enhancers HUES48 Cell Line embryonic stem cell
10 chr2:209360400-209361200 Enhancers iPS-15b Cell Line embryonic stem cell
11 chr2:209360600-209360800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell

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