Variant report

Variant rs17568791
Chromosome Location chr2:51021488-51021489
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:51018000-51023200 Weak transcription Fetal Brain Male brain
2 chr2:51020600-51022800 Enhancers iPS-18 Cell Line embryonic stem cell
3 chr2:51020600-51023400 Enhancers HUES64 Cell Line embryonic stem cell
4 chr2:51020800-51021600 Enhancers H1 Cell Line embryonic stem cell
5 chr2:51020800-51022800 Enhancers HUES48 Cell Line embryonic stem cell
6 chr2:51020800-51023000 Enhancers iPS-15b Cell Line embryonic stem cell
7 chr2:51021000-51023200 Enhancers iPS-20b Cell Line embryonic stem cell
8 chr2:51021200-51021600 Enhancers ES-WA7 Cell Line embryonic stem cell
9 chr2:51021200-51021800 Weak transcription ES-I3 Cell Line embryonic stem cell
10 chr2:51021200-51021800 Enhancers HUES6 Cell Line embryonic stem cell
11 chr2:51021400-51022200 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
12 chr2:51021400-51023000 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived

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