Variant report

Variant rs12561917
Chromosome Location chr1:159189935-159189936
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:159185000-159190400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
2 chr1:159188000-159190400 Enhancers H1 Cell Line embryonic stem cell
3 chr1:159188200-159190200 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
4 chr1:159188200-159190200 Enhancers ES-UCSF4 Cell Line embryonic stem cell
5 chr1:159188400-159191000 Enhancers HUES64 Cell Line embryonic stem cell
6 chr1:159188600-159190200 Enhancers ES-I3 Cell Line embryonic stem cell
7 chr1:159189000-159190800 Enhancers Fetal Brain Female brain
8 chr1:159189200-159191000 Enhancers HUES48 Cell Line embryonic stem cell
9 chr1:159189400-159190600 Weak transcription HUES6 Cell Line embryonic stem cell
10 chr1:159189600-159190600 Weak transcription iPS-20b Cell Line embryonic stem cell
11 chr1:159189600-159190800 Weak transcription iPS-15b Cell Line embryonic stem cell
12 chr1:159189600-159190800 Enhancers iPS-18 Cell Line embryonic stem cell

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