Variant report

Variant rs3027066
Chromosome Location chr1:159188230-159188231
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:159158800-159188800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr1:159181400-159188400 Weak transcription iPS-15b Cell Line embryonic stem cell
3 chr1:159185000-159190400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
4 chr1:159186400-159188400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
5 chr1:159188000-159189200 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
6 chr1:159188000-159190400 Enhancers H1 Cell Line embryonic stem cell
7 chr1:159188200-159188400 Enhancers iPS-20b Cell Line embryonic stem cell
8 chr1:159188200-159188600 Enhancers iPS-18 Cell Line embryonic stem cell
9 chr1:159188200-159188600 Enhancers Fetal Brain Female brain
10 chr1:159188200-159189000 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
11 chr1:159188200-159189200 Enhancers Brain Germinal Matrix brain
12 chr1:159188200-159189400 Enhancers HUES6 Cell Line embryonic stem cell
13 chr1:159188200-159189400 Enhancers Fetal Brain Male brain
14 chr1:159188200-159190200 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
15 chr1:159188200-159190200 Enhancers ES-UCSF4 Cell Line embryonic stem cell

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