Variant report

Variant rs35963574
Chromosome Location chr1:217314861-217314862
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:217314000-217315200 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
2 chr1:217314200-217318200 Weak transcription Aorta Aorta
3 chr1:217314400-217315200 Bivalent Enhancer ES-I3 Cell Line embryonic stem cell
4 chr1:217314400-217315200 Bivalent Enhancer H9 Cell Line embryonic stem cell
5 chr1:217314400-217315800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
6 chr1:217314400-217316000 Bivalent Enhancer iPS-18 Cell Line embryonic stem cell
7 chr1:217314600-217315200 Bivalent Enhancer iPS-20b Cell Line embryonic stem cell
8 chr1:217314600-217315400 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
9 chr1:217314600-217315400 Bivalent Enhancer HUES48 Cell Line embryonic stem cell
10 chr1:217314600-217315400 Bivalent Enhancer HUES64 Cell Line embryonic stem cell
11 chr1:217314600-217315400 Bivalent Enhancer iPS-15b Cell Line embryonic stem cell
12 chr1:217314600-217316200 Enhancers Fetal Heart heart

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