Variant report

Variant rs16970734
Chromosome Location chr15:40771097-40771098
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr15:40764600-40771400 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
2 chr15:40765000-40772400 Weak transcription Esophagus oesophagus
3 chr15:40765000-40773400 Weak transcription Cortex derived primary cultured neurospheres brain
4 chr15:40767600-40771400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
5 chr15:40769800-40771200 Enhancers K562 blood
6 chr15:40770400-40771200 Enhancers Hela-S3 cervix
7 chr15:40770800-40774400 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
8 chr15:40771000-40771400 Enhancers HUES6 Cell Line embryonic stem cell
9 chr15:40771000-40771600 Bivalent/Poised TSS Foreskin Fibroblast Primary Cells skin02 Skin

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