Variant report

Variant rs57396814
Chromosome Location chr12:31175277-31175278
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:31147200-31185000 Weak transcription Right Atrium heart
2 chr12:31161600-31176400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr12:31162800-31176200 Weak transcription Fetal Brain Female brain
4 chr12:31168600-31177000 Enhancers Fetal Thymus thymus
5 chr12:31169000-31185000 Weak transcription Right Ventricle heart
6 chr12:31172000-31175600 Weak transcription Adipose Nuclei Adipose
7 chr12:31172600-31175600 Enhancers Thymus Thymus
8 chr12:31173200-31176000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
9 chr12:31173400-31176800 Enhancers HUVEC blood vessel
10 chr12:31174000-31180000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
11 chr12:31174800-31176800 Enhancers Fetal Adrenal Gland Adrenal Gland
12 chr12:31174800-31177000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
13 chr12:31175000-31175400 Enhancers A549 lung
14 chr12:31175000-31175600 Flanking Active TSS hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
15 chr12:31175000-31175800 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
16 chr12:31175200-31175400 Enhancers HepG2 liver
17 chr12:31175200-31175600 Weak transcription Spleen Spleen

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