Variant report

Variant rs35036
Chromosome Location chr12:31175617-31175618
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 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 chr12:31173200-31176000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
7 chr12:31173400-31176800 Enhancers HUVEC blood vessel
8 chr12:31174000-31180000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
9 chr12:31174800-31176800 Enhancers Fetal Adrenal Gland Adrenal Gland
10 chr12:31174800-31177000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
11 chr12:31175000-31175800 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
12 chr12:31175600-31176200 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
13 chr12:31175600-31176200 Weak transcription Thymus Thymus
14 chr12:31175600-31176600 Enhancers Adipose Nuclei Adipose
15 chr12:31175600-31176600 Enhancers Spleen Spleen

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