Variant report

Variant rs13377722
Chromosome Location chr12:31176335-31176336
allele A/G
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 chr12:31168600-31177000 Enhancers Fetal Thymus thymus
4 chr12:31169000-31185000 Weak transcription Right Ventricle heart
5 chr12:31173400-31176800 Enhancers HUVEC blood vessel
6 chr12:31174000-31180000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
7 chr12:31174800-31176800 Enhancers Fetal Adrenal Gland Adrenal Gland
8 chr12:31174800-31177000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
9 chr12:31175600-31176600 Enhancers Adipose Nuclei Adipose
10 chr12:31175600-31176600 Enhancers Spleen Spleen
11 chr12:31176000-31176800 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
12 chr12:31176200-31176400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
13 chr12:31176200-31176400 Enhancers Fetal Muscle Leg muscle
14 chr12:31176200-31176800 Enhancers Thymus Thymus
15 chr12:31176200-31177400 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived

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