Variant report

Variant rs57339712
Chromosome Location chr21:46427399-46427400
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr21:46414600-46431800 Weak transcription Right Atrium heart
2 chr21:46421600-46429400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr21:46421800-46432200 Weak transcription Esophagus oesophagus
4 chr21:46426400-46427600 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
5 chr21:46426600-46427400 Enhancers Placenta Placenta
6 chr21:46426600-46427600 Flanking Active TSS Hela-S3 cervix
7 chr21:46426600-46428000 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
8 chr21:46426600-46428000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr21:46426600-46432000 Enhancers Breast Myoepithelial Primary Cells Breast
10 chr21:46426800-46427400 Active TSS Brain Anterior Caudate brain
11 chr21:46426800-46429600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr21:46427000-46428000 Enhancers NHEK skin
13 chr21:46427200-46428800 Bivalent Enhancer HepG2 liver

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