Variant report

Variant rs34880762
Chromosome Location chr6:53615733-53615734
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:53601600-53638000 Weak transcription Primary hematopoietic stem cells blood
2 chr6:53606400-53619600 Weak transcription Right Atrium heart
3 chr6:53612200-53616200 Weak transcription HMEC breast
4 chr6:53612200-53616600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr6:53612200-53616800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr6:53612200-53617400 Weak transcription Placenta Placenta
7 chr6:53614000-53617000 Enhancers Brain Germinal Matrix brain
8 chr6:53614000-53618200 Enhancers Placenta Amnion Placenta Amnion
9 chr6:53614400-53615800 Enhancers Fetal Brain Male brain
10 chr6:53614600-53615800 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
11 chr6:53614800-53615800 Enhancers Hela-S3 cervix
12 chr6:53614800-53618800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr6:53615200-53615800 Enhancers Fetal Adrenal Gland Adrenal Gland
14 chr6:53615600-53616600 Weak transcription NHEK skin

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