Variant report

Variant rs6932887
Chromosome Location chr6:53612089-53612090
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 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 chr6:53601800-53613400 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
3 chr6:53602200-53614800 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
4 chr6:53606400-53619600 Weak transcription Right Atrium heart
5 chr6:53609000-53612200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr6:53610200-53614000 Weak transcription Placenta Amnion Placenta Amnion
7 chr6:53610600-53612200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr6:53610600-53612200 Enhancers HMEC breast
9 chr6:53611600-53612200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr6:53611600-53612200 Enhancers Placenta Placenta
11 chr6:53611800-53612200 Enhancers NHEK skin
12 chr6:53612000-53614800 Weak transcription Hela-S3 cervix

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