Variant report

Variant rs929882
Chromosome Location chr16:74873913-74873914
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr16:74864800-74877200 Weak transcription Fetal Intestine Small intestine
2 chr16:74870600-74877000 Weak transcription Esophagus oesophagus
3 chr16:74871400-74876000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr16:74871600-74875800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr16:74871600-74875800 Weak transcription NHEK skin
6 chr16:74871600-74876000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr16:74871600-74876000 Weak transcription HMEC breast
8 chr16:74872600-74877000 Weak transcription Breast Myoepithelial Primary Cells Breast
9 chr16:74872800-74877600 Weak transcription ES-I3 Cell Line embryonic stem cell
10 chr16:74873400-74875200 Weak transcription Placenta Placenta

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