Variant report

Variant rs28660699
Chromosome Location chr4:22370739-22370740
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:22329000-22389400 Weak transcription Pancreas Pancrea
2 chr4:22336600-22385400 Weak transcription Fetal Intestine Large intestine
3 chr4:22354000-22378200 Weak transcription Aorta Aorta
4 chr4:22365600-22386800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr4:22365800-22384600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr4:22366000-22371400 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
7 chr4:22366000-22385000 Weak transcription NHEK skin
8 chr4:22368800-22418600 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived

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