Variant report

Variant rs56024406
Chromosome Location chr2:171591642-171591643
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:171574000-171620800 Weak transcription Pancreas Pancrea
2 chr2:171586400-171592200 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
3 chr2:171591200-171594200 Weak transcription HMEC breast
4 chr2:171591400-171595000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr2:171591400-171595200 Weak transcription Fetal Intestine Large intestine
6 chr2:171591600-171593200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr2:171591600-171593800 Weak transcription NHEK skin
8 chr2:171591600-171594000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr2:171591600-171595200 Weak transcription Placenta Placenta

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