Variant report

Variant rs6433238
Chromosome Location chr2:171589253-171589254
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:7 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:171574000-171620800 Weak transcription Pancreas Pancrea
2 chr2:171580200-171589600 Weak transcription Fetal Intestine Small intestine
3 chr2:171580800-171590400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr2:171584800-171590600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr2:171586400-171592200 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
6 chr2:171586800-171590000 Weak transcription Fetal Intestine Large intestine
7 chr2:171586800-171590800 Weak transcription HMEC breast

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