Variant report

Variant rs4668306
Chromosome Location chr2:171590018-171590019
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:171574000-171620800 Weak transcription Pancreas Pancrea
2 chr2:171580800-171590400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr2:171584800-171590600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr2:171586400-171592200 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
5 chr2:171586800-171590800 Weak transcription HMEC breast
6 chr2:171590000-171590200 Active TSS Fetal Intestine Large intestine
7 chr2:171590000-171590400 Flanking Active TSS Fetal Intestine Small intestine
8 chr2:171590000-171591600 Enhancers NHEK skin

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