Variant report

Variant rs534129465
Chromosome Location chr15:76870856-76870857
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr15:76862600-76872000 Weak transcription Primary T helper memory cells from peripheral blood 2 blood
2 chr15:76868400-76871000 Enhancers Ovary ovary
3 chr15:76868800-76871000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr15:76868800-76871200 Enhancers NHEK skin
5 chr15:76869000-76871000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr15:76869400-76881200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr15:76870000-76871000 Strong transcription Fetal Intestine Small intestine
8 chr15:76870000-76871800 Weak transcription Fetal Intestine Large intestine
9 chr15:76870200-76872600 Weak transcription Brain Substantia Nigra brain
10 chr15:76870400-76872000 Weak transcription Spleen Spleen
11 chr15:76870400-76876000 Weak transcription Right Ventricle heart
12 chr15:76870400-76881200 Weak transcription Lung lung
13 chr15:76870800-76874000 Weak transcription Esophagus oesophagus

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