Variant report

Variant rs6823718
Chromosome Location chr4:99063202-99063203
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:99056400-99063800 Weak transcription Primary T killer naive cells fromperipheralblood blood
2 chr4:99062400-99063600 Weak transcription Fetal Intestine Small intestine
3 chr4:99063000-99063400 Enhancers Pancreatic Islets Pancreatic Islet
4 chr4:99063000-99063600 Enhancers HUES48 Cell Line embryonic stem cell
5 chr4:99063000-99063600 Enhancers NHEK skin
6 chr4:99063200-99063400 Enhancers HMEC breast
7 chr4:99063200-99063600 Enhancers iPS-18 Cell Line embryonic stem cell
8 chr4:99063200-99063600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr4:99063200-99063600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr4:99063200-99063800 Enhancers iPS-15b Cell Line embryonic stem cell
11 chr4:99063200-99063800 Enhancers Primary T helper memory cells from peripheral blood 2 blood

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