Variant report

Variant rs4605683
Chromosome Location chr4:76979327-76979328
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:76976000-76979800 Weak transcription Fetal Intestine Small intestine
2 chr4:76976000-76980800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
3 chr4:76976200-76979800 Weak transcription Fetal Intestine Large intestine
4 chr4:76976200-76980000 Weak transcription Primary monocytes fromperipheralblood blood
5 chr4:76976400-76980200 Weak transcription Rectal Mucosa Donor 31 rectum
6 chr4:76976600-76979400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr4:76976600-76979400 Weak transcription Stomach Mucosa stomach
8 chr4:76976600-76980600 Weak transcription Primary B cells from cord blood blood
9 chr4:76977000-76979400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr4:76977200-76979400 Weak transcription NHEK skin
11 chr4:76977200-76980000 Weak transcription K562 blood
12 chr4:76977400-76981600 Weak transcription Primary B cells from peripheral blood blood
13 chr4:76978000-76982800 Weak transcription HUES48 Cell Line embryonic stem cell
14 chr4:76978800-76979400 Enhancers GM12878-XiMat blood
15 chr4:76979200-76980600 Enhancers HMEC breast

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