Variant report

Variant rs4772
Chromosome Location chr1:153346263-153346264
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:153340000-153350400 Enhancers Fetal Intestine Large intestine
2 chr1:153340400-153349000 Weak transcription Spleen Spleen
3 chr1:153341400-153347800 Weak transcription Placenta Placenta
4 chr1:153343200-153347400 Weak transcription Fetal Adrenal Gland Adrenal Gland
5 chr1:153344400-153346600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr1:153344400-153346800 Enhancers Fetal Intestine Small intestine
7 chr1:153344400-153347800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr1:153344600-153346400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr1:153344600-153346600 Weak transcription HMEC breast
10 chr1:153344600-153347800 Weak transcription NHEK skin
11 chr1:153345800-153346400 Transcr. at gene 5' and 3' Primary neutrophils fromperipheralblood blood
12 chr1:153345800-153346800 Active TSS Primary B cells from cord blood blood
13 chr1:153345800-153351800 Flanking Active TSS Monocytes-CD14+_RO01746 blood
14 chr1:153346200-153346400 Enhancers Esophagus oesophagus
15 chr1:153346200-153348200 Flanking Active TSS Primary monocytes fromperipheralblood blood

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