Variant report

Variant rs34944646
Chromosome Location chr1:153343941-153343942
allele -/A
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:153333600-153346200 Enhancers Primary monocytes fromperipheralblood blood
2 chr1:153340000-153350400 Enhancers Fetal Intestine Large intestine
3 chr1:153340400-153344000 Enhancers Fetal Intestine Small intestine
4 chr1:153340400-153349000 Weak transcription Spleen Spleen
5 chr1:153341400-153347800 Weak transcription Placenta Placenta
6 chr1:153342600-153346200 Weak transcription Esophagus oesophagus
7 chr1:153343200-153344600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr1:153343200-153344600 Enhancers HMEC breast
9 chr1:153343200-153344600 Enhancers NHEK skin
10 chr1:153343200-153344800 Flanking Active TSS Monocytes-CD14+_RO01746 blood
11 chr1:153343200-153345800 Flanking Active TSS Primary neutrophils fromperipheralblood blood
12 chr1:153343200-153347400 Weak transcription Fetal Adrenal Gland Adrenal Gland
13 chr1:153343400-153344400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
14 chr1:153343600-153344400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin

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