Variant report

Variant rs3006475
Chromosome Location chr1:153344636-153344637
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 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 chr1:153340400-153349000 Weak transcription Spleen Spleen
4 chr1:153341400-153347800 Weak transcription Placenta Placenta
5 chr1:153342600-153346200 Weak transcription Esophagus oesophagus
6 chr1:153343200-153344800 Flanking Active TSS Monocytes-CD14+_RO01746 blood
7 chr1:153343200-153345800 Flanking Active TSS Primary neutrophils fromperipheralblood blood
8 chr1:153343200-153347400 Weak transcription Fetal Adrenal Gland Adrenal Gland
9 chr1:153344400-153345600 Enhancers Primary B cells from cord blood blood
10 chr1:153344400-153346600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr1:153344400-153346800 Enhancers Fetal Intestine Small intestine
12 chr1:153344400-153347800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
13 chr1:153344600-153344800 Enhancers Primary hematopoietic stem cells blood
14 chr1:153344600-153346400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
15 chr1:153344600-153346600 Weak transcription HMEC breast
16 chr1:153344600-153347800 Weak transcription NHEK skin

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