Variant report

Variant rs1923025
Chromosome Location chr1:120138083-120138084
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:120115200-120160800 Weak transcription Gastric stomach
2 chr1:120130200-120138800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
3 chr1:120130200-120139000 Weak transcription Left Ventricle heart
4 chr1:120133600-120144800 Weak transcription Placenta Placenta
5 chr1:120135200-120151000 Weak transcription Fetal Stomach stomach
6 chr1:120136400-120139200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr1:120136400-120139600 Enhancers HMEC breast
8 chr1:120136800-120139200 Enhancers Breast Myoepithelial Primary Cells Breast
9 chr1:120136800-120142800 Weak transcription Fetal Intestine Small intestine
10 chr1:120137200-120139400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
11 chr1:120137600-120139000 Enhancers NHEK skin
12 chr1:120137800-120138400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
13 chr1:120137800-120138400 Enhancers Brain Hippocampus Middle brain
14 chr1:120137800-120138800 Enhancers Brain Cingulate Gyrus brain
15 chr1:120138000-120138200 Enhancers Brain Dorsolateral Prefrontal Cortex brain
16 chr1:120138000-120138400 Enhancers Brain Angular Gyrus brain
17 chr1:120138000-120138800 Enhancers Brain Inferior Temporal Lobe brain

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