Variant report

Variant rs9371794
Chromosome Location chr6:150493191-150493192
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:150474200-150493600 Weak transcription Right Ventricle heart
2 chr6:150479200-150495800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr6:150486200-150497400 Weak transcription Right Atrium heart
4 chr6:150488200-150497800 Weak transcription Colonic Mucosa Colon
5 chr6:150490600-150494200 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
6 chr6:150491400-150497200 Weak transcription NHEK skin
7 chr6:150491400-150497600 Weak transcription K562 blood
8 chr6:150491400-150506400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr6:150491600-150496600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr6:150491600-150496800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr6:150491600-150501400 Weak transcription HMEC breast
12 chr6:150492000-150494200 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
13 chr6:150492200-150495000 Enhancers Skeletal Muscle Female skeletal muscle
14 chr6:150492200-150496600 Enhancers Fetal Heart heart
15 chr6:150492400-150493600 Weak transcription Psoas Muscle Psoas
16 chr6:150492600-150493200 Enhancers Fetal Muscle Leg muscle
17 chr6:150492800-150494400 Enhancers Left Ventricle heart

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