Variant report

Variant rs9479997
Chromosome Location chr6:150553989-150553990
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:150549800-150554000 Weak transcription Psoas Muscle Psoas
2 chr6:150549800-150556400 Weak transcription Left Ventricle heart
3 chr6:150550000-150556600 Weak transcription Skeletal Muscle Female skeletal muscle
4 chr6:150550000-150558600 Weak transcription Skeletal Muscle Male skeletal muscle
5 chr6:150550800-150554800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr6:150550800-150555400 Enhancers HMEC breast
7 chr6:150551000-150555000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr6:150551200-150558800 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
9 chr6:150551600-150554000 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
10 chr6:150552400-150554200 Weak transcription Right Ventricle heart
11 chr6:150552400-150557600 Weak transcription Right Atrium heart
12 chr6:150552400-150558600 Weak transcription Fetal Brain Female brain
13 chr6:150552600-150555000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
14 chr6:150552600-150557400 Weak transcription Fetal Lung lung
15 chr6:150552600-150559400 Weak transcription Lung lung
16 chr6:150552800-150555400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
17 chr6:150553000-150556400 Weak transcription Fetal Heart heart
18 chr6:150553000-150557400 Weak transcription Fetal Brain Male brain
19 chr6:150553400-150554400 Flanking Active TSS NHEK skin
20 chr6:150553600-150554000 Active TSS Osteobl bone

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