Variant report

Variant rs61079197
Chromosome Location chr6:150560313-150560314
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:150555200-150561400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr6:150556600-150560400 Enhancers Skeletal Muscle Female skeletal muscle
3 chr6:150557000-150560400 Strong transcription Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr6:150557600-150568800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr6:150558800-150560400 Enhancers Fetal Brain Male brain
6 chr6:150559000-150560400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
7 chr6:150559400-150560600 Bivalent Enhancer Primary monocytes fromperipheralblood blood
8 chr6:150559600-150560400 Bivalent Enhancer Monocytes-CD14+_RO01746 blood
9 chr6:150559800-150565000 Weak transcription NHEK skin
10 chr6:150559800-150565000 Weak transcription Osteobl bone
11 chr6:150559800-150565400 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
12 chr6:150559800-150568800 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
13 chr6:150560000-150560400 Genic enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr6:150560000-150562200 Weak transcription Psoas Muscle Psoas
15 chr6:150560000-150563400 Weak transcription Fetal Heart heart
16 chr6:150560000-150565400 Weak transcription K562 blood
17 chr6:150560200-150568400 Weak transcription Duodenum Mucosa Duodenum
18 chr6:150560200-150571000 Weak transcription HMEC breast

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