Variant report

Variant rs6904292
Chromosome Location chr6:78001615-78001616
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:77999000-78005400 Enhancers HUVEC blood vessel
2 chr6:77999800-78002000 Enhancers NHEK skin
3 chr6:78000000-78002800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
4 chr6:78000000-78003800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
5 chr6:78000200-78002400 Enhancers HMEC breast
6 chr6:78000600-78001800 Weak transcription NHDF-Ad bronchial
7 chr6:78000800-78001800 Weak transcription Breast Myoepithelial Primary Cells Breast
8 chr6:78000800-78001800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr6:78000800-78001800 Active TSS Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr6:78000800-78002200 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
11 chr6:78001000-78002000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
12 chr6:78001400-78002200 Enhancers HSMM muscle
13 chr6:78001400-78002800 Enhancers Muscle Satellite Cultured Cells --
14 chr6:78001400-78003800 Enhancers Osteobl bone
15 chr6:78001600-78002400 Enhancers Placenta Amnion Placenta Amnion
16 chr6:78001600-78002800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
17 chr6:78001600-78004000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow

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