Variant report

Variant rs17822220
Chromosome Location chr6:79200267-79200268
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:79195800-79202000 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
2 chr6:79197400-79201800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr6:79197600-79201800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr6:79197600-79202000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr6:79197800-79201800 Weak transcription HSMM muscle
6 chr6:79199600-79201600 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
7 chr6:79199600-79201800 Enhancers HUVEC blood vessel
8 chr6:79199600-79202000 Weak transcription NH-A brain
9 chr6:79199800-79200600 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
10 chr6:79200000-79201000 Weak transcription Muscle Satellite Cultured Cells --
11 chr6:79200000-79202000 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
12 chr6:79200000-79202000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
13 chr6:79200000-79202000 Weak transcription HMEC breast

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