Variant report

Variant rs569563140
Chromosome Location chr5:60297090-60297091
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:60266200-60317400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr5:60290200-60298400 Weak transcription Primary T helper 17 cells PMA-I stimulated --
3 chr5:60290200-60298400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
4 chr5:60292200-60297800 Weak transcription Pancreas Pancrea
5 chr5:60292200-60305800 Weak transcription Ovary ovary
6 chr5:60295000-60304200 Weak transcription HepG2 liver
7 chr5:60296000-60298400 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
8 chr5:60296400-60297200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr5:60296400-60297200 Enhancers Aorta Aorta
10 chr5:60296400-60297200 Enhancers Colon Smooth Muscle Colon
11 chr5:60296400-60298000 Enhancers Skeletal Muscle Female skeletal muscle
12 chr5:60296600-60300000 Enhancers Fetal Brain Female brain
13 chr5:60296800-60297200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
14 chr5:60297000-60297200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
15 chr5:60297000-60297400 Weak transcription Fetal Brain Male brain
16 chr5:60297000-60299800 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell

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