Variant report

Variant rs13208062
Chromosome Location chr6:15946845-15946846
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:15936400-15951200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr6:15944400-15951000 Weak transcription Gastric stomach
3 chr6:15945400-15947400 Enhancers Placenta Placenta
4 chr6:15945800-15947200 Enhancers Psoas Muscle Psoas
5 chr6:15945800-15948000 Enhancers Fetal Muscle Leg muscle
6 chr6:15946400-15949200 Weak transcription NH-A brain
7 chr6:15946400-15949400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
8 chr6:15946600-15949000 Weak transcription K562 blood
9 chr6:15946600-15949200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr6:15946600-15949200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr6:15946600-15949200 Weak transcription HUVEC blood vessel
12 chr6:15946600-15949400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr6:15946800-15949400 Weak transcription NHEK skin

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