Variant report

Variant rs1539421
Chromosome Location chr6:15946677-15946678
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 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 chr6:15945400-15946800 Enhancers NHEK skin
4 chr6:15945400-15947400 Enhancers Placenta Placenta
5 chr6:15945800-15947200 Enhancers Psoas Muscle Psoas
6 chr6:15945800-15948000 Enhancers Fetal Muscle Leg muscle
7 chr6:15946400-15949200 Weak transcription NH-A brain
8 chr6:15946400-15949400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
9 chr6:15946600-15946800 Enhancers Fetal Muscle Trunk muscle
10 chr6:15946600-15949000 Weak transcription K562 blood
11 chr6:15946600-15949200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
12 chr6:15946600-15949200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
13 chr6:15946600-15949200 Weak transcription HUVEC blood vessel
14 chr6:15946600-15949400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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