Variant report

Variant rs61161120
Chromosome Location chr6:15947765-15947766
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 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 chr6:15945800-15948000 Enhancers Fetal Muscle Leg muscle
4 chr6:15946400-15949200 Weak transcription NH-A brain
5 chr6:15946400-15949400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
6 chr6:15946600-15949000 Weak transcription K562 blood
7 chr6:15946600-15949200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr6:15946600-15949200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr6:15946600-15949200 Weak transcription HUVEC blood vessel
10 chr6:15946600-15949400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr6:15946800-15949400 Weak transcription NHEK skin
12 chr6:15947000-15948000 Enhancers Skeletal Muscle Male skeletal muscle
13 chr6:15947200-15949600 Weak transcription Psoas Muscle Psoas
14 chr6:15947200-15952600 Weak transcription Right Atrium heart
15 chr6:15947400-15949600 Weak transcription Placenta Placenta

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