Variant report

Variant rs17307291
Chromosome Location chr16:55698510-55698511
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr16:55692600-55705400 Enhancers Placenta Placenta
2 chr16:55693600-55699400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr16:55693600-55699400 Enhancers NHEK skin
4 chr16:55693800-55699000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr16:55695000-55699400 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
6 chr16:55695400-55699600 Enhancers HMEC breast
7 chr16:55695600-55703800 Enhancers Breast Myoepithelial Primary Cells Breast
8 chr16:55695800-55699400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr16:55696000-55699400 Enhancers Placenta Amnion Placenta Amnion
10 chr16:55697200-55700200 Enhancers HepG2 liver
11 chr16:55697400-55699000 Enhancers Adipose Nuclei Adipose
12 chr16:55697800-55699200 Enhancers Brain Hippocampus Middle brain
13 chr16:55698000-55700200 Enhancers Pancreas Pancrea
14 chr16:55698200-55698600 Enhancers Esophagus oesophagus
15 chr16:55698200-55700200 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
16 chr16:55698400-55698600 Enhancers Brain Angular Gyrus brain
17 chr16:55698400-55698600 Enhancers Brain Substantia Nigra brain
18 chr16:55698400-55698800 Bivalent Enhancer Fetal Muscle Trunk muscle
19 chr16:55698400-55702200 Weak transcription Fetal Muscle Leg muscle

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