Variant report

Variant rs7144635
Chromosome Location chr14:67111882-67111883
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:67095400-67116600 Weak transcription Brain Substantia Nigra brain
2 chr14:67095800-67112000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr14:67101400-67119600 Weak transcription Aorta Aorta
4 chr14:67102000-67119400 Weak transcription Pancreas Pancrea
5 chr14:67106000-67112000 Weak transcription Osteobl bone
6 chr14:67109200-67118400 Weak transcription Psoas Muscle Psoas
7 chr14:67109800-67113600 Enhancers HUVEC blood vessel
8 chr14:67110600-67112000 Weak transcription HMEC breast
9 chr14:67110800-67112000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
10 chr14:67110800-67116600 Weak transcription HSMM muscle
11 chr14:67110800-67117000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
12 chr14:67111000-67112000 Weak transcription NHEK skin
13 chr14:67111200-67112000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr14:67111400-67117000 Weak transcription Pancreatic Islets Pancreatic Islet
15 chr14:67111400-67119200 Weak transcription Skeletal Muscle Male skeletal muscle
16 chr14:67111400-67119400 Weak transcription iPS-20b Cell Line embryonic stem cell
17 chr14:67111600-67117400 Weak transcription HUES64 Cell Line embryonic stem cell
18 chr14:67111600-67118200 Weak transcription HUES48 Cell Line embryonic stem cell

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