Variant report

Variant rs12588348
Chromosome Location chr14:37720439-37720440
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:37694800-37756400 Weak transcription Aorta Aorta
2 chr14:37706400-37723200 Weak transcription NHEK skin
3 chr14:37710400-37724000 Weak transcription iPS-18 Cell Line embryonic stem cell
4 chr14:37710600-37722000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
5 chr14:37710600-37723800 Weak transcription HUES48 Cell Line embryonic stem cell
6 chr14:37710800-37721200 Weak transcription H1 Cell Line embryonic stem cell
7 chr14:37715800-37722600 Enhancers Liver Liver
8 chr14:37716000-37729400 Weak transcription Psoas Muscle Psoas
9 chr14:37716000-37732800 Weak transcription Fetal Lung lung
10 chr14:37716000-37770600 Weak transcription A549 lung
11 chr14:37717600-37723200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr14:37717600-37726400 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
13 chr14:37717800-37721600 Weak transcription HUVEC blood vessel
14 chr14:37717800-37738600 Weak transcription Fetal Intestine Small intestine
15 chr14:37718000-37737600 Weak transcription Breast Myoepithelial Primary Cells Breast
16 chr14:37718200-37723800 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
17 chr14:37719600-37721600 Weak transcription HepG2 liver

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