Variant report

Variant rs57238821
Chromosome Location chr14:56248041-56248042
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:56238800-56251800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
2 chr14:56238800-56256600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
3 chr14:56246000-56248800 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr14:56246200-56248400 Enhancers HUVEC blood vessel
5 chr14:56246600-56248200 Enhancers Fetal Heart heart
6 chr14:56246600-56248200 Enhancers Stomach Mucosa stomach
7 chr14:56246600-56248600 Enhancers Lung lung
8 chr14:56246800-56248400 Enhancers NH-A brain
9 chr14:56246800-56248800 Enhancers Gastric stomach
10 chr14:56247000-56248400 Enhancers Pancreas Pancrea
11 chr14:56247000-56249000 Enhancers K562 blood
12 chr14:56247000-56249600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
13 chr14:56247400-56258400 Weak transcription Psoas Muscle Psoas
14 chr14:56247800-56248400 Enhancers Primary hematopoietic stem cells short term culture blood
15 chr14:56247800-56249200 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
16 chr14:56247800-56249400 Enhancers Hela-S3 cervix
17 chr14:56247800-56256800 Weak transcription Left Ventricle heart
18 chr14:56247800-56257400 Weak transcription Right Ventricle heart
19 chr14:56248000-56248200 Bivalent Enhancer Osteobl bone
20 chr14:56248000-56249000 Weak transcription Muscle Satellite Cultured Cells --

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