Variant report

Variant rs56779238
Chromosome Location chr1:47675803-47675804
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:47664600-47676000 Weak transcription K562 blood
2 chr1:47673400-47677600 Enhancers HMEC breast
3 chr1:47673600-47676600 Bivalent Enhancer ES-UCSF4 Cell Line embryonic stem cell
4 chr1:47673800-47676000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
5 chr1:47674400-47677200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
6 chr1:47674400-47690600 Weak transcription Gastric stomach
7 chr1:47674600-47676000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
8 chr1:47675000-47677200 Weak transcription Spleen Spleen
9 chr1:47675200-47676200 Weak transcription Lung lung
10 chr1:47675200-47676800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr1:47675400-47676400 Weak transcription Right Atrium heart
12 chr1:47675400-47677000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr1:47675400-47680000 Enhancers HUVEC blood vessel
14 chr1:47675600-47676000 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin02 Skin
15 chr1:47675600-47676400 Bivalent Enhancer iPS DF 19.11 Cell Line embryonic stem cell
16 chr1:47675600-47676400 Enhancers NHEK skin
17 chr1:47675600-47677400 Bivalent Enhancer Fetal Adrenal Gland Adrenal Gland
18 chr1:47675800-47676200 Bivalent Enhancer H1 Cell Line embryonic stem cell
19 chr1:47675800-47677400 Enhancers Primary hematopoietic stem cells short term culture blood
20 chr1:47675800-47680600 Enhancers Primary hematopoietic stem cells blood

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