Variant report

Variant rs2973764
Chromosome Location chr5:177706253-177706254
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:177702200-177706800 Weak transcription Fetal Heart heart
2 chr5:177703400-177706800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
3 chr5:177703600-177728800 Weak transcription Right Atrium heart
4 chr5:177705200-177706600 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
5 chr5:177705200-177706800 Weak transcription Spleen Spleen
6 chr5:177705800-177707800 Enhancers Primary hematopoietic stem cells short term culture blood
7 chr5:177706000-177706800 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr5:177706000-177707400 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
9 chr5:177706200-177706600 Bivalent Enhancer Placenta Placenta
10 chr5:177706200-177708000 Bivalent Enhancer Fetal Muscle Trunk muscle

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