Variant report

Variant rs551896297
Chromosome Location chr12:50348537-50348538
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:50339400-50353600 Weak transcription Right Atrium heart
2 chr12:50347000-50348800 Bivalent Enhancer Fetal Muscle Leg muscle
3 chr12:50347400-50353400 Weak transcription Pancreas Pancrea
4 chr12:50347600-50348800 Enhancers Hela-S3 cervix
5 chr12:50347600-50349000 Weak transcription Spleen Spleen
6 chr12:50347600-50349400 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin01 Skin
7 chr12:50347800-50348600 Bivalent Enhancer iPS DF 19.11 Cell Line embryonic stem cell
8 chr12:50347800-50349800 Enhancers ES-UCSF4 Cell Line embryonic stem cell
9 chr12:50348400-50348600 Bivalent Enhancer HUES6 Cell Line embryonic stem cell
10 chr12:50348400-50348800 Bivalent Enhancer H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
11 chr12:50348400-50348800 Bivalent Enhancer hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
12 chr12:50348400-50348800 Bivalent Enhancer Fetal Adrenal Gland Adrenal Gland
13 chr12:50348400-50349000 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin03 Skin
14 chr12:50348400-50349600 Bivalent Enhancer Primary hematopoietic stem cells G-CSF-mobilized Male --
15 chr12:50348400-50350800 Bivalent Enhancer Primary hematopoietic stem cells G-CSF-mobilized Female --

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