Variant report

Variant rs17797565
Chromosome Location chr4:56797521-56797522
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:56774000-56803200 Weak transcription HUVEC blood vessel
2 chr4:56792800-56798400 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
3 chr4:56793200-56799800 Weak transcription Primary B cells from peripheral blood blood
4 chr4:56793400-56804400 Weak transcription Sigmoid Colon Sigmoid Colon
5 chr4:56794600-56797800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr4:56794800-56798200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
7 chr4:56796400-56797600 Enhancers Primary hematopoietic stem cells short term culture blood
8 chr4:56796400-56797800 Weak transcription Fetal Intestine Large intestine
9 chr4:56796600-56798000 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
10 chr4:56796600-56798400 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
11 chr4:56796800-56797600 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
12 chr4:56796800-56798200 Enhancers Primary hematopoietic stem cells blood
13 chr4:56797000-56797800 Flanking Active TSS Primary hematopoietic stem cells G-CSF-mobilized Male --
14 chr4:56797000-56799200 Enhancers Placenta Amnion Placenta Amnion
15 chr4:56797200-56798800 Enhancers NHDF-Ad bronchial
16 chr4:56797400-56798800 Enhancers HSMM muscle
17 chr4:56797400-56799400 Weak transcription Fetal Intestine Small intestine

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