Variant report

Variant rs4607907
Chromosome Location chr1:57930136-57930137
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:57917400-57933800 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
2 chr1:57927400-57930200 Weak transcription NHLF lung
3 chr1:57927400-57930600 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr1:57929200-57931000 Enhancers Fetal Brain Female brain
5 chr1:57929400-57931200 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
6 chr1:57929400-57931800 Enhancers HepG2 liver
7 chr1:57929800-57930200 Weak transcription Cortex derived primary cultured neurospheres brain
8 chr1:57930000-57931000 Enhancers Fetal Brain Male brain
9 chr1:57930000-57931000 Enhancers Pancreatic Islets Pancreatic Islet
10 chr1:57930000-57931000 Enhancers Hela-S3 cervix

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