Variant report

Variant rs376291380
Chromosome Location chr10:1644903-1644904
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:1634600-1648200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr10:1643000-1645000 Bivalent Enhancer Fetal Lung lung
3 chr10:1643200-1645200 Weak transcription Esophagus oesophagus
4 chr10:1644600-1648600 Weak transcription Fetal Thymus thymus
5 chr10:1644800-1645000 Genic enhancers H9 Cell Line embryonic stem cell
6 chr10:1644800-1645000 Active TSS Fetal Brain Male brain
7 chr10:1644800-1645200 Bivalent/Poised TSS Fetal Kidney kidney
8 chr10:1644800-1645200 Active TSS NHDF-Ad bronchial

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