Variant report

Variant rs16937469
Chromosome Location chr8:49409457-49409458
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:49407000-49413800 Weak transcription NH-A brain
2 chr8:49407200-49413400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
3 chr8:49407200-49413400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr8:49407200-49413400 Weak transcription A549 lung
5 chr8:49407400-49413400 Weak transcription Osteobl bone
6 chr8:49409000-49409800 Enhancers ES-UCSF4 Cell Line embryonic stem cell
7 chr8:49409200-49409800 Enhancers ES-I3 Cell Line embryonic stem cell
8 chr8:49409200-49409800 Enhancers iPS-18 Cell Line embryonic stem cell
9 chr8:49409200-49413400 Weak transcription Esophagus oesophagus
10 chr8:49409400-49409800 Enhancers ES-WA7 Cell Line embryonic stem cell
11 chr8:49409400-49409800 Enhancers H9 Cell Line embryonic stem cell
12 chr8:49409400-49409800 Enhancers HUES6 Cell Line embryonic stem cell
13 chr8:49409400-49409800 Enhancers iPS-20b Cell Line embryonic stem cell

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