Variant report

Variant rs9927096
Chromosome Location chr16:47896642-47896643
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr16:47883400-47899600 Weak transcription H9 Cell Line embryonic stem cell
2 chr16:47893200-47899200 Weak transcription Fetal Adrenal Gland Adrenal Gland
3 chr16:47893400-47899200 Weak transcription NHEK skin
4 chr16:47893600-47897200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
5 chr16:47893600-47897800 Weak transcription HUES6 Cell Line embryonic stem cell
6 chr16:47893800-47899400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr16:47893800-47899600 Weak transcription Fetal Brain Male brain
8 chr16:47894400-47900000 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
9 chr16:47895000-47897800 Weak transcription A549 lung
10 chr16:47895000-47899800 Weak transcription Pancreas Pancrea
11 chr16:47895000-47899800 Weak transcription Spleen Spleen
12 chr16:47896200-47899800 Weak transcription Lung lung

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