Variant report

Variant rs13433547
Chromosome Location chr22:21260998-21260999
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr22:21240200-21270600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr22:21240200-21271000 Weak transcription Right Atrium heart
3 chr22:21254800-21263600 Weak transcription Primary hematopoietic stem cells short term culture blood
4 chr22:21258200-21261400 Enhancers HMEC breast
5 chr22:21258400-21261400 Enhancers Muscle Satellite Cultured Cells --
6 chr22:21258800-21271000 Weak transcription Esophagus oesophagus
7 chr22:21259600-21261000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr22:21259600-21261200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr22:21260200-21263400 Weak transcription Primary monocytes fromperipheralblood blood
10 chr22:21260200-21263600 Weak transcription Monocytes-CD14+_RO01746 blood
11 chr22:21260800-21263400 Weak transcription Primary neutrophils fromperipheralblood blood
12 chr22:21260800-21265200 Weak transcription NHEK skin
13 chr22:21260800-21265400 Weak transcription Hela-S3 cervix

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