Variant report

Variant rs16932650
Chromosome Location chr11:16180275-16180276
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:16172400-16191400 Weak transcription Cortex derived primary cultured neurospheres brain
2 chr11:16172600-16191400 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
3 chr11:16174200-16191200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
4 chr11:16175000-16180800 Enhancers NHEK skin
5 chr11:16175200-16180600 Enhancers HMEC breast
6 chr11:16177600-16181000 Enhancers A549 lung
7 chr11:16177600-16187800 Weak transcription Fetal Intestine Small intestine
8 chr11:16178000-16185200 Weak transcription Fetal Intestine Large intestine
9 chr11:16178800-16180800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr11:16179800-16180600 Enhancers Muscle Satellite Cultured Cells --
11 chr11:16179800-16181800 Weak transcription Psoas Muscle Psoas
12 chr11:16180000-16180600 Enhancers Hela-S3 cervix

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