Variant report

Variant rs16932634
Chromosome Location chr11:16175759-16175760
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:16170800-16175800 Weak transcription Muscle Satellite Cultured Cells --
2 chr11:16172400-16176000 Weak transcription Fetal Intestine Small intestine
3 chr11:16172400-16191400 Weak transcription Cortex derived primary cultured neurospheres brain
4 chr11:16172600-16191400 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
5 chr11:16174200-16191200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
6 chr11:16174600-16176800 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
7 chr11:16174800-16178400 Enhancers Stomach Mucosa stomach
8 chr11:16174800-16180000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr11:16175000-16177000 Enhancers Hela-S3 cervix
10 chr11:16175000-16178400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
11 chr11:16175000-16180800 Enhancers NHEK skin
12 chr11:16175200-16177400 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
13 chr11:16175200-16177800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr11:16175200-16180600 Enhancers HMEC breast
15 chr11:16175400-16175800 Weak transcription Psoas Muscle Psoas
16 chr11:16175400-16179000 Enhancers Pancreatic Islets Pancreatic Islet
17 chr11:16175600-16176000 Enhancers Fetal Intestine Large intestine
18 chr11:16175600-16176200 Flanking Active TSS HepG2 liver
19 chr11:16175600-16177600 Flanking Active TSS A549 lung

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