Variant report

Variant rs55689121
Chromosome Location chr11:16175385-16175386
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:16170800-16175800 Weak transcription Muscle Satellite Cultured Cells --
2 chr11:16171600-16175600 Weak transcription Fetal Intestine Large intestine
3 chr11:16172400-16176000 Weak transcription Fetal Intestine Small intestine
4 chr11:16172400-16191400 Weak transcription Cortex derived primary cultured neurospheres brain
5 chr11:16172600-16191400 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
6 chr11:16173400-16175600 Enhancers HepG2 liver
7 chr11:16173800-16175400 Weak transcription Pancreatic Islets Pancreatic Islet
8 chr11:16174200-16191200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
9 chr11:16174600-16176800 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
10 chr11:16174800-16175600 Enhancers A549 lung
11 chr11:16174800-16178400 Enhancers Stomach Mucosa stomach
12 chr11:16174800-16180000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
13 chr11:16175000-16177000 Enhancers Hela-S3 cervix
14 chr11:16175000-16178400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
15 chr11:16175000-16180800 Enhancers NHEK skin
16 chr11:16175200-16177400 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
17 chr11:16175200-16177800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
18 chr11:16175200-16180600 Enhancers HMEC breast

Quick Search:


  
Input of quick search could be:

what's new

Quick links