Variant report

Variant rs7110987
Chromosome Location chr11:16176888-16176889
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:16172400-16191400 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 chr11:16174800-16178400 Enhancers Stomach Mucosa stomach
5 chr11:16174800-16180000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr11:16175000-16177000 Enhancers Hela-S3 cervix
7 chr11:16175000-16178400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr11:16175000-16180800 Enhancers NHEK skin
9 chr11:16175200-16177400 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
10 chr11:16175200-16177800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr11:16175200-16180600 Enhancers HMEC breast
12 chr11:16175400-16179000 Enhancers Pancreatic Islets Pancreatic Islet
13 chr11:16175600-16177600 Flanking Active TSS A549 lung
14 chr11:16175800-16177200 Enhancers Muscle Satellite Cultured Cells --
15 chr11:16176000-16177600 Enhancers Fetal Intestine Small intestine
16 chr11:16176200-16178000 Enhancers Fetal Intestine Large intestine
17 chr11:16176200-16178400 Enhancers HepG2 liver
18 chr11:16176800-16177200 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin

Quick Search:


  
Input of quick search could be:

what's new

Quick links