Variant report

Variant rs993698
Chromosome Location chr11:16179325-16179326
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 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 chr11:16174800-16180000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr11:16175000-16180800 Enhancers NHEK skin
6 chr11:16175200-16180600 Enhancers HMEC breast
7 chr11:16177000-16180000 Weak transcription Hela-S3 cervix
8 chr11:16177200-16179800 Weak transcription Muscle Satellite Cultured Cells --
9 chr11:16177600-16181000 Enhancers A549 lung
10 chr11:16177600-16187800 Weak transcription Fetal Intestine Small intestine
11 chr11:16178000-16185200 Weak transcription Fetal Intestine Large intestine
12 chr11:16178800-16180800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
13 chr11:16179000-16180000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

Quick Search:


  
Input of quick search could be:

what's new

Quick links