Variant report

Variant rs1599955
Chromosome Location chr15:42348658-42348659
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr15:42341400-42348800 Weak transcription HUES6 Cell Line embryonic stem cell
2 chr15:42341400-42349000 Weak transcription Esophagus oesophagus
3 chr15:42342200-42349000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr15:42342400-42349000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr15:42343000-42349000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
6 chr15:42343000-42349000 Weak transcription Left Ventricle heart
7 chr15:42343000-42349000 Weak transcription Right Ventricle heart
8 chr15:42343000-42357600 Weak transcription Lung lung
9 chr15:42343800-42348800 Weak transcription Fetal Heart heart
10 chr15:42345600-42349000 Weak transcription Right Atrium heart
11 chr15:42345800-42349000 Weak transcription Pancreas Pancrea
12 chr15:42345800-42349000 Weak transcription Psoas Muscle Psoas
13 chr15:42346800-42348800 Weak transcription H1 Cell Line embryonic stem cell
14 chr15:42348200-42348800 Enhancers Breast Myoepithelial Primary Cells Breast
15 chr15:42348200-42349000 Enhancers Skeletal Muscle Female skeletal muscle
16 chr15:42348200-42349200 Bivalent Enhancer Fetal Muscle Leg muscle
17 chr15:42348400-42349000 Enhancers Skeletal Muscle Male skeletal muscle
18 chr15:42348600-42349000 Enhancers iPS-15b Cell Line embryonic stem cell

Quick Search:


  
Input of quick search could be:

what's new

Quick links