Variant report

Variant rs285452
Chromosome Location chr1:165510771-165510772
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:165505600-165513000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr1:165507600-165512800 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
3 chr1:165508400-165510800 Enhancers Fetal Muscle Leg muscle
4 chr1:165508400-165510800 Enhancers Skeletal Muscle Male skeletal muscle
5 chr1:165509800-165511400 Weak transcription Fetal Lung lung
6 chr1:165509800-165511800 Weak transcription Fetal Stomach stomach
7 chr1:165510000-165510800 Enhancers Fetal Heart heart
8 chr1:165510200-165511000 Enhancers Fetal Muscle Trunk muscle
9 chr1:165510200-165513000 Weak transcription Breast Myoepithelial Primary Cells Breast
10 chr1:165510400-165512400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
11 chr1:165510400-165512800 Weak transcription Adipose Nuclei Adipose
12 chr1:165510400-165512800 Weak transcription Placenta Placenta
13 chr1:165510400-165512800 Weak transcription Right Atrium heart
14 chr1:165510400-165512800 Weak transcription Right Ventricle heart
15 chr1:165510400-165513000 Weak transcription Brain Inferior Temporal Lobe brain
16 chr1:165510600-165512000 Weak transcription Skeletal Muscle Female skeletal muscle
17 chr1:165510600-165512800 Weak transcription Left Ventricle heart
18 chr1:165510600-165512800 Weak transcription Psoas Muscle Psoas
19 chr1:165510600-165513000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin

Quick Search:


  
Input of quick search could be:

what's new

Quick links