Variant report

Variant rs1326375
Chromosome Location chr1:165509350-165509351
allele A/C
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 chr1:165507200-165510400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
3 chr1:165507600-165509600 Weak transcription Cortex derived primary cultured neurospheres brain
4 chr1:165507600-165512800 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
5 chr1:165508400-165509400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
6 chr1:165508400-165510800 Enhancers Fetal Muscle Leg muscle
7 chr1:165508400-165510800 Enhancers Skeletal Muscle Male skeletal muscle
8 chr1:165508600-165509800 Enhancers Aorta Aorta
9 chr1:165508600-165509800 Enhancers Fetal Muscle Trunk muscle
10 chr1:165508600-165510400 Enhancers Placenta Placenta
11 chr1:165508600-165510600 Enhancers Left Ventricle heart
12 chr1:165508800-165509600 Enhancers Fetal Heart heart
13 chr1:165509000-165509400 Weak transcription Right Ventricle heart
14 chr1:165509000-165510000 Enhancers HSMMtube muscle
15 chr1:165509000-165510200 Enhancers Breast Myoepithelial Primary Cells Breast
16 chr1:165509000-165510400 Enhancers Adipose Nuclei Adipose
17 chr1:165509000-165510400 Enhancers Right Atrium heart
18 chr1:165509000-165510600 Enhancers Psoas Muscle Psoas
19 chr1:165509200-165509600 Flanking Active TSS Skeletal Muscle Female skeletal muscle

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