Variant report

Variant rs927844
Chromosome Location chr1:165510312-165510313
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 chr1:165507600-165512800 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
4 chr1:165508400-165510800 Enhancers Fetal Muscle Leg muscle
5 chr1:165508400-165510800 Enhancers Skeletal Muscle Male skeletal muscle
6 chr1:165508600-165510400 Enhancers Placenta Placenta
7 chr1:165508600-165510600 Enhancers Left Ventricle heart
8 chr1:165509000-165510400 Enhancers Adipose Nuclei Adipose
9 chr1:165509000-165510400 Enhancers Right Atrium heart
10 chr1:165509000-165510600 Enhancers Psoas Muscle Psoas
11 chr1:165509400-165510400 Enhancers Brain Inferior Temporal Lobe brain
12 chr1:165509400-165510400 Enhancers Right Ventricle heart
13 chr1:165509600-165510600 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
14 chr1:165509600-165510600 Enhancers Skeletal Muscle Female skeletal muscle
15 chr1:165509800-165511400 Weak transcription Fetal Lung lung
16 chr1:165509800-165511800 Weak transcription Fetal Stomach stomach
17 chr1:165510000-165510800 Enhancers Fetal Heart heart
18 chr1:165510200-165511000 Enhancers Fetal Muscle Trunk muscle
19 chr1:165510200-165513000 Weak transcription Breast Myoepithelial Primary Cells Breast

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