Variant report

Variant rs192587
Chromosome Location chr1:165510068-165510069
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 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 chr1:165509000-165510200 Enhancers Breast Myoepithelial Primary Cells Breast
9 chr1:165509000-165510400 Enhancers Adipose Nuclei Adipose
10 chr1:165509000-165510400 Enhancers Right Atrium heart
11 chr1:165509000-165510600 Enhancers Psoas Muscle Psoas
12 chr1:165509400-165510400 Enhancers Brain Inferior Temporal Lobe brain
13 chr1:165509400-165510400 Enhancers Right Ventricle heart
14 chr1:165509600-165510600 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
15 chr1:165509600-165510600 Enhancers Skeletal Muscle Female skeletal muscle
16 chr1:165509800-165510200 Weak transcription Fetal Muscle Trunk muscle
17 chr1:165509800-165511400 Weak transcription Fetal Lung lung
18 chr1:165509800-165511800 Weak transcription Fetal Stomach stomach
19 chr1:165510000-165510200 Flanking Active TSS HSMMtube muscle
20 chr1:165510000-165510800 Enhancers Fetal Heart heart

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