Variant report

Variant rs7761505
Chromosome Location chr6:162530432-162530433
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:162525200-162539800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr6:162529200-162530600 Enhancers Brain Inferior Temporal Lobe brain
3 chr6:162529800-162530600 Enhancers Left Ventricle heart
4 chr6:162529800-162530600 Enhancers Skeletal Muscle Male skeletal muscle
5 chr6:162529800-162530800 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
6 chr6:162529800-162531000 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
7 chr6:162530200-162530600 Enhancers Psoas Muscle Psoas
8 chr6:162530200-162531000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr6:162530200-162531000 Enhancers Muscle Satellite Cultured Cells --
10 chr6:162530200-162532600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
11 chr6:162530400-162530800 Enhancers HMEC breast
12 chr6:162530400-162530800 Enhancers HUVEC blood vessel
13 chr6:162530400-162530800 Enhancers NH-A brain
14 chr6:162530400-162530800 Enhancers NHDF-Ad bronchial
15 chr6:162530400-162531000 Enhancers Duodenum Smooth Muscle Duodenum
16 chr6:162530400-162531000 Enhancers Fetal Heart heart
17 chr6:162530400-162531000 Enhancers Skeletal Muscle Female skeletal muscle

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