Variant report

Variant rs182146847
Chromosome Location chr6:150814375-150814376
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:150811200-150815800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr6:150811400-150814800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr6:150811400-150815000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr6:150811400-150815200 Enhancers Fetal Muscle Leg muscle
5 chr6:150812000-150814800 Enhancers NH-A brain
6 chr6:150812400-150814800 Enhancers HUVEC blood vessel
7 chr6:150813200-150815200 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
8 chr6:150813400-150814600 Flanking Active TSS HMEC breast
9 chr6:150813800-150814400 Enhancers Fetal Muscle Trunk muscle
10 chr6:150813800-150814400 Enhancers Pancreas Pancrea
11 chr6:150813800-150814800 Enhancers Fetal Adrenal Gland Adrenal Gland
12 chr6:150813800-150815200 Enhancers Right Ventricle heart
13 chr6:150813800-150815200 Enhancers Skeletal Muscle Male skeletal muscle
14 chr6:150814000-150814400 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
15 chr6:150814000-150814400 Enhancers Colon Smooth Muscle Colon
16 chr6:150814200-150814800 Enhancers NHEK skin
17 chr6:150814200-150815000 Weak transcription Left Ventricle heart
18 chr6:150814200-150815600 Enhancers Adipose Nuclei Adipose

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