Variant report

Variant rs16984680
Chromosome Location chr20:22842538-22842539
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr20:22841000-22844600 Weak transcription Right Atrium heart
2 chr20:22841400-22843000 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
3 chr20:22841600-22843000 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
4 chr20:22841600-22843200 Enhancers NHDF-Ad bronchial
5 chr20:22841600-22843400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
6 chr20:22841800-22843200 Enhancers NHEK skin
7 chr20:22841800-22843400 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
8 chr20:22841800-22844600 Weak transcription Spleen Spleen
9 chr20:22842000-22843000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr20:22842000-22845000 Enhancers Fetal Muscle Leg muscle
11 chr20:22842200-22842800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr20:22842200-22842800 Enhancers HSMM muscle
13 chr20:22842200-22843200 Enhancers Fetal Adrenal Gland Adrenal Gland
14 chr20:22842200-22843200 Flanking Active TSS HUVEC blood vessel

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