Variant report

Variant rs73131385
Chromosome Location chr5:92695871-92695872
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:92692200-92696800 Enhancers HMEC breast
2 chr5:92693600-92696000 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
3 chr5:92693600-92696200 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
4 chr5:92694600-92696000 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
5 chr5:92695000-92696600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr5:92695000-92697000 Enhancers HSMM muscle
7 chr5:92695200-92696000 Flanking Active TSS NHEK skin
8 chr5:92695200-92696400 Flanking Active TSS Muscle Satellite Cultured Cells --
9 chr5:92695400-92696000 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr5:92695600-92696000 Flanking Active TSS Hela-S3 cervix
11 chr5:92695600-92696000 Flanking Active TSS HUVEC blood vessel
12 chr5:92695600-92696000 Enhancers NH-A brain
13 chr5:92695600-92696800 Weak transcription Fetal Brain Male brain
14 chr5:92695800-92696400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
15 chr5:92695800-92696800 Weak transcription Fetal Adrenal Gland Adrenal Gland
16 chr5:92695800-92696800 Enhancers Osteobl bone

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