Variant report

Variant rs4076445
Chromosome Location chr8:130706370-130706371
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:130699800-130706400 Flanking Active TSS K562 blood
2 chr8:130701600-130708400 Weak transcription Spleen Spleen
3 chr8:130701800-130707200 Enhancers Fetal Lung lung
4 chr8:130703800-130709600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr8:130704600-130706800 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
6 chr8:130705000-130708800 Weak transcription Osteobl bone
7 chr8:130705000-130709400 Weak transcription NHEK skin
8 chr8:130705000-130709600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr8:130705200-130709600 Weak transcription Muscle Satellite Cultured Cells --
10 chr8:130705400-130709800 Weak transcription Placenta Amnion Placenta Amnion
11 chr8:130705600-130708000 Weak transcription Esophagus oesophagus
12 chr8:130705600-130710000 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
13 chr8:130705800-130706800 Weak transcription A549 lung
14 chr8:130705800-130707000 Weak transcription Fetal Stomach stomach
15 chr8:130705800-130709800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
16 chr8:130705800-130709800 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
17 chr8:130705800-130713600 Weak transcription Fetal Adrenal Gland Adrenal Gland
18 chr8:130706000-130706400 Weak transcription Fetal Heart heart

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